Control of Hazardous Air Pollutants From Mobile Sources, 15804-15963 [06-2315]
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15804
Federal Register / Vol. 71, No. 60 / Wednesday, March 29, 2006 / Proposed Rules
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Parts 59, 80, 85 and 86
[EPA–HQ–OAR–2005–0036; FRL–8041–2]
RIN 2060–AK70
Control of Hazardous Air Pollutants
From Mobile Sources
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
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AGENCY:
SUMMARY: Today EPA is proposing
controls on gasoline, passenger vehicles,
and portable gasoline containers (gas
cans) that would significantly reduce
emissions of benzene and other
hazardous air pollutants (‘‘mobile
source air toxics’’). Benzene is a known
human carcinogen, and mobile sources
are responsible for the majority of
benzene emissions. The other mobile
source air toxics are known or suspected
to cause cancer or other serious health
effects.
We are proposing to limit the benzene
content of gasoline to an annual average
of 0.62% by volume, beginning in 2011.
We are also proposing to limit exhaust
emissions of hydrocarbons from
passenger vehicles when they are
operated at cold temperatures. This
standard would be phased in from 2010
to 2015. For passenger vehicles we also
propose evaporative emissions
standards that are equivalent to those in
California. Finally, we are proposing a
hydrocarbon emissions standard for gas
cans beginning in 2009, which would
reduce evaporation and spillage of
gasoline from these containers.
These controls would significantly
reduce emissions of benzene and other
mobile source air toxics such as 1,3butadiene, formaldehyde, acetaldehyde,
acrolein, and naphthalene. This
proposal would result in additional
substantial benefits to public health and
welfare by significantly reducing
emissions of particulate matter from
passenger vehicles.
We project annual nationwide
benzene reductions of 35,000 tons in
2015, increasing to 65,000 tons by 2030.
Total reductions in mobile source air
toxics would be 147,000 tons in 2015
and over 350,000 tons in 2030.
Passenger vehicles in 2030 would emit
45% less benzene. Gas cans meeting the
new standards would emit almost 80%
less benzene. Gasoline would have 37%
less benzene overall. We estimate that
these reductions would have an average
cost of less than 1 cent per gallon of
gasoline and less than $1 per vehicle.
The average cost for gas cans would be
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less than $2 per can. The reduced
evaporation from gas cans would result
in significant fuel savings, which would
more than offset the increased cost for
the gas can.
DATES: Comments must be received on
or before May 30, 2006. Under the
Paperwork Reduction Act, comments on
the information collection provisions
must be received by OMB on or before
April 28, 2006.
Hearing: We will hold a public
hearing on April 12, 2006. The hearing
will start at 10 a.m. local time and
continue until everyone has had a
chance to speak. If you want to testify
at the hearing, notify the contact person
listed under FOR FURTHER INFORMATION
CONTACT by April 3, 2006.
ADDRESSES: Submit your comments,
identified by Docket ID No. EPA–HQ–
OAR–2005–0036, by one of the
following methods:
• https://www.regulations.gov: Follow
the on-line instructions for submitting
comments.
• Fax your comments to: (202) 566–
1741.
• Mail: Air Docket, Environmental
Protection Agency, Mailcode: 6102T,
1200 Pennsylvania Ave., NW.,
Washington, DC 20460. In addition,
please mail a copy of your comments on
the information collection provisions to
the Office of Information and Regulatory
Affairs, Office of Management and
Budget (OMB), Attn: Desk Officer for
EPA, 725 17th St. NW., Washington, DC
20503.
• Hand Delivery: EPA Docket Center,
(EPA/DC) EPA West, Room B102, 1301
Constitution Ave., NW., Washington,
DC 20004. Such deliveries are only
accepted during the Docket’s normal
hours of operation, and special
arrangements should be made for
deliveries of boxed information.
Instructions: Direct your comments to
Docket ID No. EPA–HQ–OAR–2005–
0036. EPA’s policy is that all comments
received will be included in the public
docket without change and may be
made available online at
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through www.regulations.gov
or e-mail. The www.regulations.gov
website is an ‘‘anonymous access’’
system, which means EPA will not
know your identity or contact
information unless you provide it in the
body of your comment. If you send an
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e-mail comment directly to EPA without
going through www.regulations.gov your
e-mail address will be automatically
captured and included as part of the
comment that is placed in the public
docket and made available on the
Internet. If you submit an electronic
comment, EPA recommends that you
include your name and other contact
information in the body of your
comment and with any disk or CD–ROM
you submit. If EPA cannot read your
comment due to technical difficulties
and cannot contact you for clarification,
EPA may not be able to consider your
comment. Electronic files should avoid
the use of special characters, any form
of encryption, and be free of any defects
or viruses. For additional information
about EPA’s public docket visit the EPA
Docket Center homepage at https://
www.epa.gov/epahome/dockets.htm.
For additional instructions on
submitting comments, go to section XI,
Public Participation, of the
SUPPLEMENTARY INFORMATION section of
this document.
Docket: All documents in the docket
are listed in the www.regulations.gov
index. Although listed in the index,
some information is not publicly
available, e.g., CBI or other information
whose disclosure is restricted by statute.
Certain other material, such as
copyrighted material, will be publicly
available only in hard copy. Publicly
available docket materials are available
either electronically in
www.regulations.gov or in hard copy at
the Air Docket, EPA/DC, EPA West,
Room B102, 1301 Constitution Ave.,
NW., Washington, DC. The Public
Reading Room is open from 8:30 a.m. to
4:30 p.m., Monday through Friday,
excluding legal holidays. The telephone
number for the Public Reading Room is
(202) 566–1744, and the telephone
number for the Air Docket is (202) 566–
1742.
Hearing: The public hearing will be
held at Sheraton Crystal City Hotel,
1800 Jefferson Davis Highway,
Arlington, Virginia 22202, Telephone:
(703) 486–1111. See section XI, Public
Participation, for more information
about public hearings.
Mr.
Chris Lieske, U.S. EPA, Office of
Transportation and Air Quality,
Assessment and Standards Division
(ASD), Environmental Protection
Agency, 2000 Traverwood Drive, Ann
Arbor, MI 48105; telephone number:
(734) 214–4584; fax number: (734) 214–
4816; email address:
lieske.christopher@epa.gov, or
Assessment and Standards Division
FOR FURTHER INFORMATION CONTACT:
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Hotline; telephone number: (734) 214–
4636; e-mail address: asdinfo@epa.gov.
SUPPLEMENTARY INFORMATION:
General Information
A. Does this Action Apply to Me?
Entities potentially affected by this
action are those that produce new motor
vehicles, alter individual imported
motor vehicles to address U.S.
NAICS
codes a
Category
Industry ................................................................................................
Industry ................................................................................................
336111
335312
424720
811198
Industry ................................................................................................
SIC
codes b
811111
811112
811198
324110
326199
332431
Industry ................................................................................................
Industry ................................................................................................
a North
3711
3621
5172
7539
7549
7538
7533
7549
2911
3089
3411
15805
regulation, or convert motor vehicles to
use alternative fuels. It would also affect
you if you produce gasoline motor fuel
or manufacture portable gasoline
containers. Regulated categories
include:
Examples of potentially affected entities
Motor vehicle manufacturers.
Alternative fuel vehicle converters.
Independent commercial importers.
Gasoline fuel refiners.
Portable fuel container manufacturers.
American Industry Classification System (NAICS).
Industrial Classification (SIC) system code.
b Standard
This table is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
regulated by this action. This table lists
the types of entities that EPA is now
aware could potentially be regulated by
this action. Other types of entities not
listed in the table could also be
regulated. To determine whether your
activities are regulated by this action,
you should carefully examine the
applicability criteria in 40 CFR parts 59,
80, 85, and 86. If you have any
questions regarding the applicability of
this action to a particular entity, consult
the person listed in the preceding FOR
FURTHER INFORMATION CONTACT section.
B. What Should I Consider as I Prepare
My Comments for EPA?
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1. Submitting CBI
Do not submit this information to EPA
through www.regulations.gov or e-mail.
Clearly mark the part or all of the
information that you claim to be
confidential business information (CBI).
For CBI information in a disk or CD
ROM that you mail to EPA, mark the
outside of the disk or CD ROM as CBI
and then identify electronically within
the disk or CD ROM the specific
information that is claimed as CBI. In
addition to one complete version of the
comment that includes information
claimed as CBI, a copy of the comment
that does not contain the information
claimed as CBI must be submitted for
inclusion in the public docket.
Information so marked will not be
disclosed except in accordance with
procedures set forth in 40 CFR part 2.
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2. Tips for Preparing Your Comments
When submitting comments,
remember to:
• Explain your views as clearly as
possible.
• Describe any assumptions that you
used.
• Provide any technical information
and/or data you used that support your
views.
• If you estimate potential burden or
costs, explain how you arrived at your
estimate.
• Provide specific examples to
illustrate your concerns.
• Offer alternatives.
• Make sure to submit your
comments by the comment period
deadline identified.
• To ensure proper receipt by EPA,
identify the appropriate docket
identification number in the subject line
on the first page of your response. It
would also be helpful if you provided
the name, date, and Federal Register
citation related to your comments.
Outline of This Preamble
I. Introduction
A. Summary
B. What Background Information is Helpful
to Understand this Proposal?
1. What Are Air Toxics and Related Health
Effects?
2. What is the Statutory Authority for
Today’s Proposal?
a. Clean Air Act Section 202(l)
b. Clean Air Act Section 183(e)
c. Energy Policy Act
3. What Other Actions Has EPA Taken
Under Clean Air Act Section 202(l)?
a. 2001 Mobile Source Air Toxics Rule
b. Technical Analysis Plan
II. Overview of Proposal
A. Why Is EPA Making This Proposal?
1. National Cancer Risk from Air Toxics
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2. Noncancer Health Effects
3. Exposure Near Roads and From
Attached Garages
4. Ozone and Particulate Matter
B. What Is EPA Proposing?
1. Light-Duty Vehicle Emission Standards
2. Gasoline Fuel Standards
3. Portable Gasoline Container (Gas Can)
Controls
III. What Are Mobile Source Air Toxics
(MSATs) and Their Health Effects?
A. What Are MSATs?
B. Compounds Emitted by Mobile Sources
and Identified in IRIS
C. Which Mobile Source Emissions Pose
the Greatest Health Risk at Current
Levels?
1. National and Regional Risk Drivers in
1999 National-Scale Air Toxics
Assessment
2. 1999 NATA Risk Drivers with
Significant Mobile Source Contribution
D. What Are the Health Effects of Air
Toxics?
1. Overview of Potential Cancer and
Noncancer Health Effects
2. Health Effects of Key MSATs
a. Benzene
b. 1,3-Butadiene
c. Formaldehyde
d. Acetaldehyde
e. Acrolein
f. Polycyclic Organic Matter (POM)
g. Naphthalene
h. Diesel Particulate Matter and Diesel
Exhaust Organic Gases
E. Gasoline PM
F. Near-Roadway Health Effects
G. How Would This Proposal Reduce
Emissions of MSATs?
IV. What Are the Air Quality and Health
Impacts of Air Toxics, and How do
Mobile Sources Contribute?
A. What Is the Health Risk to the U.S.
Population from Inhalation Exposure to
Ambient Sources of Air Toxics, and How
Would It be Reduced by the Proposed
Controls?
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B. What is the Distribution of Exposure and
Risk?
1. Distribution of National-Scale Estimates
of Risk from Air Toxics
2. Elevated Concentrations and Exposure
in Mobile Source-Impacted Areas
a. Concentrations Near Major Roadways
b. Exposures Near Major Roadways
i. Vehicles
ii. Homes and Schools
iii. Pedestrians and Bicyclists
c. Exposure and Concentrations in Homes
with Attached Garages
d. Occupational Exposure
3. What Are the Size and Characteristics of
Highly Exposed Populations?
4. What Are the Implications for
Distribution of Individual Risk?
C. Ozone
1. Background
2. Health Effects of Ozone
3. Current and Projected 8-hour Ozone
Levels
D. Particulate Matter
1. Background
2. Health Effects of PM
3. Current and Projected PM2.5 Levels
4. Current PM10 Levels
E. Other Environmental Effects
1. Visibility
a. Background
b. Current Visibility Impairment
c. Future Visibility Impairment
2. Plant Damage from Ozone
3. Atmospheric Deposition
4. Materials Damage and Soiling
V. What Are Mobile Source Emissions Over
Time and How Would This Proposal
Reduce Emissions, Exposure and
Associated Health Effects?
A. Mobile Source Contribution to Air
Toxics Emissions
B. VOC Emissions from Mobile Sources
C. PM Emissions from Mobile Sources
D. Description of Current Mobile Source
Emissions Control Programs that Reduce
MSATs
1. Fuels Programs
a. RFG
b. Anti-dumping
c. 2001 Mobile Source Air Toxics Rule
(MSAT1)
d. Gasoline Sulfur
e. Gasoline Volatility
f. Diesel Fuel
g. Phase-Out of Lead in Gasoline
2. Highway Vehicle and Engine Programs
3. Nonroad Engine Programs
4. Voluntary Programs
E. Emission Reductions from Proposed
Controls
1. Proposed Vehicle Controls
a. Volatile Organic Compounds (VOC)
b. Toxics
c. PM2.5
2. Proposed Fuel Benzene Controls
3. Proposed Gas Can Standards
a. VOC
b. Toxics
4. Total Emission Reductions from
Proposed Controls
a. Toxics
b. VOC
c. PM2.5
F. How Would This Proposal Reduce
Exposure to Mobile Source Air Toxics
and Associated Health Effects?
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G. Additional Programs Under
Development That Will Reduce MSATs
1. On-Board Diagnostics for Heavy-Duty
Vehicles Over 14,000 Pounds
2. Standards for Small SI Engines
3. Standards for Locomotive and Marine
Engines
VI. Proposed New Light-duty Vehicle
Standards
A. Why are We Proposing New Standards?
1. The Clean Air Act and Air Quality
2. Technology Opportunities for Light-Duty
Vehicles
3. Cold Temperature Effects on Emission
Levels
a. How Does Temperature Affect
Emissions?
b. What Are the Current Emissions Control
Requirements?
c. Opportunities for Additional Control
B. What Cold Temperature Requirements
Are We Proposing?
1. NMHC Exhaust Emissions Standards
2. Feasibility of the Proposed Standards
a. Currently Available Emission Control
Technologies
b. Feasibility Considering Current
Certification Levels, Deterioration and
Compliance Margin
c. Feasibility and Test Programs for Higher
Weight Vehicles
3. Standards Timing and Phase-in
a. Phase-In Schedule
b. Alternative Phase-In Schedules
4. Certification Levels
5. Credit Program
a. How Credits Are Calculated
b. Credits Earned Prior to Primary PhaseIn Schedule
c. How Credits Can Be Used
d. Discounting and Unlimited Life
e. Deficits Could Be Carried Forward
f. Voluntary Heavy-Duty Vehicle Credit
Program
6. Additional Vehicle Cold Temperature
Standard Provisions
a. Applicability
b. Useful Life
c. High Altitude
d. In-Use Standards for Vehicles Produced
During Phase-in
7. Monitoring and Enforcement
C. What Evaporative Emissions Standards
Are We Proposing?
1. Current Controls and Feasibility of the
Proposed Standards
2. Evaporative Standards Timing
3. Timing for Multi-Fueled Vehicles
4. In-Use Evaporative Emission Standards
5. Existing Differences Between California
and Federal Evaporative Emission Test
Procedures
D. Opportunities for Additional Exhaust
Control Under Normal Conditions
E. Vehicle Provisions for Small Volume
Manufacturers
1. Lead Time Transition Provisions
2. Hardship Provisions
3. Special Provisions for Independent
Commercial Importers (ICIs)
VII. Proposed Gasoline Benzene Control
Program
A. Overview of Today’s Proposed Fuel
Control Program
B. Description of the Proposed Fuel
Control Program
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C. Development of the Proposed Gasoline
Benzene Standard
1. Why Are We Focusing on Controlling
Benzene Emissions?
a. Other MSAT Emissions
b. MSAT Emission Reductions Through
Lowering Gasoline Volatility or Sulfur
Content
i. Gasoline Sulfur Content
ii. Gasoline Vapor Pressure
c. Toxics Performance Standard
d. Diesel Fuel Changes
2. Why Are We Proposing To Control
Benzene Emissions By Controlling
Gasoline Benzene Content?
a. Benzene Content Standard
b. Gasoline Aromatics Content Standard
c. Benzene Emission Standard
3. How Did We Select the Level of the
Proposed Gasoline Benzene Content
Standard?
a. Current Gasoline Benzene Levels
b. The Need for an Average Benzene
Standard
c. Potential Levels for the Average Benzene
Standard
d. Comparison of Other Benzene
Regulatory Programs
4. How Do We Address Variations in
Refinery Benzene Levels?
a. Overall Reduction in Benzene Level and
Variation
b. Consideration of an Upper Limit
Standard
i. Per-Gallon Cap Standard
ii. Maximum Average Standard
5. How Would the Proposed Program Meet
or Exceed Related Statutory and
Regulatory Requirements?
D. Description of the Proposed Averaging,
Banking, and Trading (ABT) Program
1. Overview
2. Standard Credit Generation (2011 and
Beyond)
3. Credit Use
a. Credit Trading Area
b. Credit Life
4. Early Credit Generation (2007–2010)
a. Establishing Early Credit Baselines
b. Early Credit Reduction Criteria (Trigger
Points)
c. Calculating Early Credits
5. Additional Credit Provisions
a. Credit Trading
b. Pre-Compliance Reporting Requirements
6. Special ABT Provisions for Small
Refiners
E. Regulatory Flexibility Provisions for
Qualifying Refiners
1. Hardship Provisions for Qualifying
Small Refiners
a. Qualifying Small Refiners
i. Regulatory Flexibility for Small Refiners
ii. Rationale for Small Refiner Provisions
b. How Do We Propose to Define Small
Refiners for the Purpose of the Hardship
Provisions?
c. What Options Would Be Available For
Small Refiners?
i. Delay in Standards
ii. ABT Credit Generation Opportunities
iii. Extended Credit Life
iv. ABT Program Review
d. How Would Refiners Apply for Small
Refiner Status?
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e. The Effect of Financial and Other
Transactions on Small Refiner Status and
Small Refiner Relief Provisions
2. General Hardship Provisions
a. Temporary Waivers Based on
Unforeseen Circumstances
b. Temporary Waivers Based on Extreme
Hardship Circumstances
c. Early Compliance with the Proposed
Benzene Standard
F. Technological Feasibility of Gasoline
Benzene Reduction
1. Benzene Levels in Gasoline
2. Technologies for Reducing Gasoline
Benzene Levels
a. Why is Benzene Found in Gasoline?
b. Benzene Control Technologies Related to
the Reformer
i. Routing Around the Reformer
ii. Routing to the Isomerization Unit
iii. Benzene Saturation
iv. Benzene Extraction
c. Other Benzene Reduction Technologies
d. Impacts on Octane and Strategies for
Recovering Octane Loss
e. Experience Using Benzene Control
Technologies
f. What Are the Potential Impacts of
Benzene Control on Other Fuel
Properties?
3. Feasible Level of Benzene Control
4. Lead time
5. Issues
a. Small Refiners
b. Imported Gasoline
G. How Does the Proposed Fuel Control
Program Satisfy the Statutory
Requirements?
H. Effect on Energy Supply, Distribution,
or Use
I. How Would the Proposed Gasoline
Benzene Standard Be Implemented?
1. General provisions
a. What Are the Implementation Dates for
the Proposed Program?
b. Which Regulated Parties Would Be
Subject to the Proposed Benzene
Standards?
c. What Gasoline Would Be Subject to the
Proposed Benzene Standards?
d. How Would Compliance With the
Benzene Standard Be Determined?
2. Averaging, Banking and Trading
Program
a. Early Credit Generation
b. How Would Refinery Benzene Baselines
Be Determined?
c. Credit Generation Beginning in 2011
d. How Would Credits Be Used?
3. Hardship and Small Refiner Provisions
a. Hardship
b. Small Refiners
4. Administrative and Enforcement Related
Provisions
a. Sampling/Testing
b. Recordkeeping/Reporting
c. Attest Engagements, Violations,
Penalties
5. How Would Compliance With the
Provisions of the Proposed Benzene
Program Affect Compliance With Other
Gasoline Toxics Programs?
VIII. Gas Cans
A. Why Are We Proposing an Emissions
Control Program for Gas Cans?
1. VOC Emissions
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2. Technological Opportunities to Reduce
Emissions from Gas Cans
3. State Experiences Regulating Gas Cans
B. What Emissions Standard is EPA
Proposing, and Why?
1. Description of Emissions Standard
2. Determination of Best Available Control
3. Emissions Performance vs. Design
Standard
4. Automatic Shut-Off
5. Consideration of Retrofits of Existing Gas
Cans
6. Consideration of Diesel, Kerosene and
Utility Containers
C. Timing of Standard
D. What Test Procedures Would Be Used?
1. Diurnal Test
2. Preconditioning to Ensure Durable InUse Control
a. Durability cycles
b. Preconditioning Fuel Soak
c. Spout Actuation
E. What Certification and In-Use
Compliance Provisions Is EPA
Proposing?
1. Certification
2. Emissions Warranty and In-Use
Compliance
3. Labeling
F. How Would State Programs Be Affected
By EPA Standards?
G. Provisions for Small Gas Can
Manufacturers
1. First Type of Hardship Provision
2. Second Type of Hardship Provision
IX. What are the Estimated Impacts of the
Proposal?
A. Refinery Costs of Gasoline Benzene
Reduction
1. Tools and Methodology
a. Linear Programming Cost Model
b. Refiner-by-Refinery Cost Model
c. Price of Chemical Grade Benzene
d. Applying the Cost Model to Special
Cases
2. Summary of Costs
a. Nationwide Costs of the Proposed
Program
b. Regional Distribution of Costs
c. Cost Effects of Different Standards
d. Effect on Cost Estimates of Higher
Benzene Prices
3. Economic Impacts of MSAT Control
Through Gasoline Sulfur and RVP
Control and a Total Toxics Standard
B. What Are the Vehicle Cost Impacts?
C. What Are The Gas Can Cost Impacts?
D. Cost Per Ton of Emissions Reduced
E. Benefits
1. Unquantified Health and Environmental
Benefits
2. Quantified Human Health and
Environmental Effects of the Proposed
Cold Temperature Vehicle Standard
3. Monetized Benefits
4. What Are the Significant Limitations of
the Benefit Analysis?
5. How Do the Benefits Compare to the
Costs of The Proposed Standards?
F. Economic Impact Analysis
1. What Is an Economic Impact Analysis?
2. What Is the Economic Impact Model?
3. What Economic Sectors Are Included in
this Economic Impact Analysis?
4. What Are the Key Features of the
Economic Impact Model?
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5. What Are the Key Model Inputs?
6. What Are the Results of the Economic
Impact Modeling?
X. Alternative Program Options
A. Fuels
B. Vehicles
C. Gas cans
XI. Public Participation
A. How Do I Submit Comments?
B. How Should I Submit CBI to the
Agency?
C. Will There Be a Public Hearing?
D. Comment Period
E. What Should I Consider as I Prepare My
Comments for EPA?
XII. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory
Planning and Review
B. Paperwork Reduction Act
C. Regulatory Flexibility Act (RFA), as
amended by the Small Business
Regulatory Enforcement Fairness Act of
1996 (SBREFA), 5 U.S.C. 601 et. seq
1. Overview
2. Background
3. Summary of Regulated Small Entities
a. Highway Light-Duty Vehicles
b. Gasoline Refiners
c. Portable Gasoline Container
Manufacturers
4. Potential Reporting, Record Keeping,
and Compliance
5. Relevant Federal Rules
6. Summary of SBREFA Panel Process and
Panel Outreach
a. Significant Panel Findings
b. Panel Process
c. Small Business Flexibilities
i. Highway Light-Duty Vehicles
(a) Highway Light-Duty Vehicle
Flexibilities
(b) Highway Light-Duty Vehicle Hardships
ii. Gasoline Refiners
(a) Gasoline Refiner Flexibilities
(b) Gasoline Refiner Hardships
iii. Portable Gasoline Containers
(a) Portable Gasoline Container
Flexibilities
(b) Portable Gasoline Container Hardships
D. Unfunded Mandates Reform Act
E. Executive Order 13132: Federalism
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
G. Executive Order 13045: Protection of
Children from Environmental Health and
Safety Risks
H. Executive Order 13211: Actions that
Significantly Affect Energy Supply,
Distribution, or Use
I. National Technology Transfer
Advancement Act
J. Executive Order 12898: Federal Actions
To Address Environmental Justice in
Minority Populations and Low-Income
Populations
XIII. Statutory Provisions and Legal
Authority
I. Introduction
A. Summary
Mobile sources emit air toxics that
can cause cancer and other serious
health effects. Section III of this
preamble and Chapter 1 of the
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Regulatory Impact Analysis (RIA) for
this rule describe these compounds and
their health effects. Mobile sources
contribute significantly to the
nationwide risk from breathing outdoor
sources of air toxics. Mobile sources
were responsible for about 44% of
outdoor toxic emissions, almost 50% of
the cancer risk, and 74% of the
noncancer risk according to EPA’s
National-Scale Air Toxics Assessment
(NATA) for 1999. In addition, people
who live or work near major roads or
live in homes with attached garages are
likely to have higher exposures and risk,
which are not reflected in NATA.
Sections II.A and IV of this preamble
and Chapter 3 of the RIA provide more
detail about NATA, as well as our
analysis of exposures near roadways.
According to NATA for 1999, there
are a few mobile source air toxics that
pose the greatest risk based on current
information about ambient levels and
exposure. These include benzene, 1,3butadiene, formaldehyde, acrolein,
naphthalene, and polycyclic organic
matter (POM). All of these compounds
are hydrocarbons except POM. Benzene
is the most significant contributor to
cancer risk from all outdoor air toxics,
according to NATA for 1999. NATA
does not include a quantitative estimate
of cancer risk for diesel exhaust, but it
concludes that diesel exhaust
(specifically, diesel particulate matter
and diesel exhaust organic gases) is one
of the pollutants that pose the greatest
relative cancer risk. Although we expect
significant reductions in mobile source
air toxics in the future, cancer and
noncancer health risks will remain a
public health concern, and exposure to
benzene will remain the largest
contributor to this risk.
As discussed in detail in Section V of
this preamble and Chapter 2 of the RIA,
this proposal would significantly reduce
emissions of the many air toxics that are
hydrocarbons, including benzene, 1,3butadiene, formaldehyde, acetaldehyde,
acrolein, and naphthalene. The
proposed fuel benzene standard and
hydrocarbon standards for vehicles and
gas cans would together reduce total
emissions of mobile source air toxics by
350,000 tons in 2030, including 65,000
tons of benzene. Mobile sources were
responsible for 68% of benzene
emissions in 1999. As a result of this
proposal, in 2030 passenger vehicles
would emit 45% less benzene, gas cans
would emit 78% less benzene, and the
gasoline would have 37% less benzene
overall.
In addition, EPA has already taken
significant steps to reduce diesel
emissions from mobile sources, which
will result in a 70% reduction between
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1999 and 2020. We have adopted
stringent standards for diesel trucks and
buses, and nonroad diesel engines
(engines used, for example, in
construction, agricultural, and
industrial applications). We also have
additional programs underway to
reduce diesel emissions, including
voluntary programs and a proposal that
is being developed to reduce emissions
from diesel locomotives and marine
engines.
The proposed reductions in mobile
source air toxics emissions would
reduce exposure and predicted risk of
cancer and noncancer health effects,
including in environments where
exposure and risk may be highest, such
as near roads, in vehicles, and in homes
with attached garages. In addition, the
hydrocarbon reductions from the
vehicle and gas can standards would
reduce VOC emissions (which are a
precursor to ozone and PM2.5) by over 1
million tons in 2030. The proposed
vehicle standards would reduce direct
PM2.5 emissions by 20,000 tons in 2030
and would also reduce secondary
formation of PM2.5. Although ozone and
PM2.5 are considered criteria pollutants
rather than ‘‘air toxics,’’ reductions in
ozone and PM2.5 are important cobenefits of this proposal. More details
on emissions, cancer risks, and adverse
health and welfare effects associated
with ozone and PM are found in
sections II.A, IV and V of this preamble
and Chapters 2 and 3 of the RIA.
Section II.B of this preamble provides
an overview of the regulatory program
that EPA is proposing for passenger
vehicles, gasoline, and gas cans. We are
proposing standards to limit the exhaust
hydrocarbons from passenger vehicles
during cold temperature operation. We
are also proposing evaporative
hydrocarbon emissions standards for
passenger vehicles. We are proposing to
limit the average annual benzene
content of gasoline. Finally, we are
proposing hydrocarbon emissions
standards for gas cans that would
reduce evaporation, permeation, and
spillage from these containers. Detailed
discussion of each of these programs is
in sections VI, VII, and VIII of the
preamble and Chapters 5, 6, and 7 of the
RIA.
We estimate that the benefits of this
proposal would be about $6 billion in
2030, based on the direct PM2.5
reductions from the vehicle standards,
plus unquantified benefits from
reductions in mobile source air toxics
and VOC. We estimate that the annual
net social costs of this proposal would
be about $200 million in 2030
(expressed in 2003 dollars). These net
social costs include the value of fuel
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savings from the proposed gas can
standards, which would be worth $82
million in 2030.
The proposed reductions would have
an average cost of 0.13 cents per gallon
of gasoline, less than $1 per vehicle, and
less than $2 per gas can. The reduced
evaporation from gas cans would result
in fuel savings that would more than
offset the increased cost for the gas can.
In 2030, the long-term cost per ton of
the proposed standards (in combination,
and including fuel savings) would be
$450 per ton of total mobile source air
toxics reduced; $2,400 per ton of
benzene reduced; and no cost for the
hydrocarbon and PM reductions
(because the vehicle standards would
have no cost in 2020 and beyond).
Section IX of the preamble and Chapters
8–13 of the RIA provide more details on
the costs, benefits, and economic
impacts of the proposed standards. The
impacts on small entities and the
flexibilities we are proposing are
discussed in section XII.C of this
preamble and Chapter 14 of the RIA.
B. What Background Information is
Helpful to Understand this Proposal?
1. What Are Air Toxics and Related
Health Effects?
Air toxics, which are also known in
the Clean Air Act as ‘‘hazardous air
pollutants,’’ are those pollutants known
or suspected to cause cancer or other
serious health or environmental effects.
For example, some of these pollutants
are known to have negative effects on
people’s respiratory, cardiovascular,
neurological, immune, reproductive, or
other organ systems, and they may also
have developmental effects. They may
pose particular hazards to more
susceptible and sensitive populations,
such as children, the elderly, or people
with pre-existing illnesses.
Mobile source air toxics (MSATs) are
those toxics emitted by motor vehicles,
nonroad engines (such as lawn and
garden equipment, farming and
construction equipment, aircraft,
locomotives, and ships), and their fuels.
Toxics are also emitted by stationary
sources such as power plants, factories,
oil refineries, dry cleaners, gas stations,
and small manufacturers. They can also
be produced by combustion of wood
and other organic materials. There are
also indoor sources of air toxics, such as
solvent evaporation and outgassing from
furniture and building materials.
Some MSATs of particular concern
include benzene, 1,3-butadiene,
formaldehyde, acrolein, naphthalene,
and diesel particulate matter and diesel
exhaust organic gases. Benzene and 1,3butadiene are both known human
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carcinogens. Section III of this preamble
provides more detail on the health
effects of each of these pollutants.
MSATs are emitted as a result of
various processes. Some MSATs are
present in fuel or fuel additives and are
emitted to the air when the fuel
evaporates or passes through the engine.
Some MSATs are formed through
engine combustion processes. Some
compounds, like formaldehyde and
acetaldehyde, are also formed through a
secondary process when other mobile
source pollutants undergo chemical
reactions in the atmosphere. Finally,
some air toxics, such as metals, result
from engine wear or from impurities in
oil or fuel.
2. What is the Statutory Authority for
Today’s Proposal?
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a. Clean Air Act Section 202(l)
Section 202(l)(2) of the Clean Air Act
requires EPA to set standards to control
hazardous air pollutants from motor
vehicles, motor vehicle fuels, or both.
These standards must reflect the greatest
degree of emission reduction achievable
through the application of technology
which will be available, taking into
consideration the motor vehicle
standards established under section
202(a) of the Act, the availability and
cost of the technology, and noise, energy
and safety factors, and lead time. The
standards are to be set under Clean Air
Act sections 202(a)(1) or 211(c)(1), and
they are to apply, at a minimum, to
benzene and formaldehyde emissions.
Section 202(a)(1) of the Clean Air Act
directs EPA to set standards for new
motor vehicles or new motor vehicle
engines which EPA judges to cause or
contribute to air pollution which may
reasonably be anticipated to endanger
public health or welfare. We are
proposing a cold-temperature
hydrocarbon emission standard for
passenger vehicles under this authority.
Section 211(c)(1)(A) of the Clean Air
Act authorizes EPA (among other
things) to control the manufacture of
fuel if any emission product of such fuel
causes or contributes to air pollution
which may reasonably be anticipated to
endanger public health or welfare. We
are proposing a benzene standard for
gasoline under this authority.
Clean Air Act section 202(l)(2)
requires EPA to ‘‘from time to time
revise’’ its regulations controlling
hazardous air pollutants from motor
vehicles and fuels. As described in more
detail in section I.F. below, EPA has
previously set standards under section
202(l), and we committed in that rule to
engage in further rulemaking to
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implement section 202(l). This proposal
fulfills that commitment.
b. Clean Air Act Section 183(e)
Clean Air Act section 183(e)(3)
requires EPA to list categories of
consumer or commercial products that
the Administrator determines, based on
an EPA study of VOC emissions from
such products, contribute at least 80
percent of the VOC emissions from such
products in areas violating the national
ambient air quality standard for ozone.
EPA promulgated this list at 60 FR
15264 (March 23, 1995). EPA plans to
publish a Federal Register notice
announcing that EPA has added
portable gasoline containers to the list of
consumer products to be regulated. This
action must be taken by EPA prior to
issuing a final rule for gas cans. EPA is
required to develop rules reflecting
‘‘best available controls’’ to reduce VOC
emissions from the listed products.
‘‘Best available controls’’ are defined in
section 183(e)(1)(A) as follows:
The term ‘‘best available controls’’ means
the degree of emissions reduction that the
Administrator determines, on the basis of
technological and economic feasibility,
health, environmental, and energy impacts, is
achievable through the application of the
most effective equipment, measures,
processes, methods, systems, or techniques,
including chemical reformulation, product or
feedstock substitution, repackaging, and
directions for use, consumption, storage, or
disposal.’’
Section 183(e)(4) also allows these
standards to be implemented by means
of ‘‘any system or systems of regulation
as the Administrator may deem
appropriate, including requirements for
registration and labeling, selfmonitoring and reporting * * *
concerning the manufacture, processing,
distribution, use, consumption, or
disposal of the product.’’ We are
proposing a hydrocarbon standard for
gas cans under the authority of section
183(e).
c. Energy Policy Act
Section 1504(b) of the Energy Policy
Act of 2005 requires EPA to adjust the
toxics emissions baselines for
reformulated gasoline to reflect 2001–
2002 fuel qualities. However, the Act
provides that this action becomes
unnecessary if EPA takes action which
results in greater overall reductions of
toxics emissions from vehicles in areas
with reformulated gasoline. As
described in section VII of this
preamble, we believe today’s proposed
action would in fact result in greater
reductions than would be achieved by
adjusting the baselines under the Energy
Policy Act. Accordingly, under the
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provisions of the Energy Policy Act, this
proposed action would obviate the need
for readjusting emissions baselines for
reformulated gasoline.
3. What Other Actions Has EPA Taken
Under Clean Air Act Section 202(l)?
a. 2001 Mobile Source Air Toxics Rule
EPA published a final rule under
Clean Air Act section 202(l) on March
29, 2001, entitled, ‘‘Control of Emissions
of Hazardous Air Pollutants from
Mobile Sources’’ (66 FR 17230). This
rule established toxics emissions
performance standards for gasoline
refiners. These standards were designed
to ensure that the over compliance to
the standard seen in the in-use fuels
produced in the years of 1998–2000
would continue in the future.
EPA adopted this anti-backsliding
requirement as a near-term control that
could be implemented and take effect
within a year or two. We did not adopt
long-term controls, those controls that
require a longer lead time to implement,
because we lacked information to
address the costs and benefits of
potential fuel controls in the context of
the fuel sulfur controls that we had
finalized in February 2000. However,
the March 2001 rule did commit to
additional rulemaking that would
evaluate the need for and feasibility of
additional controls.1 Today’s proposal
fulfills that commitment, and represents
the second step of the two-step
approach originally envisioned in the
2001 rule.
The 2001 rule did not set additional
air toxics controls for motor vehicles,
because the technology-forcing Tier 2
light-duty vehicle standards and 2007
heavy-duty engine and vehicle
standards had just been promulgated.
We found that those standards
represented the greatest degree of toxics
control achievable at that time under
section 202(l).2
b. Technical Analysis Plan
The 2001 rulemaking also included a
Technical Analysis Plan that described
toxics-related research and activities
that would inform our future
rulemaking to evaluate the need for and
appropriateness of additional mobile
source air toxic controls. Specifically,
we identified four critical areas where
there were data gaps requiring long-term
efforts:
• Developing better air toxics
emission factors for nonroad sources;
• Improving estimation of air toxics
exposures in microenvironments;
1 See Sierra Club v. EPA, 325 F. 3d 374, 380 (D.C.
Cir. 2003), which upholds this approach.
2 66 FR 17241–17245 (March 29, 2001).
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• Improving consideration of the
range of total public exposures to air
toxics; and
• Increasing our understanding of the
effectiveness and costs of vehicle, fuel
and nonroad controls for air toxics.
EPA and other outside researchers
have conducted significant research in
these areas since 2001. The findings of
this research are described in more
detail in other sections of this preamble
and in the regulatory impact analysis for
this proposal. Following are some
highlights of our activities.
Nonroad emissions testing. EPA has
tested emissions of nonroad diesel
engines for a comprehensive suite of
hydrocarbons and inorganic
compounds. These emissions tests
employed steady-state as well as
transient test cycles, using typical
nonroad diesel fuel and low-sulfur
nonroad diesel fuel. In addition, EPA
tested small gasoline-powered engines
such as lawnmowers, leaf blowers,
chainsaws and string trimmers.
Improved estimation of exposures in
microenvironments and consideration
of the range of public exposures. EPA
and other researchers have conducted a
substantial amount of research and
analysis in these areas, which is
discussed in section IV of this preamble
and in the regulatory impact analysis.
This research has involved monitoring
as well as the development and
application of enhanced modeling tools.
For example, personal exposure
monitoring and ambient monitoring has
been conducted at homes and schools
near roadways; in vehicles; in homes
with attached garages; and in
occupational settings involving both
diesel and gasoline nonroad equipment.
We have also applied dispersion
modeling techniques with greater
spatial refinement to estimate gradients
of toxic pollutants near roadways. A
variety of improvements to our
emissions, dispersion, and exposure
modeling tools are improving our ability
to consider the range of exposure people
experience. These include the MOBILE6
emissions model, improved spatial and
temporal allocation of emissions,
development of the Community
Multiscale Air Quality (CMAQ) model,
and updates to the HAPEM exposure
model. Many of these improvements
were applied in EPA’s National-Scale
Air Toxics Assessment for 1999 and
other analyses EPA performed to
support this proposal. In fact, EPA
developed a modification of the HAPEM
exposure model to account for higher
pollutant concentrations near major
roads.
Research in these areas is continuing
both inside and outside EPA, including
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work under the auspices of the Health
Effects Institute and the Mickey Leland
National Urban Air Toxics Research
Center.
Costs and effectiveness of vehicle,
fuel, and nonroad controls for air toxics.
EPA’s analysis of the costs and
effectiveness of vehicle and fuel
controls is described in section IX of
this preamble and in the regulatory
impact analysis. In addition, as
described in section V, EPA is currently
developing rules that will examine
controls of small gasoline engines and
diesel locomotive and marine engines.
II. Overview of Proposal
A. Why Is EPA Making This Proposal?
People experience elevated risk of
cancer and other noncancer health
effects from exposure to air toxics.
Mobile sources are responsible for a
significant portion of this risk. For
example, benzene is the most significant
contributor to cancer risk from all
outdoor air toxics,3 and most of the
nation’s benzene emissions come from
mobile sources. These risks vary
depending on where people live and
work and the kinds of activities in
which they engage. People who live or
work near major roads, or people that
spend a large amount of time in
vehicles, are likely to have higher
exposures and higher risks. Although
we expect significant reductions in
mobile source air toxics in the future,
predicted cancer and noncancer health
risks will remain a public health
concern. Benzene will remain the
largest contributor to this risk. In
addition, some mobile source air toxics
contribute to the formation of ozone and
PM2.5, which contribute to serious
public health problems, which are
discussed further in section II.A.4.
Sections II.A.1–3 discuss the risks
posed by outdoor toxics now and in the
future, based on national-scale estimates
such as EPA’s National-Scale Air Toxics
Assessment (NATA). EPA’s NATA for
1999 provides some perspective on the
average risk of cancer and noncancer
health effects resulting from breathing
air toxics from outdoor sources, and the
contribution of mobile sources to these
risks.4 5 This assessment did not include
indoor sources of air toxics. Also, it
estimates average concentrations within
3 Based on quantitative estimates of risk, which
do not include diesel particular matter and diesel
exhaust organic gases.
4 https://www.epa.gov/ttn/atw/nata 1999.
5 NATA does not include a quantitative estimate
of cancer risk for diesel particulate matter and
diesel exhaust organic gases. EPA has concluded
that while diesel exhaust is likely to be a human
carcinogen, available data are not sufficient to
develop a confidential estimate of cancer unit risk.
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a census tract, and therefore does not
reflect elevated concentrations and
exposures near roadways within a
census tract. Nevertheless, its findings
are useful in providing a perspective on
the magnitude of risks posed by outdoor
sources of air toxics generally, and in
identifying what pollutants and sources
are important contributors to these
health risks.
EPA also performed a national-scale
assessment for future years, using the
same modeling tools and approach as
the 1999 NATA. Finally, we also
performed national-scale exposure
modeling that accounts for the higher
toxics concentrations near roads. This
latter modeling provides a perspective
on the mobile source contribution to
risk from air toxics that is not reflected
in our other national-scale assessments.
1. National Cancer Risk from Air Toxics
According to NATA, the average
national cancer risk in 1999 from all
outdoor sources of air toxics was 42 in
a million. That is, 42 out of one million
people would be expected to contract
cancer from a lifetime of breathing air
toxics at 1999 levels. Mobile sources
were responsible for 44% of outdoor
toxic emissions and almost 50% of the
cancer risk. Considering only the subset
of compounds emitted by mobile
sources (see Table IV.C–2), the national
average cancer risk in 1999, including
the stationary source contribution to
these pollutants, was 23 in a million.
Benzene is the largest contributor to
cancer risk of all 133 pollutants
quantitatively assessed in the 1999
NATA. The national average cancer risk
from benzene alone was 11 in a million.
Over 120 million people in 1999 were
exposed to a risk level above 10 in a
million due to chronic inhalation
exposure to benzene. Mobile sources
were responsible for 68% of benzene
emissions in 1999.
Although air toxics emissions are
projected to decline in the future as a
result of standards EPA has previously
adopted, cancer risk will continue to be
a public health concern. The predicted
national average cancer risk from
MSATs in 2030 will be 18 in a million,
according to EPA analysis (described in
more detail in section IV of this
preamble and Chapter 3 of the
Regulatory Impact Analysis). In fact, in
2030 there will be more people exposed
to the highest levels of risk. The number
of Americans above the 10 in a million
cancer risk level from exposure to
MSATs is projected to increase from 214
million in 1999 to 240 million in 2030.
Mobile sources will continue to be a
significant contributor to risk in the
future, accounting for 22% of total air
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toxic emissions in 2020, and 44% of
benzene emissions.
2. Noncancer Health Effects
According to the NATA for 1999,
nearly the entire U.S. population was
exposed to an average level of air toxics
that has the potential for adverse
respiratory health effects (noncancer).6
This will continue to be the case in
2030, even though toxics levels will be
lower.
Mobile sources were responsible for
74% of the noncancer (respiratory) risk
from outdoor air toxics in 1999. The
majority of this risk was from acrolein,
and formaldehyde also contributed to
the risk of respiratory health effects.
Mobile sources will continue to be
responsible for the majority of
noncancer risk from outdoor air toxics
in 2030.
Although not included in NATA’s
estimates of noncancer risk, PM from
gasoline and diesel mobile sources
contribute significantly to the health
effects associated with ambient PM, for
which EPA has established a National
Ambient Air Quality Standard. There is
extensive human data showing a wide
spectrum of adverse health effects
associated with exposure to ambient
PM.
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3. Exposure Near Roads and From
Attached Garages
The national-scale risks described
above do not account for higher
exposures experienced by people who
live near major roadways, or people
who live in homes with attached
garages. A substantial number of studies
show elevated concentrations of
multiple MSATs in close proximity to
major roads. We also conducted an
exposure modeling study for three
geographically distinct states (Colorado,
New York, and Georgia) and found that
when the elevated concentrations near
roadways are accounted for, the
distribution of benzene exposure is
broader, with a larger fraction of the
population exposed to higher
concentrations. The largest effect on
personal exposure occurs for the
population living near major roads. A
U.S. Census survey of housing found
that in 2003 12.6% of U.S. housing units
were within 300 feet of a major
transportation source.7 The potential
population exposed to elevated
concentrations near major roadways is
6 That is, the respiratory hazard index exceeded
1. See section III.D of this preamble for more
information.
7 United States Census Bureau. (2004) American
Housing Survey web page. [Online at https://
www.cenus.gov/hhes/www/housing/ahs/ahs03/
ahs03.html] Table IA–6.
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therefore large. In addition, our analysis
indicates that benzene exposure
experienced by people living in homes
with attached garages may be twice the
national average benzene exposure
estimated by NATA for 1999. More
details on exposure near roads and from
attached garages can be found in section
IV of this preamble.
4. Ozone and Particulate Matter
Many MSATs are part of a larger
category of mobile source emissions
known as volatile organic compounds
(VOC), which contribute to the
formation of ozone and particulate
matter (PM). In addition, some MSATs
are emitted directly as PM rather than
being formed through secondary
processes. Thus, MSATs contribute to
adverse health effects both as individual
pollutants, and as precursors to ozone
and PM. Mobile sources contribute
significantly to national emissions of
VOC and PM. In addition, gas cans are
a source of both VOC and benzene
emissions.
Both ozone and PM contribute to
serious public health problems,
including premature mortality,
aggravation of respiratory and
cardiovascular disease (as indicated by
increased hospital admissions and
emergency room visits, school absences,
work loss days, and restricted activity
days), changes in lung function and
increased respiratory symptoms,
changes to lung tissues and structures,
altered respiratory defense mechanisms,
chronic bronchitis, and decreased lung
function.
In addition, ozone and PM cause
significant harm to public welfare.
Specifically, ozone causes damage to
vegetation, which leads to crop and
forestry economic losses, as well as
harm to national parks, wilderness
areas, and other natural systems. PM
contributes to the substantial
impairment of visibility in many parts
of the U.S., including national parks and
wilderness areas. The deposition of
airborne particles can also reduce the
aesthetic appeal of buildings and
culturally important articles through
soiling, and can contribute directly (or
in conjunction with other pollutants) to
structural damage by means of corrosion
or erosion.
Finally, atmospheric deposition and
runoff of polycyclic organic matter
(POM), metals, and other mobile-sourcerelated compounds contribute to the
contamination of water bodies such as
the Great Lakes and coastal waters (e.g.,
the Chesapeake Bay).
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B. What Is EPA Proposing?
1. Light-Duty Vehicle Emission
Standards
As described in more detail in section
VI, we are proposing new standards for
both exhaust and evaporative emissions
from passenger vehicles. The new
exhaust emissions standards would
significantly reduce non-methane
hydrocarbon (NMHC) emissions from
passenger vehicles at cold temperatures.
These hydrocarbons include many
mobile source air toxics (including
benzene), as well as VOC.
Current vehicle emission standards
require that the certification testing of
NMHC is performed at 75 °F. Recent
research and analysis indicates that
these standards are not resulting in
robust control of NMHC at lower
temperatures. We believe that cold
temperature NMHC control can be
substantially improved using the same
technological approaches that are
generally already being used in the Tier
2 vehicle fleet to meet the stringent
standards at 75 °F. These coldtemperature NMHC controls would also
result in lower direct PM emissions at
cold temperatures.
Accordingly, we are proposing that
light-duty vehicles, light-duty trucks,
and medium-duty passenger vehicles
would be subject to a new non-methane
hydrocarbon (NMHC) exhaust emissions
standard at 20 °F. Vehicles at or below
6,000 pounds gross vehicle weight
rating (GVWR) would be subject to a
sales-weighted fleet average NMHC
level of 0.3 grams/mile. Vehicles
between 6,000 and 8,500 pounds GVWR
and medium-duty passenger vehicles
would be subject to a sales-weighted
fleet average NMHC level of 0.5 grams/
mile. For lighter vehicles, the standard
would phase in between 2010 and 2013.
For heavier vehicles, the new standards
would phase in between 2012 and 2015.
We are also proposing a credit program
and other provisions designed to
provide flexibility to manufacturers,
especially during the phase-in periods.
These provisions are designed to allow
the earliest possible phase-in of
standards and help minimize costs and
ease the transition to new standards.
We are also proposing a set of
nominally more stringent evaporative
emission standards for all light-duty
vehicles, light-duty trucks, and
medium-duty passenger vehicles. The
proposed standards are equivalent to
California’s Low Emission Vehicle II
(LEV II) standards, and they reflect the
evaporative emissions levels that are
already being achieved nationwide. The
standards we are proposing today would
codify the approach that most
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manufacturers are already taking for 50state evaporative systems, and the
standards would thus prevent
backsliding in the future. We are
proposing to implement the evaporative
emission standards in 2009 for lighter
vehicles and in 2010 for the heavier
vehicles.
Section VI provides details on the
proposed exhaust and evaporative
standards and their implementation,
and our rationale for proposing them.
2. Gasoline Fuel Standards
As described in more detail in section
VII, we are proposing to limit the
benzene content of all gasoline, both
reformulated and conventional. We
propose that beginning January 1, 2011,
refiners would meet an average gasoline
benzene content standard of 0.62% by
volume on all their gasoline. We are not
proposing a standard for California,
however, because it is already covered
by a similar state program.
This proposed fuel standard would
result in air toxics emissions reductions
that are greater than required under all
existing gasoline toxics programs. As a
result, EPA is proposing that upon full
implementation in 2011, the regulatory
provisions for the benzene control
program would become the single
regulatory mechanism used to
implement the RFG and Anti-dumping
annual average toxics requirements. The
current RFG and Anti-dumping annual
average provisions thus would be
replaced by the proposed benzene
control program. The MSAT2 benzene
control program would also replace the
MSAT1 requirements. In addition, the
program would satisfy certain fuel
MSAT conditions of the Energy Policy
Act of 2005 and obviate the need to
revise toxics baselines for reformulated
gasoline otherwise required by the
Energy Policy Act. In all of these ways,
we would significantly consolidate and
simplify the existing national fuelrelated MSAT regulatory program.
We also propose that refiners could
generate benzene credits and use or
transfer them as a part of a nationwide
averaging, banking, and trading (ABT)
program. From 2007–2010 refiners
could generate benzene credits by taking
early steps to reduce gasoline benzene
levels. Beginning in 2011 and
continuing indefinitely, refiners could
generate credits by producing gasoline
with benzene levels below the 0.62%
average standard. Refiners could apply
the credits towards company
compliance, ‘‘bank’’ the credits for later
use, or transfer (‘‘trade’’) them to other
refiners nationwide (outside of
California) under the proposed program.
Under this program, refiners could use
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credits to achieve compliance with the
benzene content standard.
This proposed ABT program would
allow us to set a more stringent benzene
standard than would otherwise be
possible, and it would allow
implementation to occur earlier. Under
this proposed benzene content standard
and ABT program, gasoline in all areas
of the country would have lower
benzene levels than they have today.
Overall benzene levels would be 37%
lower. This would reduce benzene
emissions and exposure nationwide.
Finally, we propose hardship
provisions. Refiners approved as ‘‘small
refiners’’ would be eligible for certain
temporary relief provisions. In addition,
any refiner facing extreme unforeseen
circumstances or extreme hardship
circumstances could apply for similar
temporary relief.
Section VII of this preamble provides
a detailed explanation and rationale for
the proposed fuel program and its
implementation. It also discusses and
seeks comment on a variety of
alternatives that we considered.
3. Portable Gasoline Container (Gas Can)
Controls
Portable gasoline containers, or gas
cans, are consumer products used to
refuel a wide variety of gasolinepowered equipment, including lawn
and garden equipment, recreational
equipment, and passenger vehicles that
have run out of gas. As described in
section VIII, we are proposing standards
that would reduce hydrocarbon
emissions from evaporation,
permeation, and spillage. These
standards would significantly reduce
benzene and other toxics, as well as
VOC more generally. VOC is an ozone
precursor.
We propose a performance-based
standard of 0.3 grams per gallon per day
of hydrocarbons, based on the emissions
from the can over a diurnal test cycle.
The standard would apply to gas cans
manufactured on or after January 1,
2009. We also propose test procedures
and a certification and compliance
program, in order to ensure that gas cans
would meet the emission standard over
a range of in-use conditions. The
proposed standards would result in the
use of best available control
technologies, such as durable
permeation barriers, automatically
closing spouts, and cans that are wellsealed.
California implemented an emissions
control program for gas cans in 2001,
and since then, several other states have
adopted the program. Last year,
California adopted a revised program,
which will take effect July 1, 2007. The
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revised California program is very
similar to the program we are proposing.
Although a few aspects of the program
we are proposing are different, we
believe manufacturers would be able to
meet both EPA and California
requirements with the same gas can
designs.
III. What Are Mobile Source Air Toxics
(MSATs) and Their Health Effects?
A. What Are MSATs?
Section 202(l) refers to ‘‘hazardous air
pollutants from motor vehicles and
motor vehicle fuels.’’ We use the term
‘‘mobile source air toxics (MSATs)’’ to
refer to compounds that are emitted by
mobile sources and have the potential
for serious adverse health effects. There
are a variety of ways in which to
identify compounds that have the
potential for serious adverse health
effects. For example, EPA’s Integrated
Risk Information System (IRIS) is EPA’s
database containing information on
human health effects that may result
from exposure to various chemicals in
the environment. In addition, Clean Air
Act section 112(b) contains a list of
hazardous air pollutants that EPA is
required to control through regulatory
standards; other agencies or programs
such as the Agency for Toxic Substances
and Disease Registry and the California
EPA have developed health benchmark
values for various compounds; and the
International Agency for Research on
Cancer and the National Toxicology
Program have assembled evidence of
substances that cause cancer in humans
and issue judgments on the strength of
the evidence. Each source of
information has its own strengths and
limitations. For example, there are
inherent limitations on the number of
compounds that have been investigated
sufficiently for EPA to conduct an IRIS
assessment. There are some compounds
that are not listed in IRIS but are
considered to be hazardous air
pollutants under Clean Air Act section
112(b) and are regulated by the Agency
(e.g., propionaldehyde, 2,2,4trimethylpentane).
B. Compounds Emitted by Mobile
Sources and Identified in IRIS
In its 2001 MSAT rule, EPA identified
a list of 21 MSATs. We listed a
compound as an MSAT if it was emitted
from mobile sources, and if the Agency
had concluded in IRIS that the
compound posed a potential cancer
hazard and/or if IRIS contained an
inhalation reference concentration or
ingestion reference dose for the
compound. Since 2001, EPA has
conducted an extensive review of the
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literature to produce a list of the
compounds identified in the exhaust or
evaporative emissions from onroad and
nonroad equipment, using baseline as
well as alternative fuels (e.g., biodiesel,
compressed natural gas). This list, the
Master List of Compounds Emitted by
Mobile Sources (‘‘Master List’’),
currently includes approximately 1,000
compounds. It is available in the public
docket for this rule and on the web
(www.epa.gov/otaq/toxics.htm). Table
III.B–1 lists those compounds from the
Master List that currently meet those
2001 MSAT criteria, based on the
current IRIS.
Table III.B–1 identifies all of the
compounds from the Master List that are
present in IRIS with (a) a cancer hazard
identification of known, probable, or
possible human carcinogens (under the
1986 EPA cancer guidelines) or
carcinogenic to humans, likely to be
carcinogenic to humans, or suggestive
evidence of carcinogenic potential
(under the 2005 EPA cancer guidelines);
and/or (b) an inhalation reference
concentration or an ingestion reference
dose. Although all these compounds
have been detected in emissions from
mobile sources, many are emitted in
trace amounts and data are not adequate
to develop an inventory. Those
compounds for which we have
developed an emissions inventory are
summarized in Table IV.C–2. There are
several compounds for which IRIS
assessments are underway and therefore
15813
are not included in Table III.B–1. These
compounds are: Cerium, copper,
ethanol, ethyl tertiary butyl ether
(ETBE), platinum, propionaldehyde,
and 2,2,4-trimethylpentane.
The fact that a compound is listed in
Table III.B–1 does not imply a risk to
public health or welfare at current
levels, or that it is appropriate to adopt
controls to limit the emissions of such
a compound from motor vehicles or
their fuels. In conducting any such
further evaluation, pursuant to sections
202(a) or 211(c) of the Act, EPA would
consider whether emissions of the
compound from motor vehicles cause or
contribute to air pollution which may
reasonably be anticipated to endanger
public health or welfare.
TABLE III.B–1.—COMPOUNDS EMITTED BY MOBILE SOURCES THAT ARE LISTED IN IRIS*
1,1,1,2-Tetrafluoroethane ...................................
1,1,1-Trichloroethane .........................................
1,1-Biphenyl ........................................................
1,2-Dibromoethane .............................................
1,2-Dichlorobenzene ..........................................
1,3-Butadiene .....................................................
2,4-Dinitrophenol ................................................
2-Methylnaphthalene ..........................................
2-Methylphenol ...................................................
4-Methylphenol ...................................................
Acenaphthene ....................................................
Acetaldehyde ......................................................
Acetone ..............................................................
Acetophenone ....................................................
Acrolein (2-propenal) ..........................................
Ammonia ............................................................
Anthracene .........................................................
Antimony .............................................................
Arsenic, inorganic ...............................................
Barium and compounds .....................................
Benz[a]anthracene .............................................
Benzaldehyde .....................................................
Benzene .............................................................
Benzo[a]pyrene (BaP) ........................................
Benzo[b]fluoranthene .........................................
Benzo[k]fluoranthene ..........................................
Benzoic acid .......................................................
Beryllium and compounds ..................................
Boron (Boron and Borates only) ........................
Bromomethane ...................................................
Butyl benzyl phthalate ........................................
Cadmium ..........................................................
Carbon disulfide ...............................................
Carbon tetrachloride ........................................
Chlorine ............................................................
Chlorobenzene .................................................
Chloroform .......................................................
Chromium III ....................................................
Chromium VI ....................................................
Chrysene ..........................................................
Crotonaldehyde ................................................
Cumene (isopropyl benzene) ...........................
Cyclohexane ....................................................
Cyclohexanone ................................................
Di(2-ethylhexyl)phthalate .................................
Dibenz[a,h]anthracene .....................................
Dibutyl phthalate ..............................................
Dichloromethane ..............................................
Diesel PM and Diesel exhaust organic gases
Diethyl phthalate ..............................................
Ethylbenzene ...................................................
Ethylene glycol monobutyl ether ......................
Fluoranthene ....................................................
Fluorene ...........................................................
Formaldehyde ..................................................
Furfural .............................................................
Hexachlorodibenzo-p-dioxin, mixture (dioxin/
furans).
n-Hexane ..........................................................
Hydrogen cyanide ............................................
Hydrogen sulfide ..............................................
Indeno[1,2,3-cd]pyrene ....................................
Lead and compounds (inorganic) ....................
Manganese.
Mercury, elemental.
Methanol.
Methyl chloride.
Methyl ethyl ketone (MEK).
Methyl isobutyl ketone (MIBK).
Methyl tert-butyl ether (MTBE).
Molybdenum.
Naphthalene.
Nickel.
Nitrate.
N-Nitrosodiethylamine.
N-Nitrosodimethylamine.
N-Nitroso-di-n-butylamine.
N-Nitrosodi-N-propylamine.
N-Nitrosopyrrolidine.
Pentachlorophenol.
Phenol.
Phosphorus.
Phthalic anhydride.
Pyrene.
Selenium and compounds.
Silver.
Strontium.
Styrene.
Tetrachloroethylene.
Toluene.
Trichlorofluoromethane.
Vanadium.
Xylenes.
Zinc and compounds.
* Compounds listed in IRIS as known, probable, or possible human carcinogens and/or pollutants for which the Agency has calculated a reference concentration or reference dose.
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C. Which Mobile Source Emissions Pose
the Greatest Health Risk at Current
Levels?
The 1999 National-Scale Air Toxics
Assessment (NATA) provides some
perspective on which mobile source
emissions pose the greatest risk at
current estimated ambient levels.8 We
also conducted a national-scale
assessment for future years, which is
discussed more fully in section IV of
this preamble and Chapters 2 and 3 of
the RIA. Our understanding of what
emissions pose the greatest risk will
evolve over time, based on our
understanding of the ambient levels and
8 It is, of course, not necessary for EPA to show
that a compound is a national or regional risk driver
to show that its emission from motor vehicles may
reasonably cause or contribute to endangerment of
public health or welfare. A showing that motor
vehicles contribute some non-trivial percentage of
the inventory of a compound known to be
associated with adverse health effects would
normally be sufficient. Cf. Bluewater Network v.
EPA, 370 F. 3d 1, 15 (D.C. Cir. 2004).
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health effects associated with the
compounds.9
1. National and Regional Risk Drivers in
1999 National-Scale Air Toxics
Assessment
The 1999 NATA evaluates 177
hazardous air pollutants currently listed
under CAA section 112(b), as well as
9 The discussion here considers risks other than
those attributed to ambient levels of criteria
pollutants.
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Federal Register / Vol. 71, No. 60 / Wednesday, March 29, 2006 / Proposed Rules
diesel PM.10 NATA is described in
greater detail in Chapters 2 and 3 of the
Regulatory Impact Analysis for this
proposed rule. Additional information
can also be obtained from the NATA
website (https://www.epa.gov/ttn/atw/
nata1999). Based on the assessment of
inhalation exposures associated with
outdoor sources of these hazardous air
pollutants, NATA has identified cancer
and noncancer risk drivers on a national
and regional scale (Table III.C–1). A
cancer risk driver on a national scale is
a hazardous air pollutant for which at
least 25 million people are exposed to
risk greater than ten in one million.
Benzene is the only compound
identified in the 1999 NATA as a
national cancer risk driver. A cancer
risk driver on a regional scale is a
hazardous air pollutant for which at
least one million people are exposed to
risk greater than ten in one million or
at least 10,000 people are exposed to
risk greater than 100 in one million.
Twelve compounds (or groups of
compounds in the case of POM) were
identified as regional cancer risk
drivers. The 1999 NATA concludes that
diesel particulate matter is among the
substances that pose the greatest relative
risk, although the cancer risk cannot be
quantified.
A noncancer risk driver at the
national scale is a hazardous air
pollutant for which at least 25 million
people are exposed at a concentration
greater than the inhalation reference
concentration. The RfC is an estimate
(with uncertainty spanning perhaps an
order of magnitude) of a daily exposure
to the human population (including
sensitive subgroups) that is likely to be
without appreciable risk of deleterious
effects during a lifetime. Acrolein is the
only compound identified in the 1999
NATA as a national noncancer risk
driver. A noncancer risk driver on a
regional scale is defined as a hazardous
air pollutant for which at least 10,000
people are exposed to an ambient
concentration greater than the
inhalation reference concentration.
Sixteen regional-scale noncancer risk
drivers were identified in the 1999
NATA (see Table III.C–1.).
TABLE III.C–1.—NATIONAL AND REGIONAL CANCER AND NONCANCER
RISK DRIVERS IN 1999 NATA
Cancer 1
Noncancer
National drivers 2 .......
Benzene ....................
Regional drivers 3 ......
Arsenic compounds ..
Benzidine ..................
1,3-Butadiene ............
Cadmium compounds
Carbon tetrachloride
Chromium VI .............
Coke oven .................
Ethylene oxide ..........
Hydrazine ..................
National drivers 4
Acrolein
Regional drivers 5
Antimony
Arsenic compounds
1,3-Butadiene
Cadmium compounds
Chlorine
Chromium VI
Diesel PM
Formaldehyde
Hexamethylene 1–6diisocyanate
Hydrazine
Hydrochloric acid
Maleic anhydride
Naphthalene ..............
Perchloroethylene .....
Polycyclic organic
matter.
Manganese compounds
TABLE III.C–1.—NATIONAL AND REGIONAL CANCER AND NONCANCER
RISK DRIVERS IN 1999 NATA—
Continued
Cancer 1
Noncancer
Nickel compounds
2,4-Toluene
diisocyanate
Triethylamine
1 The list of cancer risk drivers does not include diesel particulate matter. However, the
1999 NATA concluded that it was one of the
pollutants that posed the greatest relative cancer risk.
2 At least 25 million people exposed to risk
>10 in 1 million.
3 At least 1 million people exposed to risk
>10 in 1 million or at least 10,000 people exposed to risk >100 in 1 million.
4 At least 25 million people exposed to a
hazard quotient > 1.0.
5 At least 10,000 people exposed to a hazard quotient > 1.
2. 1999 NATA Risk Drivers with
Significant Mobile Source Contribution
Among the national and regionalscale cancer and noncancer risk drivers
identified in the 1999 NATA, seven
compounds have significant
contributions from mobile sources:
benzene, 1,3-butadiene, formaldehyde,
acrolein, polycyclic organic matter
(POM), naphthalene, and diesel
particulate matter and diesel exhaust
organic gases (Table III.C–2.). For
example, mobile sources contribute
68% of the national benzene inventory,
with 49% from on-road sources and
19% from nonroad sources.
TABLE III.C–2.—MOBILE SOURCE CONTRIBUTION TO 1999 NATA RISK DRIVERS
Percent contribution from
all mobile
sources
(percent)
1999 NATA risk drivers
Benzene ...................................................................................................................................................................
1,3–Butadiene ..........................................................................................................................................................
Formaldehyde ..........................................................................................................................................................
Acrolein ....................................................................................................................................................................
Polycyclic organic matter * .......................................................................................................................................
Naphthalene .............................................................................................................................................................
Diesel PM and Diesel exhaust organic gases ........................................................................................................
68
58
47
25
6
27
100
Percent contribution from
on-road mobile
sources
(percent)
49
41
27
14
3
21
38
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* This POM inventory includes the 15 POM compounds: benzo[b]fluoranthene, benz[a]anthracene, indeno(1,2,3-c,d)pyrene,
benzo[k]fluoranthene, chrysene, benzo[a]pyrene, dibenz(a,h)anthracene, anthracene, pyrene, benzo(g,h,i)perylene, fluoranthene, acenaphthylene,
phenanthrene, fluorene, and acenaphthene.
10 NATA does not include a quantitative estimate
of cancer risk for diesel particulate matter and
diesel exhaust organic gases.
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D. What Are the Health Effects of Air
Toxics?
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1. Overview of Potential Cancer and
Noncancer Health Effects
Air toxics can cause a variety of
cancer and noncancer health effects. A
number of the mobile source air toxic
pollutants described in section III are
known or likely to pose a cancer hazard
in humans. Many of these compounds
also cause adverse noncancer health
effects resulting from chronic,11
subchronic,12 or acute 13 inhalation
exposures. These include neurological,
cardiovascular, liver, kidney, and
respiratory effects as well as effects on
the immune and reproductive systems.
Section III.D.2 discusses the health
effects of air toxic compounds listed in
Table III.C–2, as well as acetaldehyde.
The compounds in Table III.C–2 were
all identified as national and regionalscale cancer and noncancer risk drivers
in the 1999 National-Scale Air Toxics
Assessment (NATA), and have
significant inventory contributions from
mobile sources. Acetaldehyde is
included because it is a likely human
carcinogen, has a significant inventory
contribution from mobile sources, and
was identified as a risk driver in the
1996 NATA. We are also including
diesel particulate matter and diesel
exhaust organic gases in this discussion.
Although 1999 NATA did not quantify
cancer risks associated with exposure to
this pollutant, EPA has concluded that
diesel exhaust ranks with the other
substances that the national-scale
assessment suggests pose the greatest
relative risk.14
Inhalation cancer risks are usually
estimated by EPA as ‘‘unit risks,’’ which
represent the excess lifetime cancer risk
estimated to result from continuous
exposure to an agent at a concentration
of 1 µg/m3 in air. Some air toxics are
known to be carcinogenic in animals but
lack data in humans. These have been
assumed to be human carcinogens. Also,
relationships between exposure and
probability of cancer are assumed to be
linear. In addition, these unit risks are
typically upper bound estimates. Upper
bound estimates are more likely to
11 Chronic exposure is defined in the glossary of
the Integrated Risk Information (IRIS) database
(www.epa.gov/iris) as repeated exposure by the oral,
dermal, or inhalation route for more than
approximately 10 of the life span in humans (more
than approximately 90 days to 2 years in typically
used laboratory animal species).
12 Defined in the IRIS database as exposure to a
substance spanning approximately 10 of the
lifetime of an organism.
13 Defined in the IRIS database as exposure by the
oral, dermal, or inhalation route for 24 hours or
less.
14 https://www.epa.gov/ttn/atw/nata1999.
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overestimate than underestimate risk.
Where there are strong epidemiological
data, a maximum likelihood (MLE)
estimate may be developed. An MLE is
a best scientific estimate of risk. The
benzene unit risk is an MLE. A
discussion of the confidence in a
quantitative cancer risk estimate is
provided in the IRIS file for each
compound. The discussion of the
confidence in the cancer risk estimate
includes an assessment of the source of
the data (human or animal),
uncertainties in dose estimates, choice
of the model used to fit the exposure
and response data and how
uncertainties and potential confounders
are handled.
Potential noncancer chronic
inhalation health risks are quantified
using reference concentrations (RfCs)
and noncancer chronic ingestion health
risks are quantified using reference
doses (RfDs). The RfC is an estimate
(with uncertainty spanning perhaps an
order of magnitude) of a daily exposure
to the human population (including
sensitive subgroups) that is likely to be
without appreciable risk of deleterious
effects during a lifetime. Sources of
uncertainty in the development of the
RfCs and RfDs include intraspecies
extrapolation (animal to human) and
interspecies extrapolation (average
human to sensitive human). Additional
sources of uncertainty can be using a
lowest observed adverse effect level in
place of a no observed adverse effect
level, and other data deficiencies. A
statement regarding the confidence in
the RfC and/or RfD is developed to
reflect the confidence in the principal
study or studies on which the RfC or
RfD are based and the confidence in the
underlying database. Factors that affect
the confidence in the principal study
include how well the study was
designed, conducted and reported.
Factors that affect the confidence in the
database include an assessment of the
availability of information regarding
identification of the critical effect,
potentially susceptible populations and
exposure scenarios relevant to
assessment of risk.
The RfC may be used to estimate a
hazard quotient, which is the
environmental exposure to a substance
divided by its RfC. A hazard quotient
greater than one indicates adverse
health effects are possible. The hazard
quotient cannot be translated to a
probability that adverse health effects
will occur, and is unlikely to be
proportional to risk. It is especially
important to note that a hazard quotient
exceeding one does not necessarily
mean that adverse effects will occur. In
NATA, hazard quotients for different
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15815
respiratory irritants were also combined
into a hazard index (HI). A hazard index
is the sum of hazard quotients for
substances that affect the same target
organ or organ system. Because different
pollutants may cause similar adverse
health effects, it is often appropriate to
combine hazard quotients associated
with different substances. However, the
HI is only an approximation of a
combined effect because substances may
affect a target organ in different ways.
2. Health Effects of Key MSATs
a. Benzene
The EPA’s IRIS database lists
benzene, an aromatic hydrocarbon, as a
known human carcinogen (causing
leukemia) by all routes of exposure.15 A
number of adverse noncancer health
effects including blood disorders and
immunotoxicity have also been
associated with long-term occupational
exposure to benzene.
Inhalation is the major source of
human exposure to benzene in the
occupational and non-occupational
setting. Long-term inhalation
occupational exposure to benzene has
been shown to cause cancer of the
hematopoetic (blood cell) system in
adults. Among these are acute
nonlymphocytic leukemia 16 and
chronic lymphocytic leukemia.17 18
15 U.S. EPA (2000). Integrated Risk Information
System File for Benzene. This material is available
electronically at https://www.epa.gov/iris/subst/
0276.htm.
16 Leukemia is a blood disease in which the white
blood cells are abnormal in type or number.
Leukemia may be divided into nonlymphocytic
(granulocytic) leukemias and lymphocytic
leukemias. Nonlymphocytic leukemia generally
involves the types of white blood cells (leukocytes)
that are involved in engulfing, killing, and digesting
bacteria and other parasites (phagocytosis) as well
as releasing chemicals involved in allergic and
immune responses. This type of leukemia may also
involve erythroblastic cell types (immature red
blood cells). Lymphocytic leukemia involves the
lymphocyte type of white blood cells that are
responsible for the immune responses. Both
nonlymphocytic and lymphocytic leukemia may, in
turn, be separated into acute (rapid and fatal) and
chronic (lingering, lasting) forms. For example; in
acute myeloid leukemia there is diminished
production of normal red blood cells (erythrocytes),
granulocytes, and platelets (control clotting), which
leads to death by anemia, infection, or hemorrhage.
These events can be rapid. In chronic myeloid
leukemia (CML) the leukemic cells retain the ability
to differentiate (i.e., be responsive to stimulatory
factors) and perform function; later there is a loss
of the ability to respond.
17 U.S. EPA (1985) Environmental Protection
Agency, Interim quantitative cancer unit risk
estimates due to inhalation of benzene, prepared by
the Office of Health and Environmental
Assessment, Carcinogen Assessment Group,
Washington, DC, for the Office of Air Quality
Planning and Standards, Washington, DC, 1985.
18 U.S. EPA. (1993). Motor Vehicle-Related Air
Toxics Study. Office of Mobile Sources, Ann Arbor,
MI. https://www.epa.gov/otaq/regs/toxics/
tox_archive.htm.
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Leukemias, lymphomas, and other
tumor types have been observed in
experimental animals exposed to
benzene by inhalation or oral
administration. Exposure to benzene
and/or its metabolites has also been
linked with chromosomal changes in
humans and animals 19 20 and increased
proliferation of mouse bone marrow
cells.21 22
The latest assessment by EPA places
the excess risk of developing acute
nonlymphocytic leukemia from
inhalation exposure to benzene at 2.2 ×
10¥6 to 7.8 × 10¥6 per µg/m3. In other
words, there is a risk of about two to
eight excess leukemia cases in one
million people exposed to 1 µg/m3 of
benzene over a lifetime.23 This range of
unit risks are the MLEs calculated from
different exposure assumptions and
dose-response models that are linear at
low doses. At present, the true cancer
risk from exposure to benzene cannot be
ascertained, even though dose-response
data are used in the quantitative cancer
risk analysis, because of uncertainties in
the low-dose exposure scenarios and
lack of clear understanding of the mode
of action. A range of estimates of risk is
recommended, each having equal
scientific plausibility. There are
confidence intervals associated with the
MLE range that reflect random variation
of the observed data. For the upper end
of the MLE range, the 5th and 95th
percentile values are about a factor of 5
lower and higher than the best fit value.
The upper end of the MLE range was
used in NATA.
It should be noted that not enough
information is known to determine the
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19 International
Agency for Research on Cancer
(IARC) (1982) IARC monographs on the evaluation
of carcinogenic risk of chemicals to humans,
Volume 29, Some industrial chemicals and
dyestuffs, International Agency for Research on
Cancer, World Health Organization, Lyon, France,
p. 345–389.
20 U.S. EPA (1998) Environmental Protection
Agency, Carcinogenic Effects of Benzene: An
Update, National Center for Environmental
Assessment, Washington, DC. EPA600–P–97–001F.
https://www.epa.gov/ncepihom/Catalog/
EPA600P97001F.html.
21 Irons, R.D., W.S. Stillman, D.B. Colagiovanni,
and V.A. Henry (1992) Synergistic action of the
benzene metabolite hydroquinone on myelopoietic
stimulating activity of granulocyte/macrophage
colony-stimulating factor in vitro, Proc. Natl. Acad.
Sci. 89:3691–3695.
22 U.S. EPA (1998) Environmental Protection
Agency, Carcinogenic Effects of Benzene: An
Update, National Center for Environmental
Assessment, Washington, DC. EPA600–P–97–001F.
https://www.epa.gov/ncepihom/Catalog/
EPA600P97001F.html.
23 U.S. EPA (1998). Environmental Protection
Agency, Carcinogenic Effects of Benzene: An
Update, National Center for Environmental
Assessment, Washington, DC. EPA600–P–97–001F.
https://www.epa.gov/ncepihom/Catalog/
EPA600P97001F.html.
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slope of the dose-response curve at
environmental levels of exposure and to
provide a sound scientific basis to
choose any particular extrapolation/
exposure model to estimate human
cancer risk at low doses. EPA risk
assessment guidelines suggest using an
assumption of linearity of dose response
when (1) there is an absence of
sufficient information on modes of
action or (2) the mode of action
information indicates that the doseresponse curve at low dose is or is
expected to be linear.24 Since the mode
of action for benzene carcinogenicity is
unknown, the current cancer unit risk
estimate assumes linearity of the lowdose response. Data that were
considered by EPA in its carcinogenic
update suggested that the dose-response
relationship at doses below those
examined in the studies reviewed in
EPA’s most recent benzene assessment
may be supralinear. They support the
inference that cancer risks are as high or
are higher than the estimates provided
in the existing EPA assessment.25 Data
discussed in the EPA IRIS assessment
suggest that genetic abnormalities occur
at low exposure in humans, and the
formation of toxic metabolites plateaus
above 25 ppm (80,000 µg/m3).26 More
recent data on benzene adducts in
humans, published after the most recent
IRIS assessment, suggest that the
enzymes involved in benzene
metabolism start to saturate at exposure
levels as low as 1 ppm.27 Because there
is a transition from linear to saturable
metabolism below 1 ppm, the
assumption of low-dose linearity
extrapolated from much higher
exposures could lead to substantial
underestimation of leukemia risks. This
is consistent with recent
epidemiological data which also suggest
a supralinear exposure-response
relationship and which ‘‘[extend]
evidence for hematopoietic cancer risks
to levels substantially lower than had
previously been established.’’ 28 29 These
24 U.S. EPA (2005) Guidelines for Carcinogen Risk
Assessment. Report No. EPA/630/P–03/001F.
https://cfpub.epa.gov/ncea/raf/
recordisplay.cfm?deid=116283.
25 U.S. EPA (1998) Carcinogenic Effects of
Benzene: An Update. EPA/600/P–97/001F.
26 Rothman, N; Li, GL; Dosemeci, M; et al. (1996)
Hematotoxicity among Chinese workers heavily
exposed to benzene. Am. J. Indust. Med. 29:236–
246.
27 Rappaport, S.M.; Waidyanatha, S.; Qu, Q.;
Shore, R.; Jin, X.; Cohen, B.; Chen, L.; Melikian, A.;
Li, G.; Yin, S.; Yan, H.; Xu, B.; Mu, R.; Li, Y.; Zhang,
X.; and Li, K. (2002) Albumin adducts of benzene
oxide and 1,4-benzoquinone as measures of human
benzene metabolism. Cancer Research 62:1330–
1337.
28 Hayes, R.B.; Yin, S.; Dosemeci, M.; Li, G.;
Wacholder, S.; Travis, L.B.; Li, C.; Rothman, N.;
Hoover, R.N.; and Linet, M.S. (1997) Benzene and
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data are from the largest cohort study
done to date with individual worker
exposure estimates. However, these data
have not yet been formally evaluated by
EPA as part of the IRIS review process,
and it is not clear whether these data
provide sufficient evidence to reject a
linear dose-response curve. A better
understanding of the biological
mechanism of benzene-induced
leukemia is needed.
Children may represent a
subpopulation at increased risk from
benzene exposure, due to factors that
could increase their susceptibility.
Children may have a higher unit body
weight exposure because of their
heightened activity patterns which can
increase their exposures, as well as
different ventilation tidal volumes and
frequencies, factors that influence
uptake. This could entail a greater risk
of leukemia and other toxic effects to
children if they are exposed to benzene
at similar levels as adults. There is
limited information from two studies
regarding an increased risk to children
whose parents have been occupationally
exposed to benzene.30 31 Data from
animal studies have shown benzene
exposures result in damage to the
hematopoietic (blood cell formation)
system during development.32 33 34 Also,
key changes related to the development
of childhood leukemia occur in the
developing fetus.35 Several studies have
reported that genetic changes related to
eventual leukemia development occur
before birth. For example, there is one
study of genetic changes in twins who
developed T cell leukemia at 9 years of
the dose-related incidence of hematologic
neoplasms in China. J. Nat. Cancer Inst. 89:1065–
1071.
29 Hayes, R.B.; Songnian, Y.; Dosemeci, M.; and
Linet, M. (2001) Benzene and lymphohematopoietic
malignancies in humans. Am. J. Indust. Med.
40:117–126.
30 Shu, X.O,; Gao, Y.T.; Brinton, L.A.; et al. (1988)
A population-based case-control study of childhood
leukemia in Shanghai. Cancer 62:635–644.
31 McKinney, P.A.; Alexander, F.E.; Cartwright,
R.A.; et al. (1991) Parental occupations of children
with leukemia in west Cumbria, north Humberside,
and Gateshead, Br. Med. J. 302:681–686.
32 Keller, KA; Snyder, CA. (1986) Mice exposed
in utero to low concentrations of benzene exhibit
enduring changes in their colony forming
hematopoietic cells. Toxicology 42:171–181.
33 Keller, KA; Snyder, CA. (1988) Mice exposed
in utero to 20 ppm benzene exhibit altered numbers
of recognizable hematopoietic cells up to seven
weeks after exposure. Fundam. Appl. Toxicol.
10:224–232.
34 Corti, M; Snyder, CA. (1996) Influences of
gender, development, pregnancy and ethanol
consumption on the hematotoxicity of inhaled 10
ppm benzene. Arch. Toxicol. 70:209–217.
35 U.S. EPA. (2002). Toxicological Review of
Benzene (Noncancer Effects). National Center for
Environmental Assessment, Washington, DC.
Report No. EPA/635/R–02/001F. https://
www.epa.gov/iris/toxreviews/0276-tr[1].pdf.
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age.36 An association between traffic
volume, residential proximity to busy
roads and occurrence of childhood
leukemia has also been identified in
some studies, although some studies
show no association.
A number of adverse noncancer
health effects, including blood disorders
such as preleukemia and aplastic
anemia, have also been associated with
long-term exposure to benzene.37 38
People with long-term occupational
exposure to benzene have experienced
harmful effects on the blood-forming
tissues, especially in bone marrow.
These effects can disrupt normal blood
production and suppress the production
of important blood components, such as
red and white blood cells and blood
platelets, leading to anemia (a reduction
in the number of red blood cells),
leukopenia (a reduction in the number
of white blood cells), or
thrombocytopenia (a reduction in the
number of blood platelets, thus reducing
the ability of blood to clot). Chronic
inhalation exposure to benzene in
humans and animals results in
pancytopenia,39 a condition
characterized by decreased numbers of
circulating erythrocytes (red blood
cells), leukocytes (white blood cells),
and thrombocytes (blood platelets).40 41
Individuals that develop pancytopenia
and have continued exposure to
benzene may develop aplastic anemia,
whereas others exhibit both
pancytopenia and bone marrow
hyperplasia (excessive cell formation), a
condition that may indicate a
36 Ford, AM; Pombo-de-Oliveira, MS; McCarthy,
KP; MacLean, JM; Carrico, KC; Vincent, RF;
Greaves, M. (1997) Monoclonal origin of concordant
T-cell malignancy in identical twins. Blood 89:281–
285.
37 Aksoy, M. (1989) Hematotoxicity and
carcinogenicity of benzene. Environ. Health
Perspect. 82:193–197.
38 Goldstein, B.D. (1988) Benzene toxicity.
Occupational medicine. State of the Art Reviews 3:
541–554.
39 Pancytopenia is the reduction in the number of
all three major types of blood cells (erythrocytes, or
red blood cells, thrombocytes, or platelets, and
leukocytes, or white blood cells). In adults, all three
major types of blood cells are produced in the bone
marrow of the vertebra, sternum, ribs, and pelvis.
The bone marrow contains immature cells, known
as multipotent myeloid stem cells, that later
differentiate into the various mature blood cells.
Pancytopenia results from a reduction in the ability
of the red bone marrow to produce adequate
numbers of these mature blood cells.
40 Aksoy, M. (1991) Hematotoxicity,
leukemogenicity and carcinogenicity of chronic
exposure to benzene. In: Arinc, E.; Schenkman, J.B.;
Hodgson, E., Eds. Molecular Aspects of
Monooxygenases and Bioactivation of Toxic
Compounds. New York: Plenum Press, pp. 415–434.
41 Goldstein, B.D. (1988) Benzene toxicity.
Occupational medicine. State of the Art Reviews 3:
541–554.
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preleukemic state.42 43 The most
sensitive noncancer effect observed in
humans, based on current data, is the
depression of the absolute lymphocyte
count in blood.44 45
EPA’s inhalation reference
concentration (RfC) for benzene is 30
µg/m3, based on suppressed absolute
lymphocyte counts as seen in humans
under occupational exposure
conditions. The overall confidence in
this RfC is medium. Since development
of this RfC, there have appeared human
reports of benzene’s hematotoxic effects
in the literature that provides data
suggesting a wide range of
hematological endpoints that are
affected at occupational exposures of
less than 5 ppm (about 16 mg/m3) 46 and
even at air levels of 1 ppm (about 3 mg/
m3) or less among genetically
susceptible populations.47 One recent
study found benzene metabolites in
mouse liver and bone marrow at
environmental doses, indicating that
even concentrations in urban air can
elicit a biochemical response in rodents
that indicates toxicity.48 EPA has not
formally evaluated these recent studies
as part of the IRIS review process to
determine whether or not they will lead
to a change in the current RfC. EPA does
not currently have an acute reference
concentration for benzene. The Agency
for Toxic Substances and Disease
Registry Minimal Risk Level for acute
exposure to benzene is 160 µg/m3 for 1–
14 days exposure.
b. 1,3-Butadiene
EPA has characterized 1,3-butadiene,
a hydrocarbon, as a leukemogen,
42 Aksoy, M., S. Erdem, and G. Dincol. (1974)
Leukemia in shoe-workers exposed chronically to
benzene. Blood 44:837.
43 Aksoy, M. and K. Erdem. (1978) A follow-up
study on the mortality and the development of
leukemia in 44 pancytopenic patients associated
with long-term exposure to benzene. Blood 52: 285–
292.
44 Rothman, N., G.L. Li, M. Dosemeci, W.E.
Bechtold, G.E. Marti, Y.Z. Wang, M. Linet, L.Q. Xi,
W. Lu, M.T. Smith, N. Titenko-Holland, L.P. Zhang,
W. Blot, S.N. Yin, and R.B. Hayes (1996)
Hematotoxicity among Chinese workers heavily
exposed to benzene. Am. J. Ind. Med. 29: 236–246.
45 EPA 2005 ‘‘Full IRIS Summary for Benzene
(CASRN 71–43–2)’’ Environmental Protection
Agency, Integrated Risk Information System (IRIS),
Office of Health and Environmental Assessment,
Environmental Criteria and Assessment Office,
Cincinnati, OH https://www.epa.gov/iris/subst/
0276.htm.
46 Qu, Q., R. Shore, G. Li, X. Jin, L.C. Chen, B.
Cohen, et al. (2002). Hematological changes among
Chinese workers with a broad range of benzene
exposures. Am. J. Industr. Med. 42: 275–285.
47 Lan, Qing, Zhang, L., Li, G., Vermeulen, R., et
al. (2004). Hematotoxically in Workers Exposed to
Low Levels of Benzene. Science 306: 1774–1776.
48 Turtletaub, K.W. and Mani, C. (2003). Benzene
metabolism in rodents at doses relevant to human
exposure from Urban Air. Res Rep Health Effect Inst
113.
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carcinogenic to humans by
inhalation.49 50 The specific mechanisms
of 1,3-butadiene-induced carcinogenesis
are unknown; however, it is virtually
certain that the carcinogenic effects are
mediated by genotoxic metabolites of
1,3-butadiene. Animal data suggest that
females may be more sensitive than
males for cancer effects; nevertheless,
there are insufficient data from which to
draw any conclusions on potentially
sensitive subpopulations. The upper
bound cancer unit risk estimate is 0.08
per ppm or 3×10¥5 per µg/m3 (based
primarily on linear modeling and
extrapolation of human data). In other
words, it is estimated that
approximately 30 persons in one
million exposed to 1 µg/m3 of 1,3butadiene continuously for their
lifetime would develop cancer as a
result of this exposure. The human
incremental lifetime unit cancer risk
estimate is based on extrapolation from
leukemias observed in an occupational
epidemiologic study.51 This estimate
includes a two-fold adjustment to the
epidemiologic-based unit cancer risk
applied to reflect evidence from the
rodent bioassays suggesting that the
epidemiologic-based estimate (from
males) may underestimate total cancer
risk from 1,3-butadiene exposure in the
general population, particularly for
breast cancer in females. Confidence in
the excess cancer risk estimate of 0.08
per ppm is moderate.
1,3-Butadiene also causes a variety of
reproductive and developmental effects
in mice; no human data on these effects
are available. The most sensitive effect
was ovarian atrophy observed in a
lifetime bioassay of female mice.52
Based on this critical effect and the
benchmark concentration methodology,
an RfC was calculated. This RfC for
chronic health effects is 0.9 ppb, or
about 2 µg/m3. Confidence in the
inhalation RfC is medium.
c. Formaldehyde
Since 1987, EPA has classified
formaldehyde, a hydrocarbon, as a
49 U.S. EPA. (2002). Health Assessment of 1,3Butadiene. Office of Research and Development,
National Center for Environmental Assessment,
Washington Office, Washington, DC. Report No.
EPA600–P–98–001F. https://cfpub.epa.gov/ncea/
cfm/recordisplay.cfm?deid=54499.
50 U.S. EPA (1998). A Science Advisory Board
Report: Review of the Health Risk Assessment of
1,3-Butadiene. EPA–SAB–EHC–98.
51 Delzell, E, N. Sathiakumar, M. Macaluso, et al.
(1995). A follow-up study of synthetic rubber
workers. Submitted to the International Institute of
Synthetic Rubber Producers. University of Alabama
at Birmingham. October 2, 1995.
52 Bevan, C.; Stadler, J.C.; Elliot, G.S.; et al. (1996)
Subchronic toxicity of 4-vinylcyclohexene in rats
and mice by inhalation. Fundam. Appl. Toxicol.
32:1–10.
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probable human carcinogen based on
evidence in humans and in rats, mice,
hamsters, and monkeys.53 Recently
released research conducted by the
National Cancer Institute (NCI) found an
increased risk of nasopharyngeal cancer
among workers exposed to
formaldehyde.54 55 A recent National
Institute of Occupational Safety and
Health (NIOSH) study of garment
workers also found increased risk of
death due to leukemia among workers
exposed to formaldehyde.56 In 2004, the
working group of the International
Agency for Research on Cancer
concluded that formaldehyde is
carcinogenic to humans (Group 1
classification), on the basis of sufficient
evidence in humans and sufficient
evidence in experimental animals—a
higher classification than previous IARC
evaluations. In addition, the National
Institute of Environmental Health
Sciences recently nominated
formaldehyde for reconsideration as a
known human carcinogen under the
National Toxicology Program. Since
1981 it has been listed as a ‘‘reasonably
anticipated human carcinogen.’’
In the past 15 years there has been
substantial research on the inhalation
dosimetry for formaldehyde in rodents
and primates by the CIIT Centers for
Health Research, with a focus on use of
rodent data for refinement of the
quantitative cancer dose-response
assessment.57 58 59 CIIT’s risk assessment
of formaldehyde incorporated
mechanistic and dosimetric information
on formaldehyde. The risk assessment
analyzed carcinogenic risk from inhaled
53 U.S. EPA (1987). Assessment of Health Risks to
Garment Workers and Certain Home Residents from
Exposure to Formaldehyde, Office of Pesticides and
Toxic Substances, April 1987.
54 Hauptmann, M.; Lubin, J. H.; Stewart, P. A.;
Hayes, R. B.; Blair, A. 2003. Mortality from
lymphohematopoetic malignancies among workers
in formaldehyde industries. Journal of the National
Cancer Institute 95: 1615–1623.
55 Hauptmann, M.; Lubin, J. H.; Stewart, P. A.;
Hayes, R. B.; Blair, A. 2004. Mortality from solid
cancers among workers in formaldehyde industries.
American Journal of Epidemiology 159: 1117–1130.
56 Pinkerton, L. E. 2004. Mortality among a cohort
of garment workers exposed to formaldehyde: an
update. Occup. Environ. Med. 61: 193–200.
57 Conolly, RB, JS Kimbell, D Janszen, PM
Schlosser, D Kalisak, J Preston, and FJ Miller. 2003.
Biologically motivated computational modeling of
formaldehyde carcinogenicity in the F344 rat. Tox.
Sci. 75: 432–447.
58 Conolly, RB, JS Kimbell, D Janszen, PM
Schlosser, D Kalisak, J Preston, and FJ Miller. 2004.
Human respiratory tract cancer risks of inhaled
formaldehyde: Dose-response predictions derived
from biologically-motivated computational
modeling of a combined rodent and human dataset.
Tox. Sci. 82: 279–296.
59 Chemical Industry Institute of Toxicology
(CIIT). 1999. Formaldehyde: Hazard
characterization and dose-response assessment for
carcinogenicity by the route of inhalation. CIIT,
September 28, 1999. Research Triangle Park, NC.
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formaldehyde using approaches that are
consistent with EPA’s draft guidelines
for carcinogenic risk assessment. In
2001, Environment Canada relied on
this cancer dose-response assessment in
their assessment of formaldehyde.60 In
2004, EPA also relied on this cancer
unit risk estimate during the
development of the plywood and
composite wood products national
emissions standards for hazardous air
pollutants (NESHAPs).61 In these rules,
EPA concluded that the CIIT work
represented the best available
application of the available mechanistic
and dosimetric science on the doseresponse for portal of entry cancers due
to formaldehyde exposures. EPA is
reviewing the recent work cited above
from the NCI and NIOSH, as well as the
analysis by the CIIT Centers for Health
Research and other studies, as part of a
reassessment of the human hazard and
dose-response associated with
formaldehyde.
Noncancer effects of formaldehyde
have been observed in humans and
several animal species and include
irritation to eye, nose and throat tissues
in conjunction with increased mucous
secretions.
d. Acetaldehyde
Acetaldehyde, a hydrocarbon, is
classified in EPA’s IRIS database as a
probable human carcinogen and is
considered moderately toxic by
inhalation.62 Based on nasal tumors in
rodents, the upper confidence limit
estimate of a lifetime extra cancer risk
from continuous acetaldehyde exposure
is about 2.2×10¥6 per µg/m3. In other
words, it is estimated that about 2
persons in one million exposed to 1 µg/
m3 acetaldehyde continuously for their
lifetime (70 years) would develop
cancer as a result of their exposure,
although the risk could be as low as
zero. In short-term (4 week) rat studies,
compound-related histopathological
changes were observed only in the
respiratory system at various
concentration levels of exposure.63 64
60 Health Canada. 2001. Priority Substances List
Assessment Report. Formaldehyde. Environment
Canada, Health Canada, February 2001.
61 U.S. EPA. 2004. National Emission Standards
for Hazardous Air Pollutants for Plywood and
Composite Wood Products Manufacture: Final Rule.
(69 FR 45943, 7/30/04).
62 U.S. EPA. 1988. Integrated Risk Information
System File of Acetaldehyde. This material is
available electronically at https://www.epa.gov/iris/
subst/0290.htm.
63 Appleman, L. M., R. A. Woutersen, V. J. Feron,
R. N. Hooftman, and W. R. F. Notten. (1986). Effects
of the variable versus fixed exposure levels on the
toxicity of acetaldehyde in rats. J. Appl. Toxicol. 6:
331–336.
64 Appleman, L.M., R.A. Woutersen, and V.J.
Feron. (1982). Inhalation toxicity of acetaldehyde in
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Data from these studies showing
degeneration of the olfactory epithelium
were found to be sufficient for EPA to
develop an RfC for acetaldehyde of 9 µg/
m3. Confidence in the principal study is
medium and confidence in the database
is low, due to the lack of chronic data
establishing a no observed adverse effect
level and due to the lack of reproductive
and developmental toxicity data.
Therefore, there is low confidence in the
RfC. The agency is currently conducting
a reassessment of risk from inhalation
exposure to acetaldehyde.
The primary acute effect of exposure
to acetaldehyde vapors is irritation of
the eyes, skin, and respiratory tract.65
Some asthmatics have been shown to be
a sensitive subpopulation to decrements
in functional expiratory volume (FEV1
test) and bronchoconstriction upon
acetaldehyde inhalation.66
e. Acrolein
Acrolein, a hydrocarbon, is intensely
irritating to humans when inhaled, with
acute exposure resulting in upper
respiratory tract irritation and
congestion. The Agency has developed
an RfC for acrolein of 0.02 µg/m3.67 The
overall confidence in the RfC
assessment is judged to be medium. The
Agency is also currently in the process
of conducting an assessment of acute
health effects for acrolein. EPA
determined in 2003 using the 1999 draft
cancer guidelines that the human
carcinogenic potential of acrolein could
not be determined because the available
data were inadequate. No information
was available on the carcinogenic effects
of acrolein in humans and the animal
data provided inadequate evidence of
carcinogenicity.
f. Polycyclic Organic Matter (POM)
POM is generally defined as a large
class of organic compounds which have
multiple benzene rings and a boiling
point greater than 100 degrees Celsius.
Many of the compounds included in the
class of compounds known as POM are
classified by EPA as probable human
carcinogens based on animal data. One
rats. I. Acute and subacute studies. Toxicology. 23:
293–297.
65 U.S. EPA (1988). Integrated Risk Information
System File of Acetaldehyde. This material is
available electronically at https://www.epa.gov/iris/
subst/0290.htm.
66 Myou, S.; Fujimura, M.; Nishi K.; Ohka, T.; and
Matsuda, T. (1993) Aerosolized acetaldehyde
induces histamine-mediated bronchoconstriction in
asthmatics. Am. Rev. Respir.Dis.148(4 Pt 1): 940–3.
67 U.S. Environmental Protection Agency (2003)
Integrated Risk Information System (IRIS) on
Acrolein. National Center for Environmental
Assessment, Office of Research and Development,
Washington, D.C. 2003. This material is available
electronically at https://www.epa.gov/iris/subst/
0364.htm.
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of these compounds, naphthalene, is
discussed separately below.
Polycyclic aromatic hydrocarbons
(PAHs) are a chemical subset of POM.
In particular, EPA frequently obtains
data on 16 of these POM compounds.
Recent studies have found that maternal
exposures to PAHs in a population of
pregnant women were associated with
several adverse birth outcomes,
including low birth weight and reduced
length at birth.68 These studies are
discussed in the Regulatory Impact
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g. Naphthalene
Naphthalene is a PAH compound
consisting of two benzene rings fused
together with two adjacent carbon atoms
common to both rings. In 2004, EPA
released an external review draft
(External Review Draft, IRIS
Reassessment of the Inhalation
Carcinogenicity of Naphthalene, U.S.
EPA. https://www.epa.gov/iris) of a
reassessment of the inhalation
carcinogenicity of naphthalene.69 The
draft reassessment completed external
peer review in 2004 by Oak Ridge
Institute for Science and Education.70
Based on external comments, additional
analyses are being considered.
California EPA has also released a new
risk assessment for naphthalene with a
cancer unit risk estimate of 3×10¥5 per
µg/m3.71 The California EPA value was
used in the 1999 NATA and in the
analyses done for this rule. In addition,
IARC has reevaluated naphthalene and
re-classified it as Group 2B: possibly
carcinogenic to humans.72 The cancer
data form the basis of an inhalation RfC
of 3 µg/m3.73 A low to medium
confidence rating was given to this RfC,
in part because it cannot be said with
68 Perara, F.P.; Rauh, V.; Tsai, W–Y.; et al. (2002)
Effect of transplacental exposure to environmental
pollutants on birth outcomes in a multiethnic
population. Environ Health Perspect. 111: 201–205.
69 U.S. EPA. (2004) External Review Draft, IRIS
Reassessment of the Inhalation Carcinogenicity of
Naphthalene. https://www.epa.gov/iris
70 Oak Ridge Institute for Science and Education.
(2004) External Peer Review for the IRIS
Reassessment of the Inhalation Carcinogenicity of
Naphthalene. August 2004. https://cfpub2.epa.gov/
ncea/cfm/recordisplay.cfm?deid=86019
71 California EPA. (2004) Long Term Health
Effects of Exposure to Naphthalene. Office of
Environmental Health Hazard Assessment. https://
www.oehha.ca.gov/air/toxic_contaminants/
draftnaphth.html
72 International Agency for Research on Cancer
(IARC). (2002) Monographs on the Evaluation of the
Carcinogenic Risk of Chemicals for Humans. Vol.
82. Lyon, France.
73 EPA 2005 ‘‘Full IRIS Summary for Naphthalene
(CASRN 91–20–3)’’ Environmental Protection
Agency, Integrated Risk Information System (IRIS),
Office of Health and Environmental Assessment,
Environmental Criteria and Assessment Office,
Cincinnati, OH https://www.epa.gov/iris/subst/
0436.htm.
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certainty that this RfC will be protective
for hemolytic anemia and cataracts, the
more well-known human effects from
naphthalene exposure.
h. Diesel Particulate Matter and Diesel
Exhaust Organic Gases
In EPA’s Diesel Health Assessment
Document (HAD),74 diesel exhaust was
classified as likely to be carcinogenic to
humans by inhalation at environmental
exposures, in accordance with the
revised draft 1996/1999 EPA cancer
guidelines. A number of other agencies
(National Institute for Occupational
Safety and Health, the International
Agency for Research on Cancer, the
World Health Organization, California
EPA, and the U.S. Department of Health
and Human Services) have made similar
classifications. EPA concluded in the
Diesel HAD that it is not possible
currently to calculate a cancer unit risk
for diesel exhaust due to a variety of
factors that limit the current studies,
such as limited quantitative exposure
histories in occupational groups
investigated for lung cancer.
However, in the absence of a cancer
unit risk, the EPA Diesel HAD sought to
provide additional insight into the
significance of the cancer hazard by
estimating possible ranges of risk that
might be present in the population. The
possible risk range analysis was
developed by comparing a typical
environmental exposure level for
highway diesel sources to a selected
range of occupational exposure levels.
The occupationally observed risks were
then proportionally scaled according to
the exposure ratios to obtain an estimate
of the possible environmental risk. A
number of calculations are needed to
accomplish this, and these can be seen
in the EPA Diesel HAD. The outcome
was that environmental risks from
diesel exhaust exposure could range
from a low of 10¥4 to 10¥5 to as high
as 10¥3, reflecting the range of
occupational exposures that could be
associated with the relative and absolute
risk levels observed in the occupational
studies. Because of uncertainties, the
analysis acknowledged that the risks
could be lower than 10¥4 or 10¥5, and
a zero risk from diesel exhaust exposure
was not ruled out.
The acute and chronic exposurerelated effects of diesel exhaust
emissions are also of concern to the
Agency. EPA derived an RfC from
consideration of four well-conducted
74 U.S. EPA (2002) Health Assessment Document
for Diesel Engine Exhaust. EPA/600/8–90/057F
Office of Research and Development, Washington
DC. This document is available electronically at
https://cfpub.epa.gov/ncea/cfm/
recordisplay.cfm?deid=29060.
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chronic rat inhalation studies showing
adverse pulmonary effects.75 76 77 78 The
RfC is 5 µg/m3 for diesel exhaust as
measured by diesel PM. This RfC does
not consider allergenic effects such as
those associated with asthma or
immunologic effects. There is growing
evidence, discussed in the Diesel HAD,
that diesel exhaust can exacerbate these
effects, but the exposure-response data
are presently lacking to derive an RfC.
The Diesel HAD also briefly
summarizes health effects associated
with ambient PM and the EPA’s annual
National Ambient Air Quality Standard
(NAAQS) of 15 µg/m3. There is a much
more extensive body of human data
showing a wide spectrum of adverse
health effects associated with exposure
to ambient PM, of which diesel exhaust
is an important component. The RfC is
not meant to say that 5 µg/m3 provides
adequate public health protection for
ambient PM2.5. In fact, there may be
benefits to reducing diesel PM below 5
µg/m3 since diesel PM is a major
contributor to ambient PM2.5.
E. Gasoline PM
Beyond the specific areas of
quantifiable risk discussed above in
section III.C, EPA is also currently
investigating gasoline PM. Gasoline
exhaust is a complex mixture that has
not been evaluated in EPA’s IRIS, in
contrast to diesel exhaust, which has
been evaluated in IRIS. However, there
is evidence for the mutagenicity and
cytotoxicity of gasoline exhaust and
gasoline PM. Seagrave et al. investigated
the combined particulate and
semivolatile organic fractions of
gasoline engine emissions.79 Their
results demonstrate that emissions from
gasoline engines are mutagenic and can
induce inflammation and have cytotoxic
effects. Gasoline exhaust is a ubiquitous
75 Ishinishi, N; Kuwabara, N; Takaki, Y; et al.
(1988) Long-term inhalation experiments on diesel
exhaust. In: Diesel exhaust and health risks. Results
of the HERP studies. Ibaraki, Japan: Research
Committee for HERP Studies; pp. 11–84.
76 Heinrich, U; Fuhst, R; Rittinghausen, S; et al.
(1995) Chronic inhalation exposure of Wistar rats
and two different strains of mice to diesel engine
exhaust, carbon black, and titanium dioxide. Inhal.
Toxicol. 7:553–556.
77 Mauderly, JL; Jones, RK; Griffith, WC; et al.
(1987) Diesel exhaust is a pulmonary carcinogen in
rats exposed chronically by inhalation. Fundam.
Appl. Toxicol. 9:208–221.
78 Nikula, KJ; Snipes, MB; Barr, EB; et al. (1995)
Comparative pulmonary toxicities and
carcinogenicities of chronically inhaled diesel
exhaust and carbon black in F344 rats. Fundam.
Appl. Toxicol. 25:80–94.
79 Seagrave, J.; McDonald, J.D.; Gigliotti, A.P.;
Nikula, K.J.; Seilkop, S.K.; Gurevich, M. and
Mauderly, J.L. (2002) Mutagenicity and in Vivo
Toxicity of Combined Particulate and Semivolatile
Organic Fractions of Gasoline and Diesel Engine
Emissions. Toxicological Sciences 70:212–226.
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source of particulate matter,
contributing to the health effects
observed for ambient PM which is
discussed extensively in the EPA
Particulate Matter Criteria Document.80
The PM Criteria Document notes that
the PM components of gasoline and
diesel engine exhaust are hypothesized,
important contributors to the observed
increases in lung cancer incidence and
mortality associated with ambient
PM2.5.81 Gasoline PM is also a
component of near-roadway emissions
that may be contributing to the health
effects observed in people who live near
roadways (see section III.F).
EPA is working to improve the
understanding of PM emissions from
gasoline engines, including the potential
range of emissions and factors that
influence emissions. EPA led a
cooperative test program that recently
completed testing approximately 500
randomly procured vehicles in the
Kansas City metropolitan area. The
purpose of this study was to determine
the distribution of gasoline PM
emissions from the in-use light-duty
fleet. Results from this study are
expected to be available in 2006. Some
source apportionment studies show
gasoline and diesel PM can result in
larger contributions to ambient PM than
predicted by EPA emission
inventories.82 83 These source
apportionment studies were one
impetus behind the Kansas City study.
Another issue related to gasoline PM
is the effect of gasoline vehicles and
engines on ambient PM, especially
secondary PM. Ambient PM is
composed of primary PM emitted
directly into the atmosphere and
secondary PM that is formed from
chemical reactions in the atmosphere.
The issue of secondary organic aerosol
formation from aromatic precursors is
an important one to which EPA and
others are paying significant attention.
This is discussed in more detail in
Section 1.4.1 of the RIA.
80 U.S. Environmental Protection Agency (2004)
Air Quality Criteria for Particulate Matter. Research
Triangle Park, NC: National Center for
Environmental Assessment—RTP Office; Report No.
EPA/600/P–99/002aF (PM Criteria Document).
81 PM Criteria Document, p. 8–318.
82 Fujita, E.; Watson, M.J.; Chow, M.C.; et al.
(1998) Northern Front Range Air Quality Study,
Volume C: Source apportionment and simulation
methods and evaluation. Prepared for Colorado
State University, Cooperative Institute for Research
in the Atmosphere, by Desert Research Institute,
Reno, NV.
83 Schauer, J.J.; Rogge, W.F.; Hildemann, L.M.; et
al. (1996) Source apportionment of airborne
particulate matter using organic compounds as
tracers. Atmos. Environ. 30(22):3837–3855.
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F. Near-Roadway Health Effects
Over the years there have been a large
number of studies that have examined
associations between living near major
roads and different adverse health
endpoints. These studies generally
examine people living near heavilytrafficked roadways, typically within
several hundred meters, where fresh
emissions from motor vehicles are not
yet fully diluted with background air.
Several studies have measured
elevated concentrations of pollutants
emitted directly by motor vehicles near
road as compared to overall urban
background levels. These elevated
concentrations generally occur within
approximately 200 meters of the road,
although the distance may vary
depending on traffic and environmental
conditions. Pollutants measured with
elevated concentrations include
benzene, polycyclic aromatic
hydrocarbons, carbon monoxide,
nitrogen dioxide, black carbon, and
coarse, fine, and ultrafine particulate
matter. In addition, concentrations of
road dust, and wear particles from tire
and brake use also show concentration
increases in proximity of major
roadways.
The near-roadway health studies
provide stronger evidence for some
health endpoints than others. Evidence
of adverse responses to traffic-related
pollution is strongest for non-allergic
respiratory symptoms, cardiovascular
effects, premature adult mortality, and
adverse birth outcomes, including low
birth weight and size. Some evidence
for new onset asthma is available, but
not all studies have significant
orrelations. Lastly, among studies of
childhood cancer, in particular
childhood leukemia, evidence is
inconsistent. Several small studies
report positive associations, though
such effects have not been observed in
two larger studies. As described above,
benzene and 1,3-butadiene are both
known human leukemogens in adults.
As previously mentioned, there is
evidence of increased risk of leukemia
among children whose parents have
been occupationally exposed to
benzene. Though the near-roadway
studies are equivocal, taken together
with the laboratory studies and other
exposure environments, the data suggest
a potentially serious children’s health
concern could exist. Additional research
is needed to determine the significance
of this potential concern.
Significant scientific uncertainties
remain in our understanding of the
relationship between adverse health
effects and near-road exposure,
including the exposures of greatest
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concern, the importance of chronic
versus acute exposures, the role of fuel
type (e.g. diesel or gasoline) and
composition (e.g., % aromatics),
relevant traffic patterns, the role of costressors including noise and
socioeconomic status, and the role of
differential susceptibility within the
‘‘exposed’’ populations. For a more
detailed discussion, see Chapter 3 of the
Regulatory Impact Analysis.
These studies provide qualitative
evidence that reducing emissions from
on-road mobile sources will provide
public health benefits beyond those that
can be quantified using currently
available information.
G. How Would This Proposal Reduce
Emissions of MSATs?
The benzene and hydrocarbon
standards proposed in this action would
reduce benzene, 1,3-butadiene,
formaldehyde, acrolein, polycyclic
organic matter, and naphthalene, as well
as many other hydrocarbon compounds
that are emitted by motor vehicles,
including those that are listed in Table
III.B–1 and discussed in more detail in
Chapter 1 of the RIA. The emission
reductions expected from today’s
controls are reported in section V.E of
this preamble and Chapter 2 of the RIA.
EPA believes that the emission
reductions from the standards proposed
today for motor vehicles and their fuels,
combined with the standards currently
in place, represent the maximum
achievable reductions of emissions from
motor vehicles through the application
of technology that will be available,
considering costs and the other factors
listed in section 202(l)(2). This
conclusion applies whether you
consider just the compounds listed in
Table III.B–1, or consider all of the
compounds on the Master List of
emissions, given the breadth of EPA’s
current and proposed control programs
and the broad groups of emissions that
many of the control technologies
reduce.
EPA has already taken significant
steps to reduce diesel emissions from
mobile sources. We have adopted
stringent standards for on-highway
diesel trucks and buses, and nonroad
diesel engines (engines used, for
example, in construction, agricultural,
and industrial applications). We also
have additional programs underway to
reduce diesel emissions, including
voluntary programs and a proposal that
is being developed to reduce emissions
from diesel locomotives and marine
engines.
Emissions from motor vehicles can be
chemically categorized as hydrocarbons,
trace elements (including metals) and a
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few additional compounds containing
carbon, nitrogen and/or halogens (e.g.,
chlorine). For the hydrocarbons, which
are the vast majority of these
compounds, we believe that with the
controls proposed today, we would
control the emissions of these
compounds from motor vehicles to the
maximum amount currently feasible or
currently identifiable with available
information. Section VI of this preamble
provides more details about why the
proposed and existing standards
represent maximum achievable
reduction of hydrocarbons from motor
vehicles. There are not motor vehicle
controls to reduce individual
hydrocarbons selectively; instead, the
maximum emission reductions are
achieved by controls on hydrocarbons
as a group. There are fuel controls that
could selectively reduce individual air
toxics (e.g., formaldehyde,
acetaldehyde, 1,3-butadiene), as well as
controls that reduce hydrocarbons more
generally. Section VII of this preamble
describes why the standards we are
proposing today represent the maximum
emission reductions achievable through
fuel controls, considering the factors
required by Clean Air Act section 202(l).
Motor vehicle emissions also contain
trace elements, including metals, which
originate primarily from engine wear
and impurities in engine oil and
gasoline or diesel fuel. EPA does not
have authority to regulate engine oil,
and there are no feasible motor vehicle
controls to directly prevent engine wear.
Nevertheless, oil consumption and
engine wear have decreased over the
years, decreasing emission of metals
from these sources. Metals associated
with particulate matter will be captured
in emission control systems employing
a particulate matter trap, such as heavyduty vehicles meeting the 2007
standards. We believe that currently,
particulate matter traps, in combination
with engine-out control, represent the
maximum feasible reduction of both
motor vehicle particulate matter and
toxic metals present as a component of
the particulate matter.
The mobile source contribution to the
national inventory for metal compounds
is generally small. In fact, the emission
rate for most metals from motor vehicles
is small enough that quantitative
measurement requires state-of-the art
analytical techniques that are only
recently being applied to this source
category. We have efforts underway to
gather information regarding trace metal
emissions, including mercury
emissions, from motor vehicles (see
Chapter 1 of the RIA for more details).
A few metals and other elements are
used as fuel additives. These additives
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are designed to reduce the emission of
regulated pollutants either in
combination with or without an
emission control device (e.g., a passive
particulate matter trap). Clean Air Act
section 211 provides EPA with various
authorities to regulate fuel additives in
order to reduce the risk to public health
from exposure to their emissions. It is
under this section that EPA requires
manufacturers to register additives
before their introduction into
commerce. Registration involves certain
data requirements that enable EPA to
identify products whose emissions may
pose an unreasonable risk to public
health. In addition, section 211 provides
EPA with authority to require health
effects testing to fill any gaps in the data
that would prevent a determination
regarding the potential for risk to the
public. Clean Air Act section 211(c)
provides the primary mechanism by
which EPA would take actions
necessary to minimize exposure to
metals or other additives to diesel and
gasoline. It is under section 211 that
EPA is currently generating the
information needed to update an
assessment of the potential human
health risks related to having manganese
in the national fuel supply.
Existing regulations limit sulfur in
gasoline and diesel fuel to the maximum
amount feasible and will reduce
emissions of all sulfur-containing
compounds (e.g., hydrogen sulfide,
carbon disulfide) to the greatest degree
achievable.84 85 86 For the remaining
compounds (e.g., chlorinated
compounds), we currently have very
little information regarding emission
rates and conditions that impact
emissions. This information would be
necessary in order to evaluate potential
controls under section 202(l). Emissions
of hydrocarbons containing chlorine
(e.g., dioxins/furans) would likely be
reduced with control measures that
reduce total hydrocarbons, just as these
emissions were reduced with the use of
catalytic controls that lowered exhaust
hydrocarbons.
IV. What Are the Air Quality and
Health Impacts of Air Toxics, and How
Do Mobile Sources Contribute?
A. What Is the Health Risk to the U.S.
Population from Inhalation Exposure to
Ambient Sources of Air Toxics, and
How Would It be Reduced by the
Proposed Controls?
EPA’s National-Scale Air Toxics
Assessment (NATA) assesses human
84 65
FR 6697, February 10, 2000.
FR 5001, January 18, 2001.
86 69 FR 38958, June 29, 2004.
85 66
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health impacts from chronic inhalation
exposures to outdoor sources of air
toxics. It assesses lifetime risks
assuming continuous exposure to levels
of air toxics estimated for a particular
point in time. The most recent NATA
was done for the year 1999.87
The NATA modeling framework has a
number of limitations, but it remains
very useful in identifying air toxic
pollutants and sources of greatest
concern. Among the significant
limitations of the framework, which are
discussed in more detail in the
regulatory impact analysis, is that it
cannot be used to reliably identify ‘‘hot
spots,’’ such as areas in immediate
proximity to major roads, where the air
concentration, exposure and/or risk
might be significantly higher within a
census tract 88 or county. These ‘‘hot
spots’’ are discussed in more detail in
section IV.B.2. The framework also does
not account for risk from sources of air
toxics originating indoors, such as
stoves, out-gassing from building
materials, or evaporative benzene
emissions from cars in attached garages.
There are also limitations associated
with the dose-response values used to
quantify risk; these are discussed in
Section I of the preamble. Importantly,
it should be noted that the 1999 NATA
does not include default adjustments for
early life exposures recently
recommended in the Supplemental
Guidance for Assessing Susceptibility
from Early-Life Exposure to
Carcinogens.89 These adjustments
would be applied to compounds which
act through a mutagenic mode of action.
EPA will determine as part of the IRIS
assessment process which substances
meet the criteria for making
adjustments, and future assessments
will reflect them. If warranted,
incorporation of such adjustments
would lead to higher estimates of risk
assuming constant lifetime exposure.
Because of its limitations, EPA notes
that the NATA assessment should not
be used as the basis for developing risk
reduction plans or regulations to control
specific sources or pollutants.
Additionally, this assessment should
not be used for estimating risk at the
local level, for quantifying benefits of
reduced air toxic emissions, or for
identifying localized hotspots. In this
87 www.epa.gov/ttn/atw/nata1999.
88 A census tract is a subdivision of a county that
typically contains roughly 4000 people. In urban
areas, these tracts can be very small, on the order
of a city block, whereas in rural areas, they can be
large.
89 U. S. EPA. (2005) Supplemental Guidance for
Assessing Susceptibility from Early-Life Exposure
to Carcinogens. Report No. EPA/630/R–03/003F.
Available electronically at https://cfpub.epa.gov/
ncea/cfm/recordisplay.cfm?deid=116283.
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rule, we have evaluated air quality,
exposure, and risk impacts of mobile
source air toxics using the 1999 NATA,
as well as projections of risk to future
years using the same tools as 1999
NATA. In addition, we also evaluate
more refined local scale modeling,
measured ambient concentrations,
personal exposure measurements, and
other data. This information is
discussed below, as well as in Chapter
3 of the RIA. It serves as a perspective
on the possible risk-related implications
of the rule.
Overall, the average nationwide
lifetime population cancer risk in 1999
NATA was 42 in a million, assuming
continuous exposure to 1999 levels. The
average noncancer respiratory hazard
index was 6.4.90 Highway vehicles and
nonroad equipment account for almost
50% of the average population cancer
risk, and 74% of the noncancer risk
These estimates are based on the
contribution of sources within 50
kilometers of a given emission point and
do not include the contribution to
ambient concentrations from transport
beyond 50 kilometers. Ambient
concentrations from transport beyond
50 kilometers, referred to as
‘‘background’’ in NATA, are responsible
for almost 50% of the average cancer
risk in NATA.
Section III.C.1 discusses the
pollutants that the 1999 National-Scale
Air Toxics Assessment identifies as
national and regional risk drivers. As
summarized in Table III.C–1, benzene is
the only pollutant described as a
national cancer risk driver. Twenty-four
percent of the total cancer risk in the
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90 A hazard index above 1 indicates the potential
for adverse health effects. It cannot be translated
into a probability that an adverse effect will occur,
and is not likely to be proportional to risk. A hazard
index greater than one can be best described as only
indicating that a potential may exist for adverse
health effects.
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1999 National-Scale Air Toxics
Assessment was due to benzene. In
1999, 68% of nationwide benzene
emissions were attributable to mobile
sources. 1,3-Butadiene and naphthalene
are regional cancer risk drivers that have
a large mobile source contribution. As
presented in Table III.C–2, 58% of
nationwide 1,3-butadiene emissions in
1999 came from mobile sources.
Twenty-seven percent of nationwide
naphthalene emissions in 1999 came
from mobile sources.
One compound, acrolein, was
identified as a national risk driver for
noncancer health effects, and 25% of
primary acrolein emissions were
attributable to mobile sources. Over
70% of the average ambient
concentration of acrolein is attributable
to mobile sources. This is due to the
large contribution from mobile source
1,3-butadiene, which is transformed to
acrolein in the atmosphere.
Table III.C–2 provides additional
information on the mobile source
contribution to emissions of national
and regional risk drivers. The standards
proposed in this rule will reduce
emissions of all these pollutants.
In addition to the 1999 NATA, we
have estimated future-year risks for
those pollutants included in the 1999
NATA whose emissions inventories
include a mobile source contribution
(see Table IV.B–1). This analysis
indicates that cancer and noncancer risk
will continue to be a public health
concern due to exposure to mobilesource-related pollutants.
Figure IV.A–1 summarizes changes in
average population inhalation cancer
risk for the MSATs in Table IV.A–1.
Despite significant reductions in risk
from these pollutants, average
inhalation cancer risks are expected to
remain well above 1 in 100,000. In
addition, because of population growth
(using projected populations from the
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U.S. Bureau of Census), the number of
Americans above the 1 in 100,000
cancer risk level from exposure to these
mobile source air toxics is projected to
increase from about 214 million in 1999
to 240 million in 2030. Benzene
continues to account for a large fraction
of the total inhalation cancer risk from
mobile source air toxics, decreasing
slightly from 45% of the risk in 1999 to
37% in 2030. Similarly, although the
average noncancer respiratory hazard
index for MSATs decreases from over 6
in 1999 to 3.2 in 2030, the population
with a hazard index above one increases
from 250 million in 1999 to 273 million
in 2030. That is, in 2030 nearly the
entire U.S. population will still be
exposed to levels of these pollutants
that have the potential to cause adverse
respiratory health effects (other than
cancer).
These projected risks were estimated
using the same tools and methods as the
1999 NATA, but with future-year
projected inventories. More detailed
information on the methods used to do
these projections, and associated
limitations and uncertainties, can be
found in Chapter 3 of the RIA for this
rule. Projected risks assumed 1999
‘‘background’’ levels. For MSATs,
‘‘background’’ accounts for slightly less
than 20% of the average cancer risk in
1999, increasing to 24% in 2030.
However, background levels should
decrease along with emissions. A
sensitivity analysis of this assumption is
presented in Chapter 3 of the RIA. It
should also be noted that the projected
inventories used for this modeling do
not include some more recent revisions,
such as higher emissions of
hydrocarbons, including gaseous air
toxics, at cold temperatures. These
revisions are discussed in section V and
increase the overall magnitude of the
inventory.
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from 1999 to 2030. Table IV.B–1 gives
TABLE IV.A–1.—POLLUTANTS INCLUDED IN RISK MODELING FOR the median and 5th and 95th percentile
cancer risk distributions for mobile
PROJECTION YEARS *—Continued
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Anthracene ** ....................
Benzene ...........................
Benz(a)anthracene ** .......
Benzo(a)pyrene ** ............
Benzo(b)fluoranthene ** ...
Benzo(g,h,i)perylene ** .....
Benzo(k)fluoranthene ** ....
Chromium (includes Chromium III, Chromium VI,
and non-speciated
Chromium).
Chrysene ** .......................
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Ethyl Benzene
Fluoranthene **
Fluorene **
Formaldehyde
Hexane
Indeno(1,2,3,c,d)pyrene **
Manganese
Methyl tert-butyl
ether (MTBE)
Naphthalene
Nickel
Phenanthrene **
Propionaldehyde
Pyrene **
Styrene
Toluene
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Dibenzo(a,h)anthracene **
Xylenes
* This list includes compounds from the
1999 National-Scale Air Toxics Assessment
with a mobile source emissions contribution,
for which data were sufficient to develop an
emissions inventory.
** POM compound as discussed in Section
III.
B. What Is the Distribution of Exposure
and Risk?
1. Distribution of National-Scale
Estimates of Risk From Air Toxics
National-scale modeling indicates that
95th percentile average cancer risk from
exposure to mobile source air toxics is
more than three times higher than
median risk. In addition, the 95th
percentile cancer risk is more than 10
times higher than the 5th percentile
risk. This is true for all years modeled,
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source air toxics. As previously
mentioned, the tools used in this
assessment are inadequate for
identifying ‘‘hot spots’’ and do not
account for significant sources of
inhalation exposure, such as benzene
emissions within attached garages from
vehicles, equipment, and portable fuel
containers. If these hot spots and
additional sources of exposure were
accounted for, a larger percentage of the
population would be exposed to higher
risk levels. (Sections IV.B.2–4 provides
more details on ‘‘hot spots’’ and the
implications for distribution of risk.) In
addition, the modeling underestimates
the contribution of hydrocarbon and
particulate matter emissions at cold
temperatures. These modeling results
are discussed in more detail in Chapter
3 of the RIA.
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TABLE IV.A–1.—POLLUTANTS INCLUDED IN RISK MODELING FOR
PROJECTION YEARS *
1,3-Butadiene ...................
2,2,4-Trimethylpentane ....
Acenaphthene ** ...............
Acenaphthylene ** ............
Acetaldehyde ....................
Acrolein ............................
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TABLE IV.B—1.—MEDIAN AND 5TH AND 95TH PERCENTILE LIFETIME INHALATION CANCER RISK DISTRIBUTIONS FOR
INHALATION EXPOSURE TO OUTDOOR SOURCES OF MOBILE SOURCE AIR TOXICS
[Based on modeled average census tract risks]
1999
2020
Pollutant
5th
All MSATs ....................................................................................
Benzene .......................................................................................
1,3-Butadiene ...............................................................................
Acetaldehyde ...............................................................................
Naphthalene .................................................................................
2. Elevated Concentrations and
Exposure in Mobile Source-Impacted
Areas
Air quality measurements near roads
often identify elevated concentrations of
air toxic pollutants at these locations.
The concentrations of air toxic
pollutants near heavily trafficked roads,
as well as the pollutant composition and
characteristics, differ from those
measured distant from heavily trafficked
roads. Exposures for populations
residing, working, or going to school
near major roads are likely higher than
for other populations. The vehicle and
fuel standards proposed in this rule will
reduce those elevated exposures.
Following is an overview of
concentrations of air toxics and
exposure to air toxics in areas heavily
impacted by mobile source emissions.
a. Concentrations Near Major Roadways
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The 1999 NATA estimates average
concentrations within a census tract, but
it does not differentiate between
locations near roadways and those
further away (within the same tract).
Local-scale modeling can better
characterize distributions of
concentrations, using more refined
allocation of highway vehicle emissions.
Urban-scale assessments done in
Houston, TX and Portland, OR
illustrated steep gradients of air toxic
concentrations along major roadways, as
well as better agreement with monitor
data.91–92 93 Results of the Portland study
show average concentrations of motor
vehicle-related pollutants are ten times
higher at 50 meters from a road than
they are at greater than 400 meters a
road. These findings are consistent with
pollutant dispersion theory, which
91–92 Kinnee, E.J.; Touma, J.S.; Mason, R.;
Thurman, J.; Beidler, A., Bailey, C.; Cook, R. (2004)
Allocation of onroad mobile emissions to road
segments for air toxics modeling in an urban area.
Transport. Res. Part D 9: 139–150.
93 Cohen, J.; Cook, R.; Bailey, C.R.; Carr, E. (2005)
Relationship between motor vehicle emissions of
hazardous pollutants, roadway proximity, and
ambient concentrations in Portland, Oregon.
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predicts that pollutants emitted along
roadways will show highest
concentrations nearest a road, and
concentrations exponentially decrease
with increasing distance downwind.
These near-road pollutant gradients
have been confirmed by measurements
of both criteria pollutants and air toxics,
and they are discussed in detail in
Chapter 3 of the RIA.
Air quality monitoring is another
means of evaluating pollutant
concentrations at locations near sources
such as roadways. It is also used to
evaluate model performance at a given
point and, given adequate data quality,
can be statistically analyzed to
determine associations with different
source types. EPA has been deploying
fixed-site ambient monitors that monitor
concentrations of multiple air toxics,
including benzene, over time. Several
studies have found that concentrations
of benzene and other mobile source air
toxics are significantly elevated near
busy roads compared to ‘‘urban
background’’ concentrations measured
at a fixed site. These studies are
discussed in detail in Chapter 3 of the
RIA.
Ambient VOC concentrations were
measured around residences in
Elizabeth, NJ, as part of the Relationship
among Indoor, Outdoor, and Personal
Air (RIOPA) study. Data from that study
was analyzed to assess how
concentrations are influenced by
proximity to known ambient emission
sources.94 95 The ambient concentrations
of benzene, toluene, ethylbenzene, and
xylene isomers (BTEX) were found to be
94 Kwon, J. (2005) Development of a RIOPA
database and evaluation of the effect of proximity
on the potential residential exposure to VOCs from
ambient sources. Rutgers, the State University of
New Jersey and University of Medicine and
Dentistry of New Jersey. PhD dissertation. This
document is available in Docket EPA–HQ–OAR–
2005–0036.
95 Weisel, C.P. (2004) Assessment of the
contribution to personal exposures of air toxics
from mobile sources. Final report. Submitted to
EPA Office of Transportation and Air Quality.
Environmental & Occupational Health Sciences
Institute, Piscataway, NJ. This document is
available in Docket EPA–HQ–OAR–2005–0036.
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inversely associated with distances to
interstate highways and major urban
roads, and with distance to gasoline
stations. The data indicate that BTEX
concentrations around homes within
200 meters of roadways and gas stations
are 1.5 to 4 times higher than urban
background levels.
b. Exposures Near Major Roadways
The modeling assessments and air
quality monitoring studies discussed
above have increased our understanding
of ambient concentrations of mobile
source air toxics and potential
population exposures. Results from the
following exposure studies reveal that
populations spending time near major
roadways likely experience elevated
personal exposures to motor vehicle
related pollutants. In addition, these
populations may experience exposures
to differing physical and chemical
compositions of certain air toxic
pollutants depending on the amount of
time spent in close proximity to motor
vehicle emissions. Following is a
detailed discussion on exposed
populations near major roadways.
i. Vehicles
Several studies suggest that
significant exposures may be
experienced while driving in vehicles.
A recent in-vehicle monitoring study
was conducted by EPA and consisted of
in-vehicle air sampling throughout work
shifts within ten police patrol cars used
by the North Carolina State Highway
Patrol (smoking not permitted inside the
vehicles).96 Troopers operated their
vehicles in typical patterns, including
highway and city driving and refueling.
In-vehicle benzene concentrations
averaged 12.8 µg/m3, while
concentrations measured at an
‘‘ambient’’ site located outside a nearby
state environmental office averaged 0.32
µg/m3. The study also found that the
benzene concentrations were closely
96 Riediker, M.; Williams, R.; Devlin, R.; et al.
(2003) Exposure to particulate matter, volatile
organic compounds, and other air pollutants inside
patrol cars. Environ Sci. Technol. 37: 2084–2093.
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associated with other fuel-related VOCs
measured.
In Boston, the exposure of commuters
to VOCs during various commuting
modes was examined.97 For commuters
driving a car, the mean time-weighted
concentrations of benzene, toluene, and
xylenes in-vehicle were measured at
17.0, 33.1, and 28.2 µg/m3, respectively.
The American Petroleum Institute
funded a screening study of high-end
exposure microenvironments as
required by section 211(b) of the Clean
Air Act.98 The study included vehicle
chase measurements and measurements
in several vehicle-related
microenvironments in several cities for
benzene and other air toxics. In-vehicle
microenvironments (average benzene
concentrations in parentheses) included
the vehicle cabin tested on congested
freeways (17.5 µg/m3), in parking
garages above-ground (155 µg/m3) and
below-ground (61.7 µg/m3), in urban
street canyons (7.54 µg/m3), and during
refueling (46.0 µg/m3).
In 1998, the California Air Resources
Board published an extensive study of
concentrations of in-vehicle air toxics in
Los Angeles and Sacramento, CA.99 The
data set is large and included a variety
of sampling conditions. On urban
freeways, benzene in-vehicle
concentrations ranged from 3 to 15 µg/
m3 in Sacramento and 10 to 22 µg/m3
in Los Angeles. In comparison, ambient
benzene concentrations ranged from 1 to
3 µg/m3 in Sacramento and 3 to 7 µg/
m3 in Los Angeles.
Similar findings of elevated
concentrations of pollutants have also
been found in studies done in diesel
buses.100 101 102
Overall, these studies show that
concentrations experienced by
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97 Chan
C.-C., Spengler J. D., Ozkaynak H., and
Lefkopoulou M. (1991) Commuter Exposures to
VOCs in Boston, Massachusetts. J. Air Waste
Manage. Assoc. 41: 1594–1600.
98 Zielinska, B.; Fujita, E.M.; Sagebiel, J.C.; et al.
(2002) Interim data report for Section 211(B) Tier
2 high end exposure screening study of baseline
and oxygenated gasoline. Prepared for American
Petroleum Institute. November 19, 2002. This
document is available in Docket EPA–HQ–OAR–
2005–0036.
99 Rodes, C.; Sheldon, L.; Whitaker, D.; et al.
(1998) Measuring concentrations of selected air
pollutants inside California vehicles. Final report to
California Air Resources Board. Contract No. 95–
339.
100 Fitz, D.R.; Winer, A.M.; Colome, S.; et al.
(2003) Characterizing the Range of Children’s
Pollutant Exposure During School Bus Commutes.
Prepared for the California Resources Board.
101 Sabin, L.D.; Behrentz, E.; Winer, A.M.; et al.
(2005) Characterizing the range of children’s air
pollutant exposure during school bus commutes. J.
Expos. Anal. Environ. Epidemiol. 15: 377–387.
102 Batterman, S.A.; Peng, C.Y.; and Braun, J.
(2002) Levels and composition of volatile organic
compounds on commuting routes in Detroit,
Michigan. Atmos. Environ. 36: 6015–6030.
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commuters and other roadway users are
substantially higher than those
measured in typical urban air. As a
result, the time a person spends in a
vehicle will significantly affect their
overall exposure.
ii. Homes and Schools
The proximity of schools to major
roads may result in elevated exposures
for children due to potentially increased
concentrations indoors and increased
exposures during outdoor activities.
Here we discuss international studies in
addition to the limited number of U.S.
studies, because while fleets and fuels
outside the U.S. can differ significantly,
the spatial distribution of
concentrations is relevant.
In the Fresno Asthmatic Children’s
Environment Study (FACES), trafficrelated pollutants were measured on
selected days from July 2002 to
February 2003 at a central site, and
inside and outside of homes and
outdoors at schools of asthmatic
children.103 Preliminary data indicate
that PAH concentrations are higher at
elementary schools located near primary
roads than at elementary schools distant
from primary roads (or located near
primary roads with limited access). PAH
concentrations also appear to increase
with increase in annual average daily
traffic on nearest major collector.
Remaining results regarding the
variance in traffic pollutant
concentrations at schools in relation to
proximity to roadways and traffic
density will be available in 2006.
The East Bay Children’s Respiratory
Health Study studied traffic-related air
pollution outside of schools near busy
roads in the San Francisco Bay Area in
2001.104 Concentrations of the traffic
pollutants PM10, PM2.5, black carbon,
total NOX, and NO2 were measured at 10
school sites in neighborhoods that
spanned a busy traffic corridor during
the spring and fall seasons. The school
sites were selected to represent a range
of locations upwind and downwind of
major roads. Differences were observed
in concentrations between schools
nearby (< 300 m) versus those more
distant (or upwind) from major roads.
Investigators found spatial variability in
exposure to black carbon, NOX, NO, and
(to a lesser extent) NO2, due specifically
to roads with heavy traffic within a
relatively small geographic area.
103 Personal communication with FACES
Investigators Fred Lurmann, Paul Roberts, and
Katharine Hammond. Data is currently being
prepared for publication.
104 Kim J.J.; Smorodinsky S.; Lipsett M.; et al.
(2004) Traffic-related air pollution near busy roads.
Am. J. Respir. Crit. Care Med. 170: 520–526.
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A study to assess children’s exposure
to traffic-related air pollution while
attending schools near motorways was
performed in the Netherlands.105
Investigators measured PM2.5, NO2 and
benzene inside and outside of 24
schools located within 400 m of
motorways. The indoor average benzene
concentration was 3.2 µg/m3 with a
range of 0.6–8.1 µg/m3. The outdoor
average benzene concentration was 2.2
µg/m3 with a range of 0.3–5.0 µg/m3.
Overall results indicate that indoor
pollutant concentrations are
significantly correlated with traffic
density and composition, percentage of
time downwind, and distance from
major roadways.
The Toxic Exposure Assessment—
Columbia/Harvard (TEACH) study
measured the concentrations of VOCs,
PM2.5, black carbon, and metals outside
the homes of high school students in
New York City.106 The study was
conducted during winter and summer of
1999 on 46 students and their homes.
Average winter (and summer) indoor
concentrations exceeded outdoor
concentrations by a factor of 2.3 (1.3). In
addition, analyses of spatial and
temporal patterns of MTBE
concentrations were consistent with
traffic patterns. MTBE is a tracer for
motor vehicle pollution.
Children are exposed to elevated
levels of air toxics not only in their
homes, classrooms, and outside on
school grounds, but also during their
commute to school. See the discussion
of in-vehicle concentrations of air toxics
above and in Chapter 3 of the RIA.
iii. Pedestrians and Bicyclists
Researchers have noted that
pedestrians and cyclists along major
roads experience elevated exposures to
motor vehicle related pollutants.
Although commuting near roadways
leads to higher levels of exposure to
traffic pollutants, the general consensus
is that exposure levels of those
commuting by walking or biking is
lower than for those who travel by car
or bus, (see discussion on in-vehicle
exposure in previous section above).
These studies are discussed in Chapter
3 of the RIA for this rule.
105 Janssen, N.A.H.; van Vliet, P.H.N.; Aarts, F.; et
al. (2001) Assessment of exposure to traffic related
air pollution of children attending schools near
motorways. Atmos. Environ. 35: 3875–3884.
106 Kinney, P.L.; Chillrud, S.N.; Ramstrom, S.; et
al. (2002) Exposures to multiple air toxics in New
York City. Environ Health Perspect. 110 (Suppl 4):
539–546.
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c. Exposure and Concentrations in
Homes with Attached Garages
People living in homes with attached
garages are potentially exposed to
substantially higher concentrations of
benzene, toluene, and other VOCs
indoors. Homes with attached garages
present a special concern related to
infiltration of components of fuel,
exhaust, and other materials stored in
garages (including gasoline in gas cans).
A study from the early 1980’s found that
approximately 30% of an average
nonsmoker’s benzene exposure
originated from sources in attached
garages.107
Concentrations within garages are
often substantially higher than those
found outdoors or indoors. A recentlycompleted study in Michigan found that
average concentrations in residential
garages were 36.6 µg/m3, compared to
0.4 µg/m3 outdoors.108 A recent study in
Alaska, where fuel benzene
concentrations are higher, cold start
emissions are higher, and homes are
more tightly sealed than in most of the
U.S., found average garage
concentrations of 101 µg/m3.109 Air
passing from these high-benzene
locations can cause increased
concentrations indoors.
Measurement studies have found that
homes with attached garages can have
significantly higher concentrations of
benzene and other VOCs. One study
from Alaska found that in homes
without attached garages, average
benzene concentrations were 8.6 µg/m3,
while homes with attached garages had
average concentrations of 70.8 µg/m3.110
Another showed that indoor CO and
total hydrocarbon (THC) concentrations
rose sharply following a cold vehicle
starting and pulling out of the attached
garage, persisting for an hour or
more.111 The study also showed that
cold start emissions accounted for 13–
85% of indoor non-methane
107 Wallace, L. (1996) Environmental exposure to
benzene: an update. Environ Health Perspect. 104
(Suppl 6): 1129–1136.
108 Batterman, S.; Hatzivasilis, G.; Jia, C. (2006)
Concentrations and emissions of gasoline and other
vapors from residential vehicle garages. Atmos.
Environ. 30: 1828–1844.
109 George, M.; Kaluza, P.; Maxwell, B.; Moore, G.;
Wisdom, S. (2002) Indoor air quality & ventilation
strategies in new homes in Alaska. Alaska Building
Science Network. www.cchrc.org. This document is
available in Docket EPA–HQ–OAR–2005–0036.
110 Schlapia, A.; Morris, S. (1998) Architectural,
behavioral, and environmental factors associated
with VOCs in Anchorage homes. Proceedings of the
Air & Waste Management Associations 94th Annual
Conference. Paper 98–A504.
111 Graham, L.A.; Noseworthy, L.; Fugler, D.;
O’Leary, K.; Karman, D.; Grande, C. (2004)
Contribution of vehicle emissions from an attached
garage to residential indoor air pollution levels. J.
Air & Waste Manage. Assoc. 54: 563–584.
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hydrocarbons (NMHC), while hot soak
emissions accounted for 9–71% of
indoor NMHC. Numerous other studies
have shown associations between VOCs
in indoor air and the presence of
attached garages. These studies are
discussed in Chapter 3 of the RIA.
EPA has conducted a modeling
analysis to examine the influence of
attached garages on personal exposure
to benzene.112 The analysis modeled the
air flow between the outdoor
environment, indoor environment, and
the garage, and accounted for the
fraction of home air intake from the
garage. Compared to national average
exposure concentrations of 1.36 µg/m3
modeled for 1999 in the National-Scale
Air Toxics Assessment, which do not
account for emissions originating in
attached garages, average exposure
concentrations for people with attached
garages could more than double. For
additional details, see Chapter 3 of the
RIA.
Overall, emissions of VOCs within
attached garages result in substantially
higher concentrations of benzene and
other pollutants indoors. Proposed
reductions in fuel benzene content, new
standards for cold temperature exhaust
emissions during vehicle starts, and
reduced emissions from gas cans are all
expected to significantly reduce this
major source of exposure.
d. Occupational Exposure
Occupational settings can be
considered a microenvironment in
which exposure to benzene and other
air toxics can occur. Occupational
exposures to benzene from mobile
sources or fuels can be several orders of
magnitude greater than typical
exposures in the non-occupationally
exposed population. Several key
occupational groups include workers in
fuel distribution, storage, and tank
remediation; handheld and nonhandheld equipment operators; and
workers who operate gasoline-powered
engines such as snowmobiles and
ATV’s. Exposures in these occupational
settings are discussed in Chapter 3 of
the RIA.
In addition, some occupations require
that workers spend considerable time in
vehicles, which increases the time they
spend in a higher-concentration
microenvironment. In-vehicle
concentrations are discussed in a
previous section above.
112 Bailey, C. (2005) Additional contribution to
benzene exposure from attached garages.
Memorandum to the Docket. This document is
available in Docket EPA–HQ–OAR–2005–0036.
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3. What Are the Size and Characteristics
of Highly Exposed Populations?
A study of the populations in three
states (Colorado, Georgia, and New
York) indicated that more than half of
the population lives within 200 meters
of a major road.113 In addition, analysis
of data from the Census Bureau’s
American Housing Survey suggests that
approximately 37 million people live
within 300 feet of a 4- or more lane
highway, railroad, or airport. American
Housing Survey statistics, as well as
epidemiology studies, indicate that
those houses sited near major
transportation sources are more likely to
be lower in income or have minority
residents than houses not located near
major transportation sources. These data
are discussed in detail in Chapter 3 of
the RIA.
Other population studies also indicate
that a significant fraction of the
population resides in locations near
major roads. At present, the available
studies use different indicators of
‘‘major road’’ and of ‘‘proximity,’’ but
the estimates range from 12.4% of
student enrollment in California
attending schools within 150 meters of
roads with 25,000 vehicles per day or
more, to 13% of Massachusetts veterans
living within 50 meters of a road with
at least 10,000 vehicles per day.114 115
Using a more general definition of a
‘‘major road,’’ between 22% and 51% of
different study populations live near
such roads.
4. What Are the Implications for
Distribution of Individual Risk?
We have made revisions to HAPEM5,
which is the exposure model used in
our national-scale modeling, in order to
account for near-road impacts. The
effect of the updated model is best
understood as widening the distribution
of exposure, with a larger fraction of the
population being exposed to higher
benzene concentrations. Including the
effects of residence locations near roads
can result in exposures to some
individuals that are up to 50% higher
than those predicted by HAPEM5.
The revised model, HAPEM6, was run
for three states representing different
parts of the country. These areas are
intended to represent different
113 Major roads are defined as those roads defined
by the U.S. Census as one of the following: ‘‘limited
access highway,’’ ‘‘highway,’’ ‘‘major road,’’ or
‘‘ramp.’’
114 Green, R.S.; Smorodinsky, S.; Kim, J.J.;
McLaughlin, R.; Ostro, B. (2004) Proximity of
California public schools to busy roads. Environ.
Health Perspect. 112: 61–66.
115 Garshick, E.; Laden, F.; Hart, J.E.; Caron, A.
(2003) Residence near a major road and respiratory
symptoms in U.S. veterans. Epidemiol. 14: 728–736.
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geographies, development patterns, and
housing densities. The states modeled
include Georgia, Colorado, and New
York. Overall, these study results
indicate that proximity to major roads
can significantly increase personal
exposure for populations living near
major roads. These modeling tools will
be extended to a national scale for the
final rulemaking.
For details on the modeling study
with HAPEM6, refer to Chapter 3.2 of
the RIA. We used geographic
information systems to estimate the
population within each U.S. census
tract living at various distances from a
major road (within 75 meters; between
75 and 200 meters; or beyond 200
meters). An exposure gradient was
determined for people living in each
zone, based on dispersion modeling.116
These gradients were confirmed with
monitoring studies funded by EPA.117
The HAPEM5 model was updated to
account for elevated concentrations
within these defined distances from
roadways and the population living in
these areas.
C. Ozone
While the focus of this rule is on air
toxics, the proposed vehicle and gas can
standards will also help reduce volatile
organic compounds (VOCs), which are
precursors to ozone.
1. Background
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Ground-level ozone, the main
ingredient in smog, is formed by the
reaction of VOCs and nitrogen oxides
(NOX) in the atmosphere in the presence
of heat and sunlight. These pollutants,
often referred to as ozone precursors, are
emitted by many types of pollution
sources, such as highway and nonroad
motor vehicles and engines, power
plants, chemical plants, refineries,
makers of consumer and commercial
products, industrial facilities, and
smaller ‘‘area’’ sources. VOCs can also
be emitted by natural sources such as
vegetation. The gas can controls
proposed in this action would help
reduce VOC emissions by reducing
evaporation, permeation and spillage
from gas cans. The proposed vehicle
116 Cohen, J.; Cook, R.; Bailey, C.R.; Carr, E. (2005)
Relationship between motor vehicle emissions of
hazardous pollutants, roadway proximity, and
ambient concentrations in Portland, Oregon.
Environ Modelling & Software 20: 7–12.
117 Kwon, J. (2005) Development of a RIOPA
database and evaluation of the effect of proximity
on the potential residential exposure to VOCs from
ambient sources. PhD Dissertation. Rutgers, The
State University of New Jersey and University of
Medicine and Dentistry of New Jersey. Written
under direction of Dr. Clifford Weisel. This
document is available in Docket EPA–HQ–OAR–
2005–0036.
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controls will also reduce VOC
emissions; however, because these
reductions will occur at cold
temperatures the ozone benefits will be
limited.
The science of ozone formation,
transport, and accumulation is
complex.118 Ground-level ozone is
produced and destroyed in a cyclical set
of chemical reactions, many of which
are sensitive to temperature and
sunlight. When ambient temperatures
and sunlight levels remain high for
several days and the air is relatively
stagnant, ozone and its precursors can
build up and result in more ozone than
typically would occur on a single hightemperature day. Further complicating
matters, ozone also can be transported
into an area from pollution sources
found hundreds of miles upwind,
resulting in elevated ozone levels even
in areas with low VOC or NOX
emissions. As a result, differences in
VOC and NOX emissions contribute to
daily, seasonal, and yearly differences
in ozone concentrations across different
locations.
The current ozone National Ambient
Air Quality Standards (NAAQS) has an
8-hour averaging time. The 8-hour
ozone NAAQS, established by EPA in
1997, is based on well-documented
science demonstrating that more people
were experiencing adverse health effects
at lower levels of exertion, over longer
periods, and at lower ozone
concentrations than addressed by the
previous one-hour ozone NAAQS. It
addresses ozone exposures of concern
for the general population and
populations most at risk, including
children active outdoors, outdoor
workers, and individuals with preexisting respiratory disease, such as
asthma. The 8-hour ozone NAAQS is
met at an ambient air quality monitoring
site when the average of the annual
fourth-highest daily maximum 8-hour
average ozone concentration over three
years is less than or equal to 0.084 ppm.
2. Health Effects of Ozone
The health and welfare effects of
ozone are well documented and are
critically assessed in the EPA ozone
criteria document (CD) and EPA staff
paper.119 120 In August 2005, the EPA
118 U.S. EPA (1996). Air Quality Criteria for
Ozone and Related Photochemical Oxidants,
EPA600–P–93–004aF. This document is available in
Docket EPA–HQ–OAR–2005–0036.
119 U.S. EPA (1996). Air Quality Criteria for
Ozone and Related Photochemical Oxidants,
EPA600–P–93–004aF. This document is available in
Docket EPA–HQ–OAR–2005–0036.
120 U.S. EPA (1996) Review of National Ambient
Air Quality Standards for Ozone, Assessment of
Scientific and Technical Information, OAQPS Staff
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released the second external review
draft of a new ozone CD which is
scheduled to be released in final form in
February 2006.121 This document
summarizes the findings of the 1996
ozone criteria document and critically
assesses relevant new scientific
information which has emerged in the
past decade. Additional information on
health and welfare effects of ozone can
also be found in the draft RIA for this
proposal.
Ozone can irritate the respiratory
system, causing coughing, throat
irritation, and/or uncomfortable
sensation in the chest. Ozone can
reduce lung function and make it more
difficult to breathe deeply, and
breathing may become more rapid and
shallow than normal, thereby limiting a
person’s normal activity. Ozone can also
aggravate asthma, leading to more
asthma attacks that require a doctor’s
attention and/or the use of additional
medication. In addition, ozone can
inflame and damage the lining of the
lungs, which may lead to permanent
changes in lung tissue, irreversible
reductions in lung function, and a lower
quality of life if the inflammation occurs
repeatedly over a long time period.
People who are of particular concern
with respect to ozone exposures include
children and adults who are active
outdoors. Those people particularly
susceptible to ozone effects are people
with respiratory disease (e.g., asthma),
people with unusual sensitivity to
ozone, and children.
There has been new research that
suggests additional serious health
effects beyond those that had been
known when the 1996 ozone CD was
published. Since then, over 1,700 new
ozone-related health and welfare studies
have been published in peer-reviewed
journals.122 Many of these studies have
investigated the impact of ozone
exposure on such health effects as
changes in lung structure and
biochemistry, inflammation of the
lungs, exacerbation and causation of
asthma, respiratory illness-related
school absence, hospital and emergency
room visits for asthma and other
respiratory causes, and premature
Paper, EPA–452/R–96–007. This document is
available in Docket EPA–HQ–OAR–2005–0036.
121 U.S. EPA (2005) Air Quality Criteria for Ozone
and Related Photochemical Oxidants (Second
External Review Draft). This document is available
in Docket EPA–HQ–OAR–2005–0036.
122 New Ozone Health and Environmental Effects
References, Published Since Completion of the
Previous Ozone AQCD, National Center for
Environmental Assessment, Office of Research and
Development, U.S. Environmental Protection
Agency, Research Triangle Park, NC 27711 (7/2002).
This document is available in Docket EPA–HQ–
OAR–2005–0036.
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mortality. EPA is currently in the
process of evaluating these and other
studies as part of the ongoing review of
the air quality criteria document and
NAAQS for ozone. Key new health
information falls into four general areas:
development of new-onset asthma,
hospital admissions for young children,
school absence rate, and premature
mortality.
Aggravation of existing asthma
resulting from short-term ambient ozone
exposure was reported prior to the 1997
NAAQS standard and has been observed
in studies published subsequently.123 124
In addition, a relationship between
long-term ambient ozone concentrations
and the incidence of new-onset asthma
in adult males (but not in females) was
reported by McDonnell et al. (1999).125
Subsequently, an additional study
suggests that incidence of new
diagnoses of asthma in children is
associated with heavy exercise in
communities with high concentrations
(i.e., mean 8-hour concentration of 59.6
parts per billion (ppb) or greater) of
ozone.126 This relationship was
documented in children who played 3
or more sports and thus spent more time
outdoors. It was not documented in
those children who played one or two
sports.
Previous studies have shown
relationships between ozone and
hospital admissions in the general
population. A study in Toronto reported
a significant relationship between
1-hour maximum ozone concentrations
and respiratory hospital admissions in
children under the age of two.127 Given
the relative vulnerability of children in
this age category, there is particular
concern about these findings.
Increased rates of illness-related
school absenteeism have been
associated with 1-hour daily maximum
123 Thurston, G.D.; Lippman, M.L.; Scott, M.B.;
Fine, J.M. (1997) Summertime Haze Air Pollution
and Children with Asthma. American Journal of
Respiratory Critical Care Medicine 155: 654–660.
124 Ostro, B.; Lipsett, M.; Mann, J.; BraxtonOwens, H.; White, M. (2001) Air pollution and
exacerbation of asthma in African-American
children in Los Angeles. Epidemiology 12(2): 200–
208.
125 McDonnell, W.F.; Abbey, D.E.; Nishino, N.;
Lebowitz, M.D. (1999) ‘‘Long-term ambient ozone
concentration and the incidence of asthma in
nonsmoking adults: the AHSMOG study.’’
Environmental Research 80(2 Pt 1): 110–121.
126 McConnell, R.; Berhane, K.; Gilliland, F.;
London, S.J.; Islam, T.; Gauderman, W.J.; Avol, E.;
Margolis, H.G.; Peters, J.M. (2002) Asthma in
exercising children exposed to ozone: a cohort
study. Lancet 359: 386–391.
127 Burnett, R.T.; Smith-Doiron, M.; Stieb, D.;
Raizenne, M.E.; Brook, J.R.; Dales, R.E.; Leech, J.A.;
Cakmak, S.; Krewski, D. (2001) Association between
ozone and hospitalization for acute respiratory
diseases in children less than 2 years of age. Am.
J. Epidemiol. 153: 444–452.
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and 8-hour average ozone
concentrations in studies conducted in
Nevada 128 in kindergarten to 6th grade
and in Southern California in grades
four through six.129 These studies
suggest that higher ambient ozone levels
may result in increased school
absenteeism.
The air pollutant most clearly
associated with premature mortality is
PM, with many studies reporting such
an association. However, recent
analyses provide evidence that short
term ozone exposure is associated with
increased premature mortality. Bell et
al. (2004) published new analyses of the
95 cities in the National Morbidity,
Mortality, and Air Pollution Study
(NMMAPS) data sets, showing
associations between daily mortality
and the previous week’s ozone
concentrations which were robust to
adjustment for particulate matter,
weather, seasonality, and long-term
trends.130 Although earlier analyses
undertaken as part of the NMMAPS did
not report an effect of ozone on total
mortality across the full year, in those
earlier studies the NMMAPS
investigators did observe an effect after
limiting the analysis to summer, when
ozone levels are highest.131 132 Another
recent study from 23 cities throughout
Europe (APHEA2) also found an
association between ambient ozone and
daily mortality.133 Similarly, other
studies have shown associations
128 Chen, L.; Jennison, B.L.; Yang, W.; Omaye,
S.T. (2000) Elementary school absenteeism and air
pollution. Inhalation Toxicol. 12: 997–1016.
129 Gilliland, F.D.; Berhane, K.; Rappaport, E.B.;
Thomas, D.C.; Avol, E.; Gauderman, W.J.; London,
S.J.; Margolis, H.G.; McConnell, R.; Islam, K.T.;
Peters, J.M. (2001) The effects of ambient air
pollution on school absenteeism due to respiratory
illnesses. Epidemiology 12:43–54.
130 Bell, M.L.; McDermott, A.; Zeger, S.L.; Samet,
J.M.; Dominici, F. Ozone and short-term mortality
in 95 U.S. urban communities, 1987–2000. JAMA
292(19): 2372–2378.
131 Samet, J.M.; Zeger, S.L.; Dominici, F.;
Curriero, F.; Coursac, I.; Dockery, D.W.; Schwartz,
J.; Zanobetti, A. (2000) The National Morbidity,
Mortality and Air Pollution Study: Part II:
Morbidity, Mortality and Air Pollution in the
United States. Research Report No. 94, Part II.
Health Effects Institute, Cambridge, MA, June 2000.
This document is available in Docket EPA–HQ–
OAR–2005–0036.
132 Samet, J.M.; Zeger, S.L.; Dominici, F.;
Curriero, F.; Coursac, I.; Zeger, S. (2000) Fine
Particulate Air Pollution and Mortality in 20 U.S.
Cities, 1987–1994. The New England Journal of
Medicine 343(24): 1742–1749.
133 Gryparis, A.; Forsberg, B.; Katsouyanni, K.;
Analitis, A.; Touloumi, G.; Schwartz, J.; Samoli, E.;
Medina, S.; Anderson, H.R.; Niciu, E.M.;
Wichmann, H.E.; Kriz, B.; Kosnik, M.; Skorkovsky,
J.; Vonk, J.M.; Dortbudak, Z. (2004) Acute effects of
ozone on mortality from the ‘‘Air Pollution and
Health: A European Approach’’ project. Am. J.
Respir. Crit. Care Med. 170: 1080–1087.
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between ozone and mortality.134 135
Specifically, Toulomi et al. (1997) found
that 1-hour maximum ozone levels were
associated with daily numbers of deaths
in four cities (London, Athens,
Barcelona, and Paris), and a
quantitatively similar effect was found
in a group of four additional cities
(Amsterdam, Basel, Geneva, and
Zurich).
In all, the new studies that have
become available since the 8-hour ozone
standard was adopted in 1997 continue
to demonstrate the harmful effects of
ozone on public health, and the need to
attain and maintain the ozone NAAQS.
3. Current and Projected 8-Hour Ozone
Levels
Currently, ozone concentrations
exceeding the level of the 8-hour ozone
NAAQS occur over wide geographic
areas, including most of the nation’s
major population centers.136 As of
September 2005 there are approximately
159 million people living in 126 areas
designated as not in attainment with the
8-hour ozone NAAQS. There are 474
full or partial counties that make up the
8-hour ozone nonattainment areas.
EPA has already adopted many
emission control programs that are
expected to reduce ambient ozone
levels. These control programs include
the Clean Air Interstate Rule (70 FR
25162, May 12, 2005), as well as many
mobile source rules (many of which are
described in section V.D). As a result of
these programs, the number of areas that
fail to achieve the 8-hour ozone NAAQS
is expected to decrease.
Based on the recent ozone modeling
performed for the CAIR analysis 137,
barring additional local ozone precursor
controls, we estimate 37 Eastern
counties (where 24 million people are
projected to live) will exceed the 8-hour
ozone NAAQS in 2010. An additional
148 Eastern counties (where 61 million
people are projected to live) are
expected to be within 10 percent of
violating the 8-hour ozone NAAQS in
2010.
States with 8-hour ozone
nonattainment areas will be required to
134 Thurston, G.D.; Ito, K. (2001) Epidemiological
studies of acute ozone exposures and mortality. J.
Exposure Anal. Environ. Epidemiol. 11: 286–294.
135 Touloumi, G.; Katsouyanni, K.; Zmirou, D.;
Schwartz, J.; Spix, C.; Ponce de Leon, A.; Tobias,
A.; Quennel, P.; Rabczenko, D.; Bacharova, L.;
Bisanti, L.; Vonk, J.M.; Ponka, A. (1997) Short-term
effects of ambient oxidant exposure on mortality: A
combined analysis within the APHEA project. Am.
J. Epidemiol. 146: 177–185.
136 A map of the 8-hour ozone nonattainment
areas is included in the RIA for this proposed rule.
137 Technical Support Document for the Final
Clean Air Interstate Rule Air Quality Modeling.
This document is available in Docket EPA–HQ–
OAR–2005–0036.
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take action to bring those areas into
compliance in the future. Based on the
final rule designating and classifying 8hour ozone nonattainment areas (69 FR
23951, April 30, 2004), most 8-hour
ozone nonattainment areas will be
required to attain the 8-hour ozone
NAAQS in the 2007 to 2013 time frame
and then be required to maintain the 8hour ozone NAAQS thereafter.138 We
also expect many of the 8-hour ozone
nonattainment areas to adopt additional
emission reduction programs, but we
are unable to quantify or rely upon
future reductions from additional state
and local programs that have not yet
been adopted. The expected ozone
inventory reductions from the standards
proposed in this action may be useful to
states in attaining or maintaining the 8hour ozone NAAQS.
A metamodeling tool developed at
EPA, the ozone response surface
metamodel, was used to estimate the
effects of the proposed emission
reductions. The ozone response surface
metamodel was created using multiple
runs of the Comprehensive Air Quality
Model with Extensions (CAMx). Base
and proposed control CAMx
metamodeling was completed for two
future years (2020, 2030) over a
modeling domain that includes all or
part of 37 Eastern U.S. states. For more
information on the response surface
metamodel, please see the RIA for this
proposal or the Air Quality Modeling
Technical Support Document (TSD).
We have made estimates using the
ozone response surface metamodel to
illustrate the types of change in future
ozone levels that we would expect to
result from this proposed rule, as
described in Chapter 3 of the draft RIA.
The proposed gas can controls are
projected to result in a very small net
improvement in future ozone, after
weighting for population. Although the
net future ozone improvement is small,
some VOC-limited areas in the Eastern
U.S. are projected to have non-negligible
improvements in projected 8-hour
ozone design values due to the proposed
gas can controls. As stated in Section
VII.E.3, we view these improvements as
useful in meeting the 8-hour ozone
NAAQS. These net ozone improvements
are in addition to reductions in levels of
benzene due to the proposed gas can
controls.
D. Particulate Matter
The cold temperature vehicle controls
proposed here will result in reductions
of primary PM being emitted by
138 The Los Angeles South Coast Air Basin 8-hour
ozone nonattainment area will have to attain before
June 15, 2021.
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vehicles. In addition, both the proposed
vehicle controls and the proposed gas
can controls will reduce VOCs that react
in the atmosphere to form secondary
PM2.5, namely organic carbonaceous
PM2.5.
1. Background
Particulate matter (PM) represents a
broad class of chemically and physically
diverse substances. It can be principally
characterized as discrete particles that
exist in the condensed (liquid or solid)
phase spanning several orders of
magnitude in size. PM is further
described by breaking it down into size
fractions. PM10 refers to particles with
an aerodynamic diameter less than or
equal to a nominal 10 micrometers (µm).
PM2.5 refers to fine particles, those
particles with an aerodynamic diameter
less than or equal to a nominal 2.5 µm.
Coarse fraction particles refer to those
particles with an aerodynamic diameter
less than or equal to a nominal 10 µm.
Inhalable (or ‘‘thoracic’’) coarse particles
refer to those particles with an
aerodynamic diameter greater than 2.5
µm but less than or equal to 10 µm.
Ultrafine PM refers to particles with
diameters of less than 100 nanometers
(0.1 µm). Larger particles (>10 µm) tend
to be removed by the respiratory
clearance mechanisms, whereas smaller
particles are deposited deeper in the
lungs. Ambient fine particles are a
complex mixture including sulfates,
nitrates, chlorides, organic
carbonaceous material, elemental
carbon, geological material, and metals.
Fine particles can remain in the
atmosphere for days to weeks and travel
through the atmosphere hundreds to
thousands of kilometers, while coarse
particles generally tend to deposit to the
earth within minutes to hours and
within tens of kilometers from the
emission source.
EPA has NAAQS for both PM2.5 and
PM10. Both the PM2.5 and PM10 NAAQS
consist of a short-term (24-hour) and a
long-term (annual) standard. The 24hour PM2.5 NAAQS is set at a level of
65 µg/m3 based on the 98th percentile
concentration averaged over three years.
The annual PM2.5 NAAQS specifies an
expected annual arithmetic mean not to
exceed 15 µg/m3 averaged over three
years. The 24-hour PM10 NAAQS is set
at a level of 150 µg/m3 not to be
exceeded more than once per year. The
annual PM10 NAAQS specifies an
expected annual arithmetic mean not to
exceed 50 µg/m3.
EPA has recently proposed to amend
the PM NAAQS.139 The proposal
139 U.S. EPA, National Ambient Air Quality
Standards for Particulate Matter (71 FR 2620, Jan.
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15829
includes lowering the level of the
primary 24-hour fine particle standard
from the current level of 65 micrograms
per cubic meter (µg/m3) to 35 µg/m3,
retaining the level of the annual fine
standard at 15 µg/m3, and setting a new
primary 24-hour standard for certain
inhalable coarse particles (the indicator
is qualified so as to include any ambient
mix of PM10–2.5 that is dominated by
resuspended dust from high-density
traffic on paved roads and PM generated
by industrial and construction sources,
and excludes any ambient mix of
PM10–2.5 dominated by rural windblown
dust and soils and PM generated by
agricultural and mining sources) at 70
µg/m3. The Agency is also requesting
comment on various other standards for
fine and inhalable coarse PM (71 FR
2620, Jan. 17, 2006).
2. Health Effects of PM
Scientific studies show ambient PM is
associated with a series of adverse
health effects. These health effects are
discussed in detail in the 1997 PM
criteria document, the recent 2004 EPA
Criteria Document for PM as well as the
2005 PM Staff Paper.140 141 142 Further
discussion of health effects associated
with PM can also be found in the draft
RIA for this proposal.
As described in the documents listed
above, health effects associated with
short-term variation (e.g. hours to days)
in ambient PM2.5 include premature
mortality, hospital admissions, heart
and lung diseases, increased cough,
lower-respiratory symptoms,
decrements in lung function and
changes in heart rate rhythm and other
cardiac effects. Studies examining
populations exposed to different levels
of air pollution over a number of years,
including the Harvard Six Cities Study
and the American Cancer Society Study,
show associations between long-term
exposure to ambient PM2.5 and
premature mortality, including deaths
attributed to cardiovascular changes and
lung cancer.
17, 2006). This document is also available on the
web at: https://www.epa.gov/air/particlepollution/
actions.html
140 U.S.EPA (1996) Air Quality Criteria for
Particulate Matter, EPA 600–P–95–001aF, EPA 600–
P–95–001bF. This document is available in Docket
EPA–HQ–OAR–2005–0036.
141 U.S. EPA (2004) Air Quality Criteria for
Particulate Matter (Oct 2004), Volume I Document
No. EPA600/P–99/002aF and Volume II Document
No. EPA600/P–99/002bF. This document is
available in Docket EPA–HQ–OAR–2005–0036.
142 U.S. EPA (2005) Review of the National
Ambient Air Quality Standard for Particulate
Matter: Policy Assessment of Scientific and
Technical Information, OAQPS Staff Paper. EPA–
452/R–05–005. This document is available in
Docket EPA–HQ–OAR–2005–0036.
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Recently, several studies have
highlighted the adverse effects of PM
specifically from mobile sources.143 144
Studies have also focused on health
effects due to PM exposures on or near
roadways.145 Although these studies
include all air pollution sources,
including both spark-ignition (gasoline)
and diesel powered vehicles, they
indicate that exposure to PM emissions
near roadways, thus dominated by
mobile sources, are associated with
health effects. The proposed vehicle
controls may help to reduce exposures
to mobile source related PM2.5.
Additional information on near roadway
health effects can be found in Section III
of this preamble.
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3. Current and Projected PM2.5 Levels
EPA has recently finalized PM2.5
nonattainment designations (70 FR 943,
Jan 5. 2005).146 As can be seen from the
designations, ambient PM2.5 levels
exceeding the level of the PM2.5 NAAQS
are widespread throughout the country.
There are approximately 88 million
people living in 39 areas (which include
all or part of 208 counties) designated as
not in attainment with the PM2.5
NAAQS.
EPA has already adopted many
emission control programs that are
expected to reduce ambient PM levels.
These rules include the Clean Air
Interstate Rule (70 FR 25162, May 12,
2005), as well as many mobile source
rules. Section V.D details many of these
mobile source rules.147 As a result of
these programs, the number of areas that
fail to achieve the 1997 PM2.5 NAAQS
is expected to decrease. Based on
modeling performed for the CAIR
analysis, we estimate that 28 Eastern
counties (where 19 million people are
143 Laden, F.; Neas, L.M.; Dockery, D.W.;
Schwartz, J. (2000) Association of Fine Particulate
Matter from Different Sources with Daily Mortality
in Six U.S. Cities. Environmental Health
Perspectives 108: 941–947.
144 Janssen, N.A.H.; Schwartz, J.; Zanobetti, A.;
Suh, H.H. (2002) Air Conditioning and SourceSpecific Particles as Modifiers of the Effect of PM10
on Hospital Admissions for Heart and Lung Disease.
Environmental Health Perspectives 110: 43–49.
145 Riekider, M.; Cascio, W.E.; Griggs, T.R.;
Herbst, M.C.; Bromberg, P.A.; Neas, L.; Williams,
R.W.; Devlin, R.B. (2003) Particulate Matter
Exposures in Cars is Associated with
Cardiovascular Effects in Healthy Young Men. Am.
J. Respir. Crit. Care Med. 169: 934–940.
146 US EPA, Air Quality Designations and
Classifications for the Fine Particles (PM2.5)
National Ambient Air Quality Standards, December
17, 2004. (70 FR 943, Jan 5, 2005) This document
is also available on the web at: https://www.epa.gov/
pmdesignations/.
147 The Clean Air Interstate Rule (CAIR) will
reduce emissions of SO2 and NOX from power
plants in the Eastern 37 states, reducing interstate
transport of nitrogen oxides and sulfur dioxide and
helping cities and states in the East meet the ozone
and PM NAAQS. (70 FR 25162) (May 12, 2005).
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projected to live) will exceed the PM2.5
standard in 2010.148 In addition, 56
Eastern counties (where 24 million
people are projected to live) are
expected to be within 10 percent of
violating the PM2.5 in 2010.
While the final implementation
process for bringing the nation’s air into
attainment with the 1997 PM2.5 NAAQS
is still being completed in a separate
rulemaking action, we expect that most
areas will need to attain the 1997 PM2.5
NAAQS in the 2009 to 2014 time frame,
and then be required to maintain the
NAAQS thereafter. The expected PM
and VOC inventory reductions from the
standards proposed in this action will
be useful to states in attaining or
maintaining the PM2.5 NAAQS.
4. Current PM10 Levels
Air quality monitoring data indicates
that as of September 2005
approximately 29 million people live in
55 designated PM10 nonattainment
areas, which include all or part of 54
counties. The RIA for this proposed rule
lists the PM10 nonattainment areas and
their populations.
Based on section 188 of the Act, we
expect that most areas will attain the
PM10 NAAQS no later than December
31, 2006, depending on an area’s
classification and other factors, and then
be required to maintain the PM10
NAAQS thereafter. The expected PM
and VOC inventory reductions from the
standards proposed in this action could
be useful to states in maintaining the
PM10 NAAQS.149
E. Other Environmental Effects
1. Visibility
a. Background
Visibility can be defined as the degree
to which the atmosphere is transparent
to visible light.150 Visibility is important
148 Technical Support Document for the Final
Clean Air Interstate Rule Air Quality Modeling.
This document is available in Docket EPA–HQ–
OAR–2005–0036.
149 As mentioned above, the EPA has recently
proposed to amend the PM NAAQS, by establishing
a new indicator for certain inhalable coarse
particles, and a new primary 24-hour standard for
coarse particles described by that indicator. EPA
also proposed to revoke the current 24-hour PM10
standard in all areas of the country except in those
areas with a population of at least 100,000 people
and which contain at least one monitor violating
the 24-hour PM10 standard, based on the most
recent 3 years of air quality data. In addition, EPA
proposed to revoke upon promulgation of this rule
the current annual PM10 standard if EPA finalizes
the proposed primary standard for PM10¥2.5 (71 FR
2620, Jan. 17, 2006).
150 National Research Council, 1993. Protecting
Visibility in National Parks and Wilderness Areas.
National Academy of Sciences Committee on Haze
in National Parks and Wilderness Areas. National
Academy Press, Washington, DC. This document is
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because it has direct significance to
people’s enjoyment of daily activities in
all parts of the country. Individuals
value good visibility for the well-being
it provides them directly, where they
live and work, and in places where they
enjoy recreational opportunities.
Visibility is also highly valued in
significant natural areas such as
national parks and wilderness areas,
because of the special emphasis given to
protecting these lands now and for
future generations. For more
information on visibility see the recent
2004 EPA Criteria Document for PM as
well as the 2005 PM Staff Paper.151 152
To address the welfare effects of PM
on visibility, EPA set secondary PM2.5
standards in 1997 which would act in
conjunction with the establishment of a
regional haze program. EPA concluded
that PM2.5 causes adverse effects on
visibility in various locations,
depending on PM concentrations and
factors such as chemical composition
and average relative humidity and the
secondary (welfare-based) PM2.5
NAAQS was established as equal to the
suite of primary (health-based) NAAQS
(62 FR 38669, July 18, 1997).
Furthermore, Section 169 of the Act
provides additional authorities to
remedy existing visibility impairment
and prevent future visibility impairment
in the 156 national parks, forests and
wilderness areas categorized as
mandatory Federal class I areas (62 FR
38680–81, July 18, 1997).153 In July
1999 the regional haze rule (64 FR
35714) was put in place to protect the
visibility in mandatory Federal class I
areas. Visibility can be said to be
impaired in both PM2.5 nonattainment
areas and mandatory Federal class I
areas.154
available in Docket EPA–HQ–OAR–2005–0036.
This book can be viewed on the National Academy
Press Website at https://www.nap.edu/books/
0309048443/html/.
151 U.S. EPA (2004) Air Quality Criteria for
Particulate Matter (Oct 2004), Volume I Document
No. EPA600/P–99/002aF and Volume II Document
No. EPA600/P–99/002bF. This document is
available in Docket EPA–HQ–OAR–2005–0036.
152 U.S. EPA (2005) Review of the National
Ambient Air Quality Standard for Particulate
Matter: Policy Assessment of Scientific and
Technical Information, OAQPS Staff Paper. EPA–
452/R–05–005. This document is available in
Docket EPA–HQ–OAR–2005–0036.
153 These areas are defined in section 162 of the
Act as those national parks exceeding 6,000 acres,
wilderness areas and memorial parks exceeding
5,000 acres, and all international parks which were
in existence on August 7, 1977.
154 As mentioned above, the EPA has recently
proposed to amend the PM NAAQS (71 FR 2620,
Jan. 17, 2006). The proposal would set the
secondary NAAQS equal to the primary standards
for both PM2.5 and PM10¥2.5. EPA also is taking
comment on whether to set a separate PM2.5
standard, designed to address visibility (principally
in urban areas), on potential levels for that standard
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2. Plant Damage From Ozone
Ozone contributes to many
Data showing PM2.5 nonattainment
environmental effects, with damage to
areas, and visibility levels above
plants and ecosystems being of most
background at the Mandatory Class I
concern. Plant damage affects crop
Federal Areas demonstrate that
yields, forestry production, and
unacceptable visibility impairment is
ornamentals. The adverse effect of
experienced throughout the U.S., in
ozone on forests and other natural
multi-state regions, urban areas, and
vegetation can in turn cause damage to
remote mandatory Federal class I
areas.155 156 The mandatory federal class associated ecosystems, with additional
I areas are listed in Chapter 3 of the draft resulting economic losses. Prolonged
ozone concentrations of 100 ppb can be
RIA for this action. The areas that have
phytotoxic to a large number of plant
design values above the PM2.5 NAAQS
species, and can produce acute injury
are also listed in Chapter 3 of the draft
and reduced crop yield and biomass
RIA for this action.
production. Ozone concentrations
c. Future Visibility Impairment
within the range of 50 to 100 ppb have
the potential over a longer duration to
Recent modeling for the Clean Air
create chronic stress on vegetation that
Interstate Rule (CAIR) was used to
can result in reduced plant growth and
project visibility conditions in
yield, shifts in competitive advantages
mandatory Federal class I areas across
in mixed populations, decreased vigor,
the country in 2015. The results for the
and injury. Ozone effects on vegetation
mandatory Federal Class I areas suggest
are presented in more detail in the 1996
that these areas are predicted to
Criteria Document and the 2005 draft
continue to have annual average
deciview levels above background in the Criteria Document.
future.157 Modeling done for the CAIR
3. Atmospheric Deposition
also projected PM2.5 levels in the
Wet and dry deposition of ambient
Eastern U.S. in 2010. These projections
particulate matter delivers a complex
include all sources of PM2.5, including
mixture of metals (e.g., mercury, zinc,
the engines covered in this proposal,
lead, nickel, aluminum, cadmium),
and suggest that PM2.5 levels above the
organic compounds (e.g., POM, dioxins,
1997 NAAQS will persist into the
furans) and inorganic compounds (e.g.,
future.158
nitrate, sulfate) to terrestrial and aquatic
The vehicles that would be subject to
ecosystems. EPA’s Great Waters
the proposed standards contribute to
Program has identified 15 pollutants
visibility concerns in these areas
whose deposition to water bodies has
through both their primary PM
contributed to the overall contamination
emissions and their VOC emissions,
loadings to these Great Waters. These 15
which contribute to the formation of
compounds include several heavy
secondary PM2.5. The gas cans that
metals and a group known as polycyclic
would be subject to the proposed
organic matter (POM). Within POM are
standards also contribute to visibility
the polycyclic aromatic hydrocarbons
concerns through their VOC emissions.
(PAHs). PAHs in the environment may
Reductions in these direct PM and VOC be present in the gas or particle phase,
emissions will help to improve visibility although the bulk will be adsorbed onto
across the nation, including mandatory
airborne particulate matter. In most
Federal class I areas.
cases, human-made sources of PAHs
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b. Current Visibility Impairment
within a range of 20 to 30 µg/m3, and on averaging
times for the standard within a range of four to eight
daylight hours.
155 US EPA, Air Quality Designations and
Classifications for the Fine Particles (PM2.5)
National Ambient Air Quality Standards, December
17, 2004. (70 FR 943, Jan 5. 2005) This document
is also available on the web at: https://www.epa.gov/
pmdesignations/.
156 US EPA. Regional Haze Regulations, July 1,
1999. (64 FR 35714, July 1, 1999).
157 The deciview metric describes perceived
visual changes in a linear fashion over its entire
range, analogous to the decibel scale for sound. A
deciview of 0 represents pristine conditions. The
higher the deciview value, the worse the visibility,
and an improvement in visibility is a decrease in
deciview value.
158 EPA recently proposed to revise the current
secondary PM NAAQS standards by making them
identical to the suite of proposed primary standards
for fine and coarse particles (71 FR 2620, Jan. 17,
2006).
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account for the majority of PAHs
released to the environment. The PAHs
are usually the POMs of concern as
many PAHs are probable human
carcinogens.159 For some watersheds,
atmospheric deposition represents a
significant input to the total surface
water PAH burden.160 161 Emissions
159 Deposition of Air Pollutants to the Great
Waters-Third Report to Congress, Office of Air
Quality Planning and Standards, June 2000,
EPA453–R–00–005. This document is available in
Docket EPA–HQ–OAR–2005–0036.
160 Simcik, M.F.; Eisenrich, S.J.; Golden, K.A.;
Liu, S.; Lipiatou, E.; Swackhamer, D.L.; and Long,
D.T. (1996) Atmospheric Loading of Polycyclic
Aromatic Hydrocarbons to Lake Michigan as
Recorded in the Sediments. Environ. Sci. Technol.
30:3039–3046.
161 Simcik, M.F.; Eisenrich, S.J.; and Lioy, P.J.
(1999) Source Apportionment and Source/Sink
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from mobile sources have been found to
account for a percentage of the
atmospheric deposition of PAHs. For
instance, recent studies have identified
gasoline and diesel vehicles as the major
contributors in the atmospheric
deposition of PAHs to Chesapeake Bay,
Massachusetts Bay and Casco Bay.162 163
The vehicle controls being proposed
may help to reduce deposition of heavy
metals and POM.
4. Materials Damage and Soiling
The deposition of airborne particles
can also reduce the aesthetic appeal of
buildings and culturally important
articles through soiling, and can
contribute directly (or in conjunction
with other pollutants) to structural
damage by means of corrosion or
erosion.164 Particles affect materials
principally by promoting and
accelerating the corrosion of metals, by
degrading paints, and by deteriorating
building materials such as concrete and
limestone. Particles contribute to these
effects because of their electrolytic,
hygroscopic, and acidic properties, and
their ability to sorb corrosive gases
(principally sulfur dioxide). The rate of
metal corrosion depends on a number of
factors, including the deposition rate
and nature of the pollutant; the
influence of the metal protective
corrosion film; the amount of moisture
present; variability in the
electrochemical reactions; the presence
and concentration of other surface
electrolytes; and the orientation of the
metal surface.
V. What Are Mobile Source Emissions
Over Time and How Would This
Proposal Reduce Emissions, Exposure
and Associated Health Effects?
A. Mobile Source Contribution to Air
Toxics Emissions
In 1999, based on the National
Emissions Inventory (NEI), mobile
sources accounted for 44% of total
Relationships of PAHs in the Coastal Atmosphere
of Chicago and Lake Michigan. Atmospheric
Environment 33: 5071–5079.
162 Dickhut, R.M.; Canuel, E.A.; Gustafson, K.E.;
Liu, K.; Arzayus, K.M.; Walker, S.E.; Edgecombe, G.;
Gaylor, M.O.; and McDonald, E.H. (2000)
Automotive Sources of Carcinogenic Polycyclic
Aromatic Hydrocarbons Associated with Particulate
Matter in the Chesapeake Bay Region. Environ. Sci.
Technol. 34: 4635–4640.
163 Golomb, D.; Barry, E.; Fisher, G.;
Varanusupakul, P.; Koleda, M.; amd Rooney, T.
(2001) Atmospheric Deposition of Polycyclic
Aromatic Hydrocarbons near New England Coastal
Waters. Atmospheric Environment 35: 6245–6258.
164 U.S. EPA (2005) Review of the National
Ambient Air Quality Standards for Particulate
Matter: Policy Assessment of Scientific and
Technical Information, OAQPS Staff Paper. This
document is available in Docket EPA–HQ–OAR–
2005–0036.
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emissions of 188 hazardous air
pollutants (on the Clean Air Act section
112(b) list of hazardous air pollutants).
Diesel particulate matter (PM) is not
included in this list of 188 pollutants.
Sixty-five percent of the mobile source
tons in this inventory were attributable
to highway mobile sources, and the
remainder to nonroad sources.
Furthermore, over 90% of mobile source
emissions of air toxics (not including
diesel PM) are attributable to gasoline
vehicles and equipment.
Recently, EPA projected trends in air
toxic emissions (not including diesel
PM) to 2020, using the 1999 National
Emissions Inventory (NEI) as a
baseline.165 Overall, air toxic emissions
are projected to decrease from 5,030,000
tons in 1999 to 4,010,000 tons in 2020,
as a result of emission controls on
major, area, and mobile sources. In the
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165 Strum, M., R. Cook, J. Thurman, D. Ensley, A.
Pope, T. Palma, R. Mason, H. Michaels, and S.
Shedd. 2005. Projection of Hazardous Air Pollutant
Emissions to Future Years. Science of the Total
Environment, in press.
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absence of Clean Air Act emission
controls currently in place, EPA
estimates air toxic emissions would
total 11,590,000 tons in 2020.
Figure V.A–1 depicts the
contributions of source categories to air
toxic emissions between 1990 and
2020.166 As indicated in Figure V.A–1,
mobile source air toxic emissions will
be reduced 60% between 1999 and
2020, from 2.2 million to 880,000 tons.
This reduction will occur despite a
projected 57% increase in vehicle miles
traveled, and a projected 63% increase
in nonroad activity, based on units of
work called horsepower-hours. It should
be noted, however, that EPA anticipates
mobile source air toxic emissions will
begin to increase after 2020, from about
880,000 tons in 2020 to 920,000 tons in
166 It should be noted that after 2010, stationary
source emissions are based only on economic
growth, and do not account for reductions from
ongoing toxics programs such as the urban air
toxics program, residual risk standards and area
source program, which are expected to further
reduce toxics.
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2030. This is because, after 2020,
reductions from control programs will
be outpaced by increases in activity.
In 1999, 29% of air toxic emissions
were from highway vehicles and 15%
from nonroad equipment. Moreover,
54% of air toxic emissions from
highway vehicles were emitted by lightduty gasoline vehicles (LDGVs) and
37% by light-duty trucks (LDGTs) (see
Table V.A–1). EPA projects that in 2020,
only 27% of highway vehicle toxic
emissions will be from LDGVs and 63%
will be from LDGTs. Air toxic emissions
from nonroad equipment are dominated
by lawn and garden equipment,
recreational equipment, and pleasure
craft, which collectively accounted for
almost 80% of nonroad toxic emissions
in 1999 and 2020 (see Table V.A–2).
Figure V.A–1Contribution of Source
Categories to Air Toxic Emissions, 1990
to 2020 (not including diesel particulate
matter). Note: Dashed line represents
projected emissions without Clean Air
Act controls.
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If diesel PM emissions were added to
the mobile source total, mobile sources
would account for 48% of a total
5,398,000 tons in 1999. Figure V.A.–2
summarizes the trend in diesel PM
between 1999 and 2020, by source
category. Diesel PM emissions will be
reduced from 368,000 tons in 1999 to
114,000 tons in 2020, a decrease of 70%.
As controls on highway diesel engines
and nonroad diesel engines phase in,
diesel-powered locomotives and
commercial marine vessels increase
from 11% of the inventory in 1999 to
27% in 2020.
Subsequent to the development of
these projected inventories for mobile
source air toxics, a number of inventory
revisions have occurred. Data EPA has
collected indicate that the MOBILE6.2
emission factor model is under
predicting hydrocarbon emissions
(including air toxics) and PM emissions
at lower temperatures, from light-duty
vehicles meeting National Low
Emission Vehicle (NLEV) and Tier 2
tailpipe standards. The inventories
presented in sections V.B, V.C., and V.E.
reflect these enhancements.
TABLE V.A–1.—PERCENT CONTRIBUTION OF VEHICLE CLASSES TO HIGHWAY VEHICLE AIR TOXIC EMISSIONS, 1999 TO
2020
[Not including diesel particulate matter]
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Light-Duty Gasoline Vehicles ...................................................................
Light-Duty Gasoline Trucks .....................................................................
Heavy-Duty Gasoline Vehicles ................................................................
Heavy-Duty Diesel Vehicles ....................................................................
Other (motorcycles and light-duty diesel vehicles and trucks) ................
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(%)
54
37
6
3
1
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2010
(%)
41
49
5
4
1
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2015
(%)
37
53
4
4
1
29MRP2
2020
(%)
31
59
4
4
2
27
63
3
5
2
EP29MR06.001
1999
(%)
Vehicle
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TABLE V.A–2.—CONTRIBUTION OF EQUIPMENT TYPES TO NONROAD AIR TOXIC EMISSIONS, 1999 TO 2020
1999
(%)
Equipment type
Lawn and Garden ....................................................................................
Pleasure Craft ..........................................................................................
Recreational .............................................................................................
All Others .................................................................................................
B. VOC Emissions From Mobile Sources
26
34
19
21
obtained from the National Emissions
Inventory, and the 2010 and later year
estimates were obtained from the
inventories developed for the Clean Air
Interstate Air Quality Rule (CAIR). The
table provides emissions for nonroad
equipment such as commercial marine
vessels, locomotives, aircraft, lawn and
2010
(%)
18
27
38
17
2015
(%)
17
25
40
18
2020
(%)
21
25
35
19
25
25
29
21
garden equipment, recreational vehicles
and boats, industrial equipment, and
construction equipment. The estimates
for highway vehicle classes were
developed for this rule. The estimates
for light-duty gasoline vehicles reflect
revised estimates of hydrocarbon
emissions at low temperatures.
TABLE V.B–1.—48-STATE VOC EMISSIONS (TONS) FROM KEY MOBILE SOURCE SECTORS IN 1999, 2010, 2015, AND
2020
[Without this proposed rule]
Category
1999
Light Duty Gasoline Vehicles and Trucks .......................................................
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2010
2015
2020
4,873,000
2,896,000
2,566,000
2,486,000
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Table V.B–1 presents 48-State VOC
emissions from key mobile source
sectors in 1999, 2010, 2015, and 2020,
not including the effects of this
proposed rule. The 1999 inventory
estimates for nonroad equipment were
2007
(%)
Federal Register / Vol. 71, No. 60 / Wednesday, March 29, 2006 / Proposed Rules
15835
TABLE V.B–1.—48-STATE VOC EMISSIONS (TONS) FROM KEY MOBILE SOURCE SECTORS IN 1999, 2010, 2015, AND
2020—Continued
[Without this proposed rule]
Category
1999
Heavy Duty and Other Highway Vehicles .......................................................
Nonroad Equipment .........................................................................................
VOC emissions from highway
vehicles are about twice those from
nonroad equipment in 1999. Emissions
from both highway vehicles and
nonroad equipment decline
substantially between 1999 and 2020 as
a result of EPA control programs that are
already adopted. The VOC emission
reductions associated with this
proposed rule are presented in section
V.E, below.
2010
2015
2020
672,000
2,785,000
255,000
1,739,000
212,000
1,500,000
200,000
1,387,000
C. PM Emissions From Mobile Sources
Table V.C–1 presents 48-State
PM2.5 167 emissions from key mobile
source sectors in 1999, 2010, 2015, and
2020, not including the effects of this
proposed rule. The estimates in Table
V.C–1 come from the same sources as
the VOC estimates in section V.B. EPA
is considering revisions to estimates of
the PM emissions inventory for motor
vehicles. Recent data suggest PM
emissions are significantly higher than
currently estimated in the MOBILE6
emissions model. In addition, testing
done for this rule demonstrates that PM
emissions are elevated at cold
temperatures. The estimates in Table
V.C–1 do not account for the effects of
cold temperature.
TABLE V.C–1—48-STATE PM2.5 EMISSIONS (TONS) FROM KEY MOBILE SOURCE SECTORS IN 1999, 2010, 2015, AND
2020
[Without this proposed rule]
Category
1999
Light-Duty Gasoline Vehicles and Trucks .......................................................
Heavy-Duty and Other Highway Vehicles .......................................................
Nonroad Equipment .........................................................................................
Section V.E, below, presents estimates
of PM emission reductions associated
with the proposed cold-temperature
vehicle standards.
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D. Description of Current Mobile Source
Emissions Control Programs That
Reduce MSATs
As described in section V.A, existing
mobile source control programs will
reduce MSAT emissions (not including
diesel PM) by 60% between 1999 and
2020. Diesel PM from mobile sources
will be reduced by 70% between 1999
and 2020. The mobile source programs
include controls on fuels, highway
vehicles, and nonroad equipment. These
programs are also reducing
hydrocarbons and PM more generally,
as well as oxides of nitrogen. The
sections immediately below provide
general descriptions of these programs,
as well as voluntary programs to reduce
mobile source emissions, such as the
National Clean Diesel Campaign and
Best Workplaces for Commuters. A more
detailed description of mobile source
programs is provided in Chapter 2 of the
RIA.
48,000
136,000
332,000
1. Fuels Programs
Several federal fuel programs reduce
MSAT emissions. Some of these
programs directly control air toxics,
such as the reformulated gasoline (RFG)
program’s benzene content limit and
required reduction in total toxics
emissions, and the anti-backsliding
requirements of the anti-dumping and
current MSAT programs, which require
that gasoline cannot get dirtier with
respect to toxics emissions. Others, such
as the gasoline sulfur program, control
toxics indirectly by reducing
hydrocarbon and related toxics
emissions.
a. RFG
The RFG program contains two direct
toxics control requirements. The first is
a fuel benzene standard, requiring RFG
to average no greater than 0.95 volume
percent benzene annually (on a refinery
or importer basis). The RFG benzene
requirement includes a per-gallon cap
on fuel benzene level of 1.3 volume
percent. In 1990, when the Clean Air
Act was amended to require
reformulated gasoline, fuel benzene
averaged 1.60 volume percent. For a
variety of reasons, including other
2010
2015
33,000
51,000
232,000
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39,000
20,000
178,000
regulations, chemical product prices
and refining efficiencies, most refiners
and importers have achieved
significantly greater reductions in
benzene than required by the program.
In 2003, RFG benzene content averaged
0.62 percent. The RFG benzene
requirement includes a per-gallon cap
on fuel benzene level of 1.3 volume
percent.
The second RFG toxics control
requires that RFG achieve a specific
level of toxics emissions reduction. The
requirement has increased in stringency
since the RFG program began in 1995,
when the requirement was that RFG
annually achieve a 16.5% reduction in
total (exhaust plus evaporative) air
toxics emissions. Currently, a 21.5%
reduction is required. These reductions
are determined using the Complex
Model. As mentioned above, for a
variety of reasons most regulated parties
have overcomplied with the required
toxics emissions reductions. During
1998–2000, RFG achieved, on average, a
27.5% reduction in toxics emissions.
b. Anti-Dumping
The anti-dumping regulations were
intended to prevent the dumping of
‘‘dirty’’ gasoline components, which
167 PM
2.5 is particulate matter under 2.5 microns
in diameter. Over 85% of the mass of PM from
mobile sources is PM2.5.
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28,000
201,000
2020
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individual MSAT1 baseline, EPA
requires each refiner and importer to
submit documentation supporting the
determination of the baseline. Most
refiners and many importers in business
during the baseline period had
sufficient data to establish an individual
baseline. An MSAT1 baseline volume is
associated with each unique individual
baseline value. The MSAT1 baseline
volume reflects the average annual
volume of such gasoline produced or
imported during the baseline period.
Refiners and importers who did not
have sufficient refinery production or
imports during 1998–2000 to establish a
unique individual MSAT1 baseline
must use the default baseline provided
in the rule.
The MSAT1 program began with the
annual averaging period beginning
January 1, 2002. Since then, the toxics
performance for RFG has improved from
a baseline period average of 27.5%
reduction to 29.5% reduction in 2003.
Likewise, CG toxics emissions have
decreased from an average of 95 mg/
mile during 1998–2000 to 90.7 mg/mile
in 2003.
c. 2001 Mobile Source Air Toxics Rule
(MSAT1)
As discussed above, both RFG and CG
have, on average, exceeded their
respective toxics control requirements.
In 2001, EPA issued a mobile source air
toxics rule (MSAT1, for the purposes of
this second proposal), as discussed in
section I.D. The intent of MSAT1 is to
prevent refiners and importers from
backsliding from the toxics performance
that was being achieved by RFG and CG.
In order to lock in superior levels of
control, the rule requires that the annual
average toxics performance of gasoline
must be at least as clean as the average
performance of the gasoline produced or
imported during the three-year period
1998–2000. The period 1998–2000 is
called the baseline period. Toxics
performance is determined separately
for RFG and CG, in the same manner as
the toxics determinations required by
the RFG 170 and anti-dumping rules.
Like the anti-dumping provisions,
MSAT1 utilizes an individual baseline
against which compliance is
determined. The average 1998–2000
toxics performance level, or baseline, is
determined separately for each refinery
and importer.171 To establish a unique
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were removed to produce RFG, into
conventional gasoline (CG). Since the
dumping of ‘‘dirty’’ gasoline
components, for example, benzene or
benzene-containing blending streams,
would show up as increases in toxics
emissions, the anti-dumping regulations
require that a refiner’s or importer’s CG
be no more polluting with respect to
toxics emissions than the refiner’s or
importer’s 1990 gasoline. The antidumping program considers only
exhaust toxics emissions and does not
include evaporative emissions.168
Refiners and importers have either a
unique individual anti-dumping
baseline or they have the statutory antidumping baseline if they did not fulfill
the minimum requirements for
developing a unique individual
baseline. In 1990, average exhaust toxics
emissions (as estimated by the Complex
Model) were 104.5 mg/mile; 169 in 2004,
CG exhaust toxics emissions averaged
90.7 mg/mile. Although CG has no
benzene limit, benzene levels have
declined significantly from the 1990
level of 1.6 volume percent to 1.1
volume percent for CG in 2004.
d. Gasoline Sulfur
168 See RFG rule for why evaporative emissions
are not included in the anti-dumping toxics
determination.
169 Phase II.
170 40 CFR Part 80, Subpart D.
171 Except for those who comply with the antidumping requirements for conventional gasoline on
an aggregate basis, in which case the MSAT1
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EPA’s gasoline sulfur program 172
requires, beginning in 2006, that sulfur
levels in gasoline can be no higher in
any one batch than 80 ppm, and must
average 30 ppm annually. When fully
effective, gasoline will have 90 percent
less sulfur than before the program.
Reduced sulfur levels are necessary to
ensure that vehicle emission control
systems are not impaired. These systems
effectively reduce non-methane organic
gas (NMOG) emissions, of which some
are air toxics. With lower sulfur levels,
emission control technologies can work
longer and more efficiently. Both new
and older vehicles benefit from reduced
gasoline sulfur levels.
e. Gasoline Volatility
A fuel’s volatility defines its
evaporation characteristics. A gasoline’s
volatility is commonly referred to as its
Reid vapor pressure, or RVP. Gasoline
summertime RVP ranges from about 6–
9 psi, and wintertime RVP ranges from
about 9–14 psi, when additional vapor
is required for starting in cold
temperatures. Gasoline vapors contain a
subset of the liquid gasoline
components, and thus can contain
toxics compounds such as benzene. EPA
has controlled summertime gasoline
RVP since 1989 primarily as a VOC and
requirements for conventional gasoline must be met
on the same aggregate basis (40 CFR Part 80,
Subpart E).
172 65 FR 6822 (February 10, 2000).
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ozone precursor control, which also
results in some toxics pollutant
reductions.
f. Diesel Fuel
In early 2001, EPA issued rules
requiring that diesel fuel for use in
highway vehicles contain no more than
15 ppm sulfur beginning June 1,
2006.173 This program contains
averaging, banking and trading
provisions, as well as other compliance
flexibilities. In June 2004, EPA issued
rules governing the sulfur content of
diesel fuel used in nonroad diesel
engines.174 In the nonroad rule, sulfur
levels are limited to a maximum of 500
ppm sulfur beginning in 2007 (current
levels are approximately 3000 ppm). In
2010, nonroad diesel sulfur levels must
not exceed 15 ppm.
EPA’s diesel fuel requirements are
part of a comprehensive program to
combine engine and fuel controls to
achieve the greatest emission
reductions. The diesel fuel provisions
enable the use of advanced emissioncontrol technologies on diesel vehicles
and engines. The diesel fuel
requirements will also provide
immediate public health benefits by
reducing PM emissions from current
diesel vehicles and engines.
g. Phase-Out of Lead in Gasoline
One of the first programs to control
toxic emissions from motor vehicles was
the removal of lead from gasoline.
Beginning in the mid-1970s, unleaded
gasoline was phased in to replace
leaded gasoline. The phase-out of
leaded gasoline was completed January
1, 1996, when lead was banned from
motor vehicle gasoline. The removal of
lead from gasoline has essentially
eliminated on-highway mobile source
emissions of this highly toxic substance.
2. Highway Vehicle and Engine
Programs
The 1990 Clean Air Act Amendments
set specific emission standards for
hydrocarbons and for PM. Air toxics are
present in both of these pollutant
categories. As vehicle manufacturers
develop technologies to comply with
the hydrocarbon (HC) and particulate
standards (e.g., more efficient catalytic
converters), air toxics are reduced as
well. Since 1990, we have developed a
number of programs to address exhaust
and evaporative hydrocarbon emissions
and PM emissions.
Two of our recent initiatives to
control emissions from motor vehicles
173 66 FR 5002 (January 18, 2001) https://
www.epa.gov/otaq/diesel.html.
174 69 FR 38958 (June 29, 2004).
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and their fuels are the Tier 2 control
program for light-duty vehicles and the
2007 heavy-duty engine rule. Together
these two initiatives define a set of
comprehensive standards for light-duty
and heavy-duty motor vehicles and their
fuels. In both of these initiatives, we
treat vehicles and fuels as a system. The
Tier 2 control program establishes
stringent tailpipe and evaporative
emission standards for light-duty
vehicles and a reduction in sulfur levels
in gasoline fuel beginning in 2004.175
The 2007 heavy-duty engine rule
establishes stringent exhaust emission
standards for new heavy-duty engines
and vehicles for the 2007 model year as
well as reductions in diesel fuel sulfur
levels starting in 2006.176 Both of these
programs will provide substantial
emissions reductions through the
application of advanced technologies.
We expect 90% reductions in PM from
new diesel engines compared to engines
under current standards.
Some of the key earlier programs
controlling highway vehicle and engine
emissions are the Tier 1 and NLEV
standards for light-duty vehicles and
trucks; enhanced evaporative emissions
standards; the supplemental federal test
procedures (SFTP); urban bus standards;
and heavy-duty diesel and gasoline
standards for the 2004/2005 time frame.
3. Nonroad Engine Programs
There are various categories of
nonroad engines, including land-based
diesel engines (e.g., farm and
construction equipment), small landbased spark-ignition (SI) engines (e.g.,
lawn and garden equipment, string
trimmers), large land-based SI engines
(e.g., forklifts, airport ground service
equipment), marine engines (including
diesel and SI, propulsion and auxiliary,
commercial and recreational),
locomotives, aircraft, and recreational
vehicles (off-road motorcycles, ‘‘all
terrain’’ vehicles and snowmobiles).
Chapter 2 of the RIA provides more
information about these programs. As
with highway vehicles, the VOC
standards we have established for
nonroad engines will also significantly
reduce VOC-based toxics from nonroad
engines. In addition, the standards for
diesel engines (in combination with the
stringent sulfur controls on nonroad
diesel fuel) will significantly reduce
diesel PM and exhaust organic gases,
which are mobile source air toxics.
In addition to the engine-based
emission control programs described
below, fuel controls will also reduce
emissions of air toxics from nonroad
175 65
176 66
FR 6697, February 10, 2000.
FR 5001, January 18, 2001.
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engines. For example, restrictions on
gasoline formulation (the removal of
lead, limits on gasoline volatility and
RFG) are projected to reduce nonroad
MSAT emissions because most gasolinefueled nonroad vehicles are fueled with
the same gasoline used in on-highway
vehicles. An exception to this is lead in
aviation gasoline. Aviation gasoline,
used in general (as opposed to
commercial) aviation, is a high octane
fuel used in a relatively small number
of aircraft (those with piston engines).
Such aircraft are generally used for
personal transportation, sightseeing,
crop dusting, and similar activities.
4. Voluntary Programs
In addition to the fuel and engine
control programs described above, we
are actively promoting several voluntary
programs to reduce emissions from
mobile sources, such as the National
Clean Diesel Campaign, anti-idling
measures, and Best Workplaces for
Commuters. While the stringent
emissions standards described above
apply to new highway and nonroad
diesel engines, it is also important to
reduce emissions from the existing fleet
of about 11 million diesel engines. EPA
has launched a comprehensive initiative
called the National Clean Diesel
Campaign, one component of which is
to promote the reduction of emissions in
the existing fleet of engines through a
variety of cost-effective and innovative
strategies. The goal of the Campaign is
to reduce emissions from the 11 million
existing engines by 2014. Emission
reduction strategies include switching
to cleaner fuels, retrofitting engines
through the addition of emission control
devices, and engine replacement. For
example, installing a diesel particulate
filter achieves diesel particulate matter
reductions of approximately 90 percent
(when combined with the use of ultra
low sulfur diesel fuel). The Energy
Policy Act of 2005 includes grant
authorizations and other incentives to
help facilitate voluntary clean diesel
actions nationwide.
The National Clean Diesel Campaign
is focused on leveraging local, state, and
federal resources to retrofit or replace
diesel engines, adopt best practices, and
track and report results. The Campaign
targets five key sectors: School buses,
ports, construction, freight, and
agriculture.
Reducing vehicle idling provides
important environmental benefits. As a
part of their daily routine, truck drivers
often keep their vehicles at idle during
stops to provide power, heat and air
conditioning. EPA’s SmartWay
Transport Partnership is helping the
freight industry to adopt innovative idle
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reduction technologies and take
advantage of proven systems that
provide drivers with basic necessities
without using the engine. To date, there
are 50 stationary anti-idling projects,
and mobile technology has been
installed on nearly 20,000 trucks. The
SmartWay Transport Partnership also
works with the freight industry to
reduce fuel use (with a concomitant
reduction in emissions) by promoting a
wide range of new technologies such as
advanced aerodynamics, single-wide
tires, weight reduction speed control
and intermodal shipping.
Daily commuting represents another
significant source of emissions from
motor vehicles. EPA’s Best Workplaces
for CommutersSM program is working
with employers across the country to
reverse the trend of longer, singleoccupancy vehicle commuting. OTAQ
has created a national list of the Best
Workplaces for Commuters to formally
recognize employers that offer superior
commuter benefits such as free transit
passes, subsidized vanpools/carpools,
and flexi-place, or work-from-home,
programs. More than 1,300 employers
representing 2.8 million U.S. workers
have been designated Best Workplaces
for Commuters.
Much of the growth in the Best
Workplaces for Commuters program has
been through metro area-wide
campaigns. Since 2002, EPA has worked
with coalitions in 14 major metropolitan
areas to increase the penetration of
commuter benefits in the marketplace
and the visibility of the companies that
have received the BWC designation.
Another significant path by which the
program has grown is through
Commuter Districts including corporate
and industrial business parks, shopping
malls, business improvement districts
and downtown commercial areas. To
date EPA has granted the Best
Workplaces for Commuters ‘‘District’’
designation to twenty locations across
the country including downtown
Denver, Houston, Minneapolis and
Tampa.
E. Emission Reductions From Proposed
Controls
1. Proposed Vehicle Controls
We are proposing a hydrocarbon
standard for gasoline passenger vehicles
at cold temperatures. This standard will
reduce VOC at temperatures below 75
°F, including air toxics such as benzene,
1,3-butadiene, formaldehyde,
acetaldehyde, acrolein and naphthalene,
and will also reduce emissions of direct
and secondary PM. We are also
proposing new evaporative emissions
standards for Tier 2 vehicles starting in
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2009. These new evaporative standards
reflect the emissions levels already
being achieved by manufacturers.
a. Volatile Organic Compounds (VOC)
Table V.E–1 shows the VOC exhaust
emission reductions from light-duty
gasoline vehicles and trucks that would
result from our proposed standards. The
proposed standards would reduce VOC
emissions in 2030 by 32%. Overall VOC
exhaust emissions from these vehicles
would be reduced by 81% between 1999
and 2030 (including the effects of the
proposed standards as well as standards
already in place, such as Tier 2).
TABLE V.E–1.—ESTIMATED NATIONAL REDUCTIONS IN EXHAUST VOC EMISSIONS FROM LIGHT-DUTY GASOLINE VEHICLES
AND TRUCKS, 1999 TO 2030
1999
VOC Without Rule (tons) .................................................................................
VOC With Proposed Vehicle Standards (tons) ...............................................
VOC Reductions from Proposed Vehicle Standards (tons) ............................
Percentage Reduction .....................................................................................
2015
2020
2030
4,899,891
N.A
N.A
N.A
2,625,076
2,305,202
319,874
12
2,556,751
2,020,267
536,484
21
2,899,269
1,985,830
913,439
32
result in a 38% reduction in benzene
emissions and 37% reduction in total
emissions of the MSATs 177 from light-
b. Toxics
In 2030, we estimate that the
proposed vehicle standards would
duty vehicles and trucks (see Tables
V.E–2 and V.E–3).
TABLE V.E–2.—ESTIMATED NATIONAL REDUCTIONS IN BENZENE EXHAUST EMISSIONS FROM LIGHT-DUTY GASOLINE
VEHICLES AND TRUCKS, 1999 TO 2030
1999
Benzene Without Rule (tons) ..........................................................................
Benzene With Proposed Vehicle Standards (tons) .........................................
Benzene Reductions from Proposed Vehicle Standards (tons) ......................
Percentage Reduction .....................................................................................
171,154
N.A.
N.A.
N.A.
2015
2020
101,355
84,496
16,859
17
106,071
77,966
28,105
26
2030
124,897
77,208
47,689
38
TABLE V.E–3.—ESTIMATED NATIONAL REDUCTIONS IN EXHAUST MSAT EMISSIONS FROM LIGHT-DUTY GASOLINE
VEHICLES AND TRUCKS, 1999 TO 2030
1999
MSATs Without Rule (tons) .............................................................................
MSATs With Proposed Vehicle Standards (tons) ...........................................
MSAT Reductions from Proposed Vehicle Standards (tons) ..........................
Percentage Reduction .....................................................................................
c. PM2.5
EPA expects that the proposed coldtemperature vehicle standards would
reduce exhaust emissions of direct PM2.5
by over 20,000 tons in 2030 nationwide
(see Table V.E–4 below). Our analysis of
the data from vehicles meeting Tier 2
emission standards indicate that PM
emissions follow a monotonic
1,341,572
N.A.
N.A.
N.A.
relationship with temperature, with
lower temperatures corresponding to
higher vehicle emissions. Additionally,
the analysis shows the ratio of PM to
total non-methane hydrocarbons
(NMHC) to be independent of
temperature.178 Our testing indicates
that strategies which reduce NMHC start
emissions at cold temperatures also
reduce direct PM emissions. Based on
2015
2020
707,877
599,492
108,385
15
724,840
543,332
181,509
25
2030
844,366
535,479
308,887
37
these findings, direct PM emissions at
cold temperatures were estimated using
a constant PM to NMHC ratio. PM
emission reductions were estimated by
assuming that NMHC reductions will
result in proportional reductions in PM.
This assumption is supported by test
data. For more detail, see Chapter 2.1 of
the RIA.
TABLE V.E–4.—ESTIMATED NATIONAL REDUCTIONS IN DIRECT PM2.5 EXHAUST EMISSIONS FROM LIGHT-DUTY GASOLINE
VEHICLES AND TRUCKS, 2015 TO 2030
2015
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PM2.5 Reductions from Proposed Vehicle Standards (tons) .......................................................
2. Proposed Fuel Benzene Controls
evaporative emissions from both onroad and nonroad mobile sources that
are fueled by gasoline. In addition, the
The proposed fuel benzene controls
would reduce benzene exhaust and
177 Table IV.A–1 lists the MSATs included in this
analysis.
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7,037
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20,096
proposed fuel benzene standard would
reduce evaporative emissions from
gasoline distribution and gas cans.
178 U.S. EPA. 2005. Cold-temperature exhaust
particulate matter emissions. Memorandum from
Chad Bailey to docket EPA–HQ–OAR–2005–0036.
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2030
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Impacts on 1,3-butadiene,
formaldehyde, and acetaldehyde
emissions are not significant, but are
presented in Chapter 2 of the RIA. We
do not expect the fuel benzene standard
to have quantifiable impacts on any
other air toxics, total VOCs, or PM.
Table V.E–5 shows national estimates
of total benzene emissions from these
source sectors with and without the
proposed fuel benzene standard. These
estimates do not include effects of the
proposed vehicle or gas can standards
(see section V.E.4 for the combined
15839
effects of the controls). The proposed
fuel benzene standard would reduce
total benzene emissions from on-road
and nonroad gasoline mobile sources,
gas cans, and gasoline distribution by
12% in 2015.
TABLE V.E–5.—ESTIMATED REDUCTIONS IN BENZENE EMISSIONS FROM PROPOSED GASOLINE STANDARD BY SECTOR IN
2015
Gasoline onroad mobile
sources
Benzene Without Rule (tons) ...............................................
Benzene With Proposed Gasoline Standard (tons) ............
Benzene Reductions from Proposed Gasoline Standard
(tons) ................................................................................
Percentage Reduction .........................................................
3. Proposed Gas Can Standards
a. VOC
Table V.E–6 shows the reductions in
VOC emissions that we expect from the
Gasoline
nonroad mobile sources
Gas cans
Gasoline
distribution
Total
103,797
92,513
37,747
33,247
2,262
1,359
5,999
4,054
149,805
131,173
11,284
11
4,500
12
903
40
1,945
32
18,632
12
proposed gas can standard. In 2015,
VOC emissions from gas cans would be
reduced by 60% because of reduced
permeation, spillage, and evaporative
losses. These estimates do not include
the effects of a fuel benzene standard
(see section V.E.4 for the combined
effects of the proposed controls).
TABLE V.E–6.—ESTIMATED NATIONAL REDUCTIONS IN VOC EMISSIONS FROM GAS CANS, 2010 TO 2030
1999
VOC Without Rule (tons) .....................................................
VOC With Proposed Gas Can Standard (tons) ...................
VOC Reductions from Proposed Gas Can Standard (tons)
Percentage Reduction .........................................................
b. Toxics
The proposed gas can standard would
reduce emissions of benzene,
naphthalene, toluene, xylenes,
ethylbenzene, n-hexane, 2,2,4-
2010
318,596
N.A.
N.A.
N.A.
2015
279,374
250,990
28,384
10
trimethylpentane, and MTBE. We
estimate that benzene emissions from
gas cans would be reduced by 65% (see
Table V.E–7) and, more broadly, air
toxic emissions by 61% (see Table V.E–
8) in year 2015. These reductions do not
2020
296,927
116,431
180,496
61
318,384
125,702
192,683
61
2030
362,715
144,634
218,080
60
include effects of the proposed fuel
benzene standard (see section V.E.4 for
the combined effects of the proposed
controls). Chapter 2 of the RIA provides
details on the emission reductions of the
other toxics.
TABLE V.E–7.—ESTIMATED NATIONAL REDUCTIONS IN BENZENE EMISSIONS FROM GAS CANS, 2010 TO 2030
1999
Benzene Without Rule (tons) ...............................................
Benzene With Proposed Gas Can Standard (tons) ............
Benzene Reductions from Proposed Gas Can Standard
(tons) ................................................................................
Percentage Reduction .........................................................
2010
2015
2020
2030
2,229
N.A.
2,118
1,885
2,262
794
2,423
856
2,757
985
N.A.
N.A.
233
11
1,468
65
1,567
65
1,772
64
TABLE V.E–8.—ESTIMATED NATIONAL REDUCTIONS IN TOTAL MSAT EMISSIONS FROM GAS CANS, 2010 TO 2030
1999
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MSATs Without Rule (tons) .................................................
MSATs With Proposed Gas Can Standard (tons) ...............
MSAT Reductions from Proposed Gas Can Standard
(tons) ................................................................................
Percentage Reduction .........................................................
Chapter 2 of the RIA describes how
we estimated emissions from gas cans,
including the key assumptions used and
uncertainties in the analysis. We request
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2010
Frm 00037
2020
2030
39,581
N.A.
34,873
31,312
37,076
14,445
39,751
15,593
45,284
17,942
N.A.
N.A.
3,561
10
22,631
61
24,158
61
27,342
60
comments on the emissions inventory
methodology used by EPA and we
encourage commenters to provide
relevant data where possible.
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4. Total Emission Reductions From
Proposed Controls
Sections V.E.1 through V.E.3 present
the emissions impacts of each of the
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proposed controls individually. This
section presents the combined
emissions impacts of the proposed
controls.
a. Toxics
Air toxic emissions from light-duty
vehicles depend on both fuel benzene
content and vehicle hydrocarbon
emission controls. Similarly, the air
toxic emissions from gas cans depend
on both fuel benzene content and the
gas can emission controls. Tables V.E–
9 and V.E–10 below summarize the
expected reductions in benzene and
MSAT emissions, respectively, from our
proposed vehicle, fuel, and gas can
controls. In 2030, annual benzene
emissions from gasoline on-road mobile
sources would be 44% lower as a result
of this proposal (see Figure V.E–1).
Annual benzene emissions from
gasoline light-duty vehicles would be
45% lower in 2030 as a result of this
proposal. Likewise, this proposal would
reduce annual emissions of benzene
from gas cans by 78% in 2030 (see
Figure V.E–2). For MSATs from on-road
mobile sources, Figure V.E–3 below
shows a 33% reduction in MSAT
emissions in 2030.
TABLE V.E–9.—ESTIMATED REDUCTIONS IN BENZENE EMISSIONS FROM PROPOSED CONTROL MEASURES BY SECTOR,
2015 TO 2030
2015
Benzene
Gasoline On-road Mobile
Sources ..............................
Gasoline Nonroad Mobile
Sources ..............................
Gas Cans ..............................
Gasoline Distribution .............
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Total ...............................
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1999
Without
rule (tons)
With rule
(tons)
2020
Reductions
(tons)
Without
rule (tons)
With rule
(tons)
2030
Reductions
(tons)
Without
rule (tons)
With rule
(tons)
Reductions
(tons)
178,465
103,798
77,155
26,643
108,256
71,326
36,930
127,058
70,682
56,376
58,710
2,229
5,502
37,747
2,262
5,999
33,247
492
4,054
4,500
1,770
1,945
36,440
2,423
6,207
32,018
531
4,210
4,422
1,892
1,997
39,162
2,757
6,207
34,400
610
4,210
4,762
2,147
1,997
244,905
149,806
114,948
34,858
153,326
108,085
45,241
175,184
109,902
65,282
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TABLE V.E–10.—ESTIMATED REDUCTIONS IN MSAT EMISSIONS FROM PROPOSED CONTROL MEASURES BY SECTOR,
2015 TO 2030
2015
Gasoline On-road Mobile
Sources ..............................
Gasoline Nonroad Mobile
Sources ..............................
Gas Cans ..............................
Gasoline Distribution .............
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Total ...............................
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1999
Without
rule (tons)
With rule
(tons)
2020
Reductions
(tons)
Without
rule (tons)
With rule
(tons)
2030
Reductions
(tons)
Without
rule (tons)
With rule
(tons)
Reductions
(tons)
1,415,502
731,283
613,227
118,056
745,769
555,541
190,228
865,767
548,298
317,469
673,922
39,581
50,625
432,953
37,076
62,804
428,506
14,143
60,859
4,447
22,933
1,945
390,468
39,751
64,933
386,095
15,268
62,936
4,373
24,483
1,997
405,119
45,284
64,933
400,408
17,567
62,936
4,711
27,717
1,997
2,179,630
1,264,116
1,116,735
147,381
1,240,921
1,019,840
221,081
1,381,103
1,029,209
351,894
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MSAT
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b. VOC
VOC emissions would be reduced by
the hydrocarbon emission standards for
both light-duty vehicles and gas cans.
As seen in the table and accompanying
figure below, annual VOC emission
reductions from both of these sources
would be 35% lower in 2030 because of
proposed control measures.
TABLE V.E–11.—ESTIMATED REDUCTIONS IN VOC EMISSIONS FROM LIGHT-DUTY GASOLINE VEHICLES AND GAS CANS,
2015 TO 2030
c. PM2.5
We expect that only the proposed
vehicle control would reduce emissions
of direct PM2.5. As shown in Table V.E–
4, we expect this control to reduce
direct PM2.5 emissions by about 20,000
tons in 2030. In addition, the VOC
reductions from the proposed vehicle
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and gas can standards would also
reduce secondary formation of PM2.5.
F. How Would This Proposal Reduce
Exposure to Mobile Source Air Toxics
and Associated Health Effects?
The proposed benzene standard for
gasoline would reduce both evaporative
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2030
2,922,003
2,421,633
500,370
2,875,135
2,145,969
729,168
3,261,984
2,130,464
1,131,520
and exhaust emissions from motor
vehicles and nonroad equipment. It
would also reduce emissions from gas
cans and stationary source emissions
associated with gasoline distribution.
Therefore, it would reduce exposure to
benzene for the general population, and
also for people near roadways, in
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VOC Without Rule (tons) .............................................................................................................
VOC With Proposed Vehicle and Gas Can Standards (tons) ....................................................
VOC Reduction (tons) .................................................................................................................
2020
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2015
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vehicles, in homes with attached
garages, operating nonroad equipment,
and living or working near sources of
gasoline distribution emissions (such as
bulk terminals, bulk plants, tankers,
marine vessels, and service stations).
Section IV.B.2 of this preamble provides
more details on these types of
exposures.
We performed national-scale air
quality, exposure, and risk modeling in
order to quantitatively assess the
impacts of the proposed fuel benzene
standard. However, in addition to the
limitations of the national-scale
modeling tools (discussed in section
IV.A), this modeling did not account for
the elevated hydrocarbon emissions
from motor vehicles at cold
temperatures, which we recently
discovered and are further described in
section VI and the RIA. The modeling
also examined the gasoline benzene
standard alone, without the proposed
vehicle or gas can standards.
Nevertheless, the modeling is useful as
a preliminary assessment of the impacts
of the fuel standard.
The fuel benzene standard being
proposed in this rule would reduce both
the number of people above the 1 in
100,000 increased cancer risk level, and
the average population cancer risk, by
reducing exposures to benzene from
mobile sources. The number of people
above the 1 in 100,000 cancer risk level
due to exposure to all mobile source air
toxics from all sources would decrease
by over 3 million in 2020 and by about
3.5 million in 2030, based on average
census tract risks. The number of people
above the 1 in 100,000 increased cancer
risk level from exposure to benzene
from all sources would decrease by over
4 million in 2020 and 5 million in 2030.
It should be noted that if it were
possible to estimate impacts of the
proposed standard on ‘‘background’’
concentrations, the estimated overall
risk reductions would be even larger.
The proposed standard would have
little impact on the number of people
above various respiratory hazard index
levels, since this potential non-cancer
risk is dominated by exposure to
acrolein.
Table V.F–1 depicts the impact on the
mobile source contribution to
nationwide average population cancer
risk from benzene in 2020. Nationwide,
the cancer risk attributable to mobile
source benzene would be reduced by
over 8%. Reductions in areas not subject
to reformulated gasoline controls are
almost 13 percent relative to risks
without the proposed control; and in
some states with high fuel benzene
levels, such as Minnesota and
Washington, the risk reduction would
exceed 17 percent. In Alaska, which has
the highest fuel benzene levels in the
country, reductions would exceed 30%.
Reductions for other modeled years are
similar. The methods and assumptions
used to model the impact of the
proposed control are described in more
detail in the Regulatory Impact
Analysis. Although not quantified in the
risk analyses for this rule, controls
proposed for portable fuel containers
will also reduce exposures and risk from
benzene, and cold temperature
hydrocarbon standards for exhaust
emissions will reduce cancer and
noncancer risks for all gaseous mobile
source air toxics. These reductions will
vary geographically since reductions
from vehicle control are higher at colder
temperatures, and reductions from gas
can controls are higher at higher
temperatures.
TABLE V.F–1.—IMPACT OF PROPOSED FUEL BENZENE CONTROL ON THE MOBILE SOURCE CONTRIBUTION TO NATIONWIDE
AVERAGE POPULATION CANCER RISK IN 2020
U.S.
Without Proposal .........................................................................................................................
0.62% Benzene Standard ............................................................................................................
% Reduction ................................................................................................................................
Table V.F–2 summarizes the change
in median and 95th percentile benzene
inhalation cancer risk from all outdoor
sources in 2015, 2020, and 2030, with
the fuel benzene controls proposed in
this rule. The reductions in risk would
be larger if the modeling fully accounted
for a number of factors, including:
benzene emissions at cold temperature;
exposure to benzene emissions from
Non-RFG
areas
RFG areas
2.57×10¥6
2.35×10¥6
8.6
3.64×10¥6
3.51×10¥6
3.6
1.96×10¥6
1.72×10¥6
12.2
vehicles, equipment, and gas cans in
attached garages; near-road exposures;
and the impacts of the control program
on ‘‘background’’ levels attributable to
transport.
TABLE V.F–2.—CHANGE IN MEDIAN AND 95TH PERCENTILE BENZENE INHALATION CANCER RISK FROM OUTDOOR
SOURCES IN 2015, 2020, AND 2030 WITH THE FUEL BENZENE CONTROLS PROPOSED IN THIS RULE
2015
median
5.73×10¥6
5.49×10¥6
4.2
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Current Controls .......................................
Proposed Benzene Standard ...................
Percent Change .......................................
We did not model the air quality,
exposure, and risk impacts of the
proposed vehicle and gas can standards.
However, the proposed vehicle
standards would reduce exposure to
several MSATs, including benzene. Like
the proposed fuel standard, the vehicle
standards would reduce the general
population’s exposure to MSATs, as
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2020
95th
median
1.38×10¥5
1.32×10¥5
4.3
5.61×10¥6
5.39×10¥6
3.9
well as people near roadways and in
vehicles. Since motor vehicle emissions
are ubiquitous across the U.S. and
widely dispersed, reductions in
exposure and risk will be approximately
proportional to reductions in emissions.
The gas can standard will reduce
evaporative emissions of several
MSATs, including benzene. We expect
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that these standards would significantly
reduce concentrations of benzene and
other MSATs in attached garages and
inside homes with attached garages.
Accordingly, exposure to benzene and
other MSATs would be significantly
reduced. As discussed in section IV.B.2,
exposures to emissions occurring in
attached garages can be quite high.
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The proposed vehicle and gas can
standards would also reduce precursors
to ozone and PM. We have modeled the
ozone impacts of the proposed gas can
standard and the PM health benefits that
would be associated with the direct PM
reductions from the proposed vehicle
standards. These results are discussed
in sections IV.D and IX, respectively.
G. Additional Programs Under
Development That Will Reduce MSATs
1. On-Board Diagnostics for Heavy-Duty
Vehicles Over 14,000 Pounds
We are planning to propose on-board
diagnostics (OBD) requirements for
heavy-duty vehicles over 14,000
pounds. In general, OBD systems
monitor the operation of key emissions
controls to detect major failures that
would lead to emissions well above the
standards during the life of the vehicle.
Given the nature of the heavy-duty
trucking industry, 50-state
harmonization of emissions requirement
is an important consideration. In order
to work towards this goal, the Agency
signed a Memorandum of Agreement in
2004 with the California Air Resources
Board which expresses both agencies’
interest in working towards a single,
nationwide program for heavy-duty
OBD. Since that time, California has
established their heavy-duty OBD
program, which will begin
implementation in 2010. We expect the
Agency’s program will also begin in the
2010 time frame. These requirements
would help ensure that the emission
reductions we projected in the 2007
rulemaking for heavy-duty engines
occur in-use.
2. Standards for Small SI Engines
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We are developing a proposal for
Small SI engines (those typically used
in lawn and garden equipment) and
recreational marine engines. This
proposal is being developed in response
to Section 428 of the Omnibus
Appropriations Bill for 2004, which
requires EPA to propose regulations
under Clean Air Act section 213 for new
nonroad spark-ignition engines under
50 horsepower. We plan to propose
standards that would further reduce the
emissions for these nonroad categories,
and we anticipate that the new
standards would provide significant
further reductions in HC (and VOCbased toxics) emissions.
3. Standards for Locomotive and Marine
Engines
In addition, we are planning to
propose more stringent standards for
large diesel engines used in locomotive
and marine applications, as discussed in
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a recent Advance Notice of Proposed
Rulemaking.179 New standards for
marine diesel engines would apply to
engines less than 30 liters per cylinder
in displacement (all engine except for
Category 3). We are considering
standards modeled after our Tier 4
nonroad diesel engine program, which
achieve substantial reductions in PM,
HC, and NOX emissions. These
standards would be based on the use of
high efficiency catalyst aftertreatment
and would also require fuel sulfur
control. As discussed in our recent
ANPRM, we are considering
implementation as early as 2011.
VI. Proposed New Light-Duty Vehicle
Standards
A. Why Are We Proposing New
Standards?
1. The Clean Air Act and Air Quality
As described in section V of this
preamble, the U.S. has made significant
progress in reducing emissions from
passenger cars and light trucks since the
passage of the 1990 Clean Air Act
Amendments. Many emission control
programs adopted to implement the
1990 Clean Air Act Amendments are
reducing and will continue to reduce air
toxics from light-duty vehicles. These
include our reformulated gasoline (RFG)
program, our Supplemental Federal Test
Procedure (SFTP) standards, our
national low emission vehicle program
(NLEV), and, most recently, our Tier 2
motor vehicle emissions standards and
gasoline sulfur control requirements.180
While these vehicle programs were put
in place primarily to reduce ambient
concentrations of criteria pollutants and
their precursors (NOX, VOC, CO, and
PM), they have reduced and will
continue to significantly reduce lightduty vehicle emissions of air toxics. For
example, there are numerous chemicals
that make up total VOC emissions,
including several gaseous toxics (e.g.,
benzene, formaldehyde, 1,3-butadiene,
and acetaldehyde). These toxics are all
reduced by VOC emissions standards. It
is the stringent control of hydrocarbons
in particular that results in stringent
control of gaseous toxics. There are no
vehicle-based technologies of which we
are aware that reduce these air toxics
individually.
At the time of our 2001 MSAT rule,
we had recently finalized the Tier 2
179 69
FR 39276, June 29, 2004.
180 Unless otherwise noted, we use ‘‘light-duty
vehicles’’ or ‘‘vehicles’’ to generally refer to
passenger vehicles, light-duty trucks such as sport
utility vehicles (SUVs) and pick-ups, and mediumduty passenger vehicles (MDPVs) which includes
larger SUVs and passenger vans up to 10,000
pounds Gross Vehicle Weight Rating.
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emissions standards and gasoline sulfur
control requirements (described in more
detail below in section V.D). As
explained earlier, we concluded then
under section 202(l) that the Tier 2
standards represented the greatest
degree of emissions control achievable
for those vehicles. However, we also
committed to continue to consider the
feasibility of additional vehicle-based
MSAT controls in the future.
2. Technology Opportunities for LightDuty Vehicles
Since the 2001 MSAT rule, we have
identified potential situations where
further reductions of light-duty vehicle
hydrocarbon emissions—and, therefore,
mobile source air toxics—are
technically feasible, cost-effective, and
do not have adverse energy or safety
implications. First, recent research and
analytical work shows that the Tier 2
exhaust emission standards for
hydrocarbons (which are typically
tested at 75° F) do not, in the case of
many vehicles, result in robust control
of hydrocarbon emissions at lower
temperatures. We believe that cold
temperature hydrocarbon control can be
substantially improved using the same
technological approaches generally
already in use in the Tier 2 vehicle fleet
to meet the stringent standards at 75° F.
Second, we believe that harmonization
of evaporative emission standards with
California would prevent backsliding by
codifying current industry practices.
Sections VI.B.1 and VI.B.2, below,
provide our rationale for proposing new
cold temperature and evaporative
controls and describe the detailed
provisions of our proposal. We request
comment on all aspects of these
proposals and encourage commenters to
provide detailed rationales and
supporting data where possible.
Aside from these proposed standards,
we continue to believe that the
remaining Tier 2 exhaust emission
standards (i.e., those that apply over the
standard Federal Test Procedure at
temperatures between 68° F and 86° F)
represent the greatest emissions
reductions achievable as required under
Clean Air Act section 202(l). We
therefore are not proposing further
emission reductions from these
vehicles. (Please see section VI.D for
further discussion.)
3. Cold Temperature Effects on
Emission Levels
a. How Does Temperature Affect
Emissions?
With the possible exception of highload operation, Tier 2 gasoline-powered
vehicles emit the overwhelming
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majority of hydrocarbon emissions in
the first few minutes of operation
following a cold start (i.e., starting the
vehicles after the engine has stabilized
to the ambient temperatures, such as
overnight). This is true at all cold start
temperatures, and the general trend is
that hydrocarbon emissions
progressively increase as engine start
temperatures decrease. The level of
hydrocarbon emissions produced by the
engine will vary with start temperature,
engine hardware design and most
importantly, engine management
control strategies. Furthermore, due to
the heavy dependence on the
aftertreatment system to perform the
main emission reducing functions, any
delayed or non-use of emission controls
(hardware or software) will further
increase the amount of hydrocarbon
emissions emitted from the vehicle
following the cold start.
Elevated hydrocarbon levels at cold
temperatures, specifically, the nonmethane hydrocarbons (NMHC) portion
of total hydrocarbons (THC), also
indicate higher emissions of gaseous air
toxics. A detailed description of the
relationship between NMHC and air
toxics can be found in Chapter 2 of the
RIA. Recent EPA research studies 181 on
Tier 2 gasoline vehicles, and past EPA
studies 182 on older generation gasoline
vehicles, demonstrate that many air
toxics (e.g., benzene) are a relatively
constant fraction of NMHC. This
relationship is observed regardless of
vehicle type, NMHC emissions level, or
temperature. The relationship remains
relatively constant for different vehicles
with different levels of NMHC
emissions, and for the same vehicle at
colder temperatures. Therefore, it can be
concluded that reductions in NMHC
will result in proportional reductions in
gaseous air toxics which are
components of HC. These observations
and findings indicate that controlling
NMHC is an effective approach to
reducing toxics which are a component
of NMHC, including benzene emissions.
In addition to control of air toxics,
another benefit of regulating NMHC at
cold temperatures is reductions in
particulate matter (PM). PM is a criteria
pollutant and for gasoline-fueled
vehicles is an emerging area of interest
on which we are continuing to collect
data (see sections III.E and IV.F for more
details on PM). We have limited data
indicating that PM emissions can be
significantly higher at cold temperatures
b. What Are the Current Emissions
Control Requirements?
There are several requirements
currently in place that have resulted in
significant NMHC reductions and
provided experience with control
strategies that apply across a broad
range of in-use driving conditions,
including cold temperatures. These
requirements include the Tier 2
standards, the Supplemental Federal
Test Procedure (SFTP) standards, the
cold temperature carbon monoxide (CO)
standard, and the California 50° F
hydrocarbon standard.
The Tier 2 program (and, before that,
the NLEV program) contains stringent
new standards for light-duty vehicles
that have resulted in significant
hydrocarbon reductions. To meet these
standards, vehicle manufacturers have
responded with emissions control
hardware and control strategies that
have very effectively minimized
emissions, particularly immediately
following the vehicle start-up. In
addition, the SFTP rule (effective
beginning in model year 2001)
significantly expanded the area of
operation where stringent emission
control was required, by adding a high
load/speed cycle (US06) and an air
conditioning cycle (SC03). Vehicle
manufacturers responded with
additional control strategies across a
broader range of in-use driving
conditions to successfully meet SFTP
requirements.
We also have cold temperature carbon
monoxide (CO) standards which began
in model year 1994 for light-duty
vehicles (LDVs) and light-duty trucks
(LDTs).183 This program requires
manufacturers to comply with a 20° F
CO standard. The 20° F cold CO test
replicates the 75° F FTP drive cycle, but
at the colder temperature. While the
181 ‘‘VOC/PM Cold Temperature Characterization
and Interior Climate Control Emissions/Fuel
Economy Impact,’’ Volume I and II, October 2005.
182 ‘‘Characterization of Emissions from
Malfunctioning Vehicles fueled with Oxygenated
Gasoline-Ethanol (E10) Fuel,’’ Part I, II and III.
183 57 FR 31888 ‘‘Control of Air Pollution from
New Motor Vehicles and New Motor Vehicle
Engines: Cold Temperature Carbon Monoxide
Emissions from 1994 and Later Model Year
Gasoline-Fueled Light-Duty Vehicles and LightDuty Trucks’’, Final Rule, July 17, 1992.
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compared to emissions at the 68–86° F
testing temperatures used in the FTP.
Data also indicate that HC and direct
PM emissions correlate fairly well as
temperature changes and that some
direct PM emissions reductions can be
expected when VOCs are reduced. Also,
from a technological standpoint, we can
expect reductions in PM as
manufacturers reduce over-fueling at
cold temperatures for NMHC control.
Although section 202(l) deals with
control of air toxics, and not criteria
pollutants like PM, this co-benefit of
cold temperature control is significant.
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recent Tier 2 program is primarily
designed to reduce ozone, the cold CO
requirement was enacted to address
exceedances of the national ambient air
quality standards (NAAQS) for CO,
which were mostly occurring during the
cold weather months. While the cold
CO standard was considered
challenging at its introduction,
manufacturers quickly developed
emission control strategies and today
comply with the standard with
generally large compliance margins.
This indicates that manufacturers do in
fact have experience with emission
control strategies at colder temperatures.
Under the Low Emission Vehicle
(LEV) programs, California implemented
stringent emissions standards for a 50°
F FTP test condition in addition to
stringent 75° F standards. By creating a
unique 50° F standard, California
ensures that emission control strategies
successfully used at 75° F are also
utilized at the slightly cooler
temperatures that encompass a larger
range of California’s expected climates.
The 50° F non-methane organic gases
(NMOG) standards are directly
proportional to the 75° F certification
standard; that is, they are two times the
75° F standard. These standards have
resulted in proportional emissions
improvements at 50° F for vehicles
certified to the California standards, as
observed in the manufacturer
certification data. Manufacturers have
met the standards and have successfully
obtained these proportional
improvements at 50° F by implementing
the same emission control strategies
developed for 75° F requirements.
c. Opportunities for Additional Control
As emissions standards have become
more stringent from Tier 1 to NLEV, and
now to Tier 2, manufacturers have
concentrated primarily on emissions
performance just after the start of the
engine in order to further reduce
emissions. To comply with stringent
hydrocarbon emission standards at 75°
F, manufacturers developed new
emission control strategies and practices
that resulted in significant emissions
reductions at that start temperature. For
California, the LEV II program contains
a standard at 50° F (as just explained),
which essentially requires proportional
control of hydrocarbon emissions down
to that temperature. On the national
level, even though there is no explicit
requirement, we expected that
proportional reductions in hydrocarbon
emissions would occur at other colder
start temperatures—including the 20° F
Cold CO test point—as a result of the
more stringent NLEV and Tier 2
standards. We believe that there is no
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engineering reason why proportional
control should not be occurring on a
widespread basis.
However, reported annual
manufacturer certification results
(discussed in the next paragraph)
indicate that for many engine families,
very little improvement in hydrocarbon
emissions was realized at the colder 20°
F Cold CO test conditions, despite the
improved emission control systems
designed for the vehicle under normal
75° F test conditions. Thus although all
vehicle manufacturers have been highly
successful at reducing emissions at the
required FTP start temperature range, in
general, they do not appear to be
capitalizing on NMHC emission control
strategies and technologies at lower
temperatures.
Certification reports submitted by
manufacturers for recent model years of
light duty vehicles in fact show a sharp
rise in hydrocarbon 184 emissions at 20°
F when compared to the reported 75° F
hydrocarbon emission levels. Any rise
in hydrocarbon emissions, specifically
NMHC, will result in proportional rise
in VOC-based air toxics 185. While some
increase in NMHC emissions can be
expected simply due to combustion
limitations of gasoline engines at colder
temperatures, the reported levels of
hydrocarbon emissions seem to indicate
a significantly diminished use of
hydrocarbon emissions controls
occurring at colder temperatures. For
example, on recent Tier 2 certified
vehicles, the reported 20° F
hydrocarbon levels on average were 10
to 12 times higher than the equivalent
vehicle’s measured 75° F hydrocarbon
levels. Some vehicles which were
certified to more stringent Tier 2 bins
(bins 2, 3, and 4) demonstrated 20° F
hydrocarbon levels no different than
less stringent Tier 2 bins (bins 5, 6, 7,
and 8), likewise suggesting no
discernable attempt to use the 75° F
hydrocarbon controls at the 20° F
temperature. On the other hand, in some
select cases, individual vehicles did
demonstrate proportional improvements
in hydrocarbon emission results at 20°
F relative to their 75° F results,
confirming our belief that proportional
control is feasible and indeed is
occasionally practiced. One
manufacturer’s certification results
reflected proportional improvements
184 Most certification 20° F hydrocarbon levels are
reported as THC, but NMHC accounts for
approximately 95% of THC as seen in results with
both THC and NMHC levels reported. This
relationship also is confirmed in EPA test programs
supporting this rule-making.
185 ‘‘VOC/PM Cold Temperature Characterization
and Interior Climate Control Emissions/Fuel
Economy Impact’’, Volume I and II, October 2005.
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across almost its entire vehicle lines
(including vehicles up to 5665 GVWR),
further supporting that proportional
control is feasible.
the Cold CO test, which already requires
hydrocarbon measurement.188
The separate fleet average standards
are proposed to address challenges
related to vehicle weight. We examined
B. What Cold Temperature
the certification data from interim nonRequirements Are We Proposing?
Tier 2 vehicles (i.e., vehicles not yet
phased in to the final Tier 2 program,
1. NMHC Exhaust Emissions Standards
but meeting interim standards
We are proposing a set of standards
established by Tier 2), and we
that will achieve proportional NMHC
determined that there was a general
control from the 75° F Tier 2 standards
trend of increasing hydrocarbon levels
to the 20° F test point. The proposed
with heavier GVWR vehicles. Heavier
standard would achieve the greatest
vehicles generally produce higher levels
degree of hydrocarbon emissions
of emissions for several reasons. First,
reductions feasible by fully utilizing the added weight results in additional work
substantial existing emission control
required to accelerate the vehicle mass.
hardware required to meet Tier 2
This generally results in higher
standards. We believe these standards
emissions, particularly early in the test
would be achievable through calibration right after engine start-up. Second, the
and software control strategies on Tier
design of these vehicle emission control
2 level vehicles without use of
systems may incorporate designs for
additional hardware. The proposed
heavy work (i.e., trailer towing) that
standards are shown in Table VI.B–1.
may put them at some disadvantage at
20° F cold starts. For example, the
TABLE VI.B–1.—PROPOSED 20° F
catalyst may be located further away
FTP EXHAUST EMISSION STANDARDS from the engine so it is protected from
high exhaust temperatures. This catalyst
NMHC
placement may delay the warm-up of
salesthe catalyst, especially at colder
weighted
temperatures. Therefore, we believe a
Vehicle GVWR and category
fleet average standstandard that is higher than the 0.3
ard (grams/ g/mile level proposed for vehicles below
mile)
6,000 lbs GVWR, is what is technically
feasible for heavier vehicles. The
≤ 6000 lbs: Light-duty vehicles
proposed 0.5 g/mile standard would
(LDV) & Light light-duty
trucks (LLDT) ........................
0.3 apply for vehicles over 6000 lbs GVWR,
> 6000 lbs: Heavy light-duty
which includes both HLDTs (6000 lbs to
trucks (HLDT) up to 8,500
8500 lbs) and MDPVs.
lbs & Medium-duty pasWe are proposing the sales-weighted
senger vehicles (MDPV) up
fleet average approach because it
to 10,000 lbs .........................
0.5
achieves the greatest degree of emission
control feasible for Tier 2 vehicles,
We are proposing two separate saleswhile allowing manufacturers flexibility
weighted fleet average NMHC levels: (1)
to certify different vehicle groups to
0.3 g/mile for vehicles at or below 6,000
different levels and thus providing both
pounds GVWR and (2) 0.5 g/mile for
lower cost and feasible lead times. We
vehicles over 6,000 pounds, including
believe this is an appropriate approach
MDPVs.186 The new standard would not
because the base Tier 2 program is also
require additional certification testing
based on emissions averaging, and will
beyond what is required today with
result in a mix of emissions control
‘‘worst case’’ model selection of a
strategies across the fleet that would
durability test group.187 NMHC
have varying cold temperature
emissions would be measured during
capabilities. These capabilities won’t be
fully understood until manufacturers go
186 Tier 2 created the medium-duty passenger
through the process of evaluating each
vehicle (MDPV) category to include larger complete
Tier 2 package for cold temperature
passenger vehicles, such as SUVs and vans, with a
emissions control potential. Also, Tier 2
GVWR of 8,501–10,000 pounds GVWR. Large pickups above 8,500 pounds are not included in the
is still being phased in and some Tier
MDPV category but are included in the heavy-duty
2 vehicle emissions control packages are
vehicle category.
still being developed. A fleet average
187 The existing cold FTP test procedures are
provides manufacturers with flexibility
specified in 40 CFR Subpart C. In the proposed rule
for fuel economy labeling, recently signed on
to balance challenging vehicle families
January 10, 2006 (71, FR 5426, February 1, 2006),
with ones that more easily achieve the
EPA is seeking comment on the issue of requiring
standards.
manufacturers to run the heater and/or defroster
while conducting the cold FTP test. As discussed
in the fuel economy labeling proposed rule, we do
not believe this requirement would have a
significant impact on emissions.
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188 40 CFR Subpart C, § 86.244–94 requires the
measurement of all pollutants measured over the
FTP except NOX.
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There are several ways fleet averaging
can work. In Tier 2, we established bins
of standards to which individual vehicle
families were certified. Each bin
contains a NOX standard, and these NOX
standards are then sales-weighted to
demonstrate compliance with the
corporate average NOX standard. In
other emissions control programs, such
as the highway motorcycle program and
the highway and nonroad heavy-duty
engine programs, we have established a
Family Emissions Limit (FEL) structure.
In this approach, manufacturers
establish individual FELs for each group
of vehicles certified. These FELs serve
as the standard for each individual
group, and the FELs are averaged
together on a sales-weighted basis to
demonstrate overall compliance with
the standards. For the proposed new
cold temperature NMHC standards, we
are proposing to use the FEL-based
approach. We believe the FEL approach
adds flexibility and should lead to costeffective improvements in vehicle
emissions performance. The FEL
approach is discussed further in Section
VI.B.4 below.
We are proposing to apply the new
cold temperature NMHC standards to
Tier 2 gasoline-fueled vehicles. We are
not proposing to apply the standards to
diesel vehicles, alternative-fueled
vehicles, or heavy-duty vehicles, in
general, due to a lack of data on which
to base standards. Section VI.B., below,
provides a detailed discussion of
applicability.
As discussed above, we are expecting
PM reductions at cold temperatures as
a result of the control strategies we
expect manufacturers to meet under the
proposed cold temperature NMHC
standards. We may consider the need
for a separate PM standard under CAA
section 202(a), as part of a future
rulemaking, to further ensure that PM
reductions occur under cold
temperature conditions. We also request
comments on what testing challenges
exist for testing PM under cold
conditions. We request that comments
be supported by data where possible.
We request comments on the level of
the new standards and the averaging
approach we are proposing, and we urge
commenters to include supporting
information and data where possible.
2. Feasibility of the Proposed Standards
We believe the proposed standards
are feasible, based on our analysis of the
stringency of the standard provided
below and the lead time and flexibilities
described in section VI.B.3. We believe
that the proposed standards could be
achieved using a number of the
technologies discussed in the following
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section, but that none of these potential
technologies performs markedly better
than any other. Moreover, as explained
in section VI.D, we do not believe that
additional reductions would be feasible
without significant changes in Tier 2
technology, and we are not yet in a
position to fully evaluate the
achievability of standards based on such
technologies. We thus are not
considering more stringent cold
temperature NMHC standards. We
request comment on our analysis of the
feasibility of the proposed standards.
a. Currently Available Emission Control
Technologies
We believe that the cold temperature
NMHC standards being proposed today
for gasoline-fueled vehicles are
challenging but within the reach of Tier
2 level emission control technologies.
Our proposed determination of
feasibility is based on the emission
control hardware and strategies that are
already in use today on Tier 2 vehicles.
These emission control technologies are
successfully used to meet the stringent
Tier 2 standards for HC at the FTP
temperature range of 68° F to 86° F, but
generally are not fully used or activated
at colder temperatures. As discussed in
section VI.D, we are not proposing
standards that would force changes to
Tier 2 technology at this time. As
discussed above, many current engine
families are already achieving emissions
levels at or below the proposed
emission standards (see RIA Chapter 5),
while other engine families are at levels
greater than twice the proposed
standard. The only apparent reason for
the difference is the failure of some
vehicles to use the Tier 2 control
technologies at cold temperatures.
While manufacturers could always
choose to use additional hardware to
facilitate compliance with the proposed
standard, many of the engine families
already at levels below the proposed
standard do not necessarily contain any
unique enabling hardware. These
vehicles appear to achieve their results
through mainly software and calibration
control technologies. Thus, we believe
our proposed standards can be met by
the application of calibration and
software approaches similar to those
currently used at 50° F and 75° F, and
we have estimated cost of control based
on use of calibration and software
approaches. Estimated costs are
provided in section IX below, and in
Chapter 8 of the RIA. As described in
section VI.B.2.c, our own feasibility
testing of a vehicle over 6000 lbs GVWR
achieved NMHC reductions consistent
with the proposed standard without the
use of new hardware.
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In addition, a 20° F cold hydrocarbon
requirement has been in place in Europe
since approximately the 2002 model
year.189 Many manufacturers currently
have common vehicle models offered in
Europe and the U.S. market. While the
European standard is over a different
drive cycle, unique strategies have been
developed to comply with this standard.
In fact, when the new European cold
hydrocarbon standard was implemented
in conjunction with a new 75° F
standard (Euro4), many manufacturers
responded by implementing NLEV level
hardware and supplementing this
hardware with advanced cold start
emission control strategies. Although
we are proposing a sales-weighted fleet
average standard, the European standard
is a fixed standard that cannot be
exceeded by any vehicle model. Like the
standard we are proposing, Europe also
has made distinctions in the level of the
standard reflecting that heavier weight
vehicles cannot achieve as stringent a
standard. Those manufacturers with
European models shared with the U.S.
market have the opportunity to leverage
their European models or divisions in
an attempt to transfer the emission
control technologies that are used today
for 20° F hydrocarbon control.
There are several different approaches
or strategies used in the vehicles that are
achieving proportional improvements in
NMHC emissions at 20° F FTP. Several
European models sold in the U.S.
market that demonstrate excellent cold
hydrocarbon performance are utilizing
secondary air systems at the 20° F start
temperature. These secondary air
systems, sometimes called air pumps,
inject ambient air into the exhaust
immediately after the cold start. This
performs additional combustion of
unburned hydrocarbons prior to the
catalytic converter and also accelerates
the necessary heating of the catalytic
converter. In the past and even recently,
these systems have been used
extensively to improve hydrocarbon
performance at 75° F starts. As
predicted in the Tier 2 Final Rule, a
portion of the Tier 2 fleet is being
equipped with secondary air systems in
order to comply with Tier 2 standards.
Some manufacturers that currently
have these systems available on their
vehicles have indicated that they are
simply not utilizing them at
temperatures below freezing due to past
engineering issues. The manufacturers
that are using secondary air at 20° F,
mainly European manufacturers, have
indicated that these engineering
189 European Union (EU) Type VI Test (¥7° C)
required for new vehicle model certified as of 1/1/
2002.
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challenges have been addressed through
design changes. The robustness of these
systems below freezing has also been
confirmed with the manufacturers and
with the suppliers of the secondary air
components.190 While not necessarily
producing 20° F NMHC emission results
better than other available technologies,
vehicles equipped with this technology
should be able to meet the proposed 20°
F standard by capitalizing on this
hardware.
Manufacturers have also used several
other strategies to successfully produce
proportional improvements in
hydrocarbon emissions at 20° F. These
include lean limit fuel strategies,
elevated idle speeds, retarded spark
timing, and accelerated closed loop
times. Some software design strategies
include fuel injection strategies detailed
in past Society of Automotive Engineers
(SAE) papers 191 that synchronize fuel
injection timing with engine intake
valve position to provide optimal fuel
preparation. Spark delivery strategies
have also been entertained that include
higher energy levels and even
redundant spark delivery to possibly
complete additional combustion of
unburned hydrocarbons. We expect that
software and/or calibration changes,
such as previously described, will
generally perform as well or better than
added hardware. This is because critical
hardware such as the catalyst may not
be immediately usable directly
following the cold start. See RIA
Chapter 5 for further discussion.
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b. Feasibility Considering Current
Certification Levels, Deterioration and
Compliance Margin
Of the vehicles that were certified to
Tier 2 and demonstrated proportional
improvements in hydrocarbon
emissions, approximately 20% of
vehicles below 6,000 pounds GVWR
had certification levels in the range of
two to three times the 75° F Tier 2 bin
5 full useful life standard (.18 g/mile to
.27 g/mile). These reported hydrocarbon
levels are from Cold CO test results for
certification test vehicles with typically
only 4,000 mile aged systems, without
full useful life deterioration applied.
Due to rapid advances in emission
control hardware technology,
deterioration factors used today by
manufacturers to demonstrate full
useful life compliance are very low and
190 Memo to docket ‘‘Discussions Regarding
Secondary Air System Usage at 20° F with
European Automotive Manufacturers and Suppliers
of Secondary Air Systems,’’ December 2005.
191 Meyer, Robert and John B. Heywood, ‘‘Liquid
Fuel Transport Mechanisms into the Cylinder of a
Firing Port-Injected SI Engine During Start-up,’’
SAE 970865, 1997.
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typically even indicate little or no
deterioration over the life of the vehicle.
The deterioration factors generated
today by manufacturers are common
across all required test cycles including
cold temperature testing. The standards
we are proposing will have a full useful
life of 120,000 miles, consistent with
Tier 2 standards. Additionally,
manufacturers typically target
certification emission levels that
incorporate a 20% to 30% compliance
margin primarily to account for in-use
issues that may cause emissions
variability. The 0.3 g/mile FEL standard
would leave adequate flexibility for
compliance margins and any emissions
deterioration concerns. See RIA Chapter
5 for further discussion and details
regarding current certification levels.
Given enough lead time, we believe
manufacturers would be able to develop
control strategies for each of their
widely varying product lines utilizing
the approaches outlined above without
fundamentally changing the design of
the vehicles.
lead time and flexibility within the
program structure, which also
contribute to the feasibility of the
proposed standards. Chapter 8 of the
RIA provides our cost estimations per
vehicle and on a nationwide basis,
including capital and development
costs. We believe the estimated costs are
reasonable and the proposal is cost
effective, as provided in section IX,
below. Given the emission control
strategies we expect manufacturers to
utilize, we expect feasible
implementation of technologies without
a significant impact on vehicle noise,
energy consumption, or safety factors.
Although manufacturers would need to
employ new emissions control strategies
at cold temperatures, fundamental Tier
2 vehicle hardware and designs are not
expected to change. In addition, we are
providing necessary lead time for
manufacturers to identify and resolve
any related issues as part of overall
vehicle development. We request
comment on our analysis of the
feasibility of the proposed standards.
c. Feasibility and Test Programs for
Higher Weight Vehicles
While a few of the heavier vehicles
achieved a standard similar to the
lighter weight class, there were limited
certification results available for Tier 2
compliant vehicles over 6000 lbs GVWR
(due to the later Tier 2 phase-in
schedule for these vehicles). To further
support the feasibility of the standard
for heavier vehicles, we conducted a
feasibility study for Tier 2 vehicles over
6000 lbs GVWR to assess their
capabilities with typical Tier 2
hardware. We were able to reduce HC
emissions for one vehicle with models
above and below 6,000 pounds GVWR
by between 60–70 percent, depending
on control strategy, from a baseline level
of about 1.0 g/mile. The results are well
within the 0.5 g/mile standard including
compliance margin, and we even
achieved a 0.3 g/mile level on some
tests. We achieved these reductions
through recalibration without the use of
new hardware. The findings from the
study are provided in detail in the RIA.
We believe the proposed standards
are feasible while at the same time
providing the greatest degree of
emission reduction achievable through
the application of available technology.
Our feasibility assessment, provided
above, is based on our analysis of the
stringency of the standard given current
emission levels at certification
(considering deterioration, compliance
margin, and vehicle weight); available
emission control techniques; and our
own feasibility testing. In addition,
sections VI.B.3–6 describe the proposed
3. Standards Timing and Phase-in
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a. Phase-In Schedule
EPA must consider lead time in
determining the greatest degree of
emission reduction achievable under
section 202(l) of the CAA. We are
proposing to begin implementing the
standard in the 2010 model year (MY)
for LDVs/LLDTs and 2012 MY for
HLDTs/MDPVs. The proposed
implementation schedule, in Table
VI.B–2, begins 3 model years after Tier
2 phase-in is complete for both vehicle
classes. Manufacturers would
demonstrate compliance with phase-in
requirements through sales projections,
similar to Tier 2. The 3-year period
between completion of the Tier 2 phasein and the start of the new cold NMHC
standard should provide vehicle
manufacturers sufficient lead time to
design their compliance strategies and
determine the product development
plans necessary to meet the new
standards. We believe that this phase-in
schedule is needed to allow
manufacturers to develop compliant
vehicles without significant disruptions
in the product development cycles.
Also, for vehicles above 6,000 GVWR,
section 202(a) of the Act requires that
four years of lead time be provided to
manufacturers.
We recognize that the new cold
temperature standards we are proposing
could represent a significant new
challenge for manufacturers and
development time will be needed. The
issue of NMHC control at cold
temperatures was not anticipated by
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many entities, and research and
development to address the issue is
consequently at a rudimentary stage.
Lead time is therefore necessary before
compliance can be demonstrated. While
certification will only require one
vehicle model of a durability group to
be tested, manufacturers must do
development on all vehicle
combinations to ensure full compliance
15849
within the durability test group. We
believe a phase-in allows the program to
begin sooner than would otherwise be
feasible.
TABLE VI.B–2.—PROPOSED PHASE-IN SCHEDULE FOR 20 °F NMHC STANDARD BY MODEL YEAR
2010
2011
≤ 6000 lbs (LDV/LLDT) ....................................................
> 6000 lbs HLDT and MDPV ...........................................
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Vehicle GVWR (category)
25%
....................
50%
....................
In considering a phase-in period,
manufacturers have raised concerns that
a rapid phase-in schedule would lead to
a significant increase in the demand for
their cold testing facilities, which could
necessitate substantial capital
investment in new cold test facilities to
meet development needs. This is
because manufacturers would need to
use their cold testing facilities not only
for certification but also for vehicle
development. If vehicle development is
compressed into a narrow time window,
significant numbers of new facilities
would be needed. Manufacturers were
further concerned that investment in
new test facilities would be stranded at
the completion of the initial
development and phase-in period.
As stated earlier, durability test
groups may be large and diverse and
therefore require significant
development effort and cold test facility
usage for each model. Our proposed
phase-in period accommodates test
facilities and work load concerns by
distributing these fleet phase-in
percentage requirements over a 4-year
period for each vehicle weight category.
The staggered start dates for the phasein schedule between the two weight
categories should further alleviate
manufacturers’ concerns with needing
to construct new test facilities. Some
manufacturers may still determine that
upgrades to their current cold facility
are needed to handle increased
workload. Some manufacturers have
indicated that they would simply add
additional shifts to their facility work
schedules that are not in place today.
Some manufacturers will already meet
the first-year requirement based on
current certification reporting,
essentially providing an additional year
for distributing the anticipated
development test burden for the
remaining fleet. The 4-year phase-in
period provides ample time for vehicle
manufacturers to develop a compliance
schedule that is coordinated with their
future product plans and projected
product sales volumes of the different
vehicle models.
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2012
We request comments on the
proposed start date and duration of the
phase-in schedule. We also request
comment on allowing a volume-based
offset during the phase-in period for
cases where manufacturers voluntarily
certify heavy-duty vehicles above 8,500
pound GVWR to the proposed cold
temperature standards. This may
provide incentive for voluntary
certification of these heavier vehicles.
b. Alternative Phase-In Schedules
Alternative phase-in schedules
essentially credit the manufacturer for
its early or accelerated efforts and allow
the manufacturer greater flexibility in
subsequent years during the phase-in.
By introducing vehicles earlier than
required, manufacturers would earn the
flexibility to make offsetting
adjustments, on a vehicle-year basis, to
the phase-in percentages in later years.
Under these alternative schedules,
manufacturers would have to introduce
vehicles that meet or surpass the NHMC
average standards before they are
required to do so, or else introduce
vehicles that meet or surpass the
standard in greater quantities than
required.
We are proposing that manufacturers
may apply for an alternative phase-in
schedule that would still result in 100%
phase-in by 2013 and 2015,
respectively, for the lighter and heavier
weight categories. As with the primary
phase-in, manufacturers would base an
alternative phase-in on their projected
sales estimates. An alternate phase-in
schedule submitted by a manufacturer
would be subject to EPA approval and
would need to provide the same
emissions reductions as the primary
phase-in schedule. We propose that the
alternative phase-in could not be used
to delay full implementation past the
last year of the primary phase-in
schedule (2013 for LDVs/LDTs and 2015
for HLDTs/MDPVs).
An alternative phase-in schedule
would be acceptable if it passes a
specific mathematical test. We have
designed the test to provide
manufacturers a benefit from certifying
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2013
75%
25%
100%
50%
2014
2015
....................
75%
....................
100%
to the standards early, while ensuring
that significant numbers of vehicles are
introduced during each year of the
alternative phase-in schedule.
Manufacturers would multiply their
percent phase-in by the number of years
the vehicles are phased in prior to the
second full phase-in year. The sum of
the calculation would need to be greater
than or equal to 500, which is the sum
from the primary phase-in schedule
(4*25 + 3*50 + 2*75 + 1*100=500). For
example, the equation for LDVs/LLDTs
would be as follows:
(6×API2008) + (5×API 2009) + (4×API 2010)
+ (3×API 2011) + (2×API 2012) +
(1×API 2013) ≥ 500%,
Where:
API is the anticipated phase-in
percentage for the referenced model
year.
California used this approach to an
alternative phase-in for the LEVII
program.192 It provides alternative
phase-in credit for both the number of
vehicles phased in early and the number
of years the early phase-in occurs.
As described above, the final sum of
percentages for both LDVs/LDTs and
HLDTs/MDPVs must equal or exceed
500—the sum that results from a 25/50/
75/100 percent phase-in. For example, a
10/25/50/55/100 percent phase-in for
LDVs/LDTs that begins in 2009 will
have a sum of 510 percent and is
acceptable. A 10/20/40/70/100 percent
phase-in that begins the same year has
a sum of 490 percent and is not
acceptable.
To ensure that significant numbers of
LDVs/LDTs are introduced in the 2010
time frame (2012 for HLDTs/MDPVs),
manufacturers would not be permitted
to use alternative phase-in schedules
that delay the implementation of the
requirements, even if the sum of the
phase-in percentages ultimately meets
or exceeds 500. Such a situation could
occur if a manufacturer delayed
implementation of its compliant
production until 2011 and began an 80/
85/100 percent phase-in that year for
192 Title 13, California Code of Regulations,
Section 1961(b)(2).
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LDVs/LDTs. To protect against this
possibility, we are proposing that for
any alternative phase-in schedule, a
manufacturer’s phase-in
percentages*years factor from the 2010
and earlier model years sum to at least
100 (2012 and earlier for HLDTs/
MDPVs). The early phase-in also
encourages the early introduction of
vehicles meeting the new standard or
the introduction of such vehicles in
greater quantity than required. This
would achieve early emissions
reductions and provide an opportunity
to gain experience in meeting the
standards.
Phase-in schedules, in general, add
little flexibility for manufacturers with
limited product offerings because a
manufacturer with only one or two test
groups cannot take full advantage of a
25/50/75/100 percent or similar phasein. Therefore, consistent with the
recommendations of the Small
Advocacy Review Panel (SBAR Panel),
which we discuss in more detail later in
section VI.E, manufacturers meeting
EPA’s definition of ‘‘small volume
manufacturer’’ would be exempt from
the phase-in schedules and would be
required to simply comply with the
final 100% compliance requirement.
This provision would only apply to
small volume manufacturers and not to
small test groups of larger
manufacturers.
4. Certification Levels
Manufacturers typically certify
groupings of vehicles called durability
groups and test groups, and they have
some discretion on what vehicle models
are placed in each group. A durability
group is the basic classification used by
manufacturers to group vehicles to
demonstrate durability and predict
deterioration. A test group is a basic
classification within a durability group
used to demonstrate compliance with
FTP 75° F standards.193 For Cold CO,
manufacturers certify on a durability
group basis, whereas for 75° F FTP
testing, manufacturers certify on a test
group basis. In keeping with the current
cold CO standards, we are proposing to
require testing on a durability group
basis for the cold temperature NMHC
standard. We also propose to allow
manufacturers the option of certifying
on the smaller test group basis, as is
allowed under current cold CO
standards. Testing on a test group basis
would require more tests to be run by
manufacturers but may provide them
with more flexibility within the
averaging program. In either case, the
worst case vehicle within the group
193 40
CFR 86.1803–01.
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from an NMHC emissions standpoint
would be tested for certification.
For the new standard, manufacturers
would declare a family emission limit
(FEL) for each group either at, above, or
below the fleet averaging standard. The
FEL would be based on the certification
NMHC level, including deterioration
factor, plus the compliance margin
manufacturers feel is needed to ensure
in-use compliance. The FEL becomes
the standard for each group, and each
group could have a different FEL so long
as the projected sales-weighted average
level met the fleet average standard at
time of certification. Like the standard,
the certification resolution for the FEL
would be one decimal point. This FEL
approach would be similar to having
bins in 0.1 g/mile intervals, with no
upper limit. Similar to a bin approach,
manufacturers would compute a salesweighted average for the NMHC
emissions at the end of the model year
and then determine credits generated or
needed based on how much the average
is above or below the standard.
5. Credit Program
As described above, we are proposing
that manufacturers average the NMHC
emissions of their vehicles and comply
with a corporate average NMHC
standard. In addition, we are proposing
that when a manufacturer’s average
NMHC emissions of vehicles certified
and sold falls below the corporate
average standard, it could generate
credits that it could save for later use
(banking) or sell to another
manufacturer (trading). Manufacturers
would consume any credits if their
corporate average NMHC emissions
were above the applicable standard for
the weight class.
EPA views the proposed averaging,
banking, and trading (ABT) provisions
as an important element in setting
emission standards reflecting the
greatest degree of emission reduction
achievable, considering factors
including cost and lead time. If there are
vehicles that will be particularly costly
or have a particularly hard time coming
into compliance with the standard, a
manufacturer can adjust the compliance
schedule accordingly, without special
delays or exceptions having to be
written into the rule. This is an
important flexibility especially given
the current uncertainty regarding
optimal technology strategies for any
given vehicle line. In addition, ABT
allows us to consider a more stringent
emission standard than might otherwise
be achievable under the CAA, since
ABT reduces the cost and improves the
technological feasibility of achieving the
standard. By enhancing the
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technological feasibility and cost
effectiveness of the proposed standard,
ABT allows the standard to be attainable
earlier than might otherwise be possible.
Credits may be generated prior to,
during, and after the phase-in period.
Manufacturers could certify LDVs/
LLDTs to standards as early as the 2008
model year (2010 for HLDTs/MDPVs)
and receive early NMHC credits for their
efforts. They could use credits generated
under these ‘‘early banking’’ provisions
after the phase-in begins in 2010 (2012
for HLDTs/MDPVs).
a. How Credits Are Calculated
The corporate average for each weight
class would be calculated by computing
a sales-weighted average of the NMHC
levels to which each FEL was certified.
As discussed above, manufacturers
group vehicles into durability groups or
test groups and establish an FEL for
each group. This FEL becomes the
standard for that group. Consistent with
FEL practices in other programs,
manufacturers may opt to select an FEL
above the test level. The FEL would be
used in calculating credits. The number
of credits or debits would then be
determined using the following
equation:
Credits or Debits = (Standard ¥ Sales
weighted average of FELs to nearest
tenth) × Actual Sales
If a manufacturer’s average was below
the 0.3 g/mi corporate average standard
for LDVs/LDTs, credits would be
generated (below 0.5 g/mi for HLDTs/
MDPVs). These credits could then be
used in a future model year when its
average NMHC might exceed the 0.3 or
the 0.5 standard. Conversely, if the
manufacturer’s fleet average was above
the corporate average standard, banked
credits could offset the difference, or
credits could be purchased from another
manufacturer.
b. Credits Earned Prior to Primary
Phase-in Schedule
We propose that manufacturers could
earn early emissions credits if they
introduce vehicles that comply with the
new standards early and the corporate
average of those vehicles is below the
applicable standard. Early credits could
be earned starting in 2008 for vehicles
meeting the 0.3 g/mile standard and in
2010 for vehicles meeting the 0.5 g/mile
standard. These emissions credits
generated prior to the start of the phasein could be used both during and after
the phase-in period and have all the
same properties as credits generated by
vehicles subject to the primary phase-in
schedule. As previously mentioned, we
are also proposing that manufacturers
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may apply for an alternative phase-in
schedule for vehicles that are
introduced early. The alternative phasein and early credits provisions would
operate independent of one another.
c. How Credits Can Be Used
A manufacturer could use credits in
any future year when its corporate
average was above the standard, or it
could trade (sell) the credits to other
manufacturers. Because of separate sets
of standards for the different weight
categories, we are proposing that
manufacturers compute their corporate
NMHC averages separately for LDV/
LLDTs and HLDTs/MDPVs. Credit
exchanges between LDVs/LLDTs and
HLDTs/MDPVs would be allowed. This
will provide added flexibility for fullerline manufacturers who may have the
greatest challenge in meeting the new
standards due to their wide disparity of
vehicle types/weights and emissions
levels.
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d. Discounting and Unlimited Life
Credits would allow manufacturers a
way to address unexpected shifts in
their sales mix. The NMHC emission
standards in this proposed program are
quite stringent and do not present easy
opportunities to generate credits.
Therefore, we are not proposing to
discount unused credits. Further, the
degree to which manufacturers invest
the resources to achieve extra NMHC
reductions provides true value to the
manufacturer and the environment. We
do not want to take measures to reduce
the incentive for manufacturers to bank
credits, nor do we want to take
measures to encourage unnecessary
credit use. Consequently we are not
proposing that the NMHC credits would
have a credit life limit. However, we are
proposing that they only be used to
offset deficits accrued with respect to
the proposed 0.3/0.5 g/mile cold
temperature standards. We request
comment on the need for discounting of
credits or credit life limits and what
those discount rates or limits, if any,
should be.
e. Deficits Could Be Carried Forward
When a manufacturer has an NMHC
deficit at the end of a model year—that
is, its corporate average NMHC level is
above the required corporate average
NMHC standard—we are proposing that
the manufacturer be allowed to carry
that deficit forward into the next model
year. Such a carry-forward could only
occur after the manufacturer used any
banked credits. If the deficit still existed
and the manufacturer chose not to, or
was unable to, purchase credits, the
deficit could be carried over. At the end
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of that next model year, the deficit
would need to be covered with an
appropriate number of credits that the
manufacturer generated or purchased.
Any remaining deficit would be subject
to an enforcement action.
To prevent deficits from being carried
forward indefinitely, we propose that
manufacturers would not be permitted
to run a deficit for two years in a row.
We believe that it is reasonable to
provide this flexibility to carry a deficit
for one year given the uncertainties that
manufacturers face with changing
market forces and consumer
preferences, especially during the
introduction of new technologies. These
uncertainties can make it hard for
manufacturers to accurately predict
sales trends of different vehicle models.
f. Voluntary Heavy-Duty Vehicle Credit
Program
In addition to MDPV requirements in
Tier 2, we also currently have chassisbased emissions standards for other
complete heavy-duty vehicles (e.g., large
pick-ups and cargo vans) above 8,500
pound GVWR. However, these
standards do not include cold
temperature CO standards. As noted
below in section VI.B.6.a, we are not
proposing to apply cold temperature
NMHC standards to heavy-duty gasoline
vehicles due to a current lack of
emissions data on which to base such
standards. We plan to revisit the need
for and feasibility of standards as data
become available.
During discussions with
manufacturers, we discussed a
voluntary program for chassis-certified
complete heavy-duty vehicles. We
believe that there may be opportunities
within the framework of a cold
temperature NMHC program to allow for
emissions credits from chassis-certified
heavy-duty vehicles above 8,500 pounds
GVWR to be used to meet the proposed
standards. It is possible that some
control strategies developed for meeting
cold NMHC emissions standards could
also be applied to these vehicles above
8,500 pounds GVWR.
One approach would be to allow
manufacturers to certify heavy-duty
vehicles voluntarily to the 0.5 g/mile
cold NMHC standards proposed for
HLDTs/MDPVs. To the extent that
heavy-duty vehicles achieve FELs below
the 0.5 g/mile standard, manufacturers
could earn credits which could be
applied to any vehicle subject to the
proposed standard. It is unclear,
however, if this approach would
provide a meaningful opportunity for
credit generation, given the stringency
of the standard. We would expect that
most heavy-duty vehicles would have
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15851
emissions well above the 0.5 g/mile
level, based on the additional weight of
the vehicle. We request comment on
this approach, as well as others for
voluntary certification and credit
generation.
It may be possible to establish a
voluntary standard above 0.5 g/mile for
purposes of generating credits, but we
would need data on which to base this
level of the standard. Suggestions on an
appropriate level of a voluntary
standard are welcomed, as well as any
data that support such a
recommendation. Comments on testing
protocols, such as use of the vehicle’s
adjusted loaded vehicle weight (ALVW)
or loaded vehicle weight (LVW), are also
encouraged. We believe such a
voluntary program could provide
significant data that would help us
evaluate the feasibility of a future
standard for these vehicles.
6. Additional Vehicle Cold Temperature
Standard Provisions
We request comments on all of the
following proposed provisions.
a. Applicability
We are proposing to apply the new
cold temperature standards to all
gasoline-fueled light-duty vehicles and
MDPVs sold nationwide. While we have
significant amounts of data on which to
base our proposals for gasoline-fueled
light-duty vehicles, we have very little
data for light-duty diesels. For 75° F
FTP standards, the same set of standards
apply, but in the 20° F context we know
very little about diesel emissions due to
a lack of data. Currently, diesel vehicles
are not subject to the cold CO standard,
so there are no requirements to test
diesel vehicles at cold temperatures.
There are sound engineering reasons,
however, to expect cold NMHC
emissions for diesel vehicles to be as
low as or even lower than the proposed
standards. This is because diesel
engines operate under leaner air-fuel
mixtures compared to gasoline engines,
and therefore have fewer engine-out
NMHC emissions due to the abundance
of oxygen and more complete
combustion. A very limited amount of
confidential manufacturer-furnished
information is consistent with this
engineering hypothesis. A
comprehensive assessment of
appropriate standards for diesel vehicles
would require a significant amount of
investigation and analysis of issues such
as feasibility and costs. This effort
would be better suited to a future
rulemaking. Therefore, at this time, we
are not proposing to apply the cold
NMHC standards to light-duty diesel
vehicles. We will continue to evaluate
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data for these vehicles as they enter the
fleet and will reconsider the need for
standards if data indicate that there may
be instances of high NMHC emissions
from diesels at cold temperatures. We
have proposed cold temperature FTP
testing for diesels as part of the Fuel
Economy Labeling rulemaking,
including NMHC measurement.194 This
testing data would allow us to assess
NMHC certification type data over time.
However, this wouldn’t include
development testing manufacturers
would need to do in order to meet a new
diesel cold temperature standard.
In addition, there currently is no cold
CO testing requirement for alternative
fuel vehicles. There are little data upon
which to evaluate NMHC emissions
when operating on alternative fuels at
cold temperatures. For fuels such as
ethanol, it is difficult to develop a
reasonable proposal due to a lack of fuel
specifications, testing protocols, and
current test data. Other fuels such as
methanol and natural gas pose similar
uncertainty. Therefore, we are not
proposing a cold NMHC testing
requirement for alternative fuel
vehicles. We will continue to investigate
these other technologies and request
comment on standards for vehicles
operating on fuels other than gasoline.
We are proposing that flex-fuel
vehicles would still require certification
to the applicable cold NMHC standard,
though only when operated on gasoline.
For multi-fuel vehicles, manufacturers
would need to submit a statement at the
time of certification that either confirms
the same control strategies used with
gasoline would be used when operating
on ethanol, or that identifies any
differences as an Auxiliary Emission
Control Device (AECD). Again,
dedicated alternative-fueled vehicles,
including E–85 vehicles, would not be
covered.
For heavy-duty gasoline-fueled
vehicles, we have no data, but we would
expect a range of emissions performance
similar to that of lighter gasoline-fueled
trucks. Due to the lack of test data on
which to base feasibility and cost
analyses, we are not proposing cold
temperature NMHC standards for these
vehicles at this time. We request
comments and data on these vehicles
and plan to revisit this issue when
sufficient data is available.
emission data for EPA evaluation to
quantify any emission impact and
validity of the AECD.
b. Useful Life
The ‘‘useful life’’ of a vehicle means
the period of use or time during which
an emission standard applies to lightduty vehicles and light-duty trucks.195
Consistent with the current definition of
useful life in the Tier 2 regulations, for
all LDVs/LDTs and HLDTs/MDPVs, we
are proposing new full useful life
standards for cold temperature NMHC
standards. Given that we expect that
manufacturers will make calibration or
software changes to existing Tier 2
technologies, it is reasonable for there to
be the same useful life as for the Tier 2
standards themselves. For LDV/LLDT,
the full useful life values would be
120,000 miles or 10 years, whichever
comes first, and for HLDT/MDPV, full
useful life is 120,000 miles or 11 years,
whichever comes first.196
As we have indicated, the standards
we are proposing would be more
challenging for some vehicles than for
others. With any new technology, or
even with new calibrations of existing
technology, there are risks of in-use
compliance problems that may not
appear in the certification process. Inuse compliance concerns may
discourage manufacturers from applying
new calibrations or technologies. Thus,
it may be appropriate for the first few
years, for those vehicles most likely to
require the greatest applications of
effort, to provide assurance to the
manufacturers that they will not face
recall if they exceed standards in use by
a specified amount. Therefore, similar to
the approach used in Tier 2, we are
proposing an in-use standard that is 0.1
g/mile higher than the certification FEL
for any given test group for a limited
number of model years.197 For example,
a test group with a 0.2 g/mile FEL
would have an in-use standard of 0.3 g/
mile. This would not change the FEL or
averaging approaches and would only
apply in cases where EPA tests vehicles
in-use to ensure emissions compliance.
We propose that the in-use standards
be available for the first few model years
of sales after a test group meeting the
new standards is introduced, according
to a schedule that provides more years
for test groups introduced earlier in the
phase-in. This schedule provides
manufacturers with time to determine
the in-use performance of vehicles and
learn from the earliest years of the
program to help ensure that vehicles
introduced after the phase-in period
meet the final standards in-use. It also
assumes that once a test group is
certified to the new standards, it will be
carried over to future model years. The
tables below provide the proposed
schedule for the availability of the inuse standards.
c. High Altitude
We do not expect emissions to be
significantly different at high altitude
due to the use of common emissions
control calibrations. Limited data
submitted by a manufacturer suggest
that FTP emissions performance at high
altitude generally follows sea level
performance. Furthermore, there are
very limited cold temperature testing
facilities at high altitudes. Therefore,
under normal circumstances,
manufacturers would not be required to
submit vehicle test data for high
altitude. Instead, manufacturers would
be required to submit an engineering
evaluation indicating that common
calibration approaches are utilized at
high altitude. Any deviation from sea
level in emissions control practices
would be required to be included in the
auxiliary emission control device
(AECD) descriptions submitted by
manufacturers at certification.
Additionally, any AECD specific to high
altitude would require engineering
d. In-Use Standards for Vehicles
Produced During Phase-In
TABLE VI.B–3.—SCHEDULE FOR IN-USE STANDARDS FOR LDVS/LLDTS
Model year of introduction
2008
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Models years that the in-use standard is available for carry-over test
groups ...................................................................................................
194 ‘‘Fuel Economy Labeling of Motor Vehicles;
Revisions to Improve Calculation of Fuel Economy
Estimates,’’ Proposed Rule, 71, FR 5426, February
1, 2006.
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196 40
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CFR 86.1805–04.
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197 ‘‘Control of Air Pollution from New Motor
Vehicles: Tier 2 Motor Vehicle Emissions Standards
and Gasoline Sulfur Control Requirements’’, Final
Rule, 65 FR 6796, February 10, 2000.
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TABLE VI.B–4.—SCHEDULE FOR IN-USE STANDARDS FOR HLDVS/MDPVS
Model year of introduction
2010
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Models years that the in-use standard is available for carry-over test
groups.
7. Monitoring and Enforcement
Under the proposed programs,
manufacturers could either report that
they met the relevant corporate average
standard in their annual reports to the
Agency, or they could show via the use
of credits that they have offset any
exceedance of the corporate average
standard. Manufacturers would also
report their credit balances or deficits.
EPA would monitor the program.
As in Tier 2, the averaging, banking
and trading program would be enforced
through the certificate of conformity
that manufacturers must obtain in order
to introduce any regulated vehicles into
commerce.198 The certificate for each
test group would require all vehicles to
meet the emissions level to which the
vehicles were certified, and would be
conditioned upon the manufacturer
meeting the corporate average standard
within the required time frame. If a
manufacturer failed to meet this
condition, the vehicles causing the
corporate average exceedance would be
considered to be not covered by the
certificate of conformity for that engine
family. A manufacturer would be
subject to penalties on an individual
vehicle basis for sale of vehicles not
covered by a certificate.
EPA would review the manufacturer’s
sales to designate the vehicles that
caused the exceedance of the corporate
average standard. We would designate
as nonconforming those vehicles in
those test groups with the highest
certification emission values first,
continuing until a number of vehicles
equal to the calculated number of
noncomplying vehicles as determined
above is reached. In a test group where
only a portion of vehicles would be
deemed nonconforming, we would
determine the actual nonconforming
vehicles by counting backwards from
the last vehicle produced in that test
group. Manufacturers would be liable
for penalties for each vehicle sold that
is not covered by a certificate.
We are proposing to condition
certificates to enforce the requirements
that manufacturers not sell credits that
198 ‘‘Control of Air Pollution from New Motor
Vehicles: Tier 2 Motor Vehicle Emissions Standards
and Gasoline Sulfur Control Requirements’’, Final
Rule, 65 FR 6797, February 10, 2000.
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2011
2012
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2012
2013
2014
they have not generated. A
manufacturer that transferred credits it
did not have would create an equivalent
number of debits that it would be
required to offset by the reporting
deadline for the same model year.
Failure to cover these debits with
credits by the reporting deadline would
be a violation of the conditions under
which EPA issued the certificate of
conformity, and nonconforming
vehicles would not be covered by the
certificate. EPA would identify the
nonconforming vehicles in the same
manner described above.
In the case of a trade that resulted in
a negative credit balance that a
manufacturer could not cover by the
reporting deadline for the model year in
which the trade occurred, we propose to
hold both the buyer and the seller liable.
We believe that holding both parties
liable will induce the buyer to exercise
diligence in assuring that the seller has
or will be able to generate appropriate
credits and will help to ensure that
inappropriate trades do not occur.
We are not proposing any new
compliance monitoring activities or
programs for vehicles. These vehicles
would be subject to the certification
testing provisions of the CAP2000 rule.
We are not proposing to require
manufacturer in-use testing to verify
compliance. There is no cold CO
manufacturer in-use testing requirement
today (similarly, we do not require
manufacturer in-use testing for SCO3
standards under the SFTP program). As
noted earlier, manufacturers have
limited cold temperature testing
capabilities and we believe these
facilities will be needed for product
development and certification testing.
However, we have the authority to
conduct our own in-use testing program
for exhaust emissions to ensure that
vehicles meet standards over their full
useful life. We will pursue remedial
actions when substantial numbers of
properly maintained and used vehicles
fail any standard in-use. We also retain
the right to conduct Selective
Enforcement Auditing of new vehicles
at manufacturers’ facilities.
The use of credits would not be
permitted to address Selective
Enforcement Auditing or in-use testing
failures. The enforcement of the
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averaging standard would occur through
the vehicle’s certificate of conformity. A
manufacturer’s certificate of conformity
would be conditioned upon compliance
with the averaging provisions. The
certificate would be void ab initio if a
manufacturer failed to meet the
corporate average standard and did not
obtain appropriate credits to cover their
shortfalls in that model year or in the
subsequent model year (see proposed
deficit carryforward provision in section
VI.B.5.e.). Manufacturers would need to
track their certification levels and sales
unless they produced only vehicles
certified to NMHC levels below the
standard and did not plan to bank
credits.
We request comments on the above
approach for compliance monitoring
and enforcement.
C. What Evaporative Emissions
Standards Are We Proposing?
We are proposing to adopt a set of
numerically more stringent evaporative
emission standards for all light-duty
vehicles, light-trucks, and medium-duty
passenger vehicles. The proposed
standards are equivalent to California’s
LEV II standards, and these proposed
standards are shown in Table VI.C–1.
The proposed standards would
represent about a 20 to 50 percent
reduction (depending on vehicle weight
class and type of test) in diurnal plus
hot soak standards from the Tier 2
standards that will be in effect in the
years immediately preceding the
implementation of today’s proposed
standards.199 As with the current Tier 2
evaporative emission standards, the
proposed standards vary by vehicle
weight class. The increasingly higher
standards for heavier weight class
vehicles account for larger vehicle sizes
199 Diurnal emissions (or diurnal breathing losses)
means evaporative emissions as a result of daily
temperature cycles or fluctuations for successive
days of parking in hot weather. Hot soak emissions
(or hot soak losses) are the evaporative emissions
from a parked vehicle immediately after turning off
the hot engine. For the evaporative emissions test
procedure, diurnal and hot soak emissions are
measured in an enclosure commonly called the
SHED (Sealed Housing for Evaporative
Determination).
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and fuel tanks (non-fuel and fuel
emissions).200
TABLE VI.C–1.—PROPOSED EVAPORATIVE EMISSION STANDARDS
[Grams of hydrocarbons per test]
3-day diurnal
plus hot soak
Vehicle class
LDVs ....................................................................................................................................................................
LLDTs ..................................................................................................................................................................
HLDTs ..................................................................................................................................................................
MDPVs .................................................................................................................................................................
0.50
0.65
0.90
1.00
Supplemental
2-day diurnal
plus hot soak
0.65
0.85
1.15
1.25
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1. Current Controls and Feasibility of
the Proposed Standards
Evaporative emissions from light-duty
vehicles and trucks will represent about
35 percent of the light-duty VOC
inventory and about 4 percent of the
benzene inventory in 2020. As
described earlier, we are proposing to
reduce the level of the evaporative
emission standards applicable to
diurnal and hot soak emissions from
these vehicles by about 20 to 50 percent.
These proposed standards are meant to
be effectively the same as the
evaporative emission standards in the
California LEV II program. Although the
California program contains evaporative
emissions standards that appear more
stringent than EPA Tier 2 standards if
one looks only at the level of the
standard, we believe they are essentially
equivalent because of differences in
testing requirements. For these same
reasons, some manufacturers likewise
view the programs as similar in
stringency. (See section VI.C.5 below for
further discussion of such test
differences, e.g., test temperatures and
fuel volatilities.) Thus, some
manufacturers have indicated that they
will produce 50-state evaporative
systems that meet both sets of standards
(manufacturers sent letters indicating
this to EPA in 2000).201 202 203 In
addition, a review of recent model year
certification results indicates that
essentially all manufacturers certify 50state systems, except for a few limited
cases where manufacturers have not yet
needed to certify a LEVII vehicle in
California due to the phase-in schedule.
Also, in recent discussions,
manufacturers have restated that they
plan to continue producing 50-state
evaporative systems in the future. Based
on this understanding, we do not project
additional VOC or air toxics reductions
from the evaporative standards we are
proposing today.204 Also, we do not
expect additional costs since we expect
that manufacturers will continue to
produce 50-state evaporative systems.
Therefore, harmonizing with
California’s LEV–II evaporative
emission standards would be an ‘‘antibacksliding’’ measure—that is, it would
prevent potential future backsliding as
manufacturers pursue cost
reductions.205 It would thus codify (i.e.,
lock in) the approach manufacturers
have already indicated they are taking
for 50-state evaporative systems.
We believe this proposed action
would be an important step to ensure
that the federal standards reflect the
lowest possible evaporative emissions,
and it also would provide states with
certainty that the emissions reductions
we project to occur due to 50-state
compliance strategies will in fact occur.
In addition, the proposed standards will
assure that manufacturers continue to
capture the abilities of available fuel
system materials to minimize
evaporative emissions.
We also considered the possibility of
whether it is feasible to achieve further
evaporative emission reductions from
motor vehicles. In this regard, it is
important to note that California’s LEV
II program includes partial zeroemission vehicle (ZEV) credits for
vehicles that achieve near zero
emissions (e.g., LDV evaporative
emission standards for both the 2-day
and 3-day diurnal plus hot soak tests are
0.35 grams/test, which are more
stringent than proposed standards).206
The credits would include full ZEV
credit for a stored hydrogen fuel cell
vehicle and 0.2 credits for (among other
categories for partial credit) a partial
zero emission vehicle (PZEV).207
Currently, only a fraction of California’s
certified vehicles (gasoline powered,
hybrid, and compressed natural gas
vehicles) meet California’s optional
PZEV standards, but this number is
expected to increase in coming
years.208 209 These limited PZEV
vehicles require additional evaporative
emissions technology or hardware (e.g.,
modifications to fuel tank and
secondary canister) than we expect to be
needed for vehicles meeting the
proposed standards. At this time, we
need to better understand the
evaporative system modifications (i.e.,
technology, costs, lead time, etc.)
potentially needed for other vehicles in
the fleet to meet PZEV-level standards
before we can rationally evaluate
whether to adopt more stringent
standards. For example, at this point we
cannot even determine whether the
PZEV technologies could be used
fleetwide or on only a limited set of
vehicles. Thus, in the near term, we lack
any of the information necessary to
determine if further reductions are
feasible, and if they could be achievable
considering cost, energy and safety
issues. However, we intend to consider
200 Larger vehicles may have greater non-fuel
evaporative emissions, probably due to an increased
amount of interior trim, vehicle body surface area,
and larger tires.
201 DaimlerChrysler, Letter from Reginald R.
Modlin to Margo Oge of U.S. EPA, May 30, 2000.
A copy of this letter can be found in Docket No.
EPA–HQ–OAR–2005–0036.
202 Ford, Letter from Kelly M. Brown to Margo
Oge of U.S. EPA, May 26, 2000. A copy of this letter
can be found in Docket No. EPA–HQ–OAR–2005–
0036.
203 General Motors, Letter from Samuel A.
Leonard to Margo Oge of U.S. EPA, May 30, 2000.
A copy of this letter can be found in Docket No.
EPA–HQ–OAR–2005–0036.
204 U.S. EPA, Office of Air and Radiation, Update
to the Accounting for the Tier 2 and Heavy-Duty
2005/2007 Requirements in MOBILE6, EPA420–R–
03–012, September 2003.
205 Anti-backsliding provisions can satisfy the
requirement in section 202 (l) (2) that emission
reductions of hazardous air pollutants be the
greatest achievable. Sierra Club v. EPA, 325 F. 3d
at 477.
206 California Air Resources Board, Fact Sheet,
LEV–II Amendments to California’s Low-Emission
Vehicle Regulations, February 1999
207 PZEV meets California super ultra low
emission vehicle exhaust emission standards and
have near zero evaporative emissions. California Air
Resources Board, News Release, ARB Modifies Zero
Emission Vehicle Regulation, April 24, 2003.
208 California Air Resources Board, Fact Sheet,
California Vehicle Emissions, April 8, 2004.
209 California Air Resources Board, Consumer
Information: 2006 California Certified Vehicles,
November 7, 2005.
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more stringent evaporative emission
standards in the future, and revisiting
this issue in a future rulemaking will
allow us time to obtain the important
necessary additional information for
such standards.
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2. Evaporative Standards Timing
We are proposing to implement
today’s evaporative emission standards
in model year 2009 for LDVs/LLDTs and
model year 2010 for HLDTs/MDPVs.
Today’s proposed rule is not expected to
be finalized until February 2007, at
which time many manufacturers already
will have begun or completed model
year 2008 certification. Thus, model
year 2009 is the earliest practical start
date of new standards for LDVs/LLDTs.
For HLDTs/MDPVs, the phase-in of the
existing Tier 2 evaporative emission
standards ends in model year 2009.
Thus, the model year 2010 is the earliest
start date possible for HLDTs/MDPVs.
Since the proposed standards are an
anti-backsliding measure and we believe
that manufacturers already meet these
standards, there is no need for
additional lead time beyond the
implementation dates proposed. We
request comment on this proposed
schedule.
3. Timing for Multi-Fueled Vehicles
As discussed earlier in this section,
manufacturers appear to view the Tier 2
and LEV II evaporative emission
programs as similar in stringency, and
thus, they have indicated that they will
produce 50-state evaporative systems
that meet both sets of standards. For
multi-fueled vehicles capable of
operating on alternative fuel (e.g., E85
vehicles—fuel is 85% ethanol and 15%
gasoline) and conventional fuel (e.g.,
gasoline),210 this commitment for 50state systems would still apply.
However, a few multi-fueled vehicles
were certified only on the conventional
fuel (gasoline) for the California LEV II
program even though they had 50-state
evaporative emission systems. For such
cases, manufacturers did not intend to
sell these vehicles for operation on the
alternative fuel (e.g. E85) in California
(only for operation on conventional fuel
in California), but they did certify and
plan to sell these vehicles in the federal
Tier 2 program for operation on the
alternative and conventional fuels.211
For these few types of multi-fueled
vehicles, manufacturers are potentially
at risk of not complying with the
210 40 CFR 86.1803–01 defines multi-fuel as
capable of operating on two or more different fuel
types, either separately or simultaneously.
211 For the Tier 2 program, multi-tier vehicles
must meet the same standards on conventional and
alternative fuel.
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proposed new evaporative emission
certification standards (which are
equivalent to California LEV II
certification standards) when operating
on the alternative fuel.
For such multi-fueled vehicles or
evaporative emission systems,
manufacturers would need a few
additional years of lead time to adjust
their evaporative systems to comply
with the proposed evaporative emission
certification standards when operating
on the alternative fuel. Thus, to reduce
the compliance risk for these types of
multi-fueled vehicles (or evaporative
families) when they first certify to the
more stringent evaporative standards,
the proposed evaporative emission
certification standards would apply to
the non-gasoline portion of multi-fueled
vehicles beginning in the fourth year of
the program—2012 for LDVs/LLDTs and
2013 for HLDTs/MDPVs. The proposed
evaporative emission certification
standards would be implemented in
2009 for LDVs/LLDTs and 2010 for
HLDTs/MDPVs for the gasoline portion
of multi-fueled vehicles and vehicles
that are not multi-fueled. We believe
this additional three years of lead time
would provide sufficient time for
manufacturers to make adjustments to
their new evaporative systems for multifueled vehicles, which are limited
product lines.
The provisions for in-use evaporative
emission standards described below in
section VI.C.4 would not change for
multi-fueled vehicles. We believe that
three additional years to prepare
vehicles (or evaporative families) to
meet the certification standards, and to
simultaneously make vehicle
adjustments from the federal in-use
experience of other vehicles (other
vehicles that are not multi-fueled) is
sufficient to resolve any issues for
multi-fueled vehicles. Therefore, the
proposed evaporative emission
standards would apply both for
certification and in-use beginning in
2012 for LDVs/LLDTs and 2013 for
HLDTs/MDPVs.
4. In-Use Evaporative Emission
Standards
As described earlier in this section,
we are proposing to adopt evaporative
emission standards that are equivalent
to California’s LEV II standards for all
light duty vehicles, light trucks, and
medium duty passenger vehicles.
Currently, the Tier 2 evaporative
emission standards are the same for
certification and in-use vehicles.
However, the California LEV II program
permits manufacturers to meet less
stringent standards in-use for a short
time period in order to account for
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potential variability in-use during the
initial years of the program when
technical issues are most likely to
arise.212 The LEV II program specifies
that in-use evaporative emission
standards of 1.75 times the certification
standards will apply for the first three
model years after an evaporative family
is first certified to the LEV II standards
(only for vehicles introduced prior to
model year 2007, the year after 100
percent phase-in).213 214 An interim
three-year period was considered
sufficient to accommodate any technical
issues that may arise.
Federal in-use conditions may raise
unique issues (e.g., salt/ice exposure) for
evaporative systems certified to the new
proposed standards (which are
equivalent to the LEV II standards), and
thus, we propose to adopt a similar,
interim in-use compliance provision for
federal vehicles. As with the LEV II
program, this provision would enable
manufacturers to make adjustments for
unforeseen problems that may occur inuse during the first three years of a new
evaporative family. Like California, we
believe that a three-year period is
enough time to resolve these problems,
because it allows manufacturers to gain
real world experience and make
adjustments to a vehicle within a typical
product cycle.
Depending on the vehicle weight class
and type of test, the Tier 2 certification
standards are 1.3 to 1.9 times the LEV
II certification standards. On average the
Tier 2 standards are 1.51 times the LEV
II certification standards. Thus, to
maintain the same level of stringency
for the in-use evaporative emission
standards provided by the Tier 2
program, we propose to apply the Tier
2 standards in-use for only the first
three model years after an evaporative
family is first certified under today’s
proposed standards instead of the 1.75
multiplier implemented in the
California LEV II program. Since the
proposed evaporative emission
certification standards (equivalent to
LEV II standards) would be
implemented in model year 2009 for
LDVs/LLDTs and model year 2010 for
HLDTs/MDPVs, these same certification
212 California Air Resources Board, ‘‘LEV II’’ and
‘‘CAP 2000’’ Amendments to the California Exhaust
and Evaporative Emission Standards and Test
Procedures for Passenger Cars, Light-Duty Trucks
and Medium-Duty Vehicles, and to the Evaporative
Emission Requirements for Heavy-Duty Vehicles,
Final Statement of Reasons, September 1999.
213 1.75 times the 3-day diurnal plus hot soak and
2-day diurnal plus hot soak standards.
214 For example, evaporative families first
certified to LEV II standards in the 2005 model year
shall meet in-use standards of 1.75 times the
evaporative certification standards for 2005, 2006,
and 2007 model year vehicles.
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standards would apply in-use beginning
in model year 2012 for LDVs/LLDTs and
model year 2013 for HLDTs/MDPVs.215
5. Existing Differences Between
California and Federal Evaporative
Emission Test Procedures
As described above, the California
LEV II evaporative emission standards
are numerically more stringent than
EPA’s Tier 2 standards, but due to
differences in California and EPA
evaporative test requirements, EPA and
most manufacturers view the programs
as similar in stringency. The Tier 2
evaporative program requires
manufacturers to certify the durability
of their evaporative emission systems
using a fuel containing the maximum
allowable concentration of alcohols
(highest alcohol level allowed by EPA in
the fuel on which the vehicle is
intended to operate, i.e., a ‘‘worst case’’
test fuel). Under current requirements,
this fuel would be about 10 percent
ethanol by volume.216 (We are retaining
these Tier 2 durability requirements for
the proposed evaporative emissions
program.) California does not require
this provision. To compensate for the
increased vulnerability of system
components to alcohol fuel,
manufacturers have indicated that they
will produce a more durable evaporative
emission system than the Tier 2
numerical standards would imply, using
the same low permeability hoses and
low loss connections and seals planned
for California LEV II vehicles.
As shown in Table VI.C–2, combined
with the maximum alcohol fuel content
for durability testing, the other key
differences between the federal and
California test requirements are fuel
volatilities, diurnal temperature cycles,
and running loss test temperatures.217
The EPA fuel volatility requirement is 2
psi greater than that of California. The
high end of EPA’s diurnal temperature
range, is 9° F lower than that of
California. Also, EPA’s running loss
temperature is 10° F lower than
California’s.
TABLE VI.C–2.—DIFFERENCES IN TIER 2 AND LEV II EVAPORATIVE EMISSION TEST REQUIREMENTS
Test requirement
EPA tier 2
Fuel volatility (Reid Vapor Pressure in psi) .......................................................................................................
Diurnal temperature cycle (degrees F) ..............................................................................................................
Running loss test temperature (degrees F) ......................................................................................................
9 .......................
72 to 96 ............
95 .....................
California LEV II
7.
65 to 105.
105.
In addition to the cold temperature
NMHC and evaporative emission
standards we are proposing, we
evaluated an additional option for
reducing hydrocarbons from light-duty
vehicles. This option would further
align the federal light-duty exhaust
emissions control program with that of
California. We are not proposing this
option today for the reasons described
below. It is possible that a future
evaluation could result in EPA
reconsidering the option of harmonizing
the Tier 2 program with California’s
LEV–II program or otherwise seeking
emission reductions beyond those of the
Tier 2 program and those being
proposed today.219
As explained earlier, section 202(l)(2)
requires EPA to adopt regulations that
contain standards which reflect the
greatest degree of emissions reductions
achievable through the application of
technology that will be available, taking
into consideration existing motor
vehicle standards, the availability and
costs of the technology, and noise,
energy and safety factors. The cold
temperature NMHC program proposed
today is appropriate under section
202(l)(2) as a near-term control: That is,
a control that can be implemented
relatively soon and without disruption
to other existing vehicle emissions
control program. We are not proposing
long-term (i.e., controls that require
longer lead time to implement) at this
time because we lack the information
necessary to assess appropriate longterm controls. We believe it will be
important to address the
appropriateness of further MSAT
controls in the context of compliance
with other significant vehicle emissions
regulations (discussed below).
In the late 1990’s both the EPA and
the California Air Resources Board
finalized new and technologically
challenging light-duty vehicle/truck
emission control programs. The EPA
program, known as Tier 2, focused on
reducing NOX emissions from the lightduty fleet. The California program,
which is the second generation of their
low emission vehicle (LEV) program
and is known as LEV–II, focuses
primarily on reducing hydrocarbons by
tightening the light-duty NMOG
standards. Both programs are expected
to present the manufacturers with
significant challenges, and will require
the use of hardware and emission
control strategies not used in the fleet
under previously existing programs.
Both programs will achieve significant
reductions in emissions. Taken as a
whole, the Tier 2 program presents the
manufacturers with significant
challenges in the coming years. Bringing
essentially all passenger vehicles under
the same emission control program
regardless of their size, weight, and
application is a major engineering
challenge. The Tier 2 program
represents a comprehensive, integrated
package of exhaust, evaporative, and
fuel quality standards which will
achieve significant reductions in
215 For example, evaporative families first
certified to the proposed LDV/LLDT evaporative
emission standards in the 2011 model year would
be required to meet the Tier 2 LDV/LLDT
evaporative emission standards in-use for 2011,
2012, and 2013 model year vehicles (applying Tier
2 standards in-use would be limited to the first
three years after introduction of a vehicle), and
2014 and later model year vehicles of such
evaporative families would be required to meet the
proposed LDV/LLDT evaporative emission
standards in-use.
216 Manufacturers are required to develop
deterioration factors using a fuel that contains the
highest legal quantity of ethanol available in the
U.S.
217 Running loss emissions means evaporative
emissions as a result of sustained vehicle operation
(average trip in an urban area) on a hot day. The
running loss test requirement is part of the 3-day
diurnal plus hot soak test sequence.
218 EPA may require comparative data from both
federal and California tests.
219 See Sierra Club v. EPA, 325 F.3d at 480 (EPA
can reasonably determine that no further reductions
in MSATs are presently achievable due to
uncertainties created by other recently promulgated
regulatory provisions applicable to the same
vehicles).
Currently, California accepts
evaporative emission results generated
on the federal test procedure (using
federal test fuel), because available data
indicates the federal procedure to be a
‘‘worst case’’ procedure. In addition,
manufacturers can obtain federal
evaporative certification based upon
California results (meeting LEV II
standards under California fuels and test
conditions), if they obtain advance
approval from EPA.218
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D. Opportunities for Additional Exhaust
Control Under Normal Conditions
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NMHC, NOX, and PM emissions from all
light-duty vehicles in the program.
These reductions will include
significant reductions in MSATs.
Emission control in the Tier 2 program
will be based on the widespread
implementation of advanced catalyst
and related control system technology.
The standards are very stringent and
will require manufacturers to make full
use of nearly all available emission
control technologies.
Today the Tier 2 program remains
early in its phase-in. Cars and lighter
trucks will be fully phased into the
program with the 2007 model year, and
the heavier trucks won’t be fully entered
into the program until the 2009 model
year. Even though the lighter vehicles
will be fully phased in by 2007, we
expect the characteristics of this
segment of the fleet to remain in a state
of transition at least through 2009,
because manufacturers will be making
adjustments to their fleets as the larger
trucks phase in. The Tier 2 program is
designed to enable vehicles certified to
the LEV–II program to cross over to the
federal Tier 2 program. At this point in
time, however, it is difficult to predict
the degree to which this will occur. The
fleetwide NMOG levels of the Tier 2
program will ultimately be affected by
the manner in which LEV–II vehicles
are certified within the Tier 2 bin
structure, and vice versa. We intend to
carefully assess these two programs as
they evolve and periodically evaluate
the relative emission reductions and the
integration of the two programs.
Today’s proposal addresses toxics
emissions from vehicles operating at
cold temperatures. The technology to
achieve this is already available and we
project that compliance will not be
costly. However, we do not believe that
we could reasonably propose further
controls at this time. There is enough
uncertainty regarding the interaction of
the Tier 2 and LEV–II programs to make
it difficult to evaluate today what might
be achievable in the future. Depending
on the assumptions one makes, the
LEV–II and Tier 2 programs may or may
not achieve very similar NMOG
emission levels. Therefore, the eventual
Tier 2 baseline technologies and
emissions upon which new standards
would necessarily be based are not
known today. Additionally, we believe
it is important for manufacturers to
focus in the near term on developing
and implementing robust technological
responses to the Tier 2 program without
the distraction or disruption that could
result from changing the program in the
midst of its phase-in. We believe that it
may be feasible in the longer term to
seek additional emission reductions
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from the base Tier 2 program, and the
next several years will allow an
evaluation based on facts rather than
assumptions. For these reasons, we are
deferring a decision on seeking
additional NMOG reductions from the
base Tier 2 program.
E. Vehicle Provisions for Small Volume
Manufacturers
Prior to issuing a proposal for this
proposed rulemaking, we analyzed the
potential impacts of these regulations on
small entities. As a part of this analysis,
we convened a Small Business
Advocacy Review Panel (SBAR Panel,
or the Panel). During the Panel process,
we gathered information and
recommendations from Small Entity
Representatives (SERs) on how to
reduce the impact of the rule on small
entities, and those comments are
detailed in the Final Panel Report which
is located in the public record for this
rulemaking (Docket EPA–HQ–OAR–
2005–0036). Based upon these
comments, we propose to include lead
time transition and hardship provisions
that would be applicable to small
volume manufacturers as described
below in section VI.E.1 and VI.E.2. For
further discussion of the Panel process,
see section XII.C of this proposed rule
and/or the Final Panel Report.
As discussed in more detail in section
XII.C in addition to the major vehicle
manufacturers, three distinct categories
of businesses relating to highway lightduty vehicles would be covered by the
new vehicle standards: Small volume
manufacturers (SVMs), independent
commercial importers (ICIs),220 and
alternative fuel vehicle converters.221
We define small volume manufacturers
as those with total U.S. sales less than
15,000 vehicles per year, and this status
allows vehicle models to be certified
under a slightly simpler certification
process. For certification purposes,
SVMs include ICIs and alternative fuel
vehicle converters since they sell less
than 15,000 vehicles per year.
About 34 out of 50 entities that certify
vehicles are SVMs, and the Panel
identified 21 of these 34 SVMs that are
small businesses as defined by the
Small Business Administration criteria
(5 manufacturers, 10 ICIs, and 6
converters). Since a majority of the
SVMs are small businesses and all
220 ICIs are companies that hold a Certificate (or
certificates) of Conformity permitting them to
import nonconforming vehicles and to modify these
vehicles to meet U.S. emission standards.
221 Alternative fuel vehicle converters are
businesses that convert gasoline or diesel vehicles
to operate on alternative fuel (e.g., compressed
natural gas), and converters must seek a certificate
for all of their vehicle models.
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SVMs have similar characteristics as
described below in section VI.E.1, the
Panel recommended that we apply the
lead time transition and hardship
provisions to all SVMs. These
manufacturers represent just a fraction
of one percent of the light-duty vehicle
and light-duty truck sales. Our proposal
today is consistent with the Panel’s
recommendation.
1. Lead Time Transition Provisions
In these types of vehicle businesses,
predicting sales is difficult and it is
often necessary to rely on other entities
for technology (see earlier discussions
in section VI on technology needed to
meet the proposed standards).222 223
Moreover, percentage phase-in
requirements pose a dilemma for an
entity such as a SVM that has a limited
product line. For example, it is
challenging for a SVM to address
percentage phase-in requirements if the
manufacturer makes vehicles in only
one or two test groups. Because of its
very limited product lines, a SVM could
be required to certify all their vehicles
to the new standards in the first year of
the phase-in period, whereas a full-line
manufacturer (or major manufacturer)
could utilize all four years of the phasein. Thus, similar to the flexibility
provisions implemented in the Tier 2
rule, the Panel recommended that we
allow SVMs, manufacturers with sales
less than 15,000 vehicles per year
(includes all vehicle small entities that
would be affected by this rule, which
are the majority of SVMs) the following
flexibility options for meeting cold
temperature NMHC standards and
evaporative emission standards as an
element of determining appropriate lead
time for these entities to comply with
the standards.
For cold NMHC standards, the Panel
recommended that SVMs simply
comply with the standards with 100
percent of their vehicles during the last
year of the 4 year phase-in period. Since
these entities could need additional lead
time flexibility and proposed standards
for light-duty vehicles and light lightduty trucks would begin in model year
2010 and would end in model year 2013
(25%, 50%, 75%, 100% phase-in over 4
222 For example, as described later in section
VI.E.3, ICIs may not be able to predict their sales
because they are dependent upon vehicles brought
to them by individuals attempting to import
uncertified vehicles.
223 SMVs (those with sales less than 15,000
vehicles per year) include ICIs, alternative fuel
vehicle converters, companies that produce
specialty vehicles by modifying vehicles produced
by others, and companies that produce small
quantities of their own vehicles, but rely on major
manufacturers for engines and other vital emission
related components.
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years), we propose that the SVM
provision would be 100 percent in
model year 2013. Also, since the
proposed standard for heavy light-duty
trucks and medium-duty passenger
vehicles would start in 2012 (25%, 50%,
75%, 100% phase-in over 4 years), we
propose that the SVM provision would
be 100 percent in model year 2015.
In regard to evaporative emission
standards, the Panel recommended that
since the proposed evaporative
emissions standards would not have
phase-in years, we allow SVMs to
simply comply with standards during
the third year of the program (we have
implemented similar provisions in past
rulemakings). Given the additional
challenges that SVMs face, as noted
above, we believe that this
recommendation is reasonable.
Therefore, for a 2009 model year start
date for light-duty vehicles and light
light-duty trucks, we propose that SVMs
meet the evaporative emission standards
in model year 2011. For a model year
2010 implementation date for heavy
light-duty trucks and medium-duty
passenger vehicles, we propose that
SVMs comply in model year 2012.
2. Hardship Provisions
In addition, the Panel recommended
that hardship provisions be extended to
SVMs for the cold temperature NMHC
and evaporative emission standards as
an aspect of determining the greatest
emission reductions feasible. These
entities could, on a case-by-case basis,
face hardship more than major
manufacturers (manufacturers with
sales of 15,000 vehicles or more per
year), and we are proposing this
provision to provide what could prove
to be a needed safety valve for these
entities. SVMs would be allowed to
apply for up to an additional 2 years to
meet the 100 percent phase-in
requirements for cold NMHC and the
delayed requirement for evaporative
emissions. As with hardship provisions
for the Tier 2 rule, we propose that
appeals for such hardship relief must be
made in writing, must be submitted
before the earliest date of
noncompliance, must include evidence
that the noncompliance will occur
despite the manufacturer’s best efforts to
comply, and must include evidence that
severe economic hardship will be faced
by the company if the relief is not
granted.
We would work with the applicant to
ensure that all other remedies available
under this rule are exhausted before
granting additional relief. To avoid the
very existence of the hardship provision
prompting SVMs to delay development,
acquisition and application of new
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technology, we want to make clear that
we would expect this provision to be
rarely used. Our proposed rule contains
numerous flexibilities for all
manufacturers and it delays
implementation dates for SVMs, which
effectively provides them more time. We
would expect small volume
manufacturers to prepare for the
applicable implementation dates in
today’s proposed rule.
3. Special Provisions for Independent
Commercial Importers (ICIs)
Although the SBAR panel did not
specifically recommend it, we are
proposing to allow ICIs to participate in
the averaging, banking, and trading
program for cold temperature NMHC
fleet average standards (as described in
Table IV.B.–1), but with appropriate
constraints to ensure that fleet averages
will be met. The existing regulations for
ICIs specifically bar ICIs from
participating in emission related
averaging, banking, and trading
programs unless specific exceptions are
provided (see 40 CFR 85.1515(d)). The
concern is that they may not be able to
predict their sales and control their fleet
average emissions because they are
dependent upon vehicles brought to
them by individuals attempting to
import uncertified vehicles. However,
an exception for ICIs to participate in an
averaging, banking, and trading program
was made for the Tier 2 NOX fleet
average standards, and today we
propose to apply a similar exception for
the cold temperature NMHC fleet
average standards.
If an ICI is able to purchase credits or
to certify a test group to a family
emission level (FEL) below the
applicable cold temperature NMHC fleet
average standard, we would permit the
ICI to bank credits for future use. Where
an ICI desires to certify a test group to
a FEL above the applicable fleet average
standard, we would permit them to do
so if they have adequate and appropriate
credits. Where an ICI desires to certify
to an FEL above the fleet average
standard and does not have adequate or
appropriate credits to offset the
vehicles, we would permit the
manufacturer to obtain a certificate for
vehicles using such a FEL, but would
condition the certificate such that the
manufacturer can only produce vehicles
if it first obtains credits from other
manufacturers or from other vehicles
certified to a FEL lower than the fleet
average standard during that model
year.
Our experience over the years through
certification indicates that the nature of
the ICI business is such that these
companies cannot predict or estimate
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their sales of various vehicles well.
Therefore, we do not have confidence in
their ability to certify compliance under
a program that would allow them
leeway to produce some vehicles to a
higher FEL now but sell vehicles with
lower FELs later, such that they were
able to comply with the fleet average
standard. We also cannot reasonably
assume that an ICI that certifies and
produces vehicles one year, would
certify or even be in business the next.
Consequently, we propose that ICIs not
be allowed to utilize the deficit
carryforward provisions of the proposed
ABT program.
VII. Proposed Gasoline Benzene
Control Program
A. Overview of Today’s Proposed Fuel
Control Program
As discussed in sections I, IV, and V
above, people experience elevated risk
of cancer and other health effects as a
result of inhalation of air toxics. Mobile
sources are responsible for a significant
portion of this risk. As required by
section 202(l) of the Clean Air Act, EPA
has evaluated options to reduce MSAT
emissions by setting standards for motor
vehicle fuel. We have determined that
there are fuel-related technologies
available to feasibly reduce MSAT
emissions and that these reductions are
achievable, considering cost, energy,
and other factors. These feasible
reductions would be in addition to
those resulting from actions taken by the
industry in response to the earlier fuelrelated MSAT programs described in
section V above. Accordingly, we
believe a fuel control program is
necessary and appropriate to reduce air
toxics emissions from motor vehicles to
the greatest extent achievable (in
addition to the programs proposed
elsewhere in this notice to reduce
MSAT emissions by changes to
gasoline-powered motor vehicles and
gas cans). This section of the preamble
describes our proposed fuel control
program.
The section begins with a detailed
description of today’s proposed
program. In summary, we propose that
beginning January 1, 2011, refiners
would meet an average gasoline benzene
content standard of 0.62% by volume on
all their gasoline (reformulated and
conventional) nationwide.224 We also
propose that refiners could generate
benzene credits and use or sell them as
a part of a nationwide averaging,
banking, and trading (ABT) program.
224 The State of California has a similar benzene
standard and gasoline sold there is not covered by
this proposal. For more information, see California
Code of Regulations, Title 13 Section 2262.
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We believe that the proposed benzene
standard, combined with the proposed
ABT program, would result in the
largest feasible overall reductions in
benzene emissions of any potential fuelbased MSAT control program. Finally,
as an aspect of achieving the greatest
emission reductions, we also propose
special compliance flexibility for
approved small refiners.
This section then describes in detail
how we arrived at the proposed
program. We discuss a range of potential
approaches to reducing MSATs through
changes in fuel, concluding that
benzene emissions would be
significantly more responsive to fuel
changes than emissions of any other
fuel-related MSAT. This is followed by
discussion of alternate methods of
reducing benzene emissions, resulting
in the proposed approach of directly
controlling benzene content. We also
discuss how we arrived at the proposed
level of 0.62 volume percent (vol%) for
the benzene standard. We discuss why
we believe that incorporating the
proposed ABT program would be
crucial for the effectiveness of the
overall benzene control program and
describe how the system would work.
Finally, we review the
recommendations of the special panel
that was convened to assess the
potential for disproportionate impacts of
the proposed program on small refiners,
and present our reasoning for the
special small refiner provisions we are
proposing today.
Today’s proposed action would fulfill
several statutory and regulatory goals for
gasoline-related MSAT emissions,
which are discussed in more detail in
this section. The program would meet
our commitment in the MSAT1 program
to consider further MSAT control. The
program would also allow EPA to
streamline the regulatory provisions for
the air toxics performance requirements
of the reformulated gasoline (RFG) and
Anti-dumping programs. The expected
levels of benzene control by individual
refiners under this proposal, combined
with other gasoline controls such as
sulfur, RVP, and VOC controls, mean
that compliance with these provisions is
expected to lead to compliance with the
annual average requirements for
benzene and toxics performance for RFG
and the annual average Anti-dumping
toxics performance for conventional
gasoline. EPA is therefore proposing
that upon full implementation in 2011,
the regulatory provisions for the
benzene control program would become
the single regulatory mechanism used to
implement these RFG and Antidumping annual average toxics
requirements, replacing the current RFG
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and Anti-dumping annual average
provisions (although the 1.3 vol%
benzene cap would still apply for RFG).
The proposed benzene control program
would also replace the MSAT1
requirements. In addition, the program
would satisfy certain fuel MSAT
conditions of the Energy Policy Act of
2005. By consciously designing this
proposed program to address these
separate but related goals, we would
significantly consolidate and simplify
the existing national fuel-related MSAT
regulatory program.
Finally, this section concludes with a
detailed summary of our assessment of
the technological feasibility for different
types of refineries, and the refining
industry as a whole, to meet the
program as proposed. We request
general and specific comment on all
aspects of the proposed program, and
we request that comments include
supporting data whenever possible.
B. Description of the Proposed Fuel
Control Program
Today’s proposed program has three
main components, the development of
each of which is further described later
in this section:
—A gasoline benzene content standard.
We propose that an annual average
gasoline benzene standard of 0.62
vol% be implemented beginning
January 1, 2011. This single standard
would apply to all gasoline, both
reformulated (RFG) and conventional
(CG) nationwide (except for gasoline
sold in California, which is already
covered by a similar state program).
—An averaging, banking, and trading
(ABT) program. From 2007–2010
refiners could generate benzene
credits by taking early steps to reduce
gasoline benzene levels. Beginning in
2011 and continuing indefinitely,
refiners could generate credits by
producing gasoline with benzene
levels below the 0.62% average
standard. Refiners could apply the
credits towards company compliance,
‘‘bank’’ the credits for later use, or
transfer (‘‘trade’’) them to other
refiners nationwide (outside of
California) under the proposed
program. Under this program, refiners
could use credits to achieve
compliance with the benzene content
standard, regardless of their actual
gasoline benzene levels.225
—Hardship provisions. Refiners
approved as ‘‘small refiners’’ would
have access to special temporary relief
provisions. In addition, any refiner
225 However, the per-gallon benzene cap (1.3
vol%) in the RFG program would continue to apply
separately.
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facing extreme unforeseen
circumstances or extreme hardship
circumstances could apply for similar
temporary relief.
C. Development of the Proposed
Gasoline Benzene Standard
EPA believes that benzene control is
by far the most effective fuel-based
means of achieving MSAT emissions
control, as described in this section.
There are other options that can target
individual MSATs or reduce overall
VOCs and thereby reduce MSATs as
well. We have evaluated these other
options, as discussed below, and our
analysis indicates that the potential
MSAT reductions would be
considerably smaller and more
expensive.
1. Why Are We Focusing on Controlling
Benzene Emissions?
We considered controlling emissions
of several MSATs through changes to
fuel parameters. There are only a
limited number of MSATs that are
affected through fuel changes, each of
which we discuss below. For several
reasons, we have concluded that the
most effective and appropriate means of
reducing fuel-related MSATs is to
reduce the benzene emissions
attributable to gasoline.
Benzene emissions can be reduced
much more significantly through fuel
changes than can emissions of other
MSATs. Relatively small changes in
gasoline can result in very significant
reductions in benzene emissions. This
relative responsiveness of benzene
emissions to fuel controls (specifically
to control of gasoline benzene content,
as discussed in the next section) is
coupled with little negative impact on
other important characteristics of
gasoline or refining processes. A related
and critical advantage of fuel control of
benzene emissions, as compared to fuel
control of emissions of other MSATs as
discussed below, is that controlling
benzene emissions does not
significantly increase emissions of other
MSATs.226
In determining an appropriate
approach to fuel-related MSAT control,
a key consideration was octane value.
226 A key tool in evaluating the potential for fuel
changes to affect MSAT emissions is EPA’s
Complex Model. This model relates changes in
gasoline parameters with emissions of specific
MSATs and was developed for refiners and EPA to
assess compliance with the RFG, Anti-dumping,
and MSAT1 programs. (See section V.D.1 above.)
Given a set of gasoline parameters, it estimates the
emissions of an average vehicle based on a large set
of fuel effects data. We further discuss the Complex
Model, as well as other sources of information the
relationships between fuel changes and MSAT
emissions, in chapter 6 of the RIA.
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Among potential approaches to fuelrelated MSAT emission reduction, only
benzene emission reduction can avoid
major losses in octane value and the
negative cost and environmental
consequences discussed below of
replacing that lost octane value.
Finished gasoline must meet minimum
specifications for octane value; these
specifications are tied to the operational
needs of motor vehicles. Thus, refiners
must be keenly aware of how any
changes in gasoline production might
reduce the octane value of their fuel,
what approaches to restore the octane
value might be available, and the costs
in material and operational changes of
any selected approach.
There are a limited number of
approaches refiners have at their
disposal to restore gasoline octane value
lost through control of MSAT emissions.
These approaches vary in their
economics and effectiveness, and their
availability may be limited by the
specific configuration of a given
refinery. However, all methods of
replacing octane value have cost
implications, and as shown in the next
paragraph, air toxics implications as
well.
In the case of changes in gasoline
production that are intended to reduce
MSAT emissions, it is also important to
consider whether restoring any lost
octane might itself significantly increase
other MSAT emissions. Some methods
of replacing octane value can increase
other MSATs. For example, increasing
aromatics would increase benzene
emissions; adding MTBE would
increase formaldehyde emissions; and
adding ethanol would increase
acetaldehyde emissions. Given the very
large MSAT emission reduction
associated with benzene control, these
impacts on other MSATs are relatively
insignificant. However, in the case of
changes in other fuel qualities (e.g.,
aromatics control), the relative impacts
on other MSATs would be greater.
We encourage comment on our
decision to propose a program that
directly controls gasoline benzene
content, including comments on each of
the alternate approaches to MSAT
control discussed in the following
paragraphs.
a. Other MSAT Emissions
As alternatives to the proposed
program focusing on benzene emission
reductions, we considered other MSATs
that are responsive to fuel-based
emission control. Each of these is
discussed next.
Polycyclic Organic Matter, or POM, is
composed of a number of combustion
products of gasoline. According to the
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Complex Model, POM emissions are a
function of exhaust VOC. Several fuel
parameters including volatility and
sulfur content affect VOC emissions. As
discussed below, little data exists about
the potential impacts of changes in
gasoline volatility and sulfur content on
VOC, and thus POM, emissions from
new Tier 2-compliant vehicles. In any
event, because POM is only a tiny
fraction of vehicle VOC emissions, we
expect that further changes in these fuel
parameters would have only small
effects on POM. As a result, we are not
proposing fuel controls to address POM
emissions in today’s action.
Emissions of the compound 1,3butadiene can be reduced by reducing
the olefin content of gasoline. However,
olefin reduction yields relatively small
reductions in 1,3-butadiene and can
increase VOC emissions. In addition,
olefin reduction significantly affects
octane, with the negative cost and
MSAT emissions consequences of
octane replacement. We are thus not
proposing to address 1,3-butadiene
emissions through fuel changes.
Emissions of the compound
formaldehyde can only be effectively
reduced by reducing use of the octane
enhancer methyl tertiary butyl ether
(MTBE). This is because formaldehyde
increases significantly as a combustion
product when MTBE is added to
gasoline. Formaldehyde also increases
to a lesser extent when ethanol is added
to gasoline, as described below. For a
number of years, MTBE has been used
as a cost-effective way to meet
mandated fuel oxygenate requirements
and to boost octane. In recent years,
many states have banned the use of
MTBE because it has leaked from
storage tanks and caused significant
groundwater contamination. More
recently, in the wake of the removal of
the oxygenate requirement in the Energy
Policy Act of 2005, many refiners are
taking action to remove MTBE from
their gasoline as soon as possible. As a
result, MTBE use and the resulting
formaldehyde emissions are expected to
continue to decline, and no additional
federal action appears warranted at this
time.
The compound acetaldehyde is a
combustion product of gasoline when
ethanol is added. Controlling
acetaldehyde would require reductions
in the use of ethanol as a gasoline
additive. However, the Energy Policy
Act of 2005 (section 1501) includes a
renewable fuels program that will
increase use of ethanol in gasoline
nationwide. That Act requires a study of
the Act’s impacts on public health, air
quality, and water resources. We
accordingly intend to defer further
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evaluation of acetaldehyde emissions to
the analyses associated with the Energy
Policy Act.
b. MSAT Emission Reductions Through
Lowering Gasoline Volatility or Sulfur
Content
We also considered two approaches to
fuel-related MSAT control that would
involve increasing the stringency of two
existing emission control programs.
Both were originally promulgated
primarily to address ozone but also have
the effect of reducing some MSAT
emissions by virtue of their control of
VOC emissions. As explained in section
V, the Tier 2 program included the
pairing of lower vehicle emissions
standards with large reductions in
gasoline sulfur levels. The low sulfur
fuel helped enable development of more
advanced catalytic aftertreatment
systems needed to meet the stringent
tailpipe standards. These actions will
result in large reductions of VOC, NOX,
and air toxics emissions. In
development of today’s proposal, we
considered whether further reductions
in fuel sulfur would bring significant
additional reductions in MSAT
emissions.
The second program considered for
additional stringency was the gasoline
volatility program, which was
implemented in 1989 to address
evaporative VOC emissions from
gasoline vehicles. Reducing the
volatility of gasoline can reduce
evaporative VOC emissions as well as
exhaust emissions. Evaporative VOC
emissions include benzene. As a result,
in developing this proposal we have
considered whether further reductions
in gasoline volatility may be effective in
further reducing MSAT emissions.
In the cases of both further reductions
in RVP and sulfur reductions below the
current 30 ppm standard, the available
data is not sufficient to conclude that
additional control of either would be a
valuable MSAT emission reduction
strategy. Historic data suggest that
reducing both RVP and sulfur content
would reduce overall VOC emissions
from vehicles, in turn reducing both
MSATs and ozone formation. However,
vehicles complying with the stringent
new Tier 2 emission standards have
dramatically lower VOC emissions than
earlier vehicles. Furthermore, it is likely
that VOC emissions for these vehicles
would react differently to RVP and
sulfur control than older vehicles, as
new catalysts and control systems may
have more or less sensitivity to these
variables. Since the dominant effect on
MSAT emissions of changing these fuel
parameters is through their impact on
total VOC mass, it is not possible to
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i. Gasoline Sulfur Content
In general, reducing gasoline sulfur
levels increases the effectiveness of the
catalytic converter at destroying
unburned fuel and other VOCs in
vehicle exhaust. Catalytic converters
contain a variety of physical and
chemical structures that act as reaction
sites for conversion of raw exhaust gases
into less harmful ones before they are
emitted into the atmosphere. Over time,
sulfur compounds in the exhaust gases
interfere with these processes, making
the catalyst less effective under normal
driving conditions.227 Since many air
toxics are part of the exhaust VOCs,
reduction of fuel sulfur would be
expected to reduce air toxics emissions.
As with the Tier 2 program, however,
desulfurizing gasoline further would
reduce gasoline octane. Most options for
recovering this lost octane (e.g.,
increasing aromatics) would result in
some offsetting MSAT emissions
increases.
EPA primarily uses two computer
models for examining emissions
impacts when considering changes in
fuel properties: the Complex Model and
the MOBILE model. The Complex
Model (CM) was developed as a
compliance tool that refiners use to
ensure their gasoline meets its baseline
requirements under the RFG, Antidumping, and MSAT1 programs. Given
a set of fuel parameters, it estimates the
emissions of an average vehicle using
regression relationships drawn from a
large set of fuel effects data. The CM
contains data on test fuels with sulfur
levels as low as 5 ppm, but is based on
the Auto/Oil research programs of the
early 1990s, and reflects performance of
vehicles on the road during that time
period. With a sulfur reduction from 30
ppm to 10 ppm applied to average 2003
conventional gasoline, the CM projects
a decrease of approximately 1% for
exhaust benzene, NOX and CO.
MOBILE was developed to estimate
aggregate emissions on a county, state,
or national scale. It uses a fuel effects
dataset that includes the CM dataset
with some updates, along with driving
data, to predict emissions inventories of
pollutants for a specified time period
and area of the country. MOBILE6.2
contains updates from a small number
of LEV and ULEV vehicles in addition
to the CM dataset, but applies a lower
limit of 30 ppm to fuel sulfur content
being modeled to avoid extrapolation
beyond the range of available emissions
data.
Based primarily on the above models,
the analyses done for the Tier 2
rulemaking suggested benzene emission
reductions on the order of 9% could be
expected in 2020 as a result of the fuel
sulfur reduction expected from that
program alone (the final Tier 2 program
included low sulfur gasoline as well as
tightened vehicle standards).228 A
recent study done on vehicles meeting
LEV, TLEV, and ULEV standards
indicates that sulfur reductions from 30
to 5 ppm may reduce NMHC by more
than 10%, bringing similar reductions
in air toxics.229 Additional analyses
done by EPA on sulfur reductions in
this range suggest VOC emission
reductions on the order of 5% may be
expected, with refining costs estimated
at about a half cent per gallon. Given
these analyses using available data,
using sulfur reductions as air toxics
control alone would not be as costeffective as other options in this
proposal. Further discussion of the
feasibility and costs are available in
Chapters 6 and 9, respectively, of the
RIA.
Since our models do not reflect the
significant improvements in emissions
control technology over the past decade,
more fuel effects studies are necessary
on newest-technology vehicles before
going forward with sulfur control. A
small cooperative test program is
currently underway between EPA and
the Alliance of Automobile
Manufacturers to evaluate the effects of
reducing sulfur below 10 ppm on Tier
2 Bin 5 compliant vehicles.
In addition to potential air toxics
reductions from adjustment of gasoline
sulfur to 10 ppm, reducing sulfur may
also provide significant VOC and NOX
emission reductions. These emission
reductions may be important for states
in complying with the National
227 For further discussion on sulfur effects on
emissions, see the Tier 2 Regulatory Impact
Analysis, EPA 420–R–99–023.
228 Tier 2 Regulatory Impact Analysis, EPA 420–
R–99–023
229 AAM-Honda fuel effects study, 2000
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properly assess the impact of changes in
these fuel parameters on MSAT
emissions without additional data. We
have begun collecting data on some of
these new vehicles, but more work will
be required before we can draw
conclusions about the effectiveness of
these fuel controls in reducing MSAT
emissions. Therefore, we are not
proposing additional control of gasoline
volatility or sulfur at this time, but will
continue to evaluate them for possible
future action. We request comments on
these potential fuel controls as emission
reduction strategies, in particular for
MSAT emissions, including any data
that does or does not support the
effectiveness of such controls.
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Ambient Air Quality Standards
(NAAQS) for ozone. Since the
implementation of the RFG program,
several states and localities have made
their own unique fuel property
requirements in an effort to further
improve air quality.230 As a result, by
summer 2004 the gasoline distribution
and marketing system in the U.S. had to
differentiate between more than 12
different fuel specifications, when
storing and shipping fuels between
refineries, pipelines, terminals, and
retail locations. These unique fuels
decrease nationwide fungibility of
gasoline, which can lead to local supply
problems and amplify price
fluctuations.231, 232 In addition to the
existing state fuel programs, we are
aware of a number of other states
considering new programs (although in
the context of the recently enacted
Energy Policy Act it is unclear what will
occur). While the timeline for state
action on new fuel formulations could
be prior to any nationwide ultra-low
sulfur standard, implementation of such
a standard could help diminish issues
related to small-market fuel programs in
the long term.
From the perspective of gasoline
production, reducing sulfur to ultra-low
levels does not happen completely
independently of other fuel parameters.
The emissions benefits of further sulfur
reduction gained in vehicle
aftertreatment may be offset by
unintended changes in other gasoline
properties. The refining process
modifications required to bring sulfur to
ultra-low levels begin to have a stronger
effect on other components of gasoline,
such as olefins (the effect of which is
discussed in the previous section).
These impacts must be further evaluated
before moving forward with a proposal
of additional sulfur reductions for the
purpose of air toxics reduction. These
issues are also discussed in more detail
in Chapter 6 of the RIA.
Refiners with whom we have met
have generally expressed disapproval of
further sulfur control. The Tier 2
gasoline sulfur program requires refiners
to meet an average standard of 30 ppm.
In response many have invested in and
brought online desulfurization units,
which would not have the capacity to
230 These changes have focused almost
exclusively on additional RVP control, with just
one program also controlling sulfur to 30 ppm
earlier than required by EPA.
231 EPA, Study of Unique Gasoline Fuel Blends
(‘‘Boutique Fuels’’), Effects on Fuel Supply and
Distribution and Potential Improvements, EPA420–
P–01–004
232 GAO, Special Gasoline Blends Reduce
Emissions and Improve Air Quality, but Complicate
Supply and Contribute to Higher Prices, GAO–05–
421
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reach a new, lower standard of 10 ppm
in many cases. Modifications would
have to be made to units that have
recently been installed to comply with
the current gasoline sulfur
requirements. In some cases these units
might have to be replaced with new
units. EPA requests comments on the
magnitude of the impact of a new, lower
sulfur standard, including the potential
effect on refiners that have recently
installed desulfurization units.
On the automotive side, sulfur
reduction may encourage further
development of lean-burn or directinjection gasoline technology. Leaner
combustion of gasoline results in greater
fuel economy and less VOC and carbon
dioxide emissions, but generally
produces more engine-out nitrogen
oxides. Reducing fuel sulfur to 10 ppm
would improve feasibility and reduce
cost of next-generation aftertreatment
designed to control these higher levels
of nitrogen oxides. EPA will continue to
evaluate further gasoline sulfur
reductions, and seeks comment on it,
especially with data supporting or
opposing such action.
ii. Gasoline Vapor Pressure
According to the Complex Model and
the MOBILE model, reducing fuel vapor
pressure reduces evaporative as well as
exhaust VOC emissions. Reducing VOC
emissions in turn reduces MSAT
emissions. A portion of this MSAT
emission decrease through VOC control
would likely be offset through an
increase in the relative concentration of
MSAT emissions. As volatility is
decreased, non-aromatic compounds are
removed from the gasoline, increasing
the concentration of aromatics.
Furthermore, these non-aromatic
compounds are higher in octane, which
would have to be offset—perhaps with
still further increases in aromatics. Such
increases in aromatics would lead to an
increase in the relative concentration of
benzene in VOC emissions. However,
since changing vapor pressure has an
effect on evaporative emissions,
reducing vapor pressure can also reduce
evaporative benzene from stationary
sources related to gasoline distribution
and marketing. Moreover, reducing
overall VOC emissions reduces ground
level ozone in urban areas, which itself
has a significant impact on health and
welfare.
Currently, in reformulated gasoline
(RFG) areas, fuel is limited to roughly
7.0 psi Reid vapor pressure (RVP) in the
summer season in order to meet the
VOC performance standard. Additional
vapor pressure controls considered for
this proposal would regulate RVP levels
to 7.0 or 7.8 in some conventional
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gasoline (CG) ozone nonattainment
areas, resulting in an impacted volume
of gasoline equal to about 50% of that
of current federal RFG. Further details
of these analyses are covered in Chapter
6 of the RIA.
As with the sulfur analyses above,
EPA also uses the Complex Model and
MOBILE to estimate emissions impacts
of changes in gasoline vapor pressure. In
terms of the fuel parameter itself, this
process is somewhat simpler than
modeling sulfur effects since the range
of vapor pressures useful in
conventional vehicles has been welldefined for a number of years and is not
expected to change. However, parallel to
the arguments made above for sulfur,
data on the effects of RVP changes on
air toxics in these models is dated and
does not represent newest technology.
Since our models do not reflect
improvements in emissions control
technology for the Tier 2 program, more
fuel effects studies must be carried out
before making decisions on further
gasoline vapor pressure controls. The
cooperative test program between EPA
and the Alliance of Automobile
Manufacturers described above is also
examining some of the effects of
changes in RVP.
Looking beyond emissions benefits,
more stringent national vapor pressure
standards could also help avoid
additional small market (‘‘boutique’’)
fuels. Several states and localities have
adopted their own seasonal
requirements for vapor pressure in an
effort to improve air quality,
contributing to constraints on gasoline
supply and potential for price
volatility.233 234
Feedback from refiners on further
volatility control has highlighted
concerns with the summer-winter
butane balance and resulting potentially
adverse supply implications. Currently,
refiners who produce large quantities of
RFG must remove a significant amount
of the light-end components from their
fuel in the summer to meet the vapor
pressure specifications. These light
components, primarily butanes, are
often stored and then blended back into
gasoline in the winter when higher fuel
vapor pressures are needed for
drivability reasons. Several refiners
have indicated that a new rule adding
a number of reduced RVP areas would
cause the amount of butanes removed in
233 EPA, Study of Unique Gasoline Fuel Blends
(‘‘Boutique Fuels’’), Effects on Fuel Supply and
Distribution and Potential Improvement, EPA420–
P–01–004.
234 GAO, Special Gasoline Blends Reduce
Emissions and Improve Air Quality, but Complicate
Supply and Contribute to Higher Prices, GAO–05–
421.
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summer to exceed what is useable in
winter, resulting in a net loss of volume
from the annual pool and a need to
make up supply at additional expense.
EPA will continue to evaluate further
gasoline volatility reductions, and seeks
comment on it, especially with data
supporting or opposing such action.
c. Toxics Performance Standard
While we are not proposing it, we
considered and are seeking comment on
the merits of expressing the standard as
an air toxics performance standard
rather than as a benzene content
standard. Such a standard would be
analogous to the current MSAT1
standard, but more stringent and with
an ABT component. In theory, a toxics
performance standard could provide
broader environmental benefits by
addressing other toxics in addition to
benzene. However, because controlling
benzene is more cost-effective than
controlling emissions of other MSATs,
refiners are unlikely to reduce emissions
of other MSATs whether or not the
standard is in the form of a toxics
performance standard or a benzene
content standard. Setting a toxics
performance standard at an appropriate
level also requires us to predict future
changes in fuel properties in addition to
benzene, and to be able to establish as
precisely as possible the effects of those
fuel properties on emissions of several
MSATs. In addition, a toxics emission
performance standard is more complex
to implement and enforce than a
benzene content standard. For all of
these reasons, as discussed more fully
below, we believe a benzene content
standard offers more certain
environmental results and less
complexity. However, we seek comment
on the overall merits of an air toxics
performance standard, including
comments specifically on the tradeoff
between the complexity of complying
with a performance standard and the
additional environmental benefits it
could provide.
Based on our analysis for this
proposal, fuel benzene control is by far
the most effective and cost-effective
means of achieving MSAT emission
reductions. This is consistent with our
experience with the MSAT1 and other
air toxics control programs, which have
shown that even when refiners have the
flexibility to choose among different
fuel changes to achieve MSAT control,
reduction in benzene content is the
predominant choice. Only when other
fuel changes that impact MSAT
emission performance are mandated
(e.g., sulfur control, oxygenate use) have
refiners made fuel changes other than
benzene content to control MSAT
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emissions. As a result, even if we were
to express the proposed standard as an
air toxics performance standard rather
than a benzene content standard, we
would expect the outcome to be the
same—benzene content control with
corresponding benzene emission
reductions and no changes in other
MSAT emissions. Our analysis of the
feasibility and cost of the program
would be identical as well. If future fuel
parameters are significantly different
than we have projected in this analysis
such that emissions of other MSATs
decrease, then a toxic performance
standard would result in less benzene
control than would be achieved by the
benzene content standard we propose
today, with a corresponding overall
reduction in cost. If future fuel
parameters are significantly different
such that emissions of other MSATs
increase, then refiners would need to
reduce benzene content to levels that
are not feasible considering cost, but
overall toxics performance would be
maintained.
If we were to set an air toxics
performance standard, the accuracy of
the model used in estimating the real
world effects of the many different fuel
parameters on MSAT emissions also
becomes of critical importance. To the
extent fuel changes are projected to
result in air toxics emission reductions
that are not in fact borne out in-use,
then the standard will have less benefit.
There was a great deal of work done in
the early 1990’s to develop the Complex
Model for the reformulated gasoline
program. It estimates VOC, NOX, and
certain MSAT emissions (benzene, 1,3butadiene, formaldehyde, acetaldehyde,
and POM) as a function of eight fuel
properties (RVP, oxygen, aromatics,
benzene, olefins, sulfur, E200, and
E300) for 1990 technology vehicles.
However, a similar set of comprehensive
data does not yet exist for new Tier 2
vehicles. Some of the fuel effects that
were found to be statistically significant
in the Complex Model may not be
significant for Tier 2 vehicles (e.g.,
distillation properties). Others that
impacted MSAT emissions primarily
through their impact on VOC emissions
may be of much less importance, due to
the much lower VOC emissions of Tier
2 vehicles.235 To the extent that the
Complex Model gives air toxics credit
for fuel changes that are later found to
be much smaller or not valid at all, a
toxics performance standard could
result in less fuel benzene control and
less in-use MSAT control. Of all the fuel
changes from past modeling, we would
have the greatest confidence that the
benzene relationships are unlikely to
change significantly. This is due to the
direct relationship between benzene
fuel content and benzene evaporative
and exhaust emissions, and due to the
magnitude of these impacts. Thus, we
would have the greatest confidence that
the MSAT emission reductions
projected from a fuel benzene content
standard will be realized in-use.
In addition, if we were to set an air
toxics performance standard, it would
be important to have a clear
understanding of the changes in fuel
properties anticipated in the future
independent of today’s proposal.
Significant changes in the composition
of gasoline are anticipated over the next
several years as a result of the Energy
Policy Act of 2005 (EPAct). MTBE is
being removed from gasoline, ethanol
use is increasing dramatically, and the
oxygenate mandate for RFG is being
eliminated. To the extent that these
changes would result in reductions in
modeled MSAT emission performance
automatically, then refiners could
comply with an air toxics performance
standard with less benzene control than
would be achieved under today’s
proposed benzene standard, and with
lower overall costs. Conversely, to the
extent that these changes would result
in increases in modeled MSAT emission
performance, an air toxics performance
standard would require refiners to take
additional measures to maintain overall
MSAT performance, but these measures
may not be cost-effective.
Although a toxics performance
standard could theoretically give
refiners more flexibility than a program
focusing only on benzene emissions, we
do not believe that such flexibility
would be meaningful in actual practice.
As discussed above, in order to comply
with a new total MSAT standard, we
expect that refiners would rely almost
exclusively on benzene control.
However, if their emission performance
for other MSATs changed in the future
(due to such factors as changes in
oxygenate use, octane needs, or crude
oil quality), refiners could find
themselves unable to maintain overall
MSAT performance using cost-effective
controls.
For all these reasons, we are not
proposing to address fuel-related MSAT
emissions with a toxics performance
standard, but we seek comment on this
option.236 We also seek comment on the
236 As
235 This is one reason why the Energy Policy Act
of 2005 requires EPA to create an updated gasoline
emissions model by 2009.
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explained further in section VII.C.5 below,
based on the use of the currently available models,
the proposed rule would result in greater overall
reduction of air toxics from all gasoline than the
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merits of applying an air toxics
performance standard in addition to a
fuel benzene content standard, and how
such a dual standard could be
implemented. From a theoretical
standpoint, this dual standard might
serve as a backstop to ensure overall
toxics performance is maintained.
However, it is not clear how such an
approach could be realistically
implemented, especially in the context
of ABT programs that apply to both.
d. Diesel Fuel Changes
We are also not proposing today to
reduce MSATs by changing diesel fuel.
The existing major diesel fuel sulfur
programs being implemented in the next
few years for highway and nonroad
diesel fuel will have a very large impact
on reducing MSAT emissions ‘‘
specifically diesel particulate matter
and exhaust organic gases. We have
found in the on-highway diesel engine
rulemaking that these are the greatest
reductions achievable and reiterate that
finding here. (See also section V.D.1.f
above.) We are not aware of other
changes to diesel fuel that could have a
significant effect on emissions of any
other MSATs. We welcome comment on
our decision to focus this proposed
program exclusively on changes to
gasoline.
2. Why Are We Proposing To Control
Benzene Emissions By Controlling
Gasoline Benzene Content?
In the previous section, we describe
how we decided to focus today’s
proposed fuel program on gasoline
benzene emissions. This section
describes our decision to propose to
reduce benzene emissions through a
gasoline benzene content standard. We
also describe our consideration of two
other potential approaches to reducing
benzene emissions, both of which
would indirectly reduce gasoline
benzene content: a standard to control
the gasoline content of all aromatic
compounds; and a standard to control
benzene emissions.
a. Benzene Content Standard
For several reasons we have decided
that a benzene content standard would
be the most cost-effective and most
certain way to reduce gasoline benzene
emissions (and thereby MSAT
emissions in general). First, a small
change in gasoline benzene content
results in large reductions in benzene
emissions ‘‘ benzene typically
current MSAT 1 program, and (consistent with
section 1504(b)(2) of the EPact) greater overall
reductions of air toxics from reformulated gasoline
than would be obtained under amended section
211(k)(1)(B) as well.
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represents around 1 percent of gasoline,
but this contributes about 25 percent of
benzene exhaust and evaporative
emissions.237 Second, we have high
confidence in the benzene emission
reductions that would result from fuel
benzene control. Historical data across a
range of vehicles and engine types
continues to support the relationship
between fuel benzene content and
benzene emissions. Even if Tier 2
vehicles react differently, the
relationship is unlikely to change
significantly. Third, because a relatively
small change in gasoline properties is
needed to achieve the desired result,
reducing benzene content does not have
a large impact on octane value. Benzene
itself does contribute to the octane value
of gasoline, but the small loss of octane
from reducing benzene content is much
less than the octane loss from reducing
other aromatics for the same benzene
emission effect, as discussed below, and
the consequences of refiners having to
replace that octane value are also much
less. (This is why, as noted earlier, we
anticipate that refiners would seek to
comply with any toxics standard by
reducing benzene levels in any case.)
Fourth, we believe that a direct benzene
content standard would best ensure real
benzene emission reductions, including
both exhaust and evaporative benzene
emissions. We discuss this conclusion
below, in the context of the potential
alternative of a benzene emission
standard.
b. Gasoline Aromatics Content Standard
Because benzene emissions are
formed from benzene and other
aromatics that are present in gasoline,
we considered a standard that would
limit the aromatics content of gasoline.
However, we believe that reducing
benzene emissions through a more
general reduction in gasoline aromatics
content would be much less costeffective than direct benzene reduction.
Non-benzene aromatics account for on
average about 30 percent of gasoline
(typically ranging between about 20
percent and 40 percent), and this
fraction contributes about 30 percent of
benzene emissions. In contrast, benzene
only makes up about 1 percent of
gasoline but is responsible for about 25
percent of benzene emissions. The
remaining benzene emissions are
formed from other compounds. Based
on the Complex Model, it would require
about a 20 percent reduction in nonbenzene aromatics to achieve the same
benzene emission reductions as the
proposed benzene content standard. As
we discussed earlier, a major
237 Based
on the Complex Model.
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consequence of removing a significant
amount of the aromatics in gasoline is
the need to replace the large loss in
octane value. As a result, it is much
more costly for refiners to reduce
benzene emissions through aromatics
control than through benzene control.
We have not evaluated the cost of
aromatics control recently, but when we
did so for the RFG rule in the early
1990s, the cost was about 5 times more
to achieve the same benzene reduction
through aromatics control than through
benzene control.238 In recent years a
variety of factors have reduced the use
of MTBE as an octane booster; we
expect that this trend will raise the
relative cost of aromatics control even
further.
In addition, aromatics reductions
would have to be offset with other highoctane compounds, such as ethanol and
ethers (e.g., ETBE and MTBE).
Increasing other high-octane
compounds tends to significantly
increase other air toxics emissions (like
acetaldehyde or formaldehyde).
Consequently, the benzene emission
reductions would be substantially offset
by increases in other toxics. For these
reasons, aromatics control has
historically only been cost-effective for
refiners when other requirements are
placed on them, such as state or federal
oxygenate mandates that also serve to
boost octane value. For this same
reason, we anticipate that further
aromatics reductions will occur as a
result of the near doubling of the use of
ethanol in gasoline due to the renewable
fuels standard contained in the EPAct.
Given a mandate for ethanol use and the
cost associated with it, refiners can
reduce their refining costs by further
reducing aromatics.
Aromatics control would also affect
other recent fuel control programs. For
example, many refineries depend on the
reforming process that produces
aromatics to also supply much or all of
the hydrogen needed for gasoline and
diesel desulfurization processes.
Reducing aromatics thus would
indirectly reduce hydrogen supply,
which would then likely require refiners
to either purchase hydrogen or build
hydrogen production facilities.
At the same time, although it would
not be constrained, we do not believe
that in the absence of aromatics control,
refiners would be likely to increase
gasoline aromatics content in the future.
Aromatics are a relatively valuable
gasoline component, and refiners are
generally careful not to make changes
238 Final Regulatory Impact Analysis for
Reformulated Gasoline, AEPA420–R–93–017,
December 1993.
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that would increase aromatics content
more than is needed for octane
purposes. In addition, as mentioned
previously, the Renewable Fuel
Standard that will be promulgated
under the new Energy Policy Act will,
by boosting ethanol use, increase the
octane of the gasoline pool. We expect
that this, in turn, will prompt refiners to
reduce their use of aromatics for octane
enhancement. Also, higher gasoline
prices recently have reduced the
demand for premium grade gasoline,
which generally has higher aromatics
levels. To the extent that this trend
continues, we expect that it will tend to
further reduce the levels of aromatics in
the overall gasoline pool.
For all of these reasons, we believe
that reducing benzene emissions
through a benzene content standard
would be much superior to doing so
through an aromatics content standard.
However, there may be other benefits
associated with aromatics control in
addition to benzene emissions. EPA is
working to improve its understanding of
the effect of mobile source emissions on
ambient PM, especially secondary PM.
For example, there is limited data that
suggest that aromatic compounds
(toluene, xylene, and benzene) react
photochemically in the atmosphere to
form secondary particulate matter (in
the form of secondary organic aerosol
(SOA)), although our current modeling
tools do not fully reflect this. One caveat
regarding this work is that a large
number of gaseous hydrocarbons
emitted into the atmosphere having the
potential to form SOA have not yet been
studied in this way. It is possible that
hydrocarbons which have not yet been
studied produce some of the SOA
species which are being used as tracers
for other gaseous hydrocarbons. This
means that the current interpretation of
the available studies may over-estimate
the amount of SOA formation in the
atmosphere. We seek comment on the
potential benefits, costs, and other
implications of aromatics control for
consideration in the future.
c. Benzene Emission Standard
In addition to the benzene or
aromatics fuel content standards
discussed above, we have considered
reducing benzene emissions through a
benzene emission standard. The
primary argument for such an approach
is that it would focus on the
environmental outcome we are
interested in ‘‘ reduced benzene
emissions ‘‘ while providing refiners
some flexibility in how that goal was
met.
In order to fully discuss this option,
it is useful to clarify how such a
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benzene emission standard would be
implemented. Instead of directly
measuring gasoline content to determine
compliance, as would be the case with
a benzene (or aromatics) content
standard, compliance would be
determined using EPA’s Complex Model
or an updated version of it. Several
parameters of a refiner’s gasoline
(including benzene and aromatics
content) would be used as inputs into
the model. Based on these and other
assumed properties of the gasoline, the
model would estimate the expected
level of benzene emissions from that
gasoline formulation.
As compared to a program based on
the direct measurement of benzene
content in gasoline, we believe that one
relying on modeled estimates of
benzene emissions would be difficult to
set today. As with the toxics
performance standard we considered
above, gasoline parameters and their
effects on MSAT emissions will be
changing in the future due to the Energy
Policy Act, changes in crude oil
supplies, and perhaps other unknown
factors. In addition, the effects of fuel
changes on MSAT emissions from the
new Tier 2 vehicles now entering the
light-duty fleet are poorly represented in
our modeling. Thus, it would be
difficult to accurately predict future
gasoline parameters and set an
appropriate benzene emission standard
that ensured the greatest emission
reduction achievable, especially a
standard that could remain stable for a
number of years. As benzene content
has been and is sure to remain by far the
most important fuel parameter in
estimating benzene emissions, a
benzene content standard provides
greater assurance of actual benzene
emission reduction in-use.
Even if it were practical to set a longterm benzene emission standard, such
an approach would be problematic for
other reasons. As we have stated, the
only significant option for reducing
benzene emissions other than reducing
benzene content is reducing aromatics
content. Since we do not believe that
requiring control of gasoline aromatics
is appropriate at this time, a benzene
emission standard would not result in
appreciably different emission
reductions than would result from a
benzene content standard. However,
given that aromatics control is a less
effective means of reducing benzene
emissions and has a more disruptive
effect on octane values (as just
discussed), requiring more aromatics
control could dramatically increase the
cost of compliance. Finally, although a
benzene emission standard might be
assumed to offer additional flexibility to
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refiners, we do not believe that such
flexibility would actually exist. Faced
with a dependence on aromatics to meet
octane requirements, and in some cases
to provide hydrogen supply for
desulfurization of gasoline and diesel
fuel, we believe that refiners would
choose benzene content reduction over
aromatics reductions even when they
theoretically had the choice to do
otherwise. Experience with the MSAT1
emissions performance standard has
confirmed this. However, as mentioned
previously, gasoline parameters do
change, octane requirements can
decrease, ethanol will supply additional
octane, and therefore aromatic
reductions may occur in the future
regardless. Were this to occur, a benzene
emission standard set today could allow
benzene content to increase in the
future. Given the additional complexity
and uncertainty associated with a
benzene emission standard, we have
therefore elected to propose a benzene
content standard exclusively. We
request comment on this approach and
on a benzene emission standard.
3. How Did We Select the Level of the
Proposed Gasoline Benzene Content
Standard?
a. Current Gasoline Benzene Levels
In selecting an appropriate level for
the proposed benzene content standard,
we began by evaluating the current
status of the industry regarding gasoline
benzene. Benzene content varies widely
among refineries, depending on such
factors as refinery configuration and
proximity to benzene markets. The
national average benzene level was 1.6
vol% in 1990. Due to the 0.95 vol%
requirement of the 1995 RFG program,
the introduction of gasoline oxygenate
requirements, and other factors, benzene
levels have since declined. By 2003,
RFG averaged 0.62 vol% benzene. (See
section V.D.1 above.)
Benzene levels have also declined for
CG over the same period, to an average
of 1.14 vol%. This is in part because
when faced with investing in new
processes to comply with the RFG
benzene standard, some refiners found
it economical to install more benzene
extraction capacity than was needed to
meet the standard. As a result, in many
cases, these refiners have also controlled
benzene from CG.
b. The Need for an Average Benzene
Standard
Even before considering the level of
the benzene content standard, we first
needed to consider the standard’s
potential form. A standard for this
purpose could be expressed as a per-
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gallon benzene limit, which would
ensure that no gasoline exceeded a
specified benzene level. In contrast, a
benzene content standard could be
expressed as a flexible average level,
allowing some of the existing variability
in current benzene levels to remain
while reducing overall benzene levels.
For several reasons, it became clear that
an average standard was the most
appropriate for this program.
As mentioned above, there is a great
diversity in the benzene content of
gasoline currently produced at refineries
across the country. In 2003, the annual
average benzene content of refineries
ranged nationally from under 0.5 vol%
to above 3.5 vol%. This variation among
refineries is also reflected in large
regional differences in average gasoline
benzene content, as illustrated below
(Tables VII.C–2 and VII.F–1).
In addition to average benzene levels
varying widely across refineries and
regions, per-gallon benzene levels for
individual batches produced by a
refinery also vary dramatically
depending on the crude oil supply and
the refinery streams used to produce a
particular batch. This variation occurs
as a result of a wide range of day-to-day
decisions necessary in producing
marketable gasoline within a refinery on
a continuous basis. We reviewed actual
batch data for a typical refinery
producing both RFG and CG with an
average benzene content of 1.6 vol% for
all its gasoline, and batch benzene levels
ranged from under 0.1 to 3.0 vol% for
CG. The range for RFG is typically
narrower due to the existing 1.3 vol%
per gallon cap, but still shows
significant batch to batch fluctuations.
Batches that refiners produce with
benzene higher than 1.3 vol% are
marketed as CG.
We considered controlling benzene
emissions with a fixed, per-gallon
benzene content standard to be met at
all refineries. By capping gasoline
benzene content in this way, the
program would ensure that all gasoline
nationwide would have benzene levels
below the selected upper limit.
However, as we developed the rule, it
became clear that with the large
variation in benzene levels among
refineries and regions (reflecting the
variation in the economics of reducing
benzene), a per-gallon standard would
have to be so high (to account for
maximum, legitimate potential
variability) as to leave most refineries
with little or no need to reduce benzene.
Moreover, the burden of the national
control program would fall almost
entirely on the refineries where the
challenges of control would be greatest,
and where the most lead time would be
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required for compliance. With many
refineries able to comply without
making any changes, we do not believe
such a program would represent the
greatest reduction feasible, as the Clean
Air Act requires.
The typical fluctuations in benzene
content among batches at individual
refineries, as discussed above, also
indicate the need for refiners to have a
degree of flexibility in producing
gasoline, as would be provided by an
average benzene standard. Restrictions
on day-to-day fluctuations would not
significantly affect average benzene
levels, but would certainly increase
costs as refiners invested in avoiding
occasionally higher benzene batches.
We believe that allowing refiners to
average batches with fluctuating
benzene over a year’s time, as we
propose, would result in a more costeffective program.
Most importantly, it is clear that with
the incorporation of a carefullydesigned benzene credit averaging,
banking, and trading (ABT) program, a
more stringent benzene standard would
be feasible, and implementation could
occur earlier. Thus, we are proposing a
0.62 vol% annual average standard to
begin in 2011. Under the proposed ABT
program, refiners could generate early
credits by making early reduction efforts
prior to 2011. Refiners would have an
incentive to do so, because the credits
generated could be used to postpone
more expensive final investments in
benzene control technology. In this way,
the ABT program would allow the
economic burden of the benzene
standard to be more efficiently
distributed among refiners and over
time. The proposed ABT program would
result in lower benzene levels in all
areas of the country compared to today’s
levels, as described in more detail below
in section VII.D.
c. Potential Levels for the Average
Benzene Standard
We evaluated a range of potential
standards on a national refinery annual
average basis from 0.52 to 0.95 vol%
benzene.239 Our refinery-by-refinery
model incorporates data on individual
refineries whenever possible and
estimates the likely technological
approaches that refiners would choose
for each refinery to comply with each
potential standard at the least cost. The
model chooses among several
technological options that are the most
common and effective methods
available to refiners to reduce gasoline
239 For this evaluation we used both refinery
linear programming (LP) models and a refinery-byrefinery model developed specifically for this rule.
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benzene content. (Section VII.F below
and Chapter 6 of the RIA have more
detailed discussions of benzene
reduction technologies).
All of the methods that we considered
focus on reducing benzene content in
the reformate stream, which is the
product of the reformer unit. The role of
the reformer unit is to increase gasoline
octane, which it does by generating
aromatic compounds from simpler
hydrocarbons. Benzene is one of the
aromatic compounds produced by the
reformer. Reformate accounts for 30–
40% of gasoline volume and can contain
as much as 12% benzene. As a result,
reformate contributes the majority of the
total benzene content of gasoline. For
these reasons, treatment of reformate is
usually the most effective and
economical means of reducing benzene
content. Several proven and
commercially available technologies
exist for reducing benzene creation in
the reformer and removing it from the
reformate product.
The least stringent standard we
evaluated, a national average of 0.95
vol% benzene, would not require any
changes at most refineries. For the
refineries where action would be
needed, we project that most could be
brought into compliance by reducing
creation of benzene in the reformer
using the simplest and least costly of the
technology options evaluated. We do
not believe that a standard at this level
would meet the statutory requirements
of section 202(l) of the Clean Air Act to
achieve the greatest reductions
achievable considering cost and other
factors since, as discussed below,
greater reductions are feasible at
reasonable cost, and without adverse
energy or safety implications.
As the most stringent case, we
evaluated a national average benzene
content standard of 0.52 vol%. Our
analysis indicates that a standard at this
level would require all refiners to invest
in the most effective technologies used
today that remove the benzene from
their reformate product streams
(benzene saturation and benzene
extraction, as discussed below). If the
ABT program were fully utilized (all
credits generated were used), we believe
all refiners might comply with this
average standard. Because of the almost
universal need for refineries to use the
most expensive reformate-based
benzene control technologies, we
believe a standard of 0.52 vol% would
be very challenging economically for
many refineries, and we believe that
such a standard would not be
achievable taking costs into
consideration, as we are required to do
under section 202(l). In addition, if, as
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appears likely, ‘‘perfect’’ credit trading
did not occur, some refiners would have
to use additional, more extreme
approaches that would be even more
costly and would require more difficult
compromises in the operation of the
refineries. (We discuss these
technological and operational
approaches to benzene reduction in
more detail in section VII.F below and
in Chapter 6 of the RIA.)
In 2003, the average benzene level in
RFG was 0.62 vol%.240 We believe an
annual average benzene standard of 0.62
vol% applied to all gasoline (both CG
and RFG) would be feasible considering
cost and other factors. Furthermore,
implementing an average benzene
standard of 0.62 vol% would achieve
several other important program goals.
At this level, the same benzene standard
could be applied to both RFG and CG
nationwide, and our analysis shows that
the RFG benzene reductions already
achieved by the industry to date would
not be lost. We expect that refiners
currently producing RFG with benzene
levels below 0.62 vol% would continue
to be committed to producing lowbenzene gasoline based on prior
investment in benzene extraction
equipment or ABT credit incentives.
Additionally, as discussed below in
VII.C.5, a gasoline benzene standard of
0.62 vol% would achieve sufficient
mobile source air toxic reductions
allowing this program to supersede the
additional MSAT requirements under
EPAct. Finally, an average benzene
standard applied to both CG and RFG,
would allow for a uniform nationwide
ABT program providing additional
flexibility and reduced compliance costs
to refiners, resulting in the greatest
achievable reductions within the
meaning of section 202(l).
At a national average standard of 0.62
vol%, we estimate that a number of
refiners would produce gasoline with
significantly lower fuel benzene levels,
creating enough benzene credits to
allow refiners in less economically
favorable positions to purchase these
credits on an on-going basis and use
them for compliance purposes. We
project that further reductions would
occur not only in CG, but also in RFG,
despite the fact that RFG is already
averaging 0.62 vol%. As discussed in
section IX below and in Chapter 9 of the
RIA, as the stringency is pushed below
0.62 vol%, the overall program costs
would begin to rise more steeply. This
is because in meeting a lower average
standard, there would be fewer
240 Volume-weighted average benzene level based
on January 1, 2003 to December 31, 2004 RFG batch
reports.
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refineries able to comply at low cost,
resulting in fewer credits being
generated. This in turn would require
more investment among refiners with
higher costs of compliance.
We also considered a program that
would apply separate benzene content
standards to RFG and CG. In the context
of any nationwide ABT program that
allowed trading across both RFG and
CG, separate standards for these two
gasoline pools would not be
fundamentally different from the
proposed unified standard. The only
impact would be to somewhat change
which refiners generated credits and
which used credits, and to what degree.
For separate RFG and CG standards to
have a meaningful impact in
comparison to today’s proposed
program, separate trading programs for
each of the two gasoline pools would be
required. Our modeling shows that
without the credits generated by RFG
producers in a nationwide trading
program, it would not be possible to set
as stringent a standard for CG. The
higher-benzene refineries that would
most need credits to meet a stringent
average standard are a subset of
refineries that produce CG. As a result,
in a program with separate RFG and CG
pools, we would expect to set a slightly
more stringent standard for RFG alone,
but we would need to set a substantially
relaxed standard for CG. The net result
would be, at best, the same nationwide
average benzene reductions in the RFG
and CG pools that would be expected
under a unified standard. However,
there would be a clear risk that the
reduced generation of credits by lowercost refineries would lead to either a
significant increase in the cost of the
program (because higher-cost refineries
would need to make refinery changes
earlier) or the potential for fewer
reductions through the process of
setting the levels for the separate CG
and RFG standards. Conversely, with a
unified standard and nationwide ABT,
we believe that the program would
achieve the maximum economical
reduction in all areas and greater overall
benzene reduction over the CG and RFG
pools.
In addition, we considered a
somewhat less stringent national
average standard than the proposed 0.62
vol% (e.g., 0.65 or 0.70 vol%). Such
standards would still achieve significant
benzene emission reductions. However,
we are concerned that a less stringent
standard would not satisfy our statutory
obligation for the most stringent
standard feasible considering cost and
other factors. Furthermore, such
standards would not allow us to
accomplish several important
programmatic objectives. Given that the
average benzene content of RFG in 2003
was already 0.62 vol%, such higher
standards would not provide the
certainty that the air toxics performance
of RFG would decline in the future. This
would then trigger the provisions in the
2005 EPAct to adjust the MSAT1
baseline for RFG. The only way of
avoiding this situation would be to
maintain separate standards for RFG
and CG where the RFG standard was
still more stringent than 0.62 vol% and
credits could not be used from CG to
comply. As discussed above, having
separate standards with separate ABT
programs raises additional cost and
feasibility issues.
For all of the above reasons, we
believe that a refinery annual average
benzene content standard of 0.62 vol%
applying to all gasoline nationwide
(excluding California), in conjunction
with an appropriately-designed ABT
system, would maximize benzene
emission reductions considering cost
and other factors.
Section 202(l)(2) also requires that we
consider lead time in determining the
greatest reductions achievable. We are
proposing that the standard of 0.62
vol% become effective on January 1,
2011. Because the final rule will be
completed in early 2007, this would
allow about 4 years for refiners to plan
and execute the necessary capital
projects and operational changes needed
to meet the program requirements. We
discuss our assessment of necessary
lead time in section VII.F below. We
believe that this proposed level for the
standard, the proposed ABT program,
and the proposed implementation date
together meet the statutory requirement
that the program results in the greatest
emission reduction achievable
considering costs and other factors.
We encourage comment on our
selection of this level for the standard,
especially with data and analysis that
support the comments.
d. Comparison of Other Benzene
Regulatory Programs
In addition to the benzene content
standard of the RFG program, California
and several countries have regulatory
limits on the benzene content of
gasoline. Table VII.C–1 shows the basic
provisions of each of these programs.
Canada has limits similar to those
covering U.S. RFG. In Canada,
producers may either comply with a 1.0
vol% flat limit or an averaging standard
of 0.95 vol%, with a per-gallon cap of
1.5 vol%. The European Union regulates
fuel to the same level in all its member
countries, currently a per-gallon cap of
1.0 vol%. Japan has the same limit as
the E.U., while South Korea will be
moving from a cap of 1.5 to 1.0 vol%
in 2006.
California is the only state that has
implemented a benzene standard, and it
is similar to the standard we are
proposing today. California’s average
standard is 0.7 vol%, with a per-gallon
cap of 1.1 vol%. Together, these
standards result in an average 0.62 vol%
in-use gasoline benzene level.
TABLE VII.C–1.—OTHER GASOLINE BENZENE CONTROL PROGRAMS
Federal RFG
Average Std (vol%) ..................................
Per-gallon Cap (vol%) ..............................
California
phase 3 RFG
0.95 a
1.3
Canada
0.7
1.1
0.95
1.5
South Korea
Japan
European
Union
........................
1.5 b
........................
1.0
........................
1.0
a Producers
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b Limit
may also comply with a per-gallon cap of 1.0.
to be lowered to 1.0 in 2006.
4. How Do We Address Variations in
Refinery Benzene Levels?
a. Overall Reduction in Benzene Level
and Variation
As explained above, there is currently
a wide variation in gasoline benzene
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levels across the country. According to
summer 2003 batch data (proposed
baseline 241), average benzene content
241 For
the purpose of our analyses, we selected
2003 to represent current (baseline) conditions
because it reflected the most recent batch data
available. The refinery-by-refinery model used to
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ranged from 0.41 to 3.81 vol%,
including both RFG and CG. The current
predict refinery behavior (discussed later in section
IX) is based on inputs from the linear programming
(LP) model, which is set up to only model the
summer season. As a result, we have used summer
2003 as our baseline period.
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variation in benzene levels is primarily
attributable to differences in crude oil
quality, different refinery
configurations, and differences in
refinery operations. Our analysis of the
proposed program, summarized below,
concludes that average benzene levels
would be reduced in all areas of the
country (PADDs 242) and variation
among refineries would also be reduced.
We believe that under the proposed
rule, virtually all refineries would
reduce their benzene levels and that no
refineries would increase their benzene
levels.
Upon implementation of the proposed
0.62 vol% benzene standard in 2011, we
believe that some refiners would reduce
benzene levels to below the standard
while others would reduce benzene
levels but would need to rely partially
or largely on credits generated and
traded under the proposed ABT
program, as described below. Refiners’
compliance strategies would ultimately
be driven by economics. For many it
would be economical to reduce gasoline
benzene levels to 0.62 vol% or below.
For others it would be economical to
make some reduction in gasoline
benzene levels and rely partially upon
credits. For some refineries already
below the standard, no benzene
reduction efforts would be necessary.
For the limited number of remaining
technologically-challenged refineries it
would be most economical to rely
wholly upon credits. Regardless of the
compliance strategies selected, under
the proposed program, benzene levels
and variation would be reduced
nationwide.
TABLE VII.C–2.—BENZENE LEVELS IN GASOLINE PRODUCED CURRENTLY AND UNDER THE PROPOSED PROGRAM
Number of refineries by gasoline benzene level (vol%)
<0.5
0.5–<1.0
1.0–<1.5
1.5–<2.0
2.0–<2.5
Benezene level (vol%) *
>=2.5
Min
Max
Range **
Avg ***
Starting Gasoline Benzene Levels***
PADD
PADD
PADD
PADD
PADD
1 .....................................................
2 .....................................................
3 .....................................................
4 .....................................................
5 **** ...............................................
4
0
4
0
0
3
5
18
1
0
3
8
10
4
1
0
11
7
6
3
2
1
0
3
2
0
1
2
2
2
0.41
0.60
0.41
0.60
1.36
2.19
2.85
3.10
3.56
3.81
1.77
2.25
2.69
2.96
2.44
0.62
1.32
0.86
1.60
2.06
Total ...................................................
8
27
26
27
8
7
0.41
3.81
3.39
0.97
Benzene Levels After Program Implementation
PADD
PADD
PADD
PADD
PADD
1 .....................................................
2 .....................................................
3 .....................................................
4 .....................................................
5 *** ................................................
4
1
10
0
0
5
22
27
8
4
1
1
3
7
2
2
2
0
1
2
0
0
1
0
0
0
0
0
0
0
0.41
0.49
0.36
0.53
0.54
1.96
1.95
2.07
1.94
1.84
1.54
1.46
1.71
1.40
1.30
0.51
0.73
0.55
0.95
1.04
Total ...................................................
15
66
14
7
1
0
0.36
2.07
1.71
0.62
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* Starting benzene levels based on summer 2003 batch data.
** Range in benzene level (MIN–MAX).
*** Average volume-weighted benzene level.
**** PADD 5 excluding California.
As shown in Table VII.C–2, average
benzene levels would be reduced by
36%, from 0.97 vol% (baseline) to 0.62
vol% once the program is fully
implemented. Variation in benzene
level, measured in terms of range,
would be reduced by 50% (from 3.39
vol% to 1.71 vol%). In addition the
areas with the highest starting benzene
levels and variation (PADDs 2, 3, 4 and
5) would experience the greatest
reductions.
In conclusion, we project that under
the proposed program all areas of the
country would see reductions in average
benzene level and variation among
refineries would also be reduced.
Refiners would have several motivations
for making the benzene reductions
projected by our analysis. First,
reducing actual benzene levels could be
the most economically-favorable
compliance strategy. Secondly, reducing
benzene levels would help reduce or
eliminate the uncertainty associated
with relying on credits. Finally,
reducing benzene levels could generate
credits that would be valuable to the
refining industry.
242 The Department of Energy divides the United
States into five Petroleum Administration for
Defense Districts, or PADDs. The states included in
each PADD are defined at 40 CFR 80.41.
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b. Consideration of an Upper Limit
Standard
We believe that the proposed program
would provide significant benefits in all
areas of the nation. Nevertheless, we
recognize that some commenters are
likely to be concerned that under a
flexible ABT program it is possible that
some refiners could maintain their
current benzene levels or even increase
them and comply through the use of
credits. If such a refinery dominated a
particular market, then even though
nationally there would be significant
benzene reductions, they might not
occur in that market. While our analysis
does not lead us to believe that such an
outcome would happen, we have
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nevertheless considered whether an
upper limit on benzene (in addition to
the average standard) would be valuable
to prevent that outcome from
happening.243 We considered two
different forms of an upper benzene
limit to complement the average
standard: a per-gallon cap standard and
a maximum average standard.
i. Per-Gallon Cap Standard
A cap would require that each gallon
(or batch) of gasoline produced or
imported not contain more than a
specified concentration of benzene.
Such a standard would force those
refineries with the highest benzene
levels to make physical changes to their
gasoline instead of having the option of
relying exclusively on credits. In
addition to formally limiting the
maximum benzene content sold
anywhere in the country, such a cap
would also be straightforward to enforce
243 Upper limits on benzene are a part of
comparable programs in California and in other
countries.
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at any point in the distribution system.
Note that we are proposing that the
existing per-gallon cap of 1.3 vol%
benzene would remain in effect for RFG
under this rule. EPA invites comment
on whether the RFG benzene cap should
be retained.
The primary disadvantage of adding a
rigid cap is that it would not allow for
occasional, short-term fluctuations in
benzene content. Refiners are faced with
a range of unexpected or planned
circumstances that could cause
temporary spikes in benzene content,
including equipment malfunctions and
periodic maintenance. Although the 1.3
vol% cap would remain for RFG, to
apply a cap in this range to CG would
eliminate a necessary market for higher
benzene batches.244 With no ability to
market the gasoline, the refiner would
be forced to suspend gasoline
production. This could in turn force the
shutdown of the entire refinery,
sacrificing supply of all products. To
attempt to avoid this situation, refiners
would need to invest more heavily in
benzene control than needed to meet the
average standard, simply to provide
back-up control to protect against shortterm fluctuations. For some higherbenzene refineries, a cap could make
complying with the program
prohibitively expensive.
Consequently, we concluded that if
we were to impose a per-gallon cap, it
would have to be high enough to allow
most refineries to continue to operate
even in such upset situations (in order
to account for legitimate maximum
potential daily variability), thereby
providing little overall benefit.245
Alternatively, we would have to allow
exceptions to the per-gallon cap for such
upset situations, which would be
burdensome to implement and also
result in little overall benefit.
If refiners with higher-benzene
refineries need to invest in greater
benzene control in order to protect
against unpredictable upsets, their costs
would be even higher relative to those
of lower-benzene refineries. As in the
case of a program with no ABT at all,
the statutory requirement to balance the
degree of feasible emission reduction
with cost (and other factors) would have
the counterproductive effect of requiring
a less stringent overall program.
244 As explained in section VII.C.5 below, CG
provides a limited safety valve for occasional
batches of high-benzene RFG due to the Antidumping provisions.
245 In California and other countries with benzene
control programs, the refining industry tends to be
more homogeneous than in the U.S. as a whole and
face different market situations, resulting in
different considerations regarding upper limits.
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At the same time, the per-gallon cap
would appear to provide no overall
additional reduction in benzene levels.
Despite the increased costs, particularly
for higher-benzene refiners, our analysis
indicates that little additional emission
reduction would result (primarily
because the higher-benzene refineries
represent a relatively small fraction of
nationwide gasoline production).
Instead, as discussed below, emission
reductions are expected to simply shift
from one region of the country to
another, with no change in the overall
emission reductions. Because of this,
and due to the potential deleterious cost
impacts, we are not proposing a pergallon cap benzene standard.
ii. Maximum Average Standard
Another means of ensuring some
reduction by those refiners with the
highest benzene concentrations would
be to impose a maximum average
standard. An annual maximum average
standard for each refinery would limit
the average benzene content of its actual
production over the course of the year,
regardless of the extent to which credits
may have been used for compliance.
While slightly less restrictive than a pergallon cap standard in that some
shorter-term fluctuations in benzene
levels could occur, a maximum average
standard would still limit the flexibility
otherwise available through the ABT
program. Our modeling shows that a
number of refiners would need to invest
substantially more to ensure compliance
with both the average and maximum
average standards. With the addition of
a maximum average standard, we expect
emission reductions to simply shift from
one region of the country to another
with no net change in overall emission
reductions. For example, when
analyzing a 1.3 vol% maximum average
standard, benzene levels were lowered
in two PADDs and raised in three
PADDs compared to our proposed
program yet the overall emission
reductions remained the same.246 Since
we believe that a maximum average
standard would increase costs but not
achieve any greater emission reduction,
we are not proposing such a standard.
We believe that the proposed ABT
program, in combination with the
proposed 0.62 vol% benzene standard
without a cap or maximum average
limit, would result in the maximum
feasible reduction in benzene emissions,
considering costs, energy, and safety
issues. The proposed ABT program
would provide refiners with compliance
flexibility while ensuring that the
246 This program comparison is discussed further
in Chapter 9 of the RIA (Table 9.6–7).
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national program achieves significant
overall benzene emission reductions.
We invite comment on our
conclusions about having an upper limit
in addition to an average standard.
5. How Would the Proposed Program
Meet or Exceed Related Statutory and
Regulatory Requirements?
Three fuels programs (RFG, Antidumping and MSAT1) currently contain
direct controls on the toxics
performance of gasoline.247 Based on
our analyses of the proposed program,
including the proposed ABT program,
we expect that meeting the proposed
fuel benzene content standard combined
with other fuel controls would also lead
to compliance with the toxics
requirements of all these programs.
The RFG program, implemented in
1995, contains a fuel benzene standard
that requires a refinery’s or importer’s
RFG to average no greater than 0.95
vol% benzene annually.248 In addition,
RFG has a per-gallon benzene cap of 1.3
vol%. Each refinery’s or importer’s RFG
must also achieve at least a 21.5%
annual average reduction in total toxics
emissions compared to 1990 baseline
gasoline.249 The Anti-dumping
regulations require that a refinery’s or
importer’s CG produce no more exhaust
toxics emissions on an annual average
basis than its 1990 gasoline.250 This
program keeps refiners from shifting
fuel components responsible for
elevated toxic emissions into CG as a
way to comply with the RFG standards.
Section V.D.1 above describes these
programs in more detail.
The MSAT1 program, implemented in
2002, was overlaid on the RFG and
Anti-dumping programs.251 As
explained in section V.D above, it was
not designed to further reduce MSAT
emissions, but to lock in
overcompliance on toxics performance
that was being achieved in RFG and CG
under the RFG and Anti-dumping
programs. The MSAT1 rule requires the
annual average toxics performance of a
refinery’s or importer’s gasoline to be at
least as clean as the average
performance of its gasoline during the
three-year baseline period 1998–
247 Other gasoline fuel controls, such as sulfur,
RVP or VOC performance standards, indirectly
control toxics performance by reducing overall
emissions of VOCs.
248 40 CFR 80 Subpart D. Refiners also have the
option of meeting a per gallon limit of 1.0 vol%.
249 Emissions determined using the Complex
Model, as defined in 40 CFR 80.45.
250 CFR 80 Subpart E, emissions determined using
the Complex Model.
251 40 CFR 80 Subpart J.
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2000.252 Compliance with MSAT1 is
determined separately for each
refinery’s or importer’s RFG and CG.
Today’s proposed 0.62 vol% benzene
content standard would apply to all of
a refinery’s or importer’s gasoline ‘‘ that
is, the total of its RFG and CG
production or imports. This level of
benzene control would far surpass the
RFG standard of 0.95 vol%, and would
put in place a benzene content standard
for CG for the first time.253 As described
further in Chapter 6 of the RIA, we
analyzed the expected overall toxics
performance under today’s proposed
program of benzene and vehicle
standards using currently-available
models and compared it to toxics
performance under the pre-existing
standards.254 When RFG and CG toxics
emissions are evaluated at this new
level of benzene control, it is clear that
the benzene standard proposed today
would result in the MSAT1 toxics
emissions performance requirements
being surpassed (i.e., bettered) not only
on average nationwide, but for every
PADD.255
To address compliance with statutory
requirements currently in effect through
the RFG and Anti-dumping programs,
we carried out a refinery-by-refinery
analysis of toxics emissions
performance using the Complex Model
(the same model used for determining
compliance with these programs). We
used 2003 exhaust toxics performance
for CG and 2003 total toxics
performance for RFG as benchmarks,
which are at least as stringent as the
relevant toxics performance baselines.
We applied changes to each refiner’s
fuel parameters for today’s proposed
standards and the gasoline sulfur
standard phased in this year (30 ppm
average, 80 ppm max). The results
indicate that all refineries maintained or
reduced their emissions of toxics over
2003. We expect large reductions in
sulfur for almost all refineries under the
gasoline sulfur program, and large
reductions in CG benzene levels along
with modest reductions in RFG benzene
levels. We do not expect backsliding in
sulfur levels by the few refiners
previously below 30 ppm because they
had been producing ultra-low sulfur
gasoline for reasons related to refinery
configuration. Furthermore, because of
its petrochemical value and the credit
market, we do not expect any refiners to
increase benzene content in their
gasoline.
In addition, we expect significant
changes in oxygenate blending over the
next several years, but these are very
difficult predict on a refinery-byrefinery basis. Regardless of how
individual refineries choose to blend
oxygenates in the future, we believe
their gasoline will continue to comply
with baseline requirements. This is
because all RFG is currently
overcomplying with the statutory
requirement of 21.5% annual average
toxics reductions by a significant
margin. Similarly, most CG is
overcomplying with its 1990 baselines
by a significant margin. Furthermore,
we believe most refiners currently
blending oxygenates will continue to do
so at the same or greater level into the
future.
EPA is thus proposing that upon full
implementation in 2011 the regulatory
provisions for the benzene control
program would become the single
regulatory mechanism used to
implement these RFG and Antidumping annual average toxics
requirements, replacing the current RFG
and Anti-dumping annual average
provisions. However, the 1.3 vol%
maximum benzene cap would remain in
place for RFG under 40 CFR 80.41; we
are requesting comment on the need to
retain this requirement for RFG. The
proposed benzene control program
would also replace the MSAT1
requirements.
Section 1504(b) of the Energy Policy
Act of 2005 (EPAct) requires that the
MSAT1 toxics emissions baselines for
RFG be adjusted to reflect 2001–2002
fuel qualities, which would make them
slightly more stringent than the 1998–
2000 baselines originally used in the
MSAT1 program. However, as provided
for in the Act, this action becomes
unnecessary and can be avoided if
today’s proposed program achieves
greater overall reductions of toxics
emissions from RFG (i.e., PADDs 1 and
3) than would be achieved by this
baseline year adjustment. Therefore, in
addition to comparing the proposed
standard to the current MSAT1
program, we also compared it to the
program as the standards would be
modified by the EPAct.
We performed an analysis of aggregate
toxics emissions for the relevant
baseline periods as well as for future
years with and without the proposed
program. This analysis was carried out
using MOBILE6.2 because that model
accounts for changes in the vehicle fleet,
which is important when modeling
future years. Results are shown in Table
VII.C–3. Since this modeling approach
was intended to compare emissions
from different fuels and fleet year mixes,
the emissions figures generated here are
different from those used for gasoline
compliance determination.
The first row shows mg/mi air toxics
emissions in 2002 under the MSAT1
refinery-specific baseline requirements.
The second row shows how these would
change by updating the RFG baselines to
2001–02 as specified in EPAct. Since
significant changes are expected in the
gasoline pool between 2002 and the
proposed implementation time of the
fuel standard, such as gasoline sulfur
reductions and oxygenate changes, we
decided to model a ‘‘future baseline’’ to
allow comparison with the proposed
standard at the time it would become
effective in 2011. As a result, the third
row shows the projected mg/mi
emissions in 2011 under the EPAct
baseline adjustments, but without
today’s proposed program. The large
reductions in air toxics emissions
between the EPAct baseline and this
2011 baseline are primarily due to
nationwide reduction in gasoline sulfur
content to 30 ppm average and
significant phase-in of Tier 2 vehicles
into the national fleet.
An important comparison is made
between rows three and four, where the
estimated toxics emissions under the
proposed fuel standard only are
compared to the projected emissions
without the proposed standard. The
fourth row shows small reductions for
RFG and more significant reductions for
CG with the introduction of the
proposed benzene standard in 2011. We
also evaluated the effects of the vehicle
standard also proposed today on toxics
emissions at two points in time, shown
in the last two rows of the table.
252 Emissions determined using the Complex
Model, as defined in 40 CFR 80.45.
253 Proposed program retains the 1.3 vol%
maximum benzene cap for RFG required by 40 CFR
80.41.
254 As discussed previously, the existing models
contain limited data on the impacts of fuel changes
on 2004 and later technology vehicles, making such
projections difficult. However, we do not believe
the conclusions would change for these reasons: (1)
The fuel effect changes modeled here related to
benzene, for which we expect data for new
technology vehicles to show similar trends as those
for older vehicles; (2) much of the projected change
in future emissions are due to changes in vehicles
technology, not fuel changes; and (3) for this
analysis we need only look at the relative changes,
and given the magnitude of the projected effects we
do not expect that the direction of the result would
change even if significantly different values for
absolute emissions were submitted.
255 The analysis shows an even greater benefit in
overall toxics reductions when the combined effect
of the benzene standard and the vehicle standards
are considered.
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TABLE VII.C–3.—ESTIMATED ANNUAL AVERAGE TOTAL TOXICS PERFORMANCE OF LIGHT DUTY VEHICLES IN MG/MI UNDER
CURRENT AND PROPOSED PROGRAMS a
Fleet
RFG by PADD
CG by PADD
Regulatory scenario
Year
MSAT1 Baseline b (1998–2000) ...
EPAct Baseline b (RFG: 2001–
2002) ........................................
EPAct Baseline, 2011 c ................
Proposed program, 2011 c (Fuel
standard only) ...........................
Proposed program, 2011 c (Fuel +
vehicle standards) ....................
Proposed program, 2025 c (Fuel +
vehicle standards) ....................
I
II
III
I
II
III
IV
V
2002
108
124
89
104
135
96
137
152
2002
2011
103
67
121
79
85
51
104
62
135
79
96
54
137
77
152
96
2011
66
78
50
59
74
51
71
85
2011
63
76
47
55
72
47
67
81
2025
39
46
30
35
44
31
42
50
toxics performance for this analysis includes overall emissions of 1,3-butadiene, acetaldehyde, acrolein, benzene and formaldehyde as
calculated by MOBILE6.2. Although POM appears in the Complex Model, it is not included here. However, it contributes a small and relatively
constant mass to the total toxics figure (4%), and therefore doesn’t make a significant difference in the comparisons.
b Baseline figures generated in this analysis were calculated differently from the regulatory baselines determined as part of the MSAT1 program, and are only intended to be a point of comparison for future year cases.
c Future year scenarios include (in addition to the controls proposed today, where stated) effects of the Tier 2 vehicle and gasoline sulfur
standards and vehicle fleet turnover with time, as well as rough estimates of the renewable fuels standard and the phase-out of ether blending.
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a Total
Based on these analyses, we believe
the fuel program proposed in this
notice, as well as the combined fuel and
vehicle program, would also achieve
greater overall toxics reductions than
would be achieved under the EPAct
were the RFG baseline period updated
to 2001–2002.
In summary, today’s proposed action
for fuels would fulfill several statutory
and regulatory goals related to control of
gasoline mobile source air toxics
emissions. The proposed program (in
conjunction with the proposed vehicle
standards) would meet our commitment
in the MSAT1 rulemaking to consider
further MSAT control. It would also
result in air toxics emission reductions
greater than required under all preexisting gasoline toxics programs, as
well as under the baseline adjustments
specified by the Energy Policy Act. By
designing this program to address these
separate but related goals, we would be
able to achieve a benefit in addition to
the emissions reductions: A significant
consolidation and simplification of
regulation of gasoline MSATs.
As part of today’s action, in addition
to the streamlining of toxics
requirements, we propose that the
gasoline sulfur program become the sole
regulatory mechanism used to
implement gasoline NOX requirements.
Gasoline producers are required to show
reductions from their RFG relative to the
1990 Clean Air Act baseline gasoline
NOX emissions, as determined using the
Complex Model. Conventional gasoline
must comply with Anti-dumping
individual NOX baselines for each
refinery, similar to the Anti-dumping
toxics standards. A refinery-by-refinery
NOX analysis parallel to that described
above indicated that with the final
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implementation of the gasoline sulfur
program (January 1, 2006), all gasoline
will continue to meet or exceed the NOX
requirements of the RFG and Antidumping programs.
As discussed elsewhere in this
preamble, we believe that today’s
proposed nationwide program would
achieve significant reductions in
gasoline-related benzene emissions. The
program would also have the effect of
preempting states from regulating
gasoline benzene content. The program
is proposed under Clean Air Act section
211(c), which includes preemption of
state fuel programs in section
211(c)(4).256 The existing RFG benzene
program, also authorized under section
211(c)(1), preempts states in RFG areas
from regulating benzene. Today’s
nationwide program expands this
preemption to all states except
California, which is exempt from this
preemption.
D. Description of the Proposed
Averaging, Banking, and Trading (ABT)
Program
1. Overview
As mentioned earlier, we are
proposing a specially-designed ABT
program to allow EPA to set a more
stringent nationwide gasoline benzene
standard than otherwise possible. The
proposed ABT program would allow
refiners and importers to use benzene
credits generated or obtained under the
provisions of the ABT program to
comply with the 0.62 vol% refinery
average standard in 2011 and
indefinitely thereafter. Benzene credits
could be generated by refineries that
256 See discussion of statutory authority in section
I.C. of this preamble.
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make qualifying early baseline
reductions prior to 2011 and by
refineries and importers that
overcomply with the 0.62 vol%
standard in 2011 and beyond. All
credits generated could be used
internally towards company compliance
(‘‘averaged’’), ‘‘banked’’ for future use,
and/or transferred (‘‘traded’’) to another
refiner or importer.
The majority of the ABT credit
provisions we are proposing are similar
to those offered in the gasoline sulfur
program, with a few exceptions. The
major difference is that in the proposed
program, credit use would not be
restricted by an upper limit (discussed
in VII.C.4.b above) and in fact would be
encouraged by extended credit life and
nationwide credit trading provisions.
We are able to propose a flexible ABT
program and a gradual phase-in of the
0.62 vol% benzene because there is no
corresponding vehicle standard being
proposed that is dependent on gasoline
benzene content. A program with fewer
restrictions would help ensure that the
overall proposed benzene control
program would result in the greatest
achievable benzene reductions,
considering cost and other factors.
Because of the wide variation in
current benzene levels among refineries,
we recognize that some refiners would
be better situated than others,
technologically and financially, to
respond to the proposed benzene
standard. As we discuss below, we
believe that the credit trading provisions
of the ABT program would be well
suited to moderate the financial impacts
that could otherwise occur with the
proposed benzene control program.
However, in other air quality
programs, we have used other trading
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mechanisms to address the varying
impacts of such programs on different
regulated entities. For example, in
EPA’s Acid Rain program a limited
number of ‘‘emissions allowances’’ are
allocated among entities, which can
then be banked and traded. We invite
comment on this and other alternative
credit approaches that might be
appropriate to gasoline benzene control.
The following paragraphs provide
more details on our proposed benzene
ABT program. We encourage comments
on the design elements we have
proposed for the program. If you believe
that alternative approaches would make
the program more effective, please share
your specific comments and
recommendations with us.
2. Standard Credit Generation (2011 and
Beyond)
We are proposing that standard
benzene credits could be generated by
any refinery or importer that
overcomplies with the 0.62 vol%
gasoline benzene standard on an annual
volume-weighted basis in 2011 and
beyond. For example, if in 2011 a
refinery’s annual average benzene level
was 0.52, its standard benzene credits
would be determined based on the
margin of overcompliance with the
standard (0.62¥0.52 = 0.10 vol%)
divided by 100 and multiplied by the
gallons of gasoline produced during the
2011 calendar year. The credits would
be expressed as gallons of benzene.
Likewise, if in 2012 the same refinery
produced the same amount of gasoline
with the same benzene content they
would earn the same amount of credits.
The standard credit generation
opportunities for overcomplying with
the standard would continue
indefinitely.
The refinery cost model discussed
further in section IX.A, predicts which
refineries would reduce benzene levels
in an order of precedence based on cost
until the 0.62 vol% refinery average
standard is achieved. The model also
predicts which refineries would
overcomply with the standard in 2011
and beyond and in turn generate
standard credits.257 Credits would be
generated by two main sources.
First, standard credits would be
generated by refineries whose current
gasoline benzene levels are already
below the 0.62 vol% standard.
According to the model, 19 refineries
are predicted to maintain current
gasoline benzene levels and overcomply
257 The refinery cost model assumes that all
credits generated are used each year. To the extent
that this does not occur, more refiners would have
to invest in technology to comply, increasing the
cost of the program.
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with the standard without making any
additional process improvements. These
refineries would generate approximately
42 million gallons of benzene credits
per year without making any investment
in technology. Additionally, the model
predicts that 5 other refineries would
reduce gasoline benzene levels even
further below 0.62 vol% resulting in
deeper overcompliance and an
additional 6 million gallons of benzene
credits per year.
Second, standard credits would be
generated by refineries whose current
gasoline benzene levels are above 0.62
vol% but are predicted by the model to
overcomply with the standard based on
existing refinery technology, access to
capital markets, and/or proximity to the
benzene chemical market. The model
predicts that 34 refineries with gasoline
benzene levels above 0.62 vol% would
make process improvements to reduce
benzene levels below the standard and
in turn generate approximately 40
million gallons of benzene credits per
year.
For the refineries which the model
predicts to make process changes to
overcomply with the standard, the
incremental cost to overcomply is
relatively small or even profitable in
some cases of benzene extraction.258 As
expected, refineries with the lowest
compliance costs would have the
greatest incentive to overcomply based
on the value of the credits to the
refining industry.
3. Credit Use
We are proposing that refiners and
importers could use benzene credits
generated or obtained under the
provisions of the ABT program to
comply with the 0.62 vol% gasoline
benzene standard in 2011 and
indefinitely thereafter. Refineries and
importers could use credits to comply
on a one-for-one basis, applying each
benzene gallon credit to offset the same
volume of benzene produced in gasoline
above the standard. For example, if in
2011 a refinery’s annual average
benzene level was 0.72, the number of
benzene credits needed to comply
would be determined based on the
margin of under-compliance with the
standard (0.72¥0.62 = 0.10 vol%)
divided by 100 and multiplied by the
258 Despite the low costs of benzene extraction,
without a benzene control standard refiners are
reluctant to invest in capital-intensive processes
such as extraction. This is because many other
projects involving capital investments that they
may be considering typically have a better or more
certain payout (past price volatility in the benzene
chemical market can discourage future investment).
Thus, refiners tend to postpone capital projects
such as extraction even if they may appear to be
profitable today.
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gallons of gasoline produced during the
2011 calendar year. The credits needed
would be expressed in gallons of
benzene.
We believe that individual refineries
would rely differently upon credits,
depending on their unique refinery
situations. As mentioned earlier, the
current range in gasoline refinery
technologies and starting benzene levels
would make it significantly more
expensive for some refineries to comply
with the standard based on actual
reduced benzene levels than others. As
such, some technologically-challenged
refiners may choose to rely largely or
entirely upon credits because it would
be much more economical than making
process improvements to reduce
benzene levels. Other refiners may
choose to make incremental process
improvements to reduce refinery
benzene levels and then rely partially
on credits to fully comply. Still others
may choose to reduce benzene levels to
at or around 0.62 vol% and maintain an
‘‘emergency supply’’ of credits to
address short-term spikes in benzene
levels due to refinery malfunctions.
Overall, the proposed credit trading
program would encourage low-cost
refineries to comply or overcomply with
the standard while allowing high-cost
refineries to rely upon credits to
comply. This would reduce the total
economic burden to the refining
industry.
a. Credit Trading Area
We are proposing a nationwide credit
trading program with no geographic
restrictions on trading. In other words,
a refiner or importer could obtain
benzene credits and use them towards
compliance regardless of where the
credits were generated. We believe that
restricting credit trading could reduce
refiners’ incentive to generate credits
and hinder trading essential to this
program. As explained in Chapter 6 of
the RIA, if PADD restrictions were
placed on credit trading, there would be
an imbalance between the supply and
demand of credits.
In other fuel standard ABT programs
(e.g., the highway diesel sulfur
program), credit trading restrictions
were necessary to ensure there was
adequate low-sulfur fuel available in
each geographic area to meet the
corresponding vehicle standard. Since
there is no vehicle emission standard
being proposed that is dependent on
gasoline benzene content, we do not
believe there is a need for geographic
trading restrictions. As mentioned
above, we project that under the
proposed ABT program, all areas of the
country (i.e., all PADDs) would
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experience a large reduction in gasoline
benzene levels as a result of the
standard.
As discussed earlier, California
gasoline would not be subject to the
proposed benzene standards. However,
California refiners that produce gasoline
that is used outside of California would
be able to generate credits on that
gasoline (and use credits to achieve
compliance on their non-California
gasoline if necessary). Likewise, as
proposed, refiners outside of California
that produce gasoline that is used in
California would not be allowed to use
that gasoline as the basis for any credit
generation, or compliance with the
proposed benzene standard. However,
we request comment on whether and
how credits could be allowed to be
generated on California gasoline
benzene reductions and applied to the
benzene compliance for non-California
gasoline.
EPA seeks comment on the proposed
nationwide trading provision, its effect
on incentives for refiners to generate
credits, and environmental impacts.
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b. Credit Life
We are proposing limited credit life to
enable proper enforcement of the
program and to encourage trading of
credits. Since the proposed standard is
a refinery gate standard (i.e., enforced as
the fuel leaves the refinery) with no
enforceable downstream standard, it is
critical that EPA be able to conduct
enforcement at the refinery. A
reasonable limitation on credit life
would allow EPA to verify the validity
of credits through record retention.
Credit information must be
independently verifiable such that, in
the event of violations involving credits,
the liable party is identifiable and
accountable. EPA enforcement activities
are limited by the five-year statute of
limitations in the Clean Air Act. As a
consequence, credit life greater than five
years creates potentially serious
enforcement difficulties. This is
particularly important given the ongoing
changes in business relationships,
ownership, and merger practices that
are characteristic of the refining
industry. In addition, since credit
trading plays an essential role in
moderating program costs, it is
important that refiners have an
incentive to trade credits rather than
hoard them. Instituting a credit
expiration date would promote trading
because refiners would be forced to ‘‘use
it or lose it.’’ In summary, we believe
the proposed credit life provisions,
described in more detail below, are
limited enough to satisfy enforcement
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and trading concerns yet sufficiently
long to provide program flexibility.
We are proposing that standard
credits generated in 2011 and beyond
would have to be used within five years
of the year in which they were
generated. For example, credits
generated based on 2011 gasoline
production would have to be used
towards compliance with the 2016
calendar year or earlier, otherwise they
would expire. Standard credits traded to
another party would still have to be
used during the same five-year period
because credit life is tied to the date of
generation, not the date of transfer.
We are proposing that early credits
generated prior to 2011 (discussed in
the paragraphs to follow) would have a
three-year credit life from the start of the
program. In other words, early credits
would have to be applied to the 2011,
2012, and/or 2013 compliance years or
they would expire.
These proposed credit life provisions
are similar to those finalized in the
gasoline sulfur program, except the
early credit life is three years instead of
two. We are proposing a three-year early
credit life because it corresponds with
the number of early credits projected to
be generated according to our refinery
cost model.259 Additionally, we predict
that three years would be more than
sufficient time for all early credits
generated to be utilized. We believe that
this certainty that all credits could be
utilized would strengthen refiners’
incentive to generate early credits and
subsequently establish a more reliable
credit market for trading.
In addition to the above-mentioned
provisions, we are proposing that credit
life may be extended by two years for
early credits and/or standard credits
generated by or traded to approved
small refiners. We are offering this
provision as a mechanism to encourage
more credit trading to small refiners.
Small refiners often face special
technological challenges, so they would
tend to have more of a need to rely on
credits. At the same time, they often
have fewer business affiliations than
other refiners, so they could have
difficulty obtaining credits. We believe
this provision would be equally
beneficial to refiners generating credits.
This additional credit life for credits
traded to small refiners would give
refiners generating credits a greater
opportunity to fully utilize the credits
before they expire. For example, a
refiner who was holding on to credits
for emergency purposes or other reasons
later found to be unnecessary, could
259 Derivation of three-year early credit lag is
found in Chapter 6 of the RIA (section 6.5.3.1).
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trade these credits at the end of their life
to small refiners who could utilize them
for two more years. However, EPA is
concerned that extending credit life
beyond the five-year statute of
limitations in the Clean Air Act (net 7year credit life for standard credits
generated by or traded to small refiners)
could create significant enforceability
problems. Consequently, EPA seeks
comment on provisions that could be
included in the regulations that would
address this enforceability concern
regarding the extended credit life for
small refiner standard credits.
As discussed in Section X.A, we are
also seeking comment on different ways
of structuring the program that may be
able to allow for unlimited credit life
since, unlike in the gasoline sulfur
program, there is no vehicle standard
being proposed that is dependent on
fuel quality. We considered that
unlimited credit life could further
promote credit generation and allow
refiners to maintain an ongoing supply
of credits in the event of an emergency.
However, for several reasons we have
elected to propose a limited credit life
based on the context of the rest of the
proposed program. If unlimited credit
life were to discourage trading of
credits, this could force refineries with
more expensive benzene control
technologies to comply and thus
increase the total cost of the program. In
addition, unlimited credit life would
make it more difficult to verify
compliance with the standard. One way
of addressing this concern would be to
require refiners to retain credit records
indefinitely. Even then, given the fluid
nature of refiner and importer
ownership in recent years, in many
cases it would still be difficult to verify
the validity of historical credit
generation and use. Since the proposed
benzene standard would be enforced
solely at the refinery, it is critical that
such enforcement be as simple and
straightforward as possible.
Nonetheless, as discussed in Section
X.A, it may be possible to design the
overall program in such a way to
address these concerns and still allow
for infinite credit life.
In conclusion, we are proposing a
reasonably limited credit life for both
early and standard benzene credits. We
seek comment on unlimited credit life.
Please share with us any additional
ideas you may have on how unlimited
credit life could be beneficial to this
program and/or how associated
recordkeeping and enforcement issues
could be mitigated.
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4. Early Credit Generation (2007–2010)
To encourage early application of and
innovation in benzene control
technology, we are proposing that
refiners could generate early benzene
credits from June 1, 2007 to December
31, 2010 by making qualifying
reductions from their pre-determined
refinery baselines. A discussion of how
refinery baselines are established and
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The credits generated under the early
credit program could be used to provide
refiners with additional lead time to
make their investments. If properly
implemented, we project that the delay
could be as much as three years as
described in Chapter 6 of the RIA.
Accordingly, we are proposing a threeyear early credit life, as discussed
earlier. The additional lead time would
allow the refining industry to spread out
demand for design, engineering,
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what constitutes a qualifying benzene
reduction is found in the subsections to
follow. The early credits generated
under this program would be
interchangeable with the standard
credits generated in 2011 and beyond
and would follow the above-mentioned
credit use provisions.
The early reductions we are projecting
to occur would be the initial steps of
each refinery’s ultimate benzene control
strategy, but completed earlier than
required. We project that from mid-2007
to 2010, refiners could implement
operational changes and/or make small
capital investments to reduce gasoline
benzene. These actions would create a
two-step phase down in gasoline
benzene prior to 2011 as shown in
Figure VII.D–1.
construction and other related services,
reducing overall compliance costs.
Importers would not be permitted to
generate early credits, for several
reasons.260 First, unlike refineries,
importers would not need additional
lead time to comply with the standard,
since they would not be investing in
benzene control technology.
Additionally, because importer
operations are more variable than
refinery operations, importers could
potentially redistribute the importation
of foreign gasoline based on benzene
level to generate early credits without
making a net reduction in gasoline
benzene. This type of scheme could
result in a large number of early credits
being generated with no net benzene
emission reduction value. This is not
expected to occur for refineries because
they are already operating at high
capacity and do not have the flexibility
260 As discussed in section VII.I.1 below, foreign
refiners may generate early credits under the
proposed 40 CFR 80.1420 provisions.
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to quickly increase, decrease, or shift
production volumes. Additionally,
under the proposed program, refineries
are prohibited from moving benzenerich blendstocks around to generate
early credits as described below.
We believe that refiners would have
several motivations for making early
benzene reductions. For refiners who
have a series of technology
improvements to make, early innovative
improvements would help the refiner
get one step closer to compliance. Early
reductions would also generate credits
which could be used to postpone
subsequent investments. For refiners
capable of making early advancements
to reduce their benzene levels below
0.62 vol%, the early credits generated
would not be needed for their own
future use. For these refiners, trading
early credits to other refiners may be a
way to offset the cost of their early
capital investment(s).
a. Establishing Early Credit Baselines
We are proposing that any refiner
planning on generating early credits
would have to obtain an individual
refinery benzene baseline in order to
provide a starting point for calculating
early credits.
Refinery benzene baselines would be
defined as the annualized volumeweighted benzene content of gasoline
produced at a refinery from January 1,
2004 to December 31, 2005. We are
proposing a two-year baseline period to
account for normal operational
fluctuations in benzene level. We
propose using the 2004 and 2005
calendar years because we believe this
would represent the most current batch
gasoline data available prior to today’s
proposal.
We would require refiners to submit
individual baselines for each refinery
that is planning to generate early
benzene credits. Refinery benzene
baselines would be calculated using the
2004–2005 batch data submitted to us
under the RFG and Anti-dumping
requirements.261 We propose that joint
ventures, in which two or more refiners
collectively own and operate one or
more refineries, be treated as separate
refining entities for early credit
generation purposes.
Refiners would be required to submit
their refinery baselines in writing to
EPA. We propose that refiners could
begin applying for 2004–05 benzene
baselines as early as March 1, 2007.
There would be no single cut-off date
for applying for a baseline; however, a
refiner planning on generating early
261 RFG, 40 CFR 80.75; Anti-dumping, 40 CFR
80.105.
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credits would need to submit a baseline
application at least 60 days prior to
beginning credit generation. We are
proposing a shorter notification period
for this rule (past rules were 120 days)
to accommodate our proposed early
credit generation start date of June 1,
2007. EPA would review all baseline
applications and notify the refiner of
any discrepancies found with the data
submitted. If we did not respond within
60 days, the baseline would be
considered to be approved, subject to
later review by EPA.
Under the proposed program, refiners
would be prohibited from moving
gasoline and gasoline blendstock
streams from one refinery to another in
order to generate early credits. This type
of transaction would result in artificial
credits with no associated emission
reduction value. If traded and used
towards compliance, these artificial
credits could negatively impact the
benefits of the program. We considered
basing credit generation for multirefinery refiners on corporate benzene
baselines instead of individual refinery
baselines, but determined that this
could hinder credit generation. If a valid
reduction was made at one refinery and
an unrelated expansion occurred at
another facility during this time, the
credits earned based on a corporate
baseline could be reduced to zero.
Instead, we propose to validate early
credits based on existing reporting
requirements (e.g., batch reports and
pre-compliance reporting data). We seek
comment on this approach.
b. Early Credit Reduction Criteria
(Trigger Points)
We are proposing that to generate
early credits, refiners would first need
to reduce gasoline benzene levels to
0.90 times their refinery benzene
baseline during a given averaging
period. The purpose of setting an early
credit generation trigger point is to
ensure that changes in benzene level are
representative of real process
improvements. Without a trigger point,
refineries could generate ‘‘windfall’’
early credits based on normal year to
year fluctuations in benzene level
associated with MSAT1. These artificial
credits would compromise the
environmental benefits of an ABT
program because they would have no
real associated benzene emission
reduction value.
In designing the early credit
generation program, we considered a
variety of different types of trigger
points. We performed sensitivity
analyses around absolute level trigger
points (refineries must reduce gasoline
benzene levels to a certain
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concentration), fixed reduction trigger
points (refineries must reduce gasoline
benzene levels by a certain
concentration), and percent reduction
trigger points (refineries must reduce
gasoline benzene by a percentage).
Based on our analysis found in Chapter
6 of the RIA, we found absolute level
trigger points to be too restrictive for
high benzene level refineries that could
benefit from reductions the most. We
also found fixed reduction trigger points
to be too restrictive to low benzene level
refineries which would be penalized for
already being ‘‘cleaner.’’ Percent
reduction trigger points were found to
be consistently limiting towards all
refineries, regardless of starting benzene
level. As such, we propose to conclude
that a percent reduction trigger point
would be the most appropriate early
credit validation tool to address the
wide range in starting benzene levels.
To determine an appropriate value for
the percent reduction trigger point, we
considered a range of reductions from
5–40% and examined the resulting early
credit generation outcomes. We found
that as the value of the percent
reduction trigger point increased, the
potential for windfall credit generation
decreased, but unfortunately so did the
number of early credits generated from
legitimate refinery modifications. To
address this competing relationship
between windfall and early credit
generation, we are proposing a 10%
reduction trigger point. We believe that
this trigger point is restrictive enough to
prevent most windfall credit generation,
but not too restrictive to discourage
refineries from making early benzene
reductions. The proposed 10%
reduction trigger point roughly
coincides with the average fluctuation
in benzene level in 2004 as discussed in
Chapter 6 of the RIA. A 10% reduction
trigger point for early credits was also
finalized in the gasoline sulfur
rulemaking, which also affected the
entire gasoline pool and had to
encompass a variety of unique refinery
situations.262 EPA requests comments
on the proposed trigger point and seeks
alternate recommendations for
validating early credits.
c. Calculating Early Credits
We are proposing that once the 10%
reduction trigger point was met,
refineries could generate early credits
based on the entire reduction. In terms
of benzene levels, a refinery would first
have to reduce its average benzene level
to 0.90 times its original baseline
benzene level during a given averaging
period in order to generate credits. For
262 40
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example, if in 2008 a refinery reduced
its annual benzene level from a baseline
of 2.00 vol% to 1.50 vol% (below the
trigger of 0.90 × 2.00 = 1.80 vol%), its
benzene credits would be determined
based on the difference in annual
benzene content (2.00¥1.50 = 0.50
vol%) divided by 100 and multiplied by
the gallons of gasoline produced in
2008. The credits would be expressed in
gallons of benzene.
5. Additional Credit Provisions
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a. Credit Trading
The potential exists for credits to be
generated by one party, subsequently
transferred or used in good faith by
another, and later found to have been
calculated or created improperly or
otherwise determined to be invalid. As
in past programs, we propose that
should this occur both the seller and
purchaser would have to adjust their
benzene calculations to reflect the
proper credits and either party (or both)
could be determined to be in violation
of the standards and other requirements
if the adjusted calculations demonstrate
noncompliance with the 0.62 vol%
standard. This would allow the credit
market to properly allocate any such
risk.
As with ABT programs in other rules,
we are proposing that credits should be
transferred directly from the refiner or
importer that generated them to the
party that would use them for
compliance purposes. This would
ensure that the parties purchasing them
would be better able to assess the
likelihood that the credits were valid,
and would aid in compliance
monitoring. An exception would exist
where a credit generator transferred
credits to a refiner or importer who
could not use all the credits, in which
event that transferee could transfer the
credits to another refiner or importer.
However, based on the increased
difficulty in assuring the validity of
credits as the credits change hands more
than once, we are proposing that credits
could only be transferred a limited
number of times. We are requesting
comment on the maximum number of
allowable trades, in the range of 2 to 4
trades. After the maximum number of
trades, such credits would have be used
or terminated.
We propose no prohibitions against
brokers facilitating the transfer of credits
from one party to another. Any person
could act as a credit broker, whether or
not such person was a refiner or
importer, so long as the title to the
credits was transferred directly from the
generator to the user. Further discussion
of these credit trading provisions and
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alternative options is found in section
X.A below.
necessary to prevent the development of
major problems.
b. Pre-Compliance Reporting
Requirements
In order to provide an early indication
of the credit market for refiners
planning on relying upon benzene
credits as a compliance strategy in 2011
and beyond, we are requesting that
refiners submit pre-compliance reports
to us in 2008, 2009, and 2010. EPA
would then summarize this information
(in such a way as to protect confidential
business information) in a report
available to the industry. This is similar
to the way pre-compliance reports are
used for the ultra-low sulfur diesel
program. In addition, we are proposing
that refiners provide us with a final
summary pre-compliance report in
2011, to allow for a complete account of
early credit generation.263 The reports
would be due annually by June 1st and
would contain refiners’ most up-to-date
implementation plans for complying
with the 0.62 vol% benzene standard.
More specifically, we would require
refiners to annually submit to us
engineering and construction plans and
the following data:
—Actual/projected gasoline production
volume and average benzene level for
the June 1, 2007 through December
31, 2007 annual averaging period, and
for the 2008–2015 annual averaging
periods.
—Actual/projected early credits
generated during the June 1, 2007
through December 31, 2007 annual
averaging period, and for the 2008–
2010 annual averaging periods (June 1
through December 31, 2007 and 2008–
2014 for small refiners).
—Standard credits projected to be
generated during the 2011–2015
annual averaging periods (2015 for
small refiners).
—Credits projected to be needed for
compliance during 2011–2015 annual
averaging periods (2015 for small
refiners).
6. Special ABT Provisions for Small
Refiners
Pre-compliance reporting has proven
to be an indispensable mechanism in
implementing the gasoline and diesel
sulfur programs, and we expect this to
be the case in today’s proposed
program. A detailed understanding of
how individual refiners and the
industry at large are progressing toward
final implementation of the proposed
standards would help identify early
concerns and allow timely action if
263 Based on their proposed January 1, 2015
compliance date, small refiners would be required
to submit annual pre-compliance reports to us in
2008 through 2014 with a final summary precompliance report in 2015.
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Approved small refiners would follow
all the above-mentioned ABT provisions
with the exception of special credit
generation provisions which
accommodate their 2015 compliance
start date. Early credits could be
generated by small refiners from June 1,
2007 to December 31, 2014 for refineries
that reduce their average gasoline
benzene level to 0.90 times their
original 2004–2005 baseline level.
Standard credits could also be generated
by small refiners beginning January 1,
2015 and continuing indefinitely for
refineries that overcomply with the
standard by producing gasoline with an
annual average benzene content below
0.62 vol%. Additionally, all credits
generated by or traded to approved
small refiners would have an additional
two-year credit life as described above
in VII.D.3.b.
E. Regulatory Flexibility Provisions for
Qualifying Refiners
1. Hardship Provisions for Qualifying
Small Refiners
In developing our proposed MSAT
program, we evaluated the need and the
ability of refiners to meet the proposed
benzene standards as expeditiously as
possible. We believe it is feasible and
necessary for the vast majority of the
program to be implemented in the
proposed time frame to achieve the air
quality benefits as soon as possible.
However, based on information
available from small refiners, we believe
that refineries owned by small
businesses generally face unique
hardship circumstances, compared to
larger refiners. Thus, we are proposing
several special provisions for refiners
that qualify as ‘‘small refiners’’ to
reduce the disproportionate burden that
the proposed standards would have on
these refiners. These provisions are
discussed in detail below.
a. Qualifying Small Refiners
EPA is proposing several special
provisions that would be available to
companies that are approved as small
refiners. Small refiners generally lack
the resources available to larger
companies that help large companies,
including those large companies that
own small-capacity refineries, to raise
capital for investing in benzene control
equipment. These resources include
shifting internal funds, securing
financing, or selling assets. Small
refiners are also likely to have more
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difficulty in competing for engineering
resources and completing construction
of the needed benzene control
equipment (and any necessary octane
recovery) equipment in time to meet the
standards proposed today. Therefore,
we are proposing small refiner relief
provisions in today’s action as an aspect
of realizing the greatest emission
reductions achievable.
Since small refiners are more likely to
face hardship circumstances than larger
refiners, we are proposing temporary
provisions that would provide
additional time to meet the benzene
standards for refineries owned by small
businesses. This approach would allow
the overall program to begin as early as
possible, while still addressing the
ability of small refiners to comply.
i. Regulatory Flexibility for Small
Refiners
As explained in the discussion of our
compliance with the Regulatory
Flexibility Act below in section XII.C
and in the Initial Regulatory Flexibility
Analysis in Chapter 14 of the RIA, we
considered the impacts of today’s
proposed regulations on small
businesses. Most of our analysis of small
business impacts was performed as a
part of the work of the Small Business
Advocacy Review (SBAR) Panel
convened by EPA, pursuant to the
Regulatory Flexibility Act as amended
by the Small Business Regulatory
Enforcement Fairness Act of 1996
(SBREFA). The final report of the Panel
is available in the docket for this
proposed rule.
For the SBREFA process, EPA
conducted outreach, fact-finding, and
analysis of the potential impacts of our
regulations on small businesses. Based
on these discussions and analyses by all
Panel members, the Panel concluded
that small refiners in general would
likely experience a significant and
disproportionate financial hardship in
reaching the objectives of today’s
proposed program.
One indication of this
disproportionate hardship for small
refiners is the higher per-gallon capital
costs projected for the removal of
benzene from gasoline under the
proposed program. Refinery modeling of
refineries owned by refiners likely to
qualify as small refiners, and of nonsmall refineries, indicates that small
refiners could have significantly higher
costs to apply some technologies. For
two of the technologies that we believe
that refiners would use to reduce their
benzene levels, routing the six carbon
hydrocarbon compounds around the
reformer and isomerizing these
compounds, we anticipate that small
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refiners’ costs would likely be similar to
non-small refiners, as very little capital
investment would need to be made for
these technologies. However, for
technologies such as benzene saturation
and benzene extraction, we anticipate
that the costs to small refiners would be
higher. Due to the poorer economies of
scale, benzene saturation is expected to
cost small refiners about 2.2 cents per
gallon (while it is projected that
benzene saturation would cost a nonsmall refinery about 1.3 cents per
gallon).264 Likewise, benzene extraction
is estimated to cost those refineries able
to use this technology about 0.1 cents
per gallon; however, for small refiners
benzene extraction is expected to cost
about 0.5 cents per gallon.
The Panel also noted that the burden
imposed on the small refiners by the
proposed benzene standard could vary
from refiner to refiner. Thus, the Panel
recommended that more than one type
of burden reduction be offered so that
most, if not all, small refiners could
benefit. We have continued to consider
the issues that were raised during the
SBREFA process and have decided to
propose the provisions recommended
by the Panel.
ii. Rationale for Small Refiner
Provisions
Generally, we structured these
proposed provisions to reduce the
burden on small refiners while still
achieving the air quality benefits that
this program would provide. We believe
that the proposed regulatory flexibility
provisions for small refiners are a
necessary aspect of standards reflecting
the greatest achievable emission
reductions considering costs and lead
time, because they would appropriately
adjust potential costs and lead time for
the dissimilarly situated small refiner
industry segment, and at the same time
allow EPA to propose a uniform
benzene standard for all refineries.
First, the proposed compliance
schedule for this program, combined
with flexibility for small refiners, would
achieve the air quality benefits of the
program as soon as possible, while still
ensuring that small refiners that choose
to comply by raising capital for benzene
reduction technologies would have
adequate time to do so. As noted above,
most small refiners have limited
264 Smaller refineries are less likely to be able to
take advantage of economies of scale. For example,
a portion of the capital costs invested for a benzene
control unit is fixed (i.e., engineering design costs)
resulting in similar costs for each investment
project. However, when amortized over the volume
of fuel processed by a small versus large unit, the
per-gallon capital costs are higher for the smaller
unit, resulting in poorer economies of scale.
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additional sources of income or capital
beyond refinery earnings for financing
and typically do not have the financial
backing that larger and generally more
integrated companies have. Therefore,
they could benefit from additional time
to accumulate capital internally or to
secure capital financing from lenders.
Second, providing small refiners more
time to comply would increase the
availability of engineering and
construction resources to them. Some
refiners would need to install additional
processing equipment to meet the
proposed benzene standard. We
anticipate that there could be increased
competition for technology services,
engineering resources, and construction
management and labor. In addition,
vendors would be more likely to
contract with the larger refiners first, as
their projects would offer larger profits
for the vendors. Temporarily delaying
compliance for small refiners would
spread out the demand for these
resources and probably reduce any cost
premiums caused by limited supply.
Third, we are anticipating that many
small refiners may choose to comply
with the proposed benzene standard by
purchasing credits. Having additional
lead time (which could also result in
additional time to generate credits for
some small refiners) could help to
ensure that there would be sufficient
credits available and that there would
be a robust credit trading market.
Furthermore, offering two years of
additional credit life for credits traded
to small refiners, as discussed in section
VII.D.3.b, would improve credit
availability.
Lastly, we recognize that while the
proposed benzene standard may be
achieved using the four technologies
suggested above, new technologies may
also be developed that may reduce the
capital and/or operational costs. Thus,
we believe that allowing small refiners
some additional time for newer
technologies to be proven out by other
refiners would have the added benefit of
reducing the risks faced by small
refiners. The added time would likely
allow for small refiners to benefit from
the lower costs of these technologies.
This would help to offset the potentially
disproportionate financial burden facing
small refiners.
We discuss below the provisions that
we are proposing to help mitigate the
effects on small refiners. Small refiners
that chose to make use of the small
refiner delayed provision would also
delay, to some extent, the benzene
emission reductions that would
otherwise have been achieved.
However, the overall impact of these
postponed reductions would be
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reasonable, for several reasons. Small
refiners represent a relatively small
fraction of national gasoline production.
Our current estimates (of refiners that
we expect would qualify as small
refiners) indicate that these refiners
produce about 2.5 percent of the total
gasoline pool. In addition, these small
refiners are generally dispersed
geographically across the country and
the gasoline that they produce is
sometimes transported to other areas, so
the limited loss in benzene emissions
reduction would also be dispersed.
Finally, absent small refiner flexibility,
EPA would likely have to consider
setting a less stringent benzene standard
or delaying the overall program (until
the burden of the program on many
small refiners was diminished), which
would serve to reduce and delay the air
quality benefits of the overall program.
By providing temporary relief to small
refiners, we are able to adopt a program
that would reduce benzene emissions in
a timely and feasible manner for the
industry as a whole.
The proposed small refiner provisions
should be viewed as a subset of the
hardship provisions described in
section VII.E.2.b. Rather than dealing
with many refineries on a case-by-case
basis through the general hardship
provisions (described later), we limit the
number by proposing to provide
predetermined types of relief to a subset
of refineries based on criteria designed
to identify refineries most likely to be in
need of such automatic relief.
b. How Do We Propose To Define Small
Refiners for the Purpose of the Hardship
Provisions?
The definition of small refiner for this
proposed program is in most ways the
same as our small refiner definitions in
the Gasoline Sulfur and Highway and
Nonroad Diesel rules. These definitions,
in turn, were based on the criteria use
by the Small Business Administration.
However, we are proposing to clarify
some ambiguities about the definition
that have existed in the past.
A small refiner would need to
demonstrate that it met all of the
following criteria:
Produced gasoline from crude during
calendar year 2005.
Small refiner provisions would be
limited to refiners of gasoline from
crude because they would be the ones
that bore the investment burden and
therefore the inherent economic
hardship. Therefore, blenders and
importers would not be eligible, nor
would be additive component
producers.
Small refiner status would be limited
to refiners that owned and operated the
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refinery during the period from January
1, 2005 through December 31, 2005.
New owners that purchased a refinery
after that date would do so with full
knowledge of the proposed regulations,
and should have planned to comply
along with their purchase decisions. As
with the earlier fuel rules, we are
proposing that a refiner that restarts a
refinery in the future may be eligible for
small refiner status. Thus, a refiner
restarting a refinery that was shut down
or non-operational between January 1,
2005 and January 1, 2006 could apply
for small refiner status. In such cases,
we would judge eligibility under the
employment and crude oil capacity
criteria based on the most recent 12
consecutive months prior to the
application, unless we conclude from
data provided by the refiner that another
period of time is more appropriate.
However, unlike past fuel rules, we
propose to limit this to a company that
owned the refinery at the time that it
was shut down. New purchasers would
not be eligible for small refiner status for
the same reasons described above.
Companies with refineries built after
January 1, 2005 would also not be
eligible for the small refiner hardship
provisions.
—Had no more than 1,500 employees,
based on the average number of
employees for all pay periods from
January 1, 2005 to January 1, 2006;
and,
—Had a crude oil capacity less than or
equal to 155,000 barrels per calendar
day (bpcd) for 2005.
In determining its total number of
employees and crude oil capacity, a
refiner would need to include the
number of employees and crude oil
capacity of any subsidiary companies,
any parent companies, any subsidiaries
of the parent companies, and any joint
venture partners. There has been some
confusion in past rules regarding how
these provisions were interpreted, and
as a result, we are proposing to clarify
(and, in some cases, modify) them here.
For example, in previous rules we
defined a subsidiary to be a company in
which the refiner or its parent(s) has a
50 percent or greater interest. We realize
that it is possible for a parent to have
controlling ownership interest in a
subsidiary despite having less than 50
percent ownership. Similarly, we realize
that it is also possible for multiple
parents to each have less than 50
percent ownership interest but still
maintain a controlling ownership
interest. Therefore, in order to clarify
our rules, we are proposing to define a
parent company as any company (or
companies) with controlling interest,
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and to define a subsidiary of a company
to mean any company in which the
refiner or its parent(s) has a controlling
ownership interest. In many cases, there
are likely to be multiple layers of parent
companies, with the ultimate parent
being the one for which no one else has
controlling interest. The employees and
crude capacity of all parent companies,
and all subsidiaries of all parent
companies, would thus be taken into
consideration when evaluating
compliance with these criteria.
As with our earlier fuel sulfur
regulations, we are also proposing today
that refiners owned and controlled by
an Alaska Regional or Village
Corporation organized under the Alaska
Native Claims Settlement Act, would
also be eligible for small refiner status,
based only on the refiner’s employees
and crude oil capacity.265
c. What Options Would Be Available
For Small Refiners?
We are proposing several provisions
today to help reduce the burdens on
small refiners, as discussed above. In
addition, these provisions would also
allow for incentives for small refiners
that make reductions to their benzene
levels.
i. Delay in Standards
We propose that small refiners be
allowed to postpone compliance with
the proposed benzene standard until
January 1, 2015, which is four years
after the general program would begin.
While all refiners would be allowed
some lead time before the general
proposed program began, we believe
that in general small refiners would still
face disproportionate challenges. The
proposed four-year delay for small
refiners would help mitigate these
challenges. Further, previous EPA fuel
programs have included two to four year
delays in the start date of the effective
standards for small refiners, consistent
with the lead time we believe
appropriate here.
Small refiners have indicated to us
that an extension of available lead time
would allow them to more efficiently
carry out necessary capital projects with
less direct competition with non-small
refiners for financing and for contractor
to carry out capital improvements.
There appears to be merit in this
position, and we propose that approved
small refiners have four years of
additional lead time. This would
provide three years after the 2012
review of the program, which we
believe would be enough time for such
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refiners to complete necessary capital
projects if they chose to pursue them.
ii. ABT Credit Generation Opportunities
While we have anticipated that many
small refiners would likely find it more
economical to purchase credits for
compliance, some have indicated they
would make reductions to their gasoline
benzene levels to meet the proposed
benzene standard. Further, a few small
refiners indicated that they would likely
do so earlier than would be required by
the January 1, 2015 proposed small
refiner start date. Therefore, we are
proposing that early credit generation be
allowed for small refiners that take steps
to meet the benzene requirement prior
to their effective date. Small refiner
credit generation would be governed by
the same rules as the general program,
described above in section VII.D, the
only difference being that small refiners
would have an extended early credit
generation period of up to seven years.
Early credits could be generated by
small refiners making qualifying
reductions from June 1, 2007 to
December 31, 2014, after which credits
could be generated indefinitely for those
that overcomplied with the standard.
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iii. Extended Credit Life
As discussed previously, in order to
encourage the trading of credits to small
refiners, we are proposing that the
useful life of credits be extended by 2
years if they are generated by or traded
to small refiners. This is meant to
directly address concerns expressed by
small refiners that they would be unable
to rely on the credit market to avoid
large capital costs for benzene control.
iv. ABT Program Review
As previously stated, we are
anticipating that it may be more
economically sound for some refiners to
purchase and use credits. During
discussions with small refiners, all of
the small refiners voiced their concerns
about reliance on a credit market for
compliance with the benzene standard.
Specifically, small refiners feared that:
(1) there could be a shortage of credits,
(2) that larger refiners would not trade
credits with smaller refiners, and (3)
that the cost of credits could be so high
that the option to purchase credits for
compliance would not be a viable
option. Due to these concerns it was
suggested that EPA perform a review of
the ABT program (and thus, the small
refiner flexibility options) by 2012, one
year after the general program begins.
Such a review would take into
account the number of early credits
generated, as well as the number of
credits generated and transferred during
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the first year of the overall benzene
control program. Further, requiring the
submission of pre-compliance reports
from all refiners, similar to the highway
and nonroad diesel programs, would aid
in assessing the ABT program prior to
performing the review. A small refiner
delay option of four years after the
compliance date for other refiners,
coupled with a review after the first year
of the overall program, would still
provide small refiners with roughly
three years that we believe would be
needed to obtain financing and perform
engineering and construction. We are
proposing to perform a review within
the first year of the overall program (i.e.,
by 2012). To aid the review, we are also
proposing the requirement that all
refiners submit refinery pre-compliance
reports annually beginning June 1, 2008.
Refiners’ 2011 annual compliance
reports will be similar to the precompliance reports, but the annual
compliance reports will also contain
information such as credits generated,
credits used, credits banked, credit
balance, cost of credits purchased. EPA
would aggregate the data (to protect
individual refiners’ confidentiality) and
make the results available to the
industry. When combined with the fouryear delay option, this would provide
small refiners (and others) with the
knowledge of the credit trading market’s
status before they would need to make
a decision to either purchase credits or
to obtain financing to invest in capital
equipment.
Further, we are requesting comment
on elements to be included in the ABT
program review, and suggested actions
that could be taken following such a
review. Such elements could include:
—Revisiting the small refiner provisions
if it is found that the credit trading
market did not exist to a sufficient
degree to allow them to purchase
credits, or that credits were only
available at a cost-prohibitive price.
—Options to either help the credit
market, or help small refiners gain
access to credits.
With respect to the first element, the
SBAR Panel recommended that EPA
consider establishing an additional
hardship provision to assist any small
refiners that were unable to comply
with the benzene standard even with a
viable credit market. Such a hardship
provision would address the case of a
small refiner for which compliance
would be feasible only through the
purchase of credits, but it was not
economically feasible for the refiner to
do so. This hardship would be provided
to a small refiner on a case-by-case basis
following the review and based on a
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summary, by the refiner, of technical or
financial infeasibility (or some other
type of similar situation that would
render its compliance with the standard
difficult). This hardship provision might
include further delays and/or a slightly
relaxed standard on an individual
refinery basis for up to two years.
Following the two-year relief, a small
refiner would be allowed to request
multiple extensions of the hardship
until the refinery’s material situation
changed. We are proposing the
inclusion of such a hardship provision
which could be applied for following,
and based on the results of, the ABT
program review.
With respect to the second element,
the Panel recommended that EPA
develop options to help the credit
market if it is found (following the
review) that there is not an ample
supply of credits or that small refiners
are having difficulty obtaining credits.
These options could include the
‘‘creation’’ of credits by EPA that would
be introduced into the credit market to
ensure that there are additional credits
available for small refiners. Another
option the Panel discussed to assist the
credit market was to impose additional
requirements to encourage trading with
small refiners. These could include a
requirement that a percentage of all
credits sold be set aside and only made
available for small refiners. Similarly,
we could require that credits sold, or a
certain percentage of credits sold, be
made available to small refiners before
they are allowed to be sold to any other
refiners. Options such as these would
help to ensure that small refiners were
able to purchase credits. One such
recommendation by the Panel, to extend
credit life for small refiners, is included
in today’s proposal and described
above.
We welcome comment on additional
measures that could be taken following
the review if it was found that there was
a shortage of credits or that credits were
not available to small refiners.
d. How Would Refiners Apply for Small
Refiner Status?
A refiner applying for status as a
small refiner would be required to apply
and provide EPA with several types of
information by December 31, 2007. (The
detailed application requirements are
summarized below.) All refiners seeking
small refiner status under this program
would need to apply for small refiner
status, regardless of whether or not the
refiner had been approved for small
refiner status under another fuel
program. As with applications for relief
under other rules, applications for small
refiner status under this proposed rule
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that were later found to contain false or
inaccurate information would be void
ab initio.
Requirements for small refiner status
applications:
—The total crude oil capacity as
reported to the Energy Information
Administration (EIA) of the U.S.
Department of Energy (DOE) for the
most recent 12 months of operation.
This would include the capacity of all
refineries controlled by a refiner and
by all subsidiaries and parent
companies and their subsidiaries. We
would presume that the information
submitted to EIA is correct. (In cases
where a company disagreed with this
information, the company could
petition EPA with appropriate data to
correct the record when the company
submitted its application for small
refiner status. EPA could accept such
alternate data at its discretion.)
—The name and address of each
location where employees worked
during the 12 months preceding
January 1, 2006; and the average
number of employees at each location
during this time period. This would
include the employees of the refiner
and all subsidiaries and parent
companies and their subsidiaries.
—In the case of a refiner who
reactivated a refinery that was
shutdown or non-operational between
January 1, 2005, and January 1, 2006,
the name and address of each location
where employees worked since the
refiner reactivated the refinery and
the average number of employees at
each location for each calendar year
since the refiner reactivated the
refinery.
—The type of business activities carried
out at each location.
—An indication of the small refiner
option(s) the refiner intends to use
(for each refinery).
—Contact information for a corporate
contact person, including: name,
mailing address, phone and fax
numbers, e-mail address.
—A letter signed by the president, chief
operating officer, or chief executive
officer of the company (or a designee)
stating that the information contained
in the application was true to the best
of his/her knowledge and that the
company owned the refinery as of
January 1, 2007.
e. The Effect of Financial and Other
Transactions on Small Refiner Status
and Small Refiner Relief Provisions
In situations where a small refiner
loses its small refiner status due to
merger with a non-small refiner,
acquisition of another refiner, or
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acquisition by another refiner, we are
proposing provisions which are similar
to those finalized in the nonroad diesel
final rule to allow for an additional 30
months of lead time. A complete
discussion of this provision is located in
the preamble to the final nonroad diesel
rule.
2. General Hardship Provisions
Unlike previous fuel programs,
today’s program includes inherent
flexibility because there is a nationwide
credit trading program. Refiners would
have the ability to avoid or minimize
capital investments indefinitely by
purchasing credits, and we expect that
many refiners would utilize this option.
We also expect that refiners and
importers who normally would produce
or import gasoline that met the
proposed standard would periodically
rely on credits in order to achieve
compliance. As discussed in section
VII.D, we expect that sufficient credits
would be available on an annual basis
to accommodate the needs of the
regulated industry, and we expect that
these credits would be available at
prices that are comparable to the
alternative cost of making the capital
investment necessary to produce
compliant gasoline. We are proposing to
require that refiners submit precompliance reports beginning in 2008.
These reports would indicate how the
refinery plans to achieve compliance
with the 0.62 vol% standard as well as
the amount of credits expected to be
generated or expected to be needed. The
information provided in these reports
would enable an assessment of the
robustness of the credit market and the
ability of refiners to rely on credits as
the program began.
Although we expect credits to be
available at competitive prices to those
who need them, we are proposing
hardship provisions to accommodate an
inability to comply with the proposed
standard at the start of the program, and
to deal with unforeseen circumstances.
These provisions would be available to
all refiners, small and non-small, though
relief would be granted on a case-bycase basis following a showing of
certain requirements, primarily that
compliance through the use of credits
was not feasible. We are proposing that
any hardship waiver would not be a
total waiver of compliance. Rather, such
a waiver would allow the refiner to have
an extended period of deficit carryover.
Under regular circumstances, our
proposed deficit carryover provision
would allow an entity to be in deficit
with the proposed benzene standard for
one year, provided that they made up
the deficit and were in compliance the
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next year. The proposed hardship
provisions would allow a deficit to be
carried over for an extended, but
limited, time period. EPA would
determine an appropriate extended
deficit carryover time period based on
the nature and degree of the hardship,
as presented by the refiner in their
hardship application, and on our
assessment of the credit market. Note
that any waivers granted under this
proposed rule would be separate and
apart from EPA’s authority under the
Energy Policy Act to issue temporary
waivers for extreme and unusual supply
circumstances, under section 211(c)(4).
a. Temporary Waivers Based on
Unforeseen Circumstances
We are proposing a provision which,
at our discretion, would permit any
refiner to seek a temporary waiver from
the MSAT benzene standard under
certain rare circumstances. This waiver
provision is similar to provisions in
prior fuel regulations. It is intended to
provide refiners relief in unanticipated
circumstances—such as a refinery fire or
a natural disaster—that cannot be
reasonably foreseen now or in the near
future.
Under this provision, a refiner could
seek permission to extend the deficit
carryover provisions of the proposal for
more than the one year already allowed
if it could demonstrate that the
magnitude of the impact was so severe
as to require such an extension. We are
proposing that the refiner would be
required to show that: (1) The waiver
would be in the public interest; (2) the
refiner was not able to avoid the
nonconformity; (3) it would meet the
proposed benzene standard as
expeditiously as possible; (4) it would
make up the air quality detriment
associated with the nonconforming
gasoline, where practicable; and (5) it
would pay to the U.S. Treasury an
amount equal to the economic benefit of
the nonconformity less the amount
expended to make up the air quality
detriment. These conditions are similar
to those in the RFG, Tier 2 gasoline
sulfur, and the highway and nonroad
diesel regulations, and are necessary
and appropriate to ensure that any
waivers that were granted would be
limited in scope.
As discussed, such a request would be
based on the refiner’s inability to
produce compliant gasoline at the
affected facility due to extreme and
unusual circumstances outside the
refiner’s control that could not have
been avoided through the exercise of
due diligence. The hardship request
would also need to show that other
avenues for mitigating the problem,
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such as the purchase of credits toward
compliance under the proposed credit
provisions, had been pursued and yet
were insufficient or unavailable.
Especially in light of the credit
flexibilities built into the proposed
overall program, we expect that the
need for additional relief would be rare.
b. Temporary Waivers Based on Extreme
Hardship Circumstances
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In addition to the provision for shortterm relief in extreme unforeseen
circumstances, we are also proposing a
hardship provision where a refiner
could receive an extension of the deficit
carryover provisions based on extreme
hardship circumstances. Such hardship
could exist based on severe economic or
physical lead time limitations of the
refinery to comply with the benzene
standard at the start of the program, and
if they were unable to procure sufficient
credits. A refiner seeking such hardship
relief under this proposed rule would
have to demonstrate that these criteria
were met. In addition to showing that
unusual circumstances exist that impose
extreme hardship in meeting the
proposed standard, the refiner would
have to show (1) best efforts to comply,
including through the purchase of
credits, (2) the relief granted under this
provision would be in the public
interest, (3) that the environmental
impact would be acceptable, and (4) that
it has active plans to meet the
requirements as expeditiously as
possible. Because such a demonstration
could not be made prior to the
development of the credit market, EPA
would not begin to consider such
hardship requests until August 1, 2010,
that is, until after the final precompliance reports are submitted.
Consequently, requests for such
hardship relief would have to be
received prior to January 1, 2011.
If hardship relief under these
circumstances was approved, we would
expect to impose appropriate conditions
to ensure that the refiner was making
best efforts to achieve compliance
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offsetting any loss of emission control
from the program through the deficit
carryforward provisions. We believe
that providing short-term relief to those
refiners that need additional time due to
hardship circumstances would help to
facilitate the adoption of the overall
MSAT program for the majority of the
industry. However, we do not intend for
hardship waiver provisions to
encourage refiners to delay planning
and investments they would otherwise
make. Again, because of the flexibilities
of the proposed overall program, we
expect that the need for additional relief
would be rare.
c. Early Compliance With the Proposed
Benzene Standard
We are also requesting comment on a
means for allowing refineries, under
certain conditions, to meet the proposed
benzene standard early in lieu of
MSAT1. In order to meet the proposed
benzene standard early, refiners would
need to meet several criteria similar to
those used in the past when EPA has
adjusted refinery baselines under the
MSAT1 program. Specifically, the
eligibility for such provisions would be
limited to refiners that have historically
had better than average toxics
performance, lower than average
benzene and sulfur levels, and a
significant volume of gasoline impacted
by the phase-out of MTBE as an
oxygenate. The result of not allowing
such early compliance could be less
supply of their cleaner fuel and more
supply of fuel with higher toxics
emissions, with a worsening of overall
environmental performance under
MSAT1. A refiner opting into such
provisions would not be allowed to
generate benzene credits on the affected
fuel prior to 2011, since an ability to
reduce benzene further would
presumably negate the need for an early
compliance option.
F. Technological Feasibility of Gasoline
Benzene Reduction
This section summarizes our
assessment of the feasibility for the
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refining industry to reduce benzene
levels in gasoline to an average of 0.62
vol% starting January 1, 2011. Based on
this assessment, we believe that it is
technologically feasible for refiners to
meet the benzene standard by the start
date using technologies that are
currently available.
We begin this section by describing
where benzene comes from and the
current levels found in gasoline. Next
we discuss the benzene reduction
technologies available to refiners today
and how they are expected to be used
to meet the proposed benzene standard.
Then we provide our analysis of the
lead time necessary for complying with
the benzene standard. All of these issues
are discussed in more detail in Chapters
6 and 9 of the Regulatory Impact
Analysis.
1. Benzene Levels in Gasoline
EPA receives information on gasoline
quality, including benzene levels, from
each refinery and importer in the U.S.
under the reporting requirements of the
RFG and CG programs. As discussed
earlier in this section, benzene levels
averaged 0.94 vol% for gasoline
produced in and imported into the U.S.
in 2003, which is the most recent year
for which complete data is available.
However, for individual refineries, daily
batch gasoline benzene levels and
annual average levels can vary
significantly from the national average.
As indicated earlier in describing our
decision-making process for the type
and level of gasoline benzene standard,
it is very important to understand how
current benzene levels vary by
individual refinery, by region, as well as
day-to-day by batch.
The variability in 2003 average annual
gasoline benzene levels by individual
refinery is shown in Figure VII.F–1.
This figure contains a summary of
annual average gasoline benzene levels
by individual refinery for CG and RFG
versus the cumulative volume of
gasoline produced.
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Figure VII.F–1 shows that the annual
average benzene levels of CG as
produced by individual refineries varies
from 0.29 to 4.01 vol%. Based on the
data in the figure, the volume-weighted
average benzene content for U.S. CG is
1.10 vol%. As expected, the annual
average benzene levels of RFG as
produced by individual refineries are
lower, ranging from 0.10 to 1.09 vol%.
The volume-weighted average benzene
content for U.S. RFG (not including
California) is 0.62 vol%.
The information presented for annual
average gasoline benzene levels does not
illustrate the very large day-to-day
variability in gasoline batches produced
by each refinery. We evaluated the
batch-by-batch gasoline benzene levels
for several refineries that produce both
RFG and CG, using information
submitted to EPA as part of the
reporting requirements for the RFG and
CG Anti-dumping Programs. One
refinery had no particular trend for its
CG benzene levels, with benzene levels
that varied from 0.1 to 3 vol%. That
same refinery’s RFG averaged around
0.95 vol% benzene, ranging from 0.05 to
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1.1 vol%. The second refinery had RFG
benzene levels that averaged around 0.4
vol% ranging from 0.1 to 1.0 vol%. Its
CG benzene levels averaged about 0.6
vol% with batches that ranged from 0.1
to 1.2 vol%. The batches for both RFG
and CG varied on a day-to-day basis
and, overall, by over an order of
magnitude. It is clear from our review of
batch-by-batch data submitted to EPA
that benzene variability is typical of
refineries nationwide.
There are several contributing factors
to the variability in refinery gasoline
benzene levels across all the refineries.
We will review these factors and
describe how each impacts batch-bybatch and annual average gasoline
benzene levels.
The first factor contributing to the
variability in gasoline benzene levels is
crude oil quality. Each refinery
processes a particular crude oil slate,
which tends to be fairly constant except
for seasonal changes that reflect changes
in product demand. Crude oil varies
greatly in aromatics content. Since
benzene is an aromatic compound, its
level tends to vary with the aromatics
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content of crude oil. For example,
Alaskan North Slope crude oil contains
a high percentage of aromatics. Refiners
processing this crude oil in their
refineries shared with us that their
straight run naphtha contains on the
order of 3 vol% benzene (the production
of naphtha is discussed further below).
This is one reason why the gasoline in
PADD 5 outside of California is high in
benzene. Conversely, refiners that
process very paraffinic crude oils (low
in aromatics) usually have a low amount
of benzene in their straight run naphtha.
Because crude oil supplies tend to be
constant over periods of months, crude
oil quality is not a major contributor to
day-to-day variations in benzene among
gasoline batches. However, because
crude oil supplies often vary from
refinery to refinery, differences in crude
quality are an important factor in the
variability among refineries.
The second factor contributing to the
variability in benzene levels is
differences in the types of processing
units and gasoline blendstocks among
refineries. If a refinery is operated to
rely on its reformer for virtually all of
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its octane needs—especially the type
that operates at higher pressures and
temperatures and thus tends to produce
more benzene—it will likely have a high
benzene level in its gasoline. Refineries
with a reformer and without a fluidized
catalytic cracking (FCC) unit are
particularly prone to higher benzene
levels, since they rely heavily on the
product of the reformer (reformate) to
meet octane needs. However, refineries
that can rely on other means for
boosting their gasoline octane can
usually rely less on the reformer and
can run this unit at a lower severity,
resulting in less benzene in their
gasoline pool. Examples of such other
octane-boosting refinery units include
the alkylation unit, the isomerization
unit and units that produce oxygenates.
Refiners may have these units in their
refineries, or in many cases, they can
purchase the gasoline blendstocks
produced by these units from other
refineries or third-party producers. The
blending of the products of these
processes—alkylate, isomerate, and
oxygenates—into the gasoline pool
provides a significant octane
contribution, which can allow refiners
to rely less on the octane from
reformate. Since refiners make
individual decisions about producing or
purchasing different blendstocks for
each refinery, this variation is another
important contributor to differences in
gasoline benzene content among
refineries. In addition, the variation in
gasoline blendstocks used to produce
different batches of gasoline is by far the
most important factor in the drastically
differing benzene levels among batches
of gasoline at any given refinery.
This practice by refiners of producing
or purchasing different blendstocks and
blending them in different ways to
produce gasoline is an integral and
essential aspect of the refining business.
Thus, in designing an effective benzene
control program, it is critical that
benzene levels be reduced while
refiners retain the ability to change
blendstocks (and crude supplies) as
needed from batch to batch and refinery
to refinery. We believe that the
proposed program accomplishes these
goals.
A third important source of variability
in existing benzene levels in gasoline is
the fact that many refiners are already
operating their refineries today to
intentionally reduce benzene levels in
their gasoline, while others are not. For
example, refiners that are currently
producing RFG must ensure their RFG
averages 0.95 vol% or less and is always
under the 1.3 vol% cap (see discussion
of the current toxics program in section
VII.C.5 above). Similarly, refiners
producing gasoline to comply the
California RFG program need to produce
gasoline with reduced benzene. These
refiners are generally using benzene
control technologies to actively produce
gasoline with lower benzene levels. If
they are producing CG along with the
RFG, their CG is usually lower in
benzene as well compared with the CG
produced by other refiners, since the
benzene control technology often affects
some of the streams used to blend CG.
In addition, some refiners add specific
refinery units such as benzene
extraction to intentionally produce
chemical-grade benzene. Benzene
commands a much higher price on the
chemical market compared to the price
of gasoline. For these refiners, the profit
from the sale of benzene pays for the
equipment upgrades needed to greatly
reduce the levels of benzene in their
gasoline. In most cases, refineries with
extraction units are marketing their lowbenzene gasoline in the RFG areas.
The use of these benzene control
technologies by some refiners
contributes to the variability in gasoline
benzene levels among refineries. The
use of these technologies can also
contribute to the batch-to-batch
variability in benzene levels. This is
because, as with different blendstocks,
refiners need to be able to change the
operating characteristics of these
technologies to meet varying needs in
gasoline quality. In addition, planned or
unexpected shut-downs of benzene
control equipment may result in
temporarily high batch benzene levels
relative to the normally low gasoline
levels when the unit is operating.
The variations in gasoline benzene
levels among refineries also lead to
variations in benzene levels among
regions of the country. Table VII.F–1
shows the average gasoline benzene
levels for all gasoline produced in (and
imported into) the U.S. by PADD for
2003. The information is presented for
both CG and RFG.
TABLE VII.F–1.—BENZENE LEVELS BY GASOLINE TYPE PRODUCED IN OR IMPORTED INTO EACH PADD IN 2003
PADD
1
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Conventional Gasoline .....................................................................................
Reformulated Gasoline ....................................................................................
Gasoline Average ............................................................................................
Table VII.F–1 shows that benzene
levels vary fairly widely across different
regions of the country. PADD 1 and 3
benzene levels are lower because the
refineries in these regions produce a
high percentage of RFG for both the
Northeast and Gulf Coast. Also, a
number of refineries in these two
regions are extracting benzene for sale
into the chemicals market, contributing
to the much lower benzene level in
these PADDs. It is interesting to note
that, in addition to RFG, CG benzene
levels are low in PADDs 1 and 3. There
are two reasons for this. First, some RFG
produced by refineries ends up being
sold as CG. Second, as mentioned
above, refiners that are reducing the
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PADD
2
PADD
3
PADD
4
PADD
5
0.84
0.60
0.70
1.39
0.82
1.28
0.94
0.56
0.87
1.54
n/a
1.54
1.79
n/a
1.79
benzene levels in their RFG generally
also impact the benzene levels in their
CG. In contrast, other parts of the U.S.
with little to no RFG production and
little extraction have much higher
benzene levels.
2. Technologies for Reducing Gasoline
Benzene Levels
a. Why Is Benzene Found in Gasoline?
To discuss benzene reduction
technologies, it is helpful to first review
some of the basics of refinery
operations. Refineries process crude oil
into usable products such as gasoline,
diesel fuel and jet fuel. For a typical
crude oil, about 50 percent of the crude
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CA
0.63
0.62
0.62
U.S.
1.11
0.62
0.94
oil falls within the boiling range of
gasoline, jet fuel and diesel fuel. The
rest of crude oil boils at too high a
temperature to be blended directly into
these products and therefore must be
cracked into lighter compounds.
Material that boils within the gasoline
boiling range is called naphtha. There
are two principal sources of naphtha.
The first is ‘‘straight run’’ naphtha,
which comes directly off of the crude oil
atmospheric distillation column.
Another principle source of naphtha is
that generated from the cracking
reactions. Each type of naphtha
contributes to benzene in gasoline.
Typically, little of the benzene in
gasoline comes from benzene naturally
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occurring in crude oil. Straight run
naphtha, which comes directly from the
distillation of crude oil, thus tends to
have a low benzene content, although it
can contain anywhere from 0.3 to 3
vol% benzene. While straight run
naphtha is in the correct distillation
range to be usable as gasoline, its octane
value is too low for blending directly
into gasoline. Thus, the octane value of
this material must be increased to
enable it to be used as a gasoline
blendstock.
The primary means for increasing the
octane value of naphtha (whether
straight run or from cracking processes)
is reforming. Reforming reacts the
heavier portion of straight run naphtha
(six-carbon material and heavier) over a
precious metal catalyst at a high
temperature. The reforming process
converts many of the naphtha
compounds to aromatic compounds,
which raises the octane of this reformate
stream to over 90 octane numbers.
(‘‘Octane number’’ is the unit of octane
value.) Since benzene is an aromatic
compound, it is produced along with
toluene and xylene, the other primary
aromatic compounds found in gasoline.
The reforming process increases the
benzene content of the straight run
naphtha stream from 0.3 to 3 vol% to 3
to 11 vol%.
There are two ways that benzene
levels increase in the reformer above the
benzene levels occurring naturally in
crude oil—the conversion of nonaromatic six-carbon hydrocarbons into
benzene, and the cracking of heavier
aromatic hydrocarbon compounds into
benzene.266 In the discussion below
about how benzene in the reformate
stream can be reduced, we elaborate
further about the opportunities that
refiners have to manage both of these
benzene-producing processes.
Three factors contribute to the wide
range in benzene levels in the reformate
stream, and these factors are important
in the decisions refiners would make in
response to the proposed benzene
control program. First, different
feedstocks contain different amounts of
benzene and different levels of benzene
precursors that are more or less capable
of being converted to benzene by the
reformer. Second, the type of reformer
being used affects how much benzene is
produced during the reforming process.
For example, refineries with the older,
higher pressure reformers tend to form
more benzene by cracking heavier
aromatics than refineries with newer,
lower pressure units. Third, the severity
with which the reformer is being
operated also affects benzene levels in
reformate. The greater the severity at
which the reformer is operated, the
greater the conversion of feedstocks to
aromatics (and the more hydrogen is
produced). However, more severe
operation shortens the time between the
catalyst regeneration events that the
reformer must periodically undergo.
Greater severity also lowers the gasoline
yield from this unit. Because refiners
balance these operation and production
factors individually at each refinery in
deciding on how severely to operate the
reformer, these decisions contribute to
the range of benzene levels found in
reformate from refinery to refinery.
In addition to benzene occurring in
the reformate stream, another source of
benzene in gasoline is naphtha
produced from cracking processes.
There are three primary cracking
processes in the refinery—the FCC unit,
the hydrocracker, and the coker. The
naphthas produced by these cracking
processes contain anywhere from 0.5 to
5 vol% benzene. The benzene in these
streams is typically formed from the
cracking of heavier aromatic compounds
into lighter compounds that can then be
blended into gasoline. The benzene
content of cracked streams is therefore
largely a function of the aromatics
content of the crude oil feedstocks and
the need of a particular refinery to
produce gasoline from heavier
feedstocks. As we discuss later, we do
not expect that benzene reductions from
these cracked naphthas would be a
major avenue for compliance with the
proposed benzene control program for
most refiners.
Finally, there are other intermediate
streams that contribute to benzene in
gasoline but that have such low benzene
content or are found in such low
volumes in gasoline that they are of very
limited importance in reducing benzene
levels. Examples of these are light
straight run naphtha and the oxygenates
MTBE and ethanol.
Table VII.F–2 summarizes the typical
ranges in benzene content and average
percentages of gasoline of the various
intermediate streams that are blended to
produce gasoline.
TABLE VII.F–2.—BENZENE CONTENT AND TYPICAL GASOLINE FRACTION OF VARIOUS GASOLINE BLENDSTOCKS
Typical
benzene level
(vol%)
Process or blendstock name
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Reformate ......................................................................................................................................................
FCC Naphtha .................................................................................................................................................
Alkylate ..........................................................................................................................................................
Isomerate .......................................................................................................................................................
Hydrocrackate ................................................................................................................................................
Butane ............................................................................................................................................................
Light Straight Run ..........................................................................................................................................
MTBE/Ethanol ................................................................................................................................................
Natural Gasoline ............................................................................................................................................
Coker Naphtha ...............................................................................................................................................
3–11
0.5–2
0
0
1–5
0
0.3–3
0.05
0.3–3
3
Average
volume in
gasoline
(percent)
30
36
12
4
3
4
4
3
3
1
Table VII.F–2 shows that the principal
contributor of benzene to gasoline is
reformate. This is due both to its high
benzene content and the relatively large
gasoline fraction that reformate
comprises of the gasoline pool. The
product stream from the reformer,
reformate, accounts for between 15 and
50 percent of the content of gasoline,
depending on the refinery (typically
about 35 percent.) For this reason and
as discussed below, reducing the
benzene in reformate is the primary
focus of the various benzene reduction
technologies available to refiners.
Control of benzene from the other
streams quickly becomes cost
prohibitive due to either the low
266 In the process of converting the straight run
naphtha into aromatics, a significant amount of
hydrogen is produced that is critical for the various
hydrotreating operations in refineries. As discussed
later, the impact on hydrogen production is an
important consideration in reducing benzene levels.
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depending on the refinery (typically
about 35 percent.) For this reason and
as discussed below, reducing the
benzene in reformate is the primary
focus of the various benzene reduction
technologies available to refiners.
Control of benzene from the other
streams quickly becomes cost
prohibitive due to either the low
concentration of benzene in the stream,
the low volume of the stream, or both.
b. Benzene Control Technologies
Related to the Reformer
There are several technologies that
reduce gasoline benzene by controlling
the benzene in the feedstock to and the
product stream from the reformer.267
One approach is to route the
intermediate refiner streams that have
the greatest tendency to form benzene in
a way that bypasses the reformer. This
approach is very important in benzene
control, but it is limited in its
effectiveness because it does not address
any of the naturally-occurring benzene
and some of the benzene formed in the
reformer. For this reason, refiners often
use a second category of technologies
that remove or destroy benzene,
including both the naturally occurring
benzene as well as that formed in the
reformer. These technologies are
isomerization, benzene saturation, and
benzene extraction. We discuss each of
these approaches to benzene reduction
below. The effectiveness of these
technologies in reducing the benzene
content of reformate varies from
approximately 60% to 96%. The actual
impact on an individual refinery’s
finished gasoline benzene content,
however, will be a function of many
different refinery-specific factors,
including the extent to which they are
already utilizing one of these
technologies.
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i. Routing Around the Reformer
The primary compounds that are
converted to benzene by the reforming
unit are the six-carbon hydrocarbon
compounds contained in the straight
run naphtha fed to the reformer. These
compounds, along with the naturallyoccurring benzene in this straight run
naphtha stream, can be removed from
the feedstock to the reforming unit using
the upstream distillation unit, bypassed
around the reforming unit, and then
blended directly into gasoline. Routing
267 The benzene reduction technologies are
discussed here in the context of the feasibility for
reducing the benzene levels of gasoline to meet a
gasoline benzene content standard. However, this
discussion applies equally to the feasibility of a
total air toxics standard, since we believe that
benzene control would be the only means that
refiners would choose in order to comply with such
a standard.
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these compounds around the reformer
prevents the formation of much of the
benzene in the reformer, though it does
not reduce the naturally-occurring
benzene.
For a typical refinery, the technology
to route the six-carbon material around
the reformer would likely require only
a small capital investment. Compared
with a scenario where all of this
material goes to the reformer, the
combined rerouted and reformate
streams would overall have about 60
percent less benzene, and finished
gasoline would have about 31 percent
less benzene. However, in most cases
this would not be sufficient to achieve
a 0.62 vol% benzene standard, and
some combination of the technologies
discussed next would also be needed.
ii. Routing to the Isomerization Unit
A variation of routing around the
reformer involves the isomerization of
the re-routed benzene precursors. Rather
than directly blending the rerouted
stream into gasoline, this stream can
first be processed in the isomerization
unit. This has two main advantages.
First, it increases the effectiveness of
benzene control, since the isomerization
process converts the naturally-occurring
benzene in this rerouted stream to
another compound. Second, it recovers
some of the octane otherwise lost by the
conversion of benzene.
The typical role of the isomerization
unit is to convert five-carbon
hydrocarbons from straight-chain to
branched-chain compounds, thus
increasing the octane value of this
stream. If the isomerization unit at a
refinery has sufficient additional
capacity to handle the rerouted sixcarbon hydrocarbons, that stream can
also be sent to this unit, where the
benzene present in that stream would be
saturated and converted into another
compound (cyclohexane). (This benzene
saturation process is similar to what
occurs in a dedicated benzene
saturation unit, as described below.)
Compared to a scenario where all this
material goes to the reformer, routing
the six-carbon compounds to the
isomerization unit in this manner can
reduce the benzene levels in the
combined rerouted and reformate
streams by about 80 percent. The option
of isomerization is currently available to
those refineries with sufficient capacity
in an existing isomerization unit to treat
all of the six-carbon material.
iii. Benzene Saturation
The function of a benzene saturation
unit is to react hydrogen with the
benzene in the reformate (that is, to
saturate the benzene) in a dedicated
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reactor, converting the benzene to
cyclohexane. Because hydrogen is used
in this process, refiners that choose this
technology need to ensure that they
have a sufficient source of hydrogen.
Refiners cannot afford to saturate other
aromatic compounds present in their
reformate as it would cause too great an
octane loss. Thus, it is necessary to
separate a six-carbon stream, which
contains the benzene, from the rest of
reformate, and only feed the six-carbon
stream to the benzene saturation unit.
This separation is done with a
distillation unit called a reformate
splitter placed just after the reformer.
There are two vendors that produce
benzene saturation units. UOP produces
a technology named Bensat. There are at
least six Bensat units operating in the
U.S. today and many more around the
world. CDTech licenses another,
somewhat newer technology for this
purpose called CDHydro. There are six
CDHydro units operating today, mostly
outside of the U.S. Benzene saturation
can reduce benzene in the reformate by
about 96 percent.
iv. Benzene Extraction
Extraction is a technology that
chemically removes benzene from
reformate. The removed benzene can be
sold as a high-value product in the
chemicals market. To extract only
benzene from the reformate, a reformate
splitter is installed just after the
reformer to separate a benzene-rich
stream from the rest of the reformate.
The benzene-rich stream is sent to an
extraction unit which separates the
benzene from the rest of the
hydrocarbons. Since the benzene must
be sufficiently concentrated before it
can be sold on the chemicals market, a
very thorough distillation step is
incorporated with the extraction step to
concentrate the benzene to the
necessary purity. Where it is economical
to use, benzene extraction can reduce
benzene levels in the reformate by 96
percent.
There are two important
considerations refiners have with
respect to using benzene extraction. The
first is the price of chemical grade
benzene. If the price of chemical grade
benzene is sufficiently higher than the
price of gasoline, benzene extraction can
realize an attractive return on capital
invested and is often chosen as a
technology for achieving benzene
reduction. The difference in price
between benzene and gasoline has been
significantly higher than its historic
levels during the last few years. While
we expect that this difference will
return closer to the lower historic levels
by the time the proposed program
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would be implemented, the difference
in prices should still be sufficient to
make extraction a very cost-effective
technology for reducing gasoline
benzene levels. A more detailed
discussion about benzene prices is
contained later in this preamble (section
IX) and in Chapter 9 of the RIA.
The other consideration in using
benzene extraction is the distance that
a refinery is from the markets where
benzene is used as a chemical feedstock.
Transportation of chemical grade
benzene requires special hazardousmaterials precautions, including
protection against leaks. Certain
precautions are also necessary to
preserve the purity of the benzene
during shipment. These special
precautions are costly for shipping
benzene over long distances. Thus if a
refinery were located far from the
chemical benzene markets, the
economics for using extraction would be
much less attractive compared to that of
refiners located near benzene markets.
The result has been that chemical
grade benzene production has been
limited to those refineries located near
the benzene markets. This includes
refineries on the Gulf and on the East
Coast and to a limited extent, several
refineries in the Midwest. This could
change if the very high benzene prices
in 2004 and the beginning of 2005 were
to continue, instead of returning to
lower historical levels. However, even if
benzene prices remain high by the time
that a benzene control standard would
take effect, refineries located away from
the benzene markets may be concerned
that the higher benzene prices may not
be certain enough for the long term to
warrant investment in extraction. Our
analysis for today’s proposal
conservatively assumes that only
refineries on the Gulf and East coasts
would choose to use benzene extraction
to lower their gasoline benzene levels.
Despite some existing extraction units
in the Midwest, the benzene market
there is small and no additional benzene
extraction is assumed to occur there.
c. Other Benzene Reduction
Technologies
We are aware of other, less attractive
technologies capable of achieving
benzene reductions in gasoline. These
technologies tend to have more serious
impacts on other important refinery
processes or on fuel quality and are
generally capable of only modest
benzene reductions. We do not
currently have sufficient information
about how widely these approaches are
or could be utilized or their potential
costs, and in our modeling we have not
assumed that refiners would use them.
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However, because they may be feasible
in some unique situations, we mention
these potential gasoline benzene
reduction approaches here.
One of these less attractive
opportunities for additional benzene
reduction would be for refiners to
capture more of the reformate benzene
in the reformate splitter and send this
additional benzene to the saturation
unit. Refiners attempt to minimize both
the capital and operating costs when
splitting a benzene-rich stream out of
the reformate stream for treating in a
benzene saturation unit. To do this, they
optimize the distillation cut between
benzene and toluene, thus achieving a
benzene reduction of about 96 percent
in the reformate while preserving all but
about 1 percent of the high-octane
toluene. However, if a refiner were to be
faced with a dire need for additional
benzene reductions, it could change its
distillation cut to send the last 4 percent
of the benzene to the saturation unit.
Since this cut would also bring with it
more toluene than the normal optimized
scenario, this toluene would also be
saturated, resulting in a larger loss in
octane and greater hydrogen
consumption.
Some refineries with hydrocracking
units may have another means of further
reducing the gasoline benzene levels.
They may be able to reduce the benzene
content of one of the products of the
hydrocracker, the light hydrocrackate
stream. Today, light hydrocrackate is
normally blended directly into gasoline.
Light hydrocrackate contains a moderate
level of benzene, although its
contribution to the gasoline benzene
levels is significant only in those
refineries with hydrocrackers. Light
hydrocrackate could be treated by
routing this stream to an isomerization
unit, similar to how refiners isomerize
the six-carbon straight run naphtha as
discussed above. Alternatively, refiners
could use additional distillation
equipment to cut the light
hydrocrackate more finely. In this way,
more of the benzene could be shifted to
the ‘‘medium’’ hydrocrackate stream,
which in most refineries is sent to the
reformer and thus would be treated
along with the reformate.
Another way that we believe some
refiners could further reduce their
benzene levels would be to treat the
benzene in natural gasoline. Many
refiners, especially in PADDs 3 and 4,
blend some light gasoline-like material,
which is a by-product of natural gas
wells, into their gasoline. In most cases,
we believe that this material is blended
directly into gasoline. Because the
benzene concentration in this stream is
not high, it would be costly to treat the
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stream to reduce benzene. However,
there could be other reasons that
refiners might find compelling for
treating this stream. First, since its
octane is fairly low to begin with, it
could be fed to the reformer and its
benzene would be treated in the
reformate, along with the benefit of
improving the octane quality of this
stream. Second, refiners producing lowsulfur gasoline under the gasoline sulfur
program may not be able to easily
tolerate the sulfur from this stream if it
were blended directly into gasoline.
Thus, if they treat this stream in the
reformer, it would undergo the
hydrotreating (desulfurization) that is
necessary for all streams fed to the
reformer. Overall, we do not have
sufficient information to conclude
whether treating natural gasoline might
become more attractive in the future.
Another approach to benzene
reduction that we believe could be
attractive in certain unique
circumstances relates to the benzene
content in naphtha from the fluidized
catalytic cracker, or FCC unit. As shown
in Table VII.F–2, FCC naphtha contains
less than 1 percent benzene on average.
Despite the very low concentration of
benzene in FCC naphtha, the large
volumetric contribution of this stream to
gasoline results in this stream
contributing a significant amount of
benzene to gasoline as well. There are
no proven processes which treat
benzene in FCC naphtha. This is
because its concentration is so low as
well as because FCC naphtha contains a
high concentration of olefins.
Segregating a benzene-rich stream from
FCC naphtha and sending it to a
benzene saturation unit would saturate
the olefins in the same boiling range,
resulting in an unacceptable loss in
octane value. Also, some refiners
operate their FCC units today more
severely to improve octane, an action
that also increases benzene content.
Conceivably, refiners could redesign
their FCC process (change the catalyst
and operating characteristics) to reduce
the severity and produce slightly less
benzene. We do not have sufficient
information to know whether many
refiners are already operating at high
FCC severity and thus have the potential
to reduce benzene by reducing that
severity.
We request comment on our
assessment of benzene reduction
approaches, including data related to
the current or potential usage and
potential effectiveness of each approach.
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d. Impacts on Octane and Strategies for
Recovering Octane Loss
All these benzene reduction
technologies affect the octane of the
final gasoline. Regular grade gasoline
must comply with a minimum 87 octane
(R+M)/2 rating (or a sub-octane rating of
86 for driving in altitude), while
premium grade gasoline must comply
with an octane rating which ranges from
91 to 93 (R+M)/2. Gasoline must meet
these octane ratings to be sold as
gasoline at retail. Routing the benzene
precursors around the reformer reduces
the octane of the six-carbon compound
stream, which normally exits the
reformer with the rest of the reformate.
Without these compounds in the
reformate, a loss of octane in the
gasoline pool of about 0.14 octane
numbers typically occurs. If this
rerouted stream can be sent to an
isomerization unit, a portion of this lost
octane can be recovered, provided that
sufficient capacity remains in that unit
to continue treating the five-carbon
naphtha compounds. Benzene
saturation and benzene extraction both
affect the octane of reformate and
therefore the gasoline pool. Benzene
saturation typically reduces the octane
of gasoline by 0.24 octane numbers, and
benzene extraction typically reduces the
octane by 0.14 octane numbers.
Refiners can recover the lost octane in
a number of ways. First, the reformer
severity can be increased. However, if
the refiner is reducing benzene through
precursor rerouting or saturation, this
strategy can be somewhat
counterproductive. This is because
increased severity increases the amount
of benzene in the reformate and thus
increases the cost of saturation and
offsets some of the benzene reduction of
precursor rerouting. Increasing reformer
severity would also decrease the
operating cycle life of the reformer,
requiring more frequent regeneration.
However, where benzene extraction is
used, increased reformer severity can
improve the economics of extraction
because not only is lost octane replaced
but the amount of benzene extracted is
increased. Again, operating the reformer
more severely would have the negative
impact of shortening the reformer’s
operating cycle between regeneration
events.
Lost octane can also be recovered by
increasing the activity of other octaneproducing units at the refinery. As
discussed above, saturating benzene in
the isomerization unit loses the octane
value of that benzene, but octane is
increased by the simultaneous
formation of branch-chain compounds.
Also, many refineries produce a high-
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octane blendstock called alkylate.
Alkylate is produced by reacting normal
butane and isobutane with isobutylene
over an acid catalyst. Not only is this
stream high in octane, but it converts
compounds that are too volatile to be
blended in large amounts into the
gasoline pool into heavier compounds
that can be readily blended into
gasoline. If the refinery is short of
feedstocks for alkylate, then the
operations of the FCC unit, which is the
principal producer of these feedstocks,
can be adjusted to produce more of the
feedstocks for the alkylate unit,
increasing the availability of this high
octane blendstock.
Octane can also be increased by
purchasing high-octane blendstocks and
blending them into the gasoline pool.
For example, some refiners with excess
octane production capacity market high
octane blendstocks such as alkylate or
aromatics such as toluene. Oxygenates,
such as ethanol, can also be blended
into the gasoline pool. Other oxygenates
such as methyl tertiary butyl ether
(MTBE), ethyl tertiary butyl ether
(ETBE), tertiary amyl methyl ether
(TAME), and other ethers are sometimes
used. The availability and cost of
oxygenates for octane replacement vary
according to material prices as well as
state and federal policies that either
encourage or discourage their use. (For
example, the Energy Policy Act of 2005
requires an increase in the volume of
renewable fuels, including ethanol,
which are blended into gasoline).
e. Experience Using Benzene Control
Technologies
All of the benzene reduction
technologies and octane generating
technologies described above have been
demonstrated in refineries in the U.S.
and abroad. All four of these
technologies have been used for
compliance purposes for the federal
RFG program, which has required that
benzene levels be reduced to an average
of 0.95 vol% or lower since 1995.
According to the Oil and Gas Journal’s
worldwide refining capacity report for
2003, there were 27 refineries in the
U.S. with extraction units. Those
refineries that chose extraction often
reduced their benzene to levels well
below 0.95 vol% because of the value of
benzene as a chemical feedstock, as
discussed above. Once a refiner invests
in extraction, they have a strong
incentive to maximize benzene
production and thus the availability of
benzene to sell to the chemical market,
often reducing gasoline benzene more
than is required by regulation. The RFG
program also led to the installation of a
small number of benzene saturation
units in the Midwest to produce RFG for
the markets there. California has its own
RFG program which also put into place
a stringent benzene standard for the
gasoline sold there. The Oil and Gas
Journal’s Worldwide Refining Report
shows that four California refineries
have benzene saturation units. If we
assume that those RFG and California
refineries that do not have extraction or
saturation units are routing their
precursors around their reformer, then
there are 28 refineries using benzene
precursor rerouting as their means to
reduce benzene levels. Thus, these
technologies have been demonstrated in
many refineries since the mid-1990s in
the U.S. and are considered by the
refining community as commercially
proven technologies.
Worldwide experience provides
further evidence of the commercial
viability of these benzene control
technologies. A vendor of benzene
control technology has shared with us
how the refining companies in other
countries have controlled the benzene
levels of their gasoline in response to
the benzene standards put in place
there. In Europe, benzene control is
typically achieved by routing the
benzene precursors around the reformer
and feeding that rerouted stream to an
isomerization unit. In Japan, much of
the benzene is extracted from gasoline
and sold to the chemicals market.
Finally, in Australia and New Zealand,
refiners tend to use benzene saturation
to reduce the benzene levels in their
gasoline.
f. What Are the Potential Impacts of
Benzene Control on Other Fuel
Properties?
With the complex nature of modern
refinery operations, most changes to fuel
properties affect other fuel properties to
some degree. In the case of benzene
control, the ‘‘ripple effects’’ on other
fuel properties tends to be limited.
However, as discussed above, the
reduction in benzene content that we
are proposing in this rule, depending on
how it is accomplished, would in most
cases slightly reduce the overall octane
of the resulting gasoline. Refiners would
likely compensate by increasing the
volume of reformate (other aromatics)
blended into the gasoline, requiring a
small increase in reformer severity and
energy inputs. Some analysis of gasoline
property survey data suggests that as
benzene is reduced in gasoline, other
aromatics may increase somewhat to
help compensate.
Another option refiners might
consider in response to the proposed
rule is match-blending ethanol to make
up octane and increase supply volume.
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This has been done for several years
with MTBE as an economical way to
meet toxics performance requirements
and octane targets for RFG. Like MTBE,
ethanol has a relatively high blending
octane, and is already added in many
markets to take advantage of tax benefits
or to support local suppliers. Since the
use of ethanol is being encouraged in
the recently-enacted energy legislation,
refiners will likely seek to capture the
octane benefits as part of their process,
which could help offset the octane loss
some refiners will see as a result of
benzene reduction processes.
Furthermore, to the extent that current
MTBE production is shifted to
production of isooctene, isooctane, and
alkylate, these compounds would be
available as high-octane, low-benzene
gasoline blendstocks.
Finally, refiners may blend in
isomerate or alkylate, which are very
‘‘clean’’ gasoline blendstocks, thereby
reducing the levels of ‘‘dirtier’’ gasoline
blendstocks, and reducing overall
sulfur, olefins, and aromatics. We do not
anticipate major changes in other fuel
properties due to reductions in benzene.
Our modeling of the emissions impacts
of the proposed benzene standard does
account for the modest changes in other
fuel properties. As discussed in section
V of this preamble and Chapter 2 of the
RIA, this emissions modeling indicates
that the proposed benzene standard has
negligible impacts on the emissions of
other mobile source air toxics.
3. Feasible Level of Benzene Control
A key aspect of our selection of the
level of the proposed average benzene
standard of 0.62 vol% was our
evaluation of the benzene levels
achievable by individual refineries. Our
modeling analyses, which combine our
understanding of technological and
economic factors, is summarized in
section IX below and discussed in detail
in Chapter 9 of the RIA. Later in this
section we summarize our conclusions
about the overall feasibility of the
program in terms of the requirements of
the Clean Air Act.
We assessed the benzene levels
achievable for each refinery, assuming
that each refinery pursued the most
stringent form of reformate benzene
control available to it—installing either
benzene saturation or extraction units.
Based on this assessment, we project
that the most stringent benzene level
achievable on average for all U.S.
gasoline would be 0.52 vol%
benzene.268 As discussed above,
268 This analysis is within the constraints of our
modeling and the refinery-specific information
available to us at the time of this proposal.
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however, a standard at this level would
require significant investment at
essentially all refineries—that is, nearuniversal installation of either benzene
saturation or benzene extraction
capability. As discussed in section IX
below, this would be a very expensive
result—costing about three times more
than the proposed program—that we do
not believe would be reasonable when
costs are taken into account.
Furthermore, the model projects that
all refineries would use optimal
combinations of actual benzene
reductions and/or credit purchases and
would meet the average standard
without going beyond the primary
technologies of reformate benzene
reduction discussed earlier in this
section. To reach this conclusion, our
model assumes a fully utilized credit
trading program (that is, each refiner is
assumed to minimize its average costs
and to freely trade credits among
companies so that all credits generated
are used). Although the assumption of a
fully utilized credit trading program is
appropriate for our modeling purposes,
it is very possible that this would not
occur in practice. For example, some
refiners might choose to hold onto
credits that they generate, saving them
for potential ‘‘emergencies’’ when
unexpected events would otherwise
cause noncompliance with the benzene
standard.
Given the high cost of control for
some refineries and the potential that
credit trading would be less-than-fully
utilized, we have looked at standards
less stringent than 0.52 vol% that might
be feasible, considering cost. Based on
our modeling, we believe that with the
proposed ABT program all gasoline
could be produced at the proposed
average level of 0.62 vol% without
extreme economic consequences. We
believe that sufficient credits would be
generated such that refineries facing the
highest costs of benzene control would
have sufficient access to credits and
would not need to turn to cost
prohibitive technologies.
From a strict feasibility standpoint,
we have also assessed whether all
refineries could meet the proposed
benzene level in cases where sufficient
credits were not available to every
refinery that might want them. We
found that, despite the application of
maximum reformate benzene control in
the refinery model to all refineries, the
analysis concluded that 13 refineries
would still have benzene levels that
exceeded a 0.62 benzene level, with one
refinery as high as 0.77 vol% benzene.
We have evaluated how these 13
refineries might use the other, less
attractive benzene control technologies
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discussed above (assuming that an ABT
option is not available to them).
The approach of capturing more of the
reformate benzene in the reformate
splitter and sending this additional
benzene to the saturation unit would
allow 7 of the 13 challenged refineries
to reach the 0.62 vol% level. Then,
those refineries with a hydrocracker or
a coker could reduce the benzene
content of the light hydrocrackate or
coker stream. This step would allow 5
more refineries to reach the target level.
Finally, the treatment of benzene in
natural gasoline would bring the
remaining 1 refinery to the 0.62 vol%
level or below. (Because of our lack of
information about the potential for
reducing the severity of the FCC unit,
and because we do not believe that
reducing the benzene level of FCC
naphtha is feasible, we did not consider
FCC options in this analysis.) Again, we
expect that at the proposed standard
level of 0.62 vol% in the context of the
proposed ABT program, all refineries
would be able to comply. This analysis
demonstrates that there are options,
although extreme and costly, for
challenged refineries even if the ABT
program does not fully function as
projected.
4. Lead Time
Our proposal for the gasoline benzene
standard to begin on January 1, 2011
would allow about four years after we
expect the rulemaking to be finalized for
refiners to comply with the program’s
requirements. As discussed below, we
believe that four years of lead time
would allow refiners sufficient time to
install the capital equipment they
would need to lower their benzene
levels, and would also allow this
program to avoid significant conflict
with other fuel programs being
implemented around the same time. In
addition, the ABT program would allow
the industry to phase in the program,
through the early credit provisions, so
that significant benzene reductions
would occur earlier than the program
start date. The credits earned could
allow the investment in higher capital
cost and less cost-effective technologies
to be delayed relative to the program
start date.
In recent years, the implementation of
the gasoline sulfur and highway diesel
sulfur programs has provided an
opportunity to observe the response of
the refining industry to major fuel
control requirements. Many refiners
have demonstrated their ability to make
very large, expensive sulfur control
modifications to their refineries in less
than four years, and in some cases
significantly less. It is helpful to
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compare this sulfur control experience
with the types of technologies refiners
would use to reduce benzene.
Refiners could implement approaches
to benzene control that require very
little or no capital equipment, including
routing of benzene precursors around
the reformer and the use of an existing
isomerization unit, with very little lead
time requirements. We believe that
approaches using moderately complex
capital equipment, including improving
the effectiveness of precursor rerouting
and expanding existing extraction
capacity, would generally require one to
two years of lead time. Projects that
involve the installation of new
equipment, including benzene
saturation and extraction units, require
more time, generally two to three years.
This includes time for the equipment
installation as well as related offsite
equipment and any necessary capital
equipment for production of hydrogen
or high-octane blendstocks. Of all the
benzene control approaches, benzene
extraction is closest in scope and
complexity to the technologies the
industry is using for fuel sulfur control.
In addition to the time needed for
planning and installing the extraction
unit and related equipment, extraction
also requires time to install additional
facilities for storing extracted benzene
and for loading it for transport. Thus, as
with the earlier programs, we believe
the refiners choosing to add a benzene
extraction unit could in some cases
need as much as four years to complete
the project. Overall, we believe that four
years of lead time would ensure that all
refiners would have sufficient time to
comply, regardless of the benzene
control technology they select.
Another factor in selecting an
appropriate date to begin the program is
the timing of the implementation of
other large fuel control programs,
especially the Nonroad Diesel rule.269
The 15 ppm sulfur standard mandated
by the Nonroad Diesel Fuel program
applies to nonroad diesel fuel in 2010
and to locomotive and marine diesel
fuel in 2012. Refiners modifying their
refineries to produce either ultra low
sulfur nonroad or locomotive and
marine diesel fuel will do so during the
several years prior to 2010 and 2012.
For each of those start dates, there is a
progression of actions which includes
269 The months leading up to January 2010 will
also be when several small refiners and refiners that
were granted hardship relief will be implementing
their gasoline sulfur programs. We believe that any
serious interference among implementation projects
that individual refiners might demonstrate during
this time period could be addressed under the small
refiner or general hardship provisions of the
proposed rule.
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planning, design, construction and startup all during the four year run-up
toward the start date of the program. For
example, the engineering and
construction (E&C) industry will be
busy designing and constructing each of
the units that will be installed. Different
portions of the E&C industry will be
engaged at specific periods of time
leading up to the time that the unit is
started up. For this reason, staggering
the start year of this benzene fuel
standard with the start years for the
Nonroad Diesel program would help to
avoid excessive demand on specific
parts of the E&C industry. The
staggering of today’s proposed
program’s start date with those of the
Nonroad Diesel program may also help
refiners that might be seeking to acquire
capital through banks or other lending
institutions by spreading out the
requests.
We believe that the proposed
implementation date of January 1, 2011
would minimize overlap and possible
interference with the implementation of
the Nonroad Diesel rule.
Implementation of the proposed
benzene standard one year earlier or one
year later would overlap directly with
one of the two Nonroad Diesel
implementation dates. We also believe
that the additional year of lead time,
compared to a 2010 start date, would
make the program more effective.
Because we expect that the proposed
ABT program would encourage many
refiners to reduce benzene levels early
whenever possible, we believe that
significant benzene reductions would
occur prior to 2011. We discuss this
expected early benzene reduction
further as a part of the description of the
proposed ABT program in section VII.D
above.
For these reasons, we are proposing
that the gasoline benzene standard be
implemented beginning January 1, 2011.
We request comment on the issue of
lead time, including data supporting
four years or a different length of time.
above would be particularly attractive to
small refiners for implementing into
their refineries. These are benzene
precursor rerouting, and, if the refinery
has an isomerization unit, routing the
benzene precursors to the isomerization
unit. These technologies would be
attractive to small refiners because they
would require little or no capital
investments to implement for reducing
their gasoline benzene levels. Therefore,
the per-gallon cost of these two
technologies is about the same as that
for large refineries.
Smaller refineries tend to have fewer
process units and blending streams,
which generally also means that they
will have fewer options for recovering
lost octane. For example, these
refineries are less likely to have an
alkylation unit. An alkylation unit gives
refiners short on octane the option to
change the operations of their FCC unit
to make more olefins and then send the
appropriate olefins to their alkylation
unit to produce more of that high octane
blendstock. This is not an option for
several of the small refiners that do not
have an alkylation unit. Also, small
refineries are more likely to have a
higher pressure reforming unit. The
higher pressure reformer units tend to
produce more benzene from the
cracking of heavier aromatic compounds
and will tend to do this more as their
severity is increased. A higher pressure
reformer also has a more difficult
regeneration cycle and shorter cycle
lengths as it is operated more severely.
Thus, while other refiners with lower
pressure units may be able to increase
the severity of their reformers to make
more octane without producing much
more benzene and greatly reducing the
cycle lengths of their reformers, many of
the small refiners may not have as much
flexibility in this area. In any event,
these greater technological challenges
can be offset somewhat where it is
economical to purchase high octane
blendstocks or oxygenates from other
refiners or from the petrochemical
industry.
5. Issues
b. Imported Gasoline
Although the majority of petroleum
products in the U.S. are made from
imported crude oil, only about five
percent of the gasoline consumed in this
country was imported as finished
gasoline in 2003. This imported fuel is
approximately half RFG and half CG,
and had an average benzene content of
0.8% volume in 2003. No batches of
imported gasoline had a benzene level
above 2.4%. Over 90% of the imported
gasoline was delivered into the East
Coast and Florida, with about 5%
arriving on the West Coast, and the
a. Small Refiners
Small refiners are technically capable
of realizing a similar benzene reduction
from their gasoline as large refiners.
Because of economies of scale, however,
some of the benzene control
technologies which would be more
affordable for larger refineries would be
much more challenging and more
expensive for small refiners. This is due
to the poorer economies of scale that the
small refiners are faced with installing
capital into their refineries. Two of the
benzene control technologies discussed
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remainder being brought into other
regions of the country. The origin of the
majority of this gasoline was Canada
(40%), Western Europe (31%), and
South America (17%).
Since imported finished gasoline is
not processed in a domestic refinery,
where refiners would be taking steps to
meet the proposed benzene standard,
importers would be affected in other
ways. Importers would most likely
either begin to purchase gasoline that is
low enough in benzene to meet the
standard, or they would continue to
import gasoline with benzene at current
levels but purchase credits to cover the
fuel being above the standard. As shown
above, over 70 percent of imported
gasoline comes from countries that have
already set benzene limits on their
gasoline. As a result, we believe that
gasoline with some degree of benzene
control will be easily available for
importers to market. In some cases, we
also expect that some foreign refiners
may produce for export some fraction of
their gasoline to meet our proposed 0.62
vol% average standard benzene. This
would provide importers further options
in the U.S. gasoline market.
G. How Does the Proposed Fuel Control
Program Satisfy the Statutory
Requirements?
As discussed earlier in this section,
we have concluded that the most
effective and appropriate program for
MSAT emission reduction from gasoline
is a benzene control program. Today’s
action proposes such a program, with an
average benzene content standard of
0.62 vol% and a specially-designed
averaging, banking, and trading
program. In section VII.F above, we
summarize our evaluation of the
feasibility of the proposed program, and
in section IX.A we summarize our
evaluation of the costs of the program.
The analyses supporting our
conclusions in these sections are
discussed in detail in Chapters 6 and 9
of the RIA.
Taking all of this information into
account, we believe that a program more
stringent than the proposed program
would not be feasible, taking into
consideration cost. As we have
discussed, making the standard more
stringent would require more refiners to
install the more expensive benzene
control equipment, with very little
improvement in benzene emissions.
Also, we have shown that related costs
increase very rapidly as the level of the
standard is made more stringent.
Conversely, while it would provide
significant benzene emission
reductions, we are concerned that a
somewhat less stringent national
average standard than the proposed 0.62
vol% (e.g., 0.65 or 0.70 vol%) would not
satisfy our statutory obligation for the
most stringent standard feasible
considering cost and other factors.
Furthermore, such standards would not
accomplish several important
programmatic objectives as discussed in
section VII.C.
We have also considered energy
implications of the proposed program,
as well as noise and safety, and we
believe the proposed program would
have very little impact on any of these
factors. Analyses supporting these
conclusions are also found in Chapter 9
of the RIA. We carefully considered lead
time in establishing the stringency and
timing of the proposed program (see
section VII.F above).
Consequently, we believe that the
proposed program would meet the
requirements of section 202(l) of the
Clean Air Act, reflecting ‘‘the greatest
degree of emission reduction achievable
through the application of technology
which is available, taking into
consideration * * * the availability and
costs of the technology, and noise,
energy, and safety factors, and lead
time.’’
energy used for benzene extraction. Our
modeling of increased energy use
indicates that the process energy used
by refiners to produce gasoline would
increase by about one percent. Overall,
we believe that the proposed rule would
result in no significant adverse energy
impacts.
The proposed gasoline benzene
provisions would not affect the current
gasoline distribution practices.
We discuss our analysis of the energy
and supply effects of the proposed
gasoline benzene standard further in
section IX of this preamble and in
Chapter 9 of the Regulatory Impact
Analysis.
The fuel supply and energy effects
described above would be offset
substantially by the positive effects on
gasoline supply and energy use of the
proposed gas can standards also
proposed in today’s action. These
proposed provisions would greatly
reduce the gasoline lost to evaporation
from gas cans. This would in turn
reduce the demand for gasoline,
increasing the gasoline supply and
reducing the energy used in producing
gasoline.
H. Effect on Energy Supply, Distribution,
or Use
This rule is not a ‘‘significant energy
action’’ as defined in Executive Order
13211, ‘‘Actions Concerning Regulations
That Significantly Affect Energy Supply,
Distribution, or Use’’ (66 FR 28355 (May
22, 2001)) because it is not likely to
have a significant adverse effect on the
supply, distribution, or use of energy. If
promulgated, the gasoline benzene
provisions of the proposed rule would
shift about 22,000 barrels per day of
benzene from the gasoline market to the
petrochemical market. This volume
represents about 0.2 percent of
nationwide gasoline production. The
actual impact of the rule on the gasoline
market, however, is likely to be less due
to offsetting changes in the production
of petrochemicals, as well as expected
growth in the petrochemical market
absent this rule. The major sources of
benzene for the petrochemical market
other than reformate from gasoline
production are also derived from
gasoline components or gasoline
feedstocks. Consequently, the expected
shift toward more benzene production
from reformate due to this proposed rule
would be offset by less benzene
produced from other gasoline
feedstocks.
The rule would require refiners to use
a small additional amount of energy in
processing gasoline to reduce benzene
levels, primarily due to the increased
I. How Would the Proposed Gasoline
Benzene Standard Be Implemented?
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This section discusses the details
associated with meeting the proposed
0.62 vol% benzene standard.
1. General Provisions
a. What Are the Implementation Dates
for the Proposed Program?
We are proposing that refiners and
importers would achieve compliance
with the requirements of the proposed
benzene program beginning with the
annual averaging period beginning
January 1, 2011. Refineries with
approved benzene baselines could
generate early credits from June 1, 2007,
through December 31, 2010. Refineries
and importers could generate standard
credits beginning with the annual
averaging period beginning January 1,
2011, provided that the average benzene
content of the gasoline they produce or
import during the year was less than
0.62 vol% benzene.
Approved small refiners would be
allowed to delay compliance with the
0.62 vol% standard until the annual
averaging period beginning January 1,
2015. They could, however, generate
early credits beginning June 1, 2007
through December 31, 2014, provided
that they had an approved benzene
baseline. They would be able to generate
standard credits beginning January 1,
2015.
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b. Which Regulated Parties Would Be
Subject to the Proposed Benzene
Standards?
Domestic refiners and importers
would be subject to the proposed
standards. We are proposing that each
refinery of a refiner must meet the
standard, and all associated
requirements, individually. Refinery
grouping, or aggregation, as allowed in
the Anti-dumping and MSAT1 program
for CG, would not be permitted for
purposes of complying with the
proposed benzene standard (although
the ABT provisions provide similar
flexibility, and the credit generation and
transfer provisions would perform
basically the same functions). For an
importer, we are proposing that the
requirements apply to the entire volume
imported during the averaging period
regardless of import locations or
sources. In addition, where a company
has both refinery and import operations,
each operation would have to achieve
its own compliance with the 0.62 vol%
benzene standard. We are proposing
that those who only added oxygenate or
butane to gasoline or gasoline blending
stock would not be subject to the
proposed standards for that gasoline
unless they also added other blending
components to the blend. This would be
similar to the current treatment of these
entities and their gasoline under the
RFG, Anti-dumping and MSAT1
programs, where specialized accounting
and calculation procedures are
specified. In these cases, the refinery (or
importer) that produces gasoline or
gasoline blendstock includes the
oxygenate in its own compliance
determination. We are proposing that
this practice would continue under
today’s program. Transmix processors
would not be subject to the proposed
requirements for gasoline produced
from transmix, but gasoline produced
from transmix to which other
blendstocks were added would be
subject to the proposed benzene
standard.
We are proposing that all gasoline
produced by foreign refineries for use in
the United States would be included in
the compliance and credit calculation of
the importer of record. Under the Antidumping and MSAT1 rules, as well as
the gasoline sulfur requirements,
additional requirements applicable to
foreign refiners who chose to comply
with those regulations separately from
any importer were included to ensure
that enforcement of the regulation at the
foreign refinery would not be
compromised. We are proposing similar
provisions here. Specifically, we are
proposing to allow foreign refiners to
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generate early credits and to apply for
temporary hardship relief and small
refiner status. See proposed 40 CFR
80.1420. However, under the earlier
rules, few foreign refiners have chosen
to undertake these additional
requirements, and almost all gasoline
produced at foreign refineries is
included in an importer’s compliance
determination for the current EPA
gasoline programs.270 We invite
comment on the value of extending
these provisions to this proposed
benzene program.
As mentioned, we are proposing to
extend the small refiner provisions to
foreign refiners. Our experience in past
rules is that they are not taken
advantage of for various reasons. Most
foreign refineries are state-owned or
owned by large multinational
companies, and would exceed the
employee-count criterion. Others have
typically not been interested in fulfilling
the enforcement-related requirements
that apply to foreign refineries. We
request comment on extending the small
refiner provisions to foreign refiners.
c. What Gasoline Would Be Subject to
the Proposed Benzene Standards?
All finished gasoline produced by a
refinery or imported by an importer
would be subject to the proposed
benzene content standard. In addition,
gasoline blending stock which becomes
finished gasoline solely upon the
addition of oxygenate would also be
subject to the proposed standard.271
Other gasoline blendstocks which are
shifted among refiners prior to turning
them into finished gasoline would not
be subject to the benzene standard. They
would be included at the point they are
converted or blended to produce
finished gasoline.
We are proposing to exclude gasoline
produced or imported for use in
California from this benzene
requirement. Although California’s
benzene averaging standard is greater
than 0.62 vol%, California in-use
benzene levels are currently below the
level of the proposed standard.272 We
270 Often, the importer of record is the foreign
reiner. In these instances, the importer/foreign
refiner has simply opted to achieve compliance via
the applicable importer provisions.
271 As stated earlier, both blending stock and
oxygenate would be included in the refinery’s or
importer’s compliance determination. Conventional
gasoline refiners are required to have agreements
with downstream oxygenate blenders to ensure that
the appropriate type and amount of oxygenate is
added to the gasoline blending stock, per 40 CFR
80.10(d). Absent such agreements, the refinery may
only include the gasoline blending stock in its
compliance determination and the oxygenate is not
included in any compliance determination.
272 California Code of Regulations, Title 13
Section 2262.
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expect this situation will continue.
There would be no additional benefit to
consumers of California gasoline or to
the implementation and benefits of the
proposed program by the inclusion of
gasoline used in California.
This proposal also would exclude
those specialized gasoline applications
that have been exempted from other
EPA gasoline rules, such as gasoline
used to fuel aircraft, or for sanctioned
racing events, gasoline that is exported
for sale and use outside of the U.S., and
gasoline used for research, development
or testing purposes, under certain
circumstances.
d. How Would Compliance With the
Benzene Standard Be Determined?
Compliance with the proposed
benzene standard would be on an
annual, calendar year basis, similar to
almost all other current gasoline
controls. A refiner’s or importer’s
compliance (or Compliance Benzene
Value, as used in the proposed
regulation) would be determined from
the annual average benzene content of
its gasoline (produced or imported), any
credits used for compliance purposes,
and any deficit carried over from the
previous year, and would have to be
0.62 vol% or lower, on a benzene
volume basis. The Compliance Benzene
Value would differ from the refiner’s or
importer’s actual annual average
benzene concentration because the latter
would be solely a volume weighted
average of the benzene concentrations of
the refinery’s or importer’s actual
gasoline batches.
Credits, in any amount, could be used
to achieve compliance. As mentioned,
we are also proposing to allow a deficit
to be carried forward for one year.
Under these circumstances, in the next
compliance period, the refinery or
importer would have to be in
compliance, that is, the refinery or
importer would have to, through
production or import practices, and/or
the use of credits, make up the deficit
from the previous year and be in
compliance with the proposed benzene
standard. This provision could be
especially helpful to refiners in the first
year of the program, until the
availability and need for credits was
established.
In the RFG and Anti-dumping
programs, and MSAT1, by extension,
refiners and importers generally include
oxygenate added downstream from the
refinery or the import facility in their
compliance calculations.273 Refiners
273 As a result, oxygenate blenders would not be
subject to the RFG, Anti-dumping or MSAT1
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and importers of RBOB are required to
account for the oxygenate in their own
compliance. As mentioned earlier,
refiners and importers of conventional
gasoline can include the oxygenate if
they have met the Anti-dumping
requirements for ensuring that the
amount and type of oxygenate was
indeed added. We are not proposing any
changes to these provisions for the
purposes of compliance with the
proposed benzene program. However,
average pool benzene levels are
expected to decrease as a result of
increased ethanol use due to
requirements of the Energy Policy Act of
2005, and this would affect both early
and standard credit generation, as will
be discussed below. However, we
request comment on how, if at all,
additional oxygenate use should be
considered, and perhaps limited, in
compliance determinations for the
proposed program.
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2. Averaging, Banking and Trading
Program
a. Early Credit Generation
As discussed, early credit generation
could occur as early as the averaging
period beginning June 1, 2007, through
the averaging period ending December
31, 2010, or ending December 31, 2014,
for small refiners. In order to generate
early benzene credits, a refinery would
first establish a benzene baseline which
is its average benzene concentration
over the period January 1, 2004, through
December 31, 2005. A refinery would be
eligible to generate early credits when it
reduced its annual average benzene
concentration by at least 10% compared
to its benzene baseline. Credits would
then be calculated based on the entire
reduction in benzene below the
baseline. Generation of early credits for
the first averaging period, June 1, 2007
through December 31, 2007, which is
less than a calendar year, would be
based on the average benzene level of
the gasoline produced only during this
period. Gasoline produced before June
1, 2007, would not be included in the
credit generation determination.
We are proposing to allow only
refiners (and not importers) to generate
early benzene credits because it is at the
refinery, or production level, where real
changes in the production of gasoline
can be made. Importers would simply
seek out blending streams or gasoline
with lower benzene, but would not have
to invest or take other action involving
the production of the lower benzene
gasoline. Furthermore, many importer
operations grow in volume, shrink in
regulations except for gasoline to which they add
other blendstocks in addition to the oxygenate.
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volume, come into existence and go out
of existence on a continual basis,
making it difficult to assess the
appropriateness of both the baseline and
any early credits. Thus, even though an
importer may have had regular,
consistent import activity during the
2004–2005 baseline period, we are
proposing that only refiners would be
allowed to apply for a benzene baseline,
and if approved, to generate early
benzene credits based on reductions in
future averaging period gasoline
benzene levels.
As discussed above, one of the
purposes of allowing the early
generation of benzene credits would be
to promote reductions in benzene
through refinery processing changes. We
are concerned that benzene reductions
due to increased oxygenate use would
result in reduced benzene
concentrations. Oxygenate use (in the
form of ethanol) in CG is expected to
increase as a result of the Energy Policy
Act requirements.274 This additional
oxygenate will dilute gasoline benzene
levels as well as extend the gasoline
pool. As a result, refinery average
benzene levels would be likely to be
lower during the early credit generation
period than during the benzene baseline
period (2004–2005) if there is an
increase in the amount of CG refiners
send for downstream blending with
ethanol (CBOB). We are concerned that
reductions in fuel benzene levels due to
oxygenate addition significantly beyond
the average levels of recent years could
result in windfall early credit generation
for some refineries. We request
comment on the likelihood of windfall
early credit generation, and if such a
situation were to occur, whether it
would warrant limiting early benzene
credits by consideration of the average
oxygenate use during the baseline
period compared to the early credit
generation period or by adjusting the
early credit trigger point. We believe
this would be less of an issue during the
standard credit generation period
beginning in 2011 (2015 for small
refiners) because of the more stringent
requirements for generating standard
credits (getting below the 0.62 vol%
standard) compared to the early credit
generation requirements (achieving a
minimum 10% reduction in baseline
benzene levels).
274 Even
though the Energy Policy Act of 2005
eliminated the oxygen mandate for RFG, oxygenate
use (in the form of ethanol) in RFG is expected to
continue.
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b. How Would Refinery Benzene
Baselines Be Determined?
As mentioned above, a refiner would
submit a benzene baseline application
to EPA for any of its refineries which
planned to generate early credits. The
benzene baseline would be the volumeweighted average of the benzene levels
of the gasoline produced by the refinery
during 2004–2005. Note that the
gasoline would be the combination of
the refinery’s RFG and CG, if applicable,
and would exclude California gasoline
and other fuels exempted from the
proposed standard. The benzene values
used in the benzene baseline calculation
should be the same as used in the RFG,
Anti-dumping and MSAT1 compliance
determinations. We are not proposing
provisions for adjusting these benzene
baselines based on circumstances
during the baseline years or otherwise.
Though we expect that most refineries
that apply for a benzene baseline would
have data for both 2004 and 2005, if a
refinery was shut down for part of the
2004–2005 period, it could still be able
to establish a benzene baseline. Under
these circumstances, the refiner would
have to provide and justify, using
refinery and engineering analyses, an
appropriate adjusted value that reflects
the likely average benzene
concentration for the refinery, had it
been fully operational. A refinery that
was non-operational for the entire
period January 1, 2004 through
December 31, 2005 would not be able to
establish a benzene baseline and
therefore not allowed to generate early
credits.
c. Credit Generation Beginning in 2011
Credits could be generated in any
annual averaging period beginning
January 1, 2011, or for small refiners,
beginning January 1, 2015. These
credits, also called standard benzene
credits, could be generated by a refinery
or importer when the refinery’s or
importer’s annual average benzene
concentration was less than the
proposed standard of 0.62 vol%.
While the proposed benzene standard
is a 49-state standard due to the fact that
California would maintain its existing
benzene standard, we request comment
on the appropriateness of allowing
California refineries to generate credits
that could be used to demonstrate
compliance outside of California.
d. How Would Credits Be Used?
We are proposing that all gasoline
benzene credits that are properly
created may be used equally and
interchangeably. That is, once
generated, there would be no difference
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between early credits and standard
credits, except for their credit life, as
discussed below. Under this proposal,
credits could be transferred to another
refiner or importer, or they could be
banked by the refinery or importer that
created them for use or transfer in a later
compliance period.
As in past credit programs, we are
proposing some limits on credit use.
First, we are proposing to limit the
number of times a credit could be
transferred. At the end of the allowable
number of transfers, the credit would
have to be used by the last transferee
before its expiration date. Second, we
are proposing that credits would have a
finite life whether or not transferred. We
are proposing that early credits, those
generated prior to 2011, would have a
three-year credit life from the start of the
program in 2011. These credits would
have to be used to achieve compliance
with the proposed benzene standard in
2011, 2012, and/or 2013, or they would
expire. In addition, we are proposing
that credits generated in 2011 and
beyond (or early credits generated by
small refiners during this period) would
have to be used within five years of the
year in which they were generated. We
had considered requiring credits be
used in order of their generation date,
that is, credits generated earlier would
have to be used before credits generated
later. However, the finite credit life is
likely to ensure this usage, and thus we
are not proposing to regulate credit use
in this manner. We are also proposing
that credit life could be extended by two
years for any credits that are generated
by or traded to approved small refiners.
Under the proposed regulations, a
refiner or importer would have to use all
benzene credits in its possession before
being allowed to have deficit carryover,
and would have to meet its own
compliance requirement before
transferring any gasoline benzene
credits. In the case of invalid credits, or
credits improperly created, all parties
would have to adjust their credit
records, reports, and compliance
calculations to reflect proper credit use.
The transferor would first correct its
own records and ensure its own
compliance, and then apply any
remaining properly created credits to
the transferee before trading or banking
those credits. See section X.A below for
more discussion of these issues.
3. Hardship and Small Refiner
Provisions
a. Hardship
The hardship provisions and
requirements are extensively discussed
in section VII.E.2, and thus are only
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briefly addressed here. We are
proposing that a refiner for any of its
refineries could seek temporary relief
from meeting the proposed benzene
standard due to unusual circumstances,
including those situations, such as a
natural disaster, which would clearly be
outside the control of the refiner. A
refiner would have to apply to EPA for
this temporary relief, and EPA could
deny the application or approve it for an
appropriate period of time. However,
given the existence of a flexible ABT
program, EPA expects that, prior to
requesting hardship relief, the refiner
would have made best efforts to obtain
credits in order to comply with the
proposed benzene standard. In past
rulemakings, for example the gasoline
sulfur rule, the hurdle for receiving a
hardship was very high, with very few
granted. While we are proposing these
provisions again here, the expectation is
that the hurdle would be even higher.
Given the existence and flexibility
afforded by the ABT program and the
more limited cost of the benzene
standard, it is our expectation that as
long as a viable credit market existed, it
would be difficult to justify granting a
hardship. Furthermore, the form of any
relief we are proposing is in the form of
additional time to demonstrate
compliance via credits as opposed to
any waiver of the standards.
b. Small Refiners
As discussed earlier, we are proposing
to allow small refiners to meet the
proposed benzene standard beginning
with the 2015 averaging period, which
is four years later than non-small
refiners and importers. Small refiners
could also generate both early and
standard credits if they can meet the
requirements of those programs. A
refiner would have to apply to EPA by
December 31, 2007 in order to be
considered a small refiner under this
proposed rule even if the entity was or
had been considered a small refiner
under other EPA rules. The
requirements for small refiners under
this rule are detailed in section VII.E.
4. Administrative and Enforcement
Related Provisions
a. Sampling/Testing
As under the Tier 2 program where a
sulfur concentration must be
determined for every batch of gasoline,
we are proposing that a benzene
concentration value also be determined
for every batch of gasoline produced or
imported. Thus, as gasoline samples are
taken for sulfur measurement, they
would also be taken for benzene
measurement. The RFG program, which
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has both a toxics emissions requirement
and a per-gallon benzene cap, already
requires a benzene value to be
determined for every batch of gasoline.
The Anti-dumping program, which has
only a toxics emissions requirement,
allows benzene values to be determined
from composite samples. See 40 CFR
80.101(i). Thus, the proposed sampling
requirement would be a change from the
current sampling methodology allowed
under the Anti-dumping provisions but
makes it consistent with the ongoing
Tier 2 sulfur program. However, unlike
the gasoline sulfur requirements, this
every batch testing requirement for
conventional gasoline benzene would
not have to occur prior to the batch
leaving the refinery. Additionally, the
batch numbering system would be the
same as that used for conventional
gasoline sulfur.
We are not proposing any changes to
the benzene test methodology. See 40
CFR 80.46(e). We are proposing sample
retention requirements similar to those
in the gasoline sulfur provisions. See 40
CFR 80.335.
b. Recordkeeping/Reporting
We are proposing to require that
records be kept for each averaging
period in order to accommodate the
proposed benzene standard and the
accompanying credit trading program.
These records would include: the
benzene baseline calculation, if
applicable; the number of early credits
generated, if applicable; the actual
average benzene concentration of
gasoline produced or imported; the
compliance benzene value; any deficit;
the number of credits generated; and
records of any credit transfers to or from
the refinery or importer, including price
of the credits and dates of transactions.
All of this information, and any other
information that EPA may require, such
as information similar to that proposed
below for inclusion in the precompliance reports, would be submitted
in a refiner’s or importer’s annual report
to the Agency. Since we are proposing
that the regulatory provisions for the
benzene control program would become
the single regulatory mechanism
covering RFG and Anti-dumping annual
average toxics requirements once the
benzene standard is in effect, and would
replace the MSAT1 requirements, we
expect to be able to streamline several
of the current reporting forms once the
proposed program is fully implemented
in 2015.
As mentioned, we are also proposing
to require that refiners and importers
submit pre-compliance reports in order
to provide information as to the likely
number of benzene credits needed and
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available, and how the refiner or
importer plans to achieve compliance
with the proposed benzene
requirements. These reports would be
required annually each June 1 from
2001 through 2011 (or through 2015 for
small refiners). In addition to
information regarding gasoline
production and the number of credits
expected to be used or produced, the
pre-compliance reports would include
information regarding the benzene
reduction technology expected to be
used, any capital commitments, and
information on the progress of the
installation of the technology. We are
also proposing that these reports
include price and quantity information
for any credits bought or sold. The
reports would include updates from the
previous year’s estimates, and
comparison of previous year actual
production to the projected values.
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c. Attest Engagements, Violations,
Penalties
We are proposing to require attest
engagements for generation of both early
and other credits, credit use, and
compliance with the proposed program,
using the usual procedures for attest
engagements. The violation and penalty
provisions applicable to this proposed
benzene program would be very similar
to the provisions currently in effect in
other gasoline programs. We request
comment on the need for additional
attest engagement, violation or penalty
provisions specific to the proposed
benzene program.
5. How Would Compliance With the
Provisions of the Proposed Benzene
Program Affect Compliance With Other
Gasoline Toxics Programs?
As discussed above, we expect that
virtually all refineries will reduce
benzene from their current levels, and
no refineries will increase it. This
impact on benzene levels, combined
with the pre-existing gasoline controls
in sulfur, RVP, and VOC performance,
means that compliance with the
benzene content provisions is also
expected to lead to compliance with the
annual average requirements on
benzene and toxics performance for
reformulated gasoline and the annual
average Anti-dumping toxics
performance for conventional gasoline.
EPA is therefore proposing that upon
full implementation in 2011 the
regulatory provisions for the benzene
control program would become the
single regulatory mechanism used to
implement these RFG and Antidumping annual average toxics
requirements, replacing the current RFG
and Anti-dumping annual average
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toxics standards as unnecessary. The
proposed benzene control program
would also replace the MSAT1
requirements. However, we propose the
RFG per gallon benzene cap of 1.3 vol%
remain in effect; we are requesting
comment on the need to retain this
requirement for RFG. Note that
compliance with the proposed benzene
standard would ensure compliance with
the aforementioned RFG, Anti-dumping
and MSAT1 requirements beginning
with the 2011 averaging period, or the
2015 averaging period for small refiners.
Thus, during the early credit generation
period, 2007 through 2010, all entities
would still be required to comply with
their applicable RFG, Anti-dumping and
MSAT1 requirements. In addition, from
2011 through 2014, small refiners would
have to continue to meet their
applicable RFG, Anti-dumping and
MSAT1 requirements. As discussed
earlier in section VII.E.2, we are also
requesting comment on the option of
allowing some refineries to meet the
proposed benzene standard early, thus
replacing the current RFG and Antidumping annual average toxics
provisions and replacing MSAT1
requirements for these refineries.
VIII. Gas Cans
Gas cans are consumer products
people use to refuel a wide variety of
gasoline-powered equipment. Their
most frequent use is for refueling lawn
and garden equipment such as lawn
mowers, trimmers, and chainsaws. They
are also routinely used for recreational
equipment such as all-terrain vehicles
and snowmobiles, and for passenger
vehicles which have run out of gas. The
gas cans are red, per ASTM
specifications, and about 95 percent of
them are made of plastic (high density
polyethelene (HDPE)). There are
approximately 20 million gas cans sold
annually and about 80 million cans are
in use nationwide. The average lifetime
of a gas can is about 5 years.
California has established an
emissions control program for gas cans
which began in 2001. Since then, some
other states have adopted the California
requirements. Last year, California
adopted a revised program which is
very similar to the one we are proposing
in this rulemaking. Manufacturers are
required to meet the new requirements
in California by July 1, 2007 at the
latest. State programs are discussed
further in section VIII.A.3., below.
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A. Why Are We Proposing an Emissions
Control Program for Gas Cans?
1. VOC Emissions
We are proposing standards to control
VOCs as an ozone precursor and also to
minimize exposure to VOC-based toxics
such as benzene and toluene. Gasoline
is highly volatile and evaporates easily
from containers that are not sealed or
closed properly. Although an individual
gas can is a relatively modest emission
source, the cumulative VOC emissions
from gas cans are quite significant. We
estimate that containers currently emit
about 315,000 tons of VOC annually
nationwide, which is equal to about 5
percent of the nationwide mobile source
inventory (see section V.A.). Left
uncontrolled, a gas can’s evaporative
emissions are up to 60 times the VOC
of a new Tier 2 vehicle evaporative
control system. Gas can emissions are
primarily of three types: evaporative
emissions from unsealed or open
containers; permeation emissions from
gasoline passing through the walls of
the plastic containers; and evaporative
emissions from gasoline spillage during
use.
As discussed in section IV. above,
ozone continues to be a significant air
quality concern, and gas cans are
currently an uncontrolled source of
VOC emissions in many areas of the
country. Section 183(e) of the Clean Air
Act directs EPA to study, list, and
regulate consumer and commercial
products that are significant sources of
VOC emissions. In 1995, after
conducting a study and submitting a
Report to Congress on VOC emissions
from consumer and commercial
products, EPA published an initial list
of product categories to be regulated
under section 183(e). Based on criteria
that we established pursuant to section
183(e)(2)(B), we listed for regulation
those consumer and commercial
products that we considered at the time
to be significant contributors to the
ozone nonattainment problem, but we
did not include gas can emissions.275
After analyzing the emissions inventory
impacts of gas cans, EPA plans to
publish a Federal Register notice that
would add portable gasoline containers
to the list of consumer products to be
regulated and explain the rationale for
this action in detail. EPA will afford
interested persons the opportunity to
comment on the data underlying the
listing before taking final action on
today’s proposal. In today’s notice, EPA
is proposing that the standards for
275 60 FR 15264 ‘‘Consumer and Commercial
Products: Schedule for Regulation,’’ March 23,
1995.
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portable gasoline containers represent
‘‘best available controls’’ as required by
section 183(e)(3)(A). Determination of
the ‘‘best available controls’’ requires
EPA to determine the degree of
reduction achievable through use of the
most effective control measures (which
includes chemical reformulation, and
other measures) after considering
technological and economic feasibility,
as well as health, energy, and
environmental impacts.276
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2. Technological Opportunities to
Reduce Emissions From Gas Cans
Gas can manufacturers have already
developed and applied emissions
controls in response to California
requirements. Traditional gas cans
typically have a spout for pouring fuel
and a vent at the rear of the can to allow
air to flow into the cans when in use.
About 70 percent of emissions from gas
cans are due to evaporative losses from
caps being left off one or both of these
openings. The primary way to reduce
these emissions is to design cans that
are not easily left open. To accomplish
this, gas can manufacturers have
developed spouts that incorporate a
spring mechanism to close cans
automatically when not in use. Many
spout designs are opened by consumers
pushing the spout against the
equipment fuel tank. Some designs
incorporate a button or trigger
mechanism that the consumer pushes to
start fuel flow and then releases when
done refueling. Also, some cans are
made without rear vents, incorporating
venting into the spouts and thus
eliminating one potential emission
point. The consumer still must remove
the spout to refill the cans but would
replace the spout once the can is full in
order to prevent spillage during
transport.
The auto-closing spouts reduce
spillage by giving consumers greater
control over the fuel flow. The spouts
allow consumers to place the can in
position before activating or opening the
cans. Once the receiving fuel tank is
full, consumers can easily release the
mechanism to stop the fuel flow. This
reduces spillage during the positioning
and removal of the can and reduces
overall spillage by about half.
Consumers generally appreciate the
greater control over the refueling event.
Blow-molding is used to manufacture
gas cans. Typically, blow-molding is
performed by creating a hollow tube,
known as a parison, by pushing high276 See section 183(e)(1); see also section 183(e)(4)
providing broad authority to include ‘‘systems of
regulation’’ in controlling VOC emissions from
consumer products.
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density polyethylene (HDPE) through an
extruder with a screw. The parison is
then pinched in a mold and inflated
with an inert gas. The HDPE plastics
used for gas cans allow gasoline
molecules to permeate (i.e., pass
through) the walls of the container. This
contributes to overall emission losses
from the containers. There are several
effective permeation barriers that can be
incorporated into the can walls. Gas can
manufacturers have used several of
these methods to meet California
program requirements. The technologies
were initially developed to meet
automotive evaporative emissions
standards and are now also being used
for other types of fuel tanks. The
barriers are either incorporated as part
of the manufacturing process of the can
(either as a layer or by mixing the
barrier materials with the plastics) or are
applied to the cans after they are
manufactured. These barriers typically
achieve reductions of 85 percent or
better compared to untreated cans.
Some gas can manufacturers have
produced non-permeable plastic gas
cans by blow molding a layer of
ethylene vinyl alcohol (EVOH) or nylon
between two layers of polyethylene.
This process is called coextrusion and
requires at least five layers: The barrier
layer, adhesive layers on either side of
the barrier layer, and HDPE as the
outside layers which make up most of
the thickness of the gas can walls.
However, this blow-molding process
requires two additional extruder screws,
which significantly increases its cost.
An alternative to coextrusion is to
blend a low-permeability resin with the
HDPE and extrude it with a single screw
to create barrier platelets. The trade
name typically used for this permeation
control strategy is Selar. The lowpermeability resin, typically EVOH or
nylon, creates non-continuous platelets
in the HDPE gas can which reduce
permeation by creating long, tortuous
pathways that the hydrocarbon
molecules must navigate to pass through
the gas can walls. Although the barrier
is not continuous, this strategy can still
achieve greater than a 90-percent
reduction in permeation of gasoline.
EVOH has much higher permeation
resistance to alcohol than nylon;
therefore, it would be the preferred
material to use for meeting our proposed
standard (described at Section B.,
below), which is based on testing with
a 10-percent ethanol fuel.
Another type of low permeation
technology for HDPE gas cans is treating
the surfaces of plastic gas cans with a
barrier layer. Two ways of achieving
this are known as fluorination and
sulfonation. The fluorination process
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causes a chemical reaction where
exposed hydrogen atoms are replaced by
larger fluorine atoms, creating a barrier
on the surface of the gas can. In this
process, a batch of gas cans is generally
processed post production by stacking
them in a steel container. The container
is then voided of air and flooded with
fluorine gas. By pulling a vacuum in the
container, the fluorine gas is forced into
every crevice in the gas can. As a result
of this process, both the inside and
outside surfaces of the gas can would be
treated. As an alternative, gas cans can
be fluorinated on the manufacturing line
by exposing the inside surface of the gas
can to fluorine during the blow molding
process. However, this method may not
prove as effective as off-line
fluorination, which treats the inside and
outside surfaces.
Sulfonation is another surface
treatment technology. In this process,
sulfur trioxide reacts with the exposed
polyethylene to form sulfonic acid
groups on the surface. Current practices
for sulfonation are to place a gas can on
a small assembly line and expose the
inner surfaces to sulfur trioxide, then
rinse with a neutralizing agent.
However, sulfonation can also be
performed using a batch method. Either
of these processes can be used to reduce
gasoline permeation by more than 95
percent.
3. State Experiences Regulating Gas
Cans
California established an emissions
control program for gas cans that began
in 2001.277 Twelve other states and the
District of Columbia have adopted the
California program in recent years.
These states include Delaware, Maine,
Maryland, Pennsylvania, New York,
Connecticut, Massachusetts, New Jersey,
Rhode Island, Vermont, Virginia,
Washington, DC, and Texas.
Last year, California adopted a revised
program that is very similar to the one
we are proposing in this rulemaking.278
California’s new program goes into
effect on July 1, 2007. California
addressed several deficiencies they
observed in their first program by
adding new enhanced diurnal
standards, new testing requirements,
and new certification requirements, and
by removing automatic shut-off
requirements that lead to designs that
do not work well in the field.
277 Portable Fuel Container Spillage Control
Regulations, Final Statement of Reasons, State of
California Environmental Protection Agency Air
Resources Board, June 2000.
278 Public Hearing to Consider Amendments to
the Regulations for Portable Fuel Containers, Final
Statement of Reasons, California Air Resources
Board, October 2005.
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California’s original program contained
several design specifications which
limited manufacturer flexibility and
resulted, in many cases, in products that
were difficult for consumers to use.
California has removed most of these
design specifications from their revised
program.
California’s original program included
an automatic shut-off requirement
intended to reduce spillage caused by
overfilling the receiving fuel tank. The
spouts were required to be designed to
stop fuel flow when the fuel reached the
tip of the spout, similar to how gas
pumps shut off when refueling a
vehicle. California specified a test
fixture, the height of the fuel in the
receiving tank at which point the fuel
flow must stop, and the minimum fuel
flow rate. The gas cans were designed
by manufacturers to work well with the
test fixture, but the automatic shut-off
failed in use a significant amount of the
time. California found that the design of
the equipment fuel tank had a big
impact on the performance of the
automatic shut-off. Due to the wide
variety of fuel tank designs, the
automatic shut-off worked on a
relatively small percentage of
equipment. In addition, many of the
spout designs were not compatible with
passenger vehicles. This is especially
critical because the cans are customarily
used by consumers when their vehicles
run out of gas.
These problems led to many
consumer complaints to both the
manufacturers and to the California Air
Resources Board. It also led to increased
spillage in many cases. It was also found
that many consumers did not
understand how the spouts were
supposed to operate. Even in cases
where the spouts would have stopped
the flow of fuel in time, consumers did
not use the cans properly. Consumers
are used to actively controlling the flow
of fuel. For these reasons, California
removed the automatic shut-off
requirements from their program for all
cans.
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B. What Emissions Standard Is EPA
Proposing, and Why?
1. Description of Emissions Standard
We are proposing a performancebased standard of 0.3 grams per gallon
per day (g/gal/day) of HC to control
evaporative and permeation losses. The
standard would be measured based on
the emissions from the can over a
diurnal test cycle. The cans would be
tested as a system with their spouts
attached. Manufacturers would test the
cans by placing them in an
environmental chamber which
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simulates summertime ambient
temperature conditions and cycling the
cans through the 24-hour temperature
profile (72–96° F), as discussed below.
The test procedures, which are
described in more detail below, would
ensure that gas cans meet the emission
standard over a range of in-use
conditions such as different
temperatures, different fuels, and taking
into consideration factors affecting
durability.
2. Determination of Best Available
Control
The 0.3 g/gal/day emissions standard
and associated test procedures reflect
the performance of the best available
control technologies discussed above,
including durable permeation barriers,
auto-closing spouts, and a can that is
well-sealed to reduce evaporative losses.
The standard is both economically and
technologically feasible. As discussed
above, to comply with California’s
program, gas can manufacturers have
developed gas cans with low VOC
emissions at a reasonable cost (see
section IX. for costs). Testing of cans
designed to meet CARB standards has
shown the proposed standards to be
technologically feasible. When tested
over cycles very similar to those we are
proposing, emissions from these cans
have been in the range of 0.2–0.3 g/gal/
day.279 These cans have been produced
with permeation barriers representing a
high level of control (over 90 percent
reductions) and with auto-closing
spouts, which are technologies that
represent best available controls for gas
cans. Establishing the standard at 0.3 g/
gal/day would require the use of best
available technologies. We are
proposing a level at the upper end of the
tested performance range to account for
product performance variability. In
addition, we believe that any of the
current best designs can achieve these
levels, so we do not believe that the
proposed standard forecloses use of any
of the existing performing product
designs. Our detailed feasibility analysis
is provided in the Regulatory Impact
Analysis. We request comment on the
level of the standard and on its
feasibility. We request that commenters
provide detail and data where possible.
In addition to considering
technological and economic feasibility,
section 183(e)(1)(A) requires us to
consider ‘‘health, environmental, and
energy impacts’’ in assessing best
available controls. Environmental and
279 ‘‘Quantification of Permeation and
Evaporative Emissions From Portable Fuel
Container’’, California Air Resources Board, June
2004.
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health impacts are discussed in section
IV. Moreover, control of spillage from
gas cans may reduce fire hazards as well
because cans would stay tightly closed
if tipped over. We expect the energy
impacts of gas can control to be positive,
because the standards will reduce
evaporative fuel losses.
3. Emissions Performance vs. Design
Standard
We are proposing an emissions
performance standard rather than
mandating that gas cans be of any
specified design. Rather than proposing
to require that gas cans only have one
opening, or other design-based
requirements, we believe that it is
sufficient to require gas cans to meet an
emissions performance standard. A
performance standard allows flexibility
in can design while ensuring the overall
emissions performance of the cans. We
are reluctant to specify design standards
for consumer products in order not to
limit manufacturer (and ultimately
consumer) choice. The market will
encourage manufacturers to offer
products that work well for consumers,
and design-based requirements could
unnecessarily limit manufacturer design
flexibility.
4. Automatic Shut-Off
We are not requiring automatic shutoff as a design-based standard, or
considering it to be a ‘‘best available
control.’’ As described in section
VIII.A.3. above, the automatic shut-off
has been shown to be problematic for
consumers for several reasons, and we
believe that including requirements for
automatic shut-off would be
counterproductive. Automatic shut-off
is supposed to stop the flow of fuel
when the fuel reaches the top of the
receiving tank in order to prevent overfilling. However, due to a wide variety
of receiving fuel tank designs, the auto
shut off spouts do not work well with
a variety of equipment types. In
California, this problem led to spillage
and consumer dissatisfaction. We want
to avoid cases where spills occur even
when consumers are using the products
properly due to a mismatch between the
spout design and the design of the
receiving fuel tank being filled.
Excessive consumer difficulties in using
new cans would likely lead to some
consumers defeating the low emissions
features of the cans by removing the
spouts and using other means such as
funnels to refuel equipment. Any
additional emissions reductions
provided by automatic shut-off in cases
where it worked properly would likely
be largely or completely offset by
increased spillage due to cases where
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consumers defeated the designs or the
designs failed to work properly. We
believe that the automatic closing cans,
even without automatic shut-off
requirements, will lead to reduced
spillage. As discussed above, automatic
closure keeps the cans closed when they
are not in use and provides more control
to the consumer during use.
Some additional reduction in spillage
is likely possible in some cases with
automatic shut-off, but may not be
feasible across the wide array of gas can
usage. It is possible to design a spout
that works well on some equipment but
not for all equipment. It might also be
possible to cover more uses by having
multiple spouts, but we believe that
having multiple spouts would lead to
confusion and would also require
consumers to have multiple cans
depending on the types of equipment
that they refuel. We request comment on
automatic shut-off requirements and on
ways to establish an automatic shut-off
requirement that would reduce spillage,
be feasible for manufacturers, and be
practical for consumers.
5. Consideration of Retrofits of Existing
Gas Cans
Clean Air Act section 183(e) provides
authority to consider retrofitting
gasoline containers as an approach for
controlling emissions. We do not
believe, however, that requiring the
retrofit of existing gas cans would be a
feasible approach for controlling gas can
emissions, either technically or
economically. This would likely entail
manufacturers first developing retrofit
systems (including spouts for various
previous gas can designs), testing them
for emissions performance, and
certifying them with EPA.
Manufacturers would need time to
develop and certify systems and also to
develop an implementation strategy,
considering that there are millions of
cans in use. Manufacturers would then
likely need to collect gas cans from
consumers, recondition the cans,
permanently close vents, incorporate
permeation barriers, and incorporate
new spouts. We believe that this process
would lead to costs that far exceed the
cost of newly manufactured gas cans. In
addition, emissions reductions would
depend on consumer participation,
which would be highly uncertain given
that gas cans are relatively low-cost
consumer products. In fact, we believe
that consumers who are concerned
about emissions would be more likely to
discard old gas cans and purchase new
cans meeting emissions standards. For
all these reasons, we do not believe that
a retrofitting approach makes sense for
gas cans.
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6. Consideration of Diesel, Kerosene and
Utility Containers
We are requesting comment on but
not proposing applying emissions
control requirements to diesel, kerosene,
and utility containers. Due to the low
volatility of diesel and kerosene, the
evaporative losses from diesel and
kerosene cans would be minimal when
used with the designated fuels.
California has included diesel and
kerosene cans in their regulations
largely due to the concern that they
would be purchased as substitutes for
gasoline containers. California also
included utility containers in their
portable fuel container program due to
concerns that these containers would be
used for gasoline. We believe that
manufacturers can minimize this
incentive by designing gasoline cans
and spouts that are easy to use and
beneficial to the consumer. However,
storing gasoline in diesel, kerosene, and
utility containers would result in a loss
of emissions reductions and therefore
we are requesting comment on
including them in the program. The
costs for these containers would be
similar to the costs estimated for
gasoline containers. We request
comment on the potential for diesel,
kerosene, and utility containers to be
used as a substitute for regulated gas
cans, and the cost and other
implications of including them in the
program.
C. Timing of Standard
As an aspect of considering the
proposed standard’s technological
feasibility, we are proposing to require
manufacturers to meet the standard
beginning January 1, 2009.
Manufacturers have developed the
primary technologies to reduce
emissions from gas cans but will need
a few years of lead time to certify
products and ramp up production to a
national scale. The certification process
would take at least six months due to
the required durability demonstrations
described below, and manufacturers
would need time to procure and install
the tooling needed to produce gas cans
with permeation barriers for nationwide
sales.
The standards would apply to gas
cans manufactured on or after the start
date of the program and would not
affect cans produced before the start
date. We propose that as of July 1, 2009,
manufacturers and importers must not
enter into U.S. commerce any products
not meeting the emissions standards.
This provides manufacturers with a 6month period to clear any stocks of gas
cans manufactured prior to the January
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1, 2009 start of the program, allowing
the normal sell through of these cans to
the retail level. Retailers would be able
to sell their stocks of gas cans through
the course of normal business without
restriction. Gas cans are currently
stamped with their production date,
which would allow EPA to determine
which cans are required to meet the new
standards.
We believe that the 2009 time frame
is feasible, but recognize that it could be
a challenge for manufacturers with high
volume sales to ramp up production.
We request comment on the economic
feasibility of the proposed timing and
also on whether or not a phase-in of the
standards would ease the transition to a
national program. We encourage
commenters to provide detailed
rationale and data where possible to
support their comments.
D. What Test Procedures Would Be
Used?
As part of the proposed system of
regulations for gas cans, we are
proposing test conditions designed to
assure that the intended emission
reductions occur over a range of in-use
conditions such as operating at different
temperatures, with different fuels, and
considering factors affecting durability.
These proposed test procedures
implement section 183(e)(4), which
authorizes EPA to develop appropriate
standards relating to product use.
Emission testing on all gas cans that
manufacturers produce is not feasible
due to the high volumes of gas cans
produced every year and the cost and
time involved with emissions testing.
Instead, we are proposing that before the
gas cans are introduced into commerce,
EPA would need to certify gas cans to
the emissions standards based on
manufacturers’ applications for
certification. Manufacturers would
submit test data on a sample of gas cans
that are prototypes of the products
manufacturers intend to produce.
Manufacturers would also need to
certify that their production cans would
not deviate in materials or design from
the prototype gas cans that are tested.
Manufacturers would need to obtain
approval of their certification from EPA
prior to introducing their products into
commerce. The proposed test
procedures and certification
requirements are described in detail
below.
We are proposing that manufacturers
would test cans in their most likely
storage configuration. The key to
reducing evaporative losses from gas
cans is to ensure that there are no
openings on the cans that could be left
open by the consumer. Traditional cans
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have vent caps and spout caps that are
easily lost or left off cans, which leads
to very high evaporative emissions. We
expect manufacturers to meet the
evaporative standards by using
automatic closing spouts and by
removing other openings that
consumers could leave open. However,
if manufacturers choose to design cans
with an opening that does not close
automatically, we are proposing to
require that containers be tested in their
open condition. If the gas cans have any
openings that consumers could leave
open (for example, vents with caps),
these openings thus would need to be
left open during testing. This would
apply to any opening other than where
the spout attaches to the can. We believe
it is important to take this approach
because these openings could be a
significant source of in-use emissions
and there is a realistic possibility that
these openings would be inadvertently
left open in use.
We propose that spouts would be in
place during testing because this would
be the most likely storage configuration
for the emissions compliant cans.
Spouts would still be removable so that
consumers would be able to refill the
cans, but we would expect the
containers to be resealed by consumers
after being refilled in order to prevent
spillage during transport. We do not
believe that consumers would routinely
leave spouts off cans because spouts are
integral to the cans’ use and it is
obvious that they need to be sealed.
1. Diurnal Test
We are proposing a test procedure for
diurnal emissions testing where
manufacturers (or others conducting the
testing) place gas cans in an
environmental chamber or a Sealed
Housing for Evaporative Determination
(SHED), vary the temperature over a
prescribed temperature and time profile,
and measure the hydrocarbons escaping
from the gas can. We are proposing that
gas cans would be tested over the same
72–96 °F (22.2–35.6 °C) temperature
profile used for automotive
applications. This temperature profile
represents a hot summer day when
ground level ozone emissions (formed
from hydrocarbons and oxides of
nitrogen) would be highest. We propose
that three containers would be tested,
each over a three-day test. We are
proposing that three cans would be
tested for certification in order to
address variability in products or test
measurements. All three cans would
have to individually meet the proposed
standard. As noted above, gas cans
would be tested in their most likely
storage configuration.
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The final result would be reported in
grams per gallon, where the grams are
the mass of hydrocarbons escaping from
the gas can over 24 hours and the
gallons are the nominal gas can
capacity. The daily emissions would
then be averaged for each can to
demonstrate compliance with the
standard. This test would capture
hydrocarbons lost through permeation
and any other evaporative losses from
the gas can as a whole. We are
proposing that the grams of
hydrocarbons lost would be determined
by either weighing the gas can before
and after the diurnal test cycle or
measuring emissions directly using the
SHED instrumentation.
Consistent with the automotive test
procedures, we are proposing that the
testing take place using 9 pounds per
square inch (psi) Reid Vapor Pressure
(RVP) certification gasoline, which is
the same fuel required by EPA to be
used in its other evaporative test
programs. We are proposing for this
testing to use E10 fuel (10% ethanol
blended with the gasoline described
above) in this testing to help ensure inuse emission reductions on ethanolgasoline blends, which tend to have
increased evaporative emissions with
certain permeation barrier materials. We
believe including ethanol in the test fuel
will lead to the selection of materials by
manufacturers that are consistent with
‘‘best available control’’ requirements
for all likely contained gasolines, and is
clearly appropriate given the expected
increase over time of the use of ethanol
blends of gasoline under the renewable
fuel provisions of the Energy Policy Act
of 2005. Diurnal emissions are not only
a function of temperature and fuel
volatility, but of the size of the vapor
space in the container as well. We are
proposing that the fill level at the start
of the test be 50% of the nominal
capacity of the gas can. This would
likely be the average fuel level of the gas
can in-use. Nominal capacity of the gas
cans would be defined as the volume of
fuel, specified by the manufacturer, to
which the gas can could be filled when
sitting on level ground. The vapor space
that normally occurs in a gas can, even
when ‘‘full,’’ would not be considered
in the nominal capacity of the gas can.
All of these test requirements are
proposed to represent typical in-use
storage conditions for gas cans, on
which EPA can base its emissions
standards. These provisions are
proposed as a way to implement the
standards effectively, which will lead to
the use of best available technology at
a reasonable cost.
Before testing for certification, the gas
cans would be run through the
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durability tests described below. Within
8 hours of the end of the soak period
contained in the durability cycle, the
gas cans would be drained and refilled
to 50 percent nominal capacity with
fresh fuel, and then the spouts reattached. When the gas can is drained,
it would have to be immediately refilled
to prevent it from drying out. The
timing of these steps is needed to ensure
that the stabilized permeation emissions
levels are retained. The can will then be
weighed and placed in the
environmental chamber for the diurnal
test. After each diurnal, the can would
be re-weighed. In lieu of weighing the
gas cans, we propose that manufacturers
could opt to measure emissions from the
SHED directly. For any in-use testing of
gas cans, the durability procedures
would not be run prior to testing.
California’s test procedures are very
similar to those described above.
However, the California procedure
contains a more severe temperature
profile of 65–105 °F. We propose to
allow manufacturers to use this
temperature profile to test gas cans as
long as other parts of the EPA test
procedures are followed, including the
durability provisions below. We request
comment on these test procedures,
including ways the procedures may be
further streamlined without impacting
the overall emissions measurements and
performance of the gas cans.
2. Preconditioning To Ensure Durable
In-Use Control
a. Durability Cycles
To determine permeation emission
deterioration rates, we are specifying
three durability aging cycles: Slosh,
pressure-vacuum cycling, and
ultraviolet exposure. They represent
conditions that are likely to occur in-use
for gas cans, especially for those cans
used for commercial purposes and
carried on truck beds or trailers. The
purpose of these deterioration cycles is
to help ensure that the technology
chosen by manufacturers is durable inuse, representing best available control,
and the measured emissions are
representative of in-use permeation
rates. Fuel slosh, pressure cycling, and
ultraviolet (UV) exposure each impact
the durability of certain permeation
barriers, and we believe these cycles are
needed to ensure long-term emissions
control. Without these durability cycles,
manufacturers could choose to use
materials that meet the certification
standard but have degraded
performance in-use, leading to higher
emissions. We do not expect these
procedures to adversely impact the
feasibility of the standards, because
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there are permeation barriers available
at a reasonable cost that do not
deteriorate significantly under these
conditions (which permeation barriers
are examples of best available controls).
As described above, we believe
including these cycles as part of the
certification test is preferable to a
design-based requirement.
For slosh and pressure cycling, we are
proposing to use durability tests that are
based on draft recommended SAE
practice for evaluating permeation
barriers.280 For slosh testing, the gas can
would be filled to 40 percent capacity
with E10 fuel and rocked for 1 million
cycles. The pressure-vacuum testing
contains 10,000 cycles from ¥0.5 to 2.0
psi. The third durability test is intended
to assess potential impacts of ultraviolet
(UV) sunlight (0.2 µm–0.4 µm) on the
durability of a surface treatment. In this
test, the gas cans must be exposed to a
UV light of at least 0.40 Watt-hour/
meter2 /minute on the gas can surface
for 15 hours per day for 30 days.
Alternatively, gas cans could be exposed
to direct natural sunlight for an
equivalent period of time. We have also
established these same durability
requirements as part of our program to
control permeation emissions from
recreational vehicle fuel tanks.281 While
there are obvious differences in the use
of gas cans compared to the use of
recreational vehicle fuel tanks, we
believe the test procedures offer
assurance that permeation controls used
by manufacturers will be robust and
will continue to perform as intended
when in use. We request comments on
the use of these procedures for gas cans
to help ensure permeation control inuse.
We also propose to allow
manufacturers to do an engineering
evaluation, based on data from testing
on their permeation barrier, to
demonstrate that one or more of these
factors (slosh, UV exposure, and
pressure cycle) do not impact the
permeation rates of their gas cans and
therefore that the durability cycles are
not needed. Manufacturers would use
data collected previously on gas cans or
other similar containers made with the
same materials and processes to
demonstrate that the emissions
performance of the materials does not
degrade when exposed to slosh, UV,
and/or pressure cycling. The test data
280 Draft SAE Information Report J1769, ‘‘Test
Protocol for Evaluation of Long Term Permeation
Barrier Durability on Non-Metallic Fuel Tanks,’’
(Docket A–2000–01, document IV–A–24).
281 Final Rule, ‘‘Control of Emissions from
Nonroad Large Spark-ignition engines, and
Recreational Engines (Marine and Land-based)’’, 67
FR 68287, November 8, 2002.
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would have to be collected under
equivalent or more severe conditions as
those noted above.
b. Preconditioning Fuel Soak
It takes time for fuel to permeate
through the walls of containers.
Permeation emissions will increase over
time as fuel slowly permeates through
the container wall, until the permeation
finally stabilizes when the saturation
point is reached. We want to evaluate
emissions performance once permeation
emissions have stabilized, to ensure that
the emissions standard is met in-use.
Therefore, we are proposing that prior to
testing the gas cans, the cans would
need to be preconditioned by allowing
the cans to sit with fuel in them until
the hydrocarbon permeation rate has
stabilized. Under this step, the gas can
would be filled with a 10-percent
ethanol blend in gasoline (E10), sealed,
and soaked for 20 weeks at a
temperature of 28 ± 5° C. As an
alternative, we are proposing that the
fuel soak could be performed for 10
weeks at 43 ± 5°C to shorten the test
time. During this fuel soak, the gas cans
would be sealed with the spout
attached. This is representative of how
the gas cans would be stored in-use. We
have established these soak
temperatures and durations based on
protocols EPA has established to
measure permeation from fuel tanks
made of HDPE.282 These soak times
should be sufficient to achieve
stabilized permeation emission rates.
However, if a longer time period is
necessary to achieve a stabilized rate for
a given gas can, we would expect the
manufacturer to use a longer soak
period (and/or higher temperature)
consistent with good engineering
judgment.
Durability testing that is performed
with fuel in the gas can may be
considered part of the fuel soak
provided that the gas can continuously
has fuel in it. This approach would
shorten the total test time. For example,
the length of the UV and slosh tests
could be considered as part of the fuel
soak provided that the gas can is not
drained between these tests and the
beginning of the fuel soak.
c. Spout Actuation
In its recently revised program for gas
cans, California included a durability
demonstration for spouts. We are
proposing a durability demonstration
consistent with California’s procedures.
Automatically closing spouts are a key
282 Final Rule, ‘‘Control of Emissions from
Nonroad Large Spark-ignition engines, and
Recreational Engines (Marine and Land-based)’’, 67
FR 68287, November 8, 2002.
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part of the emissions controls expected
to be used to meet the proposed
standards. If these spouts stick or
deteriorate, in-use emissions could
remain very high (essentially
uncontrolled). We are interested in ways
to ensure during the certification
procedures that the spouts also remain
effective in use. California requires
manufacturers to actuate the spouts 200
times prior to the soak period and 200
times near the conclusion of the soak
period to simulate spout use. The
spouts’ internal components would be
required to be exposed to fuel by tipping
the can between each cycle. Spouts that
stick open or leak during these cycles
would be considered failed. The total of
400 spout actuations represents about
1.5 actuations per week on average over
the average container life of 5 years. In
the absence of data, we believe this
number of actuations appears to
reasonably replicate the number that
can occur in-use for high end usage and
will help ensure quality spout designs
that do not fail in-use. We also believe
that proposing requirements consistent
with California will help manufacturers
to avoid duplicate testing. We request
comment on the above approach for
demonstrating spout durability.
E. What Certification and In-Use
Compliance Provisions Is EPA
Proposing?
1. Certification
Section 183(e)(4) authorizes EPA to
adopt appropriate systems of regulations
to implement the program, including
requirements ranging from registration
and self-monitoring of products, to
prohibitions, limitations, economic
incentives and restrictions on product
use. We are proposing a certification
mechanism pursuant to these
authorities. Manufacturers would be
required to go through the certification
process specified in the proposed
regulations before entering their
containers into commerce. To certify
products, manufacturers would first
define their emission families. This is
generally based on selecting groups of
products that have similar emissions.
For example, co-extruded gas cans of
various geometries could be grouped
together. The manufacturer would select
a worst-case configuration for testing,
such as the thinnest-walled gas can.
These determinations may be made
using good engineering judgment and
would be subject to EPA review. Testing
with those products, as specified above,
would need to show compliance with
emission standards. The manufacturers
would then send us an application for
certification. We propose to define the
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manufacturer as the entity that is in dayto-day control of the manufacturing
process (either directly or through
contracts with component suppliers)
and responsible for ensuring that
components meet emissions-related
specifications. Importers would not be
considered a manufacturer and thus
would not be certifying entities; the
manufacturers of the cans they import
would have to certify the cans.
Importers would only be able to import
gas cans that are certified.
After reviewing the information in the
application, we would issue a certificate
of conformity allowing manufacturers to
introduce into commerce the gas cans
from the certified emission family. EPA
review would typically take about 90
days or less, but could be longer if we
have questions regarding the
application. The certificate of
conformity would be for a production
period of up to five years.
Manufacturers could carry over
certification test data if no changes are
made to their products that would affect
emissions performance. Changes to the
certified products that would affect
emissions would require reapplication
for certification. Manufacturers wanting
to make changes without doing testing
would be required to present an
engineering evaluation demonstrating
that emissions are not affected by the
change.
The certifying manufacturer accepts
the responsibility for meeting applicable
emission standards. While we are
proposing no requirement for
manufacturers to conduct productionline testing, we may pursue EPA in-use
testing of certified products to evaluate
compliance with emission standards. If
we find that gas cans do not meet
emissions standards in use, we would
consider the new information during
future product certification. Also, we
may require certification prior to the
end of the five-year production period
otherwise allowed between
certifications. The details of the
proposed certification process are
provided in the proposed regulatory
text. We request comments on the
certification process we are proposing.
2. Emissions Warranty and In-Use
Compliance
We are proposing a warranty period of
one year to be provided by the
manufacturer of the gas can to the
consumer. The warranty would cover
emissions-related materials defects and
breakage under normal use. For
example, the warranty would cover
failures related to the proper operation
of the auto-closing spout or defects with
the permeation barriers. We are also
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proposing to require that manufacturers
submit a warranty and defect report
documenting successful warranty
claims and the reason for the claim to
EPA annually so that EPA may monitor
the program. Unsuccessful claims
would not need to be submitted. We
believe that this warranty will
encourage designs that work well for
consumer and are durable. Although it
does not fully cover the average life of
the product, it is not typical for very
long warranties to be offered with
products and therefore we believe a one
year warranty is reasonable. Also, the
warranty period is more similar to the
expected life of gas cans when used in
commercial operations, which would
need to be considered by the
manufacturers in their designs. We
request comment on the warranty
period.
EPA views this aspect of the proposal
as another part of the ‘‘system of
regulation’’ it is proposing to control
VOC emissions from gas cans, which
system may include ‘‘requirements for
registration and labeling * * * use, or
consumption * * * of the product’’
pursuant to section 183(e)(4) the Act. A
warranty will promote the objective of
the proposed rule by assuring that
manufacturers will ‘‘stand behind’’ their
product, thus improving product design
and performance. Similarly, the
proposed defect reporting requirement
will promote product integrity by
allowing EPA to readily monitor in-use
performance by tracking successful
warranty claims.
Gas cans have a typical life of about
five years on average before they are
scrapped. We are proposing durability
provisions as part of certification testing
to help ensure containers perform well
in use (a system of regulation for ‘‘use’’
of the product, pursuant to section
183(e)(4)). Under the proposal, we could
test gas cans within their five-year
useful life period to monitor in-use
performance and take steps to correct
in-use failures, including denying
certification, for container designs that
are consistently failing to meet
emissions standards. (This proposed
provision thus would work in tandem
with the warranty claim reporting
provision proposed in the preceding
paragraph.)
We are not proposing any recall
provisions for gas cans. Manufacturers
do not have registration programs for
gas cans and implementing such a
program for a low-cost consumer
product may be overly burdensome, and
have a very low participation rate. Also,
we would not expect a high
participation rate from consumers in a
recall, in any event, due to the nature of
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gas cans as a consumer product. We
believe, however, that by having the
authority to test products in use, along
with the possible repercussions of inuse noncompliance, will encourage
manufacturers to develop robust
designs.
3. Labeling
Since the requirements will be
effective based on the date of
manufacture of the gas can, we propose
that the date of manufacture must be
indelibly marked on the can. This is
consistent with current industry
practices. This is needed so that we and
others can recognize whether a unit is
regulated or not. In addition, we
propose to require a label providing the
manufacturer name and contact
information, a statement that the can is
EPA certified, citation of EPA
regulations, and a statement that it is
warranted for one year from the date of
purchase. The manufacturer name and
contact information is necessary to
verify certification. Indicating that a 1
year warranty applies will ensure that
consumers have knowledge of the
warranty and a way to contact the
manufacturer. Enforcement of the
warranty is critical to the defect
reporting system. In proposing this
labeling requirement, we further
believe, pursuant to section 183(e)(8),
that these labeling requirements would
be useful in meeting the NAAQS for
ozone. They provide necessary means of
implementing the various measures
described above which help ensure that
VOC emission reductions from the
proposed standard will in fact occur in
use.
F. How Would State Programs Be
Affected by EPA Standards?
As described in section VIII.A.3.
above, several states have adopted
emissions control programs for gas cans.
California implemented an emissions
control program for gas cans in 2001.
Thirteen other states, mostly in the
northeast, have adopted the California
program in recent years.283 Last year,
California adopted a revised program,
which will go into effect on July 1, 2007.
The revised California program is very
similar to the program we are proposing.
We believe that although a few aspects
of the program we are proposing are
different, manufacturers will be able to
meet both EPA and CARB requirements
with the same gas can designs and
therefore sell a single product in all 50
283 Delaware, Maine, Maryland, Pennsylvania,
New York, Connecticut, Massachusetts, New Jersey,
Rhode Island, Vermont, Virginia, Washington DC,
and Texas.
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states. In most cases, we believe
manufacturers will take this approach.
By closely aligning with California
where possible, we will allow
manufacturers to minimize research and
development (R&D) and emissions
testing, while potentially achieving
better economies of scale. It may also
reduce administrative burdens and
market logistics from having to track the
sale of multiple can designs. We
consider these to be important factor
under CAA section 183(e) which
requires us to consider economic
feasibility of controls.
States that have adopted the original
California program will likely choose to
either adopt the new California program
or eliminate their state program in favor
of the federal program. Because the
programs are similar, we expect that
most states will eventually choose the
EPA program rather than continue their
own program. We expect very little
difference in the emissions reductions
provided by the EPA and California
programs in the long term. In addition,
if EPA’s program starts in 2009, as
discussed above, this would be the same
timing states would likely target in their
program revisions.
G. Provisions for Small Gas Can
Manufacturers
As discussed in previous sections,
prior to issuing a proposal for this
proposed rulemaking, we analyzed the
potential impacts of these regulations on
small entities. As a part of this analysis,
we convened a Small Business
Advocacy Review Panel (SBAR Panel,
or ‘‘the Panel’’). During the Panel
process, we gathered information and
recommendations from Small Entity
Representatives (SERs) on how to
reduce the impact of the rule on small
entities, and those comments are
detailed in the Final Panel Report which
is located in the public record for this
rulemaking (Docket EPA–HQ–OAR–
2005–0036). Based upon these
comments, we propose to include
flexibility and hardship provisions for
gas can manufacturers. Since nearly all
gas can manufacturers (3 of 5
manufacturers as defined by SBA) are
small entities and they account for
about 60 percent of sales, the Panel
recommended to extend the flexibility
options and hardship provisions to all
gas can manufacturers. (Our proposal
today is consistent with that
recommendation.) Moreover,
implementation of the program would
be much simpler by doing so. The
flexibility provisions are incorporated
into the program requirements
described earlier in sections VIII.C
through VIII.E. The hardship provisions
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are described below. For further
discussion of the Panel process, see
section XII.C of this proposed rule and/
or the Final Panel Report.
The Panel recommended that two
types of hardship provisions be
extended to gas can manufacturers.
These entities could, on a case-by-case
basis, face hardship, and we are
proposing these provisions to provide
what could prove to be needed safety
valves for these entities. Thus, the
propose hardship provisions are as
follows:
1. First Type of Hardship Provision
Gas can manufacturers would be able
to petition EPA for limited additional
lead-time to comply with the standards.
A manufacturer would have to
demonstrate that it has taken all
possible business, technical, and
economic steps to comply but the
burden of compliance costs or would
have a significant adverse effect on the
company’s solvency. Hardship relief
could include requirements for interim
emission reductions.
2. Second Type of Hardship Provision
Gas can manufacturers would be
permitted to apply for hardship relief if
circumstances outside their control
cause the failure to comply (i.e. supply
contract broken by parts supplier), and
if failure to sell the subject containers
would have a major impact on the
company’s solvency. The terms and
timeframe of the relief would depend on
the specific circumstances of the
company and the situation involved.
For both types of hardship provisions,
the length of the hardship relief would
be established during the initial review
for not more than one year and would
be reviewed annually thereafter as
needed. As part of its application, a
company would be required to provide
a compliance plan detailing when and
how it would achieve compliance with
the standards.
IX. What Are the Estimated Impacts of
the Proposal?
A. Refinery Costs of Gasoline Benzene
Reduction
The proposed 0.62 volume percent
benzene standard would generally result
in many refiners investing in benzene
control hardware and changing the
operations in their refineries to reduce
their gasoline benzene levels. The
proposed ABT program would allow
refiners to optimize their investments,
which we believe would maximize the
benzene reductions at the lowest
possible cost. We have estimated that
the capital and operating costs that we
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believe would result from the proposed
program would average 0.13 cents per
gallon of gasoline.
In this section we summarize the
methodology used to estimate the costs
of benzene control, the scenarios we
evaluated, and our estimated costs for
the program. We also summarize the
results of our analyses of other potential
MSAT control programs. A detailed
discussion of all of these analyses is
found in Chapter 9 of the RIA.
1. Tools and Methodology
a. Linear Programming Cost Model
We considered performing our cost
assessments for this proposed program
using a linear programming (LP) cost
model. LP cost models are based on a
set of complex mathematical
representations of refineries which, for
national analyses, are usually conducted
on a regional basis. This type of refining
cost model has been used by the
government and the refining industry
for many years for estimating the cost
and other implications of changes to
fuel quality.
The design of LP models lends itself
to modeling situations where every
refinery in a region is expected to use
the same control strategy and/or has the
same process capabilities. As we began
to develop a gasoline benzene control
program with an ABT program, it
became clear that LP modeling was not
well suited for evaluating such a
program. Because refiners would be
choosing a variety of technologies for
controlling benzene, and because the
program would be national and would
include an ABT program, we initiated
development of a more appropriate cost
model, as described below. However,
the LP model remained important for
providing many of the inputs into the
new model, and for performing analyses
of other potential programs.
b. Refiner-by-Refinery Cost Model
In contrast to LP models, refinery-byrefinery cost models are useful when
individual refineries would respond to
program requirements in different ways
and/or have significantly different
process capabilities. Thus, in the case of
today’s proposed gasoline benzene
control program, we needed a model
that would accurately simulate the
variety of decisions refiners would make
at different refineries, especially in the
context of a nationwide ABT program.
For this and other related reasons, we
developed a refinery-by-refinery cost
model specifically to evaluate the
proposed benzene control program.
Our benzene cost model incorporates
the capacities of all the major units in
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each refinery in the country, as reported
by the Energy Information
Administration and in the Oil and Gas
Journal. Regarding operational
information, we know less about how
the various units are used to produce
gasoline and such factors as octane and
hydrogen costs for individual refineries.
We used the LP model to estimate these
factors on a regional basis, and we
applied the average regional result to
each refinery in that region (PADD). We
calibrated the model for each individual
refinery based on 2003 gasoline volumes
and benzene levels, which was the most
recent year for which data was
available, and found that the model
simulated the actual situation well. We
also compared cost estimates of similar
benzene control cases from both the
refinery-by-refinery model and the LP
model, and the results were in close
agreement.
Refinery-by-refinery cost models have
been used in the past by both EPA and
the oil industry for such programs as the
highway and nonroad diesel fuel sulfur
standards, and they are a proven means
for estimating the cost of compliance for
fuel control programs. For the specific
benzene cost model, we have initiated a
peer review process, and have received
some comments on the design of our
model. Although we did not receive
these comments in time to respond to
them in this proposal, we plan to
address all peer review comments in the
development of the final rule. (Based on
our initial assessment of these
comments, we do not believe that the
changes suggested would significantly
affect the projected costs of the program.
See Chapter 9 of the RIA for our initial
responses to these peer-review
comments.)
Based on our understanding of the
primary benzene control technologies
(see section VII.F above), the cost model
assumes that four technologies would be
used, as appropriate, for reducing
benzene levels. All of these technologies
focus on addressing benzene in the
reformate stream. They are (1) routing
the benzene precursors around the
reformer; (2) routing benzene precursors
to an existing isomerization unit, if
available; (3) benzene extraction
(extractive distillation); and (4) benzene
saturation. There are several restrictions
on the use of these various technologies
(such as the assumption that benzene
extraction would only be expanded in
areas with strong benzene chemical
markets) and these are incorporated into
the model.
For the proposed benzene control
program, the associated nationwide
ABT program is intended to optimize
benzene reduction by allowing each
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refinery to individually choose the most
cost-effective means of complying with
the program. To model this
phenomenon, we first establish an
estimated cost for the set of technologies
required for each refinery to meet the
standard. We then rank the refineries in
order from lowest to highest control cost
per gallon of gasoline. The model then
follows this ranking, starting with the
lowest-cost refineries, and adds
refineries and their associated control
technologies one by one until the
projected national average benzene level
reaches 0.62 volume percent. This
establishes which refineries we expect
to apply control technologies to comply,
as well as those that would generate
credits and those that would use credits
in lieu of investing in control. The sum
of the costs of the refineries expected to
invest in control provides the projected
overall cost of the program.
c. Price of Chemical Grade Benzene
The price of chemical grade benzene
is critical to the proposed program
because it defines the opportunity cost
for benzene removed using benzene
extraction and sold into the chemicals
market. According to 2004 World
Benzene Analysis produced by
Chemical Market Associates
Incorporated (CMAI), during the
consecutive five year period ending
with 2004, the price of benzene
averaged 24 dollars per barrel higher
than regular grade gasoline. During the
three consecutive year period ending
with 2004, the price of benzene
averaged 28 dollars per barrel higher
than regular grade gasoline. However,
during the first part of 2004, the price
of benzene relative to gasoline rose
steeply, primarily because of high
energy prices adding to the cost of
extracting benzene. The projected
benzene price for 2004 indicated that
the benzene price averaged 38 dollars
per barrel higher than regular grade
gasoline.
For the future, CMAI projects that the
price of benzene relative to gasoline will
return to more historic levels or lower,
in the range of $20 per barrel higher
than regular grade gasoline. We have
based our modeling on this value.
However, we have also examined the
sensitivity of the projected overall
program costs for a case where the cost
of benzene control remains at $38
higher than gasoline into the future.
d. Applying the Cost Model to Special
Cases
For the comparative cases we
modeled that involve a maximumaverage (max-avg) standard in addition
to an average benzene standard,
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modeling the costs requires a different
modeling methodology. Refineries that
the model estimates would have
benzene levels above the max-avg
standard are assumed to apply the most
cost-effective benzene reduction
technologies that the model shows
would reduce benzene levels to below
the max-avg standard. The benzene
reductions associated with meeting the
max-avg standard may or may not be
sufficient for also meeting the average
standard, depending on how stringent
the max-avg standard is relative to the
average standard. If the model indicates
that additional benzene reduction
would be necessary, these additional
benzene reductions are modeled in the
same way as the case of an average
standard only, as described above.
We also evaluated a limited number
of cases that did not include an ABT
program. In such cases, the model
assumes that all the refineries with
benzene levels below the standard
would maintain the same benzene level,
while each refinery with benzene levels
above the standard would take all the
necessary steps to reduce their benzene
levels down to the standard. If the
model shows that capital investments
are needed to achieve the necessary
benzene reduction, we assume that the
refiner installs a full sized unit to treat
the entire stream and then operates the
unit only to the extent necessary to meet
the standard.
2. Summary of Costs
a. Nationwide Costs of the Proposed
Program
We have used the refinery-by-refinery
cost model to estimate the costs of the
proposed program, with an average
gasoline benzene content standard of
0.62 volume percent and the proposed
ABT program. In general, the cost model
indicates that among the four primary
reformate-based technologies, benzene
extraction would be the most cost
effective. The next most cost effective
technologies are benzene precursor
rerouting, and rerouting coupled with
isomerization. The model indicates that
benzene saturation would be the least
cost-effective, but only marginally so in
the larger refineries.
Our refinery-by-refinery model
estimates that 92 refineries of the total
115 gasoline-producing refineries in the
U.S. would have to put in new capital
equipment or change their refining
operations to reduce the benzene levels
in their gasoline. Of these refineries 25
would use benzene precursor removal,
32 refineries would use benzene
precursor removal coupled with
isomerization, 24 would use extraction,
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and 11 would use benzene saturation.
The analysis projects that 43 refineries
would reduce their benzene levels to the
proposed benzene standard or lower,
while 49 refineries would reduce their
benzene levels but still would need to
purchase credits to comply with the
average benzene standard. Including the
refineries with benzene levels currently
below 0.62, we project that there would
be a total of 62 refineries producing
gasoline with benzene levels at 0.62 or
lower. The model assumes that those
with benzene levels lower than 0.62
volume percent would generate credits
for sale to other refineries. Finally, the
model projects that there would be 6
refineries that would take no benzene
reduction action and comply with the
proposed program solely through the
use of benzene credits.
The refinery model estimates that the
proposed benzene standard would cost
0.13 cents per gallon, averaged over the
entire U.S. gasoline pool. (When
averaged only over those refineries
which are assumed to take steps to
reduce their benzene levels, the average
cost would be 0.19 cents per gallon.)
This per-gallon cost would result from
an industry-wide investment in capital
equipment of $500 million to reduce
gasoline benzene levels. This would
amount to an average of $5 million in
capital investment in each refinery that
adds such equipment.284
We also estimated annual aggregate
costs associated with the proposed new
fuel standard. As shown in Table IX.A–
1, these costs are projected to begin at
$186 million in 2011 and increase over
time as fuel demand increases.
TABLE IX.A–1.—ANNUAL AGGREGATE FUEL COSTS
2011
2013
2015
2017
2019
2020
$185,533,000 .......................................................................
$191,873,000
$198,283,000
$204,212,000
$209,875,000
$212,606,000
Several observations can be made
from these results from our nationwide
analysis. First, significantly reducing
gasoline benzene levels to low levels,
coupled with the flexibility of an ABT
program, will incur fairly modest costs.
This is primarily because we expect that
refiners would optimize their benzene
control strategies, resulting in large
benzene reductions at a low overall
program cost. With high benzene prices
relative to those of gasoline projected to
continue (even if they drop from the
recent very high levels), extraction
would be a very low cost technology—
the primary reason why the cost of the
overall program is very low. Also,
precursor rerouting, either with or
without isomerization in an existing
unit, is a low-cost technology requiring
little or no capital to realize. The model
concludes that even the higher-cost
benzene saturation technology would be
fairly cost-effective overall because
larger refineries that install this
technology would take advantage of
their economies of scale.
b. Regional Distribution of Costs
The benzene reductions estimated by
the cost model and associated costs vary
significantly by region. Table IX.A–2
summarizes the initial benzene levels
and the projected benzene levels after
refiners take anticipated steps to reduce
the benzene in their gasoline and the
estimated per-gallon costs for complying
with the proposed benzene standard.
Table IX.A–2 shows that under the
proposed program the largest benzene
reductions occur in the areas with the
highest benzene levels. This is expected
as many of these refineries are not doing
anything to reduce their gasoline
benzene levels today and simple, lowcost technologies can be employed to
realize large reductions in their benzene
levels. In PADDs 1 and 3, which have
significant benzene control today to
meet the RFG requirements, a more
modest benzene reduction would occur.
Many of the refineries producing fuel
for sale in PADDs 1 and 3 cannot reduce
their benzene levels further because
they are already extracting all the
benzene that they can. Extraction is the
technology most used in PADDs 1 and
3, resulting in a much lower average
cost for reducing benzene in these
regions.
For comparison, we also modeled a
program where the 0.62 vol% average
standard was supplemented by a
maximum average benzene cap
standard, as described in section VII
above. We did not propose such a
maximum average standard because the
main effect would simply be to shift
emission reductions from one region of
the country to another with no change
in overall emission reductions. Table
IX.A–2 shows that a maximum average
standard would increase costs slightly
nationwide, but that PADD 2 benzene
levels, already above the standard,
would rise while other areas improved.
TABLE IX.A–2.—CURRENT AND PROJECTED BENZENE LEVELS AND COSTS BY PADD
[$2002, 7% ROI before taxes]
PADD
1
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Current Benzene Level (vol%) .................................................................
Projected Benzene Level (vol%) .............................................................
Cost (c/gal) ...............................................................................................
Projected Benzene Level (vol%) (With 1.3 vol% Max-Avg Std) .............
Cost (c/gal) ...............................................................................................
2
0.66
0.51
0.05
0.50
0.06
3
1.32
0.73
0.25
0.75
0.22
c. Cost Effects of Different Standards
We also estimated the benzene
reduction costs for other benzene
additional hydrogen, but rather includes these in
0.86
0.55
0.05
0.56
0.03
1.54
0.95
0.40
0.90
0.43
U.S.
1.87
1.04
0.72
0.88
1.18
reduction levels, as summarized in
Table IX.A–3. The cost model estimates
that a 0.52 volume percent benzene
284 The modeling does not separate out capital
costs for the recovery of lost octane and supplying
5
(w/o CA)
4
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the operating cost estimates. Therefore, actual
capital costs maybe somewhat greater.
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0.62
0.125
0.62
0.130
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standard with an ABT program 285 is the
maximum benzene reduction possible
when each refinery employs the
maximum appropriate reformate
benzene control (that is, benzene
extraction whenever possible, and
benzene saturation otherwise).
TABLE IX.A–3.—COSTS OF VARIOUS
POTENTIAL
BENZENE
CONTROL
STANDARDS
[$2002, 7% ROI before taxes]
Average standard
(vol%)
0.62
0.65
0.60
0.52
Cost
(cents/gallon)
(Proposed Standard) ....
.......................................
.......................................
.......................................
0.13
0.09
0.15
0.36
The results in Table IX.A–3 indicate
that the cost for reducing benzene levels
is not very sensitive to the benzene
standard in the range from 0.60 to 0.65
volume percent benzene. This is
because we project that standards in this
range would not require many of the
smaller or otherwise higher-cost
refineries to employ benzene saturation,
which is the highest cost technology.
Also, in this range of potential
standards, the ABT program would
allow the refining industry to optimize
the benzene control technologies they
apply. The need for all refineries to use
either benzene saturation or benzene
extraction to comply with a 0.52 vol%
standard explains the much higher cost
for a program with a standard that
range.
We also examined the effect of the
ABT program on cost. Without ABT, we
assume that the standard would be met
by all refineries. To achieve a national
average level of 0.62 vol% benzene
without an ABT program would require
an absolute standard of 0.73 vol%. We
estimate that such a program would
result in a nationwide average cost of
0.25 cents per gallon, about double the
cost of the program with ABT.
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d. Effect on Cost Estimates of Higher
Benzene Prices
As described above, we also
performed a sensitivity analysis to
estimate the costs of the proposed
program if the recent very high prices
for chemical grade benzene continue
285 The cost model projects that this standard
would require an ABT program because many of the
refineries modeled would not be able to achieve
this standard. These refineries would have to rely
on the purchase of credits from other refineries
which are already below this benzene level, or other
refineries which could install benzene control
technology to get their benzene levels below this
standard. This scenario assumes a fully utilized
credit program.
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into the future. We estimate that at an
average benzene price of $38 dollars
above that for gasoline, the program
would cost 0.08 cents per gallon less on
average nationwide.
3. Economic Impacts of MSAT Control
Through Gasoline Sulfur and RVP
Control and a Total Toxics Standard
As discussed above in section VII, we
have considered two approaches to fuelrelated MSAT control that would
involve increasing the stringency of two
existing emission control programs, the
gasoline sulfur program and the gasoline
volatility program. We estimated the
cost of programs that would further
reduce the sulfur content and Reid
vapor pressure (RVP) of gasoline. For
these costs estimates, the LP refinery
model was used to estimate the costs for
the year 2010, including the fuel
economy impacts. We summarize these
costs here and provide detailed analyses
in Chapter 9 of the RIA.
For sulfur control, we estimated the
costs of reducing U.S. gasoline sulfur
levels down to 10 ppm from the 30 ppm
sulfur level required for Tier 2 sulfur
control. The costs are based on
revamping current hydrotreaters
installed to meet the 30 ppm sulfur
standard. We estimate that reducing
gasoline sulfur down to 10 ppm would
cost 0.51 cents per gallon, taking into
account the fuel economy effects. The
analysis also estimates that U.S. refiners
would invest $1.3 billion in new capital
to achieve this sulfur reduction.
We also estimated costs for lowering
summertime gasoline RVP down to a
maximum of 7.8 or 7.0 RVP from the
current average for non-RVP controlled
gasoline of 9.0 RVP. The estimated
volume of gasoline required to meet an
additional low RVP requirement was
assumed to be equivalent to half of the
volume of the reformulated gasoline
sold within the PADD, applied to the
conventional gasoline sold within the
PADD. This simple means of estimating
the volume of gasoline affected by
future additional RVP control programs
was used because the analysis of
possible new low RVP programs
established for complying with the 8
hour ozone National Ambient Air
Quality Standards (NAAQS) was not
completed when the cost analysis was
initiated. The per-gallon cost is not
expected to vary much by the size of the
program. The cost analysis estimates
that reducing RVP down to 7.8 RVP
would cost 0.23 cents per gallon. The
analysis also estimates that U.S. refiners
would invest $121 million in new
capital to achieve this level of RVP
control. The cost analysis estimates that
reducing RVP down to 7.0 RVP would
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cost 0.40 cents per gallon. Meeting a 7.0
RVP standard is projected to cause U.S.
refiners to invest $184 million in new
capital to achieve this level of RVP
control.
We have also evaluated the costs of
programs that would control total air
toxics. These programs, the analyses of
which are also found in Chapter 9 of the
RIA, would all be more costly than the
proposed program.
B. What Are the Vehicle Cost Impacts?
In assessing the economic impact of
setting cold temperature emission
standards, we have made a best estimate
of the necessary vehicle modifications
and their associated costs. In making
our estimates we have relied on our own
technology assessment, which includes
information supplied by individual
manufacturers and our own in-house
testing. Estimated costs typically
include variable costs (for hardware and
assembly time) and fixed costs (for
research and development, retooling,
and certification). All costs are
presented in 2003 dollars. Full details of
our cost analysis can be found in
Chapter 8 of the draft RIA.
As described in section VI, we are not
expecting hardware changes to Tier 2
vehicles in response to new cold
temperature standards. Tier 2 vehicles
are already being equipped with very
sophisticated emissions control systems.
We expect manufacturers to use these
systems to minimize emissions at cold
temperatures. We were able to
demonstrate significant emissions
reductions from a Tier 2 vehicle through
recalibration alone. In addition, a
standard based on averaging allows
some vehicles to be above the numeric
standard as long as those excess
emissions are offset by vehicles below
the standard. Averaging would help
manufacturers in cases where they are
not able to achieve the numeric
standard for a particular vehicle group,
thus helping manufacturers avoid costly
hardware changes. The phase-in of
standards and emissions credits
provisions also help manufacturers
avoid situations where expensive
vehicle modifications would be needed
to meet a new cold temperature NMHC
standard. Therefore, we are not
projecting hardware costs or additional
assembly costs associated with meeting
new cold temperature NMHC emissions
standards.
Manufacturers would incur research
and development (R&D) costs associated
with a new cold temperature standard,
and some likely would need to upgrade
testing facilities to handle an increased
number of cold tests during vehicle
development. We have estimated the
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fixed costs associated with R&D and test
facilities. We project that manufacturers
would recover R&D costs over a fiveyear period and their facilities costs
over a ten-year period. Long-term
impacts on engine costs are expected to
decrease as manufacturers fully
amortize their fixed costs. Because
manufacturers recoup fixed costs over a
large volume of vehicles, average per
vehicle costs due to the new cold
temperature NMHC standards are
expected to be low. We project that the
average incremental costs associated
with the new cold temperature
standards would be less than $1 per
vehicle.
We are not anticipating additional
costs for the proposed new evaporative
emissions standard. As discussed in
section VI, we expect that
manufacturers will continue to produce
50-state evaporative systems that meet
LEV II standards. Therefore,
harmonizing with California’s LEV–II
evaporative emission standards would
streamline certification and be an ‘‘antibacksliding’’ measure. It also would
codify the approach manufacturers have
already indicated they are taking for 50state evaporative systems.
We also estimated annual aggregate
costs associated with the new cold
temperature emissions standards. These
costs are projected to increase with the
phase-in of standards and peak in 2014
at about $13.4 million per year, then
decrease as the fixed costs are fully
amortized. The projected aggregate costs
are summarized below, with annual
estimates provided in Chapter 8 of the
RIA.
TABLE IX.B–1.—ANNUAL AGGREGATE COSTS
2010
2012
$11,119,000 ..........
2014
$12,535,000
C. What Are the Gas Can Cost Impacts?
For gas cans, we have made a best
estimate of the necessary technologies
and their associated costs. Estimated
costs include variable costs (for
hardware and assembly time) and fixed
costs (for research and development,
retooling, and certification). The
analysis also considers fuels savings
associated with low emissions gas cans.
Cost estimates based on the projected
technologies represent an expected
change in the cost of gas cans as they
begin to comply with new emission
standards. All costs are presented in
2003 dollars. Full details of our cost
analysis, including fuel savings, can be
found in Chapter 10 of the Draft RIA.
Table IX.C–1 summarizes the
projected near-term and long-term per
unit average costs to meet the new
emission standards. Long-term impacts
on gas cans are expected to decrease as
2016
$13,406,000
2018
$12,207,000
2020
$10,682,000
$0
manufacturers fully amortize their fixed
costs. We project that manufacturers
will generally recover their fixed costs
over a five-year period, so these costs
disappear from the analysis after the
fifth year of production. These estimates
are based on the manufacturing cost
rather than predicted price increases.286
The table also shows our projections of
average fuel savings over the life of the
gas can. Fuel savings can be estimated
based on the VOC emissions reductions
due to gas can controls.
With current and projected estimates
of gas can sales, we translate these costs
into projected direct costs to the nation
for the new emission standards in any
year. A summary of the annual aggregate
costs to manufacturers is presented in
Table IX.C–2. The annual cost savings
due to fuel savings start slowly, then
increase as greater numbers of
compliant gas cans enter the market.
Table IX.C–2 also presents a summary of
the estimated annual fuel savings.
Aggregate costs are projected to peak in
TABLE IX.C–1.—ESTIMATED AVERAGE 2013 at about $51 million and then drop
to about $29 million once fixed costs are
GAS CAN COSTS AND LIFETIME
recovered. The change in numbers
FUEL SAVINGS
beyond 2015 occurs due to projected
growth in gas can sales and population.
Cost
Near-Term Costs ..............................
Long-Term Costs ..............................
Fuel Savings (NPV) ..........................
$2.69
1.52
4.24
TABLE IX.C–2.—TOTAL ANNUALIZED COSTS AND FUEL SAVINGS
2009
Costs ................................................................................................................
Fuel Saving ......................................................................................................
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D. Cost Per Ton of Emissions Reduced
We have calculated the cost per ton of
HC, benzene, total MSATs, and PM
emissions reductions associated with
the proposed fuel, vehicle, and gas can
programs using the costs described
above and the emissions reductions
described in section V. More detail on
the costs, emissions reductions, and cost
286 These cost numbers may not necessarily
reflect actual price increases as manufacturer
production costs, perceived product enhancements,
and other market impacts will affect actual prices
to consumers.
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$49,112,000
14,381,000
2013
2015
$51,228,000
76,037,000
$28,772,000
92,686,000
2020
$31,767,000
98,861,000
per ton estimates can be found in the
draft RIA. We have calculated the costs
per ton using the net present value of
the annualized costs of the program,
including gas can fuel savings, from
2009 through 2030 and the net present
value of the annual emission reductions
through 2030. We have also calculated
the cost per ton of emissions reduced in
the year 2030 using the annual costs and
emissions reductions in that year alone.
This number represents the long-term
cost per ton of emissions reduced. For
fuels, the cost per ton estimates include
costs and emission reductions that will
occur from all motor vehicles and
nonroad engines fueled with
gasoline.287
287 The proposed standards do not apply to
nonroad engines, since section 202 (l) authorizes
controls only for ‘‘motor vehicles,’’ which does not
include nonroad vehicles. CAA section 216 (2).
However, we are reducing benzene in all gasoline,
including that used in nonroad equipment.
Therefore, we are including both the costs and the
benzene emissions reductions associated with the
fuel used in nonroad equipment.
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For vehicles and gas cans, we are
proposing to establish NMHC and HC
standards, respectively, which would
also reduce benzene and other VOCbased toxics. For vehicles, we are also
expecting direct PM reductions due to
the proposed NMHC standard.288
Section V provides an overview of how
we are estimating benzene and PM
reductions resulting from the NMHC
standards for vehicles and benzene
reductions resulting from the HC
standard for gas cans. We have not
attempted to apportion costs across
these various pollutants for purposes of
the cost per ton calculations since there
is no distinction in the technologies, or
associated costs, used to control the
pollutants. Instead, we have calculated
costs per ton by assigning all costs to
each individual pollutant. If we
apportioned costs among the pollutants,
the costs per ton presented here would
be proportionally lowered depending on
what portion of costs were assigned to
the various pollutants.
The results for HC for vehicles and
gas cans are provided in Table IX.D–1
using both a three percent and a seven
percent social discount rate. Again, this
analysis assumes that all costs are
assigned to HC control. The discounted
cost per ton of HC reduced for the
proposal as a whole would be $0
because the fuel savings from gas cans
offsets the costs of gas can and vehicle
controls. The table presents these as $0
per ton, rather than calculating a
negative value that has no clear
meaning. For vehicles in 2030, the cost
per ton is $0 because by 2030 all fixed
costs have been recovered and there are
no variable costs estimated for the
proposed vehicle program.289
The cost per ton estimates for each
individual program are presented
separately in the tables below, and are
part of the justification for each of the
programs. For informational purposes,
we also present the cost per ton for the
three programs combined.
TABLE IX.D–1.—HC AGGREGATE COST PER TON AND LONG-TERM ANNUAL COST PER TON
[$2003]
Discounted
lifetime cost
per ton at 3%
Discounted
lifetime cost
per ton at 7%
Long-term cost
per ton in
2030
$14
230
0
0
$18
250
0
0
$0
180
0
0
Vehicles .......................................................................................................................................
Gas Cans (without fuel savings) .................................................................................................
Gas Cans (with fuel savings) ......................................................................................................
Combined (with fuel savings) ......................................................................................................
The cost per ton of benzene
reductions for fuels, vehicles, and gas
cans are shown in Table IX.D–2 using
the same methodology as noted above
for HC. The results are calculated by
assigning all costs to benzene control.
TABLE IX.D–2.—BENZENE AGGREGATE COST PER TON AND LONG-TERM ANNUAL COST PER TON
[$2003]
Discounted
lifetime cost
per ton at 3%
Fuels ............................................................................................................................................
Vehicles .......................................................................................................................................
Gas Cans (without fuels savings) ................................................................................................
Gas Cans (with fuel savings) ......................................................................................................
Combined (with fuel savings) ......................................................................................................
The cost per ton of overall MSAT
reductions for fuels, vehicles, and gas
cans are shown in Table IX.D–3 using
the same methodology as noted above
for HC and benzene. The results are
Discounted
lifetime cost
per ton at 7%
Long-term cost
per ton in
2030
$10,900
260
27,800
0
3,400
11,100
340
30,900
0
3,600
11,400
0
21,600
0
2,400
calculated by assigning all costs to
MSAT control.
TABLE IX.D–3.—MSAT AGGREGATE COST PER TON AND LONG-TERM ANNUAL COST PER TON
[$2003]
Discounted
lifetime cost
per ton at 3%
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Fuels ............................................................................................................................................
Vehicles .......................................................................................................................................
Gas Cans (without fuel savings) .................................................................................................
Gas Cans (with fuel savings) ......................................................................................................
Combined (with fuel savings) ......................................................................................................
288 Again, although gasoline PM is not a mobile
source air toxic, the rule will result in emission
reductions of gasoline PM which reductions are
accounted for in our analysis.
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289 We note that in determining whether the
proposed vehicle controls represent the greatest
emissions reductions achievable considering costs,
we have considered the proposed cold-start
standards separately from any other proposed
control program. Similarly, in considering whether
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Discounted
lifetime cost
per ton at 7%
Long-term cost
per ton in
2030
$10,900
40
1,800
0
710
$11,100
53
2,000
0
780
$11,400
0
1,400
0
450
the proposed controls for gas cans represent the best
available control considering economic feasibility,
we considered the proposed gas can standards
separately from any other proposed control
program.
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We have also calculated a cost per ton
for direct PM reductions for vehicles.
Again, this analysis assigns all related
costs to direct PM reductions.
TABLE IX.D–4.—DIRECT PM AGGREGATE COST PER TON AND LONG-TERM ANNUAL COST PER TON
($2003)
Discounted
lifetime cost
per ton at 3%
Discounted
lifetime cost
per ton at 7%
Long-term cost
per ton in
2030
$620
$820
$0
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Vehicles .......................................................................................................................................
detail why these benefits are not
quantified.
E. Benefits
This section presents our analysis of
the health and environmental benefits
that can be expected to occur as a result
of the proposed standards throughout
the period from initial implementation
through 2030. In terms of emission
benefits, we expect to see significant
reductions in mobile source air toxics
(MSATs) from the proposed vehicle,
fuel and gas can standards, reductions
in VOCs (an ozone precursor) from the
proposed cold temperature vehicle and
gas can standards, and reductions in
direct PM2.5 from the proposed cold
temperature vehicle standards. When
translating emission benefits to health
effects and monetized values, however,
we only quantify the PM-related
benefits associated with the proposed
cold temperature vehicle standards.
The reductions in PM from the
proposed cold temperature vehicle
standards would result in significant
reductions in premature deaths and
other serious human health effects, as
well as other important public health
and welfare effects. We estimate that in
2030, the benefits we are able to
monetize are expected to be
approximately $6.5 billion using a 3
percent discount rate and $5.9 billion
using a 7 percent discount rate. Total
social costs of the entire proposal for the
same year (2030) are $205 million.
Details on the costs of each of the
proposed controls are in section IX.F.
These estimates, and all monetized
benefits presented in this section, are in
year 2003 dollars.
We demonstrate that the proposed
standards would reduce cancer and
noncancer risk from reduced exposure
to MSATs (as described in Section IV of
this preamble). However, we do not
translate this risk reduction into
benefits. We also do not quantify the
benefits related to ambient reductions in
ozone due to the VOC emission
reductions expected to occur as a result
of the proposed standards. The
following section describes in more
1. Unquantified Health and
Environmental Benefits
This benefit analysis estimates
improvements in health and human
welfare that can be expected as a result
of the proposed standards, and
monetizes those benefits. The benefits
would come from reductions in
emissions of air toxics (including
benzene, 1,3-butadiene, formaldehyde,
acetaldehyde, acrolein, naphthalene,
and other air toxic pollutants discussed
in Section III), ambient ozone (as a
result of VOC controls), and direct PM2.5
emissions.
While there will be benefits
associated with air toxic pollutant
reductions, notably with regard to
reductions in exposure and risk (see
Section IV, above), we do not attempt to
monetize those benefits. This is
primarily because available tools and
methods to assess air toxics risk from
mobile sources at the national scale are
not adequate for extrapolation to
incidence estimations or benefits
assessment. The best suite of tools and
methods currently available for
assessment at the national scale are
those used in the National Scale Air
Toxics Assessment (NATA; these tools
are discussed in Section IV.A). The EPA
Science Advisory Board specifically
commented in their review of the 1996
National Air Toxics Assessment (NATA)
that these tools were not yet ready for
use in a national-scale benefits analysis,
because they did not consider the full
distribution of exposure and risk, or
address sub-chronic health effects.290
While EPA has since improved the
tools, there remain critical limitations
for estimating incidence and assessing
benefits of reducing mobile source air
toxics. We continue to work to address
these limitations, and we are exploring
the feasibility of a quantitative benefits
assessment for air toxics as part of a case
study being done for benzene as part of
290 Science Advisory Board. 2001. NATA–
Evaluating the National-Scale Air Toxics
Assessment for 1996—an SAB Advisory. https://
www.epa.gov/ttn/atw/sab/sabrev.html.
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the ongoing update to the Section 812
retrospective and prospective studies.291
We also do not estimate the
monetized benefits of VOC controls in
this benefits analysis. Though VOCs
would be demonstrably reduced as a
result of the cold temperature vehicle
standards, we assume that these
emissions would not have a measurable
impact on ozone formation since the
standards seek to reduce VOC emissions
at cold ambient temperatures and ozone
formation is primarily a warm ambient
temperature issue. The gas can controls
would likely result in ozone benefits,
though we do not attempt to monetize
those benefits. This is primarily due to
the magnitude of, and uncertainty
associated with, the estimated changes
in ambient ozone associated with the
proposed standards. In Section IV.C., we
discuss that the ozone modeling
conducted for the proposed gas can
standards results in a net reduction in
the population weighted ozone design
value metric measured within the
modeled domain (37 Eastern states and
the District of Columbia). The net
improvement is very small, however,
and would likely lead to negligible
monetized benefits. Instead, we
acknowledge that this analysis may
underestimate the benefits associated
with reductions in ozone precursor
emissions achieved by the various
proposed standards. We discuss these
benefits qualitatively within the
Regulatory Impact Analysis.
Table IX.E–1 lists each of the MSAT
and ozone health and welfare effects
that remain unquantified because of
current limitations in the methods or
available data. This table also includes
the PM-related health and welfare
effects that also remain unquantified
due to current method and data
limitations. Chapter 12 of the Regulatory
Impact Analysis for the proposed
standards provides a qualitative
description of the health and welfare
effects not quantified in this analysis.
291 The analytic blueprint for the Section 812
benzene case study can be found at https://
www.epa.gov/air/sect812/appendixi51203.pdf.
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TABLE IX.E–1.—UNQUANTIFIED AND NON-MONETIZED EFFECTS
Pollutant/effects
Effects not included in primary estimates—changes in:
Ozone Health a ..........................................................................
Ozone Welfare ..........................................................................
PM Health c ................................................................................
PM Welfare ................................................................................
MSAT Health .............................................................................
MSAT Welfare ...........................................................................
Premature mortality: short term exposures b.
Hospital admissions: respiratory.
Emergency room visits for asthma.
Minor restricted-activity days.
School loss days.
Asthma attacks.
Cardiovascular emergency room visits.
Acute respiratory symptoms.
Chronic respiratory damage.
Premature aging of the lungs.
Non-asthma respiratory emergency room visits.
Exposure to UVb (+/¥) e.
Decreased outdoor worker productivity.
Agricultural yields for
—commercial forests.
—some fruits and vegetables.
—non-commercial crops.
Damage to urban ornamental plants.
Impacts on recreational demand from damaged forest aesthetics.
Ecosystem functions.
Exposure to UVb (+/¥) e.
Premature mortality—short term exposures d.
Low birth weight.
Pulmonary function.
Chronic respiratory diseases other than chronic bronchitis.
Non-asthma respiratory emergency room visits.
Exposure to UVb (+/¥) e.
Visibility in many Class I areas.
Residential and recreational visibility in non-Class I areas.
Soiling and materials damage.
Damage to ecosystem functions.
Exposure to UVb (+/¥) e.
Cancer (benzene, 1,3-butadiene, formaldehyde, acetaldehyde, naphthalene).
Anemia (benzene).
Disruption of production of blood components (benzene).
Reduction in the number of blood platelets (benzene).
Excessive bone marrow formation (benzene).
Depression of lymphocyte counts (benzene).
Reproductive and developmental effects (1,3-butadiene).
Irritation of eyes and mucus membranes (formaldehyde).
Respiratory irritation (formaldehyde).
Asthma attacks in asthmatics (formaldehyde).
Asthma-like symptoms in non-asthmatics (formaldehyde).
Irritation of the eyes, skin, and respiratory tract (acetaldehyde).
Upper respiratory tract irritation and congestion (acrolein).
Direct toxic effects to animals.
Bioaccumulation in the food chain.
Damage to ecosystem function.
Odor.
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a In addition to primary economic endpoints, there are a number of biological responses that have been associated with ozone health effects
including increased airway responsiveness to stimuli, inflammation in the lung, acute inflammation and respiratory cell damage, and increased
susceptibility to respiratory infection.
b EPA sponsored a series of meta-analyses of the ozone mortality epidemiology literature, published in the July 2005 volume of the journal Epidemiology, which found that short-term exposures to ozone may have a significant effect on daily mortality rates, independent of exposure to
PM. EPA is currently considering how to include an estimate of ozone mortality in its primary benefits analyses.
c In addition to primary economic endpoints, there are a number of biological responses that have been associated with PM health effects including morphological changes and altered host defense mechanisms. The public health impact of these biological responses may be partly represented by our quantified endpoints.
d While some of the effects of short term exposures are likely to be captured in the estimates, there may be premature mortality due to short
term exposure to PM not captured in the cohort study upon which the primary analysis is based.
e May result in benefits or disbenefits.
2. Quantified Human Health and
Environmental Effects of the Proposed
Cold Temperature Vehicle Standard
In this section we discuss the PM2.5
benefits of the proposed cold
temperature vehicle standard. To
estimate PM2.5 benefits, we rely on a
benefits transfer technique. The benefits
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transfer approach uses as its foundation
the relationship between emission
reductions and ambient PM2.5
concentrations modeled across the
contiguous 48 states (and DC) for the
Clean Air Nonroad Diesel (CAND)
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proposal.292 For a given future year, we
first calculate the ratio between CAND
direct PM2.5 emission reductions and
direct PM2.5 emission reductions
associated with the proposed cold
temperature vehicle control standard
292 See
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(proposed emission reductions/CAND
emission reductions). We multiply this
ratio by the percent that direct PM2.5
contributes towards populationweighted reductions in total PM2.5 due
to the CAND standards. This calculation
results in a ‘‘benefits apportionment
factor’’ for the relationship between
direct PM emissions and primary PM2.5,
which is then applied to the BenMAPbased incidence and monetized benefits
from the CAND proposal. In this way,
we apportion the results of the proposed
CAND analysis to its underlying direct
PM emission reductions and scale the
apportioned benefits to reflect
differences in emission reductions
between the modeled CAND control
option and the proposed standards.293
This benefits transfer method is
consistent with the approach used in
other recent mobile and stationary
source rules.294
Table IX.E–2 presents the primary
estimates of reduced incidence of PMrelated health effects for the years 2020
and 2030 for the proposed cold
temperature vehicle control
strategies.295 In 2030, we estimate that
PM-related annual benefits would result
15909
in approximately 910 fewer premature
fatalities, 590 fewer cases of chronic
bronchitis, 1,600 fewer non-fatal heart
attacks, and 940 fewer hospitalizations
(for respiratory and cardiovascular
disease combined). In addition, we
estimate that the emission controls
would reduce days of restricted activity
due to respiratory illness by about
620,000 days and reduce work-loss days
by about 110,000 days. We also estimate
substantial health improvements for
children from reduced upper and lower
respiratory illness, acute bronchitis, and
asthma attacks.
TABLE IX.E–2.—ESTIMATED ANNUAL REDUCTIONS IN INCIDENCE OF HEALTH EFFECTS RELATED TO THE PROPOSED
COLD TEMPERATURE VEHICLE STANDARD a
2020 Annual
incidence
reduction
Health effect
PM-Related Endpoints:
Premature Mortality b
Adult, age 30+ and Infant, age <1 year ...........................................................................................................
Chronic bronchitis (adult, age 26 and over) .....................................................................................................
Non-fatal myocardial infarction (adult, age 18 and over) .................................................................................
Hospital admissions—respiratory (all ages) c ...................................................................................................
Hospital admissions—cardiovascular (adults, age >18) d ................................................................................
Emergency room visits for asthma (age 18 years and younger) ....................................................................
Acute bronchitis, (children, age 8–12) .............................................................................................................
Lower respiratory symptoms (children, age 7–14) ...........................................................................................
Upper respiratory symptoms (asthmatic children, age 9–18) ..........................................................................
Asthma exacerbation (asthmatic children, age 6–18) ......................................................................................
Work Loss Days ...............................................................................................................................................
Minor restricted activity days (adults age 18–65) ............................................................................................
480
330
820
260
220
360
790
9,400
7,100
12,000
63,000
370,000
2030 Annual
incidence
reduction
910
590
1,600
540
400
630
1,400
17,000
13,000
21,000
110,000
620,000
a Incidence
is rounded to two significant digits. Estimates represent benefits from the proposed rule nationwide, excluding Alaska and Hawaii.
adult mortality based upon studies by Pope, et al 2002.296 PM-related infant mortality based upon studies by Woodruff, Grillo, and
Schoendorf,1997.297
c Respiratory hospital admissions for PM include admissions for chronic obstructive pulmonary disease (COPD), pneumonia and asthma.
d Cardiovascular hospital admissions for PM include total cardiovascular and subcategories for ischemic heart disease, dysrhythmias, and heart
failure.
b PM-related
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PM also has numerous documented
effects on environmental quality that
affect human welfare. These welfare
effects include direct damages to
property, either through impacts on
material structures or by soiling of
surfaces, and indirect economic
damages through the loss in value of
recreational visibility or the existence
value of important resources. Additional
information about these welfare effects
can be found in Chapter 12 of the
Regulatory Impact Analysis prepared for
this proposal.
3. Monetized Benefits
Table IX.E–3 presents the estimated
monetary value of reductions in the
incidence of those health effects we are
able to monetize for the proposed cold
temperature vehicle standard. Total
annual PM-related health benefits are
estimated to be approximately $6.5 or
$5.9 billion in 2030 (3 percent and 7
percent discount rate, respectively).
These estimates account for growth in
real gross domestic product (GDP) per
capita between the present and 2030.
Table IX.E–3 indicates with a ‘‘B’’
those additional health and
environmental benefits of the rule that
we are unable to quantify or monetize.
These effects are additive to the estimate
of total benefits, and are related to the
following sources:
• There are many human health and
welfare effects associated with PM,
ozone, and toxic air pollutant
reductions that remain unquantified
because of current limitations in the
methods or available data. A listing of
the benefit categories that could not be
quantified or monetized in our benefit
estimates are provided in Table IX.E–1.
293 Note that while the proposed regulations also
control VOCs, which contribute to PM formation,
the benefits transfer scaling approach only scales
benefits based on NOX, SO2, and direct PM
emission reductions. PM benefits will likely be
underestimated as a result, though we are unable
to estimate the magnitude of the underestimation.
294 See: Clean Air Nonroad Diesel final rule (69
FR 38958, June 29, 2004); Nonroad Large SparkIgnition Engines and Recreational Engines
standards (67 FR 68241, November 8, 2002); Final
Industrial Boilers and Process Heaters NESHAP (69
FR 55217, September 13, 2004); Final Reciprocating
Internal Combustion Engines NESHAP (69 FR
33473, June 15, 2004); Final Clean Air Visibility
Rule (EPA–452/R–05–004, June 15, 2005); Ozone
Implementation Rule (documentation forthcoming).
295 The ‘‘primary estimate’’ refers to the estimate
of benefits that reflects the suite of endpoints and
assumptions that EPA believes yields the expected
value of air quality improvements related to the
proposed standards. The impact that alternative
endpoints and assumptions have on the benefit
estimates are explored in appendixes to the RIA.
296 Pope, C.A., III, R.T. Burnett, M.J. Thun, E.E.
Calle, D. Krewski, K. Ito, and G.D. Thurston. 2002.
‘‘Lung Cancer, Cardiopulmonary Mortality, and
Long-term Exposure to Fine Particulate Air
Pollution.’’ Journal of American Medical
Association 287:1132–1141.
297 Woodruff, T.J., J. Grillo, and K.C. Schoendorf.
1997. ‘‘The Relationship Between Selected Causes
of Postneonatal Infant Mortality and Particulate
Infant Mortality and Particulate Air Pollution in the
United States.’’ Environmental Health Perspectives
105(6):608–612.
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• The PM benefits scaled transfer
approach, derived from the Clean Air
Nonroad Diesel rule, does not account
for VOCs as precursors to ambient PM2.5
formation. To the extent that VOC
emission reductions associated with the
proposed regulations contribute to
reductions in ambient PM2.5, this
analysis does not capture the related
health and environmental benefits of
those changes.
• The PM air quality model only
captures the benefits of air quality
improvements in the 48 states and DC;
PM benefits for Alaska and Hawaii are
not reflected in the estimate of benefits.
TABLE IX.E–3.—ESTIMATED ANNUAL MONETARY VALUE OF REDUCTIONS IN INCIDENCE OF HEALTH AND WELFARE
EFFECTS RELATED TO THE PROPOSED COLD TEMPERATURE VEHICLE STANDARD
[Millions of 2003$] a b
Health effect
2020
Estimated
value of
reductions
Pollutant
PM-Related Premature mortality c, d:
Adult, 30+ years and Infant, <1 year.
3 percent discount rate ...................................................................
7 percent discount rate ...................................................................
Chronic bronchitis (adults, 26 and over) .......................................................
Non-fatal acute myocardial infarctions:
3 percent discount rate ...................................................................
7 percent discount rate ...................................................................
Hospital admissions for respiratory causes ..................................................
Hospital admissions for cardiovascular causes ............................................
Emergency room visits for asthma ...............................................................
Acute bronchitis (children, age 8–12) ...........................................................
Lower respiratory symptoms (children, age 7–14) .......................................
Upper respiratory symptoms (asthma, age 9–11) ........................................
Asthma exacerbations ...................................................................................
Work loss days ..............................................................................................
Minor restricted activity days (MRADs) .........................................................
Monetized Total e:
Base estimate.
3 percent discount rate ...................................................................
7 percent discount rate ...................................................................
2030
Estimated
value of
reductions
PM2.5 .................................................
...........................................................
PM2.5 .................................................
$3,100
2,800
150
$6,000
5,400
270
...........................................................
PM2.5 .................................................
PM2.5 .................................................
PM2.5 .................................................
PM2.5 .................................................
PM2.5 .................................................
PM2.5 .................................................
PM2.5 .................................................
PM2.5 .................................................
PM2.5 .................................................
PM2.5 .................................................
80
77
4.8
5.1
0.12
0.32
0.17
0.20
0.57
9.2
21
150
150
10
9.4
0.21
0.58
0.30
0.37
1.0
14
36
PM2.5 .................................................
...........................................................
3,400+ B
3,100+ B
6,500+ B
5,900+ B
a Dollars are rounded to two significant digits. The PM estimates represent benefits from the proposed rule across the contiguous United
States.
b Monetary benefits adjusted to account for growth in real GDP per capita between 1990 and the analysis year (2020 or 2030).
c Valuation of premature mortality based on long-term PM exposure assumes discounting over the SAB recommended 20 year segmented lag
structure described in the Regulatory Impact Analysis for the Final Clean Air Interstate Rule (March 2005). Results show 3 percent and 7 percent
discount rates consistent with EPA and OMB guidelines for preparing economic analyses (US EPA, 2000 and OMB, 2003).298
d Adult mortality based upon studies by Pope et al. 2002. Infant mortality based upon studies by Woodruff, Grillo, and Schoendorf, 1997.
e B represents the monetary value of health and welfare benefits not monetized. A detailed listing is provided in Table IX.E–1.
4. What Are the Significant Limitations
of the Benefit Analysis?
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Perhaps the most significant
limitation of this analysis is our
inability to quantify a number of
potentially significant benefit categories
associated with improvements in air
quality that would result from the
proposed standards. Most notably, we
are unable to estimate the benefits from
reduced air toxics exposures because
the available tools and methods to
assess mobile source air toxics risk at
the national scale are not adequate for
extrapolation to incidence estimations
or benefits assessment. We also do not
quantify ozone benefits due to the
magnitude of, and uncertainty
298 U.S. Environmental Protection Agency, 2000.
Guidelines for Preparing Economic Analyses.
www.yosemite1.epa.gov/ee/epa/eed/hsf/pages/
Guideline.html.
Office of Management and Budget, The Executive
Office of the President, 2003. Circular A–4. https://
www.whitehouse.gov/omb/circulars.
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associated with, the modeled changes in
ambient ozone associated with the
proposed gas can standards, despite net
benefits, when population weighted, in
the ozone design value metric observed
across the modeled domain (see Section
IV.C).
More generally, every benefit-cost
analysis examining the potential effects
of a change in environmental protection
requirements is limited to some extent
by data gaps, limitations in model
capabilities (such as geographic
coverage), and uncertainties in the
underlying scientific and economic
studies used to configure the benefit and
cost models. Deficiencies in the
scientific literature often result in the
inability to estimate quantitative
changes in health and environmental
effects, such as potential increases in
premature mortality associated with
increased exposure to carbon monoxide.
Deficiencies in the economics literature
often result in the inability to assign
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economic values even to those health
and environmental outcomes which can
be quantified. These general
uncertainties in the underlying
scientific and economics literature,
which can cause the valuations to be
higher or lower, are discussed in detail
in the RIA and its supporting references.
Key uncertainties that have a bearing on
the results of the benefit-cost analysis of
the proposed standards include the
following:
• The exclusion of potentially
significant and unquantified benefit
categories (such as health, odor, and
ecological benefits of reduction in air
toxics, ozone, and PM);
• Errors in measurement and
projection for variables such as
population growth;
• Uncertainties in the estimation of
future year emissions inventories and
air quality;
• Uncertainties associated with the
scaling of the PM results of the modeled
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benefits analysis to the proposed
standards, especially regarding the
assumption of similarity in geographic
distribution between emissions and
human populations and years of
analysis;
• Uncertainty in the estimated
relationships of health and welfare
effects to changes in pollutant
concentrations including the shape of
the C–R function, the size of the effect
estimates, and the relative toxicity of the
many components of the PM mixture;
• Uncertainties in exposure
estimation; and
• Uncertainties associated with the
effect of potential future actions to limit
emissions.
Despite these uncertainties, we
believe this benefit-cost analysis
provides a conservative estimate of the
expected economic benefits of the
proposed standards for cold temperature
vehicle control in future years because
of the exclusion of potentially
significant benefit categories.
Acknowledging benefits omissions and
uncertainties, we present a best estimate
of the total benefits based on our
interpretation of the best available
scientific literature and methods
supported by EPA’s technical peer
review panel, the Science Advisory
Board’s Health Effects Subcommittee
(SAB–HES). EPA has also worked to
address many of the comments made by
the National Academy of Sciences
(NAS) in a September 26, 2002 report on
its review of the Agency’s methodology
for analyzing the health benefits of
measures taken to reduce air pollution.
EPA addressed many of these comments
in the analysis of the final CAIR rule.299
The analysis of the proposed rule
incorporates this most recent work.
There is one category where new
studies suggest the possibility of
significant additional economic
benefits. Over the past several years,
EPA’s SAB has expressed the view that
there were not sufficient data to show a
separate ozone mortality effect, in
essence saying that any ozone benefits
are captured in the PM-related mortality
benefit estimates. However, in their
most recent advice, the SAB
recommended that EPA reconsider the
evidence on ozone-related mortality
based on the publication of several
recent analyses that found statistically
significant associations between ozone
and mortality. Based on these studies
and the recommendations from the
SAB, EPA sponsored three independent
299 See Chapter 4 of the Final Clean Air Interstate
Rule RIA (www.epa.gov/cair) for a discussion of
EPA’s ongoing efforts to address the NAS
recommendations in its regulatory analyses.
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meta-analyses of the ozone-mortality
epidemiology literature to inform a
determination on including this
important health endpoint. The studies
were peer-reviewed and printed in the
journal Epidemiology in July
2005.300 301 302
EPA is reviewing the body of
literature available on the association of
ozone exposure and premature
mortality. EPA’s second external review
draft of the Criteria Document for ozone
has concluded that there is strong
evidence that exposure to ozone has
been associated with premature
mortality.303 We are exploring ways of
appropriately characterizing the
premature mortality benefits of reducing
ozone and included an estimate in
recent analyses of the Clear Skies
legislation.304 We plan to include a
quantification of ozone mortality
benefits in future air pollution
rulemakings.
In contrast to the additional benefits
of the proposed standards discussed
above, it is also possible that this rule
will result in disbenefits in some areas
of the United States. The effects of
ozone and PM on radiative transfer in
the atmosphere can lead to effects of
uncertain magnitude and direction on
the penetration of ultraviolet light and
climate. Ground level ozone makes up
a small percentage of total atmospheric
ozone (including the stratospheric layer)
that attenuates penetration of
ultraviolet–b (UVb) radiation to the
ground. EPA’s past evaluation of the
information indicates that potential
disbenefits would be small, variable,
and with too many uncertainties to
attempt quantification of relatively
small changes in average ozone levels
over the course of a year.305 EPA’s most
recent provisional assessment of the
currently available information
300 Levy, J.I, Chemerynski, S.M., Sarnat, J.A. 2005.
Ozone Exposure and Mortality: An Empirical Bayes
Meta-Regression Analysis. Epidemiology. 16:458–
468.
301 Bell, M.L., Dominici, F., Samet, J.M. 2005. A
Meta-Analysis of Time-Series Studies of Ozone and
Mortality with Comparison to the National
Morbidity, Mortality, and Air Pollution Study.
Epidemiology. 16:436–445.
302 Ito, K., DeLeon, S.F., Lippmann, M. 2005.
Associations Between Ozone and Daily Mortality:
Analysis and Meta-Analysis. Epidemiology. 16:446–
457.
303 EPA, 2005. Air Quality Criteria for Ozone and
Related Photochemical Oxidants (Second External
Review Draft). August. https://cfpub.epa.gov/ncea/
cfm/recordisplay.cfm?deid=137307
304 For technical details about Clear Skies multipollutant analysis, see https://www.epa.gov/
airmarkets/mp/bmresults/
health_benefits_method.pdf
305 EPA, 2005. Air Quality Criteria for Ozone and
Related Photochemical Oxidants (First External
Review Draft). January. https://cfpub.epa.gov/ncea/
cfm/recordisplay.cfm?deid=114523
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indicates that potential but
unquantifiable benefits may also arise
from ozone-related attenuation of UVb
radiation.306 EPA believes that we are
unable to quantify any net climaterelated disbenefit or benefit associated
with the combined ozone and PM
reductions in this rule.
5. How Do the Benefits Compare to the
Costs of the Proposed Standards?
This proposed rule provides three
separate provisions that reduce air
toxics emissions from mobile sources:
cold temperature vehicle controls, an
emissions control program for gas cans,
and a control program limiting benzene
in gasoline. A full appreciation of the
overall economic consequences of these
provisions requires consideration of the
benefits and costs expected to result
from each standard, not just those that
could be expressed here in dollar terms.
As noted above, due to limitations in
data availability and analytical methods,
our benefits analysis only monetizes the
PM2.5-related benefits from direct PM
emission reductions associated with the
cold temperature standards. There are a
number of health and environmental
effects associated with the proposed
standards that we were unable to
quantify or monetize (see Table IX.E–1).
Table IX.E–4 contains the estimates of
monetized benefits of the proposed cold
temperature vehicle standards and
estimated social welfare costs for each
of the proposed control programs.307
The annual social welfare costs of all
provisions of this proposed rule are
described more fully in Section IX.F. It
should be noted that the estimated
social welfare costs for the vehicle
program contained in this table are for
2019. The 2019 vehicle program costs
are included for comparison purposes
only and are therefore not included in
the total 2020 social costs. There are no
compliance costs associated with the
vehicle program after 2019; as explained
elsewhere in this preamble, the vehicle
compliance costs are primarily R&D and
facilities costs that are expected to be
recovered by manufacturers over the
first ten years of the program.
The results in Table IX.E–4 suggest
that the 2020 monetized benefits of the
cold temperature vehicle standards are
greater than the expected social welfare
costs of that program in 2019.
Specifically, the annual benefits of the
306 EPA, 2005. Air Quality Criteria for Ozone and
Related Photochemical Oxidants (Second External
Review Draft). August. https://cfpub.epa.gov/ncea/
cfm/recordisplay.cfm?deid=137307
307 Social costs represent the welfare costs of the
rule to society. These social costs do not consider
transfer payments (such as taxes) that are simply
redistributions of wealth.
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program would be approximately $3,400
+ B million or $3,100 + B million
annually in 2020 (using a 3 percent and
7 percent discount rate in the benefits
analysis, respectively), compared to
estimated social welfare costs of
approximately $11 million in the last
year of the program (2019). These
benefits are expected to increase to
$6,500 + B million or $5,900 + B million
annually in 2030 (using a 3 percent and
7 percent discount rate in the benefits
analysis, respectively), even as the
social welfare costs of that program fall
to zero. Table IX.E–4 also presents the
costs of the other proposed rule
provisions: an emissions control
program for gas cans and a control
program limiting benzene in gasoline.
Though we are unable to present the
benefits associated with these two
programs, we note for informational
purposes that the benefits associated
with the proposed cold temperature
vehicle standards alone exceed the costs
of all three proposed rule provisions
combined.
TABLE IX.E–4.—SUMMARY OF ANNUAL BENEFITS OF THE PROPOSED COLD TEMPERATURE VEHICLE STANDARDS AND
COSTS OF ALL PROVISIONS OF THE PROPOSED STANDARDS a
[Millions of 2003 dollars]
Description
2020
2030
Estimated Social Welfare Costs b:
Proposed Cold Temperature Vehicle Standards ..................................................................................................
Proposed Gasoline Container Standards .............................................................................................................
Proposed Fuel Standards d ...................................................................................................................................
$11 c ............
32 ................
210 ..............
$0
39
250
Total ...............................................................................................................................................................
Fuel Savings ..........................................................................................................................................................
240 ..............
¥73 .............
290
¥82
Total Social Welfare Costs ............................................................................................................................
Total PM2.5-Related Health Benefits of the Proposed Cold Temperature Vehicle Standards e:
3 percent discount rate .........................................................................................................................................
7 percent discount rate .........................................................................................................................................
170 ..............
205
3,400 + B f ...
3,100 + B f ...
6,500 + B f
5,900 + B f
a All estimates are rounded to two significant digits and represent annualized benefits and costs anticipated for the years 2020 and 2030, except where noted. Totals may not sum due to rounding.
b Note that costs are the annual total costs of reducing all pollutants associated with each provision of the proposed MSAT control package.
Also note that while the cost analysis only utilizes a 7 percent discount rate to calculate annual costs, the benefits analysis uses both a 3 percent
and 7 percent discount rate to calculate annual benefits. Benefits reflect only direct PM reductions associated with the cold temperature vehicle
standards.
c These costs are for 2019; the vehicle program compliance costs terminate after 2019 and are included for illustrative purposes. They are not
included in the total social welfare cost sum for 2020.
d Our modeling for the total costs of the proposed gasoline benzene program included California gasoline, since it was completed before we
decided to propose that California gasoline not be covered by the program. California refineries comprise approximately 1 percent of these
2projected costs. For the final rule, we expect to exclude California refineries from the analysis.
e Valuation of premature mortality based on long-term PM exposure assumes discounting over the SAB recommended 20 year segmented lag
structure described in the Regulatory Impact Analysis for the Final Clean Air Interstate Rule (March 2005). Annual benefits analysis results reflect
the use of a 3 percent and 7 percent discount rate in the valuation of premature mortality and nonfatal myocardial infarctions, consistent with
EPA and OMB guidelines for preparing economic analyses (US EPA, 2000 and OMB, 2003).308
f Not all possible benefits or disbenefits are quantified and monetized in this analysis. B is the sum of all unquantified benefits and disbenefits.
Potential benefit categories that have not been quantified and monetized are listed in Table IX.E–1.
F. Economic Impact Analysis
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We prepared a draft Economic Impact
Analysis (EIA) to estimate the economic
impacts of the proposed emission
control program on the gas can, gasoline
fuel, and light-duty vehicle markets. In
this section we briefly describe the
Economic Impact Model (EIM) we
developed to estimate both the marketlevel changes in price and outputs for
affected markets and the social costs of
the program and their distribution
across affected economic sectors. We
also present the results of our analysis.
We estimate the net social costs of the
proposed program to be about $171.5
million in 2020. This estimate reflects
the estimated costs associated with the
308 U.S. Environmental Protection Agency, 2000.
Guidelines for Preparing Economic Analyses.
www.yosemite1.epa.gov/ee/epa/eed/hsf/pages/
Guideline.html.
Office of Management and Budget, The Executive
Office of the President, 2003. Circular A–4. https://
www.whitehouse.gov/omb/circulars.
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gasoline, gas can, and vehicle controls
and the expected fuel savings from
better evaporative controls on gas cans.
The results of the economic impact
modeling performed for the gasoline
fuel and gas can control programs
suggest that the social costs of those two
programs are expected to be about
$244.3 million in 2020 with consumers
of these products expected to bear about
60 percent of these costs. We estimate
fuel savings of about $72.8 million in
2020 that will accrue to consumers.
There are no social costs associated with
the vehicle program in 2020. These
estimates, and all costs presented in this
section, are in year 2003 dollars.
With regard to market level impacts in
2020, the maximum price increase for
gasoline fuel is expected to be about 0.1
percent (0.2 cents per gallon) for PADD
5. The price of gas cans is expected to
increase by about 1.8 percent ($0.20 per
can) in areas that already have gas can
requirements and about 32.5 percent
($1.52 per can) in areas that do not.
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Detailed descriptions of the EIM, the
model inputs, modeling results, and
several sensitivity analyses can be found
in Chapter 13 of the Regulatory Impact
Analysis prepared for this proposal.
1. What Is an Economic Impact
Analysis?
An Economic Impact Analysis (EIA) is
prepared to inform decision makers
about the potential economic
consequences of a regulatory action. The
analysis consists of estimating the social
costs of a regulatory program and the
distribution of these costs across
stakeholders. These estimated social
costs can then be compared with
estimated social benefits (as presented
in Section IX.E). As defined in EPA’s
Guidelines for Preparing Economic
Analyses, social costs are the value of
the goods and services lost by society
resulting from (a) the use of resources to
comply with and implement a
regulation and (b) reductions in
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output.309 In this analysis, social costs
are explored in two steps. In the market
analysis, we estimate how prices and
quantities of goods affected by the
proposed emission control program can
be expected to change once the program
goes into effect. In the economic welfare
analysis, we look at the total social costs
associated with the program and their
distribution across stakeholders.
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2. What Is the Economic Impact Model?
The Economic Impact Model (EIM) is
a behavioral model developed for this
proposal to estimate price and quantity
changes and total social costs associated
with the emission controls under
consideration. The EIM simulates how
producers and consumers of affected
products can be expected to respond to
an increase in production costs as a
result of the proposed emission control
program. In this EIM, compliance costs
are directly borne by producers of
affected goods. Depending on the
producers’ and consumers’ sensitivity to
price changes, producers may be able to
pass some or all of these compliance
costs on to the consumers of these goods
in the form of higher prices. Consumers
adjust their consumption of affected
goods in response to these price
changes. This information is passed
back to the producers in the form of
purchasing decisions. The EIM takes
these behavioral responses into account
to estimate new market equilibrium
quantities and prices for all modeled
sectors and the resulting distribution of
social costs across these stakeholders
(producers and consumers).
3. What Economic Sectors Are Included
in This Economic Impact Analysis?
There are three economic sectors
affected by the control programs
described in this proposal: gas cans,
gasoline fuel, and light-duty vehicles. In
this Economic Impact Analysis we
model only the impacts on the gas can
and gasoline fuel markets. We did not
model the impacts on the light-duty
vehicle market. This is because the
compliance costs for the proposed
vehicle program are expected to be very
small, less than $1 per vehicle and, even
if passed on entirely, are unlikely to
affect producer or consumer behavior.
Therefore, we do not expect these
proposed controls to affect the quantity
of vehicles produced or their prices. At
the same time, however, the light-duty
vehicle compliance costs are a cost to
society and should be included in the
309 EPA
Guidelines for Preparing Economic
Analyses, EPA 240–R–00–003, September 2000, p
113. A copy of this document can be found at
https://yosemite.epa.gov/ee/epa/eed.nsf/webpages/
Guidelines.html#download
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economic welfare analysis. We do this
by adding the vehicle program
engineering compliance cost estimates
to the estimated social costs of the
gasoline and gas can programs.
With regard to the gasoline fuel and
gas can markets, we consider only the
impacts on residential users of these
products. This means that we focus the
analysis on the use of these products for
personal transportation (gasoline fuel)
or residential lawns and garden care or
recreational uses (gas cans) and do not
consider how the costs of complying
with the proposed programs may affect
the production of goods and services
that use gasoline fuel or gas cans as
production inputs. We believe this
approach is reasonable because the
commercial share of the end-user
markets for both gasoline fuel and gas
cans is relatively small.310 311 In
addition, for most commercial users the
share of the cost of these products to
total production costs is also small (e.g.,
the cost of a gas can is only a very small
part of the total production costs for an
agricultural or construction firm).
Therefore, a price increase of the
magnitude anticipated for this control
program is not expected to have a
noticeable impact on prices or
quantities of goods produced using
these inputs (e.g., agricultural product
or buildings).
With regard to the gasoline fuel
analysis, it should be noted that this
Economic Impact Analysis does not
include California fuels in the market
analysis. California fuels are only
included, as a separate line item, in the
economic welfare analysis. California
currently has state-level controls that
address air toxics from gasoline. Any
actions that refiners may take to comply
with the federal program are expected to
be small and not affect market prices or
quantities in that state. However,
because the estimated fuel program
310 The U.S Department of Energy estimates that
about 92 percent of gasoline used in the United
States for transportation is used in light-duty
vehicles. About 6 percent is used for commercial or
industrial transportation, and the remaining 2
percent is used in recreational marine vessels. See
U.S Department of Energy, Energy Information
Administration, 2004. ‘‘Annual Energy Outlook
2004 with projections to 2025.’’ Last updated June
2, 2004. Table A–2 and Supplemental Table 34.
https://www.eia.doe.gov/oiaf/aeoref_tab.html.
311 A recent study by CARB (1999) found that 94
percent of portable fuel containers in California
were used by residential households California
Environmental Protection Agency, Air Resources
Board (CARB) 1999. See ‘‘Hearing Notice and Staff
Report, Initial Statement of Reasons for Proposed
Rule Making Public Hearing to Consider the
Adoption of Portable Fuel Container Spillage
Control Regulation.’’ Sacrament, CA: California
Environmental Protection Agency, Air Resources
Board (CARB). A copy of this document is available
at https://www.arb.ca.gov/regact/spillcon/isor.pdf
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15913
compliance costs include a small
compliance cost for California, and this
cost would be a cost to society, it is
necessary to include those costs in the
total economic welfare costs of the
proposal. This is done by including the
estimated engineering compliance costs
as a separate line item. Also, consistent
with the cost analysis, the economic
impact analysis does not distinguish
between reformulated and conventional
gasoline fuels.
The EIM models the economic
impacts on two gas can markets (states
that currently have requirements for gas
cans and those that do not), and four
gasoline fuel markets (PADDs 1+3,
PADD 2, PADD 4, PADD 5). The markets
included in this EIA are described in
more detail in Chapter 13 of the RIA for
this proposal.
In the EIM, the gasoline fuel and gas
can markets are not linked (there is no
feedback mechanism between the gas
can and gasoline fuel model segments).
This is because these two sectors
represent different aspects of fuel
consumption (fuel storage and fuel
production) and production and
consumption of one product is not
affected by the other. In other words, an
increase in the price of gas cans is not
expected to have an impact on the
production and supply of gasoline, and
vice versa. Production and consumption
of each of these products are the result
of other factors that have little crossover impacts (the need for fuel storage;
the need for personal transportation).
4. What Are the Key Features of the
Economic Impact Model?
A detailed description of the features
of the EIM and the data used in the
analysis is provided in Chapter 13 of the
RIA prepared for this rule. The model
methodology is firmly rooted in applied
microeconomic theory and was
developed following the methodology
set out in the OAQPS’s Economic
Analysis Resource Document.312
The EIM is a computer model
comprised of a series of spreadsheet
modules that simulate the supply and
demand characteristics of the markets
under consideration. The initial market
equilibrium conditions are shocked by
applying the compliance costs for the
control program to the supply side of
the markets (this is done by shifting the
relevant supply curves by the amount of
the compliance costs). The model
equations can be analytically solved for
312 U.S. Environmental Protection Agency, Office
of Air Quality Planning and Standards, Innovative
Strategies and Economics Group, OAQPS Economic
Analysis Resource Document, April 1999. A copy
of this document can be found at https://www.
epa.gov/ttn/ecas/econdata/Rmanual2/
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equilibrium prices and quantities for the
markets with the regulatory program
and these new prices and quantities are
used to estimate the social costs of the
model and how those costs are shared
among affected markets.
The EIM is a partial equilibrium,
intermediate-run model that assumes
perfect competition in the relevant
markets. As explained in EPA’s
Guidelines for Preparing Economic
Analyses, ‘‘partial equilibrium’’ means
that the model considers markets in
isolation and that conditions in other
markets are assumed either to be
unaffected by a policy or unimportant
for social cost estimation.313 The use of
the intermediate run means that some
factors of production are fixed and some
are variable. In very short analyses, all
factors of production would be assumed
to be fixed, leaving the producers with
no means to respond to the increased
production costs associated with the
regulation (e.g., they cannot adjust labor
or capital inputs). Under this time
horizon, the costs of the regulation fall
entirely on the producer. In the long
run, all factors of production are
variable and producers can adjust
production in response to cost changes
imposed by the regulation (e.g., using a
different labor/capital mix). In the
intermediate run there is some resource
immobility which may cause producers
to suffer producer surplus losses, but
they can also pass some of the
compliance costs to consumers.
The perfect competition assumption
is widely accepted economic practice
for this type of analysis, and only in rare
cases are other approaches used.314 It
should be noted that the perfect
competition assumption is not primarily
about the number of firms in a market.
It is about how the market operates: the
nature of the competition among firms.
Indicators that allow us to assume
perfect competition include absence of
barriers to entry, absence of strategic
behavior among firms in the market, and
product differentiation.
With regard to the gasoline fuel
market, the Federal Trade Commission
(FTC) has developed an approach to
ensure competitiveness in gasoline fuel
markets. It reviews oil company mergers
and frequently requires divestiture of
refineries, terminals, and gas stations to
maintain a minimum level of
competition. This is discussed in more
313 EPA Guidelines for Preparing Economic
Analyses, EPA 240–R–00–003, September 2000, p.
125–6.
314 See, for example, EPA Guidelines for
Preparing Economic Analyses, EPA 240–R–00–003,
September 2000, p 126.
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detail in the industry profile prepared
for this proposal.315
With regard to the gas can market, the
small number of firms in the market is
offset by several features of this market.
Because gas cans are compact and
lightweight, they are easy to transport
far from their place of manufacture. This
means that production is not limited to
local producers. Although they vary by
size and material, consumers are likely
to view all gas cans as good substitutes
for one another. Because the products
are similar enough to be considered
homogeneous (e.g., perfectly
substitutable), consumers can shift their
purchases from one manufacturer to
another. There are only minimal
technical barriers to entry that would
prevent new firms from freely entering
the market, since manufacturing is
based on well-known plastic processing
methods. In addition, there is significant
excess capacity, enabling competitors to
respond quickly to changes in price.
Excess production capacity in the
general container manufacturing market
also means that manufacturers could
potentially switch their product lines to
compete in this segment of the market,
often without a significant investment.
In addition, there is no evidence of high
levels of strategic behavior in the price
and quantity decisions of the firms.
Finally, it should be noted that
contestable market theory asserts that
oligopolies and even monopolies will
behave very much like firms in a
competitive market if manufacturers
have extra production capacity and this
capacity could allow them to enter the
market costlessly (i.e., there are no sunk
costs associated with this kind of market
entry or exit).316 As a result of these
conditions, producers and consumers in
the gas can market take the market price
as given when making their production
and consumption choices. For all these
reasons, the market can be modeled as
a competitive market even though the
number of producers is small.
5. What Are the Key Model Inputs?
Key model inputs for the EIM are the
behavioral parameters, compliance costs
315 Section 3 Industry Organization,
‘‘Characterizing Gasoline Markets: a Profile,’’ Final
Report, prepared for EPA by RTI, August 2005.
316 A monopoly or firms in oligopoly may not
behave as neoclassical economic theories of the
firm predict because they may be concerned about
new entrants to the market. If super-normal profits
are earned, potential competitors may enter the
market. To respond to this treat, existing firm(s) in
the market will keep prices and output at a level
where only normal profits are made, setting price
and output levels at or close to the competitive
price and output. See Chapter 13 of the RIA for
more information, Section 13.2.3.
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estimates, and market equilibrium
quantities and prices.
The EIM is a behavioral model. The
estimated social costs of this emission
control program are a function of the
ways in which producers and
consumers of the gas cans and gasoline
fuel affected by the standards change
their behavior in response to the costs
incurred in complying with the
standards. These behavioral responses
are incorporated in the EIM through the
price elasticity of supply and demand
(reflected in the slope of the supply and
demand curves), which measure the
price sensitivity of consumers and
producers. The price elasticites used in
this analysis are described in Chapter 13
of the RIA. The gasoline elasticites were
obtained from the literature and are
¥0.2 for demand and 0.2 for supply.
This means that both the quantity
supplied and demanded are expected to
be fairly insensitive to price changes
and that increases in prices are not
expected to cause sales to fall or
production to increase by very much.
Because we were unable to find
published supply and demand
elasticities for the gas can market, we
estimated these parameters using the
procedures described in Chapter 13 of
the RIA. This approach yielded a
demand elasticity of ¥0.01 and a
supply elasticity of 1.5. The estimated
demand elasticity is nearly perfectly
inelastic (equal to zero), which means
that changes in price are expected to
have very little effect on the quantity of
gas cans demanded. However, supply is
fairly elastic, meaning producers are
expected to respond to a change in
price. Therefore, consumers are
expected to bear more of the burden of
gas can regulatory control costs than
producers.
Initial market equilibrium conditions
are simulated using the same current
year sales quantities and growth rates
used in the engineering cost analysis.
The initial equilibrium prices for gas
can and gasoline fuel were obtained
from industry sources and published
government data. The initial
equilibrium market conditions are
shocked by applying the engineering
compliance cost estimates described in
earlier in this section. Although both the
gas can and gasoline fuel markets are
competitive markets, the model is
shocked by applying the sum of variable
and fixed costs. Two sets of compliance
costs are used in the gas can market
analysis, reflecting states with existing
controls and states without existing
controls. The compliance costs used to
shock the gasoline fuel market are based
on an average total cost (variable +
fixed) analysis. An explanation for this
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approach can be found in Section
13.2.4.1 of the RIA prepared for this
proposal. These gasoline fuel
compliance costs differ across PADDs
but are the same across years. Because
California already has existing gasoline
fuel controls, fuel volumes for that state
are not included in the market analysis.
However, because it may be necessary
for refiners to adjust their production to
comply with the new federal standards,
California fuel controls are included in
the economic welfare analysis.
Additional costs that need to be
considered in the EIM are the savings
associated with the gas can controls and
the costs of the light-duty vehicle
controls. The proposed gas can controls
are expected to reduce evaporative
emissions from fuel storage, leading to
fuel savings for users of these
containers. These fuel savings are not
included in the market analysis for this
economic impact analysis because these
savings are not expected to affect
consumer decisions with respect to the
purchase of new containers. Fuel
savings are included in the social cost
analysis, however, because they are a
savings that accrues to society. The
estimated fuel savings are added to the
estimated social costs as a separate line
item. As noted above, the economic
impacts of the light-duty vehicle
controls are not modeled in the EIM.
Instead, the estimated engineering
compliance costs are used as a proxy,
and are also added into the estimated
social costs as a separate line item.
The EIM relies on the estimated
compliance costs for the gas can and
gasoline fuel programs described
elsewhere in this preamble. Thus, the
EIM reflects cost savings associated with
ABT or other flexibility programs to the
extent they are included in the
estimated compliance costs.
6. What Are the Results of the Economic
Impact Modeling?
Using the model and data described
above, we estimated the economic
impacts of the proposed emission
control program. The results of our
analysis are summarized in this section.
Detailed results for all years are
included in the appendices to Chapter
13 of the RIA. Also included as an
appendix to that chapter are sensitivity
analyses for several key inputs.
Market Impact Analysis. Market
impacts are the estimated changes in the
quantity of affected goods produced and
their prices. As explained above, we
estimated market impacts for only
gasoline fuel and gas cans, and
California fuel is not included in the
market analysis for PADD 5. The
estimated market impacts are presented
in Table IX.F–1. In this table the market
results for gasoline are presented for
only 2015 because the compliance costs
for the gasoline fuel program are
constant for all years and therefore the
results of the market analysis are the
same for all years.317 The market results
for gas cans are presented for 2009 and
2015, reflecting the changes in
estimated compliance costs due to
amortization of fixed costs over the first
five years of the program. After 2013 the
compliance costs remain constant for all
future years.318
With regard to the gasoline fuel
program, the market impacts are
expected to be small, on average. The
price of gasoline fuel is expected to
increase by about 0.15 percent or less,
depending on PADD. The expected
reduction in quantity of fuel produced
is expected to be less than 0.03 percent.
The market impacts for the gas can
program are expected to be more
significant. In 2009, the first year of the
gas can program, the model predicts a
price increase of about 7 percent for gas
cans in states that are currently have
regulations for gas cans and about 57
percent for those that do not. Even with
these larger price increases, however,
the quantity produced is not expected to
decrease by very much, less than 0.6
percent. These percent price increases
and quantity decreases much smaller
after the first five years. In 2015, the
estimated gas can price increase is
expected to be less than 2 percent for
states that currently regulate gas cans
and about 32.5 percent for states
without such regulations. The quantity
produced is expected to decrease by less
than 0.4 percent. These changes are
expected to remain constant for future
years, even though the absolute
quantities produced are expected to
increase somewhat.
TABLE IX.F–1.—SUMMARY OF MARKET IMPACTS
Change in price
Engineering
cost per unit
Market
Absolute
Percent
Change in quantity
Absolute
Percent
2009
Gasoline Fuel:
PADD 1 & 3.
PADD 2 .....................................................................................
PADD 4.
PADD 5 (w/out CA).
N/A (gasoline fuel control program begins in 2011)
$/can
Gas Cans:
States with existing programs ..................................................
States without existing programs .............................................
$0.77 ...........
$2.70 ...........
$0.76 ...........
$2.68 ...........
Thousand Cans
6.9% ............
57.4% ..........
¥6.8 ...........
¥88.5 .........
¥0.07%
¥0.57%
2015
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¢/gallon
Gasoline Fuel:
PADD 1 & 3 ..............................................................................
PADD 2 .....................................................................................
317 The number of gallons of gasoline fuel
produced is expected to decrease in future years,
but the percent decrease is expected to remain the
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0.049¢ .........
0.202¢ .........
0.03¢ ...........
0.11¢ ...........
same; this is due to the growth in fuel consumption
generally.
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Million Gallons
0.02% ..........
0.07% ..........
¥3.1 ...........
¥6.9 ...........
¥0.004%
¥0.015%
318 The number of gas cans produced is expected
to decrease in future years, but the percent decrease
is expected to remain the same; this is due to the
growth in gas can production generally.
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TABLE IX.F–1.—SUMMARY OF MARKET IMPACTS—Continued
Change in price
Change in quantity
Engineering
cost per unit
Market
PADD 4 .....................................................................................
PADD 5 (w/out CA) ..................................................................
Absolute
Percent
Absolute
0.358¢ .........
0.391¢ .........
0.19¢ ...........
0.21¢ ...........
0.12% ..........
0.13% ..........
¥1.4 ...........
¥2.5 ...........
$/can
Gas Cans:
States with existing programs ..................................................
States without existing programs .............................................
Economic Welfare Analysis. In the
economic welfare analysis we look at
the costs to society of the proposed
program in terms of losses to consumer
and producer surplus. These surplus
losses are combined with the estimated
vehicle compliance costs, fuel savings,
and government revenue losses to
estimate the net economic welfare
impacts of the proposed program.
Estimated annual net social costs for
selected years are presented in Table
IX–F–2. Initially, the estimated social
costs of the program are relatively small
and are attributable to the gas can
program, which begins in 2009, and the
vehicle program, which begins in 2010.
For 2009 and 2010 the estimated social
costs are less than $40 million. In 2011
the estimated social costs increase to
$215 million, reflecting the beginning of
the gasoline fuel program. In subsequent
years, estimated social costs increase
due to growth. However, they decrease
in 2014, to $169 million, when the gas
can fixed costs are fully recovered and
in 2020, to $171.5 million, when the
vehicle program compliance costs are
terminated.
$0.21 ...........
$1.53 ...........
$0.20 ...........
$1.52 ...........
Percent
¥0.025%
¥0.026%
Thousand Cans
1.9% ............
32.5% ..........
¥2.1 ...........
¥56.4 .........
¥0.02%
¥0.32%
Table IX.F–3 contains more detailed
TABLE IX.F–2.—NET SOCIAL COSTS
ESTIMATES FOR THE PROPOSED estimated social costs for 2009, when
the gas can program begins, 2011, when
PROGRAM
[2009 to 2035—2003$, $million]
Total social
costs
(includes fuel
savings)
Year
2009 ......................................
2010 ......................................
2011 ......................................
2012 ......................................
2013 ......................................
2014 ......................................
2015 ......................................
2016 ......................................
2017 ......................................
2018 ......................................
2019 ......................................
2020 ......................................
2021 ......................................
2022 ......................................
2023 ......................................
2024 ......................................
2025 ......................................
2026 ......................................
2027 ......................................
2028 ......................................
2029 ......................................
2030 ......................................
2031 ......................................
2032 ......................................
2033 ......................................
2034 ......................................
2035 ......................................
NPV at 3% ............................
NPV at 7% ............................
$38.4
39.2
215.0
208.6
202.2
169.3
171.6
173.6
175.5
177.3
179.7
171.5
174.2
176.9
179.9
183.3
186.8
190.3
193.9
197.6
201.3
205.2
209.1
213.1
217.2
221.4
225.7
2,937.3
1,633.0
the gasoline fuel program begins, and
2015, when the gas can fixed costs are
fully recovered. The vehicle program
applies from 2010 through 2019.
According to these results, consumers
are expected to bear approximately 99
percent of the cost of the gas can
program. This reflects the inelastic price
elasticity on the demand side of the
market and the elastic price elasticity on
the supply side. The burden of the
gasoline fuel program is expected to be
shared more evenly, with 54.5 percent
expected to be borne by consumers and
45.5 percent expected to be borne by
producers. In all years, the estimated
loss to consumer welfare will be offset
somewhat by the fuel savings associated
with gas cans. Beginning at about $11
million per year, these savings increase
to about $70 million by 2015 as
compliant gas cans are phased in. These
savings accrue for the life of the gas
cans.
TABLE IX.F–3.—SUMMARY OF NET SOCIAL COSTS ESTIMATES ASSOCIATED WITH PRIMARY PROGRAM
[2009, 2011, and 2015—2003$, $million]
Change in
consumer
surplus
Market
Change in
producer
surplus
Total
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2009
Gasoline U.S.:
PADD 1 & 3
PADD 2
N/A (gasoline fuel control program begins in
2011)
PADD 4.
PADD 5 (w/out CA).
Gas Cans U.S. ....................................................................................................................................
States with existing programs .............................................................................................................
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-$48.7 ..........
(99.3%) ........
-$7.5 ............
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-$0.3 ............
(0.7%)
-$0.1.
-$49.0
Federal Register / Vol. 71, No. 60 / Wednesday, March 29, 2006 / Proposed Rules
15917
TABLE IX.F–3.—SUMMARY OF NET SOCIAL COSTS ESTIMATES ASSOCIATED WITH PRIMARY PROGRAM—Continued
[2009, 2011, and 2015—2003$, $million]
Market
Change in
consumer
surplus
Change in
producer
surplus
States without existing programs ........................................................................................................
-$41.2 ..........
-$0.3.
Subtotal .................................................................................................................................
-48.7 ............
(99.3%) ........
-0.3 ..............
(1%) ............
-$49.0
Fuel Savings .......................................................................................................................................
Vehicle Program .................................................................................................................................
California fuel a ....................................................................................................................................
.....................
.....................
.....................
.....................
.....................
.....................
$10.6
$0
$0
Total ...............................................................................................................................
.....................
.....................
-$38.4
-$100.3 ........
-$21.6 ..........
-$49.1 ..........
-$10.2 ..........
-$19.4 ..........
-$50.7 ..........
(99.4%) ........
-$7.8 ............
-$42.9 ..........
-$83.6 ..........
-$18.0
-$40.9
-$8.5
-$16.2
-$0.3 ............
(0.7%)
-$0.1
-$0.3.
-$183.9
Subtotal .................................................................................................................................
-$150.9 ........
(64.3%) ........
-$83.9 ..........
(35.7%)
-$234.8
Fuel Savings .......................................................................................................................................
Vehicle Program .................................................................................................................................
California fuel a ....................................................................................................................................
Total ...............................................................................................................................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
.....................
$33.3
-$11.8
-$1.7
$215.0
-$107.1 ........
(54.5%) ........
-$23.1 ..........
-$52.4 ..........
-$10.9 ..........
-$20.7 ..........
-$28.5 ..........
(99.3%) ........
-$2.3 ............
-$26.3 ..........
-$135.7 ........
(60.3%) ........
.....................
.....................
.....................
.....................
-$89.4 ..........
(45.5%)
-$19.3
-$43.7
-$9.1
-$17.3
-$0.2 ............
(0.7%)
$0.0
-$0.2
-$89.5 ..........
(39.7%)
.....................
.....................
.....................
.....................
-$196.5
Total
2011
Gasoline U.S. ......................................................................................................................................
PADD 1 & 3 ........................................................................................................................................
PADD 2 ...............................................................................................................................................
PADD 4 ...............................................................................................................................................
PADD 5 9w/out CA) ............................................................................................................................
Gas Cans U.S. ....................................................................................................................................
States with existing programs .............................................................................................................
States without existing programs ........................................................................................................
-$51.0
2015
Gasoline U.S. ......................................................................................................................................
PADD 1 & 3 ........................................................................................................................................
PADD 2 ...............................................................................................................................................
PADD 4 ...............................................................................................................................................
PADD 5 (w/out CA) .............................................................................................................................
Gas Cans U.S. ....................................................................................................................................
States with existing programs .............................................................................................................
States without existing programs ........................................................................................................
Subtotal .................................................................................................................................
Fuel Savings .......................................................................................................................................
Vehicle Program .................................................................................................................................
California fuel a ....................................................................................................................................
Total ...............................................................................................................................
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a California
-$225.2
$68.3
$12.9
-$1.8
$171.6
fuel costs are considered separately. See Section 13.1.3 of the RIA.
The present value of net social costs
(discounted back to 2005) of the
proposed standards through 2035,
contained in Table IX–F–2, is estimated
to be $2.9 billion (2003$). This present
value is calculated using a social
discount rate of 3 percent and the
stream of economic welfare costs from
2009 through 2035. We also performed
an analysis using a 7 percent social
discount rate.319 Using that discount
319 EPA has historically presented the present
value of cost and benefits estimates using both a 3
percent and a 7 percent social discount. The 3
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rate, the present value of the net social
costs through 2035 is estimated to be
$1.6 billion (2003$).
X. Alternative Program Options
We considered several options for
fuels, vehicles, and gas cans in
developing this proposal.
percent rate represents a demand-side approach and
reflects the time preference of consumption (the
rate at which society is willing to trade current
consumption for future consumption). The 7
percent rate is a cost-side approach and reflects the
shadow price of capital.
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A. Fuels
We considered a wide range of control
strategies for gasoline to reduce toxic
emissions. Among the options
considered are a toxics performance
standard, varying levels of benzene
control, approaches for controlling other
MSATs in addition to benzene, and
lower sulfur and RVP for VOC control.
The discussion of these options is
provided in section VII.
In addition, we request comment on
the following specific concepts relating
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to the proposed ABT and compliance
assurance provisions.
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1. Alternative Compliance Assurance
Provisions
The design of the proposed ABT
program is based on other recent fuel
programs (primarily gasoline and diesel
sulfur), but with fewer restrictions. The
proposed program includes nationwide
trading, does not include an upper limit
on benzene, and combines all fuel into
a single pool for credit accounting
purposes. The compliance assurance
mechanisms for the proposed ABT
program are also based on previous
recent fuel programs (including
reformulated gasoline and gasoline and
diesel sulfur) which in turn were
developed based on the experiences in
enforcing past fuel programs. At the
same time there are other programs with
different ABT and corresponding
compliance assurance provisions that
could serve as models for this benzene
proposal, such as the Acid Rain
Program.
An overarching concern that today’s
proposal attempts to address, and that
any alternative program also would
have to address, is that EPA does not
have the resources to audit a substantial
number of refineries each year, and
certainly not every refinery. Thus, we
must devise a credit program whose
enforcement integrity does not depend
on EPA conducting annual audits of
many or most refiners to determine the
validity of credits generated, transferred,
banked and used.
The program as proposed would
provide a great deal of flexibility to
refiners in complying with the
standards, but balances this flexibility
with provisions to ensure the standard’s
enforceability. This program would also
provide incentives for refiners and
importers to ensure the validity of any
credits they obtain, through the
provisions that hold the buyer of invalid
credits liable for any resulting violation
of the standard. We summarize the most
important of these provisions here:
• Credit life would be limited to 5
years. This is intended to provide
reasonable assurance that EPA will have
the opportunity to review the
appropriate records to verify
compliance, regardless of personnel
changes, whether existing refiners and
importers are bought, sold, merged, or
go out of business, and whether new
refiners and importers are created;
• Records would be required to be
retained for the life of the credits to
allow for EPA to enforce the benzene
content standard through random
audits;
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• We propose that credits be limited
in the number of trades that would be
allowed and are requesting comment on
the range from 2 to 4 trades. (We will
establish an appropriate number of
permissible trades in the final rule.)
Such a limitation would be intended to
allow EPA to have a reasonable chance
of verifying the validity of credits that
are traded;
• Both the buyer and seller of the
credits would be potentially liable
should credits be found to be invalid, in
order to allow EPA to maintain the
environmental benefits of the program
should the credit seller no longer be in
business; and
• Purchasers of credits would need to
be potential credit users, and so would
be refiners or importers. Our
experiences during the gasoline lead
phase-down program in the 1980s,
where brokers and others were allowed
to take title to lead credits, raised
enforcement problems severe enough to
call the program’s validity into question.
These problems have not arisen for
more recent programs, where credit
purchasers must be credit users.
We request comment on these
provisions as a whole and individually.
In addition, we note that the proposed
benzene program is different from the
other recent fuel programs in several
key respects that may provide
opportunities to design the ABT
program and corresponding compliance
assurance mechanisms differently. For
example, the proposed program would
not have an upper limit on the pergallon benzene concentration that
would otherwise force all refiners to
ultimately comply with the standard
through actual physical refinery
changes. Since this proposed program
would allow some degree of variation in
benzene levels to continue indefinitely,
additional flexibility in how credits are
handled may be desirable. Thus, we
specifically request comment on the
following alternate ABT program
elements.
As mentioned above, EPA could not,
with its limited resources, conduct
annual audits of all refiners (and
possibly other parties, as discussed
below). With regard to any potential
alternative ABT program elements,
including those discussed below, we
request detailed ideas about a potential
auditing process that would be
sufficiently robust to assure the validity
of credits generated, used, banked or
traded, including how such audits
might be self-funded.
Credit Life
EPA notes that a system that limits
credit life may, under certain
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circumstances, depress the market price
of credits and create less incentive for
benzene reductions early in the
program. EPA therefore requests
comment on whether the credit life
should be limited or whether unlimited
banking should be encouraged through
having credits with unlimited life or
longer life. We also seek comment on
how a program with unlimited credit
life could be successfully enforced. For
example, EPA audits for refinery
compliance with fuel standard and
credit requirements normally include
review of refinery production, testing
and business records. EPA seeks
comment on whether these audits could
be effectively conducted to review the
validity of credits that were generated
more than five years previously and
whether audits could be effectively
concluded during the first five years of
a credit’s life.
EPA also seeks comment on the
appropriate consequences if EPA was
unable to verify credit validity, the
criteria for identifying credits as being
invalid, and whether EPA should have
the burden of proving credits were
invalid or whether the credit generator
(or the credit user) should have the
burden of proving that credits were
valid. See Hazardous Waste Treatment
Council v. EPA, 886 F. 2d 355, 367–68
(D.C. Cir. 1990) ( relating to
circumstances when the burden of proof
may permissibly shift to a regulated
entity). EPA also seeks comment on
mechanisms that would allow
companies to verify the validity of
credits they generate without the need
for EPA audits. Thus, EPA seeks
comment on whether audits conducted
by independent auditors could be a
reliable indicator of credit validity, and
if so, the necessary qualifications of the
auditor, the criteria for auditor
independence, how these qualifications
and independence should be
established, whether the audit should
review records of all company fuels
activities related to credit creation or
only a random portion of these records,
the appropriate timing requirements for
these audits, and the nature and timing
of reports. EPA seeks comment on the
enforcement implications of the Clean
Air Act’s five-year statute of limitations
if credits with a life longer than five
years were allowed.
Record Retention
We also seek comment on whether a
program with unlimited credit life
would need to require that the
associated records be retained
indefinitely until a credit was used.
(The use of credits for which no records
exist could result in their being declared
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null and void since credit validity could
not be established.) We seek comment
as to whether record-keeping and EPA
audits involving activities occurring
more than five years in the past could
create any issues regarding statutes of
limitations. Also, in general, we request
comment on provisions that could
address the fact that the farther back in
time an event occurred, the more
difficult it becomes for EPA to conduct
an effective audit (due to factors such as
mergers, acquisitions, and turnover of
personnel). EPA seeks comment on
whether the Clean Air Act’s five-year
statute of limitations would adversely
impact EPA’s ability to enforce a
requirement to keep records longer than
five years.
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Number of Times Credits May Be
Traded
As described earlier in this preamble,
EPA is requesting comment on allowing
credits to be traded between 2 and 4
times. In particular, EPA seeks comment
on any specific benefits to regulated
parties or to the credit market generally
if a number of trades in this range were
allowed; on requirements that should be
included to ensure the validity of
credits that have been transferred
multiple times; on procedures for
identifying which credits have been
transferred if the credit transferor is
found to have had in its possession both
valid and invalid credits; and on
appropriate consequences to the
generator and/or transferor of invalid
credits. In addition, EPA seeks comment
on mechanisms that would allow
companies to establish the validity of
credits they have purchased without the
need for EPA audits. Thus, EPA requests
comment on whether companies that
obtain credits that have previously been
purchased should be required to
establish their validity through reports
of independent audits of the creditcreation activities of the company that
created the credits and of the credit
activities of any intermediary entities to
which the credits had been transferred.
Case-By-Case Relaxation of Compliance
Restrictions
In addition to seeking comment on
general modifications discussed above
to the proposed provisions, we also
request comment on allowing regulated
entities to petition for case-by-case
relaxation of specific provisions in
special cases. For example, such a
provision might allow a refiner to
petition EPA to allow a specific group
of credits to be traded one or more
additional times than the final rule
ultimately allows. Petitioners might also
be allowed to request an extension of
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the five year limit on credit life. EPA
seeks comment on whether and how
such an extension might affect the
ability to enforce the benzene content
standard, including impacts from the
statute of limitations. Such an exception
might have important implications for
enforcement, record-keeping, and
emissions, which would have to be
adequately addressed. EPA seeks
comment on the nature of
documentation that would be required
in such a petition and criteria that might
be used to make a determination
regarding approval of such a petition.
EPA also seeks comment on the extent
to which any such ABT flexibility
provisions would be used, and what the
benzene content, enforcement, liquidity,
and other implications might be.
Ownership of Benzene Credits
The potential modifications of the
proposed program on which we request
comment may be able to be
accomplished relatively easily within
the bounds of the proposed program.
Another concept, allowing traders and
other entities to take title to credits,
might best be accomplished by moving
to an entirely different type of credit
program, since it might require a set of
other related changes in order to
function effectively. For example, it may
be possible to design the benzene
trading program and related compliance
assurance provisions in a manner that
would allow benzene credits to be
traded on the open market like many
other commodities and not unlike the
way SO2 credits are traded under the
Acid Rain Program, or how carbon
credits are traded through the voluntary
trading program established by the
Chicago Climate Exchange. We next
discuss such an alternate credit
program.
The proposed restriction of benzene
credit use to refiners and importers does
not provide an opportunity for other
entities to participate in this credit
market by taking title to credits.320 The
inability of traders to take actual title to
credits may reduce the ability of the
market to function in certain ways
including, for example, to hedge against
risk effectively or to aggregate small
holdings into larger blocks for sale. This
might be avoided if the program
provided for benzene credits to be
owned, and for entities other than
320 In the proposed program non-refiners would
be allowed to facilitate, or broker, credit
transactions between refiners or importers. Thus, a
refiner (or importer) that needed to purchase credits
could contract with a broker to identify refiners or
importers that have credits to sell.
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15919
refiners and importers to obtain, hold,
and transfer them.
EPA requests comment on any
specific benefits to regulated parties or
to the credit market generally if nonrefiners were allowed to take title to
credits. EPA also requests comments on
any situations that occurred under other
motor vehicle fuels credit programs
where the absence of non-refiner credit
owners created difficulties or problems
in regulated parties being able to
transfer or obtain credits. EPA seeks
comment on how the benzene credit
program could be reliably enforced if
non-refiners were allowed to own
credits. Thus, EPA seeks comment on
the qualifications that should be
required for a company to be a nonrefiner credit owner, and how these
qualifications should be established; on
any registration, record keeping,
reporting, independent audit and
independent attestation requirements
that should be imposed on non-refiner
owners of credits; and on the nature of
liability that should attach to nonrefiner owners of credits that were
found to have transferred invalid
credits.
We expect that such a program would
require that all refiners and importers
have their credits (and therefore
compliance) verified each year. Given
the resource needs for EPA to undertake
such verifications, we would expect to
require refiners to utilize independent
auditors, sufficient for the auditor to
make a verified audit finding that the
company’s assertions regarding credit
creation are correct. We believe that
verification of credits in this manner
would require a complete audit of the
gasoline production and testing records
related to the benzene content and
volume of gasoline produced or
imported, including reviews and
reconciliation of all batch information.
The audit also would also have to
include sufficient review of records of
product sales to verify the completeness
of the gasoline production records. The
independent auditor performing such an
audit would have to be qualified to
understand and review the records of
gasoline production and testing
generated at a refinery, or the
importation and testing records
associated with imported gasoline. To
the extent that gasoline testing was
conducted by independent laboratories,
the credit audit would have to include
the activities of the independent
laboratory to make an audit finding of
the validity of the laboratory test results.
EPA would then continue to have the
ability to perform spot audits.
EPA seeks comment on whether the
regulations should require that these
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independent audits must be conducted
by an independent audit organization
that is funded by an industry
consortium, rather than by audit firms
individually retained by refiners/
importers. The industry consortium
would submit to EPA for approval: the
consortium organization; the
qualifications of the individual auditors;
the general audit plans, and any audit
plans that are specific to an individual
company. The audit organization would
submit audit reports to EPA and to the
companies that were the subject of their
audits.
The refiners and importers would
then assign a unique serial number to
each credit containing key information
including the entity’s registration
number, the year, and the credit
number. These entities would then
report this information to EPA as a part
of their annual compliance report.
Credits properly generated under such a
program could then be traded freely
until they were used. If an audit
determined that some credits were
improperly generated, a mechanism
would be required to decide which
credits were considered to be valid and
which invalid.
Given EPA’s resource constraints,
EPA seeks comment on a mechanism
that would allow refiners and importers,
and non-refiner owners of credits (if
allowed) to conduct this detailed
tracking of individual credits, with
reconciliation of the reports of all
parties transferring, obtaining, or
holding credits. Thus, EPA seeks
comment on whether the regulations
should include an option whereby
companies that wish to sell, purchase or
hold verified credits would fund an
independent organization that would
function as the clearinghouse of
benzene credits. EPA also seeks
comment on how such an independent
organization option should be
structured: What would be the
qualifications of the organization and
how would they be established; how
would the method of operations of the
organization be established and
approved by EPA; what reporting by
companies to the organization would be
required, and what reporting to EPA by
the organization would be required; and
how would the organization establish
the validity of credits that are the
subject of reports from companies.
In addition, as in past programs, if
credits were later found to be
improperly created, the party that
generated the invalid credits and the
party that used the invalid credits
would be subject to EPA enforcement.
The party using the invalid credits
would be required to remove the invalid
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credits from its compliance calculations.
If this recalculation resulted in a
violation of the benzene standard, the
party would be subject to an
enforcement action for this violation,
regardless of whether the invalid credits
were purchased in good faith (although
the party may be permitted to remedy
such violations through the subsequent
purchase of valid credits). This is
intended to maintain the environmental
benefits of the program and to
encourage self-policing by the industry
of the validity of the credits they use for
compliance. However, in this situation
EPA would look first to the generator of
the invalid credits to remedy the
shortfall. If this generator could make
up any credit deficit, EPA normally
would defer enforcement against the
user or intermediary transferor of
invalid credits.
2. Alternative ABT Options
EPA seeks comment on whether the
regulations should create two options
for benzene credits: one that is based on
the credit enforcement provisions
contained in the proposed fuels
program, resulting in credits with more
limited credit life that must be
transferred from the credit generator to
the credit user; and ‘‘verified’’ benzene
credits that have a longer credit life and
that can be owned by companies other
than refiners/importers. Under this
approach, benzene credits could be
‘‘verified’’ if certain conditions are met.
First, the credit generator would need to
participate in an audit consortium (as
described above) and the credits would
need to be verified through an audit
conducted by this organization. Second,
the credit generator and any other
company that took title to or used these
credits would need to participate in a
benzene credit clearing house (as
described above). In this way,
companies that wished to generate
benzene credits with longer life and
broader ownership options could do so,
but also would bear at least part of the
expense associated with establishing the
validity and tracking the movements of
this class of credits. At the same time,
companies that wished to generate and
transfer credits in the traditional
manner, would not bear these extra
expenses.
EPA also seeks comment on an
approach that would allow refiners and
importers, and non-refiner owners of
credits (if allowed), to establish a
private clearing house to conduct the
detailed tracking of individual credits,
with reconciliation of the reports of all
parties transferring, obtaining, or
holding credits. The Chicago Climate
Exchange provides an example of a
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Fmt 4701
Sfmt 4702
privately established trading program.
The Chicago Climate Exchange provides
a trading platform with a registry for
credits and clearing facility. The NASD
provides market surveillance and
verification of emission credits. EPA
seeks comment on how such an
independent organization could be
established; what requirements should
EPA establish for the organization; what
reporting would be required by
companies to the organization; and what
reporting would be required by the
organization to EPA.
We request comment on the
appropriateness of such an alternative
ABT program for the proposed benzene
control program and how it might work
and be enforced.
B. Vehicles
For vehicles, we considered normal
temperature standards more stringent
than Tier 2 standards, which would
likely entail hardware changes to Tier 2
vehicles. This option is discussed in
section VI. We did not consider a less
stringent standard for cold temperature
NMHC control because CAA sections
202(a) and 202(l) require us to establish
the most stringent standards achievable
considering cost and other factors. We
believe that the proposed cold NMHC
standards and phase-in for Tier 2
vehicles satisfy these CAA
requirements, and a less stringent
standard would not.
C. Gas Cans
For gas cans, as discussed in section
VIII, we are proposing an emissions
performance standard we believe
reflects the performance of the best
available control technologies. We
considered but are not proposing
options for design-based requirements,
including requirements for automatic
shut-off spouts. We also considered but
are not proposing retrofit requirements
for gas cans. These options are
discussed in sections VIII.B.3–VIII.B.5.
XI. Public Participation
We request comment on all aspects of
this proposal. This section describes
how you can participate in this process.
A. How Do I Submit Comments?
We are opening a formal comment
period by publishing this document. We
will accept comments during the period
indicated under DATES above. If you
have an interest in the proposed
emission control program described in
this document, we encourage you to
comment on any aspect of this
rulemaking. We also request comment
on specific topics identified throughout
this proposal.
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Your comments will be most useful if
you include appropriate and detailed
supporting rationale, data, and analysis.
Commenters are especially encouraged
to provide specific suggestions for any
changes to any aspect of the regulations
that they believe need to be modified or
improved. You should send all
comments, except those containing
proprietary information, to our Air
Docket (see ADDRESSES) before the end
of the comment period.
You may submit comments
electronically, by mail, or through hand
delivery/courier. To ensure proper
receipt by EPA, identify the appropriate
docket identification number in the
subject line on the first page of your
comment. Please ensure that your
comments are submitted within the
specified comment period. Comments
received after the close of the comment
period will be marked ‘‘late.’’ EPA is not
required to consider these late
comments. If you wish to submit CBI or
information that is otherwise protected
by statute, please follow the instructions
in section XI.B.
B. How Should I Submit CBI to the
Agency?
Do not submit information that you
consider to be CBI electronically
through the electronic public docket,
www.regulations.gov, or by e-mail. Send
or deliver information identified as CBI
only to the following address: U.S.
Environmental Protection Agency,
Assessment and Standards Division,
2000 Traverwood Drive, Ann Arbor, MI
48105, Attention Docket ID EPA–HQ–
OAR–2005–0036. You may claim
information that you submit to EPA as
CBI by marking any part or all of that
information as CBI (if you submit CBI
on disk or CD ROM, mark the outside
of the disk or CD ROM as CBI and then
identify electronically within the disk or
CD ROM the specific information that is
CBI). Information so marked will not be
disclosed except in accordance with
procedures set forth in 40 CFR part 2.
In addition to one complete version of
the comment that includes any
information claimed as CBI, a copy of
the comment that does not contain the
information claimed as CBI must be
submitted for inclusion in the public
docket. If you submit the copy that does
not contain CBI on disk or CD ROM,
mark the outside of the disk or CD ROM
clearly that it does not contain CBI.
Information not marked as CBI will be
included in the public docket without
prior notice. If you have any questions
about CBI or the procedures for claiming
CBI, please consult the person identified
in the FOR FURTHER INFORMATION
CONTACT section.
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C. Will There Be a Public Hearing?
We will hold a public hearing on
April 12, 2006 at the Sheraton Crystal
City Hotel, 1800 Jefferson Davis
Highway, Arlington, Virginia 22202,
Telephone: (703) 486–1111. The hearing
will start at 10 a.m. local time and
continue until everyone has had a
chance to speak.
If you would like to present testimony
at the public hearing, we ask that you
notify the contact person listed under
FOR FURTHER INFORMATION CONTACT at
least ten days before the hearing. You
should estimate the time you will need
for your presentation and identify any
needed audio/visual equipment. We
suggest that you bring copies of your
statement or other material for the EPA
panel and the audience. It would also be
helpful if you send us a copy of your
statement or other materials before the
hearing.
We will make a tentative schedule for
the order of testimony based on the
notifications we receive. This schedule
will be available on the morning of the
hearing. In addition, we will reserve a
block of time for anyone else in the
audience who wants to give testimony.
We will conduct the hearing
informally, and technical rules of
evidence won’t apply. We will arrange
for a written transcript of the hearing
and keep the official record of the
hearing open for 30 days to allow you
to submit supplementary information.
You may make arrangements for copies
of the transcript directly with the court
reporter.
D. Comment Period
The comment period for this rule will
end on May 30, 2006.
E. What Should I Consider as I Prepare
My Comments for EPA?
You may find the following
suggestions helpful for preparing your
comments:
• Explain your views as clearly as
possible.
• Describe any assumptions that you
used.
• Provide any technical information
and/or data you used that support your
views.
• If you estimate potential burden or
costs, explain how you arrived at your
estimate.
• Provide specific examples to
illustrate your concerns.
• Offer alternatives.
• Make sure to submit your
comments by the comment period
deadline identified.
• To ensure proper receipt by EPA,
identify the appropriate docket
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15921
identification number in the subject line
on the first page of your response. It
would also be helpful if you provided
the name, date, and Federal Register
citation related to your comments.
XII. Statutory and Executive Order
Reviews
A. Executive Order 12866: Regulatory
Planning and Review
Under Executive Order 12866 (58 FR
51735, October 4, 1993), the Agency
must determine whether the regulatory
action is ‘‘significant’’ and therefore
subject to Office of Management and
Budget (OMB) review and the
requirements of the Executive Order.
The Executive Order defines a
‘‘significant regulatory action’’ as one
that is likely to result in a rule that may:
• Have an annual effect on the
economy of $100 million or more or
adversely affect in a material way the
economy, a sector of the economy,
productivity, competition, jobs, the
environment, public health or safety, or
State, Local, or Tribal governments or
communities;
• Create a serious inconsistency or
otherwise interfere with an action taken
or planned by another agency;
• Materially alter the budgetary
impact of entitlements, grants, user fees,
or loan programs, or the rights and
obligations of recipients thereof; or
• Raise novel legal or policy issues
arising out of legal mandates, the
President’s priorities, or the principles
set forth in the Executive Order.
Pursuant to the terms of Executive
Order 12866, it has been determined
that this rule is a ‘‘significant regulatory
action’’ because estimated annual costs
of this rulemaking are estimated to be
over $100 million per year and it raises
novel legal or policy issues. A draft
Regulatory Impact Analysis has been
prepared and is available in the docket
for this rulemaking and at the docket
internet address listed under ADDRESSES
above. This action was submitted to the
Office of Management and Budget for
review under Executive Order 12866.
Written comments from OMB and
responses from EPA to OMB comments
are in the public docket for this
rulemaking.
B. Paperwork Reduction Act
The information collection
requirements in this proposed rule have
been submitted for approval to the
Office of Management and Budget
(OMB) under the Paperwork Reduction
Act, 44 U.S.C. 3501 et seq. The Agency
proposes to collect information to
ensure compliance with the provisions
in this rule. This includes a variety of
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requirements, both for vehicle
manufacturers, fuel producers, and
portable gasoline container
manufacturers. Information-collection
requirements related to vehicle
manufacturers are in EPA ICR #0783.50
(OMB Control Number 2060–0104);
requirements related to fuel producers
are in EPA ICR #1591.20 (OMB Control
Number 2060–0277); requirements
related to portable gasoline container
manufacturers are in EPA ICR #2213.01.
For vehicle and fuel standards, section
208(a) of the Clean Air Act requires that
manufacturers provide information the
Administrator may reasonably require to
determine compliance with the
regulations; submission of the
information is therefore mandatory. We
will consider confidential all
information meeting the requirements of
section 208(c) of the Clean Air Act. For
portable gasoline container standards,
recordkeeping and reporting
requirements for manufacturers would
be pursuant to the authority of sections
183(e) and 111 of the Clean Air Act.
As shown in Table XII.B–1, the total
annual burden associated with this
proposal is about 24,696 hours and
$2,771,309, based on a projection of 225
respondents. The estimated burden for
vehicle manufacturers and fuel
producers is a total estimate for both
new and existing reporting
requirements. The portable gasoline
container requirements represent our
first regulation of gas cans, so those
burden estimates reflect only new
reporting requirements. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, or disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; develop, acquire,
install, and utilize technology and
systems for the purposes of collecting,
validating, and verifying information,
processing and maintaining
information, and disclosing and
providing information; adjust the
existing ways to comply with any
previously applicable instructions and
requirements; train personnel to be able
to respond to a collection of
information; search data sources;
complete and review the collection of
information; and transmit or otherwise
disclose the information.
TABLE XII.B–1.—ESTIMATED BURDEN FOR REPORTING AND RECORDKEEPING REQUIREMENTS
Number of
respondents
Industry sector
Annual burden
hours
Annual costs
Vehicles .......................................................................................................................................
Fuels ............................................................................................................................................
Gas Cans .....................................................................................................................................
35
185
5
770
23,710
216
$80,900
2,677,410
12,999
Total ......................................................................................................................................
225
24,696
2,771,309
An agency may not conduct or
sponsor, and a person is not required to
respond to a collection of information
unless it displays a currently valid OMB
control number. The OMB control
numbers for EPA’s regulations are listed
in 40 CFR part 9 and 48 CFR chapter 15.
To comment on the Agency’s need for
this information, the accuracy of the
provided burden estimates, and any
suggested methods for minimizing
respondent burden, including the use of
automated collection techniques, EPA
has established a public docket for this
rule, which includes this ICR, under
Docket ID number EPA–HQ–OAR–
2005–0036. Submit any comments
related to the ICR for this proposed rule
to EPA and OMB. See ADDRESSES
section at the beginning of this notice
for where to submit comments to EPA.
Send comments to OMB at the Office of
Information and Regulatory Affairs,
Office of Management and Budget, 725
17th Street, NW., Washington, DC
20503, ‘‘Attention: Desk Office for
EPA.’’ Include the ICR number in any
correspondence. Since OMB is required
to make a decision concerning the ICR
between 30 and 60 days after March 29,
2006, a comment to OMB is best assured
of having its full effect if OMB receives
it by April 28, 2006. The final rule will
respond to any OMB or public
comments on the information collection
requirements contained in this proposal.
C. Regulatory Flexibility Act (RFA), as
Amended by the Small Business
Regulatory Enforcement Fairness Act of
1996 (SBREFA), 5 U.S.C. 601 et seq.
1. Overview
The Regulatory Flexibility Act (RFA)
generally requires an agency to prepare
a regulatory flexibility analysis of any
rule subject to notice and comment
rulemaking requirements under the
Administrative Procedure Act or any
other statute unless the agency certifies
that the rule will not have a significant
economic impact on a substantial
number of small entities. Small entities
include small businesses, small
organizations, and small governmental
jurisdictions.
For purposes of assessing the impacts
of today’s rule on small entities, small
entity is defined as: (1) A small business
as defined by the Small Business
Administration’s (SBA) regulations at 13
CFR 121.201 (see table below); (2) a
small governmental jurisdiction that is a
government of a city, county, town,
school district or special district with a
population of less than 50,000; and (3)
a small organization that is any not-forprofit enterprise which is independently
owned and operated and is not
dominant in its field. The following
table provides an overview of the
primary SBA small business categories
potentially affected by this regulation:
NAICS codes a
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Industry
Defined as small entity by SBA if less than or equal to
Light-duty vehicles:
—Vehicle manufacturers (including small volume manufacturers).
—Independent commercial importers ..................................
1,000 employees ........................................................................
336111
$6 million annual sales ..............................................................
811111,
811112,
811198
424720
335312
811198
324110
—Alternative fuel vehicle converters ...................................
Gasoline fuel refiners ..................................................................
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100 employees ...........................................................................
1,000 employees ........................................................................
$6 million annual sales ..............................................................
1500 employees b ......................................................................
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Industry
Defined as small entity by SBA if less than or equal to
Portable fuel container manufacturers:
—Plastic container manufacturers .......................................
—Metal gas can manufacturers ..........................................
NAICS codes a
500 employees ...........................................................................
1,000 employees ........................................................................
326199
332431
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Notes:
a North American Industrial Classification System.
b EPA has included in past fuels rulemakings a provision that, in order to qualify for EPA’s small refiner flexibilities, a refiner must also produce
no greater than 155,000 bpcd crude capacity.
2. Background
Mobile sources emit air toxics that
can cause cancer and other serious
health effects (Section III of this
preamble and Chapter 1 of the
Regulatory Impact Analysis (RIA) for
this rule describe these compounds and
their health effects). Mobile sources
contribute significantly to the
nationwide risk from breathing outdoor
sources of air toxics. In today’s action
we are proposing: standards to limit the
exhaust hydrocarbons from passenger
vehicles during cold temperature
operation; evaporative hydrocarbon
emissions standards for passenger
vehicles; limiting the average annual
benzene content of gasoline; and
hydrocarbon emissions standards for gas
cans that would reduce evaporation,
permeation, and spillage from these
containers. (Detailed discussion of each
of these programs is in sections VI, VII,
and VIII of the preamble and Chapters
5, 6, and 7 of the RIA). We are proposing
the standards for vehicles and gasoline
under section 202(l)(2) of the Clean Air
Act (CAA), which directs EPA to
establish requirements to control
emissions of mobile source air toxics
(MSATs) from new motor vehicles and
fuels. Controls for gas cans are being
pursued under CAA section 183(e), the
provisions applying to consumer and
commercial products.
Pursuant to section 603 of the RFA,
EPA prepared an initial regulatory
flexibility analysis (IRFA) that examines
the impact of the proposed rule on small
entities along with regulatory
alternatives that could reduce that
impact. The IRFA, as summarized
below, is available for review in the
docket and Chapter 14 of the RIA.
As required by section 609(b) of the
RFA, as amended by SBREFA, EPA also
conducted outreach to small entities
and convened a Small Business
Advocacy Review Panel to obtain advice
and recommendations of representatives
of the small entities that potentially
would be subject to the rule’s
requirements.
Consistent with the RFA/SBREFA
requirements, the Panel evaluated the
assembled materials and small-entity
comments on issues related to elements
of the IRFA. A copy of the Panel report
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is included in the docket for this
proposed rule, and a summary of the
Panel process, and subsequent Panel
recommendations, is summarized
below.
status under an MSAT program could be
much different than these initial
estimates. Current data further indicates
that these refiners produce about 2.5
percent of the total gasoline pool.
3. Summary of Regulated Small Entities
c. Portable Gasoline Container
Manufacturers
The following section discusses the
small entities directly regulated by this
proposed rule.
a. Highway Light-Duty Vehicles
In addition to the major vehicle
manufacturers, three distinct categories
of businesses relating to highway lightduty vehicles would be covered by the
new vehicle standards: small volume
manufacturers (SVMs), independent
commercial importers (ICIs), and
alternative fuel vehicle converters.
SVMs are companies that sell less than
15,000 vehicles per year, as defined in
past EPA regulations, and this status
allows vehicle models to be certified
under a slightly simpler certification
process. Independent commercial
importers are companies that hold a
Certificate (or certificates) of Conformity
permitting them to alter imported
vehicles to meet U.S emission
standards. Alternative fuel vehicle
converters are businesses that convert
gasoline or diesel vehicles to operate on
alternative fuel, and converters must
seek a certificate for all of their vehicle
models. Based on a preliminary
assessment, EPA identified about 14
SVMs, 10 alternative fuel vehicle
converters, and 10 ICIs. Of these, EPA
believes 5 SVMs, 6 converters, and all
10 ICIs would meet the small-entity
criteria as defined by SBA (no major
vehicle manufacturers meet the smallentity criteria). EPA estimates that these
small entities comprise about 0.02
percent of the total light-duty vehicle
sales in the U.S. for the year 2004.
b. Gasoline Refiners
EPA’s current assessment is that 15
refiners meet SBA’s criterion of having
1,500 employees or less. It should be
noted that because of the dynamics in
the refining industry (i.e., mergers and
acquisitions) and decisions by some
refiners to enter or leave the gasoline
market, the actual number of refiners
that ultimately qualify for small refiner
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EPA conducted a preliminary
industry profile to identify the
manufacturers of portable gasoline
containers (gas cans)—98 percent are
plastic containers and 2 percent are
metal gas cans. Using this industry
profile, EPA identified 4 domestic
manufacturers and 1 foreign
manufacturer. Of these 4 U.S.
manufacturers, 3 meet the SBA
definition of a small entity. One small
business accounted for over 50 percent
of the U.S. sales in 2002, and the other
small entities comprised about 10
percent of U.S. sales.
4. Potential Reporting, Record Keeping,
and Compliance
For highway light-duty vehicles, EPA
is proposing to continue the reporting,
recordkeeping, and compliance
requirements prescribed for this
category in 40 CFR 86. Key among these
requirements are certification
requirements and provisions related to
reporting of production, emissions
information, flexibility use, etc.
For any fuel control program, EPA
must have assurance that fuel produced
by refiners meets the applicable
standard, and that the fuel continues to
meet the standard as it passes
downstream through the distribution
system to the ultimate end user. EPA
expects that recordkeeping, reporting
and compliance provisions of the
proposed rule will be fairly consistent
with those in place today for other fuel
programs. For example, reporting would
likely involve requiring that refiners
submit pre-compliance reports updating
EPA on their plans to meet the MSAT
standards.
For gas cans, there currently are not
federal emission control requirements,
and thus, EPA is proposing new
reporting and record keeping
requirements for gas can manufacturers
that would be subject to the proposed
standards. EPA is proposing
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requirements that would be similar to
those in the California program, such as
submitting emissions testing
information, reporting of certification
families, and use of transition
provisions.
5. Relevant Federal Rules
We are aware of a few other current
or proposed Federal rules that are
related to the upcoming proposed rule.
The primary federal rules that are
related to the proposed MSAT rule
under consideration are the first MSAT
rule (Federal Register Vol. 66, p. 17230,
March 29, 2001), the Tier 2 Vehicle/
Gasoline Sulfur rulemaking (Federal
Register Vol. 65, p. 6698, February 10,
2000), the fuel sulfur rules for highway
diesel (Federal Register Vol. 66, p.
5002, January 18, 2001) and nonroad
diesel (Federal Register Vol. 69, p.
38958, June 29, 2004), and the Cold
Temperature Carbon Monoxide
Rulemaking (Federal Register Vol. 57,
p. 31888, July 17, 1992).
In addition, the Evaporative
Emissions Streamlining Direct Final
Rulemaking was issued on December 8,
2005 (Federal Register Vol. 70, p.
72917). For gas cans, OSHA has safety
regulations for gasoline containers used
in workplace settings. Cans meeting
OSHA requirements, commonly called
safety cans, are exempt from the
California program, and we are planning
to exempt them from the EPA program.
Section 1501 of the Energy Policy Act
of 2005 requires the Agency to
implement a Renewable Fuels Standard
(RFS) program. Beginning in 2006, this
program will require increasing volumes
of renewable fuel to be used in gasoline,
until a total of 7.5 billion gallons is
required in 2012. The most prevalent
renewable fuel is expected to be
ethanol. There are a wide variety of
potential impacts of ethanol blending on
MSAT emissions that will be evaluated
as part of the RFS rulemaking process.
In general, as ethanol use increases,
other sources of octane in gasoline can
decrease. Depending on these changes,
the impact on benzene emissions will
vary. The specific effects of ethanol on
benzene will be addressed in the
Regulatory Impact Analysis (RIA) to this
rule and in future rulemakings, such as
the RFS rule.
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6. Summary of SBREFA Panel Process
and Panel Outreach
a. Significant Panel Findings
The Small Business Advocacy Review
Panel (SBAR Panel, or the Panel)
considered many regulatory options and
flexibilities that would help mitigate
potential adverse effects on small
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businesses as a result of this rule.
During the SBREFA Panel process, the
Panel sought out and received
comments on the regulatory options and
flexibilities that were presented to SERs
and Panel members. The major
flexibilities and hardship relief
provisions that were recommended by
the Panel are described below and are
also located in Section 9 of the SBREFA
Final Panel Report which is available in
the public docket.
b. Panel Process
As required by section 609(b) of the
RFA, as amended by SBREFA, we also
conducted outreach to small entities
and convened an SBAR Panel to obtain
advice and recommendations of
representatives of the small entities that
potentially would be subject to the
rule’s requirements.
On September 7, 2005, EPA’s Small
Business Advocacy Chairperson
convened a Panel under Section 609(b)
of the RFA. In addition to the Chair, the
Panel consisted of the Division Director
of the Assessment and Standards
Division of EPA’s Office of
Transportation and Air Quality, the
Chief Counsel for Advocacy of the Small
Business Administration, and the
Administrator of the Office of
Information and Regulatory Affairs
within the Office of Management and
Budget. As part of the SBAR Panel
process, we conducted outreach with
representatives from the various small
entities that would be affected by the
proposed rulemaking. We met with
these Small Entity Representatives
(SERs) to discuss the potential
rulemaking approaches and potential
options to decrease the impact of the
rulemaking on their industries. We
distributed outreach materials to the
SERs; these materials included
background on the rulemaking, possible
regulatory approaches, and possible
rulemaking alternatives. The Panel met
with SERs from the industries that will
be directly affected by the MSAT rule
on September 27, 2005 (gasoline
refiners) and September 29, 2005 (lightduty vehicles and portable gasoline
containers) to discuss the outreach
materials and receive feedback on the
approaches and alternatives detailed in
the outreach packet (the Panel also met
with SERs on July 19, 2005 for an initial
outreach meeting). The Panel received
written comments from the SERs
following the meeting in response to
discussions had at the meeting and the
questions posed to the SERs by the
Agency. The SERs were specifically
asked to provide comment on regulatory
alternatives that could help to minimize
the rule’s impact on small businesses.
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In general, SERs representing the gas
can manufacturers industry raised
concerns on how the MSAT rule’s
requirements would be coordinated
with the California program and other
requirements, and that there should be
adequate opportunity for sell through at
the start of the program. The small
volume manufacturer, ICI, and vehicle
converter SERs that participated had
questions about the form of the new
standards for light-duty vehicles,
specifically testing and certification
requirements. The gasoline refiner SERs
generally stated that they believed that
small refiners would face challenges in
meeting a new standard. More
specifically, they raised the concern that
the rule could be very costly and
dependence on credits may not be a
comfortable situation; they were also
concerned about the timing of the
standards for this rule, given other
upcoming fuel standards.
The Panel’s findings and discussions
were based on the information that was
available during the term of the Panel
and issues that were raised by the SERs
during the outreach meetings and in
their comments. It was agreed that EPA
should consider the issues raised by the
SERs (and discussions had by the Panel
itself) and that EPA should consider
comments on flexibility alternatives that
would help to mitigate any negative
impacts on small businesses.
Alternatives discussed throughout the
Panel process included those offered in
previous or current EPA rulemakings, as
well as alternatives suggested by SERs
and Panel members, and the Panel
recommended that all be considered in
the development of the rule. Though
some of the flexibilities suggested may
be appropriate to apply to all entities
affected by the rulemaking, the Panel’s
discussions and recommendations were
focused mainly on the impacts, and
ways to mitigate adverse impacts, on
small businesses. A summary of these
recommendations is detailed below, and
a full discussion of the regulatory
alternatives and hardship provisions
discussed and recommended by the
Panel can be found in the SBREFA Final
Panel Report. A complete discussion of
the transition and hardship provisions
that we are proposing in today’s action
can be found in Sections VI.E, VII.E, and
VIII (vehicle, fuels, and gas can sections)
of this preamble. Also, the Panel Report
includes all comments received from
SERs (Appendices D and E of the
Report) and summaries of the two
outreach meetings that were held with
the SERs (Appendices B and C). In
accordance with the RFA/SBREFA
requirements, the Panel evaluated the
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aforementioned materials and SER
comments on issues related to the Initial
Regulatory Flexibility Analysis (IRFA).
The following sections describe the
Panel recommendations from the SBAR
Panel Report.
c. Small Business Flexibilities
The Panel recommended that EPA
consider and seek comment on a wide
range of regulatory alternatives to
mitigate the impacts of the rulemaking
on small businesses, including those
flexibility options described below. As
previously stated, the following
discussion is a summary of the SBAR
Panel recommendations; our proposals
regarding these recommendations are
located in earlier sections of this rule
preamble.
i. Highway Light-Duty Vehicles
wwhite on PROD1PC61 with PROPOSALS2
(a) Highway Light-Duty Vehicle
Flexibilities
For certification purposes (and for the
sake of simplicity for Panel discussions
regarding flexibility options), SVMs
include ICIs and alternative fuel vehicle
converters since they sell less than
15,000 vehicles per year. Similar to the
flexibility provisions implemented in
the Tier 2 rule, the Panel recommended
that we allow SVMs (includes all
vehicle small entities that would be
affected by this rule, which are the
majority of SVMs) the following
flexibility options for meeting cold
temperature VOC standards and
evaporative emission standards:
For cold VOC standards, the Panel
recommended that SVMs simply
comply with the standards with 100
percent of their vehicles during the last
year of the 4 year phase-in period. For
example, if the standard for light-duty
vehicles and light light-duty trucks (0 to
6,000 pounds GVWR) were to begin in
2010 and end in 2013 (25%, 50%, 75%,
100% phase-in over 4 years), the SVM
provision would be 100 percent in 2013.
If the standard for heavy light-duty
trucks and medium-duty passenger
vehicles (greater than 6,000 pounds
GVWR) were to start in 2012 (25%,
50%, 75%, 100% phase-in over 4 years),
the SVM provision would be 100
percent in 2015.
In regard to evaporative emission
standards, the Panel recommended that
since the evaporative emissions
standards will not have phase-in years,
we allow SVMs to simply comply with
standards during the third year of the
program (we have implemented similar
provisions in past rulemakings). For a
2009 start date for light-duty vehicles
and light light-duty trucks, SVMs would
need to meet the evaporative emission
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standards in 2011. For a 2010
implementation date for heavy lightduty trucks and medium-duty passenger
vehicles, SVMs would need to comply
in 2012.
(b) Highway Light-Duty Vehicle
Hardships
In addition, the Panel recommended
that hardship flexibility provisions be
extended to SVMs for the cold
temperature VOC and evaporative
emission standards. The provisions that
the Panel recommended are:
SVMs would be allowed to apply
(EPA would need to review and approve
application) for up to an additional 2
years to meet the 100 percent phase-in
requirements for cold VOC and the
delayed requirement for evaporative
emissions. Appeals for such hardship
relief must be made in writing, must be
submitted before the earliest date of
noncompliance, must include evidence
that the noncompliance will occur
despite the manufacturer’s best efforts to
comply, and must include evidence that
severe economic hardship will be faced
by the company if the relief is not
granted.
ii. Gasoline Refiners
(a) Gasoline Refiner Flexibilities
The Panel recommended that EPA
propose certain provisions to encourage
early compliance with lower benzene
standards. The Panel recommended that
EPA propose that small refiners be
afforded the following flexibility
options to help mitigate the impacts on
small refiners:
Delay in Standards—The Panel
recommended that a four-year delay
period be proposed for small refiners. A
four-year delay would be needed in
order to allow for a review of the ABT
program, as discussed below, to occur
one year after implementation but still
three years prior to the small refiner
compliance deadline. It was noted by
the small refiners that three years are
generally needed for small refiners to
obtain financing and perform
engineering and construction. The Panel
was also in support of allowing for
refinery expansion within the delay
option, and recommended that refinery
expansion be provided for in the rule.
Early ABT Credits—The Panel
recommended that early credit
generation be afforded to small refiners
that take some steps to meet the benzene
requirement prior to the effective date of
the standard. Depending on the start
date of the program, and coupled with
the four-year delay option, a small
refiner could have a total credit
generation period of five to seven years.
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The Panel was also in support of
allowing refiners (small, as well as nonsmall, refiners) to generate credits for
reductions to their benzene emissions
levels, rather than credits only for
meeting the benzene standard that is set
by the rule.
The Panel recommended a review of
the credit trading program and small
refiner flexibility options one year after
the general program starts. Such a
review could take into account the
number of early credits generated, as
well as the number of credits generated
and sold during the first year of the
program. Further, a review after the first
year of the program would still provide
small refiners with the three years that
it was suggested would be needed for
these refiners to obtain financing and
perform engineering and construction
for benzene reduction equipment.
Should the review conclude that
changes to either the program or the
small refiner provisions are necessary,
the Panel recommended that EPA also
consider some of the suggestions
provided by the small refiners (their
comments are located in Appendix E of
the Final Panel Report), such as:
• The general MSAT program should
require pre-compliance reporting
(similar to EPA’s highway and nonroad
diesel rules);
• Following the review, EPA should
revisit the small refiner provisions if it
is found that the credit trading market
does not exist, or if credits are only
available at a cost that would not allow
small refiners to purchase credits for
compliance;
• The review should offer ways either
to help the credit market, or help small
refiners gain access to credits (e.g., EPA
could ‘‘create’’ credits to introduce to
the market, EPA could impose
additional requirements to encourage
trading with small refiners, etc.).
In addition, the Panel recommended
that EPA consider in this rulemaking
establishing an additional hardship
provision to assist those small refiners
that cannot comply with the MSAT with
a viable credit market. (This suggested
hardship provision was also suggested
by the small refiners in their comments,
located in Appendix E of the Final
Panel Report). This hardship provision
could address concerns that, for some
small refineries, compliance may be
technically feasible only through the
purchase of credits and it may not be
economically feasible to purchase those
credits. This flexibility could be
provided to a small refiner on a case-bycase basis following the review and
based on a summary, by the refiner, of
technical or financial infeasibility (or
some other type of similar situation that
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would render its compliance with the
standard difficult). This hardship
provision might include further delays
and/or a slightly relaxed standard on an
individual refinery basis for a duration
of two years; in addition, provision
might allow the refinery to request, and
EPA grant, multiple extensions of the
flexibility until the refinery’s material
situation changes. The Panel also stated
that it understood that EPA may need to
modify or rescind this provision, should
it be implemented, based on the results
of the program review.
(b) Gasoline Refiner Hardships
During the Panel process, we stated
that we intended to propose the extreme
unforeseen circumstances hardship and
extreme hardship provisions (for all
gasoline refiners and importers), similar
to those in prior fuels programs. A
hardship based on extreme unforeseen
circumstances is intended to provide
short term relief due to unanticipated
circumstances beyond the control of the
refiner, such as a natural disaster or a
refinery fire; an extreme hardship is
intended to provide short-term relief
based on extreme circumstances (e.g.,
extreme financial problems, extreme
operational or technical problems, etc.)
that impose extreme hardship and thus
significantly affect a refiner’s ability to
comply with the program requirements
by the applicable dates. The Panel
agreed with the proposal of such
provisions and recommended that we
include them in the MSAT rulemaking.
iii. Portable Gasoline Containers
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(a) Portable Gasoline Container
Flexibilities
Since nearly all gas can manufacturers
are small entities and they account for
about 60 percent of sales, the Panel
planned to extend the flexibility options
to all gas can manufacturers. Moreover,
implementation of the program would
be much simpler by doing so. The
recommended flexibilities are the
following:
Design Certification—The Panel
recommended that we propose to permit
gas can manufacturers to use design
certification in lieu of running any or all
of the durability aging cycles.
Manufacturers could demonstrate the
durability of their gas cans based in part
on emissions test data from designs
using the same permeation barriers and
materials. Under a design-based
certification program a manufacturer
would provide evidence in the
application for certification that their
container would meet the applicable
standards based on its design (e.g., use
of a particular permeation barrier). The
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manufacturer would submit adequate
engineering and other information about
its individual design such that EPA
could determine that the emissions
performance of their individual design
would not be negatively impacted by
slosh, UV exposure, and/or pressure
cycling (whichever tests the
manufacturer is proposing to not run
prior to emissions testing).
Broaden Certification Families—This
approach would relax the criteria used
to determine what constitutes a
certification family. It would allow
small businesses to limit their
certification families (and therefore their
certification testing burden), rather than
testing all of the various size containers
in a manufacturer’s product line. Some
small entities may be able to put all of
their various size containers into a
single certification family.
Manufacturers would then certify their
containers using the ‘‘worst case’’
configuration within the family. To be
grouped together, containers would
need to be manufactured using the same
materials and processes even though
they are of different sizes.
Additional Lead-time—Since it may
take additional time for the gas can
SERs to gather information to fully
evaluate whether or not additional leadtime is needed beyond the 2009 start
date, the Panel recommended that we
discuss lead-time in the proposal and
request comments on the need for
additional lead-time to allow
manufacturers to ramp up to a
nationwide program.
Product Sell-through—As with past
rulemakings for other source sectors, the
Panel recommended that EPA propose
to allow normal sell through of gas cans
as long as manufacturers do not create
stockpiles of noncomplying gas cans
prior to the start of the program.
(b) Portable Gasoline Container
Hardships
The Panel recommended that EPA
propose two types of hardship programs
for small gas can manufacturers. These
provisions are:
Allow small manufacturers to petition
EPA for limited additional lead-time to
comply with the standards. A
manufacturer would have to make the
case that it has taken all possible
business, technical, and economic steps
to comply but the burden of compliance
costs would have a significant adverse
effect on the company’s solvency.
Hardship relief could include
requirements for interim emission
reductions. The length of the hardship
relief would be established during the
initial review and would likely need to
be reviewed annually thereafter.
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Permit small manufacturers to apply
for hardship relief if circumstances
outside their control cause the failure to
comply (i.e. supply contract broken by
parts supplier) and if failure to sell the
subject containers would have a major
impact on the company’s solvency. The
terms and timeframe of the relief would
depend on the specific circumstances of
the company and the situation involved.
As part of its application, a company
would be required to provide a
compliance plan detailing when and
how it would achieve compliance with
the standards under both types of
hardship relief.
We invite comments on all aspects of
the proposal and its impacts on small
entities.
D. Unfunded Mandates Reform Act
Title II of the Unfunded Mandates
Reform Act of 1995 (UMRA), Public
Law 104–4, establishes requirements for
Federal agencies to assess the effects of
their regulatory actions on State, local,
and tribal governments and the private
sector. Under section 202 of the UMRA,
EPA generally must prepare a written
statement, including a cost-benefit
analysis, for proposed and final rules
with ‘‘Federal mandates’’ that may
result in expenditures to State, local,
and tribal governments, in the aggregate,
or to the private sector, of $100 million
or more in any one year. Before
promulgating an EPA rule for which a
written statement is needed, section 205
of the UMRA generally requires EPA to
identify and consider a reasonable
number of regulatory alternatives and
adopt the least costly, most costeffective, or least burdensome
alternative that achieves the objectives
of the rule. The provisions of section
205 do not apply when they are
inconsistent with applicable law.
Moreover, section 205 allows EPA to
adopt an alternative other than the least
costly, most cost-effective, or least
burdensome alternative if the
Administrator publishes with the final
rule an explanation of why that
alternative was not adopted.
Before EPA establishes any regulatory
requirements that may significantly or
uniquely affect small governments,
including tribal governments, it must
have developed under section 203 of the
UMRA a small government agency plan.
The plan must provide for notifying
potentially affected small governments,
enabling officials of affected small
governments to have meaningful and
timely input in the development of EPA
regulatory proposals with significant
federal intergovernmental mandates,
and informing, educating, and advising
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small governments on compliance with
the regulatory requirements.
This rule contains no federal
mandates for state, local, or tribal
governments as defined by the
provisions of Title II of the UMRA. The
rule imposes no enforceable duties on
any of these governmental entities.
Nothing in the rule would significantly
or uniquely affect small governments.
EPA has determined that this rule
contains federal mandates that may
result in expenditures of more than
$100 million to the private sector in any
single year. EPA believes that the
proposal represents the least costly,
most cost-effective approach to achieve
the statutory requirements of the rule.
The costs and benefits associated with
the proposal are discussed above and in
the Draft Regulatory Impact Analysis, as
required by the UMRA.
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E. Executive Order 13132: Federalism
Executive Order 13132, entitled
‘‘Federalism’’ (64 FR 43255, August 10,
1999), requires EPA to develop an
accountable process to ensure
‘‘meaningful and timely input by State
and local officials in the development of
regulatory policies that have federalism
implications.’’ ‘‘Policies that have
federalism implications’’ is defined in
the Executive Order to include
regulations that have ‘‘substantial direct
effects on the States, on the relationship
between the national government and
the States, or on the distribution of
power and responsibilities among the
various levels of government.’’
This proposed rule does not have
federalism implications. It will not have
substantial direct effects on the States,
on the relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government, as specified in
Executive Order 13132.
Although section 6 of Executive Order
13132 does not apply to this rule, EPA
did consult with representatives of
various State and local governments in
developing this rule. EPA has also
consulted representatives from
STAPPA/ALAPCO, which represents
state and local air pollution officials.
In the spirit of Executive Order 13132,
and consistent with EPA policy to
promote communications between EPA
and State and local governments, EPA
specifically solicits comment on this
proposed rule from State and local
officials.
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F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
Executive Order 13175, entitled
‘‘Consultation and Coordination with
Indian Tribal Governments’’ (65 FR
67249, November 9, 2000), requires EPA
to develop an accountable process to
ensure ‘‘meaningful and timely input by
tribal officials in the development of
regulatory policies that have tribal
implications.’’
This proposed rule does not have
tribal implications as specified in
Executive Order 13175. This rule will be
implemented at the Federal level and
impose compliance costs only on
vehicle manufacturers (includes
alternative fuel vehicle converters and
ICIs), fuel producers, and portable
gasoline container manufacturers. Tribal
governments will be affected only to the
extent they purchase and use regulated
vehicles, fuels, and portable gasoline
containers. Thus, Executive Order
13175 does not apply to this rule. EPA
specifically solicits additional comment
on this proposed rule from tribal
officials.
G. Executive Order 13045: Protection of
Children From Environmental Health
and Safety Risks
Executive Order 13045, ‘‘Protection of
Children from Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997) applies to any rule that
(1) is determined to be ‘‘economically
significant’’ as defined under Executive
Order 12866, and (2) concerns an
environmental health or safety risk that
EPA has reason to believe may have a
disproportionate effect on children. If
the regulatory action meets both criteria,
section 5–501 of the Order directs the
Agency to evaluate the environmental
health or safety effects of the planned
rule on children, and explain why the
planned regulation is preferable to other
potentially effective and reasonably
feasible alternatives considered by the
Agency.
This proposed rule is subject to the
Executive Order because it is an
economically significant regulatory
action as defined by Executive Order
12866, and we believe that by
addressing the environmental health or
safety risk, this action may have a
disproportionate beneficial effect on
children. Accordingly, we have
evaluated the potential environmental
health or safety effects of VOC and
toxics emissions from gasoline-fueled
mobile sources and gas cans on
children. The results of this evaluation
are described below and contained in
section IV.
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Exposure to a number of the
compounds addressed in this rule may
have a disproportionate effect on
children. First, exposure to carcinogens
that cause cancer through a mutagenic
mode of action during childhood
development may have an
incrementally disproportionate impact.
Because of their small size, increased
activity, and increased ventilation rates
compared to adults, children may have
greater exposure to these compounds in
the ambient air, on a unit body weight
basis. Moreover, for PM, because
children’s breathing rates are higher,
their exposures may be higher and
because their respiratory systems are
still developing, children may be more
susceptible to problems from exposure
to respiratory irritants. The public is
invited to submit or identify peerreviewed studies and data, of which
EPA may not be aware, that assessed
results of early life exposure to the
pollutants addressed by this rule.
H. Executive Order 13211: Actions That
Significantly Affect Energy Supply,
Distribution, or Use
This rule is not a ‘‘significant energy
action’’ as defined in Executive Order
13211, ‘‘Actions Concerning Regulations
That Significantly Affect Energy Supply,
Distribution, or Use’’ (66 FR 28355 (May
22, 2001)) because it is not likely to
have a significant adverse effect on the
supply, distribution, or use of energy. If
promulgated, the gasoline benzene
provisions of the proposed rule would
shift about 22,000 barrels per day of
benzene from the gasoline market to the
petrochemical market. This volume
represents about 0.2 percent of
nationwide gasoline production. The
actual impact of the rule on the gasoline
market, however, is likely to be less due
to offsetting changes in the production
of petrochemicals, as well as expected
growth in the petrochemical market
absent this rule. The major sources of
benzene for the petrochemical market
other than reformate from gasoline
production are also derived from
gasoline components or gasoline
feedstocks. Consequently, the expected
shift toward more benzene production
from reformate due to this proposed rule
would be offset by less benzene
produced from other gasoline
feedstocks.
The rule would require refiners to use
a small additional amount of energy in
processing gasoline to reduce benzene
levels, primarily due to the increased
energy used for benzene extraction. Our
modeling of increased energy use
indicates that the process energy used
by refiners to produce gasoline would
increase by about one percent. Overall,
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we believe that the proposed rule would
result in no significant adverse energy
impacts.
The proposed gasoline benzene
provisions would not affect the current
gasoline distribution practices.
We discuss our analysis of the energy
and supply effects of the proposed
gasoline benzene standard further in
section IX of this preamble and in
Chapter 9 of the Regulatory Impact
Analysis.
The fuel supply and energy effects
described above would be offset
substantially by the positive effects on
gasoline supply and energy use of the
proposed gas can standards also
proposed in today’s action. These
proposed provisions would greatly
reduce the gasoline lost to evaporation
from gas cans. This would in turn
reduce the demand for gasoline,
increasing the gasoline supply and
reducing the energy used in producing
gasoline.
I. National Technology Transfer
Advancement Act
Section 12(d) of the National
Technology Transfer and Advancement
Act of 1995 (‘‘NTTAA’’), Public Law No.
104–113, 12(d) (15 U.S.C. 272 note)
directs EPA to use voluntary consensus
standards in its regulatory activities
unless to do so would be inconsistent
with applicable law or otherwise
impractical. Voluntary consensus
standards are technical standards (e.g.,
materials specifications, test methods,
sampling procedures, and business
practices) that are developed or adopted
by voluntary consensus standards
bodies. The NTTAA directs EPA to
provide Congress, through OMB,
explanations when the Agency decides
not to use available and applicable
voluntary consensus standards.
The proposed rulemaking involves
technical standards. Therefore, the
Agency conducted a search to identify
potentially applicable voluntary
consensus standards. However, we
identified no such standards. Therefore,
for the cold temperature NMHC
standards, EPA proposes to use the
existing EPA cold temperature CO test
procedures (manufacturers currently
measure hydrocarbon emissions with
current cold CO test procedures), which
were adopted in a previous EPA
rulemaking (1992). The fuel standards
referenced in today’s proposed rule
involve the measurement of gasoline
fuel parameters. The measurement
standards for gasoline fuel parameters
referenced in today’s proposal are
government-unique standards that were
developed by the Agency through
previous rulemakings. Both the cold
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temperature CO test procedures and the
measurement standards for gasoline fuel
parameters have served the Agency’s
emissions control goals well since their
implementation and have been well
accepted by industry. For gas cans, EPA
is proposing new procedures for
measuring hydrocarbon emissions.
EPA welcomes comments on this
aspect of the proposed rulemaking and,
specifically, invites the public to
identify potentially-applicable
voluntary consensus standards and to
explain why such standards should be
used in this regulation.
and 301(a) of the CAA, 42 U.S.C.
sections 7414(a) and 7601(a).
Statutory authority for the vehicle
controls proposed in this document can
be found in sections 202, 206, 207, 208,
and 301 of the CAA, 42 U.S.C. sections
7521, 7525, 7541, 7542 and 7601.
Statutory authority for the portable
gasoline container controls proposed in
today’s document can be found in
sections 183(e) and 111, 42 U.S.C.
sections 7511b(e) and 7411.
J. Executive Order 12898: Federal
Actions To Address Environmental
Justice in Minority Populations and
Low-Income Populations
Environmental protection,
Administrative practice and procedure,
Confidential business information,
Incorporation by reference, Labeling,
Consumer or Commercial Products
pollution, Penalties, Reporting and
recordkeeping requirements.
Executive Order 12898 directs Federal
agencies to ‘‘determine whether their
programs, policies, and activities have
disproportionately high adverse human
health or environmental effects on
minority populations’ (sections 3–301
and 3–302). In developing this proposed
rule, EPA assessed environmental
justice issues that may be relevant to
this proposal (see section IV of this
proposed rule and chapter 3 of the Draft
Regulatory Impact Analysis).
The proposed rule would reduce VOC
and toxics emissions from gasolinefueled mobile sources (particularly
highway light-duty vehicles) and gas
cans, and thus, it would decrease the
amount of air pollution to which the
entire population is exposed. EPA
evaluated the population residing close
to high traffic density (near roadways),
and we found that this population has
demographic differences from the
general population, including a greater
fraction of lower income and minority
residents. Since the proposed rule
would reduce emissions from roadways,
those living nearby (more likely to be
lower income and minority residents)
are likely to have a disproportionate
benefit from the proposed rule. Thus,
this proposed rule does not have a
disproportionately high adverse human
health or environmental effect on
minority populations.
XIII. Statutory Provisions and Legal
Authority
Statutory authority for the fuels
controls proposed in today’s document
can be found in sections 202 and 211(c)
of the Clean Air Act (CAA), as amended,
42 U.S.C. sections 7521 and 7545(c).
Additional support for the procedural
and enforcement-related aspects of the
fuel controls in today’s proposal,
including the proposed recordkeeping
requirements, come from sections 114(a)
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List of Subjects
40 CFR Part 59
40 CFR Part 80
Environmental protection, Air
pollution control, Fuel additives,
Gasoline, Imports, Incorporation by
reference, Labeling, Motor vehicle
pollution, Penalties, Reporting and
recordkeeping requirements.
40 CFR Part 85
Environmental protection,
Administrative practice and procedure,
Confidential business information,
Imports, Labeling, Motor vehicle
pollution, Penalties, Reporting and
recordkeeping requirements, Research,
Warranties.
40 CFR Part 86
Environmental protection,
Administrative practice and procedure,
Confidential business information,
Incorporation by reference, Labeling,
Motor vehicle pollution, Penalties,
Reporting and recordkeeping
requirements.
Dated: February 28, 2006.
Stephen L. Johnson,
Administrator.
For the reasons set forth in the
preamble, parts 59, 80, 85 and 86 of title
40 of the Code of Federal Regulations
are proposed to be amended as follows:
PART 59—NATIONAL VOLATILE
ORGANIC COMPOUND EMISSION
STANDARDS FOR CONSUMER AND
COMMERCIAL PRODUCTS
1. The authority citation for part 59
continues to read as follows:
Authority: 42 U.S.C. 7414 and 7511b(e).
2. Subpart F is added to part 59 to
read as follows:
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59.697 State actions.
59.698 May EPA enter my facilities for
inspections?
59.699 How do I request a hearing?
Subpart F—Control of Evaporative
Emissions From New and In-Use
Portable Gasoline Containers
Sec.
Overview and Applicability
59.600 Does this subpart apply for my
products?
59.601 Do the requirements of this subpart
apply to me?
59.602 What are the general prohibitions
and requirements of this subpart?
59.603 How must manufacturers apply
good engineering judgment?
59.605 What portable gasoline containers
are excluded from this subpart’s
requirements?
59.607 Submission of information.
Emission Standards and Related
Requirements
59.611 What evaporative emission
requirements apply under this subpart?
59.612 What emission-related warranty
requirements apply to me?
59.613 What operation and maintenance
instructions must I give to buyers?
59.615 How must I label and identify the
portable gasoline containers I produce?
Certifying Emission Families
59.621 Who may apply for a certificate of
conformity?
59.622 What are the general requirements
for obtaining a certificate of conformity
and producing portable gasoline
containers under it?
59.623 What must I include in my
application?
59.624 How do I amend my application for
certification?
59.625 How do I select emission families?
59.626 What emission testing must I
perform for my application for a
certificate of conformity?
59.627 How do I demonstrate that my
emission family complies with
evaporative emission standards?
59.628 What records must I keep and what
reports must I send to EPA?
59.629 What decisions may EPA make
regarding my certificate of conformity?
59.630 EPA testing.
59.650 General testing provisions.
59.652 Other procedures.
59.653 How do I test portable gasoline
containers?
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Special Compliance Provisions
59.660 Exemption from the standards.
59.662 What temporary provisions address
hardship due to unusual circumstances?
59.663 What are the provisions for
extending compliance deadlines for
manufacturers under hardship?
59.664 What are the requirements for
importing portable gasoline containers
into the United States?
Definitions and Other Reference Information
59.680 What definitions apply to this
subpart?
59.685 What symbols, acronyms, and
abbreviations does this subpart use?
59.695 What provisions apply to
confidential information?
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Subpart F—Control of Evaporative
Emissions From New and In-Use
Portable Gasoline Containers
Overview and Applicability
§ 59.600 Does this subpart apply for my
products?
(a) Except as provided in § 59.605 and
paragraph (b) and (c) of this section, the
regulations in this subpart F apply for
all portable gasoline containers (defined
in § 59.680) beginning January 1, 2009.
(b) See § 59.602(a) and (b) to
determine how to apply the provisions
of this subpart for containers that were
manufactured before January 1, 2009.
§ 59.601 Do the requirements of this
subpart apply to me?
(a) Unless specified otherwise in this
subpart, the requirements and
prohibitions of this subpart apply to all
manufacturers and importers of portable
gasoline containers. Certain prohibitions
in § 59.602 apply to all other persons.
(b) New portable gasoline containers
that are subject to the emissions
standards of this part must be covered
by a certificate of conformity that is
issued to the manufacturer of the
container. If more than one person
meets the definition of manufacturer for
a portable gasoline container, see
§ 59.621 to determine if you are the
manufacturer who may apply for and
receive a certificate of conformity.
(c) Unless specifically noted
otherwise, the term ‘‘you’’ means
manufacturers, as defined in § 59.680.
§ 59.602 What are the general prohibitions
and requirements of this subpart?
(a) General prohibition for
manufacturers and importers. No
manufacturer or importer may sell, offer
for sale, introduce or deliver for
introduction into commerce in the
United States, or import any new
portable gasoline container that is
subject to the emissions standards of
this subpart and is manufactured after
December 31, 2008 unless it is covered
by a valid certificate of conformity, it is
labeled as required, and it complies
with all of the applicable requirements
of this subpart, including complies with
the emissions standards for its useful
life. After June 30, 2009, no
manufacturer or importer may sell, offer
for sale, introduce into commerce in the
United States, or import any new
portable gasoline container that was
manufactured prior to January 1, 2009.
(b) General prohibition for wholesale
distributors. No wholesale distributor
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may sell, offer for sale, or distribute any
portable gasoline container that is
subject to the emissions standards of
this subpart and is manufactured after
December 31, 2008 unless it is covered
by a valid certificate of conformity and
is labeled as required. After December
31, 2009, no wholesale distributor may
sell, offer for sale, or distribute any
portable gasoline container that was
manufactured prior to January 1, 2009.
After December 31, 2009, all new
portable gasoline containers shall be
deemed to be manufactured after
December 31, 2008 unless they are in
retail inventory.
(c) Reporting and recordkeeping. (1)
You must keep the records and submit
the reports specified in § 59.628.
Records must be retained for at least 5
years from the date of manufacture or
importation and must be supplied to
EPA upon request.
(2) No person may alter, destroy, or
falsify any record or report required by
this subpart.
(d) Testing and access to facilities.
You may not keep us from entering your
facility to test inspect if we are
authorized to do so. Also, you must
perform the tests we require (or have the
tests done for you). Failure to perform
this testing is prohibited.
(e) Warranty. You may not fail to
offer, provide notice of, or honor the
emissions warranty required under this
subpart.
(f) Replacement components. No
person may sell, offer for sale, introduce
or deliver for introduction into
commerce in the United States, import,
or install any replacement component
for portable gasoline containers subject
to the standards of this subpart where
the component has the effect of
disabling, bypassing, or rendering
inoperative the emissions controls of the
containers.
(g) Violations. If a person violates any
prohibition or requirement of this
subpart or the Act concerning portable
gasoline containers, it shall be
considered a separate violation for each
portable gasoline container.
(h) Assessment of penalties and
injunctions. We may assess
administrative penalties, bring a civil
action to assess and recover civil
penalties, bring a civil action to enjoin
and restrain violations, or bring criminal
action as provided by the Clean Air Act.
§ 59.603 How must manufacturers apply
good engineering judgment?
(a) In addition to other requirements
and prohibitions set forth in this
subpart, you must use good engineering
judgment for decisions related to any
requirements under this subpart. This
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includes your applications for
certification, any testing you do to show
that your portable gasoline containers
comply with requirements that apply to
them, and how you select, categorize,
determine, and apply these
requirements.
(b) Upon request, you must provide
EPA a written description of the
engineering judgment in question. Such
information must be provided within 15
working days unless EPA specifies a
different period of time to respond.
(c) We may reject your decision if it
is not based on good engineering
judgment or is otherwise inconsistent
with the requirements that apply, and
we may:
(1) Suspend, revoke, or void a
certificate of conformity if we determine
you used incorrect or incomplete
information or failed to consider
relevant information, or that your
decision was not based on good
engineering judgment; or
(2) Notify you that we believe any
aspect of your application or other
information submission may be
incorrect or invalid due to lack of good
engineering judgment or other cause.
Unless a different period of time is
specified, you will have 30 days to
respond to our notice and specifically
address our concerns. After considering
your information, we will notify
regarding our finding, which may
include the actions provided in
paragraph (c)(1) of this section.
(d) If you disagree with our
conclusions under paragraph (c) of this
section, you may file a request for a
hearing with the Designated Compliance
Officer as described in § 59.699. In your
request, you must specifically state your
objections, and include relevant data or
supporting analysis. The request must
be signed by your authorized
representative. If we agree that your
request raises a substantial factual issue,
we will hold the hearing according to
§ 59.699.
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§ 59.605 What portable gasoline
containers are excluded from this subpart’s
requirements?
This section describes exclusions that
apply to certain portable gasoline
containers. The prohibitions and
requirements of this subpart do not
apply for containers excluded under
this section. Exclusions under this
section are based on inherent
characteristics of the containers. See
§ 59.660 for exemptions that apply
based on special circumstances.
(a) Containers approved as safety cans
consistent with the requirements of
Title 29, part 1926, subpart F, of the
Code of Federal Regulations (29 CFR
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1926.150 through 1926.152) are
excluded. Such cans generally have a
flash-arresting screens, spring-closing
lids and spout covers and have been
approved by a nationally recognized
testing laboratory such as Factory
Mutual Engineering Corp.,
Underwriters’ Laboratories, Inc., or
Federal agencies such as Bureau of
Mines, or U.S. Coast Guard.
(b) Containers with a nominal
capacity of less than 0.25 gallons or
more than 10.0 gallons are excluded.
(c) Containers designed and marketed
solely to deliver fuel directly to nonroad
engines during engine operation, such
as containers with a connection for a
fuel line and a reserve fuel area, are
considered to be nonroad fuel tanks,
and are thus excluded.
§ 59.607
Submission of information.
(a) You are responsible for all
statements you make to us related to
this subpart F, including information
not required during certification. You
are required to provide truthful and
complete information. This subpart
describes the consequences of failing to
meet this obligation. The consequences
also may include prosecution under 18
U.S.C. 1001 and 42 U.S.C. 7431(c)(2).
(b) We may require an officer or
authorized representative of your
company with knowledge of the other
information contained in the submittal
to approve and sign any submission of
information to us, and to certify that all
of the information submitted is accurate
and complete.
Emission Standards and Related
Requirements
§ 59.611 What evaporative emission
requirements apply under this subpart?
(a) Emissions from portable gasoline
containers may not exceed 0.30 grams
per gallon per day when measured with
the test procedures in §§ 59.650 through
59.653. This procedure measures
diurnal venting emissions and
permeation emissions.
(b) For the purpose of this section,
portable gasoline containers include
spouts, caps, gaskets, and other parts
provided with the container.
(c) The following general
requirements also apply for all portable
gasoline containers subject to the
standards of this subpart:
(1) Prohibited controls. You may not
design your emission-control systems so
that they cause or contribute to an
unreasonable risk to public health,
welfare, or safety while operating. You
may not design your portable gasoline
containers to have adjustable parameters
unless the containers will meet all the
requirements of this subpart when
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adjusted anywhere within the
physically adjustable range. You may
not equip your portable gasoline
containers with a defeat device, or
intentionally produce your containers to
enable the use of a defeat device. A
defeat device is an element of design
(either original or replacement) that is
not approved in advance by EPA and
that reduces the effectiveness of
emission controls under conditions that
the portable gasoline containers may
reasonably be expected to encounter
during normal use.
(2) Leaks. You must design and
manufacture your containers to be free
of leaks. This requirement applies when
your container is upright, partially
inverted, or completely inverted.
(3) Refueling. You are required to
design your portable gasoline containers
to minimize spillage during refueling to
the extent practical. This requires that
you use good engineering judgment to
avoid designs that will make it difficult
to refuel typical vehicle and equipment
designs without spillage.
(d) Portable gasoline containers must
meet the standards and requirements
specified in this subpart throughout the
useful life of the container. The useful
life of the container is five years
beginning on the date of sale to the
ultimate purchaser.
§ 59.612 What emission-related warranty
requirements apply to me?
(a) General requirements. You must
warrant to the ultimate purchaser that
the new portable gasoline container,
including all parts of its evaporative
emission-control system, is:
(1) Designed, built, and equipped so
it conforms at the time of sale to the
ultimate purchaser with the
requirements of this subpart.
(2) Is free from defects in materials
and workmanship that may keep it from
meeting these requirements.
(b) Warranty notice and period. Your
emission-related warranty must be valid
for a minimum of one year from the date
of sale to the ultimate purchaser.
(c) Notice. You must provide a
warranty notice with each container.
§ 59.613 What operation and maintenance
instructions must I give to buyers?
You must provide the ultimate
purchaser of the new portable gasoline
container written instructions for
properly maintaining and using the
emission-control system.
§ 59.615 How must I label and identify the
portable gasoline containers I produce?
This section describes how you must
label your portable gasoline containers.
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(a) At the time of manufacture,
indelibly mark the month and year of
manufacture on each container.
(b) Mold into or affix a legible label
identifying each portable gasoline
container. The label must be:
(1) Attached so it is not easily
removable.
(2) Secured to a part of the container
that can be easily viewed when the can
is in use, not on the bottom of the
container.
(3) Written in English.
(c) The label must include:
(1) The heading ‘‘EMISSION
CONTROL INFORMATION’’.
(2) Your full corporate name and
trademark.
(3) A standardized identifier such as
EPA’s standardized designation for the
emission families, the model number, or
the part number.
(4) This statement: ‘‘THIS
CONTAINER COMPLIES WITH U.S.
EPA EMISSION REGULATIONS FOR
PORTABLE GASOLINE
CONTAINERS.’’.
(d) You may add information to the
emission control information label to
identify other emission standards that
the container meets or does not meet
(such as California standards). You may
also add other information to ensure
that the portable gasoline container will
be properly maintained and used.
(e) You may request EPA to approve
modified labeling requirements in this
subpart F if you show that it is
necessary or appropriate. We will
approve your request if your alternate
label is consistent with the requirements
of this subpart.
(f) You may identify the name and
trademark of another company instead
of their own on your emission control
information label, subject to the
following provisions:
(1) You must have a contractual
agreement with the other company that
obligates that company to take the
following steps:
(i) Meet the emission warranty
requirements that apply under § 59.612.
This may involve a separate agreement
involving reimbursement of warrantyrelated expenses.
(ii) Report all warranty-related
information to the certificate holder.
(2) In your application for
certification, identify the company
whose trademark you will use and
describe the arrangements you have
made to meet your requirements under
this section.
(3) You remain responsible for
meeting all the requirements of this
subpart.
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Certifying Emission Families
§ 59.621 Who may apply for a certificate of
conformity?
A certificate of conformity may only
be issued to the manufacturer that
completes the construction of the
portable gasoline container. In unusual
circumstances, upon a petition by a
manufacturer, we may allow another
manufacturer of the container to hold
the certificate of conformity. However,
in order to hold the certificate, the
manufacturer must demonstrate day-today ability to ensure that containers
produced under the certificate will
comply with the requirements of this
subpart.
§ 59.622 What are the general
requirements for obtaining a certificate of
conformity and producing portable gasoline
containers under it?
(a) You must send us a separate
application for a certificate of
conformity for each emission family. A
certificate of conformity for containers
is valid from the indicated effective date
until the end of the production period
for which it is issued. EPA may require
new certification prior to the end of the
production period if EPA finds that
containers are not meeting the standards
in use during their useful life.
(b) The application must be written in
English and contain all the information
required by this subpart and must not
include false or incomplete statements
or information (see § 59.629).
(c) We may ask you to include less
information than we specify in this
subpart, as long as you maintain all the
information required by § 59.628.
(d) You must use good engineering
judgment for all decisions related to
your application (see § 59.603).
(e) An authorized representative of
your company must approve and sign
the application.
(f) See § 59.629 for provisions
describing how we will process your
application.
(g) You may ask us to modify specific
provisions for demonstrating
compliance with the requirements of
this subpart if they cannot be met for
your portable gasoline container. We
may approve your request if we
determine that such a change is
consistent with the intent of this
subpart. We will not approve your
request if it might lead to less effective
emission control or prevent us from
ensuring compliance with the
requirements of this subpart. To make a
request, describe in writing which
provision you are unable to meet, why
you are unable to meet it, and how the
provision should be modified to address
your concern.
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(h) If we approve your application, we
will issue a certificate that will allow
you to produce the containers that you
described in your application for a
specified production period. Certificates
do not allow you to produce containers
that were not described in your
application, unless we approve the
additional containers under § 59.624.
§ 59.623 What must I include in my
application?
This section specifies the information
that must be in your application, unless
we ask you to include less information
under § 59.622(c). We may require you
to provide additional information to
evaluate your application.
(a) Describe the emission family’s
specifications and other basic
parameters of the emission controls. List
each distinguishable configuration in
the emission family. Include
descriptions and part numbers for all
detachable components such as spouts
and caps.
(b) Describe and explain the method
of emission control.
(c) Describe the products you selected
for testing and the reasons for selecting
them.
(d) Describe the test equipment and
procedures that you used, including any
special or alternate test procedures you
used (see § 59.650).
(e) List the specifications of the test
fuel to show that it falls within the
required ranges specified in § 59.650 of
this subpart.
(f) Include the maintenance and use
instructions and warranty information
you will give to the ultimate purchaser
of each new portable gasoline container
(see § 59.613).
(g) Describe your emission control
information label (see § 59.615).
(h) State that your product was tested
as described in the application
(including the test procedures, test
parameters, and test fuels) to show you
meet the requirements of this subpart.
(i) Present emission data to show your
products meet the applicable emission
standards. Where applicable, §§ 59.626
and 59.627 may allow you to submit an
application in certain cases without new
emission data.
(j) Report all test results, including
those from invalid tests or from any
other tests, whether or not they were
conducted according to the test
procedures of §§ 59.650 through 59.653.
We may ask you to send other
information to confirm that your tests
were valid under the requirements of
this subpart.
(k) Unconditionally certify that all the
products in the emission family comply
with the requirements of this subpart,
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other referenced parts of the CFR, and
the Clean Air Act.
(l) Include estimates of U.S.-directed
production volumes.
(m) Include the information required
by other sections of this subpart.
(n) Include other relevant
information, including any additional
information requested by EPA.
(o) Name an agent for service of
process located in the United States.
Service on this agent constitutes service
on you or any of your officers or
employees for any action by EPA or
otherwise by the United States related to
the requirements of this subpart.
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§ 59.624 How do I amend my application
for certification?
Before we issue you a certificate of
conformity, you may amend your
application to include new or modified
configurations, subject to the provisions
of this section. After we have issued
your certificate of conformity, you may
send us an amended application
requesting that we include new or
modified configurations within the
scope of the certificate, subject to the
provisions of this section. You must
amend your application if any changes
occur with respect to any information
included in your application.
(a) You must amend your application
before you take either of the following
actions:
(1) Add a configuration to an emission
family. In this case, the configuration
added must be consistent with other
configurations in the emission family
with respect to the criteria listed in
§ 59.625.
(2) Change a configuration already
included in an emission family in a way
that may affect emissions, or change any
of the components you described in
your application for certification. This
includes production and design changes
that may affect emissions any time
during the portable gasoline containers’
lifetime.
(b) To amend your application for
certification, send the Designated
Compliance Officer the following
information:
(1) Describe in detail the addition or
change in the configuration you intend
to make.
(2) Include engineering evaluations or
data showing that the amended
emission family complies with all
applicable requirements. You may do
this by showing that the original
emission data are still appropriate with
respect to showing compliance of the
amended family with all applicable
requirements.
(3) If the original emission data for the
emission family are not appropriate to
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show compliance for the new or
modified configuration, include new
test data showing that the new or
modified configuration meets the
requirements of this subpart.
(c) We may ask for more test data or
engineering evaluations. You must give
us these within 30 days after we request
them.
(d) For emission families already
covered by a certificate of conformity,
we will determine whether the existing
certificate of conformity covers your
new or modified configuration. You
may ask for a hearing if we deny your
request (see § 59.699).
(e) For emission families already
covered by a certificate of conformity
and you send us a request to amend
your application, you may sell and
distribute the new or modified
configuration before we make a decision
under paragraph (d) of this section,
subject to the provisions of this
paragraph. If we determine that the
affected configurations do not meet
applicable requirements, we will notify
you to cease production of the
configurations and any containers from
the new or modified configuration will
not be considered covered by the
certificate. In addition, we may require
you to recall any affected containers that
you have already distributed, including
those sold to the ultimate purchasers.
Choosing to produce containers under
this paragraph (e) is deemed to be
consent to recall all containers that we
determine do not meet applicable
emission standards or other
requirements and to remedy the
nonconformity at no expense to the
owner. If you do not provide
information required under paragraph
(c) of this section within 30 days, you
must stop producing the new or
modified containers.
§ 59.625 How do I select emission
families?
(a) Divide your product line into
families of portable gasoline containers
that are expected to have similar
emission characteristics throughout the
useful life.
(b) Group containers in the same
emission family if they are the same in
all the following aspects:
(1) Type of material (including
pigments, plasticizers, UV inhibitors, or
other additives).
(2) Production method.
(3) Spout design.
(4) Gasket material/design.
(5) Emission control strategy.
(c) You may subdivide a group of
containers that is identical under
paragraph (b) of this section into
different emission families if you show
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the expected emission characteristics
are different.
(d) You may group containers that are
not identical with respect to the things
listed in paragraph (b) of this section in
the same emission family if you show
that their emission characteristics will
be similar throughout their useful life.
§ 59.626 What emission testing must I
perform for my application for a certificate
of conformity?
This section describes the emission
testing you must perform to show
compliance with the emission standards
in § 59.611.
(a) Test your products using the
procedures and equipment specified in
§§ 59.650 through 59.653.
(b) Select an emission-data unit from
each emission family for testing. You
must test a production sample or a
preproduction product that will
represent actual production. Select the
configuration that is most likely to
exceed (or have emissions nearest to)
the applicable emission standard. For
example, for a family of multilayer
portable gasoline containers, test the
container with the thinnest barrier layer.
Test 3 identical containers.
(c) We may measure emissions from
any of your products from the emission
family. You must supply your products
to us if we choose to perform
confirmatory testing.
(d) You may ask to use emission data
from a previous production period
(carryover) instead of doing new tests,
but only if the emission-data from the
previous production period remains the
appropriate emission-data unit under
paragraph (b) of this section. For
example, you may not carryover
emission data for your family of
containers if you have added a thinnerwalled container than was tested
previously.
(e) We may require you to test a
second unit of the same or different
configuration in addition to the unit
tested under paragraph (b) of this
section.
(f) If you use an alternate test
procedure under § 59.652 and later
testing shows that such testing does not
produce results that are equivalent to
the procedures specified in this subpart,
we may reject data you generated using
the alternate procedure and base our
compliance determination on the later
testing.
§ 59.627 How do I demonstrate that my
emission family complies with evaporative
emission standards?
(a) For purposes of certification, your
emission family is considered in
compliance with an evaporative
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emission standard in § 59.611(a) if the
test results from all portable gasoline
containers in the family that have been
tested show measured emissions levels
that are at or below the applicable
standard.
(b) Your emissions family is deemed
not to comply if any container
representing that family has test results
showing an official emission level above
the standard.
(c) Round the measured emission
level to the same number of decimal
places as the emission standard.
Compare the rounded emission levels to
the emission standard.
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§ 59.628 What records must I keep and
what reports must I send to EPA?
(a) Organize and maintain the
following records:
(1) A copy of all applications and any
summary information you send us.
(2) Any of the information we specify
in § 59.623 that you were not required
to include in your application.
(3) A detailed history of each
emission-data unit. For each emission
data unit, include all of the following:
(i) The emission-data unit’s
construction, including its origin and
buildup, steps you took to ensure that
it represents production containers, any
components you built specially for it,
and all the components you include in
your application for certification.
(ii) All your emission tests, including
documentation on routine and standard
tests, as specified in §§ 59.650 through
59.653, and the date and purpose of
each test.
(iii) All tests to diagnose emissioncontrol performance, giving the date and
time of each and the reasons for the test.
(iv) Any other relevant events or
information.
(4) Production figures for each
emission family divided by assembly
plant.
(5) If you identify your portable
gasoline containers by lot number or
other identification numbers, keep a
record of these numbers for all the
containers you produce under each
certificate of conformity.
(b) Keep data from routine emission
tests (such as test cell temperatures and
relative humidity readings) for one year
after we issue the associated certificate
of conformity. Keep all other
information specified in paragraph (a) of
this section for five years after we issue
your certificate.
(c) Store these records in any format
and on any media, as long as you can
promptly send us organized, written
records in English if we ask for them.
You must keep these records readily
available. We may review them at any
time.
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(d) Send us copies of any
maintenance instructions or
explanations if we ask for them.
(e) Send us an annual warranty report
summarizing by emissions family
successful warranty claims under
§ 59.612, including the reason for the
claim. You must submit the report by
July 1 for the preceding calendar year.
§ 59.629 What decisions may EPA make
regarding my certificate of conformity?
(a) If we determine your application is
complete and shows that the emission
family meets all the requirements of this
subpart and the Act, we will issue a
certificate of conformity for your
emission family for the specified
production period. We may make the
approval subject to additional
conditions.
(b) We may deny your application for
certification if we determine that your
emission family fails to comply with
emission standards or other
requirements of this subpart or the Act.
Our decision may be based on a review
of all information available to us. If we
deny your application, we will explain
why in writing.
(c) In addition, we may deny your
application or suspend, revoke, or void
your certificate if you do any of the
following:
(1) Refuse to comply with any testing
or reporting requirements.
(2) Submit false or incomplete
information.
(3) Render inaccurate any test data.
(4) Deny us from completing
authorized activities despite our
presenting a warrant or court order (see
§ 59.698). This includes a failure to
provide reasonable assistance.
(5) Produce portable gasoline
containers for importation into the
United States at a location where local
law prohibits us from carrying out
authorized activities.
(6) Fail to supply requested
information or amend your application
to include all portable gasoline
containers being produced.
(7) Take any action that otherwise
circumvents the intent of the Act or this
subpart.
(d) If we deny your application or
suspend, revoke, or void your
certificate, you may ask for a hearing
(see § 59.699).
§ 59.630
EPA testing.
We may test any portable gasoline
container subject to the standards of this
subpart.
(a) Certification and production
sample testing. Upon our request, a
manufacturer must supply a prototype
container or a reasonable number of
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production samples to us for
verification testing. These samples will
generally be tested using the full test
procedure of § 59.653.
(b) In-use testing. We may test in-use
containers using the test procedure of
§ 59.653 without preconditioning.
§ 59.650
General testing provisions.
(a) The test procedures of this subpart
are addressed to you as a manufacturer,
but they apply equally to anyone who
does testing for you.
(b) Unless we specify otherwise, the
terms ‘‘procedures’’ and ‘‘test
procedures’’ in this subpart include all
aspects of testing, including the
equipment specifications, calibrations,
calculations, and other protocols and
procedural specifications needed to
measure emissions.
(c) The specification for gasoline to be
used for testing is given in 40 CFR
1065.210. Use the grade of gasoline
specified for general testing. Blend this
grade of gasoline with reagent grade
ethanol in a volumetric ratio of 90.0
percent gasoline to 10.0 percent ethanol.
You may use ethanol that is less pure if
you can demonstrate that it will not
affect your ability to demonstrate
compliance with the applicable
emission standards.
(d) Accuracy and precision of all
temperature measurements must be ±2.2
°C or better.
(e) Accuracy and precision of mass
balances must be sufficient to ensure
accuracy and precision of two percent
or better for emission measurements for
products at the maximum level allowed
by the standard. The readability of the
display may not be coarser than half of
the required accuracy and precision.
§ 59.652
Other procedures.
(a) Your testing. The procedures in
this subpart apply for all testing you do
to show compliance with emission
standards, with certain exceptions listed
in this section.
(b) Our testing. These procedures
generally apply for testing that we do to
determine if your portable gasoline
containers complies with applicable
emission standards. We may perform
other testing as allowed by the Act.
(c) Exceptions. We may allow or
require you to use procedures other than
those specified in this subpart in the
following cases.
(1) You may request to use special
procedures if your portable gasoline
containers cannot be tested using the
specified procedures. We will approve
your request if we determine that it
would produce emission measurements
that represent in-use operation and we
determine that it can be used to show
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compliance with the requirements of the
standard-setting section.
(2) You may ask to use emission data
collected using other procedures, such
as those of the California Air Resources
Board. We will approve this only if you
show us that using these other
procedures do not affect your ability to
show compliance with the applicable
emission standards. This generally
requires emission levels to be far
enough below the applicable emission
standards so that any test differences do
not affect your ability to state
unconditionally that your containers
will meet all applicable emission
standards when tested using the
specified test procedures.
(3) You may request to use alternate
procedures that are equivalent to
allowed procedures, or more accurate or
more precise than allowed procedures.
(d) You may not use other procedures
under paragraph (c) of this section until
we approve your request.
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§ 59.653 How do I test portable gasoline
containers?
You must test the portable gasoline
container as described in your
application, with the applicable spout
and cap attached. Tighten fittings in a
manner representative of how they
would be tightened by a typical user.
(a) Preconditioning for durability.
Complete the following steps at the start
of testing, unless we determine that
omission of one or more of these
durability steps will not affect the
emissions from your container.
(1) Pressure cycling. Perform a
pressure test by sealing the container
and cycling it between +13.8 and ¥1.7
kPa (+2.0 and ¥0.5 psig) and back to
+13.8 kPa for 10,000 cycles at a rate of
60 seconds per cycle.
(2) UV exposure. Perform a sunlightexposure test by exposing the container
to an ultraviolet light of at least 24 W/
m2 (0.40 W-hr/m2/min) on the container
surface for at least 450 hours.
Alternatively, the container may be
exposed to direct natural sunlight for an
equivalent period of time, as long as you
ensure that the container is exposed to
at least 450 daylight hours.
(3) Slosh testing. Perform a slosh test
by filling the portable gasoline container
to 40 percent of its capacity with the
fuel specified in paragraph (e) of this
section and rocking it at a rate of 15
cycles per minute until you reach one
million total cycles. Use an angle
deviation of +15° to ¥15° from level.
This test must be performed at a
temperature of 28 °C ± 5°C.
(4) Spout actuation. Perform the
following spout actuation and inversion
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steps at the end on the slosh testing, and
at the end of the preconditioning soak.
(i) Perform one complete actuation/
inversion cycle per day for ten days.
(ii) One actuation/inversion cycle
consists of the following steps:
(A) Remove and replace the spout to
simulate filling the container.
(B) Slowly invert the container and
keep it inverted for at least 5 seconds to
ensure that the spout and mechanisms
become saturated with fuel. Any fuel
leaking from any part of the container
will denote a leak and will be reported
as part of certification. Once completed,
place the container on a flat surface in
the upright position.
(C) Actuate the spout by fully opening
and closing without dispensing fuel.
The spout must return to the closed
position without the aid of the operator
(e.g., pushing or pulling the spout
closed). Repeat for a total of 10
actuations. If at any point the spout fails
to return to the closed position, the
container fails the test.
(D) Repeat the step contained in
paragraph (a)(4)(ii)(B) of this section
(i.e., the inversion step).
(E) Repeat the steps contained in
paragraph (a)(4)(ii)(C) of this section
(i.e., ten actuations).
(b) Preconditioning fuel soak.
Complete the following steps before a
diurnal emission test: (1) Fill the
portable gasoline container with the
specified fuel to its nominal capacity,
seal it using the spout, and allow it to
soak at 28 ±5 °C for at least 20 weeks.
You are not required to soak the
container for more than 20 weeks unless
it has been determined that a longer
soak period is needed to achieve a
stabilized emissions rate. Alternatively,
the container may be soaked for a
shorter period of time at a higher
temperature if you can show that the
hydrocarbon permeation rate has
stabilized. You may count the time of
the slosh testing as part of the 20 weeks.
(2) Pour the fuel out of the container
and immediately refill to 50 percent of
nominal capacity. Be careful to not spill
any fuel on the container. Wipe the
outside of the container as needed to
remove any liquid fuel that may have
spilled on it.
(3) Seal the container using the spout
and cap assemblies that will used to seal
the openings in a production container.
Leave other openings on the container
(such as vents) open unless they are
automatically closing and unlikely for
the user to leave open during typical
storage.
(c) Reference container. A reference
tank is required to correct for buoyancy
effects that may occur during testing.
Prepare the reference tank as follows:
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(1) Obtain a second tank that is
identical to the test tank. You may not
use a tank that has previously contained
fuel or any other contents that might
affect the stability of its mass.
(2) Fill the reference tank with enough
dry sand (or other inert material) so that
the mass of the reference tank is
approximately the same as the test tank
when filled with fuel. Use good
engineering judgment to determine how
similar the mass of the reference tank
needs to be to the mass of the test tank
considering the performance
characteristics of your balance.
(3) Ensure that the sand (or other inert
material) is dry. This may require
heating the tank or applying a vacuum
to it.
(4) Seal the tank.
(d) Diurnal test run. To run the test,
take the steps specified in this
paragraph (d) for a portable gasoline
container that was preconditioned as
specified in paragraph (a) of this
section.
(1) Stabilize the fuel temperature
within the portable gasoline container at
22.2 °C. Vent the container at this point
to relieve any positive or negative
pressure that may have developed
during stabilization.
(2) Weigh the sealed reference
container and record the weight. Place
the reference on the balance and tare it
so that it reads zero. Place the sealed
test portable gasoline container on the
balance and record the difference
between the test container and the
reference container. This value is Minitial
Take this measurement within 8 hours
of filling the test container with fuel as
specified in paragraph (b)(2) of this
section.
(2) Immediately place the portable
gasoline container within a well
ventilated, temperature-controlled room
or enclosure. Do not spill or add any
fuel.
(3) Close the room or enclosure.
(4) Follow the temperature profile in
the following table for all portable
gasoline containers. Use good
engineering judgment to follow this
profile as closely as possible. You may
use linearly interpolated temperatures
or a spline fit for temperatures between
the hourly setpoints.
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TABLE 1 OF § 59.653.—DIURNAL TEM- container durability cycles (i.e., the
PERATURE PROFILE FOR PORTABLE pressure cycling, UV exposure, and
slosh testing) specified in this section.
GASOLINE CONTAINERS
Time (hours)
For other containers, you may
demonstrate compliance without
performing the durability cycles
specified in this section only if we
approve it after you have presented data
clearly demonstrating that the cycle or
cycles do not negatively impact the
22.2 permeation rate of the materials used in
22.5 the containers.
Ambient Temperature (C)
Profile for
Portable
Gasoline
Containers
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0 ............................................
1 ............................................
2 ............................................
3 ............................................
4 ............................................
5 ............................................
6 ............................................
7 ............................................
8 ............................................
9 ............................................
10 ..........................................
11 ..........................................
12 ..........................................
13 ..........................................
14 ..........................................
15 ..........................................
16 ..........................................
17 ..........................................
18 ..........................................
19 ..........................................
20 ..........................................
21 ..........................................
22 ..........................................
23 ..........................................
24 ..........................................
24.2
26.8
29.6
31.9
33.9
35.1
35.4
35.6
35.3
34.5
33.2
31.4
29.7
28.2
27.2
26.1
25.1
24.3
23.7
23.3
22.9
22.6
22.2
(5) At the end of the diurnal period,
retare the balance using the reference
container and weigh the portable
gasoline container. Record the
difference in mass between the
reference container and the test. This
value is Mfinal
(6) Subtract Mfinal from Minitial; and
divide the difference by the nominal
capacity of the container (using at least
three significant figures) to calculate the
g/gallon/day emission rate:
Emission rate = (Minitial¥Mfinal)/
(nominal capacity)/(one day)
(7) Round your result to the same
number of decimal places as the
emission standard.
(8) Instead of determining emissions
by weighing the container before and
after the diurnal temperature cycle, you
may place the container in a SHED
meeting the specifications of 40 CFR
86.107–96(a)(1) and measure emissions
directly. Immediately following the
stabilization in paragraph (d)(1) of this
section, purge the SHED and follow the
temperature profile from paragraph
(d)(4) of this section. Start measuring
emissions when you start the
temperature profile.
(e) For metal containers, you may
demonstrate for certification that your
portable gasoline containers comply
with the evaporative emission standards
without performing the pre-soak or
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Special Compliance Provisions
§ 59.660
Exemption from the standards.
In certain circumstances, we may
exempt portable gasoline containers
from the evaporative emission standards
and requirements of § 59.611 and the
prohibitions and requirements of
§ 59.602. You do not need an exemption
for any containers that you own but do
not sell, offer for sale, introduce or
deliver for introduction into U.S.
commerce, or import into the United
States. Submit your request for an
exemption to the Designated
Compliance Officer.
(a) Portable gasoline containers that
are intended for export only and are in
fact exported are exempt provided they
are clearly labeled as being for export
only. Keep records for five years of all
portable gasoline containers that you
manufacture for export. Any
introduction into U.S. commerce for any
purpose other than export is considered
to be a violation of § 59.602 by the
manufacturer. You do not need to
request this exemption.
(b) You may ask us to exempt portable
gasoline containers that you will
purchase, sell, or distribute for the sole
purpose of testing them.
(c) You may ask us to exempt portable
gasoline containers for the purpose of
national security, as long as your
request is endorsed by an agency of the
federal government responsible for
national defense. In your request,
explain why you need the exemption.
(d) You may ask us to exempt
containers that are designed and
marketed solely for rapidly refueling
racing applications which are designed
to create a leak proof seal with the target
tank or are designed to connect with a
receiver installed on the target tank.
This exemption is generally intended
for containers used to rapidly refuel a
race car during a pit stop and similar
containers. In your request, explain how
why these containers are unlikely to be
used for nonracing applications. We
may limit these exemptions to those
applications that are allowed to use
gasoline exempted under 40 CFR
80.200.
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(e) EPA may impose reasonable
conditions on any exemption, including
a limit on the number of containers that
are covered by an exemption.
§ 59.662 What temporary provisions
address hardship due to unusual
circumstances?
(a) After considering the
circumstances, we may permit you to
introduce into commerce exempt you
from the evaporative emission standards
and requirements of § 59.611 of this
subpart and the prohibitions and
requirements of § 59.602 for specified
portable gasoline containers that do not
comply with emission standards if all
the following conditions apply:
(1) Unusual circumstances that are
clearly outside your control and that
could not have been avoided with
reasonable discretion prevent you from
meeting requirements from this subpart.
(2) You exercised prudent planning
and were not able to avoid the violation;
you have taken all reasonable steps to
minimize the extent of the
nonconformity.
(3) Not having the exemption will
jeopardize the solvency of your
company.
(4) No other allowances are available
under the regulations in this chapter to
avoid the impending violation.
(b) To apply for an exemption, you
must send the Designated Officer a
written request as soon as possible
before you are in violation. In your
request, show that you meet all the
conditions and requirements in
paragraph (a) of this section.
(c) Include in your request a plan
showing how you will meet all the
applicable requirements as quickly as
possible.
(d) You must give us other relevant
information if we ask for it.
(e) We may include reasonable
additional conditions on an approval
granted under this section, including
provisions to recover or otherwise
address the lost environmental benefit
or paying fees to offset any economic
gain resulting from the exemption.
(f) We may approve extensions of up
to one year. We may review and revise
an extension as reasonable under the
circumstances.
(g) Add a legible label, written in
block letters in English, to a readily
visible part of each container exempted
under this section. This label must
prominently include at least the
following items:
(1) Your corporate name and
trademark.
(2) The statement ‘‘EXEMPT UNDER
40 CFR 59.662.’’.
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§ 59.663 What are the provisions for
extending compliance deadlines for
manufacturers under hardship?
(a) After considering the
circumstances, we may extend the
compliance deadline for you to meet
new emission standards, as long as you
meet all the conditions and
requirements in this section.
(b) To apply for an extension, you
must send the Designated Compliance
Officer a written request. In your
request, show that all the following
conditions and requirements apply:
(1) You have taken all possible
business, technical, and economic steps
to comply.
(2) Show that the burden of
compliance costs prevents you from
meeting the requirements of this subpart
by the required compliance date.
(3) Not having the exemption will
jeopardize the solvency of your
company.
(4) No other allowances are available
under the regulations in this subpart to
avoid the impending violation.
(c) In describing the steps you have
taken to comply under paragraph (b)(1)
of this section, include at least the
following information:
(1) Describe your business plan,
showing the range of projects active or
under consideration.
(2) Describe your current and
projected financial standing, with and
without the burden of complying in full
with the applicable regulations in this
subpart by the required compliance
date.
(3) Describe your efforts to raise
capital to comply with regulations in
this subpart.
(4) Identify the engineering and
technical steps you have taken or plan
to take to comply with regulations in
this subpart.
(5) Identify the level of compliance
you can achieve. For example, you may
be able to produce containers that meet
a somewhat less stringent emission
standard than the regulations in this
subpart require.
(d) Include in your request a plan
showing how you will meet all the
applicable requirements as quickly as
possible.
(e) You must give us other relevant
information if we ask for it.
(f) An authorized representative of
your company must sign the request and
include the statement: ‘‘All the
information in this request is true and
accurate, to the best of my knowledge.’’.
(g) Send your request for this
extension at least nine months before
the relevant deadline.
(h) We may include reasonable
requirements on an approval granted
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under this section, including provisions
to recover or otherwise address the lost
environmental benefit. For example, we
may require that you meet a less
stringent emission standard.
(i) We may approve extensions of up
to one year. We may review and revise
an extension as reasonable under the
circumstances.
(j) Add a permanent, legible label,
written in block letters in English, to a
readily visible part of each container
exempted under this section. This label
must prominently include at least the
following items:
(1) Your corporate name and
trademark.
(2) The statement ‘‘EXEMPT UNDER
40 CFR 59.663.’’.
§ 59.664 What are the requirements for
importing portable gasoline containers into
the United States?
As specified in this section, we may
require you to post a bond if you import
into the U.S. containers that are subject
to the standards of this subpart. See
paragraph (f) of this section for the
requirements related to importing
containers that have been certified by
someone else.
(a) Prior to importing containers into
the U.S., we may require you to post a
bond to cover any potential enforcement
actions under the Clean Air Act if you
cannot demonstrate to us that you have
assets of an appropriate liquidity readily
available in the United States with a
value equal to the retail value of the
containers that you will import during
the calendar year.
(b) We may set the value of the bond
up to five dollars per container.
(c) You may meet the bond
requirements of this section by
obtaining a bond from a third-party
surety that is cited in the U.S.
Department of Treasury Circular 570,
‘‘Companies Holding Certificates of
Authority as Acceptable Sureties on
Federal Bonds and as Acceptable
Reinsuring Companies’’ (https://
www.fms.treas.gov/c570/
c570.html#certified).
(d) If you forfeit some or all of your
bond in an enforcement action, you
must post any appropriate bond for
continuing importation within 90 days
after you forfeit the bond amount.
(e) You will forfeit the proceeds of the
bond posted under this section if you
need to satisfy any United States
administrative final order or judicial
judgment against you arising from your
conduct in violation of this subpart.
(f) This paragraph (f) applies if you
import for resale containers that have
been certified by someone else. You and
the certificate holder are each
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responsible for compliance with the
requirements of this subpart and the
Clean Air Act. No bond is required
under this section if either you or the
certificate holder meet the conditions in
paragraph (a) of this section. Otherwise,
the importer must comply with the
bond requirements of this section.
Definitions and Other Reference
Information
§ 59.680 What definitions apply to this
subpart?
The following definitions apply to
this subpart. The definitions apply to all
subparts unless we note otherwise. All
undefined terms have the meaning the
Act gives to them. The definitions
follow:
Act means the Clean Air Act, as
amended, 42 U.S.C. 7401—7671q.
Adjustable parameter means any
device, system, or element of design that
someone can adjust and that, if
adjusted, may affect emissions. You may
ask us to exclude a parameter if you
show us that it will not be adjusted in
use in a way that affects emissions.
Certification means the process of
obtaining a certificate of conformity for
an emission family that complies with
the emission standards and
requirements in this subpart.
Certified emission level means the
highest official emission level in an
emission family.
Configuration means a unique
combination of hardware (material,
geometry, and size) and calibration
within an emission family. Units within
a single configuration differ only with
respect to normal production variability.
Container means portable gasoline
container.
Designated Compliance Officer means
the Manager, Engine Programs Group
(6405–J), U.S. Environmental Protection
Agency, 1200 Pennsylvania Ave., NW.,
Washington, DC 20460.
Designated Enforcement Officer
means the Director, Air Enforcement
Division (2242A), U.S. Environmental
Protection Agency, 1200 Pennsylvania
Ave., NW.,Washington, DC 20460.
Emission-control system means any
device, system, or element of design that
controls or reduces the regulated
evaporative emissions from.
Emission-data unit means a portable
gasoline container that is tested for
certification. This includes components
tested by EPA.
Emission-related maintenance means
maintenance that substantially affects
emissions or is likely to substantially
affect emission deterioration.
Emission family has the meaning
given in § 59.625.
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Evaporative means relating to fuel
emissions that result from permeation of
fuel through the portable gasoline
container materials and from ventilation
of the container.
Good engineering judgment means
judgments made consistent with
generally accepted scientific and
engineering principles and all available
relevant information. See § 59.603 for
the administrative process we use to
evaluate good engineering judgment.
Hydrocarbon (HC) means total
hydrocarbon (THC).
Manufacture means the physical and
engineering process of designing and/or
constructing a portable gasoline
container.
Manufacturer means any person who
manufactures a portable gasoline
container for sale in the United States.
Nominal capacity means the expected
volumetric working capacity of a
container.
Official emission result means the
measured emission rate for an emissiondata unit.
Portable gasoline container means
any reusable container designed and
marketed (or otherwise intended) for
use by consumers for receiving,
transporting, storing, and dispensing
gasoline. For the purpose of this
subpart, all portable fuel containers that
are red in color are deemed to be
portable gasoline containers, regardless
of how they are labeled or marketed.
Portable fuel containers that are not red
in color and are clearly and
permanently labeled for diesel fuel or
kerosene only and not for use with
gasoline are not portable gasoline
containers.
Production period means the period
in which a portable gasoline container
will be produced under a certificate of
conformity. The maximum production
period is five years.
Revoke means to terminate the
certificate or an exemption for an
emission family. If we revoke a
certificate or exemption, you must apply
for a new certificate or exemption before
continuing to introduce the affected
containers into commerce. This does not
apply to containers you no longer
possess.
Round has the meaning given in 40
CFR 1065.1001.
Sealed means lacking openings that
would allow liquid or vapor to escape
to the atmosphere under normal
operating pressures.
Suspend means to temporarily
discontinue the certificate or an
exemption for an emission family. If we
suspend a certificate, you may not
introduce into commerce portable
gasoline containers from that emission
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family unless we reinstate the certificate
or approve a new one. If we suspend an
exemption, you may not introduce into
commerce containers that were
previously covered by the exemption
unless we reinstate the exemption.
Test sample means the collection of
portable gasoline containers selected
from the population of an emission
family for emission testing. This may
include testing for certification,
production-line testing, or in-use
testing.
Test unit means a portable gasoline
container in a test sample.
Total hydrocarbon means the
combined mass of organic compounds
measured by the specified procedure for
measuring total hydrocarbon, expressed
as a hydrocarbon with a hydrogen-tocarbon mass ratio of 1.85:1.
Ultimate purchaser means, with
respect to any portable gasoline
container, the first person who in good
faith purchases such a container for
purposes other than resale.
Ultraviolet light means
electromagnetic radiation with a
wavelength between 300 and 400
nanometers.
United States means the States, the
District of Columbia, the
Commonwealth of Puerto Rico, the
Commonwealth of the Northern Mariana
Islands, Guam, American Samoa, and
the U.S. Virgin Islands.
U.S.-directed production volume
means the amount of portable gasoline
containers, subject to the requirements
of this subpart, produced by a
manufacturer for which the
manufacturer has a reasonable
assurance that sale was or will be made
to ultimate purchasers in the United
States.
Useful life means the period during
which a portable gasoline container is
required to comply with all applicable
emission standards. See § 59.611.
Void means to invalidate a certificate
or an exemption ab initio (i.e.
retroactively). Portable gasoline
containers introduced into U.S.
commerce under the voided certificate
or exemption is a violation of this
subpart, whether or not they were
introduced before the certificate or
exemption was voided.
We (us, our) means the Administrator
of the Environmental Protection Agency
and any authorized representatives.
§ 59.685 What symbols, acronyms, and
abbreviations does this subpart use?
The following symbols, acronyms,
and abbreviations apply to this subpart:
CFR Code of Federal Regulations.
EPA Environmental Protection Agency.
HC hydrocarbon.
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NIST National Institute of Standards and
Technology.
THC total hydrocarbon.
U.S.C. United States Code.
§ 59.695 What provisions apply to
confidential information?
(a) Clearly show what you consider
confidential by marking, circling,
bracketing, stamping, or some other
method.
(b) We will store your confidential
information as described in 40 CFR part
2. Also, we will disclose it only as
specified in 40 CFR part 2. This applies
both to any information you send us and
to any information we collect from
inspections, audits, or other site visits.
(c) If you send us a second copy
without the confidential information,
we will assume it contains nothing
confidential whenever we need to
release information from it.
(d) If you send us information without
claiming it is confidential, we may make
it available to the public without further
notice to you, as described in 40 CFR
2.204.
§ 59.697
State actions.
The provisions in this subpart do not
preclude any State or any political
subdivision of a State from:
(a) Adopting and enforcing any
emission standard or limitation
applicable to anyone subject to the
provisions of this part; or
(b) Requiring the regulated entity to
obtain permits, licenses, or approvals
prior to initiating construction,
modification, or operation of a facility
for manufacturing a consumer product.
§ 59.698 May EPA enter my facilities for
inspections?
(a) We may inspect your portable
gasoline containers, testing,
manufacturing processes, storage
facilities (including port facilities for
imported containers or other relevant
facilities), or records, as authorized by
the Act, to enforce the provisions of this
subpart. Inspectors will have
authorizing credentials and will limit
inspections to reasonable times—
usually, normal operating hours.
(b) If we come to inspect, we may or
may not have a warrant or court order.
(1) If we do not have a warrant or
court order, you may deny us entry.
(2) If we have a warrant or court
order, you must allow us to enter the
facility and carry out the activities it
describes.
(c) We may seek a warrant or court
order authorizing an inspection
described in this section, whether or not
we first tried to get your permission to
inspect.
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(d) We may select any facility to do
any of the following:
(1) Inspect and monitor any aspect of
portable gasoline container
manufacturing, assembly, storage, or
other procedures, and any facilities
where you do them.
(2) Inspect and monitor any aspect of
test procedures or test-related activities,
including test container selection,
preparation, durability cycles, and
maintenance and verification of your
test equipment’s calibration.
(3) Inspect and copy records or
documents related to assembling,
storing, selecting, and testing a
container.
(4) Inspect and photograph any part or
aspect of containers or components use
for assembly.
(e) You must give us reasonable help
without charge during an inspection
authorized by the Act. For example, you
may need to help us arrange an
inspection with the facility’s managers,
including clerical support, copying, and
translation. You may also need to show
us how the facility operates and answer
other questions. If we ask in writing to
see a particular employee at the
inspection, you must ensure that he or
she is present (legal counsel may
accompany the employee).
(f) If you have facilities in other
countries, we expect you to locate them
in places where local law does not keep
us from inspecting as described in this
section. We will not try to inspect if we
learn that local law prohibits it, but we
may suspend your certificate if we are
not allowed to inspect.
§ 59.699
How do I request a hearing?
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(a) You may request a hearing under
certain circumstances, as described
elsewhere in this subpart. To do this,
you must file a written request with the
Designated Compliance Officer,
including a description of your
objection and any supporting data,
within 30 days after we make a
decision.
(b) For a hearing you request under
the provisions of this subpart, we will
approve your request if we find that
your request raises a substantial factual
issue.
(c) If we agree to hold a hearing, we
will use the procedures specified in 40
CFR part 1068, subpart G.
PART 80—REGULATION OF FUELS
AND FUEL ADDITIVES
3. The authority citation for part 80 is
revised to read as follows:
Authority: 42 U.S.C. 7414, 7521(1), 7545
and 7601(a).
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Subpart D—[Amended]
4. Section 80.41 is amended by
redesignating paragraph (e) as paragraph
(e)(1), redesignating paragraph (f) as
paragraph (f)(1), and adding paragraphs
(e)(2) and (f)(2) to read as follows:
§ 80.41 Standards and requirements for
compliance.
*
*
*
*
*
(e) * * *
(2) Beginning January 1, 2011, or
January 1, 2015 for approved small
refiners under § 80.1340, the toxic air
pollutants emissions performance
reduction and benzene content specified
in paragraph (e)(1) of this section shall
apply only to reformulated gasoline that
is not subject to the benzene standard of
§ 80.1230, pursuant to the provisions of
§ 80.1235. Beginning January 1, 2007, or
January 1, 2008 for approved small
refiners under § 80.235, the NOX
emissions performance reduction
specified in paragraph (e)(1) of this
section shall no longer apply.
(f) * * *
(2) Beginning January 1, 2011, or
January 1, 2015 for approved small
refiners under § 80.1340, the toxic air
pollutants emissions performance
reduction and benzene content specified
in paragraph (f)(1) of this section shall
apply only to reformulated gasoline that
is not subject to the benzene standard of
§ 80.1230, pursuant to the provisions of
§ 80.1235. Beginning January 1, 2007, or
January 1, 2008 for approved small
refiners under § 80.235, the NOX
emissions performance reduction
specified in paragraph (f)(1) of this
section shall no longer apply.
*
*
*
*
*
5. Section 80.101 is amended by
revising paragraph (c)(2) to read as
follows:
§ 80.101 Standards applicable to refiners
and importers.
*
*
*
*
(c) * * *
(2) Beginning January 1, 1998, each
refiner and importer shall be subject to
the Complex Model standards for each
averaging period. However beginning
January 1, 2011, or January 1, 2015 for
approved small refiners under
§ 80.1340, such annual average exhaust
toxics standard shall apply only to
conventional gasoline that is not subject
to the benzene standard of § 80.1230,
pursuant to the provisions of § 80.1235.
Beginning January 1, 2007, or January 1,
2008 for approved small refiners under
§ 80.235, the annual average NOX
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Subpart F—[Amended]
6. Section 80.128 is amended by
revising paragraph (a) to read as follows:
§ 80.128 Agreed upon procedures for
refiners and importers.
*
*
*
*
*
(a) Read the refiner’s or importer’s
reports filed with EPA for the previous
year as required by §§ 80.75, 80.83(g),
80.105, 80.990 and 80.1354.
*
*
*
*
*
Subpart J—[Amended]
7. Section 80.815 is amended by
redesignating paragraph (d)(1) as
paragraph (d)(1)(i) and adding
paragraph (d)(1)(ii) to read as follows:
§ 80.815 What are the gasoline toxics
performance requirements for refiners and
importers?
*
*
*
*
*
(d) * * *
(1) * * *
(ii) Beginning January 1, 2011, or
January 1, 2015 for approved small
refiners under § 80.1340, the gasoline
toxics performance requirements of this
subpart shall apply only to gasoline that
is not subject to the benzene standard of
§ 80.1230, pursuant to the provisions of
§ 80.1235.
*
*
*
*
*
8. Section 80.1035 is amended by
adding paragraph (h) to read as follows:
§ 80.1035 What are the attest engagement
requirements for gasoline toxics
compliance applicable to refiners and
importers?
*
Subpart E—[Amended]
*
emissions standard section shall no
longer apply.
*
*
*
*
*
*
*
*
*
(h) Beginning January 1, 2011, or
January 1, 2015 for approved small
refiners per § 80.1340, the requirements
of this section shall apply only to
gasoline that is not subject to the
benzene standard of § 80.1230, pursuant
to the provisions of § 80.1235.
9. Subpart L is added to read as
follows:
Subpart L—Gasoline Benzene
Sec.
80.1200—80.1219 [Reserved]
General Information
80.1220 What are the implementation dates
for the gasoline benzene program?
80.1225 Who must register with EPA under
the gasoline benzene program?
Gasoline Benzene Requirements
80.1230 What are the gasoline benzene
requirements for refiners and importers?
80.1235 What gasoline is subject to the
benzene requirements of this subpart?
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80.1236 What requirements apply to
California gasoline?
80.1238 How is a refinery’s or importer’s
annual average benzene concentration
determined?
80.1240 How is a refinery’s or importer’s
compliance with the gasoline benzene
requirements of this subpart determined?
80.1415 What penalties apply under the
gasoline benzene program?
Averaging, Banking and Trading (ABT)
Program
80.1270 Who may generate benzene credits
under the ABT program?
80.1275 How are early benzene credits
generated?
80.1280 How are refinery benzene baselines
calculated?
80.1285 How does a refiner apply for a
benzene baseline?
80.1290 How are benzene credits generated
in 2011 and beyond?
80.1295 How are gasoline benzene credits
used?
Subpart L—Gasoline Benzene
Hardship Provisions
80.1335 Can a refiner seek temporary relief
from the requirements of this subpart?
80.1336 What if a refiner or importer cannot
produce gasoline conforming to the
requirements of this subpart?
Small Refiner Provisions
80.1338 What is the definition of a small
refiner for the purpose of the gasoline
benzene requirements of this subpart?
80.1339 Who is not eligible for the
provisions for small refiners?
80.1340 How does a refiner obtain approval
as a small refiner?
80.1342 What compliance options are
available to small refiners under this
subpart?
80.1344 What provisions are available to a
large refiner that acquires one or more of
a small refiner’s refineries?
Sampling, Testing and Retention
Requirements
80.1347 What are the sampling and testing
requirements for refiners and importers?
80.1348 What gasoline sample retention
requirements apply to refiners and
importers?
Recordkeeping and Reporting Requirements
80.1350 What records must be kept?
80.1352 What are the pre-compliance
reporting requirements for the gasoline
benzene program?
80.1354 What are the reporting
requirements for the gasoline benzene
program?
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Attest Engagements
80.1375 What are the attest engagement
requirements for gasoline benzene
compliance?
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§§ 80.1200–80.1219
[Reserved]
General Information
§ 80.1220 What are the implementation
dates for the gasoline benzene program?
(a) Benzene standard. (1) Effective
with the annual averaging period
beginning January 1, 2011, gasoline
produced by a refiner at each refinery,
or imported into an import facility, must
meet the benzene standard specified in
§ 80.1230, except as otherwise
specifically provided for in this subpart.
(2) Approved small refiners under
§ 80.1340 may defer meeting the
benzene standard specified in § 80.1230
until January 1, 2015 as described in
§ 80.1342.
(b) Early credit generation. (1)
Beginning June 1, 2007, each refinery
which has an approved benzene
baseline per § 80.1285 may generate
early benzene credits in accordance
with the provisions of § 80.1275.
(2) Early benzene credits may be
generated through the end of the
averaging period ending December 31,
2010.
(3) Early benzene credits may be
generated through the end of the
averaging period ending December 31,
2014 for approved small refiners under
§ 80.1340.
(c) Standard credit generation. (1)
Effective with the annual averaging
period beginning January 1, 2011, a
refiner for any of its refineries or an
importer for its imported gasoline, may
generate benzene credits in accordance
with the provisions of § 80.1290.
(2) Effective with the annual
averaging period beginning January 1,
2015, an approved small refiner under
§ 80.1340, for any of its refineries, may
generate benzene credits in accordance
with the provisions of § 80.1290.
§ 80.1225 Who must register with EPA
under the gasoline benzene program?
Violations and Penalties
80.1400 What acts are prohibited under the
gasoline benzene program?
80.1405 What evidence may be used to
determine compliance with the
prohibitions and requirements of this
subpart and liability for violations of this
subpart?
80.1410 Who is liable for violations under
the gasoline benzene program?
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Foreign Refiners
80.1420 What are the additional
requirements under this subpart for
gasoline produced at foreign refineries?
(a) Refiners and importers that are
registered by EPA under § 80.76,
§ 80.103, § 80.190, or § 80.810 are
deemed to be registered for purposes of
this subpart.
(b) Refiners and importers subject to
the requirements in § 80.1230 that are
not registered by EPA under § 80.76,
§ 80.103, § 80.190 or § 80.810 shall
provide to EPA the information required
in § 80.76 by September 30, 2010, or not
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15939
later than three months in advance of
the first date that such person produces
or imports gasoline, whichever is later.
(c) Refiners that plan to generate early
credits under § 80.1275 and that are not
registered by EPA under § 80.76,
§ 80.103, § 80.190, or § 80.810 must
provide to EPA the information required
in § 80.76 not later than 60 days prior
to the end of the first year of credit
generation.
Gasoline Benzene Requirements
§ 80.1230 What are the gasoline benzene
requirements for refiners and importers?
(a)(1) Except as specified in paragraph
(b) of this section, a refinery’s or
importer’s average gasoline benzene
concentration in any averaging period
shall not exceed 0.62 percent by volume
using conventional rounding
methodology.
(2) Compliance with the standard
specified in paragraph (a)(1) of this
section, or creation of a deficit in
accordance with paragraph (b) of this
section, is determined in accordance
with § 80.1240.
(3) The averaging period for achieving
compliance with the requirement of
paragraph (a)(1) of this section is
January 1 through December 31 of each
calendar year, beginning January 1,
2011, or beginning January 1, 2015 for
approved small refiners under
§ 80.1340.
(4) Refinery grouping per § 80.101(h)
does not apply to compliance with the
gasoline benzene requirement specified
in this paragraph (a).
(5) Gasoline produced at foreign
refineries that is subject to the gasoline
benzene requirements per § 80.1235
shall be included in the importer’s
compliance determination, except as
provided in § 80.1420.
(b) Deficit carry-forward. (1) A
refinery or importer creates a benzene
deficit for a given averaging period
when its compliance benzene value, per
§ 80.1240, is greater than the benzene
standard specified in paragraph (a) of
this section.
(2) A refinery or importer may carry
the benzene deficit forward to the
calendar year following the year the
benzene deficit is created but only if no
deficit had been previously carried
forward a deficit to the year the deficit
is created. If a refinery or importer
carries forward, the following
provisions apply in the second year:
(i) The refinery or importer must
achieve compliance with the benzene
standard specified in paragraph (a) of
this section.
(ii) The refinery or importer must
achieve further reductions in its
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gasoline benzene concentrations
sufficient to offset the benzene deficit of
the previous year.
(iii) Benzene credits may be used, per
§ 80.1295, to meet the requirements of
paragraphs (b)(2)(i) and (ii) of this
section.
(3) In the case of an approved
hardship under § 80.1335 or § 80.1336,
EPA may allow a briefly extended
period of deficit carry-forward.
(c) Oxygenate blenders, butane
blenders and refiners that produce
gasoline from transmix. (1)(i) Refiners
and oxygenate blenders that only blend
butane or oxygenate into gasoline
downstream of the refinery that
produced the gasoline or the import
facility where the gasoline was
imported, are not subject to the
requirements of § 80.1230 for such
gasoline.
(ii) Refiners that produce gasoline by
separating gasoline from transmix are
not subject to the requirements of
§ 80.1230 for this gasoline.
(2) Any refiner under paragraph (c)(1)
of this section that adds any blendstock
or feedstock other than, or in addition
to, oxygenate and/or butane into
gasoline downstream of the refinery that
produced the gasoline or the import
facility where the gasoline was
imported, or into transmix, or into
gasoline produced from transmix, is
subject to the requirements of § 80.1230
for this blendstock or feedstock.
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§ 80.1235 What gasoline is subject to the
benzene requirements of this subpart?
For the purposes of determining
compliance with the requirements of
§ 80.1230, all reformulated gasoline,
RBOB, and conventional gasoline or
gasoline blending stock per § 80.101(d)
are collectively ‘‘gasoline.’’ Unless
otherwise specified, all of a refinery’s or
importer’s gasoline is subject to the
standards and requirements of
§ 80.1230, with the following
exceptions:
(a) Gasoline that is used to fuel
aircraft, racing vehicles or racing boats
that are used only in sanctioned racing
events, provided that:
(1) Product transfer documents
associated with such gasoline, and any
pump stand from which such gasoline
is dispensed, identify the gasoline either
as gasoline that is restricted for use in
aircraft, or as gasoline that is restricted
for use in racing motor vehicles or
racing boats that are used only in
sanctioned events;
(2) The gasoline is completely
segregated from all other gasoline
throughout production, distribution and
sale to the ultimate consumer; and
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(3) The gasoline is not made available
for use as motor vehicle gasoline, or
dispensed for use in motor vehicles,
except for motor vehicles used only in
sanctioned racing events.
(b) California gasoline, as defined in
§ 80.1236.
(c) Gasoline that is exported for sale
outside the U.S.
(d) Gasoline used for research,
development or testing purposes if it is
exempted for these purposes under the
reformulated gasoline and anti-dumping
programs, as applicable.
(e) Gasoline produced pursuant to
§ 80.1230(c)(1).
§ 80.1236 What requirements apply to
California gasoline?
(a) Definition. For purposes of this
subpart, California gasoline means any
gasoline designated by the refiner or
importer as for use only in California
and that is actually used in California.
(b) California gasoline exemption.
California gasoline that complies with
all the requirements of this section is
exempt from the requirements in
§ 80.1230.
(c) Requirements for California
gasoline. The following requirements
apply to California gasoline:
(1) Each batch of California gasoline
must be designated as such by its refiner
or importer.
(2) Designated California gasoline
must be kept segregated from gasoline
that is not California gasoline at all
points in the distribution system.
(3) Designated California gasoline
must ultimately be used in the State of
California and not used elsewhere in the
United States.
(4) In the case of California gasoline
produced outside the State of California,
the transferors and transferees must
meet the product transfer document
requirements under § 80.81(g).
(5) Gasoline that is ultimately used in
any part of the United States outside of
the State of California must comply with
the requirements specified in § 80.1230,
regardless of any designation as
California gasoline.
§ 80.1238 How is a refinery’s or importer’s
annual average benzene concentration
determined?
(a) The annual average benzene
concentration of gasoline produced at a
refinery or imported by an importer for
the applicable averaging period is
calculated according to the following
equation:
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n
∑(V × B )
i
Bavg =
i
i =1
n
∑V
i
i =1
Where:
Bavg = Annual average benzene
concentration (volume percent
benzene).
i = Individual batch of gasoline
produced at the refinery or
imported.
n = Total number of batches of gasoline
produced at the refinery or
imported during the applicable
annual averaging period.
Vi = Volume of gasoline in batch i
(gallons).
Bi = Benzene concentration of batch i
(volume percent benzene), per
§ 80.46(e).
(b) All input batch benzene
concentration values used in paragraph
(a) of this section shall be expressed to
two decimal places.
(c) Annual average benzene
concentration values calculated under
paragraph (a) of this section shall be
expressed to two decimal places using
conventional rounding methodology.
(d) A refiner or importer may include
the volume of oxygenate added
downstream from the refinery or import
facility in the calculation specified in
paragraph (a) of this section, provided
the following requirements are met:
(1) For oxygenate added to
conventional gasoline, the refiner or
importer must comply with the
requirements of § 80.101(d)(4)(ii) and
(g)(3).
(2) For oxygenate added to RBOB, the
refiner or importer must comply with
the requirements of § 80.69(a).
(e) Refiners and importers must
exclude from the calculation specified
in paragraph (a) of this section all of the
following:
(1) Gasoline that was not produced at
the refinery or imported by the
importer.
(2) Except as provided in paragraph
(c) of this section, any blendstocks or
unfinished gasoline transferred to
others.
(3) Gasoline that has been included in
the compliance calculations for another
refinery or importer.
(4) Gasoline exempted from the
standards under § 80.1235.
§ 80.1240 How is a refinery’s or importer’s
compliance with the gasoline benzene
requirements of this subpart determined?
(a)(1) The compliance benzene value
for a refinery or importer is:
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§ 80.1270 Who may generate benzene
credits under the ABT program?
(a) Early credits. (1) Early credits may
be generated under § 80.1275 by a
refiner for a refinery with an approved
benzene baseline under § 80.1285.
(2) Early credits may be generated
under § 80.1275 only by refiners that
produce gasoline by processing crude
oil through refinery processing units.
(3)(i) A refinery that was shut down
during the entire 2004–2005 benzene
baseline period is not eligible to
generate early credits under § 80.1275.
(ii) A refinery not in full production,
excluding normal refinery downtime, or
not showing consistent or regular
gasoline production activity during
2004–2005 may be eligible to generate
early benzene credits under § 80.1275
upon petition to and approval by EPA,
under § 80.1285.
(b) Standard Credits. (1) Standard
credits may be generated under
§ 80.1290 by refineries and importers for
gasoline produced or imported for use
in the U.S., excluding gasoline exempt
from the benzene standard under the
provisions of § 80.1235.
(2) Oxygenate blenders, butane
blenders, and transmix producers are
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Where:
Bavg = Annual average benzene
concentration (volume percent
benzene) of gasoline produced at
the refinery, per § 80.1238.
BBase = Baseline benzene concentration
(volume percent benzene) of the
refinery, per § 80.1280(b).
(2) Calculate the number of early
credits generated by the refinery for the
averaging period as follows:
BBase − Bavg
EC y =
× Ve
100
Where:
ECy = Early credits generated in year y
(gallons benzene).
Bavg = Annual average benzene
concentration (volume percent
benzene) of gasoline produced at
the refinery, per § 80.1238 that
satisfies the condition of paragraph
(d)(1) of this section.
Ve = Total volume of gasoline (gallons)
produced during the annual
averaging period at the refinery.
(e) All input benzene concentration
values used in paragraph (d) of this
section shall be expressed to two
decimal places.
(f) Early benzene credits calculated
under paragraph (d) of this section shall
be expressed to the nearest gallon using
conventional rounding methodology.
(g)(1) Early benzene credits shall be
calculated separately for each refinery.
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§ 80.1280 How are refinery benzene
baselines calculated?
(a) A refinery’s benzene baseline is
based on the refinery’s 2004–2005
average gasoline benzene concentration,
calculated according to the following
equation:
n
∑(V × B )
i
BBase =
i
i =1
n
∑V
i
i =1
Where:
BBase = Benzene baseline concentration
(volume percent benzene).
i = Individual batch of gasoline
produced at the refinery from
January 1, 2004 through December
31, 2005.
n = Total number of batches of gasoline
produced at the refinery from
January 1, 2004 through December
31, 2005 (or the total number of
batches of gasoline pursuant to
§ 80.1285(d)).
Vi = Volume of gasoline in batch i
(gallons).
Bi = Benzene content of batch i (volume
percent benzene).
(b) All input batch benzene
concentration values used in paragraph
(a) of this section shall be expressed to
two decimal places.
(c) Baseline benzene concentration
values calculated under paragraph (a) of
this section shall be expressed to two
decimal places using conventional
rounding methodology.
(d) Any refiner that, under § 80.69 or
§ 80.101(d)(4), included oxygenate
blended downstream in compliance
calculations for RFG or conventional
gasoline for calendar years 2004 or 2005
for a refinery must include the volume
and benzene concentration of this
oxygenate in the baseline calculations
for gasoline benzene content for that
refinery under paragraph (a) of this
section.
§ 80.1285 How does a refiner apply for a
benzene baseline?
(a) A refiner must submit an
application to EPA which includes the
information specified in paragraph (c) of
this section at least 60 days before the
refinery plans to begin generating early
credits.
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Averaging, Banking and Trading (ABT)
Program
(a) Early benzene credits may be
generated only if a refinery’s annual
average gasoline benzene concentration
is at least 10% lower than the refinery’s
approved baseline benzene
concentration per § 80.1280.
(b) [Reserved]
(c) The early credit annual averaging
periods are as follows:
(1) For 2007, the seven-month period
from June 1, 2007, through December
31, 2007, inclusive.
(2) For 2008, 2009 and 2010, the 12month calendar year.
(3) For 2011, 2012, 2013, and 2014,
which apply only to approved small
refiners per § 80.1340, the 12-month
calendar year.
(d) The number of early benzene
credits shall be calculated annually for
each applicable averaging period as
follows:
(1) Proceed to paragraph (d)(2) of this
section under the following condition.
Bavg ≤ BBase × 0.90
EP29MR06.011
D y −1
0.62
= Vy ×
− CBVy
100
§ 80.1275 How are early benzene credits
generated?
(2) Refiners shall not move gasoline or
gasoline blending stocks from one
refinery to another for the purpose of
generating early credits.
(h) An importer may not generate
early credits.
(i) A foreign refiner with an approved
baseline may generate early credits
subject to the provisions of § 80.1420.
EP29MR06.010
Where:
CBVy = Compliance benzene value
(gallons benzene) for year y.
Vy = Gasoline volume produced or
imported in year y (gallons).
Bavg = Annual average benzene
concentration (volume percent
benzene), per § 80.1238.
Dy-1 = Benzene deficit from the previous
reporting period, per § 80.1230(b)
(gallons benzene).
BC = Banked benzene credits used to
show compliance (gallons benzene).
RC = Benzene credits received by the
refinery or importer, per
§ 80.1295(c), used to show
compliance (gallons benzene).
(2) If CBVy ≤ Vy x (0.62)/100, then
compliance is achieved for calendar
year y.
(b)(1) A deficit is created when CBVy
> Vy x (0.62)/100.
(2) The deficit value to be included in
the following year’s compliance
calculation per paragraph (a) of this
section, is calculated as follows:
not eligible to generate standard credits
under § 80.1290.
EP29MR06.009
Bavg
CBVy = Vy ×
+ D y −1 − BC − RC
100
Federal Register / Vol. 71, No. 60 / Wednesday, March 29, 2006 / Proposed Rules
(b) The benzene baseline application
shall be sent to: U.S. EPA, Attn: Early
Gasoline Benzene Credits (6406J), 1200
Pennsylvania Ave., NW., Washington,
DC 20460. For commercial delivery:
U.S. EPA Attn: Early Gasoline Benzene
Credits (6406J), 501 3rd Street, NW.,
Washington, DC 20001.
(c) A benzene baseline application
must be submitted for each refinery that
plans to generate early credits under
§ 80.1275 and must include the
following information:
(1) A listing of the names and
addresses of all refineries owned by the
company.
(2) The benzene baseline for gasoline
produced in 2004–2005 at the refinery,
calculated in accordance with
§ 80.1280(b).
(3) Copies of the annual reports
required under § 80.75 for RFG and
§ 80.105 for conventional gasoline.
(4) A letter signed by the president,
chief operating officer, or chief
executive officer, of the company, or
his/her designee, stating that the
information contained in the benzene
baseline determination is true to the
best of his/her knowledge.
(5) Name, address, phone number,
facsimile number and e-mail address of
a corporate contact person.
(d) A refiner, for a refinery that
qualifies for generating early credits
under § 80.1270(a)(3)(ii) may submit to
EPA a benzene baseline application per
the requirements of this section. The
refiner must also submit information
regarding the nature and cause of the
inconsistent production, how it affects
the baseline and benzene concentration,
and whether an alternative calculation
to the calculation specified in § 80.1280
produces a more representative benzene
baseline value. EPA, upon consideration
of the submitted information, may
approve a benzene baseline for such a
refinery.
(e) Within 60 days of receipt of an
application under this section, except
for applications submitted in
accordance with paragraph (d) of this
section, EPA will notify the refiner of
approval of the refinery’s baseline or
any deficiencies in the application.
(f) If at any time the baseline
submitted in accordance with the
requirements of this section is
determined to be incorrect, EPA will
notify the refiner of the corrected
baseline.
§ 80.1290 How are benzene credits
generated in 2011 and beyond?
(a) Gasoline benzene standard credits
may be generated by the following
parties during any applicable averaging
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period specified in paragraph (b) of this
section:
(1) A refiner, at any of its refineries
that produce gasoline for use in the U.S.
(excluding gasoline under § 80.1235 that
is exempt from the requirements of this
subpart). Credits are generated
separately by each refinery;
(2) Importers, for all of their imported
gasoline (excluding gasoline under
§ 80.1235 that is exempt from the
requirements of this subpart);
(b) The standard credit averaging
periods are the calendar years beginning
with 2011, or beginning with 2015 for
approved small refiners.
(c) [Reserved]
(d)(1) The number of standard credits
generated by a refinery or importer shall
be calculated annually according to the
following equation:
0.62 − Bavg
SC y =
× Vy
100
Where:
SCy = Standard credits generated in year
y (gallons benzene).
Bavg = Annual average benzene
concentration for year y (volume
percent benzene), per § 80.1238.
Vy = Total volume of gasoline produced
or imported in year y (gallons).
(2) No credits shall be generated
unless the value SCy is positive.
(e) All input benzene concentration
values used in paragraph (d) of this
section shall be expressed to two
decimal places.
(f) Standard benzene credits
calculated under paragraph (d) of this
section shall be expressed to the nearest
gallon using conventional rounding
methodology.
(g) Foreign refiners may not generate
credits under this section.
§ 80.1295 How are gasoline benzene
credits used?
(a) Credit use. (1) Gasoline benzene
credits generated under §§ 80.1275 and
80.1290 may be used to comply with the
gasoline benzene content requirement of
§ 80.1230 provided that:
(i) The gasoline benzene credits were
generated and reported according to the
requirements of this subpart; and
(ii) The conditions of this section
§ 80.1295 are met.
(2) Gasoline benzene credits generated
under §§ 80.1275 and 80.1290 may be
used by a refiner or importer to comply
with the gasoline benzene content
standard of § 80.1230, may be banked by
a refiner or importer for future use or
transfer, may be transferred to another
refinery or importer within a company
(intracompany), or may be transferred to
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another refinery or importer outside of
the company.
(b) Credit banking. Gasoline benzene
credits generated by a refinery or
importer may be banked for use in a
later compliance period, or may be
transferred to another refiner, refinery,
or importer for use as provided in
paragraph (c) of this section.
(c) Credit transfers. (1) Gasoline
benzene credits obtained from another
refinery or importer may be used to
comply with the gasoline benzene
content requirement of § 80.1230
provided the following conditions are
met:
(i) The credits are generated and
reported according to the requirements
of this subpart, and the transferred
credit has not expired, per paragraph (d)
of this section.
(ii) Any credit transfer takes place no
later than the last day of February
following the calendar year averaging
period when the credits are used.
(iii) The credit has not been
transferred more than twice. The first
transfer by the refinery or importer that
generated the credit may only be made
to a refiner or importer that intends to
use the credit; if the transferee cannot
use the credit, it may make the second,
and final, transfer only to a refinery or
importer that intends to use or terminate
the credit. In no case may a credit be
transferred more than twice before being
used or terminated.
(iv) The credit transferor has applied
any gasoline benzene credits necessary
to meet its own annual compliance
requirements (and any deficit carryforward, if applicable) before
transferring any gasoline benzene
credits to any other refiner or importer.
(v) The credit transferor would not
create a deficit as a result of a credit
transfer.
(vi) The transferor supplies to the
transferee records indicating the year
the gasoline benzene credits were
generated, the identity of the refiner
(and refinery) or importer that generated
the gasoline benzene credits and the
identity of the transferring entity if not
the same entity that generated the
gasoline benzene credits.
(2) In the case of gasoline benzene
credits that have been calculated or
created improperly, or have otherwise
been determined to be invalid, the
following provisions apply:
(i) Invalid gasoline benzene credits
cannot be used to achieve compliance
with the gasoline benzene content
requirement of § 80.1230 regardless of
the transferee’s good faith belief that the
gasoline benzene credits were valid.
(ii) The refiner or importer that used
the gasoline benzene credits and any
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transferor of the gasoline benzene
credits must adjust their credit records,
reports, and compliance calculations as
necessary to reflect the proper gasoline
benzene credits.
(iii) Any properly created gasoline
benzene credits existing in the
transferor’s credit balance following the
corrections and adjustments specified in
paragraph (c)(2)(ii) of this section and
after the transferor applies gasoline
benzene credits as needed to meet its
own compliance requirements at the
end of the compliance period, must first
be applied to correct the invalid
transfers to the transferee, before the
transferor uses, trades or banks the
gasoline benzene credits.
(d) Credit life. (1) Early credits, per
§ 80.1275, may be used for compliance
purposes under § 80.1240 for any
calendar year averaging period prior to
the 2014 averaging period.
(2) Standard credits, per § 80.1290,
shall have a credit life of 5 calendar year
averaging periods after the year in
which they were generated. Example:
Standard credits generated during 2014
may be used to achieve compliance
under § 80.1240 for any calendar year
averaging period prior to the 2020
averaging period.
(3) Notwithstanding paragraphs (d)(1)
and (d)(2) of this section, credits traded
to or used by approved small refiners
per § 80.1340, have an additional credit
life of two calendar year averaging
periods.
(e) General limitations on credit use.
A refiner or importer possessing
gasoline benzene credits must use all
gasoline benzene credits in its
possession prior to applying the credit
deficit provisions of § 80.1230(b).
Hardship Provisions
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§ 80.1335 Can a refiner seek temporary
relief from the requirements of this
subpart?
(a) EPA may permit a refinery to have
an extended period of deficit carryforward, for the shortest period
practicable, per § 80.1230(b), if the
refiner demonstrates that:
(1) Unusual circumstances exist that
impose extreme hardship and
significantly affect the ability to comply
by the applicable date; and
(2) It has made best efforts to comply
with the requirements of this subpart,
including making all possible efforts to
obtain sufficient credits to meet the
standard.
(b) Applications must be submitted to
EPA by September 1, 2009.
(1) Approval of a hardship under this
section shall be in the form an extended
period of deficit carry-forward, per
§ 80.1230(b), for such period of time as
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EPA determines is appropriate, but shall
not extend beyond December 31, 2014.
(2) EPA reserves the right to deny
applications for appropriate reasons,
including unacceptable environmental
impact.
(c)(1) Applications must include a
plan demonstrating how the refiner will
comply with the requirements of this
subpart as expeditiously as possible.
The plan shall include a showing that
contracts are or will be in place for
engineering and construction of benzene
reduction technology, a plan for
applying for and obtaining any permits
necessary for construction, a description
of plans to obtain necessary capital, and
a detailed estimate of when the
requirements of this subpart will be met.
(2) Applications must include a
detailed description of the refinery
configuration and operations including,
at minimum, the following information:
(i) The refinery’s total reformer unit
throughput capacity;
(ii) The refinery’s total crude capacity;
(iii) Total crude capacity of any other
refineries owned by the same entity;
(iv) Total volume of gasoline
production at the refinery;
(v) Total volume of other refinery
products; and
(vi) Geographic location(s) where the
refinery’s gasoline will be sold.
(3) Applications must include, at a
minimum, the following information:
(i) Detailed descriptions of efforts to
obtain capital for refinery investments;
(ii) Detailed descriptions of efforts to
obtain credits;
(iii) Bond rating of entity that owns
the refinery; and
(iv) Estimated capital investment
needed to comply with the requirements
of this subpart
(4) Applicants must also provide any
other relevant information requested by
EPA.
(d) EPA may impose any reasonable
conditions on waivers granted under
this section, including the condition
that if more credits are available than
was anticipated at the time of the
hardship approval, the extended period
of deficit carry-forward may be
shortened.
§ 80.1336 What if a refiner or importer
cannot produce gasoline conforming to the
requirements of this subpart?
In extreme and unusual
circumstances (e.g., natural disaster or
Act of God) which are clearly outside
the control of the refiner or importer
and which could not have been avoided
by the exercise of prudence, diligence,
and due care, EPA may permit a refinery
or importer to extend the deadline for
meeting the deficit carry-forward
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requirements under § 80.1230(b) for a
brief period (e.g., where appropriate,
EPA may allow one or more additional
weeks after the last day of February to
purchase credits), provided the refinery
or importer meets all the criteria,
requirements and conditions contained
in § 80.73(a) through (e).
Small Refiner Provisions
§ 80.1338 What is the definition of a small
refiner for the purpose of the gasoline
benzene requirements of this subpart?
(a) A small refiner is defined as any
person, as defined by 42 U.S.C. 7602(e),
that—
(1) Produced gasoline at a refinery by
processing crude oil through refinery
processing units from January 1, 2005,
through December 31, 2005; and
(2) Employed an average of no more
than 1,500 people, based on the average
number of employees for all pay periods
from January 1, 2005 through December
31, 2005; and
(3) Had a corporate average crude oil
capacity less than or equal to 155,000
barrels per calendar day (bpcd) for 2005;
or
(4) Has been approved by EPA as a
small refiner under § 80.1340.
(b) For the purpose of determining the
number of employees and the crude oil
capacity under paragraph (a) of this
section, the following determinations
shall be observed:
(1) The refiner shall include the
employees and crude oil capacity of any
subsidiary companies, any parent
company and subsidiaries of the parent
company in which the parent has a
controlling interest, and any joint
venture partners.
(2) For any refiner owned by a
governmental entity, the number of
employees and total crude oil capacity
as specified in paragraph (a) of this
section shall include all employees and
crude oil production of the government
to which the governmental entity is a
part.
(3) Any refiner owned and controlled
by an Alaska Regional or Village
Corporation organized pursuant to the
Alaska Native Claims Settlement Act (43
U.S.C. 1601) is not considered an
affiliate of such entity, or with other
concerns owned by such entity, solely
because of their common ownership.
(c) Notwithstanding the provisions of
paragraph (a) of this section, a refiner
that reactivates a refinery, which it
previously operated, and that was shut
down or non-operational for the entire
period between January 1, 2005, and
December 31, 2005, may apply for small
refiner status in accordance with the
provisions of § 80.1340.
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§ 80.1339 Who is not eligible for the
provisions for small refiners?
(a) The following are not eligible for
the hardship provisions for small
refiners:
(1) Refiners with refineries built after
December 31, 2005;
(2) Refiners that exceed the employee
or crude oil capacity criteria under
§ 80.1338 but that meet these criteria
after December 31, 2005, regardless of
whether the reduction in employees or
crude capacity is due to operational
changes at the refinery or a company
sale or reorganization.
(3) Importers.
(4) Refiners that produce gasoline
other than by processing crude oil
through refinery processing units.
(b)(1)(i) Refiners that qualify as small
under § 80.1338 and subsequently cease
production of gasoline from processing
crude oil through refinery processing
units, employ more than 1,500 people or
exceed the 155,000 bpcd crude oil
capacity limit after December 31, 2005,
as a result of merger with or acquisition
of or by another entity, are disqualified
as small refiners, except this shall not
apply in the case of a merger between
two previously approved small refiners.
If disqualification occurs, the refiner
shall notify EPA in writing no later than
20 days following this disqualifying
event.
(ii) Except as provided under
paragraph (b)(1)(iii) of this section, any
refiner whose status changes under this
paragraph (b) shall meet the applicable
standards of § 80.1230 within a period
of up to 30 months of the disqualifying
event for all of its refineries. However,
such period shall not extend beyond
December 31, 2014.
(iii) A refiner may apply to EPA for
an additional six months to comply
with the standards of § 80.1230 if more
than 30 months will be required for the
necessary engineering, permitting,
construction, and start-up work to be
completed. Such applications must
include detailed technical information
supporting the need for additional time.
EPA will base its decision to approve
additional time on the information
provided by the refiner and on other
relevant information. In no case will
EPA extend the compliance date beyond
December 31, 2014.
(iv) During the period of time of up to
30 months provided under paragraph
(b)(1)(ii) of this section, and any
extension provided under paragraph
(b)(1)(iii) of this section, the refiner may
not generate gasoline benzene credits
under § 80.1275 or § 80.1290.
(2) An approved small refiner per
§ 80.1340 may elect to meet the
requirements of § 80.1230 applicable to
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non-small refiners by notifying EPA in
writing no later than November 15 prior
to the year that the change will occur.
Any refiner whose status changes under
this paragraph (b)(2) shall meet the
requirements for non-small refiners
under § 80.1230 beginning with the first
averaging period subsequent to the
status change.
§ 80.1340 How does a refiner obtain
approval as a small refiner?
(a) Applications for small refiner
status must be submitted to EPA by
December 31, 2007.
(b) Applications for small refiner
status must be sent to: U.S. EPA, Attn:
MSAT2 Benzene (6406J), 1200
Pennsylvania Ave., NW., Washington,
DC 20460. For commercial delivery:
U.S. EPA Attn: MSAT2 Benzene (6406J),
501 3rd Street, NW., Washington, DC
20001.
(c) The small refiner status
application must contain the following
information for the company seeking
small refiner status, and for all
subsidiary companies, all parent
companies, all subsidiaries of the parent
companies, and all joint venture
partners:
(1) Employees. (i) A listing of the
names and addresses of each location
where any employee worked during the
12 months preceding January 1, 2006;
(ii) The average number of employees
at each location based upon the number
of employees for each pay period for the
12 months preceding January 1, 2006;
and
(iii) The type of business activities
carried out at each location.
(iv) In the case of a refiner that
reactivates a refinery that it previously
owned and operated and that was shut
down or non-operational between
January 1, 2005, and January 1, 2006,
include the following:
(A) A listing of the name and address
of each location where any employee of
the refiner worked since the refiner
acquired or reactivated the refinery;
(B) The average number of employees
at any such reactivated refinery during
each calendar year since the refiner
reactivated the refinery; and
(C) The type of business activities
carried out at each location.
(vi) For joint ventures, the total
number of employees includes the
combined employee count of all
corporate entities in the venture.
(vii) For government-owned refiners,
the total employee count includes all
government employees.
(2) Crude oil capacity. (i) The total
corporate crude oil capacity of each
refinery as reported to the Energy
Information Administration (EIA) of the
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U.S. Department of Energy (DOE), for
the period January 1, 2005, through
December 31, 2005.
(ii) The information submitted to EIA
is presumed to be correct. In cases
where a company disagrees with this
information, the company may petition
EPA with appropriate data to correct the
record when the company submits its
application for small refiner status.
(3) The type of business activity
carried out at each location.
(4) For each refinery, an indication of
the small refiner option(s) intended to
be utilized at the refinery.
(5) A letter signed by the president,
chief operating or chief executive officer
of the company, or his/her designee,
stating that the information contained in
the application is true to the best of his/
her knowledge, and that the company
owned the refinery as of January 1,
2006.
(6) Name, address, phone number,
facsimile number, and E-mail address of
a corporate contact person.
(d) Approval of a small refiner status
application will be based on all
information submitted under paragraph
(c) of this section and any other relevant
information.
(e) EPA will notify a refiner of
approval or disapproval of small refiner
status by letter.
(1) If approved, all refineries of the
refiner may defer meeting the standard
specified in § 80.1230 until the annual
averaging period beginning January 1,
2015.
(2) If disapproved, all refineries of the
refiner must meet the standard specified
in § 80.1230 beginning with the annual
averaging period beginning January 1,
2011.
(f) If EPA finds that a refiner provided
false or inaccurate information on its
application for small refiner status,
upon notice from EPA, the refiner’s
small refiner status will be void ab
initio.
(g) Prior to January 1, 2014, and upon
notification to EPA, an approved small
refiner per this section may withdraw
its status as a small refiner. Effective on
January 1 of the year following such
notification, the small refiner will
become subject to the standards at
§ 80.1230.
§ 80.1342 What compliance options are
available to small refiners under this
subpart?
(a) A refiner that has been approved
as a small refiner under § 80.1340 may—
(1) Defer meeting the standard
specified in section § 80.1230 until the
annual averaging period January 1,
2015; or
(2) Meet the standard specified in
§ 80.1230 beginning January 1 of any of
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the following annual averaging periods:
2007, 2008, 2009, 2010, 2011, 2012,
2013, and 2014.
(b) The provisions of paragraph (a) of
this section shall apply separately for
each of an approved small refiner’s
refineries.
§ 80.1344 What provisions are available to
a large refiner that acquires one or more of
a small refiner’s refineries?
(a) In the case of a refiner without
approved small refiner status that
acquires a refinery from an approved
small refiner per § 80.1340, the small
refiner provisions of the gasoline
benzene program of this subpart may
continue to apply to the acquired
refinery for a period of up to 30 months
from the date of acquisition of the
refinery. In no case shall this period
extend beyond December 31, 2014.
(b) A refiner may apply to EPA for up
to an additional six months to comply
with the standards of § 80.1230 for the
acquired refinery if more than 30
months would be required for the
necessary engineering, permitting,
construction, and start-up work to be
completed. Such applications must
include detailed technical information
supporting the need for additional time.
EPA will base a decision to approve
additional time on information provided
by the refiner and on other relevant
information. In no case shall this period
extend beyond December 31, 2014.
(c) A refiner that acquires a refinery
from an approved small refiner per
§ 80.1340 shall notify EPA in writing no
later than 20 days following the
acquisition.
Sampling, Testing and Retention
Requirements
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§ 80.1347 What are the sampling and
testing requirements for refiners and
importers?
(a) Sample and test each batch of
gasoline. Refiners and importers shall
collect a representative sample from
each batch of gasoline produced or
imported. Each sample shall be tested in
accordance the methodology specified
at § 80.46(e) to determine its benzene
concentration for compliance with the
requirements of this subpart.
(b) Batch numbering. The batch
numbering convention of § 80.365(b)(2)
shall apply to batches of conventional
gasoline.
(c) The requirements of this section
apply to any refiner or importer subject
to the requirements of this subpart,
including those generating early credits
per § 80.1275, all non-small refiners and
importers beginning January 1, 2011,
and small refiners beginning January 1,
2015.
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§ 80.1348 What gasoline sample retention
requirements apply to refiners and
importers?
The gasoline sample retention
requirements specified in subpart H of
this part for the gasoline sulfur
provisions apply for the purpose of
complying with the requirements of this
subpart, except that in addition to
including the sulfur test result as
provided by § 80.335(a)(4)(ii), the
refiner, importer, or independent
laboratory shall also include with the
retained sample the test result for
benzene as conducted pursuant to
§ 80.46(e).
Recordkeeping and Reporting
Requirements
§ 80.1350
What records must be kept?
(a) General requirements. The
recordkeeping requirements specified in
§ 80.74 and § 80.104, as applicable,
apply for the purpose of complying with
the requirements of this subpart,
however, duplicate records are not
required.
(b) Additional records that refiners
and importers shall keep. Beginning
January 1, 2007, any refiner for each of
its refineries, and any importer for the
gasoline it imports, shall keep records
that include the following information
(including any supporting calculations
as applicable):
(1) Its compliance benzene value per
§ 80.1240, and the calculations used to
obtain that value.
(2) Its benzene baseline value, per
§ 80.1280, if the refinery or importer
submitted a benzene baseline
application to EPA per § 80.1285;
(3) The number of early benzene
credits generated under § 80.1275,
separately by year of generation;
(4) The number of early benzene
credits obtained, separately by
generating refinery and year of
generation;
(5) The number of valid credits in
possession of the refinery or importer at
the beginning of each averaging period,
separately by generating facility and
year of generation;
(6) The number of standard credits
generated by the refinery or importer
under § 80.1290, separately by transferor
(if applicable), and by year of
generation;
(7) The number of credits used,
separately by generating facility and
year of generation;
(8) If any credits were obtained from,
or transferred to, other parties, for each
other party, its name, its EPA refinery or
importer registration number, and the
number of credits obtained from, or
transferred to, the other party;
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(9) The number of credits that expired
at the end of the averaging period,
separately by generating facility and
year of generation;
(10) The number of credits that will
be carried over into the subsequent
averaging period, separately by
generating facility and year of
generation;
(11) Contracts or other commercial
documents that establish each transfer
of credits from the transferor to the
transferee; and
(12) A copy of all reports submitted to
EPA under §§ 80.1352 and 80.1354,
however, duplicate records are not
required.
(c) Length of time records shall be
kept. The records required by this
section shall be kept for five years from
the end of the annual averaging period
during which they were created, or
seven years for records pertaining to
credits traded to a small refiner in
accordance with § 80.1295(d)(3), except
where longer record retention is
required elsewhere in this subpart.
(d) Make records available to EPA. On
request by EPA, the records specified in
this section shall be provided to the
Administrator. For records that are
electronically generated or maintained,
the equipment and software necessary
to read the records shall be made
available, or upon approval by EPA,
electronic records shall be converted to
paper documents which shall be
provided to the Administrator.
§ 80.1352 What are the pre-compliance
reporting requirements for the gasoline
benzene program?
(a) Except as provided in paragraph
(c) of this section, a refiner for each of
its refineries shall submit the following
information to EPA beginning June 1,
2008, and annually thereafter through
June 1, 2011, or through June 1, 2015,
for small refiners:
(1) Changes to the information
submitted in the company’s registration;
(2) Changes to the information
submitted for any refinery or import
facility registration;
(3) Gasoline production. (i) An
estimate of the average daily volume (in
gallons) of gasoline produced at each
refinery. This estimate shall include
RFG, RBOB, conventional gasoline and
conventional gasoline blendstock that
becomes finished gasoline solely upon
the addition of oxygenate but shall
exclude gasoline exempted pursuant to
§ 80.1235;
(ii) These volume estimates must be
provided for the periods of June 1, 2007,
through December 31, 2007, and
calendar years 2008, 2009 and 2010.
(4) Benzene concentration. An
estimate of the average gasoline benzene
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concentration corresponding to the time
periods specified in paragraph (a)(3) of
this section.
(5) ABT Participation. If the refinery
is expecting to participate in the credit
trading program under § 80.1275 and/or
§ 80.1290, the actual or estimated, as
applicable, numbers of early credits and
standard credits expected to be
generated and/or used each year
through 2015.
(6) Information on any project
schedule by quarter of known or
projected completion date by the stage
of the project, for example, following
the five project phases described in
EPA’s June 2002 Highway Diesel
Progress Review report (EPA420–R–02–
016, https://www.epa.gov/otaq/regs/
hd2007/420r02016.pdf): Strategic
planning, Planning and front-end
engineering, Detailed engineering and
permitting, Procurement and
Construction, and Commissioning and
startup;
(7) Basic information regarding the
selected technology pathway for
compliance (e.g., precursor re-routing or
other technologies, revamp vs.
grassroots, etc.);
(8) Whether capital commitments
have been made or are projected to be
made.
(b) The pre-compliance reports due in
2008 and succeeding years must provide
an update of the progress in each of
these areas and actual values where
available.
(c) The pre-compliance reporting
requirements of this section do not
apply to refineries exempted under the
provisions of § 80.1230(c)(1).
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§ 80.1354 What are the reporting
requirements for the gasoline benzene
program?
(a) Beginning with the 2011 annual
averaging period, or the 2015 annual
averaging period for small refiners, and
continuing for each averaging period
thereafter, every refiner, for each of its
refineries, and every importer shall
submit to EPA the information required
in this section, and such other
information as EPA may require.
(b) Beginning with the 2007 annual
averaging period for refiners generating
early credits pursuant to § 80.1275 or
§ 80.1290(b) for approved small refiners,
every refiner for each of its refineries
shall submit to EPA the information
required in this section, and such other
information as EPA may require.
(c) Refiner and importer annual
reports. Any refiner, for each of its
refineries, and any importer for the
gasoline it imports, shall submit a
Gasoline Benzene Report containing the
following information:
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(1) Benzene volume percent and
volume of any RFG, RBOB, and
conventional gasoline, separately by
batch, produced by the refinery or
imported, and the sum of the volumes
and the volume-weighted benzene
concentration, in volume percent;
(2) The annual average benzene
concentration, per § 80.1240, § 80.1275
or § 80.1290, as applicable;
(3) Any benzene deficit from the
previous reporting period, per
§ 80.1230(b);
(4) The number of banked benzene
credits from the previous reporting
period;
(5) The number of benzene credits
generated under § 80.1275, if applicable;
(6) The number of benzene credits
generated under § 80.1290, if applicable;
(7) The number of benzene credits
transferred to the refinery or importer,
per § 80.1295(c), and the cost of the
credits, if applicable;
(8) The number of benzene credits
transferred from the refinery or
importer, per § 80.1295(c), and the price
of the credits, if applicable;
(9) The number of benzene credits
terminated or expired;
(10) The compliance benzene value
specified in § 80.1240;
(11) The number of banked benzene
credits;
(12) Projected credit generation
through compliance year 2015; and
(13) Projected credit use through
compliance year 2015.
(d) EPA may require submission of
additional information to verify
compliance with the requirements of
this subpart.
(e) The report required by paragraph
(a) of this section shall be:
(1) Submitted on forms and following
procedures specified by the
Administrator of EPA;
(2) Submitted to EPA by the last day
of February each year for the prior
calendar year averaging period; and
(3) Signed and certified as correct by
the owner or a responsible corporate
officer of the refiner or importer.
Attest Engagements
§ 80.1375 What are the attest engagement
requirements for gasoline benzene
compliance?
In addition to the requirements for
attest engagements that apply to refiners
and importers under §§ 80.125 through
80.130, 80.410, and 80.1030, the attest
engagements for refiners and importers
must include the following procedures
and requirements each year.
(a) EPA early credit generation
baseline years’ reports.
(1) Obtain and read a copy of the
refinery’s or importer’s annual reports
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and batch reports filed with EPA for
2004 and 2005 which contain gasoline
benzene and gasoline volume
information.
(2) Agree the yearly volumes of
gasoline and benzene concentration, in
volume percent and benzene gallons,
reported to EPA in the reports specified
in paragraph (a)(1) of this section with
the inventory reconciliation analysis
under § 80.128.
(3) Verify that the information in the
refinery’s or importer’s batch reports
filed with EPA under §§ 80.75 and
80.105, and any laboratory test results,
agree with the information contained in
the reports specified in paragraph (a)(1)
of this section.
(4) Calculate the average benzene
concentration for all of the refinery’s or
importer’s gasoline volume over 2004
and 2005 and verify that those values
agree with the values reported to EPA
per § 80.1285.
(b) Baseline for early credit
generation. For the first attest reporting
period following approval of a benzene
baseline:
(1) Obtain the EPA benzene baseline
approval letter for the refinery to
determine the refinery’s applicable
benzene baseline under § 80.1285.
(2) Obtain a written representation
from the company representative stating
the benzene value used as the refinery’s
baseline and agree that number to
paragraph (b)(1) of this section and to
the reports to EPA.
(c) Early credit generation. The
following procedures shall be
completed for a refinery or importer that
generates early benzene credits per
§ 80.1275:
(1) Obtain the baseline benzene
concentration and gasoline volume from
paragraph (a)(4) of this section.
(2) Obtain the annual benzene report
per § 80.1354.
(3) If the benzene value under
paragraph (c)(2) of this section is at least
10 percent less than value in paragraph
(c)(1) of this section, compute and
report as a finding the difference
according to § 80.1275.
(4) Compute and report as a finding
the total number of benzene credits
generated by multiplying the value
calculated in paragraph (c)(3) of this
section by the volume of gasoline listed
in the report specified in paragraph
(c)(2) of this section, and agree this
number with the number reported to
EPA.
(d) Standard credit generation. The
following procedures shall be
completed for a refinery or importer that
generates benzene credits per § 80.1290:
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(1) Obtain the annual average benzene
value from the annual benzene report
per § 80.1285.
(2) If the annual average benzene
value under paragraph (d)(1) of this
section is less than 0.62 percent by
volume, compute and report as a finding
the difference according to § 80.1290.
(3) Compute and report as a finding
the total number of benzene credits
generated by multiplying the value
calculated in paragraph (d)(2) of this
section by the volume of gasoline listed
in the report specified in paragraph
(d)(1) of this section, and agree this
number with the number reported to
EPA.
(e) Credits required. The following
attest procedures shall be completed for
refineries and importers:
(1) Obtain the annual average benzene
concentration and volume from the
annual benzene report per § 80.1285.
(2) If the value in paragraph (e)(1) of
this section is greater than 0.62 percent
by volume, compute and report as a
finding the difference between 0.62
percent by volume and the value in
paragraph (e)(1) of this section.
(3) Compute and report as a finding
the total benzene credits required by
multiplying the value in paragraph
(e)(2) of this section times the volume of
gasoline in paragraph (e)(1) of this
section, and agree with the report to
EPA.
(4) Obtain the refiner’s or importer’s
representation as to the portion of the
deficit under paragraph (e)(3) of this
section that was resolved with credits,
or that was carried forward as a deficit
under § 80.1230(b), and agree with the
report to EPA.
(f) Credit purchases and sales. The
following attest procedures shall be
completed for a refinery or importer that
is a transferor or transferee of credits
during an averaging period:
(1) Obtain contracts or other
documents for all credits transferred to
another refinery or importer during the
year being reviewed; compute and
report as a finding the number and year
of creation of credits represented in
these documents as being transferred;
and agree with the report to EPA.
(2) Obtain contracts or other
documents for all credits received
during the year being reviewed;
compute and report as a finding the
number and year of creation of credits
represented in these documents as being
received; and agree with the report to
EPA.
(g) Credit reconciliation. The
following attest procedures shall be
completed each year credits were in the
refiner’s or importer’s possession at any
time during the year:
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(1) Obtain the credits remaining or the
credit deficit from the previous year
from the refiner’s or importer’s report to
EPA for the previous year.
(2) Compute and report as a finding
the net credits remaining at the
conclusion of the year being reviewed
by totaling:
(i) Credits remaining from the
previous year; plus
(ii) Credits generated under
paragraphs (c) and (d) of this section;
plus
(iii) Credits purchased under
paragraph (f) of this section; minus
(iv) Credits sold under paragraph (f) of
this section; minus
(v) Credits used under paragraphs (e)
of this section; minus
(vi) Credits expired; minus
(vii) Credit deficit from the previous
year.
(3) Agree the credits remaining or the
credit deficit at the conclusion of the
year being reviewed with the report to
EPA.
(4) If the refinery or importer had a
credit deficit for both the previous year
and the year being reviewed, report this
fact as a finding.
Violations and Penalties
§ 80.1400 What acts are prohibited under
the gasoline benzene program?
No person shall:
(a) Averaging violation. Produce or
import gasoline subject to this subpart
that does not comply with the
applicable benzene average standard
requirement under § 80.1230.
(b) Causing an averaging violation.
Cause another person to commit an act
in violation of paragraph (a) of this
section.
(c) Fail to meet the recordkeeping and
reporting requirements, or any other
requirements of this subpart.
§ 80.1405 What evidence may be used to
determine compliance with the prohibitions
and requirements of this subpart and
liability for violations of this subpart?
(a) Compliance with the benzene
standard of this subpart shall be
determined based on the benzene
concentration of the gasoline, measured
using the methodologies specified in
§ 80.46(e). Any evidence or information,
including the exclusive use of such
evidence or information, may be used to
establish the benzene concentration of
the gasoline if the evidence or
information is relevant to whether the
benzene concentration of the gasoline
would have been in compliance with
the standard if the appropriate sampling
and testing methodologies had been
correctly performed. Such evidence may
be obtained from any source or location
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15947
and may include, but is not limited to,
test results using methods other than
those specified in § 80.46(e), business
records and commercial documents.
(b) Determinations of compliance
with the requirements of this subpart
other than the benzene standard, and
determinations of liability for any
violation of this subpart, may be based
on information from any source or
location. Such information may include,
but is not limited to, business records
and commercial documents.
§ 80.1410 Who is liable for violations
under the gasoline benzene program?
(a) Persons liable for violations of
prohibited acts.
(1) Averaging violation. Any refiner or
importer that violates § 80.1400(a) is
liable for a violation of § 80.1400(a).
(2) Causing an averaging violation.
Any person that causes another party to
violate § 80.1400(a) is liable for a
violation of § 80.1400(b).
(3) Parent corporation liability. Any
parent corporation is liable for any
violations of this subpart that are
committed by any of its wholly-owned
subsidiaries.
(4) Joint venture and joint owner
liability. Each partner to a joint venture,
or each owner of a facility owned by
two or more owners, is jointly and
severally liable for any violation of this
subpart that occurs at the joint venture
facility or facility that is owned by the
joint owners, or that is committed by the
joint venture operation or any of the
joint owners of the facility.
(b) Persons liable for failure to meet
other provisions of this subpart.
(1) Any person that fails to meet a
provision of this subpart not addressed
in paragraph (a) of this section is liable
for a violation of that provision.
(2) Any person that caused another
person to fail to meet a requirement of
this subpart not addressed in paragraph
(a) of this section, is liable for causing
a violation of that provision.
§ 80.1415 What penalties apply under the
gasoline benzene program?
(a) Any person liable for a violation
under § 80.1410 is subject to civil
penalties as specified in sections 205
and 211(d) of the Clean Air Act for
every day of each such violation and the
amount of economic benefit or savings
resulting from each violation.
(b) Any person liable under
§ 80.1400(a) for a violation of the
applicable benzene average standard or
causing another person to violate the
requirement during any averaging
period, is subject to a separate day of
violation for each and every day in the
averaging period. Any person liable
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under § 80.1410(b) for a failure to fulfill
any requirement of credit generation,
transfer, use, banking, or deficit carryforward correction is subject to a
separate violation for each and every
day in the averaging period in which
invalid credits are generated, banked,
transferred or used.
(c) Any person liable under
§ 80.1410(b) for failure to meet, or
causing a failure to meet, a provision of
this subpart is liable for a separate day
of violation for each and every day such
provision remains unfulfilled.
Foreign Refiners
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§ 80.1420 What are the additional
requirements under this subpart for
gasoline produced at foreign refineries?
(a) Definitions. (1) A foreign refinery
is a refinery that is located outside the
United States, the Commonwealth of
Puerto Rico, the Virgin Islands, Guam,
American Samoa, and the
Commonwealth of the Northern Mariana
Islands (collectively referred to in this
section as ‘‘the United States’’).
(2) A foreign refiner is a person that
meets the definition of refiner under
§ 80.2(i) for a foreign refinery.
(3) Benzene-FRGAS means gasoline
produced at a foreign refinery that has
been assigned an individual refinery
benzene baseline under § 80.1285, has
been approved as a small refiner under
§ 80.1340, or has been granted
temporary relief under § 80.1335, and
that is imported into the United States.
(4) Non-Benzene-FRGAS means
(i) Gasoline meeting any of the
conditions specified in paragraph (a)(3)
of this section that is not imported into
the United States.
(ii) Gasoline meeting any of the
conditions specified in paragraph (a)(3)
of this section during a year when the
foreign refiner has opted to not
participate in the Benzene-FRGAS
program under paragraph (c)(3) of this
section.
(iii) Gasoline produced at a foreign
refinery that has not been assigned an
individual refinery benzene baseline
under § 80.1285, or that has not been
approved as a small refiner under
§ 80.1340, or that has not been granted
temporary relief under § 80.1335.
(5) Certified Benzene-FRGAS means
Benzene-FRGAS the foreign refiner
intends to include in the foreign
refinery’s benzene compliance
calculations under § 80.1240 or credit
calculations under § 80.1275 and does
include in these calculations when
reported to EPA.
(7) Non-Certified Benzene-FRGAS
means Benzene-FRGAS that is not
Certified Benzene-FRGAS.
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(b) Baseline for early credits. For any
foreign refiner to obtain approval under
the benzene foreign refiner program of
this subpart for any refinery in order to
generate early credits under § 80.1275, it
must apply for approval under the
applicable provisions of this subpart.
(1) The refiner shall follow the
procedures, applicable to volume
baselines in §§ 80.91 through 80.93 to
establish the volume of gasoline that
was produced at the refinery and
imported into the United States during
the applicable years for purposes of
establishing a baseline under § 80.1280
for applicable fuels produced for use in
the United States.
(2) In making determinations for
foreign refinery baselines EPA will
consider all information supplied by a
foreign refiner, and in addition may rely
on any and all appropriate assumptions
necessary to make such determinations.
(3) Where a foreign refiner submits a
petition that is incomplete or
inadequate to establish an accurate
baseline, and the refiner fails to correct
this deficiency after a request for more
information, EPA will not assign an
individual refinery baseline.
(c) General requirements for BenzeneFRGAS foreign refiners. A foreign
refiner of a refinery that is approved
under the benzene foreign refiner
program of this subpart must designate
each batch of gasoline produced at the
foreign refinery that is exported to the
United States as either Certified
Benzene-FRGAS or as Non-Certified
Benzene-FRGAS, except as provided in
paragraph (c)(3) of this section.
(1) In the case of Certified BenzeneFRGAS, the foreign refiner must meet
all requirements that apply to refiners
under this subpart.
(2) In the case of Non-Certified
Benzene-FRGAS, the foreign refiner
shall meet all the following
requirements:
(i) The designation requirements in
this section;
(ii) The recordkeeping requirements
in this section and in § 80.1350;
(iii) The reporting requirements in
this section and in §§ 80.1352 and
80.1354;
(iv) The product transfer document
requirements in this section;
(v) The prohibitions in this section
and in § 80.1400; and
(vi) The independent audit
requirements in this section and in
§ 80.1375.
(3)(i) Any foreign refiner that
generates early benzene credits under
§ 80.1275 shall designate all BenzeneFRGAS as Certified Benzene-FRGAS for
any year that such credits are generated.
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(ii) Any foreign refiner that has been
approved to produce gasoline subject to
the benzene foreign refiner program for
a foreign refinery under this subpart
may elect to classify no gasoline
imported into the United States as
Benzene-FRGAS provided the foreign
refiner notifies EPA of the election no
later than November 1 preceding the
beginning of the next compliance
period.
(iii) An election under paragraph
(c)(3)(ii) of this section shall be for a 12
month compliance period and apply to
all gasoline that is produced by the
foreign refinery that is imported into the
United States, and shall remain in effect
for each succeeding year unless and
until the foreign refiner notifies EPA of
the termination of the election. The
change in election shall take effect at the
beginning of the next annual
compliance period.
(d) Designation, product transfer
documents, and foreign refiner
certification. (1) Any foreign refiner of a
foreign refinery that has been approved
by EPA to produce gasoline subject to
the benzene foreign refiner program
must designate each batch of BenzeneFRGAS as such at the time the gasoline
is produced, unless the refiner has
elected to classify no gasoline exported
to the United States as Benzene-FRGAS
under paragraph (c)(3) of this section.
(2) On each occasion when any
person transfers custody or title to any
Benzene-FRGAS prior to its being
imported into the United States, it must
include the following information as
part of the product transfer document
information:
(i) Designation of the gasoline as
Certified Benzene-FRGAS or as NonCertified Benzene-FRGAS; and
(ii) The name and EPA refinery
registration number of the refinery
where the Benzene-FRGAS was
produced.
(3) On each occasion when BenzeneFRGAS is loaded onto a vessel or other
transportation mode for transport to the
United States, the foreign refiner shall
prepare a certification for each batch of
the Benzene-FRGAS that meets the
following requirements.
(i) The certification shall include the
report of the independent third party
under paragraph (f) of this section, and
the following additional information:
(A) The name and EPA registration
number of the refinery that produced
the Benzene-FRGAS;
(B) The identification of the gasoline
as Certified Benzene-FRGAS or NonCertified Benzene-FRGAS;
(C) The volume of Benzene-FRGAS
being transported, in gallons;
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(D) In the case of Certified BenzeneFRGAS:
(1) The benzene content as
determined under paragraph (f) of this
section, and the applicable designations
stated in paragraph (d)(2)(i) of this
section; and
(2) A declaration that the BenzeneFRGAS is being included in the
applicable compliance calculations
required by EPA under this subpart.
(ii) The certification shall be made
part of the product transfer documents
for the Benzene-FRGAS.
(e) Transfers of Benzene-FRGAS to
non-United States markets. The foreign
refiner is responsible to ensure that all
gasoline classified as Benzene-FRGAS is
imported into the United States. A
foreign refiner may remove the BenzeneFRGAS classification, and the gasoline
need not be imported into the United
States, but only if:
(1) The foreign refiner excludes:
(i) The volume of gasoline from the
refinery’s compliance report under
§ 80.1354; and
(ii) In the case of Certified BenzeneFRGAS, the volume of the gasoline from
the compliance report under § 80.1354.
(2) The foreign refiner obtains
sufficient evidence in the form of
documentation that the gasoline was not
imported into the United States.
(f) Load port independent sampling,
testing and refinery identification. (1)
On each occasion that Benzene-FRGAS
is loaded onto a vessel for transport to
the United States a foreign refiner shall
have an independent third party:
(i) Inspect the vessel prior to loading
and determine the volume of any tank
bottoms;
(ii) Determine the volume of BenzeneFRGAS loaded onto the vessel
(exclusive of any tank bottoms before
loading);
(iii) Obtain the EPA-assigned
registration number of the foreign
refinery;
(iv) Determine the name and country
of registration of the vessel used to
transport the Benzene-FRGAS to the
United States; and
(v) Determine the date and time the
vessel departs the port serving the
foreign refinery.
(2) On each occasion that Certified
Benzene-FRGAS is loaded onto a vessel
for transport to the United States a
foreign refiner shall have an
independent third party:
(i) Collect a representative sample of
the Certified Benzene-FRGAS from each
vessel compartment subsequent to
loading on the vessel and prior to
departure of the vessel from the port
serving the foreign refinery;
(ii) Determine the benzene content
value for each compartment using the
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methodology as specified in § 80.46(e)
by one of the following:
(A) The third party analyzing each
sample; or
(B) The third party observing the
foreign refiner analyze the sample;
(iii) Review original documents that
reflect movement and storage of the
Certified Benzene-FRGAS from the
refinery to the load port, and from this
review determine:
(A) The refinery at which the
Benzene-FRGAS was produced; and
(B) That the Benzene-FRGAS
remained segregated from:
(1) Non-Benzene-FRGAS and NonCertified Benzene-FRGAS; and
(2) Other Certified Benzene-FRGAS
produced at a different refinery.
(3) The independent third party shall
submit a report:
(i) To the foreign refiner containing
the information required under
paragraphs (f)(1) and (f)(2) of this
section, to accompany the product
transfer documents for the vessel; and
(ii) To the Administrator containing
the information required under
paragraphs (f)(1) and (f)(2) of this
section, within thirty days following the
date of the independent third party’s
inspection. This report shall include a
description of the method used to
determine the identity of the refinery at
which the gasoline was produced,
assurance that the gasoline remained
segregated as specified in paragraph
(n)(1) of this section, and a description
of the gasoline’s movement and storage
between production at the source
refinery and vessel loading.
(4) The independent third party must:
(i) Be approved in advance by EPA,
based on a demonstration of ability to
perform the procedures required in this
paragraph (f);
(ii) Be independent under the criteria
specified in § 80.65(e)(2)(iii); and
(iii) Sign a commitment that contains
the provisions specified in paragraph (i)
of this section with regard to activities,
facilities and documents relevant to
compliance with the requirements of
this paragraph (f).
(g) Comparison of load port and port
of entry testing. (1)(i) Any foreign refiner
and any United States importer of
Certified Benzene-FRGAS shall compare
the results from the load port testing
under paragraph (f) of this section, with
the port of entry testing as reported
under paragraph (o) of this section, for
the volume of gasoline and the benzene
content value; except as specified in
paragraph (g)(1)(ii) of this section.
(ii) Where a vessel transporting
Certified Benzene-FRGAS off loads this
gasoline at more than one United States
port of entry, and the conditions of
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paragraph (g)(2)(i) of this section are met
at the first United States port of entry,
the requirements of paragraph (g)(2) of
this section do not apply at subsequent
ports of entry if the United States
importer obtains a certification from the
vessel owner that meets the
requirements of paragraph(s) of this
section, that the vessel has not loaded
any gasoline or blendstock between the
first United States port of entry and the
subsequent port of entry.
(2)(i) The requirements of this
paragraph (g)(2) apply if—
(A) The temperature-corrected
volumes determined at the port of entry
and at the load port differ by more than
one percent; or
(B) The benzene content value
determined at the port of entry is higher
than the benzene content value
determined at the load port, and the
amount of this difference is greater than
the reproducibility amount specified for
the port of entry test result by the
American Society of Testing and
Materials (ASTM) for the test method
specified at § 80.46(e).
(ii) The United States importer and
the foreign refiner shall treat the
gasoline as Non-Certified BenzeneFRGAS, and the foreign refiner shall
exclude the gasoline volume from its
gasoline volumes calculations and
benzene standard designations under
this subpart.
(h) Attest requirements. Refiners, for
each annual compliance period, must
arrange to have an attest engagement
performed of the underlying
documentation that forms the basis of
any report required under this subpart.
The attest engagement must comply
with the procedures and requirements
that apply to refiners under §§ 80.125
through 80.130, or other applicable
attest engagement provisions, and must
be submitted to the Administrator of
EPA by August 31 of each year for the
prior annual compliance period. The
following additional procedures shall be
carried out for any foreign refiner of
Benzene-FRGAS.
(1) The inventory reconciliation
analysis under § 80.128(b) and the
tender analysis under § 80.128(c) shall
include Non-Benzene-FRGAS.
(2) Obtain separate listings of all
tenders of Certified Benzene-FRGAS
and of Non-Certified Benzene-FRGAS,
and obtain separate listings of Certified
Benzene-FRGAS based on whether it is
small refiner gasoline, gasoline
produced through the use of credits, or
other applicable designation under this
subpart. Agree the total volume of
tenders from the listings to the gasoline
inventory reconciliation analysis in
§ 80.128(b), and to the volumes
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determined by the third party under
paragraph (f)(1) of this section.
(3) For each tender under paragraph
(h)(2) of this section, where the gasoline
is loaded onto a marine vessel, report as
a finding the name and country of
registration of each vessel, and the
volumes of Benzene-FRGAS loaded onto
each vessel.
(4) Select a sample from the list of
vessels identified in paragraph (h)(3) of
this section used to transport Certified
Benzene-FRGAS, in accordance with the
guidelines in § 80.127, and for each
vessel selected perform the following:
(i) Obtain the report of the
independent third party, under
paragraph (f) of this section, and of the
United States importer under paragraph
(o) of this section.
(A) Agree the information in these
reports with regard to vessel
identification, gasoline volumes and
benzene content test results.
(B) Identify, and report as a finding,
each occasion the load port and port of
entry benzene content and volume
results differ by more than the amounts
allowed in paragraph (g) of this section,
and determine whether the foreign
refiner adjusted its refinery calculations
as required in paragraph (g) of this
section.
(ii) Obtain the documents used by the
independent third party to determine
transportation and storage of the
Certified Benzene-FRGAS from the
refinery to the load port, under
paragraph (f) of this section. Obtain tank
activity records for any storage tank
where the Certified Benzene-FRGAS is
stored, and pipeline activity records for
any pipeline used to transport the
Certified Benzene-FRGAS, prior to being
loaded onto the vessel. Use these
records to determine whether the
Certified Benzene-FRGAS was produced
at the refinery that is the subject of the
attest engagement, and whether the
Certified Benzene-FRGAS was mixed
with any Non-Certified BenzeneFRGAS, Non-Benzene-FRGAS, or any
Certified Benzene-FRGAS produced at a
different refinery.
(5) Select a sample from the list of
vessels identified in paragraph (h)(3) of
this section used to transport Certified
and Non-Certified Benzene-FRGAS, in
accordance with the guidelines in
§ 80.127, and for each vessel selected
perform the following:
(i) Obtain a commercial document of
general circulation that lists vessel
arrivals and departures, and that
includes the port and date of departure
of the vessel, and the port of entry and
date of arrival of the vessel.
(ii) Agree the vessel’s departure and
arrival locations and dates from the
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independent third party and United
States importer reports to the
information contained in the
commercial document.
(6) Obtain separate listings of all
tenders of Non-Benzene-FRGAS, and
perform the following:
(i) Agree the total volume and
benzene content of tenders from the
listings to the gasoline inventory
reconciliation analysis in § 80.128(b).
(ii) Obtain a separate listing of the
tenders under this paragraph (h)(6)
where the gasoline is loaded onto a
marine vessel. Select a sample from this
listing in accordance with the
guidelines in § 80.127, and obtain a
commercial document of general
circulation that lists vessel arrivals and
departures, and that includes the port
and date of departure and the ports and
dates where the gasoline was off loaded
for the selected vessels. Determine and
report as a finding the country where
the gasoline was off loaded for each
vessel selected.
(7) In order to complete the
requirements of this paragraph (h) an
auditor shall:
(i) Be independent of the foreign
refiner;
(ii) Be licensed as a Certified Public
Accountant in the United States and a
citizen of the United States, or be
approved in advance by EPA based on
a demonstration of ability to perform the
procedures required in §§ 80.125
through 80.130 and this paragraph (h);
and
(iii) Sign a commitment that contains
the provisions specified in paragraph (i)
of this section with regard to activities
and documents relevant to compliance
with the requirements of §§ 80.125
through 80.130 and this paragraph (h).
(i) Foreign refiner commitments. Any
foreign refiner shall commit to and
comply with the provisions contained
in this paragraph (i) as a condition to
being approved for as a foreign refiner
under this subpart.
(1) Any United States Environmental
Protection Agency inspector or auditor
must be given full, complete and
immediate access to conduct
inspections and audits of the foreign
refinery.
(i) Inspections and audits may be
either announced in advance by EPA, or
unannounced.
(ii) Access will be provided to any
location where:
(A) Gasoline is produced;
(B) Documents related to refinery
operations are kept;
(C) Gasoline or blendstock samples
are tested or stored; and
(D) Benzene-FRGAS is stored or
transported between the foreign refinery
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and the United States, including storage
tanks, vessels and pipelines.
(iii) Inspections and audits may be by
EPA employees or contractors to EPA.
(iv) Any documents requested that are
related to matters covered by
inspections and audits must be
provided to an EPA inspector or auditor
on request.
(v) Inspections and audits by EPA
may include review and copying of any
documents related to:
(A) Refinery baseline establishment, if
applicable, including the volume and
benzene content of gasoline; transfers of
title or custody of any gasoline or
blendstocks whether Benzene-FRGAS or
Non-Benzene-FRGAS, produced at the
foreign refinery during the period
January 1, 2004 through December 31,
2005, and any work papers related to
refinery baseline establishment;
(B) The volume and benzene content
of Benzene-FRGAS;
(C) The proper classification of
gasoline as being Benzene-FRGAS or as
not being Benzene-FRGAS, or as
Certified Benzene-FRGAS or as NonCertified Benzene-FRGAS, and all other
relevant designations under this
subpart;
(D) Transfers of title or custody to
Benzene-FRGAS;
(E) Sampling and testing of BenzeneFRGAS;
(F) Work performed and reports
prepared by independent third parties
and by independent auditors under the
requirements of this section, including
work papers; and
(G) Reports prepared for submission
to EPA, and any work papers related to
such reports.
(vi) Inspections and audits by EPA
may include taking samples of gasoline,
gasoline additives or blendstock, and
interviewing employees.
(vii) Any employee of the foreign
refiner must be made available for
interview by the EPA inspector or
auditor, on request, within a reasonable
time period.
(viii) English language translations of
any documents must be provided to an
EPA inspector or auditor, on request,
within 10 working days.
(ix) English language interpreters
must be provided to accompany EPA
inspectors and auditors, on request.
(2) An agent for service of process
located in the District of Columbia shall
be named, and service on this agent
constitutes service on the foreign refiner
or any employee of the foreign refiner
for any action by EPA or otherwise by
the United States related to the
requirements of this subpart.
(3) The forum for any civil or criminal
enforcement action related to the
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provisions of this section for violations
of the Clean Air Act or regulations
promulgated thereunder shall be
governed by the Clean Air Act,
including the EPA administrative forum
where allowed under the Clean Air Act.
(4) United States substantive and
procedural laws shall apply to any civil
or criminal enforcement action against
the foreign refiner or any employee of
the foreign refiner related to the
provisions of this section.
(5) Submitting a petition for
participation in the benzene foreign
refiner program or producing and
exporting gasoline under any such
program, and all other actions to comply
with the requirements of this subpart
relating to participation in any benzene
foreign refiner program, or to establish
an individual refinery gasoline benzene
baseline under this subpart constitute
actions or activities covered by and
within the meaning of the provisions of
28 U.S.C. 1605(a)(2), but solely with
respect to actions instituted against the
foreign refiner, its agents and employees
in any court or other tribunal in the
United States for conduct that violates
the requirements applicable to the
foreign refiner under this subpart,
including conduct that violates the
False Statements Accountability Act of
1996 (18 U.S.C. 1001) and section
113(c)(2) of the Clean Air Act (42 U.S.C.
7413).
(6) The foreign refiner, or its agents or
employees, will not seek to detain or to
impose civil or criminal remedies
against EPA inspectors or auditors,
whether EPA employees or EPA
contractors, for actions performed
within the scope of EPA employment
related to the provisions of this section.
(7) The commitment required by this
paragraph (i) shall be signed by the
owner or president of the foreign refiner
business.
(8) In any case where Benzene-FRGAS
produced at a foreign refinery is stored
or transported by another company
between the refinery and the vessel that
transports the Benzene-FRGAS to the
United States, the foreign refiner shall
obtain from each such other company a
commitment that meets the
requirements specified in paragraphs
(i)(1) through (7) of this section, and
these commitments shall be included in
the foreign refiner’s petition to
participate in any benzene foreign
refiner program.
(j) Sovereign immunity. By submitting
a petition for participation in any
benzene foreign refiner program under
this subpart (and baseline, if applicable)
under this section, or by producing and
exporting gasoline to the United States
under any such program, the foreign
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refiner, and its agents and employees,
without exception, become subject to
the full operation of the administrative
and judicial enforcement powers and
provisions of the United States without
limitation based on sovereign immunity,
with respect to actions instituted against
the foreign refiner, its agents and
employees in any court or other tribunal
in the United States for conduct that
violates the requirements applicable to
the foreign refiner under this subpart,
including conduct that violates the
False Statements Accountability Act of
1996 (18 U.S.C. 1001) and section
113(c)(2) of the Clean Air Act (42 U.S.C.
7413).
(k) Bond posting. Any foreign refiner
shall meet the requirements of this
paragraph (k) as a condition to approval
as benzene foreign refiner under this
subpart.
(1) The foreign refiner shall post a
bond of the amount calculated using the
following equation:
Bond = G × $ 0.01
Where:
Bond = amount of the bond in U.S.
dollars
G = the largest volume of gasoline
produced at the foreign refinery and
exported to the United States, in
gallons, during a single calendar
year among the most recent of the
following calendar years, up to a
maximum of five calendar years:
the calendar year immediately
preceding the date the refinery’s
baseline petition is submitted, the
calendar year the baseline petition
is submitted, and each succeeding
calendar year.
(2) Bonds shall be posted by:
(i) Paying the amount of the bond to
the Treasurer of the United States;
(ii) Obtaining a bond in the proper
amount from a third party surety agent
that is payable to satisfy United States
administrative or judicial judgments
against the foreign refiner, provided
EPA agrees in advance as to the third
party and the nature of the surety
agreement; or
(iii) An alternative commitment that
results in assets of an appropriate
liquidity and value being readily
available to the United States, provided
EPA agrees in advance as to the
alternative commitment.
(3) Bonds posted under this paragraph
(k) shall—
(i) Be used to satisfy any judicial
judgment that results from an
administrative or judicial enforcement
action for conduct in violation of this
subpart, including where such conduct
violates the False Statements
Accountability Act of 1996 (18 U.S.C.
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1001) and section 113(c)(2) of the Clean
Air Act (42 U.S.C. 7413);
(ii) Be provided by a corporate surety
that is listed in the United States
Department of Treasury Circular 570
‘‘Companies Holding Certificates of
Authority as Acceptable Sureties on
Federal Bonds’’; and
(iii) Include a commitment that the
bond will remain in effect for at least
five years following the end of latest
annual reporting period that the foreign
refiner produces gasoline pursuant to
the requirements of this subpart.
(4) On any occasion a foreign refiner
bond is used to satisfy any judgment,
the foreign refiner shall increase the
bond to cover the amount used within
90 days of the date the bond is used.
(5) If the bond amount for a foreign
refiner increases, the foreign refiner
shall increase the bond to cover the
shortfall within 90 days of the date the
bond amount changes. If the bond
amount decreases, the foreign refiner
may reduce the amount of the bond
beginning 90 days after the date the
bond amount changes.
(l) [Reserved]
(m) English language reports. Any
report or other document submitted to
EPA by a foreign refiner shall be in
English language, or shall include an
English language translation.
(n) Prohibitions. (1) No person may
combine Certified Benzene-FRGAS with
any Non-Certified Benzene-FRGAS or
Non-Benzene-FRGAS, and no person
may combine Certified Benzene-FRGAS
with any Certified Benzene-FRGAS
produced at a different refinery, until
the importer has met all the
requirements of paragraph (o) of this
section, except as provided in paragraph
(e) of this section.
(2) No foreign refiner or other person
may cause another person to commit an
action prohibited in paragraph (n)(1) of
this section, or that otherwise violates
the requirements of this section.
(o) United States importer
requirements. Any United States
importer shall meet the following
requirements:
(1) Each batch of imported gasoline
shall be classified by the importer as
being Benzene-FRGAS or as NonBenzene-FRGAS, and each batch
classified as Benzene-FRGAS shall be
further classified as Certified BenzeneFRGAS or as Non-Certified BenzeneFRGAS.
(2) Gasoline shall be classified as
Certified Benzene-FRGAS or as NonCertified Benzene-FRGAS according to
the designation by the foreign refiner if
this designation is supported by product
transfer documents prepared by the
foreign refiner as required in paragraph
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(d) of this section, unless the gasoline is
classified as Non-Certified BenzeneFRGAS under paragraph (g) of this
section. Additionally, the importer shall
comply with all requirements of this
subpart applicable to importers.
(3) For each gasoline batch classified
as Benzene-FRGAS, any United States
importer shall perform the following
procedures.
(i) In the case of both Certified and
Non-Certified Benzene-FRGAS, have an
independent third party:
(A) Determine the volume of gasoline
in the vessel;
(B) Use the foreign refiner’s BenzeneFRGAS certification to determine the
name and EPA-assigned registration
number of the foreign refinery that
produced the Benzene-FRGAS;
(C) Determine the name and country
of registration of the vessel used to
transport the Benzene-FRGAS to the
United States; and
(D) Determine the date and time the
vessel arrives at the United States port
of entry.
(ii) In the case of Certified BenzeneFRGAS, have an independent third
party:
(A) Collect a representative sample
from each vessel compartment
subsequent to the vessel’s arrival at the
United States port of entry and prior to
off loading any gasoline from the vessel;
(B) Obtain the compartment samples;
and
(C) Determine the benzene content
value of each compartment sample
using the methodology specified at
80.46(e) by the third party analyzing the
sample or by the third party observing
the importer analyze the sample.
(4) Any importer shall submit reports
within 30 days following the date any
vessel transporting Benzene-FRGAS
arrives at the United States port of entry:
(i) To the Administrator containing
the information determined under
paragraph (o)(3) of this section; and
(ii) To the foreign refiner containing
the information determined under
paragraph (o)(3)(ii) of this section, and
including identification of the port at
which the product was offloaded.
(5) Any United States importer shall
meet all other requirements of this
subpart, for any imported gasoline that
is not classified as Certified BenzeneFRGAS under paragraph (o)(2) of this
section.
(p) Truck imports of Certified
Benzene-FRGAS produced at a foreign
refinery. (1) Any refiner whose Certified
Benzene-FRGAS is transported into the
United States by truck may petition EPA
to use alternative procedures to meet the
following requirements:
(i) Certification under paragraph (d)(5)
of this section;
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(ii) Load port and port of entry
sampling and testing under paragraphs
(f) and (g) of this section;
(iii) Attest under paragraph (h) of this
section; and
(iv) Importer testing under paragraph
(o)(3) of this section.
(2) These alternative procedures must
ensure Certified Benzene-FRGAS
remains segregated from Non-Certified
Benzene-FRGAS and from NonBenzene-FRGAS until it is imported
into the United States. The petition will
be evaluated based on whether it
adequately addresses the following:
(i) Provisions for monitoring pipeline
shipments, if applicable, from the
refinery, that ensure segregation of
Certified Benzene-FRGAS from that
refinery from all other gasoline;
(ii) Contracts with any terminals and/
or pipelines that receive and/or
transport Certified Benzene-FRGAS, that
prohibit the commingling of Certified
Benzene-FRGAS with any of the
following:
(A) Other Certified Benzene-FRGAS
from other refineries.
(B) All Non-Certified BenzeneFRGAS.
(C) All Non-Benzene-FRGAS;
(iii) Procedures for obtaining and
reviewing truck loading records and
United States import documents for
Certified Benzene-FRGAS to ensure that
such gasoline is only loaded into trucks
making deliveries to the United States;
(iv) Attest procedures to be conducted
annually by an independent third party
that review loading records and import
documents based on volume
reconciliation, or other criteria, to
confirm that all Certified BenzeneFRGAS remains segregated throughout
the distribution system and is only
loaded into trucks for import into the
United States.
(3) The petition required by this
section must be submitted to EPA along
with the application for temporary
refiner relief individual refinery
benzene standard under this subpart.
(q) Withdrawal or suspension of
foreign refiner status. EPA may
withdraw or suspend a foreign refiner’s
benzene baseline or standard approval
for a foreign refinery where—
(1) A foreign refiner fails to meet any
requirement of this section;
(2) A foreign government fails to
allow EPA inspections as provided in
paragraph (i)(1) of this section;
(3) A foreign refiner asserts a claim of,
or a right to claim, sovereign immunity
in an action to enforce the requirements
in this subpart; or
(4) A foreign refiner fails to pay a civil
or criminal penalty that is not satisfied
using the foreign refiner bond specified
in paragraph (k) of this section.
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(r) Early use of a foreign refiner
benzene baseline. (1) A foreign refiner
may begin using an individual refinery
benzene baseline under this subpart
before EPA has approved the baseline,
provided that:
(i) A baseline petition has been
submitted as required in paragraph (b)
of this section;
(ii) EPA has made a provisional
finding that the baseline petition is
complete;
(iii) The foreign refiner has made the
commitments required in paragraph (i)
of this section;
(iv) The persons that will meet the
independent third party and
independent attest requirements for the
foreign refinery have made the
commitments required in paragraphs
(f)(3)(iii) and (h)(7)(iii) of this section;
and
(v) The foreign refiner has met the
bond requirements of paragraph (k) of
this section.
(2) In any case where a foreign refiner
uses an individual refinery baseline
before final approval under paragraph
(r)(1) of this section, and the foreign
refinery baseline values that ultimately
are approved by EPA are more stringent
than the early baseline values used by
the foreign refiner, the foreign refiner
shall recalculate its compliance, ab
initio, using the baseline values
approved by the EPA, and the foreign
refiner shall be liable for any resulting
violation of the requirements of this
subpart.
(s) Additional requirements for
petitions, reports and certificates. Any
petition for approval to produce
gasoline subject to the benzene foreign
refiner program, any alternative
procedures under paragraph (p) of this
section, any report or other submission
required by paragraph (c), (f)(2), or (i) of
this section, and any certification under
paragraph (d)(3) of this section shall
be—
(1) Submitted in accordance with
procedures specified by the
Administrator, including use of any
forms that may be specified by the
Administrator.
(2) Be signed by the president or
owner of the foreign refiner company, or
by that person’s immediate designee,
and shall contain the following
declaration:
I hereby certify: (1) That I have actual
authority to sign on behalf of and to bind
[insert name of foreign refiner] with regard to
all statements contained herein; (2) that I am
aware that the information contained herein
is being Certified, or submitted to the United
States Environmental Protection Agency,
under the requirements of 40 CFR part 80,
subpart L, and that the information is
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material for determining compliance under
these regulations; and (3) that I have read and
understand the information being Certified or
submitted, and this information is true,
complete and correct to the best of my
knowledge and belief after I have taken
reasonable and appropriate steps to verify the
accuracy thereof. I affirm that I have read and
understand the provisions of 40 CFR part 80,
subpart L, including 40 CFR 80.1420 apply
to [insert name of foreign refiner]. Pursuant
to Clean Air Act section 113(c) and 18 U.S.C.
1001, the penalty for furnishing false,
incomplete or misleading information in this
certification or submission is a fine of up to
$10,000 U.S., and/or imprisonment for up to
five years.
PART 85—CONTROL OF AIR
POLLUTION FROM MOBILE SOURCES
10. The authority citation for part 85
continues to read as follows:
Authority: 42 U.S.C. 7401–7671q.
Subpart P—[Amended]
11. Section 85.1515 is amended by
adding paragraphs (c)(2)(vii), (c)(2)(viii),
and (c)(8) to read as follows.
§ 85.1515 Emission standards and test
procedures applicable to imported
nonconforming motor vehicles and motor
vehicle engines.
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(2) * * *
(vii) Nonconforming LDV/LLDTs
originally manufactured in OP years
2009 and later must meet the
evaporative emission standards in Table
S09–1 in 40 CFR 86.1811–09(e).
However, LDV/LLDTs originally
manufactured in OP years 2009 and
2010 and imported by ICIs who qualify
as small volume manufacturers as
defined in 40 CFR 86.1838–01 are
exempt from the LDV/LLDT evaporative
emission standards in Table S09–1 in 40
CFR 86.1811–09(e), but must comply
with the Tier 2 evaporative emission
standards in Table S04–3 in 40 CFR
86.1811–04(e).
(viii) Nonconforming HLDTs and
MDPVs originally manufactured in OP
years 2010 and later must meet the
evaporative emission standards in Table
S09–1 in 40 CFR 86.1811–09(e).
However, HLDTs and MDPVs originally
manufactured in OP years 2010 and
2011 and imported by ICIs, who qualify
as small volume manufacturers as
defined in 40 CFR 86.1838–01, are
exempt from the HLDTs and MDPVs
evaporative emission standards in Table
S09–1 in 40 CFR 86.1811–09(e), but
must comply with the Tier 2
evaporative emission standards in Table
S04–3 in 40 CFR 86.1811–04(e).
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(8)(i) Nonconforming LDV/LLDTs
originally manufactured in OP years
2010 and later must meet the cold
temperature NHMC emission standards
in Table S10–1 in 40 CFR 86.1811–
10(g).
(ii) Nonconforming HLDTs and
MDPVs originally manufactured in OP
years 2012 and later must meet the cold
temperature NHMC emission standards
in Table S10–1 in 40 CFR 86.1811–
10(g).
(iii) ICIs, which qualify as small
volume manufacturers, are exempt from
the cold temperature NMHC phase-in
intermediate percentage requirements
described in 40 CFR 86.1811–10(g)(3).
See 40 CFR 86.1811–04(k)(5)(vi) and
(vii).
(iv) As an alternative to the
requirements of paragraphs (c)(8)(i) and
(ii) of this section, ICIs may elect to
meet a cold temperature NMHC family
emission level below the cold
temperature NMHC fleet average
standards specified in Table S10–1 of 40
CFR 86.1811–10 and bank or sell credits
as permitted in 40 CFR 86.1864–10. An
ICI may not meet a higher cold
temperature NMHC family emission
level than the fleet average standards in
Table S10–1 of 40 CFR 86.1811–10 as
specified in paragraphs (c)(8)(i) and (ii)
of this section, unless it demonstrates to
the Administrator at the time of
certification that it has obtained
appropriate and sufficient NMHC
credits from another manufacturer, or
has generated them in a previous model
year or in the current model year and
not traded them to another
manufacturer or used them to address
other vehicles as permitted in 40 CFR
86.1864–10.
(v) Where an ICI desires to obtain a
certificate of conformity using a higher
cold temperature NMHC family
emission level than specified in
paragraphs (c)(8)(i) and (ii) of this
section, but does not have sufficient
credits to cover vehicles imported under
such certificate, the Administrator may
issue such certificate if the ICI has also
obtained a certificate of conformity for
vehicles certified using a cold
temperature NMHC family emission
level lower than that required under
paragraphs (c)(8)(i) and (ii) of this
section. The ICI may then import
vehicles to the higher cold temperature
NMHC family emission level only to the
extent that it has generated sufficient
credits from vehicles certified to a
family emission level lower than the
cold temperature NMHC fleet average
standard during the same model year.
(vi) ICIs using cold temperature
NMHC family emission levels higher
than the cold temperature NMHC fleet
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15953
average standards specified in
paragraphs (c)(8)(i) and (ii) of this
section must monitor their imports so
that they do not import more vehicles
certified to such family emission levels
than their available credits can cover.
ICIs must not have a credit deficit at the
end of a model year and are not
permitted to use the deficit carryforward
provisions provided in 40 CFR 86.1864–
10.
(vii) The Administrator may condition
the certificates of conformity issued to
ICIs as necessary to ensure that vehicles
subject to this paragraph (c)(8) comply
with the applicable cold temperature
NMHC fleet average standard for each
model year.
*
*
*
*
*
PART 86—CONTROL OF EMISSIONS
FROM NEW AND IN-USE HIGHWAY
VEHICLES AND ENGINES
12. The authority citation for part 86
continues to read as follows:
Authority: 42 U.S.C. 7401–7671q.
Subpart H—[Amended]
13. Section 86.701–94 is amended by
revising paragraph (a) to read as follows:
§ 86.701–94
General applicability.
(a) The provisions of this subpart
apply to: 1994 through 2003 model year
Otto-cycle and diesel light-duty
vehicles; 1994 through 2003 model year
Otto-cycle and diesel light-duty trucks;
and 1994 and later model year Ottocycle and diesel heavy-duty engines;
and 2001 and later model year Ottocycle heavy-duty vehicles and engines
certified under the provisions of subpart
S of this part. The provisions of subpart
B of this part apply to this subpart. The
provisions of § 86.1811–04(a)(5) and (p)
apply to 2004 and later model year
light-duty vehicles, light-duty trucks,
and medium duty passenger vehicles.
*
*
*
*
*
Subpart S—[Amended]
14. Section 86.1803–01 is amended by
revising the definition of ‘‘Banking’’ and
adding the definition for ‘‘Fleet average
cold temperature NMHC standard’’ to
read as follows:
§ 86.1803–01
*
Definitions.
*
*
*
*
Banking means one of the following:
(1) The retention of NOX emission
credits for complete heavy-duty vehicles
by the manufacturer generating the
emission credits, for use in future model
year certification programs as permitted
by regulation.
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(2) The retention of cold temperature
non-methane hydrocarbon (NMHC)
emission credits for light-duty vehicles,
light-duty trucks, and medium-duty
passenger vehicles by the manufacturer
generating the emission credits, for use
in future model year certification
programs as permitted by regulation.
*
*
*
*
*
Fleet average cold temperature NMHC
standard means, for light-duty vehicles,
light-duty trucks and medium-duty
passenger vehicles, an NMHC cold
temperature standard imposed over an
individual manufacturer’s total 50-State
U.S. sales (or a fraction of total U.S.
sales during phase-in years), as ‘‘U.S.
sales’’ is defined to include all national
sales, including points-of-first sale in
California, of a given model year.
Manufacturers determine their
compliance with such a standard by
averaging, on a sales-weighted basis, the
individual NMHC ‘‘Family Emission
Limits’’ (FEL—as defined in this
subpart) to which light-duty vehicles,
light-duty trucks and medium-duty
passenger vehicles were certified and
sold for that model year.
*
*
*
*
*
15. Section 86.1805–04 is amended by
adding paragraph (g) to read as follows:
§ 86.1805–04
Useful life.
*
*
*
*
*
(g) Where cold temperature NMHC
standards are applicable, the useful life
requirement for compliance with the
cold temperature NMHC standard only
is as follows:
(1) For LDV/LLDTs, 10 years or
120,000 miles, whichever occurs first.
(2) For HLDT/MDPVs, 11 years or
120,000 miles, whichever occurs first.
16. A new § 86.1809–10 is added to
Subpart S to read as follows:
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§ 86.1809–10
Prohibition of defeat devices.
(a) No new light-duty vehicle, lightduty truck, medium-duty passenger
vehicle, or complete heavy-duty vehicle
shall be equipped with a defeat device.
(b) The Administrator may test or
require testing on any vehicle at a
designated location, using driving
cycles and conditions which may
reasonably be expected to be
encountered in normal operation and
use, for the purposes of investigating a
potential defeat device.
(c) For cold temperature CO and cold
temperature NMHC emission control,
the Administrator will use a guideline
to determine the appropriateness of the
CO and NMHC emission control at
ambient temperatures between 25 °F (4
°C) (the upper bound of the cold test
range) and 68 °F (20 °C) (the lower
bound of the FTP range). The guideline
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for CO emission congruity across the
intermediate temperature range is the
linear interpolation between the CO
standard applicable at 25 °F (4 °C) and
the CO standard applicable at 68 °F (20
°C). The guideline for NMHC emission
congruity across the intermediate
temperature range is the linear
interpolation between the NMHC FEL
applicable at 25 °F (4 °C) and the Tier
2 NMOG standard to which the vehicle
was certified at 68 °F (20 °C), where the
intermediate temperature NMHC level is
rounded to the nearest hundredth for
comparison to the interpolated line. For
vehicles that exceed this CO emissions
guideline or this NMHC emissions
guideline upon intermediate
temperature cold testing:
(1) If the CO emission level is greater
than the 20 °F (7 °C) emission standard,
the vehicle will automatically be
considered to be equipped with a defeat
device without further investigation. If
the intermediate temperature NMHC
emission level, rounded to the nearest
hundredth, is greater than the 20 °F (7
°C) FEL, the vehicle will automatically
be considered to be equipped with a
defeat device without further
investigation.
(2) If the CO emission level does not
exceed the 20 °F emission standard, the
Administrator may investigate the
vehicle design for the presence of a
defeat device under paragraph (d) of this
section. If the intermediate temperature
NMHC emission level, rounded to the
nearest hundredth, does not exceed the
20 °F FEL, the Administrator may
investigate the vehicle design for the
presence of a defeat device under
paragraph (d) of this section.
(d) For vehicle designs designated by
the Administrator to be investigated for
possible defeat devices:
(1) The manufacturer must show to
the satisfaction of the Administrator that
the vehicle design does not incorporate
strategies that unnecessarily reduce
emission control effectiveness exhibited
during the Federal or Supplemental
Federal emissions test procedures (FTP
or SFTP) when the vehicle is operated
under conditions which may reasonably
be expected to be encountered in
normal operation and use.
(2) The following information
requirements apply:
(i) Upon request by the Administrator,
the manufacturer will provide an
explanation containing detailed
information regarding test programs,
engineering evaluations, design
specifications, calibrations, on-board
computer algorithms, and design
strategies incorporated for operation
both during and outside of the Federal
emission test procedure.
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(ii) For purposes of investigations of
possible cold temperature CO or cold
temperature NMHC defeat devices
under this paragraph (d), the
manufacturer shall provide an
explanation which must show, to the
satisfaction of the Administrator, that
CO emissions and NMHC emissions are
reasonably controlled in reference to the
linear guideline across the intermediate
temperature range.
(e) For each test group of Tier 2 LDV/
LLDTs and HLDT/MDPVs and interim
non-Tier 2 LDV/LLDTs and HLDT/
MDPVs the manufacturer must submit,
with the Part II certification application,
an engineering evaluation
demonstrating to the satisfaction of the
Administrator that a discontinuity in
emissions of non-methane organic gases,
carbon monoxide, oxides of nitrogen
and formaldehyde measured on the
Federal Test Procedure (subpart B of
this part) does not occur in the
temperature range of 20 to 86 degrees F.
For diesel vehicles, the engineering
evaluation must also include particulate
emissions.
17. A new § 86.1810–09 is added to
Subpart S to read as follows:
§ 86.1810–09 General standards; increase
in emissions; unsafe condition; waivers.
Section 86.1810–09 includes text that
specifies requirements that differ from
§ 86.1810–01. Where a paragraph in
§ 86.1810–01 is identical and applicable
to § 86.1810–09, this may be indicated
by specifying the corresponding
paragraph and the statement
‘‘[Reserved]. For guidance see
§ 86.1810–01.’’ Where a corresponding
paragraph of § 86.1810–01 is not
applicable, this is indicated by the
statement ‘‘[Reserved].’’ This section
applies to model year 2009 and later
light-duty vehicles and light-duty trucks
fueled by gasoline, diesel, methanol,
ethanol, natural gas and liquefied
petroleum gas fuels. This section also
applies to MDPVs and complete heavyduty vehicles certified according to the
provisions of this subpart. Multi-fueled
vehicles (including dual-fueled and
flexible-fueled vehicles) shall comply
with all requirements established for
each consumed fuel (or blend of fuels in
the case of flexible fueled vehicles). The
standards of this subpart apply to both
certification and in-use vehicles unless
otherwise indicated. This section also
applies to hybrid electric vehicles and
zero emission vehicles. Unless
otherwise specified, requirements and
provisions of this subpart applicable to
methanol fueled vehicles are also
applicable to Tier 2 and interim nonTier 2 ethanol fueled vehicles.
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(a) through (e) [Reserved]. For
guidance see § 86.1810–01.
(f) Altitude requirements. (1) All
emission standards apply at low altitude
conditions and at high altitude
conditions, except for supplemental
exhaust emission standards, cold
temperature NMHC emission standards,
and the evaporative emission standards
as described in § 86.1811–09(e).
Supplemental exhaust emission
standards, as described in § 86.1811–
04(f), apply only at low altitude
conditions. Cold temperature NMHC
emission standards, as described in
§ 86.1811–10(g), apply only at low
altitude conditions. Tier 2 evaporative
emission standards apply at high
altitude conditions as specified in
§ 86.1810–01(f) and (j), and § 86.1811–
04(e).
(2) For vehicles that comply with the
cold temperature NMHC standards,
manufacturers shall submit an
engineering evaluation indicating that
common calibration approaches are
utilized at high altitudes. Any deviation
from low altitude emission control
practices shall be included in the
auxiliary emission control device
(AECD) descriptions submitted at
certification. Any AECD specific to high
altitude shall require engineering
emission data for EPA evaluation to
quantify any emission impact and
validity of the AECD.
(g) through (p) [Reserved]. For
guidance see § 86.1810–01.
18. Section 86.1811–04 is amended by
adding paragraphs (k)(5)(iv) through
(vii) and (q)(1)(vi) through (ix) to read as
follows:
§ 86.1811–04 Emission standards for lightduty vehicles, light-duty trucks and
medium-duty passenger vehicles.
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*
(k) * * *
(5) * * *
(iv) Vehicles produced by small
volume manufacturers, as defined in
§ 86.1838–01, are exempt from the LDV/
LLDT evaporative emissions standards
in Table S09–1 of § 86.1811–09(e) for
model years 2009 and 2010, but must
comply with the Tier 2 evaporative
emission standards in Table S04–3 in
paragraph (e)(1) of this section for
model years 2009 and 2010.
(v) Vehicles produced by small
volume manufacturers, as defined in
§ 86.1838–01, are exempt from the
HLDT/MDPV evaporative emissions
standards in Table S09–1 of § 86.1811–
09(e) for model years 2010 and 2011,
but must comply with the Tier 2
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evaporative emission standards in Table
S04–3 in paragraph (e)(1) of this section
for model years 2010 and 2011.
(vi) Small volume manufacturers, as
defined in § 86.1838–01, are exempt
from the LDV/LLDT cold temperature
NMHC phase-in requirements in Table
S10–1 of § 86.1811–10(g) for model
years 2010, 2011, and 2012, but must
comply with the 100% requirement for
2013 and later model years for cold
temperature NMHC standards
(vii) Small volume manufacturers, as
defined in § 86.1838–01, are exempt
from the HLDT/MDPV cold temperature
NMHC phase-in requirements in Table
S10–1 of § 86.1811–10(g) for model
years 2012, 2013, and 2014, but must
comply with the 100% requirement for
2015 and later model years for cold
temperature NMHC standards.
*
*
*
*
*
(q) * * *
(1) * * *
(vi) Defer compliance with the LDV/
LLDT evaporative emissions standards
in Table S09–1 of § 86.1811–09(e) until
2013, and defer compliance with the
LDV/LLDT evaporative emissions
standards in Table S09–2 of § 86.1811–
09(e) until 2014. (The hardship relief
may be extended one additional model
year—2 model years total.)
(vii) Defer compliance with the
HLDT/MDPV evaporative emissions
standards in Table S09–1 of § 86.1811–
09(e) until 2014, and defer compliance
with the HLDT/MDPV evaporative
emissions standards in Table S09–2 of
§ 86.1811–09(e) until 2015. (The
hardship relief may be extended one
additional model year—2 model years
total.)
(viii) Defer 100% compliance with the
LDV/LLDT cold temperature NMHC
standards in Table S10–X of § 86.1811–
10(g) until 2015. (The hardship relief
may be extended one additional model
year—2 model years total.)
(ix) Defer 100% compliance with the
HLDT/MDPV cold temperature NMHC
standards in Table S10–X of § 86.1811–
10(g) until 2017. (The hardship relief
may be extended one additional model
year—2 model years total.)
*
*
*
*
*
19. A new § 86.1811–09 is added to
Subpart S to read as follows:
§ 86.1811–09 Emission standards for lightduty vehicles, light-duty trucks and
medium-duty passenger vehicles.
Section 86.1811–09 includes text that
specifies requirements that differ from
§ 86.1811–04. Where a paragraph in
§ 86.1811–04 is identical and applicable
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to § 86.1811–09, this may be indicated
by specifying the corresponding
paragraph and the statement
‘‘[Reserved]. For guidance see
§ 86.1811–04.’’ Where a corresponding
paragraph of § 86.1811–04 is not
applicable, this is indicated by the
statement ‘‘[Reserved].’’
(a) Applicability. (1) This section
contains regulations implementing
emission standards for all LDVs, LDTs
and MDPVs. This section applies to
2009 and later model year LDVs, LDTs
and MDPVs fueled by gasoline, diesel,
methanol, ethanol, natural gas and
liquefied petroleum gas fuels, except as
noted. Additionally, this section applies
to hybrid electric vehicles (HEVs) and
zero emission vehicles (ZEVs). Unless
otherwise specified, multi-fueled
vehicles must comply with all
requirements established for each
consumed fuel.
(2) through (4) [Reserved]. For
guidance see § 86.1811–04.
(5) The exhaust emission standards
and evaporative emission standards of
this section apply equally to
certification and in-use LDVs, LDTs and
MDPVs, unless otherwise specified. See
paragraph (t) of this section for interim
evaporative emission in-use standards
that are different than the certification
evaporative emission standards
specified in paragraph (e) of this
section.
(b) through (d) [Reserved]. For
guidance see § 86.1811–04.
(e) Evaporative emission standards.
Evaporative emissions from gasolinefueled, natural gas-fueled, liquefied
petroleum gas-fueled, ethanol-fueled
and methanol-fueled vehicles must not
exceed the standards in this paragraph
(e). The standards apply equally to
certification and in-use vehicles.
(1) Diurnal-plus-hot soak evaporative
hydrocarbon standards. (i)
Hydrocarbons for LDV/LLDTs, HLDTs
and MDPVs that are gasoline-fueled,
dedicated natural gas-fueled, dedicated
liquefied petroleum gas-fueled,
dedicated ethanol-fueled, dedicated
methanol-fueled and multi-fueled
vehicles when operating on gasoline
must not exceed the diurnal plus hot
soak standards shown in Table S09–1
for the full three diurnal test sequence
and for the supplemental two diurnal
test sequence. The standards apply
equally to certification and in-use
vehicles, except as otherwise specified
in paragraph (t) of this section. Table
S09–1 follows:
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TABLE S09–1.—LIGHT-DUTY DIURNAL PLUS HOT SOAK EVAPORATIVE EMISSION STANDARDS
[Grams per test]
Vehicle category
Model year
LDVs ............................................................................................................................................
LLDTs ..........................................................................................................................................
HLDTs ..........................................................................................................................................
MDPVs .........................................................................................................................................
(ii) Hydrocarbons for LDV/LLDTs,
HLDTs and MDPVs that are multi-fueled
vehicles operating on non-gasoline fuel
must not exceed the diurnal plus hot
soak standards shown in Table S09–2
for the full three diurnal test sequence
and for the supplemental two diurnal
test sequence. The standards apply
2009
2009
2010
2010
3 day
diurnal+hot
soak
0.50
0.65
0.90
1.00
Supplemental
2 day
diurnal+hot
soak
0.65
0.85
1.15
1.25
equally to certification and in-use
vehicles except as otherwise specified
in paragraph (t) of this section. Table
S09–2 follows:
TABLE S09–2.—LIGHT-DUTY DIURNAL PLUS HOT SOAK EVAPORATIVE EMISSION STANDARDS: NON-GASOLINE PORTION
OF MULTI-FUELED VEHICLES
[Grams per test]
Vehicle category
Model year
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LDVs ............................................................................................................................................
LLDTs ..........................................................................................................................................
HLDTs ..........................................................................................................................................
MDPVs .........................................................................................................................................
(2) through (6) [Reserved]. For
guidance see § 86.1811–04.
(f) through (s) [Reserved]. For
guidance see § 86.1811–04.
(t) Evaporative emission in-use
standards. (1) For LDVs and LLDTs
certified prior to the 2012 model year,
the Tier 2 LDV/LLDT evaporative
emissions standards in Table S04–3 of
§ 86.1811–04(e) shall apply to in-use
vehicles for only the first three model
years after an evaporative family is first
certified to the LDV/LLDT evaporative
emission standards in Table S09–1 of
paragraph (e) of this section. For
example, evaporative families first
certified to the LDV/LLDT standards in
Table S09–1 in the 2011 model year
shall meet the Tier 2 LDV/LLDT
evaporative emission standards (Table
S04–3) in-use for 2011, 2012, and 2013
model year vehicles (applying Tier 2
standards in-use is limited to the first
three years after introduction of a
vehicle).
(2) For HLDTs and MDPVs certified
prior to the 2013 model year, the Tier
2 HLDT/MDPV evaporative emissions
standards in Table S04–3 of § 86.1811–
04(e) shall apply to in-use vehicles for
only the first three model years after an
evaporative family is first certified to
the HLDT/MDPV evaporative emission
standards in Table S09–1 of paragraph
(e) of this section. For example,
evaporative families first certified to the
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HLDT/MDPV standards in Table S09–1
in the 2012 model year shall meet the
Tier 2 HLDT/MDPV evaporative
emission standards (Table S04–3) in-use
for 2012, 2013, and 2014 model year
vehicles (applying Tier 2 standards inuse is limited to the first three years
after introduction of a vehicle).
20. A new § 86.1811–10 is added to
Subpart S to read as follows:
§ 86.1811–10 Emission standards for lightduty vehicles, light-duty trucks and
medium-duty passenger vehicles.
Section 86.1811–10 includes text that
specifies requirements that differ from
§ 86.1811–04 and § 86.1811–09. Where a
paragraph in § 86.1811–04 or § 86.1811–
09 is identical and applicable to
§ 86.1811–10, this may be indicated by
specifying the corresponding paragraph
and the statement ‘‘[Reserved]. For
guidance see § 86.1811–04’’ or
‘‘[Reserved]. For guidance see
§ 86.1811–09.’’ Where a corresponding
paragraph of § 86.1811–04 or § 86.1811–
09 is not applicable, this is indicated by
the statement ‘‘[Reserved].’’
(a) [Reserved]. For guidance see
§ 86.1811–09.
(b) through (d) [Reserved]. For
guidance see § 86.1811–04.
(e) [Reserved]. For guidance see
§ 86.1811–09.
(f) [Reserved]. For guidance see
§ 86.1811–04.
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2012
2012
2013
2013
3 day
diurnal+hot
soak
0.50
0.65
0.90
1.00
Supplemental
2 day
diurnal+hot
soak
0.65
0.85
1.15
1.25
(g) Cold temperature exhaust
emission standards. (1) Cold
temperature CO standards. These cold
temperature CO standards are
applicable only to gasoline fueled LDV/
Ts and MDPVs. For the following cold
temperature CO exhaust emission
standards, a useful life of 50,000 miles
or 5 years (whichever occurs first)
applies:
(i) For LDVs and LDT1s, the standard
is 10.0 grams per mile CO.
(ii) For LDT2s, LDT3s and LDT4s, and
MDPVs the standard is 12.5 grams per
mile CO.
(iii) These standards do not apply to
interim non-Tier 2 MDPVs.
(2) Cold temperature NMHC
standards. Full useful life fleet average
cold temperature NMHC standards are
applicable only to gasoline fueled LDV/
LLDTs and HLDT/MDPVs, and apply
equally to certification and in-use
except as otherwise specified in
paragraph (u) of this section for in-use
standards for applicable phase-in
models. Testing with other fuels such as
E85, or testing on diesel vehicles, is not
required. Multi-fuel, bi-fuel or dual-fuel
vehicles must comply with
requirements using gasoline only. For
LDV/LLDTs, the useful life is 120,000
miles or 10 years, whichever comes
first. For HLDT/MDPVs, the useful life
is 120,000 miles or 11 years, whichever
comes first. There is not an intermediate
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useful life standard for cold temperature
NMHC standards.
(i) The standards are shown in Table
S10–1, which follows:
TABLE S10–2.—PHASE-IN PERCENT- products is at least 100% for model
AGES FOR LDV/LLDT COLD TEM- years 2010 and earlier for LDV/LLDTs,
and 2012 and earlier for HLDT/MDPVs.
PERATURE NMHC REQUIREMENTS
For example, a phase-in schedule for
LDV/LLDTs of 5/10/10/45/80/100 that
TABLE S10–1.—FLEET AVERAGE
begins in 2008 would calculate as (6 ×
Model year
5%) + (5 × 10%) + (4 × 10%) = 120%
COLD TEMPERATURE NMHC FULL
and would be acceptable for 2008–2010.
USEFUL LIFE EXHAUST EMISSION
The full phase-in would calculate as (6
STANDARDS
2010 ..................................
25
2011 ..................................
50 × 5%) + (5 × 10%) + (4 × 10%) + (3 ×
Cold temperature 2012 ..................................
75 45%) + (2 × 80%) + (1 × 100%) = 515%
NMHC sales2013 and subsequent .......
100 and would be acceptable for 2008–2013.
Vehicle weight category
weighted fleet
(iii) Under an alternate phase-in
average standard
schedule, the projected phase-in
(grams/mile)
TABLE S10–3.—PHASE-IN PERCENT- percentage is not binding for a given
AGES FOR HLDT/MDPV COLD TEM- model year, provided the sums of the
LDVs & LLDTs (≤ 6,000
actual phase-in percentages that occur
PERATURE NMHC REQUIREMENTS
lbs GVWR) ....................
0.3
meet the appropriate total sums as
HLDTs (>6,000–8,500 lbs
Percentage of required in the equations of paragraph
GVWR) & ......................
0.5
HLDT/MDPVs (g)(4)(i) of this section, and provided
MDPVs (>8,500 10,000
Model year
that must meet
lbs GVWR) .................... ............................
that 100% actual compliance is reached
requirement
for the appropriate model year, either
(ii) The manufacturer must calculate
2012 ......................................
25 2013 for LDV/LLDTs or 2015 for HLDT/
its fleet average cold temperature NMHC 2013 ......................................
50 MDPVs.
emission level(s) as described in
2014 ......................................
75
(5) Manufacturers must determine
§ 86.1864–10(m).
2015 and subsequent ...........
100 compliance with required phase-in
(iii) During a phase-in year, the
schedules as follows:
manufacturer must comply with the
(4) Alternate phase-in schedules for
(i) Manufacturers must submit
fleet average standards for the required
cold temperature NMHC standards. (i)
information showing compliance with
phase-in percentage for that year as
Manufacturers may apply for alternative all phase-in requirements of this section
specified in paragraph (g)(3) of this
phase-in schedules that would still
with their Part I applications as required
section, or for the alternate phase-in
result in 100% phase-in by 2013 and
by § 86.1844(d)(13).
percentage as permitted under
(ii) A manufacturer electing to use any
2015, respectively, for LDV/LLDTs and
paragraph (g)(4) of this section.
alternate phase-in schedule permitted
HLDT/MDPVs. An alternate phase-in
(iv) For model years prior to 2010
schedule submitted by a manufacturer is under this section must provide in its
(LDV/LLDTs) and 2012 (HLDT/MDPVs), subject to EPA approval. The alternative Application for Certification for the first
where the manufacturer desires to bank
year in which it intends to use such a
phase-in will not be used to delay full
early NMHC credits as permitted under
implementation past the last year of the schedule, and in each succeeding year
§ 86.1864–10(o)(5), the manufacturer
during the phase-in, the intended phaseprimary phase-in schedule (2013 for
must achieve a fleet average standard
in percentages for that model year and
LDV/LLDTs, 2015 for HLDT/MDPVs).
below 0.3 grams per mile for LDV/
An alternative phase-in schedule will be the remaining phase-in years along with
LLDTs and below 0.5 grams per mile for acceptable if it satisfies the following
the intended final sum of those
HLDT/MDPVs. Manufacturers must
percentages as described in paragraph
equations:
determine compliance with the cold
(g)(4)(i) of this section. This information
LDV/LLDTs:
temperature NMHC fleet average
may be included with the information
(6×API2008) + (5×API2009) + (4×API2010) + required under § 86.1844–01(d)(13). In
standard according to § 86.1864–10(o).
(3×API2011) + (2×API2012) + (1×API2013) its year end annual reports, as required
(3) Phase-in of the cold temperature
≥500%
NMHC standards. Except as permitted
under § 86.1844–01(e)(4), the
in § 86.1811–04(k)(5)(vi) and (vii)
HLDT/MDPVs:
manufacturer must include sufficient
regarding small volume manufacturers,
(6×API2010) + (5×API2011) + (4×API2012) + information so that the Administrator
manufacturers must comply with the
(3×API2013) + (2×API2014) + (1×API2015) can verify compliance with the
phase-in requirements in Tables S10–2
alternative phase-in schedule
≥500%
and S10–3 of this paragraph. Separate
established under paragraph (g)(4)(i) of
Where:
phase-in schedules are provided for
this section.
API = anticipated phase-in percentage
LDV/LLDTs and for HLDT/MDPVs.
(6)(i) Sales percentages for the
for the referenced model year
These requirements specify the
purpose of determining compliance
(ii) If the sum of products is greater
minimum percentage of the
with the phase-in of the cold
than or equal to 500%, which is the sum temperature NMHC requirements must
manufacturer’s LDV/LLDT and HLDT/
of products from the primary phase-in
MDPV 50-State sales, by model year,
be based upon projected 50-State sales
schedule (4 × 25% + 3 × 50% + 2 × 75% of LDV/LLDTs and HLDT/MDPVs of the
that must meet the fleet average cold
+ 1 × 100% = 500%), then the
temperature NMHC standard for their
applicable model year by the
alternative phase-in schedule is
full useful lives. LDVs and LLDTs must
manufacturer to the point of first sale.
acceptable, except as prohibited in
be grouped together to determine
Such sales percentages must be rounded
paragraphs (g)(4)(i) and (iii) of this
compliance with these phase-in
to the nearest one tenth of a percent.
section. In addition, manufacturers
requirements, and HLDTs and MDPVs
(ii) Alternatively, the manufacturer
electing to use an alternate phase-in
must also be grouped together to
may petition the Administrator to allow
determine compliance with these phase- schedule for compliance with the cold
actual volume produced for U.S. sales to
in requirements. Tables S10–2 and S10– temperature NMHC exhaust emission
be used in lieu of projected U.S. sales
standards must ensure that the sum of
3 follow:
for purposes of determining compliance
Percentage of
LDV/LLDTs
that must meet
requirement
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with the phase-in percentage
requirements under this section. The
manufacturer must submit its petition
within 30 days of the end of the model
year to the Compliance and Innovative
Strategies Division. For EPA to approve
the use of actual volume produced for
U.S. sales, the manufacturer must
establish to the satisfaction of the
Administrator, that actual production
volume is functionally equivalent to
actual sales volume of LDV/LLDTs and
HLDT/MDPVs sold in all 50 U.S. States.
(f) through (s) [Reserved]. For
guidance see § 86.1811–04.
(t) [Reserved]. For guidance see
§ 86.1811–09.
(u) Cold temperature NMHC exhaust
emission in-use standards for applicable
phase-in models. An interim full useful
life in-use compliance standard is
calculated by adding 0.1 g/mi to the FEL
to which each test group is newly
certified, and applies to that test group
only for the model years shown in
Tables S10–4 and S10–5. Otherwise, the
in-use standard is the certification
standard from paragraph (g)(2) of this
section. The standards apply for
purposes of in-use testing only and does
not apply to certification or Selective
Enforcement Auditing. Tables S10–4
and S10–5 follow:
TABLE S10–4.—IN-USE STANDARD FOR APPLICABLE PHASE-IN LDV/LLDTS
Model year of introduction
2008
Models years that the interim in-use standard is available .............................................
2009
2008
2009
2010
2011
2009
2010
2011
2012
2010
2011
2010
2011
2012
2013
2011
2012
2013
2012
2013
2012
2013
2014
2013
2014
TABLE S10–5.—IN-USE STANDARDS FOR APPLICABLE PHASE-IN HLDT/MDPVS
Model year of introduction
2010
Models years that the interim in-use standard is available .............................................
21. Section 86.1823–01 is amended by
revising paragraph (a)(3)(i)(C) to read as
follows:
§ 86.1823–01 Durability demonstration
procedures for exhaust emissions.
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*
*
*
*
*
(a) * * *
(3) * * *
(i) * * *
(C) The DF calculated by these
procedures will be used for determining
compliance with FTP exhaust emission
standards, SFTP exhaust emission
standards, cold temperature NMHC
emission standards, and cold CO
emission standards. At the
manufacturer’s option and using
procedures approved by the
Administrator, a separate DF may be
calculated exclusively using cold CO
test data to determine compliance with
cold CO emission standards. Similarly,
at the manufacturer’s option and using
procedures approved by the
Administrator, a separate DF may be
calculated exclusively using cold
temperature NMHC test data to
determine compliance with cold
temperature NMHC emission standards.
For determining compliance with full
useful life cold NMHC emission
standards, the 68–86 degree F 120,000
mile full useful life NMOG DF may be
used. Also at the manufacturer’s option
and using procedures approved by the
Administrator, a separate DF may be
calculated exclusively using US06 and/
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2010
2011
2012
2013
or air conditioning (SC03) test data to
determine compliance with the SFTP
emission standards.
*
*
*
*
*
22. Section 86.1827–01 is amended by
revising paragraph (a)(5) to read as
follows:
§ 86.1827–01
Test group determination.
*
*
*
*
*
(a) * * *
(5) Subject to the same emission
standards (or FEL in the case of cold
temperature NMHC standards), except
that a manufacturer may request to
group vehicles into the same test group
as vehicles subject to more stringent
standards, so long as all the vehicles
within the test group are certified to the
most stringent standards applicable to
any vehicle within that test group.
Light-duty trucks which are subject to
the same emission standards as lightduty vehicles with the exception of the
light-duty truck idle CO standard and/
or total HC standard may be included in
the same test group.
*
*
*
*
*
23. A new § 86.1828–10 is added to
Subpart S to read as follows:
§ 86.1828–10
selection.
Emission data vehicle
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2012
2013
2014
2012
2012
2013
2014
2015
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2013
2013
2014
2015
2014
2015
2014
2015
2016
2015
2016
by specifying the corresponding
paragraph and the statement
‘‘[Reserved]. For guidance see
§ 86.1828–01.’’ Where a corresponding
paragraph of § 86.1828–01 is not
applicable, this is indicated by the
statement ‘‘[Reserved].’’
(a) through (f) [Reserved]. For
guidance see § 86.1828–01.
(g) Cold temperature NMHC testing.
For cold temperature NMHC exhaust
emission compliance for each durability
group, the vehicle expected to emit the
highest NMHC emissions at 20 degrees
F on candidate in-use vehicles shall be
selected from the test vehicles specified
in § 86.1828–01(a). When the expected
worst-case cold temperature NMHC
vehicle is also the expected worst-case
cold CO vehicle as selected in paragraph
(c) of this section, then cold testing is
required only for that vehicle;
otherwise, testing is required for both
the worst-case cold CO vehicle and the
worst-case cold temperature NMHC
vehicle.
24. Section 86.1829–01 is amended by
revising paragraph (b)(3) to read as
follows:
§ 86.1829–01 Durability and emission
testing requirements; waivers.
*
Section 86.1828–10 includes text that
specifies requirements that differ from
§ 86.1828–01. Where a paragraph in
§ 86.1828–01 is identical and applicable
to § 86.1828–10, this may be indicated
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*
*
*
*
(b) * * *
(3) Cold temperature CO and cold
temperature NMHC Testing. One EDV in
each durability group shall be tested for
cold temperature CO and cold
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temperature NMHC exhaust emission
compliance in accordance with the test
procedures in subpart C of this part or
with alternative procedures requested
by the manufacturer and approved in
advance by the Administrator. The
selection of which EDV and test group
within the durability group will be
tested for cold temperature CO and cold
temperature NMHC compliance will be
determined under the provisions of
§ 86.1828–10(c) and (g).
*
*
*
*
*
25. Section 86.1844–01 is amended by
revising paragraph (d)(11) to read as
follows:
§ 86.1844–01 Information requirements:
Application for certification and submittal of
information upon request.
*
*
*
*
*
(d) * * *
(11) A list of all auxiliary emission
control devices (AECD) installed on any
applicable vehicles, including a
justification for each AECD, the
parameters they sense and control, a
detailed justification of each AECD
which results in a reduction in
effectiveness of the emission control
system, and rationale for why the AECD
is not a defeat device as defined under
§§ 86.1809–01 and 86.1809–10. For any
AECD uniquely used at high altitudes,
EPA may request engineering emission
data to quantify any emission impact
and validity of the AECD. For any AECD
uniquely used on multi-fuel vehicles
when operated on fuels other than
gasoline, EPA may request engineering
emission data to quantify any emission
impact and validity of the AECD.
*
*
*
*
*
26. A new § 86.1848–10 is added to
Subpart S to read as follows:
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§ 86.1848–10
Certification.
Section 86.1848–10 includes text that
specifies requirements that differ from
§ 86.1848–01. Where a paragraph in
§ 86.1848–01 is identical and applicable
to § 86.1848–10, this may be indicated
by specifying the corresponding
paragraph and the statement
‘‘[Reserved]. For guidance see
§ 86.1848–01.’’ Where a corresponding
paragraph of § 86.1848–01 is not
applicable, this is indicated by the
statement ‘‘[Reserved].’’
(a) through (b) [Reserved]. For
guidance see § 86.1848–01.
(c) All certificates are conditional
upon the following conditions being
met:
(1) The manufacturer must supply all
required information according to the
provisions of §§ 86.1843–01 and
86.1844–01.
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(2) The manufacturer must comply
with all certification and in-use
emission standards contained in
subparts S and H of this part both
during and after model year production.
(3) The manufacturer must comply
with all implementation schedules sales
percentages as required in § 86.1810 or
elsewhere in this part. Failure to meet
a required implementation schedule
sales percentage will be considered to
be a failure to satisfy a condition upon
which the certificate was issued and any
vehicles or trucks sold in violation of
the implementation schedule shall not
be covered by the certificate.
(4) For incomplete light-duty trucks
and incomplete heavy-duty vehicles, a
certificate covers only those new motor
vehicles which, when completed by
having the primary load-carrying device
or container attached, conform to the
maximum curb weight and frontal area
limitations described in the application
for certification as required in
§ 86.1844–01.
(5) The manufacturer must meet the
in-use testing and reporting
requirements contained in §§ 86.1845–
01, 86.1846–01, and 86.1847–01, as
applicable. Failure to meet the in-use
testing or reporting requirements shall
be considered a failure to satisfy a
condition upon which the certificate
was issued. A vehicle or truck will be
considered to be covered by the
certificate only if the manufacturer
fulfills this condition upon which the
certificate was issued.
(6) Vehicles are covered by a
certificate of conformity only if they are
in all material respects as described in
the manufacturer’s application for
certification (Part I and Part II).
(7) For Tier 2 and interim non-Tier 2
vehicles, all certificates of conformity
issued are conditional upon compliance
with all provisions of §§ 86.1811–04,
86.1860–04, 86.1861–04 and 86.1862–04
both during and after model year
production.
(i) Failure to meet the fleet average
NOX requirements of 0.07g/mi, 0.30 g/
mi or 0.20 g/mi, as applicable, will be
considered to be a failure to satisfy the
terms and conditions upon which the
certificate(s) was (were) issued and the
vehicles sold in violation of the fleet
average NOX standard will not be
covered by the certificate(s).
(ii) Failure to comply fully with the
prohibition against selling credits that it
has not generated or that are not
available, as specified in § 86.1861–04,
will be considered to be a failure to
satisfy the terms and conditions upon
which the certificate(s) was (were)
issued and the vehicles sold in violation
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of this prohibition will not be covered
by the certificate(s).
(iii) Failure to comply fully with the
phase-in requirements of § 86.1811–04,
will be considered to be a failure to
satisfy the terms and conditions upon
which the certificate(s) was (were)
issued and the vehicles sold which do
not comply with Tier 2 or interim nonTier 2 requirements, up to the number
needed to comply, will not be covered
by the certificate(s).
(iv) For paragraphs (c)(7)(i) through
(iii) of this section:
(A) The manufacturer must bear the
burden of establishing to the satisfaction
of the Administrator that the terms and
conditions upon which the certificate(s)
was (were) issued were satisfied.
(B) For recall and warranty purposes,
vehicles not covered by a certificate of
conformity will continue to be held to
the standards stated or referenced in the
certificate that otherwise would have
applied to the vehicles.
(8) For LDV/LLDTs and HLDT/
MDPVs, all certificates of conformity
issued are conditional upon compliance
with all provisions of §§ 86.1811–10 and
86.1864–10 both during and after model
year production.
(i) Failure to meet the fleet average
cold temperature NMHC requirements
will be considered a failure to satisfy the
terms and conditions upon which the
certificate(s) was (were) issued and the
vehicles sold in violation of the fleet
average NMHC standard will not be
covered by the certificate(s).
(ii) Failure to comply fully with the
prohibition against selling credits that
are not generated or that are not
available, as specified in § 86.1864–10,
will be considered a failure to satisfy the
terms and conditions upon which the
certificate(s) was (were) issued and the
vehicles sold in violation of this
prohibition will not be covered by the
certificate(s).
(iii) Failure to comply fully with the
phase-in requirements of § 86.1811–10
will be considered a failure to satisfy the
terms and conditions upon which the
certificate(s) was (were) issued and the
vehicles sold that do not comply with
cold temperature NMHC requirements,
up to the number needed to comply,
will not be covered by the certificate(s).
(iv) For paragraphs (c)(8)(i) through
(iii) of this section:
(A) The manufacturer bears the
burden of establishing to the satisfaction
of the Administrator that the terms and
conditions upon which the certificate(s)
was (were) issued were satisfied.
(B) For recall and warranty purposes,
vehicles not covered by a certificate of
conformity will continue to be held to
the standards stated or referenced in the
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certificate that otherwise would have
applied to the vehicles.
(d) through (i) [Reserved]. For
guidance see § 86.1848–01.
27. A new § 86.1864–10 is added to
Subpart S to read as follows:
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§ 86.1864–10 How to comply with the fleet
average cold temperature NMHC standards.
(a) Applicability. Cold temperature
NMHC exhaust emission standards
apply to the following vehicles, subject
to the phase-in requirements in
§ 86.1811–10(g)(3) and (4):
(1) 2010 and later model year LDV/
LLDTs.
(2) 2012 and later model year HLDT/
MDPVs.
(3) Aftermarket conversion systems as
defined in 40 CFR 85.502, including
conversion of MDPVs.
(4) Vehicles imported by ICIs as
defined in 40 CFR 85.1502.
(b) Useful life requirements. Full
useful life requirements for cold
temperature NMHC standards are
defined in § 86.1805–04(g). There is not
an intermediate useful life standard for
cold temperature NMHC standards.
(c) Altitude. Altitude requirements for
cold temperature NMHC standards are
provided in § 86.1810–09(f).
(d) Small volume manufacturer
certification procedures. Certification
procedures for small volume
manufacturers are provided in
§ 86.1838–01.
(e) Cold temperature NMHC
standards. Fleet average cold
temperature NMHC standards are
provided in § 86.1811–10(g)(2).
(f) Phase-in. Phase-in of the cold
temperature NMHC standards are
provided in § 86.1811–10(g)(3) and (4).
(g) Phase-in flexibilities for small
volume manufacturers. Phase-in
flexibilities for small volume
manufacturer compliance with the cold
temperature NMHC standards are
provided in § 86.1811–04(k)(5).
(h) Hardship provisions for small
volume manufacturers. Hardship
provisions for small volume
manufacturers related to the cold
temperature NMHC standards are
provided in § 86.1811–04(q)(1).
(i) In-use standards for applicable
phase-in models. In-use cold
temperature NMHC standards for
applicable phase-in models are
provided in § 86.1811–10(u).
(j) Durability procedures and method
of determining deterioration factors
(DFs). The durability data vehicle
selection procedures of § 86.1822–01
and the durability demonstration
procedures of § 86.1823–06 apply for
cold NMHC standards. For determining
compliance with full useful life cold
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temperature NMHC emission standards,
the 68–86 degree F, 120,000 mile full
useful life NMOG DF may be used.
(k) Vehicle test procedure. (1) The test
procedure for demonstrating
compliance with cold temperature
NMHC standards is contained in
subpart C of this part. With prior EPA
approval, alternative testing procedures
may be used, as specified in § 86.106–
96(a), provided cold temperature NMHC
emissions do not decrease as a result of
an alternative testing procedure.
(2) Testing of all LDVs, LDTs and
MDPVs to determine compliance with
cold temperature NMHC exhaust
emission standards set forth in this
section must be on a loaded vehicle
weight (LVW) basis, as defined in
§ 86.1803–01.
(3) Testing for the purpose of
providing certification data is required
only at low altitude conditions and only
for vehicles that can operate on
gasoline, except as requested in
§§ 86.1810–09(f) and 86.1844–01(d)(11).
If hardware and software emission
control strategies used during low
altitude condition testing are not used
similarly in-use across all altitudes, the
manufacturer will include a statement
in the application for certification, in
accordance with §§ 86.1844–01(d)(11)
and § 86.1810–09(f), stating what the
different strategies are and why they are
used. If hardware and software emission
control strategies used during testing
with gasoline are not used similarly
with all fuels that can be used in multifuel vehicles, the manufacturer will
include a statement in the application
for certification, in accordance with
§§ 86.1844–01(d)(11) and 86.1810–09(f),
stating what the different strategies are
and why they are used. For example,
unless a manufacturer states otherwise,
air pumps used to control emissions on
dedicated gasoline vehicles or multifuel vehicles during low altitude
conditions must also be used to control
emissions at high altitude conditions,
and software used to control emissions
or closed loop operation must also
operate similarly at low and high
altitude conditions and similarly when
multi-fueled vehicles are operated on
gasoline and alternate fuels. These
examples are for illustrative purposes
only; similar strategies would apply to
other currently used emission control
technologies and/or emerging or future
technologies.
(l) Emission data vehicle (EDV)
selection. Provisions for selecting the
appropriate EDV for the cold
temperature NMHC standards are
provided in §§ 86.1828–10(g) and
86.1829–01(b)(3).
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(m) Calculating the fleet average cold
temperature NMHC standard.
Manufacturers will compute separate
sales-weighted fleet average cold
temperature NMHC emissions at the end
of the model year for LDV/LLDTs and
HLDT/MDPVs, using actual sales, and
certifying test groups to FELs, as defined
in § 86.1803–01. The FEL becomes the
standard for each test group, and every
test group can have a different FEL. The
certification resolution for the FEL will
be one decimal point. LDVs and LLDTs
must be grouped together when
calculating the fleet average, and HLDTs
and MDPVs must also be grouped
together to determine the fleet average.
Manufacturers must compute the salesweighted cold temperature NMHC fleet
averages using the following equation,
rounded to the nearest tenth:
Fleet average cold temperature NMHC
exhaust emissions =
S(N × FEL) ÷ Total number of vehicles
sold of the applicable weight category
(i.e., either LDV + LLDTs, or HLDT +
MDPVs)
Where:
N = The number of LDVs and LLDTs, or
HLDTs and MDPVs, sold within the
applicable FEL, based on vehicles
counted to the point of first sale.
FEL = Family Emission Limit.
(n) Certification compliance and
enforcement requirements for cold
temperature NMHC standards. (1) In
addition to the compliance and
enforcement requirements provided
throughout § 86.1864–10, additional
conditions are included in the
provisions of § 86.1848–10(c)(8).
(2) The certificate issued for each test
group requires all vehicles within that
test group to meet the emission standard
or FEL to which the vehicles were
certified.
(3) Each manufacturer must comply
with the applicable cold temperature
NMHC fleet average standard on a salesweighted average basis, at the end of
each model year, using the procedure
described in paragraph (m) of this
section.
(4) During a phase-in year, the
manufacturer must comply with the
applicable cold temperature NMHC fleet
average standard for the required phasein percentage for that year as specified
in § 86.1811–10(g)(3) or (4).
(5) Manufacturers must compute
separate cold temperature NMHC fleet
averages for LDV/LLDTs and HLDT/
MDPVs. The sales-weighted cold
temperature NMHC fleet averages must
be compared with the applicable fleet
average standard.
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(6) Each manufacturer must comply
on an annual basis with the fleet average
standards as follows:
(i) Manufacturers must report in their
annual reports to the Agency that they
met the relevant corporate average
standard by showing that their salesweighted average cold temperature
NMHC emissions of LDV/LLDTs and
HLDT/MDPVs, as applicable, are at or
below the applicable fleet average
standard;
(ii) If the sales-weighted average is
above the applicable fleet average
standard, manufacturers must obtain
and apply sufficient NMHC credits, as
appropriate, and as permitted under
paragraph (o)(8) of this section. A
manufacturer must show via the use of
credits that they have offset any
exceedence of the corporate average
standard. Manufacturers shall also
report their credit balances or deficits.
(iii) If a manufacturer fails to meet the
corporate average cold temperature
NMHC standard for two consecutive
years, as required in paragraph (o)(8) of
this section, the vehicles causing the
corporate average exceedence will be
considered not covered by the certificate
of conformity. A manufacturer will be
subject to penalties on an individualvehicle basis for sale of vehicles not
covered by a certificate.
(iv) EPA will review each
manufacturer’s sales to designate the
vehicles that caused the exceedence of
the corporate average standard. EPA
will designate as nonconforming those
vehicles in test groups with the highest
certification emission values first,
continuing until a number of vehicles
equal to the calculated number of
noncomplying vehicles as determined
above is reached. In a group where only
a portion of vehicles would be deemed
nonconforming, EPA will determine the
actual nonconforming vehicles by
counting backwards from the last
vehicle produced in that test group.
Manufacturers will be liable for
penalties for each vehicle sold that is
not covered by a certificate.
(o) How does the cold temperature
NMHC averaging, banking and trading
(ABT) program work? (1) Manufacturers
shall average the cold temperature
NMHC emissions of their vehicles and
comply with the cold temperature
NMHC fleet average corporate standard.
Credits may be generated during and
after the phase-in period. Credits may
also be generated prior to the phase-in
periods as described in paragraph (5) of
this section. A manufacturer whose cold
temperature NMHC fleet average
emissions exceed the 0.3 g/mile
standard for LDV/LLDTs, or 0.5 g/mi for
HLDT/MDPVs, must complete the
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calculation in paragraph (o)(4) of this
section to determine the size of its
NMHC credit deficit. A manufacturer
whose cold temperature NMHC fleet
average emissions are less than the 0.3
g/mile standard for LDV/LLDTs, or less
than 0.5 g/mi for HLDT/MDPVs, must
complete the calculation in paragraph
(o)(4) of this section if it desires to
generate NMHC credits.
(2) There are no property rights
associated with NMHC credits generated
under this subpart. Credits are a limited
authorization to emit the designated
amount of emissions. Nothing in this
part or any other provision of law
should be construed to limit EPA’s
authority to terminate or limit this
authorization through a rulemaking.
(3) Each manufacturer must comply
with the reporting and recordkeeping
requirements of paragraph (p) of this
section for NMHC credits, including
early credits. The averaging, banking
and trading program shall be enforced
through the certificate of conformity
that allows the manufacturer to
introduce any regulated vehicles into
commerce.
(4) Credits are earned on the last day
of the model year. Manufacturers must
calculate, for a given model year, the
number of credits or debits it has
generated according to the following
equation, rounded to the nearest tenth:
NMHC Credits or Debits = (Cold
Temperature NMHC
Standard¥Manufacturer’s SalesWeighted Fleet Average Cold
Temperature NMHC Emissions) ×
(Total Number of Vehicles Sold)
Where:
Cold Temperature NMHC Standard =
0.3 g/mi for LDV/LLDTs or 0.5 g/mi
for HLDT/MDPV, per § 86.1811–
10(g)(2).
Manufacturer’s Sales-Weighted Fleet
Average Cold Temperature NMHC
Emissions = average calculated
according to paragraph (m) of this
section.
Total Number of Vehicles Sold = Total
50-State sales based on the point of
first sale.
(5) The following provisions apply for
early banking:
(i) Manufacturers may certify LDV/
LLDTs to the cold temperature NMHC
exhaust standards in § 86.1811–10(g)(2)
for model years 2008–2009 in order to
bank credits for use in the 2010 and
later model years. Manufacturers may
certify HLDT/MDPVs to the cold
temperature NMHC exhaust standards
in § 86.1811–10(g)(2) for model years
2010–2011 in order to bank credits for
use in the 2012 and later model years.
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(ii) This process is referred to as
‘‘early banking’’ and the resultant
credits are referred to as ‘‘early credits.’’
In order to bank early credits, a
manufacturer must comply with all
exhaust emission standards and
requirements applicable to LDV/LLDTs
and/or HLDT/MDPVs. To generate early
credits, a manufacturer must separately
compute the sales-weighted cold
temperature NMHC average of the LDV/
LLDTs and HLDT/MDPVs it certifies to
the exhaust requirements and separately
compute credits using the calculations
in paragraph (o)(4) of this section. Early
HLDT/MDPV credits may not be applied
to LDV/LLDTs before the 2010 model
year. Early LDV/LLDT credits may not
be applied to HLDT/ MDPV before the
2012 model year.
(6) NMHC credits are not subject to
any discount or expiration date except
as required under the deficit
carryforward provisions of paragraph
(o)(8) of this section. There shall be no
discounting of unused credits. NMHC
credits shall have unlimited lives,
subject to the limitations of paragraph
(o)(2) of this section.
(7) Credits may be used as follows:
(i) Credits generated and calculated
according to the method in paragraph
(o)(4) of this section may only be used
to offset deficits accrued with respect to
the standard in § 86.1811–10(g)(2).
Credits may be banked and used in a
future model year in which a
manufacturer’s average cold
temperature NMHC level exceeds the
0.3 or 0.5 g/mi standard for LDV/LLDTs
and HLDT/MDPVs, respectively. Credits
may be exchanged between the LDT/
LLDT and HLDT/MDPV fleets of a given
manufacturer. Credits may also be
traded to another manufacturer
according to the provisions in paragraph
(o)(9) of this section. Before trading or
carrying over credits to the next model
year, a manufacturer must apply
available credits to offset any credit
deficit, where the deadline to offset that
credit deficit has not yet passed.
(ii) The use of credits shall not be
permitted to address Selective
Enforcement Auditing or in-use testing
failures. The enforcement of the
averaging standard shall occur through
the vehicle’s certificate of conformity. A
manufacturer’s certificate of conformity
shall be conditioned upon compliance
with the averaging provisions. The
certificate shall be void ab initio if a
manufacturer fails to meet the corporate
average standard and does not obtain
appropriate credits to cover its shortfalls
in that model year or in the subsequent
model year (see deficit carryforward
provision in paragraph (o)(8) of this
section). Manufacturers shall track their
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certification levels and sales unless they
produce only vehicles certified to cold
temperature NMHC levels below the
standard and do not plan to bank
credits.
(8) The following provisions apply if
debits are accrued:
(i) If a manufacturer calculates that it
has negative credits (also called
‘‘debits’’ or a ‘‘credit deficit’’) for a given
model year, it shall be allowed to carry
that deficit forward into the next model
year. Such a carry-forward may only
occur after the manufacturer exhausts
any supply of banked credits. At the end
of that next model year, the deficit must
be covered with an appropriate number
of credits that the manufacturer
generates or purchases. Any remaining
deficit shall be subject to an
enforcement action, as described in this
paragraph (o)(8). Manufacturers are not
permitted to run a deficit for two
consecutive years.
(ii) If debits are not offset within the
specified time period, the number of
vehicles not meeting the fleet average
cold temperature NMHC standards and
not covered by the certificate must be
calculated by dividing the total amount
of debits for the model year by the fleet
average cold temperature NMHC
standard applicable for the model year
in which the debits were first incurred.
(iii) EPA will determine the number
of vehicles for which the condition on
the certificate was not satisfied by
designating vehicles in those test groups
with the highest certification cold
temperature NMHC emission values
first and continuing until a number of
vehicles equal to the calculated number
of noncomplying vehicles as determined
above is reached. If this calculation
determines that only a portion of
vehicles in a test group contribute to the
debit situation, then EPA will designate
actual vehicles in that test group as not
covered by the certificate, starting with
the last vehicle produced and counting
backwards.
(iv)(A) If a manufacturer ceases
production of LDV/LLDTs and HLDT/
MDPVs, the manufacturer continues to
be responsible for offsetting any debits
outstanding within the required time
period. Any failure to offset the debits
will be considered a violation of
paragraph (o)(8)(i) of this section and
may subject the manufacturer to an
enforcement action for sale of vehicles
not covered by a certificate, pursuant to
paragraphs (o)(8)(ii) and (iii) of this
section.
(B) If a manufacturer is purchased by,
merges with, or otherwise combines
with another manufacturer, the
controlling entity is responsible for
offsetting any debits outstanding within
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16:05 Mar 28, 2006
Jkt 208001
the required time period. Any failure to
offset the debits will be considered a
violation of paragraph (o)(8)(i) of this
section and may subject the
manufacturer to an enforcement action
for sale of vehicles not covered by a
certificate, pursuant to paragraphs
(o)(8)(ii) and (iii) of this section.
(v) For purposes of calculating the
statute of limitations, a violation of the
requirements of paragraph (o)(8)(i) of
this section, a failure to satisfy the
conditions upon which a certificate(s)
was issued and hence a sale of vehicles
not covered by the certificate, all occur
upon the expiration of the deadline for
offsetting debits specified in paragraph
(o)(8)(i) of this section.
(9) The following provisions apply to
NMHC credit trading:
(i) EPA may reject NMHC credit
trades if the involved manufacturers fail
to submit the credit trade notification in
the annual report. A manufacturer may
not sell credits that are not available for
sale pursuant to the provisions in
paragraphs (o)(7)(i) of this section.
(ii) In the event of a negative credit
balance resulting from a transaction that
a manufacturer could not cover by the
reporting deadline for the model year in
which the trade occurred, both the
buyer and seller are liable, except in
cases involving fraud. EPA may void ab
initio the certificates of conformity of all
engine families participating in such a
trade.
(iii) A manufacturer may only trade
credits that it has generated pursuant to
paragraph (o)(4) of this section or
acquired from another party.
(p) Maintenance of records and
submittal of information relevant to
compliance with fleet average cold
temperature NMHC standards—(1)
Maintenance of records. (i)
Manufacturers producing any light-duty
vehicles, light-duty trucks, or mediumduty passenger vehicles subject to the
provisions in this subpart must
establish, maintain, and retain all the
following information in adequately
organized and indexed records for each
model year:
(A) Model year.
(B) Applicable fleet average cold
temperature NMHC standard: 0.3g/mi
for LDV/LLDTs; 0.5 g/mi for HLDT/
MDPVs.
(C) Fleet average cold temperature
NMHC value achieved.
(D) All values used in calculating the
fleet average cold temperature NMHC
value achieved.
(ii) Manufacturers producing any
light-duty vehicles, light-duty trucks, or
medium-duty passenger vehicles subject
to the provisions in this subpart must
establish, maintain, and retain all the
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following information in adequately
organized and indexed records for each
LDV/T or MDPV subject to this subpart:
(A) Model year.
(B) Applicable fleet average cold
temperature NMHC standard.
(C) EPA test group.
(D) Assembly plant.
(E) Vehicle identification number.
(F) Cold temperature NMHC FEL to
which the LDV/T or MDPV is certified.
(G) Information on the point of first
sale, including the purchaser, city, and
state.
(iii) Manufacturers must retain all
records required to be maintained under
this section for a period of eight years
from the due date for the annual report.
Records may be stored in any format
and on any media, as long as
manufacturers can promptly send EPA
organized, written records in English if
we ask for them. Manufacturers must
keep records readily available as EPA
may review them at any time.
(iv) Nothing in this section limits the
Administrator’s discretion to require the
manufacturer to retain additional
records or submit information not
specifically required by this section.
(v) Pursuant to a request made by the
Administrator, the manufacturer must
submit to the Administrator the
information that the manufacturer is
required to retain.
(vi) EPA may void ab initio a
certificate of conformity for vehicles
certified to emission standards as set
forth or otherwise referenced in this
subpart for which the manufacturer fails
to retain the records required in this
section or to provide such information
to the Administrator upon request.
(2) Reporting. (i) Each covered
manufacturer must submit an annual
report. The annual report must contain
for each applicable cold temperature
NMHC standard, the fleet average cold
temperature NMHC value achieved, all
values required to calculate the cold
temperature NMHC emissions value, the
number of credits generated or debits
incurred, all the values required to
calculate the credits or debits, the
resulting balance of credits or debits,
and sufficient information to show
compliance with all phase-in or
alternative phase-in requirements.
(ii) For each applicable fleet average
cold temperature NMHC standard, the
annual report must also include
documentation on all credit transactions
the manufacturer has engaged in since
those included in the last report.
Information for each transaction must
include all of the following:
(A) Name of credit provider.
(B) Name of credit recipient.
(C) Date the trade occurred.
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(D) Quantity of credits traded.
(E) Model year in which the credits
were earned.
(iii) Unless a manufacturer reports the
data required by this section in the
annual production report required
under § 86.1844–01(e), a manufacturer
must submit an annual report for each
model year after production ends for all
affected vehicles produced by the
manufacturer subject to the provisions
of this subpart and no later than May 1
of the calendar year following the given
model year. Annual reports must be
submitted to: Director, Compliance and
Innovative Strategies Division, U.S.
Environmental Protection Agency, 2000
VerDate Aug<31>2005
16:05 Mar 28, 2006
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48105.
(iv) Failure by a manufacturer to
submit the annual report in the
specified time period for all vehicles
subject to the provisions in this section
is a violation of section 203(a)(1) of the
Clean Air Act (42 U.S.C. 7522) for each
applicable vehicle produced by that
manufacturer.
(v) If EPA or the manufacturer
determines that a reporting error
occurred on an annual report previously
submitted to EPA, the manufacturer’s
credit or debit calculations will be
recalculated. EPA may void erroneous
credits, unless traded, and must adjust
erroneous debits. In the case of traded
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15963
erroneous credits, EPA must adjust the
selling manufacturer’s credit or debit
balance to reflect the sale of such credits
and any resulting generation of debits.
(3) Notice of opportunity for hearing.
Any voiding of the certificate under
paragraph (p)(1)(vi) of this section will
be made only after EPA has offered the
affected manufacturer an opportunity
for a hearing conducted in accordance
with § 86.614–84 for light-duty vehicles
or § 86.1014–84 for light-duty trucks
and, if a manufacturer requests such a
hearing, will be made only after an
initial decision by the Presiding Officer.
[FR Doc. 06–2315 Filed 3–28–06; 8:45 am]
BILLING CODE 6560–50–P
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Agencies
[Federal Register Volume 71, Number 60 (Wednesday, March 29, 2006)]
[Proposed Rules]
[Pages 15804-15963]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-2315]
[[Page 15803]]
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Part II
Environmental Protection Agency
-----------------------------------------------------------------------
40 CFR Parts 59, 80, 85 and 86
Control of Hazardous Air Pollutants From Mobile Sources; Proposed Rule
Federal Register / Vol. 71, No. 60 / Wednesday, March 29, 2006 /
Proposed Rules
[[Page 15804]]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Parts 59, 80, 85 and 86
[EPA-HQ-OAR-2005-0036; FRL-8041-2]
RIN 2060-AK70
Control of Hazardous Air Pollutants From Mobile Sources
AGENCY: Environmental Protection Agency (EPA).
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: Today EPA is proposing controls on gasoline, passenger
vehicles, and portable gasoline containers (gas cans) that would
significantly reduce emissions of benzene and other hazardous air
pollutants (``mobile source air toxics''). Benzene is a known human
carcinogen, and mobile sources are responsible for the majority of
benzene emissions. The other mobile source air toxics are known or
suspected to cause cancer or other serious health effects.
We are proposing to limit the benzene content of gasoline to an
annual average of 0.62% by volume, beginning in 2011. We are also
proposing to limit exhaust emissions of hydrocarbons from passenger
vehicles when they are operated at cold temperatures. This standard
would be phased in from 2010 to 2015. For passenger vehicles we also
propose evaporative emissions standards that are equivalent to those in
California. Finally, we are proposing a hydrocarbon emissions standard
for gas cans beginning in 2009, which would reduce evaporation and
spillage of gasoline from these containers.
These controls would significantly reduce emissions of benzene and
other mobile source air toxics such as 1,3-butadiene, formaldehyde,
acetaldehyde, acrolein, and naphthalene. This proposal would result in
additional substantial benefits to public health and welfare by
significantly reducing emissions of particulate matter from passenger
vehicles.
We project annual nationwide benzene reductions of 35,000 tons in
2015, increasing to 65,000 tons by 2030. Total reductions in mobile
source air toxics would be 147,000 tons in 2015 and over 350,000 tons
in 2030. Passenger vehicles in 2030 would emit 45% less benzene. Gas
cans meeting the new standards would emit almost 80% less benzene.
Gasoline would have 37% less benzene overall. We estimate that these
reductions would have an average cost of less than 1 cent per gallon of
gasoline and less than $1 per vehicle. The average cost for gas cans
would be less than $2 per can. The reduced evaporation from gas cans
would result in significant fuel savings, which would more than offset
the increased cost for the gas can.
DATES: Comments must be received on or before May 30, 2006. Under the
Paperwork Reduction Act, comments on the information collection
provisions must be received by OMB on or before April 28, 2006.
Hearing: We will hold a public hearing on April 12, 2006. The
hearing will start at 10 a.m. local time and continue until everyone
has had a chance to speak. If you want to testify at the hearing,
notify the contact person listed under FOR FURTHER INFORMATION CONTACT
by April 3, 2006.
ADDRESSES: Submit your comments, identified by Docket ID No. EPA-HQ-
OAR-2005-0036, by one of the following methods:
https://www.regulations.gov: Follow the on-line
instructions for submitting comments.
Fax your comments to: (202) 566-1741.
Mail: Air Docket, Environmental Protection Agency,
Mailcode: 6102T, 1200 Pennsylvania Ave., NW., Washington, DC 20460. In
addition, please mail a copy of your comments on the information
collection provisions to the Office of Information and Regulatory
Affairs, Office of Management and Budget (OMB), Attn: Desk Officer for
EPA, 725 17th St. NW., Washington, DC 20503.
Hand Delivery: EPA Docket Center, (EPA/DC) EPA West, Room
B102, 1301 Constitution Ave., NW., Washington, DC 20004. Such
deliveries are only accepted during the Docket's normal hours of
operation, and special arrangements should be made for deliveries of
boxed information.
Instructions: Direct your comments to Docket ID No. EPA-HQ-OAR-
2005-0036. EPA's policy is that all comments received will be included
in the public docket without change and may be made available online at
www.regulations.gov, including any personal information provided,
unless the comment includes information claimed to be Confidential
Business Information (CBI) or other information whose disclosure is
restricted by statute. Do not submit information that you consider to
be CBI or otherwise protected through www.regulations.gov or e-mail.
The www.regulations.gov website is an ``anonymous access'' system,
which means EPA will not know your identity or contact information
unless you provide it in the body of your comment. If you send an e-
mail comment directly to EPA without going through www.regulations.gov
your e-mail address will be automatically captured and included as part
of the comment that is placed in the public docket and made available
on the Internet. If you submit an electronic comment, EPA recommends
that you include your name and other contact information in the body of
your comment and with any disk or CD-ROM you submit. If EPA cannot read
your comment due to technical difficulties and cannot contact you for
clarification, EPA may not be able to consider your comment. Electronic
files should avoid the use of special characters, any form of
encryption, and be free of any defects or viruses. For additional
information about EPA's public docket visit the EPA Docket Center
homepage at https://www.epa.gov/epahome/dockets.htm. For additional
instructions on submitting comments, go to section XI, Public
Participation, of the SUPPLEMENTARY INFORMATION section of this
document.
Docket: All documents in the docket are listed in the
www.regulations.gov index. Although listed in the index, some
information is not publicly available, e.g., CBI or other information
whose disclosure is restricted by statute. Certain other material, such
as copyrighted material, will be publicly available only in hard copy.
Publicly available docket materials are available either electronically
in www.regulations.gov or in hard copy at the Air Docket, EPA/DC, EPA
West, Room B102, 1301 Constitution Ave., NW., Washington, DC. The
Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room is (202) 566-1744, and the telephone number for the Air
Docket is (202) 566-1742.
Hearing: The public hearing will be held at Sheraton Crystal City
Hotel, 1800 Jefferson Davis Highway, Arlington, Virginia 22202,
Telephone: (703) 486-1111. See section XI, Public Participation, for
more information about public hearings.
FOR FURTHER INFORMATION CONTACT: Mr. Chris Lieske, U.S. EPA, Office of
Transportation and Air Quality, Assessment and Standards Division
(ASD), Environmental Protection Agency, 2000 Traverwood Drive, Ann
Arbor, MI 48105; telephone number: (734) 214-4584; fax number: (734)
214-4816; email address: lieske.christopher@epa.gov, or Assessment and
Standards Division
[[Page 15805]]
Hotline; telephone number: (734) 214-4636; e-mail address:
asdinfo@epa.gov.
SUPPLEMENTARY INFORMATION:
General Information
A. Does this Action Apply to Me?
Entities potentially affected by this action are those that produce
new motor vehicles, alter individual imported motor vehicles to address
U.S. regulation, or convert motor vehicles to use alternative fuels. It
would also affect you if you produce gasoline motor fuel or manufacture
portable gasoline containers. Regulated categories include:
----------------------------------------------------------------------------------------------------------------
NAICS SIC codes
Category codes \a\ \b\ Examples of potentially affected entities
----------------------------------------------------------------------------------------------------------------
Industry...................... 336111 3711 Motor vehicle manufacturers.
Industry...................... 335312 3621 Alternative fuel vehicle converters.
424720 5172
811198 7539
........... 7549 ......................................................
Industry...................... 811111 7538 Independent commercial importers.
811112 7533 ......................................................
811198 7549 ......................................................
Industry...................... 324110 2911 Gasoline fuel refiners.
Industry...................... 326199 3089 Portable fuel container manufacturers.
332431 3411 ......................................................
----------------------------------------------------------------------------------------------------------------
\a\ North American Industry Classification System (NAICS).
\b\ Standard Industrial Classification (SIC) system code.
This table is not intended to be exhaustive, but rather provides a
guide for readers regarding entities likely to be regulated by this
action. This table lists the types of entities that EPA is now aware
could potentially be regulated by this action. Other types of entities
not listed in the table could also be regulated. To determine whether
your activities are regulated by this action, you should carefully
examine the applicability criteria in 40 CFR parts 59, 80, 85, and 86.
If you have any questions regarding the applicability of this action to
a particular entity, consult the person listed in the preceding FOR
FURTHER INFORMATION CONTACT section.
B. What Should I Consider as I Prepare My Comments for EPA?
1. Submitting CBI
Do not submit this information to EPA through www.regulations.gov
or e-mail. Clearly mark the part or all of the information that you
claim to be confidential business information (CBI). For CBI
information in a disk or CD ROM that you mail to EPA, mark the outside
of the disk or CD ROM as CBI and then identify electronically within
the disk or CD ROM the specific information that is claimed as CBI. In
addition to one complete version of the comment that includes
information claimed as CBI, a copy of the comment that does not contain
the information claimed as CBI must be submitted for inclusion in the
public docket. Information so marked will not be disclosed except in
accordance with procedures set forth in 40 CFR part 2.
2. Tips for Preparing Your Comments
When submitting comments, remember to:
Explain your views as clearly as possible.
Describe any assumptions that you used.
Provide any technical information and/or data you used
that support your views.
If you estimate potential burden or costs, explain how you
arrived at your estimate.
Provide specific examples to illustrate your concerns.
Offer alternatives.
Make sure to submit your comments by the comment period
deadline identified.
To ensure proper receipt by EPA, identify the appropriate
docket identification number in the subject line on the first page of
your response. It would also be helpful if you provided the name, date,
and Federal Register citation related to your comments.
Outline of This Preamble
I. Introduction
A. Summary
B. What Background Information is Helpful to Understand this
Proposal?
1. What Are Air Toxics and Related Health Effects?
2. What is the Statutory Authority for Today's Proposal?
a. Clean Air Act Section 202(l)
b. Clean Air Act Section 183(e)
c. Energy Policy Act
3. What Other Actions Has EPA Taken Under Clean Air Act Section
202(l)?
a. 2001 Mobile Source Air Toxics Rule
b. Technical Analysis Plan
II. Overview of Proposal
A. Why Is EPA Making This Proposal?
1. National Cancer Risk from Air Toxics
2. Noncancer Health Effects
3. Exposure Near Roads and From Attached Garages
4. Ozone and Particulate Matter
B. What Is EPA Proposing?
1. Light-Duty Vehicle Emission Standards
2. Gasoline Fuel Standards
3. Portable Gasoline Container (Gas Can) Controls
III. What Are Mobile Source Air Toxics (MSATs) and Their Health
Effects?
A. What Are MSATs?
B. Compounds Emitted by Mobile Sources and Identified in IRIS
C. Which Mobile Source Emissions Pose the Greatest Health Risk
at Current Levels?
1. National and Regional Risk Drivers in 1999 National-Scale Air
Toxics Assessment
2. 1999 NATA Risk Drivers with Significant Mobile Source
Contribution
D. What Are the Health Effects of Air Toxics?
1. Overview of Potential Cancer and Noncancer Health Effects
2. Health Effects of Key MSATs
a. Benzene
b. 1,3-Butadiene
c. Formaldehyde
d. Acetaldehyde
e. Acrolein
f. Polycyclic Organic Matter (POM)
g. Naphthalene
h. Diesel Particulate Matter and Diesel Exhaust Organic Gases
E. Gasoline PM
F. Near-Roadway Health Effects
G. How Would This Proposal Reduce Emissions of MSATs?
IV. What Are the Air Quality and Health Impacts of Air Toxics, and
How do Mobile Sources Contribute?
A. What Is the Health Risk to the U.S. Population from
Inhalation Exposure to Ambient Sources of Air Toxics, and How Would
It be Reduced by the Proposed Controls?
[[Page 15806]]
B. What is the Distribution of Exposure and Risk?
1. Distribution of National-Scale Estimates of Risk from Air
Toxics
2. Elevated Concentrations and Exposure in Mobile Source-
Impacted Areas
a. Concentrations Near Major Roadways
b. Exposures Near Major Roadways
i. Vehicles
ii. Homes and Schools
iii. Pedestrians and Bicyclists
c. Exposure and Concentrations in Homes with Attached Garages
d. Occupational Exposure
3. What Are the Size and Characteristics of Highly Exposed
Populations?
4. What Are the Implications for Distribution of Individual
Risk?
C. Ozone
1. Background
2. Health Effects of Ozone
3. Current and Projected 8-hour Ozone Levels
D. Particulate Matter
1. Background
2. Health Effects of PM
3. Current and Projected PM2.5 Levels
4. Current PM10 Levels
E. Other Environmental Effects
1. Visibility
a. Background
b. Current Visibility Impairment
c. Future Visibility Impairment
2. Plant Damage from Ozone
3. Atmospheric Deposition
4. Materials Damage and Soiling
V. What Are Mobile Source Emissions Over Time and How Would This
Proposal Reduce Emissions, Exposure and Associated Health Effects?
A. Mobile Source Contribution to Air Toxics Emissions
B. VOC Emissions from Mobile Sources
C. PM Emissions from Mobile Sources
D. Description of Current Mobile Source Emissions Control
Programs that Reduce MSATs
1. Fuels Programs
a. RFG
b. Anti-dumping
c. 2001 Mobile Source Air Toxics Rule (MSAT1)
d. Gasoline Sulfur
e. Gasoline Volatility
f. Diesel Fuel
g. Phase-Out of Lead in Gasoline
2. Highway Vehicle and Engine Programs
3. Nonroad Engine Programs
4. Voluntary Programs
E. Emission Reductions from Proposed Controls
1. Proposed Vehicle Controls
a. Volatile Organic Compounds (VOC)
b. Toxics
c. PM2.5
2. Proposed Fuel Benzene Controls
3. Proposed Gas Can Standards
a. VOC
b. Toxics
4. Total Emission Reductions from Proposed Controls
a. Toxics
b. VOC
c. PM2.5
F. How Would This Proposal Reduce Exposure to Mobile Source Air
Toxics and Associated Health Effects?
G. Additional Programs Under Development That Will Reduce MSATs
1. On-Board Diagnostics for Heavy-Duty Vehicles Over 14,000
Pounds
2. Standards for Small SI Engines
3. Standards for Locomotive and Marine Engines
VI. Proposed New Light-duty Vehicle Standards
A. Why are We Proposing New Standards?
1. The Clean Air Act and Air Quality
2. Technology Opportunities for Light-Duty Vehicles
3. Cold Temperature Effects on Emission Levels
a. How Does Temperature Affect Emissions?
b. What Are the Current Emissions Control Requirements?
c. Opportunities for Additional Control
B. What Cold Temperature Requirements Are We Proposing?
1. NMHC Exhaust Emissions Standards
2. Feasibility of the Proposed Standards
a. Currently Available Emission Control Technologies
b. Feasibility Considering Current Certification Levels,
Deterioration and Compliance Margin
c. Feasibility and Test Programs for Higher Weight Vehicles
3. Standards Timing and Phase-in
a. Phase-In Schedule
b. Alternative Phase-In Schedules
4. Certification Levels
5. Credit Program
a. How Credits Are Calculated
b. Credits Earned Prior to Primary Phase-In Schedule
c. How Credits Can Be Used
d. Discounting and Unlimited Life
e. Deficits Could Be Carried Forward
f. Voluntary Heavy-Duty Vehicle Credit Program
6. Additional Vehicle Cold Temperature Standard Provisions
a. Applicability
b. Useful Life
c. High Altitude
d. In-Use Standards for Vehicles Produced During Phase-in
7. Monitoring and Enforcement
C. What Evaporative Emissions Standards Are We Proposing?
1. Current Controls and Feasibility of the Proposed Standards
2. Evaporative Standards Timing
3. Timing for Multi-Fueled Vehicles
4. In-Use Evaporative Emission Standards
5. Existing Differences Between California and Federal
Evaporative Emission Test Procedures
D. Opportunities for Additional Exhaust Control Under Normal
Conditions
E. Vehicle Provisions for Small Volume Manufacturers
1. Lead Time Transition Provisions
2. Hardship Provisions
3. Special Provisions for Independent Commercial Importers
(ICIs)
VII. Proposed Gasoline Benzene Control Program
A. Overview of Today's Proposed Fuel Control Program
B. Description of the Proposed Fuel Control Program
C. Development of the Proposed Gasoline Benzene Standard
1. Why Are We Focusing on Controlling Benzene Emissions?
a. Other MSAT Emissions
b. MSAT Emission Reductions Through Lowering Gasoline Volatility
or Sulfur Content
i. Gasoline Sulfur Content
ii. Gasoline Vapor Pressure
c. Toxics Performance Standard
d. Diesel Fuel Changes
2. Why Are We Proposing To Control Benzene Emissions By
Controlling Gasoline Benzene Content?
a. Benzene Content Standard
b. Gasoline Aromatics Content Standard
c. Benzene Emission Standard
3. How Did We Select the Level of the Proposed Gasoline Benzene
Content Standard?
a. Current Gasoline Benzene Levels
b. The Need for an Average Benzene Standard
c. Potential Levels for the Average Benzene Standard
d. Comparison of Other Benzene Regulatory Programs
4. How Do We Address Variations in Refinery Benzene Levels?
a. Overall Reduction in Benzene Level and Variation
b. Consideration of an Upper Limit Standard
i. Per-Gallon Cap Standard
ii. Maximum Average Standard
5. How Would the Proposed Program Meet or Exceed Related
Statutory and Regulatory Requirements?
D. Description of the Proposed Averaging, Banking, and Trading
(ABT) Program
1. Overview
2. Standard Credit Generation (2011 and Beyond)
3. Credit Use
a. Credit Trading Area
b. Credit Life
4. Early Credit Generation (2007-2010)
a. Establishing Early Credit Baselines
b. Early Credit Reduction Criteria (Trigger Points)
c. Calculating Early Credits
5. Additional Credit Provisions
a. Credit Trading
b. Pre-Compliance Reporting Requirements
6. Special ABT Provisions for Small Refiners
E. Regulatory Flexibility Provisions for Qualifying Refiners
1. Hardship Provisions for Qualifying Small Refiners
a. Qualifying Small Refiners
i. Regulatory Flexibility for Small Refiners
ii. Rationale for Small Refiner Provisions
b. How Do We Propose to Define Small Refiners for the Purpose of
the Hardship Provisions?
c. What Options Would Be Available For Small Refiners?
i. Delay in Standards
ii. ABT Credit Generation Opportunities
iii. Extended Credit Life
iv. ABT Program Review
d. How Would Refiners Apply for Small Refiner Status?
[[Page 15807]]
e. The Effect of Financial and Other Transactions on Small
Refiner Status and Small Refiner Relief Provisions
2. General Hardship Provisions
a. Temporary Waivers Based on Unforeseen Circumstances
b. Temporary Waivers Based on Extreme Hardship Circumstances
c. Early Compliance with the Proposed Benzene Standard
F. Technological Feasibility of Gasoline Benzene Reduction
1. Benzene Levels in Gasoline
2. Technologies for Reducing Gasoline Benzene Levels
a. Why is Benzene Found in Gasoline?
b. Benzene Control Technologies Related to the Reformer
i. Routing Around the Reformer
ii. Routing to the Isomerization Unit
iii. Benzene Saturation
iv. Benzene Extraction
c. Other Benzene Reduction Technologies
d. Impacts on Octane and Strategies for Recovering Octane Loss
e. Experience Using Benzene Control Technologies
f. What Are the Potential Impacts of Benzene Control on Other
Fuel Properties?
3. Feasible Level of Benzene Control
4. Lead time
5. Issues
a. Small Refiners
b. Imported Gasoline
G. How Does the Proposed Fuel Control Program Satisfy the
Statutory Requirements?
H. Effect on Energy Supply, Distribution, or Use
I. How Would the Proposed Gasoline Benzene Standard Be
Implemented?
1. General provisions
a. What Are the Implementation Dates for the Proposed Program?
b. Which Regulated Parties Would Be Subject to the Proposed
Benzene Standards?
c. What Gasoline Would Be Subject to the Proposed Benzene
Standards?
d. How Would Compliance With the Benzene Standard Be Determined?
2. Averaging, Banking and Trading Program
a. Early Credit Generation
b. How Would Refinery Benzene Baselines Be Determined?
c. Credit Generation Beginning in 2011
d. How Would Credits Be Used?
3. Hardship and Small Refiner Provisions
a. Hardship
b. Small Refiners
4. Administrative and Enforcement Related Provisions
a. Sampling/Testing
b. Recordkeeping/Reporting
c. Attest Engagements, Violations, Penalties
5. How Would Compliance With the Provisions of the Proposed
Benzene Program Affect Compliance With Other Gasoline Toxics
Programs?
VIII. Gas Cans
A. Why Are We Proposing an Emissions Control Program for Gas
Cans?
1. VOC Emissions
2. Technological Opportunities to Reduce Emissions from Gas Cans
3. State Experiences Regulating Gas Cans
B. What Emissions Standard is EPA Proposing, and Why?
1. Description of Emissions Standard
2. Determination of Best Available Control
3. Emissions Performance vs. Design Standard
4. Automatic Shut-Off
5. Consideration of Retrofits of Existing Gas Cans
6. Consideration of Diesel, Kerosene and Utility Containers
C. Timing of Standard
D. What Test Procedures Would Be Used?
1. Diurnal Test
2. Preconditioning to Ensure Durable In-Use Control
a. Durability cycles
b. Preconditioning Fuel Soak
c. Spout Actuation
E. What Certification and In-Use Compliance Provisions Is EPA
Proposing?
1. Certification
2. Emissions Warranty and In-Use Compliance
3. Labeling
F. How Would State Programs Be Affected By EPA Standards?
G. Provisions for Small Gas Can Manufacturers
1. First Type of Hardship Provision
2. Second Type of Hardship Provision
IX. What are the Estimated Impacts of the Proposal?
A. Refinery Costs of Gasoline Benzene Reduction
1. Tools and Methodology
a. Linear Programming Cost Model
b. Refiner-by-Refinery Cost Model
c. Price of Chemical Grade Benzene
d. Applying the Cost Model to Special Cases
2. Summary of Costs
a. Nationwide Costs of the Proposed Program
b. Regional Distribution of Costs
c. Cost Effects of Different Standards
d. Effect on Cost Estimates of Higher Benzene Prices
3. Economic Impacts of MSAT Control Through Gasoline Sulfur and
RVP Control and a Total Toxics Standard
B. What Are the Vehicle Cost Impacts?
C. What Are The Gas Can Cost Impacts?
D. Cost Per Ton of Emissions Reduced
E. Benefits
1. Unquantified Health and Environmental Benefits
2. Quantified Human Health and Environmental Effects of the
Proposed Cold Temperature Vehicle Standard
3. Monetized Benefits
4. What Are the Significant Limitations of the Benefit Analysis?
5. How Do the Benefits Compare to the Costs of The Proposed
Standards?
F. Economic Impact Analysis
1. What Is an Economic Impact Analysis?
2. What Is the Economic Impact Model?
3. What Economic Sectors Are Included in this Economic Impact
Analysis?
4. What Are the Key Features of the Economic Impact Model?
5. What Are the Key Model Inputs?
6. What Are the Results of the Economic Impact Modeling?
X. Alternative Program Options
A. Fuels
B. Vehicles
C. Gas cans
XI. Public Participation
A. How Do I Submit Comments?
B. How Should I Submit CBI to the Agency?
C. Will There Be a Public Hearing?
D. Comment Period
E. What Should I Consider as I Prepare My Comments for EPA?
XII. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory Planning and Review
B. Paperwork Reduction Act
C. Regulatory Flexibility Act (RFA), as amended by the Small
Business Regulatory Enforcement Fairness Act of 1996 (SBREFA), 5
U.S.C. 601 et. seq
1. Overview
2. Background
3. Summary of Regulated Small Entities
a. Highway Light-Duty Vehicles
b. Gasoline Refiners
c. Portable Gasoline Container Manufacturers
4. Potential Reporting, Record Keeping, and Compliance
5. Relevant Federal Rules
6. Summary of SBREFA Panel Process and Panel Outreach
a. Significant Panel Findings
b. Panel Process
c. Small Business Flexibilities
i. Highway Light-Duty Vehicles
(a) Highway Light-Duty Vehicle Flexibilities
(b) Highway Light-Duty Vehicle Hardships
ii. Gasoline Refiners
(a) Gasoline Refiner Flexibilities
(b) Gasoline Refiner Hardships
iii. Portable Gasoline Containers
(a) Portable Gasoline Container Flexibilities
(b) Portable Gasoline Container Hardships
D. Unfunded Mandates Reform Act
E. Executive Order 13132: Federalism
F. Executive Order 13175: Consultation and Coordination With
Indian Tribal Governments
G. Executive Order 13045: Protection of Children from
Environmental Health and Safety Risks
H. Executive Order 13211: Actions that Significantly Affect
Energy Supply, Distribution, or Use
I. National Technology Transfer Advancement Act
J. Executive Order 12898: Federal Actions To Address
Environmental Justice in Minority Populations and Low-Income
Populations
XIII. Statutory Provisions and Legal Authority
I. Introduction
A. Summary
Mobile sources emit air toxics that can cause cancer and other
serious health effects. Section III of this preamble and Chapter 1 of
the
[[Page 15808]]
Regulatory Impact Analysis (RIA) for this rule describe these compounds
and their health effects. Mobile sources contribute significantly to
the nationwide risk from breathing outdoor sources of air toxics.
Mobile sources were responsible for about 44% of outdoor toxic
emissions, almost 50% of the cancer risk, and 74% of the noncancer risk
according to EPA's National-Scale Air Toxics Assessment (NATA) for
1999. In addition, people who live or work near major roads or live in
homes with attached garages are likely to have higher exposures and
risk, which are not reflected in NATA. Sections II.A and IV of this
preamble and Chapter 3 of the RIA provide more detail about NATA, as
well as our analysis of exposures near roadways.
According to NATA for 1999, there are a few mobile source air
toxics that pose the greatest risk based on current information about
ambient levels and exposure. These include benzene, 1,3-butadiene,
formaldehyde, acrolein, naphthalene, and polycyclic organic matter
(POM). All of these compounds are hydrocarbons except POM. Benzene is
the most significant contributor to cancer risk from all outdoor air
toxics, according to NATA for 1999. NATA does not include a
quantitative estimate of cancer risk for diesel exhaust, but it
concludes that diesel exhaust (specifically, diesel particulate matter
and diesel exhaust organic gases) is one of the pollutants that pose
the greatest relative cancer risk. Although we expect significant
reductions in mobile source air toxics in the future, cancer and
noncancer health risks will remain a public health concern, and
exposure to benzene will remain the largest contributor to this risk.
As discussed in detail in Section V of this preamble and Chapter 2
of the RIA, this proposal would significantly reduce emissions of the
many air toxics that are hydrocarbons, including benzene, 1,3-
butadiene, formaldehyde, acetaldehyde, acrolein, and naphthalene. The
proposed fuel benzene standard and hydrocarbon standards for vehicles
and gas cans would together reduce total emissions of mobile source air
toxics by 350,000 tons in 2030, including 65,000 tons of benzene.
Mobile sources were responsible for 68% of benzene emissions in 1999.
As a result of this proposal, in 2030 passenger vehicles would emit 45%
less benzene, gas cans would emit 78% less benzene, and the gasoline
would have 37% less benzene overall.
In addition, EPA has already taken significant steps to reduce
diesel emissions from mobile sources, which will result in a 70%
reduction between 1999 and 2020. We have adopted stringent standards
for diesel trucks and buses, and nonroad diesel engines (engines used,
for example, in construction, agricultural, and industrial
applications). We also have additional programs underway to reduce
diesel emissions, including voluntary programs and a proposal that is
being developed to reduce emissions from diesel locomotives and marine
engines.
The proposed reductions in mobile source air toxics emissions would
reduce exposure and predicted risk of cancer and noncancer health
effects, including in environments where exposure and risk may be
highest, such as near roads, in vehicles, and in homes with attached
garages. In addition, the hydrocarbon reductions from the vehicle and
gas can standards would reduce VOC emissions (which are a precursor to
ozone and PM2.5) by over 1 million tons in 2030. The
proposed vehicle standards would reduce direct PM2.5
emissions by 20,000 tons in 2030 and would also reduce secondary
formation of PM2.5. Although ozone and PM2.5 are
considered criteria pollutants rather than ``air toxics,'' reductions
in ozone and PM2.5 are important co-benefits of this
proposal. More details on emissions, cancer risks, and adverse health
and welfare effects associated with ozone and PM are found in sections
II.A, IV and V of this preamble and Chapters 2 and 3 of the RIA.
Section II.B of this preamble provides an overview of the
regulatory program that EPA is proposing for passenger vehicles,
gasoline, and gas cans. We are proposing standards to limit the exhaust
hydrocarbons from passenger vehicles during cold temperature operation.
We are also proposing evaporative hydrocarbon emissions standards for
passenger vehicles. We are proposing to limit the average annual
benzene content of gasoline. Finally, we are proposing hydrocarbon
emissions standards for gas cans that would reduce evaporation,
permeation, and spillage from these containers. Detailed discussion of
each of these programs is in sections VI, VII, and VIII of the preamble
and Chapters 5, 6, and 7 of the RIA.
We estimate that the benefits of this proposal would be about $6
billion in 2030, based on the direct PM2.5 reductions from
the vehicle standards, plus unquantified benefits from reductions in
mobile source air toxics and VOC. We estimate that the annual net
social costs of this proposal would be about $200 million in 2030
(expressed in 2003 dollars). These net social costs include the value
of fuel savings from the proposed gas can standards, which would be
worth $82 million in 2030.
The proposed reductions would have an average cost of 0.13 cents
per gallon of gasoline, less than $1 per vehicle, and less than $2 per
gas can. The reduced evaporation from gas cans would result in fuel
savings that would more than offset the increased cost for the gas can.
In 2030, the long-term cost per ton of the proposed standards (in
combination, and including fuel savings) would be $450 per ton of total
mobile source air toxics reduced; $2,400 per ton of benzene reduced;
and no cost for the hydrocarbon and PM reductions (because the vehicle
standards would have no cost in 2020 and beyond). Section IX of the
preamble and Chapters 8-13 of the RIA provide more details on the
costs, benefits, and economic impacts of the proposed standards. The
impacts on small entities and the flexibilities we are proposing are
discussed in section XII.C of this preamble and Chapter 14 of the RIA.
B. What Background Information is Helpful to Understand this Proposal?
1. What Are Air Toxics and Related Health Effects?
Air toxics, which are also known in the Clean Air Act as
``hazardous air pollutants,'' are those pollutants known or suspected
to cause cancer or other serious health or environmental effects. For
example, some of these pollutants are known to have negative effects on
people's respiratory, cardiovascular, neurological, immune,
reproductive, or other organ systems, and they may also have
developmental effects. They may pose particular hazards to more
susceptible and sensitive populations, such as children, the elderly,
or people with pre-existing illnesses.
Mobile source air toxics (MSATs) are those toxics emitted by motor
vehicles, nonroad engines (such as lawn and garden equipment, farming
and construction equipment, aircraft, locomotives, and ships), and
their fuels. Toxics are also emitted by stationary sources such as
power plants, factories, oil refineries, dry cleaners, gas stations,
and small manufacturers. They can also be produced by combustion of
wood and other organic materials. There are also indoor sources of air
toxics, such as solvent evaporation and outgassing from furniture and
building materials.
Some MSATs of particular concern include benzene, 1,3-butadiene,
formaldehyde, acrolein, naphthalene, and diesel particulate matter and
diesel exhaust organic gases. Benzene and 1,3-butadiene are both known
human
[[Page 15809]]
carcinogens. Section III of this preamble provides more detail on the
health effects of each of these pollutants.
MSATs are emitted as a result of various processes. Some MSATs are
present in fuel or fuel additives and are emitted to the air when the
fuel evaporates or passes through the engine. Some MSATs are formed
through engine combustion processes. Some compounds, like formaldehyde
and acetaldehyde, are also formed through a secondary process when
other mobile source pollutants undergo chemical reactions in the
atmosphere. Finally, some air toxics, such as metals, result from
engine wear or from impurities in oil or fuel.
2. What is the Statutory Authority for Today's Proposal?
a. Clean Air Act Section 202(l)
Section 202(l)(2) of the Clean Air Act requires EPA to set
standards to control hazardous air pollutants from motor vehicles,
motor vehicle fuels, or both. These standards must reflect the greatest
degree of emission reduction achievable through the application of
technology which will be available, taking into consideration the motor
vehicle standards established under section 202(a) of the Act, the
availability and cost of the technology, and noise, energy and safety
factors, and lead time. The standards are to be set under Clean Air Act
sections 202(a)(1) or 211(c)(1), and they are to apply, at a minimum,
to benzene and formaldehyde emissions.
Section 202(a)(1) of the Clean Air Act directs EPA to set standards
for new motor vehicles or new motor vehicle engines which EPA judges to
cause or contribute to air pollution which may reasonably be
anticipated to endanger public health or welfare. We are proposing a
cold-temperature hydrocarbon emission standard for passenger vehicles
under this authority.
Section 211(c)(1)(A) of the Clean Air Act authorizes EPA (among
other things) to control the manufacture of fuel if any emission
product of such fuel causes or contributes to air pollution which may
reasonably be anticipated to endanger public health or welfare. We are
proposing a benzene standard for gasoline under this authority.
Clean Air Act section 202(l)(2) requires EPA to ``from time to time
revise'' its regulations controlling hazardous air pollutants from
motor vehicles and fuels. As described in more detail in section I.F.
below, EPA has previously set standards under section 202(l), and we
committed in that rule to engage in further rulemaking to implement
section 202(l). This proposal fulfills that commitment.
b. Clean Air Act Section 183(e)
Clean Air Act section 183(e)(3) requires EPA to list categories of
consumer or commercial products that the Administrator determines,
based on an EPA study of VOC emissions from such products, contribute
at least 80 percent of the VOC emissions from such products in areas
violating the national ambient air quality standard for ozone. EPA
promulgated this list at 60 FR 15264 (March 23, 1995). EPA plans to
publish a Federal Register notice announcing that EPA has added
portable gasoline containers to the list of consumer products to be
regulated. This action must be taken by EPA prior to issuing a final
rule for gas cans. EPA is required to develop rules reflecting ``best
available controls'' to reduce VOC emissions from the listed products.
``Best available controls'' are defined in section 183(e)(1)(A) as
follows:
The term ``best available controls'' means the degree of
emissions reduction that the Administrator determines, on the basis
of technological and economic feasibility, health, environmental,
and energy impacts, is achievable through the application of the
most effective equipment, measures, processes, methods, systems, or
techniques, including chemical reformulation, product or feedstock
substitution, repackaging, and directions for use, consumption,
storage, or disposal.''
Section 183(e)(4) also allows these standards to be implemented by
means of ``any system or systems of regulation as the Administrator may
deem appropriate, including requirements for registration and labeling,
self-monitoring and reporting * * * concerning the manufacture,
processing, distribution, use, consumption, or disposal of the
product.'' We are proposing a hydrocarbon standard for gas cans under
the authority of section 183(e).
c. Energy Policy Act
Section 1504(b) of the Energy Policy Act of 2005 requires EPA to
adjust the toxics emissions baselines for reformulated gasoline to
reflect 2001-2002 fuel qualities. However, the Act provides that this
action becomes unnecessary if EPA takes action which results in greater
overall reductions of toxics emissions from vehicles in areas with
reformulated gasoline. As described in section VII of this preamble, we
believe today's proposed action would in fact result in greater
reductions than would be achieved by adjusting the baselines under the
Energy Policy Act. Accordingly, under the provisions of the Energy
Policy Act, this proposed action would obviate the need for readjusting
emissions baselines for reformulated gasoline.
3. What Other Actions Has EPA Taken Under Clean Air Act Section 202(l)?
a. 2001 Mobile Source Air Toxics Rule
EPA published a final rule under Clean Air Act section 202(l) on
March 29, 2001, entitled, ``Control of Emissions of Hazardous Air
Pollutants from Mobile Sources'' (66 FR 17230). This rule established
toxics emissions performance standards for gasoline refiners. These
standards were designed to ensure that the over compliance to the
standard seen in the in-use fuels produced in the years of 1998-2000
would continue in the future.
EPA adopted this anti-backsliding requirement as a near-term
control that could be implemented and take effect within a year or two.
We did not adopt long-term controls, those controls that require a
longer lead time to implement, because we lacked information to address
the costs and benefits of potential fuel controls in the context of the
fuel sulfur controls that we had finalized in February 2000. However,
the March 2001 rule did commit to additional rulemaking that would
evaluate the need for and feasibility of additional controls.\1\
Today's proposal fulfills that commitment, and represents the second
step of the two-step approach originally envisioned in the 2001 rule.
---------------------------------------------------------------------------
\1\ See Sierra Club v. EPA, 325 F. 3d 374, 380 (D.C. Cir. 2003),
which upholds this approach.
---------------------------------------------------------------------------
The 2001 rule did not set additional air toxics controls for motor
vehicles, because the technology-forcing Tier 2 light-duty vehicle
standards and 2007 heavy-duty engine and vehicle standards had just
been promulgated. We found that those standards represented the
greatest degree of toxics control achievable at that time under section
202(l).\2\
---------------------------------------------------------------------------
\2\ 66 FR 17241-17245 (March 29, 2001).
---------------------------------------------------------------------------
b. Technical Analysis Plan
The 2001 rulemaking also included a Technical Analysis Plan that
described toxics-related research and activities that would inform our
future rulemaking to evaluate the need for and appropriateness of
additional mobile source air toxic controls. Specifically, we
identified four critical areas where there were data gaps requiring
long-term efforts:
Developing better air toxics emission factors for nonroad
sources;
Improving estimation of air toxics exposures in
microenvironments;
[[Page 15810]]
Improving consideration of the range of total public
exposures to air toxics; and
Increasing our understanding of the effectiveness and
costs of vehicle, fuel and nonroad controls for air toxics.
EPA and other outside researchers have conducted significant
research in these areas since 2001. The findings of this research are
described in more detail in other sections of this preamble and in the
regulatory impact analysis for this proposal. Following are some
highlights of our activities.
Nonroad emissions testing. EPA has tested emissions of nonroad
diesel engines for a comprehensive suite of hydrocarbons and inorganic
compounds. These emissions tests employed steady-state as well as
transient test cycles, using typical nonroad diesel fuel and low-sulfur
nonroad diesel fuel. In addition, EPA tested small gasoline-powered
engines such as lawnmowers, leaf blowers, chainsaws and string
trimmers.
Improved estimation of exposures in microenvironments and
consideration of the range of public exposures. EPA and other
researchers have conducted a substantial amount of research and
analysis in these areas, which is discussed in section IV of this
preamble and in the regulatory impact analysis. This research has
involved monitoring as well as the development and application of
enhanced modeling tools. For example, personal exposure monitoring and
ambient monitoring has been conducted at homes and schools near
roadways; in vehicles; in homes with attached garages; and in
occupational settings involving both diesel and gasoline nonroad
equipment. We have also applied dispersion modeling techniques with
greater spatial refinement to estimate gradients of toxic pollutants
near roadways. A variety of improvements to our emissions, dispersion,
and exposure modeling tools are improving our ability to consider the
range of exposure people experience. These include the MOBILE6
emissions model, improved spatial and temporal allocation of emissions,
development of the Community Multiscale Air Quality (CMAQ) model, and
updates to the HAPEM exposure model. Many of these improvements were
applied in EPA's National-Scale Air Toxics Assessment for 1999 and
other analyses EPA performed to support this proposal. In fact, EPA
developed a modification of the HAPEM exposure model to account for
higher pollutant concentrations near major roads.
Research in these areas is continuing both inside and outside EPA,
including work under the auspices of the Health Effects Institute and
the Mickey Leland National Urban Air Toxics Research Center.
Costs and effectiveness of vehicle, fuel, and nonroad controls for
air toxics. EPA's analysis of the costs and effectiveness of vehicle
and fuel controls is described in section IX of this preamble and in
the regulatory impact analysis. In addition, as described in section V,
EPA is currently developing rules that will examine controls of small
gasoline engines and diesel locomotive and marine engines.
II. Overview of Proposal
A. Why Is EPA Making This Proposal?
People experience elevated risk of cancer and other noncancer
health effects from exposure to air toxics. Mobile sources are
responsible for a significant portion of this risk. For example,
benzene is the most significant contributor to cancer risk from all
outdoor air toxics,\3\ and most of the nation's benzene emissions come
from mobile sources. These risks vary depending on where people live
and work and the kinds of activities in which they engage. People who
live or work near major roads, or people that spend a large amount of
time in vehicles, are likely to have higher exposures and higher risks.
Although we expect significant reductions in mobile source air toxics
in the future, predicted cancer and noncancer health risks will remain
a public health concern. Benzene will remain the largest contributor to
this risk. In addition, some mobile source air toxics contribute to the
formation of ozone and PM2.5, which contribute to serious
public health problems, which are discussed further in section II.A.4.
---------------------------------------------------------------------------
\3\ Based on quantitative estimates of risk, which do not
include diesel particular matter and diesel exhaust organic gases.
---------------------------------------------------------------------------
Sections II.A.1-3 discuss the risks posed by outdoor toxics now and
in the future, based on national-scale estimates such as EPA's
National-Scale Air Toxics Assessment (NATA). EPA's NATA for 1999
provides some perspective on the average risk of cancer and noncancer
health effects resulting from breathing air toxics from outdoor
sources, and the contribution of mobile sources to these
risks.4 5 This assessment did not include indoor sources of
air toxics. Also, it estimates average concentrations within a census
tract, and therefore does not reflect elevated concentrations and
exposures near roadways within a census tract. Nevertheless, its
findings are useful in providing a perspective on the magnitude of
risks posed by outdoor sources of air toxics generally, and in
identifying what pollutants and sources are important contributors to
these health risks.
---------------------------------------------------------------------------
\4\ https://www.epa.gov/ttn/atw/nata 1999.
\5\ NATA does not include a quantitative estimate of cancer risk
for diesel particulate matter and diesel exhaust organic gases. EPA
has concluded that while diesel exhaust is likely to be a human
carcinogen, available data are not sufficient to develop a
confidential estimate of cancer unit risk.
---------------------------------------------------------------------------
EPA also performed a national-scale assessment for future years,
using the same modeling tools and approach as the 1999 NATA. Finally,
we also performed national-scale exposure modeling that accounts for
the higher toxics concentrations near roads. This latter modeling
provides a perspective on the mobile source contribution to risk from
air toxics that is not reflected in our other national-scale
assessments.
1. National Cancer Risk from Air Toxics
According to NATA, the average national cancer risk in 1999 from
all outdoor sources of air toxics was 42 in a million. That is, 42 out
of one million people would be expected to contract cancer from a
lifetime of breathing air toxics at 1999 levels. Mobile sources were
responsible for 44% of outdoor toxic emissions and almost 50% of the
cancer risk. Considering only the subset of compounds emitted by mobile
sources (see Table IV.C-2), the national average cancer risk in 1999,
including the stationary source contribution to these pollutants, was
23 in a million.
Benzene is the largest contributor to cancer risk of all 133
pollutants quantitatively assessed in the 1999 NATA. The national
average cancer risk from benzene alone was 11 in a million. Over 120
million people in 1999 were exposed to a risk level above 10 in a
million due to chronic inhalation exposure to benzene. Mobile sources
were responsible for 68% of benzene emissions in 1999.
Although air toxics emissions are projected to decline in the
future as a result of standards EPA has previously adopted, cancer risk
will continue to be a public health concern. The predicted national
average cancer risk from MSATs in 2030 will be 18 in a million,
according to EPA analysis (described in more detail in section IV of
this preamble and Chapter 3 of the Regulatory Impact Analysis). In
fact, in 2030 there will be more people exposed to the highest levels
of risk. The number of Americans above the 10 in a million cancer risk
level from exposure to MSATs is projected to increase from 214 million
in 1999 to 240 million in 2030. Mobile sources will continue to be a
significant contributor to risk in the future, accounting for 22% of
total air
[[Page 15811]]
toxic emissions in 2020, and 44% of benzene emissions.
2. Noncancer Health Effects
According to the NATA for 1999, nearly the entire U.S. population
was exposed to an average level of air toxics that has the potential
for adverse respiratory health effects (noncancer).\6\ This will
continue to be the case in 2030, even though toxics levels will be
lower.
---------------------------------------------------------------------------
\6\ That is, the respiratory hazard index exceeded 1. See
section III.D of this preamble for more information.
---------------------------------------------------------------------------
Mobile sources were responsible for 74% of the noncancer
(respiratory) risk from outdoor air toxics in 1999. The majority of
this risk was from acrolein, and formaldehyde also contributed to the
risk of respiratory health effects. Mobile sources will continue to be
responsible for the majority of noncancer risk from outdoor air toxics
in 2030.
Although not included in NATA's estimates of noncancer risk, PM
from gasoline and diesel mobile sources contribute significantly to the
health effects associated with ambient PM, for which EPA has
established a National Ambient Air Quality Standard. There is extensive
human data showing a wide spectrum of adverse health effects associated
with exposure to ambient PM.
3. Exposure Near Roads and From Attached Garages
The national-scale risks described above do not account for higher
exposures experienced by people who live near major roadways, or people
who live in homes with attached garages. A substantial number of
studies show elevated concentrations of multiple MSATs in close
proximity to major roads. We also conducted an exposure modeling study
for three geographically distinct states (Colorado, New York, and
Georgia) and found that when the elevated concentrations near roadways
are accounted for, the distribution of benzene exposure is broader,
with a larger fraction of the population exposed to higher
concentrations. The largest effect on personal exposure occurs for the
population living near major roads. A U.S. Census survey of housing
found that in 2003 12.6% of U.S. housing units were within 300 feet of
a major transportation source.\7\ The potential population exposed to
elevated concentrations near major roadways is therefore large. In
addition, our analysis indicates that benzene exposure experienced by
people living in homes with attached garages may be twice the national
average benzene exposure estimated by NATA for 1999. More details on
exposure near roads and from attached garages can be found in section
IV of this preamble.
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\7\ United States Census Bureau. (2004) American Housing Survey
web page. [Online at https://www.cenus.gov/hhes/www/housing/ahs/
ahs03/ahs03.html] Table IA-6.
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4. Ozone and Particulate Matter
Many MSATs are part of a larger category of mobile source emissions
known as volatile organic compounds (VOC), which contribute to the
formation of ozone and particulate matter (PM). In addition, some MSATs
are emitted directly as PM rather than being formed through secondary
processes. Thus, MSATs contribute to adverse health effects both as
individual pollutants, and as precursors to ozone and PM. Mobile
sources contribute significantly to national emissions of VOC and PM.
In addition, gas cans are a source of both VOC and benzene emissions.
Both ozone and PM contribute to serious public health problems,
including premature mortality, aggravation of respiratory and
cardiovascular disease (as indicated by increased hospital admissions
and emergency room visits, school absences, work loss days, and
restricted activity days), changes in lung function and increased
respiratory symptoms, changes to lung tissues and structures, altered
respiratory defense mechanisms, chronic bronchitis, and decreased lung
function.
In addition, ozone and PM cause significant harm to public welfare.
Specifically, ozone causes damage to vegetation, which leads to crop
and forestry economic losses, as well as harm to national parks,
wilderness areas, and other natural systems. PM contributes to the
substantial impairment of visibility in many parts of the U.S.,
including national parks and wilderness areas. The deposition of
airborne particles can also reduce the aesthetic appeal of buildings
and culturally important articles through soiling, and can contribute
directly (or in conjunction with other pollutants) to structural damage
by means of corrosion or erosion.
Finally, atmospheric deposition and runoff of polycyclic organic
matter (POM), metals, and other mobile-source-related compounds
contribute to the contamination of water bodies such as the Great Lakes
and coastal waters (e.g., the Chesapeake Bay).
B. What Is EPA Proposing?
1. Light-Duty Vehicle Emission Standards
As described in more detail in section VI, we are proposing new
standards for both exhaust and evaporative emissions from passenger
vehicles. The new exhaust emissions standards would significantly
reduce non-methane hydrocarbon (NMHC) emissions from passenger vehicles
at cold temperatures. These hydrocarbons include many mobile source air
toxics (including benzene), as well as VOC.
Current vehicle emission standards require that the certification
testing of NMHC is performed at 75 [deg]F. Recent research and analysis
indicates that these standards are not resulting in robust control of
NMHC at lower temperatures. We believe that cold temperature NMHC
control can be substantially improved using the same technological
approaches that are generally already being used in the Tier 2 vehicle
fleet to meet the stringent standards at 75 [deg]F. These cold-
temperature NMHC controls would also result in lower direct PM
emissions at cold temperatures.
Accordingly, we are proposing that light-duty vehicles, light-duty
trucks, and medium-duty passenger vehicles would be subject to a new
non-methane hydrocarbon (NMHC) exhaust emissions standard at 20 [deg]F.
Vehicles at or below 6,000 pounds gross vehicle weight rating (GVWR)
would be subject to a sales-weighted fleet average NMHC level of 0.3
grams/mile. Vehicles between 6,000 and 8,500 pounds GVWR and medium-
duty passenger vehicles would be subject to a sales-weighted fleet
average NMHC level of 0.5 grams/mile. For lighter vehicles, the
standard would phase in between 2010 and 2013. For heavier vehicles,
the new standards would phase in between 2012 and 2015. We are also
proposing a credit program and other provisions designed to provide
flexibility to manufacturers, especially during the phase-in periods.
These provisions are designed to allow the earliest possible phase-in
of standards and help minimize costs and ease the transition to new
standards.
We are also proposing a set of nominally more stringent evaporative
emission standards for all light-duty vehicles, light-duty trucks, and
medium-duty passenger vehicles. The proposed standards are equivalent
to California's Low Emission Vehicle II (LEV II) standards, and they
reflect the evaporative emissions levels that are already being
achieved nationwide. The standards we are proposing today would codify
the approach that most
[[Page 15812]]
manufacturers are already taking for 50-state evaporative systems, and
the standards would thus prevent backsliding in the future. We are
proposing to implement the evaporative emission standards in 2009 for
lighter vehicles and in 2010 for the heavier vehicles.
Section VI provides details on the proposed exhaust and evaporative
standards and their implementation, and our rationale for proposing
them.
2. Gasoline Fuel Standards
As described in more detail in section VII, we are proposing to
limit the benzene content of all gasoline, both reformulated and
conventional. We propose that beginning January 1, 2011, refiners would
meet an average gasoline benzene content standard of 0.62% by volume on
all their gasoline. We are not proposing a standard for California,
however, because it is already covered by a similar state program.
This proposed fuel standard would result in air toxics emissions
reductions that are greater than required under all existing gasoline
toxics programs. As a result, EPA is proposing that upon full
implementation in 2011, the regulatory provisions for the benzene
control program would become the single regulatory mechanism used to
implement the RFG and Anti-dumping annual average toxics requirements.
The current RFG and Anti-dumping annual average provisions thus would
be replaced by the proposed benzene control program. The MSAT2 benzene
control program would also replace the MSAT1 requirements. In addition,
the program would satisfy certain fuel MSAT conditions of the Energy
Policy Act of 2005 and obviate the need to revise toxics baselines for
reformulated gasoline otherwise required by the Energy Policy Act. In
all of these ways, we would significantly consolidate and simplify the
existing national fuel-related MSAT regulatory program.
We also propose that refiners could generate benzene credits and
use or transfer them as a part of a nationwide averaging, banking, and
trading (ABT) program. From 2007-2010 refiners could generate benzene
credits by taking early steps to reduce gasoline benzene levels.
Beginning in 2011 and continuing indefinitely, refiners could generate
credits by producing gasoline with benzene levels below the 0.62%
average standard. Refiners could apply the credits towards company
compliance, ``bank'' the credits for later use, or transfer (``trade'')
them to other refiners nationwide (outside of California) under the
proposed program. Under this program, refiners could use credits to
achieve compliance with the benzene content standard.
This proposed ABT program would allow us to set a more stringent
benzene standard than would otherwise be possible, and it would allow
implementation to occur earlier. Under this proposed benzene content
standard and ABT program, gasoline in all areas of the country would
have lower benzene levels than they have today. Overall benzene levels
would be 37% lower. This would reduce benzene emissions and exposure
nationwide.
Finally, we propose hardship provisions. Refiners approved as
``small refiners'' would be eligible for certain temporary relief
provisions. In addition, any refiner facing extreme unforeseen
circumstances or extreme hardship circumstances could apply for similar
temporary relief.
Section VII of this preamble provides a detailed explanation and
rationale for the proposed fuel program and its implementation. It also
discusses and seeks comment on a variety of alternatives that we
considered.
3. Portable Gasoline Container (Gas Can) Controls
Portable gasoline containers, or gas cans, are consumer products
used to refuel a wide variety of gasoline-powered equipment, including
lawn and garden equipment, recreational equipment, and passenger
vehicles that have run out of gas. As described in section VIII, we are
proposing standards that would reduce hydrocarbon emissions from
evaporation, permeation, and spillage. These standards would
significantly reduce benzene and other toxics, as well as VOC more
generally. VOC is an ozone precursor.
We propose a performance-based standard of 0.3 grams per gallon per
day of hydrocarbons, based on the emissions from the can over a diurnal
test cycle. The standard would apply to gas cans manufactured on or
after January 1, 2009. We also propose test procedures and a
certification and compliance program, in order to ensure that gas cans
would meet the emission standard over a range of in-use conditions. The
proposed standards would result in the use of best available control
technologies, such as durable permeation barriers, automatically
closing spouts, and cans that are well-sealed.
California implemented an emissions control program for gas cans in
2001, and since then, several other states have adopted the program.
Last year, California adopted a revised program, which will take effect
July 1, 2007. The revised California program is very similar to the
program we are proposing. Although a few aspects of the program we are
proposing are different, we believe manufacturers would be able to meet
both EPA and California requirements with the same gas can designs.
III. What Are Mobile Source Air Toxics (MSATs) and Their Health
Effects?
A. What Are MSATs?
Section 202(l) refers to ``hazardous air pollutants from motor
vehicles and motor vehicle fuels.'' We use the term ``mobile source air
toxics (MSATs)'' to refer to compounds that are emitted by mobil