Standards of Performance for Petroleum Refineries; Standards of Performance for Petroleum Refineries for Which Construction, Reconstruction, or Modification Commenced After May 14, 2007, 56421-56480 [2012-20866]
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Vol. 77
Wednesday,
No. 177
September 12, 2012
Part III
Environmental Protection Agency
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40 CFR Parts 9 and 60
Standards of Performance for Petroleum Refineries; Standards of
Performance for Petroleum Refineries for Which Construction,
Reconstruction, or Modification Commenced After May 14, 2007; Final Rule
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Parts 9 and 60
[EPA–HQ–OAR–2007–0011; FRL–9672–3]
RIN 2060–AN72
Standards of Performance for
Petroleum Refineries; Standards of
Performance for Petroleum Refineries
for Which Construction,
Reconstruction, or Modification
Commenced After May 14, 2007
Environmental Protection
Agency (EPA).
ACTION: Final rule; lift stay of effective
date.
AGENCY:
On June 24, 2008, the EPA
promulgated amendments to the
Standards of Performance for Petroleum
Refineries and new standards of
performance for petroleum refinery
process units constructed, reconstructed
or modified after May 14, 2007. The
EPA subsequently received three
petitions for reconsideration of these
final rules. On September 26, 2008, the
EPA granted reconsideration and issued
a stay for the issues raised in the
petitions regarding process heaters and
flares. On December 22, 2008, the EPA
addressed those specific issues by
proposing amendments to certain
provisions for process heaters and flares
and extending the stay of these
provisions until further notice. The EPA
also proposed technical corrections to
the rules for issues that were raised in
the petitions for reconsideration. In this
action, the EPA is finalizing those
amendments and technical corrections
and is lifting the stay of all the
provisions granted on September 26,
2008 and extended until further notice
on December 22, 2008.
DATES: The stay of the definition of
‘‘flare’’ in 40 CFR 60.101a, paragraph (g)
of 40 CFR 60.102a, and paragraphs (d)
and (e) of 40 CFR 60.107a is lifted and
this final rule is effective on November
13, 2012. The incorporation by reference
SUMMARY:
of certain publications listed in the final
rule is approved by the Director of the
Federal Register as of November 13,
2012.
ADDRESSES: The EPA has established a
docket for this action under Docket ID
No. EPA–HQ–OAR–2007–0011. All
documents in the docket are listed in
the www.regulations.gov index.
Although listed in the index, some
information is not publicly available,
e.g., confidential business information
(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 form.
Publicly available docket materials are
available either electronically in
www.regulations.gov or in hard copy at
the EPA Docket Center, Standards of
Performance for Petroleum Refineries
Docket, EPA West Building, Room 3334,
1301 Constitution Ave. NW.,
Washington, DC. The Public Reading
Room is open from 8:30 a.m. to 4:30
p.m., Monday through Friday, excluding
legal holidays. The telephone number
for the Public Reading Room is (202)
566–1744, and the telephone number for
the Air Docket is (202) 566–1742.
FOR FURTHER INFORMATION CONTACT: Ms.
Brenda Shine, Office of Air Quality
Planning and Standards, Sector Policies
and Programs Division, Refining and
Chemicals Group (E143–01),
Environmental Protection Agency,
Research Triangle Park, NC 27711,
telephone number: (919) 541–3608; fax
number: (919) 541–0246; email address:
shine.brenda@epa.gov.
SUPPLEMENTARY INFORMATION: 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?
C. Judicial Review
II. Background Information
A. Executive Summary
B. Background of the Refinery NSPS
III. Summary of the Final Rules and Changes
Since Proposal
A. What are the final amendments to the
standards of performance for petroleum
refineries (40 CFR part 60, subpart J)?
B. What are the final amendments to the
standards of performance for process
heaters (40 CFR part 60, subpart Ja)?
C. What are the final amendments to the
standards of performance for flares (40
CFR part 60, subpart Ja)?
D. What are the final amendments to the
definitions in 40 CFR part 60, subpart Ja?
E. What are the final technical corrections
to 40 CFR part 60, subpart Ja?
IV. Summary of Significant Comments and
Responses
A. Process Heaters
B. Flares
C. Other Comments
V. Summary of Cost, Environmental, Energy
and Economic Impacts
A. What are the emission reduction and
cost impacts for the final amendments?
B. What are the economic impacts?
C. What are the benefits?
VI. 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
D. Unfunded Mandates Reform Act
E. Executive Order 13132: Federalism
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
G. Executive Order 13045: Protection of
Children From Environmental Health
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
J. Executive Order 12898: Federal Actions
To Address Environmental Justice in
Minority Populations and Low-Income
Populations
K. Congressional Review Act
I. General Information
A. Does this action apply to me?
Categories and entities potentially
regulated by these final rules include:
NAICS Code 1
Industry ...........................................................................................................................................
Federal government ........................................................................................................................
State/local/tribal government ..........................................................................................................
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Category
32411
............................
............................
1 North
Examples of regulated
entities
Petroleum refiners.
Not affected.
Not affected.
American Industry Classification System.
This table is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
regulated by this action. To determine
whether your facility would be
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regulated by this action, you should
examine the applicability criteria in 40
CFR 60.100 and 40 CFR 60.100a. If you
have any questions regarding the
applicability of this action to a
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particular entity, contact the person
listed in the preceding FOR FURTHER
INFORMATION CONTACT section.
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B. Where can I get a copy of this
document?
In addition to being available in the
docket, an electronic copy of this final
action is available on the World Wide
Web (WWW) through the Technology
Transfer Network (TTN). Following
signature, a copy of this final action will
be posted on the TTN’s policy and
guidance page for newly proposed or
promulgated rules at https://
www.epa.gov/ttn/oarpg. The TTN
provides information and technology
exchange in various areas of air
pollution control.
The EPA has created a redline
document comparing the existing
regulatory text of 40 CFR part 60,
subpart Ja and the final amendments to
aid the public’s ability to understand
the changes to the regulatory text. This
document has been placed in the docket
for this rulemaking (Docket ID No. EPA–
HQ–OAR–2007–0011).
C. Judicial Review
Under section 307(b)(1) of the Clean
Air Act (CAA), judicial review of these
final rules is available only by filing a
petition for review in the United States
Court of Appeals for the District of
Columbia Circuit by November 13,
2012. Under section 307(b)(2) of the
CAA, the requirements established by
these final rules may not be challenged
separately in any civil or criminal
proceedings brought by the EPA to
enforce these requirements.
Section 307(d)(7)(B) of the CAA
further provides that ‘‘[o]nly an
objection to a rule or procedure which
was raised with reasonable specificity
during the period for public comment
(including any public hearing) may be
raised during judicial review.’’ This
section also provides a mechanism for
us to convene a proceeding for
reconsideration, ‘‘[i]f the person raising
an objection can demonstrate to the EPA
that it was impracticable to raise such
objection within [the period for public
comment] or if the grounds for such
objection arose after the period for
public comment (but within the time
specified for judicial review) and if such
objection is of central relevance to the
outcome of the rule.’’ Any person
seeking to make such a demonstration to
us should submit a Petition for
Reconsideration to the Office of the
Administrator, U.S. EPA, Room 3000,
Ariel Rios Building, 1200 Pennsylvania
Ave. NW., Washington, DC 20460, with
56423
a copy to both the person(s) listed in the
preceding FOR FURTHER INFORMATION
CONTACT section, and the Associate
General Counsel for the Air and
Radiation Law Office, Office of General
Counsel (Mail Code 2344A), U.S. EPA,
1200 Pennsylvania Ave. NW.,
Washington, DC 20460.
II. Background Information
A. Executive Summary
1. Purpose of the Regulatory Action
This action finalizes amendments that
were proposed on December 22, 2008, to
address reconsideration issues related to
the promulgation of new source
performance standards (NSPS) for flares
and process heaters on June 24, 2008.
This action also lifts the stay that was
granted on September 26, 2008 (73 FR
55751) and extended until further notice
on December 22, 2008 (73 FR 78552) on
the provisions at issue.
2. Summary of Major Provisions
Table 1 presents a summary of major
changes to the rule since it was first
promulgated on June 24, 2008. The
following discussion is a summary of
major provisions of this rule.
TABLE 1—SUMMARY OF MAJOR CHANGES SINCE JUNE 24, 2008, PROMULGATION
Aspect
NSPS Ja
(June 24, 2008)
NSPS Ja final
All Process Heater NOX limits .......
Natural Draft Process Heaters .......
Forced Draft Process Heaters .......
Forced Draft Process Heaters with
Co-fired (oil and gas) Burners.
Averaging time ..............................
NOX Emission Limits ....................
NOX Emission Limits ....................
NOX Emission Limits ....................
24-hour rolling average ................
40 ppmv ........................................
40 ppmv ........................................
40 ppmv ........................................
Natural Draft Process Heaters with
Co-fired (oil and gas) Burners.
NOX Emission Limits ....................
40 ppmv ........................................
Process Heaters ............................
Alternate Emission Standards ......
None .............................................
Flares .............................................
Applicability ...................................
H2S concentration limit .................
Flares .............................................
Compliance
flares.
New or reconstructed flare systems or existing flare systems
that are physically altered to increase flow or to add new connections.
162 ppmv H2S (3-hour average);
60 ppmv H2S (annual rolling average).
Comply with H2S limit at start-up,
and all other requirements within 1 year.
30-day rolling average.
40 ppmv or 0.04 lb/MM BTU.
60 ppmv or 0.06 lb/MM BTU.
150 ppmv or Weighted average
based on oil at 0.40 lb/MM BTU
and gas at 0.11 lb/MM BTU.
150 ppmv or weighted average
based on oil at 0.35 lb/MM BTU
and gas at 0.06 lb/MM BTU.
Case by case approval for some
circumstances.
Similar, except specific list of connections that do not trigger applicability.
Fuel gas combustion devices ........
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Affected source
Flares .............................................
Flow limits .....................................
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250,000 scfd.
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162 ppmv H2S (3-hour average);
No 60 ppmv H2S long term
concentration limit for flares.
Comply with H2S limit at start-up
(except for modified flares not
previously subject to the H2S
limit in 40 CFR part 60, subpart
J or those with monitoring alternatives, or those complying with
subpart J as specified in a consent decree, which comply no
later than 3 years) and all other
requirements within 3 years.
No limits.
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TABLE 1—SUMMARY OF MAJOR CHANGES SINCE JUNE 24, 2008, PROMULGATION—Continued
Aspect
NSPS Ja
(June 24, 2008)
NSPS Ja final
Flares .............................................
Root Cause Analysis and Corrective Action (RCA/CA).
Flow monitoring ............................
RCA/CA required on upsets or
malfunctions in excess of
500,000 scfd or 500 lbs/day
SO2 from SSM.
Continuous ....................................
RCA/CA required for 500,000 scfd
above base load and 500 lbs
SO2 in any 24-hour period.
Flares .............................................
Flares .............................................
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Affected source
Sulfur Monitoring ..........................
Affected process heaters are those that
were modified, reconstructed or
constructed after May 14, 2007. For
these affected sources, these final
amendments include concentrationbased nitrogen oxide (NOX) emissions
limits and alternative heating valuebased NOX emissions limits, both
determined daily on a 30-day rolling
average basis. These final amendments
establish limits of 40 parts per million
by volume (ppmv) NOX (or 0.04 pounds
per million British thermal units (lb/
MMBtu) and 60 ppmv NOX (or 0.06 lb/
MMBtu) for natural draft and forced
draft process heaters, respectively. Cofired process heaters, designed to
operate on gaseous and liquid fuel (e.g.,
oil), must meet either 150 ppmv NOX or
alternative heating value-based limits,
weighted based on oil and gas use. The
NSPS also contains an alternative
compliance option that allows owners
and operators to obtain EPA approval
for a site-specific NOX limit for process
heaters that may have difficulty meeting
the standards under certain situations.
These final amendments also include
monitoring, recordkeeping and
reporting requirements necessary to
demonstrate compliance with the NOX
emission standards.
For flares, these final amendments
define a flare as a separate affected
facility rather than a type of fuel gas
combustion device. As such, these final
amendments remove requirements for
flares to comply with the performance
standards for sulfur dioxide (SO2)
(expressed as a 162 ppmv short-term
hydrogen sulfide (H2S) concentration
limit) and, instead, establish a separate
suite of standards for flares. We are not
finalizing the requirement in the
December 22, 2008, proposed
amendments for flares to meet the longterm 60 ppmv H2S fuel gas
concentration limit. As explained in
section IV of this preamble, we
determined that requiring refineries to
ensure the fuel gas they send to their
flares meets a long-term H2S
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Continuous Total Reduced Sulfur
(TRS).
concentration of 60 ppmv is not
appropriate for flares.
Affected flares are those that were
modified, reconstructed or constructed
after June 24, 2008. In general, a flare is
modified if a connection is made into
the flare header that can increase
emissions from the flare. The NSPS
specifically identifies certain
connections to a flare that do not
constitute a modification of the flare
because they do not result in emissions
increases.
The final amendments for flares
include a suite of standards that apply
at all times. This suite of standards
requires refineries to: (1) Develop and
implement a flare management plan; (2)
conduct root cause analyses and take
corrective action when waste gas sent to
the flare exceeds a flow rate of 500,000
standard cubic feet per day (scfd) above
the baseline flow or contains sulfur that,
upon combustion, will emit more than
500 pounds (lb) of SO2 in a 24-hour
period; and (3) optimize management of
the fuel gas by limiting the short-term
concentration of H2S to 162 ppmv
during normal operating conditions.
The final amendments require that
flares be equipped with flow and sulfur
monitors except in cases where flares
are used infrequently or are configured
such that they cannot receive high
sulfur gas. For flares that are configured
such that they only receive inherently
low sulfur gas streams, continuous
sulfur monitors are not necessary
because a root cause analysis will be
triggered by an exceedance of the flow
rate threshold long before they exceed
the 500 lb SO2 trigger in a 24-hour
period.
For infrequently used flares, the NSPS
allows for less burdensome monitoring,
consisting of monitoring the differential
pressure between the flare header and
the flare water seal to determine if a gas
release to the flare has occurred. Any
instance where the pressure upstream of
the water seal (expressed in inches of
water) exceeds the water seal height
triggers a requirement to perform a root
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Continuous except for intermittent/
emergency only flares with
water seal monitoring and limited releases.
Continuous TRS, using reference
method 15A (Total Sulfur).
cause analysis and corrective action
analysis, unless the discharge is related
to flare gas recovery system compressor
cycling or a planned startup or
shutdown (of a refinery process unit or
ancillary equipment connected to the
flare) following the procedures in the
flare management plan. The NSPS also
contains an alternative compliance
option for refinery flares located in the
South Coast Air Quality Management
District (SCAQMD) or the Bay Area Air
Quality Management District
(BAAQMD). An affected flare subject to
40 CFR part 60, subpart Ja may elect to
comply with SCAQMD Rule 1118 or
both BAAQMD Regulation 12, Rule 11
and BAAQMD Regulation 12, Rule 12 as
an alternative to complying with the
requirements of subpart Ja.
3. Costs and Benefits
The provisions for flares and other
fuel gas combustion devices (i.e.,
process heaters and boilers) from the
final June 2008 standards were stayed.
The analysis for this final rule includes
the same unit costs for the flare
provisions as the final June 2008 rule
but reflects recalculated total costs using
data collected in the March 2011
information collection request (ICR) to
update the number of flares. For the
June 2008 standards, we estimated that
40 flares would be affected. We now
anticipate that there will be 400 affected
flares that will be subject to this final
rule. Table 2 includes the recalculated
cost estimates based on the updated
number of flares since 2008, broken out
by specific flare requirements. For the
other fuel gas combustion devices, the
total annualized costs for those
provisions were estimated at $24
million (2006 dollars) in the June 2008
rule and remain the same. As discussed
below, because there are no additional
incremental costs associated with the
other fuel gas combustion device
provisions, we consider those annual
costs accounted for in the final June
2008 standards. We are presenting these
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costs and benefits here again, even
though we estimate no changes to them,
since these provisions will become
effective upon this final action to lift the
stay on certain provisions in the June
2008 rule. For the June 2008 rule, we
estimated the benefits to be $220
million to $1.9 billion and $200 to $1.7
billion at a 3-percent discount rate and
7-percent discount rate, respectively.1
Cost impacts for flares are presented
in Table 2. The estimated total capital
cost of complying with the final
amendments to 40 CFR part 60, subpart
Ja for flares is $460 million dollars (2006
dollars). The estimated annual cost,
including annualized capital costs, is a
cost savings of about $79 million (2006
dollars) due to the replacement of some
natural gas purchases with recovered
flare gas and the retention of
intermediate and product streams due to
a reduction in the number of
malfunctions associated with refinery
process units and ancillary equipment
connected to the flare. Note that not all
refiners will realize a cost savings since
we only estimate that refineries with
high flare flows will install vapor
recovery systems. Although the rule
does not specifically require installation
of flare gas recovery systems, we project
that owners and operators of flares
receiving high waste gas flows will
conclude, upon installation of monitors,
implementation of their flare
management plans, and implementation
of root causes analyses, that installing
flare gas recovery would result in fuel
savings by using the recovered flare gas
where purchased natural gas is now
being used to fire equipment such as
boilers and process heaters. The flare
management plan requires refiners to
conduct a thorough review of the flare
system so that flare gas recovery systems
are installed and used where these
systems are warranted. As part of the
development of the flare management
plan, refinery owners and operators
must provide rationale and supporting
evidence regarding the flare waste gas
reduction options considered. In
addition, consistent with Executive
Order 13563 (Improving Regulation and
Regulatory Review, issued on January
18, 2011), for facilities implementing
flare gas recovery, we are finalizing
56425
provisions that would allow the owner
or operator to reduce monitoring costs
and the number of root cause analyses,
corrective actions, and corresponding
recordkeeping and reporting they would
need to perform. The costs calculated
for this rule, however, do not account
for potential savings due to these
provisions (reduced monitoring, root
cause analysis, etc.). We estimate that
the final requirements for flares will
reduce emissions of SO2 by 3,200 tons
per year (tons/yr), NOX by 1,100 tons/
yr and volatile organic compounds
(VOC) by 3,400 tons/yr from the
baseline. The overall cost effectiveness
is a cost savings of about $10,000 per
ton of combined pollutants removed.
We also estimate that the final
requirements for flares will result in
emissions reduction co-benefits of CO2
equivalents by 1,900,000 metric tonnes
per year, predominantly as a result of
our estimate of the largest flares
employing flare gas recovery, and to a
lesser extent, as a result of the flow rate
root cause analyses and corrective
actions applicable to all flares.
TABLE 2—COST IMPACTS FOR PETROLEUM REFINERY FLARES SUBJECT TO AMENDED STANDARDS UNDER 40 CFR PART
60, SUBPART JA
[Fifth year after the effective date of these final rule amendments]
Subpart Ja requirements
Total annual
cost without
credit
($1,000/yr)
Total capital
cost
($1,000)
Natural gas
offset/product
recovery credit
($1,000)
Total annual
cost
($1,000/yr)
Annual
emission
reductions
(tons SO2/yr)
Annual
emission
reductions
(tons NOX/yr)
Annual
emission
reductions
(tons VOC/yr)
Cost
effectiveness
($/ton emissions reduced)
Majority of flares (approximately 360 flares)
Flare Monitoring ..........................
Flare gas recovery ......................
Flare Management ......................
SO2 RCA/CA ...............................
Flowrate RCA/CA ........................
72,000
0
0
0
......................
12,000
0
790
1,900
900
0
0
0
0
(6,700)
12,000
0
790
1,900
(5,800)
0
0
0
2,600
3.4
0
0
0
0
50
0
0
270
0
390
........................
........................
2,900
760
(13,000)
Subtotal 1 ..............................
72,000
16,000
(6,700)
9,000
2,600
50
660
2,700
Largest flares (approximately 40 flares) 2
Flare Monitoring ..........................
Flare gas recovery ......................
Flare Management ......................
SO2 RCA/CA ...............................
Flowrate RCA/CA ........................
12,000
380,000
0
0
0
2,000
78,000
88
220
100
0
(170,000)
0
0
(740)
2,000
(90,000)
88
220
(640)
0
380
0
290
0.4
0
1,100
0
0
6
0
2,700
30
0
43
........................
(22,000)
2,900
760
(13,000)
Subtotal 1 ..............................
390,000
81,000
(170,000)
(88,000)
660
1,100
2,800
(20,000)
460,000
96,000
(180,000)
(79,000)
3,200
1,100
3,400
(10,000)
Total 1
............................
1 All
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estimates are rounded to two significant figures so numbers may not sum down columns.
2 The EPA has conducted an alternative analysis that presents the costs and benefits of the rule assuming that no refiners will opt to install flare gas recovery systems as part of their flare management strategy. This analysis is presented in the Regulatory Impact Analysis in the discussion provided in the executive summary
and in Section 4.1, available in the docket for this rulemaking.
We estimate the monetized benefits of
this final regulatory action for all flares
to be $260 million to $580 million (3percent discount rate) and $240 million
to $520 million (7-percent discount rate
for health benefits and 3-percent
discount rate for climate benefits). For
small flares only, we estimate the
monetized benefits are $170 million to
$410 million (3-percent discount rate)
and $150 million to $370 million (7percent discount rate for health benefits
1 It is important to note that the EPA has
implemented several substantial changes to the
benefits methodology since 2008, which makes it
challenging to compare the benefits of the June
2008 rule to the benefits of the current rulemaking.
The changes with the largest impact on the range
of monetized benefits are the removal of the
assumption of a threshold in the concentrationresponse function, the revision of the value-of-astatistical-life, and the range of risk estimates from
epidemiology studies rather than the range of risk
estimates supplied by experts. See the regulatory
impact analysis for the current rulemaking for more
information regarding these changes, which is
available in the docket.
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and 3-percent discount rate for climate
benefits). For large flares only, we
estimate the monetized benefits are $93
million to $160 million (3-percent
discount rate) and $88 million to $150
million (7-percent discount rate for
health benefits and 3-percent discount
rate for climate benefits). Several
benefits categories, including direct
exposure to SO2 and NOX benefits,
ozone benefits, ecosystem benefits and
visibility benefits are not included in
these monetized benefits. All estimates
are in 2006 dollars for the year 2017.
Although this final rule provides
refiners with some additional
compliance options and removes some
requirements, such as the long-term H2S
limit for flares, the cost savings due this
increased flexibility have not been
calculated for inclusion in the benefitcost analysis.
B. Background of the Refinery NSPS
Section 111(b)(1)(A) of the Clean Air
Act (CAA) requires the EPA to establish
federal standards of performance for
new, modified and reconstructed
sources for source categories which
cause or contribute significantly to air
pollution which may reasonably be
anticipated to endanger public health or
welfare. The standard of performance
must reflect the application of the best
system of emission reductions (BSER)
that (taking into consideration the cost
of achieving such emission reductions,
any non-air quality health and
environmental impact and energy
requirements) the Administrator
determines has been adequately
demonstrated (CAA section 111(a)(1)). If
it is not feasible to prescribe or enforce
a standard of performance, the
Administrator may instead promulgate a
design, equipment, work practice or
operational standard, or a combination
of these types of standards (CAA section
111(h)(1)). Since 1970, the NSPS have
been successful in achieving long-term
emissions reductions in numerous
industries by assuring cost-effective
controls are installed on newly
constructed, reconstructed or modified
sources.
The level of control prescribed by
CAA section 111 historically has been
referred to as ‘‘Best Demonstrated
Technology’’ or BDT. In order to better
reflect that CAA section 111 was
amended in 1990 to clarify that ‘‘best
systems’’ may or may not be
‘‘technology,’’ the EPA is now using the
term ‘‘best system of emission
reduction’’ or BSER in its rulemaking
packages. See, e.g., 76 FR 52738, 52740
(August 23, 2011); 76 FR 63878, 63879
(October 14, 2011). As was done
previously in analyzing BDT, the EPA
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uses available information and
considers the emissions reductions
achieved by the different systems
available and the costs of achieving
those reductions. The EPA also
considers the ‘‘other factors’’ prescribed
by the statute in its BSER analysis. After
considering all of this information, the
EPA then establishes the appropriate
standard representative of BSER.
Sources may use whatever system meets
the standard.
Section 111(b)(1)(B) of the CAA
requires the EPA to periodically review
and, as appropriate, revise the standards
of performance to reflect improvements
in methods for reducing emissions. As
a result of our periodic review of the
NSPS for petroleum refineries (40 CFR
part 60, subpart J), we proposed
amendments to the current standards of
performance and separate standards of
performance for new process units (40
CFR part 60, subpart Ja) (72 FR 27278,
May 14, 2007) and we subsequently
promulgated those amendments and
new standards (73 FR 35838, June 24,
2008). Following promulgation, we
received three separate petitions for
reconsideration from: (1) The American
Petroleum Institute (API), the National
Petrochemical and Refiners Association
(NPRA) and the Western States
Petroleum Association (WSPA)
(collectively referred to as ‘‘Industry
Petitioners’’); (2) HOVENSA, LLC
(‘‘HOVENSA’’); and (3) the
Environmental Integrity Project, Sierra
Club and Natural Resources Defense
Council (collectively referred to as
‘‘Environmental Petitioners’’). On
September 26, 2008, the EPA issued a
Federal Register notice (73 FR 55751)
granting reconsideration of the
following issues: (1) The newly
promulgated flare modification
provision2; (2) the ‘‘flare’’ definition; (3)
the fuel gas combustion device sulfur
limits as they apply to flares; (4) the
flow limit for flares; (5) the total
reduced sulfur and flow monitoring
requirements for flares; and (6) the NOX
limit for process heaters. The EPA also
granted Industry Petitioners’ and
HOVENSA’s request for a 90-day stay
for those same provisions under
reconsideration. On December 22, 2008,
three Federal Register notices (73 FR
78260, 73 FR 78546 and 73 FR 78549)
2 The September 26, 2008, Federal Register notice
(73 FR 55751) described the first issue for which the
EPA granted reconsideration as ‘‘the definition of
‘modification.’’’ However, because what we are
actually reconsidering is the specific flare
modification provision that applies to flares at
petroleum refineries rather than the more generally
applicable definition of ‘‘modification,’’ we have
revised the description of this issue as ‘‘the newly
promulgated flare modification provision.’’
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were published to extend this stay until
a final decision is reached on those
issues.
In the September 26, 2008, Federal
Register notice (73 FR 55751), we also
identified other issues for which
Petitioners requested reconsideration.
We stated that, at that time, we were
‘‘taking no action on all of the other
issues raised in the petitions but will
consider all of the outstanding issues in
a future notice.’’ On December 29, 2009,
we sent a letter to the Petitioners,
through their counsel, stating that ‘‘[t]he
Administrator has decided to grant
reconsideration of all the remaining
issues’’ and that ‘‘EPA will address the
substantive aspects of the issues under
reconsideration through notice and
comment actions published in the
Federal Register.’’ A copy of the letter
to the Petitioners can be found in the
docket for this rulemaking (Docket Item
No. EPA–HQ–OAR–2007–0011–0318).
In this action, we are finalizing the
amendments for which we granted
reconsideration and a stay as outlined in
the September 26, 2008, notice and for
which we proposed amendments on
December 22, 2008. We are also
addressing certain other minor issues
raised by Industry Petitioners in this
action, as discussed later in this
preamble. We will take action on all of
the remaining issues raised by
Petitioners for reconsideration in future
notices.
We received a total of 22 comments
from the following groups on the
proposed amendments during the
public comment period: (1) Refineries,
industry trade associations and
consultants; (2) state and local
environmental and public health
agencies; (3) environmental groups; and
(4) other members of the public. These
final amendments reflect our full
consideration of all of the comments we
received. Detailed responses to the
comments not included in this
preamble, as well as more detailed
summaries of the comments addressed
in this preamble, are contained in
Standards of Performance for Petroleum
Refineries: Background Information for
Final Amendments—Summary of Public
Comments and Responses, dated
December 2011, which is included in
Docket ID No. EPA–HQ–OAR–2007–
0011.
In summary, major comments on the
proposed process heater requirements
were related to the proposed NOX
concentration limits, the alternative
heating value limits, consideration of
turndown (i.e., when a process heater is
operated at less than 50-percent design
capacity) and other factors that
influence the achievable emissions
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limits. In response, we are raising the
limit for new forced draft process
heaters from 40 ppmv NOX at proposal
to 60 ppmv NOX. For both natural draft
and forced draft process heaters, we are
finalizing alternative heating value
limits derived from a more direct
numerical conversion of the NOX
concentration limit (i.e., 0.04 lb/MMBtu
for natural draft and 0.06 lb/MMBtu for
forced draft). For newly constructed,
modified and reconstructed natural
draft and forced draft process heaters,
we are reducing the averaging time for
compliance from a 365-day rolling
average to a 30-day rolling average
applicable during periods of normal
operation. We are also finalizing an
alternative case-specific compliance
option that allows owners and operators
to obtain EPA approval for a sitespecific NOX limit in certain conditions
such as turndown.
Major comments on the proposed
requirements for flares were related to
the definition of flare modification for
purposes of triggering applicability to
this rule, the proposed removal of the
flare flow limit, clarification of flare
monitoring requirements and
clarification of the differences between
the requirement for flares and the
requirements for other fuel gas
combustion devices. We address these
comments by clarifying the definition of
flare modification and by expanding the
list included in the December 22, 2008,
proposal, which specifies certain
connections that do not constitute a
modification of the flare because they
do not result in emissions increases. We
are finalizing the proposed removal of
the flare flow limit and instead, we are
promulgating a suite of work practice
standards that apply to affected flares.
Based on comments received on the
December 22, 2008 proposal, we are
finalizing definitions of ‘‘fuel gas
combustion device’’ and ‘‘flare’’ to
specify that a flare is a separate affected
facility rather than a type of fuel gas
combustion device. We are also
finalizing amendments to clarify certain
monitoring requirements and to provide
additional monitoring alternatives
under certain circumstances.
III. Summary of the Final Rules and
Changes Since Proposal
NSPS for petroleum refineries (40
CFR part 60, subpart J) apply to the
affected facilities at the refinery, such as
fuel gas combustion devices (which
include process heaters, boilers and
flares), that commence construction,
reconstruction or modification after
June 11, 1973, but on or before May 14,
2007 (on or before June 24, 2008 for
flares). The NSPS were originally
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promulgated on March 8, 1974, and
have been amended several times. In
this action, we are promulgating
technical clarifications and corrections
to subpart J.
New standards of performance for
petroleum refineries (40 CFR part 60,
subpart Ja) apply to flares that
commence construction, reconstruction
or modification after June 24, 2008, and
other affected facilities at petroleum
refineries, including process heaters and
other fuel gas combustion devices that
commence construction, reconstruction
or modification after May 14, 2007. In
this action, we are finalizing
amendments to subpart Ja to address the
issues raised by Petitioners regarding
flares and process heaters. We are also
finalizing technical corrections to
subpart Ja for certain issues that were
identified by Industry Petitioners in
their August 21, 2008, supplement to
their original administrative
reconsideration request (Docket Item
No. EPA–HQ–OAR–2007–0011–0246).
The following sections summarize the
amendments in both 40 CFR part 60,
subpart J and 40 CFR part 60, subpart Ja.
Section IV contains the rationale for
these amendments, while the
amendments themselves follow the
preamble.
A. What are the final amendments to
the standards of performance for
petroleum refineries (40 CFR part 60,
subpart J)?
The final amendments add a new
paragraph to 40 CFR 60.100 to allow 40
CFR part 60, subpart J affected sources
the option of complying with subpart J
by following the requirements in 40 CFR
part 60, subpart Ja. The subpart Ja
requirements are at least as stringent as
those in subpart J, so providing this
option will allow all process units in a
refinery to follow the same requirements
and simplify compliance. We are also
removing the reference to 40 CFR
60.101a from the description of the
applicability dates in 40 CFR 60.100(b)
so as not to cause confusion over the
definition of ‘‘flare’’ in subpart J. We are
finalizing a correction to the value and
units (in the metric system) for the
allowable incremental rate of particulate
matter (PM) emissions in 40 CFR
60.106(c)(1). We amended the units for
this constant in 40 CFR 60.102(b) on
June 24, 2008, and we are now
correcting 40 CFR 60.106(c)(1)
accordingly. Finally, we are finalizing a
definition of ‘‘fuel gas’’ that incorporates
the same clarifications regarding vapors
from wastewater treatment units and
marine tank vessel loading operations
identified in the subpart Ja definition of
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56427
‘‘fuel gas’’ (described later in this
preamble).
B. What are the final amendments to the
standards of performance for process
heaters (40 CFR part 60, subpart Ja)?
We proposed several amendments to
the standards of performance for process
heaters, including adding emission
limits in units of lb/MMBtu, extending
the emission limit averaging time from
24 hours to 365 days, raising the
emission limit for modified and
reconstructed forced draft process
heaters and raising the emission limit
for co-fired process heaters. After
consideration of all of the public
comments and our own additional
analyses, we are finalizing the process
heater requirements, as described in this
section.
Table 3 presents a comparison of the
proposed and final 40 CFR part 60,
subpart Ja amendments for process
heaters. The final amendments include
four subcategories of process heaters: (1)
Natural draft process heaters; (2) forced
draft process heaters; (3) co-fired natural
draft process heaters; and (4) co-fired
forced draft process heaters. At
proposal, all co-fired process heaters
were included in one subcategory, for a
total of three process heater
subcategories, but, based on emissions
data from co-fired process heaters, we
divided natural draft and forced draft
co-fired process heaters into separate
subcategories with different emissions
limits.
For each of the first two subcategories,
the final amendments include a
concentration-based NOX emissions
limit and a heating value-based NOX
emissions limit, both determined daily
on a 30-day rolling average basis. For
the natural draft process heater
subcategory, the concentration-based
NOX emissions limit for newly
constructed, modified and reconstructed
natural draft process heaters is 40 ppmv
(dry basis, corrected to 0-percent excess
air) determined daily on a 30-day rolling
average basis. The heating value-based
NOX emissions limit for newly
constructed, modified and reconstructed
natural draft process heaters is 0.040 lb/
MMBtu higher heating value basis
determined daily on a 30-day rolling
average basis. The averaging time for
both of these limits is shorter than the
365-day averaging time that was
proposed, and the heating value-based
NOX emissions limit differs from the
proposed limit in that it is a more direct
numerical conversion from 40 ppmv
NOX. At proposal, we provided a longer
averaging time so that short periods of
turndown (i.e., when a process heater is
operating at less than 50-percent design
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capacity) would not significantly affect
the overall performance of the unit. Our
analysis of the additional data that we
obtained following the proposal
supported revising all NOX emissions
limits to be on a 30-day rolling average
basis, which is achievable for process
heaters during periods of normal
operation. These data indicate that
process heaters equipped with ultra low
NOX burners meet the emission limits
described above if compliance is
determined on a 30-day rolling average
basis. We are finalizing alternative
compliance options that allow the
owners and operator to establish sitespecific limits applicable during certain
conditions such as turndown. Section
IV.A of this preamble provides
additional information regarding the
rationale and analyses leading to these
final amendments.
For the second subcategory, forced
draft process heaters, the concentrationbased NOX emissions limit for newly
constructed, modified and reconstructed
forced draft process heaters is 60 ppmv
(dry basis, corrected to 0-percent excess
air) determined daily on a 30-day rolling
average basis. The heating value-based
NOX emissions limit for newly
constructed, modified and reconstructed
forced draft process heaters is 0.060 lb/
MMBtu higher heating value basis
determined daily on a 30-day rolling
average basis. The higher limit for new
forced draft process heaters (at proposal,
the limit was 40 ppmv) is based on
additional data and a re-evaluation of
BSER, as described later in this
preamble. As with natural draft process
heaters, the averaging time for both of
these limits is shorter than proposed,
and the final heating value-based NOX
emissions limit is a more direct
numerical conversion from 60 ppmv
NOX. Section IV.A of this preamble
provides additional information
regarding the rationale and analyses
leading to these final amendments.
For each of these subcategories, a
process heater need only meet either the
concentration-based NOX emissions
limit or the heating value-based NOX
emissions limit. The refinery owner or
operator may choose to comply with
either limit at any time, provided that
they are monitoring the appropriate
variables to assess the heating valuebased NOX emissions limit. If the
refinery owner or operator does not
choose to monitor fuel composition,
then they must comply with the
concentration-based NOX emissions
limit.
TABLE 3—PROPOSED AND FINAL AMENDMENTS FOR PROCESS HEATERS
Proposal
(December 22, 2008)
Averaging time ...................................................
Natural Draft NOX Emission Limits ....................
Forced Draft NOX Emission Limits ....................
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Co-fired Burner (oil and gas) NOX Emission
Limits.
As proposed, initial compliance with
the heating value-based emissions limits
will be demonstrated by conducting a
performance evaluation of the
continuous emission monitoring system
(CEMS) in accordance with Performance
Specification 2 in appendix B to 40 CFR
part 60, with EPA Method 7 of 40 CFR
part 60, appendix A–4 as the Reference
Method, along with fuel flow
measurements and fuel gas
compositional analysis. The NOX
emission rate is calculated using the
oxygen (O2)-based F factor, dry basis
according to EPA Method 19 of 40 CFR
part 60, appendix A–7. Ongoing
compliance with this NOX emissions
limit is determined using a NOX CEMS
and at least daily sampling of fuel gas
heat content or composition to calculate
a daily average heating value-based
emissions rate, which is subsequently
used to determine the 30-day average.
The third and fourth subcategories of
process heaters are co-fired process
heaters. A co-fired process heater is a
process heater that employs burners that
are designed to be supplied by both
gaseous and liquid fuels. As described
in more detail in section IV.A of this
preamble, co-fired process heaters do
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Final
365-day rolling average ...................................
40 ppmv or 0.035 lb/MM BTU .........................
New: 40 ppmv or 0.035 lb/MM BTU ................
M/R: 60 ppmv or 0.055 lb/MM BTU
150 ppmv or Weighted average based on oil
at 0.27 lb/MM BTU and gas at 0.08 lb/MM
BTU.
not include gas-fired process heaters
that have emergency oil back-up
burners. There are two compliance
options for each subcategory of co-fired
process heaters: (1) 150 ppmv (dry basis,
corrected to 0-percent excess air)
determined daily on a 30 successive
operating day rolling average basis; and
(2) a source-specific daily average
emissions limit. Unlike gas-fired process
heaters, the owner or operator of a cofired process heater must choose one
emissions limit and show compliance
with that limit. For co-fired natural draft
process heaters, the daily average
emissions limit is based on a limit of
0.06 lb/MMBtu for the gas portion of the
firing and 0.35 lb/MMBtu for the oil
portion of the firing. For co-fired forced
draft process heaters, the daily average
emissions limit is based on a limit of
0.11 lb/MMBtu for the gas portion of the
firing and 0.40 lb/MMBtu for the oil
portion of the firing. These limits are
different than proposed, based on a reevaluation of BSER with new data
received during the public comment
period. All of the requirements for
emissions monitoring, recordkeeping
and reporting for co-fired process
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30-day rolling average.
40 ppmv or 0.04 lb/MM BTU.
60 ppmv or 0.06 lb/MM BTU.
150 ppmv or Weighted average based on oil
at 0.40 lb/MM BTU and gas at 0.11 lb/MM
BTU forced draft and weighted average
based on oil at 0.35 lb/MM BTU and gas at
0.06 lb/MM BTU for natural draft.
heaters are the same as for the other
process heater subcategories.
We are also finalizing an alternative
compliance option that allows owners
and operators to obtain EPA approval
for a site-specific NOX limit for certain
process heaters. This compliance option
was provided in the proposed
amendments, but it was limited to (1)
natural draft and forced draft modified
or reconstructed process heaters that
lack sufficient space to accommodate
combustion modification-based
technology and (2) natural draft and
forced draft co-fired process heaters. In
the final amendments, we are finalizing
this compliance option for those process
heaters mentioned above while also
providing this compliance option for the
following additional types of process
heaters: (3) modified or reconstructed
induced draft process heaters that have
downwardly firing burners and (4)
forced draft and natural draft process
heaters that operate at low firing rates,
or turndown, for an extended period of
time. As we noted in the preamble to
the proposed amendments, in limited
cases, existing natural draft or forced
draft process heaters have limited
firebox size or other constraints such
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that they cannot apply the BSER of
ultra-low NOX burners or otherwise
meet the applicable limit and some cofired units may not be able to achieve
the NOX limitations even with ultra-low
NOX burner control technology. In
addition, commenters noted that
downwardly fired process heaters with
induced draft fans have similar NOX
control issues as forced draft heaters,
but the definition of forced draft heater
does not include these induced draft
heaters (these are defined as natural
draft process heaters). Therefore, we
added a provision to allow induced
draft process heaters with downwardlyfiring burners to use the alternative
compliance option.
Finally, we note that the emissions
limits for forced draft and natural draft
gas-fired process heaters are based on
the performance of ultra-low NOX
burner control technologies. The ultralow NOX burner technology suppliers
recommend operating with higher
excess air rates at low firing rates (at or
below approximately one-half of the
maximum firing capacity), which causes
higher NOX concentrations at low firing
rates. Therefore, all types of process
heaters with ultra-low NOX burner
control technologies may be unable to
meet the emissions limits if they are
operated at low firing rates for an
extended period of time. Requesting a
site-specific emissions limit requires a
detailed demonstration that the
application of the ultra-low NOX burner
technology is not feasible or that the
technology cannot meet the NOX
emissions limits given the conditions of
the process heater (downward fired
induced draft, co-fired or prolonged
turndown); the refinery must also
conduct source tests in developing a
site-specific emissions limit for its
process heater. This analysis must be
submitted to and approved by the
Administrator.
We are finalizing the proposed
clarification that owners and operators
of process heaters in any subcategory
with a rated heating capacity of less
than 100 million British thermal units
per hour (MMBtu/hr) have the option of
using CEMS. The final rule states that
owners and operators of process heaters
subject to 40 CFR part 60, subpart Ja
should use CEMS to demonstrate
compliance unless the heater is
equipped with combustion
modification-based technology (lowNOX burners or ultra-low NOX burners)
with a rated heating capacity of less
than 100 MMBtu/hr; owners and
operators of those specific process
heaters have the alternative option of
biennial source testing to determine
compliance. As requested by
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commenters, we have provided
additional detail in the final rule
regarding how to develop the O2
operating limit, including provisions on
how to develop an O2 operating curve
to ensure compliance with the NOX
emission limit at different process
heater firing rates. We are requiring that
owners and operators with process
heaters in any subcategory that are
complying using biennial source testing
establish a maximum excess O2
concentration operating limit or
operating curve that can be met at all
times, even during turndown, and
comply with the O2 monitoring
requirements for ongoing compliance
demonstration.
C. What are the final amendments to the
standards of performance for flares (40
CFR part 60, subpart Ja)?
We proposed several amendments to
the standards of performance for flares,
including, but not limited to, amending
the flare modification provision,
removing the numerical limit on the
flow rate to the flare, revising the flare
management plan requirements to
include a list of connections to the flare
and an identification of baseline
conditions, clarifying when a root cause
analysis is required, revising the sulfur
and flow monitoring requirements and
providing additional time for
compliance. After consideration of all of
the public comments, and our own
additional analyses, we are finalizing
the flare requirements, as described in
this section.
We did not propose to revise the
definitions of ‘‘fuel gas combustion
device’’ and ‘‘flare’’ on December 22,
2008. However, based on public
comment and changes to the flare
requirements, as described later in this
section, we have decided to finalize
revisions to these definitions to specify
that, for purposes of 40 CFR part 60,
subpart Ja, a flare is a separate affected
facility rather than a type of fuel gas
combustion device. This change makes
clearer the differences between the
requirements for flares and the
requirements for fuel gas combustion
devices, particularly in terms of sulfur
and flow rate monitoring requirements
and thresholds for root cause analyses
and corrective action analyses. We are
also making corrections, as needed, in
numerous paragraphs throughout
subpart Ja for consistency with the
amended definitions (e.g., adding ‘‘and
flares,’’ where applicable, to paragraphs
with requirements for ‘‘fuel gas
combustion devices’’).
We are finalizing the flare
modification provision in 40 CFR
60.100a(c), as described below, to
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56429
specify certain connections to a flare
that do not constitute a modification of
the flare because they do not result in
emissions increases. On December 22,
2008, we proposed that the following
types of connections to a flare would
not be considered a modification of the
flare: (1) Connections made to install
monitoring systems to the flares; (2)
connections made to install a flare gas
recovery system; (3) connections made
to replace or upgrade existing pressure
relief or safety valves, provided the new
pressure relief or safety valve has a set
point opening pressure no lower and an
internal diameter no greater than the
existing equipment being replaced or
upgraded; and (4) replacing piping or
moving an existing connection from a
refinery process unit to a new location
in the same flare, provided the new pipe
diameter is less than or equal to the
diameter of the pipe/connection being
replaced/moved. We are finalizing those
proposed amendments and also adding
the following types of connections to
the list of connections to flares that are
not modifications of flares: (1)
Connections between flares; (2)
connections for flare gas sulfur removal;
and (3) connections made to install
redundant flare equipment (such as a
back-up compressor). We are also
clarifying one of the proposed
exemptions to indicate that connections
made to upgrade or enhance
components of flare gas recovery
systems (e.g., additional compressors or
recycle lines) are not modifications.
We are not finalizing the proposed
amendment to provide additional time
for flares that need to install additional
amine scrubbing and amine stripping
columns to meet the requirement to
limit the long-term concentration of H2S
to 60 ppmv (determined daily on a 365
successive calendar day rolling average
basis) (hereafter referred to as the longterm 60 ppmv H2S fuel gas
concentration limit). Instead, based on
comments received during the public
comment period for the proposed
amendments and our own additional
analyses, we are removing the
requirement for flares to meet the longterm 60 ppmv H2S fuel gas
concentration limit. As explained in
section IV, we determined that requiring
refineries to ensure the fuel gas they
send to their flares meets a long-term
H2S concentration of 60 ppmv is not
appropriate for flares.
We are promulgating final
amendments for flares that include a
suite of standards that apply at all times
that are aimed at reducing SO2
emissions from flares. These
amendments include several provisions
that were proposed on December 22,
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2008, as well as others that differ from
those proposed, but are a logical
outgrowth of the proposed amendments.
This suite of standards requires
refineries to: (1) Develop and implement
a flare management plan; (2) conduct
root cause analyses and take corrective
action when waste gas sent to the flare
exceeds a flow rate of 500,000 standard
cubic feet (scf) above the baseline flow
to a flare in any 24-hour period (rather
than the proposed threshold of 500,000
scf in any 24-hour period without
considering the baseline); (3) conduct
root cause analyses and take corrective
action when the emissions from the
flare exceed 500 lb of SO2 in a 24-hour
period (instead of 500 lb SO2 above the
emissions limit); and (4) optimize
management of the fuel gas by limiting
the short-term concentration of H2S to
162 ppmv during normal operating
conditions (determined hourly on a 3hour rolling average basis). As
explained further in preamble section
IV.B, 40 CFR part 60, subpart J sets a
performance standard for SO2
(expressed as a 162 ppmv short-term
H2S concentration limit) in fuel gas
entering fuel gas combustion devices.
However, for this final rule, we have
determined that flares should be treated
separately from other fuel gas
combustion devices because they meet
the criteria set forth in CAA section
111(h)(2)(A) since emissions from a flare
do not occur ‘‘through a conveyance
designed and constructed to emit or
capture such pollutant.’’ The flare itself
is not a ‘‘conveyance’’ that is ’’emitting’’
or ‘‘capturing’’ these pollutants. Instead,
pollutants such as SO2 are created in the
flame that burns outside the flare tip.
Therefore, we have determined that this
suite of work practice standards, which
includes optimization of fuel gas
management (based on limiting
concentration of H2S to 160 ppmv) is
more appropriate for flares, as opposed
to the H2S performance standard in
subpart J, applicable to fuel gas systems.
See section IV.B of this preamble for a
more detailed explanation of these
requirements. In this rule, we are using
the term ‘‘normal operating conditions’’
to describe situations where the process
is operating in a routine, predictable
manner, such that the gases from the
process are predictable, as opposed to
less-predictable swings related to
emergency situations during which the
flare begins to operate as a safety device.
All of these requirements will apply
during the vast majority of the time.
Under a very narrow and limited set of
circumstances, such as when a flare is
used as a safety device under emergency
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conditions,3 the flare will be subject to
all of these requirements except for the
requirement to optimize management of
the fuel gas.
In addition, we are specifying that, if
a discharge exceeding either or both of
the SO2 or flow thresholds described
above is the result of a planned startup
or shutdown of a refinery process unit
or ancillary equipment connected to the
flare, and the flare management plan
procedures for minimizing flow (which
minimizes emissions) during that type
of event are followed, a root cause
analysis and corrective action analysis
are not required. Finally, we are
finalizing the proposed added
provisions to ensure that owners and
operators implement corrective actions
on the findings of the SO2 or flow rate
root cause analyses and to specify a
deadline for performing the corrective
actions.
We are finalizing the proposed
amendment to remove the 250,000 scfd
30-day average flow rate limit. Our
rationale for this decision is explained
in the preamble to the proposed
amendments (73 FR 78530) and also in
section IV of this preamble.
We are finalizing one proposed
amendment to the flare management
plan and adding several new
requirements as a logical outgrowth of
the proposed amendments, considering
the public comments we received, to
ensure compliance with the flare
standards. First, as proposed, we are
requiring a list of refinery process units
and fuel gas systems connected to each
affected flare. However, we are also
adding a requirement for a simple
process flow diagram showing the
design of the flare, connections to the
flare header and subheader system(s),
and all gas lines associated with the
flare. With these two requirements, we
are clarifying that the flare management
plan must include a diagram of the flare
and connections, but the diagram need
not be a detailed piping and
instrumentation diagram that shows all
process units and ancillary equipment
connected to the flare. We are also
requiring the owner and operator of an
affected flare to assess and minimize
flow to affected flares from these
process units and fuel gas systems.
Second, we are adding new
requirements that the flare management
plan include design and operation
details about the affected flare,
including tip diameter, type of flare,
monitoring methods and a description
3 Background Information for New Source
Performance Standards, Vol. 3, Promulgated
Standards (APTD–1352c; Publication No. EPA 450/
2–74–003), pg 127 (February 1974) (NSPS BID Vol.
3).
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of the flare gas recovery system, if
present. The inclusion of these details
will ensure that the rest of the flare
management plan is reasonable and
appropriate for that affected flare.
Third, as a logical outgrowth of the
proposed amendments, considering the
public comments we received, we are
adding a new requirement for owners
and operators to determine the baseline
flow to each flare, including purge and
sweep gas, and include this baseline
flow in the flare management plan. As
described later in this preamble,
developing the baseline is important
because the final threshold for the flare
flow root cause analysis takes this
baseline flow into consideration.
Finally, we are adding a new
requirement to minimize the volume of
gas flared during maintenance of a flare
gas recovery system.
We have decided to remove the
requirement for the owner or operator to
explain in the flare management plan
how a root cause analysis and corrective
action analysis will be conducted if the
flow to the flare exceeds the specified
threshold. Instead, all the requirements
for determining when and how to
conduct a root cause analysis and
corrective action analysis, and the
requirements for when and how to
implement a corrective action, have
been expanded, as described later in
this section, and moved to 40 CFR
60.103a(c) through (e).
We are specifying that, for modified
flares, the flare management plan must
be developed and implemented by no
later than November 11, 2015 or upon
startup of the modified flare, whichever
is later (the proposed amendments
provided 18 months with an additional
6 months if the owner or operator
committed to installing a flare gas
recovery system). In addition, because
of the lack of a direct flow limit and the
addition of the baseline flow value, we
are adding a requirement that the flare
management plan must be submitted to
the Administrator.
As with the flare management plan,
the owner or operator of an affected
flare must comply with the root cause
analysis and corrective action analysis
requirements within 3 years from the
effective date of this final rule or upon
startup of the modified flare, whichever
is later.
We are finalizing several proposed
amendments to the sulfur monitoring
requirements and revising other
requirements as a logical outgrowth of
the proposed amendments, considering
the public comments we received. We
consolidated the proposed alternatives
to monitor reduced sulfur compounds
and total sulfur compounds into a
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provision that allows the use of total
reduced sulfur monitoring. We also
clarified the span requirements for these
monitors and are allowing the use of
cylinder gas audits for relative accuracy
assessments. We are finalizing the H2S
monitoring alternative method for
determining total sulfur content in the
flare gas, as proposed, but we have
clarified the span requirements for this
monitor and are allowing the use of
cylinder gas audits for relative accuracy
assessments, similar to the total reduced
sulfur monitor requirements. For
refineries that measure SO2
concentrations in the exhaust from a
fuel gas combustion device that
combusts gas representative of the gas
discharged to the flare, we added an
alternative to allow the owner or
operator to use the existing SO2 CEMS
data to calculate the total sulfur content
in the flare gas.
We received public comments stating
that the flow and sulfur monitoring
requirements for flares were too
burdensome for flares that are used
infrequently or that are configured such
that they cannot receive high sulfur flare
gas. Based on our evaluation of these
comments, we are providing new
alternatives to continuous flow and
sulfur monitoring for certain flares.
First, for flares that are configured such
that they only receive inherently low
sulfur gas streams described in 40 CFR
60.107a(a)(3)(i) through (iv) or (b),
continuous sulfur monitors are not
necessary because a root cause analysis
will be triggered by an exceedance of
the flow rate threshold long before they
exceed the 500 lb SO2 trigger in a 24hour period.
Second, we are providing an
alternative monitoring option for
emergency flares, secondary flares and
flares equipped with a flare gas recovery
system designed, sized and operated to
capture all flows (except flows resulting
from planned startup and shutdown that
are addressed in the flare management
plan). If this option is applicable, the
owner or operator may elect to
continuously monitor the water seal
height and the pressure in the flare
header just upstream of the water seal
rather than install total sulfur and flow
monitoring systems. If this monitoring
option is selected, any instance where
the pressure upstream of the water seal
(expressed in inches of water) exceeds
the water seal height triggers a
requirement to perform a root cause
analysis and corrective action analysis,
unless the discharge is related to flare
gas recovery system compressor cycling
or a planned startup or shutdown (of a
refinery process unit or ancillary
equipment connected to the flare)
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following the procedures in the flare
management plan. An ‘‘emergency
flare’’ is a flare that combusts gas
exclusively released as a result of
malfunctions (and not startup,
shutdown, routine operations or any
other cause) and is characterized as
having four or fewer discharge events in
any 365 consecutive calendar days.
Owners or operators of affected flares
that have flare gas recovery systems
with staged compressors that elect to
use this monitoring option must identify
these flares in their flare management
plan, identify the time period required
for the staged compressors to actively
start to recover gas and identify the
operating parameters monitored and
procedures employed to minimize the
duration of flaring during compressor
staging. If a pressure exceedance is
caused during compressor staging and
the duration of the pressure exceedance
is less than the time specified in the
flare management plan, then a root
cause analysis is not required and the
pressure exceedance is not required to
be reported. If a pressure exceedance is
not attributable to compressor staging
(i.e., all staged compressors are active),
if a pressure exceedance is the result of
a planned startup and shutdown event
during which the flare management
plan is not followed or if the duration
of a pressure exceedance attributable to
compressor staging is greater than the
time specified in the flare management
plan, then a root cause analysis and
corrective action analysis are required
and the pressure exceedance must be
reported. More than four pressure
exceedances required to be reported, as
described above and under 40 CFR
60.108a(d)(5) (hereafter referred to as
‘‘reportable pressure exceedances’’) in
any 365 consecutive calendar days is an
indication that the flare gas recovery
system is not adequately sized, and the
sulfur and flow monitors, as required in
40 CFR 60.107a(e) and (f), must be
installed if that occurs.
Third, we are clarifying that monitors
for flow and sulfur on the second flare
in a staged flare configuration are not
required where the water seal
monitoring requirements adequately
and appropriately address this scenario.
Under most circumstances, the root
cause analysis is expected to be
triggered, based on the flow to or
emissions from the primary flare.
However, in cases where the capacity of
the primary flare is small (less than
500,000 scfd), this may not always be
the case. Additionally, we consider the
water seal monitoring on the secondary
flare to be appropriate to ensure that
gases are not released to the secondary
flare inadvertently. We clarify in this
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56431
final rule that if a root cause analysis is
triggered for the primary flare, releases
to the secondary flare do not trigger an
additional root cause analysis (i.e., the
releases may be treated as one event).
However, if flow is diverted to the
secondary flare, then a root cause
analysis is required, even if a root cause
analysis was not triggered for the
primary flare, based on flow rate or SO2
emissions. In addition, if flow is
diverted to the secondary flare five or
more times in a 365-day period, flow
monitoring of the secondary flare is
required. We anticipate that the
upstream sulfur monitor on the primary
flare can be used to determine the sulfur
content of the gas diverted to the
secondary flare.
In response to comments, we are also
finalizing a new amendment providing
an alternative compliance option in 40
CFR 60.103a(g) and 40 CFR 60.107a(h)
for certain flares. Specifically, for
refineries located in the SCAQMD, an
affected flare subject to 40 CFR part 60,
subpart Ja may elect to comply with
SCAQMD Rule 1118 as an alternative to
complying with the requirements for
flares in 40 CFR 60.103a(a) through (e)
and the associated monitoring
provisions in 40 CFR 60.107a(e) and (f).
Similarly, for refineries located in the
BAAQMD, an affected flare subject to
subpart Ja may elect to comply with
both BAAQMD Regulation 12, Rule 11
and BAAQMD Regulation 12, Rule 12 as
an alternative to complying with the
requirements for flares in 40 CFR
60.103a(a) through (e) and the
associated monitoring provisions in 40
CFR 60.107a(e) and (f). We are also
finalizing specific provisions within the
standards for owners or operators (and
manufacturers of equipment) to submit
a request for a determination of
equivalence for ‘‘an alternative means of
emission limitation’’ that will achieve a
reduction in emissions at least
equivalent to the reduction in emissions
achieved under any of the final subpart
Ja design, equipment, work practice or
operational requirements in accordance
with CAA section 111(h).
For fuel gas combustion devices and
sulfur recovery plants, we are correcting
and clarifying the threshold for a root
cause analysis and corrective action
analysis. The proposed root cause
analysis threshold for both types of
process units was 500 lb SO2 above the
emission limit, but the proposed
amendments directed the owner or
operator to compare the SO2 emissions
to ‘‘the period of the exceedance’’ for
fuel gas combustion devices and ‘‘the
entire 24-hour period’’ for sulfur
recovery plants. That language meant
that if one 12-hour average for a sulfur
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recovery plant was above the emission
limit, the owner or operator would have
compared those emissions to the
emissions allowed over an entire 24
hours to determine if root cause analysis
was required. However, although a 12hour average above the emission limit
clearly means that more SO2 was
emitted than allowed by that emissions
limit, it is possible that, since the time
periods being compared were not
analogous, the ‘‘allowed emissions’’
over 24 hours could be more than the
actual emissions that made up the one
12-hour average. Upon further
consideration, we see no reason for the
requirements to be different for fuel gas
combustion devices and sulfur recovery
plants. Therefore, we are finalizing an
amendment that states that the
threshold for a root cause analysis and
corrective action analysis for both sulfur
recovery plants and fuel gas combustion
devices is 500 lb above the emission
limit during one or more consecutive
periods of excess emissions 4 or any 24hour period, whichever is shorter. This
clarifying amendment is needed to
ensure that the magnitude of the
emissions limit exceedance is properly
compared to what would have been
emitted if the emissions were equivalent
to the emissions limit based on the
averaging time allowed for that
emissions limit.
Finally, we are finalizing the
amendments at 40 CFR 60.108a(c) and
(d) mostly as proposed to clarify
recordkeeping and reporting when a
root cause analysis and corrective action
analysis are required. These
clarifications were needed to more
clearly delineate the differences in the
recordkeeping and reporting
requirements for flares, fuel gas
combustion devices and sulfur recovery
plants. The differences between the
proposed amendments and the final
amendments are corrections to be
consistent with changes to the root
cause analysis and corrective action
analysis requirements already
described. We are also finalizing 40 CFR
60.108a(c), as proposed, to add
recordkeeping requirements for the
proposed monitoring option that is
based on periodic manual sampling and
analysis to determine the total sulfur-toH2S ratio.
4 As noted above, the proposed amendments used
the term ‘‘period of the exceedance’’ for fuel gas
combustion devices. That term was intended to
have the same meaning as a period of excess
emissions (or multiple consecutive periods of
excess emissions), as defined in 40 CFR 60.106a(b)
or 40 CFR 60.107a(i)). Therefore, the final
amendments refer to ‘‘one or more consecutive
periods of excess emissions’’ rather than ‘‘period of
the exceedance.’’
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D. What are the final amendments to the
definitions in 40 CFR part 60, subpart
Ja?
We proposed amendments to a
number of definitions in 40 CFR
60.101a. This section describes whether
we are finalizing the amendments as
proposed, finalizing an amendment
different than (but as a logical
outgrowth of) what was proposed or not
finalizing the proposed amendment.
We are finalizing amendments to the
definitions of ‘‘flexicoking unit’’ and
‘‘fluid coking unit,’’ as proposed.
We are finalizing a definition of
‘‘delayed coking unit’’ that is different
than the proposed amendments to
clarify what pieces are included in a
delayed coking unit. The final June 2008
rule did not explicitly describe the
pieces of a delayed coking unit. We
proposed to amend the definition in
December 2008 to specify that a delayed
coking unit ‘‘consists of the coke drums
and associated fractionator.’’ In the
course of evaluating public comments
on the proposed definition, we looked
more closely at the operation of delayed
coking units and determined that the
fractionators, quench water system and
coke cutting equipment are integral to
the operation of a delayed coking unit.
Therefore, we are revising the definition
of ‘‘delayed coking unit’’ in these final
amendments to include ‘‘the coke
drums associated with a single
fractionator and the associated
fractionator; the coke drum cutting
water and quench system, including the
jet pump and coker quench water tank;
process piping and associated
equipment such as pumps, valves and
connectors; and the coke drum
blowdown recovery compressor
system.’’ Finally, to avoid any potential
retroactive compliance issues that could
arise for certain delayed coking units
because of the changes to the definition
of ‘‘delayed coking unit’’ between the
proposal and the final rule, we are
moving the date for determining
applicability of NSPS subpart Ja for
those newly constructed, reconstructed
and modified delayed coking units
specifically affected by this change from
the date of the proposal to the
promulgation date of these final
amendments. See CAA section
111(a)(2).
We are finalizing definitions of
‘‘forced draft process heater,’’ ‘‘natural
draft process heater’’ and ‘‘co-fired
process heater,’’ which will enable
owners and operators to determine the
appropriate subcategory for each of their
process heaters. Based on public
comments, the final amendments have
been revised slightly from the proposed
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definitions to clarify that induced draft
systems are defined as natural draft
process heaters and balanced draft
systems are defined as forced draft
process heaters. We are also revising the
definition of ‘‘co-fired process heater’’ to
clarify that this type of process heater
does not include gas burners that have
emergency oil back-up burners. We are
finalizing the definition of ‘‘air
preheat,’’ as proposed, except that we
are substituting the term ‘‘sensible’’ for
‘‘latent’’ to describe the heat recovered
from exhaust gases.
We are finalizing the definitions of
‘‘flare gas recovery system’’ and
‘‘process upset gas,’’ as proposed, and
we are adding a new definition of ‘‘flare
gas header system.’’ We are finalizing a
revision to the definition of ‘‘flare’’ to
refer to the ‘‘flare gas header system’’
rather than repeat the components of the
flare gas header system within the
definition of flare. In addition, we are
clarifying in the definition of ‘‘flare’’
that, in the case of an interconnected
flare gas header system (i.e., two or more
flare tips share the same flare gas header
system or are otherwise connected such
that they receive flare gas from the same
source), the ‘‘flare’’ includes each
combustion device serviced by the
interconnected flare gas header system
and the interconnected flare gas header
system.
We are finalizing definitions of
‘‘corrective action,’’ ‘‘corrective action
analysis’’ and ‘‘root cause analysis’’
with minor changes from proposal to
update section references and to expand
upon the types of factors that should be
taken into consideration for root cause
and corrective action analyses. We are
adding definitions of ‘‘purge gas’’ and
‘‘sweep gas’’ to clarify the requirements
of the flare minimization plan. We are
also adding new definitions of
‘‘emergency flare,’’ ‘‘cascaded flare
system,’’ ‘‘non-emergency flare,’’
‘‘primary flare’’ and ‘‘secondary flare’’ to
clarify the types of flares that are and
are not allowed to use the water seal
monitoring alternative for flares.
We are finalizing the amendments to
the definition of ‘‘petroleum refinery,’’
as proposed. As we noted in the
preamble to the proposed amendments,
facilities that only produce oil shale or
tar sands-derived crude oil for further
processing using only solvent extraction
and/or distillation to recover diluent
that is then sent to a petroleum refinery
are not themselves petroleum refineries.
Facilities that produce oil shale or tar
sands-derived crude oil and then
upgrade these materials and produce
refined products would be petroleum
refineries. Additionally, facilities that
produce oil shale or tar sands-derived
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crude oil using any cracking process
would be considered petroleum
refineries.
We are not finalizing the proposed
amendments to ‘‘refinery process unit’’
to avoid possible conflicts and
confusion caused by having different
definitions for ‘‘refinery process unit’’ in
40 CFR part 60, subparts J and Ja, but
we are adding a new definition of
‘‘ancillary equipment’’ and using this
term to clarify that the flare
modification provisions and standards
apply to the types of units listed in the
proposed definition of ‘‘refinery process
unit.’’ Specifically, we are defining
ancillary equipment as equipment used
in conjunction with or that serve a
refinery process unit. Ancillary
equipment includes, but is not limited
to, storage tanks, product loading
operations, wastewater treatment
systems, steam- or electricity-producing
units (including coke gasification units),
pressure relief valves, pumps, sampling
vents and continuous analyzer vents.
We are amending the definition of
‘‘fuel gas,’’ as proposed, to clarify that
process units that gasify petroleum coke
at a petroleum refinery are producing
refinery fuel gases. We also proposed to
amend the definition to state that gas
generated by process units that calcine
petroleum coke into anode grade coke is
not fuel gas. Based on public comment,
we are amending the definition to state
that gas generated by coke calciners
producing all premium grade coke
(rather than just anode grade coke, as
proposed) is not fuel gas. Also upon
consideration of public comments, we
are amending the definition of ‘‘fuel
gas’’ to clarify which vapor streams we
intended to exclude. The proposed
definition indicated that vapors
collected and combusted to comply
with specific standards were not
considered fuel gas. The final amended
definition clarifies that vapors that are
collected and combusted in a thermal
oxidizer or flare installed to control
emissions from wastewater treatment
units other than those processing sour
water, marine tank vessel loading
operations and asphalt processing units
are not considered fuel gas, regardless of
whether the action is required by
another standard.
Finally, we are finalizing several
proposed amendments to the definition
of ‘‘sulfur recovery plant’’ to clarify the
intent of the definition. We are
56433
correcting the spelling of ‘‘H2S.’’ We are
also clarifying that multiple units
recovering sulfur from a common source
of sour gas produced at a refinery are
considered one sulfur recovery plant. In
addition, we are clarifying that loading
facilities downstream of the sulfur pits
are not part of the sulfur recovery plant
(the proposed definition only specified
secondary sulfur storage vessels).
E. What are the final technical
corrections to 40 CFR part 60, subpart
Ja?
See Table 4 of this preamble for
miscellaneous technical corrections that
we are finalizing throughout 40 CFR
part 60, subpart Ja. As mentioned
previously, some of these technical
corrections are in response to
straightforward issues raised by
Industry Petitioners in their August 21,
2008, supplement to their original
petition for reconsideration (Docket
Item No. EPA–HQ–OAR–2007–0011–
0246). Other technical corrections are
needed to correct typographical errors
and to correct equation and paragraph
designations.
TABLE 4—TECHNICAL CORRECTIONS TO 40 CFR PART 60, SUBPART JA
Section
Technical correction and reason
60.102a(f)(1)(ii) ............................
Replace ‘‘300 ppm by volume of reduced sulfur compounds and 10 ppm by volume of hydrogen sulfide
(HS2), each calculated as ppm SO2 by volume (dry basis) at zero percent excess air’’ with ‘‘300 ppmv of
reduced sulfur compounds and 10 ppmv of H2S, each calculated as ppmv SO2 (dry basis) at 0-percent excess air’’ for consistency of units and to correct a typographical error.
Redesignate Equation 3 as Equation 5 to provide for the addition of new Equations 3 and 4.
Redesignate Equation 4 as Equation 6 to provide for the addition of new Equations 3 and 4.
Redesignate Equation 5 as Equation 7 to provide for the addition of new Equations 3 and 4.
Redesignate Equation 6 as Equation 8 to provide for the addition of new Equations 3 and 4.
Redesignate Equation 7 as Equation 9 to provide for the addition of new Equations 3 and 4.
Replace ‘‘hourly’’ with ‘‘3-hour’’ in the definition of the new Equation 9 variable ‘‘Opacity limit’’ and replace
‘‘source test runs’’ with ‘‘source test’’ in the definition of the new Equation 9 variable ‘‘Opacityst’’ to clarify
the information required for new Equation 9.
Redesignate the reference to Equation 6 as a reference to Equation 8 to provide for the addition of new
Equations 3 and 4.
Replace ‘‘in § 60.102a(b)(1) shall comply with the requirements in paragraphs (b)(1) through (3) of this section’’ with ‘‘in § 60.102a(b)(1) that uses a control device other than fabric filter or cyclone shall comply with
the requirements in paragraphs (b)(1) and (2) of this section’’ to clarify applicability of the requirements and
remove the reference to a nonexistent paragraph.
Replace ‘‘according to the requirements in paragraph (b)(1)(i) through (iii) of this section’’ with ‘‘according to
the applicable requirements in paragraphs (b)(1)(i) through (v) of this section’’ to clarify and correct paragraph reference.
Replace ‘‘alterative’’ with ‘‘alternative’’ to correct the use of an incorrect word.
Replace ‘‘Except as provided in paragraph (i)(7) of this section, all rolling 7-day periods’’ with ‘‘All rolling 7day periods’’ to remove the reference to a nonexistent paragraph.
Replace ‘‘320 ppmv H2S’’ with ‘‘300 ppmv H2S’’ to make the span value for a H2S monitor consistent with the
span value in 40 CFR part 60, subpart J.
Replace ‘‘the information described in paragraph (e)(6) of this section’’ with ‘‘the information described in
paragraph (c)(6) of this section’’ to correct the reference to a nonexistent paragraph.
60.104a(d)(4)(ii) ...........................
60.104a(d)(4)(iii) ..........................
60.104a(d)(4)(v) ...........................
60.104a(d)(8) ...............................
60.104a(f)(3) ................................
60.104a(h)(5)(iv) ..........................
60.105a(b) ...................................
60.105a(b)(1) ...............................
60.105a(b)(1)(ii)(A) ......................
60.105a(i)(5) ................................
60.107a(a)(2)(i) ............................
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60.108a(d)(5) ...............................
IV. Summary of Significant Comments
and Responses
As previously noted, we received a
total of 22 comments addressing the
proposed amendments. These
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comments were received from
refineries, industry trade associations,
consultants, state and local
environmental and public health
agencies, environmental groups and
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members of the public. Brief summaries
of the major comments and our
complete responses to those comments
are included in the following sections.
A summary of the remainder of the
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comments received during the comment
period and responses thereto, as well as
more detailed summaries of the
comments addressed in this preamble,
can be found in Standards of
Performance for Petroleum Refineries:
Background Information for Final
Amendments—Summary of Public
Comments and Responses, which is
included in the docket for the final
amendments (Docket ID No. EPA–OAR–
HQ–2007–0011). The docket also
contains further details on all the
analyses summarized in the responses
below.
In responding to the public
comments, we re-evaluated the cost and
emission reduction impact estimates of
some of the control options and reevaluated the related BSER
determinations. In our BSER
determinations, we took all relevant
factors into account consistent with
other agency decisions.
A. Process Heaters
Comment: Commenters stated that
new forced draft process heaters cannot
meet the proposed emissions limit of 40
ppmv NOX, so the EPA should revise
the emissions limits for new forced draft
process heaters to be the same as the
limit for modified and reconstructed
forced draft process heaters (60 ppmv
NOX). One commenter referenced a
general technical document written by a
process heater burner manufacturer
regarding a new forced draft process
heater at their refinery to support the
assertion that new process heaters
cannot meet the proposed limit without
selective catalytic reduction or other
add-on controls. Another commenter
also requested higher emissions limits
for new forced draft process heaters
with air preheat.
Response: The commenters provided
only limited and theoretical data to
support their argument that new forced
draft process heaters cannot meet the 40
ppmv (or 0.040 lb/MMBtu) NOX
emissions limit. Specifically, the John
Zink white paper cited by the
commenter (submitted as an attachment
to Docket Item No. EPA–HQ–OAR–
2007–0011–0296) stated only that the 40
ppmv emissions limit could not be
‘‘guaranteed’’ for a new forced draft
process heater, based on the design
conditions, which included air preheat.
Actual NOX performance data for that
commenter’s new forced draft process
heaters are not available, as those
particular process heaters are not yet
operational. As such, the actual
performance of these forced draft
process heaters is still in question.
However, we acknowledge that we only
have data for one new forced draft
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process heater without air preheat that
is currently operating that could meet a
40 ppmv NOX emissions limit on a 365day average. We conducted additional
data evaluations to determine
appropriate limits and averaging times
for all process heaters at normal
operating conditions while considering
this and other public comments we
received. As part of the data analysis
effort, we obtained a year’s worth of
hourly CEMS data for the new forced
draft process heater without air preheat
capable of meeting 40 ppmv on a 365day average. As discussed later in this
section, our analysis of the additional
data that we obtained following the
proposal supported revising all NOX
emissions limits to be on a 30-day
average basis. The data indicate that the
30-day averages for the new forced draft
process heater without air preheat
capable of meeting 40 ppmv on a 365day average exceeded 40 ppmv 15
percent of the time, but none of the 30day averages exceeded 60 ppmv NOX.
Consequently, we are raising the NOX
emissions limit (while concurrently
reducing the averaging time) for all new
forced draft process heaters to be
equivalent to the emissions limit for
modified and reconstructed forced draft
process heaters (i.e., 60 ppmv or 0.060
lb/MMBtu with a 30-day averaging
period). Furthermore, based on the
information provided by the
commenters, as well as the available
performance data for existing forced
draft process heaters with air preheat
that have been retrofitted with ultra-low
NOX burners, we also conclude that the
60 ppmv (or 0.060 lb/MMBtu) on a 30day rolling average basis adequately
accommodates forced draft process
heaters that use air preheat. Based on
our review of CEMS data for new and
retrofitted forced draft process heaters,
we conclude that 60 ppmv (or 0.060 lb/
MMBtu) on a 30-day rolling average
basis is BSER for new, reconstructed or
modified forced draft process heaters.
(For additional details, see Revised NOX
Impact Estimates for Process Heaters, in
Docket ID No. EPA–HQ–OAR–2007–
0011.)
Comment: Commenters asserted that
the heating value-based emissions limits
(i.e., the limits in units of lb/MMBtu)
should be numerically equivalent to the
concentration-based emissions limits
(e.g., 40 ppmv should be equivalent to
0.040 lb/MMBtu rather than 0.035 lb/
MMBtu).
Response: In August 2008, Industry
Petitioners provided the EPA with
suggestions for revising the process
heater standards (Docket Item No. EPA–
HQ–OAR–2007–0011–0257). One of
their recommendations was to include
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emissions limits based on heating value
(lb/MMBtu) to account for hydrogen
content variations in the fuel gas. They
suggested that, on an annual basis, most
natural draft process heaters could meet
0.035 lb/MMBtu and all other process
heaters could meet 0.055 lb/MMBtu. We
evaluated these suggested emissions
limits and determined that they were
reasonably equivalent to the
concentration-based limits we were
proposing. We also requested comment
on their use and their equivalency, as
described in the preamble to the
proposed amendments (see 73 FR
78527). Industry commenters now assert
that the emissions limit numerically
equivalent to the 40 ppmv concentration
limit is 0.040 lb/MMBtu and the
emissions limit numerically equivalent
to the 60 ppmv concentration limit is
0.060 lb/MMBtu.
We note that, as discussed in the
preamble to the proposed amendments,
the exact conversion from ppmv to lb/
MMBtu depends on the hydrogen
content of the fuel gas. However, our
calculations generally support the more
direct numerical conversion suggested
by commenters over the typical range of
hydrogen concentrations expected in
the fuel gas (see Revised NOX Impact
Estimates for Process Heaters, in Docket
ID No. EPA–HQ–OAR–2007–0011).
Therefore, we are finalizing heating
value-based emissions limits of 0.040
lb/MMBtu and 0.060 lb/MMBtu for
natural draft process heaters and forced
draft process heaters, respectively,
based on direct numerical conversions
from the concentration-based emissions
limits.
We are also clarifying that the owner
or operator must demonstrate that the
process heater is in compliance with
either the applicable concentrationbased or heating value-based NOX limit.
The heating value-based NOX emission
rate is calculated using the oxygen (O2)based F factor, which is the ratio of
combustion gas volume to heat input.
Ongoing compliance with this NOX
emissions limit is determined using a
NOX CEMS and at least daily sampling
of fuel gas heat content or composition
to calculate a daily average heating
value-based emissions rate, which is
subsequently used to determine the 30day average.
Specifically, if the F factor is
determined at least daily, the owner or
operator may elect to calculate both a
30-day rolling average NOX
concentration (ppmv, dry basis,
corrected to 0-percent excess air) and a
30-day rolling average NOX emission
factor (in lb/MMBtu) and demonstrate
that the process heater is in compliance
with either one of these limits. For most
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fuel gas systems, the alternative
emissions limits are expected to be
identical; however, there may be
instances where a process heater may be
complying with one of the emissions
limits and not the other. For example,
a process heater combusting fuel gas
with very high hydrogen content may
have an average NOX concentration
above the 60 ppmv limit, but below the
0.060 lb/MMBtu limit, largely due to the
concentration limit being determined on
a dry basis (and understanding that the
combustion of hydrogen produces only
water and not carbon dioxide). Provided
that the appropriate monitoring is
conducted, an affected source would
only be out of compliance if it exceeds
both the concentration-based limit and
the heating value-based limit at the
same time. However, to have the option
to determine compliance with the
alternative heating value-based
emissions limit, the refinery owner or
operator must, at least daily, determine
the F factor (dry basis) for the fuel gas
according to the monitoring provisions
in 40 CFR 60.107a(d). If the F factor is
not determined at least daily, the
heating value-based alternative cannot
be used. Generally, fuel gas heating
value is important to the overall
operation of refinery boilers and process
heaters; as such, refiners maintain their
fuel gas within an operating range that
they need to fire these sources, often by
mixing with natural gas, etc., so we
anticipate that most, if not all, refiners
will already have this information
available on a daily basis.
Comment: Several commenters
addressed the need for the rule to
address turndown, which is a period of
time when process heaters are firing
below capacity. Commenters stated that
during these periods, the NOX
concentrations will likely be above the
emissions limits, but the mass of NOX
emissions is no greater than when the
heater is operating at full capacity
because the lower firing rate results in
a lower exhaust flow rate. Commenters
noted that turndown conditions could
exist for extended periods, so special
provisions are needed for these
conditions. Commenters requested a
mass-based emission rate (lb/MMBtu
limit multiplied by the heater’s rated
capacity) that would apply when the
process heater is firing at less than full
capacity (some commenters suggested
50 percent of capacity; one commenter
suggested 70-percent capacity as a
cutoff). One commenter also noted that
process heaters must often operate at
higher O2 levels during turndown and
requested that the proposed maximum
O2 operating limit not apply when small
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furnaces that are not required to install
CEMS are firing at less than full
capacity.
Response: In our proposed
amendments, we provided a longer
averaging time (365-day average) so that
short periods of turn-down would not
significantly affect the overall
performance of the unit. However,
according to the commenters, the longer
averaging time does not adequately
address turndown conditions.
Therefore, we re-evaluated the available
data, including our existing data and
additional data provided by the
industry, to determine the appropriate
emissions limits during different types
of operation, including turndown. The
additional data provided by Industry
and our evaluation of those data are
included in the docket for the final
amendments (Docket ID No. EPA–OAR–
HQ–2007–0011). Based on our analysis
of the data (described in greater detail
in the next paragraph), we concluded
that a 30-day averaging period is
appropriate for the NOX emission limits
under most operating scenarios.
Upon examination of all available
CEMS data, we determined that, for
periods of normal operation (i.e., firing
at 50 percent or more of design
capacity), the proposed NOX emissions
limits of 40 and 60 ppmv were not
achievable for all process heaters using
a 24-hour averaging period (the
averaging period included in the final
June 2008 rule). From the available data,
short-term fluctuations in the NOX
concentrations of process heaters using
ultra-low NOX burners caused them to
exceed a 24-hour average limit
somewhat frequently, but a 30-day
average provided adequate time to
average out the short-term fluctuations.
We note that a few of the process
heaters operated at relatively high
excess O2 concentrations at normal
conditions (i.e., at exhaust O2
concentrations of 6 percent or more).
These units had periods of excess
emissions above the 30-day average
emission limits, but we rejected the
performance of these process heaters as
BSER because of the high exhaust O2
concentrations for these units during
normal (i.e., non-turndown) firing rates.
That is, these process heaters were not
being operated optimally for reducing
NOX emissions. Furthermore, when
these process heaters were operated at
the lower range of exhaust
concentrations for the unit (although
generally higher than what would be
considered optimal excess O2
concentrations for reducing NOX
emissions), the process heater could
meet the applicable 40 or 60 ppmv
emissions limit on a 30-day averaging
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56435
period. Based on our review of CEMS
data for process heaters with ultra-low
NOX burners that operated at excess O2
concentrations less than 6 percent (i.e.,
operated in a manner consistent with
proper low NOX burner operation), all
such process heaters could comply with
the final NOX emissions limits on a 30day average basis. Consequently, we
revised the basic emissions limits to be
on a 30-day average.
As described previously in this
section, we conclude that the applicable
40 or 60 ppmv emissions limit on a 30day averaging period is achievable for
process heaters during periods of
normal operation. Our next step was to
evaluate the achievability of the
emissions limits during turndown
conditions and alternative approaches
for establishing emissions limitations
where necessary. The following
paragraphs describe our analysis of the
data, including our evaluation of
alternative methods for accommodating
turndown conditions and our rationale
for providing the site-specific
alternative for extended turndown
conditions.
There were very limited CEMS data
available for process heaters operating
under turndown conditions (i.e., firing
below 50 percent of design capacity).
However, two general trends were
observed in the CEMS data that were
available: (1) Typical exhaust O2
concentrations increase at lower firing
rates; and (2) exhaust NOX
concentrations (corrected to 0-percent
excess O2) increase with increasing O2
concentration (regardless of firing rates).
These data, along with the need to
operate the process heater at higher O2
concentrations during low firing rates to
maintain flame stability, suggest that an
alternative NOX emissions limit could,
in some instances, be needed to address
extended turndown conditions
(turndown events lasting a majority of
the 30-day averaging time). As such, we
considered alternative compliance
options to address turndown conditions.
One alternative compliance option
considered to address turndown was a
mass-based NOX emissions limit that
would be equivalent to the mass of NOX
emitted from a unit meeting the 0.040
(or 0.060) lb/MMBtu limit while firing
at 50 percent of capacity, as suggested
by commenters. However, for most units
for which CEMS data are available, the
alternative mass-based emissions limit
did not improve the ability of the
process heater to meet the emissions
limit. We note that most of the process
heaters were able to meet the applicable
concentration-based emissions limit
(40/60 ppmv) or the heating value-based
(0.040/0.060 lb/MMBtu) emissions limit
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during turndown. Therefore, the issue
appears to be limited to a few of the
process heaters that must operate at
relatively high excess O2 concentrations
during turndown conditions. For these
units, the alternative mass-based
emissions limit that we were
considering rarely, if ever, provided a
means for these units to comply with
the performance standard.
We understand that technology
providers recommend operating process
heaters that are turned down at higher
excess O2 concentrations to improve
flame stability and ensure safe operation
of the process heater; however, based on
the information provided by the
technology providers, there is still an
optimal excess O2 concentration at
which flame stability is achieved while
minimizing NOX formation. That is,
even when a process heater is operating
at less than 50-percent design capacity,
excess O2 concentrations should still be
controlled to minimize NOX formation
within the safe operating constraints to
maintain flame stability. We do not have
specific data on process heaters that are
near, but below, the concentration
emissions limits when firing above 50percent capacity, but cannot meet the
concentration limit when firing below
50-percent capacity, so we have no data
that show that process heaters operating
at less than 50-percent design capacity
and controlling excess O2
concentrations cannot meet the
emissions limits. However, we
acknowledge that the correlations with
firing rates and O2 and/or NOX
concentrations and the need for higher
O2 concentrations to maintain flame
stability generally support the
commenter’s argument that a few
marginally compliant process heaters
will have difficulty meeting the basic
emissions limit when the unit is turned
down. As such, we acknowledge that
there may be periods of turndown in
which a process heater is operating as
recommended, but may be unable to
meet the concentration or heating valuebased emissions limits in the final rule,
especially when the unit is operated at
turndown for extended periods (e.g., for
20 days or more compared to the 30-day
averaging time). As the need for an
alternative limit appears to be limited to
a few process heaters and the optimal
O2 concentration is expected to vary,
based on fuel gas composition, we
determined that a site-specific
emissions limit was the best approach to
account for these extended turndown
conditions. As such, the final rule
provides owners and operators that have
a process heater operating in turndown
for an extended period of time the
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option of developing a site-specific
emissions limit that would apply to
those operating conditions and
requesting approval from the
Administrator to use that limit.
For process heaters between 40 and
100 MMBtu/hr capacity that do not
install a NOX CEMS, turndown is also
expected to be an issue with respect to
achieving the O2 operating limit. As
described above, higher O2
concentrations are generally needed to
maintain flame stability at low firing
rates. To address potential turndown
compliance issues with the O2 operating
limit, we have provided an allowance
for process heater owners or operators to
develop an O2 operating curve to
provide different O2 operating limits
based on the firing rate of the process
heater. If a single O2 operating limit is
established, it must be determined when
the process heater is being fired at 70
percent or more of capacity (i.e., far
from turndown conditions). For process
heaters that routinely operate at less
than 50 percent of design capacity and
require additional O2 to maintain flame
stability, a separate O2 operating limit
should be established for turndown by
conducting a second performance test
while the unit is operating at less than
50 percent of capacity. Additional
performance tests can be conducted to
develop O2 operating limits for
additional operating ranges.
Comment: Several commenters
requested that the EPA revise the
emissions limits for co-fired process
heaters or remove the limits for co-fired
process heaters from this rulemaking
and address them at a later date due to
lack of sufficient data to set an
achievable emissions limit. One
commenter provided a white paper to
support higher emissions limits.
Commenters also asserted that the
averaging time for the weighted average
emission rate should be extended to 365
days. One commenter noted that the
notation ‘‘ENOx,hour’’ in Equation 3 was
confusing since the purpose of the
equation was to determine the daily
emission rate.
Response: The final June 2008 rule
included only one emissions limit for
all co-fired process heaters, and
Industry Petitioners asserted that
differences in the configuration and
operation of different types of process
heaters warranted different emissions
limits. The proposed amendments
introduced two specific emissions limits
for co-fired process heaters, one based
on vendor guarantees for the burners
and one based on an average NOX
concentration for a combination of fuel
gas and fuel oil. We note that, for
purposes of this rule, a co-fired process
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heater is defined as a process heater that
employs burners that are designed to be
supplied by both gaseous and liquid
fuels. In other words, co-fired process
heaters are designed to routinely fire
both oil and gas in the same burner.
These do not include burners that are
designed to burn gas, but have
supplemental oil firing capability that is
not routinely used (i.e., emergency oil
back-up).
To respond to the comments
requesting higher emissions limits for
co-fired process heaters, we reviewed
the white paper provided by one
commenter (submitted as an attachment
to Docket Item No. EPA–HQ–OAR–
2007–0011–0308), as well as additional
burner emissions test data provided by
another commenter 5 (conducted under
well-controlled conditions using best
available ultra-low NOX burner
technologies at the manufacturer’s
testing facility). This information
indicates that, for co-fired natural draft
process heaters, a daily average
emissions limit calculated based on a
limit of 0.06 lb/MMBtu for the gas
portion of the firing and 0.35 lb/MMBtu
for the oil portion of the firing is
achievable. Similarly, the information
indicates that, for co-fired forced draft
process heaters, a daily average
emissions limit calculated based on a
limit of 0.11 lb/MMBtu for the gas
portion of the firing and 0.40 lb/MMBtu
for the oil portion of the firing is
achievable. As noted above, these values
are based on burner performance tests,
which are considered a better source of
information than the vendor guarantees
that were relied upon to develop the
proposed emissions limit. Therefore, we
are revising the NOX emissions limits
for co-fired process heaters to those
described above. We note that we have
revised the concentration-based NOX
emissions limits to be on a 30-day
average basis (same as the limits for gasfired process heaters). We have also
revised the nomenclature of the daily
average emissions limit in Equations 3
and 4 (proposed Equation 3) to be clear
that we intend the limit to be
determined on a daily basis rather than
on an hourly basis.
We also note that the burner
performance tests were conducted in a
controlled environment at the burner
manufacturer’s full-scale facilities.
While it is incumbent on the owner or
operator of an affected process heater to
control certain operating parameters,
such as excess O2 concentrations, to the
5 The commenter providing this data asserted that
it is CBI. We will follow our CBI regulations in 40
CFR part 2 in handling this data. The data has been
placed in the docket, but is not publicly available.
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extent possible, we recognize that the
performance limits in the final
amendments are based on limited data,
none of which are direct test data for a
co-fired process heater operated at a
petroleum refinery. We conclude that
the low-NOX burner technologies exist,
are demonstrated and are cost effective
for co-fired process heaters and they are,
therefore, BSER for co-fired process
heaters. However, as the performance
limits are based on limited operational
data, we also conclude that it is
reasonable to provide an alternative,
site-specific limit in the event that
factors outside the influence of the
burner design and operation (such as
nitrogen content in the fuel oil) suggests
the emission limits in the final rule are
inappropriate for a specific application.
Consequently, co-fired process heaters
that cannot meet the limits specified
above, can request approval for a sitespecific emissions limit, as allowed
above, for process heaters that operate
for extended periods under turndown.
B. Flares
Comment: Several commenters
asserted that routine connections to a
flare should not be considered
modifications of the flare because they
do not change the maximum physical
capacity of the flare and do not
generally increase emissions. One
commenter asserted that the 40 CFR part
60, subpart A General Provisions in 40
CFR 60.14 can and should apply to
flares, so a special modification
provision for flares in 40 CFR part 60,
subpart Ja is unnecessary. Commenters
noted that some connections to the flare
have the primary purpose of reducing
emissions, which has been excluded
under 40 CFR 60.14(e)(5), a paragraph
that is not limited to pollutants ‘‘to
which the standard is applicable.’’ One
commenter noted that a single project
may remove some connections and add
others such that the net emissions could
actually be reduced. Another
commenter asserted that an increase in
flow should not be considered a
modification because flow is not a
regulated pollutant.
Instead, commenters asserted that the
modification provision for a flare should
focus on physical and operational
changes that increase emissions from
the flare. One commenter suggested that
the EPA should focus the flare
modification provision on connections
that provide a primary/routine flow
from a process unit to the flare. Other
commenters suggested that the flare
modification provision should be
focused on VOC and SO2 emissions and
should only include connections that
result in a net increase of those
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pollutants emitted ‘‘during normal
operations’’ and connections that cause
an increase in the total volume of gas
containing VOC or sulfur compounds
under standard conditions that could
reach the flare.
Response: The agency made a
conscious decision to promulgate a
separate provision for a flare
modification in 40 CFR part 60, subpart
Ja (see 40 CFR 60.14(f)) because flares
are operated differently from other
refinery process units, making it
difficult to apply the modification
provision in the General Provisions (40
CFR 60.14) to them. The physical
capacity of a flare is based on the
amount of gas potentially discharged to
a flare as a result of emergency relief.
Refiners frequently make connections to
existing flares that result in emissions
increases at the flares, but may never
approach the physical capacity of the
flare system. Contrary to commenters’
assertions, the flare modification
provision in 40 CFR 60.100a(c) does
meet the statutory definition of
‘‘modification’’ in CAA section
111(a)(4), which is ‘‘any physical
change in, or change in the method of
operation of, a stationary source which
increases the amount of any air
pollutant emitted by such source or
which results in the emission of any air
pollutant not previously emitted.’’ It is
axiomatic that the connections to the
flare described in 40 CFR 60.100a(c)
qualify as physical or operational
changes to the flare. Additionally, we
explained in the proposed rule how
these connections also resulted in
emissions increases from the flare (see
73 FR 78529). Thus, these types of new
connections of refinery process units
(including ancillary equipment) and
fuel gas systems to the flare qualify as
a ‘‘modification’’ of the flare and trigger
subpart Ja applicability for the flare.
Those connections we identified that
do not increase emissions from the flare
were specifically excluded from
triggering 40 CFR part 60, subpart Ja
applicability under this same provision
(see 40 CFR 60.100a(c)(1)). Specifically,
we proposed on December 22, 2008, that
the following types of connections to a
flare would not be considered a
modification of the flare: (1)
Connections made to install monitoring
systems to the flares; (2) connections
made to install a flare gas recovery
system; (3) connections made to replace
or upgrade existing pressure relief or
safety valves, provided the new pressure
relief or safety valve has a set point
opening pressure no lower and an
internal diameter no greater than the
existing equipment being replaced or
upgraded; and (4) replacing piping or
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moving an existing connection from a
refinery process unit to a new location
in the same flare, provided the new pipe
diameter is less than or equal to the
diameter of the pipe/connection being
replaced/moved. While we agree that
there may be other connections to a flare
that would not result in an emissions
increase from the flare (see response to
the next comment for specific details),
we disagree with the commenters that
the flare modification provision should
be further limited beyond what is
already provided in the provision.
We disagree with commenters that we
must consider the ‘‘net’’ emissions from
the process unit and the flare when
determining whether a flare is modified.
The affected facility is the flare and does
not include the process units that are
tied into the flare header system. See
Asarco v. EPA, 578 F.2d 319, 325 (D.C.
Cir. 1978) (holding that emission
increases had to be determined based on
emissions from the affected facility). We
also disagree that a modification
determination should be limited to
emissions increases of VOC or SO2.
Flares are known to emit VOC, SO2,
carbon monoxide (CO), PM and NOX, as
well as other air pollutants, all of which
are relevant when determining whether
a flare has been modified. See CAA
section 111(a)(4). That is, we consider
the standards for flares to be emission
standards for VOC, SO2, CO, PM and
NOX. See, generally, 73 FR 35838,
35842, 35854–35856 (June 24, 2008); 73
FR 78522, 78533 (December 22, 2008),
as well as Table 4 of this preamble.
Using the flare to control VOC
emissions at other refinery process units
will increase CO, PM and NOX
emissions from the flare and are,
therefore, considered modifications of
the flare, even if there is a net reduction
in VOC emissions at the refinery.
In evaluating whether a flare has been
modified, we consider increases in flow
to the flare to be directly indicative of
increased emissions from the flare.
While we agree that ‘‘flow’’ is not a
pollutant, we evaluated flow limits as a
means to reduce SO2, VOC, CO, NOX
and other emissions from the flare. The
emissions from the flare are very
difficult, if not impossible, to measure
accurately, but flow to the flare can be
measured, and the flow to the flare
generates SO2, VOC, CO, PM, NOX and
other emissions. Therefore, a physical or
operational change to a flare that causes
an increase of flow to the flare will
increase emissions of at least one of
these pollutants and is considered a
modification of the flare.
Comment: Many commenters
responded to the EPA’s request for
comment on types of connections that
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do not result in an increase in emissions
from a flare. The commenters suggested
numerous specific connections that
should not be considered modifications,
including:
(1) Connections made to upgrade or
enhance (not just to install) a flare gas
recovery system;
(2) Connections made for flare gas
sulfur removal;
(3) Connections made to install backup equipment;
(4) Flare interconnects;
(5) All emergency pressure relief
valve connections from existing
equipment;
(6) Connections of monitoring system
purge gases and analyzer exhausts or
closed vent sampling systems;
(7) Purge and clearing vapors, block
and bleeder vents and other
uncombusted vapors where the flare is
the control device;
(8) Connections made to comply with
other federal, state or local rules where
the flare is the control device;
(9) Connections of ‘‘unregulated
gases’’ such as hydrogen, nitrogen,
ammonia, other non-hydrocarbon gases
or natural gas or any connection that is
not fuel gas;
(10) New connections upstream of an
existing flare gas recovery system,
provided the new connections do not
compromise or exceed the flare gas
recovery system’s capacity;
(11) Any new, moved or replaced
piping or pressure relief valve
connections that do not result in a net
increase in emissions from the flare,
regardless of piping or pressure relief
valve size;
(12) Vapors from tanks used to store
sweet or treated products;
(13) Temporary connections for
purging existing equipment, as these are
essentially ‘‘existing’’ connections; and
(14) Connections of safety
instrumentation systems (SIS) described
under Occupational Safety and Health
Administration (OSHA) process safety
standards at 29 CFR 1910.119, the EPA’s
risk management program at 49 CFR 68
and/or American National Standards
Institute (ANSI)/International Society of
Automation (ISA)-84.00.01–2004.
Response: We carefully reviewed the
commenters’ suggested changes to the
flare modification provision to
determine whether there are additional
connections that should not be
considered modifications to the flare.
We agree that the first four connections
in the commenters’ list should not be
considered modifications of a flare.
Projects to upgrade or enhance
components of a flare gas recovery
system (e.g., addition of compressors or
recycle lines) will improve the
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operation of the flare gas recovery
system, and connections to these
additional components will not result in
increased emissions. Connections made
for removal of sulfur from flare gas (Item
2 above) will generally result in a slight
decrease in volumetric flow and a large
decrease in emissions of SO2.
Connections made to install back-up or
redundant equipment (Item 3 above),
such as a back-up compressor, will
result in fewer released emissions if
there is a malfunction in the main
equipment.
The request to exclude flare
interconnections (Item 4 above) is a
complicated issue because
interconnecting two separate flares
alters what we consider to be the
affected facility. The definition of
‘‘flare’’ specifically includes the flare
gas header system as part of the flare.
Prior to interconnecting the flares,
presumably each flare header system is
independent, and there would be two
separate ‘‘flares,’’ each of which could
potentially be an affected facility subject
to 40 CFR part 60, subpart Ja. However,
because the flare includes the flare
header system, we consider that an
interconnected flare system is a single
affected facility, and we have amended
the definition of ‘‘flare’’ for clarity. We
agree that interconnections between
flares will not alter the cumulative
amount of gas being flared (i.e.,
interconnecting two flares does not
result in an emissions increase relative
to the two single flares prior to
interconnection). We also see cases
where the emissions from a single flare
tip will likely be reduced due to the
flare interconnect. For example, when a
large release event occurs, this gas will
now flow to both of the interconnected
flares rather than a single flare. The
maximum emission rate for the original
single flare actually decreases, while the
combined emissions from both flares is
the same quantity as prior to the
interconnection. Considering this, we
agree that the interconnection of two
flares does not necessarily result in a
modification of the flare and we have
specifically excluded flare
interconnections from the modification
provisions.
However, we also clarify in this
response that when a flare that is subject
to 40 CFR part 60, subpart Ja is
interconnected with a flare that is not
subject to subpart Ja, then the resulting
interconnected flare is subject to subpart
Ja. That is, the only case in which an
interconnection between two (or more)
flares results in a combined,
interconnected flare that is not subject
to subpart Ja is when none of the
original individual flares were subject to
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subpart Ja. Additionally, we note that if
a new connection is made to the
interconnected flare, then the flare
(including each individual flare tip
within the interconnected flare header
system) is modified and becomes an
affected facility subject to subpart Ja.
While we agree that connections that
do not increase the emissions from the
flare should not trigger a modification,
we disagree with the commenter that
their other suggested connections do not
increase the flare’s emissions at the time
gases are discharged via the new
connection. Each of the commenters’
suggestions is discussed in the
following paragraphs.
We previously proposed an
exemption for emergency pressure relief
valve connections from existing
equipment (Item 5 above) if they replace
or upgrade existing equipment and do
not increase the instantaneous release
rate to the flare (i.e., the new pressure
relief valve has a pressure set point and
diameter no greater than the equipment
being replaced). As stated previously in
this preamble, we are finalizing that
amendment, as proposed. However, new
connections, even if they are made to
‘‘existing equipment,’’ will result in an
increase in flow to the flare during
periods of process upset that cause the
pressure relief valve to open.
Connections of monitoring system
purge gases and analyzer exhausts or
closed vent sampling systems (Item 6
above) will increase the emissions from
the flare. Similarly, connections of
purge and clearing vapors and block and
bleeder vents (Item 7 above), also trigger
a modification of the flare because the
increase of gas flow to the flare will
increase the emissions from the flare.
We recognize that connections to a
flare may be made to comply with other
federal, state or local rules where the
flare is an emissions control device
(Item 8 above). In fact, nearly all flares
could be considered ‘‘control devices.’’
We agree that using a flare as an
emissions control device is preferable to
venting the process unit to the
atmosphere. However, while using the
flare as an emissions control device
does decrease emissions from the
process unit being controlled, the
increase of gas flow to the flare will
increase the emissions from the flare.
Therefore, a connection from a process
unit to a flare for use as an emissions
control device results in a modification
of that flare.
Comments suggesting that
connections of ‘‘unregulated gases’’
such as hydrogen, nitrogen, ammonia,
other non-hydrocarbon gases or natural
gas or connections that are not ‘‘fuel
gas,’’ should not be considered a
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modification of the flare (Item 9 above)
are in conflict with the statutory
definition of ‘‘modification.’’ Each of the
streams mentioned by the commenter,
when directed to a flare, will increase
emissions of at least one pollutant
(either PM, CO or NOX) from the flare
(all of which the standard is intended to
reduce). That is, we reiterate that we
consider the standards for flares to be
emission standards for VOC, SO2, CO,
PM and NOX. As such, we do not agree
that the types of gas streams suggested
by the commenters should be exempt
from the modification determination.
New connections upstream of an
existing flare gas recovery system (Item
10 above) will increase the likelihood of
an event that would cause an
exceedance of the flare gas recovery
system’s capacity (even if the new
connections ‘‘do not exceed the flare gas
recovery system’s capacity’’ under
normal conditions), and the amount of
gases sent to the flare would increase as
a result of such an event, thereby
increasing the emissions from the flare.
We reiterate that we proposed an
exemption for any moved or replaced
piping or pressure relief valve
connections of the same size. However,
we disagree with the commenter’s
suggestion that any ‘‘new, moved, or
replaced piping or pressure relief valve
connections that do not result in a net
increase in emissions from the flare
regardless of piping or pressure relief
valve size’’ should be exempted (Item 11
above). The premise of the suggested
amendment is that new or larger
connections somehow will not increase
emissions from the flare. We have
discussed new connections previously,
so we will concentrate on the
‘‘regardless of piping or pressure relief
valve size’’ comment in this paragraph.
First, the size of the pressure relief valve
or piping does correlate to the discharge
rate to the flare, with larger pressure
relief valves or larger diameter piping
allowing higher discharge rates to the
flare at a given pressure. In fact, larger
pressure relief valves and larger
diameter pipes are specifically designed
to allow higher flow rates to the flare.
Second, higher flow rates will lead to
higher emission rates. For a pressure
relief event that occurs for several
hours, the flow rate to the flare during
the first hour of relief using the larger
pressure relief valve or larger diameter
piping will be larger than the flow rate
experienced using the smaller pressure
relief valve or smaller diameter piping
and will result in higher emissions from
the flare. Therefore, we reject the notion
that larger diameter pipes and larger
pressure relief valves do not increase
the emissions rate from the flare during
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a release event. We are finalizing the
proposed exemptions for moved or
replaced piping or pressure relief valves
with the size and design restrictions for
the new piping or pressure relief valves
as proposed on December 22, 2008.
Commenters suggested that
connections of vapors from tanks used
to store sweet or treated products (Item
12 above) should not be modifications
because those gas streams have less than
162 ppmv H2S. We reiterate that SO2 is
not the only pollutant emitted from
flares and that the additional flow of
sweet gases will increase the emissions
of at least one pollutant from the flare,
so we are not exempting these types of
connections to the flare from the 40 CFR
part 60, subpart Ja flare modification
provision. However, we have amended
the sulfur monitoring requirements for
flares to exempt vapors from tanks used
to store sweet or treated products from
the flare sulfur monitoring
requirements. This monitoring
exemption is justified because it is not
needed for the purposes of a root cause
analysis or other compliance purpose.
For these sweet vapors, the flow rate
root cause analysis threshold will be
exceeded well before the SO2 root cause
analysis threshold.
We carefully considered temporary
connections for purging existing
equipment (Item 13 above), but we
failed to see how these temporary
connections are essentially ‘‘existing
connections.’’ According to the
commenters, ‘‘maintenance gases have
been routed in some form or other to the
flare for years, and the temporary tie-in
to accomplish that is not a change and
is not an increase in emissions when
viewed from a before and after
perspective.’’ If the connections already
exist, then opening an existing valve to
allow for this type of purging would not
trigger a flare modification. If the
connection is being relocated and the
piping used is the same diameter as the
pre-existing connection, then this
scenario is adequately covered by the
proposed exclusion for relocated
connections. However, if a new
connection is made specifically to purge
an existing piece of equipment, this
purge gas unequivocally represents
additional gas flow sent to the flare that
did not exist and could not exist prior
to the connection being made. Again,
we consider that the increase in gas flow
to the flare will result in an increase in
emissions of at least one pollutant from
the flare. As such, no exemption is
provided for new connections to
existing equipment, regardless if these
connections are temporary or
permanent. We also find that these
types of flows should be expressly
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56439
considered in the flare management
plan and that flaring from these
‘‘temporary’’ connections should be
minimized to the extent practicable.
The impact of connections of SIS
described under OSHA process safety
standards at 29 CFR 1910.119, the EPA’s
risk management program at 49 CFR 68
and ANSI/ISA–84.00.01–2004 (Item 14
above) should be evaluated on a caseby-case basis to determine whether
these connections result in a flare
modification. We expect that, if these
connections are made for flare
monitoring purposes, these connections
are already excluded in the exemption
for flare monitoring systems. If the
‘‘SIS’’ are process unit analyzers and the
new connections are being made to
connect the analyzer exhaust to the
flare, these connections would be
considered a modification, as previously
discussed. The commenter may also be
referring to new connections for
additional pressure relief valves
identified in the safety reviews required
by the cited rules, which we would
consider to be a modification of the
flare.
Following all of the above review and
analysis, we are finalizing three of the
connections, as proposed, adding three
of the connections requested by
commenters and revising one of the
proposed connections as requested by
commenters in 40 CFR 60.100a(c)(1).
Thus, the following seven types of
connections are not considered a
modification of the flare:
(1) Connections made to install
monitoring systems to the flare.
(2) Connections made to install a flare
gas recovery system or connections
made to upgrade or enhance
components of a flare gas recovery
system (e.g., addition of compressors or
recycle lines).
(3) Connections made to replace or
upgrade existing pressure relief or safety
valves, provided the new pressure relief
or safety valve has a set point opening
pressure no lower and an internal
diameter no greater than the existing
equipment being replaced or upgraded.
(4) Connections that interconnect two
or more flares.
(5) Connections made for flare gas
sulfur removal.
(6) Connections made to install backup (redundant) equipment associated
with the flare (such as a back-up
compressor) that does not increase the
capacity of the flare.
(7) Replacing piping or moving an
existing connection from a refinery
process unit to a new location in the
same flare, provided the new pipe
diameter is less than or equal to the
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diameter of the pipe/connection being
replaced/moved.
Comment: Several commenters
suggested that de minimis emission
increases and net emission decreases
resulting from new connections to a
flare made to control and combust
fugitive emissions such as leaks from
compressor seals, valves or pumps,
should not be considered modifications
of a flare. One commenter suggested
allowing site-specific exemptions for
connections that do not increase
emissions or that result in a de minimis
emissions increase. However, another
commenter objected to setting a de
minimis emissions increase to
determine whether a change to a flare is
a modification and stated that allowing
a de minimis approach would cause
confusion over the applicability of 40
CFR part 60, subpart Ja because flare
emissions are difficult to estimate.
Response: In the preamble to our
proposed amendments, the EPA
specifically requested comment on
using the de minimis exception in the
flare modification provision. 73 FR
78522, 78529. Industry Petitioners had
suggested some type of de minimis
emissions increase should be allowed
without triggering 40 CFR part 60,
subpart Ja applicability. Id. The EPA
acknowledged that these exceptions are
‘‘permissible but not required’’ under
the modification provision in the CAA.
Id. The EPA also stated: ‘‘We request
comments on a de minimis approach
and on specific changes that may occur
to flares that will result in de minimis
increases in emissions. We also request
comments on the type, number, and
amount of emissions that would be
considered de minimis.’’ Id.
Industry Petitioners continue to
recommend that any emissions
increases resulting from ‘‘routine
connections’’ to the flare system ‘‘will
be de minimis’’ and should not trigger
40 CFR part 60, subpart Ja applicability
at the flare, but they have not provided
the comments or data requested in the
proposal preamble that the EPA could
consider to evaluate the impacts of such
an approach. Docket Item No. EPA–HQ–
OAR–2007–0011–0311 (second
attachment), pg 20. Industry Petitioners
again suggest that the EPA exercise its
authority and ‘‘authorize exceptions
from otherwise clear statutory
mandates’’ by promulgating de minimis
exemptions for the flare modification
provision. Id.; Alabama Power Co. v.
Costle, 636 F.2d 323, 360 (D.C. Cir.
1979). As explained in Alabama Power,
the de minimis exception allows agency
flexibility in interpreting a statute to
prevent ‘‘pointless expenditures of
effort.’’ Id. However, as Industry
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Petitioners recognize, nothing mandates
that the EPA use its de minimis
authority in any given instance, and
courts especially recognize the
significant deference due an agency’s
use of a de minimis exception. Id. at
400; Shays v. Federal Election Com’n,
414 F.3d 76, 113 (D.C. Cir. 2005);
Environmental Defense Fund, Inc. v.
EPA, 82 F.3d 451, 466 (D.C. Cir. 1996);
Ass’n of Admin. Law Judges v. Fed.
Labor Relations Auth., 397 F.3d 957,
961 (D.C. Cir. 2005).
In exercising that discretion, the EPA
must consider the cautionary advice it
received from the Alabama Court
regarding its use of the de minimis
exception: ‘‘EPA must take into account
in any action * * * that this exemption
authority is narrow in reach and tightly
bounded by the need to show that the
situation is genuinely de minimis.’’ Id.
at 361. The Court also noted that
exemptions from ‘‘the clear commands
of a regulatory statute, though
sometimes permitted, are not favored.’’
Id. at 358. The EPA must exercise this
authority cautiously, and only in those
circumstances that truly warrant its
application.
The EPA has found no basis for
promulgating a de minimis exception to
the flare modification provision. Despite
its assertions, Industry Petitioners have
still provided no data to support a
finding that the emissions increases
resulting from the alleged ‘‘routine
connections’’ to a flare system are truly
‘‘trivial or [of] no value.’’ Docket Item
No. EPA–HQ–OAR–2007–0011–0311
(second attachment), pg 20. Without the
requested information showing that ‘‘the
situation is genuinely de minimis,’’
Alabama Power, 636 F.2d at 361 and,
therefore, warrants this kind of
exception, we believe such an
exemption would be inappropriate.
Additionally, Industry Petitioners’
example that ‘‘venting a new small
storage tank to a flare system * * *
easily would cost a typical refinery tens
of millions of dollars’’ since ‘‘the entire
flare system’’ (emphasis in original)
would be subject to subpart Ja is
unavailing for its argument that the EPA
should promulgate a de minimis
exception for the flare modification
provision. Docket Item No. EPA–HQ–
OAR–2007–0011–0311 (second
attachment), pg 21. As the District of
Columbia Circuit specifically states in
Shays, authority for promulgating a de
minimis exception ‘‘does not extend to
a situation where the regulatory
function does provide benefits, in the
sense of furthering regulatory objectives,
but the agency concludes the
acknowledged benefits are exceeded by
the costs.’’ Shays, 414 F.3d 76, 114
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(emphasis added). By focusing solely on
cost, Industry Petitioners are effectively
asking the agency to engage in the type
of cost-benefit analysis prohibited by
the Shays Court. Such cost analyses are
improper in these types of decisions.
Industry Petitioners generally focus
their discussion on VOC emissions and
effectively admit that connecting the
small storage tank to the flare system
increases emissions from the flare (e.g.,
‘‘uncontrolled tank emissions would be
essentially eliminated by combustion in
a flare’’ (Docket Item No. EPA–HQ–
OAR–2007–0011–0311 (second
attachment), pg 21, emphasis added)).
Furthermore, they disregard additional
emissions of NOX and CO resulting from
the combustion of these gases at the
flare. Industry Petitioners also provide
no data quantifying these emissions
increases and, therefore, cannot
demonstrate that they are ‘‘trivial or [of]
no value’’ or, in other words, that the
emissions increases are, in fact, de
minimis. As releases to the flare are
often event driven, one can envision
situations where the release from even
a small storage tank could be significant.
On the other hand, the EPA sees a
substantial environmental benefit in
requiring controls that will reduce the
cumulative emissions from a flare that
becomes subject to 40 CFR part 60,
subpart Ja because of any of these
alleged ‘‘routine connections.’’ Thus,
given the nature of releases to the flare,
we determined that a de minimis
exemption from the modification
provisions for flares is unworkable and
unwarranted.
Comment: One commenter stated that
exempting flares 6 from the H2S
concentration limits during startup,
shutdown and malfunction (SSM)
events is illegal because the CAA
requires continuous compliance with
standards of performance promulgated
under CAA section 111. See CAA
sections 111(a)(1), 302(k). For support,
the commenter cited Sierra Club v. EPA,
551 F.3d 1019 (DC Cir. 2008), in which
the Court stated: ‘‘When sections 112
and 302(k) are read together, then,
Congress has required that there must be
continuous section 112-compliant
standards.’’ The commenter noted that
the Court found that the exemption from
compliance with CAA section 112
standards during SSM events violates
6 The comments submitted referenced ‘‘fuel gas
combustion devices’’ as the affected source when
describing the exemption during SSM events.
However, the exemption only applies to flares. See
40 CFR 60.103a(h). The discussion in this preamble
is, therefore, focused on flares as distinguished from
other types of fuel gas combustion devices that are
required to comply at all times with the H2S
concentration limits in 40 CFR 60.102a(g)(1).
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the CAA because the general duty to
minimize emissions during SSM events
is not a CAA section 112-compliant
standard. The commenter asserted that
the CAA also requires that a section
111-compliant standard that reflects
BSER 7 be in effect at all times for flares.
The commenter further asserted that
work practice standards for flares are
not CAA section 111-compliant
standards because this is not one of
those ‘‘limited instances’’ in which CAA
section 111(h) authorizes such
standards. The commenter stated that
the EPA must show that a standard of
performance for flares is ‘‘not feasible to
prescribe or enforce’’ because ‘‘(A) a
pollutant * * * cannot be emitted
through a conveyance designed and
constructed to emit or capture such
pollutant, or that any requirement for, or
use of, such a conveyance would be
inconsistent with any federal, state or
local law or (B) the application of
measurement methodology to a
particular class of sources is not
practicable due to technological or
economic limitations.’’ See CAA section
111(h)(2). The commenter stated that
neither of these exemptions appear to
apply and the EPA cannot claim that it
is infeasible to promulgate a standard of
performance for flares,8 so the EPA
cannot set a work practice standard for
flares. Thus, the commenter asserted
that a CAA section 111-compliant
standard does not continuously apply to
flares since both the exemption from the
H2S concentration limits during SSM
events and the flare work practice
standards are not lawful under the CAA.
Another commenter disagreed and
provided several reasons why they
believe the EPA may lawfully exempt
flares from the H2S concentration limits
during SSM events. First, the
7 The commenter asserted, without providing
support, that it is not BSER to exempt flares from
the H2S concentration limits during startup and
shutdown events. The commenter also stated that
the EPA, at a minimum, must demonstrate how the
exemption from the H2S concentration limits during
SSM events does, in fact, represent BSER, but the
commenter stated that the EPA has failed to make
this demonstration.
8 The commenter cited the EPA’s rationale for
proposing work practice standards for flaring in
which we state: ‘‘It is not feasible to prescribe or
enforce a standard of performance for these sources
because either the pollution prevention measures
eliminate the emission source, so that there are no
emissions to capture and convey, or the emissions
are so transient, and in some cases, occur so
randomly, that the application of a measurement
methodology to these sources is not technically and
economically practical.’’ 72 FR 27178, 27194–27195
(May 14, 2007). In response, the commenter stated:
‘‘[T]he plain language of the Act recognizes that
standards of performance leading to the ‘capture’ of
emissions are not infeasible [citation omitted], and
EPA has proposed to apply measurement
methodologies to flares in spite of the transience of
their emissions.’’
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commenter noted that 40 CFR part 60,
subpart Ja was promulgated as part of
the mandatory periodic review of 40
CFR part 60, subpart J required by CAA
section 111(b)(1)(B). The commenter
noted that subpart J exempts a flare from
the H2S concentration limits when
combusting certain gases generated
during SSM events (see 40 CFR
60.104(a)(1), 60.101(e)) and stated that
the record contains ‘‘ample evidence’’ to
support maintaining that provision in
subpart Ja. The commenter asserted that
including these same provisions in
subpart Ja is ‘‘an appropriate exercise of
EPA’s authority to ‘not review’ this
aspect of the existing standard in light
of the efficacy of the existing standard.’’
See CAA section 111(b)(1)(B).
Second, the commenter noted that the
Sierra Club decision was largely
grounded in the Court’s determination
that Congress amended CAA section 112
out of concern ‘‘about the slow pace of
EPA’s regulation of HAPs,’’ eliminating
much of the EPA’s discretion and
requiring sources to ‘‘meet the strictest
standards’’ without variance ‘‘based on
different time periods.’’ The commenter
further explained that the Court pointed
to CAA section 112(d)(1) regarding the
EPA’s authority to ‘‘distinguish among
classes, types, and sizes of sources’’
when promulgating CAA section 112
standards as further evidence for
constraining the EPA’s ability to adopt
different standards applicable during
SSM events. In contrast, the commenter
asserted that ‘‘Congress has expressed
no such concern about EPA’s efforts to
implement section 111’’ despite
revisions to CAA section 111 in 1977
and 1990. Therefore, the commenter
asserted, Congress has ‘‘effectively
ratified EPA’s longstanding approach to
SSM under the NSPS program,’’ which
includes the exemption for flares from
the H2S concentration limits during
SSM events.
The commenter also asserted that,
regardless of the above and despite the
similar nature of the provisions in CAA
sections 111 and 112, the EPA has the
discretion to implement them
differently ‘‘under the markedly
differently context of the NSPS program
v. the MACT program.’’ See
Environmental Defense v. Duke Energy
Corp., 549 U.S. 561, 575–576 (2007). For
example, the commenter asserted that
the word ‘‘continuous’’ as used in the
NSPS program could be interpreted and
applied differently, as acknowledged by
the Court in National Lime Ass’n v.
EPA, 627 F.2d 416, 434 (DC Cir. 1980)
(deferring to agency regarding the effect
of ‘‘the perplexing implications of
Congress’ new requirement of systems
of continuous emission reduction’’ on
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56441
the agency’s longstanding ‘‘regulations
permitting flexibility to account for
startups, shutdowns, and
malfunctions’’). The commenter urged
the EPA to exercise this discretion and
‘‘reassert the many practical, technical
and economic factors’’ that justify
promulgating separate standards for
SSM events in the NSPS program.
Third, the commenter asserted that
requiring flares to meet the H2S
concentration limits during SSM events
does not represent BSER for this time
period. According to the commenter,
‘‘startup and shutdown gases are
intermittent streams that cannot be cost
effectively treated for sulfur removal
because of their infrequent occurrence,
their scattered points of generation and
their variability.’’ Therefore, for all of
the above reasons, the commenter
asserted that exempting a flare from the
H2S concentration limits when
combusting certain gases generated
during SSM events is lawful under CAA
section 111.
Alternatively, the commenter stated
that if a standard must apply during
SSM events, the flare work practice
standards are appropriate in lieu of the
H2S concentration limit.
Response: Regardless of whether or
how the Sierra Club decision under
CAA section 112 applies to NSPS
promulgated under CAA section 111,
we are promulgating final amendments
for flares that include a suite of
standards that apply at all times and are
aimed at reducing SO2 emissions from
flares. As described previously, this
suite of standards requires refineries to:
(1) Develop and implement a flare
management plan; (2) conduct root
cause analysis and take corrective action
when waste gas sent to the flare exceeds
a flow rate of 500,000 scf above the
baseline; (3) conduct root cause analysis
and take corrective action when SO2
emissions exceed 500 lb in a 24-hour
period; and (4) optimize management of
the fuel gas by limiting the short-term
concentration of H2S to 162 ppmv
during normal operating conditions.
Additionally, refineries must install and
operate monitors for measuring sulfur
and flow at the inlet of all of their flares.
Together, these requirements provide
CAA section 111-compliant standards
that collectively cover all operating
conditions of the flare.
As the commenter notes, CAA section
111(h)(1) allows the EPA to promulgate
a design, equipment, work practice or
operational standard or ‘‘combination
thereof,’’ when ‘‘it is not feasible to
prescribe or enforce a standard of
performance’’ which reflects BSER for
the particular affected source. CAA
section 111(h)(2) defines the phrase
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
‘‘not feasible to prescribe or enforce a
standard of performance’’ as ‘‘any
situation in which the Administrator
determines that * * * a pollutant or
pollutants cannot be emitted through a
conveyance designed and constructed to
emit or capture such pollutant, or that
any requirement for, or use of, such a
conveyance would be inconsistent with
any Federal, State, or local law, or
* * * the application of measurement
methodology to a particular class of
sources is not practicable due to
technological or economic limitations.’’
We have determined that flares meet
the criteria set forth in CAA section
111(h)(2)(A) because emissions from a
flare do not occur ‘‘through a
conveyance designed and constructed to
emit or capture such pollutant.’’ Gases
are conveyed to the flare for destruction,
and combustion products such as SO2
are not created until combustion occurs,
which happens in the flame that burns
outside of the flare tip. In other words,
the SO2, NOX, PM, CO, VOC and other
pollutants generated from burning the
gases are only created once the gases
pass through the flare and come into
contact with the flame burning on the
outside of the flare. The flare itself is not
a ‘‘conveyance’’ that is ‘‘emitting’’ or
‘‘capturing’’ these pollutants; instead, it
is a structure designed to combust the
gases in the open air. Thus, setting a
standard of performance for SO2 (and
other pollutants) is not ‘‘feasible,’’
allowing the EPA to instead promulgate
standards under CAA section 111(h),
which will collectively limit emissions
from the flare.
The EPA previously promulgated a
standard of performance for SO2
emissions for fuel gas combustion
devices which also applied to flares. 39
FR 9308, 9315 (March 8, 1974). The
standard is expressed as an H2S
concentration limit because it was
developed as an alternative to
measuring the SO2 concentration in the
stack gases exiting fuel gas combustion
devices other than flares (i.e., boilers
and process heaters). That approach is
appropriate for fuel gas combustion
devices other than flares because
measuring the H2S in the fuel gas
combusted in those devices is directly
indicative of the SO2 emitted from the
exhaust stacks of those other devices. As
explained in section III of this preamble,
we are, for the first time, designating
flares as their own affected facility. As
such, in finalizing these amendments
for flares, we considered whether we
could also apply a standard of
performance for SO2 emissions,
expressed as an H2S concentration limit
or a total sulfur limit at the inlet to the
flare. However, as explained above,
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flares are substantially different from
other fuel gas combustion devices so
that this approach is not workable for
flares. For example, SO2 emissions from
a flare are dependent on many factors,
including the flow rates of all gases sent
to the flare, the total sulfur content of all
gases sent to the flare and the
combustion efficiency at the flare. Each
of these factors is also dependent on
many variables. For example,
combustion efficiency at the flare is
dependent upon the flammability of the
gases entering the flare, the turbulence
at the flare,9 the wind speed and wind
direction and the presence of other
pollutants in the gases that can react
with the sulfur to form sulfur-containing
pollutants other than SO2. Since so
many factors affect the potential
formation of SO2 emissions outside the
flare tip, we realized that we could not
properly derive an H2S concentration
limit or a total sulfur limit at the flare
inlet that would directly correlate with
those SO2 emissions. Thus, we
determined that we cannot set a
standard of performance for SO2
emissions at the flare.
However, we still recognize that
reducing the amount of sulfur that is
sent to a flare will reduce the SO2
emissions at the flare. Even with the
uncertainty described above, we
understand the importance of refineries
managing the fuel gas sent to their flares
in a way that minimizes the sulfur
content so as to ultimately minimize the
SO2 emissions. Rather than eliminate
the H2S concentration limit altogether,
we are instead requiring under CAA
section 111(h) that refineries limit the
short-term concentration of H2S to 162
ppmv in the fuel gas sent to flares
during normal operating conditions.
Refineries rely on various methods for
optimizing the management of fuel gas,
including the use of amine treatment
and flare gas recovery systems. Amine
treatment removes the H2S from the
flare gas that generates the pollutants
before the gas is sent to the flare. Flare
gas recovery systems remove the flare
gas altogether and instead treat this gas
in a fuel gas treatment system to be used
elsewhere as fuel gas in the refinery.
Requiring refineries to meet this
concentration limit at the flare ensures
that the fuel gas has been adequately
treated and managed such that it can be
used as fuel gas in the fuel gas system
elsewhere in the refinery. We are not
requiring refineries to meet this limit
during other periods of operation
because flare gas recovery systems that
9 Turbulence is needed to insure good mixing at
the flare, but is affected by whether the flare is
assisted with air or steam or non-assisted.
PO 00000
Frm 00022
Fmt 4701
Sfmt 4700
capture gases prior to amine treatment
can be quickly overwhelmed and fail to
properly function during high fuel gas
flows. Thus, requiring that flares meet
this H2S concentration limit during
periods when high fuel gas flows would
likely overwhelm these flare gas
recovery systems would not fully
address the circumstances refineries
face in managing these high flow
periods. Designing flare gas recovery
systems to capture the full range of gas
flows to the flare would not only require
the ability to predict the full range of gas
flows in the flare headers, but also
would require refiners to install
recovery compressors in a staged
fashion such that all events causing high
gas flows could be captured and
managed, neither of which are practical.
Therefore, promulgating flare
requirements that include the H2S fuel
gas concentration limit during normal
operating conditions, coupled with
requirements for refineries to develop
and implement a flare management plan
and conduct root cause analyses and
take corrective action when waste gas
sent to the flare exceeds a flow rate of
500,000 scf above the baseline or 500 lb
of SO2 in a 24-hour period, recognizes
these unique circumstances while still
requiring the refinery to take all
reasonable measures for reducing or
eliminating the flow and sulfur content
of gases being sent to the flares.
We are aware that numeric SO2
emission limits for flares have been
established under state law and in
Federal Implementation Plan (FIP)
regulatory requirements. Those sourcespecific circumstances differ markedly
from this nationally applicable
rulemaking, necessitating different
decisions in two very different
circumstances. For example, the EPA’s
SO2 FIP for the Billings/Laurel, Montana
area includes a SO2 emission limit of
150 lb of SO2 per 3 hours for four
sources that apply to the flares at all
times. See 40 CFR 52.1392(d)(2)(i),
(e)(2)(i), (f)(2)(i) and (g)(2)(i). These
source-specific limits were
appropriately based on dispersion
modeling in the Billings/Laurel area to
determine what was needed to meet
national ambient air quality standards
(NAAQS) for SO2 in the Billings/Laurel
area. In contrast, the nationally
applicable standards and requirements
we are promulgating in this rule must
represent the BSER achievable for an
entire industry sector scattered across
the entire country. This requires that we
consider costs and other non-air quality
factors that affect all petroleum
refineries nationwide in making that
decision and not just as applied to a
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particular group of sources in a
particular location.
Additionally, those four sources
subject to the Billings/Laurel FIP
demonstrate compliance with the 150 lb
SO2/3-hour emission limit by measuring
the total sulfur concentration and
volumetric flow rate of the gas stream at
the inlet to the flare. See 40 CFR
52.1392(d)(2)(ii), (e)(2)(ii), (f)(2)(ii),
(g)(2)(ii) and (h). Since the FIP must
include emissions limits that insure
attainment and maintenance of the
NAAQS in the Billings/Laurel area, it
was appropriate, in setting the standards
for the Billings/Laurel FIP, to
conservatively assume that 100 percent
of the sulfur in the gases discharged to
the flare is converted to SO2, and based
on this conversion, set the numeric limit
as a value that is not to be exceeded.
However, that same assumption is not
appropriate when setting national
standards for flares. Instead, we must
consider the many factors affecting the
formation of SO2 at the flare tip and
how these factors affect how much of
the sulfur in the gases sent into the flare
actually converts to SO2. Therefore,
although setting such source-specific
limits was appropriate to satisfy what
the modeling showed was necessary to
meet the SO2 NAAQS in the Billings/
Laurel area, a different analysis and
standard is appropriate for a national
rulemaking.
Therefore, for the reasons discussed
above, the EPA is finalizing this
collective set of CAA section 111(h)compliant standards for flares, based on
our interpretation of CAA section 111(h)
as it applies to flares.
Comment: Numerous commenters
asserted that the long-term 60 ppmv H2S
fuel gas concentration limit is not cost
effective for flares and, therefore, not
BSER for flares. The commenters noted
that the EPA did not include costs for
compressors, additional amine units
and sulfur recovery units, and one
commenter stated that the EPA did not
consider the range of costs that are
incurred by individual refineries.
Commenters also asserted that the EPA
overstated emission reductions by using
162 ppmv H2S as a baseline because
many refinery streams currently sent to
the flare contain H2S concentrations
below 162 ppmv, so 162 ppmv H2S does
not reflect long-term performance.
Commenters noted that the British
thermal units (Btu) content of flare gas
is highly variable and generally lower
than that used by the EPA, so the EPA’s
analysis overestimated the value of the
recovered flare gas. One commenter
noted that the EPA should have
considered consent decree requirements
in the baseline SO2 emissions estimates.
One commenter stated that the longterm 60 ppmv H2S fuel gas
concentration limit could preclude
some refineries from processing highsulfur crude oils, thereby limiting
refining production capacity. Another
commenter noted that many flares will
receive both fuel gas and process upset
gas, so it would be impossible to
determine if an exceedance is caused by
the regulated fuel gas or by the exempt
gas. The commenter recommended that
the EPA apply the long-term 60 ppmv
H2S fuel gas concentration limit only to
fuel gas combusted in process heaters,
boilers and similar fuel gas combustion
devices, and not to flares, or that the
EPA allow Alternative Monitoring Plans
to demonstrate compliance with the
emissions limits for non-exempt gas
streams upstream of the flare header.
Response: We acknowledge that, at
proposal, we determined that a longterm 60 ppmv H2S fuel gas
concentration limit was cost effective
primarily for process heaters, boilers
and other fuel gas combustion devices
that are fed by the refinery’s fuel gas
system. Based on the typical
configuration at a refinery, adding one
new fuel gas combustion device to the
fuel gas system would essentially
require the owner or operator to limit
the long-term concentration of H2S in
the entire fuel gas system to 60 ppmv,
so emission reductions would result
from all fuel gas combustion devices
tied to that fuel gas system. Upon
review of the BSER analysis conducted
at proposal for fuel gas combustion
devices, we now realize that the
analysis is not applicable to flares (See
Docket Item No. EPA–HQ–OAR–2007–
0011–0289).
Moreover, since we are regulating
flares separately from other fuel gas
combustion devices in this final rule,
56443
we should separately consider whether
a long-term H2S concentration limit is
appropriate for fuel gas sent to flares.
In developing the suite of CAA
section 111(h) standards for flares, we
considered whether refineries should be
required to optimize management of
their fuel gas by limiting the long-term
H2S concentration to 60 ppmv in
addition to the short-term H2S
concentration of 162 ppmv during
normal operating conditions. We
determined that, for refineries to
demonstrate that their fuel gas complies
with a long-term H2S concentration of
60 ppmv, refineries would have to
install a flare gas recovery system
(which was not needed for other fuel gas
combustion devices) and then upgrade
the fuel gas desulfurization system.
Alternatively, refineries would have to
treat the recovered fuel gas to limit the
long-term concentration of H2S to 60
ppmv with new amine treatment units
on each flare.
While some of the costs provided by
the commenters did not include the
value of the recovered gas and appeared,
at times, to include equipment not
necessarily required by the regulation,
we generally agree with the
commenters, based on our own cost
estimates, that optimizing management
of the fuel gas system to limit the longterm concentration of H2S to 60 ppmv
is not cost effective for flares (see Table
4 below). We note that the costs
provided by the commenters and the
costs and emissions reductions in our
analysis are the incremental costs and
emissions reductions of going from the
short-term 162 ppmv H2S concentration
to a combined short-term 162 ppmv H2S
concentration and long-term 60 ppmv
H2S concentration. While we are aware
that some consent decrees require
refineries to limit the concentration of
H2S in the fuel gas to levels lower than
the short-term 162 ppmv H2S
concentration, our baseline when
evaluating the impacts of a national
standard (in this case, 40 CFR part 60,
subpart Ja) is the national set of
requirements to which an affected flare
would be subject in the absence of
subpart Ja (i.e., the short-term 162 ppmv
H2S concentration limit in 40 CFR part
60, subpart J).
TABLE 4—NATIONAL FIFTH YEAR IMPACTS OF MEETING A LONG-TERM 60 PPMV H2S CONCENTRATION FOR FLARES
SUBJECT TO 40 CFR PART 60, SUBPART JA
Capital cost
($1,000)
New ..........................................................
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Total annual
cost
($1,000/yr) a
80,000
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Emission
reduction
(tons SO2/yr) b
Emission
reduction
(tons NOX/yr) b
6
34
15,000
Fmt 4701
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Emission
reduction
(tons VOC/
yr) b
130
Cost
effectiveness
($/ton)
84,000
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
TABLE 4—NATIONAL FIFTH YEAR IMPACTS OF MEETING A LONG-TERM 60 PPMV H2S CONCENTRATION FOR FLARES
SUBJECT TO 40 CFR PART 60, SUBPART JA—Continued
Capital cost
($1,000)
Modified/Reconstructed ...........................
Total annual
cost
($1,000/yr) a
860,000
Emission
reduction
(tons SO2/yr) b
Emission
reduction
(tons NOX/yr) b
53
310
160,000
Emission
reduction
(tons VOC/
yr) b
1,200
Cost
effectiveness
($/ton)
100,000
a Because
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of the heat content of recovered gas, each scf of recovered gas is assumed to offset one scf of natural gas; a value of $5/10,000
scf of natural gas was used to estimate recovery credit.
b These emission reductions are based on flares already meeting the short-term 162 ppmv H S fuel gas concentration limit in 40 CFR part 60,
2
subpart J (i.e., these are the incremental emission reductions achieved from a baseline of optimizing management of the fuel gas system to limit
the short-term H2S concentration in the fuel gas to 162 ppmv to the originally proposed combined short-term 162 ppmv H2S concentration and
long-term 60 ppmv H2S concentration in the fuel gas).
Comment: Several commenters
addressed the EPA’s request for
comment on ‘‘the equivalency of the
subpart Ja requirements as proposed to
be amended today and the SCAQMD
Rule 1118’’ and ‘‘whether EPA could
deem a facility in compliance with
subpart Ja as proposed to be amended
today if that facility was found to be in
compliance with SCAQMD Rule 1118,
or other equivalent State or local rules’’
(73 FR 78532, December 22, 2008). One
commenter disagreed with the EPA’s
position, alleging that ‘‘EPA’s suggestion
that it can waive compliance with the
NSPS in this manner is contrary to the
Clean Air Act.’’ The commenter stated
that the EPA’s suggestion ‘‘that existing
state and local requirements render the
federal requirements irrelevant only
confirms that EPA’s proposed flaring
requirements do not reflect the best
technological system of continuous
emission reduction.’’ 42 U.S.C.
7411(h)(1) (emphasis added). The
commenter also stated that the CAA
already provides a mechanism for
implementation of alternative work
practice standards in narrowly defined
circumstances (42 U.S.C. 7411(h)(3)); an
owner or operator may demonstrate to
the Administrator that an alternative
means of emissions limitation is
equivalent to the federal standard on a
case-by-case basis. Therefore, the
commenter asserted, the CAA clearly
states that ‘‘EPA’s authority to waive
federal work practice standards is case
specific.’’ Finally, the commenter stated
that the EPA did not explain how
emissions reductions achieved through
compliance with SCAQMD Rule 1118
are equivalent to 40 CFR part 60,
subpart Ja. Further, the commenter
asserted that the EPA neither identified
other state or local rules that could be
considered equivalent to subpart Ja, nor
explained how the EPA would
determine that a specific state or local
rule is equivalent to subpart Ja.
Therefore, the commenter asserted, it is
impossible to fully assess the merit of
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the EPA’s idea and provide meaningful
comments.
Another commenter stated that ‘‘most
stringent’’ is not one of the criteria that
must be applied under the law to
determine BSER. Therefore, the
commenter asserted, it is not
appropriate to argue that the EPA did
not properly determine BSER simply
because there exist state or local rules
that are more stringent than federal
requirements. The commenter also
asserted that the EPA has full authority
to establish alternative regulatory
standards that are determined to be as
stringent as or more stringent than
BSER, and CAA section 111(h)(3)
generally applies after the EPA has
completed a national rulemaking and an
owner or operator requests approval for
a site-specific alternative at a later date.
The commenter asserted that it is logical
that, if an alternative method is
identified during the rulemaking
process, ‘‘the law would allow EPA to
establish a site-specific alternative [in
the rule itself] (especially, as under
[CAA section 111], where the alternative
would have to be determined through
notice and comment rulemaking).’’
Other commenters recommended that
refineries complying with SCAQMD
Rule 1118 be deemed in compliance
with 40 CFR part 60, subparts J and Ja.
According to one commenter, SCAQMD
Rule 1118 is ‘‘in all respects equivalent
to or more stringent than the
corresponding requirements’’ of
subparts J and Ja. Commenters also
recommended that refineries should be
able to consider compliance with
BAAQMD Regulation 12, Rule 11 and
Regulation 12, Rule 12 as compliance
with the appropriate provisions of
subpart Ja. One commenter provided a
table comparing each of the six
proposed flare management plan
requirements in 40 CFR 60.103a(a) to
the SCAQMD and BAAQMD
regulations. The table identified
sections of BAAQMD Regulation 12,
Rule 11 and Regulation 12, Rule 12 that
are equivalent to the six subpart Ja flare
PO 00000
Frm 00024
Fmt 4701
Sfmt 4700
management plan requirements. The
commenter also noted that SCAQMD
Rule 1118 is only equivalent to five of
the proposed requirements; it does not
require an owner or operator to identify
procedures to reduce flaring in cases of
fuel gas imbalance (although another
commenter noted that SCAQMD Rule
1118 requires minimization of all
flaring, including fuel gas imbalance).
While most commenters focused on the
equivalence of the flare management
plan requirements of the SCAQMD and
BAAQMD rules and the flare
management plan requirements of
subpart Ja, one commenter requested
that the periodic sampling of BAAQMD
Regulation 12, Rule 11 be considered
equivalent to the continuous sulfur
monitoring requirements of subpart Ja
for emergency flares.
Response: First, we note that there
seems to be some misunderstanding
regarding how a determination that
SCAQMD Rule 1118 or BAAQMD
Regulation 12, Rule 11 and Regulation
12, Rule 12 are equivalent to 40 CFR
part 60, subpart Ja would actually be
implemented in subpart Ja. The EPA
will not ‘‘waive’’ the obligation to
comply with subpart Ja if the source is
complying with SCAQMD Rule 1118 or
BAAQMD Regulation 12, Rule 11 and
Regulation 12, Rule 12. In other words,
the EPA will not allow the owner or
operator to ‘‘choose’’ to comply with
SCAQMD Rule 1118 or BAAQMD
Regulation 12, Rule 11 and Regulation
12, Rule 12 instead of subpart Ja. Rather,
the source must always demonstrate
compliance with subpart Ja. If SCAQMD
Rule 1118 or BAAQMD Regulation 12,
Rule 11 and Regulation 12, Rule 12 are
determined to be equivalent to subpart
Ja, then these requirements would be
provided as an alternative within
subpart Ja for the source to demonstrate
that it is meeting the requirements of
subpart Ja.
To assess the comments, we reviewed
SCAQMD Rule 1118, BAAQMD
Regulation 12, Rule 11, and BAAQMD
Regulation 12, Rule 12 and compared
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these rules to the 40 CFR part 60,
subpart Ja requirements we are
finalizing here. We have included
documentation of this review in Docket
ID No. EPA–HQ–OAR–2007–0011 that
shows the sections of each of those rules
that we consider are equivalent to the
subpart Ja requirements. We determined
that SCAQMD Rule 1118 and BAAQMD
Regulation 12, Rule 11 and Regulation
12, Rule 12 will result in equivalent to
or greater than the emissions reductions
resulting from the subpart Ja flare
management plan requirements. As a
result of our analysis, we have amended
subpart Ja, as described in the following
paragraphs.
We determined that SCAQMD Rule
1118 is equivalent to the flare
requirements and monitoring,
recordkeeping and reporting provisions
for determining compliance with the
flare requirements in 40 CFR part 60,
subpart Ja. We also determined that the
combined provisions of BAAQMD
Regulation 12, Rule 11 and BAAQMD
Regulation 12, Rule 12 are equivalent to
the flare requirements and monitoring,
recordkeeping and reporting provisions
for determining compliance with the
flare requirements in subpart Ja.
Therefore, we have added specific
compliance options for flares that are
located in the SCAQMD and are in
compliance with SCAQMD Rule 1118,
as well as for flares that are located in
the BAAQMD and are in compliance
with both BAAQMD Regulation 12, Rule
11 and BAAQMD Regulation 12, Rule
12. Flares that are in compliance with
these alternative compliance options are
in compliance with the flare standards
in subpart Ja. Specifically, 40 CFR
60.103a(g) specifies that flares that are
located in the SCAQMD may elect to
comply with SCAQMD Rule 1118 and
flares that are located in the BAAQMD
may elect to comply with both
BAAQMD Regulation 12, Rule 11 and
BAAQMD Regulation 12, Rule 12 to
comply with the flare management plan
requirements of 40 CFR 60.103a(a) and
(b) and the root cause analysis and
corrective action analysis requirements
of 40 CFR 60.103a(c) through (e). In
addition, 40 CFR 60.107a(h) indicates
that flares that are located in the
SCAQMD may elect to comply with the
monitoring requirements of SCAQMD
Rule 1118 and flares that are located in
the BAAQMD may elect to comply with
the combined monitoring requirements
of both BAAQMD Regulation 12, Rule
11 and BAAQMD Regulation 12, Rule
12 to comply with the monitoring
requirements of 40 CFR 60.107a(e) and
(f). The owner or operator must notify
the Administrator, as specified in 40
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20:34 Sep 11, 2012
Jkt 226001
CFR 60.103a(g), that the flare is in
compliance with SCAQMD Rule 1118 or
both BAAQMD Regulation 12, Rule 11
and BAAQMD Regulation 12, Rule 12.
The owner or operator must also submit
a copy of the existing flare management
plan (if applicable), as specified in 40
CFR 60.103a(g).
We note that, as pointed out by
commenters, an owner or operator
maintains the ability under CAA section
111(h)(3) to submit a request to
establish, on a case-by-case basis, that
‘‘an alternative means of emission
limitation will achieve a reduction in
emissions * * * at least equivalent to
the reduction in emissions’’ achieved
under the flare standards of 40 CFR part
60, subpart Ja. Pursuant to CAA section
111(h)(3), we also included specific
provisions within 40 CFR 60.103a for
owners or operators to submit a request
for ‘‘an alternative means of emission
limitation’’ that will achieve a reduction
in emissions at least equivalent to the
reduction in emissions achieved under
the final standards in subpart Ja.
Comment: Commenters suggested that
the requirement to minimize discharges
to the flare in 40 CFR 60.103a(a)(1)
should specifically address routine
discharges, and the EPA should limit
the minimization requirements to
actions that: (1) Are ‘‘consistent with
good engineering practices’’ and (2)
consider costs and other health and
environmental impacts, as required by
section 111 of the CAA.
Response: We agree that the language
in proposed 40 CFR 60.103a(a)(1)
appears to require an assessment of flare
minimization irrespective of cost or
other relevant considerations, as
contained in CAA section 111, which
was not our intent. We are clarifying,
through this response, that cost, safety
and emissions reductions may be
considered when evaluating what
actions should be taken to minimize
discharges to a flare, but we disagree
that the flare minimization assessment
should be limited to ‘‘routine
discharges.’’ We have revised the flare
management plan requirements in 40
CFR 60.103a(a) to more fully describe
the types of information that must be
evaluated and included in the plan.
As noted in the summary of this rule
(section III.C of this preamble), we are
finalizing our proposed withdrawal of
the 250,000 scfd 30-day rolling average
flow limit for flares. This limitation
does not adequately account for sitespecific factors regarding flare gas Btu
content, ability to offset natural gas
purchase and other considerations. We
find that these factors need to be
addressed in a site-specific basis and are
more appropriately addressed through
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the flare management plan. In the
absence of the specific flow limitation,
we have included additional
requirements in the flare management
plan to prompt a thorough review of the
flare system so that, as an example, flare
gas recovery systems are installed and
used where these systems are
warranted. We have also revised the
flare minimization requirements to
require the flare management plans to
be submitted to the Administrator (40
CFR 60.103a(b)).
As part of the development of the
flare management plan, refinery owners
and operators can provide rationale and
supporting evidence regarding the flare
reduction options considered, the costs
of each option, the quantity of flare gas
that would be recovered or prevented by
the option, the Btu content of the flare
gas and the ability or inability of the
reduction option to offset natural gas
purchases. The plan will also include
the rationale for the selected reduction
option, including consideration of safety
concerns. The owner or operator must
comply with the plan, as submitted to
the Administrator. Major revisions to
the plan, such as the addition of an
alternative baseline (see next comment
for further detail on baselines), must
also be submitted to the Administrator.
In summary, although we did not
incorporate the commenter’s suggested
language for limiting the scope of the
minimization requirements to actions
that are ‘‘consistent with good
engineering practices’’ and that
‘‘consider costs and other health and
environmental impacts,’’ we
acknowledge that these are valid
considerations in the selection of the
minimization alternatives available for a
given affected flare. We find that the
process of developing and submitting
the flare management plan will ensure
that these factors are considered
consistent with CAA section 111 and
that the requirement to minimize
discharges to the flare is implemented
consistently across all affected sources.
Comment: Commenters asserted that
the flare flow root cause analysis
threshold of 500,000 scf in any 24-hour
period is arbitrary and cannot be fairly
applied to all flares at all refineries. One
commenter cited an ultracracker flare
that routinely cycles from 5 million to
25 million scfd as an example of a flare
for which the threshold of 500,000 scf
in any 24-hour period would result in
constant and meaningless root cause
analyses. The commenters suggested
removing the numerical threshold and
limiting root cause analysis to upsets
and malfunctions as initially
promulgated in June 2008 (because root
cause analysis is generally only effective
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for reducing non-routine flows) or using
a site- or flare-specific threshold
instead. Even if the numerical threshold
is revised, the commenters suggested
that a number of streams be excluded
from the calculation of flow, such as
hydrogen and nitrogen, purge and
sweep gas, natural gas added to increase
the Btu content of the flare gas and gases
regulated by other rules to avoid
performing multiple root cause analyses
for routine events. One commenter
suggested that owners or operators
should be able to use one root cause
analysis report for an event that occurs
routinely (as allowed in the consent
decrees).
Response: We proposed the flare flow
root cause analysis threshold of 500,000
scf in any 24-hour period because we
projected that flare gas recovery would
be a cost effective emission reduction
technique for flares with fuel gas flows
that routinely exceed 500,000 scfd,
although we acknowledge that the
threshold at which flare gas recovery
becomes cost effective is strongly
(inversely) correlated to the average Btu
content of the flare gas (i.e., a relatively
small reduction in the Btu content of the
gas makes the recovery system
significantly less cost effective).
Although we did not specifically
exclude sweep or purge gas from the
flow, we expected that the flow rates of
sweep or purge gas (i.e., gases needed to
ensure the readiness of the flare and the
safety of the flare gas system) would be
negligible when compared to the root
cause analysis threshold of 500,000 scf
in any 24-hour period. In fact, in our
original analysis of the appropriate flow
rate root cause analysis threshold
(Docket Item No. EPA–HQ–OAR–2007–
0011–0246), we essentially assumed
that the sweep and purge gas flow rates
were zero, and we estimated costs and
emissions reductions of the 500,000 scf
in any 24-hour period threshold, based
on recovering that amount of gas or
eliminating recurring events of that size
(rather than 500,000 scf minus the
sweep or purge gas flow).
However, while we do not believe
that 5 million scfd 10 is a reasonable
10 Regarding commenter’s cited ultracracker flare
example, it is difficult to believe that sweep gas
alone accounts for 5 million scfd of flare gas flow.
Additionally, a compositional analysis of the base
flare gas from the normal flow, based on data
provided from a DIAL study of this refinery,
suggests that the base flare gas is of sufficient
quality to recover. It also appears, based on the data
provided by the commenter, that the hydrogen
stream recycle compressor was off-line
approximately half the year. For such huge gas
flows, considering the cost of purchasing or
producing additional hydrogen and the emissions
associated with that process, it is reasonable to
expect that the facility would have a back-up
compressor if the primary compressor is unreliable.
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base flow for a flare, we do acknowledge
that the size of the flare, as well as the
flare header system, will greatly impact
the required flow needed to maintain
the readiness of the flare. Although we
can derive suitable flare flow thresholds
for average conditions, these thresholds
are not necessarily reasonable when
applied to all flows, and we did not
intend for on-going root cause analyses
to be conducted on account of sweep or
purge gas.
Therefore, rather than specifying a
one-size-fits-all threshold, the final rule
requires facilities to develop their own
base flare flow rates as part of their flare
management plan. A flow-based root
cause analysis is triggered if flows
measured by the flow monitor exceed
500,000 scf greater than the base flare
flow rate in any 24-hour period.
Evaluating the flow rate threshold above
a baseline better reflects our original
analysis of the impacts of flow-based
root cause analyses when the sweep or
purge gas flow rates are not negligible.
We also note that 40 CFR 60.103a(d)
allows a single root cause analysis to be
conducted for any single continuous
discharge that causes the flare to exceed
either the root cause analysis threshold
for SO2 or flow for two or more
consecutive 24-hour periods.
The final rule does not limit root
cause analyses to upsets and
malfunctions of refinery process units
and ancillary equipment connected to
the flare, nor does it explicitly allow
owners or operators to use one root
cause analysis report for an event that
occurs routinely. When we decided to
eliminate the numerical limit on flare
flow rate, we specifically increased the
scope of the flare flow root cause
analysis to cover more than just upsets
and malfunctions. We also decided not
to explicitly allow owners or operators
to use one root cause analysis report for
an event that occurs routinely as a
means to discourage routine flaring of
recoverable gas. However, we recognize
that there may be recurring discharges
to the flare that are not recoverable for
various reasons. Therefore, the final rule
does allow for several base cases, which
could include recurring maintenance;
this provision will avoid multiple root
cause analyses for a recurring event. As
described above, the flare management
plan (as well as significant revisions to
the plan to include alternative
baselines) must be submitted to the
Administrator. The Administrator or
delegated authority (e.g., the state) may
review the plan, although formal
approval of the plan is not required. Not
specifying a formal approval process is
intended to minimize the burden
associated with reviewing flare
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management plans. Rather, the rule
specifies elements of the plan that need
to be addressed in order for the plan to
be considered adequate and provides an
opportunity for a delegated authority to
find the plan not adequate if they
choose to do so.
We expect that a final flare
management plan in compliance with
40 CFR part 60, subpart Ja will possess
the following characteristics: (1)
Completeness (all gas streams are
considered, all required elements are
included and all appropriate flare
reduction measures are evaluated); (2)
accuracy (the emission reductions and
cost estimates for the different options
are accurate); and (3) reasonableness
(the selection of reduction options is
correct and the baseline flow value is
reasonable). If the Administrator
identifies deficiencies in the plan (e.g.,
the plan does not contain all the
required elements, alternative flare
reduction options were not evaluated or
selected when reasonable, the baseline
or alternative baseline flow rates are
considered unreasonable), the
Administrator will notify the owner or
operator of the apparent deficiencies.
The owner or operator must either
revise the plan to address the
deficiencies or provide additional
information to document the
reasonableness of the plan.
Comment: Commenters requested
alternative monitoring options or an
exemption from continuous flow
monitoring for: (1) Flares designed to
handle less than 500,000 scfd of gas; (2)
pilot gas; (3) flares with flare gas
recovery systems; (4) emergency flares;
and (5) secondary flares. The
commenters asserted that flow meters
are costly and engineering calculations,
which are currently used, are sufficient
to evaluate when the flow to a flare
exceeds 500,000 scf in any 24-hour
period. One commenter stated that, for
flares with flare gas recovery systems,
the pressure drop across the flare seal
drum can be used to calculate flow rate.
Response: In the final rule, flow
monitoring is used to determine
whether a root cause analysis is
required rather than to ensure
compliance with a specific flow limit.
We have reviewed the commenters’
suggestions and agree that, in certain
specific cases, monitoring is not
necessary and should not be required.
However, as a general rule, we believe
flow monitors are needed, not only to
provide a verifiable measure of
exceedances of the flow root cause
analysis threshold, but also exceedances
of the root cause analysis threshold of
500 lb SO2 in any 24-hour period. In
addition, when we evaluated local rules,
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such as the initial BAAQMD rule for
flare monitoring, we saw that the
measured flare flow rates were several
times greater than previously projected
by the facilities.
Consequently, we find great value in
the flow monitoring requirements for
flares. These monitoring requirements
will greatly improve the accuracy of
emissions estimates from these flares.
The resulting improved accuracy of flare
emissions estimates will also lead to
better decision-making as we conduct
future reviews of rules applicable to
petroleum refineries. We did consider
each of the commenters’ suggested
exemptions in light of this fact; our
specific considerations follow.
We did not specifically consider that
some flares would not be capable of
exceeding the flow root cause analysis
threshold (i.e., designed to handle less
than 500,000 scfd of gas). However,
these small flares could still exceed the
root cause analysis threshold of 500 lb
SO2 in any 24-hour period. As such, we
did not provide an exemption from the
monitoring requirements for these small
flares.
We agree that the monitoring of pilot
gas flow is not needed. In the final rule,
a root cause analysis is required if the
gas flow to the flare exceeds 500,000 scf
above the baseline in any 24-hour
period. The flow of pilot gas is
considered to be part of the baseline
flow and is assumed to be constant. As
such, monitoring of pilot gas would not
be necessary to determine whether a
flare has exceeded 500,000 scf above the
baseline in any 24-hour period. In
practice, the actual baseline flow set for
the flare may or may not expressly
include the pilot gas flow rate.
Generally, the configuration of the flare
header is such that the flare flow
monitor would not measure pilot gas
flow. In this case, the baseline flow
determined for the flare would not
expressly include the pilot gas flow rate.
If the flare flow monitor is configured in
such a way that it does measure pilot
gas, then pilot gas would be considered
part of the baseline conditions for that
flare.
We agree with commenters that flares
with flare gas recovery systems do have
unique conditions and these warrant
alternative monitoring options.
Additionally, we recognize that the
monitoring requirements may be
burdensome for flares that are truly
‘‘emergency only’’ (i.e., flares that flare
gas rarely, if at all, during a typical year)
or for secondary flares in a cascaded
flare system. These flares are expected
to have a water seal that prevents flare
use during normal operations and
ensures that the pressure upstream of
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the water seal (expressed in inches of
water) does not exceed the water seal
height during normal operations
(hereafter referred to as ‘‘properly
maintain a water seal’’). We find that,
for these select types of flares, water seal
monitoring as an alternative to the flow
(and sulfur) monitoring provisions is
appropriate.
For flares with a flare gas recovery
system and other emergency or
secondary flares that properly maintain
a water seal, the final rule states that an
owner or operator may elect to monitor
the pressure in the gas header just
before the water seal and monitor the
water seal liquid height to verify that
the flare header pressure is less than the
water seal, which is an indication that
no flow of gas occurs. If the flare header
pressure exceeds the water seal liquid
level, a root cause analysis is triggered
unless the pressure exceedance is
attributable to staging of compressors.
This alternative reduces the costs
associated with installing sulfur and
flow monitoring systems for flares that
rarely receive fuel gas. Engineering
calculations can be used to estimate the
emissions during the event, but not for
determining whether or not a root cause
analysis is required.
To ensure that this option is only
used for flares that are truly emergency
flares and not for flares that are used for
routine discharges, the final rule
contains a limit on the number of
pressure exceedances requiring root
cause analyses that can occur in one
year. Following the fifth reportable
pressure exceedance in any consecutive
365 days, the owner or operator must
comply with the sulfur and flow
monitoring requirements of 40 CFR
60.107a(e) and (f). Based on a review of
available flaring data, we expect that gas
may be sent to an emergency flare three
to four times per year, on average.
Consistent with this information, we are
providing in these final amendments
that an ‘‘emergency flare’’ may receive
up to four releases to the flare in any
consecutive 365-day period to account
for year-to-year variability. However, a
flare receiving more than four
discharges in a consecutive 365-day
period can no longer be considered an
‘‘emergency flare’’ and must install the
required sulfur and flow monitors.
Comment: Commenters requested an
exemption from continuous sulfur
monitoring or alternative monitoring
options for flares handling only gases
inherently low in sulfur content,
emergency flares, flares with properly
designed flare gas recovery systems and
secondary flares. For flares handling
gases low in sulfur, the commenters
noted that continuous monitoring is
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56447
unnecessary and certain fuel gas streams
are already exempted from monitoring if
they are combusted in a fuel gas
combustion device. For flares that
handle only gases exempt from the H2S
concentration requirements and flares
with properly designed flare gas
recovery systems, commenters stated
that engineering calculations are
sufficient to determine if the SO2 root
cause analysis threshold of 500 lb in any
24-hour period is exceeded. One
commenter requested that the EPA
allow owners or operators to submit and
use an alternative monitoring plan to
demonstrate that the flare gas recovery
system is operating within its capacity
and to calculate SO2 emissions from
engineering calculations and flare gas
sampling. For secondary flares, one
commenter noted that the continuous
sulfur monitor on the primary flare
could be used to determine the sulfur
content of the gas being flared from the
secondary flare.
One commenter requested that the
EPA allow the use of engineering
calculations to determine the sulfur-toH2S ratio because sampling can be
difficult for emergency flares. One
commenter noted that the EPA should
allow the use of an existing continuous
monitoring system if the gas sent to the
flare is already monitored elsewhere. As
examples, the commenter cited fuel gas
and pilot gas already monitored within
the fuel gas system.
For flares that rarely see flow,
commenters particularly cited
difficulties with performance tests.
Commenters noted that, to meet the
sulfur monitor performance test
requirements, an owner or operator may
have to intentionally flare gas that may
not meet the H2S concentration limits.
One commenter also stated that
performing the required relative
accuracy test audit (RATA) could cause
the flare to exceed the root cause
analysis threshold. The commenter
recommended revising the performance
test requirements for flares with flare
gas recovery to require only a cylinder
gas audit.
Response: We have amended the final
rule so that gases that are exempt from
H2S monitoring due to low sulfur
content are also exempt from sulfur
monitoring requirements for flares. For
low-sulfur gases, the flare root cause
analysis will always be triggered by an
exceedance of the flow rate threshold
well before the SO2 threshold is
exceeded, so no sulfur monitoring is
required. However, this exemption can
only be used for flares that are
configured to receive only fuel gas
streams that are inherently low in sulfur
content, as described in 40 CFR
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60.107a(a)(3), such as flares used for
pressure relief of propane or butane
product spheres (fuel gas streams
meeting commercial grade product
specifications for sulfur content of 30
ppmv or less) or flares used to combust
fuel gas streams produced in process
units that are intolerant to sulfur
contamination (e.g., hydrogen plant,
catalytic reforming unit, isomerization
unit or hydrogen fluoride alkylation
unit). We already clarified that flare
pilot gas is not required to be
monitored. Also, 40 CFR part 60,
subpart Ja already allows for H2S
monitoring at a central location, such as
the fuel mix drum, for all fuel gas
combustion devices (and we are
finalizing amendments to ensure it is
clear that H2S monitoring at a central
location is allowed for flares as well).
Thus, we agree that if a flare only burns
natural gas, fuel gas monitored
elsewhere or fuel gas streams that are
inherently low in sulfur content (as
defined in 40 CFR 60.107a(a)(3)), then
no H2S monitor is needed.
The remaining issue is whether or not
sulfur monitoring is necessary for
‘‘emergency only’’ flares. (An emergency
flare is defined as a flare that combusts
gas exclusively released as a result of
malfunctions (and not startup,
shutdown, routine operations or any
other cause) on four or fewer occasions
in a rolling 365-day period. For
purposes of the rule, a flare cannot be
categorized as an emergency flare unless
it maintains a water seal.) We
acknowledge that there are difficulties
and costs with installing monitors on
flares that rarely operate. However, we
are concerned about how the owner or
operator will detect emissions above
500 lb SO2 in any 24-hour period during
an upset or malfunction of a refinery
process unit or ancillary equipment
connected to the flare. Commenters
appear to have conflicting opinions
regarding the ability to sample the flare
gas to determine the sulfur content (or
total sulfur-to-H2S ratio) during a flaring
event. If samples could be taken during
the flaring events, then that would be a
potential option. However, during a
process upset or malfunction, focus
should be on alleviating the problem
rather than taking a special sample.
Also, given the duration of some of
these events, it appears unlikely that
representative samples can be manually
collected.
Taking the difficulties discussed
above into account, we have developed
an alternative monitoring option for
emergency flares. As noted in the
previous response, emergency flares are
expected to properly maintain a water
seal. We provide pressure and water
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seal liquid level monitoring, as
previously described as an alternative to
the sulfur and flow monitors. As
described in more detail above, any fuel
gas pressure exceeding the water seal
liquid level triggers a root cause analysis
and there is a limit to the number of
exceedances in one year. Under this
option, a root cause analysis is triggered,
based on the monitored pressure and
water seal height, so accurate
measurements of flow rate and sulfur
concentrations are less critical than for
flares that must evaluate these
parameters to determine if a root cause
analysis is needed. Consequently, for
these flares, engineering calculations
can be used to estimate the reported
emissions during the flaring event, but
the root cause analysis must be
performed regardless of the magnitude
of these engineering estimates. Using
this alternative monitoring option,
emergency flares are not required to
install continuous sulfur monitoring
systems. Flares that do not meet the
conditions of an emergency flare are
required to install continuous sulfur
monitoring systems and cannot elect
this alternative monitoring option.
We also agree that flaring solely for
the purpose of a RATA or other
performance test is not desirable. The
‘‘cylinder gas audit’’ procedures
requested by the commenter are
described as alternative relative
accuracy procedures in section 16.0 of
Performance Specification 2 (referenced
from Performance Specification 5). We
reviewed the alternative relative
accuracy procedures and considered
how they may apply to flares, and we
have determined that the alternative
relative accuracy procedures are
appropriate for flares. We expect that,
for most affected flares, the variability in
flow (including no flow conditions) and
sulfur content of the gases discharged to
the flare create significant barriers to the
normally required relative accuracy
assessments, particularly if those
assessments need to be made over a
range of sulfur concentrations
potentially seen by the monitor.
Therefore, we are amending 40 CFR
60.107a(e)(1)(ii) and 40 CFR
60.107a(e)(2)(ii) to specify that the
owner or operator of a flare may elect
to use the alternative relative accuracy
procedures in section 16.0 of
Performance Specification 2 of
Appendix B to part 60. As required by
40 CFR 60.108a(b), the owner or
operator shall notify the Administrator
of their intent to use the alternative
relative accuracy procedures.
Comment: One commenter requested
that the EPA clarify whether the
additionally proposed sulfur monitoring
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options for flares are for total reduced
sulfur or total sulfur. The commenter
noted that measuring total sulfur is the
simplest and most inclusive
measurement of SO2 emissions and it is
the method included in SCAQMD Rule
1118. The commenter also requested
that methods for measuring total sulfur
in gaseous fuels be included as
acceptable options to perform the
relative accuracy evaluations of the
CEMS.
One commenter requested that
provisions be made in 40 CFR
60.107a(e)(2) to develop a total sulfurto-H2S (or total reduced sulfur-to-H2S)
ratio so that the total sulfur monitor can
be used for both the root cause analysis
requirements and for compliance with
the requirement to limit short-term H2S
concentration in fuel gas sent to a flare
to 162 ppmv without the need for a
duplicative continuous H2S monitor.
Another commenter supported the
addition of alternative monitoring
methods for the sulfur content of flare
gas, but noted that since the
composition of flare gas is highly
variable, the alternative methods must
meet continuous monitoring
requirements.
Response: We have clarified and
consolidated the monitoring
requirements to allow total reduced
sulfur monitoring for flares. For the
purposes of evaluating the SO2 root
cause analysis threshold, total sulfur
monitoring provides the most accurate
assessment. However, in most cases, the
vast majority of sulfur contained in
gases discharged to the flare is expected
to be in the form of total reduced sulfur
compounds, which include carbon
disulfide, carbonyl sulfide and H2S. Our
test method for measuring total reduced
sulfur includes the use of EPA Method
15A as a reference method, and because
EPA Method 15A measures total sulfur,
the total reduced sulfur monitoring
requirement is equivalent to a total
sulfur monitoring method.
As discussed previously, we are
relying on the suite of flare
requirements we are promulgating to
limit SO2 emissions at the flare. These
include optimizing management of the
fuel gas by limiting the short-term
concentration of H2S to 162 ppmv
during normal operating conditions. We
expected most refineries would already
have the H2S monitor and did not
consider the use of a total sulfur
monitor for use in complying with the
short-term 162 ppmv H2S concentration
in the fuel gas. As the H2S concentration
will always be less than the total
reduced sulfur concentration, it is
acceptable to use the total reduced
sulfur monitor to verify that the fuel gas
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does not exceed the short-term H2S
concentration of 162 ppmv. Therefore,
we have provided for the use of total
reduced sulfur monitors, provided the
monitor can also meet the 300 ppmv
span requirement.
However, we have not provided a
correction factor to scale down the total
reduced sulfur concentration to H2S.
The owner or operator using this
method must essentially be able to
demonstrate they can achieve a 162
ppmv total reduced sulfur concentration
in the fuel gas. The concentration ratio
was provided for the purposes of the
root cause analysis because of the costs
of adding a total sulfur monitoring
system when a dual range H2S monitor
was already in-place, as well as the
expected accuracy needed for the
system to assess the SO2 root cause
analysis threshold. As few cases would
exist where the flaring event would be
right at the SO2 root cause analysis
threshold of 500 lb in any 24-hour
period, inaccuracies associated with the
average total sulfur-to-H2S ratio were
not expected to be significant.
On the other hand, the short-term 162
ppmv H2S concentration in the fuel gas
must be continuously maintained, and
the total sulfur-to-H2S ratio at these low
concentrations is expected to be highly
variable, depending on the efficiency of
the amine scrubber systems. As the
amine scrubber systems, according to
previous industry comments, are not
effective for reduced sulfur compounds
other than H2S, the non-H2S reduced
sulfur concentration is expected to be
fairly constant, with most of the
fluctuations in total sulfur content being
attributable to fluctuations in H2S
concentrations. Consequently, we have
determined that the inaccuracies of the
ratio approach are not acceptable for
continuously demonstrating that the
short-term concentration in the fuel gas
does not exceed 162 ppmv H2S.
Therefore, owners or operators of
affected flares may use the direct output
of a total reduced sulfur monitor to
assess compliance with the short-term
162 ppmv H2S concentration in the fuel
gas, or they must install a continuous
H2S monitor.
Comment: One commenter supported
the proposed amendment revising the
span value for fuel gas H2S analyzers to
match the span requirements in 40 CFR
part 60, subpart J, stating this will save
time and money. However, the
commenter stated that the span value
for the flare H2S monitoring option is
too restrictive and suggested that
requirements in Appendix F to part 60
provide sufficient quality assurance/
quality control (QA/QC) without the
need for the rule to specify the span
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range. The commenter also requested
clarification of the sulfur monitor span
for flares, suggesting that it should be
based on the H2S concentration limits
and that engineering calculations can be
used to assess exceedances of the SO2
root cause analysis threshold of 500 lb
in any 24-hour period.
Response: The H2S span value is at
300 ppmv to verify compliance with the
H2S concentration requirement for the
fuel gas; the span of the total sulfur
monitor needs to be much greater than
that to be able to quantify the sulfur
content in streams containing several
percent sulfur. For units that use the
H2S analyzers both to assess compliance
with the short-term 162 ppmv H2S
concentration requirement for the fuel
gas and to assess exceedances of the SO2
root cause analysis threshold of 500 lb
in any 24-hour period, a dual range
monitor will be necessary. For the
purposes of the SO2 root cause analysis
threshold of 500 lb in any 24-hour
period, we intended that the monitor be
capable of accurately determining the
sulfur concentration for the range of
concentrations expected to be seen at
the flare. We are particularly interested
in quantifying the concentrations of
high sulfur-containing streams as these
would be the streams most likely to
trigger a root-cause analysis at low
flows. We proposed that the span for the
flare sulfur monitor be selected from a
range of 1 to 5 percent. We agree with
the commenter that this may be too
restrictive, and we have revised the
span requirements to be determined,
based on the maximum sulfur content of
gas that can be discharged to the flare
(e.g., roughly 1.1 to 1.3 times the
maximum anticipated sulfur
concentration), but no less than 5,000
ppmv. A single dual range monitor may
be used to comply with the short-term
162 ppmv H2S concentration
requirement for the fuel gas and the SO2
root cause analysis threshold
monitoring requirement provided the
applicable span specifications are met.
In reviewing the span specifications, we
noted that span requirements were
inadvertently omitted from the total
reduced sulfur compound monitoring
alternative. The purpose of these
monitors is identical to the H2S
monitoring alternative, and the same
span considerations apply for these
monitors.
We disagree that the QA/QC
procedures in Appendix F to part 60 are
sufficient without specifying the span
values. Procedure 1 of Appendix F to
part 60 defines ‘‘span value’’ as: ‘‘The
upper limit of a gas concentration
measurement range that is specified for
affected source categories in the
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applicable subpart of the regulation.’’
The concentrations used for calibration
are based on the span value. Several of
the QA/QC procedures in Appendix F
are undefined if the span value is not
defined in the rule.
Comment: Commenters stated that
time is needed to install continuous
monitors and to make other necessary
changes (such as installing a flare gas
recovery system or additional amine
treatment) to comply with all the flare
requirements (e.g., limiting short-term
H2S concentration to 162 ppmv, longterm 60 ppmv H2S fuel gas
concentration limit, flare management
plan, root cause analysis and
continuous monitoring), especially
considering how quickly a flare may
become a modified affected source.
While most commenters focused on the
amount of time needed to install
equipment to comply with the long-term
60 ppmv H2S fuel gas concentration
limit, other commenters asserted that
additional time for activities, such as
planning and re-piping, would be
needed to meet the standards.
Commenters requested differing
amounts of additional time generally
ranging from 3 to 5 years. Commenters
noted that the additional time would
allow owners and operators to schedule
any process unit shutdowns needed to
install new equipment or monitors
during a turnaround. One commenter
recommended that the extra time to
begin root cause analyses provided to
refiners committing to install flare gas
recovery systems should also be
provided to refiners committing to
expand an existing flare gas recovery
system. Commenters also noted that
experience implementing SCAQMD
Rule 1118 suggests that there will be
difficulty obtaining and installing
continuous monitors in less than 3 years
due to the availability of monitor
manufacturers and the need to stage the
installation of monitors at refineries
with multiple affected flares. One
commenter requested that the EPA
consider a compliance schedule in 40
CFR part 60, subpart Ja that is consistent
with compliance schedules in consent
decrees. Commenters objected to
phasing out the additional time after the
rule has been in place for 5 years.
One commenter requested
clarification regarding the trigger date
from which the additional time to
comply with the flare provisions (e.g., 2
years when installing a flare gas
recovery system) begins. The
commenter questioned whether the
trigger date is when construction starts,
at startup or when the stay is removed
(or whichever is later). Another
commenter agreed that the EPA should
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set the compliance time based on the
initial startup of the modification. The
commenter noted that the EPA should
follow the 40 CFR part 60 General
Provisions for performance test timing
and the 40 CFR part 63 General
Provisions for compliance timing.
Response: As we are no longer
applying the long-term 60 ppmv H2S
fuel gas concentration limit to flares, the
comments related to the amount of time
needed to comply with a long-term 60
ppmv H2S fuel gas concentration limit
are moot. We do, however, recognize
that a flare modification can occur much
more quickly than modifications of
traditional process-related emission
sources. Therefore, we evaluated the
comments regarding the amount of time
needed to meet the various
requirements for flares while keeping
the 40 CFR part 60, subpart Ja flare
modification provision in mind. We
discuss each requirement and the time
for demonstrating compliance with that
requirement in the following
paragraphs.
We find it appropriate to require
modified flares that already have
adequate treatment and monitoring
equipment in place to achieve a shortterm H2S concentration of 162 ppmv
(resulting from compliance with 40 CFR
part 60, subpart J) to continue to meet
that concentration upon startup of the
affected flare or the effective date of this
final rule, whichever is later. However,
some flares are not affected facilities
subject to 40 CFR part 60, subpart J, and
others are complying with subpart J
requirements as specified in consent
decrees or have received alternative
monitoring plans by which to
demonstrate compliance with the shortterm H2S concentration limit. In these
cases, we find it appropriate to allow
more time to comply with the shortterm H2S concentration limit and/or the
associated monitoring requirements
because additional amine treatment
and/or monitoring systems will be
required to comply with the rule.
Therefore, the final rule requires all
modified flares that are newly subject to
40 CFR part 60, subpart Ja (but were not
previously subject to 40 CFR part 60,
subpart J) to comply with the short-term
H2S concentration limit and applicable
monitoring requirements no later than 3
years after the effective date of this final
rule or upon startup of the affected flare,
whichever is later. Modified flares that
have accepted applicability of subpart J
under a federal consent decree shall
comply with the subpart J requirements
as specified in the consent decree but
shall comply with the short-term H2S
concentration limit and applicable
monitoring requirements no later than 3
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years after the effective date of this final
rule. Modified flares that are already
subject to the 162 ppmv short-term H2S
concentration limit under subpart J
must meet the short-term H2S
concentration limit under subpart Ja
upon startup of the affected flare or the
effective date of this final rule,
whichever is later. Finally, modified
flares that are already subject to the
short-term H2S concentration limit but
that have an approved monitoring
alternative under subpart J and do not
have the monitoring equipment in-place
that is required under subpart Ja shall be
given up to 3 years from the effective
date of this final rule to install the
monitors required by subpart Ja (or to
obtain an approved monitoring
alternative under subpart Ja).
As we noted in the preamble to the
proposed amendments, many of the
connections that would trigger
applicability to 40 CFR part 60, subpart
Ja are critical to the safe and efficient
operation of the refinery. These
connections can, and often must, be
installed quickly. At the same time,
nearly all refineries will need time for
planning, designing, purchasing and
installing (including any necessary repiping) sulfur and flow monitors that
are newly required by subpart Ja. Some
refineries will elect to add flare gas
recovery and/or sulfur treatment
equipment to minimize their emissions
as part of the evaluations conducted, as
required by the new flare management
plan requirements, and time will be
needed for planning, designing,
purchasing and installing these
components as well. Given that many
flares will become modified affected
sources relatively quickly, owners and
operators will be competing with one
another for the services and products of
a finite number of vendors who provide
the necessary monitors and other
equipment. Several commenters
specifically noted availability of
monitors as an issue when complying
with SCAQMD Rule 1118. As such, we
find that immediate compliance with
the requirements for flares, such as the
planning, designing, purchasing and
installation of (including any necessary
re-piping) sulfur and flow monitors,
may be difficult for operators to meet,
especially in situations where quick
connections to the flare are made. A
phased compliance schedule allows for
the operators to comply with some
requirements associated with flares,
such as continuing to achieve a shortterm H2S concentration of 162 ppmv, if
the flares are already subject to 40 CFR
part 60, subpart J and have adequate
monitoring in place to comply with this
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final rule, while allowing time to install
treatment and processing equipment
and monitoring equipment to comply
with the standards where necessary.
A phased compliance schedule will
also allow owners and operators to
minimize process interruption by
coordinating the installation of
monitoring equipment with process
shutdowns or turnarounds. In addition
to providing operating flexibility to the
refinery, we are taking into
consideration the fact that a process
shutdown and subsequent startup can
generate significant emissions, even if
the refinery is taking care to minimize
those emissions. We consider a phased
compliance schedule that allows owners
and operators to avoid startups and
shutdowns that are not necessary to
maintain the equipment and process to
be environmentally beneficial overall
and the best system of emissions
reduction for a quickly modified flare.
Considering the time needed to
complete engineering specifications,
order and install the required
monitoring equipment, and considering
the need to coordinate this installation
with process unit shutdown or
turnarounds, we determined that
completion of these activities within 3
years is consistent with the best system
of emissions reductions for quickly
modified flares.
We note, however, that this phased
compliance schedule for the flare
requirements in 40 CFR part 60, subpart
Ja is intended for those situations when
a flare modification occurs quickly and
the owner or operator does not have
significant planning opportunities to
install the required monitors or
implement the selected flare
minimization options without
significant process interruptions. For a
future large project on a schedule that
includes time for planning, designing,
purchasing and installing equipment
and monitors, we expect that the owner
and operator will have time to assess
whether or not the refinery flares will
become affected sources through
modification. If a project will result in
the modification of a flare, we expect
that the owner or operator will then
plan how to meet the standards in
subpart Ja as part of the project itself,
including the installation of the
monitoring systems and the
development of a flare management
plan. Because of the ability to plan
ahead, flares that are modified as part of
a large project will not have all of the
difficulties meeting the subpart Ja flare
requirements upon completion of the
modification as those flares that are
modified quickly. Therefore, we find
that compliance with the flare
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requirements upon startup of the
modified flare is appropriate and
consistent with the best system of
emissions reduction for large projects
resulting in a modification of a flare.
Thus, we determined that the
appropriate time period for compliance
with the flare standards is either: (1) 3
years from the effective date of these
amendments or (2) upon startup of the
modified flare, whichever is later.11 In
this manner, flares that become subject
to subpart Ja quickly, based on a small
safety-related connection (or have
already become subject to subpart Ja
based on a modification prior to the
effective date of these amendments),
will have up to 3 years from the
effective date of these amendments to
comply fully with the flare standards,
but flares that are modified as the result
of a significant project, such as the
installation of a new process unit that
will be tied into an existing flare, will
effectively be required to comply with
the flare standards at the startup of the
new process unit.
Therefore, for the reasons described
above, we are providing flares that
become affected facilities subject to 40
CFR part 60, subpart Ja through
modification with a phased compliance
schedule for the flare standards, as
described in this paragraph. The final
rule requires owners and operators of
modified flares to meet the short-term
162 ppmv H2S concentration
requirement by the effective date of
these amendments or upon startup of
the affected flare (whichever is later)
only if they are already subject to the
short-term 162 ppmv H2S concentration
limit in 40 CFR part 60, subpart J.
Modified flares that were not affected
flares under subpart J prior to being
modified facilities under subpart Ja
must comply with the short-term 162
ppmv H2S concentration requirement
within 3 years of the effective date of
these amendments or upon startup of
the modified flare, whichever is later.
Owners and operators of modified flares
that are have accepted applicability of
subpart J under a federal consent decree
shall comply with the subpart J
requirements as specified in the consent
decree, but must meet the short-term
162 ppmv H2S concentration limit no
later than 3 years after the effective date
of this final rule. Owners and operators
of modified flares that are already
subject to subpart J and that have an
approved monitoring alternative and are
11 For the purposes of this subpart, startup of the
modified flare occurs when any of the activities in
40 CFR 60.100a(c)(1) or (2) is completed (e.g., when
a new connection is made to a flare such that flow
from a refinery process unit or ancillary equipment
can flow to the flare via that new connection).
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unable to meet the applicable subpart Ja
monitoring requirements for the shortterm H2S concentration limit must meet
the short-term H2S concentration
requirement upon startup of the affected
flare or the effective date of this final
rule, whichever is later, but shall be
given up to 3 years from the effective
date of this final rule to install the
monitors required by subpart Ja. In this
interim period, owners and operators of
these modified flares shall demonstrate
compliance with the short-term H2S
concentration limit using the
monitoring alternative approved under
subpart J.
Additionally, we are requiring owners
and operators of modified flares to
complete and implement the flare
management plan under 40 CFR
60.103a(a) by 3 years from the effective
date of these amendments or upon
startup of the modified flare, whichever
is later. We are requiring owners and
operators of modified flares to begin
conducting root cause and corrective
action analyses under 40 CFR 60.103a(c)
and (d) no later than 3 years from the
effective date of these amendments or
the date of the startup of the modified
flare, whichever is later, so that the
facility can complete the flare
management plan and establish baseline
flow rates prior to performing the root
cause and corrective action analyses.
We are also requiring owners and
operators of modified flares to install
and begin operating the monitors
necessary to demonstrate compliance
with these provisions, as required under
40 CFR 60.107a(e) through (g) within 3
years from the effective date of these
amendments or by the startup date of
the modified flare, whichever is later,
when the monitors are not already in
place. Compliance with the phased
compliance schedule constitutes
compliance with the flare standards as
of the effective date.
We note that the final rule does not
provide a phased compliance schedule
for new and reconstructed flares. The
final rule requires owners and operators
of new and reconstructed flares to meet
all the flare requirements, including the
short-term 162 ppmv H2S concentration
requirement, upon the effective date of
the requirements or upon startup of the
affected flare, whichever is later.
C. Other Comments
Comment: Several commenters
objected to the change to the definition
of ‘‘refinery process unit.’’ The
commenters objected to the proposed
amendments to include coke
gasification, loading and wastewater
treatment, stating the change makes the
term more expansive. The commenters
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stated that the EPA did not evaluate the
impacts or explain the consequences of
the revised definition. One commenter
stated that product loading is generally
considered part of the refinery process
unit to which it is associated and that
wastewater treatment is a utility.
Another commenter suggested that the
definition specify SIC 2911 (as in
Refinery MACT 1).
Response: The original definition of
‘‘refinery process unit’’ in 40 CFR part
60, subpart J and the definition of
‘‘refinery process unit’’ promulgated in
40 CFR part 60, subpart Ja in June 2008
read as follows: ‘‘Refinery process unit
means any segment of the petroleum
refinery in which a specific processing
operation is conducted.’’ Thus, to be
considered a refinery process unit, only
two criteria are needed: (1) The unit
must be located at a petroleum refinery;
and (2) the unit must be used to conduct
‘‘a specific processing operation.’’ The
definition does not directly limit the
scope of ‘‘processing operations.’’ That
is, the definition of refinery process unit
does not limit process operations to
distillation, re-distillation, cracking or
reforming, and it is not limited to only
those processes used to produce
gasoline, kerosene, fuel oils, etc. In the
proposed amendment to this definition,
we listed ‘‘operations’’ that we
construed as conducting a ‘‘specific
processing operation’’ when these
operations are located at a petroleum
refinery. Consequently, we considered
the proposed inclusion of examples of
refinery process units to be a
clarification of the existing definition
rather than an expansion of the original
definition.
We reviewed the impact of the
proposed revision of this definition on
40 CFR part 60, subpart Ja, as well as its
historic use in 40 CFR part 60, subpart
J. The term ‘‘refinery process unit’’ is
used primarily in the definitions of
certain affected facilities, ‘‘process gas’’
and ‘‘process upset gas’’ in subparts J
and Ja. The term is also used in the flare
provisions in subpart Ja. With respect to
the definitional terms, there can be no
issue with including the designation of
‘‘refinery process unit’’ within the
definitions for specific process units.
‘‘Process gas’’ is not used at all in either
rule, although it was revised between
proposal and promulgation of subpart J.
In response to a comment that the
definition of ‘‘process gas’’ ‘‘should
have included the non-hydrocarbon
gases produced by various process units
in a refinery,’’ the EPA responded: ‘‘The
definition has been revised to include
all gases produced by process units in
a refinery except fuel gas and process
upset gas.’’ (See page 127 of Background
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Information for New Source
Performance Standards, Volume 3,
Promulgated Standards (BID Vol. 3),
EPA 450/2–74–003 (Feb. 1974), Docket
Item No. EPA–HQ–OAR–2007–0011–
0082). The definition had actually been
revised to include ‘‘any gas generated by
a petroleum refinery process unit.’’ The
response in BID Vol. 3 suggests that the
EPA considered ‘‘refinery process units’’
and ‘‘process units in a refinery’’ to have
the same meaning, and there is no
mention of limiting what is considered
to be a ‘‘refinery process unit’’ or a
‘‘process units in a refinery.’’
‘‘Process upset gas’’ is used only to
provide an exemption to the H2S
concentration limit for process upset gas
sent to a flare. See 40 CFR 60.104(a)(1),
60.103a(h). Therefore, a narrow
definition of ‘‘refinery process unit’’
would only limit those gases sent to a
flare that would qualify as ‘‘process
upset gas.’’ For example, if a coke
gasifier is not a refinery process unit,
then gases generated during the startup,
shutdown or malfunction of a coke
gasifier located at the refinery would not
be ‘‘process upset gas’’ and would be
required to comply with the
requirement to limit short-term H2S
concentration in fuel gas to 162 ppmv
if sent to a flare. We find that the
historical application of the ‘‘process
upset gas’’ exclusion has considered a
broad definition of what constitutes a
‘‘refinery process unit.’’
For 40 CFR part 60, subpart Ja, the
definition of ‘‘refinery process unit’’
also impacts the flare provisions. Based
on the proposed revisions of ‘‘refinery
process unit,’’ it was clearly our intent
that a broad definition of ‘‘refinery
process unit’’ should apply to the flare
requirements. Specifically, we intended
that a flare modification occurs when a
wide range of equipment at the
petroleum refinery is newly connected
to the flare. It was also our intent that
the flare management plan consider
flare minimization methods for this
broadly defined range of equipment
referred to collectively as ‘‘refinery
process units.’’
Based on our review of the impacts of
changes to the definition of ‘‘refinery
process unit,’’ and considering all of the
comments received, we maintain that
the existing definition of ‘‘refinery
process unit’’ is broad and should be
broadly interpreted. For consistency
between 40 CFR part 60, subparts J and
Ja, we have elected to maintain the
existing definition and not include an
example list of refinery process units
within the definition. However, to
clarify that a modification to a flare
occurs when these types of equipment
are connected to the flare, we revised
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the language in the flaring provisions to
refer to ‘‘refinery process units,
including ancillary equipment.’’ This
revision is made to clarify our original
intent that coke gasification units,
storage tanks, product loading
operations and wastewater treatment
systems, as well as pressure relief
valves, pumps, sampling vents,
continuous analyzer vents and other
similar equipment are units from which
a connection to a flare would trigger a
flare modification and generate gas
streams that should be considered in the
flare management plan. We have
included in the final amendments a
definition of ‘‘ancillary equipment.’’
Specifically, ancillary equipment means
equipment used in conjunction with or
that serve a refinery process unit.
Ancillary equipment includes, but is not
limited to, storage tanks, product
loading operations, wastewater
treatment systems, steam- or electricityproducing units (including coke
gasification units), pressure relief
valves, pumps, sampling vents, and
continuous analyzer vents.
Sulfur recovery plants are also units
from which a connection to a flare
would trigger a flare modification and
generate gas streams that should be
considered in the flare management
plan. We recognize that on-site sulfur
recovery plants are considered refinery
process units, and we proposed
amendments to the definitions of
‘‘refinery process unit’’ and ‘‘sulfur
recovery plant’’ to clarify that we
consider a sulfur recovery plant to be ‘‘a
segment of the petroleum refinery in
which a specific processing operation is
conducted.’’ However, the strict
definition of ‘‘refinery process unit’’
would only apply to sulfur recovery
plants physically located at the refinery.
As 40 CFR part 60, subpart Ja also
applies to off-site sulfur recovery plants
(see 40 CFR 60.100(a) and 40 CFR
60.100a(a)), we found it potentially
contradictory to define a sulfur recovery
plant located outside the refinery as a
‘‘refinery process unit,’’ so we are also
not finalizing the proposed amendment
to include the term ‘‘all refinery process
units’’ in the definition of ‘‘sulfur
recovery plant.’’ However, while
connections to a refinery flare from an
off-site sulfur recovery plant are not
expected to be common, off-site sulfur
recovery plants are subject to subpart Ja.
We clarify in this response that we
would consider such a connection to a
flare to be from a ‘‘refinery process unit,
including ancillary equipment,’’ such
that connecting an off-site sulfur
recovery plant that is subject to subpart
Ja to a flare at a refinery would cause
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that flare to be a modified flare subject
to subpart Ja.
Further, in reviewing the definition of
‘‘sulfur recovery plant,’’ we noticed an
inadvertent error that also suggests that
the sulfur recovery plant must be
located at a petroleum refinery, which is
not consistent with the applicability
provisions in 40 CFR 60.100(a) and 40
CFR 60.100a(a). Specifically, we
inadvertently omitted the word
‘‘produced’’ in this first sentence, so we
are amending the definition of ‘‘sulfur
recovery plant’’ to clarify that a sulfur
recovery plant recovers sulfur from sour
gases ‘‘produced at the petroleum
refinery.’’ Thus, we are amending the
definition of ‘‘sulfur recovery plant’’ to
correct inadvertent errors and to clarify
that off-site sulfur recovery plants are
included in the definition of ‘‘sulfur
recovery plant,’’ as these plants are
expressly considered to be affected
facilities in 40 CFR part 60, subpart Ja.
Comment: Commenters supported the
revised definition of ‘‘delayed coking
unit,’’ but stated that, since 40 CFR part
60, subpart Ja only sets standards for the
coke drums, the definition should just
include the coke drums associated with
a single fractionator. The commenters
stated that the definition should not
include the fractionator itself because
VOC emissions from the fractionator are
covered by NSPS for equipment leaks.
Response: The proposed amendments
to the definition of ‘‘delayed coking
unit’’ specifically listed the primary
components of the delayed coking unit.
In particular, based on the operation of
the delayed coking unit, we find that the
fractionator is an integral part of the
delayed coking unit. The fresh feed to
the delayed coking unit is generally
introduced in the fractionator tower
bottoms receiver. This integral use of
the fractionator is different than the use
of fractionators used for other units
defined in 40 CFR part 60, subpart Ja,
such as the fluid catalytic cracking unit
(FCCU). For the FCCU, fresh feed is
introduced in the riser, which is part of
the affected facility in subpart Ja. As the
feed to the delayed coking unit is to the
fractionator, we find that the
fractionator is an integral part of the
delayed coking unit, so we specifically
include it as part of the affected facility.
While our proposed amendments
covered only the major components of
the delayed coking unit, upon our
review of the definition based on the
comments received, we note that there
are several other components of the
delayed coking unit that are integral to
the operation of the delayed coking unit.
Additionally, even though the standards
are specific to the coke drum, many of
these integral components are
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interconnected and necessary for the
delayed coking unit to meet the
applicable standards. Based on our
review of the operation of a delayed
coking unit, we also include coke
cutting and blowdown recovery
equipment in the final definition
because this equipment is also integral
to the overall cyclical operation of the
process unit. The definition of ‘‘delayed
coking unit’’ has been amended in the
final rule to mean a refinery process
unit in which high molecular weight
petroleum derivatives are thermally
cracked and petroleum coke is produced
in a series of closed, batch system
reactors. A ‘‘delayed coking unit’’
includes, but is not limited to all of the
coke drums associated with a single
fractionator; the fractionator, including
bottoms receiver and overhead
condenser; the coke drum cutting water
and quench system, including the jet
pump and coker quench water tank;
process piping and associated
equipment such as pumps, valves and
connectors; and the coke drum
blowdown recovery compressor system.
Since this definition is more specific
than the definition included in the
amendments proposed on December 22,
2008, it could affect which delayed
coking units are subject to subpart Ja.
For example, an owner or operator may
have made a change to a delayed coking
unit that would not be considered a
modification under the December 22,
2008, definition, but that same change
could make the delayed coking unit a
modified facility subject to subpart Ja
using the definition of ‘‘delayed coking
unit’’ above. In other words, in changing
the definition of ‘‘delayed coking unit’’
in the final rule, some delayed coking
units that would not have been affected
sources under the proposed
requirements might now be covered by
the final rule. Under CAA section
111(a)(2), a ‘‘new source’’ is defined
from the date of proposal only if there
is a standard ‘‘which will be applicable
to such source;’’ otherwise, a ‘‘new
source’’ is defined based upon the final
rule date. In this circumstance, using
the proposal date as the new source date
for determining applicability for this
group of delayed coking units would be
inappropriate as such units would not
have been on notice that subpart Ja
could apply to them. Accordingly, we
moved the ‘‘new source’’ date for this
group of delayed coking units so that
delayed coking units that are only
defined as such under the final rule are
covered by the final rule only if they
commence construction, reconstruction
or modification after the promulgation
date of these final amendments. The
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‘‘new source’’ date for other delayed
coking units will depend on the
previous definitions and when the
activities involving the delayed coking
unit occurred. See § 60.100a(b) for
determining applicability of subpart Ja
for delayed coking units.
Comment: One commenter stated that
40 CFR part 63, subpart LLLLL indicates
at 40 CFR 63.8681(e) that 40 CFR part
60, subpart J does not apply for asphalt
blowing stills subject to subpart LLLLL,
and the commenter requested similar
clarification for 40 CFR part 60, subpart
Ja by exempting this process in 40 CFR
60.100a.
Response: We reviewed the
requirement in 40 CFR part 63, subpart
LLLLL. Due to the O2 content of this
process gas, we agree that it is not
suitable for recovery as fuel gas and
subsequent amine treatment; therefore,
it is not BSER for combustion controls
used on asphalt blowing stills to meet
the H2S concentration limits (or
alternative SO2 emissions limits). We
reviewed 40 CFR 60.100a, but we feel a
blanket exemption from 40 CFR part 60,
subpart Ja is not necessary. Instead, we
have included an exemption within the
definition of fuel gas similar to the
exemptions included for combustion
controls on vapors collected and
combusted from wastewater treatment
and marine vessel loading operations.
Specifically, we amended the definition
of fuel gas in 40 CFR 60.101a to clarify
that fuel gas does not include vapors
that are collected and combusted to
control emissions from asphalt
processing units (i.e., asphalt blowing
stills).
Comment: One commenter
recommended that the exclusion from
the definition of ‘‘fuel gas’’ be extended
to vapors ‘‘from marine vessel loading
operations or waste management units
that are collected and combusted’’
without any reference to a federal
requirement. At a minimum, the
commenter stated that marine benzene
loading under 40 CFR part 61, subpart
BB; the wastewater provisions of 40 CFR
part 63, subpart G; remediation efforts
regulated under Resource Conservation
and Recovery Act (RCRA) corrective
action; and RCRA 7003 orders should be
added to the exclusion.
Response: We were originally
concerned that removing the reference
to a federal standard may inadvertently
exempt the use of these vapors when
used in process heaters or boilers. We
determined that it was not BSER to
require thermal oxidizers used to
comply with the cited federal standards
to comply with the H2S concentration
limits due to the typically remote
location of the combustion sources
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56453
(control devices) relative to refinery
process units (see technical
memorandum entitled Fuel Gas
Treatment of Marine Vessel Loading
and Wastewater Treatment Unit Off-gas,
in Docket ID No. EPA–HQ–OAR–2007–
0011). However, if these gases are
currently routed to a fuel gas system or
directly to a process heater or boiler,
treatment of the fuel gas to meet the SO2
emissions limits or the H2S
concentration limits is expected to be
economically viable. Additionally, these
gases are expected to be only a small
portion of the fuel gas combusted in
these units, and the refinery has an
option to over-treat the primary fuel gas
so that gases from the wastewater
treatment system or marine vessel
loading operation can remain untreated
while the fuel gas combustion device
itself can comply with the SO2
emissions limits or the H2S
concentration limits, based on the
mixture of fuels used in the device.
In reviewing the rules suggested by
the commenter, as well as those we
originally listed, we noted that
acceptable ‘‘control devices’’ or
‘‘combustion units’’ in these rules
include process heaters and boilers. We
did not intend to exclude vapors that
are collected and routed to a process
heater or boiler to be exempt from the
definition of fuel gas. In other words,
when developing this exclusion, we
specifically considered the combustion
of these gases via a thermal oxidizer or
flare currently located at the marine
vessel loading or wastewater treatment
location. These remote combustion
devices were really the subject of the
analysis, but we did not want to exclude
these combustion units themselves
because other fuel gas is often fed to
these units to ensure adequate
combustion of the vapors being
controlled. It is clear from our rationale
and the description of the exemption
included in the preamble of the
proposed rule that the exemption was
intended ‘‘to exempt vapors that are
collected and combusted in an air
pollution control device installed to
comply with’’ specific wastewater or
marine vessel loading emissions
standards. (72 FR 27180 and also at
27183) Process heaters or boilers would
not be ‘‘installed’’ to comply with these
provisions, and it was not our intent to
exclude vapors sent to these types of
combustion units. However, the
regulatory text is more ambiguous and
appears to exclude any vapors collected
and combusted, regardless of where
they are combusted. As such, we are
amending this exclusion to better
represent our original intent.
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Additionally, with the added clarity
in the regulatory text, it seems
appropriate to extend this exclusion to
control devices used at these locations
regardless of why the emission controls
were installed. That is, while we
originally considered air pollution
control devices that were mandated by
the EPA, we see no reason to
discriminate against air pollution
control devices that were installed
voluntarily to reduce the emissions from
these sources. Further, we intend to
clarify that gases off the sour water
system, including the sour water
stripper, would likely contain higher
amounts of reduced sulfur and would be
economically viable to treat. Therefore,
we are also clarifying that the
exemption does not extend to the sour
water system. Therefore, the amended
definition of ‘‘fuel gas’’ in both 40 CFR
part 60, subparts J and Ja states that fuel
gas ‘‘does not include vapors that are
collected and combusted in a thermal
oxidizer or flare installed to control
emissions from wastewater treatment
units other than those processing sour
water, marine tank vessel loading
operations, or asphalt processing units
(i.e., asphalt blowing stills).’’
With respect to remediation efforts
conducted under RCRA corrective
actions, we are unwilling to grant such
an exclusion from the definition of ‘‘fuel
gas’’ in 40 CFR part 60, subpart Ja. First,
we anticipate that most vapors from
remediation efforts would be low in
sulfur and, if so, the owner or operator
could apply for the alternative
monitoring methods provided in the
rule. Also, although some remediation
efforts may occur in remote locations,
many of the remediation efforts are
conducted in reasonable proximity to
existing process units. Finally, the range
of activities included in RCRA
remediation efforts is broad, and we
have little information regarding the
number and types of RCRA remediation
activities that are being conducted. The
commenter provided no description of
such activities, nor did they provide a
reasonable rationale as to why the
vapors from these activities should be
exempted.
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V. Summary of Cost, Environmental,
Energy and Economic Impacts
A. What are the emission reduction and
cost impacts for the final amendments?
The emission reduction and cost
impacts presented in this section for
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flares are revised estimates for the
impacts of the final requirements of 40
CFR part 60, subpart Ja for flares, as
amended by this action. The table
shows the differences in anticipated
impacts between these final
amendments to subpart Ja and the final
June 2008 NSPS requirements of subpart
Ja, which were estimated assuming only
40 flares would trigger applicability to
the rule. The impacts are presented for
400 affected flares that commence
construction, reconstruction or
modification that will be required to
comply with this final rule. We
anticipate that most of the flares would
become affected due to the modification
provisions for flares set forth in the final
June 2008 subpart Ja rule. For this
analysis, we assumed that 90 percent of
the flares will be modified or
reconstructed and 10 percent of the
flares will be newly constructed.
Further, we estimate that 30 percent of
the 400 affected flares, or 120 flares,
either would meet the definition of
‘‘emergency flare’’ in subpart Ja or
would be equipped with a flare gas
recovery system such that robust sulfur
and flow monitoring would not be
required. Therefore, the values in Table
5 of this preamble include the costs and
emissions reductions for 400 flares to
comply with the flare management plan
and root cause and corrective action
analyses requirements and for 280 flares
to comply with the sulfur and flow
monitoring requirements. The cost and
emissions reductions for the affected
flares to comply with the short-term H2S
concentration of 162 ppmv in the fuel
gas are included in the baseline rather
than the incremental impacts because
this limit is unchanged from the
requirements in 40 CFR part 60, subpart
J. For further detail on the methodology
of these calculations, see
Documentation of Impact Estimates for
Fuel Gas Combustion Device and Flare
Regulatory Options for Amendments to
the Petroleum Refinery NSPS, in Docket
ID No. EPA–HQ–OAR–2007–0011.
We estimate that the final
requirements for flares will reduce
emissions of SO2 by 3,200 tons/yr, NOX
by 1,100 tons/yr and VOC by 3,400 tons/
yr from the baseline. The estimated
annual cost, including annualized
capital costs, is a cost savings of about
$79 million (2006 dollars) due to the
replacement of some natural gas
purchases with recovered flare gas and
the retention of intermediate and
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Fmt 4701
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product streams due to a reduction in
the number of malfunctions associated
with refinery process units and ancillary
equipment connected to the flare. Note
that not all refiners will realize a cost
savings since we only estimate that
refineries with high flare flows will
install vapor recovery systems.
Although the rule does not specifically
require installation of flare gas recovery
systems, we project that owners and
operators of flares receiving high waste
gas flows will conclude, upon
installation of monitors, implementation
of their flare management plans, and
implementation of root causes analyses,
that installing flare gas recovery would
result in fuel savings by using the
recovered flare gas where purchased
natural gas is now being used to fire
equipment such as boilers and process
heaters. The flare management plan
requires refiners to conduct a thorough
review of the flare system so that flare
gas recovery systems are installed and
used where these systems are
warranted. As part of the development
of the flare management plan, refinery
owners and operators must provide
rationale and supporting evidence
regarding the flare waste gas reduction
options considered, the quantity of flare
gas that would be recovered or
prevented by the option, the BTU
content of the flare gas and the ability
or inability of the reduction option to
offset natural gas purchases. In addition,
consistent with Executive Order 13563
(Improving Regulation and Regulatory
Review, issued on January 18, 2011), for
facilities implementing flare gas
recovery, we are finalizing provisions
that would allow the owner or operator
to reduce monitoring costs and the
number of root cause analyses,
corrective actions, and corresponding
recordkeeping and reporting they would
need to perform. We estimate that the
final requirements for flares will reduce
emissions of SO2 by 3,200 tons/yr, NOX
by 1,100 tons/yr and VOC by 3,400 tons/
yr from the baseline. The overall cost
effectiveness is a cost savings of about
$10,000 per ton of combined pollutants
removed. The estimated nationwide 5year emissions reductions and cost
impacts for the final standards are
summarized in Table 5 of this preamble.
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56455
TABLE 5—NATIONAL EMISSION REDUCTIONS AND COST IMPACTS FOR PETROLEUM REFINERY FLARES SUBJECT TO
AMENDED STANDARDS UNDER 40 CFR PART 60, SUBPART JA
[Fifth year after the effective date of these final rule amendments] a
Subpart Ja requirements
Estimates from June
2008 Final Rule ......
Revised Estimates for
Amendments ..........
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a All
Total capital
cost
($1,000)
Total annual
cost without
credit
($1,000/yr)
Natural gas
offset/product recovery
credit
($1,000)
Total annual
cost
($1,000/yr)
Annual
emission reductions
(tons SO2/
yr)
Annual
emission reductions
(tons NOX/
yr)
Annual
emission reductions
(tons VOC/
yr)
Cost effectiveness
($/ton emissions reduced)
40,000
....................
....................
(7,000)
80
6
200
(23,000)
460,000
100,000
(180,000)
(79,000)
3,200
1,100
3,400
(10,000)
costs in this table are relative to the baseline used for the 2008 final rule.
We also estimate that the final
requirements for flares will result in
emissions reduction co-benefits of CO2
equivalents by 1,900,000 metric tonnes
per year, predominantly as a result of
our estimate of the largest flares
employing flare gas recovery and to a
lesser extent, as a result of the root
cause analyses applicable to all flares.
The cost, environmental and
economic impacts for the final
amendments to 40 CFR part 60, subpart
Ja for process heaters are not expected
to be different than those reported for
the final June 2008 standards. We
expect owners and operators to install
the same technology to meet these final
amendments that we anticipated they
would install to meet the June 2008
final subpart Ja requirements (i.e., ultralow NOX burners). We did revise our
emission estimates based on the type of
process heater, creating separate
impacts for forced draft process heaters
and natural draft process heaters.
Dividing process heaters into separate
subcategories, based on the draft type,
required us to develop new
distributions of baseline emissions for
each type of process heater. The
baseline emission estimates for natural
draft process heaters are slightly lower
than those developed for the existing
subpart Ja requirements (per affected
process heater), but the average
emission reduction achieved by ultralow NOX burners was adjusted to 80
percent (rather than 75 percent used for
generic process heaters). For forced draft
process heaters, the baseline (i.e.,
uncontrolled) emissions rate for forced
draft process heaters was revised
slightly upward, based on the available
emissions data. Due to these differences,
the mix of controls needed to meet a 40
ppmv emissions limit was no longer
cost effective for forced draft process
heaters, but the emission reductions
associated with process heaters
complying with the 60 ppmv standard
were higher than those previously
estimated for generic process heaters.
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Thus, the creation of new subcategories
of process heaters with different
emissions limits for each subcategory
did not impact the control or
compliance methods used by the
facilities (i.e., BSER in all cases was
based on the performance of advanced
combustion monitoring controls in
conjunction with ultra-low NOX
burners) and did not change the
estimated compliance costs. As we do
not have adequate data regarding the
prevalence of natural draft process
heaters versus forced draft process
heaters that will become subject to the
rule, we used the emission reductions
estimated for the two different types of
process heaters as a means to bound the
range of anticipated NOX emission
reductions to be from 7,100 to 8,600
tons/yr in the fifth year after the
effective date of this final rule (see
Revised NOX Impact Estimates for
Process Heaters, in Docket ID No. EPA–
HQ–OAR–2007–0011). We estimated
the emission reductions to be 7,500
tons/yr for the June 2008 final
standards, which falls well within the
anticipated range of emissions
reductions for the standards we are
finalizing here. Given the uncertainty in
the emissions estimates, as well as the
uncertainty in the relative number of
natural draft process heaters versus
forced draft process heaters, we
concluded that the impacts previously
developed for subpart Ja accurately
represent the impacts for process
heaters in these final amendments.
We note that, in the preamble to the
June 2008 final standards, we estimated
costs and emissions reductions for 30
fuel gas combustion devices, but we
subsequently determined that those
estimates did not fully account for the
number of affected flares (which, at the
time, were considered a subset of fuel
gas combustion devices). Therefore, in
the preamble to the December 2008
proposed amendments, we presented
revised emission reduction and cost
estimates for affected fuel gas
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combustion devices. As previously
explained, we are not finalizing the
long-term 60 ppmv H2S fuel gas
concentration limit for flares, as
proposed, and we revised our cost
estimates accordingly. Because these
final amendments consider flares to be
a separate affected source, the emission
reductions and costs for fuel gas
combustion devices are not affected by
these final amendments and are not
included in this preamble. Rather, the
final emission reduction and cost
estimates for fuel gas combustion
devices are very close to the impacts
presented in the June 2008 final rule;
the details of the analysis and the final
impacts are presented in Documentation
of Impact Estimates for Fuel Gas
Combustion Device and Flare
Regulatory Options for Amendments to
the Petroleum Refinery NSPS, in Docket
ID No. EPA–HQ–OAR–2007–0011.
The final amendments to 40 CFR part
60, subpart J are technical corrections or
clarifications to the existing rule and
should have no negative emissions
impacts.
B. What are the economic impacts?
The total annualized compliance costs
are estimated to save about $79 million
(2006 dollars) in the fifth year after the
effective date of these final
amendments. Note that not all refiners
will realize a cost savings as only flare
systems with high waste gas flows
(about 10 percent of all flares) are
expected to install vapor recovery
systems. Alternatively, if no refineries
install flare gas recovery systems, total
annualized compliance costs are
estimated to be $10.7 million (2006
dollars) in the fifth year after proposal.
Regardless of whether any refineries
install flare gas recovery systems, we do
not anticipate any adverse economic
impacts associated with this regulatory
action, as no increase in refined
petroleum product prices or decrease in
refined petroleum product output is
expected.
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
For more information, please refer to
the Regulatory Impact Analysis (RIA)
that is in the docket for this final rule.
monetized benefits of this final
regulatory action to be $270 million to
$580 million (2006 dollars, 3-percent
discount rate) in the fifth year (2017).
C. What are the benefits?
The benefits at a 7-percent discount rate
Emission controls installed to meet
for health benefits and 3-percent
the requirements of this rule will
discount rate for climate benefits are
generate benefits by reducing emissions
$240 million to $530 million (2006
of criteria pollutants and their
dollars). For small flares only, we
precursors, including SO2, NOX and
VOC as well as CO2. SO2, NOX and VOC estimate the monetized benefits are
are precursors to PM2.5 (particles smaller $170 million to $410 million (3-percent
discount rate) and $150 million to $370
than 2.5 microns), and NOX and VOC
million (7-percent discount rate for
are precursors to ozone. For this rule,
we were only able to quantify the health health benefits and 3-percent discount
rate for climate benefits). For large flares
benefits associated with reduced
only, we estimate the monetized
exposure to PM2.5 from emission
benefits are $93 million to $160 million
reductions of SO2 and NOX and the
(3-percent discount rate) and $88
climate benefits associated with CO2
emission reductions. We estimate the
million to $150 million (7-percent
discount rate for health benefits and 3percent discount rate for climate
benefits). Using alternate relationships
between PM2.5 and premature mortality
supplied by experts, higher and lower
benefits estimates are plausible, but
most of the expert-based estimates fall
between these two estimates.12 A
summary of the monetized benefits
estimates by pollutant for all flares at
discount rates of 3 percent and 7
percent is in Table 6 of this preamble.
Several benefits categories, including
direct exposure to SO2 and NOX
benefits, ozone benefits, ecosystem
benefits and visibility benefits are not
included in these monetized benefits.
All estimates are in 2006 dollars for the
year 2017.
TABLE 6—SUMMARY OF THE MONETIZED PM2.5 AND CO2 BENEFITS FOR AMENDED PETROLEUM REFINERIES STANDARDS
[Millions of 2006 dollars] a
Emission reductions (tons per
year)
Pollutant
Total monetized
benefits
(3-percent discount)
Total monetized
benefits
(7-percent discount)
With Flare Gas Recovery
Benefitsb:
PM2.5
SO2 .........................................
NOX ........................................
PM Total .................................
CO2 Benefitsc ..........................
Total Monetized Benefits:
3,200 .............................................
1,100 .............................................
.......................................................
1,900,000d ....................................
$210 to $510 ................................
$7.1 to $18 ...................................
$220 to $530 ................................
$46 ................................................
$190 to $460.
$6.4 to $16.
$190 to $480.
$46.
.......................................................
$260 to $580 ................................
$240 to $520.
Without Flare Gas Recovery
PM2.5 Benefitsb:
SO2 .........................................
NOX ........................................
PM Total .................................
CO2 Benefitsc ..........................
Total Monetized Benefits
2,900 .............................................
56 ..................................................
.......................................................
110,000d .......................................
.......................................................
$190 to $450 ................................
$0.36 to $0.87 ..............................
$190 to $460 ................................
$2.6 ...............................................
$190 to $460 ................................
$170 to $410.
$0.32 to $0.78.
$170 to $410.
$2.6.
$170 to $410.
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a All estimates are for the analysis year (2017) and are rounded to two significant figures so numbers may not sum across rows. The total
monetized benefits reflect the human health benefits associated with reducing exposure to PM2.5 through reductions of PM2.5 precursors, such as
NOX and SO2, as well as CO2. It is important to note that the monetized benefits do not include reduced health effects from direct exposure to
SO2 and NOX, ozone exposure, ecosystem effects or visibility impairment.
b PM benefits are shown as a range from Pope, et al. (2002) to Laden, et al. (2006). These models assume that all fine particles, regardless of
their chemical composition, are equally potent in causing premature mortality because the scientific evidence is not yet sufficient to allow differentiation of effects estimates by particle type.
c The CO emission reductions (shown in metric tonnes) have been reduced to reflect the anticipated emission increases associated with the
2
energy disbenefits. CO2-related benefits were calculated using the social cost of carbon (SCC), which is discussed further in the RIA. The net
present value of reduced CO2 emissions is calculated differently than other benefits. This table shows monetized climate benefits using the global average SCC estimate at a 3-percent discount rate because the interagency workgroup deemed the SCC at a 3-percent discount rate to be
the central value. In the RIA, we also provide the monetized CO2 benefits using discount rates of 5 percent (average), 2.5 percent (average) and
3 percent (95th percentile).
d Metric tonnes
These benefits estimates represent the
total monetized human health benefits
for populations exposed to less PM2.5 in
2017 from controls installed to reduce
air pollutants in order to meet this rule.
To estimate human health benefits of
this rule, the EPA used benefit-per-ton
factors to quantify the changes in PM2.5related health impacts and monetized
benefits based on changes in SO2 and
NOX emissions. These benefit-per-ton
factors were derived using the general
approach and methodology laid out in
Fann, Fulcher, and Hubbell (2009).13
This approach uses a model to convert
emissions of PM2.5 precursors into
changes in ambient PM2.5 levels and
another model to estimate the changes
in human health associated with that
change in air quality, which are then
divided by the emission reductions to
12 Roman, et al., 2008. Expert Judgment
Assessment of the Mortality Impact of Changes in
Ambient Fine Particulate Matter in the U.S.,
Environ. Sci. Technol., 42, 7, 2268—2274.
13 Fann, N., C.M. Fulcher, B.J. Hubbell. 2009. The
Influence of Location, Source, and Emission Type
in Estimates of the Human Health Benefits of
Reducing a Ton of Air Pollution. Air Qual Atmos
Health (2009) 2:169–176.
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
create the benefit-per-ton estimates.
However, for this rule, we use air
quality modeling data specific to the
petroleum refineries sector.14 The
primary difference between the
estimates used in this analysis and the
estimates reported in Fann, Fulcher, and
Hubbell (2009) is the air quality
modeling data utilized. While the air
quality data used in Fann, Fulcher, and
Hubbell (2009) reflects broad pollutant/
source category combinations, such as
all non-electric generating unit
stationary point sources, the air quality
modeling data used in this analysis is
sector-specific. In addition, the updated
air quality modeling data reflects more
recent emissions data (2005 rather than
2001) and has a higher spatial resolution
(12 kilometers (km) rather than 36 km
grid cells). As a result, the benefit-perton estimates presented herein better
reflect the geographic areas and
populations likely to be affected by this
sector. The benefits methodology, such
as health endpoints assessed, risk
estimates applied and valuation
techniques applied did not change.
However, these updated estimates still
have similar limitations as all nationalaverage benefit-per-ton estimates in that
they reflect the geographic distribution
of the modeled emissions, which may
not exactly match the emission
reductions in this rulemaking, and they
may not reflect local variability in
population density, meteorology,
exposure, baseline health incidence
rates or other local factors for any
specific location.
We apply these national benefit-perton estimates calculated for this sector
separately for SO2 and NOX and
multiply them by the corresponding
emission reductions. The sector-specific
modeling does not provide estimates of
the PM2.5-related benefits associated
with reducing VOC emissions, but these
unquantified benefits are generally
small compared to other PM2.5
precursors. More information regarding
the derivation of the benefit-per-ton
estimates for the petroleum refining
sector is available in the technical
support document, which is available in
the docket.
These models assume that all fine
particles, regardless of their chemical
composition, are equally potent in
causing premature mortality because the
scientific evidence is not yet sufficient
to allow differentiation of effects
estimates by particle type. The main
PM2.5 precursors affected by this rule are
14 U.S. Environmental Protection Agency. 2011.
Technical Support Document: Estimating the
Benefit per Ton of Reducing PM2.5 Precursors from
the Petroleum Refineries Sector. EPA, Research
Triangle Park, NC.
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SO2 and NOX. Even though we assume
that all fine particles have equivalent
health effects, the benefit-per-ton
estimates vary between precursors
depending on the location and
magnitude of their impact on PM2.5
levels, which drive population
exposure. For example, SO2 has a lower
benefit-per-ton estimate than direct
PM2.5 because it does not form as much
PM2.5, thus, the exposure would be
lower, and the monetized health
benefits would be lower.
It is important to note that the
magnitude of the PM2.5 benefits is
largely driven by the concentration
response function for premature
mortality. Experts have advised the EPA
to consider a variety of assumptions,
including estimates based both on
empirical (epidemiological) studies and
judgments elicited from scientific
experts, to characterize the uncertainty
in the relationship between PM2.5
concentrations and premature mortality.
We cite two key empirical studies, one
based on the American Cancer Society
cohort study 15 and the extended Six
Cities cohort study.16 In the RIA for this
final rule, which is available in the
docket, we also include benefits
estimates derived from the expert
judgments and other assumptions.
The EPA strives to use the best
available science to support our benefits
analyses. We recognize that
interpretation of the science regarding
air pollution and health is dynamic and
evolving. After reviewing the scientific
literature, we have determined that the
no-threshold model is the most
appropriate model for assessing the
mortality benefits associated with
reducing PM2.5 exposure. Consistent
with this finding, we have conformed
the previous threshold sensitivity
analysis to the current state of the PM
science by incorporating a new ‘‘Lowest
Measured Level’’ (LML) assessment in
the RIA accompanying this rule. While
an LML assessment provides some
insight into the level of uncertainty in
the estimated PM mortality benefits, the
EPA does not view the LML as a
threshold and continues to quantify PMrelated mortality impacts using a full
range of modeled air quality
concentrations.
Most of the estimated PM-related
benefits in this rule would accrue to
15 Pope, et al., 2002. Lung Cancer,
Cardiopulmonary Mortality, and Long-term
Exposure to Fine Particulate Air Pollution. Journal
of the American Medical Association 287:1132–
1141.
16 Laden, et al., 2006. Reduction in Fine
Particulate Air Pollution and Mortality. American
Journal of Respiratory and Critical Care Medicine
173: 667–672.
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populations exposed to higher levels of
PM2.5. For this analysis, policy-specific
air quality data is not available due to
time or resource limitations, thus, we
are unable to estimate the percentage of
premature mortality associated with this
specific rule’s emission reductions at
each PM2.5 level. As a surrogate measure
of mortality impacts, we provide the
percentage of the population exposed at
each PM2.5 level using the source
apportionment modeling used to
calculate the benefit-per-ton estimates
for this sector. Using the Pope, et al.
(2002) study, 77 percent of the
population is exposed to annual mean
PM2.5 levels at or above the LML of 7.5
micrograms per cubic meter (mg/m3).
Using the Laden, et al. (2006) study, 25
percent of the population is exposed
above the LML of 10 mg/m3. It is
important to emphasize that we have
high confidence in PM2.5-related effects
down to the lowest LML of the major
cohort studies. This fact is important,
because, as we model avoided
premature deaths among populations
exposed to levels of PM2.5, we have
lower confidence in levels below the
LML for each study.
Every benefit analysis examining the
potential effects of a change in
environmental protection requirements
is limited, to some extent, by data gaps,
model capabilities (such as geographic
coverage) and uncertainties in the
underlying scientific and economic
studies used to configure the benefit and
cost models. Despite these uncertainties,
we believe the benefit analysis for this
rule provides a reasonable indication of
the expected health benefits of the
rulemaking under a set of reasonable
assumptions. This analysis does not
include the type of detailed uncertainty
assessment found in the 2006 PM2.5
NAAQS RIA because we lack the
necessary air quality input and
monitoring data to run the benefits
model. In addition, we have not
conducted air quality modeling for this
rule, and using a benefit-per-ton
approach adds another important source
of uncertainty to the benefits estimates.
The 2006 PM2.5 NAAQS benefits
analysis 17 provides an indication of the
sensitivity of our results to various
assumptions.
This rule is expected to reduce CO2
emissions from the electricity sector.
The EPA has assigned a dollar value to
reductions in CO2 emissions using
recent estimates of the ‘‘social cost of
carbon’’ (SCC). The SCC is an estimate
17 U.S. Environmental Protection Agency, 2006.
Final Regulatory Impact Analysis: PM2.5 NAAQS.
Prepared by Office of Air and Radiation. October.
Available on the Internet at https://www.epa.gov/ttn/
ecas/ria.html.
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of the monetized damages associated
with an incremental increase in carbon
emissions in a given year or the per
metric ton benefit estimate relating to
decreases in CO2 emissions. It is
intended to include (but is not limited
to) changes in net agricultural
productivity, human health, property
damage from increased flood risk, and
the value of ecosystem services due to
climate change.
The SCC estimates used in this
analysis were developed through an
interagency process that included the
EPA and other executive branch
entities, and that concluded in February
2010. We first used these SCC estimates
in the benefits analysis for the final joint
EPA/DOT Rulemaking to establish
Light-Duty Vehicle Greenhouse Gas
Emission Standards and Corporate
Average Fuel Economy Standards; see
the rule’s preamble for discussion about
application of the SCC (75 FR 25324;
May 7, 2010). The SCC Technical
Support Document (SCC TSD) provides
a complete discussion of the methods
used to develop these SCC estimates.18
The interagency group selected four
SCC values for use in regulatory
analyses, which we have applied in this
analysis: $5.9, $24.3, $39, and $74.4 per
metric ton of CO2 emissions in 2016, in
2007 dollars. The first three values are
based on the average SCC from three
integrated assessment models, at
discount rates of 5, 3 and 2.5 percent,
respectively. Social cost of carbon
values at several discount rates are
included because the literature shows
that the SCC is quite sensitive to
assumptions about the discount rate,
and because no consensus exists on the
appropriate rate to use in an
intergenerational context. The fourth
value is the 95th percentile of the SCC
from all three values at a 3-percent
discount rate. It is included to represent
higher-than-expected impacts from
temperature change further out in the
extremes of the SCC distribution. Low
probability, high impact events are
incorporated into all of the SCC values
through explicit consideration of their
effects in two of the three values as well
as the use of a probability density
function for equilibrium climate
sensitivity. Treating climate sensitivity
probabilistically results in more high
temperature outcomes, which in turn
leads to higher projections of damages.
Applying the global SCC estimates
using a 3-percent discount rate, we
estimate the value of the climate related
benefits of this rule in 2017 is $49
million (2006$), as shown in Table 6.
See the RIA for more detail on the
methodology used to calculate these
benefits and additional estimates of
climate benefits using different discount
rates and the 95th percentile of the 3percent discount rate SCC. Important
limitations and uncertainties of the SCC
approach are also described in the RIA.
It should be noted that the monetized
benefits estimates provided above do
not include benefits from several
important benefit categories, including
direct exposure to SO2 and NOX, ozone
exposure, ecosystem effects and
visibility impairment. Although we do
not have sufficient information or
modeling available to provide
monetized estimates for this
rulemaking, we include a qualitative
assessment of these unquantified
benefits in the RIA for this final rule.
Although this final rule provides
refiners with some additional
compliance options and removes some
requirements, such as the long-term H2S
limit for flares, these are non-monetized
benefits of the rule.
For more information on the benefits
analysis, please refer to the RIA for this
rulemaking, which is available in the
docket.
VI. Statutory and Executive Order
Reviews
A. Executive Order 12866: Regulatory
Planning and Review and Executive
Order 13563: Improving Regulation and
Regulatory Review
Under section 3(f)(1) of Executive
Order 12866 (58 FR 51735, October 4,
1993), this action is an ‘‘economically
significant regulatory action’’ because it
is likely to have an annual effect on the
economy of $100 million or more.
Accordingly, the EPA submitted this
action to the Office of Management and
Budget (OMB) for review under
Executive Order 12866 and Executive
Order 13563 (76 FR 3821, January 21,
2011), and any changes made in
response to OMB recommendations
have been documented in the docket for
this action. In addition, the EPA
prepared a RIA of the potential costs
and benefits associated with this action.
A summary of the monetized benefits,
compliance costs and net benefits for
the final rule at discount rates of 3
percent and 7 percent is in Table 7 of
this preamble.
TABLE 7—SUMMARY OF THE MONETIZED BENEFITS, COMPLIANCE COSTS AND NET BENEFITS FOR THE FINAL PETROLEUM
REFINERIES NSPS IN 2017
[Millions of 2006 dollars] a
3-Percent discount rate
Total Monetized Benefits b ..................................
Total Compliance Costs c ...................................
Net Benefits ........................................................
7-Percent discount rate
$270 to $580 ....................................................
¥$79 ................................................................
$340 to $660 ....................................................
Non-Monetized Benefits .....................................
$240 to $530.
¥$79.
$320 to $610.
Health effects from direct exposure to SO2 and NO2.
Health effects from PM2.5 exposure from VOC
Ecosystem effects.
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Visibility impairment.
a All
estimates are for the implementation year (2017) and are rounded to two significant figures.
18 Docket ID EPA–HQ–OAR–2009–0472–114577,
Technical Support Document: Social Cost of
Carbon for Regulatory Impact Analysis Under
Executive Order 12866, Interagency Working Group
on Social Cost of Carbon, with participation by
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Council of Economic Advisers, Council on
Environmental Quality, Department of Agriculture,
Department of Commerce, Department of Energy,
Department of Transportation, Environmental
Protection Agency, National Economic Council,
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Office of Energy and Climate Change, Office of
Management and Budget, Office of Science and
Technology Policy, and Department of Treasury
(February 2010). Also available at https://epa.gov/
otaq/climate/regulations.htm.
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b The total monetized benefits reflect the human health benefits associated with reducing exposure to PM
2.5 through reductions of PM2.5 precursors such as NOX and SO2, as well as CO2 benefits. It is important to note that the monetized benefits do not include the reduced health effects from direct exposure to SO2 and NOX, ozone exposure, ecosystem effects or visibility impairment. Human health benefits are shown as a
range from Pope, et al. (2002) to Laden, et al. (2006). These models assume that all fine particles, regardless of their chemical composition, are
equally potent in causing premature mortality because the scientific evidence is not yet sufficient to allow differentiation of effects estimates by
particle type. The net present value of reduced CO2 emissions is calculated differently than other benefits. This table includes monetized climate
benefits using the global average social cost of carbon (SCC) estimated at a 3-percent discount rate because the interagency work group
deemed the SCC estimate at a 3-percent discount rate to be the central value.
c The engineering compliance costs are annualized using a 7-percent discount rate.
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To support the determination of BSER
for the June 24, 2008, final rule, we
considered a number of regulatory
options and their costs and benefits.
Those results are presented in the RIA
for the June 24, 2008, final rulemaking,
which is available in the docket. These
final rule amendments are in response
to comments received on the December
22, 2008, proposed rule amendments.
Costs and benefits associated with the
amendments in this final rule differ
from the June 24, 2008, final rule and
the December 22, 2008, proposed rule
amendments primarily as a result of
correcting the number of flares projected
to have to comply with this rule (i.e.,
400 affected flares in this rule compared
to 40 estimated in the June 24, 2008,
final rule and 150 in the December 22,
2008, proposed amendments). In
addition, the amendments in this final
rule to address comments received for
the other fuel gas combustion devices
do not affect the projected costs and
benefits from the December 22, 2008,
proposal, which also did not change
from the June 24, 2008, final rule.
Therefore, for purposes of developing
these final rule amendments, we did not
re-evaluate the suite of regulatory
options for flares and other fuel gas
combustion devices considered to
support the June 24, 2008, final rule.
However, even with the flare count
adjustment, this final rule is consistent
with Executive Order 13563 (Improving
Regulation and Regulatory Review)
because the monetized benefits of this
final rule exceed the costs. In addition,
for facilities implementing flare gas
recovery, we are reducing regulatory
burden by finalizing provisions that
would allow the owner or operator to
reduce monitoring costs and the number
of root cause analyses, corrective actions
and corresponding recordkeeping and
reporting they would need to perform.
For more information on the costbenefits analysis, please refer to the RIA
for this rulemaking, which is available
in the docket.
B. Paperwork Reduction Act
The final amendments to the
Standards of Performance for Petroleum
Refineries (40 CFR part 60, subpart J) do
not impose any new information
collection burden. The final
amendments are clarifications and
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technical corrections that do not affect
the estimated burden of the existing
rule. Therefore, we have not revised the
ICR for the existing rule. However, OMB
has previously approved the
information collection requirements
contained in the existing rule (40 CFR
part 60, subpart J) under the provisions
of the Paperwork Reduction Act, 44
U.S.C. 3501, et seq., and has assigned
OMB control number 2060–0022. The
OMB control numbers for the EPA’s
regulations are listed in 40 CFR part 9.
The OMB has approved the
information collection requirements in
the amendments to the Standards of
Performance for Petroleum Refineries
for Which Construction, Reconstruction,
or Modification Commenced After May
14, 2007 (40 CFR part 60, subpart Ja)
under the provisions of the Paperwork
Reduction Act, 44 U.S.C. 3501, et seq.,
and has assigned OMB control number
2060–0602.
The information requirements in
these final amendments add new
compliance options, provide more time
to comply with the requirements for
flares, clarify the flare management plan
requirements and clarify the flare
modification provision. Overall, these
changes are expected to reduce the costs
associated with testing, monitoring,
recording and reporting, so they will not
result in any increase in burden for the
affected facilities for which the EPA
previously estimated the burden.
However, the EPA has revised the
number of flares expected to become
subject to the rule over the first 3 years
of the ICR. Therefore, the annual burden
was estimated for the additional affected
facilities. The total burden for 40 CFR
part 60, subpart Ja can be estimated by
summing the previously approved
annual burden for OMB control number
2060–0602 (5,340 labor-hours per year
at a cost of $481,249 per year,
annualized capital costs of $2,052,000
per year, and operation and
maintenance costs of $1,117,440 per
year) and the annual burden for this
ICR, as described below.
The annual burden for this
information collection averaged over the
first 3 years of this ICR is estimated to
total 54,572 labor-hours per year at a
cost of $4,918,110 per year. The
annualized capital costs are estimated at
$11,266,000 per year and operation and
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maintenance costs are estimated at
$8,750,000 per year. We note that the
capital costs, as well as the operation
and maintenance costs, are for the
continuous monitors; these costs are
also included in the cost impacts
presented in section V.A of this
preamble. Therefore, the burden costs
associated with the continuous monitors
presented in the ICR are not additional
costs incurred by affected sources
subject to final 40 CFR part 60, subpart
Ja. Burden is defined at 5 CFR 1320.3(b).
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 are
listed in 40 CFR part 9. The EPA is
amending the table in 40 CFR part 9 of
currently approved ICR control numbers
for various regulations to list regulatory
citations for the information
requirements contained in this final
rule. This amendment updates the table
to list the information collection
requirements being promulgated here as
amendments to the NSPS for petroleum
refineries.
The EPA will continue to present
OMB control numbers in a consolidated
table format to be codified in 40 CFR
part 9 of the agency’s regulations and in
each CFR volume containing the EPA
regulations. The table lists the section
numbers with reporting and
recordkeeping requirements and the
current OMB control numbers. This
listing of the OMB control numbers and
their subsequent codification in the CFR
satisfy the requirements of the
Paperwork Reduction Act (44 U.S.C.
3501, et seq.) and OMB’s implementing
regulations at 5 CFR part 1320.
C. Regulatory Flexibility Act
The Regulatory Flexibility Act
generally requires an agency to prepare
a regulatory flexibility analysis of any
rule subject to notice and comment
rulemaking requirements under the
Administrative Procedure Act or any
other statute unless the agency certifies
that the rule would not have a
significant economic impact on a
substantial number of small entities.
Small entities include small businesses,
small organizations and small
governmental jurisdictions.
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For purposes of assessing the impact
of this final action on small entities,
small entity is defined as: (1) A small
business whose parent company has no
more than 1,500 employees, that is
primarily engaged in refining crude
petroleum into refined petroleum as
defined by NAICS code 32411 (as
defined by Small Business
Administration size standards); (2) a
small governmental jurisdiction that is a
government of a city, county, town,
school district or special district with a
population of less than 50,000; and (3)
a small organization that is any not-forprofit enterprise which is independently
owned and operated and is not
dominant in its field.
While we estimated the natural gas
recovery offsets or credit at a national
level and believe that larger firms are
more likely to offset natural gas
purchases, the revenues from natural
gas recovery offsets might mask
disproportionate impacts on small
refiners. To better identify
disproportionate impacts, we examined
the potential impacts on refiners based
on a scenario where no firms adopt flare
gas recovery systems and comply with
the NSPS through flare monitoring and
flare management and root cause
analysis actions. The incremental
compliance costs imposed on small
refineries are not estimated to create
significant impacts on a cost-to-sales
ratio basis at the firm level. Therefore,
no adverse economic impacts are
expected for any small or large entity.
After considering the economic
impacts of these final amendments on
small entities, I certify that this action
will not have a significant economic
impact on a substantial number of small
entities. The small entities directly
regulated by these final amendments are
small petroleum refineries. We have
determined that 31 small refiners, or 55
percent of total refiners, will experience
an impact of between less than 0.01
percent up to 0.63 percent of revenues.
D. Unfunded Mandates Reform Act
This rule does not contain a federal
mandate that may result in expenditures
of $100 million or more for state, local
and tribal governments, in the aggregate,
or the private sector in any one year.
The costs of the final amendments
would not increase costs associated
with the final rule. Thus, this rule is not
subject to the requirements of sections
202 or 205 of the UMRA.
This rule is also not subject to the
requirements of section 203 of UMRA
because it contains no regulatory
requirements that might significantly or
uniquely affect small governments. The
final amendments contain no
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requirements that apply to such
governments and impose no obligations
upon them.
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, as specified in
Executive Order 13132. This action does
not modify existing responsibilities or
create new responsibilities among EPA
Regional offices, states or local
enforcement agencies. Thus, Executive
Order 13132 does not apply to this
action.
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
This action does not have tribal
implications, as specified in Executive
Order 13175 (65 FR 67249, November 9,
2000). The final amendments impose no
requirements on tribal governments.
Thus, Executive Order 13175 does not
apply to this action.
G. Executive Order 13045: Protection of
Children From Environmental Health
Risks and Safety Risks
The EPA interprets Executive Order
13045 (62 FR 19885, April 23, 1997) as
applying to those regulatory actions that
concern health or safety risks, such that
the analysis required under section 5–
501 of the Executive Order has the
potential to influence the regulation.
This action is not subject to Executive
Order 13045 because it is based solely
on technology performance.
H. Executive Order 13211: Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution, or Use
This action is not a ‘‘significant
energy action’’ as defined in Executive
Order 13211 (66 FR 28355, May 22,
2001), because it is not likely to have a
significant adverse effect on the supply,
distribution or use of energy. The final
amendments would not increase the
level of energy consumption required
for the final rule and may decrease
energy requirements.
I. National Technology Transfer and
Advancement Act
Section 12(d) of the National
Technology Transfer and Advancement
Act of 1995 (NTTAA), Public Law 104–
113, 12(d) (15 U.S.C. 272 note) directs
the EPA to use voluntary consensus
standards (VCS) in its regulatory
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activities, unless to do so would be
inconsistent with applicable law or
otherwise impractical. VCS are
technical standards (e.g., materials
specifications, test methods, sampling
procedures and business practices) that
are developed or adopted by VCS
bodies. NTTAA directs the EPA to
provide Congress, through OMB,
explanations when the agency decides
not to use available and applicable VCS.
This rulemaking involves technical
standards. The EPA has decided to use
the following VCS for determining the
higher heating value of fuel fed to
process heaters: ASTM D240–02
(Reapproved 2007), Standard Test
Method for Heat of Combustion of
Liquid Hydrocarbon Fuels by Bomb
Calorimeter; ASTM D1826–94
(Reapproved 2003), Standard Test
Method for Calorific (Heating) Value of
Gases in Natural Gas Range by
Continuous Recording Calorimeter;
ASTM D3588–98 (Reapproved 2003),
Standard Practice for Calculating Heat
Value, Compressibility Factor, and
Relative Density of Gaseous Fuels;
ASTM D4809–06, Standard Test
Method for Heat of Combustion of
Liquid Hydrocarbon Fuels by Bomb
Calorimeter (Precision Method); ASTM
D4891–89 (Reapproved 2006), Standard
Test Method for Heating Value of Gases
in Natural Gas Range by Stoichiometric
Combustion; ASTM D1945–03
(Reapproved 2010), Standard Method
for Analysis of Natural Gas by Gas
Chromatography; and ASTM D1946–90
(Reapproved 2006), Standard Method
for Analysis of Reformed Gas by Gas
Chromatography.
The EPA has decided to use the
following VCS as acceptable alternatives
to EPA Methods 2, 2A, 2B, 2C or 2D for
conducting relative accuracy
evaluations of fuel gas flow monitors:
American Society of Mechanical
Engineers (ASME) MFC–3M–2004,
Measurement of Fluid Flow in Pipes
Using Orifice, Nozzle, and Venturi;
ANSI/ASME MFC–4M–1986
(Reaffirmed 2008), Measurement of Gas
Flow by Turbine Meters; ASME MFC–
6M–1998 (Reaffirmed 2005),
Measurement of Fluid Flow in Pipes
Using Vortex Flowmeters; ASME/ANSI
MFC–7M–1987 (Reaffirmed 2006),
Measurement of Gas Flow by Means of
Critical Flow Venturi Nozzles; ASME
MFC–11M–2006, Measurement of Fluid
Flow by Means of Coriolis Mass
Flowmeters; ASME MFC–14M–2003,
Measurement of Fluid Flow Using Small
Bore Precision Orifice Meters; and
ASME MFC–18M–2001, Measurement
of Fluid Flow Using Variable Area
Meters.
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The EPA has also decided to use the
following VCS as acceptable alternatives
to EPA Methods 2, 2A, 2B, 2C or 2D for
conducting relative accuracy
evaluations of fuel oil flow monitors:
ANSI/ASME MFC–5M–1985
(Reaffirmed 2006), Measurement of
Liquid Flow in Closed Conduits Using
Transit-Time Ultrasonic Flowmeters;
ASME/ANSI MFC–9M–1988
(Reaffirmed 2006), Measurement of
Liquid Flow in Closed Conduits by
Weighing Method; ASME MFC–16–
2007, Measurement of Liquid Flow in
Closed Conduits with Electromagnetic
Flowmeters; ASME MFC–22–2007,
Measurement of Liquid by Turbine
Flowmeters; and ISO 8316:
Measurement of Liquid Flow in Closed
Conduits—Method by Collection of the
Liquid in a Volumetric Tank (1987–10–
01)—First Edition.
The EPA has decided to use the
following VCS as acceptable alternatives
to EPA Method 15A and 16A for
conducting relative accuracy
evaluations of monitors for reduced
sulfur compounds, total sulfur
compounds, and H2S: ANSI/ASME PTC
19.10–1981, Flue and Exhaust Gas
Analyses. The EPA has decided to use
the following VCS as acceptable
alternatives to EPA Method 16A for
analysis of total sulfur samples: ASTM
D4468–85 (Reapproved 2006), Standard
Test Method for Total Sulfur in Gaseous
Fuels by Hydrogenolysis and
Rateometric Colorimetry; and ASTM
D5504–08, Standard Test Method for
Determination of Sulfur Compounds in
Natural Gas and Gaseous Fuels by Gas
Chromatography and
Chemiluminescence.
The EPA has decided to use the
following VCS as acceptable alternatives
to EPA Method 18 for relative accuracy
evaluations of gas composition
analyzers for gas-fired process heaters:
ASTM D1945–03 (Reapproved 2010),
Standard Method for Analysis of
Natural Gas by Gas Chromatography;
ASTM D1946–90 (Reapproved 2006),
Standard Method for Analysis of
Reformed Gas by Gas Chromatography;
ASTM UOP539–97, Refinery Gas
Analysis by Gas Chromatography; and
ASTM D6420–99 (Reapproved 2004),
Standard Test Method for
Determination of Gaseous Organic
Compounds by Direct Interface Gas
Chromatography-Mass Spectrometry.
However, ASTM D6420–99 is a suitable
alternative to EPA Method 18 only
where:
(1) The target compound(s) are those
listed in Section 1.1 of ASTM D6420–
99, and
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(2) The target concentration is
between 150 parts per billion by volume
and 100 ppmv.
For target compound(s) not listed in
Section 1.1 of ASTM D6420–99, but
potentially detected by mass
spectrometry, the regulation specifies
that the additional system continuing
calibration check after each run, as
detailed in Section 10.5.3 of the ASTM
method, must be followed, met,
documented and submitted with the
data report even if there is no moisture
condenser used or the compound is not
considered water soluble. For target
compound(s) not listed in Section 1.1 of
ASTM D6420–99 and not amenable to
detection by mass spectrometry, ASTM
D6420–99 does not apply.
These above-listed VCS are
incorporated by reference (see 40 CFR
60.17).
The EPA has also decided to use
American Gas Association Report No. 3:
Orifice Metering for Natural Gas and
Other Related Hydrocarbon Fluids, Part
1: General Equations and Uncertainty
Guidelines (1990), American Gas
Association Report No. 3: Orifice
Metering for Natural Gas and Other
Related Hydrocarbon Fluids, Part 2:
Specification and Installation
Requirements (2000), American Gas
Association Report No. 11:
Measurement of Natural Gas by Coriolis
Meter (2003), American Gas Association
Transmission Measurement Committee
Report No. 7, Measurement of Natural
Gas by Turbine Meters (Revised
February 2006) and API’s Manual of
Petroleum Measurement Standards,
Chapter 22—Testing Protocol, Section
2—Differential Pressure Flow
Measurement Devices, First Edition,
August 2005, for conducting relative
accuracy evaluations of fuel gas flow
monitors; Gas Processors Association
(GPA) Standard 2261–00, Analysis for
Natural Gas and Similar Gaseous
Mixtures by Gas Chromatography
(2000), for relative accuracy evaluations
of gas composition analyzers for gasfired process heaters; and GPA 2172–09,
Calculation of Gross Heating Value,
Relative Density, Compressibility and
Theoretical Hydrocarbon Liquid Content
for Natural Gas Mixtures for Custody
Transfer, for determining the higher
heating value of fuel fed to process
heaters. These methods are also
incorporated by reference (see 40 CFR
60.17).
While the agency has identified five
VCS as being potentially applicable to
this rule, we have decided not to use
these VCS in this rulemaking. The use
of these VCS would be impractical
because they do not meet the objectives
of the standards cited in this rule. See
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56461
the docket for this rule for the reasons
for these determinations.
Under 40 CFR 60.13(i) of the NSPS
General Provisions, a source may apply
to the EPA for permission to use
alternative test methods or alternative
monitoring requirements in place of any
required testing methods, performance
specifications or procedures in the final
rule and amendments.
J. Executive Order 12898: Federal
Actions To Address Environmental
Justice in Minority Populations and
Low-Income Populations
Executive Order 12898 (59 FR 7629,
February 16, 1994) establishes federal
executive policy on environmental
justice. Its main provision directs
federal agencies, to the greatest extent
practicable and permitted by law, to
make environmental justice part of their
mission by identifying and addressing,
as appropriate, disproportionately high
and adverse human health or
environmental effects of their programs,
policies and activities on minority
populations and low-income
populations in the United States.
The EPA has determined that this
final rule will not have
disproportionately high and adverse
human health or environmental effects
on minority or low-income populations
because it does not affect the level of
protection provided to human health or
the environment. The final amendments
are either clarifications or compliance
alternatives which will neither increase
or decrease environmental protection.
K. Congressional Review Act
The Congressional Review Act, 5
U.S.C. 801, et seq., as added by the
Small Business Regulatory Enforcement
Fairness Act of 1996, generally provides
that before a rule may take effect the
agency promulgating the rule must
submit a rule report, which includes a
copy of the rule, to each House of
Congress and to the Comptroller General
of the United States. The EPA will
submit a report containing these final
rules and other required information to
the United States Senate, the United
States House of Representatives and the
Comptroller General of the United
States prior to publication of the final
rules in the Federal Register. A major
rule cannot take effect until 60 days
after it is published in the Federal
Register. This action is a ‘‘major rule’’
as defined by 5 U.S.C. 804(2). This final
rule will be effective on November 13,
2012.
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
List of Subjects
PART 60—[AMENDED]
40 CFR Part 9
■
Environmental protection, Reporting
and recordkeeping requirements.
3. The authority citation for part 60
continues to read as follows:
Authority: 42 U.S.C. 7401, et seq.
40 CFR Part 60
Subpart A—[AMENDED]
Environmental protection,
Administrative practice and procedure,
Air pollution control, Incorporation by
reference, Intergovernmental relations,
Reporting and recordkeeping
requirements.
■
■
Dated: June 1, 2012.
Lisa P. Jackson,
Administrator.
For the reasons stated in the
preamble, title 40, chapter I, of the Code
of Federal Regulations is amended as
follows:
1. The authority citation for part 9
continues to read as follows:
■
Authority: 7 U.S.C. 135, et seq., 136–136y;
15 U.S.C. 2001, 2003, 2005, 2006, 2601–2671;
21 U.S.C. 331j, 346a, 348; 31 U.S.C. 9701; 33
U.S.C. 1251, et seq., 1311, 1313d, 1314, 1318,
1321, 1326, 1330, 1342, 1344, 1345(d) and
(e), 1361; E.O. 11735, 38 FR 21243, 3 CFR,
1971–1975 Comp. p. 973; 42 U.S.C. 241,
242b, 243, 246, 300f, 300g, 300g–1, 300g–2,
300g–3, 300g–4, 300g–5, 300g–6, 300j–1,
300j–2, 300j–3, 300j–4, 300j–9, 1857, et seq.,
6901–6992k, 7401–7671q, 7542, 9601–9657,
11023, 11048.
2. The table in Section 9.1 is amended
by adding an entry in numerical order
for 60.103a–60.108a under the heading
‘‘Standards of Performance for New
Stationary Sources’’ to read as follows:
■
§ 9.1 OMB Approvals under the Paperwork
Reduction Act.
*
*
*
*
OMB control
No.
40 CFR citation
*
*
*
*
*
Standards of Performance for New
Stationary Sources 1
*
*
*
*
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60.103a–60.108a ..................
*
*
*
*
2060–0602
*
1 The
*
ICRs referenced in this section of the
table encompass the applicable general provisions contained in 40 CFR part 60, subpart A,
which are not independent information collection requirements.
*
*
*
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*
*
20:34 Sep 11, 2012
§ 60.17
Incorporations by reference.
*
PART 9—[AMENDED]
*
4. Section 60.17 is amended by:
a. Revising paragraphs (a)(84), (a)(95),
(a)(96), (a)(97), and (a)(98);
■ b. Adding paragraphs (a)(100) through
(a)(108);
■ c. Adding paragraph (c)(2);
■ d. Revising paragraph (h)(4) and
adding paragraphs (h)(5) through
(h)(15);
■ e. Adding paragraphs (m)(2) and
(m)(3); and
■ f. Adding paragraphs (p) and (q) to
read as follows:
Jkt 226001
*
*
*
*
(a) * * *
(84) ASTM D6420–99 (Reapproved
2004), Standard Test Method for
Determination of Gaseous Organic
Compounds by Direct Interface Gas
Chromatography-Mass Spectrometry,
(Approved October 1, 2004), IBR
approved for § 60.107a(d) of subpart Ja
and table 2 of subpart JJJJ of this part.
*
*
*
*
*
(95) ASTM D3588–98 (Reapproved
2003), Standard Practice for Calculating
Heat Value, Compressibility Factor, and
Relative Density of Gaseous Fuels,
(Approved May 10, 2003), IBR approved
for §§ 60.107a(d) and 60.5413(d).
(96) ASTM D4891–89 (Reapproved
2006), Standard Test Method for
Heating Value of Gases in Natural Gas
Range by Stoichiometric Combustion,
(Approved June 1, 2006), IBR approved
for §§ 60.107a(d) and 60.5413(d).
(97) ASTM D1945–03 (Reapproved
2010), Standard Method for Analysis of
Natural Gas by Gas Chromatography,
(Approved January 1, 2010), IBR
approved for §§ 60.107a(d) and
60.5413(d).
(98) ASTM D5504–08, Standard Test
Method for Determination of Sulfur
Compounds in Natural Gas and Gaseous
Fuels by Gas Chromatography and
Chemiluminescence, (Approved June
15, 2008), IBR approved for
§§ 60.107a(e) and 60.5413(d).
*
*
*
*
*
(100) ASTM D4468–85 (Reapproved
2006), Standard Test Method for Total
Sulfur in Gaseous Fuels by
Hydrogenolysis and Rateometric
Colorimetry (Approved June 1, 2006),
IBR approved for § 60.107a(e).
(101) ASTM D240–02 (Reapproved
2007), Standard Test Method for Heat of
Combustion of Liquid Hydrocarbon
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Fuels by Bomb Calorimeter, (Approved
May 1, 2007), IBR approved for
§ 60.107a(d).
(102) ASTM D1826–94 (Reapproved
2003), Standard Test Method for
Calorific (Heating) Value of Gases in
Natural Gas Range by Continuous
Recording Calorimeter, (Approved May
10, 2003), IBR approved for
§ 60.107a(d).
(103) ASTM D1946–90 (Reapproved
2006), Standard Method for Analysis of
Reformed Gas by Gas Chromatography,
(Approved June 1, 2006), IBR approved
for § 60.107a(d).
(104) ASTM D4809–06, Standard Test
Method for Heat of Combustion of
Liquid Hydrocarbon Fuels by Bomb
Calorimeter (Precision Method),
(Approved December 1, 2006), IBR
approved for § 60.107a(d).
(105) ASTM UOP539–97, Refinery
Gas Analysis by Gas Chromatography,
(Copyright 1997), IBR approved for
§ 60.107a(d).
(106) ASTM D3699–08, Standard
Specification for Kerosine, including
Appendix X1, (Approved September 1,
2008), IBR approved for §§ 60.41b of
subpart Db and 60.41c of subpart Dc of
this part.
(107) ASTM D6751–11b, Standard
Specification for Biodiesel Fuel Blend
Stock (B100) for Middle Distillate Fuels,
including Appendices X1 through X3,
(Approved July 15, 2011), IBR approved
for §§ 60.41b of subpart Db and 60.41c
of subpart Dc of this part.
(108) ASTM D7467–10, Standard
Specification for Diesel Fuel Oil,
Biodiesel Blend (B6 to B20), including
Appendices X1 through X3, (Approved
August 1, 2010), IBR approved for
§§ 60.41b of subpart Db and 60.41c of
subpart Dc of this part.
*
*
*
*
*
(c) * * *
(2) American Petroleum Institute
(API) Manual of Petroleum
Measurement Standards, Chapter 22Testing Protocol, Section 2-Differential
Pressure Flow Measurement Devices,
First Edition, August 2005, IBR
approved for § 60.107a(d) of subpart Ja
of this part.
*
*
*
*
*
(h) * * *
(4) ANSI/ASME PTC 19.10–1981,
Flue and Exhaust Gas Analyses [Part 10,
Instruments and Apparatus], (Issued
August 31, 1981), IBR approved for
§ 60.56c(b), § 60.63(f), § 60.106(e),
§ 60.104a(d), (h), (i), and (j),
§ 60.105a(d), (f), and (g), § 60.106a(a),
§ 60.107a(a), (c), and (e), tables 1 and 3
of subpart EEEE, tables 2 and 4 of
subpart FFFF, table 2 of subpart JJJJ,
§§ 60.4415(a), 60.2145(s), 60.2145(t),
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60.2710(s), 60.2710(t), 60.2710(w),
60.2730(q), 60.4900(b), 60.5220(b),
tables 1 and 2 to subpart LLLL, tables 2
and 3 to subpart MMMM, §§ 60.5406(c)
and 60.5413(b).
(5) ASME MFC–3M–2004,
Measurement of Fluid Flow in Pipes
Using Orifice, Nozzle, and Venturi, IBR
approved for § 60.107a(d) of subpart Ja
of this part.
(6) ANSI/ASME MFC–4M–1986
(Reaffirmed 2008), Measurement of Gas
Flow by Turbine Meters, IBR approved
for § 60.107a(d) of subpart Ja of this part.
(7) ANSI/ASME–MFC–5M–1985
(Reaffirmed 2006), Measurement of
Liquid Flow in Closed Conduits Using
Transit-Time Ultrasonic Flowmeters,
IBR approved for § 60.107a(d) of subpart
Ja of this part.
(8) ASME MFC–6M–1998 (Reaffirmed
2005), Measurement of Fluid Flow in
Pipes Using Vortex Flowmeters, IBR
approved for § 60.107a(d) of subpart Ja
of this part.
(9) ASME/ANSI MFC–7M–1987
(Reaffirmed 2006), Measurement of Gas
Flow by Means of Critical Flow Venturi
Nozzles, IBR approved for § 60.107a(d)
of subpart Ja of this part.
(10) ASME/ANSI MFC–9M–1988
(Reaffirmed 2006), Measurement of
Liquid Flow in Closed Conduits by
Weighing Method, IBR approved for
§ 60.107a(d) of subpart Ja of this part.
(11) ASME MFC–11M–2006,
Measurement of Fluid Flow by Means of
Coriolis Mass Flowmeters, IBR
approved for § 60.107a(d) of subpart Ja
of this part.
(12) ASME MFC–14M–2003,
Measurement of Fluid Flow Using Small
Bore Precision Orifice Meters, IBR
approved for § 60.107a(d) of subpart Ja
of this part.
(13) ASME MFC–16–2007,
Measurement of Liquid Flow in Closed
Conduits with Electromagnetic
Flowmeters, IBR approved for
§ 60.107a(d) of subpart Ja of this part.
(14) ASME MFC–18M–2001,
Measurement of Fluid Flow Using
Variable Area Meters, IBR approved for
§ 60.107a(d) of subpart Ja of this part.
(15) ASME MFC–22–2007,
Measurement of Liquid by Turbine
Flowmeters, IBR approved for
§ 60.107a(d) of subpart Ja of this part.
*
*
*
*
*
(m) * * *
(2) Gas Processors Association
Standard 2172–09, Calculation of Gross
Heating Value, Relative Density,
Compressibility and Theoretical
Hydrocarbon Liquid Content for Natural
Gas Mixtures for Custody Transfer
(2009), IBR approved for § 60.107a(d) of
subpart Ja of this part.
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Jkt 226001
(3) Gas Processors Association
Standard 2261–00, Analysis for Natural
Gas and Similar Gaseous Mixtures by
Gas Chromatography (2000), IBR
approved for § 60.107a(d) of subpart Ja
of this part.
*
*
*
*
*
(p) The following American Gas
Association material is available for
purchase from the following address: ILI
Infodisk, 610 Winters Avenue, Paramus,
New Jersey 07652:
(1) American Gas Association Report
No. 3: Orifice Metering for Natural Gas
and Other Related Hydrocarbon Fluids,
Part 1: General Equations and
Uncertainty Guidelines (1990), IBR
approved for § 60.107a(d) of subpart Ja
of this part.
(2) American Gas Association Report
No. 3: Orifice Metering for Natural Gas
and Other Related Hydrocarbon Fluids,
Part 2: Specification and Installation
Requirements (2000), IBR approved for
§ 60.107a(d) of subpart Ja of this part.
(3) American Gas Association Report
No. 11: Measurement of Natural Gas by
Coriolis Meter (2003), IBR approved for
§ 60.107a(d) of subpart Ja of this part.
(4) American Gas Association
Transmission Measurement Committee
Report No. 7: Measurement of Gas by
Turbine Meters (Revised February
2006), IBR approved for § 60.107a(d) of
subpart Ja of this part.
(q) The following material is available
for purchase from the International
Standards Organization (ISO), 1, ch. de
la Voie-Creuse, Case postale 56, CH–
1211 Geneva 20, Switzerland, +41 22
749 01 11, https://www.iso.org/iso/
home.htm.
(1) ISO 8316: Measurement of Liquid
Flow in Closed Conduits—Method by
Collection of the Liquid in a Volumetric
Tank (1987–10–01)—First Edition, IBR
approved for § 60.107a(d) of subpart Ja
of this part.
(2) [Reserved]
5. Section 60.100 is amended by:
a. Revising paragraph (b);
b. Redesignating paragraph (e) as (f);
and
■ c. Adding a new paragraph (e) to read
as follows:
■
■
■
§ 60.100 Applicability, designation of
affected facility, and reconstruction.
*
*
*
*
(b) Any fluid catalytic cracking unit
catalyst regenerator or fuel gas
combustion device under paragraph (a)
of this section other than a flare which
commences construction, reconstruction
or modification after June 11, 1973, and
on or before May 14, 2007, or any fuel
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gas combustion device under paragraph
(a) of this section that is also a flare
which commences construction,
reconstruction or modification after
June 11, 1973, and on or before June 24,
2008, or any Claus sulfur recovery plant
under paragraph (a) of this section
which commences construction,
reconstruction or modification after
October 4, 1976, and on or before May
14, 2007, is subject to the requirements
of this subpart except as provided under
paragraphs (c) through (e) of this
section.
*
*
*
*
*
(e) Owners or operators may choose to
comply with the applicable provisions
of subpart Ja of this part to satisfy the
requirements of this subpart for an
affected facility.
*
*
*
*
*
6. Section 60.101 is amended by
revising paragraph (d) to read as
follows:
■
§ 60.101
Definitions.
*
*
*
*
*
(d) Fuel gas means any gas which is
generated at a petroleum refinery and
which is combusted. Fuel gas includes
natural gas when the natural gas is
combined and combusted in any
proportion with a gas generated at a
refinery. Fuel gas does not include gases
generated by catalytic cracking unit
catalyst regenerators and fluid coking
burners. Fuel gas does not include
vapors that are collected and combusted
in a thermal oxidizer or flare installed
to control emissions from wastewater
treatment units or marine tank vessel
loading operations.
*
*
*
*
*
■ 7. Section 60.106 is amended by
revising paragraph (c)(1) to read as
follows:
§ 60.106
Test methods and procedures.
*
Subpart J—[AMENDED]
*
56463
*
*
*
*
(c) * * *
(1) The allowable emission rate (Es) of
PM shall be computed for each run
using the following equation:
Es = F + A (H/Rc)
Where:
Es = Emission rate of PM allowed, kg/Mg (lb/
ton) of coke burn-off in catalyst
regenerator.
F = Emission standard, 1.0 kg/Mg (2.0 lb/ton)
of coke burn-off in catalyst regenerator.
A = Allowable incremental rate of PM
emissions, 43 g/GJ (0.10 lb/million Btu).
H = Heat input rate from solid or liquid fossil
fuel, GJ/hr (million Btu/hr).
Rc = Coke burn-off rate, Mg coke/hr (ton
coke/hr).
*
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
Subpart Ja—[AMENDED]
7. In § 60.100a, lift the stay on
paragraph (c) published December 22,
2008 (73 FR 78552).
■ 8. Section 60.100a is amended by:
■ a. Revising paragraph (a);
■ b. Revising paragraph (b);
■ c. Revising paragraph (c) introductory
text and paragraph (c)(1); and
■ d. Revising paragraph (d).
The revisions read as follows:
■
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§ 60.100a Applicability, designation of
affected facility, and reconstruction.
(a) The provisions of this subpart
apply to the following affected facilities
in petroleum refineries: fluid catalytic
cracking units (FCCU), fluid coking
units (FCU), delayed coking units, fuel
gas combustion devices (including
process heaters), flares and sulfur
recovery plants. The sulfur recovery
plant need not be physically located
within the boundaries of a petroleum
refinery to be an affected facility,
provided it processes gases produced
within a petroleum refinery.
(b) Except for flares and delayed
coking units, the provisions of this
subpart apply only to affected facilities
under paragraph (a) of this section
which commence construction,
modification or reconstruction after May
14, 2007. For flares, the provisions of
this subpart apply only to flares which
commence construction, modification or
reconstruction after June 24, 2008. For
the purposes of this subpart, a
modification to a flare commences when
a project that includes any of the
activities in paragraphs (c)(1) or (2) of
this section is commenced. For delayed
coking units, the provisions of this
subpart apply to delayed coking units
that commence construction,
reconstruction or modification on the
earliest of the following dates:
(1) May 14, 2007, for such activities
that involve a ‘‘delayed coking unit’’
defined as follows: one or more refinery
process units in which high molecular
weight petroleum derivatives are
thermally cracked and petroleum coke
is produced in a series of closed, batch
system reactors;
(2) December 22, 2008, for such
activities that involve a ‘‘delayed coking
unit’’ defined as follows: a refinery
process unit in which high molecular
weight petroleum derivatives are
thermally cracked and petroleum coke
is produced in a series of closed, batch
system reactors. A delayed coking unit
consists of the coke drums and
associated fractionator;
(3) September 12, 2012, for such
activities that involve a ‘‘delayed coking
unit’’ as defined in § 60.101a.
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(c) For all affected facilities other than
flares, the provisions in § 60.14
regarding modification apply. As
provided in § 60.14(f), the special
provisions set forth under this subpart
shall supersede the provisions in § 60.14
with respect to flares. For the purposes
of this subpart, a modification to a flare
occurs as provided in paragraphs (c)(1)
or (2) of this section.
(1) Any new piping from a refinery
process unit, including ancillary
equipment, or a fuel gas system is
physically connected to the flare (e.g.,
for direct emergency relief or some form
of continuous or intermittent venting).
However, the connections described in
paragraphs (c)(1)(i) through (vii) of this
section are not considered modifications
of a flare.
(i) Connections made to install
monitoring systems to the flare.
(ii) Connections made to install a flare
gas recovery system or connections
made to upgrade or enhance
components of a flare gas recovery
system (e.g., addition of compressors or
recycle lines).
(iii) Connections made to replace or
upgrade existing pressure relief or safety
valves, provided the new pressure relief
or safety valve has a set point opening
pressure no lower and an internal
diameter no greater than the existing
equipment being replaced or upgraded.
(iv) Connections made for flare gas
sulfur removal.
(v) Connections made to install backup (redundant) equipment associated
with the flare (such as a back-up
compressor) that does not increase the
capacity of the flare.
(vi) Replacing piping or moving an
existing connection from a refinery
process unit to a new location in the
same flare, provided the new pipe
diameter is less than or equal to the
diameter of the pipe/connection being
replaced/moved.
(vii) Connections that interconnect
two or more flares.
*
*
*
*
*
(d) For purposes of this subpart,
under § 60.15, the ‘‘fixed capital cost of
the new components’’ includes the fixed
capital cost of all depreciable
components which are or will be
replaced pursuant to all continuous
programs of component replacement
which are commenced within any 2year period following the relevant
applicability date specified in paragraph
(b) of this section.
■ 9. In § 60.101a, lift the stay on the
definition of ‘‘flare’’ published
December 22, 2008 (73 FR 78552).
■ 10. Section 60.101a is amended by:
■ a. Revising the introductory text;
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b. Adding, in alphabetical order,
definitions of ‘‘Air preheat,’’ ‘‘Ancillary
equipment,’’ ‘‘Cascaded flare system,’’
‘‘Co-fired process heater,’’ ‘‘Corrective
action,’’ ‘‘Corrective action analysis,’’
‘‘Emergency flare,’’ ‘‘Flare gas header
system,’’ ‘‘Flare gas recovery system,’’
‘‘Forced draft process heater,’’ ‘‘Natural
draft process heater,’’ ‘‘Non-emergency
flare,’’ ‘‘Primary flare,’’ ‘‘Purge gas,’’
‘‘Root cause analysis,’’ ‘‘Secondary
flare,’’ and ‘‘Sweep gas’’; and
■ c. Revising the definitions of ‘‘Delayed
coking unit,’’ ‘‘Flare,’’ ‘‘Flexicoking
unit,’’ ‘‘Fluid coking unit,’’ ‘‘Fuel gas,’’
‘‘Fuel gas combustion device,’’
‘‘Petroleum refinery,’’ ‘‘Process upset
gas’’ and ‘‘Sulfur recovery plant’’
The revisions and additions read as
follows:
■
§ 60.101a
Definitions.
Terms used in this subpart are
defined in the Clean Air Act (CAA), in
§ 60.2 and in this section.
Air preheat means a device used to
heat the air supplied to a process heater
generally by use of a heat exchanger to
recover the sensible heat of exhaust gas
from the process heater.
Ancillary equipment means
equipment used in conjunction with or
that serve a refinery process unit.
Ancillary equipment includes, but is not
limited to, storage tanks, product
loading operations, wastewater
treatment systems, steam- or electricityproducing units (including coke
gasification units), pressure relief
valves, pumps, sampling vents and
continuous analyzer vents.
Cascaded flare system means a series
of flares connected to one flare gas
header system arranged with increasing
pressure set points so that discharges
will be initially directed to the first flare
in the series (i.e., the primary flare). If
the discharge pressure exceeds a set
point at which the flow to the primary
flare would exceed the primary flare’s
capacity, flow will be diverted to the
second flare in the series. Similarly,
flow would be diverted to a third (or
fourth) flare if the pressure in the flare
gas header system exceeds a threshold
where the flow to the first two (or three)
flares would exceed their capacities.
Co-fired process heater means a
process heater that employs burners that
are designed to be supplied by both
gaseous and liquid fuels on a routine
basis. Process heaters that have gas
burners with emergency oil back-up
burners are not considered co-fired
process heaters.
*
*
*
*
*
Corrective action means the design,
operation and maintenance changes that
one takes consistent with good
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engineering practice to reduce or
eliminate the likelihood of the
recurrence of the primary cause and any
other contributing cause(s) of an event
identified by a root cause analysis as
having resulted in a discharge of gases
to an affected flare in excess of specified
thresholds.
Corrective action analysis means a
description of all reasonable interim and
long-term measures, if any, that are
available, and an explanation of why the
selected corrective action(s) is/are the
best alternative(s), including, but not
limited to, considerations of cost
effectiveness, technical feasibility,
safety and secondary impacts.
Delayed coking unit means a refinery
process unit in which high molecular
weight petroleum derivatives are
thermally cracked and petroleum coke
is produced in a series of closed, batch
system reactors. A delayed coking unit
includes, but is not limited to, all of the
coke drums associated with a single
fractionator; the fractionator, including
the bottoms receiver and the overhead
condenser; the coke drum cutting water
and quench system, including the jet
pump and coker quench water tank;
process piping and associated
equipment such as pumps, valves and
connectors; and the coke drum
blowdown recovery compressor system.
Emergency flare means a flare that
combusts gas exclusively released as a
result of malfunctions (and not startup,
shutdown, routine operations or any
other cause) on four or fewer occasions
in a rolling 365-day period. For
purposes of this rule, a flare cannot be
categorized as an emergency flare unless
it maintains a water seal.
Flare means a combustion device that
uses an uncontrolled volume of air to
burn gases. The flare includes the
foundation, flare tip, structural support,
burner, igniter, flare controls, including
air injection or steam injection systems,
flame arrestors and the flare gas header
system. In the case of an interconnected
flare gas header system, the flare
includes each individual flare serviced
by the interconnected flare gas header
system and the interconnected flare gas
header system.
Flare gas header system means all
piping and knockout pots, including
those in a subheader system, used to
collect and transport gas to a flare either
from a process unit or a pressure relief
valve from the fuel gas system,
regardless of whether or not a flare gas
recovery system draws gas from the flare
gas header system. The flare gas header
system includes piping inside the
battery limit of a process unit if the
purpose of the piping is to transport gas
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to a flare or knockout pot that is part of
the flare.
Flare gas recovery system means a
system of one or more compressors,
piping and the associated water seal,
rupture disk or similar device used to
divert gas from the flare and direct the
gas to the fuel gas system or to a fuel
gas combustion device.
Flexicoking unit means a refinery
process unit in which high molecular
weight petroleum derivatives are
thermally cracked and petroleum coke
is continuously produced and then
gasified to produce a synthetic fuel gas.
*
*
*
*
*
Fluid coking unit means a refinery
process unit in which high molecular
weight petroleum derivatives are
thermally cracked and petroleum coke
is continuously produced in a fluidized
bed system. The fluid coking unit
includes the coking reactor, the coking
burner, and equipment for controlling
air pollutant emissions and for heat
recovery on the fluid coking burner
exhaust vent.
Forced draft process heater means a
process heater in which the combustion
air is supplied under positive pressure
produced by a fan at any location in the
inlet air line prior to the point where the
combustion air enters the process heater
or air preheat. For the purposes of this
subpart, a process heater that uses fans
at both the inlet air side and the exhaust
air side (i.e., balanced draft system) is
considered to be a forced draft process
heater.
Fuel gas means any gas which is
generated at a petroleum refinery and
which is combusted. Fuel gas includes
natural gas when the natural gas is
combined and combusted in any
proportion with a gas generated at a
refinery. Fuel gas does not include gases
generated by catalytic cracking unit
catalyst regenerators, coke calciners
(used to make premium grade coke) and
fluid coking burners, but does include
gases from flexicoking unit gasifiers and
other gasifiers. Fuel gas does not
include vapors that are collected and
combusted in a thermal oxidizer or flare
installed to control emissions from
wastewater treatment units other than
those processing sour water, marine
tank vessel loading operations or
asphalt processing units (i.e., asphalt
blowing stills).
Fuel gas combustion device means
any equipment, such as process heaters
and boilers, used to combust fuel gas.
For the purposes of this subpart, fuel gas
combustion device does not include
flares or facilities in which gases are
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56465
combusted to produce sulfur or sulfuric
acid.
*
*
*
*
*
Natural draft process heater means
any process heater in which the
combustion air is supplied under
ambient or negative pressure without
the use of an inlet air (forced draft) fan.
For the purposes of this subpart, a
natural draft process heater is any
process heater that is not a forced draft
process heater, including induced draft
systems.
Non-emergency flare means any flare
that is not an emergency flare as defined
in this subpart.
*
*
*
*
*
Petroleum refinery means any facility
engaged in producing gasoline,
kerosene, distillate fuel oils, residual
fuel oils, lubricants, asphalt (bitumen)
or other products through distillation of
petroleum or through redistillation,
cracking or reforming of unfinished
petroleum derivatives. A facility that
produces only oil shale or tar sandsderived crude oil for further processing
at a petroleum refinery using only
solvent extraction and/or distillation to
recover diluent is not a petroleum
refinery.
Primary flare means the first flare in
a cascaded flare system.
*
*
*
*
*
Process upset gas means any gas
generated by a petroleum refinery
process unit or by ancillary equipment
as a result of startup, shutdown, upset
or malfunction.
Purge gas means gas introduced
between a flare’s water seal and a flare’s
tip to prevent oxygen infiltration
(backflow) into the flare tip. For flares
with no water seals, the function of
purge gas is performed by sweep gas
(i.e., flares without water seals do not
use purge gas).
*
*
*
*
*
Root cause analysis means an
assessment conducted through a process
of investigation to determine the
primary cause, and any other
contributing cause(s), of a discharge of
gases in excess of specified thresholds.
Secondary flare means a flare in a
cascaded flare system that provides
additional flare capacity and pressure
relief to a flare gas system when the
flare gas flow exceeds the capacity of
the primary flare. For purposes of this
subpart, a secondary flare is
characterized by infrequent use and
must maintain a water seal.
*
*
*
*
*
Sulfur recovery plant means all
process units which recover sulfur from
H2S and/or SO2 from a common source
of sour gas produced at a petroleum
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refinery. The sulfur recovery plant also
includes sulfur pits used to store the
recovered sulfur product, but it does not
include secondary sulfur storage vessels
or loading facilities downstream of the
sulfur pits. For example, a Claus sulfur
recovery plant includes: Reactor furnace
and waste heat boiler, catalytic reactors,
sulfur pits and, if present, oxidation or
reduction control systems or
incinerator, thermal oxidizer or similar
combustion device. Multiple sulfur
recovery units are a single affected
facility only when the units share the
same source of sour gas. Sulfur recovery
plants that receive source gas from
completely segregated sour gas
treatment systems are separate affected
facilities.
Sweep gas means the gas introduced
in a flare gas header system to maintain
a constant flow of gas to prevent oxygen
buildup in the flare header. For flares
with no water seals, sweep gas also
performs the function of preventing
oxygen infiltration (backflow) into the
flare tip.
■ 11. In § 60.102a, lift the stay on
paragraph (g) published December 22,
2008 (73 FR 78552).
■ 12. Section 60.102a is amended by:
■ a. Revising paragraph (a);
■ b. Revising paragraph (f)(1)(ii);
■ c. Revising paragraph (g);
■ d. Removing and reserving paragraph
(h); and
■ e. Revising paragraph (i).
The revisions read as follows:
§ 60.102a
Emissions limitations.
mstockstill on DSK4VPTVN1PROD with RULES3
(a) Each owner or operator that is
subject to the requirements of this
subpart shall comply with the emissions
limitations in paragraphs (b) through (i)
of this section on and after the date on
which the initial performance test,
required by § 60.8, is completed, but not
later than 60 days after achieving the
maximum production rate at which the
affected facility will be operated or 180
days after initial startup, whichever
comes first.
*
*
*
*
*
(f) * * *
(1) * * *
Where:
ERNOx = Daily allowable average emission
rate of NOX, lb/MMBtu (higher heating
value basis);
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(ii) For a sulfur recovery plant with a
reduction control system not followed
by incineration, the owner or operator
shall not discharge or cause the
discharge of any gases into the
atmosphere in excess of 300 ppmv of
reduced sulfur compounds and 10
ppmv of H2S, each calculated as ppmv
SO2 (dry basis) at 0-percent excess air;
or
*
*
*
*
*
(g) Each owner or operator of an
affected fuel gas combustion device
shall comply with the emissions limits
in paragraphs (g)(1) and (2) of this
section.
(1) Except as provided in (g)(1)(iii) of
this section, for each fuel gas
combustion device, the owner or
operator shall comply with either the
emission limit in paragraph (g)(1)(i) of
this section or the fuel gas concentration
limit in paragraph (g)(1)(ii) of this
section.
(i) The owner or operator shall not
discharge or cause the discharge of any
gases into the atmosphere that contain
SO2 in excess of 20 ppmv (dry basis,
corrected to 0-percent excess air)
determined hourly on a 3-hour rolling
average basis and SO2 in excess of 8
ppmv (dry basis, corrected to 0-percent
excess air), determined daily on a 365
successive calendar day rolling average
basis; or
(ii) The owner or operator shall not
burn in any fuel gas combustion device
any fuel gas that contains H2S in excess
of 162 ppmv determined hourly on a 3hour rolling average basis and H2S in
excess of 60 ppmv determined daily on
a 365 successive calendar day rolling
average basis.
(iii) The combustion in a portable
generator of fuel gas released as a result
of tank degassing and/or cleaning is
exempt from the emissions limits in
paragraphs (g)(1)(i) and (ii) of this
section.
(2) For each process heater with a
rated capacity of greater than 40 million
British thermal units per hour (MMBtu/
hr) on a higher heating value basis, the
owner or operator shall not discharge to
the atmosphere any emissions of NOX in
excess of the applicable limits in
paragraphs (g)(2)(i) through (iv) of this
section.
(i) For each natural draft process
heater, comply with the limit in either
paragraph (g)(2)(i)(A) or (B) of this
section. The owner or operator may
comply with either limit at any time,
provided that the appropriate
parameters for each alternative are
monitored as specified in § 60.107a; if
fuel gas composition is not monitored as
specified in § 60.107a(d), the owner or
operator must comply with the
concentration limits in paragraph
(g)(2)(i)(A) of this section.
(A) 40 ppmv (dry basis, corrected to
0-percent excess air) determined daily
on a 30-day rolling average basis; or
(B) 0.040 pounds per million British
thermal units (lb/MMBtu) higher
heating value basis determined daily on
a 30-day rolling average basis.
(ii) For each forced draft process
heater, comply with the limit in either
paragraph (g)(2)(ii)(A) or (B) of this
section. The owner or operator may
comply with either limit at any time,
provided that the appropriate
parameters for each alternative are
monitored as specified in § 60.107a; if
fuel gas composition is not monitored as
specified in § 60.107a(d), the owner or
operator must comply with the
concentration limits in paragraph
(g)(2)(ii)(A) of this section.
(A) 60 ppmv (dry basis, corrected to
0-percent excess air) determined daily
on a 30-day rolling average basis; or
(B) 0.060 lb/MMBtu higher heating
value basis determined daily on a 30day rolling average basis.
(iii) For each co-fired natural draft
process heater, comply with the limit in
either paragraph (g)(2)(iii)(A) or (B) of
this section. The owner or operator must
choose one of the emissions limits with
which to comply at all times:
(A) 150 ppmv (dry basis, corrected to
0-percent excess air) determined daily
on a 30 successive operating day rolling
average basis; or
(B) The daily average emissions limit
calculated using Equation 3 of this
section:
Qgas = Daily average volumetric flow rate of
fuel gas, standard cubic feet per day (scf/
day);
Qoil = Daily average volumetric flow rate of
fuel oil, scf/day;
HHVgas = Daily average higher heating value
of gas fired to the process heater,
MMBtu/scf; and
HHVoil = Daily average higher heating value
of fuel oil fired to the process heater,
MMBtu/scf.
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
56467
(iv) For each co-fired forced draft
process heater, comply with the limit in
either paragraph (g)(2)(iv)(A) or (B) of
this section. The owner or operator must
choose one of the emissions limits with
which to comply at all times:
(A) 150 ppmv (dry basis, corrected to
0-percent excess air) determined daily
on a 30 successive operating day rolling
average basis; or
(B) The daily average emissions limit
calculated using Equation 4 of this
section:
Where:
(i) The design and dimensions of the
process heater, evaluation of available
combustion modification-based
technology, description of fuel gas and,
if applicable, fuel oil characteristics,
information regarding the combustion
conditions (temperature, oxygen
content, firing rates) and other
information needed to demonstrate that
the process heater meets one of the four
classes of process heaters listed in
paragraph (i)(1) of this section.
(ii) An explanation of how the data in
paragraph (i)(2)(i) demonstrate that
ultra-low NOX burners, flue gas
recirculation, control of excess air or
other combustion modification-based
technology (including combinations of
these combustion modification-based
technologies) cannot be used to meet the
applicable emissions limit in paragraph
(g)(2) of this section.
(iii) Results of a performance test
conducted under representative
conditions using the applicable methods
specified in § 60.104a(i) to demonstrate
the performance of the technology the
owner or operator will use to minimize
NOX emissions.
(iv) The means by which the owner or
operator will document continuous
compliance with the site-specific
emissions limit.
(3) The request shall be submitted and
followed as described in paragraphs
(i)(3)(i) through (iii) of this section.
(i) The owner or operator of a process
heater that meets one of the criteria in
paragraphs (i)(1)(i) through (iv) of this
section may request approval from the
Administrator within 180 days after
initial startup of the process heater for
a NOX emissions limit which shall
apply specifically to that affected
facility.
(ii) The request must be submitted to
the Administrator for approval. The
owner or operator must comply with the
request as submitted until it is
approved.
(iii) The request shall also be
submitted to the following address: U.S.
Environmental Protection Agency,
Office of Air Quality Planning and
Standards, Sector Policies and Programs
Division, U.S. EPA Mailroom (E143–01),
Attention: Refinery Sector Lead, 109
T.W. Alexander Drive, Research
Triangle Park, NC 27711. Electronic
copies in lieu of hard copies may also
be submitted to refinerynsps@epa.gov.
(4) The approval process for a request
for a facility-specific NOX emissions
limit is described in paragraphs (i)(4)(i)
through (iii) of this section.
(i) Approval by the Administrator of
a facility-specific NOX emissions limit
request will be based on the
completeness, accuracy and
reasonableness of the request. Factors
that the EPA will consider in reviewing
the request for approval include, but are
not limited to, the following:
(A) A demonstration that the process
heater meets one of the four classes of
process heaters outlined in paragraphs
(i)(1) of this section;
(B) A description of the low-NOX
burner designs and other combustion
modifications considered for reducing
NOX emissions;
(C) The combustion modification
option selected; and
(D) The operating conditions (firing
rate, heater box temperature and excess
oxygen concentration) at which the NOX
emission level was established.
(ii) If the request is approved by the
Administrator, a facility-specific NOX
emissions limit will be established at
the NOX emission level demonstrated in
the approved request.
(iii) If the Administrator finds any
deficiencies in the request, the request
must be revised to address the
deficiencies and be re-submitted for
approval.
■ 13. Section 60.103a is revised to read
as follows:
(h) [Reserved]
(i) For a process heater that meets any
of the criteria of paragraphs (i)(1)(i)
through (iv) of this section, an owner or
operator may request approval from the
Administrator for a NOX emissions limit
which shall apply specifically to that
affected facility. The request shall
include information as described in
paragraph (i)(2) of this section. The
request shall be submitted and followed
as described in paragraph (i)(3) of this
section.
(1) A process heater that meets one of
the criteria in paragraphs (i)(1)(i)
through (iv) of this section may apply
for a site-specific NOX emissions limit:
(i) A modified or reconstructed
process heater that lacks sufficient space
to accommodate installation and proper
operation of combustion modificationbased technology (e.g., ultra-low NOX
burners); or
(ii) A modified or reconstructed
process heater that has downwardly
firing induced draft burners; or
(iii) A co-fired process heater; or
(iv) A process heater operating at
reduced firing conditions for an
extended period of time (i.e., operating
in turndown mode). The site-specific
NOX emissions limit will only apply for
those operating conditions.
(2) The request shall include
sufficient and appropriate data, as
determined by the Administrator, to
allow the Administrator to confirm that
the process heater is unable to comply
with the applicable NOX emissions limit
in paragraph (g)(2) of this section. At a
minimum, the request shall contain the
information described in paragraphs
(i)(2)(i) through (iv) of this section.
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§ 60.103a Design, equipment, work
practice or operational standards.
(a) Except as provided in paragraph
(g) of this section, each owner or
operator that operates a flare that is
subject to this subpart shall develop and
implement a written flare management
plan no later than the date specified in
paragraph (b) of this section. The flare
management plan must include the
information described in paragraphs
(a)(1) through (7) of this section.
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ERNOx = Daily allowable average emission
rate of NOX, lb/MMBtu (higher heating
value basis);
Qgas = Daily average volumetric flow rate of
fuel gas, scf/day;
Qoil = Daily average volumetric flow rate of
fuel oil, scf/day;
HHVgas = Daily average higher heating value
of gas fired to the process heater,
MMBtu/scf; and
HHVoil = Daily average higher heating value
of fuel oil fired to the process heater,
MMBtu/scf.
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
(1) A listing of all refinery process
units, ancillary equipment, and fuel gas
systems connected to the flare for each
affected flare.
(2) An assessment of whether
discharges to affected flares from these
process units, ancillary equipment and
fuel gas systems can be minimized. The
flare minimization assessment must (at
a minimum) consider the items in
paragraphs (a)(2)(i) through (iv) of this
section. The assessment must provide
clear rationale in terms of costs (capital
and annual operating), natural gas offset
credits (if applicable), technical
feasibility, secondary environmental
impacts and safety considerations for
the selected minimization alternative(s)
or a statement, with justifications, that
flow reduction could not be achieved.
Based upon the assessment, each owner
or operator of an affected flare shall
identify the minimization alternatives
that it has implemented by the due date
of the flare management plan and shall
include a schedule for the prompt
implementation of any selected
measures that cannot reasonably be
completed as of that date.
(i) Elimination of process gas
discharge to the flare through process
operating changes or gas recovery at the
source.
(ii) Reduction of the volume of
process gas to the flare through process
operating changes.
(iii) Installation of a flare gas recovery
system or, for facilities that are fuel gas
rich, a flare gas recovery system and a
co-generation unit or combined heat and
power unit.
(iv) Minimization of sweep gas flow
rates and, for flares with water seals,
purge gas flow rates.
(3) A description of each affected flare
containing the information in
paragraphs (a)(3)(i) through (vii) of this
section.
(i) A general description of the flare,
including the information in paragraphs
(a)(3)(i)(A) through (G) of this section.
(A) Whether it is a ground flare or
elevated (including height).
(B) The type of assist system (e.g., air,
steam, pressure, non-assisted).
(C) Whether it is simple or complex
flare tip (e.g., staged, sequential).
(D) Whether the flare is part of a
cascaded flare system (and if so,
whether the flare is primary or
secondary).
(E) Whether the flare serves as a
backup to another flare.
(F) Whether the flare is an emergency
flare or a non-emergency flare.
(G) Whether the flare is equipped
with a flare gas recovery system.
(ii) Description and simple process
flow diagram showing the
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interconnection of the following
components of the flare: flare tip (date
installed, manufacturer, nominal and
effective tip diameter, tip drawing);
knockout or surge drum(s) or pot(s)
(including dimensions and design
capacities); flare header(s) and
subheader(s); assist system; and ignition
system.
(iii) Flare design parameters,
including the maximum vent gas flow
rate; minimum sweep gas flow rate;
minimum purge gas flow rate (if any);
maximum supplemental gas flow rate;
maximum pilot gas flow rate; and, if the
flare is steam-assisted, minimum total
steam rate.
(iv) Description and simple process
flow diagram showing all gas lines
(including flare, purge (if applicable),
sweep, supplemental and pilot gas) that
are associated with the flare. For purge,
sweep, supplemental and pilot gas,
identify the type of gas used. Designate
which lines are exempt from sulfur, H2S
or flow monitoring and why (e.g.,
natural gas, inherently low sulfur, pilot
gas). Designate which lines are
monitored and identify on the process
flow diagram the location and type of
each monitor.
(v) For each flow rate, H2S, sulfur
content, pressure or water seal monitor
identified in paragraph (a)(3)(iv) of this
section, provide a detailed description
of the manufacturer’s specifications,
including, but not limited to, make,
model, type, range, precision, accuracy,
calibration, maintenance and quality
assurance procedures.
(vi) For emergency flares, secondary
flares and flares equipped with a flare
gas recovery system designed, sized and
operated to capture all flows except
those resulting from startup, shutdown
or malfunction:
(A) Description of the water seal,
including the operating range for the
liquid level.
(B) Designation of the monitoring
option elected (flow and sulfur
monitoring or pressure and water seal
liquid level monitoring).
(vii) For flares equipped with a flare
gas recovery system:
(A) A description of the flare gas
recovery system, including number of
compressors and capacity of each
compressor.
(B) A description of the monitoring
parameters used to quantify the amount
of flare gas recovered.
(C) For systems with staged
compressors, the maximum time period
required to begin gas recovery with the
secondary compressor(s), the
monitoring parameters and procedures
used to minimize the duration of
releases during compressor staging and
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a justification for why the maximum
time period cannot be further reduced.
(4) An evaluation of the baseline flow
to the flare. The baseline flow to the
flare must be determined after
implementing the minimization
assessment in paragraph (a)(2) of this
section. Baseline flows do not include
pilot gas flow or purge gas flow (i.e., gas
introduced after the flare’s water seal)
provided these gas flows remain
reasonably constant (i.e., separate flow
monitors for these streams are not
required). Separate baseline flow rates
may be established for different
operating conditions provided that the
management plan includes:
(i) A primary baseline flow rate that
will be used as the default baseline for
all conditions except those specifically
delineated in the plan;
(ii) A description of each special
condition for which an alternate
baseline is established, including the
rationale for each alternate baseline, the
daily flow for each alternate baseline
and the expected duration of the special
conditions for each alternate baseline;
and
(iii) Procedures to minimize
discharges to the affected flare during
each special condition described in
paragraph (a)(4)(ii) of this section,
unless procedures are already
developed for these cases under
paragraph (a)(5) through (7) of this
section, as applicable.
(5) Procedures to minimize or
eliminate discharges to the flare during
the planned startup and shutdown of
the refinery process units and ancillary
equipment that are connected to the
affected flare, together with a schedule
for the prompt implementation of any
procedures that cannot reasonably be
implemented as of the date of the
submission of the flare management
plan.
(6) Procedures to reduce flaring in
cases of fuel gas imbalance (i.e., excess
fuel gas for the refinery’s energy needs),
together with a schedule for the prompt
implementation of any procedures that
cannot reasonably be implemented as of
the date of the submission of the flare
management plan.
(7) For flares equipped with flare gas
recovery systems, procedures to
minimize the frequency and duration of
outages of the flare gas recovery system
and procedures to minimize the volume
of gas flared during such outages,
together with a schedule for the prompt
implementation of any procedures that
cannot reasonably be implemented as of
the date of the submission of the flare
management plan.
(b) Except as provided in paragraph
(g) of this section, each owner or
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operator required to develop and
implement a written flare management
plan as described in paragraph (a) of
this section must submit the plan to the
Administrator as described in
paragraphs (b)(1) through (3) of this
section.
(1) The owner or operator of a newly
constructed or reconstructed flare must
develop and implement the flare
management plan by no later than the
date that the flare becomes an affected
facility subject to this subpart, except
for the selected minimization
alternatives in paragraph (a)(2) and/or
the procedures in paragraphs (a)(5)
though (a)(7) of this section that cannot
reasonably be implemented by that date,
which the owner or operator must
implement in accordance with the
schedule in the flare management plan.
The owner or operator of a modified
flare must develop and implement the
flare management plan by no later than
November 11, 2015 or upon startup of
the modified flare, whichever is later.
(2) The owner or operator must
comply with the plan as submitted by
the date specified in paragraph (b)(1) of
this section. The plan should be
updated periodically to account for
changes in the operation of the flare,
such as new connections to the flare or
the installation of a flare gas recovery
system, but the plan need be resubmitted to the Administrator only if
the owner or operator adds an
alternative baseline flow rate, revises an
existing baseline as described in
paragraph (a)(4) of this section, installs
a flare gas recovery system or is required
to change flare designations and
monitoring methods as described in
§ 60.107a(g). The owner or operator
must comply with the updated plan as
submitted.
(3) All versions of the plan submitted
to the Administrator shall also be
submitted to the following address: U.S.
Environmental Protection Agency,
Office of Air Quality Planning and
Standards, Sector Policies and Programs
Division, U.S. EPA Mailroom (E143–01),
Attention: Refinery Sector Lead, 109
T.W. Alexander Drive, Research
Triangle Park, NC 27711. Electronic
copies in lieu of hard copies may also
be submitted to refinerynsps@epa.gov.
(c) Except as provided in paragraphs
(f) and (g) of this section, each owner or
operator that operates a fuel gas
combustion device, flare or sulfur
recovery plant subject to this subpart
shall conduct a root cause analysis and
a corrective action analysis for each of
the conditions specified in paragraphs
(c)(1) through (3) of this section.
(1) For a flare:
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(i) Any time the SO2 emissions exceed
227 kilograms (kg) (500 lb) in any 24hour period; or
(ii) Any discharge to the flare in
excess of 14,160 standard cubic meters
(m3) (500,000 standard cubic feet (scf))
above the baseline, determined in
paragraph (a)(4) of this section, in any
24-hour period; or
(iii) If the monitoring alternative in
§ 60.107a(g) is elected, any period when
the flare gas line pressure exceeds the
water seal liquid depth, except for
periods attributable to compressor
staging that do not exceed the staging
time specified in paragraph (a)(3)(vii)(C)
of this section.
(2) For a fuel gas combustion device,
each exceedance of an applicable shortterm emissions limit in § 60.102a(g)(1) if
the SO2 discharge to the atmosphere is
227 kg (500 lb) greater than the amount
that would have been emitted if the
emissions limits had been met during
one or more consecutive periods of
excess emissions or any 24-hour period,
whichever is shorter.
(3) For a sulfur recovery plant, each
time the SO2 emissions are more than
227 kg (500 lb) greater than the amount
that would have been emitted if the SO2
or reduced sulfur concentration was
equal to the applicable emissions limit
in § 60.102a(f)(1) or (2) during one or
more consecutive periods of excess
emissions or any 24-hour period,
whichever is shorter.
(d) Except as provided in paragraphs
(f) and (g) of this section, a root cause
analysis and corrective action analysis
must be completed as soon as possible,
but no later than 45 days after a
discharge meeting one of the conditions
specified in paragraphs (c)(1) through
(3) of this section. Special
circumstances affecting the number of
root cause analyses and/or corrective
action analyses are provided in
paragraphs (d)(1) through (5) of this
section.
(1) If a single continuous discharge
meets any of the conditions specified in
paragraphs (c)(1) through (3) of this
section for 2 or more consecutive 24hour periods, a single root cause
analysis and corrective action analysis
may be conducted.
(2) If a single discharge from a flare
triggers a root cause analysis based on
more than one of the conditions
specified in paragraphs (c)(1)(i) through
(iii) of this section, a single root cause
analysis and corrective action analysis
may be conducted.
(3) If the discharge from a flare is the
result of a planned startup or shutdown
of a refinery process unit or ancillary
equipment connected to the affected
flare and the procedures in paragraph
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56469
(a)(5) of this section were followed, a
root cause analysis and corrective action
analysis is not required; however, the
discharge must be recorded as described
in § 60.108a(c)(6) and reported as
described in § 60.108a(d)(5).
(4) If both the primary and secondary
flare in a cascaded flare system meet
any of the conditions specified in
paragraphs (c)(1)(i) through (iii) of this
section in the same 24-hour period, a
single root cause analysis and corrective
action analysis may be conducted.
(5) Except as provided in paragraph
(d)(4) of this section, if discharges occur
that meet any of the conditions
specified in paragraphs (c)(1) through
(3) of this section for more than one
affected facility in the same 24-hour
period, initial root cause analyses shall
be conducted for each affected facility.
If the initial root cause analyses indicate
that the discharges have the same root
cause(s), the initial root cause analyses
can be recorded as a single root cause
analysis and a single corrective action
analysis may be conducted.
(e) Except as provided in paragraphs
(f) and (g) of this section, each owner or
operator of a fuel gas combustion
device, flare or sulfur recovery plant
subject to this subpart shall implement
the corrective action(s) identified in the
corrective action analysis conducted
pursuant to paragraph (d) of this section
in accordance with the applicable
requirements in paragraphs (e)(1)
through (3) of this section.
(1) All corrective action(s) must be
implemented within 45 days of the
discharge for which the root cause and
corrective action analyses were required
or as soon thereafter as practicable. If an
owner or operator concludes that
corrective action should not be
conducted, the owner or operator shall
record and explain the basis for that
conclusion no later than 45 days
following the discharge as specified in
§ 60.108a(c)(6)(ix).
(2) For corrective actions that cannot
be fully implemented within 45 days
following the discharge for which the
root cause and corrective action
analyses were required, the owner or
operator shall develop an
implementation schedule to complete
the corrective action(s) as soon as
practicable.
(3) No later than 45 days following the
discharge for which a root cause and
corrective action analyses were
required, the owner or operator shall
record the corrective action(s)
completed to date, and, for action(s) not
already completed, a schedule for
implementation, including proposed
commencement and completion dates as
specified in § 60.108a(c)(6)(x).
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
(f) Modified flares shall comply with
the requirements of paragraphs (c)
through (e) of this section by November
11, 2015 or at startup of the modified
flare, whichever is later. Modified flares
that were not affected facilities subject
to subpart J of this part prior to
becoming affected facilities under
§ 60.100a shall comply with the
requirements of paragraph (h) of this
section and the requirements of
§ 60.107a(a)(2) by November 11, 2015 or
at startup of the modified flare,
whichever is later. Modified flares that
were affected facilities subject to
subpart J of this part prior to becoming
affected facilities under § 60.100a shall
comply with the requirements of
paragraph (h) of this section and the
requirements of § 60.107a(a)(2) by
November 13, 2012 or at startup of the
modified flare, whichever is later,
except that modified flares that have
accepted applicability of subpart J under
a federal consent decree shall comply
with the subpart J requirements as
specified in the consent decree, but
shall comply with the requirements of
paragraph (h) of this section and the
requirements of § 60.107a(a)(2) by no
later than November 11, 2015.
(g) An affected flare subject to this
subpart located in the Bay Area Air
Quality Management District
(BAAQMD) may elect to comply with
both BAAQMD Regulation 12, Rule 11
and BAAQMD Regulation 12, Rule 12 as
an alternative to complying with the
requirements of paragraphs (a) through
(e) of this section. An affected flare
subject to this subpart located in the
South Coast Air Quality Management
District (SCAQMD) may elect to comply
with SCAQMD Rule 1118 as an
alternative to complying with the
requirements of paragraphs (a) through
(e) of this section. The owner or
operator of an affected flare must notify
the Administrator that the flare is in
compliance with BAAQMD Regulation
12, Rule 11 and BAAQMD Regulation
12, Rule 12 or SCAQMD Rule 1118. The
owner or operator of an affected flare
shall also submit the existing flare
management plan to the following
address: U.S. Environmental Protection
Agency, Office of Air Quality Planning
and Standards, Sector Policies and
Programs Division, U.S. EPA Mailroom
(E143–01), Attention: Refinery Sector
Lead, 109 T.W. Alexander Drive,
Research Triangle Park, NC 27711.
Electronic copies in lieu of hard copies
may also be submitted to
refinerynsps@epa.gov.
(h) Each owner or operator shall not
burn in any affected flare any fuel gas
that contains H2S in excess of 162 ppmv
determined hourly on a 3-hour rolling
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average basis. The combustion in a flare
of process upset gases or fuel gas that is
released to the flare as a result of relief
valve leakage or other emergency
malfunctions is exempt from this limit.
(i) Each owner or operator of a
delayed coking unit shall depressure
each coke drum to 5 lb per square inch
gauge (psig) or less prior to discharging
the coke drum steam exhaust to the
atmosphere. Until the coke drum
pressure reaches 5 psig, the coke drum
steam exhaust must be managed in an
enclosed blowdown system and the
uncondensed vapor must either be
recovered (e.g., sent to the delayed
coking unit fractionators) or vented to
the fuel gas system, a fuel gas
combustion device or a flare.
(j) Alternative means of emission
limitation. (1) Each owner or operator
subject to the provisions of this section
may apply to the Administrator for a
determination of equivalence for any
means of emission limitation that
achieves a reduction in emissions of a
specified pollutant at least equivalent to
the reduction in emissions of that
pollutant achieved by the controls
required in this section.
(2) Determination of equivalence to
the design, equipment, work practice or
operational requirements of this section
will be evaluated by the following
guidelines:
(i) Each owner or operator applying
for a determination of equivalence shall
be responsible for collecting and
verifying test data to demonstrate the
equivalence of the alternative means of
emission limitation.
(ii) For each affected facility for which
a determination of equivalence is
requested, the emission reduction
achieved by the design, equipment,
work practice or operational
requirements shall be demonstrated.
(iii) For each affected facility for
which a determination of equivalence is
requested, the emission reduction
achieved by the alternative means of
emission limitation shall be
demonstrated.
(iv) Each owner or operator applying
for a determination of equivalence to a
work practice standard shall commit in
writing to work practice(s) that provide
for emission reductions equal to or
greater than the emission reductions
achieved by the required work practice.
(v) The Administrator will compare
the demonstrated emission reduction for
the alternative means of emission
limitation to the demonstrated emission
reduction for the design, equipment,
work practice or operational
requirements and, if applicable, will
consider the commitment in paragraph
(j)(2)(iv) of this section.
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(vi) The Administrator may condition
the approval of the alternative means of
emission limitation on requirements
that may be necessary to ensure
operation and maintenance to achieve
the same emissions reduction as the
design, equipment, work practice or
operational requirements.
(3) An owner or operator may offer a
unique approach to demonstrate the
equivalence of any equivalent means of
emission limitation.
(4) Approval of the application for
equivalence to the design, equipment,
work practice or operational
requirements of this section will be
evaluated by the following guidelines:
(i) After a request for determination of
equivalence is received, the
Administrator will publish a notice in
the Federal Register and provide the
opportunity for public hearing if the
Administrator judges that the request
may be approved.
(ii) After notice and opportunity for
public hearing, the Administrator will
determine the equivalence of a means of
emission limitation and will publish the
determination in the Federal Register.
(iii) Any equivalent means of
emission limitations approved under
this section shall constitute a required
work practice, equipment, design or
operational standard within the
meaning of section 111(h)(1) of the
CAA.
(5) Manufacturers of equipment used
to control emissions may apply to the
Administrator for determination of
equivalence for any alternative means of
emission limitation that achieves a
reduction in emissions achieved by the
equipment, design and operational
requirements of this section. The
Administrator will make an equivalence
determination according to the
provisions of paragraphs (j)(2) through
(4) of this section.
■ 14. Section 60.104a is amended by:
■ a. Revising paragraph (a);
■ b. Revising paragraphs (d)(4)(ii),
(d)(4)(iii), (d)(4)(v) and (d)(8);
■ c. Revising paragraph (f)(3);
■ d. Revising paragraph (h)(5)(iv);
■ e. Revising paragraph (i) introductory
text;
■ f. Adding paragraphs (i)(6) through
(i)(8);
■ g. Revising paragraph (j) introductory
text and paragraph (j)(4) introductory
text; and
■ h. Revising paragraph (j)(4)(iv) to read
as follows:
§ 60.104a
Performance tests.
(a) The owner or operator shall
conduct a performance test for each
FCCU, FCU, sulfur recovery plant, flare
and fuel gas combustion device to
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56471
Administrator), but does not apply to
performance tests conducted for the
purpose of obtaining supplemental data
because of continuous monitoring
system breakdowns, repairs, calibration
checks and zero and span adjustments.
*
*
*
*
*
(d) * * *
(4) * * *
(ii) The emissions rate of PM (EPM) is
computed for each run using Equation
5 of this section:
Where:
E = Emission rate of PM, g/kg (lb/1,000 lb)
of coke burn-off;
cs = Concentration of total PM, grams per dry
standard cubic meter (g/dscm) (gr/dscf);
Qsd = Volumetric flow rate of effluent gas, dry
standard cubic meters per hour (dry
standard cubic feet per hour);
Rc = Coke burn-off rate, kilograms per hour
(kg/hr) [lb per hour (lb/hr)] coke; and
K = Conversion factor, 1.0 grams per gram
(7,000 grains per lb).
Where:
Rc = Coke burn-off rate, kg/hr (lb/hr);
Qr = Volumetric flow rate of exhaust gas from
FCCU regenerator or fluid coking burner
before any emissions control or energy
recovery system that burns auxiliary
fuel, dry standard cubic meters per
minute (dscm/min) [dry standard cubic
feet per minute (dscf/min)];
Qa = Volumetric flow rate of air to FCCU
regenerator or fluid coking burner, as
determined from the unit’s control room
instrumentation, dscm/min (dscf/min);
Qoxy = Volumetric flow rate of O2 enriched
air to FCCU regenerator or fluid coking
unit, as determined from the unit’s
control room instrumentation, dscm/min
(dscf/min);
%CO2 = Carbon dioxide (CO2) concentration
in FCCU regenerator or fluid coking
burner exhaust, percent by volume (dry
basis);
%CO = CO concentration in FCCU
regenerator or fluid coking burner
exhaust, percent by volume (dry basis);
%O2 = O2 concentration in FCCU regenerator
or fluid coking burner exhaust, percent
by volume (dry basis);
%Ooxy = O2 concentration in O2 enriched air
stream inlet to the FCCU regenerator or
fluid coking burner, percent by volume
(dry basis);
K1 = Material balance and conversion factor,
0.2982 (kg-min)/(hr-dscm-%) [0.0186 (lbmin)/(hr-dscf-%)];
Where:
Qr = Volumetric flow rate of exhaust gas from
FCCU regenerator or fluid coking burner
before any emission control or energy
recovery system that burns auxiliary
fuel, dscm/min (dscf/min);
Qa = Volumetric flow rate of air to FCCU
regenerator or fluid coking burner, as
determined from the unit’s control room
instrumentation, dscm/min (dscf/min);
Qoxy = Volumetric flow rate of O2 enriched
air to FCCU regenerator or fluid coking
unit, as determined from the unit’s
control room instrumentation, dscm/min
(dscf/min);
%CO2 = Carbon dioxide concentration in
FCCU regenerator or fluid coking burner
exhaust, percent by volume (dry basis);
%CO = CO concentration FCCU regenerator
or fluid coking burner exhaust, percent
by volume (dry basis). When no auxiliary
fuel is burned and a continuous CO
monitor is not required in accordance
with § 60.105a(h)(3), assume %CO to be
zero;
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(iii) The coke burn-off rate (Rc) is
computed for each run using Equation
6 of this section:
K2 = Material balance and conversion factor,
2.088 (kg-min)/(hr-dscm) [0.1303 (lbmin)/(hr-dscf)]; and
K3 = Material balance and conversion factor,
0.0994 (kg-min)/(hr-dscm-%) [0.00624
(lb-min)/(hr-dscf-%)].
*
*
*
*
(v) For subsequent calculations of
coke burn-off rates or exhaust gas flow
rates, the volumetric flow rate of Qr is
calculated using average exhaust gas
concentrations as measured by the
monitors required in § 60.105a(b)(2), if
applicable, using Equation 7 of this
section:
*
*
*
*
*
(8) The owner or operator shall adjust
PM, NOX, SO2 and CO pollutant
concentrations to 0-percent excess air or
0-percent O2 using Equation 8 of this
section:
E:\FR\FM\12SER3.SGM
12SER3
ER12SE12.004
%O2 = O2 concentration in FCCU regenerator
or fluid coking burner exhaust, percent
by volume (dry basis); and
%Ooxy = O2 concentration in O2 enriched air
stream inlet to the FCCU regenerator or
fluid coking burner, percent by volume
(dry basis).
ER12SE12.005
*
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demonstrate initial compliance with
each applicable emissions limit in
§ 60.102a according to the requirements
of § 60.8. The notification requirements
of § 60.8(d) apply to the initial
performance test and to subsequent
performance tests required by paragraph
(b) of this section (or as required by the
Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
Where:
Cadj = pollutant concentration adjusted to 0percent excess air or O2, parts per
million (ppm) or g/dscm;
Cmeas = pollutant concentration measured on
a dry basis, ppm or g/dscm;
20.9c = 20.9 percent O2¥0.0 percent O2
(defined O2 correction basis), percent;
20.9 = O2 concentration in air, percent; and
%O2 = O2 concentration measured on a dry
basis, percent.
Where:
Opacity limit = Maximum permissible 3-hour
average opacity, percent, or 10 percent,
whichever is greater;
Opacityst = Hourly average opacity measured
during the source test, percent; and
PMEmRst = PM emission rate measured
during the source test, lb/1,000 lb coke
burn.
of the NOX concentrations from each of
the three test runs. If the NOX
concentration for the performance test is
less than or equal to the numerical value
of the applicable NOX emissions limit
(regardless of averaging time), then the
test is considered to be a valid test.
(C) Determine the average O2
concentration for each test run of a valid
test.
(D) Calculate the O2 operating limit as
the average O2 concentration of the
three test runs from a valid test.
(ii) If an O2 operating curve will be
used:
(A) Conduct a performance test
following the methods provided in
paragraphs (i)(1), (2), (3) and (5) of this
section at a representative condition for
each operating range for which different
O2 operating limits will be established.
Different operating conditions may be
defined as different firing rates (e.g.,
above 50 percent of rated heat capacity
and at or below 50 percent of rated heat
capacity) and/or, for co-fired process
heaters, different fuel mixtures (e.g.,
primarily gas fired, primarily oil fired,
and equally co-fired, i.e., approximately
50 percent of the input heating value is
from fuel gas and approximately 50
percent of the input heating value is
from fuel oil). Performance tests for
different operating ranges may be
conducted at different times.
(B) Each test will consist of three test
runs. Calculate the NOX concentration
for the performance test as the average
of the NOX concentrations from each of
the three test runs. If the NOX
concentration for the performance test is
less than or equal to the numerical value
of the applicable NOX emissions limit
(regardless of averaging time), then the
test is considered to be a valid test.
(C) If an operating curve is developed
for different firing rates, conduct at least
one test when the process heater is
firing at no less than 70 percent of the
rated heat capacity and at least one test
under turndown conditions (i.e., when
the process heater is firing at 50 percent
*
*
*
*
(h) * * *
(5) * * *
(iv) The owner or operator shall use
Equation 8 of this section to adjust
pollutant concentrations to 0-percent O2
or 0- percent excess air.
(i) The owner or operator shall
determine compliance with the SO2 and
NOX emissions limits in § 60.102a(g) for
a fuel gas combustion device according
to the following test methods and
procedures:
*
*
*
*
*
(6) For process heaters with a rated
heat capacity between 40 and 100
MMBtu/hr that elect to demonstrate
continuous compliance with a
maximum excess oxygen limit as
provided in § 60.107a(c)(6) or (d)(8), the
owner or operator shall establish the O2
operating limit or O2 operating curve
based on the performance test results
according to the requirements in
paragraph (i)(6)(i) or (ii) of this section,
respectively.
(i) If a single O2 operating limit will
be used:
(A) Conduct the performance test
following the methods provided in
paragraphs (i)(1), (2), (3) and (5) of this
section when the process heater is firing
at no less than 70 percent of the rated
heat capacity. For co-fired process
heaters, conduct at least one of the test
runs while the process heater is being
supplied by both fuel gas and fuel oil
and conduct at least one of the test runs
while the process heater is being
supplied solely by fuel gas.
(B) Each test will consist of three test
runs. Calculate the NOX concentration
for the performance test as the average
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*
*
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*
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*
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or less of the rated heat capacity). If O2
operating limits are developed for cofired process heaters based only on
overall firing rates (and not by fuel
mixtures), conduct at least one of the
test runs for each test while the process
heater is being supplied by both fuel gas
and fuel oil and conduct at least one of
the test runs while the process heater is
being supplied solely by fuel gas.
(D) Determine the average O2
concentration for each test run of a valid
test.
(E) Calculate the O2 operating limit for
each operating range as the average O2
concentration of the three test runs from
a valid test conducted at the
representative conditions for that given
operating range.
(F) Identify the firing rates for which
the different operating limits apply. If
only two operating limits are
established based on firing rates, the O2
operating limits established when the
process heater is firing at no less than
70 percent of the rated heat capacity
must apply when the process heater is
firing above 50 percent of the rated heat
capacity and the O2 operating limits
established for turndown conditions
must apply when the process heater is
firing at 50 percent or less of the rated
heat capacity.
(G) Operating limits associated with
each interval will be valid for 2 years or
until another operating limit is
established for that interval based on a
more recent performance test specific
for that interval, whichever occurs first.
Owners and operators must use the
operating limits determined for a given
interval based on the most recent
performance test conducted for that
interval.
(7) The owner or operator of a process
heater complying with a NOX limit in
terms of lb/MMBtu as provided in
§ 60.102a(g)(2)(i)(B), (g)(2)(ii)(B),
(g)(2)(iii)(B) or (g)(2)(iv)(B) or a process
heater with a rated heat capacity
between 40 and 100 MMBtu/hr that
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*
*
(f) * * *
(3) Compute the site-specific limit
using Equation 9 of this section:
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elects to demonstrate continuous
compliance with a maximum excess O2
limit, as provided in § 60.107a(c)(6) or
(d)(8), shall determine heat input to the
process heater in MMBtu/hr during each
performance test run by measuring fuel
gas flow rate, fuel oil flow rate (as
applicable) and heating value content
according to the methods provided in
§ 60.107a(d)(5), (d)(6), and (d)(4) or
(d)(7), respectively.
(8) The owner or operator shall use
Equation 8 of this section to adjust
pollutant concentrations to 0-percent O2
or 0- percent excess air.
(j) The owner or operator shall
determine compliance with the
applicable H2S emissions limit in
§ 60.102a(g)(1) for a fuel gas combustion
device or the concentration requirement
in § 60.103a(h) for a flare according to
the following test methods and
procedures:
*
*
*
*
*
(4) EPA Method 11, 15 or 15A of
Appendix A–5 to part 60 or EPA
Method 16 of Appendix A–6 to part 60
for determining the H2S concentration
for affected facilities using an H2S
monitor as specified in § 60.107a(a)(2).
The method ANSI/ASME PTC 19.10–
1981 (incorporated by reference—see
§ 60.17) is an acceptable alternative to
EPA Method 15A of Appendix A–5 to
part 60. The owner or operator may
demonstrate compliance based on the
mixture used in the fuel gas combustion
device or flare or for each individual
fuel gas stream used in the fuel gas
combustion device or flare.
*
*
*
*
*
(iv) If monitoring is conducted at a
single point in a common source of fuel
gas as allowed under § 60.107a(a)(2)(iv),
only one performance test is required.
That is, performance tests are not
required when a new affected fuel gas
combustion device or flare is added to
a common source of fuel gas that
previously demonstrated compliance.
■ 15. Section 60.105a is amended by:
■ a. Revising paragraph (b) introductory
text, and paragraph (b)(1) introductory
text, and paragraphs (b)(1)(ii)(A),
(b)(2)(i) and (b)(2)(ii); and
■ b. Revising paragraph (i)(5) to read as
follows:
§ 60.105a Monitoring of emissions and
operations for fluid catalytic cracking units
(FCCU) and fluid coking units (FCU).
*
*
*
*
*
(b) Control device operating
parameters. Each owner or operator of
a FCCU or FCU subject to the PM per
coke burn-off emissions limit in
§ 60.102a(b)(1) that uses a control device
other than fabric filter or cyclone shall
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comply with the requirements in
paragraphs (b)(1) and (2) of this section.
(1) The owner or operator shall
install, operate and maintain continuous
parameter monitor systems (CPMS) to
measure and record operating
parameters for each control device
according to the applicable
requirements in paragraphs (b)(1)(i)
through (v) of this section.
*
*
*
*
*
(ii) * * *
(A) As an alternative to pressure drop,
the owner or operator of a jet ejector
type wet scrubber or other type of wet
scrubber equipped with atomizing spray
nozzles must conduct a daily check of
the air or water pressure to the spray
nozzles and record the results of each
check.
*
*
*
*
*
(2) * * *
(i) The owner or operator shall install,
operate and maintain each monitor
according to Performance Specifications
3 and 4 of Appendix B to part 60.
(ii) The owner or operator shall
conduct performance evaluations of
each CO2, O2 and CO monitor according
to the requirements in § 60.13(c) and
Performance Specifications 3 and 4 of
Appendix B to part 60. The owner or
operator shall use EPA Method 3 of
Appendix A–3 to part 60 and EPA
Method 10, 10A or 10B of Appendix A–
4 to part 60 for conducting the relative
accuracy evaluations.
*
*
*
*
*
(i) * * *
(5) All rolling 7-day periods during
which the average concentration of SO2
as measured by the SO2 CEMS under
§ 60.105a(g) exceeds 50 ppmv, and all
rolling 365-day periods during which
the average concentration of SO2 as
measured by the SO2 CEMS exceeds 25
ppmv.
*
*
*
*
*
■ 16. In § 60.107a, lift the stay on
paragraphs (d) and (e) published
December 22, 2008 (73 FR 78552).
■ 17. Section 60.107a is amended by:
■ a. Revising the section heading;
■ b. Revising paragraph (a) introductory
text, paragraph (a)(1) introductory text,
paragraph (a)(2) introductory text,
(a)(2)(i), (a)(2)(iv) and paragraph (a)(3)
introductory text;
■ c. Adding paragraphs (a)(2)(v) and
(a)(2)(vi);
■ d. Revising paragraph (b) introductory
text and paragraphs (b)(1)(i), (b)(1)(v)
and (b)(3)(iii);
■ e. Revising paragraph (c) introductory
text and paragraphs (c)(1) and (c)(6);
■ f. Redesignating paragraphs (d), (e),
and (f) as paragraphs (e), (f) and (i),
respectively;
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56473
g. Adding a new paragraph (d);
h. Revising newly redesignated
paragraph (e);
■ i. Revising newly redesignated
paragraph (f);
■ j. Adding a new paragraph (g);
■ k. Adding a new paragraph (h); and
■ l. Revising newly redesignated
paragraph (i).
The revisions and additions read as
follows:
■
■
§ 60.107a Monitoring of emissions and
operations for fuel gas combustion devices
and flares.
(a) Fuel gas combustion devices
subject to SO2 or H2S limit and flares
subject to H2S concentration
requirements. The owner or operator of
a fuel gas combustion device that is
subject to § 60.102a(g)(1) and elects to
comply with the SO2 emission limits in
§ 60.102a(g)(1)(i) shall comply with the
requirements in paragraph (a)(1) of this
section. The owner or operator of a fuel
gas combustion device that is subject to
§ 60.102a(g)(1) and elects to comply
with the H2S concentration limits in
§ 60.102a(g)(1)(ii) or a flare that is
subject to the H2S concentration
requirement in § 60.103a(h) shall
comply with paragraph (a)(2) of this
section.
(1) The owner or operator of a fuel gas
combustion device that elects to comply
with the SO2 emissions limits in
§ 60.102a(g)(1)(i) shall install, operate,
calibrate and maintain an instrument for
continuously monitoring and recording
the concentration (dry basis, 0-percent
excess air) of SO2 emissions into the
atmosphere. The monitor must include
an O2 monitor for correcting the data for
excess air.
*
*
*
*
*
(2) The owner or operator of a fuel gas
combustion device that elects to comply
with the H2S concentration limits in
§ 60.102a(g)(1)(ii) or a flare that is
subject to the H2S concentration
requirement in § 60.103a(h) shall install,
operate, calibrate and maintain an
instrument for continuously monitoring
and recording the concentration by
volume (dry basis) of H2S in the fuel
gases before being burned in any fuel
gas combustion device or flare.
(i) The owner or operator shall install,
operate and maintain each H2S monitor
according to Performance Specification
7 of Appendix B to part 60. The span
value for this instrument is 300 ppmv
H2S.
*
*
*
*
*
(iv) Fuel gas combustion devices or
flares having a common source of fuel
gas may be monitored at only one
location, if monitoring at this location
accurately represents the concentration
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of H2S in the fuel gas being burned in
the respective fuel gas combustion
devices or flares.
(v) The owner or operator of a flare
subject to § 60.103a(c) through (e) may
use the instrument required in
paragraph (e)(1) of this section to
demonstrate compliance with the H2S
concentration requirement in
§ 60.103a(h) if the owner or operator
complies with the requirements of
paragraph (e)(1)(i) through (iv) and if the
instrument has a span (or dual span, if
necessary) capable of accurately
measuring concentrations between 20
and 300 ppmv. If the instrument
required in paragraph (e)(1) of this
section is used to demonstrate
compliance with the H2S concentration
requirement, the concentration directly
measured by the instrument must meet
the numeric concentration in
§ 60.103a(h).
(vi) The owner or operator of
modified flare that meets all three
criteria in paragraphs (a)(2)(vi)(A)
through (C) of this section shall comply
with the requirements of paragraphs
(a)(2)(i) through (v) of this section no
later than November 11, 2015. The
owner or operator shall comply with the
approved alternative monitoring plan or
plans pursuant to § 60.13(i) until the
flare is in compliance with requirements
of paragraphs (a)(2)(i) through (v) of this
section.
(A) The flare was an affected facility
subject to subpart J of this part prior to
becoming an affected facility under
§ 60.100a.
(B) The owner or operator had an
approved alternative monitoring plan or
plans pursuant to § 60.13(i) for all fuel
gases combusted in the flare.
(C) The flare did not have in place on
or before September 12, 2012 an
instrument for continuously monitoring
and recording the concentration by
volume (dry basis) of H2S in the fuel
gases that is capable of complying with
the requirements of paragraphs (a)(2)(i)
through (v) of this section.
(3) The owner or operator of a fuel gas
combustion device or flare is not
required to comply with paragraph
(a)(1) or (2) of this section for fuel gas
streams that are exempt under
§§ 60.102a(g)(1)(iii) or 60.103a(h) or, for
fuel gas streams combusted in a process
heater, other fuel gas combustion device
or flare that are inherently low in sulfur
content. Fuel gas streams meeting one of
the requirements in paragraphs (a)(3)(i)
through (iv) of this section will be
considered inherently low in sulfur
content.
*
*
*
*
*
(b) Exemption from H2S monitoring
requirements for low-sulfur fuel gas
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streams. The owner or operator of a fuel
gas combustion device or flare may
apply for an exemption from the H2S
monitoring requirements in paragraph
(a)(2) of this section for a fuel gas stream
that is inherently low in sulfur content.
A fuel gas stream that is demonstrated
to be low-sulfur is exempt from the
monitoring requirements of paragraphs
(a)(1) and (2) of this section until there
are changes in operating conditions or
stream composition.
(1) * * *
(i) A description of the fuel gas
stream/system to be considered,
including submission of a portion of the
appropriate piping diagrams indicating
the boundaries of the fuel gas stream/
system and the affected fuel gas
combustion device(s) or flare(s) to be
considered;
*
*
*
*
*
(v) A description of how the 2 weeks
(or seven samples for infrequently
operated fuel gas streams/systems) of
monitoring results compares to the
typical range of H2S concentration (fuel
quality) expected for the fuel gas
stream/system going to the affected fuel
gas combustion device or flare (e.g., the
2 weeks of daily detector tube results for
a frequently operated loading rack
included the entire range of products
loaded out and, therefore, should be
representative of typical operating
conditions affecting H2S content in the
fuel gas stream going to the loading rack
flare).
*
*
*
*
*
(3) * * *
(iii) If the operation change results in
a sulfur content that is outside the range
of concentrations included in the
original application and the owner or
operator chooses not to submit new
information to support an exemption,
the owner or operator must begin H2S
monitoring using daily stain sampling to
demonstrate compliance. The owner or
operator must begin monitoring
according to the requirements in
paragraphs (a)(1) or (a)(2) of this section
as soon as practicable, but in no case
later than 180 days after the operation
change. During daily stain tube
sampling, a daily sample exceeding 162
ppmv is an exceedance of the 3-hour
H2S concentration limit. The owner or
operator of a fuel gas combustion device
must also determine a rolling 365-day
average using the stain sampling results;
an average H2S concentration of 5 ppmv
must be used for days within the rolling
365-day period prior to the operation
change.
(c) Process heaters complying with the
NOX concentration-based limit. The
owner or operator of a process heater
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subject to the NOX emissions limit in
§ 60.102a(g)(2) and electing to comply
with the applicable emissions limit in
§ 60.102a(g)(2)(i)(A), (g)(2)(ii)(A),
(g)(2)(iii)(A) or (g)(2)(iv)(A) shall install,
operate, calibrate and maintain an
instrument for continuously monitoring
and recording the concentration (dry
basis, 0-percent excess air) of NOX
emissions into the atmosphere
according to the requirements in
paragraphs (c)(1) through (5) of this
section, except as provided in paragraph
(c)(6) of this section. The monitor must
include an O2 monitor for correcting the
data for excess air.
(1) Except as provided in paragraph
(c)(6) of this section, the owner or
operator shall install, operate and
maintain each NOX monitor according
to Performance Specification 2 of
Appendix B to part 60. The span value
of this NOX monitor must be between 2
and 3 times the applicable emissions
limit, inclusive.
*
*
*
*
*
(6) The owner or operator of a process
heater that has a rated heating capacity
of less than 100 MMBtu and is equipped
with combustion modification-based
technology to reduce NOX emissions
(i.e., low-NOX burners, ultra-low-NOX
burners) may elect to comply with the
monitoring requirements in paragraphs
(c)(1) through (5) of this section or,
alternatively, the owner or operator of
such a process heater shall conduct
biennial performance tests according to
the requirements in § 60.104a(i),
establish a maximum excess O2
operating limit or operating curve
according to the requirements in
§ 60.104a(i)(6) and comply with the O2
monitoring requirements in paragraphs
(c)(3) through (5) of this section to
demonstrate compliance. If an O2
operating curve is used (i.e., if different
O2 operating limits are established for
different operating ranges), the owner or
operator of the process heater must also
monitor fuel gas flow rate, fuel oil flow
rate (as applicable) and heating value
content according to the methods
provided in paragraphs (d)(5), (d)(6),
and (d)(4) or (d)(7) of this section,
respectively.
(d) Process heaters complying with
the NOX heating value-based or massbased limit. The owner or operator of a
process heater subject to the NOX
emissions limit in § 60.102a(g)(2) and
electing to comply with the applicable
emissions limit in § 60.102a(g)(2)(i)(B)
or (g)(2)(ii)(B) shall install, operate,
calibrate and maintain an instrument for
continuously monitoring and recording
the concentration (dry basis, 0-percent
excess air) of NOX emissions into the
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56475
section 12.3.2 of EPA Method 19 of
Appendix A–7 to part 60 to determine
the F factor on a dry basis. If a single
fuel gas system provides fuel gas to
several process heaters, the F factor may
be determined at a single location in the
fuel gas system provided it is
representative of the fuel gas fed to the
affected process heater(s).
(3) As an alternative to the
requirements in paragraph (d)(2) of this
section, the owner or operator of a gasfired process heater shall install, operate
and maintain a gas composition
analyzer and determine the average F
factor of the fuel gas using the factors in
Table 1 of this subpart and Equation 10
of this section. If a single fuel gas system
provides fuel gas to several process
heaters, the F factor may be determined
at a single location in the fuel gas
system provided it is representative of
the fuel gas fed to the affected process
heater(s).
volumetric flow meters, temperature
and pressure monitors must be installed
in conjunction with the flow meter or in
a representative location to correct the
measured flow to standard conditions
(i.e., 68 °F and 1 atmosphere). For mass
flow meters, use gas compositions
determined according to paragraph
(d)(4) of this section to determine the
average molecular weight of the fuel gas
and convert the mass flow to a
volumetric flow at standard conditions
(i.e., 68 °F and 1 atmosphere). The
owner or operator shall conduct
performance evaluations of each fuel gas
flow monitor according to the
requirements in § 60.13 and
Performance Specification 6 of
Appendix B to part 60. Any of the
following methods shall be used for
conducting the relative accuracy
evaluations:
(i) EPA Method 2, 2A, 2B, 2C or 2D
of Appendix A–2 to part 60;
(ii) ASME MFC–3M–2004
(incorporated by reference-see § 60.17);
(iii) ANSI/ASME MFC–4M–1986
(Reaffirmed 2008) (incorporated by
reference-see § 60.17);
(iv) ASME MFC–6M–1998
(Reaffirmed 2005) (incorporated by
reference-see § 60.17);
(v) ASME/ANSI MFC–7M–1987
(Reaffirmed 2006) (incorporated by
reference-see § 60.17);
(vi) ASME MFC–11M–2006
(incorporated by reference-see § 60.17);
(vii) ASME MFC–14M–2003
(incorporated by reference-see § 60.17);
(viii) ASME MFC–18M–2001
(incorporated by reference-see § 60.17);
(ix) AGA Report No. 3, Part 1
(incorporated by reference-see § 60.17);
(x) AGA Report No. 3, Part 2
(incorporated by reference-see § 60.17);
(xi) AGA Report No. 11 (incorporated
by reference-see § 60.17);
(xii) AGA Report No. 7 (incorporated
by reference-see § 60.17); and
(xiii) API Manual of Petroleum
Measurement Standards, Chapter 22,
Section 2 (incorporated by reference-see
§ 60.17).
(6) The owner or operator shall
install, operate and maintain each fuel
oil flow monitor according to the
manufacturer’s recommendations. The
owner or operator shall conduct
performance evaluations of each fuel oil
flow monitor according to the
requirements in § 60.13 and
Performance Specification 6 of
Appendix B to part 60. Any of the
following methods shall be used for
conducting the relative accuracy
evaluations:
(i) Any one of the methods listed in
paragraph (d)(5) of this section that are
applicable to fuel oil (i.e., ‘‘fluids’’);
(ii) ANSI/ASME–MFC–5M–1985
(Reaffirmed 2006) (incorporated by
reference-see § 60.17);
(4) The owner or operator shall
conduct performance evaluations of
each compositional monitor according
to the requirements in Performance
Specification 9 of Appendix B to part
60. Any of the following methods shall
be used for conducting the relative
accuracy evaluations:
(i) EPA Method 18 of Appendix A–6
to part 60;
(ii) ASTM D1945–03 (Reapproved
2010)(incorporated by reference-see
§ 60.17);
(iii) ASTM D1946–90 (Reapproved
2006)(incorporated by reference-see
§ 60.17);
(iv) ASTM D6420–99 (Reapproved
2004)(incorporated by reference-see
§ 60.17);
(v) GPA 2261–00 (incorporated by
reference-see § 60.17); or
(vi) ASTM UOP539–97 (incorporated
by reference-see § 60.17).
(5) The owner or operator shall
install, operate and maintain fuel gas
flow monitors according to the
manufacturer’s recommendations. For
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er12se12.008
paragraph (d)(5) and (6) of this section;
for fuel gas streams, determine gas
composition according to the
requirements in paragraph (d)(4) of this
section or the higher heating value
according to the requirements in
paragraph (d)(7) of this section; and for
fuel oil streams, determine the heating
value according to the monitoring
requirements in paragraph (d)(7) of this
section.
(1) Except as provided in paragraph
(d)(8) of this section, the owner or
operator shall install, operate and
maintain each NOX monitor according
to the requirements in paragraphs (c)(1)
through (5) of this section. The monitor
must include an O2 monitor for
correcting the data for excess air.
(2) Except as provided in paragraph
(d)(3) of this section, the owner or
operator shall sample and analyze each
fuel stream fed to the process heater
using the methods and equations in
Where:
Fd = F factor on dry basis at 0-percent excess
air, dscf/MMBtu.
Xi = mole or volume fraction of each
component in the fuel gas.
MEVi = molar exhaust volume, dry standard
cubic feet per mole (dscf/mol).
MHCi = molar heat content, Btu per mole
(Btu/mol).
1,000,000 = unit conversion, Btu per MMBtu.
mstockstill on DSK4VPTVN1PROD with RULES3
atmosphere and shall determine the F
factor of the fuel gas stream no less
frequently than once per day according
to the monitoring requirements in
paragraphs (d)(1) through (4) of this
section. The owner or operator of a cofired process heater subject to the NOX
emissions limit in § 60.102a(g)(2) and
electing to comply with the heating
value-based limit in
§ 60.102a(g)(2)(iii)(B) or (g)(2)(iv)(B)
shall install, operate, calibrate and
maintain an instrument for
continuously monitoring and recording
the concentration (dry basis, 0-percent
excess air) of NOX emissions into the
atmosphere according to the monitoring
requirements in paragraph (d)(1) of this
section; install, operate, calibrate and
maintain an instrument for
continuously monitoring and recording
the flow rate of the fuel gas and fuel oil
fed to the process heater according to
the monitoring requirements in
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(iii) ASME/ANSI MFC–9M–1988
(Reaffirmed 2006) (incorporated by
reference-see § 60.17);
(iv) ASME MFC–16–2007
(incorporated by reference-see § 60.17);
(v) ASME MFC–22–2007
(incorporated by reference-see § 60.17);
or
(vi) ISO 8316 (incorporated by
reference-see § 60.17).
(7) The owner or operator shall
determine the higher heating value of
each fuel fed to the process heater using
any of the applicable methods included
in paragraphs (d)(7)(i) through (ix) of
this section. If a common fuel supply
system provides fuel gas or fuel oil to
several process heaters, the higher
heating value of the fuel in each fuel
supply system may be determined at a
single location in the fuel supply system
provided it is representative of the fuel
fed to the affected process heater(s). The
higher heating value of each fuel fed to
the process heater must be determined
no less frequently than once per day
except as provided in paragraph
(d)(7)(x) of this section.
(i) ASTM D240–02 (Reapproved 2007)
(incorporated by reference-see § 60.17).
(ii) ASTM D1826–94 (Reapproved
2003) (incorporated by reference-see
§ 60.17).
(iii) ASTM D1945–03 (Reapproved
2010) (incorporated by reference-see
§ 60.17).
(iv) ASTM D1946–90 (Reapproved
2006) (incorporated by reference-see
§ 60.17).
(v) ASTM D3588–98 (Reapproved
2003) (incorporated by reference-see
§ 60.17).
(vi) ASTM D4809–06 (incorporated by
reference-see § 60.17).
(vii) ASTM D4891–89 (Reapproved
2006) (incorporated by reference-see
§ 60.17).
(viii) GPA 2172–09 (incorporated by
reference-see § 60.17).
(ix) Any of the methods specified in
section 2.2.7 of Appendix D to part 75.
(x) If the fuel oil supplied to the
affected co-fired process heater
originates from a single storage tank, the
owner or operator may elect to use the
storage tank sampling method in section
2.2.4.2 of Appendix D to part 75 instead
of daily sampling, except that the most
recent value for heating content must be
used.
(8) The owner or operator of a process
heater that has a rated heating capacity
of less than 100 MMBtu and is equipped
with combustion modification based
technology to reduce NOX emissions
(i.e., low-NOX burners or ultra-low NOX
burners) may elect to comply with the
monitoring requirements in paragraphs
(d)(1) through (7) of this section or,
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alternatively, the owner or operator of
such a process heater shall conduct
biennial performance tests according to
the requirements in § 60.104a(i),
establish a maximum excess O2
operating limit or operating curve
according to the requirements in
§ 60.104a(i)(6) and comply with the O2
monitoring requirements in paragraphs
(c)(3) through (5) of this section to
demonstrate compliance. If an O2
operating curve is used (i.e., if different
O2 operating limits are established for
different operating ranges), the owner or
operator of the process heater must also
monitor fuel gas flow rate, fuel oil flow
rate (as applicable) and heating value
content according to the methods
provided in paragraphs (d)(5), (d)(6),
and (d)(4) or (d)(7) of this section,
respectively.
(e) Sulfur monitoring for assessing
root cause analysis threshold for
affected flares. Except as described in
paragraphs (e)(4) and (h) of this section,
the owner or operator of an affected
flare subject to § 60.103a(c) through (e)
shall determine the total reduced sulfur
concentration for each gas line directed
to the affected flare in accordance with
either paragraph (e)(1), (e)(2) or (e)(3) of
this section. Different options may be
elected for different gas lines. If a
monitoring system is in place that is
capable of complying with the
requirements related to either paragraph
(e)(1), (e)(2) or (e)(3) of this section, the
owner or operator of a modified flare
must comply with the requirements
related to either paragraph (e)(1), (e)(2)
or (e)(3) of this section upon startup of
the modified flare. If a monitoring
system is not in place that is capable of
complying with the requirements
related to either paragraph (e)(1), (e)(2)
or (e)(3) of this section, the owner or
operator of a modified flare must
comply with the requirements related to
either paragraph (e)(1), (e)(2) or (e)(3) of
this section no later than November 11,
2015 or upon startup of the modified
flare, whichever is later.
(1) Total reduced sulfur monitoring
requirements. The owner or operator
shall install, operate, calibrate and
maintain an instrument for
continuously monitoring and recording
the concentration of total reduced sulfur
in gas discharged to the flare.
(i) The owner or operator shall install,
operate and maintain each total reduced
sulfur monitor according to Performance
Specification 5 of Appendix B to part
60. The span value should be
determined based on the maximum
sulfur content of gas that can be
discharged to the flare (e.g., roughly 1.1
to 1.3 times the maximum anticipated
sulfur concentration), but may be no
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less than 5,000 ppmv. A single dual
range monitor may be used to comply
with the requirements of this paragraph
and paragraph (a)(2) of this section
provided the applicable span
specifications are met.
(ii) The owner or operator shall
conduct performance evaluations of
each total reduced sulfur monitor
according to the requirements in
§ 60.13(c) and Performance
Specification 5 of Appendix B to part
60. For flares that routinely have flow,
the owner or operator of each total
reduced sulfur monitor shall use EPA
Method 15A of Appendix A–5 to part 60
for conducting the relative accuracy
evaluations. The method ANSI/ASME
PTC 19.10–1981 (incorporated by
reference-see § 60.17) is an acceptable
alternative to EPA Method 15A of
Appendix A–5 to part 60. The
alternative relative accuracy procedures
described in section 16.0 of Performance
Specification 2 of Appendix B to part 60
(cylinder gas audits) may be used for
conducting the relative accuracy
evaluations. For flares that do not
receive routine flow, the alternative
relative accuracy procedures described
in section 16.0 of Performance
Specification 2 of Appendix B to part 60
(cylinder gas audits) may be used for
conducting the relative accuracy
evaluations, except that it is not
necessary to include as much of the
sampling probe or sampling line as
practical.
(iii) The owner or operator shall
comply with the applicable quality
assurance procedures in Appendix F to
part 60 for each total reduced sulfur
monitor.
(2) H2S monitoring requirements. The
owner or operator shall install, operate,
calibrate, and maintain an instrument
for continuously monitoring and
recording the concentration of H2S in
gas discharged to the flare according to
the requirements in paragraphs (e)(2)(i)
through (iii) of this section and shall
collect and analyze samples of the gas
and calculate total sulfur concentrations
as specified in paragraphs (e)(2)(iv)
through (ix) of this section.
(i) The owner or operator shall install,
operate and maintain each H2S monitor
according to Performance Specification
7 of Appendix B to part 60. The span
value should be determined based on
the maximum sulfur content of gas that
can be discharged to the flare (e.g.,
roughly 1.1 to 1.3 times the maximum
anticipated sulfur concentration), but
may be no less than 5,000 ppmv. A
single dual range H2S monitor may be
used to comply with the requirements of
this paragraph and paragraph (a)(2) of
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56477
sulfur using either EPA Method 15A of
Appendix A–5 to part 60, EPA Method
16A of Appendix A–6 to part 60, ASTM
Method D4468–85 (Reapproved 2006)
(incorporated by reference—see § 60.17)
or ASTM Method D5504–08
(incorporated by reference—see § 60.17).
(vi) The owner or operator shall
develop a 10-day average total sulfur-toH2S ratio and 95-percent confidence
interval as follows:
(A) Calculate the ratio of the total
sulfur concentration to the H2S
concentration for each day during
which samples are collected.
(B) Determine the 10-day average total
sulfur-to-H2S ratio as the arithmetic
average of the daily ratios calculated in
paragraph (e)(2)(vi)(A) of this section.
(C) Determine the acceptable range for
subsequent weekly samples based on
the 95-percent confidence interval for
the distribution of daily ratios based on
the 10 individual daily ratios using
Equation 11 of this section.
Where:
AR = Acceptable range of subsequent ratio
determinations, unitless.
RatioAvg = 10-day average total sulfur-to-H2S
concentration ratio, unitless.
2.262 = t-distribution statistic for 95-percent
2-sided confidence interval for 10
samples (9 degrees of freedom).
SDev = Standard deviation of the 10 daily
average total sulfur-to-H2S concentration
ratios used to develop the 10-day average
total sulfur-to-H2S concentration ratio,
unitless.
(viii) For all days other than those
during which data are being collected to
develop a 10-day average, the owner or
operator shall multiply the most recent
10-day average total sulfur-to-H2S ratio
by the daily average H2S concentrations
obtained using the monitor as required
by paragraph (e)(2)(i) through (iii) of this
section to estimate total sulfur
concentrations.
(ix) If the total sulfur-to-H2S ratio for
a subsequent weekly sample is outside
the acceptable range for the most recent
distribution of daily ratios, the owner or
operator shall develop a new 10-day
average ratio and acceptable range based
on data for the outlying weekly sample
plus data collected over the following 9
operating days.
(3) SO2 monitoring requirements. The
owner or operator shall install, operate,
calibrate and maintain an instrument for
continuously monitoring and recording
the concentration of SO2 from a process
heater or other fuel gas combustion
device that is combusting gas
representative of the fuel gas in the flare
gas line according to the requirements
in paragraph (a)(1) of this section,
determine the F factor of the fuel gas at
least daily according to the
requirements in paragraphs (d)(2)
through (4) of this section, determine
the higher heating value of the fuel gas
at least daily according to the
requirements in paragraph (d)(7) of this
section and calculate the total sulfur
content (as SO2) in the fuel gas using
Equation 12 of this section.
(iv) of this section are exempt from the
requirements in paragraphs (e)(1)
through (3) of this section. For each
such flare, except as provided in
paragraph (e)(4)(iv), engineering
calculations shall be used to calculate
the SO2 emissions in the event of a
discharge that may trigger a root cause
analysis under § 60.103a(c)(1).
(i) Flares that can only receive:
(A) Fuel gas streams that are
inherently low in sulfur content as
described in paragraph (a)(3)(i) through
(iv) of this section; and/or
(B) Fuel gas streams that are
inherently low in sulfur content for
which the owner or operator has
applied for an exemption from the H2S
monitoring requirements as described in
paragraph (b) of this section.
(ii) Emergency flares, provided that
for each such flare, the owner or
operator complies with the monitoring
alternative in paragraph (g) of this
section.
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(vii) For each day during the period
when data are being collected to
develop a 10-day average, the owner or
operator shall estimate the total sulfur
concentration using the measured total
sulfur concentration measured for that
day.
Where:
TSFG = Total sulfur concentration, as SO2, in
the fuel gas, ppmv.
CSO2 = Concentration of SO2 in the exhaust
gas, ppmv (dry basis at 0-percent excess
air).
Fd = F factor gas on dry basis at 0-percent
excess air, dscf/MMBtu.
HHVFG = Higher heating value of the fuel gas,
MMBtu/scf.
(4) Exemptions from sulfur
monitoring requirements. Flares
identified in paragraphs (e)(4)(i) through
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ER12SE12.010
in section 16.0 of Performance
Specification 2 of Appendix B to part 60
(cylinder gas audits) may be used for
conducting the relative accuracy
evaluations, except that it is not
necessary to include as much of the
sampling probe or sampling line as
practical.
(iii) The owner or operator shall
comply with the applicable quality
assurance procedures in Appendix F to
part 60 for each H2S monitor.
(iv) In the first 10 operating days after
the date the flare must begin to comply
with § 60.103a(c)(1), the owner or
operator shall collect representative
daily samples of the gas discharged to
the flare. The samples may be grab
samples or integrated samples. The
owner or operator shall take subsequent
representative daily samples at least
once per week or as required in
paragraph (e)(2)(ix) of this section.
(v) The owner or operator shall
analyze each daily sample for total
ER12SE12.009
this section provided the applicable
span specifications are met.
(ii) The owner or operator shall
conduct performance evaluations of
each H2S monitor according to the
requirements in § 60.13(c) and
Performance Specification 7 of
Appendix B to part 60. For flares that
routinely have flow, the owner or
operator shall use EPA Method 11, 15 or
15A of Appendix A–5 to part 60 for
conducting the relative accuracy
evaluations. The method ANSI/ASME
PTC 19.10–1981 (incorporated by
reference—see § 60.17) is an acceptable
alternative to EPA Method 15A of
Appendix A–5 to part 60. The
alternative relative accuracy procedures
described in section 16.0 of Performance
Specification 2 of Appendix B to part 60
(cylinder gas audits) may be used for
conducting the relative accuracy
evaluations. For flares that do not
receive routine flow, the alternative
relative accuracy procedures described
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
(iii) Flares equipped with flare gas
recovery systems designed, sized and
operated to capture all flows except
those resulting from startup, shutdown
or malfunction, provided that for each
such flare, the owner or operator
complies with the monitoring
alternative in paragraph (g) of this
section.
(iv) Secondary flares that receive gas
diverted from the primary flare. In the
event of a discharge from the secondary
flare, the sulfur content measured by the
sulfur monitor on the primary flare
should be used to calculate SO2
emissions, regardless of whether or not
the monitoring alternative in paragraph
(g) of this section is selected for the
secondary flare.
(f) Flow monitoring for flares. Except
as provided in paragraphs (f)(2) and (h)
of this section, the owner or operator of
an affected flare subject to § 60.103a(c)
through (e) shall install, operate,
calibrate and maintain, in accordance
with the specifications in paragraph
(f)(1) of this section, a CPMS to measure
and record the flow rate of gas
discharged to the flare. If a flow monitor
is not already in place, the owner or
operator of a modified flare shall
comply with the requirements of this
paragraph by no later than November
11, 2015 or upon startup of the modified
flare, whichever is later.
(1) The owner or operator shall
install, calibrate, operate and maintain
each flow monitor according to the
manufacturer’s procedures and
specifications and the following
requirements.
(i) Locate the monitor in a position
that provides a representative
measurement of the total gas flow rate.
(ii) Use a flow sensor with a
measurement sensitivity of no more
than 5 percent of the flow rate or 10
cubic feet per minute, whichever is
greater.
(iii) Use a flow monitor that is
maintainable online, is able to
continuously correct for temperature
and pressure and is able to record flow
in standard conditions (as defined in
§ 60.2) over one-minute averages.
(iv) At least quarterly, perform a
visual inspection of all components of
the monitor for physical and operational
integrity and all electrical connections
for oxidation and galvanic corrosion if
the flow monitor is not equipped with
a redundant flow sensor.
(v) Recalibrate the flow monitor in
accordance with the manufacturer’s
procedures and specifications biennially
(every two years) or at the frequency
specified by the manufacturer.
(2) Emergency flares, secondary flares
and flares equipped with flare gas
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recovery systems designed, sized and
operated to capture all flows except
those resulting from startup, shutdown
or malfunction are not required to
install continuous flow monitors;
provided, however, that for any such
flare, the owner or operator shall
comply with the monitoring alternative
in paragraph (g) of this section.
(g) Alternative monitoring for certain
flares equipped with water seals. The
owner or operator of an affected flare
subject to § 60.103a(c) through (e) that
can be classified as either an emergency
flare, a secondary flare or a flare
equipped with a flare gas recovery
system designed, sized and operated to
capture all flows except those resulting
from startup, shutdown or malfunction
may, as an alternative to the sulfur and
flow monitoring requirements of
paragraphs (e) and (f) of this section,
install, operate, calibrate and maintain,
in accordance with the requirements in
paragraphs (g)(1) through (7) of this
section, a CPMS to measure and record
the pressure in the flare gas header
between the knock-out pot and water
seal and to measure and record the
water seal liquid level. If the required
monitoring systems are not already in
place, the owner or operator of a
modified flare shall comply with the
requirements of this paragraph by no
later than November 11, 2015 or upon
startup of the modified flare, whichever
is later.
(1) Locate the pressure sensor(s) in a
position that provides a representative
measurement of the pressure and locate
the liquid seal level monitor in a
position that provides a representative
measurement of the water column
height.
(2) Minimize or eliminate pulsating
pressure, vibration and internal and
external corrosion.
(3) Use a pressure sensor and level
monitor with a minimum tolerance of
1.27 centimeters of water.
(4) Using a manometer, check
pressure sensor calibration quarterly.
(5) Conduct calibration checks any
time the pressure sensor exceeds the
manufacturer’s specified maximum
operating pressure range or install a new
pressure sensor.
(6) In a cascaded flare system that
employs multiple secondary flares,
pressure and liquid level monitoring is
required only on the first secondary
flare in the system (i.e., the secondary
flare with the lowest pressure release set
point).
(7) This alternative monitoring option
may be elected only for flares with four
or fewer pressure exceedances required
to be reported under § 60.108a(d)(5)
(‘‘reportable pressure exceedances’’) in
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any 365 consecutive calendar days.
Following the fifth reportable pressure
exceedance in a 365-day period, the
owner or operator must comply with the
sulfur and flow monitoring
requirements of paragraphs (e) and (f) of
this section as soon as practical, but no
later than 180 days after the fifth
reportable pressure exceedance in a 365day period.
(h) Alternative monitoring for flares
located in the BAAQMD or SCAQMD.
An affected flare subject to this subpart
located in the BAAQMD may elect to
comply with the monitoring
requirements in both BAAQMD
Regulation 12, Rule 11 and BAAQMD
Regulation 12, Rule 12 as an alternative
to complying with the requirements of
paragraphs (e) and (f) of this section. An
affected flare subject to this subpart
located in the SCAQMD may elect to
comply with the monitoring
requirements in SCAQMD Rule 1118 as
an alternative to complying with the
requirements of paragraphs (e) and (f) of
this section.
(i) Excess emissions. For the purpose
of reports required by § 60.7(c), periods
of excess emissions for fuel gas
combustion devices subject to the
emissions limitations in § 60.102a(g)
and flares subject to the concentration
requirement in § 60.103a(h) are defined
as specified in paragraphs (i)(1) through
(5) of this section. Determine a rolling
3-hour or a rolling daily average as the
arithmetic average of the applicable 1hour averages (e.g., a rolling 3-hour
average is the arithmetic average of
three contiguous 1-hour averages).
Determine a rolling 30-day or a rolling
365-day average as the arithmetic
average of the applicable daily averages
(e.g., a rolling 30-day average is the
arithmetic average of 30 contiguous
daily averages).
(1) SO 2 or H2S limits for fuel gas
combustion devices. (i) If the owner or
operator of a fuel gas combustion device
elects to comply with the SO2 emission
limits in § 60.102a(g)(1)(i), each rolling
3-hour period during which the average
concentration of SO2 as measured by the
SO2 continuous monitoring system
required under paragraph (a)(1) of this
section exceeds 20 ppmv, and each
rolling 365-day period during which the
average concentration of SO2 as
measured by the SO2 continuous
monitoring system required under
paragraph (a)(1) of this section exceeds
8 ppmv.
(ii) If the owner or operator of a fuel
gas combustion device elects to comply
with the H2S concentration limits in
§ 60.102a(g)(1)(ii), each rolling 3-hour
period during which the average
concentration of H2S as measured by the
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Federal Register / Vol. 77, No. 177 / Wednesday, September 12, 2012 / Rules and Regulations
H2S continuous monitoring system
required under paragraph (a)(2) of this
section exceeds 162 ppmv and each
rolling 365-day period during which the
average concentration as measured by
the H2S continuous monitoring system
under paragraph (a)(2) of this section
exceeds 60 ppmv.
(iii) If the owner or operator of a fuel
gas combustion device becomes subject
to the requirements of daily stain tube
sampling in paragraph (b)(3)(iii) of this
section, each day during which the
daily concentration of H2S exceeds 162
ppmv and each rolling 365-day period
during which the average concentration
of H2S exceeds 60 ppmv.
(2) H2S concentration limits for flares.
(i) Each rolling 3-hour period during
which the average concentration of H2S
as measured by the H2S continuous
monitoring system required under
paragraph (a)(2) of this section exceeds
162 ppmv.
(ii) If the owner or operator of a flare
becomes subject to the requirements of
daily stain tube sampling in paragraph
(b)(3)(iii) of this section, each day
during which the daily concentration of
H2S exceeds 162 ppmv.
(3) Rolling 30-day average NOX limits
for fuel gas combustion devices. Each
rolling 30-day period during which the
average concentration of NOX as
measured by the NOX continuous
monitoring system required under
paragraph (c) or (d) of this section
exceeds:
(i) For a natural draft process heater,
40 ppmv and, if monitored according to
§ 60.107a(d), 0.040 lb/MMBtu;
(ii) For a forced draft process heater,
60 ppmv and, if monitored according to
§ 60.107a(d), 0.060 lb/MMBtu; and
(iii) For a co-fired process heater
electing to comply with the NOX limit
in § 60.102a(g)(2)(iii)(A) or (g)(2)(iv)(A),
150 ppmv.
(iv) The site-specific limit determined
by the Administrator under § 60.102a(i).
(4) Daily NOX limits for fuel gas
combustion devices. Each day during
which the concentration of NOX as
measured by the NOX continuous
monitoring system required under
paragraph (d) of this section exceeds the
daily average emissions limit calculated
using Equation 3 in
§ 60.102a(g)(2)(iii)(B) or Equation 4 in
§ 60.102a(g)(2)(iv)(B).
(5) Daily O2 limits for fuel gas
combustion devices. Each day during
which the concentration of O2 as
measured by the O2 continuous
monitoring system required under
paragraph (c)(6) of this section exceeds
the O2 operating limit or operating curve
determined during the most recent
biennial performance test.
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18. Section 60.108a is amended by:
a. Revising paragraph (b);
b. Revising paragraph (c)(1);
c. Revising paragraph (c)(6)
introductory text and paragraphs
(c)(6)(ii) through (vi);
■ d. Adding paragraphs (c)(6)(vii), (viii),
(ix), (x) and (xi);
■ e. Adding paragraph (c)(7); and
■ f. Revising paragraph (d)(5).
The revisions and additions read as
follows:
■
■
■
■
§ 60.108a Recordkeeping and reporting
requirements.
*
*
*
*
*
(b) Each owner or operator subject to
an emissions limitation in § 60.102a
shall notify the Administrator of the
specific monitoring provisions of
§§ 60.105a, 60.106a and 60.107a with
which the owner or operator intends to
comply. Each owner or operator of a cofired process heater subject to an
emissions limitation in
§ 60.102a(g)(2)(iii) or (iv) shall submit to
the Administrator documentation
showing that the process heater meets
the definition of a co-fired process
heater in § 60.101a. Notifications
required by this paragraph shall be
submitted with the notification of initial
startup required by § 60.7(a)(3).
(c) * * *
(1) A copy of the flare management
plan.
*
*
*
*
*
(6) Records of discharges greater than
500 lb SO2 in any 24-hour period from
any affected flare, discharges greater
than 500 lb SO2 in excess of the
allowable limits from a fuel gas
combustion device or sulfur recovery
plant and discharges to an affected flare
in excess of 500,000 scf above baseline
in any 24-hour period as required by
§ 60.103a(c). If the monitoring
alternative provided in § 60.107a(g) is
selected, the owner or operator shall
record any instance when the flare gas
line pressure exceeds the water seal
liquid depth, except for periods
attributable to compressor staging that
do not exceed the staging time specified
in § 60.103a(a)(3)(vii)(C). The following
information shall be recorded no later
than 45 days following the end of a
discharge exceeding the thresholds:
*
*
*
*
*
(ii) The date and time the discharge
was first identified and the duration of
the discharge.
(iii) The measured or calculated
cumulative quantity of gas discharged
over the discharge duration. If the
discharge duration exceeds 24 hours,
record the discharge quantity for each
24-hour period. For a flare, record the
measured or calculated cumulative
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56479
quantity of gas discharged to the flare
over the discharge duration. If the
discharge duration exceeds 24 hours,
record the quantity of gas discharged to
the flare for each 24-hour period.
Engineering calculations are allowed for
fuel gas combustion devices, but are not
allowed for flares, except for those
complying with the alternative
monitoring requirements in § 60.107a(g).
(iv) For each discharge greater than
500 lb SO2 in any 24-hour period from
a flare, the measured total sulfur
concentration or both the measured H2S
concentration and the estimated total
sulfur concentration in the fuel gas at a
representative location in the flare inlet.
(v) For each discharge greater than
500 lb SO2 in excess of the applicable
short-term emissions limit in
§ 60.102a(g)(1) from a fuel gas
combustion device, either the measured
concentration of H2S in the fuel gas or
the measured concentration of SO2 in
the stream discharged to the
atmosphere. Process knowledge can be
used to make these estimates for fuel gas
combustion devices, but cannot be used
to make these estimates for flares,
except as provided in § 60.107a(e)(4).
(vi) For each discharge greater than
500 lb SO2 in excess of the allowable
limits from a sulfur recovery plant,
either the measured concentration of
reduced sulfur or SO2 discharged to the
atmosphere.
(vii) For each discharge greater than
500 lb SO2 in any 24-hour period from
any affected flare or discharge greater
than 500 lb SO2 in excess of the
allowable limits from a fuel gas
combustion device or sulfur recovery
plant, the cumulative quantity of H2S
and SO2 released into the atmosphere.
For releases controlled by flares, assume
99-percent conversion of reduced sulfur
or total sulfur to SO2. For fuel gas
combustion devices, assume 99-percent
conversion of H2S to SO2.
(viii) The steps that the owner or
operator took to limit the emissions
during the discharge.
(ix) The root cause analysis and
corrective action analysis conducted as
required in § 60.103a(d), including an
identification of the affected facility, the
date and duration of the discharge, a
statement noting whether the discharge
resulted from the same root cause(s)
identified in a previous analysis and
either a description of the recommended
corrective action(s) or an explanation of
why corrective action is not necessary
under § 60.103a(e).
(x) For any corrective action analysis
for which corrective actions are required
in § 60.103a(e), a description of the
corrective action(s) completed within
the first 45 days following the discharge
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and, for action(s) not already completed,
a schedule for implementation,
including proposed commencement and
completion dates.
(xi) For each discharge from any
affected flare that is the result of a
planned startup or shutdown of a
refinery process unit or ancillary
equipment connected to the affected
flare, a statement that a root cause
analysis and corrective action analysis
are not necessary because the owner or
operator followed the flare management
plan.
(7) If the owner or operator elects to
comply with § 60.107a(e)(2) for a flare,
records of the H2S and total sulfur
analyses of each grab or integrated
sample, the calculated daily total sulfurto-H2S ratios, the calculated 10-day
average total sulfur-to-H2S ratios and the
95-percent confidence intervals for each
10-day average total sulfur-to-H2S ratio.
(d) * * *
(5) The information described in
paragraph (c)(6) of this section for all
discharges listed in paragraph (c)(6) of
this section. For a flare complying with
the monitoring alternative under
§ 60.107a(g), following the fifth
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discharge required to be recorded under
paragraph (c)(6) of this section and
reported under this paragraph, the
owner or operator shall include
notification that monitoring systems
will be installed according to
§ 60.107a(e) and (f) within 180 days
following the fifth discharge.
*
*
*
*
*
■ 19. Section 60.109a is amended by
revising paragraph (b) introductory text
and adding paragraph (b)(4) to read as
follows:
§ 60.109a
Delegation of authority.
*
*
*
*
*
(b) In delegating implementation and
enforcement authority of this subpart to
a state, local or tribal agency, the
approval authorities contained in
paragraphs (b)(1) through (4) of this
section are retained by the
Administrator of the U.S. EPA and are
not transferred to the state, local or
tribal agency.
*
*
*
*
*
(4) Approval of an application for an
alternative means of emission limitation
under § 60.103a(j) of this subpart.
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Fmt 4701
Sfmt 9990
20. Table 1 to subpart Ja is added to
read as follows:
■
TABLE 1 TO SUBPART JA OF PART
60—MOLAR EXHAUST VOLUMES AND
MOLAR HEAT CONTENT OF FUEL
GAS CONSTITUENTS
Constituent
Methane (CH4) ..........
Ethane (C2H6) ...........
Hydrogen (H2) ...........
Ethene (C2H4) ...........
Propane (C3H8) .........
Propene (C3H6) .........
Butane (C4H10) .........
Butene (C4H8) ...........
Inerts .........................
MEVa
dscf/mol
MHCb
Btu/mol
7.29
12.96
1.61
11.34
18.62
17.02
24.30
22.69
0.85
842
1,475
269
1,335
2,100
1,947
2,717
2,558
0
a MEV = molar exhaust volume, dry standard cubic feet per gram-mole (dscf/g-mol) at
standard conditions of 68 °F and 1 atmosphere.
b MHC = molar heat content (higher heating
value basis), Btu per gram-mole (Btu/g-mol).
[FR Doc. 2012–20866 Filed 9–11–12; 8:45 am]
BILLING CODE 6560–50–P
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Agencies
[Federal Register Volume 77, Number 177 (Wednesday, September 12, 2012)]
[Rules and Regulations]
[Pages 56421-56480]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-20866]
[[Page 56421]]
Vol. 77
Wednesday,
No. 177
September 12, 2012
Part III
Environmental Protection Agency
-----------------------------------------------------------------------
40 CFR Parts 9 and 60
Standards of Performance for Petroleum Refineries; Standards of
Performance for Petroleum Refineries for Which Construction,
Reconstruction, or Modification Commenced After May 14, 2007; Final
Rule
Federal Register / Vol. 77 , No. 177 / Wednesday, September 12, 2012
/ Rules and Regulations
[[Page 56422]]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Parts 9 and 60
[EPA-HQ-OAR-2007-0011; FRL-9672-3]
RIN 2060-AN72
Standards of Performance for Petroleum Refineries; Standards of
Performance for Petroleum Refineries for Which Construction,
Reconstruction, or Modification Commenced After May 14, 2007
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule; lift stay of effective date.
-----------------------------------------------------------------------
SUMMARY: On June 24, 2008, the EPA promulgated amendments to the
Standards of Performance for Petroleum Refineries and new standards of
performance for petroleum refinery process units constructed,
reconstructed or modified after May 14, 2007. The EPA subsequently
received three petitions for reconsideration of these final rules. On
September 26, 2008, the EPA granted reconsideration and issued a stay
for the issues raised in the petitions regarding process heaters and
flares. On December 22, 2008, the EPA addressed those specific issues
by proposing amendments to certain provisions for process heaters and
flares and extending the stay of these provisions until further notice.
The EPA also proposed technical corrections to the rules for issues
that were raised in the petitions for reconsideration. In this action,
the EPA is finalizing those amendments and technical corrections and is
lifting the stay of all the provisions granted on September 26, 2008
and extended until further notice on December 22, 2008.
DATES: The stay of the definition of ``flare'' in 40 CFR 60.101a,
paragraph (g) of 40 CFR 60.102a, and paragraphs (d) and (e) of 40 CFR
60.107a is lifted and this final rule is effective on November 13,
2012. The incorporation by reference of certain publications listed in
the final rule is approved by the Director of the Federal Register as
of November 13, 2012.
ADDRESSES: The EPA has established a docket for this action under
Docket ID No. EPA-HQ-OAR-2007-0011. All documents in the docket are
listed in the www.regulations.gov index. Although listed in the index,
some information is not publicly available, e.g., confidential business
information (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 form. Publicly available docket materials are available either
electronically in www.regulations.gov or in hard copy at the EPA Docket
Center, Standards of Performance for Petroleum Refineries Docket, EPA
West Building, Room 3334, 1301 Constitution Ave. NW., Washington, DC.
The Public Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday
through Friday, excluding legal holidays. The telephone number for the
Public Reading Room is (202) 566-1744, and the telephone number for the
Air Docket is (202) 566-1742.
FOR FURTHER INFORMATION CONTACT: Ms. Brenda Shine, Office of Air
Quality Planning and Standards, Sector Policies and Programs Division,
Refining and Chemicals Group (E143-01), Environmental Protection
Agency, Research Triangle Park, NC 27711, telephone number: (919) 541-
3608; fax number: (919) 541-0246; email address: shine.brenda@epa.gov.
SUPPLEMENTARY INFORMATION: 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?
C. Judicial Review
II. Background Information
A. Executive Summary
B. Background of the Refinery NSPS
III. Summary of the Final Rules and Changes Since Proposal
A. What are the final amendments to the standards of performance
for petroleum refineries (40 CFR part 60, subpart J)?
B. What are the final amendments to the standards of performance
for process heaters (40 CFR part 60, subpart Ja)?
C. What are the final amendments to the standards of performance
for flares (40 CFR part 60, subpart Ja)?
D. What are the final amendments to the definitions in 40 CFR
part 60, subpart Ja?
E. What are the final technical corrections to 40 CFR part 60,
subpart Ja?
IV. Summary of Significant Comments and Responses
A. Process Heaters
B. Flares
C. Other Comments
V. Summary of Cost, Environmental, Energy and Economic Impacts
A. What are the emission reduction and cost impacts for the
final amendments?
B. What are the economic impacts?
C. What are the benefits?
VI. 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
D. Unfunded Mandates Reform Act
E. Executive Order 13132: Federalism
F. Executive Order 13175: Consultation and Coordination With
Indian Tribal Governments
G. Executive Order 13045: Protection of Children From
Environmental Health 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
J. Executive Order 12898: Federal Actions To Address
Environmental Justice in Minority Populations and Low-Income
Populations
K. Congressional Review Act
I. General Information
A. Does this action apply to me?
Categories and entities potentially regulated by these final rules
include:
----------------------------------------------------------------------------------------------------------------
Category NAICS Code \1\ Examples of regulated entities
----------------------------------------------------------------------------------------------------------------
Industry.................................... 32411 Petroleum refiners.
Federal government.......................... ................ Not affected.
State/local/tribal government............... ................ Not affected.
----------------------------------------------------------------------------------------------------------------
\1\ North American Industry Classification System.
This table is not intended to be exhaustive, but rather provides a
guide for readers regarding entities likely to be regulated by this
action. To determine whether your facility would be regulated by this
action, you should examine the applicability criteria in 40 CFR 60.100
and 40 CFR 60.100a. If you have any questions regarding the
applicability of this action to a particular entity, contact the person
listed in the preceding FOR FURTHER INFORMATION CONTACT section.
[[Page 56423]]
B. Where can I get a copy of this document?
In addition to being available in the docket, an electronic copy of
this final action is available on the World Wide Web (WWW) through the
Technology Transfer Network (TTN). Following signature, a copy of this
final action will be posted on the TTN's policy and guidance page for
newly proposed or promulgated rules at https://www.epa.gov/ttn/oarpg.
The TTN provides information and technology exchange in various areas
of air pollution control.
The EPA has created a redline document comparing the existing
regulatory text of 40 CFR part 60, subpart Ja and the final amendments
to aid the public's ability to understand the changes to the regulatory
text. This document has been placed in the docket for this rulemaking
(Docket ID No. EPA-HQ-OAR-2007-0011).
C. Judicial Review
Under section 307(b)(1) of the Clean Air Act (CAA), judicial review
of these final rules is available only by filing a petition for review
in the United States Court of Appeals for the District of Columbia
Circuit by November 13, 2012. Under section 307(b)(2) of the CAA, the
requirements established by these final rules may not be challenged
separately in any civil or criminal proceedings brought by the EPA to
enforce these requirements.
Section 307(d)(7)(B) of the CAA further provides that ``[o]nly an
objection to a rule or procedure which was raised with reasonable
specificity during the period for public comment (including any public
hearing) may be raised during judicial review.'' This section also
provides a mechanism for us to convene a proceeding for
reconsideration, ``[i]f the person raising an objection can demonstrate
to the EPA that it was impracticable to raise such objection within
[the period for public comment] or if the grounds for such objection
arose after the period for public comment (but within the time
specified for judicial review) and if such objection is of central
relevance to the outcome of the rule.'' Any person seeking to make such
a demonstration to us should submit a Petition for Reconsideration to
the Office of the Administrator, U.S. EPA, Room 3000, Ariel Rios
Building, 1200 Pennsylvania Ave. NW., Washington, DC 20460, with a copy
to both the person(s) listed in the preceding FOR FURTHER INFORMATION
CONTACT section, and the Associate General Counsel for the Air and
Radiation Law Office, Office of General Counsel (Mail Code 2344A), U.S.
EPA, 1200 Pennsylvania Ave. NW., Washington, DC 20460.
II. Background Information
A. Executive Summary
1. Purpose of the Regulatory Action
This action finalizes amendments that were proposed on December 22,
2008, to address reconsideration issues related to the promulgation of
new source performance standards (NSPS) for flares and process heaters
on June 24, 2008. This action also lifts the stay that was granted on
September 26, 2008 (73 FR 55751) and extended until further notice on
December 22, 2008 (73 FR 78552) on the provisions at issue.
2. Summary of Major Provisions
Table 1 presents a summary of major changes to the rule since it
was first promulgated on June 24, 2008. The following discussion is a
summary of major provisions of this rule.
Table 1--Summary of Major Changes Since June 24, 2008, Promulgation
----------------------------------------------------------------------------------------------------------------
Affected source Aspect NSPS Ja (June 24, 2008) NSPS Ja final
----------------------------------------------------------------------------------------------------------------
All Process Heater NOX limits........ Averaging time......... 24-hour rolling average 30-day rolling average.
Natural Draft Process Heaters........ NOX Emission Limits.... 40 ppmv................ 40 ppmv or 0.04 lb/MM
BTU.
Forced Draft Process Heaters......... NOX Emission Limits.... 40 ppmv................ 60 ppmv or 0.06 lb/MM
BTU.
Forced Draft Process Heaters with Co- NOX Emission Limits.... 40 ppmv................ 150 ppmv or Weighted
fired (oil and gas) Burners. average based on oil
at 0.40 lb/MM BTU and
gas at 0.11 lb/MM BTU.
Natural Draft Process Heaters with Co- NOX Emission Limits.... 40 ppmv................ 150 ppmv or weighted
fired (oil and gas) Burners. average based on oil
at 0.35 lb/MM BTU and
gas at 0.06 lb/MM BTU.
Process Heaters...................... Alternate Emission None................... Case by case approval
Standards. for some
circumstances.
Flares............................... Applicability.......... New or reconstructed Similar, except
flare systems or specific list of
existing flare systems connections that do
that are physically not trigger
altered to increase applicability.
flow or to add new
connections.
Fuel gas combustion devices.......... H2S concentration limit 162 ppmv H2S (3-hour 162 ppmv H2S (3-hour
average); 60 ppmv H2S average); No 60 ppmv
(annual rolling H2S long term
average). concentration limit
for flares.
Flares............................... Compliance date for Comply with H2S limit Comply with H2S limit
modified flares. at start-up, and all at start-up (except
other requirements for modified flares
within 1 year. not previously subject
to the H2S limit in 40
CFR part 60, subpart J
or those with
monitoring
alternatives, or those
complying with subpart
J as specified in a
consent decree, which
comply no later than 3
years) and all other
requirements within 3
years.
Flares............................... Flow limits............ Flare system-wide flow No limits.
limit of 250,000 scfd.
[[Page 56424]]
Flares............................... Root Cause Analysis and RCA/CA required on RCA/CA required for
Corrective Action (RCA/ upsets or malfunctions 500,000 scfd above
CA). in excess of 500,000 base load and 500 lbs
scfd or 500 lbs/day SO2 in any 24-hour
SO2 from SSM. period.
Flares............................... Flow monitoring........ Continuous............. Continuous except for
intermittent/emergency
only flares with water
seal monitoring and
limited releases.
Flares............................... Sulfur Monitoring...... Continuous Total Continuous TRS, using
Reduced Sulfur (TRS). reference method 15A
(Total Sulfur).
----------------------------------------------------------------------------------------------------------------
Affected process heaters are those that were modified,
reconstructed or constructed after May 14, 2007. For these affected
sources, these final amendments include concentration-based nitrogen
oxide (NOX) emissions limits and alternative heating value-
based NOX emissions limits, both determined daily on a 30-
day rolling average basis. These final amendments establish limits of
40 parts per million by volume (ppmv) NOX (or 0.04 pounds
per million British thermal units (lb/MMBtu) and 60 ppmv NOX
(or 0.06 lb/MMBtu) for natural draft and forced draft process heaters,
respectively. Co-fired process heaters, designed to operate on gaseous
and liquid fuel (e.g., oil), must meet either 150 ppmv NOX
or alternative heating value-based limits, weighted based on oil and
gas use. The NSPS also contains an alternative compliance option that
allows owners and operators to obtain EPA approval for a site-specific
NOX limit for process heaters that may have difficulty
meeting the standards under certain situations. These final amendments
also include monitoring, recordkeeping and reporting requirements
necessary to demonstrate compliance with the NOX emission
standards.
For flares, these final amendments define a flare as a separate
affected facility rather than a type of fuel gas combustion device. As
such, these final amendments remove requirements for flares to comply
with the performance standards for sulfur dioxide (SO2)
(expressed as a 162 ppmv short-term hydrogen sulfide (H2S)
concentration limit) and, instead, establish a separate suite of
standards for flares. We are not finalizing the requirement in the
December 22, 2008, proposed amendments for flares to meet the long-term
60 ppmv H2S fuel gas concentration limit. As explained in
section IV of this preamble, we determined that requiring refineries to
ensure the fuel gas they send to their flares meets a long-term
H2S concentration of 60 ppmv is not appropriate for flares.
Affected flares are those that were modified, reconstructed or
constructed after June 24, 2008. In general, a flare is modified if a
connection is made into the flare header that can increase emissions
from the flare. The NSPS specifically identifies certain connections to
a flare that do not constitute a modification of the flare because they
do not result in emissions increases.
The final amendments for flares include a suite of standards that
apply at all times. This suite of standards requires refineries to: (1)
Develop and implement a flare management plan; (2) conduct root cause
analyses and take corrective action when waste gas sent to the flare
exceeds a flow rate of 500,000 standard cubic feet per day (scfd) above
the baseline flow or contains sulfur that, upon combustion, will emit
more than 500 pounds (lb) of SO2 in a 24-hour period; and
(3) optimize management of the fuel gas by limiting the short-term
concentration of H2S to 162 ppmv during normal operating
conditions.
The final amendments require that flares be equipped with flow and
sulfur monitors except in cases where flares are used infrequently or
are configured such that they cannot receive high sulfur gas. For
flares that are configured such that they only receive inherently low
sulfur gas streams, continuous sulfur monitors are not necessary
because a root cause analysis will be triggered by an exceedance of the
flow rate threshold long before they exceed the 500 lb SO2
trigger in a 24-hour period.
For infrequently used flares, the NSPS allows for less burdensome
monitoring, consisting of monitoring the differential pressure between
the flare header and the flare water seal to determine if a gas release
to the flare has occurred. Any instance where the pressure upstream of
the water seal (expressed in inches of water) exceeds the water seal
height triggers a requirement to perform a root cause analysis and
corrective action analysis, unless the discharge is related to flare
gas recovery system compressor cycling or a planned startup or shutdown
(of a refinery process unit or ancillary equipment connected to the
flare) following the procedures in the flare management plan. The NSPS
also contains an alternative compliance option for refinery flares
located in the South Coast Air Quality Management District (SCAQMD) or
the Bay Area Air Quality Management District (BAAQMD). An affected
flare subject to 40 CFR part 60, subpart Ja may elect to comply with
SCAQMD Rule 1118 or both BAAQMD Regulation 12, Rule 11 and BAAQMD
Regulation 12, Rule 12 as an alternative to complying with the
requirements of subpart Ja.
3. Costs and Benefits
The provisions for flares and other fuel gas combustion devices
(i.e., process heaters and boilers) from the final June 2008 standards
were stayed. The analysis for this final rule includes the same unit
costs for the flare provisions as the final June 2008 rule but reflects
recalculated total costs using data collected in the March 2011
information collection request (ICR) to update the number of flares.
For the June 2008 standards, we estimated that 40 flares would be
affected. We now anticipate that there will be 400 affected flares that
will be subject to this final rule. Table 2 includes the recalculated
cost estimates based on the updated number of flares since 2008, broken
out by specific flare requirements. For the other fuel gas combustion
devices, the total annualized costs for those provisions were estimated
at $24 million (2006 dollars) in the June 2008 rule and remain the
same. As discussed below, because there are no additional incremental
costs associated with the other fuel gas combustion device provisions,
we consider those annual costs accounted for in the final June 2008
standards. We are presenting these
[[Page 56425]]
costs and benefits here again, even though we estimate no changes to
them, since these provisions will become effective upon this final
action to lift the stay on certain provisions in the June 2008 rule.
For the June 2008 rule, we estimated the benefits to be $220 million to
$1.9 billion and $200 to $1.7 billion at a 3-percent discount rate and
7-percent discount rate, respectively.\1\
---------------------------------------------------------------------------
\1\ It is important to note that the EPA has implemented several
substantial changes to the benefits methodology since 2008, which
makes it challenging to compare the benefits of the June 2008 rule
to the benefits of the current rulemaking. The changes with the
largest impact on the range of monetized benefits are the removal of
the assumption of a threshold in the concentration-response
function, the revision of the value-of-a-statistical-life, and the
range of risk estimates from epidemiology studies rather than the
range of risk estimates supplied by experts. See the regulatory
impact analysis for the current rulemaking for more information
regarding these changes, which is available in the docket.
---------------------------------------------------------------------------
Cost impacts for flares are presented in Table 2. The estimated
total capital cost of complying with the final amendments to 40 CFR
part 60, subpart Ja for flares is $460 million dollars (2006 dollars).
The estimated annual cost, including annualized capital costs, is a
cost savings of about $79 million (2006 dollars) due to the replacement
of some natural gas purchases with recovered flare gas and the
retention of intermediate and product streams due to a reduction in the
number of malfunctions associated with refinery process units and
ancillary equipment connected to the flare. Note that not all refiners
will realize a cost savings since we only estimate that refineries with
high flare flows will install vapor recovery systems. Although the rule
does not specifically require installation of flare gas recovery
systems, we project that owners and operators of flares receiving high
waste gas flows will conclude, upon installation of monitors,
implementation of their flare management plans, and implementation of
root causes analyses, that installing flare gas recovery would result
in fuel savings by using the recovered flare gas where purchased
natural gas is now being used to fire equipment such as boilers and
process heaters. The flare management plan requires refiners to conduct
a thorough review of the flare system so that flare gas recovery
systems are installed and used where these systems are warranted. As
part of the development of the flare management plan, refinery owners
and operators must provide rationale and supporting evidence regarding
the flare waste gas reduction options considered. In addition,
consistent with Executive Order 13563 (Improving Regulation and
Regulatory Review, issued on January 18, 2011), for facilities
implementing flare gas recovery, we are finalizing provisions that
would allow the owner or operator to reduce monitoring costs and the
number of root cause analyses, corrective actions, and corresponding
recordkeeping and reporting they would need to perform. The costs
calculated for this rule, however, do not account for potential savings
due to these provisions (reduced monitoring, root cause analysis,
etc.). We estimate that the final requirements for flares will reduce
emissions of SO2 by 3,200 tons per year (tons/yr),
NOX by 1,100 tons/yr and volatile organic compounds (VOC) by
3,400 tons/yr from the baseline. The overall cost effectiveness is a
cost savings of about $10,000 per ton of combined pollutants removed.
We also estimate that the final requirements for flares will result in
emissions reduction co-benefits of CO2 equivalents by
1,900,000 metric tonnes per year, predominantly as a result of our
estimate of the largest flares employing flare gas recovery, and to a
lesser extent, as a result of the flow rate root cause analyses and
corrective actions applicable to all flares.
Table 2--Cost Impacts for Petroleum Refinery Flares Subject to Amended Standards Under 40 CFR Part 60, Subpart Ja
[Fifth year after the effective date of these final rule amendments]
--------------------------------------------------------------------------------------------------------------------------------------------------------
Natural gas Annual Annual Annual Cost
Total Total annual offset/product Total annual emission emission emission effectiveness
Subpart Ja requirements capital cost cost without recovery cost ($1,000/ reductions reductions reductions ($/ton
($1,000) credit credit yr) (tons SO2/ (tons NOX/ (tons VOC/ emissions
($1,000/yr) ($1,000) yr) yr) yr) reduced)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Majority of flares (approximately 360 flares)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Flare Monitoring.................. 72,000 12,000 0 12,000 0 0 0 ..............
Flare gas recovery................ 0 0 0 0 0 0 0 ..............
Flare Management.................. 0 790 0 790 0 0 270 2,900
SO2 RCA/CA........................ 0 1,900 0 1,900 2,600 0 0 760
Flowrate RCA/CA................... ............ 900 (6,700) (5,800) 3.4 50 390 (13,000)
---------------------------------------------------------------------------------------------------------------------
Subtotal \1\.................. 72,000 16,000 (6,700) 9,000 2,600 50 660 2,700
--------------------------------------------------------------------------------------------------------------------------------------------------------
Largest flares (approximately 40 flares) \2\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Flare Monitoring.................. 12,000 2,000 0 2,000 0 0 0 ..............
Flare gas recovery................ 380,000 78,000 (170,000) (90,000) 380 1,100 2,700 (22,000)
Flare Management.................. 0 88 0 88 0 0 30 2,900
SO2 RCA/CA........................ 0 220 0 220 290 0 0 760
Flowrate RCA/CA................... 0 100 (740) (640) 0.4 6 43 (13,000)
---------------------------------------------------------------------------------------------------------------------
Subtotal \1\.................. 390,000 81,000 (170,000) (88,000) 660 1,100 2,800 (20,000)
---------------------------------------------------------------------------------------------------------------------
Total \1\................. 460,000 96,000 (180,000) (79,000) 3,200 1,100 3,400 (10,000)
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ All estimates are rounded to two significant figures so numbers may not sum down columns.
\2\ The EPA has conducted an alternative analysis that presents the costs and benefits of the rule assuming that no refiners will opt to install flare
gas recovery systems as part of their flare management strategy. This analysis is presented in the Regulatory Impact Analysis in the discussion
provided in the executive summary and in Section 4.1, available in the docket for this rulemaking.
We estimate the monetized benefits of this final regulatory action
for all flares to be $260 million to $580 million (3-percent discount
rate) and $240 million to $520 million (7-percent discount rate for
health benefits and 3-percent discount rate for climate benefits). For
small flares only, we estimate the monetized benefits are $170 million
to $410 million (3-percent discount rate) and $150 million to $370
million (7-percent discount rate for health benefits
[[Page 56426]]
and 3-percent discount rate for climate benefits). For large flares
only, we estimate the monetized benefits are $93 million to $160
million (3-percent discount rate) and $88 million to $150 million (7-
percent discount rate for health benefits and 3-percent discount rate
for climate benefits). Several benefits categories, including direct
exposure to SO2 and NOX benefits, ozone benefits,
ecosystem benefits and visibility benefits are not included in these
monetized benefits. All estimates are in 2006 dollars for the year
2017.
Although this final rule provides refiners with some additional
compliance options and removes some requirements, such as the long-term
H2S limit for flares, the cost savings due this increased
flexibility have not been calculated for inclusion in the benefit-cost
analysis.
B. Background of the Refinery NSPS
Section 111(b)(1)(A) of the Clean Air Act (CAA) requires the EPA to
establish federal standards of performance for new, modified and
reconstructed sources for source categories which cause or contribute
significantly to air pollution which may reasonably be anticipated to
endanger public health or welfare. The standard of performance must
reflect the application of the best system of emission reductions
(BSER) that (taking into consideration the cost of achieving such
emission reductions, any non-air quality health and environmental
impact and energy requirements) the Administrator determines has been
adequately demonstrated (CAA section 111(a)(1)). If it is not feasible
to prescribe or enforce a standard of performance, the Administrator
may instead promulgate a design, equipment, work practice or
operational standard, or a combination of these types of standards (CAA
section 111(h)(1)). Since 1970, the NSPS have been successful in
achieving long-term emissions reductions in numerous industries by
assuring cost-effective controls are installed on newly constructed,
reconstructed or modified sources.
The level of control prescribed by CAA section 111 historically has
been referred to as ``Best Demonstrated Technology'' or BDT. In order
to better reflect that CAA section 111 was amended in 1990 to clarify
that ``best systems'' may or may not be ``technology,'' the EPA is now
using the term ``best system of emission reduction'' or BSER in its
rulemaking packages. See, e.g., 76 FR 52738, 52740 (August 23, 2011);
76 FR 63878, 63879 (October 14, 2011). As was done previously in
analyzing BDT, the EPA uses available information and considers the
emissions reductions achieved by the different systems available and
the costs of achieving those reductions. The EPA also considers the
``other factors'' prescribed by the statute in its BSER analysis. After
considering all of this information, the EPA then establishes the
appropriate standard representative of BSER. Sources may use whatever
system meets the standard.
Section 111(b)(1)(B) of the CAA requires the EPA to periodically
review and, as appropriate, revise the standards of performance to
reflect improvements in methods for reducing emissions. As a result of
our periodic review of the NSPS for petroleum refineries (40 CFR part
60, subpart J), we proposed amendments to the current standards of
performance and separate standards of performance for new process units
(40 CFR part 60, subpart Ja) (72 FR 27278, May 14, 2007) and we
subsequently promulgated those amendments and new standards (73 FR
35838, June 24, 2008). Following promulgation, we received three
separate petitions for reconsideration from: (1) The American Petroleum
Institute (API), the National Petrochemical and Refiners Association
(NPRA) and the Western States Petroleum Association (WSPA)
(collectively referred to as ``Industry Petitioners''); (2) HOVENSA,
LLC (``HOVENSA''); and (3) the Environmental Integrity Project, Sierra
Club and Natural Resources Defense Council (collectively referred to as
``Environmental Petitioners''). On September 26, 2008, the EPA issued a
Federal Register notice (73 FR 55751) granting reconsideration of the
following issues: (1) The newly promulgated flare modification
provision\2\; (2) the ``flare'' definition; (3) the fuel gas combustion
device sulfur limits as they apply to flares; (4) the flow limit for
flares; (5) the total reduced sulfur and flow monitoring requirements
for flares; and (6) the NOX limit for process heaters. The
EPA also granted Industry Petitioners' and HOVENSA's request for a 90-
day stay for those same provisions under reconsideration. On December
22, 2008, three Federal Register notices (73 FR 78260, 73 FR 78546 and
73 FR 78549) were published to extend this stay until a final decision
is reached on those issues.
---------------------------------------------------------------------------
\2\ The September 26, 2008, Federal Register notice (73 FR
55751) described the first issue for which the EPA granted
reconsideration as ``the definition of `modification.''' However,
because what we are actually reconsidering is the specific flare
modification provision that applies to flares at petroleum
refineries rather than the more generally applicable definition of
``modification,'' we have revised the description of this issue as
``the newly promulgated flare modification provision.''
---------------------------------------------------------------------------
In the September 26, 2008, Federal Register notice (73 FR 55751),
we also identified other issues for which Petitioners requested
reconsideration. We stated that, at that time, we were ``taking no
action on all of the other issues raised in the petitions but will
consider all of the outstanding issues in a future notice.'' On
December 29, 2009, we sent a letter to the Petitioners, through their
counsel, stating that ``[t]he Administrator has decided to grant
reconsideration of all the remaining issues'' and that ``EPA will
address the substantive aspects of the issues under reconsideration
through notice and comment actions published in the Federal Register.''
A copy of the letter to the Petitioners can be found in the docket for
this rulemaking (Docket Item No. EPA-HQ-OAR-2007-0011-0318).
In this action, we are finalizing the amendments for which we
granted reconsideration and a stay as outlined in the September 26,
2008, notice and for which we proposed amendments on December 22, 2008.
We are also addressing certain other minor issues raised by Industry
Petitioners in this action, as discussed later in this preamble. We
will take action on all of the remaining issues raised by Petitioners
for reconsideration in future notices.
We received a total of 22 comments from the following groups on the
proposed amendments during the public comment period: (1) Refineries,
industry trade associations and consultants; (2) state and local
environmental and public health agencies; (3) environmental groups; and
(4) other members of the public. These final amendments reflect our
full consideration of all of the comments we received. Detailed
responses to the comments not included in this preamble, as well as
more detailed summaries of the comments addressed in this preamble, are
contained in Standards of Performance for Petroleum Refineries:
Background Information for Final Amendments--Summary of Public Comments
and Responses, dated December 2011, which is included in Docket ID No.
EPA-HQ-OAR-2007-0011.
In summary, major comments on the proposed process heater
requirements were related to the proposed NOX concentration
limits, the alternative heating value limits, consideration of turndown
(i.e., when a process heater is operated at less than 50-percent design
capacity) and other factors that influence the achievable emissions
[[Page 56427]]
limits. In response, we are raising the limit for new forced draft
process heaters from 40 ppmv NOX at proposal to 60 ppmv
NOX. For both natural draft and forced draft process
heaters, we are finalizing alternative heating value limits derived
from a more direct numerical conversion of the NOX
concentration limit (i.e., 0.04 lb/MMBtu for natural draft and 0.06 lb/
MMBtu for forced draft). For newly constructed, modified and
reconstructed natural draft and forced draft process heaters, we are
reducing the averaging time for compliance from a 365-day rolling
average to a 30-day rolling average applicable during periods of normal
operation. We are also finalizing an alternative case-specific
compliance option that allows owners and operators to obtain EPA
approval for a site-specific NOX limit in certain conditions
such as turndown.
Major comments on the proposed requirements for flares were related
to the definition of flare modification for purposes of triggering
applicability to this rule, the proposed removal of the flare flow
limit, clarification of flare monitoring requirements and clarification
of the differences between the requirement for flares and the
requirements for other fuel gas combustion devices. We address these
comments by clarifying the definition of flare modification and by
expanding the list included in the December 22, 2008, proposal, which
specifies certain connections that do not constitute a modification of
the flare because they do not result in emissions increases. We are
finalizing the proposed removal of the flare flow limit and instead, we
are promulgating a suite of work practice standards that apply to
affected flares. Based on comments received on the December 22, 2008
proposal, we are finalizing definitions of ``fuel gas combustion
device'' and ``flare'' to specify that a flare is a separate affected
facility rather than a type of fuel gas combustion device. We are also
finalizing amendments to clarify certain monitoring requirements and to
provide additional monitoring alternatives under certain circumstances.
III. Summary of the Final Rules and Changes Since Proposal
NSPS for petroleum refineries (40 CFR part 60, subpart J) apply to
the affected facilities at the refinery, such as fuel gas combustion
devices (which include process heaters, boilers and flares), that
commence construction, reconstruction or modification after June 11,
1973, but on or before May 14, 2007 (on or before June 24, 2008 for
flares). The NSPS were originally promulgated on March 8, 1974, and
have been amended several times. In this action, we are promulgating
technical clarifications and corrections to subpart J.
New standards of performance for petroleum refineries (40 CFR part
60, subpart Ja) apply to flares that commence construction,
reconstruction or modification after June 24, 2008, and other affected
facilities at petroleum refineries, including process heaters and other
fuel gas combustion devices that commence construction, reconstruction
or modification after May 14, 2007. In this action, we are finalizing
amendments to subpart Ja to address the issues raised by Petitioners
regarding flares and process heaters. We are also finalizing technical
corrections to subpart Ja for certain issues that were identified by
Industry Petitioners in their August 21, 2008, supplement to their
original administrative reconsideration request (Docket Item No. EPA-
HQ-OAR-2007-0011-0246).
The following sections summarize the amendments in both 40 CFR part
60, subpart J and 40 CFR part 60, subpart Ja. Section IV contains the
rationale for these amendments, while the amendments themselves follow
the preamble.
A. What are the final amendments to the standards of performance for
petroleum refineries (40 CFR part 60, subpart J)?
The final amendments add a new paragraph to 40 CFR 60.100 to allow
40 CFR part 60, subpart J affected sources the option of complying with
subpart J by following the requirements in 40 CFR part 60, subpart Ja.
The subpart Ja requirements are at least as stringent as those in
subpart J, so providing this option will allow all process units in a
refinery to follow the same requirements and simplify compliance. We
are also removing the reference to 40 CFR 60.101a from the description
of the applicability dates in 40 CFR 60.100(b) so as not to cause
confusion over the definition of ``flare'' in subpart J. We are
finalizing a correction to the value and units (in the metric system)
for the allowable incremental rate of particulate matter (PM) emissions
in 40 CFR 60.106(c)(1). We amended the units for this constant in 40
CFR 60.102(b) on June 24, 2008, and we are now correcting 40 CFR
60.106(c)(1) accordingly. Finally, we are finalizing a definition of
``fuel gas'' that incorporates the same clarifications regarding vapors
from wastewater treatment units and marine tank vessel loading
operations identified in the subpart Ja definition of ``fuel gas''
(described later in this preamble).
B. What are the final amendments to the standards of performance for
process heaters (40 CFR part 60, subpart Ja)?
We proposed several amendments to the standards of performance for
process heaters, including adding emission limits in units of lb/MMBtu,
extending the emission limit averaging time from 24 hours to 365 days,
raising the emission limit for modified and reconstructed forced draft
process heaters and raising the emission limit for co-fired process
heaters. After consideration of all of the public comments and our own
additional analyses, we are finalizing the process heater requirements,
as described in this section.
Table 3 presents a comparison of the proposed and final 40 CFR part
60, subpart Ja amendments for process heaters. The final amendments
include four subcategories of process heaters: (1) Natural draft
process heaters; (2) forced draft process heaters; (3) co-fired natural
draft process heaters; and (4) co-fired forced draft process heaters.
At proposal, all co-fired process heaters were included in one
subcategory, for a total of three process heater subcategories, but,
based on emissions data from co-fired process heaters, we divided
natural draft and forced draft co-fired process heaters into separate
subcategories with different emissions limits.
For each of the first two subcategories, the final amendments
include a concentration-based NOX emissions limit and a
heating value-based NOX emissions limit, both determined
daily on a 30-day rolling average basis. For the natural draft process
heater subcategory, the concentration-based NOX emissions
limit for newly constructed, modified and reconstructed natural draft
process heaters is 40 ppmv (dry basis, corrected to 0-percent excess
air) determined daily on a 30-day rolling average basis. The heating
value-based NOX emissions limit for newly constructed,
modified and reconstructed natural draft process heaters is 0.040 lb/
MMBtu higher heating value basis determined daily on a 30-day rolling
average basis. The averaging time for both of these limits is shorter
than the 365-day averaging time that was proposed, and the heating
value-based NOX emissions limit differs from the proposed
limit in that it is a more direct numerical conversion from 40 ppmv
NOX. At proposal, we provided a longer averaging time so
that short periods of turndown (i.e., when a process heater is
operating at less than 50-percent design
[[Page 56428]]
capacity) would not significantly affect the overall performance of the
unit. Our analysis of the additional data that we obtained following
the proposal supported revising all NOX emissions limits to
be on a 30-day rolling average basis, which is achievable for process
heaters during periods of normal operation. These data indicate that
process heaters equipped with ultra low NOX burners meet the
emission limits described above if compliance is determined on a 30-day
rolling average basis. We are finalizing alternative compliance options
that allow the owners and operator to establish site-specific limits
applicable during certain conditions such as turndown. Section IV.A of
this preamble provides additional information regarding the rationale
and analyses leading to these final amendments.
For the second subcategory, forced draft process heaters, the
concentration-based NOX emissions limit for newly
constructed, modified and reconstructed forced draft process heaters is
60 ppmv (dry basis, corrected to 0-percent excess air) determined daily
on a 30-day rolling average basis. The heating value-based
NOX emissions limit for newly constructed, modified and
reconstructed forced draft process heaters is 0.060 lb/MMBtu higher
heating value basis determined daily on a 30-day rolling average basis.
The higher limit for new forced draft process heaters (at proposal, the
limit was 40 ppmv) is based on additional data and a re-evaluation of
BSER, as described later in this preamble. As with natural draft
process heaters, the averaging time for both of these limits is shorter
than proposed, and the final heating value-based NOX
emissions limit is a more direct numerical conversion from 60 ppmv
NOX. Section IV.A of this preamble provides additional
information regarding the rationale and analyses leading to these final
amendments.
For each of these subcategories, a process heater need only meet
either the concentration-based NOX emissions limit or the
heating value-based NOX emissions limit. The refinery owner
or operator may choose to comply with either limit at any time,
provided that they are monitoring the appropriate variables to assess
the heating value-based NOX emissions limit. If the refinery
owner or operator does not choose to monitor fuel composition, then
they must comply with the concentration-based NOX emissions
limit.
Table 3--Proposed and Final Amendments for Process Heaters
------------------------------------------------------------------------
Proposal (December
22, 2008) Final
------------------------------------------------------------------------
Averaging time.............. 365-day rolling 30-day rolling
average. average.
Natural Draft NOX Emission 40 ppmv or 0.035 lb/ 40 ppmv or 0.04 lb/
Limits. MM BTU. MM BTU.
Forced Draft NOX Emission New: 40 ppmv or 60 ppmv or 0.06 lb/
Limits. 0.035 lb/MM BTU. MM BTU.
M/R: 60 ppmv or
0.055 lb/MM BTU.
Co-fired Burner (oil and 150 ppmv or Weighted 150 ppmv or Weighted
gas) NOX Emission Limits. average based on average based on
oil at 0.27 lb/MM oil at 0.40 lb/MM
BTU and gas at 0.08 BTU and gas at 0.11
lb/MM BTU. lb/MM BTU forced
draft and weighted
average based on
oil at 0.35 lb/MM
BTU and gas at 0.06
lb/MM BTU for
natural draft.
------------------------------------------------------------------------
As proposed, initial compliance with the heating value-based
emissions limits will be demonstrated by conducting a performance
evaluation of the continuous emission monitoring system (CEMS) in
accordance with Performance Specification 2 in appendix B to 40 CFR
part 60, with EPA Method 7 of 40 CFR part 60, appendix A-4 as the
Reference Method, along with fuel flow measurements and fuel gas
compositional analysis. The NOX emission rate is calculated
using the oxygen (O2)-based F factor, dry basis according to
EPA Method 19 of 40 CFR part 60, appendix A-7. Ongoing compliance with
this NOX emissions limit is determined using a
NOX CEMS and at least daily sampling of fuel gas heat
content or composition to calculate a daily average heating value-based
emissions rate, which is subsequently used to determine the 30-day
average.
The third and fourth subcategories of process heaters are co-fired
process heaters. A co-fired process heater is a process heater that
employs burners that are designed to be supplied by both gaseous and
liquid fuels. As described in more detail in section IV.A of this
preamble, co-fired process heaters do not include gas-fired process
heaters that have emergency oil back-up burners. There are two
compliance options for each subcategory of co-fired process heaters:
(1) 150 ppmv (dry basis, corrected to 0-percent excess air) determined
daily on a 30 successive operating day rolling average basis; and (2) a
source-specific daily average emissions limit. Unlike gas-fired process
heaters, the owner or operator of a co-fired process heater must choose
one emissions limit and show compliance with that limit. For co-fired
natural draft process heaters, the daily average emissions limit is
based on a limit of 0.06 lb/MMBtu for the gas portion of the firing and
0.35 lb/MMBtu for the oil portion of the firing. For co-fired forced
draft process heaters, the daily average emissions limit is based on a
limit of 0.11 lb/MMBtu for the gas portion of the firing and 0.40 lb/
MMBtu for the oil portion of the firing. These limits are different
than proposed, based on a re-evaluation of BSER with new data received
during the public comment period. All of the requirements for emissions
monitoring, recordkeeping and reporting for co-fired process heaters
are the same as for the other process heater subcategories.
We are also finalizing an alternative compliance option that allows
owners and operators to obtain EPA approval for a site-specific
NOX limit for certain process heaters. This compliance
option was provided in the proposed amendments, but it was limited to
(1) natural draft and forced draft modified or reconstructed process
heaters that lack sufficient space to accommodate combustion
modification-based technology and (2) natural draft and forced draft
co-fired process heaters. In the final amendments, we are finalizing
this compliance option for those process heaters mentioned above while
also providing this compliance option for the following additional
types of process heaters: (3) modified or reconstructed induced draft
process heaters that have downwardly firing burners and (4) forced
draft and natural draft process heaters that operate at low firing
rates, or turndown, for an extended period of time. As we noted in the
preamble to the proposed amendments, in limited cases, existing natural
draft or forced draft process heaters have limited firebox size or
other constraints such
[[Page 56429]]
that they cannot apply the BSER of ultra-low NOX burners or
otherwise meet the applicable limit and some co-fired units may not be
able to achieve the NOX limitations even with ultra-low
NOX burner control technology. In addition, commenters noted
that downwardly fired process heaters with induced draft fans have
similar NOX control issues as forced draft heaters, but the
definition of forced draft heater does not include these induced draft
heaters (these are defined as natural draft process heaters).
Therefore, we added a provision to allow induced draft process heaters
with downwardly-firing burners to use the alternative compliance
option.
Finally, we note that the emissions limits for forced draft and
natural draft gas-fired process heaters are based on the performance of
ultra-low NOX burner control technologies. The ultra-low
NOX burner technology suppliers recommend operating with
higher excess air rates at low firing rates (at or below approximately
one-half of the maximum firing capacity), which causes higher
NOX concentrations at low firing rates. Therefore, all types
of process heaters with ultra-low NOX burner control
technologies may be unable to meet the emissions limits if they are
operated at low firing rates for an extended period of time. Requesting
a site-specific emissions limit requires a detailed demonstration that
the application of the ultra-low NOX burner technology is
not feasible or that the technology cannot meet the NOX
emissions limits given the conditions of the process heater (downward
fired induced draft, co-fired or prolonged turndown); the refinery must
also conduct source tests in developing a site-specific emissions limit
for its process heater. This analysis must be submitted to and approved
by the Administrator.
We are finalizing the proposed clarification that owners and
operators of process heaters in any subcategory with a rated heating
capacity of less than 100 million British thermal units per hour
(MMBtu/hr) have the option of using CEMS. The final rule states that
owners and operators of process heaters subject to 40 CFR part 60,
subpart Ja should use CEMS to demonstrate compliance unless the heater
is equipped with combustion modification-based technology (low-
NOX burners or ultra-low NOX burners) with a
rated heating capacity of less than 100 MMBtu/hr; owners and operators
of those specific process heaters have the alternative option of
biennial source testing to determine compliance. As requested by
commenters, we have provided additional detail in the final rule
regarding how to develop the O2 operating limit, including
provisions on how to develop an O2 operating curve to ensure
compliance with the NOX emission limit at different process
heater firing rates. We are requiring that owners and operators with
process heaters in any subcategory that are complying using biennial
source testing establish a maximum excess O2 concentration
operating limit or operating curve that can be met at all times, even
during turndown, and comply with the O2 monitoring
requirements for ongoing compliance demonstration.
C. What are the final amendments to the standards of performance for
flares (40 CFR part 60, subpart Ja)?
We proposed several amendments to the standards of performance for
flares, including, but not limited to, amending the flare modification
provision, removing the numerical limit on the flow rate to the flare,
revising the flare management plan requirements to include a list of
connections to the flare and an identification of baseline conditions,
clarifying when a root cause analysis is required, revising the sulfur
and flow monitoring requirements and providing additional time for
compliance. After consideration of all of the public comments, and our
own additional analyses, we are finalizing the flare requirements, as
described in this section.
We did not propose to revise the definitions of ``fuel gas
combustion device'' and ``flare'' on December 22, 2008. However, based
on public comment and changes to the flare requirements, as described
later in this section, we have decided to finalize revisions to these
definitions to specify that, for purposes of 40 CFR part 60, subpart
Ja, a flare is a separate affected facility rather than a type of fuel
gas combustion device. This change makes clearer the differences
between the requirements for flares and the requirements for fuel gas
combustion devices, particularly in terms of sulfur and flow rate
monitoring requirements and thresholds for root cause analyses and
corrective action analyses. We are also making corrections, as needed,
in numerous paragraphs throughout subpart Ja for consistency with the
amended definitions (e.g., adding ``and flares,'' where applicable, to
paragraphs with requirements for ``fuel gas combustion devices'').
We are finalizing the flare modification provision in 40 CFR
60.100a(c), as described below, to specify certain connections to a
flare that do not constitute a modification of the flare because they
do not result in emissions increases. On December 22, 2008, we proposed
that the following types of connections to a flare would not be
considered a modification of the flare: (1) Connections made to install
monitoring systems to the flares; (2) connections made to install a
flare gas recovery system; (3) connections made to replace or upgrade
existing pressure relief or safety valves, provided the new pressure
relief or safety valve has a set point opening pressure no lower and an
internal diameter no greater than the existing equipment being replaced
or upgraded; and (4) replacing piping or moving an existing connection
from a refinery process unit to a new location in the same flare,
provided the new pipe diameter is less than or equal to the diameter of
the pipe/connection being replaced/moved. We are finalizing those
proposed amendments and also adding the following types of connections
to the list of connections to flares that are not modifications of
flares: (1) Connections between flares; (2) connections for flare gas
sulfur removal; and (3) connections made to install redundant flare
equipment (such as a back-up compressor). We are also clarifying one of
the proposed exemptions to indicate that connections made to upgrade or
enhance components of flare gas recovery systems (e.g., additional
compressors or recycle lines) are not modifications.
We are not finalizing the proposed amendment to provide additional
time for flares that need to install additional amine scrubbing and
amine stripping columns to meet the requirement to limit the long-term
concentration of H2S to 60 ppmv (determined daily on a 365
successive calendar day rolling average basis) (hereafter referred to
as the long-term 60 ppmv H2S fuel gas concentration limit).
Instead, based on comments received during the public comment period
for the proposed amendments and our own additional analyses, we are
removing the requirement for flares to meet the long-term 60 ppmv
H2S fuel gas concentration limit. As explained in section
IV, we determined that requiring refineries to ensure the fuel gas they
send to their flares meets a long-term H2S concentration of
60 ppmv is not appropriate for flares.
We are promulgating final amendments for flares that include a
suite of standards that apply at all times that are aimed at reducing
SO2 emissions from flares. These amendments include several
provisions that were proposed on December 22,
[[Page 56430]]
2008, as well as others that differ from those proposed, but are a
logical outgrowth of the proposed amendments. This suite of standards
requires refineries to: (1) Develop and implement a flare management
plan; (2) conduct root cause analyses and take corrective action when
waste gas sent to the flare exceeds a flow rate of 500,000 standard
cubic feet (scf) above the baseline flow to a flare in any 24-hour
period (rather than the proposed threshold of 500,000 scf in any 24-
hour period without considering the baseline); (3) conduct root cause
analyses and take corrective action when the emissions from the flare
exceed 500 lb of SO2 in a 24-hour period (instead of 500 lb
SO2 above the emissions limit); and (4) optimize management
of the fuel gas by limiting the short-term concentration of
H2S to 162 ppmv during normal operating conditions
(determined hourly on a 3-hour rolling average basis). As explained
further in preamble section IV.B, 40 CFR part 60, subpart J sets a
performance standard for SO2 (expressed as a 162 ppmv short-
term H2S concentration limit) in fuel gas entering fuel gas
combustion devices. However, for this final rule, we have determined
that flares should be treated separately from other fuel gas combustion
devices because they meet the criteria set forth in CAA section
111(h)(2)(A) since emissions from a flare do not occur ``through a
conveyance designed and constructed to emit or capture such
pollutant.'' The flare itself is not a ``conveyance'' that is
''emitting'' or ``capturing'' these pollutants. Instead, pollutants
such as SO2 are created in the flame that burns outside the
flare tip. Therefore, we have determined that this suite of work
practice standards, which includes optimization of fuel gas management
(based on limiting concentration of H2S to 160 ppmv) is more
appropriate for flares, as opposed to the H2S performance
standard in subpart J, applicable to fuel gas systems. See section IV.B
of this preamble for a more detailed explanation of these requirements.
In this rule, we are using the term ``normal operating conditions'' to
describe situations where the process is operating in a routine,
predictable manner, such that the gases from the process are
predictable, as opposed to less-predictable swings related to emergency
situations during which the flare begins to operate as a safety device.
All of these requirements will apply during the vast majority of the
time. Under a very narrow and limited set of circumstances, such as
when a flare is used as a safety device under emergency conditions,\3\
the flare will be subject to all of these requirements except for the
requirement to optimize management of the fuel gas.
---------------------------------------------------------------------------
\3\ Background Information for New Source Performance Standards,
Vol. 3, Promulgated Standards (APTD-1352c; Publication No. EPA 450/
2-74-003), pg 127 (February 1974) (NSPS BID Vol. 3).
---------------------------------------------------------------------------
In addition, we are specifying that, if a discharge exceeding
either or both of the SO2 or flow thresholds described above
is the result of a planned startup or shutdown of a refinery process
unit or ancillary equipment connected to the flare, and the flare
management plan procedures for minimizing flow (which minimizes
emissions) during that type of event are followed, a root cause
analysis and corrective action analysis are not required. Finally, we
are finalizing the proposed added provisions to ensure that owners and
operators implement corrective actions on the findings of the
SO2 or flow rate root cause analyses and to specify a
deadline for performing the corrective actions.
We are finalizing the proposed amendment to remove the 250,000 scfd
30-day average flow rate limit. Our rationale for this decision is
explained in the preamble to the proposed amendments (73 FR 78530) and
also in section IV of this preamble.
We are finalizing one proposed amendment to the flare management
plan and adding several new requirements as a logical outgrowth of the
proposed amendments, considering the public comments we received, to
ensure compliance with the flare standards. First, as proposed, we are
requiring a list of refinery process units and fuel gas systems
connected to each affected flare. However, we are also adding a
requirement for a simple process flow diagram showing the design of the
flare, connections to the flare header and subheader system(s), and all
gas lines associated with the flare. With these two requirements, we
are clarifying that the flare management plan must include a diagram of
the flare and connections, but the diagram need not be a detailed
piping and instrumentation diagram that shows all process units and
ancillary equipment connected to the flare. We are also requiring the
owner and operator of an affected flare to assess and minimize flow to
affected flares from these process units and fuel gas systems. Second,
we are adding new requirements that the flare management plan include
design and operation details about the affected flare, including tip
diameter, type of flare, monitoring methods and a description of the
flare gas recovery system, if present. The inclusion of these details
will ensure that the rest of the flare management plan is reasonable
and appropriate for that affected flare.
Third, as a logical outgrowth of the proposed amendments,
considering the public comments we received, we are adding a new
requirement for owners and operators to determine the baseline flow to
each flare, including purge and sweep gas, and include this baseline
flow in the flare management plan. As described later in this preamble,
developing the baseline is important because the final threshold for
the flare flow root cause analysis takes this baseline flow into
consideration. Finally, we are adding a new requirement to minimize the
volume of gas flared during maintenance of a flare gas recovery system.
We have decided to remove the requirement for the owner or operator
to explain in the flare management plan how a root cause analysis and
corrective action analysis will be conducted if the flow to the flare
exceeds the specified threshold. Instead, all the requirements for
determining when and how to conduct a root cause analysis and
corrective action analysis, and the requirements for when and how to
implement a corrective action, have been expanded, as described later
in this section, and moved to 40 CFR 60.103a(c) through (e).
We are specifying that, for modified flares, the flare management
plan must be developed and implemented by no later than November 11,
2015 or upon startup of the modified flare, whichever is later (the
proposed amendments provided 18 months with an additional 6 months if
the owner or operator committed to installing a flare gas recovery
system). In addition, because of the lack of a direct flow limit and
the addition of the baseline flow value, we are adding a requirement
that the flare management plan must be submitted to the Administrator.
As with the flare management plan, the owner or operator of an
affected flare must comply with the root cause analysis and corrective
action analysis requirements within 3 years from the effective date of
this final rule or upon startup of the modified flare, whichever is
later.
We are finalizing several proposed amendments to the sulfur
monitoring requirements and revising other requirements as a logical
outgrowth of the proposed amendments, considering the public comments
we received. We consolidated the proposed alternatives to monitor
reduced sulfur compounds and total sulfur compounds into a
[[Page 56431]]
provision that allows the use of total reduced sulfur monitoring. We
also clarified the span requirements for these monitors and are
allowing the use of cylinder gas audits for relative accuracy
assessments. We are finalizing the H2S monitoring
alternative method for determining total sulfur content in the flare
gas, as proposed, but we have clarified the span requirements for this
monitor and are allowing the use of cylinder gas audits for relative
accuracy assessments, similar to the total reduced sulfur monitor
requirements. For refineries that measure SO2 concentrations
in the exhaust from a fuel gas combustion device that combusts gas
representative of the gas discharged to the flare, we added an
alternative to allow the owner or operator to use the existing
SO2 CEMS data to calculate the total sulfur content in the
flare gas.
We received public comments stating that the flow and sulfur
monitoring requirements for flares were too burdensome for flares that
are used infrequently or that are configured such that they cannot
receive high sulfur flare gas. Based on our evaluation of these
comments, we are providing new alternatives to continuous flow and
sulfur monitoring for certain flares. First, for flares that are
configured such that they only receive inherently low sulfur gas
streams described in 40 CFR 60.107a(a)(3)(i) through (iv) or (b),
continuous sulfur monitors are not necessary because a root cause
analysis will be triggered by an exceedance of the flow rate threshold
long before they exceed the 500 lb SO2 trigger in a 24-hour
period.
Second, we are providing an alternative monitoring option for
emergency flares, secondary flares and flares equipped with a flare gas
recovery system designed, sized and operated to capture all flows
(except flows resulting from planned startup and shutdown that are
addressed in the flare management plan). If this option is applicable,
the owner or operator may elect to continuously monitor the water seal
height and the pressure in the flare header just upstream of the water
seal rather than install total sulfur and flow monitoring systems. If
this monitoring option is selected, any instance where the pressure
upstream of the water seal (expressed in inches of water) exceeds the
water seal height triggers a requirement to perform a root cause
analysis and corrective action analysis, unless the discharge is
related to flare gas recovery system compressor cycling or a planned
startup or shutdown (of a refinery process unit or ancillary equipment
connected to the flare) following the procedures in the flare
management plan. An ``emergency flare'' is a flare that combusts gas
exclusively released as a result of malfunctions (and not startup,
shutdown, routine operations or any other cause) and is characterized
as having four or fewer discharge events in any 365 consecutive
calendar days.
Owners or operators of affected flares that have flare gas recovery
systems with staged compressors that elect to use this monitoring
option must identify these flares in their flare management plan,
identify the time period required for the staged compressors to
actively start to recover gas and identify the operating parameters
monitored and procedures employed to minimize the duration of flaring
during compressor staging. If a pressure exceedance is caused during
compressor staging and the duration of the pressure exceedance is less
than the time specified in the flare management plan, then a root cause
analysis is not required and the pressure exceedance is not required to
be reported. If a pressure exceedance is not attributable to compressor
staging (i.e., all staged compressors are active), if a pressure
exceedance is the result of a planned startup and shutdown event during
which the flare management plan is not followed or if the duration of a
pressure exceedance attributable to compressor staging is greater than
the time specified in the flare management plan, then a root cause
analysis and corrective action analysis are required and the pressure
exceedance must be reported. More than four pressure exceedances
required to be reported, as described above and under 40 CFR
60.108a(d)(5) (hereafter referred to as ``reportable pressure
exceedances'') in any 365 consecutive calendar days is an indication
that the flare gas recovery system is not adequately sized, and the
sulfur and flow monitors, as required in 40 CFR 60.107a(e) and (f),
must be installed if that occurs.
Third, we are clarifying that monitors for flow and sulfur on the
second flare in a staged flare configuration are not required where the
water seal monitoring requirements adequately and appropriately address
this scenario. Under most circumstances, the root cause analysis is
expected to be triggered, based on the flow to or emissions from the
primary flare. However, in cases where the capacity of the primary
flare is small (less than 500,000 scfd), this may not always be the
case. Additionally, we consider the water seal monitoring on the
secondary flare to be appropriate to ensure that gases are not released
to the secondary flare inadvertently. We clarify in this final rule
that if a root cause analysis is triggered for the primary flare,
releases to the secondary flare do not trigger an additional root cause
analysis (i.e., the releases may be treated as one event). However, if
flow is diverted to the secondary flare, then a root cause analysis is
required, even if a root cause analysis was not triggered for the
primary flare, based on flow rate or SO2 emissions. In
addition, if flow is diverted to the secondary flare five or more times
in a 365-day period, flow monitoring of the secondary flare is
required. We anticipate that the upstream sulfur monitor on the primary
flare can be used to determine the sulfur content of the gas diverted
to the secondary flare.
In response to comments, we are also finalizing a new amendment
providing an alternative compliance option in 40 CFR 60.103a(g) and 40
CFR 60.107a(h) for certain flares. Specifically, for refineries located
in the SCAQMD, an affected flare subject to 40 CFR part 60, subpart Ja
may elect to comply with SCAQMD Rule 1118 as an alternative to
complying with the requirements for flares in 40 CFR 60.103a(a) through
(e) and the associated monitoring provisions in 40 CFR 60.107a(e) and
(f). Similarly, for refineries located in the BAAQMD, an affected flare
subject to subpart Ja may elect to comply with both BAAQMD Regulation
12, Rule 11 and BAAQMD Regulation 12, Rule 12 as an alternative to
complying with the requirements for flares in 40 CFR 60.103a(a) through
(e) and the associated monitoring provisions in 40 CFR 60.107a(e) and
(f). We are also finalizing specific provisions within the standards
for owners or operators (and manufacturers of equipment) to submit a
request for a determination of equivalence for ``an alternative means
of emission limitation'' that will achieve a reduction in emissions at
least equivalent to the reduction in emissions achieved under any of
the final subpart Ja design, equipment, work practice or operational
requirements in accordance with CAA section 111(h).
For fuel gas combustion devices and sulfur recovery plants, we are
correcting and clarifying the threshold for a root cause analysis and
corrective action analysis. The proposed root cause analysis threshold
for both types of process units was 500 lb SO2 above the
emission limit, but the proposed amendments directed the owner or
operator to compare the SO2 emissions to ``the period of the
exceedance'' for fuel gas combustion devices and ``the entire 24-hour
period'' for sulfur recovery plants. That language meant that if one
12-hour average for a sulfur
[[Page 56432]]
recovery plant was above the emission limit, the owner or operator
would have compared those emissions to the emissions allowed over an
entire 24 hours to determine if root cause analysis was required.
However, although a 12-hour average above the emission limit clearly
means that more SO2 was emitted than allowed by that
emissions limit, it is possible that, since the time periods being
compared were not analogous, the ``allowed emissions'' over 24 hours
could be more than the actual emissions that made up the one 12-hour
average. Upon further consideration, we see no reason for the
requirements to be different for fuel gas combustion devices and sulfur
recovery plants. Therefore, we are finalizing an amendment that states
that the threshold for a root cause analysis and corrective action
analysis for both sulfur recovery plants and fuel gas combustion
devices is 500 lb above the emission limit during one or more
consecutive periods of excess emissions \4\ or any 24-hour period,
whichever is shorter. This clarifying amendment is needed to ensure
that the magnitude of the emissions limit exceedance is properly
compared to what would have been emitted if the emissions were
equivalent to the emissions limit based on the averaging time allowed
for that emissions limit.
---------------------------------------------------------------------------
\4\ As noted above, the proposed amendments used the term
``period of the exceedance'' for fuel gas combustion devices. That
term was intended to have the same meaning as a period of excess
emissions (or multiple consecutive periods of excess emissions), as
defined in 40 CFR 60.106a(b) or 40 CFR 60.107a(i)). Therefore, the
final amendments refer to ``one or more consecutive periods of
excess emissions'' rather than ``period of the exceedance.''
---------------------------------------------------------------------------
Finally, we are finalizing the amendments at 40 CFR 60.108a(c) and
(d) mostly as proposed to clarify recordkeeping and reporting when a
root cause analysis and corrective action analysis are required. These
clarifications were needed to more clearly delineate the differences in
the recordkeeping and reporting requirements for flares, fuel gas
combustion devices and sulfur recovery plants. The differences between
the proposed amendments and the final amendments are corrections to be
consistent with changes to the root cause analysis and corrective
action analysis requirements already described. We are also finalizing
40 CFR 60.108a(c), as proposed, to add recordkeeping requirements for
the proposed monitoring option that is based on periodic manual
sampling and analysis to determine the total sulfur-to-H2S
ratio.
D. What are the final amendments to the definitions in 40 CFR part 60,
subpart Ja?
We proposed amendments to a number of definitions in 40 CFR
60.101a. This section describes whether we are finalizing the
amendments as proposed, finalizing an amendment different than (but as
a logical outgrowth of) what was proposed or not finalizing the
proposed amendment.
We are finalizing amendments to the definitions of ``flexicoking
unit'' and ``fluid coking unit,'' as proposed.
We are finalizing a definition of ``delayed coking unit'' that is
different than the proposed amendments to clarify what pieces are
included in a delayed coking unit. The final June 2008 rule did not
explicitly describe the pieces of a delayed coking unit. We proposed to
amend the definition in December 2008 to specify that a delayed coking
unit ``consists of the coke drums and associated fractionator.'' In the
course of evaluating public comments on the proposed definition, we
looked more closely at the operation of delayed coking units and
determined that the fractionators, quench water system and coke cutting
equipment are integral to the operation of a delayed coking unit.
Therefore, we are revising the definition of ``delayed coking unit'' in
these final amendments to include ``the coke drums associated with a
single fractionator and the associated fractionator; the coke drum
cutting water and quench system, including the jet pump and coker
quench water tank; process piping and associated equipment such as
pumps, valves and connectors; and the coke drum blowdown recovery
compressor system.'' Finally, to avoid any potential retroactive
compliance issues that could arise for certain delayed coking units
because of the changes to the definition of ``delayed coking unit''
between the proposal and the final rule, we are moving the date for
determining applicability of NSPS subpart Ja for those newly
constructed, reconstructed and modified delayed coking units
specifically affected by this change from the date of the proposal to
the promulgation date of these final amendments. See CAA section
111(a)(2).
We are finalizing definitions of ``forced draft process heater,''
``natural draft process heater'' and ``co-fired process heater,'' which
will enable owners and operators to determine the appropriate
subcategory for each of their process heaters. Based on public
comments, the final amendments have been revised slightly from the
proposed definitions to clarify that induced draft systems are defined
as natural draft process heaters and balanced draft systems are defined
as forced draft process heaters. We are also revising the definition of
``co-fired process heater'' to clarify that this type of process heater
does not include gas burners that have emergency oil back-up burners.
We are finalizing the definition of ``air preheat,'' as proposed,
except that we are substituting the term ``sensible'' for ``latent'' to
describe the heat recovered from exhaust gases.
We are finalizing the definitions of ``flare gas recovery system''
and ``process upset gas,'' as proposed, and we are adding a new
definition of ``flare gas header system.'' We are finalizing a revision
to the definition of ``flare'' to refer to the ``flare gas header
system'' rather than repeat the components of the flare gas header
system within the definition of flare. In addition, we are clarifying
in the definition of ``flare'' that, in the case of an interconnected
flare gas header system (i.e., two or more flare tips share the same
flare gas header system or are otherwise connected such that they
receive flare gas from the same source), the ``flare'' includes each
combustion device serviced by the interconnected flare gas header
system and the interconnected flare gas header system.
We are finalizing definitions of ``corrective action,''
``corrective action analysis'' and ``root cause analysis'' with minor
changes from proposal to update section references and to expand upon
the types of factors that should be taken into consideration for root
cause and corrective action analyses. We are adding definitions of
``purge gas'' and ``sweep gas'' to clarify the requirements of the
flare minimization plan. We are also adding new definitions of
``emergency flare,'' ``cascaded flare system,'' ``non-emergency
flare,'' ``primary flare'' and ``secondary flare'' to clarify the types
of flares that are and are not allowed to use the water seal monitoring
alternative for flares.
We are finalizing the amendments to the definition of ``petroleum
refinery,'' as proposed. As we noted in the preamble to the proposed
amendments, facilities that only produce oil shale or tar sands-derived
crude oil for further processing using only solvent extraction and/or
distillation to recover diluent that is then sent to a petroleum
refinery are not themselves petroleum refineries. Facilities that
produce oil shale or tar sands-derived crude oil and then upgrade these
materials and produce refined products would be petroleum refineries.
Additionally, facilities that produce oil shale or tar sands-derived
[[Page 56433]]
crude oil using any cracking process would be considered petroleum
refineries.
We are not finalizing the proposed amendments to ``refinery process
unit'' to avoid possible conflicts and confusion caused by having
different definitions for ``refinery process unit'' in 40 CFR part 60,
subparts J and Ja, but we are adding a new definition of ``ancillary
equipment'' and using this term to clarify that the flare modification
provisions and standards apply to the types of units listed in the
proposed definition of ``refinery process unit.'' Specifically, we are
defining ancillary equipment as equipment used in conjunction with or
that serve a refinery process unit. Ancillary equipment includes, but
is not limited to, storage tanks, product loading operations,
wastewater treatment systems, steam- or electricity-producing units
(including coke gasification units), pressure relief valves, pumps,
sampling vents and continuous analyzer vents.
We are amending the definition of ``fuel gas,'' as proposed, to
clarify that process units that gasify petroleum coke at a petroleum
refinery are producing refinery fuel gases. We also proposed to amend
the definition to state that gas generated by process units that
calcine petroleum coke into anode grade coke is not fuel gas. Based on
public comment, we are amending the definition to state that gas
generated by coke calciners producing all premium grade coke (rather
than just anode grade coke, as proposed) is not fuel gas. Also upon
consideration of public comments, we are amending the definition of
``fuel gas'' to clarify which vapor streams we intended to exclude. The
proposed definition indicated that vapors collected and combusted to
comply with specific standards were not considered fuel gas. The final
amended definition clarifies that vapors that are collected and
combusted in a thermal oxidizer or flare installed to control emissions
from wastewater treatment units other than those processing sour water,
marine tank vessel loading operations and asphalt processing units are
not considered fuel gas, regardless of whether the action is required
by another standard.
Finally, we are finalizing several proposed amendments to the
definition of ``sulfur recovery plant'' to clarify the intent of the
definition. We are correcting the spelling of ``H2S.'' We
are also clarifying that multiple units recovering sulfur from a common
source of sour gas produced at a refinery are considered one sulfur
recovery plant. In addition, we are clarifying that loading facilities
downstream of the sulfur pits are not part of the sulfur recovery plant
(the proposed definition only specified secondary sulfur storage
vessels).
E. What are the final technical corrections to 40 CFR part 60, subpart
Ja?
See Table 4 of this preamble for miscellaneous technical
corrections that we are finalizing throughout 40 CFR part 60, subpart
Ja. As mentioned previously, some of these technical corrections are in
response to straightforward issues raised by Industry Petitioners in
their August 21, 2008, supplement to their original petition for
reconsideration (Docket Item No. EPA-HQ-OAR-2007-0011-0246). Other
technical corrections are needed to correct typographical errors and to
correct equation and paragraph designations.
Table 4--Technical Corrections to 40 CFR Part 60, Subpart Ja
------------------------------------------------------------------------
Technical correction and
Section reason
------------------------------------------------------------------------
60.102a(f)(1)(ii)............................ Replace ``300 ppm by
volume of reduced sulfur
compounds and 10 ppm by
volume of hydrogen
sulfide (HS2), each
calculated as ppm SO2 by
volume (dry basis) at
zero percent excess
air'' with ``300 ppmv of
reduced sulfur compounds
and 10 ppmv of H2S, each
calculated as ppmv SO2
(dry basis) at 0-percent
excess air'' for
consistency of units and
to correct a
typographical error.
60.104a(d)(4)(ii)............................ Redesignate Equation 3 as
Equation 5 to provide
for the addition of new
Equations 3 and 4.
60.104a(d)(4)(iii)........................... Redesignate Equation 4 as
Equation 6 to provide
for the addition of new
Equations 3 and 4.
60.104a(d)(4)(v)............................. Redesignate Equation 5 as
Equation 7 to provide
for the addition of new
Equations 3 and 4.
60.104a(d)(8)................................ Redesignate Equation 6 as
Equation 8 to provide
for the addition of new
Equations 3 and 4.
60.104a(f)(3)................................ Redesignate Equation 7 as
Equation 9 to provide
for the addition of new
Equations 3 and 4.
Replace ``hourly'' with
``3-hour'' in the
definition of the new
Equation 9 variable
``Opacity limit'' and
replace ``source test
runs'' with ``source
test'' in the definition
of the new Equation 9
variable ``Opacityst''
to clarify the
information required for
new Equation 9.
60.104a(h)(5)(iv)............................ Redesignate the reference
to Equation 6 as a
reference to Equation 8
to provide for the
addition of new
Equations 3 and 4.
60.105a(b)................................... Replace ``in Sec.
60.102a(b)(1) shall
comply with the
requirements in
paragraphs (b)(1)
through (3) of this
section'' with ``in Sec.
60.102a(b)(1) that
uses a control device
other than fabric filter
or cyclone shall comply
with the requirements in
paragraphs (b)(1) and
(2) of this section'' to
clarify applicability of
the requirements and
remove the reference to
a nonexistent paragraph.
60.105a(b)(1)................................ Replace ``according to
the requirements in
paragraph (b)(1)(i)
through (iii) of this
section'' with
``according to the
applicable requirements
in paragraphs (b)(1)(i)
through (v) of this
section'' to clarify and
correct paragraph
reference.
60.105a(b)(1)(ii)(A)......................... Replace ``alterative''
with ``alternative'' to
correct the use of an
incorrect word.
60.105a(i)(5)................................ Replace ``Except as
provided in paragraph
(i)(7) of this section,
all rolling 7-day
periods'' with ``All
rolling 7-day periods''
to remove the reference
to a nonexistent
paragraph.
60.107a(a)(2)(i)............................. Replace ``320 ppmv H2S''
with ``300 ppmv H2S'' to
make the span value for
a H2S monitor consistent
with the span value in
40 CFR part 60, subpart
J.
60.108a(d)(5)................................ Replace ``the information
described in paragraph
(e)(6) of this section''
with ``the information
described in paragraph
(c)(6) of this section''
to correct the reference
to a nonexistent
paragraph.
------------------------------------------------------------------------
IV. Summary of Significant Comments and Responses
As previously noted, we received a total of 22 comments addressing
the proposed amendments. These comments were received from refineries,
industry trade associations, consultants, state and local environmental
and public health agencies, environmental groups and members of the
public. Brief summaries of the major comments and our complete
responses to those comments are included in the following sections. A
summary of the remainder of the
[[Page 56434]]
comments received during the comment period and responses thereto, as
well as more detailed summaries of the comments addressed in this
preamble, can be found in Standards of Performance for Petroleum
Refineries: Background Information for Final Amendments--Summary of
Public Comments and Responses, which is included in the docket for the
final amendments (Docket ID No. EPA-OAR-HQ-2007-0011). The docket also
contains further details on all the analyses summarized in the
responses below.
In responding to the public comments, we re-evaluated the cost and
emission reduction impact estimates of some of the control options and
re-evaluated the related BSER determinations. In our BSER
determinations, we took all relevant factors into account consistent
with other agency decisions.
A. Process Heaters
Comment: Commenters stated that new forced draft process heaters
cannot meet the proposed emissions limit of 40 ppmv NOX, so
the EPA should revise the emissions limits for new forced draft process
heaters to be the same as the limit for modified and reconstructed
forced draft process heaters (60 ppmv NOX). One commenter
referenced a general technical document written by a process heater
burner manufacturer regarding a new forced draft process heater at
their refinery to support the assertion that new process heaters cannot
meet the proposed limit without selective catalytic reduction or other
add-on controls. Another commenter also requested higher emissions
limits for new forced draft process heaters with air preheat.
Response: The commenters provided only limited and theoretical data
to support their argument that new forced draft process heaters cannot
meet the 40 ppmv (or 0.040 lb/MMBtu) NOX emissions limit.
Specifically, the John Zink white paper cited by the commenter
(submitted as an attachment to Docket Item No. EPA-HQ-OAR-2007-0011-
0296) stated only that the 40 ppmv emissions limit could not be
``guaranteed'' for a new forced draft process heater, based on the
design conditions, which included air preheat. Actual NOX
performance data for that commenter's new forced draft process heaters
are not available, as those particular process heaters are not yet
operational. As such, the actual performance of these forced draft
process heaters is still in question. However, we acknowledge that we
only have data for one new forced draft process heater without air
preheat that is currently operating that could meet a 40 ppmv
NOX emissions limit on a 365-day average. We conducted
additional data evaluations to determine appropriate limits and
averaging times for all process heaters at normal operating conditions
while considering this and other public comments we received. As part
of the data analysis effort, we obtained a year's worth of hourly CEMS
data for the new forced draft process heater without air preheat
capable of meeting 40 ppmv on a 365-day average. As discussed later in
this section, our analysis of the additional data that we obtained
following the proposal supported revising all NOX emissions
limits to be on a 30-day average basis. The data indicate that the 30-
day averages for the new forced draft process heater without air
preheat capable of meeting 40 ppmv on a 365-day average exceeded 40
ppmv 15 percent of the time, but none of the 30-day averages exceeded
60 ppmv NOX.
Consequently, we are raising the NOX emissions limit
(while concurrently reducing the averaging time) for all new forced
draft process heaters to be equivalent to the emissions limit for
modified and reconstructed forced draft process heaters (i.e., 60 ppmv
or 0.060 lb/MMBtu with a 30-day averaging period). Furthermore, based
on the information provided by the commenters, as well as the available
performance data for existing forced draft process heaters with air
preheat that have been retrofitted with ultra-low NOX
burners, we also conclude that the 60 ppmv (or 0.060 lb/MMBtu) on a 30-
day rolling average basis adequately accommodates forced draft process
heaters that use air preheat. Based on our review of CEMS data for new
and retrofitted forced draft process heaters, we conclude that 60 ppmv
(or 0.060 lb/MMBtu) on a 30-day rolling average basis is BSER for new,
reconstructed or modified forced draft process heaters. (For additional
details, see Revised NOX Impact Estimates for Process Heaters, in
Docket ID No. EPA-HQ-OAR-2007-0011.)
Comment: Commenters asserted that the heating value-based emissions
limits (i.e., the limits in units of lb/MMBtu) should be numerically
equivalent to the concentration-based emissions limits (e.g., 40 ppmv
should be equivalent to 0.040 lb/MMBtu rather than 0.035 lb/MMBtu).
Response: In August 2008, Industry Petitioners provided the EPA
with suggestions for revising the process heater standards (Docket Item
No. EPA-HQ-OAR-2007-0011-0257). One of their recommendations was to
include emissions limits based on heating value (lb/MMBtu) to account
for hydrogen content variations in the fuel gas. They suggested that,
on an annual basis, most natural draft process heaters could meet 0.035
lb/MMBtu and all other process heaters could meet 0.055 lb/MMBtu. We
evaluated these suggested emissions limits and determined that they
were reasonably equivalent to the concentration-based limits we were
proposing. We also requested comment on their use and their
equivalency, as described in the preamble to the proposed amendments
(see 73 FR 78527). Industry commenters now assert that the emissions
limit numerically equivalent to the 40 ppmv concentration limit is
0.040 lb/MMBtu and the emissions limit numerically equivalent to the 60
ppmv concentration limit is 0.060 lb/MMBtu.
We note that, as discussed in the preamble to the proposed
amendments, the exact conversion from ppmv to lb/MMBtu depends on the
hydrogen content of the fuel gas. However, our calculations generally
support the more direct numerical conversion suggested by commenters
over the typical range of hydrogen concentrations expected in the fuel
gas (see Revised NOX Impact Estimates for Process Heaters, in Docket ID
No. EPA-HQ-OAR-2007-0011). Therefore, we are finalizing heating value-
based emissions limits of 0.040 lb/MMBtu and 0.060 lb/MMBtu for natural
draft process heaters and forced draft process heaters, respectively,
based on direct numerical conversions from the concentration-based
emissions limits.
We are also clarifying that the owner or operator must demonstrate
that the process heater is in compliance with either the applicable
concentration-based or heating value-based NOX limit. The
heating value-based NOX emission rate is calculated using
the oxygen (O2)-based F factor, which is the ratio of
combustion gas volume to heat input. Ongoing compliance with this
NOX emissions limit is determined using a NOX
CEMS and at least daily sampling of fuel gas heat content or
composition to calculate a daily average heating value-based emissions
rate, which is subsequently used to determine the 30-day average.
Specifically, if the F factor is determined at least daily, the
owner or operator may elect to calculate both a 30-day rolling average
NOX concentration (ppmv, dry basis, corrected to 0-percent
excess air) and a 30-day rolling average NOX emission factor
(in lb/MMBtu) and demonstrate that the process heater is in compliance
with either one of these limits. For most
[[Page 56435]]
fuel gas systems, the alternative emissions limits are expected to be
identical; however, there may be instances where a process heater may
be complying with one of the emissions limits and not the other. For
example, a process heater combusting fuel gas with very high hydrogen
content may have an average NOX concentration above the 60
ppmv limit, but below the 0.060 lb/MMBtu limit, largely due to the
concentration limit being determined on a dry basis (and understanding
that the combustion of hydrogen produces only water and not carbon
dioxide). Provided that the appropriate monitoring is conducted, an
affected source would only be out of compliance if it exceeds both the
concentration-based limit and the heating value-based limit at the same
time. However, to have the option to determine compliance with the
alternative heating value-based emissions limit, the refinery owner or
operator must, at least daily, determine the F factor (dry basis) for
the fuel gas according to the monitoring provisions in 40 CFR
60.107a(d). If the F factor is not determined at least daily, the
heating value-based alternative cannot be used. Generally, fuel gas
heating value is important to the overall operation of refinery boilers
and process heaters; as such, refiners maintain their fuel gas within
an operating range that they need to fire these sources, often by
mixing with natural gas, etc., so we anticipate that most, if not all,
refiners will already have this information available on a daily basis.
Comment: Several commenters addressed the need for the rule to
address turndown, which is a period of time when process heaters are
firing below capacity. Commenters stated that during these periods, the
NOX concentrations will likely be above the emissions
limits, but the mass of NOX emissions is no greater than
when the heater is operating at full capacity because the lower firing
rate results in a lower exhaust flow rate. Commenters noted that
turndown conditions could exist for extended periods, so special
provisions are needed for these conditions. Commenters requested a
mass-based emission rate (lb/MMBtu limit multiplied by the heater's
rated capacity) that would apply when the process heater is firing at
less than full capacity (some commenters suggested 50 percent of
capacity; one commenter suggested 70-percent capacity as a cutoff). One
commenter also noted that process heaters must often operate at higher
O2 levels during turndown and requested that the proposed
maximum O2 operating limit not apply when small furnaces
that are not required to install CEMS are firing at less than full
capacity.
Response: In our proposed amendments, we provided a longer
averaging time (365-day average) so that short periods of turn-down
would not significantly affect the overall performance of the unit.
However, according to the commenters, the longer averaging time does
not adequately address turndown conditions. Therefore, we re-evaluated
the available data, including our existing data and additional data
provided by the industry, to determine the appropriate emissions limits
during different types of operation, including turndown. The additional
data provided by Industry and our evaluation of those data are included
in the docket for the final amendments (Docket ID No. EPA-OAR-HQ-2007-
0011). Based on our analysis of the data (described in greater detail
in the next paragraph), we concluded that a 30-day averaging period is
appropriate for the NOX emission limits under most operating
scenarios.
Upon examination of all available CEMS data, we determined that,
for periods of normal operation (i.e., firing at 50 percent or more of
design capacity), the proposed NOX emissions limits of 40
and 60 ppmv were not achievable for all process heaters using a 24-hour
averaging period (the averaging period included in the final June 2008
rule). From the available data, short-term fluctuations in the
NOX concentrations of process heaters using ultra-low
NOX burners caused them to exceed a 24-hour average limit
somewhat frequently, but a 30-day average provided adequate time to
average out the short-term fluctuations. We note that a few of the
process heaters operated at relatively high excess O2
concentrations at normal conditions (i.e., at exhaust O2
concentrations of 6 percent or more). These units had periods of excess
emissions above the 30-day average emission limits, but we rejected the
performance of these process heaters as BSER because of the high
exhaust O2 concentrations for these units during normal
(i.e., non-turndown) firing rates. That is, these process heaters were
not being operated optimally for reducing NOX emissions.
Furthermore, when these process heaters were operated at the lower
range of exhaust concentrations for the unit (although generally higher
than what would be considered optimal excess O2
concentrations for reducing NOX emissions), the process
heater could meet the applicable 40 or 60 ppmv emissions limit on a 30-
day averaging period. Based on our review of CEMS data for process
heaters with ultra-low NOX burners that operated at excess
O2 concentrations less than 6 percent (i.e., operated in a
manner consistent with proper low NOX burner operation), all
such process heaters could comply with the final NOX
emissions limits on a 30-day average basis. Consequently, we revised
the basic emissions limits to be on a 30-day average.
As described previously in this section, we conclude that the
applicable 40 or 60 ppmv emissions limit on a 30-day averaging period
is achievable for process heaters during periods of normal operation.
Our next step was to evaluate the achievability of the emissions limits
during turndown conditions and alternative approaches for establishing
emissions limitations where necessary. The following paragraphs
describe our analysis of the data, including our evaluation of
alternative methods for accommodating turndown conditions and our
rationale for providing the site-specific alternative for extended
turndown conditions.
There were very limited CEMS data available for process heaters
operating under turndown conditions (i.e., firing below 50 percent of
design capacity). However, two general trends were observed in the CEMS
data that were available: (1) Typical exhaust O2
concentrations increase at lower firing rates; and (2) exhaust
NOX concentrations (corrected to 0-percent excess
O2) increase with increasing O2 concentration
(regardless of firing rates). These data, along with the need to
operate the process heater at higher O2 concentrations
during low firing rates to maintain flame stability, suggest that an
alternative NOX emissions limit could, in some instances, be
needed to address extended turndown conditions (turndown events lasting
a majority of the 30-day averaging time). As such, we considered
alternative compliance options to address turndown conditions.
One alternative compliance option considered to address turndown
was a mass-based NOX emissions limit that would be
equivalent to the mass of NOX emitted from a unit meeting
the 0.040 (or 0.060) lb/MMBtu limit while firing at 50 percent of
capacity, as suggested by commenters. However, for most units for which
CEMS data are available, the alternative mass-based emissions limit did
not improve the ability of the process heater to meet the emissions
limit. We note that most of the process heaters were able to meet the
applicable concentration-based emissions limit (40/60 ppmv) or the
heating value-based (0.040/0.060 lb/MMBtu) emissions limit
[[Page 56436]]
during turndown. Therefore, the issue appears to be limited to a few of
the process heaters that must operate at relatively high excess
O2 concentrations during turndown conditions. For these
units, the alternative mass-based emissions limit that we were
considering rarely, if ever, provided a means for these units to comply
with the performance standard.
We understand that technology providers recommend operating process
heaters that are turned down at higher excess O2
concentrations to improve flame stability and ensure safe operation of
the process heater; however, based on the information provided by the
technology providers, there is still an optimal excess O2
concentration at which flame stability is achieved while minimizing
NOX formation. That is, even when a process heater is
operating at less than 50-percent design capacity, excess O2
concentrations should still be controlled to minimize NOX
formation within the safe operating constraints to maintain flame
stability. We do not have specific data on process heaters that are
near, but below, the concentration emissions limits when firing above
50-percent capacity, but cannot meet the concentration limit when
firing below 50-percent capacity, so we have no data that show that
process heaters operating at less than 50-percent design capacity and
controlling excess O2 concentrations cannot meet the
emissions limits. However, we acknowledge that the correlations with
firing rates and O2 and/or NOX concentrations and
the need for higher O2 concentrations to maintain flame
stability generally support the commenter's argument that a few
marginally compliant process heaters will have difficulty meeting the
basic emissions limit when the unit is turned down. As such, we
acknowledge that there may be periods of turndown in which a process
heater is operating as recommended, but may be unable to meet the
concentration or heating value-based emissions limits in the final
rule, especially when the unit is operated at turndown for extended
periods (e.g., for 20 days or more compared to the 30-day averaging
time). As the need for an alternative limit appears to be limited to a
few process heaters and the optimal O2 concentration is
expected to vary, based on fuel gas composition, we determined that a
site-specific emissions limit was the best approach to account for
these extended turndown conditions. As such, the final rule provides
owners and operators that have a process heater operating in turndown
for an extended period of time the option of developing a site-specific
emissions limit that would apply to those operating conditions and
requesting approval from the Administrator to use that limit.
For process heaters between 40 and 100 MMBtu/hr capacity that do
not install a NOX CEMS, turndown is also expected to be an
issue with respect to achieving the O2 operating limit. As
described above, higher O2 concentrations are generally
needed to maintain flame stability at low firing rates. To address
potential turndown compliance issues with the O2 operating
limit, we have provided an allowance for process heater owners or
operators to develop an O2 operating curve to provide
different O2 operating limits based on the firing rate of
the process heater. If a single O2 operating limit is
established, it must be determined when the process heater is being
fired at 70 percent or more of capacity (i.e., far from turndown
conditions). For process heaters that routinely operate at less than 50
percent of design capacity and require additional O2 to
maintain flame stability, a separate O2 operating limit
should be established for turndown by conducting a second performance
test while the unit is operating at less than 50 percent of capacity.
Additional performance tests can be conducted to develop O2
operating limits for additional operating ranges.
Comment: Several commenters requested that the EPA revise the
emissions limits for co-fired process heaters or remove the limits for
co-fired process heaters from this rulemaking and address them at a
later date due to lack of sufficient data to set an achievable
emissions limit. One commenter provided a white paper to support higher
emissions limits. Commenters also asserted that the averaging time for
the weighted average emission rate should be extended to 365 days. One
commenter noted that the notation ``ENOx,hour'' in Equation
3 was confusing since the purpose of the equation was to determine the
daily emission rate.
Response: The final June 2008 rule included only one emissions
limit for all co-fired process heaters, and Industry Petitioners
asserted that differences in the configuration and operation of
different types of process heaters warranted different emissions
limits. The proposed amendments introduced two specific emissions
limits for co-fired process heaters, one based on vendor guarantees for
the burners and one based on an average NOX concentration
for a combination of fuel gas and fuel oil. We note that, for purposes
of this rule, a co-fired process heater is defined as a process heater
that employs burners that are designed to be supplied by both gaseous
and liquid fuels. In other words, co-fired process heaters are designed
to routinely fire both oil and gas in the same burner. These do not
include burners that are designed to burn gas, but have supplemental
oil firing capability that is not routinely used (i.e., emergency oil
back-up).
To respond to the comments requesting higher emissions limits for
co-fired process heaters, we reviewed the white paper provided by one
commenter (submitted as an attachment to Docket Item No. EPA-HQ-OAR-
2007-0011-0308), as well as additional burner emissions test data
provided by another commenter \5\ (conducted under well-controlled
conditions using best available ultra-low NOX burner
technologies at the manufacturer's testing facility). This information
indicates that, for co-fired natural draft process heaters, a daily
average emissions limit calculated based on a limit of 0.06 lb/MMBtu
for the gas portion of the firing and 0.35 lb/MMBtu for the oil portion
of the firing is achievable. Similarly, the information indicates that,
for co-fired forced draft process heaters, a daily average emissions
limit calculated based on a limit of 0.11 lb/MMBtu for the gas portion
of the firing and 0.40 lb/MMBtu for the oil portion of the firing is
achievable. As noted above, these values are based on burner
performance tests, which are considered a better source of information
than the vendor guarantees that were relied upon to develop the
proposed emissions limit. Therefore, we are revising the NOX
emissions limits for co-fired process heaters to those described above.
We note that we have revised the concentration-based NOX
emissions limits to be on a 30-day average basis (same as the limits
for gas-fired process heaters). We have also revised the nomenclature
of the daily average emissions limit in Equations 3 and 4 (proposed
Equation 3) to be clear that we intend the limit to be determined on a
daily basis rather than on an hourly basis.
---------------------------------------------------------------------------
\5\ The commenter providing this data asserted that it is CBI.
We will follow our CBI regulations in 40 CFR part 2 in handling this
data. The data has been placed in the docket, but is not publicly
available.
---------------------------------------------------------------------------
We also note that the burner performance tests were conducted in a
controlled environment at the burner manufacturer's full-scale
facilities. While it is incumbent on the owner or operator of an
affected process heater to control certain operating parameters, such
as excess O2 concentrations, to the
[[Page 56437]]
extent possible, we recognize that the performance limits in the final
amendments are based on limited data, none of which are direct test
data for a co-fired process heater operated at a petroleum refinery. We
conclude that the low-NOX burner technologies exist, are
demonstrated and are cost effective for co-fired process heaters and
they are, therefore, BSER for co-fired process heaters. However, as the
performance limits are based on limited operational data, we also
conclude that it is reasonable to provide an alternative, site-specific
limit in the event that factors outside the influence of the burner
design and operation (such as nitrogen content in the fuel oil)
suggests the emission limits in the final rule are inappropriate for a
specific application. Consequently, co-fired process heaters that
cannot meet the limits specified above, can request approval for a
site-specific emissions limit, as allowed above, for process heaters
that operate for extended periods under turndown.
B. Flares
Comment: Several commenters asserted that routine connections to a
flare should not be considered modifications of the flare because they
do not change the maximum physical capacity of the flare and do not
generally increase emissions. One commenter asserted that the 40 CFR
part 60, subpart A General Provisions in 40 CFR 60.14 can and should
apply to flares, so a special modification provision for flares in 40
CFR part 60, subpart Ja is unnecessary. Commenters noted that some
connections to the flare have the primary purpose of reducing
emissions, which has been excluded under 40 CFR 60.14(e)(5), a
paragraph that is not limited to pollutants ``to which the standard is
applicable.'' One commenter noted that a single project may remove some
connections and add others such that the net emissions could actually
be reduced. Another commenter asserted that an increase in flow should
not be considered a modification because flow is not a regulated
pollutant.
Instead, commenters asserted that the modification provision for a
flare should focus on physical and operational changes that increase
emissions from the flare. One commenter suggested that the EPA should
focus the flare modification provision on connections that provide a
primary/routine flow from a process unit to the flare. Other commenters
suggested that the flare modification provision should be focused on
VOC and SO2 emissions and should only include connections
that result in a net increase of those pollutants emitted ``during
normal operations'' and connections that cause an increase in the total
volume of gas containing VOC or sulfur compounds under standard
conditions that could reach the flare.
Response: The agency made a conscious decision to promulgate a
separate provision for a flare modification in 40 CFR part 60, subpart
Ja (see 40 CFR 60.14(f)) because flares are operated differently from
other refinery process units, making it difficult to apply the
modification provision in the General Provisions (40 CFR 60.14) to
them. The physical capacity of a flare is based on the amount of gas
potentially discharged to a flare as a result of emergency relief.
Refiners frequently make connections to existing flares that result in
emissions increases at the flares, but may never approach the physical
capacity of the flare system. Contrary to commenters' assertions, the
flare modification provision in 40 CFR 60.100a(c) does meet the
statutory definition of ``modification'' in CAA section 111(a)(4),
which is ``any physical change in, or change in the method of operation
of, a stationary source which increases the amount of any air pollutant
emitted by such source or which results in the emission of any air
pollutant not previously emitted.'' It is axiomatic that the
connections to the flare described in 40 CFR 60.100a(c) qualify as
physical or operational changes to the flare. Additionally, we
explained in the proposed rule how these connections also resulted in
emissions increases from the flare (see 73 FR 78529). Thus, these types
of new connections of refinery process units (including ancillary
equipment) and fuel gas systems to the flare qualify as a
``modification'' of the flare and trigger subpart Ja applicability for
the flare.
Those connections we identified that do not increase emissions from
the flare were specifically excluded from triggering 40 CFR part 60,
subpart Ja applicability under this same provision (see 40 CFR
60.100a(c)(1)). Specifically, we proposed on December 22, 2008, that
the following types of connections to a flare would not be considered a
modification of the flare: (1) Connections made to install monitoring
systems to the flares; (2) connections made to install a flare gas
recovery system; (3) connections made to replace or upgrade existing
pressure relief or safety valves, provided the new pressure relief or
safety valve has a set point opening pressure no lower and an internal
diameter no greater than the existing equipment being replaced or
upgraded; and (4) replacing piping or moving an existing connection
from a refinery process unit to a new location in the same flare,
provided the new pipe diameter is less than or equal to the diameter of
the pipe/connection being replaced/moved. While we agree that there may
be other connections to a flare that would not result in an emissions
increase from the flare (see response to the next comment for specific
details), we disagree with the commenters that the flare modification
provision should be further limited beyond what is already provided in
the provision.
We disagree with commenters that we must consider the ``net''
emissions from the process unit and the flare when determining whether
a flare is modified. The affected facility is the flare and does not
include the process units that are tied into the flare header system.
See Asarco v. EPA, 578 F.2d 319, 325 (D.C. Cir. 1978) (holding that
emission increases had to be determined based on emissions from the
affected facility). We also disagree that a modification determination
should be limited to emissions increases of VOC or SO2.
Flares are known to emit VOC, SO2, carbon monoxide (CO), PM
and NOX, as well as other air pollutants, all of which are
relevant when determining whether a flare has been modified. See CAA
section 111(a)(4). That is, we consider the standards for flares to be
emission standards for VOC, SO2, CO, PM and NOX.
See, generally, 73 FR 35838, 35842, 35854-35856 (June 24, 2008); 73 FR
78522, 78533 (December 22, 2008), as well as Table 4 of this preamble.
Using the flare to control VOC emissions at other refinery process
units will increase CO, PM and NOX emissions from the flare
and are, therefore, considered modifications of the flare, even if
there is a net reduction in VOC emissions at the refinery.
In evaluating whether a flare has been modified, we consider
increases in flow to the flare to be directly indicative of increased
emissions from the flare. While we agree that ``flow'' is not a
pollutant, we evaluated flow limits as a means to reduce
SO2, VOC, CO, NOX and other emissions from the
flare. The emissions from the flare are very difficult, if not
impossible, to measure accurately, but flow to the flare can be
measured, and the flow to the flare generates SO2, VOC, CO,
PM, NOX and other emissions. Therefore, a physical or
operational change to a flare that causes an increase of flow to the
flare will increase emissions of at least one of these pollutants and
is considered a modification of the flare.
Comment: Many commenters responded to the EPA's request for comment
on types of connections that
[[Page 56438]]
do not result in an increase in emissions from a flare. The commenters
suggested numerous specific connections that should not be considered
modifications, including:
(1) Connections made to upgrade or enhance (not just to install) a
flare gas recovery system;
(2) Connections made for flare gas sulfur removal;
(3) Connections made to install back-up equipment;
(4) Flare interconnects;
(5) All emergency pressure relief valve connections from existing
equipment;
(6) Connections of monitoring system purge gases and analyzer
exhausts or closed vent sampling systems;
(7) Purge and clearing vapors, block and bleeder vents and other
uncombusted vapors where the flare is the control device;
(8) Connections made to comply with other federal, state or local
rules where the flare is the control device;
(9) Connections of ``unregulated gases'' such as hydrogen,
nitrogen, ammonia, other non-hydrocarbon gases or natural gas or any
connection that is not fuel gas;
(10) New connections upstream of an existing flare gas recovery
system, provided the new connections do not compromise or exceed the
flare gas recovery system's capacity;
(11) Any new, moved or replaced piping or pressure relief valve
connections that do not result in a net increase in emissions from the
flare, regardless of piping or pressure relief valve size;
(12) Vapors from tanks used to store sweet or treated products;
(13) Temporary connections for purging existing equipment, as these
are essentially ``existing'' connections; and
(14) Connections of safety instrumentation systems (SIS) described
under Occupational Safety and Health Administration (OSHA) process
safety standards at 29 CFR 1910.119, the EPA's risk management program
at 49 CFR 68 and/or American National Standards Institute (ANSI)/
International Society of Automation (ISA)-84.00.01-2004.
Response: We carefully reviewed the commenters' suggested changes
to the flare modification provision to determine whether there are
additional connections that should not be considered modifications to
the flare. We agree that the first four connections in the commenters'
list should not be considered modifications of a flare. Projects to
upgrade or enhance components of a flare gas recovery system (e.g.,
addition of compressors or recycle lines) will improve the operation of
the flare gas recovery system, and connections to these additional
components will not result in increased emissions. Connections made for
removal of sulfur from flare gas (Item 2 above) will generally result
in a slight decrease in volumetric flow and a large decrease in
emissions of SO2. Connections made to install back-up or
redundant equipment (Item 3 above), such as a back-up compressor, will
result in fewer released emissions if there is a malfunction in the
main equipment.
The request to exclude flare interconnections (Item 4 above) is a
complicated issue because interconnecting two separate flares alters
what we consider to be the affected facility. The definition of
``flare'' specifically includes the flare gas header system as part of
the flare. Prior to interconnecting the flares, presumably each flare
header system is independent, and there would be two separate
``flares,'' each of which could potentially be an affected facility
subject to 40 CFR part 60, subpart Ja. However, because the flare
includes the flare header system, we consider that an interconnected
flare system is a single affected facility, and we have amended the
definition of ``flare'' for clarity. We agree that interconnections
between flares will not alter the cumulative amount of gas being flared
(i.e., interconnecting two flares does not result in an emissions
increase relative to the two single flares prior to interconnection).
We also see cases where the emissions from a single flare tip will
likely be reduced due to the flare interconnect. For example, when a
large release event occurs, this gas will now flow to both of the
interconnected flares rather than a single flare. The maximum emission
rate for the original single flare actually decreases, while the
combined emissions from both flares is the same quantity as prior to
the interconnection. Considering this, we agree that the
interconnection of two flares does not necessarily result in a
modification of the flare and we have specifically excluded flare
interconnections from the modification provisions.
However, we also clarify in this response that when a flare that is
subject to 40 CFR part 60, subpart Ja is interconnected with a flare
that is not subject to subpart Ja, then the resulting interconnected
flare is subject to subpart Ja. That is, the only case in which an
interconnection between two (or more) flares results in a combined,
interconnected flare that is not subject to subpart Ja is when none of
the original individual flares were subject to subpart Ja.
Additionally, we note that if a new connection is made to the
interconnected flare, then the flare (including each individual flare
tip within the interconnected flare header system) is modified and
becomes an affected facility subject to subpart Ja.
While we agree that connections that do not increase the emissions
from the flare should not trigger a modification, we disagree with the
commenter that their other suggested connections do not increase the
flare's emissions at the time gases are discharged via the new
connection. Each of the commenters' suggestions is discussed in the
following paragraphs.
We previously proposed an exemption for emergency pressure relief
valve connections from existing equipment (Item 5 above) if they
replace or upgrade existing equipment and do not increase the
instantaneous release rate to the flare (i.e., the new pressure relief
valve has a pressure set point and diameter no greater than the
equipment being replaced). As stated previously in this preamble, we
are finalizing that amendment, as proposed. However, new connections,
even if they are made to ``existing equipment,'' will result in an
increase in flow to the flare during periods of process upset that
cause the pressure relief valve to open.
Connections of monitoring system purge gases and analyzer exhausts
or closed vent sampling systems (Item 6 above) will increase the
emissions from the flare. Similarly, connections of purge and clearing
vapors and block and bleeder vents (Item 7 above), also trigger a
modification of the flare because the increase of gas flow to the flare
will increase the emissions from the flare.
We recognize that connections to a flare may be made to comply with
other federal, state or local rules where the flare is an emissions
control device (Item 8 above). In fact, nearly all flares could be
considered ``control devices.'' We agree that using a flare as an
emissions control device is preferable to venting the process unit to
the atmosphere. However, while using the flare as an emissions control
device does decrease emissions from the process unit being controlled,
the increase of gas flow to the flare will increase the emissions from
the flare. Therefore, a connection from a process unit to a flare for
use as an emissions control device results in a modification of that
flare.
Comments suggesting that connections of ``unregulated gases'' such
as hydrogen, nitrogen, ammonia, other non-hydrocarbon gases or natural
gas or connections that are not ``fuel gas,'' should not be considered
a
[[Page 56439]]
modification of the flare (Item 9 above) are in conflict with the
statutory definition of ``modification.'' Each of the streams mentioned
by the commenter, when directed to a flare, will increase emissions of
at least one pollutant (either PM, CO or NOX) from the flare
(all of which the standard is intended to reduce). That is, we
reiterate that we consider the standards for flares to be emission
standards for VOC, SO2, CO, PM and NOX. As such,
we do not agree that the types of gas streams suggested by the
commenters should be exempt from the modification determination.
New connections upstream of an existing flare gas recovery system
(Item 10 above) will increase the likelihood of an event that would
cause an exceedance of the flare gas recovery system's capacity (even
if the new connections ``do not exceed the flare gas recovery system's
capacity'' under normal conditions), and the amount of gases sent to
the flare would increase as a result of such an event, thereby
increasing the emissions from the flare.
We reiterate that we proposed an exemption for any moved or
replaced piping or pressure relief valve connections of the same size.
However, we disagree with the commenter's suggestion that any ``new,
moved, or replaced piping or pressure relief valve connections that do
not result in a net increase in emissions from the flare regardless of
piping or pressure relief valve size'' should be exempted (Item 11
above). The premise of the suggested amendment is that new or larger
connections somehow will not increase emissions from the flare. We have
discussed new connections previously, so we will concentrate on the
``regardless of piping or pressure relief valve size'' comment in this
paragraph. First, the size of the pressure relief valve or piping does
correlate to the discharge rate to the flare, with larger pressure
relief valves or larger diameter piping allowing higher discharge rates
to the flare at a given pressure. In fact, larger pressure relief
valves and larger diameter pipes are specifically designed to allow
higher flow rates to the flare. Second, higher flow rates will lead to
higher emission rates. For a pressure relief event that occurs for
several hours, the flow rate to the flare during the first hour of
relief using the larger pressure relief valve or larger diameter piping
will be larger than the flow rate experienced using the smaller
pressure relief valve or smaller diameter piping and will result in
higher emissions from the flare. Therefore, we reject the notion that
larger diameter pipes and larger pressure relief valves do not increase
the emissions rate from the flare during a release event. We are
finalizing the proposed exemptions for moved or replaced piping or
pressure relief valves with the size and design restrictions for the
new piping or pressure relief valves as proposed on December 22, 2008.
Commenters suggested that connections of vapors from tanks used to
store sweet or treated products (Item 12 above) should not be
modifications because those gas streams have less than 162 ppmv
H2S. We reiterate that SO2 is not the only
pollutant emitted from flares and that the additional flow of sweet
gases will increase the emissions of at least one pollutant from the
flare, so we are not exempting these types of connections to the flare
from the 40 CFR part 60, subpart Ja flare modification provision.
However, we have amended the sulfur monitoring requirements for flares
to exempt vapors from tanks used to store sweet or treated products
from the flare sulfur monitoring requirements. This monitoring
exemption is justified because it is not needed for the purposes of a
root cause analysis or other compliance purpose. For these sweet
vapors, the flow rate root cause analysis threshold will be exceeded
well before the SO2 root cause analysis threshold.
We carefully considered temporary connections for purging existing
equipment (Item 13 above), but we failed to see how these temporary
connections are essentially ``existing connections.'' According to the
commenters, ``maintenance gases have been routed in some form or other
to the flare for years, and the temporary tie-in to accomplish that is
not a change and is not an increase in emissions when viewed from a
before and after perspective.'' If the connections already exist, then
opening an existing valve to allow for this type of purging would not
trigger a flare modification. If the connection is being relocated and
the piping used is the same diameter as the pre-existing connection,
then this scenario is adequately covered by the proposed exclusion for
relocated connections. However, if a new connection is made
specifically to purge an existing piece of equipment, this purge gas
unequivocally represents additional gas flow sent to the flare that did
not exist and could not exist prior to the connection being made.
Again, we consider that the increase in gas flow to the flare will
result in an increase in emissions of at least one pollutant from the
flare. As such, no exemption is provided for new connections to
existing equipment, regardless if these connections are temporary or
permanent. We also find that these types of flows should be expressly
considered in the flare management plan and that flaring from these
``temporary'' connections should be minimized to the extent
practicable.
The impact of connections of SIS described under OSHA process
safety standards at 29 CFR 1910.119, the EPA's risk management program
at 49 CFR 68 and ANSI/ISA-84.00.01-2004 (Item 14 above) should be
evaluated on a case-by-case basis to determine whether these
connections result in a flare modification. We expect that, if these
connections are made for flare monitoring purposes, these connections
are already excluded in the exemption for flare monitoring systems. If
the ``SIS'' are process unit analyzers and the new connections are
being made to connect the analyzer exhaust to the flare, these
connections would be considered a modification, as previously
discussed. The commenter may also be referring to new connections for
additional pressure relief valves identified in the safety reviews
required by the cited rules, which we would consider to be a
modification of the flare.
Following all of the above review and analysis, we are finalizing
three of the connections, as proposed, adding three of the connections
requested by commenters and revising one of the proposed connections as
requested by commenters in 40 CFR 60.100a(c)(1). Thus, the following
seven types of connections are not considered a modification of the
flare:
(1) Connections made to install monitoring systems to the flare.
(2) Connections made to install a flare gas recovery system or
connections made to upgrade or enhance components of a flare gas
recovery system (e.g., addition of compressors or recycle lines).
(3) Connections made to replace or upgrade existing pressure relief
or safety valves, provided the new pressure relief or safety valve has
a set point opening pressure no lower and an internal diameter no
greater than the existing equipment being replaced or upgraded.
(4) Connections that interconnect two or more flares.
(5) Connections made for flare gas sulfur removal.
(6) Connections made to install back-up (redundant) equipment
associated with the flare (such as a back-up compressor) that does not
increase the capacity of the flare.
(7) Replacing piping or moving an existing connection from a
refinery process unit to a new location in the same flare, provided the
new pipe diameter is less than or equal to the
[[Page 56440]]
diameter of the pipe/connection being replaced/moved.
Comment: Several commenters suggested that de minimis emission
increases and net emission decreases resulting from new connections to
a flare made to control and combust fugitive emissions such as leaks
from compressor seals, valves or pumps, should not be considered
modifications of a flare. One commenter suggested allowing site-
specific exemptions for connections that do not increase emissions or
that result in a de minimis emissions increase. However, another
commenter objected to setting a de minimis emissions increase to
determine whether a change to a flare is a modification and stated that
allowing a de minimis approach would cause confusion over the
applicability of 40 CFR part 60, subpart Ja because flare emissions are
difficult to estimate.
Response: In the preamble to our proposed amendments, the EPA
specifically requested comment on using the de minimis exception in the
flare modification provision. 73 FR 78522, 78529. Industry Petitioners
had suggested some type of de minimis emissions increase should be
allowed without triggering 40 CFR part 60, subpart Ja applicability.
Id. The EPA acknowledged that these exceptions are ``permissible but
not required'' under the modification provision in the CAA. Id. The EPA
also stated: ``We request comments on a de minimis approach and on
specific changes that may occur to flares that will result in de
minimis increases in emissions. We also request comments on the type,
number, and amount of emissions that would be considered de minimis.''
Id.
Industry Petitioners continue to recommend that any emissions
increases resulting from ``routine connections'' to the flare system
``will be de minimis'' and should not trigger 40 CFR part 60, subpart
Ja applicability at the flare, but they have not provided the comments
or data requested in the proposal preamble that the EPA could consider
to evaluate the impacts of such an approach. Docket Item No. EPA-HQ-
OAR-2007-0011-0311 (second attachment), pg 20. Industry Petitioners
again suggest that the EPA exercise its authority and ``authorize
exceptions from otherwise clear statutory mandates'' by promulgating de
minimis exemptions for the flare modification provision. Id.; Alabama
Power Co. v. Costle, 636 F.2d 323, 360 (D.C. Cir. 1979). As explained
in Alabama Power, the de minimis exception allows agency flexibility in
interpreting a statute to prevent ``pointless expenditures of effort.''
Id. However, as Industry Petitioners recognize, nothing mandates that
the EPA use its de minimis authority in any given instance, and courts
especially recognize the significant deference due an agency's use of a
de minimis exception. Id. at 400; Shays v. Federal Election Com'n, 414
F.3d 76, 113 (D.C. Cir. 2005); Environmental Defense Fund, Inc. v. EPA,
82 F.3d 451, 466 (D.C. Cir. 1996); Ass'n of Admin. Law Judges v. Fed.
Labor Relations Auth., 397 F.3d 957, 961 (D.C. Cir. 2005).
In exercising that discretion, the EPA must consider the cautionary
advice it received from the Alabama Court regarding its use of the de
minimis exception: ``EPA must take into account in any action * * *
that this exemption authority is narrow in reach and tightly bounded by
the need to show that the situation is genuinely de minimis.'' Id. at
361. The Court also noted that exemptions from ``the clear commands of
a regulatory statute, though sometimes permitted, are not favored.''
Id. at 358. The EPA must exercise this authority cautiously, and only
in those circumstances that truly warrant its application.
The EPA has found no basis for promulgating a de minimis exception
to the flare modification provision. Despite its assertions, Industry
Petitioners have still provided no data to support a finding that the
emissions increases resulting from the alleged ``routine connections''
to a flare system are truly ``trivial or [of] no value.'' Docket Item
No. EPA-HQ-OAR-2007-0011-0311 (second attachment), pg 20. Without the
requested information showing that ``the situation is genuinely de
minimis,'' Alabama Power, 636 F.2d at 361 and, therefore, warrants this
kind of exception, we believe such an exemption would be inappropriate.
Additionally, Industry Petitioners' example that ``venting a new
small storage tank to a flare system * * * easily would cost a typical
refinery tens of millions of dollars'' since ``the entire flare
system'' (emphasis in original) would be subject to subpart Ja is
unavailing for its argument that the EPA should promulgate a de minimis
exception for the flare modification provision. Docket Item No. EPA-HQ-
OAR-2007-0011-0311 (second attachment), pg 21. As the District of
Columbia Circuit specifically states in Shays, authority for
promulgating a de minimis exception ``does not extend to a situation
where the regulatory function does provide benefits, in the sense of
furthering regulatory objectives, but the agency concludes the
acknowledged benefits are exceeded by the costs.'' Shays, 414 F.3d 76,
114 (emphasis added). By focusing solely on cost, Industry Petitioners
are effectively asking the agency to engage in the type of cost-benefit
analysis prohibited by the Shays Court. Such cost analyses are improper
in these types of decisions. Industry Petitioners generally focus their
discussion on VOC emissions and effectively admit that connecting the
small storage tank to the flare system increases emissions from the
flare (e.g., ``uncontrolled tank emissions would be essentially
eliminated by combustion in a flare'' (Docket Item No. EPA-HQ-OAR-2007-
0011-0311 (second attachment), pg 21, emphasis added)). Furthermore,
they disregard additional emissions of NOX and CO resulting
from the combustion of these gases at the flare. Industry Petitioners
also provide no data quantifying these emissions increases and,
therefore, cannot demonstrate that they are ``trivial or [of] no
value'' or, in other words, that the emissions increases are, in fact,
de minimis. As releases to the flare are often event driven, one can
envision situations where the release from even a small storage tank
could be significant. On the other hand, the EPA sees a substantial
environmental benefit in requiring controls that will reduce the
cumulative emissions from a flare that becomes subject to 40 CFR part
60, subpart Ja because of any of these alleged ``routine connections.''
Thus, given the nature of releases to the flare, we determined that a
de minimis exemption from the modification provisions for flares is
unworkable and unwarranted.
Comment: One commenter stated that exempting flares \6\ from the
H2S concentration limits during startup, shutdown and
malfunction (SSM) events is illegal because the CAA requires continuous
compliance with standards of performance promulgated under CAA section
111. See CAA sections 111(a)(1), 302(k). For support, the commenter
cited Sierra Club v. EPA, 551 F.3d 1019 (DC Cir. 2008), in which the
Court stated: ``When sections 112 and 302(k) are read together, then,
Congress has required that there must be continuous section 112-
compliant standards.'' The commenter noted that the Court found that
the exemption from compliance with CAA section 112 standards during SSM
events violates
[[Page 56441]]
the CAA because the general duty to minimize emissions during SSM
events is not a CAA section 112-compliant standard. The commenter
asserted that the CAA also requires that a section 111-compliant
standard that reflects BSER \7\ be in effect at all times for flares.
---------------------------------------------------------------------------
\6\ The comments submitted referenced ``fuel gas combustion
devices'' as the affected source when describing the exemption
during SSM events. However, the exemption only applies to flares.
See 40 CFR 60.103a(h). The discussion in this preamble is,
therefore, focused on flares as distinguished from other types of
fuel gas combustion devices that are required to comply at all times
with the H2S concentration limits in 40 CFR
60.102a(g)(1).
\7\ The commenter asserted, without providing support, that it
is not BSER to exempt flares from the H2S concentration
limits during startup and shutdown events. The commenter also stated
that the EPA, at a minimum, must demonstrate how the exemption from
the H2S concentration limits during SSM events does, in
fact, represent BSER, but the commenter stated that the EPA has
failed to make this demonstration.
---------------------------------------------------------------------------
The commenter further asserted that work practice standards for
flares are not CAA section 111-compliant standards because this is not
one of those ``limited instances'' in which CAA section 111(h)
authorizes such standards. The commenter stated that the EPA must show
that a standard of performance for flares is ``not feasible to
prescribe or enforce'' because ``(A) a pollutant * * * cannot be
emitted through a conveyance designed and constructed to emit or
capture such pollutant, or that any requirement for, or use of, such a
conveyance would be inconsistent with any federal, state or local law
or (B) the application of measurement methodology to a particular class
of sources is not practicable due to technological or economic
limitations.'' See CAA section 111(h)(2). The commenter stated that
neither of these exemptions appear to apply and the EPA cannot claim
that it is infeasible to promulgate a standard of performance for
flares,\8\ so the EPA cannot set a work practice standard for flares.
Thus, the commenter asserted that a CAA section 111-compliant standard
does not continuously apply to flares since both the exemption from the
H2S concentration limits during SSM events and the flare
work practice standards are not lawful under the CAA.
---------------------------------------------------------------------------
\8\ The commenter cited the EPA's rationale for proposing work
practice standards for flaring in which we state: ``It is not
feasible to prescribe or enforce a standard of performance for these
sources because either the pollution prevention measures eliminate
the emission source, so that there are no emissions to capture and
convey, or the emissions are so transient, and in some cases, occur
so randomly, that the application of a measurement methodology to
these sources is not technically and economically practical.'' 72 FR
27178, 27194-27195 (May 14, 2007). In response, the commenter
stated: ``[T]he plain language of the Act recognizes that standards
of performance leading to the `capture' of emissions are not
infeasible [citation omitted], and EPA has proposed to apply
measurement methodologies to flares in spite of the transience of
their emissions.''
---------------------------------------------------------------------------
Another commenter disagreed and provided several reasons why they
believe the EPA may lawfully exempt flares from the H2S
concentration limits during SSM events. First, the commenter noted that
40 CFR part 60, subpart Ja was promulgated as part of the mandatory
periodic review of 40 CFR part 60, subpart J required by CAA section
111(b)(1)(B). The commenter noted that subpart J exempts a flare from
the H2S concentration limits when combusting certain gases
generated during SSM events (see 40 CFR 60.104(a)(1), 60.101(e)) and
stated that the record contains ``ample evidence'' to support
maintaining that provision in subpart Ja. The commenter asserted that
including these same provisions in subpart Ja is ``an appropriate
exercise of EPA's authority to `not review' this aspect of the existing
standard in light of the efficacy of the existing standard.'' See CAA
section 111(b)(1)(B).
Second, the commenter noted that the Sierra Club decision was
largely grounded in the Court's determination that Congress amended CAA
section 112 out of concern ``about the slow pace of EPA's regulation of
HAPs,'' eliminating much of the EPA's discretion and requiring sources
to ``meet the strictest standards'' without variance ``based on
different time periods.'' The commenter further explained that the
Court pointed to CAA section 112(d)(1) regarding the EPA's authority to
``distinguish among classes, types, and sizes of sources'' when
promulgating CAA section 112 standards as further evidence for
constraining the EPA's ability to adopt different standards applicable
during SSM events. In contrast, the commenter asserted that ``Congress
has expressed no such concern about EPA's efforts to implement section
111'' despite revisions to CAA section 111 in 1977 and 1990. Therefore,
the commenter asserted, Congress has ``effectively ratified EPA's
longstanding approach to SSM under the NSPS program,'' which includes
the exemption for flares from the H2S concentration limits
during SSM events.
The commenter also asserted that, regardless of the above and
despite the similar nature of the provisions in CAA sections 111 and
112, the EPA has the discretion to implement them differently ``under
the markedly differently context of the NSPS program v. the MACT
program.'' See Environmental Defense v. Duke Energy Corp., 549 U.S.
561, 575-576 (2007). For example, the commenter asserted that the word
``continuous'' as used in the NSPS program could be interpreted and
applied differently, as acknowledged by the Court in National Lime
Ass'n v. EPA, 627 F.2d 416, 434 (DC Cir. 1980) (deferring to agency
regarding the effect of ``the perplexing implications of Congress' new
requirement of systems of continuous emission reduction'' on the
agency's longstanding ``regulations permitting flexibility to account
for startups, shutdowns, and malfunctions''). The commenter urged the
EPA to exercise this discretion and ``reassert the many practical,
technical and economic factors'' that justify promulgating separate
standards for SSM events in the NSPS program.
Third, the commenter asserted that requiring flares to meet the
H2S concentration limits during SSM events does not
represent BSER for this time period. According to the commenter,
``startup and shutdown gases are intermittent streams that cannot be
cost effectively treated for sulfur removal because of their infrequent
occurrence, their scattered points of generation and their
variability.'' Therefore, for all of the above reasons, the commenter
asserted that exempting a flare from the H2S concentration
limits when combusting certain gases generated during SSM events is
lawful under CAA section 111.
Alternatively, the commenter stated that if a standard must apply
during SSM events, the flare work practice standards are appropriate in
lieu of the H2S concentration limit.
Response: Regardless of whether or how the Sierra Club decision
under CAA section 112 applies to NSPS promulgated under CAA section
111, we are promulgating final amendments for flares that include a
suite of standards that apply at all times and are aimed at reducing
SO2 emissions from flares. As described previously, this
suite of standards requires refineries to: (1) Develop and implement a
flare management plan; (2) conduct root cause analysis and take
corrective action when waste gas sent to the flare exceeds a flow rate
of 500,000 scf above the baseline; (3) conduct root cause analysis and
take corrective action when SO2 emissions exceed 500 lb in a
24-hour period; and (4) optimize management of the fuel gas by limiting
the short-term concentration of H2S to 162 ppmv during
normal operating conditions. Additionally, refineries must install and
operate monitors for measuring sulfur and flow at the inlet of all of
their flares. Together, these requirements provide CAA section 111-
compliant standards that collectively cover all operating conditions of
the flare.
As the commenter notes, CAA section 111(h)(1) allows the EPA to
promulgate a design, equipment, work practice or operational standard
or ``combination thereof,'' when ``it is not feasible to prescribe or
enforce a standard of performance'' which reflects BSER for the
particular affected source. CAA section 111(h)(2) defines the phrase
[[Page 56442]]
``not feasible to prescribe or enforce a standard of performance'' as
``any situation in which the Administrator determines that * * * a
pollutant or pollutants cannot be emitted through a conveyance designed
and constructed to emit or capture such pollutant, or that any
requirement for, or use of, such a conveyance would be inconsistent
with any Federal, State, or local law, or * * * the application of
measurement methodology to a particular class of sources is not
practicable due to technological or economic limitations.''
We have determined that flares meet the criteria set forth in CAA
section 111(h)(2)(A) because emissions from a flare do not occur
``through a conveyance designed and constructed to emit or capture such
pollutant.'' Gases are conveyed to the flare for destruction, and
combustion products such as SO2 are not created until
combustion occurs, which happens in the flame that burns outside of the
flare tip. In other words, the SO2, NOX, PM, CO,
VOC and other pollutants generated from burning the gases are only
created once the gases pass through the flare and come into contact
with the flame burning on the outside of the flare. The flare itself is
not a ``conveyance'' that is ``emitting'' or ``capturing'' these
pollutants; instead, it is a structure designed to combust the gases in
the open air. Thus, setting a standard of performance for
SO2 (and other pollutants) is not ``feasible,'' allowing the
EPA to instead promulgate standards under CAA section 111(h), which
will collectively limit emissions from the flare.
The EPA previously promulgated a standard of performance for
SO2 emissions for fuel gas combustion devices which also
applied to flares. 39 FR 9308, 9315 (March 8, 1974). The standard is
expressed as an H2S concentration limit because it was
developed as an alternative to measuring the SO2
concentration in the stack gases exiting fuel gas combustion devices
other than flares (i.e., boilers and process heaters). That approach is
appropriate for fuel gas combustion devices other than flares because
measuring the H2S in the fuel gas combusted in those devices
is directly indicative of the SO2 emitted from the exhaust
stacks of those other devices. As explained in section III of this
preamble, we are, for the first time, designating flares as their own
affected facility. As such, in finalizing these amendments for flares,
we considered whether we could also apply a standard of performance for
SO2 emissions, expressed as an H2S concentration
limit or a total sulfur limit at the inlet to the flare. However, as
explained above, flares are substantially different from other fuel gas
combustion devices so that this approach is not workable for flares.
For example, SO2 emissions from a flare are dependent on
many factors, including the flow rates of all gases sent to the flare,
the total sulfur content of all gases sent to the flare and the
combustion efficiency at the flare. Each of these factors is also
dependent on many variables. For example, combustion efficiency at the
flare is dependent upon the flammability of the gases entering the
flare, the turbulence at the flare,\9\ the wind speed and wind
direction and the presence of other pollutants in the gases that can
react with the sulfur to form sulfur-containing pollutants other than
SO2. Since so many factors affect the potential formation of
SO2 emissions outside the flare tip, we realized that we
could not properly derive an H2S concentration limit or a
total sulfur limit at the flare inlet that would directly correlate
with those SO2 emissions. Thus, we determined that we cannot
set a standard of performance for SO2 emissions at the
flare.
---------------------------------------------------------------------------
\9\ Turbulence is needed to insure good mixing at the flare, but
is affected by whether the flare is assisted with air or steam or
non-assisted.
---------------------------------------------------------------------------
However, we still recognize that reducing the amount of sulfur that
is sent to a flare will reduce the SO2 emissions at the
flare. Even with the uncertainty described above, we understand the
importance of refineries managing the fuel gas sent to their flares in
a way that minimizes the sulfur content so as to ultimately minimize
the SO2 emissions. Rather than eliminate the H2S
concentration limit altogether, we are instead requiring under CAA
section 111(h) that refineries limit the short-term concentration of
H2S to 162 ppmv in the fuel gas sent to flares during normal
operating conditions. Refineries rely on various methods for optimizing
the management of fuel gas, including the use of amine treatment and
flare gas recovery systems. Amine treatment removes the H2S
from the flare gas that generates the pollutants before the gas is sent
to the flare. Flare gas recovery systems remove the flare gas
altogether and instead treat this gas in a fuel gas treatment system to
be used elsewhere as fuel gas in the refinery. Requiring refineries to
meet this concentration limit at the flare ensures that the fuel gas
has been adequately treated and managed such that it can be used as
fuel gas in the fuel gas system elsewhere in the refinery. We are not
requiring refineries to meet this limit during other periods of
operation because flare gas recovery systems that capture gases prior
to amine treatment can be quickly overwhelmed and fail to properly
function during high fuel gas flows. Thus, requiring that flares meet
this H2S concentration limit during periods when high fuel
gas flows would likely overwhelm these flare gas recovery systems would
not fully address the circumstances refineries face in managing these
high flow periods. Designing flare gas recovery systems to capture the
full range of gas flows to the flare would not only require the ability
to predict the full range of gas flows in the flare headers, but also
would require refiners to install recovery compressors in a staged
fashion such that all events causing high gas flows could be captured
and managed, neither of which are practical. Therefore, promulgating
flare requirements that include the H2S fuel gas
concentration limit during normal operating conditions, coupled with
requirements for refineries to develop and implement a flare management
plan and conduct root cause analyses and take corrective action when
waste gas sent to the flare exceeds a flow rate of 500,000 scf above
the baseline or 500 lb of SO2 in a 24-hour period,
recognizes these unique circumstances while still requiring the
refinery to take all reasonable measures for reducing or eliminating
the flow and sulfur content of gases being sent to the flares.
We are aware that numeric SO2 emission limits for flares
have been established under state law and in Federal Implementation
Plan (FIP) regulatory requirements. Those source-specific circumstances
differ markedly from this nationally applicable rulemaking,
necessitating different decisions in two very different circumstances.
For example, the EPA's SO2 FIP for the Billings/Laurel,
Montana area includes a SO2 emission limit of 150 lb of
SO2 per 3 hours for four sources that apply to the flares at
all times. See 40 CFR 52.1392(d)(2)(i), (e)(2)(i), (f)(2)(i) and
(g)(2)(i). These source-specific limits were appropriately based on
dispersion modeling in the Billings/Laurel area to determine what was
needed to meet national ambient air quality standards (NAAQS) for
SO2 in the Billings/Laurel area. In contrast, the nationally
applicable standards and requirements we are promulgating in this rule
must represent the BSER achievable for an entire industry sector
scattered across the entire country. This requires that we consider
costs and other non-air quality factors that affect all petroleum
refineries nationwide in making that decision and not just as applied
to a
[[Page 56443]]
particular group of sources in a particular location.
Additionally, those four sources subject to the Billings/Laurel FIP
demonstrate compliance with the 150 lb SO2/3-hour emission
limit by measuring the total sulfur concentration and volumetric flow
rate of the gas stream at the inlet to the flare. See 40 CFR
52.1392(d)(2)(ii), (e)(2)(ii), (f)(2)(ii), (g)(2)(ii) and (h). Since
the FIP must include emissions limits that insure attainment and
maintenance of the NAAQS in the Billings/Laurel area, it was
appropriate, in setting the standards for the Billings/Laurel FIP, to
conservatively assume that 100 percent of the sulfur in the gases
discharged to the flare is converted to SO2, and based on
this conversion, set the numeric limit as a value that is not to be
exceeded. However, that same assumption is not appropriate when setting
national standards for flares. Instead, we must consider the many
factors affecting the formation of SO2 at the flare tip and
how these factors affect how much of the sulfur in the gases sent into
the flare actually converts to SO2. Therefore, although
setting such source-specific limits was appropriate to satisfy what the
modeling showed was necessary to meet the SO2 NAAQS in the
Billings/Laurel area, a different analysis and standard is appropriate
for a national rulemaking.
Therefore, for the reasons discussed above, the EPA is finalizing
this collective set of CAA section 111(h)-compliant standards for
flares, based on our interpretation of CAA section 111(h) as it applies
to flares.
Comment: Numerous commenters asserted that the long-term 60 ppmv
H2S fuel gas concentration limit is not cost effective for
flares and, therefore, not BSER for flares. The commenters noted that
the EPA did not include costs for compressors, additional amine units
and sulfur recovery units, and one commenter stated that the EPA did
not consider the range of costs that are incurred by individual
refineries. Commenters also asserted that the EPA overstated emission
reductions by using 162 ppmv H2S as a baseline because many
refinery streams currently sent to the flare contain H2S
concentrations below 162 ppmv, so 162 ppmv H2S does not
reflect long-term performance. Commenters noted that the British
thermal units (Btu) content of flare gas is highly variable and
generally lower than that used by the EPA, so the EPA's analysis
overestimated the value of the recovered flare gas. One commenter noted
that the EPA should have considered consent decree requirements in the
baseline SO2 emissions estimates.
One commenter stated that the long-term 60 ppmv H2S fuel
gas concentration limit could preclude some refineries from processing
high-sulfur crude oils, thereby limiting refining production capacity.
Another commenter noted that many flares will receive both fuel gas and
process upset gas, so it would be impossible to determine if an
exceedance is caused by the regulated fuel gas or by the exempt gas.
The commenter recommended that the EPA apply the long-term 60 ppmv
H2S fuel gas concentration limit only to fuel gas combusted
in process heaters, boilers and similar fuel gas combustion devices,
and not to flares, or that the EPA allow Alternative Monitoring Plans
to demonstrate compliance with the emissions limits for non-exempt gas
streams upstream of the flare header.
Response: We acknowledge that, at proposal, we determined that a
long-term 60 ppmv H2S fuel gas concentration limit was cost
effective primarily for process heaters, boilers and other fuel gas
combustion devices that are fed by the refinery's fuel gas system.
Based on the typical configuration at a refinery, adding one new fuel
gas combustion device to the fuel gas system would essentially require
the owner or operator to limit the long-term concentration of
H2S in the entire fuel gas system to 60 ppmv, so emission
reductions would result from all fuel gas combustion devices tied to
that fuel gas system. Upon review of the BSER analysis conducted at
proposal for fuel gas combustion devices, we now realize that the
analysis is not applicable to flares (See Docket Item No. EPA-HQ-OAR-
2007-0011-0289).
Moreover, since we are regulating flares separately from other fuel
gas combustion devices in this final rule, we should separately
consider whether a long-term H2S concentration limit is
appropriate for fuel gas sent to flares.
In developing the suite of CAA section 111(h) standards for flares,
we considered whether refineries should be required to optimize
management of their fuel gas by limiting the long-term H2S
concentration to 60 ppmv in addition to the short-term H2S
concentration of 162 ppmv during normal operating conditions. We
determined that, for refineries to demonstrate that their fuel gas
complies with a long-term H2S concentration of 60 ppmv,
refineries would have to install a flare gas recovery system (which was
not needed for other fuel gas combustion devices) and then upgrade the
fuel gas desulfurization system. Alternatively, refineries would have
to treat the recovered fuel gas to limit the long-term concentration of
H2S to 60 ppmv with new amine treatment units on each flare.
While some of the costs provided by the commenters did not include
the value of the recovered gas and appeared, at times, to include
equipment not necessarily required by the regulation, we generally
agree with the commenters, based on our own cost estimates, that
optimizing management of the fuel gas system to limit the long-term
concentration of H2S to 60 ppmv is not cost effective for
flares (see Table 4 below). We note that the costs provided by the
commenters and the costs and emissions reductions in our analysis are
the incremental costs and emissions reductions of going from the short-
term 162 ppmv H2S concentration to a combined short-term 162
ppmv H2S concentration and long-term 60 ppmv H2S
concentration. While we are aware that some consent decrees require
refineries to limit the concentration of H2S in the fuel gas
to levels lower than the short-term 162 ppmv H2S
concentration, our baseline when evaluating the impacts of a national
standard (in this case, 40 CFR part 60, subpart Ja) is the national set
of requirements to which an affected flare would be subject in the
absence of subpart Ja (i.e., the short-term 162 ppmv H2S
concentration limit in 40 CFR part 60, subpart J).
Table 4--National Fifth Year Impacts of Meeting a Long-Term 60 ppmv H2S Concentration for Flares Subject to 40 CFR Part 60, Subpart Ja
--------------------------------------------------------------------------------------------------------------------------------------------------------
Emission Emission Emission
Capital cost Total annual reduction reduction reduction Cost
($1,000) cost ($1,000/ (tons SO2/yr) (tons NOX/yr) (tons VOC/yr) effectiveness
yr) \a\ \b\ \b\ \b\ ($/ton)
--------------------------------------------------------------------------------------------------------------------------------------------------------
New..................................................... 80,000 15,000 6 34 130 84,000
[[Page 56444]]
Modified/Reconstructed.................................. 860,000 160,000 53 310 1,200 100,000
--------------------------------------------------------------------------------------------------------------------------------------------------------
\a\ Because of the heat content of recovered gas, each scf of recovered gas is assumed to offset one scf of natural gas; a value of $5/10,000 scf of
natural gas was used to estimate recovery credit.
\b\ These emission reductions are based on flares already meeting the short-term 162 ppmv H2S fuel gas concentration limit in 40 CFR part 60, subpart J
(i.e., these are the incremental emission reductions achieved from a baseline of optimizing management of the fuel gas system to limit the short-term
H2S concentration in the fuel gas to 162 ppmv to the originally proposed combined short-term 162 ppmv H2S concentration and long-term 60 ppmv H2S
concentration in the fuel gas).
Comment: Several commenters addressed the EPA's request for comment
on ``the equivalency of the subpart Ja requirements as proposed to be
amended today and the SCAQMD Rule 1118'' and ``whether EPA could deem a
facility in compliance with subpart Ja as proposed to be amended today
if that facility was found to be in compliance with SCAQMD Rule 1118,
or other equivalent State or local rules'' (73 FR 78532, December 22,
2008). One commenter disagreed with the EPA's position, alleging that
``EPA's suggestion that it can waive compliance with the NSPS in this
manner is contrary to the Clean Air Act.'' The commenter stated that
the EPA's suggestion ``that existing state and local requirements
render the federal requirements irrelevant only confirms that EPA's
proposed flaring requirements do not reflect the best technological
system of continuous emission reduction.'' 42 U.S.C. 7411(h)(1)
(emphasis added). The commenter also stated that the CAA already
provides a mechanism for implementation of alternative work practice
standards in narrowly defined circumstances (42 U.S.C. 7411(h)(3)); an
owner or operator may demonstrate to the Administrator that an
alternative means of emissions limitation is equivalent to the federal
standard on a case-by-case basis. Therefore, the commenter asserted,
the CAA clearly states that ``EPA's authority to waive federal work
practice standards is case specific.'' Finally, the commenter stated
that the EPA did not explain how emissions reductions achieved through
compliance with SCAQMD Rule 1118 are equivalent to 40 CFR part 60,
subpart Ja. Further, the commenter asserted that the EPA neither
identified other state or local rules that could be considered
equivalent to subpart Ja, nor explained how the EPA would determine
that a specific state or local rule is equivalent to subpart Ja.
Therefore, the commenter asserted, it is impossible to fully assess the
merit of the EPA's idea and provide meaningful comments.
Another commenter stated that ``most stringent'' is not one of the
criteria that must be applied under the law to determine BSER.
Therefore, the commenter asserted, it is not appropriate to argue that
the EPA did not properly determine BSER simply because there exist
state or local rules that are more stringent than federal requirements.
The commenter also asserted that the EPA has full authority to
establish alternative regulatory standards that are determined to be as
stringent as or more stringent than BSER, and CAA section 111(h)(3)
generally applies after the EPA has completed a national rulemaking and
an owner or operator requests approval for a site-specific alternative
at a later date. The commenter asserted that it is logical that, if an
alternative method is identified during the rulemaking process, ``the
law would allow EPA to establish a site-specific alternative [in the
rule itself] (especially, as under [CAA section 111], where the
alternative would have to be determined through notice and comment
rulemaking).''
Other commenters recommended that refineries complying with SCAQMD
Rule 1118 be deemed in compliance with 40 CFR part 60, subparts J and
Ja. According to one commenter, SCAQMD Rule 1118 is ``in all respects
equivalent to or more stringent than the corresponding requirements''
of subparts J and Ja. Commenters also recommended that refineries
should be able to consider compliance with BAAQMD Regulation 12, Rule
11 and Regulation 12, Rule 12 as compliance with the appropriate
provisions of subpart Ja. One commenter provided a table comparing each
of the six proposed flare management plan requirements in 40 CFR
60.103a(a) to the SCAQMD and BAAQMD regulations. The table identified
sections of BAAQMD Regulation 12, Rule 11 and Regulation 12, Rule 12
that are equivalent to the six subpart Ja flare management plan
requirements. The commenter also noted that SCAQMD Rule 1118 is only
equivalent to five of the proposed requirements; it does not require an
owner or operator to identify procedures to reduce flaring in cases of
fuel gas imbalance (although another commenter noted that SCAQMD Rule
1118 requires minimization of all flaring, including fuel gas
imbalance). While most commenters focused on the equivalence of the
flare management plan requirements of the SCAQMD and BAAQMD rules and
the flare management plan requirements of subpart Ja, one commenter
requested that the periodic sampling of BAAQMD Regulation 12, Rule 11
be considered equivalent to the continuous sulfur monitoring
requirements of subpart Ja for emergency flares.
Response: First, we note that there seems to be some
misunderstanding regarding how a determination that SCAQMD Rule 1118 or
BAAQMD Regulation 12, Rule 11 and Regulation 12, Rule 12 are equivalent
to 40 CFR part 60, subpart Ja would actually be implemented in subpart
Ja. The EPA will not ``waive'' the obligation to comply with subpart Ja
if the source is complying with SCAQMD Rule 1118 or BAAQMD Regulation
12, Rule 11 and Regulation 12, Rule 12. In other words, the EPA will
not allow the owner or operator to ``choose'' to comply with SCAQMD
Rule 1118 or BAAQMD Regulation 12, Rule 11 and Regulation 12, Rule 12
instead of subpart Ja. Rather, the source must always demonstrate
compliance with subpart Ja. If SCAQMD Rule 1118 or BAAQMD Regulation
12, Rule 11 and Regulation 12, Rule 12 are determined to be equivalent
to subpart Ja, then these requirements would be provided as an
alternative within subpart Ja for the source to demonstrate that it is
meeting the requirements of subpart Ja.
To assess the comments, we reviewed SCAQMD Rule 1118, BAAQMD
Regulation 12, Rule 11, and BAAQMD Regulation 12, Rule 12 and compared
[[Page 56445]]
these rules to the 40 CFR part 60, subpart Ja requirements we are
finalizing here. We have included documentation of this review in
Docket ID No. EPA-HQ-OAR-2007-0011 that shows the sections of each of
those rules that we consider are equivalent to the subpart Ja
requirements. We determined that SCAQMD Rule 1118 and BAAQMD Regulation
12, Rule 11 and Regulation 12, Rule 12 will result in equivalent to or
greater than the emissions reductions resulting from the subpart Ja
flare management plan requirements. As a result of our analysis, we
have amended subpart Ja, as described in the following paragraphs.
We determined that SCAQMD Rule 1118 is equivalent to the flare
requirements and monitoring, recordkeeping and reporting provisions for
determining compliance with the flare requirements in 40 CFR part 60,
subpart Ja. We also determined that the combined provisions of BAAQMD
Regulation 12, Rule 11 and BAAQMD Regulation 12, Rule 12 are equivalent
to the flare requirements and monitoring, recordkeeping and reporting
provisions for determining compliance with the flare requirements in
subpart Ja. Therefore, we have added specific compliance options for
flares that are located in the SCAQMD and are in compliance with SCAQMD
Rule 1118, as well as for flares that are located in the BAAQMD and are
in compliance with both BAAQMD Regulation 12, Rule 11 and BAAQMD
Regulation 12, Rule 12. Flares that are in compliance with these
alternative compliance options are in compliance with the flare
standards in subpart Ja. Specifically, 40 CFR 60.103a(g) specifies that
flares that are located in the SCAQMD may elect to comply with SCAQMD
Rule 1118 and flares that are located in the BAAQMD may elect to comply
with both BAAQMD Regulation 12, Rule 11 and BAAQMD Regulation 12, Rule
12 to comply with the flare management plan requirements of 40 CFR
60.103a(a) and (b) and the root cause analysis and corrective action
analysis requirements of 40 CFR 60.103a(c) through (e). In addition, 40
CFR 60.107a(h) indicates that flares that are located in the SCAQMD may
elect to comply with the monitoring requirements of SCAQMD Rule 1118
and flares that are located in the BAAQMD may elect to comply with the
combined monitoring requirements of both BAAQMD Regulation 12, Rule 11
and BAAQMD Regulation 12, Rule 12 to comply with the monitoring
requirements of 40 CFR 60.107a(e) and (f). The owner or operator must
notify the Administrator, as specified in 40 CFR 60.103a(g), that the
flare is in compliance with SCAQMD Rule 1118 or both BAAQMD Regulation
12, Rule 11 and BAAQMD Regulation 12, Rule 12. The owner or operator
must also submit a copy of the existing flare management plan (if
applicable), as specified in 40 CFR 60.103a(g).
We note that, as pointed out by commenters, an owner or operator
maintains the ability under CAA section 111(h)(3) to submit a request
to establish, on a case-by-case basis, that ``an alternative means of
emission limitation will achieve a reduction in emissions * * * at
least equivalent to the reduction in emissions'' achieved under the
flare standards of 40 CFR part 60, subpart Ja. Pursuant to CAA section
111(h)(3), we also included specific provisions within 40 CFR 60.103a
for owners or operators to submit a request for ``an alternative means
of emission limitation'' that will achieve a reduction in emissions at
least equivalent to the reduction in emissions achieved under the final
standards in subpart Ja.
Comment: Commenters suggested that the requirement to minimize
discharges to the flare in 40 CFR 60.103a(a)(1) should specifically
address routine discharges, and the EPA should limit the minimization
requirements to actions that: (1) Are ``consistent with good
engineering practices'' and (2) consider costs and other health and
environmental impacts, as required by section 111 of the CAA.
Response: We agree that the language in proposed 40 CFR
60.103a(a)(1) appears to require an assessment of flare minimization
irrespective of cost or other relevant considerations, as contained in
CAA section 111, which was not our intent. We are clarifying, through
this response, that cost, safety and emissions reductions may be
considered when evaluating what actions should be taken to minimize
discharges to a flare, but we disagree that the flare minimization
assessment should be limited to ``routine discharges.'' We have revised
the flare management plan requirements in 40 CFR 60.103a(a) to more
fully describe the types of information that must be evaluated and
included in the plan.
As noted in the summary of this rule (section III.C of this
preamble), we are finalizing our proposed withdrawal of the 250,000
scfd 30-day rolling average flow limit for flares. This limitation does
not adequately account for site-specific factors regarding flare gas
Btu content, ability to offset natural gas purchase and other
considerations. We find that these factors need to be addressed in a
site-specific basis and are more appropriately addressed through the
flare management plan. In the absence of the specific flow limitation,
we have included additional requirements in the flare management plan
to prompt a thorough review of the flare system so that, as an example,
flare gas recovery systems are installed and used where these systems
are warranted. We have also revised the flare minimization requirements
to require the flare management plans to be submitted to the
Administrator (40 CFR 60.103a(b)).
As part of the development of the flare management plan, refinery
owners and operators can provide rationale and supporting evidence
regarding the flare reduction options considered, the costs of each
option, the quantity of flare gas that would be recovered or prevented
by the option, the Btu content of the flare gas and the ability or
inability of the reduction option to offset natural gas purchases. The
plan will also include the rationale for the selected reduction option,
including consideration of safety concerns. The owner or operator must
comply with the plan, as submitted to the Administrator. Major
revisions to the plan, such as the addition of an alternative baseline
(see next comment for further detail on baselines), must also be
submitted to the Administrator.
In summary, although we did not incorporate the commenter's
suggested language for limiting the scope of the minimization
requirements to actions that are ``consistent with good engineering
practices'' and that ``consider costs and other health and
environmental impacts,'' we acknowledge that these are valid
considerations in the selection of the minimization alternatives
available for a given affected flare. We find that the process of
developing and submitting the flare management plan will ensure that
these factors are considered consistent with CAA section 111 and that
the requirement to minimize discharges to the flare is implemented
consistently across all affected sources.
Comment: Commenters asserted that the flare flow root cause
analysis threshold of 500,000 scf in any 24-hour period is arbitrary
and cannot be fairly applied to all flares at all refineries. One
commenter cited an ultracracker flare that routinely cycles from 5
million to 25 million scfd as an example of a flare for which the
threshold of 500,000 scf in any 24-hour period would result in constant
and meaningless root cause analyses. The commenters suggested removing
the numerical threshold and limiting root cause analysis to upsets and
malfunctions as initially promulgated in June 2008 (because root cause
analysis is generally only effective
[[Page 56446]]
for reducing non-routine flows) or using a site- or flare-specific
threshold instead. Even if the numerical threshold is revised, the
commenters suggested that a number of streams be excluded from the
calculation of flow, such as hydrogen and nitrogen, purge and sweep
gas, natural gas added to increase the Btu content of the flare gas and
gases regulated by other rules to avoid performing multiple root cause
analyses for routine events. One commenter suggested that owners or
operators should be able to use one root cause analysis report for an
event that occurs routinely (as allowed in the consent decrees).
Response: We proposed the flare flow root cause analysis threshold
of 500,000 scf in any 24-hour period because we projected that flare
gas recovery would be a cost effective emission reduction technique for
flares with fuel gas flows that routinely exceed 500,000 scfd, although
we acknowledge that the threshold at which flare gas recovery becomes
cost effective is strongly (inversely) correlated to the average Btu
content of the flare gas (i.e., a relatively small reduction in the Btu
content of the gas makes the recovery system significantly less cost
effective). Although we did not specifically exclude sweep or purge gas
from the flow, we expected that the flow rates of sweep or purge gas
(i.e., gases needed to ensure the readiness of the flare and the safety
of the flare gas system) would be negligible when compared to the root
cause analysis threshold of 500,000 scf in any 24-hour period. In fact,
in our original analysis of the appropriate flow rate root cause
analysis threshold (Docket Item No. EPA-HQ-OAR-2007-0011-0246), we
essentially assumed that the sweep and purge gas flow rates were zero,
and we estimated costs and emissions reductions of the 500,000 scf in
any 24-hour period threshold, based on recovering that amount of gas or
eliminating recurring events of that size (rather than 500,000 scf
minus the sweep or purge gas flow).
However, while we do not believe that 5 million scfd \10\ is a
reasonable base flow for a flare, we do acknowledge that the size of
the flare, as well as the flare header system, will greatly impact the
required flow needed to maintain the readiness of the flare. Although
we can derive suitable flare flow thresholds for average conditions,
these thresholds are not necessarily reasonable when applied to all
flows, and we did not intend for on-going root cause analyses to be
conducted on account of sweep or purge gas.
---------------------------------------------------------------------------
\10\ Regarding commenter's cited ultracracker flare example, it
is difficult to believe that sweep gas alone accounts for 5 million
scfd of flare gas flow. Additionally, a compositional analysis of
the base flare gas from the normal flow, based on data provided from
a DIAL study of this refinery, suggests that the base flare gas is
of sufficient quality to recover. It also appears, based on the data
provided by the commenter, that the hydrogen stream recycle
compressor was off-line approximately half the year. For such huge
gas flows, considering the cost of purchasing or producing
additional hydrogen and the emissions associated with that process,
it is reasonable to expect that the facility would have a back-up
compressor if the primary compressor is unreliable.
---------------------------------------------------------------------------
Therefore, rather than specifying a one-size-fits-all threshold,
the final rule requires facilities to develop their own base flare flow
rates as part of their flare management plan. A flow-based root cause
analysis is triggered if flows measured by the flow monitor exceed
500,000 scf greater than the base flare flow rate in any 24-hour
period. Evaluating the flow rate threshold above a baseline better
reflects our original analysis of the impacts of flow-based root cause
analyses when the sweep or purge gas flow rates are not negligible. We
also note that 40 CFR 60.103a(d) allows a single root cause analysis to
be conducted for any single continuous discharge that causes the flare
to exceed either the root cause analysis threshold for SO2
or flow for two or more consecutive 24-hour periods.
The final rule does not limit root cause analyses to upsets and
malfunctions of refinery process units and ancillary equipment
connected to the flare, nor does it explicitly allow owners or
operators to use one root cause analysis report for an event that
occurs routinely. When we decided to eliminate the numerical limit on
flare flow rate, we specifically increased the scope of the flare flow
root cause analysis to cover more than just upsets and malfunctions. We
also decided not to explicitly allow owners or operators to use one
root cause analysis report for an event that occurs routinely as a
means to discourage routine flaring of recoverable gas. However, we
recognize that there may be recurring discharges to the flare that are
not recoverable for various reasons. Therefore, the final rule does
allow for several base cases, which could include recurring
maintenance; this provision will avoid multiple root cause analyses for
a recurring event. As described above, the flare management plan (as
well as significant revisions to the plan to include alternative
baselines) must be submitted to the Administrator. The Administrator or
delegated authority (e.g., the state) may review the plan, although
formal approval of the plan is not required. Not specifying a formal
approval process is intended to minimize the burden associated with
reviewing flare management plans. Rather, the rule specifies elements
of the plan that need to be addressed in order for the plan to be
considered adequate and provides an opportunity for a delegated
authority to find the plan not adequate if they choose to do so.
We expect that a final flare management plan in compliance with 40
CFR part 60, subpart Ja will possess the following characteristics: (1)
Completeness (all gas streams are considered, all required elements are
included and all appropriate flare reduction measures are evaluated);
(2) accuracy (the emission reductions and cost estimates for the
different options are accurate); and (3) reasonableness (the selection
of reduction options is correct and the baseline flow value is
reasonable). If the Administrator identifies deficiencies in the plan
(e.g., the plan does not contain all the required elements, alternative
flare reduction options were not evaluated or selected when reasonable,
the baseline or alternative baseline flow rates are considered
unreasonable), the Administrator will notify the owner or operator of
the apparent deficiencies. The owner or operator must either revise the
plan to address the deficiencies or provide additional information to
document the reasonableness of the plan.
Comment: Commenters requested alternative monitoring options or an
exemption from continuous flow monitoring for: (1) Flares designed to
handle less than 500,000 scfd of gas; (2) pilot gas; (3) flares with
flare gas recovery systems; (4) emergency flares; and (5) secondary
flares. The commenters asserted that flow meters are costly and
engineering calculations, which are currently used, are sufficient to
evaluate when the flow to a flare exceeds 500,000 scf in any 24-hour
period. One commenter stated that, for flares with flare gas recovery
systems, the pressure drop across the flare seal drum can be used to
calculate flow rate.
Response: In the final rule, flow monitoring is used to determine
whether a root cause analysis is required rather than to ensure
compliance with a specific flow limit. We have reviewed the commenters'
suggestions and agree that, in certain specific cases, monitoring is
not necessary and should not be required. However, as a general rule,
we believe flow monitors are needed, not only to provide a verifiable
measure of exceedances of the flow root cause analysis threshold, but
also exceedances of the root cause analysis threshold of 500 lb
SO2 in any 24-hour period. In addition, when we evaluated
local rules,
[[Page 56447]]
such as the initial BAAQMD rule for flare monitoring, we saw that the
measured flare flow rates were several times greater than previously
projected by the facilities.
Consequently, we find great value in the flow monitoring
requirements for flares. These monitoring requirements will greatly
improve the accuracy of emissions estimates from these flares. The
resulting improved accuracy of flare emissions estimates will also lead
to better decision-making as we conduct future reviews of rules
applicable to petroleum refineries. We did consider each of the
commenters' suggested exemptions in light of this fact; our specific
considerations follow.
We did not specifically consider that some flares would not be
capable of exceeding the flow root cause analysis threshold (i.e.,
designed to handle less than 500,000 scfd of gas). However, these small
flares could still exceed the root cause analysis threshold of 500 lb
SO2 in any 24-hour period. As such, we did not provide an
exemption from the monitoring requirements for these small flares.
We agree that the monitoring of pilot gas flow is not needed. In
the final rule, a root cause analysis is required if the gas flow to
the flare exceeds 500,000 scf above the baseline in any 24-hour period.
The flow of pilot gas is considered to be part of the baseline flow and
is assumed to be constant. As such, monitoring of pilot gas would not
be necessary to determine whether a flare has exceeded 500,000 scf
above the baseline in any 24-hour period. In practice, the actual
baseline flow set for the flare may or may not expressly include the
pilot gas flow rate. Generally, the configuration of the flare header
is such that the flare flow monitor would not measure pilot gas flow.
In this case, the baseline flow determined for the flare would not
expressly include the pilot gas flow rate. If the flare flow monitor is
configured in such a way that it does measure pilot gas, then pilot gas
would be considered part of the baseline conditions for that flare.
We agree with commenters that flares with flare gas recovery
systems do have unique conditions and these warrant alternative
monitoring options. Additionally, we recognize that the monitoring
requirements may be burdensome for flares that are truly ``emergency
only'' (i.e., flares that flare gas rarely, if at all, during a typical
year) or for secondary flares in a cascaded flare system. These flares
are expected to have a water seal that prevents flare use during normal
operations and ensures that the pressure upstream of the water seal
(expressed in inches of water) does not exceed the water seal height
during normal operations (hereafter referred to as ``properly maintain
a water seal''). We find that, for these select types of flares, water
seal monitoring as an alternative to the flow (and sulfur) monitoring
provisions is appropriate.
For flares with a flare gas recovery system and other emergency or
secondary flares that properly maintain a water seal, the final rule
states that an owner or operator may elect to monitor the pressure in
the gas header just before the water seal and monitor the water seal
liquid height to verify that the flare header pressure is less than the
water seal, which is an indication that no flow of gas occurs. If the
flare header pressure exceeds the water seal liquid level, a root cause
analysis is triggered unless the pressure exceedance is attributable to
staging of compressors. This alternative reduces the costs associated
with installing sulfur and flow monitoring systems for flares that
rarely receive fuel gas. Engineering calculations can be used to
estimate the emissions during the event, but not for determining
whether or not a root cause analysis is required.
To ensure that this option is only used for flares that are truly
emergency flares and not for flares that are used for routine
discharges, the final rule contains a limit on the number of pressure
exceedances requiring root cause analyses that can occur in one year.
Following the fifth reportable pressure exceedance in any consecutive
365 days, the owner or operator must comply with the sulfur and flow
monitoring requirements of 40 CFR 60.107a(e) and (f). Based on a review
of available flaring data, we expect that gas may be sent to an
emergency flare three to four times per year, on average. Consistent
with this information, we are providing in these final amendments that
an ``emergency flare'' may receive up to four releases to the flare in
any consecutive 365-day period to account for year-to-year variability.
However, a flare receiving more than four discharges in a consecutive
365-day period can no longer be considered an ``emergency flare'' and
must install the required sulfur and flow monitors.
Comment: Commenters requested an exemption from continuous sulfur
monitoring or alternative monitoring options for flares handling only
gases inherently low in sulfur content, emergency flares, flares with
properly designed flare gas recovery systems and secondary flares. For
flares handling gases low in sulfur, the commenters noted that
continuous monitoring is unnecessary and certain fuel gas streams are
already exempted from monitoring if they are combusted in a fuel gas
combustion device. For flares that handle only gases exempt from the
H2S concentration requirements and flares with properly
designed flare gas recovery systems, commenters stated that engineering
calculations are sufficient to determine if the SO2 root
cause analysis threshold of 500 lb in any 24-hour period is exceeded.
One commenter requested that the EPA allow owners or operators to
submit and use an alternative monitoring plan to demonstrate that the
flare gas recovery system is operating within its capacity and to
calculate SO2 emissions from engineering calculations and
flare gas sampling. For secondary flares, one commenter noted that the
continuous sulfur monitor on the primary flare could be used to
determine the sulfur content of the gas being flared from the secondary
flare.
One commenter requested that the EPA allow the use of engineering
calculations to determine the sulfur-to-H2S ratio because
sampling can be difficult for emergency flares. One commenter noted
that the EPA should allow the use of an existing continuous monitoring
system if the gas sent to the flare is already monitored elsewhere. As
examples, the commenter cited fuel gas and pilot gas already monitored
within the fuel gas system.
For flares that rarely see flow, commenters particularly cited
difficulties with performance tests. Commenters noted that, to meet the
sulfur monitor performance test requirements, an owner or operator may
have to intentionally flare gas that may not meet the H2S
concentration limits. One commenter also stated that performing the
required relative accuracy test audit (RATA) could cause the flare to
exceed the root cause analysis threshold. The commenter recommended
revising the performance test requirements for flares with flare gas
recovery to require only a cylinder gas audit.
Response: We have amended the final rule so that gases that are
exempt from H2S monitoring due to low sulfur content are
also exempt from sulfur monitoring requirements for flares. For low-
sulfur gases, the flare root cause analysis will always be triggered by
an exceedance of the flow rate threshold well before the SO2
threshold is exceeded, so no sulfur monitoring is required. However,
this exemption can only be used for flares that are configured to
receive only fuel gas streams that are inherently low in sulfur
content, as described in 40 CFR
[[Page 56448]]
60.107a(a)(3), such as flares used for pressure relief of propane or
butane product spheres (fuel gas streams meeting commercial grade
product specifications for sulfur content of 30 ppmv or less) or flares
used to combust fuel gas streams produced in process units that are
intolerant to sulfur contamination (e.g., hydrogen plant, catalytic
reforming unit, isomerization unit or hydrogen fluoride alkylation
unit). We already clarified that flare pilot gas is not required to be
monitored. Also, 40 CFR part 60, subpart Ja already allows for
H2S monitoring at a central location, such as the fuel mix
drum, for all fuel gas combustion devices (and we are finalizing
amendments to ensure it is clear that H2S monitoring at a
central location is allowed for flares as well). Thus, we agree that if
a flare only burns natural gas, fuel gas monitored elsewhere or fuel
gas streams that are inherently low in sulfur content (as defined in 40
CFR 60.107a(a)(3)), then no H2S monitor is needed.
The remaining issue is whether or not sulfur monitoring is
necessary for ``emergency only'' flares. (An emergency flare is defined
as a flare that combusts gas exclusively released as a result of
malfunctions (and not startup, shutdown, routine operations or any
other cause) on four or fewer occasions in a rolling 365-day period.
For purposes of the rule, a flare cannot be categorized as an emergency
flare unless it maintains a water seal.) We acknowledge that there are
difficulties and costs with installing monitors on flares that rarely
operate. However, we are concerned about how the owner or operator will
detect emissions above 500 lb SO2 in any 24-hour period
during an upset or malfunction of a refinery process unit or ancillary
equipment connected to the flare. Commenters appear to have conflicting
opinions regarding the ability to sample the flare gas to determine the
sulfur content (or total sulfur-to-H2S ratio) during a
flaring event. If samples could be taken during the flaring events,
then that would be a potential option. However, during a process upset
or malfunction, focus should be on alleviating the problem rather than
taking a special sample. Also, given the duration of some of these
events, it appears unlikely that representative samples can be manually
collected.
Taking the difficulties discussed above into account, we have
developed an alternative monitoring option for emergency flares. As
noted in the previous response, emergency flares are expected to
properly maintain a water seal. We provide pressure and water seal
liquid level monitoring, as previously described as an alternative to
the sulfur and flow monitors. As described in more detail above, any
fuel gas pressure exceeding the water seal liquid level triggers a root
cause analysis and there is a limit to the number of exceedances in one
year. Under this option, a root cause analysis is triggered, based on
the monitored pressure and water seal height, so accurate measurements
of flow rate and sulfur concentrations are less critical than for
flares that must evaluate these parameters to determine if a root cause
analysis is needed. Consequently, for these flares, engineering
calculations can be used to estimate the reported emissions during the
flaring event, but the root cause analysis must be performed regardless
of the magnitude of these engineering estimates. Using this alternative
monitoring option, emergency flares are not required to install
continuous sulfur monitoring systems. Flares that do not meet the
conditions of an emergency flare are required to install continuous
sulfur monitoring systems and cannot elect this alternative monitoring
option.
We also agree that flaring solely for the purpose of a RATA or
other performance test is not desirable. The ``cylinder gas audit''
procedures requested by the commenter are described as alternative
relative accuracy procedures in section 16.0 of Performance
Specification 2 (referenced from Performance Specification 5). We
reviewed the alternative relative accuracy procedures and considered
how they may apply to flares, and we have determined that the
alternative relative accuracy procedures are appropriate for flares. We
expect that, for most affected flares, the variability in flow
(including no flow conditions) and sulfur content of the gases
discharged to the flare create significant barriers to the normally
required relative accuracy assessments, particularly if those
assessments need to be made over a range of sulfur concentrations
potentially seen by the monitor. Therefore, we are amending 40 CFR
60.107a(e)(1)(ii) and 40 CFR 60.107a(e)(2)(ii) to specify that the
owner or operator of a flare may elect to use the alternative relative
accuracy procedures in section 16.0 of Performance Specification 2 of
Appendix B to part 60. As required by 40 CFR 60.108a(b), the owner or
operator shall notify the Administrator of their intent to use the
alternative relative accuracy procedures.
Comment: One commenter requested that the EPA clarify whether the
additionally proposed sulfur monitoring options for flares are for
total reduced sulfur or total sulfur. The commenter noted that
measuring total sulfur is the simplest and most inclusive measurement
of SO2 emissions and it is the method included in SCAQMD
Rule 1118. The commenter also requested that methods for measuring
total sulfur in gaseous fuels be included as acceptable options to
perform the relative accuracy evaluations of the CEMS.
One commenter requested that provisions be made in 40 CFR
60.107a(e)(2) to develop a total sulfur-to-H2S (or total
reduced sulfur-to-H2S) ratio so that the total sulfur
monitor can be used for both the root cause analysis requirements and
for compliance with the requirement to limit short-term H2S
concentration in fuel gas sent to a flare to 162 ppmv without the need
for a duplicative continuous H2S monitor. Another commenter
supported the addition of alternative monitoring methods for the sulfur
content of flare gas, but noted that since the composition of flare gas
is highly variable, the alternative methods must meet continuous
monitoring requirements.
Response: We have clarified and consolidated the monitoring
requirements to allow total reduced sulfur monitoring for flares. For
the purposes of evaluating the SO2 root cause analysis
threshold, total sulfur monitoring provides the most accurate
assessment. However, in most cases, the vast majority of sulfur
contained in gases discharged to the flare is expected to be in the
form of total reduced sulfur compounds, which include carbon disulfide,
carbonyl sulfide and H2S. Our test method for measuring
total reduced sulfur includes the use of EPA Method 15A as a reference
method, and because EPA Method 15A measures total sulfur, the total
reduced sulfur monitoring requirement is equivalent to a total sulfur
monitoring method.
As discussed previously, we are relying on the suite of flare
requirements we are promulgating to limit SO2 emissions at
the flare. These include optimizing management of the fuel gas by
limiting the short-term concentration of H2S to 162 ppmv
during normal operating conditions. We expected most refineries would
already have the H2S monitor and did not consider the use of
a total sulfur monitor for use in complying with the short-term 162
ppmv H2S concentration in the fuel gas. As the
H2S concentration will always be less than the total reduced
sulfur concentration, it is acceptable to use the total reduced sulfur
monitor to verify that the fuel gas
[[Page 56449]]
does not exceed the short-term H2S concentration of 162
ppmv. Therefore, we have provided for the use of total reduced sulfur
monitors, provided the monitor can also meet the 300 ppmv span
requirement.
However, we have not provided a correction factor to scale down the
total reduced sulfur concentration to H2S. The owner or
operator using this method must essentially be able to demonstrate they
can achieve a 162 ppmv total reduced sulfur concentration in the fuel
gas. The concentration ratio was provided for the purposes of the root
cause analysis because of the costs of adding a total sulfur monitoring
system when a dual range H2S monitor was already in-place,
as well as the expected accuracy needed for the system to assess the
SO2 root cause analysis threshold. As few cases would exist
where the flaring event would be right at the SO2 root cause
analysis threshold of 500 lb in any 24-hour period, inaccuracies
associated with the average total sulfur-to-H2S ratio were
not expected to be significant.
On the other hand, the short-term 162 ppmv H2S
concentration in the fuel gas must be continuously maintained, and the
total sulfur-to-H2S ratio at these low concentrations is
expected to be highly variable, depending on the efficiency of the
amine scrubber systems. As the amine scrubber systems, according to
previous industry comments, are not effective for reduced sulfur
compounds other than H2S, the non-H2S reduced
sulfur concentration is expected to be fairly constant, with most of
the fluctuations in total sulfur content being attributable to
fluctuations in H2S concentrations. Consequently, we have
determined that the inaccuracies of the ratio approach are not
acceptable for continuously demonstrating that the short-term
concentration in the fuel gas does not exceed 162 ppmv H2S.
Therefore, owners or operators of affected flares may use the direct
output of a total reduced sulfur monitor to assess compliance with the
short-term 162 ppmv H2S concentration in the fuel gas, or
they must install a continuous H2S monitor.
Comment: One commenter supported the proposed amendment revising
the span value for fuel gas H2S analyzers to match the span
requirements in 40 CFR part 60, subpart J, stating this will save time
and money. However, the commenter stated that the span value for the
flare H2S monitoring option is too restrictive and suggested
that requirements in Appendix F to part 60 provide sufficient quality
assurance/quality control (QA/QC) without the need for the rule to
specify the span range. The commenter also requested clarification of
the sulfur monitor span for flares, suggesting that it should be based
on the H2S concentration limits and that engineering
calculations can be used to assess exceedances of the SO2
root cause analysis threshold of 500 lb in any 24-hour period.
Response: The H2S span value is at 300 ppmv to verify
compliance with the H2S concentration requirement for the
fuel gas; the span of the total sulfur monitor needs to be much greater
than that to be able to quantify the sulfur content in streams
containing several percent sulfur. For units that use the
H2S analyzers both to assess compliance with the short-term
162 ppmv H2S concentration requirement for the fuel gas and
to assess exceedances of the SO2 root cause analysis
threshold of 500 lb in any 24-hour period, a dual range monitor will be
necessary. For the purposes of the SO2 root cause analysis
threshold of 500 lb in any 24-hour period, we intended that the monitor
be capable of accurately determining the sulfur concentration for the
range of concentrations expected to be seen at the flare. We are
particularly interested in quantifying the concentrations of high
sulfur-containing streams as these would be the streams most likely to
trigger a root-cause analysis at low flows. We proposed that the span
for the flare sulfur monitor be selected from a range of 1 to 5
percent. We agree with the commenter that this may be too restrictive,
and we have revised the span requirements to be determined, based on
the maximum sulfur content of gas that can be discharged to the flare
(e.g., roughly 1.1 to 1.3 times the maximum anticipated sulfur
concentration), but no less than 5,000 ppmv. A single dual range
monitor may be used to comply with the short-term 162 ppmv
H2S concentration requirement for the fuel gas and the
SO2 root cause analysis threshold monitoring requirement
provided the applicable span specifications are met. In reviewing the
span specifications, we noted that span requirements were inadvertently
omitted from the total reduced sulfur compound monitoring alternative.
The purpose of these monitors is identical to the H2S
monitoring alternative, and the same span considerations apply for
these monitors.
We disagree that the QA/QC procedures in Appendix F to part 60 are
sufficient without specifying the span values. Procedure 1 of Appendix
F to part 60 defines ``span value'' as: ``The upper limit of a gas
concentration measurement range that is specified for affected source
categories in the applicable subpart of the regulation.'' The
concentrations used for calibration are based on the span value.
Several of the QA/QC procedures in Appendix F are undefined if the span
value is not defined in the rule.
Comment: Commenters stated that time is needed to install
continuous monitors and to make other necessary changes (such as
installing a flare gas recovery system or additional amine treatment)
to comply with all the flare requirements (e.g., limiting short-term
H2S concentration to 162 ppmv, long-term 60 ppmv
H2S fuel gas concentration limit, flare management plan,
root cause analysis and continuous monitoring), especially considering
how quickly a flare may become a modified affected source. While most
commenters focused on the amount of time needed to install equipment to
comply with the long-term 60 ppmv H2S fuel gas concentration
limit, other commenters asserted that additional time for activities,
such as planning and re-piping, would be needed to meet the standards.
Commenters requested differing amounts of additional time generally
ranging from 3 to 5 years. Commenters noted that the additional time
would allow owners and operators to schedule any process unit shutdowns
needed to install new equipment or monitors during a turnaround. One
commenter recommended that the extra time to begin root cause analyses
provided to refiners committing to install flare gas recovery systems
should also be provided to refiners committing to expand an existing
flare gas recovery system. Commenters also noted that experience
implementing SCAQMD Rule 1118 suggests that there will be difficulty
obtaining and installing continuous monitors in less than 3 years due
to the availability of monitor manufacturers and the need to stage the
installation of monitors at refineries with multiple affected flares.
One commenter requested that the EPA consider a compliance schedule in
40 CFR part 60, subpart Ja that is consistent with compliance schedules
in consent decrees. Commenters objected to phasing out the additional
time after the rule has been in place for 5 years.
One commenter requested clarification regarding the trigger date
from which the additional time to comply with the flare provisions
(e.g., 2 years when installing a flare gas recovery system) begins. The
commenter questioned whether the trigger date is when construction
starts, at startup or when the stay is removed (or whichever is later).
Another commenter agreed that the EPA should
[[Page 56450]]
set the compliance time based on the initial startup of the
modification. The commenter noted that the EPA should follow the 40 CFR
part 60 General Provisions for performance test timing and the 40 CFR
part 63 General Provisions for compliance timing.
Response: As we are no longer applying the long-term 60 ppmv
H2S fuel gas concentration limit to flares, the comments
related to the amount of time needed to comply with a long-term 60 ppmv
H2S fuel gas concentration limit are moot. We do, however,
recognize that a flare modification can occur much more quickly than
modifications of traditional process-related emission sources.
Therefore, we evaluated the comments regarding the amount of time
needed to meet the various requirements for flares while keeping the 40
CFR part 60, subpart Ja flare modification provision in mind. We
discuss each requirement and the time for demonstrating compliance with
that requirement in the following paragraphs.
We find it appropriate to require modified flares that already have
adequate treatment and monitoring equipment in place to achieve a
short-term H2S concentration of 162 ppmv (resulting from
compliance with 40 CFR part 60, subpart J) to continue to meet that
concentration upon startup of the affected flare or the effective date
of this final rule, whichever is later. However, some flares are not
affected facilities subject to 40 CFR part 60, subpart J, and others
are complying with subpart J requirements as specified in consent
decrees or have received alternative monitoring plans by which to
demonstrate compliance with the short-term H2S concentration
limit. In these cases, we find it appropriate to allow more time to
comply with the short-term H2S concentration limit and/or
the associated monitoring requirements because additional amine
treatment and/or monitoring systems will be required to comply with the
rule.
Therefore, the final rule requires all modified flares that are
newly subject to 40 CFR part 60, subpart Ja (but were not previously
subject to 40 CFR part 60, subpart J) to comply with the short-term
H2S concentration limit and applicable monitoring
requirements no later than 3 years after the effective date of this
final rule or upon startup of the affected flare, whichever is later.
Modified flares that have accepted applicability of subpart J under a
federal consent decree shall comply with the subpart J requirements as
specified in the consent decree but shall comply with the short-term
H2S concentration limit and applicable monitoring
requirements no later than 3 years after the effective date of this
final rule. Modified flares that are already subject to the 162 ppmv
short-term H2S concentration limit under subpart J must meet
the short-term H2S concentration limit under subpart Ja upon
startup of the affected flare or the effective date of this final rule,
whichever is later. Finally, modified flares that are already subject
to the short-term H2S concentration limit but that have an
approved monitoring alternative under subpart J and do not have the
monitoring equipment in-place that is required under subpart Ja shall
be given up to 3 years from the effective date of this final rule to
install the monitors required by subpart Ja (or to obtain an approved
monitoring alternative under subpart Ja).
As we noted in the preamble to the proposed amendments, many of the
connections that would trigger applicability to 40 CFR part 60, subpart
Ja are critical to the safe and efficient operation of the refinery.
These connections can, and often must, be installed quickly. At the
same time, nearly all refineries will need time for planning,
designing, purchasing and installing (including any necessary re-
piping) sulfur and flow monitors that are newly required by subpart Ja.
Some refineries will elect to add flare gas recovery and/or sulfur
treatment equipment to minimize their emissions as part of the
evaluations conducted, as required by the new flare management plan
requirements, and time will be needed for planning, designing,
purchasing and installing these components as well. Given that many
flares will become modified affected sources relatively quickly, owners
and operators will be competing with one another for the services and
products of a finite number of vendors who provide the necessary
monitors and other equipment. Several commenters specifically noted
availability of monitors as an issue when complying with SCAQMD Rule
1118. As such, we find that immediate compliance with the requirements
for flares, such as the planning, designing, purchasing and
installation of (including any necessary re-piping) sulfur and flow
monitors, may be difficult for operators to meet, especially in
situations where quick connections to the flare are made. A phased
compliance schedule allows for the operators to comply with some
requirements associated with flares, such as continuing to achieve a
short-term H2S concentration of 162 ppmv, if the flares are
already subject to 40 CFR part 60, subpart J and have adequate
monitoring in place to comply with this final rule, while allowing time
to install treatment and processing equipment and monitoring equipment
to comply with the standards where necessary.
A phased compliance schedule will also allow owners and operators
to minimize process interruption by coordinating the installation of
monitoring equipment with process shutdowns or turnarounds. In addition
to providing operating flexibility to the refinery, we are taking into
consideration the fact that a process shutdown and subsequent startup
can generate significant emissions, even if the refinery is taking care
to minimize those emissions. We consider a phased compliance schedule
that allows owners and operators to avoid startups and shutdowns that
are not necessary to maintain the equipment and process to be
environmentally beneficial overall and the best system of emissions
reduction for a quickly modified flare. Considering the time needed to
complete engineering specifications, order and install the required
monitoring equipment, and considering the need to coordinate this
installation with process unit shutdown or turnarounds, we determined
that completion of these activities within 3 years is consistent with
the best system of emissions reductions for quickly modified flares.
We note, however, that this phased compliance schedule for the
flare requirements in 40 CFR part 60, subpart Ja is intended for those
situations when a flare modification occurs quickly and the owner or
operator does not have significant planning opportunities to install
the required monitors or implement the selected flare minimization
options without significant process interruptions. For a future large
project on a schedule that includes time for planning, designing,
purchasing and installing equipment and monitors, we expect that the
owner and operator will have time to assess whether or not the refinery
flares will become affected sources through modification. If a project
will result in the modification of a flare, we expect that the owner or
operator will then plan how to meet the standards in subpart Ja as part
of the project itself, including the installation of the monitoring
systems and the development of a flare management plan. Because of the
ability to plan ahead, flares that are modified as part of a large
project will not have all of the difficulties meeting the subpart Ja
flare requirements upon completion of the modification as those flares
that are modified quickly. Therefore, we find that compliance with the
flare
[[Page 56451]]
requirements upon startup of the modified flare is appropriate and
consistent with the best system of emissions reduction for large
projects resulting in a modification of a flare. Thus, we determined
that the appropriate time period for compliance with the flare
standards is either: (1) 3 years from the effective date of these
amendments or (2) upon startup of the modified flare, whichever is
later.\11\ In this manner, flares that become subject to subpart Ja
quickly, based on a small safety-related connection (or have already
become subject to subpart Ja based on a modification prior to the
effective date of these amendments), will have up to 3 years from the
effective date of these amendments to comply fully with the flare
standards, but flares that are modified as the result of a significant
project, such as the installation of a new process unit that will be
tied into an existing flare, will effectively be required to comply
with the flare standards at the startup of the new process unit.
---------------------------------------------------------------------------
\11\ For the purposes of this subpart, startup of the modified
flare occurs when any of the activities in 40 CFR 60.100a(c)(1) or
(2) is completed (e.g., when a new connection is made to a flare
such that flow from a refinery process unit or ancillary equipment
can flow to the flare via that new connection).
---------------------------------------------------------------------------
Therefore, for the reasons described above, we are providing flares
that become affected facilities subject to 40 CFR part 60, subpart Ja
through modification with a phased compliance schedule for the flare
standards, as described in this paragraph. The final rule requires
owners and operators of modified flares to meet the short-term 162 ppmv
H2S concentration requirement by the effective date of these
amendments or upon startup of the affected flare (whichever is later)
only if they are already subject to the short-term 162 ppmv
H2S concentration limit in 40 CFR part 60, subpart J.
Modified flares that were not affected flares under subpart J prior to
being modified facilities under subpart Ja must comply with the short-
term 162 ppmv H2S concentration requirement within 3 years
of the effective date of these amendments or upon startup of the
modified flare, whichever is later. Owners and operators of modified
flares that are have accepted applicability of subpart J under a
federal consent decree shall comply with the subpart J requirements as
specified in the consent decree, but must meet the short-term 162 ppmv
H2S concentration limit no later than 3 years after the
effective date of this final rule. Owners and operators of modified
flares that are already subject to subpart J and that have an approved
monitoring alternative and are unable to meet the applicable subpart Ja
monitoring requirements for the short-term H2S concentration
limit must meet the short-term H2S concentration requirement
upon startup of the affected flare or the effective date of this final
rule, whichever is later, but shall be given up to 3 years from the
effective date of this final rule to install the monitors required by
subpart Ja. In this interim period, owners and operators of these
modified flares shall demonstrate compliance with the short-term
H2S concentration limit using the monitoring alternative
approved under subpart J.
Additionally, we are requiring owners and operators of modified
flares to complete and implement the flare management plan under 40 CFR
60.103a(a) by 3 years from the effective date of these amendments or
upon startup of the modified flare, whichever is later. We are
requiring owners and operators of modified flares to begin conducting
root cause and corrective action analyses under 40 CFR 60.103a(c) and
(d) no later than 3 years from the effective date of these amendments
or the date of the startup of the modified flare, whichever is later,
so that the facility can complete the flare management plan and
establish baseline flow rates prior to performing the root cause and
corrective action analyses. We are also requiring owners and operators
of modified flares to install and begin operating the monitors
necessary to demonstrate compliance with these provisions, as required
under 40 CFR 60.107a(e) through (g) within 3 years from the effective
date of these amendments or by the startup date of the modified flare,
whichever is later, when the monitors are not already in place.
Compliance with the phased compliance schedule constitutes compliance
with the flare standards as of the effective date.
We note that the final rule does not provide a phased compliance
schedule for new and reconstructed flares. The final rule requires
owners and operators of new and reconstructed flares to meet all the
flare requirements, including the short-term 162 ppmv H2S
concentration requirement, upon the effective date of the requirements
or upon startup of the affected flare, whichever is later.
C. Other Comments
Comment: Several commenters objected to the change to the
definition of ``refinery process unit.'' The commenters objected to the
proposed amendments to include coke gasification, loading and
wastewater treatment, stating the change makes the term more expansive.
The commenters stated that the EPA did not evaluate the impacts or
explain the consequences of the revised definition. One commenter
stated that product loading is generally considered part of the
refinery process unit to which it is associated and that wastewater
treatment is a utility. Another commenter suggested that the definition
specify SIC 2911 (as in Refinery MACT 1).
Response: The original definition of ``refinery process unit'' in
40 CFR part 60, subpart J and the definition of ``refinery process
unit'' promulgated in 40 CFR part 60, subpart Ja in June 2008 read as
follows: ``Refinery process unit means any segment of the petroleum
refinery in which a specific processing operation is conducted.'' Thus,
to be considered a refinery process unit, only two criteria are needed:
(1) The unit must be located at a petroleum refinery; and (2) the unit
must be used to conduct ``a specific processing operation.'' The
definition does not directly limit the scope of ``processing
operations.'' That is, the definition of refinery process unit does not
limit process operations to distillation, re-distillation, cracking or
reforming, and it is not limited to only those processes used to
produce gasoline, kerosene, fuel oils, etc. In the proposed amendment
to this definition, we listed ``operations'' that we construed as
conducting a ``specific processing operation'' when these operations
are located at a petroleum refinery. Consequently, we considered the
proposed inclusion of examples of refinery process units to be a
clarification of the existing definition rather than an expansion of
the original definition.
We reviewed the impact of the proposed revision of this definition
on 40 CFR part 60, subpart Ja, as well as its historic use in 40 CFR
part 60, subpart J. The term ``refinery process unit'' is used
primarily in the definitions of certain affected facilities, ``process
gas'' and ``process upset gas'' in subparts J and Ja. The term is also
used in the flare provisions in subpart Ja. With respect to the
definitional terms, there can be no issue with including the
designation of ``refinery process unit'' within the definitions for
specific process units. ``Process gas'' is not used at all in either
rule, although it was revised between proposal and promulgation of
subpart J. In response to a comment that the definition of ``process
gas'' ``should have included the non-hydrocarbon gases produced by
various process units in a refinery,'' the EPA responded: ``The
definition has been revised to include all gases produced by process
units in a refinery except fuel gas and process upset gas.'' (See page
127 of Background
[[Page 56452]]
Information for New Source Performance Standards, Volume 3, Promulgated
Standards (BID Vol. 3), EPA 450/2-74-003 (Feb. 1974), Docket Item No.
EPA-HQ-OAR-2007-0011-0082). The definition had actually been revised to
include ``any gas generated by a petroleum refinery process unit.'' The
response in BID Vol. 3 suggests that the EPA considered ``refinery
process units'' and ``process units in a refinery'' to have the same
meaning, and there is no mention of limiting what is considered to be a
``refinery process unit'' or a ``process units in a refinery.''
``Process upset gas'' is used only to provide an exemption to the
H2S concentration limit for process upset gas sent to a
flare. See 40 CFR 60.104(a)(1), 60.103a(h). Therefore, a narrow
definition of ``refinery process unit'' would only limit those gases
sent to a flare that would qualify as ``process upset gas.'' For
example, if a coke gasifier is not a refinery process unit, then gases
generated during the startup, shutdown or malfunction of a coke
gasifier located at the refinery would not be ``process upset gas'' and
would be required to comply with the requirement to limit short-term
H2S concentration in fuel gas to 162 ppmv if sent to a
flare. We find that the historical application of the ``process upset
gas'' exclusion has considered a broad definition of what constitutes a
``refinery process unit.''
For 40 CFR part 60, subpart Ja, the definition of ``refinery
process unit'' also impacts the flare provisions. Based on the proposed
revisions of ``refinery process unit,'' it was clearly our intent that
a broad definition of ``refinery process unit'' should apply to the
flare requirements. Specifically, we intended that a flare modification
occurs when a wide range of equipment at the petroleum refinery is
newly connected to the flare. It was also our intent that the flare
management plan consider flare minimization methods for this broadly
defined range of equipment referred to collectively as ``refinery
process units.''
Based on our review of the impacts of changes to the definition of
``refinery process unit,'' and considering all of the comments
received, we maintain that the existing definition of ``refinery
process unit'' is broad and should be broadly interpreted. For
consistency between 40 CFR part 60, subparts J and Ja, we have elected
to maintain the existing definition and not include an example list of
refinery process units within the definition. However, to clarify that
a modification to a flare occurs when these types of equipment are
connected to the flare, we revised the language in the flaring
provisions to refer to ``refinery process units, including ancillary
equipment.'' This revision is made to clarify our original intent that
coke gasification units, storage tanks, product loading operations and
wastewater treatment systems, as well as pressure relief valves, pumps,
sampling vents, continuous analyzer vents and other similar equipment
are units from which a connection to a flare would trigger a flare
modification and generate gas streams that should be considered in the
flare management plan. We have included in the final amendments a
definition of ``ancillary equipment.'' Specifically, ancillary
equipment means equipment used in conjunction with or that serve a
refinery process unit. Ancillary equipment includes, but is not limited
to, storage tanks, product loading operations, wastewater treatment
systems, steam- or electricity-producing units (including coke
gasification units), pressure relief valves, pumps, sampling vents, and
continuous analyzer vents.
Sulfur recovery plants are also units from which a connection to a
flare would trigger a flare modification and generate gas streams that
should be considered in the flare management plan. We recognize that
on-site sulfur recovery plants are considered refinery process units,
and we proposed amendments to the definitions of ``refinery process
unit'' and ``sulfur recovery plant'' to clarify that we consider a
sulfur recovery plant to be ``a segment of the petroleum refinery in
which a specific processing operation is conducted.'' However, the
strict definition of ``refinery process unit'' would only apply to
sulfur recovery plants physically located at the refinery. As 40 CFR
part 60, subpart Ja also applies to off-site sulfur recovery plants
(see 40 CFR 60.100(a) and 40 CFR 60.100a(a)), we found it potentially
contradictory to define a sulfur recovery plant located outside the
refinery as a ``refinery process unit,'' so we are also not finalizing
the proposed amendment to include the term ``all refinery process
units'' in the definition of ``sulfur recovery plant.'' However, while
connections to a refinery flare from an off-site sulfur recovery plant
are not expected to be common, off-site sulfur recovery plants are
subject to subpart Ja. We clarify in this response that we would
consider such a connection to a flare to be from a ``refinery process
unit, including ancillary equipment,'' such that connecting an off-site
sulfur recovery plant that is subject to subpart Ja to a flare at a
refinery would cause that flare to be a modified flare subject to
subpart Ja.
Further, in reviewing the definition of ``sulfur recovery plant,''
we noticed an inadvertent error that also suggests that the sulfur
recovery plant must be located at a petroleum refinery, which is not
consistent with the applicability provisions in 40 CFR 60.100(a) and 40
CFR 60.100a(a). Specifically, we inadvertently omitted the word
``produced'' in this first sentence, so we are amending the definition
of ``sulfur recovery plant'' to clarify that a sulfur recovery plant
recovers sulfur from sour gases ``produced at the petroleum refinery.''
Thus, we are amending the definition of ``sulfur recovery plant'' to
correct inadvertent errors and to clarify that off-site sulfur recovery
plants are included in the definition of ``sulfur recovery plant,'' as
these plants are expressly considered to be affected facilities in 40
CFR part 60, subpart Ja.
Comment: Commenters supported the revised definition of ``delayed
coking unit,'' but stated that, since 40 CFR part 60, subpart Ja only
sets standards for the coke drums, the definition should just include
the coke drums associated with a single fractionator. The commenters
stated that the definition should not include the fractionator itself
because VOC emissions from the fractionator are covered by NSPS for
equipment leaks.
Response: The proposed amendments to the definition of ``delayed
coking unit'' specifically listed the primary components of the delayed
coking unit. In particular, based on the operation of the delayed
coking unit, we find that the fractionator is an integral part of the
delayed coking unit. The fresh feed to the delayed coking unit is
generally introduced in the fractionator tower bottoms receiver. This
integral use of the fractionator is different than the use of
fractionators used for other units defined in 40 CFR part 60, subpart
Ja, such as the fluid catalytic cracking unit (FCCU). For the FCCU,
fresh feed is introduced in the riser, which is part of the affected
facility in subpart Ja. As the feed to the delayed coking unit is to
the fractionator, we find that the fractionator is an integral part of
the delayed coking unit, so we specifically include it as part of the
affected facility. While our proposed amendments covered only the major
components of the delayed coking unit, upon our review of the
definition based on the comments received, we note that there are
several other components of the delayed coking unit that are integral
to the operation of the delayed coking unit. Additionally, even though
the standards are specific to the coke drum, many of these integral
components are
[[Page 56453]]
interconnected and necessary for the delayed coking unit to meet the
applicable standards. Based on our review of the operation of a delayed
coking unit, we also include coke cutting and blowdown recovery
equipment in the final definition because this equipment is also
integral to the overall cyclical operation of the process unit. The
definition of ``delayed coking unit'' has been amended in the final
rule to mean a refinery process unit in which high molecular weight
petroleum derivatives are thermally cracked and petroleum coke is
produced in a series of closed, batch system reactors. A ``delayed
coking unit'' includes, but is not limited to all of the coke drums
associated with a single fractionator; the fractionator, including
bottoms receiver and overhead condenser; the coke drum cutting water
and quench system, including the jet pump and coker quench water tank;
process piping and associated equipment such as pumps, valves and
connectors; and the coke drum blowdown recovery compressor system.
Since this definition is more specific than the definition included
in the amendments proposed on December 22, 2008, it could affect which
delayed coking units are subject to subpart Ja. For example, an owner
or operator may have made a change to a delayed coking unit that would
not be considered a modification under the December 22, 2008,
definition, but that same change could make the delayed coking unit a
modified facility subject to subpart Ja using the definition of
``delayed coking unit'' above. In other words, in changing the
definition of ``delayed coking unit'' in the final rule, some delayed
coking units that would not have been affected sources under the
proposed requirements might now be covered by the final rule. Under CAA
section 111(a)(2), a ``new source'' is defined from the date of
proposal only if there is a standard ``which will be applicable to such
source;'' otherwise, a ``new source'' is defined based upon the final
rule date. In this circumstance, using the proposal date as the new
source date for determining applicability for this group of delayed
coking units would be inappropriate as such units would not have been
on notice that subpart Ja could apply to them. Accordingly, we moved
the ``new source'' date for this group of delayed coking units so that
delayed coking units that are only defined as such under the final rule
are covered by the final rule only if they commence construction,
reconstruction or modification after the promulgation date of these
final amendments. The ``new source'' date for other delayed coking
units will depend on the previous definitions and when the activities
involving the delayed coking unit occurred. See Sec. 60.100a(b) for
determining applicability of subpart Ja for delayed coking units.
Comment: One commenter stated that 40 CFR part 63, subpart LLLLL
indicates at 40 CFR 63.8681(e) that 40 CFR part 60, subpart J does not
apply for asphalt blowing stills subject to subpart LLLLL, and the
commenter requested similar clarification for 40 CFR part 60, subpart
Ja by exempting this process in 40 CFR 60.100a.
Response: We reviewed the requirement in 40 CFR part 63, subpart
LLLLL. Due to the O2 content of this process gas, we agree
that it is not suitable for recovery as fuel gas and subsequent amine
treatment; therefore, it is not BSER for combustion controls used on
asphalt blowing stills to meet the H2S concentration limits
(or alternative SO2 emissions limits). We reviewed 40 CFR
60.100a, but we feel a blanket exemption from 40 CFR part 60, subpart
Ja is not necessary. Instead, we have included an exemption within the
definition of fuel gas similar to the exemptions included for
combustion controls on vapors collected and combusted from wastewater
treatment and marine vessel loading operations. Specifically, we
amended the definition of fuel gas in 40 CFR 60.101a to clarify that
fuel gas does not include vapors that are collected and combusted to
control emissions from asphalt processing units (i.e., asphalt blowing
stills).
Comment: One commenter recommended that the exclusion from the
definition of ``fuel gas'' be extended to vapors ``from marine vessel
loading operations or waste management units that are collected and
combusted'' without any reference to a federal requirement. At a
minimum, the commenter stated that marine benzene loading under 40 CFR
part 61, subpart BB; the wastewater provisions of 40 CFR part 63,
subpart G; remediation efforts regulated under Resource Conservation
and Recovery Act (RCRA) corrective action; and RCRA 7003 orders should
be added to the exclusion.
Response: We were originally concerned that removing the reference
to a federal standard may inadvertently exempt the use of these vapors
when used in process heaters or boilers. We determined that it was not
BSER to require thermal oxidizers used to comply with the cited federal
standards to comply with the H2S concentration limits due to
the typically remote location of the combustion sources (control
devices) relative to refinery process units (see technical memorandum
entitled Fuel Gas Treatment of Marine Vessel Loading and Wastewater
Treatment Unit Off-gas, in Docket ID No. EPA-HQ-OAR-2007-0011).
However, if these gases are currently routed to a fuel gas system or
directly to a process heater or boiler, treatment of the fuel gas to
meet the SO2 emissions limits or the H2S
concentration limits is expected to be economically viable.
Additionally, these gases are expected to be only a small portion of
the fuel gas combusted in these units, and the refinery has an option
to over-treat the primary fuel gas so that gases from the wastewater
treatment system or marine vessel loading operation can remain
untreated while the fuel gas combustion device itself can comply with
the SO2 emissions limits or the H2S concentration
limits, based on the mixture of fuels used in the device.
In reviewing the rules suggested by the commenter, as well as those
we originally listed, we noted that acceptable ``control devices'' or
``combustion units'' in these rules include process heaters and
boilers. We did not intend to exclude vapors that are collected and
routed to a process heater or boiler to be exempt from the definition
of fuel gas. In other words, when developing this exclusion, we
specifically considered the combustion of these gases via a thermal
oxidizer or flare currently located at the marine vessel loading or
wastewater treatment location. These remote combustion devices were
really the subject of the analysis, but we did not want to exclude
these combustion units themselves because other fuel gas is often fed
to these units to ensure adequate combustion of the vapors being
controlled. It is clear from our rationale and the description of the
exemption included in the preamble of the proposed rule that the
exemption was intended ``to exempt vapors that are collected and
combusted in an air pollution control device installed to comply with''
specific wastewater or marine vessel loading emissions standards. (72
FR 27180 and also at 27183) Process heaters or boilers would not be
``installed'' to comply with these provisions, and it was not our
intent to exclude vapors sent to these types of combustion units.
However, the regulatory text is more ambiguous and appears to exclude
any vapors collected and combusted, regardless of where they are
combusted. As such, we are amending this exclusion to better represent
our original intent.
[[Page 56454]]
Additionally, with the added clarity in the regulatory text, it
seems appropriate to extend this exclusion to control devices used at
these locations regardless of why the emission controls were installed.
That is, while we originally considered air pollution control devices
that were mandated by the EPA, we see no reason to discriminate against
air pollution control devices that were installed voluntarily to reduce
the emissions from these sources. Further, we intend to clarify that
gases off the sour water system, including the sour water stripper,
would likely contain higher amounts of reduced sulfur and would be
economically viable to treat. Therefore, we are also clarifying that
the exemption does not extend to the sour water system. Therefore, the
amended definition of ``fuel gas'' in both 40 CFR part 60, subparts J
and Ja states that fuel gas ``does not include vapors that are
collected and combusted in a thermal oxidizer or flare installed to
control emissions from wastewater treatment units other than those
processing sour water, marine tank vessel loading operations, or
asphalt processing units (i.e., asphalt blowing stills).''
With respect to remediation efforts conducted under RCRA corrective
actions, we are unwilling to grant such an exclusion from the
definition of ``fuel gas'' in 40 CFR part 60, subpart Ja. First, we
anticipate that most vapors from remediation efforts would be low in
sulfur and, if so, the owner or operator could apply for the
alternative monitoring methods provided in the rule. Also, although
some remediation efforts may occur in remote locations, many of the
remediation efforts are conducted in reasonable proximity to existing
process units. Finally, the range of activities included in RCRA
remediation efforts is broad, and we have little information regarding
the number and types of RCRA remediation activities that are being
conducted. The commenter provided no description of such activities,
nor did they provide a reasonable rationale as to why the vapors from
these activities should be exempted.
V. Summary of Cost, Environmental, Energy and Economic Impacts
A. What are the emission reduction and cost impacts for the final
amendments?
The emission reduction and cost impacts presented in this section
for flares are revised estimates for the impacts of the final
requirements of 40 CFR part 60, subpart Ja for flares, as amended by
this action. The table shows the differences in anticipated impacts
between these final amendments to subpart Ja and the final June 2008
NSPS requirements of subpart Ja, which were estimated assuming only 40
flares would trigger applicability to the rule. The impacts are
presented for 400 affected flares that commence construction,
reconstruction or modification that will be required to comply with
this final rule. We anticipate that most of the flares would become
affected due to the modification provisions for flares set forth in the
final June 2008 subpart Ja rule. For this analysis, we assumed that 90
percent of the flares will be modified or reconstructed and 10 percent
of the flares will be newly constructed. Further, we estimate that 30
percent of the 400 affected flares, or 120 flares, either would meet
the definition of ``emergency flare'' in subpart Ja or would be
equipped with a flare gas recovery system such that robust sulfur and
flow monitoring would not be required. Therefore, the values in Table 5
of this preamble include the costs and emissions reductions for 400
flares to comply with the flare management plan and root cause and
corrective action analyses requirements and for 280 flares to comply
with the sulfur and flow monitoring requirements. The cost and
emissions reductions for the affected flares to comply with the short-
term H2S concentration of 162 ppmv in the fuel gas are
included in the baseline rather than the incremental impacts because
this limit is unchanged from the requirements in 40 CFR part 60,
subpart J. For further detail on the methodology of these calculations,
see Documentation of Impact Estimates for Fuel Gas Combustion Device
and Flare Regulatory Options for Amendments to the Petroleum Refinery
NSPS, in Docket ID No. EPA-HQ-OAR-2007-0011.
We estimate that the final requirements for flares will reduce
emissions of SO2 by 3,200 tons/yr, NOX by 1,100
tons/yr and VOC by 3,400 tons/yr from the baseline. The estimated
annual cost, including annualized capital costs, is a cost savings of
about $79 million (2006 dollars) due to the replacement of some natural
gas purchases with recovered flare gas and the retention of
intermediate and product streams due to a reduction in the number of
malfunctions associated with refinery process units and ancillary
equipment connected to the flare. Note that not all refiners will
realize a cost savings since we only estimate that refineries with high
flare flows will install vapor recovery systems. Although the rule does
not specifically require installation of flare gas recovery systems, we
project that owners and operators of flares receiving high waste gas
flows will conclude, upon installation of monitors, implementation of
their flare management plans, and implementation of root causes
analyses, that installing flare gas recovery would result in fuel
savings by using the recovered flare gas where purchased natural gas is
now being used to fire equipment such as boilers and process heaters.
The flare management plan requires refiners to conduct a thorough
review of the flare system so that flare gas recovery systems are
installed and used where these systems are warranted. As part of the
development of the flare management plan, refinery owners and operators
must provide rationale and supporting evidence regarding the flare
waste gas reduction options considered, the quantity of flare gas that
would be recovered or prevented by the option, the BTU content of the
flare gas and the ability or inability of the reduction option to
offset natural gas purchases. In addition, consistent with Executive
Order 13563 (Improving Regulation and Regulatory Review, issued on
January 18, 2011), for facilities implementing flare gas recovery, we
are finalizing provisions that would allow the owner or operator to
reduce monitoring costs and the number of root cause analyses,
corrective actions, and corresponding recordkeeping and reporting they
would need to perform. We estimate that the final requirements for
flares will reduce emissions of SO2 by 3,200 tons/yr,
NOX by 1,100 tons/yr and VOC by 3,400 tons/yr from the
baseline. The overall cost effectiveness is a cost savings of about
$10,000 per ton of combined pollutants removed. The estimated
nationwide 5-year emissions reductions and cost impacts for the final
standards are summarized in Table 5 of this preamble.
[[Page 56455]]
Table 5--National Emission Reductions and Cost Impacts for Petroleum Refinery Flares Subject to Amended Standards Under 40 CFR part 60, subpart Ja
[Fifth year after the effective date of these final rule amendments] \a\
--------------------------------------------------------------------------------------------------------------------------------------------------------
Natural gas
Total Total offset/ Total Annual Annual Annual Cost
capital annual cost product annual cost emission emission emission effectiveness
Subpart Ja requirements cost without recovery ($1,000/ reductions reductions reductions ($/ton
($1,000) credit credit yr) (tons SO2/ (tons NOX/ (tons VOC/ emissions
($1,000/yr) ($1,000) yr) yr) yr) reduced)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Estimates from June 2008 Final Rule......... 40,000 ........... ........... (7,000) 80 6 200 (23,000)
Revised Estimates for Amendments............ 460,000 100,000 (180,000) (79,000) 3,200 1,100 3,400 (10,000)
--------------------------------------------------------------------------------------------------------------------------------------------------------
\a\ All costs in this table are relative to the baseline used for the 2008 final rule.
We also estimate that the final requirements for flares will result
in emissions reduction co-benefits of CO2 equivalents by
1,900,000 metric tonnes per year, predominantly as a result of our
estimate of the largest flares employing flare gas recovery and to a
lesser extent, as a result of the root cause analyses applicable to all
flares.
The cost, environmental and economic impacts for the final
amendments to 40 CFR part 60, subpart Ja for process heaters are not
expected to be different than those reported for the final June 2008
standards. We expect owners and operators to install the same
technology to meet these final amendments that we anticipated they
would install to meet the June 2008 final subpart Ja requirements
(i.e., ultra-low NOX burners). We did revise our emission
estimates based on the type of process heater, creating separate
impacts for forced draft process heaters and natural draft process
heaters. Dividing process heaters into separate subcategories, based on
the draft type, required us to develop new distributions of baseline
emissions for each type of process heater. The baseline emission
estimates for natural draft process heaters are slightly lower than
those developed for the existing subpart Ja requirements (per affected
process heater), but the average emission reduction achieved by ultra-
low NOX burners was adjusted to 80 percent (rather than 75
percent used for generic process heaters). For forced draft process
heaters, the baseline (i.e., uncontrolled) emissions rate for forced
draft process heaters was revised slightly upward, based on the
available emissions data. Due to these differences, the mix of controls
needed to meet a 40 ppmv emissions limit was no longer cost effective
for forced draft process heaters, but the emission reductions
associated with process heaters complying with the 60 ppmv standard
were higher than those previously estimated for generic process
heaters. Thus, the creation of new subcategories of process heaters
with different emissions limits for each subcategory did not impact the
control or compliance methods used by the facilities (i.e., BSER in all
cases was based on the performance of advanced combustion monitoring
controls in conjunction with ultra-low NOX burners) and did
not change the estimated compliance costs. As we do not have adequate
data regarding the prevalence of natural draft process heaters versus
forced draft process heaters that will become subject to the rule, we
used the emission reductions estimated for the two different types of
process heaters as a means to bound the range of anticipated
NOX emission reductions to be from 7,100 to 8,600 tons/yr in
the fifth year after the effective date of this final rule (see Revised
NOX Impact Estimates for Process Heaters, in Docket ID No.
EPA-HQ-OAR-2007-0011). We estimated the emission reductions to be 7,500
tons/yr for the June 2008 final standards, which falls well within the
anticipated range of emissions reductions for the standards we are
finalizing here. Given the uncertainty in the emissions estimates, as
well as the uncertainty in the relative number of natural draft process
heaters versus forced draft process heaters, we concluded that the
impacts previously developed for subpart Ja accurately represent the
impacts for process heaters in these final amendments.
We note that, in the preamble to the June 2008 final standards, we
estimated costs and emissions reductions for 30 fuel gas combustion
devices, but we subsequently determined that those estimates did not
fully account for the number of affected flares (which, at the time,
were considered a subset of fuel gas combustion devices). Therefore, in
the preamble to the December 2008 proposed amendments, we presented
revised emission reduction and cost estimates for affected fuel gas
combustion devices. As previously explained, we are not finalizing the
long-term 60 ppmv H2S fuel gas concentration limit for
flares, as proposed, and we revised our cost estimates accordingly.
Because these final amendments consider flares to be a separate
affected source, the emission reductions and costs for fuel gas
combustion devices are not affected by these final amendments and are
not included in this preamble. Rather, the final emission reduction and
cost estimates for fuel gas combustion devices are very close to the
impacts presented in the June 2008 final rule; the details of the
analysis and the final impacts are presented in Documentation of Impact
Estimates for Fuel Gas Combustion Device and Flare Regulatory Options
for Amendments to the Petroleum Refinery NSPS, in Docket ID No. EPA-HQ-
OAR-2007-0011.
The final amendments to 40 CFR part 60, subpart J are technical
corrections or clarifications to the existing rule and should have no
negative emissions impacts.
B. What are the economic impacts?
The total annualized compliance costs are estimated to save about
$79 million (2006 dollars) in the fifth year after the effective date
of these final amendments. Note that not all refiners will realize a
cost savings as only flare systems with high waste gas flows (about 10
percent of all flares) are expected to install vapor recovery systems.
Alternatively, if no refineries install flare gas recovery systems,
total annualized compliance costs are estimated to be $10.7 million
(2006 dollars) in the fifth year after proposal. Regardless of whether
any refineries install flare gas recovery systems, we do not anticipate
any adverse economic impacts associated with this regulatory action, as
no increase in refined petroleum product prices or decrease in refined
petroleum product output is expected.
[[Page 56456]]
For more information, please refer to the Regulatory Impact
Analysis (RIA) that is in the docket for this final rule.
C. What are the benefits?
Emission controls installed to meet the requirements of this rule
will generate benefits by reducing emissions of criteria pollutants and
their precursors, including SO2, NOX and VOC as
well as CO2. SO2, NOX and VOC are
precursors to PM2.5 (particles smaller than 2.5 microns),
and NOX and VOC are precursors to ozone. For this rule, we
were only able to quantify the health benefits associated with reduced
exposure to PM2.5 from emission reductions of SO2
and NOX and the climate benefits associated with
CO2 emission reductions. We estimate the monetized benefits
of this final regulatory action to be $270 million to $580 million
(2006 dollars, 3-percent discount rate) in the fifth year (2017). The
benefits at a 7-percent discount rate for health benefits and 3-percent
discount rate for climate benefits are $240 million to $530 million
(2006 dollars). For small flares only, we estimate the monetized
benefits are $170 million to $410 million (3-percent discount rate) and
$150 million to $370 million (7-percent discount rate for health
benefits and 3-percent discount rate for climate benefits). For large
flares only, we estimate the monetized benefits are $93 million to $160
million (3-percent discount rate) and $88 million to $150 million (7-
percent discount rate for health benefits and 3-percent discount rate
for climate benefits). Using alternate relationships between
PM2.5 and premature mortality supplied by experts, higher
and lower benefits estimates are plausible, but most of the expert-
based estimates fall between these two estimates.\12\ A summary of the
monetized benefits estimates by pollutant for all flares at discount
rates of 3 percent and 7 percent is in Table 6 of this preamble.
Several benefits categories, including direct exposure to
SO2 and NOX benefits, ozone benefits, ecosystem
benefits and visibility benefits are not included in these monetized
benefits. All estimates are in 2006 dollars for the year 2017.
---------------------------------------------------------------------------
\12\ Roman, et al., 2008. Expert Judgment Assessment of the
Mortality Impact of Changes in Ambient Fine Particulate Matter in
the U.S., Environ. Sci. Technol., 42, 7, 2268--2274.
Table 6--Summary of the Monetized PM2.5 and CO2 Benefits for Amended Petroleum Refineries Standards
[Millions of 2006 dollars] \a\
----------------------------------------------------------------------------------------------------------------
Total monetized Total monetized
Pollutant Emission reductions benefits (3-percent benefits (7-percent
(tons per year) discount) discount)
----------------------------------------------------------------------------------------------------------------
With Flare Gas Recovery
----------------------------------------------------------------------------------------------------------------
PM2.5 Benefits\b\:
SO2.............................. 3,200.................. $210 to $510........... $190 to $460.
NOX.............................. 1,100.................. $7.1 to $18............ $6.4 to $16.
PM Total......................... ....................... $220 to $530........... $190 to $480.
CO2 Benefits\c\.................. 1,900,000\d\........... $46.................... $46.
--------------------------------------------------------------------------
Total Monetized Benefits:.... ....................... $260 to $580........... $240 to $520.
----------------------------------------------------------------------------------------------------------------
Without Flare Gas Recovery
----------------------------------------------------------------------------------------------------------------
PM2.5 Benefits\b\:
SO2.............................. 2,900.................. $190 to $450........... $170 to $410.
NOX.............................. 56..................... $0.36 to $0.87......... $0.32 to $0.78.
PM Total......................... ....................... $190 to $460........... $170 to $410.
CO2 Benefits\c\.................. 110,000\d\............. $2.6................... $2.6.
Total Monetized Benefits..... ....................... $190 to $460........... $170 to $410.
----------------------------------------------------------------------------------------------------------------
\a\ All estimates are for the analysis year (2017) and are rounded to two significant figures so numbers may not
sum across rows. The total monetized benefits reflect the human health benefits associated with reducing
exposure to PM2.5 through reductions of PM2.5 precursors, such as NOX and SO2, as well as CO2. It is important
to note that the monetized benefits do not include reduced health effects from direct exposure to SO2 and NOX,
ozone exposure, ecosystem effects or visibility impairment.
\b\ PM benefits are shown as a range from Pope, et al. (2002) to Laden, et al. (2006). These models assume that
all fine particles, regardless of their chemical composition, are equally potent in causing premature
mortality because the scientific evidence is not yet sufficient to allow differentiation of effects estimates
by particle type.
\c\ The CO2 emission reductions (shown in metric tonnes) have been reduced to reflect the anticipated emission
increases associated with the energy disbenefits. CO2-related benefits were calculated using the social cost
of carbon (SCC), which is discussed further in the RIA. The net present value of reduced CO2 emissions is
calculated differently than other benefits. This table shows monetized climate benefits using the global
average SCC estimate at a 3-percent discount rate because the interagency workgroup deemed the SCC at a 3-
percent discount rate to be the central value. In the RIA, we also provide the monetized CO2 benefits using
discount rates of 5 percent (average), 2.5 percent (average) and 3 percent (95th percentile).
\d\ Metric tonnes
These benefits estimates represent the total monetized human health
benefits for populations exposed to less PM2.5 in 2017 from
controls installed to reduce air pollutants in order to meet this rule.
To estimate human health benefits of this rule, the EPA used benefit-
per-ton factors to quantify the changes in PM2.5-related
health impacts and monetized benefits based on changes in
SO2 and NOX emissions. These benefit-per-ton
factors were derived using the general approach and methodology laid
out in Fann, Fulcher, and Hubbell (2009).\13\ This approach uses a
model to convert emissions of PM2.5 precursors into changes
in ambient PM2.5 levels and another model to estimate the
changes in human health associated with that change in air quality,
which are then divided by the emission reductions to
[[Page 56457]]
create the benefit-per-ton estimates. However, for this rule, we use
air quality modeling data specific to the petroleum refineries
sector.\14\ The primary difference between the estimates used in this
analysis and the estimates reported in Fann, Fulcher, and Hubbell
(2009) is the air quality modeling data utilized. While the air quality
data used in Fann, Fulcher, and Hubbell (2009) reflects broad
pollutant/source category combinations, such as all non-electric
generating unit stationary point sources, the air quality modeling data
used in this analysis is sector-specific. In addition, the updated air
quality modeling data reflects more recent emissions data (2005 rather
than 2001) and has a higher spatial resolution (12 kilometers (km)
rather than 36 km grid cells). As a result, the benefit-per-ton
estimates presented herein better reflect the geographic areas and
populations likely to be affected by this sector. The benefits
methodology, such as health endpoints assessed, risk estimates applied
and valuation techniques applied did not change. However, these updated
estimates still have similar limitations as all national-average
benefit-per-ton estimates in that they reflect the geographic
distribution of the modeled emissions, which may not exactly match the
emission reductions in this rulemaking, and they may not reflect local
variability in population density, meteorology, exposure, baseline
health incidence rates or other local factors for any specific
location.
---------------------------------------------------------------------------
\13\ Fann, N., C.M. Fulcher, B.J. Hubbell. 2009. The Influence
of Location, Source, and Emission Type in Estimates of the Human
Health Benefits of Reducing a Ton of Air Pollution. Air Qual Atmos
Health (2009) 2:169-176.
\14\ U.S. Environmental Protection Agency. 2011. Technical
Support Document: Estimating the Benefit per Ton of Reducing
PM2.5 Precursors from the Petroleum Refineries Sector.
EPA, Research Triangle Park, NC.
---------------------------------------------------------------------------
We apply these national benefit-per-ton estimates calculated for
this sector separately for SO2 and NOX and
multiply them by the corresponding emission reductions. The sector-
specific modeling does not provide estimates of the PM2.5-
related benefits associated with reducing VOC emissions, but these
unquantified benefits are generally small compared to other
PM2.5 precursors. More information regarding the derivation
of the benefit-per-ton estimates for the petroleum refining sector is
available in the technical support document, which is available in the
docket.
These models assume that all fine particles, regardless of their
chemical composition, are equally potent in causing premature mortality
because the scientific evidence is not yet sufficient to allow
differentiation of effects estimates by particle type. The main
PM2.5 precursors affected by this rule are SO2
and NOX. Even though we assume that all fine particles have
equivalent health effects, the benefit-per-ton estimates vary between
precursors depending on the location and magnitude of their impact on
PM2.5 levels, which drive population exposure. For example,
SO2 has a lower benefit-per-ton estimate than direct
PM2.5 because it does not form as much PM2.5,
thus, the exposure would be lower, and the monetized health benefits
would be lower.
It is important to note that the magnitude of the PM2.5
benefits is largely driven by the concentration response function for
premature mortality. Experts have advised the EPA to consider a variety
of assumptions, including estimates based both on empirical
(epidemiological) studies and judgments elicited from scientific
experts, to characterize the uncertainty in the relationship between
PM2.5 concentrations and premature mortality. We cite two
key empirical studies, one based on the American Cancer Society cohort
study \15\ and the extended Six Cities cohort study.\16\ In the RIA for
this final rule, which is available in the docket, we also include
benefits estimates derived from the expert judgments and other
assumptions.
---------------------------------------------------------------------------
\15\ Pope, et al., 2002. Lung Cancer, Cardiopulmonary Mortality,
and Long-term Exposure to Fine Particulate Air Pollution. Journal of
the American Medical Association 287:1132-1141.
\16\ Laden, et al., 2006. Reduction in Fine Particulate Air
Pollution and Mortality. American Journal of Respiratory and
Critical Care Medicine 173: 667-672.
---------------------------------------------------------------------------
The EPA strives to use the best available science to support our
benefits analyses. We recognize that interpretation of the science
regarding air pollution and health is dynamic and evolving. After
reviewing the scientific literature, we have determined that the no-
threshold model is the most appropriate model for assessing the
mortality benefits associated with reducing PM2.5 exposure.
Consistent with this finding, we have conformed the previous threshold
sensitivity analysis to the current state of the PM science by
incorporating a new ``Lowest Measured Level'' (LML) assessment in the
RIA accompanying this rule. While an LML assessment provides some
insight into the level of uncertainty in the estimated PM mortality
benefits, the EPA does not view the LML as a threshold and continues to
quantify PM-related mortality impacts using a full range of modeled air
quality concentrations.
Most of the estimated PM-related benefits in this rule would accrue
to populations exposed to higher levels of PM2.5. For this
analysis, policy-specific air quality data is not available due to time
or resource limitations, thus, we are unable to estimate the percentage
of premature mortality associated with this specific rule's emission
reductions at each PM2.5 level. As a surrogate measure of
mortality impacts, we provide the percentage of the population exposed
at each PM2.5 level using the source apportionment modeling
used to calculate the benefit-per-ton estimates for this sector. Using
the Pope, et al. (2002) study, 77 percent of the population is exposed
to annual mean PM2.5 levels at or above the LML of 7.5
micrograms per cubic meter ([micro]g/m\3\). Using the Laden, et al.
(2006) study, 25 percent of the population is exposed above the LML of
10 [micro]g/m\3\. It is important to emphasize that we have high
confidence in PM2.5-related effects down to the lowest LML
of the major cohort studies. This fact is important, because, as we
model avoided premature deaths among populations exposed to levels of
PM2.5, we have lower confidence in levels below the LML for
each study.
Every benefit analysis examining the potential effects of a change
in environmental protection requirements is limited, to some extent, by
data gaps, model capabilities (such as geographic coverage) and
uncertainties in the underlying scientific and economic studies used to
configure the benefit and cost models. Despite these uncertainties, we
believe the benefit analysis for this rule provides a reasonable
indication of the expected health benefits of the rulemaking under a
set of reasonable assumptions. This analysis does not include the type
of detailed uncertainty assessment found in the 2006 PM2.5
NAAQS RIA because we lack the necessary air quality input and
monitoring data to run the benefits model. In addition, we have not
conducted air quality modeling for this rule, and using a benefit-per-
ton approach adds another important source of uncertainty to the
benefits estimates. The 2006 PM2.5 NAAQS benefits analysis
\17\ provides an indication of the sensitivity of our results to
various assumptions.
---------------------------------------------------------------------------
\17\ U.S. Environmental Protection Agency, 2006. Final
Regulatory Impact Analysis: PM2.5 NAAQS. Prepared by Office of Air
and Radiation. October. Available on the Internet at https://www.epa.gov/ttn/ecas/ria.html.
---------------------------------------------------------------------------
This rule is expected to reduce CO2 emissions from the
electricity sector. The EPA has assigned a dollar value to reductions
in CO2 emissions using recent estimates of the ``social cost
of carbon'' (SCC). The SCC is an estimate
[[Page 56458]]
of the monetized damages associated with an incremental increase in
carbon emissions in a given year or the per metric ton benefit estimate
relating to decreases in CO2 emissions. It is intended to
include (but is not limited to) changes in net agricultural
productivity, human health, property damage from increased flood risk,
and the value of ecosystem services due to climate change.
The SCC estimates used in this analysis were developed through an
interagency process that included the EPA and other executive branch
entities, and that concluded in February 2010. We first used these SCC
estimates in the benefits analysis for the final joint EPA/DOT
Rulemaking to establish Light-Duty Vehicle Greenhouse Gas Emission
Standards and Corporate Average Fuel Economy Standards; see the rule's
preamble for discussion about application of the SCC (75 FR 25324; May
7, 2010). The SCC Technical Support Document (SCC TSD) provides a
complete discussion of the methods used to develop these SCC
estimates.\18\
---------------------------------------------------------------------------
\18\ Docket ID EPA-HQ-OAR-2009-0472-114577, Technical Support
Document: Social Cost of Carbon for Regulatory Impact Analysis Under
Executive Order 12866, Interagency Working Group on Social Cost of
Carbon, with participation by Council of Economic Advisers, Council
on Environmental Quality, Department of Agriculture, Department of
Commerce, Department of Energy, Department of Transportation,
Environmental Protection Agency, National Economic Council, Office
of Energy and Climate Change, Office of Management and Budget,
Office of Science and Technology Policy, and Department of Treasury
(February 2010). Also available at https://epa.gov/otaq/climate/regulations.htm.
---------------------------------------------------------------------------
The interagency group selected four SCC values for use in
regulatory analyses, which we have applied in this analysis: $5.9,
$24.3, $39, and $74.4 per metric ton of CO2 emissions in
2016, in 2007 dollars. The first three values are based on the average
SCC from three integrated assessment models, at discount rates of 5, 3
and 2.5 percent, respectively. Social cost of carbon values at several
discount rates are included because the literature shows that the SCC
is quite sensitive to assumptions about the discount rate, and because
no consensus exists on the appropriate rate to use in an
intergenerational context. The fourth value is the 95th percentile of
the SCC from all three values at a 3-percent discount rate. It is
included to represent higher-than-expected impacts from temperature
change further out in the extremes of the SCC distribution. Low
probability, high impact events are incorporated into all of the SCC
values through explicit consideration of their effects in two of the
three values as well as the use of a probability density function for
equilibrium climate sensitivity. Treating climate sensitivity
probabilistically results in more high temperature outcomes, which in
turn leads to higher projections of damages.
Applying the global SCC estimates using a 3-percent discount rate,
we estimate the value of the climate related benefits of this rule in
2017 is $49 million (2006$), as shown in Table 6. See the RIA for more
detail on the methodology used to calculate these benefits and
additional estimates of climate benefits using different discount rates
and the 95th percentile of the 3-percent discount rate SCC. Important
limitations and uncertainties of the SCC approach are also described in
the RIA.
It should be noted that the monetized benefits estimates provided
above do not include benefits from several important benefit
categories, including direct exposure to SO2 and
NOX, ozone exposure, ecosystem effects and visibility
impairment. Although we do not have sufficient information or modeling
available to provide monetized estimates for this rulemaking, we
include a qualitative assessment of these unquantified benefits in the
RIA for this final rule.
Although this final rule provides refiners with some additional
compliance options and removes some requirements, such as the long-term
H2S limit for flares, these are non-monetized benefits of
the rule.
For more information on the benefits analysis, please refer to the
RIA for this rulemaking, which is available in the docket.
VI. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory Planning and Review and Executive
Order 13563: Improving Regulation and Regulatory Review
Under section 3(f)(1) of Executive Order 12866 (58 FR 51735,
October 4, 1993), this action is an ``economically significant
regulatory action'' because it is likely to have an annual effect on
the economy of $100 million or more. Accordingly, the EPA submitted
this action to the Office of Management and Budget (OMB) for review
under Executive Order 12866 and Executive Order 13563 (76 FR 3821,
January 21, 2011), and any changes made in response to OMB
recommendations have been documented in the docket for this action. In
addition, the EPA prepared a RIA of the potential costs and benefits
associated with this action.
A summary of the monetized benefits, compliance costs and net
benefits for the final rule at discount rates of 3 percent and 7
percent is in Table 7 of this preamble.
Table 7--Summary of the Monetized Benefits, Compliance Costs and Net
Benefits for the Final Petroleum Refineries NSPS in 2017
[Millions of 2006 dollars] \a\
------------------------------------------------------------------------
3-Percent discount 7-Percent discount
rate rate
------------------------------------------------------------------------
Total Monetized Benefits \b\ $270 to $580........ $240 to $530.
Total Compliance Costs \c\.. -$79................ -$79.
Net Benefits................ $340 to $660........ $320 to $610.
-------------------------------------------
Non-Monetized Benefits...... Health effects from direct exposure to SO2
and NO2.
-------------------------------------------
Health effects from PM2.5 exposure from
VOC
-------------------------------------------
Ecosystem effects.
-------------------------------------------
Visibility impairment.
------------------------------------------------------------------------
\a\ All estimates are for the implementation year (2017) and are rounded
to two significant figures.
[[Page 56459]]
\b\ The total monetized benefits reflect the human health benefits
associated with reducing exposure to PM2.5 through reductions of PM2.5
precursors such as NOX and SO2, as well as CO2 benefits. It is
important to note that the monetized benefits do not include the
reduced health effects from direct exposure to SO2 and NOX, ozone
exposure, ecosystem effects or visibility impairment. Human health
benefits are shown as a range from Pope, et al. (2002) to Laden, et
al. (2006). These models assume that all fine particles, regardless of
their chemical composition, are equally potent in causing premature
mortality because the scientific evidence is not yet sufficient to
allow differentiation of effects estimates by particle type. The net
present value of reduced CO2 emissions is calculated differently than
other benefits. This table includes monetized climate benefits using
the global average social cost of carbon (SCC) estimated at a 3-
percent discount rate because the interagency work group deemed the
SCC estimate at a 3-percent discount rate to be the central value.
\c\ The engineering compliance costs are annualized using a 7-percent
discount rate.
To support the determination of BSER for the June 24, 2008, final
rule, we considered a number of regulatory options and their costs and
benefits. Those results are presented in the RIA for the June 24, 2008,
final rulemaking, which is available in the docket. These final rule
amendments are in response to comments received on the December 22,
2008, proposed rule amendments. Costs and benefits associated with the
amendments in this final rule differ from the June 24, 2008, final rule
and the December 22, 2008, proposed rule amendments primarily as a
result of correcting the number of flares projected to have to comply
with this rule (i.e., 400 affected flares in this rule compared to 40
estimated in the June 24, 2008, final rule and 150 in the December 22,
2008, proposed amendments). In addition, the amendments in this final
rule to address comments received for the other fuel gas combustion
devices do not affect the projected costs and benefits from the
December 22, 2008, proposal, which also did not change from the June
24, 2008, final rule. Therefore, for purposes of developing these final
rule amendments, we did not re-evaluate the suite of regulatory options
for flares and other fuel gas combustion devices considered to support
the June 24, 2008, final rule. However, even with the flare count
adjustment, this final rule is consistent with Executive Order 13563
(Improving Regulation and Regulatory Review) because the monetized
benefits of this final rule exceed the costs. In addition, for
facilities implementing flare gas recovery, we are reducing regulatory
burden by finalizing provisions that would allow the owner or operator
to reduce monitoring costs and the number of root cause analyses,
corrective actions and corresponding recordkeeping and reporting they
would need to perform.
For more information on the cost-benefits analysis, please refer to
the RIA for this rulemaking, which is available in the docket.
B. Paperwork Reduction Act
The final amendments to the Standards of Performance for Petroleum
Refineries (40 CFR part 60, subpart J) do not impose any new
information collection burden. The final amendments are clarifications
and technical corrections that do not affect the estimated burden of
the existing rule. Therefore, we have not revised the ICR for the
existing rule. However, OMB has previously approved the information
collection requirements contained in the existing rule (40 CFR part 60,
subpart J) under the provisions of the Paperwork Reduction Act, 44
U.S.C. 3501, et seq., and has assigned OMB control number 2060-0022.
The OMB control numbers for the EPA's regulations are listed in 40 CFR
part 9.
The OMB has approved the information collection requirements in the
amendments to the Standards of Performance for Petroleum Refineries for
Which Construction, Reconstruction, or Modification Commenced After May
14, 2007 (40 CFR part 60, subpart Ja) under the provisions of the
Paperwork Reduction Act, 44 U.S.C. 3501, et seq., and has assigned OMB
control number 2060-0602.
The information requirements in these final amendments add new
compliance options, provide more time to comply with the requirements
for flares, clarify the flare management plan requirements and clarify
the flare modification provision. Overall, these changes are expected
to reduce the costs associated with testing, monitoring, recording and
reporting, so they will not result in any increase in burden for the
affected facilities for which the EPA previously estimated the burden.
However, the EPA has revised the number of flares expected to become
subject to the rule over the first 3 years of the ICR. Therefore, the
annual burden was estimated for the additional affected facilities. The
total burden for 40 CFR part 60, subpart Ja can be estimated by summing
the previously approved annual burden for OMB control number 2060-0602
(5,340 labor-hours per year at a cost of $481,249 per year, annualized
capital costs of $2,052,000 per year, and operation and maintenance
costs of $1,117,440 per year) and the annual burden for this ICR, as
described below.
The annual burden for this information collection averaged over the
first 3 years of this ICR is estimated to total 54,572 labor-hours per
year at a cost of $4,918,110 per year. The annualized capital costs are
estimated at $11,266,000 per year and operation and maintenance costs
are estimated at $8,750,000 per year. We note that the capital costs,
as well as the operation and maintenance costs, are for the continuous
monitors; these costs are also included in the cost impacts presented
in section V.A of this preamble. Therefore, the burden costs associated
with the continuous monitors presented in the ICR are not additional
costs incurred by affected sources subject to final 40 CFR part 60,
subpart Ja. Burden is defined at 5 CFR 1320.3(b).
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 are listed in 40 CFR part 9. The EPA is amending the
table in 40 CFR part 9 of currently approved ICR control numbers for
various regulations to list regulatory citations for the information
requirements contained in this final rule. This amendment updates the
table to list the information collection requirements being promulgated
here as amendments to the NSPS for petroleum refineries.
The EPA will continue to present OMB control numbers in a
consolidated table format to be codified in 40 CFR part 9 of the
agency's regulations and in each CFR volume containing the EPA
regulations. The table lists the section numbers with reporting and
recordkeeping requirements and the current OMB control numbers. This
listing of the OMB control numbers and their subsequent codification in
the CFR satisfy the requirements of the Paperwork Reduction Act (44
U.S.C. 3501, et seq.) and OMB's implementing regulations at 5 CFR part
1320.
C. Regulatory Flexibility Act
The Regulatory Flexibility Act generally requires an agency to
prepare a regulatory flexibility analysis of any rule subject to notice
and comment rulemaking requirements under the Administrative Procedure
Act or any other statute unless the agency certifies that the rule
would not have a significant economic impact on a substantial number of
small entities. Small entities include small businesses, small
organizations and small governmental jurisdictions.
[[Page 56460]]
For purposes of assessing the impact of this final action on small
entities, small entity is defined as: (1) A small business whose parent
company has no more than 1,500 employees, that is primarily engaged in
refining crude petroleum into refined petroleum as defined by NAICS
code 32411 (as defined by Small Business Administration size
standards); (2) a small governmental jurisdiction that is a government
of a city, county, town, school district or special district with a
population of less than 50,000; and (3) a small organization that is
any not-for-profit enterprise which is independently owned and operated
and is not dominant in its field.
While we estimated the natural gas recovery offsets or credit at a
national level and believe that larger firms are more likely to offset
natural gas purchases, the revenues from natural gas recovery offsets
might mask disproportionate impacts on small refiners. To better
identify disproportionate impacts, we examined the potential impacts on
refiners based on a scenario where no firms adopt flare gas recovery
systems and comply with the NSPS through flare monitoring and flare
management and root cause analysis actions. The incremental compliance
costs imposed on small refineries are not estimated to create
significant impacts on a cost-to-sales ratio basis at the firm level.
Therefore, no adverse economic impacts are expected for any small or
large entity.
After considering the economic impacts of these final amendments on
small entities, I certify that this action will not have a significant
economic impact on a substantial number of small entities. The small
entities directly regulated by these final amendments are small
petroleum refineries. We have determined that 31 small refiners, or 55
percent of total refiners, will experience an impact of between less
than 0.01 percent up to 0.63 percent of revenues.
D. Unfunded Mandates Reform Act
This rule does not contain a federal mandate that may result in
expenditures of $100 million or more for state, local and tribal
governments, in the aggregate, or the private sector in any one year.
The costs of the final amendments would not increase costs associated
with the final rule. Thus, this rule is not subject to the requirements
of sections 202 or 205 of the UMRA.
This rule is also not subject to the requirements of section 203 of
UMRA because it contains no regulatory requirements that might
significantly or uniquely affect small governments. The final
amendments contain no requirements that apply to such governments and
impose no obligations upon them.
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, as
specified in Executive Order 13132. This action does not modify
existing responsibilities or create new responsibilities among EPA
Regional offices, states or local enforcement agencies. Thus, Executive
Order 13132 does not apply to this action.
F. Executive Order 13175: Consultation and Coordination With Indian
Tribal Governments
This action does not have tribal implications, as specified in
Executive Order 13175 (65 FR 67249, November 9, 2000). The final
amendments impose no requirements on tribal governments. Thus,
Executive Order 13175 does not apply to this action.
G. Executive Order 13045: Protection of Children From Environmental
Health Risks and Safety Risks
The EPA interprets Executive Order 13045 (62 FR 19885, April 23,
1997) as applying to those regulatory actions that concern health or
safety risks, such that the analysis required under section 5-501 of
the Executive Order has the potential to influence the regulation. This
action is not subject to Executive Order 13045 because it is based
solely on technology performance.
H. Executive Order 13211: Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution, or Use
This action is not a ``significant energy action'' as defined in
Executive Order 13211 (66 FR 28355, May 22, 2001), because it is not
likely to have a significant adverse effect on the supply, distribution
or use of energy. The final amendments would not increase the level of
energy consumption required for the final rule and may decrease energy
requirements.
I. National Technology Transfer and Advancement Act
Section 12(d) of the National Technology Transfer and Advancement
Act of 1995 (NTTAA), Public Law 104-113, 12(d) (15 U.S.C. 272 note)
directs the EPA to use voluntary consensus standards (VCS) in its
regulatory activities, unless to do so would be inconsistent with
applicable law or otherwise impractical. VCS are technical standards
(e.g., materials specifications, test methods, sampling procedures and
business practices) that are developed or adopted by VCS bodies. NTTAA
directs the EPA to provide Congress, through OMB, explanations when the
agency decides not to use available and applicable VCS.
This rulemaking involves technical standards. The EPA has decided
to use the following VCS for determining the higher heating value of
fuel fed to process heaters: ASTM D240-02 (Reapproved 2007), Standard
Test Method for Heat of Combustion of Liquid Hydrocarbon Fuels by Bomb
Calorimeter; ASTM D1826-94 (Reapproved 2003), Standard Test Method for
Calorific (Heating) Value of Gases in Natural Gas Range by Continuous
Recording Calorimeter; ASTM D3588-98 (Reapproved 2003), Standard
Practice for Calculating Heat Value, Compressibility Factor, and
Relative Density of Gaseous Fuels; ASTM D4809-06, Standard Test Method
for Heat of Combustion of Liquid Hydrocarbon Fuels by Bomb Calorimeter
(Precision Method); ASTM D4891-89 (Reapproved 2006), Standard Test
Method for Heating Value of Gases in Natural Gas Range by
Stoichiometric Combustion; ASTM D1945-03 (Reapproved 2010), Standard
Method for Analysis of Natural Gas by Gas Chromatography; and ASTM
D1946-90 (Reapproved 2006), Standard Method for Analysis of Reformed
Gas by Gas Chromatography.
The EPA has decided to use the following VCS as acceptable
alternatives to EPA Methods 2, 2A, 2B, 2C or 2D for conducting relative
accuracy evaluations of fuel gas flow monitors: American Society of
Mechanical Engineers (ASME) MFC-3M-2004, Measurement of Fluid Flow in
Pipes Using Orifice, Nozzle, and Venturi; ANSI/ASME MFC-4M-1986
(Reaffirmed 2008), Measurement of Gas Flow by Turbine Meters; ASME MFC-
6M-1998 (Reaffirmed 2005), Measurement of Fluid Flow in Pipes Using
Vortex Flowmeters; ASME/ANSI MFC-7M-1987 (Reaffirmed 2006), Measurement
of Gas Flow by Means of Critical Flow Venturi Nozzles; ASME MFC-11M-
2006, Measurement of Fluid Flow by Means of Coriolis Mass Flowmeters;
ASME MFC-14M-2003, Measurement of Fluid Flow Using Small Bore Precision
Orifice Meters; and ASME MFC-18M-2001, Measurement of Fluid Flow Using
Variable Area Meters.
[[Page 56461]]
The EPA has also decided to use the following VCS as acceptable
alternatives to EPA Methods 2, 2A, 2B, 2C or 2D for conducting relative
accuracy evaluations of fuel oil flow monitors: ANSI/ASME MFC-5M-1985
(Reaffirmed 2006), Measurement of Liquid Flow in Closed Conduits Using
Transit-Time Ultrasonic Flowmeters; ASME/ANSI MFC-9M-1988 (Reaffirmed
2006), Measurement of Liquid Flow in Closed Conduits by Weighing
Method; ASME MFC-16-2007, Measurement of Liquid Flow in Closed Conduits
with Electromagnetic Flowmeters; ASME MFC-22-2007, Measurement of
Liquid by Turbine Flowmeters; and ISO 8316: Measurement of Liquid Flow
in Closed Conduits--Method by Collection of the Liquid in a Volumetric
Tank (1987-10-01)--First Edition.
The EPA has decided to use the following VCS as acceptable
alternatives to EPA Method 15A and 16A for conducting relative accuracy
evaluations of monitors for reduced sulfur compounds, total sulfur
compounds, and H2S: ANSI/ASME PTC 19.10-1981, Flue and
Exhaust Gas Analyses. The EPA has decided to use the following VCS as
acceptable alternatives to EPA Method 16A for analysis of total sulfur
samples: ASTM D4468-85 (Reapproved 2006), Standard Test Method for
Total Sulfur in Gaseous Fuels by Hydrogenolysis and Rateometric
Colorimetry; and ASTM D5504-08, Standard Test Method for Determination
of Sulfur Compounds in Natural Gas and Gaseous Fuels by Gas
Chromatography and Chemiluminescence.
The EPA has decided to use the following VCS as acceptable
alternatives to EPA Method 18 for relative accuracy evaluations of gas
composition analyzers for gas-fired process heaters: ASTM D1945-03
(Reapproved 2010), Standard Method for Analysis of Natural Gas by Gas
Chromatography; ASTM D1946-90 (Reapproved 2006), Standard Method for
Analysis of Reformed Gas by Gas Chromatography; ASTM UOP539-97,
Refinery Gas Analysis by Gas Chromatography; and ASTM D6420-99
(Reapproved 2004), Standard Test Method for Determination of Gaseous
Organic Compounds by Direct Interface Gas Chromatography-Mass
Spectrometry. However, ASTM D6420-99 is a suitable alternative to EPA
Method 18 only where:
(1) The target compound(s) are those listed in Section 1.1 of ASTM
D6420-99, and
(2) The target concentration is between 150 parts per billion by
volume and 100 ppmv.
For target compound(s) not listed in Section 1.1 of ASTM D6420-99,
but potentially detected by mass spectrometry, the regulation specifies
that the additional system continuing calibration check after each run,
as detailed in Section 10.5.3 of the ASTM method, must be followed,
met, documented and submitted with the data report even if there is no
moisture condenser used or the compound is not considered water
soluble. For target compound(s) not listed in Section 1.1 of ASTM
D6420-99 and not amenable to detection by mass spectrometry, ASTM
D6420-99 does not apply.
These above-listed VCS are incorporated by reference (see 40 CFR
60.17).
The EPA has also decided to use American Gas Association Report No.
3: Orifice Metering for Natural Gas and Other Related Hydrocarbon
Fluids, Part 1: General Equations and Uncertainty Guidelines (1990),
American Gas Association Report No. 3: Orifice Metering for Natural Gas
and Other Related Hydrocarbon Fluids, Part 2: Specification and
Installation Requirements (2000), American Gas Association Report No.
11: Measurement of Natural Gas by Coriolis Meter (2003), American Gas
Association Transmission Measurement Committee Report No. 7,
Measurement of Natural Gas by Turbine Meters (Revised February 2006)
and API's Manual of Petroleum Measurement Standards, Chapter 22--
Testing Protocol, Section 2--Differential Pressure Flow Measurement
Devices, First Edition, August 2005, for conducting relative accuracy
evaluations of fuel gas flow monitors; Gas Processors Association (GPA)
Standard 2261-00, Analysis for Natural Gas and Similar Gaseous Mixtures
by Gas Chromatography (2000), for relative accuracy evaluations of gas
composition analyzers for gas-fired process heaters; and GPA 2172-09,
Calculation of Gross Heating Value, Relative Density, Compressibility
and Theoretical Hydrocarbon Liquid Content for Natural Gas Mixtures for
Custody Transfer, for determining the higher heating value of fuel fed
to process heaters. These methods are also incorporated by reference
(see 40 CFR 60.17).
While the agency has identified five VCS as being potentially
applicable to this rule, we have decided not to use these VCS in this
rulemaking. The use of these VCS would be impractical because they do
not meet the objectives of the standards cited in this rule. See the
docket for this rule for the reasons for these determinations.
Under 40 CFR 60.13(i) of the NSPS General Provisions, a source may
apply to the EPA for permission to use alternative test methods or
alternative monitoring requirements in place of any required testing
methods, performance specifications or procedures in the final rule and
amendments.
J. Executive Order 12898: Federal Actions To Address Environmental
Justice in Minority Populations and Low-Income Populations
Executive Order 12898 (59 FR 7629, February 16, 1994) establishes
federal executive policy on environmental justice. Its main provision
directs federal agencies, to the greatest extent practicable and
permitted by law, to make environmental justice part of their mission
by identifying and addressing, as appropriate, disproportionately high
and adverse human health or environmental effects of their programs,
policies and activities on minority populations and low-income
populations in the United States.
The EPA has determined that this final rule will not have
disproportionately high and adverse human health or environmental
effects on minority or low-income populations because it does not
affect the level of protection provided to human health or the
environment. The final amendments are either clarifications or
compliance alternatives which will neither increase or decrease
environmental protection.
K. Congressional Review Act
The Congressional Review Act, 5 U.S.C. 801, et seq., as added by
the Small Business Regulatory Enforcement Fairness Act of 1996,
generally provides that before a rule may take effect the agency
promulgating the rule must submit a rule report, which includes a copy
of the rule, to each House of Congress and to the Comptroller General
of the United States. The EPA will submit a report containing these
final rules and other required information to the United States Senate,
the United States House of Representatives and the Comptroller General
of the United States prior to publication of the final rules in the
Federal Register. A major rule cannot take effect until 60 days after
it is published in the Federal Register. This action is a ``major
rule'' as defined by 5 U.S.C. 804(2). This final rule will be effective
on November 13, 2012.
[[Page 56462]]
List of Subjects
40 CFR Part 9
Environmental protection, Reporting and recordkeeping requirements.
40 CFR Part 60
Environmental protection, Administrative practice and procedure,
Air pollution control, Incorporation by reference, Intergovernmental
relations, Reporting and recordkeeping requirements.
Dated: June 1, 2012.
Lisa P. Jackson,
Administrator.
For the reasons stated in the preamble, title 40, chapter I, of the
Code of Federal Regulations is amended as follows:
PART 9--[AMENDED]
0
1. The authority citation for part 9 continues to read as follows:
Authority: 7 U.S.C. 135, et seq., 136-136y; 15 U.S.C. 2001,
2003, 2005, 2006, 2601-2671; 21 U.S.C. 331j, 346a, 348; 31 U.S.C.
9701; 33 U.S.C. 1251, et seq., 1311, 1313d, 1314, 1318, 1321, 1326,
1330, 1342, 1344, 1345(d) and (e), 1361; E.O. 11735, 38 FR 21243, 3
CFR, 1971-1975 Comp. p. 973; 42 U.S.C. 241, 242b, 243, 246, 300f,
300g, 300g-1, 300g-2, 300g-3, 300g-4, 300g-5, 300g-6, 300j-1, 300j-
2, 300j-3, 300j-4, 300j-9, 1857, et seq., 6901-6992k, 7401-7671q,
7542, 9601-9657, 11023, 11048.
0
2. The table in Section 9.1 is amended by adding an entry in numerical
order for 60.103a-60.108a under the heading ``Standards of Performance
for New Stationary Sources'' to read as follows:
Sec. 9.1 OMB Approvals under the Paperwork Reduction Act.
* * * * *
------------------------------------------------------------------------
OMB control
40 CFR citation No.
------------------------------------------------------------------------
* * * * *
------------------------------------------------------------------------
Standards of Performance for New Stationary Sources \1\
------------------------------------------------------------------------
* * * * *
------------------------------------------------------------------------
60.103a-60.108a......................................... 2060-0602
* * * * *
------------------------------------------------------------------------
\1\ The ICRs referenced in this section of the table encompass the
applicable general provisions contained in 40 CFR part 60, subpart A,
which are not independent information collection requirements.
* * * * *
PART 60--[AMENDED]
0
3. The authority citation for part 60 continues to read as follows:
Authority: 42 U.S.C. 7401, et seq.
Subpart A--[AMENDED]
0
4. Section 60.17 is amended by:
0
a. Revising paragraphs (a)(84), (a)(95), (a)(96), (a)(97), and (a)(98);
0
b. Adding paragraphs (a)(100) through (a)(108);
0
c. Adding paragraph (c)(2);
0
d. Revising paragraph (h)(4) and adding paragraphs (h)(5) through
(h)(15);
0
e. Adding paragraphs (m)(2) and (m)(3); and
0
f. Adding paragraphs (p) and (q) to read as follows:
Sec. 60.17 Incorporations by reference.
* * * * *
(a) * * *
(84) ASTM D6420-99 (Reapproved 2004), Standard Test Method for
Determination of Gaseous Organic Compounds by Direct Interface Gas
Chromatography-Mass Spectrometry, (Approved October 1, 2004), IBR
approved for Sec. 60.107a(d) of subpart Ja and table 2 of subpart JJJJ
of this part.
* * * * *
(95) ASTM D3588-98 (Reapproved 2003), Standard Practice for
Calculating Heat Value, Compressibility Factor, and Relative Density of
Gaseous Fuels, (Approved May 10, 2003), IBR approved for Sec. Sec.
60.107a(d) and 60.5413(d).
(96) ASTM D4891-89 (Reapproved 2006), Standard Test Method for
Heating Value of Gases in Natural Gas Range by Stoichiometric
Combustion, (Approved June 1, 2006), IBR approved for Sec. Sec.
60.107a(d) and 60.5413(d).
(97) ASTM D1945-03 (Reapproved 2010), Standard Method for Analysis
of Natural Gas by Gas Chromatography, (Approved January 1, 2010), IBR
approved for Sec. Sec. 60.107a(d) and 60.5413(d).
(98) ASTM D5504-08, Standard Test Method for Determination of
Sulfur Compounds in Natural Gas and Gaseous Fuels by Gas Chromatography
and Chemiluminescence, (Approved June 15, 2008), IBR approved for
Sec. Sec. 60.107a(e) and 60.5413(d).
* * * * *
(100) ASTM D4468-85 (Reapproved 2006), Standard Test Method for
Total Sulfur in Gaseous Fuels by Hydrogenolysis and Rateometric
Colorimetry (Approved June 1, 2006), IBR approved for Sec. 60.107a(e).
(101) ASTM D240-02 (Reapproved 2007), Standard Test Method for Heat
of Combustion of Liquid Hydrocarbon Fuels by Bomb Calorimeter,
(Approved May 1, 2007), IBR approved for Sec. 60.107a(d).
(102) ASTM D1826-94 (Reapproved 2003), Standard Test Method for
Calorific (Heating) Value of Gases in Natural Gas Range by Continuous
Recording Calorimeter, (Approved May 10, 2003), IBR approved for Sec.
60.107a(d).
(103) ASTM D1946-90 (Reapproved 2006), Standard Method for Analysis
of Reformed Gas by Gas Chromatography, (Approved June 1, 2006), IBR
approved for Sec. 60.107a(d).
(104) ASTM D4809-06, Standard Test Method for Heat of Combustion of
Liquid Hydrocarbon Fuels by Bomb Calorimeter (Precision Method),
(Approved December 1, 2006), IBR approved for Sec. 60.107a(d).
(105) ASTM UOP539-97, Refinery Gas Analysis by Gas Chromatography,
(Copyright 1997), IBR approved for Sec. 60.107a(d).
(106) ASTM D3699-08, Standard Specification for Kerosine, including
Appendix X1, (Approved September 1, 2008), IBR approved for Sec. Sec.
60.41b of subpart Db and 60.41c of subpart Dc of this part.
(107) ASTM D6751-11b, Standard Specification for Biodiesel Fuel
Blend Stock (B100) for Middle Distillate Fuels, including Appendices X1
through X3, (Approved July 15, 2011), IBR approved for Sec. Sec.
60.41b of subpart Db and 60.41c of subpart Dc of this part.
(108) ASTM D7467-10, Standard Specification for Diesel Fuel Oil,
Biodiesel Blend (B6 to B20), including Appendices X1 through X3,
(Approved August 1, 2010), IBR approved for Sec. Sec. 60.41b of
subpart Db and 60.41c of subpart Dc of this part.
* * * * *
(c) * * *
(2) American Petroleum Institute (API) Manual of Petroleum
Measurement Standards, Chapter 22-Testing Protocol, Section 2-
Differential Pressure Flow Measurement Devices, First Edition, August
2005, IBR approved for Sec. 60.107a(d) of subpart Ja of this part.
* * * * *
(h) * * *
(4) ANSI/ASME PTC 19.10-1981, Flue and Exhaust Gas Analyses [Part
10, Instruments and Apparatus], (Issued August 31, 1981), IBR approved
for Sec. 60.56c(b), Sec. 60.63(f), Sec. 60.106(e), Sec. 60.104a(d),
(h), (i), and (j), Sec. 60.105a(d), (f), and (g), Sec. 60.106a(a),
Sec. 60.107a(a), (c), and (e), tables 1 and 3 of subpart EEEE, tables
2 and 4 of subpart FFFF, table 2 of subpart JJJJ, Sec. Sec.
60.4415(a), 60.2145(s), 60.2145(t),
[[Page 56463]]
60.2710(s), 60.2710(t), 60.2710(w), 60.2730(q), 60.4900(b), 60.5220(b),
tables 1 and 2 to subpart LLLL, tables 2 and 3 to subpart MMMM,
Sec. Sec. 60.5406(c) and 60.5413(b).
(5) ASME MFC-3M-2004, Measurement of Fluid Flow in Pipes Using
Orifice, Nozzle, and Venturi, IBR approved for Sec. 60.107a(d) of
subpart Ja of this part.
(6) ANSI/ASME MFC-4M-1986 (Reaffirmed 2008), Measurement of Gas
Flow by Turbine Meters, IBR approved for Sec. 60.107a(d) of subpart Ja
of this part.
(7) ANSI/ASME-MFC-5M-1985 (Reaffirmed 2006), Measurement of Liquid
Flow in Closed Conduits Using Transit-Time Ultrasonic Flowmeters, IBR
approved for Sec. 60.107a(d) of subpart Ja of this part.
(8) ASME MFC-6M-1998 (Reaffirmed 2005), Measurement of Fluid Flow
in Pipes Using Vortex Flowmeters, IBR approved for Sec. 60.107a(d) of
subpart Ja of this part.
(9) ASME/ANSI MFC-7M-1987 (Reaffirmed 2006), Measurement of Gas
Flow by Means of Critical Flow Venturi Nozzles, IBR approved for Sec.
60.107a(d) of subpart Ja of this part.
(10) ASME/ANSI MFC-9M-1988 (Reaffirmed 2006), Measurement of Liquid
Flow in Closed Conduits by Weighing Method, IBR approved for Sec.
60.107a(d) of subpart Ja of this part.
(11) ASME MFC-11M-2006, Measurement of Fluid Flow by Means of
Coriolis Mass Flowmeters, IBR approved for Sec. 60.107a(d) of subpart
Ja of this part.
(12) ASME MFC-14M-2003, Measurement of Fluid Flow Using Small Bore
Precision Orifice Meters, IBR approved for Sec. 60.107a(d) of subpart
Ja of this part.
(13) ASME MFC-16-2007, Measurement of Liquid Flow in Closed
Conduits with Electromagnetic Flowmeters, IBR approved for Sec.
60.107a(d) of subpart Ja of this part.
(14) ASME MFC-18M-2001, Measurement of Fluid Flow Using Variable
Area Meters, IBR approved for Sec. 60.107a(d) of subpart Ja of this
part.
(15) ASME MFC-22-2007, Measurement of Liquid by Turbine Flowmeters,
IBR approved for Sec. 60.107a(d) of subpart Ja of this part.
* * * * *
(m) * * *
(2) Gas Processors Association Standard 2172-09, Calculation of
Gross Heating Value, Relative Density, Compressibility and Theoretical
Hydrocarbon Liquid Content for Natural Gas Mixtures for Custody
Transfer (2009), IBR approved for Sec. 60.107a(d) of subpart Ja of
this part.
(3) Gas Processors Association Standard 2261-00, Analysis for
Natural Gas and Similar Gaseous Mixtures by Gas Chromatography (2000),
IBR approved for Sec. 60.107a(d) of subpart Ja of this part.
* * * * *
(p) The following American Gas Association material is available
for purchase from the following address: ILI Infodisk, 610 Winters
Avenue, Paramus, New Jersey 07652:
(1) American Gas Association Report No. 3: Orifice Metering for
Natural Gas and Other Related Hydrocarbon Fluids, Part 1: General
Equations and Uncertainty Guidelines (1990), IBR approved for Sec.
60.107a(d) of subpart Ja of this part.
(2) American Gas Association Report No. 3: Orifice Metering for
Natural Gas and Other Related Hydrocarbon Fluids, Part 2: Specification
and Installation Requirements (2000), IBR approved for Sec. 60.107a(d)
of subpart Ja of this part.
(3) American Gas Association Report No. 11: Measurement of Natural
Gas by Coriolis Meter (2003), IBR approved for Sec. 60.107a(d) of
subpart Ja of this part.
(4) American Gas Association Transmission Measurement Committee
Report No. 7: Measurement of Gas by Turbine Meters (Revised February
2006), IBR approved for Sec. 60.107a(d) of subpart Ja of this part.
(q) The following material is available for purchase from the
International Standards Organization (ISO), 1, ch. de la Voie-Creuse,
Case postale 56, CH-1211 Geneva 20, Switzerland, +41 22 749 01 11,
https://www.iso.org/iso/home.htm.
(1) ISO 8316: Measurement of Liquid Flow in Closed Conduits--Method
by Collection of the Liquid in a Volumetric Tank (1987-10-01)--First
Edition, IBR approved for Sec. 60.107a(d) of subpart Ja of this part.
(2) [Reserved]
Subpart J--[AMENDED]
0
5. Section 60.100 is amended by:
0
a. Revising paragraph (b);
0
b. Redesignating paragraph (e) as (f); and
0
c. Adding a new paragraph (e) to read as follows:
Sec. 60.100 Applicability, designation of affected facility, and
reconstruction.
* * * * *
(b) Any fluid catalytic cracking unit catalyst regenerator or fuel
gas combustion device under paragraph (a) of this section other than a
flare which commences construction, reconstruction or modification
after June 11, 1973, and on or before May 14, 2007, or any fuel gas
combustion device under paragraph (a) of this section that is also a
flare which commences construction, reconstruction or modification
after June 11, 1973, and on or before June 24, 2008, or any Claus
sulfur recovery plant under paragraph (a) of this section which
commences construction, reconstruction or modification after October 4,
1976, and on or before May 14, 2007, is subject to the requirements of
this subpart except as provided under paragraphs (c) through (e) of
this section.
* * * * *
(e) Owners or operators may choose to comply with the applicable
provisions of subpart Ja of this part to satisfy the requirements of
this subpart for an affected facility.
* * * * *
0
6. Section 60.101 is amended by revising paragraph (d) to read as
follows:
Sec. 60.101 Definitions.
* * * * *
(d) Fuel gas means any gas which is generated at a petroleum
refinery and which is combusted. Fuel gas includes natural gas when the
natural gas is combined and combusted in any proportion with a gas
generated at a refinery. Fuel gas does not include gases generated by
catalytic cracking unit catalyst regenerators and fluid coking burners.
Fuel gas does not include vapors that are collected and combusted in a
thermal oxidizer or flare installed to control emissions from
wastewater treatment units or marine tank vessel loading operations.
* * * * *
0
7. Section 60.106 is amended by revising paragraph (c)(1) to read as
follows:
Sec. 60.106 Test methods and procedures.
* * * * *
(c) * * *
(1) The allowable emission rate (Es) of PM shall be
computed for each run using the following equation:
Es = F + A (H/Rc)
Where:
Es = Emission rate of PM allowed, kg/Mg (lb/ton) of coke
burn-off in catalyst regenerator.
F = Emission standard, 1.0 kg/Mg (2.0 lb/ton) of coke burn-off in
catalyst regenerator.
A = Allowable incremental rate of PM emissions, 43 g/GJ (0.10 lb/
million Btu).
H = Heat input rate from solid or liquid fossil fuel, GJ/hr (million
Btu/hr).
Rc = Coke burn-off rate, Mg coke/hr (ton coke/hr).
* * * * *
[[Page 56464]]
Subpart Ja--[AMENDED]
0
7. In Sec. 60.100a, lift the stay on paragraph (c) published December
22, 2008 (73 FR 78552).
0
8. Section 60.100a is amended by:
0
a. Revising paragraph (a);
0
b. Revising paragraph (b);
0
c. Revising paragraph (c) introductory text and paragraph (c)(1); and
0
d. Revising paragraph (d).
The revisions read as follows:
Sec. 60.100a Applicability, designation of affected facility, and
reconstruction.
(a) The provisions of this subpart apply to the following affected
facilities in petroleum refineries: fluid catalytic cracking units
(FCCU), fluid coking units (FCU), delayed coking units, fuel gas
combustion devices (including process heaters), flares and sulfur
recovery plants. The sulfur recovery plant need not be physically
located within the boundaries of a petroleum refinery to be an affected
facility, provided it processes gases produced within a petroleum
refinery.
(b) Except for flares and delayed coking units, the provisions of
this subpart apply only to affected facilities under paragraph (a) of
this section which commence construction, modification or
reconstruction after May 14, 2007. For flares, the provisions of this
subpart apply only to flares which commence construction, modification
or reconstruction after June 24, 2008. For the purposes of this
subpart, a modification to a flare commences when a project that
includes any of the activities in paragraphs (c)(1) or (2) of this
section is commenced. For delayed coking units, the provisions of this
subpart apply to delayed coking units that commence construction,
reconstruction or modification on the earliest of the following dates:
(1) May 14, 2007, for such activities that involve a ``delayed
coking unit'' defined as follows: one or more refinery process units in
which high molecular weight petroleum derivatives are thermally cracked
and petroleum coke is produced in a series of closed, batch system
reactors;
(2) December 22, 2008, for such activities that involve a ``delayed
coking unit'' defined as follows: a refinery process unit in which high
molecular weight petroleum derivatives are thermally cracked and
petroleum coke is produced in a series of closed, batch system
reactors. A delayed coking unit consists of the coke drums and
associated fractionator;
(3) September 12, 2012, for such activities that involve a
``delayed coking unit'' as defined in Sec. 60.101a.
(c) For all affected facilities other than flares, the provisions
in Sec. 60.14 regarding modification apply. As provided in Sec.
60.14(f), the special provisions set forth under this subpart shall
supersede the provisions in Sec. 60.14 with respect to flares. For the
purposes of this subpart, a modification to a flare occurs as provided
in paragraphs (c)(1) or (2) of this section.
(1) Any new piping from a refinery process unit, including
ancillary equipment, or a fuel gas system is physically connected to
the flare (e.g., for direct emergency relief or some form of continuous
or intermittent venting). However, the connections described in
paragraphs (c)(1)(i) through (vii) of this section are not considered
modifications of a flare.
(i) Connections made to install monitoring systems to the flare.
(ii) Connections made to install a flare gas recovery system or
connections made to upgrade or enhance components of a flare gas
recovery system (e.g., addition of compressors or recycle lines).
(iii) Connections made to replace or upgrade existing pressure
relief or safety valves, provided the new pressure relief or safety
valve has a set point opening pressure no lower and an internal
diameter no greater than the existing equipment being replaced or
upgraded.
(iv) Connections made for flare gas sulfur removal.
(v) Connections made to install back-up (redundant) equipment
associated with the flare (such as a back-up compressor) that does not
increase the capacity of the flare.
(vi) Replacing piping or moving an existing connection from a
refinery process unit to a new location in the same flare, provided the
new pipe diameter is less than or equal to the diameter of the pipe/
connection being replaced/moved.
(vii) Connections that interconnect two or more flares.
* * * * *
(d) For purposes of this subpart, under Sec. 60.15, the ``fixed
capital cost of the new components'' includes the fixed capital cost of
all depreciable components which are or will be replaced pursuant to
all continuous programs of component replacement which are commenced
within any 2-year period following the relevant applicability date
specified in paragraph (b) of this section.
0
9. In Sec. 60.101a, lift the stay on the definition of ``flare''
published December 22, 2008 (73 FR 78552).
0
10. Section 60.101a is amended by:
0
a. Revising the introductory text;
0
b. Adding, in alphabetical order, definitions of ``Air preheat,''
``Ancillary equipment,'' ``Cascaded flare system,'' ``Co-fired process
heater,'' ``Corrective action,'' ``Corrective action analysis,''
``Emergency flare,'' ``Flare gas header system,'' ``Flare gas recovery
system,'' ``Forced draft process heater,'' ``Natural draft process
heater,'' ``Non-emergency flare,'' ``Primary flare,'' ``Purge gas,''
``Root cause analysis,'' ``Secondary flare,'' and ``Sweep gas''; and
0
c. Revising the definitions of ``Delayed coking unit,'' ``Flare,''
``Flexicoking unit,'' ``Fluid coking unit,'' ``Fuel gas,'' ``Fuel gas
combustion device,'' ``Petroleum refinery,'' ``Process upset gas'' and
``Sulfur recovery plant''
The revisions and additions read as follows:
Sec. 60.101a Definitions.
Terms used in this subpart are defined in the Clean Air Act (CAA),
in Sec. 60.2 and in this section.
Air preheat means a device used to heat the air supplied to a
process heater generally by use of a heat exchanger to recover the
sensible heat of exhaust gas from the process heater.
Ancillary equipment means equipment used in conjunction with or
that serve a refinery process unit. Ancillary equipment includes, but
is not limited to, storage tanks, product loading operations,
wastewater treatment systems, steam- or electricity-producing units
(including coke gasification units), pressure relief valves, pumps,
sampling vents and continuous analyzer vents.
Cascaded flare system means a series of flares connected to one
flare gas header system arranged with increasing pressure set points so
that discharges will be initially directed to the first flare in the
series (i.e., the primary flare). If the discharge pressure exceeds a
set point at which the flow to the primary flare would exceed the
primary flare's capacity, flow will be diverted to the second flare in
the series. Similarly, flow would be diverted to a third (or fourth)
flare if the pressure in the flare gas header system exceeds a
threshold where the flow to the first two (or three) flares would
exceed their capacities.
Co-fired process heater means a process heater that employs burners
that are designed to be supplied by both gaseous and liquid fuels on a
routine basis. Process heaters that have gas burners with emergency oil
back-up burners are not considered co-fired process heaters.
* * * * *
Corrective action means the design, operation and maintenance
changes that one takes consistent with good
[[Page 56465]]
engineering practice to reduce or eliminate the likelihood of the
recurrence of the primary cause and any other contributing cause(s) of
an event identified by a root cause analysis as having resulted in a
discharge of gases to an affected flare in excess of specified
thresholds.
Corrective action analysis means a description of all reasonable
interim and long-term measures, if any, that are available, and an
explanation of why the selected corrective action(s) is/are the best
alternative(s), including, but not limited to, considerations of cost
effectiveness, technical feasibility, safety and secondary impacts.
Delayed coking unit means a refinery process unit in which high
molecular weight petroleum derivatives are thermally cracked and
petroleum coke is produced in a series of closed, batch system
reactors. A delayed coking unit includes, but is not limited to, all of
the coke drums associated with a single fractionator; the fractionator,
including the bottoms receiver and the overhead condenser; the coke
drum cutting water and quench system, including the jet pump and coker
quench water tank; process piping and associated equipment such as
pumps, valves and connectors; and the coke drum blowdown recovery
compressor system.
Emergency flare means a flare that combusts gas exclusively
released as a result of malfunctions (and not startup, shutdown,
routine operations or any other cause) on four or fewer occasions in a
rolling 365-day period. For purposes of this rule, a flare cannot be
categorized as an emergency flare unless it maintains a water seal.
Flare means a combustion device that uses an uncontrolled volume of
air to burn gases. The flare includes the foundation, flare tip,
structural support, burner, igniter, flare controls, including air
injection or steam injection systems, flame arrestors and the flare gas
header system. In the case of an interconnected flare gas header
system, the flare includes each individual flare serviced by the
interconnected flare gas header system and the interconnected flare gas
header system.
Flare gas header system means all piping and knockout pots,
including those in a subheader system, used to collect and transport
gas to a flare either from a process unit or a pressure relief valve
from the fuel gas system, regardless of whether or not a flare gas
recovery system draws gas from the flare gas header system. The flare
gas header system includes piping inside the battery limit of a process
unit if the purpose of the piping is to transport gas to a flare or
knockout pot that is part of the flare.
Flare gas recovery system means a system of one or more
compressors, piping and the associated water seal, rupture disk or
similar device used to divert gas from the flare and direct the gas to
the fuel gas system or to a fuel gas combustion device.
Flexicoking unit means a refinery process unit in which high
molecular weight petroleum derivatives are thermally cracked and
petroleum coke is continuously produced and then gasified to produce a
synthetic fuel gas.
* * * * *
Fluid coking unit means a refinery process unit in which high
molecular weight petroleum derivatives are thermally cracked and
petroleum coke is continuously produced in a fluidized bed system. The
fluid coking unit includes the coking reactor, the coking burner, and
equipment for controlling air pollutant emissions and for heat recovery
on the fluid coking burner exhaust vent.
Forced draft process heater means a process heater in which the
combustion air is supplied under positive pressure produced by a fan at
any location in the inlet air line prior to the point where the
combustion air enters the process heater or air preheat. For the
purposes of this subpart, a process heater that uses fans at both the
inlet air side and the exhaust air side (i.e., balanced draft system)
is considered to be a forced draft process heater.
Fuel gas means any gas which is generated at a petroleum refinery
and which is combusted. Fuel gas includes natural gas when the natural
gas is combined and combusted in any proportion with a gas generated at
a refinery. Fuel gas does not include gases generated by catalytic
cracking unit catalyst regenerators, coke calciners (used to make
premium grade coke) and fluid coking burners, but does include gases
from flexicoking unit gasifiers and other gasifiers. Fuel gas does not
include vapors that are collected and combusted in a thermal oxidizer
or flare installed to control emissions from wastewater treatment units
other than those processing sour water, marine tank vessel loading
operations or asphalt processing units (i.e., asphalt blowing stills).
Fuel gas combustion device means any equipment, such as process
heaters and boilers, used to combust fuel gas. For the purposes of this
subpart, fuel gas combustion device does not include flares or
facilities in which gases are combusted to produce sulfur or sulfuric
acid.
* * * * *
Natural draft process heater means any process heater in which the
combustion air is supplied under ambient or negative pressure without
the use of an inlet air (forced draft) fan. For the purposes of this
subpart, a natural draft process heater is any process heater that is
not a forced draft process heater, including induced draft systems.
Non-emergency flare means any flare that is not an emergency flare
as defined in this subpart.
* * * * *
Petroleum refinery means any facility engaged in producing
gasoline, kerosene, distillate fuel oils, residual fuel oils,
lubricants, asphalt (bitumen) or other products through distillation of
petroleum or through redistillation, cracking or reforming of
unfinished petroleum derivatives. A facility that produces only oil
shale or tar sands-derived crude oil for further processing at a
petroleum refinery using only solvent extraction and/or distillation to
recover diluent is not a petroleum refinery.
Primary flare means the first flare in a cascaded flare system.
* * * * *
Process upset gas means any gas generated by a petroleum refinery
process unit or by ancillary equipment as a result of startup,
shutdown, upset or malfunction.
Purge gas means gas introduced between a flare's water seal and a
flare's tip to prevent oxygen infiltration (backflow) into the flare
tip. For flares with no water seals, the function of purge gas is
performed by sweep gas (i.e., flares without water seals do not use
purge gas).
* * * * *
Root cause analysis means an assessment conducted through a process
of investigation to determine the primary cause, and any other
contributing cause(s), of a discharge of gases in excess of specified
thresholds.
Secondary flare means a flare in a cascaded flare system that
provides additional flare capacity and pressure relief to a flare gas
system when the flare gas flow exceeds the capacity of the primary
flare. For purposes of this subpart, a secondary flare is characterized
by infrequent use and must maintain a water seal.
* * * * *
Sulfur recovery plant means all process units which recover sulfur
from H2S and/or SO2 from a common source of sour
gas produced at a petroleum
[[Page 56466]]
refinery. The sulfur recovery plant also includes sulfur pits used to
store the recovered sulfur product, but it does not include secondary
sulfur storage vessels or loading facilities downstream of the sulfur
pits. For example, a Claus sulfur recovery plant includes: Reactor
furnace and waste heat boiler, catalytic reactors, sulfur pits and, if
present, oxidation or reduction control systems or incinerator, thermal
oxidizer or similar combustion device. Multiple sulfur recovery units
are a single affected facility only when the units share the same
source of sour gas. Sulfur recovery plants that receive source gas from
completely segregated sour gas treatment systems are separate affected
facilities.
Sweep gas means the gas introduced in a flare gas header system to
maintain a constant flow of gas to prevent oxygen buildup in the flare
header. For flares with no water seals, sweep gas also performs the
function of preventing oxygen infiltration (backflow) into the flare
tip.
0
11. In Sec. 60.102a, lift the stay on paragraph (g) published December
22, 2008 (73 FR 78552).
0
12. Section 60.102a is amended by:
0
a. Revising paragraph (a);
0
b. Revising paragraph (f)(1)(ii);
0
c. Revising paragraph (g);
0
d. Removing and reserving paragraph (h); and
0
e. Revising paragraph (i).
The revisions read as follows:
Sec. 60.102a Emissions limitations.
(a) Each owner or operator that is subject to the requirements of
this subpart shall comply with the emissions limitations in paragraphs
(b) through (i) of this section on and after the date on which the
initial performance test, required by Sec. 60.8, is completed, but not
later than 60 days after achieving the maximum production rate at which
the affected facility will be operated or 180 days after initial
startup, whichever comes first.
* * * * *
(f) * * *
(1) * * *
(ii) For a sulfur recovery plant with a reduction control system
not followed by incineration, the owner or operator shall not discharge
or cause the discharge of any gases into the atmosphere in excess of
300 ppmv of reduced sulfur compounds and 10 ppmv of H2S,
each calculated as ppmv SO2 (dry basis) at 0-percent excess
air; or
* * * * *
(g) Each owner or operator of an affected fuel gas combustion
device shall comply with the emissions limits in paragraphs (g)(1) and
(2) of this section.
(1) Except as provided in (g)(1)(iii) of this section, for each
fuel gas combustion device, the owner or operator shall comply with
either the emission limit in paragraph (g)(1)(i) of this section or the
fuel gas concentration limit in paragraph (g)(1)(ii) of this section.
(i) The owner or operator shall not discharge or cause the
discharge of any gases into the atmosphere that contain SO2
in excess of 20 ppmv (dry basis, corrected to 0-percent excess air)
determined hourly on a 3-hour rolling average basis and SO2
in excess of 8 ppmv (dry basis, corrected to 0-percent excess air),
determined daily on a 365 successive calendar day rolling average
basis; or
(ii) The owner or operator shall not burn in any fuel gas
combustion device any fuel gas that contains H2S in excess
of 162 ppmv determined hourly on a 3-hour rolling average basis and
H2S in excess of 60 ppmv determined daily on a 365
successive calendar day rolling average basis.
(iii) The combustion in a portable generator of fuel gas released
as a result of tank degassing and/or cleaning is exempt from the
emissions limits in paragraphs (g)(1)(i) and (ii) of this section.
(2) For each process heater with a rated capacity of greater than
40 million British thermal units per hour (MMBtu/hr) on a higher
heating value basis, the owner or operator shall not discharge to the
atmosphere any emissions of NOX in excess of the applicable
limits in paragraphs (g)(2)(i) through (iv) of this section.
(i) For each natural draft process heater, comply with the limit in
either paragraph (g)(2)(i)(A) or (B) of this section. The owner or
operator may comply with either limit at any time, provided that the
appropriate parameters for each alternative are monitored as specified
in Sec. 60.107a; if fuel gas composition is not monitored as specified
in Sec. 60.107a(d), the owner or operator must comply with the
concentration limits in paragraph (g)(2)(i)(A) of this section.
(A) 40 ppmv (dry basis, corrected to 0-percent excess air)
determined daily on a 30-day rolling average basis; or
(B) 0.040 pounds per million British thermal units (lb/MMBtu)
higher heating value basis determined daily on a 30-day rolling average
basis.
(ii) For each forced draft process heater, comply with the limit in
either paragraph (g)(2)(ii)(A) or (B) of this section. The owner or
operator may comply with either limit at any time, provided that the
appropriate parameters for each alternative are monitored as specified
in Sec. 60.107a; if fuel gas composition is not monitored as specified
in Sec. 60.107a(d), the owner or operator must comply with the
concentration limits in paragraph (g)(2)(ii)(A) of this section.
(A) 60 ppmv (dry basis, corrected to 0-percent excess air)
determined daily on a 30-day rolling average basis; or
(B) 0.060 lb/MMBtu higher heating value basis determined daily on a
30-day rolling average basis.
(iii) For each co-fired natural draft process heater, comply with
the limit in either paragraph (g)(2)(iii)(A) or (B) of this section.
The owner or operator must choose one of the emissions limits with
which to comply at all times:
(A) 150 ppmv (dry basis, corrected to 0-percent excess air)
determined daily on a 30 successive operating day rolling average
basis; or
(B) The daily average emissions limit calculated using Equation 3
of this section:
[GRAPHIC] [TIFF OMITTED] TR12SE12.001
Where:
ERNOx = Daily allowable average emission rate of
NOX, lb/MMBtu (higher heating value basis);
Qgas = Daily average volumetric flow rate of fuel gas,
standard cubic feet per day (scf/day);
Qoil = Daily average volumetric flow rate of fuel oil,
scf/day;
HHVgas = Daily average higher heating value of gas fired
to the process heater, MMBtu/scf; and
HHVoil = Daily average higher heating value of fuel oil
fired to the process heater, MMBtu/scf.
[[Page 56467]]
(iv) For each co-fired forced draft process heater, comply with the
limit in either paragraph (g)(2)(iv)(A) or (B) of this section. The
owner or operator must choose one of the emissions limits with which to
comply at all times:
(A) 150 ppmv (dry basis, corrected to 0-percent excess air)
determined daily on a 30 successive operating day rolling average
basis; or
(B) The daily average emissions limit calculated using Equation 4
of this section:
[GRAPHIC] [TIFF OMITTED] TR12SE12.002
Where:
ERNOx = Daily allowable average emission rate of
NOX, lb/MMBtu (higher heating value basis);
Qgas = Daily average volumetric flow rate of fuel gas,
scf/day;
Qoil = Daily average volumetric flow rate of fuel oil,
scf/day;
HHVgas = Daily average higher heating value of gas fired
to the process heater, MMBtu/scf; and
HHVoil = Daily average higher heating value of fuel oil
fired to the process heater, MMBtu/scf.
(h) [Reserved]
(i) For a process heater that meets any of the criteria of
paragraphs (i)(1)(i) through (iv) of this section, an owner or operator
may request approval from the Administrator for a NOX
emissions limit which shall apply specifically to that affected
facility. The request shall include information as described in
paragraph (i)(2) of this section. The request shall be submitted and
followed as described in paragraph (i)(3) of this section.
(1) A process heater that meets one of the criteria in paragraphs
(i)(1)(i) through (iv) of this section may apply for a site-specific
NOX emissions limit:
(i) A modified or reconstructed process heater that lacks
sufficient space to accommodate installation and proper operation of
combustion modification-based technology (e.g., ultra-low
NOX burners); or
(ii) A modified or reconstructed process heater that has downwardly
firing induced draft burners; or
(iii) A co-fired process heater; or
(iv) A process heater operating at reduced firing conditions for an
extended period of time (i.e., operating in turndown mode). The site-
specific NOX emissions limit will only apply for those
operating conditions.
(2) The request shall include sufficient and appropriate data, as
determined by the Administrator, to allow the Administrator to confirm
that the process heater is unable to comply with the applicable
NOX emissions limit in paragraph (g)(2) of this section. At
a minimum, the request shall contain the information described in
paragraphs (i)(2)(i) through (iv) of this section.
(i) The design and dimensions of the process heater, evaluation of
available combustion modification-based technology, description of fuel
gas and, if applicable, fuel oil characteristics, information regarding
the combustion conditions (temperature, oxygen content, firing rates)
and other information needed to demonstrate that the process heater
meets one of the four classes of process heaters listed in paragraph
(i)(1) of this section.
(ii) An explanation of how the data in paragraph (i)(2)(i)
demonstrate that ultra-low NOX burners, flue gas
recirculation, control of excess air or other combustion modification-
based technology (including combinations of these combustion
modification-based technologies) cannot be used to meet the applicable
emissions limit in paragraph (g)(2) of this section.
(iii) Results of a performance test conducted under representative
conditions using the applicable methods specified in Sec. 60.104a(i)
to demonstrate the performance of the technology the owner or operator
will use to minimize NOX emissions.
(iv) The means by which the owner or operator will document
continuous compliance with the site-specific emissions limit.
(3) The request shall be submitted and followed as described in
paragraphs (i)(3)(i) through (iii) of this section.
(i) The owner or operator of a process heater that meets one of the
criteria in paragraphs (i)(1)(i) through (iv) of this section may
request approval from the Administrator within 180 days after initial
startup of the process heater for a NOX emissions limit
which shall apply specifically to that affected facility.
(ii) The request must be submitted to the Administrator for
approval. The owner or operator must comply with the request as
submitted until it is approved.
(iii) The request shall also be submitted to the following address:
U.S. Environmental Protection Agency, Office of Air Quality Planning
and Standards, Sector Policies and Programs Division, U.S. EPA Mailroom
(E143-01), Attention: Refinery Sector Lead, 109 T.W. Alexander Drive,
Research Triangle Park, NC 27711. Electronic copies in lieu of hard
copies may also be submitted to refinerynsps@epa.gov.
(4) The approval process for a request for a facility-specific
NOX emissions limit is described in paragraphs (i)(4)(i)
through (iii) of this section.
(i) Approval by the Administrator of a facility-specific
NOX emissions limit request will be based on the
completeness, accuracy and reasonableness of the request. Factors that
the EPA will consider in reviewing the request for approval include,
but are not limited to, the following:
(A) A demonstration that the process heater meets one of the four
classes of process heaters outlined in paragraphs (i)(1) of this
section;
(B) A description of the low-NOX burner designs and
other combustion modifications considered for reducing NOX
emissions;
(C) The combustion modification option selected; and
(D) The operating conditions (firing rate, heater box temperature
and excess oxygen concentration) at which the NOX emission
level was established.
(ii) If the request is approved by the Administrator, a facility-
specific NOX emissions limit will be established at the
NOX emission level demonstrated in the approved request.
(iii) If the Administrator finds any deficiencies in the request,
the request must be revised to address the deficiencies and be re-
submitted for approval.
0
13. Section 60.103a is revised to read as follows:
Sec. 60.103a Design, equipment, work practice or operational
standards.
(a) Except as provided in paragraph (g) of this section, each owner
or operator that operates a flare that is subject to this subpart shall
develop and implement a written flare management plan no later than the
date specified in paragraph (b) of this section. The flare management
plan must include the information described in paragraphs (a)(1)
through (7) of this section.
[[Page 56468]]
(1) A listing of all refinery process units, ancillary equipment,
and fuel gas systems connected to the flare for each affected flare.
(2) An assessment of whether discharges to affected flares from
these process units, ancillary equipment and fuel gas systems can be
minimized. The flare minimization assessment must (at a minimum)
consider the items in paragraphs (a)(2)(i) through (iv) of this
section. The assessment must provide clear rationale in terms of costs
(capital and annual operating), natural gas offset credits (if
applicable), technical feasibility, secondary environmental impacts and
safety considerations for the selected minimization alternative(s) or a
statement, with justifications, that flow reduction could not be
achieved. Based upon the assessment, each owner or operator of an
affected flare shall identify the minimization alternatives that it has
implemented by the due date of the flare management plan and shall
include a schedule for the prompt implementation of any selected
measures that cannot reasonably be completed as of that date.
(i) Elimination of process gas discharge to the flare through
process operating changes or gas recovery at the source.
(ii) Reduction of the volume of process gas to the flare through
process operating changes.
(iii) Installation of a flare gas recovery system or, for
facilities that are fuel gas rich, a flare gas recovery system and a
co-generation unit or combined heat and power unit.
(iv) Minimization of sweep gas flow rates and, for flares with
water seals, purge gas flow rates.
(3) A description of each affected flare containing the information
in paragraphs (a)(3)(i) through (vii) of this section.
(i) A general description of the flare, including the information
in paragraphs (a)(3)(i)(A) through (G) of this section.
(A) Whether it is a ground flare or elevated (including height).
(B) The type of assist system (e.g., air, steam, pressure, non-
assisted).
(C) Whether it is simple or complex flare tip (e.g., staged,
sequential).
(D) Whether the flare is part of a cascaded flare system (and if
so, whether the flare is primary or secondary).
(E) Whether the flare serves as a backup to another flare.
(F) Whether the flare is an emergency flare or a non-emergency
flare.
(G) Whether the flare is equipped with a flare gas recovery system.
(ii) Description and simple process flow diagram showing the
interconnection of the following components of the flare: flare tip
(date installed, manufacturer, nominal and effective tip diameter, tip
drawing); knockout or surge drum(s) or pot(s) (including dimensions and
design capacities); flare header(s) and subheader(s); assist system;
and ignition system.
(iii) Flare design parameters, including the maximum vent gas flow
rate; minimum sweep gas flow rate; minimum purge gas flow rate (if
any); maximum supplemental gas flow rate; maximum pilot gas flow rate;
and, if the flare is steam-assisted, minimum total steam rate.
(iv) Description and simple process flow diagram showing all gas
lines (including flare, purge (if applicable), sweep, supplemental and
pilot gas) that are associated with the flare. For purge, sweep,
supplemental and pilot gas, identify the type of gas used. Designate
which lines are exempt from sulfur, H2S or flow monitoring
and why (e.g., natural gas, inherently low sulfur, pilot gas).
Designate which lines are monitored and identify on the process flow
diagram the location and type of each monitor.
(v) For each flow rate, H2S, sulfur content, pressure or
water seal monitor identified in paragraph (a)(3)(iv) of this section,
provide a detailed description of the manufacturer's specifications,
including, but not limited to, make, model, type, range, precision,
accuracy, calibration, maintenance and quality assurance procedures.
(vi) For emergency flares, secondary flares and flares equipped
with a flare gas recovery system designed, sized and operated to
capture all flows except those resulting from startup, shutdown or
malfunction:
(A) Description of the water seal, including the operating range
for the liquid level.
(B) Designation of the monitoring option elected (flow and sulfur
monitoring or pressure and water seal liquid level monitoring).
(vii) For flares equipped with a flare gas recovery system:
(A) A description of the flare gas recovery system, including
number of compressors and capacity of each compressor.
(B) A description of the monitoring parameters used to quantify the
amount of flare gas recovered.
(C) For systems with staged compressors, the maximum time period
required to begin gas recovery with the secondary compressor(s), the
monitoring parameters and procedures used to minimize the duration of
releases during compressor staging and a justification for why the
maximum time period cannot be further reduced.
(4) An evaluation of the baseline flow to the flare. The baseline
flow to the flare must be determined after implementing the
minimization assessment in paragraph (a)(2) of this section. Baseline
flows do not include pilot gas flow or purge gas flow (i.e., gas
introduced after the flare's water seal) provided these gas flows
remain reasonably constant (i.e., separate flow monitors for these
streams are not required). Separate baseline flow rates may be
established for different operating conditions provided that the
management plan includes:
(i) A primary baseline flow rate that will be used as the default
baseline for all conditions except those specifically delineated in the
plan;
(ii) A description of each special condition for which an alternate
baseline is established, including the rationale for each alternate
baseline, the daily flow for each alternate baseline and the expected
duration of the special conditions for each alternate baseline; and
(iii) Procedures to minimize discharges to the affected flare
during each special condition described in paragraph (a)(4)(ii) of this
section, unless procedures are already developed for these cases under
paragraph (a)(5) through (7) of this section, as applicable.
(5) Procedures to minimize or eliminate discharges to the flare
during the planned startup and shutdown of the refinery process units
and ancillary equipment that are connected to the affected flare,
together with a schedule for the prompt implementation of any
procedures that cannot reasonably be implemented as of the date of the
submission of the flare management plan.
(6) Procedures to reduce flaring in cases of fuel gas imbalance
(i.e., excess fuel gas for the refinery's energy needs), together with
a schedule for the prompt implementation of any procedures that cannot
reasonably be implemented as of the date of the submission of the flare
management plan.
(7) For flares equipped with flare gas recovery systems, procedures
to minimize the frequency and duration of outages of the flare gas
recovery system and procedures to minimize the volume of gas flared
during such outages, together with a schedule for the prompt
implementation of any procedures that cannot reasonably be implemented
as of the date of the submission of the flare management plan.
(b) Except as provided in paragraph (g) of this section, each owner
or
[[Page 56469]]
operator required to develop and implement a written flare management
plan as described in paragraph (a) of this section must submit the plan
to the Administrator as described in paragraphs (b)(1) through (3) of
this section.
(1) The owner or operator of a newly constructed or reconstructed
flare must develop and implement the flare management plan by no later
than the date that the flare becomes an affected facility subject to
this subpart, except for the selected minimization alternatives in
paragraph (a)(2) and/or the procedures in paragraphs (a)(5) though
(a)(7) of this section that cannot reasonably be implemented by that
date, which the owner or operator must implement in accordance with the
schedule in the flare management plan. The owner or operator of a
modified flare must develop and implement the flare management plan by
no later than November 11, 2015 or upon startup of the modified flare,
whichever is later.
(2) The owner or operator must comply with the plan as submitted by
the date specified in paragraph (b)(1) of this section. The plan should
be updated periodically to account for changes in the operation of the
flare, such as new connections to the flare or the installation of a
flare gas recovery system, but the plan need be re-submitted to the
Administrator only if the owner or operator adds an alternative
baseline flow rate, revises an existing baseline as described in
paragraph (a)(4) of this section, installs a flare gas recovery system
or is required to change flare designations and monitoring methods as
described in Sec. 60.107a(g). The owner or operator must comply with
the updated plan as submitted.
(3) All versions of the plan submitted to the Administrator shall
also be submitted to the following address: U.S. Environmental
Protection Agency, Office of Air Quality Planning and Standards, Sector
Policies and Programs Division, U.S. EPA Mailroom (E143-01), Attention:
Refinery Sector Lead, 109 T.W. Alexander Drive, Research Triangle Park,
NC 27711. Electronic copies in lieu of hard copies may also be
submitted to refinerynsps@epa.gov.
(c) Except as provided in paragraphs (f) and (g) of this section,
each owner or operator that operates a fuel gas combustion device,
flare or sulfur recovery plant subject to this subpart shall conduct a
root cause analysis and a corrective action analysis for each of the
conditions specified in paragraphs (c)(1) through (3) of this section.
(1) For a flare:
(i) Any time the SO2 emissions exceed 227 kilograms (kg)
(500 lb) in any 24-hour period; or
(ii) Any discharge to the flare in excess of 14,160 standard cubic
meters (m\3\) (500,000 standard cubic feet (scf)) above the baseline,
determined in paragraph (a)(4) of this section, in any 24-hour period;
or
(iii) If the monitoring alternative in Sec. 60.107a(g) is elected,
any period when the flare gas line pressure exceeds the water seal
liquid depth, except for periods attributable to compressor staging
that do not exceed the staging time specified in paragraph
(a)(3)(vii)(C) of this section.
(2) For a fuel gas combustion device, each exceedance of an
applicable short-term emissions limit in Sec. 60.102a(g)(1) if the
SO2 discharge to the atmosphere is 227 kg (500 lb) greater
than the amount that would have been emitted if the emissions limits
had been met during one or more consecutive periods of excess emissions
or any 24-hour period, whichever is shorter.
(3) For a sulfur recovery plant, each time the SO2
emissions are more than 227 kg (500 lb) greater than the amount that
would have been emitted if the SO2 or reduced sulfur
concentration was equal to the applicable emissions limit in Sec.
60.102a(f)(1) or (2) during one or more consecutive periods of excess
emissions or any 24-hour period, whichever is shorter.
(d) Except as provided in paragraphs (f) and (g) of this section, a
root cause analysis and corrective action analysis must be completed as
soon as possible, but no later than 45 days after a discharge meeting
one of the conditions specified in paragraphs (c)(1) through (3) of
this section. Special circumstances affecting the number of root cause
analyses and/or corrective action analyses are provided in paragraphs
(d)(1) through (5) of this section.
(1) If a single continuous discharge meets any of the conditions
specified in paragraphs (c)(1) through (3) of this section for 2 or
more consecutive 24-hour periods, a single root cause analysis and
corrective action analysis may be conducted.
(2) If a single discharge from a flare triggers a root cause
analysis based on more than one of the conditions specified in
paragraphs (c)(1)(i) through (iii) of this section, a single root cause
analysis and corrective action analysis may be conducted.
(3) If the discharge from a flare is the result of a planned
startup or shutdown of a refinery process unit or ancillary equipment
connected to the affected flare and the procedures in paragraph (a)(5)
of this section were followed, a root cause analysis and corrective
action analysis is not required; however, the discharge must be
recorded as described in Sec. 60.108a(c)(6) and reported as described
in Sec. 60.108a(d)(5).
(4) If both the primary and secondary flare in a cascaded flare
system meet any of the conditions specified in paragraphs (c)(1)(i)
through (iii) of this section in the same 24-hour period, a single root
cause analysis and corrective action analysis may be conducted.
(5) Except as provided in paragraph (d)(4) of this section, if
discharges occur that meet any of the conditions specified in
paragraphs (c)(1) through (3) of this section for more than one
affected facility in the same 24-hour period, initial root cause
analyses shall be conducted for each affected facility. If the initial
root cause analyses indicate that the discharges have the same root
cause(s), the initial root cause analyses can be recorded as a single
root cause analysis and a single corrective action analysis may be
conducted.
(e) Except as provided in paragraphs (f) and (g) of this section,
each owner or operator of a fuel gas combustion device, flare or sulfur
recovery plant subject to this subpart shall implement the corrective
action(s) identified in the corrective action analysis conducted
pursuant to paragraph (d) of this section in accordance with the
applicable requirements in paragraphs (e)(1) through (3) of this
section.
(1) All corrective action(s) must be implemented within 45 days of
the discharge for which the root cause and corrective action analyses
were required or as soon thereafter as practicable. If an owner or
operator concludes that corrective action should not be conducted, the
owner or operator shall record and explain the basis for that
conclusion no later than 45 days following the discharge as specified
in Sec. 60.108a(c)(6)(ix).
(2) For corrective actions that cannot be fully implemented within
45 days following the discharge for which the root cause and corrective
action analyses were required, the owner or operator shall develop an
implementation schedule to complete the corrective action(s) as soon as
practicable.
(3) No later than 45 days following the discharge for which a root
cause and corrective action analyses were required, the owner or
operator shall record the corrective action(s) completed to date, and,
for action(s) not already completed, a schedule for implementation,
including proposed commencement and completion dates as specified in
Sec. 60.108a(c)(6)(x).
[[Page 56470]]
(f) Modified flares shall comply with the requirements of
paragraphs (c) through (e) of this section by November 11, 2015 or at
startup of the modified flare, whichever is later. Modified flares that
were not affected facilities subject to subpart J of this part prior to
becoming affected facilities under Sec. 60.100a shall comply with the
requirements of paragraph (h) of this section and the requirements of
Sec. 60.107a(a)(2) by November 11, 2015 or at startup of the modified
flare, whichever is later. Modified flares that were affected
facilities subject to subpart J of this part prior to becoming affected
facilities under Sec. 60.100a shall comply with the requirements of
paragraph (h) of this section and the requirements of Sec.
60.107a(a)(2) by November 13, 2012 or at startup of the modified flare,
whichever is later, except that modified flares that have accepted
applicability of subpart J under a federal consent decree shall comply
with the subpart J requirements as specified in the consent decree, but
shall comply with the requirements of paragraph (h) of this section and
the requirements of Sec. 60.107a(a)(2) by no later than November 11,
2015.
(g) An affected flare subject to this subpart located in the Bay
Area Air Quality Management District (BAAQMD) may elect to comply with
both BAAQMD Regulation 12, Rule 11 and BAAQMD Regulation 12, Rule 12 as
an alternative to complying with the requirements of paragraphs (a)
through (e) of this section. An affected flare subject to this subpart
located in the South Coast Air Quality Management District (SCAQMD) may
elect to comply with SCAQMD Rule 1118 as an alternative to complying
with the requirements of paragraphs (a) through (e) of this section.
The owner or operator of an affected flare must notify the
Administrator that the flare is in compliance with BAAQMD Regulation
12, Rule 11 and BAAQMD Regulation 12, Rule 12 or SCAQMD Rule 1118. The
owner or operator of an affected flare shall also submit the existing
flare management plan to the following address: U.S. Environmental
Protection Agency, Office of Air Quality Planning and Standards, Sector
Policies and Programs Division, U.S. EPA Mailroom (E143-01), Attention:
Refinery Sector Lead, 109 T.W. Alexander Drive, Research Triangle Park,
NC 27711. Electronic copies in lieu of hard copies may also be
submitted to refinerynsps@epa.gov.
(h) Each owner or operator shall not burn in any affected flare any
fuel gas that contains H2S in excess of 162 ppmv determined
hourly on a 3-hour rolling average basis. The combustion in a flare of
process upset gases or fuel gas that is released to the flare as a
result of relief valve leakage or other emergency malfunctions is
exempt from this limit.
(i) Each owner or operator of a delayed coking unit shall
depressure each coke drum to 5 lb per square inch gauge (psig) or less
prior to discharging the coke drum steam exhaust to the atmosphere.
Until the coke drum pressure reaches 5 psig, the coke drum steam
exhaust must be managed in an enclosed blowdown system and the
uncondensed vapor must either be recovered (e.g., sent to the delayed
coking unit fractionators) or vented to the fuel gas system, a fuel gas
combustion device or a flare.
(j) Alternative means of emission limitation. (1) Each owner or
operator subject to the provisions of this section may apply to the
Administrator for a determination of equivalence for any means of
emission limitation that achieves a reduction in emissions of a
specified pollutant at least equivalent to the reduction in emissions
of that pollutant achieved by the controls required in this section.
(2) Determination of equivalence to the design, equipment, work
practice or operational requirements of this section will be evaluated
by the following guidelines:
(i) Each owner or operator applying for a determination of
equivalence shall be responsible for collecting and verifying test data
to demonstrate the equivalence of the alternative means of emission
limitation.
(ii) For each affected facility for which a determination of
equivalence is requested, the emission reduction achieved by the
design, equipment, work practice or operational requirements shall be
demonstrated.
(iii) For each affected facility for which a determination of
equivalence is requested, the emission reduction achieved by the
alternative means of emission limitation shall be demonstrated.
(iv) Each owner or operator applying for a determination of
equivalence to a work practice standard shall commit in writing to work
practice(s) that provide for emission reductions equal to or greater
than the emission reductions achieved by the required work practice.
(v) The Administrator will compare the demonstrated emission
reduction for the alternative means of emission limitation to the
demonstrated emission reduction for the design, equipment, work
practice or operational requirements and, if applicable, will consider
the commitment in paragraph (j)(2)(iv) of this section.
(vi) The Administrator may condition the approval of the
alternative means of emission limitation on requirements that may be
necessary to ensure operation and maintenance to achieve the same
emissions reduction as the design, equipment, work practice or
operational requirements.
(3) An owner or operator may offer a unique approach to demonstrate
the equivalence of any equivalent means of emission limitation.
(4) Approval of the application for equivalence to the design,
equipment, work practice or operational requirements of this section
will be evaluated by the following guidelines:
(i) After a request for determination of equivalence is received,
the Administrator will publish a notice in the Federal Register and
provide the opportunity for public hearing if the Administrator judges
that the request may be approved.
(ii) After notice and opportunity for public hearing, the
Administrator will determine the equivalence of a means of emission
limitation and will publish the determination in the Federal Register.
(iii) Any equivalent means of emission limitations approved under
this section shall constitute a required work practice, equipment,
design or operational standard within the meaning of section 111(h)(1)
of the CAA.
(5) Manufacturers of equipment used to control emissions may apply
to the Administrator for determination of equivalence for any
alternative means of emission limitation that achieves a reduction in
emissions achieved by the equipment, design and operational
requirements of this section. The Administrator will make an
equivalence determination according to the provisions of paragraphs
(j)(2) through (4) of this section.
0
14. Section 60.104a is amended by:
0
a. Revising paragraph (a);
0
b. Revising paragraphs (d)(4)(ii), (d)(4)(iii), (d)(4)(v) and (d)(8);
0
c. Revising paragraph (f)(3);
0
d. Revising paragraph (h)(5)(iv);
0
e. Revising paragraph (i) introductory text;
0
f. Adding paragraphs (i)(6) through (i)(8);
0
g. Revising paragraph (j) introductory text and paragraph (j)(4)
introductory text; and
0
h. Revising paragraph (j)(4)(iv) to read as follows:
Sec. 60.104a Performance tests.
(a) The owner or operator shall conduct a performance test for each
FCCU, FCU, sulfur recovery plant, flare and fuel gas combustion device
to
[[Page 56471]]
demonstrate initial compliance with each applicable emissions limit in
Sec. 60.102a according to the requirements of Sec. 60.8. The
notification requirements of Sec. 60.8(d) apply to the initial
performance test and to subsequent performance tests required by
paragraph (b) of this section (or as required by the Administrator),
but does not apply to performance tests conducted for the purpose of
obtaining supplemental data because of continuous monitoring system
breakdowns, repairs, calibration checks and zero and span adjustments.
* * * * *
(d) * * *
(4) * * *
(ii) The emissions rate of PM (EPM) is computed for each
run using Equation 5 of this section:
[GRAPHIC] [TIFF OMITTED] TR12SE12.003
Where:
E = Emission rate of PM, g/kg (lb/1,000 lb) of coke burn-off;
cs = Concentration of total PM, grams per dry standard
cubic meter (g/dscm) (gr/dscf);
Qsd = Volumetric flow rate of effluent gas, dry standard
cubic meters per hour (dry standard cubic feet per hour);
Rc = Coke burn-off rate, kilograms per hour (kg/hr) [lb
per hour (lb/hr)] coke; and
K = Conversion factor, 1.0 grams per gram (7,000 grains per lb).
(iii) The coke burn-off rate (Rc) is computed for each
run using Equation 6 of this section:
[GRAPHIC] [TIFF OMITTED] TR12SE12.004
Where:
Rc = Coke burn-off rate, kg/hr (lb/hr);
Qr = Volumetric flow rate of exhaust gas from FCCU
regenerator or fluid coking burner before any emissions control or
energy recovery system that burns auxiliary fuel, dry standard cubic
meters per minute (dscm/min) [dry standard cubic feet per minute
(dscf/min)];
Qa = Volumetric flow rate of air to FCCU regenerator or
fluid coking burner, as determined from the unit's control room
instrumentation, dscm/min (dscf/min);
Qoxy = Volumetric flow rate of O2 enriched air
to FCCU regenerator or fluid coking unit, as determined from the
unit's control room instrumentation, dscm/min (dscf/min);
%CO2 = Carbon dioxide (CO2) concentration in
FCCU regenerator or fluid coking burner exhaust, percent by volume
(dry basis);
%CO = CO concentration in FCCU regenerator or fluid coking burner
exhaust, percent by volume (dry basis);
%O2 = O2 concentration in FCCU regenerator or
fluid coking burner exhaust, percent by volume (dry basis);
%Ooxy = O2 concentration in O2
enriched air stream inlet to the FCCU regenerator or fluid coking
burner, percent by volume (dry basis);
K1 = Material balance and conversion factor, 0.2982 (kg-
min)/(hr-dscm-%) [0.0186 (lb-min)/(hr-dscf-%)];
K2 = Material balance and conversion factor, 2.088 (kg-
min)/(hr-dscm) [0.1303 (lb-min)/(hr-dscf)]; and
K3 = Material balance and conversion factor, 0.0994 (kg-
min)/(hr-dscm-%) [0.00624 (lb-min)/(hr-dscf-%)].
* * * * *
(v) For subsequent calculations of coke burn-off rates or exhaust
gas flow rates, the volumetric flow rate of Qr is calculated
using average exhaust gas concentrations as measured by the monitors
required in Sec. 60.105a(b)(2), if applicable, using Equation 7 of
this section:
[GRAPHIC] [TIFF OMITTED] TR12SE12.005
Where:
Qr = Volumetric flow rate of exhaust gas from FCCU
regenerator or fluid coking burner before any emission control or
energy recovery system that burns auxiliary fuel, dscm/min (dscf/
min);
Qa = Volumetric flow rate of air to FCCU regenerator or
fluid coking burner, as determined from the unit's control room
instrumentation, dscm/min (dscf/min);
Qoxy = Volumetric flow rate of O2 enriched air
to FCCU regenerator or fluid coking unit, as determined from the
unit's control room instrumentation, dscm/min (dscf/min);
%CO2 = Carbon dioxide concentration in FCCU regenerator
or fluid coking burner exhaust, percent by volume (dry basis);
%CO = CO concentration FCCU regenerator or fluid coking burner
exhaust, percent by volume (dry basis). When no auxiliary fuel is
burned and a continuous CO monitor is not required in accordance
with Sec. 60.105a(h)(3), assume %CO to be zero;
%O2 = O2 concentration in FCCU regenerator or
fluid coking burner exhaust, percent by volume (dry basis); and
%Ooxy = O2 concentration in O2
enriched air stream inlet to the FCCU regenerator or fluid coking
burner, percent by volume (dry basis).
* * * * *
(8) The owner or operator shall adjust PM, NOX,
SO2 and CO pollutant concentrations to 0-percent excess air
or 0-percent O2 using Equation 8 of this section:
[[Page 56472]]
[GRAPHIC] [TIFF OMITTED] TR12SE12.006
Where:
Cadj = pollutant concentration adjusted to 0-percent
excess air or O2, parts per million (ppm) or g/dscm;
Cmeas = pollutant concentration measured on a dry basis,
ppm or g/dscm;
20.9c = 20.9 percent O2-0.0 percent
O2 (defined O2 correction basis), percent;
20.9 = O2 concentration in air, percent; and
%O2 = O2 concentration measured on a dry
basis, percent.
* * * * *
(f) * * *
(3) Compute the site-specific limit using Equation 9 of this
section:
[GRAPHIC] [TIFF OMITTED] TR12SE12.007
Where:
Opacity limit = Maximum permissible 3-hour average opacity, percent,
or 10 percent, whichever is greater;
Opacityst = Hourly average opacity measured during the
source test, percent; and
PMEmRst = PM emission rate measured during the source
test, lb/1,000 lb coke burn.
* * * * *
(h) * * *
(5) * * *
(iv) The owner or operator shall use Equation 8 of this section to
adjust pollutant concentrations to 0-percent O2 or 0-
percent excess air.
(i) The owner or operator shall determine compliance with the
SO2 and NOX emissions limits in Sec. 60.102a(g)
for a fuel gas combustion device according to the following test
methods and procedures:
* * * * *
(6) For process heaters with a rated heat capacity between 40 and
100 MMBtu/hr that elect to demonstrate continuous compliance with a
maximum excess oxygen limit as provided in Sec. 60.107a(c)(6) or
(d)(8), the owner or operator shall establish the O2
operating limit or O2 operating curve based on the
performance test results according to the requirements in paragraph
(i)(6)(i) or (ii) of this section, respectively.
(i) If a single O2 operating limit will be used:
(A) Conduct the performance test following the methods provided in
paragraphs (i)(1), (2), (3) and (5) of this section when the process
heater is firing at no less than 70 percent of the rated heat capacity.
For co-fired process heaters, conduct at least one of the test runs
while the process heater is being supplied by both fuel gas and fuel
oil and conduct at least one of the test runs while the process heater
is being supplied solely by fuel gas.
(B) Each test will consist of three test runs. Calculate the
NOX concentration for the performance test as the average of
the NOX concentrations from each of the three test runs. If
the NOX concentration for the performance test is less than
or equal to the numerical value of the applicable NOX
emissions limit (regardless of averaging time), then the test is
considered to be a valid test.
(C) Determine the average O2 concentration for each test
run of a valid test.
(D) Calculate the O2 operating limit as the average
O2 concentration of the three test runs from a valid test.
(ii) If an O2 operating curve will be used:
(A) Conduct a performance test following the methods provided in
paragraphs (i)(1), (2), (3) and (5) of this section at a representative
condition for each operating range for which different O2
operating limits will be established. Different operating conditions
may be defined as different firing rates (e.g., above 50 percent of
rated heat capacity and at or below 50 percent of rated heat capacity)
and/or, for co-fired process heaters, different fuel mixtures (e.g.,
primarily gas fired, primarily oil fired, and equally co-fired, i.e.,
approximately 50 percent of the input heating value is from fuel gas
and approximately 50 percent of the input heating value is from fuel
oil). Performance tests for different operating ranges may be conducted
at different times.
(B) Each test will consist of three test runs. Calculate the
NOX concentration for the performance test as the average of
the NOX concentrations from each of the three test runs. If
the NOX concentration for the performance test is less than
or equal to the numerical value of the applicable NOX
emissions limit (regardless of averaging time), then the test is
considered to be a valid test.
(C) If an operating curve is developed for different firing rates,
conduct at least one test when the process heater is firing at no less
than 70 percent of the rated heat capacity and at least one test under
turndown conditions (i.e., when the process heater is firing at 50
percent or less of the rated heat capacity). If O2 operating
limits are developed for co-fired process heaters based only on overall
firing rates (and not by fuel mixtures), conduct at least one of the
test runs for each test while the process heater is being supplied by
both fuel gas and fuel oil and conduct at least one of the test runs
while the process heater is being supplied solely by fuel gas.
(D) Determine the average O2 concentration for each test
run of a valid test.
(E) Calculate the O2 operating limit for each operating
range as the average O2 concentration of the three test runs
from a valid test conducted at the representative conditions for that
given operating range.
(F) Identify the firing rates for which the different operating
limits apply. If only two operating limits are established based on
firing rates, the O2 operating limits established when the
process heater is firing at no less than 70 percent of the rated heat
capacity must apply when the process heater is firing above 50 percent
of the rated heat capacity and the O2 operating limits
established for turndown conditions must apply when the process heater
is firing at 50 percent or less of the rated heat capacity.
(G) Operating limits associated with each interval will be valid
for 2 years or until another operating limit is established for that
interval based on a more recent performance test specific for that
interval, whichever occurs first. Owners and operators must use the
operating limits determined for a given interval based on the most
recent performance test conducted for that interval.
(7) The owner or operator of a process heater complying with a
NOX limit in terms of lb/MMBtu as provided in Sec.
60.102a(g)(2)(i)(B), (g)(2)(ii)(B), (g)(2)(iii)(B) or (g)(2)(iv)(B) or
a process heater with a rated heat capacity between 40 and 100 MMBtu/hr
that
[[Page 56473]]
elects to demonstrate continuous compliance with a maximum excess
O2 limit, as provided in Sec. 60.107a(c)(6) or (d)(8),
shall determine heat input to the process heater in MMBtu/hr during
each performance test run by measuring fuel gas flow rate, fuel oil
flow rate (as applicable) and heating value content according to the
methods provided in Sec. 60.107a(d)(5), (d)(6), and (d)(4) or (d)(7),
respectively.
(8) The owner or operator shall use Equation 8 of this section to
adjust pollutant concentrations to 0-percent O2 or 0-
percent excess air.
(j) The owner or operator shall determine compliance with the
applicable H2S emissions limit in Sec. 60.102a(g)(1) for a
fuel gas combustion device or the concentration requirement in Sec.
60.103a(h) for a flare according to the following test methods and
procedures:
* * * * *
(4) EPA Method 11, 15 or 15A of Appendix A-5 to part 60 or EPA
Method 16 of Appendix A-6 to part 60 for determining the H2S
concentration for affected facilities using an H2S monitor
as specified in Sec. 60.107a(a)(2). The method ANSI/ASME PTC 19.10-
1981 (incorporated by reference--see Sec. 60.17) is an acceptable
alternative to EPA Method 15A of Appendix A-5 to part 60. The owner or
operator may demonstrate compliance based on the mixture used in the
fuel gas combustion device or flare or for each individual fuel gas
stream used in the fuel gas combustion device or flare.
* * * * *
(iv) If monitoring is conducted at a single point in a common
source of fuel gas as allowed under Sec. 60.107a(a)(2)(iv), only one
performance test is required. That is, performance tests are not
required when a new affected fuel gas combustion device or flare is
added to a common source of fuel gas that previously demonstrated
compliance.
0
15. Section 60.105a is amended by:
0
a. Revising paragraph (b) introductory text, and paragraph (b)(1)
introductory text, and paragraphs (b)(1)(ii)(A), (b)(2)(i) and
(b)(2)(ii); and
0
b. Revising paragraph (i)(5) to read as follows:
Sec. 60.105a Monitoring of emissions and operations for fluid
catalytic cracking units (FCCU) and fluid coking units (FCU).
* * * * *
(b) Control device operating parameters. Each owner or operator of
a FCCU or FCU subject to the PM per coke burn-off emissions limit in
Sec. 60.102a(b)(1) that uses a control device other than fabric filter
or cyclone shall comply with the requirements in paragraphs (b)(1) and
(2) of this section.
(1) The owner or operator shall install, operate and maintain
continuous parameter monitor systems (CPMS) to measure and record
operating parameters for each control device according to the
applicable requirements in paragraphs (b)(1)(i) through (v) of this
section.
* * * * *
(ii) * * *
(A) As an alternative to pressure drop, the owner or operator of a
jet ejector type wet scrubber or other type of wet scrubber equipped
with atomizing spray nozzles must conduct a daily check of the air or
water pressure to the spray nozzles and record the results of each
check.
* * * * *
(2) * * *
(i) The owner or operator shall install, operate and maintain each
monitor according to Performance Specifications 3 and 4 of Appendix B
to part 60.
(ii) The owner or operator shall conduct performance evaluations of
each CO2, O2 and CO monitor according to the
requirements in Sec. 60.13(c) and Performance Specifications 3 and 4
of Appendix B to part 60. The owner or operator shall use EPA Method 3
of Appendix A-3 to part 60 and EPA Method 10, 10A or 10B of Appendix A-
4 to part 60 for conducting the relative accuracy evaluations.
* * * * *
(i) * * *
(5) All rolling 7-day periods during which the average
concentration of SO2 as measured by the SO2 CEMS
under Sec. 60.105a(g) exceeds 50 ppmv, and all rolling 365-day periods
during which the average concentration of SO2 as measured by
the SO2 CEMS exceeds 25 ppmv.
* * * * *
0
16. In Sec. 60.107a, lift the stay on paragraphs (d) and (e) published
December 22, 2008 (73 FR 78552).
0
17. Section 60.107a is amended by:
0
a. Revising the section heading;
0
b. Revising paragraph (a) introductory text, paragraph (a)(1)
introductory text, paragraph (a)(2) introductory text, (a)(2)(i),
(a)(2)(iv) and paragraph (a)(3) introductory text;
0
c. Adding paragraphs (a)(2)(v) and (a)(2)(vi);
0
d. Revising paragraph (b) introductory text and paragraphs (b)(1)(i),
(b)(1)(v) and (b)(3)(iii);
0
e. Revising paragraph (c) introductory text and paragraphs (c)(1) and
(c)(6);
0
f. Redesignating paragraphs (d), (e), and (f) as paragraphs (e), (f)
and (i), respectively;
0
g. Adding a new paragraph (d);
0
h. Revising newly redesignated paragraph (e);
0
i. Revising newly redesignated paragraph (f);
0
j. Adding a new paragraph (g);
0
k. Adding a new paragraph (h); and
0
l. Revising newly redesignated paragraph (i).
The revisions and additions read as follows:
Sec. 60.107a Monitoring of emissions and operations for fuel gas
combustion devices and flares.
(a) Fuel gas combustion devices subject to SO2 or
H2S limit and flares subject to H2S concentration
requirements. The owner or operator of a fuel gas combustion device
that is subject to Sec. 60.102a(g)(1) and elects to comply with the
SO2 emission limits in Sec. 60.102a(g)(1)(i) shall comply
with the requirements in paragraph (a)(1) of this section. The owner or
operator of a fuel gas combustion device that is subject to Sec.
60.102a(g)(1) and elects to comply with the H2S
concentration limits in Sec. 60.102a(g)(1)(ii) or a flare that is
subject to the H2S concentration requirement in Sec.
60.103a(h) shall comply with paragraph (a)(2) of this section.
(1) The owner or operator of a fuel gas combustion device that
elects to comply with the SO2 emissions limits in Sec.
60.102a(g)(1)(i) shall install, operate, calibrate and maintain an
instrument for continuously monitoring and recording the concentration
(dry basis, 0-percent excess air) of SO2 emissions into the
atmosphere. The monitor must include an O2 monitor for
correcting the data for excess air.
* * * * *
(2) The owner or operator of a fuel gas combustion device that
elects to comply with the H2S concentration limits in Sec.
60.102a(g)(1)(ii) or a flare that is subject to the H2S
concentration requirement in Sec. 60.103a(h) shall install, operate,
calibrate and maintain an instrument for continuously monitoring and
recording the concentration by volume (dry basis) of H2S in
the fuel gases before being burned in any fuel gas combustion device or
flare.
(i) The owner or operator shall install, operate and maintain each
H2S monitor according to Performance Specification 7 of
Appendix B to part 60. The span value for this instrument is 300 ppmv
H2S.
* * * * *
(iv) Fuel gas combustion devices or flares having a common source
of fuel gas may be monitored at only one location, if monitoring at
this location accurately represents the concentration
[[Page 56474]]
of H2S in the fuel gas being burned in the respective fuel
gas combustion devices or flares.
(v) The owner or operator of a flare subject to Sec. 60.103a(c)
through (e) may use the instrument required in paragraph (e)(1) of this
section to demonstrate compliance with the H2S concentration
requirement in Sec. 60.103a(h) if the owner or operator complies with
the requirements of paragraph (e)(1)(i) through (iv) and if the
instrument has a span (or dual span, if necessary) capable of
accurately measuring concentrations between 20 and 300 ppmv. If the
instrument required in paragraph (e)(1) of this section is used to
demonstrate compliance with the H2S concentration
requirement, the concentration directly measured by the instrument must
meet the numeric concentration in Sec. 60.103a(h).
(vi) The owner or operator of modified flare that meets all three
criteria in paragraphs (a)(2)(vi)(A) through (C) of this section shall
comply with the requirements of paragraphs (a)(2)(i) through (v) of
this section no later than November 11, 2015. The owner or operator
shall comply with the approved alternative monitoring plan or plans
pursuant to Sec. 60.13(i) until the flare is in compliance with
requirements of paragraphs (a)(2)(i) through (v) of this section.
(A) The flare was an affected facility subject to subpart J of this
part prior to becoming an affected facility under Sec. 60.100a.
(B) The owner or operator had an approved alternative monitoring
plan or plans pursuant to Sec. 60.13(i) for all fuel gases combusted
in the flare.
(C) The flare did not have in place on or before September 12, 2012
an instrument for continuously monitoring and recording the
concentration by volume (dry basis) of H2S in the fuel gases
that is capable of complying with the requirements of paragraphs
(a)(2)(i) through (v) of this section.
(3) The owner or operator of a fuel gas combustion device or flare
is not required to comply with paragraph (a)(1) or (2) of this section
for fuel gas streams that are exempt under Sec. Sec.
60.102a(g)(1)(iii) or 60.103a(h) or, for fuel gas streams combusted in
a process heater, other fuel gas combustion device or flare that are
inherently low in sulfur content. Fuel gas streams meeting one of the
requirements in paragraphs (a)(3)(i) through (iv) of this section will
be considered inherently low in sulfur content.
* * * * *
(b) Exemption from H2S monitoring requirements for low-
sulfur fuel gas streams. The owner or operator of a fuel gas combustion
device or flare may apply for an exemption from the H2S
monitoring requirements in paragraph (a)(2) of this section for a fuel
gas stream that is inherently low in sulfur content. A fuel gas stream
that is demonstrated to be low-sulfur is exempt from the monitoring
requirements of paragraphs (a)(1) and (2) of this section until there
are changes in operating conditions or stream composition.
(1) * * *
(i) A description of the fuel gas stream/system to be considered,
including submission of a portion of the appropriate piping diagrams
indicating the boundaries of the fuel gas stream/system and the
affected fuel gas combustion device(s) or flare(s) to be considered;
* * * * *
(v) A description of how the 2 weeks (or seven samples for
infrequently operated fuel gas streams/systems) of monitoring results
compares to the typical range of H2S concentration (fuel
quality) expected for the fuel gas stream/system going to the affected
fuel gas combustion device or flare (e.g., the 2 weeks of daily
detector tube results for a frequently operated loading rack included
the entire range of products loaded out and, therefore, should be
representative of typical operating conditions affecting H2S
content in the fuel gas stream going to the loading rack flare).
* * * * *
(3) * * *
(iii) If the operation change results in a sulfur content that is
outside the range of concentrations included in the original
application and the owner or operator chooses not to submit new
information to support an exemption, the owner or operator must begin
H2S monitoring using daily stain sampling to demonstrate
compliance. The owner or operator must begin monitoring according to
the requirements in paragraphs (a)(1) or (a)(2) of this section as soon
as practicable, but in no case later than 180 days after the operation
change. During daily stain tube sampling, a daily sample exceeding 162
ppmv is an exceedance of the 3-hour H2S concentration limit.
The owner or operator of a fuel gas combustion device must also
determine a rolling 365-day average using the stain sampling results;
an average H2S concentration of 5 ppmv must be used for days
within the rolling 365-day period prior to the operation change.
(c) Process heaters complying with the NOX
concentration-based limit. The owner or operator of a process heater
subject to the NOX emissions limit in Sec. 60.102a(g)(2)
and electing to comply with the applicable emissions limit in Sec.
60.102a(g)(2)(i)(A), (g)(2)(ii)(A), (g)(2)(iii)(A) or (g)(2)(iv)(A)
shall install, operate, calibrate and maintain an instrument for
continuously monitoring and recording the concentration (dry basis, 0-
percent excess air) of NOX emissions into the atmosphere
according to the requirements in paragraphs (c)(1) through (5) of this
section, except as provided in paragraph (c)(6) of this section. The
monitor must include an O2 monitor for correcting the data
for excess air.
(1) Except as provided in paragraph (c)(6) of this section, the
owner or operator shall install, operate and maintain each
NOX monitor according to Performance Specification 2 of
Appendix B to part 60. The span value of this NOX monitor
must be between 2 and 3 times the applicable emissions limit,
inclusive.
* * * * *
(6) The owner or operator of a process heater that has a rated
heating capacity of less than 100 MMBtu and is equipped with combustion
modification-based technology to reduce NOX emissions (i.e.,
low-NOX burners, ultra-low-NOX burners) may elect
to comply with the monitoring requirements in paragraphs (c)(1) through
(5) of this section or, alternatively, the owner or operator of such a
process heater shall conduct biennial performance tests according to
the requirements in Sec. 60.104a(i), establish a maximum excess
O2 operating limit or operating curve according to the
requirements in Sec. 60.104a(i)(6) and comply with the O2
monitoring requirements in paragraphs (c)(3) through (5) of this
section to demonstrate compliance. If an O2 operating curve
is used (i.e., if different O2 operating limits are
established for different operating ranges), the owner or operator of
the process heater must also monitor fuel gas flow rate, fuel oil flow
rate (as applicable) and heating value content according to the methods
provided in paragraphs (d)(5), (d)(6), and (d)(4) or (d)(7) of this
section, respectively.
(d) Process heaters complying with the NOX heating
value-based or mass-based limit. The owner or operator of a process
heater subject to the NOX emissions limit in Sec.
60.102a(g)(2) and electing to comply with the applicable emissions
limit in Sec. 60.102a(g)(2)(i)(B) or (g)(2)(ii)(B) shall install,
operate, calibrate and maintain an instrument for continuously
monitoring and recording the concentration (dry basis, 0-percent excess
air) of NOX emissions into the
[[Page 56475]]
atmosphere and shall determine the F factor of the fuel gas stream no
less frequently than once per day according to the monitoring
requirements in paragraphs (d)(1) through (4) of this section. The
owner or operator of a co-fired process heater subject to the
NOX emissions limit in Sec. 60.102a(g)(2) and electing to
comply with the heating value-based limit in Sec.
60.102a(g)(2)(iii)(B) or (g)(2)(iv)(B) shall install, operate,
calibrate and maintain an instrument for continuously monitoring and
recording the concentration (dry basis, 0-percent excess air) of
NOX emissions into the atmosphere according to the
monitoring requirements in paragraph (d)(1) of this section; install,
operate, calibrate and maintain an instrument for continuously
monitoring and recording the flow rate of the fuel gas and fuel oil fed
to the process heater according to the monitoring requirements in
paragraph (d)(5) and (6) of this section; for fuel gas streams,
determine gas composition according to the requirements in paragraph
(d)(4) of this section or the higher heating value according to the
requirements in paragraph (d)(7) of this section; and for fuel oil
streams, determine the heating value according to the monitoring
requirements in paragraph (d)(7) of this section.
(1) Except as provided in paragraph (d)(8) of this section, the
owner or operator shall install, operate and maintain each
NOX monitor according to the requirements in paragraphs
(c)(1) through (5) of this section. The monitor must include an
O2 monitor for correcting the data for excess air.
(2) Except as provided in paragraph (d)(3) of this section, the
owner or operator shall sample and analyze each fuel stream fed to the
process heater using the methods and equations in section 12.3.2 of EPA
Method 19 of Appendix A-7 to part 60 to determine the F factor on a dry
basis. If a single fuel gas system provides fuel gas to several process
heaters, the F factor may be determined at a single location in the
fuel gas system provided it is representative of the fuel gas fed to
the affected process heater(s).
(3) As an alternative to the requirements in paragraph (d)(2) of
this section, the owner or operator of a gas-fired process heater shall
install, operate and maintain a gas composition analyzer and determine
the average F factor of the fuel gas using the factors in Table 1 of
this subpart and Equation 10 of this section. If a single fuel gas
system provides fuel gas to several process heaters, the F factor may
be determined at a single location in the fuel gas system provided it
is representative of the fuel gas fed to the affected process
heater(s).
[GRAPHIC] [TIFF OMITTED] TR12SE12.008
Where:
Fd = F factor on dry basis at 0-percent excess air, dscf/
MMBtu.
Xi = mole or volume fraction of each component in the
fuel gas.
MEVi = molar exhaust volume, dry standard cubic feet per
mole (dscf/mol).
MHCi = molar heat content, Btu per mole (Btu/mol).
1,000,000 = unit conversion, Btu per MMBtu.
(4) The owner or operator shall conduct performance evaluations of
each compositional monitor according to the requirements in Performance
Specification 9 of Appendix B to part 60. Any of the following methods
shall be used for conducting the relative accuracy evaluations:
(i) EPA Method 18 of Appendix A-6 to part 60;
(ii) ASTM D1945-03 (Reapproved 2010)(incorporated by reference-see
Sec. 60.17);
(iii) ASTM D1946-90 (Reapproved 2006)(incorporated by reference-see
Sec. 60.17);
(iv) ASTM D6420-99 (Reapproved 2004)(incorporated by reference-see
Sec. 60.17);
(v) GPA 2261-00 (incorporated by reference-see Sec. 60.17); or
(vi) ASTM UOP539-97 (incorporated by reference-see Sec. 60.17).
(5) The owner or operator shall install, operate and maintain fuel
gas flow monitors according to the manufacturer's recommendations. For
volumetric flow meters, temperature and pressure monitors must be
installed in conjunction with the flow meter or in a representative
location to correct the measured flow to standard conditions (i.e., 68
[deg]F and 1 atmosphere). For mass flow meters, use gas compositions
determined according to paragraph (d)(4) of this section to determine
the average molecular weight of the fuel gas and convert the mass flow
to a volumetric flow at standard conditions (i.e., 68 [deg]F and 1
atmosphere). The owner or operator shall conduct performance
evaluations of each fuel gas flow monitor according to the requirements
in Sec. 60.13 and Performance Specification 6 of Appendix B to part
60. Any of the following methods shall be used for conducting the
relative accuracy evaluations:
(i) EPA Method 2, 2A, 2B, 2C or 2D of Appendix A-2 to part 60;
(ii) ASME MFC-3M-2004 (incorporated by reference-see Sec. 60.17);
(iii) ANSI/ASME MFC-4M-1986 (Reaffirmed 2008) (incorporated by
reference-see Sec. 60.17);
(iv) ASME MFC-6M-1998 (Reaffirmed 2005) (incorporated by reference-
see Sec. 60.17);
(v) ASME/ANSI MFC-7M-1987 (Reaffirmed 2006) (incorporated by
reference-see Sec. 60.17);
(vi) ASME MFC-11M-2006 (incorporated by reference-see Sec. 60.17);
(vii) ASME MFC-14M-2003 (incorporated by reference-see Sec.
60.17);
(viii) ASME MFC-18M-2001 (incorporated by reference-see Sec.
60.17);
(ix) AGA Report No. 3, Part 1 (incorporated by reference-see Sec.
60.17);
(x) AGA Report No. 3, Part 2 (incorporated by reference-see Sec.
60.17);
(xi) AGA Report No. 11 (incorporated by reference-see Sec. 60.17);
(xii) AGA Report No. 7 (incorporated by reference-see Sec. 60.17);
and
(xiii) API Manual of Petroleum Measurement Standards, Chapter 22,
Section 2 (incorporated by reference-see Sec. 60.17).
(6) The owner or operator shall install, operate and maintain each
fuel oil flow monitor according to the manufacturer's recommendations.
The owner or operator shall conduct performance evaluations of each
fuel oil flow monitor according to the requirements in Sec. 60.13 and
Performance Specification 6 of Appendix B to part 60. Any of the
following methods shall be used for conducting the relative accuracy
evaluations:
(i) Any one of the methods listed in paragraph (d)(5) of this
section that are applicable to fuel oil (i.e., ``fluids'');
(ii) ANSI/ASME-MFC-5M-1985 (Reaffirmed 2006) (incorporated by
reference-see Sec. 60.17);
[[Page 56476]]
(iii) ASME/ANSI MFC-9M-1988 (Reaffirmed 2006) (incorporated by
reference-see Sec. 60.17);
(iv) ASME MFC-16-2007 (incorporated by reference-see Sec. 60.17);
(v) ASME MFC-22-2007 (incorporated by reference-see Sec. 60.17);
or
(vi) ISO 8316 (incorporated by reference-see Sec. 60.17).
(7) The owner or operator shall determine the higher heating value
of each fuel fed to the process heater using any of the applicable
methods included in paragraphs (d)(7)(i) through (ix) of this section.
If a common fuel supply system provides fuel gas or fuel oil to several
process heaters, the higher heating value of the fuel in each fuel
supply system may be determined at a single location in the fuel supply
system provided it is representative of the fuel fed to the affected
process heater(s). The higher heating value of each fuel fed to the
process heater must be determined no less frequently than once per day
except as provided in paragraph (d)(7)(x) of this section.
(i) ASTM D240-02 (Reapproved 2007) (incorporated by reference-see
Sec. 60.17).
(ii) ASTM D1826-94 (Reapproved 2003) (incorporated by reference-see
Sec. 60.17).
(iii) ASTM D1945-03 (Reapproved 2010) (incorporated by reference-
see Sec. 60.17).
(iv) ASTM D1946-90 (Reapproved 2006) (incorporated by reference-see
Sec. 60.17).
(v) ASTM D3588-98 (Reapproved 2003) (incorporated by reference-see
Sec. 60.17).
(vi) ASTM D4809-06 (incorporated by reference-see Sec. 60.17).
(vii) ASTM D4891-89 (Reapproved 2006) (incorporated by reference-
see Sec. 60.17).
(viii) GPA 2172-09 (incorporated by reference-see Sec. 60.17).
(ix) Any of the methods specified in section 2.2.7 of Appendix D to
part 75.
(x) If the fuel oil supplied to the affected co-fired process
heater originates from a single storage tank, the owner or operator may
elect to use the storage tank sampling method in section 2.2.4.2 of
Appendix D to part 75 instead of daily sampling, except that the most
recent value for heating content must be used.
(8) The owner or operator of a process heater that has a rated
heating capacity of less than 100 MMBtu and is equipped with combustion
modification based technology to reduce NOX emissions (i.e.,
low-NOX burners or ultra-low NOX burners) may
elect to comply with the monitoring requirements in paragraphs (d)(1)
through (7) of this section or, alternatively, the owner or operator of
such a process heater shall conduct biennial performance tests
according to the requirements in Sec. 60.104a(i), establish a maximum
excess O2 operating limit or operating curve according to
the requirements in Sec. 60.104a(i)(6) and comply with the
O2 monitoring requirements in paragraphs (c)(3) through (5)
of this section to demonstrate compliance. If an O2
operating curve is used (i.e., if different O2 operating
limits are established for different operating ranges), the owner or
operator of the process heater must also monitor fuel gas flow rate,
fuel oil flow rate (as applicable) and heating value content according
to the methods provided in paragraphs (d)(5), (d)(6), and (d)(4) or
(d)(7) of this section, respectively.
(e) Sulfur monitoring for assessing root cause analysis threshold
for affected flares. Except as described in paragraphs (e)(4) and (h)
of this section, the owner or operator of an affected flare subject to
Sec. 60.103a(c) through (e) shall determine the total reduced sulfur
concentration for each gas line directed to the affected flare in
accordance with either paragraph (e)(1), (e)(2) or (e)(3) of this
section. Different options may be elected for different gas lines. If a
monitoring system is in place that is capable of complying with the
requirements related to either paragraph (e)(1), (e)(2) or (e)(3) of
this section, the owner or operator of a modified flare must comply
with the requirements related to either paragraph (e)(1), (e)(2) or
(e)(3) of this section upon startup of the modified flare. If a
monitoring system is not in place that is capable of complying with the
requirements related to either paragraph (e)(1), (e)(2) or (e)(3) of
this section, the owner or operator of a modified flare must comply
with the requirements related to either paragraph (e)(1), (e)(2) or
(e)(3) of this section no later than November 11, 2015 or upon startup
of the modified flare, whichever is later.
(1) Total reduced sulfur monitoring requirements. The owner or
operator shall install, operate, calibrate and maintain an instrument
for continuously monitoring and recording the concentration of total
reduced sulfur in gas discharged to the flare.
(i) The owner or operator shall install, operate and maintain each
total reduced sulfur monitor according to Performance Specification 5
of Appendix B to part 60. The span value should be determined based on
the maximum sulfur content of gas that can be discharged to the flare
(e.g., roughly 1.1 to 1.3 times the maximum anticipated sulfur
concentration), but may be no less than 5,000 ppmv. A single dual range
monitor may be used to comply with the requirements of this paragraph
and paragraph (a)(2) of this section provided the applicable span
specifications are met.
(ii) The owner or operator shall conduct performance evaluations of
each total reduced sulfur monitor according to the requirements in
Sec. 60.13(c) and Performance Specification 5 of Appendix B to part
60. For flares that routinely have flow, the owner or operator of each
total reduced sulfur monitor shall use EPA Method 15A of Appendix A-5
to part 60 for conducting the relative accuracy evaluations. The method
ANSI/ASME PTC 19.10-1981 (incorporated by reference-see Sec. 60.17) is
an acceptable alternative to EPA Method 15A of Appendix A-5 to part 60.
The alternative relative accuracy procedures described in section 16.0
of Performance Specification 2 of Appendix B to part 60 (cylinder gas
audits) may be used for conducting the relative accuracy evaluations.
For flares that do not receive routine flow, the alternative relative
accuracy procedures described in section 16.0 of Performance
Specification 2 of Appendix B to part 60 (cylinder gas audits) may be
used for conducting the relative accuracy evaluations, except that it
is not necessary to include as much of the sampling probe or sampling
line as practical.
(iii) The owner or operator shall comply with the applicable
quality assurance procedures in Appendix F to part 60 for each total
reduced sulfur monitor.
(2) H2S monitoring requirements. The owner or operator
shall install, operate, calibrate, and maintain an instrument for
continuously monitoring and recording the concentration of
H2S in gas discharged to the flare according to the
requirements in paragraphs (e)(2)(i) through (iii) of this section and
shall collect and analyze samples of the gas and calculate total sulfur
concentrations as specified in paragraphs (e)(2)(iv) through (ix) of
this section.
(i) The owner or operator shall install, operate and maintain each
H2S monitor according to Performance Specification 7 of
Appendix B to part 60. The span value should be determined based on the
maximum sulfur content of gas that can be discharged to the flare
(e.g., roughly 1.1 to 1.3 times the maximum anticipated sulfur
concentration), but may be no less than 5,000 ppmv. A single dual range
H2S monitor may be used to comply with the requirements of
this paragraph and paragraph (a)(2) of
[[Page 56477]]
this section provided the applicable span specifications are met.
(ii) The owner or operator shall conduct performance evaluations of
each H2S monitor according to the requirements in Sec.
60.13(c) and Performance Specification 7 of Appendix B to part 60. For
flares that routinely have flow, the owner or operator shall use EPA
Method 11, 15 or 15A of Appendix A-5 to part 60 for conducting the
relative accuracy evaluations. The method ANSI/ASME PTC 19.10-1981
(incorporated by reference--see Sec. 60.17) is an acceptable
alternative to EPA Method 15A of Appendix A-5 to part 60. The
alternative relative accuracy procedures described in section 16.0 of
Performance Specification 2 of Appendix B to part 60 (cylinder gas
audits) may be used for conducting the relative accuracy evaluations.
For flares that do not receive routine flow, the alternative relative
accuracy procedures described in section 16.0 of Performance
Specification 2 of Appendix B to part 60 (cylinder gas audits) may be
used for conducting the relative accuracy evaluations, except that it
is not necessary to include as much of the sampling probe or sampling
line as practical.
(iii) The owner or operator shall comply with the applicable
quality assurance procedures in Appendix F to part 60 for each
H2S monitor.
(iv) In the first 10 operating days after the date the flare must
begin to comply with Sec. 60.103a(c)(1), the owner or operator shall
collect representative daily samples of the gas discharged to the
flare. The samples may be grab samples or integrated samples. The owner
or operator shall take subsequent representative daily samples at least
once per week or as required in paragraph (e)(2)(ix) of this section.
(v) The owner or operator shall analyze each daily sample for total
sulfur using either EPA Method 15A of Appendix A-5 to part 60, EPA
Method 16A of Appendix A-6 to part 60, ASTM Method D4468-85 (Reapproved
2006) (incorporated by reference--see Sec. 60.17) or ASTM Method
D5504-08 (incorporated by reference--see Sec. 60.17).
(vi) The owner or operator shall develop a 10-day average total
sulfur-to-H2S ratio and 95-percent confidence interval as
follows:
(A) Calculate the ratio of the total sulfur concentration to the
H2S concentration for each day during which samples are
collected.
(B) Determine the 10-day average total sulfur-to-H2S
ratio as the arithmetic average of the daily ratios calculated in
paragraph (e)(2)(vi)(A) of this section.
(C) Determine the acceptable range for subsequent weekly samples
based on the 95-percent confidence interval for the distribution of
daily ratios based on the 10 individual daily ratios using Equation 11
of this section.
[GRAPHIC] [TIFF OMITTED] TR12SE12.009
Where:
AR = Acceptable range of subsequent ratio determinations, unitless.
RatioAvg = 10-day average total sulfur-to-H2S
concentration ratio, unitless.
2.262 = t-distribution statistic for 95-percent 2-sided confidence
interval for 10 samples (9 degrees of freedom).
SDev = Standard deviation of the 10 daily average total sulfur-to-
H2S concentration ratios used to develop the 10-day
average total sulfur-to-H2S concentration ratio,
unitless.
(vii) For each day during the period when data are being collected
to develop a 10-day average, the owner or operator shall estimate the
total sulfur concentration using the measured total sulfur
concentration measured for that day.
(viii) For all days other than those during which data are being
collected to develop a 10-day average, the owner or operator shall
multiply the most recent 10-day average total sulfur-to-H2S
ratio by the daily average H2S concentrations obtained using
the monitor as required by paragraph (e)(2)(i) through (iii) of this
section to estimate total sulfur concentrations.
(ix) If the total sulfur-to-H2S ratio for a subsequent
weekly sample is outside the acceptable range for the most recent
distribution of daily ratios, the owner or operator shall develop a new
10-day average ratio and acceptable range based on data for the
outlying weekly sample plus data collected over the following 9
operating days.
(3) SO2 monitoring requirements. The owner or operator
shall install, operate, calibrate and maintain an instrument for
continuously monitoring and recording the concentration of
SO2 from a process heater or other fuel gas combustion
device that is combusting gas representative of the fuel gas in the
flare gas line according to the requirements in paragraph (a)(1) of
this section, determine the F factor of the fuel gas at least daily
according to the requirements in paragraphs (d)(2) through (4) of this
section, determine the higher heating value of the fuel gas at least
daily according to the requirements in paragraph (d)(7) of this section
and calculate the total sulfur content (as SO2) in the fuel
gas using Equation 12 of this section.
[GRAPHIC] [TIFF OMITTED] TR12SE12.010
Where:
TSFG = Total sulfur concentration, as SO2, in
the fuel gas, ppmv.
CSO2 = Concentration of SO2 in the exhaust
gas, ppmv (dry basis at 0-percent excess air).
Fd = F factor gas on dry basis at 0-percent excess air,
dscf/MMBtu.
HHVFG = Higher heating value of the fuel gas, MMBtu/scf.
(4) Exemptions from sulfur monitoring requirements. Flares
identified in paragraphs (e)(4)(i) through (iv) of this section are
exempt from the requirements in paragraphs (e)(1) through (3) of this
section. For each such flare, except as provided in paragraph
(e)(4)(iv), engineering calculations shall be used to calculate the
SO2 emissions in the event of a discharge that may trigger a
root cause analysis under Sec. 60.103a(c)(1).
(i) Flares that can only receive:
(A) Fuel gas streams that are inherently low in sulfur content as
described in paragraph (a)(3)(i) through (iv) of this section; and/or
(B) Fuel gas streams that are inherently low in sulfur content for
which the owner or operator has applied for an exemption from the
H2S monitoring requirements as described in paragraph (b) of
this section.
(ii) Emergency flares, provided that for each such flare, the owner
or operator complies with the monitoring alternative in paragraph (g)
of this section.
[[Page 56478]]
(iii) Flares equipped with flare gas recovery systems designed,
sized and operated to capture all flows except those resulting from
startup, shutdown or malfunction, provided that for each such flare,
the owner or operator complies with the monitoring alternative in
paragraph (g) of this section.
(iv) Secondary flares that receive gas diverted from the primary
flare. In the event of a discharge from the secondary flare, the sulfur
content measured by the sulfur monitor on the primary flare should be
used to calculate SO2 emissions, regardless of whether or
not the monitoring alternative in paragraph (g) of this section is
selected for the secondary flare.
(f) Flow monitoring for flares. Except as provided in paragraphs
(f)(2) and (h) of this section, the owner or operator of an affected
flare subject to Sec. 60.103a(c) through (e) shall install, operate,
calibrate and maintain, in accordance with the specifications in
paragraph (f)(1) of this section, a CPMS to measure and record the flow
rate of gas discharged to the flare. If a flow monitor is not already
in place, the owner or operator of a modified flare shall comply with
the requirements of this paragraph by no later than November 11, 2015
or upon startup of the modified flare, whichever is later.
(1) The owner or operator shall install, calibrate, operate and
maintain each flow monitor according to the manufacturer's procedures
and specifications and the following requirements.
(i) Locate the monitor in a position that provides a representative
measurement of the total gas flow rate.
(ii) Use a flow sensor with a measurement sensitivity of no more
than 5 percent of the flow rate or 10 cubic feet per minute, whichever
is greater.
(iii) Use a flow monitor that is maintainable online, is able to
continuously correct for temperature and pressure and is able to record
flow in standard conditions (as defined in Sec. 60.2) over one-minute
averages.
(iv) At least quarterly, perform a visual inspection of all
components of the monitor for physical and operational integrity and
all electrical connections for oxidation and galvanic corrosion if the
flow monitor is not equipped with a redundant flow sensor.
(v) Recalibrate the flow monitor in accordance with the
manufacturer's procedures and specifications biennially (every two
years) or at the frequency specified by the manufacturer.
(2) Emergency flares, secondary flares and flares equipped with
flare gas recovery systems designed, sized and operated to capture all
flows except those resulting from startup, shutdown or malfunction are
not required to install continuous flow monitors; provided, however,
that for any such flare, the owner or operator shall comply with the
monitoring alternative in paragraph (g) of this section.
(g) Alternative monitoring for certain flares equipped with water
seals. The owner or operator of an affected flare subject to Sec.
60.103a(c) through (e) that can be classified as either an emergency
flare, a secondary flare or a flare equipped with a flare gas recovery
system designed, sized and operated to capture all flows except those
resulting from startup, shutdown or malfunction may, as an alternative
to the sulfur and flow monitoring requirements of paragraphs (e) and
(f) of this section, install, operate, calibrate and maintain, in
accordance with the requirements in paragraphs (g)(1) through (7) of
this section, a CPMS to measure and record the pressure in the flare
gas header between the knock-out pot and water seal and to measure and
record the water seal liquid level. If the required monitoring systems
are not already in place, the owner or operator of a modified flare
shall comply with the requirements of this paragraph by no later than
November 11, 2015 or upon startup of the modified flare, whichever is
later.
(1) Locate the pressure sensor(s) in a position that provides a
representative measurement of the pressure and locate the liquid seal
level monitor in a position that provides a representative measurement
of the water column height.
(2) Minimize or eliminate pulsating pressure, vibration and
internal and external corrosion.
(3) Use a pressure sensor and level monitor with a minimum
tolerance of 1.27 centimeters of water.
(4) Using a manometer, check pressure sensor calibration quarterly.
(5) Conduct calibration checks any time the pressure sensor exceeds
the manufacturer's specified maximum operating pressure range or
install a new pressure sensor.
(6) In a cascaded flare system that employs multiple secondary
flares, pressure and liquid level monitoring is required only on the
first secondary flare in the system (i.e., the secondary flare with the
lowest pressure release set point).
(7) This alternative monitoring option may be elected only for
flares with four or fewer pressure exceedances required to be reported
under Sec. 60.108a(d)(5) (``reportable pressure exceedances'') in any
365 consecutive calendar days. Following the fifth reportable pressure
exceedance in a 365-day period, the owner or operator must comply with
the sulfur and flow monitoring requirements of paragraphs (e) and (f)
of this section as soon as practical, but no later than 180 days after
the fifth reportable pressure exceedance in a 365-day period.
(h) Alternative monitoring for flares located in the BAAQMD or
SCAQMD. An affected flare subject to this subpart located in the BAAQMD
may elect to comply with the monitoring requirements in both BAAQMD
Regulation 12, Rule 11 and BAAQMD Regulation 12, Rule 12 as an
alternative to complying with the requirements of paragraphs (e) and
(f) of this section. An affected flare subject to this subpart located
in the SCAQMD may elect to comply with the monitoring requirements in
SCAQMD Rule 1118 as an alternative to complying with the requirements
of paragraphs (e) and (f) of this section.
(i) Excess emissions. For the purpose of reports required by Sec.
60.7(c), periods of excess emissions for fuel gas combustion devices
subject to the emissions limitations in Sec. 60.102a(g) and flares
subject to the concentration requirement in Sec. 60.103a(h) are
defined as specified in paragraphs (i)(1) through (5) of this section.
Determine a rolling 3-hour or a rolling daily average as the arithmetic
average of the applicable 1-hour averages (e.g., a rolling 3-hour
average is the arithmetic average of three contiguous 1-hour averages).
Determine a rolling 30-day or a rolling 365-day average as the
arithmetic average of the applicable daily averages (e.g., a rolling
30-day average is the arithmetic average of 30 contiguous daily
averages).
(1) SO 2 or H2S limits for fuel gas combustion devices. (i) If the
owner or operator of a fuel gas combustion device elects to comply with
the SO2 emission limits in Sec. 60.102a(g)(1)(i), each
rolling 3-hour period during which the average concentration of
SO2 as measured by the SO2 continuous monitoring
system required under paragraph (a)(1) of this section exceeds 20 ppmv,
and each rolling 365-day period during which the average concentration
of SO2 as measured by the SO2 continuous
monitoring system required under paragraph (a)(1) of this section
exceeds 8 ppmv.
(ii) If the owner or operator of a fuel gas combustion device
elects to comply with the H2S concentration limits in Sec.
60.102a(g)(1)(ii), each rolling 3-hour period during which the average
concentration of H2S as measured by the
[[Page 56479]]
H2S continuous monitoring system required under paragraph
(a)(2) of this section exceeds 162 ppmv and each rolling 365-day period
during which the average concentration as measured by the
H2S continuous monitoring system under paragraph (a)(2) of
this section exceeds 60 ppmv.
(iii) If the owner or operator of a fuel gas combustion device
becomes subject to the requirements of daily stain tube sampling in
paragraph (b)(3)(iii) of this section, each day during which the daily
concentration of H2S exceeds 162 ppmv and each rolling 365-
day period during which the average concentration of H2S
exceeds 60 ppmv.
(2) H2S concentration limits for flares. (i) Each
rolling 3-hour period during which the average concentration of
H2S as measured by the H2S continuous monitoring
system required under paragraph (a)(2) of this section exceeds 162
ppmv.
(ii) If the owner or operator of a flare becomes subject to the
requirements of daily stain tube sampling in paragraph (b)(3)(iii) of
this section, each day during which the daily concentration of
H2S exceeds 162 ppmv.
(3) Rolling 30-day average NOX limits for fuel gas
combustion devices. Each rolling 30-day period during which the average
concentration of NOX as measured by the NOX
continuous monitoring system required under paragraph (c) or (d) of
this section exceeds:
(i) For a natural draft process heater, 40 ppmv and, if monitored
according to Sec. 60.107a(d), 0.040 lb/MMBtu;
(ii) For a forced draft process heater, 60 ppmv and, if monitored
according to Sec. 60.107a(d), 0.060 lb/MMBtu; and
(iii) For a co-fired process heater electing to comply with the
NOX limit in Sec. 60.102a(g)(2)(iii)(A) or (g)(2)(iv)(A),
150 ppmv.
(iv) The site-specific limit determined by the Administrator under
Sec. 60.102a(i).
(4) Daily NOX limits for fuel gas combustion devices.
Each day during which the concentration of NOX as measured
by the NOX continuous monitoring system required under
paragraph (d) of this section exceeds the daily average emissions limit
calculated using Equation 3 in Sec. 60.102a(g)(2)(iii)(B) or Equation
4 in Sec. 60.102a(g)(2)(iv)(B).
(5) Daily O2 limits for fuel gas combustion devices.
Each day during which the concentration of O2 as measured by
the O2 continuous monitoring system required under paragraph
(c)(6) of this section exceeds the O2 operating limit or
operating curve determined during the most recent biennial performance
test.
0
18. Section 60.108a is amended by:
0
a. Revising paragraph (b);
0
b. Revising paragraph (c)(1);
0
c. Revising paragraph (c)(6) introductory text and paragraphs
(c)(6)(ii) through (vi);
0
d. Adding paragraphs (c)(6)(vii), (viii), (ix), (x) and (xi);
0
e. Adding paragraph (c)(7); and
0
f. Revising paragraph (d)(5).
The revisions and additions read as follows:
Sec. 60.108a Recordkeeping and reporting requirements.
* * * * *
(b) Each owner or operator subject to an emissions limitation in
Sec. 60.102a shall notify the Administrator of the specific monitoring
provisions of Sec. Sec. 60.105a, 60.106a and 60.107a with which the
owner or operator intends to comply. Each owner or operator of a co-
fired process heater subject to an emissions limitation in Sec.
60.102a(g)(2)(iii) or (iv) shall submit to the Administrator
documentation showing that the process heater meets the definition of a
co-fired process heater in Sec. 60.101a. Notifications required by
this paragraph shall be submitted with the notification of initial
startup required by Sec. 60.7(a)(3).
(c) * * *
(1) A copy of the flare management plan.
* * * * *
(6) Records of discharges greater than 500 lb SO2 in any
24-hour period from any affected flare, discharges greater than 500 lb
SO2 in excess of the allowable limits from a fuel gas
combustion device or sulfur recovery plant and discharges to an
affected flare in excess of 500,000 scf above baseline in any 24-hour
period as required by Sec. 60.103a(c). If the monitoring alternative
provided in Sec. 60.107a(g) is selected, the owner or operator shall
record any instance when the flare gas line pressure exceeds the water
seal liquid depth, except for periods attributable to compressor
staging that do not exceed the staging time specified in Sec.
60.103a(a)(3)(vii)(C). The following information shall be recorded no
later than 45 days following the end of a discharge exceeding the
thresholds:
* * * * *
(ii) The date and time the discharge was first identified and the
duration of the discharge.
(iii) The measured or calculated cumulative quantity of gas
discharged over the discharge duration. If the discharge duration
exceeds 24 hours, record the discharge quantity for each 24-hour
period. For a flare, record the measured or calculated cumulative
quantity of gas discharged to the flare over the discharge duration. If
the discharge duration exceeds 24 hours, record the quantity of gas
discharged to the flare for each 24-hour period. Engineering
calculations are allowed for fuel gas combustion devices, but are not
allowed for flares, except for those complying with the alternative
monitoring requirements in Sec. 60.107a(g).
(iv) For each discharge greater than 500 lb SO2 in any
24-hour period from a flare, the measured total sulfur concentration or
both the measured H2S concentration and the estimated total
sulfur concentration in the fuel gas at a representative location in
the flare inlet.
(v) For each discharge greater than 500 lb SO2 in excess
of the applicable short-term emissions limit in Sec. 60.102a(g)(1)
from a fuel gas combustion device, either the measured concentration of
H2S in the fuel gas or the measured concentration of
SO2 in the stream discharged to the atmosphere. Process
knowledge can be used to make these estimates for fuel gas combustion
devices, but cannot be used to make these estimates for flares, except
as provided in Sec. 60.107a(e)(4).
(vi) For each discharge greater than 500 lb SO2 in
excess of the allowable limits from a sulfur recovery plant, either the
measured concentration of reduced sulfur or SO2 discharged
to the atmosphere.
(vii) For each discharge greater than 500 lb SO2 in any
24-hour period from any affected flare or discharge greater than 500 lb
SO2 in excess of the allowable limits from a fuel gas
combustion device or sulfur recovery plant, the cumulative quantity of
H2S and SO2 released into the atmosphere. For
releases controlled by flares, assume 99-percent conversion of reduced
sulfur or total sulfur to SO2. For fuel gas combustion
devices, assume 99-percent conversion of H2S to
SO2.
(viii) The steps that the owner or operator took to limit the
emissions during the discharge.
(ix) The root cause analysis and corrective action analysis
conducted as required in Sec. 60.103a(d), including an identification
of the affected facility, the date and duration of the discharge, a
statement noting whether the discharge resulted from the same root
cause(s) identified in a previous analysis and either a description of
the recommended corrective action(s) or an explanation of why
corrective action is not necessary under Sec. 60.103a(e).
(x) For any corrective action analysis for which corrective actions
are required in Sec. 60.103a(e), a description of the corrective
action(s) completed within the first 45 days following the discharge
[[Page 56480]]
and, for action(s) not already completed, a schedule for
implementation, including proposed commencement and completion dates.
(xi) For each discharge from any affected flare that is the result
of a planned startup or shutdown of a refinery process unit or
ancillary equipment connected to the affected flare, a statement that a
root cause analysis and corrective action analysis are not necessary
because the owner or operator followed the flare management plan.
(7) If the owner or operator elects to comply with Sec.
60.107a(e)(2) for a flare, records of the H2S and total
sulfur analyses of each grab or integrated sample, the calculated daily
total sulfur-to-H2S ratios, the calculated 10-day average
total sulfur-to-H2S ratios and the 95-percent confidence
intervals for each 10-day average total sulfur-to-H2S ratio.
(d) * * *
(5) The information described in paragraph (c)(6) of this section
for all discharges listed in paragraph (c)(6) of this section. For a
flare complying with the monitoring alternative under Sec. 60.107a(g),
following the fifth discharge required to be recorded under paragraph
(c)(6) of this section and reported under this paragraph, the owner or
operator shall include notification that monitoring systems will be
installed according to Sec. 60.107a(e) and (f) within 180 days
following the fifth discharge.
* * * * *
0
19. Section 60.109a is amended by revising paragraph (b) introductory
text and adding paragraph (b)(4) to read as follows:
Sec. 60.109a Delegation of authority.
* * * * *
(b) In delegating implementation and enforcement authority of this
subpart to a state, local or tribal agency, the approval authorities
contained in paragraphs (b)(1) through (4) of this section are retained
by the Administrator of the U.S. EPA and are not transferred to the
state, local or tribal agency.
* * * * *
(4) Approval of an application for an alternative means of emission
limitation under Sec. 60.103a(j) of this subpart.
0
20. Table 1 to subpart Ja is added to read as follows:
Table 1 to subpart Ja of Part 60--Molar Exhaust Volumes and Molar Heat
Content of Fuel Gas Constituents
------------------------------------------------------------------------
MEV\a\ MHC\b\
Constituent dscf/mol Btu/mol
------------------------------------------------------------------------
Methane (CH4)..................................... 7.29 842
Ethane (C2H6)..................................... 12.96 1,475
Hydrogen (H2)..................................... 1.61 269
Ethene (C2H4)..................................... 11.34 1,335
Propane (C3H8).................................... 18.62 2,100
Propene (C3H6).................................... 17.02 1,947
Butane (C4H10).................................... 24.30 2,717
Butene (C4H8)..................................... 22.69 2,558
Inerts............................................ 0.85 0
------------------------------------------------------------------------
\a\ MEV = molar exhaust volume, dry standard cubic feet per gram-mole
(dscf/g-mol) at standard conditions of 68[emsp14][deg]F and 1
atmosphere.
\b\ MHC = molar heat content (higher heating value basis), Btu per gram-
mole (Btu/g-mol).
[FR Doc. 2012-20866 Filed 9-11-12; 8:45 am]
BILLING CODE 6560-50-P