Rule2023-22529

Phasedown of Hydrofluorocarbons: Restrictions on the Use of Certain Hydrofluorocarbons Under the American Innovation and Manufacturing Act of 2020

Primary source

Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.

Published
October 24, 2023
Effective
December 26, 2023

Issuing agencies

Environmental Protection Agency

Abstract

The U.S. Environmental Protection Agency is issuing regulations to implement certain provisions of the American Innovation and Manufacturing Act, as enacted on December 27, 2020. This rulemaking restricts the use of hydrofluorocarbons in specific sectors or subsectors in which they are used; establishes a process for submitting technology transitions petitions; establishes recordkeeping and reporting requirements; and addresses certain other elements related to the effective implementation of the American Innovation and Manufacturing Act. These restrictions on the use of hydrofluorocarbons address petitions granted on October 7, 2021, and September 19, 2022.

Full Text

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[Federal Register Volume 88, Number 204 (Tuesday, October 24, 2023)]
[Rules and Regulations]
[Pages 73098-73212]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2023-22529]



[[Page 73097]]

Vol. 88

Tuesday,

No. 204

October 24, 2023

Part II





Environmental Protection Agency





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40 CFR Part 84





Phasedown of Hydrofluorocarbons: Restrictions on the Use of Certain 
Hydrofluorocarbons Under the American Innovation and Manufacturing Act 
of 2020; Final Rule

Federal Register / Vol. 88 , No. 204 / Tuesday, October 24, 2023 / 
Rules and Regulations

[[Page 73098]]


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ENVIRONMENTAL PROTECTION AGENCY

40 CFR Part 84

[EPA-HQ-OAR-2021-0643; FRL-8831-02-OAR]


Phasedown of Hydrofluorocarbons: Restrictions on the Use of 
Certain Hydrofluorocarbons Under the American Innovation and 
Manufacturing Act of 2020

AGENCY: Environmental Protection Agency (EPA).

ACTION: Final rule.

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SUMMARY: The U.S. Environmental Protection Agency is issuing 
regulations to implement certain provisions of the American Innovation 
and Manufacturing Act, as enacted on December 27, 2020. This rulemaking 
restricts the use of hydrofluorocarbons in specific sectors or 
subsectors in which they are used; establishes a process for submitting 
technology transitions petitions; establishes recordkeeping and 
reporting requirements; and addresses certain other elements related to 
the effective implementation of the American Innovation and 
Manufacturing Act. These restrictions on the use of hydrofluorocarbons 
address petitions granted on October 7, 2021, and September 19, 2022.

DATES: This rule is effective December 26, 2023.

FOR FURTHER INFORMATION CONTACT: Allison Cain, Stratospheric Protection 
Division, Office of Atmospheric Protection (Mail Code 6205A), 
Environmental Protection Agency, 1200 Pennsylvania Ave. NW, Washington, 
DC 20460; telephone number: 202-564-1566; email address: 
<a href="/cdn-cgi/l/email-protection#7714161e1959161b1b1e0418193712071659101801"><span class="__cf_email__" data-cfemail="6407050d0a4a0508080d170b0a240114054a030b12">[email&#160;protected]</span></a>. You may also visit EPA's website at <a href="https://www.epa.gov/climate-hfcs-reduction">https://www.epa.gov/climate-hfcs-reduction</a> for further information.

SUPPLEMENTARY INFORMATION: Throughout this document, whenever ``we,'' 
``us,'' ``the Agency,'' or ``our'' is used, we mean EPA. Acronyms and 
abbreviations that are used in this rulemaking that may be helpful 
include:

AC--Air Conditioning
ACIM--Automatic Commercial Ice Machine
AHAM--Association of Home Appliance Manufacturers
AHRI--Air-Conditioning, Heating, and Refrigeration Institute
AIM Act--American Innovation and Manufacturing Act of 2020
ANSI--American National Standards Institute
AR4--Fourth Assessment Report of the Intergovernmental Panel on 
Climate Change
ASHRAE--American Society of Heating, Refrigerating and Air-
Conditioning Engineers
CAA--Clean Air Act
CARB--California Air Resources Board
CBI--Confidential Business Information
CBP--U.S. Customs and Border Protection
CDR--Chemical Data Reporting
CFC--Chlorofluorocarbon
CH<INF>4</INF>--Methane
CO<INF>2</INF>--Carbon Dioxide
DOE--U.S. Department of Energy
DX--Direct Expansion
EAV--Equivalent Annualized Value
e-GGRT--Electronic Greenhouse Gas Reporting Tool
EEAP--Environmental Effects Assessment Panel
EIA--Environmental Investigation Agency
EPA--U.S. Environmental Protection Agency
EU--European Union
FDA--U.S. Food and Drug Administration
FR--Federal Register
GDP--Gross Domestic Product
GHG--Greenhouse Gas
GHGRP--Greenhouse Gas Reporting Program
GWP--Global Warming Potential
HCFC--Hydrochlorofluorocarbon
HCFO--Hydrochlorofluoroolefin
HCPA--Household and Commercial Products Association
HD--Heavy-duty
HFC--Hydrofluorocarbon
HFO--Hydrofluoroolefin
IAM--Integrated Assessment Model
IAPMO--International Association of Plumbing and Mechanical 
Officials
ICC--International Code Council
ICR--Information Collection Request
IIAR--International Institute of Ammonia Refrigeration
IPR--Industrial Process Refrigeration
IPCC--Intergovernmental Panel on Climate Change
IT--Information Technology
ITEF--Information Technology Equipment Facilities
IWG--Interagency Working Group on the Social Cost of Greenhouse 
Gases
LD--Light-duty
LFL--Lower Flammability Limit
MAC--Marginal Abatement Cost
MDPV--Medium-duty Passenger Vehicle
MMTCO<INF>2</INF>e--Million Metric Tons of Carbon Dioxide Equivalent
MMTEVe--Million Metric Tons of Exchange Value Equivalent
MVAC--Motor Vehicle Air Conditioning
MY--Model Year
N<INF>2</INF>O--Nitrous oxide
NAICS--North American Industry Classification System
NAMA--National Automatic Merchandising Association
NATA--National Air Toxics Assessment
NFPA--National Fire Protection Association
NRDC--Natural Resources Defense Council
NRTL--Nationally Recognized Testing Laboratory
OEM--Original Equipment Manufacturer
ODS--Ozone-depleting Substance
OMB--U.S. Office of Management and Budget
OSHA--Occupational Safety and Health Administration
PFAS--Per- and Polyfluoroalkyl Substances
PFC--Perfluorocarbon
PRA--Paperwork Reduction Act
PTAC--Packaged Terminal Air Conditioner
PTHP--Packaged Terminal Heat Pump
PV--Present Value
RACHP--Refrigeration, Air Conditioning, and Heat Pumps
RFA--Regulatory Flexibility Act
RIA--Regulatory Impact Analysis
RTOC--Refrigeration, Air Conditioning and Heat Pumps Technical 
Options Committee
SBREFA--Small Business Regulatory Enforcement Fairness Act
SC-GHG--Social Cost of GHGs
SC-HFCs--Social Costs of Hydrofluorocarbons
SF<INF>6</INF>--Sulfur Hexafluoride
SMRE--Semiconductor Manufacturing and Related Equipment
SNAP--Significant New Alternatives Policy
TEAP--Technology and Economic Assessment Panel
TFA--Trifluoroacetic Acid
TLV-TWA--Threshold Limit Value-Time-Weighted Average
TOC--Technical Options Committee
TRI--Toxics Release Inventory
TSD--Technical Support Document
UL--Underwriters Laboratories Inc
VOCs--Volatile Organic Compounds
VRF--Variable Refrigerant Flow
WMO--World Meteorological Organization

Table of Contents

I. Executive Summary
    A. What is the purpose of this regulatory action?
    B. What is the summary of this regulatory action?
    C. What is the summary of the costs and benefits of this action?
II. General Information
    A. Does this action apply to me?
    B. What is EPA's authority for taking this action?
III. Background
    A. What are HFCs?
    B. How do HFCs affect public health and welfare?
IV. What is the petition process under the technology transitions 
program?
    A. What must be included in a technology transitions petition?
    B. What happens after a petition is submitted?
    C. Can I revise or resubmit my petition?
V. How is EPA considering negotiated rulemaking?
    A. Summary of the AIM Act's Directive on Negotiated Rulemaking
    B. How does EPA intend to consider negotiating with stakeholders 
under the AIM Act?
VI. How is EPA restricting the use of HFCs?
    A. What definitions is EPA establishing in subsection (i)?
    B. How is EPA restricting the use of HFCs in the sector or 
subsector in which they are used?
    C. Applicability
    1. What is EPA's statutory authority for this action?
    2. What uses is EPA restricting in this rule?
    3. What uses are not covered in the final rule?

[[Page 73099]]

    D. How is EPA addressing restrictions on the use of HFCs 
requested in petitions granted?
    1. Petitions Granted on October 7, 2021
    2. How is EPA addressing additional petitions that cover similar 
sectors and subsectors?
    3. Petitions Granted on September 19, 2022
    E. Subsection (i)(4) Factors for Determination
    1. How is EPA considering best available data?
    2. How is EPA considering the availability of substitutes?
    3. How is EPA considering overall economic costs and 
environmental impacts, as compared to historical trends?
    4. How is EPA considering the remaining phasedown period for 
regulated substances?
    5. How did EPA determine the degree of the restrictions for each 
sector and subsector?
    F. For which sectors and subsectors is EPA establishing 
restrictions on the use of HFCs?
    1. Refrigeration, Air Conditioning, and Heat Pumps
    2. Foams
    3. Aerosols
VII. What are the labeling requirements?
VIII. What are the reporting and recordkeeping requirements?
    A. What reporting is EPA requiring?
    1. What is the frequency and timing of reporting?
    2. When do reporters need to begin reporting?
    B. What recordkeeping is EPA requiring?
IX. What are the costs and benefits of this action?
    A. Assessment of Costs and Additional Benefits Utilizing 
Transition Options
    B. Scoping Analysis of Imports of Products
X. How is EPA evaluating environmental justice?
XI. Judicial Review
XII. Severability
XIII. Statutory and Executive Order Review
    A. Executive Order 12866: Regulatory Planning and Review and 
Executive Order 14094: Modernizing Regulatory Review
    B. Paperwork Reduction Act (PRA)
    C. Regulatory Flexibility Act (RFA)
    D. Unfunded Mandates Reform Act (UMRA)
    E. Executive Order 13132: Federalism
    F. Executive Order 13175: Consultation and Coordination With 
Indian Tribal Governments
    G. Executive Order 13045: Protection of Children From 
Environmental Health Risks and Safety Risks
    H. Executive Order 13211: Actions That Significantly Affect 
Energy Supply, Distribution, or Use
    I. National Technology Transfer and Advancement Act (NTTAA) and 
Incorporation by Reference
    J. Executive Order 12898: Federal Actions To Address 
Environmental Justice in Minority Populations and Low-Income 
Populations and Executive Order 14096: Revitalizing our Nation's 
Commitment to Environmental Justice for All
    K. Congressional Review Act (CRA)

I. Executive Summary

A. What is the purpose of this regulatory action?

    The U.S. Environmental Protection Agency (EPA) is issuing 
regulations to implement certain provisions of the American Innovation 
and Manufacturing Act of 2020, codified at 42 U.S.C. 7675 (AIM Act or 
the Act). The AIM Act authorizes EPA to address hydrofluorocarbons 
(HFCs) in three main ways: phasing down HFC production and consumption 
through an allowance allocation program; \1\ promulgating certain 
regulations for purposes of maximizing reclamation and minimizing 
releases of HFCs from equipment; and facilitating sector-based 
transitions to next-generation technologies. This rulemaking focuses on 
the third area--facilitating the transition to next-generation 
technologies by restricting use of HFCs in the sectors or subsectors in 
which they are used.
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    \1\ EPA has issued regulations establishing and codifying a 
framework for phasing down HFC production and consumption through an 
allowance allocation program, ``Phasedown of Hydrofluorocarbons: 
Establishing the Allowance Allocation and Trading Program Under the 
American Innovation and Manufacturing Act'' (86 FR 55116, October 5, 
2021). That rule is referred to as the ``Allocation Framework Rule'' 
throughout this document. EPA finalized a separate rulemaking to 
update certain aspects of that regulatory framework (see final rule 
at 88 FR 46836, July 20, 2023).
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    Subsection (i) of the Act, entitled ``Technology Transitions,'' 
authorizes EPA, by rulemaking, to restrict the use of regulated 
substances (used interchangeably with ``HFCs'' in this document) in 
sectors or subsectors where the regulated substances are used.\2\ The 
Act also includes provisions for the public to petition EPA to initiate 
such a rulemaking. On October 7, 2021, and September 19, 2022, EPA 
granted 12 petitions and partially granted one petition (hereby 
referred to as ``granted petitions'') requesting restrictions on the 
use of HFCs in various sectors and subsectors (86 FR 57141, October 14, 
2021). The Act directs EPA to promulgate a final rule within two years 
after the date on which the Agency grants a petition. This rulemaking, 
in part, addresses the granted petitions.
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    \2\ The Act lists 18 saturated HFCs, and by reference any of 
their isomers not so listed, that are covered by the statute's 
provisions, referred to as ``regulated substances'' under the Act.
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    This rulemaking further addresses the framework for how EPA intends 
to implement its authority to restrict the use of HFCs in sectors and 
subsectors where they are used. It includes provisions to support 
implementation of, compliance with, and enforcement of statutory and 
regulatory requirements under subsection (i) of the Act. To provide the 
public with additional information about this new program, this 
document also includes a description of how EPA intends to implement 
certain aspects of the program, such as the processing of petitions to 
restrict the use of HFCs in sectors and subsectors in which they are 
used under subsection (i) of the Act.

B. What is the summary of this regulatory action?

    EPA is establishing the process and information requirements for 
submitting petitions under subsection (i) of the AIM Act and describing 
how the Agency intends to evaluate those petitions. Upon receiving a 
petition, the Agency will consider, to the extent practicable, the 
factors listed in subsection (i)(4) of the AIM Act in making a 
determination to grant or deny the petition. Consistent with the Act, 
EPA considered these factors to the extent practicable in establishing 
the restrictions on the use of HFCs in this rulemaking.
    EPA is restricting the use of HFCs, whether neat or used in a 
blend, with high global warming potentials (GWPs) within the 
refrigeration, air conditioning, and heat pump (RACHP), foam, and 
aerosol sectors. EPA is prohibiting the manufacture, import, or 
installation of certain equipment across approximately 40 subsectors, 
either based on overall GWP limits or restrictions on use of specific 
HFCs. The compliance dates for these restrictions vary depending on the 
subsector ranging from January 1, 2025, to January 1, 2028. The final 
rule prohibits the sale, distribution, and export of factory completed 
products that do not comply with the relevant restrictions three years 
after the prohibition on manufacture and import. EPA is not regulating 
at this time actions with respect to components needed to service or 
repair existing systems. EPA is finalizing labeling, annual reporting, 
and recordkeeping requirements for products and specified components 
that are imported or domestically manufactured that use or are intended 
to use an HFC.

C. What is the summary of the costs and benefits of this action?

    EPA is providing a summary of the costs and benefits of restricting 
use of HFCs consistent with this rule. The full analyses, presented in 
the American Innovation and Manufacturing Act of 2020--Subsection 
(i)(4) Factors for Determination: Costs and Environmental Impacts, 
referred to in

[[Page 73100]]

this preamble as the Costs and Environmental Impacts technical support 
document (TSD) and in a regulatory impact analysis (RIA) addendum to 
the Allocation Framework RIA, are contained in the docket to this rule. 
These analyses--as summarized below--highlight economic costs and 
benefits, including benefits from HFC consumption and emission 
reductions.
    EPA relied on previous analyses conducted for the Allocation 
Framework Rule (86 FR 55116, October 5, 2021) and the 2024 Allocation 
Rule, ``Phasedown of Hydrofluorocarbons: Allowance Allocation 
Methodology for 2024 and Later Years'' (88 FR 46836, July 20, 2023), as 
a starting point for the assessment of costs and benefits of this rule. 
In this way, EPA analyzed the incremental impacts of this rule, 
attributing benefits only insofar as they are additional to those 
already assessed in the Allocation Framework RIA and 2024 Allocation 
Rule RIA addendum (collectively referred to as ``Allocation Rules'' in 
this discussion.\3\
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    \3\ In a separate action, EPA has also issued a rule to amend 
the production baseline downwards by 0.005% to reflect corrected 
data (88 FR 44220, July 12, 2023).
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    The additional benefits of this rule relative to the Allocation 
Rules may vary depending on the mix and timing of industry transitions 
made to achieve compliance in affected subsectors. In its analysis of 
the Allocation Rules, EPA estimated that regulated entities would adopt 
specific technology transition options to achieve compliance with the 
statutory allowance cap step-downs. Industry is already making many of 
these transitions, and we expect that achieving the allowance cap step-
downs will require many of the same subsector-specific technology 
transitions that are also required by this rule. However, this rule may 
in some cases require regulated entities to further accelerate 
transitions in specific subsectors, relative to what EPA previously 
assumed in its analysis of the Allocation Rules. Conversely, entities 
in a discrete set of subsectors not covered by this rule could 
conceivably forgo or delay adopting abatement options that were assumed 
to be undertaken to comply with the Allocation Rules.
    Given this uncertainty, EPA analyzed two scenarios to represent the 
range of potential incremental impacts resulting from this rule: a 
``base case'' and ``high additionality case.'' Both scenarios use the 
results from the Allocation Framework Rule as a starting point and 
count benefits in terms of reductions of consumption and emissions only 
in cases where this rule results in additional reductions in HFC 
consumption. The ``base case'' represents a conservative assessment of 
benefits and assumes that any industry activity not necessary for 
compliance is excluded. In other words, the scenario excludes 
consumption reductions not covered by a GWP restriction in this rule. 
By contrast, the ``high additionality case'' is a less conservative 
scenario and assumes that HFC consumption reduction activities not 
covered by this rule would remain consistent with the Allocation 
Framework Rule reference scenario (i.e., neither increase nor decrease 
in response to this rule). Based on the results of these two scenarios, 
which are detailed further in the Costs and Environmental Impacts TSD 
and the RIA addendum, EPA estimates that additional emission reductions 
through 2050 would range from an annual average of 3 to 34 million 
metric tons of carbon dioxide equivalent (MMTCO<INF>2</INF>e) \4\ in 
the base case and high additionality case, respectively. These emission 
reductions generally lag the anticipated incremental consumption 
reductions, which range from an annual average of 28 to 43 
MMTCO<INF>2</INF>e.
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    \4\ The exchange values provided in the AIM Act are numerically 
equivalent to the 100-year integrated global warming potentials 
provided in IPCC (2007). EPA provides values in CO<INF>2</INF>e and 
notes that the same values would be used if expressed in exchange 
value equivalents.
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    Table 1 summarizes the reductions in both consumption and emissions 
as described in the Costs and Environmental Impacts TSD and the RIA 
addendum for this final rule. The table shows the cumulative 
incremental reductions--that is, the difference in reductions compared 
with the Allocation Framework Rule reference scenario--from the final 
rule over the time period 2025 through 2050. Both the base case and 
high additionality case results show a net reduction in consumption and 
emissions on a cumulative basis through 2050.

 Table 1--Incremental Consumption and Emission Reductions in the Technology Transitions Rule Base Case and High
                        Additionality Case Compared to the Allocation Rule Reference Case
----------------------------------------------------------------------------------------------------------------
Cumulative incremental consumption reductions (MMTCO2e)-- Cumulative incremental emission reductions (MMTCO2e)--
                        2025-2050                                                2025-2050
----------------------------------------------------------------------------------------------------------------
Technology transitions rule  Technology transitions high    Technology transitions      Technology transitions
         base case                additionality case            rule base case          high additionality case
----------------------------------------------------------------------------------------------------------------
                    720                        1,113                           83                         876
----------------------------------------------------------------------------------------------------------------

    Although the base case is a reasonable projection of the potential 
impacts of this rule, there is reason to believe that it is a 
conservative one, and that the incremental emission reductions 
associated with this final rule could be far greater than reflected in 
the base case scenario. Previous regulatory programs to reduce chemical 
use in the affected industries show that regulated entities do not 
limit their response to the required compliance level; rather, 
regulated entities may take additional actions that transform industry 
practices for various reasons, including the anticipation of future 
restrictions, strengthening their competitive position, and supporting 
overall environmental goals. For example, U.S. production and 
consumption of ozone-depleting substances (ODS) during their phaseout 
was consistently below the limits established under the Montreal 
Protocol. For this reason, the high additionality case assumes certain 
abatement options not covered by the final rule--but which were assumed 
in the prior accounting of benefits for the Allocation Rules--continue 
to be undertaken. Based on the two scenarios, on a cumulative basis 
this rule is expected to yield incremental emission reductions ranging 
from 83 to 876 MMTCO<INF>2</INF>e through 2050 (respectively, about 2 
percent and 20 percent of the total emission reductions over that same 
time period in the Allocation Rules analyses). In the RIA addendum, we 
estimate the present value of these

[[Page 73101]]

incremental benefits to be between $3.01 billion and $50.4 billion in 
2020 dollars.
    EPA also estimates that this rule will result in potentially lower 
compliance costs relative to those previously assessed for the 
Allocation Rules. These additional savings stem largely from assumed 
energy efficiency gains and lower cost refrigerants associated with the 
technological transitions necessary to meet the requirements.\5\ The 
present value of cumulative incremental costs or savings from 2025-2050 
is estimated to be between $1 million in costs and $2.1 billion in 
savings, when using a 7 percent discount rate, or between $1.6 billion 
and $4.5 billion in savings, when using a 3 percent discount rate (in 
2020 dollars). As with EPA's estimates of benefits for this rule, these 
estimated costs or savings reflect only what is incremental to EPA's 
previously estimated compliance pathway for the Allocation Rules.\6\
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    \5\ As discussed in the RIA Addendum, incremental savings 
estimated for this rule stem largely from more rapid and more 
comprehensive transitions to cost-saving, lower-GWP technologies in 
certain subsectors than was previously estimated for the HFC 
Allocation Framework Rule. Similarly comprehensive transitions were 
not assumed in the Allocation Rules analysis, since it assumed 
that--absent regulatory requirements--newer technologies may still 
face some industry inertia and shift less rapidly regardless of 
potential energy savings or other benefits over time.
    \6\ In the 2024 Allocation Rule RIA Addendum, EPA estimated 
present value net savings for the period of 2022-2050 of $9 billion 
discounted at 3 percent and $4.8 billion at 7 percent, in 2020 
dollars, discounted to 2022. Estimated net savings for the TT Rule 
are incremental to these prior estimates.
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    Table 2 summarizes key findings from the RIA addendum, including 
the present value (PV) and equivalent annualized value (EAV) of 
cumulative incremental climate benefits, costs, and net benefits of 
this rule over the 2025-2050 time period. Climate benefits are 
discounted at 3 percent, and costs are presented using both a 3 percent 
and 7 percent discount rate. The climate benefits and net benefits 
findings were not used for decisional purposes and are provided for 
informational and illustrative purposes only.

                      Table 2--PV and EAV of Cumulative Incremental Climate Benefits, Costs, and Net Benefits for 2025 Through 2050
                                                     [Millions of 2020$, discounted to 2022] a b c d
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                               Base case                                         High additionality case
                                       -----------------------------------------------------------------------------------------------------------------
                                        Incremental      Annual costs        Net benefits (3%    Incremental      Annual costs        Net benefits (3%
                                          climate    (negative values are   benefits, 3% or 7%     climate    (negative values are   benefits, 3% or 7%
             Discount rate                benefits         savings)             costs) \e\         benefits         savings)             costs) \e\
                                            (3%)    --------------------------------------------     (3%)    -------------------------------------------
                                       -------------                                            -------------
                                             3%          3%         7%         3%         7%          3%          3%         7%         3%         7%
--------------------------------------------------------------------------------------------------------------------------------------------------------
PV....................................       $3,013   ($4,549)   ($2,073)     $7,561     $5,086      $50,406   ($1,601)         $1    $52,007    $50,405
EAV...................................          184      (278)      (215)        462        399        3,081       (98)          0      3,179      3,081
--------------------------------------------------------------------------------------------------------------------------------------------------------
\a\ Benefits include only those related to climate. Climate benefits are based on changes in HFC emissions and are calculated using four different
  estimates of the SC-HFCs (model average at 2.5 percent, 3 percent, and 5 percent discount rates; 95th percentile at 3 percent discount rate). For
  purposes of this table, we show the effects associated with the model average at a 3 percent discount rate, but the Agency does not have a single
  central SC-HFC point estimate. We emphasize the importance and value of considering the benefits calculated using all four SC-HFC estimates. As
  discussed in Chapter 5 of the RIA addendum a consideration of climate effects calculated using discount rates below 3 percent, including 2 percent and
  lower, is also warranted when discounting intergenerational impacts.
\b\ Rows may not appear to add correctly due to rounding.
\c\ The annualized present value of costs and benefits are calculated as if they occur over a 26-year period from 2025 to 2050.
\d\ The PV for the 7% net benefits column is found by taking the difference between the PV of climate benefits at 3% and the PV of costs discounted at
  7%. Due to the intergenerational nature of climate impacts the social rate of return to capital, estimated to be 7 percent in Office of Management and
  Budget's Circular A-4, is not appropriate for use in calculating PV of climate benefits.

    Some of the information regarding projected impacts of this rule, 
including cost estimates and anticipated environmental impacts, was 
considered by EPA in its assessment of certain factors listed in 
subsection (i)(4) of the AIM Act.\7\ The cost and benefit information 
relied upon by EPA in its consideration of the subsection (i)(4) 
factors is compiled in the Costs and Environmental Impacts TSD. As 
discussed in section VI.E, EPA chose to use certain cost and 
environmental benefit information that it had generated in conducting 
its RIA addendum in considering certain factors under subsection 
(i)(4), but we expect that in future rulemakings we may consider 
different types of information to address the (i)(4) factors. In 
assessing the (i)(4) factors for this rule, as summarized in the Costs 
and Environmental Impacts TSD, EPA considered estimates of costs of the 
action, without incorporating the social costs of HFCs (SC-HFCs), and 
estimates of cumulative consumption and emission reductions for 2025-
2050 of 720 to 1,113 MMTCO<INF>2</INF>e and 83 to 876 
MMTCO<INF>2</INF>e, respectively. The analysis demonstrates net 
positive incremental environmental impacts (i.e., HFC consumption and 
emission reductions) and cost savings relative to the compliance 
pathway evaluated for the Allocation Rules. However, there was no 
specific quantitative threshold for positive incremental impacts used 
to evaluate the subsection (i)(4) factors. Rather, in its review, to 
the extent practicable, of the overall economic costs and environmental 
impacts, as compared to historical trends, the Agency issued the final 
restrictions after considering the general findings that: a) there are 
in fact positive incremental impacts expected from this rule, and b) 
that the overall impact of the regulations implemented under the AIM 
Act to date (including both the Allocation Rules and this rule) remains 
net positive in terms of overall costs and environmental impacts.\8\
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    \7\ Subsection (i)(4) of the AIM Act contains a list of factors 
that the statute directs EPA to consider, to the extent practicable, 
when carrying out a rulemaking or making a determination to grant or 
deny a petition.
    \8\ We note, however, that subsection (i)(4)(C) plainly does not 
require a finding that the environmental impacts of a rule exceed 
the economic costs.
---------------------------------------------------------------------------

    Although EPA is using SC-HFCs for purposes of some of the analysis 
in the RIA addendum, this action does not rely on those estimates of 
these costs as a record basis for the Agency action, and EPA would 
reach this rule's conclusions even in the absence of the social costs 
of HFCs.
    Additional information on this analysis can be found in section IX 
of this preamble and in the Costs and Environmental Impacts TSD and RIA 
addendum contained in the docket.

[[Page 73102]]

II. General Information

A. Does this action apply to me?

    You may be potentially affected by this rule if you manufacture, 
import, export, sell, distribute, or install equipment that uses or is 
intended to use HFCs, such as refrigeration and air-conditioning 
systems, foams, and aerosols. Potentially affected categories, by North 
American Industry Classification System (NAICS) code, are included in 
Table 3.

     Table 3--NAICS Classification of Potentially Affected Entities
------------------------------------------------------------------------
        NAICS code                   NAICS industry description
------------------------------------------------------------------------
238220...................  Plumbing, Heating, and Air Conditioning
                            Contractors.
311812...................  Commercial Bakeries.
321999...................  All Other Miscellaneous Wood Product
                            Manufacturing.
322299...................  All Other Converted Paper Product
                            Manufacturing.
324191...................  Petroleum Lubricating Oil and Grease
                            Manufacturing.
324199...................  All Other Petroleum and Coal Products
                            Manufacturing.
325199...................  All Other Basic Organic Chemical
                            Manufacturing.
325211...................  Plastics Material and Resin Manufacturing.
325412...................  Pharmaceutical Preparation Manufacturing.
325414...................  Biological Product (except Diagnostic)
                            Manufacturing.
325998...................  All Other Miscellaneous Chemical Product and
                            Preparation Manufacturing.
326150...................  Urethane and Other Foam Product.
326299...................  All Other Rubber Product Manufacturing.
327999...................  All Other Miscellaneous Nonmetallic Mineral
                            Product Manufacturing.
332812...................  Metal Coating, Engraving (except Jewelry and
                            Silverware), and Allied Services to
                            Manufacturers.
332999...................  All Other Miscellaneous Fabricated Metal
                            Product Manufacturing.
333415...................  Air[dash]Conditioning and Warm Air Heating
                            Equipment and Commercial and Industrial
                            Refrigeration Equipment Manufacturing.
333511...................  Industrial Mold Manufacturing.
333912...................  Air and Gas Compressor Manufacturing.
333999...................  All Other Miscellaneous General Purpose
                            Machinery Manufacturing.
334419...................  Other Electronic Component Manufacturing.
335220...................  Major Household Appliance Manufacturing.
336120...................  Heavy Duty Truck Manufacturing.
336212...................  Truck Trailer Manufacturing.
336214...................  Travel Trailer and Camper Manufacturing.
3363.....................  Motor Vehicle Parts Manufacturing.
3364.....................  Aerospace Product and Parts Manufacturing.
336411...................  Aircraft Manufacturing.
336611...................  Ship Building and Repairing.
336612...................  Boat Building.
336992...................  Military Armored Vehicle, Tank, and Tank
                            Component Manufacturing.
337214...................  Office Furniture (Except Wood) Manufacturing.
339112...................  Surgical and Medical Instrument
                            Manufacturing.
339113...................  Surgical Appliance and Supplies
                            Manufacturing.
339999...................  All Other Miscellaneous Manufacturing.
423120...................  Motor Vehicle Supplies and New Parts Merchant
                            Wholesalers.
423450...................  Medical, Dental, and Hospital Equipment and
                            Supplies Merchant Wholesalers.
423610...................  Electrical Apparatus and Equipment, Wiring
                            Supplies, and Related Equipment Merchant
                            Wholesalers.
423620...................  Household Appliances, Electric Housewares,
                            and Consumer Electronics Merchant
                            Wholesalers.
423690...................  Other Electronic Parts and Equipment Merchant
                            Wholesalers.
423720...................  Plumbing and Heating Equipment and Supplies
                            (Hydronics) Merchant Wholesalers.
423730...................  Warm Air Heating and Air[dash]Conditioning
                            Equipment and Supplies Merchant Wholesalers.
423740...................  Refrigeration Equipment and Supplies Merchant
                            Wholesalers.
423830...................  Industrial Machinery and Equipment Merchant
                            Wholesalers.
423840...................  Industrial Supplies Merchant Wholesalers.
423850...................  Service Establishment Equipment and Supplies
                            Merchant Wholesalers.
423860...................  Transportation Equipment and Supplies (except
                            Motor Vehicle) Merchant Wholesalers.
423990...................  Other Miscellaneous Durable Goods Merchant
                            Wholesalers.
424690...................  Other Chemical and Allied Products Merchant
                            Wholesalers.
424820...................  Wine and Distilled Alcoholic Beverage
                            Merchant Wholesalers.
443142...................  Electronics Stores.
444190...................  Other Building Material Dealers.
445110...................  Supermarkets and Other Grocery (except
                            Convenience) Stores.
445131...................  Convenience Retailers.
445298...................  All Other Specialty Food Retailers.
449210...................  Appliance Stores, Household-Type.
453998...................  All Other Miscellaneous Store Retailers
                            (except Tobacco Stores).
45711....................  Gasoline Stations With Convenience Stores.
481111...................  Scheduled Passenger Air Transportation.
531120...................  Lessors of Nonresidential Buildings (except
                            Miniwarehouses).
541330...................  Engineering Services.
541380...................  Testing Laboratories.
541512...................  Computer Systems Design Services.
541519...................  Other Computer Related Services.
541620...................  Environmental Consulting Services.
562111...................  Solid Waste Collection.

[[Page 73103]]

 
562211...................  Hazardous Waste Treatment and Disposal.
562920...................  Materials Recovery Facilities.
621498...................  All Other Outpatient Care Centers.
621999...................  All Other Miscellaneous Ambulatory Health
                            Care Services.
72111....................  Hotels (Except Casino Hotels) and Motels.
72112....................  Casino Hotels.
72241....................  Drinking Places (Alcoholic Beverages).
722513...................  Limited-Service Restaurants.
722514...................  Cafeterias, Grill Buffets, and Buffets.
722515...................  Snack and Nonalcoholic Beverage Bars.
81119....................  Other Automotive Repair and Maintenance.
811219...................  Other Electronic and Precision Equipment
                            Repair and Maintenance.
811412...................  Appliance Repair and Maintenance.
922160...................  Fire Protection.
------------------------------------------------------------------------

    Table 3 is not intended to be exhaustive, but rather provides a 
guide for readers regarding entities likely to be regulated by this 
action. This table lists the types of entities that EPA expects could 
potentially be regulated by this action. Other types of entities not 
listed in the table could also be regulated. To determine whether your 
entity may be regulated by this action, you should carefully examine 
the regulatory text at the end of this document. If you have questions 
regarding the applicability of this action to a particular entity, 
consult the person listed in the FOR FURTHER INFORMATION CONTACT 
section.

B. What is EPA's authority for taking this action?

    On December 27, 2020, the AIM Act was enacted as section 103 in 
Division S, Innovation for the Environment, of the Consolidated 
Appropriations Act, 2021 (codified at 42 U.S.C. 7675). Subsection 
(k)(1)(C) of the Act provides that Clean Air Act (CAA) sections 113, 
114, 304, and 307 apply to the AIM Act and any regulations EPA 
promulgates under the AIM Act as though the AIM Act were part of title 
VI of the CAA. Accordingly, this rulemaking is subject to CAA section 
307(d) (see 42 U.S.C. 7607(d)(1)(I)) (CAA section 307(d) applies to 
``promulgation or revision of regulations under subchapter VI of this 
chapter (relating to stratosphere and ozone protection)'').
    The AIM Act authorizes EPA to address HFCs by providing new 
authorities in three main areas: phasing down the production and 
consumption of listed HFCs; managing these HFCs and their substitutes; 
and facilitating the transition to next-generation technologies by 
restricting use of these HFCs in the sector or subsectors in which they 
are used. This rulemaking focuses on the third area: the transition to 
next-generation technologies by restricting use of these HFCs in the 
sector or subsectors in which they are used.
    In subsection (k)(1)(A), the AIM Act provides EPA with the 
authority to promulgate necessary regulations to carry out EPA's 
functions under the Act, including its obligations to ensure that the 
Act's requirements are satisfied. Subsection (i) of the AIM Act, 
``Technology Transitions,'' provides that ``the Administrator may by 
rule restrict, fully, partially, or on a graduated schedule, the use of 
a regulated substance in the sector or subsector in which the regulated 
substance is used.'' 42 U.S.C. 7675(i)(1). The Act lists 18 saturated 
HFCs, and by reference any of their isomers not so listed, that are 
covered by the statute's provisions, referred to as ``regulated 
substances'' under the Act.\9\ (42 U.S.C. 7675(c)(1)). EPA is also 
authorized to designate additional substances that meet certain 
criteria as regulated substances (42 U.S.C. 7675(c)(3)). EPA has not so 
designated any additional substances, and the list of 18 regulated 
substances can also be found in appendix A of 40 CFR part 84. Through 
this rule, EPA is restricting the use of certain HFCs, whether neat or 
used in a blend, in specific sectors or subsectors, based on EPA's 
consideration of the factors listed in subsection (i)(4) of the AIM 
Act.
---------------------------------------------------------------------------

    \9\ As noted previously in this document, ``regulated 
substance'' and ``HFC'' are used interchangeably in this document.
---------------------------------------------------------------------------

    A rulemaking restricting the use of regulated substances in sectors 
or subsectors can be initiated by EPA on its own accord, or a person 
may petition EPA to promulgate such a rule. Specifically, subsection 
(i)(3)(A) states, ``A person may petition the Administrator to 
promulgate a rule under [subsection (i)(1)] for the restriction on use 
of a regulated substance in a sector or subsector.'' Where the Agency 
grants such a petition submitted under subsection (i), the statute 
requires that ``the Administrator shall promulgate a final rule not 
later than 2 years after the date on which the Administrator grants the 
petition.'' (42 U.S.C. 7675(i)(3)(C)(ii)). This rule addresses the 
granted petitions under subsection (i).
    Furthermore, prior to proposing a rule, subsection (i)(2)(A) 
directs EPA to consider negotiating with stakeholders in the sector or 
subsector subject to the potential rule in accordance with negotiated 
rulemaking procedures established under subchapter III of chapter 5 of 
title 5, United States Code (5 U.S.C. 563, commonly known as the 
``Negotiated Rulemaking Act of 1990''). A brief discussion on EPA's 
consideration of using negotiated rulemaking procedures and its 
decision not to use such procedures prior to proposal can be found in 
section VI.B of the proposed rule (87 FR 76775; December 15, 2022, 
hereafter ``proposed rule'').
    EPA is also finalizing measures designed to assist with enforcement 
and to help ensure compliance with the HFC use restrictions, including 
recordkeeping, reporting, and labeling requirements. Reporting is also 
necessary to inform EPA of the transitions that are occurring in those 
sectors and subsectors addressed by this rule. EPA notes that 
subsection (k)(1)(C) of the AIM Act states that section 114 of the CAA 
applies to the AIM Act and rules promulgated under it as if the AIM Act 
were included in title VI of the CAA. Thus, section 114 of the CAA, 
which provides authority to the EPA Administrator to require 
recordkeeping and reporting in carrying out provisions of the CAA, also 
applies to and supports this rulemaking.
    Subsection (i)(6) of the AIM Act states that ``[n]o rule under this 
subsection may take effect before the date that is 1 year after the 
date on which the

[[Page 73104]]

Administrator promulgates the applicable rule under this subsection.'' 
EPA interprets this provision as applying to the establishment of 
restrictions on use of HFCs under subsection (i)(1) of the Act. 
Therefore, EPA is establishing compliance dates for the restrictions on 
the manufacture and import of products and installation of systems that 
are at least one year from the date this rule is promulgated, in 
accordance with this statutory provision.
    The provisions pertaining to program administration and petitions 
processing (i.e., Sec.  84.62) do not include a delayed compliance 
date, and those provisions will come into effect 60 days after 
publication of the final rule in the Federal Register. This approach is 
based on an interpretation that subsection (i)(6) does not apply to 
those administrative provisions because ``applicable rules'' in (i)(6) 
are limited to rules that apply use restrictions under (i)(1). As a 
practical matter, the regulated industry to which a use restriction 
rule is being applied may need a full year to come into compliance with 
that restriction. While a petitioner may need some amount of time to 
collect the information needed in a petition, 60 days is a reasonable 
timeframe in which to do so. EPA did not receive comments on this 
approach.

III. Background

A. What are HFCs?

    HFCs are anthropogenic \10\ fluorinated chemicals that have no 
known natural sources. HFCs are used in a variety of applications such 
as refrigeration and air conditioning, foam blowing agents, solvents, 
aerosols, and fire suppression. HFCs are potent greenhouse gases (GHGs) 
with 100-year GWPs (a measure of the relative climatic impact of a GHG) 
that can be hundreds to thousands of times that of carbon dioxide 
(CO<INF>2</INF>).
---------------------------------------------------------------------------

    \10\ While the overwhelming majority of HFC production is 
intentional, EPA is aware that HFC-23 can be a byproduct associated 
with the production of other chemicals, including but not limited to 
hydrochlorofluorocarbon (HCFC)-22 and other fluorinated gases.
---------------------------------------------------------------------------

    HFC use and emissions have been growing worldwide due to the global 
phaseout of ODS under the Montreal Protocol and the increasing use of 
refrigeration and air-conditioning equipment globally.\11\ HFC 
emissions had previously been projected to increase substantially over 
the next several decades. In 2016, in Kigali, Rwanda, countries agreed 
to adopt an amendment to the Montreal Protocol, known as the Kigali 
Amendment, which provides for a global phasedown of the production and 
consumption of HFCs. The United States ratified the Kigali Amendment on 
October 31, 2022. Global adherence to the Kigali Amendment would 
substantially reduce future emissions, leading to a peaking of HFC 
emissions before 2040.<SUP>12 13</SUP>
---------------------------------------------------------------------------

    \11\ World Meteorological Organization (WMO), Scientific 
Assessment of Ozone Depletion: 2022, GAW Report No. 278, 509 pp., 
WMO, Geneva, Switzerland, 2022. Available at: <a href="https://ozone.unep.org/system/files/documents/Scientific-Assessment-of-Ozone-Depletion-2022.pdf">https://ozone.unep.org/system/files/documents/Scientific-Assessment-of-Ozone-Depletion-2022.pdf</a>.
    \12\ Ibid.
    \13\ A recent study estimated that global compliance with the 
Kigali Amendment is expected to lower 2050 annual emissions by 3.0-
4.4 million metric tons of carbon dioxide equivalent 
(MMTCO<INF>2</INF>e). Guus J.M. Velders et al. Projections of 
hydrofluorocarbon (HFC) emissions and the resulting global warming 
based on recent trends in observed abundances and current policies. 
Atmos. Chem. Phys., 22, 6087-6101, 2022. Available at: <a href="https://doi.org/10.5194/acp-22-6087-2022">https://doi.org/10.5194/acp-22-6087-2022</a>.
---------------------------------------------------------------------------

    Atmospheric observations of most currently measured HFCs confirm 
their abundances are increasing at accelerating rates. Total emissions 
of HFCs increased by 23 percent from 2012 to 2016 \14\ and a further 19 
percent from 2016 to 2020.\15\ The four most abundant HFCs in the 
atmosphere, in GWP-weighted terms, are HFC-134a, HFC-125, HFC-23, and 
HFC-143a.\16\
---------------------------------------------------------------------------

    \14\ World Meteorological Organization (WMO), Scientific 
Assessment of Ozone Depletion: 2018, World Meteorological 
Organization, Global Ozone Research and Monitoring Project--Report 
No. 58, 588 pp., Geneva, Switzerland, 2018. Available at: <a href="https://ozone.unep.org/sites/default/files/2019-05/SAP-2018-Assessment-report.pdf">https://ozone.unep.org/sites/default/files/2019-05/SAP-2018-Assessment-report.pdf</a>.
    \15\ WMO, 2022.
    \16\ Ibid.
---------------------------------------------------------------------------

    HFCs excluding HFC-23 accounted for a radiative forcing of 0.025 W/
m\2\ in 2016 rising to 0.037 W/m\2\ in 2020. This radiative forcing was 
projected to increase by an order of magnitude to 0.25 W/m\2\ by 2050. 
If the Kigali Amendment were to be fully implemented, it would be 
expected to reduce the future radiative forcing due to HFCs (excluding 
HFC-23) to 0.13 W/m\2\ in 2050 which is a reduction of about 50 percent 
compared with the radiative forcing projected in the business-as-usual 
scenario of uncontrolled HFCs.\17\
---------------------------------------------------------------------------

    \17\ Velders, 2022.
---------------------------------------------------------------------------

    There are hundreds of possible HFC compounds. The 18 HFCs listed as 
regulated substances by the AIM Act are some of the most commonly used 
HFCs (neat and in blends) and have high impacts as measured by the 
quantity of each substance emitted multiplied by their respective 
GWPs.\18\ These 18 HFCs are all saturated, meaning they have only 
single bonds between their atoms and therefore have longer atmospheric 
lifetimes.
---------------------------------------------------------------------------

    \18\ The AIM Act uses exchange values which are numerically 
equivalent to the 100-year GWP of the chemical as given in the 
Errata to Table 2.14 of the IPCC's 2007 Fourth Assessment Report 
(AR4).
---------------------------------------------------------------------------

    In the United States, HFCs are used primarily in refrigeration and 
air-conditioning equipment in homes, commercial buildings, and 
industrial operations (~75 percent of total HFC use in 2018) and in air 
conditioning in vehicles and refrigerated transport (~8 percent). 
Smaller amounts are used in foam products (~11 percent), aerosols (~4 
percent), fire protection systems (~1 percent), and solvents (~1 
percent).\19\
---------------------------------------------------------------------------

    \19\ Calculations based on EPA's Vintaging Model, which 
estimates the annual chemical emissions from industry sectors that 
historically used ODS, including refrigeration and air conditioning, 
foam blowing agents, solvents, aerosols, and fire suppression. The 
model uses information on the market size and growth for each end 
use, as well as a history and projections of the market transition 
from ODS to substitutes. The model tracks emissions of annual 
``vintages'' of new equipment that enter into operation by 
incorporating information on estimates of the quantity of equipment 
or products sold, serviced, and retired or converted each year, and 
the quantity of the compound required to manufacture, charge, and/or 
maintain the equipment. Additional information on these estimates is 
available in U.S. EPA, April 2016. EPA Report EPA-430-R-16-002. 
Inventory of U.S. Greenhouse Gas Emissions and Sinks: 1990-2014. 
Available at: <a href="https://www.epa.gov/ghgemissions/inventory-us-greenhouse-gas-emissions-and-sinks-1990-2014">https://www.epa.gov/ghgemissions/inventory-us-greenhouse-gas-emissions-and-sinks-1990-2014</a>.
---------------------------------------------------------------------------

    EPA estimated in the Allocation Rules that phasing down HFC 
production and consumption according to the schedule provided in the 
AIM Act will avoid cumulative consumption of 3,156 million metric tons 
of exchange value equivalent (MMTEVe) of HFCs in the United States for 
the years 2022 through 2036 (86 FR 55116, October 5, 2021). Annual 
avoided consumption was estimated at 42 MMTCO<INF>2</INF>e in 2022 and 
282 MMTCO<INF>2</INF>e in 2036. To calculate the climate benefits 
associated with consumption abatement, the consumption changes were 
expressed in terms of emission reductions. EPA estimated that for the 
years 2022-2050 that action will avoid emissions of 4,560 
MMTCO<INF>2</INF>e of HFCs in the United States. The annual avoided 
emissions are estimated at 22 MMTCO<INF>2</INF>e in the year 2022 and 
171 MMTCO<INF>2</INF>e in 2036. More information regarding these 
estimates is provided in the Allocation Framework RIA in the docket.

B. How do HFCs affect public health and welfare?

    Elevated concentrations of GHGs including HFCs are and have been 
warming the planet, leading to changes in the Earth's climate including 
changes in the frequency and intensity of heat waves, precipitation, 
and extreme weather events; rising seas; and retreating snow and ice. 
The changes taking place in the atmosphere as a

[[Page 73105]]

result of the well-documented buildup of GHGs due to human activities 
are changing the climate at a pace and scale that threatens human 
health, society, and the natural environment. This section provides 
some scientific background on climate change to offer additional 
context for this rulemaking and to help the public understand the 
environmental impacts of GHGs such as HFCs.
    Extensive additional information on climate change is available in 
the scientific assessments and the EPA documents that are briefly 
described in this section, as well as in the technical and scientific 
information supporting them. One of those documents is EPA's 2009 
Endangerment and Cause or Contribute Findings for Greenhouse Gases 
Under Section 202(a) of the Clean Air Act (74 FR 66496, December 15, 
2009).\20\ In the 2009 Endangerment Finding, the Administrator found 
under section 202(a) of the CAA that elevated atmospheric 
concentrations of six key well-mixed GHGs--CO<INF>2</INF>, methane 
(CH<INF>4</INF>), nitrous oxide (N<INF>2</INF>O), HFCs, 
perfluorocarbons (PFCs), and sulfur hexafluoride (SF<INF>6</INF>)--
``may reasonably be anticipated to endanger the public health and 
welfare of current and future generations'' (74 FR 66523, December 15, 
2009), and the science and observed changes have confirmed and 
strengthened the understanding and concerns regarding the climate risks 
considered in the Finding. The 2009 Endangerment Finding, together with 
the extensive scientific and technical evidence in the supporting 
record, documented that climate change caused by human emissions of 
GHGs (including HFCs) threatens the public health of the U.S. 
population. It explained that by raising average temperatures, climate 
change increases the likelihood of heat waves, which are associated 
with increased deaths and illnesses (74 FR 66497, December 15, 2009). 
While climate change also increases the likelihood of reductions in 
cold-related mortality, evidence indicates that the increases in heat 
mortality will be larger than the decreases in cold mortality in the 
U.S. (74 FR 66525, December 15, 2009). The 2009 Endangerment Finding 
further explained that compared with a future without climate change, 
climate change is expected to increase tropospheric ozone pollution 
over broad areas of the U.S., including in the largest metropolitan 
areas with the worst tropospheric ozone problems, and thereby increase 
the risk of adverse effects on public health (74 FR 66525, December 15, 
2009). Climate change is also expected to cause more intense hurricanes 
and more frequent and intense storms of other types and heavy 
precipitation, with impacts on other areas of public health, such as 
the potential for increased deaths, injuries, infectious and waterborne 
diseases, and stress-related disorders (74 FR 66525, December 15, 
2009). Children, the elderly, and the poor are among the most 
vulnerable to these climate-related health effects (74 FR 66498, 
December 15, 2009).
---------------------------------------------------------------------------

    \20\ In describing these 2009 Findings in this notice, EPA is 
neither reopening nor revisiting them.
---------------------------------------------------------------------------

    The 2009 Endangerment Finding also documented, together with the 
extensive scientific and technical evidence in the supporting record, 
that climate change touches nearly every aspect of public welfare \21\ 
in the U.S. including: changes in water supply and quality due to 
increased frequency of drought and extreme rainfall events; increased 
risk of storm surge and flooding in coastal areas and land loss due to 
inundation; increases in peak electricity demand and risks to 
electricity infrastructure; predominantly negative consequences for 
biodiversity and the provisioning of ecosystem goods and services; and 
the potential for significant agricultural disruptions and crop 
failures (though offset to some extent by carbon fertilization). These 
impacts are also global and may exacerbate problems outside the U.S. 
that raise humanitarian, trade, and national security issues for the 
United States (74 FR 66530, December 15, 2009).
---------------------------------------------------------------------------

    \21\ The CAA states in section 302(h) that ``[a]ll language 
referring to effects on welfare includes, but is not limited to, 
effects on soils, water, crops, vegetation, manmade materials, 
animals, wildlife, weather, visibility, and climate, damage to and 
deterioration of property, and hazards to transportation, as well as 
effects on economic values and on personal comfort and well-being, 
whether caused by transformation, conversion, or combination with 
other air pollutants.'' 42 U.S.C. 7602(h).
---------------------------------------------------------------------------

    In 2016, the Administrator similarly issued Endangerment and Cause 
or Contribute Findings for GHG emissions from aircraft under section 
231(a)(2)(A) of the CAA (81 FR 54422, August 15, 2016).\22\ In the 2016 
Endangerment Finding, the Administrator found that the body of 
scientific evidence amassed in the record for the 2009 Endangerment 
Finding compellingly supported a similar endangerment finding under CAA 
section 231(a)(2)(A) and also found that the science assessments 
released between the 2009 and the 2016 Findings ``strengthen and 
further support the judgment that GHGs in the atmosphere may reasonably 
be anticipated to endanger the public health and welfare of current and 
future generations'' (81 FR 54424, August 15, 2016).
---------------------------------------------------------------------------

    \22\ In describing these 2016 Findings in this notice, EPA is 
neither reopening nor revisiting them.
---------------------------------------------------------------------------

    Since the 2016 Endangerment Finding, the climate has continued to 
change, with new records being set for several climate indicators such 
as global average surface temperatures, GHG concentrations, and sea 
level rise. Moreover, heavy precipitation events have increased in the 
Eastern United States, while agricultural and ecological drought has 
increased in the Western United States along with more intense and 
larger wildfires.\23\ These and other trends are examples of the risks 
discussed in the 2009 and 2016 Endangerment Findings that have already 
been experienced. Additionally, major scientific assessments continue 
to demonstrate advances in our understanding of the climate system and 
the impacts that GHGs have on public health and welfare both for 
current and future generations. According to the Intergovernmental 
Panel on Climate Change's (IPCC) Sixth Assessment Report, ``it is 
unequivocal that human influence has warmed the atmosphere, ocean and 
land. Widespread and rapid changes in the atmosphere, ocean, cryosphere 
and biosphere have occurred.'' \24\ These updated observations and 
projections document the rapid rate of current and future climate 
change both globally and in the United States.<SUP>25 26 27 28</SUP>
---------------------------------------------------------------------------

    \23\ An additional resource for indicators can be found at 
<a href="https://www.epa.gov/climate-indicators">https://www.epa.gov/climate-indicators</a>.
    \24\ IPCC, 2021: Summary for Policymakers. In: Climate Change 
2021: The Physical Science Basis. Contribution of Working Group I to 
the Sixth Assessment Report of the Intergovernmental Panel on 
Climate Change [Masson-Delmotte, V., P. Zhai, A. Pirani, S.L. 
Connors, C. Pe[aacute]an, S. Berger, N. Caud, Y. Chen, L. Goldfarb, 
M.I. Gomis, M. Huang, K. Leitzell, E. Lonnoy, J.B.R. Matthews, T.K. 
Maycock, T. Waterfield, O. Yelek[ccedil]i, R. Yu and B. Zhou 
(eds.)]. Cambridge University Press. In Press: 4.
    \25\ USGCRP, 2018: Impacts, Risks, and Adaptation in the United 
States: Fourth National Climate Assessment, Volume II [Reidmiller, 
D.R., C.W. Avery, D.R. Easterling, K.E. Kunkel, K.L.M. Lewis, T.K. 
Maycock, and B.C. Stewart (eds.)]. U.S. Global Change Research 
Program, Washington, DC, USA, 1515 pp. doi: 10.7930/NCA4.2018. 
Available at: <a href="https://nca2018.globalchange.gov">https://nca2018.globalchange.gov</a>.
    \26\ IPCC, 2021.
    \27\ National Academies of Sciences, Engineering, and Medicine, 
2019. Climate Change and Ecosystems. Washington, DC: The National 
Academies Press. Available at: <a href="https://doi.org/10.17226/25504">https://doi.org/10.17226/25504</a>.
    \28\ NOAA National Centers for Environmental Information, State 
of the Climate: Global Climate Report for Annual 2020, published 
online January 2021. Available at: <a href="https://www.ncdc.noaa.gov/sotc/global/202013">https://www.ncdc.noaa.gov/sotc/global/202013</a>.

---------------------------------------------------------------------------

[[Page 73106]]

IV. What is the petition process under the technology transitions 
program?

    Subsection (i)(3) of the AIM Act states that a person may petition 
EPA to promulgate a rule to restrict the use of a regulated substance 
in a sector or subsector in accordance with the Agency's authority to 
issue such a rule under subsection (i)(1) of the AIM Act. If EPA 
receives a petition under subsection (i)(3), the AIM Act states that 
``[t]he Administrator shall grant or deny a petition . . . not later 
than 180 days after the date of receipt of the petition'' (42 U.S.C. 
7675(i)(3)(B)) and make the petition available to the public no later 
than 30 days after receiving the petition (42 U.S.C. 
7675(i)(3)(C)(iii)). For petitions that are denied, EPA must publish in 
the Federal Register an explanation of the denial (42 U.S.C. 
7675(i)(3)(C)(i)). If EPA grants a petition, the statute requires EPA 
to promulgate a final rule not later than two years from the date the 
Agency grants the petition (42 U.S.C. 7675(i)(3)(C)(ii)).
    This section describes the process for submitting a petition under 
subsection (i) to the Agency, which includes direction on how 
technology transition provisions should be submitted to EPA; the 
necessary content of petitions; and how EPA will respond once petitions 
are received. EPA received comments in support of the Agency's 
interpretation of the petition process under the AIM Act. Commenters 
did not suggest any changes to the proposed petition process. EPA is 
finalizing the petition process as proposed.
    Subsection (i)(3)(A) of the AIM Act states that ``a person may 
petition the Administrator to promulgate a rule under [subsection 
(i)(1) of the AIM Act] for the restriction on use of a regulated 
substance in a sector or subsector, which shall include a request that 
the Administrator negotiate with stakeholders . . .'' EPA views 
``person'' for the purpose of a technology transitions petition 
submittal as having the same meaning as how the term is defined in 40 
CFR 84.3 (the definition established in the Allocation Framework Rule); 
that is, to mean ``any individual or legal entity, including an 
individual, corporation, partnership, association, state, municipality, 
political subdivision of a State, Indian Tribe; any agency, department, 
or instrumentality of the United States; and any officer, agent, or 
employee thereof.'' Using this definition in 40 CFR 84.3 for purposes 
of petition submittal under subsection (i) ensures consistency of how 
this term is used across these two regulatory programs developed under 
the AIM Act. This definition of ``person'' also captures the Agency's 
intended meaning of this term for purposes of the Technology 
Transitions program. Therefore, any person who fits the Allocation 
Framework Rule definition may submit a technology transitions petition 
to EPA. We further note that the plain text of subsection (i)(3)(A) 
also limits this provision to requests for restrictions on the use of a 
regulated substance in a sector or subsector. Other types of requests--
such as exemptions from existing or anticipated restrictions--are 
therefore not properly presented under the (i)(3)(A) petition process, 
although parties are always welcome to communicate to the Agency 
informally, to provide comments on a proposed rule that considers such 
restrictions on use, or to generally petition for rulemaking under the 
Administrative Procedures Act.
    All the petitions considered in this rulemaking were submitted to 
EPA via email. EPA is requiring that future petitions also be submitted 
electronically. The Agency's preferred method is for petitioners to use 
the email address that is available on EPA's web page at: <a href="https://www.epa.gov/climate-hfcs-reduction/technology-transition-petitions-under-aim-act">https://www.epa.gov/climate-hfcs-reduction/technology-transition-petitions-under-aim-act</a>.

A. What must be included in a technology transitions petition?

    EPA is requiring standard content that must be included in a 
technology transitions petition. Standardizing the information 
requirements will assist petitioners in preparing their petitions and 
enhance EPA's ability to review and respond to them promptly. A 
technology transitions petition must include the elements described in 
the following paragraphs.
    Petitions must indicate either a GWP limit or the specific name(s) 
of the regulated substance(s) or blend(s) that use the regulated 
substance(s) to be restricted and their GWPs. Petitioners specifying 
specific regulated substances should use as the GWP the exchange values 
for the regulated HFCs listed in subsection (c) of the AIM Act and 
codified as appendix A to 40 CFR part 84.\29\ For blends containing 
regulated substances, petitioners should identify all components of the 
blend using the composition-identifying designation as listed in 
American National Standards Institute/American Society of Heating, 
Refrigerating and Air-Conditioning Engineers (ANSI/ASHRAE) Standard 34-
2022,\30\ Designation and Safety Classification of Refrigerants (e.g., 
HFC-134a, hydrofluoroolefin (HFO-1234ze(E)). If blends are not listed 
in ASHRAE Standard 34, petitioners should provide the nominal 
composition of the blend, specifying all components with the ASHRAE 
Standard 34 designation for the components. If the components or 
substances are not listed in ASHRAE Standard 34, petitioners should 
provide the chemical name, the applicable CAS Registry Number, and the 
chemical formula and structure (e.g., CHF=C=CF<INF>2</INF> rather than 
C<INF>3</INF>F<INF>3</INF>H).
---------------------------------------------------------------------------

    \29\ EPA noted in section III.A of this preamble that the 
exchange values for the regulated HFCs listed in subsection (c) of 
the AIM Act are numerically identical to the 100-year GWPs of each 
substance, as given in the Errata to Table 2.14 of the IPCC's Fourth 
Assessment Report (AR4) and Annexes A, C, and F of the Montreal 
Protocol. Available at: <a href="https://www.ipcc.ch/site/assets/uploads/2018/05/ar4-wg1-errata.pdf">https://www.ipcc.ch/site/assets/uploads/2018/05/ar4-wg1-errata.pdf</a>.
    \30\ Hereafter referred to as ASHRAE Standard 34.
---------------------------------------------------------------------------

    EPA is providing a table at 40 CFR 84.64 listing the GWPs of 
commonly used constituents to allow petitioners to determine the GWP of 
blends containing regulated substances for purposes of this rulemaking. 
EPA also intends to maintain a list of commonly used blends containing 
HFCs and the GWPs of those blends at EPA's Technology Transitions web 
page. EPA is using the following hierarchy to identify the GWPs of 
these constituents. For the regulated substances used in the blend, and 
as previously noted, EPA is using the exchange value provided in 
subsection (c) of the AIM Act and codified as appendix A to 40 CFR part 
84 as the GWP. For purposes of this rulemaking EPA is using the 100-
year GWP values from the IPCC's Fourth Assessment Report (AR4) for all 
substances or components of blends. For hydrocarbons listed in Table 2-
15 of AR4, EPA is using the net GWP value. For substances for which no 
GWP is provided in AR4, EPA is using the 100-year GWP listed in World 
Meteorological Organization (WMO) 2022.\31\ EPA proposed using the 2018 
edition but to use the best available data, EPA is finalizing the use 
of the most up-to-date version of this report at the time of the 
publication of this rule. For any substance not listed in these 
sources, EPA is using the GWP of the substance in Table A-1 to subpart 
A of 40 CFR part 98, as it exists on October 24, 2023, the date this 
rule is published in the Federal Register as a final rule, if such 
substance is specifically listed in that table. EPA proposed GWPs for 
two substances that might be used as components of blends that are not 
listed in those three sources: trans-dichloroethylene (HCO-1130(E)) and 
hydrochlorofluoroolefin (HCFO-

[[Page 73107]]

1224yd(Z)) at five \32\ and one,\33\ respectively, for purposes of this 
rulemaking. EPA is finalizing those GWPs as proposed. For any other 
substance not listed in the above three source documents, EPA is using 
the default GWPs as shown in Table A-1 to subpart A of 40 CFR part 98, 
as it exists on the date this final rule is published in the Federal 
Register. Lastly, if the substance is not listed in any of the other 
sources, EPA is using the GWP of that constituent described in a 
listing of an acceptable substitute under EPA's SNAP program. In any 
case where a GWP value is preceded with a less than (<), very less than 
(<<), greater than (>), approximately (~), or similar symbol in the 
source document, which is used to determine the GWP, EPA is using the 
value shown. The GWP of a blend would then be calculated as the sum of 
the nominal composition (in mass proportions) of each component 
multiplied by the GWP of each component.
---------------------------------------------------------------------------

    \31\ WMO, 2022.
    \32\ 81 FR 32244 (May 23, 2016).
    \33\ 84 FR 64766 (November 25, 2019).
---------------------------------------------------------------------------

    In the event that the hierarchy outlined in this section does not 
provide a GWP (i.e., the substance in question is not listed in the 
three documents, is not one of the two for which EPA is establishing 
GWPs, is not listed in Table A-1 to subpart A of 40 CFR part 98 and 
does not fit within any of the default GWPs provided in Table A-1 to 
subpart A of 40 CFR part 98), EPA proposed that the petitioner should 
use a GWP of zero. One commenter suggested that using a value of zero 
would result in an artificially lower GWP value. Although EPA 
anticipates this situation to be rare, and unlikely to materially 
affect the status of a blend, the Agency is not assuming a value of 
zero for as yet unknown constituents in this final rule. Rather, EPA 
will take a more conservative approach and exclude that component, and 
its mass proportion, from the calculation of GWP.
    Petitioners must also indicate the sector or subsector for which 
restrictions on use of the regulated substance would apply. EPA is not 
limiting sectors or subsectors to a specific list, recognizing there 
may be additional uses of HFCs today or that may be developed in the 
future, and thus additional sectors or subsectors for which it could be 
appropriate to restrict use.
    Petitioners must specify a date that the requested restrictions 
would go into effect and provide information explaining why the date is 
appropriate. Petitioners should recognize that subsection (i)(6) of the 
AIM Act restricts the effective date of rules promulgated under 
subsection (i) to no earlier than one year after the date of the final 
rule.
    Before proposing a rule for the use of a regulated substance for a 
sector or subsector under subsection (i)(1), subsection (i)(2)(A) 
directs EPA to consider negotiating with stakeholders in accordance 
with the Negotiated Rulemaking Act of 1990 (i.e., negotiated rulemaking 
procedure). Subsection (i)(3)(A) requires petitioners to ``include a 
request that the Administrator negotiate with stakeholders in 
accordance with paragraph (2)(A)'' (42 U.S.C. 7675(i)(3)(A)). EPA 
sought comment on whether it is reasonable for the Agency to interpret 
subsection (i)(3) as requiring petitioners to address whether EPA use 
the negotiated rulemaking procedure, rather than requiring them to 
affirmatively request that the Agency pursue negotiated rulemaking. 
Several commenters responded in support of EPA's interpretation that 
petitioners must simply address whether EPA should consider negotiated 
rulemaking in their petition and not that they must request a 
negotiated rulemaking. Most petitions addressed in this rule complied 
with the statute's requirement to request that EPA use negotiated 
rulemaking; however, those petitioners unanimously expressed a 
preference that EPA not use this procedure in promulgating its 
restrictions. Allowing petitioners to express their views as to whether 
EPA should engage in negotiated rulemaking for a subsection (i) 
rulemaking, as opposed to requiring them to request something they may 
disagree with, provides more value to EPA as we consider, per 
subsection (i)(2)(A), whether to use the negotiated rulemaking 
procedure before proposing a restriction under subsection (i). 
Otherwise, EPA could be misled as to the petitioners' views and could 
elect to use the negotiated rulemaking procedure when no stakeholder 
sought that outcome. The unwarranted use of time and resources to 
undergo that procedure could be counterproductive to meeting the 
statutory deadlines to complete a final rule. Petitioners must provide 
an explanation of their position on the use of the negotiated 
rulemaking procedure and any considerations that would either support 
or disfavor the use of that process. If a petition is granted, EPA 
intends to consider the petitioner's statement on negotiated rulemaking 
as it determines whether to use the procedure.
    Petitioners must also submit, to the extent practicable, 
information related to the ``Factors for Determination'' listed in 
subsection (i)(4) of the AIM Act to facilitate EPA's review of the 
petition. Given the relatively short 180-day statutory timeframe for 
EPA to grant or deny a petition, this requirement will ensure that 
information is available to EPA at the start of its review, to the 
extent the petitioner has relevant available information. EPA may deny 
a petition where no information has been provided that would allow the 
Agency to act on the petition. Therefore, petitioners must, to the 
extent practicable, provide best available data on substitutes that 
could be used in lieu of the petitioned substance(s), addressing the 
subfactors (e.g., technological achievability, safety, commercial 
demands, etc.) that may affect the availability of those substitutes. 
Other relevant information includes estimates of the economic costs and 
environmental impacts of the petitioner's requested restriction on use 
in the sector or subsector. In particular, providing EPA with a sense 
of the scale of impacts (e.g., whether the suggested restriction would 
have a significant environmental impact, or whether the suggested 
restriction would be likely to impose costs or savings on regulated 
entities or consumers) using best available, quantitative, accurate 
data to support that assessment will be more likely to result in a 
timely, well-reasoned response to the petitioner's request. One 
commenter suggested that EPA require that petitions include information 
on the expected outcome of requests made in the petition with respect 
to the consumption and emissions of regulated substances. The commenter 
indicated that this could be done by sharing assumptions regarding 
equipment charge size, leak rate, lifespan, and national sales. While 
EPA agrees that this information may be useful for assessing 
petitioners' requests as they relate to environmental impacts and other 
(i)(4) factors, the Agency disagrees that this information should be a 
mandatory element of the petitions, as many petitioners may not know 
the expected outcome of their petition requests as it relates to the 
consumption and emissions of regulated substances.

B. What happens after a petition is submitted?

    Subsection (i)(3)(C)(iii) instructs EPA to make petitions publicly 
available within 30 days after receipt. EPA intends to continue to post 
technology transitions petitions at <a href="http://www.regulations.gov">www.regulations.gov</a>, in Docket ID 
No. EPA-HQ-OAR-2021-0289, as well as on the Agency's website at <a href="https://www.epa.gov/climate-hfcs-reduction/technology-transition-petitions-under-aim-act">https://www.epa.gov/climate-hfcs-reduction/technology-transition-petitions-under-aim-act</a>. Making the petitions available

[[Page 73108]]

allows the public to provide additional data and relevant material to 
aid in EPA's evaluation of petitions, based on the factors specified in 
subsection (i) of the AIM Act.
    In accordance with the statutory directive, EPA intends to act on 
petitions no later than 180 days after the date of receipt of the 
petition. In making a determination to grant or deny a petition, 
subsection (i)(4) of the AIM Act requires EPA to consider, to the 
extent practicable:
    1. The best available data;
    2. The availability of substitutes for use of the regulated 
substance that is the subject of the rulemaking or petition, as 
applicable, in a sector or subsector, taking into account technological 
achievability, commercial demands, affordability for residential and 
small business consumers, safety, consumer costs, building codes, 
appliance efficiency standards, contractor training costs, and other 
relevant factors, including the quantities of regulated substances 
available from reclaiming, prior production, or prior import;
    3. Overall economic costs and environmental impacts, as compared to 
historical trends; and
    4. The remaining phase-down period for regulated substances under 
the final rule issued under subsection (e)(3) of the AIM Act, if 
applicable.
    Subsection (i)(4) applies both to EPA's action on subsection (i) 
petitions and to EPA's rulemakings under subsection (i). Requiring EPA 
to grant or deny petitions within 180 days of receipt inherently limits 
the scope and depth of any potential analysis. EPA's timeframe for 
promulgating a rule subject to a granted petition is two years from the 
date of a petition grant, and in undertaking a rulemaking the Agency 
will undoubtedly be able to perform a more in-depth analysis of the 
(i)(4) factors. Granting a petition under subsection (i) of the AIM Act 
therefore does not necessarily mean the Agency will propose or finalize 
requirements identical to a petitioner's request. Rather, granting a 
petition means that the requested restriction warrants further 
consideration through rulemaking. During this rulemaking process, EPA 
will determine what restrictions on the use of HFCs to propose and 
finalize based on multiple considerations, including its consideration 
of the ``Factors for Determination'' listed in subsection (i)(4) to the 
extent practicable. This approach provides interested stakeholders with 
the opportunity to review and comment on a regulatory proposal 
restricting the use of HFCs prior to restrictions going into effect.

C. Can I revise or resubmit my petition?

    Receipt of a completed petition triggers two statutory deadlines: 
the posting of the petition within 30 days and the granting or denying 
of the petition within 180 days. Because there is little purpose in EPA 
continuing to take action on the original petition when the petitioner 
has revised (i.e., makes edits to an original request) or resubmitted 
(i.e., makes edits to an original request and presents it as a new 
petition) it, EPA's view is that a petition revision or resubmittal 
made by petitioners is typically intended to supersede or replace the 
original petition and would thus restart these timelines. However, 
depending on the timing of the resubmission and the nature of the 
revision and the request, EPA may be able to act more quickly on a 
revised or resubmitted petition, for example, if the Agency had already 
developed familiarity with the request through its consideration of the 
original petition. Therefore, EPA intends to address petition revisions 
and resubmittals on a case-by-case basis. If petitioners do not intend 
for their submission to supersede or replace their original petition, 
rather they are submitting information to revise or augment their 
initial petition without significantly altering its scope, they should 
be clear that they are submitting supplemental or clarifying 
information regarding their petitions to the docket related to 
petitions under consideration. On a case-by-case basis the Agency will 
consider and act accordingly on supplemental or clarifying information 
as part of its consideration of the initial petition. If EPA finds that 
in fact what was submitted constitutes a new petition or revised 
petition, new timelines will apply. In making a determination to grant 
or deny petitions, EPA plans to consider relevant and timely 
information provided in this docket, as the Agency did with the granted 
petitions that led to this rulemaking, including information provided 
by petitioners and from other stakeholders, for those petitions under 
review. Once a petition is granted or denied, any revised or 
resubmitted petitions will likely be treated as a new petition.

V. How is EPA considering negotiated rulemaking?

    This section provides a summary of the AIM Act's directive to 
consider negotiating with stakeholders prior to proposing a rule under 
subsection (i) of the Act. This section also provides information 
regarding how EPA intends to consider negotiating with stakeholders for 
future rulemakings.

A. Summary of the AIM Act's Directive on Negotiated Rulemaking

    Prior to proposing a rule, subsection (i)(2)(A) of the Act directs 
EPA to consider negotiating with stakeholders in the sector or 
subsector subject to the potential rule in accordance with negotiated 
rulemaking procedures established under the ``Negotiated Rulemaking Act 
of 1990.'' If EPA makes a determination to use the negotiated 
rulemaking procedures, subsection (i)(2)(B) requires that EPA, to the 
extent practicable, give priority to completing that rulemaking over 
completing rulemakings under subsection (i) that are not using that 
procedure. For additional information on negotiated rulemaking 
procedures, see 5 U.S.C. 563. If EPA does not use the negotiated 
rulemaking process, subsection (i)(2)(C) requires the Agency to publish 
an explanation of the decision to not use that procedure before 
commencement of the rulemaking process.

B. How does EPA intend to consider negotiating with stakeholders under 
the AIM Act?

    Prior to proposing this rulemaking, EPA issued a document informing 
the public of the Agency's consideration of using the negotiated 
rulemaking procedure and the Agency's decision to not use these 
procedures for this rulemaking (86 FR 74080, December 29, 2021). The 
Agency found that using negotiated rulemakings was not in the best 
interest of the public and thus decided not to use negotiated 
rulemaking. In making this decision, EPA considered information 
provided by the petitions, including statements made by petitioners on 
the use of negotiated rulemaking procedures, and information provided 
by other stakeholders on the petitions. The Negotiated Rulemaking Act 
of 1990, 5 U.S.C. 563, provides seven criteria that the head of an 
agency should consider when determining whether a negotiated rulemaking 
is in the public interest. These criteria are informative for purposes 
of making a determination under AIM Act subsection (i) of whether to 
use the procedures set out in the Negotiated Rulemaking Act for 
proposed rulemakings and therefore, also considered these criteria in 
its decision.
    Going forward, EPA intends to use a similar process in making its 
determination on whether to use negotiated rulemaking procedures for 
any rulemaking being considered under subsection (i) in response to 
granted

[[Page 73109]]

petitions. This includes reviewing the petitions themselves and 
statements from petitioners on the use of negotiated rulemaking 
procedures, considering information provided by stakeholders commenting 
on petitions, and considering the seven criteria listed in the 
Negotiated Rulemaking Act of 1990, 5 U.S.C. 563, that the head of an 
agency should consider when determining whether a negotiated rulemaking 
is in the public's interest. For rulemakings initiated by EPA (i.e., 
not in response to granted petitions), EPA anticipates that our review 
would focus on just these seven criteria.
    Furthermore, where appropriate, EPA will also consider recent 
Agency actions and decisions related to restrictions on the use of HFCs 
in sectors and subsectors for its consideration on using negotiated 
rulemaking procedures. For example, EPA received four petitions that 
were not included in the Agency's consideration of using negotiated 
rulemaking procedures for petitions granted on October 7, 2021.\34\ 
However, these petitions requested restrictions on the use of HFCs in 
the same sectors and subsectors covered by petitions granted on October 
7, 2021, for which EPA made a determination not to use negotiated 
rulemaking. Subsection (i)(2)(A) states that, ``[b]efore proposing a 
rule for a sector or subsector under paragraph (1), the Administrator 
shall consider negotiating with stakeholders in the sector or subsector 
subject to the potential rule . . .'' EPA will not issue a separate 
notice to consider using negotiated rulemaking for these four petitions 
because these petitions were received well ahead of this final action, 
and the requested restrictions are in the same sectors and subsectors 
contained in petitions granted on October 7, 2021, for which the Agency 
considered and decided not to use negotiated rulemaking procedures. 
Nothing in these four petitions caused EPA to reconsider that decision. 
Therefore, it is unnecessary for the Agency to reconsider whether to 
use negotiated rulemaking procedures for this rulemaking. EPA 
encourages future petitioners to consider petitions under review or 
recently granted before submitting a new petition and to consider 
submitting information to the docket for an existing petition in lieu 
of submitting a new petition on the same uses of HFCs that are already 
under consideration by the Agency.
---------------------------------------------------------------------------

    \34\ These petitions were received from AHRI and IIAR and are 
discussed in section VI.D of this preamble. Copies of these 
petitions are located at <a href="http://www.regulations.gov">www.regulations.gov</a>, under Docket ID No. 
EPA-HQ-OAR-2021-0289, or at <a href="https://www.epa.gov/climate-hfcs-reduction/technology-transition-petitions-under-aim-act">https://www.epa.gov/climate-hfcs-reduction/technology-transition-petitions-under-aim-act</a>.
---------------------------------------------------------------------------

    One commenter requested that EPA conduct a negotiated rulemaking in 
instances where the Agency grants a petition but then would seek to 
propose more stringent aspects of the request, such as an earlier 
compliance date or lower GWP limit. EPA disagrees with this comment. A 
decision by the Agency to grant, or partially grant, a petition under 
subsection (i) of the AIM Act does not mean the Agency must propose 
requirements identical to a petitioner's request. Rather, granting a 
petition means that the requested restriction warrants further 
consideration through rulemaking. Furthermore, given the interests of 
all stakeholders including potentially other petitioners, it would not 
be appropriate to consider a negotiated rulemaking only when EPA is 
considering a more stringent proposal. EPA therefore may consider 
whether any deviation from a petition merits a negotiated rulemaking in 
its analysis of the public's interest, but a deviation on its own is 
insufficient to require the Agency to do so.

VI. How is EPA restricting the use of HFCs?

    This section details the Agency's restrictions on the use of HFCs 
in accordance with the granted petitions, including defining terms that 
are new to 40 CFR part 84; describing the form and applicability of the 
prohibitions; providing EPA's interpretation and application of the 
``Factors for Determination'' contained in subsection (i)(4) of the AIM 
Act; and listing the specific restrictions on the use of HFCs by sector 
and subsector.

A. What definitions is EPA establishing in subsection (i)?

    The Allocation Framework Rule established regulatory definitions at 
40 CFR part 84, subpart A to implement the regulatory phasedown of HFCs 
under the AIM Act. To maintain consistency, except as otherwise 
explained in this rule, EPA intends to use terms in this rulemaking, 
and in the new subpart B established by this rule, as they were defined 
in the Allocation Framework Rule. Thus, for terms not defined in this 
subpart but that are defined in 40 CFR 84.3, the definitions in 40 CFR 
84.3 shall apply. EPA is also establishing definitions for new terms 
that are applicable to 40 CFR part 84, subpart B and do not have a 
counterpart in the definitions under 40 CFR part 84, subpart A.
1. Export, Exporter, Import, and Importer
    A few terms (export, exporter, and importer) currently exist in 40 
CFR 84.3 in the context of bulk regulated substances. EPA is 
establishing definitions under subpart B for those terms to clarify how 
they apply under subpart B to regulated substances that are used in 
equipment subject to this rule.
    Export. For purposes of subpart B, EPA is defining this term to 
mean the transport of a product or specified component using a 
regulated substance from inside the United States or its territories to 
persons outside the United States or its territories, excluding United 
States military bases and ships for onboard use.
    Exporter. For purposes of subpart B, EPA is defining this term to 
mean the person who contracts to sell any product or specified 
component using a regulated substance for export or transfers a product 
or specified component using a regulated substance to an affiliate in 
another country.
    Importer. For purposes of subpart B, EPA is defining this term to 
mean any person who imports any product or specified component using or 
intended for use with a regulated substance into the United States. 
Importer includes the person primarily liable for the payment of any 
duties on the merchandise or an authorized agent acting on his or her 
behalf. The term also includes:
    (1) The consignee;
    (2) The importer of record;
    (3) The actual owner; or
    (4) The transferee, if the right to withdraw merchandise from a 
bonded warehouse has been transferred.
    This definition of importer, specifically paragraphs (3) and (4), 
varies in non-substantive ways from that in subpart A of 40 CFR part 84 
to align with the definition of ``importer'' at 19 CFR 101.1. No 
difference in interpretation between subparts is intended. As EPA 
explained in the Allocation Framework Rule, whether products using or 
containing HFCs are admitted into or exiting from a foreign-trade zone 
or other duty deferral program under U.S. Customs and Border Protection 
(CBP) regulations does not affect whether they are being imported or 
exported for purposes of part 84. See 86 FR 55133 (October 5, 2021) 
(discussing definitions of export and import under 40 CFR 84.3).
    Comment: Some commenters requested that EPA narrow the scope of the 
term ``import'' to exclude a transportation vehicle in international 
service, such as refrigerated containers

[[Page 73110]]

that are imported into the United States and intended for export. 
Another commenter requested that the definition of import include 
equipment that was intended to be imported by the date but was delayed 
by weather or port delays.
    Response: EPA disagrees with these suggestions. Congress defined 
``import'' for purposes of the AIM Act in subsection (b)(6) as ``to 
land on, bring into, or introduce into, or attempt to land on, bring 
into, or introduce into, any place subject to the jurisdiction of the 
United States, regardless of whether that landing, bringing, or 
introduction constitutes an importation within the meaning of the 
customs laws of the United States.'' The Agency did not propose to 
redefine that term in this subpart. EPA addresses the concern raised by 
the first commenter in Section VI.C.2.a. Furthermore, to be consistent 
with subpart A of part 84, EPA considers the date of import to be the 
time a ship berths for vessel arrivals, border crossings for land 
arrivals, and first point of terminus in U.S. jurisdiction for arrivals 
via air. Determining an importer's intent for their timing, which 
frequently can change, would be challenging for the Agency to determine 
and enforce.
2. Blend Containing a Regulated Substance, Sector, Subsector, and 
Substitute
    EPA is finalizing definitions for these four terms as proposed. The 
Agency did not receive comment recommending changes.
    Blend containing a regulated substance. EPA is establishing 
restrictions on the use of HFCs, whether neat or used in a blend. 
Blends containing a regulated substance are used in multiple sectors 
and subsectors including refrigeration, air conditioning and heat 
pumps, foams, and fire suppression. EPA is defining this term as ``any 
mixture that contains one or more regulated substances.'' EPA considers 
any quantity of a regulated substance within a mixture to qualify the 
mixture as a ``blend containing a regulated substance.'' A blend that 
uses one or more regulated substances is itself not a regulated 
substance. Rather, the use restrictions apply to the regulated 
substance(s) used in certain blends, such that the use restriction on 
the regulated substance(s) also affects use of that blend. Most HFCs 
used in the sectors and subsectors addressed by this rule are 
components of blends that contain other HFCs, HFOs, and hydrocarbons. 
As discussed in section IV.A, where the proportion of a regulated 
substance multiplied by its GWP, along with the proportion of the other 
components multiplied by their respective GWPs, causes the blend to 
exceed the GWP limit, the use of that HFC in that blend is prohibited.
    Sector. EPA is defining this term as ``a broad category of 
applications including but not limited to: refrigeration, air 
conditioning and heat pumps; foams; aerosols; chemical manufacturing; 
cleaning solvents; fire suppression and explosion protection; and 
semiconductor manufacturing.'' These categorizations and groupings are 
similar to how the term ``sector'' is used in other contexts, such as 
EPA's Significant New Alternatives Policy (SNAP) Program, the Montreal 
Protocol Parties' Technology and Economic Assessment Panel (TEAP), and 
EPA's Vintaging Model. Entities potentially subject to rulemakings 
under subsection (i) of the AIM Act are often the same entities 
affected by CAA title VI, including the CAA section 612 SNAP program, 
and may be familiar with the way EPA traditionally categorizes and 
groups sectors in that context. The TEAP is a globally recognized 
advisory body to the Montreal Protocol Parties, which provides 
technical information related to alternative technologies that use HFCs 
in sectors and subsectors. Entities with a global market presence and 
other stakeholders may be familiar with how the TEAP defines sectors, 
and EPA's definition of sector is relatable to their understanding of 
the term.
    Subsector. EPA is defining this term as ``processes, classes of 
applications, or specific uses that are related to one another within a 
single sector or subsector.'' Where appropriate, each sector can be 
subdivided into different subsectors that more narrowly highlight how 
the HFC is used. Entities potentially subject to rulemakings under 
subsection (i) of the AIM Act are often the same entities affected by 
CAA title VI, including the CAA section 612 SNAP program, and may be 
familiar with the way EPA categorizes and groups sectors and subsectors 
in that context. The term ``subsectors'' includes the concepts of 
``end-uses'' and ``applications'' under SNAP (40 CFR 82.172). An 
example subsector is cold storage warehouses within the RACHP sector. 
Another example is the integral skin polyurethane subsector within the 
foams sector.
    Substitute. EPA is defining this term as ``any substance, blend, or 
alternative manufacturing process, whether existing or new, that may be 
used, or is intended for use, in a sector or subsector with a 
restriction on the use of regulated substances and that has a lower 
global warming potential than the GWP limit or restricted list of 
regulated substances and blends in that sector or subsector.'' Under 
this definition, substitutes include regulated substances (e.g., HFC-32 
used in lieu of R-410A in commercial unitary AC), blends containing 
regulated substances (e.g., R-454B used in lieu of R-410A in 
residential unitary AC), blends that do not use a regulated substance 
(e.g., R-441A used in lieu of R-410A in window ACs), substances that 
are not HFCs (e.g., HFOs, hydrocarbons, R-717, and R-744 
(CO<INF>2</INF>)), and not-in-kind technologies (e.g., finger-pump 
bottles in lieu of aerosol cans, or vacuum panels in lieu of foam 
insulation).
3. Manufacture, Install, and System
    Many commenters expressed concerns about the proposed definitions 
for the terms ``manufacture'' and ``products.'' For the reasons 
discussed in this section, EPA is distinguishing in this final rule 
between factory-completed and field-assembled appliances by defining 
and using the terms ``products'' and ``systems,'' respectively. EPA is 
also distinguishing between the ``manufacture'' of products, which 
occurs in a factory, and the ``installation'' of systems, which occurs 
in the field. Together these changes more clearly represent the intent 
of the restrictions using more familiar terminology.
    EPA proposed to define ``manufacture'' as ``to complete a product's 
manufacturing and assembly processes such that it is ready for initial 
sale, distribution, or operation. For equipment that is assembled and 
charged in the field, manufacture means to complete the circuit holding 
the regulated substance, charge with a full charge, and otherwise make 
functional for use for its intended purpose.'' This proposed definition 
was intended to apply similarly to how EPA applied this term in certain 
other use restrictions under title VI of the CAA and 40 CFR part 82. 
EPA had previously established restrictions on products, including 
appliances, foams, and aerosols under section 610 of the CAA 
(Nonessential Products Bans). EPA also established use prohibitions 
under section 605(a) of the CAA that addressed the use of certain ODS 
as a refrigerant in the manufacture of new appliances, including field-
charged appliances. See e.g., 40 CFR 82.15(g)(4)(i), 40 CFR 
82.15(g)(5)(i); see also 74 FR 66437 (December 15, 2009) and 85 FR 
15267 (March 17, 2020) (describing the use restriction and when a 
field-charged appliance is manufactured). Because those restrictions 
bear certain similarities to the proposed restrictions under subsection 
(i), EPA looked to its

[[Page 73111]]

past experience in implementing those provisions in defining 
``manufacture.''
    Comment: Commenters were generally supportive of the first sentence 
of the proposed definition of ``manufacture'' as applied to factory-
completed products. Most of those who commented on the proposed 
definition expressed concerns about the second sentence, which would 
apply to field-assembled equipment. These included concerns that the 
definition would effectively accelerate the timeline of the prohibition 
and render the one-year sell-through moot. Commenters stated that the 
Agency should be placing the prohibition on the manufacture of 
components that would later be assembled and not the installation. 
Commenters also suggested EPA use the approach taken by California in 
defining ``date of manufacture.'' In California, the date of 
manufacture for chillers and air-conditioning and refrigeration 
equipment that is not assembled on site is ``the date that the 
manufacturer affixed an equipment label indicating the equipment's date 
of manufacture.'' For refrigeration and air-conditioning equipment 
completed on site, the date of manufacture is ``the date that the 
refrigerant circuit was completed and initially filled with 
refrigerant.'' One equipment manufacturer urged harmonizing the Federal 
and California definitions to simplify manufacturers' obligations and 
reduce inadvertent noncompliance. The commenter noted that the 
definition resulted from substantial regulated industry discussions 
with and comments to the California Air Resources Board (CARB) during 
the State rulemaking process. Commenters acknowledged the need to 
address installation of field-charged equipment, but one commenter 
asserted that using the term ``manufacture'' created confusion about 
which entity would be considered the manufacturer of field-charged 
equipment, who would be both affected by the prohibition and subject to 
recordkeeping and reporting obligations.
    Response: EPA is finalizing the term ``manufacture'' so as to only 
include the first sentence, but is modifying the definition to include 
specified components for reasons discussed in the next section. 
Therefore, manufacture means: ``to complete the manufacturing and 
assembly processes of a product or specified component such that it is 
ready for initial sale, distribution, or operation.''
    This final rule also establishes and defines a separate term for 
``install'' to replace the term ``manufacture'' for systems assembled 
in the field. EPA discussed in the proposed rule that a field-charged 
system is ``manufactured at the point when installation of all the 
components and other parts are completed'' (emphasis added). Providing 
a separate term will reduce confusion, improve implementation, and 
allow the Agency to better address the commenters' concerns.
    Though a new term, the definition for ``install'' is substantively 
similar to the second sentence of the proposed definition of 
``manufacture.'' EPA is defining ``install'' as ``to complete a field-
assembled system's circuit, including charging with a full charge, such 
that the system can function and is ready for use for its intended 
purpose.'' As stated in the proposed rule, this definition is intended 
to address field-charged equipment beyond appliances in the RACHP 
sector to include fire suppression systems or other systems that are 
assembled and charged on-site. EPA appreciates the commenter's desire 
to harmonize State and Federal regulations where possible. However, EPA 
is not establishing definitions for ``date of manufacture'' of various 
systems in this final rule as they do not necessarily align with the 
structure of this regulation. EPA also does not find it necessary to 
specify the exact date of manufacture because compliance is determined 
by the year of manufacture. EPA discusses the adoption of other aspects 
of California's approach in section VI of this notice.
    The definition of ``install'' includes references to ``systems'' to 
distinguish equipment assembled in the field from those made in a 
factory. One commenter recommended that the Agency include a definition 
of ``appliance.'' EPA agrees with the need to distinguish field-
assembled and factory-made equipment but disagrees that using the term 
appliance is the correct approach, as it can include both factory-
charged and field-charged equipment. To better support the distinction, 
EPA is finalizing the term ``system'' and defining it as ``an 
assemblage of separate components that typically are connected and 
charged in the field with a regulated substance or substitute to 
perform a function or task.'' This new definition pertains to the 
system as a whole (e.g., supermarket or industrial process 
refrigeration (IPR)) from the components assembled into a system (e.g., 
evaporator or reach-in cooler).
4. Product, Regulated Product, Specified Components
    As with the term manufacture, EPA based the proposed definition of 
``product'' on the regulations established under title VI of the CAA in 
40 CFR part 82, subparts C and E. EPA stated in the proposed rule that 
the Agency's view of what constitutes a product for purposes of use 
restrictions under subsection (i) mirrors its meaning under those 
provisions and that using the same definition would provide clarity for 
the regulated community.
    Comment: A few commenters stated that the proposed definition of 
``product'' was too broad and would place all forms of regulated 
categories into one definition from large refrigeration equipment to 
aerosol cans containing a few ounces of propellant. Other commenters 
expressed concern about including components and subcomponents as 
examples within the definition of product. They noted that restricting 
components in the same manner as a completed product would prevent the 
manufacture or later sale of parts for normal service and warranty 
purposes. One commenter noted that the term ``product'' does not 
account for complex equipment that incorporates components using 
regulated substances (e.g., process chillers) within much larger 
equipment and requested clarification.
    Response: EPA agrees that including components within the 
definition of product, and thus the restrictions thereof, would hinder 
the manufacture and import of replacement parts intended for repairs. 
These restrictions could also unintentionally impact components that 
are capable of being used with multiple refrigerants or across multiple 
subsectors and thus are permissible in some new systems as well. EPA 
did not intend to restrict the manufacture, import, and sale of 
components in the same manner as completed products or the installation 
of new systems. EPA is therefore removing the examples of ``components 
and subcomponents'' from the final definition of ``product.'' EPA is 
also removing ``equipment'' as an example because this rulemaking uses 
that as a general term to broadly encompass items in addition to 
products (e.g., systems, components, appliances) and not as a subset.
    EPA is clarifying that the definition of ``product'' pertains to 
equipment that is completed or otherwise functional upon leaving the 
factory. This includes self-contained refrigeration and air 
conditioning appliances; foam that is blown; a manufactured item 
containing blown foam such as an appliance, car, or boat; a fully 
formulated polyol; \35\ and

[[Page 73112]]

filled aerosols. When products are incorporated into larger equipment, 
the new, larger equipment is subject to this rule. Thus, a manufactured 
item such as a refrigerator that contains insulation foam or a car that 
contains a motor vehicle air conditioner (MVAC) is subject to the 
restrictions of this rule, as are process chillers, when incorporated 
into larger equipment. The final definition of product also modifies 
the examples of fire suppression systems and foam blowing systems to 
avoid conflict with the new definition of ``system'' the Agency is 
finalizing.
---------------------------------------------------------------------------

    \35\ The Foams Technical Options Committee advising the Parties 
to the Montreal describes the term ``fully formulated polyol'' to 
mean a blend of polyols with a variety of additives such as 
catalysts, surfactants, water, flame retardants (not typically in 
appliances), including the blowing agent. UNEP, 2010. Guidance on 
the Process for Selecting Alternatives to HCFCs in Foams.
---------------------------------------------------------------------------

    EPA is defining the term ``product'' as ``an item or category of 
items manufactured from raw or recycled materials which performs a 
function or task and is functional upon completion of manufacturing. 
The term includes, but is not limited to: appliances, foams, fully 
formulated polyols, self-contained fire suppression devices, aerosols, 
pressurized dispensers, and wipes.''
    In removing components from the term ``product,'' the Agency does 
not intend to remove components from all provisions of this rule. For 
example, remote condensing units used for retail food refrigeration is 
one of the subsectors subject to a GWP limit in this rule. A single 
component may also be a major element of the entire system, such as a 
remote condensing unit for residential split system air conditioning. 
One commenter requested that EPA add a definition for ``component'' and 
clarify that it is any and all equipment required for the refrigeration 
system to function properly. The commenter suggested this would include 
but not be limited to display cases, condensing units, condensers, 
compressors, compressor rack systems, evaporator units, evaporators, 
piping, filter dryers, valves, etc.
    To allow the Agency to better describe how the restrictions apply 
to different equipment types, EPA is establishing the term ``specified 
component.'' EPA declines to finalize the definition requested by the 
commenter because it broadly describes how a component functions and 
the concept merits public input depending on the policy goals. For 
example, refrigerant piping or thermal expansion valves are components 
needed for a system to function. However, thermal expansion valves 
contain small amounts of refrigerant and operate differently from other 
components on the circuit. Refrigerant piping may not be replaced 
during a repair given it is not refrigerant specific and may be 
inaccessible. Instead, EPA is specifying components that are the major 
mechanical elements of all RACHP systems. These components tend to be 
replaced over the life of a system, are often refrigerant-specific, and 
can contain larger amounts of refrigerant when manufactured or 
imported. EPA is defining ``specified component'' as ``for purposes of 
equipment in the refrigeration, air conditioning, and heat pump sector, 
means condensing units, condensers, compressors, evaporator units, and 
evaporators.'' These components also align with those specified in 
section VI.C regarding what level of modification of a system 
effectively constitutes a ``new'' system subject to the GWP limits.
    EPA also proposed to establish a defined term, ``regulated 
product,'' that would broadly encompass all equipment that uses HFCs, 
whether they are higher-GWP HFCs that are prohibited or lower-GWP HFCs 
that are subject to labeling and reporting provisions. EPA is electing 
not to finalize this definition.
5. Retrofit
    The AIM Act defines ``retrofit'' in subsection (i)(7) as ``to 
upgrade existing equipment where the regulated substance is changed, 
which--(i) includes the conversion of equipment to achieve system 
compatibility; and (ii) may include changes in lubricants, gaskets, 
filters, driers, valves, o-rings, or equipment components for that 
purpose.'' EPA is adopting the definition contained in subsection 
(i)(7)(A) of the AIM Act with the addition of examples of equipment. 
The definition in the AIM Act is similar to but broader than EPA's 
definition of retrofit that was codified in 40 CFR part 82, subpart F. 
The AIM Act definition refers to ``regulated substance'' and 
``equipment,'' whereas the regulatory definition in 40 CFR part 82 
refers to ``refrigerant'' and ``appliances.'' As such, in this context, 
EPA finds it reasonable to interpret this term as applying not just to 
refrigeration and air-conditioning appliances, but all equipment that 
uses a regulated substance. EPA is adding a non-inclusive list of 
examples--such as air conditioning and refrigeration, fire suppression, 
and foam blowing equipment--recognizing that petitioners may seek, or 
EPA may establish, restrictions on other types of equipment using HFCs 
in the future.
    One commenter recommended that the definition of ``retrofit'' not 
be limited to just a refrigerant change as that will allow piece-meal 
system replacements without moving from a high-GWP refrigerant. The 
commenter suggested that a system be considered retrofitted after a 
threshold number of components are replaced. EPA disagrees with the 
comment that a retrofit be triggered without replacing the refrigerant 
type. As noted, the statutory definition contained in subsection 
(i)(7)(A) of the AIM Act is predicated on a change in refrigerant, and 
it reasonable to maintain this condition when the equipment uses a 
refrigerant.
6. Use
    EPA proposed to define this term as ``for any person to take any 
action with or to a regulated substance, regardless of whether the 
regulated substance is in bulk, contained within a product, or 
otherwise, except for the destruction of a regulated substance. Actions 
include, but are not limited to, the utilization, deployment, sale, 
distribution, offer for sale or distribution, discharge, incorporation, 
transformation, or other manipulation.''
    Comment: Many commenters stated that EPA's proposed definition of 
the term ``use'' is overly broad and inappropriately allows the Agency 
to regulate the sale or distribution of products. Another commenter was 
concerned that the definition could extend liability to importers and 
distributors of bulk HFCs when used in non-compliant products even 
though that is outside of their control. One commenter stated that the 
full definition of `use' is only clear in the context of the additional 
discussion in the Applicability section and recommended that elements 
of that discussion be added to the definition. Specifically, the 
commenter stated it would be useful to distinguish actions that occur 
at the market or industry level, as was intended, from the operation of 
equipment by an owner. Another commenter noted that while ``use'' is 
not synonymous with sale or distribution, ``use'' is closer to the 
point in time when a product is sold and received by the ultimate 
customer rather than the point in time when the product is manufactured 
and that EPA's restriction on the manufacture of a product bears little 
relationship to when products containing HFCs will actually be used by 
their owners.
    Response: EPA fully responds to these comments in section VI.C of 
this notice.
7. Other
    Many commenters requested EPA to establish definitions clarifying 
when an appliance is newly manufactured and/or newly installed and thus 
subject to the GWP-limits. Commenters explicitly or

[[Page 73113]]

indirectly referenced terminology used in California's regulations for 
``new refrigeration equipment,'' ``new air conditioning equipment,'' 
and ``new facility,'' as well as ``date of manufacture of self-
contained equipment'' and ``date of manufacture of remote equipment.'' 
Another commenter requested EPA define ``new'' to match the methodology 
used in New York State. EPA responds to these comments in section VI.C 
of this notice.

B. How is EPA restricting the use of HFCs in the sector or subsector in 
which they are used?

    Subsection (i) authorizes EPA to by rule restrict, fully, 
partially, or on a graduated schedule, the use of a regulated substance 
in the sector or subsector in which the regulated substance is used. 
The provision grants EPA authority to fashion restrictions on the use 
of regulated substances in the sectors that use those substances and 
does not specify a particular approach as to how restrictions must be 
structured but lists considerations EPA is to factor in, to the extent 
practicable, when promulgating restrictions. EPA is finalizing two 
approaches to structuring those restrictions, a GWP-limit and a list of 
prohibited regulated substances or blends, while recognizing that other 
approaches could be considered in the future that would also fit within 
the authority granted by this statutory provision. EPA also proposed to 
prohibit the use of all regulated substances in new products within 
particular subsectors, but some commenters noted that the Agency 
generated confusion by imprecisely describing it as a GWP-limit of 
zero. As discussed in Section VI.F.3, EPA is not finalizing an approach 
that completely prohibits the use of regulated substances in new 
products in any sector or subsector in this rulemaking and again 
maintains that the Agency has the authority to do so in a subsequent 
rulemaking.
    In establishing the two approaches contained in this final rule, 
EPA has taken into account the statutory text, feasibility, consistency 
with similar programs being implemented in the States and 
internationally, impacts on the regulated community and on innovation, 
efficiency of implementation, and other factors. Subsection (i)(4)'s 
``Factors for Determination'' provides factors that EPA is to consider 
``[i]n carrying out a rulemaking'' under subsection (i)(1). As a 
general matter, we interpret subsection (i)(1) to apply where EPA is 
deciding whether to impose a restriction on the use of a regulated 
substance in a sector or subsector and what that restriction should be 
(e.g., a full restriction or a partial restriction and on what 
timeframe). However, the factors listed in subsection (i)(4) are also 
informative in our consideration of how to structure restrictions, as 
some approaches may provide advantages with respect to some of the 
factors over others.
    Furthermore, while subsection (i)(1) identifies that EPA may 
restrict the use of a regulated substance ``in the sector or subsector 
in which the regulated substance is used,'' given EPA's authority to 
issue partial restrictions, EPA interprets this provision as allowing 
the Agency to establish restrictions for particular uses of HFCs, such 
as products or applications, and that such restrictions need not apply 
uniformly across entire sectors or subsectors. Interpreting EPA's 
authority in this manner allows the Agency to tailor restrictions in 
accordance with the best available data and to consider relevant 
differences in, for example, the availability of substitutes with 
respect to technological achievability or affordability. For example, 
EPA is establishing restrictions for HFCs used in chillers for IPR. 
However, EPA is excluding chillers for IPR with exiting fluid 
temperatures less than -58 [deg]F because lower-GWP substitutes for 
HFCs are not yet adequately technologically achievable and therefore 
not available at this time.
    The two approaches to structuring subsection (i) restrictions used 
in this rule were identified in the petitions granted by the Agency to 
date. They are either to set GWP limits for HFCs used within a sector 
or one or more subsectors or to restrict specific HFCs, whether neat or 
used in a blend, by sector or one or more subsectors.\36\ EPA is 
primarily employing the GWP limit approach in this rulemaking, with 
some exceptions where the specific-listing approach is more 
appropriate.
---------------------------------------------------------------------------

    \36\ The restrictions on the use of an HFC under subsection (i) 
of the AIM Act established in this rulemaking are intended to 
complement and not conflict with existing restrictions established 
through other authorities. Other authorities still apply.
---------------------------------------------------------------------------

    For most sectors and subsectors in this rule, EPA is establishing 
GWP limits for HFCs, whether neat or used in a blend. Under this 
approach only HFCs with GWPs below the limit or HFCs used in blends 
with GWPs below the limit may be used in that sector or subsector. If 
used neat, HFCs with GWPs at or above the GWP limit are prohibited from 
use in that sector or subsector. For HFCs used in a blend in the sector 
or subsector, compliance with the GWP limit is determined based on the 
GWP of the blend. If a blend meets two criteria (it contains an HFC and 
the GWP of the blend is at or above the GWP limit) the HFCs in the 
blend are subject to the prohibition on use, and accordingly the blend 
may not be used in that sector or subsector. References and 
descriptions of how the restrictions apply to blends throughout this 
notice incorporate this framework and have only been shortened for 
readability. A blend or other substitute that does not contain a 
regulated substance is not subject to the GWP limit.
    In general, this approach also provides a more efficient and 
streamlined process for companies to employ lower-GWP substitutes for 
new uses, because the existing restrictions make clear what substitutes 
are permissible. In contrast, promulgating restrictions under 
subsection (i) using only a substance-specific listing approach could 
create hesitancy to innovate because it would be less clear whether EPA 
might restrict a particular blend containing an HFC after a company had 
already invested resources in developing it for a particular use.
    To determine the GWP of a blend that uses an HFC, all components of 
the blend are incorporated, whether an HFC, HFO, hydrocarbon or other 
constituent, using the 100-year integrated AR4 values.\37\ We note that 
the 100-year integrated GWP values in Table 2.15 of AR4 for the HFCs 
are equivalent to the exchange values listed in the AIM Act and thus 
what we plan to use here without change. Further details about 
determining the GWP of compounds that are not listed in AR4 are found 
in section IV.A of this preamble.
---------------------------------------------------------------------------

    \37\ This rule does not change in any way the calculation 
established under 40 CFR part 84, subpart A for determining the 
quantity of production and consumption allowances required for 
regulated substances used in blends.
---------------------------------------------------------------------------

    For refrigerants, the blend includes the components in amounts as a 
weight percentage, consistent with the refrigerant designation in 
ASHRAE Standard 34, ``Refrigerant Designations and Safety 
Classifications'' or the SNAP listing. The refrigerant blend considered 
in the GWP calculation does not include other additives such as 
compressor oil or stabilizers. For foams, the blend includes components 
that are part of the blowing agent as a weight percentage. The blowing 
agent blend considered in the GWP calculation does not include other 
parts of the foam formulation such as plastic resin, catalysts, flame 
retardants, or stabilizers. In general, aerosols do not use blends as 
propellants, but multiple HFCs may be used together in an aerosol 
solvent

[[Page 73114]]

blend, in which case the blend would include the component solvents and 
propellants in amounts as a weight percentage. Other parts of the 
aerosol formulation are not considered in calculating the aerosol's 
GWP, such as water, fragrances, emulsifiers, pigments, anti-bacterial 
agents, pesticides, or polymers.
    In most cases it is the specific HFC and the proportion of that HFC 
within the blend that determines the GWP of the blend as a whole. EPA 
is not restricting the use of any specific HFC when used in blends. For 
instance, for sectors or subsectors with a GWP limit of 150, HFC-134a 
neat, which has a GWP of 1,430, cannot be used, while R-451A, which is 
a blend of HFC-134a and HFO-1234yf, has a GWP of 147 and may be used. 
In other words, an HFC with a GWP above the limit may continue to be 
used when it is used in a blend, such that the total GWP of the blend 
is below the limit. There may be certain characteristics associated 
with a higher-GWP HFC that make use of that substance in a blend 
particularly advantageous, and in some cases increase the availability 
of that substitute for use, such as improving safety by reducing 
flammability. The GWP limit approach, which allows for the continued 
use of certain higher-GWP substances in blends, rather than strictly 
prohibiting the use of those higher-GWP substances in a sector or 
subsector, can smooth the glide path to transition, support innovation, 
and achieve beneficial environmental impacts sooner than waiting for 
the development of a substitute that contains no amount of a higher-GWP 
regulated substance.
    Comment: Multiple commenters, including those representing users of 
regulated substances across different sectors, agreed that establishing 
GWP limits provides regulatory certainty and encourages the continued 
development and implementation of HFC substitutes with lower GWPs. A 
few commenters agreed that using a similar approach allows for 
harmonization across jurisdictions. Commenters also noted that using 
GWP limits is easy for downstream equipment users to understand, easier 
for the Agency to implement, and provides flexibility. One commenter 
supported GWP limits as it more clearly articulates EPA's intention to 
reduce the warming impact of HFCs and that it provides a more 
straightforward way for EPA to tighten restrictions by ratcheting down 
the GWP limits in the future.
    One commenter strongly favored the specific-listing approach over 
the GWP limit approach. The commenter stated that the GWP limit 
approach poses huge noncompliance issues and dangers to users of 
products containing regulated substances by shifting the obligation to 
assess the safety of a substitute to the end-user. The commenter noted 
that the basis for their concern is that the Agency would no longer 
update SNAP listings. The commenter also recognized the downsides of a 
specific-listing approach but still found specific-listing to be 
preferable if the GWP approach meant the Agency was not assessing the 
risks associated with substitutes.
    Response: EPA acknowledges the broad support for using GWP limits 
as the method for restricting the use of certain HFCs by sector or 
subsector and for the reasons discussed in the proposed rule is 
primarily using that approach in this final rule. Additionally, the GWP 
listing approach is not a replacement for SNAP listings or reviews of 
environmental, health, and safety impacts. Congress provided separate 
authority under subsection (i)(5) of the AIM Act for EPA to evaluate 
substitutes for HFCs in a sector or subsector, taking into account 
technological achievability, commercial demands, safety, overall 
economic costs and environmental impacts, and to make the evaluation 
public, including the factors associated with the safety of those 
substitutes. EPA intends to continue providing information on its 
evaluation of alternatives to HFCs.
    Furthermore, contrary to commenter's suggestion, EPA continues to 
promulgate rules under SNAP. Section 612(c) of the CAA requires EPA to 
promulgate rules making it unlawful to replace ODS with any substitute 
that it determines may present adverse effects to human health or the 
environment where it has identified an alternative that (1) reduces the 
overall risk to human health and the environment and (2) is currently 
or potentially available. Section 612(c) further requires EPA to 
``publish a list of (A) the substitutes prohibited under this 
subsection for specific uses and (B) the safe alternatives identified 
under this subsection for particular specific uses.'' Under SNAP, EPA 
evaluates substances that can be used as alternatives based on multiple 
criteria and accordingly lists them as acceptable, unacceptable, 
acceptable subject to use conditions, acceptable subject to narrowed 
use limits, or pending. See 40 CFR 82.180(a)(7) (listing criteria for 
review) and 40 CFR 82.180(b) (describing types of listing decisions). 
EPA has considered more than 500 alternatives for eight industry 
sectors and more than 40 end uses since 1994.\38\ EPA will continue to 
evaluate alternatives in the sectors and subsectors where ozone-
depleting substances have been and are being used.\39\ EPA recently 
finalized SNAP Rule 25 listing lower-GWP alternatives as acceptable, 
subject to use conditions, for chillers-comfort cooling, residential 
dehumidifiers, residential and light commercial air conditioning and 
heat pumps. SNAP Rule 25 also listed ethylene as acceptable, subject to 
use conditions and narrowed use limits, in very low temperature 
refrigeration. (88 FR 26382; April 28, 2023). EPA also recently 
proposed SNAP Rule 26 which would list lower-GWP alternatives as 
acceptable, subject to use conditions, for retail food refrigeration, 
commercial ice machines, IPR, cold storage warehouses, and ice-skating 
rinks. (88 FR 33722, May 24, 2023). As discussed in section VI.E.2 of 
this preamble and the American Innovation and Manufacturing Act of 
2020--Subsection (i)(4) Factors for Determination: Safety, referred to 
in this preamble as the ``Safety TSD,'' assessments of safety and other 
characteristics under SNAP are duly considered in our examination of 
availability (as it relates to safety and other factors) under AIM Act 
subsection (i)(4)(B).
---------------------------------------------------------------------------

    \38\ As noted in section VI.A of this preamble, there is 
significant overlap between the sectors and subsectors identified in 
this proposal and how sectors and ``end-uses'' are categorized under 
the SNAP program.
    \39\ After a court challenge, the D.C. Circuit partially vacated 
SNAP Rule 20 (80 FR 42870, July 20, 2015) ``to the extent it 
requires manufacturers to replace HFCs with a substitute 
substance,'' and remanded to EPA for further proceedings. Mexichem 
Fluor, Inc. v. EPA, 866 F.3d 451, 464 (D.C. Cir. 2017) (``Mexichem 
I''). However, the court upheld EPA's decisions in that rule to 
change the listings for certain HFCs in certain SNAP end-uses from 
acceptable to unacceptable as being reasonable and not arbitrary and 
capricious. Id. at 462-64. The same court later issued a similar 
partial vacatur for portions of the SNAP Rule 21 (81 FR 86778, 
December 1, 2016). See Mexichem Fluor, Inc. v. EPA, 760 Fed. Appx. 6 
(Mem) (per curiam) (D.C. Cir. 2019) (``Mexichem II'').
---------------------------------------------------------------------------

    Therefore, EPA is primarily finalizing the use restrictions in this 
action by employing a GWP limit approach because this approach supports 
innovation, transition, and compliance. Furthermore, for the reasons 
discussed in the proposed rule and based on the comments received, EPA 
is in most instances not employing a specific listing approach in its 
use restrictions, except in limited circumstances. For example, we find 
the specific listing approach can be preferable where the subsector has 
not yet identified favored lower-GWP substitutes to transition to, but 
is in a position, per subsection (i)(4), to transition away from using 
the highest-GWP regulated substances. It

[[Page 73115]]

allows additional time before establishing a GWP limit (which, to serve 
regulatory certainty and innovation, the Agency would prefer not to 
repeatedly revisit) while still restricting those substances that have 
the highest environmental impact. This approach would allow for the 
adoption of multiple transitional substitutes and allow for the 
development of additional substitutes before issuing a GWP-limit-based 
restriction. As such, EPA is using both approaches in combination, with 
some subsectors having a GWP limit and others where specific substances 
are restricted.

C. Applicability

    HFCs are used in a wide variety of sectors, including refrigeration 
and air conditioning, foams, aerosols, and fire suppression. In these 
sectors, HFCs are used as a refrigerant, foam-blowing agent, solvent, 
propellant, and fire suppression agent and may be contained within or 
emitted from equipment such as a product or system. HFCs are also used 
in processes such as semiconductor manufacturing and chemical 
manufacturing. Subsection (i) of the AIM Act provides that the 
Administrator may by rule restrict, fully, partially, or on a graduated 
schedule, the use of a regulated substance in the sector or subsector 
in which the regulated substance is used. EPA interprets its authority 
under subsection (i) to cover a broad chain of sector and subsector 
activities associated with equipment that uses regulated substances.
    EPA designed the restrictions of this rule to apply at certain 
points in this chain of activities, consistent with the Act's direction 
that EPA ``may by rule restrict, fully, partially, or on a graduated 
schedule.'' In light of the fact that the restrictions in this final 
action are the first to be issued under subsection (i), EPA views 
restrictions on the incorporation of higher-GWP HFCs into new products 
and systems and on the introduction and circulation of those products 
in the market as the most efficient and effective way to encourage a 
subsector to transition from the use of those HFCs. This rule therefore 
(1) restricts the use of HFCs in the manufacture and import of new 
products; (2) restricts the subsequent sale or distribution, offer for 
sale and distribution, purchase or receipt for sale or distribution, or 
export of those products; and (3) restricts the installation of new 
systems and the significant modification of existing systems.
    In general, these restrictions apply primarily to original 
equipment manufacturers (OEMs) and importers, as these are the entities 
that introduce such products and components of such systems into the 
U.S. market. The restrictions in this rule that apply to distributors 
(including online platforms), retailers, and exporters are intended to 
reinforce the manufacture and import restrictions, and to ensure that 
incentives throughout the market chain are aligned toward transitioning 
a subsector from regulated substances where available substitutes 
exist. Entities that install new systems, including those that 
assemble, contract for, or take possession of the system are also 
subject to these restrictions.
    EPA is cognizant of the continued need in the covered sectors and 
subsectors for components to service and maintain existing systems that 
use higher-GWP HFCs. This rule therefore allows for the continued 
manufacture, import, sale, distribution, and export of components, 
subject to labeling, reporting, and recordkeeping requirements. EPA is 
generally not applying restrictions on the use of HFCs in existing 
products or systems or used products, except, for example, in limited 
circumstances such as the import of used products or modification of a 
system to the point that it constitutes replacement (see section VI.C.3 
of the preamble). To that end, this rule does not restrict the use of 
HFCs in ordinary repair and servicing of products or systems, nor is 
EPA applying the restrictions to the use of HFCs in retrofit 
applications.
1. What is EPA's statutory authority for this action?
Summary of the Proposed Rule
    Subsection (i) grants EPA authority to restrict the use of a 
regulated substance in the sector or subsector in which the regulated 
substance is used, and the Act does not define ``use.'' For several 
reasons, summarized below, EPA proposed to define ``use'' in the 
context of subsection (i) as including actions taken with respect to 
regulated substances that occur at the market or industry level, such 
as manufacture, distribution, sale, and offer for sale--i.e., to cover 
the presence of HFCs in products and processes in the U.S. market--as a 
way of addressing their use in sectors and subsectors. EPA's 
interpretation of its authority under this section is grounded in the 
statutory text and purposes.
    First, sectors and subsectors are not defined in the AIM Act, but 
those terms suggest groupings or categories of related activity at an 
industry level. EPA is defining ``sectors'' and ``subsectors'' 
consistent with historical usage of those terms in other programs--
grouping together similar or related industrial or market uses into 
distinct sectors; for example, refrigeration and air conditioning, 
foams, or aerosols. The AIM Act language, ``use of a regulated 
substance in the sector or subsector in which the regulated substance 
is used,'' makes plain that the grant of authority under subsection (i) 
was intended to cover a sector or subsector's use of a regulated 
substance. The inclusion of a regulated substance in a product \40\ or 
system to achieve a particular purpose--e.g., using an HFC as a 
refrigerant in a refrigerator or in an air conditioner--is a 
prototypical use for sectors in which regulated substances are used.
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    \40\ Similarly, subsection (i)'s authority extends to regulated 
substances contained in a blend and the use of that regulated 
substance within a blend by the sector or subsector in a product or 
process to achieve a particular purpose. To address the regulated 
substance within a blend, it is appropriate to establish 
requirements that apply to use of the blend, although the blend 
itself is not a regulated substance.
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    Second, because subsection (i) and the subsection (i)(4) factors 
are focused on broad, sector-level information, we proposed that it is 
reasonable to interpret ``use'' broadly, in a way that would reach uses 
on a sector-level basis. The subsection is titled ``Technology 
Transitions,'' and in subsection (i)(4), the Act directs EPA to 
consider certain factors, to the extent practicable, in issuing a 
rulemaking or making a determination to grant or deny a petition 
regarding use restrictions. The factors listed under subsection (i)(4) 
task the Agency with examining information relevant to industry-level 
sectors or subsectors that would inform consideration of the 
feasibility and advisability of establishing requirements for a 
transition away from the use of a regulated substance in that sector or 
subsector, as well as consideration of whether that transition should 
be full, partial, or on a graduated schedule. For example, subsection 
(i)(4)(B) directs EPA to factor in ``the availability of substitutes 
for use of the regulated substance that is the subject of the 
rulemaking or petition, as applicable, in a sector or subsector, taking 
into account technological achievability, commercial demands, safety, 
consumer costs, building codes, appliance efficiency standards, 
contractor training costs, and other relevant factors, including 
quantities of regulated substances available from reclaiming, prior 
production, or prior import.'' The various subfactors in (i)(4)(B) help 
EPA to determine whether there are adequate available substitutes for a 
regulated

[[Page 73116]]

substance that a sector or subsector could use, indicating feasibility, 
readiness, advisability, and degree of a sector or subsector's 
transition away from the regulated substances in use. Similarly, the 
other factors in (i)(4)--to use best available data, to consider 
overall economic costs and environmental impacts as compared to 
historical trends, and to consider the remaining phasedown period for 
regulated substances under the phasedown rule issued under subsection 
(e), if applicable--also fit with this understanding of EPA's task: to 
determine whether, when, and to what degree it is appropriate to 
establish a use restriction to facilitate the transition of a sector or 
subsector from the use of regulated substances.
    Third, we explained in the proposed rule that Congress provided EPA 
authority to issue restrictions that are full, partial, or on a 
graduated schedule. Fully restricting the use of a regulated substance 
in the sector or subsector in which it is used, by its terms, implies a 
full transition away from the use of that regulated substance in the 
given sector or subsector. We therefore understand EPA's ability to 
restrict ``use of a regulated substance in the sector or subsector in 
which it is used'' to be broad enough to achieve a full transition such 
that the regulated substance would no longer be present in any portion 
of the sector or subsector. To effectuate a full transition, we would 
have to be able to address all the aspects where the regulated 
substance is present in that sector or subsector of the market. There 
may be situations where a restriction is best targeted at points in the 
life cycle or market chain of the regulated substance that are 
subsequent to the incorporation of the regulated substance in a product 
or process, as well as points in the chain that are proximate to 
ultimate use. Thus, we interpret the term ``use,'' and EPA's authority 
under AIM Act subsection (i), as being broad enough to reach points 
such as transport or offer for sale.
    EPA therefore proposed to interpret use of a regulated substance in 
the sector or subsector for purposes of subsection (i) as ``for any 
person to take any action with or to a regulated substance, regardless 
of whether the regulated substance is in bulk, contained within a 
product, or otherwise, except for the destruction of a regulated 
substance. Actions include, but are not limited to, the utilization, 
deployment, sale, distribution, discharge, incorporation, 
transformation, or other manipulation.'' EPA's proposed definition of 
``use'' therefore covered all of the links on the chain representing 
how regulated substances are introduced, incorporated into products or 
processes, circulated, and made available in the U.S. market.
    We explained in the proposed rule that even though the Act grants 
EPA broad authority to achieve a full transition from regulated 
substances in a sector or subsector, there are many actions not 
included within the scope of the restrictions covered by this final 
rule, including actions associated with steps in the disposal chain 
such as recovery, recycling, and reclamation of a regulated substance; 
the ordinary utilization or operation of a system or product by a 
consumer; \41\ and the six specific applications with a current 
qualification for application-specific allowances under 40 CFR 84.13. 
As explained in the proposed rule, given that we are at the outset of 
the phasedown of regulated substances, the restrictions in this action 
are aimed at limiting the introduction of new products that use 
regulated substances to the market and restricting the circulation of 
those products (e.g., sale or distribution) before they reach the 
consumer. In that vein, the final rule includes ``offer for 
distribution'' in addition to offer for sale in the definition of use. 
Similarly, we proposed to restrict the installation of new systems 
using HFCs under the proposal by defining manufacture to include the 
installation of new systems. EPA is finalizing its definition of 
``use'' under subsection (i), with these clarifications, consistent 
with the interpretation of ``use in the sector or subsector in which 
the regulated substance is used'' articulated in the proposed rule and 
described above.
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    \41\ Noting, however, that in some cases the consumer may have 
purchased a product where the first incorporation of the regulated 
substance occurs when the product is in the consumer's ownership, 
and in those cases that incorporation would be covered by the 
requirements.
---------------------------------------------------------------------------

    Comment: Most of the comments the Agency received in response to 
its proposed interpretation of EPA's scope of authority under 
subsection (i) and of EPA's definition of ``use of the regulated 
substance in the sector or subsector in which the regulated substance 
is used'' related to the proposed prohibition on the sale, 
distribution, and offer for sale or distribution of many regulated 
products that would go into effect on January 1, 2026 (i.e., the sell-
through period). Many commenters objected based on their view of the 
practical consequences of a one-year sell-through period, raising 
concerns about the economic harm of stranded inventory, and in 
particular, the high likelihood of stranded seasonal inventory such as 
air conditioners. Others commented on the difficulties of implementing 
any prohibition on the sale of parts of equipment that contain 
regulated substances, where those parts would continue to be needed for 
servicing and repair of existing equipment. Another commenter argued 
that prohibiting the sale of any inventory that was not sold by the 
sell-through prohibition date would constitute a ``taking'' without 
just compensation under the U.S. Constitution. These comments are 
summarized and addressed in section VI.C.2.c of this preamble.
    A smaller subset of commenters alleged that EPA lacked statutory 
authority to promulgate a sell-through limitation under the AIM Act. 
One commenter claimed that the AIM Act only provides EPA with authority 
to prohibit the ``manufacture'' of high-GWP equipment, and that had 
Congress intended to allow EPA to have broader authority to regulate 
under subsection (i), it would have employed the same language that is 
used in subsection (h) of the AIM Act, which uses the terms ``any 
practice, process, or activity.'' This commenter claimed that the 
Agency had relied upon dictionary definitions of the word ``use'' and 
that other dictionary definitions supported the commenter's preferred 
interpretation of that word to be limited to acts or practices that 
``employ, use, or put a regulated substance into service,'' and noted 
that at least one dictionary definition indicated that ``use'' means 
``long-continued possession and employment of a thing for the purpose 
for which it is adapted.'' The commenter therefore asserted that the 
Agency's regulatory definition should not include sale or distribution, 
since in the commenter's view, neither action is the act or practice of 
employing, using, or putting a regulated substance into service, nor is 
sale or distribution ``the long-continued possession'' and ``employment 
for the purpose for which it is adapted,'' which, the commenter stated 
in the case of RACHP, is the transfer of heat.
    Specifically, the commenter urged EPA to adopt the following 
definition of ``use'' under subsection (i): ``Use means the act or 
practice of employing a product containing or designed to contain a 
regulated substance. Use does not include the destruction of a 
regulated substance.'' The commenter argued that its proffered 
definition would still allow EPA to phase out the manufacture of 
products made of or containing regulated substances without going 
beyond, in its view, the authority of the AIM Act. Further, the 
commenter claimed that a sell-through limitation, rather than a 
regulation based only on

[[Page 73117]]

a product's date of manufacture, would be ``unique'' in comparison to 
numerous other regulations on durable goods, including those 
promulgated by the U.S. Department of Energy (DOE).
    Response: We disagree with commenters who allege that EPA does not 
have authority under subsection (i) of the AIM Act to issue 
restrictions on the sale or distribution of products that use regulated 
substances. We do not agree with the commenter's reading of the 
statute, and specifically, its views that subsection (i) the AIM Act 
only provides EPA with authority to prohibit the ``manufacture'' of 
higher-GWP equipment and that, in contrast to subsection (h), which 
uses the language of ``any practice, process, or activity,'' EPA's 
authority under subsection (i) is comparatively limited. In fact, 
subsection (i) does not mention either manufacture or equipment, much 
less contain any limitation that EPA may only address manufacture of 
equipment under subsection (i). Subsection (i)(1) says, with respect to 
EPA's authority, that ``[s]ubject to the provisions of this subsection, 
the Administrator may by rule restrict, fully, partially, or on a 
graduated schedule, the use of a regulated substance in the sector or 
subsector in which the regulated substance is used.'' There is nothing 
in this provision that suggests that EPA's statutory authority under 
(i) is limited to issuing restrictions on manufacturing, nor does the 
provision suggest that only higher-GWP equipment may be the target of 
EPA's restrictions. To the contrary, this language broadly authorizes 
EPA to restrict any use of a regulated substance in the sector or 
subsector in which the regulated substance is used; there is no 
limitation, express or implied, to certain types of use or users.\42\ 
These are assumptions that the commenter appears to have made without 
any grounding in the text of the statute.
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    \42\ Congress included express limitations on the applicability 
of the rules under AIM subsection (i) in a later part of the 
subsection (see subsection (i)(7)), and neither of the limitations 
in that provision mention a limitation to the manufacture of higher 
GWP equipment. Had Congress intended the kind of restriction the 
commenters suggest, it is reasonable to think they would have 
included those restrictions in subsection (i)(7).
---------------------------------------------------------------------------

    We also do not agree with the commenter's view that Congress' 
decision to use different language than it did for subsection (h) 
(i.e., its omission of the terms ``any practice, process, or 
activity,'' which appear in subsection (h)) somehow narrows the scope 
of subsection (i). The commenter appears to ignore the full context of 
each provision. Subsection (h) and subsection (i) use different 
language and are framed differently, but that does not mean that one is 
narrower or the other broader. Rather, EPA interprets those differences 
as conveying authority that is tailored to the respective area of focus 
of these subsections so that EPA can establish regulatory regimes that 
effectively achieve their respective purposes and complement one 
another. Because EPA is establishing these provisions under subsection 
(i), the critical question is whether they are within the authority 
conveyed under subsection (i) as Congress drafted it, not whether they 
would be authorized under some other language. When the statutory text 
of subsection (i) is read in full context, it comfortably encompasses 
restrictions on a range of entities that use regulated substances, not 
just manufacturers of equipment. One authority EPA has under (i) can be 
stated as follows: ``[t]he Administrator may . . . restrict fully . . . 
the use of a regulated substance in the sector or subsector in which 
the regulated substance is used.''
    Subsection (i)'s grant of authority to issue a full restriction 
across use in a sector or subsector was a key rationale underlying 
EPA's interpretation. As EPA pointed out at proposal, EPA interprets 
the statute in a way that could give meaning to subsection (i)'s grant 
of authority to effectuate a full restriction, and thus transition, of 
all uses of a regulated substance in any given sector or subsector. As 
we explained in the proposed rule, a narrower interpretation of EPA's 
authority to exclude sale or distribution could circumvent the intended 
full transition of a sector or subsector away from use of HFCs. 
Consistent with these concerns articulated in the proposed rule, EPA 
received a comment from a State that has restricted the manufacture of 
products containing HFCs without a sell-through limitation, and that 
State observed that such an ``approach can create challenges as it 
relies on regulated entities to provide documentation as to manufacture 
date,'' and that ``[n]ot all entities in the market chain can provide 
such information for all products,'' noting that ``[t]hese factors are 
further complicated when applied to international manufacturers and 
retailers.'' These concerns lend further support to EPA's view that 
covering all points in the market chain of ``use in the sector or 
subsector'' ensures that the use restrictions we establish achieve 
their intended purpose, where the intention is to fully restrict the 
use of a regulated substance in a sector or subsector, or, as in this 
case, to partially restrict the use of regulated substances before 
those substances reach consumers. As discussed in the proposed rule, 
even though EPA's definition of ``use'' is broad in order to enable the 
Agency to fully exercise the subsection (i) authority under that 
provision and to facilitate a full transition to HFC substitutes where 
appropriate, that does not mean that in every instance the restrictions 
promulgated under subsection (i) will exercise that full authority. In 
many cases, as in this action, EPA may issue partial restrictions that 
target only certain uses.
    The same commenter who asserted EPA has no authority to restrict 
sale or distribution provided no rebuttal or engagement with the 
reasoning EPA provided at proposal for its interpretation: namely, that 
the express provision of subsection (i) is related to a sector or 
subsector's use of a regulated substance, that the subsection (i)(4) 
factors require EPA to analyze information related to a restriction's 
feasibility and impact from a sector-level viewpoint, and that, as 
stated previously, the authority to ``restrict fully'' means that EPA 
has authority to restrict many activities in a sector- or subsector-
level chain where regulated substances are present, and therefore 
``used'' in that sector or subsector. Instead, the commenter claimed 
that EPA ``justified'' its interpretation by relying on dictionary 
definitions of the word ``use.'' This is not accurate. We began the 
proposed rule's preamble discussion with citations to the dictionary 
definition of that word, but the reasoning for our proposed 
interpretation and definition of the term did not rest solely on the 
dictionary definitions.
    Nor do we agree with the commenter that their proffered definition, 
which relies on the commenter's ``dictionary definition'' understanding 
of the term ``use,'' is workable. The commenter suggests that EPA 
should define ``use'' as ``the act or practice of employing a product 
containing or designed to contain a regulated substance. Use does not 
include the destruction of a regulated substance.'' We do not agree 
with commenter's assertion that this definition ``would still allow EPA 
to phase out the production of products made of or containing regulated 
substances.'' Putting aside the commenters' confusing use of the term 
``phase out'' in the context of subsection (i), which addresses use 
restrictions, under the commenter's definition, EPA would only be 
allowed to restrict the act or practice of employing a product 
containing or designed to contain a

[[Page 73118]]

regulated substance. We fail to see how this definition of use would 
allow EPA to restrict the manufacture of products containing HFCs, 
because the creation of a product is not the act or practice of 
employing that product, nor would EPA be permitted to restrict the 
import of such products, because import also does not ``employ'' the 
product. In fact, under the commenter's suggested definition, it would 
appear that the only potential regulated parties under AIM Act 
subsection (i) would be the consumers of products, as these are likely 
the only parties that would be ``employing'' the products, as the 
commenters seem to be using that term, and for the sector the commenter 
represents (RACHP), the consumers are almost certainly the only parties 
that are ``employing'' the products for ``the purpose for which it is 
adapted, i.e., the transfer of heat'' (to quote the commenter's 
understanding of and application of the dictionary definition of 
``use''). We disagree that this is a reasonable reading of the AIM Act, 
given the textual considerations that subsection (i)(4) sets the Agency 
to consider when determining whether or not to restrict the ``use of a 
regulated substance in the sector or subsector in which the substance 
is used.'' (emphasis added).
    We also note that despite the commenter's observation that many 
regulations on goods, including those promulgated by the U.S. DOE, 
establish compliance based only on manufacture, that has little 
relevance for EPA's interpretation of the term ``use'' in subsection 
(i). EPA's action is governed by the authority grounded in the text of 
the AIM Act, not the text of the statute providing DOE authority to 
promulgate its regulations. In any case, designing a restriction that 
regulates actions other than manufacture is not ``unique.'' In the 
context of SNAP under CAA section 612, which evaluates alternatives to 
ozone-depleting substances like chlorofluorocarbons (CFCs) (class I 
substances) and HCFCs (class II substances), EPA has long defined 
``use'' as ``any use of a substitute for a class I or class II ozone-
depleting compound, including but not limited to use in a manufacturing 
process or product, in consumption by the end-user, or in intermediate 
uses, such as formulation or packaging for other subsequent uses.'' 40 
CFR 82.172. The Agency's interpretation of the scope of its authority 
and its definition of the term ``use'' in the subsection (i) context 
similarly conceives of this authority as including the introduction of 
products containing regulated substances into what we consider to be 
sector or subsector activity, and the full market chain of activities, 
or ``intermediate uses,'' that follow, through to the consumer or end-
user.
2. What uses is EPA restricting in this rule?
a. Manufacture and Import of Factory-Completed Products
    This rule includes restrictions that apply to the manufacture of 
certain factory-completed products by the dates specified in section 
VI.F. As discussed in section VI.A on definitions, commenters were 
generally supportive of EPA's proposal to establish use restrictions on 
the manufacture of factory-completed products using regulated 
substances. Many of the comments received on EPA's proposal to restrict 
manufacturing related to EPA's proposed definition of ``manufacture'' 
to include the installation of field-assembled systems.
    EPA proposed to apply its restrictions equally as to domestically 
manufactured products using HFCs and products using HFCs that are 
imported. The AIM Act defines ``import'' as ``to land on, bring into, 
or introduce into, or attempt to land on, bring into, or introduce 
into, any place subject to the jurisdiction of the United States, 
regardless of whether that landing, bringing, or introduction 
constitutes an importation within the meaning of the customs laws of 
the United States,'' and this rule follows that definition. Commenters 
were supportive of EPA's equal application of the proposed restriction 
to the manufacture of products using HFCs and to the import of products 
using HFCs, noting that restricting both manufacture and import would 
garner environmental benefits, meet industry expectations, and treat 
all equipment equally regardless of location of manufacture and 
availability of HFCs under the global phasedown. EPA is finalizing the 
restriction on the import of products as proposed.
    While EPA is generally not regulating used equipment (see section 
VI.C.b), the Agency proposed to restrict the import of all products 
that do not meet the GWP limits, regardless of when the product was 
manufactured and regardless of whether the product is used. The goal of 
restricting the use of regulated substances (in this case, higher-GWP 
HFCs) in the named sectors and subsectors would be undermined if those 
sectors and subsectors could simply shift use to imported products 
containing higher-GWP HFCs that were not subject to the Agency's 
restrictions.
    AIM Act subsection (i)(7)(B)(ii) states that subsection (i) rules 
shall not apply ``except for a retrofit application, [to] equipment in 
existence in a sector or subsector before December 27, 2020.'' EPA 
interprets this limitation with respect to ``equipment in existence in 
a sector or subsector'' not to apply to equipment manufactured abroad 
prior to the Act's date of enactment, because EPA interprets ``sector 
or subsector'' in that provision to mean a sector or subsector in the 
United States. In general, where those terms appear in subsection (i) 
of the AIM Act, EPA understands them to mean the domestic sector or 
subsector, not the sector or subsector as it exists, operates, and 
functions in another country. For example, in assessing the 
availability of substitutes for use in a sector or subsector under 
subsection (i)(4)(B), EPA is generally analyzing the various 
subfactors--consumer costs, building codes, appliance efficiency 
standards, contractor training costs--vis-[agrave]-vis the domestic 
impacted sector or subsector.\43\ Therefore, equipment that was 
manufactured in another country and existed prior to December 27, 2020, 
but was not imported to the United States until after that date is not 
subject to subsection (i)(7)(B)'s limitation, because until it is 
imported into the United States, it is not ``in existence in the sector 
or subsector.''
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    \43\ EPA is examining international information for some of the 
analyses, such as research from international organizations about 
technological achievability, because such information has relevance 
for the sector or subsector in the United States.
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    EPA received a number of comments related to its application of 
restrictions on imports, and we summarize and respond to these comments 
below.
    Comment: One commenter supported and one commenter opposed the 
proposal to restrict the import of products not meeting the GWP limits, 
regardless of when the product was manufactured and regardless of 
whether the products are used. The commenter opposed to EPA's proposal 
requested that EPA clarify that ``equipment in existence as of December 
27, 2020'' applies to all equipment in existence up to the date of this 
rule's proposal, wherever that equipment is located (i.e., whether in 
the United States or elsewhere), at least for semiconductor 
manufacturing equipment. The commenter asserted that semiconductor 
manufacturers have been producing semiconductor manufacturing equipment 
in the last two years that was designed well before the AIM Act was 
enacted, and that such equipment was intended to operate for the next 
10 to 25 years. The commenter argues that until EPA published its 
proposed rule,

[[Page 73119]]

semiconductor manufacturers did not have ``actionable notice'' that 
their products might be subject to the Agency's restrictions. The 
commenter also states that complex semiconductor manufacturing 
equipment may have been manufactured outside of the United States but 
was intended for use in the U.S. semiconductor sector. The commenter 
noted that the semiconductor industry has a global supply chain with 
long production timelines and asserted that EPA's proposed distinctions 
based on where equipment is located could impose significant 
complications on the sector's supply chain management.
    Response: The Act's exception from applicability in AIM Act 
subsection (i)(7)(B)(ii) plainly does not apply to any equipment 
manufactured after December 27, 2020. We therefore do not agree with 
the commenter that the exception in that provision could be interpreted 
to apply to equipment manufactured between the date of the AIM Act's 
enactment and the publication of EPA's proposed rule. The statute is 
clear on its face, whether or not regulated entities were aware of 
being potentially subject to regulation under these provisions of the 
AIM Act until EPA issued its proposed rule.
    We also clarify that not all equipment that uses regulated 
substances in the semiconductor manufacturing industry is subject to 
these rules. The use of regulated substances in many semiconductor 
manufacturing processes, such as etching and the use of HFCs as 
solvents, is not restricted by this final action. EPA's restrictions 
cover only the use of HFCs as they relate to semiconductor 
manufacturing where those HFCs are used as a refrigerant in chillers 
for IPR. As discussed in section VI.F.1.j, EPA is differentiating its 
restrictions and the timing of those restrictions for this subsector 
based on the temperature of the exiting fluid. To the extent that the 
equipment cited by commenter has exiting fluid temperatures below -50 
[deg]C (-58 [deg]F), the import of such new equipment is not restricted 
by this rule. For equipment with exiting fluid temperatures above that 
temperature, EPA has delayed the compliance date for installations of 
new systems to either 2026 or 2028 (again differentiating based on the 
temperature of the exiting fluid). Importing components of such systems 
may continue after those compliance dates to allow servicing of 
existing equipment in the U.S.
    Comment: One commenter opposed to EPA's proposal to apply its 
restrictions to all imported products using HFCs above the GWP limits 
requested that used semiconductor manufacturing and related equipment 
(SMRE) that was designed to contain HFCs receive an exemption. The 
commenter stated that there is a robust and active market for used 
SMRE, and preventing the import of this used equipment could have 
inadvertent supply chain disruption effects.
    Response: EPA understands the semiconductor manufacturing equipment 
to fit within the IPR subsector, typically utilizing chillers, often 
built into other non-refrigerant containing equipment, to cool 
processes necessary to produce semiconductor chips and other 
electronics. As such, we do not view such equipment differently from 
other IPR systems, which likewise could conceivably integrate a chiller 
into other equipment (e.g., a chiller integrated with a conveyor belt 
intended to move food needing freezing along its production process). 
As discussed in section VI.F.1.j, EPA is finalizing a compliance date 
later than proposed based on our consideration of the subsection (i)(4) 
factors. Specifically, EPA is establishing a compliance date of January 
1, 2028, for IPR chillers where the fluid exiting the chiller is below 
-22 [deg]F (-30 [deg]C), and a January 1, 2026, date for other such 
equipment. And, consistent with the proposed rule, this final rule does 
not restrict HFC use in such equipment where the fluid exiting the 
chiller is below -50 [deg]C (-58 [deg]F). This additional time compared 
to the proposal should assist in the commenter's ability to respond to 
the restrictions in this rule; for example, by importing appropriate 
equipment prior to the relevant compliance date and/or altering 
manufacturing outside the United States to use refrigerants that meet 
the restrictions for the United States (i.e., less than 700 GWP).
    Comment: Other commenters asked that EPA clarify how the import 
restriction applies to existing intermodal containers that are engaged 
in trade, refrigeration equipment in operation on ocean-going vessels, 
and non-road motor vehicles temporarily deployed overseas. Commenters 
stated that applying the GWP limit to all refrigerated containers is 
infeasible and would be highly disruptive to trade. Commenters also 
stated that such equipment should be allowed to be serviced in the 
United States and not be subject to the recordkeeping and reporting 
requirements.
    Response: EPA agrees that applying the restrictions to products 
that are actively in use when travelling into U.S. jurisdiction could 
be problematic. For example, a strict reading of the proposed 
restrictions on import could have prevented a traveler from reentering 
the United States from Canada or Mexico with their car if the MVAC uses 
HFC-134a. As noted in the proposed rule, the Agency's intention is to 
cover the activities of entities bringing large shipments of products 
into the country, as well as activities of entities bringing smaller 
volumes of products into the country (e.g., driving a truckload of air 
conditioning units across the Canadian or Mexican border for sale in 
the United States.). EPA therefore is distinguishing in this final rule 
those products or systems that are actively in use when travelling into 
U.S. jurisdiction from shipments of used products destined for resale 
or further distribution. EPA is not intending that this aspect of this 
rule restrict RACHP equipment in operation aboard marine vessels, 
planes, motor vehicles, refrigerated transport trailers, or intermodal 
containers. Likewise, foam or aerosol products that are in use (e.g., 
trailers) or in possession of a consumer when crossing the border are 
likewise exempt from the import prohibition. However, EPA's intent is 
to apply the use restrictions consistently for domestic manufacturers 
and importers of products. As such, no person may sell new refrigerated 
transport trailers or refrigerated intermodal containers in the United 
States, whether manufactured domestically or abroad after the 
manufacture/import compliance date, unless it complies with the HFC use 
restrictions.
    Comment: One commenter expressed concern that prohibiting the 
import of used, non-compliant products would also prevent the import of 
products intended for recycling. The commenter contended that such a 
regulated product is not `in the sector or subsector in which the 
regulated substance is used' either outside or inside the United 
States, and thus prohibiting the import is contrary to subsection 
(i)(1) of the AIM Act.
    Response: EPA considers the disposal chain, which includes the 
recycling of equipment, and not the use or reuse of the equipment in 
the relevant sector or subsector in the United States, to be outside 
the scope of the restrictions on distribution. This includes equipment 
bound for disposal that was never used by a consumer, such as defective 
components or products that were manufactured or imported illegally. 
Allowing for disposal furthers the intent of removing equipment from 
the market before it is used by the consumer.
b. Installation of Systems
    EPA is defining the term install/installation as ``to complete a 
field-

[[Page 73120]]

assembled system's circuit, including charging with a full charge, such 
that the system can function and is ready for use for its intended 
purpose.'' As discussed in section VI.A (Definitions), many commenters 
expressed concerns about EPA's proposed definition of ``manufacture,'' 
which would have included the installation and first charge of field-
assembled equipment. These included concerns that defining 
``manufacture'' to include ``install'' of field-assembled systems 
effectively accelerates the timeline of the prohibition and renders the 
one-year sell-through moot. Commenters suggested different ways to 
regulate the use of HFCs in field-assembled equipment, including 
restricting the manufacture of components that would later be field-
assembled. In this final rule, EPA is restricting the installation of 
field-assembled systems with additional clarifications. The definition 
of install is virtually identical to the proposed definition of 
manufacture for field-assembled systems. As with the term manufacture, 
the definition of ``install'' serves as a distinct point in time by 
which listed activities must be completed for purposes of meeting the 
compliance date. By proposing in its prohibitions that ``no person'' 
may manufacture a product, EPA's intent was to capture any person who 
is responsible for the manufacture (which, at proposal, included 
installation of field-assembled equipment). EPA therefore does not 
think that limiting the responsibility to only the technician who first 
charges the system (and thus makes it ready for use for its intended 
purpose) is an appropriate application of the restriction on 
installation. Doing so would be equivalent to making the final 
individual on a factory assembly line the ``manufacturer'' of a 
refrigerator and not the OEM. Responsibility for installing a system 
that improperly uses a higher-GWP HFC refrigerant after the compliance 
date lies with multiple entities, including the designer, builder, and 
owner/operator of that system, in addition to the entities that 
assembled the components and got them into operating order on site.
    Therefore, any person who assembles, contracts for, takes ownership 
of, or operates a system that is installed after the applicable 
compliance date using regulated substances prohibited for that 
subsector is in violation of this rule.
    Comment: Some commenters requested that EPA allow for installation 
of a system if building permits have already been received to avoid the 
re-design and permitting of buildings. Another commenter sought 
flexibility in case there is a delay in receiving all the necessary 
components or a delay in assembling and charging the system. The 
commenter requested EPA allow appliances purchased under contract 
before the compliance date to receive their field charge after that 
date.
    Response: EPA recognizes that some facilities may have been 
designed and permitted to specifically use systems with HFCs that will 
be restricted by this final rule. We anticipate that such instances are 
rare, especially because the final rule delays the compliance dates for 
the installation of most field-assembled systems by at least one year 
and sometimes longer depending on the subsector. However, systems using 
HFCs within facilities needing such long lead-times that they have 
approved building permits in place by the date of signature for this 
final rule are likely to be highly complex and costly to redesign. EPA 
previously granted additional time to install systems that have been 
permitted under the HCFC use restrictions under section 605(a) of the 
CAA. In those instances, EPA agreed to provide time if, among other 
conditions, those appliances were specified in a building permit dated 
before the compliance date (see 74 FR 66441, December 15, 2009) and in 
a more recent action the date of signature of the relevant proposed 
rule (see 85 FR 15267, March 17, 2020).
    Based on the comments received, similar flexibility may be needed 
in this rule. Therefore, EPA is allowing one additional year for the 
installation of systems in four subsectors if an approved building 
permit issued before the date of signature of this final rule specified 
the use of a system containing refrigerants with GWPs above the 
relevant GWP threshold for the specified subsector. These subsectors 
are: IPR systems with a January 1, 2026, compliance date; retail food 
refrigeration--supermarkets; cold storage warehouses; and ice rinks. 
This flexibility will prevent the need to redesign these systems, and 
potentially the facility that houses these systems. EPA is not 
including other subsectors in this provision as those systems are not 
typically designed specifically for an individual facility and/or those 
systems have a later compliance date and thus can make any necessary 
changes with the GWP restrictions in mind.
    EPA disagrees with the suggestion to allow systems purchased under 
contract prior to the compliance date to be field charged after that 
date. Doing so would undermine the intent of the regulation and the 
statute by incentivizing the finalization of numerous contracts in the 
days preceding the compliance date, which could then potentially allow 
for years of further installations using higher-GWP HFCs in sectors and 
subsectors that EPA has already determined under subsection (i)(4) are 
ready to transition to lower-GWP substitutes.
    Comment: Some commenters disagreed with the installation being the 
point of compliance. One commenter stated that this broadens 
responsibility for compliance from a relatively small number of 
knowledgeable OEMs to a much broader group of distribution and 
installation stakeholders who do not have the same level of awareness 
of the regulatory requirements. Another commenter recommended that EPA 
exclude ``purchaser and/or user'' and ``third party companies'' from 
the definition of a ``manufacturer,'' (under the definition as 
proposed) whether or not they are involved or provide support for 
activities associated with field assembly or charging. The commenter 
argued that the purchaser and/or user rarely, if ever, takes 
``ownership'' of IPR equipment until it is fully charged and has been 
demonstrated to run safely for the use for which it was designed and/or 
intended, which is the responsibility of the manufacturer who designed 
and fabricated the parts.
    Response: EPA disagrees with the comments that the Agency should 
only restrict OEMs and not regulate installation of a field-assembled 
system. Many commenters representing OEMs of components stated that 
they do not control how their components are used after they are sold 
to a distributor, and EPA agrees that with respect to restricting the 
use of HFCs in installation of field-assembled systems, OEMs of 
components used in those systems are not the appropriate entity to 
regulate (unless the OEM is involved in the design or construction of 
the system). While applying the restrictions on installations to the 
parties other than OEMs results in more potentially regulated entities, 
it appropriately places the restriction on the entities that can 
control the use of HFCs in that system. While a broader group of 
installation stakeholders may not be as accustomed to compliance issues 
as the relatively smaller group of component OEMs that commenters 
requested be subject to the restrictions, applying the restrictions for 
installation of systems to the designer, builder, and owner/operator of 
that system will help to ensure that there is a knowledgeable party 
driving compliance.
    Comment: Many commenters requested that EPA provide a precise and 
clear definition for when a field-erected and field-charged system 
modified as part of a remodel or regular

[[Page 73121]]

maintenance is covered by the new GWP limit. They requested that EPA 
allow for replacement of appliance components, including but not 
limited to cases, compressors, valves, condensers, evaporator units, 
piping and other components to keep that existing system running. They 
also requested that EPA allow for remodels or retrofits to update the 
look, improve the efficiency, or reduce leaks in a system. Other 
commenters requested that EPA use California's definitions of new 
refrigeration equipment, new air-conditioning equipment, and new 
facility to demarcate which modifications to a system trigger the 
requirements applicable to new systems. A State commenter noted that a 
single, unified definition of `new' would be useful for States that 
wish to establish controls that are aligned with EPA and in cases where 
stakeholders require clarity on State versus national controls.
    Several commenters summarized California's regulations as an 
example of how a previously installed refrigeration system could 
trigger the use restriction through either of two methods. The first 
method is when the compressor capacity of the refrigeration system is 
increased or the cost of replacing components over a three-year period 
exceeds 50 percent of the capital cost of replacing the entire system 
(excluding display cases).\44\ The second method is when an existing 
facility changes to a different end-use or when 75 percent of the 
refrigeration system's evaporators (by number) and 100 percent of its 
compressor racks, condensers, and connected evaporator loads have been 
replaced. A previously installed air-conditioning system triggers the 
use restriction depending on the size of the system. For systems with a 
single condenser and single evaporator, the use restrictions are 
triggered when replacing the exterior condenser, condensing unit, or 
remote condensing unit. For systems having more than one condenser and/
or more than one evaporator, the use restrictions are triggered when 75 
percent of the indoor evaporator units (by number) and 100 percent of 
the air source or water source condensing units are replaced over a 
three-year period.
---------------------------------------------------------------------------

    \44\ This is similar to the definition of ``new'' in New York 
State. Specifically, new is defined as ``Products or equipment that 
are manufactured after the effective date of this Part or installed 
with new or used components, expanded by the addition of components 
to increase system capacity after the effective date of this Part, 
or replaced or cumulatively replaced after the effective date of 
this Part such that the cumulative capital cost of replacement 
exceeds 50% of the capital cost of replacing the whole system.'' 6 
NYCRR 494.3(s).
---------------------------------------------------------------------------

    A commenter recommended EPA use the first method to avoid the 
continuous replacement of parts indefinitely without ever triggering 
any restriction on the use of controlled substances. An industry 
commenter recommended the second method. A few commenters also 
requested that EPA define the term ``new facility'' which is 
substantively the same as the second method in the definition for new 
refrigeration equipment. One such commenter that favored this approach 
said it is clearer that components may be replaced and that restricting 
``new refrigeration equipment'' would require establishing exceptions 
for remodels and replacement for maintenance.
    Response: EPA's intention is to allow the ordinary servicing and 
repair of equipment and not to apply restrictions in a way that would 
prevent such maintenance. However, we are cognizant of the concern that 
systems could be significantly modified or upgraded to the point that 
such modification or upgrade should be considered a new installation 
subject to the subsector GWP limits.
    The Agency has encountered the question of what modifications 
constitute the installation of a new system during the phaseout of 
HCFCs. Under section 605(a) of the CAA, EPA prohibited the use of 
virgin HCFC-22 and HCFC-142b to charge new appliances assembled onsite 
on or after January 1, 2010. (December 15, 2009; 74 FR 66437). In that 
context, the Agency's interpretation was that there were two different 
situations that could be equivalent to the manufacture (i.e., 
installation) of a new system. These are modifications to a system that 
increase the total cooling capacity in BTU of the system or the 
complete replacement of all components within a system at once or over 
time. Based on commenters' requests for clarification on the issue, EPA 
is adopting these two situations in the regulatory text. In addition, 
after consideration of the public comments and its past experience 
implementing similar restrictions, the Agency is providing more 
specificity about which components must be replaced in order for a 
replacement to qualify as ``new installation.''
    EPA noted in the proposed rule, in the context of what qualifies as 
``equipment in existence,'' that ``in limited cases where every part of 
a piece of equipment had been altered or replaced,'' such equipment 
would fall outside the statutory and regulatory exemption in subsection 
(i)(7)(B), and the alteration or replacement would be considered a new 
installation subject to the restrictions under this section. In so 
doing, we did not intend that ``every'' piece would include refrigerant 
tubing, which is often very difficult to replace because the tubing may 
be inaccessible. Even in major overhauls of systems, this tubing is 
rarely replaced, and we therefore think replacements where this tubing 
remains installed should still be considered new installations for 
purposes of triggering these restrictions. Therefore, we are clarifying 
in this final rulemaking and in the regulatory text which components 
must be replaced, and at what percentages, to provide a precise, clear 
standard that will ensure that major replacements and alterations are 
properly subject to the restrictions and transition to lower-GWP 
refrigerants. Specifically, when 75 percent of the refrigeration 
system's evaporators (by number) and 100 percent of its compressor 
racks, condensers, and connected evaporator loads have been replaced, 
such replacement constitutes a new installation and is subject to the 
restrictions on installation. EPA's approach in this final rulemaking 
is also used by States that have adopted a definition of ``new 
refrigeration equipment.''
    EPA disagrees with commenters' suggestion that the Agency adopt 
other methods used in California for determining when an existing 
refrigeration system is considered ``new.'' Those other methods, such 
as including specific timeframes or assessing capital costs, deviate 
from EPA's historical interpretations under title VI of the CAA and 
raise additional questions about implementation. Nor is EPA adopting 
the method for determining when an existing air-conditioning system 
with a single condenser and single evaporator is considered ``new.'' In 
implementing the use restriction on HCFC-22 under title VI of the CAA, 
EPA has considered the replacement of the condensing unit to be a 
repair and not the installation of a new system. EPA finds that it is 
also reasonable to continue that interpretation under the use 
restrictions in subsection (i) as it is the same type of equipment and 
because the AIM Act is implementing a phasedown rather than a phaseout, 
meaning there is no end date for the production and import of bulk 
HFCs.
c. Sale or Distribution of Factory-Completed Products
    As discussed above, EPA interprets ``use'' to include activities in 
the market chain that occur after the manufacture or import of a 
product. As such, EPA is applying use restrictions to any person who 
sells, distributes, offers for sale or

[[Page 73122]]

distribution, makes available for sale or distribution, purchases or 
receives for sale or distribution, or attempts to purchase or receive 
for sale or distribution, or exports any product using a regulated 
substance in the sectors or subsectors controlled under subsection (i). 
Applying the restrictions in this way ensures that the goal of 
restricting the use of regulated substances in the sectors or 
subsectors in which the regulated substances are used can be achieved, 
because the sector and subsector's use of the regulated substance is 
present in all these aspects of the market chain, and it is EPA's 
intention to restrict use across that chain. Therefore, if a 
manufacturer or importer improperly introduces into the U.S. market a 
non-compliant product, distributors and retailers (including online 
retailers) offering that product for sale are also restricted from 
covered activities related to that product. Providing the means by 
which individuals are able to list and sell prohibited products, or 
exerting control over these sales, including operating platforms for 
eCommerce transactions, will be considered use under this rule. EPA is 
also applying the use restrictions to those entities who purchase or 
receive for the purpose of further sale or distribution with the intent 
to cover both sides of the transaction between distributors but not the 
purchase by a consumer. The intent of this restriction is to ensure 
that products that do not meet the limits do not enter the market and 
are not circulated in the market, prior to sale to the consumer.
    EPA proposed to prohibit sale, distribution, offer for sale and 
distribution, and export of products using regulated substances not 
meeting the GWP limits one year after the proposed prohibition date for 
manufacture and import of products using regulated substances over the 
GWP limits in each subsector. EPA explained at proposal that limiting 
the period of time when products that do not meet the GWP limits can 
continue to be sold has advantages over indefinitely exempting the sale 
of inventory that does not meet the established use restrictions. In 
particular, we noted the advantage of having a date certain by which 
all parties--e.g., the public, enforcement officials, and regulated 
entities--know that there can legally be no new products on the market 
that do not meet the GWP limits. This additional prohibition on the 
activities subsequent to manufacture and import but prior to sale to 
the consumer reinforces the sector or subsector's transition away from 
use of HFCs in new products and, to the extent that it is a 
possibility, prevents the stockpiling and continued sale of products 
that do not meet the sector or subsector use restrictions from 
continuing indefinitely into the future.
    EPA received many comments on this proposed prohibition on the sale 
or distribution of products. Comments received on this aspect of this 
rule and EPA's responses to those comments are summarized and discussed 
in further detail below and in the response to comments document, 
available in the docket.
    This final action retains a limited sell-through period on products 
using a regulated substance that do not meet the sector and subsector 
restrictions with key changes in response to concerns raised by the 
commenters. First, EPA is limiting the prohibition on sale, 
distribution, offer for sale and distribution, and export to factory-
completed products that use prohibited higher-GWP regulated substances. 
As discussed in greater detail later in this section, EPA is excluding 
components and allowing for their continued manufacture, import, sale, 
distribution, offer for sale and distribution, and export, subject to 
certain restrictions, including that these uses are for the purpose of 
servicing existing equipment. Second, EPA is extending the compliance 
date for the sales prohibition on factory-completed products from the 
proposed one year to three years after the manufacture and import 
compliance date. EPA provided the two additional years to address 
commenters' concerns that a one year sell-through was potentially 
insufficient to clear inventory, and in particular, seasonal products 
such as window-unit air conditioners, which can experience variable 
demand from year-to-year. This final approach ensures that sectors and 
subsectors that use regulated substances will transition from the use 
of those substances where such transition is appropriate and alleviates 
the concerns raised by commenters.
    Comment: Several commenters voiced concern that the one-year 
compliance deadline would create the risk of stranded inventory that 
would not be able to be sold, which would cause economic harm to 
manufacturers, distributors, retailers, and ultimately consumers. 
Commenters representing distributors highlighted the many 
considerations they must account for in determining the amount of 
inventory to stock, citing the desire to carry amounts of inventory 
large enough to maintain competitive pricing, against costs incurred 
via storage space leasing, warehouse mortgages, building utilities, and 
insurance on products stored in the warehouse. Other commenters, 
particularly those in the heating and cooling sector, noted that many 
factors, including the economy, weather, and demand for construction 
impact sales and that in this sector particularly, it is already 
difficult to forecast what amount of inventory will need to be carried 
over year to year. Many commenters noted that the sell-through 
limitation would exacerbate existing supply chain challenges, 
particularly for small businesses. Commenters stated that the one-year 
sell-through period would require distributors to either stock less 
inventory, and therefore potentially fail to meet customer demand, or 
to throw away inventory that would be prohibited by the sell-through 
limitation, and that either of these outcomes would cause economic 
harm. Commenters noted that the economic harm caused by the proposed 
one-year sell-through period might cause them to reduce their labor 
forces, and would require increased monitoring for compliance 
throughout the supply chain.
    Many of these commenters also cited concerns about potential 
adverse environmental impacts of stranding inventory. Others noted that 
the environmental benefit of the AIM Act is from the phasedown of the 
supply of HFCs, and that the HFC price increases and lack of 
availability of regulated substances that will flow from the phase-down 
will provide a market force to transition to lower-GWP substitutes, 
making the sell-through limitation unnecessary as a backstop. Many 
commenters requested that EPA eliminate the sell-through limitation 
altogether, and instead permit unlimited sell-through of any product 
labeled with a ``date of manufacture'' meeting the compliance date for 
manufacture. Others requested that the Agency at least extend the 
permissible limitation to multiple years, with some commenters 
suggesting that two or three years would minimize the risk of stranded 
inventory.
    EPA also received comments in support of its proposed prohibition 
on sale, distribution, offer for sale and distribution, and export. 
Some commenters stated that the compliance dates in the proposed rule 
already provide sufficient time for manufacturers and distributors to 
plan for the transition to lower-GWP substitutes and to sell existing 
inventories, and that the compliance date for the sell-through 
limitation should be one year at most. These commenters asserted that 
allowing an indefinite period for sell-through of

[[Page 73123]]

equipment manufactured by the manufacture compliance date would 
complicate enforcement and could provide an incentive for companies to 
increase near term production of systems using HFCs before restrictions 
come into effect. The Agency also received supportive comments on the 
proposed sell-through limitation from States, including one that has 
promulgated under State law a prohibition on manufacture but allows 
unlimited sell-through of products manufactured prior to that 
prohibition date. That State commenter noted that the unlimited sell-
through approach can create challenges because it relies on regulated 
entities to provide documentation as to the manufacture date, and that 
not all entities in the market chain can provide that information.
    Response: EPA acknowledges the input provided by commenters both in 
support of and raising concerns with the limitation on sale, 
distribution, and export of products regulated under these 
restrictions. We recognize that the production and purchase of products 
or components that are unable to be sold to consumers is an economic 
and environmental outcome no parties desire, and the proposed rule's 
forward-looking compliance dates were intended to allow all parties in 
the market supply chain sufficient time to avoid that outcome. To that 
end, after considering the concerns raised by various commenters, EPA 
is extending the proposed one-year compliance date for the sell-through 
limitation on products to three years after the manufacture and import 
compliance date. The longer timeframe for a sell-through allows 
regulated entities more time to manage inventory to avoid purchasing 
products they will not be able to

[…truncated; see source link]
Indexed from Federal Register on October 24, 2023.

This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.