National Emission Standards for Hazardous Air Pollutants for Area Sources: Polyvinyl Chloride and Copolymers Production, Primary Copper Smelting, Secondary Copper Smelting, and Primary Nonferrous Metals-Zinc, Cadmium, and Beryllium, 59302-59334 [06-8434]
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Federal Register / Vol. 71, No. 194 / Friday, October 6, 2006 / Proposed Rules
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 63
[EPA–HQ–OAR–2006–0510; FRL–8226–8]
RIN 2060–AN45
National Emission Standards for
Hazardous Air Pollutants for Area
Sources: Polyvinyl Chloride and
Copolymers Production, Primary
Copper Smelting, Secondary Copper
Smelting, and Primary Nonferrous
Metals—Zinc, Cadmium, and Beryllium
Environmental Protection
Agency (EPA).
ACTION: Proposed rules.
AGENCY:
SUMMARY: EPA is proposing national
emission standards for hazardous air
pollutants (NESHAP) for four area
source categories. The proposed
NESHAP reflect EPA’s determination
that existing facilities in three of these
categories are well controlled and that
the emission control devices and work
practices at these facilities represent the
generally available control technology
(GACT) for these source categories. For
secondary copper smelting, we are
proposing NESHAP for new area
sources because there is not, and never
will be, any existing source in this
category.
Comments must be received on
or before November 6, 2006 unless a
public hearing is requested by October
16, 2006. If a hearing is requested on the
proposed rules, written comments must
be received by November 20, 2006.
Public Hearing. If anyone contacts
EPA requesting to speak at a public
hearing concerning the proposed rules
by October 16, 2006, we will hold a
public hearing on October 23, 2006. If
you are interested in attending the
public hearing, contact Ms. Pamela
Garrett at (919) 541–7966 to verify that
a hearing will be held.
ADDRESSES: Submit your comments,
identified by Docket ID No. EPA–HQ–
OAR–2006–0510, by one of the
following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the on-line
instructions for submitting comments.
• E-mail: a-and-r-docket@epa.gov.
• Fax: (202) 566–1741.
• Mail: National Emission Standards
for Hazardous Air Pollutants for Four
Area Source Categories, Docket No.
EPA–HQ–OAR–2006–0510,
Environmental Protection Agency, EPA
Docket Center, Mailcode 6102T, 1200
Pennsylvania Ave., NW., Washington,
DC 20460. Please include a total of two
copies. In addition, please mail a copy
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DATES:
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of your comments on the information
collection provisions to the Office of
Information and Regulatory Affairs,
Office of Management and Budget
(OMB), Attn: Desk Officer for EPA, 725
17th St., NW., Washington, DC 20503.
• Hand Delivery: EPA Docket Center,
Public Reading Room, EPA West, Room
B102, 1301 Constitution Ave., NW.,
Washington, DC 20460. Such deliveries
are only accepted during the Docket’s
normal hours of operation, and special
arrangements should be made for
deliveries of boxed information. Note:
The EPA Docket Center suffered damage
due to flooding during the last week of
June 2006. The Docket Center is
continuing to operate. However, during
the cleanup, there will be temporary
changes to Docket Center telephone
numbers, addresses, and hours of
operation for people who wish to make
hand deliveries or visit the Public
Reading Room to view documents.
Consult EPA’s Federal Register notice at
71 FR 38147 (July 5, 2006) or the EPA
Web site at https://www.epa.gov/
epahome/dockets.htm for current
information on docket operations,
locations and telephone numbers.
Instructions: Direct your comments to
Docket ID No. EPA–HQ–OAR–2006–
0510. EPA’s policy is that all comments
received will be included in the public
docket without change and may be
made available online at https://
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be confidential business
information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through www.regulations.gov
or e-mail. The www.regulations.gov Web
site is an ‘‘anonymous access’’ system,
which means EPA will not know your
identity or contact information unless
you provide it in the body of your
comment. If you send an e-mail
comment directly to EPA without going
through www.regulations.gov, your email address will be automatically
captured and included as part of the
comment that is placed in the public
docket and made available on the
Internet. If you submit an electronic
comment, EPA recommends that you
include your name and other contact
information in the body of your
comment and with any disk or CD–ROM
you submit. If EPA cannot read your
comment due to technical difficulties
and cannot contact you for clarification,
EPA may not be able to consider your
comment. Electronic files should avoid
the use of special characters, any form
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of encryption, and be free of any defects
or viruses.
Docket: All documents in the docket
are listed in the Federal Docket
Management System index at https://
www.regulations.gov. Although listed in
the index, some information is not
publicly available, e.g., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
is not placed on the Internet and will be
publicly available only in hard copy
form. Publicly available docket
materials are available either
electronically through
www.regulations.gov or in hard copy at
the EPA Docket Center, Public Reading
Room, EPA West, Room B102, 1301
Constitution Ave., NW., Washington,
DC. The Public Reading Room is open
from 8:30 a.m. to 4:30 p.m., Monday
through Friday, excluding legal
holidays. The telephone number for the
Public Reading Room is (202) 566–1744,
and the telephone number for the Air
Docket is (202) 566–1742.
Mr.
Bob Schell, U.S. EPA, Office of Air
Quality Planning and Standards, Sector
Policies and Programs Division, Metals
and Minerals Group (D243–02),
Research Triangle Park, North Carolina
27711, telephone number: (919) 541–
4116, fax number (919) 541–3207, email address: schell.bob@epa.gov.
FOR FURTHER INFORMATION CONTACT:
Outline.
The information presented in this
preamble is organized as follows:
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does this action apply to me?
B. What should I consider as I prepare my
comments to EPA?
C. Where can I get a copy of this document
and other related information?
II. Background Information for Proposed Area
Source Standards
III. Proposed NESHAP for Polyvinyl Chloride
and Copolymers Production Area
Sources
A. What area source category is affected by
the proposed NESHAP?
B. What HAP are emitted from polyvinyl
chloride and copolymers production?
C. What are the proposed requirements for
area sources?
D. What is our rationale for selecting the
proposed standards for area sources?
E. What is our rationale for exempting
polyvinyl chloride and copolymers
production area sources from the CAA
title V permit requirements?
IV. Proposed NESHAP for Primary Copper
Smelting Area Sources
A. What area source category is affected by
the proposed NESHAP?
B. What HAP are emitted from primary
copper smelters?
C. What are the proposed requirements for
area sources?
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D. What is our rationale for selecting the
proposed standards for area sources?
V. Proposed NESHAP for Secondary Copper
Smelting Area Sources
A. What area source category is affected by
the proposed NESHAP?
B. What HAP are emitted from secondary
copper smelters?
C. What are the proposed requirements for
area sources?
D. What is our rationale for selecting the
proposed standards for area sources?
VI. Proposed NESHAP for Primary
Nonferrous Metals-Zinc, Cadmium, and
Beryllium Area Sources
A. What area source category is affected by
the proposed NESHAP?
B. What is primary zinc production and
what HAP are emitted?
C. What are the proposed requirements for
primary zinc production area sources?
D. What is our rationale for selecting the
proposed standards for primary zinc
production area sources?
E. What is primary beryllium production
and what HAP are emitted?
F. What are the proposed requirements for
primary beryllium production area
sources?
G. What is our rationale for selecting the
proposed standards for primary
beryllium production area sources?
VII. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory
Planning and Review
B. Paperwork Reduction Act
C. Regulatory Flexibility Act
D. Unfunded Mandates Reform Act
E. Executive Order 13132: Federalism
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F. Executive Order 13175: Consultation
and Coordination with Indian Tribal
Governments
G. Executive Order 13045: Protection of
Children from Environmental Health and
Safety Risks
H. Executive Order 13211: Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution, or Use
I. National Technology Transfer
Advancement Act
I. General Information
A. Does this action apply to me?
The regulated categories and entities
potentially affected by the proposed
standards include:
Category
NAICS
code 1
Examples of regulated entities
Industry:
Polyvinyl chloride and copolymers production.
Primary copper smelting .......................
325211
Area source facilities that polymerize and copolymers vinyl chloride monomer to
produce vinyl production chloride and/or copolymer products.
Area source facilities that produce copper from copper sulfide ore concentrates using
pyrometallurgical techniques.
Area source facilities that process smelting copper scrap in a blast furnace and converter or use another pyrometallurgical purification process to produce anode copper
from copper scrap, including low-grade copper scrap.
Area source facilities that produce zinc, zinc oxide, cadmium, or cadmium oxide from
zinc sulfide ore concentrates using pyrometallurgical techniques and area source facilities that produce beryllium metal, alloy, or oxide from beryllium ore.
Not affected.
Not affected.
331411
Secondary copper smelting ..................
331423 2
Primary nonferrous metals - zinc, cadmium, and beryllium.
331419
Federal government ..............................
State/local/tribal government ................
1 North
American Industry Classification System.
proposed rule applies only to secondary copper smelters and does not apply to copper, brass, and bronze ingot makers or remelters that
may also be included under this NAICS code. There are no existing secondary copper smelters as defined in the proposed rule.
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2 The
This table is not intended to be
exhaustive, but rather provides a guide
for readers regarding entities likely to be
affected by this action. To determine
whether your facility would be
regulated by this action, you should
examine the applicability criteria in 40
CFR 63.11140 of subpart DDDDDD
(NESHAP for Polyvinyl Chloride and
Copolymers Production Area Sources),
40 CFR 63.11146 of subpart EEEEEE
(NESHAP for Primary Copper Smelting
Area Sources), 40 CFR 63.11153 of
subpart FFFFFF (NESHAP for
Secondary Copper Smelting Area
Sources), or 40 CFR 63.11160 of subpart
GGGGGG (NESHAP for Primary
Nonferrous Metals—Zinc, Cadmium,
and Beryllium Area Sources). If you
have any questions regarding the
applicability of this action to a
particular entity, consult either the air
permit authority for the entity or your
EPA regional representative as listed in
40 CFR 63.13 of subpart A (General
Provisions).
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B. What should I consider as I prepare
my comments to EPA?
Do not submit information containing
CBI to EPA through
www.regulations.gov or e-mail. Send or
deliver information identified as CBI
only to the following address: Roberto
Morales, OAQPS Document Control
Officer (C404–02), U.S. EPA, Office of
Air Quality Planning and Standards,
Research Triangle Park, North Carolina
27711, Attention Docket ID EPA–HQ–
OAR–2006–0510. Clearly mark the part
or all of the information that you claim
to be CBI. For CBI information in a disk
or CD ROM that you mail to EPA, mark
the outside of the disk or CD ROM as
CBI and then identify electronically
within the disk or CD ROM the specific
information that is claimed as CBI. In
addition to one complete version of the
comment that includes information
claimed as CBI, a copy of the comment
that does not contain the information
claimed as CBI must be submitted for
inclusion in the public docket.
Information so marked will not be
disclosed except in accordance with
procedures set forth in 40 CFR part 2.
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C. 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 these
proposed actions will also be available
on the Worldwide Web (WWW) through
the Technology Transfer Network
(TTN). Following signature, a copy of
the proposed actions will be posted on
the TTN’s policy and guidance page for
newly proposed or promulgated rules at
the following address: https://
www.epa.gov/ttn/oarpg/. The TTN
provides information and technology
exchange in various areas of air
pollution control.
II. Background Information for
Proposed Area Source Standards
Section 112(d) of the Clean Air Act
(CAA) requires us to establish NESHAP
for both major and area sources of
hazardous air pollutants (HAP) that are
listed for regulation under CAA section
112(c). A major source is a stationary
source that emits or has the potential to
emit 10 tons per year (tpy) or more of
any HAP or 25 tpy or more of any
combination of HAP. An area source is
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a stationary source that is not a major
source (i.e., an area source does not emit
and does not have the potential to emit
either 10 tpy or more of any single HAP
or 25 tpy or more of any combination of
HAP).
Requirements for area sources are
described in CAA sections 112(c)(3) and
112(k). These provisions direct EPA (1)
to identify not less than 30 HAP that
present the threat to public health in the
largest number of urban areas and (2) to
identify sufficient area source categories
to ensure that sources representing 90
percent or more of the emissions of each
of the 30 ‘‘listed’’ HAP (‘‘urban HAP’’)
are subject to regulation. We
implemented these listing requirements
through the Integrated Urban Air Toxics
Strategy (64 FR 38715, July 19, 1999).1
However, EPA has not completed the
required regulatory action for all of the
listed area source categories. Pursuant to
CAA section 304, Sierra Club brought
suit in the district court for the District
of Columbia to compel EPA to complete
this action (Sierra Club v. U.S.
Environmental Protection Agency, no.
01–1537, DC Cir.). On March 31, 2006,
the court issued an order requiring,
among other things, that we complete
regulatory action for a specified number
of area source categories every 6 months
starting December 15, 2006, and
complete regulatory action of all
remaining categories by June 15, 2009.
The order requires that, by December
15, 2006, we complete regulatory action
for four area source categories. The four
area source categories that we have
selected to meet this obligation and are
therefore subject of this proposal are as
follows: (1) Primary Copper Smelting;
(2) Secondary Copper Smelting; (3)
Polyvinyl Chloride and Copolymers
Production; and (4) Primary Nonferrous
Metals—Zinc, Cadmium, and Beryllium.
On June 26, 2002, we amended the
area source category list by adding
additional source categories, including
Polyvinyl Chloride and Copolymers
Production, Secondary Copper
Smelting, and Cadmium Refining and
Cadmium Oxide Production source
categories (67 FR 43112, 43113). On
November 22, 2002, we further
amended the category list by, among
other things, adding Primary Copper
Smelting (67 FR 70427, 70428). We also
expanded the Cadmium Refining and
Cadmium Oxide Production source
category to include primary zinc and
beryllium production and renamed the
category accordingly as Primary
1Since its publication in the Integrated Urban Air
Toxics Strategy in 1999, the area source category
list has undergone several amendments.
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Nonferrous Metals—Zinc, Cadmium,
and Beryllium.
The inclusion of each of the four
source categories on the area source
category list is based on data from the
CAA section 112(k) inventory, which
represents 1990 urban air data. The
Polyvinyl Chloride and Copolymers
Production source category listing was
based on vinyl chloride emissions. The
Primary Copper Smelting source
category listing was based on HAP metal
emissions (arsenic, cadmium,
chromium, lead, and nickel), while
Secondary Copper Smelting was based
on HAP emissions of cadmium, lead,
and dioxin. The listing of the Primary
Nonferrous Metals-Zinc, Cadmium, and
Beryllium source category was based on
emissions of arsenic, cadmium, lead,
manganese, and nickel.
Section 112(k)(3)(B) of the CAA
requires that EPA ensure that sources
representing 90 percent of the emissions
of each of the 30 urban HAP are subject
to standards pursuant to section 112(d).
Under CAA section 112(d)(5), the
Administrator may, in lieu of standards
requiring maximum achievable control
technology (MACT) under section
112(d)(2), elect to promulgate standards
or requirements for area sources ‘‘which
provide for the use of generally
available control technologies [‘‘GACT’’]
or management practices by such
sources to reduce emissions of
hazardous air pollutants.’’ Under
section 112(d)(5), the Administrator has
the discretion to use GACT in lieu of
MACT. Pursuant to section 112(d)(5), I
have decided not to issue MACT
standards and concluded that GACT is
appropriate for these four source
categories.
Legislative history describes GACT as
standards reflecting application of
generally available control technology,
that is, ‘‘methods, practices and
techniques which are commercially
available and appropriate for
application by the sources in the
category considering economic impacts
and the technical capabilities of the
firms to operate and maintain the
emissions control systems’’ (Senate
Report Number 101–228, December 20,
1989). In addition to technical
capabilities of the facilities and
availabilities of control measures,
legislative history suggests that we may
consider costs and economic impacts in
determining GACT, which is
particularly important when developing
regulations for source categories that
may have few establishments and many
small businesses, or when determining
whether additional control is necessary
for sources with emissions that are
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already well controlled as a result of
other existing or applicable standards.
Existing facilities in three of these
source categories are currently well
controlled as a result of State and
national standards and permitting
requirements for criteria pollutants that
obtain co-control of HAP. There are no
existing sources in the secondary copper
smelting source category. New and
existing area sources of polyvinyl
chloride (PVC) and copolymer plants
are subject to the National Emission
Standard for Vinyl Chloride (40 CFR
part 61, subpart F). The vinyl chloride
standard requires that new and existing
area sources also comply with the
National Emission Standard for
Equipment Leaks (Fugitive Emission
Sources) in 40 CFR part 61, subpart V.
New and existing area sources that
process beryllium ore, beryllium,
beryllium oxide, beryllium alloys, or
beryllium-containing waste are subject
to the National Emission Standard for
Beryllium (40 CFR part 61, subpart C).
One of the two primary zinc production
area sources is subject to the new source
performance standard (NSPS) at 40 CFR
part 60, subpart Q, and primary copper
smelting area sources are subject to the
NSPS at 40 CFR part 60, subpart P.
These NSPS, as well as other applicable
Federal and State requirements, are
incorporated into and enforced under
these primary zinc production and
primary copper smelting area sources’
title V permits.
Except for dioxin emissions from
secondary copper smelting, the urban
HAP emissions from the three area
source categories for nonferrous metals
are all metal HAP. Under the Federal
standards mentioned above that are
applicable to these three categories, we
are able to control the urban metal HAP
emissions by controlling emissions of
particulate matter (PM), which provide
co-control of the HAP metals for PM.
The Secondary Copper Smelting source
category does not have any existing
plants—plants that were operating in
1990 have permanently closed, and no
new plants have started. As discussed in
more detail in sections III through VI of
this preamble, we conclude that, with
the exception of secondary copper
smelting, GACT is equivalent to the
levels of control that are currently
required and being implemented by
sources in the other three categories.
Because there is not currently any, nor
is there expected to be any existing
source of secondary copper smelting, we
are not proposing a standard for existing
sources but are proposing a standard for
new area sources of secondary copper
smelting.
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III. Proposed NESHAP for Polyvinyl
Chloride and Copolymers Production
Area Sources
A. What area source category is affected
by the proposed NESHAP?
The Polyvinyl Chloride and
Copolymers Production area source
category includes facilities that
polymerize vinyl chloride monomer
alone or in combination with other
materials to produce PVC and
copolymers. Sources in this area source
category are currently subject to the
National Emission Standard for Vinyl
Chloride (40 CFR part 61, subpart F).
The vinyl chloride standard applies to
all new and existing major and area
sources of PVC and copolymer
production.
We estimate that there are
approximately 28 major sources of PVC
and copolymer production facilities
operating in the U.S. Although we do
not know of any existing area sources in
this category, we cannot say
conclusively that there are not and
never will be any area sources in this
category. Consequently, we are
proposing standards for both new and
existing area sources. We are requesting
comments on whether there are or ever
will be any area sources in this source
category.
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B. What HAP are emitted from polyvinyl
chloride and copolymers production?
The resins used to make PVC and
copolymer products are produced in
batch reactor processes where vinyl
chloride is polymerized with itself as a
homopolymer or copolymerized with
varying amounts of vinyl acetate,
ethylene, propylene, vinylidene
chloride, or acrylates. The resulting
resins are generally dried into nontoxic
powders or granules that are
compounded with auxiliary ingredients
and converted into a variety of plastic
end products. These end products can
be used in a large number of
applications, including latex paints,
coatings, adhesives, clear plastics, rigid
plastics, and flooring.
The urban HAP emitted from PVC and
copolymer production is vinyl chloride,
which is used as a primary feedstock.
The copolymer feedstocks (e.g., vinyl
acetate and vinylidene chloride) are also
HAP under CAA section 112(b) but are
not listed as urban HAP. HAP may be
released from an opening or leak in the
process equipment. Residual HAP (i.e.,
unreacted vinyl chloride) in the product
may also become airborne.
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C. What are the proposed requirements
for area sources?
1. Applicability and Compliance Dates
The proposed NESHAP apply to both
new and existing PVC and copolymer
plants that are area sources. Because
existing area sources, if there are any,
would already be operating subject to
emissions limits and work practice
standards that are the same as those in
this proposed NESHAP, we are
proposing that owners or operators of
existing sources comply with all the
requirements of the area source
NESHAP by [Date of publication of the
final rule in the Federal Register]. The
owner or operator of a new source
would be required to comply with the
area source NESHAP by [DATE OF
PUBLICATION OF THE FINAL RULE
IN THE Federal Register] or at startup,
whichever is later.
2. Emissions Limitations and Work
Practice Standards
We are proposing to adopt as the
NESHAP for the Polyvinyl Chloride and
Copolymer Production area source
category 40 CFR part 61, subpart F.
Subpart F establishes numerical
emissions limits for reactors; strippers;
mixing, weighing, and holding
containers; monomer recovery systems;
emissions sources following the
stripper(s); and reactors used as
strippers. Subpart F also establishes
both emissions limits and work practice
requirements that apply to discharges
from manual vent valves on a PVC
reactor and relief valves in vinyl
chloride service, fugitive emissions
sources, and equipment leaks. Subpart F
requires a new or existing source to
comply with the requirements at 40 CFR
part 61, subpart V for the control of
equipment leaks.
3. Compliance Requirements
We are proposing to include in this
proposed NESHAP the monitoring,
testing, recordkeeping, and reporting
requirements in 40 CFR part 61, subpart
F. The proposed NESHAP requires a
vinyl chloride continuous emissions
monitoring system (CEMS) for the
regulated emissions sources (except for
sources following the stripper) and for
any control system to which reactor
emissions or fugitive emissions must be
ducted. Plants using a stripper to
comply with the NESHAP must also
determine the daily average vinyl
chloride concentration for each type of
resin. The proposed NESHAP requires
the owner or operator to submit
quarterly reports containing information
on emissions or resin concentrations
that exceed the applicable limits.
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Records are required to demonstrate
compliance, including a daily operating
log for each reactor. Plants also would
be required to comply with the testing,
monitoring, recordkeeping, and
reporting requirements in the part 61
General Provisions (40 CFR part 61,
subpart A). We are also proposing that
the owner or operator comply with the
requirements for startup, shutdown, and
malfunction (SSM) plans and reports in
40 CFR 63.6(e)(3). We have explicitly
identified in the proposed NESHAP the
applicable General Provisions of both 40
CFR parts 61 and 63.
D. What is our rationale for selecting the
proposed standards for area sources?
1. Selection of Proposed Standards
Stripping is the primary control
measure used at major sources of PVC
and copolymer production facilities to
control HAP emissions and meet the
vinyl chloride emissions limits required
by 40 CFR part 61, subpart F, which
applies to both major and area sources
in this category. Stripping at the
production stage to recover unreacted
feedstock reduces the air emissions from
the product by reducing the residual
HAP in the product. In addition to
stripping, other HAP control measures
that may be employed to meet the
subpart F standards include: (1)
operating under a closed-vent system
with add-on control (e.g., flare) to
incinerate HAP gases not returning to
the process, and (2) minimizing the
presence of HAP before opening a
reactor or piece of process equipment
containing vinyl chloride monomer and
other HAP. Subpart F also requires
facilities to comply with the work
practice standards for ongoing leak
detection and repair prescribed in 40
CFR part 61, subpart V. As shown in
major source facilities, these
conventional control techniques and
work practices are readily available and
highly effective in controlling vinyl
chloride emissions at PVC and
copolymer production facilities.
Although we are not aware of any
existing area source, we have no reason
to believe that the conventional control
techniques employed at major sources
to meet the emissions limits and work
practice standards in subpart F are
infeasible, impractical, or inappropriate
for area sources. Therefore, we have
determined that the emissions control
requirements at 40 CFR part 61, subpart
F represent GACT for new and existing
sources in the Polyvinyl Chloride and
Copolymer Production area source
category.
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2. Selection of Proposed Compliance
Requirements
We have reviewed the compliance
requirements in the vinyl chloride
standard and part 61 General Provisions
applicable to this proposed NESHAP
and concluded that these requirements
are sufficient to ensure compliance with
the proposed emissions limits and work
practice standards. Therefore, we are
including the part 61, subpart F
performance test, monitoring
requirements, and recordkeeping
requirements in this proposed rule.
The General Provisions applicable to
the subpart F standard (40 CFR part 61,
subpart A), are necessary for effective
application of the subpart F standard
and are therefore incorporated into this
proposed rule as well. We are also
incorporating certain provisions in the
General Provisions of part 63, subpart A
to address aspects of this proposed rule
not covered by the part 61 General
Provisions. Specifically, we need to
incorporate certain provisions in §§ 63.1
and 63.5 of the part 63 General
Provisions which delineate
applicability, construction, and
reconstruction. However, we are not
applying provisions within 40 CFR 63.1
and 63.5 that are already covered by
part 61 General Provisions. We are
proposing to apply the provisions in 40
CFR 63.1(a) except for the provisions in
40 CFR 63.1(a)(11) and (12) regarding
notices, time periods, and postmarks; 40
CFR 63.1(b) except paragraph (b)(3); 40
CFR 63.1(c); 40 CFR 63.1(e); and 40 CFR
63.5 except for the references to 40 CFR
63.6 for compliance procedures and the
references to 40 CFR 63.9 for
notification procedures. Because the
part 61 General Provisions do not
include requirements for SSM plans and
reports, we are also proposing to require
the owner or operator of a new or
existing area source to comply with the
SSM requirements in 40 CFR 63.6(e)(3)
except for the requirement in 40 CFR
63.6(e)(3)(ix) to include the SSM
provisions in the title V permit.
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E. What is our rationale for exempting
polyvinyl chloride and copolymers
production area sources from the CAA
title V permit requirements?
Section 502(a) of the CAA provides
that EPA may exempt one or more area
sources from the requirements of title V
if EPA finds that compliance with such
requirements is ‘‘impracticable,
infeasible, or unnecessarily
burdensome’’ on such area sources. EPA
must determine whether to exempt an
area source from title V at the time we
issue the relevant section 112 standard
(40 CFR 70.3(b)(2)). We are proposing in
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this action to exempt PVC and
copolymers production area sources
from the requirements of title V. PVC
and copolymers production area sources
would not be required to obtain title V
permits solely as a function of being the
subject of the proposed NESHAP;
however, if they were otherwise
required to obtain title V permits, such
requirement(s) would not be affected by
the proposed exemption.
Consistent with the statute, EPA has
found that compliance with title V
permitting is ‘‘unnecessarily
burdensome’’ for PVC and copolymers
production area sources. EPA’s inquiry
into whether this criterion was satisfied
was based primarily upon consideration
of the following four factors: (1)
Whether title V would result in
significant improvements to the
compliance requirements that we are
proposing for this area source category;
(2) whether title V permitting would
impose a significant burden on these
area sources and whether that burden
would be aggravated by any difficulty
these sources may have in obtaining
assistance from permitting agencies; (3)
whether the costs of title V permitting
for these area sources would be
justified, taking into consideration any
potential gains in compliance likely to
occur for such sources; and (4) whether
there are implementation and
enforcement programs in place that are
sufficient to assure compliance with this
NESHAP without relying on title V
permits.
Additionally, EPA also considered,
consistent with the guidance provided
by the legislative history of CAA section
502(a),2 whether exempting PVC and
copolymers production area sources
would adversely affect public health,
welfare or the environment. We first
determined the extent to which these
factors were present for this area source
category. We then determined whether
those factors collectively demonstrated
that compliance with title V
requirements would be unnecessarily
burdensome for PVC and copolymer
production area sources.
The first factor is whether title V
would result in significant
improvements to the compliance
requirements we are proposing for this
area source category. We looked at the
compliance requirements of the
proposed NESHAP to see if they were
substantially equivalent to the
2 The legislative histroy of section 502(a) suggests
that EPA should not grant title V exemptions where
doing so would adversely affect public health,
welfare, or the environment. (See Chafee-Baucus
Statement of Senate Managers, Environment and
Natural Resources Policy Division 1990 CAA Leg.
Hist. 905, Compiled November, 1993.)
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monitoring, recordkeeping and
reporting requirements of title V (see 40
CFR 70.6 and 71.6) that we believe are
important for assuring compliance with
the NESHAP. The purpose of this
review was to determine if title V is
‘‘unnecessary’’ to improve compliance
with this NESHAP. A finding that title
V would not result in significant
improvements to the compliance
requirements in the proposed NESAHP
would support a conclusion that title V
permitting is ‘‘unnecessary’’ for area
sources in this category. One way that
title V may improve compliance is by
requiring monitoring (including
recordkeeping designed to serve as
monitoring) to assure compliance with
the emission limitations and control
technology requirements imposed in the
standard. The authority for adding new
monitoring in the permit is in the
‘‘periodic monitoring’’ provisions of 40
CFR 70.6(a)(3)(i)(B) and 40 CFR
71.6(a)(3)(i)(B), which allow new
monitoring to be added to the permit
when the underlying standard does not
already require ‘‘periodic testing or
instrumental or noninstrumental
monitoring (which may consist of
recordkeeping designed to serve as
monitoring).’’ In addition, title V
imposes a number of recordkeeping and
reporting requirements that may be
important for assuring compliance.
These include requirements for a
monitoring report at least every 6
months, prompt reports of deviations,
and an annual compliance certification.
See 40 CFR 70.6(a)(3) and 40 CFR
71.6(a)(3), 40 CFR 70.6(c)(1) and 40 CFR
71.6(c)(1), and 40 CFR 70.6(c)(5) and 40
CFR 71.6(c)(5).
To determine whether title V permits
would add significant compliance
requirements to the proposed NESHAP
for PVC and copolymer area sources, we
compared the title V monitoring,
recordkeeping, and reporting
requirements mentioned above to those
requirements in the proposed NESHAP
for the Polyvinyl Chloride and
Copolymer Production area source
category, which adopts the compliance
requirements in the National Emission
Standard for Vinyl Chloride. See 40 CFR
61.60. We also reviewed the part 61
compliance requirements (specifically
40 CFR 61.67 through 61.71) applicable
to this proposed NESHAP. The
proposed NESHAP would require a
vinyl chloride CEMS for the regulated
emissions sources (except for sources
following the stripper) and for any
control system to which reactor
emissions or fugitive emissions must be
ducted. Plants using a stripper to
comply with the NESHAP must also
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determine the daily average vinyl
chloride concentration for each type of
resin. Because both the continuous and
noncontinuous monitoring methods
required by the proposed NESHAP
would provide periodic monitoring, title
V would not add any monitoring to the
proposed NESHAP.
We also considered the extent to
which title V could enhance compliance
for area sources through recordkeeping
or reporting requirements, including
title V requirements for a 6-month
monitoring report, deviation reports,
and an annual compliance certification
in 40 CFR 70.6 and 71.6. The proposed
NESHAP requires the owner or operator
to submit quarterly reports containing
information on emissions or resin
concentrations that exceed the
applicable limits. Records are required
to demonstrate compliance, including a
daily operating log for each reactor, all
emissions measurements, and leak
detection and repair. The information
required in the proposed NESHAP is
similar to the information that must be
provided in the deviation reports and
semiannual monitoring reports required
under 40 CFR 70.6(a)(3) and 40 CFR
71.6(a)(3). The proposed NESHAP does
not require an annual compliance
certification report, which is a
requirement of a title V permit. See 40
CFR 70.5(c)(9)(iii) and 40 CFR
71.6(c)(5)(i). EPA believes that the
annual certification reporting
requirement is not a significant
compliance requirement because the
quarterly reports are adequate to ensure
compliance.
The monitoring, recordkeeping and
reporting requirements in the proposed
NESHAP for the Polyvinyl Chloride and
Copolymers Production area source
category are substantially equivalent to
such requirements under title V.
Therefore, we conclude that title V
would not result in significant
improvements to the compliance
requirements we are proposing for this
area source category.
The second factor we considered is
whether title V permitting would
impose significant burdens on these
area sources and whether that burden
would be aggravated by any difficulty
these sources may have in obtaining
assistance from permitting agencies. The
information collection request (ICR) for
parts 70 and 71 describes the title V
burdens and costs in the aggregate, and
although they do not focus on area
sources, they do describe the various
activities undertaken by title V sources,
including area sources, so many of the
same burdens and costs described in the
ICR will also apply to area sources.
Some examples of this burden include
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reading and understanding permit
program guidance and regulations,
completing the permit application,
preparing and submitting applications
for permit revisions every 5 years, and
paying permit fees. We believe that this
cost is a significant burden for these
area sources based on our general
assessment of this area source category.
The third factor we considered is
whether the costs of title V permitting
for these area sources would be
justified, taking into consideration any
potential gains in compliance likely to
occur for such sources. We found above
that the costs of title V would be a
significant burden on these area sources.
Also, based on our consideration of
factor 1 (described above) and factor 4
(described below), we did not identify
potential gain in compliance with this
proposed NESHAP from title V
permitting. Therefore, we conclude that
the costs of title V permitting for this
area source category are not justified.
The fourth factor we considered is
whether there are implementation and
enforcement programs in place that are
sufficient to assure compliance with this
NESHAP without relying on title V
permits. A conclusion that this criteria
can be met would support a conclusion
that Title V permitting is ‘‘unnecessary’’
for these area sources. See 70 FR 15254.
There are State programs in place to
enforce this area source NESHAP. We
believe that these programs are
sufficient to assure compliance with this
NESHAP. In addition, EPA retains
authority to enforce this NESHAP
anytime under CAA sections 112, 113
and 114. In light of the above, we
conclude that title V permitting is
‘‘unnecessary’’ to assure compliance
with this NESHAP because the statutory
requirements for implementation and
enforcement of this NESHAP by the
delegated States and EPA are sufficient
to assure compliance with this area
source NESHAP, in all parts of the U.S.,
without title V permits. In addition,
small business assistance programs
required by CAA section 507 may be
used to assist area sources that have
been exempted from title V permitting.
Also, States and EPA often conduct
voluntary compliance assistance,
outreach, and education programs
(compliance assistance programs),
which are not required by statute. These
additional programs supplement and
enhance the success of compliance with
this area source NESHAP. In light of all
of the above, we conclude that there are
implementation and enforcement
programs in place that are sufficient to
assure compliance with this NESHAP
without relying on title V permitting.
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In addition to evaluating whether
compliance with title V requirements is
‘‘unnecessarily burdensome’’, EPA also
considered, consistent with guidance
provided by the legislative history of
section 502(a), whether exempting PVC
and copolymer production area sources
from title V requirements would
adversely affect public health, welfare,
or the environment. One of the primary
purposes of the title V permitting
program is to clarify, in a single
document, the various and sometimes
complex regulations that apply to
sources in order to improve
understanding of these requirements
and to help sources to achieve
compliance with the requirements. In
this case, however, we do not believe
that a title V permit is necessary for us
to understand all requirements
applicable to PVC and copolymers
production area sources. To our
knowledge, currently the only
applicable requirements to these area
sources are 40 CFR part 61, subpart F.
This proposal would not add new
requirements to PVC and copolymers
production area sources. We have
determined that the subpart F
requirements reflect GACT and thus
adopted them in this proposed rule.
Furthermore, we do not find subpart F
standards to be very complicated to
understand or implement. For these
reasons, we do not find that title V
permitting is necessary to improve
understanding of and achieve
compliance with these standards.
Therefore, we conclude that exempting
these area sources from title V
permitting requirements in this
proposed rule would not adversely
affect public health, welfare, or the
environment.
Based on the above analysis, we
conclude that title V permitting would
be ‘‘unnecessarily burdensome’’ for PVC
and copolymer production area sources.
We are, therefore, proposing that this
area source category be exempt from
title V permitting requirements.
IV. Proposed NESHAP for Primary
Copper Smelting Area Sources
A. What area source category is affected
by the proposed NESHAP?
1. Source Category Description
Copper metal produced directly from
copper ore is referred to as ‘‘primary
copper.’’ The primary copper smelting
source category includes facilities that
produce copper from copper sulfide ore
concentrates using a pyrometallurgical
process.
Currently, there are three primary
copper smelters operating in the U.S.
Two of these smelters are major sources
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of HAP emissions and are subject to the
NESHAP for primary copper smelters in
40 CFR part 63, subpart QQQ. The third
smelter is an area source and is not
subject to the NESHAP in subpart QQQ,
which only applies to major sources.
Each of the three primary copper
smelters is located in relatively close
proximity to the copper mines
supplying the copper ore. Copper ore
excavated from mines is beneficiated to
produce copper ore concentrate. The ore
concentrates are first dried to reduce the
moisture content. The dried concentrate
then is blended with fluxes and
secondary copper-bearing materials.
This mixture is fed to a flash smelting
furnace where the ore is melted and
reacts to produce copper matte, a
molten solution of copper sulfide mixed
with iron sulfide.
The copper matte from the smelting
furnace is converted to blister copper
(approximately 98 percent pure copper)
by oxidization to remove the sulfur as
sulfur dioxide (SO2) gas and the iron as
a ferrous oxide slag. The molten slag
from converting is cooled and may be
processed in slag concentrators to
remove residual copper before on-site
disposal. The SO2 gases from smelting
and converting are vented to a sulfuric
acid plant. Copper converting is
conducted as a batch process in which
molten matte is charged to large
horizontal, cylindrical vessels or as a
continuous process in which solid matte
granules are fed to a flash smelting
furnace-like vessel.
Molten blister copper is transferred
from the converting vessel to an anode
furnace for refining to further remove
residual impurities and oxygen. The
blister copper is reduced in the anode
furnace to remove oxygen, typically by
injecting natural gas and steam to
produce a high purity copper. The
molten copper from the anode furnace
is poured into molds to produce solid
copper ingots called anodes. The anode
copper is sent to a copper refinery,
either on-site or at another location,
where it is further purified using an
electrolytic process to obtain the highpurity copper that is sold as a product.
The overall function of a primary
copper smelter, regardless of the
technologies used, is to produce anode
copper from copper ore concentrates.
However, there are key differences
between how the anode copper is
produced at a smelter using flash copper
converting technology compared to
smelters use batch copper converting
technology. These differences allow a
smelter using flash copper converting
technology to have inherently lower
potential HAP emissions than a smelter
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2. Existing Sources
The primary copper smelter that is an
area source uses flash copper converting
technology. At this smelter, molten
copper matte tapped from a flash
smelting furnace is not transferred as
molten material directly to the
converting vessel as is performed at the
two major source smelters that use batch
copper converting technology. Instead,
the matte is first quenched with water
to form solid granules of copper matte.
These matte granules are then ground to
a finer texture and fed to the flash
converting furnace. This furnace differs
significantly in design and operation
from the cylindrical batch converters
operated at the other U.S. smelters.
Also, only one flash converting furnace
is needed at the area source smelter
compared to multiple batch copper
converter vessels at the other smelters.
Most of the process fugitive emissions
associated with smelters using batch
copper converting do not occur in the
flash copper converting process. There
are no crane transfers of molten material
in open ladles between the smelting,
converting, and anode refining
departments. In addition, because flash
copper converting is conducted in an
enclosed vessel as a continuous process,
no process off-gases escape capture,
which occurs during the cyclic rollingout of the batch copper converters for
charging, skimming, and pouring.
While potential HAP emissions are
overall lower from flash copper
converting due to the elimination of
emissions points, the blister copper
produced by the continuous flash
copper converter may contain higher
levels of residual metal HAP impurities
than that produced by the batch copper
converting technology. At the smelter
using flash copper converting, however,
the anode furnaces and casting
operations are vented to emissions
control equipment that is effective in
controlling metal HAP emissions from
these processes that follow the flash
copper converting process.
southeastern Arizona. Production at two
of these mines is planned to start within
the next several years.
Increased copper mine development
in the U.S. does not automatically
trigger the building of new primary
copper smelters. For instance, there
have been no announcements that new
smelters are planned to be built or
would be necessary to process the
copper ore from the new mine
developments. The output from these
new mines will probably be processed
using the alternative hydrometallurgical
process because of economic and
technological advantages. This wet
process involves leaching, solvent
extraction, and electrowinning steps
instead of the high temperature smelting
and converting steps used for the
pyrometallurgical process.
The hydrometallurgical process is
conducted in facilities built near the
mine site. This process is preferable for
low copper content ores because of
lower production costs compared to the
costs of smelting and refining the ore.
Further, because it is a wet process and
does not use any operations involving
high temperatures and the handling of
molten materials, the potential for
emission of HAP metals to the
atmosphere is very low.
Hydrometallurgical processes are not
included in the Primary Copper
Smelting area source category.
Although smelters will not be used in
association with the new mining
projects mentioned above, we recognize
that the record-high commodity prices
for refined copper may encourage
construction of new primary copper
smelters in the U.S. Currently, copper
smelting technologies other than the
batch and flash copper converting
technologies are commercially available
and are being selected for new smelters
in other countries. Because these
smelting technologies are more
technologically advanced and cost
effective in producing copper than the
technologies currently employed at the
three existing U.S. smelters, they would
likely be used in the U.S. if new
smelters are constructed.
3. New Sources
Record-high commodity prices for
refined copper are motivating
companies to expand copper production
capacity in the U.S. and other countries
to meet higher demand. The
announcement of several new copper
mine projects in the southwestern U.S.
indicates that primary copper
production will be increasing in the
foreseeable future. For example, three
copper mine projects currently are
planned for development in
B. What HAP are emitted from primary
copper smelters?
Metals other than copper naturally
occur in copper ore deposits, and some
of these metals are listed as HAP under
CAA section 112(b). In general, the HAP
metals that have been found in larger
quantities in copper ore mined and
smelted in the U.S. are lead and arsenic.
Lesser quantities of antimony,
beryllium, cadmium, chromium, cobalt,
manganese, mercury, nickel, and
selenium have also been detected. As
using batch copper converting
technology.
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previously mentioned, the primary
copper smelting area source category
was listed for regulation under CAA
sections 112(c)(3) and 112(k)(3)(B) due
to emissions of the urban HAP arsenic,
cadmium, chromium, nickel, and lead.
HAP metals in the copper ore are
released into the atmosphere in the form
of PM during certain high temperature
operations. The composition and
quantity of the potential HAP emissions
from a given smelter are directly related
to the level of metal impurities in the
copper concentrate processed at the
smelter.
C. What are the proposed requirements
for area sources?
1. Applicability and Compliance Dates
The proposed NESHAP applies to
each new or existing primary copper
smelter that is an area source of HAP.
Because the one existing area source is
already operating subject to PM control
requirements that are the same as those
in this proposed NESHAP, we are
proposing that an existing affected
source comply by [DATE OF
PUBLICATION OF THE FINAL RULE
IN THE Federal Register]. A new
affected source would be required to
comply by [DATE OF PUBLICATION
OF THE FINAL RULE IN THE Federal
Register] or upon initial startup,
whichever is later.
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2. Emissions Limits and Work Practice
Standards
The owner or operator of an existing
area source would be required to control
HAP emissions from copper concentrate
drying, copper concentrate smelting,
copper matte drying and grinding,
copper matte converting, and copper
anode refining and casting operations.
The proposed NESHAP requires that
gases and fumes generated by these
processes be captured and vented
through one or more PM control
devices. Total PM emissions from the
captured gas streams from all of these
processes would be limited on a
smelter-wide basis to no greater than
89.5 pounds per hour (lb/hr) as
determined on a 24-hour average basis.
Similarly, the owner or operator of a
new area source would be required to
control HAP emissions from all primary
copper smelting processes, including
but not limited to those processes
mentioned above that are applicable to
the new sources’s smelter design. The
proposed standard requires that gases
and fumes generated by these processes
at a new source be captured and vented
through one or more PM control
devices. However, instead of the 89.5 lb/
hr emissions limit, we would require a
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new source to achieve a facility inputbased emission rate for total PM no
greater than a daily (24-hour) average of
0.6 pounds per ton (lb/ton) of copper
concentrate feed charged to the smelting
vessel.
The proposed NESHAP also require a
secondary gas system for each smelting
vessel and converting vessel that
collects the gases and fumes released
during the molten material transfer
operations and conveys the collected
gas stream to a control device. Capture
systems that collect gas and fumes and
convey them to a control device also
would be required for operations in the
anode refining and casting department.
3. Compliance Requirements
For existing area sources, we are
proposing to apply the testing,
monitoring, recordkeeping, and
reporting requirements for PM
emissions currently applicable to the
only existing area source smelter.
Compliance with the proposed
emissions limit for existing area sources
would be based on the daily average PM
emissions measured by a PM CEMS.
The owner or operator would submit
reports of deviations within two weeks
of the date the deviation occurred,
monthly summaries of monitoring data,
and semiannual monitoring reports. We
are also proposing that the owner or
operator comply with the requirements
in 40 CFR 63.6(e)(3) for SSM plans and
reports.
The owner or operator of an existing
area source would be required to
comply with notification requirements
in 40 CFR 63.9 of the General Provisions
(40 CFR part 63, subpart A). In the
notification of compliance status
required in 40 CFR 63.9(h), the owner
or operator would be allowed to certify
initial compliance with the proposed
emissions limit based on monitoring
data collected during the previous
month. The owner or operator would
also certify initial compliance with the
work practice standards.
The owner or operator of a new
primary copper smelter would be
required to install, operate, and
maintain a CEMS to measure and record
PM concentrations and gas stream flow
rates for each emissions source subject
to the emissions limit. The proposed
NESHAP requires that the PM CEMS
meet EPA Performance Specification 11
(40 CFR part 60, appendix B). A device
to measure and record the weight of the
copper concentrate feed charged to the
smelting furnace each day also would be
required. The owner or operator would
be required to continuously monitor PM
emissions, determine and record the
daily (24-hour) value for each day, and
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calculate and record the daily average
pounds of total PM per ton of copper
concentrate feed charged to the smelting
furnace. A monthly summary report of
the daily averages of PM per ton of
copper concentrate feed charged to the
smelting vessel also would be required.
All notification, monitoring, testing,
operation and maintenance,
recordkeeping, and reporting
requirements of the part 63 General
Provisions would apply to the owner or
operator of a new source.
D. What is our rationale for selecting the
proposed standards for area sources?
1. Selection of Pollutants
The HAP emissions from primary
copper smelters originate primarily from
metal impurities that naturally occur in
copper ore concentrates. During the
smelting process and the subsequent
converting process to produce blister
copper, these HAP metal species either
are eliminated in the molten slag tapped
from the process vessels or are
vaporized and discharged in the offgases vented from the vessels. HAP
metals may also be emitted from other
processes that contain molten materials,
such as anode refining and the casting
operation. Upon cooling of the process
off-gas, the volatilized HAP metal
species condense, form aerosols, and
behave as PM.
The composition and amounts of
metal HAP in the copper ore
concentrates can vary from one smelter
to another, as well as over time at
individual smelters depending on the
ore deposit from which the copper ore
concentrate is obtained. This inherent
variability and unpredictability of the
metal HAP compositions and amounts
in copper ore concentrates have a
material effect on the composition and
amount of HAP metals in the process
off-gas emissions at the smelter. As a
result, establishing individual
numerical emissions limits for each
HAP metal species is difficult given the
level of uncertainty about the individual
metal HAP compositions of the copper
ores processed at a smelter.
An emissions characteristic common
to all smelters and similar source
categories is that metal HAP are a
component of the PM contained in the
process off-gas discharged from
smelting, converting, anode refining,
and casting operations. Emissions limits
established to achieve control of PM
will also achieve control of metal HAP
other than mercury. Consequently, we
chose to use PM as a surrogate for the
urban HAP, which are metal HAP, in
establishing emissions limits. This
approach is consistent with the
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approach we used for the emissions
limits established in the NESHAP for
primary copper smelters in 40 CFR part
63, subpart QQQ.
2. Selection of Proposed Standards
We are aware of only one existing
primary copper smelter that is an area
source. This smelter was built in the
mid-1990’s and uses flash copper
converting technology. The smelter was
originally designed to use the most
advanced controls that were available at
that time to achieve emissions
reductions that met or exceeded levels
required to comply with the existing
State and Federal requirements to
control PM emissions. Extensive
emissions controls and work practices
are used for all process and fugitive PM
emissions sources at this smelter to
control PM and therefore metal HAP
emissions.
The existing area source smelter
operates emissions control systems that
capture and control off-gases from the
copper concentrate drying, smelting,
converting, and anode refining and
casting operations. All process gases
from these copper smelting operations
are routed to control devices (for many
sources, a series of control devices) that
achieve high-efficiency removal of PM
and metal HAP from the gas stream
before being discharged through a single
main stack. Also included in the
combined gas stream vented through
this main stack are captured gases and
fumes from the smelting and converting
furnaces’ tapping ports and launders
and from the matte drying and grinding
operations.
The work practices described above to
control PM and metal HAP emissions
are requirements in this area source
smelter’s current title V permit. The
smelter’s ability to demonstrate
compliance with these requirements on
a long-term basis indicates that the
facility owner has the technical and
economic capabilities to implement
these requirements, which are highly
effective in controlling PM and metal
HAP emissions. Therefore, we conclude
that these requirements reflect GACT for
primary copper area source smelters.
The source has a total PM emissions
limit for the main stack gases. This
facility-wide PM emissions limit for the
smelter process off-gases is based on the
operating practices and the emissions
control system configurations used at
this area source smelter. The maximum
allowable PM emissions level for the
smelter as measured at the main stack
is 89.5 lb/hr based on a 24-hour average.
A continuous sampling system that
measures PM is installed in the main
stack. Results from this continuous
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sampler are used to calculate the 24hour average for each day of the month
with a summary of the 24-hour averages
reported to the State each month for the
previous month.
PM and metal HAP emissions are
effectively controlled at this existing
area source by its compliance with the
facility-wide emissions limit and work
practice standards mentioned above,
which are requirements in its title V
permit. Although these requirements in
certain aspects are specific to this
facility, we think it is appropriate to
adopt these requirements as the
standards for existing sources of
primary copper production because this
is the only existing area source in this
source category.
We are not certain that a new smelter
would use flash copper converting
technology, and if it did, that it would
be in the configuration installed at the
existing smelter. A new smelter may use
one of the other commercially available
continuous smelting and converting
technologies that are based on bath
smelting technology or an innovative
new continuous copper smelting and
converting process that is not yet in
commercial operation.
Because a new primary copper
smelter may use a distinctly different
converting technology from the flash
copper converting technology, the
format of the emissions limit we are
proposing to adopt as an existing source
requirement is not appropriate for a new
source. For reasons set forth below, we
believe that an input-based emissions
limit is appropriate for new sources.
Emissions limits based on production
levels can be input-based (i.e., based on
raw materials consumed in making a
product) or output-based (i.e., based on
amount of product made). Because the
composition and quantity of the
potential metal HAP emissions from a
given smelter are directly related to the
level of metal impurities in the copper
concentrate, we decided that an inputbased emissions limit would be
appropriate for new sources. Using the
nominal design feed charge rate for the
smelting furnace, we calculated that the
89.5 lb/hr PM emissions limit for the
primary copper smelter would
correspond to an input-based PM
emissions limit of 0.6 lb/ton of copper
concentrate feed. We are proposing that
compliance with this emissions limit be
determined on a daily basis. Because
this input-based emissions limit is
derived from the 89.5 lb/hr daily
average emissions limit, it would ensure
that emissions from a new source are
limited at a level equivalent to the
emissions limit for the existing source.
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3. Selection of Proposed Compliance
Requirements
For existing area sources, we are
proposing to adopt the testing,
monitoring, recordkeeping, and
reporting requirements for PM
emissions currently applicable to the
only existing area source smelter. We
reviewed these requirements as
specified in the source’s title V permit
and concluded that these requirements
are sufficient to ensure compliance with
the proposed facility-wide emissions
limit and work practice standards.
These requirements include a PM
CEMS, reports of deviations, monthly
summaries of monitoring data, and
semiannual monitoring reports.
For new area sources, we would apply
the notification, testing, monitoring,
operation and maintenance,
recordkeeping, and reporting
requirements in the General Provisions
(40 CFR part 63, subpart A). The
General Provisions (40 CFR part 63,
subpart A) are necessary for effective
application of the standard for new area
sources and are therefore incorporated
into the proposed rule. These
requirements are sufficient to ensure
compliance with the proposed
emissions limit and work practice
standards.
Because permit information for the
existing facility does not identify
requirements for an SSM plan, we are
proposing that the owner or operator of
an existing or new area source be
required to comply with the SSM
requirements in 40 CFR 63.6(e)(3).
Section 63.6(e)(3)(ix) of the General
Provisions requires that the title V
permit for a source include provisions
for an SSM plan. According to Section
63.6(e)(3)(ix), the permit may fulfill this
requirement by citing the relevant
paragraphs of 40 CFR 63.6(e). Revisions
made to the plan do not constitute
permit revisions and the elements of the
plan are not applicable requirements
under 40 CFR 70.2 and 71.2.
V. Proposed NESHAP for Secondary
Copper Smelting Area Sources
A. What source category is affected by
the proposed NESHAP?
1. Source Category Description
A significant amount of copper metal
consumed in the U.S. has been
produced historically by remelting,
smelting, and refining scrap materials
containing copper. These scrap
materials can be recycled post-industrial
wastes, such as copper trimmings from
manufacturing processes or postconsumer wastes such as recovered old
consumer products containing copper.
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Copper metal produced from copper
scrap is referred to as ‘‘secondary
copper.’’
There is a variety of types of copper
scrap with varying copper contents.
High-quality unalloyed copper scrap
often contains more than 99 percent
copper and is remelted directly. Other
types of copper scrap have lower copper
contents and must be processed before
they can be reused in manufacturing
copper products. Types of copper scrap
with lower copper contents include
scrap from copper alloys (e.g., brass and
bronze scrap) and industrial residuals
that contain copper (e.g., skimmings,
ashes, refining slag, flue dusts). The
prices paid for copper scrap materials
depend on the commodity price for
refined copper and the type of scrap. In
general, prices for scrap copper track
refined copper price trends with higher
prices being paid for copper scrap
categories with higher copper purity.
Copper scrap referred to as old scrap
is obtained from used, worn out, or
obsolete copper products that are
recycled or recovered. This scrap is
obtained by collecting discarded,
dismantled or obsolete coppercontaining products at the end of their
service lives. Another source of old
scrap is copper building materials
salvaged from demolition sites.
Examples of old scrap include recycled
electrical cable and wiring, copper
plumbing pipes from building
demolitions, windings from worn
electric motors, salvaged automobile
radiators, dismantled printed circuit
boards, obsolete telephone switching
gear, recovered ammunition casings,
and copper-based spent catalysts. In
general, the copper content of old scrap
ranges from less than 30 to more than
98 percent copper depending on the
source. Old scrap typically requires
some pre-treatment, such as cleaning
and consolidation, in preparation for
smelting.
The other major category of copper
scrap, referred to as new scrap, is scrap
generated during manufacturing
processes and from other copper
materials that have never entered the
consumer markets. Examples of new
scrap include machining turnings,
stampings, and cuttings from
manufacturing processes, as well as
defective products pulled prior to
shipment. New scrap can often be
recycled directly with little or no
pretreatment. New scrap may be
collected and sold to third-party
secondary copper processors or may be
recycled directly within the
manufacturing facility that generates the
copper scrap.
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Facilities that process copper scrap
can be classified into three general
categories: smelters, ingot makers, and
remelters. The listing of this source
category included only secondary
copper smelters, which are the subject
of this proposed NESHAP. Secondary
copper smelters process copper scrap in
a blast furnace and converter or use
another pyrometallurgical purification
process to produce anode copper from
copper scrap, including low grade
copper scrap. The distinguishing
features of secondary copper smelters
are the type of pyrometallurgical
process used and the final product,
which is anode copper. Most U.S.
copper smelters charged low grade
copper scrap along with fluxes into a
cupola blast furnace followed by
additional purification in copper
converters. One facility processed lowgrade copper scrap using a combined
smelting and converting process
conducted in a top blown rotary
converter. All of these plants fire refined
the copper to produce anode copper.3
Secondary copper smelters may have
on-site pretreatment processes to clean
and consolidate the copper scrap in
preparation for smelting. Concentrating
can be performed either manually or
mechanically and can include sorting,
stripping, shredding, and magnetic
separation. The scrap can be further
refined using sweating, insulation
burning, drying, flotation, and leaching.
The type of pretreatment processes used
depends on the type and source of the
copper scrap.
A similarity with primary copper
producers is that the molten copper is
transferred from the converting vessel to
an anode furnace for additional fire
refining to further remove residual
impurities and oxygen. The molten
copper from the anode furnace is
poured into molds to produce solid
copper called anodes. The anode copper
is sent to a copper refinery, either onsite or at another location, where it is
further purified using an electrolytic
process to obtain the high-purity copper
that is used for manufacturing products.
Secondary copper smelters are part of
the broad standard industrial
classification (SIC) code 3341
(secondary nonferrous metals), which
also includes copper, brass, and bronze
ingot makers as well as producers of
several other secondary nonferrous
metals. The area source category listing
of secondary copper smelting, a small
subset of SIC 3341, was based on the
contribution of secondary copper
smelters to emissions of the urban HAP
3 There are no existing secondary copper smelters
as defined in the proposed rule.
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cadmium, lead and dioxin. For several
national emission standards, EPA has
defined source categories and
applicability based on the types of
processes in place rather than defining
applicability in terms of the broad
definition of an SIC code. In this case,
ingot makers and other producers of
certain secondary nonferrous metals
(other than secondary copper smelters
as defined in this proposed rule) are not
included in the secondary copper
smelting area source category.
2. Existing Sources
The secondary copper smelting plants
that served as the basis for emissions
estimates for the secondary copper
smelting area source category were
Gaston Recycling Industries (Gaston,
South Carolina), Franklin Smelting and
Refining (Philadelphia, Pennsylvania),
Cerro Copper Products (Sauget, Illinois),
Southwire Company (Carrollton,
Illinois), and Chemetco, Inc. (Hartford,
Illinois). All of these plants have shut
down, and no similar secondary copper
smelters have been constructed. There
are also no existing major source
secondary copper smelters.
Secondary copper smelting was once
a thriving industrial sector in the U.S.
with smelters operating in many regions
of the country. However, the last of the
smelters closed in the late 1990’s and
early 2000’s during a period of
depressed prices for refined copper,
increased production costs, and other
site-specific factors. In addition, scrap
copper collected in the U.S. was
increasingly exported to China and
other countries with little or no
processing, which increased the prices
U.S. secondary copper smelters paid for
scrap copper. The last U.S. secondary
copper smelter (Chemetco) closed in
2001. Our information indicates that
equipment and operations for secondary
copper production at these previously
operating smelters have all been
dismantled. Therefore, there is not any,
nor would there ever be, an existing
source secondary copper smelter that
would be subject to the proposed rule.
3. New Sources
While there are no existing secondary
copper smelters in the U.S., secondary
copper smelters are operating in several
other countries. Secondary copper
smelting technologies currently being
developed and utilized are significantly
different from the processes once used
at U.S. smelters. These new
technologies provide better control of
air emissions and produce inherently
lower HAP emission levels because they
do not have many of the fugitive
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emissions points associated with the
older smelting technologies.
Record-high commodity prices for
refined copper are motivating
companies to expand primary copper
production capacity in the U.S. If the
rebound in refined copper commodity
prices is stimulating the development of
primary copper production, it is
possible that these higher copper prices
will also encourage the return of the
secondary copper smelting industry to
the U.S. New secondary copper smelting
operations could be built by
independent companies to produce
refined copper for sale or by companies
that use copper as a raw material in
their manufacturing processes (e.g.,
electrical wire and cable
manufacturers).
The average price spread between
refined copper and copper scrap has
returned to the levels in the mid-1990’s
during which secondary copper
smelters operated profitably in the U.S.
The price spread levels that supported
the U.S. secondary copper smelting
industry in the past might have changed
in the late 1990’s because of new cost
considerations such as more stringent
pollution abatement requirements,
increased competition for the U.S. scrap
copper supply by foreign smelters, and
other factors. Based on the information
we have collected, however, we
conclude that the economic conditions
for secondary copper smelters are more
favorable today than they were in the
late 1990’s and early 2000’s when the
last U.S. smelters closed. Therefore, it is
possible that the industry will reemerge
in the U.S.
B. What HAP are emitted from
secondary copper smelters?
Copper scrap that is collected and
reprocessed may contain HAP metals,
including the urban HAP metals
cadmium and lead, for which secondary
copper smelters are listed for regulation
under CAA sections 112(c)(3) and
112(k)(3)(B). HAP metals occur in the
scrap as a result of other metals used in
conjunction with copper for certain
industrial and consumer applications,
such as the use of lead solders for
assembling copper plumbing pipes.
Metal HAP can be released into the
atmosphere in the form of PM during
certain high-temperature copper scrap
smelting operations.
As with metal HAP emissions from
primary copper smelters (see section
IV.B of this preamble), the presence and
concentrations of specific HAP metals
in a copper scrap material vary
depending on the material source.
Consequently, the potential HAP
emissions from a given secondary
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copper smelter are directly related to the
level of HAP metals in the copper scrap
material processed.
Secondary copper smelters were also
listed for emissions of the urban HAP
dioxin. Dioxins may form when
chlorinated plastics in the scrap are
heated to high temperatures in smelting
furnaces.
In EPA’s March 2005 Dioxin
Reassessment (available at https://
www.epa.gov/ncea/pdfs/dioxin/2kupdate/), secondary copper smelters
were identified as contributors to the
U.S. inventory of dioxin emissions in
1995 when three secondary copper
smelters were operating. Secondary
copper smelters have a high potential
for dioxin emissions because of the
abundance of chlorinated plastics in the
copper scrap that is used as feed
material.
C. What are the proposed requirements
for area sources?
1. Applicability and Compliance Dates
The proposed NESHAP apply to each
new secondary copper smelter that is an
area source of HAP. A new affected
source would be required to comply by
[DATE OF PUBLICATION OF THE
FINAL RULE IN THE Federal Register]
or upon initial startup, whichever is
later.
2. Emission Limit and Work Practice
Standards
We are proposing that any new
secondary copper smelter apply a
capture and control system for PM
emissions to any process operation that
melts copper scrap, alloys, or other
metals or that processes molten
material. Emissions of PM from the
control device must not exceed 0.002
grains per dry standard cubic feet (gr/
dscf). The owner or operator must also
prepare and follow a written plan for
the selection, inspection, and
pretreatment of copper scrap to
minimize, to the extent practicable, the
amount of oil and plastics in the scrap
that is charged to smelting or melting
furnaces.
3. Compliance Requirements
Fabric filters (baghouses) are expected
to be needed to meet the proposed
emission limit. Consequently, we are
proposing monitoring requirements that
include bag leak detection systems
when baghouses are used. The owner or
operator would keep records to
document conformance with
requirements in the written plan for the
selection, inspection, and pretreatment
of copper scrap. If a control device other
than a baghouse is used, the owner or
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operator would submit a monitoring
plan to the permitting authority for
approval. The monitoring plan would
include performance test results
showing compliance with the PM
emission limit, a plan for operation and
maintenance of the control device, a list
of operating parameters that will be
monitored, and operating parameter
limits that were established during the
performance test.
The owner or operator would conduct
a performance test to demonstrate initial
compliance with the PM emissions limit
and report the results in the notification
of compliance status required by 40 CFR
63.9(h) of the General Provisions. The
PM concentration would be determined
using EPA Method 5 (for negative
pressure baghouses) or Method 5D (for
positive pressure baghouses) in 40 CFR
part 60, appendix A. Repeat
performance tests would be required
every 5 years to demonstrate
compliance with the PM emissions
limit. All requirements of the part 63
General Provisions would apply to the
owner or operator of a new source.
D. What is our rationale for selecting the
proposed standards for area sources?
1. Selection of Proposed Standards
As discussed above, there is not and
will never be any existing area source
secondary copper smelter. Copper
production processes at all of the
previously existing secondary copper
smelters have been dismantled.
Construction or reconstruction would be
necessary should there be an attempt to
restart secondary copper production at
any of these facilities. Currently there is
not any such construction or
reconstruction at these facilities, and
construction or reconstruction that
occurs after this proposal would qualify
the operation as a new source. Because
there is not, nor will there ever be, any
existing area source secondary copper
smelter, a standard for existing area
sources of secondary copper smelters
would never have any application. We
do not believe that Congress intended
that we issue regulations that will not
have any application. Therefore, we are
not proposing standards for existing
area sources of secondary copper
smelters.
In the 1990 Amendments to the CAA,
Congress directed EPA to identify 30
HAP that present the greatest threat to
public health in the largest number of
urban areas (urban HAP). (See sections
112(c)(3) and 112(k)(3)(B) of the CAA.)
The 1990 Amendments also directed
EPA to list sufficient area source
categories to account for 90 percent or
more of the emissions of each urban
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HAP and to address the urban HAP
emissions from the listed sources
through regulation. Secondary copper
smelting area sources contributed to
emissions of the urban HAP dioxin,
cadmium and lead; therefore, their
urban HAP emissions are among those
that EPA is directed to address.
Pursuant to this statutory obligation, we
have studied this area source category
and have concluded that emissions of
dioxin, cadmium and lead from these
sources have been eliminated and
therefore adequately addressed by the
shutdown of these facilities.
However, we are proposing standards
for new sources to ensure that any
potential emissions of these urban HAP
from future secondary copper smelting
area sources will be appropriately
controlled. For new secondary copper
smelters, we reviewed technologies that
have been applied to similar scrap
melting processes in the U.S. For
example, almost all electric arc furnaces
at steel mills that melt and recycle iron
and steel scrap are controlled by
baghouses, several are subject to a PM
limit of 0.002 gr/dscf or less, and over
90 percent of the PM test data collected
for the entire industry show that PM
emissions are less than 0.002 gr/dscf. In
addition, baghouses were identified as
the most effective PM control device
used for emissions from cupolas (the
same type of furnace as that used at
secondary copper smelters) that melt
metal scrap at iron and steel foundries.
The NESHAP for iron and steel
foundries (40 CFR part 63, subpart
EEEEE) established a PM limit of 0.002
gr/dscf for new cupolas that melt metal
scrap. We chose to apply a PM limit of
0.002 gr/dscf as GACT to all melting
furnaces and other furnaces that process
molten metal at a new secondary copper
smelter. This limit has been
demonstrated as achievable by both new
and existing similar furnaces that
process metal scrap, and it represents
the level of performance provided by
the recommended technology for PM in
this application (i.e., a baghouse). The
GACT determination for new sources is
also consistent with the United Nations
Environment Programme’s guidelines
on performance standards for new
secondary copper smelters (available at
https://www.pops.int/documents/
batbep_advance/intersessional_work/
default.htm.) The guidelines
recommend high efficiency PM removal
systems (such as fabric filters or
baghouses) and state that such systems
should achieve a PM level of 5
milligrams per cubic meter (0.002 gr/
dscf) for new secondary copper
smelters. As discussed earlier, the last
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secondary copper smelter (as defined for
this source category) shut down several
years ago, and new secondary copper
facilities are not likely to use the older
technology that would subject them to
this proposed rule. However, we are
requesting comment on whether the
proposed standard for new sources is
accurate representation of GACT for
new sources.
The United Nations Environment
Programme has published guidelines on
best available techniques to reduce
dioxin emissions from metallurgical
processes, including secondary copper
smelting available at https://
www.pops.int/documents/
batbep_advance/intersessional_work/
default.htm. One of the pollution
prevention measures is pre-sorting of
feed materials (scrap) to reduce the
presence of oils, plastics, and chlorine.
Other pollution prevention methods
include thermal de-coating and deoiling, milling and grinding with
density or pneumatic separation, and
stripping cable insulation. Emission
control devices include fume collection
with high efficiency PM removal (such
as fabric filters). The stringent proposed
PM emissions limit (0.002 gr/dscf)
would ensure that high efficiency
control devices for PM would be used.
We selected the pollution prevention
measures and the PM emissions limit as
GACT for dioxin emissions from new
secondary copper smelters. The owner
or operator of any new smelter must
develop and implement a written plan
for the selection, inspection, and
pretreatment of copper scrap to
minimize, to the extent practicable, the
amount of oil and plastics in the scrap
that is charged to the smelting furnace.
This is accomplished by preparing and
following a scrap management plan,
training scrap inspectors, and keeping
records to show the plan is
implemented.
2. Selection of Proposed Compliance
Requirements
We are proposing to base the
compliance requirements on the testing,
monitoring, operation and maintenance,
recordkeeping, and reporting
requirements in the General Provisions
(40 CFR part 63, subpart A). The
General Provisions are necessary for
effective application of the standard for
new area sources and are therefore
incorporated into the proposed rule.
These requirements are sufficient to
ensure compliance with the proposed
emissions limit and work practice
standards.
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VI. Proposed NESHAP for Primary
Nonferrous Metals—Zinc, Cadmium,
and Beryllium Area Sources
A. What area source category is affected
by the proposed NESHAP?
The Primary Nonferrous Metals-Zinc,
Cadmium, and Beryllium source
category includes establishments
primarily engaged in smelting and
refining of three nonferrous metals—
zinc, cadmium, and beryllium. There
are only two primary zinc smelters that
are currently operating in the U.S., and
both are area sources. One of the
smelters is subject to the NSPS for
primary zinc smelters (40 CFR part 60,
subpart Q), which applies to SO2
emissions from roasters and PM
emissions from sintering machines.
Both facilities have title V operating
permits including requirements for the
control of PM and SO2.
There are no cadmium smelters in the
U.S., and we do not expect any to be
built in the future. Cadmium minerals
are not found alone in commercially
viable deposits. Instead, cadmium is
produced as a by-product of zinc
smelting processes. Only one of the two
U.S. primary zinc smelters produces
cadmium as a by-product; the other
plant shutdown and dismantled their
cadmium recovery process equipment.
All new and existing primary
beryllium production facilities are
subject to the National Emissions
Standard for Beryllium at 40 CFR part
61, subpart C. Recent data indicate that
there are no primary beryllium
production facilities (major or area
sources) currently operating in the U.S.
The last U.S. beryllium production
facility, which was a major source due
to emissions of tetrachloroethylene,
shutdown all primary beryllium
operations at its manufacturing plant in
June 2000. In the event that this plant
restarts the primary beryllium
production operation, the plant would
probably continue to be a major source
rather than an area source due to
tetrachloroethylene emissions.
B. What is primary zinc production and
what HAP are emitted?
Primary zinc smelters process zinc
sulfide ore concentrates to produce
metallic zinc or zinc oxide. Primary zinc
production facilities also process zinc
scrap and zinc oxide materials, and
although these may be considered
secondary zinc processes, they are part
of this area source category when they
are located at the primary zinc
production facility. The two U.S.
primary zinc producers process zinc
sulfide ore concentrate by smelting the
ore in a roaster to produce impure zinc
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oxide (calcine) followed by
hydrometallurgical reduction processes
that include leaching, purification, and
electrolysis to produce metallic zinc.
During roasting, most of the sulfur in
the ore concentrate is removed as SO2.
The roaster off-gases containing PM and
SO2 are processed through a series of
gas cleaning devices to remove the PM
(cyclones, electrostatic precipitators,
and venturi scrubbers), and the cleaned
gas is routed to a sulfuric acid plant
where the SO2 is converted to sulfuric
acid. Any HAP metals that volatilize
during the roasting process are removed
by the PM control equipment prior to
the acid plant. The PM removal
equipment is an important and inherent
part of the production process because
the PM must be removed before the gas
is processed in the acid plant (e.g., to
protect and maintain the catalyst in the
acid plant).
In the electrolytic deposition process,
the desulfurized calcine from the roaster
is first processed through a series of
leaching and purification operations to
dissolve the zinc oxide into an
electrolyte solution. The solution is
poured into cells where metallic zinc is
recovered in a batch operation by
passing current through the electrolyte
solution causing zinc to deposit on an
aluminum cathode.
During the acid leaching step,
cadmium is precipitated from the
solution by adding zinc dust. The
cadmium precipitate is filtered and
formed into a cake. The cake may be
sold as a recyclable product or further
purified and cadmium metal recovered
using an electrolytic process similar to
that used for zinc. Recovered cadmium
may be melted in a furnace and poured
into casting molds. Molten cadmium
can also be charged to a second
oxidizing furnace that converts
cadmium metal into cadmium oxide.
Although HAP metals are present in
the PM from the roaster’s exhaust, the
roaster is not a significant source of
HAP metal emissions because of the
extensive cleaning of the gas to remove
PM prior to the acid plant. Melting
furnaces also generate metal HAP
emissions and PM emissions because of
the high temperatures used to heat the
materials. These furnaces are used to
melt the pure zinc from electrolysis,
alloys, and zinc scrap and dust for
recycling. Both plants use baghouses to
control PM and HAP metal emissions
from the various melting furnaces. The
HAP metals that have been reported
from primary zinc production include
arsenic, cadmium, lead, manganese,
mercury, and nickel, all of which are
identified by EPA as urban HAP. As
previously mentioned, the primary
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nonferrous area source category was
listed for regulation under CAA sections
112(c)(3) and 112(k)(3)(B) due to
emissions of all of these HAP except for
mercury.
C. What are the proposed requirements
for primary zinc production area
sources?
1. Applicability and Compliance Dates
The proposed NESHAP applies to the
owner or operator of a new or existing
primary zinc production facility that is
an area source of HAP emissions.
Because the two existing sources are
already operating subject to PM control
requirements that are the same as those
in the proposed NESHAP, we are
proposing that an existing affected
source comply by [DATE OF
PUBLICATION OF THE FINAL RULE
IN THE Federal Register]. A new
affected source would be required to
comply by [DATE OF PUBLICATION
OF THE FINAL RULE IN THE Federal
Register] or upon initial startup,
whichever is later.
2. Emissions Limits and Work Practice
Standards
We are proposing a work practice
standard for roasters at new and existing
sources. The proposed NESHAP
requires the owner or operator to
exhaust roaster off-gases to PM removal
equipment and a sulfuric acid plant.
Bypassing the sulfuric acid plant during
charging of the roaster would be
prohibited.
Emissions limits are proposed for the
different types of melting furnaces at
primary zinc production facilities. For
existing sources, we are proposing PM
limits of 0.93 lb/hr for zinc cathode
melting furnaces; 0.1 lb/hr for furnaces
that melt zinc dust, chips, and offspecification zinc materials; and 0.228
lb/hr for the combined exhaust from
furnaces that melt zinc scrap and alloys.
For new sources, we are proposing a PM
limit of 0.005 gr/dscf for the furnaces
mentioned above. In addition, we are
proposing limits of 0.014 gr/dscf for
anode casting furnaces and 0.015 gr/dscf
for cadmium melting furnaces at new
and existing sources.
Emissions limits also are proposed for
any sintering machine at a new or
existing area source facility. If there is
a sintering machine, the proposed
NESHAP requires the owner or operator
to comply with the PM limit at 40 CFR
60.172 and the opacity limit at 40 CFR
60.174(a) of the NSPS for primary zinc
smelters (40 CFR part 60, subpart Q).
3. Proposed Compliance Requirements
We are proposing to adopt for existing
area sources certain monitoring,
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recordkeeping, and reporting
requirements already applicable to the
two existing facilities that relate to PM
emissions control. The owner or
operator of an existing area source
would monitor baghouse pressure drop,
perform routine baghouse maintenance,
and keep records to document
compliance. In addition, we are
proposing to require repeat performance
tests (at least once every 5 years) for
existing sources. The proposed NESHAP
also would require a continuous opacity
monitoring system (COMS) for any
sintering machine in accordance with
40 CFR 60.175.
The owner or operator of an existing
area source would be required to
comply with initial notification
requirements in 40 CFR 63.9 of the
General Provisions. In the notification of
compliance status required by 40 CFR
63.9(h), the owner or operator would be
allowed to certify initial compliance
with the proposed HAP emissions limits
based on the results of a PM
performance test for each of the
regulated emissions sources conducted
within the past 5 years. The owner or
operator would also certify initial
compliance with the work practice
standards.
If an existing source has not
conducted a performance test to
demonstrate compliance with the
emissions limits for a furnace, the
proposed NESHAP requires that the
facility conduct a test according to the
requirements at 40 CFR 63.7 using EPA
Method 5 (40 CFR part 60, appendix A)
to determine the PM concentration or an
alternative method previously approved
by the permitting authority. For a
sintering machine, the owner or
operator would conduct a performance
test according to the procedures in 40
CFR 60.176(b) using EPA Method 5 to
determine the PM concentration and
EPA Method 9 (40 CFR part 60,
appendix B) to determine the opacity of
emissions.
As required in the existing permits,
the owner or operator would be required
to submit a notification to the
permitting authority of any deviation
from the requirements of the NESHAP.
The notification must describe the
probable cause of the deviation and any
corrective actions or preventative
measures taken. Existing facilities
would also submit semiannual
monitoring reports which clearly
describe any deviations. Records of all
required monitoring data and support
information also would be required. The
owner or operator of an existing area
source would also be required to
comply with the requirements in 40
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CFR 63.6(e)(3) of the General Provisions
for SSM plans and reports.
The owner or operator of a new area
source would be required to install and
operate a bag leak detection system for
each baghouse used to comply with a
PM emissions limit. In addition, we are
proposing to require repeat PM
performance tests (once every 5 years)
for each furnace at a new source. The
owner or operator would also be
required to install, operate, and
maintain a COMS for each sintering
machine according to EPA Performance
Specification 1 (40 CFR part 60,
appendix B).
The owner or operator of a new
affected source would demonstrate
initial compliance with the applicable
emissions limits by conducting a
performance test according to the
requirements at 40 CFR 63.7 and using
EPA 5 or 5D (40 CFR part 60, appendix
A), as applicable, to determine the PM
concentration. An initial performance
test would also be required for a
sintering machine according to the
methods and procedures in 40 CFR
60.176(b). All of the testing, monitoring,
operation and maintenance,
recordkeeping, and reporting
requirements of the part 63 General
Provisions would apply to a new area
source.
D. What is our rationale for selecting the
proposed standards for primary zinc
production area sources?
sroberts on PROD1PC70 with PROPOSALS
1. Selection of PM as a Surrogate for
Metal HAP
Because the types and quantities of
metal HAP vary in zinc ore, it is not
practical to establish individual
standards for each specific metal HAP
listed as an urban HAP that could be
present in zinc ore. Instead, we decided
to establish standards using PM as a
surrogate for these urban HAP metal
emissions. Controlling PM emissions
will also control the metal HAP since
these compounds are contained within
the PM, i.e., they are in the particulate
form as opposed to the gaseous form.
The available air pollution controls for
the particulate HAP metals are the same
as those used for PM controls at primary
zinc production plants. These controls
capture particulate HAP metals nonpreferentially along with other PM, thus
making PM a reasonable surrogate for
these HAP metals. We have used this
approach in several other NESHAP in
which PM was determined to be a
surrogate for the HAP metals in the PM.
2. Selection of Proposed Standards
The release of metal HAP from
primary zinc production occurs from
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three types of emissions sources: the
roasting of the zinc sulfide ore; the use
of furnaces to melt zinc, materials
containing zinc (e.g., dust, scrap),
alloys, and cadmium; and the operation
of sintering machines. The high
temperatures inherent in the roasters,
melting furnaces, and sintering
machines are sufficient to temporarily
volatize metals that can then become
entrained in the exhaust gases from the
process. The other major processes
performed at primary zinc production
facilities include leaching, purification,
and electrowinning. These are wet
processes and are not considered to be
sources of metal HAP emissions.
Roasters. The proposed rule requires
that metal HAP generated by roasters
under high temperatures be removed
with PM in the off-gases. The off-gases
from roasters would be controlled by
removing PM and HAP metals in the
form of PM in a series of PM removal
devices, and then the SO2-rich off-gases
would be exhausted to a sulfuric acid
plant. These controls, including a
sulfuric acid plant, have been installed
at the two existing sources to comply
with the National Ambient Air Quality
Standards for SO2, as well as the NSPS
for primary zinc smelters (40 CFR part
60, subpart Q) for one source.
While the sulfuric acid plants were
originally installed to recover sulfuric
acid as a by-product and to control SO2
emissions, the inherent design and
operating requirements of these plants
also provide effective control of PM and
metal HAP contained in roaster offgases. The sulfuric acid production
process involves the catalytic
conversion of the SO2 contained in the
off-gases to produce liquid sulfuric acid.
To optimize the process performance
and prevent extensive damage to the
catalysts and other critical process
equipment, the first step of the process
requires that the roaster off-gases be precleaned and conditioned. These
operations involve first passing the gas
stream through multiple control devices
for the removal of PM and to reduce gas
stream temperature. By using multiple
PM control devices in series
(multicyclones, electrostatic
precipitators, and venturi scrubbers) to
treat roaster exhaust gases before
entering the sulfuric acid plant, very
high overall PM and metal HAP removal
efficiencies are achieved. Consequently,
there is little or no PM or metal HAP
emitted in the tail gas from the sulfuric
acid plant. The primary constituent of
the final tail gas from the acid plant is
sulfuric acid mist, which is not a HAP.
Both of the existing primary zinc
production facilities treat their roaster
off-gases using multiple control and
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59315
conditioning technologies to remove PM
and metal HAP prior to the roaster offgases entering the catalytic conversion
beds. Because neither facility’s permit
contains non-sulfuric acid PM limits
and because we have no PM emissions
test data, we determined that a work
practice standard was appropriate for
the control of roaster off-gases. The
work practice standard requires the
roaster’s off-gases be exhausted to PM
removal equipment and a sulfuric acid
plant, thus ensuring a consistently high
level of metal HAP control for the offgases. In light of the effective control of
PM and metal HAP at these two existing
facilities, we decided that the work
practice standard currently being
implemented at these facilities
represents GACT for existing and new
area sources of primary zinc production.
We are not proposing emissions limits
for HAP metals or PM in the tail gases
from the sulfuric acid plants because we
do not believe such limits are necessary.
The vast majority of PM exiting with the
tail gas is sulfuric acid mist, which is
not a HAP. Because rigorous treatment
of the roaster off-gases to remove PM
and metal HAP is a necessary operating
condition for the sulfuric acid plant,
requiring that cleaned gases be vented to
a sulfuric acid plant ensures that
emissions of HAP metals are either
nonexistent or limited to trace amounts.
Furnaces. Potential sources of metal
HAP emissions at primary zinc
production facilities include a variety of
high temperature furnaces operated for
the purpose of melting zinc; cadmium;
zinc scrap, dust, or chips; alloying
metals; and producing anodes used in
the electrowinning process. All of the
melting furnaces currently in operation
at the two existing primary zinc
production facilities control emissions
with baghouses, which are highly
effective in controlling PM and metal
HAP emissions. Baghouses are widely
used throughout the metallurgical
industry to control emissions from
primary and secondary metal processes.
Therefore, we conclude that GACT for
controlling metal HAP emissions from
the furnaces at primary zinc production
facilities is proper operation of a
baghouse. We believe that the emissions
limits for these furnaces that we are
proposing to adopt reflect the level of
emissions control that can be achieved
by well-operated and well-maintained
baghouses.
The two existing primary zinc
production facilities currently hold title
V operating permits issued by their
respective State permitting agencies;
both permits contain PM emissions
limits for all furnace operations. We
determined that the PM emissions limits
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applicable to these emissions sources
are consistent with the expected
performance of such operations
controlled by well-operated and
maintained baghouses. The PM
emissions limits vary somewhat among
furnace operations, which is indicative
of differences in processes associated
with the function of each furnace rather
than any real difference in performance
of the baghouse control devices.
Therefore, we decided that the PM
emissions limits in the operating
permits represent the performance
capabilities of baghouses at existing
affected sources. Because baghouse
technology is the best technology that
can be applied to these sources, the
permit limits that apply to the existing
furnaces controlled by baghouses also
represent the performance that can be
expected at new sources.
We are proposing a PM emissions
limit of 0.93 lb/hr for zinc cathode
melting furnaces at existing facilities.
This emissions limit is the permit limit
in effect for the zinc cathode melting
furnace at one of the primary zinc
production facilities. The other facility
has a permit limit for PM of 0.67 lb/hr.
We selected the 0.93 lb/hr limit because
it is achievable by zinc cathode melting
furnaces at both facilities, both facilities
use baghouses to reduce PM emissions,
and there is very little difference in the
magnitude of the PM emissions limits
for the two plants. The proposed PM
limit for zinc cathode melting furnaces
at existing facilities will ensure that the
baghouses will be operated and
maintained in a manner that will
continue to effectively reduce PM
emissions and metal HAP emissions.
We considered trying to develop an
emissions limit in a PM concentration
format, but decided against that
approach because concentration limits
were not available for both facilities,
and there was no basis on which to
derive a concentration-based limit that
would be appropriate for zinc cathode
melting furnaces at both plants. We also
considered a limit expressed as lb/ton
melted in the furnace. However, our
review and discussions with plant
personnel indicated that a short term
melting rate is difficult to determine and
can be subject to significant
inaccuracies. The plants do not weigh
the charge materials, and melting is a
batch process that involves charging the
furnace, melting, and tapping. Also, the
furnaces are operated intermittently. All
of these factors make it difficult to
determine an accurate melting rate in
tons per hour for the furnace during a
performance test run that typically lasts
for one hour.
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For new sources, it is not practical to
prescribe an emissions limit in lb/hr
because we do not know what the size
and configuration of the process will be.
One of the primary zinc facilities has a
concentration limit of 0.005 gr/dscf for
the zinc cathode melting furnace that is
applied in combination with their lb/hr
PM emissions limit. This concentration
limit has been met by baghouses in
many similar applications at existing
sources, such as electric arc furnaces at
steel plants (most are subject to a limit
of 0.0052 gr/dscf), iron and steel
foundries, and other metal processing
operations. We chose the limit of 0.005
gr/dscf as GACT for new zinc cathode
melting furnaces because it can be
achieved by properly designed and
operated baghouses.
One of the facilities has a baghouse
applied to treat the combined exhaust
from electric furnaces used to melt scrap
zinc and zinc alloys. This baghouse is
subject to a PM emissions limit of 0.228
lb/hr. The other facility operates a
smaller furnace for melting zinc dust,
zinc chips, and off-specification zinc
materials. This furnace is equipped with
a baghouse and is subject to a PM
emissions limit of 0.1 lb/hr. These
emissions limits will ensure that the
GACT technology (baghouses) or
equally effective control device will be
used, well-maintained, and welloperated to control PM and HAP metal
emissions from these furnaces at
existing sources. Therefore, we are
proposing to adopt these emissions
limits as the standards for existing
sources of primary zinc production.
As with a zinc cathode furnace at a
new source, it is similarly impractical to
prescribe PM emissions limits in lb/hr
for any of the other melting furnaces
because we do not know the size and
configuration of any new process, which
is necessary information for establishing
such a limit. Further, we have no test
data, nor do the title V permits for
existing sources contain limits in
concentration units that might be
applied to these types of melting
furnaces for new sources. However, like
zinc cathode melting furnaces, these
furnaces are used to melt materials
containing zinc. Thus, the concentration
of PM emissions is expected to be
similar to that from the zinc cathode
melting furnace. Consequently, we are
proposing to adopt the 0.005 gr/dscf
limit that is required for the zinc
cathode melting furnace at one existing
facility as the standard in the proposed
rule for furnaces melting zinc scrap,
alloys, dust, chips, or off-specification
zinc materials at new sources. This limit
has been demonstrated as achievable at
other similar melting processes, and in
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this case, it can be achieved by properly
designed and operated baghouses.
Only one primary zinc production
facility recovers cadmium and operates
a cadmium melting furnace. The other
facility has stopped cadmium
production and dismantled the
equipment. Emissions from the one
cadmium melting furnace are controlled
by a baghouse, which is subject to a PM
limit of 0.015 gr/dscf. Similarly, only
one facility operates an anode casting
furnace, and this furnace is controlled
by a baghouse and subject to a PM
emissions limit of 0.014 gr/dscf.
Because PM and metal HAP emissions
are effectively controlled at these
furnaces, we are proposing to include as
the standards for both new and existing
sources the PM limits of 0.015 gr/dscf
for cadmium melting furnaces and 0.014
gr/dscf for anode casting furnaces.
These limits are achievable by using
baghouses, the technology we have
identified as GACT for new and existing
sources, and will ensure effective
control for PM and HAP metals.
Sintering machine. Although neither
of the existing primary zinc production
facilities currently operates a sintering
machine, it is possible that one could be
installed at a new or existing facility.
The NSPS for primary zinc production
established a PM emission limit (0.022
gr/dscf) for new sintering machines. We
continue to believe that this PM
emissions limit will ensure that HAP
metals in the PM emissions from new
sintering machines will be well
controlled. We have no reason to believe
that this limit is infeasible, impractical
or inappropriate. Therefore, we chose
this emissions limit as GACT for
sintering machines at new and existing
area sources.
3. Selection of Proposed Compliance
Requirements
The title V permits of the two existing
area source smelters include general
recordkeeping and reporting
requirements for the facility and
detailed testing and monitoring
requirements for PM emissions from the
regulated emissions sources. We
reviewed these requirements and
concluded that they are sufficient to
ensure proper operation and
maintenance of baghouses and
compliance with the proposed work
practice standards for existing sources.
For example, both plants monitor
pressure drop to ensure baghouses are
operating properly, and there is little
benefit from retrofitting additional
monitoring technology to these existing
sources.
We are proposing to require bag leak
detection systems to monitor the
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sroberts on PROD1PC70 with PROPOSALS
performance of baghouses at new area
sources. These systems can be
incorporated into the design and
operation for new sources and would
not require retrofitting or duplicative
monitoring as would be the case if they
were applied to existing sources.
The part 63 General Provisions are
necessary for effective application of the
standard to existing sources and are
therefore incorporated into the proposed
rule. We would require that the plants
comply with the initial notification
requirements in 40 CFR 63.9. The initial
notification requirements would be
supplemented by other reporting
requirements that include notification of
any deviation and semiannual
monitoring reports, along with
recordkeeping requirements for
baghouse maintenance, monitoring data,
and other supporting information.
Section 63.6(e)(3)(ix) of the General
Provisions requires that the title V
permit for a source include provisions
for an SSM plan. Because permit
information for the existing facilities do
not identify requirements for an SSM
plan, the proposed NESHAP require the
owner or operator of an existing area
source to comply with the SSM
requirements in 40 CFR 63.6(e)(3).
According to 40 CFR 63.6(e)(3), the
permit may fulfill this requirement by
citing the relevant paragraphs of 40 CFR
63.6(e). Revisions made to the plan do
not constitute permit revisions and the
elements of the plan are not applicable
requirements under 40 CFR 70.2 and
71.2.
The part 63 General Provisions are
necessary for effective application of the
standard for new area sources and are,
therefore, incorporated into the
proposed rule. For new area sources, we
are proposing to apply the notification,
testing, monitoring, operation and
maintenance, recordkeeping, and
reporting requirements in the part 63
General Provisions. These requirements
are sufficient to ensure compliance with
the proposed emissions limit and work
practice standards.
E. What is primary beryllium production
and what HAP are emitted?
In the primary beryllium production
process, the ores bertrandite and beryl
are converted to a beryllium sulfate and
processed into beryllium hydroxide at
the mine site. A primary beryllium
production facility processes the
beryllium hydroxide to form metallic
beryllium, beryllium alloy, and/or
beryllium oxide.
Primary beryllium production
processes differ according to the end
product (i.e., metallic beryllium,
beryllium oxide, alloys). For metallic
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beryllium, the beryllium hydroxide is
first dissolved in an ammonia-fluoride
solution. The solution is neutralized,
heated to remove aluminum, and
filtered. The solution is then
crystallized; using centrifugation and
light washing, the crystals are
continuously removed and remaining
solution is sent to an evaporator. The
crystals (ammonium fluoroberyllate) are
charged into furnaces where they are
decomposed to beryllium fluoride and
ammonium fluoride. The ammonium
fluoride is recycled to the process, and
the molten beryllium fluoride is
removed from the furnace and
solidified; magnesium is added to
facilitate reduction. The mixture is
heated, causing beryllium to separate
and float on top of the slag. Both the
beryllium and slag are poured into a
graphite pot to solidify. Afterwards, the
product undergoes crushing and water
leaching in a ball mill. The resulting
beryllium pebbles contain 98 percent
beryllium along with slag and unreacted
magnesium. Impurities are removed by
melting the pebbles in induction
furnaces under vacuum. Excess
magnesium and beryllium fluoride from
the slag vaporize and are collected in
filters. Nonvolatiles, such as beryllium
oxide and magnesium fluoride, separate
from the metal as dross by adhering to
the bottom of the crucibles. The purified
metal is then poured and cast into
ingots.
To make beryllium oxide, the
beryllium hydroxide is dissolved in
water and sulfuric acid, resulting in a
beryllium sulfate solution. The solution
is filtered, evaporated, and crystallized.
The crystals are separated and the
beryllium sulfate is calcined in furnaces
to produce beryllium oxide. To make
beryllium-copper master alloys,
beryllium hydroxide, electrolytic
copper, and carbon are melted in an
electric arc furnace. The alloy is then
melted and cast into ingots. The master
alloy ingots are re-melted with
additional copper and other elements to
produce alloys with the desired metallic
characteristics.
The Toxics Release Inventory
indicates that the metal HAP emitted
from beryllium production processes
include primarily beryllium with lower
levels of the urban HAP nickel and lead.
HAP metals are emitted from the high
temperature furnaces that melt and
process beryllium compounds and those
that are used for producing beryllium
alloys. These furnaces include fluoride
decomposition furnaces that produce
beryllium fluoride from crystals of
ammonium fluoroberyllate, reduction
furnaces that process beryllium fluoride
to produce beryllium metal that is
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subsequently processed into pebbles,
vacuum induction furnaces used to
purify the beryllium pebbles, furnaces
that calcine beryllium sulfate to produce
beryllium oxide, and electric arc
furnaces used to produce beryllium
alloys such as beryllium-copper master
alloys. Baghouses (some in combination
with high efficiency particulate air
filters) and scrubbers are used to control
emissions of PM and HAP metals from
these furnaces.
F. What are the proposed requirements
for primary beryllium production area
sources?
1. Applicability and Compliance Dates
We are proposing to adopt as GACT
for beryllium production area sources
all of the requirements in the National
Emission Standard for Beryllium at 40
CFR part 61, subpart C. Because any
existing area source would have already
been operating in accordance with the
part 61 standard, we are proposing that
the owner or operator of an existing
source comply with the area source
NESHAP by [DATE OF PUBLICATION
OF THE FINAL RULE IN THE Federal
Register]. The owner or operator of a
new area source would be required to
comply by [DATE OF PUBLICATION
OF THE FINAL RULE IN THE Federal
Register] or at startup, whichever is
later.
2. Emissions Limits
We are proposing to adopt the part 61,
subpart C standard as the area source
NESHAP for both new and existing
primary beryllium production facilities.
The part 61, subpart C standard limits
emissions from extraction plants (i.e.,
primary beryllium production facilities)
to 10 grams (0.022 lb) of beryllium over
a 24-hour period. Alternatively, the
owner or operator of a beryllium
production facility may request to meet
an ambient concentration limit instead
of the emissions limit.
3. Compliance Requirements
We are proposing to include in the
proposed NESHAP the testing,
monitoring, recordkeeping, and
reporting requirements in 40 CFR part
61, subpart C. The owner or operator
would be required to conduct a
performance test using EPA Method 103
or 104 (40 CFR part 61, appendix B) to
demonstrate initial compliance with the
emissions limit. The proposed NESHAP
would not allow any changes, which
could potentially increase emissions
above the level determined in the most
recent performance test until a new
emissions test has been estimated by
calculation and reported to EPA. An
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owner or operator subject to the ambient
concentration limit must operate air
sampling sites to continuously monitor
the concentrations of beryllium in the
ambient air according to an EPAapproved plan. The owner or operator
must comply with recordkeeping
requirements in the proposed NESHAP
and the testing, monitoring,
recordkeeping, and reporting
requirements in the part 61 General
Provisions in 40 CFR part 61, subpart A.
We are also proposing that the owner or
operator comply with certain
requirements in the part 63 General
Provisions in 40 CFR part 63, subpart A,
including the requirements for SSM
plans and reports in 40 CFR 63.6(e)(3).
We have explicitly identified in the
proposed NESHAP the applicable
General Provisions of both 40 CFR parts
61 and 63.
G. What is our rationale for selecting the
proposed standards for primary
beryllium area sources?
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1. Selection of Pollutants
The major metal HAP reported by the
only primary beryllium plant when it
was operating its primary beryllium
process was beryllium. Nickel and lead,
which are urban HAP, were the only
other metal HAP reported (at much
smaller quantities than beryllium). Each
of these metal HAP are components of
PM, and the PM emission controls
installed for beryllium control other
metal HAP in the PM. Consequently, we
chose to use beryllium as a surrogate for
all of the HAP metal in the PM. The
emissions limits for beryllium and the
PM controls installed to meet the limits
will ensure that all HAP metals in the
PM from primary beryllium processes
are well controlled.
2. Selection of Proposed Standards
Currently no primary beryllium
production facilities operate in the U.S.
In recent years, there has been only one
U.S. producer, and this facility
shutdown all primary beryllium
operations in June 2000. This plant was
a major source due to emissions of
tetrachloroethylene. In the event this
plant restarted the primary beryllium
production operation, the plant would
probably continue to be a major source
rather than an area source due to
emissions of tetrachloroethylene.
Although all area source primary
beryllium production facilities that
previously existed have ceased to
operate, we do not have information
that would suggest that beryllium
production cannot be restarted at these
facilities. Therefore, we see a need to
establish standards for existing sources
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in the proposed rule to regulate any
previously existing source that may
restart its beryllium production.
Similarly, we do not have any
information that would suggest that
there are unlikely to be any new area
source production facilities. Therefore,
we also need to establish standards for
new sources.
We are proposing to adopt the part 61,
subpart C standard as the NESHAP for
the primary beryllium production area
source category. The part 61, subpart C
standard, which applies to new and
existing major and area sources, is a
stringent and effective air emissions
regulation. As a result of the part 61,
subpart C standard, the last primary
beryllium production facility in the U.S.
was highly effective in controlling
beryllium, PM, and metal HAP
emissions. As shown in this facility, to
meet the part 61, subpart C standard,
beryllium processing operations were
controlled using multiple air cleaning
systems that were also highly effective
in controlling emissions of PM and HAP
metals. For example, beryllium oxide
furnaces were controlled by baghouses,
packed tower scrubbers and demisters;
alloy induction furnaces were
controlled by baghouses and cartridge
filters; reduction furnaces were
controlled by wet cyclones and venturi
scrubbers; and vacuum casting was
controlled by cyclones, baghouses, and
cartridge filters. The highly effective
control of beryllium, PM, and metal
HAP emissions at this last facility
indicates that the part 61, subpart C
emissions limits are effective as well as
feasible. Although that facility was a
major source, we have no reason to
believe that such control is not
appropriate for an area source. The fact
that the part 61, subpart C standard
already applies to both major and area
sources suggest that they are appropriate
for area sources as well. Therefore, we
have determined that the emissions
limits in the part 61, subpart C standard
represents GACT for new and existing
beryllium production area sources.
3. Selection of Proposed Compliance
Requirements
We have reviewed the performance
test and monitoring requirements in the
part 61, subpart C standard and
reconfirmed their adequacy and
propriety for ensuring compliance with
the proposed emission limits. Therefore,
we are including the part 61, subpart C
performance test and monitoring
requirements in the proposed rule.
The General Provisions applicable to
the subpart C standard (40 CFR part 61,
subpart A), are necessary for effective
application of the subpart C standard
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and are therefore incorporated into the
proposed rule as well. We are also
incorporating certain provisions in the
General Provisions of part 63, subpart A
to address aspects of the proposed rule
not covered by the part 61 General
Provisions. Specifically, we need to
incorporate certain provisions in 40 CFR
63.1 and 63.5 that delineate
applicability, construction, and
reconstruction. However, we are not
applying provisions within 40 CFR 63.1
and 63.5 that are already covered by
part 61 General Provisions. We are
proposing to apply the provisions in 40
CFR 63.1(a) except for the provisions in
40 CFR 63.1(a)(11) and (12) regarding
notices, time periods, and postmarks; 40
CFR 63.1(b) except paragraph (b)(3); 40
CFR 63.1(c); 40 CFR 63.1(e); and 40 CFR
63.5 except for the references to 40 CFR
63.6 for compliance procedures and the
references to 40 CFR 63.9 for
notification procedures.
Because the part 61 General
Provisions do not include requirements
for SSM plans and reports, we are also
proposing to require the owner or
operator of a new or existing area source
to comply with the requirements in 40
CFR 63.6(e)(3). According to 40 CFR
63.6(e)(3), the permit may fulfill this
requirement by citing the relevant
paragraphs of 40 CFR 63.6(e). Revisions
made to the plan do not constitute
permit revisions and the elements of the
plan are not applicable requirements
under 40 CFR 70.2 and 71.2.
VII. Statutory and Executive Order
Reviews
A. Executive Order 12866: Regulatory
Planning and Review
Under Executive Order 12866 (58 FR
51735, October 4, 1993), this action is a
‘‘significant regulatory action’’ because
it may raise novel legal or policy issues.
Accordingly, EPA submitted this action
to OMB for review under Executive
Order 12866, and any changes made in
response to OMB recommendations
have been documented in the docket for
this action.
B. Paperwork Reduction Act
The proposed NESHAP for Polyvinyl
and Copolymers Production Area
Sources do not impose any new
information collection burden. New and
existing plants that are area sources
would be required to comply with the
same testing, monitoring, reporting, and
recordkeeping requirements as those in
the National Emission Standards for
Vinyl Chloride (40 CFR part 61, subpart
F), to which these area sources are
currently subject, and the information
collection requirements in the part 61
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NESHAP General Provisions (40 CFR
part 61, subpart A), which are
incorporated into the proposed
NESHAP. The OMB has previously
approved the information collection
requirements in 40 CFR part 61, subpart
F, under the provisions of the
Paperwork Reduction Act, 44 U.S.C.
3501 et seq. and has assigned OMB
control number 2060–0071, EPA
Information Collection Request (ICR)
number 0186.10.
A copy of the OMB-approved ICR for
the National Emission Standards for
Vinyl Chloride and Beryllium may be
obtained from Susan Auby, Collection
Strategies Division, U.S. EPA (2822T),
1200 Pennsylvania Ave., NW.,
Washington, DC 20460, by e-mail at
auby.susan@epa.gov, or by calling (202)
566–1672.
Burden means the total time, effort, or
financial resources expended by persons
to generate, maintain, retain, disclose, or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; develop, acquire,
install, and utilize technology and
systems for the purposes of collecting,
validating, and verifying information,
processing and maintaining
information, and disclosing and
providing information; adjust the
existing ways to comply with any
previously applicable instructions and
requirements; train personnel to be able
to respond to a collection of
information; search data sources;
complete and review the collection of
information; and transmit or otherwise
disclose the information.
An agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid OMB
control number. The OMB control
numbers for EPA’s regulations in 40
CFR part 63 are listed in 40 CFR part 9.
The proposed requirements for
primary beryllium production facilities
in the proposed NESHAP for Primary
Nonferrous Metals Area Sources do not
impose any new information collection
burden. New and existing plants that are
area sources would be required to
comply with the same testing,
monitoring, recordkeeping, and
reporting requirements as those in the
National Emission Standards for
Beryllium (40 CFR part 61, subpart C),
to which these area sources are
currently subject, and the information
collection requirements in the part 61
General Provisions (40 CFR part 61,
subpart A), which are incorporated into
the proposed NESHAP for these sources.
The OMB has previously approved
these information collection
requirements in 40 CFR part 61, subpart
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C, under the provisions of the
Paperwork Reduction Act, 44 U.S.C.
3501 et seq. and has assigned OMB
control number 2060–0092, EPA ICR
number 0193.08.
A copy of the OMB-approved ICR for
the National Emission Standards for
Vinyl Chloride and Beryllium may be
obtained from Susan Auby, Collection
Strategies Division, U.S. EPA (2822T),
1200 Pennsylvania Ave., NW.,
Washington, DC 20460, by e-mail at
auby.susan@epa.gov, or by calling (202)
566–1672.
Burden means the total time, effort, or
financial resources expended by persons
to generate, maintain, retain, disclose, or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; develop, acquire,
install, and utilize technology and
systems for the purposes of collecting,
validating, and verifying information,
processing and maintaining
information, and disclosing and
providing information; adjust the
existing ways to comply with any
previously applicable instructions and
requirements; train personnel to be able
to respond to a collection of
information; search data sources;
complete and review the collection of
information; and transmit or otherwise
disclose the information.
An agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid OMB
control number. The OMB control
numbers for EPA’s regulations in 40
CFR part 63 are listed in 40 CFR part 9.
The information requirements in the
proposed NESHAP for Polyvinyl
Chloride and Copolymers Production
Area Sources, Primary Copper Smelting
Area Sources, Secondary Copper
Smelting Area Sources, and Primary
Nonferrous Metals-Zinc, Cadmium, and
Beryllium Area Sources have been
submitted for approval to OMB under
the Paperwork Reduction Act, 44 U.S.C.
3501 et seq. The ICR document prepared
by EPA has been assigned EPA ICR
number 2240.01.
The proposed information collection
requirements are based on the current
title V permitting requirements for
existing sources and the information
collection requirements in the part 63
General Provisions (40 CFR part 63,
subpart A), most of which are
incorporated into the proposed
NESHAP for new sources. The ICR
document includes the burden estimates
for all applicable General Provisions.
These recordkeeping and reporting
requirements are mandatory pursuant to
section 114 of the CAA (42 U.S.C. 7414).
All information submitted to EPA
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59319
pursuant to the information collection
requirements for which a claim of
confidentiality is made is safeguarded
according to CAA section 114(c) and the
Agency’s implementing regulations at
40 CFR part 2, subpart B.
The PM testing, monitoring,
recordkeeping, and reporting
requirements with which existing
primary copper smelting and primary
zinc smelting area sources would be
required to comply under the proposed
NESHAP are the same as the
requirements that are in these facilities’
current title V operating permits. The
only new information collection
requirements that would apply to these
area sources would consist of initial
notifications and SSM plan, reporting,
and recordkeeping requirements. Any
new primary zinc production facility,
primary copper smelter, or secondary
copper smelter area source would be
subject to all information collection
requirements in the part 63 General
Provisions.
The annual burden for this
information collection averaged over the
first 3 years of this ICR is estimated to
total 9 labor hours per year at a cost of
$771 for the one existing primary
copper smelting area source and 18.5
labor hours per year at a cost of $1,566
for the two existing primary zinc
smelting area sources. No capital/
startup costs or operation and
maintenance costs are associated with
the proposed requirements. No costs or
burden hours are estimated for new
primary copper smelters, secondary
copper smelters, or primary zinc
production area sources because no new
sources are estimated during the 3-year
period of the ICR. No new sources have
been constructed in more than 10 years,
no new construction has been
announced, and we have no indication
there will be any new sources in the
next 3 years.
Burden means the total time, effort, or
financial resources expended by persons
to generate, maintain, retain, disclose, or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; develop, acquire,
install, and utilize technology and
systems for the purposes of collecting,
validating, and verifying information,
processing and maintaining
information, and disclosing and
providing information; adjust the
existing ways to comply with any
previously applicable instructions and
requirements; train personnel to be able
to respond to a collection of
information; search data sources;
complete and review the collection of
information; and transmit or otherwise
disclose the information.
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An agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid OMB
control number. The OMB control
numbers for EPA’s regulations in 40
CFR part 63 are listed in 40 CFR part 9.
To comment on the Agency’s need for
this information, the accuracy of the
provided burden estimates, and any
suggested methods for minimizing
respondent burden, including the use of
automated collection techniques, EPA
has established a public docket for this
action, which includes this ICR, under
Docket ID number EPA-HQ-OAR–2006–
0510. Submit any comments related to
the ICR for the proposed rules to EPA
and OMB. See ADDRESSES section at the
beginning of this notice for where to
submit comments to EPA. Send
comments to OMB at the Office of
Information and Regulatory Affairs,
Office of Management and Budget, 725
17th Street NW., Washington, DC 20503,
Attention: Desk Officer for EPA. Since
OMB is required to make a decision
concerning the ICR between 30 and 60
days after October 6, 2006, a comment
to OMB is best assured of having its full
effect if OMB receives it by November
6, 2006. The final rule will respond to
any OMB or public comments on the
information collection requirements
contained in this proposal.
C. Regulatory Flexibility Act
The Regulatory Flexibility Act (RFA)
generally requires an agency to prepare
a regulatory flexibility analysis of any
rule subject to notice and comment
rulemaking requirements under the
Administrative Procedure Act or any
other statute unless the agency certifies
that the rule would not have a
significant economic impact on a
substantial number of small entities.
Small entities include small businesses,
small not-for-profit enterprises, and
small governmental jurisdictions.
For the purposes of assessing the
impacts of the proposed area source
NESHAP on small entities, small entity
is defined as: (1) A small business that
meets the Small Business
Administration size standards for small
businesses found at 13 CFR 121.201
(less than 1,000 employees for primary
copper smelting and less than 750
employees for PVC and copolymers
production, secondary copper smelting,
and primary nonferrous metals
manufacturing); (2) a small
governmental jurisdiction that is a
government of a city, county, town,
school district, or special district with a
population of less than 50,000; and (3)
a small organization that is any not-forprofit enterprise which is independently
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owned and operated and is not
dominant in its field.
After considering the economic
impacts of the proposed rules on small
entities, I certify that this action will not
have a significant economic impact on
a substantial number of small entities.
There would not be adverse impacts on
existing area sources of PVC and
copolymer production facilities,
primary copper smelters, and nonferrous metal production facilities
because the proposed rules do not create
any new requirements or burdens other
than minimal notification requirements
for existing sources. There would be no
adverse impacts on existing secondary
copper area sources because there are no
existing sources in the category.
Although the proposed NESHAP
contain emission control requirements
for new area sources in all four source
categories, we are not aware of any new
sources being constructed now or
planned in the near future, and
consequently, we did not estimate any
impacts for new sources.
We continue to be interested in the
potential impacts of the proposed action
on small entities and welcome
comments on issues related to such
impacts.
D. Unfunded Mandates Reform Act
Title II of the Unfunded Mandates
Reform Act of 1995 (UMRA), Public
Law 104–4, establishes requirements for
Federal agencies to assess the effects of
their regulatory actions on State, local,
and tribal governments and the private
sector. Under section 202 of the UMRA,
EPA generally must prepare a written
statement, including a cost-benefit
analysis, for proposed and final rules
with ‘‘Federal mandates’’ that may
result in expenditures by State, local,
and tribal governments, in the aggregate,
or to the private sector, of $100 million
or more in any 1 year. Before
promulgating an EPA rule for which a
written statement is needed, section 205
of the UMRA generally requires EPA to
identify and consider a reasonable
number of regulatory alternatives and
adopt the least costly, most costeffective, or least burdensome
alternative that achieves the objectives
of the rule. The provisions of section
205 do not apply when they are
inconsistent with applicable law.
Moreover, section 205 allows EPA to
adopt an alternative other than the least
costly, most cost-effective, or least
burdensome alternative if the
Administrator publishes with the final
rule an explanation why that alternative
was not adopted. Before EPA establishes
any regulatory requirements that may
significantly or uniquely affect small
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governments, including tribal
governments, it must have developed
under section 203 of the UMRA a small
government agency plan. The plan must
provide for notifying potentially
affected small governments, enabling
officials of affected small governments
to have meaningful and timely input in
the development of EPA regulatory
proposals with significant Federal
intergovernmental mandates, and
informing, educating, and advising
small governments on compliance with
the regulatory requirements.
EPA has determined that the
proposed rules do not contain a Federal
mandate that may result in expenditures
of $100 million or more for State, local,
and tribal governments, in the aggregate,
or the private sector in any one year. As
discussed earlier in this preamble, the
estimated expenditures for the private
sector in any 1 year are less than $2,500.
Thus, the proposed rules are not subject
to the requirements of sections 202 and
205 of the UMRA. In addition, the
proposed rules do not significantly or
uniquely affect small governments. The
proposed rules contain no requirements
that apply to such governments, impose
no obligations upon them, and would
not result in expenditures by them of
$100 million or more in any one year or
any disproportionate impacts on them.
Therefore, the proposed rules are not
subject to section 203 of the UMRA.
E. Executive Order 13132: Federalism
Executive Order 13132 (64 FR 43255,
August 10, 1999) requires EPA to
develop an accountable process to
ensure ‘‘meaningful and timely input by
State and local officials in the
development of regulatory policies that
have federalism implications.’’ ‘‘Policies
that have federalism implications’’ are
defined in the Executive Order to
include regulations that have
‘‘substantial direct effects on the States,
on the relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government.’’
The proposed rules do not have
federalism implications. They would
not have substantial direct effects on the
States, on the relationship between the
national government and the States, or
on the distribution of power and
responsibilities among the various
levels of government, as specified in
Executive Order 13132. The proposed
rules impose requirements on owners
and operators of specified area sources
and not State and local governments.
Thus, Executive Order 13132 does not
apply to the proposed rules.
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F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
Executive Order 13175 (65 FR 67249,
November 6, 2000), requires EPA to
develop an accountable process to
ensure ‘‘meaningful and timely input by
tribal officials in the development of
regulatory policies that have tribal
implications.’’ The proposed rules do
not have tribal implications, as specified
in Executive Order 13175. They would
not have substantial direct effects on
tribal governments, on the relationship
between the Federal government and
Indian tribes, or on the distribution of
power and responsibilities between the
Federal government and Indian tribes,
as specified in Executive Order 13175.
The proposed rules impose
requirements on owners and operators
of specified area sources and not tribal
governments. Thus, Executive Order
13175 does not apply to the proposed
rules.
G. Executive Order 13045: Protection of
Children From Environmental Health
and Safety Risks
Executive Order 13045 (62 FR 19885,
April 23, 1997) applies to any rule that:
(1) is determined to be ‘‘economically
significant,’’ as defined under Executive
Order 12866, and (2) concerns an
environmental health or safety risk that
EPA has reason to believe may have a
disproportionate effect on children. If
the regulatory action meets both criteria,
EPA must evaluate the environmental
health or safety effects of the planned
rule on children, and explain why the
planned regulation is preferable to other
potentially effective and reasonably
feasible alternatives considered by EPA.
EPA interprets Executive Order 13045
as applying only to those regulatory
actions that are based on health or safety
risks, such that the analysis required
under section 5–501 of the Executive
Order has the potential to influence the
regulation. The proposed rules are not
subject to the Executive Order. They are
based on control technology and not on
health or safety risks.
sroberts on PROD1PC70 with PROPOSALS
H. Executive Order 13211: Actions That
Significantly Affect Energy Supply,
Distribution, or Use
The proposed rules are not a
‘‘significant energy action’’ as defined in
Executive Order 13211 (66 FR 28355,
May 22, 2001) because they are not
likely to have a significant adverse effect
on the supply, distribution, or use of
energy. Further, we have concluded that
these proposed rules are not likely to
have any adverse energy effects because
energy requirements would remain at
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existing levels. No additional pollution
controls or other equipment that would
consume energy are required by the
proposed rules.
I. National Technology Transfer
Advancement Act
Section 12(d) of the National
Technology Transfer and Advancement
Act (NTTAA) of 1995 (Pub. L. No. 104–
113, section 12(d), 15 U.S.C. 272 note)
directs EPA to use voluntary consensus
standards (VCS) in its regulatory
activities, unless to do so would be
inconsistent with applicable law or
otherwise impractical. The VCS are
technical standards (e.g., materials
specifications, test methods, sampling
procedures, and business practices) that
are developed or adopted by VCS
bodies. The NTTAA directs EPA to
provide Congress, through OMB,
explanations when the Agency does not
use available and applicable VCS.
The proposed rules involve technical
standards. The EPA cites the following
standards: EPA Methods 1, 1A, 2, 2A,
2C, 2D, 2F, 2G, 3, 3A, 3B, 4, 5, 5D, and
9 in 40 CFR part 60, appendix A; and
Performance Specification (PS) 1 and 11
in 40 CFR part 60, appendix B.
Consistent with the NTTAA, EPA
conducted searches to identify
voluntary consensus standards in
addition to these EPA methods. No
applicable VCS were identified for EPA
Methods 1A, 2A, 2D, 2F, 2G, 5D or 9.
The search and review results are in the
docket for this rule.
The search identified one VCS as an
acceptable alternative to EPA Method
3B. The method ASME PTC 19.10–1981,
‘‘Flue and Exhaust Gas Analyses,’’
(incorporated by reference-see 40 CFR
63.14) is cited in this rule for its manual
method for measuring the oxygen,
carbon dioxide, and carbon monoxide
content of the exhaust gas. This part of
ASME PTC 19.10–1981 is an acceptable
alternative to EPA Method 3B.
The standard ASTM D6216 (1998),
‘‘Standard Practice for Opacity Monitor
Manufacturers to Certify Conformance
with Design and Performance
Specifications,’’ was designated an
acceptable alternative for the design
specifications given in EPA’s PS–1
(promulgated in March 1983). As a
result, EPA incorporated ASTM D6216–
98 by reference into PS–1 as the design
specifications for opacity monitors in
August 2000.
The search for emissions
measurement procedures identified 13
other VCS. The EPA determined that
these 13 standards identified for
measuring emissions of the HAP or
surrogates subject to emission standards
in this proposed rule were impractical
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59321
alternatives to EPA test methods.
Therefore, EPA does not intend to adopt
these standards for this purpose. The
reasons for the determinations for the 13
methods are in the docket for this
proposed rule.
For the methods required or
referenced by the proposed rules, a
source may apply to EPA for permission
to use alternative test methods or
alternative monitoring requirements in
place of any required testing methods,
performance specifications, or
procedures under § 63.7(f) and § 63.8(f)
of subpart A of the General Provisions.
List of Subjects in 40 CFR Part 63
Environmental protection, Air
pollution control, Hazardous
substances, Reporting and
recordkeeping requirements.
Dated: September 27, 2006.
Stephen L. Johnson,
Administrator.
For the reasons stated in the
preamble, title 40, chapter I, part 63 of
the Code of Federal Regulations is
proposed to be amended as follows:
PART 63—[AMENDED]
1. The authority citation for part 63
continues to read as follows:
Authority: 42 U.S.C. 7401 et seq.
Subpart A—[AMENDED]
2. Section 63.14 is amended by
revising paragraph (i)(1) to read as
follows:
§ 63.14
Incorporations by reference.
*
*
*
*
*
(i) * * *
(1) ANSI/ASME PTC 19.10–1981,
‘‘Flue and Exhaust Gas Analyses [Part
10, Instruments and Apparatus],’’ IBR
approved for §§ 63.309(k)(1)(iii),
63.865(b), 63.3166(a)(3),
63.3360(e)(1)(iii), 63.3545(a)(3),
63.3555(a)(3), 63.4166(a)(3),
63.4362(a)(3), 63.4766(a)(3),
63.4965(a)(3), 63.5160(d)(1)(iii),
63.9307(c)(2), 63.9323(a)(3),
63.11155(e)(3), 11162(f)(3)(iii) and (f)(4),
11163(g)(1)(iii) and (g)(2), and Table 5 of
subpart DDDDD of this part.
*
*
*
*
*
3. Part 63 is amended by adding
subpart DDDDDD to read as follows:
Subpart DDDDDD—National Emission
Standards for Hazardous Air Pollutants
for Polyvinyl Chloride and Copolymers
Production Area Sources
Sec.
Applicability and Compliance Dates
63.11140 Am I subject to this subpart?
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63.11141
Federal Register / Vol. 71, No. 194 / Friday, October 6, 2006 / Proposed Rules
What are my compliance dates?
Standards and Compliance Requirements
63.11142 What are the standards and
compliance requirements for new and
existing sources?
Other Requirements and Information
63.11143 What General Provisions apply to
this subpart?
63.11144 What definitions apply to this
subpart?
63.11145 Who implements and enforces
this subpart?
Applicability and Compliance Dates
§ 63.11140
Am I subject to this subpart?
(a) You are subject to this subpart if
you own or operate a plant specified in
40 CFR 61.61(c) that produces polyvinyl
chloride (PVC) or copolymers and is an
area source of hazardous air pollutant
(HAP) emissions. Your plant is an area
source if it does not emit and does not
have the potential to emit either 10 tons
per year (tpy) or more of any single HAP
or 25 tpy or more of any combination of
HAP.
(b) This subpart applies to each new
or existing affected source. The affected
source is the collection of all equipment
and activities in vinyl chloride service
necessary to produce PVC and
copolymers. An affected source does not
include portions of your PVC and
copolymers production operations that
meet the criteria in 40 CFR 61.60(b) or
(c).
(1) An affected source is existing if
you commenced construction or
reconstruction of the affected source
before October 6, 2006.
(2) An affected source is new if you
commenced construction or
reconstruction of the affected source on
or after October 6, 2006.
(c) This subpart does not apply to
research and development facilities, as
defined in section 112(c)(7) of the Clean
Air Act (CAA).
(d) You are exempt from the
obligation to obtain a permit under 40
CFR part 70 or 40 CFR part 71, provided
you are not otherwise required by law
to obtain a permit under 40 CFR 70.3(a)
or 40 CFR 71.3(a). Notwithstanding the
previous sentence, you must continue to
comply with the provisions of this
subpart.
sroberts on PROD1PC70 with PROPOSALS
§ 63.11141
dates?
What are my compliance
(a) If you own or operate an existing
affected source, you must achieve
compliance with the applicable
provisions in this subpart by [DATE OF
PUBLICATION OF FINAL RULE IN
THE Federal Register].
(b) If you own or operate a new
affected source, you must achieve
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compliance with the applicable
provisions in this subpart by the dates
in paragraphs (b)(1) and (2) of this
section.
(1) If you startup a new affected
source on or before [DATE OF
PUBLICATION OF FINAL RULE IN
THE Federal Register], you must
achieve compliance with the applicable
provisions in this subpart not later than
[DATE OF PUBLICATION OF FINAL
RULE IN THE Federal Register].
(2) If you startup a new affected
source after [DATE OF PUBLICATION
OF FINAL RULE IN THE Federal
Register], you must achieve compliance
with the provisions in this subpart upon
startup of your affected source.
Standards and Compliance
Requirements
§ 63.11142 What are the standards and
compliance requirements for new and
existing sources?
You must meet all the requirements in
40 CFR part 61, subpart F, except for 40
CFR 61.62 and 40 CFR 61.63.
Other Requirements and Information
§ 63.11143 What General Provisions apply
to this subpart?
(a) All the provisions in 40 CFR part
61, subpart A, apply to this subpart.
(b) The provisions in 40 CFR part 63,
subpart A, applicable to this subpart are
specified in paragraphs (b)(1) through
(4) of this section.
(1) Section 63.1(a)(1) through (10).
(2) Section 63.1(b) except paragraph
(b)(3), § 63.1(c), and (e).
(3) Section 63.5 (preconstruction
review and notification requirements)
except for the references to § 63.6
(compliance with standards and
maintenance requirements) procedures
and the references to § 63.9 (notification
requirements).
(4) Section 63.6(e)(3) except for
§ 63.6(e)(3)(ix).
§ 63.11144
subpart?
What definitions apply to this
The terms used in this subpart are
defined in the CAA; 40 CFR 61.02; 40
CFR 61.61; and § 63.2 for terms used in
the applicable provisions of part 63,
subpart A, as specified in § 63.11143(b).
§ 63.11145 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 a State,
local, or tribal agency. If the U.S. EPA
Administrator has delegated authority to
a State, local, or tribal agency, then that
Agency has the authority to implement
and enforce this subpart. You should
contact your U.S. EPA Regional Office
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to find out if this subpart is delegated
to a State, local, or tribal agency within
your State.
(b) In delegating implementation and
enforcement authority of this subpart to
a State, local, or tribal agency under 40
CFR part 63, subpart E, the approval
authorities contained in paragraphs
(b)(1) through (4) of this section are
retained by the Administrator of the
U.S. EPA and are not transferred to the
State, local, or tribal agency.
(1) Approval of an alternative means
of emission limitation under 40 CFR
61.12(d).
(2) Approval of a major change to test
methods under 40 CFR 61.13(h). A
‘‘major change to test method’’ is
defined in § 63.90.
(3) Approval of a major change to
monitoring under 40 CFR 61.14(g). A
‘‘major change to monitoring’’ is defined
in § 63.90.
(4) Approval of a major change to
recordkeeping/reporting under 40 CFR
61.10. A ‘‘major change to
recordkeeping/reporting’’ is defined in
§ 63.90.
4. Part 63 is amended by adding
subpart EEEEEE to read as follows:
Subpart EEEEEE—National Emission
Standards for Hazardous Air Pollutants
for Primary Copper Smelting Area
Sources
Sec.
Applicability and Compliance Dates
63.11146 Am I subject to this subpart?
63.11147 What are my compliance dates?
Standards and Compliance Requirements
63.11148 What are the standards and
compliance requirements for existing
sources?
63.11149 What are the standards and
compliance requirements for new
sources?
Other Requirements and Information
63.11150 What General Provisions apply to
this subpart?
63.11151 What definitions apply to this
subpart?
63.11152 Who implements and enforces
this subpart?
Tables to Subpart EEEEEE of Part 63
Table 1 to Subpart EEEEEE of Part 63—
Applicability of General Provisions to
Subpart EEEEEE
Applicability and Compliance Dates
§ 63.11146
Am I subject to this subpart?
(a) You are subject to this subpart if
you own or operate a primary copper
smelter that is an area source of
hazardous air pollutant (HAP)
emissions. Your primary copper smelter
is an area source if it does not emit and
does not have the potential to emit
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either 10 tons per year (tpy) or more of
any single HAP or 25 tpy or more of any
combination of HAP.
(b) This subpart applies to each new
or existing affected source. The affected
source is each primary copper smelter.
(1) An affected source is existing if
you commenced construction or
reconstruction of the affected source
before October 6, 2006.
(2) An affected source is new if you
commenced construction or
reconstruction of the affected source on
or after October 6, 2006.
(c) This subpart does not apply to
research and development facilities, as
defined in section 112(c)(7) of the Clean
Air Act (CAA).
(d) If you own or operate an area
source subject to this subpart, you must
obtain a permit under 40 CFR part 70 or
40 CFR part 71.
§ 63.11147
dates?
What are my compliance
(a) If you own or operate an existing
affected source, you must achieve
compliance with the applicable
provisions of this subpart by [DATE OF
PUBLICATION OF FINAL RULE IN
THE Federal Register].
(b) If you own or operate a new
affected source, you must achieve
compliance with the applicable
provisions of this subpart by the dates
in paragraphs (b)(1) and (2) of this
section.
(1) If you startup a new affected
source on or before [DATE OF
PUBLICATION OF FINAL RULE IN
THE Federal Register], you must
achieve compliance with the applicable
provisions of this subpart not later than
[DATE OF PUBLICATION OF FINAL
RULE IN THE Federal Register].
(2) If you startup a new affected
source after [DATE OF PUBLICATION
OF FINAL RULE IN THE Federal
Register], you must achieve compliance
with the applicable provisions of this
subpart upon startup of your affected
source.
Standards and Compliance
Requirements
sroberts on PROD1PC70 with PROPOSALS
§ 63.11148 What are the standards and
compliance requirements for existing
sources?
(a) You must not discharge to the
atmosphere through any combination of
stacks or other vents captured process
exhaust gases from the copper
concentrate dryers, smelting vessels,
converting vessels, matte drying and
grinding plants, secondary gas systems,
and anode refining and casting
department that contain total particulate
matter (PM) in excess of 89.5 pounds
per hour (24-hour average).
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(b) For each smelting vessel and
converting vessel at your primary
copper smelter, you must operate a
secondary gas system that collects the
gases and fumes released during the
molten material transfer operations and
conveys the collected gas stream to a
control device.
(c) For operations in the anode
refining and casting department at your
primary copper smelter, you must meet
the requirements in paragraphs (c)(1)
and (2) of this section.
(1) For each vessel used to refine
blister copper, remelt anode copper or
anode scrap, or hold molten anode
copper, you must collect the gases and
fumes vented from the vessel and
convey the collected gas stream to a
control device.
(2) For each anode casting wheel, you
must collect gases and fumes vented
when casting molten anode copper and
convey the collected gas stream to a
control device.
(d) You must operate a continuous
emissions monitoring system (CEMS) to
measure and record PM concentrations
and gas stream flow rates for the exhaust
gases discharged to the atmosphere from
each emissions source subject to the
emissions limit in paragraph (a) of this
section. A single PM CEMS may be used
for the combined exhaust gas streams at
a point before the gases are discharged
to the atmosphere. Measured results
must be expressed as pounds of PM
emitted per hour calculated at the end
of each calendar day for the preceding
24-hour period. Collected PM CEMS
data must be made available for
inspection on a daily basis.
(e) You must demonstrate initial
compliance with the PM emissions limit
in paragraph (a) of this section based on
the results of a 24-hour average from the
PM CEMS. You may certify initial
compliance with the PM emissions limit
based on the results of sampling
conducted during the previous month.
(f) You must submit to the permitting
authority by the 20th day of each month
a summary of the 24-hour averages for
the previous month.
(g) You must submit written
notification to the permitting authority
of any deviation from the requirements
of this subpart, including those
attributable to upset conditions, the
probable cause of such deviations, and
any corrective actions or preventative
measures taken. You must submit this
notification within 14 days of the date
the deviation occurred.
(h) You must submit semiannual
monitoring reports to your permitting
authority. All instances of deviations
from the requirements of this subpart
must be clearly identified in the reports.
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59323
(i) You must retain records of all
required monitoring data and support
information. Support information
includes all calibration and
maintenance records, all original strip
charts or appropriate recordings for
continuous monitoring instrumentation,
and copies of all reports required by this
subpart. For all monitoring
requirements, the owner or operator
must record the following information,
where applicable:
(1) The date, place, and time of
sampling or measurement, the date
analyses were performed, the company
or entity that performed the analyses,
the analytical techniques or methods
used, the results of such analyses, and
the operating conditions existing at the
time of sampling or measurement.
(2) Records of activities performed to
assure proper operation and
maintenance of air emissions control
systems and monitoring systems or
devices.
§ 63.11149 What are the standards and
compliance requirements for new sources?
(a) You must not discharge to the
atmosphere through any combination of
stacks or other vents process exhaust
gases from the copper concentrate
dryers, smelting vessels, converting
vessels, matte drying and grinding
plants, secondary gas systems, and
anode refining and casting department
that contain total PM in excess of 0.6
pound per ton of copper concentrate
feed charged to the smelting vessel (24hour average).
(b) For each smelting vessel and
converting vessel at your primary
copper smelter, you must operate a
secondary gas system that collects the
gases and fumes released during molten
material transfer operations and convey
the collected gas stream to a control
device.
(c) For operations in the anode
refining and casting department at your
primary copper smelter, you must meet
the requirements in paragraphs (c)(1)
and (2) of this section.
(1) For each vessel used to refine
blister copper, remelt anode copper or
anode scrap, or hold molten anode
copper, you must collect the gases and
fumes vented from the vessel and
convey the collected gas stream to a
control device.
(2) For each anode casting wheel, you
must collect gases and fumes vented
when casting molten anode copper and
convey the collected gas stream to a
control device.
(d) You must install, operate, and
maintain a PM CEMS to measure and
record PM concentrations and gas
stream flow rates for the exhaust gases
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discharged to the atmosphere from each
emissions source subject to the
emissions limit in paragraph (a) of this
section. You must also install, operate,
and maintain a weight measurement
system to measure and record the
weight of the copper concentrate feed
charged to the smelting furnace on a
daily basis. A single PM CEMS may be
used for the combined exhaust gas
streams at a point before the gases are
discharged to the atmosphere. For each
PM CEMS used to comply with this
paragraph, you must meet the
requirements specified in paragraphs
(d)(1) through (3) of this section.
(1) You must install, certify, operate,
and maintain the PM CEMS according
to the applicable specification and
testing requirements of EPA
Performance Specification 11 in 40 CFR
part 60, appendix B, and the quality
assurance requirements of Procedure 2
in 40 CFR part 60, appendix F.
(2) You must conduct an initial
performance evaluation of the PM
CEMS according to the requirements of
Performance Specification 11 in 40 CFR
part 60, appendix B. Thereafter, you
must perform the performance
evaluations as required by Procedure 2
in 40 CFR part 60, appendix F.
(3) You must perform quarterly
accuracy determinations and daily
calibration drift tests for the PM CEMS
according to Procedure 2 in 40 CFR part
60, appendix F.
(e) To demonstrate compliance with
the PM emissions limit in paragraph (a)
of this section, you must continuously
monitor and record PM emissions,
determine and record the daily (24hour) value for each day, and calculate
and record the daily average pounds of
total PM per ton of copper concentrate
feed charged to the smelting furnace.
The daily average must be calculated at
the end of each calendar day for the
preceding 24-hour period. You must
maintain records of the calculations of
daily averages with supporting
information and data, including
measurements of the weight of copper
concentrate feed charged to the smelting
vessel. Collected PM CEMS data must
be made available for inspection on a
daily basis.
(f) You must demonstrate initial
compliance with the emissions limit in
paragraph (a) of this section using the
procedures in paragraph (e) of this
section. You must complete this initial
compliance demonstration within 180
days after startup and report the results
in your notification of compliance status
no later than 30 days after the end of the
compliance demonstration.
(g) You must submit to the permitting
authority by the 20th day of each month
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a summary of the daily average PM per
ton of copper concentrate feed charged
to the smelting vessel for the previous
month.
Other Requirements and Information
63.11150 What General Provisions apply
to this subpart?
(a) If you own or operate an existing
or new affected source, you must
comply with the requirements of the
General Provisions (40 CFR part 63,
subpart A) as specified in Table 1 to this
subpart and paragraphs (a)(1) through
(4) of this section.
(1) If you own or operate an existing
affected source and you certify initial
compliance with the PM emissions limit
in § 63.11148(a) based on monitoring
data from the previous month, your
notification of compliance status
required by § 63.9(h) must include this
certification of compliance, signed by a
responsible official: ‘‘This facility
complies with the PM emissions limit in
§ 63.11148(a) based on monitoring data
that were collected during the previous
month.’’
(2) If you conduct a new performance
test to demonstrate initial compliance
with the PM emissions limit in
§ 63.11148(a), your notification of
compliance status required by § 63.9(h)
must include the results of the
performance test, including required
monitoring data.
(3) Your notification of compliance
status required by § 63.9(h) must
include this certification of compliance,
signed by a responsible official, for the
work practice standard in § 63.11148(b):
‘‘This facility complies with the
requirement to operate a secondary gas
system for each smelting vessel and
converting vessel in accordance with
§ 63.11148(b).’’
(4) Your notification of compliance
status required by § 63.9(h) must
include this certification of compliance,
signed by a responsible official, for the
work practice standard in § 63.11148(c):
‘‘This facility complies with the
requirement to capture gases from
operations in the anode refining and
casting department and duct them to a
control device in accordance with
§ 63.11148(c).’’
(b) If you own or operate a new
affected source, you must comply with
the requirements of the General
Provisions (40 CFR part 63, subpart A)
as specified in Table 1 to this subpart
and paragraphs (b)(1) through (3) of this
section.
(1) Your notification of compliance
status required by § 63.9(h) must
include the results of the initial
performance test and monitoring data
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collected during the test that
demonstrate compliance with the
emissions limit in § 63.11149(a).
(2) Your notification of compliance
status required by § 63.9(h) must
include this certification of compliance,
signed by a responsible official, for the
work practice standard in § 63.11149(b):
‘‘This facility complies with the
requirement to operate a secondary gas
system for each smelting vessel and
converting vessel in accordance with
§ 63.11149(b).’’
(3) Your notification of compliance
status required by § 63.9(h) must
include this certification of compliance,
signed by a responsible official, for the
work practice standard in § 63.11149(c):
‘‘This facility complies with the
requirement to capture gases from
operations in the anode refining and
casting department and duct them to a
control device in accordance with
§ 63.11149(c).’’
§ 63.11151
subpart?
What definitions apply to this
Terms used in this subpart are
defined in the CAA, in 40 CFR 63.2, and
in this section as follows:
Anode refining and casting
department means the area at a primary
copper smelter in which anode copper
refining and casting operations are
performed. Emissions sources in the
anode refining and casting department
include anode refining furnaces, anode
shaft furnaces, anode holding furnaces,
and anode casting wheels.
Capture system means the collection
of components used to capture gases
and fumes released from one or more
emissions points and then convey the
captured gas stream to a control device.
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, and fans.
Control device means air pollution
control equipment used to remove PM
from a gas stream.
Converting vessel means a furnace,
reactor, or other type of vessel in which
copper matte is oxidized to form blister
copper.
Copper concentrate means copper ore
that has been beneficiated or treated to
remove waste and increase the copper
content of the treated material.
Copper concentrate dryer means a
vessel in which copper concentrates are
heated in the presence of air to reduce
the moisture content of the material.
Supplemental copper-bearing feed
materials and fluxes may be added or
mixed with the copper concentrates fed
to a copper concentrate dryer.
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Copper concentrate feed means the
mixture of copper concentrate,
secondary copper-bearing materials,
recycled slags and dusts, fluxes, and
other materials blended together for
feeding to the smelting vessel.
Copper matte means a material
predominately composed of copper and
iron sulfides produced by smelting
copper ore concentrates.
Deviation means any instance in
which an affected source subject to this
subpart, or an owner or operator of such
a source:
(1) Fails to meet any requirement or
obligation established by this subpart,
including but not limited to any
emissions limitation or work practice
standard;
(2) Fails to meet any term or condition
that is adopted to implement an
applicable requirement in this subpart
and that is included in the operating
permit for any affected source required
to obtain such a permit; or
(3) Fails to meet any emissions
limitation or work practice standard in
this subpart during startup, shutdown,
or malfunction, regardless of whether or
not such failure is permitted by this
subpart.
Matte drying and grinding plant
means the area at a primary copper
smelter in which wet granulated matte
copper is ground in a mill, dried by
blowing heated air through the mill, and
then separated from the drying air
stream using a control device such as a
baghouse.
Primary copper smelter means any
installation or any intermediate process
engaged in the production of copper
from copper sulfide ore concentrates
through the use of pyrometallurgical
techniques.
Responsible official means
responsible official as defined at 40 CFR
70.2.
Secondary gas system means a
capture system that collects the gases
and fumes released when removing and
transferring molten materials from
smelting vessels and converting vessels
using tapping ports, launders, and other
openings in the vessels. Examples of
molten material include, but are not
limited to: copper matte, slag, and
blister copper.
Smelting vessel means a furnace,
reactor, or other type of vessel in which
copper ore concentrate and fluxes are
melted to form a molten mass of
material containing copper matte and
slag. Other copper-bearing materials
may also be charged to the smelting
vessel.
Work practice standard means any
design, equipment, work practice, or
operational standard, or combination
thereof.
§ 63.11152 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 a State,
local, or tribal agency. If the U.S. EPA
Administrator has delegated authority to
a State, local, or tribal agency, then that
Agency has the authority to implement
and enforce this subpart. You should
contact your U.S. EPA Regional Office
59325
to find out if this subpart is delegated
to a State, local, or tribal agency within
your State.
(b) In delegating implementation and
enforcement authority of this subpart to
a State, local, or tribal agency under 40
CFR part 63, subpart E, the authorities
contained in paragraph (c) of this
section are retained by the
Administrator of the U.S. EPA and are
not transferred to the State, local, or
tribal agency.
(c) The authorities that will not be
delegated to State, local, or tribal
agencies are listed in paragraphs (c)(1)
through (4) of this section.
(1) Approval of an alternative nonopacity emission standard under
§ 63.6(g).
(2) Approval of a major change to a
test method under § 63.7(e)(2)(ii) and (f).
A ‘‘major change to test method’’ is
defined in § 63.90.
(3) Approval of a major change to
monitoring under § 63.8(f). A ‘‘major
change to monitoring’’ is defined in
§ 63.90.
(4) Approval of a major change to
recordkeeping/ reporting under
§ 63.10(f). A ‘‘major change to
recordkeeping/reporting’’ is defined in
§ 63.90.
Tables to Subpart EEEEEE of Part 63
As required in § 63.11150(a) and (b),
you must comply with the requirements
of the NESHAP General Provisions (40
CFR part 63, subpart A) as shown in the
following table.
TABLE 1 TO SUBPART EEEEEE OF PART 63.—APPLICABILITY OF GENERAL PROVISIONS TO SUBPART EEEEEE
Applies to
Subpart
EEEEEE?
Subject
63.1(a)(1), (a)(2), (a)(3), (a)(4), (a)(6),
(a)(10)–(a)(12) (b)(1), (b)(3), (c)(1),
(c)(2), (c)(5), (e).
63.1(a)(5), (a)(7)–(a)(9), (b)(2), (c)(3),
(c)(4), (d).
63.2 ............................................................
63.3 ............................................................
63.4 ............................................................
63.5 ............................................................
sroberts on PROD1PC70 with PROPOSALS
Citation
Applicability ...............................................
Yes.
Reserved ...................................................
No.
Definitions ..................................................
Units and Abbreviations ............................
Prohibited Activities and Circumvention ...
Preconstruction Review and Notification
Requirements.
Compliance with Standards and Maintenance Requirements.
Yes.
Yes.
Yes.
No.
Reserved ...................................................
No.
63.6(a), (b)(1)–(b)(5), (b)(7), (c)(1), (c)(2),
(c)(5),
(e)(1),
(e)(3)(i),
(e)(3)(iii)–
(e)(3)(ix), (f), (g), (i), (j).
63.6(b)(6), (c)(3), (c)(4), (d), (e)(2),
(e)(3)(ii), (h)(3), (h)(5)(iv).
63.6(h)(1)–(h)(4),
(h)(5)(i)–(h)(5)(iii),
(h)(6)–(h)(9).
63.7(a), (e), (f), (g), (h) ..............................
63.7(b), (c) .................................................
63.8(a)(1), (a)(2), (b), (c), (f), (g) ...............
63.8(a)(3) ...................................................
63.8(a)(4) ...................................................
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Yes.
No ............
Performance Testing Requirements .........
Monitoring Requirements ..........................
Reserved ...................................................
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Explanation
Yes.
Yes/No .....
Yes.
No.
No ............
Subpart EEEEEE does not include opacity or visible emissions standards.
Notification of performance tests and
quality assurance program apply to
new sources but not existing sources.
Subpart EEEEEE does not require flares.
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TABLE 1 TO SUBPART EEEEEE OF PART 63.—APPLICABILITY OF GENERAL PROVISIONS TO SUBPART EEEEEE—
Continued
Citation
Applies to
Subpart
EEEEEE?
Subject
63.8(d), (e) .................................................
Yes/No .....
63.9(a), (b)(1), (b)(2), (b)(5), (c), (d),
(h)(1)–(h)(3), (h)(5), (h)(6), (i), (j).
63.9(b)(3), (h)(4) ........................................
63.9(b)(4), (f) ..............................................
63.9(e), (g) .................................................
Notification Requirements .........................
No.
No.
Yes/No .....
63.10(a), (b)(1), (d)(1), (d)(2), (d)(4),
(d)(5), (f).
63.10(b)(2), (b)(3), (c)(1) (c)(5)–(c)(8),
(c)(10)–(c)(15), (e)(1), (e)(2).
Recordkeeping and Reporting Requirements.
63.10(c)(2)–(c)(4), (c)(9) ............................
63.10(d)(3), (e)(4) ......................................
Reserved ...................................................
63.11
63.12
63.13
63.14
63.15
Control Device Requirements ...................
State Authorities and Delegations ............
Addresses .................................................
Incorporations by Reference .....................
Availability of Information and Confidentiality.
Performance Track Provisions ..................
63.16 ..........................................................
5. Part 63 is amended by adding
subpart FFFFFF to read as follows:
Subpart FFFFFF—National Emission
Standards for Hazardous Air Pollutants
for Secondary Copper Smelting Area
Sources
Sec.
Applicability and Compliance Dates
63.11153 Am I subject to this subpart?
63.11154 What are my compliance dates?
Standards and Compliance Requirements
63.11155 What are the standards and
compliance requirements for new
sources?
63.11156 [Reserved]
Other Requirements and Information
63.11157 What General Provisions apply to
this subpart?
63.11158 What definitions apply to this
subpart?
63.11159 Who implements and enforces
this subpart?
Tables to Subpart FFFFFF of Part 63
Table 1 to Subpart FFFFFF of Part
63—Applicability of General Provisions
to Subpart FFFFFF
Applicability and Compliance Dates
§ 63.11153
Am I subject to this subpart?
(a) You are subject to this subpart if
you own or operate a new secondary
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No.
No ............
Yes/No .....
..........................................................
..........................................................
..........................................................
..........................................................
..........................................................
No ............
Yes.
Yes.
Yes.
Yes.
What are my compliance
(a) If you start up a new affected
source on or before [Date of publication
of final rule in the Federal Register],
you must achieve compliance with the
applicable provisions of this subpart not
later than [DATE OF PUBLICATION OF
FINAL RULE IN THE Federal Register].
(b) If you start up a new affected
source after [DATE OF PUBLICATION
OF FINAL RULE IN THE Federal
PO 00000
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Recordkeeping and reporting requirements apply to new sources but not existing sources.
Subpart EEEEE does not contain opacity
or visible emissions standards.
Reporting requirements apply to new
sources but not existing sources.
Subpart EEEEEE does not require flares.
Yes.
copper smelter that is an area source of
hazardous air pollutant (HAP)
emissions. Your secondary copper
smelter is an area source if it does not
emit and does not have the potential to
emit either 10 tons per year (tpy) or
more of any single HAP or 25 tpy or
more of any combination of HAP.
(b) This subpart applies to each new
affected source. The affected source is
each secondary copper smelter. Your
secondary copper smelter is a new
affected source if you commenced
construction or reconstruction of the
affected source before October 6, 2006.
(c) This subpart does not apply to
research and development facilities, as
defined in section 112(c)(7) of the CAA.
(d) If you own or operate an area
source subject to this subpart, you must
obtain a permit under 40 CFR part 70 or
40 CFR part 71.
§ 63.11154
dates?
Requirement for notification of performance test and for use of continuous
monitoring systems apply to new
sources but not existing sources.
Yes.
Yes/No .....
63.10(e)(3) .................................................
sroberts on PROD1PC70 with PROPOSALS
Requirements for quality control program
and performance evaluations apply to
new sources but not existing sources.
Yes.
Reserved ...................................................
Explanation
Register], you must achieve compliance
with the applicable provisions of this
subpart upon startup of your affected
source.
Standards and Compliance
Requirements
§ 63.11155 What are the standards and
compliance requirements for new sources?
(a) You must not discharge to the
atmosphere any gases which contain
particulate matter (PM) in excess of
0.002 grains per dry standard cubic foot
(gr/dscf) from the exhaust vent of any
capture system for a smelting furnace,
melting furnace, or other vessel that
contains molten material and any
capture system for the transfer of molten
material.
(b) For each smelting furnace, melting
furnace, or other vessel that contains
molten material, you must install and
operate a capture system that collects
the gases and fumes from the vessel and
from the transfer of molten material and
convey the collected gas stream to a
control device.
(c) You must prepare and operate at
all times according to a written plan for
the selection, inspection, and
pretreatment of copper scrap to
minimize, to the extent practicable, the
amount of oil and plastics in the scrap
that is charged to the smelting furnace.
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Your plan must include a training
program for scrap inspectors. You must
keep records to demonstrate continuous
compliance with the requirements of
your plan. You must keep a current
copy of your pollution prevention plan
onsite and available for inspection.
(d) You must install, operate, and
maintain a bag leak detection system on
all baghouses used to comply with the
PM emissions limit in paragraph (a) of
this section according to paragraph
(d)(1) of this section, prepare and
operate by a site-specific monitoring
plan according to paragraph (d)(2) of
this section, take corrective action
according to paragraph (d)(3) of this
section, and record information
according to paragraph (d)(4) of this
section.
(1) Each bag leak detection system
must meet the specifications and
requirements in paragraphs (d)(1)(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 milligram per actual
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. The owner or operator
shall continuously record the output
from the bag leak detection system using
electronic or other means (e.g., using a
strip chart recorder or a data logger.)
(iii) The bag leak detection system
must be equipped with an alarm system
that will sound when the system detects
an increase in relative particulate
loading over the alarm set point
established according to paragraph
(d)(1)(iv) of this section, and the alarm
must be located such that it can be
heard by the appropriate plant
personnel.
(iv) In the initial adjustment of the bag
leak detection system, you must
establish, at a minimum, the baseline
output by adjusting the sensitivity
(range) and the averaging period of the
device, the alarm set points, and the
alarm delay time.
(v) Following initial adjustment, you
shall not adjust the averaging period,
alarm set point, or alarm delay time
without approval from the
Administrator or delegated authority
except as provided in paragraph
(d)(1)(vi) of this section.
(vi) Once per quarter, you may adjust
the sensitivity of the bag leak detection
system to account for seasonal effects,
including temperature and humidity,
according to the procedures identified
in the site-specific monitoring plan
required by paragraph (d)(2) of this
section.
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(vii) You must install the bag leak
detection sensor downstream of the
baghouse and upstream of any wet
scrubber.
(viii) Where multiple detectors are
required, the system’s instrumentation
and alarm may be shared among
detectors.
(2) You must develop and submit to
the Administrator or delegated authority
for approval a site-specific monitoring
plan for each bag leak detection system.
You must operate and maintain the bag
leak detection system according to the
site-specific monitoring plan at all
times. For each bag leak detection
system that operates on the triboelectric
effect, the monitoring plan must be
consistent with the recommendations
contained in the ‘‘Fabric Filter Bag Leak
Detection Guidance’’ (EPA–454/R–98–
015) currently available at https://
www.epa.gov/ttn.emc01/cem/tribo.pdf.
Each monitoring plan must describe the
items in paragraphs (d)(2)(i) through (vi)
of this section.
(i) Installation of the bag leak
detection system;
(ii) Initial and periodic adjustment of
the bag leak detection system, including
how the alarm set-point will be
established;
(iii) Operation of the bag leak
detection system, including quality
assurance procedures;
(iv) How the bag leak detection
system will be maintained, including a
routine maintenance schedule and spare
parts inventory list;
(v) How the bag leak detection system
output will be recorded and stored; and
(vi) Corrective action procedures as
specified in paragraph (d)(3) of this
section. In approving the site-specific
monitoring plan, the Administrator or
delegated authority may allow owners
and operators more than 3 hours to
alleviate a specific condition that causes
an alarm if the owner or operator
identifies in the monitoring plan this
specific condition as one that could lead
to an alarm, adequately explains why it
is not feasible to alleviate this specific
condition within 3 hours of the time the
alarm occurs, and demonstrates that the
requested time will ensure alleviation of
this condition as expeditiously as
practicable.
(3) For each bag leak detection
system, you must initiate procedures to
determine the cause of every alarm
within 1 hour of the alarm. Except as
provided in paragraph (d)(2)(vi) of this
section, you must alleviate the cause of
the alarm within 3 hours of the alarm by
taking whatever corrective action(s) are
necessary. Corrective actions may
include, but are not limited to the
following:
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59327
(i) Inspecting the baghouse for air
leaks, torn or broken bags or filter
media, or any other condition that may
cause an increase in particulate
emissions;
(ii) Sealing off defective bags or filter
media;
(iii) Replacing defective bags or filter
media or otherwise repairing the control
device;
(iv) Sealing off a defective baghouse
compartment;
(v) Cleaning the bag leak detection
system probe or otherwise repairing the
bag leak detection system; or
(vi) Shutting down the process
producing the particulate emissions.
(4) You must maintain records of the
information specified in paragraphs
(d)(4)(i) through (iii) of this section for
each bag leak detection system.
(i) Records of the bag leak detection
system output;
(ii) Records of bag leak detection
system adjustments, including the date
and time of the adjustment, the initial
bag leak detection system settings, and
the final bag leak detection system
settings; and
(iii) The date and time of all bag leak
detection system alarms, the time that
procedures to determine the cause of an
alarm were initiated, whether
procedures were initiated within 1 hour
of the alarm, the cause of the alarm, an
explanation of the actions taken, the
date and time the cause of the alarm was
alleviated, and whether the alarm was
alleviated within 3 hours of the alarm.
(e) You must conduct a performance
test to demonstrate initial compliance
with the PM emissions limit within 180
days after startup and report the results
in your notification of compliance
status. You must conduct each PM test
according to § 63.7(e)(1) using the test
methods and procedures in paragraphs
(e)(1) through (5) of this section.
(1) Method 1 or 1A (40 CFR part 60,
appendix A) to select sampling port
locations and the number of traverse
points in each stack or duct. Sampling
sites must be located at the outlet of the
control device (or at the outlet of the
emissions source if no control device is
present) prior to any releases to the
atmosphere.
(2) Method 2, 2A, 2C, 2D, 2F, or 2G
(40 CFR part 60, appendix A) to
determine the volumetric flow rate of
the stack gas.
(3) Method 3, 3A, or 3B (40 CFR part
60, appendix A) to determine the dry
molecular weight of the stack gas. You
may use ANSI/ASME PTC 19.10–1981,
‘‘Flue and Exhaust Gas Analyses
(incorporated by reference—see § 63.14)
as an alternative to EPA Method 3B.
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(4) Method 4 (40 CFR part 60,
appendix A) to determine the moisture
content of the stack gas.
(5) Method 5 (40 CFR part 60,
appendix A) to determine the PM
concentration for negative pressure
baghouses and Method 5D (40 CFR part
60, appendix A) for positive pressure
baghouses. The sampling time and
volume for each run must be at least 60
minutes and 0.85 dry standard cubic
meters (30 dry standard cubic feet). A
minimum of three valid test runs are
needed to comprise a PM performance
test.
(f) You must conduct subsequent
performance tests to demonstrate
compliance with the PM emissions limit
at least once every 5 years.
(g) If you use a control device other
than a baghouse, you must prepare and
submit a monitoring plan to the
Administrator for approval. Each plan
must contain the information in
paragraphs (g)(1) through (5) of this
section.
(1) A description of the device;
(2) Test results collected in
accordance with paragraph (e) of this
section verifying the performance of the
device for reducing PM to the levels
required by this subpart;
(3) Operation and maintenance plan
for the control device (including a
preventative maintenance schedule
consistent with the manufacturer’s
instructions for routine and long-term
maintenance) and continuous
monitoring system.
(4) A list of operating parameters that
will be monitored to maintain
continuous compliance with the
applicable emission limits; and
(5) Operating parameter limits based
on monitoring data collected during the
performance test.
§ 63.11156
[Reserved]
Other Requirements and Information
§ 63.11157 What General Provisions apply
to this subpart?
sroberts on PROD1PC70 with PROPOSALS
(a) If you own or operate a new
affected source, you must comply with
the requirements of the General
Provisions in 40 CFR part 63, subpart A
as specified in Table 1 to this subpart.
(b) Your notification of compliance
status required by § 63.9(h) must
include the results of the initial
performance tests and monitoring data
collected during the test.
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(c) Your notification of compliance
status required by § 63.9(h) must
include this certification of compliance,
signed by a responsible official, for the
work practice standard in § 63.11155(c):
‘‘This facility complies with the
requirement for a written plan for the
selection, inspection, and pretreatment
of copper scrap in accordance with
§ 63.11155(c).’’
(d) Your notification of compliance
status required by § 63.9(h) must
include this certification of compliance,
signed by a responsible official, for the
work practice standard in
§ 63.11155(d)(2): ‘‘This facility has an
approved monitoring plan in
accordance with § 63.11155(d)(2).’’
(e) If you use control devices other
than baghouses, your notification of
compliance status required by § 63.9(h)
must include this certification of
compliance, signed by a responsible
official for the monitoring plan
requirements in § 63.11157(g): ‘‘This
facility has an approved monitoring
plan in accordance with § 63.11157(g).’’
§ 63.11158
subpart?
What definitions apply to this
Terms used in this subpart are
defined in the CAA, in 40 CFR 63.2, and
in this section as follows:
Anode copper means copper that is
cast into anodes and refined in an
electrolytic process to produce high
purity copper.
Capture system means the collection
of components used to capture gases
and fumes released from one or more
emissions points and then convey the
captured gas stream to a control device.
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, and fans.
Melting furnace means any furnace,
reactor, or other type of vessel that heats
solid materials and produces a molten
mass of material.
Secondary copper smelter means a
facility that processes copper scrap in a
blast furnace and converter or that uses
another pyrometallurgical purification
process to produce anode copper from
copper scrap, including low-grade
copper scrap. A facility where recycled
copper scrap or copper alloy scrap is
melted to produce ingots or for direct
PO 00000
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Sfmt 4702
use in a manufacturing process is not a
secondary copper smelter.
Smelting furnace means any furnace,
reactor, or other type of vessel in which
copper scrap and fluxes are melted to
form a molten mass of material
containing copper and slag.
Work practice standard means any
design, equipment, work practice, or
operational standard, or combination
thereof.
§ 63.11159 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 a State,
local, or tribal agency. If the U.S. EPA
Administrator has delegated authority to
a State, local, or tribal agency, then that
Agency has the authority to implement
and enforce this subpart. You should
contact your U.S. EPA Regional Office
to find out if this 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 40
CFR part 63, subpart E, the authorities
contained in paragraph (c) of this
section are retained by the
Administrator of the U.S. EPA and are
not transferred to the State, local, or
tribal agency.
(c) The authorities that will not be
delegated to State, local, or tribal
agencies are listed in paragraphs (c)(1)
through (4) of this section.
(1) Approval of an alternative nonopacity emissions standard under
§ 63.6(g).
(2) Approval of a major change to test
methods under § 63.7(e)(2)(ii) and (f). A
‘‘major change to test method’’ is
defined in § 63.90.
(3) Approval of a major change to
monitoring under § 63.8(f). A ‘‘major
change to monitoring’’ is defined in
§ 63.90.
(4) Approval of a major change to
recordkeeping/reporting under
§ 63.10(f). A ‘‘major change to
recordkeeping/reporting’’ is defined in
§ 63.90.
Tables to Subpart FFFFFF of Part 63
As required in § 63.11157(a), you
must comply with the requirements of
the General Provisions (40 CFR part 63,
subpart A) as shown in the following
table.
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59329
TABLE 1 TO SUBPART FFFFFF OF PART 63.—APPLICABILITY OF GENERAL PROVISIONS TO SUBPART FFFFFF
Citation
Subject
Applies to
Subpart
FFFFFF?
63.1(a)(1), (a)(2), (a)(3), (a)(4), (a)(6),
(a)(10)–(a)(12) (b)(1), (b)(3), (c)(1),
(c)(2), (c)(5), (e).
63.1(a)(5), (a)(7)–(a)(9), (b)(2), (c)(3),
(c)(4), (d).
63.2 ............................................................
63.3 ............................................................
63.4 ............................................................
63.5 ............................................................
Applicability ...............................................
Yes ..........
Reserved ...................................................
No ............
Definitions ..................................................
Units and Abbreviations ............................
Prohibited Activities and Circumvention ...
Preconstruction Review and Notification
Requirements.
Compliance with Standards and Maintenance Requirements.
Yes ..........
Yes ..........
Yes ..........
No ............
Reserved ...................................................
No ............
63.6(a), (b)(1)–(b)(5), (b)(7), (c)(1), (c)(2),
(c)(5),
(e)(3)(i),
(e)(3)(iii)–(e)(3)(ix),
(f),(g), (i), (j).
63.6(b)(6), (c)(3), (c)(4), (d), (e)(2),
(e)(3)(ii), (h)(3), (h)(5)(iv).
63.6(h)(1)–(h)(4),
(h)(5)(i)–(h)(5)(iii),
(h)(6)–(h)(9).
63.7 ............................................................
63.8(a)(1), (a)(2), (b), (f)(1)–(5) .................
63.8(a)(3) ...................................................
63.8(c), (d), (e), (f)(6), (g) ..........................
Yes ..........
No ............
Performance Testing Requirements .........
Monitoring Requirements ..........................
Reserved ...................................................
63.8(a)(4) ...................................................
63.9(a), (b)(1), (b)(2), (b)(5), (c), (d), (e),
(f), (g), (h)(1)–(h)(3), (h)(5), (h)(6),(i), (j).
63.9(b)(3), (h)(4) ........................................
63.9(b)(4) ...................................................
63.9(f) .........................................................
Notification Requirements .........................
Reserved ...................................................
63.9(g) ........................................................
Yes ..........
Yes ..........
No ............
No ............
No ............
Yes ..........
No ............
No ............
No ............
No ............
63.10(a), (b)(2)(i)–(b)(2)(v), (b)(2)(xiv),
(d)(1), (d)(2), (d)(4), (d)(5), (e)(1), (e)(2),
(f).
63.10(c)(2)–(c)(4), (c)(9) ............................
63.10(b)(2)(vi)–(b)(2)(xiii), (c)(1), (c)(5)–
(c)(14), (e)(1)–(e)(2), (e)(4).
63.10(d)(3) .................................................
Recordkeeping and Reporting Requirements.
Control Device Requirements ...................
State Authorities and Delegations ............
Addresses .................................................
Incorporations by Reference .....................
Availability of Information and Confidentiality.
Performance Track Provisions ..................
6. Part 63 is amended by adding
subpart GGGGGG to read as follows:
Subpart GGGGGG—National Emission
Standards for Hazardous Air Pollutants
for Primary Nonferrous Metals Area
Sources—Zinc, Cadmium, and
Beryllium
Yes ..........
No ............
Yes ..........
Yes ..........
Yes ..........
Yes ..........
63.11163 What are the standards and
compliance requirements for new
sources?
63.11164 What General Provisions apply to
primary zinc production facilities?
Primary Beryllium Production Facilities
Applicability and Compliance Dates
63.11160
63.11161
Other Requirements and Information
sroberts on PROD1PC70 with PROPOSALS
Am I subject to this subpart?
What are my compliance dates?
Primary Zinc Production Facilities
63.11162 What are the standards and
compliance requirements for existing
sources?
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Subpart FFFFFF does not include opacity
or visible emissions standards.
Subpart FFFFFF does not require a continuous monitoring system.
63.11167 What definitions apply to this
subpart?
63.11168 Who implements and enforces
this subpart?
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Subpart FFFFFF does not require a continuous monitoring system.
Subpart FFFFFF does not include opacity
or visible emissions standards.
Subpart FFFFFF does not require flares.
Yes ..........
63.11165 What are the standards and
compliance requirements for new and
existing sources?
63.11166 What General Provisions apply to
primary beryllium production facilities?
Sec.
Subpart FFFFFF does not require a continuous monitoring system.
Subpart FFFFFF does not require flares.
No ............
No ............
63.16 ..........................................................
Subpart FFFFFF does not include opacity
or visible emissions standards.
Yes ..........
Reserved ...................................................
63.10(e)(3) .................................................
63.11 ..........................................................
63.12 ..........................................................
63.13 ..........................................................
63.14 ..........................................................
63.15 ..........................................................
Explanation
Applicability and Compliance Dates
§ 63.11160
Am I subject to this subpart?
(a) You are subject to this subpart if
you own or operate a primary zinc
production facility or primary beryllium
production facility that is an area source
of hazardous air pollutant (HAP)
emissions. Your primary zinc or
primary beryllium production facility is
an area source if it does not emit and
does not have the potential to emit
either 10 tons per year (tpy) or more of
any single HAP or 25 tpy or more of any
combination of HAP.
(b) The affected source is each
existing or new primary zinc production
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facility or primary beryllium production
facility.
(1) An affected source is existing if
you commenced construction or
reconstruction of the affected source
before October 6, 2006.
(2) An affected source is new if you
commenced construction or
reconstruction of the affected source on
or after October 6, 2006.
(c) If you own or operate a new or
existing affected source, you must
obtain a permit under 40 CFR part 70 or
71.
§ 63.11161
dates?
What are my compliance
(a) If you have an existing affected
source, you must achieve compliance
with applicable provisions in this
subpart by [DATE OF PUBLICATION
OF THE FINAL RULE IN THE Federal
Register]. If you startup a new sintering
machine at an existing affected source
after [DATE OF PUBLICATION OF THE
FINAL RULE IN THE Federal Register],
you must achieve compliance with the
applicable provisions in this subpart not
later than 180 days after startup.
(b) If you have a new affected source,
you must achieve compliance with
applicable provisions in this subpart
according to the dates in paragraphs
(b)(1) and (2) of this section.
(1) If you startup a new affected
source on or before [DATE OF
PUBLICATION OF FINAL RULE IN
THE Federal Register], you must
achieve compliance with applicable
provisions in this subpart not later than
[DATE OF PUBLICATION OF THE
FINAL RULE IN THE Federal Register].
(2) If you startup a new affected
source after [DATE OF PUBLICATION
OF THE FINAL RULE IN THE Federal
Register], you must achieve compliance
with applicable provisions in this
subpart upon initial startup.
Primary Zinc Production Facilities
sroberts on PROD1PC70 with PROPOSALS
§ 63.11162 What are the standards and
compliance requirements for existing
sources?
(a) You must exhaust the off-gases
from each roaster to a particulate matter
(PM) control device and to a sulfuric
acid plant, including during the
charging of the roaster.
(b) You must not discharge to the
atmosphere any gases which contain PM
in excess of the emissions limits in
paragraphs (b)(1) through (5) of this
section.
(1) 0.93 pound per hour (lb/hr) from
the exhaust vent of a zinc cathode
melting furnace.
(2) 0.1 lb/hr from the exhaust vent of
a furnace that melts zinc dust, zinc
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chips, and/or other materials containing
zinc.
(3) 0.228 lb/hr from the vent for the
combined exhaust from a furnace
melting zinc scrap and an alloy furnace.
(4) 0.014 grains per dry standard
cubic foot (gr/dscf) from the exhaust
vent of an anode casting furnace.
(5) 0.015 gr/dscf from the exhaust
vent of a cadmium melting furnace.
(c) You must establish an operating
range for pressure drop for each
baghouse applied to a furnace subject to
an emissions limit in paragraph (b) of
this section based on the minimum and
maximum values recorded during a
performance test that demonstrates
compliance with the applicable PM
emissions limit. Alternatively, you may
use an operating range that has been
previously established and approved by
your permitting authority within the
past 5 years. You must monitor the
pressure drop daily, maintain the
pressure drop for each baghouse within
the established operating range, and
record the pressure drop measurement
in a daily log. You must perform routine
maintenance on each baghouse and
record maintenance activities in a
baghouse maintenance log. Baghouse
maintenance logs must include, but are
not limited to, inspections, criteria for
changing bag filters, and dates on which
the bag filters are replaced. Both logs
must be maintained in a suitable
permanent form and kept available for
inspection.
(d) If you own or operate a sintering
machine at your facility, you must
comply with the PM emissions limit in
40 CFR 60.172(a) and the opacity
emissions limit in 40 CFR 60.174(a) for
that sintering machine.
(e) If you own or operate a sintering
machine at your facility, you must
install and operate a continuous opacity
monitoring system (COMS) for each
sintering machine according to the
requirements in 40 CFR 60.175(a). Each
COMS must meet Performance
Specification 1 (40 CFR part 60,
appendix B).
(f) For each furnace at your facility,
you must demonstrate initial
compliance with the applicable PM
emissions limit in paragraph (b) of this
section based on the results of a
performance test for that furnace. If you
own or operate a sintering machine, you
must also demonstrate initial
compliance with the PM and opacity
emissions limits in paragraph (d) of this
section based on the results of a
performance test for that sintering
machine.
(1) You may certify initial compliance
for a furnace (and sintering machine, if
applicable) based on the results of a
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previous performance test conducted
during the past 5 years.
(2) If you have not conducted a
performance test to demonstrate
compliance with the applicable
emissions limits during the past 5 years,
you must conduct a performance test
within 180 days of your compliance
date and report the results in your
notification of compliance status.
(3) You must conduct each PM test for
a furnace according to § 63.7(e)(1) using
the test methods and procedures in
paragraphs (f)(3)(i) through (v) of this
section.
(i) Method 1 or 1A (40 CFR part 60,
appendix A) to select sampling port
locations and the number of traverse
points in each stack or duct. Sampling
sites must be located at the outlet of the
control device (or at the outlet of the
emissions source if no control device is
present) prior to any releases to the
atmosphere.
(ii) Method 2, 2A, 2C, 2D, 2F, or 2G
(40 CFR part 60, appendix A) to
determine the volumetric flow rate of
the stack gas.
(iii) Method 3, 3A, or 3B (40 CFR part
60, appendix A) to determine the dry
molecular weight of the stack gas. You
may use ANSI/ASME PTC 19.10–1981,
‘‘Flue and Exhaust Gas Analyses’’
(incorporated by reference—see § 63.14)
as an alternative to EPA Method 3B.
(iv) Method 4 (40 CFR part 60,
appendix A) to determine the moisture
content of the stack gas.
(v) Method 5 (40 CFR part 60,
appendix A) to determine the PM
concentration for a negative pressure
baghouse, Method 5D (40 CFR part 60,
appendix A) for a positive pressure
baghouse, or an alternative method
previously approved by your permitting
authority. A minimum of three valid test
runs are needed to comprise a PM
performance test.
(4) You must conduct each PM test for
a sintering machine according to
§ 63.7(e)(1) and 40 CFR 60.176(b)(1)
using the test methods in paragraph
(f)(3) of this section. You must
determine the PM concentration using
EPA Method 5 (40 CFR part 60,
appendix A). You may use ANSI/ASME
PTC 19.10–1981, ‘‘Flue and Exhaust Gas
Analyses’’ (incorporated by reference—
see § 63.14) as an alternative to EPA
Method 3B.
(5) You must conduct each opacity
test for a sintering machine according to
the requirements in § 63.6(h)(7). You
must determine the opacity of emissions
using EPA Method 9 (40 CFR part 60,
appendix A).
(g) For each furnace subject to an
emissions limit in paragraph (b) of this
section, you must conduct subsequent
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performance tests according to the
requirements in paragraph (f)(3) of this
section to demonstrate compliance with
the applicable PM emissions limit for
the furnace every 5 years.
(h) You must submit a notification to
your permitting authority of any
deviation from the requirements of this
subpart within 30 days after the
deviation. The notification must
describe the probable cause of the
deviation and any corrective actions or
preventative measures taken.
(i) You must submit semiannual
monitoring reports to your permitting
authority containing the results for all
monitoring required by this subpart. All
deviations that occur during the
reporting period must be clearly
identified.
(j) You must keep records of all
required monitoring data and support
information. Support information
includes all calibration and
maintenance records and all original
strip chart recordings for continuous
monitoring instrumentation and copies
of all reports required by this subpart.
sroberts on PROD1PC70 with PROPOSALS
§ 63.11163 What are the standards and
compliance requirements for new sources?
(a) You must exhaust the off-gases
from each roaster to a PM control device
and to a sulfuric acid plant, including
the charging of the roaster.
(b) You must not discharge to the
atmosphere any gases which contain PM
in excess of the emissions limits in
paragraphs (b)(1) through (3) of this
section.
(1) 0.005 gr/dscf from the exhaust
vent of a zinc cathode melting furnace;
scrap zinc melting furnace; furnace
melting zinc dust, zinc chips, and other
materials containing zinc; and alloy
melting furnace.
(2) 0.014 gr/dscf from the exhaust
vent of an anode casting furnace.
(3) 0.015 gr/dscf from the exhaust
vent of a cadmium melting furnace.
(c) For each melting furnace, you
must install and operate a capture
system that collects gases and fumes
from the melting furnace and from the
transfer of molten materials and conveys
the collected gases to a control device.
(d) You must install, operate, and
maintain a bag leak detection system on
all baghouses used to comply with the
PM emissions limit in paragraph (b) of
this section according to paragraph
(d)(1) of this section, prepare and
operate by a site-specific monitoring
plan according to paragraph (d)(2) of
this section, take corrective action
according to paragraph (d)(3) of this
section, and record information
according to paragraph (d)(4) of this
section.
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(1) Each bag leak detection system
must meet the specifications and
requirements in paragraphs (d)(1)(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 milligram per actual
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. The owner or operator
shall continuously record the output
from the bag leak detection system using
electronic or other means (e.g., using a
strip chart recorder or a data logger.)
(iii) The bag leak detection system
must be equipped with an alarm system
that will sound when the system detects
an increase in relative particulate
loading over the alarm set point
established according to paragraph
(d)(1)(iv) of this section, and the alarm
must be located such that it can be
heard by the appropriate plant
personnel.
(iv) In the initial adjustment of the bag
leak detection system, you must
establish, at a minimum, the baseline
output by adjusting the sensitivity
(range) and the averaging period of the
device, the alarm set points, and the
alarm delay time.
(v) Following initial adjustment, you
shall not adjust the averaging period,
alarm set point, or alarm delay time
without approval from the
Administrator or delegated authority
except as provided in paragraph
(d)(1)(vi) of this section.
(vi) Once per quarter, you may adjust
the sensitivity of the bag leak detection
system to account for seasonal effects,
including temperature and humidity,
according to the procedures identified
in the site-specific monitoring plan
required by paragraph (d)(2) of this
section.
(vii) You must install the bag leak
detection sensor downstream of the
baghouse and upstream of any wet
scrubber.
(viii) Where multiple detectors are
required, the system’s instrumentation
and alarm may be shared among
detectors.
(2) You must develop and submit to
the Administrator or delegated authority
for approval a site-specific monitoring
plan for each bag leak detection system.
You must operate and maintain the bag
leak detection system according to the
site-specific monitoring plan at all
times. For each bag leak detection
system that operates on the triboelectric
effect, the monitoring plan must be
consistent with the recommendations
contained in the ‘‘Fabric Filter Bag Leak
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Detection Guidance’’ (EPA–454/R–98–
015) currently available at https://
www.epa.gov/ttn.emc01/cem/tribo.pdf.
Each monitoring plan must describe the
items in paragraphs (d)(2)(i) through (vi)
of this section.
(i) Installation of the bag leak
detection system;
(ii) Initial and periodic adjustment of
the bag leak detection system, including
how the alarm set-point will be
established;
(iii) Operation of the bag leak
detection system, including quality
assurance procedures;
(iv) How the bag leak detection
system will be maintained, including a
routine maintenance schedule and spare
parts inventory list;
(v) How the bag leak detection system
output will be recorded and stored; and
(vi) Corrective action procedures as
specified in paragraph (d)(3) of this
section. In approving the site-specific
monitoring plan, the Administrator or
delegated authority may allow owners
and operators more than 3 hours to
alleviate a specific condition that causes
an alarm if the owner or operator
identifies in the monitoring plan this
specific condition as one that could lead
to an alarm, adequately explains why it
is not feasible to alleviate this condition
within 3 hours of the time the alarm
occurs, and demonstrates that the
requested time will ensure alleviation of
this condition as expeditiously as
practicable.
(3) For each bag leak detection
system, you must initiate procedures to
determine the cause of every alarm
within 1 hour of the alarm. Except as
provided in paragraph (d)(2)(vi) of this
section, you must alleviate the cause of
the alarm within 3 hours of the alarm by
taking whatever corrective action(s) are
necessary. Corrective actions may
include, but are not limited to the
following:
(i) Inspecting the baghouse for air
leaks, torn or broken bags or filter
media, or any other condition that may
cause an increase in particulate
emissions;
(ii) Sealing off defective bags or filter
media;
(iii) Replacing defective bags or filter
media or otherwise repairing the control
device;
(iv) Sealing off a defective baghouse
compartment;
(v) Cleaning the bag leak detection
system probe or otherwise repairing the
bag leak detection system; or
(vi) Shutting down the process
producing the particulate emissions.
(4) You must maintain records of the
information specified in paragraphs
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(d)(4)(i) through (iii) of this section for
each bag leak detection system.
(i) Records of the bag leak detection
system output;
(ii) Records of bag leak detection
system adjustments, including the date
and time of the adjustment, the initial
bag leak detection system settings, and
the final bag leak detection system
settings; and
(iii) The date and time of all bag leak
detection system alarms, the time that
procedures to determine the cause of the
alarm were initiated, if procedures were
initiated within 1 hour of the alarm, the
cause of the alarm, an explanation of the
actions taken, the date and time the
cause of the alarm was alleviated, and
if the alarm was alleviated within 3
hours of the alarm.
(e) If there is a sintering machine at
your primary zinc production facility,
you must comply with the PM
emissions limit in 40 CFR 60.172(a) and
the opacity emissions limit in 40 CFR
60.174(a) for that sintering machine.
(f) If there is a sintering machine at
your primary zinc production facility,
you must install and operate a COMS
for each sintering machine according to
the requirements in 40 CFR 60.175(a).
Each COMS must meet EPA
Performance Specification 1 (40 CFR
part 60, appendix B).
(g) For each furnace (and sintering
machine, if applicable) at your facility,
you must conduct a performance test to
demonstrate initial compliance with
each applicable PM emissions limit for
that furnace (and the PM and opacity
limits for a sintering machine, if
applicable) within 180 days after startup
and report the results in your
notification of compliance status.
(1) You must conduct each PM test for
a furnace according to § 63.7(e)(1) using
the test methods and procedures in
paragraphs (g)(1)(i) through (v) of this
section.
(i) Method 1 or 1A (40 CFR part 60,
appendix A) to select sampling port
locations and the number of traverse
points in each stack or duct. Sampling
sites must be located at the outlet of the
control device (or at the outlet of the
emissions source if no control device is
present) prior to any releases to the
atmosphere.
(ii) Method 2, 2A, 2C, 2D, 2F, or 2G
(40 CFR part 60, appendix A) to
determine the volumetric flow rate of
the stack gas.
(iii) Method 3, 3A, or 3B (40 CFR part
60, appendix A) to determine the dry
molecular weight of the stack gas. You
may use ANSI/ASME PTC 19.10–1981,
‘‘Flue and Exhaust Gas Analyses
(incorporated by reference-see § 63.14)
as an alternative to EPA Method 3B.
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(iv) Method 4 (40 CFR part 60,
appendix A) to determine the moisture
content of the stack gas.
(v) Method 5 (40 CFR part 60,
appendix A) to determine the PM
concentration for negative pressure
baghouses or Method 5D (40 CFR part
60, appendix A) for positive pressure
baghouses. A minimum of three valid
test runs are needed to comprise a PM
performance test.
(2) You must conduct each PM test for
a sintering machine according to
§ 63.7(e)(1) and 40 CFR 60.176(b)(1)
using the test methods in paragraph
(g)(1) of this section. You must
determine the PM concentration using
EPA Method 5 (40 CFR part 60,
appendix A). You may use ANSI/ASME
PTC 19.10–1981, ‘‘Flue and Exhaust Gas
Analyses’’ (incorporated by referencesee § 63.14) as an alternative to EPA
Method 3B.
(3) You must conduct each opacity
test for a sintering machine according to
the requirements in § 63.6(h)(7). You
must determine the opacity of emissions
using EPA Method 9 (40 CFR part 60,
appendix A).
(h) You must conduct subsequent
performance tests according to the
requirements in paragraph (g)(1) of this
section for each furnace subject to an
emissions limit in paragraph (b) of this
section to demonstrate compliance at
least once every 5 years.
(i) If you use a control device other
than a baghouse, you must prepare and
submit a monitoring plan to the
Administrator for approval. Each plan
must contain the information in
paragraphs (i)(1) through (5) of this
section.
(1) A description of the device;
(2) Test results collected in
accordance with paragraph (g) of this
section verifying the performance of the
device for reducing PM and opacity to
the levels required by this subpart;
(3) Operation and maintenance plan
for the control device (including a
preventative maintenance schedule
consistent with the manufacturer’s
instructions for routine and long-term
maintenance) and continuous
monitoring system;
(4) A list of operating parameters that
will be monitored to maintain
continuous compliance with the
applicable emission limits; and
(5) Operating parameter limits based
on monitoring data collected during the
performance test.
63.11164 What General Provisions apply
to primary zinc production facilities?
(a) If you own or operate an existing
affected source, you must comply with
the requirements of the General
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Provisions in 40 CFR part 63, subpart A,
according to Table 1 to this subpart and
paragraphs (a)(1) through (3) of this
section.
(1) Your notification of compliance
status required by § 63.9(h) must
include this certification of compliance,
signed by a responsible official, for the
work practice standards in
§ 63.11162(a): ‘‘This facility complies
with the work practice standards in
§ 63.11162(a).’’
(2) If you certify compliance with the
PM emissions limits in § 63.11162(b)
based on a previous performance test,
your notification of compliance status
required by § 63.9(h) must include this
certification of compliance, signed by a
responsible official: ‘‘This facility
complies with the PM emissions limits
in § 63.11162(b) based on a previous
performance test.’’
(3) If you conduct a new performance
test to demonstrate compliance with the
PM emissions limits for a furnace in
§ 63.11162(b), your notification of
compliance status required by § 63.9(h)
must include the results of the
performance test, including required
monitoring data.
(b) If you own or operate a new
affected source, you must comply with
the requirements of the General
Provisions (40 CFR part 63, subpart A)
as provided in Table 1 to this subpart
and paragraphs (b)(1) through (4) of this
section.
(1) Your notification of compliance
status required in § 63.9(h) must include
the results of the initial performance
tests, including required monitoring
data.
(2) Your notification of compliance
status required by § 63.9(h) must
include this certification of compliance,
signed by a responsible official, for the
work practice standard in § 63.11163(a):
‘‘This facility complies with the work
practice standards in § 63.11163(a).’’
(3) Your notification of compliance
status required by § 63.9(h) must
include this certification of compliance,
signed by a responsible official, for the
capture system requirements in
§ 63.11163(c): ‘‘This facility has
installed capture systems according to
§ 63.11163(c).’’
(4) If you use a baghouse that is
subject to the requirements in
§ 63.11163(d), your notification of
compliance status required by § 63.9(h)
must include this certification of
compliance, signed by a responsible
official, for the bag leak detection
system requirements in § 63.11163(d):
‘‘This facility has an approved
monitoring plan in accordance with
§ 63.11163(d).’’
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(5) If you use control devices other
than baghouses, your notification of
compliance status required by § 63.9(h)
must include this certification of
compliance, signed by a responsible
official for the monitoring plan
requirements in § 63.11163(i): ‘‘This
facility has an approved monitoring
plan in accordance with § 63.11163(i).’’
Primary Beryllium Production
Facilities
§ 63.11165 What are the standards and
compliance requirements for new and
existing sources?
You must comply with the
requirements in 40 CFR 61.32 through
40 CFR 61.34 of the National Emission
Standards for Beryllium (40 CFR part
61, subpart C).
§ 63.11166 What General Provisions apply
to primary beryllium production facilities?
(a) You must comply with all of the
requirements of the General Provisions
in 40 CFR part 61, subpart A.
(b) You must comply with the
requirements of the General Provisions
in 40 CFR part 63, subpart A, that are
specified in paragraphs (b)(1) through
(4) of this section.
(1) Section 63.1(a)(1) through (10).
(2) Section 63.1(b) except paragraph
(b)(3), § 63.1(c), and § 63.1(e).
(3) Section 63.5 (preconstruction
review and notification requirements)
except for the references to § 63.6 for
compliance procedures and the
references to § 63.9 for notification
procedures.
(4) Section 63.6(e)(3).
Other Requirements and Information
sroberts on PROD1PC70 with PROPOSALS
§ 63.11167
subpart?
What definitions apply to this
Terms used in this subpart are
defined in the CAA; 40 CFR 60.2;
60.171; 61.02; 61.31; 61.61; 63.2; and in
this section as follows:
Alloy furnace means any furnace used
to melt alloys or to produce zinc that
contains alloys.
Anode casting furnace means any
furnace that melts materials to produce
the anodes used in the electrolytic
process for the production of zinc.
Bag leak detection system means a
system that is capable of continuously
monitoring the relative particulate
matter (dust) loadings in the exhaust of
a baghouse to detect bag leaks and other
conditions that result in increases in
particulate loadings. A bag leak
detection system includes, but is not
limited to, an instrument that operates
on triboelectric, electrodynamic, light
scattering, light transmittance, or other
effect to continuously monitor relative
particulate matter loadings.
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Cadmium melting furnace means any
furnace used to melt cadmium or
produce cadmium oxide from the
cadmium recovered in the zinc
production process.
Capture system means the collection
of equipment used to capture gases and
fumes released from one or more
emissions points and then convey the
captured gas stream to a control device.
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, and fans.
Deviation means any instance in
which an affected source subject to this
subpart, or an owner or operator of such
a source:
(1) Fails to meet any requirement or
obligation established by this subpart,
including but not limited to any
emissions limitation or work practice
standard;
(2) Fails to meet any term or condition
that is adopted to implement an
applicable requirement in this subpart
and that is included in the operating
permit for any affected source required
to obtain such a permit; or
(3) Fails to meet any emissions
limitation or work practice standard in
this subpart during startup, shutdown,
or malfunction, regardless of whether or
not such failure is permitted by this
subpart.
Primary beryllium production facility
means any establishment engaged in the
chemical processing of beryllium ore to
produce beryllium metal, alloy, or
oxide, or performing any of the
intermediate steps in these processes. A
primary beryllium production facility
may also be known as an extraction
plant.
Primary zinc production facility
means an installation engaged in the
production, or any intermediate process
in the production, of zinc or zinc oxide
from zinc sulfide ore concentrates
through the use of pyrometallurgical
techniques.
Responsible official means
responsible official as defined in 40 CFR
70.2.
Roaster means any facility in which a
zinc sulfide ore concentrate charge is
heated in the presence of air to
eliminate a significant portion (more
than 10 percent) of the sulfur contained
in the charge.
Sintering machine means any furnace
in which calcines are heated in the
presence of air to agglomerate the
calcines into a hard porous mass called
sinter.
Sulfuric acid plant means any facility
producing sulfuric acid from the sulfur
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59333
dioxide (SO2) in the gases from the
roaster.
Work practice standard means any
design, equipment, work practice, or
operational standard, or combination
thereof.
Zinc cathode melting furnace means
any furnace used to melt the pure zinc
from the electrolytic process.
§ 63.11168 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 a State,
local, or tribal agency. If the U.S. EPA
Administrator has delegated authority to
a State, local, or tribal agency, then that
Agency has the authority to implement
and enforce this subpart. You should
contact your U.S. EPA Regional Office
to find out if this subpart is delegated
to your State, local, or tribal agency.
(b) In delegating implementation and
enforcement authority of this subpart to
a State, local, or tribal agency under 40
CFR part 63, subpart E, the authorities
contained in paragraphs (c) and (d) of
this section are retained by the
Administrator of the U.S. EPA and are
not transferred to the State, local, or
tribal agency.
(c) For primary zinc production
facilities subject to this subpart, the
authorities that will not be delegated to
State, local, or tribal agencies are listed
in paragraphs (c)(1) through (5) of this
section.
(1) Approval of an alternative nonopacity emissions standard under
§ 63.6(g).
(2) Approval of an alternative opacity
emissions standard under § 63.6(h)(9).
(3) Approval of a major change to test
methods under § 63.7(e)(2)(ii) and (f). A
‘‘major change to test method’’ is
defined in § 63.90.
(4) Approval of a major change to
monitoring under § 63.8(f). A ‘‘major
change to monitoring’’ is defined in
§ 63.90.
(5) Approval of a major change to
recordkeeping/reporting under
§ 63.10(f). A ‘‘major change to
recordkeeping/reporting’’ is defined in
§ 63.90.
(d) For primary beryllium
manufacturing facilities subject to this
subpart, the authorities that will not be
delegated to State, local, or tribal
agencies are listed in paragraphs (d)(1)
through (4) of this section.
(1) Approval of an alternative nonopacity emissions standard under 40
CFR 61.12(d).
(2) Approval of a major change to test
methods under 40 CFR 61.13(h). A
‘‘major change to test method’’ is
defined in § 63.90.
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(3) Approval of a major change to
monitoring under 40 CFR 61.14(g). A
‘‘major change to monitoring’’ is defined
in § 63.90.
(4) Approval of a major change to
recordkeeping/reporting under 40 CFR
61.10. A ‘‘major change to
recordkeeping/reporting’’ is defined in
§ 63.90.
Tables to Subpart GGGGGG of Part 63
As required in § 63.11164(a) and (b),
you must comply with the requirements
of the NESHAP General Provisions (40
CFR part 63, subpart A) as shown in the
following table.
TABLE 1 TO SUBPART GGGGGG OF PART 63.—APPLICABILITY OF GENERAL PROVISIONS TO PRIMARY ZINC PRODUCTION
AREA SOURCES
Applies to
Subpart
GGGGGG
Citation
Subject
63.1(a)(1), (a)(2), (a)(3), (a)(4), (a)(6),
(a)(10)–(a)(12), (b)(1), (b)(3), (c)(1),
(c)(2), (c)(5), (e).
63.1(a)(5), (a)(7)–(a)(9), (b)(2), (c)(3),
(c)(4), (d).
63.2 ............................................................
63.3 ............................................................
63.4 ............................................................
63.5 ............................................................
Applicability ...............................................
Yes.
Reserved ...................................................
No.
Yes.
Yes.
Yes.
No.
63.6(a), (b)(1)–(b)(5), (b)(7), (c)(1), (c)(2),
(c)(5),
(e)(1),
(e)(3)(i),
(e)(3)(iii)–
(e)(3)(ix), (f), (g), (h)(1), (h)(2),(h)(5)–
(h)(9), (i), (j).
63.6(b)(6), (c)(3), (c)(4), (d), (e)(2),
(e)(3)(ii), (h)(3), (h)(5)(iv).
63.7(a), (e), (f), (g), (h) ..............................
63.7(b), (c) .................................................
Definitions ..................................................
Units and Abbreviations ............................
Prohibited Activities and Circumvention ...
Preconstruction Review and Notification
Requirements.
Compliance with Standards and Maintenance Requirements.
Reserved ...................................................
No.
Performance Testing Requirements .........
Yes.
Yes/No .....
63.8(a)(1), (a)(2), (b), (c), (f), (g) ...............
Monitoring Requirements ..........................
Yes ..........
63.8(a)(3) ...................................................
63.8(a)(4) ...................................................
Reserved ...................................................
No.
No ............
63.8(d), (e) .................................................
Yes.
Yes/No .....
63.9(a), (b)(1), (b)(2), (b)(5), (c), (d), (f),
(g), (h)(1)–(h)(3), (h)(5), (h)(6), (i), (j).
Notification Requirements .........................
Yes/No .....
63.9(b)(3), (h)(4) ........................................
63.9(b)(4) ...................................................
63.10(a), (b)(1), (b)(2)(i)–(v), (d)(4),
(d)(5)(i), (f).
63.10(b)(2), (b)(3), (c)(1), (c)(5)–(c)(8),
(c)(10)–(c)(15), (d)(1)–(d)(3), (d)(5)(ii),
(e)(1), (e)(2), (e)(4).
63.10(c)(2)–(c)(4), (c)(9) ............................
63.10(e)(3) .................................................
Reserved ...................................................
Notification of performance tests and
quality assurance program apply to
new sources but not existing sources.
Requirements in § 63.6(c)(4)(i)–(ii), (c)(5),
(c)(6), (d), (e), (f)(6), and (g) apply if a
COMS is used.
Subpart GGGGGG does not require
flares.
Requirements for quality control program
and performance evaluations apply to
new sources but not existing sources.
Notification of performance tests and
opacity or visible emissions observations apply to new sources but not existing sources.
No.
No.
Yes.
Recordkeeping and Reporting Requirements.
Yes/No .....
Reserved ...................................................
No.
Yes/No .....
63.11 ..........................................................
Control Device Requirements ...................
No ............
63.12
63.13
63.14
63.15
State Authorities and Delegations ............
Addresses .................................................
Incorporations by Reference .....................
Availability of Information and Confidentiality.
Performance Track Provisions ..................
Recordkeeping and reporting requirements apply to new sources but not existing sources.
Reporting requirements apply to new
sources but not existing sources
Subpart GGGGGG does not require
flares.
Yes.
Yes.
Yes.
Yes.
..........................................................
..........................................................
..........................................................
..........................................................
63.16 ..........................................................
sroberts on PROD1PC70 with PROPOSALS
Explanation
Yes.
[FR Doc. 06–8434 Filed 10–5–06; 8:45 am]
BILLING CODE 6560–50–P
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17:35 Oct 05, 2006
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Agencies
[Federal Register Volume 71, Number 194 (Friday, October 6, 2006)]
[Proposed Rules]
[Pages 59302-59334]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-8434]
[[Page 59301]]
-----------------------------------------------------------------------
Part IV
Environmental Protection Agency
-----------------------------------------------------------------------
40 CFR Part 63
National Emission Standards for Hazardous Air Pollutants for Area
Sources: Polyvinyl Chloride and Copolymers Production, Primary Copper
Smelting, Secondary Copper Smelting, and Primary Nonferrous Metals--
Zinc, Cadmium, and Beryllium; Proposed Rule
Federal Register / Vol. 71, No. 194 / Friday, October 6, 2006 /
Proposed Rules
[[Page 59302]]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 63
[EPA-HQ-OAR-2006-0510; FRL-8226-8]
RIN 2060-AN45
National Emission Standards for Hazardous Air Pollutants for Area
Sources: Polyvinyl Chloride and Copolymers Production, Primary Copper
Smelting, Secondary Copper Smelting, and Primary Nonferrous Metals--
Zinc, Cadmium, and Beryllium
AGENCY: Environmental Protection Agency (EPA).
ACTION: Proposed rules.
-----------------------------------------------------------------------
SUMMARY: EPA is proposing national emission standards for hazardous air
pollutants (NESHAP) for four area source categories. The proposed
NESHAP reflect EPA's determination that existing facilities in three of
these categories are well controlled and that the emission control
devices and work practices at these facilities represent the generally
available control technology (GACT) for these source categories. For
secondary copper smelting, we are proposing NESHAP for new area sources
because there is not, and never will be, any existing source in this
category.
DATES: Comments must be received on or before November 6, 2006 unless a
public hearing is requested by October 16, 2006. If a hearing is
requested on the proposed rules, written comments must be received by
November 20, 2006.
Public Hearing. If anyone contacts EPA requesting to speak at a
public hearing concerning the proposed rules by October 16, 2006, we
will hold a public hearing on October 23, 2006. If you are interested
in attending the public hearing, contact Ms. Pamela Garrett at (919)
541-7966 to verify that a hearing will be held.
ADDRESSES: Submit your comments, identified by Docket ID No. EPA-HQ-
OAR-2006-0510, by one of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the on-line instructions for submitting comments.
E-mail: a-and-r-docket@epa.gov.
Fax: (202) 566-1741.
Mail: National Emission Standards for Hazardous Air
Pollutants for Four Area Source Categories, Docket No. EPA-HQ-OAR-2006-
0510, Environmental Protection Agency, EPA Docket Center, Mailcode
6102T, 1200 Pennsylvania Ave., NW., Washington, DC 20460. Please
include a total of two copies. In addition, please mail a copy of your
comments on the information collection provisions to the Office of
Information and Regulatory Affairs, Office of Management and Budget
(OMB), Attn: Desk Officer for EPA, 725 17th St., NW., Washington, DC
20503.
Hand Delivery: EPA Docket Center, Public Reading Room, EPA
West, Room B102, 1301 Constitution Ave., NW., Washington, DC 20460.
Such deliveries are only accepted during the Docket's normal hours of
operation, and special arrangements should be made for deliveries of
boxed information. Note: The EPA Docket Center suffered damage due to
flooding during the last week of June 2006. The Docket Center is
continuing to operate. However, during the cleanup, there will be
temporary changes to Docket Center telephone numbers, addresses, and
hours of operation for people who wish to make hand deliveries or visit
the Public Reading Room to view documents. Consult EPA's Federal
Register notice at 71 FR 38147 (July 5, 2006) or the EPA Web site at
https://www.epa.gov/epahome/dockets.htm for current information on
docket operations, locations and telephone numbers.
Instructions: Direct your comments to Docket ID No. EPA-HQ-OAR-
2006-0510. EPA's policy is that all comments received will be included
in the public docket without change and may be made available online at
https://www.regulations.gov, including any personal information
provided, unless the comment includes information claimed to be
confidential business information (CBI) or other information whose
disclosure is restricted by statute. Do not submit information that you
consider to be CBI or otherwise protected through www.regulations.gov
or e-mail. The www.regulations.gov Web site is an ``anonymous access''
system, which means EPA will not know your identity or contact
information unless you provide it in the body of your comment. If you
send an e-mail comment directly to EPA without going through
www.regulations.gov, your e-mail address will be automatically captured
and included as part of the comment that is placed in the public docket
and made available on the Internet. If you submit an electronic
comment, EPA recommends that you include your name and other contact
information in the body of your comment and with any disk or CD-ROM you
submit. If EPA cannot read your comment due to technical difficulties
and cannot contact you for clarification, EPA may not be able to
consider your comment. Electronic files should avoid the use of special
characters, any form of encryption, and be free of any defects or
viruses.
Docket: All documents in the docket are listed in the Federal
Docket Management System index at https://www.regulations.gov. Although
listed in the index, some information is not publicly available, e.g.,
CBI or other information whose disclosure is restricted by statute.
Certain other material, such as copyrighted material, is not placed on
the Internet and will be publicly available only in hard copy form.
Publicly available docket materials are available either electronically
through www.regulations.gov or in hard copy at the EPA Docket Center,
Public Reading Room, EPA West, Room B102, 1301 Constitution Ave., NW.,
Washington, DC. The Public Reading Room is open from 8:30 a.m. to 4:30
p.m., Monday through Friday, excluding legal holidays. The telephone
number for the Public Reading Room is (202) 566-1744, and the telephone
number for the Air Docket is (202) 566-1742.
FOR FURTHER INFORMATION CONTACT: Mr. Bob Schell, U.S. EPA, Office of
Air Quality Planning and Standards, Sector Policies and Programs
Division, Metals and Minerals Group (D243-02), Research Triangle Park,
North Carolina 27711, telephone number: (919) 541-4116, fax number
(919) 541-3207, e-mail address: schell.bob@epa.gov.
SUPPLEMENTARY INFORMATION: Outline. The information presented in this
preamble is organized as follows:
I. General Information
A. Does this action apply to me?
B. What should I consider as I prepare my comments to EPA?
C. Where can I get a copy of this document and other related
information?
II. Background Information for Proposed Area Source Standards
III. Proposed NESHAP for Polyvinyl Chloride and Copolymers
Production Area Sources
A. What area source category is affected by the proposed NESHAP?
B. What HAP are emitted from polyvinyl chloride and copolymers
production?
C. What are the proposed requirements for area sources?
D. What is our rationale for selecting the proposed standards
for area sources?
E. What is our rationale for exempting polyvinyl chloride and
copolymers production area sources from the CAA title V permit
requirements?
IV. Proposed NESHAP for Primary Copper Smelting Area Sources
A. What area source category is affected by the proposed NESHAP?
B. What HAP are emitted from primary copper smelters?
C. What are the proposed requirements for area sources?
[[Page 59303]]
D. What is our rationale for selecting the proposed standards
for area sources?
V. Proposed NESHAP for Secondary Copper Smelting Area Sources
A. What area source category is affected by the proposed NESHAP?
B. What HAP are emitted from secondary copper smelters?
C. What are the proposed requirements for area sources?
D. What is our rationale for selecting the proposed standards
for area sources?
VI. Proposed NESHAP for Primary Nonferrous Metals-Zinc, Cadmium, and
Beryllium Area Sources
A. What area source category is affected by the proposed NESHAP?
B. What is primary zinc production and what HAP are emitted?
C. What are the proposed requirements for primary zinc
production area sources?
D. What is our rationale for selecting the proposed standards
for primary zinc production area sources?
E. What is primary beryllium production and what HAP are
emitted?
F. What are the proposed requirements for primary beryllium
production area sources?
G. What is our rationale for selecting the proposed standards
for primary beryllium production area sources?
VII. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory Planning and Review
B. Paperwork Reduction Act
C. Regulatory Flexibility Act
D. Unfunded Mandates Reform Act
E. Executive Order 13132: Federalism
F. Executive Order 13175: Consultation and Coordination with
Indian Tribal Governments
G. Executive Order 13045: Protection of Children from
Environmental Health and Safety Risks
H. Executive Order 13211: Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution, or Use
I. National Technology Transfer Advancement Act
I. General Information
A. Does this action apply to me?
The regulated categories and entities potentially affected by the
proposed standards include:
------------------------------------------------------------------------
NAICS code Examples of regulated
Category \1\ entities
------------------------------------------------------------------------
Industry:
Polyvinyl chloride and 325211....... Area source facilities
copolymers production. that polymerize and
copolymers vinyl
chloride monomer to
produce vinyl
production chloride
and/or copolymer
products.
Primary copper smelting..... 331411....... Area source facilities
that produce copper
from copper sulfide
ore concentrates using
pyrometallurgical
techniques.
Secondary copper smelting... 331423 \2\... Area source facilities
that process smelting
copper scrap in a
blast furnace and
converter or use
another
pyrometallurgical
purification process
to produce anode
copper from copper
scrap, including low-
grade copper scrap.
Primary nonferrous metals - 331419....... Area source facilities
zinc, cadmium, and that produce zinc,
beryllium. zinc oxide, cadmium,
or cadmium oxide from
zinc sulfide ore
concentrates using
pyrometallurgical
techniques and area
source facilities that
produce beryllium
metal, alloy, or oxide
from beryllium ore.
Federal government.......... Not affected.
State/local/tribal Not affected.
government.
------------------------------------------------------------------------
\1\ North American Industry Classification System.
\2\ The proposed rule applies only to secondary copper smelters and does
not apply to copper, brass, and bronze ingot makers or remelters that
may also be included under this NAICS code. There are no existing
secondary copper smelters as defined in the proposed rule.
This table is not intended to be exhaustive, but rather provides a
guide for readers regarding entities likely to be affected by this
action. To determine whether your facility would be regulated by this
action, you should examine the applicability criteria in 40 CFR
63.11140 of subpart DDDDDD (NESHAP for Polyvinyl Chloride and
Copolymers Production Area Sources), 40 CFR 63.11146 of subpart EEEEEE
(NESHAP for Primary Copper Smelting Area Sources), 40 CFR 63.11153 of
subpart FFFFFF (NESHAP for Secondary Copper Smelting Area Sources), or
40 CFR 63.11160 of subpart GGGGGG (NESHAP for Primary Nonferrous
Metals--Zinc, Cadmium, and Beryllium Area Sources). If you have any
questions regarding the applicability of this action to a particular
entity, consult either the air permit authority for the entity or your
EPA regional representative as listed in 40 CFR 63.13 of subpart A
(General Provisions).
B. What should I consider as I prepare my comments to EPA?
Do not submit information containing CBI to EPA through
www.regulations.gov or e-mail. Send or deliver information identified
as CBI only to the following address: Roberto Morales, OAQPS Document
Control Officer (C404-02), U.S. EPA, Office of Air Quality Planning and
Standards, Research Triangle Park, North Carolina 27711, Attention
Docket ID EPA-HQ-OAR-2006-0510. Clearly mark the part or all of the
information that you claim to be CBI. For CBI information in a disk or
CD ROM that you mail to EPA, mark the outside of the disk or CD ROM as
CBI and then identify electronically within the disk or CD ROM the
specific information that is claimed as CBI. In addition to one
complete version of the comment that includes information claimed as
CBI, a copy of the comment that does not contain the information
claimed as CBI must be submitted for inclusion in the public docket.
Information so marked will not be disclosed except in accordance with
procedures set forth in 40 CFR part 2.
C. 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
these proposed actions will also be available on the Worldwide Web
(WWW) through the Technology Transfer Network (TTN). Following
signature, a copy of the proposed actions will be posted on the TTN's
policy and guidance page for newly proposed or promulgated rules at the
following address: https://www.epa.gov/ttn/oarpg/. The TTN provides
information and technology exchange in various areas of air pollution
control.
II. Background Information for Proposed Area Source Standards
Section 112(d) of the Clean Air Act (CAA) requires us to establish
NESHAP for both major and area sources of hazardous air pollutants
(HAP) that are listed for regulation under CAA section 112(c). A major
source is a stationary source that emits or has the potential to emit
10 tons per year (tpy) or more of any HAP or 25 tpy or more of any
combination of HAP. An area source is
[[Page 59304]]
a stationary source that is not a major source (i.e., an area source
does not emit and does not have the potential to emit either 10 tpy or
more of any single HAP or 25 tpy or more of any combination of HAP).
Requirements for area sources are described in CAA sections
112(c)(3) and 112(k). These provisions direct EPA (1) to identify not
less than 30 HAP that present the threat to public health in the
largest number of urban areas and (2) to identify sufficient area
source categories to ensure that sources representing 90 percent or
more of the emissions of each of the 30 ``listed'' HAP (``urban HAP'')
are subject to regulation. We implemented these listing requirements
through the Integrated Urban Air Toxics Strategy (64 FR 38715, July 19,
1999).\1\
---------------------------------------------------------------------------
\1\Since its publication in the Integrated Urban Air Toxics
Strategy in 1999, the area source category list has undergone
several amendments.
---------------------------------------------------------------------------
However, EPA has not completed the required regulatory action for
all of the listed area source categories. Pursuant to CAA section 304,
Sierra Club brought suit in the district court for the District of
Columbia to compel EPA to complete this action (Sierra Club v. U.S.
Environmental Protection Agency, no. 01-1537, DC Cir.). On March 31,
2006, the court issued an order requiring, among other things, that we
complete regulatory action for a specified number of area source
categories every 6 months starting December 15, 2006, and complete
regulatory action of all remaining categories by June 15, 2009. The
order requires that, by December 15, 2006, we complete regulatory
action for four area source categories. The four area source categories
that we have selected to meet this obligation and are therefore subject
of this proposal are as follows: (1) Primary Copper Smelting; (2)
Secondary Copper Smelting; (3) Polyvinyl Chloride and Copolymers
Production; and (4) Primary Nonferrous Metals--Zinc, Cadmium, and
Beryllium.
On June 26, 2002, we amended the area source category list by
adding additional source categories, including Polyvinyl Chloride and
Copolymers Production, Secondary Copper Smelting, and Cadmium Refining
and Cadmium Oxide Production source categories (67 FR 43112, 43113). On
November 22, 2002, we further amended the category list by, among other
things, adding Primary Copper Smelting (67 FR 70427, 70428). We also
expanded the Cadmium Refining and Cadmium Oxide Production source
category to include primary zinc and beryllium production and renamed
the category accordingly as Primary Nonferrous Metals--Zinc, Cadmium,
and Beryllium.
The inclusion of each of the four source categories on the area
source category list is based on data from the CAA section 112(k)
inventory, which represents 1990 urban air data. The Polyvinyl Chloride
and Copolymers Production source category listing was based on vinyl
chloride emissions. The Primary Copper Smelting source category listing
was based on HAP metal emissions (arsenic, cadmium, chromium, lead, and
nickel), while Secondary Copper Smelting was based on HAP emissions of
cadmium, lead, and dioxin. The listing of the Primary Nonferrous
Metals-Zinc, Cadmium, and Beryllium source category was based on
emissions of arsenic, cadmium, lead, manganese, and nickel.
Section 112(k)(3)(B) of the CAA requires that EPA ensure that
sources representing 90 percent of the emissions of each of the 30
urban HAP are subject to standards pursuant to section 112(d). Under
CAA section 112(d)(5), the Administrator may, in lieu of standards
requiring maximum achievable control technology (MACT) under section
112(d)(2), elect to promulgate standards or requirements for area
sources ``which provide for the use of generally available control
technologies [``GACT''] or management practices by such sources to
reduce emissions of hazardous air pollutants.'' Under section
112(d)(5), the Administrator has the discretion to use GACT in lieu of
MACT. Pursuant to section 112(d)(5), I have decided not to issue MACT
standards and concluded that GACT is appropriate for these four source
categories.
Legislative history describes GACT as standards reflecting
application of generally available control technology, that is,
``methods, practices and techniques which are commercially available
and appropriate for application by the sources in the category
considering economic impacts and the technical capabilities of the
firms to operate and maintain the emissions control systems'' (Senate
Report Number 101-228, December 20, 1989). In addition to technical
capabilities of the facilities and availabilities of control measures,
legislative history suggests that we may consider costs and economic
impacts in determining GACT, which is particularly important when
developing regulations for source categories that may have few
establishments and many small businesses, or when determining whether
additional control is necessary for sources with emissions that are
already well controlled as a result of other existing or applicable
standards.
Existing facilities in three of these source categories are
currently well controlled as a result of State and national standards
and permitting requirements for criteria pollutants that obtain co-
control of HAP. There are no existing sources in the secondary copper
smelting source category. New and existing area sources of polyvinyl
chloride (PVC) and copolymer plants are subject to the National
Emission Standard for Vinyl Chloride (40 CFR part 61, subpart F). The
vinyl chloride standard requires that new and existing area sources
also comply with the National Emission Standard for Equipment Leaks
(Fugitive Emission Sources) in 40 CFR part 61, subpart V. New and
existing area sources that process beryllium ore, beryllium, beryllium
oxide, beryllium alloys, or beryllium-containing waste are subject to
the National Emission Standard for Beryllium (40 CFR part 61, subpart
C). One of the two primary zinc production area sources is subject to
the new source performance standard (NSPS) at 40 CFR part 60, subpart
Q, and primary copper smelting area sources are subject to the NSPS at
40 CFR part 60, subpart P. These NSPS, as well as other applicable
Federal and State requirements, are incorporated into and enforced
under these primary zinc production and primary copper smelting area
sources' title V permits.
Except for dioxin emissions from secondary copper smelting, the
urban HAP emissions from the three area source categories for
nonferrous metals are all metal HAP. Under the Federal standards
mentioned above that are applicable to these three categories, we are
able to control the urban metal HAP emissions by controlling emissions
of particulate matter (PM), which provide co-control of the HAP metals
for PM. The Secondary Copper Smelting source category does not have any
existing plants--plants that were operating in 1990 have permanently
closed, and no new plants have started. As discussed in more detail in
sections III through VI of this preamble, we conclude that, with the
exception of secondary copper smelting, GACT is equivalent to the
levels of control that are currently required and being implemented by
sources in the other three categories. Because there is not currently
any, nor is there expected to be any existing source of secondary
copper smelting, we are not proposing a standard for existing sources
but are proposing a standard for new area sources of secondary copper
smelting.
[[Page 59305]]
III. Proposed NESHAP for Polyvinyl Chloride and Copolymers Production
Area Sources
A. What area source category is affected by the proposed NESHAP?
The Polyvinyl Chloride and Copolymers Production area source
category includes facilities that polymerize vinyl chloride monomer
alone or in combination with other materials to produce PVC and
copolymers. Sources in this area source category are currently subject
to the National Emission Standard for Vinyl Chloride (40 CFR part 61,
subpart F). The vinyl chloride standard applies to all new and existing
major and area sources of PVC and copolymer production.
We estimate that there are approximately 28 major sources of PVC
and copolymer production facilities operating in the U.S. Although we
do not know of any existing area sources in this category, we cannot
say conclusively that there are not and never will be any area sources
in this category. Consequently, we are proposing standards for both new
and existing area sources. We are requesting comments on whether there
are or ever will be any area sources in this source category.
B. What HAP are emitted from polyvinyl chloride and copolymers
production?
The resins used to make PVC and copolymer products are produced in
batch reactor processes where vinyl chloride is polymerized with itself
as a homopolymer or copolymerized with varying amounts of vinyl
acetate, ethylene, propylene, vinylidene chloride, or acrylates. The
resulting resins are generally dried into nontoxic powders or granules
that are compounded with auxiliary ingredients and converted into a
variety of plastic end products. These end products can be used in a
large number of applications, including latex paints, coatings,
adhesives, clear plastics, rigid plastics, and flooring.
The urban HAP emitted from PVC and copolymer production is vinyl
chloride, which is used as a primary feedstock. The copolymer
feedstocks (e.g., vinyl acetate and vinylidene chloride) are also HAP
under CAA section 112(b) but are not listed as urban HAP. HAP may be
released from an opening or leak in the process equipment. Residual HAP
(i.e., unreacted vinyl chloride) in the product may also become
airborne.
C. What are the proposed requirements for area sources?
1. Applicability and Compliance Dates
The proposed NESHAP apply to both new and existing PVC and
copolymer plants that are area sources. Because existing area sources,
if there are any, would already be operating subject to emissions
limits and work practice standards that are the same as those in this
proposed NESHAP, we are proposing that owners or operators of existing
sources comply with all the requirements of the area source NESHAP by
[Date of publication of the final rule in the Federal Register]. The
owner or operator of a new source would be required to comply with the
area source NESHAP by [DATE OF PUBLICATION OF THE FINAL RULE IN THE
Federal Register] or at startup, whichever is later.
2. Emissions Limitations and Work Practice Standards
We are proposing to adopt as the NESHAP for the Polyvinyl Chloride
and Copolymer Production area source category 40 CFR part 61, subpart
F. Subpart F establishes numerical emissions limits for reactors;
strippers; mixing, weighing, and holding containers; monomer recovery
systems; emissions sources following the stripper(s); and reactors used
as strippers. Subpart F also establishes both emissions limits and work
practice requirements that apply to discharges from manual vent valves
on a PVC reactor and relief valves in vinyl chloride service, fugitive
emissions sources, and equipment leaks. Subpart F requires a new or
existing source to comply with the requirements at 40 CFR part 61,
subpart V for the control of equipment leaks.
3. Compliance Requirements
We are proposing to include in this proposed NESHAP the monitoring,
testing, recordkeeping, and reporting requirements in 40 CFR part 61,
subpart F. The proposed NESHAP requires a vinyl chloride continuous
emissions monitoring system (CEMS) for the regulated emissions sources
(except for sources following the stripper) and for any control system
to which reactor emissions or fugitive emissions must be ducted. Plants
using a stripper to comply with the NESHAP must also determine the
daily average vinyl chloride concentration for each type of resin. The
proposed NESHAP requires the owner or operator to submit quarterly
reports containing information on emissions or resin concentrations
that exceed the applicable limits. Records are required to demonstrate
compliance, including a daily operating log for each reactor. Plants
also would be required to comply with the testing, monitoring,
recordkeeping, and reporting requirements in the part 61 General
Provisions (40 CFR part 61, subpart A). We are also proposing that the
owner or operator comply with the requirements for startup, shutdown,
and malfunction (SSM) plans and reports in 40 CFR 63.6(e)(3). We have
explicitly identified in the proposed NESHAP the applicable General
Provisions of both 40 CFR parts 61 and 63.
D. What is our rationale for selecting the proposed standards for area
sources?
1. Selection of Proposed Standards
Stripping is the primary control measure used at major sources of
PVC and copolymer production facilities to control HAP emissions and
meet the vinyl chloride emissions limits required by 40 CFR part 61,
subpart F, which applies to both major and area sources in this
category. Stripping at the production stage to recover unreacted
feedstock reduces the air emissions from the product by reducing the
residual HAP in the product. In addition to stripping, other HAP
control measures that may be employed to meet the subpart F standards
include: (1) operating under a closed-vent system with add-on control
(e.g., flare) to incinerate HAP gases not returning to the process, and
(2) minimizing the presence of HAP before opening a reactor or piece of
process equipment containing vinyl chloride monomer and other HAP.
Subpart F also requires facilities to comply with the work practice
standards for ongoing leak detection and repair prescribed in 40 CFR
part 61, subpart V. As shown in major source facilities, these
conventional control techniques and work practices are readily
available and highly effective in controlling vinyl chloride emissions
at PVC and copolymer production facilities. Although we are not aware
of any existing area source, we have no reason to believe that the
conventional control techniques employed at major sources to meet the
emissions limits and work practice standards in subpart F are
infeasible, impractical, or inappropriate for area sources. Therefore,
we have determined that the emissions control requirements at 40 CFR
part 61, subpart F represent GACT for new and existing sources in the
Polyvinyl Chloride and Copolymer Production area source category.
[[Page 59306]]
2. Selection of Proposed Compliance Requirements
We have reviewed the compliance requirements in the vinyl chloride
standard and part 61 General Provisions applicable to this proposed
NESHAP and concluded that these requirements are sufficient to ensure
compliance with the proposed emissions limits and work practice
standards. Therefore, we are including the part 61, subpart F
performance test, monitoring requirements, and recordkeeping
requirements in this proposed rule.
The General Provisions applicable to the subpart F standard (40 CFR
part 61, subpart A), are necessary for effective application of the
subpart F standard and are therefore incorporated into this proposed
rule as well. We are also incorporating certain provisions in the
General Provisions of part 63, subpart A to address aspects of this
proposed rule not covered by the part 61 General Provisions.
Specifically, we need to incorporate certain provisions in Sec. Sec.
63.1 and 63.5 of the part 63 General Provisions which delineate
applicability, construction, and reconstruction. However, we are not
applying provisions within 40 CFR 63.1 and 63.5 that are already
covered by part 61 General Provisions. We are proposing to apply the
provisions in 40 CFR 63.1(a) except for the provisions in 40 CFR
63.1(a)(11) and (12) regarding notices, time periods, and postmarks; 40
CFR 63.1(b) except paragraph (b)(3); 40 CFR 63.1(c); 40 CFR 63.1(e);
and 40 CFR 63.5 except for the references to 40 CFR 63.6 for compliance
procedures and the references to 40 CFR 63.9 for notification
procedures. Because the part 61 General Provisions do not include
requirements for SSM plans and reports, we are also proposing to
require the owner or operator of a new or existing area source to
comply with the SSM requirements in 40 CFR 63.6(e)(3) except for the
requirement in 40 CFR 63.6(e)(3)(ix) to include the SSM provisions in
the title V permit.
E. What is our rationale for exempting polyvinyl chloride and
copolymers production area sources from the CAA title V permit
requirements?
Section 502(a) of the CAA provides that EPA may exempt one or more
area sources from the requirements of title V if EPA finds that
compliance with such requirements is ``impracticable, infeasible, or
unnecessarily burdensome'' on such area sources. EPA must determine
whether to exempt an area source from title V at the time we issue the
relevant section 112 standard (40 CFR 70.3(b)(2)). We are proposing in
this action to exempt PVC and copolymers production area sources from
the requirements of title V. PVC and copolymers production area sources
would not be required to obtain title V permits solely as a function of
being the subject of the proposed NESHAP; however, if they were
otherwise required to obtain title V permits, such requirement(s) would
not be affected by the proposed exemption.
Consistent with the statute, EPA has found that compliance with
title V permitting is ``unnecessarily burdensome'' for PVC and
copolymers production area sources. EPA's inquiry into whether this
criterion was satisfied was based primarily upon consideration of the
following four factors: (1) Whether title V would result in significant
improvements to the compliance requirements that we are proposing for
this area source category; (2) whether title V permitting would impose
a significant burden on these area sources and whether that burden
would be aggravated by any difficulty these sources may have in
obtaining assistance from permitting agencies; (3) whether the costs of
title V permitting for these area sources would be justified, taking
into consideration any potential gains in compliance likely to occur
for such sources; and (4) whether there are implementation and
enforcement programs in place that are sufficient to assure compliance
with this NESHAP without relying on title V permits.
Additionally, EPA also considered, consistent with the guidance
provided by the legislative history of CAA section 502(a),\2\ whether
exempting PVC and copolymers production area sources would adversely
affect public health, welfare or the environment. We first determined
the extent to which these factors were present for this area source
category. We then determined whether those factors collectively
demonstrated that compliance with title V requirements would be
unnecessarily burdensome for PVC and copolymer production area sources.
---------------------------------------------------------------------------
\2\ The legislative histroy of section 502(a) suggests that EPA
should not grant title V exemptions where doing so would adversely
affect public health, welfare, or the environment. (See Chafee-
Baucus Statement of Senate Managers, Environment and Natural
Resources Policy Division 1990 CAA Leg. Hist. 905, Compiled
November, 1993.)
---------------------------------------------------------------------------
The first factor is whether title V would result in significant
improvements to the compliance requirements we are proposing for this
area source category. We looked at the compliance requirements of the
proposed NESHAP to see if they were substantially equivalent to the
monitoring, recordkeeping and reporting requirements of title V (see 40
CFR 70.6 and 71.6) that we believe are important for assuring
compliance with the NESHAP. The purpose of this review was to determine
if title V is ``unnecessary'' to improve compliance with this NESHAP. A
finding that title V would not result in significant improvements to
the compliance requirements in the proposed NESAHP would support a
conclusion that title V permitting is ``unnecessary'' for area sources
in this category. One way that title V may improve compliance is by
requiring monitoring (including recordkeeping designed to serve as
monitoring) to assure compliance with the emission limitations and
control technology requirements imposed in the standard. The authority
for adding new monitoring in the permit is in the ``periodic
monitoring'' provisions of 40 CFR 70.6(a)(3)(i)(B) and 40 CFR
71.6(a)(3)(i)(B), which allow new monitoring to be added to the permit
when the underlying standard does not already require ``periodic
testing or instrumental or noninstrumental monitoring (which may
consist of recordkeeping designed to serve as monitoring).'' In
addition, title V imposes a number of recordkeeping and reporting
requirements that may be important for assuring compliance. These
include requirements for a monitoring report at least every 6 months,
prompt reports of deviations, and an annual compliance certification.
See 40 CFR 70.6(a)(3) and 40 CFR 71.6(a)(3), 40 CFR 70.6(c)(1) and 40
CFR 71.6(c)(1), and 40 CFR 70.6(c)(5) and 40 CFR 71.6(c)(5).
To determine whether title V permits would add significant
compliance requirements to the proposed NESHAP for PVC and copolymer
area sources, we compared the title V monitoring, recordkeeping, and
reporting requirements mentioned above to those requirements in the
proposed NESHAP for the Polyvinyl Chloride and Copolymer Production
area source category, which adopts the compliance requirements in the
National Emission Standard for Vinyl Chloride. See 40 CFR 61.60. We
also reviewed the part 61 compliance requirements (specifically 40 CFR
61.67 through 61.71) applicable to this proposed NESHAP. The proposed
NESHAP would require a vinyl chloride CEMS for the regulated emissions
sources (except for sources following the stripper) and for any control
system to which reactor emissions or fugitive emissions must be ducted.
Plants using a stripper to comply with the NESHAP must also
[[Page 59307]]
determine the daily average vinyl chloride concentration for each type
of resin. Because both the continuous and noncontinuous monitoring
methods required by the proposed NESHAP would provide periodic
monitoring, title V would not add any monitoring to the proposed
NESHAP.
We also considered the extent to which title V could enhance
compliance for area sources through recordkeeping or reporting
requirements, including title V requirements for a 6-month monitoring
report, deviation reports, and an annual compliance certification in 40
CFR 70.6 and 71.6. The proposed NESHAP requires the owner or operator
to submit quarterly reports containing information on emissions or
resin concentrations that exceed the applicable limits. Records are
required to demonstrate compliance, including a daily operating log for
each reactor, all emissions measurements, and leak detection and
repair. The information required in the proposed NESHAP is similar to
the information that must be provided in the deviation reports and
semiannual monitoring reports required under 40 CFR 70.6(a)(3) and 40
CFR 71.6(a)(3). The proposed NESHAP does not require an annual
compliance certification report, which is a requirement of a title V
permit. See 40 CFR 70.5(c)(9)(iii) and 40 CFR 71.6(c)(5)(i). EPA
believes that the annual certification reporting requirement is not a
significant compliance requirement because the quarterly reports are
adequate to ensure compliance.
The monitoring, recordkeeping and reporting requirements in the
proposed NESHAP for the Polyvinyl Chloride and Copolymers Production
area source category are substantially equivalent to such requirements
under title V. Therefore, we conclude that title V would not result in
significant improvements to the compliance requirements we are
proposing for this area source category.
The second factor we considered is whether title V permitting would
impose significant burdens on these area sources and whether that
burden would be aggravated by any difficulty these sources may have in
obtaining assistance from permitting agencies. The information
collection request (ICR) for parts 70 and 71 describes the title V
burdens and costs in the aggregate, and although they do not focus on
area sources, they do describe the various activities undertaken by
title V sources, including area sources, so many of the same burdens
and costs described in the ICR will also apply to area sources. Some
examples of this burden include reading and understanding permit
program guidance and regulations, completing the permit application,
preparing and submitting applications for permit revisions every 5
years, and paying permit fees. We believe that this cost is a
significant burden for these area sources based on our general
assessment of this area source category.
The third factor we considered is whether the costs of title V
permitting for these area sources would be justified, taking into
consideration any potential gains in compliance likely to occur for
such sources. We found above that the costs of title V would be a
significant burden on these area sources. Also, based on our
consideration of factor 1 (described above) and factor 4 (described
below), we did not identify potential gain in compliance with this
proposed NESHAP from title V permitting. Therefore, we conclude that
the costs of title V permitting for this area source category are not
justified.
The fourth factor we considered is whether there are implementation
and enforcement programs in place that are sufficient to assure
compliance with this NESHAP without relying on title V permits. A
conclusion that this criteria can be met would support a conclusion
that Title V permitting is ``unnecessary'' for these area sources. See
70 FR 15254. There are State programs in place to enforce this area
source NESHAP. We believe that these programs are sufficient to assure
compliance with this NESHAP. In addition, EPA retains authority to
enforce this NESHAP anytime under CAA sections 112, 113 and 114. In
light of the above, we conclude that title V permitting is
``unnecessary'' to assure compliance with this NESHAP because the
statutory requirements for implementation and enforcement of this
NESHAP by the delegated States and EPA are sufficient to assure
compliance with this area source NESHAP, in all parts of the U.S.,
without title V permits. In addition, small business assistance
programs required by CAA section 507 may be used to assist area sources
that have been exempted from title V permitting. Also, States and EPA
often conduct voluntary compliance assistance, outreach, and education
programs (compliance assistance programs), which are not required by
statute. These additional programs supplement and enhance the success
of compliance with this area source NESHAP. In light of all of the
above, we conclude that there are implementation and enforcement
programs in place that are sufficient to assure compliance with this
NESHAP without relying on title V permitting.
In addition to evaluating whether compliance with title V
requirements is ``unnecessarily burdensome'', EPA also considered,
consistent with guidance provided by the legislative history of section
502(a), whether exempting PVC and copolymer production area sources
from title V requirements would adversely affect public health,
welfare, or the environment. One of the primary purposes of the title V
permitting program is to clarify, in a single document, the various and
sometimes complex regulations that apply to sources in order to improve
understanding of these requirements and to help sources to achieve
compliance with the requirements. In this case, however, we do not
believe that a title V permit is necessary for us to understand all
requirements applicable to PVC and copolymers production area sources.
To our knowledge, currently the only applicable requirements to these
area sources are 40 CFR part 61, subpart F. This proposal would not add
new requirements to PVC and copolymers production area sources. We have
determined that the subpart F requirements reflect GACT and thus
adopted them in this proposed rule. Furthermore, we do not find subpart
F standards to be very complicated to understand or implement. For
these reasons, we do not find that title V permitting is necessary to
improve understanding of and achieve compliance with these standards.
Therefore, we conclude that exempting these area sources from title V
permitting requirements in this proposed rule would not adversely
affect public health, welfare, or the environment.
Based on the above analysis, we conclude that title V permitting
would be ``unnecessarily burdensome'' for PVC and copolymer production
area sources. We are, therefore, proposing that this area source
category be exempt from title V permitting requirements.
IV. Proposed NESHAP for Primary Copper Smelting Area Sources
A. What area source category is affected by the proposed NESHAP?
1. Source Category Description
Copper metal produced directly from copper ore is referred to as
``primary copper.'' The primary copper smelting source category
includes facilities that produce copper from copper sulfide ore
concentrates using a pyrometallurgical process.
Currently, there are three primary copper smelters operating in the
U.S. Two of these smelters are major sources
[[Page 59308]]
of HAP emissions and are subject to the NESHAP for primary copper
smelters in 40 CFR part 63, subpart QQQ. The third smelter is an area
source and is not subject to the NESHAP in subpart QQQ, which only
applies to major sources.
Each of the three primary copper smelters is located in relatively
close proximity to the copper mines supplying the copper ore. Copper
ore excavated from mines is beneficiated to produce copper ore
concentrate. The ore concentrates are first dried to reduce the
moisture content. The dried concentrate then is blended with fluxes and
secondary copper-bearing materials. This mixture is fed to a flash
smelting furnace where the ore is melted and reacts to produce copper
matte, a molten solution of copper sulfide mixed with iron sulfide.
The copper matte from the smelting furnace is converted to blister
copper (approximately 98 percent pure copper) by oxidization to remove
the sulfur as sulfur dioxide (SO2) gas and the iron as a
ferrous oxide slag. The molten slag from converting is cooled and may
be processed in slag concentrators to remove residual copper before on-
site disposal. The SO2 gases from smelting and converting
are vented to a sulfuric acid plant. Copper converting is conducted as
a batch process in which molten matte is charged to large horizontal,
cylindrical vessels or as a continuous process in which solid matte
granules are fed to a flash smelting furnace-like vessel.
Molten blister copper is transferred from the converting vessel to
an anode furnace for refining to further remove residual impurities and
oxygen. The blister copper is reduced in the anode furnace to remove
oxygen, typically by injecting natural gas and steam to produce a high
purity copper. The molten copper from the anode furnace is poured into
molds to produce solid copper ingots called anodes. The anode copper is
sent to a copper refinery, either on-site or at another location, where
it is further purified using an electrolytic process to obtain the
high-purity copper that is sold as a product.
The overall function of a primary copper smelter, regardless of the
technologies used, is to produce anode copper from copper ore
concentrates. However, there are key differences between how the anode
copper is produced at a smelter using flash copper converting
technology compared to smelters use batch copper converting technology.
These differences allow a smelter using flash copper converting
technology to have inherently lower potential HAP emissions than a
smelter using batch copper converting technology.
2. Existing Sources
The primary copper smelter that is an area source uses flash copper
converting technology. At this smelter, molten copper matte tapped from
a flash smelting furnace is not transferred as molten material directly
to the converting vessel as is performed at the two major source
smelters that use batch copper converting technology. Instead, the
matte is first quenched with water to form solid granules of copper
matte. These matte granules are then ground to a finer texture and fed
to the flash converting furnace. This furnace differs significantly in
design and operation from the cylindrical batch converters operated at
the other U.S. smelters. Also, only one flash converting furnace is
needed at the area source smelter compared to multiple batch copper
converter vessels at the other smelters.
Most of the process fugitive emissions associated with smelters
using batch copper converting do not occur in the flash copper
converting process. There are no crane transfers of molten material in
open ladles between the smelting, converting, and anode refining
departments. In addition, because flash copper converting is conducted
in an enclosed vessel as a continuous process, no process off-gases
escape capture, which occurs during the cyclic rolling-out of the batch
copper converters for charging, skimming, and pouring.
While potential HAP emissions are overall lower from flash copper
converting due to the elimination of emissions points, the blister
copper produced by the continuous flash copper converter may contain
higher levels of residual metal HAP impurities than that produced by
the batch copper converting technology. At the smelter using flash
copper converting, however, the anode furnaces and casting operations
are vented to emissions control equipment that is effective in
controlling metal HAP emissions from these processes that follow the
flash copper converting process.
3. New Sources
Record-high commodity prices for refined copper are motivating
companies to expand copper production capacity in the U.S. and other
countries to meet higher demand. The announcement of several new copper
mine projects in the southwestern U.S. indicates that primary copper
production will be increasing in the foreseeable future. For example,
three copper mine projects currently are planned for development in
southeastern Arizona. Production at two of these mines is planned to
start within the next several years.
Increased copper mine development in the U.S. does not
automatically trigger the building of new primary copper smelters. For
instance, there have been no announcements that new smelters are
planned to be built or would be necessary to process the copper ore
from the new mine developments. The output from these new mines will
probably be processed using the alternative hydrometallurgical process
because of economic and technological advantages. This wet process
involves leaching, solvent extraction, and electrowinning steps instead
of the high temperature smelting and converting steps used for the
pyrometallurgical process.
The hydrometallurgical process is conducted in facilities built
near the mine site. This process is preferable for low copper content
ores because of lower production costs compared to the costs of
smelting and refining the ore. Further, because it is a wet process and
does not use any operations involving high temperatures and the
handling of molten materials, the potential for emission of HAP metals
to the atmosphere is very low. Hydrometallurgical processes are not
included in the Primary Copper Smelting area source category.
Although smelters will not be used in association with the new
mining projects mentioned above, we recognize that the record-high
commodity prices for refined copper may encourage construction of new
primary copper smelters in the U.S. Currently, copper smelting
technologies other than the batch and flash copper converting
technologies are commercially available and are being selected for new
smelters in other countries. Because these smelting technologies are
more technologically advanced and cost effective in producing copper
than the technologies currently employed at the three existing U.S.
smelters, they would likely be used in the U.S. if new smelters are
constructed.
B. What HAP are emitted from primary copper smelters?
Metals other than copper naturally occur in copper ore deposits,
and some of these metals are listed as HAP under CAA section 112(b). In
general, the HAP metals that have been found in larger quantities in
copper ore mined and smelted in the U.S. are lead and arsenic. Lesser
quantities of antimony, beryllium, cadmium, chromium, cobalt,
manganese, mercury, nickel, and selenium have also been detected. As
[[Page 59309]]
previously mentioned, the primary copper smelting area source category
was listed for regulation under CAA sections 112(c)(3) and 112(k)(3)(B)
due to emissions of the urban HAP arsenic, cadmium, chromium, nickel,
and lead.
HAP metals in the copper ore are released into the atmosphere in
the form of PM during certain high temperature operations. The
composition and quantity of the potential HAP emissions from a given
smelter are directly related to the level of metal impurities in the
copper concentrate processed at the smelter.
C. What are the proposed requirements for area sources?
1. Applicability and Compliance Dates
The proposed NESHAP applies to each new or existing primary copper
smelter that is an area source of HAP. Because the one existing area
source is already operating subject to PM control requirements that are
the same as those in this proposed NESHAP, we are proposing that an
existing affected source comply by [DATE OF PUBLICATION OF THE FINAL
RULE IN THE Federal Register]. A new affected source would be required
to comply by [DATE OF PUBLICATION OF THE FINAL RULE IN THE Federal
Register] or upon initial startup, whichever is later.
2. Emissions Limits and Work Practice Standards
The owner or operator of an existing area source would be required
to control HAP emissions from copper concentrate drying, copper
concentrate smelting, copper matte drying and grinding, copper matte
converting, and copper anode refining and casting operations. The
proposed NESHAP requires that gases and fumes generated by these
processes be captured and vented through one or more PM control
devices. Total PM emissions from the captured gas streams from all of
these processes would be limited on a smelter-wide basis to no greater
than 89.5 pounds per hour (lb/hr) as determined on a 24-hour average
basis.
Similarly, the owner or operator of a new area source would be
required to control HAP emissions from all primary copper smelting
processes, including but not limited to those processes mentioned above
that are applicable to the new sources's smelter design. The proposed
standard requires that gases and fumes generated by these processes at
a new source be captured and vented through one or more PM control
devices. However, instead of the 89.5 lb/hr emissions limit, we would
require a new source to achieve a facility input-based emission rate
for total PM no greater than a daily (24-hour) average of 0.6 pounds
per ton (lb/ton) of copper concentrate feed charged to the smelting
vessel.
The proposed NESHAP also require a secondary gas system for each
smelting vessel and converting vessel that collects the gases and fumes
released during the molten material transfer operations and conveys the
collected gas stream to a control device. Capture systems that collect
gas and fumes and convey them to a control device also would be
required for operations in the anode refining and casting department.
3. Compliance Requirements
For existing area sources, we are proposing to apply the testing,
monitoring, recordkeeping, and reporting requirements for PM emissions
currently applicable to the only existing area source smelter.
Compliance with the proposed emissions limit for existing area sources
would be based on the daily average PM emissions measured by a PM CEMS.
The owner or operator would submit reports of deviations within two
weeks of the date the deviation occurred, monthly summaries of
monitoring data, and semiannual monitoring reports. We are also
proposing that the owner or operator comply with the requirements in 40
CFR 63.6(e)(3) for SSM plans and reports.
The owner or operator of an existing area source would be required
to comply with notification requirements in 40 CFR 63.9 of the General
Provisions (40 CFR part 63, subpart A). In the notification of
compliance status required in 40 CFR 63.9(h), the owner or operator
would be allowed to certify initial compliance with the proposed
emissions limit based on monitoring data collected during the previous
month. The owner or operator would also certify initial compliance with
the work practice standards.
The owner or operator of a new primary copper smelter would be
required to install, operate, and maintain a CEMS to measure and record
PM concentrations and gas stream flow rates for each emissions source
subject to the emissions limit. The proposed NESHAP requires that the
PM CEMS meet EPA Performance Specification 11 (40 CFR part 60, appendix
B). A device to measure and record the weight of the copper concentrate
feed charged to the smelting furnace each day also would be required.
The owner or operator would be required to continuously monitor PM
emissions, determine and record the daily (24-hour) value for each day,
and calculate and record the daily average pounds of total PM per ton
of copper concentrate feed charged to the smelting furnace. A monthly
summary report of the daily averages of PM per ton of copper
concentrate feed charged to the smelting vessel also would be required.
All notification, monitoring, testing, operation and maintenance,
recordkeeping, and reporting requirements of the part 63 General
Provisions would apply to the owner or operator of a new source.
D. What is our rationale for selecting the proposed standards for area
sources?
1. Selection of Pollutants
The HAP emissions from primary copper smelters originate primarily
from metal impurities that naturally occur in copper ore concentrates.
During the smelting process and the subsequent converting process to
produce blister copper, these HAP metal species either are eliminated
in the molten slag tapped from the process vessels or are vaporized and
discharged in the off-gases vented from the vessels. HAP metals may
also be emitted from other processes that contain molten materials,
such as anode refining and the casting operation. Upon cooling of the
process off-gas, the volatilized HAP metal species condense, form
aerosols, and behave as PM.
The composition and amounts of metal HAP in the copper ore
concentrates can vary from one smelter to another, as well as over time
at individual smelters depending on the ore deposit from which the
copper ore concentrate is obtained. This inherent variability and
unpredictability of the metal HAP compositions and amounts in copper
ore concentrates have a material effect on the composition and amount
of HAP metals in the process off-gas emissions at the smelter. As a
result, establishing individual numerical emissions limits for each HAP
metal species is difficult given the level of uncertainty about the
individual metal HAP compositions of the copper ores processed at a
smelter.
An emissions characteristic common to all smelters and similar
source categories is that metal HAP are a component of the PM contained
in the process off-gas discharged from smelting, converting, anode
refining, and casting operations. Emissions limits established to
achieve control of PM will also achieve control of metal HAP other than
mercury. Consequently, we chose to use PM as a surrogate for the urban
HAP, which are metal HAP, in establishing emissions limits. This
approach is consistent with the
[[Page 59310]]
approach we used for the emissions limits established in the NESHAP for
primary copper smelters in 40 CFR part 63, subpart QQQ.
2. Selection of Proposed Standards
We are aware of only one existing primary copper smelter that is an
area source. This smelter was built in the mid-1990's and uses flash
copper converting technology. The smelter was originally designed to
use the most advanced controls that were available at that time to
achieve emissions reductions that met or exceeded levels required to
comply with the existing State and Federal requirements to control PM
emissions. Extensive emissions controls and work practices are used for
all process and fugitive PM emissions sources at this smelter to
control PM and therefore metal HAP emissions.
The existing area source smelter operates emissions control systems
that capture and control off-gases from the copper concentrate drying,
smelting, converting, and anode refining and casting operations. All
process gases from these copper smelting operations are routed to
control devices (for many sources, a series of control devices) that
achieve high-efficiency removal of PM and metal HAP from the gas stream
before being discharged through a single main stack. Also included in
the combined gas stream vented through this main stack are captured
gases and fumes from the smelting and converting furnaces' tapping
ports and launders and from the matte drying and grinding operations.
The work practices described above to control PM and metal HAP
emissions are requirements in this area source smelter's current title
V permit. The smelter's ability to demonstrate compliance with these
requirements on a long-term basis indicates that the facility owner has
the technical and economic capabilities to implement these
requirements, which are highly effective in controlling PM and metal
HAP emissions. Therefore, we conclude that these requirements reflect
GACT for primary copper area source smelters.
The source has a total PM emissions limit for the main stack gases.
This facility-wide PM emissions limit for the smelter process off-gases
is based on the operating practices and the emissions control system
configurations used at this area source smelter. The maximum allowable
PM emissions level for the smelter as measured at the main stack is
89.5 lb/hr based on a 24-hour average. A continuous sampling system
that measures PM is installed in the main stack. Results from this
continuous sampler are used to calculate the 24-hour average for each
day of the month with a summary of the 24-hour averages reported to the
State each month for the previous month.
PM and metal HAP emissions are effectively controlled at this
existing area source by its compliance with the facility-wide emissions
limit and work practice standards mentioned above, which are
requirements in its title V permit. Although these requirements in
certain aspects are specific to this facility, we think it is
appropriate to adopt these requirements as the standards for existing
sources of primary copper production because this is the only existing
area source in this source category.
We are not certain that a new smelter would use flash copper
converting technology, and if it did, that it would be in the
configuration installed at the existing smelter. A new smelter may use
one of the other commercially available continuous smelting and
converting technologies that are based on bath smelting technology or
an innovative new continu