Spring 2024 Unified Agenda of Regulatory and Deregulatory Actions, 66866-66875 [2024-16459]
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ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Ch. I
[FRL 11974–01–OA; EPA–HQ–OAR–2011–
0135; EPA–HQ–OAR–2024–0089]
Spring 2024 Unified Agenda of
Regulatory and Deregulatory Actions
Environmental Protection
Agency.
ACTION: Semiannual Regulatory Agenda.
AGENCY:
The Environmental Protection
Agency (EPA) publishes the Semiannual
Agenda of Regulatory and Deregulatory
Actions online at https://
www.reginfo.gov to periodically update
the public. This document contains
information about:
• Regulations in the Semiannual
Agenda that are under development,
completed, or canceled since the last
agenda; and
• Reviews of regulations with small
business impacts under section 610 of
the Regulatory Flexibility Act (RFA).
FOR FURTHER INFORMATION CONTACT: If
you have questions or comments about
a particular action, please get in touch
with the agency contact listed in each
agenda entry. If you have general
questions about the Semiannual
Agenda, please contact: Caryn
Muellerleile (muellerleile.caryn@
epa.gov; 202–564–2855).
SUMMARY:
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Table of Contents
I. Introduction
A. The EPA’s Regulatory Information
B. What key statutes and Executive Orders
guide the EPA’s rule and policymaking
process?
C. How can you be involved in the EPA’s
rule and policymaking process?
II. Semiannual Agenda of Regulatory and
Deregulatory Actions
A. What actions are included in the eAgenda and the Regulatory Flexibility
Agenda?
B. How is the e-Agenda organized?
C. What information is in the Regulatory
Flexibility Agenda and the e-Agenda?
D. What tools are available for mining
Regulatory Agenda Data and for finding
more about EPA rules and policies?
III. Review of Regulations Under Section 610
of the Regulatory Flexibility Act
A. Reviews of Rules With Significant
Impacts on a Substantial Number of
Small Entities
B. What other special attention does EPA
give to the impacts of rules on small
businesses, small governments, and
small nonprofit organizations?
IV. Thank You for Collaborating With Us
SUPPLEMENTARY INFORMATION:
I. Introduction
The EPA is committed to a regulatory
strategy that effectively achieves the
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Agency’s mission of protecting human
health and the environment. The EPA
publishes the Semiannual Agenda of
Regulatory and Deregulatory Actions to
update the public about regulatory
activity undertaken in support of this
mission. In the Semiannual Agenda, the
EPA provides notice of our plans to
review, propose, and issue regulations.
The EPA is committed to environmental
protection that benefits all communities
and encourages public participation and
meaningful engagement in our
regulatory activities and processes.
Additionally, the EPA’s Semiannual
Agenda includes information about
rules that may have a significant
economic impact on a substantial
number of small entities, and review of
those regulations under the Regulatory
Flexibility Act as amended.
In this document, the EPA explains in
greater detail the types of actions and
information available in the Semiannual
Agenda and actions that are currently
undergoing review specifically for
impacts on small entities.
A. The EPA’s Regulatory Information
‘‘E-Agenda,’’ ‘‘online regulatory
agenda,’’ and ‘‘semiannual regulatory
agenda’’ all refer to the same
comprehensive collection of
information that, until 2007, was
published in the Federal Register (FR).
Currently, this information is only
available through an online database at
https://www.reginfo.gov/.
‘‘Regulatory Flexibility Agenda’’
refers to a document that contains
information about the subset of
regulations that may have a significant
impact on a substantial number of small
entities. We continue to publish this
document in the Federal Register
pursuant to the Regulatory Flexibility
Act of 1980. This document is available
at https://www.govinfo.gov/app/
collection/fr.
‘‘Unified Regulatory Agenda’’ refers to
the collection of all agencies’ agendas
with an introduction prepared by the
Regulatory Information Service Center
facilitated by the U.S. General Services
Administration.
‘‘Regulatory Agenda Preamble’’ refers
to the document you are reading now.
It appears as part of the Regulatory
Flexibility Agenda and introduces both
the EPA’s Regulatory Flexibility Agenda
and the e-Agenda.
‘‘Section 610 Review’’ as required by
the Regulatory Flexibility Act means a
periodic review within ten years of
promulgating a final rule that has or
may have a significant economic impact
on a substantial number of small
entities. The EPA maintains a list of
these actions at https://www.epa.gov/
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reg-flex/regulatory-flexibility-actsection-610-reviews. EPA is initiating
one section 610 review and is
completing another with this
semiannual agenda in spring 2024, as
described in section III.A. below.
B. What key statutes and Executive
Orders guide the EPA’s rule and
policymaking process?
Several environmental laws authorize
the EPA’s actions, including but not
limited to:
• American Innovation and
Manufacturing Act (AIM),
• Clean Air Act (CAA),
• Clean Water Act (CWA),
• Comprehensive Environmental
Response, Compensation, and
Liability Act (CERCLA, or Superfund),
• Emergency Planning and Community
Right-to-Know Act (EPCRA),
• Federal Insecticide, Fungicide, and
Rodenticide Act (FIFRA),
• Resource Conservation and Recovery
Act (RCRA),
• Safe Drinking Water Act (SDWA), and
• Toxic Substances Control Act (TSCA).
The EPA must comply not only with
environmental and other statutes, but
also with applicable administrative legal
requirements that apply to the issuance
of regulations, such as the
Administrative Procedure Act (APA),
the RFA as amended by the Small
Business Regulatory Enforcement
Fairness Act (SBREFA), the Unfunded
Mandates Reform Act (UMRA), the
Paperwork Reduction Act (PRA), the
National Technology Transfer and
Advancement Act (NTTAA), and the
Congressional Review Act (CRA).
The EPA also meets a number of
requirements contained in numerous
Executive Orders: 12866, ‘‘Regulatory
Planning and Review’’ (58 FR 51735,
Oct. 4, 1993), as supplemented by
Executive Order 13563, ‘‘Improving
Regulation and Regulatory Review’’ (76
FR 3821, Jan. 21, 2011) and amended by
Executive Order 14094, ‘‘Modernizing
Regulatory Review’’ (88 FR 21879, April
11, 2023); 12898, ‘‘Environmental
Justice’’ (59 FR 7629, Feb. 16, 1994) and
14096, ‘‘Revitalizing Our Nation’s
Commitment to Environmental Justice
for All’’ (88 FR 25251, April 26, 2023);
13045, ‘‘Children’s Health Protection’’
(62 FR 19885, Apr. 23, 1997); 13132,
‘‘Federalism’’ (64 FR 43255, Aug. 10,
1999); 13175, ‘‘Consultation and
Coordination with Indian Tribal
Governments’’ (65 FR 67249, Nov. 9,
2000); and 13211, ‘‘Actions Concerning
Regulations That Significantly Affect
Energy Supply, Distribution, or Use’’ (66
FR 28355, May 22, 2001).
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C. How can you be involved in the EPA’s
rule and policymaking process?
You can make your voice heard by
getting in touch with the contact person
provided in each agenda entry. The EPA
encourages you to participate as early in
the process as possible. You may also
participate by commenting on proposed
rules published in the Federal Register.
Instructions on how to submit your
comments through https://
www.regulations.gov are provided in
each Notice of Proposed Rulemaking
(NPRM). To be most effective,
comments should contain information
and data that support your position, and
you also should explain why the EPA
should incorporate your suggestion in
the rule or other type of action. You can
be particularly helpful and persuasive if
you provide examples to illustrate your
concerns and offer specific alternative(s)
to what has been proposed by the EPA.
The EPA believes its actions will be
more cost effective and protective if the
development process includes
stakeholders working with us to help
identify the most practical and effective
solutions to environmental problems.
The EPA encourages you to become
involved in its rule- and policymaking
processes. For more information about
the EPA’s efforts to increase
transparency, participation, and
collaboration in EPA activities, please
visit https://www.epa.gov/lawsregulations/get-involved-eparegulations.
II. Semiannual Agenda of Regulatory
and Deregulatory Actions
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A. What actions are included in the eAgenda and the Regulatory Flexibility
Agenda?
The EPA includes key regulatory
actions in the e-Agenda. However, there
is no legal significance to the omission
of an item from the agenda, and the EPA
generally does not include the following
categories of actions:
• Administrative actions such as
delegations of authority, changes of
address, or phone numbers.
• Under the CAA: Revisions to state
implementation plans; equivalent
methods for ambient air quality
monitoring; deletions from the new
source performance standards source
categories list; delegations of authority
to states; area designations for air
quality planning purposes.
• Under FIFRA: Registration-related
decisions, actions affecting the status of
currently registered pesticides, and data
call-ins.
• Under the Federal Food, Drug, and
Cosmetic Act: Actions regarding
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pesticide tolerances and food additive
regulations.
• Under TSCA: Licensing actions and
new chemical actions.
• Under RCRA: Authorization of State
solid waste management plans and
hazardous waste delisting petitions.
• Under the CWA: State Water
Quality Standards, deletions from the
section 307(a) list of toxic pollutants,
suspensions of toxic testing
requirements under the National
Pollutant Discharge Elimination System
(NPDES), and delegations of NPDES
authority to States.
• Under SDWA: Actions on State
underground injection control
programs.
Meanwhile, the Regulatory Flexibility
Agenda includes:
• Actions likely to have a significant
economic impact on a substantial
number of small entities.
• Rules the Agency has identified for
review under section 610 of the RFA.
The EPA is initiating one review and
completing another under section 610 of
the RFA in this Agenda. See section
III.A. for further detail.
B. How is the e-Agenda organized?
You can choose how to sort the
agenda entries online by specifying the
characteristics of the entries of interest
in the desired individual data fields of
the e-Agenda at https://
www.reginfo.gov. You can sort based on
the following characteristics: EPA
subagency (such as Office of Water),
stage of rulemaking as described in the
following paragraphs, alphabetically by
title, or the Regulation Identifier
Number (RIN), which is assigned
sequentially when an action is added to
the agenda.
Each entry in the agenda is associated
with one of five rulemaking stages. The
rulemaking stages are:
1. Pre-rule Stage—The EPA’s pre-rule
actions are generally intended to
determine whether the agency should
initiate rulemaking. Pre-rulemakings
may include anything that influences or
leads to rulemaking; this would include
Advance Notices of Proposed
Rulemaking (ANPRMs) or analyses of
the possible need for regulatory action.
2. Proposed Rule Stage—Proposed
rulemaking actions include the EPA’s
Notice of Proposed Rulemakings
(NPRMs); these proposals are scheduled
to publish in the Federal Register
within the next year.
3. Final Rule Stage—Final rulemaking
actions are those actions that the EPA is
scheduled to finalize and publish in the
Federal Register within the next year.
4. Long-Term Actions—This section
includes rulemakings for which the next
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scheduled regulatory action (such as
publication of a NPRM or final rule) is
twelve or more months into the future.
We encourage you to explore becoming
involved even if an action is listed in
the Long-Term category.
5. Completed Actions—The EPA’s
completed actions are those that have
been promulgated and published in the
Federal Register since publication of
the fall 2023 Agenda. This category also
includes actions that EPA is no longer
considering and has elected to
‘‘withdraw’’ and the results of any RFA
section 610 reviews.
C. What information is in the Regulatory
Flexibility Agenda and the e-Agenda?
The Regulatory Flexibility Agenda
entries include only the nine categories
of information that are required by the
Regulatory Flexibility Act of 1980 and
by Federal Register Agenda printing
requirements: Sequence Number, RIN,
Title, Description, Statutory Authority,
Section 610 Review, if applicable,
Regulatory Flexibility Analysis
Required, Schedule and Contact Person.
Note that the electronic version of the
Agenda (E-Agenda) replicates each of
these actions with more extensive
information, described below.
E-Agenda entries include:
Title: A brief description of the
subject of the regulation. The notation
’’Section 610 Review’’ follows the title
if we are reviewing the rule as part of
our periodic review of existing rules
under section 610 of the RFA (5 U.S.C.
610).
Priority: Each entry is placed into one
of the following five categories:
a. Significant under 3(f)(1): Under
Executive Order 12866, as amended, a
rulemaking that may have an annual
effect on the economy of $200 million
or more, or adversely affect in a material
way the economy, a sector of the
economy, productivity, competition,
jobs, the environment, public health or
safety, or State, local, territorial, or tribal
governments or communities.
b. Other Significant: A rulemaking
that is not economically significant but
is considered significant for other
reasons. This category includes rules
that may:
1. Create a serious inconsistency or
otherwise interfere with an action taken
or planned by another agency.
2. Materially alter the budgetary
impact of entitlements, grants, user fees,
or loan programs, or the rights and
obligations of recipients; or
3. Raise legal or policy issues for
which centralized review would
meaningfully further the President’s
priorities, or the principles in Executive
Order 12866.
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c. Substantive, Nonsignificant: A
rulemaking that has substantive impacts
but is not Significant, Routine and
Frequent, or Informational/
Administrative/Other.
d. Routine and Frequent: A
rulemaking that is a specific case of a
recurring application of a regulatory
program in the Code of Federal
Regulations. If an action that would
normally be classified Routine and
Frequent is reviewed by the Office of
Management and Budget (OMB) under
Executive Order 12866, then we would
classify the action as either ’’ Significant
under 3(f)(1)’’ or ‘‘Other Significant.’’
e. Informational/Administrative/
Other: An action that is primarily
informational or pertains to an action
outside the scope of Executive Order
12866.
Major: A rule is ‘‘major’’ under 5
U.S.C. 801 (Pub. L. 104–121) if it has
resulted or is likely to result in an
annual effect on the economy of $100
million or more or meets other criteria
specified in the Congressional Review
Act.
Unfunded Mandates: Whether the
rule is covered by section 202 of the
Unfunded Mandates Reform Act of 1995
(Pub. L. 104–4). The Act requires that,
before issuing a NPRM likely to result
in a mandate that may result in
expenditures by State, local, and tribal
governments, in the aggregate, or by the
private sector of more than $100 million
in 1 year, the agency prepare a written
statement on federal mandates
addressing costs, benefits, and
intergovernmental consultation.
Legal Authority: The sections of the
United States Code (U.S.C.), Public Law
(Pub. L.), Executive Order (E.O.), or
common name of the law that
authorizes the regulatory action.
CFR Citation: The section(s) of the
Code of Federal Regulations that would
be affected by the action.
Legal Deadline: An indication of
whether the rule is subject to a statutory
and/or a judicial deadline, the date of
that deadline, and whether the deadline
pertains to a NPRM, a Final Action, or
some other action.
Abstract: A brief description of the
problem the action will address.
Timetable: The dates and citations (if
available) for all past steps and a
projected date for at least the next step
for the regulatory action. A date
displayed in the form 03/00/2025 means
the agency is predicting the month and
year the action will take place but not
the day it will occur. For some entries,
the timetable indicates that the date of
the next action is ‘‘to be determined.’’
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Regulatory Flexibility Analysis
Required: Indicates whether the EPA
has prepared or anticipates preparing a
regulatory flexibility analysis under
section 603 or 604 of the RFA.
Generally, such an analysis is required
for proposed or final rules subject to the
RFA that the EPA believes may have a
significant economic impact on a
substantial number of small entities.
Small Entities Affected: Indicates
whether the rule is anticipated to have
any effect on small businesses, small
governments, or small nonprofit
organizations.
Government Levels Affected: Indicates
whether the rule may have any effect on
levels of government and, if so, whether
the affected governments are federal,
tribal, state, or local.
Federalism Implications: Indicates
whether the action is expected to 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.
Energy Impacts: Indicates whether the
action is a significant energy action
under Executive Order 13211.
Sectors Affected: Indicates the main
economic sectors regulated by the
action. The regulated parties are
identified by their North American
Industry Classification System (NAICS)
codes. These codes were created by the
Census Bureau for collecting, analyzing,
and publishing statistical data on the
U.S. economy. There are more than
1,000 NAICS codes for sectors in
agriculture, mining, manufacturing,
services, and public administration.
International Trade Impacts: Indicates
whether the action is likely to have
international trade or investment effects,
or otherwise be of international interest.
Agency Contact: The name, address,
phone number, and email address of a
person who is knowledgeable about the
regulation.
Additional Information: Other
information about the action including
docket information.
URLs: For some actions, the internet
addresses are included for reading
copies of rulemaking documents,
submitting comments on proposals, and
getting more information about the
rulemaking and the program of which it
is a part.
RIN: The Regulation Identifier
Number is used by the OMB and the
public to identify and track
rulemakings. The first four digits of the
RIN correspond to the EPA office with
lead responsibility for developing the
action.
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D. What tools are available for mining
Regulatory Agenda Data and for finding
more about EPA rules and policies?
1. Federal Regulatory Dashboard
The https://www.reginfo.gov
searchable database maintained by the
Regulatory Information Service Center
and the OMB’s Office of Information
and Regulatory Affairs (OIRA), allows
users to view the Regulatory Agenda
database (https://www.reginfo.gov/
public/do/eAgendaMain), with options
for searching, displaying, and
transmitting data.
2. Subject Matter EPA Websites
Some actions listed in the Agenda
include a URL for an EPA-maintained
website that provides additional
information about the action.
3. Public Dockets
When the EPA publishes either an
ANPRM or a NPRM in the Federal
Register, the Agency typically
establishes a docket to accumulate
materials developed throughout the
development process for that
rulemaking. The docket serves as the
repository for the collection of
documents or information related to that
Agency’s action or activity, and is
accessible both electronically or at the
EPA’s Docket Center Reading Room
(https://www.epa.gov/dockets). The EPA
uses dockets primarily for rulemaking
actions, but dockets may also be used
for section 610 reviews and for various
non-rulemaking activities, such as
Federal Register documents seeking
public comments on draft guidance,
policy statements, information
collection requests under the PRA, and
other non-rule activities. Docket
information should be in that action’s
agenda entry. All the EPA’s public
dockets can be located at https://
www.regulations.gov. The EPA
particularly welcomes feedback on
rulemakings from communities likely to
be affected by these actions.
III. Review of Regulations Under
Section 610 of the Regulatory
Flexibility Act
A. Reviews of Rules With Significant
Impacts on a Substantial Number of
Small Entities
Section 610 of the RFA requires that
an agency review each rule that has or
will have a significant economic impact
on a substantial number of small entities
within 10 years of promulgation. EPA is
initiating one section 610 review and
completing another.
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Review title
RIN
Docket ID No.
Section 610 Review of Standards of Performance for New Residential Wood Heaters, New Residential Hydronic Heaters and Forced-Air Furnaces.
Section 610 Review of the Tier 3 Motor Vehicle Emission and Fuel Standards ..........
2060–AW17
EPA–HQ–OAR–2024–0089
Initiated.
2060–AV90
EPA–HQ–OAR–2011–0135
Completed.
B. What other special attention does the
EPA give to the impacts of rules on
small businesses, small governments,
and small nonprofit organizations?
For each of the EPA’s rulemakings,
consideration is given to whether there
will be any adverse impact on any small
entity. The EPA attempts to fit the
regulatory requirements, to the extent
feasible, to the scale of the businesses,
organizations, and governmental
jurisdictions subject to the regulation.
Under the RFA as amended by
SBREFA, the Agency must prepare a
formal analysis of the potential negative
impacts on small entities, convene a
Small Business Advocacy Review Panel
(proposed rule stage), and prepare a
Small Entity Compliance Guide (final
rule stage) unless the Agency certifies a
rule will not have a significant
economic impact on a substantial
number of small entities. For more
detailed and current information about
the Agency’s policy and practice with
respect to implementing the RFA/
SBREFA, including ongoing Small
Business Advocacy Review Panels,
please visit the EPA’s RFA/SBREFA
website at https://www.epa.gov/reg-flex.
IV. Thank You for Collaborating With
Us
We would like to thank those of you
who choose to join with us in making
Status
progress on the complex issues involved
in protecting human health and the
environment through engaging in our
rulemaking process. Collaborative
efforts such as the EPA’s open
rulemaking processes are valuable tools
for implementing our legal requirements
to address environmental and public
health challenges. Our regulatory
agenda and your engagement play an
important role in that process.
Victoria Arroyo,
Associate Administrator, Office of Policy.
10—CLEAN AIR ACT—PRERULE STAGE
Regulation
Identifier No.
Sequence No.
Title
198 ....................
610 Review of Standards of Performance for New Residential Wood Heaters, New Residential Hydronic
Heaters and Forced-Air Furnaces (Section 610 Review).
2060–AW17
10—CLEAN AIR ACT—FINAL RULE STAGE
Regulation
Identifier No.
Sequence No.
Title
199 ....................
200 ....................
Revisions to the Air Emission Reporting Requirements (AERR) ....................................................................
National Emission Standards for Hazardous Air Pollutants: Lime Manufacturing Plants; Amendments ........
2060–AV41
2060–AV59
10—CLEAN AIR ACT—COMPLETED ACTIONS
Regulation
Identifier No.
Sequence No.
Title
201 ....................
National Emission Standards for Hazardous Air Pollutants: Ethylene Oxide Emissions Standards for Sterilization Facilities Residual Risk and Technology Review.
NSPS for GHG Emissions from New, Modified, and Reconstructed Fossil Fuel-Fired EGUs; Emission
Guidelines for GHG Emissions from Existing Fossil Fuel-Fired EGUs; and Repeal of the ACE Rule.
Standards of Performance for New, Reconstructed, and Modified Sources and Emissions Guidelines for
Existing Sources: Oil and Natural Gas Sector Climate Review.
Section 610 Review of Control of Air Pollution From Motor Vehicles: Tier 3 Motor Vehicle Emission and
Fuel Standards (Completion of a Section 610 Review).
202 ....................
203 ....................
204 ....................
2060–AU37
2060–AV09
2060–AV16
2060–AV90
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35—TSCA—PROPOSED RULE STAGE
Regulation
Identifier No.
Sequence No.
Title
205 ....................
206 ....................
207 ....................
1-Bromopropane (1–BP); Regulation Under the Toxic Substances Control Act (TSCA) ...............................
N-Methylpyrrolidone (NMP); Regulation Under the Toxic Substances Control Act (TSCA) ...........................
C.I. Pigment Violet 29; Regulation Under the Toxic Substances Control Act (TSCA) ...................................
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2070–AK85
2070–AK87
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35—TSCA—FINAL RULE STAGE
Regulation
Identifier No.
Sequence No.
Title
208 ....................
209 ....................
Trichloroethylene (TCE); Regulation Under the Toxic Substances Control Act (TSCA) ................................
Perchloroethylene (PCE); Regulation Under the Toxic Substances Control Act (TSCA) ...............................
2070–AK83
2070–AK84
35—TSCA—COMPLETED ACTIONS
Regulation
Identifier No.
Sequence No.
Title
210 ....................
Methylene Chloride; Regulation Under the Toxic Substances Control Act (TSCA) .......................................
2070–AK70
72—SDWA—COMPLETED ACTIONS
Title
211 ....................
PFAS National Primary Drinking Water Regulation Rulemaking ....................................................................
ENVIRONMENTAL PROTECTION
AGENCY (EPA)
10—Clean Air Act
Prerule Stage
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Regulation
Identifier No.
Sequence No.
198. • 610 Review of Standards of
Performance for New Residential Wood
Heaters, New Residential Hydronic
Heaters and Forced-Air Furnaces
(Section 610 Review) [2060–AW17]
Legal Authority: 42 U.S.C. 7411
Abstract: On March 16, 2015, EPA
published a final rule that made
revisions to the New Source
Performance Standards (NSPS) for new
residential wood heaters (80 FR 13672).
The 2015 final rule (40 CFR part 60,
subpart AAA and QQQQ) updated the
1988 NSPS to reflect significant
advancements in wood heater
technologies and design, broadened the
range of residential wood-heating
appliances covered by the regulation,
and improved and streamlined
implementation procedures. The 2015
rule requires manufacturers to redesign
wood heaters to be cleaner and lower
emitting. In general, the design changes
also make the heaters perform better and
more efficiently. This new entry in the
regulatory agenda announces that EPA
will review the March 16, 2015 action
pursuant to section 610 of the
Regulatory Flexibility Act (5 U.S.C. 610)
to determine if the provisions that could
affect small entities should be
maintained or should be rescinded or
amended to minimize adverse economic
impacts on small entities. As part of this
review, EPA will consider and solicit
comments on the following: (1) The
continued need for the rule; (2) the
nature of complaints or comments
received concerning the rule; (3) the
complexity of the rule; (4) the extent to
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which the rule overlaps, duplicates, or
conflicts with other Federal, State, or
local government rules; and (5) the
degree to which the technology,
economic conditions or other factors
have changed in the area affected by the
rule. Comments must be received within
60 days of this notice. In submitting
comments, please reference Docket ID
EPA–HQ–OAR–2024–0089 and follow
the instructions provided in the
preamble to this issue of the Regulatory
Agenda. This docket can be accessed at
www.regulations.gov.
Timetable:
Action
Date
Final Rule ............
Begin Review ......
End Review .........
03/16/15
07/00/24
11/00/24
FR Cite
80 FR 13672
Regulatory Flexibility Analysis
Required: No.
Agency Contact: Bill Schrock,
Environmental Protection Agency,
Office of Air and Radiation, 109 T.W.
Alexander Drive, Mail Code E143–03,
Research Triangle Park, NC 27711,
Phone: 919 541–5032, Email:
schrock.bill@epa.gov.
Nicholas Swanson, Environmental
Protection Agency, Office of Air and
Radiation, E143–03, Research Triangle
Park, NC 27711, Phone: 919 541–4080,
Email: swanson.nicholas@epa.gov.
RIN: 2060–AW17
PO 00000
2040–AG18
ENVIRONMENTAL PROTECTION
AGENCY (EPA)
10—Clean Air Act
Final Rule Stage
199. Revisions to the Air Emission
Reporting Requirements (AERR) [2060–
AV41]
Legal Authority: 42 U.S.C. 7401 et seq.
Clean Air Act
Abstract: This action finalizes
changes to the Environmental Protection
Agency’s (EPA) emissions inventory
reporting requirements to collect data
needed for the EPA to implement
pollution reduction programs and
address environmental justice concerns.
The amendments in this action would
ensure that the EPA has sufficient
information to identify and solve air
quality and exposure problems. The
amendments would also allow the EPA
to have information readily available
that the Agency needs to protect public
health and perform other activities
under the Clean Air Act (CAA or ‘‘the
Act’’). Further, the amendments would
ensure that communities have the data
needed to understand significant
sources of air pollution that may be
impacting them—including potent
carcinogens and other highly toxic
chemicals linked with a wide range of
chronic and acute health problems.
Timetable:
Action
NPRM ..................
Notice ..................
Final Rule ............
Date
08/09/23
10/12/23
07/00/24
FR Cite
88 FR 54118
88 FR 63046
Regulatory Flexibility Analysis
Required: Yes.
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Agency Contact: Marc Houyoux,
Environmental Protection Agency,
Office of Air and Radiation, C339–02,
Research Triangle Park, NC 27711,
Phone: 919 541–3649, Fax: 919 541–
0684, Email: houyoux.marc@epa.gov.
RIN: 2060–AV41
Action
NPRM ..................
Supplemental
NPRM.
Final Rule ............
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200. National Emission Standards for
Hazardous Air Pollutants: Lime
Manufacturing Plants; Amendments
[2060–AV59]
Legal Authority: 42 U.S.C. 7401 et seq.
Clean Air Act; 42 U.S.C. 7414, 7601
Abstract: This action will amend the
Lime Manufacturing National Emission
Standards for Hazardous Air Pollutants
(NESHAP), 40 CFR part 63, subpart
AAAAA, as required by the Clean Air
Act (CAA). This action will address
Louisiana Environmental Action
Network v. EPA, 955 F.3d 1088 (D.C.
Cir. 2020) (LEAN’’), in which the court
held that EPA must set limits on
uncontrolled hazardous air pollutant
(HAP) emissions when the Agency
conducts technology reviews under
CAA section 112(d)(6), 42 U.S.C.
7412(d)(6). The Lime Manufacturing
NESHAP was promulgated pursuant to
section 112(d) of the CAA on January 5,
2004. The residual risk and technology
review (RTR) was promulgated pursuant
to CAA 112(f) and 112(d)(6) on July 24,
2020. The NESHAP establishes emission
limitations based on maximum
achievable control technology for
control of HAP from kilns at new and
existing lime manufacturing plants. The
HAP emitted from lime manufacturing
kilns include hydrochloric acid,
mercury, organic HAP, and dioxins/
furans. On July 21, 2023, the U.S.
District Court for the District of
Columbia extended the deadline for
EPA to complete final action on the
Lime NESHAP to June 30, 2024. The
EPA convened a Small Business
Advocacy Review (SBAR) Panel to
obtain advice and recommendations
from small entity representatives (SERs)
that could be subject to the Lime
Manufacturing NESHAP requirements.
On August 3, 2023, the EPA’s Small
Business Advocacy Chairperson
convened the Panel, which consisted of
the Chairperson, the Director of the
Sector Policies and Programs Division
within the EPA’s Office of Air Quality
Planning and Standards, the
Administrator of the Office of
Information and Regulatory Affairs
within OMB, and the Chief Counsel for
Advocacy of the Small Business
Administration (SBA).
Timetable:
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Date
01/05/23
02/09/24
FR Cite
88 FR 805
89 FR 9088
07/00/24
Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Brian Storey,
Environmental Protection Agency,
Office of Air and Radiation, 109 T.W.
Alexander Drive, Mail Code D243–04,
Research Triangle Park, NC 27711,
Phone: 919 541–1103, Fax: 919 541–
4991, Email: storey.brian@epa.gov.
Keith Barnett, Environmental
Protection Agency, Office of Air and
Radiation, D243–04, Research Triangle
Park, NC 27711, Phone: 919 541–5605,
Fax: 919 541–4991, Email:
barnett.keith@epa.gov.
RIN: 2060–AV59
ENVIRONMENTAL PROTECTION
AGENCY (EPA)
10—Clean Air Act
Completed Actions
201. National Emission Standards for
Hazardous Air Pollutants: Ethylene
Oxide Emissions Standards for
Sterilization Facilities Residual Risk
and Technology Review [2060–AU37]
Legal Authority: 42 U.S.C. 7607(d); 42
U.S.C. 7414, 7601
Abstract: In December 1994, pursuant
to section 112(d) of the Clean Air Act,
EPA promulgated the National Emission
Standards for Hazardous Air Pollutants
(NESHAP) for Ethylene Oxide (EtO)
Commercial Sterilization and
Fumigation Operations (59 FR 62585).
The NESHAP established standards for
both major and area sources. EPA
completed a residual risk and
technology review for the NESHAP in
2006 and, at that time, concluded that
no revisions to the standards were
necessary. In this action, EPA
conducted the second RTR for the
NESHAP and updated the rule. To aid
in this effort, EPA issued an advance
notice of proposed rulemaking that
solicited comment from stakeholders,
undertook a Small Business Advocacy
Review panel, which is needed when
there is the potential for significant
economic impacts to small businesses
from any regulatory actions being
considered, and has conducted outreach
meetings within the communities
affected by the highest-risk facilities as
part of the development of this action.
These meetings involved informing
community members of the risk from
EtO emissions and explaining how they
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can be involved in the rule writing
process. EPA also held a national
webinar on this proposal.
Accommodations were made for
Spanish-language speaking
communities, which are
disproportionately affected by these EtO
emissions. This final rule also reflects
feedback EPA received from
representatives of local and state
governments. For more information,
please visit https://www.epa.gov/
stationary-sources-air-pollution/
ethylene-oxide-emissions-standardssterilization-facilities.
Timetable:
Action
ANPRM ...............
NPRM ..................
Final Rule ............
Final Rule Effective.
Date
12/12/19
04/13/23
04/05/24
04/05/24
FR Cite
84 FR 67889
88 FR 22790
89 FR 24090
Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Jon Witt,
Environmental Protection Agency,
Office of Air and Radiation, 109 T.W.
Alexander Drive, Mail Code E143–05,
Research Triangle Park, NC 27709,
Phone: 919 541–5645, Email: witt.jon@
epa.gov.
Kusondra King, Environmental
Protection Agency, Office of Air and
Radiation, Research Triangle Park, NC
27711, Phone: 919 541–4373, Email:
king.kusondra@epa.gov.
RIN: 2060–AU37
202. NSPS for GHG Emissions From
New, Modified, and Reconstructed
Fossil Fuel-Fired EGUS; Emission
Guidelines for GHG Emissions From
Existing Fossil Fuel-Fired EGUS; and
Repeal of the ACE Rule [2060–AV09]
Legal Authority: 42 U.S.C. 7411 Clean
Air Act; 42 U.S.C. 7414, 7601
Abstract: EPA has issued final carbon
pollution standards for power plants
that set carbon dioxide (CO2) limits for
new gas-fired combustion turbines and
CO2 emission guidelines for existing
coal, oil and gas-fired steam generating
units, securing important climate
benefits and protecting public health.
These rules will significantly reduce
greenhouse gas (GHG) emissions from
existing coal-fired power plants and
from new natural gas turbines, ensuring
that all long-term coal-fired plants and
base load new gas-fired plants control
90% of their carbon pollution. Existing
coal-fired power plants are the largest
source of GHGs from the power sector.
New natural gas-fired combustion
turbines are some of the largest new
sources of GHG being built today and
these final standards will ensure that
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they are constructed to minimize their
GHG emissions. Consistent with EPA’s
traditional approach to establishing
pollution standards under the Clean Air
Act, the final limits and emission
guidelines are based on proven
pollution control technologies that can
be applied directly to power plants and
can achieve substantial reductions in
carbon pollution at reasonable cost.
Emission guidelines for the longestrunning existing coal units and
performance standards for new base
load combustion turbines are based on
the use of carbon capture and
sequestration/storage (CCS) an available
and cost-effective control technology
that can be applied directly to power
plants. EPA has evaluated the emissions
reductions, benefits, and costs of the
final carbon pollution standards in a
Regulatory Impact Analysis (RIA). The
RIA projects reductions of 1.38 billion
metric tons of CO2 systemwide through
2047 along with tens of thousands of
tons of PM2.5, SO2, and NOX harmful air
pollutants that are known to endanger
public health.
Timetable:
Action
Date
NPRM ..................
Supplemental
NPRM.
Final Rule ............
Final Rule Effective.
FR Cite
05/23/23
11/20/23
88 FR 33240
88 FR 80682
05/09/24
07/08/24
89 FR 39798
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Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Lisa Thompson,
Environmental Protection Agency,
Office of Air and Radiation, 109 T.W.
Alexander Drive, Mail Code D243–01,
Research Triangle Park, NC 27711,
Phone: 919 541–9775, Email:
thompson.lisa@epa.gov.
Nick Hutson, Environmental
Protection Agency, Office of Air and
Radiation, 109 T.W. Alexander Drive,
Mail Code D243–01, Research Triangle
Park, NC 27711, Phone: 919 541–2968,
Fax: 919 541–4991, Email: hutson.nick@
epa.gov.
RIN: 2060–AV09
203. Standards of Performance for New,
Reconstructed, and Modified Sources
and Emissions Guidelines for Existing
Sources: Oil and Natural Gas Sector
Climate Review [2060–AV16]
Legal Authority: 42 U.S.C. 7411
Abstract: On November 15, 2021, the
EPA proposed new source performance
standards and emission guidelines for
crude oil and natural gas facilities. (86
FR 63110). This action was in response
to the January 20, 2021, Executive Order
titled ‘‘Protecting Public Health and the
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Environment and Restoring Science to
Tackle the Climate Crisis.’’ On
December 6, 2022, in a supplemental
proposal, EPA proposed to update,
strengthen, and expand its November
2021 proposal that would secure major
climate and health benefits for all
Americans by reducing emissions of
methane and other harmful air pollution
from both new and existing sources in
the oil and natural gas industry (87 FR
74702). On November 30, 2023, the EPA
Administrator signed the final rule
which includes multiple actions to
reduce air pollution emissions from the
Crude Oil and Natural Gas source
category. First, the EPA finalized new
source performance standards regulating
greenhouse gases and volatile organic
compounds emissions from the Crude
Oil and Natural Gas source category
pursuant to the Clean Air Act. Second,
the EPA finalized emission guidelines
under the Clean Air Act for states to
follow in developing, submitting, and
implementing state plans to establish
performance standards to limit
greenhouse gas emissions from existing
sources (designated facilities) in the
Crude Oil and Natural Gas source
category. Third, the EPA finalized
several related actions stemming from
the joint resolution of Congress, adopted
on June 30, 2021, under the
Congressional Review Act, disapproving
the EPA’s final rule titled, ‘‘Oil and
Natural Gas Sector: Emission Standards
for New, Reconstructed, and Modified
Sources Review,’’ September 14, 2020.
Fourth, the EPA finalized a protocol
under the general provisions for optical
gas imaging. The final rule was
published on March 8, 2024 (89 FR
16820).
Timetable:
Action
Date
NPRM ..................
Supplemental
NPRM.
Final Rule ............
Final Rule Effective.
FR Cite
11/15/21
12/06/22
86 FR 63110
87 FR 74702
03/08/24
05/07/24
89 FR 16820
Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Amy Hambrick,
Environmental Protection Agency,
Office of Air and Radiation, 109 T.W.
Alexander Drive, Mail Code E143–05,
Research Triangle Park, NC 27711,
Phone: 919 541–0964, Fax: 919 541–
0516, Email: hambrick.amy@epa.gov.
RIN: 2060–AV16
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204. Section 610 Review of Control of
Air Pollution From Motor Vehicles:
Tier 3 Motor Vehicle Emission and Fuel
Standards (Completion of a Section 610
Review) [2060–AV90]
Legal Authority: 5 U.S.C. 610
Abstract: The rulemaking ‘‘Control of
Air Pollution From Motor Vehicles: Tier
3 Motor Vehicle Emission and Fuel
Standards’’ was finalized by EPA in
April 2014 (79 FR 23414). The final rule
established the Tier 3 Motor Vehicle
Emission and Fuel Standards program.
The Tier 3 program was part of a
comprehensive approach to reducing
the impacts of motor vehicles on air
quality and public health. The program
considered the vehicle and its fuel as an
integrated system, setting new vehicle
emissions standards and a new gasoline
sulfur standard beginning in 2017. The
vehicle emissions standards were
expected to reduce both tailpipe and
evaporative emissions from passenger
cars, light-duty trucks, medium-duty
passenger vehicles, and some heavyduty vehicles. The gasoline sulfur
standards were expected to enable more
stringent vehicle emissions standards
and to make emissions control systems
more effective. This entry in the
regulatory agenda announces that the
EPA has reviewed this action pursuant
to section 610 of the Regulatory
Flexibility Act (5 U.S.C. 610) to
determine if the provisions that could
affect small entities should be continued
without change or should be rescinded
or amended to minimize adverse
economic impacts on small entities. As
part of this review, the EPA solicited
comments on the following factors: (1)
The continued need for the rule; (2) the
nature of complaints or comments
received concerning the rule; (3) the
complexity of the rule; (4) the extent to
which the rule overlaps, duplicates, or
conflicts with other Federal, State, or
local government rules; and (5) the
degree to which the technology,
economic conditions or other factors
have changed in the area affected by the
rule. No comments were received. The
EPA has concluded that the rule does
not need to be amended at this time and
has addressed the review factors in a
report. The report is available in Docket
EPA–HQ–OAR–2011–0135, which can
be accessed at www.regulations.gov.
Timetable:
Action
Final Rule ............
Begin Review ......
End Review .........
Date
04/28/14
07/27/23
05/15/24
FR Cite
79 FR 23414
88 FR 48598
Regulatory Flexibility Analysis
Required: No.
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Agency Contact: Jessica Mroz,
Environmental Protection Agency,
Office of Air and Radiation, 1200
Pennsylvania Avenue NW, Washington,
DC 20460, Phone: 202 564–1094, Email:
mroz.jessica@epa.gov.
RIN: 2060–AV90
ENVIRONMENTAL PROTECTION
AGENCY (EPA)
35—TSCA
Proposed Rule Stage
205. 1-Bromopropane (1–BP);
Regulation Under the Toxic Substances
Control Act (TSCA) [2070–AK73]
Legal Authority: 15 U.S.C. 2605 Toxic
Substances Control Act
Abstract: This proposed rulemaking
will address the unreasonable risk of
injury to health presented by 1bromopropane (1–BP). Section 6(a) of
the Toxic Substances Control Act
(TSCA) requires EPA address by rule
any unreasonable risk identified in a
TSCA risk evaluation and apply
requirements to the extent necessary so
the chemical no longer presents
unreasonable risk. The Agency’s
development of this rule incorporates
significant stakeholder outreach and
public participation, including over 40
external meetings as well as required
Federalism, Tribal, and Environmental
Justice consultations and a Small
Businesses Advocacy Review Panel.
Specifically, EPA engaged in
discussions with industry, nongovernmental organizations, other
government agencies, technical experts
and users of 1–BP, and the general
public to hear from users, academics,
manufacturers, and members of the
public health community about
practices related to commercial uses of
1–BP. EPA’s risk evaluation for 1–BP,
describing the conditions of use, is in
docket EPA–HQ–OPPT–2019–0235,
with the 2022 unreasonable risk
determination and additional materials
in docket EPA–HQ–OPPT–2016–0741.
Timetable:
Action
Date
lotter on DSK11XQN23PROD with PROPOSALS12
NPRM ..................
Final Rule ............
FR Cite
07/00/24
08/00/25
Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Amy Shuman,
Environmental Protection Agency,
Office of Chemical Safety and Pollution
Prevention, 1200 Pennsylvania Avenue
NW, Mail Code 7404M, Washington, DC
20460, Phone: 202 564–2978, Email:
shuman.amy@epa.gov.
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Joel Wolf, Environmental Protection
Agency, Office of Chemical Safety and
Pollution Prevention, 1200
Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone:
202 564–0432, Email: wolf.joel@epa.gov.
RIN: 2070–AK73
206. N-Methylpyrrolidone (NMP);
Regulation Under the Toxic Substances
Control Act (TSCA) [2070–AK85]
Legal Authority: 15 U.S.C. 2605 Toxic
Substances Control Act
Abstract: This proposed rulemaking
will address the unreasonable risk of
injury to health presented by nmethylpyrrolidone (NMP). Section 6(a)
of the Toxic Substances Control Act
(TSCA) requires EPA to address by rule
any unreasonable risk identified in a
TSCA section 6(b) risk evaluation by
applying requirements to the extent
necessary so the chemical no longer
presents unreasonable risk. The
Agency’s development of this rule
incorporates significant stakeholder
outreach and public participation,
including over 40 external meetings as
well as required Federalism, Tribal, and
Environmental Justice consultations and
a Small Businesses Advocacy Review
Panel. EPA’s 2020 risk evaluation for
NMP, describing its conditions of use is
in docket EPA–HQ–OPPT–2019–0236,
with the 2022 revised unreasonable risk
determination and additional materials
in docket EPA–HQ–OPPT–2016–0743.
Timetable:
Action
Date
NPRM ..................
NPRM Comment
Period End.
Final Rule ............
06/14/24
07/29/24
FR Cite
Fmt 4701
Action
NPRM ..................
Final Rule ............
Date
FR Cite
11/00/24
11/00/25
Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Carolyn Mottley,
Environmental Protection Agency,
Office of Chemical Safety and Pollution
Prevention, 1200 Pennsylvania Avenue,
Mail Code 7404M, Washington, DC
20460, Phone: 202 566–1955, Email:
mottley.carolyn@epa.gov.
Ana Corado, Environmental
Protection Agency, Office of Chemical
Safety and Pollution Prevention, 1200
Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone:
202 564–0140, Email: corado.ana@
epa.gov.
RIN: 2070–AK87
ENVIRONMENTAL PROTECTION
AGENCY (EPA)
05/00/25
207. C.I. Pigment Violet 29; Regulation
Under the Toxic Substances Control Act
(TSCA) [2070–AK87]
Legal Authority: 15 U.S.C. 2605 Toxic
Substances Control Act
Abstract: This proposed rulemaking
will address unreasonable risks of injury
Frm 00009
to health identified in the final risk
evaluation for C.I. Pigment Violet 29.
Section 6 of the Toxic Substances
Control Act (TSCA) requires EPA to
address unreasonable risks of injury to
health or the environment that the
Administrator has determined are
presented by a chemical substance
under the conditions of use. EPA’s risk
evaluation for C.I. Pigment Violet 29,
describing the conditions of use and
presenting EPA’s determination of
unreasonable risk, is in docket EPA–
HQ–OPPT–2018–0604, with revised risk
determination and additional
information in docket EPA–HQ–OPPT–
2016–0725.
Timetable:
89 FR 51134
Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Clara Hull,
Environmental Protection Agency,
Office of Chemical Safety and Pollution
Prevention, 1200 Pennsylvania Avenue
NW, Mail Code 7404M, Washington, DC
20460, Phone: 202 564–3954, Email:
hull.clara@epa.gov.
Joel Wolf, Environmental Protection
Agency, Office of Chemical Safety and
Pollution Prevention, 1200
Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone:
202 564–0432, Email: wolf.joel@epa.gov.
RIN: 2070–AK85
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35—TSCA
Final Rule Stage
208. Trichloroethylene (TCE);
Regulation Under the Toxic Substances
Control Act (TSCA) [2070–AK83]
Legal Authority: 15 U.S.C. 2605 Toxic
Substances Control Act
Abstract: On October 31, 2023, EPA
issued a proposed rule to address the
unreasonable risk of injury to human
health presented by trichloroethylene
(TCE) under its conditions of use as
documented in EPA’s November 2020
Risk Evaluation for TCE and January
2023 revised risk determination for TCE
pursuant to the Toxic Substances
Control Act (TSCA). TCE is widely used
as a solvent in a variety of industrial,
commercial and consumer applications
including for hydrofluorocarbon (HFC)
production, vapor and aerosol
degreasing, and in lubricants, greases,
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adhesives, and sealants. TSCA requires
that when EPA determines a chemical
substance presents unreasonable risk
that EPA address by rule the
unreasonable risk of injury to health or
the environment and apply
requirements to the extent necessary so
the chemical no longer presents
unreasonable risk. EPA determined that
TCE presents an unreasonable risk of
injury to health due to the significant
adverse health effects associated with
exposure to TCE, including non-cancer
effects (liver toxicity, kidney toxicity,
neurotoxicity, immunotoxicity,
reproductive toxicity, and
developmental toxicity) as well as
cancer (liver, kidney, and non-Hodgkin
lymphoma) from chronic inhalation and
dermal exposures to TCE. TCE is a
neurotoxicant and is carcinogenic to
humans by all routes of exposure. The
most sensitive adverse effects of TCE
exposure are non-cancer effects
(developmental toxicity and
immunosuppression) for acute
exposures and developmental toxicity
and autoimmunity for chronic
exposures. To address the identified
unreasonable risk, EPA is proposing to:
prohibit all manufacture (including
import), processing, and distribution in
commerce of TCE and industrial and
commercial use of TCE for all uses, with
longer compliance timeframes and
workplace controls for certain
processing and industrial and
commercial uses (including proposed
phaseouts and time-limited
exemptions); prohibit the disposal of
TCE to industrial pre-treatment,
industrial treatment, or publicly owned
treatment works, with a time-limited
exemption for cleanup projects; and
establish recordkeeping and
downstream notification requirements.
Timetable:
Action
Date
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NPRM ..................
Final Rule ............
10/31/23
09/00/24
FR Cite
88 FR 74712
Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Gabriela Rossner,
Environmental Protection Agency,
Office of Chemical Safety and Pollution
Prevention, 1200 Pennsylvania Avenue
NW, Mail Code 7404M, Washington, DC
20460, Phone: 202 564–2426, Email:
rossner.gabriela@epa.gov.
Joel Wolf, Environmental Protection
Agency, Office of Chemical Safety and
Pollution Prevention, 1200
Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone:
202 564–0432, Email: wolf.joel@epa.gov.
RIN: 2070–AK83
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209. Perchloroethylene (PCE);
Regulation Under the Toxic Substances
Control Act (TSCA) [2070–AK84]
Legal Authority: 15 U.S.C. 2605 Toxic
Substances Control Act
Abstract: On June 16, 2023, EPA
proposed a rule under the Toxic
Substances Control Act (TSCA) to
address the unreasonable risk of injury
to human health presented by
perchloroethylene (PCE). PCE is a
widely used solvent in a variety of
occupational and consumer applications
including fluorinated compound
production, petroleum manufacturing,
dry cleaning, and aerosol degreasing.
EPA determined that PCE presents an
unreasonable risk of injury to health due
to the significant adverse health effects
associated with exposure to PCE,
including neurotoxicity effects from
acute and chronic inhalation exposures
and dermal exposures, and cancer from
chronic inhalation exposures to PCE.
TSCA requires that EPA address by rule
any unreasonable risk of injury to health
or the environment identified in a TSCA
risk evaluation and apply requirements
to the extent necessary so the chemical
no longer presents unreasonable risk.
PCE, also known as perc and
tetrachloroethylene, is a neurotoxicant
and a likely human carcinogen.
Neurotoxicity, in particular impaired
visual and cognitive function and
diminished color discrimination, are the
most sensitive adverse effects driving
the unreasonable risk of PCE, and other
adverse effects associated with exposure
include central nervous system
depression, kidney and liver effects,
immune system toxicity, developmental
toxicity, and cancer. To address the
identified unreasonable risk, EPA is
proposing to prohibit most industrial
and commercial uses of PCE; the
manufacture (including import),
processing, and distribution in
commerce of PCE for the prohibited
industrial and commercial uses; the
manufacture (including import),
processing, and distribution in
commerce of PCE for all consumer use;
and, the manufacture (including
import), processing, distribution in
commerce, and use of PCE in dry
cleaning and related spot cleaning
through a 10-year phaseout. For certain
conditions of use that would not be
subject to a prohibition, EPA is also
proposing to require a PCE workplace
chemical protection program that
includes requirements to meet an
inhalation exposure concentration limit
and prevent direct dermal contact. EPA
is also proposing to require prescriptive
workplace controls for laboratory use,
and to establish recordkeeping and
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Sfmt 4702
downstream notification requirements.
Additionally, EPA proposes to provide
certain time-limited exemptions from
requirements for certain critical or
essential emergency uses of PCE for
which no technically and economically
feasible safer alternative is available.
The Agency’s development of this rule
incorporated significant stakeholder
outreach and public participation,
including public webinars and over 40
external meetings as well as required
Federalism, Tribal, and Environmental
Justice consultations and a Small
Businesses Advocacy Review Panel.
EPA’s risk evaluation for PCE,
describing the conditions of use is in
docket EPA–HQ–OPPT–2019–0502,
with the 2022 unreasonable risk
determination and additional materials
in docket EPA–HQ–OPPT–2016–0732.
Timetable:
Action
NPRM ..................
Final Rule ............
Date
06/16/23
08/00/24
FR Cite
88 FR 39652
Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Kelly Summers,
Environmental Protection Agency,
Office of Chemical Safety and Pollution
Prevention, 1200 Pennsylvania Avenue
NW, Mail Code 7405M, Washington, DC
20460, Phone: 202 564–2201, Email:
summers.kelly@epa.gov.
Joel Wolf, Environmental Protection
Agency, Office of Chemical Safety and
Pollution Prevention, 1200
Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone:
202 564–0432, Email: wolf.joel@epa.gov.
RIN: 2070–AK84
ENVIRONMENTAL PROTECTION
AGENCY (EPA)
35—TSCA
Completed Actions
210. Methylene Chloride; Regulation
Under the Toxic Substances Control Act
(TSCA) [2070–AK70]
Legal Authority: 15 U.S.C. 2605 Toxic
Substances Control Act
Abstract: On May 8, 2024, EPA
promulgated a final rule to address the
unreasonable risk of injury to health
presented by methylene chloride under
its conditions of use. TSCA requires that
EPA address by rule any unreasonable
risk of injury to health or the
environment identified in a TSCA risk
evaluation and apply requirements to
the extent necessary so that the
chemical no longer presents
unreasonable risk. EPA’s final rule will,
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among other things, prevent serious
illness and death associated with
uncontrolled exposures to the chemical
by preventing consumer access to the
chemical, restricting the industrial and
commercial use of the chemical while
also allowing for a reasonable transition
period where an industrial and
commercial use of the chemical is being
prohibited, provide a time-limited
exemption for a critical or essential use
of methylene chloride for which no
technically and economically feasible
safer alternative is available, and protect
workers from the unreasonable risk of
methylene chloride while on the job.
Timetable:
Action
Date
NPRM ..................
Final Rule ............
Final Rule Effective.
05/03/23
05/08/24
07/08/24
FR Cite
88 FR 28284
89 FR 39254
lotter on DSK11XQN23PROD with PROPOSALS12
Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Ingrid Feustel,
Environmental Protection Agency,
Office of Chemical Safety and Pollution
Prevention, Mail Code 7404M, 1200
Pennsylvania Avenue NW, Washington,
DC 20460, Phone: 202 564–3199, Email:
feustel.ingrid@epa.gov.
Joel Wolf, Environmental Protection
Agency, Office of Chemical Safety and
Pollution Prevention, 1200
Pennsylvania Avenue NW, Mail Code
VerDate Sep<11>2014
22:10 Aug 15, 2024
Jkt 250001
7404M, Washington, DC 20460, Phone:
202 564–0432, Email: wolf.joel@epa.gov.
RIN: 2070–AK70
ENVIRONMENTAL PROTECTION
AGENCY (EPA)
72—SDWA
Completed Actions
211. PFAS National Primary Drinking
Water Regulation Rulemaking [2040–
AG18]
Legal Authority: 42 U.S.C. 300f et seq.
Safe Drinking Water Act
Abstract: On March 3, 2021, the
Environmental Protection Agency (EPA)
published the Fourth Regulatory
Determinations in the Federal Register,
including a determination to regulate
perfluorooctanoic acid (PFOA) and
perfluorooctanesulfonic acid (PFOS) in
drinking water. Per the Safe Drinking
Water Act, following publication of the
Regulatory Determination, the
Administrator shall propose a maximum
contaminant level goal (MCLG) and a
national primary drinking water
regulation (NPDWR) not later than 24
months after determination and
promulgate a NPDWR within 18 months
after proposal (the statute authorizes a
9-month extension of this promulgation
date). The EPA issued a proposed
national primary drinking water
regulation for PFOA and PFOS as well
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66875
as other PFAS on March 29, 2023, as
part of this action. Finalization of the
NPDWR reflects a key commitment in
the EPA’s ‘‘PFAS Strategic Roadmap:
EPA’s Commitments to Action 2021–
2024.’’ EPA held a public hearing on the
proposed NPDWR on May 4, 2023. The
public comment period closed May 30,
2023, and more than 120,000 comments
were received. On April 8, 2024, the
final PFAS NPDWR was signed by the
EPA Administrator and published in the
Federal Register on April 26, 2024.
Timetable:
Action
Notice ..................
NPRM ..................
Final Rule ............
Final Rule Effective.
Date
02/09/22
03/29/23
04/26/24
06/25/24
FR Cite
87 FR 7412
88 FR 18638
89 FR 32532
Regulatory Flexibility Analysis
Required: Yes.
Agency Contact: Ryan Albert,
Environmental Protection Agency,
Office of Water, 4203M, Washington, DC
20460, Phone: 202 564–0763, Email:
albert.ryan@epa.gov.
Alexis Lan, Environmental Protection
Agency, Office of Water, 1200
Pennsylvania Avenue NW, 4601M,
Washington, DC 20460, Phone: 202 564–
0841, Email: lan.alexis@epa.gov.
RIN: 2040–AG18
[FR Doc. 2024–16459 Filed 8–15–24; 8:45 am]
BILLING CODE 6560–50–P
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Agencies
[Federal Register Volume 89, Number 159 (Friday, August 16, 2024)]
[Unknown Section]
[Pages 66866-66875]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-16459]
[[Page 66865]]
Vol. 89
Friday,
No. 159
August 16, 2024
Part XIV
Environmental Protection Agency
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Semiannual Regulatory Agenda
Federal Register / Vol. 89 , No. 159 / Friday, August 16, 2024 / UA:
Reg Flex Agenda
[[Page 66866]]
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ENVIRONMENTAL PROTECTION AGENCY
40 CFR Ch. I
[FRL 11974-01-OA; EPA-HQ-OAR-2011-0135; EPA-HQ-OAR-2024-0089]
Spring 2024 Unified Agenda of Regulatory and Deregulatory Actions
AGENCY: Environmental Protection Agency.
ACTION: Semiannual Regulatory Agenda.
-----------------------------------------------------------------------
SUMMARY: The Environmental Protection Agency (EPA) publishes the
Semiannual Agenda of Regulatory and Deregulatory Actions online at
https://www.reginfo.gov to periodically update the public. This
document contains information about:
Regulations in the Semiannual Agenda that are under
development, completed, or canceled since the last agenda; and
Reviews of regulations with small business impacts under
section 610 of the Regulatory Flexibility Act (RFA).
FOR FURTHER INFORMATION CONTACT: If you have questions or comments
about a particular action, please get in touch with the agency contact
listed in each agenda entry. If you have general questions about the
Semiannual Agenda, please contact: Caryn Muellerleile
([email protected]; 202-564-2855).
Table of Contents
I. Introduction
A. The EPA's Regulatory Information
B. What key statutes and Executive Orders guide the EPA's rule
and policymaking process?
C. How can you be involved in the EPA's rule and policymaking
process?
II. Semiannual Agenda of Regulatory and Deregulatory Actions
A. What actions are included in the e-Agenda and the Regulatory
Flexibility Agenda?
B. How is the e-Agenda organized?
C. What information is in the Regulatory Flexibility Agenda and
the e-Agenda?
D. What tools are available for mining Regulatory Agenda Data
and for finding more about EPA rules and policies?
III. Review of Regulations Under Section 610 of the Regulatory
Flexibility Act
A. Reviews of Rules With Significant Impacts on a Substantial
Number of Small Entities
B. What other special attention does EPA give to the impacts of
rules on small businesses, small governments, and small nonprofit
organizations?
IV. Thank You for Collaborating With Us
SUPPLEMENTARY INFORMATION:
I. Introduction
The EPA is committed to a regulatory strategy that effectively
achieves the Agency's mission of protecting human health and the
environment. The EPA publishes the Semiannual Agenda of Regulatory and
Deregulatory Actions to update the public about regulatory activity
undertaken in support of this mission. In the Semiannual Agenda, the
EPA provides notice of our plans to review, propose, and issue
regulations. The EPA is committed to environmental protection that
benefits all communities and encourages public participation and
meaningful engagement in our regulatory activities and processes.
Additionally, the EPA's Semiannual Agenda includes information
about rules that may have a significant economic impact on a
substantial number of small entities, and review of those regulations
under the Regulatory Flexibility Act as amended.
In this document, the EPA explains in greater detail the types of
actions and information available in the Semiannual Agenda and actions
that are currently undergoing review specifically for impacts on small
entities.
A. The EPA's Regulatory Information
``E-Agenda,'' ``online regulatory agenda,'' and ``semiannual
regulatory agenda'' all refer to the same comprehensive collection of
information that, until 2007, was published in the Federal Register
(FR). Currently, this information is only available through an online
database at https://www.reginfo.gov/.
``Regulatory Flexibility Agenda'' refers to a document that
contains information about the subset of regulations that may have a
significant impact on a substantial number of small entities. We
continue to publish this document in the Federal Register pursuant to
the Regulatory Flexibility Act of 1980. This document is available at
https://www.govinfo.gov/app/collection/fr.
``Unified Regulatory Agenda'' refers to the collection of all
agencies' agendas with an introduction prepared by the Regulatory
Information Service Center facilitated by the U.S. General Services
Administration.
``Regulatory Agenda Preamble'' refers to the document you are
reading now. It appears as part of the Regulatory Flexibility Agenda
and introduces both the EPA's Regulatory Flexibility Agenda and the e-
Agenda.
``Section 610 Review'' as required by the Regulatory Flexibility
Act means a periodic review within ten years of promulgating a final
rule that has or may have a significant economic impact on a
substantial number of small entities. The EPA maintains a list of these
actions at https://www.epa.gov/reg-flex/regulatory-flexibility-act-section-610-reviews. EPA is initiating one section 610 review and is
completing another with this semiannual agenda in spring 2024, as
described in section III.A. below.
B. What key statutes and Executive Orders guide the EPA's rule and
policymaking process?
Several environmental laws authorize the EPA's actions, including
but not limited to:
American Innovation and Manufacturing Act (AIM),
Clean Air Act (CAA),
Clean Water Act (CWA),
Comprehensive Environmental Response, Compensation, and
Liability Act (CERCLA, or Superfund),
Emergency Planning and Community Right-to-Know Act (EPCRA),
Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA),
Resource Conservation and Recovery Act (RCRA),
Safe Drinking Water Act (SDWA), and
Toxic Substances Control Act (TSCA).
The EPA must comply not only with environmental and other statutes,
but also with applicable administrative legal requirements that apply
to the issuance of regulations, such as the Administrative Procedure
Act (APA), the RFA as amended by the Small Business Regulatory
Enforcement Fairness Act (SBREFA), the Unfunded Mandates Reform Act
(UMRA), the Paperwork Reduction Act (PRA), the National Technology
Transfer and Advancement Act (NTTAA), and the Congressional Review Act
(CRA).
The EPA also meets a number of requirements contained in numerous
Executive Orders: 12866, ``Regulatory Planning and Review'' (58 FR
51735, Oct. 4, 1993), as supplemented by Executive Order 13563,
``Improving Regulation and Regulatory Review'' (76 FR 3821, Jan. 21,
2011) and amended by Executive Order 14094, ``Modernizing Regulatory
Review'' (88 FR 21879, April 11, 2023); 12898, ``Environmental
Justice'' (59 FR 7629, Feb. 16, 1994) and 14096, ``Revitalizing Our
Nation's Commitment to Environmental Justice for All'' (88 FR 25251,
April 26, 2023); 13045, ``Children's Health Protection'' (62 FR 19885,
Apr. 23, 1997); 13132, ``Federalism'' (64 FR 43255, Aug. 10, 1999);
13175, ``Consultation and Coordination with Indian Tribal Governments''
(65 FR 67249, Nov. 9, 2000); and 13211, ``Actions Concerning
Regulations That Significantly Affect Energy Supply, Distribution, or
Use'' (66 FR 28355, May 22, 2001).
[[Page 66867]]
C. How can you be involved in the EPA's rule and policymaking process?
You can make your voice heard by getting in touch with the contact
person provided in each agenda entry. The EPA encourages you to
participate as early in the process as possible. You may also
participate by commenting on proposed rules published in the Federal
Register.
Instructions on how to submit your comments through https://www.regulations.gov are provided in each Notice of Proposed Rulemaking
(NPRM). To be most effective, comments should contain information and
data that support your position, and you also should explain why the
EPA should incorporate your suggestion in the rule or other type of
action. You can be particularly helpful and persuasive if you provide
examples to illustrate your concerns and offer specific alternative(s)
to what has been proposed by the EPA.
The EPA believes its actions will be more cost effective and
protective if the development process includes stakeholders working
with us to help identify the most practical and effective solutions to
environmental problems. The EPA encourages you to become involved in
its rule- and policymaking processes. For more information about the
EPA's efforts to increase transparency, participation, and
collaboration in EPA activities, please visit https://www.epa.gov/laws-regulations/get-involved-epa-regulations.
II. Semiannual Agenda of Regulatory and Deregulatory Actions
A. What actions are included in the e-Agenda and the Regulatory
Flexibility Agenda?
The EPA includes key regulatory actions in the e-Agenda. However,
there is no legal significance to the omission of an item from the
agenda, and the EPA generally does not include the following categories
of actions:
Administrative actions such as delegations of authority,
changes of address, or phone numbers.
Under the CAA: Revisions to state implementation plans;
equivalent methods for ambient air quality monitoring; deletions from
the new source performance standards source categories list;
delegations of authority to states; area designations for air quality
planning purposes.
Under FIFRA: Registration-related decisions, actions
affecting the status of currently registered pesticides, and data call-
ins.
Under the Federal Food, Drug, and Cosmetic Act: Actions
regarding pesticide tolerances and food additive regulations.
Under TSCA: Licensing actions and new chemical actions.
Under RCRA: Authorization of State solid waste management
plans and hazardous waste delisting petitions.
Under the CWA: State Water Quality Standards, deletions
from the section 307(a) list of toxic pollutants, suspensions of toxic
testing requirements under the National Pollutant Discharge Elimination
System (NPDES), and delegations of NPDES authority to States.
Under SDWA: Actions on State underground injection control
programs.
Meanwhile, the Regulatory Flexibility Agenda includes:
Actions likely to have a significant economic impact on a
substantial number of small entities.
Rules the Agency has identified for review under section
610 of the RFA.
The EPA is initiating one review and completing another under
section 610 of the RFA in this Agenda. See section III.A. for further
detail.
B. How is the e-Agenda organized?
You can choose how to sort the agenda entries online by specifying
the characteristics of the entries of interest in the desired
individual data fields of the e-Agenda at https://www.reginfo.gov. You
can sort based on the following characteristics: EPA subagency (such as
Office of Water), stage of rulemaking as described in the following
paragraphs, alphabetically by title, or the Regulation Identifier
Number (RIN), which is assigned sequentially when an action is added to
the agenda.
Each entry in the agenda is associated with one of five rulemaking
stages. The rulemaking stages are:
1. Pre-rule Stage--The EPA's pre-rule actions are generally
intended to determine whether the agency should initiate rulemaking.
Pre-rulemakings may include anything that influences or leads to
rulemaking; this would include Advance Notices of Proposed Rulemaking
(ANPRMs) or analyses of the possible need for regulatory action.
2. Proposed Rule Stage--Proposed rulemaking actions include the
EPA's Notice of Proposed Rulemakings (NPRMs); these proposals are
scheduled to publish in the Federal Register within the next year.
3. Final Rule Stage--Final rulemaking actions are those actions
that the EPA is scheduled to finalize and publish in the Federal
Register within the next year.
4. Long-Term Actions--This section includes rulemakings for which
the next scheduled regulatory action (such as publication of a NPRM or
final rule) is twelve or more months into the future. We encourage you
to explore becoming involved even if an action is listed in the Long-
Term category.
5. Completed Actions--The EPA's completed actions are those that
have been promulgated and published in the Federal Register since
publication of the fall 2023 Agenda. This category also includes
actions that EPA is no longer considering and has elected to
``withdraw'' and the results of any RFA section 610 reviews.
C. What information is in the Regulatory Flexibility Agenda and the e-
Agenda?
The Regulatory Flexibility Agenda entries include only the nine
categories of information that are required by the Regulatory
Flexibility Act of 1980 and by Federal Register Agenda printing
requirements: Sequence Number, RIN, Title, Description, Statutory
Authority, Section 610 Review, if applicable, Regulatory Flexibility
Analysis Required, Schedule and Contact Person. Note that the
electronic version of the Agenda (E-Agenda) replicates each of these
actions with more extensive information, described below.
E-Agenda entries include:
Title: A brief description of the subject of the regulation. The
notation ''Section 610 Review'' follows the title if we are reviewing
the rule as part of our periodic review of existing rules under section
610 of the RFA (5 U.S.C. 610).
Priority: Each entry is placed into one of the following five
categories:
a. Significant under 3(f)(1): Under Executive Order 12866, as
amended, a rulemaking that may have an annual effect on the economy of
$200 million or more, or adversely affect in a material way the
economy, a sector of the economy, productivity, competition, jobs, the
environment, public health or safety, or State, local, territorial, or
tribal governments or communities.
b. Other Significant: A rulemaking that is not economically
significant but is considered significant for other reasons. This
category includes rules that may:
1. Create a serious inconsistency or otherwise interfere with an
action taken or planned by another agency.
2. Materially alter the budgetary impact of entitlements, grants,
user fees, or loan programs, or the rights and obligations of
recipients; or
3. Raise legal or policy issues for which centralized review would
meaningfully further the President's priorities, or the principles in
Executive Order 12866.
[[Page 66868]]
c. Substantive, Nonsignificant: A rulemaking that has substantive
impacts but is not Significant, Routine and Frequent, or Informational/
Administrative/Other.
d. Routine and Frequent: A rulemaking that is a specific case of a
recurring application of a regulatory program in the Code of Federal
Regulations. If an action that would normally be classified Routine and
Frequent is reviewed by the Office of Management and Budget (OMB) under
Executive Order 12866, then we would classify the action as either ''
Significant under 3(f)(1)'' or ``Other Significant.''
e. Informational/Administrative/Other: An action that is primarily
informational or pertains to an action outside the scope of Executive
Order 12866.
Major: A rule is ``major'' under 5 U.S.C. 801 (Pub. L. 104-121) if
it has resulted or is likely to result in an annual effect on the
economy of $100 million or more or meets other criteria specified in
the Congressional Review Act.
Unfunded Mandates: Whether the rule is covered by section 202 of
the Unfunded Mandates Reform Act of 1995 (Pub. L. 104-4). The Act
requires that, before issuing a NPRM likely to result in a mandate that
may result in expenditures by State, local, and tribal governments, in
the aggregate, or by the private sector of more than $100 million in 1
year, the agency prepare a written statement on federal mandates
addressing costs, benefits, and intergovernmental consultation.
Legal Authority: The sections of the United States Code (U.S.C.),
Public Law (Pub. L.), Executive Order (E.O.), or common name of the law
that authorizes the regulatory action.
CFR Citation: The section(s) of the Code of Federal Regulations
that would be affected by the action.
Legal Deadline: An indication of whether the rule is subject to a
statutory and/or a judicial deadline, the date of that deadline, and
whether the deadline pertains to a NPRM, a Final Action, or some other
action.
Abstract: A brief description of the problem the action will
address.
Timetable: The dates and citations (if available) for all past
steps and a projected date for at least the next step for the
regulatory action. A date displayed in the form 03/00/2025 means the
agency is predicting the month and year the action will take place but
not the day it will occur. For some entries, the timetable indicates
that the date of the next action is ``to be determined.''
Regulatory Flexibility Analysis Required: Indicates whether the EPA
has prepared or anticipates preparing a regulatory flexibility analysis
under section 603 or 604 of the RFA. Generally, such an analysis is
required for proposed or final rules subject to the RFA that the EPA
believes may have a significant economic impact on a substantial number
of small entities.
Small Entities Affected: Indicates whether the rule is anticipated
to have any effect on small businesses, small governments, or small
nonprofit organizations.
Government Levels Affected: Indicates whether the rule may have any
effect on levels of government and, if so, whether the affected
governments are federal, tribal, state, or local.
Federalism Implications: Indicates whether the action is expected
to 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.
Energy Impacts: Indicates whether the action is a significant
energy action under Executive Order 13211.
Sectors Affected: Indicates the main economic sectors regulated by
the action. The regulated parties are identified by their North
American Industry Classification System (NAICS) codes. These codes were
created by the Census Bureau for collecting, analyzing, and publishing
statistical data on the U.S. economy. There are more than 1,000 NAICS
codes for sectors in agriculture, mining, manufacturing, services, and
public administration.
International Trade Impacts: Indicates whether the action is likely
to have international trade or investment effects, or otherwise be of
international interest.
Agency Contact: The name, address, phone number, and email address
of a person who is knowledgeable about the regulation.
Additional Information: Other information about the action
including docket information.
URLs: For some actions, the internet addresses are included for
reading copies of rulemaking documents, submitting comments on
proposals, and getting more information about the rulemaking and the
program of which it is a part.
RIN: The Regulation Identifier Number is used by the OMB and the
public to identify and track rulemakings. The first four digits of the
RIN correspond to the EPA office with lead responsibility for
developing the action.
D. What tools are available for mining Regulatory Agenda Data and for
finding more about EPA rules and policies?
1. Federal Regulatory Dashboard
The https://www.reginfo.gov searchable database maintained by the
Regulatory Information Service Center and the OMB's Office of
Information and Regulatory Affairs (OIRA), allows users to view the
Regulatory Agenda database (https://www.reginfo.gov/public/do/eAgendaMain), with options for searching, displaying, and transmitting
data.
2. Subject Matter EPA Websites
Some actions listed in the Agenda include a URL for an EPA-
maintained website that provides additional information about the
action.
3. Public Dockets
When the EPA publishes either an ANPRM or a NPRM in the Federal
Register, the Agency typically establishes a docket to accumulate
materials developed throughout the development process for that
rulemaking. The docket serves as the repository for the collection of
documents or information related to that Agency's action or activity,
and is accessible both electronically or at the EPA's Docket Center
Reading Room (https://www.epa.gov/dockets). The EPA uses dockets
primarily for rulemaking actions, but dockets may also be used for
section 610 reviews and for various non-rulemaking activities, such as
Federal Register documents seeking public comments on draft guidance,
policy statements, information collection requests under the PRA, and
other non-rule activities. Docket information should be in that
action's agenda entry. All the EPA's public dockets can be located at
https://www.regulations.gov. The EPA particularly welcomes feedback on
rulemakings from communities likely to be affected by these actions.
III. Review of Regulations Under Section 610 of the Regulatory
Flexibility Act
A. Reviews of Rules With Significant Impacts on a Substantial Number of
Small Entities
Section 610 of the RFA requires that an agency review each rule
that has or will have a significant economic impact on a substantial
number of small entities within 10 years of promulgation. EPA is
initiating one section 610 review and completing another.
[[Page 66869]]
----------------------------------------------------------------------------------------------------------------
Review title RIN Docket ID No. Status
----------------------------------------------------------------------------------------------------------------
Section 610 Review of Standards of 2060-AW17 EPA-HQ-OAR-2024-0089................... Initiated.
Performance for New Residential
Wood Heaters, New Residential
Hydronic Heaters and Forced-Air
Furnaces.
Section 610 Review of the Tier 3 2060-AV90 EPA-HQ-OAR-2011-0135................... Completed.
Motor Vehicle Emission and Fuel
Standards.
----------------------------------------------------------------------------------------------------------------
B. What other special attention does the EPA give to the impacts of
rules on small businesses, small governments, and small nonprofit
organizations?
For each of the EPA's rulemakings, consideration is given to
whether there will be any adverse impact on any small entity. The EPA
attempts to fit the regulatory requirements, to the extent feasible, to
the scale of the businesses, organizations, and governmental
jurisdictions subject to the regulation.
Under the RFA as amended by SBREFA, the Agency must prepare a
formal analysis of the potential negative impacts on small entities,
convene a Small Business Advocacy Review Panel (proposed rule stage),
and prepare a Small Entity Compliance Guide (final rule stage) unless
the Agency certifies a rule will not have a significant economic impact
on a substantial number of small entities. For more detailed and
current information about the Agency's policy and practice with respect
to implementing the RFA/SBREFA, including ongoing Small Business
Advocacy Review Panels, please visit the EPA's RFA/SBREFA website at
https://www.epa.gov/reg-flex.
IV. Thank You for Collaborating With Us
We would like to thank those of you who choose to join with us in
making progress on the complex issues involved in protecting human
health and the environment through engaging in our rulemaking process.
Collaborative efforts such as the EPA's open rulemaking processes are
valuable tools for implementing our legal requirements to address
environmental and public health challenges. Our regulatory agenda and
your engagement play an important role in that process.
Victoria Arroyo,
Associate Administrator, Office of Policy.
10--Clean Air Act--Prerule Stage
------------------------------------------------------------------------
Regulation
Sequence No. Title Identifier No.
------------------------------------------------------------------------
198....................... 610 Review of Standards of 2060-AW17
Performance for New
Residential Wood Heaters,
New Residential Hydronic
Heaters and Forced-Air
Furnaces (Section 610
Review).
------------------------------------------------------------------------
10--Clean Air Act--Final Rule Stage
------------------------------------------------------------------------
Regulation
Sequence No. Title Identifier No.
------------------------------------------------------------------------
199....................... Revisions to the Air 2060-AV41
Emission Reporting
Requirements (AERR).
200....................... National Emission 2060-AV59
Standards for Hazardous
Air Pollutants: Lime
Manufacturing Plants;
Amendments.
------------------------------------------------------------------------
10--Clean Air Act--Completed Actions
------------------------------------------------------------------------
Regulation
Sequence No. Title Identifier No.
------------------------------------------------------------------------
201....................... National Emission 2060-AU37
Standards for Hazardous
Air Pollutants: Ethylene
Oxide Emissions Standards
for Sterilization
Facilities Residual Risk
and Technology Review.
202....................... NSPS for GHG Emissions 2060-AV09
from New, Modified, and
Reconstructed Fossil Fuel-
Fired EGUs; Emission
Guidelines for GHG
Emissions from Existing
Fossil Fuel-Fired EGUs;
and Repeal of the ACE
Rule.
203....................... Standards of Performance 2060-AV16
for New, Reconstructed,
and Modified Sources and
Emissions Guidelines for
Existing Sources: Oil and
Natural Gas Sector
Climate Review.
204....................... Section 610 Review of 2060-AV90
Control of Air Pollution
From Motor Vehicles: Tier
3 Motor Vehicle Emission
and Fuel Standards
(Completion of a Section
610 Review).
------------------------------------------------------------------------
35--TSCA--Proposed Rule Stage
------------------------------------------------------------------------
Regulation
Sequence No. Title Identifier No.
------------------------------------------------------------------------
205....................... 1-Bromopropane (1-BP); 2070-AK73
Regulation Under the
Toxic Substances Control
Act (TSCA).
206....................... N-Methylpyrrolidone (NMP); 2070-AK85
Regulation Under the
Toxic Substances Control
Act (TSCA).
207....................... C.I. Pigment Violet 29; 2070-AK87
Regulation Under the
Toxic Substances Control
Act (TSCA).
------------------------------------------------------------------------
[[Page 66870]]
35--TSCA--Final Rule Stage
------------------------------------------------------------------------
Regulation
Sequence No. Title Identifier No.
------------------------------------------------------------------------
208....................... Trichloroethylene (TCE); 2070-AK83
Regulation Under the
Toxic Substances Control
Act (TSCA).
209....................... Perchloroethylene (PCE); 2070-AK84
Regulation Under the
Toxic Substances Control
Act (TSCA).
------------------------------------------------------------------------
35--TSCA--Completed Actions
------------------------------------------------------------------------
Regulation
Sequence No. Title Identifier No.
------------------------------------------------------------------------
210....................... Methylene Chloride; 2070-AK70
Regulation Under the
Toxic Substances Control
Act (TSCA).
------------------------------------------------------------------------
72--SDWA--Completed Actions
------------------------------------------------------------------------
Regulation
Sequence No. Title Identifier No.
------------------------------------------------------------------------
211....................... PFAS National Primary 2040-AG18
Drinking Water Regulation
Rulemaking.
------------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY (EPA)
10--Clean Air Act
Prerule Stage
198. 610 Review of Standards of Performance for New
Residential Wood Heaters, New Residential Hydronic Heaters and Forced-
Air Furnaces (Section 610 Review) [2060-AW17]
Legal Authority: 42 U.S.C. 7411
Abstract: On March 16, 2015, EPA published a final rule that made
revisions to the New Source Performance Standards (NSPS) for new
residential wood heaters (80 FR 13672). The 2015 final rule (40 CFR
part 60, subpart AAA and QQQQ) updated the 1988 NSPS to reflect
significant advancements in wood heater technologies and design,
broadened the range of residential wood-heating appliances covered by
the regulation, and improved and streamlined implementation procedures.
The 2015 rule requires manufacturers to redesign wood heaters to be
cleaner and lower emitting. In general, the design changes also make
the heaters perform better and more efficiently. This new entry in the
regulatory agenda announces that EPA will review the March 16, 2015
action pursuant to section 610 of the Regulatory Flexibility Act (5
U.S.C. 610) to determine if the provisions that could affect small
entities should be maintained or should be rescinded or amended to
minimize adverse economic impacts on small entities. As part of this
review, EPA will consider and solicit comments on the following: (1)
The continued need for the rule; (2) the nature of complaints or
comments received concerning the rule; (3) the complexity of the rule;
(4) the extent to which the rule overlaps, duplicates, or conflicts
with other Federal, State, or local government rules; and (5) the
degree to which the technology, economic conditions or other factors
have changed in the area affected by the rule. Comments must be
received within 60 days of this notice. In submitting comments, please
reference Docket ID EPA-HQ-OAR-2024-0089 and follow the instructions
provided in the preamble to this issue of the Regulatory Agenda. This
docket can be accessed at www.regulations.gov.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
Final Rule.......................... 03/16/15 80 FR 13672
Begin Review........................ 07/00/24 .......................
End Review.......................... 11/00/24 .......................
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: No.
Agency Contact: Bill Schrock, Environmental Protection Agency,
Office of Air and Radiation, 109 T.W. Alexander Drive, Mail Code E143-
03, Research Triangle Park, NC 27711, Phone: 919 541-5032, Email:
[email protected].
Nicholas Swanson, Environmental Protection Agency, Office of Air
and Radiation, E143-03, Research Triangle Park, NC 27711, Phone: 919
541-4080, Email: [email protected].
RIN: 2060-AW17
ENVIRONMENTAL PROTECTION AGENCY (EPA)
10--Clean Air Act
Final Rule Stage
199. Revisions to the Air Emission Reporting Requirements (AERR) [2060-
AV41]
Legal Authority: 42 U.S.C. 7401 et seq. Clean Air Act
Abstract: This action finalizes changes to the Environmental
Protection Agency's (EPA) emissions inventory reporting requirements to
collect data needed for the EPA to implement pollution reduction
programs and address environmental justice concerns. The amendments in
this action would ensure that the EPA has sufficient information to
identify and solve air quality and exposure problems. The amendments
would also allow the EPA to have information readily available that the
Agency needs to protect public health and perform other activities
under the Clean Air Act (CAA or ``the Act''). Further, the amendments
would ensure that communities have the data needed to understand
significant sources of air pollution that may be impacting them--
including potent carcinogens and other highly toxic chemicals linked
with a wide range of chronic and acute health problems.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
NPRM................................ 08/09/23 88 FR 54118
Notice.............................. 10/12/23 88 FR 63046
Final Rule.......................... 07/00/24 .......................
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
[[Page 66871]]
Agency Contact: Marc Houyoux, Environmental Protection Agency,
Office of Air and Radiation, C339-02, Research Triangle Park, NC 27711,
Phone: 919 541-3649, Fax: 919 541-0684, Email: [email protected].
RIN: 2060-AV41
200. National Emission Standards for Hazardous Air Pollutants: Lime
Manufacturing Plants; Amendments [2060-AV59]
Legal Authority: 42 U.S.C. 7401 et seq. Clean Air Act; 42 U.S.C.
7414, 7601
Abstract: This action will amend the Lime Manufacturing National
Emission Standards for Hazardous Air Pollutants (NESHAP), 40 CFR part
63, subpart AAAAA, as required by the Clean Air Act (CAA). This action
will address Louisiana Environmental Action Network v. EPA, 955 F.3d
1088 (D.C. Cir. 2020) (LEAN''), in which the court held that EPA must
set limits on uncontrolled hazardous air pollutant (HAP) emissions when
the Agency conducts technology reviews under CAA section 112(d)(6), 42
U.S.C. 7412(d)(6). The Lime Manufacturing NESHAP was promulgated
pursuant to section 112(d) of the CAA on January 5, 2004. The residual
risk and technology review (RTR) was promulgated pursuant to CAA 112(f)
and 112(d)(6) on July 24, 2020. The NESHAP establishes emission
limitations based on maximum achievable control technology for control
of HAP from kilns at new and existing lime manufacturing plants. The
HAP emitted from lime manufacturing kilns include hydrochloric acid,
mercury, organic HAP, and dioxins/furans. On July 21, 2023, the U.S.
District Court for the District of Columbia extended the deadline for
EPA to complete final action on the Lime NESHAP to June 30, 2024. The
EPA convened a Small Business Advocacy Review (SBAR) Panel to obtain
advice and recommendations from small entity representatives (SERs)
that could be subject to the Lime Manufacturing NESHAP requirements. On
August 3, 2023, the EPA's Small Business Advocacy Chairperson convened
the Panel, which consisted of the Chairperson, the Director of the
Sector Policies and Programs Division within the EPA's Office of Air
Quality Planning and Standards, the Administrator of the Office of
Information and Regulatory Affairs within OMB, and the Chief Counsel
for Advocacy of the Small Business Administration (SBA).
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
NPRM................................ 01/05/23 88 FR 805
Supplemental NPRM................... 02/09/24 89 FR 9088
Final Rule.......................... 07/00/24 .......................
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Brian Storey, Environmental Protection Agency,
Office of Air and Radiation, 109 T.W. Alexander Drive, Mail Code D243-
04, Research Triangle Park, NC 27711, Phone: 919 541-1103, Fax: 919
541-4991, Email: [email protected].
Keith Barnett, Environmental Protection Agency, Office of Air and
Radiation, D243-04, Research Triangle Park, NC 27711, Phone: 919 541-
5605, Fax: 919 541-4991, Email: [email protected].
RIN: 2060-AV59
ENVIRONMENTAL PROTECTION AGENCY (EPA)
10--Clean Air Act
Completed Actions
201. National Emission Standards for Hazardous Air Pollutants: Ethylene
Oxide Emissions Standards for Sterilization Facilities Residual Risk
and Technology Review [2060-AU37]
Legal Authority: 42 U.S.C. 7607(d); 42 U.S.C. 7414, 7601
Abstract: In December 1994, pursuant to section 112(d) of the Clean
Air Act, EPA promulgated the National Emission Standards for Hazardous
Air Pollutants (NESHAP) for Ethylene Oxide (EtO) Commercial
Sterilization and Fumigation Operations (59 FR 62585). The NESHAP
established standards for both major and area sources. EPA completed a
residual risk and technology review for the NESHAP in 2006 and, at that
time, concluded that no revisions to the standards were necessary. In
this action, EPA conducted the second RTR for the NESHAP and updated
the rule. To aid in this effort, EPA issued an advance notice of
proposed rulemaking that solicited comment from stakeholders, undertook
a Small Business Advocacy Review panel, which is needed when there is
the potential for significant economic impacts to small businesses from
any regulatory actions being considered, and has conducted outreach
meetings within the communities affected by the highest-risk facilities
as part of the development of this action. These meetings involved
informing community members of the risk from EtO emissions and
explaining how they can be involved in the rule writing process. EPA
also held a national webinar on this proposal. Accommodations were made
for Spanish-language speaking communities, which are disproportionately
affected by these EtO emissions. This final rule also reflects feedback
EPA received from representatives of local and state governments. For
more information, please visit https://www.epa.gov/stationary-sources-air-pollution/ethylene-oxide-emissions-standards-sterilization-facilities.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
ANPRM............................... 12/12/19 84 FR 67889
NPRM................................ 04/13/23 88 FR 22790
Final Rule.......................... 04/05/24 89 FR 24090
Final Rule Effective................ 04/05/24 .......................
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Jon Witt, Environmental Protection Agency, Office
of Air and Radiation, 109 T.W. Alexander Drive, Mail Code E143-05,
Research Triangle Park, NC 27709, Phone: 919 541-5645, Email:
[email protected].
Kusondra King, Environmental Protection Agency, Office of Air and
Radiation, Research Triangle Park, NC 27711, Phone: 919 541-4373,
Email: [email protected].
RIN: 2060-AU37
202. NSPS for GHG Emissions From New, Modified, and Reconstructed
Fossil Fuel-Fired EGUS; Emission Guidelines for GHG Emissions From
Existing Fossil Fuel-Fired EGUS; and Repeal of the ACE Rule [2060-AV09]
Legal Authority: 42 U.S.C. 7411 Clean Air Act; 42 U.S.C. 7414, 7601
Abstract: EPA has issued final carbon pollution standards for power
plants that set carbon dioxide (CO2) limits for new gas-
fired combustion turbines and CO2 emission guidelines for
existing coal, oil and gas-fired steam generating units, securing
important climate benefits and protecting public health. These rules
will significantly reduce greenhouse gas (GHG) emissions from existing
coal-fired power plants and from new natural gas turbines, ensuring
that all long-term coal-fired plants and base load new gas-fired plants
control 90% of their carbon pollution. Existing coal-fired power plants
are the largest source of GHGs from the power sector. New natural gas-
fired combustion turbines are some of the largest new sources of GHG
being built today and these final standards will ensure that
[[Page 66872]]
they are constructed to minimize their GHG emissions. Consistent with
EPA's traditional approach to establishing pollution standards under
the Clean Air Act, the final limits and emission guidelines are based
on proven pollution control technologies that can be applied directly
to power plants and can achieve substantial reductions in carbon
pollution at reasonable cost. Emission guidelines for the longest-
running existing coal units and performance standards for new base load
combustion turbines are based on the use of carbon capture and
sequestration/storage (CCS) an available and cost-effective control
technology that can be applied directly to power plants. EPA has
evaluated the emissions reductions, benefits, and costs of the final
carbon pollution standards in a Regulatory Impact Analysis (RIA). The
RIA projects reductions of 1.38 billion metric tons of CO2
systemwide through 2047 along with tens of thousands of tons of
PM2.5, SO2, and NOX harmful air
pollutants that are known to endanger public health.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
NPRM................................ 05/23/23 88 FR 33240
Supplemental NPRM................... 11/20/23 88 FR 80682
Final Rule.......................... 05/09/24 89 FR 39798
Final Rule Effective................ 07/08/24 .......................
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Lisa Thompson, Environmental Protection Agency,
Office of Air and Radiation, 109 T.W. Alexander Drive, Mail Code D243-
01, Research Triangle Park, NC 27711, Phone: 919 541-9775, Email:
[email protected].
Nick Hutson, Environmental Protection Agency, Office of Air and
Radiation, 109 T.W. Alexander Drive, Mail Code D243-01, Research
Triangle Park, NC 27711, Phone: 919 541-2968, Fax: 919 541-4991, Email:
[email protected].
RIN: 2060-AV09
203. Standards of Performance for New, Reconstructed, and Modified
Sources and Emissions Guidelines for Existing Sources: Oil and Natural
Gas Sector Climate Review [2060-AV16]
Legal Authority: 42 U.S.C. 7411
Abstract: On November 15, 2021, the EPA proposed new source
performance standards and emission guidelines for crude oil and natural
gas facilities. (86 FR 63110). This action was in response to the
January 20, 2021, Executive Order titled ``Protecting Public Health and
the Environment and Restoring Science to Tackle the Climate Crisis.''
On December 6, 2022, in a supplemental proposal, EPA proposed to
update, strengthen, and expand its November 2021 proposal that would
secure major climate and health benefits for all Americans by reducing
emissions of methane and other harmful air pollution from both new and
existing sources in the oil and natural gas industry (87 FR 74702). On
November 30, 2023, the EPA Administrator signed the final rule which
includes multiple actions to reduce air pollution emissions from the
Crude Oil and Natural Gas source category. First, the EPA finalized new
source performance standards regulating greenhouse gases and volatile
organic compounds emissions from the Crude Oil and Natural Gas source
category pursuant to the Clean Air Act. Second, the EPA finalized
emission guidelines under the Clean Air Act for states to follow in
developing, submitting, and implementing state plans to establish
performance standards to limit greenhouse gas emissions from existing
sources (designated facilities) in the Crude Oil and Natural Gas source
category. Third, the EPA finalized several related actions stemming
from the joint resolution of Congress, adopted on June 30, 2021, under
the Congressional Review Act, disapproving the EPA's final rule titled,
``Oil and Natural Gas Sector: Emission Standards for New,
Reconstructed, and Modified Sources Review,'' September 14, 2020.
Fourth, the EPA finalized a protocol under the general provisions for
optical gas imaging. The final rule was published on March 8, 2024 (89
FR 16820).
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
NPRM................................ 11/15/21 86 FR 63110
Supplemental NPRM................... 12/06/22 87 FR 74702
Final Rule.......................... 03/08/24 89 FR 16820
Final Rule Effective................ 05/07/24 .......................
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Amy Hambrick, Environmental Protection Agency,
Office of Air and Radiation, 109 T.W. Alexander Drive, Mail Code E143-
05, Research Triangle Park, NC 27711, Phone: 919 541-0964, Fax: 919
541-0516, Email: [email protected].
RIN: 2060-AV16
204. Section 610 Review of Control of Air Pollution From Motor
Vehicles: Tier 3 Motor Vehicle Emission and Fuel Standards (Completion
of a Section 610 Review) [2060-AV90]
Legal Authority: 5 U.S.C. 610
Abstract: The rulemaking ``Control of Air Pollution From Motor
Vehicles: Tier 3 Motor Vehicle Emission and Fuel Standards'' was
finalized by EPA in April 2014 (79 FR 23414). The final rule
established the Tier 3 Motor Vehicle Emission and Fuel Standards
program. The Tier 3 program was part of a comprehensive approach to
reducing the impacts of motor vehicles on air quality and public
health. The program considered the vehicle and its fuel as an
integrated system, setting new vehicle emissions standards and a new
gasoline sulfur standard beginning in 2017. The vehicle emissions
standards were expected to reduce both tailpipe and evaporative
emissions from passenger cars, light-duty trucks, medium-duty passenger
vehicles, and some heavy-duty vehicles. The gasoline sulfur standards
were expected to enable more stringent vehicle emissions standards and
to make emissions control systems more effective. This entry in the
regulatory agenda announces that the EPA has reviewed this action
pursuant to section 610 of the Regulatory Flexibility Act (5 U.S.C.
610) to determine if the provisions that could affect small entities
should be continued without change or should be rescinded or amended to
minimize adverse economic impacts on small entities. As part of this
review, the EPA solicited comments on the following factors: (1) The
continued need for the rule; (2) the nature of complaints or comments
received concerning the rule; (3) the complexity of the rule; (4) the
extent to which the rule overlaps, duplicates, or conflicts with other
Federal, State, or local government rules; and (5) the degree to which
the technology, economic conditions or other factors have changed in
the area affected by the rule. No comments were received. The EPA has
concluded that the rule does not need to be amended at this time and
has addressed the review factors in a report. The report is available
in Docket EPA-HQ-OAR-2011-0135, which can be accessed at
www.regulations.gov.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
Final Rule.......................... 04/28/14 79 FR 23414
Begin Review........................ 07/27/23 88 FR 48598
End Review.......................... 05/15/24
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: No.
[[Page 66873]]
Agency Contact: Jessica Mroz, Environmental Protection Agency,
Office of Air and Radiation, 1200 Pennsylvania Avenue NW, Washington,
DC 20460, Phone: 202 564-1094, Email: [email protected].
RIN: 2060-AV90
ENVIRONMENTAL PROTECTION AGENCY (EPA)
35--TSCA
Proposed Rule Stage
205. 1-Bromopropane (1-BP); Regulation Under the Toxic Substances
Control Act (TSCA) [2070-AK73]
Legal Authority: 15 U.S.C. 2605 Toxic Substances Control Act
Abstract: This proposed rulemaking will address the unreasonable
risk of injury to health presented by 1-bromopropane (1-BP). Section
6(a) of the Toxic Substances Control Act (TSCA) requires EPA address by
rule any unreasonable risk identified in a TSCA risk evaluation and
apply requirements to the extent necessary so the chemical no longer
presents unreasonable risk. The Agency's development of this rule
incorporates significant stakeholder outreach and public participation,
including over 40 external meetings as well as required Federalism,
Tribal, and Environmental Justice consultations and a Small Businesses
Advocacy Review Panel. Specifically, EPA engaged in discussions with
industry, non-governmental organizations, other government agencies,
technical experts and users of 1-BP, and the general public to hear
from users, academics, manufacturers, and members of the public health
community about practices related to commercial uses of 1-BP. EPA's
risk evaluation for 1-BP, describing the conditions of use, is in
docket EPA-HQ-OPPT-2019-0235, with the 2022 unreasonable risk
determination and additional materials in docket EPA-HQ-OPPT-2016-0741.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
NPRM................................ 07/00/24
Final Rule.......................... 08/00/25
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Amy Shuman, Environmental Protection Agency, Office
of Chemical Safety and Pollution Prevention, 1200 Pennsylvania Avenue
NW, Mail Code 7404M, Washington, DC 20460, Phone: 202 564-2978, Email:
[email protected].
Joel Wolf, Environmental Protection Agency, Office of Chemical
Safety and Pollution Prevention, 1200 Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone: 202 564-0432, Email:
[email protected].
RIN: 2070-AK73
206. N-Methylpyrrolidone (NMP); Regulation Under the Toxic Substances
Control Act (TSCA) [2070-AK85]
Legal Authority: 15 U.S.C. 2605 Toxic Substances Control Act
Abstract: This proposed rulemaking will address the unreasonable
risk of injury to health presented by n-methylpyrrolidone (NMP).
Section 6(a) of the Toxic Substances Control Act (TSCA) requires EPA to
address by rule any unreasonable risk identified in a TSCA section 6(b)
risk evaluation by applying requirements to the extent necessary so the
chemical no longer presents unreasonable risk. The Agency's development
of this rule incorporates significant stakeholder outreach and public
participation, including over 40 external meetings as well as required
Federalism, Tribal, and Environmental Justice consultations and a Small
Businesses Advocacy Review Panel. EPA's 2020 risk evaluation for NMP,
describing its conditions of use is in docket EPA-HQ-OPPT-2019-0236,
with the 2022 revised unreasonable risk determination and additional
materials in docket EPA-HQ-OPPT-2016-0743.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
NPRM................................ 06/14/24 89 FR 51134
NPRM Comment Period End............. 07/29/24
Final Rule.......................... 05/00/25
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Clara Hull, Environmental Protection Agency, Office
of Chemical Safety and Pollution Prevention, 1200 Pennsylvania Avenue
NW, Mail Code 7404M, Washington, DC 20460, Phone: 202 564-3954, Email:
[email protected].
Joel Wolf, Environmental Protection Agency, Office of Chemical
Safety and Pollution Prevention, 1200 Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone: 202 564-0432, Email:
[email protected].
RIN: 2070-AK85
207. C.I. Pigment Violet 29; Regulation Under the Toxic Substances
Control Act (TSCA) [2070-AK87]
Legal Authority: 15 U.S.C. 2605 Toxic Substances Control Act
Abstract: This proposed rulemaking will address unreasonable risks
of injury to health identified in the final risk evaluation for C.I.
Pigment Violet 29. Section 6 of the Toxic Substances Control Act (TSCA)
requires EPA to address unreasonable risks of injury to health or the
environment that the Administrator has determined are presented by a
chemical substance under the conditions of use. EPA's risk evaluation
for C.I. Pigment Violet 29, describing the conditions of use and
presenting EPA's determination of unreasonable risk, is in docket EPA-
HQ-OPPT-2018-0604, with revised risk determination and additional
information in docket EPA-HQ-OPPT-2016-0725.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
NPRM................................ 11/00/24
Final Rule.......................... 11/00/25
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Carolyn Mottley, Environmental Protection Agency,
Office of Chemical Safety and Pollution Prevention, 1200 Pennsylvania
Avenue, Mail Code 7404M, Washington, DC 20460, Phone: 202 566-1955,
Email: [email protected].
Ana Corado, Environmental Protection Agency, Office of Chemical
Safety and Pollution Prevention, 1200 Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone: 202 564-0140, Email:
[email protected].
RIN: 2070-AK87
ENVIRONMENTAL PROTECTION AGENCY (EPA)
35--TSCA
Final Rule Stage
208. Trichloroethylene (TCE); Regulation Under the Toxic Substances
Control Act (TSCA) [2070-AK83]
Legal Authority: 15 U.S.C. 2605 Toxic Substances Control Act
Abstract: On October 31, 2023, EPA issued a proposed rule to
address the unreasonable risk of injury to human health presented by
trichloroethylene (TCE) under its conditions of use as documented in
EPA's November 2020 Risk Evaluation for TCE and January 2023 revised
risk determination for TCE pursuant to the Toxic Substances Control Act
(TSCA). TCE is widely used as a solvent in a variety of industrial,
commercial and consumer applications including for hydrofluorocarbon
(HFC) production, vapor and aerosol degreasing, and in lubricants,
greases,
[[Page 66874]]
adhesives, and sealants. TSCA requires that when EPA determines a
chemical substance presents unreasonable risk that EPA address by rule
the unreasonable risk of injury to health or the environment and apply
requirements to the extent necessary so the chemical no longer presents
unreasonable risk. EPA determined that TCE presents an unreasonable
risk of injury to health due to the significant adverse health effects
associated with exposure to TCE, including non-cancer effects (liver
toxicity, kidney toxicity, neurotoxicity, immunotoxicity, reproductive
toxicity, and developmental toxicity) as well as cancer (liver, kidney,
and non-Hodgkin lymphoma) from chronic inhalation and dermal exposures
to TCE. TCE is a neurotoxicant and is carcinogenic to humans by all
routes of exposure. The most sensitive adverse effects of TCE exposure
are non-cancer effects (developmental toxicity and immunosuppression)
for acute exposures and developmental toxicity and autoimmunity for
chronic exposures. To address the identified unreasonable risk, EPA is
proposing to: prohibit all manufacture (including import), processing,
and distribution in commerce of TCE and industrial and commercial use
of TCE for all uses, with longer compliance timeframes and workplace
controls for certain processing and industrial and commercial uses
(including proposed phaseouts and time-limited exemptions); prohibit
the disposal of TCE to industrial pre-treatment, industrial treatment,
or publicly owned treatment works, with a time-limited exemption for
cleanup projects; and establish recordkeeping and downstream
notification requirements.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
NPRM................................ 10/31/23 88 FR 74712
Final Rule.......................... 09/00/24
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Gabriela Rossner, Environmental Protection Agency,
Office of Chemical Safety and Pollution Prevention, 1200 Pennsylvania
Avenue NW, Mail Code 7404M, Washington, DC 20460, Phone: 202 564-2426,
Email: [email protected].
Joel Wolf, Environmental Protection Agency, Office of Chemical
Safety and Pollution Prevention, 1200 Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone: 202 564-0432, Email:
[email protected].
RIN: 2070-AK83
209. Perchloroethylene (PCE); Regulation Under the Toxic Substances
Control Act (TSCA) [2070-AK84]
Legal Authority: 15 U.S.C. 2605 Toxic Substances Control Act
Abstract: On June 16, 2023, EPA proposed a rule under the Toxic
Substances Control Act (TSCA) to address the unreasonable risk of
injury to human health presented by perchloroethylene (PCE). PCE is a
widely used solvent in a variety of occupational and consumer
applications including fluorinated compound production, petroleum
manufacturing, dry cleaning, and aerosol degreasing. EPA determined
that PCE presents an unreasonable risk of injury to health due to the
significant adverse health effects associated with exposure to PCE,
including neurotoxicity effects from acute and chronic inhalation
exposures and dermal exposures, and cancer from chronic inhalation
exposures to PCE. TSCA requires that EPA address by rule any
unreasonable risk of injury to health or the environment identified in
a TSCA risk evaluation and apply requirements to the extent necessary
so the chemical no longer presents unreasonable risk. PCE, also known
as perc and tetrachloroethylene, is a neurotoxicant and a likely human
carcinogen. Neurotoxicity, in particular impaired visual and cognitive
function and diminished color discrimination, are the most sensitive
adverse effects driving the unreasonable risk of PCE, and other adverse
effects associated with exposure include central nervous system
depression, kidney and liver effects, immune system toxicity,
developmental toxicity, and cancer. To address the identified
unreasonable risk, EPA is proposing to prohibit most industrial and
commercial uses of PCE; the manufacture (including import), processing,
and distribution in commerce of PCE for the prohibited industrial and
commercial uses; the manufacture (including import), processing, and
distribution in commerce of PCE for all consumer use; and, the
manufacture (including import), processing, distribution in commerce,
and use of PCE in dry cleaning and related spot cleaning through a 10-
year phaseout. For certain conditions of use that would not be subject
to a prohibition, EPA is also proposing to require a PCE workplace
chemical protection program that includes requirements to meet an
inhalation exposure concentration limit and prevent direct dermal
contact. EPA is also proposing to require prescriptive workplace
controls for laboratory use, and to establish recordkeeping and
downstream notification requirements. Additionally, EPA proposes to
provide certain time-limited exemptions from requirements for certain
critical or essential emergency uses of PCE for which no technically
and economically feasible safer alternative is available. The Agency's
development of this rule incorporated significant stakeholder outreach
and public participation, including public webinars and over 40
external meetings as well as required Federalism, Tribal, and
Environmental Justice consultations and a Small Businesses Advocacy
Review Panel. EPA's risk evaluation for PCE, describing the conditions
of use is in docket EPA-HQ-OPPT-2019-0502, with the 2022 unreasonable
risk determination and additional materials in docket EPA-HQ-OPPT-2016-
0732.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
NPRM................................ 06/16/23 88 FR 39652
Final Rule.......................... 08/00/24
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Kelly Summers, Environmental Protection Agency,
Office of Chemical Safety and Pollution Prevention, 1200 Pennsylvania
Avenue NW, Mail Code 7405M, Washington, DC 20460, Phone: 202 564-2201,
Email: [email protected].
Joel Wolf, Environmental Protection Agency, Office of Chemical
Safety and Pollution Prevention, 1200 Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone: 202 564-0432, Email:
[email protected].
RIN: 2070-AK84
ENVIRONMENTAL PROTECTION AGENCY (EPA)
35--TSCA
Completed Actions
210. Methylene Chloride; Regulation Under the Toxic Substances Control
Act (TSCA) [2070-AK70]
Legal Authority: 15 U.S.C. 2605 Toxic Substances Control Act
Abstract: On May 8, 2024, EPA promulgated a final rule to address
the unreasonable risk of injury to health presented by methylene
chloride under its conditions of use. TSCA requires that EPA address by
rule any unreasonable risk of injury to health or the environment
identified in a TSCA risk evaluation and apply requirements to the
extent necessary so that the chemical no longer presents unreasonable
risk. EPA's final rule will,
[[Page 66875]]
among other things, prevent serious illness and death associated with
uncontrolled exposures to the chemical by preventing consumer access to
the chemical, restricting the industrial and commercial use of the
chemical while also allowing for a reasonable transition period where
an industrial and commercial use of the chemical is being prohibited,
provide a time-limited exemption for a critical or essential use of
methylene chloride for which no technically and economically feasible
safer alternative is available, and protect workers from the
unreasonable risk of methylene chloride while on the job.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
NPRM................................ 05/03/23 88 FR 28284
Final Rule.......................... 05/08/24 89 FR 39254
Final Rule Effective................ 07/08/24
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Ingrid Feustel, Environmental Protection Agency,
Office of Chemical Safety and Pollution Prevention, Mail Code 7404M,
1200 Pennsylvania Avenue NW, Washington, DC 20460, Phone: 202 564-3199,
Email: [email protected].
Joel Wolf, Environmental Protection Agency, Office of Chemical
Safety and Pollution Prevention, 1200 Pennsylvania Avenue NW, Mail Code
7404M, Washington, DC 20460, Phone: 202 564-0432, Email:
[email protected].
RIN: 2070-AK70
ENVIRONMENTAL PROTECTION AGENCY (EPA)
72--SDWA
Completed Actions
211. PFAS National Primary Drinking Water Regulation Rulemaking [2040-
AG18]
Legal Authority: 42 U.S.C. 300f et seq. Safe Drinking Water Act
Abstract: On March 3, 2021, the Environmental Protection Agency
(EPA) published the Fourth Regulatory Determinations in the Federal
Register, including a determination to regulate perfluorooctanoic acid
(PFOA) and perfluorooctanesulfonic acid (PFOS) in drinking water. Per
the Safe Drinking Water Act, following publication of the Regulatory
Determination, the Administrator shall propose a maximum contaminant
level goal (MCLG) and a national primary drinking water regulation
(NPDWR) not later than 24 months after determination and promulgate a
NPDWR within 18 months after proposal (the statute authorizes a 9-month
extension of this promulgation date). The EPA issued a proposed
national primary drinking water regulation for PFOA and PFOS as well as
other PFAS on March 29, 2023, as part of this action. Finalization of
the NPDWR reflects a key commitment in the EPA's ``PFAS Strategic
Roadmap: EPA's Commitments to Action 2021-2024.'' EPA held a public
hearing on the proposed NPDWR on May 4, 2023. The public comment period
closed May 30, 2023, and more than 120,000 comments were received. On
April 8, 2024, the final PFAS NPDWR was signed by the EPA Administrator
and published in the Federal Register on April 26, 2024.
Timetable:
------------------------------------------------------------------------
Action Date FR Cite
------------------------------------------------------------------------
Notice.............................. 02/09/22 87 FR 7412
NPRM................................ 03/29/23 88 FR 18638
Final Rule.......................... 04/26/24 89 FR 32532
Final Rule Effective................ 06/25/24
------------------------------------------------------------------------
Regulatory Flexibility Analysis Required: Yes.
Agency Contact: Ryan Albert, Environmental Protection Agency,
Office of Water, 4203M, Washington, DC 20460, Phone: 202 564-0763,
Email: [email protected].
Alexis Lan, Environmental Protection Agency, Office of Water, 1200
Pennsylvania Avenue NW, 4601M, Washington, DC 20460, Phone: 202 564-
0841, Email: [email protected].
RIN: 2040-AG18
[FR Doc. 2024-16459 Filed 8-15-24; 8:45 am]
BILLING CODE 6560-50-P