Approval and Promulgation of Air Quality Implementation Plans; Illinois; Volatile Organic Compound Site-Specific State Implementation Plan for Abbott Laboratories, 40760-40762 [2010-17139]
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40760
Federal Register / Vol. 75, No. 134 / Wednesday, July 14, 2010 / Proposed Rules
NOAA is opening a public comment
period to:
1. Solicit public comments and
identify issues on the continued
management of the Hawaiian Islands
Humpback Whale National Marine
Sanctuary; and
2. Help determine the scope of issues
to be addressed in the preparation of a
management plan and an environmental
impact statement (EIS) pursuant to the
National Environmental Policy Act
(NEPA), if warranted; and
3. Conduct a series of statewide
scoping meetings across the State of
Hawai’i to collect public comment. The
intent of the scoping meetings is to
gather information and other comments
from individuals, organizations, and
government agencies on the scope,
types, and significance of issues related
to the sanctuary’s management plan and
regulations. These scoping meetings
will also help determine the scope of
issues to be addressed in the
preparation of an EIS pursuant to the
NEPA, 43 U.S.C. 4321 et seq., if
warranted. The public scoping meeting
schedule is presented below.
This notice confirms that NOAA will
coordinate its responsibilities under
section 106 of the National Historic
Preservation Act (NHPA, 16 U.S.C. 470)
with its ongoing NEPA process,
pursuant to 36 CFR 800.8(a)—
coordination with NEPA—including the
use of NEPA documents and public and
stakeholder meetings to also meet the
section 106 requirements. The NHPA
specifically applies to any agency
undertaking that has an adverse effect
on historic properties. Pursuant to 36
CFR 800.16(1)(1), historic properties
includes: ‘‘any prehistoric or historic
district, site, building, structure or
object included in, or eligible for
inclusion in, the National Register of
Historic Places maintained by the
Secretary of the Interior. The term
includes artifacts, records, and remains
that are related to and located within
such properties. The term includes
properties of traditional religious and
cultural importance to an Indian tribe or
Native Hawaiian organization and that
meet the National Register criteria.’’
In coordinating its responsibilities
under the NHPA and NEPA, NOAA
intends to identify consulting parties;
identify historic properties and assess
the effects of the undertaking on such
properties; initiate formal consultation
with the Hawaii State Historic
Preservation Officer, the Advisory
Council of Historic Preservation, and
other consulting parties; involve the
public in accordance with NOAA’s
NEPA procedures, and develop in
consultation with identified consulting
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parties alternatives and proposed
measures that might avoid, minimize or
mitigate any adverse effects on historic
properties and describe them in any
Environmental Assessment or Draft
Environmental Impact Statement.
Public Scoping Meetings: The public
scoping meetings will be held on the
following dates and at the following
locations beginning at 6 p.m. unless
otherwise noted:
1. Hilo, Hawai’I, Tuesday, August 10,
¯
Mokupapapa Discovery Center, 308
Kamehameha Avenue, Suite 109,
Hilo, HI 96720.
2. Kailua-Kona, Hawai’I, Wednesday,
August 11, Outrigger Keauhou Beach
Resort, 78–6740 Ali’i Drive, KailuaKona, HI 96740.
3. Honolulu, O’ahu, Thursday, August
12, 5:30 p.m. to 8:30 p.m., Central
Union Church, 1660 South Beretania
Street, Honolulu, HI 96826.
¯
4. Lıhu’e, Kaua’I, Saturday, August 14,
9 a.m. to 12 p.m., Chiefess
Kamakahelei Middle School Cafeteria,
¯
4431 Nuhou Street, Lıhu’e, HI 96766.
5. Kilauea, Kaua’I, Saturday, August 14,
4 p.m. to 7 p.m., Kaua’i Christian
Academy Library, 4000 Kilauea Road,
Kilauea, HI 96754.
¯
6. Kıhei, Maui, Monday, August 16,
Lokilani Middle School, 1401 Liloa
¯
Drive, Kıhei, HI 96753.
7. Lahaina, Maui, Tuesday, August 17,
Lahaina Civic Center, 1840
Honoapi’ilani Highway, Lahaina, HI
96761.
8. Kaunakakai, Moloka’I, Wednesday,
August 18, Mitchell Pauole Center, 90
Ainoa Street, Kaunakakai, HI 96748.
9. Hale’iwa, O’ahu, Monday, August 23,
Sunset Beach Elementary School, 59–
360 Kamehameha Highway, Hale’iwa,
HI 96712.
10. Lana’i City, Lana’I, Wednesday,
August 26, Lana’i High and
Elementary School, 555 Fraser
Avenue, Lana’i City, HI 96763.
Condition Report
In preparation for management plan
review, NOAA has produced a
Hawaiian Islands Humpback Whale
National Marine Sanctuary 2010
Condition Report. The Condition Report
provides a summary of resources, with
a specific focus on humpback whales in
the sanctuary, pressures on those
resources, the current condition and
trends, and management responses to
the pressures that threaten the integrity
of the marine environment. Specifically,
the Condition Report includes
information on the status and trends of
water quality, habitat, living resources
and maritime archaeological resources
and the human activities that affect
them. The report serves as a supporting
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document for the Management Plan
Review Process, to inform constituents
of the current status of humpback
whales in the sanctuary.
An electronic copy of the final
Hawaiian Islands Humpback Whale
National Marine Sanctuary 2010
Condition Report is available to the
public on the Internet at: https://
sanctuaries.noaa.gov/science/condition/
welcome.html or it can be accessed from
the HIHWNMS Web site at: https://
hawaiihumpbackwhale.noaa.gov/.
Scoping Comments
Scoping meetings provide an
opportunity to make direct comments to
NOAA on the management of the
sanctuary’s natural and cultural
resources, including administrative
programs. We encourage the public to
participate and welcome any comments
related to the sanctuary. In particular,
we are interested in hearing about the
public’s view on the sanctuary’s
potential management priorities for the
next ten to fifteen years. Specifically,
the sanctuary is seeking input on a
proposal to expand its scope and
direction to protect and conserve other
living marine resources, in addition to
humpback whales and submerged
cultural heritage resources within the
sanctuary. This proposal is detailed in
the State of the Sanctuary Report
Special Management Plan Review
Edition and is available to the public on
the Internet at: https://
hawaiihumpbackwhale.noaa.gov/
management/management_plan
_review.html.
Authority: 16 U.S.C. 1431 et seq; 16 U.S.C.
470.
(Federal Domestic Assistance Catalog
Number 11.429 Marine Sanctuary Program)
Dated: July 7, 2010.
Daniel J. Basta,
Director for the Office of National Marine
Sanctuaries.
[FR Doc. 2010–17083 Filed 7–13–10; 8:45 am]
BILLING CODE 3510–NK–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 52
[EPA–R05–OAR–2009–0665; FRL–9175–3]
Approval and Promulgation of Air
Quality Implementation Plans; Illinois;
Volatile Organic Compound SiteSpecific State Implementation Plan for
Abbott Laboratories
AGENCY: Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
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Federal Register / Vol. 75, No. 134 / Wednesday, July 14, 2010 / Proposed Rules
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SUMMARY: EPA is proposing to approve
Illinois’ amendments to its
manufacturing rules into the Illinois
State Implementation Plan (SIP). On
July 17, 2009, the Illinois Environmental
Protection Agency (Illinois EPA)
submitted amendments to its
pharmaceutical manufacturing rules for
approval into its SIP. These
amendments consist of a site-specific
rulemaking for certain of Abbott
Laboratories’ (Abbott) tunnel dryers and
fluid bed dryers. This site-specific rule
revision is approvable because it lowers
the allowable emissions from these
dryers and it is consistent with the
Clean Air Act (CAA) and EPA
regulations.
DATES: Comments must be received on
or before August 13, 2010.
ADDRESSES: Submit your comments,
identified by Docket ID No. EPA–R05–
OAR–2009–0665, by one of the
following methods:
1. https://www.regulations.gov: Follow
the on-line instructions for submitting
comments.
2. E-mail: bortzer.jay@epa.gov.
3. Fax: (312) 692–2054.
4. Mail: Jay Bortzer, Chief, Air
Programs Branch (AR–18J), U.S.
Environmental Protection Agency, 77
West Jackson Boulevard, Chicago,
Illinois 60604.
5. Hand Delivery: Jay Bortzer, Chief,
Air Programs Branch (AR–18J), U.S.
Environmental Protection Agency, 77
West Jackson Boulevard, Chicago,
Illinois 60604. Such deliveries are only
accepted during the regional office
normal hours of operation, and special
arrangements should be made for
deliveries of boxed information. The
Regional Office official hours of
business are Monday through Friday,
8:30 a.m. to 4:30 p.m., excluding
Federal holidays.
Instructions: Direct your comments to
Docket ID No. EPA–R05–OAR–2009–
0665. EPA’s policy is that all comments
received will be included in the public
docket without change and may be
made available online at https://
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through https://
www.regulations.gov or e-mail. The
https://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.
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If you send an e-mail comment directly
to EPA without going through https://
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 and any form of
encryption, and be free of any defects or
viruses. For additional instructions on
submitting comments, go to Section I of
the SUPPLEMENTARY INFORMATION section
of this document.
Docket: All documents in the docket
are listed in the https://
www.regulations.gov index. Although
listed in the index, some information is
not publicly available, e.g., CBI or other
information whose disclosure is
restricted by statute. Certain other
material, such as copyrighted material,
will be publicly available only in hard
copy. Publicly available docket
materials are available either
electronically in https://
www.regulations.gov or in hard copy at
the Environmental Protection Agency,
Region 5, Air and Radiation Division, 77
West Jackson Boulevard, Chicago,
Illinois 60604. This facility is open from
8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding Federal holidays. We
recommend that you telephone Steven
Rosenthal at (312) 886–6052 before
visiting the Region 5 office.
FOR FURTHER INFORMATION CONTACT:
Steven Rosenthal, Environmental
Engineer, Attainment Planning and
Maintenance Section, Air Programs
Branch (AR–18J), Environmental
Protection Agency, Region 5, 77 West
Jackson Boulevard, Chicago, Illinois
60604, (312) 886–6052.
SUPPLEMENTARY INFORMATION:
Throughout this document whenever
‘‘we,’’ ‘‘us,’’ or ‘‘our’’ is used, we mean
EPA. This supplementary information
section is arranged as follows:
I. What should I consider as I prepare my
comments for EPA?
II. What action is EPA proposing to take?
III. What is the background for this action?
IV. What is EPA’s analysis of Illinois’ revised
pharmaceutical manufacturing rule?
V. Statutory and Executive Order Reviews
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40761
I. What should I consider as I prepare
my comments for EPA?
When submitting comments,
remember to:
1. Identify the rulemaking by docket
number and other identifying
information (subject heading, Federal
Register date, and page number).
2. Follow directions—EPA may ask
you to respond to specific questions or
organize comments by referencing a
Code of Federal Regulations (CFR) part
or section number.
3. Explain why you agree or disagree;
suggest alternatives and substitute
language for your requested changes.
4. Describe any assumptions and
provide any technical information and/
or data that you used.
5. If you estimate potential costs or
burdens, explain how you arrived at
your estimate in sufficient detail to
allow for it to be reproduced.
6. Provide specific examples to
illustrate your concerns, and suggest
alternatives.
7. Explain your views as clearly as
possible, avoiding the use of profanity
or personal threats.
8. Make sure to submit your
comments by the comment period
deadline identified.
II. What action is EPA proposing to
take?
EPA is proposing to approve revisions
to Illinois’ pharmaceutical
manufacturing rule for three of Abbott’s
fluid bed dryers and four of its tunnel
dryers. Each of the three fluid bed
dryers previously had a five tons
volatile organic compound (VOC) per
year applicability cutoff and each of the
four tunnel dryers had a 7.5 tons VOC
per year applicability cutoff. This rule
revision replaces these individual
cutoffs with an overall combined cutoff
for all seven dryers of 20.6 tons VOC per
year.
III. What is the background for this
action?
This rule revision was requested by
Abbott to provide it with more
manufacturing flexibility. Abbott owns a
pharmaceutical manufacturing facility
located in Lake County, Illinois.
Abbott’s operations are subject to the
emission standards for VOCs at 35 Ill.
Adm. Code, Subpart T—Pharmaceutical
Manufacturing (Subpart T rules).
Section 218.480(b) contains certain
exemptions that are only applicable to
Abbott’s air suspension coater/dryer,
fluid bed dryers, tunnel dryers, and
Accelacotas. This rule revision amends
these site-specific exemptions by
capping and lowering the overall
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emissions allowable under the
exemptions from its tunnel dryers
numbered #1, #2, #3, and #4, and fluid
bed dryers numbered #1, #2, and #3.
This amendment reduces combined
cutoffs for these seven dryers while
increasing Abbott’s operational
flexibility, by allowing it to make
preferential use of the more efficient
fluid bed dryers.
IV. What is EPA’s analysis of Illinois’
revised pharmaceutical manufacturing
rule?
The revisions to Illinois’
pharmaceutical manufacturing rule are
approvable because it lowers the total
allowable emissions from seven dryers
and is consistent with the CAA, EPA
regulations, and relevant policy.
More specifically, the individual
applicability cutoffs for the seven
affected dryers results in a combined
allowable emission total of 45 tons of
VOC per year. The 45 tons VOC per year
is based on a 5 tons VOC cutoff (in prior
subsection 218.480(b)(2)) for each of the
three fluid bed dryers and a 7.5 tons
VOC per year cutoff (in prior subsection
218.480 (b)(3) for each of the four tunnel
dryers. This compares with a 20.6 tons
VOC per year total in new subsection
218.480(b)(4) for tunnel dryers
numbered #1, #2, #3, and #4, and fluid
bed dryers numbered #1, #2, and #3.
Subsection 218.480(b)(4) replaces
subsections 218.480(b)(2) and
218.480(b)(3) for these seven dryers.
The main basis for evaluating this
proposal is EPA’s January 2001 policy
on Economic Incentive Programs (EIP),
which is EPA’s applicable policy for
evaluating emission averaging plans,
also referred to as ‘‘bubbles.’’ Under the
EIP policy, a combined emission limit is
based on the lower of actual or
allowable emissions. Actual emissions
are based on the highest consecutive
two-year period during the preceding
ten-year period, which in this case is
1999–2000. The average annual actual
emissions for the seven dryers during
this two-year period was calculated to
be 22.9 tons VOC per year. The EIP
policy also requires reducing this
annual emission average by ten percent
to establish an environmental benefit.
This results in a combined emission
limit of 20.6 tons VOC per year, which
is the value in the new subsection
218.480(b)(4).
Illinois amended its July 17, 2009, SIP
submittal in a May 12, 2010, letter and
attachments from Laurel L. Kroack,
Chief, Bureau of Air, Illinois
Environmental Protection Agency, to
EPA. This letter establishes how
compliance with Abbott’s 20.6 tons
VOC per year limit is determined as
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well as Abbott’s recordkeeping
requirements. Specifically, this letter
states:
It is the Illinois EPA’s interpretation that
compliance with Abbott’s 20.6 tons VOC per
year limit shall be determined on a monthly
basis from the sum of the data for the current
month plus the preceding 11 months
(running 12 month total) consistent with
Condition 7.1.6(i) of Abbott’s current Title V
permit #96010010, issued on September 26,
2007. Compliance will be demonstrated
according to the compliance calculation
methodology and corresponding
recordkeeping procedures in Katherine
Hodge’s April 23, 2008 email to EPA,
including both the body of the email and its
attachments, as well as the compliance
procedures in Condition 7.1.12(e) of Abbott’s
current Title V permit. Also, Abbott’s
recordkeeping requirements should also be
consistent with the recordkeeping
requirements reflected in Katherine Hodge’s
April 23, 2008 email, including both the
body of the e-mail and its attachments. These
records would need to be maintained for five
years.
V. Statutory and Executive Order
Reviews
Under the CAA, the Administrator is
required to approve a SIP submission
that complies with the provisions of the
CAA and applicable Federal regulations.
42 U.S.C. 7410(k); 40 CFR 52.02(a).
Thus, in reviewing SIP submissions,
EPA’s role is to approve state choices,
provided that they meet the criteria of
the CAA. Accordingly, this action
merely approves state law as meeting
Federal requirements and does not
impose additional requirements beyond
those imposed by state law. For that
reason, this action:
• Is not a ‘‘significant regulatory
action’’ subject to review by the Office
of Management and Budget under
Executive Order 12866 (58 FR 51735,
October 4, 1993);
• Does not impose an information
collection burden under the provisions
of the Paperwork Reduction Act (44
U.S.C. 3501 et seq.);
• Is certified as not having a
significant economic impact on a
substantial number of small entities
under the Regulatory Flexibility Act
(5 U.S.C. 601 et seq.);
• Does not contain any unfunded
mandate or significantly or uniquely
affect small governments, as described
in the Unfunded Mandates Reform Act
of 1995 (Pub. L. 104–4);
• Does not have Federalism
implications as specified in Executive
Order 13132 (64 FR 43255, August 10,
1999);
• Is not an economically significant
regulatory action based on health or
safety risks subject to Executive Order
13045 (62 FR 19885, April 23, 1997);
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• Is not a significant regulatory action
subject to Executive Order 13211 (66 FR
28355, May 22, 2001);
• Is not subject to requirements of
Section 12(d) of the National
Technology Transfer and Advancement
Act of 1995 (15 U.S.C. 272 note) because
application of those requirements would
be inconsistent with the CAA; and
• Does not provide EPA with the
discretionary authority to address, as
appropriate, disproportionate human
health or environmental effects, using
practicable and legally permissible
methods, under Executive Order 12898
(59 FR 7629, February 16, 1994).
In addition, this rule does not have
tribal implications as specified by
Executive Order 13175 (65 FR 67249,
November 9, 2000), because the SIP is
not approved to apply in Indian country
located in the state, and EPA notes that
it will not impose substantial direct
costs on tribal governments or preempt
tribal law.
List of Subjects in 40 CFR Part 52
Environmental protection, Air
pollution control, Intergovernmental
relations, Nitrogen dioxide, Ozone,
Reporting and recordkeeping
requirements, Volatile organic
compounds.
Dated: June 30, 2010.
Walter W. Kovalick Jr.,
Acting Regional Administrator, Region 5.
[FR Doc. 2010–17139 Filed 7–13–10; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 52
[EPA–R09–OAR–2010–0514; FRL–9172–2]
Revisions to the California State
Implementation Plan, Sacramento
Metropolitan Air Quality Management
District and South Coast Air Quality
Management District
AGENCY: Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
SUMMARY: EPA is proposing to approve
revisions to the Sacramento
Metropolitan Air Quality Management
District (SMAQMD) and South Coast Air
Quality Management District
(SCAQMD) portions of the California
State Implementation Plan (SIP). These
revisions concern volatile organic
compound (VOC) emissions from
vanishing oils, rust inhibitors, plastic
coatings, rubber coatings, glass coatings,
and aerospace operations. We are
proposing to approve these local rules to
E:\FR\FM\14JYP1.SGM
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Agencies
[Federal Register Volume 75, Number 134 (Wednesday, July 14, 2010)]
[Proposed Rules]
[Pages 40760-40762]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-17139]
=======================================================================
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 52
[EPA-R05-OAR-2009-0665; FRL-9175-3]
Approval and Promulgation of Air Quality Implementation Plans;
Illinois; Volatile Organic Compound Site-Specific State Implementation
Plan for Abbott Laboratories
AGENCY: Environmental Protection Agency (EPA).
ACTION: Proposed rule.
-----------------------------------------------------------------------
[[Page 40761]]
SUMMARY: EPA is proposing to approve Illinois' amendments to its
manufacturing rules into the Illinois State Implementation Plan (SIP).
On July 17, 2009, the Illinois Environmental Protection Agency
(Illinois EPA) submitted amendments to its pharmaceutical manufacturing
rules for approval into its SIP. These amendments consist of a site-
specific rulemaking for certain of Abbott Laboratories' (Abbott) tunnel
dryers and fluid bed dryers. This site-specific rule revision is
approvable because it lowers the allowable emissions from these dryers
and it is consistent with the Clean Air Act (CAA) and EPA regulations.
DATES: Comments must be received on or before August 13, 2010.
ADDRESSES: Submit your comments, identified by Docket ID No. EPA-R05-
OAR-2009-0665, by one of the following methods:
1. https://www.regulations.gov: Follow the on-line instructions for
submitting comments.
2. E-mail: bortzer.jay@epa.gov.
3. Fax: (312) 692-2054.
4. Mail: Jay Bortzer, Chief, Air Programs Branch (AR-18J), U.S.
Environmental Protection Agency, 77 West Jackson Boulevard, Chicago,
Illinois 60604.
5. Hand Delivery: Jay Bortzer, Chief, Air Programs Branch (AR-18J),
U.S. Environmental Protection Agency, 77 West Jackson Boulevard,
Chicago, Illinois 60604. Such deliveries are only accepted during the
regional office normal hours of operation, and special arrangements
should be made for deliveries of boxed information. The Regional Office
official hours of business are Monday through Friday, 8:30 a.m. to 4:30
p.m., excluding Federal holidays.
Instructions: Direct your comments to Docket ID No. EPA-R05-OAR-
2009-0665. EPA's policy is that all comments received will be included
in the public docket without change and may be made available online at
https://www.regulations.gov, including any personal information
provided, unless the comment includes information claimed to be
Confidential Business Information (CBI) or other information whose
disclosure is restricted by statute. Do not submit information that you
consider to be CBI or otherwise protected through https://www.regulations.gov or e-mail. The https://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 https://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 and any form of encryption, and be free
of any defects or viruses. For additional instructions on submitting
comments, go to Section I of the SUPPLEMENTARY INFORMATION section of
this document.
Docket: All documents in the docket are listed in the https://www.regulations.gov index. Although listed in the index, some
information is not publicly available, e.g., CBI or other information
whose disclosure is restricted by statute. Certain other material, such
as copyrighted material, will be publicly available only in hard copy.
Publicly available docket materials are available either electronically
in https://www.regulations.gov or in hard copy at the Environmental
Protection Agency, Region 5, Air and Radiation Division, 77 West
Jackson Boulevard, Chicago, Illinois 60604. This facility is open from
8:30 a.m. to 4:30 p.m., Monday through Friday, excluding Federal
holidays. We recommend that you telephone Steven Rosenthal at (312)
886-6052 before visiting the Region 5 office.
FOR FURTHER INFORMATION CONTACT: Steven Rosenthal, Environmental
Engineer, Attainment Planning and Maintenance Section, Air Programs
Branch (AR-18J), Environmental Protection Agency, Region 5, 77 West
Jackson Boulevard, Chicago, Illinois 60604, (312) 886-6052.
SUPPLEMENTARY INFORMATION: Throughout this document whenever ``we,''
``us,'' or ``our'' is used, we mean EPA. This supplementary information
section is arranged as follows:
I. What should I consider as I prepare my comments for EPA?
II. What action is EPA proposing to take?
III. What is the background for this action?
IV. What is EPA's analysis of Illinois' revised pharmaceutical
manufacturing rule?
V. Statutory and Executive Order Reviews
I. What should I consider as I prepare my comments for EPA?
When submitting comments, remember to:
1. Identify the rulemaking by docket number and other identifying
information (subject heading, Federal Register date, and page number).
2. Follow directions--EPA may ask you to respond to specific
questions or organize comments by referencing a Code of Federal
Regulations (CFR) part or section number.
3. Explain why you agree or disagree; suggest alternatives and
substitute language for your requested changes.
4. Describe any assumptions and provide any technical information
and/or data that you used.
5. If you estimate potential costs or burdens, explain how you
arrived at your estimate in sufficient detail to allow for it to be
reproduced.
6. Provide specific examples to illustrate your concerns, and
suggest alternatives.
7. Explain your views as clearly as possible, avoiding the use of
profanity or personal threats.
8. Make sure to submit your comments by the comment period deadline
identified.
II. What action is EPA proposing to take?
EPA is proposing to approve revisions to Illinois' pharmaceutical
manufacturing rule for three of Abbott's fluid bed dryers and four of
its tunnel dryers. Each of the three fluid bed dryers previously had a
five tons volatile organic compound (VOC) per year applicability cutoff
and each of the four tunnel dryers had a 7.5 tons VOC per year
applicability cutoff. This rule revision replaces these individual
cutoffs with an overall combined cutoff for all seven dryers of 20.6
tons VOC per year.
III. What is the background for this action?
This rule revision was requested by Abbott to provide it with more
manufacturing flexibility. Abbott owns a pharmaceutical manufacturing
facility located in Lake County, Illinois. Abbott's operations are
subject to the emission standards for VOCs at 35 Ill. Adm. Code,
Subpart T--Pharmaceutical Manufacturing (Subpart T rules). Section
218.480(b) contains certain exemptions that are only applicable to
Abbott's air suspension coater/dryer, fluid bed dryers, tunnel dryers,
and Accelacotas. This rule revision amends these site-specific
exemptions by capping and lowering the overall
[[Page 40762]]
emissions allowable under the exemptions from its tunnel dryers
numbered 1, 2, 3, and 4, and fluid
bed dryers numbered 1, 2, and 3. This
amendment reduces combined cutoffs for these seven dryers while
increasing Abbott's operational flexibility, by allowing it to make
preferential use of the more efficient fluid bed dryers.
IV. What is EPA's analysis of Illinois' revised pharmaceutical
manufacturing rule?
The revisions to Illinois' pharmaceutical manufacturing rule are
approvable because it lowers the total allowable emissions from seven
dryers and is consistent with the CAA, EPA regulations, and relevant
policy.
More specifically, the individual applicability cutoffs for the
seven affected dryers results in a combined allowable emission total of
45 tons of VOC per year. The 45 tons VOC per year is based on a 5 tons
VOC cutoff (in prior subsection 218.480(b)(2)) for each of the three
fluid bed dryers and a 7.5 tons VOC per year cutoff (in prior
subsection 218.480 (b)(3) for each of the four tunnel dryers. This
compares with a 20.6 tons VOC per year total in new subsection
218.480(b)(4) for tunnel dryers numbered 1, 2,
3, and 4, and fluid bed dryers numbered 1,
2, and 3. Subsection 218.480(b)(4) replaces
subsections 218.480(b)(2) and 218.480(b)(3) for these seven dryers.
The main basis for evaluating this proposal is EPA's January 2001
policy on Economic Incentive Programs (EIP), which is EPA's applicable
policy for evaluating emission averaging plans, also referred to as
``bubbles.'' Under the EIP policy, a combined emission limit is based
on the lower of actual or allowable emissions. Actual emissions are
based on the highest consecutive two-year period during the preceding
ten-year period, which in this case is 1999-2000. The average annual
actual emissions for the seven dryers during this two-year period was
calculated to be 22.9 tons VOC per year. The EIP policy also requires
reducing this annual emission average by ten percent to establish an
environmental benefit. This results in a combined emission limit of
20.6 tons VOC per year, which is the value in the new subsection
218.480(b)(4).
Illinois amended its July 17, 2009, SIP submittal in a May 12,
2010, letter and attachments from Laurel L. Kroack, Chief, Bureau of
Air, Illinois Environmental Protection Agency, to EPA. This letter
establishes how compliance with Abbott's 20.6 tons VOC per year limit
is determined as well as Abbott's recordkeeping requirements.
Specifically, this letter states:
It is the Illinois EPA's interpretation that compliance with
Abbott's 20.6 tons VOC per year limit shall be determined on a
monthly basis from the sum of the data for the current month plus
the preceding 11 months (running 12 month total) consistent with
Condition 7.1.6(i) of Abbott's current Title V permit
96010010, issued on September 26, 2007. Compliance will be
demonstrated according to the compliance calculation methodology and
corresponding recordkeeping procedures in Katherine Hodge's April
23, 2008 email to EPA, including both the body of the email and its
attachments, as well as the compliance procedures in Condition
7.1.12(e) of Abbott's current Title V permit. Also, Abbott's
recordkeeping requirements should also be consistent with the
recordkeeping requirements reflected in Katherine Hodge's April 23,
2008 email, including both the body of the e-mail and its
attachments. These records would need to be maintained for five
years.
V. Statutory and Executive Order Reviews
Under the CAA, the Administrator is required to approve a SIP
submission that complies with the provisions of the CAA and applicable
Federal regulations. 42 U.S.C. 7410(k); 40 CFR 52.02(a). Thus, in
reviewing SIP submissions, EPA's role is to approve state choices,
provided that they meet the criteria of the CAA. Accordingly, this
action merely approves state law as meeting Federal requirements and
does not impose additional requirements beyond those imposed by state
law. For that reason, this action:
Is not a ``significant regulatory action'' subject to
review by the Office of Management and Budget under Executive Order
12866 (58 FR 51735, October 4, 1993);
Does not impose an information collection burden under the
provisions of the Paperwork Reduction Act (44 U.S.C. 3501 et seq.);
Is certified as not having a significant economic impact
on a substantial number of small entities under the Regulatory
Flexibility Act (5 U.S.C. 601 et seq.);
Does not contain any unfunded mandate or significantly or
uniquely affect small governments, as described in the Unfunded
Mandates Reform Act of 1995 (Pub. L. 104-4);
Does not have Federalism implications as specified in
Executive Order 13132 (64 FR 43255, August 10, 1999);
Is not an economically significant regulatory action based
on health or safety risks subject to Executive Order 13045 (62 FR
19885, April 23, 1997);
Is not a significant regulatory action subject to
Executive Order 13211 (66 FR 28355, May 22, 2001);
Is not subject to requirements of Section 12(d) of the
National Technology Transfer and Advancement Act of 1995 (15 U.S.C. 272
note) because application of those requirements would be inconsistent
with the CAA; and
Does not provide EPA with the discretionary authority to
address, as appropriate, disproportionate human health or environmental
effects, using practicable and legally permissible methods, under
Executive Order 12898 (59 FR 7629, February 16, 1994).
In addition, this rule does not have tribal implications as
specified by Executive Order 13175 (65 FR 67249, November 9, 2000),
because the SIP is not approved to apply in Indian country located in
the state, and EPA notes that it will not impose substantial direct
costs on tribal governments or preempt tribal law.
List of Subjects in 40 CFR Part 52
Environmental protection, Air pollution control, Intergovernmental
relations, Nitrogen dioxide, Ozone, Reporting and recordkeeping
requirements, Volatile organic compounds.
Dated: June 30, 2010.
Walter W. Kovalick Jr.,
Acting Regional Administrator, Region 5.
[FR Doc. 2010-17139 Filed 7-13-10; 8:45 am]
BILLING CODE 6560-50-P