Information Collection Request Submitted to OMB for Review and Approval; Comment Request; Ethylene Oxide Commercial Sterilization Facilities National Emission Standards for Hazardous Air Pollutants (NESHAP) Technology Review, 24862-24863 [2021-09794]
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Federal Register / Vol. 86, No. 88 / Monday, May 10, 2021 / Notices
by sources to achieve those standards.
The draft TMDL report and information
pertaining to the virtual public meeting
is available from EPA Region 3’s website
at: https://www.epa.gov/tmdl/revisedsediment-tmdl-indian-creek-watershedmontgomery-county-pennsylvania.
Comments must be received on
or before June 24, 2021. The public is
welcomed to attend a virtual public
meeting on June 8, 2021 from 1–2:30
p.m.
DATES:
Comments on the draft
TMDL must be received in writing and
sent by electronic mail to Ms. Jillian
Adair at adair.jillian@epa.gov or by mail
to Ms. Jillian Adair, Water Division
(3WD42), U.S. Environmental Protection
Agency Region 3, 1650 Arch Street,
Philadelphia, PA 19103–2029.
Electronic mail submissions including
body text and attachments are limited to
25 megabytes. In addition, EPA cannot
receive electronic mail attachments in
ZIP format (.zip). To attend the virtual
public meeting, please use the weblink
or conference line phone number
provided at the above weblink in the
SUMMARY.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Jillian Adair at adair.jillian@epa.gov or
(215) 814–5713.
On June
30, 2008, EPA established a sediment
TMDL for the Indian Creek Watershed.
On October 17, 2011 a complaint was
filed against EPA regarding the TMDL
[Civil Action No. 2:11–cv–06489–CDJ
(E.D.PA)]. EPA then agreed to
reconsider the TMDL and investigate
several concerns raised by the plaintiffs.
On March 21, 2014, EPA issued a
reconsideration document, which
identified certain concerns that the
reference watershed approach and
sediment loading rates used should be
revisited. The court granted EPA’s
request for a voluntary remand of the
2008 sediment TMDL on April 3, 2014.
EPA subsequently solicited input to
seek relevant data and feedback,
including four stakeholder meetings
from 2014 to 2018 as part of its efforts
to develop a revised draft sediment
TMDL. EPA considered the information
and data that were submitted by various
stakeholders as part of the TMDL
development effort. That information
can also be accessed at the above
weblink in the SUMMARY.
khammond on DSKJM1Z7X2PROD with NOTICES
SUPPLEMENTARY INFORMATION:
Leslie Gillespie-Marthaler,
Deputy Director, Water Division, Region III.
[FR Doc. 2021–09762 Filed 5–7–21; 8:45 am]
BILLING CODE 6560–50–P
VerDate Sep<11>2014
19:05 May 07, 2021
Jkt 253001
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OAR–2019–0178; FRL–10023–89–
OMS]
Information Collection Request
Submitted to OMB for Review and
Approval; Comment Request; Ethylene
Oxide Commercial Sterilization
Facilities National Emission Standards
for Hazardous Air Pollutants (NESHAP)
Technology Review
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
The U.S. Environmental
Protection Agency (EPA) has submitted
an information collection request (ICR),
Ethylene Oxide Commercial
Sterilization Facilities National
Emission Standards for Hazardous Air
Pollutants (NESHAP) Technology
Review (EPA ICR Number 2623.01,
OMB Control Number 2060–NEW), to
the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act (PRA). This is a request
for approval of a new collection. Public
comments were previously requested
via the Federal Register on June 12,
2020, during a 60-day comment period.
This notice allows for an additional 30
days for public comments. A complete
description of the ICR is provided
below, including its estimated burden
and cost to the public. 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.
DATES: Additional comments may be
submitted on or before June 9, 2021.
ADDRESSES: Submit your comments to
EPA, referencing Docket ID No. EPA–
HQ–OAR–2019–0178, online using
www.regulations.gov (our preferred
method), by email to a-and-r-docket@
epa.gov, or by mail to: EPA Docket
Center, Environmental Protection
Agency, Mail Code 28221T, 1200
Pennsylvania Ave. NW, Washington, DC
20460. EPA’s policy is that all
comments received will be included in
the public docket without change
including any personal information
provided, unless the comment includes
profanity, threats, information claimed
to be Confidential Business Information
(CBI), or other information whose
disclosure is restricted by statute.
Submit written comments and
recommendations to OMB for the
proposed information collection within
30 days of publication of this notice to
www.reginfo.gov/public/do/PRAMain.
SUMMARY:
PO 00000
Frm 00024
Fmt 4703
Sfmt 4703
Find this particular information
collection by selecting ‘‘Currently under
30-day Review—Open for Public
Comments’’ or by using the search
function.
FOR FURTHER INFORMATION CONTACT: Mr.
Matthew Witosky, Sector Policies and
Programs Division (E143–05), U.S.
Environmental Protection Agency,
Research Triangle Park, NC 27711;
telephone number: (919) 541–2865;
email address: witosky.matthew@
epa.gov.
SUPPLEMENTARY INFORMATION:
Supporting documents explaining in
detail the information that the EPA will
be collecting are available in the public
docket for this ICR. The docket can be
viewed online at https://
www.regulations.gov/. The telephone
number for the Docket Center is (202)
566–1742. For additional information
about EPA’s Docket Center services and
the current status, please visit us online
at https://www.epa.gov/dockets.
Abstract: The NESHAP for EtO
Commercial Sterilization and
Fumigation Operations were finalized in
December 1994 at 40 CFR part 63,
subpart O. The NESHAP establishes
emission standards for both major and
area sources that use at least 1 ton of
EtO in sterilization or fumigation
operations in any 12-month period. The
standards require existing and new
major sources to control emissions to
the level achievable by the maximum
achievable control technology and
require existing and new area sources to
control emissions using generally
available control technology. The EPA
completed a residual risk and
technology review for the NESHAP in
2006 and, at that time, concluded that
the risk under existing standards were
acceptable and provided an ample
margin of safety. More recently, in 2016,
the EPA released its updated Integrated
Risk Information System unit risk
estimate for EtO, which indicated that
cancer risks from EtO were significantly
higher than previously understood.
Subsequently, the National Air Toxics
Assessment (NATA) released in August
2018, identified EtO emissions as an
important risk driver in several areas
across the country. Further investigation
revealed the EtO Commercial
Sterilization source category contributes
to some of these risks, which has led the
EPA to evaluate, in greater depth,
potential options to reduce emissions of
EtO from the source category.
Since 2019, the EPA has been
gathering additional information to
evaluate opportunities to reduce EtO
emissions through potential rule
revisions and more immediate emission
E:\FR\FM\10MYN1.SGM
10MYN1
khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 86, No. 88 / Monday, May 10, 2021 / Notices
reduction steps. The goal of the data
gathering efforts is to better understand
the emissions sources, measurement
and monitoring techniques, and
available control technologies and their
associated efficiencies. These efforts
have included an advance notice of
proposed rulemaking (ANPRM)
requesting facility-specific data on
process controls and operational
practices as well as a CAA section 114
questionnaire that was distributed to 9
companies engaged in EtO commercial
sterilization. The instructions and
questionnaire were posted to the EPA
web page where they were accessed by
facilities. Electronic responses were
required within 60 days or by February
6, 2020. While these data gathering
efforts have been successful, there are
still several important information gaps
that should be filled prior to any final
rulemaking activity. Therefore, the EPA
is now exercising its authority under
section 114(a) of the CAA to broaden its
data collection efforts to include all
facilities subject to 40 CFR part 63,
subpart O that were not involved in the
December 2019 questionnaire. The data
collected through the initial
questionnaire and this new ICR would
enable the EPA to have a complete
understanding of all emissions,
emissions sources, processes, and
control technologies in use at EtO
sterilization facilities nationwide,
providing a robust foundation for a final
rulemaking.
Form numbers: Main Questionnaire;
Supplement 1 (as needed); Supplement
2 (as needed); Supplement 3 (as
needed).
Respondents/affected entities:
Facilities subject to 40 CFR part 63,
subpart O that are not included in the
initial December 2019 questionnaire.
Respondent’s obligation to respond:
Responses to the ICR are mandatory
under the authority of section 114 of the
CAA. All respondents are required to
fill out the main questionnaire, while
Supplements 1, 2, and 3 may be filled
out as needed.
Estimated number of respondents: 61
(total).
Frequency of response: This is a onetime questionnaire.
Total estimated burden: 6,573 hours
(per year). Burden is defined at 5 CFR
1320.03(b)
Total estimated cost: $604,027 (per
year), includes $920 annualized capital
or operation & maintenance costs.
VerDate Sep<11>2014
19:05 May 07, 2021
Jkt 253001
Changes in the estimates: This is a
new collection. Therefore, there is no
change in burden.
Courtney Kerwin,
Director, Regulatory Support Division.
[FR Doc. 2021–09794 Filed 5–7–21; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–10023–47–Region 9]
Public Water System Supervision
Program Revision for the State of
Nevada
Environmental Protection
Agency (EPA).
ACTION: Notice of tentative approval.
AGENCY:
Notice is hereby given that
the State of Nevada (State) revised its
approved Public Water System
Supervision (PWSS) Program under the
federal Safe Drinking Water Act (SDWA)
by incorporating by reference the federal
Arsenic Rule The Environmental
Protection Agency (EPA) has
determined that the State’s revisions are
no less stringent than the corresponding
Federal regulations and otherwise meet
applicable SDWA primacy
requirements. Therefore, EPA intends to
approve the stated revisions to the
State’s PWSS Program.
DATES: A request for a public hearing
must be received on or before June 9,
2021.
SUMMARY:
All documents relating to
this determination are available for
inspection online at https://ndep.nv.gov/
posts. In addition, documents relating to
this determination are available for
inspection by appointment between the
hours of 8:30 a.m. and 4:00 p.m.,
Monday through Friday, except official
State or Federal holidays at the
following address: Nevada Department
of Environmental Protection,
Administration Office, 901 South
Stewart Street, Suite 4001, Carson City,
NV 89701. Please contact the Bureau of
Safe Drinking Water at (775) 687–9521
to schedule an appointment.
FOR FURTHER INFORMATION CONTACT:
Jacob Jenzen, United States
Environmental Protection Agency,
Region 9, Drinking Water Section, via
telephone number: (415) 972–3570 or
email address: Jenzen.Jacob@epa.gov.
SUPPLEMENTARY INFORMATION:
Background. EPA approved the
State’s initial application for PWSS
Program primary enforcement authority
(‘‘primacy’’) on February 27, 1978 (43
FR 8030). Since initial approval, EPA
ADDRESSES:
PO 00000
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24863
has approved various revisions to
Nevada’s PWSS Program. For the
revisions covered by this action, EPA
revised the Arsenic Rule on January 22,
2001 (66 FR 6976). The revisions
included a more stringent federal
standard for arsenic in drinking water
from 0.050 mg/L to 0.010 mg/L to better
protect public health. The State
submitted its final application to add
the Arsenic Rule to its approved PWSS
Program on December 30, 2011,
followed by an application supplement
on February 11, 2021. EPA has
determined that the Arsenic Rule was
incorporated by reference into the
Nevada Administrative Code (NAC),
Title 40 Chapter 445A, in a manner that
Nevada’s regulations are comparable to
and no less stringent than the federal
requirements. EPA has also determined
that State’s primacy revision meets all of
the regulatory requirements for
approval, as set forth in 40 CFR 142.12,
including a side-by-side comparison of
the Federal requirements and the
corresponding State authorities,
additional materials to support special
primacy requirements of 40 CFR 142.16,
and a statement by the Nevada Attorney
General certifying that Nevada’s laws
and regulations adopted by the State to
carry out the program revisions were
duly adopted and are enforceable.
Therefore, EPA intends to approve the
State’s revisions as part of its PWSS
Program.
Public Process. Any interested party
may request a public hearing on this
determination. A request for a public
hearing must be received or postmarked
by June 9, 2021, and addressed to the
Regional Administrator at the EPA
Region 9, via the following email
address: R9dw-program@epa.gov. Please
note, ‘‘State Primacy Rule
Determination’’ in the subject line of the
email. The Regional Administrator may
deny frivolous or insubstantial requests
for a hearing. If a substantial request for
a public hearing is made by June 9,
2021, EPA Region 9 will hold a public
hearing. Any request for a public
hearing shall include the following
information: 1. The name, address, and
telephone number of the individual,
organization, or other entity requesting
a hearing; 2. A brief statement of the
requesting person’s interest in the
Regional Administrator’s determination
and a brief statement of the information
that the requesting person intends to
submit at such hearing; and 3. The
signature of the individual making the
request, or, if the request is made on
behalf of an organization or other entity,
the signature of a responsible official of
the organization or other entity.
E:\FR\FM\10MYN1.SGM
10MYN1
Agencies
[Federal Register Volume 86, Number 88 (Monday, May 10, 2021)]
[Notices]
[Pages 24862-24863]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-09794]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OAR-2019-0178; FRL-10023-89-OMS]
Information Collection Request Submitted to OMB for Review and
Approval; Comment Request; Ethylene Oxide Commercial Sterilization
Facilities National Emission Standards for Hazardous Air Pollutants
(NESHAP) Technology Review
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The U.S. Environmental Protection Agency (EPA) has submitted
an information collection request (ICR), Ethylene Oxide Commercial
Sterilization Facilities National Emission Standards for Hazardous Air
Pollutants (NESHAP) Technology Review (EPA ICR Number 2623.01, OMB
Control Number 2060-NEW), to the Office of Management and Budget (OMB)
for review and approval in accordance with the Paperwork Reduction Act
(PRA). This is a request for approval of a new collection. Public
comments were previously requested via the Federal Register on June 12,
2020, during a 60-day comment period. This notice allows for an
additional 30 days for public comments. A complete description of the
ICR is provided below, including its estimated burden and cost to the
public. 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.
DATES: Additional comments may be submitted on or before June 9, 2021.
ADDRESSES: Submit your comments to EPA, referencing Docket ID No. EPA-
HQ-OAR-2019-0178, online using www.regulations.gov (our preferred
method), by email to [email protected], or by mail to: EPA Docket
Center, Environmental Protection Agency, Mail Code 28221T, 1200
Pennsylvania Ave. NW, Washington, DC 20460. EPA's policy is that all
comments received will be included in the public docket without change
including any personal information provided, unless the comment
includes profanity, threats, information claimed to be Confidential
Business Information (CBI), or other information whose disclosure is
restricted by statute.
Submit written comments and recommendations to OMB for the proposed
information collection within 30 days of publication of this notice to
www.reginfo.gov/public/do/PRAMain. Find this particular information
collection by selecting ``Currently under 30-day Review--Open for
Public Comments'' or by using the search function.
FOR FURTHER INFORMATION CONTACT: Mr. Matthew Witosky, Sector Policies
and Programs Division (E143-05), U.S. Environmental Protection Agency,
Research Triangle Park, NC 27711; telephone number: (919) 541-2865;
email address: [email protected].
SUPPLEMENTARY INFORMATION: Supporting documents explaining in detail
the information that the EPA will be collecting are available in the
public docket for this ICR. The docket can be viewed online at https://www.regulations.gov/. The telephone number for the Docket Center is
(202) 566-1742. For additional information about EPA's Docket Center
services and the current status, please visit us online at https://www.epa.gov/dockets.
Abstract: The NESHAP for EtO Commercial Sterilization and
Fumigation Operations were finalized in December 1994 at 40 CFR part
63, subpart O. The NESHAP establishes emission standards for both major
and area sources that use at least 1 ton of EtO in sterilization or
fumigation operations in any 12-month period. The standards require
existing and new major sources to control emissions to the level
achievable by the maximum achievable control technology and require
existing and new area sources to control emissions using generally
available control technology. The EPA completed a residual risk and
technology review for the NESHAP in 2006 and, at that time, concluded
that the risk under existing standards were acceptable and provided an
ample margin of safety. More recently, in 2016, the EPA released its
updated Integrated Risk Information System unit risk estimate for EtO,
which indicated that cancer risks from EtO were significantly higher
than previously understood. Subsequently, the National Air Toxics
Assessment (NATA) released in August 2018, identified EtO emissions as
an important risk driver in several areas across the country. Further
investigation revealed the EtO Commercial Sterilization source category
contributes to some of these risks, which has led the EPA to evaluate,
in greater depth, potential options to reduce emissions of EtO from the
source category.
Since 2019, the EPA has been gathering additional information to
evaluate opportunities to reduce EtO emissions through potential rule
revisions and more immediate emission
[[Page 24863]]
reduction steps. The goal of the data gathering efforts is to better
understand the emissions sources, measurement and monitoring
techniques, and available control technologies and their associated
efficiencies. These efforts have included an advance notice of proposed
rulemaking (ANPRM) requesting facility-specific data on process
controls and operational practices as well as a CAA section 114
questionnaire that was distributed to 9 companies engaged in EtO
commercial sterilization. The instructions and questionnaire were
posted to the EPA web page where they were accessed by facilities.
Electronic responses were required within 60 days or by February 6,
2020. While these data gathering efforts have been successful, there
are still several important information gaps that should be filled
prior to any final rulemaking activity. Therefore, the EPA is now
exercising its authority under section 114(a) of the CAA to broaden its
data collection efforts to include all facilities subject to 40 CFR
part 63, subpart O that were not involved in the December 2019
questionnaire. The data collected through the initial questionnaire and
this new ICR would enable the EPA to have a complete understanding of
all emissions, emissions sources, processes, and control technologies
in use at EtO sterilization facilities nationwide, providing a robust
foundation for a final rulemaking.
Form numbers: Main Questionnaire; Supplement 1 (as needed);
Supplement 2 (as needed); Supplement 3 (as needed).
Respondents/affected entities: Facilities subject to 40 CFR part
63, subpart O that are not included in the initial December 2019
questionnaire.
Respondent's obligation to respond: Responses to the ICR are
mandatory under the authority of section 114 of the CAA. All
respondents are required to fill out the main questionnaire, while
Supplements 1, 2, and 3 may be filled out as needed.
Estimated number of respondents: 61 (total).
Frequency of response: This is a one-time questionnaire.
Total estimated burden: 6,573 hours (per year). Burden is defined
at 5 CFR 1320.03(b)
Total estimated cost: $604,027 (per year), includes $920 annualized
capital or operation & maintenance costs.
Changes in the estimates: This is a new collection. Therefore,
there is no change in burden.
Courtney Kerwin,
Director, Regulatory Support Division.
[FR Doc. 2021-09794 Filed 5-7-21; 8:45 am]
BILLING CODE 6560-50-P