National Emissions Standards for Hazardous Air Pollutants: Ferroalloys Production, 37365-37401 [2015-15038]
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Vol. 80
Tuesday,
No. 125
June 30, 2015
Part II
Environmental Protection Agency
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40 CFR Part 63
National Emissions Standards for Hazardous Air Pollutants: Ferroalloys
Production; Final Rule
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Federal Register / Vol. 80, No. 125 / Tuesday, June 30, 2015 / Rules and Regulations
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 63
[EPA–HQ–OAR–2010–0895; FRL–9928–66–
OAR]
RIN 2060–AQ11
National Emissions Standards for
Hazardous Air Pollutants: Ferroalloys
Production
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
This action finalizes the
residual risk and technology review
(RTR) conducted for the Ferroalloys
Production source category regulated
under national emission standards for
hazardous air pollutants (NESHAP).
These final amendments include
revisions to particulate matter (PM)
standards for electric arc furnaces, metal
oxygen refining processes, and crushing
and screening operations, and expand
and revise the requirements to control
process fugitive emissions from furnace
operations, tapping, casting, and other
processes. We are also finalizing opacity
limits, as proposed in 2014. However,
regarding opacity monitoring, in lieu of
Method 9, we are requiring monitoring
with the digital camera opacity
technique (DCOT). Furthermore, we are
finalizing emissions standards for four
previously unregulated hazardous air
pollutants (HAP): Formaldehyde,
hydrogen chloride (HCl), mercury (Hg)
and polycyclic aromatic hydrocarbons
(PAH). Other requirements related to
testing, monitoring, notification,
recordkeeping, and reporting are
included. This rule is health protective
due to the revised emissions limits for
the stacks and the requirement of
enhanced fugitive emissions controls
that will achieve significant reductions
of process fugitive emissions, especially
manganese.
DATES: This final action is effective on
June 30, 2015. The incorporation by
reference of certain publications listed
in the rule is approved by the Director
of the Federal Register as of June 30,
2015.
ADDRESSES: The Environmental
Protection Agency (EPA) has established
a docket for this action under Docket ID
No. EPA–HQ–OAR–2010–0895. All
documents in the docket are listed on
the www.regulations.gov Web site.
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.
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SUMMARY:
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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 through
https://www.regulations.gov, or in hard
copy at the EPA Docket Center, EPA
WJC West Building, Room Number
3334, 1301 Constitution Ave. NW.,
Washington, DC. The Public Reading
Room hours of operation are 8:30 a.m.
to 4:30 p.m. Eastern Standard Time
(EST), Monday through Friday. 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: For
questions about this final action, contact
Phil Mulrine, Sector Policies and
Programs Division (D243–02), Office of
Air Quality Planning and Standards,
U.S. Environmental Protection Agency,
Research Triangle Park, North Carolina,
27711; telephone number: (919) 541–
5289; fax number: (919) 541–3207; and
email address: mulrine.phil@epa.gov.
For specific information regarding the
risk modeling methodology, contact
Darcie Smith, Health and
Environmental Impacts Division (C539–
02), Office of Air Quality Planning and
Standards, U.S. Environmental
Protection Agency, Research Triangle
Park, North Carolina 27711; telephone
number: (919) 541–2076; fax number:
(919) 541–0840; and email address:
smith.darcie@epa.gov. For information
about the applicability of the NESHAP
to a particular entity, contact Cary
Secrest, Office of Enforcement and
Compliance Assurance, U.S.
Environmental Protection Agency, EPA
WJC Building, 1200 Pennsylvania Ave.
NW., Washington, DC 20460; telephone
number: (202) 564–8661; and email
address: secrest.cary@epa.gov.
SUPPLEMENTARY INFORMATION:
Preamble Acronyms and Abbreviation
We use multiple acronyms and terms
in this preamble. While this list may not
be exhaustive, to ease the reading of this
preamble and for reference purposes,
the EPA defines the following terms and
acronyms here:
ATSDR Agency for Toxic Substances and
Disease Registry
BLDS bag leak detection system
BTF Beyond-the-Floor
CAA Clean Air Act
CBI Confidential Business Information
CFR Code of Federal Regulations
EJ environmental justice
EPA Environmental Protection Agency
ERPG Emergency Response Planning
Guidelines
ERT Electronic Reporting Tool
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FeMn Ferromanganese
FR Federal Register
HAP hazardous air pollutants
HCl hydrochloric acid
HI Hazard Index
HQ Hazard Quotient
ICR Information Collection Request
IRIS Integrated Risk Information System
km kilometer
MACT maximum achievable control
technology
mg/dscm milligrams per dry standard cubic
meter
mg/m3 milligrams per cubic meter
MIR maximum individual risk
MOR metal oxygen refining
MRL Minimal Risk Level
NAAQS National Ambient Air Quality
Standards
NAICS North American Industry
Classification System
NESHAP National Emissions Standards for
Hazardous Air Pollutants
NTTAA National Technology Transfer and
Advancement Act
OAQPS Office of Air Quality Planning and
Standards
OECA Office of Enforcement and
Compliance Assurance
OMB Office of Management and Budget
PAH polycyclic aromatic hydrocarbons
PB–HAP hazardous air pollutants known to
be persistent and bio-accumulative in the
environment
PM particulate matter
POM polycyclic organic matter
REL reference exposure level
RFA Regulatory Flexibility Act
RfC reference concentration
RTR residual risk and technology review
SAB Science Advisory Board
SBA Small Business Administration
SiMn Silicomanganese
SSM startup, shutdown, and malfunction
TOSHI target organ-specific hazard index
TPY tons per year
TRIM.FaTE Total Risk Integrated
Methodology.Fate, Transport, and
Ecological Exposure model
TTN Technology Transfer Network
mg/dscm micrograms per dry standard cubic
meter
mg/m3 micrograms per cubic meter
UMRA Unfunded Mandates Reform Act
UPL Upper Prediction Limit
VCS voluntary consensus standards
Background Information
On November 23, 2011, and October
6, 2014, the EPA proposed revisions to
the Ferroalloys Production NESHAP
based on our RTR. In this action, we are
finalizing decisions and revisions for
the NESHAP. We summarize some of
the more significant comments we
timely received regarding the proposed
rule and provide our responses in this
preamble. A summary of all other public
comments on the proposal and the
EPA’s responses to those comments are
available in document titled: National
Emission Standards for Hazardous Air
Pollutant Emissions: Ferroalloys
Production Summary of Public
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Comments and the EPA’s Responses on
Proposed Rule (76 FR 72508, November
23, 2011) and Supplemental Proposal
(79 FR 60238, October 6, 2014), Docket
ID No. EPA–HQ–OAR–2010–0895,
which is available in the docket. A
‘‘track changes’’ version of the
regulatory language that incorporates
the changes in this action is also
available in the docket.
Organization of this Document. The
information in this preamble is
organized as follows:
I. General Information
A. Does this action apply to me?
B. Where can I get a copy of this document
and other related information?
C. Judicial Review and Administrative
Reconsideration
II. Background
A. What is the statutory authority for this
action?
B. What is the Ferroalloys Production
source category and how does the
NESHAP regulate HAP emissions from
the source category?
C. What changes did we propose for the
Ferroalloys Production source category
in our November 23, 2011, proposal and
our October 6, 2014, supplemental
proposal?
III. What is included in this final rule?
A. What are the final rule amendments
based on the risk review for the
Ferroalloys Production source category?
B. What are the final rule amendments
based on the technology review for the
Ferroalloys Production source category?
C. What are the final rule amendments
pursuant to CAA section 112(d)(2) & (3)
for the Ferroalloys Production source
category?
D. What are requirements during periods of
startup, shutdown, and malfunction?
E. What other changes have been made to
the NESHAP?
F. What are the effective and compliance
dates of the standards?
G. What are the requirements for
submission of performance test data to
the EPA?
IV. What is the rationale for our final
decisions and amendments for the
Ferroalloys Production source category?
A. Residual Risk Review for the Ferroalloys
Production Source Category
B. Technology Review for the Ferroalloys
Production Source Category
C. CAA Section 112(d)(2) & (3) Revisions
for the Ferroalloys Production Source
Category
D. What changes did we make to the
Ferroalloys Production opacity
monitoring requirement?
V. Summary of Cost, Environmental, and
Economic Impacts and Additional
Analyses Conducted
A. What are the affected sources?
B. What are the air quality impacts?
C. What are the cost impacts?
D. What are the economic impacts?
E. What are the benefits?
F. What analysis of environmental justice
did we conduct?
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G. What analysis of children’s
environmental health did we conduct?
VI. Statutory and Executive Order Reviews
A. Executive Orders 12866: Regulatory
Planning and Review and Executive
Order 13563: Improving Regulation and
Regulatory Review
B. Paperwork Reduction Act (PRA)
C. Regulatory Flexibility Act (RFA)
D. Unfunded Mandates Reform Act
(UMRA)
E. Executive Order 13132: Federalism
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
G. Executive Order 13045: Protection of
Children From Environmental Health
Risks and Safety Risks
H. Executive Order 13211: Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution or Use
I. National Technology Transfer and
Advancement Act and 1 CFR part 51
J. Executive Order 12898: Federal Actions
To Address Environmental Justice in
Minority Populations and Low-Income
Populations
K. Congressional Review Act (CRA)
I. General Information
A. Does this action apply to me?
Regulated Entities. Categories and
entities potentially regulated by this
action are shown in Table 1 of this
preamble.
TABLE 1—NESHAP AND INDUSTRIAL
SOURCE CATEGORIES AFFECTED BY
THIS FINAL ACTION
NESHAP and source category
NAICS a
Code
Ferroalloys Production ..............
331112
a North
American
Industry
Classification
System.
Table 1 of this preamble is not
intended to be exhaustive, but rather to
provide a guide for readers regarding
entities likely to be affected by the final
action for the source category listed. To
determine whether your facility is
affected, you should examine the
applicability criteria in 40 CFR part 63,
subpart XXX (National Emission
Standards for Hazardous Air Pollutants
(NESHAP): Ferroalloys Production). If
you have any questions regarding the
applicability of any aspect of this
NESHAP, please contact the appropriate
person listed in the preceding FOR
FURTHER INFORMATION CONTACT section of
this preamble.
B. Where can I get a copy of this
document and other related
information?
In addition to being available in the
docket, an electronic copy of this final
action will also be available on the
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Internet through the Technology
Transfer Network (TTN) Web site, a
forum for information and technology
exchange in various areas of air
pollution control. Following signature
by the EPA Administrator, the EPA will
post a copy of this final action at:
https://www.epa.gov/ttn/atw/ferroa/
ferropg.html. Following publication in
the Federal Register, the EPA will post
the Federal Register version and key
technical documents at this same Web
site.
Additional information is available on
the RTR Web site at https://
www.epa.gov/ttn/atw/rrisk/rtrpg.html.
This information includes an overview
of the RTR program, links to project
Web sites for the RTR source categories
and detailed emissions and other data
we used as inputs to the risk
assessments.
C. Judicial Review and Administrative
Reconsideration
Under CAA section 307(b)(1), judicial
review of this final action is available
only by filing a petition for review in
the United States Court of Appeals for
the District of Columbia Circuit by
August 31, 2015. Under CAA section
307(b)(2), the requirements established
by this final rule may not be challenged
separately in any civil or criminal
proceedings brought by the EPA to
enforce the requirements.
Section 307(d)(7)(B) of the Clean Air
Act (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 the EPA to reconsider the rule ‘‘[i]f
the person raising an objection can
demonstrate to the Administrator 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
should submit a Petition for
Reconsideration to the Office of the
Administrator, U.S. EPA, Room 3000,
EPA WJC 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.
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II. Background
A. What is the statutory authority for
this action?
Section 112 of the CAA establishes a
two-stage regulatory process to address
emissions of HAP from stationary
sources. In the first stage, we must
identify categories of sources emitting
one or more of the HAP listed in CAA
section 112(b) and then promulgate
technology-based NESHAP for those
sources. ‘‘Major sources’’ are those that
emit, or have the potential to emit, any
single HAP at a rate of 10 tons per year
(tpy) or more, or 25 tpy or more of any
combination of HAP. For major sources,
these standards are commonly referred
to as maximum achievable control
technology (MACT) standards and must
reflect the maximum degree of emission
reductions of HAP achievable (after
considering cost, energy requirements,
and non-air quality health and
environmental impacts). In developing
MACT standards, CAA section 112(d)(2)
directs the EPA to consider the
application of measures, processes,
methods, systems, or techniques,
including, but not limited to those that
reduce the volume of or eliminate HAP
emissions through process changes,
substitution of materials, or other
modifications; enclose systems or
processes to eliminate emissions;
collect, capture, or treat HAP when
released from a process, stack, storage,
or fugitive emissions point; are design,
equipment, work practice, or
operational standards; or any
combination of the above.
For these MACT standards, the statute
specifies certain minimum stringency
requirements, which are referred to as
MACT floor requirements, and which
may not be based on cost
considerations. See CAA section
112(d)(3). For new sources, the MACT
floor cannot be less stringent than the
emission control achieved in practice by
the best-controlled similar source. For
existing sources the MACT standards
can be less stringent than the floors for
new sources, but they cannot be less
stringent than the average emission
limitation achieved by the bestperforming 12 percent of existing
sources in the category or subcategory
(or the best-performing five sources for
categories or subcategories with fewer
than 30 sources). In developing MACT
standards, we must also consider
control options that are more stringent
than the floor, under CAA section
112(d)(2). We may establish standards
more stringent than the floor, based on
the consideration of the cost of
achieving the emissions reductions, any
non-air quality health and
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environmental impacts, and energy
requirements.
In the second stage of the regulatory
process, the CAA requires the EPA to
undertake two different analyses, which
we refer to as the technology review and
the residual risk review. Under the
technology review, we must review the
technology-based standards and revise
them ‘‘as necessary (taking into account
developments in practices, processes,
and control technologies)’’ no less
frequently than every 8 years, pursuant
to CAA section 112(d)(6). Under the
residual risk review, we must evaluate
the risk to public health remaining after
application of the technology-based
standards and revise the standards, if
necessary, to provide an ample margin
of safety to protect public health or to
prevent, taking into consideration costs,
energy, safety, and other relevant
factors, an adverse environmental effect.
The residual risk review is required
within 8 years after promulgation of the
technology-based standards, pursuant to
CAA section 112(f). In conducting the
residual risk review, if the EPA
determines that the current standards
provide an ample margin of safety to
protect public health, it is not necessary
to revise the MACT standards pursuant
to CAA section 112(f).1 For more
information on the statutory authority
for this rule, see 79 FR 60238.
B. What is the Ferroalloys Production
source category and how does the
NESHAP regulate HAP emissions from
the source category?
The EPA promulgated the Ferroalloys
Production NESHAP on May 20, 1999
(64 FR 27450). The standards are
codified at 40 CFR part 63, subpart
XXX. The ferroalloys production
industry consists of facilities that
produce ferromanganese (FeMn) or
silicomanganese (SiMn). The source
category covered by this MACT
standard currently includes two
facilities.
The rule applies to ferroalloys
production operations that are located at
major sources of HAP emissions or are
co-located at a major source of HAP
emissions. The HAP emission sources at
facilities subject to the Ferroalloys
Production NESHAP are open, semisealed, or sealed submerged arc
furnaces, tapping operations, casting
operations, metal oxygen refining
1 The U.S. Court of Appeals has affirmed this
approach of implementing CAA section
112(f)(2)(A); NRDC v. EPA, 529 F.3d 1077, 1083
(D.C. Cir. 2008) (‘‘If EPA determines that the
existing technology-based standards provide an
‘ample margin of safety,’ then the Agency is free to
readopt those standards during the residual risk
rulemaking.’’).
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(MOR) process, crushing and screening
operations, other processes, such as
ladle treatment and slag raking, and
outdoor fugitive dust sources. The 1999
NESHAP regulated these emissions
sources through emission limits for PM,
opacity limits, and work practices.
C. What changes did we propose for the
Ferroalloys Production source category
in our November 23, 2011, proposal and
our October 6, 2014, supplemental
proposal?
On November 23, 2011, the EPA
published a proposed rule in the
Federal Register (76 FR 72508) for the
Ferroalloys Production NESHAP, 40
CFR part 63, subpart XXX that took into
consideration the RTR analyses. In the
2011 proposed rule, we proposed:
• Revisions to the numeric emission
limits for PM from furnace stacks to
reflect the current performance of
control devices in place at ferroalloys
production facilities to control furnace
emissions (primary and tapping),
crushing and screening operations, and
the MOR operation at one plant;
• Addition of Hg, HCl, PAH, and
formaldehyde furnace stack emission
standards that reflected the MACT
determination for control of these
pollutants;
• Requirements to capture process
fugitive emissions using full building
enclosure with negative pressure
building ventilation and duct the
captured emissions to a control device;
and
• Revisions to the opacity standards
to reflect effective capture and control of
process fugitive emissions.
On October 6, 2014, the EPA
published a supplemental proposed rule
in the Federal Register (79 FR 60238).
For the supplemental proposal, we
proposed:
• Revisions to the proposed PM
furnace stack emission standards based
on additional test data submitted by the
facilities;
• Revisions to the proposed Hg, HCl,
and PAH furnace stack emission
standards based on additional test data
submitted by the facilities;
• Requirements to capture process
fugitive emissions using effective,
enhanced local capture, and duct the
captured emissions to control devices;
• Revisions to the opacity standards
to reflect effective, enhanced capture,
and control of process fugitive
emissions;
• To demonstrate compliance with
the opacity limits, we proposed
facilities would need to take opacity
readings for an entire furnace cycle once
per week per furnace using Method 9 or
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as an option they could take the
readings using DCOT; and
• Several minor clarifications and
corrections.
III. What is included in this final rule?
This action finalizes the EPA’s
determinations pursuant to the RTR
provisions of CAA section 112 for the
Ferroalloys Production source category
and amends the existing Ferroalloys
Production NESHAP based on those
determinations. Among the changes
finalized in this action are: The
promulgation of MACT-based limits for
previously unregulated HAP;
requirements to effectively capture and
control process fugitive emissions; the
removal of startup, shutdown, and
malfunction (SSM) exemptions; and the
addition of DCOT monitoring. This
action also reflects several changes to
the November 2011 and October 2014
proposals in consideration of comments
received during the public comment
periods as described in section IV of this
preamble.
A. What are the final rule amendments
based on the risk review for the
Ferroalloys Production source category?
This section provides a summary of
the final amendments to the Ferroalloys
Production NESHAP being promulgated
pursuant to CAA section 112(f).
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1. Stack Emissions
We are promulgating PM emission
limits for stacks at the following levels:
4.0 milligrams per dry standard cubic
meter (mg/dscm) for new or
reconstructed electric arc furnaces; 25
mg/dscm for existing electric arc
furnaces; and 4.0 mg/dscm for any new,
reconstructed, or existing local
ventilation control device. These
emission limits are the same as the
limits proposed in the 2014
supplemental proposal.
In addition, we are promulgating a
PM limit of 3.9 mg/dscm for any new,
reconstructed, or existing MOR process
and a PM limit of 13 mg/dscm for any
new, reconstructed, or existing crushing
and screening equipment, which are
consistent with what we proposed in
our November 23, 2011, proposal.
2. Process Fugitive Emissions Sources
We are promulgating a requirement
that facilities in this source category
must achieve effective enhanced capture
of process fugitive emissions using a
system of primary hoods (that capture
process fugitive emissions near the
source) and/or secondary capture of
fugitives (which would capture
remaining fugitive emissions near the
roof-line). Facilities must install,
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operate, and maintain a process
fugitives capture system that is designed
to capture 95 percent or more of the
process fugitive emissions. We are also
promulgating an opacity limit of 8percent to ensure process fugitive
emissions are effectively captured. This
is what we proposed in the October 6,
2014, supplemental proposal. However,
we have revised the rule based on
public comment, to provide more
flexibility on how facilities achieve 95percent capture of process fugitive
emissions. We also strengthened the
monitoring provisions to ensure that the
required reductions are achieved.
B. What are the final rule amendments
based on the technology review for the
Ferroalloys Production source category?
We determined that there are
developments in practices, processes,
and control technologies that warrant
revisions to the MACT standards for this
source category for both stack PM
emissions and process fugitive
emissions. Therefore, under the
authority of CAA section 112(d)(6), we
are promulgating the same PM stack
emission limits and enhanced fugitive
control requirements that we are
promulgating under CAA section 112(f),
as described in section A above.
C. What are the final rule amendments
pursuant to CAA section 112(d)(2) & (3)
for the Ferroalloys Production source
category?
We are promulgating emission limits
for formaldehyde, HCl, Hg, and PAH,
which were previously unregulated
HAP, pursuant to CAA section 112(d)(2)
and 112(d)(3).
We are promulgating a formaldehyde
emission limit of 201 micrograms per
dry standard cubic meter (mg/dscm) for
any new, reconstructed, or existing
electric arc furnace. This is the same
limit that we proposed on November 23,
2011.
We are promulgating an HCl emission
limit of 180 mg/dscm for new or
reconstructed electric arc furnaces and
1,100 mg/dscm for existing electric arc
furnaces. This is the same limit that we
proposed on October 6, 2014.
For electric arc furnaces producing
FeMn, we are promulgating Hg emission
limits of 13 mg/dscm for new or
reconstructed electric arc furnaces and
130 mg/dscm for existing electric arc
furnaces. For electric arc furnaces
producing SiMn, we are promulgating
Hg emission limits of 4 mg/dscm for new
or reconstructed electric arc furnaces
and 12 mg/dscm for existing electric arc
furnaces. The Hg limit for new SiMn
furnaces is the same as in the October
6, 2014, supplemental proposal. The
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final Hg limits for new and existing
FeMn and existing SiMn furnaces are
generally consistent with the
supplemental proposal; however, there
were changes to these three limits due
to the inclusion of new emission data
we received shortly before or during the
supplemental proposal comment period.
For electric arc furnaces producing
FeMn, we are promulgating a PAH
emission limit of 12,000 mg/dscm for
new or reconstructed and existing
electric arc furnaces. The FeMn furnace
PAH emission limits are significantly
higher than what we proposed in the
October 6, 2014, supplemental proposal
due to the inclusion of new PAH
emission data we received a few weeks
before signature of the supplemental
proposal and during the supplemental
proposal comment period. We
explained in the supplemental proposal
preamble that we received data shortly
before that notice and provided the data
for comment (i.e., the data were
available in the docket). The data
received during the comment period
were consistent with the data
mentioned in the supplemental
proposal. For electric arc furnaces
producing SiMn, we are promulgating a
PAH emission limit of 72 mg/dscm for
new or reconstructed electric arc
furnaces and 130 mg/dscm for existing
electric arc furnaces. The SiMn furnace
new PAH emission limit is the same as
the limit in the October 6, 2014,
supplemental proposal. There was a
slight revision to the existing SiMn
furnace PAH limit due to the inclusion
of new emission data we received
during the supplemental proposal
comment period.
D. What are the requirements during
periods of startup, shutdown and
malfunction?
We are finalizing, as proposed in the
supplemental proposal, changes to the
Ferroalloys Production NESHAP to
eliminate the SSM exemption.
Consistent with Sierra Club v. EPA 551
F. 3d 1019 (D.C. Cir. 2008), the EPA is
establishing standards in this rule that
apply at all times. Table 1 to subpart
XXX of part 63 (General Provisions
applicability table) is being revised to
change several references related to
requirements that apply during periods
of SSM. We also are eliminating or
revising certain recordkeeping and
reporting requirements related to the
eliminated SSM exemption. The EPA
also made changes to the rule to remove
or modify inappropriate, unnecessary,
or redundant language in the absence of
the SSM exemption. We determined
that facilities in this source category can
meet the applicable emission standards
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in the Ferroalloys Production NESHAP
at all times, including periods of startup
and shutdown; therefore, the EPA
determined that no separate standards
are needed to address emissions during
these periods.
E. What other changes have been made
to the NESHAP?
This rule also finalizes revisions to
several other Ferroalloys Production
NESHAP requirements as proposed, or
in some cases with some modification
as described in this section.
To increase the ease and efficiency of
data submittal and data accessibility, we
are finalizing, as proposed, a
requirement that owners and operators
of ferroalloys production facilities
submit electronic copies of certain
required performance test reports
through an electronic performance test
report tool called the Electronic
Reporting Tool (ERT). This requirement
to submit performance test data
electronically to the EPA does not
require any additional performance
testing and applies only to those
performance tests conducted using test
methods that are supported by the ERT.
We are finalizing the opacity
standards, as proposed in the
supplemental proposal. However,
regarding compliance demonstration,
we are requiring that facilities measure
opacity using DCOT. In the
supplemental proposal, we proposed
facilities would need to monitor opacity
with Method 9 or DCOT. However, after
considering public comments, we
decided to require DCOT rather than
have it as optional. Regarding
monitoring frequency, we proposed
facilities would need to do opacity
readings weekly per furnace building
with no opportunity to reduce
frequency overtime. After considering
public comments, we have decided to
require weekly readings initially, as
proposed, but allow a facility an
opportunity to decrease frequency of
opacity readings to monthly per furnace
building after 26 weeks of successful,
compliant opacity readings.
In addition, due to the large variation
in PAH emissions from furnace stacks
during FeMn production, we are
requiring quarterly compliance tests for
PAHs (i.e., four PAH compliance tests
per year) for furnaces while producing
FeMn, with an opportunity for facilities
to request decreased frequency of such
compliance testing from their permit
authority after the first year and after
four or more successful PAH
compliance tests have been completed
and submitted electronically.
We are also finalizing other minor
changes to the NESHAP in response to
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comments received during the public
comment period for the proposal and
supplemental proposal, as described in
this preamble.
F. What are the effective and
compliance dates of the standards?
The revisions to the MACT standards
being promulgated in this action are
effective on June 30, 2015. The
compliance date for existing ferroalloys
production sources for all the
requirements promulgated in this final
rule is June 30, 2017. Facilities must
comply with the changes set out in this
final rule (which are being promulgated
under CAA sections 112(d)(2), 112(d)(3),
112(d)(6), and 112(f)(2) for all affected
sources) no later than 2 years after the
effective date of the final rule. CAA
section 112(f)(4) generally provides that
a standard promulgated pursuant to
CAA section 112(f)(2) applies 90 days
after the effective date, but further
provides for a compliance period of up
to 2 years when the Administrator
determines that such time is necessary
for the installation of controls and that
steps will be taken during that period to
assure protection to health from
imminent endangerment. We conclude
that 2 years are necessary to complete
the installation of the enhanced local
capture system and other controls. In
the period between the effective date of
this rule and the compliance date,
existing sources will need to continue to
comply with the requirements specified
in 40 CFR 63.1650 through 40 CFR
63.1660. New sources must comply with
the all of the standards immediately
upon the effective date of the standard,
June 30, 2015, or upon startup,
whichever is later.
G. What are the requirements for
submission of performance test data to
the EPA?
As we proposed, the EPA is taking a
step to increase the ease and efficiency
of data submittal and data accessibility.
Specifically, the EPA is finalizing the
requirement for owners and operators of
ferroalloys production facilities to
submit electronic copies of certain
required performance test reports.
Data will be collected by direct
computer-to-computer electronic
transfer using EPA-provided software.
This EPA-provided software is an
electronic performance test report tool
called the ERT. The ERT will generate
an electronic report package which will
be submitted to the Compliance and
Emissions Data Reporting Interface
(CEDRI) and then archived to the EPA’s
Central Data Exchange (CDX). A
description and instructions for use of
the ERT can be found at https://
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www.epa.gov/ttn/chief/ert/
and CEDRI can be accessed through the
CDX Web site (https://www.epa.gov/cdx).
The requirement to submit
performance test data electronically to
the EPA does not create any additional
performance testing and will apply only
to those performance tests conducted
using test methods that are supported by
the ERT. A listing of the pollutants and
test methods supported by the ERT is
available at the ERT Web site. The EPA
believes, through this approach,
industry will save time in the
performance test submittal process.
Additionally, this rulemaking benefits
industry by reducing recordkeeping
costs as the performance test reports
that are submitted to the EPA using
CEDRI are no longer required to be kept
in hard copy.
State, local, and tribal agencies will
benefit from more streamlined and
accurate review of performance test data
that will become available through
WebFIRE. The public will also benefit.
Having these data publicly available
enhances transparency and
accountability. For a more thorough
discussion of electronic reporting of
performance tests using direct
computer-to-computer electronic
transfer and using EPA-provided
software, see the discussion in the
preamble of the proposal.
In summary, in addition to supporting
regulation development, control strategy
development, and other air pollution
control activities, having an electronic
database populated with performance
test data will save industry, state, local,
tribal agencies, and the EPA significant
time, money, and effort while improving
the quality of emission inventories and
air quality regulations and enhancing
the public’s access to this important
information.
IV. What is the rationale for our final
decisions and amendments for the
Ferroalloys Production source
category?
For each issue, this section provides
a description of what we proposed and
what we are finalizing for the issue, the
EPA’s rationale for the final decisions
and amendments, and a summary of key
comments and responses. For all
comments not discussed in this
preamble, comment summaries and the
EPA’s responses can be found in the
comment summary and response
document, which is available in the
docket.
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A. Residual Risk Review for the
Ferroalloys Production Source Category
1. What did we propose pursuant to
CAA section 112(f) for the Ferroalloys
Production source category?
Pursuant to CAA section 112(f), we
conducted a residual risk review and
presented the results of this review,
along with our proposed decisions
regarding risk acceptability and ample
margin of safety, in the October 6, 2014,
supplemental proposal for the
Ferroalloys Production NESHAP (79 FR
60238). The results of the risk
assessment for the 2014 supplemental
proposal are presented briefly below in
Table 2 and in more detail in the
residual risk document, Residual Risk
Assessment for the Ferroalloys Source
Category in Support of the September
2014 Supplemental Proposal, which is
available in the docket for this
rulemaking.
Based on actual emissions estimates
for the Ferroalloys Production source
category supplemental proposal, the
maximum individual risk (MIR) for
cancer was estimated to be up to 20-in1 million driven by emissions of
chromium compounds, PAHs, and
nickel compounds. The maximum
chronic non-cancer target organ-specific
hazard index (TOSHI) value was
estimated to be up to 4 driven by
fugitive emissions of manganese. The
maximum off-site acute hazard quotient
(HQ) value was estimated to be 1 for
arsenic compounds, hydrogen fluoride
(HF), and formaldehyde. The total
estimated national cancer incidence
from this source category, based on
actual emission levels, was 0.002 excess
cancer cases per year, or one case in
every 500 years.
Based on MACT-allowable emissions
estimated for the Ferroalloys Production
source category supplemental proposal,
the MIR was estimated to be up to 100in-1 million driven by emissions of
arsenic and cadmium compounds from
the MOR process baghouse outlet. The
maximum chronic non-cancer TOSHI
value was estimated to be up to 40
driven by emissions of manganese from
the MOR process. The total estimated
national cancer incidence from this
source category, based on MACTallowable emission levels, was 0.005
excess cancer cases per year, or one case
in every 200 years.
We also found there were emissions
of four persistent and bioaccumulative
HAP (PB–HAP) with an available RTR
multipathway screening value, and the
reported emissions of these four HAP
(cadmium compounds, dioxins/furans,
Hg compounds, and PAH) were greater
than the Tier 1 multipathway screening
values for these compounds for both
facilities at the time of the supplemental
proposal. We conducted a Tier 2
multipathway screen for both facilities,
and conducted a refined multipathway
assessment for one facility in the source
category. Results of the refined
multipathway assessment predict a
potential lifetime cancer risk of 10-in-1
million to the maximum exposed
individual due to exposure to dioxins
and PAHs. The non-cancer HQ was
predicted to be below 1 for cadmium
compounds and 1 for Hg compounds.
However, as explained in the Revised
Development of the Risk and
Technology Review (RTR) Emissions
Dataset for the Ferroalloys Production
Source Category for the 2014
Supplemental Proposal document, it is
37371
important to note that about 75 percent
of the emissions test results for dioxins
were below the detection limit. To be
conservative, in our calculations of
emissions estimates, we assumed all the
test results that were recorded as below
detection were one half the detection
limit. Therefore, there are considerable
uncertainties in estimated emissions for
dioxins. Nevertheless, since we
assumed emissions were at the level of
one half the detection limit in all these
cases where emissions were not even
detected, we believe our emissions
estimates are conservative (i.e., more
likely to be overestimates rather than
underestimates of the true emissions).
Emissions of the four PB–HAP and
two environmental HAP (HCl and HF)
were reported by ferroalloys facilities.
Tier 1 results for PB–HAP indicate that
concentrations of cadmium compounds
and dioxins are below the ecological
benchmarks. Mercury compounds and
PAHs concentrations were greater than
the benchmark so a Tier 2 screen was
conducted. For PAH and
methylmercury, none of the individual
modeled concentrations for any facility
exceeded any of the ecological
benchmarks. For mercuric chloride, the
weighted average modeled
concentrations for all soil parcels were
well below the soil benchmarks. For
HCl and HF, the average modeled
concentrations around each facility did
not exceed any ecological benchmarks.
For the supplemental proposal, we
weighed all health risk factors in our
risk acceptability determination and we
proposed that the residual risks from the
Ferroalloys Production source category
are unacceptable.
TABLE 2—FERROALLOYS INHALATION RISK ASSESSMENT RESULTS IN THE OCTOBER 2014 SUPPLEMENTAL PROPOSAL
Maximum individual cancer
risk (in 1 million) a
Maximum chronic
non-cancer TOSHI b
Actual
emissions
level
MACTallowable
emissions
level c
Estimated population at increased risk levels of cancer
Estimated annual
cancer incidence
(cases per year)
20 .................
100
>= 1-in-1 million: 31,000 ......
>= 10-in-1 million: 400 .........
>= 100-in-1 million: 0 ...........
0.002
Actual
emissions
level
MACTallowable
emissions
level
4
40
Maximum screening acute
non-cancer HQ d
HQREL = 1 (arsenic compounds, formaldehyde,
hydrofluoric acid).
a Estimated
maximum individual excess lifetime cancer risk due to HAP emissions from the source category.
TOSHI. The target organ with the highest TOSHI for the Ferroalloys Production source category for both actual and allowable
emissions is the neurological system. The estimated population at increased levels of noncancer hazard is 1,500 based on actual emissions and
11,000 based on allowable emissions.
c The development of allowable emission estimates can be found in the memorandum titled Revised Development of the RTR Emissions
Dataset for the Ferroalloys Production Source Category for the 2014 Supplemental Proposal, which is available in the docket.
d See section III.A.3 of the supplemental proposal or the risk assessment document supporting the supplemental proposal for explanation of
acute dose-response values. Acute assessments are not performed on allowable emissions.
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b Maximum
As described above, to address the
unacceptable risks in the supplemental
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proposal, we proposed tighter PM
emission limits for the stacks, which
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significantly reduce risks due to
allowable emissions. To reduce risks
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due to process fugitive emissions, we
proposed facilities must achieve
effective enhanced capture of process
fugitive emissions using a system of
primary hoods (that capture process
fugitive emissions near the source) and/
or secondary capture of fugitives (which
would capture remaining fugitive
emissions near the roof-line). As
described in the supplemental proposal,
we estimated that these controls would
reduce the MIR cancer risk estimate to
10-in-1 million and that the chronic
noncancer hazard index (HI) would be
reduced to an HI of 1. Acute screening
and multipathway results were also
reduced. In the supplemental proposal,
we concluded that these risks, after the
implementation of proposed controls,
were acceptable.
We then considered whether the
Ferroalloys Production NESHAP
provides an ample margin of safety to
protect public health and whether more
stringent standards are necessary to
prevent an adverse environmental
effect, taking into consideration costs,
energy, safety, and other relevant
factors. In considering whether the
standards should be tightened to
provide an ample margin of safety to
protect public health, we considered the
same risk factors that we considered for
our acceptability determination and also
considered the costs, technological
feasibility, and other relevant factors
related to emissions control options that
might reduce risks associated with
emissions from the source category.
Based on our ample margin of safety
analysis for the supplemental proposal,
we did not identify any additional costeffective controls to further reduce risks
beyond the requirements we proposed
to achieve acceptable risks. Therefore,
we proposed that additional HAP
emissions controls are not necessary to
provide an ample margin of safety.
Based on the results of our screening
analysis for risks to the environment, we
also proposed that more stringent
standards are not necessary to prevent
an adverse environmental effect.
2. How did the risk review change for
the Ferroalloys Production source
category?
Information received by the EPA
shortly before and during the
supplemental proposal comment period
included additional PAH and Hg test
data that were not included in the
supplemental proposal risk assessment
due to timing and the need to review the
data. We described the data in the
supplemental proposal and asked for
comment on the use of these data. After
completion of the data review, these
data were included in the risk
assessment for the final rule. Therefore,
PAH and Hg emissions estimates were
revised for the final rule assessment.
Some revisions were also made for other
HAP emissions. These changes are
discussed further in section IV of this
preamble.
With the exception of the revised
emissions described above, the risk
assessment supporting the final rule was
conducted in the same manner, using
the same models and methods, as that
conducted for the supplemental
proposal. The documentation for the
final rule risk assessment can be found
in the document titled Residual Risk
Assessment for the Ferroalloys Source
Category in Support of the 2015 Risk
and Technology Review Final Rule,
which is available in the docket for this
rulemaking.
a. Inhalation Risk Assessment Results.
Table 3 provides an overall summary of
the results of the inhalation risk
assessment supporting the final rule.
TABLE 3—FERROALLOYS INHALATION RISK ASSESSMENT RESULTS IN THE 2015 FINAL RULE
Maximum individual cancer
risk (in 1 million) a
Maximum chronic
non-cancer TOSHI b
Actual
emissions
level
MACTallowable
emissions
level c
Estimated population at increased risk levels of cancer
Estimated annual
cancer incidence
(cases per year)
20 .................
100
>= 1-in-1 million: 41,000 ......
>= 10-in-1 million: 90 ...........
>= 100-in-1 million: 0 ...........
0.003
Actual
emissions
level
MACTallowable
emissions
level
Maximum screening acute
non-cancer HQ d
4
40
HQREL = 1 (hydrofluoric
acid, arsenic compounds).
a Estimated
maximum individual excess lifetime cancer risk due to HAP emissions from the source category.
TOSHI. The target organ with the highest TOSHI for the Ferroalloys Production source category for both actual and allowable
emissions is the neurological system. The estimated population at increased levels of noncancer hazard is 1,300 based on actual emissions and
11,000 based on allowable emissions.
c The development of allowable emission estimates can be found in the memorandum titled Revised Development of the RTR Emissions
Dataset for the Ferroalloys Production Source Category for the 2014 Supplemental Proposal, which is available in the docket.
d See section III.A.3 of the supplemental proposal or the risk assessment document supporting the supplemental proposal for explanation of
acute dose-response values. Acute assessments are not performed on allowable emissions.
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b Maximum
The inhalation risk modeling
performed to estimate risks based on
actual and allowable emissions for the
final rule relied primarily on updated
emissions estimates based on data
received through two Information
Collection Requests (ICRs), additional
data submitted by the companies
voluntarily, and revised calculations as
described further in the Revised
Development of the Risk and
Technology Review (RTR) Emissions
Dataset for the Ferroalloys Production
Source Category for the 2015 Final Rule,
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which is available in the docket for this
action.
The results of the chronic baseline
inhalation cancer risk assessment
indicate that, based on updated
estimates of actual emissions, the cancer
MIR posed by the Ferroalloys
Production source category is 20-in-1
million, with chromium compounds,
PAHs, and nickel compounds from
tapping fugitives, furnace fugitives, and
furnace stacks accounting for more than
70 percent of the MIR. The total
estimated cancer incidence from
ferroalloys production sources based on
updated actual emission levels is 0.003
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excess cancer cases per year, or one case
every 333 years, with emissions of PAH,
chromium compounds, and cadmium
compounds contributing 49 percent, 15
percent, and 12 percent, respectively, to
this cancer incidence. In addition, we
note that approximately 90 people are
estimated to have cancer risks greater
than or equal to 10-in-1 million, and
approximately 41,000 people are
estimated to have risks greater than or
equal to 1-in-1 million because of actual
emissions from this source category.
These results, based on updated actual
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emissions, are very similar to those
presented in the supplemental proposal.
When considering the updated
MACT-allowable emissions, the
maximum individual lifetime cancer
risk is estimated to be up to 100-in-1
million, driven by emissions of arsenic
and cadmium compounds from the
MOR process baghouse outlet. The
estimated cancer incidence is estimated
to be 0.006 excess cancer cases per year
or one excess case in every 167 years.
Approximately 3,300 people are
estimated to have cancer risks greater
than or equal to 10-in-1 million and
approximately 120,000 people are
estimated to have cancer risks greater
than or equal to 1-in-1 million
considering updated allowable
emissions from ferroalloys facilities.
These results, based on updated MACTallowable emissions, are very similar to
those presented in the supplemental
proposal.
The maximum modeled chronic noncancer HI (TOSHI) value for the source
category based on updated actual
emissions is estimated to be 4, with
manganese emissions from tapping
fugitives accounting for more than 50
percent of the HI. Approximately 1,300
people are estimated to have exposure
to HI levels greater than 1 as a result of
updated actual emissions from this
source category. When considering
updated MACT-allowable emissions,
the maximum chronic non-cancer
TOSHI is estimated to be 40, driven by
manganese emissions from the MOR
process baghouse outlet. Approximately
12,000 people are estimated to have
potential exposure to TOSHI levels
greater than 1 considering updated
allowable emissions from these
ferroalloys facilities. These results, for
both updated actual and MACTallowable emissions, are very similar to
those presented in the supplemental
proposal.
b. Acute Risk Results. Based on the
updated emissions described above, our
screening analysis for worst-case acute
impacts based on actual emissions
indicates the potential for hydrofluoric
acid and arsenic compounds to have HQ
results of 1, based on their respective
REL values. Both facilities have
estimated acute HQs of 1 for these
pollutants. Acute HQs for other
pollutants (e.g., hydrochloric acid) are
less than one. These acute results, based
on updated emissions, are very similar
to those presented in the supplemental
proposal.
All the HAP in this analysis have
worst-case acute HQ values of 1 or less,
indicating that they carry no potential to
pose acute concerns. In characterizing
the potential for acute non-cancer
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impacts of concern, it is important to
remember the upward bias of these
exposure estimates (e.g., worst-case
meteorology coinciding with a person
located at the point of maximum
concentration during the hour) and to
consider the results along with the
conservative estimates used to develop
peak hourly emissions as described
earlier, as well as the screening
methodology. More discussion of our
acute screening methods can be found
in the supplemental proposal or in the
risk assessment document, Residual
Risk Assessment for the Ferroalloys
Production Source Category in Support
of the 2015 Final Rule, which are
available in the docket.
c. Multipathway Risk Screening
Results. Results of the worst-case Tier I
screening analysis indicate that PB–
HAP emissions (based on updated
estimates of actual emissions) from one
or both facilities in this source category
exceed the screening emission rates for
cadmium compounds, Hg compounds,
dioxins, and PAHs. For the compounds
and facilities that did not screen out at
Tier I, we conducted a Tier II screen.
Based on the Tier II screening
analysis, no facility emits cadmium
compounds above the Tier II screening
levels. One facility emits Hg compounds
above the Tier II screening levels and
exceeds that level by a factor of 8. Both
facilities emit chlorinated
dibenzodioxins and furans (CDDF) as
2,3,7,8-tetrachlorodibenzo-p-dioxin
toxicity equivalent (TEQ) above the Tier
II screening levels and the facility with
the highest emissions of dioxins exceeds
its Tier II screening level by a factor of
10. Both facilities emit POM as
benzo(a)pyrene TEQ above the Tier II
screening levels and the facility with the
highest emissions exceeds its screening
level by a factor of 50. These
multipathway screening results, based
on updated emissions, are very similar
to those presented in the supplemental
proposal. More information about our
multipathway screening approach can
be found in the supplemental proposal
or in the risk assessment document,
Residual Risk Assessment for the
Ferroalloys Production Source Category
in Support of the 2015 Final Rule,
which are available in the docket.
d. Multipathway Refined Risk Results.
A refined multipathway analysis was
conducted for one of the two facilities
in this source category using the
TRIM.FaTE model and the updated
emissions as described above. The
facility, Eramet Marietta Incorporated,
in Marietta, Ohio, was selected based
upon its close proximity to nearby lakes,
and farms as well as having the highest
potential multipathway risks for three of
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37373
the four PB–HAP based on the Tier II
analysis. In addition, it was selected for
a refined multipathway assessment in
the supplemental proposal. These three
PB–HAP were cadmium, Hg, and PAHs.
Even though neither facility exceeded
the Tier II screening levels for cadmium,
Eramet had the higher value. Eramet
also emits dioxins, but the other facility
had a higher exceedance of its Tier II
screening level. The refined analysis
was conducted on all four PB–HAP
using updated emissions as described
above. The refined analysis for this
facility showed that the Tier II screen
for each pollutant over-predicted the
potential risk when compared to the
refined analysis results.
Overall, the refined analysis predicts
a potential lifetime cancer risk of 20-in1 million to the maximum most exposed
individual due to exposure to dioxins
and PAHs. The non-cancer HQ is
predicted to be below 1 for cadmium
compounds and 1 for Hg compounds.
These results, based on updated
emissions, are very similar to those
presented in the supplemental proposal.
Further details on the refined
multipathway analysis can be found in
Appendix 10 of the Residual Risk
Assessment for the Ferroalloys
Production Source Category in Support
of the 2015 Final Rule, which is
available in the docket.
e. Environmental Risk Screening
Results. As described in section III.A of
the supplemental proposal preamble
(79 FR 60238), we conducted an
environmental risk screening
assessment for the Ferroalloys
Production source category. In the Tier
I screening analysis for PB–HAP (other
than lead, which was evaluated
differently as noted in section III.A of
the supplemental proposal preamble, 79
FR 60238), the individual modeled Tier
I concentrations for one facility in the
source category exceeded some
sediment, fish-avian piscivorus, and
surface soil benchmarks for PAHs,
methylmercury, and mercuric chloride.
Therefore, we conducted a Tier II
assessment.
In the Tier II screening analysis for
PAHs and methylmercury, none of the
individual modeled concentrations for
any facility in the source category
exceeded any of the ecological
benchmarks (either the lowest-observedadverse-effect level or the no-observedadverse-effect level). For mercuric
chloride, soil benchmarks were
exceeded for some individual modeled
points that collectively accounted for 11
percent of the modeled area. However,
the weighted average modeled
concentration for all soil parcels was
well below the soil benchmarks. For
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lead, we did not estimate any
exceedances of the secondary lead
National Ambient Air Quality Standards
(NAAQS).
For HCl, each individual
concentration (i.e., each off-site data
point in the modeling domain) was
below the ecological benchmarks for all
facilities. The average modeled HCl
concentration around each facility (i.e.,
the average concentration of all off-site
data points in the modeling domain) did
not exceed any ecological benchmark.
For HF, some individual modeled
points exceeded the ecological
benchmark but accounted for less than
0.02 percent of the modeled area. The
average modeled HF concentration
around each facility (i.e., the average
concentration of all off-site data points
in the modeling domain) did not exceed
any ecological benchmarks. These
results, based on updated emissions, are
very similar to those presented in the
supplemental proposal.
f. Facility-Wide Risk Assessment
Results. As in the supplemental
proposal, for both facilities in this
source category, there are no other HAP
emissions sources present beyond those
included in the source category.
Therefore, we conclude that the facilitywide risk is the same as the source
category risk and that no separate
facility-wide analysis is necessary.
g. Demographic Analysis Results. To
examine the potential for any
environmental justice (EJ) issues that
might be associated with the source
category, we updated the demographic
analysis that was conducted for the
supplemental proposal, using the risk
results based on the updated emissions.
A demographic analysis is an
assessment of risks to individual
demographic groups of the population
close to the facilities. In this analysis,
we evaluated the distribution of HAPrelated cancer risks and noncancer
hazards from the Ferroalloys Production
source category across different social,
demographic, and economic groups
within the populations living near
facilities identified as having the highest
risks. The methodology and the results
of the demographic analyses are
included in a technical report, Risk and
Technology Review—Analysis of SocioEconomic Factors for Populations Living
Near Ferroalloys Facilities, which is
available in the docket for this action.
The results of the demographic
analysis are summarized in Table 4
below. These results, for various
demographic groups, are based on the
estimated risks from actual emissions
levels for the population living within
50 kilometers (km) of the facilities.
TABLE 4—FERROALLOYS PRODUCTION DEMOGRAPHIC RISK ANALYSIS RESULTS FOR 2015 FINAL RULE
Population with
cancer risk at or
above 1-in-1
million due to
Ferroalloys
Production
Nationwide
Total Population .........................................................................................................
Population with
chronic hazard
index above 1 due
to Ferroalloys
Production
312,861,265
40,748
1,348
72
28
97
3
99
1
72
13
1
14
97
1
0
2
99
0
0
1
17
83
1
99
1
99
14
86
15
85
6
94
15
85
11
89
10
90
24
63
13
21
61
18
22
59
19
Race by Percent
White ..........................................................................................................................
All Other Races .........................................................................................................
Race by Percent
White ..........................................................................................................................
African American .......................................................................................................
Native American ........................................................................................................
Other and Multiracial .................................................................................................
Ethnicity by Percent
Hispanic .....................................................................................................................
Non-Hispanic .............................................................................................................
Income by Percent
Below Poverty Level ..................................................................................................
Above Poverty Level ..................................................................................................
Education by Percent
Over 25 and without High School Diploma ...............................................................
Over 25 and with a High School Diploma .................................................................
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Age by Percent
Ages 0 to 17 ..............................................................................................................
Ages 18 to 64 ............................................................................................................
Ages 65 and up .........................................................................................................
The results of the Ferroalloys
Production source category
demographic analysis indicate that
emissions from the source category
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expose approximately 41,000 people to
a cancer risk at or above 1-in-1 million
and approximately 1,300 people to a
chronic non-cancer TOSHI greater than
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1 (we note that many of those in the first
risk group are the same as those in the
second). The percentages of the at-risk
population in each demographic group
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(except for ages 65 and up) are similar
to or lower than their respective
nationwide percentages. These results
are very similar to those presented in
the supplemental proposal.
3. What key comments did we receive
on the risk review, and what are our
responses?
Several comments were received
regarding the risk assessment for the
Ferroalloys Production source category.
The following is a summary of some of
the more significant comments and our
responses to those comments. Other
comments received and our responses to
those comments can be found in the
document titled National Emission
Standards for Hazardous Air Pollutant
Emissions: Ferroalloys Production
Summary of Public Comments and the
EPA’s Responses on Proposed Rule (76
FR 72508, November 23, 2011) and
Supplemental Proposal (79 FR 60238,
October 6, 2014), which is available in
the docket for this action (EPA–HQ–
OAR–2010–0895).
Comment: Several comments were
received on the reference value used in
the risk assessment to evaluate chronic
noncancer effects due to exposure to
manganese. In the 2011 proposal, we
used the Integrated Risk Information
System (IRIS) reference concentration
(RfC), and we received negative
comments regarding that value not
being the ‘‘best available science.’’ We
evaluated the available values and, in
accordance with our prioritized doseresponse values and Scientific Advisory
Board (SAB) comments, we used the
Agency for Toxic Substances and
Disease Registry (ATSDR) minimum risk
level (MRL) for manganese in the risk
assessment for the 2014 supplemental
proposal. We received mixed comments
in response to the supplemental
proposal. Some comments were
negative regarding our use of the
ATSDR MRL, while others were
generally supportive of our use of the
MRL compared to the IRIS value, yet
still thought the MRL was not the
appropriate reference value to use in the
assessment.
Regarding use of the IRIS RfC for
manganese in the 2011 proposal risk
assessment, commenters stated that the
manganese RfC was outdated, did not
constitute the best available science
(including use of benchmark dose
statistical analyses or physiologicallybased pharmacokinetic models), and
substantial research has been conducted
since the 1993 IRIS RfC was last
updated. The commenters refer to their
own calculations and studies and
developed their own reference value for
manganese and state that the EPA
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should use that value. Regarding use of
the ATSDR MRL for manganese in the
2014 supplemental proposal risk
assessment, the same commenters stated
that the manganese MRL was an
improvement over the IRIS RfC, but was
still not the best available science
because, in their review, ATSDR did not
apply physiologically-based
pharmacokinetic models. The
commenters again refer to their own
calculations and studies developing a
reference value for manganese and state
that EPA should use that value. Another
commenter disagrees with the use of the
ATSDR MRL because the EPA has not
provided sufficient rationale for using a
less-protective value. Instead, this
commenter recommended that we
continue to use the IRIS RfC value.
Response: We agree that there were
newer information and assessments
available at the time of the 2011
proposal and also for the 2014
supplemental proposal, some of which
may use the currently preferred
approach for developing dose-response
values (i.e., the benchmark dose
approach). However, we only use
reference values which meet certain
criteria in regards to how they are
derived (using EPA guidelines or
similar), derived by credible sources
with health-protective goals similar to
those of the EPA, using peer-review
procedures also similar to the level
applied to the EPA values, and with an
open public comment process. We have
a tiered priority list for sources of
chronic dose-response information,
which meet these criteria (as described
in the supplemental proposal, 79 FR
60238). The tiered prioritized list has
been through a SAB review and was
favorably received.
In the risk assessment for the 2011
proposal, we used the IRIS RfC for
chronic exposure to manganese and
received numerous comments regarding
use of that value. In response to those
comments, we considered the existing
peer-reviewed health effect reference
values for chronic inhalation exposure
to manganese from other federal, state,
and international agencies and
organizations. We developed a reference
value array document 2 providing
additional details for the available
values. We noted that the ATSDR MRL
value available for the 2011 proposal
was a draft value. The ATSDR MRL was
subsequently finalized in 2012.
In our consideration of available
reference values, we did not include
2 U.S. EPA. Mn and BTEX Reference Value Arrays
(Final Reports). U.S. Environmental Protection
Agency, Washington, DC, EPA/600/R-12/047F,
2013.
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some values specifically noted in public
comments. The level of peer review for
non-governmental scientific
publications is qualitatively different
than the governmental processes used to
derive the values described in our tiered
prioritized list, and some of the values
in the manganese reference value array
document. The information provided by
these additional references from the
commenter(s) may prove useful in an
IRIS reassessment for manganese, and
we agree that the physiologically-based
models, along with all other relevant
available peer-reviewed literature, will
be considered in any IRIS reassessment
of manganese. Yet, a direct application
of any of these values instead of an
established value in our tiered list of
prioritized dose-response values would
be inconsistent with the EPA policy as
implemented in the RTR Program, and
with recommendations from the SAB.
After considering the values in our
tiered list of prioritized dose-response
values, and consistent with Agency
policy supported by SAB, we decided to
rely on the 2012 ATSDR MRL value for
the 2014 supplemental proposal. Both
the 1993 IRIS RfC and the 2012 ATSDR
MRL were based on the same study
(Roels et al., 1993). In developing their
assessment, ATSDR used updated doseresponse modeling methodology
(benchmark dose approach) and
considered recent pharmacokinetic
findings to support their selection of
uncertainty values in the MRL
derivation.
4. What is the rationale for our final
approach and final decisions for the risk
review?
As noted in section II.A.1 of this
preamble, the EPA sets standards under
CAA section 112(f)(2) using ‘‘a two-step
standard-setting approach, with an
analytical first step to determine an
‘acceptable risk’ that considers all
health information, including risk
estimation uncertainty and includes a
presumptive limit on maximum
individual lifetime risk (MIR) of
approximately 1 in 10 thousand.’’ 3 (54
FR 38045, September 14, 1989).
a. Acceptability Determination. As in
the supplemental proposal, the EPA
concludes that the risks are
unacceptable for the following reasons.
First, the EPA considered the fact that
the noncancer hazard HQ ranges from 4
based on actual emissions to 40 based
on allowable emissions. The EPA has
not established under section 112 of the
CAA a numerical range for risk
3 1-in-10 thousand is equivalent to 100-in-1
million. The EPA currently describes cancer risks
as ‘n-in-1 million.’
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acceptability for noncancer effects as it
has with carcinogens, nor has it
determined that there is a bright line
above which acceptability is denied.
However, the Agency has established
that, as exposure increases above a
reference level (as indicated by a HQ or
TOSHI greater than 1), confidence that
the public will not experience adverse
health effects decreases and the
likelihood that an effect will occur
increases. For the Ferroalloys
Production source category, the
potential for members of the public to
be exposed to manganese at
concentrations up to 40 times the MRL
reduces the Agency’s confidence that
the public is protected from adverse
health effects and diminished the
Agency’s ability to determine that such
exposures are acceptable. Second, the
EPA considered the fact that the cancer
risk estimate for actual emissions is 20in-1 million and up to 100-in-1 million
for allowable emissions. While 20-in-1
million is well within the acceptable
range, risks from allowable emissions
are at the upper end of the range of
acceptability. This fact, combined with
the fact that the noncancer hazard is up
to 40 times the MRL and the refined
multipathway HQ for Hg is at the RfD,
leads the Agency to conclude that the
risk from this source category is
unacceptable.
b. What is EPA requiring in the final
rule to address the unacceptable risks?
As mentioned above, to address the
unacceptable risks, we are promulgating
tighter PM emission limits for the
stacks, which significantly reduces risks
due to allowable emissions.
Furthermore, to reduce risks due to
process fugitive emissions, we are
promulgating a requirement that
facilities must achieve effective
enhanced capture of process fugitive
emissions using a system of primary
hoods (that capture process fugitive
emissions near the source) and/or
secondary capture of fugitives (which
would capture remaining fugitive
emissions near the roof-line). Facilities
must install, operate, and maintain a
process fugitives capture system that is
designed to capture and control 95
percent or more of the process fugitive
emissions. We are also promulgating an
opacity limit of 8 percent to ensure
process fugitive emissions are
effectively captured and controlled.
Facilities will need to meet an average
opacity of 8 percent for the entire
furnace cycle (about 90–120 minutes)
with a maximum opacity of no more
than 20-percent opacity for any 12minute period. Moreover, facilities will
need to monitor various control
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parameters (such as fan speed,
amperage, pressure drops, and/or
damper positioning) to ensure the
process fugitive capture systems and
controls are working properly.
c. Remaining Risks After
Implementation of the Requirements to
Address Unacceptable Risks. To
determine the remaining risks after
implementation of the lower stack PM
emissions limits and requirements to
effectively control process fugitives
(described above), we conducted a post
control risk assessment, which is
described in detail in the document
titled Residual Risk Assessment for the
Ferroalloys Source Category in Support
of the 2015 Final Rule, which is
available in the docket for this
rulemaking.
Based on this post control risk
assessment, we conclude that after the
requirements described above to address
unacceptable risks are implemented, the
risks to public health will be
substantially reduced.
For example, the results of the postcontrol chronic inhalation cancer risk
assessment indicate that the maximum
individual lifetime cancer risk posed by
these two facilities, after the
implementation of the promulgated
controls, will be no higher than 10-in1 million, with an estimated reduction
in cancer incidence to 0.002 cases per
year. In addition, the number of people
estimated to have a cancer risk greater
than or equal to 1-in-1 million would be
26,000. The results of the post-control
risk assessment also indicate that the
maximum chronic noncancer inhalation
TOSHI value would be reduced to 1.
The number of people estimated to have
a TOSHI greater than 1 would be
reduced to 0. We also estimate that after
the implementation of controls, the
maximum worst-case acute HQ value
would be less than 1 (based on REL
values).
Considering post-control emissions of
multipathway HAP, Hg emissions
would be reduced by approximately 3
pounds per year (lbs/yr), lead would be
reduced by about 1,600 lbs/yr,
polycyclic organic matter (POM)
emissions would be reduced by
approximately 3,600 lbs/yr, cadmium
would be reduced by about 150 lbs/yr,
and dioxins and furans would be
reduced by about 0.002 lbs/yr from the
baseline emission rates.
d. Ample Margin of Safety Analysis.
Under the ample margin of safety
analysis, we again considered all of the
health factors evaluated in the
acceptability determination and
evaluated the cost and feasibility of
available control technologies and other
measures (including the controls,
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measures, and costs reviewed under the
technology review) that could be
applied in this source category to
further reduce the risks due to
emissions of HAP identified in our risk
assessment.
As described above, we estimate that
the actions finalized under CAA section
112(f)(2) to address unacceptable risks
will reduce the MIR to 10-in-1 million.
The cancer incidence will be reduced to
0.002 cases per year and the number of
people estimated to have cancer risks
greater than 1-in-1 million will be
reduced to 26,000 people. The chronic
noncancer inhalation TOSHI will be
reduced to 1 and the number of people
exposed to a TOSHI level greater than
1 will be reduced to 0. In addition, the
potential multipathway impacts will be
reduced.
Based on all of the above information,
we conclude that the risks will be
acceptable after implementation of the
lower stack limits for PM and the
control requirements to reduce process
fugitive emissions, as we concluded in
the supplemental proposal. Based on
our research and analysis, we did not
identify any cost-effective controls
beyond those described above that
would achieve further reduction in risk.
While in theory, the 2011 proposed
approach of total enclosure with
negative pressure would provide some
additional risk reduction, the additional
risk reduction is minimal and, similar to
our assessment and conclusions
described in the supplemental proposal,
we continue to believe the total
enclosure approach would not be
economically feasible and may not be
technically feasible for these facilities.
No other technology advances were
identified during the comment period.
Therefore, we are not promulgating any
additional requirements under the
ample margin of safety analysis beyond
the requirements being finalized to
address unacceptable risks (as described
above). We conclude that the controls to
achieve acceptable risks will also
provide an ample margin of safety to
protect public health.
B. Technology Review for the
Ferroalloys Production Source Category
1. What did we propose pursuant to
CAA section 112(d)(6) for the
Ferroalloys Production source category?
Pursuant to CAA section 112(d)(6), we
conducted a technology review, which
focused on identifying and evaluating
developments in practices, processes,
and control technologies for the
emission sources in the Ferroalloys
Production source category. For the
2011 proposal (76 FR 72508), we
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identified developments in practices,
processes or control technologies for PM
emissions from stacks (as a surrogate for
metal HAP) and for process fugitive
metal HAP emissions. Based on the
comments received from the public and
information received through a 2012
ICR, we revised both the technology
review and risk assessment for the
Ferroalloys Production source category,
which were described in detail in the
2014 supplemental proposal (79 FR
60238).
a. PM Emission Limits From Stacks.
For PM stack emissions limits, we
determined for the 2011 proposal that
the test data received from the two
facilities indicate that all five furnaces
that are in operation have PM emission
levels that are well below their
respective emission limits in the 1999
MACT rule, which were based on size
and product being produced. The test
data received from the facilities also
indicate that the PM emission levels for
MOR and crushing and sizing are well
below their respective emission limits
in the 1999 MACT rule. These findings
demonstrate that add-on particulate
control technologies (Venturi scrubber,
positive pressure fabric filter, negative
pressure fabric filter) used to control
emissions from the sources are effective
in reducing PM (used as a surrogate for
metal HAP). Based on these findings, in
2011 we proposed a PM limit of 24 mg/
dscm corrected to 2 percent carbon
dioxide (CO2) for existing furnaces.
We received additional test data after
the 2011 proposal and re-evaluated the
PM limit using available PM emissions
test data and consideration of variability
across these data. Based on this
analysis, we determined that it was
appropriate to propose a revised PM
limit of 25 mg/dscm for existing
furnaces. No additional add-on control
is expected to be required by the
facilities to meet this revised existing
source limit. To demonstrate
compliance, we proposed these sources
would be required to conduct periodic
performance testing and develop and
operate according to a baghouse
operating plan or continuously monitor
Venturi scrubber operating parameters.
We also proposed that furnace
baghouses would be required to be
equipped with bag leak detection
systems (BLDS).
For the 2011 proposal, the proposed
new source PM standard was
determined by evaluating the available
data from the best performing furnace
(which was determined to be furnace #2
at Felman). The proposed new source
limit was determined to be 9.3 mg/
dscm. We received additional test data
after the 2011 proposal and re-evaluated
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the new source limit using the available
test data. The revised new source PM
standard for furnaces for the 2014
supplemental proposal was determined
by evaluating the available data from the
best performing furnace (which was
again determined to be furnace #2 at
Felman). The new source MACT limit
was determined to be 4.0 mg/dscm
based on data from furnace #2 and was
proposed as the MACT emissions limit
for PM from new and reconstructed
source furnace stacks in the 2014
supplemental proposal.
The PM emission limit for the local
ventilation control device outlet was
also re-evaluated using compliance test
data and test data from the 2012 ICR. A
local ventilation control system is used
to capture tapping, casting, or ladle
treatment emissions and direct them to
a control device other than one
associated with the furnace. The 2011
proposal included a proposed PM limit
for the local ventilation control device
that was based on PM data from the
furnaces. After the 2011 proposal, we
received test data from three different
emissions tests (for a total of nine test
runs) specifically for this local
ventilation source. We determined these
data were more appropriate for the
development of a limit for this source
than the furnace data we had used for
the 2011 proposal. There is currently
only one local ventilation control device
outlet emissions source in this source
category. Using the new data for the one
existing local ventilation source, we
calculated a revised emissions limit of
4.0 mg/dscm and determined that this
was an appropriate emissions limit for
this source. Therefore, we proposed an
emissions limit of 4.0 mg/dscm for
existing, new, and reconstructed local
ventilation control device emissions
sources in the supplemental proposal.
For crushing and screening
operations, we proposed an emission
limit of 13 mg/dscm for new and
existing crushing and sizing operations
in the 2011 proposal. We did not receive
any additional data for this emission
source and, therefore, made no revisions
to this proposed limit in the 2014
supplemental proposal.
The MOR operation is a unique
process that is operated by only one
facility (Eramet). We calculated a
proposed emission limit of 3.9 mg/dscm
in the 2011 proposal that would apply
to both new and existing MOR operation
sources. We did not receive any
additional data for this emission source
and, therefore, made no revisions to this
proposed limit in the 2014
supplemental proposal.
b. Emission Standards for Process
Fugitives. For process fugitive metal
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HAP emissions, we identified two
potential developments in practices and
control techniques. One option would
require facilities to install and operate
enhanced capture of process fugitive
emissions using a combination of
primary hoods and ductwork in close
proximity to the emission sources, such
as tapping or casting and/or secondary
hoods located near the roofline. Another
option would be to require full
enclosure of the furnace building(s)
with negative pressure and evacuate the
process fugitive emissions to a control
device(s). In the 2011 proposal, we
proposed that the full furnace building
enclosure option represented an
advance in emission control measures
since the Ferroalloys Production
NESHAP was originally promulgated in
1999.
For day-to-day continuous monitoring
to demonstrate compliance with the
proposed full building enclosure
requirements, the 2011 proposal relied
mainly on requiring monitoring
differential pressure to ensure facilities
maintained a negative pressure of at
least 0.007 inches of water and that
emissions within the facilities would
need to be vented to PM control devices.
This was to be supplemented by
operation and work practice standards
that required preparation of a process
fugitive emissions ventilation plan for
each shop building. In the 2011
proposal, we also proposed a
requirement that emissions exiting from
a shop building may not exceed more
than 10-percent opacity for more than
one 6-minute period, to be
demonstrated every 5 years as part of
the periodic required performance tests.
We received significant comments in
response to the 2011 proposal.
Commenters claimed that we had
significantly underestimated the costs
for full building enclosure and that it
would not be feasible for these facilities.
After reviewing and considering the
comments along with other information,
we decided to re-evaluate the proposed
requirement for negative pressure
ventilation and consider other options.
Based on our re-evaluation, for the
2014 supplemental proposal, we
concluded that the full-building
enclosure option may not be feasible
and would have significant economic
impacts on the facilities. However, we
concluded that an option based on
enhanced local capture and control of
process fugitive emissions using a
combination of primary and secondary
hoods is a feasible and cost-effective
approach to achieve significant
reductions in process fugitive HAP
emissions. Therefore, in the 2014
supplemental proposal, we proposed
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that facilities would need to install and
operate a local capture system using a
combination of primary and/or
secondary hoods that is designed to
achieve at least 95-percent capture and
control of process fugitive emissions.
With the move to the proposed
enhanced local capture alternative in
the 2014 supplemental proposal, we no
longer had a day-to-day continuous
requirement of monitoring negative
pressure. Instead, in the 2014
supplemental proposal, continuous
compliance demonstration would be
based mainly on meeting an opacity
limit, monitoring ventilation parameters
(such as fan speed, amperage, and/or
damper positioning), and documenting
the design of the system to achieve 95percent capture. Since opacity
monitoring would be a primary method
to demonstrate continuous compliance,
we proposed that facilities would need
to meet an average opacity of 8 percent
for an entire furnace cycle (about 90–
120 minutes) with a maximum opacity
of no more than 20 percent opacity for
any 12-minute period. Furthermore, we
proposed facilities would need to
monitor opacity for a full furnace cycle
(about 90–120 minutes) at least once per
week per furnace building. We also
proposed that, if the average opacity
reading from the shop building is
greater than 8-percent opacity during an
observed furnace process cycle, an
additional two more furnace process
cycles must be observed such that the
average opacity during the entire
observation period is less than 7-percent
opacity. A furnace process cycle means
the period in which the furnace is
tapped to the time in which the furnace
is tapped again and includes periods of
charging, smelting, tapping, casting, and
ladle raking.
Regarding the design requirements, in
the supplemental proposal, we
proposed that the facilities in this
source category must install, operate,
and maintain a process fugitives capture
system that is designed to collect 95
percent or more of the process fugitive
emissions from furnace operations,
casting MOR process, ladle raking, and
slag skimming and crushing and
screening operations and convey the
collected emissions to a control device
that meets specified emission limits and
the proposed opacity limits. We
proposed that this plan be submitted to
the permitting authority, incorporated
into the source’s operating permit and
updated every 5 years or when there is
a significant change in variables that
affect process fugitive emissions
ventilation design. We proposed that
this list of design criteria, coupled with
the requirement for frequent opacity
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observations and operating parameter
monitoring, would ensure process
fugitive emissions are effectively
controlled and would result in
enforceable requirements.
More information concerning our
proposed technology review can be
found in the memoranda titled, Revised
Technology Review for the Ferroalloys
Production Source Category, and Cost
Impacts of Control Options Considered
for the Ferroalloys Production NESHAP
to Address Fugitive HAP Emissions,
which are available in the docket, and
in the preamble to the 2014
supplemental proposed rule, 79 FR at
60271 to 60273.
2. How did the technology review
change for the Ferroalloys Production
source category?
For the October 6, 2014, supplemental
proposal, we solicited comment
regarding the use of new technologies to
provide continuous or near continuous
long term approaches to monitoring
emissions from industrial sources for
the Ferroalloy Production source
category. After considering comments
received and after evaluating the
technologies further, we are replacing
the weekly Method 9 opacity
requirement with a weekly requirement
to measure opacity using ASTM D7520–
13 and DCOT to demonstrate
compliance with the process fugitives
standards. The final rule amendments
require facilities to use the DCOT to
measure opacity at least once per week
for each of the furnace and MOR
buildings to demonstrate compliance
with the opacity limits. However, as
mentioned above, facilities will have the
opportunity to reduce the frequency of
opacity readings to monthly after 26
consecutive weeks of compliant weekly
readings. The facilities would still be
required to meet an average opacity
standard of 8-percent opacity for the
furnace cycle (90–120 minutes) and at
no time during operation may any two
consecutive 6-minute block opacity
readings be greater than 20-percent
opacity. The cost of implementing the
DCOT system is estimated to be
approximately $200,000 per year for the
source category with weekly readings.
However, these costs decrease to about
$90,000 per year for the source category
if they do monthly readings per furnace
building. All other requirements we
proposed under CAA section 112(d)(6)
in the supplemental proposal have not
changed.
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3. What key comments did we receive
on the technology review, and what are
our responses?
Several comments were received
regarding the technology review for the
Ferroalloys Production source category.
The following is a summary of the more
significant comments and our responses
to those comments. Other comments
received and our responses to those
comments can be found in the
document titled National Emission
Standards for Hazardous Air Pollutant
Emissions: Ferroalloys Production
Summary of Public Comments and the
EPA’s Responses on Proposed Rule (76
FR 72508, November 23, 2011) and
Supplemental Proposal (79 FR 60238,
October 6, 2014), which is available in
the docket for this action (EPA–HQ–
OAR–2010–0895).
Comment: One commenter supported
the EPA’s decision to re-evaluate the
feasibility and cost-effectiveness of the
controls that the Agency proposed in its
2011 proposal. However, the commenter
objects to the EPA’s conclusion that an
alternative system involving both
primary and secondary capture is
available and represents an
‘‘advancement in technology’’ pursuant
to CAA section 112(d)(6). The
commenter states that this type of
system does not currently exist in
practice at any ferroalloy operation.
They explain that, in theory, such a
system appears likely to provide some
degree of additional reductions.
However, the commenter notes some of
the specific potential control methods
mentioned by the EPA have already
been proven not to work. As an
example, the commenter states that
curtains have previously been installed
in an attempt to contain additional
furnace emissions, but the curtains
burned up due to the extreme heat in
only a few weeks. The commenter,
therefore, objects both to the
characterization of these additional
controls as a currently available
‘‘advancement in technology,’’ and to
the EPA’s conclusion that the cost of
almost $100,000 per ton of HAP
reductions for these additional controls
is cost effective.
Response: In their supplemental
comments on the 2011 proposed rule,
industry representatives provided
suggested alternative designs to address
fugitive emissions from the furnace
buildings. The designs suggested by the
industry representatives included
improving the existing primary hooding
and capture systems close to the
emissions sources and/or adding
secondary capture to ensure effective
capture and control of process fugitive
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emissions. The use of a primary hooding
and exhaust system in conjunction with
general secondary hooding and exhaust
system was estimated to provide a total
capture of 95 percent of process fugitive
emissions, including emissions from the
tapping, casting, crushing/screening,
and skimming/slag raking processes.
We reviewed these designs and
discussed the designs with ventilation
experts. The ventilation experts agreed
that the suggested primary system along
with secondary capture could achieve
95 percent reduction of process fugitive
emissions from the buildings. They
noted that many of the designs and
improvements were based on the
elements of good ventilation systems
that are used in other industries to
capture and control fugitive emissions.
Because these designs have been only
partially deployed in this industry, they
constitute a relevant development in
technology beyond what is required by
the current rule. We view the successful
deployment of these technologies in
other industries and the expert
judgement of industrial ventilation
experts as establishing that the
technologies are technically available
for transfer to the Ferroalloy Production
source category.
As part of our technology review, we
evaluated the costs and effectiveness of
a regulatory option that is based on the
general emission control scenario
suggested by the industry
representatives which would include a
system of primary and/or secondary
hooding designed to capture 95 percent
of process fugitive emissions. The
process fugitive emissions would be
captured by the primary and/or
secondary hoods and routed to PM
control devices. This option for the
control of process fugitive emissions
under CAA section 112(d)(6) is exactly
the same option that we are
promulgating under CAA section
112(f)(2) to capture and control fugitives
(described in section IV.A of this
preamble). We estimate that the total
capital cost including monitoring would
be about $40.3 million, the total
annualized costs would be about $7.7
million per year, and that it would
achieve 77 tpy reduction of HAP, mostly
manganese and other HAP metals (e.g.,
cadmium compounds, chromium
compounds, nickel compounds) and
also achieve about 229 tpy reduction of
PM. Based on our evaluation, we
conclude that installing and operating
such a system is a feasible and costeffective approach to achieve significant
reductions in process fugitive HAP
emissions and will achieve almost as
much reductions as the full building
enclosure option (229 vs. 252 tons PM
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reductions). In light of the technical
feasibility and cost effectiveness of this
enhanced fugitive capture option (that
includes a combination of primary
capture and/or secondary capture
designed to capture and control 95
percent of process fugitive), we are
promulgating this option under the
authority of section 112(d)(6) of the
CAA. The control requirements and
compliance requirements under this
CAA section 112(d)(6) option are the
exact same requirements we are
promulgating under CAA section
112(f)(2) to address unacceptable risks
for process fugitive emissions (described
in section IV.A of this preamble). As
described in that section, facilities must
install, operate, and maintain a process
fugitives capture system that is designed
to capture 95 percent or more of the
process fugitive emissions. Facilities
will also need to meet an average
opacity of 8 percent for each furnace
cycle (about 90–120 minutes) with a
maximum opacity of no more than 20
percent opacity for any two consecutive
6-minute block opacity readings (12minute period). To demonstrate
compliance, facilities will need to
initially monitor opacity for a full
furnace cycle (about 90–120 minutes) at
least once per week per furnace building
using the DCOT. Moreover, facilities
will need to monitor various control
parameters (such as fan speed,
amperage, pressure drops, and/or
damper positioning) to ensure the
fugitive capture system and controls are
working properly.
Comment: One commenter states that
the only notable development that
occurred in ferroalloys emission
practices, processes, and control
technologies since the 1999 NESHAP
took effect is the installation of
scrubbers and baghouses. Since
scrubbers and baghouses have
demonstrably different performance in
controlling particulate emissions, the
commenter claims that developments
since 1999 warrant separate particulate
emission limits based on the type of
control device involved. The commenter
states that the EPA did not acknowledge
this development and proposed a single
stack particulate limit for all furnaces.
The commenter provided proposed PM
limits of 27 mg/dscm for wet particulate
scrubbers and 6.2 mg/dscm for
baghouses, and notes that these limits
would actually reduce the total
allowable particulate emissions from
their facility in comparison to the EPA’s
proposed single limit of 25 mg/dscm.
Response: Section 112 of the CAA
grants the EPA discretion to establish
‘‘categories and subcategories’’ of
sources to be regulated under CAA
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section 112, and further allows the EPA
to ‘‘distinguish among classes, types and
sizes of sources within a category or
subcategory’’ when establishing MACT
standards. However, we believe it is not
appropriate to establish subcategories
based on type of control technology
used by these emission sources.
In the case of the PM emissions from
the ferroalloy furnaces, we believe if it
was appropriate, we could subcategorize
based on the size of the furnace or the
product being produced in that furnace.
However, we determined that there was
no statistical difference in PM emissions
based on the size of the individual
furnaces or by the product being
produced in those furnaces. Therefore,
we decided it was not appropriate to
subcategorize for PM emissions and
instead established a single PM limit for
all of the furnaces, regardless of size or
product being produced.
Comment: One commenter believes
that the EPA’s proposed requirements to
reduce process fugitive emissions under
CAA section 112(d)(6) are not based on
control practices in use in the
ferroalloys industry, but rather simply
reflect a decision by the EPA that the
sources at Eramet and Felman should be
subject to additional requirements. By
putting the enhanced fugitive control
requirements under CAA section
112(d)(6), the commenter believes that
the EPA dispenses with any attempt to
justify the requirements as cost
effective, as would be required to
impose for ‘‘beyond the MACT floor’’
standards under CAA section 112(d)(2),
and the EPA dispenses with any attempt
to present a risk-based justification for
the requirements, as would be required
under CAA section 112(f)(2).
Response: As an initial matter, we
note the process fugitive control
requirements are justified as risk-based
requirements under CAA section
112(f)(2). See section IV.A of this
preamble. Therefore, the premise of this
comment is factually incorrect. That
said, the requirements of this rule also
are justified under CAA section
112(d)(6). Under CAA section 112(d)(6),
we are required to review emission
standards no less frequently than every
8 years and revise them ‘‘as necessary
(taking into account developments in
practices, processes, and control
technologies).’’ The ferroalloys industry
already includes some of the controls
envisioned under this control scenario.
For example, all 5 furnaces in the source
category in the U.S. already have some
type of primary hooding to capture
some process fugitive emissions from
tapping and/or casting operations. In
fact, one of the five furnaces in the U.S.
already achieves good capture of
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tapping emissions with their current
configuration. Furthermore, effective
primary and secondary capture systems
are currently used in other metals
industries (e.g., steel production,
secondary lead production) to
effectively capture and control process
fugitives.
Moreover, as described above,
representatives from the ferroalloys
companies have provided suggestions as
to how such a system could be
designed, installed and operated to
achieve 95-percent capture of fugitives.
Therefore, we conclude such a system is
technically feasible. Furthermore, as we
described above, we conclude these
controls would be cost effective
($91,000 per ton of HAP metal reduced).
Therefore, we conclude it is appropriate
to promulgate this control option under
section 112(d)(6) of the CAA.
4. What is the rationale for our final
approach for the technology review?
a. PM Emissions Limits from Stacks.
The available test data from the five
furnaces located at the two facilities
indicate that all of these furnaces have
PM emission levels that are well below
their respective emission limits in the
1999 MACT rule. These findings
demonstrate that the add-on emission
control technologies (Venturi scrubber,
positive pressure fabric filter, negative
pressure fabric filter) used to control
emissions from the furnaces are
effective in reducing particulate matter
(used as a surrogate for metal HAP).
The PM emissions, used as a surrogate
for metal HAP, that were reported by the
industry in response to the 2010 ICR,
were far below the level specified in the
current NESHAP, indicating
improvements in the control of PM
emissions since promulgation of the
current NESHAP. We re-evaluated the
data received in 2010, along with
additional data received in 2012 and
2013, to determine whether it is
appropriate to promulgate revised
emissions limits for PM from the
furnace process vents. More details
regarding the available PM data and this
re-evaluation are provided in the
Revised Technology Review for the
Ferroalloys Production Source Category
for the Supplemental Proposal, which is
available in the docket. Unlike PAH and
Hg stack data, we did not see significant
differences in emissions based on
product produced (e.g., FeMn or SiMn).
Therefore, we are not promulgating
separate PM stack limits based on
product type.
Based on this analysis, we determined
it is appropriate to finalize the revised
existing source furnace stack PM
emissions limit of 25 mg/dscm, which is
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the same limit we proposed in the
supplemental proposal. No additional
add-on controls are expected to be
required by the facilities to meet the
revised existing source limit of 25 mg/
dscm. However, this revised limit will
result in significantly lower ‘‘allowable’’
PM emissions from the source category
compared to the level of emissions
allowed by the 1999 MACT rule and
would help prevent any emissions
increases. To demonstrate compliance,
these sources will be required to
conduct periodic performance testing
and develop and operate according to a
baghouse operating plan or
continuously monitor Venturi scrubber
operating parameters. Also furnace
baghouses will be required to be
equipped with BLDS.
The final PM standard for new and
reconstructed furnaces is 4.0 mg/dscm
and was determined by evaluating the
available data from the best performing
furnace (which was determined to be
furnace #2 at Felman).
As described above, the PM emission
limit for the local ventilation control
device outlet was re-evaluated for the
supplemental proposal using
compliance test data and test data from
the 2012 ICR. We did not receive any
additional data since the supplemental
proposal for this source. Using all the
available data for the one existing local
ventilation source, we calculated an
emissions limit of 4.0 mg/dscm, which
is the exact same limit we proposed in
the supplemental proposal. We
conclude that this is still an appropriate
emissions limit for this source.
Therefore, we are promulgating this
emissions limit of 4.0 mg/dscm for
existing, new, and reconstructed local
ventilation control device emissions
sources. In addition, we are
promulgating a PM limit of 3.9 mg/dscm
for any new, reconstructed, or existing
MOR process, and a PM limit of 13 mg/
dscm for any new, reconstructed, or
existing crushing and screening
equipment, which are consistent with
what we proposed in our November 23,
2011, proposal.
Furthermore, as mentioned in section
III of this preamble, we are
promulgating a PM limit of 3.9 mg/dscm
for any new, reconstructed, or existing
MOR process, and a PM limit of 13 mg/
dscm for any new, reconstructed, or
existing crushing and screening
equipment.
2. Standards for Process Fugitive Metal
HAP Emissions
In the 2011 proposal, we proposed a
requirement for sources to enclose the
furnace building, collect fugitive
emissions such that the furnace building
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is maintained under negative pressure,
and duct those emissions to control
devices. As described above,
commenters on the 2011 proposal
disagreed with our assessment.
Commenters also raised concerns
about worker safety and comfort in
designing and operating full enclosure
systems. We believe that such issues can
be overcome with proper ventilation
design and installation of air
conditioning systems and other steps to
ensure these issues are not a problem.
However, after further review and
evaluation, we conclude that it would
be quite costly for these facilities to
become fully enclosed with negative
pressure and achieve the appropriate
ventilation and conditioning of indoor
air.
We re-evaluated the costs and
operational feasibility associated with
the full building enclosure with
negative pressure. We consulted with
ventilation experts who have worked
with hot process fugitives similar to
those found in the ferroalloys industry
(e.g., electric arc furnace steel minimills and secondary lead smelters). We
determined that substantially more air
flow, air exchanges, ductwork, fans and
control devices and supporting
structural improvements would be
needed (compared to what we had
estimated in the 2011 proposal) to
achieve negative pressure and also
ensure adequate ventilation and air
quality in these large furnace buildings.
Therefore, as explained in the
supplemental proposal, we determined
that the proposed negative pressure
approach presented in the 2011
proposal would be much more
expensive than what we had estimated
in 2011 and may not be feasible for
these facilities.
As mentioned above, for the
supplemental proposal, we also
evaluated another option based on
enhanced capture of the process fugitive
emissions using a combination of
effective local capture with primary
hooding close to the emissions sources
and/or secondary capture of remaining
fugitives with roof-line capture hoods
and control devices. These buildings are
currently designed such that fugitive
emissions that are not captured by the
primary hoods flow upward with a
natural draft to the open roof vents and
are vented to the atmosphere
uncontrolled. Under our enhanced
control scenario, the primary capture
close to the emissions sources would be
significantly improved with effective
local hooding and ventilation and the
remaining fugitive emissions (that are
not captured by the primary hoods)
would be drawn up to the roof-line and
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captured with secondary hooding and
vented to control devices.
In cases where additional collection
of fugitives from the roof areas is needed
to comply with the rule, fume collection
areas may be isolated via baffles (so the
area above the furnace where fumes
collect may be kept separated from
‘‘empty’’ spaces in large buildings) and
roof openings over fume collection areas
can be sealed and fumes directed to
control devices. The fugitive emission
capture system should achieve inflow at
the building floor, but outflow toward
the roof where most of the remaining
fugitives would be captured by the
secondary hooding. We concluded that
a rigorous, systematic examination of
the ventilation requirements throughout
the building is the key to developing a
fugitive emission capture system
(consisting of primary hoods, secondary
hoods, enclosures, and/or building
ventilation ducted to PM control
devices) that can be designed and
operated to achieve very low levels of
fugitive emissions. Such an evaluation
considers worker health, safety, and
comfort and it is designed to optimize
existing ventilation options (fan
capacity and hood design). Thus, we
concluded that an enhanced capture
system based on these design principles
does represent an advancement in
technology. We estimate that this type
of control system could capture 95
percent of the process fugitive emissions
and vent those emissions to PM control
devices. This enhanced local capture
option is described in more detail in the
Revised Technology Review for the
Ferroalloys Production Source Category
and in the Cost Impacts of Control
Options to Address Fugitive HAP
Emissions for the Ferroalloys Production
NESHAP Supplemental Proposal
documents, which are available in the
docket.
Under this control option, the cost
elements vary by plant and furnace and
include the following:
• Curtains or doors surrounding
furnace tops to contain fugitive
emissions;
• Improvements to hoods collecting
tapping emissions;
• Upgrade fans to improve the airflow
of fabric filters controlling fugitive
emissions;
• Addition of ‘‘secondary capture’’ or
additional hoods to capture emissions
from tapping platforms or crucibles;
• Addition of fugitives capture for
casting operations;
• Improvement of existing control
devices or addition of fabric filters; and
• Addition of rooftop ventilation, in
which fugitive emissions escaping local
capture are collected in the roof canopy
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over process areas through addition of
partitions, hoods, and then directed
through ducts to control devices.
We estimate the total capital costs of
installing the required ductwork, fans
and control devices under the enhanced
capture option (which is described
above and in more detail in the Cost
Impacts of Control Options to Address
Fugitive HAP Emissions for the
Ferroalloys Production NESHAP
Supplemental Proposal document) to be
$40.3 million and the total annualized
cost to be $7.7 million for the two
plants. The total estimated HAP
reduction for the enhanced capture
option is 77 tpy at a cost per ton of
$103,000 ($52 per pound). We also
estimate that this option would achieve
PM emission reductions of 229 tpy,
resulting in cost per ton of PM removed
of $34,600 per ton and achieve
particulate matter 2.5 microns and less
(PM2.5) emission reductions of 48 tons
per year, resulting in a cost per ton of
PM2.5 removal of $165,000 per ton. We
believe these controls for process
fugitive HAP emissions (described
above), which are based on enhanced
capture (with primary and secondary
hooding) are feasible for the Ferroalloys
Production source category from a
technical standpoint and are cost
effective. These cost effectivenesses are
in the range of cost effectiveness for PM
and HAP metals from other previous
rules. However, it is important to note
that there is no bright line for
determining acceptable cost
effectiveness for HAP metals. Each
rulemaking is different and various
factors must be considered. Some of the
other factors we consider when making
decisions whether to establish standards
beyond-the-floor (BTF) under CAA
section 112(d)(2) or under CAA section
112(d)(6) include, but are not limited to,
the following: which of the HAP metals
are being reduced and by how much;
total capital costs; annual costs; and
costs compared to total revenues (e.g.,
costs to revenue ratios).
As described in the supplemental
proposal, we also re-evaluated the
option based on full building enclosure
with negative pressure.
Based on those analyses, we
concluded in the supplemental proposal
and conclude again in this action that
the full-building enclosure option with
negative pressure may not be feasible
and would have significant economic
impacts on the facilities (including
potential closure for one or more
facilities). Therefore, we are not
promulgating an option based on full
building enclosure with negative
pressure.
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However, consistent with the
supplemental proposal, we conclude
that the enhanced local capture option
is a feasible and cost-effective approach
to achieve significant reductions in
fugitive HAP emissions and will achieve
almost as much reductions as the fullbuilding enclosure option (229 vs. 252
tons PM reductions) and, thus,
achieving most of the emission
reductions at significantly lower costs.
In light of the technical feasibility and
cost effectiveness of the enhanced
capture option, we are promulgating the
enhanced capture option under the
authority of section 112(d)(6) of the
CAA.
Regarding monitoring requirements,
as described above, in the 2011
proposal, we proposed that facilities
would need to conduct day-to-day
continuous monitoring of differential
pressure to comply with the proposed
full building enclosure with negative
pressure requirements.
With the move to the enhanced local
capture alternative option, there is no
longer any requirement to monitor
negative pressure. Under this option,
the main ongoing compliance
requirements will be based on opacity
readings and parametric monitoring.
Therefore, since opacity is a main
method of monitoring compliance for
process fugitive emissions controls, we
believe that frequent opacity monitoring
is necessary, as reflected in the
supplemental proposal. Furthermore, as
we explained in the supplemental
proposal, we believe an average opacity
limit of 8 percent is appropriate to
ensure effective capture and control of
process fugitive emissions over the
entire furnace cycles and that a
maximum opacity of 20 percent for any
2 consecutive 6-minute periods is
appropriate to prevent spikes in fugitive
emissions. Therefore, we are
promulgating an average opacity limit of
8 percent and a maximum opacity limit
of 20 percent for any 2 consecutive 6minute periods.
Regarding opacity monitoring, we are
promulgating a requirement that
facilities conduct opacity observations
at least once per week for a full furnace
cycle for each operating furnace and
each MOR operation using the DCOT
instead of Method 9. We believe the
DCOT is appropriate for the final rule
because it provides more objective and
better substantiated opacity readings.
However, as described above, we are
allowing an opportunity for facilities to
decrease frequency of opacity
monitoring to monthly after 26
compliant weekly readings.
Similar to the supplemental proposal,
we are also finalizing the requirement
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that, if the average opacity reading from
the shop building is greater than 8percent opacity during an observed
furnace process cycle, an additional two
more furnace process cycles must be
observed such that the average opacity
during the entire observation period is
less than 7-percent opacity. A furnace
process cycle means the period in
which the furnace is tapped to the time
in which the furnace is tapped again
and includes periods of charging,
smelting, tapping, casting, and ladle
raking.
As mentioned above, we are also
promulgating the requirement that at no
time during operation may any two
consecutive 6-minute block opacity
readings be greater than 20-percent
opacity.
We believe that the source should
demonstrate that the overall design of
the ventilation system is adequate to
achieve the final standards. Therefore,
we are promulgating the requirement
that facilities in this source category
must install, operate, and maintain a
process fugitives capture system that is
designed to collect 95 percent or more
of the process fugitive emissions from
furnace operations, casting MOR
process, ladle raking and slag skimming
and crushing, and screening operations,
and convey the collected emissions to a
control device that meets specified
emission limits and the opacity limits.
We are also requiring continuous
monitoring of key ventilation operating
system parameters and periodic
inspections of the ventilation systems to
ensure that the ventilation systems are
operating as designed.
We believe that if the facilities design
the capture and control systems
according to the most recent (at the time
of construction) ventilation design
principles recommended by the
American Conference of Governmental
Industrial Hygienists (ACGIH),
including detailed schematics of the
ventilation system design, addressing
variables that affect capture efficiency
such as cross drafts and describes
protocol or design characteristics to
minimize such events and identifies
monitoring and maintenance steps, the
plan will be capable of ensuring the
system is properly designed and
continues to operate as designed.
Therefore, we are promulgating the
requirement that facilities develop such
a plan and submit this plan to the
permitting authority. The plan must also
be incorporated into the source’s
operating permit and updated every 5
years or when there is a significant
change in variables that affect process
fugitive emissions ventilation design.
This design plan, coupled with the
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requirement for frequent opacity
observations and operating parameter
monitoring, will ensure fugitive
emissions are effectively controlled and
will result in enforceable requirements.
We recognize that other design
requirements and/or more frequent
opacity observations may yield more
compliance certainty, but incur greater
costs and not result in measurable
decreases in emissions.
We believe the additional PM data we
received justifies the revised PM stack
emission limits we are promulgating
under the authority of section 112(d)(6)
of the CAA. We also believe the
enhanced capture and control is a
development in technology that is
feasible and cost effective, so we are
promulgating the enhanced local
capture and control option under the
authority of section 112(d)(6) of the
CAA. Furthermore, we believe it is
appropriate to promulgate the DCOT to
ensure adequate furnace capture and
control.
C. CAA Section 112(d)(2) & (3)
Revisions for the Ferroalloys Production
Source Category
1. What did we propose pursuant to
CAA section 112(d)(2) & (3) for the
Ferroalloys Production source category?
In the November 23, 2011, proposal,
we proposed a formaldehyde emission
limit of 201 mg/dscm for any new,
reconstructed, or existing electric arc
furnace.
In the October 6, 2014, supplemental
proposal, we proposed the following:
• HCL emission limit of 180 mg/dscm
for new or reconstructed electric arc
furnaces and 1,100 mg/dscm for existing
electric arc furnaces;
• Hg emission limit of 17 mg/dscm for
new or reconstructed electric arc
furnaces producing FeMn, and 170 mg/
dscm for existing electric arc furnaces
producing FeMn;
• Hg emission limit of 4 mg/dscm for
new or reconstructed electric arc
furnaces producing SiMn and 12 mg/
dscm for existing electric arc furnaces
producing SiMn;
• PAH emission limit of 880 mu;g/
dscm for new or reconstructed electric
arc furnaces producing FeMn and 1,400
mg/dscm for existing electric arc
furnaces producing FeMn; and
• PAH emission limit of 72 mg/dscm
for new or reconstructed electric arc
furnaces producing SiMn and 120 mg/
dscm for existing electric arc furnaces
producing SiMn.
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2. How did the CAA section 112(d)(2) &
(3) revisions change for the Ferroalloys
Production source category?
In mid-August 2014, a few weeks
prior to the signature of the
supplemental proposal, we received a
test report with Hg and PAH data,
which we were unable to incorporate
into the proposed limits in the
supplemental proposal, in part because
of the timing and in part because we
had not completed our review and
technical analysis of the data. We noted
receipt of the data and invited comment
on it in the supplemental proposal, and
made the data available for review. We
committed to considering these data in
the final rule based on public comment
and our technical analysis. In addition
to the pre-supplemental proposal data,
another Hg and PAH test report was
received during the comment period.
The new test data for FeMn production
received in August 2014 and during the
comment period had much higher PAH
concentrations than the data that were
previously provided. The new PAH test
data for SiMn production were only
slightly higher than previous data
received from the facilities. The new Hg
data for both FeMn and SiMn
production were comparable to the test
data that we used to develop the
proposed limits for the supplemental
proposal.
For this action, we re-evaluated the
PAH and Hg emission limits to include
the new test data. The 99-percent upper
prediction limit (UPL) calculation using
all the available reliable data for PAH
emissions results in an emissions limit
of 12,000 mg/dscm for existing furnaces
producing FeMn and 130 mg/dscm for
existing furnaces producing SiMn.
With regard to new source limits, as
mentioned previously, there are only
two furnaces in the source category that
produce FeMn, and both furnaces are
located at Eramet. The units are similar
in design and process the same types of
raw materials, and we, therefore, expect
little or no difference in the
performance of these units. The
available emissions data, which show
that the two units mean emissions are
only 2-percent different, support this
hypothesis. We conclude, based on the
similarities in the units and the
available data, that these two furnaces
achieve the same degree of control of
PAH emissions with their current
control devices. Accordingly, we
consider these two units to be equal
performers with regard to PAH
emissions and therefore, we used all the
data from both units to calculate the
new source emissions limit. Using the
99-percent UPL calculation, we derive
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an emissions limit of 11,500 mg/dscm for
new furnaces producing FeMn.
For SiMn, there were no changes to
the best performing source and the PAH
limit of 72 mg/dscm proposed in the
supplemental proposal is the same limit
selected for the final rule for new
furnaces producing SiMn.
The 99-percent UPL for PAHs for
FeMn production is about 8 times
higher than the proposed PAH limit for
FeMn in the supplemental proposal,
whereas the 99-percent UPL for PAHs
for SiMn production is comparable to
the proposed limit in the supplemental
proposal. The new data show there is
substantial variability in PAH emissions
from the furnaces, especially during
FeMn production.
As mentioned in section III.E of this
preamble, due to the large variation in
PAH emissions from furnace stacks
during FeMn production, we are
requiring quarterly compliance tests for
PAHs (i.e., four PAH compliance tests
per year) for furnaces while producing
FeMn, with an opportunity for facilities
to apply for decreased frequency of such
compliance testing from their permit
authority after the first year and after
four or more successful PAH
compliance tests have been completed
and submitted to the permit authority.
We expect that any application
submitted by an affected source to
request reduced frequent compliance
testing for PAHs should include
information regarding the four or more
compliant test results and what factors
or conditions are contributing to the
quantity and variation of PAH
emissions. For example, the application
could include, among other things,
information about the amounts and
types of input materials, types of
electrodes used, electrode consumption
rates, furnace temperature and other
furnace, process or product information
that may be affecting the PAH
emissions.
The re-evaluation of the Hg test data,
which includes the new test data,
produced a 99-percent UPL of 130 mg/
dscm for existing furnaces producing
FeMn and 12 mg/dscm for existing
furnaces producing SiMn. For new
sources, the new test data did not affect
the 99-percent UPL of 4 mg/dscm for
new furnaces producing SiMn.
With regard to the new source limit in
the supplemental proposal for Hg for
furnaces producing FeMn, the proposed
new source limit was based on BTF
controls using activated carbon injection
(ACI), and assuming 90-percent
reduction. We continue to conclude that
it is appropriate to require BTF controls
for new FeMn sources consistent with
the supplemental proposal (assuming
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90-percent reduction). Therefore, we
calculate that the new source limit for
the final rule for Hg for furnaces
producing FeMn will be 13 m g/dscm
(i.e., 130 m g/dscm minus 90-percent
control). These UPL values are generally
consistent with, but a bit lower than, the
proposed limits in the supplemental
proposal.
3. What key comments did we receive
on the CAA section 112(d)(2) & (3)
proposed revisions, and what are our
responses?
Several comments were received
regarding the CAA section 112(d)(2) &
(3) proposed revisions for the
Ferroalloys Production source category.
The following is a summary of these
comments and our responses. Other
comments received and our responses
can be found in the document titled
National Emission Standards for
Hazardous Air Pollutant Emissions:
Ferroalloys Production Summary of
Public Comments and the EPA’s
Responses on Proposed Rule (76 FR
72508, November 23, 2011) and
Supplemental Proposal (79 FR 60238,
October 6, 2014), which is available in
the docket for this action (EPA–HQ–
OAR–2010–0895).
Comment: Commenters claimed the
EPA was establishing MACT floors for
the newly regulated HAP based on
limited data. The commenters noted
that for many of these pollutants, there
is limited understanding of the
mechanism of their generation in the
process and the variability in the level
of their occurrence. As a result, it is
essential that EPA use all reasonably
available data in establishing these
standards.
The commenters noted the EPA
excluded PAH data for both SiMn and
FeMn production, that showed higher
levels of emissions. They believe the
exclusion of these data led to
calculation of a proposed MACT floor
for PAH that is below the level that can
be demonstrably achieved by the best
performing sources.
The commenters argued that the EPA
should reconsider its decision not to
include these data in calculation of the
MACT floor. One commenter noted that
additional testing to better characterize
variability, particularly for PAH, was
being performed prior to the comment
period for the supplemental proposal
and encouraged the EPA to consider
these additional data in calculating the
MACT floor levels for the final standard.
Response: We have received multiple
test reports from the industry during the
development of the supplemental
proposal and during the comment
period for the supplemental proposal.
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Each test report received was reviewed
to determine if the test met the quality
assurance/quality control (QA/QC)
requirements for this RTR. Only test
data that met these requirements were
used to estimate emissions used for
determining residual risk from the
emissions sources and for determining
the MACT floor limits. Most data we
received passed the QA/QC process and
were judged to be valid data and were
used in our risk analyses and MACT
floor calculations, including data
received shortly before publication of
the supplemental proposal and data
received during the comment period.
The final rule MACT floor limits
include the updated data. However, a
few tests we received previously did not
meet the QA/QC requirements and,
therefore, were not used in these
analyses. For further explanation of the
data evaluation, see the Revised
Development of the Risk and
Technology Review (RTR) Emissions
Dataset for the Ferroalloys Production
Source Category for the 2015 Final Rule
document, which is available in the
docket.
Even though some of the test data
received did not meet the QA/QC
requirements for this RTR, we believe
we still have a robust set of test data for
most of the HAP and the majority of the
MACT floor analyses are based on
multiple tests from each of the facilities.
Comment: One commenter believes
the EPA has not demonstrated that ACI
on new furnaces will provide any
benefits. The commenter notes that the
EPA estimated that Eramet emits only
an estimated 274 pounds of Hg per year,
and Hg emissions do not contribute to
multipathway exposures exceeding an
HQ of 1. Thus, reducing Hg emissions
would not address any existing risks.
If no added cost was involved,
lowering Hg emissions might be a
worthwhile objective. But, the fact is
that cost is a relevant concern under
CAA section 112(d)(2) and, as discussed
below, achieving the proposed new
source standards would be prohibitively
expensive.
The commenter states that the EPA
justifies its conclusion that ACI is
affordable for new sources based on the
assumption that any new source will be
built with a baghouse. As a threshold
matter, the EPA’s assertion that ACI is
cost effective when applied to baghousecontrolled sources is contradicted by its
own supporting memorandum.
According to Table 6–3 of the
Memorandum from Bradley Nelson, EC/
R, Inc. to Phil Mulrine, EPA OAQPS/
SPPD/MICG on Mercury Control
Options and Impacts for the Ferroalloys
Production Industry (Aug. 29, 2014),
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adding ACI is 5 times more expensive
to add to a baghouse than to a scrubber,
and operational costs are 3 times higher.
The table, thus, indicates that the cost
per pound of Hg removed would be
higher, not lower, for EMI’s baghousecontrolled source, and EPA’s estimated
marginal cost is $22,195 per pound,
almost twice the cost presented by the
EPA in the preamble to the 2014
proposal. Since this is based on an
unrealistic removal rate, the unit cost
would actually be at least $44,000 per
pound of Hg removed.
Second, the commenter states that the
sole economic justification for ACI is
the EPA’s substantially understated unit
cost of $17,600 for each pound of Hg
removed. The EPA’s cost-per-pound
metric is completely untethered to any
cost-benefit analysis. To say how much
it will cost to remove a pound of Hg
provides no practical basis for assessing
the relative value of removing that
pound of Hg or the relative ability of a
ferroalloys producer to absorb that cost.
The docket contains no demonstration,
much less substantial evidence, that the
lower cost would nevertheless be
affordable by EMI.
Finally, the commenter notes that the
facility is captive to the pricing
structure imposed by low-cost foreign
ferroalloy producers who will not be
subject to the requirements of this rule.
Accordingly, foreign producers prevent
the facility from passing on costs such
as this to customers via higher prices.
Before that facility can construct a new
furnace, it would have to determine that
the new furnace would produce a
positive return large enough to cover the
cost of constructing and operating that
additional furnace, while charging the
same price charged by producers not
incurring the added costs of ACI. The
EPA provides no explanation for why it
believes this would be possible and our
analysis strongly suggests that it would
not be possible.
The commenter states that the net
result is that the proposed new source
standard effectively prevents EMI from
increasing FeMn production in the
future via a new furnace and ensures
that when the existing furnaces require
replacement, they will not be replaced
with furnaces capable of producing
FeMn. The EPA’s proposed new source
standard is inconsistent with EPA’s
recognition in the 2014 proposal that
EMI is the sole U.S. source of FeMn for
domestic steel production, and its
judgment that ACI should not be
immediately required, in part, because
such a requirement would likely force
EMI out of business. The proposed Hg
‘‘beyond-the-MACT-floor standard’’
produces the same result that the EPA
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agrees should be avoided, only at a later
date.
Response: Activated carbon injection
in conjunction with fabric filter
technology has been successfully used
to reduce emissions of Hg from a
number of different industries. In
addition, the use of brominated carbon
has been used to oxidize the Hg
allowing even greater control
effectiveness for Hg.
The determination of the Hg limits for
new or major reconstructed furnaces is
based on the assurance that such
sources would be constructed to include
a baghouse as the primary PM control
device (in order to comply with the
proposed lower new source limits for
PM) and then they could add ACI after
the baghouse for Hg control along with
a polishing baghouse and would achieve
at least 90-percent reduction of Hg.
In the supplemental proposal, the
estimated costs for beyond the floor
controls for mercury for new and
reconstructed sources were based on the
costs of installing and operating
brominated ACI and a polishing
baghouse. Based on this, in the
supplemental proposal, we estimated
that the cost effectiveness of BTF
controls for a new and major
reconstructed FeMn production source
would be about $12,000/lb. This cost
effectiveness estimate is well within the
range of cost effectiveness levels we
have decided were reasonable in other
rules. Furthermore, no other significant
economic factors were identified that
would indicate that these limits would
be inappropriate or infeasible for new
sources. Therefore, in the supplemental
proposal, we concluded that BTF
controls would be cost-effective and
feasible for any new or major
reconstructed furnace that produces
FeMn.
We received new Hg test data prior to
and during the comment period for the
supplemental proposal. Using these new
test data along with the previous data
we re-evaluated the cost of installing
ACI to reduce Hg. Similar to the
supplemental proposal, we estimated
costs for BTF controls for Hg for new
and reconstructed sources based on the
costs of installing and operating
brominated ACI and a polishing
baghouse. Based on this re-evaluation,
we estimate that the cost effectiveness of
installing ACI for a new and major
reconstructed FeMn production source
would be about $13,600/lb for a furnace
producing FeMn 50 percent of the year,
and $7,100/lb for a furnace producing
FeMn 100 percent of the year.
These cost effectiveness estimates are
similar to the estimate we presented in
the supplemental proposal for the
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beyond the floor option for new FeMn
furnaces and continue to be within the
range of cost effectivenesses we have
determined are reasonable for mercury
control in other rulemakings.
Furthermore, no other significant
economic factors were identified that
would indicate these limits would be
inappropriate or infeasible for new or
major reconstructed furnaces that
produce FeMn. Therefore, we believe
the BTF control option for Hg emissions
is economically and technically feasible
for new and major reconstructed FeMn
furnaces and that these cost
effectivenesses are acceptable for any
new or major reconstructed furnace that
produces FeMn. Additional discussion
of the EPA’s BTF analyses for mercury
are available in the Final Rule Mercury
Control Options and Impacts for the
Ferroalloys Production Industry
document and in the Mercury Control
Options and Impacts for the Ferroalloys
Production Industry document (dated
August 2014) that EPA published in
support of the 2014 supplemental
proposal. These documents are available
in the docket for this action.
An assessment of the cost
effectiveness of emission reductions,
along with other economic factors, is an
appropriate method for assessing cost
impacts in standard setting when CAA
section 112 allows cost to be a factor in
EPA’s decision-making. Nothing in CAA
section 112 compels EPA to use costbenefit analysis in standard-setting
decisions. Moreover, to the extent the
commenter bases its position that the
new source BTF standard for mercury
lacks benefits because it does not
address ‘‘any existing risk,’’ the court of
appeals has held that risk is not a
consideration when setting MACT
standards, as in Sierra Club v. EPA, 353
F.3d 976, 981 (D.C. Cir. 2004). The
emission standards in this rule
discharge EPA’s CAA section 112(d)(2)
duties with respect to Hg emissions
from new and existing electric arc
furnaces in this source category.
4. What is the rationale for our final
approach for the CAA section 112(d)(2)
and (3) revisions?
We evaluated and rejected BTF
options for the CAA section 112(d)(2)
and (3) revisions in the supplemental
proposal and proposed MACT floor
emissions limits for formaldehyde, HCl,
Hg, and PAH for existing sources. We
also evaluated and rejected BTF options
for new sources for formaldehyde, HCl,
and PAHs. For Hg, we also evaluated
BTF options for new furnaces. We
rejected BTF for new SiMn furnaces.
However, we proposed BTF limits for
Hg for FeMn furnaces. See the Revised
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MACT Floor Analysis for the Ferroalloys
Production Source Category document
and the Final Rule Mercury Control
Options and Impacts for the Ferroalloys
Production Industry document, which
are available in the docket.
We are promulgating MACT floorbased limits for the four HAP described
above for existing sources under CAA
section 112(d)(2) and (3) as described
above, which is the same approach as in
the supplemental proposal. Regarding
new sources, we are promulgating
MACT floor limits for new sources for
formaldehyde, HCl, and PAHs, and for
Hg for new SiMn furnaces. However, we
are promulgating a BTF limit for Hg for
FeMn furnaces.
The limits for HCl and formaldehyde
are exactly the same as proposed. The
Hg limits for FeMn and SiMn
production and PAH limits for SiMn
production changed slightly due to the
inclusion of additional data. The only
significant change was for the PAH limit
for FeMn production, which is about 8
times higher than what we proposed. In
our supplemental proposal, we
provided notice of receipt of the highest
test data (i.e., the data received in
August 2014) which when combined
with the other data resulted in a higher
PAH limit. While these data had not
been completely QA/QCed before the
supplemental proposal, both the method
for calculating a limit and most of the
data on which the final limit was
calculated were available and addressed
in the supplemental proposal.
Furthermore, commenters agreed that
the final limit should be based on all
available valid data. As we stated
previously, any changes to the Hg and
PAH emissions limits were a result of
using all of the available valid data
which resulted in a change to the MACT
floor calculations. Additional data
received during the comment period
confirmed a higher PAH limit was
justified.
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D. What changes did we make to the
Ferroalloys Production opacity
monitoring requirement?
1. What changes did we propose for the
ferroalloys production opacity
monitoring requirement?
In the 2014 supplemental proposal,
the EPA solicited comment regarding
the use of new technologies to provide
continuous or near continuous long
term approaches to monitoring
emissions from industrial sources such
as the ferroalloys production facilities
within this source category.
Specifically, we were seeking comment
on the feasibility and practice associated
with the use of automated opacity
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monitoring with ASTM D7520–13,
using DCOT at fixed points to interpret
visible emissions from roof vents
associated with the processes at each
facility, and how this technology could
potentially be included as part of the
requirements in the NESHAP for
ferroalloys production sources.
2. How did the opacity monitoring
requirements change for the Ferroalloys
Production source category?
Based on the information we received
during the comment period for the
supplemental proposal and after further
evaluation of the technology, we believe
that the use of DCOT can provide
opacity readings comparable to Method
9 and reduce the burden of requiring a
person to conduct opacity readings over
the furnace cycle. Furthermore, the
DCOT provides objective and wellsubstantiated readings of opacity. The
DCOT camera provides an image that
the facility could access immediately,
with QA/QC done within 45 minutes to
validate the image and initial readings.
In comparison, it would take a field
observer roughly 30 minutes to return
from the field and average their
manually assembled data such that they
can report the average that they
recorded over the previous 90 minutes
of observations. We view the initial
visible recording as sufficient evidence
to provide the facility enough reason to
initiate, investigate, and correct
concerns that may create elevated visual
emissions observations, and the 45minute turnaround time on actual
opacity values to be quick enough to
provide a facility the confirmation they
would need to be assured that they have
taken appropriate action.
3. What key comments did we receive
on the opacity monitoring requirement,
and what are our responses?
Comment: In their supplemental
proposal comments, one commenter
objects to the significantly increased
frequency of opacity observations from
once every 5 years to weekly. They note
that the Agency states that the frequency
is ‘‘appropriate’’ to demonstrate
compliance with the process fugitive
standard with the enhanced frequency
presumably substituting for the
continuous negative pressure
monitoring obligations from the 2011
proposal.
The commenter believes that this
explanation overlooks the stringent
continuous monitoring that the
proposed rule already requires to ensure
that the process fugitives control system
meets the 95-percent capture
requirement. First, the facility must
develop a plan to demonstrate 95-
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percent capture, and that plan must be
approved by the permitting authority.
Next, the facility must perform an initial
compliance demonstration. The facility
must then identify specific parameters,
either through the engineering
assessment or the initial compliance
demonstration, that are indicative of
compliance with the opacity standard.
Finally, on an ongoing basis, the facility
must routinely monitor those
parameters.
The commenter notes that an initial
compliance demonstration and ongoing
monitoring is a standard regulatory
approach required in any number of
MACT standards. However, none of
these other standards require weekly
testing to confirm that the parameters
and limits are still being met and many
other standards require re-testing only
every 5 years, or at most annually. They
believe that nothing in the current
proposal demonstrates why it is
necessary or appropriate to deviate from
this standard approach here.
Two commenters believe that the
proposed weekly opacity testing will
impose significant ongoing costs on the
facilities for no additional
environmental benefit. They believe that
the ongoing parametric monitoring is
sufficient to ensure compliance on an
ongoing basis.
These commenters believe that the
weekly opacity reading requirement is
overly burdensome, especially for
Eramet because they have three shop
buildings. They estimate 3–5 hours per
building opacity reading for a total of 9–
15 hours a week for reading opacity.
Response: We re-evaluated the
opacity monitoring requirements in the
supplemental proposal and determined
that the DCOT and ASTM D7520–13
provided a development that ensures
compliance with the fugitive emissions
standards, as well as reduces the labor
burden on the facilities. After initial
setup, the DCOT can measure the
opacity during the furnace process cycle
without any labor needed. In addition,
facilities would not have the cost of
annual certification as is the case with
Method 9. We estimate that the overall
costs of DCOT and ASTM D7520–13
will be approximately the same as what
the overall costs would be if facilities
used method 9. In addition, due to the
baseline unacceptable risk finding being
based largely on process fugitive
manganese emissions, we believe the
frequent opacity readings using the
objective and substantiated results of
DCOT are warranted to ensure fugitive
emissions are effectively captured and
controlled. However, after considering
comments, we decided to allow
facilities an opportunity to reduce the
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frequency of opacity readings to once
per month per furnace building (instead
of weekly) if the facility achieves 26
consecutive compliant weekly readings
for that furnace building. This reduction
in frequency will reduce the cost burden
for the facilities. However, if any of the
subsequent monthly readings exceed the
opacity limit for that furnace building,
the facility must return to weekly
readings until they achieve another 26
compliant weekly readings, at which
time the facility can return to monthly
readings.
Comment: One commenter supported
the EPA’s determination that opacity
observations should be measured over a
furnace process cycle. However, because
all furnaces at the Felman facility are
located in the same building, the
commenter suggests treating the
building as a single opacity source, and
that opacity observations be conducted
over a time period that captures a full
furnace process cycle from each furnace
within that building.
Response: We agree with the
commenter and have revised the opacity
requirements to include opacity
determinations from buildings with
multiple furnaces. The requirement will
treat the building with multiple
furnaces as a single opacity source and
the opacity readings will be conducted
over a time period that will include
tapping from each of the furnaces in
operation.
Comment: In comments on the
supplemental proposal, two
commenters state that the EPA should
require the use of the best available
testing method, digital opacity
monitoring. The commenters describe
the benefits of the DCOT compared to
Method 9 and provide supporting
documentation. In particular, one
commenter supports the DCOT because
it is EPA certified as a valid test method
for opacity and approved for its use, the
use of a camera creates a good electronic
record of the observations, conditions,
location, etc., and a number of regulated
entities are using this method to assess
opacity. The commenter adds that using
cameras can save resources, citing a
Department of Defense project to reduce
Method 9 certification costs. The
commenter adds that the EPA should
also require opacity determinations to
be documented on an electronic form
and provided on the Internet in real
time for public review.
One commenter adds that the EPA
should not allow Method 9 to be used,
unless there is a power outage requiring
the facility to use Method 9 to assure
opacity standard compliance. They also
add that instead of Method 9, the EPA
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should require a source to use either
continuous opacity monitor or DCOT.
Response: We evaluated the use of
DCOT and the ASTM D7520–13 method
and determined that this technology
provides the same compliance
assurance as Method 9 measurements
with approximately the same overall
burden on the facilities and the DCOT
provides reliable, unbiased opacity
readings. Therefore, we are requiring
opacity determinations to be made using
DCOT and ASTM D7520–13. With
regard to the comment suggesting that
the DCOT results be documented in an
electronic format and provided on the
internet in real time, the DCOT results
will be recorded in an electronic format.
Furthermore, use of the DCOT will
improve transparency of opacity
monitoring results. However, we do not
have a system established to provide
these results on the internet in real time.
Furthermore, the ERT is not yet
configured to be able to accept the
DCOT compliance images. Nevertheless,
the rule requires the affected sources to
maintain electronic records of the DCOT
results and submit periodic compliance
monitoring reports to the Administrator
or permit authority. We believe that the
public will be able to obtain copies of
the compliance results within a
reasonable amount of time by contacting
the EPA and/or the permit authority
through the appropriate channels.
Comment: One commenter requests a
clarification to the proposed regulatory
language: That EPA add the phrase
‘‘over a furnace process cycle’’ at the
end of 40 CFR 63.1623(b)(3). As written
in the supplemental proposal, the
language requires that opacity emissions
not exceed 8 percent, but no averaging
time is specified. The proposed
subsections, § 63.1623(b)(3)(i) though
(iii) stated that the compliance
demonstration for this obligation must
be determined over the course of an
entire furnace process cycle, but they do
not clearly state that the limit itself is 8
percent over the entire furnace process
cycle, and not, for example, an
instantaneous limit, or 8 percent over a
6-minute period. To avoid
misunderstanding, this averaging period
should be stated clearly as part of the
standard itself.
Response: We agree with the
commenter and have included language
that clarifies the opacity requirement in
the final rule.
4. What is the rationale for our final
decision for the opacity monitoring
requirement?
We are finalizing requirements to
measure opacity from the furnace
buildings using ASTM D7520–13 and
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digital camera technology because we
conclude this is the best method to
ensure reliable and unbiased readings
for opacity. We are also finalizing the
requirement that facilities need to meet
an average opacity standard of no more
than 8-percent opacity for each furnace
cycle. Furthermore, we are finalizing the
requirement that at no time during
operation may any two consecutive 6minute block opacity readings (12minute period) be greater than 20percent opacity.
V. Summary of Cost, Environmental,
and Economic Impacts and Additional
Analyses Conducted
A. What are the affected facilities?
Eramet Marietta Incorporated, in
Marietta, Ohio and Felman Production
LLC, in Letart West Virginia, are the 2
manganese ferroalloys production
facilities currently operating in the
United States that will be affected by
these amendments. We do not know of
any new facilities that are expected to
be constructed in the foreseeable future.
However, there is one other facility that
has a permit to produce FeMn or SiMn
in an electric arc furnace, but it is not
doing so at present. It is possible,
however, that this facility could resume
production or another non-manganese
ferroalloy producer could decide to
commence production of FeMn or
SiMn. Given this uncertainty, our
impact analysis is focused on the two
existing sources that are currently
operating.
B. What are the air quality impacts?
As noted in the 2011 proposal,
emissions of metal HAP from ferroalloys
production sources have declined in
recent years, primarily as the result of
state actions and also due to the
industry’s own initiative. The final
amendments in this rule would cut HAP
emissions (primarily particulate metal
HAP such as manganese, arsenic, and
nickel) by about 60 percent from their
current levels. Under the final emissions
standards for process fugitives
emissions from the furnace building, we
estimate that the HAP emissions
reductions would be 77 tpy, including
significant reductions of manganese.
C. What are the cost impacts?
Under the revised final amendments,
each ferroalloys production facility is
expected to incur costs for the design,
installation and operation of an
enhanced local capture system. Each
facility also is expected to incur costs
associated with the installation of
additional control devices to manage the
air flows generated by the enhanced
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capture systems. There would also be
capital costs associated with installing
new or improved continuous
monitoring systems, including
installation of BLDS on the furnace
baghouses that are not currently
equipped with these systems and
installation and operation of DCOT
systems to monitor opacity.
The revised capital costs for each
facility were estimated based on the
projected number and types of upgrades
required. The specific enhancements for
each facility were selected for cost
estimation based on estimates directly
provided by the facilities based on their
engineering analyses and discussions
with the EPA. The Cost Impacts of
Control Options to Address Fugitive
HAP Emissions for the Ferroalloys
Production NESHAP Supplemental
Proposal document includes a complete
description of the revised cost estimate
methods used for this analysis and is
available in the docket.
Cost elements vary by plant and
furnace and include the following
elements:
• Curtains or doors surrounding
furnace tops to contain fugitive
emissions;
• Improvements to hoods collecting
tapping emissions;
• Upgraded fans to improve the
airflow of fabric filters controlling
fugitive emissions;
• Addition of ‘‘secondary capture’’ or
additional hoods to capture emissions
from tapping platforms or crucibles;
• Addition of fugitives capture for
casting operations;
• Improvement of existing control
devices or addition of fabric filters; and
• Addition of rooftop ventilation, in
which fugitive emissions escaping local
control are collected in the roof canopy
over process areas through addition of
partitions and hoods, then directed
through roof vents and ducts to control
devices.
For purposes of the analysis for the
final rule, we assumed that enhanced
capture systems and roofline ventilation
will be installed for all operational
furnaces at both facilities and for MOR
operations at Eramet Marietta. The
specific elements of the capture and
control systems selected for each facility
are based on information supplied by
the facilities incorporating their best
estimates of the improvements to
fugitive emission capture and control
they would implement to achieve the
standards included in the final rule. We
estimate the total capital costs of
installing the required ductwork, fans,
control devices, and monitoring to
comply with the enhanced capture
system requirements to be $40.3 million
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and the total annualized cost to be $7.7
million (2012 dollars) for the two plants.
We estimate that enhanced capture and
control systems required by this rule
will reduce metal HAP emissions by 75
tons, resulting in a cost per ton of metal
HAP removed to be $106,000 per ton
($53 per pound). The total HAP
reduction for the enhanced capture and
control systems is estimated to be 77 tpy
at a cost per ton of $103,000 per ton
($52 per pound). We also estimate that
these systems will achieve PM emission
reductions of 229 tpy, resulting in cost
per ton of PM removed of $34,600 per
ton and achieve PM2.5 emission
reductions of 48 tpy, resulting in a cost
per ton of PM2.5 removal of $165,000 per
ton.
D. What are the economic impacts?
As a result of the requirements in this
final rule, we estimate that the total
capital cost for the Eramet facility will
be about $25.4 million and the total
annualized costs will be about $5.6
million (in 2012 dollars). For impacts to
Felman Production LLC, this facility is
estimated to incur a total capital cost of
$14.9 million and a total annualized
costs of just under $2.1 million (in 2012
dollars). In total, these costs could lead
to an increase in annualized cost of
about 1.9 percent of sales, which serves
as an estimate for the increase in
product prices, and a decrease in output
of as much as 10.1 percent. For more
information regarding economic
impacts, please refer to the Economic
Impact Analysis report and the
summary of public comments and EPA’s
responses document which are included
in the public docket for this final rule.
E. What are the benefits?
The estimated reductions in HAP
emissions (i.e., about 77 tpy) that will be
achieved by this action will provide
significant benefits to public health. For
example, there will be a significant
reduction in emissions of HAP metals
(especially manganese, arsenic, nickel,
chromium, cadmium, and lead). The
rule will also achieve some reductions
of Hg and PAHs. In addition to the HAP
reductions, we also estimate that this
final rule will reduce 48 tons in PM2.5
emissions as a co-benefit of the HAP
reductions annually.
This rulemaking is not an
‘‘economically significant regulatory
action’’ under Executive Order 12866
because it is not likely to have an
annual effect on the economy of $100
million or more. Therefore, we have not
conducted a Regulatory Impact Analysis
(RIA) for this rulemaking or a benefits
analysis. While we expect that these
avoided emissions will result in
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improvements in air quality and reduce
health effects associated with exposure
to HAP associated with these emissions,
we have not quantified or monetized the
benefits of reducing these emissions for
this rulemaking. This does not imply
that there are no benefits associated
with these emission reductions. In fact,
our demographic analysis indicates that
thousands of people live within 50
kilometers of these two facilities and
these people will experience benefits
because of the reduced exposure to air
toxics due to this rulemaking.
When determining if the benefits of
an action exceed its costs, Executive
Orders 12866 and 13563 direct the
Agency to consider qualitative benefits
that are difficult to quantify but
essential to consider. Controls installed
to reduce HAP would also reduce
ambient concentrations of PM2.5 as a cobenefit. Reducing exposure to PM2.5 is
associated with significant human
health benefits, including avoided
premature mortality and morbidity from
cardiovascular and respiratory illnesses.
Researchers have associated PM2.5
exposure with adverse health effects in
numerous toxicological, clinical and
epidemiological studies (U.S. EPA,
2009).4 When adequate data and
resources are available and an RIA is
required, the EPA generally quantifies
several health effects associated with
exposure to PM2.5 (U.S. EPA, 2012).5
These health effects include premature
mortality for adults and infants,
cardiovascular morbidities such as heart
attacks, hospital admissions and
respiratory morbidities such as asthma
attacks, acute bronchitis, hospital and
emergency department visits, work loss
days, restricted activity days, and
respiratory symptoms. The scientific
literature also suggests that exposure to
PM2.5 is also associated with adverse
effects on birth weight, pre-term births,
pulmonary function and other
cardiovascular and respiratory effects
(U.S. EPA, 2009), but the EPA has not
quantified certain outcomes of these
impacts in its benefits analyses. PM2.5
also increases light extinction, which is
4 U.S. Environmental Protection Agency (U.S.
EPA). 2009. Integrated Science Assessment for
Particulate Matter (Final Report). EPA–600–R–08–
139F. National Center for Environmental
Assessment—RTP Division. Available on the
Internet at https://cfpub.epa.gov/ncea/cfm/
recordisplay.cfm?deid=216546.
5 U.S. Environmental Protection Agency (U.S.
EPA). 2012. Regulatory Impact Analysis for the
Proposed Revisions to the National Ambient Air
Quality Standards for Particulate Matter. Office of
Air and Radiation, Research Triangle Park, NC.
Available on the Internet at https://www.epa.gov/
ttnecas1/regdata/RIAs/PMRIACombinedFile_
Bookmarked.pdf.
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an important aspect of reduced
visibility.
The rulemaking is also anticipated to
reduce emissions of other HAP,
including metal HAP (arsenic,
cadmium, chromium (both total and
hexavalent), lead compounds,
manganese, and nickel) and PAHs.
Some of these HAP are carcinogenic
(e.g., arsenic, PAHs) and some are toxic
and have effects other than cancer (e.g.,
kidney disease from cadmium,
respiratory, and immunological effects
from nickel). While we cannot
quantitatively estimate the benefits
achieved by reducing emissions of these
HAP, qualitative benefits are expected
as a result of reducing exposures to
these HAP. More information about the
health effects of these HAP can be found
on the IRIS,6 ATSDR,7 and California
EPA 8 Web pages.
F. What analysis of environmental
justice did we conduct?
As explained in section IV.A of this
preamble, we assessed the impacts to
various demographic groups. The
methodology and the results of the
analyses are described in the Risk and
Technology Review—Analysis of SocioEconomic Factors for Populations Living
Near Ferroalloys Facilities, which is
available in the docket.
Based on that assessment, we
conclude that this final rule will reduce
the number of people exposed to
elevated risks, from approximately
41,000, to about 26,000 people exposed
to a potential cancer risk greater than or
equal to 1-in-1 million and from 1,300
to zero people exposed to a potential
chronic noncancer hazard level of 1.
Based on this analysis, the EPA has
determined that these final rule
requirements will not have
disproportionately high and adverse
human health or environmental effects
on minority or low-income populations
because it increases the level of
environmental protection for all affected
populations. See Section VI.J of this
preamble for more information.
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G. What analysis of children’s
environmental health did we conduct?
This action is not subject to Executive
Order 13045 (62 FR 19885, April 23,
1997) because the Agency does not
believe the environmental health risks
6 U.S. EPA, 2006. Integrated Risk Information
System. https://www.epa.gov/iris/.
7 U.S. Agency for Toxic Substances and Disease
Registry, 2006. Minimum Risk Levels (MRLs) for
Hazardous Substances. https://www.atsdr.cdc.gov/
mrls/.
8 CA Office of Environmental Health Hazard
Assessment, 2005. Chronic Reference Exposure
Levels Adopted by OEHHA as of December 2008.
https://www.oehha.ca.gov/air/chronic_rels.
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or safety risks addressed by this action
present a disproportionate risk to
children. The report, Analysis of SocioEconomic Factors for Populations Living
Near Ferroalloys Facilities, which is
available in the docket, shows that,
prior to the implementation of the
provisions included in this final rule, on
a nationwide basis, there are
approximately 41,000 people exposed to
a cancer risk at or above 1-in-1 million
and approximately 1,300 people
exposed to a chronic noncancer TOSHI
greater than 1 due to emissions from the
source category. The percentages for all
demographic groups (with the exception
of those ages 65 and older, which is
only slightly higher than the national
average), including children 18 years
and younger, are similar to or lower
than their respective nationwide
percentages. Further, implementation of
the provisions included in this action is
expected to significantly reduce the
number of at-risk people due to HAP
emissions from these sources (from
approximately 41,000 to about 26,000
for cancer risks and from 1,300 to zero
for chronic noncancer hazards),
providing significant benefit to all
demographic groups.
This rule is expected to reduce
environmental impacts for everyone,
including children. This action
establishes emissions limits at the levels
based on MACT, as required by the
CAA. Based on our analysis, we believe
that this rule does not present a
disproportionate risk to children
because it increases the level of
environmental protection for all affected
populations.
VI. Statutory and Executive Order
Reviews
Additional information about these
statutes and Executive Orders can be
found at https://www2.epa.gov/lawsregulations/laws-and-executive-orders.
A. Executive Orders 12866: Regulatory
Planning and Review and Executive
Order 13563: Improving Regulation and
Regulatory Review
This action is not a significant
regulatory action and was, therefore, not
submitted to the Office of Management
and Budget (OMB) for review.
B. Paperwork Reduction Act (PRA)
The information collection activities
in this rule have been submitted for
approval to the OMB under the PRA.
The ICR document that the EPA
prepared has been assigned EPA ICR
number 2488.01. You can find a copy of
the ICR in the docket for this rule, and
it is briefly summarized here. The
information collection requirements are
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not enforceable until OMB approves
them.
The information requirements in this
rulemaking are based on the
notification, recordkeeping, and
reporting requirements in the NESHAP
General Provisions (40 CFR part 63,
subpart A), which are mandatory for all
operators subject to national emission
standards. These notifications, reports,
and records are essential in determining
compliance, and are specifically
authorized by CAA section 114 (42
U.S.C. 7414). All information submitted
to the EPA pursuant to the
recordkeeping and reporting
requirements for which a claim of
confidentiality is made is safeguarded
according to agency policies set forth in
40 CFR part 2, subpart B.
Respondents/affected entities: New
and existing ferroalloys production
facilities that produce FeMn and SiMn
and are either major sources of HAP
emissions or are co-located at major
sources of HAP.
Respondent’s obligation to respond:
Mandatory (42 U.S.C. 7414).
Estimated number of respondents: 2.
Frequency of response: Semiannual.
Total estimated burden: 707 hours
(per year). Burden is defined at 5 CFR
1320.3(b).
Total estimated cost: $0.85 million
(per year), includes $0.78 million
annualized capital or operation &
maintenance costs.
An agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid OMB
control number. The OMB control
numbers for the EPA’s regulations in 40
CFR are listed in 40 CFR part 9. When
OMB approves this ICR, the agency will
announce that approval in the Federal
Register and publish a technical
amendment to 40 CFR part 9 to display
the OMB control number for the
approved information collection
activities contained in this final rule.
C. Regulatory Flexibility Act (RFA)
I certify that this action will not have
a significant economic impact on a
substantial number of small entities
under the RFA. The small entities
subject to the requirements of this
action are businesses that can be
classified as small firms using the Small
Business Administration size standards
for their respective industries. The
agency has determined that neither of
the companies affected by this rule is
considered to be a small entity. Details
of this analysis are presented in the
memorandum, Economic Impact
Analysis for Risk and Technology
Review: Ferroalloys Production Source
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Category, which is available in the
docket for this action.
D. Unfunded Mandates Reform Act
(UMRA)
This action does not contain an
unfunded mandate of $100 million or
more as described in UMRA, 2 U.S.C.
1531–1538, and does not significantly or
uniquely affect small governments. The
action imposes no enforceable duty on
any state, local, or tribal governments,
or on the private sector.
E. Executive Order 13132: Federalism
This action does not have federalism
implications. It will not have substantial
direct effects on the states, on the
relationship between the national
government and the states, or on the
distribution of power and
responsibilities among the various
levels of government.
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
This action does not have tribal
implications as specified in Executive
Order 13175. There are no ferroalloys
production facilities that are owned or
operated by 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
This action is not subject to Executive
Order 13045 because it is not
economically significant as defined in
Executive Order 12866, and because the
EPA does not believe the environmental
health or safety risks addressed by this
action present a disproportionate risk to
children. This action’s health and risk
assessments are contained in the
Residual Risk Assessment for the
Ferroalloys Production Source Category
in Support of the 2015 Risk and
Technology Review Final Rule
document, which is available in the
docket for this action, and are discussed
in section V.G of this preamble.
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H. Executive Order 13211: Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution or Use
This action is not subject to Executive
Order 13211 because it is not a
significant regulatory action under
Executive Order 12866.
I. National Technology Transfer and
Advancement Act and 1 CFR Part 51
This final rule involves technical
standards. EPA decided to use ASME
PTC 19.10–1981, ‘‘Flue and Exhaust Gas
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Analyses,’’ for its manual methods of
measuring the oxygen or carbon dioxide
content of the exhaust gas. These parts
of ASME PTC 19.10–1981 are acceptable
alternatives to EPA Method 3B. This
standard is available from the American
Society of Mechanical Engineers
(ASME), Three Park Avenue, New York,
NY 10016–5990.
The EPA has also decided to use
ASTM D7520–13, Standard Test Method
for Determining the Opacity in a Plume
in an Outdoor Ambient Atmosphere, for
measuring opacity from the shop
buildings. This standard is an
acceptable alternative to EPA Method 9
and is available from the American
Society for Testing and Materials
(ASTM), 100 Barr Harbor Drive, Post
Office Box C700, West Conshohocken,
PA 19428–2959. See https://
www.astm.org/.
In addition, the EPA has decided to
use California Air Resources Board
Method 429, Determination of
Polycyclic Aromatic Hydrocarbon
(PAH) Emissions from Stationary
Sources for measuring PAH emissions
from the furnace control device. This
method is an acceptable alternative to
EPA Method 0010 and is available from
the California Air Resources Board
(CARB), Engineering and Certification
Branch, 1001 I Street, P.O. Box 2815,
Sacramento, CA 95812–2815. See
https://www.arb.ca.gov/testmeth/vol3/M_
429.pdf.
The EPA has also decided to use EPA
Methods 1, 2, 3A, 3B, 4, 5, 5D, 10, 26A,
29, 30B, 316 of 40 CFR part 60,
appendix A. No applicable VCS were
identified for EPA Methods 30B, 5D,
316.
Under 40 CFR 63.7(f) and 40 CFR
63.8(f) of subpart A of the 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 this
final rule.
J. Executive Order 12898: Federal
Actions To Address Environmental
Justice in Minority Populations and
Low-Income Populations
The EPA has determined that the
current health risks posed by emissions
from this source category are
unacceptable. There are up to 41,000
people living in close proximity to the
two facilities that are currently subject
to health risks which may not be
considered negligible (i.e., cancer risks
greater than 1-in-1 million or chronic
noncancer TOSHI greater than 1) due to
emissions from this source category.
The demographic makeup of this
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population is similar to the national
distribution for all demographic groups,
with the exception of those ages 65 and
older, which is slightly higher than the
national average. This final rule will
reduce the number of people in this
group, from approximately 41,000, to
about 26,000 people exposed to a cancer
risk greater than or equal to 1-in-1
million and from 1,300 to zero people
for a chronic noncancer hazard index of
1. The EPA believes the human health
or environmental risk addressed by this
action will not have potential
disproportionately high and adverse
human health or environmental effects
on minority, low-income, or indigenous
populations because it increases the
level of environmental protection for all
affected populations. The results of this
evaluation are contained in section IV.A
of this preamble. A copy of this
methodology and the results of the
demographic analysis are included in a
technical report, Risk and Technology
Review—Analysis of Socio-Economic
Factors for Populations Living Near
Ferroalloys Facilities, which is available
in the docket for this action.
K. Congressional Review Act (CRA)
This action is subject to the CRA, and
the EPA will submit a rule report to
each House of the Congress and to the
Comptroller General of the United
States. This action is not a ‘‘major rule’’
as defined by 5 U.S.C. 804(2).
List of Subjects for 40 CFR Part 63
Environmental protection,
Administrative practice and procedures,
Air pollution control, Hazardous
substances, Incorporation by reference,
Intergovernmental relations, Reporting
and recordkeeping requirements.
Dated: May 28, 2015.
Gina McCarthy,
Administrator.
For the reasons stated in the
preamble, the Environmental Protection
Agency is amending title 40, chapter I,
part 63 of the Code of Federal
Regulations (CFR) as follows:
PART 63—NATIONAL EMISSION
STANDARDS FOR HAZARDOUS AIR
POLLUTANTS FOR SOURCE
CATEGORIES
1. The authority citation for part 63
continues to read as follows:
■
Authority: 42 U.S.C. 7401 et seq.
Subpart A—General Provisions
■
■
2. Section 63.14 is amended:
a. By revising paragraph (f)(1);
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b. By redesignating paragraphs (g)(87)
through (94) as paragraphs (g)(88)
through (95), respectively;
■ c. By adding new paragraph (g)(87);
■ d. By revising paragraph (j)
introductory text;
■ e. By redesignating paragraphs (j)(1)
through (3) as paragraphs (j)(2) through
(4), respectively; and
■ f. By adding new paragraph (j)(1).
The revisions and additions read as
follows:
63.1624 What are the operational and work
practice standards for new,
reconstructed, and existing facilities?
63.1625 What are the performance test and
compliance requirements for new,
reconstructed, and existing facilities?
63.1626 What monitoring requirements
must I meet?
63.1627 What notification requirements
must I meet?
63.1628 What recordkeeping and reporting
requirements must I meet?
63.1629 Who implements and enforces this
subpart?
§ 63.14
*
■
Incorporations by reference.
*
*
*
*
*
(f) * * *
(1) ANSI/ASME PTC 19.10–1981,
Flue and Exhaust Gas Analyses [Part 10,
Instruments and Apparatus], issued
August 31, 1981, IBR approved for
§§ 63.309(k), 63.457(k), 63.772(e) and
(h), 63.865(b), 63.1282(d) and (g),
63.1625(b), 63.3166(a), 63.3360(e),
63.3545(a), 63.3555(a), 63.4166(a),
63.4362(a), 63.4766(a), 63.4965(a),
63.5160(d), table 4 to subpart UUUU,
63.9307(c), 63.9323(a), 63.11148(e),
63.11155(e), 63.11162(f), 63.11163(g),
63.11410(j), 63.11551(a), 63.11646(a),
and 63.11945, table 5 to subpart
DDDDD, table 4 to subpart JJJJJ, tables 4
and 5 of subpart UUUUU, and table 1
to subpart ZZZZZ.
*
*
*
*
*
(g) * * *
(87) ASTM D7520–13, ‘‘Standard Test
Method for Determining the Opacity in
a Plume in an Outdoor Ambient
Atmosphere,’’ Approved December 1,
2013, IBR approved for §§ 63.1625(b).
*
*
*
*
*
(j) California Air Resources Board
(CARB), 1001 I Street, P.O. Box 2815,
Sacramento, CA 95812–2815, Telephone
(916) 327–0900, https://www.arb.ca.gov/.
(1) Method 429, Determination of
Polycyclic Aromatic Hydrocarbon
(PAH) Emissions from Stationary
Sources, Adopted September 12, 1989,
Amended July 28, 1997, IBR approved
for § 63.1625(b).
*
*
*
*
*
Subpart XXX—National Emission
Standards for Hazardous Air Pollutants
for Ferroalloys Production:
Ferromanganese and Silicomanganese
3. Sections 63.1620 through 63.1629
are added to read as follows:
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■
Sec.
63.1620 Am I subject to this subpart?
63.1621 What are my compliance dates?
63.1622 What definitions apply to this
subpart?
63.1623 What are the emissions standards
for new, reconstructed and existing
facilities?
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*
§ 63.1620
*
*
*
Am I subject to this subpart?
(a) You are subject to this subpart if
you own or operate a new or existing
ferromanganese and/or silicomanganese
production facility that is a major source
or is co-located at a major source of
hazardous air pollutant emissions.
(b) You are subject to this subpart if
you own or operate any of the following
equipment as part of a ferromanganese
and/or silicomanganese production
facility:
(1) Electric arc furnace;
(2) Casting operations;
(3) Metal oxygen refining (MOR)
process;
(4) Crushing and screening
operations;
(5) Outdoor fugitive dust sources.
(c) A new affected source is any of the
equipment listed in paragraph (b) of this
section for which construction or
reconstruction commenced after June
30, 2015.
(d) Table 1 of this subpart specifies
the provisions of subpart A of this part
that apply to owners and operators of
ferromanganese and silicomanganese
production facilities subject to this
subpart.
(e) If you are subject to the provisions
of this subpart, you are also subject to
title V permitting requirements under 40
CFR part 70 or 71, as applicable.
(f) Emission standards in this subpart
apply at all times.
§ 63.1621
What are my compliance dates?
(a) Existing affected sources must be
in compliance with the provisions
specified in §§ 63.1620 through 63.1629
no later than June 30, 2017.
(b) Affected sources in existence prior
to June 30, 2015 must be in compliance
with the provisions specified in
§§ 63.1650 through 63.1661 by
November 21, 2001 and until June 30,
2017. As of June 30, 2017, the
provisions of §§ 63.1650 through
63.1661 cease to apply to affected
sources in existence prior to June 30,
2015. The provisions of §§ 63.1650
through 63.1661 remain enforceable at a
source for its activities prior to June 30,
2017.
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(c) If you own or operate a new
affected source that commences
construction or reconstruction after
November 23, 2011, you must comply
with the requirements of this subpart by
June 30, 2015, or upon startup of
operations, whichever is later.
§ 63.1622
subpart?
What definitions apply to this
Terms in this subpart are defined in
the Clean Air Act (Act), in subpart A of
this part, or in this section as follows:
Bag leak detection system means a
system that is capable of continuously
monitoring particulate matter (dust)
loadings in the exhaust of a baghouse in
order to detect bag leaks and other upset
conditions. A bag leak detection system
includes, but is not limited to, an
instrument that operates on
triboelectric, light scattering, light
transmittance, or other effect to
continuously monitor relative
particulate matter loadings.
Capture system means the collection
of components used to capture the gases
and fumes released from one or more
emissions points and then convey the
captured gas stream to a control device
or to the atmosphere. A capture system
may include, but is not limited to, the
following components as applicable to a
given capture system design: Duct
intake devices, hoods, enclosures,
ductwork, dampers, manifolds,
plenums, fans and roofline ventilation
systems.
Casting means the period of time from
when molten ferroalloy is removed from
the tapping station until the pouring
into casting molds or beds is completed.
This includes the following operations:
Pouring alloy from one ladle to another,
slag separation, slag removal and ladle
transfer by crane, truck, or other
conveyance.
Crushing and screening equipment
means the crushers, grinders, mills,
screens and conveying systems used to
crush, size and prepare for packing
manganese-containing materials,
including raw materials, intermediate
products and final products.
Electric arc furnace means any
furnace where electrical energy is
converted to heat energy by
transmission of current between
electrodes partially submerged in the
furnace charge. The furnace may be of
an open, semi-sealed, or sealed design.
Furnace process cycle means the
period in which the furnace is tapped to
the time in which the furnace is tapped
again and includes periods of charging,
smelting, tapping, casting and ladle
raking. For multiple furnaces operating
within a single shop building, furnace
process cycle means a period sufficient
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to capture a full cycle of charging,
smelting, tapping, casting and ladle
raking for each furnace within the shop
building.
Ladle treatment means a post-tapping
process including metal and alloy
additions where chemistry adjustments
are made in the ladle after furnace
smelting to achieve a specified product.
Local ventilation means hoods,
ductwork, and fans designed to capture
process fugitive emissions close to the
area where the emissions are generated
(e.g., tap hoods).
Metal oxygen refining (MOR) process
means the reduction of the carbon
content of ferromanganese through the
use of oxygen.
Outdoor fugitive dust source means a
stationary source from which hazardous
air pollutant-bearing particles are
discharged to the atmosphere due to
wind or mechanical inducement such as
vehicle traffic. Fugitive dust sources
include plant roadways, yard areas and
outdoor material storage and transfer
operation areas.
Plant roadway means any area at a
ferromanganese and silicomanganese
production facility that is subject to
plant mobile equipment, such as
forklifts, front end loaders, or trucks,
carrying manganese-bearing materials.
Excluded from this definition are
employee and visitor parking areas,
provided they are not subject to traffic
by plant mobile equipment.
Process fugitive emissions source
means a source of hazardous air
pollutant emissions that is associated
with a ferromanganese or
silicomanganese production facility and
is not a fugitive dust source or a stack
emissions source. Process fugitive
sources include emissions that escape
capture from the electric arc furnace,
tapping operations, casting operations,
ladle treatment, MOR or crushing and
screening equipment.
Roofline ventilation system means an
exhaust system designed to evacuate
process fugitive emissions that collect in
the roofline area to a control device.
Shop building means the building
which houses one or more electric arc
furnaces or other processes that generate
process fugitive emissions.
Shutdown means the cessation of
operation of an affected source for any
purpose.
Startup means the setting in operation
of an affected source for any purpose.
Tapping emissions means the gases
and emissions associated with removal
of product from the electric arc furnace
under normal operating conditions,
such as removal of metal under normal
pressure and movement by gravity
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down the spout into the ladle and filling
the ladle.
Tapping period means the time from
when a tap hole is opened until the time
a tap hole is closed.
§ 63.1623 What are the emissions
standards for new, reconstructed and
existing facilities?
(a) Electric arc furnaces. You must
install, operate and maintain an
effective capture system that collects the
emissions from each electric arc furnace
operation and conveys the collected
emissions to a control device for the
removal of the pollutants specified in
the emissions standards specified in
paragraphs (a)(1) through (5) of this
section.
(1) Particulate matter emissions. (i)
You must not discharge exhaust gases
from each electric arc furnace operation
containing particulate matter in excess
of 4.0 milligrams per dry standard cubic
meter (mg/dscm) into the atmosphere
from any new or reconstructed electric
arc furnace.
(ii) You must not discharge exhaust
gases from each electric arc furnace
operation containing particulate matter
in excess of 25 mg/dscm into the
atmosphere from any existing electric
arc furnace.
(2) Mercury emissions. (i) You must
not discharge exhaust gases from each
electric arc furnace operation containing
mercury emissions in excess of 13
micrograms per dry standard cubic
meter (mg/dscm) into the atmosphere
from any new or reconstructed electric
arc furnace when producing
ferromanganese.
(ii) You must not discharge exhaust
gases from each electric arc furnace
operation containing mercury emissions
in excess of 130 mg/dscm into the
atmosphere from any existing electric
arc furnace when producing
ferromanganese.
(iii) You must not discharge exhaust
gases from each electric arc furnace
operation containing mercury emissions
in excess of 4 mg/dscm into the
atmosphere from any new or
reconstructed electric arc furnace when
producing silicomanganese.
(iv) You must not discharge exhaust
gases from each electric arc furnace
operation containing mercury emissions
in excess of 12 mg/dscm into the
atmosphere from any existing electric
arc furnace when producing
silicomanganese.
(3) Polycyclic aromatic hydrocarbon
emissions. (i) You must not discharge
exhaust gases from each electric arc
furnace operation containing polycyclic
aromatic hydrocarbon emissions in
excess of 12,000 mg/dscm into the
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atmosphere from any new or
reconstructed electric arc furnace when
producing ferromanganese.
(ii) You must not discharge exhaust
gases from each electric arc furnace
operation containing polycyclic
aromatic hydrocarbon emissions in
excess of 12,000 mg/dscm into the
atmosphere from any existing electric
arc furnace when producing
ferromanganese.
(iii) You must not discharge exhaust
gases from each electric arc furnace
operation containing polycyclic
aromatic hydrocarbon emissions in
excess of 72 mg/dscm into the
atmosphere from any new or
reconstructed electric arc furnace when
producing silicomanganese.
(iv) You must not discharge exhaust
gases from each electric arc furnace
operation containing polycyclic
aromatic hydrocarbon emissions in
excess of 130 mg/dscm into the
atmosphere from any existing electric
arc furnace when producing
silicomanganese.
(4) Hydrochloric acid emissions. (i)
You must not discharge exhaust gases
from each electric arc furnace operation
containing hydrochloric acid emissions
in excess of 180 mg/dscm into the
atmosphere from any new or
reconstructed electric arc furnace.
(ii) You must not discharge exhaust
gases from each electric arc furnace
operation containing hydrochloric acid
emissions in excess of 1,100 mg/dscm
into the atmosphere from any existing
electric arc furnace.
(5) Formaldehyde emissions. You
must not discharge exhaust gases from
each electric arc furnace operation
containing formaldehyde emissions in
excess of 201 mg/dscm into the
atmosphere from any new,
reconstructed or existing electric arc
furnace.
(b) Process fugitive emissions. (1) You
must install, operate and maintain a
capture system that is designed to
collect 95 percent or more of the
emissions from process fugitive
emissions sources and convey the
collected emissions to a control device
that is demonstrated to meet the
applicable emission limit specified in
paragraph (a)(1) or (c) of this section.
(2) The determination of the overall
capture must be demonstrated as
required by § 63.1624(a).
(3) Unless you meet the criteria of
paragragh (b)(3)(iii) of this section, you
must not cause the emissions exiting
from a shop building to exceed an
average of 8 percent opacity over a
furnace or MOR process cycle.
(i) This 8 percent opacity requirement
is determined by averaging the
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individual opacity readings observed
during the furnace or MOR process
cycle.
(ii) An individual opacity reading
shall be determined as the average of 24
consecutive images recorded at 15second intervals with the opacity values
from each individual digital image
rounded to the nearest 5 percent.
(iii) If the average opacity from the
shop building is greater than 8 percent
opacity during an observed furnace or
MOR process cycle, the opacity of two
more additional furnace or MOR process
cycles must be observed within 7 days
and the average of the individual
opacity readings during the three
observation periods must be less than 8
percent opacity.
(iv) At no time during operation may
the average of any two consecutive
individual opacity readings be greater
than 20 percent opacity.
(c) Local ventilation emissions. If you
operate local ventilation to capture
tapping, casting, or ladle treatment
emissions and direct them to a control
device other than one associated with
the electric arc furnace, you must not
discharge into the atmosphere any
captured emissions containing
particulate matter in excess of 4.0 mg/
dscm.
(d) MOR process. You must not
discharge into the atmosphere from any
new, reconstructed or existing MOR
process exhaust gases containing
particulate matter in excess of 3.9 mg/
dscm.
(e) Crushing and screening
equipment. You must not discharge into
the atmosphere from any new,
reconstructed, or existing piece of
equipment associated with crushing and
screening exhaust gases containing
particulate matter in excess of 13 mg/
dscm.
(f) At all times, you must operate and
maintain any affected source, including
associated air pollution control
equipment and monitoring equipment,
in a manner consistent with safety and
good air pollution control practices for
minimizing emissions. Determination of
whether such operation and
maintenance procedures are being used
will be based on information available
to the Administrator that may include,
but is not limited to, monitoring results,
review of operation and maintenance
procedures, review of operation and
maintenance records and inspection of
the source.
§ 63.1624 What are the operational and
work practice standards for new,
reconstructed, and existing facilities?
(a) Process fugitive emissions sources.
(1) You must prepare, and at all times
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operate according to, a process fugitive
emissions ventilation plan that
documents the equipment and
operations designed to effectively
capture process fugitive emissions. The
plan will be deemed to achieve effective
capture if it consists of the following
elements:
(i) Documentation of engineered
hoods and secondary fugitive capture
systems designed according to the most
recent, at the time of construction,
ventilation design principles
recommended by the American
Conference of Governmental Industrial
Hygienists (ACGIH). The process
fugitive emissions capture systems must
be designed to achieve sufficient air
changes to evacuate the collection area
frequently enough to ensure process
fugitive emissions are effectively
collected by the ventilation system and
ducted to the control device(s). The
required ventilation systems should also
use properly positioned hooding to take
advantage of the inherent air flows of
the source and capture systems that
minimize air flows while also
intercepting natural air flows or creating
air flows to contain the fugitive
emissions. Include a schematic for each
building indicating duct sizes and
locations, hood sizes and locations,
control device types, size and locations
and exhaust locations. The design plan
must identify the key operating
parameters and measurement locations
to ensure proper operation of the system
and establish monitoring parameter
values that reflect effective capture.
(ii) List of critical maintenance
actions and the schedule to conduct
them.
(2) You must submit a copy of the
process fugitive emissions ventilation
plan to the designated permitting
authority on or before the applicable
compliance date for the affected source
as specified in § 63.1621 in electronic
format and whenever an update is made
to the plan. The requirement for you to
operate the facility according to the
written process fugitives ventilation
plan and specifications must be
incorporated in the operating permit for
the facility that is issued by the
designated permitting authority under
part 70 or 71 of this chapter, as
applicable.
(3) You must update the information
required in paragraphs (a)(1) and (2) of
this section every 5 years or whenever
there is a significant change in variables
that affect process fugitives ventilation
design such as the addition of a new
process.
(b) Outdoor fugitive dust sources. (1)
You must prepare, and at all times
operate according to, an outdoor fugitive
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dust control plan that describes in detail
the measures that will be put in place
to control outdoor fugitive dust
emissions from the individual fugitive
dust sources at the facility.
(2) You must submit a copy of the
outdoor fugitive dust control plan to the
designated permitting authority on or
before the applicable compliance date
for the affected source as specified in
§ 63.1621. The requirement for you to
operate the facility according to a
written outdoor fugitive dust control
plan must be incorporated in the
operating permit for the facility that is
issued by the designated permitting
authority under part 70 or 71 of this
chapter, as applicable.
(3) You may use existing manuals that
describe the measures in place to
control outdoor fugitive dust sources
required as part of a state
implementation plan or other federally
enforceable requirement for particulate
matter to satisfy the requirements of
paragraph (b)(1) of this section.
§ 63.1625 What are the performance test
and compliance requirements for new,
reconstructed, and existing facilities?
(a) Performance testing. (1) All
performance tests must be conducted
according to the requirements in § 63.7.
(2) Each performance test in
paragraphs (c)(1) and (2) of this section
must consist of three separate and
complete runs using the applicable test
methods.
(3) Each run must be conducted under
conditions that are representative of
normal process operations.
(4) Performance tests conducted on air
pollution control devices serving
electric arc furnaces must be conducted
such that at least one tapping period, or
at least 20 minutes of a tapping period,
whichever is less, is included in at least
two of the three runs. The sampling
time for each run must be at least three
times the average tapping period of the
tested furnace, but no less than 60
minutes.
(5) You must conduct the
performance tests specified in paragraph
(c) of this section under such conditions
as the Administrator specifies based on
representative performance of the
affected source for the period being
tested. Upon request, you must make
available to the Administrator such
records as may be necessary to
determine the conditions of
performance tests.
(b) Test methods. The following test
methods in appendices of part 60 or 63
of this chapter or as specified elsewhere
must be used to determine compliance
with the emission standards.
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(1) Method 1 of appendix A–1 of 40
CFR part 60 to select the sampling port
location and the number of traverse
points.
(2) Method 2 of appendix A–1 of 40
CFR part 60 to determine the volumetric
flow rate of the stack gas.
(3)(i) Method 3A or 3B of appendix
A–2 of 40 CFR part 60 (with integrated
bag sampling) to determine the outlet
stack and inlet oxygen and CO2 content.
(ii) You must measure CO2
concentrations at both the inlet and
outlet of the positive pressure fabric
filter in conjunction with the pollutant
sampling in order to determine
isokinetic sampling rates.
(iii) As an alternative to EPA
Reference Method 3B, ASME PTC–19–
10–1981–Part 10 may be used
(incorporated by reference, see § 63.14).
(4) Method 4 of appendix A–3 of 40
CFR part 60 to determine the moisture
content of the stack gas.
(5)(i) Method 5 of appendix A–3 of 40
CFR part 60 to determine the particulate
matter concentration of the stack gas for
negative pressure baghouses and
positive pressure baghouses with stacks.
(ii) Method 5D of appendix A–3 of 40
CFR part 60 to determine particulate
matter concentration and volumetric
flow rate of the stack gas for positive
pressure baghouses without stacks.
(iii) The sample volume for each run
must be a minimum of 4.0 cubic meters
(141.2 cubic feet). For Method 5 testing
only, you may choose to collect less
than 4.0 cubic meters per run provided
that the filterable mass collected (i.e.,
net filter mass plus mass of nozzle,
probe and filter holder rinses) is equal
to or greater than 10 mg. If the total
mass collected for two of three of the
runs is less than 10 mg, you must
conduct at least one additional test run
that produces at least 10 mg of filterable
mass collected (i.e., at a greater sample
volume). Report the results of all test
runs.
(6) Method 30B of appendix A–8 of 40
CFR part 60 to measure mercury. Apply
the minimum sample volume
determination procedures as per the
method.
(7)(i) Method 26A of appendix A–8 of
40 CFR part 60 to determine outlet stack
or inlet hydrochloric acid concentration.
(ii) Collect a minimum volume of 2
cubic meters.
(8)(i) Method 316 of appendix A of
this part to determine outlet stack or
inlet formaldehyde.
(ii) Collect a minimum volume of 1.0
cubic meter.
(9) ASTM D7520–13 to determine
opacity (incorporated by reference, see
§ 63.14) with the following conditions:
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(i) During the digital camera opacity
technique (DCOT) certification
procedure outlined in Section 9.2 of
ASTM D7520–13, you or the DCOT
vendor must present the plumes in front
of various backgrounds of color and
contrast representing conditions
anticipated during field use such as blue
sky, trees and mixed backgrounds
(clouds and/or a sparse tree stand).
(ii) You must have standard operating
procedures in place including daily or
other frequency quality checks to ensure
the equipment is within manufacturing
specifications as outlined in Section 8.1
of ASTM D7520–13.
(iii) You must follow the
recordkeeping procedures outlined in
§ 63.10(b)(1) for the DCOT certification,
compliance report, data sheets and all
raw unaltered JPEGs used for opacity
and certification determination.
(iv) You or the DCOT vendor must
have a minimum of four (4)
independent technology users apply the
software to determine the visible
opacity of the 300 certification plumes.
For each set of 25 plumes, the user may
not exceed 20 percent opacity for any
one reading and the average error must
not exceed 7.5 percent opacity.
(v) Use of this method does not
provide or imply a certification or
validation of any vendor’s hardware or
software. The onus to maintain and
verify the certification and/or training of
the DCOT camera, software and operator
in accordance with ASTM D7520–13
and these requirements is on the
facility, DCOT operator and DCOT
vendor.
(10) California Air Resources Board
(CARB) Method 429 (incorporated by
reference, see § 63.14).
(11) The owner or operator may use
alternative measurement methods
approved by the Administrator
following the procedures described in
§ 63.7(f).
(c) Compliance demonstration with
the emission standards—(1) Initial
performance test. You must conduct an
initial performance test for air pollution
control devices or vent stacks subject to
§ 63.1623(a), (b)(1), and (c) through (e)
to demonstrate compliance with the
applicable emission standards.
(2) Periodic performance test. (i) You
must conduct annual particulate matter
tests for wet scrubber air pollution
control devices subject to § 63.1623(a)(1)
to demonstrate compliance with the
applicable emission standards.
(ii) You must conduct particulate
matter tests every 5 years for fabric filter
air pollution control devices subject to
§ 63.1623(a)(1) to demonstrate
compliance with the applicable
emission standards.
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(iii) You must conduct annual
mercury performance tests for wet
scrubber and fabric filter air pollution
control devices or vent stacks subject to
§ 63.1623(a)(2) to demonstrate
compliance with the applicable
emission standards.
(iv) You must conduct PAH
performance tests for wet scrubber and
fabric filter air pollution control devices
or vent stacks subject to § 63.1623(a)(3)
to demonstrate compliance with the
applicable emission standards.
(A) For furnaces producing
silicomanganese, you must conduct a
PAH performance test every 5 years for
each furnace that produces
silicomanganese subject to
§ 63.1623(a)(3).
(B) For furnaces producing
ferromanganese, you must conduct a
PAH performance test every 3 months or
2,190 cumulative hours of
ferromanganese production for each
furnace subject to § 63.1623(a)(3).
(C) If a furnace producing
ferromanganese demonstrates
compliance with four consecutive PAH
tests, the owner/operator may petition
the permitting authority to request
reduced frequency of testing to
demonstrate compliance with the PAH
emission standards. However, this PAH
compliance testing cannot be reduced to
less than once per year.
(v) You must conduct ongoing
performance tests every 5 years for air
pollution control devices or vent stacks
subject to § 63.1623(a)(4), (a)(5), (b)(1),
and (c) through (e) to demonstrate
compliance with the applicable
emission standards.
(3) Compliance is demonstrated for all
sources performing emissions tests if the
average concentration for the three runs
comprising the performance test does
not exceed the standard.
(4) Operating limits. You must
establish parameter operating limits
according to paragraphs (c)(4)(i) through
(iv) of this section. Unless otherwise
specified, compliance with each
established operating limit shall be
demonstrated for each 24-hour
operating day.
(i) For a wet particulate matter
scrubber, you must establish the
minimum liquid flow rate and pressure
drop as your operating limits during the
three-run performance test. If you use a
wet particulate matter scrubber and you
conduct separate performance tests for
particulate matter, you must establish
one set of minimum liquid flow rate and
pressure drop operating limits. If you
conduct multiple performance tests, you
must set the minimum liquid flow rate
and pressure drop operating limits at
the highest minimum hourly average
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values established during the
performance tests.
(ii) For a wet acid gas scrubber, you
must establish the minimum liquid flow
rate and pH, as your operating limits
during the three-run performance test. If
you use a wet acid gas scrubber and you
conduct separate performance tests for
hydrochloric acid, you must establish
one set of minimum liquid flow rate and
pH operating limits. If you conduct
multiple performance tests, you must
set the minimum liquid flow rate and
pH operating limits at the highest
minimum hourly average values
established during the performance
tests.
(iii) For emission sources with fabric
filters that choose to demonstrate
continuous compliance through bag leak
detection systems you must install a bag
leak detection system according to the
requirements in § 63.1626(d) and you
must set your operating limit such that
the sum duration of bag leak detection
system alarms does not exceed 5 percent
of the process operating time during a
6-month period.
(iv) If you choose to demonstrate
continuous compliance through a
particulate matter CEMS, you must
determine an operating limit
(particulate matter concentration in mg/
dscm) during performance testing for
initial particulate matter compliance.
The operating limit will be the average
of the PM filterable results of the three
Method 5 or Method 5D of appendix A–
3 of 40 CFR part 60 performance test
runs. To determine continuous
compliance, the hourly average PM
concentrations will be averaged on a
rolling 30 operating day basis. Each 30
operating day average will have to meet
the PM operating limit.
(d) Compliance demonstration with
shop building opacity standards. (1)(i) If
you are subject to § 63.1623(b), you
must conduct opacity observations of
the shop building to demonstrate
compliance with the applicable opacity
standards according to § 63.6(h)(5),
which addresses conducting opacity or
visible emission observations.
(ii) You must conduct the opacity
observations according to ASTM
D7520–13 (incorporated by reference,
see § 63.14), for a period that includes
at least one complete furnace process
cycle for each furnace.
(iii) For a shop building that contains
more than one furnace, you must
conduct the opacity observations
according to ASTM D7520–13, for a
period that includes one tapping period
from each furnace located in the shop
building.
(iv) You must conduct the opacity
observations according to ASTM
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D7520–13, for a one hour period that
includes at least one pouring for each
MOR located in the shop building.
(v) You must conduct the opacity
observations at least once per week for
each shop building containing one or
more furnaces or MOR.
(vi) You may reduce the frequency of
observations to once per month for each
shop building that demonstrates
compliance with the weekly 8-percent
opacity limit for 26 consecutive
complete observations that span a
period of at least 26 weeks. Any
monthly observation in excess of 8percent opacity will return that shop
building opacity observation to a weekly
compliance schedule. You may reduce
the frequency of observations again to
once per month for each shop building
that demonstrates compliance with the
weekly 8-percent opacity limit after
another 26 consecutive complete
observations that span a period of at
least 26 weeks.
(2) You must determine shop building
opacity operating parameters based on
either monitoring data collected during
the compliance demonstration or
established in an engineering
assessment.
(i) If you choose to establish
parameters based on the initial
compliance demonstration, you must
simultaneously monitor parameter
values for one of the following: The
capture system fan motor amperes and
all capture system damper positions, the
total volumetric flow rate to the air
pollution control device and all capture
system damper positions, or volumetric
flow rate through each separately
ducted hood that comprises the capture
system. Subsequently you must monitor
these parameters according to
§ 63.1626(g) and ensure they remain
within 10 percent of the value recorded
during the compliant opacity readings.
(ii) If you choose to establish
parameters based on an engineering
assessment, then a design analysis shall
include, for example, specifications,
drawings, schematics and ventilation
system diagrams prepared by the owner
or operator or capture or control system
manufacturer or vendor that describes
the shop building opacity system
ventilation design based on acceptable
engineering texts. The design analysis
shall address vent stream characteristics
and ventilation system design operating
parameters such as fan amps, damper
position, flow rate and/or other
specified parameters.
(iii) You may petition the
Administrator to reestablish these
parameter ranges whenever you can
demonstrate to the Administrator’s
satisfaction that the electric arc furnace
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or MOR operating conditions upon
which the parameter ranges were
previously established are no longer
applicable. The values of these
parameter ranges determined during the
most recent demonstration of
compliance must be maintained at the
appropriate level for each applicable
period.
(3) You will demonstrate continuing
compliance with the opacity standards
by following the monitoring
requirements specified in § 63.1626(g)
and the reporting and recordkeeping
requirements specified in
§ 63.1628(b)(5).
(e) Compliance demonstration with
the operational and work practice
standards—(1) Process fugitive
emissions sources. You will
demonstrate compliance by developing
and maintaining a process fugitives
ventilation plan, by reporting any
deviations from the plan and by taking
necessary corrective actions to correct
deviations or deficiencies.
(2) Outdoor fugitive dust sources. You
will demonstrate compliance by
developing and maintaining an outdoor
fugitive dust control plan, by reporting
any deviations from the plan and by
taking necessary corrective actions to
correct deviations or deficiencies.
(3) Baghouses equipped with bag leak
detection systems. You will demonstrate
compliance with the bag leak detection
system requirements by developing an
analysis and supporting documentation
demonstrating conformance with EPA
guidance and specifications for bag leak
detection systems in § 60.57c(h) of this
chapter.
§ 63.1626 What monitoring requirements
must I meet?
(a) Baghouse monitoring. You must
prepare, and at all times operate
according to, a standard operating
procedures manual that describes in
detail procedures for inspection,
maintenance and bag leak detection and
corrective action plans for all baghouses
(fabric filters or cartridge filters) that are
used to control process vents, process
fugitive, or outdoor fugitive dust
emissions from any source subject to the
emissions standards in § 63.1623.
(b) You must submit the standard
operating procedures manual for
baghouses required by paragraph (a) of
this section to the Administrator or
delegated authority for review and
approval.
(c) Unless the baghouse is equipped
with a bag leak detection system or
CEMS, the procedures that you specify
in the standard operating procedures
manual for inspections and routine
maintenance must, at a minimum,
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include the requirements of paragraphs
(c)(1) and (2) of this section.
(1) You must observe the baghouse
outlet on a daily basis for the presence
of any visible emissions.
(2) In addition to the daily visible
emissions observation, you must
conduct the following activities:
(i) Weekly confirmation that dust is
being removed from hoppers through
visual inspection, or equivalent means
of ensuring the proper functioning of
removal mechanisms.
(ii) Daily check of compressed air
supply for pulse-jet baghouses.
(iii) An appropriate methodology for
monitoring cleaning cycles to ensure
proper operation.
(iv) Monthly check of bag cleaning
mechanisms for proper functioning
through visual inspection or equivalent
means.
(v) Quarterly visual check of bag
tension on reverse air and shaker-type
baghouses to ensure that the bags are
not kinked (kneed or bent) or lying on
their sides. Such checks are not required
for shaker-type baghouses using selftensioning (spring loaded) devices.
(vi) Quarterly confirmation of the
physical integrity of the baghouse
structure through visual inspection of
the baghouse interior for air leaks.
(vii) Semiannual inspection of fans for
wear, material buildup and corrosion
through visual inspection, vibration
detectors, or equivalent means.
(d) Bag leak detection system. (1) For
each baghouse used to control emissions
from an electric arc furnace, you must
install, operate and maintain a bag leak
detection system according to
paragraphs (d)(2) through (4) of this
section, unless a system meeting the
requirements of paragraph (o) of this
section, for a CEMS and continuous
emissions rate monitoring system, is
installed for monitoring the
concentration of particulate matter. You
may choose to install, operate and
maintain a bag leak detection system for
any other baghouse in operation at the
facility according to paragraphs (d)(2)
through (4) of this section.
(2) The procedures you specified in
the standard operating procedures
manual for baghouse maintenance must
include, at a minimum, a preventative
maintenance schedule that is consistent
with the baghouse manufacturer’s
instructions for routine and long-term
maintenance.
(3) Each bag leak detection system
must meet the specifications and
requirements in paragraphs (d)(3)(i)
through (viii) of this section.
(i) The bag leak detection system must
be certified by the manufacturer to be
capable of detecting PM emissions at
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concentrations of 1.0 milligram per dry
standard cubic meter (0.00044 grains
per actual cubic foot) or less.
(ii) The bag leak detection system
sensor must provide output of relative
PM loadings.
(iii) The bag leak detection system
must be equipped with an alarm system
that will alarm when an increase in
relative particulate loadings is detected
over a preset level.
(iv) You must install and operate the
bag leak detection system in a manner
consistent with the guidance provided
in ‘‘Office of Air Quality Planning and
Standards (OAQPS) Fabric Filter Bag
Leak Detection Guidance’’ EPA–454/R–
98–015, September 1997 (incorporated
by reference, see § 63.14) and the
manufacturer’s written specifications
and recommendations for installation,
operation and adjustment of the system.
(v) The initial adjustment of the
system must, at a minimum, consist of
establishing the baseline output by
adjusting the sensitivity (range) and the
averaging period of the device and
establishing the alarm set points and the
alarm delay time.
(vi) Following initial adjustment, you
must not adjust the sensitivity or range,
averaging period, alarm set points, or
alarm delay time, except as detailed in
the approved standard operating
procedures manual required under
paragraph (a) of this section. You cannot
increase the sensitivity by more than
100 percent or decrease the sensitivity
by more than 50 percent over a 365-day
period unless such adjustment follows a
complete baghouse inspection that
demonstrates that the baghouse is in
good operating condition.
(vii) You must install the bag leak
detector downstream of the baghouse.
(viii) Where multiple detectors are
required, the system’s instrumentation
and alarm may be shared among
detectors.
(4) You must include in the standard
operating procedures manual required
by paragraph (a) of this section a
corrective action plan that specifies the
procedures to be followed in the case of
a bag leak detection system alarm. The
corrective action plan must include, at
a minimum, the procedures that you
will use to determine and record the
time and cause of the alarm as well as
the corrective actions taken to minimize
emissions as specified in paragraphs
(d)(4)(i) and (ii) of this section.
(i) The procedures used to determine
the cause of the alarm must be initiated
within 30 minutes of the alarm.
(ii) The cause of the alarm must be
alleviated by taking the necessary
corrective action(s) that may include,
but not be limited to, those listed in
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paragraphs (d)(4)(ii)(A) through (F) of
this section.
(A) Inspecting the baghouse for air
leaks, torn or broken filter elements, or
any other malfunction that may cause
an increase in emissions.
(B) Sealing off defective bags or filter
media.
(C) Replacing defective bags or filter
media, or otherwise repairing the
control device.
(D) Sealing off a defective baghouse
compartment.
(E) Cleaning the bag leak detection
system probe, or otherwise repairing the
bag leak detection system.
(F) Shutting down the process
producing the particulate emissions.
(e) If you use a wet particulate matter
scrubber, you must collect the pressure
drop and liquid flow rate monitoring
system data according to § 63.1628,
reduce the data to 24-hour block
averages and maintain the 24-hour
average pressure drop and liquid flowrate at or above the operating limits
established during the performance test
according to § 63.1625(c)(4)(i).
(f) If you use curtains or partitions to
prevent process fugitive emissions from
escaping the area around the process
fugitive emission source or other parts
of the building, you must perform
quarterly inspections of the physical
condition of these curtains or partitions
to determine if there are any tears or
openings.
(g) Shop building opacity. In order to
demonstrate continuous compliance
with the opacity standards in § 63.1623,
you must comply with the requirements
§ 63.1625(d)(1) and one of the
monitoring options in paragraphs (g)(1)
or (2) of this section. The selected
option must be consistent with that
selected during the initial performance
test described in § 63.1625(d)(2).
Alternatively, you may use the
provisions of § 63.8(f) to request
approval to use an alternative
monitoring method.
(1) If you choose to establish
operating parameters during the
compliance test as specified in
§ 63.1625(d)(2)(i), you must meet one of
the following requirements.
(i) Check and record the control
system fan motor amperes and capture
system damper positions once per shift.
(ii) Install, calibrate and maintain a
monitoring device that continuously
records the volumetric flow rate through
each separately ducted hood.
(iii) Install, calibrate and maintain a
monitoring device that continuously
records the volumetric flow rate at the
inlet of the air pollution control device
and check and record the capture
system damper positions once per shift.
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(2) If you choose to establish
operating parameters during the
compliance test as specified in
§ 63.1625(d)(2)(ii), you must monitor the
selected parameter(s) on a frequency
specified in the assessment and
according to a method specified in the
engineering assessment
(3) All flow rate monitoring devices
must meet the following requirements:
(i) Be installed in an appropriate
location in the exhaust duct such that
reproducible flow rate monitoring will
result.
(ii) Have an accuracy ±10 percent over
its normal operating range and be
calibrated according to the
manufacturer’s instructions.
(4) The Administrator may require
you to demonstrate the accuracy of the
monitoring device(s) relative to Methods
1 and 2 of appendix A–1 of part 60 of
this chapter.
(5) Failure to maintain the appropriate
capture system parameters (e.g., fan
motor amperes, flow rate and/or damper
positions) establishes the need to
initiate corrective action as soon as
practicable after the monitoring
excursion in order to minimize excess
emissions.
(h) Furnace capture system. You must
perform quarterly (once every three
months) inspections of the furnace
fugitive capture system equipment to
ensure that the hood locations have not
been changed or obstructed because of
contact with cranes or ladles, quarterly
inspections of the physical condition of
hoods and ductwork to the control
device to determine if there are any
openings or leaks in the ductwork,
quarterly inspections of the hoods and
ductwork to determine if there are any
flow constrictions in ductwork due to
dents or accumulated dust and quarterly
examinations of the operational status of
flow rate controllers (pressure sensors,
dampers, damper switches, etc.) to
ensure they are operating correctly. Any
deficiencies must be recorded and
proper maintenance and repairs
performed.
(i) Requirements for sources using
CMS. If you demonstrate compliance
with any applicable emissions limit
through use of a continuous monitoring
system (CMS), where a CMS includes a
continuous parameter monitoring
system (CPMS) as well as a continuous
emissions monitoring system (CEMS),
you must develop a site-specific
monitoring plan and submit this sitespecific monitoring plan, if requested, at
least 60 days before your initial
performance evaluation (where
applicable) of your CMS. Your sitespecific monitoring plan must address
the monitoring system design, data
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collection and the quality assurance and
quality control elements outlined in this
paragraph and in § 63.8(d). You must
install, operate and maintain each CMS
according to the procedures in your
approved site-specific monitoring plan.
Using the process described in
§ 63.8(f)(4), you may request approval of
monitoring system quality assurance
and quality control procedures
alternative to those specified in
paragraphs (i)(1) through (6) of this
section in your site-specific monitoring
plan.
(1) The performance criteria and
design specifications for the monitoring
system equipment, including the sample
interface, detector signal analyzer and
data acquisition and calculations;
(2) Sampling interface location such
that the monitoring system will provide
representative measurements;
(3) Equipment performance checks,
system accuracy audits, or other audit
procedures;
(4) Ongoing operation and
maintenance procedures in accordance
with the general requirements of
§ 63.8(c)(1) and (3);
(5) Conditions that define a
continuous monitoring system that is
out of control consistent with
§ 63.8(c)(7)(i) and for responding to out
of control periods consistent with
§ 63.8(c)(7)(ii) and (c)(8) or Table 1 to
this subpart, as applicable; and
(6) Ongoing recordkeeping and
reporting procedures in accordance with
provisions in § 63.10(c), (e)(1) and
(e)(2)(i), and Table 1 to this subpart, as
applicable.
(j) If you have an operating limit that
requires the use of a CPMS, you must
install, operate and maintain each
continuous parameter monitoring
system according to the procedures in
paragraphs (j)(1) through (7) of this
section.
(1) The CPMS must complete a
minimum of one cycle of operation for
each successive 15-minute period. You
must have a minimum of four
successive cycles of operation to have a
valid hour of data.
(2) Except for periods of monitoring
system malfunctions, repairs associated
with monitoring system malfunctions
and required monitoring system quality
assurance or quality control activities
(including, as applicable, system
accuracy audits and required zero and
span adjustments), you must operate the
CMS at all times the affected source is
operating. A monitoring system
malfunction is any sudden, infrequent,
not reasonably preventable failure of the
monitoring system to provide valid data.
Monitoring system failures that are
caused in part by poor maintenance or
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careless operation are not malfunctions.
You are required to complete
monitoring system repairs in response
to monitoring system malfunctions and
to return the monitoring system to
operation as expeditiously as
practicable.
(3) You may not use data recorded
during monitoring system malfunctions,
repairs associated with monitoring
system malfunctions, or required
monitoring system quality assurance or
control activities in calculations used to
report emissions or operating levels.
You must use all the data collected
during all other required data collection
periods in assessing the operation of the
control device and associated control
system.
(4) Except for periods of monitoring
system malfunctions, repairs associated
with monitoring system malfunctions
and required quality monitoring system
quality assurance or quality control
activities (including, as applicable,
system accuracy audits and required
zero and span adjustments), failure to
collect required data is a deviation of
the monitoring requirements.
(5) You must conduct other CPMS
equipment performance checks, system
accuracy audits, or other audit
procedures specified in your sitespecific monitoring plan at least once
every 12 months.
(6) You must conduct a performance
evaluation of each CPMS in accordance
with your site-specific monitoring plan.
(7) You must record the results of
each inspection, calibration and
validation check.
(k) CPMS for measuring gaseous flow.
(1) Use a flow sensor with a
measurement sensitivity of 5 percent of
the flow rate or 10 cubic feet per
minute, whichever is greater;
(2) Check all mechanical connections
for leakage at least every month; and
(3) Perform a visual inspection at least
every 3 months of all components of the
flow CPMS for physical and operational
integrity and all electrical connections
for oxidation and galvanic corrosion if
your flow CPMS is not equipped with
a redundant flow sensor.
(l) CPMS for measuring liquid flow.
(1) Use a flow sensor with a
measurement sensitivity of 2 percent of
the liquid flow rate; and
(2) Reduce swirling flow or abnormal
velocity distributions due to upstream
and downstream disturbances.
(m) CPMS for measuring pressure. (1)
Minimize or eliminate pulsating
pressure, vibration and internal and
external corrosion; and
(2) Use a gauge with a minimum
tolerance of 1.27 centimeters of water or
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a transducer with a minimum tolerance
of 1 percent of the pressure range.
(3) Perform checks at least once each
process operating day to ensure pressure
measurements are not obstructed (e.g.,
check for pressure tap pluggage daily).
(n) CPMS for measuring pH. (1)
Ensure the sample is properly mixed
and representative of the fluid to be
measured.
(2) Check the pH meter’s calibration
on at least two points every eight hours
of process operation.
(o) Particulate Matter CEMS. If you
are using a CEMS to measure particulate
matter emissions to meet requirements
of this subpart, you must install, certify,
operate and maintain the particulate
matter CEMS as specified in paragraphs
(o)(1) through (4) of this section.
(1) You must conduct a performance
evaluation of the PM CEMS according to
the applicable requirements of § 60.13 of
this chapter and Performance
Specification 11 at 40 CFR part 60,
appendix B.
(2) During each PM correlation testing
run of the CEMS required by
Performance Specification 11 at 40 CFR
part 60, appendix B, PM and oxygen (or
carbon dioxide) collect data
concurrently (or within a 30- to 60minute period) by both the CEMS and
by conducting performance tests using
Method 5 or 5D at 40 CFR part 60,
appendix A–3 or Method 17 at 40 CFR
part 60, appendix A–6.
(3) Perform quarterly accuracy
determinations and daily calibration
drift tests in accordance with Procedure
2 at 40 CFR part 60, appendix F.
Relative Response Audits must be
performed annually and Response
Correlation Audits must be performed
every 3 years.
(4) Within 60 days after the date of
completing each CEMS relative
accuracy test audit or performance test
conducted to demonstrate compliance
with this subpart, you must submit the
relative accuracy test audit data and the
results of the performance test as
specified in § 63.1628(e).
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§ 63.1627 What notification requirements
must I meet?
(a) You must comply with all of the
notification requirements of § 63.9.
Electronic notifications are encouraged
when possible.
(b)(1) You must submit the process
fugitive ventilation plan required under
§ 63.1624(a), the outdoor fugitive dust
control plan required under
§ 63.1624(b), the site-specific
monitoring plan for CMS required under
§ 63.1626(i) and the standard operating
procedures manual for baghouses
required under § 63.1626(a) to the
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Administrator or delegated authority.
You must submit this notification no
later than June 30, 2016. For sources
that commenced construction or
reconstruction after June 30, 2015, you
must submit this notification no later
than 180 days before startup of the
constructed or reconstructed
ferromanganese or silicomanganese
production facility. For an affected
source that has received a construction
permit from the Administrator or
delegated authority on or before June 30,
2015, you must submit this notification
no later than June 30, 2016.
(2) The plans and procedures
documents submitted as required under
paragraph (b)(1) of this section must be
submitted to the Administrator in
electronic format and whenever an
update is made to the procedure.
§ 63.1628 What recordkeeping and
reporting requirements must I meet?
(a) You must comply with all of the
recordkeeping and reporting
requirements specified in § 63.10 of the
General Provisions that are referenced
in Table 1 to this subpart.
(1) Records must be maintained in a
form suitable and readily available for
expeditious review, according to
§ 63.10(b)(1). However, electronic
recordkeeping and reporting is
encouraged and required for some
records and reports.
(2) Records must be kept on site for
at least 2 years after the date of
occurrence, measurement, maintenance,
corrective action, report, or record,
according to § 63.10(b)(1).
(b) You must maintain, for a period of
5 years, records of the information listed
in paragraphs (b)(1) through (11) of this
section.
(1) Electronic records of the bag leak
detection system output.
(2) An identification of the date and
time of all bag leak detection system
alarms, the time that procedures to
determine the cause of the alarm were
initiated, the cause of the alarm, an
explanation of the corrective actions
taken and the date and time the cause
of the alarm was corrected.
(3) All records of inspections and
maintenance activities required under
§ 63.1626(c) as part of the practices
described in the standard operating
procedures manual for baghouses
required under § 63.1626(a).
(4) Electronic records of the pressure
drop and water flow rate values for wet
scrubbers used to control particulate
matter emissions as required in
§ 63.1626(e), identification of periods
when the 1-hour average pressure drop
and water flow rate values are below the
established minimum operating limits
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and an explanation of the corrective
actions taken.
(5) Electronic records of the shop
building capture system monitoring
required under § 63.1626(g)(1) and (2),
as applicable, or identification of
periods when the capture system
parameters were not maintained and an
explanation of the corrective actions
taken.
(6) Records of the results of quarterly
inspections of the furnace capture
system required under § 63.1626(h).
(7) Electronic records of the
continuous flow monitors or pressure
monitors required under § 63.1626(i)
and (j) and an identification of periods
when the flow rate or pressure was not
maintained as required in § 63.1626(e).
(8) Electronic records of the output of
any CEMS installed to monitor
particulate matter emissions meeting the
requirements of § 63.1626(i).
(9) Records of the occurrence and
duration of each startup and/or
shutdown.
(10) Records of the occurrence and
duration of each malfunction of
operation (i.e., process equipment) or
the air pollution control equipment and
monitoring equipment.
(11) Records that explain the periods
when the procedures outlined in the
process fugitives ventilation plan
required under § 63.1624(a), the
fugitives dust control plan required
under § 63.1624(b), the site-specific
monitoring plan for CMS required under
§ 63.1626(i) and the standard operating
procedures manual for baghouses
required under § 63.1626(a).
(c) You must comply with all of the
reporting requirements specified in
§ 63.10 of the General Provisions that
are referenced in Table 1 to this subpart.
(1) You must submit reports no less
frequently than specified under
§ 63.10(e)(3) of the General Provisions.
(2) Once a source reports a violation
of the standard or excess emissions, you
must follow the reporting format
required under § 63.10(e)(3) until a
request to reduce reporting frequency is
approved by the Administrator.
(d) In addition to the information
required under the applicable sections
of § 63.10, you must include in the
reports required under paragraph (c) of
this section the information specified in
paragraphs (d)(1) through (7) of this
section.
(1) Reports that identify and explain
the periods when the procedures
outlined in the process fugitives
ventilation plan required under
§ 63.1624(a), the fugitives dust control
plan required under § 63.1624(b), the
site-specific monitoring plan for CMS
required under § 63.1626(i) and the
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standard operating procedures manual
for baghouses required under
§ 63.1626(a) were not followed.
(2) Reports that identify the periods
when the average hourly pressure drop
or flow rate of wet scrubbers used to
control particulate emissions dropped
below the levels established in
§ 63.1626(e) and an explanation of the
corrective actions taken.
(3) Bag leak detection system. Reports
including the following information:
(i) Records of all alarms.
(ii) Description of the actions taken
following each bag leak detection
system alarm.
(4) Reports of the shop building
capture system monitoring required
under § 63.1626(g)(1) and (2), as
applicable, identification of periods
when the capture system parameters
were not maintained and an explanation
of the corrective actions taken.
(5) Reports of the results of quarterly
inspections of the furnace capture
system required under § 63.1626(h).
(6) Reports of the CPMS required
under § 63.1626, an identification of
periods when the monitored parameters
were not maintained as required in
§ 63.1626 and corrective actions taken.
(7) If a malfunction occurred during
the reporting period, the report must
include the number, duration and a
brief description for each type of
malfunction that occurred during the
reporting period and caused or may
have caused any applicable emissions
limitation to be exceeded. The report
must also include a description of
actions taken by the owner or operator
during a malfunction of an affected
source to minimize emissions in
accordance with § 63.1623(f), including
actions taken to correct a malfunction.
(e) Within 60 days after the date of
completing each CEMS relative
accuracy test audit or performance test
conducted to demonstrate compliance
with this subpart, you must submit the
relative accuracy test audit data and the
results of the performance test in the
method specified by paragraphs (e)(1)
and (2) of this section. The results of the
performance test must contain the
information listed in paragraph (e)(2) of
this section.
(1)(i) Within 60 days after the date of
completing each performance test (as
defined in § 63.2) required by this
subpart, you must submit the results of
the performance tests, including any
associated fuel analyses, following the
procedure specified in either paragraph
(e)(1)(i)(A) or (B) of this section.
(A) For data collected using test
methods supported by the EPA’s
Electronic Reporting Tool (ERT) as
listed on the EPA’s ERT Web site
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(https://www.epa.gov/ttn/chief/ert/
index.html), you must submit the results
of the performance test to the EPA via
the Compliance and Emissions Data
Reporting Interface (CEDRI). CEDRI can
be accessed through the EPA’s Central
Data Exchange (CDX) (https://
cdx.epa.gov/epa_home.asp).
Performance test data must be submitted
in a file format generated through the
use of the EPA’s ERT. Alternatively, you
may submit performance test data in an
electronic file format consistent with the
extensible markup language (XML)
schema listed on the EPA’s ERT Web
site once the XML schema is available.
If you claim that some of the
performance test information being
submitted is confidential business
information (CBI), you must submit a
complete file generated through the use
of the EPA’s ERT or an alternate
electronic file consistent with the XML
schema listed on the EPA’s ERT Web
site, including information claimed to
be CBI, on a compact disk, flash drive,
or other commonly used electronic
storage media to the EPA. The electronic
media must be clearly marked as CBI
and mailed to U.S. EPA/OAQPS/CORE
CBI Office, Attention: Group Leader,
Measurement Policy Group, MD C404–
02, 4930 Old Page Rd., Durham, NC
27703. The same ERT or alternate file
with the CBI omitted must be submitted
to the EPA via the EPA’s CDX as
described earlier in this paragraph
(e)(1)(i)(A).
(B) For data collected using test
methods that are not supported by the
EPA’s ERT as listed on the EPA’s ERT
Web site, you must submit the results of
the performance test to the
Administrator at the appropriate
address listed in § 63.13.
(ii) Within 60 days after the date of
completing each CEMS performance
evaluation (as defined in § 63.2), you
must submit the results of the
performance evaluation following the
procedure specified in either paragraph
(b)(1) or (2) of this section.
(A) For performance evaluations of
continuous monitoring systems
measuring relative accuracy test audit
(RATA) pollutants that are supported by
the EPA’s ERT as listed on the EPA’s
ERT Web site, you must submit the
results of the performance evaluation to
the EPA via the CEDRI. (CEDRI can be
accessed through the EPA’s CDX.)
Performance evaluation data must be
submitted in a file format generated
through the use of the EPA’s ERT.
Alternatively, you may submit
performance evaluation data in an
electronic file format consistent with the
XML schema listed on the EPA’s ERT
Web site, once the XML schema is
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available. If you claim that some of the
performance evaluation information
being transmitted is CBI, you must
submit a complete file generated
through the use of the EPA’s ERT or an
alternative electronic file consistent
with the XML schema listed on the
EPA’s ERT Web site, including
information claimed to be CBI, on a
compact disk, flash drive or other
commonly used electronic storage
media to the EPA. The electronic storage
media must be clearly marked as CBI
and mailed to U.S. EPA/OAQPS/CORE
CBI Office, Attention: Group Leader,
Measurement Policy Group, MD C404–
02, 4930 Old Page Rd., Durham, NC
27703. The same ERT file or alternate
file with the CBI omitted must be
submitted to the EPA via the EPA’s CDX
as described earlier in this paragraph
(e)(1)(ii)(A).
(B) For any performance evaluations
of continuous monitoring systems
measuring RATA pollutants that are not
supported by the EPA’s ERT as listed on
the EPA’s ERT Web site, you must
submit the results of the performance
evaluation to the Administrator at the
appropriate address listed in § 63.13.
(2) The results of a performance test
shall include the purpose of the test; a
brief process description; a complete
unit description, including a description
of feed streams and control devices;
sampling site description; pollutants
measured; description of sampling and
analysis procedures and any
modifications to standard procedures;
quality assurance procedures; record of
operating conditions, including
operating parameters for which limits
are being set, during the test; record of
preparation of standards; record of
calibrations; raw data sheets for field
sampling; raw data sheets for field and
laboratory analyses; chain-of-custody
documentation; explanation of
laboratory data qualifiers; example
calculations of all applicable stack gas
parameters, emission rates, percent
reduction rates and analytical results, as
applicable; and any other information
required by the test method, a relevant
standard, or the Administrator.
§ 63.1629 Who implements and enforces
this subpart?
(a) This subpart can be implemented
and enforced by the U.S. EPA, or a
delegated authority such as the
applicable state, local, or tribal agency.
If the U.S. EPA Administrator has
delegated authority to a state, local, or
tribal agency, then that agency, in
addition to the U.S. EPA, has the
authority to implement and enforce this
subpart. Contact the applicable U.S.
EPA Regional Office to find out if this
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subpart is delegated to a state, local, or
tribal agency.
(b) In delegating implementation and
enforcement authority of this subpart to
a state, local, or tribal agency under
subpart E of this part, the authorities
contained in paragraph (c) of this
section are retained by the
Administrator of U.S. EPA and cannot
be transferred to the state, local, or tribal
agency.
(c) The authorities that cannot be
delegated to state, local, or tribal
agencies are as specified in paragraphs
(c)(1) through (4) of this section.
(1) Approval of alternatives to
requirements in §§ 63.1620 and 63.1621
and 63.1623 and 63.1624.
(2) Approval of major alternatives to
test methods under § 63.7(e)(2)(ii) and
(f), as defined in § 63.90 and as required
in this subpart.
(3) Approval of major alternatives to
monitoring under § 63.8(f), as defined in
§ 63.90 and as required in this subpart.
(4) Approval of major alternatives to
recordkeeping and reporting under
§ 63.10(f), as defined in § 63.90 and as
required in this subpart.
■ 4. Section 63.1650 is amended by:
■ a. Revising paragraph (d);
■ b. Removing and reserving paragraph
(e)(1); and
■ c. Revising paragraph (e)(2).
The revisions read as follows:
§ 63.1650
dates.
Applicability and compliance
*
*
*
*
*
(d) Table 1 to this subpart specifies
the provisions of subpart A of this part
that apply to owners and operators of
ferroalloy production facilities subject
to this subpart.
(e) * * *
(2) Each owner or operator of a new
or reconstructed affected source that
commences construction or
reconstruction after August 4, 1998 and
before November 23, 2011, must comply
with the requirements of this subpart by
May 20, 1999 or upon startup of
operations, whichever is later.
■ 5. Section 63.1652 is amended by
adding paragraph (f) to read as follows:
§ 63.1652
Emission standards.
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*
*
*
*
*
(f) At all times, you must operate and
maintain any affected source, including
associated air pollution control
equipment and monitoring equipment,
in a manner consistent with safety and
good air pollution control practices for
minimizing emissions. Determination of
whether such operation and
maintenance procedures are being used
will be based on information available
to the Administrator that may include,
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but is not limited to, monitoring results,
review of operation and maintenance
procedures, review of operation and
maintenance records and inspection of
the source.
■ 6. Section 63.1656 is amended by:
■ a. Adding paragraph (a)(6);
■ b. Revising paragraphs (b)(7) and
(e)(1); and
■ c. Removing and reserving paragraph
(e)(2)(ii).
The addition and revisions read as
follows:
§ 63.1656 Performance testing, test
methods, and compliance demonstrations.
(a) * * *
(6) You must conduct the
performance tests specified in paragraph
(c) of this section under such conditions
as the Administrator specifies based on
representative performance of the
affected source for the period being
tested. Upon request, you must make
available to the Administrator such
records as may be necessary to
determine the conditions of
performance tests.
(b) * * *
(7) Method 9 of appendix A–4 of 40
CFR part 60 to determine opacity.
ASTM D7520–13, ‘‘Standard Test
Method for Determining the Opacity of
a Plume in the Outdoor Ambient
Atmosphere’’ may be used (incorporated
by reference, see § 63.14) with the
following conditions:
(i) During the digital camera opacity
technique (DCOT) certification
procedure outlined in Section 9.2 of
ASTM D7520–13, the owner or operator
or the DCOT vendor must present the
plumes in front of various backgrounds
of color and contrast representing
conditions anticipated during field use
such as blue sky, trees and mixed
backgrounds (clouds and/or a sparse
tree stand).
(ii) The owner or operator must also
have standard operating procedures in
place including daily or other frequency
quality checks to ensure the equipment
is within manufacturing specifications
as outlined in Section 8.1 of ASTM
D7520–13.
(iii) The owner or operator must
follow the recordkeeping procedures
outlined in § 63.10(b)(1) for the DCOT
certification, compliance report, data
sheets and all raw unaltered JPEGs used
for opacity and certification
determination.
(iv) The owner or operator or the
DCOT vendor must have a minimum of
four (4) independent technology users
apply the software to determine the
visible opacity of the 300 certification
plumes. For each set of 25 plumes, the
user may not exceed 15 percent opacity
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37399
of any one reading and the average error
must not exceed 7.5 percent opacity.
(v) Use of this approved alternative
does not provide or imply a certification
or validation of any vendor’s hardware
or software. The onus to maintain and
verify the certification and/or training of
the DCOT camera, software and operator
in accordance with ASTM D7520–13
and these requirements is on the
facility, DCOT operator and DCOT
vendor.
*
*
*
*
*
(e) * * *
(1) Fugitive dust sources. Failure to
have a fugitive dust control plan or
failure to report deviations from the
plan and take necessary corrective
action would be a violation of the
general duty to ensure that fugitive dust
sources are operated and maintained in
a manner consistent with good air
pollution control practices for
minimizing emissions per § 63.1652(f).
*
*
*
*
*
■ 7. Section 63.1657 is amended by
revising paragraphs (a)(6), (b)(3), and
(c)(7) to read as follows:
§ 63.1657
Monitoring requirements.
(a) * * *
(6) Failure to monitor or failure to
take corrective action under the
requirements of paragraph (a) of this
section would be a violation of the
general duty to operate in a manner
consistent with good air pollution
control practices that minimizes
emissions per § 63.1652(f).
(b) * * *
(3) Failure to monitor or failure to
take corrective action under the
requirements of paragraph (b) of this
section would be a violation of the
general duty to operate in a manner
consistent with good air pollution
control practices that minimizes
emissions per § 63.1652(f).
(c) * * *
(7) Failure to monitor or failure to
take corrective action under the
requirements of paragraph (c) of this
section would be a violation of the
general duty to operate in a manner
consistent with good air pollution
control practices that minimizes
emissions per § 63.1652(f).
■ 8. Section 63.1659 is amended by
revising paragraph (a)(4) to read as
follows:
§ 63.1659
Reporting requirements.
(a) * * *
(4) Reporting malfunctions. If a
malfunction occurred during the
reporting period, the report must
include the number, duration and a
brief description for each type of
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malfunction which occurred during the
reporting period and which caused or
may have caused any applicable
emission limitation to be exceeded. The
report must also include a description of
actions taken by an owner or operator
during a malfunction of an affected
source to minimize emissions in
accordance with § 63.1652(f), including
actions taken to correct a malfunction.
*
*
*
*
*
■
9. Section 63.1660 is amended by:
a. Revising paragraphs (a)(2)(i) and
(ii); and
■ b. Removing and reserving paragraphs
(a)(2)(iv) and (v).
The revisions read as follows:
■
§ 63.1660
Recordkeeping requirements.
(a) * * *
(2) * * *
(i) Records of the occurrence and
duration of each malfunction of
operation (i.e., process equipment) or
the air pollution control equipment and
monitoring equipment;
(ii) Records of actions taken during
periods of malfunction to minimize
emissions in accordance with
§ 63.1652(f), including corrective
actions to restore malfunctioning
process and air pollution control and
monitoring equipment to its normal or
usual manner of operation;
*
*
*
*
*
10. Add Table 1 to the end of subpart
XXX to read as follows:
■
TABLE 1—TO SUBPART XXX OF PART 63—GENERAL PROVISIONS APPLICABILITY TO SUBPART XXX
Reference
Applies to subpart XXX
§ 63.1 ................................................................................
§ 63.2 ................................................................................
§ 63.3 ................................................................................
§ 63.4 ................................................................................
§ 63.5 ................................................................................
§ 63.6(a), (b), (c) ...............................................................
§ 63.6(d) ............................................................................
§ 63.6(e)(1)(i) ....................................................................
Yes .....................................
Yes .....................................
Yes .....................................
Yes .....................................
Yes .....................................
Yes .....................................
No .......................................
No .......................................
§ 63.6(e)(1)(ii) ....................................................................
§ 63.6(e)(1)(iii) ...................................................................
§ 63.6(e)(2) ........................................................................
§ 63.6(e)(3) ........................................................................
§ 63.6(f)(1) .........................................................................
§ 63.6(f)(2)–(3) ..................................................................
§ 63.6(g) ............................................................................
§ 63.6(h)(1) ........................................................................
§ 63.6(h)(2)–(9) .................................................................
§ 63.6(i) .............................................................................
§ 63.6(j) .............................................................................
§ 63.7(a)–(d) ......................................................................
§ 63.7(e)(1) ........................................................................
§ 63.7(e)(2)–(4) .................................................................
§ 63.7(f), (g), (h) ................................................................
§ 63.8(a)–(b) ......................................................................
§ 63.8(c)(1)(i) .....................................................................
No .......................................
Yes .....................................
No .......................................
No .......................................
No .......................................
Yes .....................................
Yes .....................................
No .......................................
Yes .....................................
Yes .....................................
Yes .....................................
Yes .....................................
No .......................................
Yes .....................................
Yes .....................................
Yes .....................................
No .......................................
§ 63.8(c)(1)(ii) ....................................................................
§ 63.8(c)(1)(iii) ...................................................................
§ 63.8(c)(2)–(d)(2) .............................................................
§ 63.8(d)(3) ........................................................................
Yes .....................................
No .......................................
Yes .....................................
Yes, except for last sentence.
Yes .....................................
Yes .....................................
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§ 63.8(e)–(g) ......................................................................
§ 63.9(a),(b),(c),(e),(g),(h)(1) through (3), (h)(5) and (6),
(i) and (j).
§ 63.9(f) .............................................................................
§ 63.9(h)(4) ........................................................................
§ 63.10(a) ..........................................................................
§ 63.10(b)(1) ......................................................................
§ 63.10(b)(2)(i) ..................................................................
§ 63.10(b)(2)(ii) ..................................................................
Yes .....................................
No .......................................
Yes .....................................
Yes .....................................
No .......................................
No .......................................
§ 63.10(b)(2)(iii) .................................................................
§ 63.10(b)(2)(iv)–(v) ..........................................................
§ 63.10(b)(2)(vi)–(xiv) ........................................................
§ 63.10)(b)(3) ....................................................................
§ 63.10(c)(1)–(9) ...............................................................
§ 63.10(c)(10)–(11) ...........................................................
Yes .....................................
No .......................................
Yes .....................................
Yes .....................................
Yes .....................................
No .......................................
§ 63.10(c)(12)–(14) ...........................................................
§ 63.10(c)(15) ....................................................................
§ 63.10(d)(1)–(4) ...............................................................
§ 63.10(d)(5) ......................................................................
Yes .....................................
No .......................................
Yes .....................................
No .......................................
§ 63.10(e)–(f) .....................................................................
Comment
Section reserved.
See §§ 63.1623(g) and 63.1652(f) for general duty requirement.
Section reserved.
See §§ 63.1625(a)(5) and 63.1656(a)(6).
See §§ 63.1623(g) and 63.1652(f) for general duty requirement.
SSM plans are not required.
Section reserved.
See §§ 63.1628 and 63.1660 for recordkeeping of (1)
occurrence and duration and (2) actions taken during
malfunction.
Yes .....................................
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See §§ 63.1628 and 63.1660 for malfunction recordkeeping requirements.
See §§ 63.1628(d)(8) and 63.1659(a)(4) for malfunction
reporting requirements.
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37401
TABLE 1—TO SUBPART XXX OF PART 63—GENERAL PROVISIONS APPLICABILITY TO SUBPART XXX—Continued
Reference
Applies to subpart XXX
Comment
§ 63.11 ..............................................................................
No .......................................
Flares will not be used to comply with the emission limits.
§§ 63.12–63.15 .................................................................
Yes .....................................
[FR Doc. 2015–15038 Filed 6–29–15; 8:45 am]
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BILLING CODE 6560–50–P
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Agencies
[Federal Register Volume 80, Number 125 (Tuesday, June 30, 2015)]
[Rules and Regulations]
[Pages 37365-37401]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-15038]
[[Page 37365]]
Vol. 80
Tuesday,
No. 125
June 30, 2015
Part II
Environmental Protection Agency
-----------------------------------------------------------------------
40 CFR Part 63
National Emissions Standards for Hazardous Air Pollutants: Ferroalloys
Production; Final Rule
Federal Register / Vol. 80 , No. 125 / Tuesday, June 30, 2015 / Rules
and Regulations
[[Page 37366]]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 63
[EPA-HQ-OAR-2010-0895; FRL-9928-66-OAR]
RIN 2060-AQ11
National Emissions Standards for Hazardous Air Pollutants:
Ferroalloys Production
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This action finalizes the residual risk and technology review
(RTR) conducted for the Ferroalloys Production source category
regulated under national emission standards for hazardous air
pollutants (NESHAP). These final amendments include revisions to
particulate matter (PM) standards for electric arc furnaces, metal
oxygen refining processes, and crushing and screening operations, and
expand and revise the requirements to control process fugitive
emissions from furnace operations, tapping, casting, and other
processes. We are also finalizing opacity limits, as proposed in 2014.
However, regarding opacity monitoring, in lieu of Method 9, we are
requiring monitoring with the digital camera opacity technique (DCOT).
Furthermore, we are finalizing emissions standards for four previously
unregulated hazardous air pollutants (HAP): Formaldehyde, hydrogen
chloride (HCl), mercury (Hg) and polycyclic aromatic hydrocarbons
(PAH). Other requirements related to testing, monitoring, notification,
recordkeeping, and reporting are included. This rule is health
protective due to the revised emissions limits for the stacks and the
requirement of enhanced fugitive emissions controls that will achieve
significant reductions of process fugitive emissions, especially
manganese.
DATES: This final action is effective on June 30, 2015. The
incorporation by reference of certain publications listed in the rule
is approved by the Director of the Federal Register as of June 30,
2015.
ADDRESSES: The Environmental Protection Agency (EPA) has established a
docket for this action under Docket ID No. EPA-HQ-OAR-2010-0895. All
documents in the docket are listed on the www.regulations.gov Web site.
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 through
https://www.regulations.gov, or in hard copy at the EPA Docket Center,
EPA WJC West Building, Room Number 3334, 1301 Constitution Ave. NW.,
Washington, DC. The Public Reading Room hours of operation are 8:30
a.m. to 4:30 p.m. Eastern Standard Time (EST), Monday through Friday.
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: For questions about this final action,
contact Phil Mulrine, Sector Policies and Programs Division (D243-02),
Office of Air Quality Planning and Standards, U.S. Environmental
Protection Agency, Research Triangle Park, North Carolina, 27711;
telephone number: (919) 541-5289; fax number: (919) 541-3207; and email
address: mulrine.phil@epa.gov. For specific information regarding the
risk modeling methodology, contact Darcie Smith, Health and
Environmental Impacts Division (C539-02), Office of Air Quality
Planning and Standards, U.S. Environmental Protection Agency, Research
Triangle Park, North Carolina 27711; telephone number: (919) 541-2076;
fax number: (919) 541-0840; and email address: smith.darcie@epa.gov.
For information about the applicability of the NESHAP to a particular
entity, contact Cary Secrest, Office of Enforcement and Compliance
Assurance, U.S. Environmental Protection Agency, EPA WJC Building, 1200
Pennsylvania Ave. NW., Washington, DC 20460; telephone number: (202)
564-8661; and email address: secrest.cary@epa.gov.
SUPPLEMENTARY INFORMATION:
Preamble Acronyms and Abbreviation
We use multiple acronyms and terms in this preamble. While this
list may not be exhaustive, to ease the reading of this preamble and
for reference purposes, the EPA defines the following terms and
acronyms here:
ATSDR Agency for Toxic Substances and Disease Registry
BLDS bag leak detection system
BTF Beyond-the-Floor
CAA Clean Air Act
CBI Confidential Business Information
CFR Code of Federal Regulations
EJ environmental justice
EPA Environmental Protection Agency
ERPG Emergency Response Planning Guidelines
ERT Electronic Reporting Tool
FeMn Ferromanganese
FR Federal Register
HAP hazardous air pollutants
HCl hydrochloric acid
HI Hazard Index
HQ Hazard Quotient
ICR Information Collection Request
IRIS Integrated Risk Information System
km kilometer
MACT maximum achievable control technology
mg/dscm milligrams per dry standard cubic meter
mg/m\3\ milligrams per cubic meter
MIR maximum individual risk
MOR metal oxygen refining
MRL Minimal Risk Level
NAAQS National Ambient Air Quality Standards
NAICS North American Industry Classification System
NESHAP National Emissions Standards for Hazardous Air Pollutants
NTTAA National Technology Transfer and Advancement Act
OAQPS Office of Air Quality Planning and Standards
OECA Office of Enforcement and Compliance Assurance
OMB Office of Management and Budget
PAH polycyclic aromatic hydrocarbons
PB-HAP hazardous air pollutants known to be persistent and bio-
accumulative in the environment
PM particulate matter
POM polycyclic organic matter
REL reference exposure level
RFA Regulatory Flexibility Act
RfC reference concentration
RTR residual risk and technology review
SAB Science Advisory Board
SBA Small Business Administration
SiMn Silicomanganese
SSM startup, shutdown, and malfunction
TOSHI target organ-specific hazard index
TPY tons per year
TRIM.FaTE Total Risk Integrated Methodology.Fate, Transport, and
Ecological Exposure model
TTN Technology Transfer Network
[mu]g/dscm micrograms per dry standard cubic meter
[mu]g/m\3\ micrograms per cubic meter
UMRA Unfunded Mandates Reform Act
UPL Upper Prediction Limit
VCS voluntary consensus standards
Background Information
On November 23, 2011, and October 6, 2014, the EPA proposed
revisions to the Ferroalloys Production NESHAP based on our RTR. In
this action, we are finalizing decisions and revisions for the NESHAP.
We summarize some of the more significant comments we timely received
regarding the proposed rule and provide our responses in this preamble.
A summary of all other public comments on the proposal and the EPA's
responses to those comments are available in document titled: National
Emission Standards for Hazardous Air Pollutant Emissions: Ferroalloys
Production Summary of Public
[[Page 37367]]
Comments and the EPA's Responses on Proposed Rule (76 FR 72508,
November 23, 2011) and Supplemental Proposal (79 FR 60238, October 6,
2014), Docket ID No. EPA-HQ-OAR-2010-0895, which is available in the
docket. A ``track changes'' version of the regulatory language that
incorporates the changes in this action is also available in the
docket.
Organization of this Document. The information in this preamble is
organized as follows:
I. General Information
A. Does this action apply to me?
B. Where can I get a copy of this document and other related
information?
C. Judicial Review and Administrative Reconsideration
II. Background
A. What is the statutory authority for this action?
B. What is the Ferroalloys Production source category and how
does the NESHAP regulate HAP emissions from the source category?
C. What changes did we propose for the Ferroalloys Production
source category in our November 23, 2011, proposal and our October
6, 2014, supplemental proposal?
III. What is included in this final rule?
A. What are the final rule amendments based on the risk review
for the Ferroalloys Production source category?
B. What are the final rule amendments based on the technology
review for the Ferroalloys Production source category?
C. What are the final rule amendments pursuant to CAA section
112(d)(2) & (3) for the Ferroalloys Production source category?
D. What are requirements during periods of startup, shutdown,
and malfunction?
E. What other changes have been made to the NESHAP?
F. What are the effective and compliance dates of the standards?
G. What are the requirements for submission of performance test
data to the EPA?
IV. What is the rationale for our final decisions and amendments for
the Ferroalloys Production source category?
A. Residual Risk Review for the Ferroalloys Production Source
Category
B. Technology Review for the Ferroalloys Production Source
Category
C. CAA Section 112(d)(2) & (3) Revisions for the Ferroalloys
Production Source Category
D. What changes did we make to the Ferroalloys Production
opacity monitoring requirement?
V. Summary of Cost, Environmental, and Economic Impacts and
Additional Analyses Conducted
A. What are the affected sources?
B. What are the air quality impacts?
C. What are the cost impacts?
D. What are the economic impacts?
E. What are the benefits?
F. What analysis of environmental justice did we conduct?
G. What analysis of children's environmental health did we
conduct?
VI. Statutory and Executive Order Reviews
A. Executive Orders 12866: Regulatory Planning and Review and
Executive Order 13563: Improving Regulation and Regulatory Review
B. Paperwork Reduction Act (PRA)
C. Regulatory Flexibility Act (RFA)
D. Unfunded Mandates Reform Act (UMRA)
E. Executive Order 13132: Federalism
F. Executive Order 13175: Consultation and Coordination With
Indian Tribal Governments
G. Executive Order 13045: Protection of Children From
Environmental Health Risks and Safety Risks
H. Executive Order 13211: Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution or Use
I. National Technology Transfer and Advancement Act and 1 CFR
part 51
J. Executive Order 12898: Federal Actions To Address
Environmental Justice in Minority Populations and Low-Income
Populations
K. Congressional Review Act (CRA)
I. General Information
A. Does this action apply to me?
Regulated Entities. Categories and entities potentially regulated
by this action are shown in Table 1 of this preamble.
Table 1--NESHAP and Industrial Source Categories Affected by This Final
Action
------------------------------------------------------------------------
NAICS \a\
NESHAP and source category Code
------------------------------------------------------------------------
Ferroalloys Production.................................... 331112
------------------------------------------------------------------------
\a\ North American Industry Classification System.
Table 1 of this preamble is not intended to be exhaustive, but
rather to provide a guide for readers regarding entities likely to be
affected by the final action for the source category listed. To
determine whether your facility is affected, you should examine the
applicability criteria in 40 CFR part 63, subpart XXX (National
Emission Standards for Hazardous Air Pollutants (NESHAP): Ferroalloys
Production). If you have any questions regarding the applicability of
any aspect of this NESHAP, please contact the appropriate person listed
in the preceding FOR FURTHER INFORMATION CONTACT section of this
preamble.
B. Where can I get a copy of this document and other related
information?
In addition to being available in the docket, an electronic copy of
this final action will also be available on the Internet through the
Technology Transfer Network (TTN) Web site, a forum for information and
technology exchange in various areas of air pollution control.
Following signature by the EPA Administrator, the EPA will post a copy
of this final action at: https://www.epa.gov/ttn/atw/ferroa/ferropg.html. Following publication in the Federal Register, the EPA
will post the Federal Register version and key technical documents at
this same Web site.
Additional information is available on the RTR Web site at https://www.epa.gov/ttn/atw/rrisk/rtrpg.html. This information includes an
overview of the RTR program, links to project Web sites for the RTR
source categories and detailed emissions and other data we used as
inputs to the risk assessments.
C. Judicial Review and Administrative Reconsideration
Under CAA section 307(b)(1), judicial review of this final action
is available only by filing a petition for review in the United States
Court of Appeals for the District of Columbia Circuit by August 31,
2015. Under CAA section 307(b)(2), the requirements established by this
final rule may not be challenged separately in any civil or criminal
proceedings brought by the EPA to enforce the requirements.
Section 307(d)(7)(B) of the Clean Air Act (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 the EPA to reconsider the rule
``[i]f the person raising an objection can demonstrate to the
Administrator 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 should submit a Petition for Reconsideration to the
Office of the Administrator, U.S. EPA, Room 3000, EPA WJC 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.
[[Page 37368]]
II. Background
A. What is the statutory authority for this action?
Section 112 of the CAA establishes a two-stage regulatory process
to address emissions of HAP from stationary sources. In the first
stage, we must identify categories of sources emitting one or more of
the HAP listed in CAA section 112(b) and then promulgate technology-
based NESHAP for those sources. ``Major sources'' are those that emit,
or have the potential to emit, any single HAP at a rate of 10 tons per
year (tpy) or more, or 25 tpy or more of any combination of HAP. For
major sources, these standards are commonly referred to as maximum
achievable control technology (MACT) standards and must reflect the
maximum degree of emission reductions of HAP achievable (after
considering cost, energy requirements, and non-air quality health and
environmental impacts). In developing MACT standards, CAA section
112(d)(2) directs the EPA to consider the application of measures,
processes, methods, systems, or techniques, including, but not limited
to those that reduce the volume of or eliminate HAP emissions through
process changes, substitution of materials, or other modifications;
enclose systems or processes to eliminate emissions; collect, capture,
or treat HAP when released from a process, stack, storage, or fugitive
emissions point; are design, equipment, work practice, or operational
standards; or any combination of the above.
For these MACT standards, the statute specifies certain minimum
stringency requirements, which are referred to as MACT floor
requirements, and which may not be based on cost considerations. See
CAA section 112(d)(3). For new sources, the MACT floor cannot be less
stringent than the emission control achieved in practice by the best-
controlled similar source. For existing sources the MACT standards can
be less stringent than the floors for new sources, but they cannot be
less stringent than the average emission limitation achieved by the
best-performing 12 percent of existing sources in the category or
subcategory (or the best-performing five sources for categories or
subcategories with fewer than 30 sources). In developing MACT
standards, we must also consider control options that are more
stringent than the floor, under CAA section 112(d)(2). We may establish
standards more stringent than the floor, based on the consideration of
the cost of achieving the emissions reductions, any non-air quality
health and environmental impacts, and energy requirements.
In the second stage of the regulatory process, the CAA requires the
EPA to undertake two different analyses, which we refer to as the
technology review and the residual risk review. Under the technology
review, we must review the technology-based standards and revise them
``as necessary (taking into account developments in practices,
processes, and control technologies)'' no less frequently than every 8
years, pursuant to CAA section 112(d)(6). Under the residual risk
review, we must evaluate the risk to public health remaining after
application of the technology-based standards and revise the standards,
if necessary, to provide an ample margin of safety to protect public
health or to prevent, taking into consideration costs, energy, safety,
and other relevant factors, an adverse environmental effect. The
residual risk review is required within 8 years after promulgation of
the technology-based standards, pursuant to CAA section 112(f). In
conducting the residual risk review, if the EPA determines that the
current standards provide an ample margin of safety to protect public
health, it is not necessary to revise the MACT standards pursuant to
CAA section 112(f).\1\ For more information on the statutory authority
for this rule, see 79 FR 60238.
---------------------------------------------------------------------------
\1\ The U.S. Court of Appeals has affirmed this approach of
implementing CAA section 112(f)(2)(A); NRDC v. EPA, 529 F.3d 1077,
1083 (D.C. Cir. 2008) (``If EPA determines that the existing
technology-based standards provide an `ample margin of safety,' then
the Agency is free to readopt those standards during the residual
risk rulemaking.'').
---------------------------------------------------------------------------
B. What is the Ferroalloys Production source category and how does the
NESHAP regulate HAP emissions from the source category?
The EPA promulgated the Ferroalloys Production NESHAP on May 20,
1999 (64 FR 27450). The standards are codified at 40 CFR part 63,
subpart XXX. The ferroalloys production industry consists of facilities
that produce ferromanganese (FeMn) or silicomanganese (SiMn). The
source category covered by this MACT standard currently includes two
facilities.
The rule applies to ferroalloys production operations that are
located at major sources of HAP emissions or are co-located at a major
source of HAP emissions. The HAP emission sources at facilities subject
to the Ferroalloys Production NESHAP are open, semi-sealed, or sealed
submerged arc furnaces, tapping operations, casting operations, metal
oxygen refining (MOR) process, crushing and screening operations, other
processes, such as ladle treatment and slag raking, and outdoor
fugitive dust sources. The 1999 NESHAP regulated these emissions
sources through emission limits for PM, opacity limits, and work
practices.
C. What changes did we propose for the Ferroalloys Production source
category in our November 23, 2011, proposal and our October 6, 2014,
supplemental proposal?
On November 23, 2011, the EPA published a proposed rule in the
Federal Register (76 FR 72508) for the Ferroalloys Production NESHAP,
40 CFR part 63, subpart XXX that took into consideration the RTR
analyses. In the 2011 proposed rule, we proposed:
Revisions to the numeric emission limits for PM from
furnace stacks to reflect the current performance of control devices in
place at ferroalloys production facilities to control furnace emissions
(primary and tapping), crushing and screening operations, and the MOR
operation at one plant;
Addition of Hg, HCl, PAH, and formaldehyde furnace stack
emission standards that reflected the MACT determination for control of
these pollutants;
Requirements to capture process fugitive emissions using
full building enclosure with negative pressure building ventilation and
duct the captured emissions to a control device; and
Revisions to the opacity standards to reflect effective
capture and control of process fugitive emissions.
On October 6, 2014, the EPA published a supplemental proposed rule
in the Federal Register (79 FR 60238). For the supplemental proposal,
we proposed:
Revisions to the proposed PM furnace stack emission
standards based on additional test data submitted by the facilities;
Revisions to the proposed Hg, HCl, and PAH furnace stack
emission standards based on additional test data submitted by the
facilities;
Requirements to capture process fugitive emissions using
effective, enhanced local capture, and duct the captured emissions to
control devices;
Revisions to the opacity standards to reflect effective,
enhanced capture, and control of process fugitive emissions;
To demonstrate compliance with the opacity limits, we
proposed facilities would need to take opacity readings for an entire
furnace cycle once per week per furnace using Method 9 or
[[Page 37369]]
as an option they could take the readings using DCOT; and
Several minor clarifications and corrections.
III. What is included in this final rule?
This action finalizes the EPA's determinations pursuant to the RTR
provisions of CAA section 112 for the Ferroalloys Production source
category and amends the existing Ferroalloys Production NESHAP based on
those determinations. Among the changes finalized in this action are:
The promulgation of MACT-based limits for previously unregulated HAP;
requirements to effectively capture and control process fugitive
emissions; the removal of startup, shutdown, and malfunction (SSM)
exemptions; and the addition of DCOT monitoring. This action also
reflects several changes to the November 2011 and October 2014
proposals in consideration of comments received during the public
comment periods as described in section IV of this preamble.
A. What are the final rule amendments based on the risk review for the
Ferroalloys Production source category?
This section provides a summary of the final amendments to the
Ferroalloys Production NESHAP being promulgated pursuant to CAA section
112(f).
1. Stack Emissions
We are promulgating PM emission limits for stacks at the following
levels: 4.0 milligrams per dry standard cubic meter (mg/dscm) for new
or reconstructed electric arc furnaces; 25 mg/dscm for existing
electric arc furnaces; and 4.0 mg/dscm for any new, reconstructed, or
existing local ventilation control device. These emission limits are
the same as the limits proposed in the 2014 supplemental proposal.
In addition, we are promulgating a PM limit of 3.9 mg/dscm for any
new, reconstructed, or existing MOR process and a PM limit of 13 mg/
dscm for any new, reconstructed, or existing crushing and screening
equipment, which are consistent with what we proposed in our November
23, 2011, proposal.
2. Process Fugitive Emissions Sources
We are promulgating a requirement that facilities in this source
category must achieve effective enhanced capture of process fugitive
emissions using a system of primary hoods (that capture process
fugitive emissions near the source) and/or secondary capture of
fugitives (which would capture remaining fugitive emissions near the
roof-line). Facilities must install, operate, and maintain a process
fugitives capture system that is designed to capture 95 percent or more
of the process fugitive emissions. We are also promulgating an opacity
limit of 8-percent to ensure process fugitive emissions are effectively
captured. This is what we proposed in the October 6, 2014, supplemental
proposal. However, we have revised the rule based on public comment, to
provide more flexibility on how facilities achieve 95-percent capture
of process fugitive emissions. We also strengthened the monitoring
provisions to ensure that the required reductions are achieved.
B. What are the final rule amendments based on the technology review
for the Ferroalloys Production source category?
We determined that there are developments in practices, processes,
and control technologies that warrant revisions to the MACT standards
for this source category for both stack PM emissions and process
fugitive emissions. Therefore, under the authority of CAA section
112(d)(6), we are promulgating the same PM stack emission limits and
enhanced fugitive control requirements that we are promulgating under
CAA section 112(f), as described in section A above.
C. What are the final rule amendments pursuant to CAA section 112(d)(2)
& (3) for the Ferroalloys Production source category?
We are promulgating emission limits for formaldehyde, HCl, Hg, and
PAH, which were previously unregulated HAP, pursuant to CAA section
112(d)(2) and 112(d)(3).
We are promulgating a formaldehyde emission limit of 201 micrograms
per dry standard cubic meter ([mu]g/dscm) for any new, reconstructed,
or existing electric arc furnace. This is the same limit that we
proposed on November 23, 2011.
We are promulgating an HCl emission limit of 180 [mu]g/dscm for new
or reconstructed electric arc furnaces and 1,100 [mu]g/dscm for
existing electric arc furnaces. This is the same limit that we proposed
on October 6, 2014.
For electric arc furnaces producing FeMn, we are promulgating Hg
emission limits of 13 [mu]g/dscm for new or reconstructed electric arc
furnaces and 130 [mu]g/dscm for existing electric arc furnaces. For
electric arc furnaces producing SiMn, we are promulgating Hg emission
limits of 4 [mu]g/dscm for new or reconstructed electric arc furnaces
and 12 [mu]g/dscm for existing electric arc furnaces. The Hg limit for
new SiMn furnaces is the same as in the October 6, 2014, supplemental
proposal. The final Hg limits for new and existing FeMn and existing
SiMn furnaces are generally consistent with the supplemental proposal;
however, there were changes to these three limits due to the inclusion
of new emission data we received shortly before or during the
supplemental proposal comment period.
For electric arc furnaces producing FeMn, we are promulgating a PAH
emission limit of 12,000 [mu]g/dscm for new or reconstructed and
existing electric arc furnaces. The FeMn furnace PAH emission limits
are significantly higher than what we proposed in the October 6, 2014,
supplemental proposal due to the inclusion of new PAH emission data we
received a few weeks before signature of the supplemental proposal and
during the supplemental proposal comment period. We explained in the
supplemental proposal preamble that we received data shortly before
that notice and provided the data for comment (i.e., the data were
available in the docket). The data received during the comment period
were consistent with the data mentioned in the supplemental proposal.
For electric arc furnaces producing SiMn, we are promulgating a PAH
emission limit of 72 [mu]g/dscm for new or reconstructed electric arc
furnaces and 130 [mu]g/dscm for existing electric arc furnaces. The
SiMn furnace new PAH emission limit is the same as the limit in the
October 6, 2014, supplemental proposal. There was a slight revision to
the existing SiMn furnace PAH limit due to the inclusion of new
emission data we received during the supplemental proposal comment
period.
D. What are the requirements during periods of startup, shutdown and
malfunction?
We are finalizing, as proposed in the supplemental proposal,
changes to the Ferroalloys Production NESHAP to eliminate the SSM
exemption. Consistent with Sierra Club v. EPA 551 F. 3d 1019 (D.C. Cir.
2008), the EPA is establishing standards in this rule that apply at all
times. Table 1 to subpart XXX of part 63 (General Provisions
applicability table) is being revised to change several references
related to requirements that apply during periods of SSM. We also are
eliminating or revising certain recordkeeping and reporting
requirements related to the eliminated SSM exemption. The EPA also made
changes to the rule to remove or modify inappropriate, unnecessary, or
redundant language in the absence of the SSM exemption. We determined
that facilities in this source category can meet the applicable
emission standards
[[Page 37370]]
in the Ferroalloys Production NESHAP at all times, including periods of
startup and shutdown; therefore, the EPA determined that no separate
standards are needed to address emissions during these periods.
E. What other changes have been made to the NESHAP?
This rule also finalizes revisions to several other Ferroalloys
Production NESHAP requirements as proposed, or in some cases with some
modification as described in this section.
To increase the ease and efficiency of data submittal and data
accessibility, we are finalizing, as proposed, a requirement that
owners and operators of ferroalloys production facilities submit
electronic copies of certain required performance test reports through
an electronic performance test report tool called the Electronic
Reporting Tool (ERT). This requirement to submit performance test data
electronically to the EPA does not require any additional performance
testing and applies only to those performance tests conducted using
test methods that are supported by the ERT.
We are finalizing the opacity standards, as proposed in the
supplemental proposal. However, regarding compliance demonstration, we
are requiring that facilities measure opacity using DCOT. In the
supplemental proposal, we proposed facilities would need to monitor
opacity with Method 9 or DCOT. However, after considering public
comments, we decided to require DCOT rather than have it as optional.
Regarding monitoring frequency, we proposed facilities would need to do
opacity readings weekly per furnace building with no opportunity to
reduce frequency overtime. After considering public comments, we have
decided to require weekly readings initially, as proposed, but allow a
facility an opportunity to decrease frequency of opacity readings to
monthly per furnace building after 26 weeks of successful, compliant
opacity readings.
In addition, due to the large variation in PAH emissions from
furnace stacks during FeMn production, we are requiring quarterly
compliance tests for PAHs (i.e., four PAH compliance tests per year)
for furnaces while producing FeMn, with an opportunity for facilities
to request decreased frequency of such compliance testing from their
permit authority after the first year and after four or more successful
PAH compliance tests have been completed and submitted electronically.
We are also finalizing other minor changes to the NESHAP in
response to comments received during the public comment period for the
proposal and supplemental proposal, as described in this preamble.
F. What are the effective and compliance dates of the standards?
The revisions to the MACT standards being promulgated in this
action are effective on June 30, 2015. The compliance date for existing
ferroalloys production sources for all the requirements promulgated in
this final rule is June 30, 2017. Facilities must comply with the
changes set out in this final rule (which are being promulgated under
CAA sections 112(d)(2), 112(d)(3), 112(d)(6), and 112(f)(2) for all
affected sources) no later than 2 years after the effective date of the
final rule. CAA section 112(f)(4) generally provides that a standard
promulgated pursuant to CAA section 112(f)(2) applies 90 days after the
effective date, but further provides for a compliance period of up to 2
years when the Administrator determines that such time is necessary for
the installation of controls and that steps will be taken during that
period to assure protection to health from imminent endangerment. We
conclude that 2 years are necessary to complete the installation of the
enhanced local capture system and other controls. In the period between
the effective date of this rule and the compliance date, existing
sources will need to continue to comply with the requirements specified
in 40 CFR 63.1650 through 40 CFR 63.1660. New sources must comply with
the all of the standards immediately upon the effective date of the
standard, June 30, 2015, or upon startup, whichever is later.
G. What are the requirements for submission of performance test data to
the EPA?
As we proposed, the EPA is taking a step to increase the ease and
efficiency of data submittal and data accessibility. Specifically, the
EPA is finalizing the requirement for owners and operators of
ferroalloys production facilities to submit electronic copies of
certain required performance test reports.
Data will be collected by direct computer-to-computer electronic
transfer using EPA-provided software. This EPA-provided software is an
electronic performance test report tool called the ERT. The ERT will
generate an electronic report package which will be submitted to the
Compliance and Emissions Data Reporting Interface (CEDRI) and then
archived to the EPA's Central Data Exchange (CDX). A description and
instructions for use of the ERT can be found at https://www.epa.gov/ttn/chief/ert/ and CEDRI can be accessed through the CDX Web site
(https://www.epa.gov/cdx).
The requirement to submit performance test data electronically to
the EPA does not create any additional performance testing and will
apply only to those performance tests conducted using test methods that
are supported by the ERT. A listing of the pollutants and test methods
supported by the ERT is available at the ERT Web site. The EPA
believes, through this approach, industry will save time in the
performance test submittal process. Additionally, this rulemaking
benefits industry by reducing recordkeeping costs as the performance
test reports that are submitted to the EPA using CEDRI are no longer
required to be kept in hard copy.
State, local, and tribal agencies will benefit from more
streamlined and accurate review of performance test data that will
become available through WebFIRE. The public will also benefit. Having
these data publicly available enhances transparency and accountability.
For a more thorough discussion of electronic reporting of performance
tests using direct computer-to-computer electronic transfer and using
EPA-provided software, see the discussion in the preamble of the
proposal.
In summary, in addition to supporting regulation development,
control strategy development, and other air pollution control
activities, having an electronic database populated with performance
test data will save industry, state, local, tribal agencies, and the
EPA significant time, money, and effort while improving the quality of
emission inventories and air quality regulations and enhancing the
public's access to this important information.
IV. What is the rationale for our final decisions and amendments for
the Ferroalloys Production source category?
For each issue, this section provides a description of what we
proposed and what we are finalizing for the issue, the EPA's rationale
for the final decisions and amendments, and a summary of key comments
and responses. For all comments not discussed in this preamble, comment
summaries and the EPA's responses can be found in the comment summary
and response document, which is available in the docket.
[[Page 37371]]
A. Residual Risk Review for the Ferroalloys Production Source Category
1. What did we propose pursuant to CAA section 112(f) for the
Ferroalloys Production source category?
Pursuant to CAA section 112(f), we conducted a residual risk review
and presented the results of this review, along with our proposed
decisions regarding risk acceptability and ample margin of safety, in
the October 6, 2014, supplemental proposal for the Ferroalloys
Production NESHAP (79 FR 60238). The results of the risk assessment for
the 2014 supplemental proposal are presented briefly below in Table 2
and in more detail in the residual risk document, Residual Risk
Assessment for the Ferroalloys Source Category in Support of the
September 2014 Supplemental Proposal, which is available in the docket
for this rulemaking.
Based on actual emissions estimates for the Ferroalloys Production
source category supplemental proposal, the maximum individual risk
(MIR) for cancer was estimated to be up to 20-in-1 million driven by
emissions of chromium compounds, PAHs, and nickel compounds. The
maximum chronic non-cancer target organ-specific hazard index (TOSHI)
value was estimated to be up to 4 driven by fugitive emissions of
manganese. The maximum off-site acute hazard quotient (HQ) value was
estimated to be 1 for arsenic compounds, hydrogen fluoride (HF), and
formaldehyde. The total estimated national cancer incidence from this
source category, based on actual emission levels, was 0.002 excess
cancer cases per year, or one case in every 500 years.
Based on MACT-allowable emissions estimated for the Ferroalloys
Production source category supplemental proposal, the MIR was estimated
to be up to 100-in-1 million driven by emissions of arsenic and cadmium
compounds from the MOR process baghouse outlet. The maximum chronic
non-cancer TOSHI value was estimated to be up to 40 driven by emissions
of manganese from the MOR process. The total estimated national cancer
incidence from this source category, based on MACT-allowable emission
levels, was 0.005 excess cancer cases per year, or one case in every
200 years.
We also found there were emissions of four persistent and
bioaccumulative HAP (PB-HAP) with an available RTR multipathway
screening value, and the reported emissions of these four HAP (cadmium
compounds, dioxins/furans, Hg compounds, and PAH) were greater than the
Tier 1 multipathway screening values for these compounds for both
facilities at the time of the supplemental proposal. We conducted a
Tier 2 multipathway screen for both facilities, and conducted a refined
multipathway assessment for one facility in the source category.
Results of the refined multipathway assessment predict a potential
lifetime cancer risk of 10-in-1 million to the maximum exposed
individual due to exposure to dioxins and PAHs. The non-cancer HQ was
predicted to be below 1 for cadmium compounds and 1 for Hg compounds.
However, as explained in the Revised Development of the Risk and
Technology Review (RTR) Emissions Dataset for the Ferroalloys
Production Source Category for the 2014 Supplemental Proposal document,
it is important to note that about 75 percent of the emissions test
results for dioxins were below the detection limit. To be conservative,
in our calculations of emissions estimates, we assumed all the test
results that were recorded as below detection were one half the
detection limit. Therefore, there are considerable uncertainties in
estimated emissions for dioxins. Nevertheless, since we assumed
emissions were at the level of one half the detection limit in all
these cases where emissions were not even detected, we believe our
emissions estimates are conservative (i.e., more likely to be
overestimates rather than underestimates of the true emissions).
Emissions of the four PB-HAP and two environmental HAP (HCl and HF)
were reported by ferroalloys facilities. Tier 1 results for PB-HAP
indicate that concentrations of cadmium compounds and dioxins are below
the ecological benchmarks. Mercury compounds and PAHs concentrations
were greater than the benchmark so a Tier 2 screen was conducted. For
PAH and methylmercury, none of the individual modeled concentrations
for any facility exceeded any of the ecological benchmarks. For
mercuric chloride, the weighted average modeled concentrations for all
soil parcels were well below the soil benchmarks. For HCl and HF, the
average modeled concentrations around each facility did not exceed any
ecological benchmarks.
For the supplemental proposal, we weighed all health risk factors
in our risk acceptability determination and we proposed that the
residual risks from the Ferroalloys Production source category are
unacceptable.
Table 2--Ferroalloys Inhalation Risk Assessment Results in the October 2014 Supplemental Proposal
--------------------------------------------------------------------------------------------------------------------------------------------------------
Maximum individual cancer risk (in 1 million) Maximum chronic non-
\a\ cancer TOSHI \b\
---------------------------------------------- Estimated population at Estimated annual ----------------------------
increased risk levels of cancer incidence MACT- Maximum screening acute non-
MACT- allowable cancer (cases per year) Actual allowable cancer HQ \d\
Actual emissions level emissions emissions emissions
level \c\ level level
--------------------------------------------------------------------------------------------------------------------------------------------------------
20.......................... 100 >= 1-in-1 million: 31,000.. 0.002 4 40 HQREL = 1 (arsenic
>= 10-in-1 million: 400.... compounds, formaldehyde,
>= 100-in-1 million: 0..... hydrofluoric acid).
--------------------------------------------------------------------------------------------------------------------------------------------------------
\a\ Estimated maximum individual excess lifetime cancer risk due to HAP emissions from the source category.
\b\ Maximum TOSHI. The target organ with the highest TOSHI for the Ferroalloys Production source category for both actual and allowable emissions is the
neurological system. The estimated population at increased levels of noncancer hazard is 1,500 based on actual emissions and 11,000 based on allowable
emissions.
\c\ The development of allowable emission estimates can be found in the memorandum titled Revised Development of the RTR Emissions Dataset for the
Ferroalloys Production Source Category for the 2014 Supplemental Proposal, which is available in the docket.
\d\ See section III.A.3 of the supplemental proposal or the risk assessment document supporting the supplemental proposal for explanation of acute dose-
response values. Acute assessments are not performed on allowable emissions.
As described above, to address the unacceptable risks in the
supplemental proposal, we proposed tighter PM emission limits for the
stacks, which significantly reduce risks due to allowable emissions. To
reduce risks
[[Page 37372]]
due to process fugitive emissions, we proposed facilities must achieve
effective enhanced capture of process fugitive emissions using a system
of primary hoods (that capture process fugitive emissions near the
source) and/or secondary capture of fugitives (which would capture
remaining fugitive emissions near the roof-line). As described in the
supplemental proposal, we estimated that these controls would reduce
the MIR cancer risk estimate to 10-in-1 million and that the chronic
noncancer hazard index (HI) would be reduced to an HI of 1. Acute
screening and multipathway results were also reduced. In the
supplemental proposal, we concluded that these risks, after the
implementation of proposed controls, were acceptable.
We then considered whether the Ferroalloys Production NESHAP
provides an ample margin of safety to protect public health and whether
more stringent standards are necessary to prevent an adverse
environmental effect, taking into consideration costs, energy, safety,
and other relevant factors. In considering whether the standards should
be tightened to provide an ample margin of safety to protect public
health, we considered the same risk factors that we considered for our
acceptability determination and also considered the costs,
technological feasibility, and other relevant factors related to
emissions control options that might reduce risks associated with
emissions from the source category. Based on our ample margin of safety
analysis for the supplemental proposal, we did not identify any
additional cost-effective controls to further reduce risks beyond the
requirements we proposed to achieve acceptable risks. Therefore, we
proposed that additional HAP emissions controls are not necessary to
provide an ample margin of safety. Based on the results of our
screening analysis for risks to the environment, we also proposed that
more stringent standards are not necessary to prevent an adverse
environmental effect.
2. How did the risk review change for the Ferroalloys Production source
category?
Information received by the EPA shortly before and during the
supplemental proposal comment period included additional PAH and Hg
test data that were not included in the supplemental proposal risk
assessment due to timing and the need to review the data. We described
the data in the supplemental proposal and asked for comment on the use
of these data. After completion of the data review, these data were
included in the risk assessment for the final rule. Therefore, PAH and
Hg emissions estimates were revised for the final rule assessment. Some
revisions were also made for other HAP emissions. These changes are
discussed further in section IV of this preamble.
With the exception of the revised emissions described above, the
risk assessment supporting the final rule was conducted in the same
manner, using the same models and methods, as that conducted for the
supplemental proposal. The documentation for the final rule risk
assessment can be found in the document titled Residual Risk Assessment
for the Ferroalloys Source Category in Support of the 2015 Risk and
Technology Review Final Rule, which is available in the docket for this
rulemaking.
a. Inhalation Risk Assessment Results. Table 3 provides an overall
summary of the results of the inhalation risk assessment supporting the
final rule.
Table 3--Ferroalloys Inhalation Risk Assessment Results in the 2015 Final Rule
--------------------------------------------------------------------------------------------------------------------------------------------------------
Maximum individual cancer risk (in 1 million) Maximum chronic non-cancer
\a\ TOSHI \b\
---------------------------------------------- Estimated population at Estimated annual ----------------------------
increased risk levels of cancer incidence MACT- Maximum screening acute non-
MACT- allowable cancer (cases per year) Actual allowable cancer HQ \d\
Actual emissions level emissions level emissions emissions
\c\ level level
--------------------------------------------------------------------------------------------------------------------------------------------------------
20.......................... 100 >= 1-in-1 million: 41,000.. 0.003 4 40 HQREL = 1 (hydrofluoric
>= 10-in-1 million: 90..... acid, arsenic compounds).
>= 100-in-1 million: 0.....
--------------------------------------------------------------------------------------------------------------------------------------------------------
a Estimated maximum individual excess lifetime cancer risk due to HAP emissions from the source category.
b Maximum TOSHI. The target organ with the highest TOSHI for the Ferroalloys Production source category for both actual and allowable emissions is the
neurological system. The estimated population at increased levels of noncancer hazard is 1,300 based on actual emissions and 11,000 based on allowable
emissions.
c The development of allowable emission estimates can be found in the memorandum titled Revised Development of the RTR Emissions Dataset for the
Ferroalloys Production Source Category for the 2014 Supplemental Proposal, which is available in the docket.
d See section III.A.3 of the supplemental proposal or the risk assessment document supporting the supplemental proposal for explanation of acute dose-
response values. Acute assessments are not performed on allowable emissions.
The inhalation risk modeling performed to estimate risks based on
actual and allowable emissions for the final rule relied primarily on
updated emissions estimates based on data received through two
Information Collection Requests (ICRs), additional data submitted by
the companies voluntarily, and revised calculations as described
further in the Revised Development of the Risk and Technology Review
(RTR) Emissions Dataset for the Ferroalloys Production Source Category
for the 2015 Final Rule, which is available in the docket for this
action.
The results of the chronic baseline inhalation cancer risk
assessment indicate that, based on updated estimates of actual
emissions, the cancer MIR posed by the Ferroalloys Production source
category is 20-in-1 million, with chromium compounds, PAHs, and nickel
compounds from tapping fugitives, furnace fugitives, and furnace stacks
accounting for more than 70 percent of the MIR. The total estimated
cancer incidence from ferroalloys production sources based on updated
actual emission levels is 0.003 excess cancer cases per year, or one
case every 333 years, with emissions of PAH, chromium compounds, and
cadmium compounds contributing 49 percent, 15 percent, and 12 percent,
respectively, to this cancer incidence. In addition, we note that
approximately 90 people are estimated to have cancer risks greater than
or equal to 10-in-1 million, and approximately 41,000 people are
estimated to have risks greater than or equal to 1-in-1 million because
of actual emissions from this source category. These results, based on
updated actual
[[Page 37373]]
emissions, are very similar to those presented in the supplemental
proposal.
When considering the updated MACT-allowable emissions, the maximum
individual lifetime cancer risk is estimated to be up to 100-in-1
million, driven by emissions of arsenic and cadmium compounds from the
MOR process baghouse outlet. The estimated cancer incidence is
estimated to be 0.006 excess cancer cases per year or one excess case
in every 167 years. Approximately 3,300 people are estimated to have
cancer risks greater than or equal to 10-in-1 million and approximately
120,000 people are estimated to have cancer risks greater than or equal
to 1-in-1 million considering updated allowable emissions from
ferroalloys facilities. These results, based on updated MACT-allowable
emissions, are very similar to those presented in the supplemental
proposal.
The maximum modeled chronic non-cancer HI (TOSHI) value for the
source category based on updated actual emissions is estimated to be 4,
with manganese emissions from tapping fugitives accounting for more
than 50 percent of the HI. Approximately 1,300 people are estimated to
have exposure to HI levels greater than 1 as a result of updated actual
emissions from this source category. When considering updated MACT-
allowable emissions, the maximum chronic non-cancer TOSHI is estimated
to be 40, driven by manganese emissions from the MOR process baghouse
outlet. Approximately 12,000 people are estimated to have potential
exposure to TOSHI levels greater than 1 considering updated allowable
emissions from these ferroalloys facilities. These results, for both
updated actual and MACT-allowable emissions, are very similar to those
presented in the supplemental proposal.
b. Acute Risk Results. Based on the updated emissions described
above, our screening analysis for worst-case acute impacts based on
actual emissions indicates the potential for hydrofluoric acid and
arsenic compounds to have HQ results of 1, based on their respective
REL values. Both facilities have estimated acute HQs of 1 for these
pollutants. Acute HQs for other pollutants (e.g., hydrochloric acid)
are less than one. These acute results, based on updated emissions, are
very similar to those presented in the supplemental proposal.
All the HAP in this analysis have worst-case acute HQ values of 1
or less, indicating that they carry no potential to pose acute
concerns. In characterizing the potential for acute non-cancer impacts
of concern, it is important to remember the upward bias of these
exposure estimates (e.g., worst-case meteorology coinciding with a
person located at the point of maximum concentration during the hour)
and to consider the results along with the conservative estimates used
to develop peak hourly emissions as described earlier, as well as the
screening methodology. More discussion of our acute screening methods
can be found in the supplemental proposal or in the risk assessment
document, Residual Risk Assessment for the Ferroalloys Production
Source Category in Support of the 2015 Final Rule, which are available
in the docket.
c. Multipathway Risk Screening Results. Results of the worst-case
Tier I screening analysis indicate that PB-HAP emissions (based on
updated estimates of actual emissions) from one or both facilities in
this source category exceed the screening emission rates for cadmium
compounds, Hg compounds, dioxins, and PAHs. For the compounds and
facilities that did not screen out at Tier I, we conducted a Tier II
screen.
Based on the Tier II screening analysis, no facility emits cadmium
compounds above the Tier II screening levels. One facility emits Hg
compounds above the Tier II screening levels and exceeds that level by
a factor of 8. Both facilities emit chlorinated dibenzodioxins and
furans (CDDF) as 2,3,7,8-tetrachlorodibenzo-p-dioxin toxicity
equivalent (TEQ) above the Tier II screening levels and the facility
with the highest emissions of dioxins exceeds its Tier II screening
level by a factor of 10. Both facilities emit POM as benzo(a)pyrene TEQ
above the Tier II screening levels and the facility with the highest
emissions exceeds its screening level by a factor of 50. These
multipathway screening results, based on updated emissions, are very
similar to those presented in the supplemental proposal. More
information about our multipathway screening approach can be found in
the supplemental proposal or in the risk assessment document, Residual
Risk Assessment for the Ferroalloys Production Source Category in
Support of the 2015 Final Rule, which are available in the docket.
d. Multipathway Refined Risk Results. A refined multipathway
analysis was conducted for one of the two facilities in this source
category using the TRIM.FaTE model and the updated emissions as
described above. The facility, Eramet Marietta Incorporated, in
Marietta, Ohio, was selected based upon its close proximity to nearby
lakes, and farms as well as having the highest potential multipathway
risks for three of the four PB-HAP based on the Tier II analysis. In
addition, it was selected for a refined multipathway assessment in the
supplemental proposal. These three PB-HAP were cadmium, Hg, and PAHs.
Even though neither facility exceeded the Tier II screening levels for
cadmium, Eramet had the higher value. Eramet also emits dioxins, but
the other facility had a higher exceedance of its Tier II screening
level. The refined analysis was conducted on all four PB-HAP using
updated emissions as described above. The refined analysis for this
facility showed that the Tier II screen for each pollutant over-
predicted the potential risk when compared to the refined analysis
results.
Overall, the refined analysis predicts a potential lifetime cancer
risk of 20-in-1 million to the maximum most exposed individual due to
exposure to dioxins and PAHs. The non-cancer HQ is predicted to be
below 1 for cadmium compounds and 1 for Hg compounds. These results,
based on updated emissions, are very similar to those presented in the
supplemental proposal.
Further details on the refined multipathway analysis can be found
in Appendix 10 of the Residual Risk Assessment for the Ferroalloys
Production Source Category in Support of the 2015 Final Rule, which is
available in the docket.
e. Environmental Risk Screening Results. As described in section
III.A of the supplemental proposal preamble (79 FR 60238), we conducted
an environmental risk screening assessment for the Ferroalloys
Production source category. In the Tier I screening analysis for PB-HAP
(other than lead, which was evaluated differently as noted in section
III.A of the supplemental proposal preamble, 79 FR 60238), the
individual modeled Tier I concentrations for one facility in the source
category exceeded some sediment, fish-avian piscivorus, and surface
soil benchmarks for PAHs, methylmercury, and mercuric chloride.
Therefore, we conducted a Tier II assessment.
In the Tier II screening analysis for PAHs and methylmercury, none
of the individual modeled concentrations for any facility in the source
category exceeded any of the ecological benchmarks (either the lowest-
observed-adverse-effect level or the no-observed-adverse-effect level).
For mercuric chloride, soil benchmarks were exceeded for some
individual modeled points that collectively accounted for 11 percent of
the modeled area. However, the weighted average modeled concentration
for all soil parcels was well below the soil benchmarks. For
[[Page 37374]]
lead, we did not estimate any exceedances of the secondary lead
National Ambient Air Quality Standards (NAAQS).
For HCl, each individual concentration (i.e., each off-site data
point in the modeling domain) was below the ecological benchmarks for
all facilities. The average modeled HCl concentration around each
facility (i.e., the average concentration of all off-site data points
in the modeling domain) did not exceed any ecological benchmark. For
HF, some individual modeled points exceeded the ecological benchmark
but accounted for less than 0.02 percent of the modeled area. The
average modeled HF concentration around each facility (i.e., the
average concentration of all off-site data points in the modeling
domain) did not exceed any ecological benchmarks. These results, based
on updated emissions, are very similar to those presented in the
supplemental proposal.
f. Facility-Wide Risk Assessment Results. As in the supplemental
proposal, for both facilities in this source category, there are no
other HAP emissions sources present beyond those included in the source
category. Therefore, we conclude that the facility-wide risk is the
same as the source category risk and that no separate facility-wide
analysis is necessary.
g. Demographic Analysis Results. To examine the potential for any
environmental justice (EJ) issues that might be associated with the
source category, we updated the demographic analysis that was conducted
for the supplemental proposal, using the risk results based on the
updated emissions. A demographic analysis is an assessment of risks to
individual demographic groups of the population close to the
facilities. In this analysis, we evaluated the distribution of HAP-
related cancer risks and noncancer hazards from the Ferroalloys
Production source category across different social, demographic, and
economic groups within the populations living near facilities
identified as having the highest risks. The methodology and the results
of the demographic analyses are included in a technical report, Risk
and Technology Review--Analysis of Socio-Economic Factors for
Populations Living Near Ferroalloys Facilities, which is available in
the docket for this action.
The results of the demographic analysis are summarized in Table 4
below. These results, for various demographic groups, are based on the
estimated risks from actual emissions levels for the population living
within 50 kilometers (km) of the facilities.
Table 4--Ferroalloys Production Demographic Risk Analysis Results for 2015 Final Rule
----------------------------------------------------------------------------------------------------------------
Population with
cancer risk at or Population with
above 1-in-1 chronic hazard
Nationwide million due to index above 1 due
Ferroalloys to Ferroalloys
Production Production
----------------------------------------------------------------------------------------------------------------
Total Population....................................... 312,861,265 40,748 1,348
----------------------------------------------------------------------------------------------------------------
Race by Percent
----------------------------------------------------------------------------------------------------------------
White.................................................. 72 97 99
All Other Races........................................ 28 3 1
----------------------------------------------------------------------------------------------------------------
Race by Percent
----------------------------------------------------------------------------------------------------------------
White.................................................. 72 97 99
African American....................................... 13 1 0
Native American........................................ 1 0 0
Other and Multiracial.................................. 14 2 1
----------------------------------------------------------------------------------------------------------------
Ethnicity by Percent
----------------------------------------------------------------------------------------------------------------
Hispanic............................................... 17 1 1
Non-Hispanic........................................... 83 99 99
----------------------------------------------------------------------------------------------------------------
Income by Percent
----------------------------------------------------------------------------------------------------------------
Below Poverty Level.................................... 14 15 6
Above Poverty Level.................................... 86 85 94
----------------------------------------------------------------------------------------------------------------
Education by Percent
----------------------------------------------------------------------------------------------------------------
Over 25 and without High School Diploma................ 15 11 10
Over 25 and with a High School Diploma................. 85 89 90
----------------------------------------------------------------------------------------------------------------
Age by Percent
----------------------------------------------------------------------------------------------------------------
Ages 0 to 17........................................... 24 21 22
Ages 18 to 64.......................................... 63 61 59
Ages 65 and up......................................... 13 18 19
----------------------------------------------------------------------------------------------------------------
The results of the Ferroalloys Production source category
demographic analysis indicate that emissions from the source category
expose approximately 41,000 people to a cancer risk at or above 1-in-1
million and approximately 1,300 people to a chronic non-cancer TOSHI
greater than 1 (we note that many of those in the first risk group are
the same as those in the second). The percentages of the at-risk
population in each demographic group
[[Page 37375]]
(except for ages 65 and up) are similar to or lower than their
respective nationwide percentages. These results are very similar to
those presented in the supplemental proposal.
3. What key comments did we receive on the risk review, and what are
our responses?
Several comments were received regarding the risk assessment for
the Ferroalloys Production source category. The following is a summary
of some of the more significant comments and our responses to those
comments. Other comments received and our responses to those comments
can be found in the document titled National Emission Standards for
Hazardous Air Pollutant Emissions: Ferroalloys Production Summary of
Public Comments and the EPA's Responses on Proposed Rule (76 FR 72508,
November 23, 2011) and Supplemental Proposal (79 FR 60238, October 6,
2014), which is available in the docket for this action (EPA-HQ-OAR-
2010-0895).
Comment: Several comments were received on the reference value used
in the risk assessment to evaluate chronic noncancer effects due to
exposure to manganese. In the 2011 proposal, we used the Integrated
Risk Information System (IRIS) reference concentration (RfC), and we
received negative comments regarding that value not being the ``best
available science.'' We evaluated the available values and, in
accordance with our prioritized dose-response values and Scientific
Advisory Board (SAB) comments, we used the Agency for Toxic Substances
and Disease Registry (ATSDR) minimum risk level (MRL) for manganese in
the risk assessment for the 2014 supplemental proposal. We received
mixed comments in response to the supplemental proposal. Some comments
were negative regarding our use of the ATSDR MRL, while others were
generally supportive of our use of the MRL compared to the IRIS value,
yet still thought the MRL was not the appropriate reference value to
use in the assessment.
Regarding use of the IRIS RfC for manganese in the 2011 proposal
risk assessment, commenters stated that the manganese RfC was outdated,
did not constitute the best available science (including use of
benchmark dose statistical analyses or physiologically-based
pharmacokinetic models), and substantial research has been conducted
since the 1993 IRIS RfC was last updated. The commenters refer to their
own calculations and studies and developed their own reference value
for manganese and state that the EPA should use that value. Regarding
use of the ATSDR MRL for manganese in the 2014 supplemental proposal
risk assessment, the same commenters stated that the manganese MRL was
an improvement over the IRIS RfC, but was still not the best available
science because, in their review, ATSDR did not apply physiologically-
based pharmacokinetic models. The commenters again refer to their own
calculations and studies developing a reference value for manganese and
state that EPA should use that value. Another commenter disagrees with
the use of the ATSDR MRL because the EPA has not provided sufficient
rationale for using a less-protective value. Instead, this commenter
recommended that we continue to use the IRIS RfC value.
Response: We agree that there were newer information and
assessments available at the time of the 2011 proposal and also for the
2014 supplemental proposal, some of which may use the currently
preferred approach for developing dose-response values (i.e., the
benchmark dose approach). However, we only use reference values which
meet certain criteria in regards to how they are derived (using EPA
guidelines or similar), derived by credible sources with health-
protective goals similar to those of the EPA, using peer-review
procedures also similar to the level applied to the EPA values, and
with an open public comment process. We have a tiered priority list for
sources of chronic dose-response information, which meet these criteria
(as described in the supplemental proposal, 79 FR 60238). The tiered
prioritized list has been through a SAB review and was favorably
received.
In the risk assessment for the 2011 proposal, we used the IRIS RfC
for chronic exposure to manganese and received numerous comments
regarding use of that value. In response to those comments, we
considered the existing peer-reviewed health effect reference values
for chronic inhalation exposure to manganese from other federal, state,
and international agencies and organizations. We developed a reference
value array document \2\ providing additional details for the available
values. We noted that the ATSDR MRL value available for the 2011
proposal was a draft value. The ATSDR MRL was subsequently finalized in
2012.
---------------------------------------------------------------------------
\2\ U.S. EPA. Mn and BTEX Reference Value Arrays (Final
Reports). U.S. Environmental Protection Agency, Washington, DC, EPA/
600/R-12/047F, 2013.
---------------------------------------------------------------------------
In our consideration of available reference values, we did not
include some values specifically noted in public comments. The level of
peer review for non-governmental scientific publications is
qualitatively different than the governmental processes used to derive
the values described in our tiered prioritized list, and some of the
values in the manganese reference value array document. The information
provided by these additional references from the commenter(s) may prove
useful in an IRIS reassessment for manganese, and we agree that the
physiologically-based models, along with all other relevant available
peer-reviewed literature, will be considered in any IRIS reassessment
of manganese. Yet, a direct application of any of these values instead
of an established value in our tiered list of prioritized dose-response
values would be inconsistent with the EPA policy as implemented in the
RTR Program, and with recommendations from the SAB.
After considering the values in our tiered list of prioritized
dose-response values, and consistent with Agency policy supported by
SAB, we decided to rely on the 2012 ATSDR MRL value for the 2014
supplemental proposal. Both the 1993 IRIS RfC and the 2012 ATSDR MRL
were based on the same study (Roels et al., 1993). In developing their
assessment, ATSDR used updated dose-response modeling methodology
(benchmark dose approach) and considered recent pharmacokinetic
findings to support their selection of uncertainty values in the MRL
derivation.
4. What is the rationale for our final approach and final decisions for
the risk review?
As noted in section II.A.1 of this preamble, the EPA sets standards
under CAA section 112(f)(2) using ``a two-step standard-setting
approach, with an analytical first step to determine an `acceptable
risk' that considers all health information, including risk estimation
uncertainty and includes a presumptive limit on maximum individual
lifetime risk (MIR) of approximately 1 in 10 thousand.'' \3\ (54 FR
38045, September 14, 1989).
---------------------------------------------------------------------------
\3\ 1-in-10 thousand is equivalent to 100-in-1 million. The EPA
currently describes cancer risks as `n-in-1 million.'
---------------------------------------------------------------------------
a. Acceptability Determination. As in the supplemental proposal,
the EPA concludes that the risks are unacceptable for the following
reasons. First, the EPA considered the fact that the noncancer hazard
HQ ranges from 4 based on actual emissions to 40 based on allowable
emissions. The EPA has not established under section 112 of the CAA a
numerical range for risk
[[Page 37376]]
acceptability for noncancer effects as it has with carcinogens, nor has
it determined that there is a bright line above which acceptability is
denied. However, the Agency has established that, as exposure increases
above a reference level (as indicated by a HQ or TOSHI greater than 1),
confidence that the public will not experience adverse health effects
decreases and the likelihood that an effect will occur increases. For
the Ferroalloys Production source category, the potential for members
of the public to be exposed to manganese at concentrations up to 40
times the MRL reduces the Agency's confidence that the public is
protected from adverse health effects and diminished the Agency's
ability to determine that such exposures are acceptable. Second, the
EPA considered the fact that the cancer risk estimate for actual
emissions is 20-in-1 million and up to 100-in-1 million for allowable
emissions. While 20-in-1 million is well within the acceptable range,
risks from allowable emissions are at the upper end of the range of
acceptability. This fact, combined with the fact that the noncancer
hazard is up to 40 times the MRL and the refined multipathway HQ for Hg
is at the RfD, leads the Agency to conclude that the risk from this
source category is unacceptable.
b. What is EPA requiring in the final rule to address the
unacceptable risks? As mentioned above, to address the unacceptable
risks, we are promulgating tighter PM emission limits for the stacks,
which significantly reduces risks due to allowable emissions.
Furthermore, to reduce risks due to process fugitive emissions, we are
promulgating a requirement that facilities must achieve effective
enhanced capture of process fugitive emissions using a system of
primary hoods (that capture process fugitive emissions near the source)
and/or secondary capture of fugitives (which would capture remaining
fugitive emissions near the roof-line). Facilities must install,
operate, and maintain a process fugitives capture system that is
designed to capture and control 95 percent or more of the process
fugitive emissions. We are also promulgating an opacity limit of 8
percent to ensure process fugitive emissions are effectively captured
and controlled. Facilities will need to meet an average opacity of 8
percent for the entire furnace cycle (about 90-120 minutes) with a
maximum opacity of no more than 20-percent opacity for any 12-minute
period. Moreover, facilities will need to monitor various control
parameters (such as fan speed, amperage, pressure drops, and/or damper
positioning) to ensure the process fugitive capture systems and
controls are working properly.
c. Remaining Risks After Implementation of the Requirements to
Address Unacceptable Risks. To determine the remaining risks after
implementation of the lower stack PM emissions limits and requirements
to effectively control process fugitives (described above), we
conducted a post control risk assessment, which is described in detail
in the document titled Residual Risk Assessment for the Ferroalloys
Source Category in Support of the 2015 Final Rule, which is available
in the docket for this rulemaking.
Based on this post control risk assessment, we conclude that after
the requirements described above to address unacceptable risks are
implemented, the risks to public health will be substantially reduced.
For example, the results of the post-control chronic inhalation
cancer risk assessment indicate that the maximum individual lifetime
cancer risk posed by these two facilities, after the implementation of
the promulgated controls, will be no higher than 10-in-1 million, with
an estimated reduction in cancer incidence to 0.002 cases per year. In
addition, the number of people estimated to have a cancer risk greater
than or equal to 1-in-1 million would be 26,000. The results of the
post-control risk assessment also indicate that the maximum chronic
noncancer inhalation TOSHI value would be reduced to 1. The number of
people estimated to have a TOSHI greater than 1 would be reduced to 0.
We also estimate that after the implementation of controls, the maximum
worst-case acute HQ value would be less than 1 (based on REL values).
Considering post-control emissions of multipathway HAP, Hg
emissions would be reduced by approximately 3 pounds per year (lbs/yr),
lead would be reduced by about 1,600 lbs/yr, polycyclic organic matter
(POM) emissions would be reduced by approximately 3,600 lbs/yr, cadmium
would be reduced by about 150 lbs/yr, and dioxins and furans would be
reduced by about 0.002 lbs/yr from the baseline emission rates.
d. Ample Margin of Safety Analysis. Under the ample margin of
safety analysis, we again considered all of the health factors
evaluated in the acceptability determination and evaluated the cost and
feasibility of available control technologies and other measures
(including the controls, measures, and costs reviewed under the
technology review) that could be applied in this source category to
further reduce the risks due to emissions of HAP identified in our risk
assessment.
As described above, we estimate that the actions finalized under
CAA section 112(f)(2) to address unacceptable risks will reduce the MIR
to 10-in-1 million. The cancer incidence will be reduced to 0.002 cases
per year and the number of people estimated to have cancer risks
greater than 1-in-1 million will be reduced to 26,000 people. The
chronic noncancer inhalation TOSHI will be reduced to 1 and the number
of people exposed to a TOSHI level greater than 1 will be reduced to 0.
In addition, the potential multipathway impacts will be reduced.
Based on all of the above information, we conclude that the risks
will be acceptable after implementation of the lower stack limits for
PM and the control requirements to reduce process fugitive emissions,
as we concluded in the supplemental proposal. Based on our research and
analysis, we did not identify any cost-effective controls beyond those
described above that would achieve further reduction in risk. While in
theory, the 2011 proposed approach of total enclosure with negative
pressure would provide some additional risk reduction, the additional
risk reduction is minimal and, similar to our assessment and
conclusions described in the supplemental proposal, we continue to
believe the total enclosure approach would not be economically feasible
and may not be technically feasible for these facilities. No other
technology advances were identified during the comment period.
Therefore, we are not promulgating any additional requirements under
the ample margin of safety analysis beyond the requirements being
finalized to address unacceptable risks (as described above). We
conclude that the controls to achieve acceptable risks will also
provide an ample margin of safety to protect public health.
B. Technology Review for the Ferroalloys Production Source Category
1. What did we propose pursuant to CAA section 112(d)(6) for the
Ferroalloys Production source category?
Pursuant to CAA section 112(d)(6), we conducted a technology
review, which focused on identifying and evaluating developments in
practices, processes, and control technologies for the emission sources
in the Ferroalloys Production source category. For the 2011 proposal
(76 FR 72508), we
[[Page 37377]]
identified developments in practices, processes or control technologies
for PM emissions from stacks (as a surrogate for metal HAP) and for
process fugitive metal HAP emissions. Based on the comments received
from the public and information received through a 2012 ICR, we revised
both the technology review and risk assessment for the Ferroalloys
Production source category, which were described in detail in the 2014
supplemental proposal (79 FR 60238).
a. PM Emission Limits From Stacks. For PM stack emissions limits,
we determined for the 2011 proposal that the test data received from
the two facilities indicate that all five furnaces that are in
operation have PM emission levels that are well below their respective
emission limits in the 1999 MACT rule, which were based on size and
product being produced. The test data received from the facilities also
indicate that the PM emission levels for MOR and crushing and sizing
are well below their respective emission limits in the 1999 MACT rule.
These findings demonstrate that add-on particulate control technologies
(Venturi scrubber, positive pressure fabric filter, negative pressure
fabric filter) used to control emissions from the sources are effective
in reducing PM (used as a surrogate for metal HAP). Based on these
findings, in 2011 we proposed a PM limit of 24 mg/dscm corrected to 2
percent carbon dioxide (CO2) for existing furnaces.
We received additional test data after the 2011 proposal and re-
evaluated the PM limit using available PM emissions test data and
consideration of variability across these data. Based on this analysis,
we determined that it was appropriate to propose a revised PM limit of
25 mg/dscm for existing furnaces. No additional add-on control is
expected to be required by the facilities to meet this revised existing
source limit. To demonstrate compliance, we proposed these sources
would be required to conduct periodic performance testing and develop
and operate according to a baghouse operating plan or continuously
monitor Venturi scrubber operating parameters. We also proposed that
furnace baghouses would be required to be equipped with bag leak
detection systems (BLDS).
For the 2011 proposal, the proposed new source PM standard was
determined by evaluating the available data from the best performing
furnace (which was determined to be furnace #2 at Felman). The proposed
new source limit was determined to be 9.3 mg/dscm. We received
additional test data after the 2011 proposal and re-evaluated the new
source limit using the available test data. The revised new source PM
standard for furnaces for the 2014 supplemental proposal was determined
by evaluating the available data from the best performing furnace
(which was again determined to be furnace #2 at Felman). The new source
MACT limit was determined to be 4.0 mg/dscm based on data from furnace
#2 and was proposed as the MACT emissions limit for PM from new and
reconstructed source furnace stacks in the 2014 supplemental proposal.
The PM emission limit for the local ventilation control device
outlet was also re-evaluated using compliance test data and test data
from the 2012 ICR. A local ventilation control system is used to
capture tapping, casting, or ladle treatment emissions and direct them
to a control device other than one associated with the furnace. The
2011 proposal included a proposed PM limit for the local ventilation
control device that was based on PM data from the furnaces. After the
2011 proposal, we received test data from three different emissions
tests (for a total of nine test runs) specifically for this local
ventilation source. We determined these data were more appropriate for
the development of a limit for this source than the furnace data we had
used for the 2011 proposal. There is currently only one local
ventilation control device outlet emissions source in this source
category. Using the new data for the one existing local ventilation
source, we calculated a revised emissions limit of 4.0 mg/dscm and
determined that this was an appropriate emissions limit for this
source. Therefore, we proposed an emissions limit of 4.0 mg/dscm for
existing, new, and reconstructed local ventilation control device
emissions sources in the supplemental proposal.
For crushing and screening operations, we proposed an emission
limit of 13 mg/dscm for new and existing crushing and sizing operations
in the 2011 proposal. We did not receive any additional data for this
emission source and, therefore, made no revisions to this proposed
limit in the 2014 supplemental proposal.
The MOR operation is a unique process that is operated by only one
facility (Eramet). We calculated a proposed emission limit of 3.9 mg/
dscm in the 2011 proposal that would apply to both new and existing MOR
operation sources. We did not receive any additional data for this
emission source and, therefore, made no revisions to this proposed
limit in the 2014 supplemental proposal.
b. Emission Standards for Process Fugitives. For process fugitive
metal HAP emissions, we identified two potential developments in
practices and control techniques. One option would require facilities
to install and operate enhanced capture of process fugitive emissions
using a combination of primary hoods and ductwork in close proximity to
the emission sources, such as tapping or casting and/or secondary hoods
located near the roofline. Another option would be to require full
enclosure of the furnace building(s) with negative pressure and
evacuate the process fugitive emissions to a control device(s). In the
2011 proposal, we proposed that the full furnace building enclosure
option represented an advance in emission control measures since the
Ferroalloys Production NESHAP was originally promulgated in 1999.
For day-to-day continuous monitoring to demonstrate compliance with
the proposed full building enclosure requirements, the 2011 proposal
relied mainly on requiring monitoring differential pressure to ensure
facilities maintained a negative pressure of at least 0.007 inches of
water and that emissions within the facilities would need to be vented
to PM control devices. This was to be supplemented by operation and
work practice standards that required preparation of a process fugitive
emissions ventilation plan for each shop building. In the 2011
proposal, we also proposed a requirement that emissions exiting from a
shop building may not exceed more than 10-percent opacity for more than
one 6-minute period, to be demonstrated every 5 years as part of the
periodic required performance tests.
We received significant comments in response to the 2011 proposal.
Commenters claimed that we had significantly underestimated the costs
for full building enclosure and that it would not be feasible for these
facilities. After reviewing and considering the comments along with
other information, we decided to re-evaluate the proposed requirement
for negative pressure ventilation and consider other options.
Based on our re-evaluation, for the 2014 supplemental proposal, we
concluded that the full-building enclosure option may not be feasible
and would have significant economic impacts on the facilities. However,
we concluded that an option based on enhanced local capture and control
of process fugitive emissions using a combination of primary and
secondary hoods is a feasible and cost-effective approach to achieve
significant reductions in process fugitive HAP emissions. Therefore, in
the 2014 supplemental proposal, we proposed
[[Page 37378]]
that facilities would need to install and operate a local capture
system using a combination of primary and/or secondary hoods that is
designed to achieve at least 95-percent capture and control of process
fugitive emissions.
With the move to the proposed enhanced local capture alternative in
the 2014 supplemental proposal, we no longer had a day-to-day
continuous requirement of monitoring negative pressure. Instead, in the
2014 supplemental proposal, continuous compliance demonstration would
be based mainly on meeting an opacity limit, monitoring ventilation
parameters (such as fan speed, amperage, and/or damper positioning),
and documenting the design of the system to achieve 95-percent capture.
Since opacity monitoring would be a primary method to demonstrate
continuous compliance, we proposed that facilities would need to meet
an average opacity of 8 percent for an entire furnace cycle (about 90-
120 minutes) with a maximum opacity of no more than 20 percent opacity
for any 12-minute period. Furthermore, we proposed facilities would
need to monitor opacity for a full furnace cycle (about 90-120 minutes)
at least once per week per furnace building. We also proposed that, if
the average opacity reading from the shop building is greater than 8-
percent opacity during an observed furnace process cycle, an additional
two more furnace process cycles must be observed such that the average
opacity during the entire observation period is less than 7-percent
opacity. A furnace process cycle means the period in which the furnace
is tapped to the time in which the furnace is tapped again and includes
periods of charging, smelting, tapping, casting, and ladle raking.
Regarding the design requirements, in the supplemental proposal, we
proposed that the facilities in this source category must install,
operate, and maintain a process fugitives capture system that is
designed to collect 95 percent or more of the process fugitive
emissions from furnace operations, casting MOR process, ladle raking,
and slag skimming and crushing and screening operations and convey the
collected emissions to a control device that meets specified emission
limits and the proposed opacity limits. We proposed that this plan be
submitted to the permitting authority, incorporated into the source's
operating permit and updated every 5 years or when there is a
significant change in variables that affect process fugitive emissions
ventilation design. We proposed that this list of design criteria,
coupled with the requirement for frequent opacity observations and
operating parameter monitoring, would ensure process fugitive emissions
are effectively controlled and would result in enforceable
requirements.
More information concerning our proposed technology review can be
found in the memoranda titled, Revised Technology Review for the
Ferroalloys Production Source Category, and Cost Impacts of Control
Options Considered for the Ferroalloys Production NESHAP to Address
Fugitive HAP Emissions, which are available in the docket, and in the
preamble to the 2014 supplemental proposed rule, 79 FR at 60271 to
60273.
2. How did the technology review change for the Ferroalloys Production
source category?
For the October 6, 2014, supplemental proposal, we solicited
comment regarding the use of new technologies to provide continuous or
near continuous long term approaches to monitoring emissions from
industrial sources for the Ferroalloy Production source category. After
considering comments received and after evaluating the technologies
further, we are replacing the weekly Method 9 opacity requirement with
a weekly requirement to measure opacity using ASTM D7520-13 and DCOT to
demonstrate compliance with the process fugitives standards. The final
rule amendments require facilities to use the DCOT to measure opacity
at least once per week for each of the furnace and MOR buildings to
demonstrate compliance with the opacity limits. However, as mentioned
above, facilities will have the opportunity to reduce the frequency of
opacity readings to monthly after 26 consecutive weeks of compliant
weekly readings. The facilities would still be required to meet an
average opacity standard of 8-percent opacity for the furnace cycle
(90-120 minutes) and at no time during operation may any two
consecutive 6-minute block opacity readings be greater than 20-percent
opacity. The cost of implementing the DCOT system is estimated to be
approximately $200,000 per year for the source category with weekly
readings. However, these costs decrease to about $90,000 per year for
the source category if they do monthly readings per furnace building.
All other requirements we proposed under CAA section 112(d)(6) in the
supplemental proposal have not changed.
3. What key comments did we receive on the technology review, and what
are our responses?
Several comments were received regarding the technology review for
the Ferroalloys Production source category. The following is a summary
of the more significant comments and our responses to those comments.
Other comments received and our responses to those comments can be
found in the document titled National Emission Standards for Hazardous
Air Pollutant Emissions: Ferroalloys Production Summary of Public
Comments and the EPA's Responses on Proposed Rule (76 FR 72508,
November 23, 2011) and Supplemental Proposal (79 FR 60238, October 6,
2014), which is available in the docket for this action (EPA-HQ-OAR-
2010-0895).
Comment: One commenter supported the EPA's decision to re-evaluate
the feasibility and cost-effectiveness of the controls that the Agency
proposed in its 2011 proposal. However, the commenter objects to the
EPA's conclusion that an alternative system involving both primary and
secondary capture is available and represents an ``advancement in
technology'' pursuant to CAA section 112(d)(6). The commenter states
that this type of system does not currently exist in practice at any
ferroalloy operation. They explain that, in theory, such a system
appears likely to provide some degree of additional reductions.
However, the commenter notes some of the specific potential control
methods mentioned by the EPA have already been proven not to work. As
an example, the commenter states that curtains have previously been
installed in an attempt to contain additional furnace emissions, but
the curtains burned up due to the extreme heat in only a few weeks. The
commenter, therefore, objects both to the characterization of these
additional controls as a currently available ``advancement in
technology,'' and to the EPA's conclusion that the cost of almost
$100,000 per ton of HAP reductions for these additional controls is
cost effective.
Response: In their supplemental comments on the 2011 proposed rule,
industry representatives provided suggested alternative designs to
address fugitive emissions from the furnace buildings. The designs
suggested by the industry representatives included improving the
existing primary hooding and capture systems close to the emissions
sources and/or adding secondary capture to ensure effective capture and
control of process fugitive
[[Page 37379]]
emissions. The use of a primary hooding and exhaust system in
conjunction with general secondary hooding and exhaust system was
estimated to provide a total capture of 95 percent of process fugitive
emissions, including emissions from the tapping, casting, crushing/
screening, and skimming/slag raking processes.
We reviewed these designs and discussed the designs with
ventilation experts. The ventilation experts agreed that the suggested
primary system along with secondary capture could achieve 95 percent
reduction of process fugitive emissions from the buildings. They noted
that many of the designs and improvements were based on the elements of
good ventilation systems that are used in other industries to capture
and control fugitive emissions. Because these designs have been only
partially deployed in this industry, they constitute a relevant
development in technology beyond what is required by the current rule.
We view the successful deployment of these technologies in other
industries and the expert judgement of industrial ventilation experts
as establishing that the technologies are technically available for
transfer to the Ferroalloy Production source category.
As part of our technology review, we evaluated the costs and
effectiveness of a regulatory option that is based on the general
emission control scenario suggested by the industry representatives
which would include a system of primary and/or secondary hooding
designed to capture 95 percent of process fugitive emissions. The
process fugitive emissions would be captured by the primary and/or
secondary hoods and routed to PM control devices. This option for the
control of process fugitive emissions under CAA section 112(d)(6) is
exactly the same option that we are promulgating under CAA section
112(f)(2) to capture and control fugitives (described in section IV.A
of this preamble). We estimate that the total capital cost including
monitoring would be about $40.3 million, the total annualized costs
would be about $7.7 million per year, and that it would achieve 77 tpy
reduction of HAP, mostly manganese and other HAP metals (e.g., cadmium
compounds, chromium compounds, nickel compounds) and also achieve about
229 tpy reduction of PM. Based on our evaluation, we conclude that
installing and operating such a system is a feasible and cost-effective
approach to achieve significant reductions in process fugitive HAP
emissions and will achieve almost as much reductions as the full
building enclosure option (229 vs. 252 tons PM reductions). In light of
the technical feasibility and cost effectiveness of this enhanced
fugitive capture option (that includes a combination of primary capture
and/or secondary capture designed to capture and control 95 percent of
process fugitive), we are promulgating this option under the authority
of section 112(d)(6) of the CAA. The control requirements and
compliance requirements under this CAA section 112(d)(6) option are the
exact same requirements we are promulgating under CAA section 112(f)(2)
to address unacceptable risks for process fugitive emissions (described
in section IV.A of this preamble). As described in that section,
facilities must install, operate, and maintain a process fugitives
capture system that is designed to capture 95 percent or more of the
process fugitive emissions. Facilities will also need to meet an
average opacity of 8 percent for each furnace cycle (about 90-120
minutes) with a maximum opacity of no more than 20 percent opacity for
any two consecutive 6-minute block opacity readings (12-minute period).
To demonstrate compliance, facilities will need to initially monitor
opacity for a full furnace cycle (about 90-120 minutes) at least once
per week per furnace building using the DCOT. Moreover, facilities will
need to monitor various control parameters (such as fan speed,
amperage, pressure drops, and/or damper positioning) to ensure the
fugitive capture system and controls are working properly.
Comment: One commenter states that the only notable development
that occurred in ferroalloys emission practices, processes, and control
technologies since the 1999 NESHAP took effect is the installation of
scrubbers and baghouses. Since scrubbers and baghouses have
demonstrably different performance in controlling particulate
emissions, the commenter claims that developments since 1999 warrant
separate particulate emission limits based on the type of control
device involved. The commenter states that the EPA did not acknowledge
this development and proposed a single stack particulate limit for all
furnaces. The commenter provided proposed PM limits of 27 mg/dscm for
wet particulate scrubbers and 6.2 mg/dscm for baghouses, and notes that
these limits would actually reduce the total allowable particulate
emissions from their facility in comparison to the EPA's proposed
single limit of 25 mg/dscm.
Response: Section 112 of the CAA grants the EPA discretion to
establish ``categories and subcategories'' of sources to be regulated
under CAA section 112, and further allows the EPA to ``distinguish
among classes, types and sizes of sources within a category or
subcategory'' when establishing MACT standards. However, we believe it
is not appropriate to establish subcategories based on type of control
technology used by these emission sources.
In the case of the PM emissions from the ferroalloy furnaces, we
believe if it was appropriate, we could subcategorize based on the size
of the furnace or the product being produced in that furnace. However,
we determined that there was no statistical difference in PM emissions
based on the size of the individual furnaces or by the product being
produced in those furnaces. Therefore, we decided it was not
appropriate to subcategorize for PM emissions and instead established a
single PM limit for all of the furnaces, regardless of size or product
being produced.
Comment: One commenter believes that the EPA's proposed
requirements to reduce process fugitive emissions under CAA section
112(d)(6) are not based on control practices in use in the ferroalloys
industry, but rather simply reflect a decision by the EPA that the
sources at Eramet and Felman should be subject to additional
requirements. By putting the enhanced fugitive control requirements
under CAA section 112(d)(6), the commenter believes that the EPA
dispenses with any attempt to justify the requirements as cost
effective, as would be required to impose for ``beyond the MACT floor''
standards under CAA section 112(d)(2), and the EPA dispenses with any
attempt to present a risk-based justification for the requirements, as
would be required under CAA section 112(f)(2).
Response: As an initial matter, we note the process fugitive
control requirements are justified as risk-based requirements under CAA
section 112(f)(2). See section IV.A of this preamble. Therefore, the
premise of this comment is factually incorrect. That said, the
requirements of this rule also are justified under CAA section
112(d)(6). Under CAA section 112(d)(6), we are required to review
emission standards no less frequently than every 8 years and revise
them ``as necessary (taking into account developments in practices,
processes, and control technologies).'' The ferroalloys industry
already includes some of the controls envisioned under this control
scenario. For example, all 5 furnaces in the source category in the
U.S. already have some type of primary hooding to capture some process
fugitive emissions from tapping and/or casting operations. In fact, one
of the five furnaces in the U.S. already achieves good capture of
[[Page 37380]]
tapping emissions with their current configuration. Furthermore,
effective primary and secondary capture systems are currently used in
other metals industries (e.g., steel production, secondary lead
production) to effectively capture and control process fugitives.
Moreover, as described above, representatives from the ferroalloys
companies have provided suggestions as to how such a system could be
designed, installed and operated to achieve 95-percent capture of
fugitives. Therefore, we conclude such a system is technically
feasible. Furthermore, as we described above, we conclude these
controls would be cost effective ($91,000 per ton of HAP metal
reduced). Therefore, we conclude it is appropriate to promulgate this
control option under section 112(d)(6) of the CAA.
4. What is the rationale for our final approach for the technology
review?
a. PM Emissions Limits from Stacks. The available test data from
the five furnaces located at the two facilities indicate that all of
these furnaces have PM emission levels that are well below their
respective emission limits in the 1999 MACT rule. These findings
demonstrate that the add-on emission control technologies (Venturi
scrubber, positive pressure fabric filter, negative pressure fabric
filter) used to control emissions from the furnaces are effective in
reducing particulate matter (used as a surrogate for metal HAP).
The PM emissions, used as a surrogate for metal HAP, that were
reported by the industry in response to the 2010 ICR, were far below
the level specified in the current NESHAP, indicating improvements in
the control of PM emissions since promulgation of the current NESHAP.
We re-evaluated the data received in 2010, along with additional data
received in 2012 and 2013, to determine whether it is appropriate to
promulgate revised emissions limits for PM from the furnace process
vents. More details regarding the available PM data and this re-
evaluation are provided in the Revised Technology Review for the
Ferroalloys Production Source Category for the Supplemental Proposal,
which is available in the docket. Unlike PAH and Hg stack data, we did
not see significant differences in emissions based on product produced
(e.g., FeMn or SiMn). Therefore, we are not promulgating separate PM
stack limits based on product type.
Based on this analysis, we determined it is appropriate to finalize
the revised existing source furnace stack PM emissions limit of 25 mg/
dscm, which is the same limit we proposed in the supplemental proposal.
No additional add-on controls are expected to be required by the
facilities to meet the revised existing source limit of 25 mg/dscm.
However, this revised limit will result in significantly lower
``allowable'' PM emissions from the source category compared to the
level of emissions allowed by the 1999 MACT rule and would help prevent
any emissions increases. To demonstrate compliance, these sources will
be required to conduct periodic performance testing and develop and
operate according to a baghouse operating plan or continuously monitor
Venturi scrubber operating parameters. Also furnace baghouses will be
required to be equipped with BLDS.
The final PM standard for new and reconstructed furnaces is 4.0 mg/
dscm and was determined by evaluating the available data from the best
performing furnace (which was determined to be furnace #2 at Felman).
As described above, the PM emission limit for the local ventilation
control device outlet was re-evaluated for the supplemental proposal
using compliance test data and test data from the 2012 ICR. We did not
receive any additional data since the supplemental proposal for this
source. Using all the available data for the one existing local
ventilation source, we calculated an emissions limit of 4.0 mg/dscm,
which is the exact same limit we proposed in the supplemental proposal.
We conclude that this is still an appropriate emissions limit for this
source. Therefore, we are promulgating this emissions limit of 4.0 mg/
dscm for existing, new, and reconstructed local ventilation control
device emissions sources. In addition, we are promulgating a PM limit
of 3.9 mg/dscm for any new, reconstructed, or existing MOR process, and
a PM limit of 13 mg/dscm for any new, reconstructed, or existing
crushing and screening equipment, which are consistent with what we
proposed in our November 23, 2011, proposal.
Furthermore, as mentioned in section III of this preamble, we are
promulgating a PM limit of 3.9 mg/dscm for any new, reconstructed, or
existing MOR process, and a PM limit of 13 mg/dscm for any new,
reconstructed, or existing crushing and screening equipment.
2. Standards for Process Fugitive Metal HAP Emissions
In the 2011 proposal, we proposed a requirement for sources to
enclose the furnace building, collect fugitive emissions such that the
furnace building is maintained under negative pressure, and duct those
emissions to control devices. As described above, commenters on the
2011 proposal disagreed with our assessment.
Commenters also raised concerns about worker safety and comfort in
designing and operating full enclosure systems. We believe that such
issues can be overcome with proper ventilation design and installation
of air conditioning systems and other steps to ensure these issues are
not a problem. However, after further review and evaluation, we
conclude that it would be quite costly for these facilities to become
fully enclosed with negative pressure and achieve the appropriate
ventilation and conditioning of indoor air.
We re-evaluated the costs and operational feasibility associated
with the full building enclosure with negative pressure. We consulted
with ventilation experts who have worked with hot process fugitives
similar to those found in the ferroalloys industry (e.g., electric arc
furnace steel mini-mills and secondary lead smelters). We determined
that substantially more air flow, air exchanges, ductwork, fans and
control devices and supporting structural improvements would be needed
(compared to what we had estimated in the 2011 proposal) to achieve
negative pressure and also ensure adequate ventilation and air quality
in these large furnace buildings. Therefore, as explained in the
supplemental proposal, we determined that the proposed negative
pressure approach presented in the 2011 proposal would be much more
expensive than what we had estimated in 2011 and may not be feasible
for these facilities.
As mentioned above, for the supplemental proposal, we also
evaluated another option based on enhanced capture of the process
fugitive emissions using a combination of effective local capture with
primary hooding close to the emissions sources and/or secondary capture
of remaining fugitives with roof-line capture hoods and control
devices. These buildings are currently designed such that fugitive
emissions that are not captured by the primary hoods flow upward with a
natural draft to the open roof vents and are vented to the atmosphere
uncontrolled. Under our enhanced control scenario, the primary capture
close to the emissions sources would be significantly improved with
effective local hooding and ventilation and the remaining fugitive
emissions (that are not captured by the primary hoods) would be drawn
up to the roof-line and
[[Page 37381]]
captured with secondary hooding and vented to control devices.
In cases where additional collection of fugitives from the roof
areas is needed to comply with the rule, fume collection areas may be
isolated via baffles (so the area above the furnace where fumes collect
may be kept separated from ``empty'' spaces in large buildings) and
roof openings over fume collection areas can be sealed and fumes
directed to control devices. The fugitive emission capture system
should achieve inflow at the building floor, but outflow toward the
roof where most of the remaining fugitives would be captured by the
secondary hooding. We concluded that a rigorous, systematic examination
of the ventilation requirements throughout the building is the key to
developing a fugitive emission capture system (consisting of primary
hoods, secondary hoods, enclosures, and/or building ventilation ducted
to PM control devices) that can be designed and operated to achieve
very low levels of fugitive emissions. Such an evaluation considers
worker health, safety, and comfort and it is designed to optimize
existing ventilation options (fan capacity and hood design). Thus, we
concluded that an enhanced capture system based on these design
principles does represent an advancement in technology. We estimate
that this type of control system could capture 95 percent of the
process fugitive emissions and vent those emissions to PM control
devices. This enhanced local capture option is described in more detail
in the Revised Technology Review for the Ferroalloys Production Source
Category and in the Cost Impacts of Control Options to Address Fugitive
HAP Emissions for the Ferroalloys Production NESHAP Supplemental
Proposal documents, which are available in the docket.
Under this control option, the cost elements vary by plant and
furnace and include the following:
Curtains or doors surrounding furnace tops to contain
fugitive emissions;
Improvements to hoods collecting tapping emissions;
Upgrade fans to improve the airflow of fabric filters
controlling fugitive emissions;
Addition of ``secondary capture'' or additional hoods to
capture emissions from tapping platforms or crucibles;
Addition of fugitives capture for casting operations;
Improvement of existing control devices or addition of
fabric filters; and
Addition of rooftop ventilation, in which fugitive
emissions escaping local capture are collected in the roof canopy over
process areas through addition of partitions, hoods, and then directed
through ducts to control devices.
We estimate the total capital costs of installing the required
ductwork, fans and control devices under the enhanced capture option
(which is described above and in more detail in the Cost Impacts of
Control Options to Address Fugitive HAP Emissions for the Ferroalloys
Production NESHAP Supplemental Proposal document) to be $40.3 million
and the total annualized cost to be $7.7 million for the two plants.
The total estimated HAP reduction for the enhanced capture option is 77
tpy at a cost per ton of $103,000 ($52 per pound). We also estimate
that this option would achieve PM emission reductions of 229 tpy,
resulting in cost per ton of PM removed of $34,600 per ton and achieve
particulate matter 2.5 microns and less (PM2.5) emission
reductions of 48 tons per year, resulting in a cost per ton of
PM2.5 removal of $165,000 per ton. We believe these controls
for process fugitive HAP emissions (described above), which are based
on enhanced capture (with primary and secondary hooding) are feasible
for the Ferroalloys Production source category from a technical
standpoint and are cost effective. These cost effectivenesses are in
the range of cost effectiveness for PM and HAP metals from other
previous rules. However, it is important to note that there is no
bright line for determining acceptable cost effectiveness for HAP
metals. Each rulemaking is different and various factors must be
considered. Some of the other factors we consider when making decisions
whether to establish standards beyond-the-floor (BTF) under CAA section
112(d)(2) or under CAA section 112(d)(6) include, but are not limited
to, the following: which of the HAP metals are being reduced and by how
much; total capital costs; annual costs; and costs compared to total
revenues (e.g., costs to revenue ratios).
As described in the supplemental proposal, we also re-evaluated the
option based on full building enclosure with negative pressure.
Based on those analyses, we concluded in the supplemental proposal
and conclude again in this action that the full-building enclosure
option with negative pressure may not be feasible and would have
significant economic impacts on the facilities (including potential
closure for one or more facilities). Therefore, we are not promulgating
an option based on full building enclosure with negative pressure.
However, consistent with the supplemental proposal, we conclude
that the enhanced local capture option is a feasible and cost-effective
approach to achieve significant reductions in fugitive HAP emissions
and will achieve almost as much reductions as the full-building
enclosure option (229 vs. 252 tons PM reductions) and, thus, achieving
most of the emission reductions at significantly lower costs. In light
of the technical feasibility and cost effectiveness of the enhanced
capture option, we are promulgating the enhanced capture option under
the authority of section 112(d)(6) of the CAA.
Regarding monitoring requirements, as described above, in the 2011
proposal, we proposed that facilities would need to conduct day-to-day
continuous monitoring of differential pressure to comply with the
proposed full building enclosure with negative pressure requirements.
With the move to the enhanced local capture alternative option,
there is no longer any requirement to monitor negative pressure. Under
this option, the main ongoing compliance requirements will be based on
opacity readings and parametric monitoring. Therefore, since opacity is
a main method of monitoring compliance for process fugitive emissions
controls, we believe that frequent opacity monitoring is necessary, as
reflected in the supplemental proposal. Furthermore, as we explained in
the supplemental proposal, we believe an average opacity limit of 8
percent is appropriate to ensure effective capture and control of
process fugitive emissions over the entire furnace cycles and that a
maximum opacity of 20 percent for any 2 consecutive 6-minute periods is
appropriate to prevent spikes in fugitive emissions. Therefore, we are
promulgating an average opacity limit of 8 percent and a maximum
opacity limit of 20 percent for any 2 consecutive 6-minute periods.
Regarding opacity monitoring, we are promulgating a requirement
that facilities conduct opacity observations at least once per week for
a full furnace cycle for each operating furnace and each MOR operation
using the DCOT instead of Method 9. We believe the DCOT is appropriate
for the final rule because it provides more objective and better
substantiated opacity readings. However, as described above, we are
allowing an opportunity for facilities to decrease frequency of opacity
monitoring to monthly after 26 compliant weekly readings.
Similar to the supplemental proposal, we are also finalizing the
requirement
[[Page 37382]]
that, if the average opacity reading from the shop building is greater
than 8-percent opacity during an observed furnace process cycle, an
additional two more furnace process cycles must be observed such that
the average opacity during the entire observation period is less than
7-percent opacity. A furnace process cycle means the period in which
the furnace is tapped to the time in which the furnace is tapped again
and includes periods of charging, smelting, tapping, casting, and ladle
raking.
As mentioned above, we are also promulgating the requirement that
at no time during operation may any two consecutive 6-minute block
opacity readings be greater than 20-percent opacity.
We believe that the source should demonstrate that the overall
design of the ventilation system is adequate to achieve the final
standards. Therefore, we are promulgating the requirement that
facilities in this source category must install, operate, and maintain
a process fugitives capture system that is designed to collect 95
percent or more of the process fugitive emissions from furnace
operations, casting MOR process, ladle raking and slag skimming and
crushing, and screening operations, and convey the collected emissions
to a control device that meets specified emission limits and the
opacity limits. We are also requiring continuous monitoring of key
ventilation operating system parameters and periodic inspections of the
ventilation systems to ensure that the ventilation systems are
operating as designed.
We believe that if the facilities design the capture and control
systems according to the most recent (at the time of construction)
ventilation design principles recommended by the American Conference of
Governmental Industrial Hygienists (ACGIH), including detailed
schematics of the ventilation system design, addressing variables that
affect capture efficiency such as cross drafts and describes protocol
or design characteristics to minimize such events and identifies
monitoring and maintenance steps, the plan will be capable of ensuring
the system is properly designed and continues to operate as designed.
Therefore, we are promulgating the requirement that facilities develop
such a plan and submit this plan to the permitting authority. The plan
must also be incorporated into the source's operating permit and
updated every 5 years or when there is a significant change in
variables that affect process fugitive emissions ventilation design.
This design plan, coupled with the requirement for frequent opacity
observations and operating parameter monitoring, will ensure fugitive
emissions are effectively controlled and will result in enforceable
requirements. We recognize that other design requirements and/or more
frequent opacity observations may yield more compliance certainty, but
incur greater costs and not result in measurable decreases in
emissions.
We believe the additional PM data we received justifies the revised
PM stack emission limits we are promulgating under the authority of
section 112(d)(6) of the CAA. We also believe the enhanced capture and
control is a development in technology that is feasible and cost
effective, so we are promulgating the enhanced local capture and
control option under the authority of section 112(d)(6) of the CAA.
Furthermore, we believe it is appropriate to promulgate the DCOT to
ensure adequate furnace capture and control.
C. CAA Section 112(d)(2) & (3) Revisions for the Ferroalloys Production
Source Category
1. What did we propose pursuant to CAA section 112(d)(2) & (3) for the
Ferroalloys Production source category?
In the November 23, 2011, proposal, we proposed a formaldehyde
emission limit of 201 [mu]g/dscm for any new, reconstructed, or
existing electric arc furnace.
In the October 6, 2014, supplemental proposal, we proposed the
following:
HCL emission limit of 180 [mu]g/dscm for new or
reconstructed electric arc furnaces and 1,100 [mu]g/dscm for existing
electric arc furnaces;
Hg emission limit of 17 [mu]g/dscm for new or
reconstructed electric arc furnaces producing FeMn, and 170 [mu]g/dscm
for existing electric arc furnaces producing FeMn;
Hg emission limit of 4 [mu]g/dscm for new or reconstructed
electric arc furnaces producing SiMn and 12 [mu]g/dscm for existing
electric arc furnaces producing SiMn;
PAH emission limit of 880 mu;g/dscm for new or
reconstructed electric arc furnaces producing FeMn and 1,400 [mu]g/dscm
for existing electric arc furnaces producing FeMn; and
PAH emission limit of 72 [mu]g/dscm for new or
reconstructed electric arc furnaces producing SiMn and 120 [mu]g/dscm
for existing electric arc furnaces producing SiMn.
2. How did the CAA section 112(d)(2) & (3) revisions change for the
Ferroalloys Production source category?
In mid-August 2014, a few weeks prior to the signature of the
supplemental proposal, we received a test report with Hg and PAH data,
which we were unable to incorporate into the proposed limits in the
supplemental proposal, in part because of the timing and in part
because we had not completed our review and technical analysis of the
data. We noted receipt of the data and invited comment on it in the
supplemental proposal, and made the data available for review. We
committed to considering these data in the final rule based on public
comment and our technical analysis. In addition to the pre-supplemental
proposal data, another Hg and PAH test report was received during the
comment period. The new test data for FeMn production received in
August 2014 and during the comment period had much higher PAH
concentrations than the data that were previously provided. The new PAH
test data for SiMn production were only slightly higher than previous
data received from the facilities. The new Hg data for both FeMn and
SiMn production were comparable to the test data that we used to
develop the proposed limits for the supplemental proposal.
For this action, we re-evaluated the PAH and Hg emission limits to
include the new test data. The 99-percent upper prediction limit (UPL)
calculation using all the available reliable data for PAH emissions
results in an emissions limit of 12,000 [mu]g/dscm for existing
furnaces producing FeMn and 130 [mu]g/dscm for existing furnaces
producing SiMn.
With regard to new source limits, as mentioned previously, there
are only two furnaces in the source category that produce FeMn, and
both furnaces are located at Eramet. The units are similar in design
and process the same types of raw materials, and we, therefore, expect
little or no difference in the performance of these units. The
available emissions data, which show that the two units mean emissions
are only 2-percent different, support this hypothesis. We conclude,
based on the similarities in the units and the available data, that
these two furnaces achieve the same degree of control of PAH emissions
with their current control devices. Accordingly, we consider these two
units to be equal performers with regard to PAH emissions and
therefore, we used all the data from both units to calculate the new
source emissions limit. Using the 99-percent UPL calculation, we derive
[[Page 37383]]
an emissions limit of 11,500 [mu]g/dscm for new furnaces producing
FeMn.
For SiMn, there were no changes to the best performing source and
the PAH limit of 72 [mu]g/dscm proposed in the supplemental proposal is
the same limit selected for the final rule for new furnaces producing
SiMn.
The 99-percent UPL for PAHs for FeMn production is about 8 times
higher than the proposed PAH limit for FeMn in the supplemental
proposal, whereas the 99-percent UPL for PAHs for SiMn production is
comparable to the proposed limit in the supplemental proposal. The new
data show there is substantial variability in PAH emissions from the
furnaces, especially during FeMn production.
As mentioned in section III.E of this preamble, due to the large
variation in PAH emissions from furnace stacks during FeMn production,
we are requiring quarterly compliance tests for PAHs (i.e., four PAH
compliance tests per year) for furnaces while producing FeMn, with an
opportunity for facilities to apply for decreased frequency of such
compliance testing from their permit authority after the first year and
after four or more successful PAH compliance tests have been completed
and submitted to the permit authority.
We expect that any application submitted by an affected source to
request reduced frequent compliance testing for PAHs should include
information regarding the four or more compliant test results and what
factors or conditions are contributing to the quantity and variation of
PAH emissions. For example, the application could include, among other
things, information about the amounts and types of input materials,
types of electrodes used, electrode consumption rates, furnace
temperature and other furnace, process or product information that may
be affecting the PAH emissions.
The re-evaluation of the Hg test data, which includes the new test
data, produced a 99-percent UPL of 130 [mu]g/dscm for existing furnaces
producing FeMn and 12 [mu]g/dscm for existing furnaces producing SiMn.
For new sources, the new test data did not affect the 99-percent UPL of
4 [mu]g/dscm for new furnaces producing SiMn.
With regard to the new source limit in the supplemental proposal
for Hg for furnaces producing FeMn, the proposed new source limit was
based on BTF controls using activated carbon injection (ACI), and
assuming 90-percent reduction. We continue to conclude that it is
appropriate to require BTF controls for new FeMn sources consistent
with the supplemental proposal (assuming 90-percent reduction).
Therefore, we calculate that the new source limit for the final rule
for Hg for furnaces producing FeMn will be 13 [mu] g/dscm (i.e., 130
[mu] g/dscm minus 90-percent control). These UPL values are generally
consistent with, but a bit lower than, the proposed limits in the
supplemental proposal.
3. What key comments did we receive on the CAA section 112(d)(2) & (3)
proposed revisions, and what are our responses?
Several comments were received regarding the CAA section 112(d)(2)
& (3) proposed revisions for the Ferroalloys Production source
category. The following is a summary of these comments and our
responses. Other comments received and our responses can be found in
the document titled National Emission Standards for Hazardous Air
Pollutant Emissions: Ferroalloys Production Summary of Public Comments
and the EPA's Responses on Proposed Rule (76 FR 72508, November 23,
2011) and Supplemental Proposal (79 FR 60238, October 6, 2014), which
is available in the docket for this action (EPA-HQ-OAR-2010-0895).
Comment: Commenters claimed the EPA was establishing MACT floors
for the newly regulated HAP based on limited data. The commenters noted
that for many of these pollutants, there is limited understanding of
the mechanism of their generation in the process and the variability in
the level of their occurrence. As a result, it is essential that EPA
use all reasonably available data in establishing these standards.
The commenters noted the EPA excluded PAH data for both SiMn and
FeMn production, that showed higher levels of emissions. They believe
the exclusion of these data led to calculation of a proposed MACT floor
for PAH that is below the level that can be demonstrably achieved by
the best performing sources.
The commenters argued that the EPA should reconsider its decision
not to include these data in calculation of the MACT floor. One
commenter noted that additional testing to better characterize
variability, particularly for PAH, was being performed prior to the
comment period for the supplemental proposal and encouraged the EPA to
consider these additional data in calculating the MACT floor levels for
the final standard.
Response: We have received multiple test reports from the industry
during the development of the supplemental proposal and during the
comment period for the supplemental proposal. Each test report received
was reviewed to determine if the test met the quality assurance/quality
control (QA/QC) requirements for this RTR. Only test data that met
these requirements were used to estimate emissions used for determining
residual risk from the emissions sources and for determining the MACT
floor limits. Most data we received passed the QA/QC process and were
judged to be valid data and were used in our risk analyses and MACT
floor calculations, including data received shortly before publication
of the supplemental proposal and data received during the comment
period. The final rule MACT floor limits include the updated data.
However, a few tests we received previously did not meet the QA/QC
requirements and, therefore, were not used in these analyses. For
further explanation of the data evaluation, see the Revised Development
of the Risk and Technology Review (RTR) Emissions Dataset for the
Ferroalloys Production Source Category for the 2015 Final Rule
document, which is available in the docket.
Even though some of the test data received did not meet the QA/QC
requirements for this RTR, we believe we still have a robust set of
test data for most of the HAP and the majority of the MACT floor
analyses are based on multiple tests from each of the facilities.
Comment: One commenter believes the EPA has not demonstrated that
ACI on new furnaces will provide any benefits. The commenter notes that
the EPA estimated that Eramet emits only an estimated 274 pounds of Hg
per year, and Hg emissions do not contribute to multipathway exposures
exceeding an HQ of 1. Thus, reducing Hg emissions would not address any
existing risks.
If no added cost was involved, lowering Hg emissions might be a
worthwhile objective. But, the fact is that cost is a relevant concern
under CAA section 112(d)(2) and, as discussed below, achieving the
proposed new source standards would be prohibitively expensive.
The commenter states that the EPA justifies its conclusion that ACI
is affordable for new sources based on the assumption that any new
source will be built with a baghouse. As a threshold matter, the EPA's
assertion that ACI is cost effective when applied to baghouse-
controlled sources is contradicted by its own supporting memorandum.
According to Table 6-3 of the Memorandum from Bradley Nelson, EC/R,
Inc. to Phil Mulrine, EPA OAQPS/SPPD/MICG on Mercury Control Options
and Impacts for the Ferroalloys Production Industry (Aug. 29, 2014),
[[Page 37384]]
adding ACI is 5 times more expensive to add to a baghouse than to a
scrubber, and operational costs are 3 times higher. The table, thus,
indicates that the cost per pound of Hg removed would be higher, not
lower, for EMI's baghouse-controlled source, and EPA's estimated
marginal cost is $22,195 per pound, almost twice the cost presented by
the EPA in the preamble to the 2014 proposal. Since this is based on an
unrealistic removal rate, the unit cost would actually be at least
$44,000 per pound of Hg removed.
Second, the commenter states that the sole economic justification
for ACI is the EPA's substantially understated unit cost of $17,600 for
each pound of Hg removed. The EPA's cost-per-pound metric is completely
untethered to any cost-benefit analysis. To say how much it will cost
to remove a pound of Hg provides no practical basis for assessing the
relative value of removing that pound of Hg or the relative ability of
a ferroalloys producer to absorb that cost. The docket contains no
demonstration, much less substantial evidence, that the lower cost
would nevertheless be affordable by EMI.
Finally, the commenter notes that the facility is captive to the
pricing structure imposed by low-cost foreign ferroalloy producers who
will not be subject to the requirements of this rule. Accordingly,
foreign producers prevent the facility from passing on costs such as
this to customers via higher prices. Before that facility can construct
a new furnace, it would have to determine that the new furnace would
produce a positive return large enough to cover the cost of
constructing and operating that additional furnace, while charging the
same price charged by producers not incurring the added costs of ACI.
The EPA provides no explanation for why it believes this would be
possible and our analysis strongly suggests that it would not be
possible.
The commenter states that the net result is that the proposed new
source standard effectively prevents EMI from increasing FeMn
production in the future via a new furnace and ensures that when the
existing furnaces require replacement, they will not be replaced with
furnaces capable of producing FeMn. The EPA's proposed new source
standard is inconsistent with EPA's recognition in the 2014 proposal
that EMI is the sole U.S. source of FeMn for domestic steel production,
and its judgment that ACI should not be immediately required, in part,
because such a requirement would likely force EMI out of business. The
proposed Hg ``beyond-the-MACT-floor standard'' produces the same result
that the EPA agrees should be avoided, only at a later date.
Response: Activated carbon injection in conjunction with fabric
filter technology has been successfully used to reduce emissions of Hg
from a number of different industries. In addition, the use of
brominated carbon has been used to oxidize the Hg allowing even greater
control effectiveness for Hg.
The determination of the Hg limits for new or major reconstructed
furnaces is based on the assurance that such sources would be
constructed to include a baghouse as the primary PM control device (in
order to comply with the proposed lower new source limits for PM) and
then they could add ACI after the baghouse for Hg control along with a
polishing baghouse and would achieve at least 90-percent reduction of
Hg.
In the supplemental proposal, the estimated costs for beyond the
floor controls for mercury for new and reconstructed sources were based
on the costs of installing and operating brominated ACI and a polishing
baghouse. Based on this, in the supplemental proposal, we estimated
that the cost effectiveness of BTF controls for a new and major
reconstructed FeMn production source would be about $12,000/lb. This
cost effectiveness estimate is well within the range of cost
effectiveness levels we have decided were reasonable in other rules.
Furthermore, no other significant economic factors were identified that
would indicate that these limits would be inappropriate or infeasible
for new sources. Therefore, in the supplemental proposal, we concluded
that BTF controls would be cost-effective and feasible for any new or
major reconstructed furnace that produces FeMn.
We received new Hg test data prior to and during the comment period
for the supplemental proposal. Using these new test data along with the
previous data we re-evaluated the cost of installing ACI to reduce Hg.
Similar to the supplemental proposal, we estimated costs for BTF
controls for Hg for new and reconstructed sources based on the costs of
installing and operating brominated ACI and a polishing baghouse. Based
on this re-evaluation, we estimate that the cost effectiveness of
installing ACI for a new and major reconstructed FeMn production source
would be about $13,600/lb for a furnace producing FeMn 50 percent of
the year, and $7,100/lb for a furnace producing FeMn 100 percent of the
year.
These cost effectiveness estimates are similar to the estimate we
presented in the supplemental proposal for the beyond the floor option
for new FeMn furnaces and continue to be within the range of cost
effectivenesses we have determined are reasonable for mercury control
in other rulemakings. Furthermore, no other significant economic
factors were identified that would indicate these limits would be
inappropriate or infeasible for new or major reconstructed furnaces
that produce FeMn. Therefore, we believe the BTF control option for Hg
emissions is economically and technically feasible for new and major
reconstructed FeMn furnaces and that these cost effectivenesses are
acceptable for any new or major reconstructed furnace that produces
FeMn. Additional discussion of the EPA's BTF analyses for mercury are
available in the Final Rule Mercury Control Options and Impacts for the
Ferroalloys Production Industry document and in the Mercury Control
Options and Impacts for the Ferroalloys Production Industry document
(dated August 2014) that EPA published in support of the 2014
supplemental proposal. These documents are available in the docket for
this action.
An assessment of the cost effectiveness of emission reductions,
along with other economic factors, is an appropriate method for
assessing cost impacts in standard setting when CAA section 112 allows
cost to be a factor in EPA's decision-making. Nothing in CAA section
112 compels EPA to use cost-benefit analysis in standard-setting
decisions. Moreover, to the extent the commenter bases its position
that the new source BTF standard for mercury lacks benefits because it
does not address ``any existing risk,'' the court of appeals has held
that risk is not a consideration when setting MACT standards, as in
Sierra Club v. EPA, 353 F.3d 976, 981 (D.C. Cir. 2004). The emission
standards in this rule discharge EPA's CAA section 112(d)(2) duties
with respect to Hg emissions from new and existing electric arc
furnaces in this source category.
4. What is the rationale for our final approach for the CAA section
112(d)(2) and (3) revisions?
We evaluated and rejected BTF options for the CAA section 112(d)(2)
and (3) revisions in the supplemental proposal and proposed MACT floor
emissions limits for formaldehyde, HCl, Hg, and PAH for existing
sources. We also evaluated and rejected BTF options for new sources for
formaldehyde, HCl, and PAHs. For Hg, we also evaluated BTF options for
new furnaces. We rejected BTF for new SiMn furnaces. However, we
proposed BTF limits for Hg for FeMn furnaces. See the Revised
[[Page 37385]]
MACT Floor Analysis for the Ferroalloys Production Source Category
document and the Final Rule Mercury Control Options and Impacts for the
Ferroalloys Production Industry document, which are available in the
docket.
We are promulgating MACT floor-based limits for the four HAP
described above for existing sources under CAA section 112(d)(2) and
(3) as described above, which is the same approach as in the
supplemental proposal. Regarding new sources, we are promulgating MACT
floor limits for new sources for formaldehyde, HCl, and PAHs, and for
Hg for new SiMn furnaces. However, we are promulgating a BTF limit for
Hg for FeMn furnaces.
The limits for HCl and formaldehyde are exactly the same as
proposed. The Hg limits for FeMn and SiMn production and PAH limits for
SiMn production changed slightly due to the inclusion of additional
data. The only significant change was for the PAH limit for FeMn
production, which is about 8 times higher than what we proposed. In our
supplemental proposal, we provided notice of receipt of the highest
test data (i.e., the data received in August 2014) which when combined
with the other data resulted in a higher PAH limit. While these data
had not been completely QA/QCed before the supplemental proposal, both
the method for calculating a limit and most of the data on which the
final limit was calculated were available and addressed in the
supplemental proposal. Furthermore, commenters agreed that the final
limit should be based on all available valid data. As we stated
previously, any changes to the Hg and PAH emissions limits were a
result of using all of the available valid data which resulted in a
change to the MACT floor calculations. Additional data received during
the comment period confirmed a higher PAH limit was justified.
D. What changes did we make to the Ferroalloys Production opacity
monitoring requirement?
1. What changes did we propose for the ferroalloys production opacity
monitoring requirement?
In the 2014 supplemental proposal, the EPA solicited comment
regarding the use of new technologies to provide continuous or near
continuous long term approaches to monitoring emissions from industrial
sources such as the ferroalloys production facilities within this
source category. Specifically, we were seeking comment on the
feasibility and practice associated with the use of automated opacity
monitoring with ASTM D7520-13, using DCOT at fixed points to interpret
visible emissions from roof vents associated with the processes at each
facility, and how this technology could potentially be included as part
of the requirements in the NESHAP for ferroalloys production sources.
2. How did the opacity monitoring requirements change for the
Ferroalloys Production source category?
Based on the information we received during the comment period for
the supplemental proposal and after further evaluation of the
technology, we believe that the use of DCOT can provide opacity
readings comparable to Method 9 and reduce the burden of requiring a
person to conduct opacity readings over the furnace cycle. Furthermore,
the DCOT provides objective and well-substantiated readings of opacity.
The DCOT camera provides an image that the facility could access
immediately, with QA/QC done within 45 minutes to validate the image
and initial readings. In comparison, it would take a field observer
roughly 30 minutes to return from the field and average their manually
assembled data such that they can report the average that they recorded
over the previous 90 minutes of observations. We view the initial
visible recording as sufficient evidence to provide the facility enough
reason to initiate, investigate, and correct concerns that may create
elevated visual emissions observations, and the 45-minute turnaround
time on actual opacity values to be quick enough to provide a facility
the confirmation they would need to be assured that they have taken
appropriate action.
3. What key comments did we receive on the opacity monitoring
requirement, and what are our responses?
Comment: In their supplemental proposal comments, one commenter
objects to the significantly increased frequency of opacity
observations from once every 5 years to weekly. They note that the
Agency states that the frequency is ``appropriate'' to demonstrate
compliance with the process fugitive standard with the enhanced
frequency presumably substituting for the continuous negative pressure
monitoring obligations from the 2011 proposal.
The commenter believes that this explanation overlooks the
stringent continuous monitoring that the proposed rule already requires
to ensure that the process fugitives control system meets the 95-
percent capture requirement. First, the facility must develop a plan to
demonstrate 95-percent capture, and that plan must be approved by the
permitting authority. Next, the facility must perform an initial
compliance demonstration. The facility must then identify specific
parameters, either through the engineering assessment or the initial
compliance demonstration, that are indicative of compliance with the
opacity standard. Finally, on an ongoing basis, the facility must
routinely monitor those parameters.
The commenter notes that an initial compliance demonstration and
ongoing monitoring is a standard regulatory approach required in any
number of MACT standards. However, none of these other standards
require weekly testing to confirm that the parameters and limits are
still being met and many other standards require re-testing only every
5 years, or at most annually. They believe that nothing in the current
proposal demonstrates why it is necessary or appropriate to deviate
from this standard approach here.
Two commenters believe that the proposed weekly opacity testing
will impose significant ongoing costs on the facilities for no
additional environmental benefit. They believe that the ongoing
parametric monitoring is sufficient to ensure compliance on an ongoing
basis.
These commenters believe that the weekly opacity reading
requirement is overly burdensome, especially for Eramet because they
have three shop buildings. They estimate 3-5 hours per building opacity
reading for a total of 9-15 hours a week for reading opacity.
Response: We re-evaluated the opacity monitoring requirements in
the supplemental proposal and determined that the DCOT and ASTM D7520-
13 provided a development that ensures compliance with the fugitive
emissions standards, as well as reduces the labor burden on the
facilities. After initial setup, the DCOT can measure the opacity
during the furnace process cycle without any labor needed. In addition,
facilities would not have the cost of annual certification as is the
case with Method 9. We estimate that the overall costs of DCOT and ASTM
D7520-13 will be approximately the same as what the overall costs would
be if facilities used method 9. In addition, due to the baseline
unacceptable risk finding being based largely on process fugitive
manganese emissions, we believe the frequent opacity readings using the
objective and substantiated results of DCOT are warranted to ensure
fugitive emissions are effectively captured and controlled. However,
after considering comments, we decided to allow facilities an
opportunity to reduce the
[[Page 37386]]
frequency of opacity readings to once per month per furnace building
(instead of weekly) if the facility achieves 26 consecutive compliant
weekly readings for that furnace building. This reduction in frequency
will reduce the cost burden for the facilities. However, if any of the
subsequent monthly readings exceed the opacity limit for that furnace
building, the facility must return to weekly readings until they
achieve another 26 compliant weekly readings, at which time the
facility can return to monthly readings.
Comment: One commenter supported the EPA's determination that
opacity observations should be measured over a furnace process cycle.
However, because all furnaces at the Felman facility are located in the
same building, the commenter suggests treating the building as a single
opacity source, and that opacity observations be conducted over a time
period that captures a full furnace process cycle from each furnace
within that building.
Response: We agree with the commenter and have revised the opacity
requirements to include opacity determinations from buildings with
multiple furnaces. The requirement will treat the building with
multiple furnaces as a single opacity source and the opacity readings
will be conducted over a time period that will include tapping from
each of the furnaces in operation.
Comment: In comments on the supplemental proposal, two commenters
state that the EPA should require the use of the best available testing
method, digital opacity monitoring. The commenters describe the
benefits of the DCOT compared to Method 9 and provide supporting
documentation. In particular, one commenter supports the DCOT because
it is EPA certified as a valid test method for opacity and approved for
its use, the use of a camera creates a good electronic record of the
observations, conditions, location, etc., and a number of regulated
entities are using this method to assess opacity. The commenter adds
that using cameras can save resources, citing a Department of Defense
project to reduce Method 9 certification costs. The commenter adds that
the EPA should also require opacity determinations to be documented on
an electronic form and provided on the Internet in real time for public
review.
One commenter adds that the EPA should not allow Method 9 to be
used, unless there is a power outage requiring the facility to use
Method 9 to assure opacity standard compliance. They also add that
instead of Method 9, the EPA should require a source to use either
continuous opacity monitor or DCOT.
Response: We evaluated the use of DCOT and the ASTM D7520-13 method
and determined that this technology provides the same compliance
assurance as Method 9 measurements with approximately the same overall
burden on the facilities and the DCOT provides reliable, unbiased
opacity readings. Therefore, we are requiring opacity determinations to
be made using DCOT and ASTM D7520-13. With regard to the comment
suggesting that the DCOT results be documented in an electronic format
and provided on the internet in real time, the DCOT results will be
recorded in an electronic format. Furthermore, use of the DCOT will
improve transparency of opacity monitoring results. However, we do not
have a system established to provide these results on the internet in
real time. Furthermore, the ERT is not yet configured to be able to
accept the DCOT compliance images. Nevertheless, the rule requires the
affected sources to maintain electronic records of the DCOT results and
submit periodic compliance monitoring reports to the Administrator or
permit authority. We believe that the public will be able to obtain
copies of the compliance results within a reasonable amount of time by
contacting the EPA and/or the permit authority through the appropriate
channels.
Comment: One commenter requests a clarification to the proposed
regulatory language: That EPA add the phrase ``over a furnace process
cycle'' at the end of 40 CFR 63.1623(b)(3). As written in the
supplemental proposal, the language requires that opacity emissions not
exceed 8 percent, but no averaging time is specified. The proposed
subsections, Sec. 63.1623(b)(3)(i) though (iii) stated that the
compliance demonstration for this obligation must be determined over
the course of an entire furnace process cycle, but they do not clearly
state that the limit itself is 8 percent over the entire furnace
process cycle, and not, for example, an instantaneous limit, or 8
percent over a 6-minute period. To avoid misunderstanding, this
averaging period should be stated clearly as part of the standard
itself.
Response: We agree with the commenter and have included language
that clarifies the opacity requirement in the final rule.
4. What is the rationale for our final decision for the opacity
monitoring requirement?
We are finalizing requirements to measure opacity from the furnace
buildings using ASTM D7520-13 and digital camera technology because we
conclude this is the best method to ensure reliable and unbiased
readings for opacity. We are also finalizing the requirement that
facilities need to meet an average opacity standard of no more than 8-
percent opacity for each furnace cycle. Furthermore, we are finalizing
the requirement that at no time during operation may any two
consecutive 6-minute block opacity readings (12-minute period) be
greater than 20-percent opacity.
V. Summary of Cost, Environmental, and Economic Impacts and Additional
Analyses Conducted
A. What are the affected facilities?
Eramet Marietta Incorporated, in Marietta, Ohio and Felman
Production LLC, in Letart West Virginia, are the 2 manganese
ferroalloys production facilities currently operating in the United
States that will be affected by these amendments. We do not know of any
new facilities that are expected to be constructed in the foreseeable
future. However, there is one other facility that has a permit to
produce FeMn or SiMn in an electric arc furnace, but it is not doing so
at present. It is possible, however, that this facility could resume
production or another non-manganese ferroalloy producer could decide to
commence production of FeMn or SiMn. Given this uncertainty, our impact
analysis is focused on the two existing sources that are currently
operating.
B. What are the air quality impacts?
As noted in the 2011 proposal, emissions of metal HAP from
ferroalloys production sources have declined in recent years, primarily
as the result of state actions and also due to the industry's own
initiative. The final amendments in this rule would cut HAP emissions
(primarily particulate metal HAP such as manganese, arsenic, and
nickel) by about 60 percent from their current levels. Under the final
emissions standards for process fugitives emissions from the furnace
building, we estimate that the HAP emissions reductions would be 77
tpy, including significant reductions of manganese.
C. What are the cost impacts?
Under the revised final amendments, each ferroalloys production
facility is expected to incur costs for the design, installation and
operation of an enhanced local capture system. Each facility also is
expected to incur costs associated with the installation of additional
control devices to manage the air flows generated by the enhanced
[[Page 37387]]
capture systems. There would also be capital costs associated with
installing new or improved continuous monitoring systems, including
installation of BLDS on the furnace baghouses that are not currently
equipped with these systems and installation and operation of DCOT
systems to monitor opacity.
The revised capital costs for each facility were estimated based on
the projected number and types of upgrades required. The specific
enhancements for each facility were selected for cost estimation based
on estimates directly provided by the facilities based on their
engineering analyses and discussions with the EPA. The Cost Impacts of
Control Options to Address Fugitive HAP Emissions for the Ferroalloys
Production NESHAP Supplemental Proposal document includes a complete
description of the revised cost estimate methods used for this analysis
and is available in the docket.
Cost elements vary by plant and furnace and include the following
elements:
Curtains or doors surrounding furnace tops to contain
fugitive emissions;
Improvements to hoods collecting tapping emissions;
Upgraded fans to improve the airflow of fabric filters
controlling fugitive emissions;
Addition of ``secondary capture'' or additional hoods to
capture emissions from tapping platforms or crucibles;
Addition of fugitives capture for casting operations;
Improvement of existing control devices or addition of
fabric filters; and
Addition of rooftop ventilation, in which fugitive
emissions escaping local control are collected in the roof canopy over
process areas through addition of partitions and hoods, then directed
through roof vents and ducts to control devices.
For purposes of the analysis for the final rule, we assumed that
enhanced capture systems and roofline ventilation will be installed for
all operational furnaces at both facilities and for MOR operations at
Eramet Marietta. The specific elements of the capture and control
systems selected for each facility are based on information supplied by
the facilities incorporating their best estimates of the improvements
to fugitive emission capture and control they would implement to
achieve the standards included in the final rule. We estimate the total
capital costs of installing the required ductwork, fans, control
devices, and monitoring to comply with the enhanced capture system
requirements to be $40.3 million and the total annualized cost to be
$7.7 million (2012 dollars) for the two plants. We estimate that
enhanced capture and control systems required by this rule will reduce
metal HAP emissions by 75 tons, resulting in a cost per ton of metal
HAP removed to be $106,000 per ton ($53 per pound). The total HAP
reduction for the enhanced capture and control systems is estimated to
be 77 tpy at a cost per ton of $103,000 per ton ($52 per pound). We
also estimate that these systems will achieve PM emission reductions of
229 tpy, resulting in cost per ton of PM removed of $34,600 per ton and
achieve PM2.5 emission reductions of 48 tpy, resulting in a
cost per ton of PM2.5 removal of $165,000 per ton.
D. What are the economic impacts?
As a result of the requirements in this final rule, we estimate
that the total capital cost for the Eramet facility will be about $25.4
million and the total annualized costs will be about $5.6 million (in
2012 dollars). For impacts to Felman Production LLC, this facility is
estimated to incur a total capital cost of $14.9 million and a total
annualized costs of just under $2.1 million (in 2012 dollars). In
total, these costs could lead to an increase in annualized cost of
about 1.9 percent of sales, which serves as an estimate for the
increase in product prices, and a decrease in output of as much as 10.1
percent. For more information regarding economic impacts, please refer
to the Economic Impact Analysis report and the summary of public
comments and EPA's responses document which are included in the public
docket for this final rule.
E. What are the benefits?
The estimated reductions in HAP emissions (i.e., about 77 tpy) that
will be achieved by this action will provide significant benefits to
public health. For example, there will be a significant reduction in
emissions of HAP metals (especially manganese, arsenic, nickel,
chromium, cadmium, and lead). The rule will also achieve some
reductions of Hg and PAHs. In addition to the HAP reductions, we also
estimate that this final rule will reduce 48 tons in PM2.5
emissions as a co-benefit of the HAP reductions annually.
This rulemaking is not an ``economically significant regulatory
action'' under Executive Order 12866 because it is not likely to have
an annual effect on the economy of $100 million or more. Therefore, we
have not conducted a Regulatory Impact Analysis (RIA) for this
rulemaking or a benefits analysis. While we expect that these avoided
emissions will result in improvements in air quality and reduce health
effects associated with exposure to HAP associated with these
emissions, we have not quantified or monetized the benefits of reducing
these emissions for this rulemaking. This does not imply that there are
no benefits associated with these emission reductions. In fact, our
demographic analysis indicates that thousands of people live within 50
kilometers of these two facilities and these people will experience
benefits because of the reduced exposure to air toxics due to this
rulemaking.
When determining if the benefits of an action exceed its costs,
Executive Orders 12866 and 13563 direct the Agency to consider
qualitative benefits that are difficult to quantify but essential to
consider. Controls installed to reduce HAP would also reduce ambient
concentrations of PM2.5 as a co-benefit. Reducing exposure
to PM2.5 is associated with significant human health
benefits, including avoided premature mortality and morbidity from
cardiovascular and respiratory illnesses. Researchers have associated
PM2.5 exposure with adverse health effects in numerous
toxicological, clinical and epidemiological studies (U.S. EPA,
2009).\4\ When adequate data and resources are available and an RIA is
required, the EPA generally quantifies several health effects
associated with exposure to PM2.5 (U.S. EPA, 2012).\5\ These
health effects include premature mortality for adults and infants,
cardiovascular morbidities such as heart attacks, hospital admissions
and respiratory morbidities such as asthma attacks, acute bronchitis,
hospital and emergency department visits, work loss days, restricted
activity days, and respiratory symptoms. The scientific literature also
suggests that exposure to PM2.5 is also associated with
adverse effects on birth weight, pre-term births, pulmonary function
and other cardiovascular and respiratory effects (U.S. EPA, 2009), but
the EPA has not quantified certain outcomes of these impacts in its
benefits analyses. PM2.5 also increases light extinction,
which is
[[Page 37388]]
an important aspect of reduced visibility.
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\4\ U.S. Environmental Protection Agency (U.S. EPA). 2009.
Integrated Science Assessment for Particulate Matter (Final Report).
EPA-600-R-08-139F. National Center for Environmental Assessment--RTP
Division. Available on the Internet at https://cfpub.epa.gov/ncea/cfm/recordisplay.cfm?deid=216546.
\5\ U.S. Environmental Protection Agency (U.S. EPA). 2012.
Regulatory Impact Analysis for the Proposed Revisions to the
National Ambient Air Quality Standards for Particulate Matter.
Office of Air and Radiation, Research Triangle Park, NC. Available
on the Internet at https://www.epa.gov/ttnecas1/regdata/RIAs/PMRIACombinedFile_Bookmarked.pdf.
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The rulemaking is also anticipated to reduce emissions of other
HAP, including metal HAP (arsenic, cadmium, chromium (both total and
hexavalent), lead compounds, manganese, and nickel) and PAHs. Some of
these HAP are carcinogenic (e.g., arsenic, PAHs) and some are toxic and
have effects other than cancer (e.g., kidney disease from cadmium,
respiratory, and immunological effects from nickel). While we cannot
quantitatively estimate the benefits achieved by reducing emissions of
these HAP, qualitative benefits are expected as a result of reducing
exposures to these HAP. More information about the health effects of
these HAP can be found on the IRIS,\6\ ATSDR,\7\ and California EPA \8\
Web pages.
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\6\ U.S. EPA, 2006. Integrated Risk Information System. https://www.epa.gov/iris/.
\7\ U.S. Agency for Toxic Substances and Disease Registry, 2006.
Minimum Risk Levels (MRLs) for Hazardous Substances. https://www.atsdr.cdc.gov/mrls/.
\8\ CA Office of Environmental Health Hazard Assessment, 2005.
Chronic Reference Exposure Levels Adopted by OEHHA as of December
2008. https://www.oehha.ca.gov/air/chronic_rels.
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F. What analysis of environmental justice did we conduct?
As explained in section IV.A of this preamble, we assessed the
impacts to various demographic groups. The methodology and the results
of the analyses are described in the Risk and Technology Review--
Analysis of Socio-Economic Factors for Populations Living Near
Ferroalloys Facilities, which is available in the docket.
Based on that assessment, we conclude that this final rule will
reduce the number of people exposed to elevated risks, from
approximately 41,000, to about 26,000 people exposed to a potential
cancer risk greater than or equal to 1-in-1 million and from 1,300 to
zero people exposed to a potential chronic noncancer hazard level of 1.
Based on this analysis, the EPA has determined that these final rule
requirements will not have disproportionately high and adverse human
health or environmental effects on minority or low-income populations
because it increases the level of environmental protection for all
affected populations. See Section VI.J of this preamble for more
information.
G. What analysis of children's environmental health did we conduct?
This action is not subject to Executive Order 13045 (62 FR 19885,
April 23, 1997) because the Agency does not believe the environmental
health risks or safety risks addressed by this action present a
disproportionate risk to children. The report, Analysis of Socio-
Economic Factors for Populations Living Near Ferroalloys Facilities,
which is available in the docket, shows that, prior to the
implementation of the provisions included in this final rule, on a
nationwide basis, there are approximately 41,000 people exposed to a
cancer risk at or above 1-in-1 million and approximately 1,300 people
exposed to a chronic noncancer TOSHI greater than 1 due to emissions
from the source category. The percentages for all demographic groups
(with the exception of those ages 65 and older, which is only slightly
higher than the national average), including children 18 years and
younger, are similar to or lower than their respective nationwide
percentages. Further, implementation of the provisions included in this
action is expected to significantly reduce the number of at-risk people
due to HAP emissions from these sources (from approximately 41,000 to
about 26,000 for cancer risks and from 1,300 to zero for chronic
noncancer hazards), providing significant benefit to all demographic
groups.
This rule is expected to reduce environmental impacts for everyone,
including children. This action establishes emissions limits at the
levels based on MACT, as required by the CAA. Based on our analysis, we
believe that this rule does not present a disproportionate risk to
children because it increases the level of environmental protection for
all affected populations.
VI. Statutory and Executive Order Reviews
Additional information about these statutes and Executive Orders
can be found at https://www2.epa.gov/laws-regulations/laws-and-executive-orders.
A. Executive Orders 12866: Regulatory Planning and Review and Executive
Order 13563: Improving Regulation and Regulatory Review
This action is not a significant regulatory action and was,
therefore, not submitted to the Office of Management and Budget (OMB)
for review.
B. Paperwork Reduction Act (PRA)
The information collection activities in this rule have been
submitted for approval to the OMB under the PRA. The ICR document that
the EPA prepared has been assigned EPA ICR number 2488.01. You can find
a copy of the ICR in the docket for this rule, and it is briefly
summarized here. The information collection requirements are not
enforceable until OMB approves them.
The information requirements in this rulemaking are based on the
notification, recordkeeping, and reporting requirements in the NESHAP
General Provisions (40 CFR part 63, subpart A), which are mandatory for
all operators subject to national emission standards. These
notifications, reports, and records are essential in determining
compliance, and are specifically authorized by CAA section 114 (42
U.S.C. 7414). All information submitted to the EPA pursuant to the
recordkeeping and reporting requirements for which a claim of
confidentiality is made is safeguarded according to agency policies set
forth in 40 CFR part 2, subpart B.
Respondents/affected entities: New and existing ferroalloys
production facilities that produce FeMn and SiMn and are either major
sources of HAP emissions or are co-located at major sources of HAP.
Respondent's obligation to respond: Mandatory (42 U.S.C. 7414).
Estimated number of respondents: 2.
Frequency of response: Semiannual.
Total estimated burden: 707 hours (per year). Burden is defined at
5 CFR 1320.3(b).
Total estimated cost: $0.85 million (per year), includes $0.78
million annualized capital or operation & maintenance costs.
An agency may not conduct or sponsor, and a person is not required
to respond to, a collection of information unless it displays a
currently valid OMB control number. The OMB control numbers for the
EPA's regulations in 40 CFR are listed in 40 CFR part 9. When OMB
approves this ICR, the agency will announce that approval in the
Federal Register and publish a technical amendment to 40 CFR part 9 to
display the OMB control number for the approved information collection
activities contained in this final rule.
C. Regulatory Flexibility Act (RFA)
I certify that this action will not have a significant economic
impact on a substantial number of small entities under the RFA. The
small entities subject to the requirements of this action are
businesses that can be classified as small firms using the Small
Business Administration size standards for their respective industries.
The agency has determined that neither of the companies affected by
this rule is considered to be a small entity. Details of this analysis
are presented in the memorandum, Economic Impact Analysis for Risk and
Technology Review: Ferroalloys Production Source
[[Page 37389]]
Category, which is available in the docket for this action.
D. Unfunded Mandates Reform Act (UMRA)
This action does not contain an unfunded mandate of $100 million or
more as described in UMRA, 2 U.S.C. 1531-1538, and does not
significantly or uniquely affect small governments. The action imposes
no enforceable duty on any state, local, or tribal governments, or on
the private sector.
E. Executive Order 13132: Federalism
This action does not have federalism implications. It will not have
substantial direct effects on the states, on the relationship between
the national government and the states, or on the distribution of power
and responsibilities among the various levels of government.
F. Executive Order 13175: Consultation and Coordination With Indian
Tribal Governments
This action does not have tribal implications as specified in
Executive Order 13175. There are no ferroalloys production facilities
that are owned or operated by 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
This action is not subject to Executive Order 13045 because it is
not economically significant as defined in Executive Order 12866, and
because the EPA does not believe the environmental health or safety
risks addressed by this action present a disproportionate risk to
children. This action's health and risk assessments are contained in
the Residual Risk Assessment for the Ferroalloys Production Source
Category in Support of the 2015 Risk and Technology Review Final Rule
document, which is available in the docket for this action, and are
discussed in section V.G of this preamble.
H. Executive Order 13211: Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution or Use
This action is not subject to Executive Order 13211 because it is
not a significant regulatory action under Executive Order 12866.
I. National Technology Transfer and Advancement Act and 1 CFR Part 51
This final rule involves technical standards. EPA decided to use
ASME PTC 19.10-1981, ``Flue and Exhaust Gas Analyses,'' for its manual
methods of measuring the oxygen or carbon dioxide content of the
exhaust gas. These parts of ASME PTC 19.10-1981 are acceptable
alternatives to EPA Method 3B. This standard is available from the
American Society of Mechanical Engineers (ASME), Three Park Avenue, New
York, NY 10016-5990.
The EPA has also decided to use ASTM D7520-13, Standard Test Method
for Determining the Opacity in a Plume in an Outdoor Ambient
Atmosphere, for measuring opacity from the shop buildings. This
standard is an acceptable alternative to EPA Method 9 and is available
from the American Society for Testing and Materials (ASTM), 100 Barr
Harbor Drive, Post Office Box C700, West Conshohocken, PA 19428-2959.
See https://www.astm.org/.
In addition, the EPA has decided to use California Air Resources
Board Method 429, Determination of Polycyclic Aromatic Hydrocarbon
(PAH) Emissions from Stationary Sources for measuring PAH emissions
from the furnace control device. This method is an acceptable
alternative to EPA Method 0010 and is available from the California Air
Resources Board (CARB), Engineering and Certification Branch, 1001 I
Street, P.O. Box 2815, Sacramento, CA 95812-2815. See https://www.arb.ca.gov/testmeth/vol3/M_429.pdf.
The EPA has also decided to use EPA Methods 1, 2, 3A, 3B, 4, 5, 5D,
10, 26A, 29, 30B, 316 of 40 CFR part 60, appendix A. No applicable VCS
were identified for EPA Methods 30B, 5D, 316.
Under 40 CFR 63.7(f) and 40 CFR 63.8(f) of subpart A of the 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 this final rule.
J. Executive Order 12898: Federal Actions To Address Environmental
Justice in Minority Populations and Low-Income Populations
The EPA has determined that the current health risks posed by
emissions from this source category are unacceptable. There are up to
41,000 people living in close proximity to the two facilities that are
currently subject to health risks which may not be considered
negligible (i.e., cancer risks greater than 1-in-1 million or chronic
noncancer TOSHI greater than 1) due to emissions from this source
category. The demographic makeup of this population is similar to the
national distribution for all demographic groups, with the exception of
those ages 65 and older, which is slightly higher than the national
average. This final rule will reduce the number of people in this
group, from approximately 41,000, to about 26,000 people exposed to a
cancer risk greater than or equal to 1-in-1 million and from 1,300 to
zero people for a chronic noncancer hazard index of 1. The EPA believes
the human health or environmental risk addressed by this action will
not have potential disproportionately high and adverse human health or
environmental effects on minority, low-income, or indigenous
populations because it increases the level of environmental protection
for all affected populations. The results of this evaluation are
contained in section IV.A of this preamble. A copy of this methodology
and the results of the demographic analysis are included in a technical
report, Risk and Technology Review--Analysis of Socio-Economic Factors
for Populations Living Near Ferroalloys Facilities, which is available
in the docket for this action.
K. Congressional Review Act (CRA)
This action is subject to the CRA, and the EPA will submit a rule
report to each House of the Congress and to the Comptroller General of
the United States. This action is not a ``major rule'' as defined by 5
U.S.C. 804(2).
List of Subjects for 40 CFR Part 63
Environmental protection, Administrative practice and procedures,
Air pollution control, Hazardous substances, Incorporation by
reference, Intergovernmental relations, Reporting and recordkeeping
requirements.
Dated: May 28, 2015.
Gina McCarthy,
Administrator.
For the reasons stated in the preamble, the Environmental
Protection Agency is amending title 40, chapter I, part 63 of the Code
of Federal Regulations (CFR) as follows:
PART 63--NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS
FOR SOURCE CATEGORIES
0
1. The authority citation for part 63 continues to read as follows:
Authority: 42 U.S.C. 7401 et seq.
Subpart A--General Provisions
0
2. Section 63.14 is amended:
0
a. By revising paragraph (f)(1);
[[Page 37390]]
0
b. By redesignating paragraphs (g)(87) through (94) as paragraphs
(g)(88) through (95), respectively;
0
c. By adding new paragraph (g)(87);
0
d. By revising paragraph (j) introductory text;
0
e. By redesignating paragraphs (j)(1) through (3) as paragraphs (j)(2)
through (4), respectively; and
0
f. By adding new paragraph (j)(1).
The revisions and additions read as follows:
Sec. 63.14 Incorporations by reference.
* * * * *
(f) * * *
(1) ANSI/ASME PTC 19.10-1981, Flue and Exhaust Gas Analyses [Part
10, Instruments and Apparatus], issued August 31, 1981, IBR approved
for Sec. Sec. 63.309(k), 63.457(k), 63.772(e) and (h), 63.865(b),
63.1282(d) and (g), 63.1625(b), 63.3166(a), 63.3360(e), 63.3545(a),
63.3555(a), 63.4166(a), 63.4362(a), 63.4766(a), 63.4965(a), 63.5160(d),
table 4 to subpart UUUU, 63.9307(c), 63.9323(a), 63.11148(e),
63.11155(e), 63.11162(f), 63.11163(g), 63.11410(j), 63.11551(a),
63.11646(a), and 63.11945, table 5 to subpart DDDDD, table 4 to subpart
JJJJJ, tables 4 and 5 of subpart UUUUU, and table 1 to subpart ZZZZZ.
* * * * *
(g) * * *
(87) ASTM D7520-13, ``Standard Test Method for Determining the
Opacity in a Plume in an Outdoor Ambient Atmosphere,'' Approved
December 1, 2013, IBR approved for Sec. Sec. 63.1625(b).
* * * * *
(j) California Air Resources Board (CARB), 1001 I Street, P.O. Box
2815, Sacramento, CA 95812-2815, Telephone (916) 327-0900, https://www.arb.ca.gov/.
(1) Method 429, Determination of Polycyclic Aromatic Hydrocarbon
(PAH) Emissions from Stationary Sources, Adopted September 12, 1989,
Amended July 28, 1997, IBR approved for Sec. 63.1625(b).
* * * * *
Subpart XXX--National Emission Standards for Hazardous Air
Pollutants for Ferroalloys Production: Ferromanganese and
Silicomanganese
0
3. Sections 63.1620 through 63.1629 are added to read as follows:
Sec.
63.1620 Am I subject to this subpart?
63.1621 What are my compliance dates?
63.1622 What definitions apply to this subpart?
63.1623 What are the emissions standards for new, reconstructed and
existing facilities?
63.1624 What are the operational and work practice standards for
new, reconstructed, and existing facilities?
63.1625 What are the performance test and compliance requirements
for new, reconstructed, and existing facilities?
63.1626 What monitoring requirements must I meet?
63.1627 What notification requirements must I meet?
63.1628 What recordkeeping and reporting requirements must I meet?
63.1629 Who implements and enforces this subpart?
* * * * *
Sec. 63.1620 Am I subject to this subpart?
(a) You are subject to this subpart if you own or operate a new or
existing ferromanganese and/or silicomanganese production facility that
is a major source or is co-located at a major source of hazardous air
pollutant emissions.
(b) You are subject to this subpart if you own or operate any of
the following equipment as part of a ferromanganese and/or
silicomanganese production facility:
(1) Electric arc furnace;
(2) Casting operations;
(3) Metal oxygen refining (MOR) process;
(4) Crushing and screening operations;
(5) Outdoor fugitive dust sources.
(c) A new affected source is any of the equipment listed in
paragraph (b) of this section for which construction or reconstruction
commenced after June 30, 2015.
(d) Table 1 of this subpart specifies the provisions of subpart A
of this part that apply to owners and operators of ferromanganese and
silicomanganese production facilities subject to this subpart.
(e) If you are subject to the provisions of this subpart, you are
also subject to title V permitting requirements under 40 CFR part 70 or
71, as applicable.
(f) Emission standards in this subpart apply at all times.
Sec. 63.1621 What are my compliance dates?
(a) Existing affected sources must be in compliance with the
provisions specified in Sec. Sec. 63.1620 through 63.1629 no later
than June 30, 2017.
(b) Affected sources in existence prior to June 30, 2015 must be in
compliance with the provisions specified in Sec. Sec. 63.1650 through
63.1661 by November 21, 2001 and until June 30, 2017. As of June 30,
2017, the provisions of Sec. Sec. 63.1650 through 63.1661 cease to
apply to affected sources in existence prior to June 30, 2015. The
provisions of Sec. Sec. 63.1650 through 63.1661 remain enforceable at
a source for its activities prior to June 30, 2017.
(c) If you own or operate a new affected source that commences
construction or reconstruction after November 23, 2011, you must comply
with the requirements of this subpart by June 30, 2015, or upon startup
of operations, whichever is later.
Sec. 63.1622 What definitions apply to this subpart?
Terms in this subpart are defined in the Clean Air Act (Act), in
subpart A of this part, or in this section as follows:
Bag leak detection system means a system that is capable of
continuously monitoring particulate matter (dust) loadings in the
exhaust of a baghouse in order to detect bag leaks and other upset
conditions. A bag leak detection system includes, but is not limited
to, an instrument that operates on triboelectric, light scattering,
light transmittance, or other effect to continuously monitor relative
particulate matter loadings.
Capture system means the collection of components used to capture
the gases and fumes released from one or more emissions points and then
convey the captured gas stream to a control device or to the
atmosphere. A capture system may include, but is not limited to, the
following components as applicable to a given capture system design:
Duct intake devices, hoods, enclosures, ductwork, dampers, manifolds,
plenums, fans and roofline ventilation systems.
Casting means the period of time from when molten ferroalloy is
removed from the tapping station until the pouring into casting molds
or beds is completed. This includes the following operations: Pouring
alloy from one ladle to another, slag separation, slag removal and
ladle transfer by crane, truck, or other conveyance.
Crushing and screening equipment means the crushers, grinders,
mills, screens and conveying systems used to crush, size and prepare
for packing manganese-containing materials, including raw materials,
intermediate products and final products.
Electric arc furnace means any furnace where electrical energy is
converted to heat energy by transmission of current between electrodes
partially submerged in the furnace charge. The furnace may be of an
open, semi-sealed, or sealed design.
Furnace process cycle means the period in which the furnace is
tapped to the time in which the furnace is tapped again and includes
periods of charging, smelting, tapping, casting and ladle raking. For
multiple furnaces operating within a single shop building, furnace
process cycle means a period sufficient
[[Page 37391]]
to capture a full cycle of charging, smelting, tapping, casting and
ladle raking for each furnace within the shop building.
Ladle treatment means a post-tapping process including metal and
alloy additions where chemistry adjustments are made in the ladle after
furnace smelting to achieve a specified product.
Local ventilation means hoods, ductwork, and fans designed to
capture process fugitive emissions close to the area where the
emissions are generated (e.g., tap hoods).
Metal oxygen refining (MOR) process means the reduction of the
carbon content of ferromanganese through the use of oxygen.
Outdoor fugitive dust source means a stationary source from which
hazardous air pollutant-bearing particles are discharged to the
atmosphere due to wind or mechanical inducement such as vehicle
traffic. Fugitive dust sources include plant roadways, yard areas and
outdoor material storage and transfer operation areas.
Plant roadway means any area at a ferromanganese and
silicomanganese production facility that is subject to plant mobile
equipment, such as forklifts, front end loaders, or trucks, carrying
manganese-bearing materials. Excluded from this definition are employee
and visitor parking areas, provided they are not subject to traffic by
plant mobile equipment.
Process fugitive emissions source means a source of hazardous air
pollutant emissions that is associated with a ferromanganese or
silicomanganese production facility and is not a fugitive dust source
or a stack emissions source. Process fugitive sources include emissions
that escape capture from the electric arc furnace, tapping operations,
casting operations, ladle treatment, MOR or crushing and screening
equipment.
Roofline ventilation system means an exhaust system designed to
evacuate process fugitive emissions that collect in the roofline area
to a control device.
Shop building means the building which houses one or more electric
arc furnaces or other processes that generate process fugitive
emissions.
Shutdown means the cessation of operation of an affected source for
any purpose.
Startup means the setting in operation of an affected source for
any purpose.
Tapping emissions means the gases and emissions associated with
removal of product from the electric arc furnace under normal operating
conditions, such as removal of metal under normal pressure and movement
by gravity down the spout into the ladle and filling the ladle.
Tapping period means the time from when a tap hole is opened until
the time a tap hole is closed.
Sec. 63.1623 What are the emissions standards for new, reconstructed
and existing facilities?
(a) Electric arc furnaces. You must install, operate and maintain
an effective capture system that collects the emissions from each
electric arc furnace operation and conveys the collected emissions to a
control device for the removal of the pollutants specified in the
emissions standards specified in paragraphs (a)(1) through (5) of this
section.
(1) Particulate matter emissions. (i) You must not discharge
exhaust gases from each electric arc furnace operation containing
particulate matter in excess of 4.0 milligrams per dry standard cubic
meter (mg/dscm) into the atmosphere from any new or reconstructed
electric arc furnace.
(ii) You must not discharge exhaust gases from each electric arc
furnace operation containing particulate matter in excess of 25 mg/dscm
into the atmosphere from any existing electric arc furnace.
(2) Mercury emissions. (i) You must not discharge exhaust gases
from each electric arc furnace operation containing mercury emissions
in excess of 13 micrograms per dry standard cubic meter ([mu]g/dscm)
into the atmosphere from any new or reconstructed electric arc furnace
when producing ferromanganese.
(ii) You must not discharge exhaust gases from each electric arc
furnace operation containing mercury emissions in excess of 130 [mu]g/
dscm into the atmosphere from any existing electric arc furnace when
producing ferromanganese.
(iii) You must not discharge exhaust gases from each electric arc
furnace operation containing mercury emissions in excess of 4 [mu]g/
dscm into the atmosphere from any new or reconstructed electric arc
furnace when producing silicomanganese.
(iv) You must not discharge exhaust gases from each electric arc
furnace operation containing mercury emissions in excess of 12 [mu]g/
dscm into the atmosphere from any existing electric arc furnace when
producing silicomanganese.
(3) Polycyclic aromatic hydrocarbon emissions. (i) You must not
discharge exhaust gases from each electric arc furnace operation
containing polycyclic aromatic hydrocarbon emissions in excess of
12,000 [mu]g/dscm into the atmosphere from any new or reconstructed
electric arc furnace when producing ferromanganese.
(ii) You must not discharge exhaust gases from each electric arc
furnace operation containing polycyclic aromatic hydrocarbon emissions
in excess of 12,000 [mu]g/dscm into the atmosphere from any existing
electric arc furnace when producing ferromanganese.
(iii) You must not discharge exhaust gases from each electric arc
furnace operation containing polycyclic aromatic hydrocarbon emissions
in excess of 72 [mu]g/dscm into the atmosphere from any new or
reconstructed electric arc furnace when producing silicomanganese.
(iv) You must not discharge exhaust gases from each electric arc
furnace operation containing polycyclic aromatic hydrocarbon emissions
in excess of 130 [mu]g/dscm into the atmosphere from any existing
electric arc furnace when producing silicomanganese.
(4) Hydrochloric acid emissions. (i) You must not discharge exhaust
gases from each electric arc furnace operation containing hydrochloric
acid emissions in excess of 180 [mu]g/dscm into the atmosphere from any
new or reconstructed electric arc furnace.
(ii) You must not discharge exhaust gases from each electric arc
furnace operation containing hydrochloric acid emissions in excess of
1,100 [mu]g/dscm into the atmosphere from any existing electric arc
furnace.
(5) Formaldehyde emissions. You must not discharge exhaust gases
from each electric arc furnace operation containing formaldehyde
emissions in excess of 201 [mu]g/dscm into the atmosphere from any new,
reconstructed or existing electric arc furnace.
(b) Process fugitive emissions. (1) You must install, operate and
maintain a capture system that is designed to collect 95 percent or
more of the emissions from process fugitive emissions sources and
convey the collected emissions to a control device that is demonstrated
to meet the applicable emission limit specified in paragraph (a)(1) or
(c) of this section.
(2) The determination of the overall capture must be demonstrated
as required by Sec. 63.1624(a).
(3) Unless you meet the criteria of paragragh (b)(3)(iii) of this
section, you must not cause the emissions exiting from a shop building
to exceed an average of 8 percent opacity over a furnace or MOR process
cycle.
(i) This 8 percent opacity requirement is determined by averaging
the
[[Page 37392]]
individual opacity readings observed during the furnace or MOR process
cycle.
(ii) An individual opacity reading shall be determined as the
average of 24 consecutive images recorded at 15-second intervals with
the opacity values from each individual digital image rounded to the
nearest 5 percent.
(iii) If the average opacity from the shop building is greater than
8 percent opacity during an observed furnace or MOR process cycle, the
opacity of two more additional furnace or MOR process cycles must be
observed within 7 days and the average of the individual opacity
readings during the three observation periods must be less than 8
percent opacity.
(iv) At no time during operation may the average of any two
consecutive individual opacity readings be greater than 20 percent
opacity.
(c) Local ventilation emissions. If you operate local ventilation
to capture tapping, casting, or ladle treatment emissions and direct
them to a control device other than one associated with the electric
arc furnace, you must not discharge into the atmosphere any captured
emissions containing particulate matter in excess of 4.0 mg/dscm.
(d) MOR process. You must not discharge into the atmosphere from
any new, reconstructed or existing MOR process exhaust gases containing
particulate matter in excess of 3.9 mg/dscm.
(e) Crushing and screening equipment. You must not discharge into
the atmosphere from any new, reconstructed, or existing piece of
equipment associated with crushing and screening exhaust gases
containing particulate matter in excess of 13 mg/dscm.
(f) At all times, you must operate and maintain any affected
source, including associated air pollution control equipment and
monitoring equipment, in a manner consistent with safety and good air
pollution control practices for minimizing emissions. Determination of
whether such operation and maintenance procedures are being used will
be based on information available to the Administrator that may
include, but is not limited to, monitoring results, review of operation
and maintenance procedures, review of operation and maintenance records
and inspection of the source.
Sec. 63.1624 What are the operational and work practice standards for
new, reconstructed, and existing facilities?
(a) Process fugitive emissions sources. (1) You must prepare, and
at all times operate according to, a process fugitive emissions
ventilation plan that documents the equipment and operations designed
to effectively capture process fugitive emissions. The plan will be
deemed to achieve effective capture if it consists of the following
elements:
(i) Documentation of engineered hoods and secondary fugitive
capture systems designed according to the most recent, at the time of
construction, ventilation design principles recommended by the American
Conference of Governmental Industrial Hygienists (ACGIH). The process
fugitive emissions capture systems must be designed to achieve
sufficient air changes to evacuate the collection area frequently
enough to ensure process fugitive emissions are effectively collected
by the ventilation system and ducted to the control device(s). The
required ventilation systems should also use properly positioned
hooding to take advantage of the inherent air flows of the source and
capture systems that minimize air flows while also intercepting natural
air flows or creating air flows to contain the fugitive emissions.
Include a schematic for each building indicating duct sizes and
locations, hood sizes and locations, control device types, size and
locations and exhaust locations. The design plan must identify the key
operating parameters and measurement locations to ensure proper
operation of the system and establish monitoring parameter values that
reflect effective capture.
(ii) List of critical maintenance actions and the schedule to
conduct them.
(2) You must submit a copy of the process fugitive emissions
ventilation plan to the designated permitting authority on or before
the applicable compliance date for the affected source as specified in
Sec. 63.1621 in electronic format and whenever an update is made to
the plan. The requirement for you to operate the facility according to
the written process fugitives ventilation plan and specifications must
be incorporated in the operating permit for the facility that is issued
by the designated permitting authority under part 70 or 71 of this
chapter, as applicable.
(3) You must update the information required in paragraphs (a)(1)
and (2) of this section every 5 years or whenever there is a
significant change in variables that affect process fugitives
ventilation design such as the addition of a new process.
(b) Outdoor fugitive dust sources. (1) You must prepare, and at all
times operate according to, an outdoor fugitive dust control plan that
describes in detail the measures that will be put in place to control
outdoor fugitive dust emissions from the individual fugitive dust
sources at the facility.
(2) You must submit a copy of the outdoor fugitive dust control
plan to the designated permitting authority on or before the applicable
compliance date for the affected source as specified in Sec. 63.1621.
The requirement for you to operate the facility according to a written
outdoor fugitive dust control plan must be incorporated in the
operating permit for the facility that is issued by the designated
permitting authority under part 70 or 71 of this chapter, as
applicable.
(3) You may use existing manuals that describe the measures in
place to control outdoor fugitive dust sources required as part of a
state implementation plan or other federally enforceable requirement
for particulate matter to satisfy the requirements of paragraph (b)(1)
of this section.
Sec. 63.1625 What are the performance test and compliance
requirements for new, reconstructed, and existing facilities?
(a) Performance testing. (1) All performance tests must be
conducted according to the requirements in Sec. 63.7.
(2) Each performance test in paragraphs (c)(1) and (2) of this
section must consist of three separate and complete runs using the
applicable test methods.
(3) Each run must be conducted under conditions that are
representative of normal process operations.
(4) Performance tests conducted on air pollution control devices
serving electric arc furnaces must be conducted such that at least one
tapping period, or at least 20 minutes of a tapping period, whichever
is less, is included in at least two of the three runs. The sampling
time for each run must be at least three times the average tapping
period of the tested furnace, but no less than 60 minutes.
(5) You must conduct the performance tests specified in paragraph
(c) of this section under such conditions as the Administrator
specifies based on representative performance of the affected source
for the period being tested. Upon request, you must make available to
the Administrator such records as may be necessary to determine the
conditions of performance tests.
(b) Test methods. The following test methods in appendices of part
60 or 63 of this chapter or as specified elsewhere must be used to
determine compliance with the emission standards.
[[Page 37393]]
(1) Method 1 of appendix A-1 of 40 CFR part 60 to select the
sampling port location and the number of traverse points.
(2) Method 2 of appendix A-1 of 40 CFR part 60 to determine the
volumetric flow rate of the stack gas.
(3)(i) Method 3A or 3B of appendix A-2 of 40 CFR part 60 (with
integrated bag sampling) to determine the outlet stack and inlet oxygen
and CO2 content.
(ii) You must measure CO2 concentrations at both the
inlet and outlet of the positive pressure fabric filter in conjunction
with the pollutant sampling in order to determine isokinetic sampling
rates.
(iii) As an alternative to EPA Reference Method 3B, ASME PTC-19-10-
1981-Part 10 may be used (incorporated by reference, see Sec. 63.14).
(4) Method 4 of appendix A-3 of 40 CFR part 60 to determine the
moisture content of the stack gas.
(5)(i) Method 5 of appendix A-3 of 40 CFR part 60 to determine the
particulate matter concentration of the stack gas for negative pressure
baghouses and positive pressure baghouses with stacks.
(ii) Method 5D of appendix A-3 of 40 CFR part 60 to determine
particulate matter concentration and volumetric flow rate of the stack
gas for positive pressure baghouses without stacks.
(iii) The sample volume for each run must be a minimum of 4.0 cubic
meters (141.2 cubic feet). For Method 5 testing only, you may choose to
collect less than 4.0 cubic meters per run provided that the filterable
mass collected (i.e., net filter mass plus mass of nozzle, probe and
filter holder rinses) is equal to or greater than 10 mg. If the total
mass collected for two of three of the runs is less than 10 mg, you
must conduct at least one additional test run that produces at least 10
mg of filterable mass collected (i.e., at a greater sample volume).
Report the results of all test runs.
(6) Method 30B of appendix A-8 of 40 CFR part 60 to measure
mercury. Apply the minimum sample volume determination procedures as
per the method.
(7)(i) Method 26A of appendix A-8 of 40 CFR part 60 to determine
outlet stack or inlet hydrochloric acid concentration.
(ii) Collect a minimum volume of 2 cubic meters.
(8)(i) Method 316 of appendix A of this part to determine outlet
stack or inlet formaldehyde.
(ii) Collect a minimum volume of 1.0 cubic meter.
(9) ASTM D7520-13 to determine opacity (incorporated by reference,
see Sec. 63.14) with the following conditions:
(i) During the digital camera opacity technique (DCOT)
certification procedure outlined in Section 9.2 of ASTM D7520-13, you
or the DCOT vendor must present the plumes in front of various
backgrounds of color and contrast representing conditions anticipated
during field use such as blue sky, trees and mixed backgrounds (clouds
and/or a sparse tree stand).
(ii) You must have standard operating procedures in place including
daily or other frequency quality checks to ensure the equipment is
within manufacturing specifications as outlined in Section 8.1 of ASTM
D7520-13.
(iii) You must follow the recordkeeping procedures outlined in
Sec. 63.10(b)(1) for the DCOT certification, compliance report, data
sheets and all raw unaltered JPEGs used for opacity and certification
determination.
(iv) You or the DCOT vendor must have a minimum of four (4)
independent technology users apply the software to determine the
visible opacity of the 300 certification plumes. For each set of 25
plumes, the user may not exceed 20 percent opacity for any one reading
and the average error must not exceed 7.5 percent opacity.
(v) Use of this method does not provide or imply a certification or
validation of any vendor's hardware or software. The onus to maintain
and verify the certification and/or training of the DCOT camera,
software and operator in accordance with ASTM D7520-13 and these
requirements is on the facility, DCOT operator and DCOT vendor.
(10) California Air Resources Board (CARB) Method 429 (incorporated
by reference, see Sec. 63.14).
(11) The owner or operator may use alternative measurement methods
approved by the Administrator following the procedures described in
Sec. 63.7(f).
(c) Compliance demonstration with the emission standards--(1)
Initial performance test. You must conduct an initial performance test
for air pollution control devices or vent stacks subject to Sec.
63.1623(a), (b)(1), and (c) through (e) to demonstrate compliance with
the applicable emission standards.
(2) Periodic performance test. (i) You must conduct annual
particulate matter tests for wet scrubber air pollution control devices
subject to Sec. 63.1623(a)(1) to demonstrate compliance with the
applicable emission standards.
(ii) You must conduct particulate matter tests every 5 years for
fabric filter air pollution control devices subject to Sec.
63.1623(a)(1) to demonstrate compliance with the applicable emission
standards.
(iii) You must conduct annual mercury performance tests for wet
scrubber and fabric filter air pollution control devices or vent stacks
subject to Sec. 63.1623(a)(2) to demonstrate compliance with the
applicable emission standards.
(iv) You must conduct PAH performance tests for wet scrubber and
fabric filter air pollution control devices or vent stacks subject to
Sec. 63.1623(a)(3) to demonstrate compliance with the applicable
emission standards.
(A) For furnaces producing silicomanganese, you must conduct a PAH
performance test every 5 years for each furnace that produces
silicomanganese subject to Sec. 63.1623(a)(3).
(B) For furnaces producing ferromanganese, you must conduct a PAH
performance test every 3 months or 2,190 cumulative hours of
ferromanganese production for each furnace subject to Sec.
63.1623(a)(3).
(C) If a furnace producing ferromanganese demonstrates compliance
with four consecutive PAH tests, the owner/operator may petition the
permitting authority to request reduced frequency of testing to
demonstrate compliance with the PAH emission standards. However, this
PAH compliance testing cannot be reduced to less than once per year.
(v) You must conduct ongoing performance tests every 5 years for
air pollution control devices or vent stacks subject to Sec.
63.1623(a)(4), (a)(5), (b)(1), and (c) through (e) to demonstrate
compliance with the applicable emission standards.
(3) Compliance is demonstrated for all sources performing emissions
tests if the average concentration for the three runs comprising the
performance test does not exceed the standard.
(4) Operating limits. You must establish parameter operating limits
according to paragraphs (c)(4)(i) through (iv) of this section. Unless
otherwise specified, compliance with each established operating limit
shall be demonstrated for each 24-hour operating day.
(i) For a wet particulate matter scrubber, you must establish the
minimum liquid flow rate and pressure drop as your operating limits
during the three-run performance test. If you use a wet particulate
matter scrubber and you conduct separate performance tests for
particulate matter, you must establish one set of minimum liquid flow
rate and pressure drop operating limits. If you conduct multiple
performance tests, you must set the minimum liquid flow rate and
pressure drop operating limits at the highest minimum hourly average
[[Page 37394]]
values established during the performance tests.
(ii) For a wet acid gas scrubber, you must establish the minimum
liquid flow rate and pH, as your operating limits during the three-run
performance test. If you use a wet acid gas scrubber and you conduct
separate performance tests for hydrochloric acid, you must establish
one set of minimum liquid flow rate and pH operating limits. If you
conduct multiple performance tests, you must set the minimum liquid
flow rate and pH operating limits at the highest minimum hourly average
values established during the performance tests.
(iii) For emission sources with fabric filters that choose to
demonstrate continuous compliance through bag leak detection systems
you must install a bag leak detection system according to the
requirements in Sec. 63.1626(d) and you must set your operating limit
such that the sum duration of bag leak detection system alarms does not
exceed 5 percent of the process operating time during a 6-month period.
(iv) If you choose to demonstrate continuous compliance through a
particulate matter CEMS, you must determine an operating limit
(particulate matter concentration in mg/dscm) during performance
testing for initial particulate matter compliance. The operating limit
will be the average of the PM filterable results of the three Method 5
or Method 5D of appendix A-3 of 40 CFR part 60 performance test runs.
To determine continuous compliance, the hourly average PM
concentrations will be averaged on a rolling 30 operating day basis.
Each 30 operating day average will have to meet the PM operating limit.
(d) Compliance demonstration with shop building opacity standards.
(1)(i) If you are subject to Sec. 63.1623(b), you must conduct opacity
observations of the shop building to demonstrate compliance with the
applicable opacity standards according to Sec. 63.6(h)(5), which
addresses conducting opacity or visible emission observations.
(ii) You must conduct the opacity observations according to ASTM
D7520-13 (incorporated by reference, see Sec. 63.14), for a period
that includes at least one complete furnace process cycle for each
furnace.
(iii) For a shop building that contains more than one furnace, you
must conduct the opacity observations according to ASTM D7520-13, for a
period that includes one tapping period from each furnace located in
the shop building.
(iv) You must conduct the opacity observations according to ASTM
D7520-13, for a one hour period that includes at least one pouring for
each MOR located in the shop building.
(v) You must conduct the opacity observations at least once per
week for each shop building containing one or more furnaces or MOR.
(vi) You may reduce the frequency of observations to once per month
for each shop building that demonstrates compliance with the weekly 8-
percent opacity limit for 26 consecutive complete observations that
span a period of at least 26 weeks. Any monthly observation in excess
of 8-percent opacity will return that shop building opacity observation
to a weekly compliance schedule. You may reduce the frequency of
observations again to once per month for each shop building that
demonstrates compliance with the weekly 8-percent opacity limit after
another 26 consecutive complete observations that span a period of at
least 26 weeks.
(2) You must determine shop building opacity operating parameters
based on either monitoring data collected during the compliance
demonstration or established in an engineering assessment.
(i) If you choose to establish parameters based on the initial
compliance demonstration, you must simultaneously monitor parameter
values for one of the following: The capture system fan motor amperes
and all capture system damper positions, the total volumetric flow rate
to the air pollution control device and all capture system damper
positions, or volumetric flow rate through each separately ducted hood
that comprises the capture system. Subsequently you must monitor these
parameters according to Sec. 63.1626(g) and ensure they remain within
10 percent of the value recorded during the compliant opacity readings.
(ii) If you choose to establish parameters based on an engineering
assessment, then a design analysis shall include, for example,
specifications, drawings, schematics and ventilation system diagrams
prepared by the owner or operator or capture or control system
manufacturer or vendor that describes the shop building opacity system
ventilation design based on acceptable engineering texts. The design
analysis shall address vent stream characteristics and ventilation
system design operating parameters such as fan amps, damper position,
flow rate and/or other specified parameters.
(iii) You may petition the Administrator to reestablish these
parameter ranges whenever you can demonstrate to the Administrator's
satisfaction that the electric arc furnace or MOR operating conditions
upon which the parameter ranges were previously established are no
longer applicable. The values of these parameter ranges determined
during the most recent demonstration of compliance must be maintained
at the appropriate level for each applicable period.
(3) You will demonstrate continuing compliance with the opacity
standards by following the monitoring requirements specified in Sec.
63.1626(g) and the reporting and recordkeeping requirements specified
in Sec. 63.1628(b)(5).
(e) Compliance demonstration with the operational and work practice
standards--(1) Process fugitive emissions sources. You will demonstrate
compliance by developing and maintaining a process fugitives
ventilation plan, by reporting any deviations from the plan and by
taking necessary corrective actions to correct deviations or
deficiencies.
(2) Outdoor fugitive dust sources. You will demonstrate compliance
by developing and maintaining an outdoor fugitive dust control plan, by
reporting any deviations from the plan and by taking necessary
corrective actions to correct deviations or deficiencies.
(3) Baghouses equipped with bag leak detection systems. You will
demonstrate compliance with the bag leak detection system requirements
by developing an analysis and supporting documentation demonstrating
conformance with EPA guidance and specifications for bag leak detection
systems in Sec. 60.57c(h) of this chapter.
Sec. 63.1626 What monitoring requirements must I meet?
(a) Baghouse monitoring. You must prepare, and at all times operate
according to, a standard operating procedures manual that describes in
detail procedures for inspection, maintenance and bag leak detection
and corrective action plans for all baghouses (fabric filters or
cartridge filters) that are used to control process vents, process
fugitive, or outdoor fugitive dust emissions from any source subject to
the emissions standards in Sec. 63.1623.
(b) You must submit the standard operating procedures manual for
baghouses required by paragraph (a) of this section to the
Administrator or delegated authority for review and approval.
(c) Unless the baghouse is equipped with a bag leak detection
system or CEMS, the procedures that you specify in the standard
operating procedures manual for inspections and routine maintenance
must, at a minimum,
[[Page 37395]]
include the requirements of paragraphs (c)(1) and (2) of this section.
(1) You must observe the baghouse outlet on a daily basis for the
presence of any visible emissions.
(2) In addition to the daily visible emissions observation, you
must conduct the following activities:
(i) Weekly confirmation that dust is being removed from hoppers
through visual inspection, or equivalent means of ensuring the proper
functioning of removal mechanisms.
(ii) Daily check of compressed air supply for pulse-jet baghouses.
(iii) An appropriate methodology for monitoring cleaning cycles to
ensure proper operation.
(iv) Monthly check of bag cleaning mechanisms for proper
functioning through visual inspection or equivalent means.
(v) Quarterly visual check of bag tension on reverse air and
shaker-type baghouses to ensure that the bags are not kinked (kneed or
bent) or lying on their sides. Such checks are not required for shaker-
type baghouses using self-tensioning (spring loaded) devices.
(vi) Quarterly confirmation of the physical integrity of the
baghouse structure through visual inspection of the baghouse interior
for air leaks.
(vii) Semiannual inspection of fans for wear, material buildup and
corrosion through visual inspection, vibration detectors, or equivalent
means.
(d) Bag leak detection system. (1) For each baghouse used to
control emissions from an electric arc furnace, you must install,
operate and maintain a bag leak detection system according to
paragraphs (d)(2) through (4) of this section, unless a system meeting
the requirements of paragraph (o) of this section, for a CEMS and
continuous emissions rate monitoring system, is installed for
monitoring the concentration of particulate matter. You may choose to
install, operate and maintain a bag leak detection system for any other
baghouse in operation at the facility according to paragraphs (d)(2)
through (4) of this section.
(2) The procedures you specified in the standard operating
procedures manual for baghouse maintenance must include, at a minimum,
a preventative maintenance schedule that is consistent with the
baghouse manufacturer's instructions for routine and long-term
maintenance.
(3) Each bag leak detection system must meet the specifications and
requirements in paragraphs (d)(3)(i) through (viii) of this section.
(i) The bag leak detection system must be certified by the
manufacturer to be capable of detecting PM emissions at concentrations
of 1.0 milligram per dry standard cubic meter (0.00044 grains per
actual cubic foot) or less.
(ii) The bag leak detection system sensor must provide output of
relative PM loadings.
(iii) The bag leak detection system must be equipped with an alarm
system that will alarm when an increase in relative particulate
loadings is detected over a preset level.
(iv) You must install and operate the bag leak detection system in
a manner consistent with the guidance provided in ``Office of Air
Quality Planning and Standards (OAQPS) Fabric Filter Bag Leak Detection
Guidance'' EPA-454/R-98-015, September 1997 (incorporated by reference,
see Sec. 63.14) and the manufacturer's written specifications and
recommendations for installation, operation and adjustment of the
system.
(v) The initial adjustment of the system must, at a minimum,
consist of establishing the baseline output by adjusting the
sensitivity (range) and the averaging period of the device and
establishing the alarm set points and the alarm delay time.
(vi) Following initial adjustment, you must not adjust the
sensitivity or range, averaging period, alarm set points, or alarm
delay time, except as detailed in the approved standard operating
procedures manual required under paragraph (a) of this section. You
cannot increase the sensitivity by more than 100 percent or decrease
the sensitivity by more than 50 percent over a 365-day period unless
such adjustment follows a complete baghouse inspection that
demonstrates that the baghouse is in good operating condition.
(vii) You must install the bag leak detector downstream of the
baghouse.
(viii) Where multiple detectors are required, the system's
instrumentation and alarm may be shared among detectors.
(4) You must include in the standard operating procedures manual
required by paragraph (a) of this section a corrective action plan that
specifies the procedures to be followed in the case of a bag leak
detection system alarm. The corrective action plan must include, at a
minimum, the procedures that you will use to determine and record the
time and cause of the alarm as well as the corrective actions taken to
minimize emissions as specified in paragraphs (d)(4)(i) and (ii) of
this section.
(i) The procedures used to determine the cause of the alarm must be
initiated within 30 minutes of the alarm.
(ii) The cause of the alarm must be alleviated by taking the
necessary corrective action(s) that may include, but not be limited to,
those listed in paragraphs (d)(4)(ii)(A) through (F) of this section.
(A) Inspecting the baghouse for air leaks, torn or broken filter
elements, or any other malfunction that may cause an increase in
emissions.
(B) Sealing off defective bags or filter media.
(C) Replacing defective bags or filter media, or otherwise
repairing the control device.
(D) Sealing off a defective baghouse compartment.
(E) Cleaning the bag leak detection system probe, or otherwise
repairing the bag leak detection system.
(F) Shutting down the process producing the particulate emissions.
(e) If you use a wet particulate matter scrubber, you must collect
the pressure drop and liquid flow rate monitoring system data according
to Sec. 63.1628, reduce the data to 24-hour block averages and
maintain the 24-hour average pressure drop and liquid flow-rate at or
above the operating limits established during the performance test
according to Sec. 63.1625(c)(4)(i).
(f) If you use curtains or partitions to prevent process fugitive
emissions from escaping the area around the process fugitive emission
source or other parts of the building, you must perform quarterly
inspections of the physical condition of these curtains or partitions
to determine if there are any tears or openings.
(g) Shop building opacity. In order to demonstrate continuous
compliance with the opacity standards in Sec. 63.1623, you must comply
with the requirements Sec. 63.1625(d)(1) and one of the monitoring
options in paragraphs (g)(1) or (2) of this section. The selected
option must be consistent with that selected during the initial
performance test described in Sec. 63.1625(d)(2). Alternatively, you
may use the provisions of Sec. 63.8(f) to request approval to use an
alternative monitoring method.
(1) If you choose to establish operating parameters during the
compliance test as specified in Sec. 63.1625(d)(2)(i), you must meet
one of the following requirements.
(i) Check and record the control system fan motor amperes and
capture system damper positions once per shift.
(ii) Install, calibrate and maintain a monitoring device that
continuously records the volumetric flow rate through each separately
ducted hood.
(iii) Install, calibrate and maintain a monitoring device that
continuously records the volumetric flow rate at the inlet of the air
pollution control device and check and record the capture system damper
positions once per shift.
[[Page 37396]]
(2) If you choose to establish operating parameters during the
compliance test as specified in Sec. 63.1625(d)(2)(ii), you must
monitor the selected parameter(s) on a frequency specified in the
assessment and according to a method specified in the engineering
assessment
(3) All flow rate monitoring devices must meet the following
requirements:
(i) Be installed in an appropriate location in the exhaust duct
such that reproducible flow rate monitoring will result.
(ii) Have an accuracy 10 percent over its normal
operating range and be calibrated according to the manufacturer's
instructions.
(4) The Administrator may require you to demonstrate the accuracy
of the monitoring device(s) relative to Methods 1 and 2 of appendix A-1
of part 60 of this chapter.
(5) Failure to maintain the appropriate capture system parameters
(e.g., fan motor amperes, flow rate and/or damper positions)
establishes the need to initiate corrective action as soon as
practicable after the monitoring excursion in order to minimize excess
emissions.
(h) Furnace capture system. You must perform quarterly (once every
three months) inspections of the furnace fugitive capture system
equipment to ensure that the hood locations have not been changed or
obstructed because of contact with cranes or ladles, quarterly
inspections of the physical condition of hoods and ductwork to the
control device to determine if there are any openings or leaks in the
ductwork, quarterly inspections of the hoods and ductwork to determine
if there are any flow constrictions in ductwork due to dents or
accumulated dust and quarterly examinations of the operational status
of flow rate controllers (pressure sensors, dampers, damper switches,
etc.) to ensure they are operating correctly. Any deficiencies must be
recorded and proper maintenance and repairs performed.
(i) Requirements for sources using CMS. If you demonstrate
compliance with any applicable emissions limit through use of a
continuous monitoring system (CMS), where a CMS includes a continuous
parameter monitoring system (CPMS) as well as a continuous emissions
monitoring system (CEMS), you must develop a site-specific monitoring
plan and submit this site-specific monitoring plan, if requested, at
least 60 days before your initial performance evaluation (where
applicable) of your CMS. Your site-specific monitoring plan must
address the monitoring system design, data collection and the quality
assurance and quality control elements outlined in this paragraph and
in Sec. 63.8(d). You must install, operate and maintain each CMS
according to the procedures in your approved site-specific monitoring
plan. Using the process described in Sec. 63.8(f)(4), you may request
approval of monitoring system quality assurance and quality control
procedures alternative to those specified in paragraphs (i)(1) through
(6) of this section in your site-specific monitoring plan.
(1) The performance criteria and design specifications for the
monitoring system equipment, including the sample interface, detector
signal analyzer and data acquisition and calculations;
(2) Sampling interface location such that the monitoring system
will provide representative measurements;
(3) Equipment performance checks, system accuracy audits, or other
audit procedures;
(4) Ongoing operation and maintenance procedures in accordance with
the general requirements of Sec. 63.8(c)(1) and (3);
(5) Conditions that define a continuous monitoring system that is
out of control consistent with Sec. 63.8(c)(7)(i) and for responding
to out of control periods consistent with Sec. 63.8(c)(7)(ii) and
(c)(8) or Table 1 to this subpart, as applicable; and
(6) Ongoing recordkeeping and reporting procedures in accordance
with provisions in Sec. 63.10(c), (e)(1) and (e)(2)(i), and Table 1 to
this subpart, as applicable.
(j) If you have an operating limit that requires the use of a CPMS,
you must install, operate and maintain each continuous parameter
monitoring system according to the procedures in paragraphs (j)(1)
through (7) of this section.
(1) The CPMS must complete a minimum of one cycle of operation for
each successive 15-minute period. You must have a minimum of four
successive cycles of operation to have a valid hour of data.
(2) Except for periods of monitoring system malfunctions, repairs
associated with monitoring system malfunctions and required monitoring
system quality assurance or quality control activities (including, as
applicable, system accuracy audits and required zero and span
adjustments), you must operate the CMS at all times the affected source
is operating. A monitoring system malfunction is any sudden,
infrequent, not reasonably preventable failure of the monitoring system
to provide valid data. Monitoring system failures that are caused in
part by poor maintenance or careless operation are not malfunctions.
You are required to complete monitoring system repairs in response to
monitoring system malfunctions and to return the monitoring system to
operation as expeditiously as practicable.
(3) You may not use data recorded during monitoring system
malfunctions, repairs associated with monitoring system malfunctions,
or required monitoring system quality assurance or control activities
in calculations used to report emissions or operating levels. You must
use all the data collected during all other required data collection
periods in assessing the operation of the control device and associated
control system.
(4) Except for periods of monitoring system malfunctions, repairs
associated with monitoring system malfunctions and required quality
monitoring system quality assurance or quality control activities
(including, as applicable, system accuracy audits and required zero and
span adjustments), failure to collect required data is a deviation of
the monitoring requirements.
(5) You must conduct other CPMS equipment performance checks,
system accuracy audits, or other audit procedures specified in your
site-specific monitoring plan at least once every 12 months.
(6) You must conduct a performance evaluation of each CPMS in
accordance with your site-specific monitoring plan.
(7) You must record the results of each inspection, calibration and
validation check.
(k) CPMS for measuring gaseous flow. (1) Use a flow sensor with a
measurement sensitivity of 5 percent of the flow rate or 10 cubic feet
per minute, whichever is greater;
(2) Check all mechanical connections for leakage at least every
month; and
(3) Perform a visual inspection at least every 3 months of all
components of the flow CPMS for physical and operational integrity and
all electrical connections for oxidation and galvanic corrosion if your
flow CPMS is not equipped with a redundant flow sensor.
(l) CPMS for measuring liquid flow. (1) Use a flow sensor with a
measurement sensitivity of 2 percent of the liquid flow rate; and
(2) Reduce swirling flow or abnormal velocity distributions due to
upstream and downstream disturbances.
(m) CPMS for measuring pressure. (1) Minimize or eliminate
pulsating pressure, vibration and internal and external corrosion; and
(2) Use a gauge with a minimum tolerance of 1.27 centimeters of
water or
[[Page 37397]]
a transducer with a minimum tolerance of 1 percent of the pressure
range.
(3) Perform checks at least once each process operating day to
ensure pressure measurements are not obstructed (e.g., check for
pressure tap pluggage daily).
(n) CPMS for measuring pH. (1) Ensure the sample is properly mixed
and representative of the fluid to be measured.
(2) Check the pH meter's calibration on at least two points every
eight hours of process operation.
(o) Particulate Matter CEMS. If you are using a CEMS to measure
particulate matter emissions to meet requirements of this subpart, you
must install, certify, operate and maintain the particulate matter CEMS
as specified in paragraphs (o)(1) through (4) of this section.
(1) You must conduct a performance evaluation of the PM CEMS
according to the applicable requirements of Sec. 60.13 of this chapter
and Performance Specification 11 at 40 CFR part 60, appendix B.
(2) During each PM correlation testing run of the CEMS required by
Performance Specification 11 at 40 CFR part 60, appendix B, PM and
oxygen (or carbon dioxide) collect data concurrently (or within a 30-
to 60-minute period) by both the CEMS and by conducting performance
tests using Method 5 or 5D at 40 CFR part 60, appendix A-3 or Method 17
at 40 CFR part 60, appendix A-6.
(3) Perform quarterly accuracy determinations and daily calibration
drift tests in accordance with Procedure 2 at 40 CFR part 60, appendix
F. Relative Response Audits must be performed annually and Response
Correlation Audits must be performed every 3 years.
(4) Within 60 days after the date of completing each CEMS relative
accuracy test audit or performance test conducted to demonstrate
compliance with this subpart, you must submit the relative accuracy
test audit data and the results of the performance test as specified in
Sec. 63.1628(e).
Sec. 63.1627 What notification requirements must I meet?
(a) You must comply with all of the notification requirements of
Sec. 63.9. Electronic notifications are encouraged when possible.
(b)(1) You must submit the process fugitive ventilation plan
required under Sec. 63.1624(a), the outdoor fugitive dust control plan
required under Sec. 63.1624(b), the site-specific monitoring plan for
CMS required under Sec. 63.1626(i) and the standard operating
procedures manual for baghouses required under Sec. 63.1626(a) to the
Administrator or delegated authority. You must submit this notification
no later than June 30, 2016. For sources that commenced construction or
reconstruction after June 30, 2015, you must submit this notification
no later than 180 days before startup of the constructed or
reconstructed ferromanganese or silicomanganese production facility.
For an affected source that has received a construction permit from the
Administrator or delegated authority on or before June 30, 2015, you
must submit this notification no later than June 30, 2016.
(2) The plans and procedures documents submitted as required under
paragraph (b)(1) of this section must be submitted to the Administrator
in electronic format and whenever an update is made to the procedure.
Sec. 63.1628 What recordkeeping and reporting requirements must I
meet?
(a) You must comply with all of the recordkeeping and reporting
requirements specified in Sec. 63.10 of the General Provisions that
are referenced in Table 1 to this subpart.
(1) Records must be maintained in a form suitable and readily
available for expeditious review, according to Sec. 63.10(b)(1).
However, electronic recordkeeping and reporting is encouraged and
required for some records and reports.
(2) Records must be kept on site for at least 2 years after the
date of occurrence, measurement, maintenance, corrective action,
report, or record, according to Sec. 63.10(b)(1).
(b) You must maintain, for a period of 5 years, records of the
information listed in paragraphs (b)(1) through (11) of this section.
(1) Electronic records of the bag leak detection system output.
(2) An identification of the date and time of all bag leak
detection system alarms, the time that procedures to determine the
cause of the alarm were initiated, the cause of the alarm, an
explanation of the corrective actions taken and the date and time the
cause of the alarm was corrected.
(3) All records of inspections and maintenance activities required
under Sec. 63.1626(c) as part of the practices described in the
standard operating procedures manual for baghouses required under Sec.
63.1626(a).
(4) Electronic records of the pressure drop and water flow rate
values for wet scrubbers used to control particulate matter emissions
as required in Sec. 63.1626(e), identification of periods when the 1-
hour average pressure drop and water flow rate values are below the
established minimum operating limits and an explanation of the
corrective actions taken.
(5) Electronic records of the shop building capture system
monitoring required under Sec. 63.1626(g)(1) and (2), as applicable,
or identification of periods when the capture system parameters were
not maintained and an explanation of the corrective actions taken.
(6) Records of the results of quarterly inspections of the furnace
capture system required under Sec. 63.1626(h).
(7) Electronic records of the continuous flow monitors or pressure
monitors required under Sec. 63.1626(i) and (j) and an identification
of periods when the flow rate or pressure was not maintained as
required in Sec. 63.1626(e).
(8) Electronic records of the output of any CEMS installed to
monitor particulate matter emissions meeting the requirements of Sec.
63.1626(i).
(9) Records of the occurrence and duration of each startup and/or
shutdown.
(10) Records of the occurrence and duration of each malfunction of
operation (i.e., process equipment) or the air pollution control
equipment and monitoring equipment.
(11) Records that explain the periods when the procedures outlined
in the process fugitives ventilation plan required under Sec.
63.1624(a), the fugitives dust control plan required under Sec.
63.1624(b), the site-specific monitoring plan for CMS required under
Sec. 63.1626(i) and the standard operating procedures manual for
baghouses required under Sec. 63.1626(a).
(c) You must comply with all of the reporting requirements
specified in Sec. 63.10 of the General Provisions that are referenced
in Table 1 to this subpart.
(1) You must submit reports no less frequently than specified under
Sec. 63.10(e)(3) of the General Provisions.
(2) Once a source reports a violation of the standard or excess
emissions, you must follow the reporting format required under Sec.
63.10(e)(3) until a request to reduce reporting frequency is approved
by the Administrator.
(d) In addition to the information required under the applicable
sections of Sec. 63.10, you must include in the reports required under
paragraph (c) of this section the information specified in paragraphs
(d)(1) through (7) of this section.
(1) Reports that identify and explain the periods when the
procedures outlined in the process fugitives ventilation plan required
under Sec. 63.1624(a), the fugitives dust control plan required under
Sec. 63.1624(b), the site-specific monitoring plan for CMS required
under Sec. 63.1626(i) and the
[[Page 37398]]
standard operating procedures manual for baghouses required under Sec.
63.1626(a) were not followed.
(2) Reports that identify the periods when the average hourly
pressure drop or flow rate of wet scrubbers used to control particulate
emissions dropped below the levels established in Sec. 63.1626(e) and
an explanation of the corrective actions taken.
(3) Bag leak detection system. Reports including the following
information:
(i) Records of all alarms.
(ii) Description of the actions taken following each bag leak
detection system alarm.
(4) Reports of the shop building capture system monitoring required
under Sec. 63.1626(g)(1) and (2), as applicable, identification of
periods when the capture system parameters were not maintained and an
explanation of the corrective actions taken.
(5) Reports of the results of quarterly inspections of the furnace
capture system required under Sec. 63.1626(h).
(6) Reports of the CPMS required under Sec. 63.1626, an
identification of periods when the monitored parameters were not
maintained as required in Sec. 63.1626 and corrective actions taken.
(7) If a malfunction occurred during the reporting period, the
report must include the number, duration and a brief description for
each type of malfunction that occurred during the reporting period and
caused or may have caused any applicable emissions limitation to be
exceeded. The report must also include a description of actions taken
by the owner or operator during a malfunction of an affected source to
minimize emissions in accordance with Sec. 63.1623(f), including
actions taken to correct a malfunction.
(e) Within 60 days after the date of completing each CEMS relative
accuracy test audit or performance test conducted to demonstrate
compliance with this subpart, you must submit the relative accuracy
test audit data and the results of the performance test in the method
specified by paragraphs (e)(1) and (2) of this section. The results of
the performance test must contain the information listed in paragraph
(e)(2) of this section.
(1)(i) Within 60 days after the date of completing each performance
test (as defined in Sec. 63.2) required by this subpart, you must
submit the results of the performance tests, including any associated
fuel analyses, following the procedure specified in either paragraph
(e)(1)(i)(A) or (B) of this section.
(A) For data collected using test methods supported by the EPA's
Electronic Reporting Tool (ERT) as listed on the EPA's ERT Web site
(https://www.epa.gov/ttn/chief/ert/), you must submit the
results of the performance test to the EPA via the Compliance and
Emissions Data Reporting Interface (CEDRI). CEDRI can be accessed
through the EPA's Central Data Exchange (CDX) (https://cdx.epa.gov/epa_home.asp). Performance test data must be submitted in a file format
generated through the use of the EPA's ERT. Alternatively, you may
submit performance test data in an electronic file format consistent
with the extensible markup language (XML) schema listed on the EPA's
ERT Web site once the XML schema is available. If you claim that some
of the performance test information being submitted is confidential
business information (CBI), you must submit a complete file generated
through the use of the EPA's ERT or an alternate electronic file
consistent with the XML schema listed on the EPA's ERT Web site,
including information claimed to be CBI, on a compact disk, flash
drive, or other commonly used electronic storage media to the EPA. The
electronic media must be clearly marked as CBI and mailed to U.S. EPA/
OAQPS/CORE CBI Office, Attention: Group Leader, Measurement Policy
Group, MD C404-02, 4930 Old Page Rd., Durham, NC 27703. The same ERT or
alternate file with the CBI omitted must be submitted to the EPA via
the EPA's CDX as described earlier in this paragraph (e)(1)(i)(A).
(B) For data collected using test methods that are not supported by
the EPA's ERT as listed on the EPA's ERT Web site, you must submit the
results of the performance test to the Administrator at the appropriate
address listed in Sec. 63.13.
(ii) Within 60 days after the date of completing each CEMS
performance evaluation (as defined in Sec. 63.2), you must submit the
results of the performance evaluation following the procedure specified
in either paragraph (b)(1) or (2) of this section.
(A) For performance evaluations of continuous monitoring systems
measuring relative accuracy test audit (RATA) pollutants that are
supported by the EPA's ERT as listed on the EPA's ERT Web site, you
must submit the results of the performance evaluation to the EPA via
the CEDRI. (CEDRI can be accessed through the EPA's CDX.) Performance
evaluation data must be submitted in a file format generated through
the use of the EPA's ERT. Alternatively, you may submit performance
evaluation data in an electronic file format consistent with the XML
schema listed on the EPA's ERT Web site, once the XML schema is
available. If you claim that some of the performance evaluation
information being transmitted is CBI, you must submit a complete file
generated through the use of the EPA's ERT or an alternative electronic
file consistent with the XML schema listed on the EPA's ERT Web site,
including information claimed to be CBI, on a compact disk, flash drive
or other commonly used electronic storage media to the EPA. The
electronic storage media must be clearly marked as CBI and mailed to
U.S. EPA/OAQPS/CORE CBI Office, Attention: Group Leader, Measurement
Policy Group, MD C404-02, 4930 Old Page Rd., Durham, NC 27703. The same
ERT file or alternate file with the CBI omitted must be submitted to
the EPA via the EPA's CDX as described earlier in this paragraph
(e)(1)(ii)(A).
(B) For any performance evaluations of continuous monitoring
systems measuring RATA pollutants that are not supported by the EPA's
ERT as listed on the EPA's ERT Web site, you must submit the results of
the performance evaluation to the Administrator at the appropriate
address listed in Sec. 63.13.
(2) The results of a performance test shall include the purpose of
the test; a brief process description; a complete unit description,
including a description of feed streams and control devices; sampling
site description; pollutants measured; description of sampling and
analysis procedures and any modifications to standard procedures;
quality assurance procedures; record of operating conditions, including
operating parameters for which limits are being set, during the test;
record of preparation of standards; record of calibrations; raw data
sheets for field sampling; raw data sheets for field and laboratory
analyses; chain-of-custody documentation; explanation of laboratory
data qualifiers; example calculations of all applicable stack gas
parameters, emission rates, percent reduction rates and analytical
results, as applicable; and any other information required by the test
method, a relevant standard, or the Administrator.
Sec. 63.1629 Who implements and enforces this subpart?
(a) This subpart can be implemented and enforced by the U.S. EPA,
or a delegated authority such as the applicable state, local, or tribal
agency. If the U.S. EPA Administrator has delegated authority to a
state, local, or tribal agency, then that agency, in addition to the
U.S. EPA, has the authority to implement and enforce this subpart.
Contact the applicable U.S. EPA Regional Office to find out if this
[[Page 37399]]
subpart is delegated to a state, local, or tribal agency.
(b) In delegating implementation and enforcement authority of this
subpart to a state, local, or tribal agency under subpart E of this
part, the authorities contained in paragraph (c) of this section are
retained by the Administrator of U.S. EPA and cannot be transferred to
the state, local, or tribal agency.
(c) The authorities that cannot be delegated to state, local, or
tribal agencies are as specified in paragraphs (c)(1) through (4) of
this section.
(1) Approval of alternatives to requirements in Sec. Sec. 63.1620
and 63.1621 and 63.1623 and 63.1624.
(2) Approval of major alternatives to test methods under Sec.
63.7(e)(2)(ii) and (f), as defined in Sec. 63.90 and as required in
this subpart.
(3) Approval of major alternatives to monitoring under Sec.
63.8(f), as defined in Sec. 63.90 and as required in this subpart.
(4) Approval of major alternatives to recordkeeping and reporting
under Sec. 63.10(f), as defined in Sec. 63.90 and as required in this
subpart.
0
4. Section 63.1650 is amended by:
0
a. Revising paragraph (d);
0
b. Removing and reserving paragraph (e)(1); and
0
c. Revising paragraph (e)(2).
The revisions read as follows:
Sec. 63.1650 Applicability and compliance dates.
* * * * *
(d) Table 1 to this subpart specifies the provisions of subpart A
of this part that apply to owners and operators of ferroalloy
production facilities subject to this subpart.
(e) * * *
(2) Each owner or operator of a new or reconstructed affected
source that commences construction or reconstruction after August 4,
1998 and before November 23, 2011, must comply with the requirements of
this subpart by May 20, 1999 or upon startup of operations, whichever
is later.
0
5. Section 63.1652 is amended by adding paragraph (f) to read as
follows:
Sec. 63.1652 Emission standards.
* * * * *
(f) At all times, you must operate and maintain any affected
source, including associated air pollution control equipment and
monitoring equipment, in a manner consistent with safety and good air
pollution control practices for minimizing emissions. Determination of
whether such operation and maintenance procedures are being used will
be based on information available to the Administrator that may
include, but is not limited to, monitoring results, review of operation
and maintenance procedures, review of operation and maintenance records
and inspection of the source.
0
6. Section 63.1656 is amended by:
0
a. Adding paragraph (a)(6);
0
b. Revising paragraphs (b)(7) and (e)(1); and
0
c. Removing and reserving paragraph (e)(2)(ii).
The addition and revisions read as follows:
Sec. 63.1656 Performance testing, test methods, and compliance
demonstrations.
(a) * * *
(6) You must conduct the performance tests specified in paragraph
(c) of this section under such conditions as the Administrator
specifies based on representative performance of the affected source
for the period being tested. Upon request, you must make available to
the Administrator such records as may be necessary to determine the
conditions of performance tests.
(b) * * *
(7) Method 9 of appendix A-4 of 40 CFR part 60 to determine
opacity. ASTM D7520-13, ``Standard Test Method for Determining the
Opacity of a Plume in the Outdoor Ambient Atmosphere'' may be used
(incorporated by reference, see Sec. 63.14) with the following
conditions:
(i) During the digital camera opacity technique (DCOT)
certification procedure outlined in Section 9.2 of ASTM D7520-13, the
owner or operator or the DCOT vendor must present the plumes in front
of various backgrounds of color and contrast representing conditions
anticipated during field use such as blue sky, trees and mixed
backgrounds (clouds and/or a sparse tree stand).
(ii) The owner or operator must also have standard operating
procedures in place including daily or other frequency quality checks
to ensure the equipment is within manufacturing specifications as
outlined in Section 8.1 of ASTM D7520-13.
(iii) The owner or operator must follow the recordkeeping
procedures outlined in Sec. 63.10(b)(1) for the DCOT certification,
compliance report, data sheets and all raw unaltered JPEGs used for
opacity and certification determination.
(iv) The owner or operator or the DCOT vendor must have a minimum
of four (4) independent technology users apply the software to
determine the visible opacity of the 300 certification plumes. For each
set of 25 plumes, the user may not exceed 15 percent opacity of any one
reading and the average error must not exceed 7.5 percent opacity.
(v) Use of this approved alternative does not provide or imply a
certification or validation of any vendor's hardware or software. The
onus to maintain and verify the certification and/or training of the
DCOT camera, software and operator in accordance with ASTM D7520-13 and
these requirements is on the facility, DCOT operator and DCOT vendor.
* * * * *
(e) * * *
(1) Fugitive dust sources. Failure to have a fugitive dust control
plan or failure to report deviations from the plan and take necessary
corrective action would be a violation of the general duty to ensure
that fugitive dust sources are operated and maintained in a manner
consistent with good air pollution control practices for minimizing
emissions per Sec. 63.1652(f).
* * * * *
0
7. Section 63.1657 is amended by revising paragraphs (a)(6), (b)(3),
and (c)(7) to read as follows:
Sec. 63.1657 Monitoring requirements.
(a) * * *
(6) Failure to monitor or failure to take corrective action under
the requirements of paragraph (a) of this section would be a violation
of the general duty to operate in a manner consistent with good air
pollution control practices that minimizes emissions per Sec.
63.1652(f).
(b) * * *
(3) Failure to monitor or failure to take corrective action under
the requirements of paragraph (b) of this section would be a violation
of the general duty to operate in a manner consistent with good air
pollution control practices that minimizes emissions per Sec.
63.1652(f).
(c) * * *
(7) Failure to monitor or failure to take corrective action under
the requirements of paragraph (c) of this section would be a violation
of the general duty to operate in a manner consistent with good air
pollution control practices that minimizes emissions per Sec.
63.1652(f).
0
8. Section 63.1659 is amended by revising paragraph (a)(4) to read as
follows:
Sec. 63.1659 Reporting requirements.
(a) * * *
(4) Reporting malfunctions. If a malfunction occurred during the
reporting period, the report must include the number, duration and a
brief description for each type of
[[Page 37400]]
malfunction which occurred during the reporting period and which caused
or may have caused any applicable emission limitation to be exceeded.
The report must also include a description of actions taken by an owner
or operator during a malfunction of an affected source to minimize
emissions in accordance with Sec. 63.1652(f), including actions taken
to correct a malfunction.
* * * * *
0
9. Section 63.1660 is amended by:
0
a. Revising paragraphs (a)(2)(i) and (ii); and
0
b. Removing and reserving paragraphs (a)(2)(iv) and (v).
The revisions read as follows:
Sec. 63.1660 Recordkeeping requirements.
(a) * * *
(2) * * *
(i) Records of the occurrence and duration of each malfunction of
operation (i.e., process equipment) or the air pollution control
equipment and monitoring equipment;
(ii) Records of actions taken during periods of malfunction to
minimize emissions in accordance with Sec. 63.1652(f), including
corrective actions to restore malfunctioning process and air pollution
control and monitoring equipment to its normal or usual manner of
operation;
* * * * *
0
10. Add Table 1 to the end of subpart XXX to read as follows:
Table 1--to Subpart XXX of Part 63--General Provisions Applicability to
Subpart XXX
------------------------------------------------------------------------
Applies to
Reference subpart XXX Comment
------------------------------------------------------------------------
Sec. 63.1................... Yes.............. .....................
Sec. 63.2................... Yes.............. .....................
Sec. 63.3................... Yes.............. .....................
Sec. 63.4................... Yes.............. .....................
Sec. 63.5................... Yes.............. .....................
Sec. 63.6(a), (b), (c)...... Yes.............. .....................
Sec. 63.6(d)................ No............... Section reserved.
Sec. 63.6(e)(1)(i).......... No............... See Sec. Sec.
63.1623(g) and
63.1652(f) for
general duty
requirement.
Sec. 63.6(e)(1)(ii)......... No............... .....................
Sec. 63.6(e)(1)(iii)........ Yes.............. .....................
Sec. 63.6(e)(2)............. No............... Section reserved.
Sec. 63.6(e)(3)............. No............... .....................
Sec. 63.6(f)(1)............. No............... .....................
Sec. 63.6(f)(2)-(3)......... Yes.............. .....................
Sec. 63.6(g)................ Yes.............. .....................
Sec. 63.6(h)(1)............. No............... .....................
Sec. 63.6(h)(2)-(9)......... Yes.............. .....................
Sec. 63.6(i)................ Yes.............. .....................
Sec. 63.6(j)................ Yes.............. .....................
Sec. 63.7(a)-(d)............ Yes.............. .....................
Sec. 63.7(e)(1)............. No............... See Sec. Sec.
63.1625(a)(5) and
63.1656(a)(6).
Sec. 63.7(e)(2)-(4)......... Yes.............. .....................
Sec. 63.7(f), (g), (h)...... Yes.............. .....................
Sec. 63.8(a)-(b)............ Yes.............. .....................
Sec. 63.8(c)(1)(i).......... No............... See Sec. Sec.
63.1623(g) and
63.1652(f) for
general duty
requirement.
Sec. 63.8(c)(1)(ii)......... Yes.............. .....................
Sec. 63.8(c)(1)(iii)........ No............... .....................
Sec. 63.8(c)(2)-(d)(2)...... Yes.............. .....................
Sec. 63.8(d)(3)............. Yes, except for SSM plans are not
last sentence. required.
Sec. 63.8(e)-(g)............ Yes.............. .....................
Sec. Yes.............. .....................
63.9(a),(b),(c),(e),(g),(h)(1
) through (3), (h)(5) and
(6), (i) and (j).
Sec. 63.9(f)................ Yes.............. .....................
Sec. 63.9(h)(4)............. No............... Section reserved.
Sec. 63.10(a)............... Yes.............. .....................
Sec. 63.10(b)(1)............ Yes.............. .....................
Sec. 63.10(b)(2)(i)......... No............... .....................
Sec. 63.10(b)(2)(ii)........ No............... See Sec. Sec.
63.1628 and 63.1660
for recordkeeping of
(1) occurrence and
duration and (2)
actions taken during
malfunction.
Sec. 63.10(b)(2)(iii)....... Yes.............. .....................
Sec. 63.10(b)(2)(iv)-(v).... No............... .....................
Sec. 63.10(b)(2)(vi)-(xiv).. Yes.............. .....................
Sec. 63.10)(b)(3)........... Yes.............. .....................
Sec. 63.10(c)(1)-(9)........ Yes.............. .....................
Sec. 63.10(c)(10)-(11)...... No............... See Sec. Sec.
63.1628 and 63.1660
for malfunction
recordkeeping
requirements.
Sec. 63.10(c)(12)-(14)...... Yes.............. .....................
Sec. 63.10(c)(15)........... No............... .....................
Sec. 63.10(d)(1)-(4)........ Yes.............. .....................
Sec. 63.10(d)(5)............ No............... See Sec. Sec.
63.1628(d)(8) and
63.1659(a)(4) for
malfunction
reporting
requirements.
Sec. 63.10(e)-(f)........... Yes.............. .....................
[[Page 37401]]
Sec. 63.11.................. No............... Flares will not be
used to comply with
the emission limits.
Sec. Sec. 63.12-63.15...... Yes.............. .....................
------------------------------------------------------------------------
[FR Doc. 2015-15038 Filed 6-29-15; 8:45 am]
BILLING CODE 6560-50-P