Waste Management System; Testing and Monitoring Activities; Final Rule: Methods Innovation Rule and SW-846 Final Update IIIB, 34538-34592 [05-10197]
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Federal Register / Vol. 70, No. 113 / Tuesday, June 14, 2005 / Rules and Regulations
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Parts 63, 258, 260, 261, 264,
265, 266, 268, 270, 271, and 279
[RCRA–2002–0025; FRL–7916–1]
RIN 2050–AE41
Waste Management System; Testing
and Monitoring Activities; Final Rule:
Methods Innovation Rule and SW–846
Final Update IIIB
Environmental Protection
Agency (EPA).
ACTION: Final rule.
AGENCY:
SUMMARY: The Environmental Protection
Agency is amending a variety of testing
and monitoring requirements in the
Resource Conservation and Recovery
Act (RCRA) hazardous and nonhazardous solid waste regulations and
for certain Clean Air Act (CAA)
regulations that relate to hazardous
waste combustors. These amendments
allow more flexibility when conducting
RCRA-related sampling and analysis by
removing from the regulations a
requirement to use the methods found
in ‘‘Test Methods for Evaluating Solid
Waste, Physical/Chemical Methods,’’
also known as ‘‘SW–846,’’ in conducting
various testing and monitoring and by
limiting required uses of an SW–846
method to circumstances where the
method is the only one capable of
measuring the particular property (i.e.,
the method is used to measure a
required method-defined parameter).
This action is an important step forward
in implementing the use of a
performance-based approach, which is
part of the Agency’s efforts toward
Innovating for Better Environmental
Results. Additionally, the Agency is
making certain other clarifications and
technical amendments. These changes
should make it easier and more cost
effective to comply with the affected
regulations, without compromising
human health or environmental
protection.
DATES: This final rule is effective on July
14, 2005. The incorporation by reference
of certain publications listed in the rule
is approved by the Director of the
Federal Register as of July 14, 2005.
ADDRESSES: EPA has established a
docket for this action under Docket ID
No. RCRA–2002–0025. All documents
in the docket are listed in the EDOCKET
index at https://www.epa.gov/edocket.
Although listed in the index, some
information is not publicly available,
i.e., CBI or other information for which
disclosure is restricted by statute.
Certain other material, such as
copyrighted material, is not placed on
the Internet and will be publicly
available only in hard copy form.
Publicly available docket materials are
available either electronically in
EDOCKET or in hard copy at the
OSWER RCRA Docket, EPA/DC, EPA
West, Room B102, 1301 Constitution
Ave., NW., Washington, DC. The Public
Reading Room is open from 8:30 a.m. to
4:30 p.m., Monday through Friday,
excluding legal holidays. The telephone
number for the Public Reading Room is
(202) 566–1744. This Docket Facility is
open from 8:30 a.m. to 4:30 p.m.,
Monday through Friday, excluding legal
holidays. The Docket telephone number
is (202) 566–0270.
FOR FURTHER INFORMATION CONTACT: For
information on this rulemaking, contact
Kim Kirkland at: Office of Solid Waste
(5307W), U. S. Environmental
Protection Agency, 1200 Pennsylvania
Avenue, SW., Washington, DC 20460–
0002, (703) 308–8855, e-mail address:
kirkland.kim@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does This Action Apply to Me?
You may be covered by this action if
you conduct waste sampling and
analysis for Resource Conservation and
Recovery Act (RCRA)-or National
Emission Standards for Hazardous Air
Pollutants (NESHAP)-related activities.
Covered entities include anyone who
generates, treats, stores, or disposes of
hazardous or nonhazardous solid waste
and is subject to RCRA subtitle C or D
sampling and analysis requirements;
and entities subject to NESHAP final
standards for hazardous waste
combustors (40 CFR part 63, subpart
EEE). All types of industries,
governments, and organizations may
have entities that generate or manage
RCRA-regulated hazardous and
nonhazardous solid wastes and may be
subject to RCRA-related sampling and
analysis requirements.
To determine whether your facility,
company, business organization, etc., is
covered by this action, you should
carefully examine the applicability
criteria in part 63 and in parts 258
through 299 of the Code of Federal
Regulations. If you have questions
regarding the applicability of this action
to a particular entity, consult your
regulatory authority.
B. How Do I Obtain Copies of SW–846?
The Third Edition of SW–846, as
amended by Final Updates I, II, IIA, IIB,
III, IIIA, and IIIB will be available in pdf
format on the Internet at https://
www.epa.gov/SW–846. A paper copy of
Final Update IIIB is also located in the
docket for this rule (see section I.A
above). Table 1 below provides sources
for both paper and electronic copies of
the Third Edition of SW–846 and all of
its updates.
TABLE 1.—SOURCES FOR SW–846, THIRD EDITION, AND ITS UPDATES
Source
Available portions of SW–846
Superintendent of Documents, U.S. Government Printing Office (GPO), Washington, DC 20402, phone (202) 512–
1800, toll free (866) 512–1800, fax orders (202) 512–2250,
and online: https://bookstore.gpo.gov.
National Technical Information Service (NTIS), 5285 Port
Royal Road, Springfield, VA 22161, (703) 605–6000 or
(800) 553–6847.
—Paper copies of the SW–846, Third Edition, basic manual and of certain updates, including Final Updates, I, II, IIA, IIB, III, and IIIB and Draft Update IVA.
The subscriber must integrate the updates.
Internet: https://www.epa.gov/SW-846 .......................................
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—Paper copy of an integrated version of SW–846, Third Edition, as amended by
Final Updates, I, II, IIA, IIB, III, and IIIA.
—Individual paper copies of the SW–846, Third Edition, basic manual and of certain updates, including Final Updates I, II, IIA, IIB, III, IIIA, and IIIB and Draft
Updates IVA and IVB.
—CD-ROM of integrated version of SW-846, Third Edition, as amended by Final
Updates I, II, IIA, IIB, and III (pdf and WordPerfect electronic copies).
—CD-ROM of Draft Update IVA (pdf and WordPerfect electronic copies).
—Integrated version of SW-846, Third Edition, as amended by Final Updates I,
II, IIA, IIB, III, IIIA, and IIB (pdf electronic copy).
—Draft Update IVA (pdf electronic copy).
—Draft Update IVB (pdf electronic copy).
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Federal Register / Vol. 70, No. 113 / Tuesday, June 14, 2005 / Rules and Regulations
C. Regulatory Flexibility Act
D. Unfunded Mandates Reform Act
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
J. Executive Order 12898: Federal Actions
to Address Environmental Justice in
Minority Populations and Low-Income
Populations
K. Congressional Review Act
C. What Is the Legal Authority for This
Action?
We are promulgating the part 258,
260, 261, 264–266, 268, 270, 271, and
279 regulations under the authority of
sections 1006, 2002(a), 3001–3007,
3010, 3013–3018, and 7004 of the Solid
Waste Disposal Act, as amended by the
Resource Conservation and Recovery
Act of 1976, as amended. We are
promulgating the part 63 regulation
under the authority of sections 112 and
114 of the Clean Air Act.
D. How Is the Rest of This Preamble
Organized?
II. Summary of Today’s Rule
III. Background and Purpose of Action To
Reform RCRA-Related Testing and
Monitoring
A. Public Comments Regarding How to
Determine if a Method Is Appropriate
B. Public Comments Regarding Other
Approaches
C. Public Comments Regarding Impacts
From Removal of Required Uses of SW–
846 Methods
IV. Regulatory Revisions Involving Removal
of SW–846 Requirements
V. Editorial Corrections to SW–846
References in the RCRA Testing and
Monitoring Regulations
VI. Action to Withdraw the Reactivity
Interim Guidance from SW–846 Chapter
Seven and Remove Required SW–846
Reactivity Analyses and Threshold
Levels from Conditional Delistings
VII. Clarifications to Corrosivity and
Ignitability Hazardous Waste
Characteristics
A. Revision to § 261.22(a)(2) to Clarify that
SW–846 Method 1110A Is the SW–846
Standardized Version of the NACE
Standard Specified for Corrosivity
Characteristic Testing
B. Revisions to § 261.21(a)(1) to Remove an
Unnecessary Referral to Method
Equivalency Petitions; and an
Explanation regarding the Decision to
Not Revise the Regulation to Include the
Updated ASTM Standards and
References to Methods 1010A and 1020B
as Proposed
VIII. Availability of Final Update IIIB and
Status of Final Update IV to SW–846
IX. Addition of Method 25A to
§§ 264.1034(c)(1)(ii) and (iv) and
265.1034(c)(1)(ii) and (iv)
X. Removal of Requirements from
§ 63.1208(b)(8)(i) and (ii) in the NESHAP
Standards to Demonstrate Feedstream
Analytes Are Not Present at Certain
Levels
XI. Status of the RCRA Waste Sampling Draft
Technical Guidance
XII. State Authorization Procedures
A. Applicability of Federal Rules in
Authorized States
B. Authorization of States for Today’s Rule
C. Abbreviated Authorization Procedures
XIII. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory
Planning and Review
B. Paperwork Reduction Act
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II. Summary of Today’s Rule
On October 30, 2002 (67 FR 66251–
66301), the Environmental Protection
Agency (EPA) proposed to amend the
testing and monitoring requirements
under the hazardous and nonhazardous
solid waste regulations, and a testing
requirement under the Clean Air Act
(CAA) in the National Emission
Standards for Hazardous Air Pollutants
(NESHAP) for hazardous waste
combustors. EPA is finalizing those
regulatory revisions at this time. Some
of the public comments are summarized
and addressed in the sections to follow,
and a background document containing
our responses to all public comments
can be found in the docket to this rule,
RCRA–2002–0025. After consideration
of all comments and for the reasons
summarized in today’s rule, we are
finalizing the following actions:
1. Reforming RCRA-related testing
and monitoring by restricting
requirements to use SW–846 to only
those situations where the method is the
only one capable of measuring the
property (i.e., it is used to measure a
method-defined parameter). This will
allow more flexibility in RCRA-related
sampling and analysis by removing
unnecessary required uses of SW–846.
2. Withdrawing the cyanide and
sulfide reactivity guidance from sections
7.3.3 and 7.3.4 of SW–846 Chapter
Seven and withdrawing required uses of
reactive cyanide and sulfide methods
and threshold levels from conditional
delistings.
3. Amending the regulations for the
ignitability and corrosivity hazardous
waste characteristics. As part of this, we
are clarifying in § 261.22(a)(2) that SW–
846 Method 1110A, ‘‘Corrosivity
Toward Steel,’’ is the ‘‘standardized’’ (as
described in § 261.22(a)(2)) SW–846
method that is required to be used to
determine the characteristic of
corrosivity for steel. We are also
removing the unnecessary reference to
equivalency petitions in the ignitability
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characteristic at § 261.21(a)(1). However,
regarding the methods required for the
determination of flash point under the
characteristic of ignitability, the Agency
decided not to replace the standard test
methods ASTM D 3278–78 and D 93–79
with the latest versions of those
methods.
4. Incorporating by reference Update
IIIB to SW–846, which includes the
revised Chapter Seven, and eleven
revised methods, including method
revisions to remove a requirement to use
the SW–846 Chapter Nine, ‘‘Sampling
Plan.’’
5. Adding Method 25A as an
analytical option to analyses conducted
in support of air emission standards for
process vents and/or equipment leaks at
treatment, storage, and disposal
facilities.
6. Removing a requirement to
demonstrate that feedstream analytes
are not present at levels above the 80%
upper confidence limit above the mean
for sources subject to NESHAP: Final
Standards for Hazardous Waste
Combustors.
7. Removing from the regulations
unnecessary references to SW–846,
which do not affect the intent of the
RCRA regulation.
This rule does not add any additional
requirements to the regulations. Instead,
this rule removes the requirement to use
SW–846, and it clarifies what the
Agency believes should be considered
during the selection of other appropriate
methods. Our purpose for the regulatory
revisions is to make it easier and more
cost effective to comply with the RCRA
regulations by allowing more flexibility
in method selection and use. If you
prefer, where you find that a specific
SW–846 method yields data that is
suitably effective for demonstrating
compliance in the particular matrix
being analyzed, you can still use the
SW–846 methods.
III. Background and Purpose of Action
to Reform RCRA-Related Testing and
Monitoring
Typically, the hazardous and
nonhazardous solid waste RCRA
regulations for testing and monitoring
activities or the permits or waste
analysis plans of facilities regulated by
RCRA specify the analytes of concern to
be determined in a matrix of concern at
a particular regulatory level of concern.
Additionally, some recently
promulgated regulations specify the
confidence level of concern. Most of the
RCRA regulations leave the how (i.e.,
which test method to use) up to the
regulated community. Some RCRA
regulations, however, specify the use of
methods from the EPA publication
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Federal Register / Vol. 70, No. 113 / Tuesday, June 14, 2005 / Rules and Regulations
‘‘Test Methods for Evaluating Solid
Waste, Physical/Chemical Methods,’’
also known as ‘‘SW–846.’’
Initially, EPA issued SW–846 in 1980
soon after the first RCRA regulations
were published. At that time, we
intended that SW–846 serve two roles.
First, the Agency intended that it serve
as a guidance manual of generally
appropriate and reliable analytical
methods for RCRA-related testing and
monitoring. Second, we intended that it
serve as a readily-available source of
those few analytical methods which
were required in order to comply with
the RCRA regulations. Since that time,
EPA published regulations that required
the use of SW–846 methods in general.
Subsequently, members of the regulated
public made it clear to EPA that they
would like the opportunity to use other
reliable methods, and EPA also decided
that some of the SW–846 requirements
were not necessary.
The regulatory requirement to use
SW–846 in general (e.g., as in the
delisting regulations at § 260.22 prior to
this final rule) did not identify specific
SW–846 methods. Rather, this
requirement typically included the
regulation of many different analytes
which could be determined by many
different methods. Almost every update
to SW–846 includes at least one method
that may be applicable to one or more
of these general analytical requirements.
Therefore, whenever SW–846 was
updated to revise or add methods, EPA
had to incorporate by reference all of the
new and revised methods into the RCRA
regulations as part of a rulemaking. EPA
issued the updates as a proposed rule,
requested public comment, and then
promulgated the update in a final rule.
This lengthy process delayed the timely
use of the new analytical technologies.
On October 30, 2002 (67 FR 66251–
66301), EPA proposed to remove from
the regulations a requirement to use a
method found in SW–846, except when
that method is the only one capable of
measuring the particular property. At
that time, we described our reasons for
wanting to remove this requirement
from the regulations, including the
Agency’s desire to fully implement a
performance-based measurement system
(PBMS) in the RCRA program.
Specifically, we noted that such a
change would: (1) Allow the regulated
community more flexibility in method
use during RCRA-required testing; (2)
stimulate the development and timely
use of innovative and more costeffective monitoring technologies and
approaches in the RCRA program; (3)
allow more efficient and timely releases
of SW–846 methods by decoupling most
of the methods from required uses in the
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RCRA regulations; and (4) make the
RCRA program more effective by
focusing on measurement objectives
rather than on measurement
technologies. As noted, the Agency
proposed to restrict the requirement to
use a specific SW–846 method to only
those situations where its particular
procedure is the only one that is capable
of measuring the property (i.e., a
method-defined parameter, or MDP).
For example, to determine whether the
levels of hazardous constituents in a
particular waste stream are equal to or
greater than the toxicity characteristic
(TC) levels specified in § 261.24, waste
generators must test their waste using
SW–846 Method 1311, the ‘‘Toxicity
Characteristic Leaching Procedure,’’ or
‘‘TCLP.’’ If levels in the waste are
greater than or equal to the TC levels,
the waste is a hazardous waste and is
subject to the RCRA hazardous waste
regulations. This is the only reliable
method for determining whether TC
levels are met. Thus, testing of any
material to determine whether it meets
the Toxicity Characteristic levels must
be done using the TCLP. EPA describes
the measurement obtained from the
TCLP, as well as from certain other
methods, as a required ‘‘method-defined
parameter.’’
We requested public comment on the
proposed revisions to the RCRA
regulations, although not to the methoddefined parameters, and received
comments on the proposed action from
over 20 different commenters, which
included representatives of Federal
Government agencies, State Government
agencies, industry, waste generation and
management entities, and analytical
laboratories. The majority (86%) of the
commenters generally supported, with
comment, the MIR action and EPA’s
efforts to allow more flexibility in
method selection when conducting
RCRA-related sampling and analysis.
Regarding the positive comments, one
commenter, a state agency
representative, applauded EPA for
recognizing that regulating does not
have to be prescriptive. Another
commenter, a representative of
analytical laboratories, believed that the
additional flexibility will result in data
quality improvements. Two
representatives of waste generation or
management entities concurred with
EPA that the majority of the MIR
revisions should make it easier and
more cost effective to comply with
RCRA-related regulations.
For the most part, the negative public
comments may have reflected a
misunderstanding of certain important
aspects and premises of the MIR, which
we are clarifying in our responses to
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those comments. With respect to other
negative comments, the Agency expects
that the discussion below will further
clarify the purposes and premises of the
MIR, and will clarify options for dealing
with the inherent flexibility of this
approach. Also, the Agency will
continue to provide training on the
concepts of this rule to further clarify its
intent and support its implementation.
You will find a background document
containing our complete responses to all
relevant public comments in the docket
to this rule, docket number RCRA–
2002–0025, at the location listed above
under ADDRESSES. Some of the public
comments are also addressed within
this preamble to the final rule.
Based on our review of the public
comments regarding the October 30,
2002 proposed rule, we are proceeding
with publication of this final rule,
which finalizes the proposed revisions
to the RCRA regulations. That is, this
rule removes unnecessary required uses
of SW–846 in general and it removes
any unnecessary required uses of
specific SW–846 methods. Other
reliable methods can now be used by
the regulated public for compliance
with the affected regulations. This
action also encourages the timely use of
new and innovative methods outside of
SW–846 in that, for most sampling and
analysis scenarios, it will not be
necessary to submit an equivalency
petition when using a non-SW–846
method. However, some regulations will
still require use of a specific SW–846
method when that method is for
determination of a RCRA-required
method-defined parameter (MDP); in
those cases, a regulated entity has to
submit an equivalency petition and
receive approval of that petition from
the Agency before an alternative method
can be used.
This final rule will allow the Agency
to make final updates to SW–846
available in a more timely manner. For
example, soon after publication of this
document, we will announce the
availability of Final Update IV (see
section VIII of this document). The
methods of Final Update IV did not
have to go through the rulemaking
process because, with publication of
this final rule, SW–846 is no longer
required in general by any existing
RCRA regulation and none of the new
or revised methods in Update IV are
specifically required by any RCRA
regulation for the analysis of methoddefined parameters (MDPs). However,
we did solicit and consider public
comments on the methods through
Federal Register notices, see 63 FR
25430–25438, May 8, 1998 (Draft
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Update IVA), and 65 FR 70678–70681,
November 27, 2000 (Draft Update IVB).
A. Public Comments Regarding How To
Determine if a Method Is Appropriate
In section III.A of the preamble to the
October 30, 2002 proposed rule, we
discussed our proposed revisions to
remove the requirement to use SW–846
methods by adding regulatory language
allowing the use of appropriate methods
such as those found in SW–846 or other
reliable sources. In the preamble of the
proposed rule, we provided guidance on
how to determine if a method is
appropriate for its analytical purpose.
Specifically, we mentioned that such a
method might be one published by EPA
in a different manual or regulation or
published by another government
agency, a voluntary standards setting
organization, or other well-known
sources. We also proposed to retain
mention of the SW–846 methods in the
regulations as guidance and as examples
of methods that could be appropriate.
In the proposed rule preamble, we
gave two primary considerations in
selecting an appropriate method, which
together serve as our general definition
of an appropriate method. As done in
the preamble to the proposed rule, the
text to follow explains each of these
concepts and identifies other guidance
that may be helpful to the regulated
community.
1. Appropriate methods are reliable
and accepted as such in the scientific
community.
2. Appropriate methods generate
effective data.
Regarding the first consideration, we
noted that methods which are reliable
and accepted in the scientific
community might include those
published by the Agency or other
government entities using techniques
that have documented reliability. SW–
846 methods, for example, are reviewed
by a technical workgroup composed of
national expert-level chemists who
provide peer input and determine
whether method reliability is
sufficiently documented. The technical
reliability and acceptance of other
methods published by other
governmental or non-governmental
organizations may also be documented,
especially if the methods are subjected
to some form of objective scientific
review. For instance, to qualify for
recognition as having developed a
voluntary consensus standard (e.g.,
analytical method) under the National
Technology Transfer & Advancement
Act of 1995 (NTTAA), an organization
must produce standards by consensus,
observe the principles of openness and
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balance of interests, and provide due
process, including an appeals process.
Regarding the second consideration in
the identification of appropriate
methods—generation of effective data—
we described in the preamble to the
proposed rule examples of tools that
might be used in this determination.
This consideration is project-specific
and therefore the tools and criteria will
be different for each analytical effort. As
stated in the proposed rule preamble,
effective data are data of sufficiently
known and appropriate quality to be
used in making project-specific
decisions. An example of such a
decision is whether a particular waste is
hazardous because a constituent of
concern is present above a level of
concern. Before sampling and analysis
begins, project planners should identify
why the analysis is being done, how the
data will be used, and how ‘‘good’’ the
data has to be (e.g., the quality
objectives for the project as established
through a systematic planning process).
Effective data meet the quality
objectives set by the project planners for
the specific project. The quality
objectives should be rationally and
systematically identified during the
planning of the project and
development of the project-specific
Quality Assurance Project Plan (QAPP),
Waste Analysis Plan (WAP), Sampling
and Analysis Plan (SAP), or other
appropriate systematic planning
document. Sampling and analysis
documentation should be sufficient to
confirm that the data are effective and
that the selected method is appropriate.
Quality objectives generally refer to
the necessary quality of the overall
decision to be made or, in other words,
the tolerable error (i.e., acceptable level
of uncertainty for the decision). For
example, a quality objective for waste
analysis may be that one must
demonstrate that an analyte is not
present above the reported level at the
80 percent upper confidence around the
mean, and that the method could have
detected the presence of the analyte at
that level and confidence limit. A
quality objective may be specified in a
regulation, a permit, a corrective action
agreement, or other regulatory or
enforcement document. Sometimes you
must consider a quality objective
regulatory specification when selecting
an appropriate method. For example,
the RCRA comparable fuels’ provisions
include quality objectives in lieu of
naming the use of specific methods (see
63 FR 33781, June 19, 1998). You can
find guidance on the development of
formal data quality objectives (DQOs) in
EPA’s ‘‘Guidance for the Data Quality
Objectives Process’’ (EPA QA/G–4)
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found at EPA’s Quality Staff’s Web site
(https://www.epa.gov/quality/), in
Chapter One, ‘‘Quality Control,’’ of SW–
846, and in ASTM D 5792, ‘‘Standard
Practice for Generation of
Environmental Data Related to Waste
Management Activities: Development of
Data Quality Objectives.’’ You may also
use other scientifically valid systematic
planning processes for developing
quality objectives based on specific
project needs.
In the project planning document, you
should identify the types of quality
control (QC) concepts (e.g., spike
recovery analyses, blanks, etc.) you will
use to determine if you meet your
objectives. For example, selection of an
appropriate method is sometimes
demonstrated by adequate recovery of
spiked or surrogate analytes and
reproducible results, or through
successful analysis of a standard
reference material of a matrix-type
analogous to that of the actual sample
matrix. The method may not be
appropriate for its intended use if your
data show inadequate recovery of an
analyte at a level that impairs a decision
regarding whether the analyte is present
at or below its regulatory level. Such a
method would not generate effective
data. Based on your QC data, you
should determine whether the method
generates results that are sufficiently
sensitive, unbiased, and precise to
demonstrate compliance with the
subject regulation.
However, you should not just focus
on controlling or documenting
analytical quality, because regulatory
decisions are also susceptible to error
due to sampling procedures. If the
contaminant variability is not properly
addressed during the planning and
collection of samples, an incorrect
decision could be reached even though
the method performed well in terms of
laboratory quality control. No matter
how accurate or precise the laboratory
analysis, the data will provide
misleading information if excessive
error is introduced by improper
sampling procedures. Guidance on
identifying the necessary quality control
procedures and on minimizing the
potential for both analytical and
sampling error can be found at the EPA
Quality Staff’s Web site (https://
www.epa.gov/quality/) or in Chapters
One, Two, and Nine of SW–846. In
addition, guidance on determining and
demonstrating the appropriateness of a
selected measurement method for a
particular application may be found in
ASTM D 6956–03, ‘‘Standard Guide for
Demonstrating and Assessing Whether a
Chemical Analytical Measurement
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System Provides Analytical Results
Consistent with Their Intended Use.’’
Finally, EPA noted in the proposed
rule preamble that you should identify
appropriate methods for a specific
project before sampling and analysis
begins. As the regulated entity, you are
ultimately responsible for compliance
with a particular regulation. Therefore,
you should not rely on the laboratory or
other project participant to select an
appropriate method. We recommend
that you consult with your regulating
authority during identification of
performance goals and the selection of
appropriate methods.
We requested and received public
comment on the above considerations
and on the proposal to allow the use of
appropriate methods such as those
found in SW–846 or other reliable
sources. One supportive commenter
believed the Agency had provided
sufficient guidance in the preamble to
the proposed rule on how to identify
appropriate methods. As discussed
below, a few commenters requested
additional guidance regarding the
selection of appropriate methods or had
questions regarding the approach.
One commenter requested that an
appropriate method definition be
codified in the regulations. The Agency
believes that codification of an
appropriate method definition would be
both very difficult and contrary to the
intent and purpose of this rule, given
the project-specific nature of
‘‘appropriate method selection’’ and the
wide variety of data collection
objectives that may be encountered. In
the paragraphs above, the Agency has
provided the key generic considerations
for appropriate method selection, which
together serve as our general definition
for an appropriate method, and
identified guidance sources, in the hope
that this information will assist readers
of this rule during the selection of
appropriate methods, regardless of
whether the methods are from SW–846
or other sources. In addition, since
publication of the proposed rule, ASTM
International published D 6956–03,
‘‘Standard Guide for Demonstrating and
Assessing Whether a Chemical
Analytical Measurement System
Provides Analytical Results Consistent
with Their Intended Use.’’ This
guidance document is not required by
any EPA program, but may be useful to
the regulated community during the
selection of appropriate methods and
during the evaluation of analytical
results. The document can be obtained
from ASTM by visiting its Web site at
https://www.ASTM.org or by writing to:
ASTM International, 100 Barr Harbor
Drive, P.O. Box C700, West
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Conshohocken, PA 19418–2959. EPA
also plans to continue to provide
training to affected entities on the
concepts of this rule and to support its
implementation. When using any
appropriate method, you should be able
to determine the analyte of concern
(e.g., the regulated constituent to be
measured), in the matrix of concern
(e.g., the physical substance which
might contain the regulated
constituent), at the level of concern (e.g.,
the regulated level of or the action level
for the analyte).
One commenter was concerned that
the regulated public might use other
methods that do not meet the QC
criteria in the SW–846 methods. The
Agency does not believe that this should
be a concern. The performance data and
QC criteria given in the SW–846
methods are only examples, and are not
requirements for analysis. The SW–846
example criteria may not be appropriate
for every analytical purpose.
Establishing QC criteria is a project
planning issue and not a method issue.
Methods should be adapted into
standard operating procedures (SOPs) to
meet QC criteria from systematic
planning documents, not the other way
around. Some analytical applications
may require more or less stringent QC
criteria than that given as examples in
the SW–846 methods, and it would be
contrary to promoting a PBMS approach
if all analyses using any methods are
expected to conform to the example
criteria published in SW–846 methods.
Sometimes, even when using an SW–
846 method, it may not be necessary to
fully meet its example performance
criteria because project-specific quality
objectives may not require evaluation of
the same performance indicators or the
criteria may not be appropriate to the
specific application. In keeping with a
PBMS approach and the goals of this
rule, performance criteria should be
determined on a project-specific basis
during the planning stage.
Another commenter was concerned
that some regulated entities might use
methods that were not originally
developed for environmental purposes,
and thus data validity may be suspect.
Provided that the method is appropriate
based on the factors discussed above
and in the proposed rule preamble, we
do not believe that this should be a
concern. If the data are suspect or
otherwise not of sufficient quality for
their intended use, then the method is
not appropriate, regardless of its source,
and thus the data are not acceptable for
demonstrating compliance. Regardless
of the original purpose or source of a
method, it can be an appropriate
method if it generates effective data,
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e.g., the data quality objectives and
performance criteria are met. Even an
SW–846 method may not be appropriate
for a particular application if it does not
generate effective data. In addition, the
application of method technologies from
other disciplines promotes the use of
innovative approaches and
technologies, which may benefit RCRArelated analyses. Finally, many of the
analytical techniques used today in
environmental analyses were initially
developed for other purposes.
One commenter agreed with EPA’s
approach to appropriate method
selection, but had comments regarding
the data quality objectives approach.
The commenter believed that the DQO
approach can be expensive and is not
usually used during small analytical
projects. In response, the Agency notes
that, when data are being used in
decision making involving two clearly
alternative conditions (e.g., compliance
vs. noncompliance with a regulatory
standard), the Agency’s recommended
systematic planning tool is the DQO
process. While there is no regulatory
obligation to use the DQO process, it is
the recommended planning approach
for many EPA data collection activities.
However, the DQO process may be too
complicated for some projects and is not
the only way to generate quality data
through systematic planning. It is
presented here in the MIR only as an
example of an approach involving
systematic planning. However, at a
minimum, the Agency recommends that
some form of systematic planning be
implemented for every data collection
effort in order to generate effective data,
and notes that such systematic planning
should also involve consideration of
cost. Systematic planning is a common
sense approach, designed to ensure that
the level of detail in planning is
commensurate with the importance and
intended use of the work and the
available resources.
One commenter supported EPA’s
proposed flexibility, but thought that
EPA should continue to use SW–846 as
the primary vehicle for making
recommendations regarding procedures
that will meet minimum quality
objectives for RCRA analyses. Thus, one
would not be required to use SW–846
methods, but could choose to use them
and be confident that they are
appropriate sampling and analysis
procedures, provided that they can be
demonstrated to meet project quality
objectives. Another commenter believed
that it would be unrealistic for a
regulated entity to agree to the use of
other methods if EPA has not approved
them. The commenter believed that
such approval would guarantee
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acceptance of the data, provided that the
method was properly followed.
First, it should be noted that there are
no ‘‘PBMS methods.’’ PBMS is a
regulatory approach where what has to
be accomplished is specified, rather
than how the monitoring is to be
conducted. Under such a system,
regulated entities are permitted to
employ any method that is technically
adequate to accomplish the compliance
demonstration. Regarding EPA’s
approval of PBMS, EPA has already
stated its objective to employ the
performance approach in its regulatory
and other monitoring programs to the
extent feasible. On October 6, 1997 (62
FR 52098–52100), EPA published in the
Federal Register its intent to adopt
PBMS agency-wide. Subsequently, on
May 8, 1998 (63 FR 25430–25438), EPA
published in the Federal Register a
notice of intent and request for
comment regarding its plans to reform
implementation of RCRA-related
monitoring by formally adopting PBMS
and by removing unnecessary required
uses of methods from the RCRA
regulations (part of PBMS).
EPA also believes that method
selection should be a project-specific
decision and therefore cannot
recommend or approve any methods—
even SW–846 methods—as always being
appropriate for any given application.
For that very reason, with this rule, EPA
removed the requirement to use SW–
846 methods, except when the methods
are the only ones capable of measuring
a particular property. Relying on the fact
that a method is contained in SW–846
does not guarantee that the method will
always generate effective data under any
situation. If the SW–846 method is not
an appropriate method for its intended
application, following it exactly could
generate erroneous data and could fail
to demonstrate compliance with the
RCRA requirements.
Second, EPA does not agree with the
recommendation that it categorically
state that any method is always an
effective means of demonstrating
compliance (with the exception of
methods for the analysis of methoddefined parameters) since the Agency
has no way of knowing that a particular
method is going to yield valid data in all
potential situations and it goes counter
to the performance approach which
requires that regulated entities
demonstrate compliance using data of
known and documented quality. The
Agency believes that it is up to the
individual regulated entity to decide
which methods are appropriate to use
for any given compliance demonstration
and that this determination should be
initiated during the project planning
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stage. When considering method
selection, the analytical performance
indicators are key to the specific project
goals that should be considered.
Examples of analytical performance
indicators that might be addressed
include method sensitivity and
selectivity, precision, bias, and
reproducibility. The data user may even
choose to revise method selection if
additional information gathered during
the project indicate that the initial
selection was not appropriate.
Therefore, method selection is a projectspecific activity implemented by the
regulated entity, and EPA’s only
concern is that the generated data be
effective for its purpose, regardless of
the method selection. The Agency does
recommend that a regulated entity seek
assistance from its regulating authority
should the regulated entity have
concerns regarding the use of any
particular method. EPA also notes that
guidance regarding demonstrating the
performance of a given analytical
method can be found in EPA-published
guidance documents (some of which are
listed above) and documents published
by other Agencies (e.g., ASTM).
One commenter was concerned
regarding how method performance
would be demonstrated under PBMS.
The commenter claimed that
implementation of a PBMS approach is
very difficult and that, for it to work,
there must be a ‘‘reference method’’ to
be used as a benchmark against which
to measure other methods.
EPA notes that the RCRA program
does not use reference methods. Many
different methods produce effective data
for a particular project, which are not
necessarily ‘‘equivalent,’’ but all could
be ‘‘applicable.’’ For example, there are
many analytical methodologies that can
be used in analyzing a particular metal
species (e.g., ICAP, AA). In selecting a
particular method for metal analysis, the
analyst will consider analytical costs,
accuracy and sensitivity needed,
freedom from potential interferences,
amount of sample required for an
analysis, reagents to be used, and other
factors in the overall process to select a
method that will yield effective data at
the lowest cost to the user. These factors
should be considered when evaluating
any method, including those published
in SW–846, and the user needs to
conduct the appropriate verifications to
demonstrate the appropriateness of any
method that is selected against its
intended application. There are a
number of approaches that can be used
to demonstrate that a method is valid for
a particular use. These include: use of
appropriate reference standards,
analysis of spiked samples, comparison
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34543
of results to results generated using a
method that employs a fundamentally
different measurement process and
would not be subject to the same
potential interferences, etc. For further
guidance in demonstrating method
validity, see the previously cited ASTM
document D 6956–03, ‘‘Standard Guide
for Demonstrating and Assessing
Whether a Chemical Analytical
Measurement System Provides
Analytical Results Consistent with their
Intended Use.’’
B. Public Comments Regarding Other
Approaches
As explained in section III.B of the
proposed rule preamble, EPA
considered several approaches to
promoting ‘‘method use’’ flexibility in
the RCRA regulations. We selected the
‘‘appropriate method’’ approach because
it is universally applicable to the subject
RCRA regulations. It also requires only
minimal revisions to the regulations for
implementation.
In addition, the option to use
‘‘appropriate methods’’ is not new to the
RCRA regulations. For example, use of
the TCLP, SW–846 Method 1311, is
required for determining whether a
waste is hazardous for the toxicity
characteristic (the TC). It generates an
extract (the leachate) which is subject to
a determinative analysis for comparison
with the TC regulatory limits. However,
the TCLP procedure does not require
specific analytical methods for the
leachate determinative analysis, nor
does it specify the use of even SW–846
methods in general for such analysis of
the leachate. It allows method flexibility
similar to that proposed by this rule by
stating in section 7.2.14: ‘‘The TCLP
extract shall be prepared and analyzed
according to appropriate analytical
methods.’’
Nevertheless, in the proposed rule
preamble, the Agency requested the
public’s opinion on two alternative
approaches that we considered during
development of this rulemaking.
1. As a variation to the ‘‘appropriate
method’’ approach described above,
should we remove mention of SW–846
methods as examples of potentially
appropriate methods from the subject
regulations?
2. In lieu of the ‘‘appropriate method’’
approach, should we instead add
specific measures of required
measurement system performance or
data quality objectives to each
regulation, such as done in the
comparable fuel rulemaking, and not
mention or require the use of an
appropriate method (including any SW–
846 methods)? In the proposed MIR, we
did not select this approach because it
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might require significant regulatory
changes with difficult to quantify
impacts.
Most of the commenters preferred that
EPA retain mention of SW–846 in the
regulations as examples of potentially
appropriate methods. However, some of
these commenters appeared to believe
that, by mentioning SW–846 methods as
examples, it meant that such methods
will always be appropriate for every
data collection effort addressed by the
regulation, and thus the performance of
other candidate methods should be
compared with the performance of the
similar SW–846 method. One
commenter wanted the Agency to
legally recognize that the SW–846
methods are appropriate methods under
the RCRA regulations.
The Agency strongly disagrees with
commenters that SW–846 methods
should be identified as always
appropriate. As explained in section
III.A of this rule, the determination of an
appropriate method should be made on
a project-specific basis and involves
consideration of various project-specific
objectives and criteria. As noted, an
appropriate method might be one
published by EPA in a different manual
from SW–846 or might be a method
published by a different government
agency, a voluntary standards setting
organization, or other well-known
scientific sources. Whether a method is
contained in SW–846 is not a primary
criterion for determining if a method is
appropriate. For example, there is a
common misconception that the
different SW–846 methods for sample
extraction all have the same extraction
efficiency, which is not the case at all,
since the methods were intended to be
appropriate for different applications.
Methods found in other publications
may be more appropriate based on the
project-specific considerations.
Regarding the addition of
performance criteria to the regulations,
a few commenters did prefer that such
criteria be added to the regulations.
However, these commenters did not
provide suggestions regarding how to
best resolve those instances when such
an approach might result in requiring
use of methods which are more accurate
or sensitive than necessary (with the
result that monitoring costs may
increase unnecessarily) or in other cases
would not yield data of a sufficient
quality to definitively determine if a
facility is in compliance with a
regulatory or permit level. Given these
impact issues and the project-specific
nature of what determines an
appropriate method, it would be
contrary to the purpose of this
rulemaking and very difficult to develop
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and implement performance criteria and
definitions that would be universally
applicable. EPA therefore decided
against adding criteria at this time to all
of the regulations. We strongly believe
that the appropriate method
determination should be made on a
project-specific basis by those familiar
with the purpose of the analysis and
should not be dictated by regulatory
definition. EPA believes that generic
performance criteria assigned by EPA
would not assure consistent application
of PBMS, but rather might discourage a
PBMS application and flexibility in
method selection and use. However, to
further evaluate this issue, the Agency’s
Forum on Environmental Measurements
(FEM) has formed an Action Team to
address issues related to
implementation of the performance
approach. It is anticipated that the
Action Team will address issues related
to data quality and data quality
documentation for use by all Agency
programs.
In conclusion, as a result of
consideration of all comments, we
decided to not add performance criteria
to the regulations. In addition, unlike
the proposal, we decided to not include
any references to SW–846 or ‘‘using
appropriate methods such as those
found in * * * SW–846’’ in the
regulatory provisions because those
references to SW–846 were unnecessary
and, based on public comment, the
regulated community may continue to
believe that SW–846 methods will
always be most appropriate.
C. Public Comments Regarding Impacts
From Removal of Required Uses of SW–
846 Methods
In the preamble to the proposed rule,
we summarized the expected impacts
on the regulated entities and the states,
and requested public comment on the
assumptions made in the analysis. We
also requested public comment on the
impact of this rule and how we might
promote its successful implementation.
The paragraphs to follow summarize our
impact assumptions and provide our
responses to some of the public
comments regarding these topics.
As a result of this final rule, you can
use any appropriate analytical test
method in demonstrating compliance
with the RCRA regulations, except for
those regulatory provisions involving
method-defined parameters. We believe
that this action will not significantly or
adversely impact the regulated
community or other potentially affected
parties because the Agency is not
adding any additional regulatory
requirements to the RCRA regulations,
but rather is clarifying and expanding
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the flexibility that regulated entities
have had in selecting appropriate
methods to employ to demonstrate
compliance whether or not such
methods were described in SW–846. By
making it clear that one may use any
appropriate method, regulated entities
may be able to cut the cost of
compliance monitoring by using less
expensive methods. Regulated entities
may continue to use SW–846 methods
to demonstrate compliance when it is
appropriate to do so, and thus
experience no impact from this
rulemaking. EPA will also continue to
publish and update SW–846 methods
and ensure their scientific soundness by
following peer review guidelines and
requesting public comment on the
methods through Federal Register
notices.
Thus, as we noted in section III.C of
the proposed rule preamble, the primary
impact of this rule will be better
analytical results (e.g., due to paying
better attention to method performance).
The Agency also anticipates a tendency
toward lower costs during compliance
with the affected RCRA regulations
because project planners may identify
methods that are potentially less costly
to use. Meanwhile, EPA also will
continue to provide training and utilize
our pool of Agency technical experts to
serve the public by answering questions
regarding the use of test methods during
RCRA-related compliance activities.
Also, a demonstration that another
method is appropriate is already
allowed within RCRA-related sampling
and analysis and will not involve much
more than what regulated entities
already should be doing. For example,
as the regulated entity, you should
already be setting method performance
goals in your Quality Assurance Project
Plan (QAPP), Sampling and Analysis
Plan (SAP), or other systematic planning
document and then evaluating
compliance with those goals based on
data quality indicators, including when
using SW–846 methods.
Regarding public concerns about the
comparability of data generated by
different methods for the same purpose,
we noted in the proposed rule preamble
that this practice is not new because
some regulations already allow the use
of more than one method. We also do
not believe that this should be a
concern, provided that any alternative
method is also an appropriate method as
defined above. Specifically, if both
methods generate effective data and
meet the data quality objectives of the
project, then results from both methods
will be acceptable for demonstrating
compliance. In addition, for situations
where trends or comparability are to be
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determined, measurement quality
objectives should be selected for use in
selecting methods to be used that will
ensure that, for whatever desired level
of difference one desires to determine,
the data will be suitable for the purpose.
This has always been EPA’s approach in
comparing data by different methods,
and it is not affected or changed by this
rule.
Some commenters preferred a more
prescriptive approach in the regulations
because method-specific requirements
remove the burden of method-selection
as it is believed that this translates into
lower costs and greater agreement
between permit writers and other
project participants who may not have
method-selection expertise. Because of
consequences of this approach, the
Agency believes it is undesirable. A
major problem with the prescriptive-or
mandated-methods approach is that it
can lead to data of poor quality which
can result in an incorrect assessment of
compliance. Another problem is that the
regulated community may not
systematically plan their data collection
efforts and thus not fully understand
their project-specific goals. Methodselection decisions should be project
specific and thus, specific methods
should not be required in the
regulations.
Some commenters also expressed
concern regarding the impact of this
rule on existing RCRA permits. RCRA
permits are typically effective up to ten
years. This rule will only effect new or
reissued permits, and only to allow
more flexibility in method selection.
Therefore, RCRA permits will not be
adversely impacted by this action.
Finally, this rule does not add new
information collection or reporting
requirements for regulated entities.
Section 260.22(i) (reporting
requirements for petitions to exclude
wastes) and §§ 264.13(b) and 265.13(b)
(reporting requirements for owners and
operators of hazardous waste
management facilities) provide
sufficient reporting requirements to
cover RCRA-related testing and analysis
documentation regarding the use of
other appropriate methods.
One commenter agreed, regarding
impact of the rule, that the MIR will
greatly benefit those situations where
repeated analyses are needed, such as
for a RCRA corrective action or for a
WAP for a hazardous waste treatment,
storage, or disposal facility (TSDF).
However, the commenter also believed
that smaller entities involved in waste
analyses, such as small quantity
generators (SQGs) will probably not
benefit from the MIR. For the reasons
given above, EPA believes that the
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impact of this rule will not be
significant for any generator, including
small quantity generators (SQGs),
largely because the flexibility of method
selection will provide better analytical
results at a lower cost. Project planners
and laboratories used by SQGs will
identify methods that are potentially
less costly and yet provide effective
data. EPA believes that the regulated
community will choose appropriate
methods based on cost and data quality
advantages, and therefore all regulated
entities, including SQGs, could benefit
from this rule.
One other commenter believed that if
PBMS is adopted, prior approval by the
State or other regulator of the method
should be mandatory. The commenter
argued that State reviewers are more
familiar with SW–846 methods and data
indicators and that a state’s
unfamiliarity with other methods might
mean the State may not perform a
timely review of the data.
As explained in the previous section,
EPA believes that method approval
prior to use would be contrary to the
intent and philosophy of the
performance concept and would negate
the positive impacts of this rule.
However, as also noted, the regulated
community can consult with their
regulating authority during the
identification of performance goals and
the selection of appropriate methods.
EPA appreciates the commenter’s
concern regarding potentially negative
impacts on the timely review of data. It
is true some delay in data review may
occur if the reviewer is not familiar with
the procedure. Nevertheless, review of
data should not be a new step in the
process since effected entities should
already be reviewing data indicators
from the SW–846 methods during
RCRA-related sampling and analysis.
Once the reviewer and user become
more familiar with a new method, less
time will be needed to perform an
equally thorough review. In the end, we
believe the benefits of modifying the
rules will far outweigh these potential
impacts on data review time through the
improvement of data effectiveness and a
decrease in other costs. To help mitigate
any potential negative impacts, we will
continue to provide training and our
staff are available to assist you during
all stages of the process.
Some commenters expressed a
concern that this action will impose an
additional resource burden on States. In
response, we note that the regulatory
changes in this rule are equivalent to or
less stringent than the existing Federal
regulations which they amend.
Therefore, authorized States are not
required to adopt and seek authorization
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34545
for this rulemaking within their
programs. If a State believes that
adoption may be too burdensome on
their resources, then they need not
adopt the revised regulations.
Nevertheless, we encourage the
adoption of these or similar revisions by
authorized States in order to promote
the national adoption of the
performance approach in environmental
regulations, permits, and monitoring. In
addition, if States choose to adopt these
revisions, the impact should not be
significant since they already conduct
method selection and data quality
reviews to determine compliance with
their testing and monitoring regulations.
Some commenters expressed a need
for communication and training to assist
in implementation of the MIR. We agree
and the Agency plans to continue to
provide education and training to
States, EPA Regions, and the regulated
community regarding the
implementation of this rule, through
such mechanisms as workshops, fact
sheets, and Internet training modules.
Over the past seven years, OSW has
offered program-specific training (e.g.,
‘‘Analytical Strategy for the RCRA
Program: A Performance-Based
Approach’’) for EPA Headquarters,
Regional, and State personnel involved
in RCRA activities that include
sampling and analysis. The Agency
plans to expand its performance
approach training program and offer
other courses on the evaluation of data
and permit writing from a PBMS and
effective data standpoint. These
communication and training efforts will
help ensure consistency in
implementation of this and other
Agency performance-based rules by the
States, Regions, and regulated
community and help limit any
associated costs.
IV. Regulatory Revisions Involving
Removal of SW–846 Requirements
In section IV of the proposed rule
preamble, EPA listed and discussed
each of the proposed regulatory
revisions which removed the
requirement to use SW–846 methods
and stated that appropriate methods
may be used. We requested public
comment on these individual regulatory
section revisions (e.g., comments
regarding any impacts on
implementation of each affected
regulation that we may have
overlooked) and in general did not
receive any significant negative
comments regarding the removal of the
SW–846 requirements from any of the
regulations. We are therefore finalizing
the removal of the requirement to use
SW–846 in those regulatory sections.
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In addition, we are finalizing
revisions to three conditional delistings
in part 261, appendix IX, which were
not included in the proposed rule, but
which, like those delistings that were
included in the proposal, unnecessarily
require the use of SW–846 methods. We
announced our intent to revise these
delistings in a memorandum to the
facilities and to the relevant EPA
Regional offices. We gave the entities
three weeks to comment on the
revisions. One of the affected companies
did not respond to the memorandum,
while the other two companies
responded, but did not have comments
regarding the revisions.
Therefore, we decided to proceed
with finalizing the revisions to these
three delistings. The revisions to the
conditional delistings are very similar to
the other conditional delistings. We did
not receive negative comments
regarding the general removal of
required uses of SW–846 in any of the
conditional delistings listed in the
proposed rule. We believe that these
revisions are fully consistent with EPA’s
original intent to make such changes to
any conditional delisting, or other
regulations, which unnecessarily
required the use of SW–846 methods for
analyses other than for required MDPs.
The additional conditional delistings
revised by this final rule are found in
Table 1 of appendix IX of part 261 and
address delisted wastes at the following
facilities:
—Bekaert Corp., Dyersburg, TN
—OxyVinyls, L.P., Deer Park, TX
—Tokusen USA, Inc., Conway, AR
In addition, since publication of the
proposed MIR, the Office of Federal
Register (OFR) revised its format for
incorporation by reference. Specifically,
the OFR requires that the MDP methods
incorporated by reference at § 260.11 be
specifically mentioned in the relevant
sections of the regulations, and not just
include referrals to § 260.11. Therefore,
in the conditional exclusion listings of
part 261, appendix IX, we included a
listing of the method-defined parameter
methods to replace our proposed
language stating that the methods listed
in § 260.11 must be used without
substitution when required. Those
methods must be used as applicable to
the particular delisting.
Finally regarding the conditional
delistings, we are taking this
opportunity to make several editorial
corrections to Tables 1, 2 and 3 of
appendix IX of part 261, which in no
way substantially change or remove any
requirements. We are removing repeats
of the Bekaert Corp., Dyersburg, TN,
conditional delisting from Tables 2 and
3 of appendix IX of part 261 because
those entries were added to the tables in
error. The Bekaert Corp. conditional
delisting is for an F006 waste, which is
from a non-specific source, and
therefore the delisting only belongs in
Table 1, which lists wastes excluded
from non-specific sources (i.e., ‘‘F’’
coded listed wastes). Tables 2 and 3 of
appendix IX of part 261 are meant to
only list the conditional delistings of
wastes excluded from specific sources
(Table 2, i.e., ‘‘K’’ coded listed wastes)
or from commercial chemical products,
off-specification species, container
residues, and soil residues thereof
(Table 3, i.e., ‘‘P’’ and ‘‘U’’ coded listed
wastes). Similarly, we are removing the
OxyVinyls, Dear Park, TX, delisting
from Table 1 and adding it to Table 2
of appendix IX. This is necessary
because the OxyVinyls’ delisting
addresses K017, K019, and K020 wastes
and was incorrectly placed in Table 1.
Since these are changes that do not
affect the implementation of the
regulations, or add new or remove
existing regulatory requirements, the
Agency is providing notice of the
changes without opportunity for
comment.
Table 2 lists the regulatory revisions
finalized by this rule to remove the
requirement to use SW–846 methods
and allow the flexibility to use other
appropriate methods. As noted in the
previous section of this preamble, the
proposed references to ‘‘using
appropriate methods such as those
found in * * * SW–846’’ is not being
included in the final regulation because
the Agency decided that those
references to SW–846 were unnecessary
and because the regulated community
may continue to believe that SW–846
methods will always be most
appropriate. Finally, we corrected our
proposed revision to
§ 261.35(b)(2)(iii)(B) by adding the
relevant data from Table 1 of Method
8290 to the regulatory text so that
Method 8290 (which contained the table
but is not an MDP method) no longer
has to be incorporated by reference. In
the proposed rule, § 261.35(b)(2)(iii)(B)
read as follows: ‘‘Not detected means at
or below the lower method calibration
limit (MCL) in SW–846 Method 8290,
Table 1. Other appropriate methods
from other reliable sources may be used
provided that these criteria are met.’’ In
the final rule, we copied the relevant
data from Table 1 directly into
§ 261.35(b)(2)(iii)(B) and so it is no
longer necessary to mention Method
8290.
TABLE 2.—REVISIONS TO RCRA REGULATIONS TO REMOVE REQUIRED USES OF SW–846 METHODS
Regulation
Affected topic or program
§ 260.22(d)(1)(i) ........................................................................
Appendix IX to part 261 ...........................................................
§§ 261.35(b)(2)(iii)(A) and (B) ..................................................
§ 261.38(c)(7) ...........................................................................
§§ 264.1034(d)(1)(iii), 264.1063(d)(2), 265.1034(d)(1)(iii), and
265.1063(d)(2).
§§ 265.1084(a)(3)(iii) and (b)(3)(iii), and 265.1084(a)(3)(ii)(C),
(b)(3)(ii)(C), and (c)(3)(i).
§§ 266.100(d)(1)(ii) and (g)(2), and 266.102(b)(1) ...................
§ 266.106(a) ..............................................................................
§§ 266.112(b)(1) and (b)(2)(i) ...................................................
Appendix IX, part 266 ..............................................................
§§ 270.19(c)(1)(iii)
and
(iv),
270.22(a)(2)(ii)(B),
270.62(b)(2)(i)(C) and (D), 270.66(c)(2)(i) and (ii).
This rule also revises the
incorporation by reference of SW–846 in
§ 260.11 so that the paragraph only
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Petitions to exclude waste from a particular facility.
Wastes excluded under §§ 260.20 and 260.22.
Deletion of certain waste codes following equipment cleaning.
Comparable/syngas fuel exclusion.
Air emission standards for process vents and equipment leaks.
Air emission control requirements for tanks, surface impoundments, and containers.
Hazardous wastes burned in boilers and industrial furnaces (BIFs).
Control of metal emissions at BIFs.
Residues from burning of wastes in BIFs.
Methods Manual for BIF regulations.
Part B information and trial burn plan requirements for incinerators and BIFs.
includes SW–846 methods that are
required for method-defined parameters.
Therefore, for each section where we
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removed the requirement to use only
SW–846 methods, we also removed the
SW–846 incorporation by reference.
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Prior to this rule, all methods of SW–
846 were incorporated by reference at
§ 260.11 ‘‘when used’’ within the RCRA
regulations. All of SW–846 had to be
incorporated by reference because some
RCRA regulations required in general
the SW–846 methods, e.g., the delisting
regulations at § 260.22(d)(1)(i). The
required methods had to be
incorporated by reference because their
full text is too lengthy for publishing
directly in the regulations and the
methods are readily available to the
public in the SW–846 manual. As a
result of this rule, we are limiting the
requirement to use SW–846 methods to
when the methods analyze required
method-defined parameters. Therefore,
we revised § 260.11 to remove the
incorporation by reference of all SW–
846 methods, except those SW–846
methods that may be required for the
analyses of method-defined parameters.
Those methods will remain
incorporated by reference when used for
method-defined parameters and
required by the RCRA regulations.
It is important to note that, while a
method is listed in § 260.11 because it
is used for analysis of a method-defined
parameter, it also may be used for nonmandatory purposes. In those cases
where the method is required by a
specific regulation and is listed in
260.11, it is a method-defined
parameter. For example, Method 9010C,
‘‘Total and Amenable Cyanide:
Distillation,’’ and Method 9012B, ‘‘Total
and Amenable Cyanide (Automated
Colorimetric, with Off-line Distillation)’’
are required under § 268.44, the
universal treatment standards of the
land disposal restrictions regulations,
and are listed in § 260.11 as required by
§ 268.44. In that case, the methods
cannot be substituted. However, in other
circumstances, these two methods may
be used when they are not required by
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their regulations (e.g., during delistings)
and in those cases they will only be
considered appropriate methods and not
MDPs. It is the application of a method
in a regulation that determines whether
a method is being used to analyze a
required method-defined parameter—
not simply whether the method is listed
in § 260.11.
The SW–846 methods that remain as
incorporated by reference in § 260.11
are listed in Table 3. The final list is
different from that proposed in that
Methods 3542 (‘‘Extraction of
Semivolatile Analytes Collected Using
Method 0010 (Modified Method 5
Sampling Train)’’) and 5041A
(‘‘Analysis for Desorption of Sorbent
Cartridges from Volatile Organic
Sampling Train (VOST)’’) are no longer
included. The methods were removed
because they are currently not used as
method-defined parameters under the
RCRA program.
TABLE 3.—SW–846 METHODS TO REMAIN IN § 260.11
SW–846
method
Chapter
location
0010 ..........
0011 ..........
0020 ..........
0023A ........
Ten
Ten
Ten
Ten
..........
..........
..........
..........
0030 ..........
0031 ..........
0040 ..........
0050 ..........
0051 ..........
0060 ..........
0061 ..........
1010A ........
1020B ........
1110A ........
1310B ........
1311 ..........
1312 ..........
1320 ..........
1330A ........
9010C ........
9012B ........
9040C ........
9045D ........
9060A ........
9070A ........
9071B ........
9095B ........
Ten ..........
Ten ..........
Ten ..........
Ten ..........
Ten ..........
Ten ..........
Ten ..........
Eight ........
Eight ........
Eight ........
Eight ........
Eight ........
Six ...........
Six ...........
Six ...........
Five ..........
Five ..........
Eight ........
Six ...........
Five ..........
Five ..........
Five ..........
Six ...........
Method title
Modified Method 5 Sampling Train.
Sampling for Selected Aldehyde and Ketone Emissions from Stationary Sources.
Source Assessment Sampling System (SASS).
Sampling Method for Polychlorinated Dibenzo-p-Dioxins and Polychlorinated Dibenzofuran Emissions from Stationary
Sources.
Volatile Organic Sampling Train.
Sampling Method for Volatile Organic Compounds (SMVOC).
Sampling of Principal Organic Hazardous Constituents from Combustion Sources Using Tedlar Bags.
Isokinetic HCl/Cl 2 Emission Sampling Train.
Midget Impinger HCl/Cl2 Emission Sampling Train.
Determination of Metals in Stack Emissions.
Determination of Hexavalent Chromium Emissions from Stationary Sources.
Pensky-Martens Closed-Cup Method for Determining Ignitability.
Setaflash Closed-Cup Method for Determining Ignitability.
Corrosivity Toward Steel.
Extraction Procedure (EP) and Structural Integrity Test.
Toxicity Characteristic Leaching Procedure.
Synthetic Precipitation Leaching Procedure.
Multiple Extraction Procedure.
Extraction Procedure for Oily Wastes.
Total and Amenable Cyanide: Distillation.
Total and Amenable Cyanide (Automated Colorimetric, with Off-line Distillation).
pH Electrometric Measurement.
Soil and Waste pH.
Total Organic Carbon (TOC).
n-Hexane Extractable Material (HEM) for Aqueous Samples.
n-Hexane Extractable Material (HEM) for Sludge, Sediment, and Solid Samples.
Paint Filter Liquids Test.
Please note that we are not adding any
new methods to § 260.11—each method
listed in Table 3 is already a part of SW–
846 and was incorporated by reference
during previous rulemakings. For each
method retained as incorporated by
reference, we are listing in § 260.11 the
promulgated version of the method
which was last incorporated by
reference and thus which must be used
during regulatory compliance.
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In addition, since proposal of this
rule, the Office of Federal Register
(OFR) has revised the format of
incorporation by reference sections
within the Federal regulations, for
instance, to include information
regarding those regulatory sections or
parts that specify use of the methods.
We revised § 260.11(a) to reflect this
new format.
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V. Editorial Corrections to SW–846
References in the RCRA Testing and
Monitoring Regulations
In section V of the preamble to the
proposed rule, the Agency proposed to
correct inaccurate references to SW–846
(some of which are logical outgrowths to
the revision to § 260.11), and to clarify
method selection flexibility in the RCRA
regulations. We did not receive any
negative comments regarding that
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section of the proposed rule and thus
are finalizing the editorial corrections,
as proposed.
In addition, we are correcting certain
regulations so that they include the
appropriate suffix of the SW–846 MDP
method required by them. As a result of
these corrections, the method number in
the regulation includes the suffix and
matches the respective method number
and suffix listed in § 260.11.
Table 4 lists and summarizes the
editorial corrections to the RCRA
regulations made by this final rule.
TABLE 4.—CORRECTIONS, CLARIFICATIONS OR REMOVALS
Regulation
Text correction, clarification, or removal
§ 258.28(c)(1)—Liquids restrictions ..........................................
Correction to add ‘‘incorporated by reference in § 260.11’’ after ‘‘Paint Filter Liquids Test,’’ and addition of the suffix ‘‘B’’ to the method number ‘‘9095.’’
Removal of footnote 1 to the table, which contains unnecessary references to
SW–846.
Clarification regarding the use of other appropriate methods by removing the
‘‘Suggested Methods’’ and ‘‘PQLs (µg/L)’’ columns, removing footnotes 1, 5
and 6 and revising and renumbering the remaining footnotes, as appropriate.
Clarification that equivalent methods will be added to § 260.11, instead of just
added to SW–846.
Removal of unnecessary reference to SW–846.
Appendix I to part 258—Constituents for detection monitoring
Appendix II to part 258—List of inorganic and organic hazardous constituents.
§ 260.21(d)—Petitions for equivalent methods ........................
§ 260.22(d)(1)(i)—Petitions to amend part 261 to exclude a
waste produced at a particular facility.
§§ 261.3(a)(2)(v), 279.10(b)(1)(ii), 279.44(c), 279.53(c), and
279.63(c)—Rebuttable presumption for used oil.
§ 261.22(a)(1)—Characteristic of corrosivity ............................
Appendix I to part 261—Representative sampling methods ...
Appendix II to part 261—Method 1311 Toxicity Characteristic
Leaching Procedure (TCLP).
Appendix III to part 261—Chemical analysis test methods .....
§§ 264.190(a) and 265.190(a)—Applicability ...........................
§ 264.314(c) and § 265.314(d)—Special requirements for bulk
and containerized liquids.
§§ 264.1034(f) and 265.1034(f)—Test methods and procedures.
Appendix IX to part 264—Ground-water monitoring list ..........
§ 265.1081—Definitions ............................................................
Appendix IX to part 266—Methods manual for compliance
with BIF regulations.
§ 268.40(b) and table—Applicability of treatment standards ...
§ 268.44, table—Variance from a treatment standard .............
§ 268.48, table—Universal treatment standards ......................
Appendix IX to part 268—Extraction Procedure (EP) Toxicity
Test Method and Structural Integrity Test (Method 1310).
VI. Action To Withdraw the Reactivity
Interim Guidance From SW–846
Chapter Seven and Remove Required
SW–846 Reactivity Analyses and
Threshold Levels From Conditional
Delistings
In section VI of the preamble to the
proposed rule, the Agency proposed to
withdraw the reactivity interim
threshold levels and reactive cyanide
and sulfide methods from Chapter
Seven of SW–846 and from certain
conditional delistings found in
appendix IX to 40 CFR part 261. EPA
proposed these actions based on
conclusions it reached and announced
in an April 21, 1998 memorandum, a
copy of which is available in the docket
to this rulemaking, in which EPA
addressed concerns about the
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Removal of unnecessary references to SW–846.
Addition of the suffix ‘‘C’’ to method number ‘‘9040.’’
Removal of unnecessary references to SW–846.
Removal of text in Appendix II to part 261; appendix reserved.
Removal of text in Appendix III to part 261; appendix reserved.
Addition of the suffix ‘‘B’’ to method number ‘‘9095.’’
Addition of the suffix ‘‘B’’ to method number ‘‘9095.’’
Clarification that direct measurement is allowed to resolve disagreements regarding concentration estimates, and removal of unnecessary references to SW–
846.
Clarification regarding the use of other appropriate methods by removing the
‘‘Suggested Methods’’ and ‘‘PQLs (µg/L)’’ columns and removing footnotes 1, 5
and 6 and revising and renumbering the subsequent footnotes, as appropriate.
Correction to SW–846 reference in definition of ‘‘waste stabilization process.’’
Corrections to reflect removal of SW–846 methods from the BIF Methods Manual
on June 13, 1997 and clarification in existing guidance regarding use of other
appropriate methods and SW–846.
Addition of the suffix ‘‘B’’ to method number ‘‘1310,’’ addition of the suffix ‘‘C’’ to
method number ‘‘9010,’’ and addition of the suffix ‘‘B’’ to method number
‘‘9012.’’
Addition of the suffix ‘‘C’’ to method number ‘‘9010’’ and the addition of the suffix
‘‘B’’ to method number ‘‘9012.’’
Addition of the suffix ‘‘C’’ to method number ‘‘9010’’ and addition of the suffix ‘‘B’’
to method number ‘‘9012.’’
Addition of the suffix ‘‘B’’ to method number ‘‘1310.’’
effectiveness of the reactivity analysis
procedures (see the proposed rule
preamble for details regarding the
content of this memo and its history).
(See the April 21, 1998 memorandum at
https://www.epa.gov/SW–846/ for
detailed information regarding NEIC’s
concerns and EPA’s conclusions.) EPA
consequently withdrew the July 1985
guidance through the aforementioned
April 21, 1998 memorandum. To
summarize, EPA concluded that the
guidance had the following significant
problems:
(1) The test conditions evaluate a
single pH condition and not the range
of pH conditions (2 to 12.5) specified in
the reactivity regulation;
(2) The test conditions do not
adequately recover the analyte and thus
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the tests predict low percentages of
analyte releases in the waste;
(3) The mismanagement scenario and
test conditions are not correctly scaled
between each other; and
(4) The mismanagement scenario of
an open pit is not the only exposure of
concern and may not represent a
plausible worst case scenario.
EPA received comments from eleven
different commenters regarding this
topic. You will find a background
document containing our complete
responses to all relevant public
comments in the docket to this rule,
docket number RCRA–2002–0025, at the
location listed above under ADDRESSES.
Three commenters supported the
removal of the reactivity test
procedures, stating that they believed
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the test and guidance is flawed and that
appropriate waste classifications can be
made in the absence of guidance. On the
other hand, three other commenters
opposed the removal of the reactivity
test procedures. One of these
commenters stated that there are a
number of concerns about the technical
reasons for removal of the procedures,
and believed that these warrant
reconsideration of the proposed deletion
of the guidance. In reviewing these
concerns, the Agency found that the
commenter may be misreading the
Agency’s basis for deletion of the
guidance from SW–846. The commenter
was concerned both about the impact of
certain pH testing conditions and the
use of Henry’s Law in the guidance.
However, these topics were not the
reasons for withdrawing the guidance
from SW–846. The Agency will
investigate the commenter’s concerns
regarding pH testing conditions and
Henry’s Law as it develops revised
guidance. Another one of the
commenters asserted that the narrative
criteria alone can be used for
classification of high concentration
cyanide wastes, but that additional
guidance is needed for classifying lower
level cyanide-bearing wastes. The other
commenter understood the difficulties
associated with the reactivity method
guidance, but believed that the
regulated community needed something
other than the ‘‘honor system’’ to
classify these reactive wastes.
The remaining five commenters had
general concerns about making the
reactivity characteristic determinations,
but did not specifically support or
oppose deletion of the tests or threshold
levels. Four commenters out of the total
of eleven commenters requested that
EPA replace the deleted tests with other
method guidance.
In response to all comments, the
Agency is currently reviewing several
test methods for possible inclusion in
SW–846 as methods for characterizing
cyanide-bearing wastes. However, the
Agency still believes it inappropriate to
retain the reactive cyanide and reactive
sulfide methods in SW–846 for the
reasons presented in the proposed rule
preamble and listed above. Regarding
the characteristic of reactivity, regulated
parties have always been responsible for
complying with the regulation at
§ 261.23—Characteristic of reactivity,
which does not require any particular
test methods for the characterization.
Therefore, generators and other persons
can use other appropriate methods or
process knowledge in determining
whether a particular waste is hazardous
due to its reactivity.
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VII. Clarifications to Corrosivity and
Ignitability Hazardous Waste
Characteristics
In sections VII.A and VII.B of the
preamble to the proposed rule, the
Agency proposed revisions to the
corrosivity characteristic and the
ignitability characteristic testing
requirements. The proposed revisions
included changes to references to ASTM
standards and SW–846 methods. We
considered these revisions to be nonsubstantive updates of the methods
presently used in the regulations and we
believed the revisions would not affect
which wastes are determined to be
hazardous based on the characteristics.
We requested public comment on each
of the proposed revisions. Significant
comments and our responses are
provided below.
A. Revision to § 261.22(a)(2) To Clarify
That SW–846 Method 1110A Is the SW–
846 Standardized Version of the NACE
Standard Specified for Corrosivity
Characteristic Testing
In section VII.A of the preamble to the
proposed rule, EPA addressed proposed
revisions to the corrosivity
characteristic testing requirements,
which included a clarification to
§ 261.22(a)(2). Section 261.22(a)(2)
defines the hazardous waste
characteristic of corrosivity for a liquid
which corrodes steel. The required test
method is identified as ‘‘the test method
specified in NACE * * * Standard TM–
01–69 as standardized in * * * SW–846
* * *’’ As explained in the May 19,
1980 regulations (see 45 FR 33084)
which added § 261.22 to the RCRA
regulations, EPA standardized the
NACE Standard TM–01–69 in SW–846.
As also explained in the background
document to the corrosivity
characteristic of the 1980 regulations,
NACE Standard TM–01–69 describes a
simple immersion test to determine the
rate of corrosion. However, the
procedure described in the background
document, in fact, was not completely
standardized because it was designed to
test the suitability of metals for a variety
of uses. As a result, a comment was
submitted at that time which expressed
concern with the incomplete
standardization of the NACE Standard
which allowed variation in test
conditions. EPA agreed and, in response
to the comment, put a standardized
version of the method in SW–846 so
that the procedure more clearly defined
the appropriate test conditions. At the
time, we did not specify which test
method of SW–846 included the
standardized version of the NACE
method. This SW–846 method has
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always been Method 1110 (now Method
1110A as of Update IIIB), ‘‘Corrosivity
Toward Steel.’’ Therefore, in the
proposed MIR, we proposed adding the
number of this method to § 261.22(a)(2)
for clarification of which SW–846 test
method is the standardized version of
NACE. This revision to § 261.22(a)(2)
does not represent a change to the
characteristic.
Three commenters addressed this
section of the proposed MIR. Two of
these commenters explicitly supported
the clarification in § 261.22(a)(2) that
SW–846 Method 1110A, ‘‘Corrosivity
Toward Steel,’’ is the standardized
version of the NACE Standard TM–01–
69. The other commenter did not
comment on the proposed revision, but
instead requested that EPA address a
unrelated concern regarding the content
of Method 1110A. None of the
commenters disagreed with the Agency
statement that the revisions were nonsubstantive.
Regarding SW–846 Method 1110A,
the commenter believed that the method
significantly differed from the
corresponding Department of
Transportation (DOT) corrosivity
method. Specifically, Method 1110A
suggests that a 24-hour test duration be
used, while the DOT method indicates
use of a longer test period. The
commenter requested that EPA either
clarify this difference or amend the
regulations to allow the use of DOT’s
comparable corrosivity characteristic
procedure, as set out in 49 CFR
173.137(c)(2), as an alternative test
method for corrosivity under the
hazardous waste regulations.
First, EPA notes that the test duration
time in Method 1110A was not
addressed or proposed for revision by
the MIR. The MIR only proposed to
clarify that Method 1110A is ‘‘the test
method * * * standardized * * * in
SW–846’’ for the corrosivity
characteristic determination. The
commenter does not appear to disagree
with the proposed clarification. Because
the Agency did not take comment, or
even raise an issue, with the test
duration time, we believe it
inappropriate to address this provision
in this final rule. Nevertheless, the
Agency plans to evaluate the
commenter’s concerns to determine if
future regulatory changes are warranted.
Therefore, in response to the
comments submitted, the Agency is
finalizing the regulatory revision
whereby Method 1110A will be
specified in § 261.22(a)(2). It is not
necessary to also reference the NACE
Standard TM–01–69 in the regulatory
text. The NACE method was used to
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initially develop Method 1110A and the
two methods are not identical.
B. Revisions to § 261.21(a)(1) To Remove
an Unnecessary Referral to Method
Equivalency Petitions; and an
Explanation Regarding the Decision To
Not Revise the Regulation To Include
the Updated ASTM Standards and
References to Methods 1010A and
1020B as Proposed
In section VII.B of the preamble to the
proposed rule, the Agency addressed
proposed revisions to the ignitability
characteristic testing requirements in
§ 261.21(a)(1). Section 261.21(a)(1) of
the RCRA regulations defines the
hazardous waste characteristic of
ignitability as a liquid which has a flash
point less than 60 °C (140 °F) as
determined by the use of ASTM
Standard D 93–79 or D 93–80 (PenskyMartens Closed Cup Tester) or ASTM
Standard D 3278–78 (Setaflash Closed
Cup Tester). Since publication of the
regulation, the ASTM Standard has been
revised. However, before proposing to
replace the ASTM Standard now in the
regulation with the newer versions D
93–99c and D 3278–96, EPA compared
the newer versions of the test protocol
with the older versions of the protocol
and found only non-substantive
differences. Therefore, EPA proposed
and requested comment on replacing
the older versions of the ASTM
Standard in § 261.21(a)(1) with the more
recent versions. In addition, although
ASTM Standard D 93–00 is newer than
D 93–99c, EPA proposed that D 93–99c
replace D 93–80 because EPA found that
D 93–00 differed in a possibly
substantial manner from D 93–80 and, if
it were to be specified instead of D 93–
99c, characteristic results may be
significantly affected. Specifically, we
found that the D 93–00 version specifies
different sample container volumes for
different sample types. It requires that
all matrices, except residual fuel oil, be
collected in containers not more than
85% or less than 50% full. This revision
may significantly affect the
characteristic results, since the potential
to lose flammable volatile constituents
will be greater from sample containers
that may now have as much as 50%
headspace. The Agency requested
comment on this evaluation.
Finally, the Agency proposed to
revise § 261.21(a)(1) to clarify that the
ASTM standards for ignitability
characteristic determinations are used
and referenced by SW–846 Methods
1010A and 1020B. The Agency believed
these revisions to § 261.21(a)(1) to be
non-substantive and that the changes
would not affect which wastes are
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determined to be hazardous based on
the characteristic.
Five commenters addressed this
section of the proposed MIR. Two
commenters supported EPA’s proposal
to update the references to ASTM
standards in § 261.21(a)(1). Two other
commenters had general concerns about
the ignitability characteristic and the
ASTM standards, but did not appear to
specifically support or oppose the
replacements. Only one commenter
commented on revising § 261.21(a)(1) to
clarify that the ASTM standards for the
ignitability characteristic are used and
referenced by SW–846 Methods 1010A
and 1020B. The commenter supported
the regulatory revision.
Regarding ASTM Standards D 93–99c
and D 93–00, the two commenters that
supported updating the references
agreed with EPA that D 93–99c and D
93–00 could yield different results and
therefore, different conclusions as to
whether or not a waste would be
identified as hazardous. The two
commenters that disagreed with the
Agency’s conclusion regarding D 93–00
maintained that the potential to lose
volatile compounds also existed in the
1999 version. One of these commenters
noted that an even newer version than
D 93–00 was now available from ASTM,
namely D 93–02. The commenter
recommended that the Agency study
that standard for any significant
differences.
The Agency has considered all of the
comments and decided to retain the
existing ASTM regulatory standards and
not replace them with the newer
versions at this time. The Agency agrees
with the commenter who suggested that
EPA further study and review the new
versions of the ASTM standards. Both
newer versions of D 93 require that
certain ASTM sampling procedures be
used, which are unnecessarily
prescriptive and often inapplicable to
hazardous waste collection. The newer
version of D 93 may also promote
potential problems with requirements
for sampling and automated test
equipment. As a result, the Agency
believes that a more detailed evaluation
is warranted. In addition, the Agency
believes that, although the newer
versions of D 93 allows for automated
test equipment, including the use of an
electric igniter which may save time, a
rigorous comparison of the electrical
igniter versus the flame igniter should
be conducted.
In addition, the Agency decided to
not finalize the addition of references to
Methods 1010A and 1020B in the
regulations as proposed, but rather
Methods 1010A and 1020B were revised
as part of Final Update IIIB (final today
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as part of this rule, see section VIII),
whereby all method text was replaced
with direct references to the ASTM
standards listed in § 261.21(a)(1).
Finally, as proposed regarding
§ 261.21(a)(1), we are removing that
portion of the last sentence which refers
to the equivalent test method
demonstration. This information is
adequately addressed in §§ 260.20 and
260.21. It is not necessary to repeat the
information regarding method
equivalency petitions in each section of
a RCRA regulation which requires use of
a specific test method(s). Also, this
revision is consistent with similar
sections on testing in part 261 and other
parts of the RCRA regulations.
VIII. Availability of Final Update IIIB
and Status of Final Update IV to SW–
846
SW–846 is a guidance document that
changes over time as new information
and data are developed. On October 30,
2002, we proposed to revise several
methods and chapters of SW–846 and
release these revisions as Update IIIB to
the Third Edition of SW–846. To date,
EPA has finalized Updates I, II, IIA, IIB,
III, and IIIA to the Third Edition of the
SW–846 manual. On May 8, 1998 (see
63 FR 25430) and on November 27, 2000
(see 65 FR 70678), we also announced
the availability of Draft Update IVA and
IVB, respectively, which we published
for guidance purposes only.
As part of this rule, we are finalizing
Update IIIB. The Methods Team Web
site at https://www.epa.gov/SW–846 has
been revised to remove Proposed
Update IIIB and include an integrated
electronic version of SW–846 which
incorporates the final version of that
update. In the near future after
publication of this rule, Draft Updates
IVA and IVB will be replaced by Final
Update IV and its availability will be
announced by a Federal Register notice.
The revised methods of Update IIIB
are used for method-defined parameters
and thus, any required uses of those
methods will remain in the RCRA
regulations. Therefore, we revised
§ 260.11 to include the Update IIIB
methods.
In the proposed rule preamble, we
also requested comments on certain
parts of the Update IIIB methods and
chapters. We did not consider
comments on the other sections or parts
of the methods or chapters because
those portions were not proposed for
revision. Most of the comments
concerned the removal of the reactivity
guidance methods from Chapter Seven
and updating the ASTM standards.
Those comments are addressed in
previous sections of this preamble. The
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Agency received a few other comments
regarding the documents contained in
Proposed Update IIIB. The docket to this
rule (RCRA–2002–0025) contains a
background document with our
responses to all the comments
submitted. The responses also identify
any revisions made to the methods due
to the comments.
Table 5 provides a listing of the four
chapters and eleven methods in Final
Update IIIB. The method numbers in the
table reflect the appropriate method
revision letter suffix (e.g., A, B, C, etc.).
These suffixes were not always reflected
in the RCRA regulations themselves,
e.g., the regulations cited the method
number without a suffix. The relevant
regulations revised by today’s rule do
reflect the latest suffix. Accordingly,
this final rule identifies the latest
promulgated version of the methods that
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remain as incorporated by reference at
§ 260.11 in the RCRA regulations.
During compliance with those
regulations, the regulated community
must only use the latest promulgated
revision of the methods as indicated in
§ 260.11, i.e., the regulated community
must only use the version of the method
cited by § 260.11.
TABLE 5.—FINAL UPDATE IIIB METHODS AND CHAPTERS
Chapters or method number
Method or chapter title
Chapter Five .......................................................
Chapter Six .........................................................
Chapter Seven ....................................................
Chapter Eight ......................................................
1010A ..................................................................
1020B ..................................................................
1110A ..................................................................
1310B ..................................................................
9010C .................................................................
9012B ..................................................................
9040C .................................................................
9045D .................................................................
9060A ..................................................................
9070A ..................................................................
9095B ..................................................................
Note: A suffix of ‘‘A’’ in the method
number indicates revision one (the method
has been revised once). A suffix of ‘‘B’’ in the
method number indicates revision two (the
method has been revised twice). A suffix of
‘‘C’’ in the method number indicates revision
three (the method has been revised three
times).
IX. Addition of Method 25A to
§§ 264.1034(c)(1)(ii) and (iv) and
265.1034(c)(1)(ii) and (iv)
In section IX of the preamble to the
proposed rule, the Agency proposed to
revise §§ 264.1034(c)(1)(ii) and (iv) and
§§ 265.1034(c)(1)(ii) and (iv) to allow
the use of Method 25A, as well as
Method 18, during analyses in support
of air emission standards for process
vents and/or equipment leaks at
hazardous waste management facilities.
All comments supported these revisions
and therefore we finalized these
changes, as proposed.
X. Removal of Requirements From
§§ 63.1208(b)(8)(i) and (ii) in the
NESHAP Standards To Demonstrate
Feedstream Analytes Are Not Present at
Certain Levels
In section X of the preamble to the
proposed rule, the Agency proposed to
remove the requirements for analytical
DQOs (e.g., 80% upper confidence
limit) for feedstream analyses found in
§§ 63.1208(b)(8)(i) and (ii) that were
previously promulgated in the National
Emission Standards for Hazardous Air
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Miscellaneous Test Methods.
Properties.
Characteristics Introduction and Regulatory Definitions.
Methods for Determining Characteristics.
(Referral to) Pensky-Martens Closed Cup Method for Determining Ignitability.
(Referral to) Setaflash Closed Cup Method for Determining Ignitability.
Corrosivity Toward Steel.
Extraction Procedure (EP) Toxicity Test Method and Structural Integrity Test.
Total and Amenable Cyanide: Distillation.
Total and Amenable Cyanide (Automated Colorimetric, with Off-line Distillation).
pH Electrometric Measurement.
Soil and Waste pH.
Total Organic Carbon.
n-Hexane Extractable Material (HEM) for Aqueous Samples.
Paint Filter Liquids Test.
Pollutants (NESHAP) for Hazardous
Waste Combustors on September 30,
1999. All comments supported these
revisions and therefore we are finalizing
these changes, as proposed.
XI. Status of the RCRA Waste Sampling
Draft Technical Guidance
In section XI of the preamble to the
proposed rule, we announced the
availability of a stand-alone sampling
guidance document entitled, ‘‘RCRA
Waste Sampling Draft Technical
Guidance.’’ We intended to replace the
original sampling guidance version of
Chapter Nine found in EPA publication
SW–846 with this new document. We
requested comment on the guidance.
The Agency received a number of
comments which are still under review
and consideration. This additional
review of the document will help us
improve the guidance and ensure that it
is most useful in its final form.
Therefore, we are not at this time
issuing a final version of the sampling
guidance. Once we complete our review
and evaluation of the comments, we
will revise the document as appropriate
and announce its availability in the
Federal Register.
XII. State Authorization Procedures
A. Applicability of Federal Rules in
Authorized States
Under section 3006 of RCRA, EPA
may authorize qualified states to
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administer the RCRA hazardous waste
program within the state. Following
authorization, the state requirements
authorized by EPA apply in lieu of
equivalent Federal requirements and
become Federally enforceable as
requirements of RCRA. EPA maintains
independent authority to bring
enforcement actions under RCRA
sections 3007, 3008, 3013, and 7003.
Authorized states also have
independent authority to bring
enforcement actions under state law. A
state may receive authorization by
following the approval process
described in 40 CFR part 271. 40 CFR
part 271 also describes the overall
standards and requirements for
authorization.
After a state receives initial
authorization, new regulatory
requirements promulgated under the
authority in the RCRA statute which
existed prior to the 1984 Hazardous and
Solid Waste Amendments (HSWA) do
not apply in that state until the state
adopts equivalent state requirements.
The state must adopt such requirements
to maintain authorization.
In contrast, under RCRA section
3006(g) (i.e., 42 U.S.C. 6926(g)), new
Federal requirements and prohibitions
imposed pursuant to HSWA provisions
take effect in authorized states at the
same time that they take effect in
unauthorized states. Although
authorized states are still required to
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update their hazardous waste programs
to remain equivalent to the Federal
program, EPA carries out HSWA
requirements and prohibitions in
authorized states, including the
issuance of new permits implementing
those requirements, until EPA
authorizes the state to do so.
Finally, authorized states are required
to modify their programs only when
EPA promulgates Federal requirements
that are more stringent or broader in
scope than existing Federal
requirements. RCRA section 3009
allows the states to impose standards
more stringent than those in the Federal
program. See also § 271.1(i). Therefore,
authorized states are not required to
adopt Federal regulations, both HSWA
and non-HSWA, that are considered less
stringent.
B. Authorization of States for Today’s
Rule
Today’s rule affects many aspects of
the RCRA Program and is promulgated
pursuant to both HSWA and non-HSWA
statutory authority. Therefore, the
Agency added the rule to Table 1 in
§ 271.1(j), which identifies Federal
regulations that are promulgated
pursuant to the statutory authority that
was added by HSWA. States may apply
for final authorization for the HSWA
provisions, as discussed in the
following section of this preamble.
Today’s rule language provides
standards that are equivalent to or less
stringent than the existing provisions in
the Federal regulations which they
would amend. Therefore, States would
not be required to adopt and seek
authorization for this rulemaking. EPA
would implement this rulemaking only
in those states which are not authorized
for the RCRA Program, and will
implement provisions promulgated
pursuant to HSWA only in those states
which have not received authorization
for the HSWA provision that would be
amended. In authorized States, the
changes will not be applicable until and
unless the State revises its program to
adopt the revisions.
(Note: Procedures and deadlines for
State program revisions are set forth in
§ 271.21.)
This rule will provide significant
benefits to EPA, the states, and the
regulated community, without
compromising human health or
environmental protection. Therefore,
EPA strongly encourages authorized
states to amend their programs and seek
authorization for today’s rule.
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C. Abbreviated Authorization
Procedures
EPA consider’s today’s rule to be a
minor rulemaking and is adding it to the
list of minor or routine rulemakings in
Table 1 to § 271.21. Placement in this
table will enable states to use the
abbreviated procedures located in
§ 271.21(h) when they seek
authorization for today’s changes. These
abbreviated procedures were established
in the HWIR-media rulemaking (see 63
FR 65927, November 30, 1998).
XIII. Statutory and Executive Order
Reviews
A. Executive Order 12866: Regulatory
Planning and Review
Under Executive Order 12866 (58 FR
51735, October 4, 1993), we must
determine whether a regulatory action is
‘‘significant,’’ and therefore subject to
Office of Management and Budget
(OMB) review and the requirements of
the Executive Order. The order defines
a ‘‘significant regulatory action’’ as one
that is likely to result in a rule that may:
(1) Have an annual effect on the
economy of $100 million or more,
adversely affect in a material way the
economy, a sector of the economy,
productivity, competition, jobs, the
environment, public health or safety, or
State, local, or tribal governments or
communities;
(2) Create a serious inconsistency or
otherwise interfere with an action taken
or planned by another agency;
(3) Materially alter the budgetary
impact of entitlements, grants, user fees,
or loan programs or the rights and
obligations of recipients thereof; or
(4) Raise novel legal or policy issues
arising out of legal mandates, the
President’s priorities, or the principles
set forth in this Executive Order.
OMB determined that this rule is not
a ‘‘significant regulatory action’’ under
the terms of Executive Order 12866 and
is therefore not subject to OMB review
and the requirements of the Executive
Order.
B. Paperwork Reduction Act
This action does not impose any new
information collection burden. There
are no additional reporting, notification,
or recordkeeping provisions associated
with today’s rule. However, the Office of
Management and Budget (OMB)
previously approved the information
collection requirements contained in
some of the existing regulations being
revised by this rule, under the
provisions of the Paperwork Reduction
Act, 44 U.S.C. 3501 et seq., and assigned
OMB control numbers for those
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information collection requirements, as
follows:
—40 CFR 258.28: OMB control number
2050–0122
—40 CFR 260.21 and 260.22: OMB
control number 2050–0053
—40 CFR 261.3: OMB control number
2050–0085
—40 CFR 261.35: OMB control number
2050—0115
—40 CFR 264.1034, 264.1063, 265.1034,
and 265.1063: OMB control number
2050–0050
—40 CFR 266.100, 266.102, 266.106,
266.112, Appendix IX to part 63, and
270.22: OMB control number 2050–
0073
—40 CFR 270.19: OMB control number
2050–0009
—40 CFR 270.62: OMB control numbers
2050–0009 and 2050–0149
—40 CFR 270.66: OMB control numbers
2050–0073 and 2050–0149
—40 CFR 279.10, 279.44, 279.53 and
279.63: OMB control number 2050–
0124
Copies of the ICR document(s) may be
obtained from Sandy Farmer, by mail at
the Office of Environmental
Information, Collection Strategies
Division; U.S. Environmental Protection
Agency (2822); 1200 Pennsylvania Ave.,
NW., Washington, DC 20460, by email
at farmer.sandy@epa.gov, or by calling
(202) 260–2740. A copy may also be
downloaded off the Internet at https://
www.epa.gov/icr. Include the ICR and/
or OMB number in any correspondence.
Burden means the total time, effort, or
financial resources expended by persons
to generate, maintain, retain, or disclose
or provide information to or for a
Federal agency. This includes the time
needed to review instructions; develop,
acquire, install, and utilize technology
and systems for the purposes of
collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information; adjust the
existing ways to comply with any
previously applicable instructions and
requirements; train personnel to be able
to respond to a collection of
information; search data sources;
complete and review the collection of
information; and transmit or otherwise
disclose the information.
An Agency may not conduct or
sponsor, and a person is not required to
respond to a collection of information,
unless it displays a currently valid OMB
control number. The OMB control
numbers for EPA’s regulations are listed
in 40 CFR part 9 and 48 CFR chapter 15.
C. Regulatory Flexibility Act
The Regulatory Flexibility Act
generally requires an agency to prepare
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a regulatory flexibility analysis of any
rule subject to notice and comment
rulemaking requirements under the
Administrative Procedure Act or any
other statute, unless the agency certifies
that the rule will not have a significant
economic impact on a substantial
number of small entities. Small entities
include small businesses, small
organizations, and small governmental
jurisdictions.
For purposes of assessing the impacts
of today’s rule on small entities, small
entity is defined as: (1) A small business
that is independently owned and
operated and not dominant in its field
as defined by Small Business
Administration (SBA) regulations under
Section 3 of the Small Business Act for
SIC; (2) a small governmental
jurisdiction that is a government of a
city, county, town, school district or
special district with a population of less
than 50,000; and (3) a small
organization that is any not-for-profit
enterprise which is independently
owned and operated and is not
dominant in its field.
After considering the economic
impacts of today’s final rule on small
entities, I certify that this action will not
have a significant economic impact on
a substantial number of small entities.
In determining whether a rule has a
significant economic impact on a
substantial number of small entities, the
impact of concern is any significant
adverse economic impact on small
entities, since the primary purpose of
the regulatory flexibility analyses is to
identify and address regulatory
alternatives ‘‘which minimize any
significant economic impact of the rule
on small entities.’’ 5 U.S.C. sections 603
and 604. Thus, an agency may certify
that a rule will not have a significant
economic impact on a substantial
number of small entities if the rule
relieves regulatory burden, or otherwise
has a positive economic effect on all of
the small entities subject to the rule.
Today’s rule is specifically intended to
reduce economic burden for all entities.
The action will provide greater
flexibility and utility to all affected
entities, including small entities, by
providing an increase in choices of
appropriate analytical methods for
RCRA applications. It does not create
any new regulatory requirements or
require any new reports beyond those
now required by the revised regulations.
In addition, its revisions need not be
adopted by regulated entities. If the
methods are appropriate, such entities
can continue to use the methods
previously specified in the regulations
before today instead of choosing the
option to use other appropriate methods
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from other reliable sources. We have
therefore concluded that today’s final
rule will relieve regulatory burden for
small entities.
D. Unfunded Mandates Reform Act
Title II of the Unfunded Mandates
Reform Act of 1995 (UMRA or the Act),
Pubic Law 104–4, establishes
requirements for Federal agencies to
assess the effects of their regulatory
actions on State, local, and tribal
governments and the private sector.
Under section 202 of UMRA, EPA
generally must prepare a written
statement, including a cost-benefit
analysis, for proposed rules and final
rules with Federal mandates that may
result in estimated costs to State, local,
and tribal governments in the aggregate,
or to the private sector, of $100 million
or more in any one year. When such a
statement is needed, section 205 of the
Act generally requires EPA to identify
and consider a reasonable number of
regulatory alternatives. Under section
205, EPA must adopt the least costly,
most cost-effective or least burdensome
alternative that achieves the objectives
of the rule, unless the Administrator
explains in the final rule why that
alternative was not adopted. The
provisions of section 205 do not apply
when they are inconsistent with
applicable law. Before EPA establishes
regulatory requirements that may
significantly or uniquely affect small
governments, including tribal
governments, it must develop under
section 203 of the Act a small
government agency plan. The plan must
provide for notifying potentially
affected small governments, giving them
meaningful and timely input in the
development of EPA regulatory
proposals with significant Federal
intergovernmental mandates, and
informing, educating, and advising them
on compliance with the regulatory
requirements.
First, this rule does not contain a
Federal mandate. The rule imposes no
enforceable duty on any State, local or
tribal governments. This rule contains
no regulatory requirements that might
significantly or uniquely affect small
governments. This is due to the fact that
this rule does not add any new
regulatory requirements and States need
not adopt its revisions. This rule only
revises certain regulatory sections to
remove the requirement to use SW–846
methods and allow the use of other
appropriate methods—that is, clarify
allowed flexibility in method selection
for meeting RCRA-related testing and
monitoring requirements. Under RCRA,
regardless of the method used—the one
previously specified in the regulation
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34553
before today or another appropriate
method—regulated entities should be
demonstrating that the method is
appropriate for its intended use. This
rule also does not propose new
monitoring or information collection
requirements. The additional flexibility
allowed by this rule should result in
improved data quality at reduced cost.
Thus, today’s rule is not subject to the
requirements of sections 202, 203 and
205 of UMRA.
E. Executive Order 13132: Federalism
Executive Order 13132, entitled
‘‘Federalism’’ (64 FR 43255, August 10,
1999), requires EPA to develop an
accountable process to ensure
‘‘meaningful and timely input by State
and local officials in the development of
regulatory policies that have federalism
implications.’’ ‘‘Policies that have
federalism implications’’ is defined in
the Executive Order to include
regulations that have ‘‘substantial direct
effects on the States, on the relationship
between the National Government and
the States, or on the distribution of
power and responsibilities among the
various levels of government.’’
This final rule does not have
federalism implications. It will not have
substantial direct effects on the States,
on the relationship between the
National Government and the States, or
on the distribution of power and
responsibilities among the various
levels of government, as specified in
Executive Order 13132. As explained
above, today’s rule does not impose new
requirements on the States and its
regulatory changes need not be adopted
by the States. Thus, Executive Order
13132 does not apply to this rule.
Because these changes are equivalent to
or less stringent than the existing
Federal program, States would not be
required to adopt and seek authorization
for them.
F. Executive Order 13175: Consultation
and Coordination With Indian Tribal
Governments
Executive Order 13175 (65 FR 67249)
entitled, ‘‘Consultation and
Coordination With Indian Tribal
Governments’’ requires EPA to develop
an accountable process to ensure
‘‘meaningful and timely input by tribal
officials in the development of
regulatory policies that have tribal
implications. ‘‘Policies that have tribal
implications’’ are defined in the
Executive Order to include regulations
that have ‘‘substantial direct effects on
one or more Indian tribes, or on the
distribution of power and
responsibilities between the Federal
Government and Indian tribes.’’
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Today’s rule does not have tribal
implications. It will not have substantial
direct effects on tribal governments, on
the relationship between the Federal
Government and Indian tribes, or on the
distribution of power and
responsibilities between the Federal
Government and Indian tribes, as
specified in Executive Order 13175. For
many of the same reasons described
above under unfunded mandates, the
requirements of the Executive Order do
not apply to this rulemaking. As stated
above, this rule does not propose any
new regulatory requirements and Indian
tribal governments need not adopt it. It
does not impose any direct compliance
costs on tribal governments.
G. Executive Order 13045: Protection of
Children From Environmental Health
Risks and Safety Risks
Executive Order 13045, ‘‘Protection of
Children From Environmental Health
Risks and Safety Risks’’ (62 FR 19885,
April 23, 1997) applies to any rule that:
(1) Is determined to be ‘‘economically
significant’’ as defined under Executive
Order 12866, and (2) concerns an
environmental health or safety risk that
EPA has reason to believe may have a
disproportionate effect on children. If
the regulatory action meets both criteria,
the Agency must evaluate the
environmental health or safety effects of
the planned rule on children, and
explain why the planned regulation is
preferable to other potentially effective
and reasonably feasible alternatives
considered by the Agency.
This rule is not subject to the
Executive Order because it is not
economically significant as defined in
Executive Order 12866. Also, EPA
interprets Executive Order 13045 as
applying only to those regulatory
actions that are based on health or safety
risks, such that the analysis required
under section 5–501 of the Order has
the potential to influence the regulation.
This rule is not subject to Executive
Order 13045 because it does not
establish an environmental standard
intended to mitigate health or safety
risks. The action discussed in today’s
rule is intended to provide increased
flexibility in the use of methods for
RCRA-related testing and monitoring,
and thus is not subject to Executive
Order 13045.
H. Executive Order 13211: Actions That
Significantly Affect Energy Supply,
Distribution, or Use
This rule is not a ‘‘significant energy
action’’ as defined in Executive Order
13211, ‘‘Actions Concerning Regulations
that Significantly Affect Energy Supply,
Distribution, or Use’’ (66 FR 28355, May
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22, 2001) because it is not likely to have
a significant adverse effect on the
supply, distribution, or use of energy.
Further, we have concluded that this
rule is not likely to have any adverse
energy effects.
I. National Technology Transfer and
Advancement Act
Section 12(d) of the National
Technology Transfer and Advancement
Act of 1995 (‘‘NTTAA’’), Public Law No.
104–113, section 12(d) (15 U.S.C. 272
note) directs EPA to use voluntary
consensus standards in its regulatory
activities unless to do so would be
inconsistent with applicable law or
otherwise impractical. Voluntary
consensus standards are technical
standards (e.g., materials specifications,
test methods, sampling procedures, and
business practices) that are developed or
adopted by voluntary consensus
standards bodies. The NTTAA directs
us to provide Congress, through OMB,
explanations when the Agency decides
not to use available and applicable
voluntary consensus standards.
This rule increases flexibility in the
use of methods for RCRA-related testing
and monitoring and does not itself
identify or require the use of new
methods or other technical standards. In
fact, this rule, may increase the use of
available voluntary consensus standards
for some RCRA applications, provided
that such methods are appropriate for
the regulatory application.
J. Executive Order 12898: Federal
Actions To Address Environmental
Justice in Minority Populations and
Low-Income Populations
Executive Order 12898, ‘‘Federal
Actions to Address Environmental
Justice in Minority Populations and
Low-Income Populations,’’ February 11,
1994, requires that regulatory actions be
accompanied by an environmental
justice analysis. This analysis must look
at potentially disproportionate impacts
the action may have on minority and/or
low-income communities.
The Agency has determined that the
action does not raise environmental
justice concerns. The impact of this rule
will be to provide increased flexibility
in the choice of appropriate analytical
methods for RCRA applications. The
Agency is not aware of any
disproportionate impacts that such
flexibility may have on minority and/or
low-income communities.
K. Congressional Review Act
The Congressional Review Act, 5
U.S.C. 801 et seq., as added by the Small
Business Regulatory Enforcement
Fairness Act of 1996, generally provides
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Sfmt 4700
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report, which includes a
copy of the rule, to each House of the
Congress and to the Comptroller General
of the United States. EPA will submit a
report containing this rule and other
required information to the U.S. Senate,
the U.S. House of Representatives, and
the Comptroller General of the United
States prior to publication of the rule in
the Federal Register. A major rule
cannot take effect until 60 days after it
is published in the Federal Register.
This action is not a ‘‘major rule’’ as
defined by 5 U.S.C. 804(2). This rule
will be effective July 14, 2005.
List of Subjects
40 CFR Part 63
Environmental protection, Air
pollution control, Hazardous
substances, Reporting and
recordkeeping requirements.
40 CFR Part 258
Environmental protection,
Incorporation by reference, Reporting
and recordkeeping requirements, Waste
treatment and disposal, Water pollution
control.
40 CFR Part 260
Environmental protection,
Administrative practice and procedure,
Confidential business information,
Hazardous waste, Incorporation by
reference, Reporting and recordkeeping
requirements.
40 CFR Part 261
Environmental protection,
Comparable fuels, syngas fuels,
Excluded hazardous waste,
Incorporation by reference, Reporting
and recordkeeping requirements.
40 CFR Part 264
Environmental protection, Air
pollution control, Hazardous waste,
Incorporation by reference, Insurance,
Packaging and containers, Reporting
and recordkeeping requirements,
Security measures, Surety bonds.
40 CFR Part 265
Environmental protection, Air
pollution control, Hazardous waste,
Incorporation by reference, Insurance,
Packaging and containers, Reporting
and recordkeeping requirements,
Security measures, Surety bonds, Water
supply.
40 CFR Part 266
Environmental protection, Energy,
Hazardous waste, Incorporation by
reference, Recycling, Reporting and
recordkeeping requirements.
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Federal Register / Vol. 70, No. 113 / Tuesday, June 14, 2005 / Rules and Regulations
40 CFR Part 268
PART 63—NATIONAL EMISSION
STANDARDS FOR HAZARDOUS AIR
POLLUTANTS FOR SOURCE
CATEGORIES
§ 258.28
34555
Liquids restrictions.
40 CFR Part 270
Authority: 33 U.S.C. 1345(d) and (e); 42
U.S.C 6902(a), 6907, 6912(a), 6944, 6945(c),
and 6949a(c).
*
*
*
*
(c) * * *
(1) Liquid waste means any waste
material that is determined to contain
‘‘free liquids’’ as defined by Method
9095B (Paint Filter Liquids Test),
included in ‘‘Test Methods for
Evaluating Solid Waste, Physical/
Chemical Methods’’ (EPA Publication
SW–846) which is incorporated by
reference. A suffix of ‘‘B’’ in the method
number indicates revision two (the
method has been revised twice). Method
9095B is dated November 2004. This
incorporation by reference was
approved by the Director of the Federal
Register pursuant to 5 U.S.C. 552(a) and
1 CFR part 51. This material is
incorporated as it exists on the date of
approval and a notice of any change in
this material will be published in the
Federal Register. A copy may be
inspected at the Library, U.S.
Environmental Protection Agency, 1200
Pennsylvania Ave., NW. (3403T),
Washington, DC 20460,
libraryhq@epa.gov; or at the National
Archives and Records Administration
(NARA). For information on the
availability of this material at NARA,
call 202–741–6030, or go to: https://
www.archives.gov/federal_register/
code_of_federal_regulations/
ibr_locations.html.
*
*
*
*
*
Subpart C—Operating Criteria
I
4. Section 258.28 is amended by
revising paragraph (c)(1) to read as
follows:
Environmental protection, Hazardous
waste, Incorporation by reference,
Reporting and recordkeeping
requirements.
Appendix I to Part 258—Constituents
for Detection Monitoring
1. The authority citation for part 63
continues to read as follows:
I
Authority: 42 U.S.C. 7401 et seq.
Environmental protection,
Administrative practice and procedure,
Confidential business information,
Hazardous materials transportation,
Hazardous waste, Reporting and
recordkeeping requirements, Water
pollution control, Water supply.
40 CFR Part 271
Subpart EEE—National Emission
Standards for Hazardous Air Pollutants
From Hazardous Waste Combustors
2. Section 63.1208 is amended by
revising paragraph (b)(8) to read as
follows:
I
§ 63.1208
Environmental protection,
Administrative practice and procedure,
Confidential business information,
Hazardous materials transportation,
Hazardous waste, Indians-lands,
Intergovernmental relations, Penalties,
Reporting and recordkeeping
requirements, Water pollution control,
Water supply.
40 CFR Part 279
Environmental protection, Petroleum,
Recycling, Reporting and recordkeeping
requirements.
What are the test methods?
*
*
*
*
*
(b) * * *
(8) Feedstream analytical methods.
You may use any reliable analytical
method to determine feedstream
concentrations of metals, chlorine, and
other constituents. It is your
responsibility to ensure that the
sampling and analysis procedures are
unbiased, precise, and that the results
are representative of the feedstream.
*
*
*
*
*
PART 258—CRITERIA FOR MUNICIPAL
SOLID WASTE LANDFILLS
3. The authority citation for part 258
continues to read as follows:
I
Dated: May 16, 2005.
Stephen L. Johnson,
Administrator.
For the reasons set out in the preamble,
EPA amends title 40, chapter I, of the
Code of Federal Regulations as follows:
I
I
*
5. Appendix I to part 258 is revised to
read as follows:
Common name 1
CAS RN 2
Inorganic Constituents:
(1) Antimony ...................................................................................................................................................................................
(2) Arsenic ......................................................................................................................................................................................
(3) Barium ......................................................................................................................................................................................
(4) Beryllium ...................................................................................................................................................................................
(5) Cadmium ..................................................................................................................................................................................
(6) Chromium .................................................................................................................................................................................
(7) Cobalt .......................................................................................................................................................................................
(8) Copper ......................................................................................................................................................................................
(9) Lead ..........................................................................................................................................................................................
(10) Nickel ......................................................................................................................................................................................
(11) Selenium .................................................................................................................................................................................
(12) Silver .......................................................................................................................................................................................
(13) Thallium ..................................................................................................................................................................................
(14) Vanadium ...............................................................................................................................................................................
(15) Zinc .........................................................................................................................................................................................
Organic Constituents:
(16) Acetone ..................................................................................................................................................................................
(17) Acrylonitrile 1 ..........................................................................................................................................................................
(18) Benzene .................................................................................................................................................................................
(19) Bromochloromethane .............................................................................................................................................................
(20) Bromodichloromethane ..........................................................................................................................................................
(21) Bromoform; Tribromomethane ...............................................................................................................................................
(22) Carbon disulfide .....................................................................................................................................................................
(23) Carbon tetrachloride ...............................................................................................................................................................
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(Total)
(Total)
(Total)
(Total)
(Total)
(Total)
(Total)
(Total)
(Total)
(Total)
(Total)
(Total)
(Total)
(Total)
(Total)
67–64–1
107–13–1
71–43–2
74–97–5
75–27–4
75–25–2
75–15–0
56–23–5
34556
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Common name 1
(24)
(25)
(26)
(27)
(28)
(29)
(30)
(31)
(32)
(33)
(34)
(35)
(36)
(37)
(38)
(39)
(40)
(41)
(42)
(43)
(44)
(45)
(46)
(47)
(48)
(49)
(50)
(51)
(52)
(53)
(54)
(55)
(56)
(57)
(58)
(59)
(60)
(61)
(62)
CAS RN 2
Chlorobenzene .......................................................................................................................................................................
Chloroethane; Ethyl chloride ..................................................................................................................................................
Chloroform; Trichloromethane ................................................................................................................................................
Dibromochloromethane; Chlorodibromomethane ..................................................................................................................
1,2-Dibromo-3-chloropropane; DBCP ....................................................................................................................................
1,2-Dibromoethane; Ethylene dibromide; EDB ......................................................................................................................
o-Dichlorobenzene; 1,2-Dichlorobenzene ..............................................................................................................................
p-Dichlorobenzene; 1,4-Dichlorobenzene ..............................................................................................................................
trans-1, 4-Dichloro-2-butene ..................................................................................................................................................
1,1-Dichlorethane; Ethylidene chloride ..................................................................................................................................
1,2-Dichlorethane; Ethylene dichloride ..................................................................................................................................
1,1-Dichloroethylene; 1,1-Dichloroethene; Vinylidene chloride .............................................................................................
cis-1,2-Dichloroethylene; cis-1,2-Dichloroethene ...................................................................................................................
trans-1, 2-Dichloroethylene; trans-1,2-Dichloroethene ..........................................................................................................
1,2-Dichloropropane; Propylene dichloride ............................................................................................................................
cis-1,3-Dichloropropene .........................................................................................................................................................
trans-1,3-Dichloropropene ......................................................................................................................................................
Ethylbenzene ..........................................................................................................................................................................
2-Hexanone; Methyl butyl ketone ..........................................................................................................................................
Methyl bromide; Bromomethane ............................................................................................................................................
Methyl chloride; Chloromethane ............................................................................................................................................
Methylene bromide; Dibromomethane ...................................................................................................................................
Methylene chloride; Dichloromethane ....................................................................................................................................
Methyl ethyl ketone; MEK; 2-Butanone .................................................................................................................................
Methyl iodide; Idomethane .....................................................................................................................................................
4-Methyl-2-pentanone; Methyl isobutyl ketone ......................................................................................................................
Styrene ...................................................................................................................................................................................
1,1,1,2-Tetrachloroethane ......................................................................................................................................................
1,1,2,2-Tetrachloroethane ......................................................................................................................................................
Tetrachloroethylene; Tetrachloroethene; Perchloroethylene .................................................................................................
Toluene ...................................................................................................................................................................................
1,1,1-Trichloroethane; Methylchloroform ................................................................................................................................
1,1,2-Trichloroethane .............................................................................................................................................................
Trichloroethylene; Trichloroethene .........................................................................................................................................
Trichlorofluoromethane; CFC–11 ...........................................................................................................................................
1,2,3-Trichloropropane ...........................................................................................................................................................
Vinyl acetate ...........................................................................................................................................................................
Vinyl chloride ..........................................................................................................................................................................
Xylenes ...................................................................................................................................................................................
108–90–7
75–00–3
67–66–3
124–48–1
96–12–8
106–93–4
95–50–1
106–46–7
110–57–6
75–34–3
107–06–2
75–35–4
156–59–2
156–60–5
78–87–5
10061–01–5
10061–02–6
100–41–4
591–78–6
74–83–9
74–87–3
74–95–3
75–09–2
78–93–3
74–88–4
108–10–1
100–42–5
630–20–6
79–34–5
127–18–4
108–88–3
71–55–6
79–00–5
79–01–6
75–69–4
96–18–4
108–05–4
75–01–4
1330–20–7
1 Common names are those widely used in government regulations, scientific publications, and commerce; synonyms exist for many chemicals.
2 Chemical Abstract Service registry number. Where ‘‘Total’’ is entered, all species in the ground water that contain this element are included.
6. Appendix II to part 258 is revised to
read as follows:
I
Appendix II to Part 258—List of
Hazardous Inorganic and Organic
Constituents
Common name 1
CAS RN 2
Chemical abstracts service index name 3
Acenaphthene ............................................................................
Acenaphthylene .........................................................................
Acetone ......................................................................................
Acetonitrile; Methyl cyanide .......................................................
Acetophenone ............................................................................
2-Acetylaminofluorene; 2-AAF ...................................................
Acrolein ......................................................................................
Acrylonitrile ................................................................................
Aldrin ..........................................................................................
83–32–9 ...........
208–96–8 .........
67–64–1 ...........
75–05–8 ...........
98–86–2 ...........
53–96–3 ...........
107–02–8 .........
107–13–1 .........
309–00–2 .........
Allyl chloride ...............................................................................
4-Aminobiphenyl ........................................................................
Anthracene .................................................................................
Antimony ....................................................................................
Arsenic .......................................................................................
Barium ........................................................................................
Benzene .....................................................................................
Benzo[a]anthracene; Benzanthracene ......................................
Benzo[b]fluoranthene .................................................................
Benzo[k]fluoranthene .................................................................
Benzo[ghi]perylene ....................................................................
Benzo[a]pyrene ..........................................................................
Benzyl alcohol ............................................................................
107–05–1 .........
92–67–1 ...........
120–12–7 .........
(Total) ...............
(Total) ...............
(Total) ...............
71–43–2 ...........
56–55–3 ...........
205–99–2 .........
207–08–9 .........
191–24–2 .........
50–32–8 ...........
100–51–6 .........
Acenaphthylene, 1,2-dihydroAcenaphthylene
2-Propanone
Acetonitrile
Ethanone, 1-phenylAcetamide, N–9H-fluoren-2-yl2-Propenal
2-Propenenitrile
1,4:5,8-Dimethanonaphthalene,
1,2,3,4,10,10-hexachloro1,4,4a,5,8,8a-hexahydro-(1,4,4a,5,8,8a)1-Propene, 3-chloro[1,1′-Biphenyl]- 4-amine
Anthracene
Antimony
Arsenic
Barium
Benzene
Benz[a]anthracene
Benz[e]acephenanthrylene
Benzo[k]fluoranthene
Benzo[ghi]perylene
Benzo[a]pyrene
Benzenemethanol
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Common name 1
CAS RN 2
Chemical abstracts service index name 3
Beryllium ....................................................................................
alpha-BHC .................................................................................
beta-BHC ...................................................................................
delta-BHC ..................................................................................
gamma-BHC; Lindane ...............................................................
Bis(2-chloroethoxy)methane ......................................................
Bis(2-chloroethyl)ether; Dichloroethyl ether ..............................
Bis(2-chloro-1-methylethyl)
ether;
2,2′-Dichlorodiisopropyl
ether; DCIP, See footnote 4.
Bis(2-ethylhexyl) phthalate ........................................................
Bromochloromethane; Chlorobromethane .................................
Bromodichloromethane; Dibromochloromethane ......................
Bromoform; Tribromomethane ...................................................
4-Bromophenyl phenyl ether .....................................................
Butyl benzyl phthalate; Benzyl butyl phthalate ..........................
Cadmium ....................................................................................
Carbon disulfide .........................................................................
Carbon tetrachloride ..................................................................
Chlordane ..................................................................................
(Total) ...............
319–84–6 .........
319–85–7 .........
319–86–8 .........
58–89–9 ...........
111–91–1 .........
111–44–4 .........
108–60–1 .........
Beryllium
Cyclohexane, 1,2,3,4,5,6-hexachloro-,(1a,2a,3b,4a,5b,6b)Cyclohexane, 1,2,3,4,5,6-hexachloro-,(1a,2b,3a,4b,5a,6b)Cyclohexane, 1,2,3,4,5,6-hexachloro-,(1a,2a,3a,4b,5a,6b)Cyclohexane, 1,2,3,4,5,6- hexachloro-,(1a,2a, 3b, 4a,5a,6b)Ethane, 1,1′-[methylenebis (oxy)]bis [2-chloroEthane, 1,1′-oxybis[2-chloroPropane, 2,2′-oxybis[1-chloro-
117–81–7 .........
74–97–5 ...........
75–27–4 ...........
75–25–2 ...........
101–55–3 .........
85–68–7 ...........
(Total) ...............
75–15–0 ...........
56–23–5 ...........
See footnote 5 ..
p-Chloroaniline ...........................................................................
Chlorobenzene ...........................................................................
Chlorobenzilate ..........................................................................
106–47–8 .........
108–90–7 .........
510–15–6 .........
p-Chloro-m-cresol; 4-Chloro-3-methylphenol .............................
Chloroethane; Ethyl chloride .....................................................
Chloroform; Trichloromethane ...................................................
2-Chloronaphthalene .................................................................
2-Chlorophenol ..........................................................................
4-Chlorophenyl phenyl ether .....................................................
Chloroprene ...............................................................................
Chromium ..................................................................................
Chrysene ....................................................................................
Cobalt .........................................................................................
Copper .......................................................................................
m-Cresol; 3-Methylphenol ..........................................................
o-Cresol; 2-Methylphenol ...........................................................
p-Cresol; 4-Methylphenol ...........................................................
Cyanide ......................................................................................
2,4-D; 2,4-Dichlorophenoxyacetic acid ......................................
4,4′-DDD ....................................................................................
4,4′-DDE ....................................................................................
4,4′-DDT .....................................................................................
Diallate .......................................................................................
59–50–7 ...........
75–00–3 ...........
67–66–3 ...........
91–58–7 ...........
95–57–8 ...........
7005–72–3 .......
126–99–8 .........
(Total) ...............
218–01–9 .........
(Total) ...............
(Total) ...............
108–39–4 .........
95–48–7 ...........
106–44–5 .........
57–12–5 ...........
94–75–7 ...........
72–54–8 ...........
72–55–9 ...........
50–29–3 ...........
2303–16–4 .......
Dibenz[a,h]anthracene ...............................................................
Dibenzofuran ..............................................................................
Dibromochloromethane; Chlorodibromomethane ......................
1,2-Dibromo-3-chloropropane; DBCP ........................................
1,2-Dibromoethane; Ethylene dibromide; EDB .........................
Di-n-butyl phthalate ....................................................................
o-Dichlorobenzene; 1,2-Dichlorobenzene .................................
m-Dichlorobenzene; 1,3-Dichlorobenzene ................................
p-Dichlorobenzene; 1,4-Dichlorobenzene .................................
3,3′-Dichlorobenzidine ...............................................................
trans-1,4-Dichloro-2-butene .......................................................
Dichlorodifluoromethane; CFC 12 .............................................
1,1-Dichloroethane; Ethyldidene chloride ..................................
1,2-Dichloroethane; Ethylene dichloride ....................................
1,1-Dichloroethylene; 1,1-Dichloroethene;
Vinylidene
chloride
cis-1,2-Dichloroethylene;
cis-1,2Dichloroethene.
trans-1,2-Dichloroethylene; trans-1,2-Dichloroethene ...............
2,4-Dichlorophenol .....................................................................
2,6-Dichlorophenol .....................................................................
1,2-Dichloropropane ..................................................................
1,3-Dichloropropane; Trimethylene dichloride ...........................
2,2-Dichloropropane; Isopropylidene chloride ...........................
1,1-Dichloropropene ..................................................................
cis-1,3-Dichloropropene .............................................................
trans-1,3-Dichloropropene .........................................................
Dieldrin .......................................................................................
53–70–3 ...........
132–64–9 .........
124–48–1 .........
96–12–8 ...........
106–93–4 .........
84–74–2 ...........
95–50–1 ...........
541–73–1 .........
106–46–7 .........
91–94–1 ...........
110–57–6 .........
75–71–8 ...........
75–34–3 ...........
107–06–2 .........
75–35–4 ...........
156–59–2 .........
1,2-Benzenedicarboxylic acid, bis(2-ethylhexyl)ester
Methane, bromochloroMethane, bromodichloroMethane, tribromoBenzene, 1-bromo-4-phenoxy1,2-Benzenedicarboxylic acid, butyl phenylmethyl ester
Cadmium
Carbon disulfide
Methane, tetrachloro4,7-Methano-1H-indene,
1,2,4,5,6,7,8,8-octachloro2,3,3a,4,7,7a-hexahydroBenzenamine, 4-chloroBenzene, chloroBenzeneacetic acid, 4-chloro-(4-chlorophenyl)-hydroxy-, ethyl ester.
Phenol, 4-chloro-3-methylEthane, chloroMethane, trichloroNaphthalene, 2-chloroPhenol, 2-chloroBenzene, 1-chloro-4-phenoxy1,3-Butadiene, 2-chloroChromium
Chrysene
Cobalt
Copper
Phenol, 3-methylPhenol, 2-methylPhenol, 4-methylCyanide
Acetic acid, (2,4-dichlorophenoxy)Benzene 1,1′-(2,2-dichloroethylidene) bis[4-chloroBenzene, 1,1′-(dichloroethenylidene) bis[4-chloroBenzene, 1,1′-(2,2,2-trichloroethylidene) bis[4-chloroCarbamothioic acid, bis(1-methylethyl)-, S- (2,3-dichloro-2propenyl) ester.
Dibenz[a,h]anthracene
Dibenzofuran
Methane, dibromochloroPropane, 1,2-dibromo-3-chloroEthane, 1,2-dibromo1,2-Benzenedicarboxylic acid, dibutyl ester
Benzene, 1,2-dichloroBenzene, 1,3-dichloroBenzene, 1,4-dichloro[1,1′-Biphenyl]-4,4′-diamine, 3,3′-dichloro2-Butene, 1,4-dichloro-, (E)Methane, dichlorodifluoroEthane, 1,1-dichloroEthane, 1,2-dichloroEthene, 1,1-dichloroEthene, 1,2-dichloro-(Z)-
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156–60–5 .........
120–83–2 .........
87–65–0 ...........
78–87–5 ...........
142–28–9 .........
594–20–7 .........
563–58–6 .........
10061–01–5 .....
10061–02–6 .....
60–57–1 ...........
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Ethene, 1,2-dichloro-, (E)Phenol, 2,4-dichloroPhenol, 2,6-dichloroPropane, 1,2-dichloroPropane, 1,3-dichloroPropane, 2,2-dichloro1-Propene, 1,1-dichloro1-Propene, 1,3-dichloro-, (Z)1-Propene, 1,3-dichloro-, (E)2,7:3,6-Dimethanonaphth
[2,3-b]oxirene,
hexachloro-1a,2,2a,3,6,6a,7,7a-octahydro-,
2aa,3b,6b,6aa,7b,7aa)E:\FR\FM\14JNR2.SGM
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Common name 1
CAS RN 2
Chemical abstracts service index name 3
Diethyl phthalate ........................................................................
O,O-Diethyl O–2-pyrazinyl phosphorothioate; Thionazin ..........
Dimethoate .................................................................................
84–66–2 ...........
297–97–2 .........
60–51–5 ...........
p-(Dimethylamino)azobenzene ..................................................
7,12-Dimethylbenz[a]anthracene ...............................................
3,3′-Dimethylbenzidine ...............................................................
alpha, &alpha-Dimethylphenethylamine ....................................
2,4-Dimethylphenol; m-Xylenol ..................................................
Dimethyl phthalate .....................................................................
m-Dinitrobenzene .......................................................................
4,6-Dinitro-o-cresol; 4,6-Dinitro-2-methylphenol ........................
2,4-Dinitrophenol ........................................................................
2,4-Dinitrotoluene .......................................................................
2,6-Dinitrotoluene .......................................................................
Dinoseb; DNBP; 2-sec-Butyl-4,6-dinitrophenol .........................
Di-n-octyl phthalate ....................................................................
Diphenylamine ...........................................................................
Disulfoton ...................................................................................
60–11–7 ...........
57–97–6 ...........
119–93–7 .........
122–09–8 .........
105–67–9 .........
131–11–3 .........
99–65–0 ...........
534–52–1 .........
51–28–5 ...........
121–14–2 .........
606–20–2 .........
88–85–7 ...........
117–84–0 .........
122–39–4 .........
298–04–4 .........
Endosulfan I ...............................................................................
959–98–8 .........
Endosulfan II ..............................................................................
33213–65–9 .....
Endosulfan sulfate .....................................................................
1031–07–8 .......
Endrin .........................................................................................
72–20–8 ...........
Endrin aldehyde .........................................................................
7421–93–4 .......
Ethylbenzene .............................................................................
Ethyl methacrylate .....................................................................
Ethyl methanesulfonate .............................................................
Famphur .....................................................................................
100–41–4 .........
97–63–2 ...........
62–50–0 ...........
52–85–7 ...........
Fluoranthene ..............................................................................
Fluorene .....................................................................................
Heptachlor ..................................................................................
206–44–0 .........
86–73–7 ...........
76–44–8 ...........
Heptachlor epoxide ....................................................................
1024–57–3 .......
Hexachlorobenzene ...................................................................
Hexachlorobutadiene .................................................................
Hexachlorocyclopentadiene .......................................................
Hexachloroethane ......................................................................
Hexachloropropene ....................................................................
2-Hexanone; Methyl butyl ketone ..............................................
Indeno(1,2,3-cd)pyrene ..............................................................
Isobutyl alcohol ..........................................................................
Isodrin ........................................................................................
118–74–1 .........
87–68–3 ...........
77–47–4 ...........
67–72–1 ...........
1888–71–7 .......
591–78–6 .........
193–39–5 .........
78–83–1 ...........
465–73–6 .........
Isophorone .................................................................................
Isosafrole ...................................................................................
Kepone .......................................................................................
78–59–1 ...........
120–58–1 .........
143–50–0 .........
Lead ...........................................................................................
Mercury ......................................................................................
Methacrylonitrile .........................................................................
Methapyrilene ............................................................................
(Total) ...............
(Total) ...............
126–98–7 .........
91–80–5 ...........
Methoxychlor ..............................................................................
Methyl bromide; Bromomethane ...............................................
Methyl chloride; Chloromethane ................................................
3-Methylcholanthrene ................................................................
Methyl ethyl ketone; MEK; 2-Butanone .....................................
Methyl iodide; Iodomethane ......................................................
Methyl methacrylate ...................................................................
Methyl methanesulfonate ...........................................................
2-Methylnaphthalene .................................................................
Methyl parathion; Parathion methyl ...........................................
72–43–5 ...........
74–83–9 ...........
74–87–3 ...........
56–49–5 ...........
78–93–3 ...........
74–88–4 ...........
80–62–6 ...........
66–27–3 ...........
91–57–6 ...........
298–00–0 .........
1,2-Benzenedicarboxylic acid, diethyl ester
Phosphorothioic acid, O,O-diethyl O-pyrazinyl ester.
Phosphorodithioic acid, O,O-dimethyl S-[2-(methylamino)-2oxoethyl] ester
Benzenamine, N,N-dimethyl-4-(phenylazo)Benz[a]anthracene, 7,12-dimethyl[1,1′-Biphenyl]-4,4′-diamine, 3,3′-dimethylBenzeneethanamine,aa-dimethy1
Phenol, 2,4-dimethyl1,2-Benzenedicarboxylic acid, dimethyl ester
Benzene, 1,3-dinitroPhenol, 2-methyl-4,6-dinitroPhenol, 2,4-dinitroBenzene, 1-methyl-2,4-dinitroBenzene, 2-methyl-1,3-dinitroPhenol, 2-(1-methylpropyl)-4,6-dinitro1,2-Benzenedicarboxylic acid, dioctyl ester
Benzenamine, N-phenylPhosphorodithioic acid, O,O-diethyl S-[2- (ethylthio)ethyl]
ester
6,9-Methano-2,4,3-benzodiox-athiepin,
6,7,8,9,10,10hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide,
6,9-Methano-2,4,3-benzodioxathiepin,
6,7,8,9,10,10hexachloro- 1,5,5a,6,9,9a-hexahydro-, 3-oxide, (3a,5aa,
6b,9b, 9aa)6,9-Methano-2,4,3-benzodioxathiepin,
6,7,8,9,10,10hexachloro-1,5,5a,6,9,9a-hexahydro-, 3,3-dioxide
2,7:3,6-Dimethanonaphth[2,3-b]oxirene,
3,4,5,6,9,9hexachloro-1a,2,2a,3,6,6a,7,7a-octahydro-, (1aa, 2b,2ab,
3a,6a,6ab,7b,7aa)1,2,4-Methenocyclo-penta[cd]pentalene-5carboxaldehyde,2,2a,3,3,4,7-hexachlorodecahydro(1a,2b,2ab,4b,4ab,5b,6ab,6bb,7R*)Benzene, ethyl2-Propenoic acid, 2-methyl-, ethyl ester
Methanesulfonic acid, ethyl ester
Phosphorothioic acid, O-[4-[(dimethylamino)sulfonyl]phenyl]O,O-dimethyl ester
Fluoranthene
9H-Fluorene
4,7-Methano-1H-indene,1,4,5,6,7,8,8-heptachloro-3a,4,7,7atetrahydro2,5-Methano-2H-indeno[1,2-b]oxirene,
2,3,4,5,6,7,7-heptachlor-1a,1b,5,5a,6,6a,-hexahydr-,(1aa,1bb,
2a,5a,5ab,6b,6aa)
Benzene, hexachloro1,3-Butadiene, 1,1,2,3,4,4-hexachloro1,3-Cyclopentadiene, 1,2,3,4,5,5-hexachloroEthane, hexachloro1-Propene, 1,1,2,3,3,3-hexachloro2-Hexanone
Indeno[1,2,3-cd]pyrene
1-Propanol, 2-methyl1,4,5,8-Dimethanonaphthalene,1,2,3,4,1
0,10-hexachloro1,4,4a,5,8,8a hexahydro-(1a, 4a, 4ab,5b,8b,8ab)2-Cyclohexen-1-one, 3,5,5-trimethyl1,3-Benzodioxole, 5-(1-propenyl)1,3,4-Metheno-2H-cyclobuta-[cd]pentalen-2-one,
1,1a,3,3a,4,5,5,5a,5b,6-decachlorooctahydroLead
Mercury
2-Propenenitrile, 2-methyl1,2,Ethanediamine,
N,N-dimethyl-N′-2-pyridinyl-N′-(2thienylmethyl)Benzene, 1,1′-(2,2,2,trichloroethylidene)bis [4-methoxyMethane, bromoMethane, chloroBenz[j]aceanthrylene, 1,2-dihydro-3-methyl2-Butanone
Methane, iodo2-Propenoic acid, 2-methyl-, methyl ester
Methanesulfonic acid, methyl ester
Naphthalene, 2-methylPhosphorothioic acid, O,O-dimethyl
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Common name 1
CAS RN 2
Chemical abstracts service index name 3
4-Methyl-2-pentanone; Methyl isobutyl ketone ..........................
Methylene bromide; Dibromomethane ......................................
Methylene chloride; Dichloromethane .......................................
Naphthalene ...............................................................................
1,4-Naphthoquinone ..................................................................
1-Naphthylamine ........................................................................
2-Naphthylamine ........................................................................
Nickel .........................................................................................
o-Nitroaniline; 2-Nitroaniline ......................................................
m-Nitroaniline; 3-Nitroaniline .....................................................
p-Nitroaniline; 4-Nitroaniline ......................................................
Nitrobenzene ..............................................................................
o-Nitrophenol; 2-Nitrophenol ......................................................
p-Nitrophenol; 4-Nitrophenol ......................................................
N-Nitrosodi-n-butylamine ...........................................................
N-Nitrosodiethylamine ................................................................
N-Nitrosodimethylamine .............................................................
N-Nitrosodiphenylamine .............................................................
N-Nitrosodipropylamine;
N-Nitroso-N-dipropylamine;
Di-npropylnitrosamine.
N-Nitrosomethylethalamine ........................................................
N-Nitrosopiperidine ....................................................................
N-Nitrosopyrrolidine ...................................................................
5-Nitro-o-toluidine ......................................................................
Parathion ....................................................................................
Pentachlorobenzene ..................................................................
Pentachloronitrobenzene ...........................................................
Pentachlorophenol .....................................................................
Phenacetin .................................................................................
Phenanthrene ............................................................................
Phenol ........................................................................................
p-Phenylenediamine ..................................................................
Phorate ......................................................................................
108–10–1 .........
74–95–3 ...........
75–09–2 ...........
91–20–3 ...........
130–15–4 .........
134–32–7 .........
91–59–8 ...........
(Total) ...............
88–74–4 ...........
99–09–2 ...........
100–01–6 .........
98–95–3 ...........
88–75–5 ...........
100–02–7 .........
924–16–3 .........
55–18–5 ...........
62–75–9 ...........
86–30–6 ...........
621–64–7 .........
2-Pentanone, 4-methylMethane, dibromoMethane, dichloroNaphthalene
1,4-Naphthalenedione
1-Naphthalenamine
2-Naphthalenamine
Nickel
Benzenamine, 2-nitroBenzenamine, 3-nitroBenzenamine, 4-nitroBenzene, nitroPhenol, 2-nitroPhenol, 4-nitro1-Butanamine, N-butyl-N-nitrosoEthanamine, N-ethyl-N-nitrosoMethanamine, N-methyl-N-nitrosoBenzenamine, N-nitroso-N-phenyl1-Propanamine, N-nitroso-N-propyl-
10595–95–6 .....
100–75–4 .........
930–55–2 .........
99–55–8 ...........
56–38–2 ...........
608–93–5 .........
82–68–8 ...........
87–86–5 ...........
62–44–2 ...........
85–01–8 ...........
108–95–2 .........
106–50–3 .........
298–02–2 .........
Polychlorinated biphenyls; PCBs ...............................................
Pronamide ..................................................................................
Propionitrile; Ethyl cyanide ........................................................
Pyrene ........................................................................................
Safrole ........................................................................................
Selenium ....................................................................................
Silver ..........................................................................................
Silvex; 2,4,5-TP .........................................................................
Styrene .......................................................................................
Sulfide ........................................................................................
2,4,5-T; 2,4,5-Trichlorophenoxyacetic acid ...............................
2,3,7,8-TCDD; 2,3,7,8-Tetrachlorodibenzo- p-dioxin .................
1,2,4,5-Tetrachlorobenzene .......................................................
1,1,1,2-Tetrachloroethane ..........................................................
1,1,2,2-Tetrachloroethane ..........................................................
Tetrachloroethylene; Tetrachloroethene; Perchloroethylene .....
2,3,4,6-Tetrachlorophenol ..........................................................
Thallium .....................................................................................
Tin ..............................................................................................
Toluene ......................................................................................
o-Toluidine .................................................................................
Toxaphene .................................................................................
1,2,4-Trichlorobenzene ..............................................................
1,1,1-Trichloroethane; Methylchloroform ...................................
1,1,2-Trichloroethane .................................................................
Trichloroethylene; Trichloroethene ............................................
Trichlorofluoromethane; CFC–11 ..............................................
2,4,5-Trichlorophenol .................................................................
2,4,6-Trichlorophenol .................................................................
1,2,3-Trichloropropane ...............................................................
O,O,O-Triethyl phosphorothioate ...............................................
sym-Trinitrobenzene ..................................................................
Vanadium ...................................................................................
Vinyl acetate ..............................................................................
Vinyl chloride; Chloroethene ......................................................
Xylene (total) ..............................................................................
Zinc ............................................................................................
See footnote 6 ..
23950–58–5 .....
107–12–0 .........
129–00–0 .........
94–59–7 ...........
(Total) ...............
(Total) ...............
93–72–1 ...........
100–42–5 .........
18496–25–8 .....
93–76–5 ...........
1746–01–6 .......
95–94–3 ...........
630–20–6 .........
79–34–5 ...........
127–18–4 .........
58–90–2 ...........
(Total) ...............
(Total) ...............
108–88–3 .........
95–53–4 ...........
See footnote 7 ..
120–82–1 .........
71–55–6 ...........
79–00–5 ...........
79–01–6 ...........
75–69–4 ...........
95–95–4 ...........
88–06–2 ...........
96–18–4 ...........
126–68–1 .........
99–35–4 ...........
(Total) ...............
108–05–4 .........
75–01–4 ...........
See footnote 8 ..
(Total) ...............
Ethanamine, N-methyl-N-nitrosoPiperidine, 1-nitrosoPyrrolidine, 1-nitrosoBenzenamine, 2-methyl-5-nitroPhosphorothioic acid, O,O-diethyl-O-(4-nitrophenyl) ester
Benzene, pentachloroBenzene, pentachloronitroPhenol, pentachloroAcetamide, N-(4-ethoxyphenyl)
Phenanthrene
Phenol
1,4-Benzenediamine
Phosphorodithioic acid, O,O-diethyl S- [(ethylthio)methyl]
ester
1,1′-Biphenyl, chloro derivatives
Benzamide, 3,5-dichloro-N-(1,1-dimethyl-2-propynyl)Propanenitrile
Pyrene
1,3-Benzodioxole, 5-(2- propenyl)Selenium
Silver
Propanoic acid, 2-(2,4,5- trichlorophenoxy)Benzene, ethenylSulfide
Acetic acid, (2,4,5- trichlorophenoxy)Dibenzo[b,e][1,4]dioxin, 2,3,7,8-tetrachloroBenzene, 1,2,4,5-tetrachloroEthane, 1,1,1,2-tetrachloroEthane, 1,1,2,2-tetrachloroEthene, tetrachloroPhenol, 2,3,4,6-tetrachloroThallium
Tin
Benzene, methylBenzenamine, 2-methylToxaphene
Benzene, 1,2,4-trichloroEthane, 1,1,1-trichloroEthane, 1,1,2-trichloroEthene, trichloroMethane, trichlorofluoroPhenol, 2,4,5-trichloroPhenol, 2,4,6-trichloroPropane, 1,2,3-trichloroPhosphorothioic acid, O,O,O-triethyl ester
Benzene, 1,3,5-trinitroVanadium
Acetic acid, ethenyl ester
Ethene, chloroBenzene, dimethylZinc
1 Common names are those widely used in government regulations, scientific publications, and commerce; synonyms exist for many chemicals.
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2 Chemical
Abstracts Service registry number. Where ‘‘Total’’ is entered, all species in the ground water that contain this element are included.
index names are those used in the 9th Cumulative Index.
substance is often called bis(2-chloroisopropyl) ether, the name Chemical Abstracts Service applies to its noncommercial isomer, propane, 2,2″-oxybis[2-chloro-(CAS RN 39638–32–9).
5 Chlordane: This entry includes alpha-chlordane (CAS RN 5103–71–9), beta-chlordane (CAS RN 5103–74–2), gamma-chlordane (CAS RN
5566–34–7), and constituents of chlordane (CAS RN 57–74–9 and CAS RN 12789–03–6).
6 Polychlorinated biphenyls (CAS RN 1336–36–3); this category contains congener chemicals, including constituents of Aroclor-1016 (CAS RN
12674–11–2), Aroclor-1221 (CAS RN 11104–28–2), Aroclor-1232 (CAS RN 11141–16–5), Aroclor-1242 (CAS RN 53469–21–9), Aroclor-1248
(CAS RN 12672–29–6), Aroclor-1254 (CAS RN 11097–69–1), and Aroclor-1260 (CAS RN 11096–82–5).
7 Toxaphene: This entry includes congener chemicals contained in technical toxaphene (CAS RN 8001–35–2), i.e., chlorinated camphene.
8 Xylene (total): This entry includes o-xylene (CAS RN 96–47–6), m-xylene (CAS RN 108–38–3), p-xylene (CAS RN 106–42–3), and unspecified xylenes (dimethylbenzenes) (CAS RN 1330–20–7).
3 CAS
4 This
PART 260—HAZARDOUS WASTE
MANAGEMENT SYSTEM: GENERAL
7. The authority citation for part 260
continues to read as follows:
I
Authority: 42 U.S.C. 6905, 6912(a), 6921–
6927, 6930, 6934, 6935, 6937, 6938, 6939,
and 6974.
Subpart B—Definitions
8. Section 260.11 is revised to read as
follows:
I
§ 260.11
References.
(a) When used in parts 260 through
270 of this chapter, the following
publications are incorporated by
reference. These incorporations by
reference were approved by the Director
of the Federal Register pursuant to 5
U.S.C. 552(a) and 1 CFR part 51. These
materials are incorporated as they exist
on the date of approval and a notice of
any change in these materials will be
published in the Federal Register.
Copies may be inspected at the Library,
U.S. Environmental Protection Agency,
1200 Pennsylvania Ave., NW. (3403T),
Washington, DC 20460,
libraryhq@epa.gov; or at the National
Archives and Records Administration
(NARA). For information on the
availability of this material at NARA,
call 202–741–6030, or go to: https://
www.archives.gov/federal_register/
code_of_federal_regulations/
ibr_locations.html.
(b) The following materials are
available for purchase from the
American Society for Testing and
Materials, 100 Barr Harbor Drive, P.O.
Box C700, West Conshohocken, PA
19428–2959.
(1) ASTM D–93–79 or D–93–80, ‘‘Standard
Test Methods for Flash Point by PenskyMartens Closed Cup Tester,’’ IBR approved
for § 261.21.
(2) ASTM D–1946–82, ‘‘Standard Method
for Analysis of Reformed Gas by Gas
Chromatography,’’ IBR approved for
§§ 264.1033, 265.1033.
(3) ASTM D 2267–88, ‘‘Standard Test
Method for Aromatics in Light Naphthas and
Aviation Gasolines by Gas Chromatography,’’
IBR approved for § 264.1063.
(4) ASTM D 2382–83, ‘‘Standard Test
Method for Heat of Combustion of
Hydrocarbon Fuels by Bomb Calorimeter
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(High-Precision Method),’’ IBR approved for
§§ 264.1033, 265.1033.
(5) ASTM D 2879–92, ‘‘Standard Test
Method for Vapor Pressure—Temperature
Relationship and Initial Decomposition
Temperature of Liquids by Isoteniscope,’’ IBR
approved for § 265.1084.
(6) ASTM D–3278–78, ‘‘Standard Test
Methods for Flash Point for Liquids by
Setaflash Closed Tester,’’ IBR approved for
§ 261.21(a).
(7) ASTM E 168–88, ‘‘Standard Practices
for General Techniques of Infrared
Quantitative Analysis,’’ IBR approved for
§ 264.1063.
(8) ASTM E 169–87, ‘‘Standard Practices
for General Techniques of Ultraviolet-Visible
Quantitative Analysis,’’ IBR approved for
§ 264.1063.
(9) ASTM E 260–85, ‘‘Standard Practice for
Packed Column Gas Chromatography,’’ IBR
approved for § 264.1063.
(10) ASTM E 926–88, ‘‘Standard Test
Methods for Preparing Refuse-Derived Fuel
(RDF) Samples for Analyses of Metals,’’ Test
Method C—Bomb, Acid Digestion Method.
(c) The following materials are
available for purchase from the National
Technical Information Service, 5285
Port Royal Road, Springfield, VA 22161;
or for purchase from the Superintendent
of Documents, U.S. Government
Printing Office, Washington, DC 20402,
(202) 512–1800.
(1) ‘‘APTI Course 415: Control of Gaseous
Emissions,’’ EPA Publication EPA–450/2–81–
005, December 1981, IBR approved for
§§ 264.1035, 265.1035, 270.24, 270.25.
(2) Method 1664, Revision A, n-Hexane
Extractable Material (HEM; Oil and Grease)
and Silica Gel Treated n-Hexane Extractable
Material (SGT–HEM; Non-polar Material) by
Extraction and Gravimetry, PB99–121949,
IBR approved for part 261, appendix IX.
(3) The following methods as published in
the test methods compendium known as
‘‘Test Methods for Evaluating Solid Waste,
Physical/Chemical Methods,’’ EPA
Publication SW–846, Third Edition. A suffix
of ‘‘A’’ in the method number indicates
revision one (the method has been revised
once). A suffix of ‘‘B’’ in the method number
indicates revision two (the method has been
revised twice). A suffix of ‘‘C’’ in the method
number indicates revision three (the method
has been revised three times). A suffix of ‘‘D’’
in the method number indicates revision four
(the method has been revised four times).
(i) Method 0010, dated September 1986
and in the Basic Manual, IBR approved for
part 261, appendix IX.
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(ii) Method 0020, dated September 1986
and in the Basic Manual, IBR approved for
part 261, appendix IX.
(iii) Method 0030, dated September 1986
and in the Basic Manual, IBR approved for
part 261, appendix IX.
(iv) Method 1320, dated September 1986
and in the Basic Manual, IBR approved for
part 261, appendix IX.
(v) Method 1311, dated September 1992
and in Update I, IBR approved for part 261,
appendix IX, and §§ 261.24, 268.7, 268.40.
(vi) Method 1330A, dated September 1992
and in Update I, IBR approved for part 261,
appendix IX.
(vii) Method 1312 dated September 1994
and in Update II, IBR approved for part 261,
appendix IX.
(viii) Method 0011, dated December 1996
and in Update III, IBR approved for part 261,
appendix IX, and part 266, appendix IX.
(ix) Method 0023A, dated December 1996
and in Update III, IBR approved for part 261,
appendix IX, part 266, appendix IX, and
§ 266.104.
(x) Method 0031, dated December 1996 and
in Update III, IBR approved for part 261,
appendix IX.
(xi) Method 0040, dated December 1996
and in Update III, IBR approved for part 261,
appendix IX.
(xii) Method 0050, dated December 1996
and in Update III, IBR approved for part 261,
appendix IX, part 266, appendix IX, and
§ 266.107.
(xiii) Method 0051, dated December 1996
and in Update III, IBR approved for part 261,
appendix IX, part 266, appendix IX, and
§ 266.107.
(xiv) Method 0060, dated December 1996
and in Update III, IBR approved for part 261,
appendix IX, § 266.106, and part 266,
appendix IX.
(xv) Method 0061, dated December 1996
and in Update III, IBR approved for part 261,
appendix IX, § 266.106, and part 266,
appendix IX.
(xvi) Method 9071B, dated April 1998 and
in Update IIIA, IBR approved for part 261,
appendix IX.
(xvii) Method 1010A, dated November
2004 and in Update IIIB, IBR approved for
part 261, appendix IX.
(xviii) Method 1020B, dated November
2004 and in Update IIIB, IBR approved for
part 261, appendix IX.
(xix) Method 1110A, dated November 2004
and in Update IIIB, IBR approved for § 261.22
and part 261, appendix IX.
(xx) Method 1310B, dated November 2004
and in Update IIIB, IBR approved for part
261, appendix IX.
(xxi) Method 9010C, dated November 2004
and in Update IIIB, IBR approved for part
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261, appendix IX and §§ 268.40, 268.44,
268.48.
(xxii) Method 9012B, dated November
2004 and in Update IIIB, IBR approved for
part 261, appendix IX and §§ 268.40, 268.44,
268.48.
(xxiii) Method 9040C, dated November
2004 and in Update IIIB, IBR approved for
part 261, appendix IX and § 261.22.
(xxiv) Method 9045D, dated November
2004 and in Update IIIB, IBR approved for
part 261, appendix IX.
(xxv) Method 9060A, dated November
2004 and in Update IIIB, IBR approved for
part 261, appendix IX, and §§ 264.1034,
264.1063, 265.1034, 265.1063.
(xxvi) Method 9070A, dated November
2004 and in Update IIIB, IBR approved for
part 261, appendix IX.
(xxvii) Method 9095B, dated November
2004 and in Update IIIB, IBR approved, part
261, appendix IX, and §§ 264.190, 264.314,
265.190, 265.314, 265.1081, 268.32.
Subpart C—Rulemaking Petitions
(d) The following materials are
available for purchase from the National
Fire Protection Association, 1
Batterymarch Park, P.O. Box 9101,
Quincy, MA 02269–9101.
§ 260.22 Petitions to amend part 261 to
exclude a waste produced at a particular
facility.
(1) ‘‘Flammable and Combustible Liquids
Code’’ (1977 or 1981), IBR approved for
§§ 264.198, 265.198.
(2) [Reserved]
(e) The following materials are
available for purchase from the
American Petroleum Institute, 1220 L
Street, Northwest, Washington, DC
20005.
(1) API Publication 2517, Third Edition,
February 1989, ‘‘Evaporative Loss from
External Floating-Roof Tanks,’’ IBR approved
for § 265.1084.
(2) [Reserved]
(f) The following materials are
available for purchase from the
Environmental Protection Agency,
Research Triangle Park, NC.
(1) OECD Green List of Wastes (revised
May 1994), Amber List of Wastes and Red
List of Wastes (both revised May 1993) as set
forth in Appendix 3, Appendix 4 and
Appendix 5, respectively, to the OECD
Council Decision C(92)39/FINAL
(Concerning the Control of Transfrontier
Movements of Wastes Destined for Recovery
Operations), IBR approved for 262.89 of this
chapter.
(2) [Reserved]
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*
*
*
*
*
(d) If the Administrator amends the
regulations to permit use of a new
testing method, the method will be
incorporated by reference in § 260.11
and added to ‘‘Test Methods for
Evaluating Solid Waste, Physical/
Chemical Methods,’’ EPA Publication
SW–846, U.S. Environmental Protection
Agency, Office of Solid Waste,
Washington, DC 20460.
I 10. Section 260.22 is amended by
revising paragraph (d)(1)(i) to read as
follows:
*
*
*
*
*
(d) * * *
(1) * * *
(i) Does not contain the constituent or
constituents (as defined in Appendix
VII of part 261 of this chapter) that
caused the Administrator to list the
waste; or
*
*
*
*
*
Subpart C—Characteristics of
Hazardous Waste
13. Section 261.21 is amended by
revising paragraph (a)(1) to read as
follows:
I
§ 261.21
Characteristic of ignitability.
(a) * * *
(1) It is a liquid, other than an
aqueous solution containing less than
24 percent alcohol by volume and has
flash point less than 60 °C (140 °F), as
determined by a Pensky-Martens Closed
Cup Tester, using the test method
specified in ASTM Standard D 93–79 or
D 93–80 (incorporated by reference, see
§ 260.11), or a Setaflash Closed Cup
Tester, using the test method specified
in ASTM Standard D 3278–78
(incorporated by reference, see
§ 260.11).
*
*
*
*
*
I 14. Section 261.22 is amended by
revising paragraphs (a)(1) and (2) to read
as follows:
§ 261.22
Characteristic of corrosivity.
12. Section 261.3 is amended by
revising paragraph (a)(2)(v) introductory
text to read as follows:
(a) * * *
(1) It is aqueous and has a pH less
than or equal to 2 or greater than or
equal to 12.5, as determined by a pH
meter using Method 9040C in ‘‘Test
Methods for Evaluating Solid Waste,
Physical/Chemical Methods,’’ EPA
Publication SW–846, as incorporated by
reference in § 260.11 of this chapter.
(2) It is a liquid and corrodes steel
(SAE 1020) at a rate greater than 6.35
mm (0.250 inch) per year at a test
temperature of 55 °C (130 °F) as
determined by Method 1110A in ‘‘Test
Methods for Evaluating Solid Waste,
Physical/Chemical Methods,’’ EPA
Publication SW–846, and as
incorporated by reference in § 260.11 of
this chapter.
*
*
*
*
*
§ 261.3
Subpart D—Lists of Hazardous Wastes
PART 261—IDENTIFICATION AND
LISTING OF HAZARDOUS WASTE
11. The authority citation for part 261
continues to read as follows:
I
Authority: 42 U.S.C. 6905, 6912(a), 6921,
6922, 6924(y), and 6938.
I
(g) The following materials are
available for purchase from the
Organisation for Economic Co-operation
and Development, Environment
Direcorate, 2 rue Andre Pascal, 75775
Paris Cedex 16, France.
20:19 Jun 13, 2005
§ 260.21 Petitions for equivalent testing or
analytical methods.
Subpart A—General
(1) ‘‘Screening Procedures for Estimating
the Air Quality Impact of Stationary Sources,
Revised’’, October 1992, EPA Publication No.
EPA–450/R–92–019, IBR approved for part
266, appendix IX.
(2) [Reserved]
VerDate jul<14>2003
9. Section 260.21 is amended by
revising paragraph (d) to read as follows:
I
34561
Definition of hazardous waste.
(a) * * *
(2) * * *
(v) Rebuttable presumption for used
oil. Used oil containing more than 1000
ppm total halogens is presumed to be a
hazardous waste because it has been
mixed with halogenated hazardous
waste listed in subpart D of part 261 of
this chapter. Persons may rebut this
presumption by demonstrating that the
used oil does not contain hazardous
waste (for example, to show that the
used oil does not contain significant
concentrations of halogenated
hazardous constituents listed in
appendix VIII of part 261 of this
chapter).
*
*
*
*
*
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15. Section 261.35 is amended by
revising paragraphs (b)(2)(iii)(A) and (B)
to read as follows:
I
§ 261.35 Deletion of certain hazardous
waste codes following equipment cleaning
and replacement.
*
*
*
*
*
(b) * * *
(2) * * *
(iii) * * *
(A) Rinses must be tested by using an
appropriate method.
(B) ‘‘Not detected’’ means at or below
the following lower method calibration
limits (MCLs): The 2,3,7,8-TCDD-based
MCL—0.01 parts per trillion (ppt),
sample weight of 1000 g, IS spiking
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level of 1 ppt, final extraction volume of
10–50 µL. For other congeners—
multiply the values by 1 for TCDF/
PeCDD/PeCDF, by 2.5 for HxCDD/
HxCDF/HpCDD/HpCDF, and by 5 for
OCDD/OCDF.
*
*
*
*
*
I 16. Section 261.38 is amended by
revising paragraph (c)(7) introductory
text to read as follows:
§ 261.38 Comparable/Syngas Fuel
Exclusion.
*
*
*
*
*
(c) * * *
(7) Waste analysis plans. The
generator of a comparable/syngas fuel
shall develop and follow a written waste
analysis plan which describes the
procedures for sampling and analysis of
the hazardous waste to be excluded. The
plan shall be followed and retained at
the facility excluding the waste.
*
*
*
*
*
I 17. Appendix I to part 261 is amended
by revising paragraphs four and five to
read as follows:
Appendix I to Part 261—Representative
Sampling Methods
*
*
*
*
*
Containerized liquid waste—
‘‘COLIWASA.’’
Liquid waste in pits, ponds, lagoons,
and similar reservoirs.—‘‘Pond
Sampler.’’
*
*
*
*
*
Appendices II and III to Part 261
[Removed and Reserved]
18. Part 261 is amended by removing
and reserving Appendices II and III.
I
19. Appendix IX to part 261 is
amended in Table 1:
I a. In the entry for ‘‘Aptus, Inc,
Coffeyville, Kansas,’’ under the ‘‘Waste
description’’ column, by revising
paragraphs (2), (3), and (4);
I b. In the entry for ‘‘Arkansas
Department of Pollution Control and
Ecology, Vertac Superfund site,
Jacksonville, Arkansas,’’ under the
‘‘Waste description’’ column, by revising
the introductory text of paragraph (1) and
by revising paragraph (3)(C);
I c. In the entry for ‘‘Bekaert Corp.,
Dyersburg, TN,’’ under the ‘‘Waste
description’’ column, by revising
paragraph (4)(B);
I d. In the entry for ‘‘Bethlehem Steel
Corporation, Sparrows Point,
Maryland,’’ under the ‘‘Waste
description’’ column, by revising the
introductory text of paragraph (1);
I e. In the entry for ‘‘BMW
Manufacturing Corporation, Greer,
South Carolina,’’ under the ‘‘Waste
description’’ column, by revising the
introductory text of paragraph (2);
I f. In the entry for ‘‘DuraTherm,
Incorporated, San Leon, Texas,’’ under
the ‘‘Waste description’’ column, by
revising the introductory text of
paragraph (3);
I g. In the entry for ‘‘Eastman Chemical
Company, Longview, Texas,’’ under the
‘‘Waste description’’ column, by revising
the introductory text of paragraph (3);
I h. In the entry for ‘‘Envirite of
Pennsylvania (formerly Envirite
Corporation), York, Pennsylvania,’’
under the ‘‘Waste description’’ column,
by revising paragraph (2);
I i. In the entry for ‘‘Geological
Reclamation Operations and Waste
I
Systems, Inc., Morrisville, PA,’’ under
the ‘‘Waste description’’ column, by
revising the introductory text of
paragraph (1);
I j. In the entry for ‘‘McDonnell Douglas
Corporation, Tulsa, Oklahoma,’’ under
the ‘‘Waste description’’ column, by
revising paragraph (3);
I k. In the entry for ‘‘Occidental
Chemical, Ingleside, Texas,’’ under the
‘‘Waste description’’ column, by revising
the introductory text of paragraph (3);
I l. By removing the entry for
‘‘OxyVinyls, L.P., Deer Park, TX;’’
I m. In the entry for ‘‘Rhodia, Houston,
Texas,’’ under the ‘‘Waste description’’
column, by revising the introductory text
of paragraph (3);
I n. In the entry for ‘‘Syntex
Agribusiness, Springfield, MO,’’ under
the ‘‘Waste description’’ column, by
revising paragraphs (2), (3), (4), (5), and
(6);
I o. In the entry for ‘‘Texas Eastman,
Longview, Texas,’’ under the ‘‘Waste
description’’ column, by revising
paragraph 3;
I p. In the entry for ‘‘Tokusen USA, Inc.,
Conway, AR,’’ under the ‘‘Waste
description’’ column, by revising
paragraph (2)(C), the introductory text of
paragraph (3), and paragraphs (3)(A)(ii),
(3)(B), and (3)(C)(ii);
I q. In the entry for ‘‘Tyco Printed
Circuit Group, Melbourne Division,
Melbourne, Florida,’’ under the ‘‘Waste
description’’ column, by revising the
introductory text of paragraph (1).
The revisions read as follows:
Appendix IX to Part 261—Wastes
Excluded Under §§ 260.20 and 260.22
TABLE 1.—WASTES EXCLUDED FROM NON-SPECIFIC SOURCES
Facility
Address
*
*
Aptus, Inc ....................................
*
Coffeyville, Kansas ......................
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TABLE 1.—WASTES EXCLUDED FROM NON-SPECIFIC SOURCES—Continued
Facility
Address
Waste description
(2) A minimum of four grab samples must be taken from each hopper (or
other container) of kiln residue generated during each 24-hour run; all
grabs collected during a given 24-hour run must then be composited to
form one composite sample. A minimum of four grab samples must
also be taken from each hopper (or other container) of spray dryer/
baghouse residue generated during each 24-hour run; all grabs collected during a given 24-hour run must then be composited to form
one composite sample. Prior to the disposal of the residues from each
24-hour run, a TCLP leachate test must be performed on these composite samples and the leachate analyzed for the TC toxic metals,
nickel, and cyanide. If arsenic, chromium, lead or silver TC leachate
test results exceed 1.6 ppm, barium levels exceed 32 ppm, cadmium
or selenium levels exceed 0.3 ppm, mercury levels exceed 0.07 ppm,
nickel levels exceed 10 ppm, or cyanide levels exceed 6.5 ppm, the
wastes must be retreated to achieve these levels or must be disposed
in accordance with subtitle C of RCRA. Analyses must be performed
according to appropriate methods. As applicable to the method-defined
parameters of concern, analyses requiring use of SW–846 methods incorporated by reference in 40 CFR 260.11 must be used without substitution. As applicable, the SW–846 methods might include Methods
0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061,
1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C,
9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev.
A), 9071B, and 9095B.
(3) Aptus must generate, prior to the disposal of the residues, verification
data from each 24 hour run for each treatment residue (i.e., kiln residue, spray dryer/baghouse residue) to demonstrate that the maximum
allowable treatment residue concentrations listed below are not exceeded. Samples must be collected as specified in Condition (2). Analyses must be performed according to appropriate methods. As applicable to the method-defined parameters of concern, analyses requiring
the use of SW–846 methods incorporated by reference in 40 CFR
260.11 must be used without substitution. As applicable, the SW–846
methods might include Methods 0010, 0011, 0020, 0023A, 0030, 0031,
0040, 0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311,
1312, 1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A, 9070A
(uses EPA Method 1664, Rev. A), 9071B, and 9095B. Any residues
which exceed any of the levels listed below must be retreated or must
be disposed of as hazardous. Kiln residue and spray dryer/baghouse
residue must not exceed the following levels:
Aldrin—0.015 ppm, Benzene—9.7 ppm, Benzo(a)pyrene—0.43 ppm,
Benzo(b)fluoranthene)—1.8 ppm, Chlordane—0.37 ppm, Chloroform—
5.4 ppm, Chrysene—170 ppm, Dibenz(a,h)anthracene—0.083 ppm,
1.2-Dichloroethane—4.1 ppm, Dichloromethane—2.4 ppm, 2,4Dichlorophenol—480 ppm, Dichlorvos—260 ppm, Disulfaton—23 ppm,
Endosulfan I—310 ppm, Fluorene—120 ppm, Indeno(1,2,3,cd)-pyrene—330 ppm, Methyl parathion—210 ppm, Nitrosodiphenylamine—
130 ppm, Phenanthrene—150 ppm, Polychlorinated biphenyls—0.31
ppm, Tetrachlorethylene—59 ppm, 2,4,5-TP (silvex)—110 ppm, 2,4,6Trichlorophenol—3.9 ppm.
(4) Aptus must generate, prior to disposal of residues, verification data
from each 24-hour run for each treatment residue (i.e., kiln residue,
spray dryer/baghouse residue) to demonstrate that the residues do not
contain tetra-, penta-, or hexachlorodibenzo-p-dioxins or furans at levels of regulatory concern. Samples must be collected as specified in
Condition (2). The TCDD equivalent levels for the solid residues must
be less than 5 ppt. Any residues with detected dioxins or furans in excess of this level must be retreated or must be disposed of as acutely
hazardous. For tetra- and penta-chlorinated dioxin and furan homologs,
the maximum practical quantitation limit must not exceed 15 ppt for the
solid residues. For hexachlorinated dioxin and furan homologs, the
maximum practical quantitation limit must not exceed 37 ppt for the
solid residues.
* * * * *
*
*
Arkansas Department of Pollution
Control and Ecology.
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*
Vertac Superfund site, Jacksonville, Arkansas.
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TABLE 1.—WASTES EXCLUDED FROM NON-SPECIFIC SOURCES—Continued
Facility
Address
Waste description
(1) Testing: Sample collection and analyses (including quality control
(QC) procedures) must be performed according to appropriate methods. As applicable to the method-defined parameters of concern, analyses requiring the use of SW–846 methods incorporated by reference
in 40 CFR 260.11 must be used without substitution. As applicable, the
SW–846 methods might include Methods 0010, 0011, 0020, 0023A,
0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A, 1020B, 1110A,
1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B, 9040C, 9045D,
9060A, 9070A (uses EPA Method 1664, Rev. A), 9071B, and 9095B.
* * * * *
(3) * * *
(C) Chlorinated dioxins and furans: 2,3,7,8-Tetrachlorodibenzo-p-dioxin
equivalents, 4 x 10-7 ppm. The petitioned by-product must be analyzed
for the tetra-, penta-, hexa-, and heptachlorodibenzo-p-dioxins, and the
tetra-, penta-, hexa-, and heptachlorodibenzofurans to determine the 2,
3, 7, 8-tetra-chlorodibenzo-p-dioxin equivalent concentration. The analysis must be conducted using a measurement system that achieves
practical quantitation limits of 15 parts per trillion (ppt) for the tetra- and
penta-homologs, and 37 ppt for the hexa- and hepta-homologs.
* * * * *
*
*
Bekaert Corp. ..............................
*
Dyersburg, TN .............................
Bethlehem Steel Corporation ......
Sparrows Point, Maryland ...........
BMW Manufacturing Corporation
Greer, South Carolina .................
*
*
DuraTherm, Incorporated ............
*
San Leon, Texas .........................
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*
*
*
*
* * * * *
(4) * * *
(A) * * *
(B) The sample for the annual testing shall be a representative composite sample for all constituents listed in paragraph (1).
* * * * *
(1) Testing: Sample collection and analyses (including quality control
(QC) procedures) must be performed using appropriate methods. As
applicable to the method-defined parameters of concern, analyses requiring the use of SW–846 methods incorporated by reference in 40
CFR 260.11 must be used without substitution. As applicable, the SW–
846 methods might include Methods 0010, 0011, 0020, 0023A, 0030,
0031, 0040, 0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B,
1311, 1312, 1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A,
9070A (uses EPA Method 1664, Rev. A), 9071B, and 9095B. If EPA
judges the stabilization process to be effective under the conditions
used during the initial verification testing, BSC may replace the testing
required in Condition (1)(A) with the testing required in Condition
(1)(B). BSC must continue to test as specified in Condition (1)(A) until
and unless notified by EPA in writing that testing in Condition (1)(A)
may be replaced by Condition (1)(B) (to the extent directed by EPA).
* * * * *
* * * * *
(2) Verification Testing Requirements: Sample collection and analyses,
including quality control procedures, must be performed using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. Methods must meet Performance Based Measurement System Criteria in which the Data Quality Objectives are to demonstrate that representative samples of the BMW Sludge meet the
delisting levels in Condition (1).
* * * * *
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* *
*
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TABLE 1.—WASTES EXCLUDED FROM NON-SPECIFIC SOURCES—Continued
Facility
Address
Waste description
Eastman Chemical Company ......
Longview, Texas .........................
*
*
Envirite of Pennsylvania (formerly
Envirite Corporation).
*
York, Pennsylvania .....................
(3) Verification Testing Requirements: DuraTherm must perform sample
collection and analyses, including quality control procedures, using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. If EPA judges the process to be effective under the
operating conditions used during the initial verification testing,
DuraTherm may replace the testing required in Paragraph (3)(A) with
the testing required in Paragraph (3)(B). DuraTherm must continue to
test as specified in Paragraph (3)(A) until and unless notified by EPA
in writing that testing in Paragraph (3)(A) may be replaced by Paragraph (3)(B).
* * * * *
* * * * *
(3) Verification Testing Requirements: Eastman must perform sample collection and analyses, including quality control procedures, using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. After completion of the initial verification period,
Eastman may replace the testing required in Condition (3)(A) with the
testing required in Condition (3)(B). Eastman must continue to test as
specified in Condition (3)(A) until and unless notified by EPA in writing
that testing in Condition (3)(A) may be replaced by Condition (3)(B).
* * * * *
*
* *
*
*
*
*
*
*
(2) Each batch of treatment residue must be tested for leachable cyanide.If the leachable cyanide levels (using the EP Toxicity test without
acetic acid adjustment) exceed 1.26 ppm, the waste must be re-treated
or managed and disposed as a hazardous waste under 40 CFR Parts
262 to 265 and the permitting standards of 40 CFR Part 270.
* * * * *
*
*
Geological Reclamation Operations and Systems, Inc.
*
Morrisville, Pennsylvania .............
*
* *
*
*
*
*
*
*
(1) Testing: Sample collection and analyses, including quality control
(QC) procedures, must be performed using appropriate methods. As
applicable to the method-defined parameters of concern, analyses requiring the use of SW–846 methods incorporated by reference in 40
CFR 260.11 must be used without substitution. As applicable, the SW–
846 methods might include Methods 0010, 0011, 0020, 0023A, 0030,
0031, 0040, 0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B,
1311, 1312, 1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A,
9070A (uses EPA Method 1664, Rev. A), 9071B, and 9095B.
* * * * *
*
*
McDonnell Douglas Corporation
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*
Tulsa, Oklahoma .........................
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TABLE 1.—WASTES EXCLUDED FROM NON-SPECIFIC SOURCES—Continued
Facility
Address
Waste description
(3) Verification Testing Requirements: Sample collection and analyses,
including quality control procedures, must be performed using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. McDonnell Douglas must stabilize the previously
unstabilized waste from the bottom portion of the northwest lagoon of
the surface impoundment (which was closed as a landfill) using fly ash,
kiln dust or similar accepted materials in batches of 500 cubic yards or
less. McDonnell Douglas must analyze one composite sample from
each batch of 500 cubic yards or less. A minimum of four grab samples must be taken from each waste pile (or other designated holding
area) of stabilized waste generated from each batch run. Each composited batch sample must be analyzed, prior to disposal of the waste
in the batch represented by that sample, for constituents listed in Condition (1). There are no verification testing requirements for the stabilized wastes in the upper portions of the northwest lagoon, the entire
northeast lagoon, and the entire south lagoon of the surface impoundments which were closed as a landfill.
* * * * *
*
*
Occidental Chemical ...................
*
Ingleside, Texas ..........................
*
*
*
*
* * * * *
(3) Verification Testing Requirements: Sample collection and analyses,
including quality control procedures, must be performed using appropriate methods. As applicable to the method-defined parameters of
concern, any analyses requiring use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must use those methods without substitution. As applicable, the SW–846 methods might include Methods
0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061,
1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C,
9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev.
A), 9071B, and 9095B. If EPA judges the incineration process to be effective under the operating conditions used during the initial verification
testing, Occidental Chemical may replace the testing required in Condition (3)(A) with the testing required in Condition (3)(B). Occidental
Chemical must continue to test as specified in Condition (3)(A) until
and unless notified by EPA in writing that testing in Condition (3)(A)
may be replaced by Condition (3)(B).
* * * * *
*
*
Rhodia .........................................
*
Houston, Texas ...........................
*
*
*
*
* * * * * *
(3) Verification Testing Requirements: Rhodia must perform sample collection and analyses, including quality control procedures, using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. If EPA judges the process to be effective under the
operating conditions used during the initial verification testing, Rhodia
may replace the testing required in Condition (3)(A) with the testing required in Condition (3)(B). Rhodia must continue to test as specified in
Condition (3)(A) until and unless notified by EPA in writing that testing
in Condition (3)(A) may be replaced by Condition (3)(B).
* * * * *
*
*
Syntex Agribusiness ....................
*
Springfield, MO ...........................
*
* *
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Facility
Address
Waste description
(2) Four grab samples of wastewater must be composited from the volume of filtered wastewater collected after each eight hour run and,
prior to disposal the composite samples must be analyzed for the EP
toxic metals, nickel, and cyanide. If arsenic, chromium, lead, and silver
EP leachate test results exceed 0.61 ppm; barium levels exceed 12
ppm; cadmium and selenium levels exceed 0.12 ppm; mercury levels
exceed 0.02 ppm; nickel levels exceed 6.1 ppm; or cyanide levels exceed 2.4 ppm, the wastewater must be retreated to achieve these levels or must be disposed in accordance with all applicable hazardous
waste regulations. Analyses must be performed using appropriate
methods. As applicable to the method- defined parameters of concern,
analyses requiring the use of SW–846 methods incorporated by reference in 40 CFR 260.11 must be used without substitution. As applicable, the SW–846 methods might include Methods 0010, 0011, 0020,
0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A, 1020B,
1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B, 9040C,
9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A), 9071B, and
9095B.
(3) One grab sample must be taken from each drum of kiln and cyclone
ash generated during each eight-hour run; all grabs collected during a
given eight-hour run must then be composited to form one composite
sample. A composite sample of four grab samples of the separator
sludge must be collected at the end of each eight-hour run. Prior to the
disposal of the residues from each eight-hour run, an EP leachate test
must be performed on these composite samples and the leachate analyzed for the EP toxic metals, nickel, and cyanide (using a distilled
water extraction for the cyanide extraction) to demonstrate that the following maximum allowable treatment residue concentrations listed
below are not exceeded. Analyses must be performed using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. Any residues which exceed any of the levels listed
below must be retreated to achieve these levels or must be disposed
in accordance with all applicable hazardous waste regulations.
Maximum Allowable Solids Treatment Residue EP Leachate Concentrations (mg/L)
Arsenic—1.6, Barium—32, Cadmium—0.32, Chromium—1.6, Lead—1.6,
Mercury—0.065, Nickel—16, Selenium—0.32, Silver—1.6, Cyanide—
6.5.
(4) If Syntex stabilizes any of the kiln and cyclone ash or separator
sludge, a Portland cement-type stabilization process must be used and
Syntex must collect a composite sample of four grab samples from
each batch of stabilized waste. An MEP leachate test must be performed on these composite samples and the leachate analyzed for the
EP toxic metals, nickel, and cyanide (using a distilled water extraction
for the cyanide leachate analysis) to demonstrate that the maximum allowable treatment residue concentrations listed in condition (3) are not
exceeded during any run of the MEP extraction. Analyses must be performed using appropriate methods. As applicable to the method-defined parameters of concern, analyses requiring the use of SW–846
methods incorporated by reference in 40 CFR 260.11 must be used
without substitution. As applicable, the SW–846 methods might include
Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051,
0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A,
9010C, 9012B, 9040C 9045D, 9060A, 9070A (uses EPA Method 1664,
Rev. A), 9071B, and 9095B. Any residues which exceed any of the
levels listed in Condition (3) must be retreated to achieve these levels
or must be disposed in accordance with all applicable hazardous waste
regulations. (If the residues are stabilized, the analyses required in this
condition supercede the analyses required in Condition (3).)
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TABLE 1.—WASTES EXCLUDED FROM NON-SPECIFIC SOURCES—Continued
Facility
Address
Waste description
(5) Syntex must generate, prior to disposal of residues, verification data
from each eight hour run from each treatment residue (i.e., kiln and cyclone ash, separator sludge, and filtered wastewater) to demonstrate
that the maximum allowable treatment residue concentrations listed
below are not exceeded. Samples must be collected as specified in
Conditions (2) and (3). Analyses must be performed using appropriate
methods. As applicable to the method-defined parameters of concern,
analyses requiring the use of SW–846 methods incorporated by reference in 40 CFR 260.11 must be used without substitution. As applicable, the SW–846 methods might include Methods 0010, 0011, 0020,
0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A, 1020B,
1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B, 9040C,
9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A), 9071B, and
9095B. Any solid or liquid residues which exceed any of the levels listed below must be retreated to achieve these levels or must be disposed in accordance with Subtitle C of RCRA. Maximum Allowable
Wastewater Concentrations (ppm):
Benz(a)anthracene—1 × 10-7, Benzo(a)pyrene—4 × 10-4, Chloroform—
0.07, Chrysene—0.002, Dibenz(a,h)anthracene—9 × 10-6, 1,2Dichloroethane—0.06,
Dichloromethane—0.06,
Indeno(1,2,3cd)pyrene—0.002, Polychlorinated biphenyls—1 × 10-4, 1,2,4,5Tetrachlorobenzene—0.13, 2,3,4,6-Tetrachlorophenol—12, Toluene—
120,
Trichloroethylene—0.04,
2,4,5-Trichlorophenol—49,
2,4,6Trichlorophenol—0.02, Maximum Allowable Solid Treatment Residue.
Concentrations (ppm); Benz(a)anthracene—1.1, Benzo(a)pyrene—0.43,
benzo(b)fluoranthene—1.8,
Chloroform—5.4,
Chrysene—170,
Dibenz(a,h)anthracene—0.083,
Dichloromethane—2.4,
1,2Dichloroethane—4.1, Indeno(1,2,3-cd)pyrene—330, Polychlorinated
biphenyls—0.31, 1,2,4,5-Tetrachlorobenzene—720, Trichloroethylene—
6.6, 2,4,6-Trichlorophenol—3.9.
(6) Syntex must generate, prior to disposal of residues, verification data
from each eight-hour run for each treatment residue (i.e., kiln and cyclone ash, separator sludge, and filtered wastewater) to demonstrate
that the residues do not contain tetra-, penta-, or hexachlorodibenzo-pdioxins or furans at levels of regulatory concern. Samples must be collected as specified in Conditions (2) and (3). The TCDD equivalent levels for wastewaters must be less than 2 ppq and less than 5 ppt for
the solid treatment residues. Any residues with detected dioxins or
furans in excess of these levels must be retreated or must be disposed
as acutely hazardous. For this analysis, Syntex must use appropriate
methods. For tetra- and pentachloronated dioxin and furan homologs,
the maximum practical quantitation limit must not exceed 15 ppt for
solids and 120 ppq for wastewaters. For hexachlorinated homologs,
the maximum practical quantitation limit must not exceed 37 ppt for
solids and 300 ppq for wastewaters.
* * * * *
*
*
Texas Eastman ...........................
*
Longview, Texas .........................
Tokusen USA, Inc. ......................
Conway, AR ................................
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(3) Verification Testing Requirements: Sample collection and analyses,
including quality control procedures, must be performed using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. If EPA judges the incineration process to be effective under the operating conditions used during the initial verification
testing described in Condition Texas Eastman may replace the testing
required in Condition (4) with the testing required in Condition (5)
below. Texas Eastman must, however, continue to test as specified in
Condition (4) until notified by EPA in writing that testing in Condition
(4) may be replaced by the testing described in Condition (5).
* * * * *
* * * * *
(2) * * *
(B) * * *
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Facility
Address
Waste description
(C) If constituent levels in a sample exceed any of the delisting levels set
in Paragraph (1), Tokusen must retreat the batches of waste used to
generate the representative sample until it meets the levels. Tokusen
must repeat the analyses of the treated waste.
(D) * * *
(3) Verification Testing Requirements: Tokusen must perform sample collection and analyses, including quality control procedures, using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. If EPA judges the process to be effective under the
operating conditions used during the initial verification testing, Tokusen
may replace the testing required in Paragraph (3)(A) with the testing
required in Paragraph (3)(B). Tokusen must continue to test as specified in Paragraph (3)(A) until and unless notified by EPA in writing that
testing in Paragraph (3)(A) may be replaced by Paragraph (3)(B).
(A) * * *
(i) * * *
* * * * *
(ii) Make two composites of representative grab samples collected.
* * * * *
(B) Subsequent Verification Testing: Following written notification by
EPA, Tokusen may substitute the testing conditions in (3)(B) for (3)(A).
Tokusen must continue to monitor operating conditions, and analyze
representative samples each quarter of operation during the first year
of waste generation, using appropriate methods. As applicable to the
method-defined parameters of concern, analyses requiring the use of
SW–846 methods incorporated by reference in 40 CFR 260.11 must
be used without substitution. As applicable, the SW–846 methods
might include Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040,
0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312,
1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA
Method 1664, Rev. A), 9071B, and 9095B. The samples must represent the waste generated during the quarter.
(C) * * *
(i) * * *
(ii) Following cancellation of the quarterly testing, Tokusen must continue
to test a representative composite sample for all constituents listed in
Paragraph (1) annually (by twelve months after final exclusion), using
appropriate methods. As applicable to the method-defined parameters
of concern, analyses requiring the use of SW–846 methods incorporated by reference in 40 CFR 260.11 must be used without substitution. As applicable, the SW–846 methods might include Methods
0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061,
1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C,
9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev.
A), 9071B, and 9095B.
* * * * *
*
*
Tyco Printed Circuit Group, Melbourne Division.
*
Melbourne, Florida ......................
*
* *
*
*
*
*
*
*
(1) Verification Testing Requirements: Sample collection and analyses,
including quality control procedures must be performed using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CDFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. Methods must meet Performance Based Measurement System Criteria in which the Data Quality Objectives are to demonstrate that representative samples of the Tyco Sludge meet the
delisting levels in Condition (3).
* * * * *
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TABLE 1.—WASTES EXCLUDED FROM NON-SPECIFIC SOURCES—Continued
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*
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*
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*
20. Appendix IX to part 261 is
amended in Table 2:
I a. By removing the entry for ‘‘Bekaert
Corp., Dyersburg, TN’’;
I b. In the entry for ‘‘Bethlehem Steel
Corp., Steelton, PA,’’ under the ‘‘Waste
description’’ column, by revising
paragraphs (1) and (2);
I c. In the entry for ‘‘Bethlehem Steel
Corp., Johnston, PA,’’ under the ‘‘Waste
description’’ column, by revising
paragraphs (1) and (2);
I d. In the entry for ‘‘BF Goodrich
Intermediates Company, Inc., Calvert
City, Kentucky,’’ under the ‘‘Waste
description’’ column, by revising the
introductory paragraph and by revising
paragraphs (1)(B) and (3);
I e. In the entry for ‘‘CF&I Steel
Corporation, Pueblo, Colorado,’’ under
the ‘‘Waste description’’ column, by
revising paragraphs (1) and (2);
I f. In the entry for ‘‘Chaparral Steel
Midlothian L.P., Midlothian, Texas,’’
under the ‘‘Waste description’’ column,
by revising paragraph (1) and the
introductory text of paragraph (3);
I g. In the entry for ‘‘Conversion
Systems, Inc., Horsham, Pennsylvania,’’
under the ‘‘Waste description’’ column,
I
*
*
by revising the introductory text of
paragraph (1);
I h. In the entry for ‘‘DOE–RL, Richland,
Washington,’’ under the ‘‘Waste
description’’ column, by revising the
introductory text of paragraph (1) and by
revising paragraph (3);
I i. In the entry for ‘‘Envirite of
Pennsylvania (formerly Envirite
Corporation), York, Pennsylvania,’’
under the ‘‘Waste description’’ column,
by revising paragraph (2);
I j. In the entry for ‘‘Heritage
Environmental Services, LLC, at the
Nucor Steel Facility, Crawfordsville,
Indiana,’’ under the ‘‘Waste Description’’
column, by revising paragraph (2);
I k. In the entry for ‘‘Marathon Oil Co.,
Texas City, TX,’’ under the ‘‘Waste
description’’ column, by revising the
introductory text of paragraph (1);
I l. In the entry for ‘‘Occidental
Chemical Corp, Muscle Shoals Plant,
Sheffield, Alabama,’’ under the ‘‘Waste
description’’ column, by revising the
introductory paragraph and by revising
paragraphs (1)(A) and (3);
I m. In the entry for ‘‘Occidental
Chemical Corporation, Delaware City,
Delaware,’’ under the ‘‘Waste
*
*
description’’ column, by revising the
introductory paragraph and by revising
paragraph (1)(A), the introductory text of
paragraph (2) and by revising paragraph
(3);
I n. In the entry for ‘‘Oxy Vinyls, Deer
Park, Texas,’’ under the ‘‘Waste
description’’ column, by revising the
introductory text of paragraph (3);
I o. By adding the entry for ‘‘OxyVinyls,
L.P., Deer Park, TX,’’ after the entry for
‘‘Oxy Vinyls, Deer Park, Texas;’’
I p. In the entry for ‘‘Roanoke Electric
Steel Corp., Roanoke, VA,’’ under the
‘‘Waste description’’ column, by revising
paragraphs (1)(A), (1)(B), and (2);
I q. In the entry for ‘‘USX Steel
Corporation, USS Division, Southworks
Plant, Gary Works, Chicago, Illinois,’’
under the ‘‘Waste description’’ column,
by revising the introductory text of
paragraph (1) and by revising paragraphs
(1)(A) and (2).
The revisions read as follows:
Appendix IX to Part 261—Wastes
Excluded Under §§ 260.20 and 260.22
*
*
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*
TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES
Facility
Address
Waste description
*
*
Bethlehem Steel Corp .................
*
Steelton, PA ................................
*
*
*
*
* * * * *
(1) Testing:
(A) Initial Testing: During the first four weeks of operation of the full-scale
treatment system, Bethlehem must collect representative grab samples
of each treated batch of the CSEAFD and composite the grab samples
daily. The daily composites, prior to disposal, must be analyzed for the
EP leachate concentrations of all the EP toxic metals, nickel and cyanide (using distilled water in the cyanide extractions). Analyses must
be performed using appropriate methods. As applicable to the methoddefined parameters of concern, analyses requiring the use of SW–846
methods incorporated by reference in 40 CFR 260.11 must be used
without substitution. As applicable, the SW–846 methods might include
Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051,
0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A,
9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method
1664, Rev. A), 9071B, and 9095B. Bethlehem must report the analytical test data obtained during this initial period no later than 90 days
after the treatment of the first full-scale batch.
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TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES—Continued
Facility
Address
Bethlehem Steel Corp .................
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(B) Subsequent Testing: Bethlehem must collect representative grab
samples from every treated batch of CSEAFD generated daily and
composite all of the grab samples to produce a weekly composite sample. Bethlehem then must analyze each weekly composite sample for
the EP leachate concentrations of all the EP toxic metals and nickel.
Analyses must be performed using appropriate methods. As applicable
to the method-defined parameters of concern, analyses requiring the
use of SW–846 methods incorporated by reference in 40 CFR 260.11
must be used without substitution. As applicable, the SW–846 methods
might include Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040,
0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312,
1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA
Method 1664, Rev. A), 9071B, and 9095B. The analytical data, including all quality control information, must be compiled and maintained on
site for a minimum of three years. These data must be furnished upon
request and made available for inspection by any employee or representative of EPA or the State of Pennsylvania.
(2) Delisting Levels: If the EP extract concentrations resulting from the
testing in condition (1)(A) or (1)(B) for chromium, lead, arsenic, or silver exceeds 0.315 mg/l; for barium exceeds 6.3 mg/l; for cadmium or
selenium exceed 0.063 mg/l; for mercury exceeds 0.0126 mg/l; for
nickel exceeds 3.15 mg/l; or for cyanide exceeds 4.42 mg/l, the waste
must either be re-treated or managed and disposed in accordance with
subtitle C of RCRA.
* * * * *
(1) Testing:
(A) Initial Testing: During the first four weeks of operation of the full-scale
treatment system, Bethlehem must collect representative grab samples
of each treated batch of the CSEAFD and composite the grab samples
daily. The daily composites, prior to disposal, must be analyzed for the
EP leachate concentrations of all the EP toxic metals, nickel, and cyanide (using distilled water in the cyanide extractions). Analyses must
be performed using appropriate methods. As applicable to the methoddefined parameters of concern, analyses requiring the use of SW–846
methods incorporated by reference in 40 CFR 260.11 must be used
without substitution. As applicable, the SW–846 methods might include
Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051,
0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A,
9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method
1664, Rev. A), 9071B, and 9095B. Bethlehem must report the analytical test data obtained during this initial period no later than 90 days
after the treatment of the first full-scale batch.
(B) Subsequent Testing: Bethlehem must collect representative grab
samples from every treated batch of CSEAFD generated daily and
composite all of the grab samples to produce a weekly composite sample. Bethlehem then must analyze each weekly composite sample for
the EP leachate concentrations of all the EP toxic metals and nickel.
Analyses must be performed using appropriate methods. As applicable
to the method-defined parameters of concern, analyses requiring the
use of SW–846 methods incorporated by reference in 40 CFR 260.11
must be used without substitution. As applicable, the SW–846 methods
might include Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040,
0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312,
1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA
Method 1664, Rev. A), 9071B, and 9095B. The analytical data, including all quality control information, must be compiled and maintained on
site for a minimum of three years. These data must be furnished upon
request and made available for inspection by any employee or representative of EPA or the State of Pennsylvania.
(2) Delisting Levels: If the EP extract concentrations resulting from the
testing in condition (1)(A) or (1)(B) for chromium, lead, arsenic, or silver exceed 0.315 mg/l; for barium exceeds 6.3 mg/l; for cadmium or
selenium exceed 0.063 mg/l; for mercury exceeds 0.0126 mg/l; for
nickel exceeds 3.15 mg/l; or for cyanide exceeds 4.42 mg/l, the waste
must either be retreated until it meets these levels or managed and
disposed in accordance with subtitle C of RCRA.
* * * * *
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TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES—Continued
Facility
Address
Waste description
BF Goodrich Intermediates Company, Inc.
Calvert City, Kentucky .................
CF&I Steel Corporation ...............
Pueblo, Colorado ........................
Brine purification muds and saturator insolubles (EPA Hazardous Waste
No. K071) after August 18, 1989. This exclusion is conditional upon
the collection and submission of data obtained from BFG’s full-scale
treatment system because BFG’s original data was based on data presented by another petitioner using an identical treatment process. To
ensure that hazardous constituents are not present in the waste at levels of regulatory concern once the full-scale treatment facility is in operation, BFG must implement a testing program. All sampling and analyses (including quality control procedures) must be performed using
appropriate methods. As applicable to the method-defined parameters
of concern, analyses requiring the use of SW–846 methods incorporated by reference in 40 CFR 260.11 must be used without substitution. As applicable, the SW–846 methods might include Methods
0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061,
1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C,
9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev.
A), 9071B, and 9095B. This testing program must meet the following
conditions for the exclusion to be valid:
(1) * * *
(B) Collect representative grab samples from every batch of treated mercury brine purification muds and treated saturator insolubles on a daily
basis and composite the grab samples to produce two separate weekly
composite samples (one of the treated mercury brine muds and one of
the treated saturator insolubles). Prior to disposal of the treated
batches, two weekly composite samples must be analyzed for the EP
leachate concentrations of all the EP toxic metals (except mercury),
nickel, and cyanide (using distilled water in the cyanide extractions).
BFG must report the analytical test data, including all quality control
data, obtained during this initial period no later than 90 days after the
treatment of the first full-scale batch.
(2) * * *
(3) If, under condition (1) or (2), the EP leachate concentrations for chromium, lead, arsenic, or silver exceed 0.316 mg/l; for barium exceeds
6.31 mg/l; for cadmium or selenium exceed 0.063 mg/l; for mercury exceeds 0.0126 mg/l, for nickel exceeds 3.16 mg/l; or for cyanide exceeds 4.42 mg/l, the waste must either be retreated until it meets
these levels or managed and disposed of in accordance with subtitle C
of RCRA.
* * * * *
* * * * *
(1) Testing:
(A) Initial Testing: During the first four weeks of operation of the full-scale
treatment system, CF&I must collect representative grab samples of
each treated batch of the CSEAFD and composite the grab samples
daily. The daily composites, prior to disposal, must be analyzed for the
EP leachate concentrations of all the EP toxic metals, nickel, and cyanide (using distilled water in the cyanide extractions). Analyses must
be performed using appropriate methods. As applicable to the methoddefined parameters of concern, analyses requiring the use of SW–846
methods incorporated by reference in 40 CFR 260.11 must be used
without substitution. As applicable, the SW–846 methods might include
Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051,
0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A,
9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method
1664, Rev. A), 9071B, and 9095B. CF&I must report the analytical test
data obtained during this initial period no later than 90 days after the
treatment of the first full-scale batch.
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TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES—Continued
Facility
Address
Waste description
Chaparral Steel Midlothian, L.P.
Midlothian, Texas ........................
Conversion Systems, Inc. ...........
Horsham, Pennsylvania ..............
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(B) Subsequent Testing: CF&I must collect representative grab samples
from every treated batch of CSEAFD generated daily and composite all
of the grab samples to produce a weekly composite sample. CF&I then
must analyze each weekly composite sample for the EP leachate concentrations of all of the EP toxic metals and nickel. Analyses must be
performed using appropriate methods. As applicable to the method-defined parameters of concern, analyses requiring the use of SW–846
methods incorporated by reference in 40 CFR 260.11 must be used
without substitution. As applicable, the SW–846 methods might include
Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051,
0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A,
9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method
1664, Rev. A), 9071B, and 9095B. The analytical data, including all
quality control information, must be compiled and maintained on site
for a minimum of three years. These data must be furnished upon request and made available for inspection by any employee or representative of EPA or the State of Colorado.
(2) Delisting levels: If the EP extract concentrations determined in conditions (1)(A) or (1)(B) for chromium, lead, arsenic, or silver exceed
0.315 mg/l; for barium exceeds 6.3 mg/l; for cadmium or selenium exceed 0.063 mg/l; for mercury exceeds 0.0126 mg/l; for nickel exceeds
3.15 mg/l; or for cyanide exceeds 4.42 mg/l, the waste must either be
re-treated or managed and disposed in accordance with Subtitle C of
RCRA.
* * * * *
(1) Delisting Levels: All concentrations for the constituent total lead in the
approximately 2,500 cubic yards (500,000 gallons) per calender year of
raw leachate from Landfill No. 3, storm water from the baghouse area,
and other K061 wastewaters that is transferred from the storage tank
to nonhazardous management must not exceed 0.69 mg/l (ppm). Constituents must be measured in the waste by appropriate methods. As
applicable to the method-defined parameters of concern, analyses requiring the use of SW–846 methods incorporated by reference in 40
CFR 260.11 must be used without substitution. As applicable, the SW–
846 methods might include Methods 0010, 0011, 0020, 0023A, 0030,
0031, 0040, 0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B,
1311, 1312, 1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A,
9070A (uses EPA Method 1664, Rev. A), 9071B, and 9095B.
* * * * *
(3) Verification Testing Requirements: Sample collection and analyses,
including quality control procedures, must be performed using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. Chaparral Steel must analyze one composite sample from each batch of untreated wastewater transferred from the hazardous waste storage tank to non-hazardous waste management.
Each composited batch sample must be analyzed, prior to non-hazardous management of the waste in the batch represented by that
sample, for the constituent lead as listed in Condition (1). Chaparral
may treat the waste as specified in Condition (2). If EPA judges the
treatment process to be effective during the operating conditions used
during the initial verification testing, Chaparral Steel may replace the
testing requirement in Condition (3)(A) with the testing requirement in
Condition (3)(B). Chaparral must continue to test as specified in (3)(A)
until and unless notified by EPA or designated authority that testing in
Condition (3)(A) may be replaced by Condition (3)(B).
* * * * *
* * * * *
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TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES—Continued
Facility
Address
Waste description
DOE–RL ......................................
Richland, Washington .................
*
*
Envirite of Pennsylvania (formerly
Envirite Corporation).
*
York, Pennsylvania .....................
(1) Verification Testing Requirements: Sample collection and analyses,
including quality control procedures, must be performed using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B.
* * * * *
* * * * *
(1) Testing: Sample collection and analyses (including quality control
(QC) procedures) must be performed using appropriate methods. As
applicable to the method-defined parameters of concern, analyses requiring the use of SW–846 methods incorporated by reference in 40
CFR 260.11 must be used without substitution. As applicable, the SW–
846 methods might include Methods 0010, 0011, 0020, 0023A, 0030,
0031, 0040, 0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B,
1311, 1312, 1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A,
9070A (uses EPA Method 1664, Rev. A), 9071B, and 9095B. If EPA
judges the treatment process to be effective under the operating conditions used during the initial verification testing, DOE may replace the
testing required in Condition (1)(A) with the testing required in Condition (1)(B). DOE must continue to test as specified in Condition (1)(A)
until notified by EPA in writing that testing in Condition (1)(A) may be
replaced by Condition (1)(B).
* * * * *
(2) * * *
(3) Delisting Levels: All total constituent concentrations in the waste samples must be measured using appropriate methods. As applicable to
the method-defined parameters of concern, analyses requiring the use
of SW–846 methods incorporated by reference in 40 CFR 260.11 must
be used without substitution. As applicable, the SW–846 methods
might include Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040,
0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312,
1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA
Method 1664, Rev. A), 9071B, and 9095B. All total constituent concentrations must be equal to or less than the following levels (ppm):
Inorganic Constituents, Ammonium—10.0, Antimony—0.06, Arsenic—0.5,
Barium—20.0, Beryllium—0.04, Cadmium—0.05, Chromium—1.0, Cyanide—2.0, Fluoride—40.0, Lead—0.15, Mercury—0.02, Nickel—1.0,
Selenium—0.5, Silver—2.0, Vanadium—2.0, Zinc—100.0, Organic
Constituents, Acetone—40.0, Benzene—0.05, Benzyl alcohol—100.0,
1-Butyl alcohol—40.0, Carbon tetrachloride—0.05, Chlorobenzene—
1.0, Chloroform—0.1, Cresol—20.0, 1,4-Dichlorobenzene—0.75, 1,2Dichloroethane—0.05, 1,1-Dichloroethylene—0.07, Di-n-octyl phthalate—7.0, Hexachloroethane—0.06, Methyl ethyl ketone—200.0, Methyl
isobutyl ketone—30.0, Naphthalene—10.0, Tetrachloroethylene—0.05,
Toluene—10.0, Tributyl phosphate—0.2, 1,1,1-Trichloroethane—2.0,
1,1,2-Trichloroethane—0.05, Trichloroethylene—0.05, Vinyl Chloride—
0.02.
* * * * *
*
* *
*
*
*
*
*
*
(2) Each batch of treatment residue (formerly must be tested for leachable cyanide. If the leachable cyanide levels Corporation) (using the
EP Toxicity test without acetic acid adjustment) exceed 1.26 ppm, the
waste must be re-treated or managed and disposed as a hazardous
waste under 40 CFR Parts 262 to 265 and the permitting standards of
40 CFR Part 270.
* * * * *
*
*
Heritage Environmental Services,
LLC, at the Nucor Steel facility.
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Crawfordsville, Indiana ................
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* *
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*
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Facility
Address
Waste description
(2) Verification Testing: On a monthly basis, Heritage or Nucor must analyze two samples of the waste using the TCLP, SW–846 Method 1311,
with an extraction fluid of pH 12 ± 0.05 standard units and for the mercury determinative analysis of the leachate using an appropriate method. The constituent concentrations measured must be less than the
delisting levels established in Paragraph (1).
* * * * *
*
*
Marathon Oil Co ..........................
*
Texas City, TX ............................
*
*
*
*
* * * * *
(1) Testing: Sample collection and analyses (including quality control
(QC) procedures) must be performed using appropriate methods. As
applicable to the method-defined parameters of concern, analyses requiring the use of SW–846 methods incorporated by reference in 40
CFR 260.11 must be used without substitution. As applicable, the SW–
846 methods might include Methods 0010, 0011, 0020, 0023A, 0030,
0031, 0040, 0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B,
1311, 1312, 1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A,
9070A (uses EPA Method 1664, Rev. A), 9071B, and 9095B. If EPA
judges the treatment process to be effective under the operating conditions used during the initial verification testing, Marathon may replace
the testing required in Condition (1)(A) with the testing required in Condition (1)(B). Marathon must continue to test as specified in Condition
(1)(A), including testing for organics in Conditions (3)(B) and (3)(C),
until and unless notified by EPA in writing that testing in Condition
(1)(A) may be replaced by Condition (1)(B), or that testing for organics
may be terminated as described in (1)(C) (to the extent directed by
EPA).
* * * * *
*
*
Occidental Chemical Corp., Muscle Shoals Plant.
*
Sheffield, Alabama ......................
*
*
*
*
Retorted wastewater treatment sludge from the mercury cell process in
chlorine production (EPA Hazardous Plant Waste No. K106) after September 19, 1989. This exclusion is conditional upon the submission of
data obtained from Occidental’s full-scale retort treatment system because Occidental’s original data were based on a pilot-scale retort system. To ensure that hazardous constituents are not present in the
waste at levels of regulatory concern once the full-scale treatment facility is in operation, Occidental must implement a testing program. All
sampling and analyses (including quality control procedures) must be
performed using appropriate methods. As applicable to the method-defined parameters of concern, analyses requiring the use of SW–846
methods incorporated by reference in 40 CFR 260.11 must be used
without substitution. As applicable, the SW–846 methods might include
Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051,
0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A,
9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method
1664, Rev. A), 9071B, and 9095B. This testing program must meet the
following conditions for the exclusion to be valid:
(1) * * *
(A) Collect representative grab samples from every batch of retorted material and composite the grab samples to produce a weekly composite
sample. The weekly composite samples, prior to disposal or recycling,
must be analyzed for the EP leachate concentrations of all the EP
toxic metals (except mercury), nickel, and cyanide (using distilled water
in the cyanide extractions). Occidental must report the analytical test
data, including all quality control data, obtained during this initial period
no later than 90 days after the treatment of the first full-scale batch.
* * * * *
(2) * * *
(3) If, under condition (1) or (2), the EP leachate concentrations for chromium, lead, arsenic, or silver exceed 1.616 mg/l; for barium exceeds
32.3 mg/l; for cadmium or selenium exceed 0.323 mg/l; for mercury exceeds 0.065 mg/l, for nickel exceeds 16.15 mg/l; or for cyanide exceeds 22.61 mg/l, the waste must either be retreated until it meets
these levels or managed and disposed of in accordance with subtitle C
of RCRA.
* * * * *
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TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES—Continued
Facility
Address
Waste description
Occidental Chemical Corporation
Delaware City, Delaware ............
Sodium chloride treatment muds (NaCl-TM), sodium chloride saturator
cleanings (NaCl-SC), and potassium chloride treatment muds (KCl-TM)
(all classified as EPA Hazardous Waste No. K071) generated at a
maximum combined rate (for all three wastes) of 1,018 tons per year.
This exclusion was published on April 29, 1991 and is conditioned
upon the collection of data from Occidental’s full-scale brine treatment
system because Occidental’s request for exclusion was based on data
from a laboratory-scale brine treatment process. To ensure that hazardous constituents are not present in the waste at levels of regulatory
concern once the full-scale treatment system is in operation, Occidental must implement a testing program for the petitioned waste. All
sampling and analyses (including quality control (QC) procedures)
must be performed using appropriate methods. As applicable to the
method-defined parameters of concern, analyses requiring the use of
SW–846 methods incorporated by reference in 40 CFR 260.11 must
be used without substitution. As applicable, the SW–846 methods
might include Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040,
0050, 0051, 0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312,
1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA
Method 1664, Rev. A), 9071B, and 9095B. This testing program must
meet the following conditions for the exclusion to be valid:
(1) * * *
(A) Collect representative grab samples from each batch of the three
treated wastestreams (sodium chloride saturator cleanings (NaCl-SC),
sodium chloride treatment muds (NaCl-TM) and potassium chloride
treatment muds (KCl-TM)) on an as generated basis and composite
the samples to produce three separate weekly composite samples (of
each type of K071 waste). The three weekly composite samples, prior
to disposal, must be analyzed for the EP leachate concentrations of all
the EP toxic metals (except mercury), nickel, and cyanide (using distilled water in the cyanide extractions). Occidental must report the
waste volumes produced and the analytical test data, including all
quality control data, obtained during this initial period, no later than 90
days after the treatment of the first full-scale batch. * * *
(2) Subsequent Testing: After the first four weeks of full-scale treatment
operations, Occidental must do the following; all sampling and analyses (including quality control procedures) must be performed using
appropriate methods, and as applicable to the method-defined parameters of concern, analyses requiring the use of SW–846 methods incorporated by reference in 40 CFR 260.11 must be used without substitution. As applicable, the SW–846 methods might include Methods
0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061,
1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C,
9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev.
A), 9071B, and 9095B: * * *
(3) If, under conditions (1) or (2), the EP leachate concentrations for
chromium, lead, arsenic, or silver exceed 0.77 mg/l; for barium exceeds 15.5 mg/l; for cadmium or selenium exceed 0.16 mg/l; for mercury exceeds 0.031 mg/l, or for nickel or total cyanide exceed 10.9 mg/
l, the waste must either be retreated or managed and disposed of in
accordance with all applicable hazardous waste regulations.
* * * * *
*
*
OxyVinyls .....................................
*
Deer Park, Texas ........................
*
*
*
*
* * * * *
(3) Verification Testing Requirements: Sample collection and analyses,
including quality control procedures, must be performed using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. If EPA judges the incineration process to be effective under the operating conditions used during the initial verification
testing, OxyVinyls may replace the testing required in Condition (3)(A)
with the testing required in Condition (3)(B). OxyVinyls must continue
to test as specified in Condition (3)(A) until and unless notified by EPA
in writing that testing in Condition (3)(A) may be replaced by Condition
(3)(B).
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TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES—Continued
Facility
Address
OxyVinyls, L.P. ............................
Deer Park, TX .............................
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* * * * *
Incinerator Offgas Scrubber Water (EPA Hazardous Waste Nos. K017,
K019 and K020) generated at a maximum annual rate of 919,990
cubic yards per calendar year after April 22, 2004, and disposed in accordance with the TPDES permit. For the exclusion to be valid,
OxyVinyls must implement a testing program that meets the following
Paragraphs:
(1) Delisting Levels: All total concentrations for those constituents must
not exceed the following levels (mg/kg) in the incinerator offgas scrubber water. Incinerator offgas treatment scrubber water (i) Inorganic
Constituents Antimony—0.0204; Arsenic—0.385; Barium—2.92; Beryllium—0.166; Cadmium—0.0225; Chromium—5.0; Cobalt—13.14; Copper—418.00; Lead—5.0; Nickel—1.13; Mercury—0.0111; Vanadium—
0.838; Zinc—2.61 (ii) Organic Constituents Acetone—1.46;
Bromoform—0.481; Bromomethane—8.2; Bromodichloromethane—
0.0719;
Chloroform—0.683;
Dibromochloromethane—0.057;
Iodomethane—0.19; Methylene Chloride—0.029; 2,3,7,8—TCDD
equivalents as TEQ—0.0000926
(2) Waste Management: (A) OxyVinyls must manage as hazardous all incinerator offgas treatment scrubber water generated, until it has completed initial verification testing described in Paragraphs (3)(A) and (B),
as appropriate, and valid analyses show that paragraph (1) is satisfied.
(B) Levels of constituents measured in the samples of the incinerator
offgas treatment scrubber water that do not exceed the levels set forth
in Paragraph (1) are non-hazardous. OxyVinyls can manage and dispose the non-hazardous incinerator offgas treatment scrubber water
according to all applicable solid waste regulations.
(C) If constituent levels in a sample exceed any of the delisting levels set
in Paragraph (1), OxyVinyls must collect one additional sample and
perform the expedited analyses to confirm if the constituent exceeds
the delisting level. If this sample confirms the exceedance, OxyVinyls
must, from that point forward, treat the waste as hazardous until it is
demonstrated that the waste again meets the levels set in Paragraph
(1). OxyVinyls must notify EPA of the exceedance and resampling analytical results prior to disposing of the waste.
(D) If the waste exceeds the levels in paragraph (1) OxyVinyls must
manage and dispose of the waste generated under Subtitle C of RCRA
from the time that it becomes aware of any exceedance.
(E) Upon completion of the Verification Testing described in Paragraphs
3(A) and (B) as appropriate and the transmittal of the results to EPA,
and if the testing results meet the requirements of Paragraph (1),
OxyVinyls may proceed to manage its incinerator offgas treatment
scrubber water as non-hazardous waste. If subsequent verification
testing indicates an exceedance of the Delisting Levels in Paragraph
(1), OxyVinyls must manage the incinerator offgas treatment scrubber
water as a hazardous waste until two consecutive quarterly testing
samples show levels below the Delisting Levels.
(3) Verification Testing Requirements: OxyVinyls must perform sample
collection and analyses, including quality control procedures, using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051, 0060, 0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. If EPA judges the process to be effective under the
operating conditions used during the initial verification testing,
OxyVinlys may replace the testing required in Paragraph (3)(A) with
the testing required in Paragraph (3)(B). OxyVinyls must continue to
test as specified in Paragraph (3)(A) until and unless notified by EPA
in writing that testing in Paragraph (3)(A) may be replaced by Paragraph (3)(B).
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TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES—Continued
Facility
Address
Waste description
(A) Initial Verification Testing: After EPA grants the final exclusion,
OxyVinyls must do the following: (i) Within 60 days of this exclusion
becoming final, collect four samples, before disposal, of the incinerator
offgas treatment scrubber water. (ii) The samples are to be analyzed
and compared against the delisting levels in Paragraph (1) (iii). Within
sixty (60) days after the exclusion becomes final, OxyVinyls will report
initial verification analytical test data, including analytical quality control
information for the first sixty (30) days of operation after this exclusion
becomes final of the incinerator offgas treatment scrubber water. If levels of constituents measured in the samples of the incinerator offgas
treatment scrubber water that do not exceed the levels set forth in
Paragraph (1) and are also non-hazardous in two consecutive quarters
after the first thirty (30) days of operation after this exclusion,
OxyVinyls can manage and dispose of the incinerator offgas treatment
scrubber water according to all applicable solid water regulations after
reporting the analytical results to EPA.
(B) Subsequent Verification Testing: Following written notification by
EPA, OxyVinyls may substitute the testing conditions in Paragraph
(3)(B) for (3)(A). OxyVinyls must continue to monitor operating conditions, and analyze representative samples of each quarter of operation
during the first year of waste generation. The samples must represent
the waste generated during the quarter. After the first year of analytical
sampling verification sampling can be performed on a single annual
composite sample of the incinerator offgas treatment scrubber water.
The results are to be compared to the delisting levels in Condition (1).
(C) Termination of Testing: (i) After the first year of quarterly testing, if
the Delisting Levels in Paragraph (1) are being met, OxyVinyls may
then request that EPA stop requiring quarterly testing. After EPA notifies OxyVinyls in writing, the company may end quarterly testing. (ii)
Following cancellation of the quarterly testing, OxyVinyls must continue
to test a representative sample for all constituents listed in Paragraph
(1) annually.
(4) Changes in Operating Conditions: If OxyVinyls significantly changes
the process described in its petition or starts any processes that generate(s) the waste that may or could significantly affect the composition
or type of waste generated as established under Paragraph (1) (by illustration, but not limitation, changes in equipment or operating conditions of the treatment process), it must notify EPA in writing; OxyVinyls
may no longer handle the wastes generated from the new process as
nonhazardous until the wastes meet the delisting levels set in Paragraph (1) and it has received written approval to do so from EPA.
(5) Data Submittals: OxyVinyls must submit the information described
below. If OxyVinyls fails to submit the required data within the specified
time or maintain the required records on-site for the specified time,
EPA, at its discretion, will consider this sufficient basis to reopen the
exclusion as described in Paragraph 6. OxyVinyls must:
(A) Submit the data obtained through Paragraph 3 to the Section Chief,
EPA Region 6 Corrective Action and Waste Minimization Section, 1445
Ross Avenue, Dallas, Texas 75202–2733, Mail Code, (6PD–C) within
the time specified.
(B) Compile records of operating conditions and analytical data from
Paragraph (3), summarized, and maintained on-site for a minimum of
five years.
(C) Finish these records and data when EPA or the State of Texas request them for inspection.
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TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES—Continued
Facility
Address
Waste description
(D) Send along with all data a signed copy of the following certification
statement, to attest to the truth and accuracy of the data submitted:
Under civil and criminal penalty of law for the making or submission of
false or fraudulent statements or representations (pursuant to the applicable provisions of the Federal Code, which include, but may not be
limited to, 18 U.S.C. 1001 and 42 U.S.C. 6928), I certify that the information contained in or accompanying this document is true, accurate
and complete. As to the (those) identified section(s) of this document
for which I cannot personally verify its (their) truth and accuracy, I certify as the company official having supervisory responsibility for the
persons who, acting under my direct instructions, made the verification
that this information is true, accurate and complete. If any of this information is determined by EPA in its sole discretion to be false, inaccurate or incomplete, and upon conveyance of this fact to the company, I recognize and agree that this exclusion of waste will be void as
if its never had effect or to the extent directed by EPA and that the
company will be liable for any actions taken in contravention of the
company’s RCRA and CERCLA obligations premised upon the company’s reliance on the void exclusion.
(6) Reopener: (A) If, anytime after disposal of the delisted waste
OxyVinyls possesses or is otherwise made aware of any environmental
data (including but not limited to leachate data or groundwater monitoring data) or any other data relevant to the delisted waste indicating
that any constituent identified for the delisting verification testing is at a
level higher than the delisting level allowed by the Regional Administrator or his delegate in granting the petition, then the facility must report the data, in writing, to the Regional Administrator or his delegate
within 10 days of first possessing or being made aware of that data.
(B) If the annual testing of the waste does not meet the delisting requirements in Paragraph 1, OxyVinyls must report the data, in writing, to the
Regional Administrator or his delegate within 10 days of first possessing or being made aware of that data.
(C) If OxyVinyls fails to submit the information described in paragraphs
(5), (6)(A) or (6)(B) or if any other information is received from any
source, the Regional Administrator or his delegate will make a preliminary determination as to whether the reported information requires
EPA action to protect human health or the environment. Further action
may include suspending, or revoking the exclusion, or other appropriate response necessary to protect human health and environment.
(D) If the Regional Administrator or his delegate determines that the reported information does require action by EPA’s Regional Administrator
or his delegate will notify the facility in writing of the actions the Regional Administrator or his delegate believes are necessary to protect
human health and the environment. The notice shall include a statement of the proposed action and a statement providing the facility with
an opportunity to present information as to why the proposed EPA action is not necessary. The facility shall have 10 days from the date of
the Regional Administrator or his delegate’s notice to present such information.
(E) Following the receipt of information from the facility described in paragraph (6)(D) or (of no information is presented under paragraph (6)(D))
the initial receipt of information described in paragraphs (5), (6)(A) or
(6)(B), the Regional Administrator or his delegate will issue a final written determination describing EPA actions that are necessary to protect
human health or the environment. Any require action described in the
Regional Administrator or his delegate’s determination shall become
effective immediately, unless the Regional Administrator or his delegate provides otherwise.
(7) Notification Requirements: OxyVinyls must do the following before
transporting the delisted waste. Failure to provide this notification will
result in a violation of the delisting petition and a possible revocation of
the decision.
(A) Provide a one-time written notification to any State Regulatory Agency to which or through which it will transport the delisted waste described above for disposal, 60 days before beginning such activities.
(B) Update the one-time written notification if it ships the delisted waste
into a different disposal facility.
(C) Failure to provide this notification will result in a violation of the
delisting variance and a possible revocation of the decision.
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TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES—Continued
Facility
Address
Waste description
*
*
Roanoke Electric Steel Corp .......
*
Roanoke, VA ...............................
*
*
*
*
* * * * *
(1) * * *
(A) Initial Testing: During the first four weeks of operation of the full-scale
treatment system, Roanoke must collect representative grab samples
of each treated batch of the CSEAFD and composite the grab samples
daily. The daily composites, prior to disposal, must be analyzed for the
EP leachate concentrations of all the EP toxic metals, nickel and cyanide (using distilled water in the cyanide extractions). Analyses must
be performed using appropriate methods. As applicable to the methoddefined parameters of concern, analyses requiring the use of SW–846
methods incorporated by reference in 40 CFR 260.11 must be used
without substitution. As applicable, the SW–846 methods might include
Methods 0010, 0011, 0020, 0023A, 0030, 0031, 0040, 0050, 0051,
0060, 0061, 1010A, 1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A,
9010C, 9012B, 9040C, 9045D, 9060A, 9070A (uses EPA Method
1664, Rev. A), 9071B, and 9095B. Roanoke must report the analytical
test data obtained during this initial period no later than 90 days after
the treatment of the first full-scale batch.
(B) Subsequent Testing: Roanoke must collect representative grab samples from every treated batch of CSEAFD generated daily and composite all of the grab samples to produce a weekly composite sample.
Roanoke then must analyze each weekly composite sample for all of
the EP toxic metals and nickel. Analyses must be performed using appropriate methods. As applicable to the method-defined parameters of
concern, analyses requiring the use of SW–846 methods incorporated
by reference in 40 CFR 260.11 must be used without substitution. As
applicable, the SW–846 methods might include Methods 0010, 0011,
0020, 0023A, 0030, 0031, 0040, 0050, 0051,0060,0061, 1010A,
1020B, 1110A, 1310B, 1311, 1312, 1320, 1330A, 9010C, 9012B,
9040C, 9045D, 9060A, 9070A (uses EPA Method 1664, Rev. A),
9071B, and 9095B. The analytical data, including all quality control information, must be compiled and maintained on site for a minimum of
three years. These data must be furnished upon request and made
available for inspection for any employee or representative of EPA or
the State of Virginia.
(2) Delistiing levels: If the EP extract concentrations for chromium, lead,
arsenic, or silver exceed 0.315 mg/l; for barium exceeds 6.3 mg/l; for
cadmium or selenium exceed 0.063 mg/l; for mercury exceeds 0.0126
mg/l, for nickel exceeds 3.15 mg/l, or for cyanide exceeds 1.26 mg/l,
the waste must either be re-treated or managed and disposed in accordance with subtitle C of RCRA.
* * * * *
*
*
USX Steel Corporation, USS Division, Southworks Plant, Gary
Works.
*
Chicago, Illinois ...........................
*
*
*
*
(1) Testing: Sample collection and analyses (including quality control
(QC) procedures) must be performed using appropriate methods. As
applicable to the method-defined parameters of concern, analyses requiring the use of SW–846 methods incorporated by reference in 40
CFR 260.11 must be used without substitution. As applicable, the SW–
846 methods might include Methods 0010, 0011, 0020, 0023A, 0030,
0031, 0040, 0050, 0051, 0060, 0061,1010A, 1020B, 1110A, 1310B,
1311, 1312, 1320, 1330A, 9010C, 9012B, 9040C, 9045D, 9060A,
9070A (uses EPA Method 1664, Rev. A), 9071B, and 9095B.
(A) Initial Testing: During the first four weeks of operation of the full-scale
treatment system, USX must collect representative grab samples of
each treated batch of the CSEAFD and composite the grab samples
daily. The daily composites, prior to disposal, must be analyzed for the
EP leachate concentrations of all the EP toxic metals, nickel, and cyanide (using distilled water in the cyanide extractions). USX must report
the analytical test data, including quality control information, obtained
during this initial period no later than 90 days after the treatment of the
first full-scale batch. * * *
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TABLE 2.—WASTES EXCLUDED FROM SPECIFIC SOURCES—Continued
Facility
Address
Waste description
(2) Delisting levels: If the EP extract concentrations for chromium, lead,
arsenic, or silver exceed 0.315 mg/l; for barium exceeds 6.3 mg/l; for
cadmium or selenium exceed 0.063 mg/l; for mercury exceeds 0.0126
mg/l; for nickel exceeds 3.15 mg/l; or for cyanide exceeds 4.42 mg/l,
the waste must either be re-treated until it meets these levels or managed and disposed in accordance with subtitle C of RCRA.
*
*
*
*
*
*
*
Appendix IX to Part 261
[Amended]
21. Appendix IX to part 261 is
amended in Table 3 by removing the
entry for ‘‘Bekaert Corp., Dyersburg,
TN’’.
I
22. The authority citation for part 264
continues to read as follows:
I
Authority: 42 U.S.C. 6905, 6912(a), 6924,
6925, 6927, 6928(h), and 6974.
Subpart J—Tank Systems
23. Section 264.190 is amended by
revising paragraph (a) to read as follows:
I
Applicability.
*
*
*
*
*
(a) Tank systems that are used to store
or treat hazardous waste which contains
no free liquids and are situated inside
a building with an impermeable floor
are exempted from the requirements in
§ 264.193. To demonstrate the absence
or presence of free liquids in the stored/
treated waste, the following test must be
used: Method 9095B (Paint Filter
Liquids Test) as described in ‘‘Test
Methods for Evaluating Solid Waste,
Physical/Chemical Methods,’’ EPA
Publication SW–846, as incorporated by
reference in § 260.11 of this chapter.
*
*
*
*
*
Subpart N—Landfills
24. Section 264.314 is amended by
revising paragraph (c) to read as follows:
I
§ 264.314 Special requirements for bulk
and containerized liquids.
*
*
*
*
*
(c) To demonstrate the absence or
presence of free liquids in either a
containerized or a bulk waste, the
following test must be used: Method
9095B (Paint Filter Liquids Test) as
described in ‘‘Test Methods for
Evaluating Solid Waste, Physical/
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Chemical Methods,’’ EPA Publication
SW–846, as incorporated by reference in
§ 260.11 of this chapter.
*
*
*
*
*
Subpart AA—Air Emission Standards
for Process Vents
PART 264—STANDARDS FOR
OWNERS AND OPERATORS OF
HAZARDOUS WASTE TREATMENT,
STORAGE, AND DISPOSAL
FACILITIES
§ 264.190
*
25. Section 264.1034 is amended by
revising paragraphs (c)(1)(ii), (c)(1)(iv),
(d)(1)(iii) and (f) to read as follows:
I
§ 264.1034
Test methods and procedures.
*
*
*
*
*
(c) * * *
(1) * * *
(ii) Method 18 or Method 25A in 40
CFR part 60, appendix A, for organic
content. If Method 25A is used, the
organic HAP used as the calibration gas
must be the single organic HAP
representing the largest percent by
volume of the emissions. The use of
Method 25A is acceptable if the
response from the high-level calibration
gas is at least 20 times the standard
deviation of the response from the zero
calibration gas when the instrument is
zeroed on the most sensitive scale.
*
*
*
*
*
(iv) Total organic mass flow rates
shall be determined by the following
equation:
(A) For sources utilizing Method 18.
n
E h = Q 2sd ∑ C i MWi [0.0416] 10 −6
i =1
[
]
Where:
Eh = Total organic mass flow rate, kg/h;
Q2sd = Volumetric flow rate of gases
entering or exiting control device,
as determined by Method 2, dscm/
h;
n = Number of organic compounds in
the vent gas;
Ci = Organic concentration in ppm, dry
basis, of compound i in the vent
gas, as determined by Method 18;
MWi = Molecular weight of organic
compound i in the vent gas, kg/kgmol;
0.0416 = Conversion factor for molar
volume, kg-mol/m3 (@ 293 K and
760 mm Hg);
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*
*
10¥6 = Conversion from ppm
(B) For sources utilizing Method 25A.
Eh = (Q)(C)(MW)(0.0416)(10¥6)
Where:
Eh = Total organic mass flow rate, kg/h;
Q = Volumetric flow rate of gases
entering or exiting control device,
as determined by Method 2, dscm/
h;
C = Organic concentration in ppm, dry
basis, as determined by Method
25A;
MW = Molecular weight of propane, 44;
0.0416 = Conversion factor for molar
volume, kg-mol/m3 (@ 293 K and
760 mm Hg);
10¥6 = Conversion from ppm.
*
*
*
*
*
(d) * * *
(1) * * *
(iii) Each sample shall be analyzed
and the total organic concentration of
the sample shall be computed using
Method 9060A (incorporated by
reference under 40 CFR 260.11) of ‘‘Test
Methods for Evaluating Solid Waste,
Physical/Chemical Methods,’’ EPA
Publication SW–846, or analyzed for its
individual organic constituents.
*
*
*
*
*
(f) When an owner or operator and the
Regional Administrator do not agree on
whether a distillation, fractionation,
thin-film evaporation, solvent
extraction, or air or steam stripping
operation manages a hazardous waste
with organic concentrations of at least
10 ppmw based on knowledge of the
waste, the dispute may be resolved by
using direct measurement as specified at
paragraph (d)(1) of this section.
Subpart BB—Air Emission Standards
for Equipment Leaks
26. Section 264.1063 is amended by
revising paragraph (d)(2) to read as
follows:
I
§ 264.1063
Test methods and procedures.
*
*
*
*
*
(d) * * *
(2) Method 9060A (incorporated by
reference under 40 CFR 260.11) of ‘‘Test
Methods for Evaluating Solid Waste,’’
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*
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EPA Publication SW–846, for
computing total organic concentration
of the sample, or analyzed for its
individual organic constituents; or
*
*
*
*
*
Subpart EE—Hazardous Waste
Munitions and Explosives Storage
Appendix IX to Part 264—GroundWater Monitoring List
27. Appendix IX to part 264 is revised
as follows:
I
GROUND-WATER MONITORING LIST
Common name 1
CAS RN 2
Chemical abstracts service index name 3
Acenaphthene ............................................................................
Acenaphthylene .........................................................................
Acetone ......................................................................................
Acetophenone ............................................................................
Acetonitrile; Methyl cyanide .......................................................
2-Acetylaminofluorene; 2-AAF ...................................................
Acrolein ......................................................................................
Acrylonitrile ................................................................................
Aldrin ..........................................................................................
83–32–9 ...........
208–96–8 .........
67–64–1 ...........
98–86–2 ...........
75–05–8 ...........
53–96–3 ...........
107–02–8 .........
107–13–1 .........
309–00–2 .........
Allyl chloride ...............................................................................
4-Aminobiphenyl ........................................................................
Aniline ........................................................................................
Anthracene .................................................................................
Antimony ....................................................................................
Aramite .......................................................................................
107–05–1 .........
92–67–1 ...........
62–53–3 ...........
120–12–7 .........
(Total) ...............
140–57–8 .........
Arsenic .......................................................................................
Barium ........................................................................................
Benzene .....................................................................................
Benzo[a]anthracene; Benzanthracene ......................................
Benzo[b]fluoranthene .................................................................
Benzo[k]fluoranthene .................................................................
Benzo[ghi]perylene ....................................................................
Benzo[a]pyrene ..........................................................................
Benzyl alcohol ............................................................................
Beryllium ....................................................................................
alpha-BHC .................................................................................
beta-BHC ...................................................................................
delta-BHC ..................................................................................
gamma-BHC; Lindane ...............................................................
Bis(2-chloroethoxy)methane ......................................................
Bis(2-chloroethyl)ether ...............................................................
Bis(2-chloro-1-methylethyl)
ether;
2,2′-Dichlorodiisopropyl
ether.
Bis(2-ethylhexyl) phthalate ........................................................
Bromodichloromethane ..............................................................
Bromoform; Tribromomethane ...................................................
4-Bromophenyl phenyl ether .....................................................
Butyl benzyl phthalate; Benzyl butyl phthalate ..........................
Cadmium ....................................................................................
Carbon disulfide .........................................................................
Carbon tetrachloride ..................................................................
Chlordane ..................................................................................
(Total) ...............
(Total) ...............
71–43–2 ...........
56–55–3 ...........
205–99–2 .........
207–08–9 .........
191–24–2 .........
50–32–8 ...........
100–51–6 .........
(Total) ...............
319–84–6 .........
319–85–7 .........
319–86–8 .........
58–89–9 ...........
111–91–1 .........
111–44–4 .........
108–60–1 .........
Acenaphthylene, 1,2-dihydroAcenaphthylene
2-Propanone
Ethanone, 1-phenylAcetonitrile
Acetamide, N–9H-fluoren-2-yl2-Propenal
2-Propenenitrile
1,4:5,8-Dimethanonaphthalene,
1,2,3,4,10,10-hexachloro1,4,4a,5,8,8a-hexahydro-(1a,4a,4ab,5a,8a,8ab)1-Propene, 3-chloro[1,1′-Biphenyl]-4-amine
Benzenamine
Anthracene
Antimony
Sulfurous
acid,
2-chloroethyl
2-[4-(1,1-dimethylethyl)
phenoxy]-1-methylethyl ester
Arsenic
Barium
Benzene
Benz[a]anthracene
Benz[e]acephenanthrylene
Benzo[k]fluoranthene
Benzo[ghi]perylene
Benzo[a]pyrene
Benzenemethanol
Beryllium
Cyclohexane, 1,2,3,4,5,6-hexachloro-,(1a,2a,3b,4b,5b,6b)Cyclohexane, 1,2,3,4,5,6-hexachloro-,(1a,2b,3a,4b,5a,6b)Cyclohexane, 1,2,3,4,5,6-hexachloro-,(1a,2a,3a,4b,5a,6b)Cyclohexane, 1,2,3,4,5,6-hexachloro-,(1a,2a,3b,4a,5a,6b)Ethane, 1,1′-[methylenebis(oxy)]bis [2-chloroEthane, 1,1′-oxybis[2-chloroPropane, 2,2’-oxybis[1-chloro-
p-Chloroaniline ...........................................................................
Chlorobenzene ...........................................................................
Chlorobenzilate ..........................................................................
106–47–8 .........
108–90–7 .........
510–15–6 .........
p-Chloro-m-cresol ......................................................................
Chloroethane; Ethyl chloride .....................................................
Chloroform .................................................................................
2-Chloronaphthalene .................................................................
2-Chlorophenol ..........................................................................
4-Chlorophenyl phenyl ether .....................................................
Chloroprene ...............................................................................
Chromium ..................................................................................
Chrysene ....................................................................................
Cobalt .........................................................................................
Copper .......................................................................................
m-Cresol ....................................................................................
o-Cresol .....................................................................................
p-Cresol .....................................................................................
Cyanide ......................................................................................
2,4-D; 2,4-Dichlorophenoxyacetic acids ....................................
59–50–7 ...........
75–00–3 ...........
67–66–3 ...........
91–58–7 ...........
95–57–8 ...........
7005–72–3 .......
126–99–8 .........
(Total) ...............
218–01–9 .........
(Total) ...............
(Total) ...............
108–39–4 .........
95–48–7 ...........
106–44–5 .........
57–12–5 ...........
94–75–7 ...........
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117–81–7 .........
75–27–4 ...........
75–25–2 ...........
101–55–3 .........
85–68–7 ...........
(Total) ...............
75–15–0 ...........
56–23–5 ...........
57–74–9 ...........
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1,2-Benzenedicarboxylic acid, bis(2-ethylhexyl)ester
Methane, bromodichloroMethane, tribromoBenzene, 1-bromo-4-phenoxy1,2-Benzenedicarboxylic acid, butyl phenylmethyl ester
Cadmium
Carbon disulfide
Methane, tetrachloro4,7-Methano-1H-indene,
1,2,4,5,6,7,8,8-octachloro2,3,3a,4,7,7a -hexahydroBenzenamine, 4-chloroBenzene, chloroBenzeneacetic acid, 4-chloro-a-(4-chlorophenyl)-a-hydroxy-,
ethyl ester
Phenol, 4-chloro-3-methylEthane, chloroMethane, trichloroNaphthalene, 2-chloroPhenol, 2-chloroBenzene, 1-chloro-4-phenoxy1,3-Butadiene,2-chloroChromium
Chrysene
Cobalt
Copper
Phenol, 3-methylPhenol, 2-methylPhenol, 4-methylCyanide
Acetic acid, (2,4-dichlorophenoxy)-
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GROUND-WATER MONITORING LIST—Continued
Common name 1
CAS RN 2
Chemical abstracts service index name 3
4,4′-DDD ....................................................................................
4,4′-DDE ....................................................................................
4,4′-DDT .....................................................................................
Diallate .......................................................................................
72–54–8 ...........
72–55–9 ...........
50–29–3 ...........
2303–16–4 .......
Dibenz[a,h]anthracene ...............................................................
Dibenzofuran ..............................................................................
Dibromochloromethane; Chlorodibromomethane ......................
1,2-Dibromo-3-chloropropane; DBCP ........................................
1,2-Dibromoethane; Ethylene dibromide ...................................
Di-n-butyl phthalate ....................................................................
o-Dichlorobenzene .....................................................................
m-Dichlorobenzene ....................................................................
p-Dichlorobenzene .....................................................................
3,3′-Dichlorobenzidine ...............................................................
trans-1,4-Dichloro-2-butene .......................................................
Dichlorodifluoromethane ............................................................
1,1-Dichloroethane .....................................................................
1,2-Dichloroethane; Ethylene dichloride ....................................
1,1-Dichloroethylene; Vinylidene chloride .................................
trans-1,2-Dichloroethylene .........................................................
2,4-Dichlorophenol .....................................................................
2,6-Dichlorophenol .....................................................................
1,2-Dichloropropane ..................................................................
cis-1,3-Dichloropropene .............................................................
trans-1,3-Dichloropropene .........................................................
Dieldrin .......................................................................................
53–70–3 ...........
132–64–9 .........
124–48–1 .........
96–12–8 ...........
106–93–4 .........
84–74–2 ...........
95–50–1 ...........
541–73–1 .........
106–46–7 .........
91–94–1 ...........
110–57–6 .........
75–71–8 ...........
75–34–3 ...........
107–06–2 .........
75–35–4 ...........
156–60–5 .........
120–83–2 .........
87–65–0 ...........
78–87–5 ...........
10061–01–5 .....
10061–02–6 .....
60–57–1 ...........
Diethyl phthalate ........................................................................
O,O-Diethyl O-2-pyrazinyl phosphorothioate; Thionazin ...........
Dimethoate .................................................................................
84–66–2 ...........
297–97–2 .........
60–51–5 ...........
p-(Dimethylamino)azobenzene ..................................................
7,12-Dimethylbenz[a]anthracene ...............................................
3,3′-Dimethylbenzidine ...............................................................
alpha, alpha-Dimethylphenethylamine .......................................
2,4-Dimethylphenol ....................................................................
Dimethyl phthalate .....................................................................
m-Dinitrobenzene .......................................................................
4,6-Dinitro-o-cresol ....................................................................
2,4-Dinitrophenol ........................................................................
2,4-Dinitrotoluene .......................................................................
2,6-Dinitrotoluene .......................................................................
Dinoseb; DNBP; 2-sec-Butyl-4,6-dinitrophenol .........................
Di-n-octyl phthalate ....................................................................
1,4-Dioxane ................................................................................
Diphenylamine ...........................................................................
Disulfoton ...................................................................................
Endosulfan I ...............................................................................
60–11–7 ...........
57–97–6 ...........
119–93–7 .........
122–09–8 .........
105–67–9 .........
131–11–3 .........
99–65–0 ...........
534–52–1 .........
51–28–5 ...........
121–14–2 .........
606–20–2 .........
88–85–7 ...........
117–84–0 .........
123–91–1 .........
122–39–4 .........
298–04–4 .........
959–98–8 .........
Endosulfan II ..............................................................................
33213–65–9 .....
Endosulfan sulfate .....................................................................
1031–07–8 .......
Endrin .........................................................................................
72–20–8 ...........
Endrin aldehyde .........................................................................
7421–93–4 .......
Ethylbenzene .............................................................................
Ethyl methacrylate .....................................................................
Ethyl methanesulfonate .............................................................
Famphur .....................................................................................
100–41–4 .........
97–63–2 ...........
62–50–0 ...........
52–85–7 ...........
Fluoranthene ..............................................................................
Fluorene .....................................................................................
Heptachlor ..................................................................................
206–44–0 .........
86–73–7 ...........
76–44–8 ...........
Benzene 1,1′-(2,2-dichloroethylidene) bis[4-chloroBenzene, 1,1′-(dichloroethenylidene) bis[4-chloroBenzene, 1,1′-(2,2,2-trichloroethylidene) bis[4-chloroCarbamothioic acid, bis(1-methylethyl)- , S- (2,3-dichloro-2propenyl) ester
Dibenz[a,h]anthracene
Dibenzofuran
Methane, dibromochloroPropane, 1,2-dibromo-3-chloroEthane, 1,2-dibromo1,2-Benzenedicarboxylic acid, dibutyl ester
Benzene, 1,2-dichloroBenzene, 1,3-dichloroBenzene, 1,4-dichloro[1,1′-Biphenyl]-4,4′-diamine, 3,3′-dichloro2-Butene, 1,4-dichloro-, (E)Methane, dichlorodifluoroEthane, 1,1-dichloroEthane, 1,2-dichloroEthene, 1,1-dichloroEthene, 1,2-dichloro-, (E)Phenol, 2,4-dichloroPhenol, 2,6-dichloroPropane, 1,2-dichloro1-Propene, 1,3-dichloro-, (Z)1-Propene, 1,3-dichloro-, (E)2,7:3,6-Dimethanonaphth
[2,3-b]oxirene,
3,4,5,6,9,9hexachloro-1a,2,2a,3,6,6a,7,7a-octahydro-,
(1aa,2b,2aa,3b,6b;,6aa,7b,7aa)1,2-Benzenedicarboxylic acid, diethyl ester
Phosphorothioic acid, O,O-diethyl O-pyrazinyl ester
Phosphorodithioic acid, O,O-dimethyl S-[2-(methylamino)-2oxoethyl] ester
Benzenamine, N,N-dimethyl-4-(phenylazo)Benz[a]anthracene, 7,12-dimethyl[1,1′-Biphenyl]-4,4′-diamine, 3,3′-dimethylBenzeneethanamine, a,a-dimethylPhenol, 2,4-dimethyl1,2-Benzenedicarboxylic acid, dimethyl ester
Benzene, 1,3-dinitroPhenol, 2-methyl-4,6-dinitroPhenol, 2,4-dinitroBenzene, 1-methyl-2,4-dinitroBenzene, 2-methyl-1,3-dinitroPhenol, 2-(1-methylpropyl)-4,6-dinitro1,2-Benzenedicarboxylic acid, dioctyl ester
1,4-Dioxane
Benzenamine, N-phenylPhosphorodithioic acid, O,O-diethyl S-[2-(ethylthio)ethyl]ester
6,9-Methano-2,4,3benzodioxathiepin,
6,7,8,9,10,10hexachloro-1,5,5a,6,9,9a-hexahydro-,
3oxide,(3a,5ab,6a,9a,9ab)6,9-Methano-2,4,3benzodioxathiepin,
6,7,8,9,10,10hexachloro-1,5,5a,6,9,9a-hexahydro-,
3-oxide,
(3a,5aa,6b,9b,9aa)6,9-Methano-2,4,3benzodioxathiepin,
6,7,8,9,10,10hexachloro-1,5,5a,6,9,9a-hexahydro-, 3,3-dioxide
2,7:3,6-Dimethanonaphth[2,3-b]oxirene,
3,4,5,6,9,9hexachloro-,1a,2,2a,3,6,6a,7,7a-octahydro-,
(1aa,2b,2ab,3a,6a,6ab,7b, 7aa)1,2,4- Methenocyclopenta[cd] pentalene-5-carboxaldehyde,
2,2a,3,3,4,7-hexachlorodecahydro-,(1a,2b,2ab,4b,4ab,
5b,6ab,6bb,7R*)Benzene, ethyl2-Propenoic acid, 2-methyl-, ethyl ester
Methanesulfonic acid, ethyl ester
Phosphorothioic acid, O-[4-[(dimethylamino)sulfonyl]phenyl]O,O-dimethyl ester
Fluoranthene
9H-Fluorene
4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7atetrahydro-
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GROUND-WATER MONITORING LIST—Continued
Common name 1
CAS RN 2
Chemical abstracts service index name 3
Heptachlor epoxide ....................................................................
1024–57–3 .......
Hexachlorobenzene ...................................................................
Hexachlorobutadiene .................................................................
Hexachlorocyclopentadiene .......................................................
Hexachloroethane ......................................................................
Hexachlorophene .......................................................................
Hexachloropropene ....................................................................
2-Hexanone ...............................................................................
Indeno(1,2,3-cd)pyrene ..............................................................
Isobutyl alcohol ..........................................................................
Isodrin ........................................................................................
118–74–1 .........
87–68–3 ...........
77–47–4 ...........
67–72–1 ...........
70–30–4 ...........
1888–71–7 .......
591–78–6 .........
193–39–5 .........
78–83–1 ...........
465–73–6 .........
Isophorone .................................................................................
Isosafrole ...................................................................................
Kepone .......................................................................................
78–59–1 ...........
120–58–1 .........
143–50–0 .........
Lead ...........................................................................................
Mercury ......................................................................................
Methacrylonitrile .........................................................................
Methapyrilene ............................................................................
(Total) ...............
(Total) ...............
126–98–7 .........
91–80–5 ...........
Methoxychlor ..............................................................................
Methyl bromide; Bromomethane ...............................................
Methyl chloride; Chloromethane ................................................
3-Methylcholanthrene ................................................................
Methylene bromide; Dibromomethane ......................................
Methylene chloride; Dichloromethane .......................................
Methyl ethyl ketone; MEK; .........................................................
Methyl iodide; Iodomethane ......................................................
Methyl methacrylate ...................................................................
Methyl methanesulfonate ...........................................................
2-Methylnaphthalene .................................................................
Methyl parathion; Parathion methyl ...........................................
4-Methyl-2-pentanone; Methyl isobutyl ketone ..........................
Naphthalene ...............................................................................
1,4-Naphthoquinone ..................................................................
1-Naphthylamine ........................................................................
2-Naphthylamine ........................................................................
Nickel .........................................................................................
o-Nitroaniline ..............................................................................
m-Nitroaniline .............................................................................
p-Nitroaniline ..............................................................................
Nitrobenzene ..............................................................................
o-Nitrophenol .............................................................................
p-Nitrophenol .............................................................................
4-Nitroquinoline 1-oxide .............................................................
N-Nitrosodi-n-butylamine ...........................................................
N-Nitrosodiethylamine ................................................................
N-Nitrosodimethylamine .............................................................
N-Nitrosodiphenylamine .............................................................
N-Nitrosodipropylamine;Di-n-propylnitrosamine ........................
N-Nitrosomethylethalamine ........................................................
N-Nitrosomorpholine ..................................................................
N-Nitrosopiperidine ....................................................................
N-Nitrosopyrrolidine ...................................................................
5-Nitro-o-toluidine ......................................................................
Parathion ....................................................................................
Polychlorinated biphenyls; PCBs ...............................................
Polychlorinated dibenzo-p-dioxins; PCDDs ...............................
Polychlorinated dibenzofurans; PCDFs .....................................
Pentachlorobenzene ..................................................................
Pentachloroethane .....................................................................
Pentachloronitrobenzene ...........................................................
Pentachlorophenol .....................................................................
Phenacetin .................................................................................
Phenanthrene ............................................................................
Phenol ........................................................................................
p-Phenylenediamine ..................................................................
Phorate ......................................................................................
72–43–5 ...........
74–83–9 ...........
74–87–3 ...........
56–49–5 ...........
74–95–3 ...........
75–09–2 ...........
78–93–3 ...........
74–88–4 ...........
80–62–6 ...........
66–27–3 ...........
91–57–6 ...........
298–00–0 .........
108–10–1 .........
91–20–3 ...........
130–15–4 .........
134–32–7 .........
91–59–8 ...........
(Total) ...............
88–74–4 ...........
99–09–2 ...........
100–01–6 .........
98–95–3 ...........
88–75–5 ...........
100–02–7 .........
56–57–5 ...........
924–16–3 .........
55–18–5 ...........
62–75–9 ...........
86–30–6 ...........
621–64–7 .........
10595–95–6 .....
59–89–2 ...........
100–75–4 .........
930–55–2 .........
99–55–8 ...........
56–38–2 ...........
See footnote 4 ..
See footnote 5 ..
See footnote 6 ..
608–93–5 .........
76–01–7 ...........
82–68–8 ...........
87–86–5 ...........
62–44–2 ...........
85–01–8 ...........
108–95–2 .........
106–50–3 .........
298–02–2 .........
2,5-Methano-2H-indeno[1,2-b]
oxirene,
2,3,4,5,6,7,7heptachloro-1a,1b,5,5a,6,6a,-hexahydro-,
(1aa,1bb,2a,5a,5ab,6b,6aa)
Benzene, hexachloro1,3-Butadiene, 1,1,2,3,4,4-hexachloro1,3-Cyclopentadiene, 1,2,3,4,5,5-hexachloroEthane, hexachloroPhenol, 2,2′-methylenebis[3,4,6-trichloro1-Propene, 1,1,2,3,3,3-hexachloro2-Hexanone
Indeno[1,2,3-cd]pyrene
1-Propanol, 2-methyl1,4,5,8-Dimethanonaphthalene,1,2,3,4,1
0,10-hexachloro1,4,4a,5,8,8a hexahydro-(1a, 4a, 4ab, 5b, 8b, 8ab)2-Cyclohexen-1-one, 3,5,5-trimethyl1,3-Benzodioxole, 5-(1-propenyl)1,3,4-Metheno-2H-cyclobuta-[cd]pentalen-2-one,
1,1a,3,3a,4,5,5,5a,5b,6-decachlorooctahydroLead
Mercury
2-Propenenitrile, 2-methyl1,2,Ethanediamine,N,N-dimethyl-N′-2-pyridinyl-N′-(2thienylmethyl)Benzene, 1,1′-(2,2,2,trichloroethylidene)bis [4-methoxyMethane, bromoMethane, chloroBenz[j]aceanthrylene, 1,2-dihydro-3-methylMethane, dibromoMethane, dichloro2-Butanone
Methane, iodo2-Propenoic acid, 2-methyl-, methyl ester
Methanesulfonic acid, methyl ester
Naphthalene, 2-methylPhosphorothioic acid, O,O-dimethyl O=(4-nitrophenyl) ester
2-Pentanone, 4-methylNaphthalene
1,4-Naphthalenedione
1-Naphthalenamine
2-Naphthalenamine
Nickel
Benzenamine, 2-nitroBenzenamine, 3-nitroBenzenamine, 4-nitroBenzene, nitroPhenol, 2-nitroPhenol, 4-nitroQuinoline, 4-nitro, 1-oxide
1-Butanamine, N-butyl-N-nitrosoEthanamine, N-ethyl-N-nitrosoMethanamine, N-methyl-N-nitrosoBenzenamine, N-nitroso-N-phenyl1-Propanamine, N-nitroso-N-propylEthanamine, N-methyl-N-nitrosoMorpholine, 4-nitrosoPiperidine, 1-nitrosoPyrrolidine, 1-nitrosoBenzenamine, 2-methyl-5-nitroPhosphorothioic acid, O,O-diethyl-O-(4-nitrophenyl) ester
1,1′-Biphenyl, chloro derivatives
Dibenzo[b,e][1,4]dioxin, chloro derivatives
Dibenzofuran, chloro derivatives
Benzene, pentachloroEthane, pentachloroBenzene, pentachloronitroPhenol, pentachloroAcetamide, N-(4-ethoxyphenyl)
Phenanthrene
Phenol
1,4-Benzenediamine
Phosphorodithioic acid, O,O-diethyl S- [(ethylthio)methyl]
ester
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GROUND-WATER MONITORING LIST—Continued
Common name 1
CAS RN 2
2-Picoline ...................................................................................
Pronamide ..................................................................................
Propionitrile; Ethyl cyanide ........................................................
Pyrene ........................................................................................
Pyridine ......................................................................................
Safrole ........................................................................................
Selenium ....................................................................................
Silver ..........................................................................................
Silvex; 2,4,5-TP .........................................................................
Styrene .......................................................................................
Sulfide ........................................................................................
2,4,5-T; 2,4,5-Trichlorophenoxyacetic acid ...............................
2,3,7,8-TCDD; 2,3,7,8-Tetrachlorodibenzo-p-dioxin ..................
1,2,4,5-Tetrachlorobenzene .......................................................
1,1,1,2-Tetrachloroethane ..........................................................
1,1,2,2-Tetrachloroethane ..........................................................
Tetrachloroethylene; Perchloroethylene; Tetrachloroethene .....
2,3,4,6-Tetrachlorophenol ..........................................................
Tetraethyl dithiopyrophosphate; Sulfotepp ................................
Thallium .....................................................................................
Tin ..............................................................................................
Toluene ......................................................................................
o-Toluidine .................................................................................
Toxaphene .................................................................................
1,2,4-Trichlorobenzene ..............................................................
1,1,1-Trichloroethane; Methylchloroform ...................................
1,1,2-Trichloroethane .................................................................
Trichloroethylene; Trichloroethene ............................................
Trichlorofluoromethane ..............................................................
2,4,5-Trichlorophenol .................................................................
2,4,6-Trichlorophenol .................................................................
1,2,3-Trichloropropane ...............................................................
O,O,O-Triethyl phosphorothioate ...............................................
sym-Trinitrobenzene ..................................................................
Vanadium ...................................................................................
Vinyl acetate ..............................................................................
Vinyl chloride .............................................................................
Xylene (total) ..............................................................................
Zinc ............................................................................................
109–06–8 .........
23950–58–5 .....
107–12–0 .........
129–00–0 .........
110–86–1 .........
94–59–7 ...........
(Total) ...............
(Total) ...............
93–72–1 ...........
100–42–5 .........
18496–25–8 .....
93–76–5 ...........
1746–01–6 .......
95–94–3 ...........
630–20–6 .........
79–34–5 ...........
127–18–4 .........
58–90–2 ...........
3689–24–5 .......
(Total) ...............
(Total) ...............
108–88–3 .........
95–53–4 ...........
8001–35–2 .......
120–82–1 .........
71–55–6 ...........
79–00–5 ...........
79–01–6 ...........
75–69–4 ...........
95–95–4 ...........
88–06–2 ...........
96–18–4 ...........
126–68–1 .........
99–35–4 ...........
(Total) ...............
108–05–4 .........
75–01–4 ...........
1330–20–7 .......
(Total) ...............
Chemical abstracts service index name 3
Pyridine, 2-methylBenzamide, 3,5-dichloro-N-(1,1-dimethyl-2-propynyl)Propanenitrile
Pyrene
Pyridine
1,3-Benzodioxole, 5-(2-propenyl)Selenium
Silver
Propanoic acid, 2-(2,4,5- trichlorophenoxy)Benzene, ethenylSulfide
Acetic acid, (2,4,5-trichlorophenoxy)Dibenzo[b,e][1,4]dioxin, 2,3,7,8-tetrachloroBenzene, 1,2,4,5-tetrachloroEthane, 1,1,1,2-tetrachloroEthane, 1,1,2,2-tetrachloroEthene, tetrachloroPhenol, 2,3,4,6-tetrachloroThiodiphosphoric acid ([(HO)2 P(S)]2 O), tetraethyl ester
Thallium
Tin
Benzene, methylBenzenamine, 2-methylToxaphene
Benzene, 1,2,4-trichloroEthane, 1,1,1-trichloroEthane, 1,1,2-trichloroEthene, trichloroMethane, trichlorofluoroPhenol, 2,4,5-trichloroPhenol, 2,4,6-trichloroPropane, 1,2,3-trichloroPhosphorothioic acid, O,O,O-triethyl ester
Benzene, 1,3,5-trinitroVanadium
Acetic acid, ethenyl ester
Ethene, chloroBenzene, dimethylZinc
1 Common names are those widely used in government regulations, scientific publications, and commerce; synonyms exist for many chemicals.
2 Chemical Abstracts Service registry number. Where ‘‘Total’’ is entered, all species in the ground water that contain this element are included.
3 CAS index names are those used in the 9th Cumulative Index.
4 Polychlorinated biphenyls (CAS RN 1336–36–3); this category contains congener chemicals, including constituents of Aroclor-1016 (CAS RN
12674–11–2), Aroclor-1221 (CAS RN 11104–28–2), Aroclor-1232 (CAS RN 11141–16–5), Aroclor-1242 (CAS RN 53469–21–9), Aroclor-1248
(CAS RN 12672–29–6), Aroclor-1254 (CAS RN 11097–69–1), and Aroclor-1260 (CAS RN 11096–82–5).
5 This category contains congener chemicals, including tetrachlorodibenzo-p-dioxins (see also 2,3,7,8-TCDD), pentachlorodibenzo-p-dioxins,
and hexachlorodibenzo-p-dioxins.
6 This category contains congener chemicals, including tetrachlorodibenzofurans, pentachlorodibenzofurans, and hexachlorodibenzofurans.
PART 265—INTERIM STATUS
STANDARDS FOR OWNERS AND
OPERATORS OF HAZARDOUS WASTE
TREATMENT, STORAGE, AND
DISPOSAL FACILITIES
28. The authority citation for part 265
continues to read as follows:
I
Authority: 42 U.S.C. 6905, 6906, 6912,
6922, 6923, 6924, 6925, 6935, 6936 and 6937,
unless otherwise noted.
Subpart J—Tank Systems
29. Section 265.190 is amended by
revising paragraph (a) to read as follows:
I
§ 265.190
Applicability.
*
*
(a) Tank systems that are used to store
or treat hazardous waste which contains
no free liquids and are situated inside
a building with an impermeable floor
are exempted from the requirements in
§ 265.193. To demonstrate the absence
or presence of free liquids in the stored/
treated waste, the following test must be
used: Method 9095B (Paint Filter
Liquids Test) as described in ‘‘Test
Methods for Evaluating Solid Waste,
Physical/Chemical Methods,’’ EPA
Publication SW–846, as incorporated by
reference in § 260.11 of this chapter.
*
*
*
*
*
*
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*
*
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Subpart N—Landfills
30. Section 265.314 is amended by
revising paragraph (d) to read as follows:
I
§ 265.314 Special requirements for bulk
and containerized liquids.
*
*
*
*
*
(d) To demonstrate the absence or
presence of free liquids in either a
containerized or a bulk waste, the
following test must be used: Method
9095B (Paint Filter Liquids Test) as
described in ‘‘Test Methods for
Evaluating Solid Waste, Physical/
Chemical Methods,’’ EPA Publication
SW–846, as incorporated by reference in
§ 260.11 of this chapter.
*
*
*
*
*
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Federal Register / Vol. 70, No. 113 / Tuesday, June 14, 2005 / Rules and Regulations
Subpart AA—Air Emission Standards
for Process Vents
31. Section 265.1034 is amended by
revising paragraphs (c)(1)(ii), (c)(1)(iv),
(d)(1)(iii) and (f) to read as follows:
I
§ 265.1034
Test methods and procedures.
*
*
*
*
*
(c) * * *
(1) * * *
(ii) Method 18 or Method 25A in 40
CFR part 60, appendix A, for organic
content. If Method 25A is used, the
organic HAP used as the calibration gas
must be the single organic HAP
representing the largest percent by
volume of the emissions. The use of
Method 25A is acceptable if the
response from the high-level calibration
gas is at least 20 times the standard
deviation of the response from the zero
calibration gas when the instrument is
zeroed on the most sensitive scale.
*
*
*
*
*
(iv) Total organic mass flow rates
shall be determined by the following
equation:
(A) For sources utilizing Method 18.
n
E h = Q 2sd ∑ C i MWi [0.0416] 10 −6
i =1
[
]
Where:
Eh = Total organic mass flow rate, kg/h;
Q2sd = Volumetric flow rate of gases
entering or exiting control device,
as determined by Method 2, dscm/
h;
n = Number of organic compounds in
the vent gas;
Ci = Organic concentration in ppm, dry
basis, of compound i in the vent
gas, as determined by Method 18;
MWi = Molecular weight of organic
compound i in the vent gas, kg/kgmol;
0.0416 = Conversion factor for molar
volume, kg-mol/m3 (@ 293 K and
760 mm Hg);
10¥6 = Conversion from ppm
(B) For sources utilizing Method 25A.
Eh = (Q)(C)(MW)(0.0416)(10¥6)
Where:
Eh = Total organic mass flow rate, kg/h;
Q = Volumetric flow rate of gases
entering or exiting control device,
as determined by Method 2, dscm/
h;
C = Organic concentration in ppm, dry
basis, as determined by Method
25A;
MW = Molecular weight of propane, 44;
0.0416 = Conversion factor for molar
volume, kg-mol/m3 (@ 293 K and
760 mm Hg);
10¥6 = Conversion from ppm.
*
*
*
*
*
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(d) * * *
(1) * * *
(iii) Each sample shall be analyzed
and the total organic concentration of
the sample shall be computed using
Method 9060A (incorporated by
reference under § 260.11 of this chapter)
of ‘‘Test Methods for Evaluating Solid
Waste, Physical/Chemical Methods,’’
EPA Publication SW–846; or analyzed
for its individual organic constituents.
*
*
*
*
*
(f) When an owner or operator and the
Regional Administrator do not agree on
whether a distillation, fractionation,
thin-film evaporation, solvent
extraction, or air or steam stripping
operation manages a hazardous waste
with organic concentrations of at least
10 ppmw based on knowledge of the
waste, the dispute may be resolved
using direct measurement as specified at
paragraph (d)(1) of this section.
Subpart BB—Air Emission Standards
for Equipment Leaks
32. Section 265.1063 is amended by
revising paragraph (d)(2) to read as
follows:
I
§ 265.1063
Test methods and procedures.
*
*
*
*
*
(d) * * *
(2) Method 9060A (incorporated by
reference under § 260.11 of this chapter)
of ‘‘Test Methods for Evaluating Solid
Waste,’’ EPA Publication SW–846 or
analyzed for its individual organic
constituents; or
*
*
*
*
*
Subpart CC—Air Emission Standards
for Tanks, Surface Impoundments, and
Containers
33. Section 265.1081 is amended by
revising the definition ‘‘Waste
stabilization process’’ to read as follows:
I
§ 265.1081
Definitions.
*
*
*
*
*
Waste stabilization process means any
physical or chemical process used to
either reduce the mobility of hazardous
constituents in a hazardous waste or
eliminate free liquids as determined by
Test Method 9095B (Paint Filter Liquids
Test) in ‘‘Test Methods for Evaluating
Solid Waste, Physical/Chemical
Methods,’’ EPA Publication SW–846, as
incorporated by reference in § 260.11. A
waste stabilization process includes
mixing the hazardous waste with
binders or other materials, and curing
the resulting hazardous waste and
binder mixture. Other synonymous
terms used to refer to this process are
‘‘waste fixation’’ or ‘‘waste
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solidification.’’ This does not include
the adding of absorbent materials to the
surface of a waste, without mixing,
agitation, or subsequent curing, to
absorb free liquid.
I 34. Section 265.1084 is amended by
revising paragraphs (a)(3)(ii)(C),
(a)(3)(iii), (b)(3)(ii)(C), (b)(3)(iii), and
(c)(3)(i) to read as follows:
§ 265.1084 Waste determination
procedures.
(a) * * *
(3) * * *
(ii) * * *
(C) All samples shall be collected and
handled in accordance with written
procedures prepared by the owner or
operator and documented in a site
sampling plan. This plan shall describe
the procedure by which representative
samples of the hazardous waste stream
are collected such that a minimum loss
of organics occurs throughout the
sample collection and handling process,
and by which sample integrity is
maintained. A copy of the written
sampling plan shall be maintained onsite in the facility operating records. An
example of acceptable sample collection
and handling procedures for a total
volatile organic constituent
concentration may be found in Method
25D in 40 CFR part 60, appendix A.
*
*
*
*
*
(iii) Analysis. Each collected sample
shall be prepared and analyzed in
accordance with Method 25D in 40 CFR
part 60, appendix A for the total
concentration of volatile organic
constituents, or using one or more
methods when the individual organic
compound concentrations are identified
and summed and the summed waste
concentration accounts for and reflects
all organic compounds in the waste
with Henry’s law constant values at
least 0.1 mole-fraction-in-the-gas-phase/
mole-fraction-in-the-liquid-phase (0.1
Y/X) [which can also be expressed as
1.8 × 10¥6 atmospheres/gram-mole/m3]
at 25 degrees Celsius. At the owner or
operator’s discretion, the owner or
operator may adjust test data obtained
by any appropriate method to discount
any contribution to the total volatile
organic concentration that is a result of
including a compound with a Henry’s
law constant value of less than 0.1 Y/X
at 25 degrees Celsius. To adjust these
data, the measured concentration of
each individual chemical constituent
contained in the waste is multiplied by
the appropriate constituent-specific
adjustment factor (fm25D). If the owner or
operator elects to adjust test data, the
adjustment must be made to all
individual chemical constituents with a
Henry’s law constant value greater than
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or equal to 0.1 Y/X at 25 degrees Celsius
contained in the waste. Constituentspecific adjustment factors (fm25D) can
be obtained by contacting the Waste and
Chemical Processes Group, Office of Air
Quality Planning and Standards,
Research Triangle Park, NC 27711.
Other test methods may be used if they
meet the requirements in paragraph
(a)(3)(iii)(A) or (B) of this section and
provided the requirement to reflect all
organic compounds in the waste with
Henry’s law constant values greater than
or equal to 0.1 Y/X [which can also be
expressed as 1.8 x 10¥6 atmospheres/
gram-mole/m3] at 25 degrees Celsius, is
met.
(A) Any EPA standard method that
has been validated in accordance with
‘‘Alternative Validation Procedure for
EPA Waste and Wastewater Methods,’’
40 CFR part 63, appendix D.
(B) Any other analysis method that
has been validated in accordance with
the procedures specified in Section 5.1
or Section 5.3, and the corresponding
calculations in Section 6.1 or Section
6.3, of Method 301 in 40 CFR part 63,
appendix A. The data are acceptable if
they meet the criteria specified in
Section 6.1.5 or Section 6.3.3 of Method
301. If correction is required under
section 6.3.3 of Method 301, the data are
acceptable if the correction factor is
within the range 0.7 to 1.30. Other
sections of Method 301 are not required.
*
*
*
*
*
(b) * * *
(3) * * *
(ii) * * *
(C) All samples shall be collected and
handled in accordance with written
procedures prepared by the owner or
operator and documented in a site
sampling plan. This plan shall describe
the procedure by which representative
samples of the hazardous waste stream
are collected such that a minimum loss
of organics occurs throughout the
sample collection and handling process,
and by which sample integrity is
maintained. A copy of the written
sampling plan shall be maintained onsite in the facility operating records. An
example of acceptable sample collection
and handling procedures for a total
volatile organic constituent
concentration may be found in Method
25D in 40 CFR part 60, appendix A.
*
*
*
*
*
(iii) Analysis. Each collected sample
shall be prepared and analyzed in
accordance with Method 25D in 40 CFR
part 60, appendix A for the total
concentration of volatile organic
constituents, or using one or more
methods when the individual organic
compound concentrations are identified
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and summed and the summed waste
concentration accounts for and reflects
all organic compounds in the waste
with Henry’s law constant values at
least 0.1 mole-fraction-in-the-gas-phase/
mole-fraction-in-the-liquid-phase (0.1
Y/X) [which can also be expressed as
1.8 x 10¥6 atmospheres/gram-mole/m3]
at 25 degrees Celsius. When the owner
or operator is making a waste
determination for a treated hazardous
waste that is to be compared to an
average VO concentration at the point of
waste origination or the point of waste
entry to the treatment system to
determine if the conditions of
§ 264.1082(c)(2)(i) through (c)(2)(vi) of
this chapter, or § 265.1083(c)(2)(i)
through (c)(2)(vi) of this subpart are met,
then the waste samples shall be
prepared and analyzed using the same
method or methods as were used in
making the initial waste determinations
at the point of waste origination or at
the point of entry to the treatment
system. At the owner or operator’s
discretion, the owner or operator may
adjust test data obtained by any
appropriate method to discount any
contribution to the total volatile organic
concentration that is a result of
including a compound with a Henry’s
law constant value less than 0.1 Y/X at
25 degrees Celsius. To adjust these data,
the measured concentration of each
individual chemical constituent in the
waste is multiplied by the appropriate
constituent-specific adjustment factor
(fm25D). If the owner or operator elects to
adjust test data, the adjustment must be
made to all individual chemical
constituents with a Henry’s law
constant value greater than or equal to
0.1 Y/X at 25 degrees Celsius contained
in the waste. Constituent-specific
adjustment factors (fm25D) can be
obtained by contacting the Waste and
Chemical Processes Group, Office of Air
Quality Planning and Standards,
Research Triangle Park, NC 27711.
Other test methods may be used if they
meet the requirements in paragraph
(a)(3)(iii)(A) or (B) of this section and
provided the requirement to reflect all
organic compounds in the waste with
Henry’s law constant values greater than
or equal to 0.1 Y/X [which can also be
expressed as 1.8 x 10¥6 atmospheres/
gram-mole/m3] at 25 degrees Celsius, is
met.
(A) Any EPA standard method that
has been validated in accordance with
‘‘Alternative Validation Procedure for
EPA Waste and Wastewater Methods,’’
40 CFR part 63, appendix D.
(B) Any other analysis method that
has been validated in accordance with
the procedures specified in Section 5.1
or Section 5.3, and the corresponding
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calculations in Section 6.1 or Section
6.3, of Method 301 in 40 CFR part 63,
appendix A. The data are acceptable if
they meet the criteria specified in
Section 6.1.5 or Section 6.3.3 of Method
301. If correction is required under
section 6.3.3 of Method 301, the data are
acceptable if the correction factor is
within the range 0.7 to 1.30. Other
sections of Method 301 are not required.
*
*
*
*
*
(c) * * *
(3) * * *
(i) Sampling. A sufficient number of
samples shall be collected to be
representative of the waste contained in
the tank. All samples shall be collected
and handled in accordance with written
procedures prepared by the owner or
operator and documented in a site
sampling plan. This plan shall describe
the procedure by which representative
samples of the hazardous waste are
collected such that a minimum loss of
organics occurs throughout the sample
collection and handling process and by
which sample integrity is maintained. A
copy of the written sampling plan shall
be maintained on-site in the facility
operating records. An example of
acceptable sample collection and
handling procedures may be found in
Method 25D in 40 CFR part 60,
appendix A.
*
*
*
*
*
PART 266—STANDARDS FOR THE
MANAGEMENT OF SPECIFIC
HAZARDOUS WASTES AND SPECIFIC
TYPES OF HAZARDOUS WASTE
MANAGEMENT FACILITIES
35. The authority citation for part 266
continues to read as follows:
I
Authority: 42 U.S.C. 1006, 2002(a), 3001–
3009, 3014, 6905, 6906, 6912, 6922, 6924–
6927, 6934 and 6937.
Subpart H—Hazardous Waste Burned
in Boilers and Industrial Furnaces
36. Section 266.100 is amended by
revising paragraphs (d)(1)(ii) and (g)(2) to
read as follows:
I
§ 266.100
Applicability.
*
*
*
*
*
(d) * * *
(1) * * *
(ii) Sample and analyze the hazardous
waste and other feedstocks as necessary
to comply with the requirements of this
paragraph by using appropriate
methods; and
*
*
*
*
*
(g) * * *
(2) Sample and analyze the hazardous
waste as necessary to document that the
waste contains economically significant
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amounts of the metals and that the
treatment recovers economically
significant amounts of precious metal;
and
*
*
*
*
*
I 37. Section 266.102 is amended by
revising paragraph (b)(1) to read as
follows:
§ 266.102
Permit standards for burners.
*
*
*
*
*
(b) * * * (1) The owner or operator
must provide an analysis of the
hazardous waste that quantifies the
concentration of any constituent
identified in appendix VIII of part 261
of this chapter that may reasonably be
expected to be in the waste. Such
constituents must be identified and
quantified if present, at levels detectable
by using appropriate analytical
procedures. The appendix VIII, part 261
constituents excluded from this analysis
must be identified and the basis for their
exclusion explained. This analysis will
be used to provide all information
required by this subpart and §§ 270.22
and 270.66 of this chapter and to enable
the permit writer to prescribe such
permit conditions as necessary to
protect human health and the
environment. Such analysis must be
included as a portion of the part B
permit application, or, for facilities
operating under the interim status
standards of this subpart, as a portion of
the trial burn plan that may be
submitted before the part B application
under provisions of § 270.66(g) of this
chapter as well as any other analysis
required by the permit authority in
preparing the permit. Owners and
operators of boilers and industrial
furnaces not operating under the interim
status standards must provide the
information required by §§ 270.22 or
270.66(c) of this chapter in the part B
application to the greatest extent
possible.
*
*
*
*
*
I 38. Section 266.106 is amended by
revising paragraph (a) to read as follows:
§ 266.106 Standards to control metals
emissions.
(a) General. The owner or operator
must comply with the metals standards
provided by paragraphs (b), (c), (d), (e),
or (f) of this section for each metal listed
in paragraph (b) of this section that is
present in the hazardous waste at
detectable levels by using appropriate
analytical procedures.
*
*
*
*
*
I 39. Section 266.112 is amended by
revising paragraph (b)(1) introductory
text and paragraph (b)(2)(i) to read as
follows:
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§ 266.112
Regulation of residues.
*
*
*
*
*
(b) * * *
(1) Comparison of waste-derived
residue with normal residue. The wastederived residue must not contain
appendix VIII, part 261 constituents
(toxic constituents) that could
reasonably be attributable to the
hazardous waste at concentrations
significantly higher than in residue
generated without burning or processing
of hazardous waste, using the following
procedure. Toxic compounds that could
reasonably be attributable to burning or
processing the hazardous waste
(constituents of concern) include toxic
constituents in the hazardous waste,
and the organic compounds listed in
appendix VIII of this part that may be
generated as products of incomplete
combustion. For polychlorinated
dibenzo-p-dioxins and polychlorinated
dibenzo-furans, analyses must be
performed to determine specific
congeners and homologues, and the
results converted to 2,3,7,8-TCDD
equivalent values using the procedure
specified in section 4.0 of appendix IX
of this part.
*
*
*
*
*
(2) * * * (i) Nonmetal constituents:
The concentration of each nonmetal
toxic constituent of concern (specified
in paragraph (b)(1) of this section) in the
waste-derived residue must not exceed
the health-based level specified in
appendix VII of this part, or the level of
detection, whichever is higher. If a
health-based limit for a constituent of
concern is not listed in appendix VII of
this part, then a limit of 0.002
micrograms per kilogram or the level of
detection (which must be determined by
using appropriate analytical
procedures), whichever is higher, must
be used. The levels specified in
appendix VII of this part (and the
default level of 0.002 micrograms per
kilogram or the level of detection for
constituents as identified in Note 1 of
appendix VII of this chapter) are
administratively stayed under the
condition, for those constituents
specified in paragraph (b)(1) of this
section, that the owner or operator
complies with alternative levels defined
as the land disposal restriction limits
specified in § 268.43 of this chapter for
F039 nonwastewaters. In complying
with those alternative levels, if an
owner or operator is unable to detect a
constituent despite documenting use of
best good-faith efforts as defined by
applicable Agency guidance or
standards, the owner or operator is
deemed to be in compliance for that
constituent. Until new guidance or
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standards are developed, the owner or
operator may demonstrate such goodfaith efforts by achieving a detection
limit for the constituent that does not
exceed an order of magnitude above the
level provided by § 268.43 of this
chapter for F039 nonwastewaters. In
complying with the § 268.43 of this
chapter F039 nonwastewater levels for
polychlorinated dibenzo-p-dioxins and
polychlorinated dibenzo-furans,
analyses must be performed for total
hexachlorodibenzo-p-dioxins, total
hexachlorodibenzofurans, total
pentachlorodibenzo-p-dioxins, total
pentachlorodibenzofurans, total
tetrachlorodibenzo-p-dioxins, and total
tetrachlorodibenzofurans.
Note to this paragraph (b)(2)(i): The
administrative stay, under the condition that
the owner or operator complies with
alternative levels defined as the land disposal
restriction limits specified in § 268.43 of this
chapter for F039 nonwastewaters, remains in
effect until further administrative action is
taken and notice is published in the Federal
Register and the Code of Federal Regulations.
*
*
*
*
*
40. Appendix IX of part 266 is
amended to:
I a. Revise sections 1.0 and 3.0,
I b. Revise the first paragraph of section
4.0,
I c. Revise paragraph (2) of section 10.3,
I d. Revise the introductory text of the
fifth bullet of paragraph (1) of section
10.5,
I e. Revise the third dash text under the
second bullet of paragraph (2) of section
10.5,
I f. Revise the third and the introductory
text of the fifth bullet of paragraph (5) of
section 10.5,
I g. Revise the introductory text of the
fourth bullet of paragraph (1) of section
10.6,
I h. Revise the third and the
introductory text of the fourth bullet of
paragraph (5) of section 10.6.
The revisions read as follows:
I
Appendix IX to Part 266—Methods
Manual for Compliance With the BIF
Regulations
*
*
*
*
*
Section 1.0 Introduction
This document presents required methods
for demonstrating compliance with U.S.
Environmental Protection Agency regulations
for boilers and industrial furnaces (BIFs)
burning hazardous waste (see 40 CFR part
266, subpart H). The methods included in
this document are:
1. Performance Specifications for
Continuous Emission Monitoring (CEM) of
Carbon Monoxide, Oxygen, and
Hydrocarbons in Stack Gases.
2. Procedures for Estimating the Toxicity
Equivalency of Chlorinated Dibenzo-p-dioxin
and Dibenzofuran Congeners.
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3. Hazardous Waste Combustion Air
Quality Screening Procedures (HWCAQSP).
4. Simplified Land Use Classification
Procedure for Compliance with Tier I and
Tier II Limits.
5. Statistical Methodology for Bevill
Residue Determinations.
6. Procedures for Determining Default
Values for Air Pollution Control System
Removal Efficiencies.
7. Procedures for Determining Default
Values for Partitioning of Metals, Ash, and
Total Chloride/Chlorine.
8. Alternate Methodology for Implementing
Metals Controls.
a. Sampling and analytical methods for
multiple metals, hexavalent chromium, HCl
and chlorine, polychlorinated dibenzo-pdioxins and dibenzofurans, and aldehydes
and ketones can be found in ‘‘Test Methods
for Evaluating Solid Wastes, Physical/
Chemical Methods’’ (EPA Publication SW–
846). Additional methods referenced in
subpart H of part 266 but not included in this
document can be found in 40 CFR parts 60
and 61, and SW–846.
b. The CEM performance specifications of
section 2.0, the relevant sampling Methods
0011, 0023A, 0050, 0051, 0060, and 0061 of
SW–846, incorporated by reference in
§ 260.11, and the toxicity equivalency
procedure for dioxins and furans of section
4.0 are required procedures for determining
compliance with BIF regulations. For the
determination of chloride from HCl/Cl2
emission sampling train, you must use
appropriate methods. For the determination
of carbonyl compounds by high-performance
liquid chromatography, you must use
appropriate methods. The CEM performance
specifications are interim. The finalized CEM
performance specifications will be published
in 40 CFR parts 60 and 61.
*
*
Section 3.0
Methods
*
*
*
Sampling and Analytical
Note: The sampling and analytical methods
to the BIF manual are published in ‘‘Test
Methods for Evaluating Solid Waste,
Physical/Chemical Methods,’’ EPA
Publication SW–846.
Section 4.0 Procedure for Estimating the
Toxicity Equivalency of Chlorinated
Dibenzo-p-Dioxin and Dibenzofuran
Congeners
PCDDs and PCDFs must be determined
using whichever is the most recent version
between of SW–846 Method 0023A
(incorporated by reference, in § 260.11) as
identified, or OAQPS Method 23 of appendix
A to part 60. In this method, individual
congeners or homologues 1 are measured and
then summed to yield a total PCDD/PCDF
value. No toxicity factors are specified in the
method to compute risks from such
emissions.
*
*
*
*
*
term ‘‘congener’’ refers to any one
particular member of the same chemical
family; e.g., there are 75 congeners of
chlorinated dibenzo-p-dioxins. The term
‘‘homologue’’ refers to a group of structurally
related chemicals that have the same degree
of chlorination. For example, there are eight
homologues of CDs, monochlorinated
through octachlorinated. Dibenzo-p-dioxins
and dibenzofurans that are chlorinated at the
2,3,7, and 8 positions are denoted as ‘‘2378’’
congeners, except when 2,3,7,8–TCDD is
uniquely referred to: e.g., 1,2,3,7,8–PeCDF
and 2,3,4,7,8–PeCDF are both referred to as
‘‘2378–PeCDFs.’’
*
*
*
*
*
*
*
*
*
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*
10.3 Basis
*
*
*
(2) The metal concentrations in the
collected kiln dust can be accurately and
representatively measured.
*
*
*
*
*
10.5 Implementation Procedures
*
*
*
*
*
(1) * * *
• Follow appropriate guidelines for
preparing test plans and waste analysis plans
for the following tests:
*
*
*
*
*
(2) * * *
—Follow appropriate sampling and
analytical procedures such as those
described in the waste analysis plan as
they pertain to the condition and
accessibility of the dust.
*
*
*
*
*
(5) * * *
• Follow the sampling, compositing, and
analytical procedures described in this
method and in other appropriate methods, as
they pertain to the condition and
accessibility of the kiln dust. * * *
• Samples must be collected at least once
every 8 hours, and a daily composite must be
prepared according to appropriate
procedures.
*
*
*
*
*
10.6 Precompliance Procedures
*
*
*
*
*
(1) * * *
• Follow appropriate procedures for
preparing waste analysis plans for the
following tasks:
*
*
*
*
*
(5) * * *
• Follow the sampling, compositing, and
analytical procedures described in this
method and in other appropriate methods as
they pertain to the condition and
accessibility of the kiln dust.
• Samples must be collected at least once
every 8 hours, and a daily composite must be
prepared according to appropriate
procedures.
*
*
*
*
*
PART 268—LAND DISPOSAL
RESTRICTIONS
1 The
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41. The authority citation for part 268
continues to read as follows:
I
Authority: 42 U.S.C. 6905, 6912(a), 6921,
and 6924.
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Subpart D—Treatment Standards
42. Section 268.40 is amended by
revising paragraph (b) and footnote 7 of
the table ‘‘Treatment Standards for
Hazardous Wastes’’ to read as follows:
I
§ 268.40 Applicability of treatment
standards.
*
Section 10.0 Alternative Methodology for
Implementing Metals Controls
*
34589
*
*
*
*
(b) For wastewaters, compliance with
concentration level standards is based
on maximums for any one day, except
for D004 through D011 wastes for which
the previously promulgated treatment
standards based on grab samples remain
in effect. For all nonwastewaters,
compliance with concentration level
standards is based on grab sampling. For
wastes covered by the waste extract
standards, the test Method 1311, the
Toxicity Characteristic Leaching
Procedure found in ‘‘Test Methods for
Evaluating Solid Waste, Physical/
Chemical Methods,’’ EPA Publication
SW–846, as incorporated by reference in
§ 260.11, must be used to measure
compliance. An exception is made for
D004 and D008, for which either of two
test methods may be used: Method
1311, or Method 1310B, the Extraction
Procedure Toxicity Test. For wastes
covered by a technology standard, the
wastes may be land disposed after being
treated using that specified technology
or an equivalent treatment technology
approved by the Administrator under
the procedures set forth in § 268.42(b).
*
*
*
*
*
Treatment Standards for Hazardous
Wastes
*
*
*
*
*
7 Both
Cyanides (Total) and Cyanides
(Amenable) for nonwastewaters are to be
analyzed using Method 9010C or 9012B,
found in ‘‘Test Methods’ for Evaluating Solid
Waste, Physical/Chemical Methods,’’ EPA
Publication SW–846, as incorporated by
reference in 40 CFR 260.11, with a sample
size of 10 grams and a distillation time of one
hour and 15 minutes.
*
*
*
*
*
43. Section 268.44 is amended by
revising footnote 4 of the table ‘‘Wastes
Excluded From the Treatment Standards
Under § 268.40’’ to read as follows:
I
§ 268.44 Variance from a treatment
standard.
*
*
*
*
*
Table—Wastes Excluded From the
Treatment Standards Under § 268.40
*
*
*
(4)—Cyanide
*
*
nonwastewaters are analyzed
using SW–846 Method 9010C or 9012B, as
incorporated by reference in § 260.11 of this
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chapter, sample size 10 grams, distillation
time, 1 hour and 15 minutes.
which are present in the waste to be
burned, except that the applicant need
not analyze for constituents listed in
*
*
*
*
*
part 261, appendix VIII, of this chapter
I 44. Section 268.48 is amended by
which would reasonably not be
revising footnote 4 of the table
‘‘Universal Treatment Standards’’ to read expected to be found in the waste. The
constituents excluded from analysis
as follows:
must be identified and the basis for their
§ 268.48 Universal treatment standards.
exclusion stated. The waste analysis
*
*
*
*
*
must rely on appropriate analytical
techniques.
Universal Treatment Standards
(iv) An approximate quantification of
*
*
*
*
*
the hazardous constituents identified in
4 Both Cyanides (Total) and Cyanides the waste, within the precision
(Amenable) for nonwastewaters are to
produced by appropriate analytical
be analyzed using Method 9010C or
methods.
9012B, found in ‘‘Test Methods for
*
*
*
*
*
Evaluating Solid Waste, Physical/
I 48. Section 270.22 is amended by
Chemical Methods,’’ EPA Publication
revising paragraph (a)(2)(ii)(B) to read as
SW–846, as incorporated by reference in follows:
40 CFR 260.11, with a sample size of 10
§ 270.22 Specific part B information
grams and a distillation time of one
requirements for boilers and industrial
hour and 15 minutes.
furnaces burning hazardous waste.
*
*
*
*
*
*
*
*
*
*
I 45. Appendix IX to part 268 is revised
(a) * * *
as follows:
(2) * * *
(ii) * * *
Appendix IX to Part 268—Extraction
(B) Results of analyses of each waste
Procedure (EP) Toxicity Test Method
to be burned, documenting the
and Structural Integrity Test (Method
concentrations of nonmetal compounds
1310B)
listed in appendix VIII of part 261 of
this chapter, except for those
Note: The EP (Method 1310B) is published
in ‘‘Test Methods for Evaluating Solid Waste, constituents that would reasonably not
Physical/Chemical Methods,’’ EPA
be expected to be in the waste. The
Publication SW–846, as incorporated by
constituents excluded from analysis
reference in § 260.11 of this chapter.
must be identified and the basis for their
exclusion explained. The analysis must
PART 270—EPA ADMINISTERED
rely on appropriate analytical
PERMIT PROGRAMS: THE
techniques.
HAZARDOUS WASTE PERMIT
*
*
*
*
*
I
46. The authority citation for part 270
continues to read as follows:
§ 270.66 Permits for boilers and industrial
furnaces burning hazardous waste.
*
*
*
*
*
(c) * * *
(2) * * *
(i) An identification of any hazardous
organic constituents listed in appendix
VIII, part 261, of this chapter that are
present in the feed stream, except that
the applicant need not analyze for
constituents listed in appendix VIII that
would reasonably not be expected to be
found in the hazardous waste. The
constituents excluded from analysis
must be identified and the basis for this
exclusion explained. The waste analysis
must be conducted in accordance with
appropriate analytical techniques.
(ii) An approximate quantification of
the hazardous constituents identified in
the hazardous waste, within the
precision produced by appropriate
analytical methods.
*
*
*
*
*
Subpart F—Special Forms of Permits
Authority: 42 U.S.C. 6905, 6912, 6924,
6925, 6927, 6939, and 6974.
which would reasonably not be
expected to be found in the waste. The
constituents excluded from analysis
must be identified, and the basis for the
exclusion stated. The waste analysis
must rely on appropriate analytical
techniques.
(D) An approximate quantification of
the hazardous constituents identified in
the waste, within the precision
produced by appropriate analytical
methods.
*
*
*
*
*
I 50. Section 270.66 is amended by
revising paragraphs (c)(2)(i) and (ii) to
read as follows:
I
Subpart B—Permit Application
47. Section 270.19 is amended by
revising paragraphs (c)(1)(iii) and (iv) to
read as follows:
I
§ 270.19 Specific part B information
requirements for incinerators.
*
*
*
*
*
(c) * * *
(1) * * *
(iii) An identification of any
hazardous organic constituents listed in
part 261, appendix VIII, of this chapter,
PART 271—REQUIREMENTS FOR
AUTHORIZATION OF STATE
49. Section 270.62 is amended by
revising paragraphs (b)(2)(i)(C) and (D) to HAZARDOUS WASTE PROGRAMS
read as follows:
I 51. The authority citation for part 271
§ 270.62 Hazardous waste incinerator
continues to read as follows:
permits.
*
*
*
*
*
(b) * * *
(2) * * *
(i) * * *
(C) An identification of any hazardous
organic constituents listed in part 261,
appendix VIII of this chapter, which are
present in the waste to be burned,
except that the applicant need not
analyze for constituents listed in part
261, appendix VIII, of this chapter
Authority: 42 U.S.C. 6905, 6912(a) and
6926.
52. Section 271.1(j) is amended by
adding the following entries to Table 1
in chronological order by date of
publication in the Federal Register, to
read as follows:
I
§ 271.1
*
Purpose and scope.
*
*
(j) * * *
*
*
TABLE 1.—REGULATIONS IMPLEMENTING THE HAZARDOUS AND SOLID WASTE AMENDMENTS OF 1984
Promulgation date
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TABLE 1.—REGULATIONS IMPLEMENTING THE HAZARDOUS AND SOLID WASTE AMENDMENTS OF 1984—Continued
Promulgation date
Title of regulation
July 14, 2005 ..........................
July 14, 2005 ..........................
July 14, 2005 ..........................
Federal Register reference
*
*
*
*
*
Process Vent and Equipment Leak Organic Air Emission
Standards for Owners and of Operators of Hazardous
Waste Treatment, Storage, and Disposal Facilities.
Burning of Hazardous Waste in Boilers and Industrial Furnaces.
Air Emission Standards Tanks, Surface Impoundments,
Containers.
*
*
*
*
*
I 53. Section 271.21 is amended by
adding the following entries to Table 1
*
*
[Insert FR page citation of
publication date].
July 14, 2005.
[Insert FR page citation of
publication date].
[Insert FR page citation of
publication date].
in chronological order by date of
publication in the Federal Register, to
read as follows:
Effective date
July 14, 2005.
July 14, 2005.
§ 271.21 Procedures for revision of State
programs.
*
*
*
*
*
TABLE 1 TO § 271.21
Title of regulation
Promulgation date
*
*
*
*
Office of Solid Waste Testing and Monitoring Activities, Methods Innovation
Rule.
Process Vent and Equipment Leak Organic Air Emission Standards for
Owners and Operators of Hazardous Waste Treatment, Storage, and
Disposal Facilities.
Burning of hazardous waste in boilers and industrial furnaces .....................
*
*
*
July 14, 2005 .....................................
July 14, 2005 .....................................
Air Emissions Standards for Tanks, Surface Impoundments, and Containers.
July 14, 2005 .....................................
PART 279—STANDARDS FOR THE
MANAGEMENT OF USED OIL
54. The authority citation for part 279
continues to read as follows:
I
Authority: Sections 1006, 2002(a), 3001
through 3007, 3010, 3014, and 7004 of the
Solid Waste Disposal Act, as amended (42
U.S.C. 6905, 6912(a), 6921 through 6927,
6930, 6934, and 6974); and sections 101(37)
and 114(c) of CERCLA (42 U.S.C. 9601(37)
and 9614(c)).
Subpart B—Applicability
55. Section 279.10 is amended by
revising paragraph (b)(1)(ii) introductory
text to read as follows:
I
§ 279.10
Applicability.
*
*
*
*
*
(b) * * *
(1) * * *
(ii) Rebuttable presumption for used
oil. Used oil containing more than 1,000
ppm total halogens is presumed to be a
hazardous waste because it has been
mixed with halogenated hazardous
waste listed in subpart D of part 261 of
this chapter. Persons may rebut this
presumption by demonstrating that the
used oil does not contain hazardous
waste (for example, by showing that the
used oil does not contain significant
concentrations of halogenated
hazardous constituents listed in
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July 14, 2005 .....................................
appendix VIII of part 261 of this
chapter).
*
*
*
*
*
[Insert FR page citation of
publication date].
[Insert FR page citation of
publication date].
[Insert FR page citation of
publication date].
[Insert FR page citation of
publication date].
Subpart F—Standards for Used Oil
Processors and Re-Refiners
57. Section 279.53 is amended by
revising paragraph (c) introductory text
to read as follows:
I
Subpart E—Standards for Used Oil
Transporter and Transfer Facilities
56. Section 279.44 is amended by
revising the introductory text of
paragraph (c) to read as follows:
I
§ 279.44
oil.
Rebuttable presumption for used
*
*
*
*
*
(c) If the used oil contains greater than
or equal to 1,000 ppm total halogens, it
is presumed to be a hazardous waste
because it has been mixed with
halogenated hazardous waste listed in
subpart D of part 261 of this chapter.
The owner or operator may rebut the
presumption by demonstrating that the
used oil does not contain hazardous
waste (for example, by showing that the
used oil does not contain significant
concentrations of halogenated
hazardous constituents listed in
appendix VIII of part 261 of this
chapter).
*
*
*
*
*
PO 00000
§ 279.53
oil.
Rebuttable presumption for used
*
*
*
*
*
(c) If the used oil contains greater than
or equal to 1,000 ppm total halogens, it
is presumed to be a hazardous waste
because it has been mixed with
halogenated hazardous waste listed in
subpart D of part 261 of this chapter.
The owner or operator may rebut the
presumption by demonstrating that the
used oil does not contain hazardous
waste (for example, by showing that the
used oil does not contain significant
concentrations of halogenated
hazardous constituents listed in
appendix VIII of part 261 of this
chapter).
*
*
*
*
*
Subpart G—Standards for Used Oil
Burners Who Burn Off-Specification
Used Oil for Energy Recovery
58. Section 279.63 is amended by
revising paragraph (c) introductory text
to read as follows:
I
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Rebuttable presumption for used
*
*
*
*
*
(c) If the used oil contains greater than
or equal to 1,000 ppm total halogens, it
is presumed to be a hazardous waste
because it has been mixed with
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halogenated hazardous waste listed in
subpart D of part 261 of this chapter.
The owner or operator may rebut the
presumption by demonstrating that the
used oil does not contain hazardous
waste (for example, by showing that the
used oil does not contain significant
PO 00000
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concentrations of halogenated
hazardous constituents listed in
appendix VIII of part 261 of this
chapter).
*
*
*
*
*
[FR Doc. 05–10197 Filed 6–13–05; 8:45 am]
BILLING CODE 6560–50–P
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Agencies
[Federal Register Volume 70, Number 113 (Tuesday, June 14, 2005)]
[Rules and Regulations]
[Pages 34538-34592]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-10197]
[[Page 34537]]
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Part II
Environmental Protection Agency
-----------------------------------------------------------------------
40 CFR Parts 63, 268, et al.
Waste Management System; Testing and Monitoring Activities; Final Rule:
Methods Innovation Rule and SW-846 Final Update IIIB; Final Rule
Federal Register / Vol. 70, No. 113 / Tuesday, June 14, 2005 / Rules
and Regulations
[[Page 34538]]
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
40 CFR Parts 63, 258, 260, 261, 264, 265, 266, 268, 270, 271, and
279
[RCRA-2002-0025; FRL-7916-1]
RIN 2050-AE41
Waste Management System; Testing and Monitoring Activities; Final
Rule: Methods Innovation Rule and SW-846 Final Update IIIB
AGENCY: Environmental Protection Agency (EPA).
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: The Environmental Protection Agency is amending a variety of
testing and monitoring requirements in the Resource Conservation and
Recovery Act (RCRA) hazardous and non-hazardous solid waste regulations
and for certain Clean Air Act (CAA) regulations that relate to
hazardous waste combustors. These amendments allow more flexibility
when conducting RCRA-related sampling and analysis by removing from the
regulations a requirement to use the methods found in ``Test Methods
for Evaluating Solid Waste, Physical/Chemical Methods,'' also known as
``SW-846,'' in conducting various testing and monitoring and by
limiting required uses of an SW-846 method to circumstances where the
method is the only one capable of measuring the particular property
(i.e., the method is used to measure a required method-defined
parameter). This action is an important step forward in implementing
the use of a performance-based approach, which is part of the Agency's
efforts toward Innovating for Better Environmental Results.
Additionally, the Agency is making certain other clarifications and
technical amendments. These changes should make it easier and more cost
effective to comply with the affected regulations, without compromising
human health or environmental protection.
DATES: This final rule is effective on July 14, 2005. The incorporation
by reference of certain publications listed in the rule is approved by
the Director of the Federal Register as of July 14, 2005.
ADDRESSES: EPA has established a docket for this action under Docket ID
No. RCRA-2002-0025. All documents in the docket are listed in the
EDOCKET index at https://www.epa.gov/edocket. Although listed in the
index, some information is not publicly available, i.e., CBI or other
information for which disclosure is restricted by statute. Certain
other material, such as copyrighted material, is not placed on the
Internet and will be publicly available only in hard copy form.
Publicly available docket materials are available either electronically
in EDOCKET or in hard copy at the OSWER RCRA Docket, EPA/DC, EPA West,
Room B102, 1301 Constitution Ave., NW., Washington, DC. The Public
Reading Room is open from 8:30 a.m. to 4:30 p.m., Monday through
Friday, excluding legal holidays. The telephone number for the Public
Reading Room is (202) 566-1744. This Docket Facility is open from 8:30
a.m. to 4:30 p.m., Monday through Friday, excluding legal holidays. The
Docket telephone number is (202) 566-0270.
FOR FURTHER INFORMATION CONTACT: For information on this rulemaking,
contact Kim Kirkland at: Office of Solid Waste (5307W), U. S.
Environmental Protection Agency, 1200 Pennsylvania Avenue, SW.,
Washington, DC 20460-0002, (703) 308-8855, e-mail address:
kirkland.kim@epa.gov.
SUPPLEMENTARY INFORMATION:
I. General Information
A. Does This Action Apply to Me?
You may be covered by this action if you conduct waste sampling and
analysis for Resource Conservation and Recovery Act (RCRA)-or National
Emission Standards for Hazardous Air Pollutants (NESHAP)-related
activities. Covered entities include anyone who generates, treats,
stores, or disposes of hazardous or nonhazardous solid waste and is
subject to RCRA subtitle C or D sampling and analysis requirements; and
entities subject to NESHAP final standards for hazardous waste
combustors (40 CFR part 63, subpart EEE). All types of industries,
governments, and organizations may have entities that generate or
manage RCRA-regulated hazardous and nonhazardous solid wastes and may
be subject to RCRA-related sampling and analysis requirements.
To determine whether your facility, company, business organization,
etc., is covered by this action, you should carefully examine the
applicability criteria in part 63 and in parts 258 through 299 of the
Code of Federal Regulations. If you have questions regarding the
applicability of this action to a particular entity, consult your
regulatory authority.
B. How Do I Obtain Copies of SW-846?
The Third Edition of SW-846, as amended by Final Updates I, II,
IIA, IIB, III, IIIA, and IIIB will be available in pdf format on the
Internet at https://www.epa.gov/SW-846. A paper copy of Final Update
IIIB is also located in the docket for this rule (see section I.A
above). Table 1 below provides sources for both paper and electronic
copies of the Third Edition of SW-846 and all of its updates.
Table 1.--Sources for SW-846, Third Edition, and its Updates
------------------------------------------------------------------------
Source Available portions of SW-846
------------------------------------------------------------------------
Superintendent of Documents, --Paper copies of the SW-846, Third
U.S. Government Printing Edition, basic manual and of certain
Office (GPO), Washington, DC updates, including Final Updates, I,
20402, phone (202) 512-1800, II, IIA, IIB, III, and IIIB and Draft
toll free (866) 512-1800, fax Update IVA. The subscriber must
orders (202) 512-2250, and integrate the updates.
online: https://
bookstore.gpo.gov.
National Technical Information --Paper copy of an integrated version of
Service (NTIS), 5285 Port SW-846, Third Edition, as amended by
Royal Road, Springfield, VA Final Updates, I, II, IIA, IIB, III,
22161, (703) 605-6000 or and IIIA.
(800) 553-6847. --Individual paper copies of the SW-846,
Third Edition, basic manual and of
certain updates, including Final
Updates I, II, IIA, IIB, III, IIIA, and
IIIB and Draft Updates IVA and IVB.
--CD-ROM of integrated version of SW-
846, Third Edition, as amended by Final
Updates I, II, IIA, IIB, and III (pdf
and WordPerfect electronic copies).
--CD-ROM of Draft Update IVA (pdf and
WordPerfect electronic copies).
Internet: https://www.epa.gov/ --Integrated version of SW-846, Third
SW-846. Edition, as amended by Final Updates I,
II, IIA, IIB, III, IIIA, and IIB (pdf
electronic copy).
--Draft Update IVA (pdf electronic
copy).
--Draft Update IVB (pdf electronic
copy).
------------------------------------------------------------------------
[[Page 34539]]
C. What Is the Legal Authority for This Action?
We are promulgating the part 258, 260, 261, 264-266, 268, 270, 271,
and 279 regulations under the authority of sections 1006, 2002(a),
3001-3007, 3010, 3013-3018, and 7004 of the Solid Waste Disposal Act,
as amended by the Resource Conservation and Recovery Act of 1976, as
amended. We are promulgating the part 63 regulation under the authority
of sections 112 and 114 of the Clean Air Act.
D. How Is the Rest of This Preamble Organized?
II. Summary of Today's Rule
III. Background and Purpose of Action To Reform RCRA-Related Testing
and Monitoring
A. Public Comments Regarding How to Determine if a Method Is
Appropriate
B. Public Comments Regarding Other Approaches
C. Public Comments Regarding Impacts From Removal of Required
Uses of SW-846 Methods
IV. Regulatory Revisions Involving Removal of SW-846 Requirements
V. Editorial Corrections to SW-846 References in the RCRA Testing
and Monitoring Regulations
VI. Action to Withdraw the Reactivity Interim Guidance from SW-846
Chapter Seven and Remove Required SW-846 Reactivity Analyses and
Threshold Levels from Conditional Delistings
VII. Clarifications to Corrosivity and Ignitability Hazardous Waste
Characteristics
A. Revision to Sec. 261.22(a)(2) to Clarify that SW-846 Method
1110A Is the SW-846 Standardized Version of the NACE Standard
Specified for Corrosivity Characteristic Testing
B. Revisions to Sec. 261.21(a)(1) to Remove an Unnecessary
Referral to Method Equivalency Petitions; and an Explanation
regarding the Decision to Not Revise the Regulation to Include the
Updated ASTM Standards and References to Methods 1010A and 1020B as
Proposed
VIII. Availability of Final Update IIIB and Status of Final Update
IV to SW-846
IX. Addition of Method 25A to Sec. Sec. 264.1034(c)(1)(ii) and (iv)
and 265.1034(c)(1)(ii) and (iv)
X. Removal of Requirements from Sec. 63.1208(b)(8)(i) and (ii) in
the NESHAP Standards to Demonstrate Feedstream Analytes Are Not
Present at Certain Levels
XI. Status of the RCRA Waste Sampling Draft Technical Guidance
XII. State Authorization Procedures
A. Applicability of Federal Rules in Authorized States
B. Authorization of States for Today's Rule
C. Abbreviated Authorization Procedures
XIII. Statutory and Executive Order Reviews
A. Executive Order 12866: Regulatory Planning and Review
B. Paperwork Reduction Act
C. Regulatory Flexibility Act
D. Unfunded Mandates Reform Act
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
J. Executive Order 12898: Federal Actions to Address
Environmental Justice in Minority Populations and Low-Income
Populations
K. Congressional Review Act
II. Summary of Today's Rule
On October 30, 2002 (67 FR 66251-66301), the Environmental
Protection Agency (EPA) proposed to amend the testing and monitoring
requirements under the hazardous and nonhazardous solid waste
regulations, and a testing requirement under the Clean Air Act (CAA) in
the National Emission Standards for Hazardous Air Pollutants (NESHAP)
for hazardous waste combustors. EPA is finalizing those regulatory
revisions at this time. Some of the public comments are summarized and
addressed in the sections to follow, and a background document
containing our responses to all public comments can be found in the
docket to this rule, RCRA-2002-0025. After consideration of all
comments and for the reasons summarized in today's rule, we are
finalizing the following actions:
1. Reforming RCRA-related testing and monitoring by restricting
requirements to use SW-846 to only those situations where the method is
the only one capable of measuring the property (i.e., it is used to
measure a method-defined parameter). This will allow more flexibility
in RCRA-related sampling and analysis by removing unnecessary required
uses of SW-846.
2. Withdrawing the cyanide and sulfide reactivity guidance from
sections 7.3.3 and 7.3.4 of SW-846 Chapter Seven and withdrawing
required uses of reactive cyanide and sulfide methods and threshold
levels from conditional delistings.
3. Amending the regulations for the ignitability and corrosivity
hazardous waste characteristics. As part of this, we are clarifying in
Sec. 261.22(a)(2) that SW-846 Method 1110A, ``Corrosivity Toward
Steel,'' is the ``standardized'' (as described in Sec. 261.22(a)(2))
SW-846 method that is required to be used to determine the
characteristic of corrosivity for steel. We are also removing the
unnecessary reference to equivalency petitions in the ignitability
characteristic at Sec. 261.21(a)(1). However, regarding the methods
required for the determination of flash point under the characteristic
of ignitability, the Agency decided not to replace the standard test
methods ASTM D 3278-78 and D 93-79 with the latest versions of those
methods.
4. Incorporating by reference Update IIIB to SW-846, which includes
the revised Chapter Seven, and eleven revised methods, including method
revisions to remove a requirement to use the SW-846 Chapter Nine,
``Sampling Plan.''
5. Adding Method 25A as an analytical option to analyses conducted
in support of air emission standards for process vents and/or equipment
leaks at treatment, storage, and disposal facilities.
6. Removing a requirement to demonstrate that feedstream analytes
are not present at levels above the 80% upper confidence limit above
the mean for sources subject to NESHAP: Final Standards for Hazardous
Waste Combustors.
7. Removing from the regulations unnecessary references to SW-846,
which do not affect the intent of the RCRA regulation.
This rule does not add any additional requirements to the
regulations. Instead, this rule removes the requirement to use SW-846,
and it clarifies what the Agency believes should be considered during
the selection of other appropriate methods. Our purpose for the
regulatory revisions is to make it easier and more cost effective to
comply with the RCRA regulations by allowing more flexibility in method
selection and use. If you prefer, where you find that a specific SW-846
method yields data that is suitably effective for demonstrating
compliance in the particular matrix being analyzed, you can still use
the SW-846 methods.
III. Background and Purpose of Action to Reform RCRA-Related Testing
and Monitoring
Typically, the hazardous and nonhazardous solid waste RCRA
regulations for testing and monitoring activities or the permits or
waste analysis plans of facilities regulated by RCRA specify the
analytes of concern to be determined in a matrix of concern at a
particular regulatory level of concern. Additionally, some recently
promulgated regulations specify the confidence level of concern. Most
of the RCRA regulations leave the how (i.e., which test method to use)
up to the regulated community. Some RCRA regulations, however, specify
the use of methods from the EPA publication
[[Page 34540]]
``Test Methods for Evaluating Solid Waste, Physical/Chemical Methods,''
also known as ``SW-846.''
Initially, EPA issued SW-846 in 1980 soon after the first RCRA
regulations were published. At that time, we intended that SW-846 serve
two roles. First, the Agency intended that it serve as a guidance
manual of generally appropriate and reliable analytical methods for
RCRA-related testing and monitoring. Second, we intended that it serve
as a readily-available source of those few analytical methods which
were required in order to comply with the RCRA regulations. Since that
time, EPA published regulations that required the use of SW-846 methods
in general. Subsequently, members of the regulated public made it clear
to EPA that they would like the opportunity to use other reliable
methods, and EPA also decided that some of the SW-846 requirements were
not necessary.
The regulatory requirement to use SW-846 in general (e.g., as in
the delisting regulations at Sec. 260.22 prior to this final rule) did
not identify specific SW-846 methods. Rather, this requirement
typically included the regulation of many different analytes which
could be determined by many different methods. Almost every update to
SW-846 includes at least one method that may be applicable to one or
more of these general analytical requirements. Therefore, whenever SW-
846 was updated to revise or add methods, EPA had to incorporate by
reference all of the new and revised methods into the RCRA regulations
as part of a rulemaking. EPA issued the updates as a proposed rule,
requested public comment, and then promulgated the update in a final
rule. This lengthy process delayed the timely use of the new analytical
technologies.
On October 30, 2002 (67 FR 66251-66301), EPA proposed to remove
from the regulations a requirement to use a method found in SW-846,
except when that method is the only one capable of measuring the
particular property. At that time, we described our reasons for wanting
to remove this requirement from the regulations, including the Agency's
desire to fully implement a performance-based measurement system (PBMS)
in the RCRA program. Specifically, we noted that such a change would:
(1) Allow the regulated community more flexibility in method use during
RCRA-required testing; (2) stimulate the development and timely use of
innovative and more cost-effective monitoring technologies and
approaches in the RCRA program; (3) allow more efficient and timely
releases of SW-846 methods by decoupling most of the methods from
required uses in the RCRA regulations; and (4) make the RCRA program
more effective by focusing on measurement objectives rather than on
measurement technologies. As noted, the Agency proposed to restrict the
requirement to use a specific SW-846 method to only those situations
where its particular procedure is the only one that is capable of
measuring the property (i.e., a method-defined parameter, or MDP). For
example, to determine whether the levels of hazardous constituents in a
particular waste stream are equal to or greater than the toxicity
characteristic (TC) levels specified in Sec. 261.24, waste generators
must test their waste using SW-846 Method 1311, the ``Toxicity
Characteristic Leaching Procedure,'' or ``TCLP.'' If levels in the
waste are greater than or equal to the TC levels, the waste is a
hazardous waste and is subject to the RCRA hazardous waste regulations.
This is the only reliable method for determining whether TC levels are
met. Thus, testing of any material to determine whether it meets the
Toxicity Characteristic levels must be done using the TCLP. EPA
describes the measurement obtained from the TCLP, as well as from
certain other methods, as a required ``method-defined parameter.''
We requested public comment on the proposed revisions to the RCRA
regulations, although not to the method-defined parameters, and
received comments on the proposed action from over 20 different
commenters, which included representatives of Federal Government
agencies, State Government agencies, industry, waste generation and
management entities, and analytical laboratories. The majority (86%) of
the commenters generally supported, with comment, the MIR action and
EPA's efforts to allow more flexibility in method selection when
conducting RCRA-related sampling and analysis. Regarding the positive
comments, one commenter, a state agency representative, applauded EPA
for recognizing that regulating does not have to be prescriptive.
Another commenter, a representative of analytical laboratories,
believed that the additional flexibility will result in data quality
improvements. Two representatives of waste generation or management
entities concurred with EPA that the majority of the MIR revisions
should make it easier and more cost effective to comply with RCRA-
related regulations.
For the most part, the negative public comments may have reflected
a misunderstanding of certain important aspects and premises of the
MIR, which we are clarifying in our responses to those comments. With
respect to other negative comments, the Agency expects that the
discussion below will further clarify the purposes and premises of the
MIR, and will clarify options for dealing with the inherent flexibility
of this approach. Also, the Agency will continue to provide training on
the concepts of this rule to further clarify its intent and support its
implementation. You will find a background document containing our
complete responses to all relevant public comments in the docket to
this rule, docket number RCRA-2002-0025, at the location listed above
under ADDRESSES. Some of the public comments are also addressed within
this preamble to the final rule.
Based on our review of the public comments regarding the October
30, 2002 proposed rule, we are proceeding with publication of this
final rule, which finalizes the proposed revisions to the RCRA
regulations. That is, this rule removes unnecessary required uses of
SW-846 in general and it removes any unnecessary required uses of
specific SW-846 methods. Other reliable methods can now be used by the
regulated public for compliance with the affected regulations. This
action also encourages the timely use of new and innovative methods
outside of SW-846 in that, for most sampling and analysis scenarios, it
will not be necessary to submit an equivalency petition when using a
non-SW-846 method. However, some regulations will still require use of
a specific SW-846 method when that method is for determination of a
RCRA-required method-defined parameter (MDP); in those cases, a
regulated entity has to submit an equivalency petition and receive
approval of that petition from the Agency before an alternative method
can be used.
This final rule will allow the Agency to make final updates to SW-
846 available in a more timely manner. For example, soon after
publication of this document, we will announce the availability of
Final Update IV (see section VIII of this document). The methods of
Final Update IV did not have to go through the rulemaking process
because, with publication of this final rule, SW-846 is no longer
required in general by any existing RCRA regulation and none of the new
or revised methods in Update IV are specifically required by any RCRA
regulation for the analysis of method-defined parameters (MDPs).
However, we did solicit and consider public comments on the methods
through Federal Register notices, see 63 FR 25430-25438, May 8, 1998
(Draft
[[Page 34541]]
Update IVA), and 65 FR 70678-70681, November 27, 2000 (Draft Update
IVB).
A. Public Comments Regarding How To Determine if a Method Is
Appropriate
In section III.A of the preamble to the October 30, 2002 proposed
rule, we discussed our proposed revisions to remove the requirement to
use SW-846 methods by adding regulatory language allowing the use of
appropriate methods such as those found in SW-846 or other reliable
sources. In the preamble of the proposed rule, we provided guidance on
how to determine if a method is appropriate for its analytical purpose.
Specifically, we mentioned that such a method might be one published by
EPA in a different manual or regulation or published by another
government agency, a voluntary standards setting organization, or other
well-known sources. We also proposed to retain mention of the SW-846
methods in the regulations as guidance and as examples of methods that
could be appropriate.
In the proposed rule preamble, we gave two primary considerations
in selecting an appropriate method, which together serve as our general
definition of an appropriate method. As done in the preamble to the
proposed rule, the text to follow explains each of these concepts and
identifies other guidance that may be helpful to the regulated
community.
1. Appropriate methods are reliable and accepted as such in the
scientific community.
2. Appropriate methods generate effective data.
Regarding the first consideration, we noted that methods which are
reliable and accepted in the scientific community might include those
published by the Agency or other government entities using techniques
that have documented reliability. SW-846 methods, for example, are
reviewed by a technical workgroup composed of national expert-level
chemists who provide peer input and determine whether method
reliability is sufficiently documented. The technical reliability and
acceptance of other methods published by other governmental or non-
governmental organizations may also be documented, especially if the
methods are subjected to some form of objective scientific review. For
instance, to qualify for recognition as having developed a voluntary
consensus standard (e.g., analytical method) under the National
Technology Transfer & Advancement Act of 1995 (NTTAA), an organization
must produce standards by consensus, observe the principles of openness
and balance of interests, and provide due process, including an appeals
process.
Regarding the second consideration in the identification of
appropriate methods--generation of effective data--we described in the
preamble to the proposed rule examples of tools that might be used in
this determination. This consideration is project-specific and
therefore the tools and criteria will be different for each analytical
effort. As stated in the proposed rule preamble, effective data are
data of sufficiently known and appropriate quality to be used in making
project-specific decisions. An example of such a decision is whether a
particular waste is hazardous because a constituent of concern is
present above a level of concern. Before sampling and analysis begins,
project planners should identify why the analysis is being done, how
the data will be used, and how ``good'' the data has to be (e.g., the
quality objectives for the project as established through a systematic
planning process). Effective data meet the quality objectives set by
the project planners for the specific project. The quality objectives
should be rationally and systematically identified during the planning
of the project and development of the project-specific Quality
Assurance Project Plan (QAPP), Waste Analysis Plan (WAP), Sampling and
Analysis Plan (SAP), or other appropriate systematic planning document.
Sampling and analysis documentation should be sufficient to confirm
that the data are effective and that the selected method is
appropriate.
Quality objectives generally refer to the necessary quality of the
overall decision to be made or, in other words, the tolerable error
(i.e., acceptable level of uncertainty for the decision). For example,
a quality objective for waste analysis may be that one must demonstrate
that an analyte is not present above the reported level at the 80
percent upper confidence around the mean, and that the method could
have detected the presence of the analyte at that level and confidence
limit. A quality objective may be specified in a regulation, a permit,
a corrective action agreement, or other regulatory or enforcement
document. Sometimes you must consider a quality objective regulatory
specification when selecting an appropriate method. For example, the
RCRA comparable fuels' provisions include quality objectives in lieu of
naming the use of specific methods (see 63 FR 33781, June 19, 1998).
You can find guidance on the development of formal data quality
objectives (DQOs) in EPA's ``Guidance for the Data Quality Objectives
Process'' (EPA QA/G-4) found at EPA's Quality Staff's Web site (https://
www.epa.gov/quality/), in Chapter One, ``Quality Control,'' of SW-846,
and in ASTM D 5792, ``Standard Practice for Generation of Environmental
Data Related to Waste Management Activities: Development of Data
Quality Objectives.'' You may also use other scientifically valid
systematic planning processes for developing quality objectives based
on specific project needs.
In the project planning document, you should identify the types of
quality control (QC) concepts (e.g., spike recovery analyses, blanks,
etc.) you will use to determine if you meet your objectives. For
example, selection of an appropriate method is sometimes demonstrated
by adequate recovery of spiked or surrogate analytes and reproducible
results, or through successful analysis of a standard reference
material of a matrix-type analogous to that of the actual sample
matrix. The method may not be appropriate for its intended use if your
data show inadequate recovery of an analyte at a level that impairs a
decision regarding whether the analyte is present at or below its
regulatory level. Such a method would not generate effective data.
Based on your QC data, you should determine whether the method
generates results that are sufficiently sensitive, unbiased, and
precise to demonstrate compliance with the subject regulation.
However, you should not just focus on controlling or documenting
analytical quality, because regulatory decisions are also susceptible
to error due to sampling procedures. If the contaminant variability is
not properly addressed during the planning and collection of samples,
an incorrect decision could be reached even though the method performed
well in terms of laboratory quality control. No matter how accurate or
precise the laboratory analysis, the data will provide misleading
information if excessive error is introduced by improper sampling
procedures. Guidance on identifying the necessary quality control
procedures and on minimizing the potential for both analytical and
sampling error can be found at the EPA Quality Staff's Web site (http:/
/www.epa.gov/quality/) or in Chapters One, Two, and Nine of SW-846. In
addition, guidance on determining and demonstrating the appropriateness
of a selected measurement method for a particular application may be
found in ASTM D 6956-03, ``Standard Guide for Demonstrating and
Assessing Whether a Chemical Analytical Measurement
[[Page 34542]]
System Provides Analytical Results Consistent with Their Intended
Use.''
Finally, EPA noted in the proposed rule preamble that you should
identify appropriate methods for a specific project before sampling and
analysis begins. As the regulated entity, you are ultimately
responsible for compliance with a particular regulation. Therefore, you
should not rely on the laboratory or other project participant to
select an appropriate method. We recommend that you consult with your
regulating authority during identification of performance goals and the
selection of appropriate methods.
We requested and received public comment on the above
considerations and on the proposal to allow the use of appropriate
methods such as those found in SW-846 or other reliable sources. One
supportive commenter believed the Agency had provided sufficient
guidance in the preamble to the proposed rule on how to identify
appropriate methods. As discussed below, a few commenters requested
additional guidance regarding the selection of appropriate methods or
had questions regarding the approach.
One commenter requested that an appropriate method definition be
codified in the regulations. The Agency believes that codification of
an appropriate method definition would be both very difficult and
contrary to the intent and purpose of this rule, given the project-
specific nature of ``appropriate method selection'' and the wide
variety of data collection objectives that may be encountered. In the
paragraphs above, the Agency has provided the key generic
considerations for appropriate method selection, which together serve
as our general definition for an appropriate method, and identified
guidance sources, in the hope that this information will assist readers
of this rule during the selection of appropriate methods, regardless of
whether the methods are from SW-846 or other sources. In addition,
since publication of the proposed rule, ASTM International published D
6956-03, ``Standard Guide for Demonstrating and Assessing Whether a
Chemical Analytical Measurement System Provides Analytical Results
Consistent with Their Intended Use.'' This guidance document is not
required by any EPA program, but may be useful to the regulated
community during the selection of appropriate methods and during the
evaluation of analytical results. The document can be obtained from
ASTM by visiting its Web site at https://www.ASTM.org or by writing to:
ASTM International, 100 Barr Harbor Drive, P.O. Box C700, West
Conshohocken, PA 19418-2959. EPA also plans to continue to provide
training to affected entities on the concepts of this rule and to
support its implementation. When using any appropriate method, you
should be able to determine the analyte of concern (e.g., the regulated
constituent to be measured), in the matrix of concern (e.g., the
physical substance which might contain the regulated constituent), at
the level of concern (e.g., the regulated level of or the action level
for the analyte).
One commenter was concerned that the regulated public might use
other methods that do not meet the QC criteria in the SW-846 methods.
The Agency does not believe that this should be a concern. The
performance data and QC criteria given in the SW-846 methods are only
examples, and are not requirements for analysis. The SW-846 example
criteria may not be appropriate for every analytical purpose.
Establishing QC criteria is a project planning issue and not a method
issue. Methods should be adapted into standard operating procedures
(SOPs) to meet QC criteria from systematic planning documents, not the
other way around. Some analytical applications may require more or less
stringent QC criteria than that given as examples in the SW-846
methods, and it would be contrary to promoting a PBMS approach if all
analyses using any methods are expected to conform to the example
criteria published in SW-846 methods. Sometimes, even when using an SW-
846 method, it may not be necessary to fully meet its example
performance criteria because project-specific quality objectives may
not require evaluation of the same performance indicators or the
criteria may not be appropriate to the specific application. In keeping
with a PBMS approach and the goals of this rule, performance criteria
should be determined on a project-specific basis during the planning
stage.
Another commenter was concerned that some regulated entities might
use methods that were not originally developed for environmental
purposes, and thus data validity may be suspect. Provided that the
method is appropriate based on the factors discussed above and in the
proposed rule preamble, we do not believe that this should be a
concern. If the data are suspect or otherwise not of sufficient quality
for their intended use, then the method is not appropriate, regardless
of its source, and thus the data are not acceptable for demonstrating
compliance. Regardless of the original purpose or source of a method,
it can be an appropriate method if it generates effective data, e.g.,
the data quality objectives and performance criteria are met. Even an
SW-846 method may not be appropriate for a particular application if it
does not generate effective data. In addition, the application of
method technologies from other disciplines promotes the use of
innovative approaches and technologies, which may benefit RCRA-related
analyses. Finally, many of the analytical techniques used today in
environmental analyses were initially developed for other purposes.
One commenter agreed with EPA's approach to appropriate method
selection, but had comments regarding the data quality objectives
approach. The commenter believed that the DQO approach can be expensive
and is not usually used during small analytical projects. In response,
the Agency notes that, when data are being used in decision making
involving two clearly alternative conditions (e.g., compliance vs.
noncompliance with a regulatory standard), the Agency's recommended
systematic planning tool is the DQO process. While there is no
regulatory obligation to use the DQO process, it is the recommended
planning approach for many EPA data collection activities. However, the
DQO process may be too complicated for some projects and is not the
only way to generate quality data through systematic planning. It is
presented here in the MIR only as an example of an approach involving
systematic planning. However, at a minimum, the Agency recommends that
some form of systematic planning be implemented for every data
collection effort in order to generate effective data, and notes that
such systematic planning should also involve consideration of cost.
Systematic planning is a common sense approach, designed to ensure that
the level of detail in planning is commensurate with the importance and
intended use of the work and the available resources.
One commenter supported EPA's proposed flexibility, but thought
that EPA should continue to use SW-846 as the primary vehicle for
making recommendations regarding procedures that will meet minimum
quality objectives for RCRA analyses. Thus, one would not be required
to use SW-846 methods, but could choose to use them and be confident
that they are appropriate sampling and analysis procedures, provided
that they can be demonstrated to meet project quality objectives.
Another commenter believed that it would be unrealistic for a regulated
entity to agree to the use of other methods if EPA has not approved
them. The commenter believed that such approval would guarantee
[[Page 34543]]
acceptance of the data, provided that the method was properly followed.
First, it should be noted that there are no ``PBMS methods.'' PBMS
is a regulatory approach where what has to be accomplished is
specified, rather than how the monitoring is to be conducted. Under
such a system, regulated entities are permitted to employ any method
that is technically adequate to accomplish the compliance
demonstration. Regarding EPA's approval of PBMS, EPA has already stated
its objective to employ the performance approach in its regulatory and
other monitoring programs to the extent feasible. On October 6, 1997
(62 FR 52098-52100), EPA published in the Federal Register its intent
to adopt PBMS agency-wide. Subsequently, on May 8, 1998 (63 FR 25430-
25438), EPA published in the Federal Register a notice of intent and
request for comment regarding its plans to reform implementation of
RCRA-related monitoring by formally adopting PBMS and by removing
unnecessary required uses of methods from the RCRA regulations (part of
PBMS).
EPA also believes that method selection should be a project-
specific decision and therefore cannot recommend or approve any
methods--even SW-846 methods--as always being appropriate for any given
application. For that very reason, with this rule, EPA removed the
requirement to use SW-846 methods, except when the methods are the only
ones capable of measuring a particular property. Relying on the fact
that a method is contained in SW-846 does not guarantee that the method
will always generate effective data under any situation. If the SW-846
method is not an appropriate method for its intended application,
following it exactly could generate erroneous data and could fail to
demonstrate compliance with the RCRA requirements.
Second, EPA does not agree with the recommendation that it
categorically state that any method is always an effective means of
demonstrating compliance (with the exception of methods for the
analysis of method-defined parameters) since the Agency has no way of
knowing that a particular method is going to yield valid data in all
potential situations and it goes counter to the performance approach
which requires that regulated entities demonstrate compliance using
data of known and documented quality. The Agency believes that it is up
to the individual regulated entity to decide which methods are
appropriate to use for any given compliance demonstration and that this
determination should be initiated during the project planning stage.
When considering method selection, the analytical performance
indicators are key to the specific project goals that should be
considered. Examples of analytical performance indicators that might be
addressed include method sensitivity and selectivity, precision, bias,
and reproducibility. The data user may even choose to revise method
selection if additional information gathered during the project
indicate that the initial selection was not appropriate. Therefore,
method selection is a project-specific activity implemented by the
regulated entity, and EPA's only concern is that the generated data be
effective for its purpose, regardless of the method selection. The
Agency does recommend that a regulated entity seek assistance from its
regulating authority should the regulated entity have concerns
regarding the use of any particular method. EPA also notes that
guidance regarding demonstrating the performance of a given analytical
method can be found in EPA-published guidance documents (some of which
are listed above) and documents published by other Agencies (e.g.,
ASTM).
One commenter was concerned regarding how method performance would
be demonstrated under PBMS. The commenter claimed that implementation
of a PBMS approach is very difficult and that, for it to work, there
must be a ``reference method'' to be used as a benchmark against which
to measure other methods.
EPA notes that the RCRA program does not use reference methods.
Many different methods produce effective data for a particular project,
which are not necessarily ``equivalent,'' but all could be
``applicable.'' For example, there are many analytical methodologies
that can be used in analyzing a particular metal species (e.g., ICAP,
AA). In selecting a particular method for metal analysis, the analyst
will consider analytical costs, accuracy and sensitivity needed,
freedom from potential interferences, amount of sample required for an
analysis, reagents to be used, and other factors in the overall process
to select a method that will yield effective data at the lowest cost to
the user. These factors should be considered when evaluating any
method, including those published in SW-846, and the user needs to
conduct the appropriate verifications to demonstrate the
appropriateness of any method that is selected against its intended
application. There are a number of approaches that can be used to
demonstrate that a method is valid for a particular use. These include:
use of appropriate reference standards, analysis of spiked samples,
comparison of results to results generated using a method that employs
a fundamentally different measurement process and would not be subject
to the same potential interferences, etc. For further guidance in
demonstrating method validity, see the previously cited ASTM document D
6956-03, ``Standard Guide for Demonstrating and Assessing Whether a
Chemical Analytical Measurement System Provides Analytical Results
Consistent with their Intended Use.''
B. Public Comments Regarding Other Approaches
As explained in section III.B of the proposed rule preamble, EPA
considered several approaches to promoting ``method use'' flexibility
in the RCRA regulations. We selected the ``appropriate method''
approach because it is universally applicable to the subject RCRA
regulations. It also requires only minimal revisions to the regulations
for implementation.
In addition, the option to use ``appropriate methods'' is not new
to the RCRA regulations. For example, use of the TCLP, SW-846 Method
1311, is required for determining whether a waste is hazardous for the
toxicity characteristic (the TC). It generates an extract (the
leachate) which is subject to a determinative analysis for comparison
with the TC regulatory limits. However, the TCLP procedure does not
require specific analytical methods for the leachate determinative
analysis, nor does it specify the use of even SW-846 methods in general
for such analysis of the leachate. It allows method flexibility similar
to that proposed by this rule by stating in section 7.2.14: ``The TCLP
extract shall be prepared and analyzed according to appropriate
analytical methods.''
Nevertheless, in the proposed rule preamble, the Agency requested
the public's opinion on two alternative approaches that we considered
during development of this rulemaking.
1. As a variation to the ``appropriate method'' approach described
above, should we remove mention of SW-846 methods as examples of
potentially appropriate methods from the subject regulations?
2. In lieu of the ``appropriate method'' approach, should we
instead add specific measures of required measurement system
performance or data quality objectives to each regulation, such as done
in the comparable fuel rulemaking, and not mention or require the use
of an appropriate method (including any SW-846 methods)? In the
proposed MIR, we did not select this approach because it
[[Page 34544]]
might require significant regulatory changes with difficult to quantify
impacts.
Most of the commenters preferred that EPA retain mention of SW-846
in the regulations as examples of potentially appropriate methods.
However, some of these commenters appeared to believe that, by
mentioning SW-846 methods as examples, it meant that such methods will
always be appropriate for every data collection effort addressed by the
regulation, and thus the performance of other candidate methods should
be compared with the performance of the similar SW-846 method. One
commenter wanted the Agency to legally recognize that the SW-846
methods are appropriate methods under the RCRA regulations.
The Agency strongly disagrees with commenters that SW-846 methods
should be identified as always appropriate. As explained in section
III.A of this rule, the determination of an appropriate method should
be made on a project-specific basis and involves consideration of
various project-specific objectives and criteria. As noted, an
appropriate method might be one published by EPA in a different manual
from SW-846 or might be a method published by a different government
agency, a voluntary standards setting organization, or other well-known
scientific sources. Whether a method is contained in SW-846 is not a
primary criterion for determining if a method is appropriate. For
example, there is a common misconception that the different SW-846
methods for sample extraction all have the same extraction efficiency,
which is not the case at all, since the methods were intended to be
appropriate for different applications. Methods found in other
publications may be more appropriate based on the project-specific
considerations.
Regarding the addition of performance criteria to the regulations,
a few commenters did prefer that such criteria be added to the
regulations. However, these commenters did not provide suggestions
regarding how to best resolve those instances when such an approach
might result in requiring use of methods which are more accurate or
sensitive than necessary (with the result that monitoring costs may
increase unnecessarily) or in other cases would not yield data of a
sufficient quality to definitively determine if a facility is in
compliance with a regulatory or permit level. Given these impact issues
and the project-specific nature of what determines an appropriate
method, it would be contrary to the purpose of this rulemaking and very
difficult to develop and implement performance criteria and definitions
that would be universally applicable. EPA therefore decided against
adding criteria at this time to all of the regulations. We strongly
believe that the appropriate method determination should be made on a
project-specific basis by those familiar with the purpose of the
analysis and should not be dictated by regulatory definition. EPA
believes that generic performance criteria assigned by EPA would not
assure consistent application of PBMS, but rather might discourage a
PBMS application and flexibility in method selection and use. However,
to further evaluate this issue, the Agency's Forum on Environmental
Measurements (FEM) has formed an Action Team to address issues related
to implementation of the performance approach. It is anticipated that
the Action Team will address issues related to data quality and data
quality documentation for use by all Agency programs.
In conclusion, as a result of consideration of all comments, we
decided to not add performance criteria to the regulations. In
addition, unlike the proposal, we decided to not include any references
to SW-846 or ``using appropriate methods such as those found in * * *
SW-846'' in the regulatory provisions because those references to SW-
846 were unnecessary and, based on public comment, the regulated
community may continue to believe that SW-846 methods will always be
most appropriate.
C. Public Comments Regarding Impacts From Removal of Required Uses of
SW-846 Methods
In the preamble to the proposed rule, we summarized the expected
impacts on the regulated entities and the states, and requested public
comment on the assumptions made in the analysis. We also requested
public comment on the impact of this rule and how we might promote its
successful implementation. The paragraphs to follow summarize our
impact assumptions and provide our responses to some of the public
comments regarding these topics.
As a result of this final rule, you can use any appropriate
analytical test method in demonstrating compliance with the RCRA
regulations, except for those regulatory provisions involving method-
defined parameters. We believe that this action will not significantly
or adversely impact the regulated community or other potentially
affected parties because the Agency is not adding any additional
regulatory requirements to the RCRA regulations, but rather is
clarifying and expanding the flexibility that regulated entities have
had in selecting appropriate methods to employ to demonstrate
compliance whether or not such methods were described in SW-846. By
making it clear that one may use any appropriate method, regulated
entities may be able to cut the cost of compliance monitoring by using
less expensive methods. Regulated entities may continue to use SW-846
methods to demonstrate compliance when it is appropriate to do so, and
thus experience no impact from this rulemaking. EPA will also continue
to publish and update SW-846 methods and ensure their scientific
soundness by following peer review guidelines and requesting public
comment on the methods through Federal Register notices.
Thus, as we noted in section III.C of the proposed rule preamble,
the primary impact of this rule will be better analytical results
(e.g., due to paying better attention to method performance). The
Agency also anticipates a tendency toward lower costs during compliance
with the affected RCRA regulations because project planners may
identify methods that are potentially less costly to use. Meanwhile,
EPA also will continue to provide training and utilize our pool of
Agency technical experts to serve the public by answering questions
regarding the use of test methods during RCRA-related compliance
activities.
Also, a demonstration that another method is appropriate is already
allowed within RCRA-related sampling and analysis and will not involve
much more than what regulated entities already should be doing. For
example, as the regulated entity, you should already be setting method
performance goals in your Quality Assurance Project Plan (QAPP),
Sampling and Analysis Plan (SAP), or other systematic planning document
and then evaluating compliance with those goals based on data quality
indicators, including when using SW-846 methods.
Regarding public concerns about the comparability of data generated
by different methods for the same purpose, we noted in the proposed
rule preamble that this practice is not new because some regulations
already allow the use of more than one method. We also do not believe
that this should be a concern, provided that any alternative method is
also an appropriate method as defined above. Specifically, if both
methods generate effective data and meet the data quality objectives of
the project, then results from both methods will be acceptable for
demonstrating compliance. In addition, for situations where trends or
comparability are to be
[[Page 34545]]
determined, measurement quality objectives should be selected for use
in selecting methods to be used that will ensure that, for whatever
desired level of difference one desires to determine, the data will be
suitable for the purpose. This has always been EPA's approach in
comparing data by different methods, and it is not affected or changed
by this rule.
Some commenters preferred a more prescriptive approach in the
regulations because method-specific requirements remove the burden of
method-selection as it is believed that this translates into lower
costs and greater agreement between permit writers and other project
participants who may not have method-selection expertise. Because of
consequences of this approach, the Agency believes it is undesirable. A
major problem with the prescriptive-or mandated-methods approach is
that it can lead to data of poor quality which can result in an
incorrect assessment of compliance. Another problem is that the
regulated community may not systematically plan their data collection
efforts and thus not fully understand their project-specific goals.
Method-selection decisions should be project specific and thus,
specific methods should not be required in the regulations.
Some commenters also expressed concern regarding the impact of this
rule on existing RCRA permits. RCRA permits are typically effective up
to ten years. This rule will only effect new or reissued permits, and
only to allow more flexibility in method selection. Therefore, RCRA
permits will not be adversely impacted by this action.
Finally, this rule does not add new information collection or
reporting requirements for regulated entities. Section 260.22(i)
(reporting requirements for petitions to exclude wastes) and Sec. Sec.
264.13(b) and 265.13(b) (reporting requirements for owners and
operators of hazardous waste management facilities) provide sufficient
reporting requirements to cover RCRA-related testing and analysis
documentation regarding the use of other appropriate methods.
One commenter agreed, regarding impact of the rule, that the MIR
will greatly benefit those situations where repeated analyses are
needed, such as for a RCRA corrective action or for a WAP for a
hazardous waste treatment, storage, or disposal facility (TSDF).
However, the commenter also believed that smaller entities involved in
waste analyses, such as small quantity generators (SQGs) will probably
not benefit from the MIR. For the reasons given above, EPA believes
that the impact of this rule will not be significant for any generator,
including small quantity generators (SQGs), largely because the
flexibility of method selection will provide better analytical results
at a lower cost. Project planners and laboratories used by SQGs will
identify methods that are potentially less costly and yet provide
effective data. EPA believes that the regulated community will choose
appropriate methods based on cost and data quality advantages, and
therefore all regulated entities, including SQGs, could benefit from
this rule.
One other commenter believed that if PBMS is adopted, prior
approval by the State or other regulator of the method should be
mandatory. The commenter argued that State reviewers are more familiar
with SW-846 methods and data indicators and that a state's
unfamiliarity with other methods might mean the State may not perform a
timely review of the data.
As explained in the previous section, EPA believes that method
approval prior to use would be contrary to the intent and philosophy of
the performance concept and would negate the positive impacts of this
rule. However, as also noted, the regulated community can consult with
their regulating authority during the identification of performance
goals and the selection of appropriate methods. EPA appreciates the
commenter's concern regarding potentially negative impacts on the
timely review of data. It is true some delay in data review may occur
if the reviewer is not familiar with the procedure. Nevertheless,
review of data should not be a new step in the process since effected
entities should already be reviewing data indicators from the SW-846
methods during RCRA-related sampling and analysis. Once the reviewer
and user become more familiar with a new method, less time will be
needed to perform an equally thorough review. In the end, we believe
the benefits of modifying the rules will far outweigh these potential
impacts on data review time through the improvement of data
effectiveness and a decrease in other costs. To help mitigate any
potential negative impacts, we will continue to provide training and
our staff are available to assist you during all stages of the process.
Some commenters expressed a concern that this action will impose an
additional resource burden on States. In response, we note that the
regulatory changes in this rule are equivalent to or less stringent
than the existing Federal regulations which they amend. Therefore,
authorized States are not required to adopt and seek authorization for
this rulemaking within their programs. If a State believes that
adoption may be too burdensome on their resources, then they need not
adopt the revised regulations. Nevertheless, we encourage the adoption
of these or similar revisions by authorized States in order to promote
the national adoption of the performance approach in environmental
regulations, permits, and monitoring. In addition, if States choose to
adopt these revisions, the impact should not be significant since they
already conduct method selection and data quality reviews to determine
compliance with their testing and monitoring regulations.
Some commenters expressed a need for communication and training to
assist in implementation of the MIR. We agree and the Agency plans to
continue to provide education and training to States, EPA Regions, and
the regulated community regarding the implementation of this rule,
through such mechanisms as workshops, fact sheets, and Internet
training modules. Over the past seven years, OSW has offered program-
specific training (e.g., ``Analytical Strategy for the RCRA Program: A
Performance-Based Approach'') for EPA Headquarters, Regional, and State
personnel involved in RCRA activities that include sampling and
analysis. The Agency plans to expand its performance approach training
program and offer other courses on the evaluation of data and permit
writing from a PBMS and effective data standpoint. These communication
and training efforts will help ensure consistency in implementation of
this and other Agency performance-based rules by the States, Regions,
and regulated community and help limit any associated costs.
IV. Regulatory Revisions Involving Removal of SW-846 Requirements
In section IV of the proposed rule preamble, EPA listed and
discussed each of the proposed regulatory revisions which removed the
requirement to use SW-846 methods and stated that appropriate methods
may be used. We requested public comment on these individual regulatory
section revisions (e.g., comments regarding any impacts on
implementation of each affected regulation that we may have overlooked)
and in general did not receive any significant negative comments
regarding the removal of the SW-846 requirements from any of the
regulations. We are therefore finalizing the removal of the requirement
to use SW-846 in those regulatory sections.
[[Page 34546]]
In addition, we are finalizing revisions to three conditional
delistings in part 261, appendix IX, which were not included in the
proposed rule, but which, like those delistings that were included in
the proposal, unnecessarily require the use of SW-846 methods. We
announced our intent to revise these delistings in a memorandum to the
facilities and to the relevant EPA Regional offices. We gave the
entities three weeks to comment on the revisions. One of the affected
companies did not respond to the memorandum, while the other two
companies responded, but did not have comments regarding the revisions.
Therefore, we decided to proceed with finalizing the revisions to
these three delistings. The revisions to the conditional delistings are
very similar to the other conditional delistings. We did not receive
negative comments regarding the general removal of required uses of SW-
846 in any of the conditional delistings listed in the proposed rule.
We believe that these revisions are fully consistent with EPA's
original intent to make such changes to any conditional delisting, or
other regulations, which unnecessarily required the use of SW-846
methods for analyses other than for required MDPs.
The additional conditional delistings revised by this final rule
are found in Table 1 of appendix IX of part 261 and address delisted
wastes at the following facilities:
--Bekaert Corp., Dyersburg, TN
--OxyVinyls, L.P., Deer Park, TX
--Tokusen USA, Inc., Conway, AR
In addition, since publication of the proposed MIR, the Office of
Federal Register (OFR) revised its format for incorporation by
reference. Specifically, the OFR requires that the MDP methods
incorporated by reference at Sec. 260.11 be specifically mentioned in
the relevant sections of the regulations, and not just include
referrals to Sec. 260.11. Therefore, in the conditional exclusion
listings of part 261, appendix IX, we included a listing of the method-
defined parameter methods to replace our proposed language stating that
the methods listed in Sec. 260.11 must be used without substitution
when required. Those methods must be used as applicable to the
particular delisting.
Finally regarding the conditional delistings, we are taking this
opportunity to make several editorial corrections to Tables 1, 2 and 3
of appendix IX of part 261, which in no way substantially change or
remove any requirements. We are removing repeats of the Bekaert Corp.,
Dyersburg, TN, conditional delisting from Tables 2 and 3 of appendix IX
of part 261 because those entries were added to the tables in error.
The Bekaert Corp. conditional delisting is for an F006 waste, which is
from a non-specific source, and therefore the delisting only belongs in
Table 1, which lists wastes excluded from non-specific sources (i.e.,
``F'' coded listed wastes). Tables 2 and 3 of appendix IX of part 261
are meant to only list the conditional delistings of wastes excluded
from specific sources (Table 2, i.e., ``K'' coded listed wastes) or
from commercial chemical products, off-specification species, container
residues, and soil residues thereof (Table 3, i.e., ``P'' and ``U''
coded listed wastes). Similarly, we are removing the OxyVinyls, Dear
Park, TX, delisting from Table 1 and adding it to Table 2 of appendix
IX. This is necessary because the OxyVinyls' delisting addresses K017,
K019, and K020 wastes and was incorrectly placed in Table 1. Since
these are changes that do not affect the implementation of the
regulations, or add new or remove existing regulatory requirements, the
Agency is providing notice of the changes without opportunity for
comment.
Table 2 lists the regulatory revisions finalized by this rule to
remove the requirement to use SW-846 methods and allow the flexibility
to use other appropriate methods. As noted in the previous section of
this preamble, the proposed references to ``using appropriate methods
such as those found in * * * SW-846'' is not being included in the
final regulation because the Agency decided that those reference