National Emission Standards for Aerospace Manufacturing and Rework Facilities Risk and Technology Review, 8391-8439 [2015-02055]
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Vol. 80
Tuesday,
No. 31
February 17, 2015
Part II
Environmental Protection Agency
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40 CFR Part 63
National Emission Standards for Aerospace Manufacturing and Rework
Facilities Risk and Technology Review; Proposed Rule
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Federal Register / Vol. 80, No. 31 / Tuesday, February 17, 2015 / Proposed Rules
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 63
[EPA–HQ–OAR–2014–0830; FRL–9922–10–
OAR]
RIN 2060–AQ99
National Emission Standards for
Aerospace Manufacturing and Rework
Facilities Risk and Technology Review
Environmental Protection
Agency.
ACTION: Proposed rule.
AGENCY:
The Environmental Protection
Agency (EPA) is proposing amendments
to the national emissions standards for
hazardous air pollutants (NESHAP) for
Aerospace Manufacturing and Rework
Facilities to address the results of the
residual risk and technology review
(RTR) conducted as required under the
Clean Air Act (CAA), and to correct
errors and deficiencies identified during
the review of these standards. The
proposed amendments would add
limitations to reduce organic and
inorganic emissions of hazardous air
pollutants (HAP) from specialty coating
application operations; would remove
the exemptions from the emission
limitations for periods of startup,
shutdown and malfunction (SSM) so
that affected units would be subject to
the emission standards at all times; and
would revise provisions to address
recordkeeping and reporting
requirements applicable to periods of
SSM. This action also proposes other
technical corrections. The EPA
estimates that implementation of this
proposed rule will result in reductions
of 58 tons of HAP.
DATES: Comments. Comments must be
received on or before April 3, 2015. A
copy of comments on the information
collection provisions should be
submitted to the Office of Management
and Budget (OMB) on or before March
19, 2015.
Public Hearing. If anyone contacts the
EPA requesting a public hearing by
February 23, 2015, we will hold a public
hearing on March 4, 2015. If you are
interested in requesting a public hearing
or attending the public hearing, contact
Ms. Pamela Garrett at (919) 541–7966 or
at garrett.pamela@epa.gov. If the EPA
holds a public hearing, the EPA will
keep the record of the hearing open for
30 days after completion of the hearing
to provide an opportunity for
submission of rebuttal and
supplementary information.
ADDRESSES: Comments. Submit your
comments, identified by Docket ID No.
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SUMMARY:
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EPA–HQ–OAR–2014–0830, by one of
the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
• Email: A-and-R-Docket@epa.gov.
Include Attention Docket ID No. EPA–
HQ–OAR–2014–0830 in the subject line
of the message.
• Fax: (202) 566–9744, Attention
Docket ID No. EPA–HQ–OAR–2014–
0830.
• Mail: Environmental Protection
Agency, EPA Docket Center (EPA/DC),
Mail Code 28221T, Attention Docket ID
No. EPA–HQ–OAR–2014–0830, 1200
Pennsylvania Avenue 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 Street NW., Washington,
DC 20503.
• Hand/Courier Delivery: EPA Docket
Center, Room 3334, EPA WJC West
Building, 1301 Constitution Avenue
NW., Washington, DC 20004, Attention
Docket ID No. EPA–HQ–OAR–2014–
0830. 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–2014–
0830. The EPA’s policy is that all
comments received will be included in
the public docket without change and
may be made available online at
https://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 https://
www.regulations.gov or email. The
https://www.regulations.gov Web site is
an ‘‘anonymous access’’ system, which
means the EPA will not know your
identity or contact information unless
you provide it in the body of your
comment. If you send an email
comment directly to the EPA without
going through https://
www.regulations.gov, your email
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, the 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 the EPA
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cannot read your comment due to
technical difficulties and cannot contact
you for clarification, the EPA may not
be able to consider your comment.
Electronic files should not include
special characters or any form of
encryption and be free of any defects or
viruses. For additional information
about the EPA’s public docket, visit the
EPA Docket Center homepage at:
https://www.epa.gov/dockets.
Docket. The EPA has established a
docket for this rulemaking under Docket
ID No. EPA–HQ–OAR–2014–0830. All
documents in the docket are listed in
the https://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, is not placed on
the Internet and will be publicly
available only in hard copy. Publicly
available docket materials are available
either electronically in regulations.gov
or in hard copy at the EPA Docket
Center, Room 3334, EPA WJC West
Building, 1301 Constitution Avenue
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 EPA Docket Center is
(202) 566–1742.
Public Hearing. If a public hearing is
requested by February 23, 2015, it will
be held on March 4, 2015 at the EPA’s
Research Triangle Park Campus, 109
T.W. Alexander Drive, Research
Triangle Park, NC 27711. The hearing
will convene at 10:00 a.m. (Eastern
Standard Time) and end at 5:00 p.m.
(Eastern Standard Time). A lunch break
will be held from 12:00 p.m. (Eastern
Standard Time) until 1:00 p.m. (Eastern
Standard Time). Please contact Ms.
Pamela Garrett at (919) 541–7966 or at
garrett.pamela@epa.gov to request a
hearing, to determine if a hearing will
be held and to register to speak at the
hearing, if one is held. If a hearing is
requested, the last day to pre-register in
advance to speak at the hearing will be
March 2, 2015.
Additionally, requests to speak will
be taken the day of the hearing at the
hearing registration desk, although
preferences on speaking times may not
be able to be fulfilled. If you require the
service of a translator or special
accommodations such as audio
description, please let us know at the
time of registration. If you require an
accommodation, we ask that you
preregister for the hearing, as we may
not be able to arrange such
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accommodations without advance
notice.
If no one contacts the EPA requesting
a public hearing to be held concerning
this proposed rule by February 23, 2015,
a public hearing will not take place. If
a hearing is held, it will provide
interested parties the opportunity to
present data, views or arguments
concerning the proposed action. The
EPA will make every effort to
accommodate all speakers who arrive
and register. Because the hearing will be
held at a U.S. governmental facility,
individuals planning to attend the
hearing should be prepared to show
valid picture identification to the
security staff in order to gain access to
the meeting room. Please note that the
REAL ID Act, passed by Congress in
2005, established new requirements for
entering federal facilities. If your
driver’s license is issued by Alaska,
American Samoa, Arizona, Kentucky,
Louisiana, Maine, Massachusetts,
Minnesota, Montana, New York,
Oklahoma or the state of Washington,
you must present an additional form of
identification to enter the federal
building. Acceptable alternative forms
of identification include: federal
employee badges, passports, enhanced
driver’s licenses and military
identification cards. In addition, you
will need to obtain a property pass for
any personal belongings you bring with
you. Upon leaving the building, you
will be required to return this property
pass to the security desk. No large signs
will be allowed in the building, cameras
may only be used outside of the
building and demonstrations will not be
allowed on federal property for security
reasons.
The EPA may ask clarifying questions
during the oral presentations, but will
not respond to the presentations at that
time. Written statements and supporting
information submitted during the
comment period will be considered
with the same weight as oral comments
and supporting information presented at
the public hearing. Commenters should
notify Ms. Garrett if they will need
specific equipment, or if there are other
special needs related to providing
comments at the hearing. Verbatim
transcripts of the hearings and written
statements will be included in the
docket for the rulemaking. The EPA will
make every effort to follow the schedule
as closely as possible on the day of the
hearing; however, please plan for the
hearing to run either ahead of schedule
or behind schedule. Again, a hearing
will not be held unless requested.
FOR FURTHER INFORMATION CONTACT: For
questions about this proposed action,
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contact Kim Teal, Sector Policies and
Programs Division (D243–02), Office of
Air Quality Planning and Standards,
U.S. Environmental Protection Agency,
Research Triangle Park, North Carolina
27711; telephone number: (919) 541–
5580; fax number: (919) 541–5450; and
email address: teal.kim@epa.gov. For
specific information regarding the risk
modeling methodology, contact Ted
Palma, Health and Environmental
Impacts Division (C539–02), Office of
Air Quality Planning and Standards,
U.S. Environmental Protection Agency,
Research Triangle Park, North Carolina
27711; telephone number: (919) 541–
5470; fax number: (919) 541–0840; and
email address: palma.ted@epa.gov. For
information about the applicability of
the NESHAP to a particular entity,
contact Rafael Sanchez, Office of
Enforcement and Compliance Assurance
(OECA), (202) 564–7028,
sanchez.rafael@epa.gov.
SUPPLEMENTARY INFORMATION:
Preamble Acronyms and
Abbreviations. We use multiple
acronyms and terms in this preamble.
While this list may not be exhaustive, to
ease the reading of this preamble and for
reference purposes, the EPA defines the
following terms and acronyms here:
AD Airworthiness Directive
AEGL acute exposure guideline level
AERMOD air dispersion model used by the
HEM–3 model
ATSDR Agency for Toxic Substances and
Disease Registry
BACT Best Achievable Control Technology
CAA Clean Air Act
CalEPA California EPA
CBI Confidential Business Information
CDX EPA’s Central Data Exchange
CEDRI EPA’s Compliance and Emissions
Data Reporting Interface
CFR Code of Federal Regulations
CTG Control Technique Guideline
document
EJ environmental justice
EPA Environmental Protection Agency
ERPG Emergency Response Planning
Guidelines
ERT EPA’s Electronic Reporting Tool
FAA Federal Aviation Administration
FR Federal Register
g/L grams/liter
HAP hazardous air pollutants
HCl hydrochloric acid
HEM–3 Human Exposure Model, Version
1.1.0
HF hydrogen fluoride
HI hazard index
HQ hazard quotient
HVLP high volume low pressure
IARC International Agency for Research on
Cancer
ICR information collection request
IRIS Integrated Risk Information System
km kilometer
lb/gal pounds/gallon
LOAEL Lowest-observed-adverse-effect
level
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MACT maximum achievable control
technology
mg/m3 milligrams per cubic meter
MIR maximum individual risk
mm Hg millimeters mercury
NAAQS National Ambient Air Quality
Standards
NAICS North American Industry
Classification System
NAS National Academy of Sciences
NATA National Air Toxics Assessment
NEI National Emission Inventory
NESHAP National Emissions Standards for
Hazardous Air Pollutants
NOAA National Oceanic and Atmospheric
Administration
NOAEL No-observed-adverse-effect levels
NRC National Research Council
NRDC Natural Resources Defense Council
NTP National Toxicology Program
NTTAA National Technology Transfer and
Advancement Act
OAQPS Office of Air Quality Planning and
Standards
OECA Office of Enforcement and
Compliance Assurance
OEM original equipment manufacturer
OMB Office of Management and Budget
PAH polycyclic aromatic hydrocarbons
PB–HAP hazardous air pollutants known to
be persistent and bio-accumulative in the
environment
PEL Probable effect level
POM polycyclic organic matter
ppm parts per million
PSD Prevention of Significant Deterioration
RACT Reasonably Available Control
Technology
RBLC EPA’s RACT/BACT/LAER
Clearinghouse
RCRA Resource Conservation and Recovery
Act of 1976
REL reference exposure level
RFA Regulatory Flexibility Act
RfC reference concentration
RfD reference dose
RoC Report of the Carcinogens
RTR residual risk and technology review
SAB Science Advisory Board
SCAQMD South Coast Air Quality
Management District
SSM startup, shutdown and malfunction
TOSHI target organ-specific hazard index
tpy tons per year
TRIM.FaTE Total Risk Integrated
Methodology.Fate, Transport, and
Ecological Exposure model
TTN Technology Transfer Network
UF uncertainty factor
mg/m3 microgram per cubic meter
UMRA Unfunded Mandates Reform Act
URE unit risk estimate
VOC volatile organic compounds
Organization of this Document. The
information in this preamble is
organized as follows:
I. General Information
A. Does this action apply to me?
B. Where can I get a copy of this document
and other related information?
C. What should I consider as I prepare my
comments for the EPA?
II. Background
A. What is the statutory authority for this
action?
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B. What is this source category and how
does the current NESHAP regulate its
HAP emissions?
C. What data collection activities were
conducted to support this action?
D. What other relevant background
information and data are available?
E. What litigation is related to this
proposed action?
III. Analytical Procedures
A. How did we estimate post-MACT risks
posed by the source category?
B. How did we consider the risk results in
making decisions for this proposal?
C. How did we perform the technology
review?
IV. Analytical Results and Proposed
Decisions
A. What actions are we taking pursuant to
CAA sections 112(d)(2) and 112(d)(3)?
B. What are the results of the risk
assessment and analyses?
C. What are our proposed decisions
regarding risk acceptability, ample
margin of safety and adverse
environmental effects?
D. What are the results and proposed
decisions based on our technology
review?
E. What other actions are we proposing?
F. What compliance dates are we
proposing?
V. Summary of Cost, Environmental and
Economic Impacts
A. What are the affected sources?
B. What are the air quality impacts?
C. What are the cost impacts?
D. What are the economic impacts?
E. What are the benefits?
VI. Request for Comments
VII. Submitting Data Corrections
VIII. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory
Planning and Review and Executive
Order 13563: Improving Regulation and
Regulatory Review
B. Paperwork Reduction Act
C. Regulatory Flexibility Act (RFA)
D. Unfunded Mandates Reform Act
(UMRA)
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
Risks and Safety Risks
H. Executive Order 13211: Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution or Use
I. National Technology Transfer and
Advancement Act (NTTAA)
J. Executive Order 12898: Federal Actions
to Address Environmental Justice in
Minority Populations and Low-Income
Populations
I. General Information
A. Does this action apply to me?
is the subject of this proposal. Table 1
is not intended to be exhaustive, but
rather to provide a guide for readers
regarding the entities that this proposed
action is likely to affect. The proposed
standards, once promulgated, will be
directly applicable to the affected
sources. Federal government entities
may be affected by this proposed action.
Parties potentially affected by this
action include major and synthetic
minor source installations that are
owned or operated by the Armed Forces
of the United States (including the
Department of Defense and the Coast
Guard) and the National Aeronautics
and Space Administration. As defined
under the ‘‘Surface Coating’’ industry
sector in the ‘‘Initial List of Categories
of Sources Under Section 112(c)(1) of
the Clean Air Act Amendments of 1990’’
(see 57 FR 31576, July 16, 1992), the
Aerospace Manufacturing and Rework
Facilities source category is any facility
engaged, either in part or in whole, in
the manufacture or rework of
commercial, civil or military aerospace
vehicles or components and that are
major sources as defined in 40 CFR 63.2.
Table 1 of this preamble lists the
regulated industrial source category that
TABLE 1—INDUSTRIAL SOURCE CATEGORY AFFECTED BY THIS PROPOSED ACTION
Source Category
NESHAP
NAICS code a
Aerospace Manufacturing and Rework Facilities
Aerospace Manufacturing and Rework Facilities.
336411, 336412, 336413, 336414, 336415,
336419, 481111, 481112, 481211, 481212,
481219.
a North
American Industry Classification System.
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B. Where can I get a copy of this
document and other related
information?
In addition to being available in the
docket, an electronic copy of this action
is available on the Internet through the
EPA’s Technology Transfer Network
(TTN) Web site, a forum for information
and technology exchange in various
areas of air pollution control. Following
signature by the EPA Administrator, the
EPA will post a copy of this proposed
action at: https://www.epa.gov/ttn/atw/
aerosp/aeropg.html. Following
publication in the Federal Register, the
EPA will post the Federal Register
version of the proposal and key
technical documents at this same Web
site. Information on the overall residual
risk and technology review program is
available at the following Web site:
https://www.epa.gov/ttn/atw/rrisk/
rtrpg.html.
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C. What should I consider as I prepare
my comments for the EPA?
Submitting CBI. Do not submit
information containing CBI to the EPA
through https://www.regulations.gov or
email. Clearly mark the part or all of the
information that you claim to be CBI.
For CBI information on a disk or CD–
ROM that you mail to the 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
comments that includes information
claimed as CBI, you must submit a copy
of the comments that does not contain
the information claimed as CBI for
inclusion in the public docket. If you
submit a CD–ROM or disk that does not
contain CBI, 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 and the EPA’s electronic public
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docket without prior notice. Information
marked as CBI will not be disclosed
except in accordance with procedures
set forth in 40 Code of Federal
Regulations (CFR) part 2. Send or
deliver information identified as CBI
only to the following address: OAQPS
Document Control Officer (C404–02),
OAQPS, U.S. Environmental Protection
Agency, Research Triangle Park, North
Carolina 27711, Attention Docket ID No.
EPA–HQ–OAR–2014–0830.
II. Background
A. What is the statutory authority for
this action?
Section 112 of the CAA establishes a
two-stage regulatory process to address
emissions of HAP from stationary
sources. In the first stage, after the EPA
has identified categories of sources
emitting one or more of the HAP listed
in CAA section 112(b), CAA section
112(d) requires us to promulgate
technology-based NESHAP for those
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sources. ‘‘Major sources’’ are those that
emit or have the potential to emit 10
tons per year (tpy) or more of a single
HAP or 25 tpy or more of any
combination of HAP. For major sources,
the technology-based NESHAP must
reflect the maximum degree of emission
reductions of HAP achievable (after
considering cost, energy requirements
and non-air quality health and
environmental impacts) and are
commonly referred to as maximum
achievable control technology (MACT)
standards.
MACT standards must reflect the
maximum degree of emissions reduction
achievable through the application of
measures, processes, methods, systems
or techniques, including, but not limited
to, measures that: (1) Reduce the volume
of or eliminate pollutants through
process changes, substitution of
materials or other modifications; (2)
enclose systems or processes to
eliminate emissions; (3) capture or treat
pollutants when released from a
process, stack, storage or fugitive
emissions point; (4) are design,
equipment, work practice or operational
standards (including requirements for
operator training or certification); or (5)
are a combination of the above. CAA
section 112(d)(2)(A) through (E). The
MACT standards may take the form of
design, equipment, work practice or
operational standards where the EPA
first determines either that: (1) A
pollutant cannot be emitted through a
conveyance designed and constructed to
emit or capture the pollutant, or that
any requirement for or use of, such a
conveyance would be inconsistent with
law; or (2) the application of
measurement methodology to a
particular class of sources is not
practicable due to technological and
economic limitations. CAA section
112(h)(1) and (2).
The MACT ‘‘floor’’ is the minimum
control level allowed for MACT
standards promulgated under CAA
section 112(d)(3) and may not be based
on cost considerations. For new sources,
the MACT floor cannot be less stringent
than the emissions control that is
achieved in practice by the bestcontrolled similar source. The MACT
floor for existing sources can be less
stringent than floors for new sources,
but not less stringent than the average
emissions limitation achieved by the
best-performing 12 percent of existing
sources in the category or subcategory
(or the best-performing five sources for
categories or subcategories with fewer
than 30 sources). In developing MACT
standards, the EPA must also consider
control options that are more stringent
than the floor. We may establish
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standards more stringent than the floor
based on considerations of the cost of
achieving the emission reductions, any
non-air quality health and
environmental impacts and energy
requirements.
The EPA is then required to review
these technology-based standards and
revise them ‘‘as necessary (taking into
account developments in practices,
processes and control technologies)’’ no
less frequently than every 8 years. CAA
section 112(d)(6). In conducting this
review, the EPA is not required to
recalculate the MACT floor. Natural
Resources Defense Council (NRDC) v.
EPA, 529 F.3d 1077, 1084 (D.C. Cir.
2008). Association of Battery Recyclers,
Inc. v. EPA, 716 F.3d 667 (D.C. Cir.
2013).
The second stage in standard-setting
focuses on reducing any remaining (i.e.,
‘‘residual’’) risk according to CAA
section 112(f). CAA Section 112(f)(1)
required that the EPA prepare a report
to Congress discussing (among other
things) methods of calculating the risks
posed (or potentially posed) by sources
after implementation of the MACT
standards, the public health significance
of those risks and the EPA’s
recommendations as to legislation
regarding such remaining risk. The EPA
prepared and submitted the Residual
Risk Report to Congress, EPA–453/R–
99–001 (Risk Report) in March 1999.
CAA section 112(f)(2) then provides that
if Congress does not act on any
recommendation in the Risk Report, the
EPA must analyze and address residual
risk for each category or subcategory of
sources 8 years after promulgation of
such standards pursuant to CAA section
112(d).
Section 112(f)(2) of the CAA requires
the EPA to determine for source
categories subject to MACT standards
whether the emission standards provide
an ample margin of safety to protect
public health. Section 112(f)(2)(B) of the
CAA expressly preserves the EPA’s use
of the two-step process for developing
standards to address any residual risk
and the agency’s interpretation of
‘‘ample margin of safety’’ developed in
the National Emissions Standards for
Hazardous Air Pollutants: Benzene
Emissions from Maleic Anhydride
Plants, Ethylbenzene/Styrene Plants,
Benzene Storage Vessels, Benzene
Equipment Leaks, and Coke By-Product
Recovery Plants (Benzene NESHAP) (54
FR 38044, September 14, 1989). The
EPA notified Congress in the Risk
Report that the agency intended to use
the Benzene NESHAP approach in
making CAA section 112(f) residual risk
determinations (EPA–453/R–99–001, p.
ES–11). The EPA subsequently adopted
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8395
this approach in its residual risk
determinations and in a challenge to the
risk review for the Synthetic Organic
Chemical Manufacturing source
category, the United States Court of
Appeals for the District of Columbia
Circuit upheld as reasonable the EPA’s
interpretation that subsection 112(f)(2)
incorporates the approach established in
the Benzene NESHAP. See NRDC v.
EPA, 529 F.3d 1077, 1083 (D.C. Cir.
2008) (‘‘[S]ubsection 112(f)(2)(B)
expressly incorporates the EPA’s
interpretation of the Clean Air Act from
the Benzene standard, complete with a
citation to the Federal Register.’’); see
also A Legislative History of the Clean
Air Act Amendments of 1990, vol. 1, p.
877 (Senate debate on Conference
Report).
The first step in the process of
evaluating residual risk is the
determination of acceptable risk. If risks
are unacceptable, the EPA cannot
consider cost in identifying the
emissions standards necessary to bring
risks to an acceptable level. The second
step is the determination of whether
standards must be further revised in
order to provide an ample margin of
safety to protect public health. The
ample margin of safety is the level at
which the standards must be set, unless
an even more stringent standard is
necessary to prevent, taking into
consideration costs, energy, safety and
other relevant factors, an adverse
environmental effect.
1. Step 1—Determination of
Acceptability
The agency in the Benzene NESHAP
concluded that ‘‘the acceptability of risk
under section 112 is best judged on the
basis of a broad set of health risk
measures and information’’ and that the
‘‘judgment on acceptability cannot be
reduced to any single factor.’’ Benzene
NESHAP at 38046. The determination of
what represents an ‘‘acceptable’’ risk is
based on a judgment of ‘‘what risks are
acceptable in the world in which we
live’’ (Risk Report at 178, quoting NRDC
v. EPA, 824 F. 2d 1146, 1165 (D.C. Cir.
1987) (en banc) (‘‘Vinyl Chloride’’),
recognizing that our world is not riskfree.
In the Benzene NESHAP, we stated
that ‘‘EPA will generally presume that if
the risk to [the maximum exposed]
individual is no higher than
approximately one in 10 thousand, that
risk level is considered acceptable.’’ 54
FR 38045, September 14, 1989. We
discussed the maximum individual
lifetime cancer risk (or maximum
individual risk (MIR)) as being ‘‘the
estimated risk that a person living near
a plant would have if he or she were
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exposed to the maximum pollutant
concentrations for 70 years.’’ Id. We
explained that this measure of risk ‘‘is
an estimate of the upper bound of risk
based on conservative assumptions,
such as continuous exposure for 24
hours per day for 70 years.’’ Id. We
acknowledged that maximum
individual lifetime cancer risk ‘‘does not
necessarily reflect the true risk, but
displays a conservative risk level which
is an upper-bound that is unlikely to be
exceeded.’’ Id.
Understanding that there are both
benefits and limitations to using the
MIR as a metric for determining
acceptability, we acknowledged in the
Benzene NESHAP that ‘‘consideration of
maximum individual risk * * * must
take into account the strengths and
weaknesses of this measure of risk.’’ Id.
Consequently, the presumptive risk
level of 100-in-1 million (1-in-10
thousand) provides a benchmark for
judging the acceptability of maximum
individual lifetime cancer risk, but does
not constitute a rigid line for making
that determination. Further, in the
Benzene NESHAP, we noted that:
[p]articular attention will also be accorded to
the weight of evidence presented in the risk
assessment of potential carcinogenicity or
other health effects of a pollutant. While the
same numerical risk may be estimated for an
exposure to a pollutant judged to be a known
human carcinogen, and to a pollutant
considered a possible human carcinogen
based on limited animal test data, the same
weight cannot be accorded to both estimates.
In considering the potential public health
effects of the two pollutants, the Agency’s
judgment on acceptability, including the
MIR, will be influenced by the greater weight
of evidence for the known human
carcinogen.
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Id. at 38046. The agency also
explained in the Benzene NESHAP that:
[i]n establishing a presumption for MIR,
rather than a rigid line for acceptability, the
Agency intends to weigh it with a series of
other health measures and factors. These
include the overall incidence of cancer or
other serious health effects within the
exposed population, the numbers of persons
exposed within each individual lifetime risk
range and associated incidence within,
typically, a 50 km exposure radius around
facilities, the science policy assumptions and
estimation uncertainties associated with the
risk measures, weight of the scientific
evidence for human health effects, other
quantified or unquantified health effects,
effects due to co-location of facilities, and coemission of pollutants.
Id. at 38045. In some cases, these
health measures and factors taken
together may provide a more realistic
description of the magnitude of risk in
the exposed population than that
provided by maximum individual
lifetime cancer risk alone.
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As noted earlier, in NRDC v. EPA, the
court held that CAA section 112(f)(2)
‘‘incorporates the EPA’s interpretation
of the Clean Air Act from the Benzene
Standard.’’ The court further held that
Congress’ incorporation of the Benzene
standard applies equally to carcinogens
and non-carcinogens. 529 F.3d at 1081–
82. Accordingly, we also consider noncancer risk metrics in our determination
of risk acceptability and ample margin
of safety.
2. Step 2—Determination of Ample
Margin of Safety
CAA section 112(f)(2) requires the
EPA to determine, for source categories
subject to MACT standards, whether
those standards provide an ample
margin of safety to protect public health.
As explained in the Benzene NESHAP,
‘‘the second step of the inquiry,
determining an ‘ample margin of safety,’
again includes consideration of all of
the health factors, and whether to
reduce the risks even further . . .
Beyond that information, additional
factors relating to the appropriate level
of control will also be considered,
including costs and economic impacts
of controls, technological feasibility,
uncertainties and any other relevant
factors. Considering all of these factors,
the agency will establish the standard at
a level that provides an ample margin of
safety to protect the public health, as
required by section 112.’’ 54 FR 38046,
September 14, 1989.
According to CAA section
112(f)(2)(A), if the MACT standards for
HAP ‘‘classified as a known, probable,
or possible human carcinogen do not
reduce lifetime excess cancer risks to
the individual most exposed to
emissions from a source in the category
or subcategory to less than one in one
million,’’ the EPA must promulgate
residual risk standards for the source
category (or subcategory), as necessary
to provide an ample margin of safety to
protect public health. In doing so, the
EPA may adopt standards equal to
existing MACT standards if the EPA
determines that the existing standards
(i.e., the MACT standards) are
sufficiently protective. NRDC v. EPA,
529 F.3d 1077, 1083 (D.C. Cir. 2008) (‘‘If
EPA determines that the existing
technology-based standards provide an
‘ample margin of safety,’ then the
Agency is free to readopt those
standards during the residual risk
rulemaking.’’) The EPA must also adopt
more stringent standards, if necessary,
to prevent an adverse environmental
effect,1 but must consider cost, energy,
1 ‘‘Adverse environmental effect’’ is defined as
any significant and widespread adverse effect,
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safety and other relevant factors in
doing so.
The CAA does not specifically define
the terms ‘‘individual most exposed,’’
‘‘acceptable level’’ and ‘‘ample margin
of safety.’’ In the Benzene NESHAP, 54
FR 38044–38045, September 14, 1989,
we stated as an overall objective:
In protecting public health with an ample
margin of safety under section 112, EPA
strives to provide maximum feasible
protection against risks to health from
hazardous air pollutants by (1) protecting the
greatest number of persons possible to an
individual lifetime risk level no higher than
approximately 1-in-1 million and (2) limiting
to no higher than approximately 1-in-10
thousand [i.e., 100-in-1 million] the
estimated risk that a person living near a
plant would have if he or she were exposed
to the maximum pollutant concentrations for
70 years.
The agency further stated that ‘‘[t]he
EPA also considers incidence (the
number of persons estimated to suffer
cancer or other serious health effects as
a result of exposure to a pollutant) to be
an important measure of the health risk
to the exposed population. Incidence
measures the extent of health risks to
the exposed population as a whole, by
providing an estimate of the occurrence
of cancer or other serious health effects
in the exposed population.’’ Id. at
38045.
In the ample margin of safety decision
process, the agency again considers all
of the health risks and other health
information considered in the first step,
including the incremental risk reduction
associated with standards more
stringent than the MACT standard or a
more stringent standard that EPA has
determined is necessary to ensure risk is
acceptable. In the ample margin of
safety analysis, the agency considers
additional factors, including costs and
economic impacts of controls,
technological feasibility, uncertainties
and any other relevant factors.
Considering all of these factors, the
agency will establish the standard at a
level that provides an ample margin of
safety to protect the public health, as
required by CAA section 112(f). 54 FR
38046, September 14, 1989.
which may be reasonably anticipated to wildlife,
aquatic life or natural resources, including adverse
impacts on populations of endangered or threatened
species or significant degradation of environmental
qualities over broad areas. See CAA section
112(a)(7).
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B. What is this source category and how
does the current NESHAP regulate its
HAP emissions?
1. Description of the Aerospace
Manufacturing and Rework Facilities
Source Category and Applicability.
The NESHAP for the Aerospace
Manufacturing and Rework Facilities
source category (henceforth referred to
as the ‘‘Aerospace NESHAP’’) was
promulgated on September 1, 1995 (60
FR 45956) and codified at 40 CFR part
63, subpart GG. As promulgated in
1995, the Aerospace NESHAP applies to
the surface coating and related
operations at each new and existing
affected source of HAP emissions at
facilities that are major sources and are
engaged, either in part or in whole, in
the manufacture or rework of
commercial, civil or military aerospace
vehicles or components. The
requirements of the standards are nearly
the same for both new and existing
sources. The Aerospace NESHAP (40
CFR 63.742) defines ‘‘aerospace vehicle
or component’’ as ‘‘any fabricated part,
processed part, assembly of parts or
completed unit, with the exception of
electronic components, of any aircraft,
including, but not limited to airplanes,
helicopters, missiles, rockets, and space
vehicles.’’ Today, we estimate that 144
facilities are subject to the Aerospace
NESHAP. A complete list of facilities
subject to the Aerospace NESHAP is
available in the Aerospace RTR
database, which is available for review
in the docket for this proposed
rulemaking. Section 63.741(c) defines
each affected source in the Aerospace
Manufacturing and Rework Facilities
source category, and a facility could
have a combination of both new and
existing affected sources. However, the
emission standards for new and existing
affected sources are the same for nearly
all operations within subpart GG. The
exceptions are the filter efficiency
requirements to control inorganic HAP
emissions from primer and topcoat
spray application operations in 40 CFR
63.745 and for dry media blasting
operations in 40 CFR 63.746 and the
requirements for controls to reduce
organic HAP emissions from chemical
depainting operations in 40 CFR
63.746(c).
The Aerospace NESHAP applies to
organic HAP emissions from cleaning
operations, depainting operations,
primer application operations, topcoat
application operations, chemical milling
maskant application operations and the
handling and storage of waste. The rule
also applies to inorganic HAP emissions
from primer and topcoat application
operations using spray equipment and
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depainting operations using dry media
blasting. The rule provides an
exemption for primers, topcoats and
chemical milling maskants used in lowvolumes which is defined as 189 liters
(50 gallons) or less per formulation and
for which the combined annual total
does not exceed 757 liters (200 gallons).
The current Aerospace NESHAP
explicitly excludes specialty coatings
from meeting any control requirements,
as specified in 40 CFR 63.741(f) and in
40 CFR 63.742 (i.e., the definitions for
‘‘exterior primer,’’ ‘‘primer,’’ and
‘‘topcoat’’). Appendix A of the
Aerospace NESHAP defines 59 separate
categories of specialty coatings.
Although the EPA did not include
emission limitations for specialty
coatings in the Aerospace NESHAP
finalized in 1995 or in any subsequent
amendments, the EPA included VOC
content limits for the 59 categories of
specialty coatings in the 1997 Aerospace
Control Techniques Guidelines (CTG)
document.2 The CAA requires that state
implementation plans (SIPs) for certain
ozone nonattainment areas be revised to
require the implementation of
reasonably available control technology
(RACT) to control volatile organic
compounds (VOC) emissions. The EPA
has defined RACT as the lowest
emission limitation that a particular
source is capable of meeting by the
application of control technology that is
reasonably available considering
technological and economic feasibility.
The Aerospace CTG is intended to
provide state and local air pollution
control authorities with an information
base, recommended emissions
limitations and monitoring,
recordkeeping and reporting
requirements for proceeding with their
analyses of reasonably available control
technology (RACT) for their own
regulations to reduce VOC emissions
from aerospace surface coating
operations.
2. Organic and Inorganic HAP Emission
Sources
Organic HAP emissions from cleaning
and depainting operations occur from
the evaporation of the volatile portion of
the cleaning solvents or chemical
strippers. Cleaning emissions are
typically fugitive in nature and occur at
most processing steps. Emissions from
depainting operations that occur within
2 Guideline Series: Control of Volatile Organic
Compound Emissions from Coating Operations at
Aerospace Manufacturing and Rework Operations.
Emission Standards Division, U. S. Environmental
Protection Agency, Office of Air and Radiation,
Office of Air Quality Planning and Standards,
Research Triangle Park, NC 27711, December 1997.
Publication No. EPA–453/R–97–004.
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a booth or hangar are typically captured
and exhausted through a stack, although
some emissions may be fugitive in
nature (e.g., open tanks).
Organic HAP emissions from coating
(primers, topcoats and chemical milling
maskants) application operations occur
from the evaporation of the solvent
contained in the coatings. These
emissions occur during the application
of the coatings on aerospace vehicles or
parts, which may take place in large
open areas, such as hangars or in
partially or fully enclosed spaces, such
as within spray booths.
Organic HAP emissions from waste
occur from evaporation of the volatile
portion of the waste while it is being
handled or stored. These emissions are
fugitive in nature, occurring from each
waste container.
Some coatings contain compounds
that are inorganic HAP. Inorganic HAP
emissions from coatings occur during
the application of the coating if it is
applied using spray guns. These
inorganic HAP emissions are paint
particulates, commonly referred to as
‘‘overspray,’’ that do not adhere to the
surface being coated. Like the organic
HAP emissions from the operations, the
emissions of the inorganic HAP may
occur in large open areas, such as
hangars or in partially or fully enclosed
spaces, such as within spray booths.
However, coatings that contain
inorganic HAP are typically applied in
spray booths equipped with exhaust
filters to capture paint overspray.
Inorganic HAP are not emitted from
coatings applied with non-spray
methods, such as brushes, rollers or dip
coating, because the coating is not
atomized with these methods.
Inorganic HAP emissions from
depainting operations may occur from
non-chemical methods, such as plastic
and other types of dry media blasting,
used to strip an aerospace vehicle.
(Chemical stripping techniques do not
release inorganic HAP.) These emissions
occur as particulates generated during
the blasting process. The operation is
typically carried out within a large
hangar equipped with a ventilation
system and particulate filtration device
(e.g., a baghouse) or in smaller
enclosures, also equipped with
filtration. The inorganic HAP that are
released from the depainting operations
are primarily found in the paint being
stripped, although some stripping media
may contain trace amounts of inorganic
HAP.
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3. Regulation of Organic and Inorganic
HAP Emissions in the Aerospace
NESHAP
The Aerospace NESHAP specifies
numerical emission limits for organic
HAP emissions from primer, topcoat,
chemical milling maskant application
operations and chemical depainting
operations; equipment and filter
efficiency requirements for dry media
blasting depainting operations and
spray applied coating operations;
composition requirements and
equipment standards for cleaning
operations; and work practice standards
for waste handling and storage
operations.
The organic HAP emission rate for
primers is 540 grams/liter (g/L) (4.5
pounds/gallon (lb/gal)) (less water) for
general aviation rework facilities; 650 g/
L (5.4 lb/gal) (less water) for large
commercial aircraft; or 350 g/L (2.9 lb/
gal) for other primers (40 CFR
63.745(c)(1) and (2)). For topcoats and
self-priming topcoats the emission rate
is 420 g/L (3.5 lb/gal) (less water); and
540 g/L (4.5 lb/gal) (less water) for
primers and self-priming topcoats at
general aviation rework facilities (40
CFR 63.745(c)(3) and (4)). Alternatively,
a control system can be used to capture
and control emissions from the primer
or topcoat application operation (40
CFR 63.745(d)). The system must
achieve an overall control efficiency of
81 percent. Further, the Aerospace
NESHAP specifies which types of
coating application techniques may be
used (40 CFR 63.745(f)). The Aerospace
NESHAP also provides operating
requirements for the application of
primers or topcoats that contain
inorganic HAP, including control of
spray booth exhaust streams with either
particulate filters or waterwash systems
(40 CFR 63.745(g)). The primer and
topcoat limits and control requirements
do not apply to specialty coatings
defined in Appendix A to subpart GG.
The organic HAP emission content
limits for chemical milling maskants for
use with Type I chemical milling
solutions is 622 g/L (5.2 lb/gal) (less
water) and 160 g/L (1.3 lb/gal) (less
water) for use with Type II chemical
milling solutions (40 CFR 63.747(c)).
Alternatively, a control system that
achieves an overall control efficiency of
81 percent can be used to capture and
control emissions from the maskant
application operation (40 CFR
63.747(d)). These requirements do not
apply to touch-up of scratched surfaces
or damaged maskant and touch-up of
trimmed edges.
For cleaning operations (including
hand-wipe cleaning), the Aerospace
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NESHAP specifies that cleaning
solvents meet certain composition
requirements or that the cleaning
solvents have a composite vapor
pressure of no more than 45 millimeters
mercury (mm Hg) (24.1 in. water) (40
CFR 63.744(b)). Work practice measures
are also required (40 CFR 63.744(a)).
Four work practice alternative
techniques are specified for spray gun
cleaning, and work practice standards
are specified for flush cleaning
operations (40 CFR 63.744(c) and (d)).
The Aerospace NESHAP also specifies
requirements for depainting operations.
Where there are no controls for organic
HAP emissions from chemical
depainting operations, the rule prohibits
organic HAP emissions from chemical
depainting operations, with the
exception that 26 gallons of HAPcontaining chemical stripper (or
alternatively 190 pounds of organic
HAP) may be used for each commercial
aircraft stripped, or 50 gallons (or 365
pounds of organic HAP) for each
military aircraft for spot stripping and
decal removal (40 CFR 63.746(b)(1)
through (3)). Where there are controls
for organic HAP emissions from
chemical depainting, emissions must be
reduced by 81 percent for controls
installed before the effective date, and
by 95 percent for controls installed on
or after the effective date (40 CFR
63.746(c)). For non-chemical depainting
operations that generate inorganic HAP
emissions from dry media blasting, the
operation must be performed in an
enclosed area or in a closed cycle
depainting system and the air stream
from the operation must pass through a
dry filter system meeting a minimum
efficiency specified in the rule, through
a baghouse or through a waterwash
system before being released to the
atmosphere (40 CFR 63.746(b)(4)).
The handling and storage of waste
that contains HAP must be conducted in
a manner that minimizes spills (40 CFR
63.748).
C. What data collection activities were
conducted to support this action?
In February 2011, the EPA issued an
information collection request (ICR),
pursuant to CAA section 114, to
approximately 1,300 facilities that were
thought to potentially own and operate
Aerospace Manufacturing and Rework
Facilities. Information was requested on
operations subject to the Aerospace
NESHAP (coatings, blast depainting
operations, solvent depainting
operations and solvent cleaning
operations) as well as specialty coatings,
chemical milling and metal finishing
operations, composite processing,
storage tanks and wastewater treatment.
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Information was also requested on booth
characteristics and control devices and
location coordinates (latitude and
longitude) of emission stacks and
operations. The ICR requested available
information regarding coating and
solvent usage, process equipment,
control devices used, point and fugitive
HAP emissions, practices used to
control HAP emissions and other
aspects of facility operations. A total of
87 major source facilities and 57
synthetic minor facilities responded to
the survey and were included in the risk
modeling analysis. The remaining
facilities were either area source
facilities, not aerospace manufacturing
or rework facilities or closed facilities,
or the ICR was returned undeliverable.
We received data on coating and solvent
usage, chemical milling, metal finishing,
depainting operations, composite
processing operations, storage tanks,
wastewater treatment operations and
use of add-on control devices. From
these data, we were able to calculate
HAP emissions for each of the major
source and synthetic minor facilities
that responded to the survey.
In October 2012, the EPA issued a
request for stack test data under the
authority of section 114 of the CAA.
This request was sent to 9 parent
companies for 18 facilities, requesting
stack emissions testing data for selected
coating operations and spray booths and
blast depainting, composite processing
and metal finishing operations believed
to represent the various processes and
capture and control configurations used
by the industry. All facilities either
responded to the survey or provided
information indicating the operations
for which we requested stack testing
had been shutdown.
In September 2013, the EPA issued an
additional request to the same
companies requesting supplemental
testing to confirm the content of the
coatings used in the October 2012 stack
testing. These data were used to speciate
emissions for individual coatings and to
develop the default chromium
speciation profile for processes included
in the 2011 ICR.
In May 2014, the EPA solicited
industry review of the EPA’s draft
modeling file records (e.g., estimated
emissions and emission estimation
methods) that were developed based on
the results of the data collection efforts
described above and the 2011 National
Emission Inventory (NEI) and 2005
National Air Toxics Assessment (NATA)
discussed in section II.D of this
preamble. Of the 171 facilities
contacted, 84 facilities responded. Of
the 171 facilities contacted, the EPA
determined that 144 are in operation
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and subject to the NESHAP and 27
facilities are closed or not subject to the
Aerospace NESHAP (e.g., are area
sources). The 144 facilities that were
determined to be in operation and
subject to the NESHAP are included in
the model input file for the risk
assessment.
D. What other relevant background
information and data are available?
The 2011 NEI provided supplemental
information for this RTR. The NEI is a
database that contains information
about sources that emit criteria air
pollutants, their precursors and HAP.
The database includes estimates of
annual air pollutant emissions from
point, nonpoint and mobile sources in
the 50 states, the District of Columbia,
Puerto Rico and the Virgin Islands. The
EPA collects this information and
releases an updated version of the NEI
database every 3 years. The NEI
includes information necessary for
conducting risk modeling, including
annual HAP emissions estimates from
individual emission points at facilities
and the related emissions release
parameters. For each emission record
that was needed for the model input file
for the risk assessment (hereafter
referred to as the ‘‘RTR emissions
dataset’’) that was not available from the
2011 ICR responses, the EPA used
available data in the 2011 NEI as the
first alternative. The NEI emission
records used included annual HAP
emissions estimates for boilers, engines,
chemical manufacturing processes,
secondary metal production processes,
heaters, soil remediation, transportation
equipment, waste disposal, welding and
other miscellaneous manufacturing
processes that were not included in the
2011 ICR. Individual chromium
emissions estimates were excluded from
the modeling file if they were found to
overlap with a regulated process.
The 2005 NATA also provided
supplemental data for the RTR
emissions dataset for this RTR. The
2005 NATA includes annual HAP
emissions estimates for three Aerospace
Manufacturing and Rework Facilities
that are not in the 2011 NEI. These data
were incorporated into the RTR
emissions dataset, and include emission
data for space heaters, boilers and
underground fuel tanks at the facilities.
Although the 2005 NATA data is
outdated, we thought it important to
ensure we had accounted for all the
major sources in the source category and
given that we did not have data on three
of the facilities, EPA augmented our
RTR emissions dataset with this data for
three of the 144 facilities. We expect to
have updated NATA soon and will
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consider the impact on the three
sources, as appropriate. NATA is the
EPA’s ongoing evaluation of air toxics in
the United States. The EPA developed
NATA as a screening tool for state/local/
tribal agencies to prioritize pollutants,
emission sources and locations of
interest for further study in order to gain
a better understanding of population
risks. NATA assessments do not
incorporate refined information about
emission sources, but rather use general
information about sources to develop
estimates of risks which are more likely
to overestimate impacts than
underestimate them. NATA provides
estimates of the risk of cancer and other
serious health effects from breathing
(inhaling) air toxics in order to inform
both national and more localized efforts
to identify and prioritize air toxics,
emission source types and locations
which are of greatest potential concern
in terms of contributing to population
risk.
E. What litigation is related to this
proposed action?
In 2007, the United States Court of
Appeals for the District of Columbia
Circuit found that the EPA had erred in
establishing emissions standards for
sources of HAP in the NESHAP for
Brick and Structural Clay Products
Manufacturing and Clay Ceramics
Manufacturing, 67 FR 26690 (May 16,
2003), and consequently vacated the
rules.3 Among other things, the court
found EPA erred by failing to regulate
processes that emitted HAP, in some
instances by establishing a MACT floor
of ‘‘no control.’’ In this action we are
proposing to correct the same error in
the Aerospace NESHAP by proposing to
remove the exemption for specialty
coatings found at 40 CFR 63.741(f) and
instead add limits for specialty coatings
(including adhesives, adhesive bonding
primers and sealants).
In a separate case, the court vacated
portions of two provisions in the EPA’s
CAA section 112 regulations that govern
emissions of HAP during periods of
SSM.4 Specifically, the court vacated
the SSM exemption contained in 40
CFR 63.6(f)(1) and 40 CFR 63.6(h)(1),
holding that under section 302(k) of the
CAA, emissions standards or limitations
must be continuous in nature and that
the SSM exemption violates the CAA’s
requirement that some section 112
standards apply continuously. In this
action, we are also proposing to revise
these provisions for Aerospace
3 Sierra
Club v. EPA, 479 F. 3d 875 (D.C. Cir.
March 13, 2007).
4 Sierra Club v. EPA, 551 F. 3d 1019 (D.C. Cir.
2008), cert. denied, 130 S. Ct 1735 (2010).
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Manufacturing and Rework Facilities
operations, as discussed in section
IV.E.2 of this preamble.
III. Analytical Procedures
In this section, we describe the
analyses performed to support the
proposed decisions for the RTR and
other issues addressed in this proposal.
A. How did we estimate post-MACT
risks posed by the source category?
The EPA conducted a risk assessment
that provides estimates of the MIR
posed by the HAP emissions from each
source in the source category, the
hazard index (HI) for chronic exposures
to HAP with the potential to cause noncancer health effects and the hazard
quotient (HQ) for acute exposures to
HAP with the potential to cause noncancer health effects. The assessment
also provides estimates of the
distribution of cancer risks within the
exposed populations, cancer incidence
and an evaluation of the potential for
adverse environmental effects. The
seven sections that follow this
paragraph describe how we estimated
emissions and conducted the risk
assessment. The docket for this
rulemaking contains the following
document that provides more
information on the risk assessment
inputs and models: Residual Risk
Assessment for the Aerospace
Manufacturing and Rework Facilities
Source Category in Support of the
January, 2015 Risk and Technology
Review Proposal, January 2015. The
methods used to assess risks (as
described in the primary steps below)
are consistent with those peer-reviewed
by a panel of the EPA’s Science
Advisory Board (SAB) in 2009 and
described in their peer review report
issued in 2010;5 they are also consistent
with the key recommendations
contained in that report.
1. How did we estimate actual
emissions and identify the emissions
release characteristics?
Data for 144 Aerospace Manufacturing
and Rework Facilities were used to
create the RTR emissions dataset, as
described in section II.C of this
preamble. The emissions sources
included in the RTR emissions dataset
includes the following types of sources
currently regulated by the Aerospace
NESHAP: Primer/topcoat application
operations, waste handling operations,
chemical milling maskant application
5 U.S. EPA SAB. Risk and Technology Review
(RTR) Risk Assessment Methodologies: For Review
by the EPA’s Science Advisory Board with Case
Studies—MACT I Petroleum Refining Sources and
Portland Cement Manufacturing, May 2010.
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operations, cleaning operations and
chemical and blast depainting
operations. The RTR emissions dataset
also includes the following types of
sources not currently regulated by the
Aerospace NESHAP: Specialty coatings,
composite processing, chemical milling
and metal finishing, wastewater, storage
tanks, boilers, engines, chemical
manufacturing processes, secondary
metal production processes, heaters, soil
remediation, transportation equipment,
waste disposal, welding and other
miscellaneous manufacturing processes.
These emission sources include both
fugitive emissions and stack emissions.
This RTR emissions dataset is based
primarily on data gathered through the
CAA section 114 questionnaire, as
described in section II.C of this
preamble. This dataset was
supplemented with data received from
the 2012 ICR for stack testing data and
the 2013 request for information on
coatings analyses (as described in
section II.C of this preamble), the 2011
NEI (as described in section II.D of this
preamble) and the 2005 NATA (as
described in section II.D of this
preamble). The sources noted above
provided all of the emissions data in the
RTR emissions dataset and nearly all of
the facility specific data needed to
conduct the risk modeling analysis.
However, there were limited instances
where default values were used to fill
gaps in the facility-specific data used in
the risk modeling analysis. Examples of
default values used to fill these data
gaps were default values used for stack
height and other release point
parameters, and percentages used to
segregate mercury and chromium
compounds into separate species. Use of
defaults is discussed in detail in the
memorandum, Aerospace
Manufacturing and Rework Facilities
RTR Modeling File Preparation,
December 2014, available in the docket
for this action (Modeling File
Preparation Memo).
The RTR emissions dataset was
refined following an extensive quality
assurance check of source locations,
emission release characteristics and
annual emission estimates. We checked
the coordinates of each emission source
in the dataset using ArcGIS to ensure
the emission point locations were
correct. Also, as discussed in section
II.C of this preamble, in May 2014, the
EPA solicited industry review of the
dataset and made corrections, as
needed. For further information on the
EPA’s quality assurance review, see the
Modeling File Preparation Memo
available in the docket for this action.
A list of the 144 facilities and
additional information used to develop
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the RTR emissions dataset is available
in the Aerospace RTR database, and
documentation on the development of
this database is provided in the
Modeling File Preparation Memo, both
of which are available in the docket for
this action.
2. How did we estimate MACTallowable emissions?
The available emissions data in the
RTR emissions dataset include estimates
of the actual mass of HAP emitted
during the specified annual time period.
In some cases, these ‘‘actual’’ emission
levels are lower than the emission levels
required to comply with the MACT
standards. The emissions level allowed
to be emitted by the MACT standards is
referred to as the ‘‘MACT-allowable’’
emissions level. We discussed the use of
both MACT-allowable and actual
emissions in the final Coke Oven
Batteries residual risk rule (70 FR
19998–19999, April 15, 2005) and in the
proposed and final Hazardous Organic
NESHAP residual risk rules (71 FR
34428, June 14, 2006 and 71 FR 76609,
December 21, 2006, respectively). In
those previous actions, we noted that
assessing the risks at the MACTallowable level is inherently reasonable
since these risks reflect the maximum
level facilities could emit and still
comply with national emission
standards. We also explained that it is
reasonable to consider actual emissions,
where such data are available, in both
steps of the risk analysis, in accordance
with the Benzene NESHAP approach.
(54 FR 38044, September 14, 1989.)
We used the RTR emissions dataset
discussed in section III.A.1 of this
preamble to estimate MACT-allowable
emissions levels. Facilities were asked
to provide a multiplier in the 2011 ICR
survey to scale up average hourly
emissions to maximum hourly
emissions for air dispersion modeling,
given that each facility typically has a
large number of emission points and it
would be difficult to determine the
maximum hourly emissions from each
emission point. Many of the facilities
reported multipliers that were based on,
for example, scaling production from
2,000 hours to 8,760 hours per year or
from one shift per day to three shifts.
However, using these values would
have led to unrealistically high
‘‘allowable’’ emission values because of
limitations in the market for new
aerospace vehicles and for rework
services, and because many facilities
have permit restrictions on their total
annual emissions. Therefore, the EPA
did not use maximum hourly emissions
and instead chose to use a multiplier
based on current and historical industry
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capacity utilization factors. The EPA
chose to use a single multiplier of 1.02
to scale average annual emissions to
allowable annual emissions. The
allowable emissions multiplier is based
on the difference between 2008
production utilization rate of 83.1
percent and the 20-year historical
maximum production utilization rate
from 1990 of 85.0 percent (85 ÷ 83.1 =
1.02). The docket for this rulemaking
contains information on the
development of estimated MACTallowable emissions in the Modeling
File Preparation Memo.
3. How did we conduct dispersion
modeling, determine inhalation
exposures and estimate individual and
population inhalation risks?
Both long-term and short-term
inhalation exposure concentrations and
health risks from the source category
addressed in this proposal were
estimated using the Human Exposure
Model (Community and Sector HEM–3
version 1.1.0). The HEM–3 performs
three primary risk assessment activities:
(1) Conducting dispersion modeling to
estimate the concentrations of HAP in
ambient air, (2) estimating long-term
and short-term inhalation exposures to
individuals residing within 50
kilometers (km) of the modeled
sources 6 and (3) estimating individual
and population-level inhalation risks
using the exposure estimates and
quantitative dose-response information.
The air dispersion model used in the
analysis, the AERMOD model, is one of
the EPA’s preferred models for assessing
pollutant concentrations from industrial
facilities.7 To perform the dispersion
modeling and to develop the
preliminary risk estimates, HEM–3
draws on three data libraries. The first
is a library of meteorological data,
which is used for dispersion
calculations. This library includes 1
year (2011) of hourly surface and upper
air observations for more than 800
meteorological stations, selected to
provide coverage of the United States
and Puerto Rico. A second library of
United States Census Bureau census
block 8 internal point locations and
populations provides the basis of
human exposure calculations (U.S.
Census, 2010). In addition, for each
census block, the census library
6 This metric comes from the Benzene NESHAP.
See 54 FR 38046.
7 U.S. EPA. Revision to the Guideline on Air
Quality Models: Adoption of a Preferred General
Purpose (Flat and Complex Terrain) Dispersion
Model and Other Revisions (70 FR 68218,
November 9, 2005).
8 A census block is the smallest geographic area
for which census statistics are tabulated.
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includes the elevation and controlling
hill height, which are also used in
dispersion calculations. A third library
of pollutant unit risk factors and other
health benchmarks is used to estimate
health risks. These risk factors and
health benchmarks are the latest values
recommended by the EPA for HAP and
other toxic air pollutants. These values
are available at: https://www.epa.gov/ttn/
atw/toxsource/summary.html and are
discussed in more detail later in this
section.
In developing the risk assessment for
chronic exposures, we used the
estimated annual average ambient air
concentrations of each HAP emitted by
each source for which we have
emissions data in the source category.
The air concentrations at each nearby
census block centroid were used as a
surrogate for the chronic inhalation
exposure concentration for all the
people who reside in that census block.
We calculated the MIR for each facility
as the cancer risk associated with a
continuous lifetime (24 hours per day,
7 days per week and 52 weeks per year
for a 70-year period) exposure to the
maximum concentration at the centroid
of inhabited census blocks. Individual
cancer risks were calculated by
multiplying the estimated lifetime
exposure to the ambient concentration
of each of the HAP (in micrograms per
cubic meter (mg/m3)) by its unit risk
estimate (URE). The URE is an upper
bound estimate of an individual’s
probability of contracting cancer over a
lifetime of exposure to a concentration
of 1 microgram of the pollutant per
cubic meter of air. For residual risk
assessments, we generally use URE
values from the EPA’s Integrated Risk
Information System (IRIS). For
carcinogenic pollutants without IRIS
values, we look to other reputable
sources of cancer dose-response values,
often using California EPA (CalEPA)
URE values, where available. In cases
where new, scientifically credible dose
response values have been developed in
a manner consistent with the EPA
guidelines and have undergone a peer
review process similar to that used by
the EPA, we may use such doseresponse values in place of, or in
addition to, other values, if appropriate.
The EPA estimated incremental
individual lifetime cancer risks
associated with emissions from the
facilities in the source category as the
sum of the risks for each of the
carcinogenic HAP (including those
classified as carcinogenic to humans,
likely to be carcinogenic to humans and
suggestive evidence of carcinogenic
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potential 9) emitted by the modeled
sources. Cancer incidence and the
distribution of individual cancer risks
for the population within 50 km of the
sources were also estimated for the
source category as part of this
assessment by summing individual
risks. A distance of 50 km is consistent
with both the analysis supporting the
1989 Benzene NESHAP (54 FR 38044,
September 14, 1989) and the limitations
of Gaussian dispersion models,
including AERMOD.
To assess the risk of non-cancer
health effects from chronic exposures,
we summed the HQ for each of the HAP
that affects a common target organ
system to obtain the HI for that target
organ system (or target organ-specific
HI, TOSHI). The HQ is the estimated
exposure divided by the chronic
reference value, which is a value
selected from one of several sources.
First, the chronic reference level can be
the EPA reference concentration (RfC)
(https://www.epa.gov/riskassessment/
glossary.htm), defined as ‘‘an estimate
(with uncertainty spanning perhaps an
order of magnitude) of a continuous
inhalation exposure to the human
population (including sensitive
subgroups) that is likely to be without
an appreciable risk of deleterious effects
during a lifetime.’’ Alternatively, in
cases where an RfC from the EPA’s IRIS
database is not available or where the
EPA determines that using a value other
than the RfC is appropriate, the chronic
reference level can be a value from the
following prioritized sources: (1) The
Agency for Toxic Substances and
Disease Registry (ATSDR) Minimum
Risk Level (https://www.atsdr.cdc.gov/
mrls/index.asp), which is defined as ‘‘an
estimate of daily human exposure to a
hazardous substance that is likely to be
without an appreciable risk of adverse
non-cancer health effects (other than
cancer) over a specified duration of
exposure’’; (2) the CalEPA Chronic
Reference Exposure Level (REL)
(https://www.oehha.ca.gov/air/hot_
spots/pdf/HRAguidefinal.pdf), which is
defined as ‘‘the concentration level (that
is expressed in units of micrograms per
cubic meter (mg/m3) for inhalation
9 These classifications also coincide with the
terms ‘‘known carcinogen, probable carcinogen, and
possible carcinogen,’’ respectively, which are the
terms advocated in the EPA’s previous Guidelines
for Carcinogen Risk Assessment, published in 1986
(51 FR 33992, September 24, 1986). Summing the
risks of these individual compounds to obtain the
cumulative cancer risks is an approach that was
recommended by the EPA’s SAB in their 2002 peer
review of EPA’s NATA entitled, NATA—Evaluating
the National-scale Air Toxics Assessment 1996
Data—an SAB Advisory, available at: https://
yosemite.epa.gov/sab/sabproduct.nsf/
214C6E915BB04E14852570CA007A682C/$File/
ecadv02001.pdf.
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exposure and in a dose expressed in
units of milligram per kilogram-day for
oral exposures), at or below which no
adverse health effects are anticipated for
a specified exposure duration’’; or (3), as
noted above, a scientifically credible
dose-response value that has been
developed in a manner consistent with
the EPA guidelines and has undergone
a peer review process similar to that
used by the EPA, in place of or in
concert with other values.
As mentioned above, in order to
characterize non-cancer chronic effects,
and in response to key
recommendations from the SAB, the
EPA selects dose-response values that
reflect the best available science for all
HAP included in RTR risk
assessments.10 More specifically, for a
given HAP, the EPA examines the
availability of inhalation reference
values from the sources included in our
tiered approach (e.g., IRIS first, ATSDR
second, CalEPA third) and determines
which inhalation reference value
represents the best available science.
Thus, as new inhalation reference
values become available, the EPA will
typically evaluate them and determine
whether they should be given
preference over those currently being
used in RTR risk assessments.
The EPA also evaluated screening
estimates of acute exposures and risks
for each of the HAP at the point of
highest potential off-site exposure for
each facility. To do this, the EPA
estimated the risks when both the peak
hourly emissions rate and worst-case
dispersion conditions occur. We also
assume that a person is located at the
point of highest impact during that same
time. In accordance with our mandate in
section 112 of the CAA, we use the
point of highest off-site exposure to
assess the potential risk to the
maximally exposed individual. The
acute HQ is the estimated acute
exposure divided by the acute doseresponse value. In each case, the EPA
calculated acute HQ values using best
available, short-term dose-response
values. These acute dose-response
values, which are described below,
include the acute REL, acute exposure
guideline levels (AEGL) and emergency
response planning guidelines (ERPG) for
1-hour exposure durations. As
discussed below, we used conservative
assumptions for emissions rates,
meteorology and exposure location for
our acute analysis.
10 The SAB peer review of RTR Risk Assessment
Methodologies is available at: https://
yosemite.epa.gov/sab/sabproduct.nsf/
4AB3966E263D943A8525771F00668381/$File/EPASAB-10-007-unsigned.pdf.
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As described in the CalEPA’s Air
Toxics Hot Spots Program Risk
Assessment Guidelines, Part I, The
Determination of Acute Reference
Exposure Levels for Airborne Toxicants,
an acute REL value (https://
www.oehha.ca.gov/air/pdf/acuterel.pdf)
is defined as ‘‘the concentration level at
or below which no adverse health
effects are anticipated for a specified
exposure duration.’’ Id. at page 2. Acute
REL values are based on the most
sensitive, relevant, adverse health effect
reported in the peer-reviewed medical
and toxicological literature. Acute REL
values are designed to protect the most
sensitive individuals in the population
through the inclusion of margins of
safety. Because margins of safety are
incorporated to address data gaps and
uncertainties, exceeding the REL does
not automatically indicate an adverse
health impact.
AEGL values were derived in
response to recommendations from the
National Research Council (NRC). As
described in Standing Operating
Procedures (SOP) of the National
Advisory Committee on Acute Exposure
Guideline Levels for Hazardous
Substances (https://www.epa.gov/oppt/
aegl/pubs/sop.pdf),11 ‘‘the NRC’s
previous name for acute exposure
levels—community emergency exposure
levels—was replaced by the term AEGL
to reflect the broad application of these
values to planning, response and
prevention in the community, the
workplace, transportation, the military
and the remediation of Superfund
sites.’’ Id. at 2. This document also
states that AEGL values ‘‘represent
threshold exposure limits for the general
public and are applicable to emergency
exposures ranging from 10 minutes to
eight hours.’’ Id. at 2.
The document lays out the purpose
and objectives of AEGL by stating that
‘‘the primary purpose of the AEGL
program and the National Advisory
Committee for Acute Exposure
Guideline Levels for Hazardous
Substances is to develop guideline
levels for once-in-a-lifetime, short-term
exposures to airborne concentrations of
acutely toxic, high-priority chemicals.’’
Id. at 21. In detailing the intended
application of AEGL values, the
document states that ‘‘[i]t is anticipated
that the AEGL values will be used for
regulatory and nonregulatory purposes
by U.S. federal and state agencies and
possibly the international community in
conjunction with chemical emergency
11 National Academy of Sciences (NAS), 2001.
Standing Operating Procedures for Developing
Acute Exposure Levels for Hazardous Chemicals,
page 2.
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response, planning and prevention
programs. More specifically, the AEGL
values will be used for conducting
various risk assessments to aid in the
development of emergency
preparedness and prevention plans, as
well as real-time emergency response
actions, for accidental chemical releases
at fixed facilities and from transport
carriers.’’ Id. at 31.
The AEGL–1 value is then specifically
defined as ‘‘the airborne concentration
(expressed as ppm (parts per million) or
mg/m3 (milligrams per cubic meter)) of
a substance above which it is predicted
that the general population, including
susceptible individuals, could
experience notable discomfort,
irritation, or certain asymptomatic
nonsensory effects. However, the effects
are not disabling and are transient and
reversible upon cessation of exposure.’’
Id. at 3. The document also notes that,
‘‘Airborne concentrations below AEGL–
1 represent exposure levels that can
produce mild and progressively
increasing but transient and
nondisabling odor, taste, and sensory
irritation or certain asymptomatic,
nonsensory effects.’’ Id. Similarly, the
document defines AEGL–2 values as
‘‘the airborne concentration (expressed
as parts per million or milligrams per
cubic meter) of a substance above which
it is predicted that the general
population, including susceptible
individuals, could experience
irreversible or other serious, long-lasting
adverse health effects or an impaired
ability to escape.’’ Id.
ERPG values are derived for use in
emergency response, as described in the
American Industrial Hygiene
Association’s Emergency Response
Planning Committee document titled,
ERPGS Procedures and Responsibilities
(https://sp4m.aiha.org/insideaiha/
GuidelineDevelopment/ERPG/
Documents/ERP-SOPs2006.pdf), which
states that, ‘‘Emergency Response
Planning Guidelines were developed for
emergency planning and are intended as
health based guideline concentrations
for single exposures to chemicals.’’ 12 Id.
at 1. The ERPG–1 value is defined as
‘‘the maximum airborne concentration
below which it is believed that nearly
all individuals could be exposed for up
to 1 hour without experiencing other
than mild transient adverse health
effects or without perceiving a clearly
defined, objectionable odor.’’ Id. at 2.
Similarly, the ERPG–2 value is defined
as ‘‘the maximum airborne
concentration below which it is
believed that nearly all individuals
could be exposed for up to one hour
without experiencing or developing
irreversible or other serious health
effects or symptoms which could impair
an individual’s ability to take protective
action.’’ Id. at 1.
As can be seen from the definitions
above, the AEGL and ERPG values
include the similarly defined severity
levels 1 and 2. For many chemicals, a
severity level 1 value AEGL or ERPG has
not been developed because the types of
effects for these chemicals are not
consistent with the AEGL–1/ERPG–1
definitions; in these instances, we
compare higher severity level AEGL–2
or ERPG–2 values to our modeled
exposure levels to screen for potential
acute concerns. When AEGL–1/ERPG–1
values are available, they are used in
our acute risk assessments.
Acute REL values for 1-hour exposure
durations are typically lower than their
corresponding AEGL–1 and ERPG–1
values. Even though their definitions are
slightly different, AEGL–1 values are
often the same as the corresponding
ERPG–1 values, and AEGL–2 values are
often equal to ERPG–2 values.
Maximum HQ values from our acute
screening risk assessments typically
result when basing them on the acute
REL value for a particular pollutant. In
cases where our maximum acute HQ
value exceeds 1, we also report the HQ
value based on the next highest acute
dose-response value (usually the AEGL–
1 and/or the ERPG–1 value).
To develop screening estimates of
acute exposures in the absence of hourly
emissions data, generally we first
develop estimates of maximum hourly
emissions rates by multiplying the
average actual annual hourly emissions
rates by a default factor to cover
routinely variable emissions. We choose
the factor to use partially based on
process knowledge and engineering
judgment. The factor chosen also
reflects a Texas study of short-term
emissions variability, which showed
that most peak emission events in a
heavily-industrialized four-county area
(Harris, Galveston, Chambers and
Brazoria Counties, Texas) were less than
twice the annual average hourly
emissions rate. The highest peak
emissions event was 74 times the
annual average hourly emissions rate,
and the 99th percentile ratio of peak
hourly emissions rate to the annual
average hourly emissions rate was 9.13
Considering this analysis, to account for
more than 99 percent of the peak hourly
12 ERP Committee Procedures and
Responsibilities. November 1, 2006. American
Industrial Hygiene Association.
13 See https://www.tceq.state.tx.us/compliance/
field_ops/eer/ or the docket to access the
source of these data.
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emissions, we apply a conservative
screening multiplication factor of 10 to
the average annual hourly emissions
rate in our acute exposure screening
assessments as our default approach.
However, we use a factor other than 10
if we have information that indicates
that a different factor is appropriate for
a particular source category.
For this source category, the default
value was not utilized. A peak 1-hour
emission multiplier of 1.2 times the
annual emissions was utilized for the
entire source category. This value was
developed from current and historical
industry capacity utilization factors.
The emissions from this category are
generally dependent on the amount of
HAP in the coatings and the amount of
coating applied, and would only vary in
a significant manner if production
increased. Therefore, the EPA based the
acute emissions multiplier on potential
changes in production. The acute
emissions multiplier is based on the
difference between 2008 production
utilization rate of 83.1 percent and the
maximum production utilization rate of
100 percent, which has not been
realized in 20 years of historical data
(100 ÷ 83.1 = 1.2). The docket for this
rulemaking contains information on the
development of estimated MACT-acute
emissions in the Modeling File
Preparation Memo. A further discussion
of why this factor was chosen can be
found in Appendix 1 of the Modeling
File Preparation Memo, available in the
docket for this rulemaking.
As part of our acute risk assessment
process, for cases where acute HQ
values from the screening step were less
than or equal to 1 (even under the
conservative assumptions of the
screening analysis), acute impacts were
deemed negligible and no further
analysis was performed. In cases where
an acute HQ from the screening step
was greater than 1, additional sitespecific data were considered to
develop a more refined estimate of the
potential for acute impacts of concern.
For this source category, the data
refinements employed consisted of
evaluating the off-site extent of any
exceedances of the acute health
benchmarks. These refinements are
discussed more fully in the Modeling
File Preparation Memo, which is
available in the docket for this source
category. Ideally, we would prefer to
have continuous measurements over
time to see how the emissions vary by
each hour over an entire year. Having a
frequency distribution of hourly
emissions rates over a year would allow
us to perform a probabilistic analysis to
estimate potential threshold
exceedances and their frequency of
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occurrence. Such an evaluation could
include a more complete statistical
treatment of the key parameters and
elements adopted in this screening
analysis. Recognizing that this level of
data is rarely available, we instead rely
on the multiplier approach.
To better characterize the potential
health risks associated with estimated
acute exposures to HAP, and in
response to a key recommendation from
the SAB’s peer review of the EPA’s RTR
risk assessment methodologies,14 we
generally examine a wider range of
available acute health metrics (e.g.,
RELs, AEGLs) than we do for our
chronic risk assessments. This is in
response to the SAB’s acknowledgement
that there are generally more data gaps
and inconsistencies in acute reference
values than there are in chronic
reference values. In some cases, when
Reference Value Arrays 15 for HAP have
been developed, we consider additional
acute values (i.e., occupational and
international values) to provide a more
complete risk characterization.
4. How did we conduct the
multipathway exposure and risk
screening?
The EPA conducted a screening
analysis examining the potential for
significant human health risks due to
exposures via routes other than
inhalation (i.e., ingestion). We first
determined whether any sources in the
Aerospace Manufacturing and Rework
Facilities source category emitted any
HAP known to be persistent and
bioaccumulative in the environment
(PB–HAP). The PB–HAP compounds or
compound classes are identified for the
screening from the EPA’s Air Toxics
Risk Assessment Library (available at
https://www2.epa.gov/fera/riskassessment-and-modeling-air-toxicsrisk-assessment-reference-library).
For the Aerospace Manufacturing and
Rework Facilities source category, we
identified emissions of cadmium,
dioxins/furans, POM, mercury (both
inorganic mercury and methyl mercury)
and lead compounds. Because one or
more of these PB–HAP are emitted by at
least one facility in the Aerospace
Manufacturing and Rework Facilities
14 The SAB peer review of RTR Risk Assessment
Methodologies is available at: https://
yosemite.epa.gov/sab/sabproduct.nsf/
4AB3966E263D943A8525771F00668381/$File/EPASAB-10-007-unsigned.pdf.
15 U.S. EPA. (2009) Chapter 2.9, Chemical
Specific Reference Values for Formaldehyde, in
Graphical Arrays of Chemical-Specific Health Effect
Reference Values for Inhalation Exposures (Final
Report). U.S. Environmental Protection Agency,
Washington, DC, EPA/600/R–09/061, and available
online at https://cfpub.epa.gov/ncea/cfm/
recordisplay.cfm?deid=211003.
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source category, we proceeded to the
next step of the evaluation. In this step,
we determined whether the facilityspecific emissions rates of the emitted
PB–HAP were large enough to create the
potential for significant non-inhalation
human health risks under reasonable
worst-case conditions. To facilitate this
step, we developed emissions rate
screening levels for several PB–HAP
using a hypothetical upper-end
screening exposure scenario developed
for use in conjunction with the EPA’s
Total Risk Integrated Methodology.Fate,
Transport, and Ecological Exposure
(TRIM.FaTE) model. The PB–HAP with
emissions rate screening levels are:
Lead, cadmium, chlorinated
dibenzodioxins and furans, mercury
compounds and POM. We conducted a
sensitivity analysis on the screening
scenario to ensure that its key design
parameters would represent the upper
end of the range of possible values, such
that it would represent a conservative,
but not impossible scenario. The
facility-specific emissions rates of these
PB–HAP were compared to the emission
rate screening levels for these PB–HAP
to assess the potential for significant
human health risks via non-inhalation
pathways. We call this application of
the TRIM.FaTE model the Tier 1 TRIMscreen or Tier 1 screen.
For the purpose of developing
emissions rates for our Tier 1 TRIMscreen, we derived emission levels for
these PB–HAP (other than lead
compounds) at which the maximum
excess lifetime cancer risk would be 1in-1 million (i.e., for polychlorinated
dibenzodioxins and furans and POM)
or, for HAP that cause non-cancer health
effects (i.e., cadmium compounds and
mercury compounds), the maximum HQ
would be 1. If the emissions rate of any
PB–HAP included in the Tier 1 screen
exceeds the Tier 1 screening emissions
rate for any facility, we conduct a
second screen, which we call the Tier 2
TRIM-screen or Tier 2 screen.
In the Tier 2 screen, the location of
each facility that exceeded the Tier 1
emission rate is used to refine the
assumptions associated with the
environmental scenario while
maintaining the exposure scenario
assumptions. A key assumption that is
part of the Tier 1 screen is that a lake
is located near the facility; we confirm
the existence of lakes near the facility as
part of the Tier 2 screen. We then adjust
the risk-based Tier 1 screening level for
each PB–HAP for each facility based on
an understanding of how exposure
concentrations estimated for the
screening scenario change with
meteorology and environmental
assumptions. PB–HAP emissions that do
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not exceed these new Tier 2 screening
levels are considered to pose no
unacceptable risks. If the PB–HAP
emissions for a facility exceed the Tier
2 screening emissions rate and data are
available, we may decide to conduct a
more refined Tier 3 multipathway
assessment. There are several analyses
that can be included in a Tier 3 screen
depending upon the extent of
refinement warranted, including
validating that the lake is fishable and
considering plume-rise to estimate
emissions lost above the mixing layer. If
the Tier 3 screen is exceeded, the EPA
may further refine the assessment.
In evaluating the potential
multipathway risk from emissions of
lead compounds, rather than developing
a screening emissions rate for them, we
compared maximum estimated chronic
inhalation exposures with the level of
the current National Ambient Air
Quality Standard (NAAQS) for lead.16
Values below the level of the primary
(health-based) lead NAAQS were
considered to have a low potential for
multipathway risk.
For further information on the
multipathway analysis approach, see
the Residual Risk Assessment for the
Aerospace Manufacturing and Rework
Facilities Source Category in Support of
the January, 2015 Risk and Technology
Review Proposal, January 2015, which is
available in the docket for this action.
5. How did we conduct the
environmental risk screening
assessment?
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a. Adverse Environmental Effect
The EPA conducts a screening
assessment to examine the potential for
adverse environmental effects as
required under section 112(f)(2)(A) of
the CAA. Section 112(a)(7) of the CAA
defines ‘‘adverse environmental effect’’
as ‘‘any significant and widespread
adverse effect, which may reasonably be
anticipated, to wildlife, aquatic life or
other natural resources, including
adverse impacts on populations of
endangered or threatened species or
significant degradation of
16 In doing so, EPA notes that the legal standard
for a primary NAAQS—that a standard is requisite
to protect public health and provide an adequate
margin of safety (CAA section 109(b))—differs from
the CAA section 112(f) standard (requiring among
other things that the standard provide an ‘‘ample
margin of safety’’). However, the lead NAAQS is a
reasonable measure of determining risk
acceptability (i.e., the first step of the Benzene
NESHAP analysis) since it is designed to protect the
most susceptible group in the human population—
children, including children living near major lead
emitting sources (73 FR 67002/3; 73 FR 67000/3; 73
FR 67005/1). In addition, applying the level of the
primary lead NAAQS at the risk acceptability step
is conservative, since that primary lead NAAQS
reflects an adequate margin of safety.
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environmental quality over broad
areas.’’
b. Environmental HAP
The EPA focuses on seven HAP,
which we refer to as ‘‘environmental
HAP,’’ in its screening analysis: Five
PB–HAP and two acid gases. The five
PB–HAP are cadmium, dioxins/furans,
POM, mercury (both inorganic mercury
and methyl mercury) and lead
compounds. The two acid gases are
hydrogen chloride (HCl) and hydrogen
fluoride (HF). The rationale for
including these seven HAP in the
environmental risk screening analysis is
presented below.
HAP that persist and bioaccumulate
are of particular environmental concern
because they accumulate in the soil,
sediment and water. The PB–HAP are
taken up, through sediment, soil, water
and/or ingestion of other organisms, by
plants or animals (e.g., small fish) at the
bottom of the food chain. As larger and
larger predators consume these
organisms, concentrations of the PB–
HAP in the animal tissues increases as
does the potential for adverse effects.
The five PB–HAP we evaluate as part of
our screening analysis account for 99.8
percent of all PB–HAP emissions
nationally from stationary sources (on a
mass basis from the 2005 NEI).
In addition to accounting for almost
all of the mass of PB–HAP emitted, we
note that the TRIM.FaTE model that we
use to evaluate multipathway risk
allows us to estimate concentrations of
cadmium compounds, dioxins/furans,
POM and mercury in soil, sediment and
water. For lead compounds, we
currently do not have the ability to
calculate these concentrations using the
TRIM.FaTE model. Therefore, to
evaluate the potential for adverse
environmental effects from lead
compounds, we compare the estimated
HEM-modeled exposures from the
source category emissions of lead with
the level of the secondary NAAQS for
lead.17 We consider values below the
level of the secondary NAAQS for lead
to be unlikely to cause adverse
environmental effects.
Due to their well-documented
potential to cause direct damage to
terrestrial plants, we include two acid
gases, HCl and HF, in the environmental
screening analysis. According to the
17 The secondary NAAQS for lead is a reasonable
measure of determining whether there is an adverse
environmental effect since it was established
considering ‘‘effects on soils, water, crops,
vegetation, man-made materials, animals, wildlife,
weather, visibility and climate, damage to and
deterioration of property, and hazards to
transportation, as well as effects on economic
values and on personal comfort and well-being.’’
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2005 NEI, HCl and HF account for about
99 percent (on a mass basis) of the total
acid gas HAP emitted by stationary
sources in the U.S. In addition to the
potential to cause direct damage to
plants, high concentrations of HF in the
air have been linked to fluorosis in
livestock. Air concentrations of these
HAP are already calculated as part of
the human multipathway exposure and
risk screening analysis using the HEM3–
AERMOD air dispersion model, and we
are able to use the air dispersion
modeling results to estimate the
potential for an adverse environmental
effect.
The EPA acknowledges that other
HAP beyond the seven HAP discussed
above may have the potential to cause
adverse environmental effects.
Therefore, the EPA may include other
relevant HAP in its environmental risk
screening in the future, as modeling
science and resources allow. The EPA
invites comment on the extent to which
other HAP emitted by the source
category may cause adverse
environmental effects. Such information
should include references to peerreviewed ecological effects benchmarks
that are of sufficient quality for making
regulatory decisions, as well as
information on the presence of
organisms located near facilities within
the source category that such
benchmarks indicate could be adversely
affected.
c. Ecological Assessment Endpoints and
Benchmarks for PB–HAP
An important consideration in the
development of the EPA’s screening
methodology is the selection of
ecological assessment endpoints and
benchmarks. Ecological assessment
endpoints are defined by the ecological
entity (e.g., aquatic communities
including fish and plankton) and its
attributes (e.g., frequency of mortality).
Ecological assessment endpoints can be
established for organisms, populations,
communities or assemblages and
ecosystems.
For PB–HAP (other than lead
compounds), we evaluated the
following community-level ecological
assessment endpoints to screen for
organisms directly exposed to HAP in
soils, sediment and water:
• Local terrestrial communities (i.e.,
soil invertebrates, plants) and
populations of small birds and
mammals that consume soil
invertebrates exposed to PB–HAP in the
surface soil.
• Local benthic (i.e., bottom sediment
dwelling insects, amphipods, isopods
and crayfish) communities exposed to
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PB–HAP in sediment in nearby water
bodies.
• Local aquatic (water-column)
communities (including fish and
plankton) exposed to PB–HAP in nearby
surface waters.
For PB–HAP (other than lead
compounds), we also evaluated the
population-level ecological assessment
endpoint to screen for indirect HAP
exposures of top consumers via the
bioaccumulation of HAP in food chains.
The endpoint evaluated was piscivorous
(i.e., fish-eating) wildlife consuming
PB–HAP-contaminated fish from nearby
water bodies.
For cadmium compounds, dioxins/
furans, POM and mercury, we identified
the available ecological benchmarks for
each assessment endpoint. An
ecological benchmark represents a
concentration of HAP (e.g., 0.77 mg of
HAP per liter of water) that has been
linked to a particular environmental
effect level (e.g., a no-observed-adverseeffect level (NOAEL)) through scientific
study. For PB–HAP, we identified,
where possible, ecological benchmarks
at the following effect levels:
• Probable effect levels (PEL): Level
above which adverse effects are
expected to occur frequently.
• Lowest-observed-adverse-effect
level (LOAEL): The lowest exposure
level tested at which there are
biologically significant increases in
frequency or severity of adverse effects.
• No-observed-adverse-effect levels
(NOAEL): The highest exposure level
tested at which there are no biologically
significant increases in the frequency or
severity of adverse effect.
We established a hierarchy of
preferred benchmark sources to allow
selection of benchmarks for each
environmental HAP at each ecological
assessment endpoint. In general, the
EPA sources that are used at a
programmatic level (e.g., Office of
Water, Superfund Program) were used,
if available. If not, the EPA benchmarks
used in regional programs (e.g.,
Superfund) were used. If benchmarks
were not available at a programmatic or
regional level, we used benchmarks
developed by other federal agencies
(e.g., National Oceanic and Atmospheric
Administration (NOAA)) or state
agencies.
Benchmarks for all effect levels are
not available for all PB–HAP and
assessment endpoints. In cases where
multiple effect levels were available for
a particular PB–HAP and assessment
endpoint, we use all of the available
effect levels to help us to determine
whether ecological risks exist and, if so,
whether the risks could be considered
significant and widespread.
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d. Ecological Assessment Endpoints and
Benchmarks for Acid Gases
The environmental screening analysis
also evaluated potential damage and
reduced productivity of plants due to
direct exposure to acid gases in the air.
For acid gases, we evaluated the
ecological assessment endpoint of local
terrestrial plant communities with
foliage exposed to acidic gaseous HAP
in the air.
The selection of ecological
benchmarks for the effects of acid gases
on plants followed the same approach
as for PB–HAP (i.e., we examine all of
the available chronic benchmarks). For
HCl, the EPA identified chronic
benchmark concentrations. We note that
the benchmark for chronic HCl exposure
to plants is greater than the reference
concentration for chronic inhalation
exposure for human health. This means
that where the EPA includes regulatory
requirements to prevent an exceedance
of the reference concentration for
human health, additional analyses for
adverse environmental effects of HCl
would not be necessary.
For HF, the EPA identified chronic
benchmark concentrations for plants
and evaluated chronic exposures to
plants in the screening analysis. High
concentrations of HF in the air have also
been linked to fluorosis in livestock.
However, the HF concentrations at
which fluorosis in livestock occur are
higher than those at which plant
damage begins. Therefore, the
benchmarks for plants are protective of
both plants and livestock.
e. Screening Methodology
For the environmental risk screening
analysis, the EPA first determined
whether any facilities in the Aerospace
Manufacturing and Rework Facilities
source category emitted any of the seven
environmental HAP. For the Aerospace
Manufacturing and Rework Facilities
source category, we identified emissions
of five PB–HAP and two acid gases as
the environmental HAP. The five PB–
HAP are cadmium, dioxins/furans,
POM, mercury (both inorganic mercury
and methyl mercury) and lead
compounds. The two acid gases are HCl
and HF.
Because one or more of the seven
environmental HAP evaluated are
emitted by at least one facility in the
source category, we proceeded to the
second step of the evaluation.
f. PB–HAP Methodology
For cadmium, mercury, POM and
dioxins/furans, the environmental
screening analysis consists of two tiers,
while lead compounds are analyzed
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differently as discussed earlier. In the
first tier, we determined whether the
maximum facility-specific emission
rates of each of the emitted
environmental HAP were large enough
to create the potential for adverse
environmental effects under reasonable
worst-case environmental conditions.
These are the same environmental
conditions used in the human
multipathway exposure and risk
screening analysis.
To facilitate this step, TRIM.FaTE was
run for each PB–HAP under
hypothetical environmental conditions
designed to provide conservatively high
HAP concentrations. The model was set
to maximize runoff from terrestrial
parcels into the modeled lake, which in
turn, maximized the chemical
concentrations in the water, the
sediments and the fish. The resulting
media concentrations were then used to
back-calculate a screening level
emission rate that corresponded to the
relevant exposure benchmark
concentration value for each assessment
endpoint. To assess emissions from a
facility, the reported emission rate for
each PB–HAP was compared to the
screening level emission rate for that
PB–HAP for each assessment endpoint.
If emissions from a facility do not
exceed the Tier 1 screening level, the
facility ‘‘passes’’ the screen, and,
therefore, is not evaluated further under
the screening approach. If emissions
from a facility exceed the Tier 1
screening level, we evaluate the facility
further in Tier 2.
In Tier 2 of the environmental
screening analysis, the emission rate
screening levels are adjusted to account
for local meteorology and the actual
location of lakes in the vicinity of
facilities that did not pass the Tier 1
screen. The modeling domain for each
facility in the Tier 2 analysis consists of
eight octants. Each octant contains five
modeled soil concentrations at various
distances from the facility (5 soil
concentrations × 8 octants = total of 40
soil concentrations per facility) and one
lake with modeled concentrations for
water, sediment and fish tissue. In the
Tier 2 environmental risk screening
analysis, the 40 soil concentration
points are averaged to obtain an average
soil concentration for each facility for
each PB–HAP. For the water, sediment
and fish tissue concentrations, the
highest value for each facility for each
pollutant is used. If emission
concentrations from a facility do not
exceed the Tier 2 screening level, the
facility passes the screen, and typically
is not evaluated further. If emissions
from a facility exceed the Tier 2
screening level, the facility does not
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pass the screen and, therefore, may have
the potential to cause adverse
environmental effects. Such facilities
are evaluated further to investigate
factors such as the magnitude and
characteristics of the area of exceedance.
tkelley on DSK3SPTVN1PROD with PROPOSALS2
g. Acid Gas Methodology
The environmental screening analysis
evaluates the potential phytotoxicity
and reduced productivity of plants due
to chronic exposure to acid gases. The
environmental risk screening
methodology for acid gases is a singletier screen that compares the average
off-site ambient air concentration over
the modeling domain to ecological
benchmarks for each of the acid gases.
Because air concentrations are
compared directly to the ecological
benchmarks, emission-based screening
levels are not calculated for acid gases
as they are in the ecological risk
screening methodology for PB–HAP.
For purposes of ecological risk
screening, the EPA identifies a potential
for adverse environmental effects to
plant communities from exposure to
acid gases when the average
concentration of the HAP around a
facility exceeds the LOAEL ecological
benchmark. In such cases, we further
investigate factors such as the
magnitude and characteristics of the
area of exceedance (e.g., land use of
exceedance area, size of exceedance
area) to determine if there is an adverse
environmental effect.
For further information on the
environmental screening analysis
approach, see the Residual Risk
Assessment for the Aerospace
Manufacturing and Rework Facilities
Source Category in Support of the
January, 2015 Risk and Technology
Review Proposal, January 2015, which is
available in the docket for this action.
6. How did we conduct facility-wide
assessments?
To put the source category risks in
context, we typically examine the risks
from the entire ‘‘facility,’’ where the
facility includes all HAP-emitting
operations within a contiguous area and
under common control. In other words,
we examine the HAP emissions not only
from the source category emission
points of interest, but also emissions of
HAP from all other emission sources at
the facility for which we have data.
The emissions inventories developed
from the 2011 and 2012 ICRs, 2011 NEI
and 2005 NATA include emissions
information for all emissions sources at
the facilities that are part of the
Aerospace Manufacturing and Rework
Facilities source category. These include
sources currently regulated by the
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Aerospace NESHAP: Primer/topcoat
application operations, waste handling
operations, chemical milling maskant
application operations, cleaning
operations and chemical and blast
depainting operations. These also
include emission sources not currently
regulated by the Aerospace NESHAP:
Specialty coatings, composite
processing, chemical milling and metal
finishing, wastewater, storage tanks,
boilers, engines, chemical
manufacturing processes, secondary
metal production processes, heaters, soil
remediation, transportation equipment,
waste disposal, welding and other
miscellaneous manufacturing processes.
We analyzed risks due to the
inhalation of HAP that are emitted
‘‘facility-wide’’ for the populations
residing within 50 km of each facility,
consistent with the methods used for
the source category analysis described
above. For these facility-wide risk
analyses, the modeled source category
risks were compared to the facility-wide
risks to determine the portion of facilitywide risks that could be attributed to the
source category addressed in this
proposal. We specifically examined the
facility that was associated with the
highest estimate of risk and determined
the percentage of that risk attributable to
the source category of interest. The
Residual Risk Assessment for the
Aerospace Manufacturing and Rework
Facilities Source Category in Support of
the January, 2015 Risk and Technology
Review Proposal, January 2015,
available through the docket for this
action, provides the methodology and
results of the facility-wide analyses,
including all facility-wide risks and the
percentage of source category
contribution to facility-wide risks.
7. How did we consider uncertainties in
risk assessment?
In the Benzene NESHAP, we
concluded that risk estimation
uncertainty should be considered in our
decision-making under the ample
margin of safety framework. Uncertainty
and the potential for bias are inherent in
all risk assessments, including those
performed for this proposal. Although
uncertainty exists, we believe that our
approach, which used conservative
tools and assumptions, ensures that our
decisions are health protective and
environmentally protective. A brief
discussion of the uncertainties in the
RTR emissions dataset, dispersion
modeling, inhalation exposure estimates
and dose-response relationships follows
below. A more thorough discussion of
these uncertainties is included in the
Residual Risk Assessment for the
Aerospace Manufacturing and Rework
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Facilities Source Category in Support of
the January, 2015 Risk and Technology
Review Proposal, January 2015, which is
available in the docket for this action.
a. Uncertainties in the RTR Emissions
Dataset
Although the development of the RTR
emissions dataset involved quality
assurance/quality control processes, the
accuracy of emissions values will vary
depending on the source of the data, the
degree to which data are incomplete or
missing, the degree to which
assumptions made to complete the
datasets are accurate, and errors in
emission estimates and other factors.
The emission estimates considered in
this analysis are annual totals for certain
years, and they do not reflect short-term
fluctuations during the course of a year
or variations from year to year. The
estimates of peak hourly emission rates
for the acute effects screening
assessment were based on an emission
adjustment factor applied to the average
annual hourly emission rates, which are
intended to account for emission
fluctuations due to normal facility
operations.
b. Uncertainties in Dispersion Modeling
We recognize there is uncertainty in
ambient concentration estimates
associated with any model, including
the EPA’s recommended regulatory
dispersion model, AERMOD. In using a
model to estimate ambient pollutant
concentrations, the user chooses certain
options to apply. For RTR assessments,
we select some model options that have
the potential to overestimate ambient air
concentrations (e.g., not including
plume depletion or pollutant
transformation). We select other model
options that have the potential to
underestimate ambient impacts (e.g., not
including building downwash). Other
options that we select have the potential
to either under- or overestimate ambient
levels (e.g., meteorology and receptor
locations). On balance, considering the
directional nature of the uncertainties
commonly present in ambient
concentrations estimated by dispersion
models, the approach we apply in the
RTR assessments should yield unbiased
estimates of ambient HAP
concentrations.
c. Uncertainties in Inhalation Exposure
The EPA did not include the effects
of human mobility on exposures in the
assessment. Specifically, short-term
mobility and long-term mobility
between census blocks in the modeling
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domain were not considered.18 The
approach of not considering short or
long-term population mobility does not
bias the estimate of the theoretical MIR
(by definition), nor does it affect the
estimate of cancer incidence because the
total population number remains the
same. It does, however, affect the shape
of the distribution of individual risks
across the affected population, shifting
it toward higher estimated individual
risks at the upper end and reducing the
number of people estimated to be at
lower risks, thereby increasing the
estimated number of people at specific
high risk levels (e.g., 1-in-10 thousand
or 1-in-1 million).
In addition, the assessment predicted
the chronic exposures at the centroid of
each populated census block as
surrogates for the exposure
concentrations for all people living in
that block. Using the census block
centroid to predict chronic exposures
tends to over-predict exposures for
people in the census block who live
farther from the facility and underpredict exposures for people in the
census block who live closer to the
facility. Thus, using the census block
centroid to predict chronic exposures
may lead to a potential understatement
or overstatement of the true maximum
impact, but is an unbiased estimate of
average risk and incidence. We reduce
this uncertainty by analyzing large
census blocks near facilities using aerial
imagery and adjusting the location of
the block centroid to better represent the
population in the block, as well as
adding additional receptor locations
where the block population is not well
represented by a single location.
The assessment evaluates the cancer
inhalation risks associated with
pollutant exposures over a 70-year
period, which is the assumed lifetime of
an individual. In reality, both the length
of time that modeled emission sources
at facilities actually operate (i.e., more
or less than 70 years) and the domestic
growth or decline of the modeled
industry (i.e., the increase or decrease in
the number or size of domestic
facilities) will influence the future risks
posed by a given source or source
category. Depending on the
characteristics of the industry, these
factors will, in most cases, result in an
overestimate both in individual risk
levels and in the total estimated number
of cancer cases. However, in the
unlikely scenario where a facility
maintains, or even increases, its
18 Short-term mobility is movement from one
micro-environment to another over the course of
hours or days. Long-term mobility is movement
from one residence to another over the course of a
lifetime.
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emissions levels over a period of more
than 70 years, residents live beyond 70
years at the same location, and the
residents spend most of their days at
that location, then the cancer inhalation
risks could potentially be
underestimated. However, annual
cancer incidence estimates from
exposures to emissions from these
sources would not be affected by the
length of time an emissions source
operates.
The exposure estimates used in these
analyses assume chronic exposures to
ambient (outdoor) levels of pollutants.
Because most people spend the majority
of their time indoors, actual exposures
may not be as high, depending on the
characteristics of the pollutants
modeled. For many of the HAP, indoor
levels are roughly equivalent to ambient
levels, but for very reactive pollutants or
larger particles, indoor levels are
typically lower. This factor has the
potential to result in an overestimate of
25 to 30 percent of exposures.19
In addition to the uncertainties
highlighted above, there are several
factors specific to the acute exposure
assessment that the EPA conducts as
part of the risk review under section 112
of the CAA that should be highlighted.
The accuracy of an acute inhalation
exposure assessment depends on the
simultaneous occurrence of
independent factors that may vary
greatly, such as hourly emissions rates,
meteorology and the presence of
humans at the location of the maximum
concentration. In the acute screening
assessment that we conduct under the
RTR program, we assume that peak
emissions from the source category and
worst-case meteorological conditions
co-occur, thus, resulting in maximum
ambient concentrations. These two
events are unlikely to occur at the same
time, making these assumptions
conservative. We then include the
additional assumption that a person is
located at this point during this same
time period. For this source category,
these assumptions would tend to be
worst-case actual exposures as it is
unlikely that a person would be located
at the point of maximum exposure
during the time when peak emissions
and worst-case meteorological
conditions occur simultaneously.
d. Uncertainties in Dose-Response
Relationships
There are uncertainties inherent in
the development of the dose-response
values used in our risk assessments for
19 U.S. EPA. National-Scale Air Toxics
Assessment for 1996. EPA 453/R–01–003; January
2001; page 85.
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cancer effects from chronic exposures
and non-cancer effects from both
chronic and acute exposures. Some
uncertainties may be considered
quantitatively, and others generally are
expressed in qualitative terms. We note
as a preface to this discussion a point on
dose-response uncertainty that is
brought out in the EPA’s 2005 Cancer
Guidelines; namely, that ‘‘the primary
goal of EPA actions is protection of
human health; accordingly, as an
Agency policy, risk assessment
procedures, including default options
that are used in the absence of scientific
data to the contrary, should be health
protective’’ (EPA 2005 Cancer
Guidelines, pages 1–7). This is the
approach followed here as summarized
in the next several paragraphs. A
complete detailed discussion of
uncertainties and variability in doseresponse relationships is given in the
Residual Risk Assessment for the
Aerospace Manufacturing and Rework
Facilities Source Category in Support of
the January, 2015 Risk and Technology
Review Proposal, January 2015, which is
available in the docket for this action.
Cancer URE values used in our risk
assessments are those that have been
developed to generally provide an upper
bound estimate of risk. That is, they
represent a ‘‘plausible upper limit to the
true value of a quantity’’ (although this
is usually not a true statistical
confidence limit).20 In some
circumstances, the true risk could be as
low as zero; however, in other
circumstances the risk could be
greater.21 When developing an upper
bound estimate of risk and to provide
risk values that do not underestimate
risk, health-protective default
approaches are generally used. To err on
the side of ensuring adequate health
protection, the EPA typically uses the
upper bound estimates rather than
lower bound or central tendency
estimates in our risk assessments, an
approach that may have limitations for
other uses (e.g., priority-setting or
expected benefits analysis).
Chronic non-cancer RfC and reference
dose (RfD) values represent chronic
exposure levels that are intended to be
health-protective levels. Specifically,
these values provide an estimate (with
uncertainty spanning perhaps an order
of magnitude) of a continuous
inhalation exposure (RfC) or a daily oral
exposure (RfD) to the human population
20 IRIS glossary (https://www.epa.gov/NCEA/iris/
help_gloss.htm).
21 An exception to this is the URE for benzene,
which is considered to cover a range of values, each
end of which is considered to be equally plausible,
and which is based on maximum likelihood
estimates.
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(including sensitive subgroups) that is
likely to be without an appreciable risk
of deleterious effects during a lifetime.
To derive values that are intended to be
‘‘without appreciable risk,’’ the
methodology relies upon an uncertainty
factor (UF) approach (U.S. EPA, 1993,
1994) 22 23 which considers uncertainty,
variability and gaps in the available
data. The UF are applied to derive
reference values that are intended to
protect against appreciable risk of
deleterious effects. The UF are
commonly default values 24 (e.g., factors
of 10 or 3) used in the absence of
compound-specific data; where data are
available, UF may also be developed
using compound-specific information.
When data are limited, more
assumptions are needed and more UF
are used. Thus, there may be a greater
tendency to overestimate risk in the
sense that further study might support
development of reference values that are
higher (i.e., less potent) because fewer
default assumptions are needed.
However, for some pollutants, it is
possible that risks may be
underestimated.
While collectively termed ‘‘UF,’’ these
factors account for a number of different
quantitative considerations when using
observed animal (usually rodent) or
human toxicity data in the development
of the RfC. The UF are intended to
account for: (1) Variation in
susceptibility among the members of the
human population (i.e., inter-individual
variability); (2) uncertainty in
extrapolating from experimental animal
data to humans (i.e., interspecies
differences); (3) uncertainty in
extrapolating from data obtained in a
22 U.S. EPA. Reference Dose (RfD): Description
and Use in Health Risk Assessments. Dated March
1993.
23 U.S. EPA. Methods for Derivation of Inhalation
Reference Concentrations and Application of
Inhalation Dosimetry. EPA/600/8–90/066F. Dated
October 1994.
24 According to the NRC report, Science and
Judgment in Risk Assessment (NRC, 1994)
‘‘[Default] options are generic approaches, based on
general scientific knowledge and policy judgment,
that are applied to various elements of the risk
assessment process when the correct scientific
model is unknown or uncertain.’’ The 1983 NRC
report, Risk Assessment in the Federal Government:
Managing the Process, defined default option as
‘‘the option chosen on the basis of risk assessment
policy that appears to be the best choice in the
absence of data to the contrary’’ (NRC, 1983a, p. 63).
Therefore, default options are not rules that bind
the agency; rather, the agency may depart from
them in evaluating the risks posed by a specific
substance when it believes this to be appropriate.
In keeping with EPA’s goal of protecting public
health and the environment, default assumptions
are used to ensure that risk to chemicals is not
underestimated (although defaults are not intended
to overtly overestimate risk). See EPA, 2004, An
Examination of EPA Risk Assessment Principles
and Practices, EPA/100/B–04/001 available at:
https://www.epa.gov/osa/pdfs/ratf-final.pdf.
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study with less-than-lifetime exposure
(i.e., extrapolating from sub-chronic to
chronic exposure); (4) uncertainty in
extrapolating the observed data to
obtain an estimate of the exposure
associated with no adverse effects; and
(5) uncertainty when the database is
incomplete or there are problems with
the applicability of available studies.
Many of the UF used to account for
variability and uncertainty in the
development of acute reference values
are quite similar to those developed for
chronic durations, but they more often
use individual UF values that may be
less than 10. The UF are applied based
on chemical-specific or health effectspecific information (e.g., simple
irritation effects do not vary appreciably
between human individuals, hence a
value of 3 is typically used), or based on
the purpose for the reference value (see
the following paragraph). The UF
applied in acute reference value
derivation include: (1) Heterogeneity
among humans; (2) uncertainty in
extrapolating from animals to humans;
(3) uncertainty in lowest observed
adverse effect (exposure) level to no
observed adverse effect (exposure) level
adjustments; and (4) uncertainty in
accounting for an incomplete database
on toxic effects of potential concern.
Additional adjustments are often
applied to account for uncertainty in
extrapolation from observations at one
exposure duration (e.g., 4 hours) to
derive an acute reference value at
another exposure duration (e.g., 1 hour).
Not all acute reference values are
developed for the same purpose and
care must be taken when interpreting
the results of an acute assessment of
human health effects relative to the
reference value or values being
exceeded. Where relevant to the
estimated exposures, the lack of shortterm dose-response values at different
levels of severity should be factored into
the risk characterization as potential
uncertainties.
For a group of compounds that are
unspeciated (e.g., glycol ethers), we
conservatively use the most protective
reference value of an individual
compound in that group to estimate
risk. Similarly, for an individual
compound in a group (e.g., ethylene
glycol diethyl ether) that does not have
a specified reference value, we also
apply the most protective reference
value from the other compounds in the
group to estimate risk.
e. Uncertainties in the Multipathway
Assessment
For each source category, we
generally rely on site-specific levels of
PB–HAP emissions to determine
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whether a refined assessment of the
impacts from multipathway exposures
is necessary. This determination is
based on the results of a three-tiered
screening analysis that relies on the
outputs from models that estimate
environmental pollutant concentrations
and human exposures for four PB–HAP.
Two important types of uncertainty
associated with the use of these models
in RTR risk assessments and inherent to
any assessment that relies on
environmental modeling are model
uncertainty and input uncertainty.25
Model uncertainty concerns whether
the selected models are appropriate for
the assessment being conducted and
whether they adequately represent the
actual processes that might occur for
that situation. An example of model
uncertainty is the question of whether
the model adequately describes the
movement of a pollutant through the
soil. This type of uncertainty is difficult
to quantify. However, based on feedback
received from previous EPA SAB
reviews and other reviews, we are
confident that the models used in the
screen are appropriate and state-of-theart for the multipathway risk
assessments conducted in support of
RTR.
Input uncertainty is concerned with
how accurately the models have been
configured and parameterized (i.e.,
represented in terms of measurable or
estimable variables) for the assessment
at hand. For Tier 1 of the multipathway
screen, we configured the models to
avoid underestimating exposure and
risk. This was accomplished by
selecting upper-end values from
nationally representative datasets for the
more influential parameters in the
environmental model, including
selection and spatial configuration of
the area of interest, lake location and
size, meteorology, surface water and soil
characteristics and structure of the
aquatic food web. We also assume an
ingestion exposure scenario and values
for human exposure factors that
represent reasonable maximum
exposures.
In Tier 2 of the multipathway
assessment, we refine the model inputs
to account for meteorological patterns in
the vicinity of the facility versus using
upper-end national values and we
identify the actual location of lakes near
the facility rather than the default lake
location that we apply in Tier 1. By
25 In the context of this discussion, the term
‘‘uncertainty’’ as it pertains to exposure and risk
encompasses both variability in the range of
expected inputs and screening results due to
existing spatial, temporal and other factors, as well
as uncertainty in being able to accurately estimate
the true result.
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refining the screening approach in Tier
2 to account for local geographical and
meteorological data, we decrease the
likelihood that concentrations in
environmental media are overestimated,
thereby increasing the usefulness of the
screen. The assumptions and the
associated uncertainties regarding the
selected ingestion exposure scenario are
the same for Tier 1 and Tier 2.
For both Tiers 1 and 2 of the
multipathway assessment, our approach
to addressing model input uncertainty is
generally cautious. We choose model
inputs from the upper end of the range
of possible values for the influential
parameters used in the models, and we
assume that the exposed individual
exhibits ingestion behavior that would
lead to a high total exposure. This
approach reduces the likelihood of not
identifying high risks for adverse
impacts.
Despite the uncertainties, when
individual pollutants or facilities do
screen out, we are confident that the
potential for adverse multipathway
impacts on human health is very low.
On the other hand, when individual
pollutants or facilities do not screen out,
it does not mean that multipathway
impacts are significant, only that we
cannot rule out that possibility and that
a refined multipathway analysis for the
site might be necessary to obtain a more
accurate risk characterization for the
source category.
For further information on
uncertainties and the Tier 1 and 2
screening methods, refer to Appendix 4
of Modeling File Preparation Memo.
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f. Uncertainties in the Environmental
Risk Screening Assessment
For each source category, we
generally rely on site-specific levels of
environmental HAP emissions to
perform an environmental screening
assessment. The environmental
screening assessment is based on the
outputs from models that estimate
environmental HAP concentrations. The
same models, specifically the
TRIM.FaTE multipathway model and
the AERMOD air dispersion model, are
used to estimate environmental HAP
concentrations for both the human
multipathway screening analysis and for
the environmental screening analysis.
Therefore, both screening assessments
have similar modeling uncertainties.
Two important types of uncertainty
associated with the use of these models
in RTR environmental screening
assessments—and inherent to any
assessment that relies on environmental
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modeling—are model uncertainty and
input uncertainty.26
Model uncertainty concerns whether
the selected models are appropriate for
the assessment being conducted and
whether they adequately represent the
movement and accumulation of
environmental HAP emissions in the
environment. For example, does the
model adequately describe the
movement of a pollutant through the
soil? This type of uncertainty is difficult
to quantify. However, based on feedback
received from previous EPA SAB
reviews and other reviews, we are
confident that the models used in the
screen are appropriate and state-of-theart for the environmental risk
assessments conducted in support of
our RTR analyses.
Input uncertainty is concerned with
how accurately the models have been
configured and parameterized for the
assessment at hand. For Tier 1 of the
environmental screen for PB–HAP, we
configured the models to avoid
underestimating exposure and risk to
reduce the likelihood that the results
indicate the risks are lower than they
actually are. This was accomplished by
selecting upper-end values from
nationally-representative datasets for
the more influential parameters in the
environmental model, including
selection and spatial configuration of
the area of interest, the location and size
of any bodies of water, meteorology,
surface water and soil characteristics
and structure of the aquatic food web.
In Tier 1, we used the maximum
facility-specific emissions for the PB–
HAP (other than lead compounds,
which were evaluated by comparison to
the secondary lead NAAQS) that were
included in the environmental
screening assessment and each of the
media when comparing to ecological
benchmarks. This is consistent with the
conservative design of Tier 1 of the
screen. In Tier 2 of the environmental
screening analysis for PB–HAP, we
refine the model inputs to account for
meteorological patterns in the vicinity
of the facility versus using upper-end
national values, and we identify the
locations of water bodies near the
facility location. By refining the
screening approach in Tier 2 to account
for local geographical and
meteorological data, we decrease the
likelihood that concentrations in
environmental media are overestimated,
26 In the context of this discussion, the term
‘‘uncertainty,’’ as it pertains to exposure and risk
assessment, encompasses both variability in the
range of expected inputs and screening results due
to existing spatial, temporal and other factors, as
well as uncertainty in being able to accurately
estimate the true result.
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8409
thereby increasing the usefulness of the
screen. To better represent widespread
impacts, the modeled soil
concentrations are averaged in Tier 2 to
obtain one average soil concentration
value for each facility and for each PB–
HAP. For PB–HAP concentrations in
water, sediment and fish tissue, the
highest value for each facility for each
pollutant is used.
For the environmental screening
assessment for acid gases, we employ a
single-tiered approach. We use the
modeled air concentrations and
compare those with ecological
benchmarks.
For both Tiers 1 and 2 of the
environmental screening assessment,
our approach to addressing model input
uncertainty is generally cautious. We
choose model inputs from the upper
end of the range of possible values for
the influential parameters used in the
models, and we assume that the
exposed individual exhibits ingestion
behavior that would lead to a high total
exposure. This approach reduces the
likelihood of not identifying potential
risks for adverse environmental impacts.
Uncertainty also exists in the
ecological benchmarks for the
environmental risk screening analysis.
We established a hierarchy of preferred
benchmark sources to allow selection of
benchmarks for each environmental
HAP at each ecological assessment
endpoint. In general, EPA benchmarks
for programmatic levels (e.g., Office of
Water, Superfund Program) were used if
available. If not, we used EPA
benchmarks used in regional programs
(e.g., Superfund Program). If
benchmarks were not available at a
programmatic or regional level, we used
benchmarks developed by other
agencies (e.g., NOAA) or by state
agencies.
In all cases (except for lead
compounds, which were evaluated
through a comparison to the NAAQS),
we searched for benchmarks at the
following three effect levels, as
described in section III.A.5 of this
preamble:
1. A no-effect level (i.e., NOAEL).
2. Threshold-effect level (i.e.,
LOAEL).
3. Probable effect level (i.e., PEL).
For some ecological assessment
endpoint/environmental HAP
combinations, we could identify
benchmarks for all three effect levels,
but for most, we could not. In one case,
where different agencies derived
significantly different numbers to
represent a threshold for effect, we
included both. In several cases, only a
single benchmark was available. In
cases where multiple effect levels were
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available for a particular PB–HAP and
assessment endpoint, we used all of the
available effect levels to help us to
determine whether risk exists and if the
risks could be considered significant
and widespread.
The EPA evaluates the following
seven HAP in the environmental risk
screening assessment: Cadmium,
dioxins/furans, POM, mercury (both
inorganic mercury and methyl mercury),
lead compounds, HCl and HF, where
applicable. These seven HAP represent
pollutants that can cause adverse
impacts for plants and animals either
through direct exposure to HAP in the
air or through exposure to HAP that is
deposited from the air onto soils and
surface waters. These seven HAP also
represent those HAP for which we can
conduct a meaningful environmental
risk screening assessment. For other
HAP not included in our screening
assessment, the model has not been
parameterized such that it can be used
for that purpose. In some cases,
depending on the HAP, we may not
have appropriate multipathway models
that allow us to predict the
concentration of that pollutant. The EPA
acknowledges that other HAP beyond
the seven HAP that we are evaluating
may have the potential to cause adverse
environmental effects and, therefore, the
EPA may evaluate other relevant HAP in
the future, as modeling science and
resources allow.
Further information on uncertainties
and the Tier 1 and 2 environmental
screening methods is provided in
Appendix 5 of the document, Technical
Support Document for TRIM-Based
Multipathway Tiered Screening
Methodology for RTR: Summary of
Approach and Evaluation. Also, see the
Residual Risk Assessment for the
Aerospace Manufacturing and Rework
Facilities Source Category in Support of
the January, 2015 Risk and Technology
Review Proposal, January 2015,
available in the docket for this action.
B. How did we consider the risk results
in making decisions for this proposal?
As discussed in section II.A of this
preamble, in evaluating and developing
standards under CAA section 112(f)(2),
we apply a two-step process to address
residual risk. In the first step, the EPA
determines whether risks are acceptable.
This determination ‘‘considers all health
information, including risk estimation
uncertainty, and includes a presumptive
limit on maximum individual lifetime
[cancer] risk (MIR) 27 of approximately
27 Although defined as ‘‘maximum individual
risk,’’ MIR refers only to cancer risk. MIR, one
metric for assessing cancer risk, is the estimated
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[1-in-10 thousand] [i.e., 100-in-1
million].’’ 54 FR 38045, September 14,
1989. If risks are unacceptable, the EPA
must determine the emissions standards
necessary to bring risks to an acceptable
level without considering costs. In the
second step of the process, the EPA
considers whether the emissions
standards provide an ample margin of
safety ‘‘in consideration of all health
information, including the number of
persons at risk levels higher than
approximately 1-in-1 million, as well as
other relevant factors, including costs
and economic impacts, technological
feasibility, and other factors relevant to
each particular decision.’’ Id. The EPA
must promulgate emission standards
necessary to provide an ample margin of
safety.
In past residual risk actions, the EPA
considered a number of human health
risk metrics associated with emissions
from the categories under review,
including the MIR, the number of
persons in various risk ranges, cancer
incidence, the maximum non-cancer HI
and the maximum acute non-cancer
hazard. See, e.g., 72 FR 25138, May 3,
2007; 71 FR 42724, July 27, 2006. The
EPA considered this health information
for both actual and allowable emissions.
See, e.g., 75 FR 65068, October 21, 2010;
75 FR 80220, December 21, 2010; 76 FR
29032, May 19, 2011. The EPA also
discussed risk estimation uncertainties
and considered the uncertainties in the
determination of acceptable risk and
ample margin of safety in these past
actions. The EPA considered this same
type of information in support of this
action.
The agency is considering these
various measures of health information
to inform our determinations of risk
acceptability and ample margin of safety
under CAA section 112(f). As explained
in the Benzene NESHAP, ‘‘the first step
judgment on acceptability cannot be
reduced to any single factor’’ and, thus,
‘‘[t]he Administrator believes that the
acceptability of risk under [previous]
section 112 is best judged on the basis
of a broad set of health risk measures
and information.’’ 54 FR 38046,
September 14, 1989. Similarly, with
regard to the ample margin of safety
determination, ‘‘the Agency again
considers all of the health risk and other
health information considered in the
first step. Beyond that information,
additional factors relating to the
appropriate level of control will also be
considered, including cost and
economic impacts of controls,
risk were an individual exposed to the maximum
level of a pollutant for a lifetime.
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technological feasibility, uncertainties,
and any other relevant factors.’’ Id.
The Benzene NESHAP approach
provides flexibility regarding factors the
EPA may consider in making
determinations and how the EPA may
weigh those factors for each source
category. In responding to comment on
our policy under the Benzene NESHAP,
the EPA explained that:
[t]he policy chosen by the Administrator
permits consideration of multiple measures
of health risk. Not only can the MIR figure
be considered, but also incidence, the
presence of non-cancer health effects, and the
uncertainties of the risk estimates. In this
way, the effect on the most exposed
individuals can be reviewed as well as the
impact on the general public. These factors
can then be weighed in each individual case.
This approach complies with the Vinyl
Chloride mandate that the Administrator
ascertain an acceptable level of risk to the
public by employing [her] expertise to assess
available data. It also complies with the
Congressional intent behind the CAA, which
did not exclude the use of any particular
measure of public health risk from the EPA’s
consideration with respect to CAA section
112 regulations, and thereby implicitly
permits consideration of any and all
measures of health risk which the
Administrator, in [her] judgment, believes are
appropriate to determining what will ‘protect
the public health’.
See 54 FR at 38057, September 14, 1989.
Thus, the level of the MIR is only one
factor to be weighed in determining
acceptability of risks. The Benzene
NESHAP explained that ‘‘an MIR of
approximately 1-in-10 thousand should
ordinarily be the upper end of the range
of acceptability. As risks increase above
this benchmark, they become
presumptively less acceptable under
CAA section 112, and would be
weighed with the other health risk
measures and information in making an
overall judgment on acceptability. Or,
the Agency may find, in a particular
case, that a risk that includes MIR less
than the presumptively acceptable level
is unacceptable in the light of other
health risk factors.’’ Id. at 38045.
Similarly, with regard to the ample
margin of safety analysis, the EPA stated
in the Benzene NESHAP that: ‘‘EPA
believes the relative weight of the many
factors that can be considered in
selecting an ample margin of safety can
only be determined for each specific
source category. This occurs mainly
because technological and economic
factors (along with the health-related
factors) vary from source category to
source category.’’ Id. at 38061. We also
consider the uncertainties associated
with the various risk analyses, as
discussed earlier in this preamble, in
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our determinations of acceptability and
ample margin of safety.
The EPA notes that it has not
considered certain health information to
date in making residual risk
determinations. At this time, we do not
attempt to quantify those HAP risks that
may be associated with emissions from
other facilities that do not include the
source categories in question, mobile
source emissions, natural source
emissions, persistent environmental
pollution or atmospheric transformation
in the vicinity of the sources in these
categories.
The agency understands the potential
importance of considering an
individual’s total exposure to HAP in
addition to considering exposure to
HAP emissions from the source category
and facility. We recognize that such
consideration may be particularly
important when assessing non-cancer
risks, where pollutant-specific exposure
health reference levels (e.g., RfCs) are
based on the assumption that thresholds
exist for adverse health effects. For
example, the agency recognizes that,
although exposures attributable to
emissions from a source category or
facility alone may not indicate the
potential for increased risk of adverse
non-cancer health effects in a
population, the exposures resulting
from emissions from the facility in
combination with emissions from all of
the other sources (e.g., other facilities) to
which an individual is exposed may be
sufficient to result in increased risk of
adverse non-cancer health effects. In
May 2010, the SAB advised the EPA
‘‘that RTR assessments will be most
useful to decision makers and
communities if results are presented in
the broader context of aggregate and
cumulative risks, including background
concentrations and contributions from
other sources in the area.’’ 28
In response to the SAB
recommendations, the EPA is
incorporating cumulative risk analyses
into its RTR risk assessments, including
those reflected in this proposal. The
agency is: (1) Conducting facility-wide
assessments, which include source
category emission points as well as
other emission points within the
facilities; (2) considering sources in the
same category whose emissions result in
exposures to the same individuals; and
28 EPA’s responses to this and all other key
recommendations of the SAB’s advisory on RTR
risk assessment methodologies (which is available
at: https://yosemite.epa.gov/sab/sabproduct.nsf/
4AB3966E263D943A8525771F00668381/$File/EPASAB-10-007-unsigned.pdf) are outlined in a memo
to this rulemaking docket from David Guinnup
entitled, EPA’s Actions in Response to the Key
Recommendations of the SAB Review of RTR Risk
Assessment Methodologies.
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(3) for some persistent and
bioaccumulative pollutants, analyzing
the ingestion route of exposure. In
addition, the RTR risk assessments have
always considered aggregate cancer risk
from all carcinogens and aggregate noncancer hazard indices from all noncarcinogens affecting the same target
organ system.
Although we are interested in placing
source category and facility-wide HAP
risks in the context of total HAP risks
from all sources combined in the
vicinity of each source, we are
concerned about the uncertainties of
doing so. Because of the contribution to
total HAP risk from emission sources
other than those that we have studied in
depth during this RTR review, such
estimates of total HAP risks would have
significantly greater associated
uncertainties than the source category or
facility-wide estimates. Such aggregate
or cumulative assessments would
compound those uncertainties, making
the assessments too unreliable.
C. How did we perform the technology
review?
Our technology review focused on the
identification and evaluation of
developments in practices, processes
and control technologies that have
occurred since the MACT standards
were promulgated. Where we identified
such developments, in order to inform
our decision of whether it is
‘‘necessary’’ to revise the emissions
standards, we analyzed the technical
feasibility of applying these
developments and the estimated costs,
energy implications, non-air
environmental impacts, as well as
considering the emission reductions.
We also considered the appropriateness
of applying controls to new sources
versus retrofitting existing sources.
Based on our analyses of the available
data and information, we identified
potential developments in practices,
processes and control technologies. For
this exercise, we considered any of the
following to be a ‘‘development’’:
• Any add-on control technology or
other equipment that was not identified
and considered during development of
the original MACT standards.
• Any improvements in add-on
control technology or other equipment
(that were identified and considered
during development of the original
MACT standards) that could result in
additional emissions reduction.
• Any work practice or operational
procedure that was not identified or
considered during development of the
original MACT standards.
• Any process change or pollution
prevention alternative that could be
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broadly applied to the industry and that
was not identified or considered during
development of the original MACT
standards.
• Any significant changes in the cost
(including cost effectiveness) of
applying controls (including controls
the EPA considered during the
development of the original MACT
standards).
We reviewed a variety of data sources
in our investigation of potential
practices, processes or controls to
consider. Among the sources we
reviewed were the NESHAP for various
industries that were promulgated since
the MACT standards being reviewed in
this action. We reviewed the regulatory
requirements and/or technical analyses
associated with these regulatory actions
to identify any practices, processes and
control technologies considered in these
efforts that could be applied to emission
sources in the Aerospace Manufacturing
and Rework Facilities source category,
as well as the costs, non-air impacts and
energy implications associated with the
use of these technologies. Additionally,
we requested information from facilities
regarding developments in practices,
processes or control technology. Finally,
we reviewed information from other
sources, such as state and/or local
permitting agency databases and
industry-supported databases.
IV. Analytical Results and Proposed
Decisions
A. What actions are we taking pursuant
to CAA sections 112(d)(2) and
112(d)(3)?
We are not proposing any new
emissions limitations to the NESHAP
other than with respect to specialty
coatings. In this action, we are
proposing the following revisions to the
Aerospace NESHAP to ensure the
standards are consistent with the
requirements of the CAA as interpreted
by the courts: adding standards to limit
organic and inorganic HAP emissions
from specialty coating application
operations and updating the provisions
regulating emissions during periods of
SSM. Additionally, we are adding an
alternative compliance demonstration
provision for all types of coating
application operations (primers,
topcoats, specialty coatings and
chemical milling maskants) in certain
situations. The results and proposed
decisions based on the analyses
performed pursuant to CAA section
112(d)(2) and (3) are presented below.
We are proposing to establish MACT
standards specific to specialty coating
application operations to ensure the
standards are consistent with the
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requirements of the CAA as interpreted
by the courts. Under CAA section
112(d)(3), the EPA is required to
promulgate emissions limits for all HAP
emitted from major source categories.29
Specialty coatings are a source of HAP
emissions from the Aerospace
Manufacturing and Rework Facilities
source category that is not currently
regulated under the Aerospace
NESHAP. We are proposing organic
HAP content limits to reduce organic
HAP emissions and equipment and
work practice standards to reduce
inorganic HAP emissions associated
with specialty coating application. Refer
to section IV.E.1 of this preamble for a
description of specialty coating
application operations, associated
emissions and how this emissions
source is addressed in the current
Aerospace NESHAP, and how the EPA
established the MACT floor for specialty
coating application operations. Section
IV.E.1 of this preamble also includes the
EPA’s rationale for proposing this
standard, as well as how the EPA
established the MACT floor for specialty
coating application operations and the
estimated costs for complying with the
proposed standard. The EPA is
proposing to add these standards for
specialty coatings because they are a
source of HAP emissions from the
Aerospace Manufacturing and Rework
Facilities source category and EPA had
not previously established MACT
standards for these emissions points.
These proposed changes are necessary
to ensure the emissions standards are
consistent with the requirements of the
CAA as interpreted by the courts and
are unrelated to the risk findings.
The EPA is also proposing to revise
the provisions affecting periods of SSM
to clarify that the emission limitations
in the Aerospace NESHAP apply at all
times, including during these SSM
periods. Refer to section IV.E.3 of this
preamble for a description of the EPA’s
proposed revisions to the SSM
provisions for aerospace manufacturing
and rework operations. These proposed
changes to the SSM provisions are
necessary to ensure the emissions
standards are consistent with the
requirements of the CAA as interpreted
by the courts and are unrelated to the
risk findings.
The EPA also collected emissions data
and performed a risk analysis for certain
emissions points outside of the source
category—chemical milling and metal
finishing operations, waste water
operations, storage tanks and composite
operations that are related to aerospace
manufacturing and rework, but are not
surface coating operations. The data
collected for these non-surface coating
operations were used to characterize the
risk presented from these operations in
order to estimate the total risk from the
entirety of each aerospace
manufacturing and rework facility. The
EPA is not proposing to expand the
Aerospace Manufacturing and Rework
Facilities source category to include
these operations, which are not surface
coating operations and were not part of
the original source category and which,
as explained below, did not present
unacceptable risks. The initial and
subsequent listings of source categories
for regulation under section 112 of the
CAA included Aerospace
Manufacturing and Rework Facilities
only as a surface coating source
category.30 31
B. What are the results of the risk
assessment and analyses?
1. Inhalation Risk Assessment Results
Table 2 of this preamble provides an
overall summary of the results of the
inhalation risk assessment.
TABLE 2—AEROSPACE MANUFACTURING AND REWORK FACILITIES INHALATION RISK ASSESSMENT RESULTS
Maximum
individual
cancer risk
(-in-1 million) a
Estimated
annual
cancer
incidence
(cases per
year)
Estimated
population at
increased risk
levels of cancer
Maximum
chronic
non-cancer
TOSHI b
Maximum screening acute non-cancer HQ c
Actual Emissions
10 ......................
≥ 1-in-1 million: 180,000 .......
≥ 10-in-1 million: 1,500
≥ 100-in-1 million: 0
0.02
0.5
HQREL = 2 (ethylene glycol ethyl ether acetate).
Allowable Emissions d
10 ......................
≥ 1-in-1 million: 180,000 .......
≥ 10-in-1 million: 2,000
≥ 100-in-1 million: 0
0.02
0.5
a Estimated
maximum individual excess lifetime cancer risk due to HAP emissions from the source category.
TOSHI. The target organ with the highest TOSHI for the Aerospace Manufacturing and Rework Facilities source category for both
actual and allowable emissions is the kidney system.
c See Section III.A.3 of this preamble for explanation of acute dose-response values. Acute assessments are not performed on allowable emissions.
d The development of allowable emission estimates can be found in the memorandum titled, Aerospace Manufacturing and Rework Facilities
RTR Modeling File Preparation, December 2014, which is available in the docket.
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b Maximum
The inhalation risk modeling
performed to estimate risks based on
actual and allowable emissions relied
primarily on emissions data from the
ICRs and calculations described in the
memorandum titled, Aerospace
29 For more details see the discussion of Sierra
Club v. EPA, 479 F. 3d 875 (D.C. Cir. 2007) in
section II.E of this preamble, which found that the
EPA may not set ‘‘no emissions reductions’’ MACT
floors.
30 Initial List of Categories of Sources Under
Section 112(c)(1) of the Clean Air Act Amendments
of 1990. 57 FR 31576, July 17, 1992.
31 National Emission Standards for Hazardous Air
Pollutants; Revision of Initial List of Categories of
Sources and Schedule for Standards Under Sections
112(c) and (e) of the Clean Air Act Amendments of
1990. 61 FR 28197, June 4, 1996.
32 See the EPA’s ‘‘Coatings and Composites
Coordinated Rule Development’’ Web page at
https://www.epa.gov/ttnatw01/coat/coat.html for a
full list of surface coating-related NESHAP, and
links to Web pages specific to each surface coating
NESHAP.
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Manufacturing and Rework Facilities
RTR Modeling File Preparation,
December 2014, which is available in
the docket for this action. The results of
the chronic baseline inhalation cancer
risk assessment indicate that, based on
estimates of current actual emissions,
the MIR posed by the Aerospace
Manufacturing and Rework Facilities is
10-in-1 million, with emissions of
strontium chromate, from coating
operations accounting for the majority
of the risk. The total estimated cancer
incidence from Aerospace
Manufacturing and Rework Facilities
based on actual emission levels is 0.02
excess cancer cases per year or one case
every 50 years, with emissions of
strontium chromate and chromium
compounds contributing 66 percent and
15 percent, respectively, to the cancer
incidence. In addition, we note that
approximately 1,500 people are
estimated to have cancer risks greater
than or equal to 10-in-1 million, and
approximately 180,000 people are
estimated to have risks greater than or
equal to 1-in-1 million as a result of
actual emissions from this source
category.
When considering MACT-allowable
emissions, the MIR is estimated to be up
to 10-in-1 million, driven by emissions
of strontium chromate from coating
operations. The estimated cancer
incidence is estimated to be 0.02 excess
cancer cases per year, or one excess case
in every 50 years. Approximately 2,000
people are estimated to have cancer
risks greater than or equal to 10-in-1
million and approximately 180,000
people are estimated to have cancer
risks greater than or equal to 1-in-1
million considering allowable emissions
from Aerospace Manufacturing and
Rework Facilities.
The maximum modeled chronic noncancer HI (TOSHI) value for the source
category based on actual emissions is
estimated to be 0.5, driven by cadmium
compounds emissions from blast
depainting. When considering MACTallowable emissions, the maximum
chronic non-cancer TOSHI value is
estimated to be 0.5, also driven by
cadmium compounds emissions from
blast depainting.
2. Acute Risk Results
Our screening analysis for worst-case
acute impacts based on actual emissions
indicates the potential for one pollutant,
ethylene glycol ethyl ether acetate, from
one facility, to have HQ values above 1,
based on its REL value. One hundred
forty-three of the 144 Aerospace
Manufacturing and Rework Facilities
had an estimated worst-case HQ less
than or equal to 1 for all HAP.
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To better characterize the potential
health risks associated with estimated
worst-case acute exposures to HAP from
the source category at issue and in
response to a key recommendation from
the SAB’s peer review of the EPA’s CAA
section 112(f) RTR risk assessment
methodologies, we examine a wider
range of available acute health metrics
than we do for our chronic risk
assessments. This is in
acknowledgement that there are
generally more data gaps and
inconsistencies in acute reference
values than there are in chronic
reference values.
By definition, the acute CalEPA REL
represents a health-protective level of
exposure, with no risk anticipated
below those levels, even for repeated
exposures; however, the health risk
from higher-level exposures is
unknown. Therefore, when a CalEPA
REL is exceeded and an AEGL–1 or
ERPG–1 level is available (i.e., levels at
which mild effects are anticipated in the
general public for a single exposure), we
have used them as a second comparative
measure. Historically, comparisons of
the estimated maximum off-site 1-hour
exposure levels have not been typically
made to occupational levels for the
purpose of characterizing public health
risks in RTR assessments. This is
because occupational ceiling values are
not generally considered protective for
the general public since they are
designed to protect the worker
population (presumed healthy adults)
for short-duration (less than 15-minute)
increases in exposure. As a result, for
most chemicals, the 15-minute
occupational ceiling values are set at
levels higher than a 1-hour AEGL–1,
making comparisons to them irrelevant
unless the AEGL–1 or ERPG–1 levels are
also exceeded.
The worst-case maximum estimated
1-hour exposure to ethylene glycol ethyl
ether acetate outside the facility fence
line for the source categories is 0.3 mg/
m3. This estimated worst-case exposure
exceeds the 1-hour REL by a factor of 2
(HQREL = 2). All other HAP in this
analysis have worst-case acute HQ
values of 1 or less (maximum HQAEGL¥1
= 0.02 for phenol, maximum HQERPG¥1
= 0.03 for phenol) indicating that they
carry no potential to pose acute
concerns.
In characterizing the potential for
acute non-cancer impacts of concern, it
is important to remember the upward
bias of these exposure estimates (e.g.,
worst-case meteorology coinciding with
a person located at the point of
maximum concentration during the
hour) and to consider the results along
with the conservative estimates used to
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develop peak hourly emissions as
described in the Modeling File
Preparation Memo (which is available in
the docket for this action) for a detailed
description of how the hourly emissions
were developed for this source category.
3. Multipathway Risk Screening Results
Results of the worst-case Tier I
screening analysis indicate that PB–
HAP emissions of cadmium compounds
or mercury compounds did not exceed
the screening emission rates. Neither
dioxins nor polycyclic aromatic
hydrocarbons (PAH) are emitted by any
source in the source category.
4. Environmental Risk Screening Results
As described in section III.A of this
preamble, we conducted a screeninglevel evaluation of the potential adverse
environmental risks associated with
emissions of the following
environmental HAP from the Aerospace
Manufacturing and Rework Facilities
source category: lead, mercury,
cadmium, HCl and HF.
In the Tier 1 screening analysis for
PB–HAP (other than lead compounds,
which were evaluated differently), the
individual modeled Tier 1
concentrations for mercury and
cadmium did not exceed any ecological
benchmark for any facility in the source
category. For lead compounds, we did
not estimate any exceedances of the
secondary lead NAAQS.
For HF and HCl, the average modeled
concentration around each facility (i.e.,
the average concentration of all off-site
data points in the modeling domain) did
not exceed the ecological benchmarks.
In addition, each individual modeled
concentration of HCl and HF (i.e., each
off-site data point in the modeling
domain) was below the ecological
benchmarks for all facilities.
5. Facility-Wide Risk Results
The facility-wide chronic MIR and
TOSHI were estimated based on
emissions from all sources at the
identified facilities (both MACT and
non MACT sources). The results of the
facility-wide assessment for cancer risks
indicate that 44 facilities with aerospace
manufacturing and rework processes
have a facility-wide cancer MIR greater
than or equal to 1-in-1 million. The
maximum facility-wide cancer MIR is
20-in-1 million, primarily driven by
arsenic and chromium (VI) compounds,
from internal combustion engines. The
maximum facility-wide TOSHI for the
source category is estimated to be 0.5,
primarily driven by emissions of
hexamethylene-1,6-diisocyanate from
specialty coatings operations.
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6. What demographic groups might
benefit from this regulation?
To examine the potential for any
environmental justice (EJ) issues that
might be associated with the source
category, we performed a demographic
analysis, which is an assessment of risks
to individual demographic groups, of
the population close to the facilities. In
this analysis, we evaluated the
distribution of HAP-related cancer risks
and non-cancer hazards from the
Aerospace Manufacturing and Rework
Facilities across different social,
demographic and economic groups
within the populations living near
facilities identified as having the highest
risks. The methodology and the results
of the demographic analyses are
included in a technical report, Risk and
Technology Review—Analysis of Socio-
Economic Factors for Populations Living
Near Aerospace Facilities, available in
the docket for this action.
The results of the demographic
analysis are summarized in Table 3 of
this preamble. These results, for various
demographic groups, are based on the
estimated risks from actual aerospace
manufacturing and rework emissions
levels for the population living within
50 km of the facilities.
TABLE 3—AEROSPACE MANUFACTURING AND REWORK FACILITIES DEMOGRAPHIC RISK ANALYSIS RESULTS
Nationwide
Total Population .........................................................................................................................
Population with
cancer risk at or
above 1-in-1
million due to
emissions from
aerospace facilities
Population
with chronic
hazard index
above 1 due
to emissions
from aerospace facilities
312,861,265
179,074
0
72
28
64
36
NA
NA
72
13
1
14
64
19
1.5
16
NA
NA
NA
NA
17
83
16
84
NA
NA
14
86
19
81
NA
NA
15
85
17
83
NA
NA
Race by Percent
White ..........................................................................................................................................
All Other Races .........................................................................................................................
Race by Percent
White ..........................................................................................................................................
African American .......................................................................................................................
Native American ........................................................................................................................
Other and Multiracial .................................................................................................................
Ethnicity by Percent
Hispanic .....................................................................................................................................
Non-Hispanic .............................................................................................................................
Income by Percent
Below Poverty Level ..................................................................................................................
Above Poverty Level ..................................................................................................................
Education by Percent
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Over 25 and without High School Diploma ...............................................................................
Over 25 and with a High School Diploma .................................................................................
The results of the Aerospace
Manufacturing and Rework Facilities
baseline risk assessment indicate that
emissions from the source category
expose approximately 180,000 people to
a cancer risk at or above 1-in-1 million
and no one is predicted to have a
chronic non-cancer TOSHI greater than
1.
The analysis indicates that the
percentages of the population exposed
to a cancer risk greater than or equal to
1-in-1 million and living within 50 km
of the 144 aerospace facilities is higher
for minority populations, 36-percent
exposed versus the national minority
population average of 28 percent. The
specific demographics of the population
within 50 km of the facilities indicate
potential disparities in certain
demographic groups, including the
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‘‘African American’’ and ‘‘Below the
Poverty Level.’’
C. What are our proposed decisions
regarding risk acceptability, ample
margin of safety and adverse
environmental effects?
1. Risk Acceptability
As noted in section II.A.1 of this
preamble, the EPA sets standards under
CAA section 112(f)(2) using ‘‘a two-step
standard-setting approach, with an
analytical first step to determine an
‘acceptable risk’ that considers all
health information, including risk
estimation uncertainty, and includes a
presumptive limit on MIR of
approximately 1 in 10 thousand.’’ 54 FR
38045, September 14, 1989. For the
Aerospace Manufacturing and Rework
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Facilities source category, we estimate,
based on both actual and allowable
emissions, an MIR of 10-in-1 million
driven by emissions of strontium
chromate from coating operations. We
estimate that, based on actual emissions,
about 1,500 people are estimated to
have cancer risks greater than or equal
to 10-in-1 million and, based on
allowable emissions, about 2,000 people
have cancer risks greater than or equal
to 10-in-1 million. We estimate that
approximately 180,000 people are
estimated to have risks greater than or
equal to 1-in-1 million based on both
actual and allowable emissions from
this source category. The total estimated
incidence of cancer for this source
category due to inhalation exposures,
based on both actual and allowable
emissions, is 0.02 excess cancer cases
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per year, or 1 case in 50 years. The
agency estimates that the maximum
chronic non-cancer TOSHI from
inhalation exposure, based on both
actual and allowable emissions, from
this source category, is 0.5, with
cadmium compounds emissions from
blast depainting accounting for the
majority of the TOSHI.
The multipathway screening analysis,
based upon actual emissions, indicates
that PB–HAP emissions of both
cadmium compounds and mercury
compounds did not exceed the
screening emission rates. Neither
dioxins nor PAH are emitted by any
source in the source category. In
evaluating the potential for
multipathway effects from emissions of
lead, modeled maximum annual lead
concentrations were compared to the
secondary NAAQS for lead (0.15 mg/m3).
Results of this analysis estimate that the
NAAQS for lead would not be exceeded
at any off-site locations.
The screening assessment of worstcase acute inhalation impacts from
baseline actual emissions indicates that
the worst-case maximum estimated 1hour exposure to ethylene glycol ethyl
ether acetate outside the facility fence
line exceeds the 1-hour REL by a factor
of 2 (HQREL = 2). This exceedance was
only predicted to occur in a remote,
non-inhabited area just adjacent to the
facility fence line for 2 hours a year. All
other HAP in this analysis have worstcase acute HQ values of 1 or less
(maximum HQAEGL¥1 = 0.02 for phenol,
maximum HQERPG¥1 = 0.03 for phenol)
indicating that they carry no potential to
pose acute concerns.
In determining whether risks are
acceptable for this source category, the
EPA considered all available health
information including any uncertainty
in risk estimates. Also, as noted above,
the agency estimated risk from both
actual and allowable emissions. While
there are uncertainties associated with
both the actual and allowable emissions,
we consider the allowable emissions to
be an upper bound, based on the
conservative methods we used to
calculate allowable emissions.
The risk results indicate that both the
actual and allowable inhalation cancer
risks to the individual most exposed are
no greater than approximately 10-in-1
million, which is considerably less than
the presumptive limit of acceptability
(i.e., 100-in-1 million). The maximum
chronic non-cancer hazard indices for
both the actual and allowable inhalation
non-cancer risks to the individual most
exposed of 0.5 is less than 1.
The maximum acute non-cancer HQ
for all pollutants was 2 based on the
REL for ethylene glycol ethyl ether
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acetate. This value was only predicted
to occur during 2 hours per year in a
remote location adjacent to a single
facility’s fenceline. All other acute risks
are estimated to be below a noncancer
HI threshold of 1.
The multipathway screening analysis
indicates that PB–HAP emissions did
not exceed the screening emission rates
for any compound evaluated.
Considering all of the health risk
information and factors discussed
above, including the uncertainties
discussed in section III.A.8 of this
preamble, the EPA proposes that the
risks at baseline are acceptable since the
cancer risks are well below the
presumptive limit of acceptability and
the non-cancer results indicate there is
minimal likelihood of adverse noncancer health effects due to HAP
emissions from this source category.
2. Ample Margin of Safety Analysis and
Proposed Controls
Under the ample margin of safety
analysis, we evaluate the cost and
feasibility of available control
technologies and other measures
(including the controls, measures and
costs evaluated under the technology
review) that could be applied in this
source category to further reduce the
risks due to emissions of HAP identified
in our risk assessment, as well as the
health impacts of such potential
additional measures. As noted in our
discussion of the technology review in
section III.C of this preamble, no
measures (beyond those already in place
or that we are proposing today under
CAA sections 112 (d)(2) and (d)(3)) were
identified for reducing HAP emissions
from the Aerospace Manufacturing and
Rework Facilities source category.
Therefore, we propose that the current
standards provide an ample margin of
safety to protect public health.
Although the current standards were
found to provide an ample margin of
safety to protect public health, we are
proposing additional standards under
CAA sections 112(d)(2) and (3) that
address previously unregulated
emissions of HAP from specialty coating
application operations. The additional
standards are being proposed to address
a deficiency in the Aerospace NESHAP
as discussed previously in section II.E.
of this preamble. We are proposing
organic HAP and volatile organic
compound (VOC) content limits for
specialty coatings that are equal to the
VOC content limits specified in the
Aerospace CTG for specialty coatings.
Facilities that do not use specialty
coatings and those in nonattainment
areas that are currently complying with
the Aerospace CTG limits for their
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specialty coating operations will not
have to do anything new to meet these
requirements. The 74 facilities located
in attainment areas that reported using
specialty coatings in the 2011 ICR may
not be using compliant coatings and
may need to use alternative coatings,
direct the emissions stream to an addon control device or use the averaging
option to demonstrate compliance with
implement the standards. We are also
proposing that specialty coating
application operations be subject to the
same equipment standards (i.e., use
high-efficiency application equipment)
currently required for primer and
topcoat application operations. Further,
we are proposing to require that
specialty coating application operations
meet current work practice standards for
primer and topcoat application
operations for inorganic HAP emissions.
The estimated emission reductions
resulting from these proposed HAP
content limits, equipment standards and
work practice standards for specialty
coatings are 58 tons of HAP per year. As
noted above, we are proposing that the
MACT standard, prior to the
implementation of these proposed
standards for specialty coatings,
provides an ample margin of safety to
protect public health. Therefore, we
maintain that, after the implementation
of these standards for specialty coatings,
the rule will continue to provide an
ample margin of safety to protect public
health. Consequently, based on current
information, we do not expect it will be
necessary to conduct another residual
risk review under CAA section 112(f) for
this source category 8 years following
promulgation of new emission limits
and equipment and work practice
standards for specialty coatings, merely
due to the addition of these MACT
requirements. While our decisions on
risk acceptability and ample margin of
safety are supported even in the absence
of these reductions for specialty
coatings, if we finalize the proposed
requirements for these sources, they
would further strengthen our
conclusions that risk is acceptable with
an ample margin of safety to protect
public health.
Although we did not identify any new
technologies, other than for specialty
coatings application operations, to
reduce risk for this source category, we
are specifically requesting comment on
whether there are additional control
measures that may be able to reduce
risks from the source category. We
request any information on potential
emission reductions of such measures,
as well the cost and health impacts of
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such reductions to the extent they are
known.
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3. Adverse Environmental Effects
Based on the results of our
environmental risk screening
assessment, we conclude that there is
not an adverse environmental effect as
a result of HAP emissions from the
Aerospace Manufacturing and Rework
Facilities source category. We are
proposing that it is not necessary to set
a more stringent standard to prevent,
taking into consideration costs, energy,
safety and other relevant factors, an
adverse environmental effect.
D. What are the results and proposed
decisions based on our technology
review?
As described in section III.C of this
preamble, our technology review
focused on identifying developments in
practices, processes and control
technologies for the Aerospace
Manufacturing and Rework Facilities
source category. The EPA reviewed
various information sources regarding
emission sources that are currently
regulated by the Aerospace NESHAP,
which include primer and topcoat
application operations, maskant
application operations, cleaning
operations, chemical and blast
depainting operations and waste storage
and handling operations.
For the technology review, we
conducted a search of the EPA’s RACT/
BACT/LAER Clearinghouse (RBLC) and
regulatory actions (MACT standards,
area sources standards and residual risk
standards) subsequent to promulgation
of the 1995 Aerospace NESHAP.32 We
reviewed Washington State’s records of
Prevention of Significant Deterioration
(PSD) permits. Further, we considered
numerous relevant regional and state
regulations (e.g., California, Missouri,
Delaware and Arizona), the Ozone
Transport Commission serving the
Northeastern United States and state
implementation plans. We reviewed the
database of responses to the 2011 ICR to
determine the technologies and
practices reported by industry.
We reviewed these sources for
information on add-on control
technologies, other process equipment,
work practices and procedures and
process changes or pollution prevention
alternatives that were not considered
during development of the Aerospace
NESHAP. We also looked for
32 See the EPA’s ‘‘Coatings and Composites
Coordinated Rule Development’’ Web page at
https://www.epa.gov/ttnatw01/coat/coat.html for a
full list of surface coating-related NESHAP, and
links to Web pages specific to each surface coating
NESHAP.
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information on improvements in add-on
control technology, other process
equipment, work practices and
procedures and process changes or
pollution prevention alternatives that
have occurred since development of the
Aerospace NESHAP. Regarding process
changes or pollution prevention
alternatives, we searched for
advancements in the use of low-HAP
coatings and solvents, advancements in
the use of high solids coatings and the
adoption of lower VOC content limits
for coatings and solvents.
The following sections summarize our
technology review results for each of
these emission sources.
1. Primer and Topcoat Application
Operations
As defined in the Aerospace NESHAP
(see 40 CFR 63.742), a coating is a
material that is applied to the surface of
an aerospace vehicle or component to
form a decorative or functional solid
film, or the solid film itself. A primer is
the first layer and any subsequent layers
of coating prior to the topcoat and is
typically used for corrosion prevention,
protection from the environment,
functional fluid resistance and adhesion
of subsequent coatings. A topcoat is a
coating that is applied over one or more
layers of a primer for appearance,
identification, camouflage or protection.
Specialty coatings are not included in
the categories of primers or topcoats
currently subject to regulation under 40
CFR 63.745.
Most aerospace coatings contain a
mixture of organic solvents that may be
HAP, and also inorganic pigments, such
as various metal compounds, which
may also be HAP. The organic HAP
emissions from the application of
primers and topcoats occur from the
evaporation of organic solvents during
mixing, application and drying.
Emissions of inorganic HAP from sprayapplied coating operations, typically
metal compounds (e.g., chromium,
cadmium compounds), occur when
coating particles do not adhere to the
surface being coated (i.e., overspray).
The organic and inorganic emissions
from coating application occur in large
open areas, such as hangars or in
partially or fully enclosed spaces, such
as within spray booths.
The existing Aerospace NESHAP
requires the following organic HAP and
VOC content limits for uncontrolled
primers and topcoats (40 CFR
63.745(c)):
• Primers: 2.9 lb/gal (less water) as
applied; or 4.5 lb/gal (less water) as
applied for general aviation rework
facilities, or 5.4 lb/gal (less water) as
applied, to large commercial aircraft
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components (parts or assemblies) or
fully assembled, large commercial
aircraft.
• Topcoats: 3.5 lb/gal (less water) as
applied; or 4.5 lb/gal (less water) as
applied for general aviation rework
facilities.
Alternatively, a control system can be
used to capture and control organic
HAP and VOC emissions from the
primer or topcoat application
operations. The system must achieve an
overall control efficiency of 81 percent
of organic HAP and VOC emissions (40
CFR 63.745(d)).
In addition, the Aerospace NESHAP
requires the use of one of the following
coating application techniques (40 CFR
63.745(f)):
• Flow/curtain coat application.
• Dip coat application.
• Roll coating.
• Brush coating.
• Cotton-tipped swab application.
• Electrodeposition (dip) coating.
• High volume low pressure (HVLP)
spraying.
• Electrostatic spray application.
• Other coating application methods
that achieve emission reductions
equivalent to HVLP or electrostatic
spray application methods.
The Aerospace NESHAP also includes
operating requirements for the
application of primers or topcoats that
contain inorganic HAP, including
control of spray booth exhaust streams
with either particulate filters or
waterwash spray booths (40 CFR
63.745(g)).
Based on the technology review for
primers and topcoats, we did not
identify any practices, processes or
control technologies beyond those
already required by the Aerospace
NESHAP. A brief summary of the EPA’s
findings in conducting its RTR review of
primer and topcoat application
operations follows. For a detailed
discussion of the EPA’s findings, refer to
the memorandum, Technology Review
for Primer and Topcoat Application
Operations in the Aerospace Source
Category, January 2015, available in the
docket for this action.
In reviewing add-on control
technologies or other equipment and
work practices and procedures, we did
not identify any add-on control
technologies, other equipment or work
practices and procedures that had not
previously been considered during
development of the Aerospace NESHAP,
nor did we identify any developments
in the same since the promulgation of
the NESHAP.
Based on our search of the RBLC, we
did not find any more stringent
requirements. We identified one facility
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in Washington State, for which a Best
Achievable Control Technology (BACT)
analysis was completed in September
2014, for constructing new buildings
needed for producing new models of
large commercial airplanes, including
the building and surface coating of
composite aircraft wings. The surface
coating operations on these aircraft
wings would involve the use of primers
and topcoats that are subject to the
limits in 40 CFR 63.745. The BACT
analysis concluded that there are no
demonstrations of add-on controls at
facilities performing surface coating
comparable to large commercial aircraft
wing components. The analysis also
concluded that add-on controls would
not be cost effective for surface coating
of large components, such as wings,
much less fully assembled large
commercial aircraft.
In reviewing improvements in add-on
control technologies or other equipment
that had previously been considered
during development of the Aerospace
NESHAP, specifically in conducting a
technology review of the wood
manufacturing industry, we found that
the Wood Furniture Manufacturing
NESHAP, 40 CFR part 63, subpart JJ,
requires the use of high-efficiency spray
guns (e.g., airless spraying, air assisted
airless spraying, electrostatic spraying
and HVLP spray guns) and prevents the
use of conventional spray guns.
Although the Aerospace NESHAP does
not specifically prohibit the use of
conventional spray methods, it does
specify that only spray application
methods that are equivalent to HVLP or
electrostatic spray application methods
may be used. Because conventional
spray guns can be used only if they can
achieve the same efficiency as HVLP or
electrostatic spray application methods,
the Aerospace NESHAP and the Wood
Furniture Manufacturing NESHAP are
essentially equivalent. No other new
developments in add-on control
technologies or other equipment were
found.
The EPA reviewed the 2011 ICR data
for advancements in the use of low-HAP
liquid primers and topcoats as process
changes and pollution prevention
alternatives that could be transferred to
and used in this source category and
that were not identified and considered
during development of the Aerospace
NESHAP. In this review, we found some
facilities with weighted-average HAP
content values below the HAP and VOC
content limits for primers and topcoats
in the Aerospace NESHAP. However,
the data collected by the ICR cannot be
compared directly with the HAP and
VOC content limits in the Aerospace
NESHAP because the NESHAP limits
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are based on grams of HAP per liter of
coating, less water. The ICR asked for
readily available data, such as data from
product sheets and material safety data
sheets, which did not provide data on
the water content of the coatings. As a
result, we cannot accurately convert the
reported HAP contents from the ICR to
the same basis as in the Aerospace
NESHAP. Moreover, we believe that if
the coatings in the ICR contained water
and the water content of the coatings is
removed, then the corrected HAP
content of the coatings would increase
and the apparent difference between the
ICR data and the NESHAP limits would
be reduced.
Finally, many of the currently used
coatings have already been reformulated
to meet the current MACT HAP content
limits. Manufacturers of aerospace
vehicles are constrained to using certain
types of primers and topcoats based on
the market segment for which the
coating is intended (i.e., military
original equipment manufacturer
(OEM), military rework, commercial
OEM or commercial rework) and the
unique circumstances and design
considerations within each market
segment. In addition to being regulated
by the Aerospace NESHAP, aerospace
vehicle manufacturing and rework
operations are also regulated by the
Federal Aviation Administration (FAA),
the Department of Defense and specific
customer requirements. As outlined in
the EPA’s 1998 promulgation of
amendments to the Aerospace
NESHAP,33 affected sources must
comply with FAA Airworthiness
Directives (AD) that can potentially
require the use of chemicals containing
HAP, and affected sources may have to
obtain alternative means of compliance
for AD to allow for the substitution of
non-HAP materials. These multiple
regulations can result in lengthy
processes for qualifying new paint
systems.
Based on a finding of no new
developments in practices, processes
and control technologies in the
technology review for primer and
topcoat application operations, we are
not proposing to revise the Aerospace
NESHAP HAP and VOC content limit
requirements for primer and topcoat
application operations pursuant to CAA
section 112(d)(6). For further discussion
of the technology review results, refer to
the memorandum, Technology Review
for Primer and Topcoat Application
Operations in the Aerospace Source
Category, January 2015, available in the
docket for this action.
33 63
PO 00000
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2. Chemical Milling Maskant
Application Operations
In the process of chemical milling, an
etchant solution is used to chemically
reduce the thickness of selected areas of
metal parts. The process is typically
used when the size or shape of the part
precludes mechanical milling or when
chemical milling is advantageous due to
shorter processing time or its batch
capability. Before chemical milling, a
maskant is applied to the part, allowed
to cure and is then removed from
selected areas of the part where metal is
to be removed by the etchant. The
maskant remaining on the part protects
those areas from the etchant. Maskants
are applied by brushing, dipping,
spraying or flow coating. Organic HAP
emissions occur through evaporation of
the solvent in the maskant, typically
toluene, xylene or perchloroethylene, as
the maskant is applied and while it
cures.
There are two subcategories of
chemical milling maskants in the
Aerospace NESHAP. Type I maskants
are used with chemical milling etchants
that contain dissolved sulfur and no
amines, and Type II maskants are used
with etchants that are strong sodium
hydroxide solutions containing amines.
The Aerospace NESHAP requires the
following organic HAP and VOC content
limits for uncontrolled chemical milling
maskants (40 CFR 63.747(c)):
• Type I: 5.2 pounds organic HAP per
gallon (622 g/L) less water, as applied.
• Type II: 1.3 pounds of organic HAP
per gallon (160 g/L) less water, as
applied.
These requirements do not apply to
touch-up of scratched surfaces or
damaged maskant and touch-up of
trimmed edges. Alternatively, a control
system can be used to capture and
control emissions from the maskant
application operation. The system must
achieve an overall control efficiency of
81 percent (40 CFR 63.747(d)).
Based on the technology review for
chemical milling maskants, we did not
identify any add-on control
technologies, other equipment or work
practices and procedures that had not
previously been considered during
development of the Aerospace NESHAP.
Additionally, we did not identify any
improvements that could be transferred
to this source category. In our search of
the RBLC, we also did not find any more
stringent requirements. We did find that
some California air quality management
districts require more stringent VOC
content limits than those in the
Aerospace NESHAP and have higher
overall minimum control requirements
for the use of add-on control technology.
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However, the EPA did not find any
chemical milling maskant application
operations located in these two districts
that are subject to these more stringent
limits.
Based on a finding of no new
developments in practices, processes
and control technologies in this
technology review, we are not proposing
revisions to the Aerospace NESHAP for
chemical milling maskant application
operations pursuant to CAA section
112(d)(6). Refer to the memorandum,
Technology Review for Chemical Milling
Maskant Application Operations in the
Aerospace Source Category, January
2015, available in the docket for this
action, for more a more detailed
description of the technology review
results.
3. Cleaning Operations
At Aerospace Manufacturing and
Rework Facilities, cleaning operations
are used at essentially every processing
step of aerospace surface coating, from
preparing surfaces to be coated to
cleaning the coating application
equipment. The cleaning operations
regulated by the current Aerospace
NESHAP include hand-wipe cleaning,
spray gun cleaning and flush cleaning,
as well as housekeeping measures for
storage, handling and transfer of
cleaning solvents and solvent-laden
materials.
The liquid cleaning solutions used in
cleaning operations for the aerospace
industry contain organic solvents, and
some of these organic solvents are HAP.
Organic HAP emissions from the
cleaning operations are often fugitive in
nature, resulting from the evaporation of
the volatile portion of the cleaning
solvent in large open areas, such as
hangars. They may also be emitted from
stacks when the solvents are used in
partially or fully enclosed spray booths
that are ventilated through stacks.
The current Aerospace NESHAP
requires that hand-wipe and flush
cleaning solvents meet certain
composition requirements, or that the
cleaning solvents have a composite
vapor pressure of no more than 45 mm
Hg (24.1 inches water) (40 CFR
63.744(b) and (d)). The NESHAP
specifies work practice standards for
spray gun cleaning (e.g., cleaning a
spray gun in an enclosed gun cleaning
system) and flush cleaning operations
(e.g., for flush cleaning events, empty
used cleaning solvent into an enclosed
container) (40 CFR 63.744(c) and (d)).
Work practice measures are also
specified for the storage and handling of
solvents and solvent-laden materials
(e.g., solvent-laden cloth, paper or other
absorbent materials) (40 CFR 63.744(a)).
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Based on the technology review for
cleaning operations, we did not identify
any practices, processes or control
technologies beyond those already
required by the Aerospace NESHAP that
could be transferred to the source
category. A brief summary of the EPA’s
findings in conducting its RTR review of
cleaning operations follows. For a
detailed discussion of the EPA’s
findings, refer to the memorandum,
Technology Review for Cleaning
Operations in the Aerospace Source
Category, January 2015, available in the
docket for this action.
In the technology review, we did not
identify any improvements in add-on
control technologies, other equipment
or work practices and procedures since
promulgation of the Aerospace
NESHAP. The EPA identified one
aerospace manufacturing and rework
facility that routes the air flow from a
spray booth to a carbon adsorption
control device when performing spray
gun cleaning and residual spray gun
hand-wipe cleaning. We found that this
was the same spray booth in which
surface coating is performed, and it is
not a spray booth dedicated to spray gun
cleaning. Based on the results of the
responses to the EPA’s 2011 information
collection survey for other facilities, the
EPA concluded that this practice could
not be applied to the source category
without impacting facility operations.
First, very few facilities have carbon
adsorbers controlling emissions from
spray booths. Second, it is not always
practical to move the spray gun cleaning
operations into a spray booth without
affecting the surface coating operations
in that spray booth because of space
limitations within the booth.
The EPA also identified one aerospace
manufacturing and rework facility that,
for certain cleaning operations, uses a
non-HAP solvent blend that has a vapor
pressure of 36 mm Hg for certain
cleaning operations; the facility does not
use this solvent for all cleaning
operations. The use of non-HAP
cleaning solvent is already a compliance
option that was considered in the
development of the Aerospace NESHAP
and is included in 40 CFR 63.744.
Based on a finding of no new
developments in practices, processes
and control technologies in the
technology review, we are not proposing
any revisions to the Aerospace NESHAP
standard requirements for cleaning
operations pursuant to CAA section
112(d)(6). For further discussion of the
technology review results, refer to the
memorandum, Technology Review for
Cleaning Operations in the Aerospace
Source Category, January 2015, available
in the docket for this action.
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4. Chemical and Dry Media Blasting
Depainting Operations
At Aerospace Manufacturing and
Rework Facilities, chemical and dry
media blasting depainting operations
remove unwanted or old surface
coatings (e.g., primers, topcoats and
specialty coatings) to prepare the
surface for painting. As defined in the
Aerospace NESHAP, a depainting
operation means the use of a chemical
agent, media blasting or any other
technique to remove permanent coatings
from the outer surface of an aerospace
vehicle or components, excluding hand
and mechanical sanding or other nonchemical removal processes that do not
involve blast media or other
mechanisms that would result in
airborne particle movement at high
velocity. The depainting operation
includes washing of the aerospace
vehicle or component to remove
residual stripper, media or coating
residue. Depainting is most often done
in the rework of existing aircraft, but
may also be done in limited
circumstances in the manufacture of
new aircraft.
The liquid chemical agents (i.e.,
strippers) used to remove permanent
coatings in the aerospace industry
contain organic solvents. Organic HAP
emissions from strippers occur from the
evaporation of the chemical stripper
during mixing, application and possibly
during washing of the vehicle or
component to remove residual stripper.
The organic emissions from depainting
operations that occur within a booth or
hangar are typically captured and
exhausted through a stack, although
some emissions may be fugitive in
nature (e.g., open containers of stripper).
Inorganic HAP, typically metal
compounds (e.g., compounds of lead,
chromium or cadmium), can be emitted
during dry media blasting if these
compounds are present in the paint
layer that is being removed. These
inorganic HAP would be emitted as
particulate matter as the dry media
blasting removes the existing coating
through abrasion.
The Aerospace NESHAP restricts
facilities to using organic HAPcontaining chemical strippers for only
spot stripping and decal removal. The
amount of stripper used for spot
stripping and decal removal is limited
to no more than 26 gallons of HAPcontaining chemical stripper (or
alternatively 190 pounds of organic
HAP) for each commercial aircraft, and
50 gallons (or 365 pounds of organic
HAP) for each military aircraft. As an
alternative, facilities may use controls
for organic HAP emissions from
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chemical depainting, and emissions
must be reduced by 81 percent for
controls installed before the effective
date, and by 95 percent for controls
installed on or after the effective date
(40 CFR 63.746(b)(1) through (3) and
(c)).
For non-chemical depainting
operations that generate inorganic HAP
emissions from dry media blasting, the
operation must be performed in an
enclosed area or in a closed cycle
depainting system and the air stream
from the operation must pass through a
dry filter system meeting a minimum
efficiency specified in the rule, through
a baghouse or through a waterwash
system before being released to the
atmosphere (40 CFR 63.746(b)(4)).
Based on the technology review for
depainting operations, we did not
identify any practices, processes or
control technologies that were not
already required by the Aerospace
NESHAP or considered in its
development, nor did we identify any
improvements to those practices,
processes or control technologies that
could be transferred and applied to this
source category. A brief summary of the
EPA’s findings in conducting the RTR
review of chemical and dry media blast
depainting operations follows. For a
detailed discussion of the EPA’s
findings, refer to the memorandum,
Technology Review for Depainting
Operations in the Aerospace Source
Category, January 2015, available in the
docket for this action.
In reviewing Washington State’s
records of permits for Aerospace
Manufacturing and Rework Facilities,
we identified a 2013 PSD permit
amendment that requires the VOC vapor
pressure of cleaning solvents and
chemical strippers used in depainting
operations to be less than 45 mm Hg.
The Aerospace NESHAP does not
prescribe vapor pressure limits to
chemical depainting strippers, but
instead has capture and control and
volume usage limits for chemical
depainting operations that use HAPcontaining chemical strippers.
Otherwise, facilities must use non-HAP
chemical strippers. Therefore, we
believe that the Aerospace NESHAP is
at least as stringent as the Washington
State PSD permit requirements.
Based on a finding of no new
developments in practices, processes
and control technologies in the
technology review, we are not proposing
to revise the Aerospace NESHAP
standard requirements for chemical or
dry media blast depainting operations
pursuant to CAA section 112(d)(6). For
further discussion of the technology
review results, refer to the
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memorandum, Technology Review for
Depainting Operations in the Aerospace
Source Category, January 2015, available
in the docket for this action.
5. Waste Storage and Handling
Operations
At Aerospace Manufacturing and
Rework Facilities, waste is produced
primarily from cleaning, coating and
depainting operations. Cleaning
operations produce solvent-laden cloth
and paper and spent solvent which can
emit organic HAP from the evaporation
of the solvents. Coating operations
produce waste paint and waste solvent
that also emit organic HAP through
evaporation.
Depainting operations can produce
either a liquid or solid waste stream
depending on the type of process used.
Chemical depainting processes produce
a waste sludge that consists of the
stripper solution and paint residue.
Emissions occur from the evaporation of
the solvent from the stripper solution in
the waste sludge.
Blast depainting processes produce a
solid waste stream that consists of paint
chips and particles and spent blasting
media. Emissions do not directly occur
from this waste stream, although
particulate emissions are generated
during the blasting process.
The requirements for waste storage
and handling in the Aerospace NESHAP
apply to each waste storage and
handling operation, which is defined as
the total of all waste handling and
storage at the facility. In 40 CFR 63.748,
the Aerospace NESHAP requires that all
waste must be handled and transferred
to or from containers, tanks, vats,
vessels and piping systems in such a
manner that spills are minimized.
Because the EPA did not want to
create possible conflicts over the
handling of waste between the
Aerospace NESHAP and regulations
under the Resource Conservation and
Recovery Act (RCRA) of 1976 (Pub. L.
94–580), as implemented by 40 CFR
parts 260 and 261, the Aerospace
NESHAP specifically exempted wastes
covered under the RCRA regulations.34
Per 40 CFR 63.741(e), all wastes that are
determined to be hazardous wastes
under RCRA as implemented by 40 CFR
parts 260 and 261, and that are subject
to RCRA requirements as implemented
in 40 CFR parts 262 through 268, are
exempt from the requirements of the
Aerospace NESHAP.
The practical effect of the provisions
in 40 CFR 63.741(e) is that all HAPcontaining wastes generated by
34 See the preamble to the proposed rule, 59 FR
29216, June 6, 1994.
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aerospace manufacturing and rework
operations are subject to RCRA and are
exempt from the requirements of 40 CFR
63.748. Because all of these HAPcontaining wastes are covered under
RCRA and exempt from 40 CFR 63.748,
there is no need to do a technology
review for the standards for handling
and storage of waste.
E. What other actions are we proposing?
In addition to the proposed actions
described above, we are proposing
additional revisions. As stated
previously in this preamble, the United
States Court of Appeals for the District
of Columbia Circuit found that the EPA
had erred in establishing emissions
standards for sources of HAP in the
NESHAP for Brick and Structural Clay
Products Manufacturing and Clay
Ceramics Manufacturing, 67 FR 26690
(May 16, 2003), and consequently
vacated the rules.35 Among other things,
the court found EPA erred by failing to
regulate processes that emitted HAP, in
some instances by establishing a MACT
floor of ‘‘no control.’’ In this action we
are proposing to correct the same error
in the Aerospace NESHAP by proposing
to remove the exemption for specialty
coatings found at 40 CFR 63.741(f) and
instead add limits for specialty coatings
(including adhesives, adhesive bonding
primers and sealants).
1. Specialty Coating Application
At Aerospace Manufacturing and
Rework Facilities, specialty coatings are
those coatings that have additional
performance criteria for specific
applications that are beyond the criteria
for primers, topcoats and self-priming
topcoats, although specialty coatings
may still meet the definition of a primer
or topcoat. These additional
performance criteria may include, for
example, temperature or fire resistance,
substrate compatibility, antireflection,
temporary protection or marking,
sealant properties, adhesive properties,
electrical insulation, lubrication or
enhanced corrosion protection (40 CFR
63.742).
Specialty coatings contain a mixture
of organic solvents and/or inorganic
HAP. The organic HAP emissions from
the application of specialty coatings
occur from the evaporation of organic
solvents during mixing, application and
drying. Emissions of inorganic HAP
from spray-applied coating operations,
typically metal compounds (e.g.,
chromium, cadmium compounds),
occur when particles do not adhere to
the surface being coated (i.e.,
35 Sierra Club v. EPA, 479 F. 3d 875 (D.C. Cir.
March 13, 2007).
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overspray). The organic and inorganic
emissions from coating application
operations occur in large open areas,
such as hangars or partially or fully
enclosed spaces, such as within spray
booths.
The current Aerospace NESHAP
explicitly excludes specialty coatings
from meeting any control requirements,
as specified in 40 CFR 63.741(f) and in
40 CFR 63.742 (i.e., the definitions for
‘‘exterior primer,’’ ‘‘primer,’’ and
‘‘topcoat’’). Appendix A of the
Aerospace NESHAP defines 59 separate
categories of specialty coatings.
Although the EPA did not include
emission limitations for specialty
coatings in the Aerospace NESHAP
finalized in 1995 or in any subsequent
amendments, the EPA included VOC
content limits for the 59 categories of
specialty coatings in the 1997 Aerospace
CTG. The Aerospace CTG is intended to
provide state and local air pollution
control authorities with an information
base, recommended emissions
limitations and monitoring,
recordkeeping and reporting
requirements for proceeding with their
analyses of reasonably available control
technology (RACT) for their own
regulations to reduce VOC emissions
from aerospace surface coating
operations. The Aerospace CTG
includes presumptive VOC limits for
specialty coating operations that are
based on a review of the contemporary
knowledge and data concerning the
technology, impacts and costs
associated with various emission
control techniques. During their
development, the specialty coating
categories and VOC limits in the CTG
were also subject to a period of public
comment and review, and the final CTG
categories and VOC limits were revised
after proposal to reflect the EPA’s
analysis of those comments on the
proposed CTG.
In this action, we are proposing to
establish standards for specialty
coatings. Based on a MACT analysis for
specialty coatings, we are proposing to
require aerospace manufacturing and
rework specialty coating application
operations to achieve organic HAP
content limits that are equivalent to the
VOC content limits for specialty
coatings included in the Aerospace
CTG. As discussed previously in section
IV.E.1 of this preamble, the Aerospace
CTG may be adopted by state and local
agencies in nonattainment areas to assist
them in meeting their state
implementation plan requirements. Of
the 109 facilities that reported the use
of specialty coatings, 35 are in
nonattainment areas and likely
currently complying with the specialty
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coating limits in the Aerospace CTG.
The remaining facilities would need to
take action to comply with the specialty
coating application operations limits.
In the MACT analysis for specialty
coatings, the EPA considered data
provided in response to a
comprehensive information collection
request (ICR) sent out in February 2011
and consulted the EPA’s RACT/BACT/
LAER Clearinghouse, the California
Statewide Best Available Control
Technology (BACT) Clearinghouse and
regional and state regulations for
sources of data on control technologies
and limitations. We reviewed state rules
to compare the VOC limits in those
rules to the VOC limits in the Aerospace
CTG. This review of state rules was in
addition to a review of the database of
responses to the 2011 ICR and the RBLC
for information on add-on control
technology or other equipment, work
practices and procedures and process
changes or pollution prevention
alternatives not identified and
considered during development of the
Aerospace CTG, or improvements in the
same since the CTG development. A
brief summary of the EPA’s findings in
conducting its MACT analysis of
specialty coating application operations
follows. For a detailed discussion of the
EPA’s findings, refer to the
memorandum, Maximum Achievable
Control Technology for Specialty
Coating Operations in the Aerospace
Source Category, January 2015, available
in the docket for this action.
For specialty coatings, where there
were sufficient data, the EPA compared
the emissions for the best performing
coatings with the Aerospace CTG limits.
The results of this comparison showed
that the CTG VOC limits were
equivalent in performance to the best
performing specialty coating. Therefore,
we determined that the current
Aerospace CTG limits represent MACT
for specialty coatings.
Based on the results of the MACT
analysis, we determined that the VOC
limits in the Aerospace CTG for
specialty coatings are currently being
achieved by about half of all operating
sources subject to the Aerospace
NESHAP. The facilities complying with
the CTG limits for specialty coatings are
located in ozone non-attainment areas
where state VOC rules have been
developed based on the Aerospace CTG.
From our review of industry responses
to the 2011 ICR, we determined that
some facilities complying with these
state VOC limits employ use of add-on
control devices to reduce organic HAP
emissions (i.e., thermal oxidizers and
carbon adsorbers); however, these addon controls are not widely used in the
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source category. Other facilities achieve
equivalent emission reductions without
add-on controls by using coatings that
meet the VOC content limits.
Based on our review of state and
regional regulations for specialty coating
operations in the aerospace industry, we
identified several cases in which limits
are specified for certain specialty
coating categories that are lower than
the VOC content limits for the same
specialty coating categories in the
Aerospace CTG. These differences
generally affect about one-quarter of the
specialty coating categories (although
each state or regional regulation may
differ from the CTG in only a handful
of categories), and the limits differ by
less than 200 grams VOC per liter of
coating. However, these state and
regional rules and the Aerospace CTG
differ in certain ways, such that the
lower VOC limits in the state and
regional rules do not represent a more
stringent limit as compared to the
Aerospace CTG.
First, in many cases where a state rule
has a lower VOC limit than the CTG, the
state rule has also added coating
categories with VOC limits equal to or
higher than the CTG limits. For
example, one state rule has a lower limit
for fuel tank coatings, but has an
additional category for ‘‘rapid cure’’ fuel
tank coatings that is the same as the
CTG VOC limit.
Second, not all categories of specialty
coatings are used at all Aerospace
Manufacturing and Rework Facilities.
For the specialty categories with more
stringent VOC limits, the EPA does not
have data to confirm that facilities exist
in those jurisdictions that are using
those coatings and actually have to
comply with the more stringent VOC
limits. These data on facilities actually
using coatings subject to these more
stringent limits would be needed to
confirm that these more stringent limits
constitute the MACT floor according to
section 112(d)(3) of the CAA.
Finally, many of the areas with more
stringent VOC limits than in the CTG
have climates that are warmer and drier
than in most other parts of the United
States, and this type of climate is more
conducive to the use of low-VOC
coatings because it helps promote
expeditious curing of the coatings under
ambient conditions. In cooler and more
humid areas, the coatings require the
use of a solvent carrier and/or thermal
curing. The Aerospace NESHAP and
CTG, on the other hand, must establish
HAP and VOC limits that are applicable
across the United States. It is not
practical to establish MACT limits for
coatings based on regional climate
differences for this source category.
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Based on the issues noted above, the
EPA concludes that the noted
differences between the state and
regional rules and the Aerospace CTG
limits do not constitute more stringent
limits compared to those in the
Aerospace CTG. The EPA does not have
sufficient data to determine whether
these differences in VOC limits,
compared to the limits in the Aerospace
CTG, actually constitute MACT.
Therefore, the EPA is specifically
soliciting comment and additional data
on the differences noted between state
and regional rules and the aerospace
CTG.
Based on its analysis, the EPA is
proposing the MACT floor for specialty
coatings to be organic HAP content
limits equal to the VOC limits specified
in the Aerospace CTG for specialty
coatings. Additionally, the low-volume
exemption provisions in the current
Aerospace NESHAP for primers,
topcoats and chemical milling maskants
may be used for specialty coatings. The
EPA has not identified any options more
stringent than the MACT floor as
documented in the review of specialty
coatings discussed earlier in this
section, so the proposed organic HAP
content limits are equal to the MACT
floor VOC content limits. The EPA is
proposing this MACT floor based on the
fact that these VOC limits are currently
being achieved by at least 12 percent of
the operating facilities in a total
population of 109 operating aerospace
and rework facilities that reported using
specialty coatings in the 2011 ICR. For
more information on the MACT floor
analysis, please refer to the
memorandum, Maximum Achievable
Control Technology for Specialty
Coating Operations in the Aerospace
Source Category, January 2015, available
in the docket for this action.
In reviewing the state and district
VOC rules, the EPA determined that the
aerospace surface coating rules in many
of the California district rules, in
addition to the requirement to meet
VOC limits, require that all sprayapplied coating operations use highefficiency application equipment (i.e.,
HVLP, electrostatic spray or an
equivalent). This requirement is more
stringent than the model rule found in
the Aerospace CTG, which exempts
specialty coatings from the requirement
to use high-efficiency application
equipment. The California rules
examined by the EPA require the use of
high-efficiency application equipment
for all spray applied coatings, unless an
add-on control system was used, or
certain other exemptions apply. Other
state rules that follow the CTG require
high-efficiency application methods
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only for primer and topcoat application
operations. The facilities located in
California that are required to use highefficiency application equipment for
specialty coatings constitute the MACT
floor for the application of these
coatings. This determination is based on
the fact that at least 11 facilities in
California’s air pollution control
districts are currently subject to district
rules that require high-efficiency
application equipment for all coating
operations, including specialty coatings.
Therefore, the EPA is proposing that
specialty coatings be subject to the same
application requirements in 40 CFR
63.745(f) as primers and topcoats.
Compared to conventional spray
application methods, high-efficiency
application methods, such as HVLP
spray guns or electrostatic deposition,
can achieve HAP and VOC emission
reductions because of reduced coating
consumption that results from reduced
coating overspray. The EPA has not
identified any control options more
stringent than the use of high-efficiency
application methods for spray-applied
coating operations.
In our review of the RBLC, we did not
identify any control options for
aerospace specialty surface coating
operations that were not already
reflected in the VOC content limits in
the Aerospace CTG. However, we
identified one facility in the state of
Washington for which a BACT analysis
was completed in September 2014, for
constructing new buildings needed for
producing new models of large
commercial airplanes, including the
building and surface coating of
composite aircraft wings. The BACT
analysis described the facility as
currently using HVLP spraying and
electrostatic airless and modified highefficiency air-assisted airless spray
equipment in all spray applied surface
coating operations. The BACT analysis
concluded that there were no
demonstrations of add-on controls at
facilities performing surface coating
comparable to large commercial aircraft
wing components.
In our review of Washington State’s
record of permits, we determined that
the current PSD permit for this facility
identified BACT for VOC from coating
operations to be the equivalent of
complying with ‘‘all applicable VOC
emission standards of the Aerospace
NESHAP.’’ The PSD permit for the
facility did not consider add-on control
technologies to be BACT after taking
into account energy, environmental and
economic impacts. Based on this
information from the RBLC and the
Washington State BACT analysis, we
determined that add-on control
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techniques would not be MACT for
specialty coating application operations
for the aerospace industry.
Instead, MACT is being proposed as
the use of low-HAP coatings (with HAP
content limits equal to the VOC content
limits in the Aerospace CTG) and highefficiency application methods for
spray-applied coating operations. As the
EPA did with primers and top coats in
the current NESHAP, the EPA is
proposing to use VOC limits that are
currently in effect as the basis for
proposed organic HAP limits.
The EPA is also proposing to establish
MACT to limit emissions of inorganic
HAP from spray-applied specialty
coatings that contain inorganic HAP.
The predominant method used to
control inorganic HAP emissions from
all spray-applied coating operations
(including specialty coatings) is the use
of a spray booth with a particulate filter,
which generally achieves a high (i.e.,
greater than 99 percent) control
efficiency. The Aerospace NESHAP
currently requires the use of spray
booths with filters meeting minimum
efficiency requirements for the spray
application of primers and topcoats that
contain inorganic HAP. Based on the
results of the 2011 ICR, the EPA has
determined that the vast majority of
spray-applied specialty coatings are
currently applied in spray booths. It is
likely that these specialty coatings are
applied in the same spray booths as
primers and topcoats, or at least in spray
booths that are very similar to those
used for primer and topcoat operations.
Therefore, the same inorganic HAP
emission limitations that are applied to
primer and topcoat operations should
also be applicable to specialty coating
operations, and the EPA is proposing to
extend these limitations to specialty
coating operations. The EPA has not
identified any control options more
stringent than the use of spray booths
with high-efficiency filters to control
inorganic HAP emissions from sprayapplied coating operations.
In summary, the EPA is proposing to
add a requirement to the Aerospace
NESHAP that Aerospace Manufacturing
and Rework Facilities comply with
organic HAP or VOC content limits for
specialty coatings that are equal to the
VOC content limits specified in the
Aerospace CTG. The EPA is also
proposing that specialty coating
application operations be subject to the
same application equipment
requirements in 40 CFR 63.745(f), and
the standards for inorganic HAP
emissions in 40 CFR 63.745(g) that
apply to primer and topcoat application
operations. We request comment on our
analysis and supporting info on any
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other practices that may be used to limit
emissions from specialty coatings.
The EPA believes that the proposed
HAP and VOC content limits for
specialty coatings are achievable
because they are based on the VOC
content limits in the Aerospace CTG,
which have been adopted in many state
and local VOC rules. In the
development of these proposed
amendments, the EPA made repeated
efforts to reach out to and solicit input
from aerospace manufacturers on the
coating performance and reformulation
challenges, if any, presented by
complying with specialty coating limits
based on the current CTG. However, the
information presented so far has been
only anecdotal, and not for the full
range of specialty coating categories in
the CTG.
Therefore, the EPA is specifically
soliciting comment and additional data
on any changes needed to the
definitions of specialty coating
categories and the proposed organic
HAP and VOC limits. The EPA will
consider comments on changes to the
definitions of specialty coating
categories that may be needed to clarify
the scope of each of the individual
specialized coating categories, based on
industry experience, including
complying with those categories in rules
derived from the Aerospace CTG. The
EPA will consider data and information
on specific cases (not just general
examples) of specialty coatings that
could not meet the current definitions of
the specialty coating categories or the
proposed organic HAP or VOC content
limits for those categories. Please
provide with your comments
information on the following: The
annual volume of the coating used, the
container size, the container type, the
military specification or FAA AD that
applies, the specialty category that
applies, documentation of the organic
HAP or VOC content of the coating and
suggested changes to category
definitions (if applicable and feasible)
that would include the coating in a
more appropriate category with a higher
HAP or VOC limit. The EPA will
consider any submitted data that
supports a comment that a specific
coating cannot meet the proposed
organic HAP or VOC content limit for a
particular specialty coating category.
The estimated costs, emission
reductions, other (non-air)
environmental impacts and energy
impacts associated with the proposed
regulation of specialty coatings are
presented in section V of this preamble.
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2. Electronic Reporting Requirements
In this proposal, the EPA is describing
a process to increase the ease and
efficiency of performance test data
submittal while improving data
accessibility. Specifically, the EPA is
proposing that owners and operators of
Aerospace Manufacturing and Rework
Facilities submit electronic copies of
required performance test and
performance evaluation reports by
direct computer-to-computer electronic
transfer using EPA-provided software.
The direct computer-to-computer
electronic transfer is accomplished
through the EPA’s Central Data
Exchange (CDX) using the Compliance
and Emissions Data Reporting Interface
(CEDRI). The CDX is the EPA’s portal
for submittal of electronic data. The
EPA-provided software is called the
Electronic Reporting Tool (ERT), which
is used to generate electronic reports of
performance tests and evaluations. The
ERT generates an electronic report
package which will be submitted using
the CEDRI. The submitted report
package will be stored in the CDX
archive (the official copy of record) and
the EPA’s public database called
WebFIRE. The WebFIRE database was
constructed to store performance test
data for use in developing emissions
factors. All stakeholders would have
access to all reports and data in
WebFIRE and accessing these reports
and data will be very straightforward
and easy (see the WebFIRE Report
Search and Retrieval link at https://
cfpub.epa.gov/webfire/index.cfm?
action=fire.searchERTSubmission). A
description of the WebFIRE database is
available at https://cfpub.epa.gov/
oarweb/index.cfm?action=fire.main. A
description of the ERT and instructions
for using ERT can be found at https://
www.epa.gov/ttn/chief/ert/ert_tool.html.
CEDRI can be accessed through the CDX
Web site (www.epa.gov/cdx).
The proposal to submit performance
test data electronically to the EPA
would apply only to those performance
tests conducted using test methods that
will be supported by the ERT. The ERT
contains a specific electronic data entry
form for most of the commonly used
EPA reference methods. A listing of the
pollutants and test methods supported
by the ERT is available at https://
www.epa.gov/ttn/chief/ert/.
We believe that industry would benefit
from this proposed approach to
electronic data submittal. Specifically,
by using this approach, industry would
save time in the performance test
submittal process. Additionally, the
standardized format that the ERT uses
allows sources to create a more
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complete test report resulting in less
potential failure to include all data
elements required to be submitted. Also
through this proposal, industry may
only need to submit a report once to
meet the requirements of the applicable
subpart because stakeholders can
readily access these reports from the
WebFIRE database. This also would
benefit industry by cutting back on
recordkeeping costs as the performance
test reports that are submitted to the
EPA using CEDRI are no longer required
to be retained in hard copy, thereby
reducing staff time needed to coordinate
these records. Another benefit to
industry is that, because the EPA would
already have performance test data in
hand, industry would be subject to
fewer or less substantial data collection
requests from EPA in conjunction with
required future residual risk
assessments or technology reviews. This
would result in a decrease in industry
staff time needed to respond to data
collection requests.
State, local and tribal air pollution
control agencies (S/L/Ts) may also
benefit from having electronic versions
of the reports they are now receiving.
For example, S/L/Ts may be able to
conduct a more streamlined and
accurate review of electronic data
submitted to them. The ERT would
allow for an electronic review process,
rather than a manual data assessment,
which will make review and evaluation
of the source provided data and
calculations easier and more efficient. In
addition, the public will benefit from
electronic reporting of emissions data
because the electronic data will be
easier for the public to access. How the
air emissions data are collected,
accessed and reviewed will be more
transparent for all stakeholders.
Further, the EPA must have
performance test data to conduct
effective reviews of CAA sections 112
and 129 standards, as well as for many
other purposes including compliance
determinations, emissions factor
development and annual emissions rate
determinations. In conducting these
required reviews, the EPA has found it
ineffective and time consuming, not
only for the EPA, but also for regulatory
agencies and source owners and
operators, to locate, collect and submit
performance test data because of varied
locations for data storage and varied
data storage methods. In recent years,
though, stack testing firms have
typically collected performance test data
in electronic format, making it possible
to move to an electronic data submittal
system that would increase the ease and
efficiency of data submittal and improve
data accessibility.
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One major advantage of the proposed
submittal of performance test data
through the ERT is a standardized
method to compile and store much of
the documentation required to be
reported by this rule. Another advantage
is that the ERT clearly states what
testing information would be required.
Another important proposed benefit of
submitting these data to the EPA at the
time the source test is conducted is that
it should substantially reduce the effort
involved in data collection activities in
the future. When the EPA has
performance test data in hand, the EPA
will be able to conduct fewer or less
substantial data collection requests in
conjunction with future required
residual risk assessments or technology
reviews. This would result in a reduced
burden on both affected facilities (in
terms of reduced staff time to respond
to data collection requests) and the EPA
(in terms of preparing and distributing
data collection requests and assessing
the results).
Finally, another benefit of the
proposed data submittal to WebFIRE
electronically is that these data would
greatly improve the overall quality of
existing and new emissions factors by
supplementing the pool of emissions
test data for establishing emissions
factors and by ensuring that the factors
are more representative of current
industry operational procedures. A
common complaint heard from industry
and regulators is that emissions factors
are outdated or not representative of a
particular source category. With timely
receipt and incorporation of data from
most performance tests, the EPA would
be able to ensure that emissions factors,
when updated, represent the most
current range of operational practices.
In summary, in addition to supporting
regulation development, control strategy
development and other air pollution
control activities, having an electronic
database populated with performance
test data would save industry, state,
local, tribal agencies and the EPA
significant time, money and effort while
also improving the quality of emissions
inventories and, as a result, air quality
regulations.
3. Startup, Shutdown and Malfunction
Requirements
In its 2008 decision in Sierra Club v.
EPA, 551 F.3d 1019 (D.C. Cir. 2008),
cert. denied, 130 S. Ct. 1735 (U.S. 2010),
the United States Court of Appeals for
the District of Columbia Circuit vacated
portions of two provisions in the EPA’s
CAA section 112 regulations governing
the emissions of HAP during periods of
SSM. Specifically, the court vacated the
SSM exemption contained in 40 CFR
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63.6(f)(1) and (h)(1), holding that under
section 302(k) of the CAA, emissions
standards or limitations must be
continuous in nature and that the SSM
exemption violates the CAA’s
requirement that some section 112
standards apply continuously.
We are proposing the elimination of
the SSM exemption in this rule.
Consistent with Sierra Club v. EPA, we
are proposing changes so that standards
in this rule would apply at all times. We
are also proposing several revisions to
Table 1 to subpart GG of Part 63 (the
General Provisions Applicability Table,
hereafter referred to as the ‘‘General
Provisions table’’) as explained in more
detail below. For example, we are
proposing to eliminate the incorporation
of the General Provisions’ requirement
that the source develop an SSM plan.
We also are proposing to eliminate and
revise certain recordkeeping and
reporting requirements related to the
SSM exemption as further described
below.
The EPA has attempted to ensure that
the provisions we are proposing to
eliminate are inappropriate,
unnecessary or redundant in the
absence of the SSM exemption. We are
specifically seeking comment on
whether we have successfully done so.
In proposing the standards in this
rule, the EPA has taken into account
startup and shutdown periods and, for
the reasons explained below, has not
proposed alternate standards for those
periods.
Periods of startup, normal operations
and shutdown are all predictable and
routine aspects of a source’s operations.
Malfunctions, in contrast, are neither
predictable nor routine. Instead they
are, by definition sudden, infrequent
and not reasonably preventable failures
of emissions control, process or
monitoring equipment. The EPA
interprets CAA section 112 as not
requiring emissions that occur during
periods of malfunction to be factored
into development of CAA section 112
standards. Under section 112, emissions
standards for new sources must be no
less stringent than the level ‘‘achieved’’
by the best controlled similar source
and, for existing sources, generally must
be no less stringent than the average
emission limitation ‘‘achieved’’ by the
best performing 12 percent of sources in
the category. There is nothing in section
112 that directs the agency to consider
malfunctions in determining the level
‘‘achieved’’ by the best performing
sources when setting emission
standards. As the D.C. Circuit has
recognized, the phrase ‘‘average
emissions limitation achieved by the
best performing 12 percent of’’ sources
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‘‘says nothing about how the
performance of the best units is to be
calculated.’’ Nat’l Ass’n of Clean Water
Agencies v. EPA, 734 F.3d 1115, 1141
(D.C. Cir. 2013). While the EPA
accounts for variability in setting
emissions standards, nothing in CAA
section 112 requires the agency to
consider malfunctions as part of that
analysis. A malfunction should not be
treated in the same manner as the type
of variation in performance that occurs
during routine operations of a source. A
malfunction is a failure of the source to
perform in a ‘‘normal or usual manner’’
and no statutory language compels the
EPA to consider such events in setting
CAA section 112 standards.
Further, accounting for malfunctions
in setting emission standards would be
difficult, if not impossible, given the
myriad different types of malfunctions
that can occur across all sources in the
category and given the difficulties
associated with predicting or accounting
for the frequency, degree and duration
of various malfunctions that might
occur. As a result, the performance of
units that are malfunctioning is not
‘‘reasonably’’ foreseeable. See, e.g.
Sierra Club v. EPA, 167 F.3d 658, 662
(D.C. Cir. 1999) (‘‘The EPA typically has
wide latitude in determining the extent
of data-gathering necessary to solve a
problem. We generally defer to an
agency’s decision to proceed on the
basis of imperfect scientific information,
rather than to ‘invest the resources to
conduct the perfect study.’ ’’) See also,
Weyerhaeuser v. Costle, 590 F.2d 1011,
1058 (D.C. Cir. 1978) (‘‘In the nature of
things, no general limit, individual
permit, or even any upset provision can
anticipate all upset situations. After a
certain point, the transgression of
regulatory limits caused by
‘uncontrollable acts of third parties,’
such as strikes, sabotage, operator
intoxication or insanity and a variety of
other eventualities, must be a matter for
the administrative exercise of case-bycase enforcement discretion, not for
specification in advance by
regulation.’’). In addition, emissions
during a malfunction event can be
significantly higher than emissions at
any other time of source operation. For
example, if an air pollution control
device with 99-percent removal goes offline as a result of a malfunction (as
might happen if, for example, the bags
in a baghouse catch fire) and the
emission unit is a steady-state type unit
that would take days to shut down, the
source would go from 99-percent
control to zero control until the control
device was repaired. The source’s
emissions during the malfunction
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would be 100 times higher than during
normal operations and the emissions
over a 4-day malfunction period would
exceed the annual emissions of the
source during normal operations. As
this example illustrates, accounting for
malfunctions could lead to standards
that are not reflective of (and
significantly less stringent than) levels
that are achieved by a well-performing
non-malfunctioning source. It is
reasonable to interpret CAA section 112
to avoid such a result. The EPA’s
approach to malfunctions is consistent
with CAA section 112 and is a
reasonable interpretation of the statute.
In the event that a source fails to
comply with the applicable CAA section
112 standards as a result of a
malfunction event, the EPA would
determine an appropriate response
based on, among other things, the good
faith efforts of the source to minimize
emissions during malfunction periods,
including preventative and corrective
actions, as well as root cause analyses
to ascertain and rectify excess
emissions. The EPA would also
consider whether the source’s failure to
comply with the CAA section 112
standard was, in fact, sudden,
infrequent, not reasonably preventable
and was not instead caused in part by
poor maintenance or careless operation.
If the EPA determines that an
enforcement action against a source for
violation of an emission standard is
warranted, the source can raise any and
all defenses in that enforcement action
and the federal district court will
determine what, if any, relief is
appropriate. The same is true for citizen
enforcement actions. Similarly, the
presiding officer in an administrative
proceeding can consider any defense
raised and determine whether
administrative penalties are appropriate.
In summary, the EPA interpretation of
the CAA and, in particular, CAA section
112 is reasonable and encourages
practices that will avoid malfunctions.
Administrative and judicial procedures
for addressing exceedances of the
standards fully recognize that violations
may occur despite good faith efforts to
comply and can accommodate those
situations.
In several prior CAA section 112
rules, the EPA had included an
affirmative defense to civil penalties for
violations caused by malfunctions in an
effort to create a system that
incorporates some flexibility,
recognizing that there is a tension,
inherent in many types of air regulation,
to ensure adequate compliance while
simultaneously recognizing that despite
the most diligent of efforts, emission
standards may be violated under
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circumstances entirely beyond the
control of the source. Although the EPA
recognized that its case-by-case
enforcement discretion provides
sufficient flexibility in these
circumstances, it included the
affirmative defense to provide a more
formalized approach and more
regulatory clarity. See Weyerhaeuser Co.
v. Costle, 590 F.2d 1011, 1057–58 (D.C.
Cir. 1978) (holding that an informal
case-by-case enforcement discretion
approach is adequate); but see Marathon
Oil Co. v. EPA, 564 F.2d 1253, 1272–73
(9th Cir. 1977) (requiring a more
formalized approach to consideration of
‘‘upsets beyond the control of the permit
holder’’). Under the EPA’s regulatory
affirmative defense provisions, if a
source could demonstrate in a judicial
or administrative proceeding that it had
met the requirements of the affirmative
defense in the regulation, civil penalties
would not be assessed. Recently, the
United States Court of Appeals for the
District of Columbia Circuit vacated an
affirmative defense in one of the EPA’s
CAA section 112 regulations. NRDC v.
EPA, 749 F.3d 1055 (D.C. Cir., 2014)
(vacating affirmative defense provisions
in CAA section 112 rule establishing
emission standards for Portland cement
kilns). The court found that the EPA
lacked authority to establish an
affirmative defense for private civil suits
and held that under the CAA, the
authority to determine civil penalty
amounts in such cases lies exclusively
with the courts, not the EPA.
Specifically, the court found: ‘‘As the
language of the statute makes clear, the
courts determine, on a case-by-case
basis, whether civil penalties are
‘appropriate.’’’ See NRDC, 2014 U.S.
App. LEXIS 7281 at *21 (‘‘[U]nder this
statute, deciding whether penalties are
‘appropriate’ in a given private civil suit
is a job for the courts, not EPA.’’).36 In
light of NRDC, the EPA is not including
a regulatory affirmative defense
provision in the proposed rule. As
explained above, if a source is unable to
comply with emissions standards as a
result of a malfunction, the EPA may
use its case-by-case enforcement
discretion to provide flexibility, as
appropriate. Further, as the United
States Court of Appeals for the District
of Columbia Circuit recognized, in an
EPA or citizen enforcement action, the
court has the discretion to consider any
defense raised and determine whether
penalties are appropriate. Cf. NRDC,
36 The court’s reasoning in NRDC v. EPA focuses
on civil judicial actions. The Court noted that
‘‘EPA’s ability to determine whether penalties
should be assessed for Clean Air Act violations
extends only to administrative penalties, not to civil
penalties imposed by a court.’’ Id.
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(arguments that violation were caused
by unavoidable technology failure can
be made to the courts in future civil
cases when the issue arises). The same
is true for the presiding officer in EPA
administrative enforcement actions.37
a. 40 CFR 63.743(e) General Duty
We are proposing to revise the entry
in the General Provisions table for 40
CFR 63.6(e)(1)(i) by changing the ‘‘yes’’
in column 2 to a ‘‘no.’’ Section
63.6(e)(1)(i) describes the general duty
to minimize emissions. Some of the
language in that section is no longer
necessary or appropriate in light of the
elimination of the SSM exemption. We
are proposing instead to add general
duty regulatory text at 40 CFR 63.743(e)
that reflects the general duty to
minimize emissions while eliminating
the reference to periods covered by an
SSM exemption. The current language
in 40 CFR 63.6(e)(1)(i) characterizes
what the general duty entails during
periods of SSM. With the elimination of
the SSM exemption, there is no need to
differentiate between normal operations,
startup and shutdown and malfunction
events in describing the general duty.
Therefore the language the EPA is
proposing for 40 CFR 63.743(e) does not
include that language from 40 CFR
63.6(e)(1).
We are also proposing to revise the
General Provisions table entry for 40
CFR 63.6(e)(1)(ii) by changing the ‘‘yes’’
in column 2 to a ‘‘no.’’ Section
63.6(e)(1)(ii) imposes requirements that
are not necessary with the elimination
of the SSM exemption or are redundant
with the general duty requirement being
added at 40 CFR 63.743(e).
b. SSM Plan
We are proposing to revise the
General Provisions table entry for 40
CFR 63.6(e)(3) by changing the ‘‘yes’’ in
column 2 to a ‘‘no.’’ Generally, these
paragraphs require development of an
SSM plan and specify SSM
recordkeeping and reporting
requirements related to the SSM plan.
As noted, the EPA is proposing to
remove the SSM exemptions. Therefore,
affected units will be subject to an
37 Although the NRDC v. EPA case does not
address the EPA’s authority to establish an
affirmative defense to penalties that is available in
administrative enforcement actions, the EPA is not
including such an affirmative defense in the
proposed rule. As explained above, such an
affirmative defense is not necessary. Moreover,
assessment of penalties for violations caused by
malfunctions in administrative proceedings and
judicial proceedings should be consistent. CF. CAA
section 113(e) (requiring both the Administrator
and the court to take specified criteria into account
when assessing penalties).
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emission standard during such events.
The applicability of a standard during
such events will ensure that sources
have ample incentive to plan for and
achieve compliance and, thus, the SSM
plan requirements are no longer
necessary.
tkelley on DSK3SPTVN1PROD with PROPOSALS2
c. Compliance With Standards
We are proposing to revise the
General Provisions table entry for 40
CFR 63.6(f)(1) by changing the ‘‘yes’’ in
column 2 to a ‘‘no.’’ The current
language of 40 CFR 63.6(f)(1) exempts
sources from non-opacity standards
during periods of SSM. As discussed
above, the court in Sierra Club v. EPA
vacated the exemptions contained in
this provision and held that the CAA
requires that some CAA section 112
standards apply continuously.
Consistent with Sierra Club, the EPA is
proposing to revise some standards in
this rule to apply at all times.
d. 40 CFR 63.749(j) Performance Testing
We are proposing to revise the
General Provisions table entry for 40
CFR 63.7(e)(1) by changing the ‘‘yes’’ in
column 2 to a ‘‘no.’’ Section 63.7(e)(1)
describes performance testing
requirements. The EPA is instead
proposing to add a performance testing
requirement at 40 CFR 63.749(j). The
performance testing requirements we
are proposing to add differ from the
General Provisions performance testing
provisions in several respects. The
regulatory text does not include the
language in 40 CFR 63.7(e)(1) that
restated the SSM exemption and
language that precluded startup and
shutdown periods from being
considered ‘‘representative’’ for
purposes of performance testing. The
proposed performance testing
provisions will specify that performance
testing of controls must be conducted
during representative operating
conditions of the applicable source, and
may not take place during startup,
shutdown or malfunction of the
applicable controlled surface coating
operations, controlled chemical milling
maskant application operations or
controlled chemical depainting
operations. As in 40 CFR 63.7(e)(1),
performance tests conducted under this
subpart should not be conducted during
malfunctions because conditions during
malfunctions are often not
representative of normal operating
conditions. The EPA is proposing to add
language that requires the owner or
operator to record the process
information that is necessary to
document operating conditions during
the test and include in such record an
explanation to support that such
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conditions represent normal operation.
Section 63.7(e) requires that the owner
or operator make available to the
Administrator such records ‘‘as may be
necessary to determine the condition of
the performance test’’ available to the
Administrator upon request, but does
not specifically require the information
to be recorded. The regulatory text the
EPA is proposing to add to this
provision builds on that requirement
and makes explicit the requirement to
record the information.
e. Monitoring
We are proposing to revise the
General Provisions table entry for 40
CFR 63.8(c)(1)(i) and (iii) by changing
the ‘‘yes’’ in column 2 to a ‘‘no.’’ The
cross-references to the general duty and
SSM plan requirements in those
subparagraphs are not necessary in light
of other requirements of 40 CFR 63.8
that require good air pollution control
practices (40 CFR 63.8(c)(1)) and that set
out the requirements of a quality control
program for monitoring equipment (40
CFR 63.8(d)).
f. 40 CFR 63.752(a) Recordkeeping
We are proposing to revise the
General Provisions table entry for 40
CFR 63.10(b)(2)(i) by changing the ‘‘yes’’
in column 2 to a ‘‘no.’’ Section
63.10(b)(2)(i) describes the
recordkeeping requirements during
startup and shutdown. These recording
provisions are no longer necessary
because the EPA is proposing that
recordkeeping and reporting applicable
to normal operations will apply to
startup and shutdown. In the absence of
special provisions applicable to startup
and shutdown, such as a startup and
shutdown plan, there is no reason to
retain additional recordkeeping for
startup and shutdown periods.
We are proposing to revise the
General Provisions table entry for 40
CFR 63.10(b)(2)(ii) by changing the
‘‘yes’’ in column 2 to a ‘‘no.’’ Section
63.10(b)(2)(ii) describes the
recordkeeping requirements during a
malfunction. The EPA is proposing to
add such requirements to 40 CFR
63.752(a). The regulatory text we are
proposing to add differs from the
General Provisions it is replacing in that
the General Provisions requires the
creation and retention of a record of the
occurrence and duration of each
malfunction of process, air pollution
control and monitoring equipment. The
EPA is proposing that this requirement
apply to any failure to meet an
applicable standard and is requiring that
the source record the date, time and
duration of the failure rather than the
‘‘occurrence.’’ The EPA is also
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8425
proposing to add to 40 CFR 63.752(a) a
requirement that sources keep records
that include a list of the affected source
or equipment and actions taken to
minimize emissions, an estimate of the
quantity of each regulated pollutant
emitted over the standard for which the
source failed to meet the standard and
a description of the method used to
estimate the emissions. Examples of
such methods would include mass
balance calculations, measurements
when available or engineering judgment
based on known process parameters
(e.g., coating HAP content and
application rate or control device
efficiencies). The EPA is proposing to
require that sources keep records of this
information to ensure that there is
adequate information to allow the EPA
to determine the severity of any failure
to meet a standard and to provide data
that may document how the source met
the general duty to minimize emissions
when the source has failed to meet an
applicable standard.
We are proposing to revise the
General Provisions table entry for 40
CFR 63.10(b)(2)(iv) by changing the
‘‘yes’’ in column 2 to a ‘‘no.’’ When
applicable, the provision requires
sources to record actions taken during
SSM events when actions were
inconsistent with their SSM plan. The
requirement is no longer appropriate
because SSM plans will no longer be
required. The requirement previously
applicable under 40 CFR
63.10(b)(2)(iv)(B) to record actions to
minimize emissions and record
corrective actions is now applicable by
reference to 40 CFR 63.752(a).
We are proposing to revise the
General Provisions table entry for 40
CFR 63.10(b)(2)(v) by changing the
‘‘yes’’ in column 2 to a ‘‘no.’’ When
applicable, the provision requires
sources to record actions taken during
SSM events to show that actions taken
were consistent with their SSM plan.
The requirement is no longer
appropriate because SSM plans will no
longer be required.
g. 40 CFR 63.753 Reporting
We are proposing to revise the
General Provisions table entry for 40
CFR 63.10(d)(5) by changing the ‘‘yes’’
in column 2 to a ‘‘no.’’ Section
63.10(d)(5) describes the reporting
requirements for startups, shutdowns
and malfunctions. To replace the
General Provisions reporting
requirement, the EPA is proposing to
add reporting requirements to 40 CFR
63.753(a). The replacement language
added to 40 CFR 63.753(a) differs from
the General Provisions requirement in
that it eliminates periodic SSM reports
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as a stand-alone report. We are
proposing language that requires
sources that fail to meet an applicable
standard at any time to report the
information concerning such events in
the semi-annual reporting period
already required under this rule. We are
proposing that the report must contain
the number, date, time, duration and the
cause of such events (including
unknown cause, if applicable), a list of
the affected source or equipment, an
estimate of the quantity of each
regulated pollutant emitted over any
emission limit and a description of the
method used to estimate the emissions.
Examples of such methods would
include mass balance calculations,
measurements when available or
engineering judgment based on known
process parameters (e.g., coating HAP
content and application rates and
control device efficiencies). The EPA is
proposing this requirement to ensure
that there is adequate information to
determine compliance, to allow the EPA
to determine the severity of the failure
to meet an applicable standard and to
provide data that may document how
the source met the general duty to
minimize emissions during a failure to
meet an applicable standard.
We would no longer require owners
or operators to determine whether
actions taken to correct a malfunction
are consistent with an SSM plan,
because plans would no longer be
required. The proposed amendments
would, therefore, eliminate the cross
reference to 40 CFR 63.10(d)(5)(i) that
contains the description of the
previously required SSM report format
and submittal schedule from this
section. These specifications would be
no longer necessary because the events
would be reported in otherwise required
reports with similar format and
submittal requirements.
As discussed above, we are proposing
to revise the General Provisions table
entry for 40 CFR 63.10(d)(5), by
changing the ‘‘yes’’ in column 2 to a
‘‘no.’’ Section 63.10(d)(5)(ii) describes
an immediate report for startups,
shutdown and malfunctions when a
source failed to meet an applicable
standard, but did not follow the SSM
plan. We will no longer require owners
and operators to report when actions
taken during a startup, shutdown or
malfunction were not consistent with an
SSM plan, because plans would no
longer be required to allow the EPA to
determine the severity of the failure to
meet an applicable standard and to
provide data that may document how
the source met the general duty to
minimize emissions during a failure to
meet an applicable standard.
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spills, apply these coatings using one or
more of the specified application
techniques and comply with inorganic
The EPA is also proposing the
HAP emission requirements.
following technical corrections:
This change is being proposed to
• Revising 40 CFR 63.743(a)(2) to
reduce unnecessary recordkeeping and
match the section title in 40 CFR 63.5.
avoid the need for owners or operators
• Revising 40 CFR 63.743(a)(8) to
to perform tests to measure VOC and
correct the reference to paragraph
HAP content and to perform certain
63.6(i)(12)(iii)(B) by changing the ‘‘(1)’’
calculations that can be done by the
to an ‘‘(i).’’
coating manufacturer based on coating
• Revising 40 CFR 63.744(a) to correct
formulation data. When the Aerospace
and clarify the format of the reference to NESHAP was originally promulgated,
40 CFR 63.744(a)(1) through (4).
the original compliance demonstration
• Correct the ordering of 40 CFR
and recordkeeping requirements were
63.744(a)(3) and (4); currently paragraph needed because the product data sheets
(a)(4) is printed before (a)(3).
provided by coating manufacturers did
• Correcting the paragraph numbering not routinely provide VOC content in
for 40 CFR 63.746(b)(4)(ii)(C) by
grams per liter (less water and exempt
changing paragraph (C) from a lower
solvents) or HAP content in grams per
case to upper case ‘‘C.’’
liter (less water). As a result, it was
• Correcting the numbering of the
necessary for the facilities to calculate
tables in 40 CFR 63.745 to account for
the VOC or HAP content in this format
the proposed addition of Table 1 to that to demonstrate compliance.
section to include specialty coating
Since promulgation of the Aerospace
limits.
NESHAP, coating manufacturers now
• Revising 40 CFR 63.749(d)(4) to
commonly provide VOC content of the
correct the references to 40 CFR
coatings, in grams per liter (less water
63.749(d)(4)(i) through (d)(4)(iv) and (e). and exempt solvents) on the product
• Revising 40 CFR 63.750(g)(6)(i) to
data sheets, based on coating
remove the letters ‘‘VR/FD’’ that were
formulation. Therefore, the coating
inadvertently included.
manufacturer’s documentation can be
used to demonstrate compliance, when
5. Amendments To Simplify
available, in place of the compliance
Recordkeeping and Reporting for
demonstrations based on VOC
Compliant Coatings
measurements and compliance
The EPA is proposing to revise 40
calculations.
CFR 63.750 to include alternative
We are proposing that this alternative
compliance demonstration provisions
apply to all coatings subject to the
for all coatings subject to the Aerospace Aerospace NESHAP, including specialty
NESHAP (primers, topcoats, specialty
coatings, topcoats, primers and
coatings and chemical milling
chemical milling maskants. Due to the
maskants). If the manufacturer’s
existence of the Aerospace NESHAP for
supplied formulation data or calculation nearly 20 years and the prevalence of
of HAP and VOC content indicate that
state and regional VOC regulations for
the coating meets the organic HAP and
many types of coatings, coating
VOC content emission limits for its
manufacturers have come to recognize
coating type, as specified in 40 CFR
the value of providing documentation of
63.745(c) and 63.747(c), then the owner HAP and VOC content to their
or operator would not be required to
customers to facilitate compliance
demonstrate compliance for these
demonstrations with state and federal
coatings using the test method and
regulations. For all coatings subject to
calculations specified in 40 CFR
the Aerospace NESHAP, the EPA has
63.750(c), (e), (k) and (m) or to keep the
determined that onsite purchase records
associated records and submit the
and the manufacturer’s supplied data
associated reports associated with these sheets for the coatings will provide
methods and calculations. Instead, the
sufficient information to establish
owner or operator would be able to rely
compliance with the content limit
on the manufacturers’ formulation data
standards in the Aerospace NESHAP.
If a facility elects to comply with the
and calculation of the HAP or VOC
averaging provisions in 40 CFR
content to demonstrate compliance.
63.743(d), the facility is also required to
However, the owner or operator would
comply with all related averaging
still be required to maintain purchase
provisions in the Aerospace NESHAP
records and manufacturer’s supplied
data sheets for these compliant coatings. for all coatings included in averaging
(e.g., compliance determination
Owners or operators of facilities using
provisions in 40 CFR 63.749(d) and (h);
these coatings would also still be
procedures and methods in 40 CFR
required to handle and transfer these
63.750(d), (f), (l) and (n); recordkeeping
coatings in a manner that minimizes
4. Technical Amendments to the
Aerospace NESHAP
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provisions in 40 CFR 63.752(c) and (f);
and reporting provisions in 63.753(c)
and (e)). Note that, in complying with
the current averaging provisions,
facilities may already use
manufacturers’ data for coatings to
determine the organic HAP and VOC
weight fraction of coatings to perform
the calculations in 40 CFR 63.750(d), (f),
(l) and (n).
F. What compliance dates are we
proposing?
tkelley on DSK3SPTVN1PROD with PROPOSALS2
The EPA is proposing that all of the
amendments being proposed in this
action would be effective on the date 60
days after these proposed amendments
are final, with one exception. The one
exception is that existing specialty
coating affected sources (i.e., existing on
the date these changes are final) would
have 1 year after the date this rule is
final to comply with the standards for
specialty coatings proposed in 40 CFR
63.745(c)(5) and (6) (HAP and VOC
limits for specified coatings) and the
provisions in 40 CFR 63.745(f) (coating
application equipment) and 40 CFR
63.745(g) (control of inorganic HAP
emissions). The EPA is proposing this
compliance schedule so that existing
sources would have time to develop the
recordkeeping and reporting systems
needed to comply with the requirements
for specialty coatings. Facilities may
also need this time to identify
alternative coatings for those that are
not currently compliant with the HAP
or VOC content limits and to take any
steps needed to upgrade specialty
coating operations to comply with the
application equipment requirements in
40 CFR 63.745(f) and the inorganic HAP
emissions requirements in 40 CFR
63.745(g).
The tasks necessary for existing
facilities to comply with the other
proposed amendments require no time
or resources. Therefore, EPA believes
that existing facilities will be able to
comply with the other proposed
amendments, including those related to
SSM periods, as soon as the final rule
is effective, which will be the date 60
days after publication of the final rule.
Therefore, the EPA is specifically
soliciting comment and additional data
on the burden of complying with the
other proposed amendments.
V. Summary of Cost, Environmental
and Economic Impacts
A. What are the affected sources?
The EPA estimates, based on the
responses to the 2011 ICR, that there are
144 major source facilities that are
engaged in aerospace manufacturing
and rework surface coating operations.
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The EPA estimates that 109 facilities
likely would be affected by the
proposed limits for specialty coatings
and the requirements to use highefficiency application equipment for
specialty coatings, also based on the
responses to the 2011 ICR.
B. What are the air quality impacts?
The EPA estimates that annual HAP
emissions from specialty coatings are
about 360 tpy; inorganic HAP emissions
are about 5 tpy and the remainder are
organic HAP. The estimated emission
reductions are 58 tons of HAP, which
would be achieved from the proposed
regulation of specialty coatings. The
EPA estimated that these emission
reductions would result from the
proposed requirements to use highefficiency application equipment and
also from the application of the HAP
content limits to specialty coatings.
C. What are the cost impacts?
The EPA estimates that the annual
cost impacts would be about $590,000
per year. The cost impacts would be
attributed to monitoring and
recordkeeping costs for complying with
the specialty coating HAP content
limits. The cost per facility was
estimated based on the number of
specialty coatings used at each facility,
as reported in the 2011 ICR. The costs
are based on an assumption of 1 hour
of technical labor for annual
recordkeeping and reporting for each
specialty coating used by a facility, plus
additional management and clerical
hours representing a fraction of the
technical labor hours.
The EPA does not have sufficient data
from the 2011 ICR to estimate the total
cost impacts for specialty coatings
having to comply with the proposed
high-efficiency application equipment
requirement. Because high-efficiency
application equipment generates less
coating overspray than conventional
equipment, the costs of upgrading to
new equipment can be offset by cost
savings from reduced coating
consumption and reduced spray booth
filter maintenance. For these reasons,
many facilities are likely to have already
switched to high-efficiency application
methods for specialty coating
operations, as they are already required
to for primer and topcoat application
operations. For example, the average
volume of specialty coatings used per
facility is 3,000 gallons per year, based
on the 2011 ICR data. The estimated
purchase cost for a professional quality
HVLP spray gun is $700 for the gun and
hoses. If the average facility had to
purchase three new spray guns, and the
facility was spending an average of $30
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per gallon of spray applied coating, the
facility would need to see a decrease in
coating consumption of only 70 gallons
per year (about a 3-percent reduction) to
recover the initial cost of those three
spray guns in 1 year.
The EPA expects some additional
potential cost savings from the proposal
to include an alternative compliance
demonstration provision in 40 CFR
63.750(c), (e), (k) and (m). However, we
do not have sufficient data to estimate
the cost savings associated with the
proposed alternative compliance
demonstration. However, the estimated
cost to perform an analysis of VOC
content according to EPA Method 24,
based on published vendor data, is
about $575 per sample. Because the
proposed alternative compliance
demonstration would allow facilities to
use coating manufacturers’
documentation of VOC content based on
coating composition, the cost of these
coating analyses using EPA Method 24
would be avoided.
The EPA’s cost analyses are
documented in the memorandum,
Methodology for Estimating Control
Costs for Specialty Coating Operations
in the Aerospace Source Category,
January 2014, in the docket for this
rulemaking.
EPA is specifically soliciting
comment and additional data on the
cost impacts associated with using
coatings that are compliant with the
proposed limits for specialty coatings.
D. What are the economic impacts?
Economic impact analyses focus on
changes in market prices and output
levels. If changes in market prices and
output levels in the primary markets are
significant enough, impacts on other
markets are also examined. Both the
magnitude of costs needed to comply
with the rule and the distribution of
these costs among affected facilities can
have a role in determining how the
market will change in response to a rule.
This rule applies to the surface
coating and related operations at
facilities that are major sources and are
engaged, either in part or in whole, in
the manufacture or rework of
commercial, civil or military aerospace
vehicles or components. The proposed
rule would add recordkeeping and
reporting provisions for specialty
coating operations, but would not
change the compliance costs for
operations already being regulated by
the existing emission standards.
Therefore, the annual costs were
calculated for only the 109 Aerospace
Manufacturing and Rework Facilities
that reported having specialty coating
operations.
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The estimated annual costs for this
proposed rule are less than $1 million
in the first year and in succeeding years
(less than $850,000 in the first year and
less than $600,000 in succeeding years).
These costs are estimated for the 109
facilities that, based on information
reported by facilities, appear to have
specialty coating operations. Thus, the
average cost per facility is less than
$10,000 per year. These costs are small
compared to sales for the companies in
aerospace manufacturing and
reworking. For example, in 2012 the
average annual value of shipments (a
rough estimate of sales) for firms in the
category of ‘‘other aircraft parts and
auxiliary equipment manufacturing’’
was almost $50 million (Source: U.S.
Census Bureau, 2012 Economic Census
for NAICS 336413 for 2012). In this case
the cost-to-sales estimate would be
approximately 0.02 percent of sales for
each firm. Costs this small would not
have significant market impacts,
whether they were absorbed by the firm
or passed on as price increases.
The EPA does not know of any firms
that are small entities and using
specialty coatings that are potentially
subject to this proposed rule. Because
no small firms face control costs, there
is no significant impact on small
entities. Therefore, we do not expect
these proposed amendments to have a
significant impact on a substantial
number of small entities.
tkelley on DSK3SPTVN1PROD with PROPOSALS2
E. What are the benefits?
We anticipate this rulemaking to
reduce organic and inorganic HAP
emissions by approximately 58 tons
each year. These avoided emissions will
result in improvements in air quality
and reduced negative health effects
associated with exposure to air
pollution of these emissions. However,
we have not quantified or monetized the
benefits of reducing these emissions for
this rulemaking because the estimated
costs for this action are less than $100
million.
VI. Request for Comments
We solicit comments on all aspects of
this proposed action. In addition to
general comments on this proposed
action, we are also interested in
additional data that may improve the
risk assessments and other analyses. We
are specifically interested in receiving
any improvements to the data used in
the site-specific emissions profiles used
for risk modeling. Such data should
include supporting documentation in
sufficient detail to allow
characterization of the quality and
representativeness of the data or
information. Section VII of this
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19:34 Feb 13, 2015
Jkt 235001
preamble provides more information on
submitting data.
VII. Submitting Data Corrections
The site-specific emissions profiles
used in the source category risk and
demographic analyses and instructions
are available for download on the RTR
Web site at: https://www.epa.gov/ttn/
atw/rrisk/rtrpg.html. The data files
include detailed information for each
HAP emissions release point for the
facilities in the source category.
If you believe that the data are not
representative or are inaccurate, please
identify the data in question, provide
your reason for concern and provide any
‘‘improved’’ data that you have, if
available. When you submit data, we
request that you provide documentation
of the basis for the revised values to
support your suggested changes. To
submit comments on the data
downloaded from the RTR page,
complete the following steps:
1. Within this downloaded file, enter
suggested revisions to the data fields
appropriate for that information.
2. Fill in the commenter information
fields for each suggested revision (i.e.,
commenter name, commenter
organization, commenter email address,
commenter phone number and revision
comments).
3. Gather documentation for any
suggested emissions revisions (e.g.,
performance test reports, material
balance calculations, etc.).
4. Send the entire downloaded file
with suggested revisions in Microsoft®
Access format and all accompanying
documentation to Docket ID No. EPA–
HQ–OAR–2014–0830 (through one of
the methods described in the ADDRESSES
section of this preamble).
5. If you are providing comments on
a single facility or multiple facilities,
you need only submit one file for all
facilities. The file should contain all
suggested changes for all sources at that
facility. We request that all data revision
comments be submitted in the form of
updated Microsoft® Excel files that are
generated by the Microsoft® Access file.
These files are provided on the RTR
Web site at: https://www.epa.gov/ttn/
atw/rrisk/rtrpg.html.
VIII. Statutory and Executive Order
Reviews
Additional information about these
statutes and Executive Orders can be
found at https://www2.epa.gov/lawsregulations/laws-and-executive-orders.
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A. Executive Order 12866: Regulatory
Planning and Review and Executive
Order 13563: Improving Regulation and
Regulatory Review
This action is not a significant
regulatory action and was therefore not
submitted to the OMB for review.
B. Paperwork Reduction Act (PRA)
The information collection activities
in this proposed rule have been
submitted for approval to the OMB
under the PRA. The ICR document that
the EPA prepared has been assigned
EPA ICR number 1687.10. You can find
a copy of the ICR in the docket for this
rule, and it is briefly summarized here.
Respondents are owners or operators
of aerospace manufacturing and rework
operations. The proposed rule would
add recordkeeping and reporting
provisions for specialty coating
operations, but would not change the
recordkeeping and reporting provisions
for any other types of operations.
Therefore, of the 144 Aerospace
Manufacturing and Rework Facilities
subject to the Aerospace NESHAP, the
annual costs for increased
recordkeeping and reporting would
apply to only the 109 Aerospace
Manufacturing and Rework Facilities
that reported having specialty coating
operations. Respondents must keep
records of the specialty coatings used at
the facility, including the name and
VOC content of the coating, the HAP
and VOC emitted per gallon of coating
and the monthly volume of each coating
used. Respondents must also submit
semiannual reports of noncompliance.
Recordkeeping and reporting of
monitored parameters related to air
pollution control technologies is
required if controls are used to
demonstrate compliance with the
standards. The reports and records will
be used to determine compliance with
the standards.
Respondents/affected entities:
Aerospace manufacturing and rework
facilities using specialty coatings.
Respondent’s obligation to respond:
Mandatory (40 CFR part 63, subpart
GG).
Estimated number of respondents:
109 facilities using specialty coatings.
Frequency of response: Initially,
occasionally and semiannually.
Total estimated burden: 6,914 hours
(per year) for the responding facilities
and 148 hours (per year) for the agency.
These are estimates for the average
annual burden for the first 3 years after
the rule is final. Burden is defined at 5
CFR 1320.3(b).
Total estimated cost: $695,570 (per
year), which includes no annualized
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capital or operation and maintenance
costs, for the responding facilities and
$8,740 (per year) for the agency. These
are estimates for the average annual cost
for the first 3 years after the rule is final.
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 the EPA’s regulations in 40
CFR are listed in 40 CFR part 9. 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, the EPA has
established a public docket for this rule,
which includes this ICR, under Docket
ID No. EPA–HQ–OAR–2014–0830.
Submit your comments on the
Agency’s need for this information, the
accuracy of the provided burden
estimates and any suggested methods
for minimizing respondent burden to
the EPA using the docket identified at
the beginning of this rule. You may also
send your ICR-related comments to
OMB’s Office of Information and
Regulatory Affairs via email to oria_
submissions@omb.eop.gov, Attention:
Desk Officer for the EPA. Since OMB is
required to make a decision concerning
the ICR between 30 and 60 days after
receipt, OMB must receive comments no
later than March 19, 2015. The EPA will
respond to any ICR-related comments in
the final rule.
tkelley on DSK3SPTVN1PROD with PROPOSALS2
C. Regulatory Flexibility Act (RFA)
I certify that this action will not have
a significant economic impact on a
substantial number of small entities
under the RFA. This action will not
impose any requirements on small
entities. No facilities meeting the Small
Business Administration’s definition of
a small business would face significant
control costs, based on the economic
impact analysis completed for this
action. The results of this analysis are
summarized in section V.D of this
preamble and can be found in the
memorandum, Economic Impact
Analysis for Proposed National
Emission Standards for Aerospace
Manufacturing and Rework Facilities,
December 3, 2014. A copy of this
memorandum is in the docket for this
rulemaking.
D. Unfunded Mandates Reform Act
(UMRA)
This action does not contain an
unfunded mandate of $100 million or
more as described in the UMRA, 2
U.S.C. 1531–1538, and does not
significantly or uniquely affect small
governments. The action imposes no
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enforceable duty on any state, local or
tribal governments or the private sector.
E. Executive Order 13132: Federalism
This action 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.
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
This action does not have tribal
implications as specified in Executive
Order 13175. No tribal facilities are
known to be engaged in the aerospace
manufacturing or rework surface coating
operations that would be affected by
this action. Thus, Executive Order
13175 does not apply to this action.
G. Executive Order 13045: Protection of
Children From Environmental Health
Risks and Safety Risks
This action is not subject to Executive
Order 13045 because it is not
economically significant as defined in
Executive Order 12866, and because the
EPA does not believe the environmental
health or safety risks addressed by this
action present a disproportionate risk to
children. This action’s health and risk
assessments are contained in sections
III.A and B and sections IV.B and C of
this preamble.
H. Executive Order 13211: Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution or Use
This action is not subject to Executive
Order 13211 because it is not a
significant regulatory action under
Executive Order 12866.
I. National Technology Transfer and
Advancement Act (NTTAA)
This rulemaking does not involve
technical standards.
J. Executive Order 12898: Federal
Actions to Address Environmental
Justice in Minority Populations and
Low-Income Populations
The EPA believes the human health or
environmental risk addressed by this
action will not have potential
disproportionately high and adverse
human health or environmental effects
on minority, low-income or indigenous
populations.
These proposed standards will
improve public health and welfare, now
and in the future, by reducing HAP
emissions contributing to environmental
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8429
and human health impacts. These
reductions in HAP associated with the
rule are expected to benefit all
populations.
To examine the potential for any
environmental justice issues that might
be associated with the Aerospace
Manufacturing and Rework source
category, we evaluated the distributions
of HAP related cancer and non-cancer
risks across different social,
demographic and economic groups
within the populations living near the
facilities where this source category is
located. The methods used to conduct
demographic analyses for this proposed
rule are described in the document, Risk
and Technology Review—Analysis of
Socio-Economic Factors for Populations
Living Near Aerospace Facilities, which
may be found in the docket for this
rulemaking (Docket ID No. EPA–HQ–
OAR–2014–0830).
In the demographics analysis, we
focused on populations within 50 km of
the facilities in this source category with
emissions sources subject to the MACT
standard. More specifically, for these
populations, we evaluated exposures to
HAP that could result in cancer risks of
1-in-1 million or greater. We compared
the percentages of particular
demographic groups within the focused
populations to the total percentages of
those demographic groups nationwide.
The results of this analysis are
documented in the document, Risk and
Technology Review—Analysis of SocioEconomic Factors for Populations Living
Near Aerospace Facilities.
List of Subjects in 40 CFR Part 63
Environmental protection, Air
pollution control, Hazardous
substances, Reporting and
recordkeeping requirements.
Dated: January 22, 2015.
Gina McCarthy,
Administrator.
For the reasons stated in the
preamble, part 63 of title 40, chapter I,
of the Code of Federal Regulations is
proposed to be amended as follows:
PART 63—NATIONAL EMISSION
STANDARDS FOR HAZARDOUS AIR
POLLUTANTS FOR SOURCE
CATEGORIES
1. The authority citation for part 63
continues to read as follows:
■
Authority: 42 U.S.C. 7401, et seq.
Subpart GG—National Emission
Standards for Aerospace
Manufacturing and Rework Facilities
■
2. Section 63.741 is amended by:
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a. Revising paragraph (c) introductory
text;
■ b. Redesignating paragraphs (c)(4)
through (c)(7) as paragraphs (c)(5)
through (c)(8);
■ c. Adding new paragraph (c)(4);
■ d. Revising newly redesignated
paragraph (c)(8); and
■ e. Revising paragraphs (f) and (g).
The revisions and addition read as
follows:
■
§ 63.741 Applicability and designation of
affected sources.
tkelley on DSK3SPTVN1PROD with PROPOSALS2
*
*
*
*
*
(c) Affected sources. The affected
sources to which the provisions of this
subpart apply are specified in
paragraphs (c)(1) through (8) of this
section. The activities subject to this
subpart are limited to the manufacture
or rework of aerospace vehicles or
components as defined in this subpart.
Where a dispute arises relating to the
applicability of this subpart to a specific
activity, the owner or operator shall
demonstrate whether or not the activity
is regulated under this subpart.
*
*
*
*
*
(4) For organic HAP or VOC
emissions, each specialty coating
application operation, which is the total
of all specialty coating applications at
the facility.
*
*
*
*
*
(8) For inorganic HAP emissions, each
spray booth or hangar that contains a
primer, topcoat or specialty coating
application operation subject to
§ 63.745(g), or a depainting operation
subject to § 63.746(b)(4).
*
*
*
*
*
(f) This subpart does not regulate
research and development, quality
control and laboratory testing activities,
chemical milling, metal finishing,
electrodeposition (except for
electrodeposition of paints), composites
processing (except for cleaning and
coating of composite parts or
components that become part of an
aerospace vehicle or component as well
as composite tooling that comes in
contact with such composite parts or
components prior to cure), electronic
parts and assemblies (except for
cleaning and topcoating of completed
assemblies), manufacture of aircraft
transparencies and wastewater
operations at aerospace facilities. These
requirements do not apply to the rework
of aircraft or aircraft components if the
holder of the Federal Aviation
Administration (FAA) design approval,
or the holder’s licensee, is not actively
manufacturing the aircraft or aircraft
components. These requirements also
do not apply to parts and assemblies not
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Jkt 235001
critical to the vehicle’s structural
integrity or flight performance. The
requirements of this subpart also do not
apply to primers, topcoats, specialty
coatings, chemical milling maskants,
strippers and cleaning solvents
containing HAP and VOC at
concentrations less than 0.1 percent by
mass for carcinogens or 1.0 percent by
mass for noncarcinogens, as determined
from manufacturer’s representations,
such as in a material safety data sheet
or product data sheet or testing.
Additional specific exemptions from
regulatory coverage are set forth in
paragraphs (e), (g), (h), (i) and (j) of this
section and §§ 63.742, 63.744(a)(1), (b),
(e), 63.745(a), (f)(3), (g)(4), 63.746(a),
(b)(5), 63.747(c)(3) and 63.749(d).
(g) The requirements for primers,
topcoats, specialty coatings and
chemical milling maskants in §§ 63.745
and 63.747 do not apply to the use of
low-volume coatings in these categories
for which the annual total of each
separate formulation used at a facility
does not exceed 189 liters (50 gal), and
the combined annual total of all such
primers, topcoats, specialty coatings and
chemical milling maskants used at a
facility does not exceed 757 liters (200
gal). Primers, topcoats and specialty
coatings exempted under paragraph (f)
of this section and under § 63.745(f)(3)
and (g)(4) are not included in the 50 and
200 gal limits. Chemical milling
maskants exempted under § 63.747(c)(3)
are also not included in these limits.
*
*
*
*
*
■ 3. Section 63.742 is amended by
revising the definitions for ‘‘Chemical
milling maskant’’; ‘‘Softener’’; and
‘‘Stripper’’ to read as follows:
§ 63.742
Definitions.
*
*
*
*
*
Chemical milling maskant means a
coating that is applied directly to
aluminum components to protect
surface areas when chemical milling the
component with a Type I or Type II
etchant. Type I chemical milling
maskants are used with a Type I etchant
and Type II chemical milling maskants
are used with a Type II etchant. This
definition does not include bonding
maskants, critical use and line sealer
maskants and seal coat maskants.
Additionally, maskants that must be
used with a combination of Type I or II
etchants and any of the above types of
maskants (i.e., bonding, critical use and
line sealer and seal coat) are also not
included in this definition. (See also
Type I and Type II etchant definitions.)
*
*
*
*
*
Softener means a liquid that is
applied to an aerospace vehicle or
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Fmt 4701
Sfmt 4702
component to degrade coatings such as
primers, topcoats and specialty coatings
specifically as a preparatory step to
subsequent depainting by non-chemical
based depainting equipment. Softeners
may contain VOC, but shall not contain
any HAP as determined from MSDS’s or
manufacturer supplied information.
*
*
*
*
*
Stripper means a liquid that is applied
to an aerospace vehicle or component to
remove permanent coatings such as
primers, topcoats and specialty coatings.
*
*
*
*
*
■ 4. Section 63.743 is amended by:
■ a. Revising paragraphs (a)(2), (8), and
(10);
■ b. Removing and reserving paragraph
(b);
■ c. Revising paragraphs (d)(1), (2), and
(3);
■ d. Removing and reserving paragraphs
(d)(4) and (5);
■ e. Adding paragraph (e).
The revisions and addition read as
follows:
§ 63.743
Standards: General.
(a) * * *
(2) § 63.5, Preconstruction review and
notification requirements; and
*
*
*
*
*
(8) For the purposes of this subpart,
each owner or operator is to be provided
30 calendar days to present additional
information to the Administrator after
he/she is notified of the intended denial
of a compliance extension request
submitted under either § 63.6(i)(4) or
(5), rather than 15 calendar days as
provided for in § 63.6(i)(12)(iii)(B) and
§ 63.6(i)(13)(iii)(B).
*
*
*
*
*
(10) For the purposes of compliance
with the requirements of § 63.5(b)(4) of
the General Provisions and this subpart,
owners or operators of existing primer,
topcoat or specialty coating application
operations and depainting operations
who construct or reconstruct a spray
booth or hangar that does not have the
potential to emit 10 tons/yr or more of
an individual inorganic HAP or 25 tons/
yr or more of all inorganic HAP
combined shall only be required to
notify the Administrator of such
construction or reconstruction on an
annual basis. Notification shall be
submitted on or before March 1 of each
year and shall include the information
required in § 63.5(b)(4) for each such
spray booth or hangar constructed or
reconstructed during the prior calendar
year, except that such information shall
be limited to inorganic HAP’s. No
advance notification or written approval
from the Administrator pursuant to
§ 63.5(b)(3) shall be required for the
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construction or reconstruction of such a
spray booth or hangar unless the booth
or hangar has the potential to emit 10
tons/yr or more of an individual
inorganic HAP or 25 tons/yr or more of
all inorganic HAP combined.
*
*
*
*
*
(d) * * *
(1) Each owner or operator of a new
or existing source shall use any
combination of primers, topcoats
(including self-priming topcoats),
specialty coatings, Type I chemical
milling maskants or Type II chemical
milling maskants such that the monthly
volume-weighted average organic HAP
and VOC contents of the combination of
primers, topcoats, specialty coatings,
Type I chemical milling maskants or
Type II chemical milling maskants, as
determined in accordance with the
applicable procedures set forth in
§ 63.750, complies with the specified
content limits in §§ 63.745(c) and
63.747(c), unless the permitting agency
specifies a shorter averaging period as
part of an ambient ozone control
program.
(2) Averaging is allowed only for
uncontrolled primers, topcoats
(including self-priming topcoats),
specialty coatings, Type I chemical
milling maskants or Type II chemical
milling maskants.
(3) Averaging is not allowed between
specialty coating types defined in
Appendix A to this subpart, or between
the different types of coatings specified
in paragraphs (d)(3)(i) through (vii) of
this section.
(i) Primers and topcoats (including
self-priming topcoats).
(ii) Type I and Type II chemical
milling maskants.
(iii) Primers and chemical milling
maskants.
(iv) Topcoats and chemical milling
maskants.
(v) Primers and specialty coatings.
(vi) Topcoats and specialty coatings.
(vii) Chemical milling maskants and
specialty coatings.
*
*
*
*
*
(e) At all times, the owner or operator
must operate and maintain any affected
source, including associated air
pollution control equipment and
monitoring equipment, in a manner
consistent with safety and good air
pollution control practices for
minimizing emissions. The general duty
to minimize emissions does not require
the owner or operator to make any
further efforts to reduce emissions if
levels required by the applicable
standard have been achieved.
Determination of whether a source is
operating in compliance with operation
and maintenance requirements will be
based on information available to the
Administrator which may include, but
is not limited to, monitoring results,
review of operation and maintenance
procedures, review of operation and
maintenance records and inspection of
the source.
■ 5. Section 63.744 is amended by:
■ a. Revising paragraph (a) introductory
text; and
■ b. Correcting the numerical order of
paragraphs (a)(3) and (4).
The revision reads as follows:
§ 63.744
Standards: Cleaning operations.
(a) Housekeeping measures. Each
owner or operator of a new or existing
cleaning operation subject to this
subpart shall comply with the
requirements in paragraphs (a)(1)
through (4) of this section unless the
cleaning solvent used is identified in
Table 1 of this section or contains HAP
and VOC below the de minimis levels
specified in § 63.741(f).
*
*
*
*
*
■ 6. Section 63.745 is amended by:
■ a. Revising the section heading;
■ b. Revising paragraphs (a), (b), and (c)
introductory text;
■ c. Adding paragraphs (c)(5), (c)(6) and
Table 1;
■ d. Revising paragraphs (e)
introductory text and (e)(1);
8431
e. Revising paragraphs (f) introductory
text, (f)(1) introductory text and (f)(2);
■ f. Revising paragraphs (g) introductory
text, (g)(2)(i), (g)(2)(ii), and (g)(2)(iii)(B).
The revisions and additions read as
follows:
■
§ 63.745 Standards: Primer, topcoat and
specialty coating application operations.
(a) Each owner or operator of a new
or existing primer, topcoat or specialty
coating application operation subject to
this subpart shall comply with the
requirements specified in paragraph (c)
of this section for those coatings that are
uncontrolled (no control device is used
to reduce organic HAP emissions from
the operation), and in paragraph (d) of
this section for those coatings that are
controlled (organic HAP emissions from
the operation are reduced by the use of
a control device). Aerospace equipment
that is no longer operational, intended
for public display and not easily capable
of being moved is exempt from the
requirements of this section.
(b) Each owner or operator shall
conduct the handling and transfer of
primers, topcoats and specialty coatings
to or from containers, tanks, vats,
vessels and piping systems in such a
manner that minimizes spills.
(c) Uncontrolled coatings—organic
HAP and VOC content levels. Each
owner or operator shall comply with the
organic HAP and VOC content limits
specified in paragraphs (c)(1) through
(6) of this section for those coatings that
are uncontrolled.
*
*
*
*
*
(5) Organic HAP emissions from
specialty coatings shall be limited to an
organic HAP content level of no more
than the HAP content limit specified in
Table 1 of this section for each
applicable specialty coating type.
(6) VOC emissions from specialty
coatings shall be limited to a VOC
content level of no more than the VOC
content limit specified in Table 1 of this
section for each applicable specialty
coating type.
TABLE 1—SPECIALTY COATINGS—HAP AND VOC CONTENT LIMITS
tkelley on DSK3SPTVN1PROD with PROPOSALS2
Coating type
HAP limit g/L
(lb/gallon) 1
VOC Limit g/L
(lb/gallon) 1
Ablative Coating .......................................................................................................................................................
Adhesion Promoter ..................................................................................................................................................
Adhesive Bonding Primers: Cured at 250 °F or below ...........................................................................................
Adhesive Bonding Primers: Cured above 250 °F ...................................................................................................
Commercial Interior Adhesive .................................................................................................................................
Cyanoacrylate Adhesive ..........................................................................................................................................
Fuel Tank Adhesive .................................................................................................................................................
Nonstructural Adhesive ............................................................................................................................................
Rocket Motor Bonding Adhesive .............................................................................................................................
Rubber-based Adhesive ..........................................................................................................................................
Structural Autoclavable Adhesive ............................................................................................................................
Structural Nonautoclavable Adhesive ......................................................................................................................
600
890
850
1,030
760
1,020
620
360
890
850
60
850
600
890
850
1,030
760
1,020
620
360
890
850
60
850
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E:\FR\FM\17FEP2.SGM
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(5.0)
(7.4)
(7.1)
(8.6)
(6.3)
(8.5)
(5.2)
(3.0)
(7.4)
(7.1)
(0.5)
(7.1)
(5.0)
(7.4)
(7.1)
(8.6)
(6.3)
(8.5)
(5.2)
(3.0)
(7.4)
(7.1)
(0.5)
(7.1)
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TABLE 1—SPECIALTY COATINGS—HAP AND VOC CONTENT LIMITS—Continued
HAP limit g/L
(lb/gallon) 1
Coating type
Antichafe Coating ....................................................................................................................................................
Bearing Coating .......................................................................................................................................................
Caulking and Smoothing Compounds .....................................................................................................................
Chemical Agent-Resistant Coating ..........................................................................................................................
Clear Coating ...........................................................................................................................................................
Commercial Exterior Aerodynamic Structure Primer ..............................................................................................
Compatible Substrate Primer ..................................................................................................................................
Corrosion Prevention Compound ............................................................................................................................
Cryogenic Flexible Primer .......................................................................................................................................
Cryoprotective Coating ............................................................................................................................................
Dry Lubricative Material ...........................................................................................................................................
Electric or Radiation-Effect Coating ........................................................................................................................
Electrostatic Discharge and Electromagnetic Interference (EMI) Coating ..............................................................
Elevated-Temperature Skydrol-Resistant Commercial Primer ................................................................................
Epoxy Polyamide Topcoat .......................................................................................................................................
Fire-Resistant (interior) Coating ..............................................................................................................................
Flexible Primer .........................................................................................................................................................
Flight-Test Coatings: Missile or Single Use Aircraft ................................................................................................
Flight-Test Coatings: All Other ................................................................................................................................
Fuel-Tank Coating ...................................................................................................................................................
High-Temperature Coating ......................................................................................................................................
Insulation Covering ..................................................................................................................................................
Intermediate Release Coating .................................................................................................................................
Lacquer ....................................................................................................................................................................
Bonding Maskant .....................................................................................................................................................
Critical Use and Line Sealer Maskant .....................................................................................................................
Seal Coat Maskant ..................................................................................................................................................
Metalized Epoxy Coating .........................................................................................................................................
Mold Release ...........................................................................................................................................................
Optical Anti-Reflective Coating ................................................................................................................................
Part Marking Coating ...............................................................................................................................................
Pretreatment Coating ...............................................................................................................................................
Rain Erosion-Resistant Coating ..............................................................................................................................
Rocket Motor Nozzle Coating ..................................................................................................................................
Scale Inhibitor ..........................................................................................................................................................
Screen Print Ink .......................................................................................................................................................
Extrudable/Rollable/Brushable Sealant ...................................................................................................................
Sprayable Sealant ...................................................................................................................................................
Silicone Insulation Material ......................................................................................................................................
Solid Film Lubricant .................................................................................................................................................
Specialized Function Coating ..................................................................................................................................
Temporary Protective Coating .................................................................................................................................
Thermal Control Coating .........................................................................................................................................
Wet Fastener Installation Coating ...........................................................................................................................
Wing Coating ...........................................................................................................................................................
660 (5.5)
620 (5.2)
850 (7.1)
550 (4.6)
720 (6.0)
650 (5.4)
780 (6.5)
710 (5.9)
645 (5.4)
600 (5.0)
880 (7.3)
800 (6.7)
800 (6.7)
740 (6.2)
660 (5.5)
800 (6.7)
640 (5.3)
420 (3.5)
840 (7.0)
720 (6.0)
850 (7.1)
740 (6.2)
750 (6.3)
830 (6.9)
1,230 (10.3)
1,020 (8.5)
1,230 (10.3)
740 (6.2)
780 (6.5)
750 (6.3)
850 (7.1)
780 (6.5)
850 (7.1)
660 (5.5)
880 (7.3)
840 (7.0)
280 (2.3)
600 (5.0)
850 (7.1)
880 (7.3)
890 (7.4)
320 (2.7)
800 (6.7)
675 (5.6)
850 (7.1)
VOC Limit g/L
(lb/gallon) 1
660 (5.5)
620 (5.2)
850 (7.1)
550 (4.6)
720 (6.0)
650 (5.4)
780 (6.5)
710 (5.9)
645 (5.4)
600 (5.0)
880 (7.3)
800 (6.7)
800 (6.7)
740 (6.2)
660 (5.5)
800 (6.7)
640 (5.3)
420 (3.5)
840 (7.0)
720 (6.0)
850 (7.1)
740 (6.2)
750 (6.3)
830 (6.9)
1,230 (10.3)
1,020 (8.5)
1,230 (10.3)
740 (6.2)
780 (6.5)
750 (6.3)
850 (7.1)
780 (6.5)
850 (7.1)
660 (5.5)
880 (7.3)
840 (7.0)
280 (2.3)
600 (5.0)
850 (7.1)
880 (7.3)
890 (7.4)
320 (2.7)
800 (6.7)
675 (5.6)
850 (7.1)
1 Coating limits for HAP are expressed in terms of mass (grams or pounds) of HAP per volume (liters or gallons) of coating less water. Coating
limits for VOC are expressed in terms of mass (grams or pounds) of VOC per volume (liters or gallons) of coating less water and less exempt
solvent.
tkelley on DSK3SPTVN1PROD with PROPOSALS2
*
*
*
*
*
(e) Compliance methods. Compliance
with the organic HAP and VOC content
limits specified in paragraphs (c)(1)
through (6) of this section shall be
accomplished by using the methods
specified in paragraphs (e)(1) and (2) of
this section either by themselves or in
conjunction with one another.
(1) Use primers, topcoats (including
self-priming topcoats) and specialty
coatings with HAP and VOC content
levels equal to or less than the limits
specified in paragraphs (c)(1) through
(6) of this section; or
*
*
*
*
*
(f) Application equipment. Except as
provided in paragraph (f)(3) of this
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section, each owner or operator of a new
or existing primer, topcoat (including
self-priming topcoat) or specialty
coating application operation subject to
this subpart in which any of the
coatings contain organic HAP or VOC
shall comply with the requirements
specified in paragraphs (f)(1) and (2) of
this section.
(1) All primers, topcoats (including
self-priming topcoats) and specialty
coatings shall be applied using one or
more of the application techniques
specified in paragraphs (f)(1)(i) through
(ix) of this section.
*
*
*
*
*
(2) All application devices used to
apply primers, topcoats (including self-
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priming topcoats) or specialty coatings
shall be operated according to company
procedures, local specified operating
procedures and/or the manufacturer’s
specifications, whichever is most
stringent, at all times. Equipment
modified by the facility shall maintain
a transfer efficiency equivalent to HVLP
and electrostatic spray application
techniques.
*
*
*
*
*
(g) Inorganic HAP emissions. Except
as provided in paragraph (g)(4) of this
section, each owner or operator of a new
or existing primer, topcoat or specialty
coating application operation subject to
this subpart in which any of the
coatings that are spray applied contain
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inorganic HAP, shall comply with the
applicable requirements in paragraphs
(g)(1) through (3) of this section.
*
*
*
*
*
(2) * * *
(i) For existing sources, the owner or
operator must choose one of the
following:
(A) Before exhausting it to the
atmosphere, pass the air stream through
a dry particulate filter system certified
using the methods described in
§ 63.750(o) to meet or exceed the
efficiency data points in Tables 2 and 3
of this section; or
(C) Before exhausting it to the
atmosphere, pass the air stream through
an air pollution control system that
meets or exceeds the efficiency data
points in Tables 2 and 3 of this section
and is approved by the permitting
authority.
TABLE 2—TWO-STAGE ARRESTOR;
LIQUID PHASE CHALLENGE FOR EXISTING SOURCES
Filtration efficiency
requirement, %
Aerodynamic
particle size
range, μm
>90 ........................................
>50 ........................................
>10 ........................................
>5.7
>4.1
>2.2
TABLE 4—THREE-STAGE ARRESTOR; ■ e. Revising paragraph (e) introductory
LIQUID PHASE CHALLENGE FOR NEW text;
■ f. Adding paragraph (j).
SOURCES
Aerodynamic
particle size
range, μm
Filtration efficiency
requirement, %
>95 ......................................
>80 ......................................
>65 ......................................
>2.0
>1.0
>0.42
TABLE 5—THREE-STAGE ARRESTOR;
SOLID PHASE CHALLENGE FOR NEW
SOURCES
Aerodynamic
particle size
range, μm
Filtration efficiency
requirement, %
>95 ......................................
>85 ......................................
>75 ......................................
>2.5
>1.1
>0.70
(iii) * * *
(B) If the primer, topcoat or specialty
coating contains chromium or cadmium,
control shall consist of a HEPA filter
system, three-stage filter system or other
control system equivalent to the three
stage filter system as approved by the
permitting agency.
*
*
*
*
*
■ 7. Section 63.746 is amended by
revising (b)(4)(ii)(A) and (B) to read as
follows:
§ 63.746 Standards: Depainting
operations.
TABLE 3—TWO-STAGE ARRESTOR;
*
*
*
SOLID PHASE CHALLENGE FOR EX(b) * * *
ISTING SOURCES
(4) * * *
Filtration efficiency
requirement, %
Aerodynamic
particle size
range, μm
tkelley on DSK3SPTVN1PROD with PROPOSALS2
>90 ........................................
>50 ........................................
>10 ........................................
>8.1
>5.0
>2.6
(ii) For new sources, either:
(A) Before exhausting it to the
atmosphere, pass the air stream through
a dry particulate filter system certified
using the methods described in
§ 63.750(o) to meet or exceed the
efficiency data points in Tables 4 and 5
of this section; or (B) Before exhausting
it to the atmosphere, pass the air stream
through an air pollution control system
that meets or exceeds the efficiency data
points in Tables 4 and 5 of this section
and is approved by the permitting
authority.
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*
*
(ii)(A) For existing sources, pass any
air stream removed from the enclosed
area or closed-cycle depainting system
through a dry particulate filter system,
certified using the method described in
§ 63.750(o) to meet or exceed the
efficiency data points in Tables 2 and 3
of § 63.745, through a baghouse or
through a waterwash system before
exhausting it to the atmosphere.
(B) For new sources, pass any air
stream removed from the enclosed area
or closed-cycle depainting system
through a dry particulate filter system
certified using the method described in
§ 63.750(o) to meet or exceed the
efficiency data points in Tables 4 and 5
of § 63.745 or through a baghouse before
exhausting it to the atmosphere.
*
*
*
*
*
■ 8. Section 63.749 is amended by:
■ a. Revising paragraphs (a)(1) and (2);
■ b. Adding paragraph (a)(3);
■ c. Revising paragraph (b);
■ d. Revising the heading of paragraph
(d), paragraph (d)(4) introductory text
and paragraph (d)(4)(i);
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The revisions and additions read as
follows:
§ 63.749 Compliance dates and
determinations.
(a) * * * (1) Each owner or operator
of an existing affected source subject to
this subpart shall comply with the
requirements of this subpart by
September 1, 1998, except as specified
in paragraphs (a)(2) and (3) of this
section. Owners or operators of new
affected sources subject to this subpart
shall comply on the effective date or
upon startup, whichever is later. In
addition, each owner or operator shall
comply with the compliance dates
specified in § 63.6(b) and (c) as
indicated in Table 1 to subpart GG of
part 63.
(2) Owners or operators of existing
primer, topcoat or specialty coating
application operations and depainting
operations who construct or reconstruct
a spray booth or hangar must comply
with the new source requirements for
inorganic HAP specified in
§§ 63.745(g)(2)(ii) and 63.746(b)(4) for
that new spray booth or hangar upon
startup. Such sources must still comply
with all other existing source
requirements by September 1, 1998.
(3) Each owner or operator of a
specialty coating application operation
that begins construction or
reconstruction after [date of publication
of final rule in the Federal Register]
shall be in compliance with the
requirements of this subpart on [date of
publication of final rule in the Federal
Register] or upon startup, whichever is
later. Each owner or operator of a
specialty coating application operation
that is existing on [date of publication
of final rule in the Federal Register]
shall be in compliance with the
requirements of this subpart on or
before [date 1 year after date of
publication of final rule in the Federal
Register].
(b) General. Each facility subject to
this subpart shall be considered in
noncompliance if the owner or operator
fails to use a control device other than
one specified in this subpart that has
not been approved by the
Administrator, as required by
§ 63.743(c).
*
*
*
*
*
(d) Organic HAP and VOC content
levels—primer, topcoat and specialty
coating application operations —
*
*
*
*
*
(4) The topcoat or specialty coating
application operation is considered in
compliance when the conditions
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8434
Federal Register / Vol. 80, No. 31 / Tuesday, February 17, 2015 / Proposed Rules
specified in paragraphs (d)(4)(i) through
(iv) of this section, as applicable, and in
paragraph (e) of this section are met.
Failure to meet any of the conditions
identified in these paragraphs shall
constitute noncompliance.
(i) The topcoat application operation
is considered in compliance when the
conditions specified in paragraphs
(d)(4)(i)(A) are met. The specialty
coating application operation is
considered in compliance when the
conditions specified in paragraphs
(d)(4)(i)(B) are met.
(A) For all uncontrolled topcoats, all
values of Hi and Ha (as determined using
the procedures specified in § 63.750(c)
and (d)) are less than or equal to 420
grams organic HAP per liter (3.5 lb/gal)
of topcoat (less water) as applied, and
all values of Gi and Ga (as determined
using the procedures specified in
§ 63.750(e) and (f)) are less than or equal
to 420 grams organic VOC per liter (3.5
lb/gal) of topcoat (less water and exempt
solvents) as applied.
(B) For all uncontrolled specialty
coatings, all values of Hi and Ha (as
determined using the procedures
specified in § 63.750(c) and (d)) are less
than or equal to the HAP content limits
specified in Table 1 to § 63.745 for the
applicable specialty coating types (less
water) as applied, and all values of Gi
and Ga (as determined using the
procedures specified in § 63.750(e) and
(f)) are less than or equal to the VOC
content limits specified in Table 1 to
§ 63.745 for the applicable specialty
coating types (less water and exempt
solvents) as applied.
*
*
*
*
*
(e) Inorganic HAP emissions—primer,
topcoat and specialty coating
application operations. For each primer,
topcoat or specialty coating application
operation that emits inorganic HAP, the
operation is in compliance when:
*
*
*
*
*
(j) Performance tests shall be
conducted under such conditions as the
Administrator specifies to the owner or
operator based on representative
performance of the affected source for
the period being tested. Representative
conditions exclude periods of startup
and shutdown unless specified by the
Administrator or an applicable subpart.
The owner or operator may not conduct
performance tests during periods of
malfunction. The owner or operator
must record the process information
that is necessary to document operating
conditions during the test and include
in such record an explanation to
support that such conditions represent
normal operation. Upon request, the
owner or operator shall make available
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19:34 Feb 13, 2015
Jkt 235001
to the Administrator such records as
may be necessary to determine the
conditions of performance tests.
■ 9. Section 63.750 is amended by:
■ a. Revising paragraphs (c)
introductory text, (d) introductory text
and (e) introductory text;
■ b. Revising paragraphs (f) introductory
text and (f)(1)(iii);
■ c. Revising paragraph (h)(3)(i)(1); and
■ d. Revising paragraphs (k)
introductory text, (m) introductory text
and (o).
The revisions are as follows:
§ 63.750
Test methods and procedures.
*
*
*
*
*
(c) Organic HAP content level
determination—compliant primers,
topcoats and specialty coatings. For
those uncontrolled primers, topcoats
and specialty coatings complying with
the primer, topcoat or specialty coating
organic HAP content limits specified in
§ 63.745(c) without being averaged, the
procedures in paragraphs (c)(1) through
(3) of this section shall be used to
determine the mass of organic HAP
emitted per volume of coating (less
water) as applied. As an alternative to
the procedures in paragraphs (c)(1)
through (3) of this section, an owner or
operator may use the coating
manufacturer’s supplied data to
demonstrate that organic HAP emitted
per volume of coating (less water), as
applied, is less than or equal to the
applicable organic HAP limit specified
in § 63.745(c).
*
*
*
*
*
(d) Organic HAP content level
determination—averaged primers,
topcoats and specialty coatings. For
those uncontrolled primers, topcoats
and specialty coatings that are averaged
together in order to comply with the
primer, topcoat and specialty coating
organic HAP content limits specified in
§ 63.745(c), the following procedure
shall be used to determine the monthly
volume-weighted average mass of
organic HAP emitted per volume of
coating (less water) as applied, unless
the permitting agency specifies a shorter
averaging period as part of an ambient
ozone control program.
*
*
*
*
*
(e) VOC content level determination—
compliant primers, topcoats and
specialty coatings. For those
uncontrolled primers, topcoats and
specialty coatings complying with the
primer, topcoat and specialty coating
VOC content levels specified in
§ 63.745(c) without being averaged, the
procedures in paragraphs (e)(1) through
(3) of this section shall be used to
determine the mass of VOC emitted per
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Sfmt 4702
volume of coating (less water and
exempt solvents) as applied. As an
alternative to the procedures in
paragraphs (e)(1) through (3) of this
section, an owner or operator may use
coating manufacturer’s supplied data to
demonstrate that VOC emitted per
volume of coating (less water and
exempt solvents), as applied, is less
than or equal to the applicable VOC
limit specified in § 63.745(c).
*
*
*
*
*
(f) VOC content level determination—
averaged primers, topcoats and
specialty coatings. For those
uncontrolled primers, topcoats and
specialty coatings that are averaged
within their respective coating category
in order to comply with the primer,
topcoat and specialty coating VOC
content limits specified in § 63.745
(c)(2), (4), and (6), the following
procedure shall be used to determine
the monthly volume-weighted average
mass of VOC emitted per volume of
coating (less water and exempt solvents)
as applied, unless the permitting agency
specifies a shorter averaging period as
part of an ambient ozone control
program.
(1) * * *
(iii) Determine the VOC content of
each primer, topcoat and specialty
coating formulation (less water and
exempt solvents) as applied using EPA
Method 24 or from manufacturer’s data.
*
*
*
*
*
(h) * * *
(3) * * *
(i)(1) Alternative application
method—primers, topcoats and
specialty coatings. Each owner or
operator seeking to use an alternative
application method (as allowed in
§ 63.745(f)(1)(ix)) in complying with the
standards for primers, topcoats and
specialty coatings shall use the
procedures specified in paragraphs
(i)(2)(i) and (ii) or (iii) of this section to
determine the organic HAP and VOC
emission levels of the alternative
application technique as compared to
either HVLP or electrostatic spray
application methods.
*
*
*
*
*
(k) Organic HAP content level
determination—compliant chemical
milling maskants. For those
uncontrolled chemical milling maskants
complying with the chemical milling
maskant organic HAP content limit
specified in § 63.747(c)(1) without being
averaged, the procedure in paragraph
(k)(1) of this section shall be used to
determine the mass of organic HAP
emitted per unit volume of coating
(chemical milling maskant) i as applied
(less water), Hi (lb/gal). As an alternative
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to the procedures in paragraph (k)(1) of
this section, an owner or operator may
use coating manufacturer’s supplied
data to demonstrate that organic HAP
emitted per volume of coating (less
water), as applied, is less than or equal
to the applicable organic HAP limit
specified in § 63.747(c).
*
*
*
*
*
(m) VOC content level
determination—compliant chemical
milling maskants. For those
uncontrolled chemical milling maskants
complying with the chemical milling
maskant VOC content limit specified in
§ 63.747(c)(2) without being averaged,
the procedure specified in paragraphs
(m)(1) and (2) of this section shall be
used to determine the mass of VOC
emitted per volume of chemical milling
maskant (less water and exempt
solvents) as applied. As an alternative to
the procedures in paragraphs (m)(1) and
(2) of this section, an owner or operator
may use coating manufacturer’s
supplied data to demonstrate that VOC
emitted per volume of coating (less
water and exempt solvents), as applied,
is less than or equal to the applicable
VOC limit specified in § 63.747(c).
*
*
*
*
*
(o) Inorganic HAP emissions—dry
particulate filter certification
requirements. Dry particulate filters
used to comply with § 63.745(g)(2) or
§ 63.746(b)(4) must be certified by the
filter manufacturer or distributor, paint/
depainting booth supplier and/or the
facility owner or operator using method
319 in appendix A of this part, to meet
or exceed the efficiency data points
found in Tables 2 and 3 or 4 and 5 of
§ 63.745 for existing or new sources
respectively.
■ 10. Section 63.751 is amended by
revising paragraph (c) to read as follows:
§ 63.751
Monitoring requirements.
tkelley on DSK3SPTVN1PROD with PROPOSALS2
*
*
*
*
*
(c) Dry particulate filter, HEPA filter
and waterwash systems—primer,
topcoat and specialty coating
application operations. (1) Each owner
or operator using a dry particulate filter
system to meet the requirements of
§ 63.745(g)(2) shall, while primer,
topcoat and specialty coating
application operations are occurring,
continuously monitor the pressure drop
across the system and read and record
the pressure drop once per shift
following the recordkeeping
requirements of § 63.752(d).
(2) Each owner or operator using a
conventional waterwash system to meet
the requirements of § 63.745(g)(2) shall,
while primer or topcoat application
operations are occurring, continuously
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Jkt 235001
monitor the water flow rate through the
system and read and record the water
flow rate once per shift following the
recordkeeping requirements of
§ 63.752(d). Each owner or operator
using a pumpless waterwash system to
meet the requirements of § 63.745(g)(2)
shall, while primer, topcoat and
specialty coating application operations
are occurring, measure and record the
parameter(s) recommended by the booth
manufacturer that indicate booth
performance once per shift, following
the recordkeeping requirements of
§ 63.752(d).
*
*
*
*
*
■ 11. Section 63.752 is amended by:
■ a. Revising paragraph (a);
■ b. Revising paragraphs (c)
introductory text, (c)(1), (c)(2)
introductory text, (c)(4) introductory
text, (c)(5) introductory text and (c)(6)
introductory text;
■ c. Revising paragraphs (d) paragraph
heading and (d)(1); and
■ d. Revising paragraph (f) introductory
text.
The revisions read as follows:
§ 63.752
Recordkeeping requirements.
(a) General. Each owner or operator of
a source subject to this subpart shall
fulfill all recordkeeping requirements
specified in § 63.10 (a), (b), (d) and (f),
except § 63.10(b)(2)(i), (iv), and (v). Each
owner or operator must also record and
maintain according to § 63.10(b)(1) the
information specified in paragraph (a)(1)
through (3) of this section.
(1) In the event that an affected unit
fails to meet an applicable standard,
record the number of failures. For each
failure record the date, time and
duration of each failure.
(2) For each failure to meet an
applicable standard, record and retain a
list of the affected sources or equipment,
an estimate of the quantity of each
regulated pollutant emitted over any
emission limit and a description of the
method used to estimate the emissions.
(3) Record actions taken to minimize
emissions in accordance with
§ 63.743(e), and any corrective actions
taken to return the affected unit to its
normal or usual manner of operation.
*
*
*
*
*
(c) Primer, topcoat and specialty
coating application operations—organic
HAP and VOC. Each owner or operator
required to comply with the organic
HAP and VOC content limits specified
in § 63.745(c) shall record the
information specified in paragraphs
(c)(1) through (6) of this section, as
appropriate. Each owner and operator
using coating manufacturer’s supplied
data to demonstrate compliance with
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8435
the applicable organic HAP or VOC
limit specified in § 63.745(c) may retain
the manufacturer’s documentation and
annual purchase records in place of the
records specified in paragraphs (c)(2)
and (3) of this section.
(1) The name and VOC content as
received and as applied of each primer,
topcoat and specialty coating used at the
facility.
(2) For uncontrolled primers, topcoats
and specialty coatings that meet the
organic HAP and VOC content limits in
§ 63.745(c)(1) through (6) without
averaging:
*
*
*
*
*
(4) For primers, topcoats and specialty
coatings complying with the organic
HAP or VOC content level by averaging:
*
*
*
*
*
(5) For primers, topcoats and specialty
coatings that are controlled by a control
device other than a carbon adsorber:
*
*
*
*
*
(6) For primers, topcoats and specialty
coatings that are controlled by a carbon
adsorber:
*
*
*
*
*
(d) Primer, topcoat and specialty
coating application operations—
inorganic HAP emissions. (1) Each
owner or operator complying with
§ 63.745(g) for the control of inorganic
HAP emissions from primer, topcoat
and specialty coating application
operations through the use of a dry
particulate filter system or a HEPA filter
system shall record the pressure drop
across the operating system once each
shift during which coating operations
occur.
(f) Chemical milling maskant
application operations. Each owner or
operator seeking to comply with the
organic HAP and VOC content limits for
the chemical milling maskant
application operation, as specified in
§ 63.747(c), or the control system
requirements specified in § 63.747(d),
shall record the information specified in
paragraphs (f)(1) through (4) of this
section, as appropriate. Each owner and
operator using coating manufacturer’s
supplied data to demonstrate
compliance with the applicable organic
HAP or VOC limit specified in
§ 63.747(c) may retain the
manufacturer’s documentation and
annual purchase records in place of the
records specified in paragraph (f)(1) of
this section.
*
*
*
*
*
■ 12. Section 63.753 is amended by:
■ a. Revising paragraph (a)(1)
introductory text and (a)(2);
■ b. Adding paragraphs (a)(4) and (5);
■ c. Revising paragraphs (c)
introductory text, (c)(1)(i) and (ii).
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d. Revising paragraph (e)(1).
The revisions and additions read as
follows:
■
§ 63.753
Reporting requirements.
(a)(1) Except as provided in
paragraphs (a)(2) through (5) of this
section, each owner or operator subject
to this subpart shall fulfill the
requirements contained in § 63.9(a)
through (e) and (h) through (j),
Notification requirements and
§ 63.10(a), (b), (d) and (f), Recordkeeping
and reporting requirements, of the
General Provisions, 40 CFR part 63,
subpart A and that the initial
notification for existing sources required
in § 63.9(b)(2) shall be submitted not
later than September 1, 1997, or as
specified in § 63.9(b)(2). In addition to
the requirements of § 63.9(h), the
notification of compliance status shall
include:
*
*
*
*
*
(2) The initial notification for existing
sources, required in § 63.9(b)(2) shall be
submitted no later than September 1,
1997, or as specified in § 63.9(b)(2). For
the purposes of this subpart, a title V or
part 70 permit application may be used
in lieu of the initial notification
required under § 63.9(b)(2), provided
the same information is contained in the
permit application as required by
§ 63.9(b)(2), and the State to which the
permit application has been submitted
has an approved operating permit
program under part 70 of this chapter
and has received delegation of authority
from the EPA. Permit applications shall
be submitted by the same due dates as
those specified for the initial
notifications.
*
*
*
*
*
(4) Each owner or operator subject to
this subpart is not required to comply
with § 63.10(b)(2)(i), (b)(2)(iv), (b)(2)(v),
and (d)(5).
(5) If a source fails to meet an
applicable standard specified in
§§ 63.744 through 63.748, report such
events in the semiannual report:
(i) The number of failures to meet an
applicable standard.
(ii) For each instance, report the date,
time and duration of each failure.
(iii) For each failure the report must
include a list of the affected sources or
equipment, an estimate of the quantity
of each regulated pollutant emitted over
any emission limit and a description of
the method used to estimate the
emissions.
*
*
*
*
*
(c) Primer, topcoat and specialty
coating application operations. Each
owner or operator of a primer or topcoat
application operation subject to this
subpart shall submit the following
information:
(1) * * *
(i) For primers, topcoats and specialty
coatings where compliance is not being
achieved through the use of averaging or
a control device, the HAP or VOC
content in manufacturer’s supplied data
as recorded under § 63.752(c), or each
value of Hi and Gi as recorded under
§ 63.752(c)(2)(i), that exceeds the
applicable organic HAP or VOC content
limit specified in § 63.745(c);
(ii) For primers, topcoats and
specialty coatings where compliance is
being achieved through the use of
averaging, each value of Ha and Ga, as
recorded under § 63.752(c)(4)(i), that
exceeds the applicable organic HAP or
VOC content limit specified in
§ 63.745(c);
*
*
*
*
*
(e) * * *
(1) For chemical milling maskants
where compliance is not being achieved
through the use of averaging or a control
device, the HAP or VOC content in
manufacturer’s supplied data as
recorded under § 63.752(f), or each
value of Hi and Gi as recorded under
§ 63.752(f)(1)(i), that exceeds the
applicable organic HAP or VOC content
limit specified in § 63.747(c);
*
*
*
*
*
■ 13. Revise Table 1 to Subpart GG of
Part 63 to read as follows:
TABLE 1 TO SUBPART GG OF PART 63—GENERAL PROVISIONS APPLICABILITY TO SUBPART GG
tkelley on DSK3SPTVN1PROD with PROPOSALS2
Reference
Applies to affected sources
in subpart GG
63.1(a)(1) ..........................................................................
63.1(a)(2) ..........................................................................
63.1(a)(3) ..........................................................................
63.1(a)(4) ..........................................................................
63.1(a)(5) ..........................................................................
63.1(a)(6) ..........................................................................
63.1(a)(7) ..........................................................................
63.1(a)(8) ..........................................................................
63.1(a)(9) ..........................................................................
63.1(a)(10) ........................................................................
63.1(a)(11) ........................................................................
63.1(a)(12) ........................................................................
63.1(a)(13) ........................................................................
63.1(a)(14) ........................................................................
63.1(b)(1) ..........................................................................
63.1(b)(2) ..........................................................................
63.1(b)(3) ..........................................................................
63.1(c)(1) ..........................................................................
63.1(c)(2) ..........................................................................
63.1(c)(3) ..........................................................................
63.1(c)(4) ..........................................................................
63.1(c)(5) ..........................................................................
63.1(d) ...............................................................................
63.1(e) ...............................................................................
63.2 ...................................................................................
63.3 ...................................................................................
63.4(a)(1) ..........................................................................
63.4(a)(2) ..........................................................................
63.4(a)(3) ..........................................................................
63.4(a)(4) ..........................................................................
63.4(a)(5) ..........................................................................
Yes.
Yes.
Yes.
Yes.
No .......................................
Yes.
Yes.
Yes.
No .......................................
Yes.
Yes.
Yes.
Yes.
Yes.
Yes.
Yes.
Yes.
Yes.
Yes .....................................
No .......................................
Yes.
Yes.
No .......................................
Yes.
Yes.
Yes.
Yes.
Yes.
Yes.
No .......................................
Yes.
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Comment
Reserved.
Reserved.
Subpart GG does not apply to area sources.
Reserved.
Reserved.
Reserved.
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TABLE 1 TO SUBPART GG OF PART 63—GENERAL PROVISIONS APPLICABILITY TO SUBPART GG—Continued
Applies to affected sources
in subpart GG
63.4(b) ...............................................................................
63.4(c) ...............................................................................
63.5(a) ...............................................................................
63.5(b)(1) ..........................................................................
63.5(b)(2) ..........................................................................
63.5(b)(3) ..........................................................................
63.5(b)(4) ..........................................................................
63.5(b)(5) ..........................................................................
63.5(b)(6) ..........................................................................
63.5(c) ...............................................................................
63.5(d)(1)(i) .......................................................................
63.5(d)(1)(ii)(A) through (H) ..............................................
63.5(d)(1)(ii)(I) ...................................................................
63.5(d)(1)(ii)(J) ..................................................................
63.5(d)(1)(iii) .....................................................................
63.5(d)(2) through (4) .......................................................
63.5(e) ...............................................................................
63.5(f) ................................................................................
63.6(a) ...............................................................................
63.6(b)(1) through (5) .......................................................
Yes.
Yes.
Yes.
Yes.
No .......................................
Yes.
Yes.
Yes.
Yes.
No .......................................
Yes.
Yes.
No .......................................
Yes.
Yes.
Yes.
Yes.
Yes.
Yes.
Yes .....................................
63.6(b)(6)
63.6(b)(7)
63.6(c)(1)
63.6(c)(2)
..........................................................................
..........................................................................
..........................................................................
..........................................................................
No .......................................
Yes.
Yes.
No .......................................
63.6(c)(3) and (4) ..............................................................
63.6(c)(5) ..........................................................................
63.6(d) ...............................................................................
63.6(e)(1)(i) .......................................................................
63.6(e)(1)(ii) ......................................................................
63.6(e)(2) ..........................................................................
63.6(e)(3) ..........................................................................
63.6(f)(1) ...........................................................................
63.6(f)(2) and (3) ..............................................................
63.6(g) ...............................................................................
63.6(h) ...............................................................................
No .......................................
Yes.
No .......................................
No .......................................
No.
No .......................................
No.
No.
Yes.
Yes.
No .......................................
63.6(i)(1) and (3) ...............................................................
63.6(i)(4)(i)(A) ...................................................................
63.6(i)(4)(i)(B) ...................................................................
Yes.
Yes.
No .......................................
63.6(i)(4)(ii) .......................................................................
tkelley on DSK3SPTVN1PROD with PROPOSALS2
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No .......................................
63.6(i)(5) through (12) ......................................................
63.6(i)(13) .........................................................................
63.6(i)(14) .........................................................................
63.6(i)(15) .........................................................................
63.6(i)(16) .........................................................................
63.6(j) ................................................................................
63.7(a)(1) ..........................................................................
63.7(a)(2)(i) through (vi) ...................................................
63.7(a)(2)(vii) and (viii) .....................................................
63.7(a)(2)(ix) .....................................................................
63.7(a)(3) ..........................................................................
63.7(b) ...............................................................................
63.7(c) ...............................................................................
63.7(d) ...............................................................................
63.7(e)(1) ..........................................................................
63.7(e)(2) through (4) .......................................................
63.7(f) ................................................................................
63.7(g)(1) ..........................................................................
63.7(g)(2) ..........................................................................
63.7(g)(3) ..........................................................................
63.7(h) ...............................................................................
63.8(a)(1) and (2) .............................................................
63.8(a)(3) ..........................................................................
63.8(a)(4) ..........................................................................
63.8(b) ...............................................................................
63.8(c)(1)(i) .......................................................................
Yes.
Yes.
Yes.
No .......................................
Yes.
Yes.
Yes.
Yes.
No .......................................
Yes.
Yes.
Yes.
Yes.
Yes.
No .......................................
Yes.
Yes.
Yes.
No .......................................
Yes.
Yes.
Yes.
No .......................................
Yes.
Yes.
No.
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Comment
Reserved.
Reserved.
Reserved.
§ 63.749(a)
sources.
Reserved.
specifies
compliance
dates
for
new
The standards in subpart GG are promulgated under
section 112(d) of the CAA.
Reserved.
Reserved.
See § 63.743(e) for general duty requirement.
Section reserved.
The standards in subpart GG do not include opacity
standards.
§ 63.743(a)(4) specifies that requests for extension of
compliance must be submitted no later than 120
days before an affected source’s compliance date.
The standards in subpart GG are promulgated under
section 112(d) of the CAA.
Reserved.
Reserved.
See § 63.749(j).
Reserved.
Reserved.
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TABLE 1 TO SUBPART GG OF PART 63—GENERAL PROVISIONS APPLICABILITY TO SUBPART GG—Continued
Applies to affected sources
in subpart GG
63.8(c)(1)(ii) ......................................................................
63.8(c)(1)(iii) ......................................................................
63.8(c)(2) through (d)(2) ...................................................
63.8(d)(3) ..........................................................................
63.8(e)(1) through (4) .......................................................
63.8(e)(5)(i) .......................................................................
63.8(e)(5)(ii) ......................................................................
Yes.
No.
Yes.
No.
Yes.
Yes.
No .......................................
63.8(f)(1) ...........................................................................
63.8(f)(2)(i) through (vii) ....................................................
63.8(f)(2)(viii) .....................................................................
Yes.
Yes.
No .......................................
63.8(f)(2)(ix) ......................................................................
63.8(f)(3) through (6) ........................................................
63.8(g) ...............................................................................
63.9(a) ...............................................................................
63.9(b)(1) ..........................................................................
63.9(b)(2) ..........................................................................
Yes.
Yes.
Yes.
Yes.
Yes.
Yes .....................................
63.9(b)(3) ..........................................................................
63.9(b)(4) ..........................................................................
63.9(b)(5) ..........................................................................
63.9(c) ...............................................................................
63.9(d) ...............................................................................
63.9(e) ...............................................................................
63.9(f) ................................................................................
Yes.
Yes.
Yes.
Yes.
Yes.
Yes.
No .......................................
63.9(g)(1) ..........................................................................
63.9(g)(2) ..........................................................................
No.
No .......................................
63.9(g)(3) ..........................................................................
63.9(h)(1) through (3) .......................................................
No.
Yes .....................................
63.9(h)(4) ..........................................................................
63.9(h)(5) and (6) .............................................................
63.9(i) ................................................................................
63.9(j) ................................................................................
63.10(a) .............................................................................
63.10(b)(1) ........................................................................
63.10(b)(2)(i) .....................................................................
63.10(b)(2)(ii) ....................................................................
No .......................................
Yes.
Yes.
Yes.
Yes.
Yes.
No.
No .......................................
63.10(b)(2)(iii) ...................................................................
63.10(b)(2)(iv) and (v) .......................................................
63.10(b)(2)(vi) ...................................................................
63.10(b)(2)(vi)(A) through (C) ...........................................
tkelley on DSK3SPTVN1PROD with PROPOSALS2
Reference
Yes.
No.
Yes.
No .......................................
63.10(b)(2)(vii) through (xiv).
63.10(b)(3) ........................................................................
63.10(c)(1) ........................................................................
63.10(c)(2) through (4) .....................................................
63.10(c)(5) and (6) ............................................................
63.10(c)(7) and (8) ............................................................
63.10(c)(9) ........................................................................
63.10(c)(10) through (13) .................................................
63.10(c)(14) ......................................................................
63.10(c)(15) ......................................................................
63.10(d)(1) and (2) ...........................................................
63.10(d)(3) ........................................................................
Yes.
No.
No .......................................
No.
Yes.
No .......................................
No.
No .......................................
No.
Yes.
No .......................................
63.10(d)(4) ........................................................................
63.10(d)(5) ........................................................................
63.(10)(e)(1) ......................................................................
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Comment
The standards in subpart GG do not include opacity
standards.
The standards in subpart GG do not include opacity
standards.
§ 63.753(a)(1) requires submittal of the initial notification at least 1 year prior to the compliance date;
§ 63.753(a)(2) allows a title V or part 70 permit application to be substituted for the initial notification in
certain circumstances.
The standards in subpart GG do not include opacity
standards.
The standards in subpart GG do not include opacity
standards.
§ 63.753(a)(1) also specifies additional information to
be included in the notification of compliance status.
Reserved.
See § 63.752(a) for recordkeeping of: (1) Date, time
and duration; (2) Listing of affected source or equipment and an estimate of the quantity of each regulated pollutant emitted over the standard; and (3) Actions to minimize emissions and correct the failure.
§ 63.10(b)(vii)(A), (B) and (C) do not apply because
subpart GG does not require the use of CEMS.
Reserved.
Reserved.
§ 63.8(d) does not apply to this subpart.
The standards in subpart GG do not include opacity
standards.
Yes.
No. See § 63.753 (a)(5) for
malfunction reporting requirements..
No.
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8439
TABLE 1 TO SUBPART GG OF PART 63—GENERAL PROVISIONS APPLICABILITY TO SUBPART GG—Continued
Reference
Applies to affected sources
in subpart GG
63.10(e)(2)(i) .....................................................................
63.10(e)(2)(ii) ....................................................................
No.
No .......................................
63.10(e)(3) ........................................................................
63.10(e)(4) ........................................................................
No.
No .......................................
63.10(f) ..............................................................................
63.11 .................................................................................
63.12 .................................................................................
63.13 .................................................................................
63.14 .................................................................................
63.15 .................................................................................
63.16 .................................................................................
Yes.
Yes.
Yes.
Yes.
Yes.
Yes.
Yes.
Comment
The standards in subpart GG do not include opacity
standards.
The standards in subpart GG do not include opacity
standards.
[FR Doc. 2015–02055 Filed 2–13–15; 8:45 am]
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Agencies
[Federal Register Volume 80, Number 31 (Tuesday, February 17, 2015)]
[Proposed Rules]
[Pages 8391-8439]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-02055]
[[Page 8391]]
Vol. 80
Tuesday,
No. 31
February 17, 2015
Part II
Environmental Protection Agency
-----------------------------------------------------------------------
40 CFR Part 63
National Emission Standards for Aerospace Manufacturing and Rework
Facilities Risk and Technology Review; Proposed Rule
Federal Register / Vol. 80 , No. 31 / Tuesday, February 17, 2015 /
Proposed Rules
[[Page 8392]]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 63
[EPA-HQ-OAR-2014-0830; FRL-9922-10-OAR]
RIN 2060-AQ99
National Emission Standards for Aerospace Manufacturing and
Rework Facilities Risk and Technology Review
AGENCY: Environmental Protection Agency.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: The Environmental Protection Agency (EPA) is proposing
amendments to the national emissions standards for hazardous air
pollutants (NESHAP) for Aerospace Manufacturing and Rework Facilities
to address the results of the residual risk and technology review (RTR)
conducted as required under the Clean Air Act (CAA), and to correct
errors and deficiencies identified during the review of these
standards. The proposed amendments would add limitations to reduce
organic and inorganic emissions of hazardous air pollutants (HAP) from
specialty coating application operations; would remove the exemptions
from the emission limitations for periods of startup, shutdown and
malfunction (SSM) so that affected units would be subject to the
emission standards at all times; and would revise provisions to address
recordkeeping and reporting requirements applicable to periods of SSM.
This action also proposes other technical corrections. The EPA
estimates that implementation of this proposed rule will result in
reductions of 58 tons of HAP.
DATES: Comments. Comments must be received on or before April 3, 2015.
A copy of comments on the information collection provisions should be
submitted to the Office of Management and Budget (OMB) on or before
March 19, 2015.
Public Hearing. If anyone contacts the EPA requesting a public
hearing by February 23, 2015, we will hold a public hearing on March 4,
2015. If you are interested in requesting a public hearing or attending
the public hearing, contact Ms. Pamela Garrett at (919) 541-7966 or at
garrett.pamela@epa.gov. If the EPA holds a public hearing, the EPA will
keep the record of the hearing open for 30 days after completion of the
hearing to provide an opportunity for submission of rebuttal and
supplementary information.
ADDRESSES: Comments. Submit your comments, identified by Docket ID No.
EPA-HQ-OAR-2014-0830, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the online instructions for submitting comments.
Email: A-and-R-Docket@epa.gov. Include Attention Docket ID
No. EPA-HQ-OAR-2014-0830 in the subject line of the message.
Fax: (202) 566-9744, Attention Docket ID No. EPA-HQ-OAR-
2014-0830.
Mail: Environmental Protection Agency, EPA Docket Center
(EPA/DC), Mail Code 28221T, Attention Docket ID No. EPA-HQ-OAR-2014-
0830, 1200 Pennsylvania Avenue 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
Street NW., Washington, DC 20503.
Hand/Courier Delivery: EPA Docket Center, Room 3334, EPA
WJC West Building, 1301 Constitution Avenue NW., Washington, DC 20004,
Attention Docket ID No. EPA-HQ-OAR-2014-0830. 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-
2014-0830. The EPA's policy is that all comments received will be
included in the public docket without change and may be made available
online at https://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 https://www.regulations.gov or email. The https://www.regulations.gov Web site
is an ``anonymous access'' system, which means the EPA will not know
your identity or contact information unless you provide it in the body
of your comment. If you send an email comment directly to the EPA
without going through https://www.regulations.gov, your email 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, the 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 the EPA cannot read your comment
due to technical difficulties and cannot contact you for clarification,
the EPA may not be able to consider your comment. Electronic files
should not include special characters or any form of encryption and be
free of any defects or viruses. For additional information about the
EPA's public docket, visit the EPA Docket Center homepage at: https://www.epa.gov/dockets.
Docket. The EPA has established a docket for this rulemaking under
Docket ID No. EPA-HQ-OAR-2014-0830. All documents in the docket are
listed in the https://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, is not placed on the Internet
and will be publicly available only in hard copy. Publicly available
docket materials are available either electronically in regulations.gov
or in hard copy at the EPA Docket Center, Room 3334, EPA WJC West
Building, 1301 Constitution Avenue 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 EPA
Docket Center is (202) 566-1742.
Public Hearing. If a public hearing is requested by February 23,
2015, it will be held on March 4, 2015 at the EPA's Research Triangle
Park Campus, 109 T.W. Alexander Drive, Research Triangle Park, NC
27711. The hearing will convene at 10:00 a.m. (Eastern Standard Time)
and end at 5:00 p.m. (Eastern Standard Time). A lunch break will be
held from 12:00 p.m. (Eastern Standard Time) until 1:00 p.m. (Eastern
Standard Time). Please contact Ms. Pamela Garrett at (919) 541-7966 or
at garrett.pamela@epa.gov to request a hearing, to determine if a
hearing will be held and to register to speak at the hearing, if one is
held. If a hearing is requested, the last day to pre-register in
advance to speak at the hearing will be March 2, 2015.
Additionally, requests to speak will be taken the day of the
hearing at the hearing registration desk, although preferences on
speaking times may not be able to be fulfilled. If you require the
service of a translator or special accommodations such as audio
description, please let us know at the time of registration. If you
require an accommodation, we ask that you preregister for the hearing,
as we may not be able to arrange such
[[Page 8393]]
accommodations without advance notice.
If no one contacts the EPA requesting a public hearing to be held
concerning this proposed rule by February 23, 2015, a public hearing
will not take place. If a hearing is held, it will provide interested
parties the opportunity to present data, views or arguments concerning
the proposed action. The EPA will make every effort to accommodate all
speakers who arrive and register. Because the hearing will be held at a
U.S. governmental facility, individuals planning to attend the hearing
should be prepared to show valid picture identification to the security
staff in order to gain access to the meeting room. Please note that the
REAL ID Act, passed by Congress in 2005, established new requirements
for entering federal facilities. If your driver's license is issued by
Alaska, American Samoa, Arizona, Kentucky, Louisiana, Maine,
Massachusetts, Minnesota, Montana, New York, Oklahoma or the state of
Washington, you must present an additional form of identification to
enter the federal building. Acceptable alternative forms of
identification include: federal employee badges, passports, enhanced
driver's licenses and military identification cards. In addition, you
will need to obtain a property pass for any personal belongings you
bring with you. Upon leaving the building, you will be required to
return this property pass to the security desk. No large signs will be
allowed in the building, cameras may only be used outside of the
building and demonstrations will not be allowed on federal property for
security reasons.
The EPA may ask clarifying questions during the oral presentations,
but will not respond to the presentations at that time. Written
statements and supporting information submitted during the comment
period will be considered with the same weight as oral comments and
supporting information presented at the public hearing. Commenters
should notify Ms. Garrett if they will need specific equipment, or if
there are other special needs related to providing comments at the
hearing. Verbatim transcripts of the hearings and written statements
will be included in the docket for the rulemaking. The EPA will make
every effort to follow the schedule as closely as possible on the day
of the hearing; however, please plan for the hearing to run either
ahead of schedule or behind schedule. Again, a hearing will not be held
unless requested.
FOR FURTHER INFORMATION CONTACT: For questions about this proposed
action, contact Kim Teal, Sector Policies and Programs Division (D243-
02), Office of Air Quality Planning and Standards, U.S. Environmental
Protection Agency, Research Triangle Park, North Carolina 27711;
telephone number: (919) 541-5580; fax number: (919) 541-5450; and email
address: teal.kim@epa.gov. For specific information regarding the risk
modeling methodology, contact Ted Palma, Health and Environmental
Impacts Division (C539-02), Office of Air Quality Planning and
Standards, U.S. Environmental Protection Agency, Research Triangle
Park, North Carolina 27711; telephone number: (919) 541-5470; fax
number: (919) 541-0840; and email address: palma.ted@epa.gov. For
information about the applicability of the NESHAP to a particular
entity, contact Rafael Sanchez, Office of Enforcement and Compliance
Assurance (OECA), (202) 564-7028, sanchez.rafael@epa.gov.
SUPPLEMENTARY INFORMATION:
Preamble Acronyms and Abbreviations. We use multiple acronyms and
terms in this preamble. While this list may not be exhaustive, to ease
the reading of this preamble and for reference purposes, the EPA
defines the following terms and acronyms here:
AD Airworthiness Directive
AEGL acute exposure guideline level
AERMOD air dispersion model used by the HEM-3 model
ATSDR Agency for Toxic Substances and Disease Registry
BACT Best Achievable Control Technology
CAA Clean Air Act
CalEPA California EPA
CBI Confidential Business Information
CDX EPA's Central Data Exchange
CEDRI EPA's Compliance and Emissions Data Reporting Interface
CFR Code of Federal Regulations
CTG Control Technique Guideline document
EJ environmental justice
EPA Environmental Protection Agency
ERPG Emergency Response Planning Guidelines
ERT EPA's Electronic Reporting Tool
FAA Federal Aviation Administration
FR Federal Register
g/L grams/liter
HAP hazardous air pollutants
HCl hydrochloric acid
HEM-3 Human Exposure Model, Version 1.1.0
HF hydrogen fluoride
HI hazard index
HQ hazard quotient
HVLP high volume low pressure
IARC International Agency for Research on Cancer
ICR information collection request
IRIS Integrated Risk Information System
km kilometer
lb/gal pounds/gallon
LOAEL Lowest-observed-adverse-effect level
MACT maximum achievable control technology
mg/m\3\ milligrams per cubic meter
MIR maximum individual risk
mm Hg millimeters mercury
NAAQS National Ambient Air Quality Standards
NAICS North American Industry Classification System
NAS National Academy of Sciences
NATA National Air Toxics Assessment
NEI National Emission Inventory
NESHAP National Emissions Standards for Hazardous Air Pollutants
NOAA National Oceanic and Atmospheric Administration
NOAEL No-observed-adverse-effect levels
NRC National Research Council
NRDC Natural Resources Defense Council
NTP National Toxicology Program
NTTAA National Technology Transfer and Advancement Act
OAQPS Office of Air Quality Planning and Standards
OECA Office of Enforcement and Compliance Assurance
OEM original equipment manufacturer
OMB Office of Management and Budget
PAH polycyclic aromatic hydrocarbons
PB-HAP hazardous air pollutants known to be persistent and bio-
accumulative in the environment
PEL Probable effect level
POM polycyclic organic matter
ppm parts per million
PSD Prevention of Significant Deterioration
RACT Reasonably Available Control Technology
RBLC EPA's RACT/BACT/LAER Clearinghouse
RCRA Resource Conservation and Recovery Act of 1976
REL reference exposure level
RFA Regulatory Flexibility Act
RfC reference concentration
RfD reference dose
RoC Report of the Carcinogens
RTR residual risk and technology review
SAB Science Advisory Board
SCAQMD South Coast Air Quality Management District
SSM startup, shutdown and malfunction
TOSHI target organ-specific hazard index
tpy tons per year
TRIM.FaTE Total Risk Integrated Methodology.Fate, Transport, and
Ecological Exposure model
TTN Technology Transfer Network
UF uncertainty factor
[mu]g/m\3\ microgram per cubic meter
UMRA Unfunded Mandates Reform Act
URE unit risk estimate
VOC volatile organic compounds
Organization of this Document. The information in this preamble is
organized as follows:
I. General Information
A. Does this action apply to me?
B. Where can I get a copy of this document and other related
information?
C. What should I consider as I prepare my comments for the EPA?
II. Background
A. What is the statutory authority for this action?
[[Page 8394]]
B. What is this source category and how does the current NESHAP
regulate its HAP emissions?
C. What data collection activities were conducted to support
this action?
D. What other relevant background information and data are
available?
E. What litigation is related to this proposed action?
III. Analytical Procedures
A. How did we estimate post-MACT risks posed by the source
category?
B. How did we consider the risk results in making decisions for
this proposal?
C. How did we perform the technology review?
IV. Analytical Results and Proposed Decisions
A. What actions are we taking pursuant to CAA sections 112(d)(2)
and 112(d)(3)?
B. What are the results of the risk assessment and analyses?
C. What are our proposed decisions regarding risk acceptability,
ample margin of safety and adverse environmental effects?
D. What are the results and proposed decisions based on our
technology review?
E. What other actions are we proposing?
F. What compliance dates are we proposing?
V. Summary of Cost, Environmental and Economic Impacts
A. What are the affected sources?
B. What are the air quality impacts?
C. What are the cost impacts?
D. What are the economic impacts?
E. What are the benefits?
VI. Request for Comments
VII. Submitting Data Corrections
VIII. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory Planning and Review and
Executive Order 13563: Improving Regulation and Regulatory Review
B. Paperwork Reduction Act
C. Regulatory Flexibility Act (RFA)
D. Unfunded Mandates Reform Act (UMRA)
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 Risks and Safety Risks
H. Executive Order 13211: Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution or Use
I. National Technology Transfer and Advancement Act (NTTAA)
J. Executive Order 12898: Federal Actions to Address
Environmental Justice in Minority Populations and Low-Income
Populations
I. General Information
A. Does this action apply to me?
Table 1 of this preamble lists the regulated industrial source
category that is the subject of this proposal. Table 1 is not intended
to be exhaustive, but rather to provide a guide for readers regarding
the entities that this proposed action is likely to affect. The
proposed standards, once promulgated, will be directly applicable to
the affected sources. Federal government entities may be affected by
this proposed action. Parties potentially affected by this action
include major and synthetic minor source installations that are owned
or operated by the Armed Forces of the United States (including the
Department of Defense and the Coast Guard) and the National Aeronautics
and Space Administration. As defined under the ``Surface Coating''
industry sector in the ``Initial List of Categories of Sources Under
Section 112(c)(1) of the Clean Air Act Amendments of 1990'' (see 57 FR
31576, July 16, 1992), the Aerospace Manufacturing and Rework
Facilities source category is any facility engaged, either in part or
in whole, in the manufacture or rework of commercial, civil or military
aerospace vehicles or components and that are major sources as defined
in 40 CFR 63.2.
Table 1--Industrial Source Category Affected by This Proposed Action
------------------------------------------------------------------------
Source Category NESHAP NAICS code \a\
------------------------------------------------------------------------
Aerospace Manufacturing and Aerospace 336411, 336412,
Rework Facilities. Manufacturing and 336413, 336414,
Rework Facilities. 336415, 336419,
481111, 481112,
481211, 481212,
481219.
------------------------------------------------------------------------
\a\ North American Industry Classification System.
B. Where can I get a copy of this document and other related
information?
In addition to being available in the docket, an electronic copy of
this action is available on the Internet through the EPA's Technology
Transfer Network (TTN) Web site, a forum for information and technology
exchange in various areas of air pollution control. Following signature
by the EPA Administrator, the EPA will post a copy of this proposed
action at: https://www.epa.gov/ttn/atw/aerosp/aeropg.html. Following
publication in the Federal Register, the EPA will post the Federal
Register version of the proposal and key technical documents at this
same Web site. Information on the overall residual risk and technology
review program is available at the following Web site: https://www.epa.gov/ttn/atw/rrisk/rtrpg.html.
C. What should I consider as I prepare my comments for the EPA?
Submitting CBI. Do not submit information containing CBI to the EPA
through https://www.regulations.gov or email. Clearly mark the part or
all of the information that you claim to be CBI. For CBI information on
a disk or CD-ROM that you mail to the 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 comments that includes information claimed
as CBI, you must submit a copy of the comments that does not contain
the information claimed as CBI for inclusion in the public docket. If
you submit a CD-ROM or disk that does not contain CBI, 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 and the EPA's
electronic public docket without prior notice. Information marked as
CBI will not be disclosed except in accordance with procedures set
forth in 40 Code of Federal Regulations (CFR) part 2. Send or deliver
information identified as CBI only to the following address: OAQPS
Document Control Officer (C404-02), OAQPS, U.S. Environmental
Protection Agency, Research Triangle Park, North Carolina 27711,
Attention Docket ID No. EPA-HQ-OAR-2014-0830.
II. Background
A. What is the statutory authority for this action?
Section 112 of the CAA establishes a two-stage regulatory process
to address emissions of HAP from stationary sources. In the first
stage, after the EPA has identified categories of sources emitting one
or more of the HAP listed in CAA section 112(b), CAA section 112(d)
requires us to promulgate technology-based NESHAP for those
[[Page 8395]]
sources. ``Major sources'' are those that emit or have the potential to
emit 10 tons per year (tpy) or more of a single HAP or 25 tpy or more
of any combination of HAP. For major sources, the technology-based
NESHAP must reflect the maximum degree of emission reductions of HAP
achievable (after considering cost, energy requirements and non-air
quality health and environmental impacts) and are commonly referred to
as maximum achievable control technology (MACT) standards.
MACT standards must reflect the maximum degree of emissions
reduction achievable through the application of measures, processes,
methods, systems or techniques, including, but not limited to, measures
that: (1) Reduce the volume of or eliminate pollutants through process
changes, substitution of materials or other modifications; (2) enclose
systems or processes to eliminate emissions; (3) capture or treat
pollutants when released from a process, stack, storage or fugitive
emissions point; (4) are design, equipment, work practice or
operational standards (including requirements for operator training or
certification); or (5) are a combination of the above. CAA section
112(d)(2)(A) through (E). The MACT standards may take the form of
design, equipment, work practice or operational standards where the EPA
first determines either that: (1) A pollutant cannot be emitted through
a conveyance designed and constructed to emit or capture the pollutant,
or that any requirement for or use of, such a conveyance would be
inconsistent with law; or (2) the application of measurement
methodology to a particular class of sources is not practicable due to
technological and economic limitations. CAA section 112(h)(1) and (2).
The MACT ``floor'' is the minimum control level allowed for MACT
standards promulgated under CAA section 112(d)(3) and may not be based
on cost considerations. For new sources, the MACT floor cannot be less
stringent than the emissions control that is achieved in practice by
the best-controlled similar source. The MACT floor for existing sources
can be less stringent than floors for new sources, but not less
stringent than the average emissions limitation achieved by the best-
performing 12 percent of existing sources in the category or
subcategory (or the best-performing five sources for categories or
subcategories with fewer than 30 sources). In developing MACT
standards, the EPA must also consider control options that are more
stringent than the floor. We may establish standards more stringent
than the floor based on considerations of the cost of achieving the
emission reductions, any non-air quality health and environmental
impacts and energy requirements.
The EPA is then required to review these technology-based standards
and revise them ``as necessary (taking into account developments in
practices, processes and control technologies)'' no less frequently
than every 8 years. CAA section 112(d)(6). In conducting this review,
the EPA is not required to recalculate the MACT floor. Natural
Resources Defense Council (NRDC) v. EPA, 529 F.3d 1077, 1084 (D.C. Cir.
2008). Association of Battery Recyclers, Inc. v. EPA, 716 F.3d 667
(D.C. Cir. 2013).
The second stage in standard-setting focuses on reducing any
remaining (i.e., ``residual'') risk according to CAA section 112(f).
CAA Section 112(f)(1) required that the EPA prepare a report to
Congress discussing (among other things) methods of calculating the
risks posed (or potentially posed) by sources after implementation of
the MACT standards, the public health significance of those risks and
the EPA's recommendations as to legislation regarding such remaining
risk. The EPA prepared and submitted the Residual Risk Report to
Congress, EPA-453/R-99-001 (Risk Report) in March 1999. CAA section
112(f)(2) then provides that if Congress does not act on any
recommendation in the Risk Report, the EPA must analyze and address
residual risk for each category or subcategory of sources 8 years after
promulgation of such standards pursuant to CAA section 112(d).
Section 112(f)(2) of the CAA requires the EPA to determine for
source categories subject to MACT standards whether the emission
standards provide an ample margin of safety to protect public health.
Section 112(f)(2)(B) of the CAA expressly preserves the EPA's use of
the two-step process for developing standards to address any residual
risk and the agency's interpretation of ``ample margin of safety''
developed in the National Emissions Standards for Hazardous Air
Pollutants: Benzene Emissions from Maleic Anhydride Plants,
Ethylbenzene/Styrene Plants, Benzene Storage Vessels, Benzene Equipment
Leaks, and Coke By-Product Recovery Plants (Benzene NESHAP) (54 FR
38044, September 14, 1989). The EPA notified Congress in the Risk
Report that the agency intended to use the Benzene NESHAP approach in
making CAA section 112(f) residual risk determinations (EPA-453/R-99-
001, p. ES-11). The EPA subsequently adopted this approach in its
residual risk determinations and in a challenge to the risk review for
the Synthetic Organic Chemical Manufacturing source category, the
United States Court of Appeals for the District of Columbia Circuit
upheld as reasonable the EPA's interpretation that subsection 112(f)(2)
incorporates the approach established in the Benzene NESHAP. See NRDC
v. EPA, 529 F.3d 1077, 1083 (D.C. Cir. 2008) (``[S]ubsection
112(f)(2)(B) expressly incorporates the EPA's interpretation of the
Clean Air Act from the Benzene standard, complete with a citation to
the Federal Register.''); see also A Legislative History of the Clean
Air Act Amendments of 1990, vol. 1, p. 877 (Senate debate on Conference
Report).
The first step in the process of evaluating residual risk is the
determination of acceptable risk. If risks are unacceptable, the EPA
cannot consider cost in identifying the emissions standards necessary
to bring risks to an acceptable level. The second step is the
determination of whether standards must be further revised in order to
provide an ample margin of safety to protect public health. The ample
margin of safety is the level at which the standards must be set,
unless an even more stringent standard is necessary to prevent, taking
into consideration costs, energy, safety and other relevant factors, an
adverse environmental effect.
1. Step 1--Determination of Acceptability
The agency in the Benzene NESHAP concluded that ``the acceptability
of risk under section 112 is best judged on the basis of a broad set of
health risk measures and information'' and that the ``judgment on
acceptability cannot be reduced to any single factor.'' Benzene NESHAP
at 38046. The determination of what represents an ``acceptable'' risk
is based on a judgment of ``what risks are acceptable in the world in
which we live'' (Risk Report at 178, quoting NRDC v. EPA, 824 F. 2d
1146, 1165 (D.C. Cir. 1987) (en banc) (``Vinyl Chloride''), recognizing
that our world is not risk-free.
In the Benzene NESHAP, we stated that ``EPA will generally presume
that if the risk to [the maximum exposed] individual is no higher than
approximately one in 10 thousand, that risk level is considered
acceptable.'' 54 FR 38045, September 14, 1989. We discussed the maximum
individual lifetime cancer risk (or maximum individual risk (MIR)) as
being ``the estimated risk that a person living near a plant would have
if he or she were
[[Page 8396]]
exposed to the maximum pollutant concentrations for 70 years.'' Id. We
explained that this measure of risk ``is an estimate of the upper bound
of risk based on conservative assumptions, such as continuous exposure
for 24 hours per day for 70 years.'' Id. We acknowledged that maximum
individual lifetime cancer risk ``does not necessarily reflect the true
risk, but displays a conservative risk level which is an upper-bound
that is unlikely to be exceeded.'' Id.
Understanding that there are both benefits and limitations to using
the MIR as a metric for determining acceptability, we acknowledged in
the Benzene NESHAP that ``consideration of maximum individual risk * *
* must take into account the strengths and weaknesses of this measure
of risk.'' Id. Consequently, the presumptive risk level of 100-in-1
million (1-in-10 thousand) provides a benchmark for judging the
acceptability of maximum individual lifetime cancer risk, but does not
constitute a rigid line for making that determination. Further, in the
Benzene NESHAP, we noted that:
[p]articular attention will also be accorded to the weight of
evidence presented in the risk assessment of potential
carcinogenicity or other health effects of a pollutant. While the
same numerical risk may be estimated for an exposure to a pollutant
judged to be a known human carcinogen, and to a pollutant considered
a possible human carcinogen based on limited animal test data, the
same weight cannot be accorded to both estimates. In considering the
potential public health effects of the two pollutants, the Agency's
judgment on acceptability, including the MIR, will be influenced by
the greater weight of evidence for the known human carcinogen.
Id. at 38046. The agency also explained in the Benzene NESHAP that:
[i]n establishing a presumption for MIR, rather than a rigid line
for acceptability, the Agency intends to weigh it with a series of
other health measures and factors. These include the overall
incidence of cancer or other serious health effects within the
exposed population, the numbers of persons exposed within each
individual lifetime risk range and associated incidence within,
typically, a 50 km exposure radius around facilities, the science
policy assumptions and estimation uncertainties associated with the
risk measures, weight of the scientific evidence for human health
effects, other quantified or unquantified health effects, effects
due to co-location of facilities, and co-emission of pollutants.
Id. at 38045. In some cases, these health measures and factors
taken together may provide a more realistic description of the
magnitude of risk in the exposed population than that provided by
maximum individual lifetime cancer risk alone.
As noted earlier, in NRDC v. EPA, the court held that CAA section
112(f)(2) ``incorporates the EPA's interpretation of the Clean Air Act
from the Benzene Standard.'' The court further held that Congress'
incorporation of the Benzene standard applies equally to carcinogens
and non-carcinogens. 529 F.3d at 1081-82. Accordingly, we also consider
non-cancer risk metrics in our determination of risk acceptability and
ample margin of safety.
2. Step 2--Determination of Ample Margin of Safety
CAA section 112(f)(2) requires the EPA to determine, for source
categories subject to MACT standards, whether those standards provide
an ample margin of safety to protect public health. As explained in the
Benzene NESHAP, ``the second step of the inquiry, determining an `ample
margin of safety,' again includes consideration of all of the health
factors, and whether to reduce the risks even further . . . Beyond that
information, additional factors relating to the appropriate level of
control will also be considered, including costs and economic impacts
of controls, technological feasibility, uncertainties and any other
relevant factors. Considering all of these factors, the agency will
establish the standard at a level that provides an ample margin of
safety to protect the public health, as required by section 112.'' 54
FR 38046, September 14, 1989.
According to CAA section 112(f)(2)(A), if the MACT standards for
HAP ``classified as a known, probable, or possible human carcinogen do
not reduce lifetime excess cancer risks to the individual most exposed
to emissions from a source in the category or subcategory to less than
one in one million,'' the EPA must promulgate residual risk standards
for the source category (or subcategory), as necessary to provide an
ample margin of safety to protect public health. In doing so, the EPA
may adopt standards equal to existing MACT standards if the EPA
determines that the existing standards (i.e., the MACT standards) are
sufficiently protective. NRDC v. EPA, 529 F.3d 1077, 1083 (D.C. Cir.
2008) (``If EPA determines that the existing technology-based standards
provide an `ample margin of safety,' then the Agency is free to readopt
those standards during the residual risk rulemaking.'') The EPA must
also adopt more stringent standards, if necessary, to prevent an
adverse environmental effect,\1\ but must consider cost, energy, safety
and other relevant factors in doing so.
---------------------------------------------------------------------------
\1\ ``Adverse environmental effect'' is defined as any
significant and widespread adverse effect, which may be reasonably
anticipated to wildlife, aquatic life or natural resources,
including adverse impacts on populations of endangered or threatened
species or significant degradation of environmental qualities over
broad areas. See CAA section 112(a)(7).
---------------------------------------------------------------------------
The CAA does not specifically define the terms ``individual most
exposed,'' ``acceptable level'' and ``ample margin of safety.'' In the
Benzene NESHAP, 54 FR 38044-38045, September 14, 1989, we stated as an
overall objective:
In protecting public health with an ample margin of safety under
section 112, EPA strives to provide maximum feasible protection
against risks to health from hazardous air pollutants by (1)
protecting the greatest number of persons possible to an individual
lifetime risk level no higher than approximately 1-in-1 million and
(2) limiting to no higher than approximately 1-in-10 thousand [i.e.,
100-in-1 million] the estimated risk that a person living near a
plant would have if he or she were exposed to the maximum pollutant
concentrations for 70 years.
The agency further stated that ``[t]he EPA also considers incidence
(the number of persons estimated to suffer cancer or other serious
health effects as a result of exposure to a pollutant) to be an
important measure of the health risk to the exposed population.
Incidence measures the extent of health risks to the exposed population
as a whole, by providing an estimate of the occurrence of cancer or
other serious health effects in the exposed population.'' Id. at 38045.
In the ample margin of safety decision process, the agency again
considers all of the health risks and other health information
considered in the first step, including the incremental risk reduction
associated with standards more stringent than the MACT standard or a
more stringent standard that EPA has determined is necessary to ensure
risk is acceptable. In the ample margin of safety analysis, the agency
considers additional factors, including costs and economic impacts of
controls, technological feasibility, uncertainties and any other
relevant factors. Considering all of these factors, the agency will
establish the standard at a level that provides an ample margin of
safety to protect the public health, as required by CAA section 112(f).
54 FR 38046, September 14, 1989.
[[Page 8397]]
B. What is this source category and how does the current NESHAP
regulate its HAP emissions?
1. Description of the Aerospace Manufacturing and Rework Facilities
Source Category and Applicability.
The NESHAP for the Aerospace Manufacturing and Rework Facilities
source category (henceforth referred to as the ``Aerospace NESHAP'')
was promulgated on September 1, 1995 (60 FR 45956) and codified at 40
CFR part 63, subpart GG. As promulgated in 1995, the Aerospace NESHAP
applies to the surface coating and related operations at each new and
existing affected source of HAP emissions at facilities that are major
sources and are engaged, either in part or in whole, in the manufacture
or rework of commercial, civil or military aerospace vehicles or
components. The requirements of the standards are nearly the same for
both new and existing sources. The Aerospace NESHAP (40 CFR 63.742)
defines ``aerospace vehicle or component'' as ``any fabricated part,
processed part, assembly of parts or completed unit, with the exception
of electronic components, of any aircraft, including, but not limited
to airplanes, helicopters, missiles, rockets, and space vehicles.''
Today, we estimate that 144 facilities are subject to the Aerospace
NESHAP. A complete list of facilities subject to the Aerospace NESHAP
is available in the Aerospace RTR database, which is available for
review in the docket for this proposed rulemaking. Section 63.741(c)
defines each affected source in the Aerospace Manufacturing and Rework
Facilities source category, and a facility could have a combination of
both new and existing affected sources. However, the emission standards
for new and existing affected sources are the same for nearly all
operations within subpart GG. The exceptions are the filter efficiency
requirements to control inorganic HAP emissions from primer and topcoat
spray application operations in 40 CFR 63.745 and for dry media
blasting operations in 40 CFR 63.746 and the requirements for controls
to reduce organic HAP emissions from chemical depainting operations in
40 CFR 63.746(c).
The Aerospace NESHAP applies to organic HAP emissions from cleaning
operations, depainting operations, primer application operations,
topcoat application operations, chemical milling maskant application
operations and the handling and storage of waste. The rule also applies
to inorganic HAP emissions from primer and topcoat application
operations using spray equipment and depainting operations using dry
media blasting. The rule provides an exemption for primers, topcoats
and chemical milling maskants used in low-volumes which is defined as
189 liters (50 gallons) or less per formulation and for which the
combined annual total does not exceed 757 liters (200 gallons).
The current Aerospace NESHAP explicitly excludes specialty coatings
from meeting any control requirements, as specified in 40 CFR 63.741(f)
and in 40 CFR 63.742 (i.e., the definitions for ``exterior primer,''
``primer,'' and ``topcoat''). Appendix A of the Aerospace NESHAP
defines 59 separate categories of specialty coatings.
Although the EPA did not include emission limitations for specialty
coatings in the Aerospace NESHAP finalized in 1995 or in any subsequent
amendments, the EPA included VOC content limits for the 59 categories
of specialty coatings in the 1997 Aerospace Control Techniques
Guidelines (CTG) document.\2\ The CAA requires that state
implementation plans (SIPs) for certain ozone nonattainment areas be
revised to require the implementation of reasonably available control
technology (RACT) to control volatile organic compounds (VOC)
emissions. The EPA has defined RACT as the lowest emission limitation
that a particular source is capable of meeting by the application of
control technology that is reasonably available considering
technological and economic feasibility. The Aerospace CTG is intended
to provide state and local air pollution control authorities with an
information base, recommended emissions limitations and monitoring,
recordkeeping and reporting requirements for proceeding with their
analyses of reasonably available control technology (RACT) for their
own regulations to reduce VOC emissions from aerospace surface coating
operations.
---------------------------------------------------------------------------
\2\ Guideline Series: Control of Volatile Organic Compound
Emissions from Coating Operations at Aerospace Manufacturing and
Rework Operations. Emission Standards Division, U. S. Environmental
Protection Agency, Office of Air and Radiation, Office of Air
Quality Planning and Standards, Research Triangle Park, NC 27711,
December 1997. Publication No. EPA-453/R-97-004.
---------------------------------------------------------------------------
2. Organic and Inorganic HAP Emission Sources
Organic HAP emissions from cleaning and depainting operations occur
from the evaporation of the volatile portion of the cleaning solvents
or chemical strippers. Cleaning emissions are typically fugitive in
nature and occur at most processing steps. Emissions from depainting
operations that occur within a booth or hangar are typically captured
and exhausted through a stack, although some emissions may be fugitive
in nature (e.g., open tanks).
Organic HAP emissions from coating (primers, topcoats and chemical
milling maskants) application operations occur from the evaporation of
the solvent contained in the coatings. These emissions occur during the
application of the coatings on aerospace vehicles or parts, which may
take place in large open areas, such as hangars or in partially or
fully enclosed spaces, such as within spray booths.
Organic HAP emissions from waste occur from evaporation of the
volatile portion of the waste while it is being handled or stored.
These emissions are fugitive in nature, occurring from each waste
container.
Some coatings contain compounds that are inorganic HAP. Inorganic
HAP emissions from coatings occur during the application of the coating
if it is applied using spray guns. These inorganic HAP emissions are
paint particulates, commonly referred to as ``overspray,'' that do not
adhere to the surface being coated. Like the organic HAP emissions from
the operations, the emissions of the inorganic HAP may occur in large
open areas, such as hangars or in partially or fully enclosed spaces,
such as within spray booths. However, coatings that contain inorganic
HAP are typically applied in spray booths equipped with exhaust filters
to capture paint overspray. Inorganic HAP are not emitted from coatings
applied with non-spray methods, such as brushes, rollers or dip
coating, because the coating is not atomized with these methods.
Inorganic HAP emissions from depainting operations may occur from
non-chemical methods, such as plastic and other types of dry media
blasting, used to strip an aerospace vehicle. (Chemical stripping
techniques do not release inorganic HAP.) These emissions occur as
particulates generated during the blasting process. The operation is
typically carried out within a large hangar equipped with a ventilation
system and particulate filtration device (e.g., a baghouse) or in
smaller enclosures, also equipped with filtration. The inorganic HAP
that are released from the depainting operations are primarily found in
the paint being stripped, although some stripping media may contain
trace amounts of inorganic HAP.
[[Page 8398]]
3. Regulation of Organic and Inorganic HAP Emissions in the Aerospace
NESHAP
The Aerospace NESHAP specifies numerical emission limits for
organic HAP emissions from primer, topcoat, chemical milling maskant
application operations and chemical depainting operations; equipment
and filter efficiency requirements for dry media blasting depainting
operations and spray applied coating operations; composition
requirements and equipment standards for cleaning operations; and work
practice standards for waste handling and storage operations.
The organic HAP emission rate for primers is 540 grams/liter (g/L)
(4.5 pounds/gallon (lb/gal)) (less water) for general aviation rework
facilities; 650 g/L (5.4 lb/gal) (less water) for large commercial
aircraft; or 350 g/L (2.9 lb/gal) for other primers (40 CFR
63.745(c)(1) and (2)). For topcoats and self-priming topcoats the
emission rate is 420 g/L (3.5 lb/gal) (less water); and 540 g/L (4.5
lb/gal) (less water) for primers and self-priming topcoats at general
aviation rework facilities (40 CFR 63.745(c)(3) and (4)).
Alternatively, a control system can be used to capture and control
emissions from the primer or topcoat application operation (40 CFR
63.745(d)). The system must achieve an overall control efficiency of 81
percent. Further, the Aerospace NESHAP specifies which types of coating
application techniques may be used (40 CFR 63.745(f)). The Aerospace
NESHAP also provides operating requirements for the application of
primers or topcoats that contain inorganic HAP, including control of
spray booth exhaust streams with either particulate filters or
waterwash systems (40 CFR 63.745(g)). The primer and topcoat limits and
control requirements do not apply to specialty coatings defined in
Appendix A to subpart GG.
The organic HAP emission content limits for chemical milling
maskants for use with Type I chemical milling solutions is 622 g/L (5.2
lb/gal) (less water) and 160 g/L (1.3 lb/gal) (less water) for use with
Type II chemical milling solutions (40 CFR 63.747(c)). Alternatively, a
control system that achieves an overall control efficiency of 81
percent can be used to capture and control emissions from the maskant
application operation (40 CFR 63.747(d)). These requirements do not
apply to touch-up of scratched surfaces or damaged maskant and touch-up
of trimmed edges.
For cleaning operations (including hand-wipe cleaning), the
Aerospace NESHAP specifies that cleaning solvents meet certain
composition requirements or that the cleaning solvents have a composite
vapor pressure of no more than 45 millimeters mercury (mm Hg) (24.1 in.
water) (40 CFR 63.744(b)). Work practice measures are also required (40
CFR 63.744(a)). Four work practice alternative techniques are specified
for spray gun cleaning, and work practice standards are specified for
flush cleaning operations (40 CFR 63.744(c) and (d)).
The Aerospace NESHAP also specifies requirements for depainting
operations. Where there are no controls for organic HAP emissions from
chemical depainting operations, the rule prohibits organic HAP
emissions from chemical depainting operations, with the exception that
26 gallons of HAP-containing chemical stripper (or alternatively 190
pounds of organic HAP) may be used for each commercial aircraft
stripped, or 50 gallons (or 365 pounds of organic HAP) for each
military aircraft for spot stripping and decal removal (40 CFR
63.746(b)(1) through (3)). Where there are controls for organic HAP
emissions from chemical depainting, emissions must be reduced by 81
percent for controls installed before the effective date, and by 95
percent for controls installed on or after the effective date (40 CFR
63.746(c)). For non-chemical depainting operations that generate
inorganic HAP emissions from dry media blasting, the operation must be
performed in an enclosed area or in a closed cycle depainting system
and the air stream from the operation must pass through a dry filter
system meeting a minimum efficiency specified in the rule, through a
baghouse or through a waterwash system before being released to the
atmosphere (40 CFR 63.746(b)(4)).
The handling and storage of waste that contains HAP must be
conducted in a manner that minimizes spills (40 CFR 63.748).
C. What data collection activities were conducted to support this
action?
In February 2011, the EPA issued an information collection request
(ICR), pursuant to CAA section 114, to approximately 1,300 facilities
that were thought to potentially own and operate Aerospace
Manufacturing and Rework Facilities. Information was requested on
operations subject to the Aerospace NESHAP (coatings, blast depainting
operations, solvent depainting operations and solvent cleaning
operations) as well as specialty coatings, chemical milling and metal
finishing operations, composite processing, storage tanks and
wastewater treatment. Information was also requested on booth
characteristics and control devices and location coordinates (latitude
and longitude) of emission stacks and operations. The ICR requested
available information regarding coating and solvent usage, process
equipment, control devices used, point and fugitive HAP emissions,
practices used to control HAP emissions and other aspects of facility
operations. A total of 87 major source facilities and 57 synthetic
minor facilities responded to the survey and were included in the risk
modeling analysis. The remaining facilities were either area source
facilities, not aerospace manufacturing or rework facilities or closed
facilities, or the ICR was returned undeliverable. We received data on
coating and solvent usage, chemical milling, metal finishing,
depainting operations, composite processing operations, storage tanks,
wastewater treatment operations and use of add-on control devices. From
these data, we were able to calculate HAP emissions for each of the
major source and synthetic minor facilities that responded to the
survey.
In October 2012, the EPA issued a request for stack test data under
the authority of section 114 of the CAA. This request was sent to 9
parent companies for 18 facilities, requesting stack emissions testing
data for selected coating operations and spray booths and blast
depainting, composite processing and metal finishing operations
believed to represent the various processes and capture and control
configurations used by the industry. All facilities either responded to
the survey or provided information indicating the operations for which
we requested stack testing had been shutdown.
In September 2013, the EPA issued an additional request to the same
companies requesting supplemental testing to confirm the content of the
coatings used in the October 2012 stack testing. These data were used
to speciate emissions for individual coatings and to develop the
default chromium speciation profile for processes included in the 2011
ICR.
In May 2014, the EPA solicited industry review of the EPA's draft
modeling file records (e.g., estimated emissions and emission
estimation methods) that were developed based on the results of the
data collection efforts described above and the 2011 National Emission
Inventory (NEI) and 2005 National Air Toxics Assessment (NATA)
discussed in section II.D of this preamble. Of the 171 facilities
contacted, 84 facilities responded. Of the 171 facilities contacted,
the EPA determined that 144 are in operation
[[Page 8399]]
and subject to the NESHAP and 27 facilities are closed or not subject
to the Aerospace NESHAP (e.g., are area sources). The 144 facilities
that were determined to be in operation and subject to the NESHAP are
included in the model input file for the risk assessment.
D. What other relevant background information and data are available?
The 2011 NEI provided supplemental information for this RTR. The
NEI is a database that contains information about sources that emit
criteria air pollutants, their precursors and HAP. The database
includes estimates of annual air pollutant emissions from point,
nonpoint and mobile sources in the 50 states, the District of Columbia,
Puerto Rico and the Virgin Islands. The EPA collects this information
and releases an updated version of the NEI database every 3 years. The
NEI includes information necessary for conducting risk modeling,
including annual HAP emissions estimates from individual emission
points at facilities and the related emissions release parameters. For
each emission record that was needed for the model input file for the
risk assessment (hereafter referred to as the ``RTR emissions
dataset'') that was not available from the 2011 ICR responses, the EPA
used available data in the 2011 NEI as the first alternative. The NEI
emission records used included annual HAP emissions estimates for
boilers, engines, chemical manufacturing processes, secondary metal
production processes, heaters, soil remediation, transportation
equipment, waste disposal, welding and other miscellaneous
manufacturing processes that were not included in the 2011 ICR.
Individual chromium emissions estimates were excluded from the modeling
file if they were found to overlap with a regulated process.
The 2005 NATA also provided supplemental data for the RTR emissions
dataset for this RTR. The 2005 NATA includes annual HAP emissions
estimates for three Aerospace Manufacturing and Rework Facilities that
are not in the 2011 NEI. These data were incorporated into the RTR
emissions dataset, and include emission data for space heaters, boilers
and underground fuel tanks at the facilities. Although the 2005 NATA
data is outdated, we thought it important to ensure we had accounted
for all the major sources in the source category and given that we did
not have data on three of the facilities, EPA augmented our RTR
emissions dataset with this data for three of the 144 facilities. We
expect to have updated NATA soon and will consider the impact on the
three sources, as appropriate. NATA is the EPA's ongoing evaluation of
air toxics in the United States. The EPA developed NATA as a screening
tool for state/local/tribal agencies to prioritize pollutants, emission
sources and locations of interest for further study in order to gain a
better understanding of population risks. NATA assessments do not
incorporate refined information about emission sources, but rather use
general information about sources to develop estimates of risks which
are more likely to overestimate impacts than underestimate them. NATA
provides estimates of the risk of cancer and other serious health
effects from breathing (inhaling) air toxics in order to inform both
national and more localized efforts to identify and prioritize air
toxics, emission source types and locations which are of greatest
potential concern in terms of contributing to population risk.
E. What litigation is related to this proposed action?
In 2007, the United States Court of Appeals for the District of
Columbia Circuit found that the EPA had erred in establishing emissions
standards for sources of HAP in the NESHAP for Brick and Structural
Clay Products Manufacturing and Clay Ceramics Manufacturing, 67 FR
26690 (May 16, 2003), and consequently vacated the rules.\3\ Among
other things, the court found EPA erred by failing to regulate
processes that emitted HAP, in some instances by establishing a MACT
floor of ``no control.'' In this action we are proposing to correct the
same error in the Aerospace NESHAP by proposing to remove the exemption
for specialty coatings found at 40 CFR 63.741(f) and instead add limits
for specialty coatings (including adhesives, adhesive bonding primers
and sealants).
---------------------------------------------------------------------------
\3\ Sierra Club v. EPA, 479 F. 3d 875 (D.C. Cir. March 13,
2007).
---------------------------------------------------------------------------
In a separate case, the court vacated portions of two provisions in
the EPA's CAA section 112 regulations that govern emissions of HAP
during periods of SSM.\4\ Specifically, the court vacated the SSM
exemption contained in 40 CFR 63.6(f)(1) and 40 CFR 63.6(h)(1), holding
that under section 302(k) of the CAA, emissions standards or
limitations must be continuous in nature and that the SSM exemption
violates the CAA's requirement that some section 112 standards apply
continuously. In this action, we are also proposing to revise these
provisions for Aerospace Manufacturing and Rework Facilities
operations, as discussed in section IV.E.2 of this preamble.
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\4\ Sierra Club v. EPA, 551 F. 3d 1019 (D.C. Cir. 2008), cert.
denied, 130 S. Ct 1735 (2010).
---------------------------------------------------------------------------
III. Analytical Procedures
In this section, we describe the analyses performed to support the
proposed decisions for the RTR and other issues addressed in this
proposal.
A. How did we estimate post-MACT risks posed by the source category?
The EPA conducted a risk assessment that provides estimates of the
MIR posed by the HAP emissions from each source in the source category,
the hazard index (HI) for chronic exposures to HAP with the potential
to cause non-cancer health effects and the hazard quotient (HQ) for
acute exposures to HAP with the potential to cause non-cancer health
effects. The assessment also provides estimates of the distribution of
cancer risks within the exposed populations, cancer incidence and an
evaluation of the potential for adverse environmental effects. The
seven sections that follow this paragraph describe how we estimated
emissions and conducted the risk assessment. The docket for this
rulemaking contains the following document that provides more
information on the risk assessment inputs and models: Residual Risk
Assessment for the Aerospace Manufacturing and Rework Facilities Source
Category in Support of the January, 2015 Risk and Technology Review
Proposal, January 2015. The methods used to assess risks (as described
in the primary steps below) are consistent with those peer-reviewed by
a panel of the EPA's Science Advisory Board (SAB) in 2009 and described
in their peer review report issued in 2010;\5\ they are also consistent
with the key recommendations contained in that report.
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\5\ U.S. EPA SAB. Risk and Technology Review (RTR) Risk
Assessment Methodologies: For Review by the EPA's Science Advisory
Board with Case Studies--MACT I Petroleum Refining Sources and
Portland Cement Manufacturing, May 2010.
---------------------------------------------------------------------------
1. How did we estimate actual emissions and identify the emissions
release characteristics?
Data for 144 Aerospace Manufacturing and Rework Facilities were
used to create the RTR emissions dataset, as described in section II.C
of this preamble. The emissions sources included in the RTR emissions
dataset includes the following types of sources currently regulated by
the Aerospace NESHAP: Primer/topcoat application operations, waste
handling operations, chemical milling maskant application
[[Page 8400]]
operations, cleaning operations and chemical and blast depainting
operations. The RTR emissions dataset also includes the following types
of sources not currently regulated by the Aerospace NESHAP: Specialty
coatings, composite processing, chemical milling and metal finishing,
wastewater, storage tanks, boilers, engines, chemical manufacturing
processes, secondary metal production processes, heaters, soil
remediation, transportation equipment, waste disposal, welding and
other miscellaneous manufacturing processes. These emission sources
include both fugitive emissions and stack emissions. This RTR emissions
dataset is based primarily on data gathered through the CAA section 114
questionnaire, as described in section II.C of this preamble. This
dataset was supplemented with data received from the 2012 ICR for stack
testing data and the 2013 request for information on coatings analyses
(as described in section II.C of this preamble), the 2011 NEI (as
described in section II.D of this preamble) and the 2005 NATA (as
described in section II.D of this preamble). The sources noted above
provided all of the emissions data in the RTR emissions dataset and
nearly all of the facility specific data needed to conduct the risk
modeling analysis. However, there were limited instances where default
values were used to fill gaps in the facility-specific data used in the
risk modeling analysis. Examples of default values used to fill these
data gaps were default values used for stack height and other release
point parameters, and percentages used to segregate mercury and
chromium compounds into separate species. Use of defaults is discussed
in detail in the memorandum, Aerospace Manufacturing and Rework
Facilities RTR Modeling File Preparation, December 2014, available in
the docket for this action (Modeling File Preparation Memo).
The RTR emissions dataset was refined following an extensive
quality assurance check of source locations, emission release
characteristics and annual emission estimates. We checked the
coordinates of each emission source in the dataset using ArcGIS to
ensure the emission point locations were correct. Also, as discussed in
section II.C of this preamble, in May 2014, the EPA solicited industry
review of the dataset and made corrections, as needed. For further
information on the EPA's quality assurance review, see the Modeling
File Preparation Memo available in the docket for this action.
A list of the 144 facilities and additional information used to
develop the RTR emissions dataset is available in the Aerospace RTR
database, and documentation on the development of this database is
provided in the Modeling File Preparation Memo, both of which are
available in the docket for this action.
2. How did we estimate MACT-allowable emissions?
The available emissions data in the RTR emissions dataset include
estimates of the actual mass of HAP emitted during the specified annual
time period. In some cases, these ``actual'' emission levels are lower
than the emission levels required to comply with the MACT standards.
The emissions level allowed to be emitted by the MACT standards is
referred to as the ``MACT-allowable'' emissions level. We discussed the
use of both MACT-allowable and actual emissions in the final Coke Oven
Batteries residual risk rule (70 FR 19998-19999, April 15, 2005) and in
the proposed and final Hazardous Organic NESHAP residual risk rules (71
FR 34428, June 14, 2006 and 71 FR 76609, December 21, 2006,
respectively). In those previous actions, we noted that assessing the
risks at the MACT-allowable level is inherently reasonable since these
risks reflect the maximum level facilities could emit and still comply
with national emission standards. We also explained that it is
reasonable to consider actual emissions, where such data are available,
in both steps of the risk analysis, in accordance with the Benzene
NESHAP approach. (54 FR 38044, September 14, 1989.)
We used the RTR emissions dataset discussed in section III.A.1 of
this preamble to estimate MACT-allowable emissions levels. Facilities
were asked to provide a multiplier in the 2011 ICR survey to scale up
average hourly emissions to maximum hourly emissions for air dispersion
modeling, given that each facility typically has a large number of
emission points and it would be difficult to determine the maximum
hourly emissions from each emission point. Many of the facilities
reported multipliers that were based on, for example, scaling
production from 2,000 hours to 8,760 hours per year or from one shift
per day to three shifts. However, using these values would have led to
unrealistically high ``allowable'' emission values because of
limitations in the market for new aerospace vehicles and for rework
services, and because many facilities have permit restrictions on their
total annual emissions. Therefore, the EPA did not use maximum hourly
emissions and instead chose to use a multiplier based on current and
historical industry capacity utilization factors. The EPA chose to use
a single multiplier of 1.02 to scale average annual emissions to
allowable annual emissions. The allowable emissions multiplier is based
on the difference between 2008 production utilization rate of 83.1
percent and the 20-year historical maximum production utilization rate
from 1990 of 85.0 percent (85 / 83.1 = 1.02). The docket for this
rulemaking contains information on the development of estimated MACT-
allowable emissions in the Modeling File Preparation Memo.
3. How did we conduct dispersion modeling, determine inhalation
exposures and estimate individual and population inhalation risks?
Both long-term and short-term inhalation exposure concentrations
and health risks from the source category addressed in this proposal
were estimated using the Human Exposure Model (Community and Sector
HEM-3 version 1.1.0). The HEM-3 performs three primary risk assessment
activities: (1) Conducting dispersion modeling to estimate the
concentrations of HAP in ambient air, (2) estimating long-term and
short-term inhalation exposures to individuals residing within 50
kilometers (km) of the modeled sources \6\ and (3) estimating
individual and population-level inhalation risks using the exposure
estimates and quantitative dose-response information.
---------------------------------------------------------------------------
\6\ This metric comes from the Benzene NESHAP. See 54 FR 38046.
---------------------------------------------------------------------------
The air dispersion model used in the analysis, the AERMOD model, is
one of the EPA's preferred models for assessing pollutant
concentrations from industrial facilities.\7\ To perform the dispersion
modeling and to develop the preliminary risk estimates, HEM-3 draws on
three data libraries. The first is a library of meteorological data,
which is used for dispersion calculations. This library includes 1 year
(2011) of hourly surface and upper air observations for more than 800
meteorological stations, selected to provide coverage of the United
States and Puerto Rico. A second library of United States Census Bureau
census block \8\ internal point locations and populations provides the
basis of human exposure calculations (U.S. Census, 2010). In addition,
for each census block, the census library
[[Page 8401]]
includes the elevation and controlling hill height, which are also used
in dispersion calculations. A third library of pollutant unit risk
factors and other health benchmarks is used to estimate health risks.
These risk factors and health benchmarks are the latest values
recommended by the EPA for HAP and other toxic air pollutants. These
values are available at: https://www.epa.gov/ttn/atw/toxsource/summary.html and are discussed in more detail later in this section.
---------------------------------------------------------------------------
\7\ U.S. EPA. Revision to the Guideline on Air Quality Models:
Adoption of a Preferred General Purpose (Flat and Complex Terrain)
Dispersion Model and Other Revisions (70 FR 68218, November 9,
2005).
\8\ A census block is the smallest geographic area for which
census statistics are tabulated.
---------------------------------------------------------------------------
In developing the risk assessment for chronic exposures, we used
the estimated annual average ambient air concentrations of each HAP
emitted by each source for which we have emissions data in the source
category. The air concentrations at each nearby census block centroid
were used as a surrogate for the chronic inhalation exposure
concentration for all the people who reside in that census block. We
calculated the MIR for each facility as the cancer risk associated with
a continuous lifetime (24 hours per day, 7 days per week and 52 weeks
per year for a 70-year period) exposure to the maximum concentration at
the centroid of inhabited census blocks. Individual cancer risks were
calculated by multiplying the estimated lifetime exposure to the
ambient concentration of each of the HAP (in micrograms per cubic meter
([mu]g/m\3\)) by its unit risk estimate (URE). The URE is an upper
bound estimate of an individual's probability of contracting cancer
over a lifetime of exposure to a concentration of 1 microgram of the
pollutant per cubic meter of air. For residual risk assessments, we
generally use URE values from the EPA's Integrated Risk Information
System (IRIS). For carcinogenic pollutants without IRIS values, we look
to other reputable sources of cancer dose-response values, often using
California EPA (CalEPA) URE values, where available. In cases where
new, scientifically credible dose response values have been developed
in a manner consistent with the EPA guidelines and have undergone a
peer review process similar to that used by the EPA, we may use such
dose-response values in place of, or in addition to, other values, if
appropriate.
The EPA estimated incremental individual lifetime cancer risks
associated with emissions from the facilities in the source category as
the sum of the risks for each of the carcinogenic HAP (including those
classified as carcinogenic to humans, likely to be carcinogenic to
humans and suggestive evidence of carcinogenic potential \9\) emitted
by the modeled sources. Cancer incidence and the distribution of
individual cancer risks for the population within 50 km of the sources
were also estimated for the source category as part of this assessment
by summing individual risks. A distance of 50 km is consistent with
both the analysis supporting the 1989 Benzene NESHAP (54 FR 38044,
September 14, 1989) and the limitations of Gaussian dispersion models,
including AERMOD.
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\9\ These classifications also coincide with the terms ``known
carcinogen, probable carcinogen, and possible carcinogen,''
respectively, which are the terms advocated in the EPA's previous
Guidelines for Carcinogen Risk Assessment, published in 1986 (51 FR
33992, September 24, 1986). Summing the risks of these individual
compounds to obtain the cumulative cancer risks is an approach that
was recommended by the EPA's SAB in their 2002 peer review of EPA's
NATA entitled, NATA--Evaluating the National-scale Air Toxics
Assessment 1996 Data--an SAB Advisory, available at: https://
yosemite.epa.gov/sab/sabproduct.nsf/
214C6E915BB04E14852570CA007A682C/$File/ecadv02001.pdf.
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To assess the risk of non-cancer health effects from chronic
exposures, we summed the HQ for each of the HAP that affects a common
target organ system to obtain the HI for that target organ system (or
target organ-specific HI, TOSHI). The HQ is the estimated exposure
divided by the chronic reference value, which is a value selected from
one of several sources. First, the chronic reference level can be the
EPA reference concentration (RfC) (https://www.epa.gov/riskassessment/glossary.htm), defined as ``an estimate (with uncertainty spanning
perhaps an order of magnitude) of a continuous inhalation exposure to
the human population (including sensitive subgroups) that is likely to
be without an appreciable risk of deleterious effects during a
lifetime.'' Alternatively, in cases where an RfC from the EPA's IRIS
database is not available or where the EPA determines that using a
value other than the RfC is appropriate, the chronic reference level
can be a value from the following prioritized sources: (1) The Agency
for Toxic Substances and Disease Registry (ATSDR) Minimum Risk Level
(https://www.atsdr.cdc.gov/mrls/index.asp), which is defined as ``an
estimate of daily human exposure to a hazardous substance that is
likely to be without an appreciable risk of adverse non-cancer health
effects (other than cancer) over a specified duration of exposure'';
(2) the CalEPA Chronic Reference Exposure Level (REL) (https://www.oehha.ca.gov/air/hot_spots/pdf/HRAguidefinal.pdf), which is defined
as ``the concentration level (that is expressed in units of micrograms
per cubic meter ([mu]g/m\3\) for inhalation exposure and in a dose
expressed in units of milligram per kilogram-day for oral exposures),
at or below which no adverse health effects are anticipated for a
specified exposure duration''; or (3), as noted above, a scientifically
credible dose-response value that has been developed in a manner
consistent with the EPA guidelines and has undergone a peer review
process similar to that used by the EPA, in place of or in concert with
other values.
As mentioned above, in order to characterize non-cancer chronic
effects, and in response to key recommendations from the SAB, the EPA
selects dose-response values that reflect the best available science
for all HAP included in RTR risk assessments.\10\ More specifically,
for a given HAP, the EPA examines the availability of inhalation
reference values from the sources included in our tiered approach
(e.g., IRIS first, ATSDR second, CalEPA third) and determines which
inhalation reference value represents the best available science. Thus,
as new inhalation reference values become available, the EPA will
typically evaluate them and determine whether they should be given
preference over those currently being used in RTR risk assessments.
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\10\ The SAB peer review of RTR Risk Assessment Methodologies is
available at: https://yosemite.epa.gov/sab/sabproduct.nsf/
4AB3966E263D943A8525771F00668381/$File/EPA-SAB-10-007-unsigned.pdf.
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The EPA also evaluated screening estimates of acute exposures and
risks for each of the HAP at the point of highest potential off-site
exposure for each facility. To do this, the EPA estimated the risks
when both the peak hourly emissions rate and worst-case dispersion
conditions occur. We also assume that a person is located at the point
of highest impact during that same time. In accordance with our mandate
in section 112 of the CAA, we use the point of highest off-site
exposure to assess the potential risk to the maximally exposed
individual. The acute HQ is the estimated acute exposure divided by the
acute dose-response value. In each case, the EPA calculated acute HQ
values using best available, short-term dose-response values. These
acute dose-response values, which are described below, include the
acute REL, acute exposure guideline levels (AEGL) and emergency
response planning guidelines (ERPG) for 1-hour exposure durations. As
discussed below, we used conservative assumptions for emissions rates,
meteorology and exposure location for our acute analysis.
[[Page 8402]]
As described in the CalEPA's Air Toxics Hot Spots Program Risk
Assessment Guidelines, Part I, The Determination of Acute Reference
Exposure Levels for Airborne Toxicants, an acute REL value (https://www.oehha.ca.gov/air/pdf/acuterel.pdf) is defined as ``the
concentration level at or below which no adverse health effects are
anticipated for a specified exposure duration.'' Id. at page 2. Acute
REL values are based on the most sensitive, relevant, adverse health
effect reported in the peer-reviewed medical and toxicological
literature. Acute REL values are designed to protect the most sensitive
individuals in the population through the inclusion of margins of
safety. Because margins of safety are incorporated to address data gaps
and uncertainties, exceeding the REL does not automatically indicate an
adverse health impact.
AEGL values were derived in response to recommendations from the
National Research Council (NRC). As described in Standing Operating
Procedures (SOP) of the National Advisory Committee on Acute Exposure
Guideline Levels for Hazardous Substances (https://www.epa.gov/oppt/aegl/pubs/sop.pdf),\11\ ``the NRC's previous name for acute exposure
levels--community emergency exposure levels--was replaced by the term
AEGL to reflect the broad application of these values to planning,
response and prevention in the community, the workplace,
transportation, the military and the remediation of Superfund sites.''
Id. at 2. This document also states that AEGL values ``represent
threshold exposure limits for the general public and are applicable to
emergency exposures ranging from 10 minutes to eight hours.'' Id. at 2.
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\11\ National Academy of Sciences (NAS), 2001. Standing
Operating Procedures for Developing Acute Exposure Levels for
Hazardous Chemicals, page 2.
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The document lays out the purpose and objectives of AEGL by stating
that ``the primary purpose of the AEGL program and the National
Advisory Committee for Acute Exposure Guideline Levels for Hazardous
Substances is to develop guideline levels for once-in-a-lifetime,
short-term exposures to airborne concentrations of acutely toxic, high-
priority chemicals.'' Id. at 21. In detailing the intended application
of AEGL values, the document states that ``[i]t is anticipated that the
AEGL values will be used for regulatory and nonregulatory purposes by
U.S. federal and state agencies and possibly the international
community in conjunction with chemical emergency response, planning and
prevention programs. More specifically, the AEGL values will be used
for conducting various risk assessments to aid in the development of
emergency preparedness and prevention plans, as well as real-time
emergency response actions, for accidental chemical releases at fixed
facilities and from transport carriers.'' Id. at 31.
The AEGL-1 value is then specifically defined as ``the airborne
concentration (expressed as ppm (parts per million) or mg/m\3\
(milligrams per cubic meter)) of a substance above which it is
predicted that the general population, including susceptible
individuals, could experience notable discomfort, irritation, or
certain asymptomatic nonsensory effects. However, the effects are not
disabling and are transient and reversible upon cessation of
exposure.'' Id. at 3. The document also notes that, ``Airborne
concentrations below AEGL-1 represent exposure levels that can produce
mild and progressively increasing but transient and nondisabling odor,
taste, and sensory irritation or certain asymptomatic, nonsensory
effects.'' Id. Similarly, the document defines AEGL-2 values as ``the
airborne concentration (expressed as parts per million or milligrams
per cubic meter) of a substance above which it is predicted that the
general population, including susceptible individuals, could experience
irreversible or other serious, long-lasting adverse health effects or
an impaired ability to escape.'' Id.
ERPG values are derived for use in emergency response, as described
in the American Industrial Hygiene Association's Emergency Response
Planning Committee document titled, ERPGS Procedures and
Responsibilities (https://sp4m.aiha.org/insideaiha/GuidelineDevelopment/ERPG/Documents/ERP-SOPs2006.pdf), which states that, ``Emergency
Response Planning Guidelines were developed for emergency planning and
are intended as health based guideline concentrations for single
exposures to chemicals.'' \12\ Id. at 1. The ERPG-1 value is defined as
``the maximum airborne concentration below which it is believed that
nearly all individuals could be exposed for up to 1 hour without
experiencing other than mild transient adverse health effects or
without perceiving a clearly defined, objectionable odor.'' Id. at 2.
Similarly, the ERPG-2 value is defined as ``the maximum airborne
concentration below which it is believed that nearly all individuals
could be exposed for up to one hour without experiencing or developing
irreversible or other serious health effects or symptoms which could
impair an individual's ability to take protective action.'' Id. at 1.
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\12\ ERP Committee Procedures and Responsibilities. November 1,
2006. American Industrial Hygiene Association.
---------------------------------------------------------------------------
As can be seen from the definitions above, the AEGL and ERPG values
include the similarly defined severity levels 1 and 2. For many
chemicals, a severity level 1 value AEGL or ERPG has not been developed
because the types of effects for these chemicals are not consistent
with the AEGL-1/ERPG-1 definitions; in these instances, we compare
higher severity level AEGL-2 or ERPG-2 values to our modeled exposure
levels to screen for potential acute concerns. When AEGL-1/ERPG-1
values are available, they are used in our acute risk assessments.
Acute REL values for 1-hour exposure durations are typically lower
than their corresponding AEGL-1 and ERPG-1 values. Even though their
definitions are slightly different, AEGL-1 values are often the same as
the corresponding ERPG-1 values, and AEGL-2 values are often equal to
ERPG-2 values. Maximum HQ values from our acute screening risk
assessments typically result when basing them on the acute REL value
for a particular pollutant. In cases where our maximum acute HQ value
exceeds 1, we also report the HQ value based on the next highest acute
dose-response value (usually the AEGL-1 and/or the ERPG-1 value).
To develop screening estimates of acute exposures in the absence of
hourly emissions data, generally we first develop estimates of maximum
hourly emissions rates by multiplying the average actual annual hourly
emissions rates by a default factor to cover routinely variable
emissions. We choose the factor to use partially based on process
knowledge and engineering judgment. The factor chosen also reflects a
Texas study of short-term emissions variability, which showed that most
peak emission events in a heavily-industrialized four-county area
(Harris, Galveston, Chambers and Brazoria Counties, Texas) were less
than twice the annual average hourly emissions rate. The highest peak
emissions event was 74 times the annual average hourly emissions rate,
and the 99th percentile ratio of peak hourly emissions rate to the
annual average hourly emissions rate was 9.\13\ Considering this
analysis, to account for more than 99 percent of the peak hourly
[[Page 8403]]
emissions, we apply a conservative screening multiplication factor of
10 to the average annual hourly emissions rate in our acute exposure
screening assessments as our default approach. However, we use a factor
other than 10 if we have information that indicates that a different
factor is appropriate for a particular source category.
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\13\ See https://www.tceq.state.tx.us/compliance/field_ops/eer/ or the docket to access the source of these data.
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For this source category, the default value was not utilized. A
peak 1-hour emission multiplier of 1.2 times the annual emissions was
utilized for the entire source category. This value was developed from
current and historical industry capacity utilization factors. The
emissions from this category are generally dependent on the amount of
HAP in the coatings and the amount of coating applied, and would only
vary in a significant manner if production increased. Therefore, the
EPA based the acute emissions multiplier on potential changes in
production. The acute emissions multiplier is based on the difference
between 2008 production utilization rate of 83.1 percent and the
maximum production utilization rate of 100 percent, which has not been
realized in 20 years of historical data (100 / 83.1 = 1.2). The docket
for this rulemaking contains information on the development of
estimated MACT-acute emissions in the Modeling File Preparation Memo. A
further discussion of why this factor was chosen can be found in
Appendix 1 of the Modeling File Preparation Memo, available in the
docket for this rulemaking.
As part of our acute risk assessment process, for cases where acute
HQ values from the screening step were less than or equal to 1 (even
under the conservative assumptions of the screening analysis), acute
impacts were deemed negligible and no further analysis was performed.
In cases where an acute HQ from the screening step was greater than 1,
additional site-specific data were considered to develop a more refined
estimate of the potential for acute impacts of concern. For this source
category, the data refinements employed consisted of evaluating the
off-site extent of any exceedances of the acute health benchmarks.
These refinements are discussed more fully in the Modeling File
Preparation Memo, which is available in the docket for this source
category. Ideally, we would prefer to have continuous measurements over
time to see how the emissions vary by each hour over an entire year.
Having a frequency distribution of hourly emissions rates over a year
would allow us to perform a probabilistic analysis to estimate
potential threshold exceedances and their frequency of occurrence. Such
an evaluation could include a more complete statistical treatment of
the key parameters and elements adopted in this screening analysis.
Recognizing that this level of data is rarely available, we instead
rely on the multiplier approach.
To better characterize the potential health risks associated with
estimated acute exposures to HAP, and in response to a key
recommendation from the SAB's peer review of the EPA's RTR risk
assessment methodologies,\14\ we generally examine a wider range of
available acute health metrics (e.g., RELs, AEGLs) than we do for our
chronic risk assessments. This is in response to the SAB's
acknowledgement that there are generally more data gaps and
inconsistencies in acute reference values than there are in chronic
reference values. In some cases, when Reference Value Arrays \15\ for
HAP have been developed, we consider additional acute values (i.e.,
occupational and international values) to provide a more complete risk
characterization.
---------------------------------------------------------------------------
\14\ The SAB peer review of RTR Risk Assessment Methodologies is
available at: https://yosemite.epa.gov/sab/sabproduct.nsf/
4AB3966E263D943A8525771F00668381/$File/EPA-SAB-10-007-unsigned.pdf.
\15\ U.S. EPA. (2009) Chapter 2.9, Chemical Specific Reference
Values for Formaldehyde, in Graphical Arrays of Chemical-Specific
Health Effect Reference Values for Inhalation Exposures (Final
Report). U.S. Environmental Protection Agency, Washington, DC, EPA/
600/R-09/061, and available online at https://cfpub.epa.gov/ncea/cfm/recordisplay.cfm?deid=211003.
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4. How did we conduct the multipathway exposure and risk screening?
The EPA conducted a screening analysis examining the potential for
significant human health risks due to exposures via routes other than
inhalation (i.e., ingestion). We first determined whether any sources
in the Aerospace Manufacturing and Rework Facilities source category
emitted any HAP known to be persistent and bioaccumulative in the
environment (PB-HAP). The PB-HAP compounds or compound classes are
identified for the screening from the EPA's Air Toxics Risk Assessment
Library (available at https://www2.epa.gov/fera/risk-assessment-and-modeling-air-toxics-risk-assessment-reference-library).
For the Aerospace Manufacturing and Rework Facilities source
category, we identified emissions of cadmium, dioxins/furans, POM,
mercury (both inorganic mercury and methyl mercury) and lead compounds.
Because one or more of these PB-HAP are emitted by at least one
facility in the Aerospace Manufacturing and Rework Facilities source
category, we proceeded to the next step of the evaluation. In this
step, we determined whether the facility-specific emissions rates of
the emitted PB-HAP were large enough to create the potential for
significant non-inhalation human health risks under reasonable worst-
case conditions. To facilitate this step, we developed emissions rate
screening levels for several PB-HAP using a hypothetical upper-end
screening exposure scenario developed for use in conjunction with the
EPA's Total Risk Integrated Methodology.Fate, Transport, and Ecological
Exposure (TRIM.FaTE) model. The PB-HAP with emissions rate screening
levels are: Lead, cadmium, chlorinated dibenzodioxins and furans,
mercury compounds and POM. We conducted a sensitivity analysis on the
screening scenario to ensure that its key design parameters would
represent the upper end of the range of possible values, such that it
would represent a conservative, but not impossible scenario. The
facility-specific emissions rates of these PB-HAP were compared to the
emission rate screening levels for these PB-HAP to assess the potential
for significant human health risks via non-inhalation pathways. We call
this application of the TRIM.FaTE model the Tier 1 TRIM-screen or Tier
1 screen.
For the purpose of developing emissions rates for our Tier 1 TRIM-
screen, we derived emission levels for these PB-HAP (other than lead
compounds) at which the maximum excess lifetime cancer risk would be 1-
in-1 million (i.e., for polychlorinated dibenzodioxins and furans and
POM) or, for HAP that cause non-cancer health effects (i.e., cadmium
compounds and mercury compounds), the maximum HQ would be 1. If the
emissions rate of any PB-HAP included in the Tier 1 screen exceeds the
Tier 1 screening emissions rate for any facility, we conduct a second
screen, which we call the Tier 2 TRIM-screen or Tier 2 screen.
In the Tier 2 screen, the location of each facility that exceeded
the Tier 1 emission rate is used to refine the assumptions associated
with the environmental scenario while maintaining the exposure scenario
assumptions. A key assumption that is part of the Tier 1 screen is that
a lake is located near the facility; we confirm the existence of lakes
near the facility as part of the Tier 2 screen. We then adjust the
risk-based Tier 1 screening level for each PB-HAP for each facility
based on an understanding of how exposure concentrations estimated for
the screening scenario change with meteorology and environmental
assumptions. PB-HAP emissions that do
[[Page 8404]]
not exceed these new Tier 2 screening levels are considered to pose no
unacceptable risks. If the PB-HAP emissions for a facility exceed the
Tier 2 screening emissions rate and data are available, we may decide
to conduct a more refined Tier 3 multipathway assessment. There are
several analyses that can be included in a Tier 3 screen depending upon
the extent of refinement warranted, including validating that the lake
is fishable and considering plume-rise to estimate emissions lost above
the mixing layer. If the Tier 3 screen is exceeded, the EPA may further
refine the assessment.
In evaluating the potential multipathway risk from emissions of
lead compounds, rather than developing a screening emissions rate for
them, we compared maximum estimated chronic inhalation exposures with
the level of the current National Ambient Air Quality Standard (NAAQS)
for lead.\16\ Values below the level of the primary (health-based) lead
NAAQS were considered to have a low potential for multipathway risk.
---------------------------------------------------------------------------
\16\ In doing so, EPA notes that the legal standard for a
primary NAAQS--that a standard is requisite to protect public health
and provide an adequate margin of safety (CAA section 109(b))--
differs from the CAA section 112(f) standard (requiring among other
things that the standard provide an ``ample margin of safety'').
However, the lead NAAQS is a reasonable measure of determining risk
acceptability (i.e., the first step of the Benzene NESHAP analysis)
since it is designed to protect the most susceptible group in the
human population--children, including children living near major
lead emitting sources (73 FR 67002/3; 73 FR 67000/3; 73 FR 67005/1).
In addition, applying the level of the primary lead NAAQS at the
risk acceptability step is conservative, since that primary lead
NAAQS reflects an adequate margin of safety.
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For further information on the multipathway analysis approach, see
the Residual Risk Assessment for the Aerospace Manufacturing and Rework
Facilities Source Category in Support of the January, 2015 Risk and
Technology Review Proposal, January 2015, which is available in the
docket for this action.
5. How did we conduct the environmental risk screening assessment?
a. Adverse Environmental Effect
The EPA conducts a screening assessment to examine the potential
for adverse environmental effects as required under section
112(f)(2)(A) of the CAA. Section 112(a)(7) of the CAA defines ``adverse
environmental effect'' as ``any significant and widespread adverse
effect, which may reasonably be anticipated, to wildlife, aquatic life
or other natural resources, including adverse impacts on populations of
endangered or threatened species or significant degradation of
environmental quality over broad areas.''
b. Environmental HAP
The EPA focuses on seven HAP, which we refer to as ``environmental
HAP,'' in its screening analysis: Five PB-HAP and two acid gases. The
five PB-HAP are cadmium, dioxins/furans, POM, mercury (both inorganic
mercury and methyl mercury) and lead compounds. The two acid gases are
hydrogen chloride (HCl) and hydrogen fluoride (HF). The rationale for
including these seven HAP in the environmental risk screening analysis
is presented below.
HAP that persist and bioaccumulate are of particular environmental
concern because they accumulate in the soil, sediment and water. The
PB-HAP are taken up, through sediment, soil, water and/or ingestion of
other organisms, by plants or animals (e.g., small fish) at the bottom
of the food chain. As larger and larger predators consume these
organisms, concentrations of the PB-HAP in the animal tissues increases
as does the potential for adverse effects. The five PB-HAP we evaluate
as part of our screening analysis account for 99.8 percent of all PB-
HAP emissions nationally from stationary sources (on a mass basis from
the 2005 NEI).
In addition to accounting for almost all of the mass of PB-HAP
emitted, we note that the TRIM.FaTE model that we use to evaluate
multipathway risk allows us to estimate concentrations of cadmium
compounds, dioxins/furans, POM and mercury in soil, sediment and water.
For lead compounds, we currently do not have the ability to calculate
these concentrations using the TRIM.FaTE model. Therefore, to evaluate
the potential for adverse environmental effects from lead compounds, we
compare the estimated HEM-modeled exposures from the source category
emissions of lead with the level of the secondary NAAQS for lead.\17\
We consider values below the level of the secondary NAAQS for lead to
be unlikely to cause adverse environmental effects.
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\17\ The secondary NAAQS for lead is a reasonable measure of
determining whether there is an adverse environmental effect since
it was established considering ``effects on soils, water, crops,
vegetation, man-made materials, animals, wildlife, weather,
visibility and climate, damage to and deterioration of property, and
hazards to transportation, as well as effects on economic values and
on personal comfort and well-being.''
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Due to their well-documented potential to cause direct damage to
terrestrial plants, we include two acid gases, HCl and HF, in the
environmental screening analysis. According to the 2005 NEI, HCl and HF
account for about 99 percent (on a mass basis) of the total acid gas
HAP emitted by stationary sources in the U.S. In addition to the
potential to cause direct damage to plants, high concentrations of HF
in the air have been linked to fluorosis in livestock. Air
concentrations of these HAP are already calculated as part of the human
multipathway exposure and risk screening analysis using the HEM3-AERMOD
air dispersion model, and we are able to use the air dispersion
modeling results to estimate the potential for an adverse environmental
effect.
The EPA acknowledges that other HAP beyond the seven HAP discussed
above may have the potential to cause adverse environmental effects.
Therefore, the EPA may include other relevant HAP in its environmental
risk screening in the future, as modeling science and resources allow.
The EPA invites comment on the extent to which other HAP emitted by the
source category may cause adverse environmental effects. Such
information should include references to peer-reviewed ecological
effects benchmarks that are of sufficient quality for making regulatory
decisions, as well as information on the presence of organisms located
near facilities within the source category that such benchmarks
indicate could be adversely affected.
c. Ecological Assessment Endpoints and Benchmarks for PB-HAP
An important consideration in the development of the EPA's
screening methodology is the selection of ecological assessment
endpoints and benchmarks. Ecological assessment endpoints are defined
by the ecological entity (e.g., aquatic communities including fish and
plankton) and its attributes (e.g., frequency of mortality). Ecological
assessment endpoints can be established for organisms, populations,
communities or assemblages and ecosystems.
For PB-HAP (other than lead compounds), we evaluated the following
community-level ecological assessment endpoints to screen for organisms
directly exposed to HAP in soils, sediment and water:
Local terrestrial communities (i.e., soil invertebrates,
plants) and populations of small birds and mammals that consume soil
invertebrates exposed to PB-HAP in the surface soil.
Local benthic (i.e., bottom sediment dwelling insects,
amphipods, isopods and crayfish) communities exposed to
[[Page 8405]]
PB-HAP in sediment in nearby water bodies.
Local aquatic (water-column) communities (including fish
and plankton) exposed to PB-HAP in nearby surface waters.
For PB-HAP (other than lead compounds), we also evaluated the
population-level ecological assessment endpoint to screen for indirect
HAP exposures of top consumers via the bioaccumulation of HAP in food
chains. The endpoint evaluated was piscivorous (i.e., fish-eating)
wildlife consuming PB-HAP-contaminated fish from nearby water bodies.
For cadmium compounds, dioxins/furans, POM and mercury, we
identified the available ecological benchmarks for each assessment
endpoint. An ecological benchmark represents a concentration of HAP
(e.g., 0.77 [micro]g of HAP per liter of water) that has been linked to
a particular environmental effect level (e.g., a no-observed-adverse-
effect level (NOAEL)) through scientific study. For PB-HAP, we
identified, where possible, ecological benchmarks at the following
effect levels:
Probable effect levels (PEL): Level above which adverse
effects are expected to occur frequently.
Lowest-observed-adverse-effect level (LOAEL): The lowest
exposure level tested at which there are biologically significant
increases in frequency or severity of adverse effects.
No-observed-adverse-effect levels (NOAEL): The highest
exposure level tested at which there are no biologically significant
increases in the frequency or severity of adverse effect.
We established a hierarchy of preferred benchmark sources to allow
selection of benchmarks for each environmental HAP at each ecological
assessment endpoint. In general, the EPA sources that are used at a
programmatic level (e.g., Office of Water, Superfund Program) were
used, if available. If not, the EPA benchmarks used in regional
programs (e.g., Superfund) were used. If benchmarks were not available
at a programmatic or regional level, we used benchmarks developed by
other federal agencies (e.g., National Oceanic and Atmospheric
Administration (NOAA)) or state agencies.
Benchmarks for all effect levels are not available for all PB-HAP
and assessment endpoints. In cases where multiple effect levels were
available for a particular PB-HAP and assessment endpoint, we use all
of the available effect levels to help us to determine whether
ecological risks exist and, if so, whether the risks could be
considered significant and widespread.
d. Ecological Assessment Endpoints and Benchmarks for Acid Gases
The environmental screening analysis also evaluated potential
damage and reduced productivity of plants due to direct exposure to
acid gases in the air. For acid gases, we evaluated the ecological
assessment endpoint of local terrestrial plant communities with foliage
exposed to acidic gaseous HAP in the air.
The selection of ecological benchmarks for the effects of acid
gases on plants followed the same approach as for PB-HAP (i.e., we
examine all of the available chronic benchmarks). For HCl, the EPA
identified chronic benchmark concentrations. We note that the benchmark
for chronic HCl exposure to plants is greater than the reference
concentration for chronic inhalation exposure for human health. This
means that where the EPA includes regulatory requirements to prevent an
exceedance of the reference concentration for human health, additional
analyses for adverse environmental effects of HCl would not be
necessary.
For HF, the EPA identified chronic benchmark concentrations for
plants and evaluated chronic exposures to plants in the screening
analysis. High concentrations of HF in the air have also been linked to
fluorosis in livestock. However, the HF concentrations at which
fluorosis in livestock occur are higher than those at which plant
damage begins. Therefore, the benchmarks for plants are protective of
both plants and livestock.
e. Screening Methodology
For the environmental risk screening analysis, the EPA first
determined whether any facilities in the Aerospace Manufacturing and
Rework Facilities source category emitted any of the seven
environmental HAP. For the Aerospace Manufacturing and Rework
Facilities source category, we identified emissions of five PB-HAP and
two acid gases as the environmental HAP. The five PB-HAP are cadmium,
dioxins/furans, POM, mercury (both inorganic mercury and methyl
mercury) and lead compounds. The two acid gases are HCl and HF.
Because one or more of the seven environmental HAP evaluated are
emitted by at least one facility in the source category, we proceeded
to the second step of the evaluation.
f. PB-HAP Methodology
For cadmium, mercury, POM and dioxins/furans, the environmental
screening analysis consists of two tiers, while lead compounds are
analyzed differently as discussed earlier. In the first tier, we
determined whether the maximum facility-specific emission rates of each
of the emitted environmental HAP were large enough to create the
potential for adverse environmental effects under reasonable worst-case
environmental conditions. These are the same environmental conditions
used in the human multipathway exposure and risk screening analysis.
To facilitate this step, TRIM.FaTE was run for each PB-HAP under
hypothetical environmental conditions designed to provide
conservatively high HAP concentrations. The model was set to maximize
runoff from terrestrial parcels into the modeled lake, which in turn,
maximized the chemical concentrations in the water, the sediments and
the fish. The resulting media concentrations were then used to back-
calculate a screening level emission rate that corresponded to the
relevant exposure benchmark concentration value for each assessment
endpoint. To assess emissions from a facility, the reported emission
rate for each PB-HAP was compared to the screening level emission rate
for that PB-HAP for each assessment endpoint. If emissions from a
facility do not exceed the Tier 1 screening level, the facility
``passes'' the screen, and, therefore, is not evaluated further under
the screening approach. If emissions from a facility exceed the Tier 1
screening level, we evaluate the facility further in Tier 2.
In Tier 2 of the environmental screening analysis, the emission
rate screening levels are adjusted to account for local meteorology and
the actual location of lakes in the vicinity of facilities that did not
pass the Tier 1 screen. The modeling domain for each facility in the
Tier 2 analysis consists of eight octants. Each octant contains five
modeled soil concentrations at various distances from the facility (5
soil concentrations x 8 octants = total of 40 soil concentrations per
facility) and one lake with modeled concentrations for water, sediment
and fish tissue. In the Tier 2 environmental risk screening analysis,
the 40 soil concentration points are averaged to obtain an average soil
concentration for each facility for each PB-HAP. For the water,
sediment and fish tissue concentrations, the highest value for each
facility for each pollutant is used. If emission concentrations from a
facility do not exceed the Tier 2 screening level, the facility passes
the screen, and typically is not evaluated further. If emissions from a
facility exceed the Tier 2 screening level, the facility does not
[[Page 8406]]
pass the screen and, therefore, may have the potential to cause adverse
environmental effects. Such facilities are evaluated further to
investigate factors such as the magnitude and characteristics of the
area of exceedance.
g. Acid Gas Methodology
The environmental screening analysis evaluates the potential
phytotoxicity and reduced productivity of plants due to chronic
exposure to acid gases. The environmental risk screening methodology
for acid gases is a single-tier screen that compares the average off-
site ambient air concentration over the modeling domain to ecological
benchmarks for each of the acid gases. Because air concentrations are
compared directly to the ecological benchmarks, emission-based
screening levels are not calculated for acid gases as they are in the
ecological risk screening methodology for PB-HAP.
For purposes of ecological risk screening, the EPA identifies a
potential for adverse environmental effects to plant communities from
exposure to acid gases when the average concentration of the HAP around
a facility exceeds the LOAEL ecological benchmark. In such cases, we
further investigate factors such as the magnitude and characteristics
of the area of exceedance (e.g., land use of exceedance area, size of
exceedance area) to determine if there is an adverse environmental
effect.
For further information on the environmental screening analysis
approach, see the Residual Risk Assessment for the Aerospace
Manufacturing and Rework Facilities Source Category in Support of the
January, 2015 Risk and Technology Review Proposal, January 2015, which
is available in the docket for this action.
6. How did we conduct facility-wide assessments?
To put the source category risks in context, we typically examine
the risks from the entire ``facility,'' where the facility includes all
HAP-emitting operations within a contiguous area and under common
control. In other words, we examine the HAP emissions not only from the
source category emission points of interest, but also emissions of HAP
from all other emission sources at the facility for which we have data.
The emissions inventories developed from the 2011 and 2012 ICRs,
2011 NEI and 2005 NATA include emissions information for all emissions
sources at the facilities that are part of the Aerospace Manufacturing
and Rework Facilities source category. These include sources currently
regulated by the Aerospace NESHAP: Primer/topcoat application
operations, waste handling operations, chemical milling maskant
application operations, cleaning operations and chemical and blast
depainting operations. These also include emission sources not
currently regulated by the Aerospace NESHAP: Specialty coatings,
composite processing, chemical milling and metal finishing, wastewater,
storage tanks, boilers, engines, chemical manufacturing processes,
secondary metal production processes, heaters, soil remediation,
transportation equipment, waste disposal, welding and other
miscellaneous manufacturing processes.
We analyzed risks due to the inhalation of HAP that are emitted
``facility-wide'' for the populations residing within 50 km of each
facility, consistent with the methods used for the source category
analysis described above. For these facility-wide risk analyses, the
modeled source category risks were compared to the facility-wide risks
to determine the portion of facility-wide risks that could be
attributed to the source category addressed in this proposal. We
specifically examined the facility that was associated with the highest
estimate of risk and determined the percentage of that risk
attributable to the source category of interest. The Residual Risk
Assessment for the Aerospace Manufacturing and Rework Facilities Source
Category in Support of the January, 2015 Risk and Technology Review
Proposal, January 2015, available through the docket for this action,
provides the methodology and results of the facility-wide analyses,
including all facility-wide risks and the percentage of source category
contribution to facility-wide risks.
7. How did we consider uncertainties in risk assessment?
In the Benzene NESHAP, we concluded that risk estimation
uncertainty should be considered in our decision-making under the ample
margin of safety framework. Uncertainty and the potential for bias are
inherent in all risk assessments, including those performed for this
proposal. Although uncertainty exists, we believe that our approach,
which used conservative tools and assumptions, ensures that our
decisions are health protective and environmentally protective. A brief
discussion of the uncertainties in the RTR emissions dataset,
dispersion modeling, inhalation exposure estimates and dose-response
relationships follows below. A more thorough discussion of these
uncertainties is included in the Residual Risk Assessment for the
Aerospace Manufacturing and Rework Facilities Source Category in
Support of the January, 2015 Risk and Technology Review Proposal,
January 2015, which is available in the docket for this action.
a. Uncertainties in the RTR Emissions Dataset
Although the development of the RTR emissions dataset involved
quality assurance/quality control processes, the accuracy of emissions
values will vary depending on the source of the data, the degree to
which data are incomplete or missing, the degree to which assumptions
made to complete the datasets are accurate, and errors in emission
estimates and other factors. The emission estimates considered in this
analysis are annual totals for certain years, and they do not reflect
short-term fluctuations during the course of a year or variations from
year to year. The estimates of peak hourly emission rates for the acute
effects screening assessment were based on an emission adjustment
factor applied to the average annual hourly emission rates, which are
intended to account for emission fluctuations due to normal facility
operations.
b. Uncertainties in Dispersion Modeling
We recognize there is uncertainty in ambient concentration
estimates associated with any model, including the EPA's recommended
regulatory dispersion model, AERMOD. In using a model to estimate
ambient pollutant concentrations, the user chooses certain options to
apply. For RTR assessments, we select some model options that have the
potential to overestimate ambient air concentrations (e.g., not
including plume depletion or pollutant transformation). We select other
model options that have the potential to underestimate ambient impacts
(e.g., not including building downwash). Other options that we select
have the potential to either under- or overestimate ambient levels
(e.g., meteorology and receptor locations). On balance, considering the
directional nature of the uncertainties commonly present in ambient
concentrations estimated by dispersion models, the approach we apply in
the RTR assessments should yield unbiased estimates of ambient HAP
concentrations.
c. Uncertainties in Inhalation Exposure
The EPA did not include the effects of human mobility on exposures
in the assessment. Specifically, short-term mobility and long-term
mobility between census blocks in the modeling
[[Page 8407]]
domain were not considered.\18\ The approach of not considering short
or long-term population mobility does not bias the estimate of the
theoretical MIR (by definition), nor does it affect the estimate of
cancer incidence because the total population number remains the same.
It does, however, affect the shape of the distribution of individual
risks across the affected population, shifting it toward higher
estimated individual risks at the upper end and reducing the number of
people estimated to be at lower risks, thereby increasing the estimated
number of people at specific high risk levels (e.g., 1-in-10 thousand
or 1-in-1 million).
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\18\ Short-term mobility is movement from one micro-environment
to another over the course of hours or days. Long-term mobility is
movement from one residence to another over the course of a
lifetime.
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In addition, the assessment predicted the chronic exposures at the
centroid of each populated census block as surrogates for the exposure
concentrations for all people living in that block. Using the census
block centroid to predict chronic exposures tends to over-predict
exposures for people in the census block who live farther from the
facility and under-predict exposures for people in the census block who
live closer to the facility. Thus, using the census block centroid to
predict chronic exposures may lead to a potential understatement or
overstatement of the true maximum impact, but is an unbiased estimate
of average risk and incidence. We reduce this uncertainty by analyzing
large census blocks near facilities using aerial imagery and adjusting
the location of the block centroid to better represent the population
in the block, as well as adding additional receptor locations where the
block population is not well represented by a single location.
The assessment evaluates the cancer inhalation risks associated
with pollutant exposures over a 70-year period, which is the assumed
lifetime of an individual. In reality, both the length of time that
modeled emission sources at facilities actually operate (i.e., more or
less than 70 years) and the domestic growth or decline of the modeled
industry (i.e., the increase or decrease in the number or size of
domestic facilities) will influence the future risks posed by a given
source or source category. Depending on the characteristics of the
industry, these factors will, in most cases, result in an overestimate
both in individual risk levels and in the total estimated number of
cancer cases. However, in the unlikely scenario where a facility
maintains, or even increases, its emissions levels over a period of
more than 70 years, residents live beyond 70 years at the same
location, and the residents spend most of their days at that location,
then the cancer inhalation risks could potentially be underestimated.
However, annual cancer incidence estimates from exposures to emissions
from these sources would not be affected by the length of time an
emissions source operates.
The exposure estimates used in these analyses assume chronic
exposures to ambient (outdoor) levels of pollutants. Because most
people spend the majority of their time indoors, actual exposures may
not be as high, depending on the characteristics of the pollutants
modeled. For many of the HAP, indoor levels are roughly equivalent to
ambient levels, but for very reactive pollutants or larger particles,
indoor levels are typically lower. This factor has the potential to
result in an overestimate of 25 to 30 percent of exposures.\19\
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\19\ U.S. EPA. National-Scale Air Toxics Assessment for 1996.
EPA 453/R-01-003; January 2001; page 85.
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In addition to the uncertainties highlighted above, there are
several factors specific to the acute exposure assessment that the EPA
conducts as part of the risk review under section 112 of the CAA that
should be highlighted. The accuracy of an acute inhalation exposure
assessment depends on the simultaneous occurrence of independent
factors that may vary greatly, such as hourly emissions rates,
meteorology and the presence of humans at the location of the maximum
concentration. In the acute screening assessment that we conduct under
the RTR program, we assume that peak emissions from the source category
and worst-case meteorological conditions co-occur, thus, resulting in
maximum ambient concentrations. These two events are unlikely to occur
at the same time, making these assumptions conservative. We then
include the additional assumption that a person is located at this
point during this same time period. For this source category, these
assumptions would tend to be worst-case actual exposures as it is
unlikely that a person would be located at the point of maximum
exposure during the time when peak emissions and worst-case
meteorological conditions occur simultaneously.
d. Uncertainties in Dose-Response Relationships
There are uncertainties inherent in the development of the dose-
response values used in our risk assessments for cancer effects from
chronic exposures and non-cancer effects from both chronic and acute
exposures. Some uncertainties may be considered quantitatively, and
others generally are expressed in qualitative terms. We note as a
preface to this discussion a point on dose-response uncertainty that is
brought out in the EPA's 2005 Cancer Guidelines; namely, that ``the
primary goal of EPA actions is protection of human health; accordingly,
as an Agency policy, risk assessment procedures, including default
options that are used in the absence of scientific data to the
contrary, should be health protective'' (EPA 2005 Cancer Guidelines,
pages 1-7). This is the approach followed here as summarized in the
next several paragraphs. A complete detailed discussion of
uncertainties and variability in dose-response relationships is given
in the Residual Risk Assessment for the Aerospace Manufacturing and
Rework Facilities Source Category in Support of the January, 2015 Risk
and Technology Review Proposal, January 2015, which is available in the
docket for this action.
Cancer URE values used in our risk assessments are those that have
been developed to generally provide an upper bound estimate of risk.
That is, they represent a ``plausible upper limit to the true value of
a quantity'' (although this is usually not a true statistical
confidence limit).\20\ In some circumstances, the true risk could be as
low as zero; however, in other circumstances the risk could be
greater.\21\ When developing an upper bound estimate of risk and to
provide risk values that do not underestimate risk, health-protective
default approaches are generally used. To err on the side of ensuring
adequate health protection, the EPA typically uses the upper bound
estimates rather than lower bound or central tendency estimates in our
risk assessments, an approach that may have limitations for other uses
(e.g., priority-setting or expected benefits analysis).
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\20\ IRIS glossary (https://www.epa.gov/NCEA/iris/help_gloss.htm).
\21\ An exception to this is the URE for benzene, which is
considered to cover a range of values, each end of which is
considered to be equally plausible, and which is based on maximum
likelihood estimates.
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Chronic non-cancer RfC and reference dose (RfD) values represent
chronic exposure levels that are intended to be health-protective
levels. Specifically, these values provide an estimate (with
uncertainty spanning perhaps an order of magnitude) of a continuous
inhalation exposure (RfC) or a daily oral exposure (RfD) to the human
population
[[Page 8408]]
(including sensitive subgroups) that is likely to be without an
appreciable risk of deleterious effects during a lifetime. To derive
values that are intended to be ``without appreciable risk,'' the
methodology relies upon an uncertainty factor (UF) approach (U.S. EPA,
1993, 1994) 22 23 which considers uncertainty, variability
and gaps in the available data. The UF are applied to derive reference
values that are intended to protect against appreciable risk of
deleterious effects. The UF are commonly default values \24\ (e.g.,
factors of 10 or 3) used in the absence of compound-specific data;
where data are available, UF may also be developed using compound-
specific information. When data are limited, more assumptions are
needed and more UF are used. Thus, there may be a greater tendency to
overestimate risk in the sense that further study might support
development of reference values that are higher (i.e., less potent)
because fewer default assumptions are needed. However, for some
pollutants, it is possible that risks may be underestimated.
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\22\ U.S. EPA. Reference Dose (RfD): Description and Use in
Health Risk Assessments. Dated March 1993.
\23\ U.S. EPA. Methods for Derivation of Inhalation Reference
Concentrations and Application of Inhalation Dosimetry. EPA/600/8-
90/066F. Dated October 1994.
\24\ According to the NRC report, Science and Judgment in Risk
Assessment (NRC, 1994) ``[Default] options are generic approaches,
based on general scientific knowledge and policy judgment, that are
applied to various elements of the risk assessment process when the
correct scientific model is unknown or uncertain.'' The 1983 NRC
report, Risk Assessment in the Federal Government: Managing the
Process, defined default option as ``the option chosen on the basis
of risk assessment policy that appears to be the best choice in the
absence of data to the contrary'' (NRC, 1983a, p. 63). Therefore,
default options are not rules that bind the agency; rather, the
agency may depart from them in evaluating the risks posed by a
specific substance when it believes this to be appropriate. In
keeping with EPA's goal of protecting public health and the
environment, default assumptions are used to ensure that risk to
chemicals is not underestimated (although defaults are not intended
to overtly overestimate risk). See EPA, 2004, An Examination of EPA
Risk Assessment Principles and Practices, EPA/100/B-04/001 available
at: https://www.epa.gov/osa/pdfs/ratf-final.pdf.
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While collectively termed ``UF,'' these factors account for a
number of different quantitative considerations when using observed
animal (usually rodent) or human toxicity data in the development of
the RfC. The UF are intended to account for: (1) Variation in
susceptibility among the members of the human population (i.e., inter-
individual variability); (2) uncertainty in extrapolating from
experimental animal data to humans (i.e., interspecies differences);
(3) uncertainty in extrapolating from data obtained in a study with
less-than-lifetime exposure (i.e., extrapolating from sub-chronic to
chronic exposure); (4) uncertainty in extrapolating the observed data
to obtain an estimate of the exposure associated with no adverse
effects; and (5) uncertainty when the database is incomplete or there
are problems with the applicability of available studies.
Many of the UF used to account for variability and uncertainty in
the development of acute reference values are quite similar to those
developed for chronic durations, but they more often use individual UF
values that may be less than 10. The UF are applied based on chemical-
specific or health effect-specific information (e.g., simple irritation
effects do not vary appreciably between human individuals, hence a
value of 3 is typically used), or based on the purpose for the
reference value (see the following paragraph). The UF applied in acute
reference value derivation include: (1) Heterogeneity among humans; (2)
uncertainty in extrapolating from animals to humans; (3) uncertainty in
lowest observed adverse effect (exposure) level to no observed adverse
effect (exposure) level adjustments; and (4) uncertainty in accounting
for an incomplete database on toxic effects of potential concern.
Additional adjustments are often applied to account for uncertainty in
extrapolation from observations at one exposure duration (e.g., 4
hours) to derive an acute reference value at another exposure duration
(e.g., 1 hour).
Not all acute reference values are developed for the same purpose
and care must be taken when interpreting the results of an acute
assessment of human health effects relative to the reference value or
values being exceeded. Where relevant to the estimated exposures, the
lack of short-term dose-response values at different levels of severity
should be factored into the risk characterization as potential
uncertainties.
For a group of compounds that are unspeciated (e.g., glycol
ethers), we conservatively use the most protective reference value of
an individual compound in that group to estimate risk. Similarly, for
an individual compound in a group (e.g., ethylene glycol diethyl ether)
that does not have a specified reference value, we also apply the most
protective reference value from the other compounds in the group to
estimate risk.
e. Uncertainties in the Multipathway Assessment
For each source category, we generally rely on site-specific levels
of PB-HAP emissions to determine whether a refined assessment of the
impacts from multipathway exposures is necessary. This determination is
based on the results of a three-tiered screening analysis that relies
on the outputs from models that estimate environmental pollutant
concentrations and human exposures for four PB-HAP. Two important types
of uncertainty associated with the use of these models in RTR risk
assessments and inherent to any assessment that relies on environmental
modeling are model uncertainty and input uncertainty.\25\
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\25\ In the context of this discussion, the term ``uncertainty''
as it pertains to exposure and risk encompasses both variability in
the range of expected inputs and screening results due to existing
spatial, temporal and other factors, as well as uncertainty in being
able to accurately estimate the true result.
---------------------------------------------------------------------------
Model uncertainty concerns whether the selected models are
appropriate for the assessment being conducted and whether they
adequately represent the actual processes that might occur for that
situation. An example of model uncertainty is the question of whether
the model adequately describes the movement of a pollutant through the
soil. This type of uncertainty is difficult to quantify. However, based
on feedback received from previous EPA SAB reviews and other reviews,
we are confident that the models used in the screen are appropriate and
state-of-the-art for the multipathway risk assessments conducted in
support of RTR.
Input uncertainty is concerned with how accurately the models have
been configured and parameterized (i.e., represented in terms of
measurable or estimable variables) for the assessment at hand. For Tier
1 of the multipathway screen, we configured the models to avoid
underestimating exposure and risk. This was accomplished by selecting
upper-end values from nationally representative datasets for the more
influential parameters in the environmental model, including selection
and spatial configuration of the area of interest, lake location and
size, meteorology, surface water and soil characteristics and structure
of the aquatic food web. We also assume an ingestion exposure scenario
and values for human exposure factors that represent reasonable maximum
exposures.
In Tier 2 of the multipathway assessment, we refine the model
inputs to account for meteorological patterns in the vicinity of the
facility versus using upper-end national values and we identify the
actual location of lakes near the facility rather than the default lake
location that we apply in Tier 1. By
[[Page 8409]]
refining the screening approach in Tier 2 to account for local
geographical and meteorological data, we decrease the likelihood that
concentrations in environmental media are overestimated, thereby
increasing the usefulness of the screen. The assumptions and the
associated uncertainties regarding the selected ingestion exposure
scenario are the same for Tier 1 and Tier 2.
For both Tiers 1 and 2 of the multipathway assessment, our approach
to addressing model input uncertainty is generally cautious. We choose
model inputs from the upper end of the range of possible values for the
influential parameters used in the models, and we assume that the
exposed individual exhibits ingestion behavior that would lead to a
high total exposure. This approach reduces the likelihood of not
identifying high risks for adverse impacts.
Despite the uncertainties, when individual pollutants or facilities
do screen out, we are confident that the potential for adverse
multipathway impacts on human health is very low. On the other hand,
when individual pollutants or facilities do not screen out, it does not
mean that multipathway impacts are significant, only that we cannot
rule out that possibility and that a refined multipathway analysis for
the site might be necessary to obtain a more accurate risk
characterization for the source category.
For further information on uncertainties and the Tier 1 and 2
screening methods, refer to Appendix 4 of Modeling File Preparation
Memo.
f. Uncertainties in the Environmental Risk Screening Assessment
For each source category, we generally rely on site-specific levels
of environmental HAP emissions to perform an environmental screening
assessment. The environmental screening assessment is based on the
outputs from models that estimate environmental HAP concentrations. The
same models, specifically the TRIM.FaTE multipathway model and the
AERMOD air dispersion model, are used to estimate environmental HAP
concentrations for both the human multipathway screening analysis and
for the environmental screening analysis. Therefore, both screening
assessments have similar modeling uncertainties.
Two important types of uncertainty associated with the use of these
models in RTR environmental screening assessments--and inherent to any
assessment that relies on environmental modeling--are model uncertainty
and input uncertainty.\26\
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\26\ In the context of this discussion, the term
``uncertainty,'' as it pertains to exposure and risk assessment,
encompasses both variability in the range of expected inputs and
screening results due to existing spatial, temporal and other
factors, as well as uncertainty in being able to accurately estimate
the true result.
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Model uncertainty concerns whether the selected models are
appropriate for the assessment being conducted and whether they
adequately represent the movement and accumulation of environmental HAP
emissions in the environment. For example, does the model adequately
describe the movement of a pollutant through the soil? This type of
uncertainty is difficult to quantify. However, based on feedback
received from previous EPA SAB reviews and other reviews, we are
confident that the models used in the screen are appropriate and state-
of-the-art for the environmental risk assessments conducted in support
of our RTR analyses.
Input uncertainty is concerned with how accurately the models have
been configured and parameterized for the assessment at hand. For Tier
1 of the environmental screen for PB-HAP, we configured the models to
avoid underestimating exposure and risk to reduce the likelihood that
the results indicate the risks are lower than they actually are. This
was accomplished by selecting upper-end values from nationally-
representative datasets for the more influential parameters in the
environmental model, including selection and spatial configuration of
the area of interest, the location and size of any bodies of water,
meteorology, surface water and soil characteristics and structure of
the aquatic food web. In Tier 1, we used the maximum facility-specific
emissions for the PB-HAP (other than lead compounds, which were
evaluated by comparison to the secondary lead NAAQS) that were included
in the environmental screening assessment and each of the media when
comparing to ecological benchmarks. This is consistent with the
conservative design of Tier 1 of the screen. In Tier 2 of the
environmental screening analysis for PB-HAP, we refine the model inputs
to account for meteorological patterns in the vicinity of the facility
versus using upper-end national values, and we identify the locations
of water bodies near the facility location. By refining the screening
approach in Tier 2 to account for local geographical and meteorological
data, we decrease the likelihood that concentrations in environmental
media are overestimated, thereby increasing the usefulness of the
screen. To better represent widespread impacts, the modeled soil
concentrations are averaged in Tier 2 to obtain one average soil
concentration value for each facility and for each PB-HAP. For PB-HAP
concentrations in water, sediment and fish tissue, the highest value
for each facility for each pollutant is used.
For the environmental screening assessment for acid gases, we
employ a single-tiered approach. We use the modeled air concentrations
and compare those with ecological benchmarks.
For both Tiers 1 and 2 of the environmental screening assessment,
our approach to addressing model input uncertainty is generally
cautious. We choose model inputs from the upper end of the range of
possible values for the influential parameters used in the models, and
we assume that the exposed individual exhibits ingestion behavior that
would lead to a high total exposure. This approach reduces the
likelihood of not identifying potential risks for adverse environmental
impacts.
Uncertainty also exists in the ecological benchmarks for the
environmental risk screening analysis. We established a hierarchy of
preferred benchmark sources to allow selection of benchmarks for each
environmental HAP at each ecological assessment endpoint. In general,
EPA benchmarks for programmatic levels (e.g., Office of Water,
Superfund Program) were used if available. If not, we used EPA
benchmarks used in regional programs (e.g., Superfund Program). If
benchmarks were not available at a programmatic or regional level, we
used benchmarks developed by other agencies (e.g., NOAA) or by state
agencies.
In all cases (except for lead compounds, which were evaluated
through a comparison to the NAAQS), we searched for benchmarks at the
following three effect levels, as described in section III.A.5 of this
preamble:
1. A no-effect level (i.e., NOAEL).
2. Threshold-effect level (i.e., LOAEL).
3. Probable effect level (i.e., PEL).
For some ecological assessment endpoint/environmental HAP
combinations, we could identify benchmarks for all three effect levels,
but for most, we could not. In one case, where different agencies
derived significantly different numbers to represent a threshold for
effect, we included both. In several cases, only a single benchmark was
available. In cases where multiple effect levels were
[[Page 8410]]
available for a particular PB-HAP and assessment endpoint, we used all
of the available effect levels to help us to determine whether risk
exists and if the risks could be considered significant and widespread.
The EPA evaluates the following seven HAP in the environmental risk
screening assessment: Cadmium, dioxins/furans, POM, mercury (both
inorganic mercury and methyl mercury), lead compounds, HCl and HF,
where applicable. These seven HAP represent pollutants that can cause
adverse impacts for plants and animals either through direct exposure
to HAP in the air or through exposure to HAP that is deposited from the
air onto soils and surface waters. These seven HAP also represent those
HAP for which we can conduct a meaningful environmental risk screening
assessment. For other HAP not included in our screening assessment, the
model has not been parameterized such that it can be used for that
purpose. In some cases, depending on the HAP, we may not have
appropriate multipathway models that allow us to predict the
concentration of that pollutant. The EPA acknowledges that other HAP
beyond the seven HAP that we are evaluating may have the potential to
cause adverse environmental effects and, therefore, the EPA may
evaluate other relevant HAP in the future, as modeling science and
resources allow.
Further information on uncertainties and the Tier 1 and 2
environmental screening methods is provided in Appendix 5 of the
document, Technical Support Document for TRIM-Based Multipathway Tiered
Screening Methodology for RTR: Summary of Approach and Evaluation.
Also, see the Residual Risk Assessment for the Aerospace Manufacturing
and Rework Facilities Source Category in Support of the January, 2015
Risk and Technology Review Proposal, January 2015, available in the
docket for this action.
B. How did we consider the risk results in making decisions for this
proposal?
As discussed in section II.A of this preamble, in evaluating and
developing standards under CAA section 112(f)(2), we apply a two-step
process to address residual risk. In the first step, the EPA determines
whether risks are acceptable. This determination ``considers all health
information, including risk estimation uncertainty, and includes a
presumptive limit on maximum individual lifetime [cancer] risk (MIR)
\27\ of approximately [1-in-10 thousand] [i.e., 100-in-1 million].'' 54
FR 38045, September 14, 1989. If risks are unacceptable, the EPA must
determine the emissions standards necessary to bring risks to an
acceptable level without considering costs. In the second step of the
process, the EPA considers whether the emissions standards provide an
ample margin of safety ``in consideration of all health information,
including the number of persons at risk levels higher than
approximately 1-in-1 million, as well as other relevant factors,
including costs and economic impacts, technological feasibility, and
other factors relevant to each particular decision.'' Id. The EPA must
promulgate emission standards necessary to provide an ample margin of
safety.
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\27\ Although defined as ``maximum individual risk,'' MIR refers
only to cancer risk. MIR, one metric for assessing cancer risk, is
the estimated risk were an individual exposed to the maximum level
of a pollutant for a lifetime.
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In past residual risk actions, the EPA considered a number of human
health risk metrics associated with emissions from the categories under
review, including the MIR, the number of persons in various risk
ranges, cancer incidence, the maximum non-cancer HI and the maximum
acute non-cancer hazard. See, e.g., 72 FR 25138, May 3, 2007; 71 FR
42724, July 27, 2006. The EPA considered this health information for
both actual and allowable emissions. See, e.g., 75 FR 65068, October
21, 2010; 75 FR 80220, December 21, 2010; 76 FR 29032, May 19, 2011.
The EPA also discussed risk estimation uncertainties and considered the
uncertainties in the determination of acceptable risk and ample margin
of safety in these past actions. The EPA considered this same type of
information in support of this action.
The agency is considering these various measures of health
information to inform our determinations of risk acceptability and
ample margin of safety under CAA section 112(f). As explained in the
Benzene NESHAP, ``the first step judgment on acceptability cannot be
reduced to any single factor'' and, thus, ``[t]he Administrator
believes that the acceptability of risk under [previous] section 112 is
best judged on the basis of a broad set of health risk measures and
information.'' 54 FR 38046, September 14, 1989. Similarly, with regard
to the ample margin of safety determination, ``the Agency again
considers all of the health risk and other health information
considered in the first step. Beyond that information, additional
factors relating to the appropriate level of control will also be
considered, including cost and economic impacts of controls,
technological feasibility, uncertainties, and any other relevant
factors.'' Id.
The Benzene NESHAP approach provides flexibility regarding factors
the EPA may consider in making determinations and how the EPA may weigh
those factors for each source category. In responding to comment on our
policy under the Benzene NESHAP, the EPA explained that:
[t]he policy chosen by the Administrator permits consideration of
multiple measures of health risk. Not only can the MIR figure be
considered, but also incidence, the presence of non-cancer health
effects, and the uncertainties of the risk estimates. In this way,
the effect on the most exposed individuals can be reviewed as well
as the impact on the general public. These factors can then be
weighed in each individual case. This approach complies with the
Vinyl Chloride mandate that the Administrator ascertain an
acceptable level of risk to the public by employing [her] expertise
to assess available data. It also complies with the Congressional
intent behind the CAA, which did not exclude the use of any
particular measure of public health risk from the EPA's
consideration with respect to CAA section 112 regulations, and
thereby implicitly permits consideration of any and all measures of
health risk which the Administrator, in [her] judgment, believes are
appropriate to determining what will `protect the public health'.
See 54 FR at 38057, September 14, 1989. Thus, the level of the MIR is
only one factor to be weighed in determining acceptability of risks.
The Benzene NESHAP explained that ``an MIR of approximately 1-in-10
thousand should ordinarily be the upper end of the range of
acceptability. As risks increase above this benchmark, they become
presumptively less acceptable under CAA section 112, and would be
weighed with the other health risk measures and information in making
an overall judgment on acceptability. Or, the Agency may find, in a
particular case, that a risk that includes MIR less than the
presumptively acceptable level is unacceptable in the light of other
health risk factors.'' Id. at 38045. Similarly, with regard to the
ample margin of safety analysis, the EPA stated in the Benzene NESHAP
that: ``EPA believes the relative weight of the many factors that can
be considered in selecting an ample margin of safety can only be
determined for each specific source category. This occurs mainly
because technological and economic factors (along with the health-
related factors) vary from source category to source category.'' Id. at
38061. We also consider the uncertainties associated with the various
risk analyses, as discussed earlier in this preamble, in
[[Page 8411]]
our determinations of acceptability and ample margin of safety.
The EPA notes that it has not considered certain health information
to date in making residual risk determinations. At this time, we do not
attempt to quantify those HAP risks that may be associated with
emissions from other facilities that do not include the source
categories in question, mobile source emissions, natural source
emissions, persistent environmental pollution or atmospheric
transformation in the vicinity of the sources in these categories.
The agency understands the potential importance of considering an
individual's total exposure to HAP in addition to considering exposure
to HAP emissions from the source category and facility. We recognize
that such consideration may be particularly important when assessing
non-cancer risks, where pollutant-specific exposure health reference
levels (e.g., RfCs) are based on the assumption that thresholds exist
for adverse health effects. For example, the agency recognizes that,
although exposures attributable to emissions from a source category or
facility alone may not indicate the potential for increased risk of
adverse non-cancer health effects in a population, the exposures
resulting from emissions from the facility in combination with
emissions from all of the other sources (e.g., other facilities) to
which an individual is exposed may be sufficient to result in increased
risk of adverse non-cancer health effects. In May 2010, the SAB advised
the EPA ``that RTR assessments will be most useful to decision makers
and communities if results are presented in the broader context of
aggregate and cumulative risks, including background concentrations and
contributions from other sources in the area.'' \28\
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\28\ EPA's responses to this and all other key recommendations
of the SAB's advisory on RTR risk assessment methodologies (which is
available at: https://yosemite.epa.gov/sab/sabproduct.nsf/
4AB3966E263D943A8525771F00668381/$File/EPA-SAB-10-007-unsigned.pdf)
are outlined in a memo to this rulemaking docket from David Guinnup
entitled, EPA's Actions in Response to the Key Recommendations of
the SAB Review of RTR Risk Assessment Methodologies.
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In response to the SAB recommendations, the EPA is incorporating
cumulative risk analyses into its RTR risk assessments, including those
reflected in this proposal. The agency is: (1) Conducting facility-wide
assessments, which include source category emission points as well as
other emission points within the facilities; (2) considering sources in
the same category whose emissions result in exposures to the same
individuals; and (3) for some persistent and bioaccumulative
pollutants, analyzing the ingestion route of exposure. In addition, the
RTR risk assessments have always considered aggregate cancer risk from
all carcinogens and aggregate non-cancer hazard indices from all non-
carcinogens affecting the same target organ system.
Although we are interested in placing source category and facility-
wide HAP risks in the context of total HAP risks from all sources
combined in the vicinity of each source, we are concerned about the
uncertainties of doing so. Because of the contribution to total HAP
risk from emission sources other than those that we have studied in
depth during this RTR review, such estimates of total HAP risks would
have significantly greater associated uncertainties than the source
category or facility-wide estimates. Such aggregate or cumulative
assessments would compound those uncertainties, making the assessments
too unreliable.
C. How did we perform the technology review?
Our technology review focused on the identification and evaluation
of developments in practices, processes and control technologies that
have occurred since the MACT standards were promulgated. Where we
identified such developments, in order to inform our decision of
whether it is ``necessary'' to revise the emissions standards, we
analyzed the technical feasibility of applying these developments and
the estimated costs, energy implications, non-air environmental
impacts, as well as considering the emission reductions. We also
considered the appropriateness of applying controls to new sources
versus retrofitting existing sources.
Based on our analyses of the available data and information, we
identified potential developments in practices, processes and control
technologies. For this exercise, we considered any of the following to
be a ``development'':
Any add-on control technology or other equipment that was
not identified and considered during development of the original MACT
standards.
Any improvements in add-on control technology or other
equipment (that were identified and considered during development of
the original MACT standards) that could result in additional emissions
reduction.
Any work practice or operational procedure that was not
identified or considered during development of the original MACT
standards.
Any process change or pollution prevention alternative
that could be broadly applied to the industry and that was not
identified or considered during development of the original MACT
standards.
Any significant changes in the cost (including cost
effectiveness) of applying controls (including controls the EPA
considered during the development of the original MACT standards).
We reviewed a variety of data sources in our investigation of
potential practices, processes or controls to consider. Among the
sources we reviewed were the NESHAP for various industries that were
promulgated since the MACT standards being reviewed in this action. We
reviewed the regulatory requirements and/or technical analyses
associated with these regulatory actions to identify any practices,
processes and control technologies considered in these efforts that
could be applied to emission sources in the Aerospace Manufacturing and
Rework Facilities source category, as well as the costs, non-air
impacts and energy implications associated with the use of these
technologies. Additionally, we requested information from facilities
regarding developments in practices, processes or control technology.
Finally, we reviewed information from other sources, such as state and/
or local permitting agency databases and industry-supported databases.
IV. Analytical Results and Proposed Decisions
A. What actions are we taking pursuant to CAA sections 112(d)(2) and
112(d)(3)?
We are not proposing any new emissions limitations to the NESHAP
other than with respect to specialty coatings. In this action, we are
proposing the following revisions to the Aerospace NESHAP to ensure the
standards are consistent with the requirements of the CAA as
interpreted by the courts: adding standards to limit organic and
inorganic HAP emissions from specialty coating application operations
and updating the provisions regulating emissions during periods of SSM.
Additionally, we are adding an alternative compliance demonstration
provision for all types of coating application operations (primers,
topcoats, specialty coatings and chemical milling maskants) in certain
situations. The results and proposed decisions based on the analyses
performed pursuant to CAA section 112(d)(2) and (3) are presented
below.
We are proposing to establish MACT standards specific to specialty
coating application operations to ensure the standards are consistent
with the
[[Page 8412]]
requirements of the CAA as interpreted by the courts. Under CAA section
112(d)(3), the EPA is required to promulgate emissions limits for all
HAP emitted from major source categories.\29\ Specialty coatings are a
source of HAP emissions from the Aerospace Manufacturing and Rework
Facilities source category that is not currently regulated under the
Aerospace NESHAP. We are proposing organic HAP content limits to reduce
organic HAP emissions and equipment and work practice standards to
reduce inorganic HAP emissions associated with specialty coating
application. Refer to section IV.E.1 of this preamble for a description
of specialty coating application operations, associated emissions and
how this emissions source is addressed in the current Aerospace NESHAP,
and how the EPA established the MACT floor for specialty coating
application operations. Section IV.E.1 of this preamble also includes
the EPA's rationale for proposing this standard, as well as how the EPA
established the MACT floor for specialty coating application operations
and the estimated costs for complying with the proposed standard. The
EPA is proposing to add these standards for specialty coatings because
they are a source of HAP emissions from the Aerospace Manufacturing and
Rework Facilities source category and EPA had not previously
established MACT standards for these emissions points. These proposed
changes are necessary to ensure the emissions standards are consistent
with the requirements of the CAA as interpreted by the courts and are
unrelated to the risk findings.
---------------------------------------------------------------------------
\29\ For more details see the discussion of Sierra Club v. EPA,
479 F. 3d 875 (D.C. Cir. 2007) in section II.E of this preamble,
which found that the EPA may not set ``no emissions reductions''
MACT floors.
---------------------------------------------------------------------------
The EPA is also proposing to revise the provisions affecting
periods of SSM to clarify that the emission limitations in the
Aerospace NESHAP apply at all times, including during these SSM
periods. Refer to section IV.E.3 of this preamble for a description of
the EPA's proposed revisions to the SSM provisions for aerospace
manufacturing and rework operations. These proposed changes to the SSM
provisions are necessary to ensure the emissions standards are
consistent with the requirements of the CAA as interpreted by the
courts and are unrelated to the risk findings.
The EPA also collected emissions data and performed a risk analysis
for certain emissions points outside of the source category--chemical
milling and metal finishing operations, waste water operations, storage
tanks and composite operations that are related to aerospace
manufacturing and rework, but are not surface coating operations. The
data collected for these non-surface coating operations were used to
characterize the risk presented from these operations in order to
estimate the total risk from the entirety of each aerospace
manufacturing and rework facility. The EPA is not proposing to expand
the Aerospace Manufacturing and Rework Facilities source category to
include these operations, which are not surface coating operations and
were not part of the original source category and which, as explained
below, did not present unacceptable risks. The initial and subsequent
listings of source categories for regulation under section 112 of the
CAA included Aerospace Manufacturing and Rework Facilities only as a
surface coating source category.\30\ \31\
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\30\ Initial List of Categories of Sources Under Section
112(c)(1) of the Clean Air Act Amendments of 1990. 57 FR 31576, July
17, 1992.
\31\ National Emission Standards for Hazardous Air Pollutants;
Revision of Initial List of Categories of Sources and Schedule for
Standards Under Sections 112(c) and (e) of the Clean Air Act
Amendments of 1990. 61 FR 28197, June 4, 1996.
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B. What are the results of the risk assessment and analyses?
1. Inhalation Risk Assessment Results
Table 2 of this preamble provides an overall summary of the results
of the inhalation risk assessment.
Table 2--Aerospace Manufacturing and Rework Facilities Inhalation Risk Assessment Results
----------------------------------------------------------------------------------------------------------------
Estimated
Estimated population annual cancer Maximum
Maximum individual cancer at increased risk incidence chronic non- Maximum screening acute non-
risk (-in-1 million) \a\ levels of cancer (cases per cancer TOSHI cancer HQ \c\
year) \b\
----------------------------------------------------------------------------------------------------------------
Actual Emissions
----------------------------------------------------------------------------------------------------------------
10......................... >= 1-in-1 million: 0.02 0.5 HQREL = 2 (ethylene glycol
180,000. ethyl ether acetate).
>= 10-in-1 million:
1,500.
>= 100-in-1 million: 0
----------------------------------------------------------------------------------------------------------------
Allowable Emissions \d\
----------------------------------------------------------------------------------------------------------------
10......................... >= 1-in-1 million: 0.02 0.5 ...........................
180,000.
>= 10-in-1 million:
2,000.
>= 100-in-1 million: 0
----------------------------------------------------------------------------------------------------------------
\a\ Estimated maximum individual excess lifetime cancer risk due to HAP emissions from the source category.
\b\ Maximum TOSHI. The target organ with the highest TOSHI for the Aerospace Manufacturing and Rework Facilities
source category for both actual and allowable emissions is the kidney system.
\c\ See Section III.A.3 of this preamble for explanation of acute dose-response values. Acute assessments are
not performed on allowable emissions.
\d\ The development of allowable emission estimates can be found in the memorandum titled, Aerospace
Manufacturing and Rework Facilities RTR Modeling File Preparation, December 2014, which is available in the
docket.
The inhalation risk modeling performed to estimate risks based on
actual and allowable emissions relied primarily on emissions data from
the ICRs and calculations described in the memorandum titled, Aerospace
[[Page 8413]]
Manufacturing and Rework Facilities RTR Modeling File Preparation,
December 2014, which is available in the docket for this action. The
results of the chronic baseline inhalation cancer risk assessment
indicate that, based on estimates of current actual emissions, the MIR
posed by the Aerospace Manufacturing and Rework Facilities is 10-in-1
million, with emissions of strontium chromate, from coating operations
accounting for the majority of the risk. The total estimated cancer
incidence from Aerospace Manufacturing and Rework Facilities based on
actual emission levels is 0.02 excess cancer cases per year or one case
every 50 years, with emissions of strontium chromate and chromium
compounds contributing 66 percent and 15 percent, respectively, to the
cancer incidence. In addition, we note that approximately 1,500 people
are estimated to have cancer risks greater than or equal to 10-in-1
million, and approximately 180,000 people are estimated to have risks
greater than or equal to 1-in-1 million as a result of actual emissions
from this source category.
When considering MACT-allowable emissions, the MIR is estimated to
be up to 10-in-1 million, driven by emissions of strontium chromate
from coating operations. The estimated cancer incidence is estimated to
be 0.02 excess cancer cases per year, or one excess case in every 50
years. Approximately 2,000 people are estimated to have cancer risks
greater than or equal to 10-in-1 million and approximately 180,000
people are estimated to have cancer risks greater than or equal to 1-
in-1 million considering allowable emissions from Aerospace
Manufacturing and Rework Facilities.
The maximum modeled chronic non-cancer HI (TOSHI) value for the
source category based on actual emissions is estimated to be 0.5,
driven by cadmium compounds emissions from blast depainting. When
considering MACT-allowable emissions, the maximum chronic non-cancer
TOSHI value is estimated to be 0.5, also driven by cadmium compounds
emissions from blast depainting.
2. Acute Risk Results
Our screening analysis for worst-case acute impacts based on actual
emissions indicates the potential for one pollutant, ethylene glycol
ethyl ether acetate, from one facility, to have HQ values above 1,
based on its REL value. One hundred forty-three of the 144 Aerospace
Manufacturing and Rework Facilities had an estimated worst-case HQ less
than or equal to 1 for all HAP.
To better characterize the potential health risks associated with
estimated worst-case acute exposures to HAP from the source category at
issue and in response to a key recommendation from the SAB's peer
review of the EPA's CAA section 112(f) RTR risk assessment
methodologies, we examine a wider range of available acute health
metrics than we do for our chronic risk assessments. This is in
acknowledgement that there are generally more data gaps and
inconsistencies in acute reference values than there are in chronic
reference values.
By definition, the acute CalEPA REL represents a health-protective
level of exposure, with no risk anticipated below those levels, even
for repeated exposures; however, the health risk from higher-level
exposures is unknown. Therefore, when a CalEPA REL is exceeded and an
AEGL-1 or ERPG-1 level is available (i.e., levels at which mild effects
are anticipated in the general public for a single exposure), we have
used them as a second comparative measure. Historically, comparisons of
the estimated maximum off-site 1-hour exposure levels have not been
typically made to occupational levels for the purpose of characterizing
public health risks in RTR assessments. This is because occupational
ceiling values are not generally considered protective for the general
public since they are designed to protect the worker population
(presumed healthy adults) for short-duration (less than 15-minute)
increases in exposure. As a result, for most chemicals, the 15-minute
occupational ceiling values are set at levels higher than a 1-hour
AEGL-1, making comparisons to them irrelevant unless the AEGL-1 or
ERPG-1 levels are also exceeded.
The worst-case maximum estimated 1-hour exposure to ethylene glycol
ethyl ether acetate outside the facility fence line for the source
categories is 0.3 mg/m\3\. This estimated worst-case exposure exceeds
the 1-hour REL by a factor of 2 (HQREL = 2). All other HAP
in this analysis have worst-case acute HQ values of 1 or less (maximum
HQAEGL-1 = 0.02 for phenol, maximum HQERPG-1 =
0.03 for phenol) indicating that they carry no potential to pose acute
concerns.
In characterizing the potential for acute non-cancer impacts of
concern, it is important to remember the upward bias of these exposure
estimates (e.g., worst-case meteorology coinciding with a person
located at the point of maximum concentration during the hour) and to
consider the results along with the conservative estimates used to
develop peak hourly emissions as described in the Modeling File
Preparation Memo (which is available in the docket for this action) for
a detailed description of how the hourly emissions were developed for
this source category.
3. Multipathway Risk Screening Results
Results of the worst-case Tier I screening analysis indicate that
PB-HAP emissions of cadmium compounds or mercury compounds did not
exceed the screening emission rates. Neither dioxins nor polycyclic
aromatic hydrocarbons (PAH) are emitted by any source in the source
category.
4. Environmental Risk Screening Results
As described in section III.A of this preamble, we conducted a
screening-level evaluation of the potential adverse environmental risks
associated with emissions of the following environmental HAP from the
Aerospace Manufacturing and Rework Facilities source category: lead,
mercury, cadmium, HCl and HF.
In the Tier 1 screening analysis for PB-HAP (other than lead
compounds, which were evaluated differently), the individual modeled
Tier 1 concentrations for mercury and cadmium did not exceed any
ecological benchmark for any facility in the source category. For lead
compounds, we did not estimate any exceedances of the secondary lead
NAAQS.
For HF and HCl, the average modeled concentration around each
facility (i.e., the average concentration of all off-site data points
in the modeling domain) did not exceed the ecological benchmarks. In
addition, each individual modeled concentration of HCl and HF (i.e.,
each off-site data point in the modeling domain) was below the
ecological benchmarks for all facilities.
5. Facility-Wide Risk Results
The facility-wide chronic MIR and TOSHI were estimated based on
emissions from all sources at the identified facilities (both MACT and
non MACT sources). The results of the facility-wide assessment for
cancer risks indicate that 44 facilities with aerospace manufacturing
and rework processes have a facility-wide cancer MIR greater than or
equal to 1-in-1 million. The maximum facility-wide cancer MIR is 20-in-
1 million, primarily driven by arsenic and chromium (VI) compounds,
from internal combustion engines. The maximum facility-wide TOSHI for
the source category is estimated to be 0.5, primarily driven by
emissions of hexamethylene-1,6-diisocyanate from specialty coatings
operations.
[[Page 8414]]
6. What demographic groups might benefit from this regulation?
To examine the potential for any environmental justice (EJ) issues
that might be associated with the source category, we performed a
demographic analysis, which is an assessment of risks to individual
demographic groups, of the population close to the facilities. In this
analysis, we evaluated the distribution of HAP-related cancer risks and
non-cancer hazards from the Aerospace Manufacturing and Rework
Facilities across different social, demographic and economic groups
within the populations living near facilities identified as having the
highest risks. The methodology and the results of the demographic
analyses are included in a technical report, Risk and Technology
Review--Analysis of Socio-Economic Factors for Populations Living Near
Aerospace Facilities, available in the docket for this action.
The results of the demographic analysis are summarized in Table 3
of this preamble. These results, for various demographic groups, are
based on the estimated risks from actual aerospace manufacturing and
rework emissions levels for the population living within 50 km of the
facilities.
Table 3--Aerospace Manufacturing and Rework Facilities Demographic Risk Analysis Results
----------------------------------------------------------------------------------------------------------------
Population with Population
cancer risk at with chronic
or above 1-in-1 hazard index
Nationwide million due to above 1 due to
emissions from emissions from
aerospace aerospace
facilities facilities
----------------------------------------------------------------------------------------------------------------
Total Population............................................... 312,861,265 179,074 0
----------------------------------------------------------------------------------------------------------------
Race by Percent
----------------------------------------------------------------------------------------------------------------
White.......................................................... 72 64 NA
All Other Races................................................ 28 36 NA
----------------------------------------------------------------------------------------------------------------
Race by Percent
----------------------------------------------------------------------------------------------------------------
White.......................................................... 72 64 NA
African American............................................... 13 19 NA
Native American................................................ 1 1.5 NA
Other and Multiracial.......................................... 14 16 NA
----------------------------------------------------------------------------------------------------------------
Ethnicity by Percent
----------------------------------------------------------------------------------------------------------------
Hispanic....................................................... 17 16 NA
Non-Hispanic................................................... 83 84 NA
----------------------------------------------------------------------------------------------------------------
Income by Percent
----------------------------------------------------------------------------------------------------------------
Below Poverty Level............................................ 14 19 NA
Above Poverty Level............................................ 86 81 NA
----------------------------------------------------------------------------------------------------------------
Education by Percent
----------------------------------------------------------------------------------------------------------------
Over 25 and without High School Diploma........................ 15 17 NA
Over 25 and with a High School Diploma......................... 85 83 NA
----------------------------------------------------------------------------------------------------------------
The results of the Aerospace Manufacturing and Rework Facilities
baseline risk assessment indicate that emissions from the source
category expose approximately 180,000 people to a cancer risk at or
above 1-in-1 million and no one is predicted to have a chronic non-
cancer TOSHI greater than 1.
The analysis indicates that the percentages of the population
exposed to a cancer risk greater than or equal to 1-in-1 million and
living within 50 km of the 144 aerospace facilities is higher for
minority populations, 36-percent exposed versus the national minority
population average of 28 percent. The specific demographics of the
population within 50 km of the facilities indicate potential
disparities in certain demographic groups, including the ``African
American'' and ``Below the Poverty Level.''
C. What are our proposed decisions regarding risk acceptability, ample
margin of safety and adverse environmental effects?
1. Risk Acceptability
As noted in section II.A.1 of this preamble, the EPA sets standards
under CAA section 112(f)(2) using ``a two-step standard-setting
approach, with an analytical first step to determine an `acceptable
risk' that considers all health information, including risk estimation
uncertainty, and includes a presumptive limit on MIR of approximately 1
in 10 thousand.'' 54 FR 38045, September 14, 1989. For the Aerospace
Manufacturing and Rework Facilities source category, we estimate, based
on both actual and allowable emissions, an MIR of 10-in-1 million
driven by emissions of strontium chromate from coating operations. We
estimate that, based on actual emissions, about 1,500 people are
estimated to have cancer risks greater than or equal to 10-in-1 million
and, based on allowable emissions, about 2,000 people have cancer risks
greater than or equal to 10-in-1 million. We estimate that
approximately 180,000 people are estimated to have risks greater than
or equal to 1-in-1 million based on both actual and allowable emissions
from this source category. The total estimated incidence of cancer for
this source category due to inhalation exposures, based on both actual
and allowable emissions, is 0.02 excess cancer cases
[[Page 8415]]
per year, or 1 case in 50 years. The agency estimates that the maximum
chronic non-cancer TOSHI from inhalation exposure, based on both actual
and allowable emissions, from this source category, is 0.5, with
cadmium compounds emissions from blast depainting accounting for the
majority of the TOSHI.
The multipathway screening analysis, based upon actual emissions,
indicates that PB-HAP emissions of both cadmium compounds and mercury
compounds did not exceed the screening emission rates. Neither dioxins
nor PAH are emitted by any source in the source category. In evaluating
the potential for multipathway effects from emissions of lead, modeled
maximum annual lead concentrations were compared to the secondary NAAQS
for lead (0.15 [mu]g/m\3\). Results of this analysis estimate that the
NAAQS for lead would not be exceeded at any off-site locations.
The screening assessment of worst-case acute inhalation impacts
from baseline actual emissions indicates that the worst-case maximum
estimated 1-hour exposure to ethylene glycol ethyl ether acetate
outside the facility fence line exceeds the 1-hour REL by a factor of 2
(HQREL = 2). This exceedance was only predicted to occur in
a remote, non-inhabited area just adjacent to the facility fence line
for 2 hours a year. All other HAP in this analysis have worst-case
acute HQ values of 1 or less (maximum HQAEGL-1 = 0.02 for
phenol, maximum HQERPG-1 = 0.03 for phenol) indicating that
they carry no potential to pose acute concerns.
In determining whether risks are acceptable for this source
category, the EPA considered all available health information including
any uncertainty in risk estimates. Also, as noted above, the agency
estimated risk from both actual and allowable emissions. While there
are uncertainties associated with both the actual and allowable
emissions, we consider the allowable emissions to be an upper bound,
based on the conservative methods we used to calculate allowable
emissions.
The risk results indicate that both the actual and allowable
inhalation cancer risks to the individual most exposed are no greater
than approximately 10-in-1 million, which is considerably less than the
presumptive limit of acceptability (i.e., 100-in-1 million). The
maximum chronic non-cancer hazard indices for both the actual and
allowable inhalation non-cancer risks to the individual most exposed of
0.5 is less than 1.
The maximum acute non-cancer HQ for all pollutants was 2 based on
the REL for ethylene glycol ethyl ether acetate. This value was only
predicted to occur during 2 hours per year in a remote location
adjacent to a single facility's fenceline. All other acute risks are
estimated to be below a noncancer HI threshold of 1.
The multipathway screening analysis indicates that PB-HAP emissions
did not exceed the screening emission rates for any compound evaluated.
Considering all of the health risk information and factors
discussed above, including the uncertainties discussed in section
III.A.8 of this preamble, the EPA proposes that the risks at baseline
are acceptable since the cancer risks are well below the presumptive
limit of acceptability and the non-cancer results indicate there is
minimal likelihood of adverse non-cancer health effects due to HAP
emissions from this source category.
2. Ample Margin of Safety Analysis and Proposed Controls
Under the ample margin of safety analysis, we evaluate the cost and
feasibility of available control technologies and other measures
(including the controls, measures and costs evaluated under the
technology review) that could be applied in this source category to
further reduce the risks due to emissions of HAP identified in our risk
assessment, as well as the health impacts of such potential additional
measures. As noted in our discussion of the technology review in
section III.C of this preamble, no measures (beyond those already in
place or that we are proposing today under CAA sections 112 (d)(2) and
(d)(3)) were identified for reducing HAP emissions from the Aerospace
Manufacturing and Rework Facilities source category. Therefore, we
propose that the current standards provide an ample margin of safety to
protect public health.
Although the current standards were found to provide an ample
margin of safety to protect public health, we are proposing additional
standards under CAA sections 112(d)(2) and (3) that address previously
unregulated emissions of HAP from specialty coating application
operations. The additional standards are being proposed to address a
deficiency in the Aerospace NESHAP as discussed previously in section
II.E. of this preamble. We are proposing organic HAP and volatile
organic compound (VOC) content limits for specialty coatings that are
equal to the VOC content limits specified in the Aerospace CTG for
specialty coatings. Facilities that do not use specialty coatings and
those in nonattainment areas that are currently complying with the
Aerospace CTG limits for their specialty coating operations will not
have to do anything new to meet these requirements. The 74 facilities
located in attainment areas that reported using specialty coatings in
the 2011 ICR may not be using compliant coatings and may need to use
alternative coatings, direct the emissions stream to an add-on control
device or use the averaging option to demonstrate compliance with
implement the standards. We are also proposing that specialty coating
application operations be subject to the same equipment standards
(i.e., use high-efficiency application equipment) currently required
for primer and topcoat application operations. Further, we are
proposing to require that specialty coating application operations meet
current work practice standards for primer and topcoat application
operations for inorganic HAP emissions. The estimated emission
reductions resulting from these proposed HAP content limits, equipment
standards and work practice standards for specialty coatings are 58
tons of HAP per year. As noted above, we are proposing that the MACT
standard, prior to the implementation of these proposed standards for
specialty coatings, provides an ample margin of safety to protect
public health. Therefore, we maintain that, after the implementation of
these standards for specialty coatings, the rule will continue to
provide an ample margin of safety to protect public health.
Consequently, based on current information, we do not expect it will be
necessary to conduct another residual risk review under CAA section
112(f) for this source category 8 years following promulgation of new
emission limits and equipment and work practice standards for specialty
coatings, merely due to the addition of these MACT requirements. While
our decisions on risk acceptability and ample margin of safety are
supported even in the absence of these reductions for specialty
coatings, if we finalize the proposed requirements for these sources,
they would further strengthen our conclusions that risk is acceptable
with an ample margin of safety to protect public health.
Although we did not identify any new technologies, other than for
specialty coatings application operations, to reduce risk for this
source category, we are specifically requesting comment on whether
there are additional control measures that may be able to reduce risks
from the source category. We request any information on potential
emission reductions of such measures, as well the cost and health
impacts of
[[Page 8416]]
such reductions to the extent they are known.
3. Adverse Environmental Effects
Based on the results of our environmental risk screening
assessment, we conclude that there is not an adverse environmental
effect as a result of HAP emissions from the Aerospace Manufacturing
and Rework Facilities source category. We are proposing that it is not
necessary to set a more stringent standard to prevent, taking into
consideration costs, energy, safety and other relevant factors, an
adverse environmental effect.
D. What are the results and proposed decisions based on our technology
review?
As described in section III.C of this preamble, our technology
review focused on identifying developments in practices, processes and
control technologies for the Aerospace Manufacturing and Rework
Facilities source category. The EPA reviewed various information
sources regarding emission sources that are currently regulated by the
Aerospace NESHAP, which include primer and topcoat application
operations, maskant application operations, cleaning operations,
chemical and blast depainting operations and waste storage and handling
operations.
For the technology review, we conducted a search of the EPA's RACT/
BACT/LAER Clearinghouse (RBLC) and regulatory actions (MACT standards,
area sources standards and residual risk standards) subsequent to
promulgation of the 1995 Aerospace NESHAP.\32\ We reviewed Washington
State's records of Prevention of Significant Deterioration (PSD)
permits. Further, we considered numerous relevant regional and state
regulations (e.g., California, Missouri, Delaware and Arizona), the
Ozone Transport Commission serving the Northeastern United States and
state implementation plans. We reviewed the database of responses to
the 2011 ICR to determine the technologies and practices reported by
industry.
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\32\ See the EPA's ``Coatings and Composites Coordinated Rule
Development'' Web page at https://www.epa.gov/ttnatw01/coat/coat.html
for a full list of surface coating-related NESHAP, and links to Web
pages specific to each surface coating NESHAP.
---------------------------------------------------------------------------
We reviewed these sources for information on add-on control
technologies, other process equipment, work practices and procedures
and process changes or pollution prevention alternatives that were not
considered during development of the Aerospace NESHAP. We also looked
for information on improvements in add-on control technology, other
process equipment, work practices and procedures and process changes or
pollution prevention alternatives that have occurred since development
of the Aerospace NESHAP. Regarding process changes or pollution
prevention alternatives, we searched for advancements in the use of
low-HAP coatings and solvents, advancements in the use of high solids
coatings and the adoption of lower VOC content limits for coatings and
solvents.
The following sections summarize our technology review results for
each of these emission sources.
1. Primer and Topcoat Application Operations
As defined in the Aerospace NESHAP (see 40 CFR 63.742), a coating
is a material that is applied to the surface of an aerospace vehicle or
component to form a decorative or functional solid film, or the solid
film itself. A primer is the first layer and any subsequent layers of
coating prior to the topcoat and is typically used for corrosion
prevention, protection from the environment, functional fluid
resistance and adhesion of subsequent coatings. A topcoat is a coating
that is applied over one or more layers of a primer for appearance,
identification, camouflage or protection. Specialty coatings are not
included in the categories of primers or topcoats currently subject to
regulation under 40 CFR 63.745.
Most aerospace coatings contain a mixture of organic solvents that
may be HAP, and also inorganic pigments, such as various metal
compounds, which may also be HAP. The organic HAP emissions from the
application of primers and topcoats occur from the evaporation of
organic solvents during mixing, application and drying. Emissions of
inorganic HAP from spray-applied coating operations, typically metal
compounds (e.g., chromium, cadmium compounds), occur when coating
particles do not adhere to the surface being coated (i.e., overspray).
The organic and inorganic emissions from coating application occur in
large open areas, such as hangars or in partially or fully enclosed
spaces, such as within spray booths.
The existing Aerospace NESHAP requires the following organic HAP
and VOC content limits for uncontrolled primers and topcoats (40 CFR
63.745(c)):
Primers: 2.9 lb/gal (less water) as applied; or 4.5 lb/gal
(less water) as applied for general aviation rework facilities, or 5.4
lb/gal (less water) as applied, to large commercial aircraft components
(parts or assemblies) or fully assembled, large commercial aircraft.
Topcoats: 3.5 lb/gal (less water) as applied; or 4.5 lb/
gal (less water) as applied for general aviation rework facilities.
Alternatively, a control system can be used to capture and control
organic HAP and VOC emissions from the primer or topcoat application
operations. The system must achieve an overall control efficiency of 81
percent of organic HAP and VOC emissions (40 CFR 63.745(d)).
In addition, the Aerospace NESHAP requires the use of one of the
following coating application techniques (40 CFR 63.745(f)):
Flow/curtain coat application.
Dip coat application.
Roll coating.
Brush coating.
Cotton-tipped swab application.
Electrodeposition (dip) coating.
High volume low pressure (HVLP) spraying.
Electrostatic spray application.
Other coating application methods that achieve emission
reductions equivalent to HVLP or electrostatic spray application
methods.
The Aerospace NESHAP also includes operating requirements for the
application of primers or topcoats that contain inorganic HAP,
including control of spray booth exhaust streams with either
particulate filters or waterwash spray booths (40 CFR 63.745(g)).
Based on the technology review for primers and topcoats, we did not
identify any practices, processes or control technologies beyond those
already required by the Aerospace NESHAP. A brief summary of the EPA's
findings in conducting its RTR review of primer and topcoat application
operations follows. For a detailed discussion of the EPA's findings,
refer to the memorandum, Technology Review for Primer and Topcoat
Application Operations in the Aerospace Source Category, January 2015,
available in the docket for this action.
In reviewing add-on control technologies or other equipment and
work practices and procedures, we did not identify any add-on control
technologies, other equipment or work practices and procedures that had
not previously been considered during development of the Aerospace
NESHAP, nor did we identify any developments in the same since the
promulgation of the NESHAP.
Based on our search of the RBLC, we did not find any more stringent
requirements. We identified one facility
[[Page 8417]]
in Washington State, for which a Best Achievable Control Technology
(BACT) analysis was completed in September 2014, for constructing new
buildings needed for producing new models of large commercial
airplanes, including the building and surface coating of composite
aircraft wings. The surface coating operations on these aircraft wings
would involve the use of primers and topcoats that are subject to the
limits in 40 CFR 63.745. The BACT analysis concluded that there are no
demonstrations of add-on controls at facilities performing surface
coating comparable to large commercial aircraft wing components. The
analysis also concluded that add-on controls would not be cost
effective for surface coating of large components, such as wings, much
less fully assembled large commercial aircraft.
In reviewing improvements in add-on control technologies or other
equipment that had previously been considered during development of the
Aerospace NESHAP, specifically in conducting a technology review of the
wood manufacturing industry, we found that the Wood Furniture
Manufacturing NESHAP, 40 CFR part 63, subpart JJ, requires the use of
high-efficiency spray guns (e.g., airless spraying, air assisted
airless spraying, electrostatic spraying and HVLP spray guns) and
prevents the use of conventional spray guns. Although the Aerospace
NESHAP does not specifically prohibit the use of conventional spray
methods, it does specify that only spray application methods that are
equivalent to HVLP or electrostatic spray application methods may be
used. Because conventional spray guns can be used only if they can
achieve the same efficiency as HVLP or electrostatic spray application
methods, the Aerospace NESHAP and the Wood Furniture Manufacturing
NESHAP are essentially equivalent. No other new developments in add-on
control technologies or other equipment were found.
The EPA reviewed the 2011 ICR data for advancements in the use of
low-HAP liquid primers and topcoats as process changes and pollution
prevention alternatives that could be transferred to and used in this
source category and that were not identified and considered during
development of the Aerospace NESHAP. In this review, we found some
facilities with weighted-average HAP content values below the HAP and
VOC content limits for primers and topcoats in the Aerospace NESHAP.
However, the data collected by the ICR cannot be compared directly with
the HAP and VOC content limits in the Aerospace NESHAP because the
NESHAP limits are based on grams of HAP per liter of coating, less
water. The ICR asked for readily available data, such as data from
product sheets and material safety data sheets, which did not provide
data on the water content of the coatings. As a result, we cannot
accurately convert the reported HAP contents from the ICR to the same
basis as in the Aerospace NESHAP. Moreover, we believe that if the
coatings in the ICR contained water and the water content of the
coatings is removed, then the corrected HAP content of the coatings
would increase and the apparent difference between the ICR data and the
NESHAP limits would be reduced.
Finally, many of the currently used coatings have already been
reformulated to meet the current MACT HAP content limits. Manufacturers
of aerospace vehicles are constrained to using certain types of primers
and topcoats based on the market segment for which the coating is
intended (i.e., military original equipment manufacturer (OEM),
military rework, commercial OEM or commercial rework) and the unique
circumstances and design considerations within each market segment. In
addition to being regulated by the Aerospace NESHAP, aerospace vehicle
manufacturing and rework operations are also regulated by the Federal
Aviation Administration (FAA), the Department of Defense and specific
customer requirements. As outlined in the EPA's 1998 promulgation of
amendments to the Aerospace NESHAP,\33\ affected sources must comply
with FAA Airworthiness Directives (AD) that can potentially require the
use of chemicals containing HAP, and affected sources may have to
obtain alternative means of compliance for AD to allow for the
substitution of non-HAP materials. These multiple regulations can
result in lengthy processes for qualifying new paint systems.
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\33\ 63 FR 46525, September 1, 1998.
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Based on a finding of no new developments in practices, processes
and control technologies in the technology review for primer and
topcoat application operations, we are not proposing to revise the
Aerospace NESHAP HAP and VOC content limit requirements for primer and
topcoat application operations pursuant to CAA section 112(d)(6). For
further discussion of the technology review results, refer to the
memorandum, Technology Review for Primer and Topcoat Application
Operations in the Aerospace Source Category, January 2015, available in
the docket for this action.
2. Chemical Milling Maskant Application Operations
In the process of chemical milling, an etchant solution is used to
chemically reduce the thickness of selected areas of metal parts. The
process is typically used when the size or shape of the part precludes
mechanical milling or when chemical milling is advantageous due to
shorter processing time or its batch capability. Before chemical
milling, a maskant is applied to the part, allowed to cure and is then
removed from selected areas of the part where metal is to be removed by
the etchant. The maskant remaining on the part protects those areas
from the etchant. Maskants are applied by brushing, dipping, spraying
or flow coating. Organic HAP emissions occur through evaporation of the
solvent in the maskant, typically toluene, xylene or perchloroethylene,
as the maskant is applied and while it cures.
There are two subcategories of chemical milling maskants in the
Aerospace NESHAP. Type I maskants are used with chemical milling
etchants that contain dissolved sulfur and no amines, and Type II
maskants are used with etchants that are strong sodium hydroxide
solutions containing amines. The Aerospace NESHAP requires the
following organic HAP and VOC content limits for uncontrolled chemical
milling maskants (40 CFR 63.747(c)):
Type I: 5.2 pounds organic HAP per gallon (622 g/L) less
water, as applied.
Type II: 1.3 pounds of organic HAP per gallon (160 g/L)
less water, as applied.
These requirements do not apply to touch-up of scratched surfaces
or damaged maskant and touch-up of trimmed edges. Alternatively, a
control system can be used to capture and control emissions from the
maskant application operation. The system must achieve an overall
control efficiency of 81 percent (40 CFR 63.747(d)).
Based on the technology review for chemical milling maskants, we
did not identify any add-on control technologies, other equipment or
work practices and procedures that had not previously been considered
during development of the Aerospace NESHAP. Additionally, we did not
identify any improvements that could be transferred to this source
category. In our search of the RBLC, we also did not find any more
stringent requirements. We did find that some California air quality
management districts require more stringent VOC content limits than
those in the Aerospace NESHAP and have higher overall minimum control
requirements for the use of add-on control technology.
[[Page 8418]]
However, the EPA did not find any chemical milling maskant application
operations located in these two districts that are subject to these
more stringent limits.
Based on a finding of no new developments in practices, processes
and control technologies in this technology review, we are not
proposing revisions to the Aerospace NESHAP for chemical milling
maskant application operations pursuant to CAA section 112(d)(6). Refer
to the memorandum, Technology Review for Chemical Milling Maskant
Application Operations in the Aerospace Source Category, January 2015,
available in the docket for this action, for more a more detailed
description of the technology review results.
3. Cleaning Operations
At Aerospace Manufacturing and Rework Facilities, cleaning
operations are used at essentially every processing step of aerospace
surface coating, from preparing surfaces to be coated to cleaning the
coating application equipment. The cleaning operations regulated by the
current Aerospace NESHAP include hand-wipe cleaning, spray gun cleaning
and flush cleaning, as well as housekeeping measures for storage,
handling and transfer of cleaning solvents and solvent-laden materials.
The liquid cleaning solutions used in cleaning operations for the
aerospace industry contain organic solvents, and some of these organic
solvents are HAP. Organic HAP emissions from the cleaning operations
are often fugitive in nature, resulting from the evaporation of the
volatile portion of the cleaning solvent in large open areas, such as
hangars. They may also be emitted from stacks when the solvents are
used in partially or fully enclosed spray booths that are ventilated
through stacks.
The current Aerospace NESHAP requires that hand-wipe and flush
cleaning solvents meet certain composition requirements, or that the
cleaning solvents have a composite vapor pressure of no more than 45 mm
Hg (24.1 inches water) (40 CFR 63.744(b) and (d)). The NESHAP specifies
work practice standards for spray gun cleaning (e.g., cleaning a spray
gun in an enclosed gun cleaning system) and flush cleaning operations
(e.g., for flush cleaning events, empty used cleaning solvent into an
enclosed container) (40 CFR 63.744(c) and (d)). Work practice measures
are also specified for the storage and handling of solvents and
solvent-laden materials (e.g., solvent-laden cloth, paper or other
absorbent materials) (40 CFR 63.744(a)).
Based on the technology review for cleaning operations, we did not
identify any practices, processes or control technologies beyond those
already required by the Aerospace NESHAP that could be transferred to
the source category. A brief summary of the EPA's findings in
conducting its RTR review of cleaning operations follows. For a
detailed discussion of the EPA's findings, refer to the memorandum,
Technology Review for Cleaning Operations in the Aerospace Source
Category, January 2015, available in the docket for this action.
In the technology review, we did not identify any improvements in
add-on control technologies, other equipment or work practices and
procedures since promulgation of the Aerospace NESHAP. The EPA
identified one aerospace manufacturing and rework facility that routes
the air flow from a spray booth to a carbon adsorption control device
when performing spray gun cleaning and residual spray gun hand-wipe
cleaning. We found that this was the same spray booth in which surface
coating is performed, and it is not a spray booth dedicated to spray
gun cleaning. Based on the results of the responses to the EPA's 2011
information collection survey for other facilities, the EPA concluded
that this practice could not be applied to the source category without
impacting facility operations. First, very few facilities have carbon
adsorbers controlling emissions from spray booths. Second, it is not
always practical to move the spray gun cleaning operations into a spray
booth without affecting the surface coating operations in that spray
booth because of space limitations within the booth.
The EPA also identified one aerospace manufacturing and rework
facility that, for certain cleaning operations, uses a non-HAP solvent
blend that has a vapor pressure of 36 mm Hg for certain cleaning
operations; the facility does not use this solvent for all cleaning
operations. The use of non-HAP cleaning solvent is already a compliance
option that was considered in the development of the Aerospace NESHAP
and is included in 40 CFR 63.744.
Based on a finding of no new developments in practices, processes
and control technologies in the technology review, we are not proposing
any revisions to the Aerospace NESHAP standard requirements for
cleaning operations pursuant to CAA section 112(d)(6). For further
discussion of the technology review results, refer to the memorandum,
Technology Review for Cleaning Operations in the Aerospace Source
Category, January 2015, available in the docket for this action.
4. Chemical and Dry Media Blasting Depainting Operations
At Aerospace Manufacturing and Rework Facilities, chemical and dry
media blasting depainting operations remove unwanted or old surface
coatings (e.g., primers, topcoats and specialty coatings) to prepare
the surface for painting. As defined in the Aerospace NESHAP, a
depainting operation means the use of a chemical agent, media blasting
or any other technique to remove permanent coatings from the outer
surface of an aerospace vehicle or components, excluding hand and
mechanical sanding or other non-chemical removal processes that do not
involve blast media or other mechanisms that would result in airborne
particle movement at high velocity. The depainting operation includes
washing of the aerospace vehicle or component to remove residual
stripper, media or coating residue. Depainting is most often done in
the rework of existing aircraft, but may also be done in limited
circumstances in the manufacture of new aircraft.
The liquid chemical agents (i.e., strippers) used to remove
permanent coatings in the aerospace industry contain organic solvents.
Organic HAP emissions from strippers occur from the evaporation of the
chemical stripper during mixing, application and possibly during
washing of the vehicle or component to remove residual stripper. The
organic emissions from depainting operations that occur within a booth
or hangar are typically captured and exhausted through a stack,
although some emissions may be fugitive in nature (e.g., open
containers of stripper).
Inorganic HAP, typically metal compounds (e.g., compounds of lead,
chromium or cadmium), can be emitted during dry media blasting if these
compounds are present in the paint layer that is being removed. These
inorganic HAP would be emitted as particulate matter as the dry media
blasting removes the existing coating through abrasion.
The Aerospace NESHAP restricts facilities to using organic HAP-
containing chemical strippers for only spot stripping and decal
removal. The amount of stripper used for spot stripping and decal
removal is limited to no more than 26 gallons of HAP-containing
chemical stripper (or alternatively 190 pounds of organic HAP) for each
commercial aircraft, and 50 gallons (or 365 pounds of organic HAP) for
each military aircraft. As an alternative, facilities may use controls
for organic HAP emissions from
[[Page 8419]]
chemical depainting, and emissions must be reduced by 81 percent for
controls installed before the effective date, and by 95 percent for
controls installed on or after the effective date (40 CFR 63.746(b)(1)
through (3) and (c)).
For non-chemical depainting operations that generate inorganic HAP
emissions from dry media blasting, the operation must be performed in
an enclosed area or in a closed cycle depainting system and the air
stream from the operation must pass through a dry filter system meeting
a minimum efficiency specified in the rule, through a baghouse or
through a waterwash system before being released to the atmosphere (40
CFR 63.746(b)(4)).
Based on the technology review for depainting operations, we did
not identify any practices, processes or control technologies that were
not already required by the Aerospace NESHAP or considered in its
development, nor did we identify any improvements to those practices,
processes or control technologies that could be transferred and applied
to this source category. A brief summary of the EPA's findings in
conducting the RTR review of chemical and dry media blast depainting
operations follows. For a detailed discussion of the EPA's findings,
refer to the memorandum, Technology Review for Depainting Operations in
the Aerospace Source Category, January 2015, available in the docket
for this action.
In reviewing Washington State's records of permits for Aerospace
Manufacturing and Rework Facilities, we identified a 2013 PSD permit
amendment that requires the VOC vapor pressure of cleaning solvents and
chemical strippers used in depainting operations to be less than 45 mm
Hg. The Aerospace NESHAP does not prescribe vapor pressure limits to
chemical depainting strippers, but instead has capture and control and
volume usage limits for chemical depainting operations that use HAP-
containing chemical strippers. Otherwise, facilities must use non-HAP
chemical strippers. Therefore, we believe that the Aerospace NESHAP is
at least as stringent as the Washington State PSD permit requirements.
Based on a finding of no new developments in practices, processes
and control technologies in the technology review, we are not proposing
to revise the Aerospace NESHAP standard requirements for chemical or
dry media blast depainting operations pursuant to CAA section
112(d)(6). For further discussion of the technology review results,
refer to the memorandum, Technology Review for Depainting Operations in
the Aerospace Source Category, January 2015, available in the docket
for this action.
5. Waste Storage and Handling Operations
At Aerospace Manufacturing and Rework Facilities, waste is produced
primarily from cleaning, coating and depainting operations. Cleaning
operations produce solvent-laden cloth and paper and spent solvent
which can emit organic HAP from the evaporation of the solvents.
Coating operations produce waste paint and waste solvent that also emit
organic HAP through evaporation.
Depainting operations can produce either a liquid or solid waste
stream depending on the type of process used. Chemical depainting
processes produce a waste sludge that consists of the stripper solution
and paint residue. Emissions occur from the evaporation of the solvent
from the stripper solution in the waste sludge.
Blast depainting processes produce a solid waste stream that
consists of paint chips and particles and spent blasting media.
Emissions do not directly occur from this waste stream, although
particulate emissions are generated during the blasting process.
The requirements for waste storage and handling in the Aerospace
NESHAP apply to each waste storage and handling operation, which is
defined as the total of all waste handling and storage at the facility.
In 40 CFR 63.748, the Aerospace NESHAP requires that all waste must be
handled and transferred to or from containers, tanks, vats, vessels and
piping systems in such a manner that spills are minimized.
Because the EPA did not want to create possible conflicts over the
handling of waste between the Aerospace NESHAP and regulations under
the Resource Conservation and Recovery Act (RCRA) of 1976 (Pub. L. 94-
580), as implemented by 40 CFR parts 260 and 261, the Aerospace NESHAP
specifically exempted wastes covered under the RCRA regulations.\34\
Per 40 CFR 63.741(e), all wastes that are determined to be hazardous
wastes under RCRA as implemented by 40 CFR parts 260 and 261, and that
are subject to RCRA requirements as implemented in 40 CFR parts 262
through 268, are exempt from the requirements of the Aerospace NESHAP.
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\34\ See the preamble to the proposed rule, 59 FR 29216, June 6,
1994.
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The practical effect of the provisions in 40 CFR 63.741(e) is that
all HAP-containing wastes generated by aerospace manufacturing and
rework operations are subject to RCRA and are exempt from the
requirements of 40 CFR 63.748. Because all of these HAP-containing
wastes are covered under RCRA and exempt from 40 CFR 63.748, there is
no need to do a technology review for the standards for handling and
storage of waste.
E. What other actions are we proposing?
In addition to the proposed actions described above, we are
proposing additional revisions. As stated previously in this preamble,
the United States Court of Appeals for the District of Columbia Circuit
found that the EPA had erred in establishing emissions standards for
sources of HAP in the NESHAP for Brick and Structural Clay Products
Manufacturing and Clay Ceramics Manufacturing, 67 FR 26690 (May 16,
2003), and consequently vacated the rules.\35\ Among other things, the
court found EPA erred by failing to regulate processes that emitted
HAP, in some instances by establishing a MACT floor of ``no control.''
In this action we are proposing to correct the same error in the
Aerospace NESHAP by proposing to remove the exemption for specialty
coatings found at 40 CFR 63.741(f) and instead add limits for specialty
coatings (including adhesives, adhesive bonding primers and sealants).
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\35\ Sierra Club v. EPA, 479 F. 3d 875 (D.C. Cir. March 13,
2007).
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1. Specialty Coating Application
At Aerospace Manufacturing and Rework Facilities, specialty
coatings are those coatings that have additional performance criteria
for specific applications that are beyond the criteria for primers,
topcoats and self-priming topcoats, although specialty coatings may
still meet the definition of a primer or topcoat. These additional
performance criteria may include, for example, temperature or fire
resistance, substrate compatibility, antireflection, temporary
protection or marking, sealant properties, adhesive properties,
electrical insulation, lubrication or enhanced corrosion protection (40
CFR 63.742).
Specialty coatings contain a mixture of organic solvents and/or
inorganic HAP. The organic HAP emissions from the application of
specialty coatings occur from the evaporation of organic solvents
during mixing, application and drying. Emissions of inorganic HAP from
spray-applied coating operations, typically metal compounds (e.g.,
chromium, cadmium compounds), occur when particles do not adhere to the
surface being coated (i.e.,
[[Page 8420]]
overspray). The organic and inorganic emissions from coating
application operations occur in large open areas, such as hangars or
partially or fully enclosed spaces, such as within spray booths.
The current Aerospace NESHAP explicitly excludes specialty coatings
from meeting any control requirements, as specified in 40 CFR 63.741(f)
and in 40 CFR 63.742 (i.e., the definitions for ``exterior primer,''
``primer,'' and ``topcoat''). Appendix A of the Aerospace NESHAP
defines 59 separate categories of specialty coatings.
Although the EPA did not include emission limitations for specialty
coatings in the Aerospace NESHAP finalized in 1995 or in any subsequent
amendments, the EPA included VOC content limits for the 59 categories
of specialty coatings in the 1997 Aerospace CTG. The Aerospace CTG is
intended to provide state and local air pollution control authorities
with an information base, recommended emissions limitations and
monitoring, recordkeeping and reporting requirements for proceeding
with their analyses of reasonably available control technology (RACT)
for their own regulations to reduce VOC emissions from aerospace
surface coating operations. The Aerospace CTG includes presumptive VOC
limits for specialty coating operations that are based on a review of
the contemporary knowledge and data concerning the technology, impacts
and costs associated with various emission control techniques. During
their development, the specialty coating categories and VOC limits in
the CTG were also subject to a period of public comment and review, and
the final CTG categories and VOC limits were revised after proposal to
reflect the EPA's analysis of those comments on the proposed CTG.
In this action, we are proposing to establish standards for
specialty coatings. Based on a MACT analysis for specialty coatings, we
are proposing to require aerospace manufacturing and rework specialty
coating application operations to achieve organic HAP content limits
that are equivalent to the VOC content limits for specialty coatings
included in the Aerospace CTG. As discussed previously in section
IV.E.1 of this preamble, the Aerospace CTG may be adopted by state and
local agencies in nonattainment areas to assist them in meeting their
state implementation plan requirements. Of the 109 facilities that
reported the use of specialty coatings, 35 are in nonattainment areas
and likely currently complying with the specialty coating limits in the
Aerospace CTG. The remaining facilities would need to take action to
comply with the specialty coating application operations limits.
In the MACT analysis for specialty coatings, the EPA considered
data provided in response to a comprehensive information collection
request (ICR) sent out in February 2011 and consulted the EPA's RACT/
BACT/LAER Clearinghouse, the California Statewide Best Available
Control Technology (BACT) Clearinghouse and regional and state
regulations for sources of data on control technologies and
limitations. We reviewed state rules to compare the VOC limits in those
rules to the VOC limits in the Aerospace CTG. This review of state
rules was in addition to a review of the database of responses to the
2011 ICR and the RBLC for information on add-on control technology or
other equipment, work practices and procedures and process changes or
pollution prevention alternatives not identified and considered during
development of the Aerospace CTG, or improvements in the same since the
CTG development. A brief summary of the EPA's findings in conducting
its MACT analysis of specialty coating application operations follows.
For a detailed discussion of the EPA's findings, refer to the
memorandum, Maximum Achievable Control Technology for Specialty Coating
Operations in the Aerospace Source Category, January 2015, available in
the docket for this action.
For specialty coatings, where there were sufficient data, the EPA
compared the emissions for the best performing coatings with the
Aerospace CTG limits. The results of this comparison showed that the
CTG VOC limits were equivalent in performance to the best performing
specialty coating. Therefore, we determined that the current Aerospace
CTG limits represent MACT for specialty coatings.
Based on the results of the MACT analysis, we determined that the
VOC limits in the Aerospace CTG for specialty coatings are currently
being achieved by about half of all operating sources subject to the
Aerospace NESHAP. The facilities complying with the CTG limits for
specialty coatings are located in ozone non-attainment areas where
state VOC rules have been developed based on the Aerospace CTG. From
our review of industry responses to the 2011 ICR, we determined that
some facilities complying with these state VOC limits employ use of
add-on control devices to reduce organic HAP emissions (i.e., thermal
oxidizers and carbon adsorbers); however, these add-on controls are not
widely used in the source category. Other facilities achieve equivalent
emission reductions without add-on controls by using coatings that meet
the VOC content limits.
Based on our review of state and regional regulations for specialty
coating operations in the aerospace industry, we identified several
cases in which limits are specified for certain specialty coating
categories that are lower than the VOC content limits for the same
specialty coating categories in the Aerospace CTG. These differences
generally affect about one-quarter of the specialty coating categories
(although each state or regional regulation may differ from the CTG in
only a handful of categories), and the limits differ by less than 200
grams VOC per liter of coating. However, these state and regional rules
and the Aerospace CTG differ in certain ways, such that the lower VOC
limits in the state and regional rules do not represent a more
stringent limit as compared to the Aerospace CTG.
First, in many cases where a state rule has a lower VOC limit than
the CTG, the state rule has also added coating categories with VOC
limits equal to or higher than the CTG limits. For example, one state
rule has a lower limit for fuel tank coatings, but has an additional
category for ``rapid cure'' fuel tank coatings that is the same as the
CTG VOC limit.
Second, not all categories of specialty coatings are used at all
Aerospace Manufacturing and Rework Facilities. For the specialty
categories with more stringent VOC limits, the EPA does not have data
to confirm that facilities exist in those jurisdictions that are using
those coatings and actually have to comply with the more stringent VOC
limits. These data on facilities actually using coatings subject to
these more stringent limits would be needed to confirm that these more
stringent limits constitute the MACT floor according to section
112(d)(3) of the CAA.
Finally, many of the areas with more stringent VOC limits than in
the CTG have climates that are warmer and drier than in most other
parts of the United States, and this type of climate is more conducive
to the use of low-VOC coatings because it helps promote expeditious
curing of the coatings under ambient conditions. In cooler and more
humid areas, the coatings require the use of a solvent carrier and/or
thermal curing. The Aerospace NESHAP and CTG, on the other hand, must
establish HAP and VOC limits that are applicable across the United
States. It is not practical to establish MACT limits for coatings based
on regional climate differences for this source category.
[[Page 8421]]
Based on the issues noted above, the EPA concludes that the noted
differences between the state and regional rules and the Aerospace CTG
limits do not constitute more stringent limits compared to those in the
Aerospace CTG. The EPA does not have sufficient data to determine
whether these differences in VOC limits, compared to the limits in the
Aerospace CTG, actually constitute MACT. Therefore, the EPA is
specifically soliciting comment and additional data on the differences
noted between state and regional rules and the aerospace CTG.
Based on its analysis, the EPA is proposing the MACT floor for
specialty coatings to be organic HAP content limits equal to the VOC
limits specified in the Aerospace CTG for specialty coatings.
Additionally, the low-volume exemption provisions in the current
Aerospace NESHAP for primers, topcoats and chemical milling maskants
may be used for specialty coatings. The EPA has not identified any
options more stringent than the MACT floor as documented in the review
of specialty coatings discussed earlier in this section, so the
proposed organic HAP content limits are equal to the MACT floor VOC
content limits. The EPA is proposing this MACT floor based on the fact
that these VOC limits are currently being achieved by at least 12
percent of the operating facilities in a total population of 109
operating aerospace and rework facilities that reported using specialty
coatings in the 2011 ICR. For more information on the MACT floor
analysis, please refer to the memorandum, Maximum Achievable Control
Technology for Specialty Coating Operations in the Aerospace Source
Category, January 2015, available in the docket for this action.
In reviewing the state and district VOC rules, the EPA determined
that the aerospace surface coating rules in many of the California
district rules, in addition to the requirement to meet VOC limits,
require that all spray-applied coating operations use high-efficiency
application equipment (i.e., HVLP, electrostatic spray or an
equivalent). This requirement is more stringent than the model rule
found in the Aerospace CTG, which exempts specialty coatings from the
requirement to use high-efficiency application equipment. The
California rules examined by the EPA require the use of high-efficiency
application equipment for all spray applied coatings, unless an add-on
control system was used, or certain other exemptions apply. Other state
rules that follow the CTG require high-efficiency application methods
only for primer and topcoat application operations. The facilities
located in California that are required to use high-efficiency
application equipment for specialty coatings constitute the MACT floor
for the application of these coatings. This determination is based on
the fact that at least 11 facilities in California's air pollution
control districts are currently subject to district rules that require
high-efficiency application equipment for all coating operations,
including specialty coatings. Therefore, the EPA is proposing that
specialty coatings be subject to the same application requirements in
40 CFR 63.745(f) as primers and topcoats. Compared to conventional
spray application methods, high-efficiency application methods, such as
HVLP spray guns or electrostatic deposition, can achieve HAP and VOC
emission reductions because of reduced coating consumption that results
from reduced coating overspray. The EPA has not identified any control
options more stringent than the use of high-efficiency application
methods for spray-applied coating operations.
In our review of the RBLC, we did not identify any control options
for aerospace specialty surface coating operations that were not
already reflected in the VOC content limits in the Aerospace CTG.
However, we identified one facility in the state of Washington for
which a BACT analysis was completed in September 2014, for constructing
new buildings needed for producing new models of large commercial
airplanes, including the building and surface coating of composite
aircraft wings. The BACT analysis described the facility as currently
using HVLP spraying and electrostatic airless and modified high-
efficiency air-assisted airless spray equipment in all spray applied
surface coating operations. The BACT analysis concluded that there were
no demonstrations of add-on controls at facilities performing surface
coating comparable to large commercial aircraft wing components.
In our review of Washington State's record of permits, we
determined that the current PSD permit for this facility identified
BACT for VOC from coating operations to be the equivalent of complying
with ``all applicable VOC emission standards of the Aerospace NESHAP.''
The PSD permit for the facility did not consider add-on control
technologies to be BACT after taking into account energy, environmental
and economic impacts. Based on this information from the RBLC and the
Washington State BACT analysis, we determined that add-on control
techniques would not be MACT for specialty coating application
operations for the aerospace industry.
Instead, MACT is being proposed as the use of low-HAP coatings
(with HAP content limits equal to the VOC content limits in the
Aerospace CTG) and high-efficiency application methods for spray-
applied coating operations. As the EPA did with primers and top coats
in the current NESHAP, the EPA is proposing to use VOC limits that are
currently in effect as the basis for proposed organic HAP limits.
The EPA is also proposing to establish MACT to limit emissions of
inorganic HAP from spray-applied specialty coatings that contain
inorganic HAP. The predominant method used to control inorganic HAP
emissions from all spray-applied coating operations (including
specialty coatings) is the use of a spray booth with a particulate
filter, which generally achieves a high (i.e., greater than 99 percent)
control efficiency. The Aerospace NESHAP currently requires the use of
spray booths with filters meeting minimum efficiency requirements for
the spray application of primers and topcoats that contain inorganic
HAP. Based on the results of the 2011 ICR, the EPA has determined that
the vast majority of spray-applied specialty coatings are currently
applied in spray booths. It is likely that these specialty coatings are
applied in the same spray booths as primers and topcoats, or at least
in spray booths that are very similar to those used for primer and
topcoat operations. Therefore, the same inorganic HAP emission
limitations that are applied to primer and topcoat operations should
also be applicable to specialty coating operations, and the EPA is
proposing to extend these limitations to specialty coating operations.
The EPA has not identified any control options more stringent than the
use of spray booths with high-efficiency filters to control inorganic
HAP emissions from spray-applied coating operations.
In summary, the EPA is proposing to add a requirement to the
Aerospace NESHAP that Aerospace Manufacturing and Rework Facilities
comply with organic HAP or VOC content limits for specialty coatings
that are equal to the VOC content limits specified in the Aerospace
CTG. The EPA is also proposing that specialty coating application
operations be subject to the same application equipment requirements in
40 CFR 63.745(f), and the standards for inorganic HAP emissions in 40
CFR 63.745(g) that apply to primer and topcoat application operations.
We request comment on our analysis and supporting info on any
[[Page 8422]]
other practices that may be used to limit emissions from specialty
coatings.
The EPA believes that the proposed HAP and VOC content limits for
specialty coatings are achievable because they are based on the VOC
content limits in the Aerospace CTG, which have been adopted in many
state and local VOC rules. In the development of these proposed
amendments, the EPA made repeated efforts to reach out to and solicit
input from aerospace manufacturers on the coating performance and
reformulation challenges, if any, presented by complying with specialty
coating limits based on the current CTG. However, the information
presented so far has been only anecdotal, and not for the full range of
specialty coating categories in the CTG.
Therefore, the EPA is specifically soliciting comment and
additional data on any changes needed to the definitions of specialty
coating categories and the proposed organic HAP and VOC limits. The EPA
will consider comments on changes to the definitions of specialty
coating categories that may be needed to clarify the scope of each of
the individual specialized coating categories, based on industry
experience, including complying with those categories in rules derived
from the Aerospace CTG. The EPA will consider data and information on
specific cases (not just general examples) of specialty coatings that
could not meet the current definitions of the specialty coating
categories or the proposed organic HAP or VOC content limits for those
categories. Please provide with your comments information on the
following: The annual volume of the coating used, the container size,
the container type, the military specification or FAA AD that applies,
the specialty category that applies, documentation of the organic HAP
or VOC content of the coating and suggested changes to category
definitions (if applicable and feasible) that would include the coating
in a more appropriate category with a higher HAP or VOC limit. The EPA
will consider any submitted data that supports a comment that a
specific coating cannot meet the proposed organic HAP or VOC content
limit for a particular specialty coating category.
The estimated costs, emission reductions, other (non-air)
environmental impacts and energy impacts associated with the proposed
regulation of specialty coatings are presented in section V of this
preamble.
2. Electronic Reporting Requirements
In this proposal, the EPA is describing a process to increase the
ease and efficiency of performance test data submittal while improving
data accessibility. Specifically, the EPA is proposing that owners and
operators of Aerospace Manufacturing and Rework Facilities submit
electronic copies of required performance test and performance
evaluation reports by direct computer-to-computer electronic transfer
using EPA-provided software. The direct computer-to-computer electronic
transfer is accomplished through the EPA's Central Data Exchange (CDX)
using the Compliance and Emissions Data Reporting Interface (CEDRI).
The CDX is the EPA's portal for submittal of electronic data. The EPA-
provided software is called the Electronic Reporting Tool (ERT), which
is used to generate electronic reports of performance tests and
evaluations. The ERT generates an electronic report package which will
be submitted using the CEDRI. The submitted report package will be
stored in the CDX archive (the official copy of record) and the EPA's
public database called WebFIRE. The WebFIRE database was constructed to
store performance test data for use in developing emissions factors.
All stakeholders would have access to all reports and data in WebFIRE
and accessing these reports and data will be very straightforward and
easy (see the WebFIRE Report Search and Retrieval link at https://cfpub.epa.gov/webfire/index.cfm?action=fire.searchERTSubmission). A
description of the WebFIRE database is available at https://cfpub.epa.gov/oarweb/index.cfm?action=fire.main. A description of the
ERT and instructions for using ERT can be found at https://www.epa.gov/ttn/chief/ert/ert_tool.html. CEDRI can be accessed through the CDX Web
site (www.epa.gov/cdx).
The proposal to submit performance test data electronically to the
EPA would apply only to those performance tests conducted using test
methods that will be supported by the ERT. The ERT contains a specific
electronic data entry form for most of the commonly used EPA reference
methods. A listing of the pollutants and test methods supported by the
ERT is available at https://www.epa.gov/ttn/chief/ert/. We
believe that industry would benefit from this proposed approach to
electronic data submittal. Specifically, by using this approach,
industry would save time in the performance test submittal process.
Additionally, the standardized format that the ERT uses allows sources
to create a more complete test report resulting in less potential
failure to include all data elements required to be submitted. Also
through this proposal, industry may only need to submit a report once
to meet the requirements of the applicable subpart because stakeholders
can readily access these reports from the WebFIRE database. This also
would benefit industry by cutting back on recordkeeping costs as the
performance test reports that are submitted to the EPA using CEDRI are
no longer required to be retained in hard copy, thereby reducing staff
time needed to coordinate these records. Another benefit to industry is
that, because the EPA would already have performance test data in hand,
industry would be subject to fewer or less substantial data collection
requests from EPA in conjunction with required future residual risk
assessments or technology reviews. This would result in a decrease in
industry staff time needed to respond to data collection requests.
State, local and tribal air pollution control agencies (S/L/Ts) may
also benefit from having electronic versions of the reports they are
now receiving. For example, S/L/Ts may be able to conduct a more
streamlined and accurate review of electronic data submitted to them.
The ERT would allow for an electronic review process, rather than a
manual data assessment, which will make review and evaluation of the
source provided data and calculations easier and more efficient. In
addition, the public will benefit from electronic reporting of
emissions data because the electronic data will be easier for the
public to access. How the air emissions data are collected, accessed
and reviewed will be more transparent for all stakeholders.
Further, the EPA must have performance test data to conduct
effective reviews of CAA sections 112 and 129 standards, as well as for
many other purposes including compliance determinations, emissions
factor development and annual emissions rate determinations. In
conducting these required reviews, the EPA has found it ineffective and
time consuming, not only for the EPA, but also for regulatory agencies
and source owners and operators, to locate, collect and submit
performance test data because of varied locations for data storage and
varied data storage methods. In recent years, though, stack testing
firms have typically collected performance test data in electronic
format, making it possible to move to an electronic data submittal
system that would increase the ease and efficiency of data submittal
and improve data accessibility.
[[Page 8423]]
One major advantage of the proposed submittal of performance test
data through the ERT is a standardized method to compile and store much
of the documentation required to be reported by this rule. Another
advantage is that the ERT clearly states what testing information would
be required. Another important proposed benefit of submitting these
data to the EPA at the time the source test is conducted is that it
should substantially reduce the effort involved in data collection
activities in the future. When the EPA has performance test data in
hand, the EPA will be able to conduct fewer or less substantial data
collection requests in conjunction with future required residual risk
assessments or technology reviews. This would result in a reduced
burden on both affected facilities (in terms of reduced staff time to
respond to data collection requests) and the EPA (in terms of preparing
and distributing data collection requests and assessing the results).
Finally, another benefit of the proposed data submittal to WebFIRE
electronically is that these data would greatly improve the overall
quality of existing and new emissions factors by supplementing the pool
of emissions test data for establishing emissions factors and by
ensuring that the factors are more representative of current industry
operational procedures. A common complaint heard from industry and
regulators is that emissions factors are outdated or not representative
of a particular source category. With timely receipt and incorporation
of data from most performance tests, the EPA would be able to ensure
that emissions factors, when updated, represent the most current range
of operational practices.
In summary, in addition to supporting regulation development,
control strategy development and other air pollution control
activities, having an electronic database populated with performance
test data would save industry, state, local, tribal agencies and the
EPA significant time, money and effort while also improving the quality
of emissions inventories and, as a result, air quality regulations.
3. Startup, Shutdown and Malfunction Requirements
In its 2008 decision in Sierra Club v. EPA, 551 F.3d 1019 (D.C.
Cir. 2008), cert. denied, 130 S. Ct. 1735 (U.S. 2010), the United
States Court of Appeals for the District of Columbia Circuit vacated
portions of two provisions in the EPA's CAA section 112 regulations
governing the emissions of HAP during periods of SSM. Specifically, the
court vacated the SSM exemption contained in 40 CFR 63.6(f)(1) and
(h)(1), holding that under section 302(k) of the CAA, emissions
standards or limitations must be continuous in nature and that the SSM
exemption violates the CAA's requirement that some section 112
standards apply continuously.
We are proposing the elimination of the SSM exemption in this rule.
Consistent with Sierra Club v. EPA, we are proposing changes so that
standards in this rule would apply at all times. We are also proposing
several revisions to Table 1 to subpart GG of Part 63 (the General
Provisions Applicability Table, hereafter referred to as the ``General
Provisions table'') as explained in more detail below. For example, we
are proposing to eliminate the incorporation of the General Provisions'
requirement that the source develop an SSM plan. We also are proposing
to eliminate and revise certain recordkeeping and reporting
requirements related to the SSM exemption as further described below.
The EPA has attempted to ensure that the provisions we are
proposing to eliminate are inappropriate, unnecessary or redundant in
the absence of the SSM exemption. We are specifically seeking comment
on whether we have successfully done so.
In proposing the standards in this rule, the EPA has taken into
account startup and shutdown periods and, for the reasons explained
below, has not proposed alternate standards for those periods.
Periods of startup, normal operations and shutdown are all
predictable and routine aspects of a source's operations. Malfunctions,
in contrast, are neither predictable nor routine. Instead they are, by
definition sudden, infrequent and not reasonably preventable failures
of emissions control, process or monitoring equipment. The EPA
interprets CAA section 112 as not requiring emissions that occur during
periods of malfunction to be factored into development of CAA section
112 standards. Under section 112, emissions standards for new sources
must be no less stringent than the level ``achieved'' by the best
controlled similar source and, for existing sources, generally must be
no less stringent than the average emission limitation ``achieved'' by
the best performing 12 percent of sources in the category. There is
nothing in section 112 that directs the agency to consider malfunctions
in determining the level ``achieved'' by the best performing sources
when setting emission standards. As the D.C. Circuit has recognized,
the phrase ``average emissions limitation achieved by the best
performing 12 percent of'' sources ``says nothing about how the
performance of the best units is to be calculated.'' Nat'l Ass'n of
Clean Water Agencies v. EPA, 734 F.3d 1115, 1141 (D.C. Cir. 2013).
While the EPA accounts for variability in setting emissions standards,
nothing in CAA section 112 requires the agency to consider malfunctions
as part of that analysis. A malfunction should not be treated in the
same manner as the type of variation in performance that occurs during
routine operations of a source. A malfunction is a failure of the
source to perform in a ``normal or usual manner'' and no statutory
language compels the EPA to consider such events in setting CAA section
112 standards.
Further, accounting for malfunctions in setting emission standards
would be difficult, if not impossible, given the myriad different types
of malfunctions that can occur across all sources in the category and
given the difficulties associated with predicting or accounting for the
frequency, degree and duration of various malfunctions that might
occur. As a result, the performance of units that are malfunctioning is
not ``reasonably'' foreseeable. See, e.g. Sierra Club v. EPA, 167 F.3d
658, 662 (D.C. Cir. 1999) (``The EPA typically has wide latitude in
determining the extent of data-gathering necessary to solve a problem.
We generally defer to an agency's decision to proceed on the basis of
imperfect scientific information, rather than to `invest the resources
to conduct the perfect study.' '') See also, Weyerhaeuser v. Costle,
590 F.2d 1011, 1058 (D.C. Cir. 1978) (``In the nature of things, no
general limit, individual permit, or even any upset provision can
anticipate all upset situations. After a certain point, the
transgression of regulatory limits caused by `uncontrollable acts of
third parties,' such as strikes, sabotage, operator intoxication or
insanity and a variety of other eventualities, must be a matter for the
administrative exercise of case-by-case enforcement discretion, not for
specification in advance by regulation.''). In addition, emissions
during a malfunction event can be significantly higher than emissions
at any other time of source operation. For example, if an air pollution
control device with 99-percent removal goes off-line as a result of a
malfunction (as might happen if, for example, the bags in a baghouse
catch fire) and the emission unit is a steady-state type unit that
would take days to shut down, the source would go from 99-percent
control to zero control until the control device was repaired. The
source's emissions during the malfunction
[[Page 8424]]
would be 100 times higher than during normal operations and the
emissions over a 4-day malfunction period would exceed the annual
emissions of the source during normal operations. As this example
illustrates, accounting for malfunctions could lead to standards that
are not reflective of (and significantly less stringent than) levels
that are achieved by a well-performing non-malfunctioning source. It is
reasonable to interpret CAA section 112 to avoid such a result. The
EPA's approach to malfunctions is consistent with CAA section 112 and
is a reasonable interpretation of the statute.
In the event that a source fails to comply with the applicable CAA
section 112 standards as a result of a malfunction event, the EPA would
determine an appropriate response based on, among other things, the
good faith efforts of the source to minimize emissions during
malfunction periods, including preventative and corrective actions, as
well as root cause analyses to ascertain and rectify excess emissions.
The EPA would also consider whether the source's failure to comply with
the CAA section 112 standard was, in fact, sudden, infrequent, not
reasonably preventable and was not instead caused in part by poor
maintenance or careless operation.
If the EPA determines that an enforcement action against a source
for violation of an emission standard is warranted, the source can
raise any and all defenses in that enforcement action and the federal
district court will determine what, if any, relief is appropriate. The
same is true for citizen enforcement actions. Similarly, the presiding
officer in an administrative proceeding can consider any defense raised
and determine whether administrative penalties are appropriate.
In summary, the EPA interpretation of the CAA and, in particular,
CAA section 112 is reasonable and encourages practices that will avoid
malfunctions. Administrative and judicial procedures for addressing
exceedances of the standards fully recognize that violations may occur
despite good faith efforts to comply and can accommodate those
situations.
In several prior CAA section 112 rules, the EPA had included an
affirmative defense to civil penalties for violations caused by
malfunctions in an effort to create a system that incorporates some
flexibility, recognizing that there is a tension, inherent in many
types of air regulation, to ensure adequate compliance while
simultaneously recognizing that despite the most diligent of efforts,
emission standards may be violated under circumstances entirely beyond
the control of the source. Although the EPA recognized that its case-
by-case enforcement discretion provides sufficient flexibility in these
circumstances, it included the affirmative defense to provide a more
formalized approach and more regulatory clarity. See Weyerhaeuser Co.
v. Costle, 590 F.2d 1011, 1057-58 (D.C. Cir. 1978) (holding that an
informal case-by-case enforcement discretion approach is adequate); but
see Marathon Oil Co. v. EPA, 564 F.2d 1253, 1272-73 (9th Cir. 1977)
(requiring a more formalized approach to consideration of ``upsets
beyond the control of the permit holder''). Under the EPA's regulatory
affirmative defense provisions, if a source could demonstrate in a
judicial or administrative proceeding that it had met the requirements
of the affirmative defense in the regulation, civil penalties would not
be assessed. Recently, the United States Court of Appeals for the
District of Columbia Circuit vacated an affirmative defense in one of
the EPA's CAA section 112 regulations. NRDC v. EPA, 749 F.3d 1055 (D.C.
Cir., 2014) (vacating affirmative defense provisions in CAA section 112
rule establishing emission standards for Portland cement kilns). The
court found that the EPA lacked authority to establish an affirmative
defense for private civil suits and held that under the CAA, the
authority to determine civil penalty amounts in such cases lies
exclusively with the courts, not the EPA. Specifically, the court
found: ``As the language of the statute makes clear, the courts
determine, on a case-by-case basis, whether civil penalties are
`appropriate.''' See NRDC, 2014 U.S. App. LEXIS 7281 at *21 (``[U]nder
this statute, deciding whether penalties are `appropriate' in a given
private civil suit is a job for the courts, not EPA.'').\36\ In light
of NRDC, the EPA is not including a regulatory affirmative defense
provision in the proposed rule. As explained above, if a source is
unable to comply with emissions standards as a result of a malfunction,
the EPA may use its case-by-case enforcement discretion to provide
flexibility, as appropriate. Further, as the United States Court of
Appeals for the District of Columbia Circuit recognized, in an EPA or
citizen enforcement action, the court has the discretion to consider
any defense raised and determine whether penalties are appropriate. Cf.
NRDC, 2014 U.S. App. LEXIS 7281 at *24 (arguments that violation were
caused by unavoidable technology failure can be made to the courts in
future civil cases when the issue arises). The same is true for the
presiding officer in EPA administrative enforcement actions.\37\
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\36\ The court's reasoning in NRDC v. EPA focuses on civil
judicial actions. The Court noted that ``EPA's ability to determine
whether penalties should be assessed for Clean Air Act violations
extends only to administrative penalties, not to civil penalties
imposed by a court.'' Id.
\37\ Although the NRDC v. EPA case does not address the EPA's
authority to establish an affirmative defense to penalties that is
available in administrative enforcement actions, the EPA is not
including such an affirmative defense in the proposed rule. As
explained above, such an affirmative defense is not necessary.
Moreover, assessment of penalties for violations caused by
malfunctions in administrative proceedings and judicial proceedings
should be consistent. CF. CAA section 113(e) (requiring both the
Administrator and the court to take specified criteria into account
when assessing penalties).
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a. 40 CFR 63.743(e) General Duty
We are proposing to revise the entry in the General Provisions
table for 40 CFR 63.6(e)(1)(i) by changing the ``yes'' in column 2 to a
``no.'' Section 63.6(e)(1)(i) describes the general duty to minimize
emissions. Some of the language in that section is no longer necessary
or appropriate in light of the elimination of the SSM exemption. We are
proposing instead to add general duty regulatory text at 40 CFR
63.743(e) that reflects the general duty to minimize emissions while
eliminating the reference to periods covered by an SSM exemption. The
current language in 40 CFR 63.6(e)(1)(i) characterizes what the general
duty entails during periods of SSM. With the elimination of the SSM
exemption, there is no need to differentiate between normal operations,
startup and shutdown and malfunction events in describing the general
duty. Therefore the language the EPA is proposing for 40 CFR 63.743(e)
does not include that language from 40 CFR 63.6(e)(1).
We are also proposing to revise the General Provisions table entry
for 40 CFR 63.6(e)(1)(ii) by changing the ``yes'' in column 2 to a
``no.'' Section 63.6(e)(1)(ii) imposes requirements that are not
necessary with the elimination of the SSM exemption or are redundant
with the general duty requirement being added at 40 CFR 63.743(e).
b. SSM Plan
We are proposing to revise the General Provisions table entry for
40 CFR 63.6(e)(3) by changing the ``yes'' in column 2 to a ``no.''
Generally, these paragraphs require development of an SSM plan and
specify SSM recordkeeping and reporting requirements related to the SSM
plan. As noted, the EPA is proposing to remove the SSM exemptions.
Therefore, affected units will be subject to an
[[Page 8425]]
emission standard during such events. The applicability of a standard
during such events will ensure that sources have ample incentive to
plan for and achieve compliance and, thus, the SSM plan requirements
are no longer necessary.
c. Compliance With Standards
We are proposing to revise the General Provisions table entry for
40 CFR 63.6(f)(1) by changing the ``yes'' in column 2 to a ``no.'' The
current language of 40 CFR 63.6(f)(1) exempts sources from non-opacity
standards during periods of SSM. As discussed above, the court in
Sierra Club v. EPA vacated the exemptions contained in this provision
and held that the CAA requires that some CAA section 112 standards
apply continuously. Consistent with Sierra Club, the EPA is proposing
to revise some standards in this rule to apply at all times.
d. 40 CFR 63.749(j) Performance Testing
We are proposing to revise the General Provisions table entry for
40 CFR 63.7(e)(1) by changing the ``yes'' in column 2 to a ``no.''
Section 63.7(e)(1) describes performance testing requirements. The EPA
is instead proposing to add a performance testing requirement at 40 CFR
63.749(j). The performance testing requirements we are proposing to add
differ from the General Provisions performance testing provisions in
several respects. The regulatory text does not include the language in
40 CFR 63.7(e)(1) that restated the SSM exemption and language that
precluded startup and shutdown periods from being considered
``representative'' for purposes of performance testing. The proposed
performance testing provisions will specify that performance testing of
controls must be conducted during representative operating conditions
of the applicable source, and may not take place during startup,
shutdown or malfunction of the applicable controlled surface coating
operations, controlled chemical milling maskant application operations
or controlled chemical depainting operations. As in 40 CFR 63.7(e)(1),
performance tests conducted under this subpart should not be conducted
during malfunctions because conditions during malfunctions are often
not representative of normal operating conditions. The EPA is proposing
to add language that requires the owner or operator to record the
process information that is necessary to document operating conditions
during the test and include in such record an explanation to support
that such conditions represent normal operation. Section 63.7(e)
requires that the owner or operator make available to the Administrator
such records ``as may be necessary to determine the condition of the
performance test'' available to the Administrator upon request, but
does not specifically require the information to be recorded. The
regulatory text the EPA is proposing to add to this provision builds on
that requirement and makes explicit the requirement to record the
information.
e. Monitoring
We are proposing to revise the General Provisions table entry for
40 CFR 63.8(c)(1)(i) and (iii) by changing the ``yes'' in column 2 to a
``no.'' The cross-references to the general duty and SSM plan
requirements in those subparagraphs are not necessary in light of other
requirements of 40 CFR 63.8 that require good air pollution control
practices (40 CFR 63.8(c)(1)) and that set out the requirements of a
quality control program for monitoring equipment (40 CFR 63.8(d)).
f. 40 CFR 63.752(a) Recordkeeping
We are proposing to revise the General Provisions table entry for
40 CFR 63.10(b)(2)(i) by changing the ``yes'' in column 2 to a ``no.''
Section 63.10(b)(2)(i) describes the recordkeeping requirements during
startup and shutdown. These recording provisions are no longer
necessary because the EPA is proposing that recordkeeping and reporting
applicable to normal operations will apply to startup and shutdown. In
the absence of special provisions applicable to startup and shutdown,
such as a startup and shutdown plan, there is no reason to retain
additional recordkeeping for startup and shutdown periods.
We are proposing to revise the General Provisions table entry for
40 CFR 63.10(b)(2)(ii) by changing the ``yes'' in column 2 to a ``no.''
Section 63.10(b)(2)(ii) describes the recordkeeping requirements during
a malfunction. The EPA is proposing to add such requirements to 40 CFR
63.752(a). The regulatory text we are proposing to add differs from the
General Provisions it is replacing in that the General Provisions
requires the creation and retention of a record of the occurrence and
duration of each malfunction of process, air pollution control and
monitoring equipment. The EPA is proposing that this requirement apply
to any failure to meet an applicable standard and is requiring that the
source record the date, time and duration of the failure rather than
the ``occurrence.'' The EPA is also proposing to add to 40 CFR
63.752(a) a requirement that sources keep records that include a list
of the affected source or equipment and actions taken to minimize
emissions, an estimate of the quantity of each regulated pollutant
emitted over the standard for which the source failed to meet the
standard and a description of the method used to estimate the
emissions. Examples of such methods would include mass balance
calculations, measurements when available or engineering judgment based
on known process parameters (e.g., coating HAP content and application
rate or control device efficiencies). The EPA is proposing to require
that sources keep records of this information to ensure that there is
adequate information to allow the EPA to determine the severity of any
failure to meet a standard and to provide data that may document how
the source met the general duty to minimize emissions when the source
has failed to meet an applicable standard.
We are proposing to revise the General Provisions table entry for
40 CFR 63.10(b)(2)(iv) by changing the ``yes'' in column 2 to a ``no.''
When applicable, the provision requires sources to record actions taken
during SSM events when actions were inconsistent with their SSM plan.
The requirement is no longer appropriate because SSM plans will no
longer be required. The requirement previously applicable under 40 CFR
63.10(b)(2)(iv)(B) to record actions to minimize emissions and record
corrective actions is now applicable by reference to 40 CFR 63.752(a).
We are proposing to revise the General Provisions table entry for
40 CFR 63.10(b)(2)(v) by changing the ``yes'' in column 2 to a ``no.''
When applicable, the provision requires sources to record actions taken
during SSM events to show that actions taken were consistent with their
SSM plan. The requirement is no longer appropriate because SSM plans
will no longer be required.
g. 40 CFR 63.753 Reporting
We are proposing to revise the General Provisions table entry for
40 CFR 63.10(d)(5) by changing the ``yes'' in column 2 to a ``no.''
Section 63.10(d)(5) describes the reporting requirements for startups,
shutdowns and malfunctions. To replace the General Provisions reporting
requirement, the EPA is proposing to add reporting requirements to 40
CFR 63.753(a). The replacement language added to 40 CFR 63.753(a)
differs from the General Provisions requirement in that it eliminates
periodic SSM reports
[[Page 8426]]
as a stand-alone report. We are proposing language that requires
sources that fail to meet an applicable standard at any time to report
the information concerning such events in the semi-annual reporting
period already required under this rule. We are proposing that the
report must contain the number, date, time, duration and the cause of
such events (including unknown cause, if applicable), a list of the
affected source or equipment, an estimate of the quantity of each
regulated pollutant emitted over any emission limit and a description
of the method used to estimate the emissions.
Examples of such methods would include mass balance calculations,
measurements when available or engineering judgment based on known
process parameters (e.g., coating HAP content and application rates and
control device efficiencies). The EPA is proposing this requirement to
ensure that there is adequate information to determine compliance, to
allow the EPA to determine the severity of the failure to meet an
applicable standard and to provide data that may document how the
source met the general duty to minimize emissions during a failure to
meet an applicable standard.
We would no longer require owners or operators to determine whether
actions taken to correct a malfunction are consistent with an SSM plan,
because plans would no longer be required. The proposed amendments
would, therefore, eliminate the cross reference to 40 CFR
63.10(d)(5)(i) that contains the description of the previously required
SSM report format and submittal schedule from this section. These
specifications would be no longer necessary because the events would be
reported in otherwise required reports with similar format and
submittal requirements.
As discussed above, we are proposing to revise the General
Provisions table entry for 40 CFR 63.10(d)(5), by changing the ``yes''
in column 2 to a ``no.'' Section 63.10(d)(5)(ii) describes an immediate
report for startups, shutdown and malfunctions when a source failed to
meet an applicable standard, but did not follow the SSM plan. We will
no longer require owners and operators to report when actions taken
during a startup, shutdown or malfunction were not consistent with an
SSM plan, because plans would no longer be required to allow the EPA to
determine the severity of the failure to meet an applicable standard
and to provide data that may document how the source met the general
duty to minimize emissions during a failure to meet an applicable
standard.
4. Technical Amendments to the Aerospace NESHAP
The EPA is also proposing the following technical corrections:
Revising 40 CFR 63.743(a)(2) to match the section title in
40 CFR 63.5.
Revising 40 CFR 63.743(a)(8) to correct the reference to
paragraph 63.6(i)(12)(iii)(B) by changing the ``(1)'' to an ``(i).''
Revising 40 CFR 63.744(a) to correct and clarify the
format of the reference to 40 CFR 63.744(a)(1) through (4).
Correct the ordering of 40 CFR 63.744(a)(3) and (4);
currently paragraph (a)(4) is printed before (a)(3).
Correcting the paragraph numbering for 40 CFR
63.746(b)(4)(ii)(C) by changing paragraph (C) from a lower case to
upper case ``C.''
Correcting the numbering of the tables in 40 CFR 63.745 to
account for the proposed addition of Table 1 to that section to include
specialty coating limits.
Revising 40 CFR 63.749(d)(4) to correct the references to
40 CFR 63.749(d)(4)(i) through (d)(4)(iv) and (e).
Revising 40 CFR 63.750(g)(6)(i) to remove the letters
``VR/FD'' that were inadvertently included.
5. Amendments To Simplify Recordkeeping and Reporting for Compliant
Coatings
The EPA is proposing to revise 40 CFR 63.750 to include alternative
compliance demonstration provisions for all coatings subject to the
Aerospace NESHAP (primers, topcoats, specialty coatings and chemical
milling maskants). If the manufacturer's supplied formulation data or
calculation of HAP and VOC content indicate that the coating meets the
organic HAP and VOC content emission limits for its coating type, as
specified in 40 CFR 63.745(c) and 63.747(c), then the owner or operator
would not be required to demonstrate compliance for these coatings
using the test method and calculations specified in 40 CFR 63.750(c),
(e), (k) and (m) or to keep the associated records and submit the
associated reports associated with these methods and calculations.
Instead, the owner or operator would be able to rely on the
manufacturers' formulation data and calculation of the HAP or VOC
content to demonstrate compliance. However, the owner or operator would
still be required to maintain purchase records and manufacturer's
supplied data sheets for these compliant coatings. Owners or operators
of facilities using these coatings would also still be required to
handle and transfer these coatings in a manner that minimizes spills,
apply these coatings using one or more of the specified application
techniques and comply with inorganic HAP emission requirements.
This change is being proposed to reduce unnecessary recordkeeping
and avoid the need for owners or operators to perform tests to measure
VOC and HAP content and to perform certain calculations that can be
done by the coating manufacturer based on coating formulation data.
When the Aerospace NESHAP was originally promulgated, the original
compliance demonstration and recordkeeping requirements were needed
because the product data sheets provided by coating manufacturers did
not routinely provide VOC content in grams per liter (less water and
exempt solvents) or HAP content in grams per liter (less water). As a
result, it was necessary for the facilities to calculate the VOC or HAP
content in this format to demonstrate compliance.
Since promulgation of the Aerospace NESHAP, coating manufacturers
now commonly provide VOC content of the coatings, in grams per liter
(less water and exempt solvents) on the product data sheets, based on
coating formulation. Therefore, the coating manufacturer's
documentation can be used to demonstrate compliance, when available, in
place of the compliance demonstrations based on VOC measurements and
compliance calculations.
We are proposing that this alternative apply to all coatings
subject to the Aerospace NESHAP, including specialty coatings,
topcoats, primers and chemical milling maskants. Due to the existence
of the Aerospace NESHAP for nearly 20 years and the prevalence of state
and regional VOC regulations for many types of coatings, coating
manufacturers have come to recognize the value of providing
documentation of HAP and VOC content to their customers to facilitate
compliance demonstrations with state and federal regulations. For all
coatings subject to the Aerospace NESHAP, the EPA has determined that
onsite purchase records and the manufacturer's supplied data sheets for
the coatings will provide sufficient information to establish
compliance with the content limit standards in the Aerospace NESHAP.
If a facility elects to comply with the averaging provisions in 40
CFR 63.743(d), the facility is also required to comply with all related
averaging provisions in the Aerospace NESHAP for all coatings included
in averaging (e.g., compliance determination provisions in 40 CFR
63.749(d) and (h); procedures and methods in 40 CFR 63.750(d), (f), (l)
and (n); recordkeeping
[[Page 8427]]
provisions in 40 CFR 63.752(c) and (f); and reporting provisions in
63.753(c) and (e)). Note that, in complying with the current averaging
provisions, facilities may already use manufacturers' data for coatings
to determine the organic HAP and VOC weight fraction of coatings to
perform the calculations in 40 CFR 63.750(d), (f), (l) and (n).
F. What compliance dates are we proposing?
The EPA is proposing that all of the amendments being proposed in
this action would be effective on the date 60 days after these proposed
amendments are final, with one exception. The one exception is that
existing specialty coating affected sources (i.e., existing on the date
these changes are final) would have 1 year after the date this rule is
final to comply with the standards for specialty coatings proposed in
40 CFR 63.745(c)(5) and (6) (HAP and VOC limits for specified coatings)
and the provisions in 40 CFR 63.745(f) (coating application equipment)
and 40 CFR 63.745(g) (control of inorganic HAP emissions). The EPA is
proposing this compliance schedule so that existing sources would have
time to develop the recordkeeping and reporting systems needed to
comply with the requirements for specialty coatings. Facilities may
also need this time to identify alternative coatings for those that are
not currently compliant with the HAP or VOC content limits and to take
any steps needed to upgrade specialty coating operations to comply with
the application equipment requirements in 40 CFR 63.745(f) and the
inorganic HAP emissions requirements in 40 CFR 63.745(g).
The tasks necessary for existing facilities to comply with the
other proposed amendments require no time or resources. Therefore, EPA
believes that existing facilities will be able to comply with the other
proposed amendments, including those related to SSM periods, as soon as
the final rule is effective, which will be the date 60 days after
publication of the final rule. Therefore, the EPA is specifically
soliciting comment and additional data on the burden of complying with
the other proposed amendments.
V. Summary of Cost, Environmental and Economic Impacts
A. What are the affected sources?
The EPA estimates, based on the responses to the 2011 ICR, that
there are 144 major source facilities that are engaged in aerospace
manufacturing and rework surface coating operations. The EPA estimates
that 109 facilities likely would be affected by the proposed limits for
specialty coatings and the requirements to use high-efficiency
application equipment for specialty coatings, also based on the
responses to the 2011 ICR.
B. What are the air quality impacts?
The EPA estimates that annual HAP emissions from specialty coatings
are about 360 tpy; inorganic HAP emissions are about 5 tpy and the
remainder are organic HAP. The estimated emission reductions are 58
tons of HAP, which would be achieved from the proposed regulation of
specialty coatings. The EPA estimated that these emission reductions
would result from the proposed requirements to use high-efficiency
application equipment and also from the application of the HAP content
limits to specialty coatings.
C. What are the cost impacts?
The EPA estimates that the annual cost impacts would be about
$590,000 per year. The cost impacts would be attributed to monitoring
and recordkeeping costs for complying with the specialty coating HAP
content limits. The cost per facility was estimated based on the number
of specialty coatings used at each facility, as reported in the 2011
ICR. The costs are based on an assumption of 1 hour of technical labor
for annual recordkeeping and reporting for each specialty coating used
by a facility, plus additional management and clerical hours
representing a fraction of the technical labor hours.
The EPA does not have sufficient data from the 2011 ICR to estimate
the total cost impacts for specialty coatings having to comply with the
proposed high-efficiency application equipment requirement. Because
high-efficiency application equipment generates less coating overspray
than conventional equipment, the costs of upgrading to new equipment
can be offset by cost savings from reduced coating consumption and
reduced spray booth filter maintenance. For these reasons, many
facilities are likely to have already switched to high-efficiency
application methods for specialty coating operations, as they are
already required to for primer and topcoat application operations. For
example, the average volume of specialty coatings used per facility is
3,000 gallons per year, based on the 2011 ICR data. The estimated
purchase cost for a professional quality HVLP spray gun is $700 for the
gun and hoses. If the average facility had to purchase three new spray
guns, and the facility was spending an average of $30 per gallon of
spray applied coating, the facility would need to see a decrease in
coating consumption of only 70 gallons per year (about a 3-percent
reduction) to recover the initial cost of those three spray guns in 1
year.
The EPA expects some additional potential cost savings from the
proposal to include an alternative compliance demonstration provision
in 40 CFR 63.750(c), (e), (k) and (m). However, we do not have
sufficient data to estimate the cost savings associated with the
proposed alternative compliance demonstration. However, the estimated
cost to perform an analysis of VOC content according to EPA Method 24,
based on published vendor data, is about $575 per sample. Because the
proposed alternative compliance demonstration would allow facilities to
use coating manufacturers' documentation of VOC content based on
coating composition, the cost of these coating analyses using EPA
Method 24 would be avoided.
The EPA's cost analyses are documented in the memorandum,
Methodology for Estimating Control Costs for Specialty Coating
Operations in the Aerospace Source Category, January 2014, in the
docket for this rulemaking.
EPA is specifically soliciting comment and additional data on the
cost impacts associated with using coatings that are compliant with the
proposed limits for specialty coatings.
D. What are the economic impacts?
Economic impact analyses focus on changes in market prices and
output levels. If changes in market prices and output levels in the
primary markets are significant enough, impacts on other markets are
also examined. Both the magnitude of costs needed to comply with the
rule and the distribution of these costs among affected facilities can
have a role in determining how the market will change in response to a
rule.
This rule applies to the surface coating and related operations at
facilities that are major sources and are engaged, either in part or in
whole, in the manufacture or rework of commercial, civil or military
aerospace vehicles or components. The proposed rule would add
recordkeeping and reporting provisions for specialty coating
operations, but would not change the compliance costs for operations
already being regulated by the existing emission standards. Therefore,
the annual costs were calculated for only the 109 Aerospace
Manufacturing and Rework Facilities that reported having specialty
coating operations.
[[Page 8428]]
The estimated annual costs for this proposed rule are less than $1
million in the first year and in succeeding years (less than $850,000
in the first year and less than $600,000 in succeeding years). These
costs are estimated for the 109 facilities that, based on information
reported by facilities, appear to have specialty coating operations.
Thus, the average cost per facility is less than $10,000 per year.
These costs are small compared to sales for the companies in aerospace
manufacturing and reworking. For example, in 2012 the average annual
value of shipments (a rough estimate of sales) for firms in the
category of ``other aircraft parts and auxiliary equipment
manufacturing'' was almost $50 million (Source: U.S. Census Bureau,
2012 Economic Census for NAICS 336413 for 2012). In this case the cost-
to-sales estimate would be approximately 0.02 percent of sales for each
firm. Costs this small would not have significant market impacts,
whether they were absorbed by the firm or passed on as price increases.
The EPA does not know of any firms that are small entities and
using specialty coatings that are potentially subject to this proposed
rule. Because no small firms face control costs, there is no
significant impact on small entities. Therefore, we do not expect these
proposed amendments to have a significant impact on a substantial
number of small entities.
E. What are the benefits?
We anticipate this rulemaking to reduce organic and inorganic HAP
emissions by approximately 58 tons each year. These avoided emissions
will result in improvements in air quality and reduced negative health
effects associated with exposure to air pollution of these emissions.
However, we have not quantified or monetized the benefits of reducing
these emissions for this rulemaking because the estimated costs for
this action are less than $100 million.
VI. Request for Comments
We solicit comments on all aspects of this proposed action. In
addition to general comments on this proposed action, we are also
interested in additional data that may improve the risk assessments and
other analyses. We are specifically interested in receiving any
improvements to the data used in the site-specific emissions profiles
used for risk modeling. Such data should include supporting
documentation in sufficient detail to allow characterization of the
quality and representativeness of the data or information. Section VII
of this preamble provides more information on submitting data.
VII. Submitting Data Corrections
The site-specific emissions profiles used in the source category
risk and demographic analyses and instructions are available for
download on the RTR Web site at: https://www.epa.gov/ttn/atw/rrisk/rtrpg.html. The data files include detailed information for each HAP
emissions release point for the facilities in the source category.
If you believe that the data are not representative or are
inaccurate, please identify the data in question, provide your reason
for concern and provide any ``improved'' data that you have, if
available. When you submit data, we request that you provide
documentation of the basis for the revised values to support your
suggested changes. To submit comments on the data downloaded from the
RTR page, complete the following steps:
1. Within this downloaded file, enter suggested revisions to the
data fields appropriate for that information.
2. Fill in the commenter information fields for each suggested
revision (i.e., commenter name, commenter organization, commenter email
address, commenter phone number and revision comments).
3. Gather documentation for any suggested emissions revisions
(e.g., performance test reports, material balance calculations, etc.).
4. Send the entire downloaded file with suggested revisions in
Microsoft[supreg] Access format and all accompanying documentation to
Docket ID No. EPA-HQ-OAR-2014-0830 (through one of the methods
described in the ADDRESSES section of this preamble).
5. If you are providing comments on a single facility or multiple
facilities, you need only submit one file for all facilities. The file
should contain all suggested changes for all sources at that facility.
We request that all data revision comments be submitted in the form of
updated Microsoft[supreg] Excel files that are generated by the
Microsoft[supreg] Access file. These files are provided on the RTR Web
site at: https://www.epa.gov/ttn/atw/rrisk/rtrpg.html.
VIII. Statutory and Executive Order Reviews
Additional information about these statutes and Executive Orders
can be found at https://www2.epa.gov/laws-regulations/laws-and-executive-orders.
A. Executive Order 12866: Regulatory Planning and Review and Executive
Order 13563: Improving Regulation and Regulatory Review
This action is not a significant regulatory action and was
therefore not submitted to the OMB for review.
B. Paperwork Reduction Act (PRA)
The information collection activities in this proposed rule have
been submitted for approval to the OMB under the PRA. The ICR document
that the EPA prepared has been assigned EPA ICR number 1687.10. You can
find a copy of the ICR in the docket for this rule, and it is briefly
summarized here.
Respondents are owners or operators of aerospace manufacturing and
rework operations. The proposed rule would add recordkeeping and
reporting provisions for specialty coating operations, but would not
change the recordkeeping and reporting provisions for any other types
of operations. Therefore, of the 144 Aerospace Manufacturing and Rework
Facilities subject to the Aerospace NESHAP, the annual costs for
increased recordkeeping and reporting would apply to only the 109
Aerospace Manufacturing and Rework Facilities that reported having
specialty coating operations. Respondents must keep records of the
specialty coatings used at the facility, including the name and VOC
content of the coating, the HAP and VOC emitted per gallon of coating
and the monthly volume of each coating used. Respondents must also
submit semiannual reports of noncompliance. Recordkeeping and reporting
of monitored parameters related to air pollution control technologies
is required if controls are used to demonstrate compliance with the
standards. The reports and records will be used to determine compliance
with the standards.
Respondents/affected entities: Aerospace manufacturing and rework
facilities using specialty coatings.
Respondent's obligation to respond: Mandatory (40 CFR part 63,
subpart GG).
Estimated number of respondents: 109 facilities using specialty
coatings.
Frequency of response: Initially, occasionally and semiannually.
Total estimated burden: 6,914 hours (per year) for the responding
facilities and 148 hours (per year) for the agency. These are estimates
for the average annual burden for the first 3 years after the rule is
final. Burden is defined at 5 CFR 1320.3(b).
Total estimated cost: $695,570 (per year), which includes no
annualized
[[Page 8429]]
capital or operation and maintenance costs, for the responding
facilities and $8,740 (per year) for the agency. These are estimates
for the average annual cost for the first 3 years after the rule is
final.
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 the
EPA's regulations in 40 CFR are listed in 40 CFR part 9. 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, the EPA has established a public docket for this rule, which
includes this ICR, under Docket ID No. EPA-HQ-OAR-2014-0830.
Submit your comments on the Agency's need for this information, the
accuracy of the provided burden estimates and any suggested methods for
minimizing respondent burden to the EPA using the docket identified at
the beginning of this rule. You may also send your ICR-related comments
to OMB's Office of Information and Regulatory Affairs via email to
oria_submissions@omb.eop.gov, Attention: Desk Officer for the EPA.
Since OMB is required to make a decision concerning the ICR between 30
and 60 days after receipt, OMB must receive comments no later than
March 19, 2015. The EPA will respond to any ICR-related comments in the
final rule.
C. Regulatory Flexibility Act (RFA)
I certify that this action will not have a significant economic
impact on a substantial number of small entities under the RFA. This
action will not impose any requirements on small entities. No
facilities meeting the Small Business Administration's definition of a
small business would face significant control costs, based on the
economic impact analysis completed for this action. The results of this
analysis are summarized in section V.D of this preamble and can be
found in the memorandum, Economic Impact Analysis for Proposed National
Emission Standards for Aerospace Manufacturing and Rework Facilities,
December 3, 2014. A copy of this memorandum is in the docket for this
rulemaking.
D. Unfunded Mandates Reform Act (UMRA)
This action does not contain an unfunded mandate of $100 million or
more as described in the UMRA, 2 U.S.C. 1531-1538, and does not
significantly or uniquely affect small governments. The action imposes
no enforceable duty on any state, local or tribal governments or the
private sector.
E. Executive Order 13132: Federalism
This action 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.
F. Executive Order 13175: Consultation and Coordination With Indian
Tribal Governments
This action does not have tribal implications as specified in
Executive Order 13175. No tribal facilities are known to be engaged in
the aerospace manufacturing or rework surface coating operations that
would be affected by this action. Thus, Executive Order 13175 does not
apply to this action.
G. Executive Order 13045: Protection of Children From Environmental
Health Risks and Safety Risks
This action is not subject to Executive Order 13045 because it is
not economically significant as defined in Executive Order 12866, and
because the EPA does not believe the environmental health or safety
risks addressed by this action present a disproportionate risk to
children. This action's health and risk assessments are contained in
sections III.A and B and sections IV.B and C of this preamble.
H. Executive Order 13211: Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution or Use
This action is not subject to Executive Order 13211 because it is
not a significant regulatory action under Executive Order 12866.
I. National Technology Transfer and Advancement Act (NTTAA)
This rulemaking does not involve technical standards.
J. Executive Order 12898: Federal Actions to Address Environmental
Justice in Minority Populations and Low-Income Populations
The EPA believes the human health or environmental risk addressed
by this action will not have potential disproportionately high and
adverse human health or environmental effects on minority, low-income
or indigenous populations.
These proposed standards will improve public health and welfare,
now and in the future, by reducing HAP emissions contributing to
environmental and human health impacts. These reductions in HAP
associated with the rule are expected to benefit all populations.
To examine the potential for any environmental justice issues that
might be associated with the Aerospace Manufacturing and Rework source
category, we evaluated the distributions of HAP related cancer and non-
cancer risks across different social, demographic and economic groups
within the populations living near the facilities where this source
category is located. The methods used to conduct demographic analyses
for this proposed rule are described in the document, Risk and
Technology Review--Analysis of Socio-Economic Factors for Populations
Living Near Aerospace Facilities, which may be found in the docket for
this rulemaking (Docket ID No. EPA-HQ-OAR-2014-0830).
In the demographics analysis, we focused on populations within 50
km of the facilities in this source category with emissions sources
subject to the MACT standard. More specifically, for these populations,
we evaluated exposures to HAP that could result in cancer risks of 1-
in-1 million or greater. We compared the percentages of particular
demographic groups within the focused populations to the total
percentages of those demographic groups nationwide. The results of this
analysis are documented in the document, Risk and Technology Review--
Analysis of Socio-Economic Factors for Populations Living Near
Aerospace Facilities.
List of Subjects in 40 CFR Part 63
Environmental protection, Air pollution control, Hazardous
substances, Reporting and recordkeeping requirements.
Dated: January 22, 2015.
Gina McCarthy,
Administrator.
For the reasons stated in the preamble, part 63 of title 40,
chapter I, of the Code of Federal Regulations is proposed to be amended
as follows:
PART 63--NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS
FOR SOURCE CATEGORIES
0
1. The authority citation for part 63 continues to read as follows:
Authority: 42 U.S.C. 7401, et seq.
Subpart GG--National Emission Standards for Aerospace Manufacturing
and Rework Facilities
0
2. Section 63.741 is amended by:
[[Page 8430]]
0
a. Revising paragraph (c) introductory text;
0
b. Redesignating paragraphs (c)(4) through (c)(7) as paragraphs (c)(5)
through (c)(8);
0
c. Adding new paragraph (c)(4);
0
d. Revising newly redesignated paragraph (c)(8); and
0
e. Revising paragraphs (f) and (g).
The revisions and addition read as follows:
Sec. 63.741 Applicability and designation of affected sources.
* * * * *
(c) Affected sources. The affected sources to which the provisions
of this subpart apply are specified in paragraphs (c)(1) through (8) of
this section. The activities subject to this subpart are limited to the
manufacture or rework of aerospace vehicles or components as defined in
this subpart. Where a dispute arises relating to the applicability of
this subpart to a specific activity, the owner or operator shall
demonstrate whether or not the activity is regulated under this
subpart.
* * * * *
(4) For organic HAP or VOC emissions, each specialty coating
application operation, which is the total of all specialty coating
applications at the facility.
* * * * *
(8) For inorganic HAP emissions, each spray booth or hangar that
contains a primer, topcoat or specialty coating application operation
subject to Sec. 63.745(g), or a depainting operation subject to Sec.
63.746(b)(4).
* * * * *
(f) This subpart does not regulate research and development,
quality control and laboratory testing activities, chemical milling,
metal finishing, electrodeposition (except for electrodeposition of
paints), composites processing (except for cleaning and coating of
composite parts or components that become part of an aerospace vehicle
or component as well as composite tooling that comes in contact with
such composite parts or components prior to cure), electronic parts and
assemblies (except for cleaning and topcoating of completed
assemblies), manufacture of aircraft transparencies and wastewater
operations at aerospace facilities. These requirements do not apply to
the rework of aircraft or aircraft components if the holder of the
Federal Aviation Administration (FAA) design approval, or the holder's
licensee, is not actively manufacturing the aircraft or aircraft
components. These requirements also do not apply to parts and
assemblies not critical to the vehicle's structural integrity or flight
performance. The requirements of this subpart also do not apply to
primers, topcoats, specialty coatings, chemical milling maskants,
strippers and cleaning solvents containing HAP and VOC at
concentrations less than 0.1 percent by mass for carcinogens or 1.0
percent by mass for noncarcinogens, as determined from manufacturer's
representations, such as in a material safety data sheet or product
data sheet or testing. Additional specific exemptions from regulatory
coverage are set forth in paragraphs (e), (g), (h), (i) and (j) of this
section and Sec. Sec. 63.742, 63.744(a)(1), (b), (e), 63.745(a),
(f)(3), (g)(4), 63.746(a), (b)(5), 63.747(c)(3) and 63.749(d).
(g) The requirements for primers, topcoats, specialty coatings and
chemical milling maskants in Sec. Sec. 63.745 and 63.747 do not apply
to the use of low-volume coatings in these categories for which the
annual total of each separate formulation used at a facility does not
exceed 189 liters (50 gal), and the combined annual total of all such
primers, topcoats, specialty coatings and chemical milling maskants
used at a facility does not exceed 757 liters (200 gal). Primers,
topcoats and specialty coatings exempted under paragraph (f) of this
section and under Sec. 63.745(f)(3) and (g)(4) are not included in the
50 and 200 gal limits. Chemical milling maskants exempted under Sec.
63.747(c)(3) are also not included in these limits.
* * * * *
0
3. Section 63.742 is amended by revising the definitions for ``Chemical
milling maskant''; ``Softener''; and ``Stripper'' to read as follows:
Sec. 63.742 Definitions.
* * * * *
Chemical milling maskant means a coating that is applied directly
to aluminum components to protect surface areas when chemical milling
the component with a Type I or Type II etchant. Type I chemical milling
maskants are used with a Type I etchant and Type II chemical milling
maskants are used with a Type II etchant. This definition does not
include bonding maskants, critical use and line sealer maskants and
seal coat maskants. Additionally, maskants that must be used with a
combination of Type I or II etchants and any of the above types of
maskants (i.e., bonding, critical use and line sealer and seal coat)
are also not included in this definition. (See also Type I and Type II
etchant definitions.)
* * * * *
Softener means a liquid that is applied to an aerospace vehicle or
component to degrade coatings such as primers, topcoats and specialty
coatings specifically as a preparatory step to subsequent depainting by
non-chemical based depainting equipment. Softeners may contain VOC, but
shall not contain any HAP as determined from MSDS's or manufacturer
supplied information.
* * * * *
Stripper means a liquid that is applied to an aerospace vehicle or
component to remove permanent coatings such as primers, topcoats and
specialty coatings.
* * * * *
0
4. Section 63.743 is amended by:
0
a. Revising paragraphs (a)(2), (8), and (10);
0
b. Removing and reserving paragraph (b);
0
c. Revising paragraphs (d)(1), (2), and (3);
0
d. Removing and reserving paragraphs (d)(4) and (5);
0
e. Adding paragraph (e).
The revisions and addition read as follows:
Sec. 63.743 Standards: General.
(a) * * *
(2) Sec. 63.5, Preconstruction review and notification
requirements; and
* * * * *
(8) For the purposes of this subpart, each owner or operator is to
be provided 30 calendar days to present additional information to the
Administrator after he/she is notified of the intended denial of a
compliance extension request submitted under either Sec. 63.6(i)(4) or
(5), rather than 15 calendar days as provided for in Sec.
63.6(i)(12)(iii)(B) and Sec. 63.6(i)(13)(iii)(B).
* * * * *
(10) For the purposes of compliance with the requirements of Sec.
63.5(b)(4) of the General Provisions and this subpart, owners or
operators of existing primer, topcoat or specialty coating application
operations and depainting operations who construct or reconstruct a
spray booth or hangar that does not have the potential to emit 10 tons/
yr or more of an individual inorganic HAP or 25 tons/yr or more of all
inorganic HAP combined shall only be required to notify the
Administrator of such construction or reconstruction on an annual
basis. Notification shall be submitted on or before March 1 of each
year and shall include the information required in Sec. 63.5(b)(4) for
each such spray booth or hangar constructed or reconstructed during the
prior calendar year, except that such information shall be limited to
inorganic HAP's. No advance notification or written approval from the
Administrator pursuant to Sec. 63.5(b)(3) shall be required for the
[[Page 8431]]
construction or reconstruction of such a spray booth or hangar unless
the booth or hangar has the potential to emit 10 tons/yr or more of an
individual inorganic HAP or 25 tons/yr or more of all inorganic HAP
combined.
* * * * *
(d) * * *
(1) Each owner or operator of a new or existing source shall use
any combination of primers, topcoats (including self-priming topcoats),
specialty coatings, Type I chemical milling maskants or Type II
chemical milling maskants such that the monthly volume-weighted average
organic HAP and VOC contents of the combination of primers, topcoats,
specialty coatings, Type I chemical milling maskants or Type II
chemical milling maskants, as determined in accordance with the
applicable procedures set forth in Sec. 63.750, complies with the
specified content limits in Sec. Sec. 63.745(c) and 63.747(c), unless
the permitting agency specifies a shorter averaging period as part of
an ambient ozone control program.
(2) Averaging is allowed only for uncontrolled primers, topcoats
(including self-priming topcoats), specialty coatings, Type I chemical
milling maskants or Type II chemical milling maskants.
(3) Averaging is not allowed between specialty coating types
defined in Appendix A to this subpart, or between the different types
of coatings specified in paragraphs (d)(3)(i) through (vii) of this
section.
(i) Primers and topcoats (including self-priming topcoats).
(ii) Type I and Type II chemical milling maskants.
(iii) Primers and chemical milling maskants.
(iv) Topcoats and chemical milling maskants.
(v) Primers and specialty coatings.
(vi) Topcoats and specialty coatings.
(vii) Chemical milling maskants and specialty coatings.
* * * * *
(e) At all times, the owner or operator must operate and maintain
any affected source, including associated air pollution control
equipment and monitoring equipment, in a manner consistent with safety
and good air pollution control practices for minimizing emissions. The
general duty to minimize emissions does not require the owner or
operator to make any further efforts to reduce emissions if levels
required by the applicable standard have been achieved. Determination
of whether a source is operating in compliance with operation and
maintenance requirements will be based on information available to the
Administrator which may include, but is not limited to, monitoring
results, review of operation and maintenance procedures, review of
operation and maintenance records and inspection of the source.
0
5. Section 63.744 is amended by:
0
a. Revising paragraph (a) introductory text; and
0
b. Correcting the numerical order of paragraphs (a)(3) and (4).
The revision reads as follows:
Sec. 63.744 Standards: Cleaning operations.
(a) Housekeeping measures. Each owner or operator of a new or
existing cleaning operation subject to this subpart shall comply with
the requirements in paragraphs (a)(1) through (4) of this section
unless the cleaning solvent used is identified in Table 1 of this
section or contains HAP and VOC below the de minimis levels specified
in Sec. 63.741(f).
* * * * *
0
6. Section 63.745 is amended by:
0
a. Revising the section heading;
0
b. Revising paragraphs (a), (b), and (c) introductory text;
0
c. Adding paragraphs (c)(5), (c)(6) and Table 1;
0
d. Revising paragraphs (e) introductory text and (e)(1);
0
e. Revising paragraphs (f) introductory text, (f)(1) introductory text
and (f)(2);
0
f. Revising paragraphs (g) introductory text, (g)(2)(i), (g)(2)(ii),
and (g)(2)(iii)(B).
The revisions and additions read as follows:
Sec. 63.745 Standards: Primer, topcoat and specialty coating
application operations.
(a) Each owner or operator of a new or existing primer, topcoat or
specialty coating application operation subject to this subpart shall
comply with the requirements specified in paragraph (c) of this section
for those coatings that are uncontrolled (no control device is used to
reduce organic HAP emissions from the operation), and in paragraph (d)
of this section for those coatings that are controlled (organic HAP
emissions from the operation are reduced by the use of a control
device). Aerospace equipment that is no longer operational, intended
for public display and not easily capable of being moved is exempt from
the requirements of this section.
(b) Each owner or operator shall conduct the handling and transfer
of primers, topcoats and specialty coatings to or from containers,
tanks, vats, vessels and piping systems in such a manner that minimizes
spills.
(c) Uncontrolled coatings--organic HAP and VOC content levels. Each
owner or operator shall comply with the organic HAP and VOC content
limits specified in paragraphs (c)(1) through (6) of this section for
those coatings that are uncontrolled.
* * * * *
(5) Organic HAP emissions from specialty coatings shall be limited
to an organic HAP content level of no more than the HAP content limit
specified in Table 1 of this section for each applicable specialty
coating type.
(6) VOC emissions from specialty coatings shall be limited to a VOC
content level of no more than the VOC content limit specified in Table
1 of this section for each applicable specialty coating type.
Table 1--Specialty Coatings--HAP and VOC Content Limits
------------------------------------------------------------------------
HAP limit g/L VOC Limit g/L
Coating type (lb/gallon) (lb/gallon)
\1\ \1\
------------------------------------------------------------------------
Ablative Coating........................ 600 (5.0) 600 (5.0)
Adhesion Promoter....................... 890 (7.4) 890 (7.4)
Adhesive Bonding Primers: Cured at 250 850 (7.1) 850 (7.1)
[deg]F or below........................
Adhesive Bonding Primers: Cured above 1,030 (8.6) 1,030 (8.6)
250 [deg]F.............................
Commercial Interior Adhesive............ 760 (6.3) 760 (6.3)
Cyanoacrylate Adhesive.................. 1,020 (8.5) 1,020 (8.5)
Fuel Tank Adhesive...................... 620 (5.2) 620 (5.2)
Nonstructural Adhesive.................. 360 (3.0) 360 (3.0)
Rocket Motor Bonding Adhesive........... 890 (7.4) 890 (7.4)
Rubber-based Adhesive................... 850 (7.1) 850 (7.1)
Structural Autoclavable Adhesive........ 60 (0.5) 60 (0.5)
Structural Nonautoclavable Adhesive..... 850 (7.1) 850 (7.1)
[[Page 8432]]
Antichafe Coating....................... 660 (5.5) 660 (5.5)
Bearing Coating......................... 620 (5.2) 620 (5.2)
Caulking and Smoothing Compounds........ 850 (7.1) 850 (7.1)
Chemical Agent-Resistant Coating........ 550 (4.6) 550 (4.6)
Clear Coating........................... 720 (6.0) 720 (6.0)
Commercial Exterior Aerodynamic 650 (5.4) 650 (5.4)
Structure Primer.......................
Compatible Substrate Primer............. 780 (6.5) 780 (6.5)
Corrosion Prevention Compound........... 710 (5.9) 710 (5.9)
Cryogenic Flexible Primer............... 645 (5.4) 645 (5.4)
Cryoprotective Coating.................. 600 (5.0) 600 (5.0)
Dry Lubricative Material................ 880 (7.3) 880 (7.3)
Electric or Radiation-Effect Coating.... 800 (6.7) 800 (6.7)
Electrostatic Discharge and 800 (6.7) 800 (6.7)
Electromagnetic Interference (EMI)
Coating................................
Elevated-Temperature Skydrol-Resistant 740 (6.2) 740 (6.2)
Commercial Primer......................
Epoxy Polyamide Topcoat................. 660 (5.5) 660 (5.5)
Fire-Resistant (interior) Coating....... 800 (6.7) 800 (6.7)
Flexible Primer......................... 640 (5.3) 640 (5.3)
Flight-Test Coatings: Missile or Single 420 (3.5) 420 (3.5)
Use Aircraft...........................
Flight-Test Coatings: All Other......... 840 (7.0) 840 (7.0)
Fuel-Tank Coating....................... 720 (6.0) 720 (6.0)
High-Temperature Coating................ 850 (7.1) 850 (7.1)
Insulation Covering..................... 740 (6.2) 740 (6.2)
Intermediate Release Coating............ 750 (6.3) 750 (6.3)
Lacquer................................. 830 (6.9) 830 (6.9)
Bonding Maskant......................... 1,230 (10.3) 1,230 (10.3)
Critical Use and Line Sealer Maskant.... 1,020 (8.5) 1,020 (8.5)
Seal Coat Maskant....................... 1,230 (10.3) 1,230 (10.3)
Metalized Epoxy Coating................. 740 (6.2) 740 (6.2)
Mold Release............................ 780 (6.5) 780 (6.5)
Optical Anti-Reflective Coating......... 750 (6.3) 750 (6.3)
Part Marking Coating.................... 850 (7.1) 850 (7.1)
Pretreatment Coating.................... 780 (6.5) 780 (6.5)
Rain Erosion-Resistant Coating.......... 850 (7.1) 850 (7.1)
Rocket Motor Nozzle Coating............. 660 (5.5) 660 (5.5)
Scale Inhibitor......................... 880 (7.3) 880 (7.3)
Screen Print Ink........................ 840 (7.0) 840 (7.0)
Extrudable/Rollable/Brushable Sealant... 280 (2.3) 280 (2.3)
Sprayable Sealant....................... 600 (5.0) 600 (5.0)
Silicone Insulation Material............ 850 (7.1) 850 (7.1)
Solid Film Lubricant.................... 880 (7.3) 880 (7.3)
Specialized Function Coating............ 890 (7.4) 890 (7.4)
Temporary Protective Coating............ 320 (2.7) 320 (2.7)
Thermal Control Coating................. 800 (6.7) 800 (6.7)
Wet Fastener Installation Coating....... 675 (5.6) 675 (5.6)
Wing Coating............................ 850 (7.1) 850 (7.1)
------------------------------------------------------------------------
\1\ Coating limits for HAP are expressed in terms of mass (grams or
pounds) of HAP per volume (liters or gallons) of coating less water.
Coating limits for VOC are expressed in terms of mass (grams or
pounds) of VOC per volume (liters or gallons) of coating less water
and less exempt solvent.
* * * * *
(e) Compliance methods. Compliance with the organic HAP and VOC
content limits specified in paragraphs (c)(1) through (6) of this
section shall be accomplished by using the methods specified in
paragraphs (e)(1) and (2) of this section either by themselves or in
conjunction with one another.
(1) Use primers, topcoats (including self-priming topcoats) and
specialty coatings with HAP and VOC content levels equal to or less
than the limits specified in paragraphs (c)(1) through (6) of this
section; or
* * * * *
(f) Application equipment. Except as provided in paragraph (f)(3)
of this section, each owner or operator of a new or existing primer,
topcoat (including self-priming topcoat) or specialty coating
application operation subject to this subpart in which any of the
coatings contain organic HAP or VOC shall comply with the requirements
specified in paragraphs (f)(1) and (2) of this section.
(1) All primers, topcoats (including self-priming topcoats) and
specialty coatings shall be applied using one or more of the
application techniques specified in paragraphs (f)(1)(i) through (ix)
of this section.
* * * * *
(2) All application devices used to apply primers, topcoats
(including self-priming topcoats) or specialty coatings shall be
operated according to company procedures, local specified operating
procedures and/or the manufacturer's specifications, whichever is most
stringent, at all times. Equipment modified by the facility shall
maintain a transfer efficiency equivalent to HVLP and electrostatic
spray application techniques.
* * * * *
(g) Inorganic HAP emissions. Except as provided in paragraph (g)(4)
of this section, each owner or operator of a new or existing primer,
topcoat or specialty coating application operation subject to this
subpart in which any of the coatings that are spray applied contain
[[Page 8433]]
inorganic HAP, shall comply with the applicable requirements in
paragraphs (g)(1) through (3) of this section.
* * * * *
(2) * * *
(i) For existing sources, the owner or operator must choose one of
the following:
(A) Before exhausting it to the atmosphere, pass the air stream
through a dry particulate filter system certified using the methods
described in Sec. 63.750(o) to meet or exceed the efficiency data
points in Tables 2 and 3 of this section; or
(C) Before exhausting it to the atmosphere, pass the air stream
through an air pollution control system that meets or exceeds the
efficiency data points in Tables 2 and 3 of this section and is
approved by the permitting authority.
Table 2--Two-Stage Arrestor; Liquid Phase Challenge for Existing Sources
------------------------------------------------------------------------
Aerodynamic
Filtration efficiency requirement, % particle size
range, [mu]m
------------------------------------------------------------------------
>90..................................................... >5.7
>50..................................................... >4.1
>10..................................................... >2.2
------------------------------------------------------------------------
Table 3--Two-Stage Arrestor; Solid Phase Challenge for Existing Sources
------------------------------------------------------------------------
Aerodynamic
Filtration efficiency requirement, % particle size
range, [mu]m
------------------------------------------------------------------------
>90..................................................... >8.1
>50..................................................... >5.0
>10..................................................... >2.6
------------------------------------------------------------------------
(ii) For new sources, either:
(A) Before exhausting it to the atmosphere, pass the air stream
through a dry particulate filter system certified using the methods
described in Sec. 63.750(o) to meet or exceed the efficiency data
points in Tables 4 and 5 of this section; or (B) Before exhausting it
to the atmosphere, pass the air stream through an air pollution control
system that meets or exceeds the efficiency data points in Tables 4 and
5 of this section and is approved by the permitting authority.
Table 4--Three-Stage Arrestor; Liquid Phase Challenge for New Sources
------------------------------------------------------------------------
Aerodynamic
Filtration efficiency requirement, % particle size
range, [mu]m
------------------------------------------------------------------------
>95..................................................... >2.0
>80..................................................... >1.0
>65..................................................... >0.42
------------------------------------------------------------------------
Table 5--Three-Stage Arrestor; Solid Phase Challenge for New Sources
------------------------------------------------------------------------
Aerodynamic
Filtration efficiency requirement, % particle size
range, [mu]m
------------------------------------------------------------------------
>95..................................................... >2.5
>85..................................................... >1.1
>75..................................................... >0.70
------------------------------------------------------------------------
(iii) * * *
(B) If the primer, topcoat or specialty coating contains chromium
or cadmium, control shall consist of a HEPA filter system, three-stage
filter system or other control system equivalent to the three stage
filter system as approved by the permitting agency.
* * * * *
0
7. Section 63.746 is amended by revising (b)(4)(ii)(A) and (B) to read
as follows:
Sec. 63.746 Standards: Depainting operations.
* * * * *
(b) * * *
(4) * * *
(ii)(A) For existing sources, pass any air stream removed from the
enclosed area or closed-cycle depainting system through a dry
particulate filter system, certified using the method described in
Sec. 63.750(o) to meet or exceed the efficiency data points in Tables
2 and 3 of Sec. 63.745, through a baghouse or through a waterwash
system before exhausting it to the atmosphere.
(B) For new sources, pass any air stream removed from the enclosed
area or closed-cycle depainting system through a dry particulate filter
system certified using the method described in Sec. 63.750(o) to meet
or exceed the efficiency data points in Tables 4 and 5 of Sec. 63.745
or through a baghouse before exhausting it to the atmosphere.
* * * * *
0
8. Section 63.749 is amended by:
0
a. Revising paragraphs (a)(1) and (2);
0
b. Adding paragraph (a)(3);
0
c. Revising paragraph (b);
0
d. Revising the heading of paragraph (d), paragraph (d)(4) introductory
text and paragraph (d)(4)(i);
0
e. Revising paragraph (e) introductory text;
0
f. Adding paragraph (j).
The revisions and additions read as follows:
Sec. 63.749 Compliance dates and determinations.
(a) * * * (1) Each owner or operator of an existing affected source
subject to this subpart shall comply with the requirements of this
subpart by September 1, 1998, except as specified in paragraphs (a)(2)
and (3) of this section. Owners or operators of new affected sources
subject to this subpart shall comply on the effective date or upon
startup, whichever is later. In addition, each owner or operator shall
comply with the compliance dates specified in Sec. 63.6(b) and (c) as
indicated in Table 1 to subpart GG of part 63.
(2) Owners or operators of existing primer, topcoat or specialty
coating application operations and depainting operations who construct
or reconstruct a spray booth or hangar must comply with the new source
requirements for inorganic HAP specified in Sec. Sec. 63.745(g)(2)(ii)
and 63.746(b)(4) for that new spray booth or hangar upon startup. Such
sources must still comply with all other existing source requirements
by September 1, 1998.
(3) Each owner or operator of a specialty coating application
operation that begins construction or reconstruction after [date of
publication of final rule in the Federal Register] shall be in
compliance with the requirements of this subpart on [date of
publication of final rule in the Federal Register] or upon startup,
whichever is later. Each owner or operator of a specialty coating
application operation that is existing on [date of publication of final
rule in the Federal Register] shall be in compliance with the
requirements of this subpart on or before [date 1 year after date of
publication of final rule in the Federal Register].
(b) General. Each facility subject to this subpart shall be
considered in noncompliance if the owner or operator fails to use a
control device other than one specified in this subpart that has not
been approved by the Administrator, as required by Sec. 63.743(c).
* * * * *
(d) Organic HAP and VOC content levels--primer, topcoat and
specialty coating application operations --
* * * * *
(4) The topcoat or specialty coating application operation is
considered in compliance when the conditions
[[Page 8434]]
specified in paragraphs (d)(4)(i) through (iv) of this section, as
applicable, and in paragraph (e) of this section are met. Failure to
meet any of the conditions identified in these paragraphs shall
constitute noncompliance.
(i) The topcoat application operation is considered in compliance
when the conditions specified in paragraphs (d)(4)(i)(A) are met. The
specialty coating application operation is considered in compliance
when the conditions specified in paragraphs (d)(4)(i)(B) are met.
(A) For all uncontrolled topcoats, all values of Hi and
Ha (as determined using the procedures specified in Sec.
63.750(c) and (d)) are less than or equal to 420 grams organic HAP per
liter (3.5 lb/gal) of topcoat (less water) as applied, and all values
of Gi and Ga (as determined using the procedures
specified in Sec. 63.750(e) and (f)) are less than or equal to 420
grams organic VOC per liter (3.5 lb/gal) of topcoat (less water and
exempt solvents) as applied.
(B) For all uncontrolled specialty coatings, all values of
Hi and Ha (as determined using the procedures
specified in Sec. 63.750(c) and (d)) are less than or equal to the HAP
content limits specified in Table 1 to Sec. 63.745 for the applicable
specialty coating types (less water) as applied, and all values of
Gi and Ga (as determined using the procedures
specified in Sec. 63.750(e) and (f)) are less than or equal to the VOC
content limits specified in Table 1 to Sec. 63.745 for the applicable
specialty coating types (less water and exempt solvents) as applied.
* * * * *
(e) Inorganic HAP emissions--primer, topcoat and specialty coating
application operations. For each primer, topcoat or specialty coating
application operation that emits inorganic HAP, the operation is in
compliance when:
* * * * *
(j) Performance tests shall be conducted under such conditions as
the Administrator specifies to the owner or operator based on
representative performance of the affected source for the period being
tested. Representative conditions exclude periods of startup and
shutdown unless specified by the Administrator or an applicable
subpart. The owner or operator may not conduct performance tests during
periods of malfunction. The owner or operator must record the process
information that is necessary to document operating conditions during
the test and include in such record an explanation to support that such
conditions represent normal operation. Upon request, the owner or
operator shall make available to the Administrator such records as may
be necessary to determine the conditions of performance tests.
0
9. Section 63.750 is amended by:
0
a. Revising paragraphs (c) introductory text, (d) introductory text and
(e) introductory text;
0
b. Revising paragraphs (f) introductory text and (f)(1)(iii);
0
c. Revising paragraph (h)(3)(i)(1); and
0
d. Revising paragraphs (k) introductory text, (m) introductory text and
(o).
The revisions are as follows:
Sec. 63.750 Test methods and procedures.
* * * * *
(c) Organic HAP content level determination--compliant primers,
topcoats and specialty coatings. For those uncontrolled primers,
topcoats and specialty coatings complying with the primer, topcoat or
specialty coating organic HAP content limits specified in Sec.
63.745(c) without being averaged, the procedures in paragraphs (c)(1)
through (3) of this section shall be used to determine the mass of
organic HAP emitted per volume of coating (less water) as applied. As
an alternative to the procedures in paragraphs (c)(1) through (3) of
this section, an owner or operator may use the coating manufacturer's
supplied data to demonstrate that organic HAP emitted per volume of
coating (less water), as applied, is less than or equal to the
applicable organic HAP limit specified in Sec. 63.745(c).
* * * * *
(d) Organic HAP content level determination--averaged primers,
topcoats and specialty coatings. For those uncontrolled primers,
topcoats and specialty coatings that are averaged together in order to
comply with the primer, topcoat and specialty coating organic HAP
content limits specified in Sec. 63.745(c), the following procedure
shall be used to determine the monthly volume-weighted average mass of
organic HAP emitted per volume of coating (less water) as applied,
unless the permitting agency specifies a shorter averaging period as
part of an ambient ozone control program.
* * * * *
(e) VOC content level determination--compliant primers, topcoats
and specialty coatings. For those uncontrolled primers, topcoats and
specialty coatings complying with the primer, topcoat and specialty
coating VOC content levels specified in Sec. 63.745(c) without being
averaged, the procedures in paragraphs (e)(1) through (3) of this
section shall be used to determine the mass of VOC emitted per volume
of coating (less water and exempt solvents) as applied. As an
alternative to the procedures in paragraphs (e)(1) through (3) of this
section, an owner or operator may use coating manufacturer's supplied
data to demonstrate that VOC emitted per volume of coating (less water
and exempt solvents), as applied, is less than or equal to the
applicable VOC limit specified in Sec. 63.745(c).
* * * * *
(f) VOC content level determination--averaged primers, topcoats and
specialty coatings. For those uncontrolled primers, topcoats and
specialty coatings that are averaged within their respective coating
category in order to comply with the primer, topcoat and specialty
coating VOC content limits specified in Sec. 63.745 (c)(2), (4), and
(6), the following procedure shall be used to determine the monthly
volume-weighted average mass of VOC emitted per volume of coating (less
water and exempt solvents) as applied, unless the permitting agency
specifies a shorter averaging period as part of an ambient ozone
control program.
(1) * * *
(iii) Determine the VOC content of each primer, topcoat and
specialty coating formulation (less water and exempt solvents) as
applied using EPA Method 24 or from manufacturer's data.
* * * * *
(h) * * *
(3) * * *
(i)(1) Alternative application method--primers, topcoats and
specialty coatings. Each owner or operator seeking to use an
alternative application method (as allowed in Sec. 63.745(f)(1)(ix))
in complying with the standards for primers, topcoats and specialty
coatings shall use the procedures specified in paragraphs (i)(2)(i) and
(ii) or (iii) of this section to determine the organic HAP and VOC
emission levels of the alternative application technique as compared to
either HVLP or electrostatic spray application methods.
* * * * *
(k) Organic HAP content level determination--compliant chemical
milling maskants. For those uncontrolled chemical milling maskants
complying with the chemical milling maskant organic HAP content limit
specified in Sec. 63.747(c)(1) without being averaged, the procedure
in paragraph (k)(1) of this section shall be used to determine the mass
of organic HAP emitted per unit volume of coating (chemical milling
maskant) i as applied (less water), Hi (lb/gal). As an
alternative
[[Page 8435]]
to the procedures in paragraph (k)(1) of this section, an owner or
operator may use coating manufacturer's supplied data to demonstrate
that organic HAP emitted per volume of coating (less water), as
applied, is less than or equal to the applicable organic HAP limit
specified in Sec. 63.747(c).
* * * * *
(m) VOC content level determination--compliant chemical milling
maskants. For those uncontrolled chemical milling maskants complying
with the chemical milling maskant VOC content limit specified in Sec.
63.747(c)(2) without being averaged, the procedure specified in
paragraphs (m)(1) and (2) of this section shall be used to determine
the mass of VOC emitted per volume of chemical milling maskant (less
water and exempt solvents) as applied. As an alternative to the
procedures in paragraphs (m)(1) and (2) of this section, an owner or
operator may use coating manufacturer's supplied data to demonstrate
that VOC emitted per volume of coating (less water and exempt
solvents), as applied, is less than or equal to the applicable VOC
limit specified in Sec. 63.747(c).
* * * * *
(o) Inorganic HAP emissions--dry particulate filter certification
requirements. Dry particulate filters used to comply with Sec.
63.745(g)(2) or Sec. 63.746(b)(4) must be certified by the filter
manufacturer or distributor, paint/depainting booth supplier and/or the
facility owner or operator using method 319 in appendix A of this part,
to meet or exceed the efficiency data points found in Tables 2 and 3 or
4 and 5 of Sec. 63.745 for existing or new sources respectively.
0
10. Section 63.751 is amended by revising paragraph (c) to read as
follows:
Sec. 63.751 Monitoring requirements.
* * * * *
(c) Dry particulate filter, HEPA filter and waterwash systems--
primer, topcoat and specialty coating application operations. (1) Each
owner or operator using a dry particulate filter system to meet the
requirements of Sec. 63.745(g)(2) shall, while primer, topcoat and
specialty coating application operations are occurring, continuously
monitor the pressure drop across the system and read and record the
pressure drop once per shift following the recordkeeping requirements
of Sec. 63.752(d).
(2) Each owner or operator using a conventional waterwash system to
meet the requirements of Sec. 63.745(g)(2) shall, while primer or
topcoat application operations are occurring, continuously monitor the
water flow rate through the system and read and record the water flow
rate once per shift following the recordkeeping requirements of Sec.
63.752(d). Each owner or operator using a pumpless waterwash system to
meet the requirements of Sec. 63.745(g)(2) shall, while primer,
topcoat and specialty coating application operations are occurring,
measure and record the parameter(s) recommended by the booth
manufacturer that indicate booth performance once per shift, following
the recordkeeping requirements of Sec. 63.752(d).
* * * * *
0
11. Section 63.752 is amended by:
0
a. Revising paragraph (a);
0
b. Revising paragraphs (c) introductory text, (c)(1), (c)(2)
introductory text, (c)(4) introductory text, (c)(5) introductory text
and (c)(6) introductory text;
0
c. Revising paragraphs (d) paragraph heading and (d)(1); and
0
d. Revising paragraph (f) introductory text.
The revisions read as follows:
Sec. 63.752 Recordkeeping requirements.
(a) General. Each owner or operator of a source subject to this
subpart shall fulfill all recordkeeping requirements specified in Sec.
63.10 (a), (b), (d) and (f), except Sec. 63.10(b)(2)(i), (iv), and
(v). Each owner or operator must also record and maintain according to
Sec. 63.10(b)(1) the information specified in paragraph (a)(1) through
(3) of this section.
(1) In the event that an affected unit fails to meet an applicable
standard, record the number of failures. For each failure record the
date, time and duration of each failure.
(2) For each failure to meet an applicable standard, record and
retain a list of the affected sources or equipment, an estimate of the
quantity of each regulated pollutant emitted over any emission limit
and a description of the method used to estimate the emissions.
(3) Record actions taken to minimize emissions in accordance with
Sec. 63.743(e), and any corrective actions taken to return the
affected unit to its normal or usual manner of operation.
* * * * *
(c) Primer, topcoat and specialty coating application operations--
organic HAP and VOC. Each owner or operator required to comply with the
organic HAP and VOC content limits specified in Sec. 63.745(c) shall
record the information specified in paragraphs (c)(1) through (6) of
this section, as appropriate. Each owner and operator using coating
manufacturer's supplied data to demonstrate compliance with the
applicable organic HAP or VOC limit specified in Sec. 63.745(c) may
retain the manufacturer's documentation and annual purchase records in
place of the records specified in paragraphs (c)(2) and (3) of this
section.
(1) The name and VOC content as received and as applied of each
primer, topcoat and specialty coating used at the facility.
(2) For uncontrolled primers, topcoats and specialty coatings that
meet the organic HAP and VOC content limits in Sec. 63.745(c)(1)
through (6) without averaging:
* * * * *
(4) For primers, topcoats and specialty coatings complying with the
organic HAP or VOC content level by averaging:
* * * * *
(5) For primers, topcoats and specialty coatings that are
controlled by a control device other than a carbon adsorber:
* * * * *
(6) For primers, topcoats and specialty coatings that are
controlled by a carbon adsorber:
* * * * *
(d) Primer, topcoat and specialty coating application operations--
inorganic HAP emissions. (1) Each owner or operator complying with
Sec. 63.745(g) for the control of inorganic HAP emissions from primer,
topcoat and specialty coating application operations through the use of
a dry particulate filter system or a HEPA filter system shall record
the pressure drop across the operating system once each shift during
which coating operations occur.
(f) Chemical milling maskant application operations. Each owner or
operator seeking to comply with the organic HAP and VOC content limits
for the chemical milling maskant application operation, as specified in
Sec. 63.747(c), or the control system requirements specified in Sec.
63.747(d), shall record the information specified in paragraphs (f)(1)
through (4) of this section, as appropriate. Each owner and operator
using coating manufacturer's supplied data to demonstrate compliance
with the applicable organic HAP or VOC limit specified in Sec.
63.747(c) may retain the manufacturer's documentation and annual
purchase records in place of the records specified in paragraph (f)(1)
of this section.
* * * * *
0
12. Section 63.753 is amended by:
0
a. Revising paragraph (a)(1) introductory text and (a)(2);
0
b. Adding paragraphs (a)(4) and (5);
0
c. Revising paragraphs (c) introductory text, (c)(1)(i) and (ii).
[[Page 8436]]
0
d. Revising paragraph (e)(1).
The revisions and additions read as follows:
Sec. 63.753 Reporting requirements.
(a)(1) Except as provided in paragraphs (a)(2) through (5) of this
section, each owner or operator subject to this subpart shall fulfill
the requirements contained in Sec. 63.9(a) through (e) and (h) through
(j), Notification requirements and Sec. 63.10(a), (b), (d) and (f),
Recordkeeping and reporting requirements, of the General Provisions, 40
CFR part 63, subpart A and that the initial notification for existing
sources required in Sec. 63.9(b)(2) shall be submitted not later than
September 1, 1997, or as specified in Sec. 63.9(b)(2). In addition to
the requirements of Sec. 63.9(h), the notification of compliance
status shall include:
* * * * *
(2) The initial notification for existing sources, required in
Sec. 63.9(b)(2) shall be submitted no later than September 1, 1997, or
as specified in Sec. 63.9(b)(2). For the purposes of this subpart, a
title V or part 70 permit application may be used in lieu of the
initial notification required under Sec. 63.9(b)(2), provided the same
information is contained in the permit application as required by Sec.
63.9(b)(2), and the State to which the permit application has been
submitted has an approved operating permit program under part 70 of
this chapter and has received delegation of authority from the EPA.
Permit applications shall be submitted by the same due dates as those
specified for the initial notifications.
* * * * *
(4) Each owner or operator subject to this subpart is not required
to comply with Sec. 63.10(b)(2)(i), (b)(2)(iv), (b)(2)(v), and (d)(5).
(5) If a source fails to meet an applicable standard specified in
Sec. Sec. 63.744 through 63.748, report such events in the semiannual
report:
(i) The number of failures to meet an applicable standard.
(ii) For each instance, report the date, time and duration of each
failure.
(iii) For each failure the report must include a list of the
affected sources or equipment, an estimate of the quantity of each
regulated pollutant emitted over any emission limit and a description
of the method used to estimate the emissions.
* * * * *
(c) Primer, topcoat and specialty coating application operations.
Each owner or operator of a primer or topcoat application operation
subject to this subpart shall submit the following information:
(1) * * *
(i) For primers, topcoats and specialty coatings where compliance
is not being achieved through the use of averaging or a control device,
the HAP or VOC content in manufacturer's supplied data as recorded
under Sec. 63.752(c), or each value of Hi and Gi
as recorded under Sec. 63.752(c)(2)(i), that exceeds the applicable
organic HAP or VOC content limit specified in Sec. 63.745(c);
(ii) For primers, topcoats and specialty coatings where compliance
is being achieved through the use of averaging, each value of
Ha and Ga, as recorded under Sec.
63.752(c)(4)(i), that exceeds the applicable organic HAP or VOC content
limit specified in Sec. 63.745(c);
* * * * *
(e) * * *
(1) For chemical milling maskants where compliance is not being
achieved through the use of averaging or a control device, the HAP or
VOC content in manufacturer's supplied data as recorded under Sec.
63.752(f), or each value of Hi and Gi as recorded
under Sec. 63.752(f)(1)(i), that exceeds the applicable organic HAP or
VOC content limit specified in Sec. 63.747(c);
* * * * *
0
13. Revise Table 1 to Subpart GG of Part 63 to read as follows:
Table 1 to Subpart GG of Part 63--General Provisions Applicability to
Subpart GG
------------------------------------------------------------------------
Applies to
Reference affected sources Comment
in subpart GG
------------------------------------------------------------------------
63.1(a)(1).................... Yes. .....................
63.1(a)(2).................... Yes. .....................
63.1(a)(3).................... Yes. .....................
63.1(a)(4).................... Yes. .....................
63.1(a)(5).................... No............... Reserved.
63.1(a)(6).................... Yes. .....................
63.1(a)(7).................... Yes. .....................
63.1(a)(8).................... Yes. .....................
63.1(a)(9).................... No............... Reserved.
63.1(a)(10)................... Yes. .....................
63.1(a)(11)................... Yes. .....................
63.1(a)(12)................... Yes. .....................
63.1(a)(13)................... Yes. .....................
63.1(a)(14)................... Yes. .....................
63.1(b)(1).................... Yes. .....................
63.1(b)(2).................... Yes. .....................
63.1(b)(3).................... Yes. .....................
63.1(c)(1).................... Yes. .....................
63.1(c)(2).................... Yes.............. Subpart GG does not
apply to area
sources.
63.1(c)(3).................... No............... Reserved.
63.1(c)(4).................... Yes. .....................
63.1(c)(5).................... Yes. .....................
63.1(d)....................... No............... Reserved.
63.1(e)....................... Yes. .....................
63.2.......................... Yes. .....................
63.3.......................... Yes. .....................
63.4(a)(1).................... Yes. .....................
63.4(a)(2).................... Yes. .....................
63.4(a)(3).................... Yes. .....................
63.4(a)(4).................... No............... Reserved.
63.4(a)(5).................... Yes. .....................
[[Page 8437]]
63.4(b)....................... Yes. .....................
63.4(c)....................... Yes. .....................
63.5(a)....................... Yes. .....................
63.5(b)(1).................... Yes. .....................
63.5(b)(2).................... No............... Reserved.
63.5(b)(3).................... Yes. .....................
63.5(b)(4).................... Yes. .....................
63.5(b)(5).................... Yes. .....................
63.5(b)(6).................... Yes. .....................
63.5(c)....................... No............... Reserved.
63.5(d)(1)(i)................. Yes. .....................
63.5(d)(1)(ii)(A) through (H). Yes. .....................
63.5(d)(1)(ii)(I)............. No............... Reserved.
63.5(d)(1)(ii)(J)............. Yes. .....................
63.5(d)(1)(iii)............... Yes. .....................
63.5(d)(2) through (4)........ Yes. .....................
63.5(e)....................... Yes. .....................
63.5(f)....................... Yes. .....................
63.6(a)....................... Yes. .....................
63.6(b)(1) through (5)........ Yes.............. Sec. 63.749(a)
specifies compliance
dates for new
sources.
63.6(b)(6).................... No............... Reserved.
63.6(b)(7).................... Yes. .....................
63.6(c)(1).................... Yes. .....................
63.6(c)(2).................... No............... The standards in
subpart GG are
promulgated under
section 112(d) of
the CAA.
63.6(c)(3) and (4)............ No............... Reserved.
63.6(c)(5).................... Yes. .....................
63.6(d)....................... No............... Reserved.
63.6(e)(1)(i)................. No............... See Sec. 63.743(e)
for general duty
requirement.
63.6(e)(1)(ii)................ No. .....................
63.6(e)(2).................... No............... Section reserved.
63.6(e)(3).................... No. .....................
63.6(f)(1).................... No. .....................
63.6(f)(2) and (3)............ Yes. .....................
63.6(g)....................... Yes. .....................
63.6(h)....................... No............... The standards in
subpart GG do not
include opacity
standards.
63.6(i)(1) and (3)............ Yes. .....................
63.6(i)(4)(i)(A).............. Yes. .....................
63.6(i)(4)(i)(B).............. No............... Sec. 63.743(a)(4)
specifies that
requests for
extension of
compliance must be
submitted no later
than 120 days before
an affected source's
compliance date.
63.6(i)(4)(ii)................ No............... The standards in
subpart GG are
promulgated under
section 112(d) of
the CAA.
63.6(i)(5) through (12)....... Yes. .....................
63.6(i)(13)................... Yes. .....................
63.6(i)(14)................... Yes. .....................
63.6(i)(15)................... No............... Reserved.
63.6(i)(16)................... Yes. .....................
63.6(j)....................... Yes. .....................
63.7(a)(1).................... Yes. .....................
63.7(a)(2)(i) through (vi).... Yes. .....................
63.7(a)(2)(vii) and (viii).... No............... Reserved.
63.7(a)(2)(ix)................ Yes. .....................
63.7(a)(3).................... Yes. .....................
63.7(b)....................... Yes. .....................
63.7(c)....................... Yes. .....................
63.7(d)....................... Yes. .....................
63.7(e)(1).................... No............... See Sec. 63.749(j).
63.7(e)(2) through (4)........ Yes. .....................
63.7(f)....................... Yes. .....................
63.7(g)(1).................... Yes. .....................
63.7(g)(2).................... No............... Reserved.
63.7(g)(3).................... Yes. .....................
63.7(h)....................... Yes. .....................
63.8(a)(1) and (2)............ Yes. .....................
63.8(a)(3).................... No............... Reserved.
63.8(a)(4).................... Yes. .....................
63.8(b)....................... Yes. .....................
63.8(c)(1)(i)................. No. .....................
[[Page 8438]]
63.8(c)(1)(ii)................ Yes. .....................
63.8(c)(1)(iii)............... No. .....................
63.8(c)(2) through (d)(2)..... Yes. .....................
63.8(d)(3).................... No. .....................
63.8(e)(1) through (4)........ Yes. .....................
63.8(e)(5)(i)................. Yes. .....................
63.8(e)(5)(ii)................ No............... The standards in
subpart GG do not
include opacity
standards.
63.8(f)(1).................... Yes. .....................
63.8(f)(2)(i) through (vii)... Yes. .....................
63.8(f)(2)(viii).............. No............... The standards in
subpart GG do not
include opacity
standards.
63.8(f)(2)(ix)................ Yes. .....................
63.8(f)(3) through (6)........ Yes. .....................
63.8(g)....................... Yes. .....................
63.9(a)....................... Yes. .....................
63.9(b)(1).................... Yes. .....................
63.9(b)(2).................... Yes.............. Sec. 63.753(a)(1)
requires submittal
of the initial
notification at
least 1 year prior
to the compliance
date; Sec.
63.753(a)(2) allows
a title V or part 70
permit application
to be substituted
for the initial
notification in
certain
circumstances.
63.9(b)(3).................... Yes. .....................
63.9(b)(4).................... Yes. .....................
63.9(b)(5).................... Yes. .....................
63.9(c)....................... Yes. .....................
63.9(d)....................... Yes. .....................
63.9(e)....................... Yes. .....................
63.9(f)....................... No............... The standards in
subpart GG do not
include opacity
standards.
63.9(g)(1).................... No. .....................
63.9(g)(2).................... No............... The standards in
subpart GG do not
include opacity
standards.
63.9(g)(3).................... No. .....................
63.9(h)(1) through (3)........ Yes.............. Sec. 63.753(a)(1)
also specifies
additional
information to be
included in the
notification of
compliance status.
63.9(h)(4).................... No............... Reserved.
63.9(h)(5) and (6)............ Yes. .....................
63.9(i)....................... Yes. .....................
63.9(j)....................... Yes. .....................
63.10(a)...................... Yes. .....................
63.10(b)(1)................... Yes. .....................
63.10(b)(2)(i)................ No. .....................
63.10(b)(2)(ii)............... No............... See Sec. 63.752(a)
for recordkeeping
of: (1) Date, time
and duration; (2)
Listing of affected
source or equipment
and an estimate of
the quantity of each
regulated pollutant
emitted over the
standard; and (3)
Actions to minimize
emissions and
correct the failure.
63.10(b)(2)(iii).............. Yes. .....................
63.10(b)(2)(iv) and (v)....... No. .....................
63.10(b)(2)(vi)............... Yes. .....................
63.10(b)(2)(vi)(A) through (C) No............... Sec.
63.10(b)(vii)(A),
(B) and (C) do not
apply because
subpart GG does not
require the use of
CEMS.
63.10(b)(2)(vii) through (xiv)
63.10(b)(3)................... Yes. .....................
63.10(c)(1)................... No. .....................
63.10(c)(2) through (4)....... No............... Reserved.
63.10(c)(5) and (6)........... No. .....................
63.10(c)(7) and (8)........... Yes. .....................
63.10(c)(9)................... No............... Reserved.
63.10(c)(10) through (13)..... No. .....................
63.10(c)(14).................. No............... Sec. 63.8(d) does
not apply to this
subpart.
63.10(c)(15).................. No. .....................
63.10(d)(1) and (2)........... Yes. .....................
63.10(d)(3)................... No............... The standards in
subpart GG do not
include opacity
standards.
63.10(d)(4)................... Yes. .....................
63.10(d)(5)................... No. See Sec. .....................
63.753 (a)(5)
for malfunction
reporting
requirements..
63.(10)(e)(1)................. No. .....................
[[Page 8439]]
63.10(e)(2)(i)................ No. .....................
63.10(e)(2)(ii)............... No............... The standards in
subpart GG do not
include opacity
standards.
63.10(e)(3)................... No. .....................
63.10(e)(4)................... No............... The standards in
subpart GG do not
include opacity
standards.
63.10(f)...................... Yes. .....................
63.11......................... Yes. .....................
63.12......................... Yes. .....................
63.13......................... Yes. .....................
63.14......................... Yes. .....................
63.15......................... Yes. .....................
63.16......................... Yes.
------------------------------------------------------------------------
[FR Doc. 2015-02055 Filed 2-13-15; 8:45 am]
BILLING CODE 6560-50-P