Information Collection Request Submitted to OMB for Review and Approval; Comment Request; Underground Injection Control Program (Renewal), 11068-11069 [2022-04106]
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11068
Federal Register / Vol. 87, No. 39 / Monday, February 28, 2022 / Notices
Changes in the Estimates: There is an
adjustment decrease in the total
estimated burden as currently identified
in the OMB Inventory of Approved
Burdens. This decrease is not due to any
program changes. The adjustment
decrease in burden from the most
recently-approved ICR is due to a
decrease in the number of sources.
Consultations with the Agency’s
internal industry experts have shown
that a number of cell chlor-alkali plants
have shut down since the previous ICR
renewal, leading to a decrease in
respondent labor hours and the number
of responses. There are no capital or
operation and maintenance costs
associated with this ICR. The overall
result is a decrease in burden.
Courtney Kerwin,
Director, Regulatory Support Division.
[FR Doc. 2022–04133 Filed 2–25–22; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OW–2014–0359; FRL–9615–01–
OMS]
Information Collection Request
Submitted to OMB for Review and
Approval; Comment Request;
Underground Injection Control
Program (Renewal)
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
The Environmental Protection
Agency has submitted an information
collection request (ICR), Underground
Injection Control (UIC) Program (EPA
ICR Number 0370.27, OMB Control
Number 2040–0042) to the Office of
Management and Budget (OMB) for
review and approval in accordance with
the Paperwork Reduction Act (PRA).
This is a proposed extension of the ICR,
which is currently approved through
April 30, 2022. Public comments were
previously requested via the Federal
Register on August 25, 2021, during a
60-day comment period. This notice
allows for an additional 30 days for
public comments. A fuller description
of the ICR is given 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 March 30, 2022.
ADDRESSES: Submit your comments,
referencing Docket ID Number EPA–
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:23 Feb 25, 2022
Jkt 256001
HQ–OW–2014–0359, to EPA online
using https://www.regulations.gov (our
preferred method), by email to OWDocket@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 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: Kyle
Carey, Drinking Water Protection
Division, Office of Ground Water and
Drinking Water, 4606M, Environmental
Protection Agency, 1200 Pennsylvania
Ave. NW, Washington, DC 20460;
telephone number: (202) 564–2322; fax
number: (202) 564–3756; email address:
carey.kyle@epa.gov.
SUPPLEMENTARY INFORMATION:
Supporting documents, which explain
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 or in person at the
EPA Docket Center, WJC West, Room
3334, 1301 Constitution Ave. NW,
Washington, DC 20004. The telephone
number for the Docket Center is 202–
566–1744. For additional information
about EPA’s public docket, visit https://
www.epa.gov/dockets.
Abstract: EPA developed the
Underground Injection Control (UIC)
Program under the authority of the Safe
Drinking Water Act to establish a
federal-state regulatory system to protect
underground sources of drinking water
(USDWs) from injection fluids and
injection-related activities. These rules
are designed to ensure that Americans
receive safe drinking water, and ensure
fair treatment and meaningful
involvement of all people regardless of
race, color, national origin, or income.
Injected fluids include hazardous waste,
oil field brines or produced water,
mineral processing fluids, various types
of industrial fluids, automotive,
sanitary, and other wastes, and carbon
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
dioxide injected for geologic
sequestration. Owners or operators of
injection wells must obtain permits,
conduct environmental monitoring,
maintain records, and report results to
EPA or the state agency (if the state has
UIC primary enforcement responsibility
(primacy)). States must report to EPA on
permittee compliance and related
information. This mandatory
information is reported using
standardized forms and annual reports.
Reporting data are used by UIC
authorities to ensure the protection of
USDWs.
Form Numbers: 7520–1, 7520–2A,
7520–2B, 7520–3, 7520–4, 7520–6,
7520–7, 7520–8, 7520–11, 7520–16,
7520–17, 7520–18, and 7520–19.
Respondents/affected entities:
Owners or operators of underground
injection wells and State UIC primacy
agencies.
Respondent’s obligation to respond:
Mandatory (40 CFR parts 144 through
148).
Estimated number of respondents:
37,677 (total).
Frequency of response: Annual, semiannual, quarterly.
Total estimated burden: 1,631,360
hours (per year). Burden is defined at 5
CFR 1320.03(b).
Total estimated cost: $363,309,464
(per year), includes $276,069,465
annualized capital or operation and
maintenance costs.
Changes in the estimates: There is an
increase of 339,100 hours in the total
estimated respondent burden compared
with the ICR currently approved by
OMB. This increase is due to
adjustments that include an increase in
the number of Class I, Class II, Class III,
and Class VI permit applications
expected to be prepared and reviewed
by UIC permitting authorities during the
upcoming ICR period. The overall
increase is partially offset by an
inventory adjustment that results in a
decrease in the number of current
operators that will perform monitoring,
reporting, and recordkeeping activities
over the life of an injection project (due
to decreases in the injection well
inventory). Programmatic changes that
result in minor changes to the burden
estimate include revisions to the
reporting forms and changes in
reporting of primacy state program
information, including implementing
electronic reporting options (which will
reduce the burden to primacy agencies)
and anticipated approval of Class VI
UIC Program primacy for several states,
which will increase state burden (by
E:\FR\FM\28FEN1.SGM
28FEN1
Federal Register / Vol. 87, No. 39 / Monday, February 28, 2022 / Notices
shifting burden from EPA to the
approved states).
Courtney Kerwin,
Director, Regulatory Support Division.
[FR Doc. 2022–04106 Filed 2–25–22; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–HQ–OPPT–2022–0132; FRL–9411–01–
OCSPP]
Certain New Chemicals; Receipt and
Status Information for January 2022
Environmental Protection
Agency (EPA).
ACTION: Notice.
AGENCY:
EPA is required under the
Toxic Substances Control Act (TSCA) to
make certain information publicly
available and to publish information in
the Federal Register pertaining to
submissions, including notice of receipt
of a Premanufacture notice (PMN),
Significant New Use Notice (SNUN) or
Microbial Commercial Activity Notice
(MCAN), including an amended notice
or test information; an exemption
application (Biotech exemption); an
application for a test marketing
exemption (TME), both pending and/or
concluded; a notice of commencement
(NOC) of manufacture (including
import) for new chemical substances;
and a periodic status report on new
chemical substances that are currently
under EPA review or have recently
concluded review. This document
covers the period from 01/01/2022 to
01/31/2022.
DATES: Comments identified by the
specific case number provided in this
document must be received on or before
March 30, 2022.
ADDRESSES: Submit your comments,
identified by docket identification (ID)
number EPA–HQ–OPPT–2022–0132,
and the specific case number for the
chemical substance related to your
comment, through the Federal
eRulemaking Portal at https://
www.regulations.gov. Follow the online
instructions for submitting comments.
Do not submit electronically any
information you consider to be
Confidential Business Information (CBI)
or other information whose disclosure is
restricted by statute. Additional
instructions on commenting or visiting
the docket, along with more information
about dockets generally, is available at
https://www.epa.gov/dockets.
Due to the public health concerns
related to COVID–19, the EPA Docket
Center (EPA/DC) and Reading Room is
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:23 Feb 25, 2022
Jkt 256001
closed to visitors with limited
exceptions. The staff continues to
provide remote customer service via
email, phone, and webform. For the
latest status information on EPA/DC
services and docket access, visit https://
www.epa.gov/dockets.
FOR FURTHER INFORMATION CONTACT:
For technical information contact: Jim
Rahai, Project Management and
Operations Division (7407M), Office of
Pollution Prevention and Toxics,
Environmental Protection Agency, 1200
Pennsylvania Ave. NW, Washington, DC
20460–0001; telephone number: (202)
564–8593; email address: rahai.jim@
epa.gov.
For general information contact: The
TSCA-Hotline, ABVI-Goodwill, 422
South Clinton Ave., Rochester, NY
14620; telephone number: (202) 554–
1404; email address: TSCA-Hotline@
epa.gov.
SUPPLEMENTARY INFORMATION:
I. Executive Summary
A. What action is the Agency taking?
This document provides the receipt
and status reports for the period from
01/01/2022 to 01/31/2022. The Agency
is providing notice of receipt of PMNs,
SNUNs, and MCANs (including
amended notices and test information);
an exemption application under 40 CFR
part 725 (Biotech exemption); TMEs,
both pending and/or concluded; NOCs
to manufacture a new chemical
substance; and a periodic status report
on new chemical substances that are
currently under EPA review or have
recently concluded review.
EPA is also providing information on
its website about cases reviewed under
the amended TSCA, including the
section 5 PMN/SNUN/MCAN and
exemption notices received, the date of
receipt, the final EPA determination on
the notice, and the effective date of
EPA’s determination for PMN/SNUN/
MCAN notices on its website at: https://
www.epa.gov/reviewing-new-chemicalsunder-toxic-substances-control-act-tsca/
status-pre-manufacture-notices. This
information is updated on a weekly
basis.
B. What is the Agency’s authority for
taking this action?
Under TSCA, 15 U.S.C. 2601 et seq.,
a chemical substance may be either an
‘‘existing’’ chemical substance or a
‘‘new’’ chemical substance. Any
chemical substance that is not on EPA’s
TSCA Inventory of Chemical Substances
(TSCA Inventory) is classified as a ‘‘new
chemical substance,’’ while a chemical
substance that is listed on the TSCA
Inventory is classified as an ‘‘existing
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
11069
chemical substance.’’ (See TSCA section
3(11).) For more information about the
TSCA Inventory please go to: https://
www.epa.gov/tsca-inventory.
Any person who intends to
manufacture (including import) a new
chemical substance for a non-exempt
commercial purpose, or to manufacture
or process a chemical substance in a
non-exempt manner for a use that EPA
has determined is a significant new use,
is required by TSCA section 5 to
provide EPA with a PMN, MCAN, or
SNUN, as appropriate, before initiating
the activity. EPA will review the notice,
make a risk determination on the
chemical substance or significant new
use, and take appropriate action as
described in TSCA section 5(a)(3).
TSCA section 5(h)(1) authorizes EPA
to allow persons, upon application and
under appropriate restrictions, to
manufacture or process a new chemical
substance, or a chemical substance
subject to a significant new use rule
(SNUR) issued under TSCA section
5(a)(2), for ‘‘test marketing’’ purposes,
upon a showing that the manufacture,
processing, distribution in commerce,
use, and disposal of the chemical will
not present an unreasonable risk of
injury to health or the environment.
This is referred to as a test marketing
exemption, or TME. For more
information about the requirements
applicable to a new chemical go to:
https://www.epa.gov/oppt/newchems.
Under TSCA sections 5 and 8 and
EPA regulations, EPA is required to
publish in the Federal Register certain
information, including notice of receipt
of a PMN/SNUN/MCAN (including
amended notices and test information);
an exemption application under 40 CFR
part 725 (biotech exemption); an
application for a TME, both pending
and concluded; NOCs to manufacture a
new chemical substance; and a periodic
status report on the new chemical
substances that are currently under EPA
review or have recently concluded
review.
C. Does this action apply to me?
This action provides information that
is directed to the public in general.
D. Does this action have any
incremental economic impacts or
paperwork burdens?
No.
E. What should I consider as I prepare
my comments for EPA?
1. Submitting confidential business
information (CBI). Do not submit this
information to EPA through
regulations.gov or email. Clearly mark
the part or all of the information that
E:\FR\FM\28FEN1.SGM
28FEN1
Agencies
[Federal Register Volume 87, Number 39 (Monday, February 28, 2022)]
[Notices]
[Pages 11068-11069]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-04106]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[EPA-HQ-OW-2014-0359; FRL-9615-01-OMS]
Information Collection Request Submitted to OMB for Review and
Approval; Comment Request; Underground Injection Control Program
(Renewal)
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Environmental Protection Agency has submitted an
information collection request (ICR), Underground Injection Control
(UIC) Program (EPA ICR Number 0370.27, OMB Control Number 2040-0042) to
the Office of Management and Budget (OMB) for review and approval in
accordance with the Paperwork Reduction Act (PRA). This is a proposed
extension of the ICR, which is currently approved through April 30,
2022. Public comments were previously requested via the Federal
Register on August 25, 2021, during a 60-day comment period. This
notice allows for an additional 30 days for public comments. A fuller
description of the ICR is given 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 March 30,
2022.
ADDRESSES: Submit your comments, referencing Docket ID Number EPA-HQ-
OW-2014-0359, to EPA online using https://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 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: Kyle Carey, Drinking Water Protection
Division, Office of Ground Water and Drinking Water, 4606M,
Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington,
DC 20460; telephone number: (202) 564-2322; fax number: (202) 564-3756;
email address: [email protected].
SUPPLEMENTARY INFORMATION: Supporting documents, which explain 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 or in person at the EPA Docket Center, WJC
West, Room 3334, 1301 Constitution Ave. NW, Washington, DC 20004. The
telephone number for the Docket Center is 202-566-1744. For additional
information about EPA's public docket, visit https://www.epa.gov/dockets.
Abstract: EPA developed the Underground Injection Control (UIC)
Program under the authority of the Safe Drinking Water Act to establish
a federal-state regulatory system to protect underground sources of
drinking water (USDWs) from injection fluids and injection-related
activities. These rules are designed to ensure that Americans receive
safe drinking water, and ensure fair treatment and meaningful
involvement of all people regardless of race, color, national origin,
or income. Injected fluids include hazardous waste, oil field brines or
produced water, mineral processing fluids, various types of industrial
fluids, automotive, sanitary, and other wastes, and carbon dioxide
injected for geologic sequestration. Owners or operators of injection
wells must obtain permits, conduct environmental monitoring, maintain
records, and report results to EPA or the state agency (if the state
has UIC primary enforcement responsibility (primacy)). States must
report to EPA on permittee compliance and related information. This
mandatory information is reported using standardized forms and annual
reports. Reporting data are used by UIC authorities to ensure the
protection of USDWs.
Form Numbers: 7520-1, 7520-2A, 7520-2B, 7520-3, 7520-4, 7520-6,
7520-7, 7520-8, 7520-11, 7520-16, 7520-17, 7520-18, and 7520-19.
Respondents/affected entities: Owners or operators of underground
injection wells and State UIC primacy agencies.
Respondent's obligation to respond: Mandatory (40 CFR parts 144
through 148).
Estimated number of respondents: 37,677 (total).
Frequency of response: Annual, semi-annual, quarterly.
Total estimated burden: 1,631,360 hours (per year). Burden is
defined at 5 CFR 1320.03(b).
Total estimated cost: $363,309,464 (per year), includes
$276,069,465 annualized capital or operation and maintenance costs.
Changes in the estimates: There is an increase of 339,100 hours in
the total estimated respondent burden compared with the ICR currently
approved by OMB. This increase is due to adjustments that include an
increase in the number of Class I, Class II, Class III, and Class VI
permit applications expected to be prepared and reviewed by UIC
permitting authorities during the upcoming ICR period. The overall
increase is partially offset by an inventory adjustment that results in
a decrease in the number of current operators that will perform
monitoring, reporting, and recordkeeping activities over the life of an
injection project (due to decreases in the injection well inventory).
Programmatic changes that result in minor changes to the burden
estimate include revisions to the reporting forms and changes in
reporting of primacy state program information, including implementing
electronic reporting options (which will reduce the burden to primacy
agencies) and anticipated approval of Class VI UIC Program primacy for
several states, which will increase state burden (by
[[Page 11069]]
shifting burden from EPA to the approved states).
Courtney Kerwin,
Director, Regulatory Support Division.
[FR Doc. 2022-04106 Filed 2-25-22; 8:45 am]
BILLING CODE 6560-50-P