EPA-450/3-89-023a
   Hazardous Waste TSDF -
Background Information for
Proposed RCRA Air Emission
          Standards

   Volume I - Chapters 1 - 8,
      & Appendices A - C
            Emission Standards Division
        U.S. ENVIRONMENTAL PROTECTION AGENCY
            Office of Air and Radiation
         Office of Air Quality Planning and Standards
         Research Triangle Park, North Carolina 27711

               June 1991

-------
                           DISCLAIMER
This report has been reviewed by the Emission Standards Division
of the Office of Air Quality Planning and Standards, EPA, and
approved for publication.  Mention of trade names or commercial
products is not intended to constitute endorsement or
recommendation for use.   Copies of this report are available
through the Library Services Office (MD-35), U.S. Environmental
Protection Agency, Research Triangle Park NC 27711, or from
National Technical Information Services, 5285 Port Royal Road,
Springfield VA 22161.
                                11

-------
                 ENVIRONMENTAL PROTECTION AGENCY

 Background Information and Draft Environmental Impact Statement
                               for
  Hazardous Waste Treatment, Storage, and Disposal Facilities -
           Tanks, Surface Impoundments, and Containers

                          Prepared  by:
Bruce C. Jordan
Acting Director, Emission Standards Division
U.S. Environmental Protection Agency  (MD-13)
Research Triangle Park, North Carolina  27711
(Date)
1.   Section 3004(n) of the Resource Conservation and Recovery
     Act as amended, requires EPA to develop standards for air
     emissions from hazardous waste treatment, storage, and
     disposal facilities  (TSDF) as necessary to protect human
     health and the environment.  The proposed standards would
     require organic emission control equipment be installed,
     operated, and maintained on all TSDF tanks, surface
     impoundments, and containers into which is placed hazardous
     waste with a volatile organic concentration equal to or
     greater than 500 parts per million by weight.

2.   Copies of this document have been sent to the following:
     Federal Departments of Labor, Health and Human Services,
     Defense, Transportation, Agriculture, Commerce, Interior,
     and Energy; the National Science Foundation; the Council on
     Environmental Quality; State and Territorial Air Pollution
     Program Administrators; EPA Regional Administrators; Local
     Air Pollution Control Officials; Office of Management and
     Budget; and other interested parties.

3.   The comment period for review of this document is 60 days
     from the date of publication of the proposed standards in
     the Federal Register.  Ms. Gail Lacy may be contacted ,at
     (919)  541-5261 regarding the date of the comment period.

4.   For additional technical information contact:

     Mr. Stephen A. Shedd
     Chemicals and Petroleum Branch, ESD  (MD-13)
  -•U.S. Environmental Protection Agency
   •- -Research Triangle Park, NC  27711
     Telephone:   (919)  541-5397

5.   Copies of this document may be obtained from:

     U.S. Environmental Protection Agency, Library  (MD-35)
     Research Triangle Park,  North Carolina  27711
     Telephone:   (919)  541-2777

     National Technical Information Service
     5285 Port Royal Road
     Springfield, Virginia  22161

-------
IV

-------
                                 CONTENTS
Chapter

          Figures	     ix
          Tables	     xi
          Abbreviations and Conversion Factors	     xv

  1.0     Introduction	    , i-i
          1.1  Control Options	    1-1
          1.2  Health and Environmental Impacts	    1-2
          1.3  Cost and Economic Impacts	    1-3

  2.0  .   Regulatory Authority and Standards Development	    2-1
          2.1  Regulatory Authority	    2-1
          2.2  Standards Development for Waste
               Management Air Emissions	    2-2

  3.0     Industry Description and Air Emissions	    3-1
          3.1  The Hazardous Waste Industry	    3-1
               3.1.1  General Hazardous Waste Description	    3-1
               3.1.2  Generators	    3-4
               3.1.3  Transporters	    3-5
               3.1.4  Treatment, Storage,  and Disposal Facilities...    3-7
               3.1.5  TSDF Emission Sources	   3-14
          3.2  Estimates of Organic Emissions	   3-18
               3.2.1  Emission Estimation  Data Requirements	   3-19
               3.2.2  Nationwide TSDF Emissions		   3-24
          3.3  References	   3-29

  4.0     Control  Technologies 	    4-1
          4.1  Application of Control Technologies to
               TSDF Emission Sources	•	    4-1
               4.1.1  Control Technology Categories	    4-1
               4.1.2  Organic Air Emission Control Efficiency	    4-2
               4.1.3  Secondary Air and Cross-Media Impacts	    4-4
          4.2  Suppression Controls	    4-5
               4.2.1  Fixed-Roof Tanks	    4-5
               4.2.2  Tank Floating Roofs	    4-9
               4.2.3  Pressure Tanks	   4-11
               4.2.4  Floating Membrane Covers	   4-12
               4.2.5  Air-Supported Structures	   4-15

-------
                            CONTENTS (continued)
Chapter
               4.2.6  Flexible Membrane Covers	   4-19
               4.2.7  Rigid Membrane Covers	   4-20
               4.2.8  Rigid Structures	   4-20
          4.3  Add-On Controls 	   4-20
               4.3.1  Carbon Adsorbers	   4-22
               4.3.2  Thermal Vapor Incinerators	   4-28
               4.3.3  Catalytic Vapor Incinerators	   4-30
               4.3.4  Flares	   4-33
               4.3.5  Boilers and Process Heaters	   4-36
               4.3.6  Condensers	   4-36
               4.3.7  Absorbers	   4-39
          4.4  Organic Removal and Hazardous Waste
               Incineration Processes	   4-39
               4.4.1  Steam Stripping	   4-39
               4.4.2  Air Stripping	   4-45
               4.4.3  Thin-Film Evaporation	   4-49
               4.4.4  Batch Distillation	   4-52
               4.4.5  Dewatering	   4-56
               4.4.6  Hazardous Waste Incineration	   4-59
          4.5  Process Modifications	   4-63
               4.5.1  Petroleum Refinery Waste Coking	   4-63
               4.5.2  Submerged Loading	   4-65
               4.5.3  Subsurface Injection	   4-66
               4.5.4  Waste Fixation Mechanical Mixing	   4-66
          4.6  Work Practice Modification	   4-68
             •  4.6.1  Housekeeping in Drum Storage Areas	   4-68
               4.6.2  Leak Detection and Repair	   4-69
          4.7  Summary of Control Technologies Selected
               for Control Option Analyses	   4-70
          4.8  References	   4-78

  5.0     Control Options	     5-1
          5.1  Control Option Concept	     5-1
          5.2  Emission Sources, Controls, and Action
               Levels Considered in Developing Control
               Options	     5-2
               5.2.1  Emission Sources	     5-2
               5.2.2  Controls	     5-2
               5.2.3  Action  Levels	     5-5
          5.3  Selection  of Control Options...,	     5-5
          5.4  Baseline for Nationwide Impacts Estimates	     5-8
               5.4.1  Land Disposal Restrictions	     5-9
               5.4.2  TSDF Air Standards for  Equipment
                      Leaks and Process Vent  Control	   5-10
               5.4.3  New Source Performance  Standards  (NSPS)
                      for Volatile Organic Storage Vessels	   5-11
          5.5  Reference	   5-13
                                     VI

-------
                             CONTENTS  (continued)

 Chapter                                                                 page

   6.0      National  Organic  Emissions  and  Health  Risk  Impacts	     6-1
           6.1   Organic  Emission  Impacts	„	     6-1
           6.2   Human  Health Risks	     6-7
                6.2.1  Annual  Cancer  Incidence	     6-7
                6.2.2  Maximum Lifetime Risk	     6-8
                6.2.3  Noncancer  Health Effects Assessment--
                      Acute and  Chronic Exposures	    6-11
           6.3   Other  Environmental Impacts	    6-13
           6.4   References	    6-17

   7.0      Costs of  the  Control Options	     7-1
           7.1   Control  Costs  Development	     7-1
                7.1.1  Methodology for Model Units	     7-2
                7.1.2  Derivation of Unit  Costs to Estimate
                      Nationwide Costs of Control. Options	     7-4
           7.2   Summary  of Nationwide Control Costs for Control
                Options	     7_5
           7.3   Cost Effectiveness of Control Options	     7-7
           7.4   References	    7_10

  8.0      Economic  Impacts	     8-1
          8.1   Industry Profile	',[',     8-2
               8.1.1  The Supply Side	     8-3
               8.1.2  The Demand Side	    8-10
               8.1.3  Market Outcomes	    8-14
          8.2  Analytical Approach	    8-14
               8.2.1  Model Overview	    8-15
               8.2.2  Model Design	    8-18
          8.3   Economic Impacts	    8-24
               8.3.1  Price and Quantity Adjustments	    8-25
               8.3.2  Regulatory Costs	    8-29
               8.3.3  Emissions and Cost  Effectiveness	   8-29
               8.3.4  Facility Closures	   8-41
               8.3.5  Employment Effects	   8-43
               8.3.6  Small Business Effects	„	   8-45
          8.4  References	   8-52

Appendix                                          .                     page

  A       Evolution of Proposed Standards	    A-l

  B       Index to Environmental  Impact Considerations	    B-l

  C       Emission Models and Emission Estimates	    C-l
          C.I   Emission  Models	    C-4
               C.I.I  Description of Models	    C-4
               C.I.2  Comparison  of Emission Estimates
                      with Test Results...	   C-14
                                    vn

-------
                            CONTENTS (continued)
Appendix
               C.I.3  Sensitivity Analysis	   C-16
          C.2  Model TSDF Waste Management Unit Analyses	   C-18
               C.2.1  Model Unit Descriptions	   C-19
               C.2.2  Model Wastes	   C-47
               C.2.3  Summary of Model Unit Analysis of
                      Emission Reductions and Control Costs	   C-50
          C.3  References	   C-85
(Bound separately in Volume II)
  D       Source Assessment Model	    D-l
  E       Estimating Health Effects	    E-l
  F       Test Data	    F-!
(Bound separately in Volume III)
  G       Emission Measurement and  Continuous Monitoring	    G-l
  H       Suppression and  Add-On Control  Device Cost Estimates
          and Suppression  Control Efficiency Estimates	    H-l
  I       Supporting Documents for  the Economic Impact  Analysis	    1-1
  J       Exposure  Assessment  for Maximum Risk and  Noncancer
          Health Effects	    J-l
  K       Secondary Air  and Cross-Media  Impact Estimates	    K-l
  L       90-Day Tanks and Container Impacts	    L-l
                                    vn i

-------
                                   FIGURES
Number
Page
  3-1     Simplified hazardous waste system from generation to
          disposal	     3-2
  3-2     Estimate of physical characteristics of RCRA
          hazardous wastes	"	     3-6
  3-3     Two examples of onsite hazardous waste land treatment
          operations	    3-10
  3-4     Two examples of active landfill  operations	    3-11
  3-5     Example onsite hazardous waste storage facility	    3-12
  3-6     Source Assessment Model  (SAM)  input files used in
          estimating nationwide treatment, storage, and
          disposal facilities (TSDF) uncontrolled air emissions	    3-25

  4-1     Storage tank covers	     4-7
  4-2     Typical air-supported structure  	    4-16
  4-3     Carbon canister unit 	    4-24
  4-4     Schematic diagram of thermal  incinerator system	    4-29
  4-5     Schematic diagram of catalytic incinerator system 	    4-32
  4-6     Steam-assisted elevated  flare  system 	    4-34
  4-7     Schematic diagram of a shell-and-tube surface
          condenser 	    4-38
  4-8     Schematic diagram of a steam stripping system	    4-41
  4-9     Schematic diagram of an  air stripping system	    4-46
  4-10    Schematic diagram of a thin-film evaporator system 	    4-50
  4-11    Schematic diagram of batch distillation with
          fractionating column 	    4-54
  4-12    Dewatering system with enclosed  dewatering device 	    4-58
  4-13    Hazardous waste incinerators  	    4-62

  8-1     A market supply curve constructed by summing
          four firms'  supply curves	'	    8-17
  8-2     Hypothetical price and output  adjustments due to
          a market supply shift induced  by air emission
          regulations	    8-19
                                    IX

-------

-------
                                   TABLES
Number                                                                 Page

  1-1     Residual Health and Environmental Effects of
          Control Options for TSDF Organic Air Emissions	    1-4

  3-1     Resource Conservation and Recovery Act (RCRA)
          Hazardous Waste Management Definitions	    3-8
  3-2     Nationwide Quantity of Hazardous Waste Managed
          by Specific Processes	    3-9
  3-3     Hazardous Waste Management Process Emission Sources	   3-15
  3-4     Summary of Selected Model Hazardous Waste Management
          Unit Uncontrolled Organic Emission Estimates for
          Model Wastes	„	   3-22
  3-5     Nationwide Uncontrolled TSDF Organic Emission
          Estimates		   3-30

  4-1     TSDF Control Technology Categories	    4-3
  4-2     Emission Control Options Used for Selecting
          TSDF Control Options	   4-71
  4-3     Emission Control Efficiencies Used in
          Estimating Nationwide Impacts of Control  Options	   4-73
  4-4     Generic Control Device Definitions	   4-77

  5-1     TSDF Emission Source Categories 	    5-3
  5-2     TSDF Air Emission Control Options	    5-6
  5-3     Control Requirements Under the Clean Air Act
          for Volatile Organic Liquid Storage Vessels	   5-12

  6-1     Summary of Nationwide Organic Air Emissions and
          Health Risk Impacts for Uncontrolled, Baseline,
          and Five Control Options	    6-2
  6-2     Nationwide TSDF Emissions for the Uncontrolled,
          Baseline, and After Control Options	    6-4
  6-3     Nationwide Cancer Incidence from TSDF Emissions by
          Source Category	    6-9
  6-4     Maximum Lifetime Risks from TSDF Emissions	   6-12
  6-5     TSDF Control Device Operating Conditions  Selected for
          Secondary Air and Cross-Media Impact Estimates	   6-14
  6-6     Summary of Nationwide Annual Secondary Air and
          Cross-Media Impact Estimates for Control  Options
          1 Through 5	   6-16

-------
                             TABLES (continued)
Number
Page
  7-1     Estimated Total Capital Investment and Total
          Annual Cost Per Unit of Waste Throughput by
          Source Category for Five Control Options 	    7-6
  7-2     Estimated Nationwide Total Capital Investment and
          Total Annual Cost for Five Control Options	,.    7-8
  7-3     Nationwide TSDF Cost Effectiveness of Five
          Control Options	    7-9

  8-1     Comparison of Unit Costs per Metric Ton	    8-5
  8-2     Parameters of the Unit Cost Function	    8-6
  8-3     Volume of Waste Managed by Sector, 1986	    8-8
  8-4     Supply Elasticities for Hazardous Waste
          Management Services by Sector	    8-9
  8-5     Consumption of Hazardous Waste Management
          Services and Value of Shipments by Sector, 1986	   8-12
  8-6     Cost Shares and Demand Elasticities by Sector	   8-13
  8-7     Market Share Parameters for Hazardous Waste
          Management Services, by Sector	   8-22
  8-8     Control Option Shift Parameters by Sector, Percent	   8-23
  8-9     Number of Treatment, Storage, and Disposal
          Facilities (TSDF) Affected by the Control Options	   8-26
  8-10    Price Adjustments by Control Option for Goods
          and Services Produced by Hazardous Waste
          Generators, Percent	   8-27
  8-11    Quantity Adjustments by Control Option for
          Goods and Services Produced by Hazardous
          Waste Generators, Percent	   8-28
  8-12    Quantity Adjustments in Waste Generation and
          Management by Generating Sector:  Control Option 1	   8-30
  8-13    Quantity Adjustments in Waste Generation and
          Management by Generating Sector:  Control Option 2	   8-31
  8-14    Quantity Adjustments in Waste Generation and
          Management by Generating Sector:  Control Option 3	   8-32
  8-15    Quantity Adjustments in Waste Generation and
          Management by Generating Sector:  Control Option 4	   8-33
  8-16    Quantity Adjustments in Waste Generation and
          Management by Generating Sector:  Control1 Option 5	   8-34
  8-17    Price and Quantity Adjustments in the Market for
          Commercial Hazardous Waste Management Services	   8-35
  8-18    Compliance Costs by Control Option Without
          Quantity Adjustments, $106/yr	   8-36
  8-19    Compliance Costs by Control Option with
          Quantity Adjustments, $106/yr		   8-37
  8-20    Capital Costs by Control Option,  $106/yr	.	   8-38
  8-21    Compliance Costs as Percent of Hazardous
          Waste Management Costs, Percent	   8-39

-------
                             TABLES (continued)
Number                                                                 Page

  8-22    Emissions and Cost Effectiveness by Control Option	   8-40
  8-23    Potential Facility Closures by Control
          Option and Sector	   8-42
  8-24    Potential Employment Effects by Control
          Option and Sector,  Number of Jobs	   8-44
  8-25    Small Business Administration Size Criteria
          by SIC Code	   8-47
  8-26    Baseline Statistical Data for Small Commercial
          Facilities with Estimated Sales Revenue Less
          Than $5 Million (Annual Values)	   8-49
  8-27    Effects of the Most Stringent Regulation
          (Option 1) on Small Commercial Facilities with
          Estimated Sales Revenue Less Than $3.5 Million..	   8-51

  A-l     Evolution of Proposed Treatment, Storage, and
          Disposal Facility Air Standard	    A-6

  C-l     Design and Operating Parameters of Hazardous
          Waste Surface Impoundment and Uncovered
          Tank Model Units.	   C-20
  C-2     Design and Operating Parameters of Hazardous
          Waste Land Treatment Model Units	   C-32
  C-3     Design and Operating Parameters of Hazardous
          Waste Fixation Pit, Wastepile Storage,
          and Landfill  Disposal Model Units	   C-33
  C-4     Design and Operating Parameters of Hazardous
          Waste Transfer, Storage, and Handling Operation
          Model Units	   C-41
  C-5     Model Waste Compositions	   C-48
  C-6     Summary of TSDF Model Unit Analysis Results	   C-51

-------
XIV

-------
                   ABBREVIATIONS AND CONVERSION FACTORS
     The EPA policy is to express all measurements in Agency documents in
the International System of Units (SI).  Listed below are abbreviations
and conversion factors for equivalents of these units.
Abbreviations

L - liters


kg - kilograms


Mg - meg ag rams
m - meters
cm - centimeters

kPa - kilopascals
ha - hectares


rad - radians


kW - kilowatts
                Conversion Factor

                liter X 0.26   = gallons
                gallons X 3.79 = liters

                kilograms X 2.203 = pounds
                pounds X 0.454    = kilograms

                megagram XI       = metric tons
                megagram X 1.1     = short tons
                short tons X 0.907 = megagrams

                meters X 3.28       = feet
                centimeters X 0.396 = inches

                kilopascals X 0.01 = bars
                bars X 100 '        = kilopascals
                kilopascals X 0.0099 = atmospheres
                atmospheres X 101    = kilopascals
                kilopascals X 0.145 = pound per
                  square inch
                pound per square inch X 6.90 =
                  kilopascals

                hectares X 2.471 = acres
                acres X 0.40469  = hectares
                radians X 0.1592
                revolutions X 6.281

                kilowatts X 1.341
                horsepower X 0.7457
                    revolutions
                    radians

                    horsepower
                    kilowatts
           Frequently used measurements in this document are:
                 0.21
                 5.7
                30
                76
               800
                 1.83
            210
          5,700
         30,000
nP   ~   76,000 L
m3   ~  800,000 L
kg 02/kW/h
kW/28.3 m3
          55 gal
       1,500 gal
       8,000 gal
      20,000 gal
  ~  210,000 gal
 3 Ib 02/hp/h
1.341 hp/103 ft3
                       •"•/^^•'J?** ill         .1 • ^ ^ J. flhS/^W  I W

                       kPa«m3/g«mol   «   0.0099 atm»m3/g«mol
                                    xv

-------

-------
                              1.0   INTRODUCTION

     Hazardous waste treatment, storage, and disposal facilities  (TSDF)
managing wastes containing organics are potential sources of organic air
emissions.  These organic air emissions can contain toxic chemical com-
pounds as well as ozone precursors.  Cancer and other adverse noncancer
human health effects can result from exposure to these organic air emis-
sions.  In addition, these emissions contribute to formation of ozone,
which causes adverse impacts on human health (e.g., lung damage)  and the
environment (e.g.\ reduction in crop yields).  Excessive ambient  ozone
concentrations are a major air quality problem in many large cities
throughout the United States.
     In 1984, Congress passed the Hazardous and Solid Waste Amendments
(HSWA) to the Resource Conservation and Recovery Act (RCRA) of 1976.
Section 3004(n) of HSWA directs the U.S. Environmental Protection Agency
(EPA) to promulgate regulations for the monitoring and control of air
emissions from hazardous waste TSDF as may be necessary to protect human
health and the environment.  Standards are being developed by EPA under the
authority of §3002 and §3004 of RCRA to reduce organic air emissions from
TSDF.  The standards would apply to owners and operators of permitted and
interim status TSDF under RCRA Subtitle C.  This document presents informa-
tion used in the development of the proposed RCRA air emission standards
for TSDF.
1.1  CONTROL OPTIONS
     To select a basis for the proposed standards, EPA identified and eval-
uated a variety of possible strategies for applying organic air emission
controls to TSDF.  Each strategy considered by EPA is referred to as a
"control option."  Different control options were identified by varying the
types of waste management units that would need to use emission controls
and the level  of organic air emission reduction that would be required for
                                     1-1

-------
the emission controls.  Each control option defines a unique set of wastes
(based on the volatile organic content of the waste)  and organic air emis-
sion control levels that allows EPA to perform an analysis to estimate the
nationwide human health and environmental impacts expected to occur if
standards based on a particular control option were promulgated.  The EPA
compares the control option impacts relative to a common set of reference
values called the "baseline."  The baseline represents the estimated human
health and environmental impacts that would occur in the absence of devel-
oping the standards.
     The EPA selected five control options for analysis.  All five of the
control options would require that all TSDF tanks, surface impoundments,
and containers managing hazardous waste with a volatile organics content
greater than a specified concentration use emission controls.  The speci-
fied volatile organic concentration at which a waste stream would be
required to use emission controls is referred to as the "action level."
The primary differences between the control options are the value used for
the action  level and whether a closed vent system and control device are
used in combination with the cover for the tank and surface impoundment
units requiring emission controls.  A detailed description of the five
control options is presented in Chapter  5.0 of this document.
1.2  HEALTH AND ENVIRONMENTAL. IMPACTS
     In evaluating the  health  and environmental  impacts of the  emission
control options, EPA  relied primarily on  the use of computerized analytical
models.  These models are  complex computer programs that  process a wide
variety of  information  and data concerning the TSDF industry  in the  United
States.  The data processed by the model  include results  from nationwide
surveys of  the TSDF industry,  characterizations  of TSDF processes  and
wastes, as  well as engineering simulations of the  relationships between:
 (1) waste management  unit  type, the quantity and composition  of the  waste
managed in  the unit,  and the  air  emission mechanism;  (2)  air  emission
control technology, control efficiencies,  and associated  capital and
operating costs; and  (3) population exposure to  TSDF  air  emissions  and
resulting nationwide  cancer  incidence.
     The Source Assessment Model  (SAM)  provides  estimates of  the nationwide
 impacts by  summing  the  estimated  facility impacts  across  all  facilities in
                                      1-2

-------
the model.  Further information on the emission models and emission
estimates is included in Appendix C; the SAM is further discussed in
Appendix D.  The estimated emissions were used as input to dispersion and
risk models that produce an estimate of risk and cancer incidence in the
exposed population.  These health effects were estimated based on a
composite unit risk factor, which is an emission-weighted average of the
unit risk factors for the individual organic carcinogens contained in the
emissions.  The Human Exposure Model was used to estimate cancer incidence,
and the Industrial Source Complex Long-Term Model was used to estimate the
maximum lifetime risk to the most exposed individual (MET).  The health
effects analysis included cancer risk to the MEI and noncancer impacts,
which may be long-term (chronic) or short-term (acute) health effects.  The
assessment methodology for chronic, noncancer effects involves a comparison
of estimated ambient concentrations with reference air concentrations, or
health "thresholds."  Additional information on the health effects analyses
is included in Appendixes E and J.  The estimated health and environmental
impacts of the selected control options are shown in Table 1-1.
1.3  COST AND ECONOMIC IMPACTS
     Estimates of the nationwide costs for the control options .are based on
estimates of the control costs for individual waste management units within
a TSDF.  For each control option, EPA developed a detailed estimate of the
total capital investment, annual operating costs, and total annual costs of
each emission control technology applied to each waste management unit.  To
obtain nationwide costs from model unit costs,  a weighted average model
unit control cost was derived for each control  applied to each waste
management unit.  These control costs, divided by the weighted average
model unit throughput, provided cost factors used to generate control cost
estimates for each TSDF.  The SAM was used to generate nationwide costs by
summing individual facility costs across all facilities.  Additional
information on the cost impacts for the control options is presented in
Chapter 7.0.
     The%economic analysis results indicate that all five control options
are projected to have small impacts—less than 1 percent—on the unit cost
of hazardous waste management services at facilities that treat and dispose
                                     1-3

-------
           TABLE 1-1.   RESIDUAL HEALTH AND ENVIRONMENTAL EFFECTS OF
               CONTROL OPTIONS FOR TSDF ORGANIC AIR EMISSIONS9
Control
option
number
BASELINE
1
2
3
4
5
Action
level ,
ppm
--
0
500 '
500
1,500
3,000
Organic
emissions,
103 Mg/yr
1,800
92
96
130
140
180
Cancer
incidence,
cases/yr
140
5.9
6.4
8.4
14
16
Maximum
individual
risk,
lifetime
2 X ID'2
5 x 10-4
5 x ID'4
5 x 10-4
P v m-4
o x ID ^
9 x ID'4
TSDF - Treatment, storage, and disposal facility.
  — = Not applicable.

aControl options 1 through 5 apply to wastes containing organics at con-
 centrations greater than the action level associated with the particular
 option.  They entail covers and control devices for tanks (including waste
 fixation) and impoundments, and covers and submerged loading of containers.
 For covered storage and quiescent treatment tanks, venting to a control
 device is required if the vapor pressure of the waste in the tank exceeds
 10.3 kPa (1.5 psi) for control options 1, 2, 4, and 5.  No control devices
 are applied to covered storage and quiescent treatment tanks in control
 option 3.  The impacts presented in this table are only for the TSDF units
 affected by the proposed standards.
                                     1-4

-------
these wastes.  The unit-cost increases for storage-only facilities are
substantial for several industrial sectors when viewed as a share of
hazardous waste management costs.  These cost increases translate into
nationwide compliance costs of between $4 million and $31 million for
storage-only facilities.  The economic analysis is further described in
Chapter 8.0.
                                    1-5

-------

-------
             2.0  REGULATORY AUTHORITY AND STANDARDS DEVELOPMENT

     This chapter presents an overview of EPA's regulatory framework for
controlling organic air emissions from hazardous waste treatment, storage,
and disposal facilities (TSDF).  Regulatory authority for the control of
air emissions from hazardous waste TSDF under the Resource Conservation and
Recovery Act (RCRA),  as amended, is discussed in Section 2.1.  The EPA's
standards development plan for controlling waste management air emissions
under RCRA and the Clean Air Act (CAA) is summarized in Section 2.
2.1  REGULATORY AUTHORITY
     In November 1984, Congress passed the Hazardous and Solid Waste
Amendments to the Resource Conservation and Recovery Act of 1976.  As
amended, RCRA §3004 authorizes EPA to establish standards that regulate the
operation of hazardous waste TSDF.  Air emission standards are required
under §3004(n), which states:
     ... the Administrator shall promulgate such regulations for the
     monitoring and control of air emissions at hazardous waste
     treatment, storage, and disposal facilities, including but not
     limited to open tanks, surface impoundments, and landfills, as
     may be necessary to protect human health and the environment.
     Section 3004(n)  does not confer new authority, but rather requires the
Agency to exercise its preexisting authority to control air emissions from
hazardous waste management.  Several rulemakings related to the control of
air emissions already have been undertaken by EPA under RCRA authority.
For example, EPA has promulgated standards for the control of air emissions
from hazardous waste incinerators (40 CFR 264, Subpart 0).  Standards for
air emissions from the burning of hazardous waste in boilers and industrial
furnaces and amendments to Subpart 0 standards were proposed April 27,  1990
(55 FR 17862).  The Agency also has promulgated standards under 40 CFR 264
and 265 for windblown dust from wastepiles, landfills, and land treatment
                                     2-1

-------
operations.  Additionally, final standards for miscellaneous units and for
research, development, and demonstration units under 40 CFR 264, Subparts X
and Y, contain provisions that require prevention of air releases that may
have adverse effects on human health or the environment.
     Air emissions from hazardous wastes are generated or released from
numerous sources at TSDF.  Air emission sources identified by EPA to date
include waste treatment processes such as distillation and fixation, equip-
ment leaks, surface impoundments, tanks, containers, landfills, wastepiles,
and land treatment facilities.  Organic air emissions from hazardous wastes
managed in these sources include photochemically reactive and nonphotochem-
ically reactive organics, some of which are toxic or carcinogenic, and also
may include toxic or carcinogenic inorganic compounds.  Depending on the
source, particulates (including metals, aerosols of organics, dust, as well
as toxics and carcinogens) also may be released.  Reduction of the toxic or
carcinogenic emissions will reduce the incidence and risk of both cancer
and noncancer health effects in the exposed population; reduction of ozone
precursors in the organic emissions also will assist in reducing ozone
formation.
2.2  STANDARDS DEVELOPMENT FOR WASTE MANAGEMENT AIR EMISSIONS
     Given the wide variety of TSDF sources and the complex analyses and
data required to assess emissions from these sources and their impacts, EPA
is taking several separate actions.  On June 21, 1990 (55 FR 25454), EPA
promulgated standards for the control of organic air emissions from
(1) hazardous waste management process vents associated with distillation,
separation, fractionation, air or steam stripping, and thin-film evapora-
tion processes under Subpart AA to 40 CFR Parts 264 and 265, and (2) leaks
in piping and other equipment managing hazardous waste under Subpart BB to
40 CFR Parts 264 and 265.
     The EPA also is further addressing the potential health effects
resulting from exposure to particulate emissions at TSDF.  This is being
done through development of detailed guidance to supplement existing
standards under 40 CFR 264 and 265 for windblown dust from landfills, land
treatment facilities, and wastepiles.
     The standards developed for proposal that are supported by this
background information document (BID) would control the class of organic
                                     2-2

-------
air emissions from surface impoundments, tanks (including vents on closed,
vented tanks), containers, and waste fixation process units.  The EPA is
also evaluating the need for standards to control emissions of individual
chemical constituents from these sources.  Standards for individual consti-
tuents will be developed separately in the future as necessary to address
residual health risk that may remain after controls are implemented for
organic emissions as a class.
     The control options and their associated environmental and health risk
impacts for organic air emissions from surface impoundments, tanks,
containers, and waste fixation process units are discussed in Chapters 5.0
and 6.0 of this document.  The evolution of the standards for these sources
is described in Appendix A of this document.  As discussed in Appendix A,
this BID reflects revisions that have been made based on comments received
since the May 18, 1988, meeting of the National Air Pollution Control
Techniques Advisory Committee.  In the next step of the standards develop-
ment process, a draft proposal package will be assembled and reviewed by
the EPA Assistant Administrators and the Administrator for concurrence
before the standards are proposed in the Federal Register.  Information
received and generated in studies in support of the proposed standard is
available to the public in Docket F-90-CESP-FFFFF on file in Washington,
D.C.
     As part of the Federal Register notice of proposal, the public is
invited to participate in the standard-setting process.  The EPA invites
written comments and will hold one or more public hearings to receive
comments on the proposed standards from interested parties.  All public
comments will be analyzed, and written responses will be prepared.  A
document will be prepared that summarizes the comments and provides the
Agency's responses.  If public comments indicate that changes to the
proposed standards are warranted, the standards will be revised accordingly
before publication in the Federal Register.
                                     2-3

-------

-------
                 3.0  INDUSTRY DESCRIPTION AND AIR EMISSIONS

      This chapter presents a brief overview of the hazardous waste industry
 and a summary description of the techniques used in estimating nationwide
 organic air emissions for hazardous waste treatment,  storage, and disposal
 facilities (TSDF)  in the United States.  The hazardous waste industry and
 TSDF emission sources are described in Section 3.1.  The estimation of TSDF
 nationwide emissions is presented in Section 3.2.   Emission estimation
 techniques include the development and use of (1)  TSDF emission models,
 which provide a mechanism for analyzing air emissions from TSDF management
 processes and applicable emission control  technologies,  and (2) a computer
 program developed  to process  the data and  information on the TSDF industry
 and to perform emission calculations based on the  available data.   Discus-
 sions of air  pollution  controls  and control  strategies at TSDF follow in
 Chapters 4.0  and 5.0,  respectively.
 3.1   THE HAZARDOUS  WASTE INDUSTRY
      The hazardous  waste.industry in the United  States i-s diverse  and  com-
 plex.   The universe of  hazardous  waste  generators  represents  a broad  spec-
 trum  of industry types  and sizes.   Wastes  generated vary  considerably  in
 both  composition and  form; and the  waste management processes  and  practices
 used  in  treating, storing, and disposing of  hazardous  wastes  are also
widely  varied.   Figure 3-1 presents  a simplified waste system  flow chart
 for the  hazardous waste  industry.   Key  elements of the industry are:  gene-
 ration,  transportation,  treatment, storage,  and disposal.  The major ele-
ments of the hazardous waste industry are discussed in the following sec-
tions.
3.1.1  General Hazardous Waste Description
     General  waste descriptions include hazardous wastes  in the following
forms:  contaminated wastewaters, spent solvents residuals, still bottoms,
                                    3-1

-------
i
Q



to
O CO
*"i s
E co 9-
g-J .2
o Q
O
i
L




a-of
§0.

j
i




II
|.|

i
L
                                                                                                                    (0
                                                                                                                    (0
                                                                                                                    o
                                                                                                                    Q.
                                                                                                                    (0
                                                                                                                    S
                                                                                                                      -='
                                                                                                        O   w
                                                                                                           '
                                                                                                       1  1
                                                                                                           c
                                                                                                       2  m

                                                                                                       •5  S
                                                                                                        §> S
                                                                                                       cc  O
                                                                                                                    d>

                                                                                                                    I
                                                                                                                    (0
                                                                                                                    o
                                                                                                                    •5
                                                                                                                    s
                                                                                                                    ra
                                                                                                                    £
                                                                                                                    •o
                                                                                                                    0>
                                                                                                                    S
                                                                                                                    CO
                                                                                                                    I
                                                                                                                    Of
                                                                                                                    u.
                                                       3-2

-------
  spent  catalysts,  electroplating wastes, metal-contaminated  sludges,
  degreasing  solvents,  leaded tank bottoms, American  Petroleum  Institute
  (API)  separator  sludges, off-specification chemicals, and a variety of
  other  waste types.   In  reviewing waste data, more than 4,000  chemical con-
  stituents have been  identified as being contained in the various waste
  types  examined.1
      Title  40 of  the  Code of Federal Regulations (CFR), Part  261.3 (40 CFR
  261.3), defines hazardous waste as four categories:
      •    Characteristic wastes—wastes that exhibit any hazardous
           characteristic identified in 40 CFR 261 Subpart C,  includ-
           ing:  ignitibility,  corrosivity, reactivity, or extraction
           procedure (EP) toxicity
           Listed waste—wastes listed in 40 CFR 261, Subpart D
           Mixture rule wastes—wastes that are (1)  a mixture of solid
           waste and a characteristic waste unless the mixture no
           longer exhibits any  hazardous characteristic,  or (2) a mix-
           ture of a solid waste and one or more listed hazardous
           wastes
      *     Derived from rule wastes—anv solid waste generated  from the
           treatment,  storage,  or disposal  of  a hazardous  waste,
           including any sludge,  spill  residue,  ash,  emission control
           dust,  or leachate (but  not including precipitation runoff).
      Hazardous  wastes  are designated by Resource  Conservation  and Recovery
 Act  (RCRA) alphanumeric codes.   Codes  D001 through  D017 are  referred  to  as
 "characteristic wastes."  D001  represents wastes  that  are  ignitible  in
 character; D002,  those that  are corrosive; and  D003, those that  are  reac-
 tive.   Extracts of wastes that contain  toxic  concentrations  of specific
 metals, pesticides, or herbicides are  assigned  one of the codes  D004
 through 0017.
      "Listed wastes" encompass four groups of alphanumeric codes  published
 in 40 CFR 261, Subpart D.  Hazardous wastes generated from nonspecific
 industry sources such  as degreasing operations  and electroplating are
 listed  as codes beginning with the letter "F,"  e.g., FOOl.  Hazardous
wastes  from  specific generating sources such as petroleum refining are
assigned codes beginning with the letter "K," e.g.,  K048.   Waste codes
beginning with "P" or  "U" represent waste commercial chemical products and
manufacturing chemical intermediates (whether usable or off-specification).
                                    3-3

-------
     40 CFR 261,  "Identification and Listing of Hazardous Wastes," not only
 lists hazardous wastes but also identifies specific wastes that are
 excluded from regulation as hazardous.  These excluded wastes can be
 stored, treated,  or disposed of without a RCRA permit.
 3.1.2  Generators
     The overwhelming majority of hazardous wastes are produced by large-
 quantity generators, those firms that generate more than 1,000 kg of
 hazardous waste per month.  It has been estimated that there are about
 71,000 large-quantity generators of hazardous waste in the United States.2
 These generators  account for 99 percent of the 275 million Mg/yr of hazard-
 ous waste produced and managed under RCRA in 1985.3  Hazardous waste gener-
 ators are most prevalent in the manufacturing industries (standard indus-
 trial classification [SIC] codes 20-39).  Manufacturing as a whole accounts
 for more than 90  percent of the total quantity of hazardous waste gener-
 ated.  Among specific industries, the chemical, petroleum, metals, electri-
 cal equipment, and transportation industries are the major generators of
 hazardous wastes.  Two industry groups that stand out as generators are the
 chemical and petroleum industries (SIC 28 and 29); these industries alone
 account for more  than 70 percent of total waste generation.  The chemical
 industry (SIC 28), with only 17 percent of the generators, generated
 68 percent of all the hazardous wastes produced in 1981.  Another prominent
 group in the manufacturing sector was metal-related industries (SIC 33-37);
 these industries generated about 22 percent of all hazardous wastes in
 1981.4
     The 1981 Survey of Hazardous Waste Generators and Treatment, Storage,
 and Disposal Facilities (Westat Survey)5 showed that only 15 percent of the
 generators were nonmanufacturing or unclassified under SIC.  The survey
 results also provide estimates of number of generators producing specific
 types of hazardous wastes.  Just over half the generators indicated that
 they generate spent solvents,  both halogenated and nonhalogenated (RCRA
waste codes F001-F005).  Generators of sludges from wastewater treatment
 systems associated with electroplating and coating operations and gener-
 ators of quenching and plating bath solutions and sludges accounted for
 16 percent of the generator population.  Only 10 percent of the generators
                                    3-4

-------
 generated  listed hazardous  wastes  from specific  industrial  sources  (e.g.,
 slop oil emulsion solids  from the  petroleum refining industry—K049).
 Forty-three percent of generators  produce ignitible wastes  (RCRA waste code
 D001),  a third generated  corrosive wastes (D002),  and more  than  a quarter
 generated  wastes that failed EPA's test for toxicity (0004-D017).  Just
 under 30 percent of the generators reported hazardous wastes  that were
 spilled, discarded,  or off-specification commercial chemical  products  or
 manufacturing  chemical  intermediates  ("P" and  "U"  prefix waste codes).
      The physical characteristics  of  the 275 million Mg  of  RCRA  hazardous
 waste managed  in 1985 vary  from dilute wastewater  to metal-bearing  sludges
 to soils contaminated with  polychlorinated biphenyl (PCB).  Over 90 percent
 (by weight)  of RCRA hazardous waste is in the  form of dilute  aqueous waste.
 The remaining'wastes are  organic and  inorganic sludges and  organic  and
 inorganic  solids.  Figure 3-2 categorizes hazardous waste by  physical  char-
 acteristics.
      Although  small-quantity generators (those that generate  more than
 100 kg  and less than 1,000  kg of hazardous waste per month) represent  a
 large proportion of the number of  hazardous waste  generators  nationally
 (more than 26,000)J they account  for only a very  small  fraction of the
 hazardous  wastes generated.   About 25 percent  of the country's hazardous
 waste generators are small-quantity generators, but these generators con-
 tribute less than one-half  of 1 percent of the total  hazardous waste gener-
"ated.8  The majority of the small-quantity generators are automotive repair
 firms,  construction  firms,  dry cleaners,  photographic processors, and
 laboratories.   The  wastes produced by small-quantity generators  span the
 full  spectrum  of RC£A hazardous wastes.   According to EPA's National Small
 Quantity Hazardous  Waste  Generator Survey,9 the majority of small-quantity
 generator  waste is  derived  from lead  acid batteries;  the remainder  includes
 such  hazardous  wastes as  acids,  solvents,  photographic wastes, and  dry
 cleaning residues.
 3.1.3  Transporters
      Once  a RCRA hazardous  waste is generated, it  must be managed (i.e.,
 stored, treated,  or  disposed of) in accordance with legal requirements.
 Although nearly all  hazardous waste is managed to  some degree at the site
                                    3-5

-------
Aqueous Liquids
(252 X 106 Mg)
                                                               Organic Sludges (2 X 106 Mg)
                                                                     Organic Liquids
                                                                     (4X 106  Mg)

                                                                      Inorganic Solids
                                                                      {2 X 106 Mg)
                                                                      Aqueous Sludges
                                                                      (15 X 106Mg)
           Figure 3-2. Estimate of physical characteristics of RCRA hazardous wastes.6
                                       3-6

-------
 where it is generated, the Westat Survey has shown that only about one in
 six generators manage their hazardous waste exclusively onsite.10  Of those
 generators that ship hazardous wastes to offsite management facilities for
 treatment, storage, and disposal, roughly a quarter still  manage part of
 their hazardous wastes onsite.  Although the survey estimated that 84 per-
 cent of the generators ship some or all  of their hazardous wastes offsite,
 the vast majority of the quantities of hazardous waste are nonetheless
 managed onsite.  Data supplied by generators indicate that about 96 percent
 of all  generated hazardous wastes are managed onsite, with only 4 percent
 being shipped offsite for treatment,  storage, or disposal.
      In response to the movement of hazardous waste,  a large industry has
 developed that transports hazardous wastes from generators to TSDF.   It  has
 been estimated that over 13,000 transporters are involved  in moving  hazard-
 ous wastes by land  or water from generators  to TSDF.11
 3.1.4  Treatment, Storage,  and Disposal  Facilities
      A  significant  segment  of  the hazardous  waste industry is involved in
 hazardous waste management  (i.e.,  treatment,  storage,  and  disposal  activi-
 ties).   Table 3-1 provides  the RCRA definition of treatment,  storage,  and
 disposal.   TSDF must  apply  for and  receive a permit to operate  under RCRA
 Subtitle C  regulations.   The RCRA Subtitle C permit program  regulates  13
 categories  of waste management  processes.  There are  four  process  categor-
 ies  each  within  storage  and treatment  practices  and five categories  within
 disposal  practices.   Table 3-2  presents  the  13 major  categories  by RCRA
 process  code.
      Some of  the 13 RCRA  process  categories  can  be further classified  by
 characteristics of  the waste management  processes.  For example, tank
 treatment may  be quiescent or agitated/aerated  (referring to  the presence
 or  lack of movement/mixing of the liquid contained in the tank).  Such
 process varieties and similarities are reflected  in the characterization of
 the industry when estimating nationwide  TSDF emissions.  Figures 3-3
 through 3-5 provide a more detailed look at examples of the various manage-
ment processes.  As  can be seen from the range of treatment and disposal
processes, the industry is complex and not easily characterized.  The
hazardous waste industry is also dynamic; that is, in response to
                                    3-7

-------
         TABLE 3-1.  RESOURCE CONSERVATION AND RECOVERY ACT (RCRA)
                  HAZARDOUS WASTE MANAGEMENT DEFINITIONS3
      Term
              Definition
Storage
Treatment
Disposal facility
"Storage" means the holding of hazardous waste
for a temporary period, at the end of which the
hazardous waste is treated, disposed of, or  -
stored elsewhere.

"Treatment" means any method,  technique, or
process, including neutralization, designed to
change the physical, chemical, or biological
character or composition of any hazardous waste
so as to neutralize such waste, or so as to
recover energy or material resources from the
waste, or so as to render such waste non-
hazardous, or less hazardous;  safer to
transport, store, or dispose of; or amenable
for recovery, amenable for storage, or reduced
in volume.

"Disposal facility" means a facility or part of
a facility at which hazardous waste is
intentionally placed into or on any land or
water, and at which waste will remain after
closure.
aDefinitions are presented as stated in RCRA regulations (40 CFR 260.10)
 as of July 1, 1986.12
                                    3-8

-------
        TABLE  3-2.   NATIONWIDE QUANTITY OF  HAZARDOUS WASTE MANAGED BY
                            SPECIFIC  PROCESSES
       Waste
    management
      process
 RCRA       Number of active
process      facilities with
 code           process9
                  Waste quantity
              managed,3 10^ Mg/yr
Storage
                                        133
    Container
    Tank
    Wastepile
    Impoundment
Treatment
    Tank
    Impoundment
    Incineration
    Otherb
Disposal
    Injection well
    Landfill
    Land treatment
    Ocean disposal
    Impoundment

    Totalc
  SOI
  S02
  SOS
  S04
  T01
  T02
  T03
  T04
  D79
  D80
  D81
  D82
  D83
 1,440
   911
    57
   223
   291
   127
   158
   319
    61
    90
    54
    NA
    47

>2,300
                                        154
                                         49
                                        275
RCRA = Resource Conservation and Recovery Act,
  NA = Not available.
aBased on the 1986 Screener Survey.!3  Excludes facilities that manage
 less than 0.01 Mg/yr in storage, treatment, and disposal processes.
 Quantities were not reported in this survey by specific management
 process.

b"0ther" refers to physical, chemical, thermal, or biological treatment
 processes not occurring in tanks, surface impoundments, or incinerators.
cFacilities do not add up to about 2,300 because some facilities have more
 than one process.  Waste quantities presented do not add to the total of
 275 million Mg of hazardous waste produced and managed in 1985 because
 some facilities may process a waste in more than one management process.
 For example, a waste may be stored prior to treatment or treated prior to
 disposal.
                                    3-9

-------
                 CO
                 09
                 •o

                 CO
                            at
                           T3
I
J3
^35
Jd
 3

*O
*•«


4rf
 CO
 09
£
•o
 i
                                                                                          T3
                                                                                          
-------
              O
             • CM
       -r—
       ,    (O
       " '   *•
   •o

   (B
« c S «
 1-of
 1st
                  o
                  S-

              i  1
             I  i

             1  "
             £
             u.


             £
•s -g

'S  5
CO I-
                                       * =



                                       II
                                       o> a.
                              !§
                              .s a
                              u. o
                         «


                         I
                        oa


                        03
                              11
                              is
                              co o
      2?
      eo S
      S-o •

      •II
              i
              a.
              o
                                                                      •a

                                                                      

                                o

                               .3
                               §>

                               iZ
u a

•o o
o u
                                                                   to

                                                                   CO
                                u
                                3-11

-------

                          §
                      V
                                                  £
                                                  o
                                                   u
I
O
                       S.
                       '5.
                       a.
ES
QOT
                       S.
                       Q.
                  I

                  I
                                                                     o
                                                                     •s
                                                                     CD
                                                                     3
                                                                     x:
                                                                     O
                   Q.


                   X
                  111

                  in
                  m
                   as
 £ =
 3-0
 >- to
 Q p

"TI
                     3-12

-------
changing demands and regulations, the facilities change the ways wastes are
treated, stored, and disposed of.
     The total estimated quantity of hazardous wastes managed at more than
2,300 TSDF in 1985 was 275 million Mg.  The waste quantities handled by
each of the three main waste management processes (i.e., treatment, stor-
age, and disposal) are presented in Table 3-2.  The waste quantities given
in Table 3-2 will not sum to the total national estimate because some
wastes pass through more than one process; for example, a waste may be
stored prior to treatment or treated prior to disposal.  Also provided in
Table 3-2 is a breakdown of the number of active TSDF by specific type of
treatment, storage, or disposal process.  In the storage category, con-
tainer storage is a management process utilized by more than half the TSDF;
tank storage occurs at slightly more than a third of the TSDF.  Of the
treatment processes, tank treatment is widely practiced, but no single
treatment process is used in a majority of facilities.  In the disposal
category, landfills are the dominant disposal units operated at TSDF.
     The information presented above is taken from a TSDF data base of
waste management practices compiled for use in examining the industry and
its environmental and health impacts.  Three data bases were used to gener-
ate this TSDF data base.  Two major sources were the Hazardous Waste Data
Management System (HWDMS)14 and the 1981 Westat Survey, both of which are
EPA Office of Solid Waste (OSW) data bases.  More recent information from
the OSW 1986 National Screening Survey of Hazardous Waste Treatment, Stor-
age, Disposal, and Recycling Facilities (1986 Screener) was also used to
make the TSDF data base as current as possible.15  Each of these three data
bases provided a different level of detail regarding particular aspects of
the TSDF industry.  For example, the HWDMS provided waste management proc-
ess codes, wastes codes, and facility SIC codes.  The 1986 Screener pro-
vided information on total annual waste quantities managed by the facility
and operating status (active or closed) for the entire industry.  The
Westat Survey, on the other hand, deals with only a subset of the industry
but provides a greater level of detail regarding individual facility
operations;  for example, the distribution of waste quantities handled by
each waste management process is available for each facility in the data
base.
                                   3-13

-------
3.1.5  TSDF Emission Sources
     The organic emission sources associated with each type of storage,
treatment, and disposal process are summarized in Table 3-3.  The emission
sources in this table are arranged into six categories based on their
common emission characteristics and/or their routine association with other
processes.  These are (1) impoundments and tanks, (2) land treatment,
(3) landfills and wastepiles, (4) transfer and handling operations,  (5)
injection wells, and (6) incinerators.
     For open (or uncovered) surface impoundments and tanks, the major
source of organic emissions is the uncovered liquid surface exposed  to the
air.  The conditions under which liquids are stored in uncovered impound-
ments and uncovered tanks ranges from quiescent to highly turbulent  since,
in some cases, aeration and/or agitation are applied to aid in treatment of
the waste.  Emissions tend to increase with an increase in surface turbu-
lence because of enhanced mass transfer between the liquid and air.   For
both uncovered and covered storage tanks, loading and breathing losses are
a major source of emissions.
     At land treatment facilities, wastes are either spread on or injected
into the soil, after which they are normally tilled into the soil.  Other
activities that are likely to occur at land treatment facilities include
transfer,  storage, handling, and dewatering of the wastes to be land-
treated.  Examples would include loading and unloading of wastes in  vacuum
trucks and dewatering of wastes using one of the various types of available
filtration devices.  Each of the land treatment process stages illustrated
in Figure 3-3 is a potential source of organic air emissions.  The major
emission source associated with land treatment is the land treatment area
itself.
     A landfill  is a facility, usually an excavated, lined pit or trench,
into which wastes are placed for disposal.  Some existing landfills  may not
be lined;  however, all  new facilities are lined to meet RCRA permit
requirements.  All wastes containing liquids and destined for disposal in a
landfill must be treated or "fixed" to form a nonliquid material.  The
landfilling of waste is a source of organic emissions from several emission
                                   3-14

-------
      TABLE 3-3.  HAZARDOUS WASTE MANAGEMENT PROCESS EMISSION SOURCES
     Management process
     Emission source
 Impoundments and Tanks

 (S04, T02, D83) (S02, T01)

   Quiescent impoundments
      (storage & treatment)

   Quiescent tanks
      (storage & treatment)

       Uncovered
       Covered

   Aerated/agitated impoundments
      (treatment)

   Aerated/agitated uncovered tanks
      (treatment)

   Impoundment lining
   Impoundment inlet
Quiescent liquid surface
Quiescent liquid surface
Working and breathing losses

Turbulent liquid surface
Turbulent liquid surface
Dredging (exposed waste
  surface)3

Splash loading13
Land Treatment (D81)

   Land application



   Dewatering devices
Landfills (D80)  and Wastepiles (S03)

   Active landfill
Application of waste to soil
Applied waste before tilling
Applied waste after tilling

Vacuum pump exhaust for vacuum
  filters3
Exposed waste surface in belt
  filter presses  .
Filter cake collection and
  disposal
Transport of waste to landfill
  (open trucks)
Unloading and spreading of .
  wastes
Landfilled waste
Leachate (within the confines
  of the liner system)
                                                               (continued)
                                   3-15

-------
                           TABLE 3-3 (continued)
     Management process
     Emission source
Landfills and Wastepiles (con.)

   Closed landfill
   Wastepiles



   Waste fixation

     Pit and mixer




     Drum



Transfer and Handling Operations (SOI, S02)

   Vacuum trucks



   Open dump trucks




   Equipment leaks0




   Containers
     Drums
     Tank trucks
     Railroad tank cars
     Marine tankers
     Barges
     Dumpsters
Landfill surface gas vents and
  manholes
Leachate (within the confines
  of the liner system)

Wastepile surface
Leachate (within the confines
  of the liner system)
Splash loading into fixation
  pits'3
Mixing of waste and fixative
Mechanical mixer vents

Drum inspection3
Drum decanting3
In-drum fixation3
Vacuum pump exhaust
Spills during truck loading
Truck cleaning3

Waste surface during loading
  and transport
Spills
Truck cleaning3

Losses from pumps, valves,
  sampling connections, open-
  end lines, and pressure-
  relief devices
Waste loading
Spillage in transit
Spillage during waste loading/
  unloading
Exposed waste surface
Cleaning losses3
                                                               (continued)
                                   3-16

-------
                           TABLE 3-3 (continued)
     Management process
       source category
     Emission source
Injection Wells (D79)d

Incinerators (T03)e
Exhaust gas stacks
aNo emission estimating method exists for this source.

&No emission estimating method exists for this source.  Unlike enclosed
 sources such as tanks, this is an open'source and vapor saturation does
 not occur.

Emissions from equipment leaks are associated with all management
 processes that involve the use of pumps, valves, sampling connections,
 open-ended lines, and pressure-relief devices.

dThis management process is being regulated under a different standard.
 The equipment leak emissions related to the injection well disposal
 process are evaluated in this document.

elncinerator emission sources, such as exhaust gas stacks, are regulated
 under 40 CFR 264, Subpart 0, "Incinerators."  The equipment leak emissions
 related to incineration are evaluated in this document.
                                   3-17

-------
points, as illustrated in Figure 3-3.  This figure shows typical process
stages for two variations in landfill processing; each of the processing
steps identified is a potential emission source.  The landfill surface,
whether open, covered with earth daily, or closed with a cap is an emission
source.  A waste fixation pit is another source of organic emissions that
could be associated with landfills.  Activities at the landfill, such as
waste transport and waste unloading and spreading, are also sources of
emissions.  Wastepiles are similar to landfills and the same emission
sources can be found; they are, in essence, temporary landfills.
     Each of the process steps illustrated in Figure 3-5 is a potential
emission source associated with hazardous waste transfer, storage, and
handling operations.  Loading operations contribute to overall emissions,
especially splash loading of waste as opposed to submerged loading.  Spills
also occur during waste transfer and handling and, for liquid wastes that
are pumped, emissions may occur from fugitive sources such as pumps and
valves or at open-ended lines, pressure-relief valves, and sampling connec-
tions.  Organic emissions are associated with all three of the storage
methods shown in Figure 3-5:  drums, dumpsters, and tanks.
     Miscellaneous sources of emissions such as drum cleaning or the crush-
ing and landfilling of empty drums containing waste residues also contrib-
ute to organic air emissions.  The improper handling of drum residue can
lead to emissions along with waste residues lost to the environment by
uncontained drum crushing operations.  In addition, RCRA permit conditions
require annual dredging of surface impoundments; the dredging operation, a
waste transfer process, may also be a source of organic emissions.
3.2  ESTIMATES OF ORGANIC EMISSIONS
     A modeling approach based on applicable mass transfer equations was
selected as the method of estimating organic emissions from TSDF.  Models
initially developed by the EPA Office of Solid Waste were refined to incor-
porate inputs relevant to estimating air emissions.  The models selected
for use are formulated for individual management processes at TSDF and
account for such factors as process design and operating parameters as well
as the meteorological effects on emissions.  These emission models were
used to generate estimates of the amounts of organics in the incoming
                                   3-18

-------
wastes that are emitted to the air or biodegraded during processing.  More
traditional emission estimating techniques and methodologies, such as
basing emission estimates on the results of a limited number of actual TSDF
source tests, are not appropriate for the diverse operations found in this
industry.  The TSDF industry and its waste management processes are too
varied to use source test data as the sole basis to estimate industry-wide
emissions.
     The use of emission models makes it possible to generate emission
estimates under a wide variety of source conditions and waste compositions.
The accuracy of estimates made by the emission models in comparison to
actual field measurements of emissions for specific sites has been exam-
ined.  That comparison is discussed in Appendix C.  In general, it was
found that, where comparisons could be made, emission model estimates com-
pared favorably with field data.  Appendix F contains the TSDF source test
data.
     The following sections describe the bases for developing estimates of
organic compound emissions from TSDF using the modeling approach.  Section
3.2.1 discusses the elements necessary for producing nationwide emission
estimates for individual waste management units.  Section 3.2.2 discusses
how those elements are combined in a single computer model to produce the
nationwide emission estimates.
3.2.1  Emission Estimation Data Requirements
     Key elements in the estimation of organic emissions from TSDF are the
availability of:  (1)  facility-specific information, (2) management process
emission characteristics,  and (3) waste compositions.  Facility-specific
information and data include the types of waste management processes pres-
ent in those facilities, the RCRA waste codes managed at the facilities,
and the total quantity of waste managed for each of the facilities nation-
wide.  Some facility-specific information is available through data bases
established for other EPA projects, e.g., the HWDMS, the 1981 Westat Sur-
vey, and the 1986 Screener (refer to Appendix D, Section D.2.1.4, for a
description of how these data sources are used).  Where facility-specific
data such as waste compositions and management process characteristics
(e.g.,  aerated versus  quiescent operations) are insufficient, estimated
                                   3-19

-------
 values  based on existing data bases of  industry-specific waste compositions
 and  operating practices are used.   (See Appendix D, Sections D.2.2 and
 D.2.4,  for waste composition and operating practice discussions, respec-
 tively.)  Section 3.2.2.1 describes the facility information available for
 the  generation of nationwide estimates.
      In addition to facility-specific data, emitting characteristics of the
 waste management units are needed to estimate nationwide emissions.  Typi-
 cally,  emission measurements are made at the source and those measurements
 serve as the basis for characterization of similar emission sources.  In
 the  case of TSDF, there is a diversity of sources and factors within a
 source  that have a significant impact on emissions, waste composition being
 a major one; this variation makes estimation of nationwide TSDF emissions
 directly from only measured data impractical.  Other factors that restrict
 this  approach include the overall lack of emission test data for the range
 of TSDF management processes and the absence of standardized test methods
 that  allow meaningful comparisons of available emission data to be made.
 As an alternative, emission models have been adapted to facilitate genera-
 tion  of waste management process emission estimates.  These emission models
 are presented in Appendix C, Section C.I.  To use the emission models, it
 is necessary to define certain waste management unit design and operating
 characteristics (such as surface area and waste retention time for surface
 impoundments).  Given that this level of detail is not available for most
 facilities, process parameters based on model management units were devel-
 oped  for use in calculating emissions (also, costs of control and emission
 reductions).  Using survey results and information from other sources such
 as design manuals and site visit reports, model units were developed in
 terms of operating and design parameters spanning typical ranges of surface
 area, retention times, and other characteristics representative of the TSDF
 industry.  A sensitivity analysis was conducted for each model to determine
which input parameters, over what range, have significant effects on emis-
 sion model  estimates.  Appendix C,  Section C.2, discusses the sources of
 information and rationale used to develop the TSDF model units and lists
 the specific characteristics of each model waste management unit that are
 needed to compute emissions using the appropriate emission model.
                                   3-20

-------
     The other key element in estimating emissions is the composition of
the waste in the waste management unit.  The specific chemicals found in
each waste management unit nationwide are not known.  However,  facility-
specific data described above do identify RCRA waste codes and  their
management process codes.  Existing data bases of waste compositions are
available by industrial category for waste codes.  These waste  codes allow
the assignment of waste compositions to process codes in order  to estimate
emissions.  These data bases have been combined into a single data base
that contains waste compositions for over 300 SIC codes.  The data base
presents waste composition as a function of SIC, RCRA waste codes, and
their physical/chemical forms.  The file is described briefly in Section
3.2.2.2 and described in detail in Appendix D, Section D.2.2.
     Table 3-4 presents the relative emissions predicted by the emission
models for selected model waste management units.  This table lists pre-
dicted uncontrolled organic emissions by model unit for five different
model waste compositions.  The specific compositions of the five model
wastes are given in Appendix C, Section C.2.2, along with the rationale for
their development.  The results in Table 3-4 illustrate the variability in
emissions that may occur from waste management units for different waste
compositions.  The table also shows emission variability between waste
management units for the same waste type.  No conclusions should be drawn
from this latter comparison without considering the differences in waste
throughput between the waste management units.  It should be pointed out
that, to the extent possible, the composition and quantities of the actual
waste streams processed at the existing facilities were used in estimating
nationwide emissions.  The model wastes are presented here to illustrate
the variability in potential air emissions in relation to waste composition
and management process.
     In calculating nationwide TSDF air emissions, emission models are used
with the model waste management unit design and operating characteristics
to produce emission factors for the model units.  The model unit emission
factors are estimates of the fraction of specific organic compounds enter-
ing the waste management unit that become air emissions from that unit.
Derivation of these emission factors involves combining the steps discussed
                                   3-21

-------
     TABLE  3-4.   SUMMARY  OF  SELECTED MODEL  HAZARDOUS WASTE MANAGEMENT UNIT
       UNCONTROLLED  ORGANIC  EMISSION ESTIMATES  FOR  MODEL WASTES  (Mg/yr)a
Model unit**
Covered storage tank
(S02D) .
Covered quiescent
treatment tank (T01E)
Quiescent uncovered
storage tank (S02I)
Quiescent uncovered
treatment tank (T01B)
Quiescent storage
impoundment (S04C)
Quiescent treatment
impoundment (T02D)
Quiescent disposal
impoundment (D83A)
Uncovered aerated/

Aqueous
sludge/
slurry
0.117
0.24
24
34
686
946
842
870
Model
Dilute
aqueous
2.12
4.6
8.1
19
159
269
130
130
waste
Organic
liquid
0.437
1.19
514
954
--
—
—
_ _
type
Organic
s;ludge/
slurry
1.11
1.40
586
1,026
--
--
--
_ _

Two-phase
aqueous/
organic
0.891
1.94
9.7
31
183
326
16,000
— _
  agitated treatment
  tank (T01G)

Aerated/agitated treat-
  ment impoundment
  (T02J)
1,920
390
Waste fixation (Fixation   4,110
  Pit B)

Drum storage (S01B)       0.0036

Dumpster storage (S01C)     0.72

Wastepiles (S03E)          139.7
        0.0000909
       0.0236    0.0298

        0.049      1.44
     380



  31,700


0.000181



     100
                                                                   (continued)
                                    3-22

-------
                            TABLE 3-4 (continued)
Model unitb
Landfill-active (D80E)
Landfill -closed (D80H)
Land treatment (D81C)

Aqueous
sludge/
slurry
358C
0.068
269
Model waste type
Organic
Dilute Organic sludge/
aqueous liquid slurry
—
—
21.6

Two-phase
aqueous/
organic
29QC
2.09
--
— = Indicates this model unit does not manage this model waste type, thus an
     uncontrolled emission estimate is not available.

aThis table lists the estimated organic emissions for selected model waste
 management units when the listed model wastes are managed in those units.
 The model unit definitions are given in Appendix C, Section C.2.1.  The
 model waste compositions are also described in Appendix C, Section C.2.2.
 These compositions and resulting emission estimates are not intended to be
 representative of nationwide TSDF operations but rather are presented to
 illustrate the variability in potential air emissions in relation to the
 waste composition and management process.
     parenthetical listings are the model unit designations under which the
 model unit definitions can be found in Appendix C, Section C.2.2.

cThis estimate does not assume that regulations restricting land disposal of
 bulk liquids are in effect.
                                    3-23

-------
 previously  in  this  section with  a  knowledge of the properties of the com-
 pounds  for  which  emission factors  are  required.  The development of emis-
 sion  factors is explained in detail  in Appendix D, Section D.2.4.
 3.2.2  Nationwide TSDF  Emissions
      Nationwide organic air emissions  from the TSDF industry were estimated
 using the Source  Assessment Model  (SAM), a computerized simulation program
 designed to generate  nationwide  emissions estimates on a facility, waste
 management  unit,  or emission source  basis.  Summation of individual facil-
 ity results provides  the nationwide  emission estimate.  The SAM utilizes a
 variety of  information  and data  concerning the TSDF industry to calculate
 emissions.  The SAM processes the  information and data from a number of
 input files that  contain TSDF-specific information (facility location,
 waste management  processes used, and types and quantities of wastes man-
 aged),  waste characterization data (approximate compositions of typical
 wastes), and air  emission model  estimates (emission factors based on char-
 acteristics of both TSDF waste management units and waste types).
      Because of the complexity of the TSDF industry and the current lack of
 detailed information  for all TSDF, it  is unlikely that the SAM estimates
 are accurate for  an individual facility.  However, it is believed that the
 SAM emission estimates  are a reasonable approximation on a nationwide basis
 and the TSDF modeling approach provides the best basis for analysis of
 options for controlling TSDF air emissions.
      A brief discussion of the input data files, assembled for and used by
 the SAM to  calculate  air emissions, and the output emissions files gen-
 erated by the SAM are presented in the following sections of this chapter.
 Figure 3-6  outlines the main SAM files and functions used in estimating
 nationwide  emissions from the TSDF industry.  The SAM, its data inputs and
 outputs, and the overall logic used in the model's calculations are dis-
 cussed in more detail  in Appendix D.
     3.2.2.1  SAM Input Files.  There are four main data files that are
 inputs to the SAM nationwide uncontrolled emission estimates:  the Industry
 Profile (a  file of waste management practices for each TSDF in the Nation),
the waste characterization file (also referred to as the Waste Characteri-
zation Data Base), the chemical properties file, and the emission factors
                                   3-24

-------
 INPUT FILES
                                                                        OUTPUT
   Industry
    Profile
    Waste
Characterization
     File
   Chemical
  Properties
     File
   Emission
    Factors
     File
   SAM
Processor
Nationwide TSDF
  Uncontrolled
   Emissions
    Figure 3-6. Source Assessment Model (SAM) input files used in estimating nationwide
        treatment, storage, and disposal facilities (TSDF) uncontrolled air emissions.
                                      3-25

-------
 file.   These  inputs  provide the  information  and data necessary to calculate
 nationwide TSDF  uncontrolled  emissions.
     3.2.2.1.1   Industry  Profile.   The  Industry Profile data base was
 developed to  provide a  list of TSDF nationwide and to describe facility-
 specific waste management practices in  terms of the types and quantities of
 wastes  handled and the  processes utilized.   Several hazardous waste indus-
 try surveys and  data bases, available through EPA's Office of Solid Waste,
 serve as the  basis of the SAM Industry  Profile (see Appendix D, Section
 D.2.1).  The  information  and  data from  each  of these surveys and data bases
 were used in  the SAM to estimate nationwide  emissions and impacts of poten-
 tial control  options.
     The information that the SAM uses  from  the Industry Profile to esti-
 mate nationwide  emissions includes  the  following for each TSDF:  (1) facil-
 ity identification number (FCID), (2) location coordinates of the facility,
 (3) the primary  SIC  code for  the facility, (4) the RCRA waste codes managed
 at the TSDF,  (5) the waste quantity for each of the waste codes, and
 (6) the management process codes applicable  to each waste code.  It is
 important to  note that  the SIC and  waste codes link the facility to the
 waste characterization  file,  which  gives estimated waste compositions.
     3.2.2.1.2   Waste characterization  file.  This waste characterization
 file contains waste  data that have  been compiled to represent chemical-
 specific waste compositions for each waste found within an SIC code.  An
 RCRA waste may be generated in one  of several physical/chemical forms; for
 example, a waste may be an aqueous  liquid or an organic sludge.  The waste
 characterization file contains the  composition of waste streams in terms of
 chemical constituents and their respective concentrations for each physi-
 cal/chemical  form of a waste  associated with a particular RCRA waste, code..
 in an SIC category.   If specific chemical constituents were not found in
 the original  data, chemical  assignments were made based on a review of
 similar TSDF  processes.  Wherever available, specific chemicals were
 retained in the waste characterization file.  The data provided in the
waste characterization file are accessed by the SAM for each TSDF emission
calculation.  (See Appendix D, Section D.2.2, for a more detailed discus-
sion.)
                                   3-26

-------
     3.2.2.1.3  Chemical properties file.  Emission estimation for each of
the more than 4,000 waste chemical constituents identified in the waste
characterization file would require property data for all compounds; many
of which are not available.  Therefore, to provide the emission models with
appropriate constituent physical,  chemical, and biological properties, the
waste constituents were categorized and grouped into classes based on
volatility (i.e., vapor pressure or Henry's law constant) and
biodegradation.  These categories were defined to represent the actual
organic compounds that occur in hazardous waste streams and serve as
surrogates for the particular waste constituents in terms of physical,
chemical, and biological properties in the emission calculations carried
out by the SAM.  (See Appendix D,  Section D.2.3, for a more detailed
discussion.)
     3.2.2.1.4  Emission factors file.  For each waste management process
(e.g., aerated surface impoundment or treatment tank), the respective emis-
sion models applicable to the process were used to determine the amount or
fraction of the organic compound entering the unit that is emitted to the
air and the fraction that is biodegraded.  The calculations were made for
each chemical surrogate category for each waste management process.  In
addition to emission factors for process-related emissions, emission fac-
tors developed for transfer and handling-related emissions were also incor-
porated into the SAM program file.  The emission factors used for estimat-
ing TSDF emissions in this document were calculated using the TSDF air
emission models as presented in the March 1987 draft of the Hazardous Waste
Treatment, Storage, and Disposal Facilities:  Air Emission Models, Draft
Report.16  since that time, certain TSDF emission models have been revised.
A new edition of the air emission models report was released in December.
1987.17  7he principal changes to the emission models involved refining the
biodegradation component of the models for biologically active systems
handling low organic concentration waste streams.  With regard to emission
model outputs, the changes from the March 1987 draft to the December 1987
version affected, for the most part, only aerated surface impoundments and
result in a minor increase in the fraction emitted for the chemical
surrogates in the high biodegradation categories.18  For the other air
emission models, such as the land treatment model, which were also revised
                                   3-27

-------
to incorporate new biodegradation rate data, the changes did not result in
appreciable differences in the emission estimates.  Since the December 1987
report version was issued, new data on biodegration rates have been
obtained and comments were received.19  Based on these data and comments,
the biodegradation model for aerated wastewater treatment systems was
further revised to incorporate Monod kinetics.  Additional investigation
and comments led to an evaluation of changes to the model units used for
aerated tanks and impoundments.  These changes improve the technical basis
for the biodegradation model.  However, the combined effect of these
changes did not significantly affect the estimated nationwide emissions and
other impacts presented in this document.20  Therefore, the emission
factors remain based on the March 1987 draft of the air emissions model
report and the model unit definitions were not changed.   (Appendix C,
Section C.I.1.1.3, contains more details on the biodegradation modeling and
Appendix D, Section D.2.4, contains a more extensive discussion of emission
factors.)
     3.2.2.2  Uncontrolled Nationwide Emissions.  The SAM computes nation-
wide uncontrolled TSDF emissions by first identifying particular waste
management process units within the facility from the Industry Profile.
Once a management process is identified, the SAM then calculates emissions
on a chemical-by-chemical basis.  The quantity of a particular chemical in
the waste stream is multiplied by the appropriate emission factor, which is
determined by the chemical, physical, and biological properties of the
chemical.  Emissions for the unit are the sum of the emissions for each
chemical constituent in the waste stream.  Emissions for each management
process unit can then be summed; emissions from source categories  (manage-
ment units with similar emission characteristics, e.g., quiescent storage.
impoundments and quiescent treatment impoundments) are then summed to yield
a nationwide emission estimate.
     The nationwide emission estimates for the current TSDF community are
based on 1985 data containing general operating conditions and practices,
the time covered by the most recent TSDF industry survey.  These emission
estimates are considered to represent the uncontrolled situation or case;
review of the existing applicable State regulations has shown a wide varia-
tion in level of control required for these sources, with many States
having no control requirements for TSDF.

                                   3-28

-------
     The uncontrolled nationwide TSDF emission estimate as determined by

the SAM is 1.8 million Mg of organic emissions annually.  The breakdown of

nationwide emissions by source category is provided in Table 3-5.  (Chap-

ter 6.0 presents additional information on these uncontrolled emissions.)

Table 3-5 shows that storage tanks are estimated to be the single largest

emitting source nationwide.  Treatment tanks and impoundments that are

aerated to promote biological activity are the second highest single

source.  These two source categories combined account for about 70 percent

of the annual emissions estimated.

3.3  REFERENCES

1.   Memorandum from Coy, David, RTI, to Docket.  December 9, 1987.
     Hazardous waste treatment, storage, and disposal facility (TSDF) uni-
     verse of waste constituents.

2.   U.S. Environmental Protection Agency.  Summary Report on RCRA Activi-
     ties for May 1986.  Office of Solid Waste.  Washington, DC.  June 16,
     1986.  p. 4.

3.   U.S. Environmental Protection Agency.  The Hazardous Waste System.
     Office of Solid Waste and Emergency Response.  Washington, DC.  June
     1987.  p. 1-4.

4.   Westat,  Inc.  National Survey of Hazardous Waste Generators and Treat-
     ment, Storage and Disposal Facilities Regulated Under RCRA in 1981.
     Prepared for the U.S. Environmental Protection Agency, Office of Solid
     Waste.  April 1984.  p. 141.

5.   Reference 4, p. 65.

6.   Reference 3, p. 2-3.

7.   Reference 2, p. 4.

8.   Abt Associates, Inc.  National Small Quantity Hazardous Waste Genera-
     tors Survey.  Prepared for the U.S. Environmental Protection Agency,
     Office of Solid Waste.  Washington, DC.  February 1985.  p. 2.

9.   Reference 8, p. 2.

10.  Reference 4, p. 69.

11.  Reference 2, p. 4.

12.  Code of Federal Regulations.  Title 40, Part 260.10.  Definitions.
     U.S. Government Printing Office.  Washington, DC.  July 1, 1986.
     p. 340-347.
                                    3-29

-------
   TABLE 3-5.  NATIONWIDE UNCONTROLLED TSDF ORGANIC EMISSION ESTIMATES9
     Source category
Nationwide uncontrolled emissions,
             103 Mg/yr
Drum storage
Dumpster storage
Storage tanks
Quiescent surface impoundments'3
Quiescent treatment tanks
Aerated/agitated tank and surface
  impoundments
Wastepiles
Landfills
Waste fixation
Incineration0
Land treatment
Spills
Loading
Equipment leaks
                 0.19
                78
               756
               209
                48
               515

                 0.13
                40
                 2.1
                 0.88
                73
                 0.43
                 6.8
                80
Total
             1,810
TSDF ~ Treatment, storage, and disposal facility.
aThis table presents the nationwide estimates of uncontrolled TSDF organic
 emissions generated by the Source Assessment Model described in Appendix
 D.  Emissions are presented for management processes that have similar
 emission characteristics, i.e., source categories.
^Includes quiescent surface impoundments used for both storage, treatment,
 or disposal.
cUncontrolled  incinerator emissions includes emissions from wastes that
 are routinely incinerated with stack exhaust gas emission controls.
 These sources are currently regulated under 40 CFR 264 Subpart 0.  The
 uncontrolled  emission scenario does not include wastes that are or would
 be incinerated as a result of implementing the RCRA land disposal
 restrictions  (LDR).  The baseline and two example control strategies do,
 however, account for the incinerator emissions resulting from the LDR.
 The emission  scenarios are explained in Chapter 5.0.
                                   3-30

-------
13.  Memorandum from Maclntyre, Lisa, RTI, to Docket.  November 4, 1987.
     Data from the 1986 National Screening Survey of the Hazardous Waste
     Treatment, Storage, Disposal and Recycling Facilities used to develop
     the Industry Profile.

14.  Memorandum from Maclntyre, Lisa, RTI, to Docket.  November 4, 1987.
     Data from the National Hazardous Waste Data Management System used to
     develop the Industry Profile.

15.  Reference 13.

16.  Research Triangle Institute.  Hazardous Waste Treatment, Storage and
     Disposal Facilities:  Air Emission Models, Draft Report.  Prepared for
     U.S. Environmental Protection Agency.  Office of Air Quality Planning
     and Standards.  Research Triangle Park, NC.  March 13, 1987.

17.  U.S. Environmental Protection Agency.  Hazardous Waste Treatment,
     Storage, and Disposal Facilities (TSDF)--Air Emission Models.
     Research Triangle Park, NC.  Publication No. EPA-450/3-87-026.
     December 1987.

18.  Memorandum from Coy, D., RTI, to Docket.  January 1989.  Investigation
     of and Recommendation for Revisions to Aerated Model Unit Parameters
     Used in the Source Assessment Model.

19.  Chemical Manufacturers Association.  Comments of the Chemical
     Manufacturers Association on the Environmental Protection Agency
     Document "Hazardous Waste TSDF - Background Information for Proposed
     RCRA Air Emission Standards - Volumes I and II."  Washington, D.C.
     July 11, 1988.  105 p.

20.  Reference 18.
                                    3-31

-------

-------
                          4.0  CONTROL TECHNOLOGIES

     A variety of control technologies is available that can be used to
reduce organic air emissions from hazardous waste treatment, storage, and
disposal facilities (TSDF).  All of these control technologies are not
applicable to all TSDF emission sources.  The applicability of a control
technology to a TSDF emission source depends on the type of waste manage-
ment unit as well as the characteristics of the hazardous waste managed in
the unit.  The purpose of this chapter is to introduce the control technol-
ogies that are potentially applicable to TSDF emission sources.  Chapters
5.0 through 7.0 present analyses to evaluate the organic air emission
reductions, health risk and environmental impacts, and costs for implement-
ing alternative combinations of the control technologies to TSDF emission
sources on a nationwide basis.
4.1  APPLICATION OF CONTROL TECHNOLOGIES TO TSDF EMISSION SOURCES
4.1.1  Control Technology Categories
     Control technologies applicable for TSDF organic air emission reduc-
tion can be classified into five major categories:
     •    Suppression controls
     •    Add-on controls
     •    Organic removal and hazardous waste incineration processes
     •    Process modifications
     •    Work practice improvements.
     Suppression controls contain or capture the organics at the TSDF
emission source.  For example, placing a cover on the surface of the waste
contains the organics in the waste medium and inhibits the release of
                                     4-1

-------
organic vapors to the atmosphere.  Installing an enclosed waste management
unit in place of an open unit or erecting an enclosure over an existing
waste management unit captures the organic vapors released from the waste
and allows the control of the vapors using an add-on control device.
     Add-on controls reduce organic air emissions by removing organics from
the captured vapor stream prior to discharge of the gases to the atmos-
phere.  This is achieved by extraction of the organics from the vapor
stream or by destruction of the organics in the vapor stream.
     Organic removal and hazardous waste incineration processes remove
volatile organics from the hazardous waste before the waste arrives at the
next TSDF waste management unit.  These processes offer an alternative to
using add-on controls to control organic air emissions after they have been
emitted from the TSDF unit.  The type of organic removal or incineration
process used varies depending on the hazardous waste forms.
     Process modifications achieve organic air emission reductions by
changing the equipment or procedures used to manage hazardous waste.
     Work practice improvements are steps that the TSDF personnel can
implement during everyday waste management unit operations to minimize
organic air emissions.  For example, programs can be implemented to
promptly detect and repair leaking equipment.
     This chapter presents descriptions of the control technologies that
are potentially applicable to the TSDF emission source categories identi-
fied in Chapter 3.0.  The control technologies are organized using the five
control technology categories described above and presented in the order
listed in Table 4-1.
4.1.2  Organic Air Emission Control Efficiency
     The effectiveness or efficiency of each control technology to. reduce
organic air emissions is a key parameter used for the TSDF control option
analyses presented in Chapters 6.0 and 7.0.  The preferred method for
determining the potential organic air emission control efficiency for a
particular control technology is by the source testing of full-sized
control devices.  Unfortunately, source testing is not practical for
certain types of control technologies because of the large area that must
be enclosed to obtain accurate results or physical conditions that prevent
measurement devices from being placed at the source of the emissions.
                                     4-2

-------
     TABLE 4-1.  TSDF CONTROL TECHNOLOGY CATEGORIES
Suppression controls
     Fixed-roof tanks
     Floating roof tanks
     Pressure tanks
     Floating membrane covers
     Air-supported structures
     Flexible membrane covers
     Rigid membrane covers
     Rigid structures
Add-on controls
     Carbon adsorbers
     Thermal vapor incinerators
     Catalytic vapor incinerators
     Flares
     Boilers and process heaters
     Condensers
     Absorbers
Organic removal and hazardous waste, incineration processes:

     Steam stripping units
     Air stripping units
     Thin-film evaporation (TFE) units
     Batch distillation units
     Dewatering units
     Hazardous waste incinerators
Process modification

   • Coking of petroleum refinery sludges
   • Mechanical mixing for waste fixation
   • Submerged loading of containers
   • Subsurface injection
Work practice modification

   • Leak detection and repair
   • Drum storage area housekeeping
                           4-3

-------
Consequently, the control efficiency must be estimated using information
such as laboratory test data and mathematical models.
     This chapter discusses the organic air emission control efficiencies
that each control technology is capable of achieving when applied to TSDF
emission sources.  The source test data used to determine the control
efficiencies for many of the control technologies are summarized in Appen-
dix F.  Appendix H presents detailed descriptions of the methodology and
calculations used to determine the control efficiencies for the control
technologies for which no source test data could be obtained.
4.1.3  Secondary Air and Cross-Media Impacts
     The control technologies applicable to TSDF emission sources achieve
organic air emission reductions by using physical, chemical, and thermal
processes that may create additional environmental impacts.  The impacts
resulting from the emission of non-organic air pollutants are termed
"secondary air impacts."  The impacts from production of new liquid or
solid wastes are termed "cross-media impacts."
     Control technologies based on extraction processes remove the volatile
organics in the form of liquid or solid by-products.  Often these
by-products can be recycled or burned as a fuel.  However, in some situa-
tions, there is no other alternative but to dispose the by-products as
wastes, thereby creating additional demands on wastewater treatment units
and landfills.  Control technologies based on destruction processes convert
organic vapors to carbon dioxide, water, and small quantities of various
other chemical compounds.  Depending on the original organic composition in
the waste, non-organic air pollutants may be formed that need to be con-
trolled.  Supplying electricity and process steam required to operate
certain TSDF control technologies may create air emissions, wastewater
discharges, and solid wastes from non-TSDF sources such as industrial
boilers and utility power plants.
     Because a control technology may produce secondary air and cross-media
impacts, the human health and environmental benefits from the organic air
emission reduction that can be achieved by applying the control technology
to TSDF emission sources are evaluated relative to the secondary air and
cross-media impacts produced by implementing the control technology.  This
                                     4-4

-------
chapter identifies the types of secondary air and cross-media impacts
associated with each of the control technologies.  Chapter 6.0,  Section
6.3, presents the results of the secondary air and cross-media impacts
analysis.
4.2  SUPPRESSION CONTROLS
     Suppression controls consist of covers and enclosures.  These controls
serve to keep the volatile organics in the hazardous waste process streams
instead of being released to the atmosphere.  However,  the potential
remains that the volatile organics in the waste could ultimately be
released to the atmosphere from a point downstream in the storage, treat-
ment, or disposal of the waste unless suppression controls are used in
conjunction with add-on control, organic removal, or process modification
control technologies.
     Covers that directly contact the waste medium suppress the volatiza-
tion of the organics by creating a physical barrier at the waste surface.
There is no or very little vapor space between the waste surface and the
underside of the cover where volatile organic vapors can collect.  The
effectiveness of a cover in suppressing organic air emissions depends on
the permeability of the cover, the leak rate at the cover edges and from
any fittings on the cover, and the frequency that the cover is opened to
add or remove material from the waste management unit.
     Organic air emissions can also be suppressed by forming a closed vapor
space above the waste surface.  Enclosing the vapor space can be achieved
by erecting a structure around the entire waste management unit or, for
some types of open-top units, installing a rigid cover.  The organic vapors
from the waste are confined by the enclosure and prevented from being
emitted to the atmosphere.  However, if the enclosure vents directly to the
atmosphere, the enclosure suppression effectiveness will be diminished
significantly.  Therefore, many types of enclosures must be used in
combination with an add-on control device to provide effective TSDF organic
air emission control.
4.2.1  Fixed-Roof Tanks
     A fixed-roof tank is a vertical cylindrical steel  wall tank with a
cone-shaped or dome-shaped roof that is permanently attached to the tank
                                     4-5

-------
shell (see Figure 4-1).1  Vents are installed on the roof to prevent the
tank internal pressure from exceeding the tank design pressure limits and,
thereby, causing physical damage or permanent deformation to the tank
structure.  The vents can either open directly to the atmosphere, be
equipped with valves that open at specified pressure or vacuum settings, or
be connected to an add-on control device (e.g., carbon adsorption system,
vapor incinerator).
     Storage or treatment of organic-containing liquid or sludge wastes in
fixed-roof tanks instead of open-top tanks reduces organic air emissions.
By covering the tank, the waste surface is sheltered from the wind.  This
decreases the mass transfer rate of organic compounds in the waste to the
atmosphere.  The extent to which organic air emissions are reduced varies
on many factors including waste composition and concentrations, windspeed,
and the ratio of the tank diameter to the depth of the liquid contained in
the tank.
     Theoretical and empirical models have been developed to study open-top
and fixed-roof tank emissions.  Several of these models were selected for
the TSDF analyses and are described in Appendix C, Section C.I.I.  Using
the models, estimated organic air emission from a 76 m3 (20,000 gal) open-
top tank were compared to an equivalently sized fixed-roof tank storing the
same type of waste material.  This analysis is described in Appendix H,
Section H.2.1.  For a windspeed of 4.5 m/s (10 mph), the estimated organic
air emissions from the fixed-roof tank are 86 to 99 percent lower than the
open-top tank emissions depending on waste composition.  Thus, using fixed-
roof tanks in place of open-top tanks can provide significant suppression
efficiencies.
     An existing open-top tank can be converted to a fixed-roof tank by
retrofitting the tank with a dome roof.  Aluminum, geodesic dome roofs are
available from several manufacturers.2,3  These domes have been used suc-
cessfully to cover petroleum and chemical storage tanks.  The domes are
clear-span, self-supported structures (i.e.,  require no internal columns be
placed in the tank) that can be installed on open-top tanks ranging in
diameter from 5 to over 100 m (15 to over 330 ft).
                                     4-6

-------
                                               Eaccb
  Maahol*
 Hoizl. (For
        fill
or dr*lnaz«)
                   Typical  fixed roof tank.
                                                               External  floating roof tank.
                                                                                           7«ne
                                                          7csc—•
Kanhol*
                                                       Manhole
                                                         Rla Plmt«
                                           Support Col
                                        with Caluan
                 Contact Deck Type
            l—'          /         \   \. TanK support Calix
                       /          \      with Coluaa v«l
            £jt ?oacooo* —J           \
                                   ^ 7«por Spac*



                    Noncontact Deck Type
                                      Internal floating roof tanks.


                                  Figure 4-1.  Storage tank covers.
                                                 4-7

-------
     Although fixed-roof tanks provide large reductions in organic air
emissions from open-top tanks, fixed-roof tanks still  can emit significant
quantities of organics.  The major sources of organic  air emissions from
fixed-roof tanks are breathing losses and working losses.4  Breathing
losses occur from the expulsion of vapor through the roof vents because of
the expansion or contraction of the tank vapor space resulting from daily
changes in ambient temperature or barometric pressure.  These emissions
occur in the absence of any liquid level change in the tank.  Working
losses occur from the displacement of vapors resulting from filling and
emptying of the tank.
     Breathing and working losses from fixed-roof tanks can be reduced by
installing an internal floating roof, connecting the tank roof vents to an
add-on control device, or installing pressure-vacuum relief valves on the
tank roof vents.  The use of internal floating roofs in fixed-roof tanks is
discussed in Section 4.2.2.
     For add-on control applications, vapors are contained in the tank
until the internal tank pressure attains a preselected level.  Upon
reaching this level, a pressure switch activates a blower to collect the
vapors from the tank and transfer the vapors through piping to the add-on
control device.  As a safety precaution, flame arresters normally are
installed between the tank and control device.  Other safety devices may be
used such as a saturator unit to increase the vapor concentration above the
upper explosive limit.  Add-on control devices for organic vapors are
discussed in Section 4.3.
     Fixed-roof tanks can be designed to operate safely at internal
pressures up to 35 kPa (2.5 psig).5  The use of pressure relief valves to
control organic air emissions from a 38 m^ (10,000 gal) fixed-roof tank
storing volatile organic liquids has been investigated using emission
models.6  This analysis estimated that using pressure relief valves set at
35 kPa reduces breathing and working losses from a fixed-roof tank storing
high-volatility organic liquids by 20 to 45 percent.  However, many
existing fixed-roof tanks are designed to operate at atmospheric pressure
and cannot be pressurized.  Therefore, use of high-pressure relief valve
                                     4-8

-------
settings for organic air emission control is limited to tanks specifically
built to design specifications for operating at elevated internal
pressures.
     Fixed-roof tanks require no energy to operate.  Use of fixed-roof
tanks at TSDF produces no secondary air or cross-media impacts.
4.2.2  Tank Floating Roofs
     Floating roofs are used extensively in the petroleum refining,
gasoline marketing, and chemical manufacturing industries to control
organic air emissions from tanks storing volatile organic liquids.  A tank
floating roof is basically a disk-shaped structure (termed a "deck") with a
diameter slightly less than the inside tank diameter that floats freely on
the surface of liquid stored in the tank.  A seal is attached around the
outer rim of the deck to cover the open annular space between the deck and
inside tank wall.  The seal mechanism is designed to slide against the tank
wall as the liquid level in the tank is raised or lowered.  There are two
general types of tank floating roofs: external floating roofs and internal
floating roofs.
     Floating roofs are appropriate for TSDF hazardous waste storage tanks
and certain treatment tanks where the presence of the floating cover would
not interfere with the treatment process.  Treatment tanks equipped with
surface mixing or aeration equipment cannot use floating roofs.  Also,
because floating roofs are in direct contact with the hazardous waste, the
materials selected to fabricate the deck and seals must be compatible with
the waste composition.  This may prevent the use of floating roofs in tanks
containing certain types of hazardous waste (e.g., highly corrosive
wastes).
     An external floating roof consists of a single- or double-layer steel
deck that moves within the walls of an open-top tank (see Figure 4-1).7
Pontoon sections often are added to the deck to improve floatation
stability.  Because the top surface of the deck is exposed to the outdoors,
the external floating roof design must include additional components for
rainwater drainage and snow removal to prevent the deck from sinking, and
for cleaning the inside walls of the tank above the deck to protect the
sliding seal mechanism from dirt.  A variety of seal types (e.g., metallic
                                     4-9

-------
shoe seal, liquid-filled seal, or resilient foam-filled seal)  and seal
configurations (e.g., mounted above liquid surface,  mounted on liquid sur-
face) can be used for external floating roofs.8  Small openings are
required on the deck for various fittings such as vents, inspection
hatches, gage wells, and sampling ports.
     An internal  floating roof consists of a steel,  stainless  steel,
aluminum, or fiberglass-reinforced plastic deck that is installed inside a
fixed-roof tank (see Figure 4-1).9  Many internal floating roof designs can
be retrofitted into existing fixed-roof tanks.  Because the fixed roof
shelters the deck from weather, internal floating roofs do not need addi-
tional components for rainwater drainage or for seal protection.  An
internal floating roof is equipped with the same types of deck fittings
used on an external floating roof, but normally uses a simpler deck seal
mechanism (e.g.,  a single resilient foam-filled seal or wiper seal).10
Vertical guide rods are installed inside the tank to maintain  deck align-
ment.  The internal tank space above the deck must be vented to prevent the
accumulation of a flammable vapor mixture.
     Floating roof tanks significantly reduce but do not eliminate organic
air emissions.  Organic vapor losses termed "standing losses"  occur at the
deck seals and fitting openings.  The imperfect fit of the deck seals
allows gaps that expose a small amount of the liquid surface to the atmos-
phere.  Small quantities of vapors that collect in the small openings under
the deck can leak from the deck fitting openings.  Standing losses can be
reduced by installing secondary deck seals, selecting appropriate pressure-
relief valve settings, and using tight-gasketed and bolted covers on all
other fittings.  Additional organic vapor losses termed "withdrawal losses"
occur from evaporation of the liquid that wets the inside tank wall as the
roof descends during emptying operations.
     No emission source test studies of full-sized tanks equipped with
floating roofs have been conducted because of the complexity of erecting an
enclosure around a tank.  However, emission test studies of full-sized
floating roof components sponsored by the American Petroleum Institute
(API) were conducted using a pilot-scale tank.11  The results of these
studies in combination with other data have been used by API and EPA to
                                    4-10

-------
develop empirical models that estimate external and internal floating roof
tank standing and withdrawal losses.12
     For the development of volatile organic liquid storage New Source
Performance Standards (NSPS), EPA analyzed the emission reduction effec-
tiveness of using floating roof tanks compared to fixed-roof tanks using
the empirical models.13  The percentage of reduction in emissions varies
with the tank characteristics (e.g., tank size, vapor pressure of the
material stored in the tank).  A model tank was selected for the NSPS
analysis that has a volume of 606 m3 (160,000 gal), contains a volatile
organic liquid having a vapor pressure of 6.9 kPa (1 psia), and operates
with 50 turnovers per year.  The analysis concluded that, depending on the
type of deck and seal system selected, installing an internal floating roof
tank in a fixed-roof tank will reduce volatile organic emissions by 93 to
97 percent.  The analysis also concluded that a similar level of emission
reduction can be achieved using an external floating roof tank.       %
     Because many tanks at TSDF are smaller than 606 m3 (160,000 gal) and
contain hazardous wastes having vapor pressures less than 6.9 kPa (1 psia),
a separate analysis was performed to estimate the effectiveness of using
internal floating roofs to suppress TSDF organic air emissions.  A detailed
description of this analysis is presented in Appendix H, Section H.2.1.
For this analysis, the model tank capacity of 76 m3 (20,000 gal) was used
with five different waste compositions that are representative of the range
of hazardous wastes managed at TSDF.  Installing internal floating roofs is
estimated to reduce TSDF fixed-roof tank organic air emissions by 74 to 82
percent.  Converting an open-top tank to a fixed-roof tank and installing
an internal floating roof is estimated to reduce emissions by 96 to 99
percent.
     Floating roof tanks require no energy to operate.  Use of floating
roof tanks at TSDF produces no secondary air or cross-media impacts.
4.2.3  Pressure Tanks
     Pressure tanks are structurally designed to operate safely at internal
pressures above atmospheric pressure.  Consequently, pressure tanks operate
as closed systems and do not emit organic air emissions at normal storage
conditions or during routine filling and emptying operations.  Pressure-
                                    4-11

-------
relief valves on the tanks open only in the event of improper operation
(e.g. overfilling the tank) or an emergency (e.g., exposure to excessive
heat).
     There are two general pressure tank classes: tanks with internal
pressure operating ranges not exceeding 204 kPa (2 atm) termed "low-
pressure tanks," and tanks with operating pressure greater than 204 kPa
termed "high-pressure tanks".14  The design and shape of the pressure  tank
depends on the internal pressure operating range-.  Fixed-roof tanks can be
designed to operate at pressures up to 35 kPa (2.5 psig).  Above this
pressure, noded spheroid and noded hemispheriod shapes normally are used
for low-pressure tanks.  Horizontal cylinder and spheroid shapes generally
are used for high-pressure tanks.
     Pressure tanks are closed systems and require no energy to operate.
Use of pressure tanks at TSDF produces no secondary air or cross-media
impacts.
4.2.4  Floating Membrane Covers
     Similar to using a fixed-roof tank to manage hazardous waste, placing
a cover over a surface impoundment reduces the release of volatile organics
contained in the waste by preventing waste mixing due to wind blowing
across the unit.  One type of cover available for application to surface
impoundments is a floating membrane cover.  A floating membrane cover  con-
sists of large sheets of synthetic, flexible membrane material that float
on the surface of a liquid or sludge.  Individual, standard-dimension
sheets can be seamed or welded together to form covers applicable to any
size of surface impoundment.
     Floating membrane covers have been used for many years to cover the
surface of potable water reservoirs.  More recently, use of floating mem-
brane covers has been extended to applications that require the cover be
airtight, as in anaerobic sludge lagoons.  One example of a state-of-the-
art floating membrane cover installation is the successful operation since
1987 of a floating membrane cover on a 2.8 ha (7 acre) surface impoundment
used as an anaerobic digester.15,16  jhis cover is required to be airtight
because a vacuum is pulled from under the cover to extract the methane gas
formed by the anaerobic process.  The cover is fabricated from 2.5 mm
                                    4-12

-------
(100 mil) thick high-density polyethylene (HOPE).  Although HOPE is buoyant
in water, foam floats are placed under the membrane sheet to provide addi-
tional floatation and to form channels for collecting the methane.  Two
blowers are used to pull a vacuum (maximum of 0.25 kPa or 1 in. of water
column) under the cover to extract the methane that accumulates in the gas
collection channels.  The collected gas is vented to a system of three
flares.
     Overall performance of the floating membrane cover in airtight
applications as demonstrated by the 2.5 mm HOPE cover described above is
good.  No leaks have occurred in the HOPE seams.  An initial problem with
leaking around access hatch lids on the cover was corrected by installing
positive seal hatch lids.  To prevent the cover from sinking because of
rainwater accumulating on top of the cover, the cover is fabricated with
sufficient excess materials to form troughs that collect rainfall.  Plastic
drainage pipes are placed in the troughs and connected to a pump that is
periodically operated to drain the accumulated rainwater off the cover.
Also, emergency gas vents are installed on the cover to prevent any buildup
of gas under the cover should the gas collection system blowers fail to
operate.  These vents consists of short lengths of open-ended pipes that
extend a short distance below the liquid surface during normal operation.
The liquid seal prevents gases from being discharged through the vent.
Should a sufficient quantity of gas collect under the cover causing the
cover to bulge above the liquid surface, the vent inlet is lifted out of
the liquid, allowing the gas to be vented and the cover to return to its
normal position contacting the liquid surface.
     Surface impoundments used for hazardous waste treatment are exempt
from the RCRA land disposal restrictions (40 CFR Part 268) if the treatment
residues that do not meet specific treatment standards are removed from the
impoundment for subsequent management within 1 yr of placement in the
impoundment.  The application of floating membrane covers to these TSDF
surface impoundments will require that the cover allow for impoundment
cleaning.  Because a floating membrane cover is heavy (e.g., 2.5 mm HOPE
weighs over 2 kg/m^ or approximately 10 ton/acre*?), routine removal of the
entire cover is impractical.  Therefore, waste residues will need ,to be
                                    4-13

-------
removed with the cover in place, requiring a sludge pumping or other type
of system to be installed on the bottom of the impoundment at the same time
the floating membrane cover is installed.  This requirement may prevent the
use of a floating membrane cover for those TSDF surface impoundment appli-
cations where the residues on the impoundment bottom can only be removed by
draining the impoundment and scraping the material out of the impoundment
using heavy construction equipment (e.g., bulldozer, power shovel).
     The application of a floating membrane cover to a TSDF surface
impoundment will require the cover to be made of a material that is resist-
ant to chemical and biological degradation from compounds in the waste
while also having good strength characteristics to resist tearing due to
wind stresses and long-term weather exposure.  Floating membrane covers for
water reservoir and anaerobic digester applications have been fabricated
using HOPE or chlorosulfonated polyethylene (more commonly known as
Hypalon, a registered trademark of E.I. du Pont de Nemours & Co., Inc.) for
the membrane material.  Because these materials have also been used for
lining hazardous waste landfills and surface impoundments, they are candi-
date materials for TSDF surface impoundment floating membrane covers--
provided the material is effective in controlling organic emissions.
     The effectiveness of using a floating membrane cover for organic
emission control is a function of the amount of leakage from the cover
fittings and seams as well as the losses resulting from the permeation of
the membrane material by volatile organic compounds contained in the waste.
The successful application of floating membrane covers to anaerobic sludge
impoundments demonstrates that leakage from fittings and seams can be
reduced to very low levels by using a membrane material with adequate
thickness, installing proper seals on cover fittings and vents, and follow-
ing good installation practices to ensure the seams are properly welded and
to prevent tearing or puncturing the membrane material.  Consequently, for
a properly installed floating membrane cover, the organic emission control
effectiveness is expected to be determined primarily by the permeability of
the cover to the organic constituents in the waste.
     Permeability is a measure of how well a membrane material resists
allowing the organics to pass through the membrane.  Permeation of a
                                    4-14

-------
membrane material is a three-step process that involves the adsorption of
an organic by the material, diffusion of the organics through the material,
and evaporation of the organics on the air side of the membrane.  The
permeability of a floating membrane cover is a function of the organic
composition and concentration of the waste managed in the surface impound-
ment as well as cover materials composition and thickness.
     No source test-data are available to measure the effectiveness of a
floating membrane cover in controlling organic emissions from a surface
impoundment.  However, an indication of the effectiveness of using floating
membrane covers applied to representative TSDF surface impoundments can be
estimated using theoretical mass transfer relationships.  These estimates
suggest that a flexible membrane cover fabricated from HOPE can be an
effective organic emission control for hazardous waste managed in TSDF
surface impoundments.  For example, the organic emission control levels
estimated for a 2.5 mm HOPE floating membrane cover range from approxi-
mately 50 percent to over 95 percent depending on the organic constituents
in the waste and the waste retention time in the surface impoundment.  The
estimate procedure and calculations are described in Appendix H, Section
H.I.2.  This procedure provides only an approximation of the effectiveness
of using floating membrane covers to control organic emissions because
certain assumptions must be made that simplify the actual mass transfer
conditions that occur in surface impoundments.  Improved estimates of the
organic emission control effectiveness of using floating membrane covers
will be possible when the results from ongoing laboratory tests to measure
the organic permeability of potential membrane materials become available.
     The only secondary air or cross-media impacts from application of
floating membrane covers would be any impacts attributed to the intermit-
tent operation of the small electric-powered or gasoline-powered pumps used
to drain rainwater off the cover.
4.2.5  Air-Supported Structures
     An air-supported structure is a plastic-reinforced fabric shell that
is inflated and, therefore, requires no internal rigid supports.  Figure
4-2 shows the major air-supported structure components.18  The structure
shape and support is provided by maintaining a positive interior pressure
                                    4-15

-------
       VINYL-COATED
      POLYESTER BASE
          FABRIC
BIAS HARNESS
 NET SYSTEM
VEHICULAR
AIR-LOCK
        INFLATION/HEATING
             SYSTEM
                  PERSONNEL DOOR
Sources Air Structures  International,  Inc.
         Figure 4-2. Typical air-supported structure.
                     4-16

-------
(i.e., the interior pressure is greater than the external atmospheric
pressure).
     Large electric-motor driven fans are used to blow air continuously or
intermittently through the structure and out a vent system.  The interior
pressure is maintained at a constant 10 to 15 kPa (1.25 to 1.5 inch of
water) for structure inflation.  Adequate air changes are necessary to
prevent the organic vapor concentrations inside the structure from
exceeding the lower explosive limits.  A standby blower system consisting
of internal combustion engine driven fans normally is installed to keep the
structure inflated and ventilated in the event of an electrical power
outage.  The vent system can discharge directly to the atmosphere or be
connected to an add-on control device.
     Large areas can be enclosed by erecting an air-supported structure.
Structures are commercially available ranging in widths from 24 to 91 m (80
to 300 ft) wide and lengths from 24 to 137 m (80 to 450 ft).1^  For larger
areas, a number of modules can be connected together.  Air-supported
structures have been used as enclosures for conveyors and coke ovens, open-
top tanks, and material storage piles.  A 4,000 m3 (1 acre) aerated
wastewater treatment lagoon at a specialty chemical  manufacturing plant has
been covered by an air-supported structure for more than 4 years.20  Thus,
air-supported structures offer good potential as a suppression device for
TSDF surface impoundments that cannot use floating membrane covers (e.g.,
surface treatment impoundments using surface-mounted aeration equipment).
     The fabric used for the air-supported structure depends on the size of
the structure, design requirements (e.g., wind and snow loadings), and type
of chemicals to which the fabric's inner side will be exposed.  Polyvinyl-
fluoride-coated polyester fabric would likely be the material of current
choice for TSDF applications because of the fabric's=good resistance to
deterioration from chemical, weather, or ultraviolet sunlight exposure.
The service life of the fabric ranges from 2 to 12 years depending on the
site-specific conditions.
     Anchoring the air-supported structure likely will be accomplished by
bolting the edges of the fabric to a continuous, grade-level concrete
footing or beam installed around the perimeter of the surface impoundment.
                                    4-17

-------
Entrance into an air-supported structure is through airlocked doors.  These
doors can be sized to allow earth-moving equipment to be used inside the
structure for impoundment cleaning operations.
     The use of air-supported structures to enclose TSDF surface impound-
ments can result in excessive condensation and high temperatures inside the
structure.  An air-supported structure's interior temperatures typically
are 5 to 11 °C (10 to 20 °F) above the ambient temperature.21  Conse-
quently, during hot summer days, temperatures inside an air-supported
structure can exceed 42 °C (110 °F).  Depending on the severity of these
conditions, workers entering the structure may need to follow additional
safety procedures and be restricted as to the period of time they may
remain inside the structure.  Also, any equipment operating inside the
structure may require more frequent repair or replacement because of
accelerated rust and corrosion of the equipment components.
     The effectiveness of an air-supported structure in controlling organic
air emissions primarily depends on the amount of leakage from the structure
and whether the structure vent system is connected to an add-on control
device.  Air-supported structure leaks are usually confined to areas around
airlocks, doors, and anchor points.  Leak checks were performed at the air-
supported structure operating at the specialty chemical manufacturing plant
(refer to Appendix F, Section F.2.1.1).  A soap solution was sprayed around
the structure base and fittings to locate leaks, and measurements were made
using a portable hydrocarbon analyzer.  Few leaks were found, and the sizes
of the leaks ranged from 2 to 40 ppm.  The operating experience at this
facility indicates that proper installation and maintenance of the air-
supported structure can limit leakage to very low levels.
     Because of the very low leakage levels attainable, almost all of the
organic vapors contained by an air-supported stricture will be ultimately
discharged through the structure's vent system.  Therefore, connecting the
vent system to one of the add-on control devices discussed in Section 4.3
will result in an overall organic air emission control efficiency for TSDF
applications using an air-supported structure that is approximately equiva-
lent to the efficiency of the control device.  These add-on control devices
are capable of achieving control efficiencies in excess of 95 percent.
                                    4-18

-------
     Operation of an air-supported structure consumes large quantities of
electricity to maintain the positive interior pressure.  For example, the
existing air-supported structure covering a 4,000 m3 aerated wastewater
treatment lagoon uses fans with a combined power rating of 26 kW (35 hp)
for structure inflation and ventilation.22  Annual electricity consumption
to operate continuously a standard 26 kW fan is approximately 250,000 kWh.
Application of air-supported structures to TSDF emission sources increases
demand for electricity and, consequently, would contribute to nationwide
electricity consumption impacts.
     Any other air emissions, wastewater effluents, or solid wastes
associated with the use of air-supported structures at TSDF, are determined
by the type of add-on control device used in conjunction with the enclo-
sure.  Add-on control device secondary air and cross-media impacts are
discussed in Section 4.3.
4.2.6  Flexible Membrane Covers
     The flexible membrane cover is the analogous organic suppression
control to the floating membrane cover (described in Section 4.2.4) but for
application to wastepiles.  A flexible membrane cover is simply a large
sheet of a synthetic, flexible membrane material that is placed over the
top of a wastepile.  Like a floating membrane cover, individual, standard-
dimension sheets of the membrane material can be seamed or welded together
to form covers applicable to large wastepiles.  The cover can be secured  at
the perimeter using earth fill or another type of mechanical anchoring
system (e.g., cables attached to concrete piers).  To obtain access to the
waste for addition or removal of material, the entire cover is lifted off
the wastepile or a section of the cover is folded back.
     The material used to fabricate a flexible membrane cover to TSDF
applications needs to be resistant to chemical and biological degradation
from compounds in the waste while also having good strength and durability
characteristics to withstand the wear and tear of repeated handling and
weather exposure.  No source test data are available to measure the effec-
tiveness of a flexible membrane cover in controlling organic emissions from
a wastepile.  The effectiveness of the flexible membrane cover in control-
ling organic emissions is expected to be similar to that of a floating
membrane cover.
                                    4-19

-------
      Flexible membrane covers  require no energy to operate.  Use of
 flexible membrane covers at TSDF produces no secondary  air or cross-media
"impacts.
 4.2.7  Rigid Membrane Covers
      Rigid membrane covers consist of plastic-reinforced  fabric that is
 stretched over  a rigid structural support system  such as  an aluminum frame
 or  a  mast with  tensioned cables.23  The fabric is supported above the waste
 material so that a vapor space is formed between  the waste surface and the
 cover.  Used with an add-on control device, this  type of  cover provides an
 alternative to  an air-supported structure for a TSDF surface impoundment.
      Any non-organic air emissions, wastewater effluents, or solid wastes
 associated with the use of rigid membrane covers  at TSDF  is determined by
 the type of add-on control device used in conjunction with the cover.  Add-
 on  control device secondary air and cross-media impacts are discussed in
 Section 4.3.
 4.2.8  Rigid Structures
      A  rigid structure is a permanent building that is  designed to confine
 air emissions from storage or  processing operations.  The configuration and
 design  of the building depend  on the process requirements and site
 conditions.  Steel-frame construction with metal  or reinforced fiberglass
 panels  most likely would be used for TSDF applications.
      Existing applications of  rigid structures to TSDF  have been for
 particulate matter and odor control from hazardous waste  fixation proces-
 ses. 24,25,26  These buildings  are vented to wet scrubber  control devices.
 Other potential TSDF applications for rigid structures  are to confine air
 emissions from  drum storage and processing operations.
      Any non-organic air emissions, wastewater effluents, or solid wastes
 associated with the use of rigid structures at TSDF is  determined by the
 type  of add-on  control device  used in conjunction with  the structure.  Add-
 on  control device secondary air and cross-media impacts are discussed in
 Section 4.3.
 4.3  ADD-ON CONTROLS
      Add-on controls are processes applied to captured  organic vapors
 vented  from TSDF emission sources.  These controls serve  to reduce organic
                                     4-20

-------
air emissions by destroying organics in the gas stream or extracting
organics from the gas stream before discharging the gas stream to the
atmosphere.  Add-on controls for organic' air emissions are classified into
four broad categories: combustion,  adsorption, condensation,  and absorp-
tion.  General background information about these types of add-on controls
is available in Reference 27.  The type of add-on control best suited for a
particular TSDF emission source depends on the size of the source and the
characteristics of the hazardous waste managed by the TSDF source.
     Combustion destroys the organics in the gas stream by oxidation of the
compounds to primarily carbon dioxide and water.  Because essentially all
organics will burn, combustion add-on controls are applicable to all TSDF
emission sources for which the organic vapors can be captured.  However,
combustion add-on controls will likely be used for those TSDF emission
sources where recovery of the organics is not practical or desirable.
Combustion add-on controls are thermal vapor incinerators, catalytic vapor
incinerators, flares, boilers, and process heaters.
     Adsorption, condensation, or absorption processes can be used to
extract the organics from the gas stream.  All of these processes are
capable of achieving very high levels of organic removal efficiencies.
However, adsorbers or condensers are likely to be less expensive than
absorbers for application to TSDF emission sources.
     The type and magnitude of the secondary air and cross-media impacts
associated with add-on controls varies depending on the type of control.
However, all add-on control devices use electric-motor driven equipment
such as fans, blowers, and pumps.  The electricity required to operate the
control device is supplied by the local electric utility or perhaps an
existing on-site cogeneration unit.  Thus, add-on control device operation
increases demand for electricity, which in turn increases any air, water,
and solid waste impacts associated with the power plants that supply the
electricity.  The types and quantities of these impacts varies depending on
the technology used to generate the electricity (e.g., fossil-fuel-fired
steam boiler, gas turbine, hydroelectric, or nuclear power plants) and, for
combustion power plants, the type of fuel burned (e.g., natural gas, coal,
municipal solid waste).
                                    4-21

-------
4.3.1  Carbon Adsorbers
     Adsorption as applied to air pollutant control is the process by which
organic molecules in a gas stream are retained on the surface of solid
particles.  The solid most frequently used is carbon that has been proc-
essed or  "activated" to have a very porous structure.  This provides many
surfaces  upon which the organic molecules can attach, resulting in a high
rate of organic removal from a gas stream as it passes through a bed of
carbon.
     Activated carbon has a finite adsorption capacity.  When the carbon
becomes saturated (i.e., all of the carbon surface is covered with organic
material), there is no further organic air emission control because all of
the organic vapors pass through the carbon bed.  At this point (referred to
as  "breakthrough"), the organic compounds must be removed from the carbon
before organic air emission control can resume.  This process is called
desorption or regeneration.
     For most air pollutant control applications, regeneration of the
carbon in the adsorber is performed by passing steam through the carbon
bed.  The steam heats the carbon particles, which releases the organic
molecules into the steam flow.  The resulting steam and organic vapor
mixture is condensed to recover the organics and separate the water for
discharge to a wastewater treatment unit.  An alternative method for
regenerating the carbon is to reduce the pressure of the atmosphere
surrounding the carbon particles.  Vacuum regeneration is used for special
carbon adsorber applications when direct recycling of the recovered
organics is desired such as vapor recovery at gasoline tank truck loading
terminals.  A detailed description of carbon adsorption and desorption
mechanisms is available in Reference 28.
     Two types of carbon adsorption systems most .commonly used for air
pollutant control are: fixed-bed carbon adsorbers and carbon canisters.  A
fluidized-bed carbon adsorption system has been developed, but currently is
not commercially available.
     Fixed-bed carbon adsorbers are used for controlling continuous,
organic gas streams with flow rates ranging from 30 to over 3,000 m3/min
(1,000 to over 100,000 ft^/min).  The organic concentration can be as low
                                    4-22

-------
as several parts per billion by volume (ppbv)  or as high as 25 percent of
the lower explosive limit for the vapor stream constituents.  The major
components of a fixed-bed carbon adsorber system are one or more carbon bed
units to adsorb the organics, a condenser to convert the desorbed organics
and steam mixture to a liquid, a decanter to separate the organic and
aqueous phases, and blowers to cool and dry the carbon beds following
desorption.
     Fixed-bed carbon adsorbers may be operated in either intermittent or
continuous modes.  For intermittent operation, the adsorber removes
organics only during a specific period of the day.  Intermittent mode of
operation allows a single carbon bed to be used because it can be
regenerated during the off-line periods.   This mode of operation would be
suitable for TSDF emission sources that operate one 8 to 10 hour shift per
day such as a waste fixation unit. For continuous operation, the unit is
equipped with two or more carbon beds so that at least one bed is always
available for adsorption while other beds are being regenerated.  This mode
of operation would be suitable for TSDF emission sources that are in
operation 24 hours per day such as tanks and surface impoundments.
     Carbon canisters differ from fixed-bed carbon adsorbers.  First, a
carbon canisters is a very simple add-on control device consisting of a
0.21 m^ (55 gal) drum with inlet and outlet pipe fittings (see Figure
4-3).29  A typical canister unit is filled with 70 to 90 kg (150 to 200 Ib)
of activated carbon.   Second, use of carbon canisters is limited to
controlling low volume gas streams with flow rates less than 3 nvVmin
(100 ft3/min).30  Third, the carbon cannot be regenerated directly in the
canister.  Once the activated carbon in the canister becomes saturated by
the organic vapors, the carbon canister must be removed and replaced with a
fresh carbon canister.  The spent carbon canister is then recycled or
discarded depending on site-specific factors.
     For a carbon canister to be an effective organic air emission control
device, the canister must be replaced promptly when carbon breakthrough
first occurs.  An automated, continuous organic analyzer could be used to
signal when carbon breakthrough occurs but is expensive relative to the
total capital cost of the carbon canister unit.  Manual monitoring of
                                    4-23

-------
                         Activated carbon
                         Support material
Figure 4-3.  Carbon canister unit.
           4-24

-------
carbon breakthrough can be conducted by a facility worker checking periodi-
cally to see whether the organic concentration at £he canister outlet has
increased significantly.31  A colorimetric detection test or a portable
instrument that measures organic concentration can be used to check the
canister outlet concentration.  An alternative to monitoring is to replace
the carbon canister regularly based on a maintenance schedule.  The
replacement interval would be a specified number of operating hours less
than the number of operating hours at which carbon breakthrough first
occurs.
     The design of a carbon adsorption system depends on the inlet gas
stream characteristics including organic composition and concentrations,
flow rate, and temperature.  Good carbon adsorber performance requires that
(1) the adsorber is charged with an adequate quantity of high-quality
activated carbon; (2) the gas stream receives appropriate preconditioning
(e.g., cooling, filtering) before entering the carbon bed; and (3) the
carbon beds are regenerated before breakthrough occurs.
     Emission source test data for 12 full-sized, fixed-bed carbon adsorb-
ers operating in industrial applications has been compiled by EPA for a
study of carbon adsorber performance.32  The analysis of these data
concluded that for well-designed and operated carbon adsorbers continuous
organic removal efficiencies of at least 95 percent are achievable over
long periods.  Several units have been shown to continuously achieve
organic removal efficiencies of 97 to 99 percent.
     An equivalent level of performance for carbon canisters applied to
TSDF emission sources is indicated by the results of an emission source
test conducted on carbon canisters installed on the neutralizer tanks for a
wastewater treatment system at a specialty chemicals plant (refer to
Appendix F, Section F.2.2.1.2).  This device was designed for odor control
and not organic removal.  However, 100 percent removal was measured for
1,2-dichlorobenzene, benzene, toluene, chlorobenzene, and chloroform.
Overall organic removal efficiencies measured for various hydrocarbon
categories ranged from 50 to 99 percent.
     High moisture content in the gas stream can affect carbon adsorber
performance for gas streams having organic concentrations less than
                                    4-25

-------
1,000 ppm.33  At these conditions, water molecules compete with the organic
compounds for the available adsorption sites on the carbon particles.
Consequently, the carbon bed working capacity is decreased.  Above an
organic concentration of 1,000 ppm, high moisture does not significantly
affect performance.  Thus, to obtain good adsorber performance for gas
streams with a high relative humidity (relative humidity greater than
50 percent) and low organic concentration (less than 1,000 ppm) requires
preconditioning the gas stream upstream of the carbon bed.  This can be
accomplished using a dehumidification system, installing duct burners to
heat the gas stream, or diluting the gas stream with ambient air.  For TSDF
applications, these gas stream conditions would most likely occur at
locations where a carbon adsorber is used in conjunction with an air-
supported structure enclosing an aerated surface impoundment containing
dilute aqueous hazardous waste.
     Carbon bed operating temperature can also affect carbon adsorber
performance.  Excessive bed temperatures can result due to the release of
heat from exothermic chemical reactions that may occur in the carbon bed.34
Ketones and aldehydes are especially reactive compounds that exothermically
polymerize in the carbon bed.  If temperatures rise too high, spontaneous
combustion will result in carbon bed fires.  To avoid this problem, carbon
adsorbers applied to gas streams containing these types of compounds must
be carefully designed and operated to allow sufficient airflow through the
bed to remove excess heat.
     Carbon adsorption control devices produce two types of cross-media
impacts: (1) wastewater effluent from the condensation of steam used to
regenerate spent carbon; and (2) solid waste from periodic replacement of
spent carbon.  The magnitude of these impacts will depend primarily on the
type of carbon adsorption systems used (e.g., fixed-bed carbon adsorbers.
versus carbon canisters), the type of carbon regeneration used (e.g., steam
regeneration versus vacuum regeneration), and the spent carbon canister
management practices used (e.g., regenerate carbon or direct disposal of
carbon).
     Most fixed-bed carbon adsorbers used for TSDF organic air emission
control are expected to use conventional low-pressure steam regeneration.
                                    4-26

-------
After passing through the carbon bed, the steam is condensed and passed
through a decanter or distillation column to separate the condensed organ-
ics from the water.  A wastewater effluent containing small quantities of
water soluble organics is produced.  Also, the carbon cannot be regenerated
indefinitely.  Gradual deactivation and attrition of the carbon in the
fixed-bed adsorber requires the carbon be replaced with fresh carbon
approximately once every several years.  The spent carbon is either
recycled by returning it to the vendor for processing or discarded in the
appropriate disposal facility as determined by the spent carbon's waste
classification.
     The waste classification of the spent carbon used for air pollutant
control applications will depend on the type of waste managed in the TSDF
unit that is being controlled by the carbon adsorption system.  The spent
carbon from a particular TSDF control application may be determined to be a
hazardous waste if it exhibits any of the four hazardous waste characteris-
tics as defined by the Resource Conservation and Recovery Act (RCRA), Part
261 Subpart C.  If the spent carbon is determined to be nonhazardous, it
may be possible to dispose the carbon in a municipal solid waste landfill
depending on the rules and policies affecting disposal at the landfill.
Otherwise the spent carbon from many TSDF will need to be disposed in a
hazardous waste landfill or incinerator.
     The steam required for fixed-bed carbon adsorber regeneration most
likely will be supplied by an on-site industrial boiler.  Production of the
steam required for regeneration creates secondary air emission impacts due
to the boiler air emissions.  Because natural gas or distillate fuel oil
commonly is the type of fuel burned in industrial boilers, these impacts
primarily are expected to be increases in nitrogen oxides (NOX) and carbon
monoxide (CO) emissions.
     Spent carbon canisters can be either recycled or discarded.35  The
type of spent carbon canister management practice used at a specific TSDF
location will depend on site-specific factors.  Recycling involves removing
the spent carbon from the canister, regenerating the carbon, and then
repacking the canister with regenerated carbon plus any necessary makeup
carbon.  If disposal is selected,  the spent carbon and canister are sent to
an appropriate disposal site depending on the waste classification.
                                    4-27

-------
4.3.2  Thermal Vapor Incinerators
     Thermal vapor incineration is a controlled oxidation process that
occurs in an enclosed chamber.  Figure 4-4 shows a simplified diagram of a
thermal vapor incinerator.  One type of thermal vapor incinerator consists
of a refractory-lined chamber containing one or more discrete burners that
premix the organic vapor gas stream with the combustion air and any
required supplemental fuel.  A second type of incinerator uses a plate-type
burner firing natural gas to produce a flame zone through which the organic
vapor gas stream passes.  Packaged thermal vapor incinerators are commer-
cially available in sizes capable of handling gas stream flow rates ranging
from approximately 8 to 1,400 m3/min (300 to 50,000 ft3/min).36
     Organic vapor destruction efficiency for a thermal vapor incinerator
is a function of the organic vapor composition and concentration, combus-
tion zone temperature, the period of time the organics remain in the
combustion zone (referred to as "residence time"), and the degree of turbu-
lent mixing in the combustion zone.  Field emission testing and combustion
kinetic modeling analyses have been conducted to evaluate thermal vapor
incinerator organic destruction efficiencies.37-41  These analysis results
indicate that thermal vapor incineration destroys at least 98 percent of
non-halogenated organic compounds in the vapor stream at a temperature of
870 °C  (1,600 °F) and a residence time of 0.75 seconds.  If the vapor
stream contains halogenated compounds, a temperature of 1,100 °C (2,000 6F)
and a residence time of 1 second is needed to achieve a 98 percent
destruction efficiency.
     Incinerator performance is affected by the heating value and moisture
content of the organic vapor stream, and the amount of excess combustion
air.  Combustion of organic vapor streams with a heating value less than
1.9 MJ/m3 (50 Btu/ft3) usually requires the addition of supplemental fuel
(also referred to as auxiliary fuel) to maintain the desired combustion
temperature.42  Above this heating value, supplemental fuel may be used to
maintain flame stability.  Although either natural gas or fuel oil can be
used as supplemental fuel, natural gas is preferred.  Supplemental fuel
requirements can be decreased if the combustion air or organic vapor stream
is preheated.
                                    4-28

-------
    o
    CO
                                   0>
               0)

               03
    X
   LU
                     .0

                     U
                     V)
               U
              in
I
Wl
1
IB
'o
                                                    SJ
                                                    I
                                                    o
                                                    •*•*
                                                    CO
                                                    09
                                                    '3

                                                    T3
                                                    U
                                                    s
                                                    
-------
     Thermal vapor incinerator exhaust gases are comprised mainly of carbon
dioxide and water.  Using good thermal vapor incinerator design and operat-
ing practices limits CO and unburned hydrocarbon emissions to very low
levels.  However, the combustion temperature levels required to achieve
good organic vapor destruction efficiency also promote the oxidation of
molecular nitrogen in the combustion air to produce NOX air emissions.
     The quantity of NOX emitted from a thermal vapor incinerator is
affected by peak temperatures in the incinerator combustion zone, quantity
of excess combustion air used for incineration, and period of time combus-
tion gases are exposed to the peak temperatures.  Additional quantities of
NOX can form if the vapor stream contains nitrogen compounds.  A series of
EPA-sponsored source tests on three thermal vapor incinerators used to
control organic emissions from air oxidation plants measured incinerator
outlet NOX concentrations ranging from 8 to 200 ppmv.43  For vapor streams
not containing nitrogen compounds, the measured NOX concentrations were
less than 30 ppmv.
     If compounds containing halogens are present in the organic vapor
stream, hydrogen chloride (HC1) will be formed when the vapors are
incinerated.  Similarly, the presence of sulfur compounds in the vapor
stream results in the formation of sulfur oxides.  These acid gases can be
controlled by venting the thermal vapor incinerator exhaust gases through a
wet scrubber.  Water is normally used as the scrubbing agent increasing the
TSDF wastewater effluent discharge to an on-site wastewater treatment unit
or to a sewer for treatment by a publicly owned treatment works (POTW).  To
meet effluent discharge requirements, it may be necessary to neutralize the
scrubber wastewater prior to discharge to the TSDF wastewater system.  This
is normally accomplished by adding a caustic (e.g., sodium hydroxide) to
the wastewater producing small quantities of salts that must be disposed as
hazardous waste.        .                                    -
4.3.3  Catalytic Vapor Incinerators
     Catalytic vapor incineration is essentially a flameless combustion
process.  Passing the organic vapor stream through a catalyst bed promotes
oxidation of the organics at temperatures in the range of 320 to 650 °C
(600 to 1,200 °F).44  Temperatures below this range slow down or stop the
                                    4-30

-------
oxidation reactions resulting in low destruction efficiencies.   Tempera-
tures above this range shorten catalyst life or may even cause  catalyst
failure.  Oxidation of vapor streams with a high organic content can
produce temperatures well above 650 °C (1,200 °F).  Consequently,  high
organic concentration vapor streams may not be suitable for catalytic
incineration.
     Figure 4-5 shows a simplified diagram of a catalytic vapor incinera-
tor.  The device consists of a chamber where the gas stream vented from the
emission source is heated to the desired reaction temperature by mixing the
organic vapors with hot combustion gas from natural gas-fired burners.  The
heated gas mixture then flows through the catalyst bed.  The catalyst is
composed of a porous inert substrate material that is plated with a metal
alloy containing platinum, palladium, copper, chromium, or cobalt.  A heat
exchanger is installed to preheat the vapor stream and, hence,  reduce the
amount of fuel that must be burned.
     Organic vapor destruction efficiency for catalytic vapor incinerators
is a function of organic vapor composition and concentration, catalyst
operating temperature, oxygen concentration, catalyst characteristics, and
the ratio of the volumetric flow of gas entering the catalyst bed to the
volume of the catalyst bed (referred to as "space velocity").  Destruction
efficiency is increased by decreasing the space velocity.  However, a lower
space velocity increases the size of the catalyst bed and, consequently,
the incinerator capital cost.  For a specific catalyst bed size, increasing
the catalyst bed temperature allows a higher space velocity to  be used
without impairing destruction efficiency.
     A series of studies have been sponsored by EPA to investigate the
destruction efficiency of catalytic vapor incinerators used to  control
organic and hazardous air pollutants.45'46  The results of these studies
concluded that destruction efficiencies of 97 to 98 percent are achievable.
     The destruction efficiency is reduced by the accumulation  of particu-
late matter, condensed organics, or polymerized hydrocarbons on the
catalyst.  These materials deactivate the catalyst by permanently blocking
the active sites on the catalyst surface.  If the catalyst is deactivated,
the volatile organics in the gas stream will pass through the catalyst bed
                                    4-31

-------
(U
                       52


                       m
                       u
                       •^
                       o


                       Z
                       O)
                       
-------
unreacted or form new compounds such as aldehydes, ketones, and organic
acids.  Catalysts can also be deactivated by compounds containing sulfur,
bismuth, phosphorous, arsenic, antimony, mercury, lead, zinc, tin, or
halogens.
     Catalytic vapor incinerators do not have the magnitude of NOX air
emission impacts or potential HC1 and sulfur oxide air emission impacts
associated with thermal vapor incineration because of lower operating
temperatures and applicability restrictions.  Catalytic vapor incinerators'
operating temperatures are significantly lower than the temperatures
required for significant NOX formation from molecular nitrogen in the air
(above 1,600 °C [2,900 °F]).47  Small quantities of NOX may form in the
auxiliary burner flame zone.  Also, the catalysts are very susceptible to
rapid deactivation by halogens or sulfur.  Consequently, catalytic vapor
incineration will not likely be selected to control TSDF organics vapor
streams containing halogen or sulfur compounds.
     Using catalytic vapor incineration does produce small solid waste
impacts.  The incinerator catalyst must be periodically replaced with fresh
catalyst because of gradual deactivation of the catalyst over time.  The
spent catalyst materials are either returned to a catalyst vendor for
recycling or disposed as a solid waste.  Because the catalyst formulations
currently used contain heavy metals, spent catalyst materials will need to
be disposed as a hazardous waste.
4.3.4  Flares
     Unlike vapor incinerators, a flare is an open combustion process.  The
ambient air surrounding the flare provides the oxygen needed for combus-
tion,  Consequently, a flare does not require blowers to provide combustion
air.  To achieve smokeless flare operation, turbulent mixing of the organic
vapor stream with the ambient air at the flame zone boundary can be
"assisted" by injecting steam or air at the flare tip%or by releasing the
gas stream through a high velocity nozzle (i.e., a nozzle with a high
pressure drop).  Flares are used extensively to burn purge and waste gases
from many industrial processes such as petroleum refinery process units,
blast furnaces, and coke ovens.
     Figure 4-6 shows a diagram of a typical steam-assisted flare config-
uration.^  The knockout drum is used to remove entrained liquids from the
                                    4-33

-------
                                                             n«r« Tip
6*1 Calltctton KMd«r
and Transfer L1iw
 I      I
              Knock-out
              On»
                                  StMBNOZZltt
                                                                       Mtot 3urn«rj
                          Onin
                  Figure 4-6. Steam-assisted elevated flare system.
                                        4-34

-------
organic vapor stream.  A water seal is used to prevent air intrusion into
the flare stack.  A pilot burner fired with natural gas is used to ignite
the waste gases.
     Flares without assist continuously burn the vapors from the emission
source.  A flare equipped with a steam, air, or pressure assist operates on
an intermittent basis.  Steam-assisted flares typically are used for burn-
ing large volumes of waste gases released from a process unit during an
upset or emergency condition.  Air-assisted flares are less expensive to
operate than steam-assisted flares.  However, air-assisted flares are not
suitable for large gas volumes because the airflow is difficult to control
when the gas flow is intermittent.  Pressure-assisted flares normally are
used for applications requiring ground-level operation.
     A series of flare destruction efficiency studies has been performed by
EPA.49»50  Based on the results of these studies, EPA concluded that
98 percent combustion efficiency can be achieved by steam-assisted and air-
assisted flares burning gases with heat contents greater than 11 MJ/m3 (300
Btu/ft3).  To achieve this efficiency level, EPA developed a set of flare
design guidelines.51  The guidelines specify flare tip exit velocities for
different flares types and waste gas stream heating values.
     Because flaring is a combustion process, using a flare to destruct
organic vapors also produces NOX emissions.  However, flare NOX emissions
are very low.  Measurements obtained during EPA-sponsored testing of two
flares used to control hydrocarbon emissions from refinery and petrochemi-
cal processes indicate that NOX concentrations in the flared gases are less
than 10 ppmv.52
     Application of flares to TSDF emission sources are not expected to
produce HC1 and sulfur oxide air emission impacts.  Flares are not recom-
mended for organic vapor streams containing halogens or sulfur compounds.
The acid gases formed from these compounds during combustion causes severe
corrosion and premature wear of flare tips.  Thus, flares are not likely to
be selected to control TSDF organic vapor streams containing halogen or
sulfur compounds.
     Steam-assisted flares with high steam rates emit high-pitched sounds
that are considered annoying by many people.  The use of this type of flare
                                    4-35

-------
at a TSDF may create a noise nuisance impact especially if a residential
neighborhood is located near the TSDF.
4.3.5  Boilers and Process Heaters
     A boiler or process heater can be used for organic vapor destruction.
The organic vapor stream is either (1) premixed with a gaseous fuel  and
fired using the existing burner configuration, or (2) fired separately
through a special burner or burners that are retrofitted to the combustion
unit.53  Industrial boilers and process heaters currently are being used  to
burn vent gases from chemical manufacturing and petroleum refining process
units.
     A series of EPA-sponsored studies of organic vapor destruction
efficiencies for industrial boilers and process heaters was conducted by
premixing waste materials with the fuel used to fire representative types
of combustion devices.54,55,56  The destruction efficiency was determined
based on the waste constituent concentrations measured in the fuel feed and
stack gases using a gas chromatograph.  The results of one study indicated
that the destruction efficiency for an industrial boiler firing fuel oil
spiked with polychlorinated biphenyls (PCB) was greater than 99.9 percent.
A second study investigated the destruction efficiency of five process
heaters firing a benzene vapor and natural gas mixture.  The results of
these tests showed 98 to,99 percent overall destruction efficiencies for  GI
to CQ hydrocarbons.
     Industrial boilers and process heaters are located at a plant site to
provide steam or heat for a manufacturing process.  Because plant operation
requires these combustion units to be on-line, boilers and process heaters
are suitable for controlling only organic vapor streams that do not impair
the combustion device performance (e.g., reduce steam output) or reliabil-
ity (e.g., cause premature boiler tube failure).
4.3.6  Condensers
     Condensation is the process by which a gas or vapor is converted to  a
liquid form by lowering the temperature or increasing the pressure.  This
process occurs when the partial pressure for a specific organic compound  in
the vapor stream equals its partial pressure as a pure substance at operat-
ing conditions.  For air pollutant control applications, cooling the gas
stream is the more cost-effective method of achieving organic condensation.
                                    4-36

-------
     There are two major types of condensers:  surface condensers and
contact condensers.  In a surface condenser, the coolant does not contact
the vapors or the condensate.  In a contact condenser, the coolant and
vapor stream are physically mixed together inside the vessel and exit the
condenser as a single stream.  For the TSDF applications, a contact
condenser would not likely be used because the combined organic/coolant
condensate creates additional treatment and disposal requirements.
     A shell-and-tube-type heat exchanger is used for most surface
condenser applications (see Figure 4-7).57  The gas stream flows into a
cylindrical shell and condenses on the outer surface of tubes that are
chilled by a coolant flowing inside the tubes.  The coolant used depends on
the saturation temperature or dewpoint of the particular organic compounds
in the gas stream.  The condensed organic liquids are pumped to a tank.
Additional information about condenser equipment and operations is avail-
able in References 58 and 59.
     The volatile organic removal efficiency for a condenser is dependent
upon the gas stream organic composition and concentrations as well as the
condenser operating temperature.  Condensation can be an effective control
device for gas streams having high concentrations of organic compounds with
high-boiling points.  However, condensation is not effective for gas
streams containing low organic concentrations or composed primarily of low-
boiling point organics.  At these conditions, organics cannot readily be
condensed at normal condenser operating temperatures.
     Appendix F, Section F.2.2.3, summarizes the results of a field
evaluation of a condenser used to recover organics from a steam stripping
process used to treat wastewater at a plant manufacturing ethylene
dichloride and vinyl chloride monomer.  The measured condenser removal
efficiencies for specific organic constituents ranged from a high value of
99.5 percent for 1,2-dichloroethane to a low value of 6 percent for vinyl
chloride.
     Use of surface condensers for TSDF organic air emission control will
likely produce no cross-media or secondary impacts other than any impacts
attributed to electricity consumption.  Because the coolant does not
contact the condensate, organic condensate is not contaminated and can be
                                    4-37

-------
  COOLANT INLET     VAPOR OUTLET
VAPOR INLET
COOLANT OUTLET     CONDENSED ORGANICS
  Figure 4-7. Schematic diagram of a shell-and-tube surface condenser.
                         4-38

-------
readily recycled instead of being disposed.  Electricity is required to
power the coolant and condensate pumps.
4.3.7  Absorbers
     Absorption as applied to air pollutant control is the process by which
organic molecules in a gas stream are selectively removed by a liquid
solvent (referred to as the "absorbent").  This process may occur by a
physical or chemical mechanism.  For physical absorption, the organic
compounds dissolve in the absorbent.  For chemical absorption, the organic
compounds react with the absorbent or with reagents dissolved in the
absorbent.  The combined organic and absorbent mixture is then processed
further to separate the organics and absorbent.
     To achieve high organic control efficiencies using absorption,
intimate mixing of the organic vapors with the absorbent is required.
Several different types of equipment are available that achieve good
contact between the gas and the absorbent.  Absorbers include packed
towers, plate or tray towers, spray towers, and venturi scrubbers.  Back-
ground information about these devices is available in Reference 60.
     The relatively low organic concentrations in the vent streams from
many TSDF emission sources would require long contact times and large quan-
tities of absorbent for effective emission control.  This increases the
size of the absorber vessel required as well as the absorber operating
costs.  Furthermore, the organics and absorbent are physically mixed
together inside the absorber vessel, and exit as a single stream that
creates additional hazardous waste treatment and disposal requirements.
Consequently, application of an absorber to a TSDF emission source is
generally more expensive than using a adsorption, combustion, or condensa-
tion add-on control device.  Thus, it is expected that absorbers will not
be selected for TSDF organic air emission control except perhaps at a TSDF
location where a unique combination of waste characteristics and site-
specific factors make an absorber the better choice for an add-on control
device.
4.4  ORGANIC REMOVAL AND HAZARDOUS WASTE INCINERATION PROCESSES
4.4.1  Steam Stripping
     Steam stripping involves the fractional distillation of volatile
organics from a less volatile waste material.  It is a commercially proven
                                    4-39

-------
process and currently is used to remove organics from dilute aqueous
liquids such as chemical manufacturing process wastewater.  Several
references discuss steam stripping in detail, including a steam-stripping
manual published by EPA,61 discussions of the theory and design proce-
dures,62-65 and discussions of applicability to hazardous wastes.66"69
     The basic operating principle of steam stripping is the direct contact
of steam with the waste, which results in the transfer of heat to the waste
and the vaporization of the more volatile organic compounds.  The vapor is
condensed and separated (usually decanted) from the condensed water vapor.
Final control of organics is accomplished by recycling or incinerating the
condensed organic layer.  A simplified diagram of a steam stripper is shown
in Figure 4-8.
     Batch steam stripping is used extensively in the laboratory and in
small production units where a single unit may have to serve for many mix-
tures.  Large installations also use batch steam stripping if the material
to be separated contains solids, tars, or resins that may foul or plug a
continuous unit.  Batch steam stripping is also used to treat materials
that are generated from a cyclical or batch process.70  Batch processing
may offer advantages at TSDF because the unit can be operated to optimize
organic removal for a particular type of waste.  For example, the same unit
may be used to remove volatiles from a batch of wastewater, from a waste
containing solids, or from a high-boiling organic matrix.  The heat input
rate and fraction boiled over can be varied for each waste type to obtain
the recovery or removal desired for the specific batch of waste.
     Continuous steam stripping requires a feed stream that is a free-
flowing liquid with a negligible solids content.  Solids, including tars
and resins, tend to foul the column trays or packing and heat exchangers..
Consequently, wastes containing solids may require removal of the solids
prior to processing through a continuous steam stripper.  Unlike the batch
operation, a continuous steam stripper requires a relatively consistent
feed composition to maintain a consistent removal efficiency from the waste
material.71  The continuous steam stripper may offer cost advantages over a
batch operation for applications in which there is little variation in the
type of feed and for relatively high volumes of waste materials.
                                     4-40

-------
                                                  OJ
                                                  3
•a in
I-
§J
Q S
                                                  _OJ
                                                  u
                                                  CD
                                                  QC
ca
I
4^
a
o
Condensed
liquids

t I 1
^^
*ri
c
c
ID
Q ,
u
 ' ^
       e
       a>
       •o
       a
       U
                             E 3.
                             (o a
                             S '=
                                "
                         to
                         S
                         V)

                        i
                            2 o
                                                            cs
                                                            £
                                                         **  a
                                                            I
                                                                       U)
                                                                       z
                                                                       en
                                                                       Q.
                                                                       Q.
52
(A
CO
«<—
o
                                              o
                                              S
                                              OJ

                                             I
                                             CO
                                             >*
                                              OJ
                                                                      u.
              /T
                     2-B S
                     2 S-g
                    I
                    ca
                                     4-41

-------
     The products and residues from steam stripping include the condensed
vapors (condensate),  noncondensible gases, and the treated waste or efflu-
ent.  The condensate usually is decanted to remove any separate organic
layer from the aqueous layer with recycle of the aqueous condensate back to
the feed stream.  The separate organic layer may be recovered and reused as
product or fuel.  If the condensate is a single phase of water containing
dissolved organics, then additional treatment of the condensate may be
necessary for ultimate control of organics.  Most commercial processes rely
on the formation of a separate organic phase and decanting for economical
removal and recovery of organics.  Noncondensibles in the overhead stream
include gases dissolved in the waste material and very volatile compounds
in low concentrations that are not condensed in the overhead system.  The
noncondensibles leave through the condenser or decanter vent and usually
are vented to the atmosphere or to an incinerator.  For example, vinyl
chloride and chloroethane in one steam stripping test were found to pass
through the condenser and were vented as noncondensibles to an inciner-
ator. 72  The effluent from the steam stripper should be essentially free of
the most volatile compounds; however, semivolatiles and compounds that are
relatively nonvolatile may still be present in the stripper bottoms or
effluent and may require additional treatment for removal.
     Steam stripping is applicable to most waste types that have a reason-
ably high vapor-phase concentration of organics at elevated temperatures
(as measured by the vapor/liquid equilibrium coefficient).  These waste
types are commonly found in TSDF.  Theoretically, wastes can be processed
by batch steam stripping if they can be pumped into the unit and if they
produce a residue that can be removed from the still.  This batch operation
may be applicable for waste streams generated in relatively low quantities.
However, batch stripping of sludges with high solids content is not a
technology that has been demonstrated and evaluated in full-scale units.
Consequently, no design or performance data are available for batch strip-
ping of sludges.  Some of the difficulties associated with batch stripping
of sludges include material handling problems, heat transfer in the unit,
long cycle times, and unknown performance.  All of these factors would
affect the basic design and operation of the unit.
                                     4-42

-------
     Preliminary treatment such as solids removal  or pH adjustment are
often used before wastewater is stripped in a continuous unit.   Continuous
steam stripping has been used routinely in the chemical industry to recover
organics for recycle and to pretreat wastewater for organic removal prior
to the conventional wastewater treatment process.   Common steam stripping
applications include recovery of ethylene dichloride, ammonia,  sulfur, or
phenol for recycle and removal of phenol, mercaptans, vinyl chloride,  and
other chlorinated compounds from wastewater.73  Batch steam stripping
appears to be more common at commercial TSDF because it is adaptable to
different types of wastes that may be received in  batches.74  For any given
waste type, pilot-scale evaluations or trials in the full-scale process may
be required to optimize the operating conditions for maximum removal at the
lowest cost.
     Removal efficiencies on the order of 95 to 100 percent are achievable
for volatile organics such as benzene, toluene, and one- or two-carbon
chlorinated compounds.75»76  Batch operations usually provide a single
equilibrium stage of separation, and the removal efficiency is determined
essentially by the equilibrium coefficient and the fraction of the waste
distilled.  The efficiency of a continuous system is related to the
equilibrium coefficient and the number of equilibrium stages, which is
determined primarily by the number of trays or height of packing.  The
organic removal efficiency also is affected by the steam input rate, column
temperatures, and, in some cases, the pH.  Temperature affects the solubil-
ity and partition coefficient of the volatile compound.  The liquid pH also
may affect the solubility and treatability of specific compounds, such as
phenol.  In principle, the removal efficiency in a multistage system can be
designed to achieve almost any level.  In practice, removal efficiencies
are determined by practical limits in the column design (such as maximum
column height or pressure drop) and cost.  Consequently, steam stripping is
difficult to characterize in terms of maximum achievable performance with
respect to percent organic emission reduction or organic concentration in
the treated waste.
     Emission source tests for five steam stripping units are presented in
Appendix F.  Wastewater containing methylene chloride, chloroform, and
                                     4-43

-------
carbon tetrachloride was treated by steam stripping at a chemical plant
(Section F.2.3.1.1).  An inlet concentration of approximately 6,000 ppm
organics was reduced to less than 0.037 ppm for an overall removal effi-
ciency of about 99.999 percent.  The effluent from the stripper required no
further treatment and was discharged directly to a river under a National
Pollutant Discharge Elimination System  (NPDES) permit.
     The steam stripper at a second plant (Section F.2.3.1.2) was used to
strip volatile organics from industrial wastewater.  The major component,
1,2-dichloroethane, was removed from the wastewater at an efficiency of
99.998 percent.  The removal of total organics, which generally included
chlorinated compounds with one to two carbon atoms, averaged 99.8 percent.
     The test at a third chemical manufacturing plant (Section F.2.3.1.3)
evaluated the removal of nitrobenzene and nitrotoluene from wastewater.
These compounds are less volatile than the compounds in the wastewater at
the first plant.  The removal efficiency for nitrobenzene and 2-nitrotolu-
ene ranged from 91 to 97 percent with an overall organics removal of
92 percent.
     The steam stripper at a fourth chemicals manufacturing plant (Section
F.2.3.1.5) is used to remove relatively volatile compounds (methylene
chloride, chloroform, and carbon tetrachloride) from wastewater.  The
removal of the major component, methylene chloride, was 99.99 percent.  The
removal of total organics was 98 percent.
     Four batches of waste were evaluated in a batch steam stripping proc-
ess used to reclaim organic solvents (Section F.2.3.1.4).  The types of
compounds present in the waste included both very volatile compounds and
some considered to be semivolatiles because of their solubility in water.
The removal of the most volatile compounds was on the order of 99 percent.
with occasionally lower values for specific compo.unds (e.g.,  91 percent for
acetone, 87 to 94 percent for 1,1,1-trichloroethane, and 74 percent for
ethyl benzene).  The removal of total organics from the batches ranged from
94 to 99.8 percent.
     At a solvent recycling plant (Section F.2.3.4.1), tests were conducted
on two batches of waste processed through a batch steam distillation unit.
In the first batch, removal of individual compounds ranged from 36 to
                                     4-44

-------
92 percent and total organics removal was 76 percent.   In the second batch,
removal of individual compounds ranged from 12 to 91 percent and total
organics removal was 91 percent.  In this latter batch,  a major portion of
the total organic content of the waste consisted of the most volatile
compound.
     The steam required for steam stripping most likely is supplied by  an
on-site industrial boiler.  Increasing process steam production will
increase boiler air emission impacts.
4.4.2  Air Stripping
     Air stripping is a process that uses forced air to remove volatile
compounds from a less volatile liquid.  The contact between air and liquid
can be accomplished in spray towers, mechanical or diffused-air aeration
systems, and packed towers.77  Packed tower air strippers are preferred for
TSDF organic air emission control because the vapor-laden air can be sent
to a control device, whereas the other devices rely upon dilution in ambi-
ent air to avoid environmental problems.  In packed towers, the liquid  to
be treated is sprayed into the top of a packed column and flows down the
column by gravity.  Air is injected at the bottom of the column and rises
countercurrent to the liquid flow.  The air becomes progressively richer in
organics as it rises through the column and is sent to a control device to
remove or destroy organics in the air stream.  See Figure 4-9 for a sche-
matic of a typical air stripping system with gas-phase organic emission
control.
     The principle of operation is the equilibrium differential between the
concentration of the organics in the waste and the air with which it is in
contact.  Consequently, compounds that are very volatile are the most
easily stripped.  The packing in the column promotes contact between the
air and liquid and enhances the mass transfer of organics to the air.  The
residues from air stripping include the organics-laden air that must be
treated and the water effluent from the air stripper.  This effluent will
contain very low levels of the most volatile organic compounds; however,
semi volatile compounds that are not easily air stripped may still be
present and may require some form of additional treatment before final
disposal.  The process does not offer a significant potential for recovery
                                     4-45

-------
0
0.
§
03
6)
o
8.
a.
        •a
         «
         09
                                       JJ
                                       «^
                                       «••
                                       LU
                                                sr
                                                O)

                                                'a
                                                a.
                            ca
                            >4-
                            o


                            (O
                            CD


                            I

                            en
                            3

                            iZ
         a>.
                        (O
                   Is»
                   C/}    o)
                2
                          4-46

-------
and reuse of organics.  Condensers generally are not used to recover the
stripped organics because of the large energy requirements to cool the
large quantity of noncondensibles (primarily air) and to condense the
relatively low vapor-phase quantities of organic compounds.  Thermal and
catalytic incinerators and carbon adsorption units are the most common
control devices used for control of the overhead gas stream from air
strippers.  Fixed-bed carbon adsorption systems offer some potential for
recovery of organics; however, the decision on type of control (organic
destruction or recovery) is usually based on economics.
     Air stripping has been used primarily on dilute aqueous waste streams
with organic concentrations that range from a few parts per billion to
hundreds of parts per million.  The feed stream should be relatively free
of solids to avoid fouling in the column; consequently, some form of solids
removal may be required for certain aqueous hazardous wastes.  In addition,
dissolved metals that may be oxidized to an insoluble form should be
removed.  Equipment may be designed and operated to air-strip organics from
sludges and solids in a batch operation; however, this application has not
been demonstrated extensively and is not a common practice.  The major
industrial application of air stripping has been in the removal of ammonia
from wastewater.78  in recent years, the use of air strippers has become a
widely used technology in the removal of volatile compounds from contami-
nated groundwater.79,80
     Packed towers can achieve up to 99.9 percent removal of volatiles from
water.81  The major factors affecting removal efficiency include the equi-
librium between the organics and the vapor phase (usually measured by
Henry's law constant for dilute aqueous wastes) and the system's design,
which determines mass transfer rates.  Removal efficiency increases as the
equilibrium coefficient increases; consequently, the extent of removal is
strongly affected by the type of waste and the volatility of the individual
organic constituents.  Mass transfer rates (and removal efficiency) are
also a function of the airrwater ratio, height of packing, and type of
packing.82  The operating temperature is also an important variable that
affects efficiency because of its direct effect on the vapor/liquid
equilibrium.  Higher temperatures result in higher vapor-phase
                                     4-47

-------
concentrations of organics and higher removal rates.  Air strippers have
operational difficulties in freezing weather that may require heating the
input waste stream, heating and insulating the column, or housing the
operation inside an enclosure.  Air strippers are typically designed to
remove key or major constituents.  Compounds more volatile than the design
constituent are removed at or above the design efficiency, and less vola-
tile compounds are removed at a lower efficiency.  Numerous vendors are
available for the design and installation of air strippers.  As is the case
with steam strippers, these vendors usually require pilot-scale tests on
the actual waste material to design the column and to guarantee minimum
removal efficiencies.
     Emission sources associated with an air stripping operation include
tank vents (storage or feed tanks, preliminary treatment tanks) and equip-
ment used to transfer and handle the waste (pumps, valves, etc).  The air
leaving the stripping column usually is treated by incineration (with
destruction efficiencies of 98 percent or higher) or carbon adsorption
(with removal efficiencies of 95 percent or higher if carbon breakthrough
is monitored).  The choice between incineration and carbon adsorption
depends on the specific conditions at the facility.  For example, high
relative humidity in the air stream leaving the air stripper may adversely
affect the adsorption capacity of a carbon bed.  This could be avoided by
choosing incineration.  However, if the air stream contains chlorinated
organics, the incinerated air stream may need to be scrubbed to remove HC1,
leading to higher costs.  In this case, it might be better to choose carbon
adsorption and design to avoid the humidity problem.
     The effluent from the air stripper may be an emission source for
semivolatiles that are not removed efficiently, especially if subsequent
processing includes placement in an evaporation pond or disposal impound-
ment.  Air stripping could be used to reduce organics from wastewater prior
to a wastewater treatment operation.
     An air stripper was evaluated at a Superfund site (Section F.2.3.2.1)
where it is used to remove organics from the leachate collected at the
site.  The evaluation focused on optimizing the removal efficiency for
organic components that represented a relatively wide range in volatility.
                                     4-48

-------
During one test, the removal of the most volatile constituents (1,2,3-
trichloropropane and xylene) ranged from 88 to 98 percent.  The removal  of
semivolatiles such as aniline, phenol, methyl phenol,  and ethyl benzene
ranged from 53 to 70 percent.  The removal of total organics averaged
99 percent.
     Any air emissions, wastewater effluents, or solid wastes associated
with the use of air stripping at TSDF are determined by the type of add-on
control device used in conjunction with the air stripping unit.  Section
4.3 discusses add-on control device cross-media and secondary impacts.
4.4.3  Thin-Film Evaporation
     Thin-film evaporators (TFE) are designed to promote heat transfer by
spreading a thin-layer film of liquid on one side of a metallic surface
while supplying heat to the other side.83  The unique feature of this
equipment is the mechanical agitator device, which permits the processing
of high-viscosity liquids and liquids with suspended solids.  However, if
solid particles are large, a coarse filtration operation may be required to
pretreat the waste stream going to the TFE.  The mechanical agitator pro-
motes the transfer of heat to the material by exposing a large surface area
for the evaporation of volatile compounds and agitates the film to maintain
the solids in suspension without fouling the heat transfer area.  Heat can
be supplied by either steam or hot oil; hot oils are used to heat the mate-
rial to temperatures higher than can be achieved with saturated steam
(>100 °C).  TFE can be operated at atmospheric pressure or under vacuum as
needed based on the characteristics of the material treated.  A TFE is
illustrated in Figure 4-10.
     The two types of mechanically agitated TFE are horizontal and
vertical.  A typical unit consists of a motor-driven rotor with longi-
tudinal blades that rotate concentrically within a heated cylinder.  The
rotating blade has a typical tip speed of 9 to 12 m/s and a clearance of
0.8 to 2.5 mm to the outer shell.  In a vertical design, feed material
enters the feed nozzle above the heated zone and is transported mechan-
ically by the rotor and grating down a helical path on the inner heat
transfer surface while the volatile compounds are volatilized and leave the
evaporator on the top.  The vapor-phase products from TFE are condensed in
a condenser, and the bottom residues are collected for disposal.
                                     4-49

-------
                                       .2
                                       u
           a 3
                      •o
                      CO
                                       
-------
     TFE have been used widely for many years in a number of applications
such as processing of chemicals,  Pharmaceuticals, plastics, and foods.84
Because of their unique features, their use in chemical and waste material
processing has expanded rapidly.   The flexibility in operating temperature
and pressure add potential to TFE for recovering low-boiling-point organics
from a complex waste matrix.
     Although TFE can be used to remove varying levels of organics from a
waste stream, when applied to hazardous petroleum refinery sludges, the
most suitable mode of operation is to evaporate the water and volatiles and
leave most of the hydrocarbons that are less volatile than water.
     With this mode of operation, the TFE bottom residue contains only low
concentrations of both volatile and semivolatile organic compounds and thus
has a low potential for air emissions after ultimate disposal.  This mode
of operation was used during a pilot-scale test discussed below.  Waste
forms suitable for TFE treatment include organic liquids, organic sludge/
slurry, two-phase aqueous/organic liquids, and aqueous sludges.  TFE would
not be used as a means of treating dilute aqueous waste because of the high
water content in the waste.
     Although TFE technology is readily available, as with other organic
removal techniques, a pilot-plant study is usually conducted before full-
scale operation to determine the suitability of the TFE for pretreating a
particular waste stream and to identify optimal operating conditions.  The
EPA recently sponsored a pilot-scale test to assess the performance of a
TFE in removing organics from the different types of petroleum refining
wastes.85  jn that study, 98.4 to 99.99 percent of the volatile and 10 to
75 percent of the semivolatile compounds were removed from the sludge.
These results suggest that a TFE can be used to reduce organics substan-
tially in refinery sludges that are currently land treated.  No commercial -
scale TFE installations have been identified that process the types of
wastes normally handled by TSDF.   However, two installations of TFE used to
recover organics from waste streams have been documented in the literature
and may have some relevance for TSDF operations.86  In one installation
(Section F.2.3.3.3), a hazardous waste recycling plant operates a TFE under
vacuum to separate approximately 95 percent of a feed stream that consists
                                     4-51

-------
of waste oils, a small amount of solids, and approximately 5 percent
organics.  In that operation, toluene is removed from the oily wastes at
less than 85 percent efficiency while both chloroform and methylene
chloride are removed at greater than 99 percent efficiency.  However, that
installation reportedly has significant organic air emissions through the
vacuum pump vent although no estimate was given for the magnitude of the
emissions.  At another organic solvent reclamation and recycling plant
(Section F.2.3.3.2), a TFE operating at atmospheric pressure was able to
remove approximately 76 percent of the acetone and 30 percent of the xylene
from a contaminated acetone waste.  Air samples from the process vent at
that operation indicated that air emissions were negligible.  At a solvent
recycling plant (Section F.2.3.3.1), a TFE showed removal efficiencies of
45 to 99 percent for individual volatile and semivolatile compounds and
yielded a total organic removal efficiency of 74 percent.
     Factors likely to affect or limit the applicability or removal effi-
ciency of TFE include:
     •    Large changes in the properties of the waste being treated,
          which, could cause fouling of the TFE unit.
     •    The requirement for separation of water and condensed organ-
          ics when water is evaporated from the waste stream, which
          adds to the operating expense of the unit.
     The steam required for thin film evaporation most likely is supplied
by an on-site industrial boiler.  Increasing process steam production will
increase boiler air emission impacts.
4.4.4  Batch Distillation
     Batch distillation is a commonly used process for recovery of organics
from wastes.  Its principal use is for recovery of valuable organic chemi-
cals for recycling or reuse and the re-refining of waste oil as discussed
later in this section.  Examples of its use show that it can be applied to
wastes and reduce the organic air emission potential of those wastes by
separating the volatile compounds from the wastes.  Although it has been
applied to aqueous wastes, it has been more typically applied to predomi-
nantly organic wastes.
                                     4-52

-------
     The simplest form of distillation is a batch operation that consists
of a heated vessel (called the pot), a condenser, and one or more receiving
tanks.  This process is identical in principle to batch steam stripping
except that the waste charge is heated indirectly instead of by direct
steam injection.  The waste material is charged to the pot and heated to
boiling; vapors enriched in organics are removed, condensed, and collected
in receiving tanks.  The distillation is continued to a cutoff point deter-
mined by the concentration of organics in the condensate or the concentra-
tion of organics remaining in the batch.  A common modification is to add a
rectifying column and some means of returning a portion of the distillate
as reflux (see Figure 4-11).  Rectification enables the operator to obtain
products from the condensate that have a narrow composition range.  Differ-
ent distillate cuts are made by switching to alternate receivers, at which
time the operating conditions may be changed.  If the distillate is
collected as one product, the distillation is stopped when the combined
distillate reaches the desired average composition.87  Several references
are available that discuss the design and operation of batch distillation
units.88-94  -[^e batch still is operated at a temperature determined by the
boiling point of the waste, which may increase with the time of .operation.
The distillation can be carried out under pressure or under vacuum.  The
use of vacuum reduces the operating temperature and may improve product
recovery, especially when decomposition or chemical reaction occurs at
higher temperatures.
     Batch distillation provides a means for removing organics from a waste
matrix and recovery of the organics by condensation for recycle, sale as
product, or for fuel.  The products and residues include the condensate
that is enriched in organics and recovered, noncondensibles that escape
through the condenser vent, and the waste residue that remains in the pot.
The noncondensibles are composed of gases dissolved in the waste and very
volatile organic compounds with relatively low-vapor phase concentrations.
The waste material after distillation may have been concentrated with high-
boiling-point organics or solids that are not removed with the overhead
vapors.  These still bottoms may be a free-flowing liquid, a viscous
slurry, or an organic material that may solidify upon cooling.  If the
                                     4-53

-------
              i
              e»


             '+5
              CO


              O
             'S
              o
              ia
              O
             1
             J2
              u

             'to
              u
             CO

4-54

-------
waste material contains water, a separate aqueous phase may be generated
with the condensate.  This phase may be returned to the batch or processed
with additional treatment to remove organics or other contaminants.
     Batch distillation may be used for wastes that have a significant
vapor-phase concentration of organics at the distillation temperature.  If
the waste can be pumped and charged to the still pot and the residue can be
removed from the pot, then the waste is likely to be treatable for organic
removal by this process.  Such wastes include dilute aqueous wastes (the
operation would be similar to batch steam stripping), aqueous or organic
sludges, or wastes with volatiles in a high-boiling-point organic solvent
or oil.  The batch distillation of sludges has not been demonstrated and
evaluated in full-scale units; consequently, the processing of sludges in a
batch di'stillation unit is subject to the same limitations described for
the batch steam stripping of sludges (Section 4.4.1).  Batch distillation
has been used to remove organics from plating wastes, phenol from aqueous
wastes, recovery and separation of solvents, and re-refining of waste
oils.95,96  Tne applicability of batch distillation for a specific waste
type can be evaluated by a simple laboratory distillation to assess poten-
tial organic recovery.  As with other organic removal techniques, the
process may require optimization in a pilot-scale or full-scale system for
different types of wastes to determine operating conditions that provide
the desired distillate composition or percent removal from the waste.
     Batch stills usually are operated as a single equilibrium stage  (i.e.,
with no reflux); consequently, the organic removal efficiency is primarily
a function of the vapor/liquid equilibrium coefficient of the organics at
distillation temperatures and the fraction of the waste boiled over as
distillate.  The use of a rectifying section yields an overhead product
with a composition that can be controlled by the operator.  The removal
efficiency for various waste types can be highly variable because of the
dependence on both properties of the waste  (e.g., organic equilibrium) and
the operating conditions that are used.  Emission tests were conducted on a
batch unit at a plant engaged in the reclamation of contaminated solvents
and other chemicals.97  The test results (summarized in Appendix F, Section
F.2.3.4.2) indicate organic removal efficiencies on the order of 99.4 to
                                     4-55

-------
99.97 percent for organics, including compounds such as methyl ethyl
ketone, 2,2-dimethyl oxirane, methanol,  methylene chloride, isopropanol,
and carbon tetrachloride.  Results for a second distillation unit at the
same site processing contaminated solvents showed organic removal efficien-
cies ranged from 97 percent (for xylene and ethyl benzene) to 99.9 percent
(for trichloroethane).  These results demonstrate that batch distillation
has been used successfully to remove organics from aqueous and organic
wastes or solvents.
     The steam required for batch distillation most likely is supplied by
an on-site industrial boiler.  Increasing process steam production will
increase boiler air emission impacts.
4.4.5  Dewatering
     As used herein, dewatering refers to solid-liquid separation achieved
by filtration or centrifugation.  Such devices normally are characterized
according to the force used to achieve the desired separation.  At TSDF,
solid-liquid separation most often is achieved by filtration rather than
centrifugation.  Filtration is achieved by passing the waste stream through
a filtering medium, often a textile product, using force that may be
applied in any of several ways.  Press-type filters consist of a series of
plates covered with a filtering medium and enclosed in a frame.  Separation
is achieved by filling the void spaces between plates with the input mater-
ial and then applying pressure to force the plates together and generate
the desired separation.  Examples of this type of filter include plate and
frame, recessed plate, and pressure leaf filters.98  Filtration force also
may be applied by using atmospheric pressure on one side of the filter
medium while the other side is maintained at greater or lesser than atmos-
pheric pressure.  Examples of this type of filter include rotary drum
vacuum and rotary drum pressure filters.  In rotary drum vacuum filters,
the driving force is achieved by reducing the pressure inside a rotating
drum to below atmospheric.  The drum is covered with a filter medium that
builds up a cake of solids that contributes to filtration efficiency.  The
rotary drum pressure filter uses the reverse principle of applying greater
than atmospheric pressure to the inside of the rotating drum.  In these
filters, the filtering medium is inside the drum.  Advantages of the vacuum
                                     4-56

-------
filter include its adaptability to continuous operation and the ease with
which the filter material can be cleaned and maintained.99  In recent
years, belt filter presses have become one of the more widely used types
for many applications.  These filters use a combination of gravity and
pressure to apply force across the filter medium.  In belt filter presses,
the input stream is applied to a horizontal moving belt that is covered
with filter material.  Gravity forces cause partial separation of the
liquid from the solids in the stream.  As the belt continues to move, it
approaches a second moving belt, and the two move along together over a
series of rollers that force the belts closer and closer together, creating
pressure on the material between the two belts.  The belts separate for
solids removal, and the filter medium separates from the underlying sup-
porting web.  At this point, the filter medium can be washed continuously.
The ease of continuous washing is one of the primary advantages of the belt
filter press.100  Other advantages include the adaptability to continuous
operation and the higher throughputs handled relative to other types of
filters.  Exit streams from a filtering or dewatering operation include the
filtrate, which is mostly free of solids, and the filter cake, which gen-
erally has a sufficiently low moisture content to be handled using solids
handling techniques.  A schematic diagram of a dewatering system is illus-
trated in Figure 4-12.
     Dewatering is applicable to any waste stream that consists of a sludge
or slurry such as petroleum refinery sludges.  When used for this applica-
tion, toxic metals remain in the filter cake, which could continue to be
land treated or may be fixated and landfilled, while the liquid passes
through a separation process where oil (which will contain a large fraction
of the organics) is recovered for recycle.  Little data have been identi-
fied that can be used to estimate the emission reduction achieved by
dewatering.  However, Chevron Research Company has conducted tests that
indicate as much as 90 percent of the oil in refinery sludges can be recov-
ered by dewatering and that oil recovery is improved substantially if the
filtration or centrifugation step is followed by a drying step.101  At an
EPA-sponsored test at a Midwest refinery, oil removal using a belt filter
was found to be 78 percent for an API separator sludge and 66 percent for a
                                     4-57

-------
                                        
-------
dissolved air flotation (DAF) float.102  If the recovery efficiencies
obtained in the tests can be achieved in full-scale applications,  an
equivalent reduction in emissions from land treatment or landfill  opera-
tions would be expected.
     Emissions during dewatering would come from pumps,  valves, storage,
and other handling operations and also from any exposed  waste surfaces at
the dewatering device.  At the test of the belt filter press cited above,
measured air emissions were equal to 21 percent of the volatiles in the API
separator sludge and 13 percent of the volatiles and 22  percent of the
semivolatiles in the DAF float.
     When vacuum filters are used, emissions would occur with the vacuum
pump exhaust.  Control of emissions could be achieved by enclosing the
operation where necessary and venting the enclosure to one of the add-on
control devices described in Section 4.3.  Vacuum pump exhaust also could
be controlled with an add-on control device.
     Any air emissions, wastewater effluents,  or solid wastes associated
with the use of dewatering are determined by the type of add-on control
device used in conjunction with the dewatering device.  Add-on control
device cross-media and secondary impacts are discussed in Section 4.2.
4.4.6  Hazardous Haste Incineration
     Incineration is an engineered process that uses thermal oxidation of a
bulk or containerized waste to produce a less bulky, toxic, or noxious
material.  Combustion temperature, residence time, and proper mixing are
crucial in controlling operating conditions.103,104  of the several types
of waste incineration systems, four are generally cited as being the most
useful and having the greatest potential for application to wastes proc-
essed at TSDF.  They are liquid injection, rotary kiln,  fluidized-bed, and
multiple-hearth incinerators.  The type of incinerator selected for a par-
ticular installation depends on the waste type and composition as well as
other factors such as whether the waste is in bulk or containerized.
     Liquid injection incinerators are versatile and can be used to dispose
of virtually any combustible liquid that can be pumped.   The liquid waste
must be converted to gas prior to combustion.  This change is brought about
in the combustion chamber and is generally expedited by increasing the
                                     4-59

-------
waste surface area by atomization.105  Liquid injection incinerators oper-
ate at temperatures between 820 and 1,600 °C.  Gas-phase residence times
range from 0.1 to 2 s.
     Rotary kilns are versatile units that can be used to dispose of
solids, liquids, slurries, and gaseous combustible wastes.  Rotary kilns
are long, cylindrical rotating furnaces lined with firebrick or other
refractory material in which solids are combusted by themselves or are
incinerated by combustion of an auxiliary fuel or liquid wastes.  Combus-
tion temperatures range from 870 to 1,600 °C depending on the waste
material character!sties.106  Solids residence time varies from seconds to
hours, depending on the type of waste.  Unless the kiln is very long (i.e,
provides a larger residence time), some type of secondary burning chamber
usually is required to complete combustion of the solid waste.  The heat
release per unit volume is generally quite low, but the rotary kiln pro-
vides a method of mixing solids with combustion air and can be operated at
temperatures in excess of 1,400 °C that are unavailable in other types of
systems.
     A fluidized-bed incinerator consists of a bed of inert granular mate-
rial fluidized by hot air onto which the waste and auxiliary fuel is
injected.107  yne waste in turn combusts and returns energy to the bed
material; thus, heat release per unit volume is generally higher than for
other types of incinerators.  Fluidized-bed incinerators operate at temper-
atures below the softening point of the bed medium, usually around 450 to
850 °C.108  The residence time is generally around 12 to 14 s for a liquid
waste and longer for solid wastes.  This type of incinerator is suited
particularly to heavy sludge and to certain types of organic/inorganic
mixtures.  The inorganic material will stay in the bed and can be removed
as ash.  Scrubbing of flue gases usually is required to remove fine partic-
ulates, and subsequent flue gas treatment is required for halogen, sulfur,
and phosphorus compounds.
     The multiple-hearth incinerator was designed for the incineration of
low heat content waste such as sewage sludge.  It generally uses large
amounts of auxiliary fuel and is large in size.  A multiple-hearth unit
generally has three operating zones:  the uppermost hearths where feed is
                                     4-60

-------
dried (350 to 550 °C),  the incineration zone (800 to 1,000 °C),  and the
cooling zone (200 to 350 "C).^9  Exit gases have good potential for heat
recovery, being around 300 to 600 °C.  Temperatures on each hearth can be
maintained using supplemental fuel.  Multiple-hearth units may be suitable
for hazardous sludge disposal, although it may be necessary to add an
afterburner to destroy unburned hydrocarbons that volatilize on the upper-
most hearths.  Several  incinerator types are shown in Figure 4-13.
     The cost of operating an incinerator can be reduced by recovering and
using the heat generated by the combustion of waste.  Primary heat recovery
can be employed by using the incinerator exhaust to preheat the incoming
waste stream.  Secondary heat recovery, such as a waste heat boiler, can
also be used if the production process can make use of the steam generated.
Heat recovery is shown in the incinerator illustration in Figure 4-13.
     Incineration under proper control and using proper techniques will
provide total destruction of all forms of hazardous organic wastes.HO
There are two basic types of wastes:   (1) combustible wastes, which will
sustain combustion without auxiliary fuel; and (2) noncombustible wastes,
which usually contain large amounts of water or other inert compounds and
will not sustain combustion without auxiliary fuel.  Organic liquid and
sludge are most suitable for incineration because of their heat content.
Aqueous sludge, two-phase aqueous/sludge, and organic-containing solids may
be incinerated with auxiliary fuel to destruct hazardous organics.  Dilute
aqueous waste would not be suitable for direct incineration because of its
high water content.
     Of the four types of incineration, liquid injection and rotary kiln
have been proven to destruct hazardous waste and to be commercially avail-
able; fluidized-bed and multiple-hearth are less frequently used tech-
nologies.  However, fluidized-bed incinerators may have greater potential
because of their compact design, which results in relatively low capital
cost, and their general applicability to solids, liquids, gases, and wastes
containing inorganics.HI
     Air emission standards of performance for incinerators burning
hazardous waste have been established by EPA.H2  Existing standards
require that each incinerator (i) achieve a destruction and removal
                                     4-61

-------
                                            PROCESS STEAM
                                                     STACK
     MMBUSTOFIsjf
        SOUOS
        FEED
      LIQUID-
      FEED
        &  AIH  •*
        fO
        FAN
       UQUIOWASTT
                  Fluidized-Bed Incinerator
 STORAC!
   WAST*
CONDITIONING
                                           OISKR90N STACK


                                            FRKOOUR
SCRUBBED

  -o
r
IT
                                        UAKturwATtK
                                         WATtRTRCATUENT

                 Liquid Injection Incinerator
            PLENUM AIR
           _ BLOWER
                   Rotary Kiln Incinerator

        Figure 4-13. Hazardous waste incinerators.
                          4-62

-------
efficiency (ORE) of 99.99 percent for each principal  organic hazardous
constituent (POHC) designated for each waste stream;  (2)  have hydrogen
chloride (HC1) emissions not to exceed the larger of 1.8 kg/h (4 Ib/h) or
1 percent of the HC1 in the incinerator exhaust gas upstream of any
emission control device; and (3) have total particulate matter emissions
not to exceed 0.18 grams per dry standard cubic meter (0.08 grains/dscf).
Additional standards are being developed by EPA to improve the control of
toxic metals, HC1, carbon monoxide, and residual organics.
     To meet Federal and State standards, complex air pollution control
systems are installed on hazardous waste incinerators.  These control
systems include the use of wet or dry scrubbers in conjunction with fabric
filter or electrostatic precipitator control devices.  Control system oper-
ation results in the production of solid wastes and,  if a wet scrubber is
used, wastewater effluents.  Additional solid waste is produced by the
incombustible material or ash that is removed from the incinerator and must
be disposed as a hazardous material.
4.5  PROCESS MODIFICATIONS
4.5.1  Petroleum Refinery HasteCoking
     Delayed coking is a process used in some petroleum refineries to
recover useful products from the heavy ends of the raw petroleum.  In this
process, the feed stream enters a fractionator where gas oil, gasoline, and
lighter fractions are flashed off and recovered.  The fractionator bottoms
are combined with a recycle stream and heated to reaction temperatures of
480 to 580 °C in the coker heater.  The vapor-liquid mixture from the
heater then enters the coke drum, where the primary coking reaction takes
place.  The coke drum provides the proper  residence time, pressure, and
temperature for coking.  In the coke drum, the vapor portion of the feed
undergoes further cracking as it passes through the drum, and the liquid
portion undergoes successive cracking and  polymerization until it is con-
verted to vapor and coke.113  Coking units consist of at least two coke
drums so that one can remain online while  coke is removed from the other.
     In removal of coke from the drum, steam is first injected into the
drum to remove hydrocarbon vapors, which are cooled to form a steam-hydro-
carbon mixture.  This is followed by water injection to cool the coke  and
                                     4-63

-------
allow removal.  When the coke is cooled sufficiently, a high-pressure water
jet is used to cut the coke into pieces that are then removed from the coke
drum.
     Coking is an alternative to the land treatment or landfilling of
petroleum refinery hazardous wastes according to the requirements specified
in the Federal Register.H4  coke produced from petroleum refinery hazard-
ous wastes is exempt from regulation as a hazardous waste, if the waste is
coked at the facility where the waste is generated.  In addition, the coke
cannot exhibit any of the characteristics of a hazardous waste.
     Refinery sludges can be introduced to a delayed coking operation in
one of two ways.  In one process, sludge is injected into the coker during
the cool-down period.  In that process, the water content of the sludge
contributes to cooling the coke while organics are cracked into products or
polymerized into coke.  Sludge solids are immobilized inside the coke.^5
This process currently is used at several refineries.  In the second
process, sludge is introduced into the coker as a part of the feed stream
by injecting it into the blowdown system where it is vaporized and recy-
cled.  In that process, the amount of sludge that can be added to the feed
stream must not exceed some small percentage of the total feed, and the
sludge must undergo extensive dewatering prior to entering the coking oper-
ation. H6  Only one refinery is known to use this operation.
     No emission measurement data were found for coking operations; how-
ever, because the entire operation is enclosed, organic air emissions are
estimated to be quite low.  Some emissions would be expected from transfer,
storage, and handling operations associated with coking.  Most of these
would be expected to come from the transportation of sludge from the point
of generation to the coking operation and from storage of sludge at the
coker.  Although no definitive data are available to permit estimates of
the emission reduction that would be achieved by processing refinery
sludges through a coker rather than land treating,  reductions approaching
100 percent are expected.  Increased emissions from the coking operation as
a result of introducing wastes into the feed stream are estimated to be
negligible.
                                     4-64

-------
     Coking is a possible control  option at refineries that produce fuel-
grade coke.  At refineries that produce high-quality,  electrode-grade coke,
the quality degradation caused by sludge injection may be unacceptable.
For refineries that do not have an existing coking operation,  coking would
not be a practical emission control alternative.
     Application of coking for TSDF organic air emission control  essen-
tially involves using refinery sludges as additional feed materials for  an
existing refinery process unit.  Existing petroleum coking units  are oper-
ated to improve overall refinery product yield and economics.   Therefore,
no cross-media or secondary impacts are attributed to the organic air
emission reduction achieved by coking of petroleum refinery wastes.
4.5.2  Submerged Loading
     Organic air emissions generated during TSDF waste loading operations
are the primary source of evaporative emissions from waste containers
(e.g., tank trucks and drums).  Emissions occur when liquid or semi liquid
wastes are poured into a container displacing—from inside the container to
the ambient air--an equal volume of air that is saturated or nearly satu-
rated with organics.  The quantity of organics emitted is a function of the
loading method and whether the container is clean before loading.
     For splash loading, the influent pipe dispensing the waste is lowered
only partially into the container.  Consequently, the waste flows from the
end of the pipe that is above the liquid level in the tank or drum.  Sig-
nificant turbulence and vapor-liquid contact occur when the falling liquid
splashes on the surface of the liquid already in the container.  This
results in organic vapor generation and emission to the atmosphere through
the container opening used for waste loading.  Control of loading air emis-
sions can be accomplished by using submerged loading.  During submerged
loading, the influent pipe opening is located below the liquid surface
level.  This position decreases turbulence and evaporation, and eliminates
liquid entrainment.
     The quantity of organic air emissions is also affected by the condi-
tion of the container prior to loading.  If a clean container is used, only
the vapors generated by the loading operation are emitted.  However, if the
container contains residue vapors from a previous waste!oad, then addi-
tional emissions will be released when the container is filled.
                                    4-65

-------
     No emission source test studies of TSDF container loading have been
conducted.  To estimate the effectiveness of submerged loading in suppres-
sing organic air emissions, an emission model derived for estimating emis-
sions from loading petroleum liquids into trucks, tank cars, and marine
vessels was used.  A complete description of the emission model, as well as
the analysis, are presented in Appendix H, Section H.I.3.  Use of submerged
loading is estimated to reduce organic air emissions from TSDF waste load-
ing operations by 65 percent.
     Submerged loading of open area sources, such as surface impoundments
or open-top tanks, is not considered a control technique unless it is used
in conjunction with covers or enclosures over the source.  If the loading
is changed from above to below the liquid surface in the absence of covers
or enclosures, organics that would have been emitted during filling are
instead emitted quickly from the open liquid surface by wind blowing across
the source.  However, if the open-top tank is covered or if the impoundment
is enclosed, then emissions may be generated from the displacement of vapor
by liquid.  In this case, submerged loading may reduce emissions as
described above for containers, and would provide additional control of
organic air emissions.
     There are no cross-media or secondary environmental impacts associated
with submerged loading.
4.5.3  Subsurface Injection
     Subsurface injection is a land treatment practice in which waste is
injected directly into the soil.  The process could be used to apply wastes
to a land treatment site in lieu of surface application.  In subsurface
injection, as opposed to surface application, there is no pooling of liquid
on the soil surface and thus potentially less opportunity for the material
to be emitted to the atmosphere.  However, in a field study to evaluate the
relative air emissions from land treatment plots using surface application
and subsurface injection, no difference in emissions was evident.117
Therefore, subsurface injection is not currently being considered for air
emission control.
4.5.4  Haste Fixation Mechanical Mixing
     As a result of the RCRA land disposal restrictions, many liquid,
slurry, and sludge types of hazardous wastes are now treated at TSDF using
                                    4-66

-------
a waste fixation process so that the waste can be disposed in a hazardous
waste landfill.  Waste fixation, also referred to as waste solidification
or stabilization, is a chemical process in which the free water in the
waste reacts with a binder (i.e., cement) to form a solid material that
immobilizes specific metal and organic contaminants in the waste for which
treatment standards have been set.
     Waste fixation involves first mixing the waste with the binder
material.  The binder can be either an inorganic or organic material.  The
prevalent TSDF industry practice is to use the least expensive binder
material locally available (usually cement kiln or lime kiln dust).  Typi-
cally, the waste and binder are mixed together in proportions to produce a
moist, soil-like material.  Following mixing, the mixture is cured by hold-
ing the mixture for a sufficient period of time (usually 24 to 48 h to
allow the mixture to harden.  The waste is then tested, and if it meets the
appropriate treatment standards, the waste is transferred to a landfill.
More information about TSDF waste fixation practices is presented in Refer-
ences .118 and 119.
     Organic emissions from waste fixation occur when organics in the waste
volatilize and are released to the atmosphere during mixing and curing.
Results from a laboratory study of waste fixation suggest that the majority
of organic emissions occur during the mixing of the waste and the
binder.120  por this study, organic emissions were measured for bench-scale
simulations of waste fixation processes.  Approximately 60 to 90 percent of
the volatile organics in the waste were emitted during mixing of the waste
and binder.  The percentage varied depending on the type of binder used.
The bulk of the remainder of the volatile organics was emitted during the
curing step.
     The simplest mixing procedure used at TSDF involves placing the waste
into an open-pit or open-top tank, dumping the binder into the waste, and
mixing the materials using heavy construction equipment such as a backhoe.
A similar procedure is used, but on a smaller scale, for fixating waste
directly in a drum.  For this operation, a worker manually adds the fixa-
tive into the open-top drum containing the waste and mixes the materials
with a small auger or blender.  At some TSDF, open mixing of the waste and
                                    4-67

-------
fixative has been replaced by enclosed mechanical mixing devices such as a
pug mill and a ribbon blender.
     Observation of waste fixation operations at sites throughout the
United States indicates that mechanical mixers effectively control air
emissions from the mixing of the waste and binder.121-126  jne mixer
enclosure can be vented directly to an add-on control device.  Controlling
organic emissions is demonstrated by the use of carbon adsorption systems
in combination with particulate controls on pug mills at two waste fixation
facilities.127,128  These controls have been installed to meet State or
local air emission regulations.
4.6  WORK PRACTICE MODIFICATION
4.6.1  Housekeeping in Drum Storage Areas
     Drum storage is the temporary holding of liquid, semi sol id, or solid
wastes until treatment and/or disposal can be undertaken.  Drums can be
stored on concrete pads that have a perimeter curb and gutter for secondary
containment.  Secondary containment is required at any drum storage area
(40 CFR 264.175), and spilled or leaked waste and accumulated precipitation
must be removed from the sump or collection area in as timely a manner as
necessary to prevent overflow of the collection system.
     Typically, drums are sealed and in good condition during storage;
therefore, the potential for breathing emissions is assumed to be negligi-
ble.  However, drums may rupture and leak hazardous wastes during storage
or transfer.  Management and technical practices not only cause spillage,
they also determine what fraction is available for volatilization.  Because
RCRA requires that container storage areas be inspected weekly for con-
tainer leaks and deterioration (40 CFR 264.174), a 50-percent loss of the
volatiles to the atmosphere from the spilled waste was selected for emis-
sion estimating purposes; the remaining 50 percent are recovered as a
result of implementing RCRA spill response actions.
     Two control options are considered appropriate for reducing emissions
from drum storage:  one option is to vent the existing enclosed drum stor-
age areas through a fixed-bed carbon adsorption system (see Section 4.2.2
for more detail).  The other control option is to use an open secondary
containment area, conduct daily inspections and maintenance, and have a
                                    4-68

-------
policy to clean up spills within 24 hours of discovery.  This option is an
adaptation of the proposed 1986 RCRA tank regulations  (40 CFR 264.196).
Leak detection of stored drums is accomplished by visual inspection on a
daily basis.  In case of a spill or leak, sorbent material is used to clean
.up the spillage, or the spillage is collected in a collection sump for
transfer to a drum for treatment or disposal.  This policy of daily inspec-
tion with cleanup within 24 hours decreases the fraction of volatiles lost
to the atmosphere.  The magnitude,of the reduction will depend on operating
practices, waste type, and volatiles concentration; however, no data are
available that quantify the emission reduction achieved by this method.
Because it is estimated that these housekeeping practices are already used
at most TSDF, no credit for an emission reduction was  included in the
estimates of nationwide emissions.
4.6.2  Leak Detection and Repair
     Waste transfer operations often involve pumping waste through pipe-
lines into a variety of waste management process units.  This pumping
creates the potential for equipment leak (fugitive) emissions from pump
seals, valves, pressure-relief valves, sampling connections, and open-ended
lines and flanges.  Leaks from these types of equipment are generally ran-
dom occurrences that are independent of temperature, pressure, and other
process variables.  However, these leaks do show a correlation with the
vapor pressure of the material in the  line.  For example, monthly inspec-
tion data from the synthetic organic chemicals manufacturing industries
(SOCMI) show that 8.8 percent of the seals on pumps handling light liquids
have leaks and only 2.1 percent of the seals on pumps  handling heavy
liquids have leaks.129  Light liquids  are defined as those containing at
least 20 percent by weight of organic  compounds having a vapor pressure
greater than 10 mm Hg.                           ,     -
     An effective method for controlling fugitive emissions is to implement
a  routine leak detection and repair program  (i.e., periodic inspection and
maintenance).  Leaks can be detected by  individual component surveys, which
may be carried out independently or may  be a part of activities such as
area  (walkthrough) surveys, fixed-point monitoring, and visual inspection.
Leaks can be repaired by adjusting the tightness of parts  in pumps, valves,
                                     4-69

-------
pressure-relief valves, closed-loop sampling, and capping or plugging open-
ended lines or by replacing faulty devices.  The use of portable organic
vapor detection instruments during individual component surveys is consid-
ered to be the best method for identifying leaks of organics from valves
and pump seals;130 use Of such instruments constitutes the only type of
leak detection method for which a control efficiency has been quantified.
     The control efficiency of individual component surveys depends on:
(1) action level or leak definition,  (2) monitoring interval or frequency,
(3) achievable emission reduction of maintenance, and (4) interval between
detection and repair of the leak.  Background information developed by EPA
to support standards for SOCMI fugitive emissions indicates that a monthly
inspection and repair program of systems handling light liquid reduces
fugitive emissions from pumps by 61 percent and from valves by 46 per-
cent. 131  The study also shows that closed-loop sampling and capping open-
ended lines provide 100 percent control of these emission sources.  Consid-
ering the similarity between SOCMI sources and TSDF sources, these prac-
tices are expected to give equivalent reductions at TSDF.  Nationwide
emission reductions were estimated based on the above emission reductions
along with the estimated relative numbers of pumps, valves, sampling con-
nections, and open-ended lines in the waste management system.  Combined,
these control techniques provide weighted control efficiencies of 70 per-
cent for systems handling light liquids and 78 percent for systems handling
heavy liquids.
4.7   SUMMARY OF CONTROL TECHNOLOGIES SELECTED FOR CONTROL OPTION
      ANALYSES
     A control option is a combination of control technologies applied to
TSDF emission source categories to reduce nationwide TSDF organic air emis-
sions.  The selection of control options and estimates of the nationwide
organic air emission, health risk, environmental, and cost impacts of
options are discussed beginning in Chapter 5.0.
     Table 4-2 lists the types of control technologies that are selected in
Chapter 5.0 for reducing organic air emissions from each TSDF emission
source category.  Table 4-3 shows the emission reduction efficiencies used
in the nationwide impacts analysis for specific control options applied to
specific emission sources.
                                    4-70

-------
            TABLE 4-2.  EMISSION CONTROL OPTIONS USED FOR SELECTING
                             TSDF CONTROL OPTIONS9
    Management process
     source category
                                                 Control options*3
Suppression  .Add-on
            Process
       modification/work
           practices
Quiescent surface impoundment0
  Storage or treatment

  Disposal
Dumpster storage

Quiescent (storage or treatment) tank
  Uncovered
  Covered

Waste fixation
  Pit

  Enclosed mechanical mixer

Aerated/agitated surface impoundment
  (treatment)

Aerated/agitated uncovered tank
  (treatment)

Land treatment
    X
    X
    No direct controls; pretreat to
    remove organics or incinerate wastes"
    X
    X
X

X


X

X

X
    No direct controls; pretreat to
    remove organics, incinerate, or
    coke wastes6
Active landfill
Closed landfill
Wastepile
Equipment leaks
Pumps, valves, and
pressure-relief valves
X
X
X




X
(continued)
                                    4-71

-------
                              TABLE 4-2 (continued)
                                                 Control options^3
    Management process
     source category
Suppression   Add-on
     Process
modification/work
    practices
Equipment leaks (con.)
  Sampling connections

  Open-ended lines

Drum storage with enclosure^

Drum and tank truck loading

Spills

Organic compound removal devices

All TSDF process/emission sources
                               X

                               X
                X

                X
TSDF = Transfer, storage, and disposal facilities.

HW   = Hazardous waste.

aThe development of control strategies is discussed in Chapter 5.0.

^Emission control options are of four types; examples of each control type
 are given in Table 4-1.  Specific control options evaluated in this study
 are identified in Table 4-3.

clncludes treatment impoundments that are dredged annually and that are thus
 exempt from land disposal restriction regulations.

"Disposal surface impoundments function via evaporation.  Direct controls
 such as covers inhibit evaporation.

eCoking is a control option only at refineries that have an existing coking
 operation and that meet the conditions specified in a November 1985 Federal
 Register notice.132

fbrums and containers are stored in a building that can be vented to a
 control device.
                                    4-72

-------








<2
t-
a
^

I
U.
o
e
i
UJ
1


i
z
H
P
z
n
9
4 CONTROL EFFICIEN
S
i
i
a
m


"o
L.
x 1

j _
*• "•
i i
oe
u
i j
° s
c e
0 1.
&
•a a.
U 3
a in
s 0
4
J

1
O

s
i



8
Control devi




nagement procea
ource category
5-


i i
i i



i i




to to
CO «



ii





< <




brane
e vented
adaorber*
king aynthetic mam
•upported atructur
fixed-bed carbon
e i o
— i •**

j
C
5
*^
e o
X U
""






0>



!


M
3
t

ro

S





<

a
5
_•
e e
• u
]l
b. e
• o
J roof v«nt«d to c
•xlating combust!
j «
UL






!



1
1


s
a»
a
i
CO
3

f-4





<




TJ
|
i roof vented to f
rbon adaorberfl
e m
x u
uT






i to i
1 0> 1



: i :



2
+ : §
N.


. . §
i i s



h.

"*- 3 <


c e
O .A
O 4> •»
te e
3 x
= 1 =
0 U 0
•*> 4*
*•* a
•s ~s ^ i
£1I s
i:* :
•4» C U C
* •» o •
- * a **
**•*»• t. ••-
- S 5 . §
• b • U 1.
C 1 — — 1
• "•••*•
a — ° "° —
11 u. u.


•s
I.
•
J


ID 1O



1 1
1 1




1 1
1 1



§ i





< <



•••> -••
U U
"c "c
111
•bon adaorberfl
lion with encloaed
ier with control d
lion with encloaed
5 515
H iZ

s
Ixatlon
•ed mechanical i
«- 0
Jii 1
• o. ui


!•



!




IO
a



i





<



o
1^
8?i
S . fe
(er with control d
lupported atructun
ted-bed carbon ada<
1 u *
<

8 ?
/agitated aurfai
udment (treatmei
•W "3
\ 1
\~


1 1 1
1 --till



1 1 1 1 1
1 1 t 1 1



r*» n
Si ea • •
a a
a -*r


Q fill
-i-t i i i i



**•
— « •
— N t-*) • to




•s
J3
T>
 • e
^ L. "™
•!-?*•?
e • -o 5
i - S .2
< _J w
^
3
C
1
S""


























_a
0
1
4>
(O
4-73

-------






























1
1
„«
„
^
UJ
<
*~




















—
4>
e
K 0
U



I _
ji
c
a o

0 "•
c S
o u
4> IX
U 3
£ w


UJ
u
L.
3
4*
£
^
U
O
**
5
*
£






U

1
O
t.
c
o
u








m
M
• X
u i?
o o
u o
a. •
4>
49 •
i °
is
?=•
c o
3"

i i t i i i i
i i i i i i i






i i i i i i i
i i i i i i i




O . • 9} • • B
o> » o> at fi
at m o> T







i i i i i i i
i i i i i i i
2 2
3 3
*• f* ^O* T
f* « ID* V* • IO* — —
"• -r N w
•& 2
3l






L
a.
s
• i 1
s s
uj ° £
E; UJ -a
1 i I
•H PI _J







II
C —
o -o

49 •
U l
I J? 8 =
O • >
U ^ —
ex >
.2 ^ -g *
1 ill
• tO 3 Q. 0.
S uT

1
1






1
I




CD








1
















a
c
|
• •
o»
0. 3
J »
t t_
•o o
o
• *
o a.
— •








c
j>

4> N
S J
C —
o
U t)
o-S
e c
— *
H
CO O

ID 1 1
O 1 1






1 1 1
1 1 1




1 ID »
1 «D 10







t 1 1
1 1 1



1 — —
1 < <











01
11-
0 — jf
^ TJ "a
O) •
Us
J 5 5




~s ?
3 —
S "S
— 0

c
• Jf
u
1 1
a •
m 4>
L.
o *e
49 C
E e —
33 —
o o to
JC
S
SCO O» O 1O
O> 1 CB 0»






1 1 I 1 1
t 1 I 1 1




1 1 1 1 1
1 1 1 1 1







1 1 1 I 1
1 1 1 1 1



1 t 1 1 1
I 1 1 1 1








~i
u
— • L.
> O
-s • |
El Sfe
4> O C J)
e c — L
«;fcjj
llJli
— 4> e • u
x • o ^ •
UJ U U K U


•
>
-S

~





1
o
1
u
e
•
01
o








































*
—
u
«*>
s
Q.

*?
X C

c -



o » —

4> II > •
•5 ..^
SU 3 —
• 00.
-D«^TI o.
1 M U *
4T C •
01 • N 4>
= £££
ii u u it
1" '
5l?
*> > 3
-£§II
49 i. C e
e •*- o
o t. u
U II O *-*
u
c— •
o c u
_ • —
« • o
Ml
4> Ql
X C

.1 E ?
•^ii
• II
:?•§
o. u
1. X

c o
c
• • 0
I5:
'-o
C • 4>
"• £ o
4» S
e^
o« x

>2.*^
15*
^ ^ S
5 • 5
• u
eao
S"S °-
„•"• S

• L. O
**» CD «
O C •
?K
J||
• ° •»
CXI-
°*s
m N c
* C V
"i-2 g
4>— 5 E
• • "« 5
«•- u
«*-•)« 4>
* n£ "

X U 49
• a« e
E a. t. •
3 0 >
8 *"£ •
O 49 •
1. •- 01 U
4> • •—
8SS?

-------






























^N
I
4>
g
U

m
t


UJ
S






























i

3
£
c

3
C

—
•»
8
L.

O
*
g
i

1

o

jj
c
g
V
^
0
J
J>
u

o.
•
si

..Sf. £• ?l
|?J - I | !
5 — "a" n-o^" S «
— • ra 3— CB • 3 c
•*. 49 -O o 9*9 3 O1 —
— C3eO*3Oef U
49 O— 3 — — e C
gy"r-"S8.2
•v u » u u— e u
Em 9 9 • • o i •*-
ca 3— one e e
o u o-— ^iS.* -
49 *X CI ffi  *>» 49
n &
0? V*






e
0
49
I
L.
e
o




u
S
^
dispose

1-
e

E
O
u
•**




3
5
L.
tl


•**
I
X
^
C
c
1
1
•o
s


JZ
^

nt Itnpoundmon
|
49
|












































49
e

1
3
O
1
e
49

1 Is returned
*Desorbed materta














































g

™
49
•
S

3
1
U
X
•Efficiencies var
5
M
*
1
4>
O
•
_o

«
£
U
m
JC
U


*c
49
g
C
1
Q.
-S

J

t.
>

C
49

C

C
S

49


»
j

*
1
O
C
•
N
U
CeV

«
e

c
49

|
t
^
e
•*»
•
•».
o
X
u
c
e
*w
•*.
•5
e
,.
5-
,-•_•
_u— *>
I'**


O 1. C
^ o*;
o o »
:ii
o a.
4>^ •



4» •
e 4> e
e = —
• y
^ u
O«D 3
ooi-c
-^s--
SoJ

•». •

•C O C
«•••»•••
H« O •
49
e o
. Q4»

e 49 •

• ?49
4T

•
5||


lii
u*>
E E1>
- * E
• e L
|i|
s*~
• E —
e e e
L U —
JSii
E 3 O.49

J* S
e e -D
i.
*- C"V O
o e e •»
g parameters
lied to an op
ons are reduc
adsorber, de
**.*! •
|| |»



•g
8



S"
O
49
.




o

•g
e
o
o
o
49
U
9

L.
J

•)
«




"S
•
4?
4»


>
•8
£
4>
3
U
a
E
e

S

o
i
•
e
i a carbon ca
control device 1

















































_'
1
C
u
Q.
01
suppression and












































49
e

e

o
1
s

1 la returned
''Desorbed mater la


























8


e

2
49
i

o
49


^
1
JJ

U
49
49
C

3


C
~

L.
O
49
•
e
1
49
c
0
u
e
§
L.
O




i
49
C
•
*
X
0
U
u
9
O
m

1
u
JZ
J
!_
5
0.

"5

Ic
49

e

t>
u

jj
^
u
49
e
o
u
e
?

"•
1
o
c
o


^
c
^

8
e
*o
e.
49
e
O
u
a
c
49
X
4-75

-------
     Although the control types listed in Table 4-3 for the source category
are typically applicable to the source category, there may be site-specific
conditions that inhibit or prevent the use of a particular control type at
a particular facility.  Where there are several choices of control type
with equivalent levels of performance for a specific source category, pre-
sumably the facility operator would choose the lowest cost type to apply.
In some cases, there are significant differences in the costs of control
for similar performance levels, but factors such as waste incompatibility
or source size may prevent use of the least costly control.  For this rea-
son, "generic control devices" have been defined for tanks and waste fixa-
tion source categories for use in estimating nationwide emission reductions
and control costs.
     Table 4-4 defines the generic control devices used for the nationwide
impacts estimates.  Selection of the percentage weightings for each generic
control device was made on the basis of engineering judgment, taking into
account the application limitations of the different control technologies,
relative costs, and information about current industry practice.
     Venting a tank to an existing, on-site control device is generally
less expensive than using an internal floating roof or venting to a carbon
adsorber.  However, not all TSDF have an existing control device suitable
to receive the tank vent stream.  Depending on number of tank turnovers and
organic content of the waste, an internal floating roof will be less expen-
sive than venting to a carbon adsorber.  However, some wastes are not com-
patible with roof seal materials,-so the internal floating roof is not
always applicable either.  With a low number of tank turnovers and low
concentrations of low-volatility organics, carbon adsorbers can be cost-
competitive with internal floating roofs (details of estimated emission
reductions and control costs for the tank model units storing or treating
model wastes are presented in Appendixes C and H).  The percentage weight-
ings presented in Table 4-4 for tank generic control devices were selected
after considering the above factors.
     The selection of the percentage weightings for waste fixation is based
on TSDF site visits and contacts with TSDF operators.  This information
indicates that open pit fixation is the most frequently used waste fixation
                                    4-76

-------
               TABLE 4-4.  GENERIC CONTROL DEVICE DEFINITIONS3
Management process
 source category
Percentage
 weighting
       Control  technology
Quiescent (storage
or treatment) tank
   Uncovered
   Covered
   Waste fixation
    50
    25

    25

    50
    25

    25
    70

    30
Fixed roof plus internal  floating
roof
Fixed roof plus venting to carbon
canister or fixed-bed carbon
adsorber
Fixed roof plus venting to existing
control device
Internal floating roof
Vent to carbon canister or
fixed-bed carbon adsorber
Vent to existing control  device
Replace pit with mechanical mixer
vented to fixed-bed carbon
adsorber
Vent existing mechanical  mixer
to fixed-bed carbon adsorber
aThis table defines the combinations of control technology types used to
 estimate nationwide emission reductions and control costs for the listed
 source category.
bPercentage weightings show the percentages of each control option emission
 reduction and cost used to define overall emission reductions and costs
 for the particular combination of source category and control type.
                                     4-77

-------
process.  Consequently, it is estimated that 70 percent of existing TSDF

waste fixation operations will need to be converted to mechanical mixing-

type operations before add-on controls can be applied.

4.8  REFERENCES

1.    U.S. Environmental Protection Agency.  VOC Emissions from Volatile
      Organic Liquid Storage Tanks.  Background Information for Proposed
      Standards.  Office of Air Quality Planning and Standards.  Research
      Triangle Park, NC.  Publication No. EPA-450/3-81-003a.  July 1984.
      p. 3-3 through 3-6.

2.    Letter.  Anderson, R., Conservatek, to Kong, E., Research Triangle
      Institute.  June 2, 1988.  Aluminum dome roofs.

3.    Letter.  Roberts, J., Temcor, to Kong, E., Research Triangle
      Institute.  June 9, 1988.  Aluminum dome covers for tanks.

4.    U.S. Environmental Protection Agency.  Compilation of Air Pollutant
      Emission Factors.  Volume 1:  Stationary Point and Area Sources.
      Chapter 4.3.  Storage of Organic Liquids.  Office of Air Quality
      Planning and Standards.  Research Triangle Park, NC.  Publication No.
      AP-42.  September 1985.  p. 4.3-3.

5.    American Petroleum Institute.  Welded Steel Tanks for Oil Storage.
      API Standard 650, Seventh Edition.  Washington, D.C.  Revised
      February 1984.

6.    Memorandum from Johnson, W. L.  U.S. Environmental Protection Agency,
      Office of Air Quality Planning and Standards, to list of EPA addres-
      sees.  September 24, 1985.  VOC abatement for small storage tanks
      (draft).

7.    Reference 1, p. 3-6.

8.    Reference 1, p. 3-10 through 3-15.

9.    Reference 1, p. 3-6 through -3-9.

10.   Reference 1, p. 3-15 through 3-24.

11.   Reference 1, p. C-l through C-28.

12.   Reference 4, p. 4.3-3.

13.   Reference 1, p. 4-1 through 4-25.

14.   Reference 4, p. 4.3-3.
                                    4-78

-------
15.   Research Triangle Institute.   Trip report for Floating Membrane Cover
      Site Visit to Sonoco Products Company.   Prepared for U.S.  Environmen-
      tal Protection Agency,  Office of Air Quality Planning and  Standards,
      Research Triangle Park, NC.  June 27, 1989.

16.   Cadwallader, M.,  and M. Mathieson.  Large Scale Floating Cover
      Anaerobic Digesters:  Practical  with HOPE Geomembranes.  Gundle
      Lining Systems, Houston, TX.   April  1988.

17.   Gundle Lining Systems,  Inc.  Product Literature - Flexible Membrane
      Liners.  Received June 10, 1988.

18.   McCoy and Associates.  Air Supported Structure for Emissions Control.
      The Hazardous Waste Consultant.   November/December 1986.  p. 1-24.

19.   Hawk, C.  Air Bubble Enclosures  Cover More for Less.  Chemical Engi-
      neering.  May 9,  1988.   p. 83-85.

20.   Letter from Joffe, L.,  The Upjohn Company, to B. Watts, Chemical
      Manufacturers Association.  June 8,  1988.  Report for Chemical Manu-
      facturers Association on Air Inflated Lagoon Cover.

21.   Reference 19, p.  83.

22.   Reference 20.

23.   Reference 18.

24.   Research Triangle Institute.   Trip report for visit to Cecos Land-
      fill, Livingston, Louisiana.   Prepared for the U.S. Environmental
      Protection Agency, Office of Air Quality Planning and Standards.
      Research Triangle Park, NC.  September 12, 1986.

25.   Research Triangle Institute.   Trip report for visit to Chemical Waste
      Management, Inc., Sulphur, Louisiana.  Prepared for the U.S. Environ-
      mental Protection Agency, Office of Air Quality Planning and Stand-
      ards.  Research Triangle Park, NC.  September 12, 1986.

26.   Research Triangle Institute.   Trip report for visit to Michigan Dis-
      posal, Dearborn,  Michigan.  Prepared for the U.S. Environmental Pro-
      tection Agency, Office of Air Quality Planning and Standards.
      Research Triangle Park, NC.  May 29, 1987.

27.   U.S. Environmental Protection Agency.  Control Techniques for Vola-
      tile Organic Emissions from Stationary Sources.  (Draft report.)
      3rd ed.  Office of Air Quality Planning and Standards.  Research
      Triangle Park, NC.  March 21, 1986.  p. 3-7 through 3-74.
                                    4-79

-------
28.   Barnett, K., P. May, and J. Elliott.  Radian Corporation.  Carbon
      Adsorption for Control of VOC Emissions:  Theory and Full Scale Sys-
      tem Performance.  Prepared for U.S. Environmental  Protection Agency,
      Office of Air Quality Planning and Standards, Research Triangle Park,
      NC.  EPA Contract No. 68-02-4378.  June 6,  1988.   p. 3-1 through
      3-46.

29.   Joseph, G., T., and D. S. Deadlier.  Northrop Services, Inc.  APTI
      Course 415 Control of Gaseous Emissions—Student Manual.  Prepared
      for U.S. Environmental Protection Agency.   Research Triangle Park,
      NC.  Publication No. EPA-450/2-81-005.  December 1981.  p. 3-20 and
      p. 5-1 through 5-39.

30.   U.S. Environmental Protection Agency.  EAB  Control Cost Manual.
      Office of Air Quality Planning and Standards.  Research Triangle
      Park, NC.  Publication No. EPA 450/5-87-001A.  February 1987.  p. 4-5
      and 4-6.

31.   Research Triangle Institute.  Carbon Canister Monitoring.  Prepared
      for U.S. Environmental Protection Agency, Office of Air Quality Plan-
      ning and Standards.  Research Triangle Park, NC.   EPA Contract No.
      68-02-4326, November 23, 1988.

32.   Reference 28, p. 3-46 through 3-67.

33.   Reference 28, p. 3-34 through 3-38.

34.   Reference 28, p. 3-30.

35.   Research Triangle Institute.  Spent Carbon  Canister Management
      Options and Costs.  Prepared for U.S. Environmental Protection
      Agency, Office of Air Quality Planning and  Standards, Research
      Triangle Park, NC.  EPA Contract No. 68-02-4326, June 21, 1988.

36.  , Reference 27, p. 3-7 through 3-13.

37.   Memorandum with attachments from Farmer, J. R., U.S. Environmental
      Protection Agency, Office of Air Quality Planning  and Standards, to
      list of EPA addressees.  August 22, 1980.   Thermal incinerators and
      flares.

38.   Lee, K., J. L. Hansen, and D. C. McCauley,  Union Carbide.  Revised
      Model for the Prediction of Time-Temperature Requirements for Thermal
      Destruction of Dilute Organic Vapors and Its Usage for Predicting
      Compound Destructibility.  Presented at 75th annual meeting of the
      Air Pollution Control Association, New Orleans, LA, No. 85-5.3.  June
      1982.

39.   Midwest Research Institute.  Emission Test  of Acrylic Acid and Ester
      Manufacturing Plant,  Union Carbide, Taft, Louisiana.  Prepared for
      the U.S. Environmental Protection Agency, Office of Air Quality Plan-
      ning and Standards.  Research Triangle Park, NC.   EMB Report
      78-OCM-8.   September 1980.
                                    4-80

-------
40.
41.
42.




43.

44.

45.




46.



47.



48.

49.



50.



51.



52.
Midwest Research Institute.  Emission Test of Acrylic Acid and Ester
Manufacturing Plant, Rohm and Haas, Deer Park, Texas.  Prepared for
the U.S. Environmental Protection Agency, Office of Air Quality Plan-
ning and Standards.  Research Triangle Park, NC.  EMB Report
78-OCM-9.  August 1980.

Midwest Research Institute.  Stationary Source Testing of a Maleic
Anhydride Plant at the Denka Chemical Corporation, Houston, Texas.
Prepared for the U.S. Environmental Protection Agency, Office of Air
Qulity Planning and Standards.  Research Triangle Park, NC.  EMB
Report 78-OCM-4.  March 1978.

U.S. Environmental Protection Agency.  Distillation Operations in
Synthetic Organic Chemical Manufacturing-Background Information for
Proposed Standards.  Publication No. EPA-450/3-83/005a.  December
1983.  p. 4-21.

Reference 42, p. 7-6.

Reference 42, p. 4-31.

U.S. Environmental Protection Agency.  Parametric Evaluation of VOC/
HAP Destruction via Catalytic Incineration.   Project  Summary.
Research Triangle Park, NC.  Publication No.  EPA/600/52-85/041.  July
1985.  4 p.

U.S. Environmental Protection Agency.  Destruction of Chlorinated
Hydrocarbons by Catalytic Oxidation.  Washington, DC.  Publication
No. EPA-600/2-86-079.  September 1986.  p. 9.

MacKinnon, D. J.  Nitric Oxide  Formation at  High  Temperatures.  Jour-
nal of the Air  Pollution Control Association.  24(3):237-239.  March
1974.
Reference 42, p. 4-12 through 4-14.

U.S.  Environmental  Protection Agency.   Flare  Efficiency  Study.
Research Triangle  Park,  NC.  Publication  No.  EPA-600/2-83-052.
1983.   133  p.
July
 U.S.  Environmental  Protection  Agency.   Evaluation  of  the  Efficiency
 of  Industrial  Flares:   Test  Results.   Research  Triangle Park,  NC.
 Publication  No.  EPA-600/2-84-095.   May 1984.  178  p.

 Code  of  Federal  Regulations.   Title 40,  Part  60.18.   General  Control
 Device Requirements.   U.S. Government  Printing  Office.  Washington,
 DC.   July  1,  1986.  p.  218-219.

 U.S.  Environmental  Protection  Agency.   Evaluation  of  the  Efficiency
 of  Industrial  Flares:   Flare Head  Design and  Gas Composition.
 Research Triangle Park,  NC.  Publication No.  EPA-600/2-85-106.
 September  1985.   129  p.
                                     4-81

-------
53.

54.




55.




56.




57.




58.



59.

60.

61.



62.



63.


64.


65.


66.
Reference 42, p. 4-20 through 4-23.

U.S. Environmental Protection Agency.   Emission Test Report on  Ethyl-
benzene/Styrene, Amoco Chemicals Company, Texas City, Texas.  Office
of Air Quality Planning and Standards.  Research Triangle Park, NC.
EMB Report 79-OCM-13.  August 1979.

U.S. Environmental Protection Agency.   Emission Test Report on
Ethyl benzene/Styrene, U.S.S. Chemicals, Houston, Texas.  Office of
Air Quality Planning and Standards.  Research Triangle Park, NC.  EMB
Report 80-OCM-19.  August  1980.

U.S. Environmental Protection Agency.   Emission Test Report on
Ethylbenzene/Styrene, El Paso Products  Company, Odessa, Texas.
Office of Air Quality Planning and Standards.  Research Triangle
Park, NC.  EMB Report 79-OCM-15.  April 1981.

U.S. Environmental Protection Agency.   Organic Chemical Manufactur-
ing.  Volume 5:  Adsorption, Condensation, and Absorption Devices.
Research Triangle Park, NC.  Publication No. EPA-450/3-80-027.
December 1980.  p. II-2.

U.S. Environmental Protection Agency.   Air Pollution Engineering
Manual.  Research Triangle Park, NC.  Publication No. AP-40.  May
1973.  p. 189-198.

Reference 27, p. 3-63 through 3-74.

Reference 27, p. 3-52 through 3-63.

U.S. Environmental Protection Agency.   Process Design Manual for
Stripping of Organics.  Cincinnati, OH.  Publication No. EPA-600/2-
84-139.  August 1984.

Schweitzer, P. A.  Handbook of Separation Techniques for Chemical
Engineers.  New York, McGraw-Hill Book  Co.  1979.  p. 1-147 through
1-178.
Perry, R. H. (ed.).  Chemical Engineers' Handbook.  5th ed.
York, McGraw-Hill Book Co.  1973.  p. 13-1 through 13-60.
New
King, C. J.  Separation Processes.  New York, McGraw-Hill Book Co.
1971.  809 p.

Treybal, R. E.  Mass-Transfer Operations.  New York, McGraw-Hill Book
Co.  1968.  p. 220-406.

Berkowitz, J. B., et al.  Unit Operations for Treatment of Hazardous
Industrial Wastes.  Noyes Data Corporation.  Park Ridge, NJ.  1978.
p. 369-405, 849-896.
                                    4-82

-------
67.   U.S. Environmental Protection Agency.  Preliminary Assessment of
      Hazardous Waste Pretreatment as an Air Pollution Control Technique.
      EPA 600/2-86-028, NTIS PB46-17209/A6, March 1986.

68.   Exner, J. H.  Detoxification of Hazardous Waste.  Ann Arbor, MI, Ann
      Arbor Science.  1980.  p. 1-39.

69.   Metcalf and Eddy, Inc.  Briefing:  Technologies Applicable to Hazard-
      ous Waste.  Prepared for U.S. Environmental Protection Agency.  Cin-
      cinnati, OH.  May 1985.  Sections 2.9, 2.15, 2.16.

70.   Reference 63, p. 13-50 through 13-55.

71.   Reference 67, p. 45.

72.   Research Triangle Institute.  Field Test and Evaluation of the Steam
      Stripping Process at B. F. Goodrich, LaPorte, Texas.  Prepared for
      U.S. Environmental Protection Agency.  Cincinnati, OH.  Contract No.
      68-03-3253.  December 5, 1986.  91 p.

73.   Reference 67, p. 43.

74.   Allen, C. C., et al.  Research Triangle Institute.  Field Evaluations
      of Hazardous Waste Pretreatment as an Air Pollution Control Tech-
      nique.  Prepared for U.S. Environmental Protection Agency.  Cincin-
      nati, OH.  Publication No. EPA-600/2-86-048.  April 1986.  p. 63.

75.   Reference 61.

76.   Hwang, S. T., and P. Fahrenthold.  Treatability of Organic Priority
      Pollutants by Steam Stripping.  AIChE Symposium Series  197, Volume
      76.  1980.  p. 37-60.

77.   Reference 69, Section 2.16.

78.   Reference 66, p. 869.

79.   Reference 66, Section 2.16.

80.   U.S. Environmental Protection Agency.  Air  Stripping of Contaminated
      Water Sources-Air Emissions  and Controls.   Research Triangle  Park,
      NC.  Publication No. EPA-450/3-87-017.  August  1987.  125pp.

81.   Reference 66, Section 2.16.

82.   Reference 66, p. 869-880.

83.   Reference 74, p. 23.

84.   Luwa Corporation.  Product Literature--Luwa Thin-Film Evaporation
      Technology.  P.O. Box 16348, Charlotte, NC  28216.
                                     4-83

-------
85.   Harkins, S. M., et al.  Research Triangle  Institute.  Pilot-Scale
      Evaluation of a Thin-Film Evaporator for Volatile Organic Removal
      from  Petroleum Refinery Wastes.  Prepared  for U.S. Environmental
      Protection Agency.  Cincinnati, OH.  EPA Contract No. 68-02-3253.
      June  1987.  p. 2-1.

86.   Reference 74, p. 65-84.

87.   Reference 63, p. 13-50 through 13-55.

88.   Reference 62.

89.   Reference 63, p. 13-50 through 13-55.

90.   Reference 64.

91.   Reference 65.

92.   Reference 66.

93.   Reference 67.

94.   Reference 42.

95.   Reference 68, p. 3-25.

96.   Reference 69, Section 2.9.

97.   Allen, C. C.  Research Triangle Institute.  Hazardous Waste Pre-
      treatment for Emissions Control:  Field Tests of Fractional Distilla-
      tion at Plant B.  Prepared for U.S. Environmental Protection Agency.
      Cincinnati,  OH.  EPA Contract No. 68-02-3992, Work Assignment No. 35.
      January 1986.

98.   Reference 63, p. 19-57 through 19-85.

99.   Reference 63, p. 19-76.

100.  JACA Corporation.   Preliminary Assessment of Predictive Techniques
      for Filtration, Drying, Size Reduction, and Mixing Unit Operations.
      Prepared for U.S.  Environmental Protection Agency.  Cincinnati, OH.
      p. a-13 through a-14.

101.  Northeim, C.  Research Triangle Institute.  Summary of EPA/Chevron/
      API/RTI meeting on pretreatment of land treatable wastes for VO
      removal.  March 6,  1986.

102.  PEI Associates,  Inc.   Field Evaluation of a Sludge Dewatering Unit at
      a Petroleum Refinery.   Volume I.   Prepared for U.S.  Environmental
      Protection Agency.   Cincinnati, OH.  Contract-No. 68-02-3995.  May
      1988.   p. 6-28 through 6-29.
                                    4-84

-------
103.


104.




105.



106.

107.



108.

109.

110.


111.

112.



113.


114.



115.



116.



117.
 Ross,  R.  D.   The Burning Issue:   Incineration  of Hazardous  Waste.
 Pollution Engineering.   August 1979.   p.  25-28.

 Reed,  J.  C.,  and B.  L.  Moore.   Chapter 12,  Ultimate Hazardous  Waste
 Disposal  by  Incineration.   In:  Toxic and Hazardous Waste Disposal,
 Vol.  4.   Ann  Arbor,  Michigan,  New Ultimate Disposal Options,  Ann
 Arbor Science.   1980.   p.  163-173.

 Bonner,  T. ,A.,  et al.   Engineering Handbook for Hazardous Waste
 Incineration.  Monsanto Research Corporation.   Dayton,  OH.   EPA Con-
• tract No. 68-03-3025,  Work Directive SDM02.  June 1981.  p. 2-26.

 Reference 105,  p. 2-24.

 U.S.  Environmental Protection Agency.  Innovative Thermal Hazardous
 Waste Treatment Processes.  Cincinnati, OH.  Publication No.  EPA-
 600/2-85-049.  NTIS PB85-192847.  April 1985.   p. 55.

 Reference 105,  p. 2-30.

 Reference 105,  p. 2-32.

 Sittig,  M.  Incineration of Industrial Hazardous Wastes and Sludge.
 Noyes Data Corporation.  Park Ridge, NJ.   1979.

 Reference 107.

 Code of  Federal Regulations.  Title 40, Part 264.343.   Incinerator
 Performance Standards.  U.S.  Government Printing Office.  Washington,
 DC.  July 1.  1986, p.  533-534.

 U.S. Environmental  Protection Agency.  Petroleum Refinery  Enforcement
 Manual.   Research Triangle Park,  NC.   January 1980.  p. 4.13-1.

 U.S. Environmental  Protection Agency.  Hazardous Waste  Management
 System;  Burning of  Waste Fuel and Used Oil  in Boilers  and  Industrial
 Furnaces:  Final  Rule.  50 FR 49164-71.  November  28,  1985.

 Trip report.  Research  Triangle  Institute.  Visit  to Mobil Oil  Cor-
 poration, Joliet  Refinery, Joliet,  IL.   Prepared for U.S.  Environmen-
 tal  Protection  Agency.  September 4,  1986.

 Telecon.  Wright, Milton D.,  Research  Triangle  Institute,  with
 Weisenborn,  Bill, Conoco,  Inc.   June  19,  1986.   Coking  of  refinery
 sludges.

 Radian Corporation. Field Assessment  of Air  Emissions  and Their  Con-
 trol at  a Refinery  Land Treatment Facility: Project Summary.   Pre-
 pared for U.S.  Environmental  Protection  Agency.  Cincinnati,  OH.   EPA
 Contract No. 68-02-3850.   September 12,  1986.   17  p.
                                     4-85

-------
 118.   Weitzman,  L.  (Acurex Corporation).   Organic Air Emissions  from Waste
       Stabilization.   Prepared for U.S.  Environmental  Protection Agency,
       Risk Reduction  Engineering Research Laboratory,  Cincinnati,  Ohio.
       Contract No.  68-02-4285,  Work Assignment No.  1/016.   January 30,
       1989.   24 p.

 119.   Research Triangle  Institute.   Characterization  of Nationwide Waste
       Fixation Practices  for Facilities  Subject to  RCRA Subtitle C.
       Prepared for  the U.S.  Environmental  Protection  Agency,  Office of Air
       Quality Planning and Standards,  Research Triangle Park,  NC.
       August  17,  1989.   15 p.

 120.   Weitzman,  L., L. Hamel,  and  S. Cadmus  (Acurex Corporation).   Volatile
       Emissions  from  Stabilized Waste.   Prepared for  U.S.  Environmental
       Protection  Agency,  Hazardous  Waste  Engineering  Research  Laboratory,
       Cincinnati, Ohio.   Contract  No.  68-02-3993, Work  Assignments No. 32
       and  37.   September  1987.   125 pp.

 121.   Acurex  Corporation.   Trip report for visit to Michigan  Disposal.
       Prepared for  the U.S.  Environmental  Protection  Agency,  Risk  Reduction
       Engineering Research Laboratory, Cincinnati,  Ohio.   June 6,  1989.

 122.   Acurex  Corporation.   Trip report for visit to S & W  Waste,  Inc.
       Prepared for  the U.S.  Environmental  Protection  Agency,  Risk  Reduction
       Engineering Research Laboratory, Cincinnati,  Ohio.   June 6,  1989.

 123.   Acurex  Corporation.   Trip report for visit to Chem-Met  Services.
       Prepared for  the U.S.  Environmental  Protection  Agency,  Risk  Reduction
       Engineering Research Laboratory, Cincinnati,  Ohio.   June 6,  1989.

 124.   Acurex  Corporation.   Trip report for visit to Stout  Environmental.
       Prepared for  the U.S.  Environmental  Protection Agency,  Risk  Reduction
       Engineering Research Laboratory, Cincinnati,  Ohio.   June 22,  1989.

 125.   Acurex  Corporation.  Trip  report for visit to GSX  Services,  Inc.
       Prepared for  the U.S.  Environmental  Protection Agency, Risk  Reduction
       Engineering Research Laboratory, Cincinnati,  Ohio.   June 22,  1989.

 126.   Research Triangle Institute.  Trip report  for site visit to  Solidtek
       Systems, Inc.  Prepared for the U.S. Environmental Protection Agency,
      Office of Air Quality  Planning and Standards, Research Triangle Park,
       NC.  August 3, 1989.

127.  Reference 123.

128.  Reference 126.

129.  U.S.  Environmental  Protection Agency.  Fugitive Emission Sources of
      Organic Compounds—Additional Information  on  Emissions,  Emission
      Reductions, and Costs.  Office of Air Quality Planning and Standards.
      Research Triangle Park, NC.  Publication No.  EPA-450/3-82-010.  April
      1982.  p. 2-21.
                                    4-86

-------
130.  Reference 129, p. 4-1 through 4-75.

131.  U.S. Environmental Protection Agency.  VOC Fugitive Emission Sources
      in Synthetic Organic Chemicals Manufacturing Industry—Background
      Information for Proposed Standards.  Office of Air Quality Planning
      and Standards.  Research Triangle Park, NC.  Publication No. EPA-
      450/3-80-033a.  November 1980.  p. 4-1 through 4-27.

132.  Reference 114.
                                     4-87

-------

-------
                           5.0  CONTROL OPTIONS

     The purpose of this chapter is to describe control options considered
in the selection of a basis for air emission standards to be proposed for
treatment, storage, and disposal facilities (TSDF) under Section 3004(n) of
the Resource, Conservation, and Recovery Act (RCRA) as amended.  In addi-
tion, this chapter describes the "baseline" against which the nationwide
impacts of control options were measured.
     Five specific control options are described.  These options are based
on the use of add-on emission controls applied to individual emission
sources.  The estimated human health and environmental impacts of these
five options are presented in Chapter 6.0.  Cost impacts are presented in
Chapter 7.0, and economic impacts^are presented in Chapter 8.0.  The option
selected as the basis for the proposed standards, and the factors leading
to the selection of that option, are discussed in the preamble to the
proposed standards published in the Federal Register.
5.1  CONTROL OPTION CONCEPT
     As discussed in Chapters 3.0 and.4.0, there are a variety of sources
of organic emissions at TSOF and several types of emission controls that
can be applied to many of these sources. The term "control option," as used
here, refers to a unique combination of emission sources, emission
controls, and action levels for applying the controls.  Different options
are developed and evaluated to estimate the impacts of potential
regulations.  It is important to recognize, however, that although a
control option identifies specific emission controls to be applied to TSDF
sources, a regulation written to implement the option may be in terms of
performance standards that allow equivalent, or more effective, controls
for compliance.  The emission sources, controls, and action levels
considered in developing control options, the selection of control options
                                    5-1

-------
 for  detailed evaluation, and the  impacts to be estimated for each option
 are  discussed  in the following sections.
 5.2   EMISSION  SOURCES, CONTROLS,  AND ACTION LEVELS CONSIDERED IN
      DEVELOPING CONTROL OPTIONS
 5.2.1  Emission Sources
      TDSF emission source categories are shown in Table 5-1.  Hazardous
 waste management processes with similar emission characteristics and
 potential emission controls are grouped together (e.g., storage and
 treatment quiescent tanks are combined into one source category).  Land-
 fills, wastepiles, and land treatment are shown grouped together under the
 category of "Land Disposal Units."  This is because hazardous wastes
 entering these types of waste management units are regulated by the land
 disposal restrictions (LDR), which require treatment of a waste with best
 demonstrated available technology (BOAT) before it is placed in one of
 these units.   It is presumed that this treatment will decrease the organic
 air  emission potential of landfills, wastepiles, and land treatment, and
 therefore additional air emission controls for these sources were not
 considered in  developing regulatory options.  This presumption will be
 reviewed after all requirements under the LDR program are promulgated.
 Similarly, control of organic air emissions from ancillary equipment
 (pumps, valves, flanges, etc.) and certain process vents at TSDF is
 required by a  separate rulemaking under RCRA Section 3004(n) proposed on
 February 5, 1987 (52 FR 3748), and therefore additional controls for these
 sources were not considered.  More information on the LDR and the standards
 for  emissions  from equipment leaks and process vents is presented in
 Section 5.4.2.
     Surface impoundments are also covered by the LDR, but are exempt from
 LDR  requirements under certain conditions.  Those' impoundments not covered
by the LDR would continue to have significant potential air emissions and,
therefore, additional controls for surface impoundments are being con-
sidered under  RCRA Section 3004(n).
5.2.2  Controls
     As described in Chapter 4.0,  there are a variety of control techniques
available to reduce organic air emissions from TSDF.  These include the
                                     5-2

-------
                TABLE 5-1.  TSDF EMISSION SOURCE CATEGORIES
                              Source category
                  Quiescent tanks (storage or treatment)

               Quiescent impoundments (storage or treatment)

                            Non-quiescent tanks

                        Non-quiescent impoundments

                                Containers9

                           Waste fixation units

            Ancillary equipment (pumps,  valves, flanges, etc.)b

                                  SpillsC

                       Hazardous waste incineration^

     Land disposal units:  Landfills, wastepiles, and land treatment6


TSDF = Treatment, storage, and disposal  facilities.

alncludes loading and storage.  Containers are any portable device in
 which a material is stored, transported, treated, disposed, or otherwise
 handled.

^Separate standards for equipment leaks were proposed February 5, 1987
 (52 FR 3748).

cSpills are regulated by 40 CFR Part 264, Subparts D and J, and by Part
 265, Subparts D and J.

^Air emissions from hazardous waste incinerators are regulated by 40 CFR
 Part 264, Subpart 0.

eAll hazardous wastes placed in these sources must meet pretreatment.
 requirements of the land disposal restrictions.
                                    5-3

-------
addition of engineering controls, such as covers and add-on control
devices, and the use of waste treatment processes to remove organics
directly from hazardous waste, thus reducing its air emission potential
prior to placement in a waste management unit.
     In selecting controls to serve as the bases of regulatory options, EPA
considered how the standards being developed for air emissions would fit
into the broad framework of regulations that affect the management of
hazardous waste at TSDF.  Regulations are currently in place, or are being
developed, that are directed at hazardous waste disposal.  These include
the LDR, standards for equipment leaks and process vents from treatment
processes, and standards for hazardous waste incinerators.  In addition,
RCRA-exempt wastewater treatment units are being addressed under the Clean
Air Act.  All of these regulations are designed to act together to protect
public health and the environment from exposure to pollutants via both
ground water and air from waste disposal units.
     Considering that all hazardous waste must ultimately be disposed and
that the LDR ensure that air emissions generated by hazardous waste
disposal practices will be controlled, EPA has adopted a regulatory
philosophy of emission containment for TSDF sources that manage waste prior
to waste disposal.  Under this philosophy, the focus is on applying
controls that reduce the volatilization of organics from hazardous waste
prior to disposal, where organics will either be destroyed or removed from
the waste by treatment processes that are controlled for air emissions.
     Consistent with the objective of containing potential organic emis-
sions from hazardous waste prior to its disposal, the regulatory options
selected for detailed evaluation as possible bases for standards involve
primarily the use of suppression (covers)  or suppression plus add-on
control devices.  However, this will not necessarily preclude the use of
other,  equally or more effective controls  to meet the requirements of the
proposed regulation.  For example,  each of the options under consideration
consists of a combination of controls applied to TSDF emission sources plus
an action level  above which the controls must be applied.  By incorporating
an action level, each option would  implicitly allow an owner or operator to
use a waste treatment process to reduce the organic content of the waste
                                     5-4

-------
managed to below the action level, in which case additional controls would
not be required by the air standards.
5.2.3  Action Levels
     To apply emission controls to waste management processes with regard
to the emission potential of the wastes managed, the regulatory control
options developed for TSDF air emission standards include an "action level"
above which controls must be applied.  Action levels can be used as a
mechanism for prioritizing emission sources within a waste management
facility for control and for excluding sources that have lower emission
potential.  Action levels can be expressed in several formats (e.g., in
terms of volume throughput, capacity, or measured or calculated emissions).
An action level based on waste volatile organic concentration (as measured
by an appropriate test method) is appropriate for TSDF sources such as open
tanks, surface impoundments, containers, and waste fixation, where hazard-
ous waste can be exposed directly to the ambient air, sunlight, and wind.
For completely enclosed sources, such as covered quiescent tanks, a more
appropriate indicator of emissions, and thus a more appropriate format for
an action level, is the vapor pressure of the waste.
      In developing control options for TSDF air emission standards, EPA
incorporated two types of action levels.  For all sources except covered
quiescent tanks, the action level associated with the option is based  on
the volatile organic content of the waste at the point of generation.  For
covered quiescent tanks, the action level above which additional controls
(e.g., vent to control device) would be required is based on the vapor
pressure of the waste contained in the tank.
5.3   SELECTION OF CONTROL OPTIONS
      Five control options were selected for detailed evaluation that
illustrate the various combinations of action levels and controls that
could be applied to TSDF emission sources.  All of the options selected
would be expected to result in significant reductions in organic emissions,
and associated human health and environmental impacts.  They are also  used
in later chapters to illustrate how the impacts of TSDF control options  are
estimated.  These five options are described in Table 5-2.
                                      5-5

-------



















i
*-«


1


5
§
uj
3
£C
H*
*
f4
t
Ut
ta
t-













£ IL
ia"S 0-
lei
llf




co.
o e S
1|:




11
« * Gb

c "° S
4* •—

e*>




«Jt
•2i

'a^.
e a./>.
-s



s~
IK

Source category
u









„
i
c
8
5
4>
|
,3









•
,3

0
T>
L.
49
O
U
5
4>
C
;
»
1


„
1
5
4>
C
a
3
Quleicent tanka
(atorage or treatment)

£

C
8
o
+»
•
..
3 .


£ £
49 49
i §
U U
5 5
4> 4>
1 J
i i
O O
u u

^
L.
i
U
5

4>
C


; 1
6* 6*


^ *o
L. t.
49 *>
O O
U U
o a
49 49
4> 4>
c c
s s
„ .
s s
3 3



o o
1> t.
4» 49
C C
8 8
5 5
4> 4>
I S
t fe
s i
u u
Quleicent lapoundnents
(atorage or treatment)
Non-quleacant tanka
""a
£ 5
49 •
C 0
^
o a
•a 0)
i i
> 3
5 !
3 3

'o
1 1
I -
O "S
4» O)
! 1
a e
3 3
^
a
— C
•
^
i
L.
J"
a


e
. u

'o
£ 1
1 J
5 I
e 1

A
L L
e e
3 3


1,
o 5
1 1
•r. vent to co
»r/aubmargad 1
> >
o 6*
Non-quiescent iMpoundmenta
Containers

"o
i_
4*
C
o
u
5
- i : : ;
>
o


~Q
L.
49

£
^ ill!
>

,

-
.
»
i t i i
ttii




<


49
C
O
u
5
- : : : i
c

.
3



I
8
5
3
i ^
1 §
1 ? •:
0 • • 0 •
1 ££• ^ 1
X 3 • »*. U •—
= 8z J S '
.— ^ •« ^
e u u — u e
•u e c a c «
S 5< " « -"







































|
S
1
•5
-o
e
TSDF = Treatment, storage.
VO = Volatile organlca.



4>
O
c
—
*>
1
m
L.
a
4>
|
U
5
c
|
U
u
£
u
1
e
o
u


*;
•o
•
49
•
|

•
49
U
el
1

* —
i:
• o
=r
— a.

^fe
e*"
• «
11
£1
tl
•1
^ 0.
11
*T
. 11
1 i!
I „"
• ?^
4> **.-
Je L.
u •
49 •
II • •
' ll
•

.

C

49
!
§•
l
>
3
j>
J
O
C
:
49
e ^
•v*
ji m
1:
11
•1


?:
3 0
• *^

t.
e*a
.?*
— e
— L.
u e
ii
?!
L. e

a4*
11
>«-
•*• c
0 JO
c u
!l
^0
"Action level Is based on v
If volatile organic contan



u
j

£
1
U
a
5

J
e
a
|
i
^
e
u
E
o

c
0


3


N

iu>
Is

waste 1
greater

0 0
4> O
e 49
5-
c a
O 3

ie
e L
:l
3fe
a a
0?
f 4>
M
cQulescent tanks must be co
when the waste In the tank



























L.
5
| -:
fe S
a
III

IV 3
t e -
e o 10
> o «o
O L N
u a

? s •
i •£ 8
O •
• Z "
14 J
•o e §
c
• 1. T>
§<2I
•° •£ a
L. • •
dSubmarged fill required fo
•Required by TSDF air stand
'Thla source currently Is r































0
u

u>

s
CM
TI
c
•
S
C4
£
U
ated under 40
id treatment.
i-5
Bthia source currently la r<
hUndfllla. wastepllas. and
5-6

-------
     Options 1, 2, 4, and 5 are distinguished from one another by the
number of sources requiring control; the number of sources requiring
control is determined by the volatile organic concentration action level.
In control option 1, the concentration action level is 0;  that is, controls
would be required on all waste streams containing detectable amounts of
volatile organics.  For control options 2, 4, and 5, the concentration
action levels are 500 ppm, 1,500 ppm, and 3,000 ppm, respectively.  Unless
it is demonstrated that the waste being handled is below the volatile
organic concentration action level, all of the following controls would be
required:  (1) covers or enclosures and submerged loading techniques would
be required to control emissions from container loading operations and for
dumpsters, (2) covers and control devices would be required for surface
impoundments, and (3) covers and control devices would be required for
tanks unless the tank is non-aerated and it is demonstrated that the vapor
pressure of the waste in the tank is below the vapor pressure action level.
In this case, covers alone would be required.  If an owner or operator
wishes to demonstrate that the vapor pressure of a waste stream is below
the vapor pressure action level, he would have to perform a vapor pressure
test using an appropriate test method.
     The types of covers that could be used on tanks to meet the standards
include fixed roofs, internal floating roofs, and external floating roofs.
Covers that could be used for surface impoundments include air-supported
structures.  Control devices that could be used include carbon adsorption
units, vapor incinerators, and flares.
     Control option 3 has an action level of 500 ppm, the same as option 2,
but differs from the other options in that covers alone may be used on non-
aerated tanks and surface impoundments without the need for a vapor
pressure test.  The controls specified for this option are the same as
described above for all sources except non-aerated surface impoundments and
non-aerated tanks.  Under this option, non-aerated surface impoundments
could use floating synthetic membranes as a means of complying with the
proposed standard.
     The nationwide impacts that will be estimated for control options
selected for detailed evaluation and the baseline to which the impacts of
options will be compared are discussed below.
                                    5-7

-------
 5.4  BASELINE FOR NATIONWIDE IMPACTS ESTIMATES
      The baseline provides a perspective from which the impacts of adopting
 control options can be evaluated.  Chapter 3.0 of this document presents
 nationwide uncontrolled TSDF organic emissions; i.e.,  emissions with  cur-
 rent existing controls and before the adoption of additional  nationwide
 control requirements.  However,  there are regulations  that affect  TSDF air
 emissions that are, or will be,  in place when the RCRA 3004(n)  standards
 being developed in this rulemaking are promulgated. The baseline  against
 which the potential impacts of the 3004(n)  standards are measured  should
 reflect these other regulatory requirements if they affect TSDF nationwide.
      Federal  regulatory requirements that affect TSDF  nationwide include
 the land disposal  restrictions (proposed and promulgated under  RCRA Section
 3004(m))  and  TSDF  air standards  for process vents and  fugitive  emissions
 (proposed February 5,  1987,  under RCRA Section 3004(n)).   There are other
 Federal  requirements  applicable  to TSDF,  such as the RCRA Corrective  Action
 Program (implemented  under RCRA  Section 3004(u)),  but  these are site-
 specific  rather than  nationwide  control  requirements.
      Also, there are  standards that apply to TSDF emission sources  at the
 State level.   However,  these are limited  and vary widely  from State to
 State.  A survey of State  programs indicated that 12 States have estab-
 lished  generic volatile organic  compounds (VOC)  standards  that  might  affect
 TSDF  emission  sources.   Thirty States  have  standards applicable to  storage
 tanks,  17  States have  standards  for terminal  loading,  and  9 States  have
 standards  for  hazardous  waste  landfills.  For those States that do  have
 standards, there are differences  in  how VOC  is  defined, making  it difficult
 to compare requirements  from State to  State.
      After the review  of Federal  and State  standards applicable to  TSDF,  it
was concluded  that  the  baseline  for  the RCRA Section 3004(n)  standards
 under development should reflect  the impacts  of  the LDR and the TSDF  air
standards for  process vents  and equipment leaks.   Due  to the  limited
applicability  and lack of uniformity in State  standards, they should  not be
included in the  baseline.
     More information on how the  impacts of  the  LDR  and the TSDF process
vent and equipment  leak standards will be simulated  in the  baseline is
presented below.
                                    5-8

-------
5.4.1  Land Disposal Restrictions
     The Hazardous and Solid Waste Amendments (HSWA) of 1984 mandate a
number of actions that EPA must take to reduce the threat of hazardous
waste to human health and the environment.  These actions include
restricting hazardous wastes from land disposal.  The EPA is currently
developing regulations (referred to as "land disposal restrictions") that
will require that hazardous wastes be treated to reduce concentrations of
.specific chemicals or hazardous properties before the waste may be placed
in a land disposal unit.  The affected land disposal units include surface
impoundments, wastepiles, landfills, and  land treatment operations.
Surface impoundments used for treatment of hazardous wastes are exempt from
the LDR if treatment residues are removed annually.  The waste treatment
technologies required to reduce chemical  concentrations before land
disposal are referred to as best demonstrated available technologies
 (BOAT).  The restrictions express BOAT as a performance standard that
requires wastes  to be treated before entering a  land disposal unit  (to
reduce the waste's toxicity or mobility). The wastes must be treated to
levels that can  be achieved by use of the best technologies commercially
available.
     The EPA is  developing the LDR in stages.  Waste-specific prohibitions
on  land disposal  have been promulgated for certain  spent solvent wastes  (40
CFR 268.30); dioxin-containing hazardous  wastes  (40 CFR 268.31); the
 "California  list" wastes  (40 CFR 268.32); the  "First Third" set of  listed
wastes  (40 CFR 268.33); the  "Second Third" set of  listed wastes  (40 CFR
268.34); and,  recently, the  "Third Third" set of listed wastes  (55  FR
 22520, June  1,  1990).  The TSDF  air emission standards being developed in
 this current rulemaking would be promulgated after the date that LDR are  in
 effect  for  all wastes  identified or  listed as  hazardous as of November 8,
 1984.   Therefore,  the  LDR  are considered  a part  of the baseline  against
 which  the  potential  impacts  of the 3004(n) standards  are measured.
     The  LDR for many  listed wastes have  only  recently been finalized and
 many of the  treatment  standards  are expressed  as performance standards for
 certain  constituents in  the  treatment  residue  rather than  as specific
 technology  requirements.   Therefore,  EPA  is  not  certain  at this  time as  to
                                      5-9

-------
how the LDR will ultimately impact TSDF air emissions.  For the nationwide
impacts analysis, EPA first needed to forecast the approaches TSDF owners
and operators would most likely choose to implement the LDR for specific
wastes types.  Using available information, EPA made certain assumptions
regarding the general or average response of the hazardous waste management
industry to compliance with the LDR.  The following assumptions were
developed concerning the manner in which TSDF will respond to the restric-
tions for purposes of estimating overall baseline impacts for the air
standards:1
     •    All wastes currently land-treated (except organic-containing
          solids) will be incinerated.  Solids will be fixated.
     •    All organic liquids and sludge/slurries that are currently
          sent to landfills and wastepiles will be incinerated or
          steam-stripped.
     •    All dilute aqueous liquids and aqueous sludge/slurries are
          fixated and landfilled.
     •    All surface impoundments will continue to operate as
          impoundments and be dredged annually or will be converted to
          uncovered tanks.  In both cases, it is assumed that there
          will be no change in emission, emission reductions, or cost
          of control.
     •    All fixation processes will yield a solid waste product
          rather than a nonliquid such as sludge.  This assumes an
          increase in the degree of fixation that will increase emis-
          sions from the treatment process.
     The technology assumptions listed above may not be sufficient to
comply with the LDR treatment standards for all TSDF.  However, on a
nationwide basis, it is likely that they represent the general or average
response of the hazardous waste management industry.  Therefore, it is a
reasonable basis for the calculation of baseline emissions against which
the nationwide impacts of potential air standards under RCRA Section
3004(n) are evaluated.
5.4.2  TSDF Air Standards for Equipment Leaks and Process Vent Control
     To address concerns about air emissions from the treatment processes
expected to be used to comply with the land disposal restrictions, EPA
promulgated air emission standards under RCRA Section 3004(n) to reduce
                                    5-10

-------
organic emissions vented from the treatment of hazardous wastes by
distillation, fractionation, thin-film evaporation, solvent extraction,
steam stripping, and air stripping, as well as from leaks in certain piping
and equipment used for hazardous waste management processes (55 FR 25454,
June 21, 1990).  Sources of process vent emissions from treatment units
include process condenser vents, and distillate receivers, surge control
vessels, product separators, and hot wells, if process emissions are vented
through these vessels.  Equipment leak sources include pumps, valves,
pressure-relief devices, compressors, open-ended lines, and sampling
connections.  These standards apply to hazardous wastes containing greater
than 10 percent organics.  Specific requirements include reduction of
process vent emissions to less than 1.4 kg/h  (3 Ib/h) and 2.8 Mg/yr  (3.1
tons/yr) or  reduction of facility process  vent emissions by 95 percent;  and
a  leak detection and repair program for equipment  leaks.
     To simulate the impact of these standards on  the baseline, all  process
vents and equipment leak emissions at facilities handling wastes containing
greater than 10 percent organics are assumed  to be controlled  as part  of
the baseline.
5.4.3  New Source  Performance Standards  (NSPS) for Volatile
       Organic  Storage Vessels
     Under the  authority of the Clean Air  Act, EPA has  promulgated
standards of performance in 40 CFR Part  60 for storage  vessels that  contain
volatile organic  liquids (VOL), and that are  constructed  or modified after
July 23, 1984.  These  standards require  that  tanks larger than 75 m3 (about
20,000  gal)  containing VOL  be equipped with air pollution  controls  if  the
vapor  pressure  of the  stored organic  liquid is greater  than  the  specified
 levels.  The controls  required  by  the standards are  shown  in  Table  5-3.
     The EPA views the controls  required by the NSPS as minimum  controls
 for any large  tank containing organic hazardous waste,  regardless of the
 date of construction  of  the tank.  Accordingly, the  NSPS control  require-
ments  for  VOL  storage vessels are  included as minimum baseline control
 requirements for tanks in  the standards  proposed  for hazardous waste TSDF
 under  RCRA Section 3004(n). An exception  to  this is the NSPS requirement
 for any tank greater than  75 m3 and  containing  an organic liquid with  a
 vapor  pressure greater than 76.6  kPa.   This requirement is not included in
                                     5-11

-------
        TABLE 5-3.  CONTROL REQUIREMENTS UNDER THE CLEAN AIR ACT FOR
                  VOLATILE ORGANIC LIQUID STORAGE VESSELS3
Tank size
 Vapor pressure
of stored liquid
       Controls required
From 75 m3 up to
151 ra3

(from 19,789 to
 39,841 gal)
From 27.6 kPa to
    76.6 kPa
                    Equal to or
                    greater than
                      76.6 kPa
One of the following:

(1) Fixed roof plus internal
    floating roof;

(2) External floating roof;

(3) Closed vent system plus a
    control device; or

(4) A system equivalent to those
    described in  (1) - (3).

A closed vent system plus a
control device.
Equal to or
greater than
151 m3

(greater than
 39,841 gal)
From 5.2 up to
   76.6 kPa
                    Equal to or
                    greater than
                      76.6 kPa
One of the following:

(1) Fixed roof plus internal
    floating roof;

(2) External floating roof;

(3) Closed vent system plus a  •
    control device; or

(4) A system equivalent to those
    described in (1) - (3).

A closed vent system plus a
control device.
aSource:  40 CFR Part 60, Subpart Kb.
                                    5-12

-------
the proposed TSDF standards because EPA does not expect wastes managed at
TSDF to have vapor pressures near or above this value.
     The EPA believes that most existing tanks at TSDF are smaller than the
sizes regulated by the NSPS for VOL storage vessels.  Consequently, includ-
ing the NSPS requirements for VOL storage in the proposed standards for
TSDF under RCRA 3004(n) should have little or no additional impacts.
However, making the NSPS control requirements part of the baseline for the
TSDF standards would ensure that any existing large tanks used for the
management of hazardous waste at TSDF are controlled at least as effec-
tively as new tanks.
5.5  REFERENCE
1.   Industrial Economics, Inc., and ICF Incorporated.  Regulatory Analysis
     of Proposed Restrictions on Land Disposal of"Hazardous Wastes.  Pre-
     pared for U.S. Environmental Protection Agency.  Washington, DC.
     December 27, 1985.  p. 4-20 through 4-22 and exhibits.
                                     5-13

-------

-------
          6.0  NATIONAL ORGANIC EMISSIONS AND HEALTH RISK IMPACTS

     The nationwide organic air emission and health risk impacts associated
with each of the treatment, storage, and disposal facility (TSDF) control
options identified in Chapter 5.0 are discussed in this chapter.  The
primary emphasis of Chapter 6.0 is to present the approach for assessing
these impacts by using the control options as a guide for discussion and
presentation.  Both beneficial and adverse environmental impacts are
assessed.  Table 6-1 summarizes these nationwide impacts; presented are the
nationwide estimates of TSDF organic emissions, cancer incidence, and maxi-
mum lifetime risk for the five control options as well as the uncontrolled
and baseline scenarios.  Comparisons to the baseline situation are also
made to provide a relative measure of the effectiveness of or degree of
control required under the five options.  More detailed information on the
emissions and health risks associated with implementation of the control
options are provided in Sections 6.1 and 6.2.  The nationwide emission
reduction for each control option is tabulated in Section 6.1.   Impacts  on
human health, assessed as cancer incidence and maximum lifetime  risk of
contracting cancer, are presented in Section 6.2.  Impacts on water qual-
ity, solid waste, energy, and other environmental concerns are presented in
Section 6.3.
6.1  ORGANIC EMISSION  IMPACTS
     This section presents the nationwide impacts on TSDF organic air emis-
sions for five control options and  includes a description of how emissions
under the uncontrolled, baseline, and controlled scenarios were  estimated.
A tabular presentation of the estimated emission reductions from affected
waste management units is also included.  As discussed  in Chapter 5.0, the
baseline case assumes  that Resource Conservation and Recovery Act  (RCRA)
land disposal restrictions and the  1987 proposed TSDF  air emission
                                     6-1

-------












§
u.

1
3
n

U)
M
ce

3« "

_J Z
^C C3
id M

OL
§ °
o
tQ Ft*

o is
M O
tf) »
"S 0>
u n o
• c
0 >O 0
o-o
c E —
0 O O
t> L. C
U
C
M




U t-
.T *»
. •. ">
t- o *
0 C 0
0 0 C
C t> 0
• — -o
o o —
c u
•™ c
*~




49 •»
e c
0 O
U BW
L. 49
0 U
a. 3

L.

c
o
"•8 2 «.
3 — >»
28*
a
c jsco
OQ
•r S 1-1
n o
n (-
.- *.
l3


*-0
A t.
J-5
*•* CO
JS




n
•
u
o
49
C
O
u

•

ls> *o 1> !> 1) 1> 1>

X X X X X X X
CM CM to to to co en









t& O Q (& O
1 1 CO CO CO CO CM














«•«••»
* • »
O O IO CD 00 ^ QD
co ^r i-« t-i







,


ID IO CO CM «S
I i 01 o> o> 0) cn
1 1







§5. B <9 O
S f- CO CM
i i r>- r- co to co










§G> CM CO 5) O 19
S cn co eo T oo
CO 00 i-« t-» -H
r< iH







"O
0
— -o
O 0 tH CM CO ^ U>
49 — C C C C C
e — o o o o o
O 0 •— •— *~ *~ •••
U » 49 49 49 49 49
c • a. a. a. a. a.
O CD O O O O O
I


















































^
49
"o
m
^
a
V)
o
a.
VI
•o

•o
c
a
i
a
L. •
3-
a
« o

c —
go.
0.
49 a
a
0 49
II II

U. 1
O 1
{2


0 "
49 C

0 49
C
0 0
en u

i. -
O 1)
49 49
a> c


e»T3
jc c
C 3
a o
*!

c
0 49
U C
to 0
0 U

"5 0
o~>~
3
cr

« c
0 O
"t.
o -
O) M

49 C
a a
U 49
0 49
u c
L. 0
3 U
O IA
IA 0

LL 3
Q cr
CO 1

o
en c
c
04?

l|
0 0
JC (.
49 49
O) U
C O
— 0
~~ O
o a
U L.
«|j O
O 0)
o ^^

§w
49
i. c
en -o M
49 C 49
O 3 —
a o c

o
M 49 —
* C 49
o 0 a
.cox
IA n —
O c^
0 —
— 30
.O O~49
a IA
49 > a

« 49"
— c-o
a"

















































O
u
3
O
(A
X
-O
IA
C
O
M

'I
0

0
•o
*"—
*
0

49
a
c
L.
O

CM
1
CO

0

a
t-
3
!•
0

ja











































0

L.
3
O
ei

2
0
o
0
"O
*o
c
1.
0
u
c
a
u

.g
•^
^
c
o

49
a
c
o

*?
CO

0
J3
a
1-
o
49
i.
0
«*-
0
6r

49
O I
"0 a 0 a 49
> X I.Q. C
0 — 49 Jt 0
— t- 0
49 CO Bl
C 0 C • 0
O 49 0 B —
— M U fH 3
49 a n cr
o » 0 01
a — ~o -o
O> 3 0 C
0 c cr 0 a
jjj ,M y
49 -O-O X 0
3 C 0 O>
c— a a
• U -92 L.
«C C 0 C O
49 — O) a 49
^ a 49 ei
t. t.
0 0> O 0-O
49 JC 49 JC 0
a c IA 49 i.
• a 0
t- 49 -O C >
en 0— o
I- L. U
e> o 0 0
e«t- > 49 o
O O 01 49
— in o a
49 0 JT3
not. 0
L. — O 0 —
49 > u. j: —
c 0 49 a
0 -O Q.

C — IA O
O O i. 0
0 L. 0 0 U
49 49 u a
49 C 10 3
n o a. » IA
o e CD «
0) 3 0 U
o -o -o t. —
— c o. >
cat- 0
a o «--o
o> mq- o
L. C Q.—
o 0 o> a o
> u > c
en o 0 49
c u > 0 c
— o .c o
C— O 49 U

"o 'a t> ««- o
49 49 C — Z
c c a
O0 TJ
O •> 0 •
X IA U 10
e> 0 E —
C-C 3 DT3
49 H- t. cr c
a TJ 0 a
• u
* •«(- >
c o n TJ-
o o —
49— en -co
49 C 0 CM
x a.— o c
— o-o — - o
a. a > rn —
O. I. O 0 49
a a — -o n a.
— CO
10 3 "O — O
o o o • 	
-C — O) 1. 49 O
0)49 C 49 OLt.
3 L. 0 C 0 49
o a E o c
i. Q.J3 O — O
-C 3 O O
49 0 IA a L.
-C 49 C
1-1 49 - O C —
V) 49 O
»-C 49 U V)
c 49 c en -i:
o — 0 c i. c
— * I— o a
49 -O -P t- 49
Q.^ C C
0 O 3 0x-v49
49 O > — C
— SO. 0) 0
O — E - Q. E
t- O •— IA 49
49 O JC 10 Q
C IA-0 C • 0
O IA C IB iH t.
u a a 49^-49
6-2

-------
standards (52 FR 3748) are in effect.  Control  options 1 through 5
represent the potential "controlled" cases.  Data are presented for these
seven scenarios to allow comparison of the impacts of the control options
to current and to 1987 proposed standards on TSDF organic air emissions
nationwide.
     Chapter 3.0 of this document, "Industry Description and Air Emis-
sions," provides nationwide estimates of uncontrolled emissions by TSDF
management process.  Nationwide emissions were computed using the computer-
ized Source Assessment Model (SAM) by first identifying all process source
categories listed in the Industry Profile  (described in Appendix D.2.1).
Once these categories were identified, their emissions were calculated by
multiplying the organic quantity of each waste stream by an emission factor
specific to the particular management process and the wastes being
processed (see Appendix D, Section D.2.4.1).  Emissions per process per
TSDF then were summed to yield a nationwide uncontrolled emission estimate.
     To calculate the quantity of emissions reduced by applying organic
emission controls, the control technologies described in.Chapter 4.0 were
applied to the appropriate waste management processes (source category) as
required by one of five control options.   Control options  1-5 apply to
wastes containing organics at concentrations greater than  the action level
associated with the option.  They entail covers and control devices for
tanks  (including waste fixation) and impoundments, submerged loading of
drums, and covers for dumpsters.  For covered storage and  quiescent treat-
ment tanks, venting to a control device is required only if the vapor
pressure of the waste in the tank exceeds  10.3 kPa (1.5 psi) for control
options 1, 2, 4, and 5.  No control devices are applied to covered storage
and quiescent treatment tanks for control  option 3.
     The magnitude of nationwide organic emissions associated with each
option was calculated using the SAM.  In short, this consisted of adjusting
the uncontrolled and baseline emissions by the control efficiency of the
control technology required under each particular option,  for each TSDF
process stream at each facility nationwide.  Summation of  results provides
an estimate of emissions per control option.  Table 6-2 presents the
nationwide results by emission source resulting from implementation of.each
                                    6-3

-------


*
U)
§
M
\~

£j

o
£
§
O
cc
p
It,

Q
<
•»
UJ
^g
M
&j
co
a

i
i
u
ZZ
5

UJ
ce
o
u.
a
^^
rH
(/>
V)
3
1
a
M
gK

O
M
1"*
2?
t
CM
*~



L>
^ to
o
2

CO
S)
*"*
f ^f
n
c
o
4>
O

— CO
o
t_
45
u

I_
0 CM
•
C
o
°n *"*
a
il
JO
• I.
0 «1 >»
c c <;
.- O CD
— ~ a
0 .i^
4> n
c nco
O ••* tS)
U g tH






X
t_
09
•
U
e
u
r_
w





o
^H




CO
CO





to
CM



CO

to

T
CO







S)
tH
CO





61
CO

4?




0|
0
u
M 4>
•St.
• O
:&
§2
n 4>
0^
I





LO
OJ





5





CM
03





?


CO
*






TH
CM





5)
tH
CM

•JJ
« C



0
0
C L.
3 43
O
1°
45 C9
i?
83
0 n
•— ^M^
a





tH
CO





to
CM





CO
CM





CO
CM


CO
CM






S)
T





•*•





M
Jt
C.
4>
-quiescent
i





CM
TH




to
»-•



to

*



UJ

*

*
^f







*





It


1
•o
c
3
O
a.
e
-quiescent
ants
i




o>
^«





o>
^



^

"••



^f

*""

*
^







S





to
00









•o
n
t_
0
c
a
4>
0
o





0>
lH





0>
lH





TH
tH





TH
tH


TH
TH






S)
00
TH




lH
CM





45

*C
3
ta fixation
n
£





S)
00
TH




S)
tH




S)
CO
tH




S


ex
CD






§
00





i
03









Subtotal0




















































er sources
-C
4>
O



co
5> •*
SI CO




CO

SI co


CO
S) it-

si co


co
S> 00

si co
co
si oo
si m




CO
SI lH

SI CM




CO
tH
IS IS
•««•









vt t-
0  c
a a
3: _J
TJ
0
3
co c
TH •» SI
TH SI S> 1 to SI c
1 00 O
tH U


CO
tH •» 51
TH Q Q 1 1O SI
rH

co
tH •» CO

tH IS SI 1 to 6}
i *r


co


tH S) S) 1 UJ S
lH
CO

tH SI S» 1 10 CO
1 CD



CM
TH If f*"

tH S) Sr 1 CO SI
8




co co
CO •»
si co si t St SI
f- 1 TH S
TH
rt
to


..
•— > O
j: w
4> j£ ~n
CD c a c
CO 00 0
O E — —
— 43 n 45
4> a 43 45 C O
90 C 0 _l
!_!_.- 0 4> < 0)
0 49 W £ -0 1- 0
C — 0. 3 O 4»
.-,-.- W _ 0
C w Q. cr
M _l CO til 0
0
(O
6-4

-------





























^•^
"§
3
c

43
C
o
u

CM
1


Ul

m
I-








































































.
^.
^3
._
•_

U
19
«#-

_
IB
M
0
Q.
M

-Q
•o
C
a

!t
0
O)
a
L
o
49
0

49*
C

«5
^B|
t.



u_

l~
1
Q
M
0
01
3
a
U 01
0 0
-O U
t.
X 3
— O
49 01
C
0 49
•0 o
c a
|1
•O

•o 3e
0
* 43
0 IB
— *"
> 49

t- 01
O C
o
-o —
801
01


0 0
Q
0
49 U
c-o
0
-a t-

3 L.
O O
JZ
01 IA
C
X O

O 01
09  o •
0 E
J49 a
— L.
IB O 49
E I- M
— 49 C
49 C *
01 O O
UJ 0-0
IB





•_
IB
01
O
Q.
M

TJ

TJ
C

T3
C
IB
"•?

fg
0


49
c
1
a.

"3
cr
0

^v
c
IB

01
49
C
0


M
01

o
U


t_
o

v-/

0)

a
•o
c
a

IA

L. •
— 0
II O
01
•o —
0 a.
M
o c
Q.—
o
L. M
a. c
o

V) U
t.
JC 49
49 M

JQ
C «l •>
O C UJ

49 — -O O -C
II O, C L. 49
X Q. a 43
— II C C
•t. ... o —
rt E 0
C Q. C
49 C O. « 49
01 O 01
IB — s o a
*49S>49 *
O.UJ
CD O • C9 0


-O O «49
3 t. •* e«t-
— 49 00
O C ••> >
C 0 E 0
— u a « i.
^ Q. M 3
jc n
M • (9 C M
je M (9 « 0
C U UJ 49 t.
a 0 a
49 49 -43
01 CO C L.
«. a. 00
o E •- £ a.
<*- 3 E-P a
-o o. a >
0 a 0
01. L. 0
0 0 S 43.C
— t-  UJ 49
00) C «t-

0 CM* U*
— > 01 -
O O •« 0 UJ
L. O 01 —
49 O 3TJ
c -o — or c
O c c a
o a a -o
09C -
"O • 1- « ^
C M O
a E 9 -
=m- en CM
M u o a
c. -o t- «
0 E O tH

O O 0. 0) 0)
u c
O>5> "O O

•— •«• C !- 49
a-o a 0 a •
49 a jc > o^
C 0 49 0 —
0— O— 01
L. o a.
uj-o c t. t.
O 43 O 43 UJ
JC O9 9 U. C •
OS L. 0 O tH
3 0 L. O''-'
O E O> •
t-_o IA c a
JC 3 O9 O — Q.
49 IA C — -*
— c-o '
IH - c a 0 co
0) — O» 1. •
» 43 a L. — O
C C49 0 3 f<
O 0 c cr
— E 0 1- 9. M
43-O O O t- T3
0. C 0
0 3 M E M 0
O 0 Q.— O
— 0.43 0. X
0 E 01 00
L — as u
49 * 3 — -*
c-o s > c
o c o - 0 a
U 049 WO 49
o
^
•••
— 49
o c
U 0
49 U
C 1.
0 3
u u

0 0
JC U
H o

>t
• 0

C 49
"0 0
IB IA
O 3
— o
U '
|.8P

0 49
- O) t.
&a IB
U O.
a 0.0
t- 49 3
0 IAW
0) L. -
0 UJ
1- 43 CO
0 IA CM
49 a.
o) e -o
O, 3 C
E-o a
3
•OTI •»
« a CM

E oi
19 3 49
L. U t.
o-o a
49 0.
01 O
49 Q£
3 01 U
L. —
"DOS
t- ^
01 49^
0 C
•o o oi
3 U C
— o
o 	
C IB 49
— c a
o —
X— 3
L. 49 O>

O)^3 !•
ffl ™f5
•^ fll O)
IB C
O X—
— 49
0 a. M
u a—
t. a x
3 0
049
0) O X
C J3

n 0*0

c o —
— CO
a o t-
49—49
C43 C
o a. o
u o u
-Q
.
OJ
c
•o
c
3
o
^

*^"
o

0
01
3

o
i
01
0
3
a


w
qi
49
o
49
T3
c
a

a
49
o
49
ft
3
IA
0
JC
49

«.
a
3
o-
0

49
0
c
0)
0
o
-o

s
a
•p

 O
— c —
— — 4>

0
— 0 C —
49 JT 	
— 1 	 0)
TJ -0
-o c c
B • 8 —
VI JC
X C IA
— O fll 49
O.— 0 —
0.43 U 3
a o t_ oi
— 3 0
49 t. O U
O 49 01
C V) -O
0 C C
0 t. — 0
"O 0
— 49 01
M a u c
C M 0 O
o o o —
— O. M
49 01 0 M
Q.— (A —
O-O 3 E
IB 0
— -o o
O C 0 01
u a -o 0
49— 
C 01 01 •
0 0 C 0 01
O -C O t- O
49— 0.49
0 49 a 01
jc x a. 3 a
1- -O O M *
«l-
•«• a
CO M
•O CM O
0 -O Q.
43 a: c 01
• u. a —
I- U C -O
0 -0 C

— •*• -o — c
o 	 a
C t. 3 0 —
— 0 0 01
-o * a 0
X C J2 JC
— 31. 49
0 0 0

— "0 0H 0
49 49 t. I.
3 a a t-
o —
t. 3 49 IA 09
O) a c c
0 0.C O —
a '••P3i
X 01 U 3
49 — 0 — 0)
IB 49 49 t. 0
JC C 01 49 L. •
49 0 a 01 S)
t. t 0 C •
01 i. I- O UJ
030 —
43 0-0— 01 L.
«i 3 a oi 0
9 0 — 01—49
$ i- o o E a.
A C Q. 0 a
E — «> JC
o o) — t. u
L. 0 49-O O
4. U O 49 C
i. c -o a —
01 3 C t.
C O 01 IB 0~O
O 01 0— C 0
— 0 — C
0) 0 -0 < O —
oi oi a: c a
— 0 O O • 	
E JC — K O.
01- L. 0 x
a 0-c 0
0 C .C 43
TO • 0 43 0
3 01 O «- I.
— — IA o) o a
u o c<<-
C J. C — 01
— 49 O 49 49 O
c — c c —
oi o ei 0 3 t.
c o IA E o a
O — 0 U C
— c E — o 0
IA o 0 a a u
01 — E IA
— 01 -o — •
E oi 0 t. c

* 'i — *o > —
t. 0 O 0 01
O l_ 43 * W
49 01 49 — O —
a a c 3-c E
«. O9 O 01 0
0 O 0 -
C 49 C L. O 0
— 01 3 -OJC
u 3 a l-
c a 0 B)
— JC JC M C
x I- a o •
-00 — M
0 -O 49 C
__* . e 0.0
— O O 49 O —
o a a 49
U 43 43 t.— U
49 01 L. 0 O —
C 0 C I. 1-
O JC Q. 	 P 49
O 43-d O C W
J— 3 C O 0


«K
a
M
o
O.-D

IB O
si
.a L.

B U
{S •«>
B C
a
0 a
L. t.
IB O
0) 0
C "****
.2-4!
49 a
a.—
O 0

V— "
O I-
i. 0
c
0 49
u c


C 49
a a
0
0 1-
C 49
— 0
— 1.
8 a
IB 0
J3 U
•^
0 3
j= cr
490
L
o o
<*. 49

M -O
C 0
O E

'« 01
M 01
•_ (0
E
00
49 a
i M
E c
49 O •
a— 49
0 49 C
*^l
L. 49
-o 49 a
C M 0
IB 0 (-
_l t. 49
JC
9
•o
c
3

•o
0

—
o
t_
49
c
o
u

0
u
a
X
0
49
0
01
3
a
o
0


IA
*M*
• 
0
x t-

0.0;
a o
on
49
O U5
C CO
CM
o
•o-o
c
01 IB
c
o ^
38
o.
O 49
u.
— a
00.
49 09
c c
o •—
U 49
ei

JC X
1- 0
••"



49
o
c

o
•o

01
0
3
^
19


a
43
3
0
01
0

1"™


•
"O
o
01
«— >
J>
0

OJ
c
—
0
-0
X

49
c
0
u
t.
3
o
0
1.
a
01
V
a •
9 M

IB
49 0
ffl
E 49
o. c
— 5
3 E
o- a.
9 —

t. or
O 0

L.
M O
l-t-
9
-15
3 —
c a
c
O 0
*IA 3

— "3
,§.E
•— >
6-5

-------
             control  option by source category.   Because the specific  design  and
             operating characteristics of each waste management process  are not widely
             available,  nationwide distributions of process  design  and operating
             parameters  were used in estimating  TSDF emissions.  Therefore, it is
             appropriate that nationwide TSDF emissions  and  impacts are  used  in the
             comparison  of the various control options.   As  noted in Chapter  3.0,  the
             estimation  of TSDF emissions in  this document  involved the  use of the TSDF
             air emission models as presented in the March  1987 draft  of the  air emis-
             sion models report rather than the  December 1987  version  of the  report.
                  Comments have been received providing  additional  information on  the
             concentration of organics in biologically active  treatment  processes  and
             the aeration parameters used for the model  units.1  Proposed revisions to
             the aerated units and the biodegradation model  were evaluated  in a sensi-
             tivity analysis  to determine the effect on  the  nationwide impacts presented
             in  this  document.2  The results  of  the analysis showed that the  combined
             effects  of  the proposed changes  had only a  minor  effect (less  than 5  per-
             cent) on  nationwide impacts.  Consequently,  the impacts presented for
             emissions and incidence,  although based on  the  original biodegradation
             model and material  balance in Appendix C, Equation C-5, would  not change
             significantly with the revisions that  were  proposed to improve the modeling
             approach.
                  Nationwide  uncontrolled  organic air emissions were estimated at  about
             1.7  million  Mg/yr;  baseline emissions  were  1.8  million Mg/yr.  Quiescent
             tanks used  for storage or treatment are the  largest uncontrolled emitters
             nationwide  under these two scenarios.   Land  treatment  sources  have zero
             emissions for the  baseline and controlled cases because the land disposal
             restrictions  will  require pretreatment to remove  volatile organics prior to
             land treatment.   The  control options do not  apply.to drum storage because
             this source  is controlled by existing  regulations  (CFR Parts 264 and  265,
             Subpart I).   Similarly, wastepiles  and landfills  are not  controlled under
             the options  because they  are controlled  by the  land disposal restrictions.
                 Emission  reductions  from baseline for the  five control  options range
             from 1.6 million Mg/yr  (control  option  5) to 1.7 million  Mg/yr (control
             option 1).  Control options for  quiescent tanks yield  the highest emission
             reductions.   Some  sources  such as landfill and  incineration  processes show
_
                                                6-6

-------
an increase in emissions when a control option is applied.  These increases
occur because (1) emissions are suppressed from upstream controlled sources
(i.e., the waste stream retains the organics that would have been emitted
previously, which results in an increase in organics at the source of
interest), and (2) when controls are applied, new emission sources are
created such as pumps and valves (i.e., equipment leaks).
6.2  HUMAN HEALTH RISKS
     Health risks posed by exposure to TSDF organic air emissions are
presented in this section in three forms:  annual cancer incidence
(incidents per year nationwide resulting from exposure to TSDF organic air
emissions), maximum lifetime risk (the highest risk of contracting cancer
that any individual could have from exposure to TSDF emissions), and
noncancer health effects (from acute and chronic exposures to noncarcino-
genic chemical emissions from TSDF).  Annual cancer incidence and maximum
lifetime risk are used as an index to quantify health impacts for seven
cases:  (1) uncontrolled organic air emissions, (2) baseline air emissions,
and (3) controlled emissions under the five options.
     Detailed discussion on the development of the health effects data
presented here are found in Appendixes E and J.  In general, the methodol-
ogy consists of four major components:  estimation of the annual average
concentration patterns of TSDF organic air emissions in the region sur-
rounding each facility, estimation of the population associated with each
computed concentration, estimation of exposures computed by summing the
products of the concentrations and associated populations, and, finally,
estimation of annual incidence and maximum lifetime risk, which are
obtained from exposure and TSDF emission potency data.
6.2.1  Annual Cancer Incidence
     For the estimates of TSDF incidence, the Human Exposure Model (HEM),
which uses a basic EPA dispersion algorithm, was used to generate organic
emission concentration patterns.  The TSDF Industry Profile (see Appendix
D.2.1) was accessed to identify facility locations for population pattern
estimation within the HEM using 1980 census population distributions.  The
HEM was run for each TSDF using a fixed unit risk factor and a facility
organic emission rate; as such, the HEM site-specific incidence results can
                                    6-7

-------
 be adjusted  by  the  annual  facility  emissions generated  from the SAM and the
 appropriate  TSDF  unit  risk factor to give  facility-specific estimates for
 the control  option  under consideration.  A unique unit  risk factor was
 derived  for  each  option based  on the emissions of specific carcinogens
 under that option (see Appendix E).  The incidence  results therefore
 reflect  the  level and  composition of emissions resulting from a particular
 emission scenario or control option.
      As  shown in  Table 6-3,  incidence estimates  indicate that an uncon-
 trolled  TSDF industry  would  lead to 130 cancer incidents per year
 nationwide;  the baseline TSDF  industry case would lead  to 140 incidents.
 Control  options 1 through  5  reduce the estimated number of cancer
 incidences by 89  to 95 percent from 140 in  the baseline case to a range of
 6.4 to 16 per year.
 6.2.2  Maximum  Lifetime Risk
     Maximum lifetime  risk  (MLR) represents "individual" risk as opposed to
 the "aggregate" risk in the  total nationwide cancer incidence and is
 intended to  reflect the Nation's most exposed individual's chance of
 getting  cancer  if exposed  continuously for  70 years to  the highest annual
 average  ambient concentration around a TSDF.  As such,  MLR reflects the
 highest  risk that any  person would have from exposure to TSDF emissions.
 MLR  is calculated as a function of ambient  organic concentration and the
 composite unit  risk factor for TSDF organic emissions.  For TSDF MLR
 estimates, the  Industrial Source Complex Long-Term Model (ISCLT), a state-
 of-the-art air  quality dispersion model, was used to generate the maximum
 annual average  ambient organic concentration estimates  (see Appendix J for
 a description of the model).  In order to provide a more comprehensive
 analysis of maximum ambient concentrations, two TSDF were selected for
 detailed, rigorous analysis in making MLR estimates.  The two facilities
were selected on the basis of their estimated emissions and the TSDF
management processes utilized at the facilities.  The design and operating
parameters and wastes managed at these two facilities were used in conjunc-
tion with the local meteorological  conditions (standard climatological
frequency of occurrence summaries)  to estimate dispersion of emissions from
each source at each facility on an annual  basis.  Multiplying the maximum
annual average ambient concentration by the composite unit risk factor
                                    6-8

-------




jo

a

ec.
8
1
3

Ul
f£
g

>_
ffi

S
O x-v
HI 1.
OT 0
M >
UJ 0)
0
U. U
a c
J2J
2 'G
O C
a: M

^
Ul 0
u u
Ul 0
o o
HI
u t-
5°
Q£ S)
UJ n°
^J E
Z 3
O "- '
UJ
S
HI
CO
CO
UJ
GO








•
•
B
i.

49
*fr*
a
0
u
c
0
•o

u
B_
1.
8
c
a
u









































TJ
in
c
o
•_JJ
a
o
_
o
t-
c
o
0










(

0
U '
c
0 • 0
-o

u



03-
o ~v
c
a •<


















UJ



^.





co




CM




^




",

: c
- o
) 'in
1 0)

»'"i



9
B
- e>
- c
o o
L —
» w

5 —
U E
§ «





>v
L.
O
!
u
0
o
3
o
in



if CD UJ U5 00
OOSCOSOOOO CMS S CO
1-1 co ^iHS^CD SSSSSISCO
1-t 1 f-l


i-l 0> CO CO CO UJ
cor»u>r~o>S cos S •»

1-1 uj CISSOM*- sssssis^;
1-1 1 1-1


S CM S S UJ UJ S
CM CM f^ S S S CO S l& S) Q) C9 1 ^3 GD
t


CM UJ CO UJ UJ CO (O h-
t-. -*r IH co oo en v cos s v oo
S i-« CMSSSCO SSSSSISCO
1


00 UJ V •V UJ CO CO f-
••r co s co oo oj o> cos s - iH S»-lSCOS CO

1-4 OJ OO^h-SS SCMSSSIMS
00 CM CO 1 CO
1-4 i-l



in
x^ x-v C
-p -P 0
C C i
J-P O T)
c E c w
043 n 3 -P
ra E • -x o — — >
0-00CO.C — W
i. c i. a E 3 4>JC
0) .P 3 -P -P — -C C 10
^0 C49 O— CBO> OE — —
2OEOCC — a 0 B> TO •- -P R>
— 0004>-P O 0 » -P 0 4>-P<«-
0 0 u o «> <» o c — — a 0 c o _l
4»O)-PO)«>«I«-X4» 3 — — LI. 0-P<
cacti 000 — ja DO.— 04>o>£jil-
01.01..-— C«l-3 M0<»-C — O. 3 O
OOOO33-- CO 43-O — -O — — COH-
Gk-PM490rCrA0 L. 0> C U C *— 3
0CD0NI i .p -P 0(g(eccocxcr
.--.:•.-•.> C C C M J=S-IH4_ICOUJ
3 3 O O O « -P
or or z z <-> s o
?
3
c
4>
e
o
u



















































6-9

-------
-o


 c

4>

 O
 O
o
         £
          M

          a
          n
         1
          |

          t.


          n


         4?



         I
          u
         u.
       C —"O
 x n — 49 c
—  O     d  T
49  O> C  t —
 C  C— 49
 O  d     CO
 u.c  o  o 49
 t.  u  n  u
 3     act.
 u  o  o  o o
   .c  i-  u —
 O 49  U    L.
 u     c  u a

    o'  "c n
 x o  o  d o
 o — .c  o> o
-C <•- 49  U t-
49  O     03
    I-  -   O
 O     C  t- IA
 IA  O  O  O
 3  l> — JC C
 d  C 49  CD—
 O  O — —
 OTJ-O-n 49
JQ.-TJ    t.
    O  d  E O
 M  C     O U
 C —  C  I.
 O    W«l- O

49  o     «
 a    •  c -o
 O  IA^-x O O
    O UJ — —
— 49     0» —
 o  d  x  IA a

£ J=5-i &
 C 49  C  O
 O  IA  O    IA
 u  o  a c —
       a— o
 o  c <    t-
-C —     O 49
49     OWC
    n  o  d o
 t.  o  n  o o
 o  co^ t-
-o  c     u c
 C  d  C  C O
 3.C  O ——
    O—    IA
-a    49 49 IA
 O  e  a-c o
                                                                    o	a
                                                                    u    o n 3
                                                                   49  • L.    01
                                                                    C (A 49 d
                                                                    o E c    o
                                                                    O d O 049
                                                                      i- u e)
                                                                   49 09  — O
                                                                    O O-C d 3
                                                                    c t. u   -o
                                                                      O O— B>
                                                                    «43q-«l- d
                                                                    O d  ,  O *
                                                                    o— t.  t.
                                                                    t. 3 o    -a
                                                                    3 CO 43  (A O
                                                                    o o o	
                                                                    (A t. d	
                                                                    O L.
                                                                    IA O JC "O -O
                                                                    Of IA C C
                                                                   jr 4> — d d
                                                                   I- O I.	
                                                                   O9
      849 49 E
       O  IA O
-o  o  c  o t.
 3 j:     t-«t-
— I-  (A
 U     O— 00
 C     O  d C
—   • -O  IA —
    (A     O 49
 »—  o  a—
 C  O —  Bl 3
 O  U  t. — IA
— 49  d -O O
 _d o

    o  c    '«  •
 t. —  o < MS

49  IA *IA 
 d —  IA a: o

 o  o 'E  o L. o
 C     Of O 49
—  n    49 49 a
 U  d~O    d d
 C  09 O  CO I- .C
      —  c ou
   49 —— C
-o  n  o 49 — c
 O  3  1.  C O —
—  d 49  O C
— -C  C  E — T>
 O  X  O  O    O
 t.  o  u— o c
49     c  Q.-C —
 C JC  3  E 49 d
 O  O    —   —
 u  d  o    t. a
 C 49 f  I-  O«f- O
                                                                                                                o
                                                                                                               •o
                                                                                                               _3

                                                                                                                u
                                                                                                                c
                                                                                                               49
                                                                                                               o
                                                                                                               o
                                                                                                               d
                                                                                                               49
                                                                                                               O
                                                                                                               49
                                                                                                               •o
                                                                                                               O
                                                                                                               IA
                                                                                                               O
                                                                                                               49


                                                                                                               O

                                                                                                               t-
                                                                                                               3
                                                                                                               U

                                                                                                               O

                                                                                                               d
                                                                                                               o
                                                                                                               49
                                                                                                               C
                                  O 49 49
                                  U    C
                                  COO
                                  d CA E
                                  U 3 49
                                     CD d
                                  O U O
                                  -C O L.
                                  (-.0 49
 IA  O

||

 e'H
 3  cr
 c  o

 O  t.
 u  o
 C If.
 o
-O  o

"o —
 C  d
M  >
                                                                          6-10

-------
yields the maximum risk, given that someone is predicted to reside at that
location.  The unit risks from the various individual dispersed carcinogens
are represented by a composite unit risk factor derived for each option for
TSDF organic emissions.  Pertinent information on the selected TSDF and
unit risks is presented in Appendix J and Appendix E, respectively.
     The results of the MLR calculations, shown in Table 6-4, indicate that
the probability of contracting cancer is 2 x 10"2 for the baseline TSDF
industry.  For control options 1 through 5, these risks range from 5 x 10~4
to 9 x 10~4.  For all options, aerated units are the major sources
contributing to the maximum ambient air concentrations associated with the
MLR values.
6.2.3  Noncancer Health Effects Assessment—Acute and Chronic Exposures
     A screening analysis of the potential adverse noncancer health effects
associated with acute and chronic exposure to individual waste constituents
emitted from the two selected TSDF was based on a comparison of relevant
health data to the highest short-term (i.e., 15-min, 1-h, 3-h, and 24-h) or
long-term  (i.e., annual) modeled ambient concentrations for chemicals at
each facility (see Appendix E).  Modeled concentrations were estimated from
the Industrial Source Complex-Short Term (ISCST) Model.  Detailed informa-
tion on this model and on modeled ambient concentrations of constituents at
each facility is provided in Appendix J.
     Results of this analysis indicate that adverse noncancer health
effects are unlikely to be associated with acute or chronic exposure to the
given ambient concentrations of individual chemicals at these two TSDF.
Modeled short-term and long-term ambient concentrations were in most cases
at least three orders of magnitude below health effects levels of concern.
It should  be noted that the health data base for many chemicals was
limited, particularly for short-term exposures.  The conclusions reached in
this analysis should be considered in the context of the limitations of the
health data, the uncertainties associated with the characterization of
wastes at  the two facilities, and the assumptions used  in estimating
emissions, ambient concentrations, and the potential for human exposure.
                                   6-11

-------
        TABLE 6-4.  MAXIMUM  LIFETIME RISKS FROM
                    TSDF  EMISSIONS9
Control scenario
Uncontrolled
Baseline
Option 1
Option 2
Option 3
Option 4
Option 5
Maximum
concentration,
/jg/m3
1,700
1,700
43
43
47
60
81
Maximum risk*3
2 x lO-2
2 x ID'2
5 x 10-4
5 x 10-4
5 x ID'4
8 x ID'4
9 x ID'4
aThis table shows the cancer risk of the individual in
 the United States most exposed to TSDF emissions over a
 70-year period.  Risk is presented for seven scenarios,
 which are described in detail in Chapter 5.0.
 Development of risk data is presented in Appendixes E
 and J.

bBased on the composite risk factors derived for each
 scenario as described in Appendix E.
                         6-12

-------
6.3  OTHER ENVIRONMENTAL IMPACTS
     The types of environmental impacts that potentially may result from
the operation of control devices used to reduce TSDF organic air emissions
were discussed in Chapter 4.0.  Estimates of the magnitude of the secondary
air and cross-media impacts associated with the different control options
were prepared using an approach that applied energy conversion factors, air
emission factors, and wastewater and solid waste generation rates to the
results of the Source Assessment Model (SAM) control option analyses.
     The secondary air and cross-media impact results are sensitive to the
control device operating conditions used at TSDF (e.g., electricity source,
type of fuel burned to produce steam, spent activated carbon management
practices).  To account for this sensitivity, a range of secondary air and
cross-media impacts estimates was computed for each control option by
defining two sets of TSDF control device operating conditions that provide
an upper boundary estimate and a lower boundary estimate.  This approach
allows a range of values to be computed that spans the conditions most
likely to occur at TSDF on a nationwide average basis.  The two sets of
TSDF control device operating conditions selected are summarized in Table
6-5.
     A nine-step procedure was followed to estimate nationwide annual  air
emission, wastewater, solid waste, and energy impacts produced by the
operation of the control devices selected for each control option.  The
procedure is outlined below:
          Define the TSDF control device operating conditions.
1.
2.
     4.
     5.
Develop TSDF source category operation factors relating
specific control device operating requirements (e.g., elec-
tricity demand, steam demand, activated carbon requirements)
to the amount of hazardous waste managed.
Select energy conversion factors for electricity generation
by fossil fuel-fired utility power plants and process steam
production by industrial boilers.
Select air pollutant emission factors for utility boilers,
industrial boilers, and hazardous waste incinerators.
Select wastewater and solid waste generation rate factors
for utility power plants, carbon regeneration units, and
hazardous waste incinerators.
                                   6-13

-------
  TABLE 6-5.  TSDF CONTROL DEVICE OPERATING CONDITIONS SELECTED FOR
           SECONDARY AIR AND CROSS-MEDIA IMPACT ESTIMATES
  TSDF control device
  operating condition
      Lower
     boundary
     Upper
    boundary
Electricity

  Electicity source

  Electric utility
    power plant mix
Electric utility

50% coal
25% natural gas
25% noncombustion
Electric utility

   100% coal
Process steam

  Process steam source


  Steam boiler fuel
Onsite industrial
   boiler

 100% natural gas
Onsite industrial
   boiler

  100% fuel oil
Carbon adsorption units

  Fixed-bed carbon unit
    regeneration yield

  Spent carbon canister
    management practice
       903
 100% regenerated
  with 90% yield
     803
   100% direct
landfill disposal
                                6-14

-------
     6.   Obtain SAM results for each control  option listing annual
          nationwide hazardous waste throughput (megagrams of waste
          per year) by TSDF source category.
     7.   Multiply control device operation factors times individual
          TSDF source category throughput to obtain annual electric-
          ity, steam, and carbon demand for each TSDF source category.
     8.   Add the individual source category demand values to obtain
          the total nationwide annual electricity, steam, and carbon
          demand for each control option.
     9.   Multiply the total annual electricity, steam, and carbon
          demand values by the appropriate energy conversion factors,
          air emission factors, and wastewater and solid waste genera-
          tion rate factors to obtain nationwide annual secondary air
          and cross-media impacts.
     Control device operation factors were developed for each TSDF source
category using the control cost estimates presented in Appendix H.  As  part
of these cost estimates, annual control device electricity, steam, and
carbon consumption were computed to determine capital and annual control
costs for individual TSDF model units defined for each TSDF source cate-
gory.  Each operation factor was calculated by dividing the control  device
annual consumption value by the annual hazardous waste throughput defined
for the model unit.
     Energy conversion factors were selected based on engineering judgment
to be consistent with typical electric utility power generation and indus-
trial process steam production practices.  Fuel property and air emission
factor values were selected from the EPA document Compilation of Air Pol-
lutant Emission Factors (AP-42).3  Wastewater and solid waste generation
rates were computed for the defined TSDF control device operations and  fuel
property values.  The specific values used for the secondary air and cross.r
media impacts calculations are listed in Appendix K.
     Secondary air and cross-media impacts were estimated for each control
option using the TSDF source category nationwide annual hazardous waste
throughput values estimated by the SAM analyses.  The nationwide secondary
air pollutant emission impacts, wastewater discharge impacts, solid waste
disposal impacts, and energy impact for the five control options are
presented in Table 6-6.
                                   6-15

-------

to
c
o
49
Q.
0

1
p
M
UJ T
S3 §

ft 49
M O

^
w

UJ

to
O CO
OS
U C
m 6
Q "» 2
_ 0 0
a: 3
M O
< cc
>• f
o«

S S2
So w
UJ M
to 1- c
CL 0
_) O •—
< 49

^C ^™
%£
U) O
0 U

is
o u.
M
1™ *H
*f
Z c
0
5 *
>- o

S
3
ZD



•
CO
t


UJ

f 3
u
1
11








V

1
CO



i


S







51
CO

1
r-







S
«H

1

IS
tH







Si
CO
fH

1
s
IH











s-* O
t, C£

i $
X
1) O
c c
O 0
*"* Cl
V) C
••" o
§-n
l_

u u
•»•
<

§ i
CO r-

1 1
i §
CM fH


gfQ
«
CO .H
1 I

§ i
•*• »H






§
1 T.
•^ ^t

i t
§ §
10 CM






i §
10 f-
f-T CM"

i i

i i
SI T

fH




§ i
f- CM
«, 4,
tH (0

i i
O O
SI IS
CM ••»•

fH







^•^
X
o ^
Z X
•** o
B •*-*
O
TJ n

x -o
o —
X
c o
o
9 =•
t* *T™
43 _.
— 3
z co



S

•
fH



S
1

SI
fH







SI
CO

t
g







§
fH

1

T







SI
fH
fH

1
^-













t.
O
49
49
a

|
—
u
43
L.
a
Q_


























































^•^
L.
>^
•v.
co
E


c
j

0
L.
4?
a
*
0

n
0
£&
1
fH
fH

1
§
O

to
i
fH
,

i

CO




g
CO
fH

1
I

oT




1
10~


1

i

CM
CM



1

fin.
^

1
i


CO
CM













49
a

a.
u
0
S
o
a.


§
s
r«.

i



CO
SI
SI
SI
fH
,

SI

O)




§
SI
oT

1
I

oT




g
eo"
CM

1

i

^
CM



SI

d>
m

i
§
SI

10
CM









C.
S
a
L.
c
0
o>
0
i.
c
o
J3
t.
a
0


i
>«•

•



CM
1
CO
1

1

co"




SI
"^
h-

1
i

CO




g
CO
fH

1

i

CO




i
•,
r-
fH

1
St


o>











^ JO
^^ II)
at m

<^r 49
o a
49 —
0) Q.
a
f i.
0
•o *
— o
— a.
o
CO
SI
SI
SI
CO

i
1
O

CO
SI
1
oT


I

10




SI
fH
fH

1
SI

co"




SI
eo"
CM

1

i

CO
T-l



i
M
CO
CM

1
1
(S

•^~
fH










JB
O
ra
•a

u
L.
0
^3

L.
U
(O


SI
CM"

i
SI
SI



i
CM"
t

s






§
CM
fH

1
SI
SI
CO







,
u>

1

SI
SI

CM




i
•f.
<^>
TH

1



CO






c
o
jQ
t.
a
u
•o
4?
IB
49
U
a
49
C
0
Q.



SI
S)
CO
CM"

i
St
SI
10

CM"
§
CM
1

§
to

co




i
to
LO

1
SI
SI
fH

10



Si
SI
SI
fH
fH

|

SI
SI

s
«H



§
SI

CO
fH

1



CM
fH









t_
^
—)

U
ra
a.
E
^^
en
i.
0
c
m

u.
H~

c
a

• to
.C VI
DO 0
3 U
O *~
1. >
-C 0
49 T)
fH —
O
0) i.
C 49
0 C.
3 8
o.
o u.
a
— CO
0 1-
t.
^ 0
C 49
o a
u t-
0
t- a.
o o
o
II) 49
49
— "D
3 0
II) t-
2 •-
cr
tn 0
— <-
vt

to •—
c • o
a 10 —
l t.
< 0 0
CO— —
v-'.O 0
a
— t— t-
0 o
•D C
o— c
S O
•o —
49 0 49
c 49 re
gut t-
.— 9
n— c
in 0
0 II) O)
in c
ID O O
•< •- 49
49
0— 0
u c -o
3 O
O U 49
CO O
en a
c c a.
o— E
49 •—
^ CO
01. 49
II) 0 C
ma. a
jB 0 —
CL
0 O
O) O t-
C— 0
a > s
u o o
"O Q.
0.
49 — >,
a o 49

• ^ 49 «•>
49 C —
no 49
UJ 0 3
a j>
6-16

-------
     To provide a sense of the magnitude of the nationwide TSDF control

device secondary air and cross-media impacts, the values presented in Table

6-6 can be compared to the impacts produced by a single coal-fired utility

power plant.  Recognizing that the TSDF control device impacts would not

all occur at a single location, the order-of-magnitude of the nationwide

control options 1 through 5 impacts is comparable to the air emission,

wastewater, and solid waste impacts associated with a new 100-MW utility

power plant burning a high-sulfur coal.

6.4  REFERENCES
1.   Chemical Manufacturers Association.  Comments of the Chemical
     Manufacturers Association on the Environmental Protection Agency
     Document "Hazardous Waste TSDF - Background Information for Proposed
     RCRA Air Emission Standards - Volumes I and II."  Washington, D.C.
     July 11, 1988.  105 p.

2.   Memorandum from Coy, D., RTI, to Docket.  January 1989.  Investigation
     of and Recommendations for Revisions to Aerated Model Unit Parameters
     Used in the Source Assessment Model.

3.   U.S. Environmental Protection Agency.  Compilation of Air Pollutant
     Emission Factors, 4th edition, AP-42.  Office of Air Quality Planning
     and Standards, Research Triangle Park, NC. September 1985.
                                     6-17

-------

-------
                     7.0  COSTS OF THE CONTROL OPTIONS

     The purpose of this chapter is to present the methodology used to
estimate nationwide costs of adopting each of the five control options
described in Chapter 5.0 as the basis for regulation of air emissions, from.
hazardous waste treatment, storage, and disposal facilities (TSDF).  Esti-
mated nationwide total capital investment (TCI; i.e., equipment purchase
and direct and indirect installation costs)  and total annual costs (TAC;
i.e., costs of operating control technologies minus any energy or materials
credits) are provided in a subsequent section of this chapter.  In addi-
tion, the cost per unit of waste throughput for the control technologies
identified in Chapter 5.0 as part of the control options is discussed and
listed, and a general explanation of the methodology used to derive those
unit costs is presented in this chapter.  Supporting data are provided in
Appendix H to this document, and other references to cost information are
listed in that appendix.
     Development of costs requires the presumption of a baseline level of
emissions and emission control from which the control costs can be calcu-
lated.  The baseline used for this effort is described in Chapter 5.0,
Section 5.1, of this document.  Costs to implement the control options are
provided to permit a comparison of the resources that would be expended to
reduce air emissions from TSDF using different combinations of controls and
sources.
7.1  CONTROL COSTS DEVELOPMENT
     Estimation of the nationwide costs of adopting a control option begins
with estimation of the control costs for individual waste management units
within a TSDF.  Ideally,  information about the design and operating charac-
teristics (such as surface area and retention time for impoundments) of
each waste management unit would be available to permit accurate estimates
                                    7-1

-------
of control costs for that unit.  Information at that level of detail is not
available for each unit at each facility; generally, only waste throughput
is known.  For this reason, model units were developed.  Rationale for the
development of model units is given in Chapter 3.0, Section 3.2.1 (as
relates to emission estimation) and Section C.2.  Control cost estimates
were developed for each of the model units (results are shown in Section
C.2.3).  The methodology for developing control costs for the model  units
is described partially in Section 7.1.1 and in detail in Appendix H.
     To obtain nationwide costs from model unit costs requires a method of
assigning a model unit cost to each waste management unit in each facility
and then computing the sum.  Given that only TSDF waste management unit
throughput is known, the assignment of one of the defined model units to
represent each TSDF waste management unit is not possible.  Therefore, a
weighted average model unit control cost—in essence, "national average
model unit" control cost—was derived for each control applied to each TSDF
waste management unit.  These control costs,  divided by the model unit
throughput, provide cost factors that are used to generate control cost
estimates for each TSDF facility.  The discussions of weighted average
model unit control costs and control costs as a function of throughput are
given in Sections 7.1.2.2 and 7.1.2.1, respectively.
7.1.1  Methodology for Model Units
     To estimate the nationwide cost impacts of implementing the five
control options presented in Chapter 5.0, the estimated total capital
investment and total annual costs were developed for each of the various
control technologies applied in the control options.  (A general discussion
of these control technologies is contained in Chapter 4.0.)  The control
options describe the control technology for each source category in general
terms, such as cover and vent to control device. • The specific control
technologies assumed to be applied to each source category for each option
are defined in Chapter 5.0, Section 5.4.
     A standardized cost estimating approach was developed for add-on and
suppression-type control devices based on an EPA cost manual 1 and a series
of articles by Vatavuk and Neveril.2'7  These sources identified the total
capital investment, annual operating costs (costs of operating control
                                    7-2

-------
technologies minus capital recovery and energy credits), and the total
annual costs (i.e., annualized costs) as the key elements of a cost
estimate.
     For each control technology applied in a control option, a detailed
cost estimate was developed.  The detailed cost estimate consisted of three
standard cost tables.  The first of the three cost tables lists the major
equipment items associated with the control technology.  The second table
lists any auxiliary equipment required, instrumentation, sales tax and
freight, plus direct and  indirect installation charges.  These first two
tables are used to calculate total capital investment.  The third table
lists the direct operating costs, indirect operating costs, and energy
credits  used to calculate total annual costs.  Examples of these three
tables are presented in Appendix H.
      The purchase  cost, material of construction, and size of each major
equipment item were obtained from vendor data, engineering handbooks, the
literature,  and currently operating commercial facilities.   (Such sources
are  referenced in  Appendix H.)  The sum of the costs for the major equip-
ment items  is equal to the base equipment cost  (BEC).
      Using  the base equipment cost, the purchased equipment  cost  (PEC)  for
the  control  technology is computed.   Direct  and  indirect installation
charges  for each  control  technology  are factored directly  from  the
purchased equipment cost.  For this  analysis,  the direct and  indirect
installation factors are  based on  information  obtained  from  vendors,  other
cost estimates,  data summarized  in References  2  through 7,  and  engineering
judgment based on typical TSDF wastes and  operating  practices.   The  costs
for  site preparation and  buildings were based  on vendor information  and
construction cost reference  sources.8  The  sum of the  purchased equipment
cost, direct installation charges, and indirect  installation charges are
equal to the total capital  investment (TCI).
      The sum of  direct  and  indirect  operating  expenses  less  capital  recov-
ery  and energy  credits  is equal  to the annual  operating costs.   The  total
 annual  cost is  equal  to  the direct plus  indirect operating costs less any
energy credits.
                                     7-3

-------
      To illustrate this cost approach for add-on  control  devices,
 Appendix H gives detailed cost analyses for control  technologies  used  in
 the control  option definitions in Chapter 5.0.  Appendix  H  provides  the
 rationale for the design, costing,  and material and  energy  balances  for
 TSDF control  options.   In addition,  Appendix H  provides sample  calculations
 and other details of how each control was costed.
 7.1.2   Derivation of  Unit Costs  to  Estimate Nationwide Costs of
         Control  Options
      The estimation of nationwide costs of the  control options  makes use of
 a TSDF Industry  Profile data base (assembled to aid  in this effort and
 described in  Appendix  D)  and the  emission control  costs for individual
 source category/emission  control  combinations whose  development is dis-
 cussed in Appendix H.   The Industry  Profile gives  the waste throughput data
 used to assign throughputs to each TSDF waste management  unit in  each
 facility in the  Nation.   To facilitate the use of  these two information
 sources,  the  total  capital  investment and annual operating  cost for  each of
 the model  unit cost estimates were divided by the  throughput of the  model
 waste management  unit  (emission source)  to obtain  a  cost  (both  total
 capital  investment  and  annual  operating cost) per  unit of waste throughput.
 The following paragraphs  discuss  the  development of  the unit cost factors.
      7.1.2.1  Costs  as  a  Function of  Throughput (Unit Cost  Factors).  As
 part  of the effort  to characterize the variety of  TSDF operating  practices,
 model  TSDF waste  management  units were defined.  The main purposes of the
 model  units are to  evaluate  uncontrolled  emissions from waste management
 processes, assess the reduction in air emissions when emission  controls are
 applied,  and estimate the costs of applying  controls.  Model units were
 defined  for TSDF  storage,  transfer and  handling, treatment, and disposal
 operations.  The model units  cover a  range of waste management  unit  sizes
 (e.g.,  throughput,  surface area, and  tank  volumes) and other characteris-
tics  that may impact air  emissions.   The  entire set of model units is
presented in Appendix C of this document.  The approach to  developing con-
trol  costs discussed in Section 7.1.1 was  applied to each of the model
units  listed in Appendix  C for each of the individual unit  emission con-
trols.
                                    7-4

-------
     The next step toward generating the control  costs on a nationwide
basis was to convert the costs of controls for the model  units to a cost
per unit of waste throughput;  i.e.,  the costs of controlling emissions from
each model unit were divided by the annual waste throughput of the model
waste management unit to which the control was applied.  These factors
(referred to as unit cost factors),  when multiplied by the waste throughput
for a particular waste management unit, yield an estimate of the cost of
air emission controls for that unit.
     7.1.2.2  Development of Weighted Cost Factors.  Data contained in the
TSDF Industry Profile (described in Appendix D) are used to estimate annual
waste throughput for each type of waste management unit at each TSDF.  The
Industry  Profile, however, does not yield the exact size of each management
unit, e.g., 758 m3 of tank storage could be ten 75.8-m3 tanks in one case,
or one 758-m3 tank in another case.  Because there are economies of scale
associated with emission control costs, the total control costs might be
substantially different for these cases.  To compensate for the lack of
facility-specific unit size information, weighted unit cost factors were
developed that account for the national size distribution of  TSDF waste
management units.  Statistics on the national distribution of waste
management unit sizes were used to weight the emission control costs for
each model unit size defined  in Appendix  C  (see Appendix H).  This approach
yields  an approximation of the effects  of economies of scale  for the
nationwide cost estimates.
     Table 7-1  lists the  unit cost  factors  used to estimate nationwide
total capital  investment  and  annual operating costs for  each  of the emis-
sion controls  specified  in the control  options.
7.2  SUMMARY OF  NATIONWIDE CONTROL  COSTS  FOR CONTROL  OPTIONS
     This section  presents tabular  summaries of the estimated nationwide
total capital  investment  and  total  annual costs  (annualized capital cost
plus annual  operating costs)  for the five control  options  described  in
Chapter 5.0.   Separate  cost estimates  are given for each TSDF source
category.
     The nationwide cost  estimates  were obtained  by multiplying  the  quan-
tity of wastes managed  in each  TSDF waste management  unit  (obtained  from
                                     7-5

-------
   TABLE 7-1.   ESTIMATED TOTAL CAPITAL INVESTMENT  AND  TOTAL  ANNUAL COST  PER
                UNIT OF WASTE THROUGHPUT BY  SOURCE CATEGORY  FOR
                             FIVE CONTROL OPTIONS9
        Source category
       Total
capital investment,
 $/Mg throughput
      Total
  annual  cost,
$/Mg throughput13
 Drum storage0
 Dumpster storage
 Storage  tanks
 Quiescent surface  impoundments
 Quiescent treatment tanks
 Aerated/agitated tanks and
 impoundments
 Wastepilesc
 Landfills0
 Waste fixation process units
 Incineration0
 Land treatment0
 Spills0
 Loading
 Equipment leaks0
      6.3-26
      9.7-28
      1.9-2.6
     0.22-1.2

     0.41-2.9
       12.3
     2.1-9.9
    4.9-15.0
    0.87-4.8
    0.14-0.58

    0.26-1.7
       5.1
     0.49-0.94
    0.09-0.18
aTotal capital investment includes all costs to purchase equipment, direct
 installation charges, and indirect installation charges.  Total annual cost
 is the sum of the annual operating cost and the annual ized capital costs.
 All costs are in January 1986 dollars.
     unit costs were obtained from information presented in Appendix H.
 Where a cost range is given, the range represents cost variations due to
 differences in waste composition.  Model waste compositions for which costs-
 were derived are presented in Appendix C.
°These sources are not being controlled by the control options presented in
 this chapter.  For further information, see Chapter 5.0.
                                     7-6

-------
the TSDF Industry Profile) by the unit cost factors listed in Table 7-1.
The estimated costs for each TSDF were summed to produce national totals.
Table 7-2 lists the estimated nationwide total capital investment and the
estimated nationwide total annual cost, respectively, for each of the
control options.
     The estimated total capital investment for control options 1 through 5
ranges from a low value of $520 million for option 5 to a high value of
$2.1 billion for option 1.  The estimated total annual costs (i.e.,
annualized costs) for control options 1 through 5 range from a low value of
$210 million for option 5 to a high value of $930 million for option 1.
     The nationwide cost information presented in this chapter provides two
means of comparing control options:  capital and annual costs.  Other means
of comparing options are discussed in Chapter 5.0.  Section 5.5 describes a
methodology for ranking control options according to the relative health
and environmental benefits achieved by the options.
7.3  COST EFFECTIVENESS OF CONTROL OPTIONS
     Table 7-3 shows the cost effectiveness of the five control options.
The cost effectiveness of a control option is defined  as the total annual
cost of applying controls to all emission sources covered by the option
divided by the total emission reduction that would be  achieved.  Total
annual cost is the annual operating cost plus the annual cost of capital
required to purchase and  install the controls.  As shown, the cost effec-
tiveness of options 1 through 5  varies from $130/Mg  to $540/Mg of,  organic
emission reduction.
     Only a single aggregate cost effectiveness is presented for each  TSDF
control option.  The cost effectiveness of controlling specific  emission
source categories covered by an  option  (e.g., the cost effectiveness of
controlling storage tanks)  is not presented.  This is  because emissions
from TSDF sources are  interrelated  in many strategies  and,  consequently,  it
is  potentially misleading to estimate  the cost effectiveness on  an emission
source category  basis.
      For example, covering  only  the first of  several  TSDF waste  management
units  (emission  sources)  in  series will reduce organic emissions from  the
unit  that is  covered but  may increase  the emissions  from  the uncovered
                                     7-7

-------




•V



IH

D_
O

—1
§
f"»

O

tu
^>
M
U-

g
u.

^™
c/?
8

^



g!
h-
O
|
j_

UJ
^t

w
M

5l
S
0-
5
g
Jr
P
r*
Ul

HH
g
C3
M
£

ESTIMATED
CJ
rl
UJ
H






to
cS
«H
n


49
tf!
O
U

II
3
C
C
"
—•
a
49
0
t-







O
c
c

4:
o
o

o
L.
49
C
 C9 «9
CO CO rH rH • CO CO
CM CO CO CM OJ







O O O c9 CO CO O
tO CO • • rH CO CM
rH CM UJ OJ UJ


s s OJ *• i- CM <9
CO 19 rH rH OJ OJ
rH ^- CO

O O CO OJ OJ CS) CS)
CM CO rH CM CM B> CO
rH rH CO OJ



§S CO OJ OJ S (9
T rH CM M S O
CM co eo r—
^


CS> CSt OJ CM Q CS> CSt
CM UJ rH CO CO rH (9
tO CO CO rH
CM"












n
49
4? 4? 0
c n c E
0 49 0 -0
E c e c IA
49 0 4> n 3 49
a £ a .* o —
0 -o 0 c a. c
t C t • E 3
W 49 3 4> 49 —
-* O c
C t- 0. t- 49 49 O
• 0 E 0 C C
49 — 0 0 -O 49
0 0 0 o n m —
49 CD 49 OJ (0 (A L. X a
cm cm 0 0 0.-4>
C L. 01..-.- C 0
O 0 01.
o L. — a
49 a
o— 0 e)
0 a - > c
U 49 (A — O

T> a. a 49
cm 0 49 a.
— 0 — 00
0
TJ-o 49 --
c a c <•- o
a N o 0 u
•— E 1. 49

CA a •— -o o
03 3 CO
OJ c cr a
t- c 0 0
a a m-c
s: -o — (-
00 c o
j: « u
C 49 49 •
O •» C >*-x
— 1» IA O E
49 C — 00.
a a — a.
— 49 'a. o (9 ci
a IA 
3 O IO L.
IT 0 '- 0 - 0
0 .C 49 .C rH 49
49 a 49 IA
0 t- n a
IA<<- 0 C E
a o c o •» 3
.C — Tj
O E O >. •-
1-3 C • — E .
30) •— C9 49 O. 0
a. • c a. a>
0 -to a a
o.c n c C9 t.
49 49 — U — S 0
— 0 E UJ 49
(A (A — 49 O IA
4>— «t- Q. -0 ||
« TJ a 0 E
O 49 C -C t. CO 3
on ao Q. t.
o • — -o -o
— o w c -o c
— t. >— 0 a «
a— a n M 0
e— 0-o a CM -o
(A 3— — 0 .O 3
0 C 0 — 49 •- —
•n c -o o. w « « o
3 a 0— i. o c
— co 49 — a — —
O— CO IA C '
•— 49 rH * C O) L.
O O -C t. • O
49 t- as O)'- O) o S O)
C 1- C 49 3 '0
0 a •- a o E to 49
£ • 3 TJ o t- a. a
49IAC3 ^CLUO
IA 0 a — 9s 49 0
0 OJ-J 0 J« ^S 49^ •
c a c — -o n a t.
— JC— 0 IA .C 3
O — C rH U O
— 0 (A — O ^-^ IA
• C Z C 0 •- C
49 o a o i- 49 IA — «
— — t. 49 O.— 0)
O.49 (A 3 C O OTJ L.
» O 49 O O CO0
O— IA IA O — 49 JJ c
— o o c— —
— ao t-ojt.oi. a
349 0C49UO49
49 IA — JZ— C IA C
OC— 490 O«t-0 O
1- — < o^ oo-o u
a ja o -o
7-8

-------
  TABLE 7-3.  NATIONWIDE TSDF COST EFFECTIVENESS OF FIVE CONTROL OPTIONS
     Control option13
  Cost effectiveness,
$/Mg emission reduction
           1

           2

           3

           4

           5
          540

          420

          220

          170

          130
aThis table presents total annual costs of control divided by organic
 emission reductions, i.e., cost effectiveness.

^Control options 1 through 5 are based predominantly on the use of add-on
 emission controls.  The control options are described in Chapter 5.0.
                                    7-9

-------
              units  downstream,  resulting  in  no change in  total  facility  emissions.   The

              cost effectiveness of  controlling the  first  unit may  look  attractive  in

              isolation,  but,  as a practical  concern,  reduction  in  total  facility emis-

              sions  would not  be achieved  unless units downstream were controlled as
              well.

              7.4  REFERENCES
              1.




              2.


              3.


              4.


              5.


              6.


              7.


             8.
U.S. Environmental Protection Agency.   EAB  Control Cost Manual  (Third
Edition), Section 2:  Manual Estimating Methodology.   Publication No.
EPA-450/5-87-001A.  Office of Air Quality Planning and Standards,
Economic Analysis Branch.  February  1987.

Vatavuk, W. M., and R. B. Neveril.   Chemical  Engineering.   165-168.
October 6, 1980.
Vatavuk, W. M., and R. B. Neveril
November 3, 1980.

Vatavuk, W. M., and R. B. Neveril
December 29, 1980.

Vatavuk, W. M., and R. B. Neveril,
May 18, 1981.

Vatavuk, W. M., and R. B. Neveril,
January 24, 1983.

Vatavuk, W. M., and R. B. Neveril,
April 2, 1984.
Chemical Engineering.  157-162.


Chemical Engineering.  71-73.


Chemical Engineering.  171-177.


Chemical Engineering.  131-132.


Chemical Engineering.  97-99.
Mahoney, W. D. (ed.).  Means Construction Cost Data.  Kingston, MA,
R. S. Means Co., Inc.  1986.
_
                                                 7-10

-------
                            8.0  ECONOMIC IMPACTS

     Chapter 5.0 describes five control options for organic air emissions
from treatment, storage, and disposal facilities (TSDF).  This chapter
estimates the economic impacts of control options 1 through 5.  For
analytical purposes, it is useful to divide the affected facilities into
those that only have hazardous waste storage facilities and those that also
perform treatment or disposal services.
     All control options examined are projected to have small impacts—less
than 1 percent—on the unit cost of hazardous waste management services at
facilities that treat and dispose of these wastes.  These unit-cost
increases will slightly raise the costs and prices of goods and services
produced by the generating sectors.  This will encourage a small amount of
waste minimization.  The capital costs will vary between $500 million and
$2 billion for these facilities; annual compliance costs will vary between
$200 million and $900 million.  Small decreases are projected in the number
of jobs at TSDF, so small that employment dislocations will probably be few
if any.  Similarly, while the projected reductions in waste generation
could, in the aggregate, imply facility closures, it appears much more
likely that the reductions will be distributed across all facilities and
that the number of closures, if any, will be nominal.
     The unit-cost increases for storage-only facilities are substantial
for several sectors and options when viewed as a share of hazardous waste
management costs.  These cost increases translate into compliance costs of
between $4 million and $31 million.  However, storage facility closures
again appear unlikely, even though there may be some economic pressures in
that direction, because closing a permitted facility requires the firm to
undertake a time-consuming and expensive process.  This process is designed
to ensure that  liability rules are met and that the environment is pro-
tected from hazardous wastes.
                                     8-1

-------
8.1   INDUSTRY PROFILE
      Before beginning the economic analysis, it is necessary to define the
affected industry.  The following sections discuss the activities of haz-
ardous waste managers and describe the markets where they are active.  The
demanders and suppliers of these services are described, along with the
factors underlying their production and consumption decisions.  The size of
firms operating the hazardous waste management facilities, along with other
characteristics relevant to the economic analysis model, are also pre-
sented.
     The demand for hazardous waste management services is a function of
the production process.  In the course of producing final goods or ser-
vices, firms often produce hazardous waste.  Because these production
outputs are technically interdependent, they are referred to as "joint
products."
     The firms that produce hazardous wastes as joint products with their
product or service represent more than 100 different Standard Industry
Classification (SIC) codes.  The hazardous wastes they produce represent
more than 400 Resource Conservation and Recovery Act (RCRA) waste codes.
Hazardous wastes include characteristic wastes, wastes from both specific
and nonspecific sources, chemical products and intermediates, and discarded
chemical products and residues.
     Because these wastes are classified as hazardous under RCRA, they must
be treated,  stored, or disposed by a permitted TSDF.  A generator can
treat, store,  or dispose, hazardous wastes on site if it has a permit, or
hire a commercial TSDF to manage its hazardous wastes.  To reduce the
demand for hazardous waste management services, generators may reduce the
level of waste generated.  Generators may reduce output levels of the
primary product or substitute other inputs in the' production process to
reduce waste and, hence, the need for waste management services.
     The following industries generate wastes in their production processes
and, therefore,  produce not only their marketable commodity but also haz-
ardous wastes:
     •    Mining
     •    Milling
                                     8-2

-------
     •     Manufacturing  of  chemicals  and  Pharmaceuticals
     •     Manufacturing  of  primary  and  fabricated  metals
     •     Manufacturing  of  cement
     •     Manufacturing  of  electrical  and nonelectrical machinery
     •     Manufacturing  of  transportation equipment and instruments
     •     Electric and gas  utilities
     •     Wholesale and  retail  sales
     •     Research labs, hospitals, university research centers
     •     Remainder of the  economy, including government  facilities.
     On the supply side of  the market for hazardous waste management
services are many of the same firms that generate the hazardous waste and,
therefore, appear on the demand side of the market.  These firms provide
"captive" onsite hazardous  waste management services.  In addition to these
captive firms, a group of commercial  firms specializes in managing hazard-
ous materials.  Section 8.1.1 describes the suppliers of  hazardous waste
management services in more detail.
8.1.1  The Supply Side
     Hazardous waste management processes fall into three major categories:
(1) treatment, (2) storage, and (3) disposal.  Within each of these cate-
gories are further subcategories totaling 12 waste management processes.
TSDF can be classified  into four broad categories:   (1)  captive storage-
only facilities;  (2) commercial storage-only facilities;  (3) captive TSDF;
and  (4) commercial TSDF.  Storage-only facilities  (captive or commercial)
store the wastes  using  containers  and/or tanks prior to treatment and
disposal; TSDF (captive or commercial) include all facilities other than
storage-only  facilities (captive and commercial).
     8.1.1.1  Hazardous Waste Management Processes.  Hazardous Waste
management services include storage, treatment, and  disposal of wastes
described in  Table 3-1  and Table 3-2,  Chapter 3.0.   Twelve processes are
identified.
     The  key  storage  processes  include containers, tanks, wastepiles, and
surface  impoundments.   The key  treatment processes include tank treatment,
                                      8-3

-------
 surface impoundment treatment,  incineration,  and other treatment.   The key
 disposal  processes include injection wells,  landfills,  land  application,
 and surface impoundments.
      8.1.1.2  Costs of Hazardous Waste Management Processes.   The  costs of
 a hazardous waste management process include  all annual  costs  (e.g.,  raw
 materials,  utilities,  labor, maintenance,  and overhead)  required to operate
 a plant.   Typical  plant sizes and typical  operating practices  were identi-
 fied for  each  of the 12 management processes  to develop  generalized cost
 equations.   The annualized average costs  of hazardous  waste management
 processes ($/Mg of waste managed)  were estimated for each  of the 12 waste
 management  processes.
      The  operating costs of waste management  processes were obtained  from
 several sources,  including studies by Booz-Allen and Hamilton; Research
 Triangle  Institute;  Industrial  Economics,  Inc.;  Temple,  Barker, and Sloane;
 and  the National  Council of the Paper Industry on Air  and  Stream Improve-
 ment.  As with  some of  the other data,  process costs reflect recent but not
 necessarily current values.   For each of the  12  processes, model costs were
 developed for different plant sizes  using  available information on  model
 and  actual  process expenditures.   In  this  manner,  cost estimates were
 determined  for  the different waste management  processes.
     The  per-metric  ton processing costs for  the 12 different waste
 management  processes were  compared with values found in  other sources  to
 verify their reasonableness.  The  results  of  this  comparison are presented
 in Table  8-1.   As  can be seen from the blank  entries in  the table,  not
 every source gives  costs estimates for each process  technology.  It is also
 evident from the tables that, in most cases, the RTI cost estimates are
 comparable  to those of  the other sources.
     Finally, the  cost  functions were developed  using unit costs developed
 for the 12  different waste management processes  and  several plant sizes.
The estimated parameters of  the cost  functions are  summarized in Table 8-2.
These cost  functions were used to  compute  costs  for waste management opera-
tions in TSDF from which price adjustments resulting from the control
options were estimated.
     8.1.1.3  Identifying Directly Affected Facilities.  From the Industry
Profile discussed  in Appendix D, 2,336 facilities were identified that
                                     8-4

-------












2*
o
r—
M
P"
En
3t
ffi
Q.

r-
O
U
TH

^
ii
O
z

1
i
j^



!

CO
tu
m


















M /-^
ceC*
U. Hi CO
O '-'CO
£ C


0
C « 0
a 
— a TH
Q. O>^
0 (O



— - '
•- o vt
L. — •
4> E O •»
IA o c m
3 C M O>
•DO TH
CO •^
M 111




_ ^^

a 0
3 > TH
t. CO
< 3 OJ
rH (/> rH
Q- ^




C
0 C x^
— O «»
— TJ -P
< C — CM
i a ••• co
N E 0>
o a TH
o x ^
m





£
O
1 «
Waste
management pri
base 1 i n<
_O
O) O> CO CO
•*• •» eo to
0> O> CM TH
1 1 1 I
CO CO 0> 0>
• TH CO
SO TH

M CO
• CM CM ^
O) O> O> •
r*. r*. t*. fH -

1 1 I 1
•of CO Q CO
CO • i-*
CM M  &
CO  19
00 IS
rH fH


CO

tH CO rH

* t 1 1
CO U> CO
^ *f »H
* tH •
CM 0


CM B&

O O> Q
h. CM h»
III*
r * u
CO O TH
CM CO




CM CM
* 1 1 *
Q co
8 s



49
c

M TJ
c c
o -P 3  C 0 Q. O
^ £ -5 ^ t»3
•P a o ' Q
43 a 0 -P 4» O
c 0 t. a c
JU -P 1- 0 0
•p 0 E a
i. c -P a
a .x 0 •— a t-
0 C -C O 0 O
t. a -P c t. -P
1- H O M 1- W
O CO S
CO CO
i~. r-- •>!• s
ID IO f-- O)
1 1 1 1
^ Q) IO tO
co en TH •
CM CM -CO
CO TH

&
§ CO TH
TH CO -
eo TH
S 1 1
fH 1
co eo
CM fH CO
• to co
to


* * * *






CO O
CM TH
r*» •»
eo eo TH
5> ia i
TH TH 1
CM
• co
IO TH


to
§ ^
CO CO
CO
* CM 1 1
IO CO CO
to co
TH






* » » *







* * * *






4)
0 £
CD EM
a -o c
L. CO
O 3 —
4> 0 O -P
no Q. a
• WE O
« k • ~
c $ ~ 0 a
— at Q. u>  j: -P u a
c c « o n
o a a -P
o I- * OT a
^
co to
00 f*** O
CM LO O)
00
1 1 O f
(O CO CO U3
r^ co co
to to TH


*• h- to to
V TH CO »H
i-i ID r~ co

i i t i
IO TH rH CO
CM •» fH tO
ID ID ID T
^
TH
1 » * *
f-J
CO
TH




C- to
•H CO
to r«-
* t i *
s to
to


CM
• s* o to
Q tO U) fH
CO fH TH CO

1 1 1 1
CO CO TH CO
CM O tH CO
TH IO
CO



CO
co
TH
CM CO
• 1 * tO
O9
to



00 6}
co to co
CM t«- CM
III*
IO 5> CM
CM • •
• • co co
IO CO rH




43
C
1
C
•P — 3
C < — 0
0 ce 0 a.
1 - i I
i_ — .— a
43 ._ 4) g)
 n
a a c —
_J _1 IH Q


a
0)
o
a.
(A
-tj
•D
C
a

0
en
a
|
c
|
0
<_
0
(A
0
X
01
•3
o
"O
a
N
a
.c
i_
o
(A
0
U
L.
3
O
CA
(A
3
O
U
a


g

i_

VI
-p
(A
O
O
0 -p
0 —
1. C
3 3
O
0) TJ
0
at -P
il
ll
«T- 0

0 -p

^> m
a -P
^ c
a 
(A
•P O
c u
co -P en
i a a
TH C I.
• t- O
fA 4» -P
c «
o <-
— 0 Jf
4» ^ C
o. -P a
0 0 r-
ja o
8-5

-------
            TABLE 8-2.  PARAMETERS OF THE UNIT COST FUNCTION3
       Waste
management practice
     baseline
Intercept
Slope
Treatment options

Tank treatment
Other treatment
Incinerator-
Treatment impoundment

Storage options

Container storage
Tank storage
Wastepiles
Storage impoundment

Disposal options

Land treatment
Landfill RCRA
Injection well
Disposal impoundment
  8.60
  8.60
  8.78
  8.70
  7.09
  8.70
  7.58
  7.09
    0
  9.43
  10.4
  8.70
0.60
0.60
0.65
0.56
0.44
0.56
0.26
0.44
6.98
0.50
0.66
0.56
aThe unit cost function depends on the amount of waste processed and
 the type of waste management processes used.  The function was esti-
 mated using the available data described in Table 8-1.  The function •
 was assumed a log-linear function,  defined by: C(Q) = a - b ln(Q),
 where a and b are the estimated intercept and slope values, Q is the
 amount of waste processed,  and 'In'  represents natural logarithm.  The
 unit costs are truncated by the upper and lower bounds represented  in
 the last column of Table 8-1.   The  estimation of the parameters of  the
 cost functions are described in Reference 7.
                                   8-6

-------
performed some form of hazardous management service in 1985.  Out of 2,336
facilities, 2,002 are estimated to produce organic emissions.  Of these
facilities, 1,098 facilities were storage-only facilities; the remaining
904 facilities provided all forms of hazardous waste management services.
Nearly 70 of the 904 facilities were either government facilities or
facilities listed under service industries.  The economic analysis includes
only the remaining 834 directly affected facilities.  The excluded storage-
only facilities (1,098) and government facilities (70) represented less
than 5 percent of the total waste volume serviced by all the 2,002
facilities.  In addition, the compliance costs of the excluded facilities
comprised less than 1 percent of the total compliance costs in all options.
The summary statistics by directly affected facilities, storage-only
facilities, and government facilities are presented in Appendix I.
     These directly affected facilities (834) were found in more than 100
different industries, as described by their 4-digit SIC code.  To facili-
tate the economic analysis, the TSDF were grouped into 20 generating sec-
tors and 1 commercial treatment sector.  The 834 facilities were assigned
to one of the 21 market sectors, based on their primary product or service
as indicated by their SIC codes.  In 20 of the 21 sectors, firms generated
as well as treated, stored, or disposed of hazardous wastes.   In the 21st
sector, the commercial sector, facilities only supplied hazardous waste
management services to firms in the other sectors.  Table 8-3  lists the  20
generating sectors and the 1 commercial sector, along with the number of
facilities in each sector and the volume managed by each sector.
     The supply elasticities of hazardous waste management services, which
measure the responsiveness of-an industry's quantity supplied  of hazardous
waste management services to changes in the price of these services, are
shown in Table 8-4.  To compute these elasticities, unit cost  estimates
were first developed for each of the 12 processes using engineering rela-
tionships and costs.  These cost functions are only valid for  the range  of
output for which data are available; at very  low outputs and very high
outputs they give unreliable results.  Therefore, the cost function was
truncated using judgment and information about the costs of  actual hazard-
ous waste management firms.  The cost curve is shaped  like a backward  L.
                                     8-7

-------
            TABLE 8-3.  VOLUME OF WASTE MANAGED BY SECTOR, 1986a
     Sector
Number of
facilities
Volume managed,
   103 Mg/yr
Mining                                               12
Grain and textile mill products                       4
Furniture, paper products, printing                  35
Industrial chemicals, inorganic and organic         139
Plastics, fibers                                     39
Biological, pharmaceutical, medical chemicals        20
Assorted chemical products                           54
Paint and allied products, petroleum and coal        99
Rubber, plastics                                      7
Cement companies                                     11
Primary metals                                       70
Metal fabrication                                    67
Nonelectrical machinery                              15
Electrical machinery and supplies                    45
Transportation equipment                             29
Instruments                                           8
Miscellaneous manufacturing                           5
Electric and gas utilities                           24
Nondurable goods:  wholesale sales                    4
Research labs, hospitals, universities               11
Commercial hazardous waste handlers                 136

     Totals                                         834
                    92.8
                   130.0
                    38.3
                99,600.0
                53,900.0
                 2,820.0
                20,800.0
                 6,740.0
                     5.4
                    36.0
                 1,960.0
                 1,070.0
                    42.3
                   514.0
                   764.0
                    29.8
                   260.0
                   340.0
                    60.6
                     0.2
                 5,720.0

               195,000.0
aThis table groups each of the 834 facilities included for the economic
 analysis into one of the 21 market sectors (20 generating sectors and 1
 commercial sector).  Facilities included in the generating sectors gen-
 erate and manage (treat and/or store and/or dispose) hazardous wastes.
 Facilities included in the commercial sector only supply hazardous waste
 management services to the generating facilities.  Data are taken from
 the Source Assessment Model (SAM) Industry Profile data base, Appendix D,
 Section D.2.1.
                                     8-8

-------
       TABLE 8-4.  SUPPLY ELASTICITIES FOR HAZARDOUS WASTE MANAGEMENT
                             SERVICES BY SECTOR3
     Sector
Supply elasticity
Mining
Grain and textile mill products
Furniture, paper products, printing
Industrial chemicals, inorganic and organic
Plastics, fibers
Biological, pharmaceutical, medical chemicals
Assorted chemical products
Paint and allied products, petroleum and coal
Rubber, plastics
Cement companies
Primary metals
Metal fabrication
Nonelectrical machinery
Electrical machinery and supplies
Transportation equipment
Instruments
Miscellaneous manufacturing
Electric and gas utilities
Nondurable goods:  wholesale sales
Research labs, hospitals, universities
Commercial hazardous waste handlers
      0.55
      1.82
      0.47
      0.10
      0.03
      0.03
      0.38
      0.16
      0.05
      0.46
      0.13
      0.08
      0.15
      0.54
      0.07
      1.26
      0.00
      0.17
      0.01
      0.66
      .0.29
aThe supply elasticities of hazardous waste management services in this
 table measure the responsiveness of a sector's quantity of hazardous waste
 management services to changes  in the price of these services.  Step
 supply functions for each of the 21 sectors reported in the table were
 constructed using the waste management cost functions reported in
 A Profile of the Market for Hazardous Haste Management Services, a
 1986 draft report prepared by Research Triangle  Institute for the
 U.S. Environmental Protection Agency, Office of  Air Quality Planning
 and Standards, Research Triangle Park, NC.  A log-linear regression was
 performed to estimate the elasticities.  Data are taken from the Source
 Assessment Model  (SAM) Industry Profile data base, Appendix D,
 Section D.2.1.
                                      8-9

-------
Up to the capacity volume of throughput, the marginal cost curve is hori-
zontal  (perfectly elastic); beyond that volume, vertical  (perfectly
inelastic).
     Each facility's marginal cost (= average cost) of hazardous waste
management service was calculated based on the volume of  hazardous waste
management service.  Then, ranking facilities from the lowest unit cost to
highest, the volumes of hazardous waste management services were accumu-
lated across all the firms in the sector.  This process results in a
"stepped" supply function for each industry sector.  After constructing
these stepped supply functions for each sector, a log-linear regression was
performed to find a constant elasticity of supply for each industry as
reported in Table 8-4.
8.1.2  The Demand Side
     As mentioned earlier, the demand for hazardous waste management
services arises because, in the course of producing their final goods or
services, firms may also generate hazardous wastes.  The majority of the
facilities generating hazardous wastes as a result of their production
                                                                           ;
process are chemical manufacturers.  In all, however, firms in more than
100 4-digit SIC codes demand hazardous waste management services.
     Many facilities choose to recycle or incinerate their own hazardous
waste on site, for a variety of reasons.  Not all of these reasons are
directly related to management costs.  Under RCRA, generators retain some
liability for the waste they generate after it leaves their facility.
This undoubtedly induces some firms to reduce their risk by keeping the
hazardous waste on site.
     However, not all of the facilities generating hazardous wastes choose
to manage them entirely on site.  Rather, some use the services of commer-
cial waste management firms.  It is assumed in this analysis that all the
demand for hazardous waste management services originates in the first 20
generating sectors listed in Table 8-3.  Some of the demand is met by the
generators themselves, while other firms in these same generating sectors
use the services of commercial waste management facilities.  The firms in
the generating sectors that have RCRA permits are assumed here to manage
all their own hazardous wastes on site.  All other firms within these
                                    8-10

-------
sectors are assumed to ship hazardous wastes off site to commercial  waste
management facilities.
     To estimate total consumption of hazardous waste management services
in each generating sector, it is necessary to sum the consumption that is
met by onsite management with the sector's estimated share of commercially
supplied management services.  No information is available about commercial
consumption arising in each of the generating sectors.  It is assumed that
all the demand for these services arises from the same 20 sectors that
perform onsite captive management.  The total commercially supplied hazard-
ous waste management services are allocated across the 20 sectors based on
the ratio of each sector's transported waste quantities to the total quan-
tity transported by the 20 sectors.  Table 8-5 shows the 20 demanding
sectors, along with the total volume that each sector services commercially
or on site, and the grand total of hazardous waste management demand origi-
nating in each generating sector.
     To simplify the economic analysis, it is assumed that each firm uses
only two inputs to produce its output: hazardous waste management services
and one other composite input.  Table 8-6 shows the estimated share of each
industry's total production cost attributable to hazardous waste management
services.
     A measure of the price elasticity of demand for the products of each
generating sector is needed for the economic analysis.  Price elasticity of
demand measures the percentage change in quantity demanded in response to  a
percentage change in product price.  The elasticity of demand for interme-
diate products such as those produced by all the firms in the data  base
depends on several factors related to the final product.  First, because an
intermediate product  is used to produce a final product, the demand for the
intermediate product depends on the demand for the final product in which
it  is used.  Thus, the demand for a chemical depends on the demand, for
example, for the paint, pharmaceutical product, or plastic product  it  is
used to produce.  The degree of variation in quantity demanded  of the
intermediate product  in response to a change in its price thus  depends,  in
part, on the responsiveness  of the final product's quantity demanded  to
changes in  its price.   It also depends on the  cost share of the final
                                     8-11

-------
 O
 a.

 35
UJ

£





I

%
 I
CO
     CD

     u

     >


     i


    I
     u
     0
     ID

    JC
     o
     a
     0
JC   -O    O>
 O   0  X C
 a   43  i	
 0   i.  a 43
     o  ID a
 C X DL CO t.
— Jj o>  0 0
     cue
 C9T) a  0 0
 c 0 t.  c o>

43 3    MS
 a o. ID  a CM

 =Jl*.
 O)   O  C J=

'«- a o —
 O * ffl 43 <*-
     «  a o
   w   43
                                                                                              c u .
   p u  a. o
     S.S 2
                                                                                                            o

                                                                                                             X
                                                                                                             c
                                                                                                             0
                                                                                                             a.
                                                                                                             Q.
 0
 ID
 a
 J3


 a
 43
                                                                                                             O
                                                                                                             L.
                                                                                                            o.


                                                                                                            ^

                                                                                                             CO
                                                                                                             3
                                                                                                                  !
                                                                                                                   Q.

                                                                                                                   0
                                                                                                                  Q
                                                                                                                  U


                                                                                                                  O
                                                                                                                  JC
                                                                                                                   w
     i  o CD a o
           3 Q.
     i	tr w
       a a   c
     .43 •- TJ a
    5-0 fa'
      43 n a   —
         E •	a
      -o 3 o a  >
      c — t- 43  a
      a o 0 o
         > E 43  ID
                                                                                           0

                                                                                       0  5
                                                                                             < 0 0
                                                                                             43JCU
                                                                                             — |-
             0
             JCC
             43  O
                                                                                       JJ
                                                                                       a
                                                                                       u
 Q.
 &  -5
43  -S



!i
Z  a
     a o 43
 C • 43 43 a
 o t- o   E
   o 43 CD u
 t. 43   0O
 O O 0 — «l-
   0 J= 4> C
 X CD 43 — —
—     4>
— O) O) C O
 a c c a c

'o 43 43 CT 0 0)
 L. a a   wi.
 O L. U 0 3 O
 i 0 o 43 a 43
 E c — « o o
 o 0 — a 0 0
 u co a £ -a ID
                                                                                                             0
                                                                                                            -o
                CD



                0
                O
                L.

                3
                O
               W
 0 i-J


 IH

 0 °
 L. C
 a o

 a 43
 43 O
 a «
j>co
             o
             o

             O)
       ID     C

       CD     0)
       C     3

         eg  «>
         CO  0
       0 o>  —
       J= 1-1  43
       43     —

       g M  *v

       O 3  O
       US)  9

       -g  *•



       10  .?
       a jz  43
       43 43  a

       0 «H  O
       I- O

         3  -O

       23  c
       at.  o
       Q 3  —
         CO  43
                                                                                                                     .  t
                                                                                                                  0  U
                                                                                                                  3  L.
       c
       o

 > i
   o  —
CM u   a
CO    43
O) «*•   O
rH O  t-
O    TJ
                                                      8-12

-------
         TABLE  8-6.   COST  SHARES  AND  DEMAND  ELASTICITIES  BY  SECTOR9
Sector
Mining
Grain and textile mill products
Furniture, paper products, printing
Industrial chemicals, inorganic and organic
Plastics, fibers -
Biological, pharmaceutical, medical chemicals
Assorted chemical products
Paint and allied products, petroleum and coal
Rubber, plastics
Cement companies
Primary metals
Metal fabrication
Nonelectrical machinery
Electrical machinery and supplies
Transportation equipment
Instruments
Miscellaneous manufacturing
Electric and gas utilities
Nondurable goods: wholesale sales
Research labs, hospitals, universities
Commercial hazardous waste handlers
Cost share of
HWM services,
x 10-3
0.5
1.4
0.4
84.6
180.0
14.1
43.1
1.6
*
1.5
1.9
1.8
0.1
1.1
1.1
0.2
2.6
0.1
0.4
*
NA
Demand
elasticity
-0.70
-0.70
-0.70
-0.67
-0.16
-0.89
-0.87
-0.23
-0.13
-0.70
-0.70
-0.70
-0.19
-1.05
-0.83
-0.70
-0.96
-1.90
-0.70
-2.92
-2.41
* = Less than 0.05.
HWM = Hazardous waste management.
NA = Not applicable.

aThe cost-shares and price elasticities reported in this table are the key
 parameters of the analytical model used to estimate the economic impacts
 of the air emission regulations.  The cost-share of the hazardous waste
 management services of each of the generating sectors represents the
 ratio of the costs of hazardous waste management services to the value
 of shipments.  The price elasticities of demand in the table are obtained
 from the Iiterature.8f9  Qata On the value of shipments are taken from
 the Census of Service Industries, Washington, D.C., U.S. Department of
 Commerce, Bureau of the Census, 1982.
                                    8-13

-------
 product this intermediate product represents.  The elasticities  of demand
 used in the model  are found in the literature.10!11  They are less than
 zero because an increase in the price of the commodity results,  other
 things being equal,  in a decrease in the quantity demanded of the  commod-
 ity.  For those sectors whose elasticity of demand is not available in the
 literature,  -0.7 is  assumed.  This figure is consistent with  the range of
 elasticities found in the literature for other sectors.  These price elas-
 ticities of demand for hazardous waste management services are shown in
 Table 8-6.
 8.1.3  Market Outcomes
      The market forces represented above in the supply of and demand for
 hazardous waste management services result in a market solution  for the
 quantity of each type of hazardous waste management service undertaken in
 each sector and the  price of each type of management service.  The baseline
 situation in these markets is the quantities for 1986 as shown in  Table
 8-5.   In a  competitive market,  the market price for hazardous  waste manage-
 ment services would  equal  the marginal  cost of the highest cost  supplier.
 Of course,  most TSDF do not offer the service on the open market.   Only the
 hazardous waste management services performed by the commercial  sector
 actually pass through the market.   The commercial  TSDF were ordered by
 their marginal  cost  and the marginal  cost of the highest-cost  facility was
 selected as  the market price.   The price selected,  $l,280/Mg,  furnishes a
 baseline price against which the compliance costs  of hazardous waste man-
 agement  resulting  from the options may be compared.
 8.2   ANALYTICAL APPROACH
      This study estimates  the economic  impact of regulatory options  on air
 emissions from hazardous waste  TSDF,  with special  attention to the possible
 facility closure effects.   The  primary  emphasis  of the economic  analysis is
 a multimarket partial  equilibrium  model  of the hazardous  waste management
 industry.
      For the  economic  analysis,  the 834  directly affected  facilities in the
 20 generator  sectors  and 1  commercial  hazardous  waste  management sector
were  analyzed.   The  1,098  storage-only  facilities  were excluded  from
 detailed  economic  analysis  because  they  represent  less  than 4  percent of
                                    8-14

-------
the total compliance cost of all TSDF and less than 3 percent of the quan-
tity of hazardous waste managed by all the TSDF.  The costs of compliance
for storage-only facilities are estimated and presented in Appendix I,
Section 1.2.
     For each TSDF in the data base, the costs of implementing the emission
controls were estimated.  These costs are expressed as changes in capital
and operating expenses incurred by the plants as a result of complying with
the control options.  Using this compliance cost information, the economic
effects of the air emissions regulation on TSDF were then projected.  The
following impacts were projected:
     •    Price and quantity changes in affected markets
     •    Annual regulatory costs
     •    Employment effects
     •    Facility closures (if any)
     •    Small business effects.
     The economic theory and operational model underlying this analysis are
discussed in this section.
8.2.1  Model Overview
     To estimate the impacts of the regulatory options, a comparative
statics model, based in traditional microeconomic theory, was used.  The
term "comparative statics" means that a snapshot is presented of all of the
affected markets in their baseline condition.   It is then compared to
another snapshot of the same markets after all of the adjustments have
taken place in response to the controls.  The market for the services of
TSDF was assumed to be competitive.  TSDF were assumed to operate in a
profit-maximizing manner, and to have complete knowledge of all the markets
in which they participated.
     Decisions made by TSDF can be broken down  into two broad categories:
     •    Existing plant and equipment operating decisions, frequently
          referred to as short-run decisions
     •    Investment decisions for new plants and equipment, fre-
          quently referred to as long-run decisions.
                                    8-15

-------
      Short-run  or operating  decisions  concern  the  quantity of a good or
 services  the  firm produces to  achieve  the  greatest  profit, or the smallest
 loss.   In general,  a  firm will  continue  to produce  as  long as the price
 received  for  its  good or services  is sufficient  to  cover the average vari-
 able, or  operating, cost of  producing  it.   As  long  as  price exceeds average
 variable  cost,  the firm is covering the  costs  of all of its variable inputs
 and  some  of its capital costs  as well.
      Long-run or  investment  decisions  require  different reasoning.  Because
 the  investment  in plant or equipment has not been made, that cost too is
 variable.  For  the firm to decide  to invest in a new machine or plant, it
 must expect that  the  price it  will receive for the  goods or services pro-
 duced by  that machine or plant  will be sufficiently high to cover all of
 the  costs  associated  with producing it,  including both the cost of purchas-
 ing  the plant or  equipment and  a normal  rate of  return on the plant or
 equipment.  In  other  words,  the market price of  the good or services must
 at least  equal  the plant's average total cost.   The plant is not yet in
 place, so  all inputs,  and hence the scale  of the plant, are variable.
     At any given time, the  firm's supply  curve  is  its marginal cost curve
 above its  average variable cost curve, and  the market  supply curve is the
 sum  of the existing firms' supply curves (see Figure 8-1).  The willingness
 of different plants—with different average variable costs of production--
 to produce at different market  prices results in the familiar upward slope
 of the market supply  curve.  Firm 1 has the lowest  operating costs, firm 4
 the  highest in  Figure 8-1.   The market price is  determined by the intersec-
 tion of the market demand and market supply curves.  The marginal plant is
 that plant whose  average operating costs just equal market price.  If
market price were  to decrease,  the marginal plant would close.
     A regulation  limiting air  emissions from TSDF  will increase both the
 capital and operating costs  of  these facilities.  It is likely that the
 increase in costs will be greater per unit  produced for existing plants,
which must be retrofitted in order to comply with the regulation, than for
new plants, which can design their equipment to  comply.  In addition, capi-
tal costs may be  higher for  small firms than for larger firms making the
same change in equipment.   This may be true because the interest rate
                                    8-16

-------
Price/Quantity
($)
                                                                                 MC4
                                                                                        AVC4
               Note: In this market, firm 4, whose average operating costs exactly equal market price,
                     is the marginal firm.

                             MC  = Long-run marginal cost curve (for firms 1 through 4)
                             AVC = Average variable cost curve
                             P*   = Market price
                             Q*   = Quantity produced (output) at price P*
                             D   = Market demand curve
                               Figure 8-1. A market supply curve constructed by
                                       summing four firms' supply curves.
                                                  8-17

-------
 charged these smaller companies  is  higher than  that  charged  larger  com-
 panies.  For example,  while larger  companies  may  be  able  to  issue bonds
 (and have higher bond ratings  and,  hence lower  financing  costs than smaller
 companies),  smaller companies-more  frequently must borrow funds  from a
 bank.   In fact,  if their credit  rating  is sufficiently  low,  the  smaller
 company may  not  be able  to  obtain a loan for  pollution  abatement equipment
 at  any  acceptable rate of interest.   Finally, economies of scale in compli-
 ance are usually found,  so  small facilities may have higher  unit compliance
 costs than large facilities.
     The initial  impact  of  the regulation will  be in the  directly affected
 market—the  market for hazardous waste  management services.  The increased
 costs resulting  from complying with  the new air emission  standard will
 cause each firm's  supply curve,  and  therefore the market  supply curve, of
 hazardous waste  management  services  to  shift  upward.  With a smaller
 supply,  a higher market  price  is then required  to justify  producing any
 given level  of output.   The new  equilibrium price will be  higher and the
 new equilibrium  quantity of services produced less than would have  been the
 case in  the  absence  of the  regulation,  all else being equal.  Because the
 cost of onsite hazardous waste management  services is higher than in the
 absence of the regulation,  generators may  reconsider their decision  about
 whether to manage  waste  on  site or off  site.  .If  the cost  of their  onsite
 management increases  sufficiently, offsite hazardous waste management
 services  may become more economical.  They may  also  decide to alter their
 production process to  reduce the quantity  of  hazardous waste management
 services  they require.
     In the market for the  firms' primary  products,   the supply curve will
 also shift upward.  This  is because hazardous waste management is an input
 to their  production process, and its cost  has now risen.   It will now cost
more to produce a  given  output than without the regulation, resulting in
 higher prices and  lower  output rates.   Figure 8-2 shows these changes.
8.2.2  Model  Design
     To assess the impact of the control options,  a model  of 82 simultane-
ous equations, designed to capture the major market  interactions of  firms
in the affected industries identified earlier, was constructed.  This model
                                    8-18

-------
Price/Quantity
($)
                                                       Q2    Q,
                                                     Quantity/Time
                                             •   Preregulation price
                                             •   Postregulation price
                                             •   Preregulation quantity (output)
                                             =   Postregulation quantity (output)
                                             •   Preregulation supply
                                             =   Postregulation supply
                                             »   Market demand
                                             -   Demand elasticity (percent change in demand
                                                quantity for 1 percent change in price)
                                      6      =   Supply elasticity (percent change in supply
                                                quantity for 1 percent change in price)

                 Figure 8-2. Hypothetical price and output adjustments due to a market supply
                                    shift induced by air emission regulations.
U1
Q2
D
1}
                                                      8-19

-------
              is  only for hazardous  waste management facilities  that,  in  addition  to
              providing  storage,  treat or dispose of hazardous wastes.  Storage-only
              facilities are addressed separately in Appendix  I,  Section  1.2,  by simply
              summing compliance  costs.
                   When  such a regulation is  promulgated,  its effects  are felt throughout
              the economy.   The major impact,  however,  will  be felt  in  the active  markets
              of  firms directly affected  by the regulation.  Other markets both upstream
              and downstream from the directly affected markets  will experience smaller
              impacts.  It  is  beyond the  scope of this  analysis  to detail  every activity
              of  every industry in these  markets;  rather,  the most important trends and
              characteristics  of  each directly affected market are incorporated.   The
              model  is based on research  by Muth,12  Miedema,13 and Gardner.14  Specific-
              ally,  it includes equations describing the industries' output markets and
              input  markets  for hazardous waste management services.   Firms in these
              markets  will bear the  major impact of  the regulation.
                  The model of TSDF is a comparative statics model.   It  portrays  the
              impact of  the  control  options on the markets most  directly  affected,
              assuming that  all other conditions in  the markets  remain  unchanged.  For
              example, the prices  of inputs other  than  hazardous waste  management  ser-
              vices  are  assumed constant,  as  is  technology.  The only thing that changes
              initially  is the  cost  of hazardous waste  management services, which
              increases  as a result  of the proposed  regulation.  It  is  assumed that all
              of  the affected markets  simultaneously arrive  at new equilibrium positions.
                  The firms performing hazardous  waste management services find that, as
              a result of the control  options,  their cost  of doing business increases.
              This,  in turn, may affect the price  of hazardous waste management services,
              the quantities of hazardous  waste  management services performed  on site and
              commercially,  the quantity  of other  inputs used on site and  commercially,
              and the  quantity  and price  of final  products produced.
                  The partial  equilibrium multimarket  model uses minimal   data about the
             markets  to project these market  adjustments.   The model uses  percentage
             changes  in production  costs  as a  result of the regulation to  generate the
             percentage changes in  the following market variables:
                  •    Price and quantity of goods  produced in each generating
                       sector
_
                                                 8-20

-------
     •    Quantity of hazardous  waste management  services  produced  and
          consumed,  on and off site,  for each  sector
     •    Price and quantity of  commercial  hazardous waste management
          services supplied.
     These results are used to calculate economic impacts  that  result from
the regulation.  A detailed description of  the model is presented in
Appendix I, Section 1.3. '
     To describe the relationships between  the sectors in  the affected
markets, a set of parameters—including the demand elasticities in  the
final products markets, the supply elasticities in the hazardous waste
management markets, and the share of total  production costs represented by
hazardous wastes—is used as presented in Section 8.1.
      In addition to the parameters already  developed, several other
parameters—dealing largely with each sector's share of the hazardous
wastes industries—are required to run the analytical model.  These "share"
parameters are shown in Table 8-7.  The values shown in column 2 of Table
8-7 are each generating sector's share of commercial hazardous wastes.
Similarly, columns 3 and 4 of Table 8-7 represent the other two parameters
(the  proportion of each sector's total demand for hazardous waste manage-
ment  services  supplied onsite and commercially).  The cost shift for the
marginal facility is the shift parameter.  Five shift parameters are used,
one for each control option.  These shift parameters, XI,  X2 , X3,  X4,  and
X5, are shown  in Table 8-8.
      Another set of parameters describes the relationship between inputs in
the production processes of each sector.  These parameters are the elas-
ticities of substitution between the  various inputs  used by the producers.
It is assumed  that the  production of  the goods produced by the generating
sectors involves the  use of two inputs.  These inputs are  (1) hazardous
waste management services,  and  (2) a  composite input.  The elasticity of
substitution between  these  inputs measures the ease  with which the producer
can  substitute between  them in his production process.  It  is difficult,
a  priori,  to tell  how much  substitution  is possible  between  hazardous waste
management services  and all other inputs—"waste minimization."  It is
assumed that some  substitution  is possible between  hazardous waste
                                    8-21

-------
    •- CO
    U  I
    0 CO
    £ k
    n r-I
4?
 n   >
 c  n
 o  0


— ">  i
 •  L.  is
    0  r-l
 o
CO
       c.
       o
      43
       u

      CO
                to  co  ^ ^  TH
                CM  S  r-l  CO

                CO     tO  ^~
                                 10  CM
                                            IDIO-rircOtOCOOQCO
                                                                           Q
                                                                           CQ
                s   CO
                CO O)  CO
                CO O)  O3
                                     O>
                                            O)0>OO)O)O)
                                                                       O>O>O>
                to  o
                                                                                  to
                          00
                          1-
                          0
                                 JB
                                 0
                                        -o
                                        C
                       CD
                       c

                      43
                   B  C
                   43 .-  ,
                   U  t.
                   3  0.



                   I  «
                   Q. 43

                   _  °  '

                   — -O

                   •i  2.

                   «  "•
                                 —     3
                                 •     0
                                 U
                                 •o

                                 i
    o
    L.
   43


    §.
                                 43


                                 0

                                 U
«

43

O
3


O
L
Q.
                                 l-
43  Q.




J1
                          c   e
                         j;  xi
                          u  —
                                 (*
                                ^
                                 Q.
                                     u«ue
                                       —  4»c—
                                       —  waa
                                       rs
                                       C  X
                  o  «  —
                 —  E  ^
                 43      o
                  e—   5
                  onE
                 —  o
43




I
Q.





I


C

O
L.

3
43

U
 01

_0

 a
 
                        —  L.   C ••-  —  O   0
                                                                                                      O  O  ~O
                                                                                                         O   0
                                                                                                         I 8^
                                                                                           a>
                                                                                           a
                                                                                           c
                                                                                           a
was
zardo
                                                                 O) —  O
                                                                    43  43
                                                                                  43  O)  II  0  —
                              —      II  43
                                         8-22

-------
Oe
UJ
a.
a:

i-

ui
CO

%
£
§3
co
 i
00

a
 X

JQ


 O

 49
 a
 o
                 CM
                 I
                           s>
                           u>
                             §!"•  1O  V
                                 1-4  t-l
                         «      CO
                                                       IN  iH  00  S  TH  S
                                                       ft  CO  U>  *  ft  •»
                                                                             s  s
                           U>      CM      i-l  O)      CM  ft  CO  5>  i-l
                                   CO      CO          "I  CO  UJ  ^  r-l
                                                                                                       flS  C^

                                                                                                       S>  i-«
                                   O>    O>
                                                                                               to  S  tO  CM
                                                                                               CO      •*•  Q
C^  IS  ^B  f^  LO  CO
S      CM  CO  i-l  O>
•V      CO  CO  CO
                                                       CMf-IOOS
                                                                  »-
                                                              f-CMIOi-l
                                   to  *T  CO  CD      tOCOUJT^fCM^-
                                                                                      CO  CO  tO  CM
                                                                                      s      *  §
                              c
                              (8
                              O)

                              O


                          c  c

                         3  •
                      «  c  u

                      o "L. 'c
                      3  a.  a
                     •o      o»
                      o   -  t.
                      t.no
                      a. -P  c
                          o —
                               ._   o  J,


                                .   *  s
                               _   u  —   01
                               —   0   E   t.
                               4>O.CC

                                C   O.  O  —
                      -o  0  a   -
                      c  u  —  at
                      »  3  t-  U
                  00      4>  4>  —
                  C  C  —  W  43
                 ,•-•  —can
                  c  to  u  -o  a
                  —  L.  3  C  —
                                                (I
                                                u
                                                o
                                                o
                             a
                             o
                             o

                            •o
                             c
                             a

                             E
                                                        o
                                                        t.
                                                       49
                    —   m   -
                     a   49  to
                     O   U  49
                    —   3  O

                     3   O  TJ
                     0   I-  O
                     U   O.  L.
                     a       o.

                     u   a  T3  o)  o)
                     a   o  c  o  c

                    "SL  'i  —  !5  'c
                         O  —  «i  a

                    —   U      —  E
                     a       -o  o-  o
                     o   -o  c      u
                         0  O  ..
                                                                                a.
                                                                                a.
                                                                                3
                                                                                n
                                                O)
                                                            U  -P
                                               —  n
        .1   £>!

     c  "5   c   i-
     o   a  —   0
    —   £  jc
 (0  49       U   C
—   •—go
 •   u   a   E  —
43  •—   l>      49
     St.  —  —   
 3   C
 O  —
 t-

49  J^

CM   0

 n  —

 E   u

 =   i

 8   I


 at    -
 t-  u>
 0
43  -C~
     fen


 ?   !
 a  .e
 a. 49

4>  fl
•f
—   m
JC   C
 0)   O
                      —   E
                       o   a.
                       u   a.
                      49

                       i  S
                       O  LO

                       c  i-T
     43
 49  C

 %  i

 v  &
 -p  a
 n  c



 t!
     «
 .-  i

 O  0)
 49  3
 U  O

 S  T
     a
 JC  N  CM
 O  (9
 O  .C  00

 *  0   c
 «t-  43   O

 °  "5  4>
 o  c   u
 —  00
 49      CO
 a  0
 I.  .C   C
     49  —

 £  o  -o
 49  49   0
—         c

 49       IS
 c  c  —
 coo.
 »  —   X

 2  -S.  •

 8- °   2
 t-  —   a
     o
 0  U  —
                                                                                                                      a.
                       i   s   a.
                      •o  s   a
                      ^t  Ift   r-
                       Ct      VJ
                           II
                      t-       C
                       O  CO  —

                       0  -o
                       in   c
                       3   a

                       0  01
                                                                                                                                                     0
                                                                                                                                                    .0
                                                                                                                       0  49 -O  C  TJ
                                                                                                                      -c  o.  «  o  o
                                                                                                                      H-  O 49  U  E
         L.
_       O
4»   •»  in
     in   0
 c   o  -o

 °   c   0
 X  0   I.
—   CD  a
49   L.
 C   O   M
 a       c


*E   O- 49
 o       a.
TJ  B>   o
 0

 ol  "   o
    i-t   t_
-O  ^ 49
 0       C
 
49   0

ft  ~  'i'

 »   5   S-
 0)   >   Q.
 C  *~
 O  «*-  S

49  49  S)
 O.  O    -
 O   0  CO

—  «^   II
 O   0
 I-   t-   LO
49
 c  -o  -o
 O   C   C
u   a  a
                                                                  8-23

-------
 management  services  and  all  other  inputs;  specifically,  all the
 elasticities  of  substitution are set  equal  to  1.
      In  summary,  the impact  model  is  a  system  of 82  linear equations
 representing  the activities  and relationships  embodied  in each of the
 affected markets in  terms of the parameters described above and the
 dependent variables.  These  dependent variables are  the  percentage changes
 in  prices and quantities in  each of two sets of markets:  the markets for
 goods  and the market for hazardous waste management  services.  This system
 of  linear equations  is represented by
                                  Zx = y
where
     Z - an 82 x 82 matrix of coefficients
     x s an 82 x 1 vector of percentage changes in the dependent variables,
         and
     y - an 82 x 1 vector of shifts in market relationships resulting from
         the control option.
To solve the system of equations, the Z matrix is inverted and multiplied
by the vector of shift variables:
                                 Z~l \I = Y
                                    y   A
For a more detailed description of the model, refer to Appendix I, Section
1.3.  This model is a simplification of a complex set of technical and
behavioral relationships.  It can provide only a general indication of the
types of pressures and adjustments that may result due to the costs of
complying with a control option.
8.3  ECONOMIC IMPACTS
     The increased cost of performing hazardous waste management services
due to the control  options will affect plants with TSDF in several ways.
Captive facilities use hazardous waste management as an input in the pro-
duction of their products—for example, industrial chemicals.  Managers of
these plants may elect either to incur the higher costs of onsite hazardous
waste management or to purchase these services from a commercial firm.
Commercial firms will experience increased costs of hazardous waste
                                    8-24

-------
management services.  This will affect the prices they charge for hazardous
waste management services.  Next, the impact of the regulation may be felt
in the markets for the goods and services produced by generators of hazard-
ous waste.  The partial equilibrium analytical model described above is
used to estimate the direction and possible magnitude of changes in the
following:
     •    Quantities of goods and services produced in the 20 generat-
          ing sectors
     •    Prices of goods and services produced in the 20 generating
          sectors
     •    Quantities of hazardous waste management services supplied
          by captive and commercial facilities
     •    Quantity of commercial hazardous waste management demanded
          by each of the 20 generating sectors
     •    Price of hazardous waste management services
     •    Quantity of organic air emissions.
The number of facilities affected by the control options are  identified in
Table 8-9.
8.3.1  Price and Quantity Adjustments
     Changes in the prices and quantities are projected for each control
option for each of two markets:
     •    The market for goods and services produced  by demanders  of
          hazardous waste management services
     •    The market for hazardous waste management services.
     Insignificant price  increases and quantity decreases are projected for
the products produced  by the 20  generating  sectors  (see Tables  8-10 and
8-11).  These adjustments are  expected to be  small  due to the minor share
of production costs represented  by hazardous  waste  management services.
Hazardous waste management costs represent  less than  one-tenth  of  one
percent of production  costs for  all  generator sectors except  plastics.
     Only slight  reductions are  projected in  the quantity of  hazardous
waste  generated under  all control  options.  These  reductions  are due to two
factors.  First,  the  reduced output  rate  of the 20  generating sectors will
                                     8-25

-------






a:
0
CO
H-


:
fl

 m
CM O
tH



tH CO
CO IS)
tH






CO CO




3 §
•"*

^«J cO
CO fH
tH





U
•—
C
a
en
L.
O

ca no
c c
49
c o
"Z "c
Q. a
o>
- u
n o
49 C
o —
•o -
o «
t. —
Q. a
t o
ll
0. U
?!•
a L.
49 49
• •» 0)
C 3
L n?
3 C
LL. JH
CO CO CO
CM fH CO




CO CO tH
CM i-i ir






to in in
CM tH CO




CO C0 tO
CM tH •»


C9 CO 10
CO tH ^-



n

m
u
••


JC
o

_>•
•
u
••»
•o
i
»
— 
o — 0
— en 49
49 O t»
•) — O
• on
— — n
Ct* CD ^
S 10 CO
•»•




•*• to co








*f tH




^ tH


CO CO S
Ul fH



_
a
o
u

•o
c
a

£
3
0
o
L.
a.


m
49
u
3
•o
O
t.
o.
0 U 0
— •> a
| * S
C 49
4) ,f} Q


« 3 O
u* QC O
CO tH 0) tH
f •» CM CM




o> u> CM co •»
T V tH CO CM







IO ^ tH CO CM




CO •» S •» CM


OJ tH ^ t— 1 LO
CO CO tH •» CM














U
0

O.
a.
3
> c c
<- a e
0 i
.E £.?
^03
coco-
.2 g 2 •
n -u o c
— a — a o
* o a E —
e 'u — — a
« 45 O L.
x «»- o — o
L. 0 t. O.
a ^ ™" 49 e)
E a 0 u c
•~ 49 c 0 a
t» 0 O ^^ t»
CL 2E Z LU ^
^ CO h- CM
tH




u> co h- co
fH







tH




co ^ r*" co
fH


co ^ i^** ^r
tH














0

a
n
0
0) .—
c m m
— 0 



to •q- 10
CM <9







5 1O
fH 1O



co •» r«-
CM •*
tH eo

CO *T *H
CM CO
fH to










n
0

49 10
'w 0
1. —
0 -o
> c
,_ fg
C -C
3
0
«r »
— a
a x
49
•- (0
Q. 3
« o
o -o
.C L.
a
» N
m a
_O JI
a 10
a a
j: — 49
u u o
t. t. H

0 p
10 E
0 0




0

43
0
4>

3
10
0


a
in
a
m
0
u

t_
0

49
i
0
0>
a
c
E

3
a

m
3
O
•o
L.
a
N
a

en
c

'i
o

L.
0
O.

o
49
10
O
U
TJ
S
a
u

0
.c

a


0

a cT
•o x
55
u c
0 0
>
L.
0 49
.C 10
1- 3
•o
C
• M
n
X f> 0
to a
^_ ^^ .^
a
t. — m
00 —
> TJ j:
0 O 49
10 2
c
C 49 —

S ~°
U. E O
Q «l •—
IO 10 <•-
•-85
49 M C
0 < 0
0 T3
«*. O .—
4: o
a u 0
3 L.
— o a
— CO
'* ^0 C
m 49
0 E .7
.— o
49 1. CM
a «t-
°^ Q
— 0 e
o c o
49 'a 49

O Ji 0
u o . a L.
— en a
49 L.
c o co
a c
CEO
*E O. 49
O CL
•0 Q O
0
L. II —
O. O
fH L.
•O >-/ 49
0 C
01 HI O
a — u
• -0 0
t- 0
0 49 —
L. C Q.
a 0 E
u a
to x
t- 0
.n o
en 0
3 10 -C
o — 1-
t. 0
49 0 •
tH 'i'
0 0.
ID > a
o «f- s
49 49 <9
a. o -
O 0 CO
— «»- ll
0 0
t- L. tO
49
C -O TJ
O C C
t> a a
ja
8-26

-------




Q
UJ
i^
•3
o
£t
a.
ul
O
M
i


S S> S  CO
CO CO O «^

51 S> O B



1^ O CO O>
CO 00 Q i-l

_T j^ » ,^
^" W Q« CS



0) •"•
O A O
— O O

<9 *E ~O
O) 9 C
f. J= «
o 0

Oft "V "™ ^
C C 9 0
— 9 O —
• 49 •_ o
3 .E 2 1 J;
0 t. c E 0
3 O. 9 Q.
•§ . ? - « .
I.MO 9 49 M
a. 49 c o o 49
o .- — 3 o
— 3 49 -D 3
— -O • 3 O -O
— 0 •> 0 L. 0
Ei-— o a. i.
a. 9 9 Q.
— I.— MI.9-OIAM O
— 0EI-9O0O0 —
49 a. 0 0 j; •.- — — — M 49
X 9JC^ O.E-49 C- 9
00.0— 0 — W 9 9 0
49 9 -O O. O E -O
C t. — M O -O C O 9
9 3 U O — 09 - X •*-
0» 4949—0)49 1.491.
CC— M4»Ot-490C0 —
— — C3«l— O C J3 0 g O
C 9 t- -O 9 O M — -O i— 49
— I.3C — — M930t.^
2ou.i-ia_m>
- 1.
0
Nonelectrical mach








































M
9

O.
CL
3
M
TJ
C
9
D
Electrical machine
























S

Q















OJ
C
49 t-
1 ^
E U
a. a
Transportation equ
Instruments
Mi seel laneous manu










































01
0
49
49
Electric and gas u





































(A
0

*49
M —
• t
a 0
M >
0 *C
— 3
9
m
0 M
O 9
-C 49
* 'a.
Nondurable goods:
Research labs, hos


0
_c
49

i.
O

0
-o

9
O
49

9
C
9
0
49
^


•o
0
49
(f
E

i*
to
0

M
0
U

Q.

0
.c

-c
M
0
C
9
Jl
U
0
49
1-4 49
5 I
L.
C 0.
9
5 -
0) 9
at 49
0
_l M
II Ic
* 9

B
M
49 49
C M
9 O
U U

M- C
•— O
C •••
0) 49
— O
M 3
C "O
— 0
0 k
9 *H
O
0 0
M 1.
9 9
« -=
t- 0)
U
•— o
c •
0 — CM
O E
— 00
L. 9
o. c
49 0
0 C —
1 0 49
t- <• O

t_ _ ^^
• a.
(ft 0 C
t. u —
o
49 IK -0
U 0 0
0 O C
M — —
> 9
0) U —
C 0 O.
— MX
49 0
9 49
U C 0
C i 9
0 0
0» CO —
9 0
S) C T3
CM 9 0
10-
49 49 9
M U
*BS
products produced
because hazardous
Data for the anal
M »>
"5 i.
u a.
49
C 5)
O Q
U U)
•,
C iH
o
*— 11

C •*. Ift
c 1 Si
? si
-0 <& 9
•o u> jr
9 U
II

O TO —
8-0 -o
C 0
D a -o
0 CM 't.
^ u
49 .. 0)
M 0
C O TJ
o •-•
C 0
X 9 L.
— O» 9
49 I.
COM
9 C
CEO
•~> o. *~
E a 49
o a.
T3 SI O
0
1. II —
a. o
<-• u
•O ^ 49
0 C
M M O
9—0
-0 0
U 0
9 0 E
O 9
ID X
<«- 0
.C O
CT> 0
D w x;
0 — 1-
1- 0
49 0 •
0 a.
M > a.
o <*- s
— K)
49 49 S
a. o
O 0 CO
o i "
t- t- ID
49
C TS T3
O C C
JU 9 9
8-27

-------



y
?N
^s
55
CL
CO
LU
£j
tJ
jj
fs
UJ
to


CO «
O fc
v? 3C
o o
Q£ S
u.
§tf\
pi
OU «<


fg» ul
oc o
•» III
jjj t_
8 JT
^^ *n
>. 5:
CO ^
P M
11

|
r*
f-4
1
00
UI










•O^
c
c
*"•
c
o
—
0
43
c
o









1











u>












CO









t-4














Sector
d to 04 r**
1*4 Q (3 ^
• • • •
(S Q} O O
1 1 t 1


IH 10 M r-
ft C3 Q CB

IS Is <9 (s
1 1 1 I


lO CO i-< TT

^H ^» (9 ^tf
1 1 I 1


»H ^H U> ^
C*l iH Q iH

1 1 1 1
u> co CD r-
gr-t Q i-l


1 1 1 I



W —
^ •
O  » O
• co -o L.
49 ._ ._ c 49
o i. c i c
3 o. a ex
"O 09 •*
o - t. —  o a 43 n
O. 49 C O O 49
o — — 3 o
— 3 49 -O 3
— -V - 3 O -O
— on c u o
e i- — o a. L.
Q. a a a
c o I — c
— u— n i. a -o n r) o
•— CELaoooii •—
49 0.1 f, 2 .-.-•-•- Bl 43
x a^^> Q. E — 49 c— a
• a. u — c — 01 a a o
49 «*-~^aaCL43 —
•* — — O — E * t-
-o c a -a -o a o £ J3
cu— OIOTJC oa
CC— 0>49Ot.490Ca —
— — C30i— oc^oea
cat--oao« — .0 i — 49
— t-3C — — « a D C 1- •




































Q.
Q.
3
01
-D 49
>> C C
S; • 1
Nonelectrical machin
Electrical machinery
Transportation equipi
Instruments






































C9
c
t.
49
O
Miscellaneous manufa






































01
0
49
3
81
0>
•D
C
a
u
't.
45
O
«
LLl




































a
01
9
holesal
Nondurable goods: wl



































01
0
49
ivers
c
3
01
"5.
01
O
j:
oT
.0
a
.c
o
L.
0
01
£
e
49
L.
0


<••
O
o
^
«H
a
u

49
X
a
c
a
0
-c
4»

•o
s
1
49
M
0

in
o
49

49
C
a
3
o-
j:
49
c
01
0
a
a
9
49
iH 01
S 49
? 1
c a
1 ^
j>
e) a
0) 49
_J 01
II J=
* a

49
C •
a 01
0 49
— in
«l- O
•- o
c
O) C
•~ o
0) •—
C 49
•- O
3
0 TJ
L. O
a i.
Q.
01
$ *s
a
2 2
u a
o -c
TJ 01
49 O
— C
"c 'i ^
a OD
3 a
o- c
49 O
9 C •—
-C ID 45
1- 01 O
O 0

in o c
L. «. —
O
49 01 TO
O 0 0
oil 1
C 0 O.
— 0>X
U 49 »
L C 0
001.
c i a
0 9
OJ O9 —
a 0
S C T)
CM a o
^ 0 -
49 49 a
0) 0
^. A .—
products produced b;
because hazardous w<
Data for the analyt

-£ e
O Q.
U O.

C B
o o
o to
C T*4
o
— II
(/> ij- 63

§*** U)
E
Q. L.
c a 0
O 49
| (^ f\
T3 to -C
a u
It

o co —
0 T> T3
0> C 0
3 a -o
9 CM 't.
-C O
49-01
0> 0
C O TJ
O —
C 0
x a t-
— 09 a
49 t.
c o «
a c

•^ Q. •••
§O. 49
Q.
T) O 0
t. II —
0. 0
tH I_
-0 v-/ 49
0 C
01 oi o
a — o
J3 O
t. 0
0 49 —
u c a
a o E
u> x
JC "S
o> 0
3 01 j:
Is"
49 0
"^ 0 Q.
01 > O.
O «t- S>
49 49 B
0. O -
0 0 CO
— t- II
O 0
U L. tO
49
C tJ T>
O C C
u a a
8-28

-------
reduce the generation of hazardous waste.   Also,  it is assumed that some
potential waste minimization will  further contribute to the reduced level
of hazardous waste generation.  The sector-by-sector values for all options
are shown in Tables 8-12 to 8-16.   Overall, the projected reduction in
hazardous waste generation is between approximately 200,000 and 800,000 Mg
annually, depending on the control option.
     The major adjustment projected is the shift to less offsite manage-
ment.  Although the price of offsite management services is projected to
increase only minimally for all control options,  these increases are more
than the cost increase for relatively large captive hazardous waste manage-
ment facilities.  Thus, the quantity of offsite hazardous waste management
is projected to decrease slightly, as shown in Table 8-17.
8.3.2  Regulatory Costs
     A direct cost incurred by TSDF as a result of the regulation is the
compliance cost.   Compliance costs are the costs of meeting the air emis-
sions control options.  For each facility, these costs will vary depending
on the configuration of the facility and the volume of throughput.   Tables
8-18 and 8-19 present the compliance costs without quantity adjustments and
with quantity adjustments presented above, respectively.  The compliance
costs are smaller with the quantity adjustments because  less hazardous
waste is projected to be generated due to  reductions  in  production of the
goods and services produced by each sector and due to increased waste mini-
mization.
     A large part of the compliance costs  incurred by TSDF is the capital
cost required to modify hazardous waste management units to comply with the
control  options.  The capital costs are shown  in Table 8-20.  In Table
8-21, the percentage of the hazardous waste management costs are repre-
sented by compliance cost for all captive  and  commercial facilities.  For
most sectors this is below 5 percent.
8.3.3  Emissions and Cost Effectiveness
     Organic air emissions will decrease  for the affected  facilities due to
two  factors:   (1) the control efficiencies of  each option, and  (2) the
reduction in hazardous waste  generation.
     Table 8-22 provides the  baseline  estimates of emissions and the
percentage reduction from these values.
                                    8-29

-------
     TABLE  8-12.
QUANTITY ADJUSTMENTS IN WASTE GENERATION AND MANAGEMENT
 BY GENERATING SECTOR:  CONTROL OPTION la
      Sector
                                HWM services,  103 Mg/yr

                              Onsite  Commercial    Total
Mining
Grain and textile mill products
Furniture, paper products, printing
Industrial chemicals, inorganic and organic
Plastics, fibers
Biological, pharmaceutical, medical chemicals
Assorted chemical products
Paint and allied products, petroleum and coal
Rubber, plastics
Cement companies
Primary metals
Metal fabrication
Nonelectrical machinery
Electrical machinery and supplies
Transportation equipment
Instruments
Miscellaneous manufacturing
Electric and gas utilities
Nondurable goods: wholesale sales
Research labs, hospitals, universities
Commercial hazardous waste handlers
Totals
-0.14
1.05
-0.16
-439.00
-325.00
-17.20
35.60
-39.50
-0.03
-0.14
-6.80
-3.92
-0.15
-0.09
-2.91
0.17
*
-0.18
-*
*
NA
-798.00
-0.28
-1.63
-0.02
-9.78
121.00
4.03
-129.00
9.54
*
-0.03
-2.33
-1.03
-0.05
-2.34
-0.58
-0.30
-1.23
-1.38
-0.27
*
-15.80
NA
-0.42
-0.58
-0.18
-449.00
-204.00
-13.20
-93.80
-30.00
-0.02
-0.17
-9.13
-4.95
-0.20
-2.43
-3.49
-0.14
-1.23
-1.56
-0.27
*
-15.80
-830. 57b
* - Absolute value less than 0.01.
HWM = Hazardous waste management.
NA s Not applicable.

aData for this table are obtained from the Source Assessment Model (SAM)
 Industry Profile data base, (Appendix D, Section p. 2.1.), and from the
 analytical model (as explained in Section 8.2).
     effects of control option 1 on the quantity of waste management ser-
 vices demanded by the 20 generating sectors estimated by the analytical
 model are presented in this table.  Control options 1 through 5 are based
 predominantly on the use of add-on emission controls and reflect five
 levels of controls (1=0 ppm organ ics; 2 and 3 = 500 ppm; 4 = 1,500 ppm;
 and 5 s 3,000 ppm).  The example control options are described in
 Chapter 5.0.
                                    8-30

-------
   TABLE 8-13.  QUANTITY ADJUSTMENTS  IN WASTE GENERATION AND MANAGEMENT
                  BY GENERATING  SECTOR:  CONTROL OPTION 2a
HWM services, 10-
Sector
Mining
Grain and textile mill products
Furniture, paper products, printing
Industrial chemicals, inorganic and organic
Plastics, fibers
Biological, pharmaceutical, medical chemicals
Assorted chemical products
Paint and allied products, petroleum and coal
Rubber, plastics
Cement companies
Primary metals
Metal fabrication
Nonelectrical machinery
Electrical machinery and supplies
Transportation equipment
Instruments
Miscellaneous manufacturing
Electric and gas utilities
Nondurable goods: wholesale sales
Research labs, hospitals, universities
Commercial hazardous waste handlers
Onsite
-0.18
0.87
-0.17
-341.00
-326.00
-2.33
29.40
-4.71
-0.03
-0.15
-6.99
-0.94
-0.15
-0.09
-2.90
0.14
*
-0.22
*
*
NA
Commercial
-0.17
-1.35
0.02
-29.20
157.00
-8.57
-107.00
-20.10
0.01
0.01
-0.55
-3.16
-0.01
-1.91
0.01
-0.25
-1.02
-1.06
-0.22
*
-17.00
5 Mg/yr
Total
-0.35
-0.48
-0.15
-370.00
-168.00
-10.90
-77.50
-24.80
-0.02
-0.14
-7.54
-4.09
-0.16
-2.01
-2.89
-0.11
-1.02
-1.28
-0.22
*
-17.00
     Totals
-656.00
NA   -690.00b
* = Absolute value less than 0.01.
HWM = Hazardous waste management.
NA = Not applicable.

aData for this table are obtained from the Source Assessment Model (SAM)
 Industry Profile data base, (Appendix D, Section D.2.I.), and from the
 analytical model (as explained in Section 8.2).

bThe effects of control option 2 on the quantity of waste management ser-
 vices demanded by the 20 generating sectors estimated by the analytical
 model are presented in this table.  Control options 1 through 5 are based
 predominantly on the use of add-on emission controls and reflect five
 levels of controls (1 = 0 ppm organics; 2 and 3 = 500 ppm; 4 = 1,500 ppm;
 and 5 = 3,000 ppm).  The example control options are described in
 Chapter 5.0.
                                    8-31

-------
     TABLE 8-14.
QUANTITY ADJUSTMENTS IN WASTE GENERATION AND MANAGEMENT
 BY GENERATING SECTOR:  CONTROL OPTION 3a
      Sector
                                HWM services,  103 Mg/yr

                              Onsite  Commercial    Total
Mining
Grain and textile mill products
Furniture, paper products, printing
Industrial chemicals, inorganic and organic
Plastics, fibers
Biological, pharmaceutical / medical chemicals
Assorted chemical products
Paint and allied products, petroleum and coal
Rubber, plastics
Cement companies
Primary metals
Metal fabrication
Nonelectrical machinery
Electrical machinery and supplies
Transportation equipment
Instruments
Miscellaneous manufacturing
Electric and gas utilities
Nondurable goods: wholesale sales
Research labs, hospitals, universities
Commercial hazardous waste handlers
-0.32
0.23
-0.02
-97.60
-47.90
-2.04
7.74
-6.41
*
*
-7.66
-0.94
-0.02
-0.06
-0.54
0.04
*
-0.168
*
*
NA
0.23
-0.36
-0.02
0.05
3.54
-0.83
-28.10
-0.12
-0.00
-0.34
5.67
-0.14
-0.02
-0.47
-0.22
-0.07
-0.27
-0.17
-0.06
*
-21.40
-0.09
-0.13
-0.04
-97.60
-44.40
-2.87
-20.40
-6.53
*
-0.04
-1.99
-1.08
-0.04
-0.53
-0.76
-0.03
-0.27
-0.34
-0.06
*
-21.40
     Totals
                             -156.00
NA   -199.00b
* - Absolute value less than 0.01.
HWM - Hazardous waste management.
NA s Not applicable.

aData for this table are obtained from the Source Assessment Model (SAM)
 Industry Profile data base, (Appendix D, Section D.2.I.), and from the
 analytical model (as explained in Section 8.2).

"The effects of control option 3 on the quantity of waste management ser-
 vices demanded by the 20 generating sectors estimated by the analytical
 model are presented in this table.  Control options 1 through 5 are based
 predominantly on the use of add-on emission controls and reflect five
 levels of controls (1=0 ppm organics; .2 and 3 = 500 ppm; 4 = 1,500 ppm;
 and 15 = 3,000 ppm).
 Chapter 5.0.
     The example control options are described in
                                    8-32

-------
    TABLE 8-15.   QUANTITY  ADJUSTMENTS  IN WASTE GENERATION  AND MANAGEMENT
                  BY  GENERATING  SECTOR:   CONTROL OPTION 4*


                                                 HWM services,  103 Mg/yr

     Sector                                    Onsite  Commercial    Total
Mining
Grain and textile mill products
Furniture, paper products, printing
Industrial chemicals, inorganic and organic
Plastics, fibers
Biological, pharmaceutical, medical chemicals
Assorted chemical products
Paint and allied products, petroleum and coal
Rubber, plastics
Cement companies
Primary metals
Metal fabrication
Nonelectrical machinery
Electrical machinery and supplies
Transportation equipment
Instruments
Miscellaneous manufacturing
Electric and gas utilities
Nondurable goods: wholesale sales
Research labs, hospitals, universities
Commercial hazardous waste handlers
Totals
0.05
0.44
-0.20
11.40
-328.00
-2.47
15.00
-6.62
-0.03
-0.18
-7.44
-1.10
-0.16
0.48
-2.99
0.07
*
-0.32
*
*
NA
-323.00
-0.23
-0.69
0.13
-200.00
243.00
-3.08
-54.40
-6.00
0.02
0.11
3.60
-0.99
0.07
-1.51
1.52
-0.13
-0.52
-0.33
-0.11
*
-199.00
NA
-0.18
-0.24
-0.08
-189.00
-85.80
-5.55
-39.40
-12.60
-0.01
-0.07
-3.84
-2.08
-0.08
-1.02
-1.47
-0.06
-0.52
-0.65
-0.11
*
-19.90
-362. 00b
* = Absolute value less than 0.01.
HWM = Hazardous waste management.
NA = Not applicable.

aData for this table are obtained from the Source Assessment Model (SAM)
 Industry Profile data base, (Appendix D, Section D.2.I.), and from the
 analytical model (as explained in Section 8.2).

bThe effects of control option 4 on the quantity of waste management ser-
 vices demanded by the 20 generating sectors estimated by the analytical
 model are presented in this table.  Control options 1 through 5 are based
 predominantly on the use of add-on emission controls and reflect five
 levels of controls (1=0 ppm organics; 2 and 3 = 500 ppm; 4 = 1,500 ppm;
 and 15 = 3,000 ppm).  The example control options are described in
 Chapter 5.0.
                                    8-33

-------
    TABLE  8-16.
QUANTITY ADJUSTMENTS IN WASTE GENERATION AND MANAGEMENT
 BY GENERATING SECTOR:   CONTROL OPTION 5a
     Sector
                                HWM services, 103 Mq/yr

                              Onsite  Commercial   Total
Mining
Grain and textile mill products
Furniture, paper products, printing
Industrial chemicals, inorganic and organic
Plastics, fibers
Biological, pharmaceutical, medical chemicals
Assorted chemical products
Paint and allied products, petroleum and coal
Rubber, plastics
Cement companies
Primary metals
Metal fabrication
Nonelectrical machinery
Electrical machinery and supplies
Transportation equipment
Instruments
Miscellaneous manufacturing
Electric and gas utilities
Nondurable goods: wholesale sales
Research labs, hospitals, universities
Commercial hazardous waste handlers
0.05
0.44
-0.20
11.30
-329.00
-0.26
14.80
-6.63
-0.03
-0.18
-7.44
-1.10
-0.16
0.48
-2.99
0.07
*
0.11
*
*
NA
-0.23
-0.68
0.13
-190.00
243.00
-5.26
-54.00
-5.90
0.02
0.11
3.62
-0.97
0.08
-1.50
1.53
-0.13
-0.52
-0.76
-0.11
*
-19.90
-0.18
-0.24
-0.08
-187.00
-85.20
-5.51
-39.20
-12.50
-0.01
-0.07
-3.81
-2.07
-0.08
-1.01
-1.46
-0.06
-0.52
-0.65
-0.11
*
-19.90
     Totals


* = Absolute value less than 0.01.
HWM = Hazardous waste management.
NA = Not applicable.
                             -320.000
                                                            NA   -360. 00b
    effects of control option 5 on the quantity of waste management ser-
vices demanded by the 20 generating sectors estimated by the analytical
model are presented in this table.  Control options 1 through 5 are based
predominantly on the use of add-on emission controls and reflect five
levels of controls (1=0 ppm organ ics; 2 and 3 = 500 ppm; 4 = 1,500 ppm;
and 15 = 3,000 ppm).  The example control options are described in
Chapter 5.0.
                                   8-34

-------
        TABLE 8-17.   PRICE AND QUANTITY ADJUSTMENTS IN THE MARKET FOR
               COMMERCIAL HAZARDOUS WASTE MANAGEMENT SERVICES3

Control15
option
Baseline
Option 1
Option 2
Option 3
Option 4
Option 5

Waste quantity,
103 Mg/yr
5,718
5,703
5,702
5,697
5,699
5,699

Price of HWM,
$/Mg
1,276
1,281
1,280
1,277
1,278
1,278
Change from

Quantity
._
-0.28
-0.30
-0.37
-0.35
-0.35
baseline, %

Price
«, «•
0.44
0.37
0.10
0.19
0.19
HWM = Hazardous waste management.

aThis table presents the changes in the prices and quantities estimated by
 the analytical model for the commercial hazardous waste management sector.
 The price increases and quantity decreases are small in comparison to the
 baseline price ($l,276/Mg) and baseline volume of hazardous waste services
 supplied (5.7 million Mg).  Data for this table are obtained from the
 Source Assessment Model (SAM) Industry Profile data base, (Appendix D,
 Section D.2.I.), and from the analytical model (as explained in
 Section 8.2).

^Control options 1 through 5 are based predominantly on the use of add-on
 emission controls and reflect five levels of controls  (1=0 ppm organics;
 2 and 3 = 500 ppm; 4 = 1,500 ppm; and 5 = 3,000 ppm).  The example control
 options are described in Chapter 5.0.
                                    8-35

-------
H
t_
>•
ffl^
%
*>
•»
CO

rl
HI
3
Q
3
g

3
&
.
CT
•HE
5?
g
i
t^
p
s"
0
1
0
u
>.
ffi

J2
•18. COMPLIANCE COS!
CO
iu
)-






JO
c
G
4>
Q
O
"o
-p
§
,3
*M*





















LO




^^



CO


w





vt













t.
o
u
r*. r*.
Q 0)
® o



R J*»
rH CO
O Q


B rH
B B

B S-
rH OS
B B




OS h.
rH 0)
B B











4>
•o
O
L.
CL
'i
9
4>
X
TJ
C
c c
"c "«
3 0
CslQOJO>COf'^COCDiHQ
rHQCMLOCOr-IISQQf-tQQlSkrHlS&QO
QOQr^r-ICMCQI&QCOQQOJQ&Q&tSQ
*H W CO
f*4

t*-QQ^"C&«-*SlT-lr-tr*-iHU>CDf11»»COr-l«-iea
rHrSJcoioOJCMQGli-ir'-iHCMQ.-tiHCVJQSl
c&oo^Hr-i^c')c&(&^(soo4G>is>Q&>c»>B;>
00 CJ CO
rH
^TjaQCMlSlOOrHTj-O ^ «O M 00 CO & O1 *-4 5>
Q€9)C)>N>lOO>&QCSlrOQCO*S)1S)Q)r4Qr-4COe>Ii-4i-1CSlQQ
^3 CO s rH QO *^ ^3 B 40 B IS C4 B IS ^d B B B
B CM CO
C*. ^r


^&BCOBBi-4rHCMh*COrHr-|^cOCMCMB
••4BBr-BBBCMCO- -c a (A
oo S
c •—
e 1? "Z « •**
c c a o CA —
•- a o - n o M
«** "^ O €) ^— L
c o -a L .= ra «
T B I « a « >
Q. a Q. a. o c
» ? a" 4? « S " » • =
n o a 4^ n •— c to -
-PC U O -P T3 -P I- .- S W
S ~ 3 •§ S ? S I 5S-5-5
i • §n ?xi s^ii
C.— UCLL. •— !.•— c».4» Q.
°- « • CL -C « 3 33 n
e°..e"^^-- coccr c -0
t-*~*)t>.aTjtAn o a •— 9 atAto^c
cguauvu« — 6 ^ la-S
a. 9 9 jc — — — — « 4> u c So -
• JijaaE — 4>c— a— So not)
Q. o — c— « a a o a e •- 3 -o ra ^
. _ *- _r -g • • fr -8 T JJ - -8 5 8S °-2
0 a -a TJQ.oE^(.a4>cc —
U.-WOTJC o (0-POL.oauja-c
3 u o — c a « x<4-u— OE — .-a«3
4>4».-0)4> U 4» 1. C L. 0. 3 — t-St.
— »14»Ol.4>«Ca — — -P (A L. O 4J 3 (B
F-22T°c-niE<'«oc*>«o'o«
u-oaon — j3g.-4>coaMe)«c«
3c — — na3OL.co— L. c — — o co
u.rHCLca
rH









0)
9
izardous waste hand 1
m
Commercil
§
^J
CO
rH

§
rH

CM
B
B
to
to
CO

i
LO
CO
«0


§
CM
CO
CO











•5
*
•n
9
je
L.
g
rH
CM
9
4>
X
J3
O
Ji
O.
o
o
L.
4>
O
u
X
L.
O
H3
a
3
£

j;
O
a
0

«f-
o
4>
M
Q
U

0
U
C
a
"a
u
1

U
0


«••
a
"o
L.
o
u
IH

•o
c
a
generating sectors
B
CM-
sectors
0
u
L.
3
O
00

JC
E
o
L.

a


•
u
o
-p
u
0
(A
0
-p
C
TJ
0
TJ
3
"o
n
45
"o







.
rH
CM
Q
C
O
'-p
o
0
CO
o
X
•_
TJ
C
0
O.
CL
"*__
a
n
a
.a
a
4>
a
T3
0
«r-
o
L.
0.
X
L.
4>
3
TJ
C
M
_
"0
TJ
O
-P
(A
0)
(A
» E-
O Q.
L. OL

1 1

C rH
0
•- II
in •

i B a.
TJ B a
-o to .c
a u
ll
«•- c
O CO —
0 TJ TJ
ID C 0
3 a .a

« M 'H
-C U

uT 0
C U TJ
C 0
x a L.
. — o» a
4> L.
c o in
a c
c £ o
*1 CL 4>
0 OL
TJ B 0
0
t. II —
CL 0
rH L.
"0 ^ "c
(A (A O
a — o
JO O
L. 0
0 H* —
L. C Q.
a o E
o a
to x
<*- 0
-§, ° 0
3 m j:
o — H
L. 0
JC >
rH ~ 'i'
0 0.
«l > QL
c —
O «r- B
4> 4> B
CL U -s
O 0 CO
-5-S »
L. L. LO
C TJ TJ
O C C
u a a
8-36

-------


(9
C
X
CD

fH
W

(X)
^r


u.
55
3
O
it
t-H

1
«•

jE
1*4
S

1-4
|—
Q.
Q

«J
O

f™
z

o

v
£

en
fc
o
u
UJ
£
HC
M
_I
Q.
z
o

rH

00
UJ
m
<
P















_£
C
Q

49
O,
o
"o
49
o




















































10





- ^1"






CO




W





t«t































t_
S
u
0
(/>






s «
S 0




S h-
rH 
S 19





S 2
O Q



OD P""*
i*4 09)
Q O




O> h»
<3j i^


















40
O
•3
TJ
O
L,
CL

^_

,_
E
0

(_
49
X
^
C
•
o>
c c

'c "a
— L,
z o


rH 1
<9 O>
rH
tH



h. S
tH S
S 00
00
tH



S CO
d* QO
to



fSi ijjj
rH S
(9 CM
19
CM


5 1
t9 "f

CM






U

c
a

L,
o

C» TJ
c c
— a
49
c u
Is
o»
M O
49 C
O —

TJ ~
O M
i. —
CL (S
u
L. —
0 E
CL 0
• -C
CL U
0* a
L. • •
3 V.
49 49

C 3
U T>
3 C
U. HI


CO
rH
CM




CO
tH
rH
CM




§
u>
10
CM


(9
00
rH
"»•


1
CO

^


























IA
C.
0
-O
^
w
u

49
(A
a
CL-


IO
rH




U>
rH





CM
S



UJ
rH




UJ
IN.
rH






IA.

£
u

*ij
0
jc


a
o
TJ
^
(Q
U

49

0
U

L,
•

o.
—
u


Q-
vw
0
CD


§^SrH^CMO)CO^>COCOl9rH(9l9
rHC9Bl9rHBCNII9rHOI9OSO>
CMCOt9QcoO(9cNQ(9(9Q5>l9CM
CO tH




QSSrHCntOrHlOOOC-COrHrHSIS
CMCM<9SSb-tHCMC9rHrHCMSSC9
CMCO<9S^<9&CM<9<9<5><9<9C9CO
CO tH




I900rH^t9^COCMOOCO<9C^rHt9(9
U9O)S9CMrHrHCOCMt«-COrHrH<9&
^•tHt9rHCOOOrHCQCMrHrHCMe9<9h*OOrH^>r*»COCMCMt9t9
<9<9CM^COrHTfCOiHrHCMC9S(9
10CM<9<9COrHSCMt9S<9S
ID tH rH
tH




^
a
o
u

v>
c
a CA
0
E •-
3 49 (A
0 10 — L.
— CA 0 « 0
O 0 — i_ —
L — a 0 TJ
49 — 0) > C
0 CL —eg
CL CL 0 c j=
3 0—3
0) . CA c CA eg 0
49 W — 0 CA « 49
O49 TJ49 f_ .- 0 « CA
3O XCC 3 49 — — O
TJ3 L. O CD 49 — O R) ¥
O T> 0 E O — -C 43
L, o cxo. a — t — m
CL L, .- L. — 


<9
w
rH



§
T-4
f««
CM



§
LO
CO


1
rH
a>
CO


i
CO
m
00





























(A
eg
49
o
l-




L,
49 O
0 
c E D) u 0
O O — C CA
— o jc o eg
49 49 — J3
/> A •>«•
o -c c CL a
49 — E 49
— o eg
O DUTJ O TJ
t. C 0
49 — 49 C 0
c E c o —
O E 0 •-
U 3 (A Q *|
O 0 49 o
X L, 10 L.
<- X O-O O.
0 JO
49 «l X
a ,-N 49 • L.
— U CA — 49
3 O O 0 IA
O) i? o ~Q 3
0 U 0 TJ
L. 0 0 E C
CA U M

o — a a *-*


U 0.49 CO
«»- i- E x*-'
000 —
i O 8 —
u) 6 c 0
49 o 0 a TJ
(A O .C 0
0 r- 0 S
U rH JC

0 TJ • C
O C «. X 0
C O O -O E
a 49 CA
— IA U TJ CA
— 1. 0 0 0
CL O « 49 CA
E 49 3 CA
o 0 0 E <
O 0 JC —
0) 49 49 0
0 CA U
J= O9 C 0 U
49 C — 3
— IA O
CA 49 TJ 0 M
49 a 0 OJ
§U TJ C 0
0 3 a j=
 40 a 0
49 t_ — 3 C
o — cr—
IA 49 — a
— O U 0 49
jc 0 a jc ja
r- IA «t- 49 O
a

























































•
rH
CM
Q
C
O

49
O
CO



o o.
L, CL .
49


U IO

C rH
.2 i,
w
in T S

E ••« u>
0 E
Q. 1.
O 49
TJ (9 a
TJ U> JC
a u
ll
t- c
O CO —
0-0 -o
IA C 0
3 a -Q

0 CM L,
-c u
49 •- CA
CA 0
C O TJ
X ffl 1-
— o» a
49 U
C O CA
a c
CEO
***• CL****
§0.49
CL
TJ S O

1- 11 —
0. 0
rH U
TJ '-'49
0 C
CA (A O
a — o
ja o
t- 0
0 49 —
t- C CL
a o E
UJ X

49 0 •
™~ S*^
rH E
0 CL
0» > CL
C •"
o «t- a
49 49 (9
CL U •
O 0 CO
^~ *H II
O 0
t_ L, IO
49
C TJ TJ
O C C
u a a
ja
8-37

-------
                  goo
                  O)

              Q  rH
              O>  CO
              CM  OS
JO
 C
 o
 u
              IS  rH
              rH  10
                             co
                             CO
      CM
              O)  CO
              CM  O>
              S  rH
f  00
•»  OS
                                                                                        8    §
                                                                                              to
                                                                                              S
              CO rH
                         10  Q
                         U

                         'c
                         •
                         09

                         O
                                                                           *    §

                                                                                CM
tor
S
       49  "

   S  .5  .2
    o   t-  c
    3   O. •

   I   . ?
    L.   «  o
    a. 49  c
        o  •—
   —   3
   —  t>   •

   'i   2  —

    0   a 5
                 49
                  X

                 49
c   i.  —  n
•   3  L.  U
              c  c —  a

                     (. -a
                          e
                          o
                          u

                          •a
                          c
                                        s
                                       49
                                        U
                                                              g
                                                              a.
                                                              3
                                                              n
                       49  1ft
                    n  —  t-
                   _0  (A _0

                    IB  0 TJ
                    IA  >  C
                       —  a
                    C  c .c
                                                                         .5  g
                                                           f
                                                                             49 —  —  B
                                                                                     a 3
                                                                                     0)  O
                                                                         E«-o
                                0 Tl
                                —  0
                                         «4J
                                        «l-  0
                                             C
 oc90
—  ol  —  •-
                                                                             0J3j:.-
                                       —  JO
                                        K3
                                                                  0.3
                                                                  01l.
                                                    aw
                                                    UC
ot
                                                                         04»3
            mccinS
           —  —  OOO
                                                                                          IB
                                                                                          I-  0
                                                                                          0 JC
                                                                                          C 49
                                                                                          0
                                                                                          CD  C
                                                                                          CM T3

                                                                                             •O
                                                                                          IA  3
                                                                                          L. —
                                                                                          O  U
                                                                                          49  C
                                                                                          O —
                                                                                          0
                                                                                          IA  m

                                                                                          49 .2
                                                                                          0 49

                                                                                          t_ —
                                                                                          IB —
                                                                                          E  U
                                                                                              IB
                                                                                          rH H-
                                                                                          CM
                                                                                              IA
                                                                                             49
                                                                                              m
                                                                                              o
                                                                                              u
                                          o —
                                          —  IB

                                          ex. .—
                                          o  a.
                                              IB
                                          —  o

                                          e  0
                                          49  U
                                          B  C
                                          O  9
                                          O —
                                                                                                               IB
                                                                                                               49
                                                                                                               IB
                                                                                                               •o
                                                                                                               49
                                          o  i
                                          49  U

                                          —  0
                                          3 j:


                                          ?  »
                                          I-  O>
                                                                                      u  g
                                                                                      IB  E
                                                                                      0  3
                                                                                          O

                                                                                      O  X
                                                                                         .0
                                                                                      IA

                                                                                      in T"
                                                                                      o  o
                                                                                      O 49
                                                                                          o
                                                                                              8

                                                                                             I
                                                                                                       _»  * jj
                                          o  'o
                                              o

                                         S   °
                                          C  rH
                                          0
                                          (A  TJ
 a

 •  k
3  .8
 •  u

t  8
•-  O)
.c  c
9
    CM


 8  ^
    C
—  O


5  '-8
*CL  0
 IB  CO
 U


 §  °"
    X

49  T)
 IB  C

°  1
    a.




I  I"
 0    £L ^O

 .c  » 't-
  O)      U
  3  II   (A
  O      0
  I.  rH T>

 49      O
     _»  U

     O
  a  L.  in
  C  49  C
  o  c  o

 49  8 49
  o.      a
  O    C
  O  0  O
 o  —  o
J3
                                                        8-38

-------
       U>     Vf  00  CM  «  tH  CM

              Q  CM  CM  «H  IS  TH










J3            S  CM
  C
  o


  a
  o           CM  o>
       CO     CO  CM

  o           s

 49
  c


              OOI»-THUJB>U>COODtrflOCMtp«OCMg>lOUJOD??l1-S»
       CM     O>TH«OO>CMtaCM

              THCMCOCMCMTHTHU>rH*rr»CMCO^l5(CMCOCMiac3
                           CD
    09  -O
    C  C
    ._  9


 0)  C  O
49  .-  .-
 U  I.  C
 3  a.  9

 o   -  t-
 (_  9t  O
 O. 49  C
                   •i  2  •
                       Q.  9
                    9      U
4!  *
 X
                                   o
                                  .—
                                  -o
                                          -o
                                           C
                                           9
                                           a.
                           E
                        a.  o
                        »  ^
                        Q.  O
               —  3   O
               49 -O   3
                3  O  -O
                9  t   O
                O  Q.  t.
                9      O.
                                   nucu
Q.


3
IA



C
                       n
                       9

                       49   01

                       '«  _9
                                                                      0)


                                                                      _9


                                                                  01  9
                                                   (»      o
                                                   o      —
                                                              «
                                                              c
                   .—  .—  .—  .—   in
                    E  —
                    O—
     C  I.  —
     931.
 CO     49  49
 C   C  —  0)


'c  '9  i.  -o


3  O  U.  M
                                  —  o      —
                                -  »     -oQ-
                               BU-OC
                               O —  C   <•    -
                               .-  O)  -P       C.
                                                          O
                                                          —
                                                          i.
i
Q.

3

8*
c
o
                                                              — —   «-P
                                       «l.  O  •-
                                           •  1.
                               O.o3
                                                                  —
                                                               oj
                                                              •-   •
                                                                                 —   O
                                                                                 UJz
                                                                           .5
                                                                          t)   (A

                                                                          »   i
                                                                          49
                                                                          —   (A
                                                                          O.  3
                                                                          n   o
                                                                         .
                                                                              2
                                                                           ~  N
                                                                          wn
                       O  O
                       U  L.
                       caC
                                                                      DO
                                                                      acu
                                                                                   01

                                                                                   —      O)
                                                                                   Q.      C

                                                                                   —     49
                                                                                   a  9   9
                                                                                   49  49   t.
                                                                                   —  0)   «
                                                                                   a.  n   c
                                                                                   9  *   »
                                                                                   O      O)
                                                                                       0

                                                                                   •8  i  a
                                                                                   N  IA  ^
                                                                                   —  C
                                                                                   —  O   
                                                                                   a      t.
                                                                                   390
                                                                                   C  JC  49
                                                                                   C  49   U
                                                                                   9      0
                                                                                   ^  ««-   0)


                                                                                   3  »  «
                                                                                   01  49  JC
                                                                                   O  0)   L.
                                                                                   U  O   9

                                                                                   9  °   §
                                                                                   O  49   iH
                                                                                   C  C   CM

                                                                                   .2  I   .
                                                                                   —  9  -C
                                                                                   Q.  O)  49

                                                                                   I  3  ^
                                                                                   U  9   O
                                               5  o
                                                n   x
                                                o  —
                                                o  -o
                                                    c
                                                9   o
                                                u   a.
                                                c   a.
                                                a  <
                                                a.  9
                                                E   01
                                                o   a
                                                U  -JO
                                                a  -o
                                               49
                                                a   0
                                               a  —
                                                 •   o

                                               "u" a.

                                               5   »
                                                u   u
                                                   84>
                                                    0)

                                               4>  -O
                                                C   C
                                                                                       f-\  01
                                                                                       49  a

                                                                                        9
                                                                                        U  0)
                                                                                        U  3
                                                                                        «  o
                                                                                        a.  -o

                                                                                           a
                                                                                        c  N
                                                                                        o  a
                                                                                    o   9
                                                                                    a.  3
                                                                                    o   c
                                                                                    u   c
                                                                                    a.  9

                                                                                    9   e
                                                                                   j=  j=
                                                                                    n   o
                                                                                   49  49
 01  IA
 O  4>
 t-  n

 a 8

—  O)
JB  c
 e  —
4>  49
    9

.2  *
jc  a.
I-  o
 o  o>
 9  a
 e  c

 t.  E
 o
 <•-  «
     49
 "O  0»
 c  a
• a  i

 c  IA

 -2  g
 49  -O
 a. u
 o  a
     N
 —  te
 o  -c
 L.
 49  —
 C  9
 O  •-
 U  U
     t_

 o  1
 a  E
 e  o
     u

 O  TH
 «»-
     -o
 4>  C
 c  a

 i  «.
 «  t-
 co o
 a  4>
 c  u

 i  Z
                                                                                                                      49
                                                                                                                      C
 8
 t_

 o
CO

 o

49


 |

«t-

-o
 «
                                                                                                               ti
                                                                                                                i.   a.
                                                                                                               4>
                                                                                                                C  ^
                                                                                                                o  o
                                                                                                                u  u>
                                                                                                               —   II
                                                                                                                IA
                                                                                                                IA  ^-
                                                                                                                C  »-i tA

                                                                                                                i  E
                                                                                                                    CL  t.
                                                                                                                C  Q.  «

                                                                                                                        Q.
                                                             O


                                                             4  1
                                                                                                       C
                                                                                                       o


                                                                                                   *9  49
                                                                                                   49  U


                                                                                                    O  CO
                                                                                                                -O  1O  JC
                                                                                                                9     (J
                                                                                                                    II
                                                                                                                <<-      C
                                                                                                                O  (O  —

                                                                                                                    S-o  -o
                                                                                                                    C   9
                                                                                                                3  9  -O


                                                                                                                1  "   b
                                                                                                                49  •«  0>
                                                                                                                    0)   9
                                                                                                                c  o  -o

                                                                                                                    C   9
                                                                                                                >,  en   t.

                                                                                                                49  L.
                                                                                                                C  O   01
                                                                                                                9      C
                         E  Q. 49
                         o      a.
                         -o  B  o

                         £  „ -
                         Q.      O
                             iH  I.

                         •O  V •*

                         0)  IA  O
                         9  —  O
                         JO  O
                             t-  9
                         9  49 —
                         I.  C  Q.
                         9  O  E
                             u  a
                         U)      X
                             *t-  9
                         -C  O
                         CO      9
                         3  l» J=
                         O  — r-
                         (.  9

                         49  9
                                                          4> 49  (9
                                                          a.  u    -
                                                          o  9  co

                                                          — "^   II  '
                                                          O  9

                                                          49
                                                          C -O  TJ
                                                          O  C   C
                                                          una
                                                         J3
                                                             8-39

-------





rH








O CM
P .Q
§5 a
c
_l o
a •-
K 49
r— a
z o
^3
O CO
>• L.
CQ 4^
c
 o
a °
*^\
tu
M
I***
o ^c
LlJ
UU
LL>
LU
H
O
tj
§ to
^

2?
o
s
C/) 1

§


•
CM
CM
1
CO
111
_J
CD
£













tH
tH
tH








CO
rH
rH






^
^sf
rH





CO
10
rH








rH
CO
rH















O
C.
9t
•51
2
CO

rH

M
C
O
M
n
H


s>
CO

.
rH






S
10
i-T





S
CM
X
rH




CO
^f
.
rH






S
CO
CO
.
rH











y"\
0
C
0
TJ I)
J-8
'•P E


•D «r-
t_ t.
C -^
O CO
a
o) co
5S
rH
CO
00
00 IS
CO







00
rH •
CO IS
CO




IO
CM

IO S
CO



CO
rH
rH •
r- B
CM






^f
rH
CO 8
rH











0
^^ ^^
e c
a> o
a >—
t- 4>
0 U
> 3
« -o
>"— ' fi
L
(A
en c
0 o
4> C —
w 0 w
o > «
u *~ >^
4> E
0 U 0
00 0
C X-> «^
(A 1
rH C O 4> ^-v
• O T3 (A CO
00 •- 3 O 0 S O
CO 4> — O -C T -O II —
Q. 0 4> » C
OC>CrH(BlO •*-
— 43 1 O <*- 1 O
— « 43 .- o CM (A -O t.
O C O 0) 0) CM— C Q.
U — O O M O T OCS
4> jQ 0 — — - t. >»
CSC £ 43 rH 43 •- L
CO O43O(D«S'-'CE 4>
O C O) L. O Q. Ot
S O O O TJ COO. 3
rH C -C — 1. C 0 O -O
^4>— 09.C— CS C
I- Q. > 43 43 O CJ M CO
«l-Eax-^O— U> TH
OO ^•(A3h.^-sl-EII OT 0
CO OOCCOCO 0 ~^ —
O> •— t. O •* tH c ^ ^
4» •-0*-'COC — ffl
1O Q. C 43 — £ — O •- O H
o j: o Q. « 3 in IE- -o
I-3E4>— «AT>ata O E
— TJCJIAO— -OO.' Z O
O 0XOUE81O 1.
1. • L. O U C (9 43 <*-
43 co - »08» •- t. 0 3 CO ^ 0 «
CM U t •— • — v^ E  — IO •- C CM -O •- O U
o> w c CD <*- o c — t. a
0COt.O->0 — J3 — 3
t. E — n (o .c >%«— u o (A
3 « E o w 43 — OL. a co 4>
•aco)>o049
490co-oEaO^*— *r-*0Q. 3 tf-^491 TJ — ^ C- O
— T3 0) «t- lH U) rH 0||4> 49 —tH O
490c0 otocA a a-
o i- o i c o • arHo E 4> CM c
0 — 4>E * A *-> 0 J* • 0
«»• W 4> (A 3 — to — U OO
<*-co.o— aco e w o «i- a
C O O 0 O C ^-^ L— t 0C 49
i — o— « o 43 co i- o a
s-\0 43 0) — -O CO 0) t- C CD a •— Q
— ^ 0) 0) O C - U 43 IO 43 O ID 4>
ac o •- (. a T a w co .co
co o e 43 e o -c o tHo0
•-•- 0C>» OCDO0 — CO 49
CD 43 0 O^-t00 3 — 0 49 C
I. O -C «t- O O I. J: IB O .y-v— rH0 C TJ.^,
•DC 0c.(Aacaioa >0 o c c T>
00 « o » >-• h-E C40^— 00 a
c— 0 c -cooc — (-(/>•- S.
0 « I. C C 0) « « O O (A MO.X
>(A Q. — > « M rH —0 — W < 43
•— •— — 0 0 *-f — 49 > C ._ ._
43 E C T) 43 C C 9 O. — ,— . 0 E » 49
O0 — 0000C49 O > O C CL0«a
«H» a » f- • - .- ._ 0 — 490. c c a 3
«r-494949E OO •— O.O CT
0-x» — 00000 i-0ta —
co CA 0031. 49 — (a 0 a a JT
43 S — C C «t- 
-------
8.3.4  Facility Closures
     The costs of compliance will move each firm's average variable cost
(marginal cost) upward.  As a consequence of market adjustments of supply
and demand, the economic model predicted that the new equilibrium price of
hazardous waste services would be higher and the new market quantity lower.
The reduced quantity of hazardous waste services implies reduced capacity
utilizat4on rates across the industry, and possibly facility closures.
     The basic economic model of facility closures posits that if the price
of the commodity does not cover average variable cost, then total costs
exceed total revenue and the firm should close the facility.  Porter15
identifies a number of reasons why closures may not always accompany such
situations:
     •    Existence of durable and specialized assets
     •    Presence of closure costs
     •    Absence of precise information on revenues and costs
     •    Existence of other managerial or emotional factors
     •    Absence of a mechanism for  asset disposition.
     However,  the basic facility model is intuitively appealing  and is
capable  of identifying possible closure candidates.  For captive facili-.
ties, using the market price is especially problematic because the
hazardous waste management  services are the result of an internal transac-
tion and do not take place  in a market.  However, the market price is the
best surrogate available for the marginal benefit of the captive-provided
hazardous waste management  services.   Also, simple hazardous waste manage-
ment cost functions are used that represent the general relationship
between  hazardous waste management output and costs.  Undoubtedly, many
other important factors that affect production costs are ignored here.
Thus, the  results can  only  suggest the general magnitude of the  facility
closure  pressures that the  options may create.
     Table 8-23 shows  the possible facility closures given the assumptions
employed in this analysis:
     •     Hazardous waste management  services are competitively
           produced.
                                     8-41


-------
     •    Each hazardous waste management facility has constant costs
          to the capacity utilization rate,  and infinite costs there-
          after.
These assumptions lead to the conclusion that some very small facilities
would be uneconomical and would experience pressures to close under the
control options.  However, given the nominal reduction in hazardous waste
generation, it is doubtful that few, if any, of the closures predicted by
the model would actually take place.  There are several reasons for this
interpretation of the results:  (1) The reductions in hazardous waste
generation are likely to be distributed across all generators.  Thus, each
generator will slightly reduce the operating rate of the hazardous waste
management facility.  (2) The permitting process for a hazardous waste
management facility  is long and costly.  Facilities with transferrable
permits are likely to become more valuable when market prices for waste
management services  are rising.  Firms that run facilities with trans-
ferable permits* are likely to sell the permits to more efficient entre-
preneurs.  (3) Transportation costs will preclude some of the projected
real locations of waste management.   (4) Closure costs can be very substan-
tial.
8.3.5  Employment Effects
      Increases  in the cost of waste management services are projected to
slightly reduce the  quantity of these services.  The possible changes in
jobs  due to these reductions is presented in Table 8-24.16  These estimates
are for the hazardous waste industry and are the direct consequences of the
potential  plant closures  in Table 8-23.  The number of jobs  in the TSDF
industry are  estimated using a regression model.  A representative sample
of facilities was selected from the  SAM  Industry Profile data base and the
number of  production workers and amount of  hazardous waste obtained.17  A
simple linear regression  model was  used to  estimate the relationship
between number  of jobs and production quantity:
 transferable  permits  allow  a  business to  sell  the  permit  to  a  potential
  buyer  of  the  facility.
                                     8-43

-------







1
w



§
P
Q
_J
g
^™
gj»
o


^"
CD •
en S
\ff CD
*^ ^?

Ul
I rk

Ul ^^
_ oc
J™ LU
ZZ 29
«| 3

^™ Z>
O
3
2
CM
1
CO
111
S


1

1





c
o
•—
4>
o
_
2
c
o
u













LO




*




to



CM







•^4













.
•

L.
O
o
0
to



1 O> 1 It
t



1 O> 1 II



r-IQQLOOOISQCOQ
f-4 I CO O> 1 II
1 i-H 1
1


1-4 1 CO O) 1 II
1 1-1 1
1




?10 CO S 5» CO O
CO OJ 1 II
1 rH 1
I





«.
— a
o a o

c »~
CD C C
t. -c a
° °
OS -O — 3
C C • C
3 " .2 1
« c o -a L.
49 — — B 43
O L, C E 9
-i a S . *
o « L. — n •>
L. « 0 (I 49 •)
CL 49 C U U 49
O — — 3 O
— 3 49 -O 3
— TJ ~ 3 O -O
— O (ft 9 C O
E «- — U CL U
CL IB a CL
0 0 E —
— t..- « L. (B -O W
— 0EC.KO0U
49 CL 0 0 JC — — —
x IB JC J3 CL E — 49
.g a ° £ .J'SS
» — — O —
C t. — (A U -D C
«"5i^»5"J-
CC— (ft 49 O I. 49 0
'c *• L. TJ • o (ft — J3
zou.i-ia_m-k CL
0 ~3
C or
— 0
U C
a o
49 (ft
— • 49
.? 1 i
t. CL 3
49 (ft l_
O C ^^
O a o)
— t. c
Ul t- M


S S S




S ? 0



IS S IS
1



S S S






Q S O
1













(ft
0
facturing
ti 1 ities-
wholesale sa
3 3
C
IB (ft (ft
E IB -0
(ft O
3 -0 O9
O C
0 (1 0
IB o ja
^ •_ fg
— L. U
0 49 3
o o -o
(ft 0 C
3 UJ Z


s -»•




S V



s - c
— a
C JC
\ S
n in
— a
3 *
CL 3
(ft O
o -o
JC L.
« N
« (B
ja jc

co
1


O)
tH
co
1




0>
rH
co
1














Ul
»
49

«
T3 IB
0 E
(ft —
O 49
— (ft
U 0
0 (ft
JC —
49
(0
E 0
U 49
€,_ ._
^•N*—
U U
IB a
0 •*-

<- 0
0 in
a. o
0) U
0 9
""49
(^
0 C

L.
9 (ft
J3 J3
E 0
3 — >
C

O
(ft
9 t-
01 9
M J3
0 E
— 3
C.

O 9
.-,£
0
49 •
CO
O9CM
C 1
1 0
3 —
(ft J3 ••
-Q T3
C O
0 '
49 -D C
3 0 O
rU 'iff
0 (ft «
o— •> 0 cr
o u
Iff 1. 09 CO
— CL 0
0.,1" *
- 0 9 <
J3 — JC
— 09 _1
(ft — C
— o —
JC IB M
h- » CB (.
— 09 19
49 L.
C O (A
O C
CEO
.— CL —
E CL49
O CL
•0 IS 0
9
t. II —
CL O
iH L.
•D <-'49
0 C
(ft (ft O
(0 — O
J3 O
t- 0
0 49 —
L C CL
(B O E
u a
LO X
O9 0
3 (ft JC
0 — t-
JC >
49 _0 •
""* 0 ^
(ft > O.
o *•• o
494.1
CL 0 -
O 0 (O
t- L. LO
49
C -D -O
O C C
O.I.
8-44

-------
                                 L = A + BQ
where
     L'= number of production workers
     Q = quantity of waste (Mg/yr)
     A = intercept of the regression
     ,B = slope of the regression.
The estimated regression equation was statistically significant (5 percent
level of statistical significance).
     Table 8-24 indicates that the number of hazardous waste management
jobs is likely to decline overall.  The number of jobs lost in the regula-
tory options 1 to 5 is less than 1.5 percent of the total number of jobs
before the regulation.  The number of jobs for the hazardous waste industry
is presented in Appendix I, section I.A.
     The regulatory costs identified and estimated above are annualized
capital and operating costs of the options.  There may also be one-time
dislocation costs to workers due to the projected output changes.  No
attempt is made here to value the costs of these dislocations.  Insignifi-
cant reductions in other jobs at captive facilities are projected due to
the  projected reduction in output.  All generating sectors were projected
to reduce the number of jobs in their hazardous waste management facilities
in proportion to the reduction in their hazardous waste management
activity.
     Clearly, these projected reductions in jobs may not be translated one-
for-one into worker dislocations.  Firms may move workers between jobs,
taking advantage of other demand shifts or attrition though resignations
and  retirements.
8.3.6  Small Business Effects
     The Regulatory Flexibility Act requires Federal agencies  to analyze
the  effects of their regulations on small entities and to involve these
entities more actively  in developing and reviewing regulations.  "Small
entities" here includes small businesses, small governmental jurisdictions,
and  small organizations.  The purpose of the Regulatory  Flexibility  Act  is
to minimize the effects of the environmental regulations on small entities.
                                     8-45

-------
      The regulation  of TSDF affects  the hazardous  waste  generators who
 supply onsite waste  management  services (captive facilities),  and the
 suppliers of commercial  hazardous  waste management services  (commercial
 facilities).   The criteria for  "smallness"  applies to  the  firm,  not to the
 facility.  The Small  Business Administration  (SBA)  defines  "small busi-
 nesses"  by industry  (by SIC code)  in terms  of annual sales  or  employment.
 (The  SBA size criteria for each industry are  shown in  Table  8-25.)  Deter-
 mining the size of the business that owns a hazardous  waste  management
 captive  facility (a  facility generating and managing some  or all waste on
 site)  is complex because waste  management is  a secondary activity of the
 business.  These captive facilities  in  the  industrial  sectors  are owned by
 businesses that produce products such as petroleum products, solvents,
 chemicals,  etc.,  besides supplying hazardous  waste management  services.
 The determination of  the ownership of commercial facilities  is less complex
 because  the primary  activity of such businesses is  hazardous waste manage-
 ment  services.   Therefore,  the  formal analyses  of  small  business effects
 were  limited  to the commercial  facilities.  However, some  general conclu-
 sions  are drawn for captive facilities  at the end  of this  section.
     A several-step process was initiated to  investigate the potential
 small  business  effects  for commercial facilities.   Information on the U.S.
 Environmental  Protection Agency (EPA) facility  identification number, the
 SIC code,  and  the volume entering  hazardous waste management processes was
 gathered  from  the Industry Profile Data  Base.  Using the baseline hazardous
waste  management  service price  of  $l,280/Mg and volume from the data base,
 annual sales of waste management services were estimated (volume of hazard-
 ous waste management service multiplied  by  the baseline  price) for each of
 the 136  commercial facilities.  The  SIC  codes used  to  identify commercial
 facilities  include SIC 4212 (local trucking and storage), SIC 4213 (truck-
 ing, without storage), SIC  4953  (refuse  systems), and SIC 7399 (business
 services, not elsewhere classified).  A  uniform annual  sales cutoff equal
to $3.5 million is used to  identify  potential small businesses among the
commercial facilities instead of the  SBA  annual sales cutoff (SIC 4953)
equal to $6 million.   The choice of  $3.5 million is likely to overstate the
small business effects from the regulation.   Thus,  the number of small
businesses identified, 16,   is likely to overstate the actual value.
                                    8-46

-------
           TABLE 8-25.   SMALL BUSINESS ADMINISTRATION SIZE
                         CRITERIA BY SIC CODEa
     SIC Code
SBA Cutoff
     2800
     2869
     2899
     3811
     4953
     4959
     5161
     5172
     7399
     8999
Does not exist
1,000 employees
500 employees
500 employees
$6 million
$3.5 million
500 employees
500 employees
$3.5 million
$3.5 million
aThe Small Business Administration (SBA) uses annual sales and
 employment figures to determine the size of business entities, by
 Standard Industrial Classification (SIC) code.  The SBA cutoff
 figures for "Small business" classification listed in this table
 were used to determine which of the 136 commercial hazardous waste
 management facilities could be designated as "small" (between 11
 and 15).  The next step was to assess the economic impact of the
 regulation on these small firms.
                                  8-47

-------
      Of the 136 commercial  facilities,  101  are  estimated  to  have  annual
 sales greater than  or equal  to $3.5  million and hence  are not  considered
 small businesses.   The remaining  35  facilities  have  estimated  annual  sales
 of less than $3.5 million  and  are potential candidates for small  business
 classification.
      The survey forms for  these 35 facilities from the National Survey of
 Hazardous Waste Treatment,  Storage,  Disposal, and Recycling  Facilities18
 were  examined to acquire more  detailed  information about  the facilities and
 the firms that own  them.   From these forms,  the following items of  informa-
 tion  were gathered:
      •     Facility  name, contact  person,  and telephone number
      •     Name of the business owning the facility
      •     Names of  other facilities  also  under  the same ownership
      •     Types of  hazardous waste management services performed
      •     Prices charged for hazardous waste management services
      •     Number of persons employed
      •     Current status of the facility  (active or  out of business).
      Of  the  35  facilities examined,  7 are owned by businesses with  sales
 greater  than  $3.5 million and  hence were  determined  to be large.  Ten of
 these 35  facilities were verified  to be small because  they were owned by
 businesses with sales  less than $3.5 million.   Twelve  of  these facilities
 have  gone  out of business and  are  no longer active.  The  survey forms for
 the remaining five facilities were not readily  available, but they  are
 likely to  be  small.  On the basis of this determination,  between 10 and 16
 facilities of the 136 total commercial facilities are  likely to be  poten-
 tial  small businesses.
      Table 8-26 presents the baseline statistical data  on the 16 potential
 small  businesses.  These facilities supplied hazardous waste management
 service  (annual waste quantity) between 2 Mg and 2,300 Mg.  Their annual
management costs were between $400 and $1.7 million.    The annual revenue
 from  hazardous waste management services  from these facilities was  between
$2,000 and $3 million.
                                    8-48

-------
       TABLE 8-26.   BASELINE  STATISTICAL  DATA  FOR  SMALL  COMMERCIAL
           FACILITIES  WITH ESTIMATED  SALES  REVENUE  LESS THAN
                     $3.5 MILLION  (ANNUAL VALUES)3
  Facility13
   Waste
quantity, Mg
  Service      Service
cost,c $103  sales,d $103
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
2
2
7
19
62
70
94
175
438
744
951
981
1,111
1,965
2,201
2,346
0
2
1
24
62
59
104
22
78
265
226
420
62
1,686
91
94
2
2
9
24
79
90
119
223
559
949
1,213
1,252
1,417
2,507
2,808
2,993
aThis table presents the baseline statistical data on the key vari-
 ables such as hazardous waste management services supplied (Mg/yr),
 annual hazardous waste management costs ($/yr),  annual revenue from
 hazardous waste management services ($/yr),  and profits (dollar
 differences between annual revenue and annual costs) for the
 potential small businesses.

^Facility codes are not used so as to protect the anonymity of each
 facility.

cService costs were estimated using cost functions.

dService sales = Waste quantity times baseline price of $1,275.84.
                                    8-49

-------
      The next issue is  whether the  regulation  would  have  "a  significant
 economic impact on  a substantial  number  of  small  entities" was  examined.  A
 "substantial  number" is generally thought to imply greater than 20  percent
 of the small  entities,  although this  is  not a  fixed  rule.  A "significant
 economic impact"  is said to  occur whenever  any of the  following criteria
 are satisfied:
      •    Annual  compliance  costs (including annualized capital,  oper-
           ating,  and reporting costs)  increase as a  percent  of  total
           costs of  production  for small  entities  for the  relevant
           process or product by more  than 5 percent.
      •    Compliance costs as  a percent  of  sales  for small entities
           are at  least  10 percent higher than  compliance  costs  as a
           percent of sales for large  entities.
      •    Capital costs  of compliance represent a significant portion
           of  capital  available to small  entities, considering internal
           cash  flow plus external financing capabilities.
      •    The requirements of  the regulation are  likely to result in
           closures  of small  entities.
      To  assess  whether  the economic impacts on small businesses  are likely
to  be significant,  the  four  criteria  are examined.   Table 8-27  summarizes
the with-regulation  implications  of control option 1, the most  stringent of
the options.  The first column  presents  the facility number.  Column 2
provides the  ratio  of compliance  costs to production cost.   The  ratio of
compliance costs  to  annual sales  for  the small  businesses is presented in
column 3.  Column 4  presents the  ratio of capital costs to annual sales for
each  small businesses.  Finally,  column  5 identifies the small  businesses
that  are potential closure candidates.
      The compliance  cost increases as a percent of total costs of
production for  small  businesses are less than 3.5 percent for all small
businesses.
     The compliance  costs as a percent of sales for small  businesses are
less than 2 percent.  The estimated ratio of compliance costs to  total
sales for the 16 small businesses is 0.28 percent.  For the  larger busi-
nesses, the estimated ratio of total compliance costs to total sales is
0.26 percent.  The compliance costs  as a percent of sales  for small
                                    8-50

-------
    TABLE 8-27.   EFFECTS  OF  THE MOST  STRINGENT  REGULATION  (OPTION  1)  ON
              SMALL  COMMERCIAL  FACILITIES  WITH ESTIMATED  SALES
                       REVENUE  LESS  THAN $3.5 MILLION3
Facility^
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
Compliance
cost/cost0
308
986
307
402
824
98
70
203
337
2,669
3,607
1,200
878
942
735
771
Compliance
cost/sales11
38
652
38
401
647
65
61
20
47
743
602
401
38
631
24
24
Capital
cost/sales6
62
1,222
62
939
1,213
113
168
33
63
1,548
1,303
939
62
1,427
29
28
Potential
closure
candidate
N
N
N
Y
N
N
N
N
N
N
N
N
N
N
N
N
N = Not likely to close.
Y = Potential for closure.

aThe postregulatory financial implications of regulatory control option 1
 are summarized in this table.  Column 2 represents the ratio of annual
 compliance costs (annualized capital and operating costs) and annual
 hazardous waste management costs.  Column 3 represents the ratio of
 compliance capital costs and annual profits.  Column 4 represents the
 ratio of compliance costs and annual revenue, and column 5 represents the
 ratio of compliance capital costs and annual revenue.  Data for this
 table are obtained from the Source Assessment Model  (SAM) Industry
 Profile data base, Appendix D, Section D.2.1.

^Facility codes are not used so as to protect the anonymity of each
 facility.

cCompliance costs ($) per $100,000 of waste management costs.

dCompliance costs ($) per $100,000 of revenue received.

eCapital costs  ($) per  $100,000 of revenue received.
                                     8-51

-------
 businesses are less than 10 percent higher than the compliance costs  as  a
 percent of sales for large businesses.
      The capital costs as a percent of  sales for small  businesses  are less
 than 2 percent.   Because the compliance capital costs represent a  small
 portion of the total  amount of sales,  it is reasonable  to conclude that  the
 capital costs of compliance represent  an insignificant  portion of  the capi-
 tal  available to small businesses.
      The economic impact model  estimates that 6 of the  larger businesses
 and  1 of the 16  small  businesses  are potential  closure  candidates  if  all
 the  projected quantity adjustments  are  registered on the  highest-cost
 facilities.   However,  given the nominal  reduction in hazardous waste
 generation,  it is likely that  these adjustments will be spread over many
 facilities.   Thus,  it  is doubtful that  any of the closures  predicted  by  the
 model  would  actually take place.
      The analysis indicates that  the economic impacts on  small  businesses
 are  not "significant"  using the criteria outlined above.  The TSDF process
 is a component of the  cost of  production for captive facilities.   As  shown
 in Table 8-6,  at the industry  level, TSDF costs are estimated to represent
 a very small  share of  production  costs.   Thus,  even large hazardous waste
 treatment  costs  would  not typically be  significant  as a percent of the
 costs  of the  entire plant.   Table 8-27  shows  that the highest share of
 compliance to production  costs  for  any  small  commercial businesses  is  less
 than 5  percent.   Given these values, it  seems  reasonable to conclude  also
 that it  is unlikely that  there  would be  any  significant impact  on  small
 businesses in  the  captive sector.
 8.4  REFERENCES
 1.   Booz-Allen  and Hamilton, Inc.  Review of Activities of Major  Firms  in
     the Commercial Hazardous Waste Management  Industry:  1982  Update.
     Exhibit  5.   Prepared  for U.S.  Environmental  Protection Agency, Office
     of  Policy Analysis.   Washington, DC.  August 15, 1983.
 2.   Development  Planning  and Research Associates,  Inc.  RIA  Mail  Survey
     Questionnaire.  Prepared for U.S.  Environmental  Protection Agency,
     Office of Solid Waste.  Washington, DC.  1981.
3.   Industrial Economics,  Inc.  Regulatory Analysis  of Proposed Restric-
     tions on Land Disposal of Hazardous Wastes.  Prepared for U.S. Envi-
     ronmental Protection Agency,  Office of Solid Waste.  Washington,  DC.
     May 1985.  Exhibit 4.
                                    8-52

-------
4.
5.
6.
7.
8.
9.
Temple, Barker, and Sloane,  Inc.  New England Regional Hazardous Waste
Pilot Project:  Phase I Briefing.  Prepared for U.S. Environmental
Protection Agency, Region I, Boston,  MA.  May 1985.  p. IV-18.

National Council of the Paper Industry for Air and Stream Improvement,
Inc.  The Land Application and Related Utilization of Pulp and Paper
Mill Sludges.  Technical Bulletin No. 439.  New York, NY.  August
1984.  p. 117-122.            . v  .

ICF, Incorporated.  The RCRA Risk-Cost Analysis Model, Phase III.
Appendixes B and D.  Prepared for U.S. Environmental Protection
Agency, Office of Solid Waste. Washington, DC.  March 1984.

Research Triangle Institute.  A Profile of the Market for Hazardous
Waste Management Services.  Prepared for U.S. Environmental Protection
Agency, Office of Air Quality Planning and Standards.  May 1986.

Houthakker, H. S., and L. D. Taylor.  Consumer Demand in the United
States:  Analysis and Projections.  Cambridge, MA, Harvard University
Press.  Second Edition.  1970.  p. 87, 100, 115-120, 166-167.
Koutsoyiannis, A.  Goals of Oligopolistic Firms:  An
of Competing Hypotheses.  Southern Economics Journal
1984.
 Empirical  Testing
.   51(2):540-567.
10.  Reference 8.

11.  Reference 9.

12.  Muth, R. F.  The Derived Demand Curve for a  Productive  Factor  and the
     Industry Supply Curve.  Oxford Economic Papers.  16(2):221-234, July
     1964.

13.  Miedema, A. K.  The Retail-Farm Price Ratio, the Farmer's  Share, and
     Technical Change.  American Journal of Agricultural  Economics.
     58(4):750-756, November 1976.

14.  Gardner, B. L.  Determinants of Supply Elasticity  in Interdependent
     Markets.  American Journal of Agricultural  Economics.   61(3):463-745,
     August  1979.

15.  Porter, M.  E.  Competitive Strategy:  Techniques for Analyzing Indus-
     tries and Competitors.  New York  City, The  Free  Press.   1980.
     p.  303-320.

16.  Memorandum  from Chandran, Ram, RTI, to Docket.   September  19,  1988.
     Estimation  of  Number  of Workers in  Treatment,  Storage,  and Disposal
     Facilities  (TSDF).

17.  Reference 16.
                                     8-53

-------
18.  Research Triangle Institute.  Small Business Analysis.  National
     Survey of Hazardous Waste Treatment, Storage, Disposal, and Recycling
     Facilities.  Prepared for U.S. Environmental Protection Agency, Office
     of Solid Waste.  Research Triangle Park, NC.  1987.
                                   8-54

-------
          APPENDIX A



EVOLUTION OF PROPOSED STANDARDS

-------

-------
                                APPENDIX A
                      EVOLUTION OF PROPOSED STANDARDS


     The EPA Office of Solid Waste and Emergency Response (OSWER)  first
initiated the development of air emission standards for hazardous  waste
treatment, storage, and disposal facilities (TSDF) in 1978.   In December
1978, OSWER proposed air emission standards for treatment and disposal of
hazardous waste based on an approach that included definition of volatile
waste solely in terms of its vapor pressure and use of the U.S. Occupa-
tional Safety and Health Administration (OSHA) levels for determining
acceptable emission levels (43 FR 59008, December 18, 1978).  A supple-
mental notice of proposed rulemaking was published on October 8, 1980
(45 FR 66816).
     The 1978 and 1980 actions were reproposed in 1981 (46 FR 11126,
February 5, 1981); the proposed standards included requirements for systems
to monitor ambient air quality and gaseous emissions, sampling and analysis
plans, data evaluation by predictive models, and recordkeeping/reporting.
General control requirements to prevent wind dispersion of particulate
matter from land disposal sources also were proposed.  The final standards
adopted by EPA included the particulate control requirements, but they did
not incorporate any other measures for air emission management
(47 FR 32274, July 26, 1982).
     In February 1984, EPA considered the need to further evaluate air
emission standards and delegated authority to the Office of Air Quality
Planning and Standards (OAQPS) to develop standards for air emissions from
area sources at TSDF.  At that time, OAQPS initiated the project that led
to this draft background information document  (BID).  The program plan
outlining the technical and regulatory approaches selected for the project
was reviewed by the National Air Pollution Control Technique Advisory
Committee  (NAPCTAC) meeting held August 29-30, 1984.  The NAPCTAC is
composed of 16 persons from industry, State, and  local air pollution
agencies, environmental groups, and others with expertise in air pollution
control.   In November 1984, Congress passed the Hazardous and Solid Waste
Amendments (HSWA) to the Resource Conservation and Recovery Act (RCRA) of
                                    A-3

-------
  1976.   Section  3004(n) of  HSWA  specifically directs the Administrator to
  establish  standards  for the monitoring  and control of air emissions from
  hazardous  waste TSDF as necessary to protect human health and the
  environment.  It  is  under  the authority of Section 3004(n) that these
  standards  are being  developed.
      This  OAQPS study to develop air standards for TSDF air emissions began
 with the collection  of information on waste management processes, hazardous
 waste characteristics, and controls that could potentially be applied to
 reduce air emissions.  This information was obtained through site visits
 and sampling surveys, industry surveys, various Agency data bases, and
 testing programs.   Additional  information was gathered through literature
 searches, meetings, and telephone contacts with experts within EPA,  State
 and local regulatory authorities, and affected industries.  Based on this
 information,  preliminary draft BID chapters,  which described the TSDF
 industry, emission sources, and potential  controls were prepared and trans-
 mitted to representatives  of industry,  trade  associations, and environ-
 mental  groups for  review and comment in February 1986.   The comments
 received were analyzed  and  incorporated in the BID,  as  were additional data
 obtained through test programs,  other data bases,  and  internal  EPA review.
        V
      Public comments  were also solicited on three  specific aspects of the
 project.   In  February 1987, comments  were  solicited  from TSDF  operators,
 major trade associations, and  environmental groups on potential  test
 methods  for determining the volatile  organic content of  hazardous  wastes.
 In March  1987, a draft report  on  predictive models for estimating  organic
 air emissions was  mailed out for  public  review.  This report was  finalized
 and distributed  in December 1987.   (See  "Hazardous Waste Treatment,
 Storage,  and Disposal Facilities  [TSDF]  -  Air  Emission Models,"  EPA-450/3-
 87-026.)  On June  9,  1987,  OAQPS  presented  a status report on the  project
 and test method  development work  at a public meeting of the NAPCTAC.
     Under  a separate project,  the OAQPS proposed  its initial set  of TSDF
 air standards for  organic emissions from process vents and equipment leaks
 (52 FR 3748, February 5, 1987).  At that time, EPA requested comments from
TSDF operators, trade associations, and environmental groups on the
proposed air controls.  A public hearing was held  on March 23, 1987, in
                                    A-4

-------
Durham, North Carolina, to obtain external  comments on the proposed
standards.  These standards were promulgated on June 21,  1990
(55 FR 25454).  Additional Information on this project can be found 1n
Docket Number F-90-AESP-FFFFF.
    On April 5, 1988, OAQPS distributed the draft BID for review to
NAPCTAC members, Industry representatives,  and environmental  groups prior
to the NAPCTAC meeting held May 18, 1988.  Also distributed for review were
draft papers titled, "Preliminary Control Strategies for TSDF A1r Emission
Standards," and "Method for the Determination of Volatile Organic Content
of Hazardous Waste."  This .meeting, open to the public, provided an
additional opportunity for industry and environmental groups to comment on
the draft rulemaking prior to proposal.  This BID reflects revisions that
have been made based on comments received since NAPCTAC review.  Major
events that have occurred in the development of background information for
the proposed standards are present 1n Table A-l.
                                     A-5

-------
           TABLE A-l.  EVOLUTION OF PROPOSED TREATMENT, STORAGE,
                     AND DISPOSAL FACILITY AIR STANDARDS
      Date
                       Event
 November 1983
 December 1983
 February 1984


 August  29-30,  1984



 November 9,  1984


 November 9,  1984
April 24,  1985


January 8, 1985



October 1985




February 6, 1986


March 6-7, 1986
 Contractors begin site visits and source sampling  at
 over 100 TSDF;  testing under OAQPS/ORD/OSW program
 extending through 1986 also begins.

 Meeting with Chemical  Manufacturers  Association  to
 review "Evaluation and Selection of  Models for
 Estimating Air"Emissions from Hazardous  Waste
 Treatment, Storage,  and Disposal Facilities,"
 "Assessment of  Air Emissions from Hazadous Waste
 Treatment, Storage,  and Disposal Facilities:
 Hazardous Waste Rankings,"  and "Assessment of Air
 Emissions from  Hazardous Waste Treatment,  Storage,
 and  Disposal  Facilities:  Preliminary  National
 Emissions Estimates."

 OSWER delegates  authority for development  of  air
 standards for TSDF area sources to OAQPS.

 National  Air Pollution Control  Techniques  Advisory
 Committee meeting held in Durham,  North  Carolina,  to
 review TSDF program  plan (49 FR 26808).

 Congress  passes  Hazardous and Solid  Waste  Amendments
 to Resource Conservation and Recovery  Act  of  1976.

 Meeting with  Chemical  Manufacturers  Association
 Secondary Emissions  Work Group  to  review and  comment
 on draft  technical note,  "Basis for  Design of Test
 Facility  for  Flux Chamber Emissions  Measurement
 Validation."

 Meeting with  American  Petroleum Institute  to  discuss
 status of standards  development for  land treatment.

 Meeting with  Chemicals  Manufacturers Association to
 discuss current  studies  of  air  source  emissions  from
 TSDF.

 Research  Triangle Institute  begins work  to develop air
 emissions  for hazardous  waste treatment, storage, and
 disposal  facilities, under  EPA  Contract  No. 68-02-
 4326.

Mailout of preliminary  BID Chapters 3.0 to  6.0 to
 industry  and environmental groups.

Meeting with Chevron Chemical Co. to discuss  planned
 landfarm  simulation study.
                                    A-6
                                                                  (continued)

-------
                          TABLE A-l  (continued)
     Date
                      Event
April 24, 1986


May 14, 1986


December 17, 1986


February 5, 1987


February 11, 1987


March 23, 1987



April 10, 1987


June 9, 1987



September 30, 1987


December 10, 1987


January 14, 1988


April 5, 1988
Meeting with American Petroleum Institute on status
of TSDF standards development.

Meeting with Chemical Manufacturers Association to
discuss project status and BID comments.

Meeting with American Petroleum Institute on land
treatment air emission research.

Proposal of accelerated standards for selected
sources at hazardous waste TSDF (52 FR 3748).

Mai lout of draft test method approach document to
industry and environmental groups.

Public hearing for accelerated rulemaking for
selected sources at hazardous waste TSDF held in
Durham, North Carolina.

Mailout of draft report on organic air emission models
to industry and environmental groups.

Meeting of National Air Pollution Control Techniques
Advisory Committee to review project status and test
method development program (52 FR 15762).

Meeting with Chevron Chemical Corporation to discuss
land treatment data.

Mailout of final report on organic air emission
models to industry and environmental groups.

Meeting with Chemical Manufacturers Association to
discuss project status.

Mailout of preliminary draft BID to National
Air Pollution Control Techniques Advisory Committee,
TSDF operators, trade associations, environmental
groups, and other public groups.

                                            (continued)
                                    A-7

-------
                            TABLE A-l   (continued)
     Date
                                            Event
                      Meeting of National Air Pollution Control Techniques
                      Advisory Committee to review preliminary draft BID.

                      Meeting with Chemical Manufacturers Association to
                      receive comments on preliminary draft BID.

                      Meeting with Chemical Manufacturers Association to
                      receive comments on volatile organics test method.

                      Promulgation of accelerated standards for TSDF
                      process vents and equipment leaks (55 FR 25454).

TSDF
OAQPS
ORD
OSW
BID
May 18, 1988


July 27, 1988


August 16, 1988


June 21, 1990
        Treatment, storage, and disposal facility.
        Office of Air Quality Planning and Standards.
        Office of Research and Development.
        Office of Solid Waste.
        Background Information Document.
aThis table presents those major events that have occurred to date in the
 development of background information for the TSDF air standard.
                                     A-8

-------
                 APPENDIX B



INDEX TO ENVIRONMENTAL IMPACT CONSIDERATIONS

-------

-------
                                APPENDIX B
               INDEX TO ENVIRONMENTAL IMPACT CONSIDERATIONS
     This appendix consists of a reference system that is cross-indexed
with the October 21, 1974, Federal Register (39 FR 37419) containing EPA
guidelines for the preparation of Environmental Impact Statements.  This
index can be used to identify sections of the document that contain data
and information germane to any portion of the Federal Register guidelines.
                                     B-3

-------
                                  APPENDIX B
                 INDEX TO ENVIRONMENTAL  IMPACT  CONSIDERATIONS
 Agency guidelines  for preparing
 regulatory action  environmental
 impact statements  (39 FR  37419)
 Location within the Background
 Information Document (BID)
 1.  Background and  description

    a.   Summary of  control
        options


    b.   Industry affected by the
        control  options
   c.  Relationship to other
       regulatory Agency actions


   d.  Specific processes affected
       by the control options
 A description of the control options
 is provided in Chapter 5.0 of BID
 Vol. I.

 A discussion of the industry affected
 by the control options is presented in
 Chapter 3.0 of BID Vol.  I.

 The relationship to other regulatory
 Agency actions is discussed in Chapter
 5.0 of BID Vol.  I.

 The specific processes affected by the
 control  options  are summarized in
 Chapter 3.0 of BID Vol.  I.
2. Impacts of the alternatives

   a.  Air pollution
   b.   Water pollution
   c.   Solid waste  disposal
  d.   Energy  impact
 The  air  pollution  impacts  are  dis-
 cussed in  Chapter  6.0  of BID Vol.  I.
 Supplementary  information  on the
 emission models  and emission estimates
 is included  in Appendix C  of BID
 Vol.  I.  Appendix  D of BID Vol. II
 describes  the Source Assessment Model
 used  to estimate nationwide emissions
 and their  correlations to  test
 methods.   Test data are presented in
 Appendix F of BID  Vol. II.

 The water  pollution impacts are
 described  in Chapter 6.0 of BID
 Vol.  I.

 The solid waste disposal impacts are
 discussed  in Chapter 6.0 of BID
 Vol.   I.

The energy impacts are discussed in
Chapter 6.0 of BID Vol. I.
                                                                   (continued)
                                   B-4

-------
          INDEX TO ENVIRONMENTAL IMPACT CONSIDERATIONS (continued)
Agency guidelines for preparing
regulatory action environmental
impact statements (39 FR 37419)
Location within the Background
Information Document (BID)
   e.  Cross-media impacts
   f.  Economic impact
   g. Health impact
Cross-media and secondary air environ-
mental impacts are discussed in
Chapter 6.0 of the BID Vol. I.  Addi-
tional information is presented in
Appendix K of BID Vol. III.

The cost and economic impacts of
control options are presented in
Chapters 7.0 and 8.0 of BID.Vol., I.
Supplementary information on control
costs and on the economic impact
analysis is included in Appendixes H
and I of BID Vol. III.

Incidence and risk impacts are
presented in Chapter 6.0 of BID
Vol.  I.  The health risk analyses are
discussed further in Appendixes D and
E of  BID Vol. II and Appendix J of BID
Vol.  III.
                                    B-5

-------

-------
              APPENDIX C



EMISSION MODELS AND EMISSION ESTIMATES

-------

-------
                                APPENDIX C
                  EMISSION MODELS AND EMISSION ESTIMATES

     The objective of Appendix C is to provide a link between
     •    Emission models used to estimate organic air emissions from
          treatment,  storage,  and disposal facility (TSDF)  waste
          management  units
     •    Model TSDF  waste management unit analyses used to develop
          estimates of emission reductions and costs of applying emis-
          sion control technologies
     •    The Source  Assessment Model (SAM),  which uses both the
          aforementioned to generate an estimate of nationwide TSDF
          organic air emissions and control costs.
     This appendix provides a discussion of the mathematical models used to
estimate nationwide air emissions from hazardous waste TSDF,  These models
represent most of the TSDF emission sources introduced in Chapter 3.0,
Section 3.1.  Some emission sources, such as drum crushing, are undergoing
analysis at this time.  The discussion of the emission models in Sec-
tion C.I includes a description of the models, a comparison of emission
model estimates with  results from specific field tests of TSDF waste man-
agement units, and a sensitivity analysis.
     To estimate emissions with these emission models, inputs such as waste
management unit surface area, waste retention time, and depth of unit are
essential.  Physical  and chemical characteristics.of the waste in the
unit—such as the specific organic compounds present and their concentra-
tions and knowledge of the presence or absence of multiple phases (e.g.,
separate aqueous and organic layers)--are also needed.
     Use of these emission models to develop estimates of nationwide emis-
sions requires some knowledge of the waste management unit characteristics
that could affect emissions for each TSDF in the country.  Given that only
                                    C-3

-------
 general information such as annual waste throughput is available for the
 thousands of TSDF, a model waste management unit approach was developed to
 facilitate emission estimates, as well as control emission reductions and
 control costs.  Descriptions of the model units and the basis for develop-
 ing the range of model units characteristics are given in Section C.2.1.
      As explained above, knowledge of waste physical and chemical charac-
 teristics is essential to emission estimates.  Emission reductions and
 control costs likewise are sensitive to waste properties, so a model unit
 analysis to derive emission reduction and control costs also requires a
 definition of wastes being managed in the model waste management units.
 Model wastes were defined for this purpose.   Section C.2.2 provides a dis-
 cussion of the selection of model  wastes and defines those wastes.
      Lastly,  in Section C.2.3,  control  costs and control  emission reduc-
 tions for a selected set of model  waste management units  are given in tabu-
 lar form.   The data contained  in  the table demonstrate the variations in
 costs and  emission reductions  that occur along with  variations in model
 waste compositions and degree  of  emission control  provided by different
 control  technologies.   These model  waste management  unit  control  costs  and
 control  emission  reductions  are the bases for extrapolating costs and emis-
 sion  reductions to nationwide  estimates.   Appendix D contains a  discussion
 of  the  procedure  for relating  costs  to  waste throughput in each  model waste
 management unit and then  extrapolating  for nationwide  cost estimates  via
 the SAM.  The emission  reductions  expressed  as  a  percentage of uncontrolled
 emissions are discussed  in Chapter  4.0  and Appendix  D.
 C.I   EMISSION MODELS
 C.I.I  Description of Models
     The emission models that are used  to estimate air emissions  from TSDF
 processes are drawn from several different sources.  These models  are
 presented in a TSDF air emission models report that provides  the  basis and
 description of each model, along with sample calculations  and  comparisons
 of modeled emissions to measured emissions using field test data.
     The emission models discussed in Chapter 3.0 are those presented in
the March 1987 draft of the TSDF air emission models report.1  Certain TSDF
                                    C-4

-------
emission models have been revised since that time,  and a final  version of
the report has been released (December 1987).2  The principal  changes to
the models involved refining the biodegradation component of the models to
more accuractely reflect biologically active systems handling low organic
concentration waste streams.  With regard to emission model outputs, the
changes, by and large, did not result in appreciable differences in the
emission estimates.   (Refer to Appendix D, Section D.2.4, for a more
detailed discussion.)
     In the emission models report, models are presented for the following
TSDF management processes:  surface impoundments and uncovered storage and
treatment tanks; land treatment; landfills and wastepiles; and transfer,
storage, and handling operations.  In general, the report describes the
chemical and physical pathways for organics released from hazardous wastes
to the atmosphere, and it discusses their relevance to the different types
of TSDF management processes and the sets of conditions that are important
in emission estimation.
     In the following paragraphs, the models are presented in simplified
forms or in qualitative terms.  For a full discussion, refer to the TSDF
air emission models report.
     C.I.1.1  Surface Impoundments and Uncovered Tanks.
     This section presents emission models for quiescent and
aerated/agitated surface  impoundments and uncovered tanks.  Quiescent
surface impoundments  where wastes flow through to  other processes  (i.e.,
storage and treatment) are addressed initially with uncovered tanks
(C.I.1.1.1).  Quiescent  impoundments without waste flowthrough, such  as
disposal impoundments, are discussed in the  next section  (C.I.1.1.2).
Aerated treatment  impoundments and uncovered tanks are discussed in
Section C.I.1.1.3.
     C.I. 1.1.1  Quiescent surface with flow.   Emission characteristics  from
quiescent uncovered  storage and treatment processes are  similar; therefore,
the same basic  model  was  used to estimate emissions from  all such
processes.  These waste management processes  for flowthrough emission
modeling include uncovered tank storage,  storage surface  impoundments,
uncovered quiescent  treatment tanks, and  quiescent treatment impoundments.
The modeling  approach used to estimate emissions from these types  of TSDF
management units  is  based on the work of  Springer  et  al.3  and Mackay and

                                     C-5

-------
 Yeun4 for the liquid-phase mass transfer and MacKay and Matasugu5 for the
 gas-phase mass transfer.  The emission equation used is a form of the basic
 relationship describing the mass transfer of a volatile constituent from
 the opened liquid surface to the air.  The model for flowthrough impound-
 ments and tanks assumes that the system is well-mixed and that the bulk
 concentration is equal to the effluent concentration.  A material balance
 for this yields:
                               QCQ = KACL + QCL
 where
        Q  =  volumetric flow rate,  m3/s
       C0  -  influent concentration of organics in the waste,  g/m3
        K  =  overall  mass transfer  coefficient, m/s
        A  =  liquid surface area, m2
       CL  =  bulk  (effluent)  concentration of organics,  g/m3.
 The  overall  mass transfer coefficient  is  based on:
                                  (C-l)
                          1
1
1
                                               KGKeq
                                                                       (C-2)
where
      K  =  overall mass transfer coefficient, m/s
     KL  =  liquid-phase mass transfer coefficient, m/s
     Kg  =  gas-phase mass transfer coefficient, m/s
     Keq »  equilibrium constant or partition coefficient, unitless.
     The air emissions from the liquid surface are calculated using the
basic relationship describing mass transfer of a volatile constituent from
the open liquid surface to the air:

                                 E = KACL                             (C-3)
                                    C-6

-------
where
      E = air emissions from the liquid surface,  g/s
      K = overall mass transfer coefficient, m/s
      A = liquid surface area, m^
     CL = concentration of the constituent in the liquid phase, g/m3.
     C.I.1.1.2  Quiescent surface with no outlet flow.  A disposal
impoundment is defined as a unit that receives waste for ultimate disposal
rather than for storage or treatment.  This type of impoundment differs
from the storage and treatment impoundments in that there is no liquid flow
out of the impoundment.  The calculation of the overall mass transfer coef-
ficient is the same as that presented for quiescent surfaces with flow.
However, the assumption that the bulk concentration is equal to the efflu-
ent concentration is not applicable here.  The emission-estimating proced-
ure differs in the calculation of the liquid-phase concentration that is
the driving force for mass transfer to the air.  The emission  rate can be
calculated as follows:
E =
                                    [1_exp  (.KAt/V)]
(C-4)
where
      E  =  Emission  rate, g/s
      V  =  Volume  of the  impoundment, m3
      t  =  Time  after disposal,  s
 and with  the other symbols as  previously  defined.   Reference 2 gives  a
 detailed  derivation of  the above  equation.
      C.I.1.1.3  Aerated systems.   Aeration  or  agitation  in  an aqueous system
 transfers  air  (oxygen)  to the  liquid  to  improve mixing or to increase biode-
 gradation.  Aerated hazardous  waste management processes include  uncovered,
 aerated treatment  tanks and  aerated treatment  impoundments.  A turbulent
 liquid  surface in  uncovered  tanks and impoundments  enhances mass  transfer to
 the  air.   Thus,  there are two  significant differences between the quiescent
 emission  model and the  aerated emission  model:  (1) the  modified  mass transfer
                                     C-7

-------
  coefficient  and  (2)  the  incorporation  of  a  biodegradation term.  The calcula-
  tion of  the  overall  mass  transfer coefficient  for mechanically aerated systems
  is based on  the  correlations  of Thibodeaux  and Reinhart for the liquid and gas
  phases,  respectively.6  The rate of biodegradation was assumed to be first
  order with respect to concentration based on experimental data in the form of
  a decay  model; this  is similar to the  Monod model at low loadings.
      A material  balance around the well-mixed system yields:
                  QCQ = QCL
                                             KCLA
(C-5)
 where
 Q
C0
 V
 K
 A
              volumetric flow rate, m3/s
              influent concentration of organics in the waste, g/m3
              bulk (effluent) concentration of organics in the waste,  g/m3
              pseudo first-order rate constant for biodegradation,  1/s
              system volume,  m3
              overall  mass transfer coefficient,  m/s
              surface  area, m2.
      Air emissions  can be estimated using Equation (C-3) .
      Additional  research  data  have been obtained on biodegradation rates  of
 specific constituents,  and numerous comments  were received  on the  emission
 and biodegradation  models. 6-5   Based on the new  information,  an  improved
 biodegradation model  was  developed that incorporates Monod  kinetics.   This
 model fits the available  biodegradation rate  data better than the  model
 described above  and generally provides  a sounder technical  basis for  evalu-
 ating the extent  of biodegradation.   The comments  also provided additional
 information on the concentration of organics  in  biologically  active treat-
ment processes and the  aeration parameters used  for the model  units.
 Proposed revisions to the aerated  units  and the  biodgradation  model were
evaluated in a sensitivity analysis  to  determine the effect on the nation-
wide impacts presented  in this document. 7  The results of the  analysis
                                    C-8

-------
showed that the combined effects of the proposed changes had only a minor
effect (less than 5 percent) on nationwide impacts.
     C.I.1.2  Land Treatment.  Emissions from land treatment operations may
occur in three distinct ways:  from application of waste to the soil sur-
face, from the waste on the soil surface before tilling, and from the soil
surface after the waste has been tilled into the soil or retilled after
initial waste application.
     Short-term emissions of organics from hazardous waste on the soil
surface prior to tilling, a result of surface application land treatment,
or immediately following tilling, are estimated by calculating an overall
mass transfer coefficient similar to that for an oil film on a surface
impoundment.  The basic assumption is that mass transfer is controlled by
the gas-phase resistance.  The gas-phase mass transfer coefficient and the
equilibrium constant are calculated from the correlation of MacKay and
Matasugu8 and from Raoult's law, respectively.
     The RTI land treatment model is used to calculate emissions from waste
that is mixed with the soil.  This condition may exist when waste has been
applied to the soil surface and has seeped into the soil, when waste has
been injected beneath the soil surface, or when the waste has been tilled
into the soil.  In land treatment, soil tilling typically occurs regardless
of the method of waste application.  Air emissions from  land treatment
operations are at their highest when a waste containing  volatile organics
is applied onto or tilled into the soil or retilled after initial waste
application.  Within a few  hours after application or tilling, the  rate  of
air emissions will be substantially less than the maximum because the
volatiles at the surface have been removed and the remaining volatiles must
diffuse up through a layer  of porous solids.  The effect of tilling on
emissions is reflected in the model by including a short-term maximum
evaporation rate immediately after tilling occurs, then  applying or
resuming the long-term emission  rate model.
     The RTI land treatment emission model for long-term emissions  from  a
land treatment unit incorporates terms that consider the major competing
pathways for loss of organics from the soil; the model  combines  a diffusion
equation for the waste vapors in the soil and a biological  decay rate  equa-
tion.  The RTI model is based on Pick's second law of diffusion  applied  to
                                    C-9

-------
 a flat slab as described by Crank^ and includes a term to estimate biologi-
 cal decay assuming a decay rate that is first order with respect  to waste
 loading in the soil.  No equations are presented here because they are not
 easily condensed.   However, these equations are described in  the  TSDF  air
 emission models report.
      C.I.1.3  Waste Fixation,  Wastepiles,  and Landfills.  Two major
 emission models are used in estimating emissions from landfills.   Both
 assume that all wastes are fixed wastes and that no biological  degradation
 takes place to reduce organic  content.
      One model  estimates emissions from closed landfills.10   The  Closed
 Landfill  Model  is  used to estimate emissions from waste placed  in a closed
 (or capped)  landfill  that is vented to the atmosphere and, as a special
 case,  emissions from active landfills  receiving daily earth covers.  This
 model  accounts  for the escape  of organics  resulting from diffusion  through
 the cap and  convective loss from landfill  vents resulting from  barometric
 pumping.   The  closed  landfill  model  is based primarily on the work  of
 Farmer et al.,11 who  applied Pick's  first  law for steady-state  diffusion.
 Farmer's  equation  utilizes  an  effective diffusion coefficient for the  soil
 cap  based on the work  of Millington  and Quirk.12  The model also  includes a
 step to estimate convective losses  from the landfill.   The TSDF air  emis-
 sion models  report  describes the model  in  detail.
     The  RTI land  treatment model  is used  to estimate the air emissions
 from active  landfills  (landfills  still  receiving wastes)  and  wastepiles.13
 As previously stated,  this  model  is  based  on  Fick's  second law  of diffusion
 applied to a flat  slab as described  by  Crank,  and  it  includes a term to
 estimate  biological decay assuming a decay  rate that  is  first order  with
 respect to waste loading  in the  soil.   A land-treatment-type  model was
 selected  for estimating emissions from  open  landfills  and wastepiles
 because (1) there are  a number of similarities  in physical characteristics
 of open landfills,  wastepiles,  and land treatment operations,  and  (2)  the
 input parameters required for the land  treatment model are generally
 available for open landfills and wastepiles, which  is  not the case for some
of the more theoretical models  for these sources.
     The emission model developed to characterize organic air emissions
from uncovered wastes described in the air emissions model report was not
                                   C-10

-------
considered appropriate for estimating emissions from waste fixation
processes.  However, a number of field tests have been conducted,^ and
these data were used to develop an emission factor for this process.
     C.I.1.4  Transfer, Storage, and Handling.  This subsection discusses
organic emission models for container loading and spills,  fixed-roof tank
loading and storage, dumpster storage, and equipment leaks.
     C.I.1.4.1  Container loading and spills.  Containers  can include
drums, tank trucks, railroad tank cars, and dumpsters.  To calculate organ-
ic emissions from loading liquid wastes into all of these  containers except
dumpsters, the AP-42 equation for loading petroleum liquids is applied.15
This equation was derived for tank cars and marine vessels.  It is also
applied to tank trucks and 0.21-m3 (55-gal) drums in this  case because the
loading principles are similar.  (No equation has been developed exclu-
sively for small containers such as drums.)  Covered container loading
emissions are based on the AP-42 equation:
                                                                      (C-6)
where
     LL  =  loading loss, lb/1,000 gal of liquid loaded
      T  =  bulk temperature of liquid, K
      S  =  saturation factor, dimensionless
      M  =  molecular weight of vapor, Ib/lb mol
      P  =  true vapor pressure of liquid, psia.
     Spillage is the only other significant emission source from covered
containers.  An EPA study of truck transport to and from TSDF and truck
emissions at TSDF terminals provided the background information necessary
to estimate spillage losses during TSDF trucking, handling, and storage
operations.  The emission estimate for losses at a storage facility applies
the same spill fraction used for drum handling, 1 x 10~4, developed by
EPA.16 .The following equation estimates drum handling and storage emis-
sions:
                                 ,-4
                                    x T x
(C-7)
                                   C-ll

-------
 where
      Ls  =  emissions from drum storage,  Mg/yr
       T  ~  throughput,  Mg/yr
      W-j  =  organic weight fraction
      V-j  *  volatilization fraction.
      Spillage  emissions  from tank  trucks  and  railroad  tank  cars  are  esti-
 mated using  the  same equation except  that the spill  fraction  of  10~5 for
 other types  of waste movement is applied  instead  of  the  10~4  spill fraction
 for drum  handling.1?  (See the TSDF air emission  models  report,  Section
 7.7.)
      C.I.1.4.2  Dumpster storage.   Emissions  from open dumpster  storage are
 estimated  using  a model  based originally  upon the work of Arnold, which was
 subsequently modified  by SheniS and EPA/GCA1^ Corporation to  characterize
 organic air emissions  from uncovered wastes.   The equation  in  its final
 form  is thus presented as:
Ei =
                                        ri w
                                   RT
where:
(C-8)
      E-j = emission rate of constituent of interest from the emitting
           surface, g/s
      P0 s total system pressure (ambient pressure), mmHg
     MW-j = molecular weight of constituent i, g/g mol
     y-j* = equilibrium mole fraction of the i-th constitutent in the gas
           phase
       w = width of the volatilizing surface perpendicular to the wind
           direction,  cm
       R - ideal gas constant,  62,300 mmHg»cm3/g mol»K
       T = ambient temperature,  K
      D-i = diffusivity of volatilizing constituent in air,  cm2/s
       1 =? length of volatilizing surface parallel to the wind direction
           cm
                                   C-12

-------
       U = windspeed,  cm/s
      Fv = correction factor for Pick's law
       •K = 3.1416.
     C.I. 1.4. 3  Tank storage.  Stationary,  fixed-roof tank working  losses
are those created by loading and unloading  wastes and are estimated using
AP-42, "Storage of Organic Liquids":20
            Lw = 1.09 x 10
                                "8
                                   x My x P x V x Kn x Kc
 (C-9)
where
     Lw  =  working losses, Mg/yr (the AP-42 constant of 2.4 x 10"2 is
            converted to 1.09 x 10~8 to convert Ib/gal throughput to Mg/yr)
     Mv  =  molecular weight of vapor in tank,  Ib/lb mol
      P  =  true vapor pressure at bulk liquid  conditions,  psia
      V  =  throughput, gal/yr
     Kn  =  turnover factor, dimensionless
     Kc  =  product factor, dimensionless.
     There are also "breathing" losses for a fixed-roof tank caused by
temperature and pressure changes.  An existing  AP-422^ equation is used to
estimate these emissions:
Lb = 1.02 x 10
                    "5
                       M
[  14 P p]  o.
^xD^xH^xAT0'5
(C-10)
           x F  x C x KC
where
     Lt,  =  fixed-roof breathing loss, Mg/yr (the AP-42 constant of 2.26 x
            10"2 is converted to 1.02 x 10~5 to convert Ib/gal thoughput to
            Mg/yr)
     Mv  =  molecular weight, Ib/lb mol
      P  =  true vapor pressure, psia
      D  =  tank diameter, ft
      H  =  average vapor space height, ft
                                   C-13

-------
      AT  s  average ambient diurnal temperature change, °F
      Fp  =  paint factor, dimensionless
       C  =  adjustment factor for small diameter tanks, dimensionless
      Kc  =  product factor, dimensionless.
 These equations originally were developed for handling organic liquids in
 industries producing or consuming organic liquids,  but are used here for
 TSDF tank storage.
      C.I.1.4.4  Equipment leaks.  Emissions from equipment leaks are those
 resulting from leaks in equipment that is used to control  pressure,  provide
 samples,  or transfer pumpable organic hazardous waste.  The emissions from
 equipment leaks in hazardous waste management are dependent on the number
 of pump seals,  valves,  pressure relief devices,  sampling connections, open-
 ended lines,  and the volatility of the wastes handled.  The emission-
 estimating  model used  for TSDF equipment leaks is  independent of the
 throughput,  type,  or size of the process unit.  The TSDF equipment leak
 emission  model  is  based on the Synthetic Organic Chemical  Manufacturing
 Industries  (SOCMI)  emission  factors  developed to support standard SOCMI
 equipment leak  emission standards.22  The input  parameters required  for  the
 equipment leak  emission model  begin  with the  emission  factor for the equip-
 ment  pieces  such as  pump  seals,  the  number of sources,  and the residence
 time  of the waste  in the  equipment.   It  was assumed that with no purge of
 waste from the  equipment  when  the  equipment is not  in  use,  organics  are
 continuously being  leaked to the atmosphere.   Section  C.2,  "Model  Unit
 Description," explains  the selection process  for the number of emission
 sources used to develop the equipment model units.
 C.I.2 Comparison of Emission  Estimates  with  Test Results
      Predictions from TSDF emission models have  been compared with field
 test  data.  The following  sections summarize  qualitatively  the comparative
 results that are discussed in detail in  Chapter 8.0  of the  TSDF air  emis-
 sion models report.  Actual field test data are  presented  in  Appendix  F.
 This comparison was made with the knowledge that some uncertainty  in  field
 test precision  and accuracy and the empirical   nature of emission models
must be considered.
                                   C-14

-------
     C.I.2.1  Surface Impoundments and Uncovered Tanks Comparison.   Emis-
sion test data were available for five quiescent surface impoundments.   The
overall mass transfer coefficients determined in these tests agreed within
an order of magnitude with the overall coefficient predicted by the mass
transfer correlations.  Predicted emissions for these impoundments  using
the March 1987 version of the air emission models were higher than  the
measured emissions in some cases and lower in others.
     When predicted emission estimates were compared to uncovered tank
measured emissions, the results were mixed.  For quiescent tanks, the
predicted emissions were generally lower than measured emissions but agreed
within an order of magnitude.  For the aerated systems, the model predic-
tions agreed well with material balance and ambient air measurements for an
open aerated system.
     C.I.2.2  Land Treatment.  Field test data from four sites and one
laboratory simulation were used as a basis of comparison with estimates
from the land treatment emission model (see Section C.I.1.2).  Estimated
and measured emissions were within an order of magnitude.  Estimates of
both emission flux rates and cumulative emissions show results above and
below measured values.  Considering the potential for error in measuring or
estimating values for input parameters, differences in the range of an
order of magnitude are not unexpected.  The emission test reports did not
provide complete sets of model input data; therefore, field data averages,
averages from the TSDF data base, or values identified elsewhere as repre-
sentative were used as model inputs.
     C.I.2.3  Landfills and Wastepiles.  Comparisons between predicted and
measured emissions from a landfill are of  limited value because of lack of
detailed, site-specific soil, waste, and landfill operating parameters.
Typically, the composition of the landfilled waste.and other required
inputs to the emission models, such as the porosity of the  landfill cap and
the barometric pumping rate, were not included  in the field test data.
Comparisons of model emissions were made to measured emissions from two
active landfills.  The modeled emissions were found to be higher than field
test measurements, in general, by factors  ranging from 1 to 2 orders of
magnitude.  No test data were available for wastepiles.
                                   C-15

-------
                 C.I.2.4  Transfer, Storage, and Handling Comparison.  Emission models
             for transfer, storage, and handling operations are based on extensive
             testing that led to AP-4223 emission models and to models developed for the
             petroleum  industry and SOCMI.  The following models were developed in the
             petroleum  industry and are applied to TSDF:
                 •     Container loading (AP-42, Section 4.4)
                 •     Stationary covered tank loading-(AP-42, Section 4.3)
                 •     Stationary covered tank storage (AP-42, Section 4.3).
                 Equipment leak emission factors are drawn from the study of organics
             leak control at SOCMI facilities.  Test data supporting the SOCMI equipment
             leak emission standard24 were collected to develop these factors.  An EPA
            study2^ of truck transport to and from TSDF and truck emissions at TSDF
            terminals provided information for spillage loss estimates.   No test data
            were available for comparison in this TSDF effort.
            C.I.3   Sensitivity Analysis
                The emission models  have been  evaluated to determine which parameters
            have the greatest impacts  on  emissions.   A brief discussion  follows on the
            important model  parameters for the  four major types of TSDF  processes:  (1)
            surface impoundments  and  uncovered  tanks,  (2)  land treatment,  (3) landfills
            and wastepiles,  and (4) transfer, storage, and handling operations.  Input
            parameters  were  varied  individually over the entire range of  reasonable
            values  in order  to  generate emission  estimates.   A full discussion of the
            emission model sensitivity analysis  is  presented  in the TSDF  air emission
            models  report.
                C.I.3.1  Surface Impoundments  and  Uncovered  Tanks.  Parameters to
            which emission estimates are most sensitive  include waste concentration,
            retention time, windspeed  for  quiescent  systems,  fetch to depth,  and
            biodegradation.
                The emission estimates for highly volatile constituents  (as  defined  in
            Appendix D, Section D.2.3.3.1) are sensitive to short  retention  times.  For
            retention times on the order of several  days,  essentially all  high  vola-
            tiles are emitted.  In impoundments, significant emissions of  medium  vola-
            tiles (as defined in Appendix D, Section D.2.3.3.1) may occur  over  long
_
                                              C-16

-------
retention times.  Henry's law constant has a direct effect on emissions of
medium volatiles and a greater effect on relatively low volatile organics
for which mass transfer is controlled by the gas-phase resistance.
     Temperature did not affect emission estimates of' the highly volatile
constituents, although mass transfer for low volatile constituents was
affected because of the temperature dependence of Henry's law constant.
Diffusivity in air and water did not affect emission estimates.
     Physical parameters of aerated systems, such as kilowatts (horsepower)
and turbulent area, did affect emission estimates of medium volatiles,
although highly volatile constituents were unaffected.  High volatiles are
stripped out almost completely under any aerated condition.
     C.I.3.2  Land Treatment.  Air emissions from land treatment units are
dependent on the chemical/physical properties of the organic constituents,
such as vapor pressure, diffusivity, and biodegradation rate.
     Operating and field parameters affect the emission rate, although
their  impact is not as great as that of constituent properties.  Tilling
depth, for example, plays a role; the deeper the tilling depth, the greater
the time required for diffusion to the surface and therefore the greater  is
the potential for organics to be biodegraded.  Waste concentration and
waste  loading (the amount of material applied to the soil per unit area)
affect the emission rate on a unit area basis (emissions per unit area),
but not in terms of the mass of organics disposed of  (emissions per unit
mass of waste).
     C.I.3.3  Landfills and Wastepiles.  Emissions from active  (open)
landfills, those still receiving wastes, are estimated by applying the RTI
land treatment model.  The sensitivity of the land treatment model to some
parameters differs in  its application to open landfills and wastepiles from
that in land treatment operations.   For application to open  landfills and
wastepiles,  the model  is sensitive to the air porosity of the  solid waste,
the liquid loading in  the solid waste, the waste depth, the  concentration
of the constituent in  the waste,  and the  volatility of the constituent
under  consideration.   In contrast, the model  is  less  sensitive  to the
diffusion coefficient  of the constituent  in  air.
     Emissions  from closed  landfills, those  filled to design  capacity and
with a cap  (final  cover)  installed,  are estimated  using the  closed  landfill
                                    C-17

-------
 model.  The model  is highly sensitive to the air porosity of the clay cap,
 which largely determines the diffusion rate through the cap.  The model is
 also sensitive to  the properties of the constituent of interest, particu-
 larly vapor pressure, Henry's law constant, and concentration.  In con-
 trast, the model exhibits relatively low sensitivity to the diffusiveness
 of the constituent in air, the cap thickness, and the total mass of
 constituent in the landfill.
      C.I.3.4  Transfer. Storage, and Handling Operations.   Equipment leak
 emission estimates are a function of the number of pump seals, valves,
 pressure-relief valves, open-ended lines,  and sampling connections selected
 for given process rather than throughput rate.   However,  equipment leak
 frequencies and leak rates have been shown to vary with stream volatility;
 emissions for high-volatility streams are  greater than those for streams  of
 low volatility.
      Loading emission estimates  are also sensitive to the  volatility of the
 constituents.   Both loading  and  spill  emissions  are directly proportional
 to throughput.   The loading  emission estimates  for open aqueous  systems,
 such  as  impoundments  and uncovered  tanks,  are highly sensitive to  the type
 of-loading,  which is  either  submerged  or splash  loading.
      The  fraction of  waste spilled  and waste  throughput are used to
 estimate  emissions  resulting  from spills.
 C.2   MODEL  TSDF WASTE MANAGEMENT UNIT ANALYSES
      To evaluate  the  effectiveness  (emission  reductions) and  costs of
 applying various  types  of control technologies  (discussed  in  Chapter 4.0)
 to reduce emissions from waste management process units, a model unit anal-
ysis was performed.   Hazardous waste management model  units and  model waste
 compositions were input  to the emission models discussed above to generate
 uncontrolled emissions estimates  from which emission reductions  were  com-
puted.  The model units  and model waste compositions also served as  the
bases for estimating  add-on and suppression-type control costs for each
applicable control technology.  Appendix H presents a discussion of the
costing of add-on and suppression-type controls.
     The development of.model units, selection of model waste compositions
and the results of the analyses of emission reductions and control  costs
are discussed in the following sections.
                                   C-18

-------
C.2.1  Model Unit Descriptions
     Sets of model units were developed to represent the range of sizes and
throughputs of hazardous waste management processes.  For each model  unit,
parameters needed as input to the emission models were specified.  The
following paragraphs provide the sources of information and rationale used
in developing the model units.  Discussions are presented as four categor-
ies, each containing waste management processes with similar emission char-
acteristics.
     Multiple model units were developed for each waste management process
to describe the nationwide range of characteristics (surface area,, waste
throughputs, retention time, etc.).  This was determined using the
frequency distributions of quantity processed, unit size, or unit area of
each waste management process that were results of the Westat Survey.  The
distributions (expressed as weighting factors for the SAM) are presented
with the tabular listing of model units in this section.  The distributions
were used to develop a "national average model unit" to represent each
waste management process when using the Source Assessment Model.  Each
frequency serves as a weighting factor to approximate a national distri-
bution of the model units defined for a particular TSDF waste management
process.  Appendix D, Section D.2.4.3, describes these weights and the
approach to estimating nationwide organic air emissions in greater detail.
     C.2.1.1  Surface Impoundments and Uncovered Tanks.  Hazardous waste
surface impoundment storage, treatment, and disposal model units are dis-
played in Table C-l.  The ranges of surface areas and depths were based on
results of the National Survey of Hazardous Waste Generators and Treatment,
Storage, and Disposal Facilities Regulated Under RCRA in 1981  (Westat
Survey).26  The median surface area for storage and treatment  impoundments
in the Westat Survey was 1,500 m2 and the median depth was 1.8 m.  Three
model unit surface areas and depths were chosen for storage and  treatment
impoundments, representing the medians and spanning the representative
ranges of sizes for each parameter.  The Westat Survey data summary  for
impoundments indicated that disposal impoundments generally have higher
surface areas and shallower depths than storage and treatment  impoundments.
The model disposal impoundment was designed with the Westat Survey median
surface area of 9,000 m2 and the median depth of approximately  1.8 m.
                                   C-19

-------
               TABLE C-l.  DESIGN AND OPERATING PARAMETERS OF
                   HAZARDOUS WASTE SURFACE IMPOUNDMENT AND
                         UNCOVERED TANK MODEL UNITS3
    Model unit (weights,13 %)
        Parameters0
 Surface impoundment storage

    S04A   Quiescent impoundment
    S04B   Quiescent impoundment
    (S04A  and  B = 38.3)

    S04C    Quiescent  impoundment
   S04D   Quiescent  impoundment
   (S04C and D = 35.9)
 Throughput - 99,000 Mg/yr
 Surface area - 300 m2
 Depth - 0.9 m
 Volume - 270 m3
 Retention time -  1 d
 Flow rate - 3.1 L/s
 Temperature - 25  °C
 Windspeed - 4.5 m/s

 Throughput - 9,800 Mg/yr
 Surface area - 300 m2
 Depth - 0.9 m
 Volume - 270 m3
 Retention time -  10 d
 Flow rate - 0.31  L/s
 Temperature - 25  °C
 Windspeed - 4.5 m/s
Throughput  - 49,000 Mg/yr
Surface area -  1,500 m2
Depth - 1.8 m
Volume - 2,700  m3
Retention time  - 20 d
Flow rate - 1.6 L/s
Temperature - 25 °C
Windspeed - 4.5 m/s

Throughput - 25,000 Mg/yr
Surface area -  1,500 m2
Depth - 1.8 m
Volume - 2..700 m3
Retention time - 40 d
Flow rate - 0.78 L/s
Temperature - 25 °C
Windspeed - 4.5 m/s
See notes at end of table.
                      (continued)
                                   C-20

-------
              TABLE C-l.  DESIGN AND OPERATING PARAMETERS OF
                  HAZARDOUS WASTE SURFACE IMPOUNDMENT AND
                  UNCOVERED TANK MODEL UNITS3 (continued)
   Model unit (weights,b %)
       Parameters0
Surface impoundment storage (con.)
   S04E   Quiescent impoundment
   S04F   Quiescent impoundment
   (S04E and F = 25.9)
          y
Surface impoundment treatment

   T02A   Quiescent impoundment with
          no biodegradation
   T02B   Quiescent  impoundment with

          no biodegradation
    (T02A and B = 31.2)
Throughput - 120,000 Mg/yr
Surface area - 9,000 m2
Depth - 3.7 m
Volume 33,000 m3
Retention time - 100 d
Flow rate - 3.8 L/s
Temperature - 25 °C
Windspeed - 4.5 m/s

Throughput - 67,000 Mg/yr
Surface area - 9,000 m2
Depth - 3.7 m
Volume - 33,000 m3
Retention time - 180 d
Flow rate - 2.1 L/s
Temperature - 25 °C
Windspeed - 4.5 m/s
Throughput - 200,000 Mg/yr
Surface area - 300 m2
Depth - 0.9 m
Volume - 270 m3
Retention time - 0.5 d
Flow rate - 6.3 L/s
Temperature - 25 °C
Windspeed - 4.5 m/s

Throughput - 20,000 Mg/yr

Surface area - 300 m2
Depth - 0.9 m
Volume - 270 m3
Retention time - 5 d
Flow rate - 0.63 L/s
Temperature - 25 °C
Windspeed - 4.5 m/s
See notes at end of table.
                       (continued)
                                    C-21

-------
                TABLE C-l.   DESIGN  AND OPERATING  PARAMETERS  OF
                    HAZARDOUS  WASTE SURFACE  IMPOUNDMENT  AND
                    UNCOVERED  TANK  MODEL  UNITS9  (continued)
    Model  unit  (weights,b %)
        Parameters0
 Surface  impoundment treatment  (con.)

    T02C   Quiescent impoundment with
           no biodegradation
    T02D   Quiescent impoundment with
           no biodegradation
    (T02C and D = 35.6)

    T02E   Quiescent impoundment with

           no biodegradation
   T02F   Quiescent  impoundment with
          no biodegradation
   (T02E and F = 33.3)
 Throughput - 990,000 Mg/yr
 Surface area - 1,500 m2
 Depth - 1.8 m
 Volume - 2,700 m3
 Retention time -Id
 Flow rate - 31 L/s
 Temperature - 25 °C
 Windspeed - 4.5 m/s

 Throughput - 99,000 Mg/yr
 Surface area - 1,500 m2
 Depth - 1.8 m
 Volume - 2,700 m3
 Retention time - 10 d
 Flow rate - 3.1 L/s
 Temperature - 25 °C
 Windspeed - 4.5 m/s
 Throughput  -  608,000  Mg/yr

 Surface  area  - 9,000  m2
 Depth  -  3.7 m
 Volume - 33,000 m3
 Retention time - 20 d
 Flow rate - 19 L/s
 Temperature - 25 °C
 Windspeed - 4.5 m/s

 Throughput - 302,000 Mg/yr

 Surface  area - 9,000 m2
 Depth  -  3.7 m
 Volume - 33',000 m3
 Retention time - 40 d
 Flow rate - 9.6 L/s
Temperature - 25 °C
Windspeed - 4.5 m/s
See notes at end of table.
                      (continued)
                                   C-22

-------
              TABLE C-l.  DESIGN AND OPERATING PARAMETERS OF
                  HAZARDOUS WASTE SURFACE IMPOUNDMENT AND
                  UNCOVERED TANK MODEL UNITS3 (continued)
   Model unit (weights,b %)
       Parameters0
Surface impoundment treatment (con.)

   T02G   Aerated/agitated impoundment
          with biodegradation
   T02H   Aerated/agitated impoundment
          with biodegradation
    (T02G and  H  = 31.2)
Throughput - 200,000 Mg/yr
Surface area - 300 m2
Depth - 0.9 m
Volume - 270 m3
Retention time - 0.5 d
Flow rate - 6.3 L/s
Turbulent area - 63 m2
Total power - 5.6 kW (7.5 hp)
Impeller power - 4.8 kW (6.4
Impeller speed - 130 rad/s
Impeller diameter - 61 cm
0? transfer - 1.83 kg/kW/h
 13 Ib/hp/h)
02 correction factor
Biomass concentration
Temperature - 25 °C
Windspeed - 4.5 m/s
                                                                      hp)
                                                                0.83
                                                                 0.5 g/L
Throughput - 20,000 Mg/yr
Surface area - 300 m2
Depth - 0.9 m
Volume - 270 m3
Retention time - 5 d
Flow rate - 0.63 L/s
Turbulent area - 63 m2
Total power - 5.6 kW  (7.5 hp)
Impeller power - 4.8  kW  (6.4 hp)
Impeller speed - 130  rad/s
Impeller diameter - 61 cm
0? transfer - 1.83 kg/kW/h
 13 Ib/hp/h)
02 correction factor  - 0.83
Biomass concentration -  0.5 g/L
Temperature. - 25 °C
Windspeed - 4.5 m/s
 See  notes  at  end of  table.
                       (continued)
                                    C-23

-------
               TABLE C-l.   DESIGN  AND  OPERATING  PARAMETERS OF
                   HAZARDOUS WASTE SURFACE  IMPOUNDMENT AND
                   UNCOVERED TANK  MODEL  UNITS3  (continued)
    Model unit  (weights,b %)
                                       Parameters0
 Surface impoundment treatment  (con.)


    T02I   Aerated/agitated impoundment   Throughput  -  990,000 Mg/yr
           t«i*i T* h r\T^\rt^^/^w\^*J^^^**»^            r*..	c___  _____    "t  *•*>**   O
           with biodegradation
    T02J
Aerated/agitated  impoundment
with biodegradation
 Surface area - 1,500 m
 Depth - 1.8 m
 Volume - 2,700 m3
 Retention time - 1 d
 Flow rate - 31 L/s
 Turbulent area - 370 m2
 Total  power - 56 kW (75 hp)
 Impeller power - 48 kW (64 hp)
 Impeller speed - 130 rad/s
 Impeller diameter - 61 cm
 0?  transfer - 1.83 kg/kW/h
  (3 Ib/hp/h)
 02  correction factor - 0.83
 Biomass concentration - 0.5  g/L
 Temperature - 25 °C
 Windspeed - 4.5  m/s

 Throughput  -  99,000 Mg/yr
 Surface area  - 1,500 m^
 Depth  - 1.8 m
 Volume  -  2,700 m3
 Retention time - 10 d
 Flow rate - 3.1  L/s
 Turbulent area - 370 m2
 Total power - 56 kW (75 hp)
 Impeller  power - 48 kW (64 hp)
 Impeller  speed - 130 rad/s
 Impeller  diameter  - 61  cm
0? transfer -  1.83  kg/kW/h
 (3 Ib/hp/h)
02 correction  factor -  0.83
Biomass concentration  -  0.5 g/L
Temperature -  25 °C
Windspeed - 4.5  m/s
   (T02I and J = 35.6)
See notes at end of table.
                                                     (continued)
                                   C-24

-------
              TABLE C-l.  DESIGN AND OPERATING PARAMETERS OF
                  HAZARDOUS WASTE SURFACE IMPOUNDMENT AND
                  UNCOVERED TANK MODEL UNITS3 (continued)
   Model unit (weights,b %)
       Parameters0
Surface impoundment treatment (con.)

   T02K   Aerated/agitated impoundment
          with biodegradation
   T02L   Aerated/agitated impoundment
          with biodegradation
   (T02K and L = 33.3)

Surface impoundment disposal

   D83A   Quiescent impoundment with
          no biodegradation (100)
Throughput - 608,000 Mg/yr
Surface area - 9,000 m2
Depth - 3.7 m
Volume - 33,000 m3
Retention time - 20 d
Flow rate - 19 L/s
Turbulent area - 2,700 m2
Total power - 671 kW (900 hp)
Impeller power - 574 kW (85 hp)
Impeller speed - 130 rad/s
Impeller diameter - 61 cm
0? transfer - 1.83 kg/kW/h
 13 Ib/hp/h)
02 correction factor - 0.83
Biomass concentration - 0.5 g/L
Temperature - 25 °C
Windspeed - 4.5 m/s

Throughput - 302,000 Mg/yr
Surface area - 9,000 m2
Depth - 3.7 m
Volume - 33,000 m3
Retention time - 40 d
Flow rate - 9.6 L/s
Turbulent area - 2,700 m2
Total power - 671 kW (900 hp)
Impeller power - 574 kW (85 hp)
Impeller speed - 130 rad/s
Impeller diameter - 61 cm
0? transfer - 1.83 kg/kW/h
 (3 Ib/hp/h)
02 correction factor - 0.83
Biomass concentration - 0.5 g/L
Temperature - 25 °C
Windspeed - 4.5 m/s
Throughput - 32,000 Mg/yr
Surface area - 9,000 m2
Depth - 1.8 m
Volume - 16,000 m3
See notes at end of table.
                       (continued)
                                   C-25

-------
                TABLE C-l.   DESIGN AND OPERATING PARAMETERS OF
                    HAZARDOUS WASTE SURFACE IMPOUNDMENT AND
                    UNCOVERED TANK MODEL UNITS9 (continued)
     Model  unit (weights,13 %)
        Parameters0
  Surface  impoundment  disposal  (con.)
 Storage tanks

    S02F   Uncovered tank  (37.7)
    S02G   Uncovered tank (Od)
    S02H   Uncovered tank (32.3)
    S02I    Uncovered tank (17.8)
   S02J   Uncovered tank  (12.2)
See notes at end of table.
                                           Retention  time -  183  d
                                           Temperature  -  25  °C
                                           Windspeed  -  4.5 m/s
 Throughput - 110 m3/yr
 Surface area - 2.3 m2
 Depth - 2.4 m
 Volume - 5.3 m3
 Retention time - 18.3 d
 Temperature - 25 °C
 Windspeed - 4.5 m/s

 Throughput - 60 m3/yr
 Surface area - 13 m2
 Depth - 2.4 m
 Volume - 30 m3
 Retention time - 183 d
 Temperature - 25 °C
 Windspeed - 4.5 m/s

 Throughput - 1,100  m3/yr
 Surface area - 13 m2
 Depth - 2.4 m
 Volume - 30 m3
 Retention time - 9.9 d
 Temperature - 25 °C
 Windspeed - 4.5 m/s

 Throughput -  3,300  m3/yr
 Surface  area  -  26 m2
 Depth  -  2.7 m
 Volume  -  76. m3
 Retention  time  -  8.3  d
 Temperature -  25  °C
 Windspeed  - 4.5 m/s

 Throughput  -  17,000 m3/yr
 Surface area  -  65 m2
 Depth - 12 m
 Volume - 800 m3
 Retention time  -  17.4 d
Temperature - 25  °C
Windspeed - 4.5 m/s
                                   C-26
                      (continued)

-------
              TABLE C-l.  DESIGN AND OPERATING PARAMETERS OF
                  HAZARDOUS WASTE SURFACE IMPOUNDMENT AND
                  UNCOVERED TANK MODEL UNITSa (continued)
   Model unit (weights,13 %)
                                      Parameters0
Treatment tanks
   T01A
Uncovered quiescent tank
(28.3)
   T01B
Uncovered quiescent tank
(21.8)
   T01C
Uncovered quiescent tank
(50.0)
   T01G
Uncovered aerated/agitated
tank (78.3)
Throughput - 11,000 Mg/yr
Surface area - 13 m2
Depth - 2.4 m
Volume - 30 m3
Retention time - 24 h
Flow rate - 0.35 L/s
Temperature - 25 °C
Windspeed - 4.5 m/s

Throughput - 28,000 Mg/yr
Surface area - 26 m2
Depth - 2.7 m
Volume - 76 m3
Retention time - 24 h
Flow rate - 0.88 L/s
Temperature - 25 °C
Windspeed - 4.5 m/s
                     Mg/yr
Throughput - 290,OOC
Surface area - 65 m^
Depth - 12 m
Volume - 800 m3
Retention time - 24
Flow rate - 9.2 L/s
Temperature - 25 °C
Windspeed - 4.5 m/s
Throughput - 240,000 Mg/yr
Surface area - 27 m2
Depth -4m
Volume - 108 m3
Retention time
Flow rate - 7.5 L/s
Turbulent area - 14 m2
Total power - 5.6 kW (7
Impeller power - 4.8 kW
Impeller speed
                                                        - 4 h
                                                                 5 hp)
                                                                 (6.4 hp)
                                                          130 rad/s
                                         Impeller diameter - 61 cm
                                         0? transfer - 1.83 kg/kW/h
                                           (3 Ib/hp/h)
                                         02 correction factor - 0.83
                                         Biomass concentration - 4.0  g/L
                                         Temperature - 25 °C
                                         Windspeed - 4.5 m/s
                                   C-27
                                                                (continued)

-------
               TABLE C-l.  DESIGN AND OPERATING PARAMETERS OF
                   HAZARDOUS WASTE SURFACE IMPOUNDMENT AND
                   UNCOVERED TANK MODEL UNITS9 (continued)
    Model unit (weights,b %)
        Parameters0
 Treatment tanks (con.)

    T01H   Uncovered aerated/agitated
           tank (21.8)
Throughput - 2,800,000 Mg/yr
Surface area - 430 m2
Depth - 3.7 m
Volume - 1,600 m3
Retention time - 5 h
Flow rate - 88 L/s
Turbulent area - 250 m2
Total power - 89.5 kW
 (120 hp)
Impeller power - 38 kW (51 hp)
Impeller speed - 130 rad/s
Impeller diameter - 61 cm
0? transfer - 1.83 kg/kW/h
 (3 Ib/hp/h)
Og correction factor - 0.83
Biomass concentration - 4.0 g/L
Temperature - 25 °C
Windspeed - 4.5 m/s
 Hazardous waste  surface  impoundment  and  uncovered  tank model  units  repre-
  sent the ranges  of  uncovered,  quiescent,  and  aerated  surface  storage,
  treatment,  and disposal  surface  impoundments  and storage  and  treatment
  tanks  in the  hazardous waste management  industry.

 bBecause design characteristics and operating  parameters (surface area,
  waste  throughputs,  detention times,  and  so on) were generally not avail-
  able for all  treatment,  storage, and disposal facilities  (TSDF),
  weighting factors were developed to  approximate the nationwide distri-
  bution of model  units defined  for a  particular TSDF waste management
  process.  The weighting  factors are  based on  the considerable statistical
  data available in the 1981 EPA survey of hazardous waste generators and
  TSDF conducted by Westat, Inc. (Westat Survey).  For example, results of
  this survey were used to determine the national distribution  of sizes of
  storage tanks (storage volume), surface impoundments  (surface area)  and
  landfills (surface  area  and depth).  For further information  on weighting
  factors, refer to Appendix D, Sections D.2.4.3 and D.2.5.

cModel unit parameters may not be equal (e.g., Throughput j4 Volume x
 Turnovers)  because of rounding.

dThis model  unit was weighted 0% because S02H  also has the same surface
 area.  This avoids double weighting of a unit siz,e.
                                   C-28

-------
     Retention times in the Westat Survey ranged from 1 to 550 days,  with
over half of the values at 46 days or less.  The storage impoundment  model
unit retention times, ranging from 1 to 180 days, were chosen to span the   -.
reasonable range of values, based on knowledge of the operation of impound-
ments that are representative of the industry.  Retention times greater
than 180 days were not used to estimate emissions because organics are
emitted from a surface impoundment within 180 days.  The retention time in
treatment impoundments was expected to be less than the retention times in
storage impoundments.  Two design manuals listed typical retention times
for aerated impoundments as 7 to 20 days27 and 3 to 10 days.28  Retention
times bounding these ranges were chosen for the quiescent and aerated/
agitated impoundments.  No data were available concerning disposal surface
impoundment retention times; therefore, the disposal surface  impoundment
was selected with a  6-month retention time or the time within which the
organics would be emitted.  Volume  for each surface impoundment model unit
was calculated from  area and depth; the retention time yielded the flow
rate.
     Two meteorological parameters  required for  the emission  models were
temperature and windspeed.  The parameters chosen were  a  standard tempera-
ture of 25 °C and a  windspeed of  4.5 m/s.  These standard values were eval-
uated by estimating  emissions from  surface impoundments  for windspeed/
temperature combinations  at  actual  sites  based  on  their frequency of
occurrence.   Over a  1-yr  period,  the results  from  site-specific data  on
windspeed  and temperature were  not  significantly different  from the  results
using the  standard  values.   Consequently,  the standard  values were judged
adequate  for  the model  units.
     With  regard to the aerated/agitated  treatment  impoundments,  one
source,  Metcalf  and Eddy,29  suggests a  range  of 0.37  to 0.75  kW/28.3  m3
 (0.5 to 1.0  hp/1,000 ft3)  for mixing.   However,  more  power  may be needed to
supply  additional  oxygen  or  to  mix  certain treatment  solutions.   Informa-
tion obtained through  site visits to impoundments  indicates power usage as
high as 2.6  kW/28.3 m3 (3.5  hp/1,000 ft3) at  a  specific TSDF impoundment.30
 For this analysis,  a midrange value of 0.56  kW/28.3 m3 (0.75 hp/1,000 ft3)
 from Metcalf and Eddy, was used  to generate estimates of the power required
 for mixing in each  model  unit.
                                    C-29

-------
      Data from Reference 31 indicate that an aerator with a 56-kW (75-hp)
 motor and a 61-cm-diameter propeller turning at 126 rad/s would agitate a
 volume of 660 m3.  Agitated volumes were estimated by holding propeller
 diameter and rotation constant and treating agitated volume as being pro-
 portional to power.  The agitated volume divided by depth yielded the agi-
 tated surface area, which was modeled as turbulent area.  Typical values
 were chosen for the oxygen transfer rating of the aerator and the oxygen
 transfer correction factor.  A value of 1.83 kg 02/kW/h (3.0 Ib 02/hp/h)
 was chosen for the oxygen transfer rating from a range of 1.76 to 1.83 (2.9
 to 3.0),32  A value of 0.83 was used for the correction factor from a typi-
 cal range of 0.80 to 0.85.33  For estimating the impeller power,  an
 85-percent efficient transfer of power to the impeller was used.34  A
 midrange biomass  concentration for continuous stirred  tank reactors was
 chosen  from Reference 35.   A biomass concentration of  0.5 g/L was chosen as
 an estimate,  representing  an upper bound on  the design guidelines in
 References  36  and 37.
      Table  C-l  also presents uncovered,  quiescent  and  aerated/agitated
 hazardous waste treatment  tank model  units.   According to responses  to the
 1981  EPA  survey of hazardous waste generators  and  TSDF conducted  by  Westat,
 Inc.  (Westat Survey),38  there  are four  sizes  of tanks  that best  represent
 the waste management  industry:   5.3  m3,  30 m3,  76  m3,  and  800  m3.   The
 quiescent storage and  treatment tank  model units were  sized  accordingly.
      Retention  times were  chosen  to  span the  retention  times  commonly used
 by wastewater treatment  tank units.39  jhe retention times and tank  capaci-
 ties  were used  to arrive at  flow  rates for the  model units.   These flow
 rates are comparable to  those  found  in the EPA  survey  conducted by Westat
 for medium and  large wastewater treatment tanks.   The  remaining physical
 parameters for quiescent treatment tanks were chosen on  the basis of
 engineering judgment.  Meteorological conditions cited for quiescent  and
 aerated tanks represent  standard  annual  (temperature and windspeed) and
 daily (temperature change) values.
     For aerated/agitated treatment tanks, the  agitation parameters for the
 aerated,  biologically active tanks were derived as described previously for
aerated/agitated surface impoundments.
                                   C-30

-------
     C.2.1.2  Land Treatment.  Table C-2 displays hazardous waste land
treatment model units.  Model unit parameters were based primarily on a
data base developed by EPA40 from site visits and contacts with State,
regional, and industry sources and supplemented by information from recent
literature.  These values were chosen as reasonably representative of aver-
age or typical practices currently used at land treatment operations.  The
data base showed annual throughput varying from about 2 Mg/yr to about
400,000 Mg/yr with a median value of 1,800 Mg/yr.  The area of land treat-
ment sites ranged from less than 1 ha to about 250 ha with a median value
of 5 ha.  These two median values were selected to develop the model units.
The data base showed tilling depth varying from 15 cm to one case of 65 cm,
with most being in the range of 15 to 30 cm.  The single most frequently
reported tilling depth was 20 cm, which was  selected as a typical value.
This value is  in line with values of 15 to 30 cm reported in another
study.41  The data base showed oil content of the waste streams  varying
from about 2 to 50 percent, with a median value of about  12 percent  and
model value of 10 percent.  The 10-percent figure was selected as typical.
     Very  little soil porosity information has been  identified.  One  study
reported measured values of  soil porosity in a land  treatment plot  as  rang-
ing from 43.3  to 65.1 percent42 with an average  value of  about 50 percent.
The literature did not specify whether  this  soil porosity represented  total
soil porosity  or soil  air  porosity.  Therefore,  these literature values
were chosen to represent soil air porosity.   Total soil porosity included
the air porosity and  the space occupied by oil and water  within  soil.  One
field study reported  measured values of both total porosity and  air-filled
porosity.43   Measured values of total  soil porosity  ranged  from  54.7 to
64.8 percent,  with  an average value  of  60.7  percent. Measured values of
air-filled porosity  ranged from 27.4 to 46.9 percent, with  an  average of
37.2 percent.  Thus,  the value of 61 percent for total  soil  porosity was
chosen  to  be  a representative value  based  on the median measured total soil
porosity of 60.7  percent.   A value  of  50  percent was used as  a default for
air porosity.
     C.2.1.3   Waste Fixation,  Hastepiles/  and Landfills.   As  part of the
 landfill  operation,  fixation model  units  were developed.   Table  C-3 shows
hazardous  waste  fixation  pit model  units.   The fixation pit has  a length of
                                    C-31

-------
               TABLE C-2.  DESIGN AND OPERATING PARAMETERS OF
                       HAZARDOUS WASTE LAND TREATMENT
                                MODEL UNITS9
    Model unit  (weights,b %)
        Parameters
    D81A    (NA)
    D81B   (NA)
    D81C   (NA)
    D81D    (NA)
 Throughput - 360 Mg/yr
 Land areac - 1  ha
 Oil  content of  waste - 10%
 Soil  air porosity -  0.5
 Soil  total  porosity  - 0.61
 Tilling  depth - 20 cm
 Temperature - 25 °C

 Throughput  - 1,800 Mg/yr
 Land  area0  - 5  ha
 Oil  content of  waste - 10%
 Soil  air porosity -  0.5
 Soil  total  porosity  - 0.61
 Tilling  depth -  20 cm
 Temperature - 25  °C

 Throughput  -  5,400 Mg/yr
 Land  areac  -  15  ha
 Oil content of waste -  10%
 Soil  air  porosity  -  0.5
 Soil  total  porosity  - 0.61
 Tilling depth - 20 cm
 Temperature  - 25  °C

 Throughput  - 27,000  Mg/yr
 Land  areac  - 75 ha
Oil content of waste -  10%
Soil  air porosity  -  0.5
Soil total porosity  - 0.61
Tilling depth -  20 cm
Temperature - 25 °C
NA - Not applicable.

Hazardous waste land treatment model units represent the range of land
 treatment processes in the hazardous waste management industry.

Weighting factors were developed for each unit to represent each waste
 management process when estimating nationwide emissions.  These factors
 are based on frequency distributions of quantity processed, unit size  or
 unit area that were results of the Westat Survey, approximately a national
 distribution of model  units.

cWaste is applied only  to one-half of the land area based on knowledge of
 industry practice, allowing the undisturbed area to stabilize.
                                   C-32

-------
              TABLE C-3.  DESIGN AND OPERATING PARAMETERS OF
             HAZARDOUS WASTE FIXATION PIT,  WASTEPILE STORAGE,
                    AND LANDFILL DISPOSAL MODEL UNITS3
Model unit (weights,b %)
           Parameters
Fixation pit

   Fixation pit A (46.0)
   Fixation pit B  (14.9)
Throughput - 17,000 Mg/yr
 fixed waste
Liquid/fixative - 1 cm3 liquid +
 fixative = 1 cm3 fixed waste
Fixed waste density - 1.8 g/cm3
Number of pits - 1
Pit surface dimensions - 3x6 m
Pit depth -3m
Number of batches - 160/yr
Windspeed - 4.5 m/s
Wind direction - along length of
 pit
Temperature = 25 °C
Duration of fixation - 2 h

Throughput - 120,000 Mg/yr
 fixed waste
Liquid/fixative - 1 cm3 liquid +
 fixative = 1 cm3 fixed waste
Fixed waste density - 1.8 g/cm3
Number of pits - 2
Pit surface dimensions - 3x6 m
Pit depth -3m
Number of batches - 1,200/yr
Windspeed - 4.5 m/s
Wind direction - along length of
 pit
Temperature - 25 °C
Duration of fixation - 2 h
 See notes  at end of table.
                       (continued)
                                    C-33

-------
               TABLE C-3.  DESIGN AND OPERATING  PARAMETERS OF
              HAZARDOUS WASTE FIXATION PIT, WASTEPILE STORAGE,
               AND LANDFILL DISPOSAL MODEL UNITS3  (continued)
 Model unit  (weights,b %)
            Parameters
 Fixation pit (con.)

    Fixation pit C  (39.2)
 Hastepile

    S03D    Wastepile  (41.5)
 Throughput - 170,000 Mg/yr
  fixed waste
 Liquid/fixative - 1 cm3 liquid +
  fixative = 1 cm3 fixed waste
 Fixed.waste density - 1.8 g/cm3
 Number of pits - 4
 Pit surface dimensions - 3x6 m
 Pit depth -3m
 Number of batches - 1,600/yr
 Windspeed - 4.5'm/s
 Wind direction - along length of
  pit
 Temperature - 25 °C
 Duration  of fixation  - 2 h
Throughput -  17,000 Mg/yr
Surface area  - 46 m2
Average height - 0.77 m
Volume - 35 m3
Waste density - 1.8 g/cm3
Turnovers - 300/yr
Retention time - 1.2 days
Temperature - 25 °C
Windspeed - 4.5 m/s
Liquid/fixative - 1 cm3 liquid +
 fixative = 1 cm3 fixed waste
Total porosity fixed waste - 0.50
Air porosity fixed waste - 0.25
Biomass concentration - 0 g/cm3
See notes at end of table.
                      (continued)
                                   C-34

-------
              TABLE C-3.  DESIGN AND OPERATING PARAMETERS OF
             HAZARDOUS WASTE FIXATION PIT, WASTEPILE STORAGE,
              AND LANDFILL DISPOSAL MODEL UNITS3 (continued)
Model unit (weights,b %)
           Parameters
Wastepile (con.)

   S03E   Wastepile (36-.0)
   S03F   Wastepile  (22.5)
Throughput - 120,000 Mg/yr
Surface area - 470 m2
Average height -1m
Volume - 470 m3
Waste density - 1.8 g/cm3
Turnovers - 140/yr
Retention time - 2.6 days
Temperature - 25 °C
Windspeed - 4.5 m/s
Liquid/fixative - 1 cm3 liquid +
 fixative = 1 cm3 fixed waste
Total porosity fixed waste - 0.50
Air porosity fixed waste - 0.25
Biomass concentration - 0 g/cm3

Throughput - 170,000 Mg/yr
Surface area - 14,000 m2
Average height -4m
Volume - 56,000 m3
Waste density - 1.8 g/cm3
Turnovers - 1.6/yr
Retention time - 220 days
Windspeed - 4.5 m/s
Temperature - 25 °C
Liquid/fixative - 1 cm3  liquid +
 fixative = 1 cm3 fixed waste
Total porosity fixed waste - 0.50
Air porosity fixed waste - 0.25
Biomass concentration - 0 g/cm3
 See  notes  at  end  of  table.
                       (continued)
                                    C-35

-------
                TABLE C-3.   DESIGN  AND  OPERATING  PARAMETERS OF
               HAZARDOUS  WASTE  FIXATION PIT,  WASTEPILE  STORAGE
                AND  LANDFILL DISPOSAL MODEL  UNITS9  (continued)
 Model  unit  (weights,b %)
            Parameters
 Landfill disposal

    D80D   Active landfill  (46.0)
    D80E   Active landfill (14.9)
   D80F   Active  landfill  (39.2)
 Surface area - 0.4 ha
 Depth of waste - 1.1 m
 Degree of filling - half full
 Ambient temperature - 25 °C
 Liquid/fixative - 1 cm3 liquid +
  fixative = 1 cm3 fixed waste.
 Total porosity of fixed
  waste - 0.50
 Air porosity of fixed
  waste - 0.25
 Biomass cone. - 0 g/cm3

 Surface area - 1.4 ha
 Depth of waste - 2.3 m
 Degree of filling - half full
 Ambient temperature - 25 °C
 Liquid/fixative - 1 cm3 liquid +
  fixative =  1 cm3 fixed waste
 Total  porosity of fixed
  waste -  0.50
 Air  porosity of fixed
  waste -  0.25
 Biomass cone.  -  0 g/cm3

 Surface area -  2  ha
 Depth  of waste  -  2.3  m
 Degree of  filling  -  half full
 Ambient temperature  - 25 °C
 Liquid/fixative -  1 cm3  liquid +
 fixative  =  1 cm3 fixed waste
 Total porosity of fixed
 waste - 0.50
Air porosity of fixed waste - 0.25
Biomass cone. - 0 g/cm3
See notes at end of table.
                                                               (continued)
                                   C-36

-------
              TABLE C-3.  DESIGN AND OPERATING PARAMETERS OF
             HAZARDOUS WASTE FIXATION PIT, WASTEPILE STORAGE,
              AND LANDFILL DISPOSAL MODEL UNITS3 (continued)
Model unit (weights,13 %)
           Parameters
Landfill disposal (con.)

   D80G   Closed landfill (46.0)
   D80H   Closed landfill  (14.9)
Surface area - 0.4 ha
Waste bed thickness - 2.3 m
Cap thickness - 110 cm
Total porosity of cap - 0.41
Air porosity of cap - 0.08
Temperature beneath cap - 15 °C
Typical barometric pressure -
 1.01 x ID'5 Pa (1,013 mbar)
Daily barometric pressure drop -
 4.0 x 10~8 Pa (4 mbar)
Liquid/fixative - 1 cm3 liquid +
 fixative = 1 cm3 fixed waste
Air porosity of fixed waste -
 0.25
Biomass cone. - 0 g/cm3

Surface area - 1.4 ha
Waste bed thickness - 4.6 m
Cap thickness - 110 cm
Total porosity of cap - 0.41
Air porosity of cap - 0.08
Temperature beneath cap - 15 °C
Typical barometric pressure -
 1.01 x ID'5 Pa (1,013 mbar)
Daily barometric pressure drop -
 4.0 x 10~8 Pa  (4 mbar)
Liquid/fixative -  1 cm3  liquid +
 fixative = 1 cm3  fixed waste
Air  porosity of fixed waste -
 0.25
Biomass cone. - 0  g/cnn
 See notes  at  end  of  table.
                       (continued)
                                    C-37

-------
               TABLE C-3.  DESIGN AND OPERATING PARAMETERS OF
              HAZARDOUS WASTE FIXATION PIT,  WASTEPILE STORAGE
               AND LANDFILL DISPOSAL MODEL UNITS3 (continued)
 Model unit (weights,b %)
            Parameters
 Landfill  disposal  (con.)

    D80I    Closed landfill  (39.2)
Surface area - 2 ha
Waste bed thickness - 4.6 m
Cap thickness - 110 cm
Total porosity of cap - 0.41
Air porosity of cap - 0.08
Temperature beneath cap - 15 °C
Typical barometric pressure -
 1.01 x 10-5 Pa (1,013 mbar)
Daily barometric pressure drop -
 4.0 x ID'8 Pa (4 mbar)
Liquid/fixative - 1 cm3 liquid +
 fixative = 1 cm3 fixed waste
Air porosity of fixed waste -
 0.25
Biomass cone. - 0 g/cm3
Hazardous waste fixation pit, wastepile storage, and landfill disposal
 model units represent the ranges of these processes in the hazardous waste
 management industry.

bBecause design characteristics and operating parameters (surface area
 waste throughputs, detention times, and so on) were generally not avail-
 able for all  treatment, storage, and disposal facilities (TSDF),  weighting
 factors were developed to approximate the nationwide distribution of model
 units defined for a particular TSDF waste management process.  The
 weighting factors are based on the considerable statistical data available
 in the 1981 EPA survey of hazardous waste generators and TSDF conducted by
 Westat,  Inc.  (Westat Survey).  For example,  results of this survey were
 used to determine the national distribution  of sizes of storage tanks
 (storage volume),  surface impoundments (surface area),  and  landfills
 (surface area and depth).  For further information  on  weighting factors
 refer to Appendix D,  Sections D.2.4.3  and D.2.5.
                                  C-38

-------
6 m, with a width of 3 m and a depth of 3 m.   These dimensions represent
reasonable estimates of industry practice based on observations at actual
sites.  The duration of the fixation operation was taken to be a maximum of
2 h, based on operating practice at one site.44  The wind direction was
assumed to be along the length of the pit, and a standard temperature of
25 °C and windspeed of 4.5 m/s were used.
     Hazardous waste wastepile storage model  units are presented in
Table C-3 as part of landfill operations.  The wastepile surface areas were
designed to represent the range of basal areas reported in the Westat
Survey, with 470 m2 being an approximately midrange value.  For modeling
purposes, the pile was assumed to be flat.  The heights were based on
Westat information and engineering judgment.  The wastepile retention times
were derived from the landfill volumes, the wastepile volumes, and the
landfill filling time (to capacity) of  1 yr.  With regard to the waste
characteristics, the waste density represents a fixed two-phase aqueous/
organic waste.  The fixation industry  indicated that waste liquid, when
combined with fixative, may  increase in volume by up to 50 percent,45,46,47
depending on the specific combination  of waste fixative.  However, because
of  the inherent variability  in the fixation process and the lack  of  real
data on volume changes, this analysis  did not  incorporate a waste volume
change during fixation.  Measurements48 performed on various  types of  fixed
waste yielded a broad range  of total porosities;  therefore, 50 percent  was
chosen as a  reasonable estimate  of total  porosity.  A 25-percent  air poros-
ity value was inferred from  measurements  of total porosity and moisture
content.4$   The toxic property of the  waste can  inhibit the biological
processes and prevent biogas generation.50  Therefore,  the waste  biomass
concentration is 0  g/cm^.
      Table  C-3 also provides hazardous waste  landfill disposal model units.
The active  landfill surface  areas  represent the  range of  surface  areas
 reported  in  the  Westat  Survey.   A  standard temperature  of 25  °C was  chosen
 for the model.
      As with active landfills,  the  closed landfill  surface  areas  and depths
were  based  on Westat  Survey  data.   The landfill  cap was considered to be
 composed  of compacted clay.   The cap thickness of 110  cm represents  the
 average  of  extremes in  thickness of clay caps (61 cm to 180  cm)  reported in
                                    C-39

-------
  site  studies.51   The  value  used  for  air  porosity of the clay cap is 8 per-
  cent, while the  total porosity is 41 percent.  These values were computed
  based on  reasonable physical properties  and  level of compaction for
  compacted clay.52  jhe temperature beneath the landfill cap was estimated
  at 15 °C, which  represents  the temperature of shallow ground water at a
  mid-latitude U.S. location.53  A constant temperature was used.  The
  landfill is exposed to a nominal barometric pressure of 1.01 x 10~5 Pa
  (1,013 mbar), which represents an estimate of the annual average atmos-
  pheric pressure  in the United States.54  Barometric pumping was estimated
  for the landfill using a daily pressure drop from the nominal value of
 4.0 x 10-8 Pa (4 mbar).   The 4.0 x 10-8 pa (4 mbar)  value represents an
 estimate of the annual average diurnal  pressure drop.55  jhe closed
 landfill model  units were designed to contain fixed or solid wastes.  As
 explained previously for hazardous waste wastepile model units, biomass
 concentration was taken  to be 0 g/cm3 for active and closed landfills.
      C.2.1.4  Transfer,  Storage,  and  Handling.   Table  C-4 presents  model
 units  for loading and  storing hazardous waste in  containers and covered
 tanks  and for sources  of equipment leaks  during  waste  transfer.  The EPA's
 Hazardous Waste  Data Management  System  was  reviewed56  to select the most
 representative volumetric capacities  of container storage  (drums  and dump-
 sters) facilities.   Based on this review, two model  drum storage  facilities
 were developed:   an onsite or private TSDF with  a 21-m3  capacity  processing
 42 m3  annually, and a  commercial  TSDF with a  40-m3 capacity processing
 460 m3 annually.   The  Westat Survey indicated that waste containers are
 typically  in the  form  of  0.21-m3  (55-gal) drums.57   Therefore,  these model
 capacities would  hold  100 and 180 drums,  respectively, at  any one time.   A
 telephone conversation with  a dumpster  vendor58 identified  two  basic  capa-
 cities of small roll-off  containers:  3.1 m3  and  4.6 m3.   The 3.1-ra3  roll-
 off, which turns  over 6.1 m3 annually,  was selected as a model.   It  has  a
 length of 1.9 m, width of 1.5 m, and  height of 1.2 m.  In  addition,  an
 average annual ambient temperature of 25 °C and an average-windspeed of
 4.5 m/s were used.
     Containers (drums, tank trucks, and rail tank cars) were considered to
be splash-loaded for emission-estimating purposes because data were not
                                   C-40

-------
              TABLE C-4.   DESIGN AND OPERATING PARAMETERS OF
                  HAZARDOUS WASTE TRANSFER,  STORAGE,  AND
                      HANDLING OPERATION MODEL UNITS3
Model unit (weights,b %)
         Parameters
Container storage

   S01A   Drum storage (66.1)
   S01B   Drum storage (33.9)
   S01C   Dumpster storage (0)
Container loading

   Drum loading (NA)
   Drum loading (NA)
   Tank truck loading  (NA)
Throughput - 42 m3/yr
Volume - 0.21 m3/drum
Capacity - 100 drums
Turnovers - 2/yr
Spill fraction - 10-4
Volatilization fraction - 0.5

Throughput - 450 m3/yr
Volume - 0.21 m3/drum
Capacity - 180 drums
Turnovers - 12/yr
Spill fraction - 10~4
Volatilization fraction - 0.5

Throughput - 6.8 m3/yr
Windspeed - 4.5 m/s
Temperature - 25 °C
Length - 1.9 m
Width - 1.5 m
Height - 1.2 m
Turnovers - 2/yr
Throughput - 42 m3/yr
Volume - 0.21 m3/drum
Bulk temperature - 25 °C
Saturation factor
  (dimensionless) - 1.45
Number of loadings - 200/yr

Throughput - 460 m3/yr
Volume - 0.21 m3/drum
Bulk temperature - 25 °C
Saturation factor
  (dimensionless) - 1.45
Number of loadings - 2,200/yr

Throughput - 110 m3/yr
Volume - 27 m3
Bulk temperature - 25 °C
Saturation factor
  (dimensionless) - 1.45
Number of loadings - 4/yr
See notes at end of table.
                       (continued)
                                   C-41

-------
                TABLE C-4.   DESIGN  AND  OPERATING  PARAMETERS  OF
                    HAZARDOUS  WASTE TRANSFER,  STORAGE,  AND
                  HANDLING  OPERATION MODEL  UNITS9 (continued)
 Model  unit  (weights,b %)
          Parameters
 Container  loading  (con.)

    Tank truck  loading  (NA)
    Rail tank car loading (NA)
    Rail tank car loading (NA)
 Storage tanks

    S02A   Covered tank (37.7)
 Throughput - 430 m3/yr
 Volume - 27 m3
 Bulk temperature - 25 °C
 Saturation factor
  (dimensionless) - 1.45
 Number of loadings - 16/yr

 Throughput - 440 m3/yr
 Volume - 110 m3
 Bulk temperature - 25 °C
 Saturation factor
  (dimensionless) - 1.45
 Number of loadings - 4/yr

 Throughput - 1  800 m3/yr
 Volume - HO'm3
 Bulk temperature - 25 °C
 Saturation factor
  (dimensionless)  - 1.45
 Number of loadings - 16/yr
Throughput - 110 m3/yr  (30,000
  gal/yr)
Volume - 5.7 m3 (1,500  gal)
Diameter - 1.7 m (5.6 ft)
Adjustment for small diameter
 (dimensionless) - 0.26
Height - 2.4 m (8 ft)
Average vapor space height - 1.2 m
  (4 ft)
Average diurnal temperature
 change - 11 °C
Paint factor (dimensionless)
Turnovers - 20/yr
See notes at end of table.
                      (continued)
                                   C-42

-------
              TABLE C-4.  DESIGN AND OPERATING PARAMETERS OF
                  HAZARDOUS WASTE TRANSFER,  STORAGE, AND
                HANDLING OPERATION MODEL UNITS9 (continued)
Model unit (weights,b %)
         Parameters
Storage tanks (con.)

   S02B   Covered tank (Oc)
   S02C   Covered tank  (32.3)
   S02D   Covered tank  (17.8)
Throughput - 60 m3/yr (16,000
  gai/yr)
Volume - 30 m3 (8,000 gal)
Diameter - 4 m (13 ft)
Adjustment for small diameter
 (dimensionless) - 0.65
Height - 2.4 m (8 ft)
Average vapor space height - 1.2 m
  (4 ft)
Average diurnal temperature
 change - 11 °C
Paint factor (dimensionless) - 1
Turnovers - 2/yr

Throughput^- 1,100 m3/yr  (290,000
  gal/yr)
Volume - 30 m3  (8,000 gal)
Diameter - 4 m  (13 ft)
Adjustment for small diameter
 (dimensionless) - 0.65
Height - 2.4 m  (8 ft)
Average vapor space height - 1.2 m
  (4 ft)
Average diurnal temperature
 change - 11 °C
Paint factor  (dimensionless) - 1
Turnovers - 37/yr

Throughput - 3,300 m3/yr  (870,000
                                                       _
                                          Volume  -  76  m3  (20,000  gal)
                                          Diameter  - 5.8  m (19  ft)
                                          Adjustment for  small  diameter
                                           (dimensionless)  -  0.86
                                          Height  -  2.7 m  (9 ft)
                                          Average vapor space height - 1.4 m
                                            (4.6  ft)
                                          Average diurnal temperature
                                           change - 11 °C
                                          Paint  factor (dimensionless) - 1
                                          Turnovers -  44/yr
See  notes  at  end  of  table.
                       (continued)
                                    C-43

-------
                TABLE C-4.   DESIGN AND OPERATING PARAMETERS  OF
                    HAZARDOUS WASTE TRANSFER,  STORAGE,  AND
                  HANDLING  OPERATION MODEL UNITSa (continued)
  Model  unit  (weights,b  %)
                                         Parameters
  Storage tanks  (con.)

    S02E   Covered tank  (12.2)
                                Throughput - 17,000 m3/yr
                                  (4,500,000 gal/yr)
                                Volume - 800 m3 (210,000 gal)
                                Diameter - 9.1 m (30 ft)
                                Adjustment for small diameter
                                 (dimensionless) - 1
                                Height - 12 m (39 ft)
                                Average vapor space height -6m
                                  (20 ft)
                                Average diurnal  temperature
                                 change -  11 °C
                                Paint factor (dimensionless)
                                Turnovers  - 21/yr
 Treatment tanksd

    T01D   Covered quiescent tank (28.3)
   T01E
                                Throughput  -  11,000  Mg/yr
                                Volume  -  30 m3
                                Diameter  -4m
                                Adjustment  for  small diameter
                                 (dimensionless)  - 0.65
                                Height  -  2.4  m
                                Average vapor space  height - 1.2 m
                                Average diurnal temperature
                                change - 11  °C
                                Paint factor  (dimensionless) - 1
                                Retention time  - 24  h
                                Turnovers - 365/yr

Covered quiescent tank (21.8)   Throughput  -  28,000 Mg/yr
                                Volume - 76 m3
                                Diameter - 5.8 m
                               Adjustment for small  diameter
                                (dimensionless) - 0.86
                               Height - 2.7 m
                               Average vapor space height - 1.4 m
                               Average diurnal  temperature
                                change -  11 °C
                               Paint factor  (dimensionless)  -  1
                               Turnovers  -  365/yr
See notes at end of table.
                                                     (continued)
                                   C-44

-------
              TABLE C-4.  DESIGN AND OPERATING PARAMETERS OF
                  HAZARDOUS WASTE TRANSFER,  STORAGE,  AND
                HANDLING OPERATION MODEL UNITS9 (continued)
Model unit (weights,& %)
         Parameters
Treatment tanks (con.)

   T01F   Covered quiescent tank (50.0)  Throughput - 290,000 Mg/yr
                                         Volume - 800 ITH
                                         Diameter - 9.1 m
                                         Adjustment for small diameter
                                          (dimensionless) - 1
                                         Height - 12 m
                                         Average vapor space height - 6
                                         Average diurnal temperature
                                          change - 11 °C
                                         Paint factor (dimensionless)
                                         Turnovers - 365/yr
                               m
                             - 1
Equipment leaks

Equipment leak model unit Ae  (NA)
Pump seals - 5
Valves - 165
Sampling connections - 9
Open-ended lines - 44
Pressure relief valves - 3
NA = Not applicable.
Hazardous waste transfer, storage,  and handling operation model  units
  represent the  ranges of these  operations  in  the hazardous waste  management
  industry.
bBecause design characteristics and  operating parameters  (surface area,
  waste  throughputs, detention times,  and so on) were generally  not avail-
  able for all treatment, storage,  and disposal  facilities  (TSDF),  weighting
  factors were developed to approximate the nationwide  distribution of model
  units  defined  for a particular TSDF waste management  process.  The
  weighting factors are based on the  considerable statistical  data available
  in the 1981 EPA survey of hazardous waste generators  and  TSDF  conducted by
  Westat,  Inc.  (Westat Survey).   For  example,  results of this  survey were
  used to determine the national distribution  of sizes  of storage  tanks
  (storage volume), surface impoundments  (surface area),  and  landfills
  (surface area  and depth).   For further  information on weighting  factors,
  refer  to Appendix D, Sections  D.2.4.3 and D.2.5.
 cThe model unit was weighted 0% because  S02C  also  has  the same  volumetric
  capacity.   This avoids double-weighting of a unit size.
 dLoading emissions from covered quiescent  treatment tanks are estimated in
  the same manner as loading  emissions from covered storage tanks.
 eEquipment  leak model units  B  and C  were not  specified in terms of equip-
  ment counts.   Emission estimates and control costs were calculated on  the
  basis  of model unit  A equipment counts,  and  emission  and control costs
  for model units B and C  were  factored from  these  estimates.

                                    C-45

-------
  available to determine whether one loading  method  predominates.   This  load-
  ing  method creates  larger quantities  of  organic  vapors  and  increases the
  saturation factor of  each volatile compound within  the  container.  A satu-
  ration  factor is a  dimensionless  quantity that represents the expelled
  vapors  fractional approach to  saturation and accounts for the variations
  observed  in  emission  rates from the different unloading and  loading
  methods.59  /\ saturation  factor of 1.45 was  selected for the emission
  estimates, based on previous documentation  of splash-loading petroleum
  liquids.60,61  Typical capacities  for containers were selected, and 25 °C
  was considered the annual average  ambient operating temperature.
      Table C-4 presents covered, hazardous waste tank storage and quiescent
  treatment model units.  The tank sizes were  based on Westat Survey informa-
  tion, as has been explained previously for open hazardous waste quiescent
  treatment tank model units in Section C.2.1.1.  (The Westat Survey did not
  distinguish between  storage and treatment tanks.)  Turnovers per year were
 selected based on volumes of waste processed as reported in Westat62 anc|
 the Hazardous Waste  Data Management System.63  The remaining parameters
 were chosen,  based on  documented information and  engineering judgment,  to
 represent  hazardous  waste tank  storage processes.  Meteorological  condi-
 tions used represent standard temperature (25 °C)  and  daily average temper-
 ature change (11  °C).
      Table C-4 also  provides  hazardous waste transfer,  handling,  and  load-
 ing  (THL)  operation  model  units to estimate  emissions  from  equipment  leaks.
 The equipment leak model  unit A was obtained from the  benzene fugitives
 emissions  promulgation background  information document64 ancj was  usec|  as
 the baseline  to develop equipment  leak model  units  B and C.   Equipment  leak
 model units B and C were  not  specified  in terms of  equipment counts and,
 therefore,  are not presented  in  Table  C-4.   Emission estimates and control
 costs were  calculated  on  the  basis  of model  unit A  equipment  counts, and
 emissions and  control  costs for  model  units  B and C were factored  from
 these estimates.  Although the emission estimating model for  equipment
 leaks (essentially the  emission  factor) is independent of throughput, it
was necessary to account for throughput when  applying the model units to a
TSDF to estimate emissions.  TSDF may treat,   store, or dispose of  large
volumes of waste fay one management process.   Rather than assume that only
                                   C-46

-------
one very large process unit (and,  in turn,  one fugitive model  unit)  is
operated, the throughput of the process is  divided by the throughput of its
average model process unit, thus simulating the presence of multiple
process units.  This estimates the number of average model process units
operating at the TSDF, and one equipment leak model unit is then applied to
each average model process unit to estimate emissions from equipment leaks.
C.2.2  Model Wastes
     A set of model waste compositions was developed to provide a uniform
basis for emission control, emission reductions, and cost estimation for
the model waste management units.  Table C-5 lists the model waste
compositions.  These model wastes were used to develop control costs and
control  efficiencies by waste form for add-on and  suppression-type
controls.   It should be noted that the model waste compositions defined
here are not  used to estimate uncontrolled emissions from the  industry
facilities.   The compositions and quantities of actual waste streams
processed at  the existing  facilities were used to  estimate  nationwide  TSDF
emissions and the emission reductions  resulting from the  control  options.
     The waste stream  compositions  in  Table C-5 were selected  to  be repre-
sentative of  the major hazardous waste types containing  organics.66  One
EPA study using the  Waste  Environmental  Treatment  (WET)  data base67 cate-
gorized  organic-containing waste  streams into  major  classes and evaluated
pretreatment options for these  wastes.   That  study categorized organic-
containing  wastes  according  to  the  following  waste classes:68
      •    Organic  liquids
      •    Aqueous  organics (up  to 20 percent  organics)
      •    Dilute  aqueous  wastes (less than 2  percent organics)
      •    Organic sludges
      •    Aqueous/organic sludges.
      Other  data bases are available for specific industries,69 but compre-
 hensive waste stream listings for all domestic wastes are not available.
 Based on the known physical  and chemical forms of organic-containing
 wastes, the following six generic waste stream types were selected for
 evaluation  of add-on and suppression-type controls:
                                    O47

-------
i

• •
c ca

•S 15"
ll
I -
u

c.
o m
a. a.

is
s?
?° —
S «

4H
i •?

1 1

U J3
3 J*
S C
]i
— Cl
* ^5
§
u)

*
I
c M
o
*
T>
o


4?
C
1*
!*
5


Organic contant









*»>
•
^
*





ro
ca


^


S

CO

0
IJ
•







ff
Ok








•










•u
L.
"S
xS
58
ta 6









1
3
*
.3
^
0

ta
r«.
O)

r.
~



n



« A

•» u

at Cd
§f-
f*.









ci r-
e> 03
r» •«•







-* Q






O s



)'0X banzana
i0X naphtha lana
»9X phanol
16% banzana
IB% dlchlorobanzana
!EX naphtha lana
!5X haxachlorobanzana





j^
u
L.
3

•o a
1 1
— N

— —
c e
• •
o o




•"i
(O
M
t-*


^

«

N
!j
•
B







^
M






c
•
8?
0
C
M



Ul
CO



L0X dibutylphthalata
!.5X 1-haxanol
!.6X chloroform





X
I


1
•

o
3
?

m
ID
•r

10
~


a

«

10
a
•
Q















U
"c
s?
o
c
"



10



LX acatonltrila



•o

"o

CB
C
ntalnl
S
i
c
%
i
3
O
-z
m
H
m
e c
r_
II •
e u
o ~
1 »
o

S T
o — •
i !

= l
I ,
c o
o •»-
u

o e 4*

4» J^
8?S
•II
"out
o » a
• • o •
• o t, to
Tl C afl°
• 4> • U
o a c
• c-c a
il.-J
3 5— c
u u —
a x u
?i.l
a • 49 >
J=— • 0
4» a o L.
c? I a a
3 «5 •
|-c«
OT9 3-C
•>- • u
:.:?
t dafinad to provlda bai
ic charaical propartlaa
•oparttas of tha ramalnl
t- t— •— O>
a u
x •

««(/>(&
O— 1
3 3 «l'Q


o c a .a
Hi .2
o • »
•2 • • x
s * STJ
* -S— a
a j • a
Jr * u<
C-48

-------
     •     Dilute  aqueous  wastes
     •     Organic liquids
     •     Organic sludge/slurry
     •     Aqueous sludge/slurry
     •     Two-phase aqueous/organic
     •     Organic-containing solids.
     For each generic waste type,  specific chemical  compositions were next
defined so that material/energy  balances and costs could be calculated.
Chemical compositions were chosen  that represent the properties of hazard-
ous waste, but they may not represent specific constituents.  In general,
compositions were specified that are:
     •     Representative of the  generic waste stream type, i.e., that
          include the major organic chemical classes of environmental
          importance (e.g., chlorinated organics, aromatics)
     •     Composed of chemicals  representing a range of physical and
          chemical properties, based on Henry's law, biodegradability,
          and vapor pressure
     •     Physically and chemically realistic (e.g., a two-phase aque-
          ous/organic waste that in fact forms two phases at the pro-
          posed composition)
     •     Readily characterized by available physical and chemical
          property data  required for the treatment or control system
          process designs  (e.g., vapor-liquid equilibrium composi-
          tions) .
     To validate the criterion of being physically and chemically realis-
tic, small samples" of most of the selected generic waste  streams were
prepared.  However, the  physical and chemical properties  (e.g., vapor-
liquid equilibrium compositions) needed for the material  and energy
balances  have not been verified experimentally.  Many organic-containing
wastes  are complex multicomponent mixtures.  Trace  levels of certain
compounds (not examined  in this study)  could significantly  affect the
properties of a  particular waste stream.  However,  the chosen waste
compositions are generally suitable  for developing  design and  cost
information  for  treatment  and control  processes.
                                    C-49

-------
 C.2.3  Summary of Model Unit Analysis of Emission Reductions and Control
        Costs                                    ~~~—
      The model unit analysis was conducted to provide a basis for estimat-
 ing the effectiveness  (achievable emission reductions) and associated costs
 of controlling organic air emissions from TSDF hazardous waste management
 units.  In the model unit analysis, control costs (both capital and
 annualized) and achievable emission reductions were determined for a matrix
 of (1) TSDF model units (e.g.,  covered storage tanks, quiescent uncovered
 treatment tanks,  waste fixation operations, and open landfills), (2) waste
 forms (e.g., aqueous sludges, organic liquids, and dilute aqueous wastes),
 and (3)  control  technologies (e.g.,  suppression controls such as tank
 covers,  add-on controls such as carbon adsorbers).  The cost and emission
 reduction data generated in the analysis were then used to develop the
 control  technology and cost file used for estimating nationwide impacts for
 alternative TSDF  control  options.   This  fi'le provides control device
 efficiencies,  emission reductions,  and control costs according to waste
 form  for  each  emission control  technology that is applicable to a waste
 management  process.
      Table  C-6 presents a  summary  of the results, of  the model unit analysis
 in  terms  of uncontrolled emission  estimates,  emission reductions,  and
 control costs  for  the  various model  hazardous  waste  management  units.  This
 model unit  analysis  includes  only  compatible  combinations  of model  waste
 forms and model unit.   Incompatible  combinations  of  waste  form  and  model
 unit were not  analyzed; e.g., an organic-containing  solid  waste  would not
 be treated  in  a tank.
     In Table  C-6, the  emission control  refers to  the control technologies
 described in Chapter 4.0.  Model units and their  annual throughputs  are
 those described in Section C.2.1.  Model wastes are  as defined in Section
 C.2.2.  Uncontrolled emissions are estimates generated by  the applicable
 emission model described in Section C.I.I.  The emission reduction  is
calculated on the basis of efficiencies presented  in Chapter  4.0 for  each
control technology.  The costs of add-on and suppression-type controls are
calculated as described in Appendix H.
     The emission  estimates in Table C-6 show the wide range of emission
levels possible from a given model  waste management model unit when wastes
                                   C-50

-------
  TABLE  C-6.   SUMMARY  OF  TSDF  MODEL  UNIT  ANALYSIS  RESULTS'
b {
EMISSION !
CONTROL !
MODEL
WASTE TYPE
i
I ANNUAL
i TmOUGWUT
! (Mg/yr)
c,
UNCONTROLLED
EMISSIONS
(Mg/yr)
d
EMISSION
REDUCTION
(Mg/yr)
TOTAL !
CAPITAL i
INVESTMENT !
TOTAL
ANNUAL
COSTS
	 UUNtAlNCK SlUKflUL 	
— DRUM STORAGE (SOU) - 200 Dmms/yr — ,
Fixed Bed !
Carbon
Adsorber







Aqueous 50
Sludge
Dilute 40
Aqueous-1
Organic 40
Liquid
Organic 60
Sludge/Slurry
Two-Phase 40
Aqueous/Organic
0.00033 0.00031

0.0000083 0.0000079

0.0022 0.0021

0.0027 0.0026

0.000017 0.000016

$43,460 |

$43,460

$43,460

$43,460

$43,460

$18,300

$18,300

$18,300

$18,300

$18,300

— DRUM STORAGE (S01B) - 2200 Drums/yr —
Fixed Bed
Carbon
Adsorber







— DUMPSTER
Dumpster
Cover


! Aqueous 560'
0.0038 0.0034
Sludge j
Dilute 450
Aqueous-1
Organic 440
Liquid
Organic 610
Sludge/Slurry
Two-Phase 440
Aqueous/Organic
0.000091 0.000086

0.024 0.022
i
0.030 0.028

0.00018 0.00017
i i
$43,460 !

$43,460

$43,460

$43,460

$43,460

$18,300

$18,300

$18,300

$18,300

$18,300

STORAGE (S01C) - 3.4 m*3 (120 ftA3) Dumpster volume —
j Aqueous ' 16
i Sludge
! Organic 24
i .Solid
0.72 0-71

0.049 0.0485

$150

$150

$64

$72

See notes at end of table.
(continued)
                                C-51

-------
       TABLE  Cr6.   SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS'
b
EMISSION
CONTROL
MODEL
WASTE TYPE
ANNUAL
THROUGHPUT
(Mg/yr)
! c|
! UNCONTROLLED |
! EMISSIONS !
i (Mg/yr) j
d
EMISSION
REDUCTION
(Mg/yr)
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
— COVERED
Internal
Floating
Roof




Vent to
Existing
Control
Device



Vent to
Carbon
Canisters




STORAGE TANK (S02A) -
Aqueous
Sludge

Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge

Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
\queous/0rganlc
».uiji..ii^.n^.K-»ju»gass»3£=s3ai
• i/um
1,500 gal
140

110
110
130
131
i
140
110
110
130
131
140

110
110
130
131
^g-»^-»— • — 1--T.
OIUttAUL 	
tank —
0.0045

0.083
0.017 .
0.043
0.035
0.0045
0.083
0.017
0.043
0.035
0.0045

0.083
0.017
0.043
0.035

0.004

0.061
0.014
0.035
0.027
• 0.004
0.079
0.016
0.041
0.033
0.004

0.079
0.016
0.041
0.033

$4,820

$4,820
$4,820
$4,820
$4,820
$1,600
$1,600
$1.600
$1,600
$1,600
$1,050

$1,050
$1,050
$1,050
$1,050

$1 ,520

$1,520
$1,520
$1,520
$1,520
$320
$320
$320
$320
$320
$2,220

$5,330
$2,800
$3,520
$3,500
See notes at end of table.
(continued)
                                 C-52

-------
      TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS'
b
EMISSION
CONTROL
MODEL ANNUAL
WASTE TYPE THROUGHPUT
(Mg/yr)
cj d
UNCONTROLLED EMISSION TOTAL TOTAL
EMISSIONS REDUCTION CAPITAL ANNUAL
(Mg/yr) (Mg/yr) INVESTMENT COSTS
	 TAUI/ crnonnp 	 	
— COVERED STORAGE TANK (S02B) -
Internal
Floating
Roof



Vent to
Existing
Control
Device



Vent to
Carbon
Canisters



Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous !
Sludge |
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
8,000 gal tank —
70
60
60
70
70
70
60
60
70
70
70
60
60
70
70
0.013
0.180
0.0465
0.114
0.075
0.013
0.180J
0.0465
0.114
0.075
0.013
0.180
0.0465
0.114
0.075
0.011
0.133
0.038
0.093
0.058
0.012
0.171
0.044
0.108
0.071
0.012
0.171
•0.044
0.108
0.071
$8,400
$8,400
$8,400
$8,400
$8,400
$1,600
$1,680
$1,600
$1,600
$1,600
$1,050
$1,050
$1,050
$1,050
$1,050
$2,600
$2,600
$2,600
$2,600
$2,600
$320
$320
$320
$32o
$320
$2,220
$8,720
$3,520
$6,100
$4,810
See notes at end of table.
(continued)
                                  C-53

-------
        TABLE C-6.   SUMMARY OF TSDF MODEL UNIT ANALYSIS'.RESULTS6
b
EMISSION
CONTROL

— COVERED
Internal
Floating
Roof



Vent to
Existing
Control
Device



Vent to
Carbon
Canisters



j _ 	 	
MODEL
HASTE TYPE
i

STORAGE TANK (S02
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
! Aqueous
Sludge
! Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic!
.
ANNUAL
TfflOUGHPUT
(Mg/yr)
TANK
C) - 8,000 gal
1,380
1,120
1,090
1,320
1,300
i
1,380
•1,120
1,090
1.320
1,300
1,380
1,120
1,090
1,320
1,300
UNCONTROLLED
EMISSIONS
(Mg/yr)
:CTnDAPC
tank —
0.045
0.813
0.167
0.424
0.342
0.045
0.813
0.167
0.424
0.342
0.045
0.813
0.167
0.424
0.342
i
m t 	 =AU!iMJJt=s
EMISSION
REDUCTION
(Mg/yr) \


0.037
0.602
0.137
0.348
0.267
0.043
0.772
0.159
0.403
0.325
0.043
0.772
0.159
0.403
0.325
TOTAL
CAPITAL
INVESTMENT


$8,400
$8,400
$8,400
$8,400
$8,400
$1,600
$1,600-
$1,600
$1,600
$1,600
$1,050
$1,050
$1,050
$1,050
$1,050
TOTAL
ANNUAL
COSTS


$2,600
$2,600
$2,600
$2,600
$2,600
$320 '
$320
$320
$320
$320
$3,530
$34,130
$8,730
$18,500
$15,220
See notes at end of table.
(continued)
                                   C-54

-------
      TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS*
b
EMISSION
CONTROL

— COVERED
Internal
Floating
Roof



Vent to
Existing
Control
Device



Vent to
Carbon
Canisters



MODEL ANNUAL
WASTE TYPE THROUGHPUT
! (Mg/yr)
	 	 TAI,
STORAGE TANK (S02D) - 20,000 J
Aqueous 4,100
Sludge
Dilute 3,300
Aqueous-1
Organic 3,200
Liquid
Organic 3,900
Sludge/S lurry
Two-Phase 3,900
Aqueous/Organic
Aqueous 4,100
Sludge
Dilute 3,300
Aqueous-1
Organic 3,200
Liquid
Organic 3,900
Sludge/Slurry
Two-Phase 3,900
Aqueous/Organic
Aqueous 4,100
Sludge
Dilute 3,300
Aqueous-1
Organic 3,200
Liquid
Organic 3,900
Sludge/Slurry
Two-Phase 3,900
Aqueous/Organic
c
UNCONTROLLED
EMISSIONS
(Wg/yr)
IK STORAGE 	
jal tank —
0.117
2.12
0.437
1.11
0.891
0.117
2.12
0.437
1.11
0.891
0.117
2.12
0.437
1.11
0.891
d
EMISSION
REDUCTION
(Mg/yr)


0.096
1.569
0.358
0.910
0.695
0.111
2.014
0.415
1.055
0.846
0.111
2.014
0.415
1.055
0.846
TOTAL
CAPITAL
INVESTMENT


$11,380
$11,380
$11,380
$11,380
$11,380
.
$1,600
$1,600
$1,600
$i,600
$1,600
$1,050
$1.050
$1,050
$1,050
$1,050
TOTAL
ANNUAL
COSTS


$3,500
$3,500
$3,500
$3,500
$3,500
$320
$320
$320
$320
$320
$8,110
$87,600
$20,480
$47,240
$38,750
See notes at end of table,,
(continued)
                                   C-55

-------
       TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS3
b !
EMISSION |
CONTROL j
i
MODEL
WASTE TYPE
i
ANNUAL !
THROUGHPUT i
(Mg/yr) 5
c!
UNCONTROLLED J
EMISSIONS i
(Mg/yr) j
d
EMISSION
REDUCTION
(Mg/yr)
"
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
	 \nn\ OIUHAUC 	
— COVERED STORAGE TANK (S02E) - 210,000 gal tank 	
Internal
Floating
Roof



Vent to
Existing
Control
Device


Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phasa
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Vent to
Fixed Bed
Carbon
Adsorber


Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
20,520
16,660
16,260
19,640
19,300
20,520
16,660 J
16,260
19,640
19,300
20,520
16,660
16,260
19,640
19,300
0.678
12.35
2.53
6.43
5.19
0.678
12.35
2.53
6.43
5.19
0.678
12.35
2.53
6.43
5.19
0.556
9.139
2.075
5.273
4.048
0.644
11.733 .
2.403
6.108
4.931
0.644
11.733
2.403
6.108
4.931
$19,660
$19,660
$19,660
$19,660
$19,660
$1,600
$1,600
$1,600
$1,600
$1,600
$72,300
$72,300
$72.300
$72,300
$72,300
$6,100
$6,100
$6,100
$6,100
$6,100
$11,080
$15,660
$13,170
$13,160
$13,700
$40,000
$50,480
$40,000
$40,260
$40,140
"See notes at end of table.
                                                           (continued)
                                   C-56

-------
 TABLE  C-6.   SUMMARY OF TSDF  MODEL  UNIT ANALYSIS  RESULTS'
  EMISSION
  CONTROL
  MODEL
WASTE TYPE
  ANNUAL
TtfiOUGHW
 (Mg/yr)
UNCONTROLLED
 EMISSIONS
  (Mg/yr)
EMISSION
REDUCTION
 TOTAL
CAPITAL
                                               (Mg/yr)   i INVESTMENT
TOTAL
ANNUAL
COSTS
                               TANK STORAGE
— QUIESCENT UNCOVERED STORAGE TANK (S02F) - 1.500 gal tank —
Fixed Roof !




Internal
Floating
Roof
( + fixed
roof)



Vent to
Existing
Control
Device
( + fixed
roof)


Vent to
Carbon
Canister
( + fixed
roof)



Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
140
110
110
130
130
140
110
110
130
130
140
110
110
130
130
140
110
110
130
13C
1.5
0.38
26
31
0.39
1.5
0.38
26
31
0.39
1.5
_
0.3S
26
31
0.33
1.5
0.36
26
31
0.39
1.496
0.28
25.98
30.96
0.36
1.499
0.34
. 25.996
30.99
0.383
1.4998
0.356
25.999
30.998
0.389
1.4998.
• 0.356
25.939
30.998
0.389
:
$3,790
$3.790
$3.790
$3,790
$3.790
$7.330
$7,330
$7,330
$7.330
"
$7.330
$5,370
$5,370
$5,370
$5,370
$5,370
$4,840
$4,840
$4,840
$4,840
$4,840
$760
$760
$760
$760
$760
$1,870
$1,870
. $1,870
$1,870
$1,870
$1,080
$1.080
$1,080
$1,080
$1,080
$2.980
$6.090
$3,560
$4.280
$4.260
 See notes  at  end of table.
                                                  (continued)
                                 C-57

-------
  TABLE C-6.   SUMMARY  OF TSDF MODEL  UNIT ANALYSIS RESULTS'
EMISSION
CONTROL
               MODEL
             WASTE TYPE
  ANNUAL   ! UNCONTROLLED ! EMISSION  |    TOTAL
THROUGHPUT !  EMISSIONS   i REDUCTION  !   CAPITAL
 (Mg/yr)   !   (Mg/yr)    i  (Mg/yr)  !  INVESTMENT
TOTAL
ANNUAL
COSTS
                                TANK
 — QUIESCENT UNCOVERED STORAGE TANK (S02G) - 8.000 gal tank —
Fixed Roof







Internal
Floating
Roof
( + fixed
roof)



Vent to
Existing
Control .
Device
(•i- fixed
roof) •




Vent to
Carbon
Canister
( + fixed
roof)




! Aqueous ! 70
j Sludge j
Dilute j 60
Aqueous-1 j
Organic j 60
Liquid i
Organic i 70
Sludge/Slurry !
1 '
Trio-Phase i 70
Aqueous/Organic!
Aqueous ! 70
Sludge !
1
Dl lute j 60
Aqueous-l !
Organic I 60
• Liquid j
Organic ! 70
Sludge/Slurry j
Trio-Phase i 70
Aqueous/Organic!
Aqueous ! 70
Sludge j
1
Dl lute ! 60
Aqueous-1 j
j
Organic | 60
Liquid j
i
Organic I 70
Sludge/Slurry !
Trio-Phase ! 70
Aqueous/Organic!
Aqueous ! 70
Sludge ;
-3 1

Dilute I 60
Aqueous-1 |
Organic i 60
Liquid !
i
Organic ! 70
Sludge/Slurry !
Tho-Phase i 70
queous/Orcanlc!
! 1.4
t
0.24

24
29

0.23
1.4

0.24
24
29
0.23
1.4
0.24

24

29
0.23
1.4

0.24
24

29
0.23
! 1.39
i
0.06

23.95
28.89

0.16
1.398

0.19
23.99
28.98
0.21
1.3995
0.23

23.998

28.99
0.227
1.3995

0.23
23.998

28.99
0.227
$9,500

$9,500

$9,500
$9.500

$9,500
$16,450

$16,450
$16,450
$16,450
$16,450
$11,080
$11,080

$11,030

$11,030
$11,030
$10.550

$10,550
$10,550

$10,550
$10,550
$1,880

$1,880

$1,880
$1.880

$1.830
$4.000

$4,000
$4,000
$4.000
t
,
$4.000
$2,200
$2,200

$2,200

$2,200
$2,200
$4,100

S10.600
$5,4GO

$7,9SO
$6,690
See notes at end of table.
                                                           (continued)
                                C-58

-------
TABLE C-6.   SUMMARY OF TSDF MODEL  UNIT ANALYSIS  RESULTS0
b
EMISSION
CONTROL
MODEL
KASTE TYPE
ANNUAL
THROUGHPUT
(Mg/yr)
c
UNCONTROLLED
EMISSIONS
(Mg/yr)
d
EMISSION
REDUCTION
(Mg/yr)
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
                         TANK STORAGE
  QUIESCENT UNCOVERED STORAGE TANK (SQ2H) - 8.000 gal tank —
Fixed Roof









Internal
Floating
Roof
( + fixed
roof)



•


Vent to
Existing
Control
Device
( + fixed
roof)





Vent to
Carbon
Canister
{ + fixed
roof)






Aqueous
Sludge
Dilute
Aqusous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge

Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge

Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Tvio-Ttese
Aqueous/Organ)
1,380

1.120

1,090

1.320

1,300

1,380


1.120

1.090

1.320

1,300

1,380
.
i
; 1,120

1.090

1,320

1,300

1,330


1,120

1,030

1,320

1,300

11

3.2

217

243

3.6

11


3.2

217

243
1
3.6

11

3.2

217

243

3.6

11


3.2

217

243

3.6
!
10.96

2.4

216.8

242.6

3.3

10.99


3.0

216.98

242.9

3.53

10.998

I
3.16

216.99

242.98

3.59

10.998


3.16

216.99

242.93

3.59

$9,500

$9,500

$9.500

$9.500

$9.500

$16,450


$16,450

$16,450

$16,450

$16,450

$11,080

$11,080

$11.080

$1 1,030

$11,080

$10,550


$10.550

$10,550

$10,550

J10.550

$1,880

$1,880

$1.880

$1,880

$1,880

$4,000


$4,000

$4,000

$4.000

$4,000

$2.200

$2,200

$2,200

$2,200

$2,200

$5,410


$33,010

$10.610

S20.330

$17,100

 See notes at  end of table.
(continued)
                           C-59

-------
    TABLE  C-6.   SUMMARY  OF TSDF  MODEL  UNIT ANALYSIS  RESULTS9
    EMISSION
                 MODEL
    tmiooiun  j     MUUCL
    CONTROL  j  WASTE TYPE
  ANNUAL   i UNCONTROLLED
TffiOUGHPUT !  EMISSIONS
 (Mg/yr)   !   (Mg/yr)
EMISSION   i    TOTAL    !   TOTAL
REDUCTION     CAPITAL      ANNUAL
 (Mg/yr)   \ INVESTMENT  !   COSTS
                                - TANK STORAGE
  — QUIESCENT UNCOVERED STORAGE TANK (S02I) - 20.000 flal —
Fixed Roof






Internal
Floating
Roof
( + fixed
roof)





Vent to
Existing
Control
Device
( + fixed
roof)




Vent to
Carbon
Canister
( + f Ixsd
roof)




! Aqueous
Sludge
Dilute
Aqueous-1

Organic
Liquid

Organic
Sludge/Slurry
Two-Phase
Aqueous/Organ
Aqueous
Sludge

Dilute
Aqueous-1

Organic
Liquid

Organic
Sludge/Slurry
Two-Phase
Aqueous/Organl
Aqueous
Sludge
Dilute
Aqueous-1

Organic
Liquid
Organic
Sludge/Slurry

Two-Phase
queous/Organlc
Aqueous
Sludge
Dilute
Aqueaus-1
Oraanic
Liquid
Organic
ludgs/Slurry

Two-Phase
queous/Organlc
4.100 |
1
1
3,300 J
i
i
3.200 j
I

3.900 j
I
1
3.900 j
i
4.100 !

3,300 j
i
3,200 !
t
i
3,900 !
i
i ,
t
3,900 !
4,100 !
j
3,300 j
t
3.200 i
1
3,900 j

3,900 !
i
i
4,100 !
1
t
1
3,300 i
t
t
3.200 i
I
1
3,900 j
i
t
3.900 i
i
1'
8.1

514

586
9.7
24

8.T

514

586
9.7
24
8.1

514
586

9.7
24
8.1
514
5£3

9.7
23.9 !
i
i
6.0 j
i
j
513.6 j

1
584.9 1
8.8 j
23.98 j
1
I
7.6 j

. 513..9 j
1
585.8 !
1
9.5 j
23.995 j
<
I .
8.0 j
j
513.98 !
i
585.9 !

9.66 j
1
1
23.995 !
1
J
1
8.0 !
1
513.98 !
i
i
5S5.9 !
1
1
t
9.66 I
1
$14.800 j
$14,800 j
j
1
$14,800 j
i
i
$14,800 j
j
$14,800 j
1
$24,420 1
t
i
$24,420 j
1
I
$24,420 !
1
t
$24.420 i
I
1
$24,420 !
i
$16,380 !
1
1
1
$16,380 >
j
$16.380 i
t
I
$16,380 i
I
1
$16,380 i
1
1
$15.850 |
I
I
$15,850 j
$15,850 !
1
1
515.850 i

1
$15,850 i
$2,930
$2,930

$2.930

$2.930
$2,930
$5,860

$5,860

$5,860

$5,860
$5,860
$3,250
$3,250

$3,250
$3.250

$3,250
$11,040
$90,530
$23,410
$50,170

$41.650
See notes at end of table.
                                   (continued)
                              C-60

-------
TABLE C-6.   SUMMARY  OF TSDF MODEL  UNIT ANALYSIS  RESULTS'
b
EMISSION
CONTROL
MODEL
WASTE TYPE
ANNUAL
THROUGHPUT
(Mg/yr)
0
UNCONTROLLED
EMISSIONS
(Mg/yr)
o :
EMISSION !
REDUCTION |
(Mg/yr) !
•TOTAL
CAPITAL
INVESTMENT
1
i TOTAL
! ANNUAL
! COSTS
                          TANK STORAGE
  QUIESCENT UNCOVERED STORAGE TANK (S02J) - 210.000 gal tank
rlxed Roof









Internal
Floating
Roof
( + fixed
roof)






Vent to
Existing
Control
Device
( + fixed
roof)





Vent to
Fixed Bed
Carbon
Adsorber
( t fixed
roof)





Aqueous
Sludge
Dilute
Aqueous-1
Organic I
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two -Phase
Aqueous/Organ 1
20.520

16,660

16,260

19,640

19,300

20,520

16,660

16,260

19,640

19,300

20.520

16,660

16,260

19,640

19,300

20,520

16,660

16,260

19,640

13.300

70

30

1,730

1,960

41

70

30

1,730

1.960

41

70

30

1,730

1.960

41

70

30

1,730

1,960

41

69.3 j

17.7

1,727

1,954

35.8

69.9

26.8

1,729.5

t.958.9

39.9

69.97

29.4

1,729.9

1959.7

40.7

6S.97
'
29.4

1,729.9

1959.7

40.7

$26.040

$26,040

$26,040

$26,040

$26,040

$40,560

$40,560

$40.560

$40,560

$40,560

$27,620

$27,620

$27,620

$27,620

$27,620

$98,340

$98,340

$98,340

$98,340

$98,340

$5.200

$5,200

$5.200

$5.200

$5,200

$9,500

$9,500

$9,500

$9,5pO

$9,500

$5,600
;
$5,600'

$5,600

$5,600

$5,600

$45,200

$55,6SQ

$45,200

$45,400

$45,340

 See notes  at end  of table.
(continued)
                             C-61

-------
     TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS'
b
EMISSION
CONTROL

!
| MODEL
! HASTE TYPE
!

ANNUAL
THMHJGHW
(Mg/yr)
c
UNCONTROLLED
EMISSIONS
(Mg/yr)
d
EMISSION
REDUCTION
(Mg/yr)

TOTAL
CAPITAL
INVESTMENT
"== — ="• —
TOTAL
ANNUAL
COSTS
— — — IIHOIU ILL OIUftMUL 	
— WASTEPILE COVER (S030) - 1300 ftA3 waste volume —
Hasteplle j Aqueous J 17,000 J 16.0 15.95 !
Cover-30 nil Sludge ! j
HOPE j !
Two-Phase ! 17,000 10.0 4.9 1
iAquaous/Organlcj | j
— HASTEPILE COVER (S03E) -
Wasteplle Aqueous
Cover-30 nl 1 Sludge
HOPE
Two-Phase
Aqueous/Organic
— HASTEPILE COVER (S03F) -
Wasteplle Aqueous
Cover-30 all Sludge
HOPE
Two-Phase
Aqueous/Organic
16,000 ftA3 waste volume —
120,000 139.7 139.3 S
120,000 100.0 49.3 $
I
2,010,000 ftA3 waste volume —
170,000 457.0 j 455.6 $1£
i
170,000 390.0 192.3 $1£
i
i
$650 $2,500
t
t
$650 $2,500
6,480 $4,700
6,480 $4,700
i
7,300 $62,000
7,300 $62,000
See notes at end of table.
(continued)
                                C-62

-------
    TABLE C-6,   SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS'
b
EMISSION
CONTROL


MODEL ANNUAL
WASTE TYPE THROUGHPUT
(Mg/yr)
OIIO
— QUIESCENT STORAGE IMPOUNDMENT (S04A) -
ASP+FBCA
Aqueous 99,000
c!
UNCONTROLLED
EMISSIONS
(Mg/yr)
PAPF IlPmiNHMFMT
d
EMISSION
REDUCTION
(Mg/yr)
crrnACF
i
TOTAL
CAPITAL
INVESTMENT


TOTAL
ANNUAL
COSTS

71 ,300 gal Impoundment —
278
264
i Sludge





Dilute 99,000
Aqueous-1

Two-Phase 99,000

MEMBRANE





Aqueous/Organic
Aqueous 99,000
Sludge
Dilute 99,000
Aqueous-1
Two-Phase 99,000
Aqueous/Organic
— QUIESCENT STORAGE IMPOUNDMENT (S04B) -
ASP-:FBCA





MEMBRANE





Aqueous 9,800
Sludge
Dilute 9,800
Aqueous-1
Two-Phase 9,800
Aqueous/Organic
Aqueous 9,800
Sludge
Dilute 9,800
Aqueous-1
Two-Phase 9,800
Aqueous/Organic

114


191
,-
278

114

" 191


108


181

236

97

162

$181 ,000


$177,000


$177,000
1
$15,000

$15,000

$15,000
i
$84,000


$78,000


$78,000

$8,000

$8,000

$8,000

• 71,300 gal Impoundment —
140

32

i 36

140

32

36

133

30

34

119

27

31

$180,000

! $179,000

! $179,000
1
$15,000

$15,000

$15,000

$78,000

$74,000

$74,000

$8,000

$8,000

$8,000

See notes at end of table.
(continued)
                                 C-63

-------
TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS'
b
EMISSION MODEL ANNUAL
CONTROL WASTE TYPE THROUGHPUT
(Mg/yr)
c d
UNCONTROLLED EMISSION TOTAL
EMISSIONS REDUCTION CAPITAL
(Mg/yr) (Mg/yr) INVESTMENT
TOTAL
ANNUAL
COSTS
	 	 SURFACE IMPOUNUffMT STORAGE 	 	
— QUIESCENT .STORAGE UPOUNDMENT (S04C) - 713,000 gal impoundment —
ASP+FBCA Aqueous 49,000
Sludge
Dilute 49,000
Aqueous-1
Two-Phase 49,000
i Aqueous/Organic
MEMBRANE Aqueous 49,000
Sludge
Dilute 49.000
Aqueous-1
Two-Phase 49,000
Aqueous/Organic
— QUIESCENT STORAGE IMPOUNDMENT (S04D) -
ASP+FBCA i Aqueous 25,000
Sludge
Dl lute 25,000
! Aqueous-1
Two-Phase 25,000
Aqueous/Organic
MEMBRANE Aqueous 25,000
Sludge
Dilute 25,000
Aqueous-1
Two-Phase 25,000
Aqueous/Organic
See notes at end of table.
^^^_^_^^__^_^^_!__
686 652 $311,000
1
1
159 j 151 $249,000
183 174 $249,000
i
686 583 $57,000
159 135 ' $57,000
183 156 $57,000
' ' .
• 713,000 gal Impoundment —
442 420 $310,000
i
157 149 $310,000
S3 88 $310,000
442 376 $57,000
157 133 $57,000
93 79 $57,000
i
$42,000
$42,000
$42,000
$16,200
$16,200
$16,200

$127,000
$114,000
$114,000
$17,000
$17,000
$17,000
(continued)
C-64
.

-------
     TABLE C-6.   SUMMARY OF TSDF MODEL  UNIT  ANALYSIS  RESULTS0
b
EMISSION
CONTROL
MODEL ANNUAL
HASTE TYPE THROUGtfW
(Mg/yr)
c d
UNCONTROLLED EMISSION
EMISSIONS REDUCTION
(Mg/yr) (Mg/yr)
i
TOTAL
CAPITAL
i INVESTMENT
TOTAL
ANNUAL
COSTS
	 cjiOFAPF IMPnUNDUFNT STORAGE 	 	
— QUIESCENT STORAGE IMPOUNDMENT (S04E) - 8,720,000 gal Impoundment —
ASP+FBCA

Aqueous 120,000
Sludge
Di lute 120,000
Aqueous-1
Two-Phase 120,000
{Aqueous/Organic


MEMBRANE Aqueous 120,000
Sludge
! Dilute 120,000
Aqueous-1

Two-Phase 120.000
Aqueous/Organic
— QUIESCENT STORAGE IMPOUNDMENT (S04F) -
ASP+FBCA


MEMBRANE


Aqueous 67,000
Sludge
DI lute 67,000
Aqueous-1
Two-Phase 67,000
Aqueous/Organic
i
Aqueous 67,000
Sludge
Di lute 67,000
Aqueous-1
Two-Phase 67,000
Aqueous/Organic
2,200 2,090
446 424
464 441

2,200 1,870
446 379
464 394
8,720,000 gal Impoundment
1,420 1.3«3
253 240
i
i
262 249
i
1,420 1,207
253 215
•
262 223
$1,160,000
$804,000
$804,000
i
$300,000
$300,000
$300,000
1
vi—
j $1,170,000
$806,000
$806,000
i
$300,000
$300,000
$300,000
$488,000
$284,000
$284,000

$65,000
$65,000
$65,000

$450,000
$276,000
$276,000
$65,000
$65,000
$65,000
See notes at end of table.
(continued)
                                 C-65

-------
       TABLE  C-6.  SUMMARY OF TSDF MODEL  UNIT ANALYSIS RESULTS*
b
EMISSION
CONTROL
MODEL
HASTE TYPE
ANNUAL
THROUGHPUT
(Hg/yr)
p
UNCONTROLLED
EMISSIONS
(Mg/yr)
d
EMISSION
REDUCTION
(Mg/yr)
TOTAL
CAPITAL
INVESTMENT
=3Sa=3S=SSr==
TOTAL
ANNUAL
COSTS
                         	 TANK TREATMENT -
 — QUIESCENT UNCOVERED TREATMENT TANK (T01A) - 8,000 gal
tank
Fixed Roof





Internal
Floating
Roof
( + fixed
roof)


Vent to
Existing
Control
Device
( + fixed
roof)


Vent to
Carbon
Canister
( + fixed
roof)


Aq Sludge
Dilute Aq
Org Liquid
Org Sludge/Slurry
THO-Phasa Aq/Org

Aq Sludge
Dilute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge
Dilute Aq
Org Liquid
C/g Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge
Dl lute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
11,000
11,000
11,000
11,000
' 11,000

11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
16
8.6
467
523
14

16
8.6
467
523
14
16
8.6
467
523
14
16
8.6
467
523
14
15.9 j $9,500
6.8 j $9,500
466.5 | $9,500
522.4 j $9,500
13.2 j $9,500
i
15.98 j $16,450
8.12 j $16,450
466.91 j $16,450
522.90 | $16,450
13.83 i $16,450
15.995 ! $11,080
[
8.51 j $11,080
466.98 j $11,080
522.97 j $11,080
13.96 i $11,080
15.995 j $10,550
8.5 j $10,550
466.98 j $10,550
522.97 j $10,550
13.96 {' $10,550
$1,880
$1,880
$1,880
$1,880
$1,880

$4,090
$4,090
$4,090
$4,090
$4,090
; $2,210
$2,210
$2,210
$2,210
$2,210
$7,300
$76,380
$22,360
$25)570
$34,090
See notes at end of table.
                  (continued)
                                     C-66

-------
     TABLE  C-6.   SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS
b
EMISSION
CONTROL

!
MODEL ! ANNUAL
WASTE TYPE ! THROUGHPUT
! (Mg/yr)
c
UNCONTROLLED
EMISSIONS
(Mg/yr)
d
EMISSION
REDUCTION
(Mg/yr)

TOTAL
CAPITAL
INVESTMENT

TOTAL
ANNUAL
COSTS
————— IHTIIV intMimtm — — — — —
— QUIESCENT UNCOVERED TREATMENT TANK (T01B) - 20,000 gal tank —
Fixed Roof




Internal
Floating
Roof
( + fixed
roof)


Vent to
Existing
Control
Device
( + fixed
roof)

Vent to
Carbon
Canister
( + fixed
roof)


Aq Sludge
Dilute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge
Dl lute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge
i
Dl lute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge
Dilute Aq
Org Liquid
Org Sludge/Slurry
! Two-Phase Aq/Org
28,000
28,000
28,000
28,000
28,000
28,000
28,000
28,000
28,000
28,000
28,000
28.000
28,000
28,000
28,000
28,000
28,000
28,000
23,000
28,000
34
19
954
1,026
31
34
19
954
1,026
31
34
1
19
954
1,026
31
34
19
954
1,026
31
33.8
14.4
952.8
1,024.6
29.1
33.96
17.80
953.79
1025.75
30.57
33.99
18.8
953.9
1025.9
30.9
33.99
18.8
953.9
1025.9
30.9
$14,800
$14,800
$14,800
$14,800
$14,800
$24,420
$24,420
$24,420
$24,420
$24,420
$16,380
$16,380
$16,380
$16,380
$16,380
$15,850
$15,850
$15,850
$15,850
$15,850
$3,050
$3,050
$3,050
$3,050
$3,050
$6,100
$6,100
$6,100
$6,100
$6,100
$3,350
$3,350
$3,350
$3,350
$3,350
$15,790
$188,920
$53,460
$20,220
$82,830
See notes at end of table.
(continued)
                                 C-67

-------
      TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS'
b
EMISSION
CONTROL
MODEL
WASTE TYPE
i ANNUAL
! THROUGHPUT
! (Mg/yr)
c
UNCONTROLLED
EMISSIONS
(Mg/yr)
d
EMISSION
REDUCTION
(Mg/yr)
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
— ^— — — - i«™\ intHimcm — — — —
— QUIESCENT UNCOVERED TREATMENT TANK (T01C) - 210,000 gal tank —
Fixed Roof




Internal
Floating
Roof
(• £. \\*ftf&
+ f Ixsd
roof)
.

Vent to
Existing
Control
Device
( + fixed
*>jti*£\
roof)


Vent to
Fixed Bed
Carbon
Adsorber
( + fixed
ff\ft£.\
roof)


Aq Sludge
DI lute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Drg
Aq Sludge
Dilute Aq

Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge
DI lute Aq
Org Liquid

Org Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge
DI lute Aq
Org Liquid

Org Sludge/Slurry
Two-Phase Aq/Org
290,000
290,000
290,000
290,000
290,000
290,000
290,000

290,000
290,000
290,000
290.000
290,000
290,000

290,000
290,000
290,000
290,000
290,000

290,000
290,000
83
53
4,770
5,320
98
83
53

4,770
5,320
98
83
53
4,770

5,320
98
83
53
4,770

5,320
98
80.6
5.8
4,759
5,306
78.1
68.06
60.16

3912.44
5219.01
1243.69
82.88
50.64
4769.45

5319.28
97.01
$26,040
$26,040
$26,040
$26,040
$26,040
$40,560
$40.560

$40,560
$40,560
$40,560
$42,460
$42,460
$42.460

$42.460
$42.460
82.88 $100,220
50.64 $100,220
4769.45 $100,220

5319.28 $100,220
97.01 $100,220
$5.810
$5,810
$5,810
$5,810
$5.810
$11,620
$11,620

$11,620
$11,620
$11,620
$8',720
$8,720
$8,720

$8,720
$8,720
$58,120
$58,120
$58,120

$58,120
$58, 120
See notes at end of table.
(continued)
                                C-68

-------
     TABLE C-6o   SUMMARY OF TSDF  MODEL UNIT ANALYSIS RESULTS'
b
EMISSION
CONTROL
MODEL
HASTE TYPE
! ANNUM.
j THROUGWtJT
! (Mg/yr)
! c
i UNCONTROLLED
i EMISSIONS
! (Mg/yr)
d!
EMISSION !
REDUCTION i
(Mg/yr) i
TOTAL
CAPITAL
INVESTMENT
                                                                   TOTAL
                                                                   ANNUAL
                                                                   COSTS
                              TANK TREATMENT
— COVERED C
Internal
Floating
Roof



Vent to
Existing
Control
Device

Vent to
Carbon
Canister



IUIESCENT TREATMENT
Aq Sludge
Dl lute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge
Dl lute Aq
Org Liquid
Org Sludge/Slurry
i Two-Phase Aq/Org
Aq Sludge
Dl lute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
TANK (T01D)
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11,000
11.000
11,000
11,000
i 11,000
- 8,000 gal tar
0.0953
1.83
0.473
0.56
0.769
0.0953
1.83
0.473
0.58
0.769
0.0953
1.83
0.473
0.56
0.769
k —
0.08
1.35
0.39
0.46
0.60
0.09
1.74
0.45
0.53
0.73
0.09.
»
1.74'
0.45
0.53
0.73

$8,400
$8,400
$8,400
$8,400
$8,400
$1,600
$1,600
$1,600
$1,600
$1,600
$1,050
$1,050
$1,050
$1,050
$4,900

$2,660
$2,660
$2,680
$2,660
$2,660
$330
$330
$330
$330
$330
$5,420
1
$74,500
$20,480
$23,690
$32,210
See notes  at end of table.
(continued)
                                    C-69

-------
        TABLE C-6.   SUMMARY OF TSDF MODEL  UNIT ANALYSIS RESULTS3
b i
EMISSION 1
CONTROL j
I
MODEL
HASTE TYPE
ANNUAL
THROUGHPUT
(Mg/yr)
UNCONTROLLED
EMISSIONS
(Mg/yr)
d
EMISSION
REDUCTION
(Mg/yr)
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
                                 TANK TREATMENT
    COVERED QUIESCENT TREATMENT TANK (T01E) - 20,000 gal tank
Internal
Floating
Roof



Vent to
Existing
Control
Device



Vent to .
Carbon '
Canister"



Aq Sludge
Dilute Aq
Org Liquid
Org Sludge/S lurry
Two-Phase Aq/Org
Aq Sludge
Di lute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge
Dilute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
Two-Phase
28,000
28,000
28,000
28,000
28,000
28,000
28,000
28,000
28,000
28,000
t 28,000
28,000
28,000
28,000
28,000 |
0.24
4.60
1.19
1.40
1.94
0.24
4.60
1.19
1.40
1.94
0.24
4.60
1.19
1.40
1.94
0.20
3.40
0.98
1.15
1.51
0.23
4.37
1.13
1.33
1.84
0.23
4.37
1.13
1.33
1.84
$11,380
$11,380
$11,380
$11,380
$11,380
$1,600
$1,600
$1,600
$1,600
$1,600
$1,050
$1,050
$1,050
$1,050
$1,050
$3,600
$3,600
$3,600
$3,600
$3,600 '
$300
$300
$300
$300
$300
$12,740
$185,870
$50,410
$5,900
$79,780
See notes at end of table.
(continued)
                                    C-70

-------
     TABLE  C-6.   SUMMARY  OF TSDF MODEL UNIT ANALYSIS RESULTS'
b
EMISSION
CONTROL



MODEL
WASTE TYPE


,"*"""- ' '"Ji=a
! ANNUAL
j THROUGHPUT
! (Mg/yr)
. 	 TAl
c!
UNCONTROLLED !
EMISSIONS !
(Mg/yr) !
« TREATMENT 	
d!
EMISSION !
REDUCTION \
(Mg/yr) !

i
TOTAL !
CAPITAL !
INVESTMENT |


TOTAL
ANNUAL
COSTS

— COVERED Q
Internal
Floating
Roof



Vent to
Existing
Control
Device



Vent to
Fixed Bed
Carbon
Adsorber



UIESCENT TREATMENT
Aq Sludge
Dilute Aq
Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge
DlluteAq

Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
Aq Sludge

Dilute Aq

Org Liquid
Org Sludge/Slurry
Two-Phase Aq/Org
TANK (T01F)
290,000
290,000
290,000
290,000
290,000
290,000
290,000

290,000
290,000
290,000
290,000

290,000

290,000
290,000
290,000
- 210,000 gal t
2.45
47.23
11.05
14.32
19.89
2.45
47.23

11.05
14.32
- 19:89
2.45

47.23

11.05
14.32
19.89
ank —
2.01
34.95
9.06
11.74
15.52
2.32
44.87

10.49
13.60
18.90
2.32

44.87

10.49
13.60
18.90

$19,660
$19,660
$19,660
$19,660
$19,660
$1,600
$1,600

$1,600
$1,600
$1,600
$74,180

$74,180

$74,180
$74,180
$74,180

$5,810
$5,810
$5,810
$5,810
$5,810
$300
$300

$300
$300
$300
$52,310

$52,310

$52,310
552,310
$52,310
See notes at end of table.
(continued)
                                 C-71

-------
       TABLE C-6.   SUMMARY  OF TSDF MODEL  UNIT ANALYSIS  RESULTS^
EMISSION
CONTROL

t
! MODEL
j WASTE TYPE
i
i
ANNUAL
THROUGHPUT
(Mg/yr)
Q
UNCONTROLLED
EMISSIONS
(Mg/yr)
d!
EMISSION !
REDUCTION i
(Mg/yr) |
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
—————— IMIUV ini.Himi.iii — — — —
— UNCOVERED AERATED/AGITATED TREATMENT TANK (T01G) - 28,500 gal tank —
ASP+FBCA | Aqueous 240,000 870 827 $124.000
i Sludge
! Dilute 240,000 130 124 $125,000
! Aqueous-1
$66,600
$94,800
— UNCOVERED AERATED/AGITATED TREATMENT TANK (T01H) - 423,000 gal tank —
ASP+FBCA J Aqueous 2,800,000 | 10,600 10,070 $732,000
j Sludge j
! Dilute 2.80G
i Aqueous-1
,000 4,600 4,370 $732,000
i
$607,000
$607,000
See notes at end of table.
(continued)
                                C-72

-------
    TABLE C-6.   SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS'
b !
EMISSION !
CONTROL |
i
MODEL
HASTE TYPE
! ANNUAL
i THROUGt-PUT
! (Mg/yr)
c!
UNCONTROLLED !
EMISSIONS !
(Mg/yr) i
d !
EMISSION !
REDUCTION i
(Mg/yr) !
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
	 bUKrALL IMfUUNUMtW muumuii 	
— QUIESCENT TREATMENT IMPOUNDMENT (T02A) - 71,300 gal Impoundment —
ASP+FBCA ! Aqueous
! Sludge
Dilute
Aqueous-1
Two-Phase
Aqueous/Organic
MEMBRANE Aqueous
Sludge
Dilute
Aqueous-1
Two-Phase
Aqueous/Organic
200,000 301 286 j $181,200 | $85,300
!
200,000 135 128 $
200,000 265 252 i
200,000 301 256
200,000 135 115
200,000 265 225
179,800 $83,300
i
H79.800 $83,300
i
$14,760 $8,000
t
i
$14,760 ! $8,000
i
$14,760 j $8;000
t
	 QUIESCENT TREATMENT IMPOUNDMENT (T02B) - 71,300 gal irapounctaent —
ASP+FBCA ! Aqueous
! Sludge
Dilute
Aqueous-1
i Two-Phase
! Aqueous/Organic
MEMBRANE Aqueous
Sludge
Dilute
Aqueous-1
Two-Phase
Aqueous/Organic
20,000 191 j 181 j
!
20,000 53 50
20,000 65 62
i '
20,000 191 162
i
i
20,000 53 45
i
20,000 65 55
i
$176,900 $79,200
$171,800 $72,600
$171,800 $72,600
t
$14,760 $8,000
$14,760 $8,000
$14,760 $8,000
See notes at end of table.
(continued)
                                 C-73

-------
        TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS3
b
EMISSION
CONTROL
MODEL
WASTE TYPE
ANNUAL
™OUGH=UT
(Mg/yr)
UNCONTROLLED
EMISSIONS
(Mg/yr)
d !
EMISSION !
REDUCTION |
(Mg/yr) i
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
	 ouni i
— QUIESCENT TREATMENT IMPOUNDMENT (T02C) -
ASP+FBCA

Aqueous
Sludge
Dilute
Aqueous-1
990,000
990,000
Two-Phase 990,000
Aqueous/Organic
MEMBRANE

! Aqueous
! Sludge
Dilute
Aqueous-1
990,000
990,000
! Two-Phase j -990,000
[Aqueous/Organic!
— QUIESCENT TREATMENT IMPOUNDMENT (T02D) -
ASP+FBCA


Aqueous
Sludgu

Dilute
Aqueous-1
99,000 !
i
i

99,000
1
j Two-Phase ! 99,000
Aqueous/Organic!
MEMBRANE


Aqueous
Sludge
Dilute
Aqueous-1
Two-Phase
Aqueous/Organlcj
99,000
99,000
99,000
1UC IWlAJNUMtNl IKtAIMtNT 	
- 713,000 gal impoundment —
1.400
700
1,320
1,400
700
1,320
713,000 gal
946

269
326
946
269
326
1,330
665
1,254
1190
595
1122
Impoundment —
899
1
I
256
i
i
i
310
i
804
229
277
- $280,600
$277,500
$277,500
$57,000
$57,000
$57,000

$262.800

$237,500
I
$237,500 1
i
i
$57,000
$57,000
$57,000
$147,900
$147,900
$147,900
$19,700
$19,700
$19,700

$128,200

$97,600
$97,600
$15,800
$15,800
$15,800
See notes at end of table.
(continued)
                                 C-74

-------
     TABLE  C-6.   SUMMARY  OF TSDF MODEL  UNIT  ANALYSIS  RESULTS'
b
EMISSION MODEL ANNUAL
CONTROL ! WASTE TYPE THROUGHPUT
! (Mg/yr)
CttDI
— QUIESCENT TREATMENT IMPOUNDMENT (T02E)
ASP+FBCA Aqueous 608.000
Sludge
Dilute 608,000
Aqueous-1
Two-Phase 608,000
Aqueous/Organic
MEMBRANE Aqueous ! 608,000
Sludge !
Dilute 608,000
Aqueous-1
Two-Phase i 608,000
Aqueous/Organlcj
UNCONTROLLED
EMISSIONS
(Mg/yr)
:ACE IMPOUNDMENT
- 8,720,000 gal
5,530
1,710
2,040
5,530
1,710
2,040
— QUIESCENT TREATMENT IMPOUNDMENT (T02F) - 8,720,000 gal
ASP+FBCA Aqueous 302,000
Sludge
Dilute 302,000
Aqueous-1
Two-Phase 302,000
Aqueous/Organic
MEMBRANE Aqueous 302,000
Sludge
Dilute 302,000
Aqueous-1
Two-Phase 302,000
Aqueous/Organic
4,030
990
1,120
i
4,030
990
1,120
d
EMISSION
REDUCTION
(Mg/yr)
TREATMENT -
Impoundment
5,254
1,625
1,938
4,701
1,454
1,734
Impoundment
3,829
941
1,064
3,426
842
952
i
TOTAL
CAPITAL
INVESTMENT

—
$636,600
$500,000
$500,000
! $300,070
$300,070
i
! $300,070
I 1
lar-i-i-ir'
$577,900
$461,500
$461 ,500
i
$300,070
$300,070
$300,070
ZS=== =====: =SR=S3=3
TOTAL
ANNUAL
COSTS

$395,200
$224,900
$224,900
$10,800
$10,800
$10,800

$321,000
$169,300
$169,300
$66,500
$66,500
$66,500
See notes at end of table.
(continued)
                                 C-75

-------
         TABLE C-6.   SUMMARY OF TSDF  MODEL  UNIT  ANALYSIS  RESULTS3
EMISSION ! MODEL
CONTROL ! HASTE TYPE
i
i
ANNUAL
THROUGHPUT
(Mg/yr)
c
UNCONTROLLED
EMISSIONS
(Mg/yr)
d
EMISSION
REDUCTION
(Mg/yr)
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
                                      SURFACE IMPOUNDMENT TREATMENT
 — AERATED/AGITATED TREATMENT  IMPOUNDMENT (T02G) - 7.1,300 gal Impoundment —
   ASP+FBCA
    Aqueous
    Sludge

    Dilute
   Aqueous-1

   Two-Phase
            .{Aqueous/Organic!
200,000


200,000


200,000
                                                  683


                                                  760


                                                  763
               649



               722



               725
$196,200 j    $103,000
$199,200


$199,200
                                                                        $107,000


                                                                        $107,000
    AERATED/AGITATED TREATMENT IMPOUNDMENT (T02H) - 71,300 gal  Impoundment —
  ASP+FBCA

    Aqueous
    Sludge

    Dilute
   Aqueous-1
            }   Tiro-Phase
            !Aqueous/Organic
 20,000 j
        i

 20,000 !
                    20,000 !
  302


   78


   77
                                                              287 !     $181,300  |
                               73
$179,000 !
         i


$179,000 |
                                                                         $9.000


                                                                         $8,000


                                                                         $8,000
    AERATED/AGITATED TREATMENT IMPOUNDMENT (T02I) - 713,000 gal  Inpoundinent —
  ASP+FBCA
    Aqueous
    Sludge

    Dilute
   Aqueous-1

   Two-Phase
Aqueous/Organic
990,000 i
        j

990,000 |
                                990,000
6,530


3,800



3,860
                                                            6,204


                                                            3,610
$481,000 j   $404,000
         I


$376,000 j   $266,000
                            3,667       $376,000  j   $266,000
— AERATED/AGITATED TREATMENT IMPOUNDMENT (T02J) - 713,000 gal impoundment 	
  ASP+FBCA
    Aqueous
    Sludge

    Dilute
   Aqueous-1

   Two-Phase
Aqueous/Organic
                    99,000



                    99,000



                    99,000
See notes at  end  of table.
                                                1,920
                                                  390 !
                                                  380 !
                            1,824



                              371



                              361
                       $305,000



                       $298,000



                       $293,000
            $177,000



            $122,000



            $122,000
                                                                (continued)
                                           C-76

-------
     TABLE C-6.   SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS'
b
EMISSION
CONTROL
i
MODEL
HASTE TYPE
i
ANNUAL
TffiOUGtfHJT
(Mg/yr) !
C
UNCONTROLLED
EMISSIONS
(Mg/yr)
d!
EMISSION
REDUCTION
(Mg/yr)
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
fllRFAPF IMPffllNTIMFNT TRFATMFNT 	
	 AERATED AGITATED TREATMENT IMPOUNDMENT (T02K) - 8,720,000 gal Impoundment —
ASP+FBCA





Aqueous !
Sludge !
1
Dilute
Aqueous-1
Two-Phase
Aqueous/Organic
608,000

608,000

608,000

12,160

2,300

2,400

11,552

2,185

2,280

$777,000

$512,000

$512,000

$693,000

$237,000

$237,000
i
— AERATED/AGITATED TREATMENT IMPOUNDMENT (T02L) - 8,720,000 gal impoundment —
ASP+FBCA




| Aqueous
Sludge
. Di lute
Aqueous-1
Two-Phase
302,000

302,000

302,000
6,520
i
! 810

1,200
6,194

770

1,140
$675,000

$460,000

$480,000
Aqueous/Organic!
$445,000

$169,000

$169,000
i
See notes at end of table.
(continued)
                                  C-77

-------
       TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS3
b
EMISSION
CONTROL
MODEL
HASTE TYPE
ANNUAL
THROUGHPUT
(Mg/yr)
! c
j UNCONTROLLED
! EMISSIONS
! (Mg/yr)
d!
EMISSION !
REDUCTION !
(Mg/yr) |
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
— HASTE FIXATION (Fixation
Mixer
Baghouse,
&FBCA

Aqueous
Sludge
i
Two-Phase
! Aqueous/Organic
— HASTE FIXATION (Fixation
Mixer
Baghouse,
& FBCA

Aqueous
Sludge

Two-Phase
Aqueous/Organic
— HASTE FIXATJON (Fixation
* Mixer
Baghouse.
& FBCA ,
i
i
Aqueous
Sludge

Two-Phase
Aqueous/Organic
————— nnoiL i IAMI IUM 	
Pit A) —
17,000 51.0

17,000 51.0
Pit B) —
117,000 351.0 i
i

117,000 351.0
i
Pit C) — «
167,000 501.0
i
i
167,000 501.0
i

48.0 j $464,000 $228,000
i
50.0 $464,000 $228,000
i

330 $572,000 $213,000

300 $572,000 $213,000

480 $616,000 $277,000
! !
500 $616,000 $277,000
i
See notes at end of table.
(continued)
                                C-78

-------
     TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS'
b
EMISSION
CONTROL


MODEL
WASTE TYPE

!
ANNUAL !
ThROUGtfHJT!
(Mg/yr) !
c!
UNCONTROLLED i
EMISSIONS i
(Mg/yr) !
d
EMISSION
REDUCTION
(Mg/yr)

TOTAL
CAPITAL
INVESTMENT

TOTAL
ANNUAL
COSTS
— ACTIVE LANDFILL (D800) - 1
Dally Earth Aqueous !
Cover Sludge !
Two-Phase !
Aqueous/Organic!
— ACTIVE LANDFILL (D80E) - 3
Dally Earth j Aqueous !
Cover j Sludge !
! Two-Phase !
j Aqueous/Organic!
— ACTIVE LANDFILL (D80F) - 5
Dally Earth ! Aqueous !
Cover ! Sludge !
j Two-Phase !
i Aqueous/Organic j
	 LHIUM ILL UIOI UOML. 	
acre —
16,650 ! 100.6 ! 11.1
i t
i i
16,650 ! 86.1 j 9.5
.5 acres —
116,500 i 358.1 39.4
i
i
116,500 j 299 32.9
acres —
166,500 j 510.9 j 56.2 |
i i i
166,500 j 427 j 47 j
! ! !

$0 $44,800
$0 $44,800

$0 ! $313,400
i
$0 ! $313,400
1

$0 | $447,300
$0 ! $447,900
I
1
See notes at end of table.
(continued)
                                  C-79

-------
       TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS*
sBi? | wjs&t \ ™*SUT 1 1 sal
! ! (Mg/yr) | (Mg/yr) j (Mg/yr) j
— CLOSING LANDFILL (D80G) -
C.Landf 1 1 1 | Aqueous
30 all-HOPE j Sludge
i Two-Phase
[Aqueous/Organic
C.Landf 1 1 1 j Aqueous
100BU-HQPEJ Sludge
! Two-Phase
i Aqueous/Organic
— CLOSING LANDFILL (D80H) -
C.Landflll j Aqueous !
SOall-HOPE | Sludge i
! Two-Phase ,'
! Aqueous/Organic!
C.Landflll j Aqueous !
lOOall-HOPEi Sludge \
! Two-Phase |
i Aqueous/Organic,1
— CLOSING LANDFILL (D80I) -
C.Landflll | Aqueous !
30BII-HDPE j Sludge i
! Two-Phase |
[Aqueous/Organic!
C.Landflll | Aqueous J
100HII-HDPE! Sludge !
I " Two-Phase J
! Aqueous/Organic!
LAWDFI
• 1 acre —
16,650 j
16,650 |
i
i
16,650 j
i
16,650 j
i
3.5 acres —
116,500
116,500
116,500
116,500
5 acres —
166,500
166,500
166,500
166,500
!" * • « MmSM.^. 1- « _ -^S£=J


0.020
0.6
0.020
0.6

0.068
2.09
0.068 '
2.09

0.0973 j
t
2.89 !
i
0.0973 j
i
2.89 i
t


0.019 j
0.29 |
i
i
0.019 i
0.51 |
i

0.0678
1.03
0.0679
1.77

0.0970 |
i
i
1.42 j
0.0972 j
i
2.45 1
i
===^;gjii-i— _ T--JI.
TOTAL
CAPITAL
INVESTMENT

$17,260
$17,260
$44,490
$44,490

$60,370
$60,370
$155,720 '
$155,720

$86,250
$88,250
$222,450
$222,450
TOTAL
ANNUAL
COSTS

$2,000
$2,000
$6,000
$6,000

$9,000
$9,000
$23,000
$23,000

$13,000
$13,000
$33,000
$33,000
See notes at end of table.
(continued)
                                  C-80

-------
     TABLE C-6.   SUMMARY OF  TSDF MODEL UNIT ANALYSIS RESULTS*
       b  i
 EMISSION   !
 CONTROL   !
)EL
TYPE
ANNUAL
THROUGHPUT
(Mg/yr)
c
UNCONTROLLED
EMISSIONS
(Mg/yr)
d
EMISSION
REDUCTION
(Mg/yr)
TOTAL
CAPITAL
INVESTMENT
TOTAL
ANNUAL
COSTS
                                             e
                        	 CONTAINER LOADING 	
— DRUM LOADING - 200 drunts/yr
Submerged
Fill Pipe









Aqueous
Sludge

Dilute
Aqueous- 1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
50


40

40

60

40

0.0018 |


0.0357

0.0068

0.0175

0.0150

0.0012


0.0232
.
0.0044

0.0114

0.0098

$390

I
$390

$390

$390

$390

$70


$70

$70

$70

$70

 — DRUM LOADING - 2,200 drums/yr —
Submerged
Fill Pipe


•
.
-




Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
560

450

440

610

440

0.0195

0.3900

0.0743
•
0.1910

0.1640

0.0127

0.2535

0.0483

0.1242

0.1066

$390
.
$390

$390
-
$390

$390

$70

$70

$70

$70

$70

    TANK TRUCK LOADING —
Submerged
Fill Pipe








Aqueous
Sludge
Dilute
Aqueous-1
Organic
Liquid
Organic
Sludge/Slurry
Two-Phase
Aqueous/Organic
521

423

413

499

490

0.0045

0.0908
.
0.0169
'
0.0446

0.0385

0.003

0.059

0.011

0.029

0.025

$390

$390

$390

$390

$390
±==s=:==:=s===s
$70

$70

$70

$70

$70

 See  notes  at end  of table.
(continued)
                                     C-81

-------
     TABLE C-6.   SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS9 (continued)

 aThis table summarizes  the control  costs  and  emission  reductions  by  process
  unit for controlling organic  air emissions from hazardous waste  treatment
  storage,  and disposal  facilities (TSDF).   The  control  costs and  achievable
  emission  reductions  were  estimated through a model  unit  analysis  utilizing  a
  variety  of diverse yet representative TSDF process  model units, model waste
  compositions or forms,  and applicable control  technologies.  The  costs  (in
  terms of  5/Mg  of waste throughput)  were  then used  to  develop the  control
  technology and cost  file  (Appendix D,  Section  D.2.5)  that is used in
  combination  with the TSDF Industry Profile (Appendix  D,  Section D.I.3) and
  the  waste characterization data  base  (Appendix  D, Section D.I.4)  to estimate
  nationwide cost  impacts for alternative  control  strategies.

  The  model  wastes used  in  the determination of control  costs and emission
  reduction  in the model unit analysis  may  not necessarily be representative-of
  all  actual waste streams  processed  at  existing  facilities.  However, to the
  extent possible, the composition and  quantities of the actual waste streams
  processed  at existing facilities were  used in estimating nationwide emissions
  and emission reductions resulting  from the alternative control  strategies.

  Please note that all  costs presented  in this table are in January 1986
 dollars.                                                         J

bl-  Carbon Adsorption—Two different carbon adsorption systems  were examined
     for application  as  control devices.  One system involves the use of
     fixed-bed,  regenerate carbon adsorption  units (FBCA);  the  other involves
     use of disposable carbon canisters.  Both carbon canisters  and fixed bed
     regenerate carbon  systems were costed for each of the model  unit/waste
     form  cases; the  less expensive system was selected for application.   The
     fixed-bed carbon  system's  operating costs include the regeneration and
     eventual  replacement and disposal  of spent  carbon; carbon canister's
     operating costs  include carbon canister replacement and  disposal.   Carbon
     adsorption  can reasonably  be expected to  achieve a 95-percent control
     efficiency  for most organics under a  wide variety of  stream  conditions
     provided  (1)  the  adsorber  is supplied with  an adequate quantity  of hiqh
     quality activated carbon,  (2)  the gas stream receives appropriate
     conditioning (e.g.,  cooling,  filtering) before  entering  the  carbon bed,
     and 13) the carbon  beds are regenerated or  replaced before breakthrough.

     Internal  Floating Roofs—Emission  reductions for internal floating roofs
     relative  to a fixed-roof tank were estimated by  using the emission models
      5CcDA?d ln  APPe"dix  c- Section C.I.1.4.3  (fixed  roof tank emissions)
    and EPA's Compilation  of Air  Pollutant Emission  Factors  (AP-42)
    Estimated emission  reductions ranged  from 74 to 82  percent.  The varia-
    tion in emission  reductions  is  attributable  to differences in  composition
    and concentrations  of  model wastes.

    Internal floating roofs  are applied to uncovered vertical tanks  in
    conjunction with  a fixed roof to suppress the uncovered  tank organic
    emissions.  For this combination,  the  emission reductions achievable are
    a combination of the reduction  from application of the fixed roof to the
2.
                                                                  (continued)
                                   C-82

-------
   TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS9 (continued)

    uncovered tank, plus application of an internal floating roof to a fixed-
    roof tank.  The range of emission reductions achievable based on
    combination of the fixed roof with the internal floating roof is 96 to
    99.

3   Existing Control Device—Venting organic emissions to an existing control
    device -is assumed to achieve an overall emission reduction of 95 percent;
    this includes both capture and control efficiencies.

4.  Fixed Roof—Emission reductions for application of fixed roofs to
    uncovered tanks ranged from 25 to greater than 99 percent depending on
    waste form for both storage and treatment tanks.

5   Membrane—Floating synthetic membranes are applicable to quiescent
    impoundments and uncovered storage tanks.  Emission reductions are
    determined by  the fraction of surface  area covered and  by the perme-
    ability  of the membrane.  An emission  reduction of 85 percent was used
    for  floating synthetic membranes  for purposes  of estimating  emission
    reductions from membrane-covered  impoundments.

6   ASP—This control alternative involves installing  an  air-supported
    structure  (ASP) and  venting emissions  to  a carbon adsorption system.  The
    efficiency of  air-supported structures in reducing or  suppressing emis-
    sions  is determined  by the combined  effects  of the capture efficiency of
    the  structure  and the removal efficiency  of  the control device.   An  over-
    all  control  efficiency of 95  percent is used for  air-supported  structures
    vented  to carbon  adsorber.

 7   HOPE—In this  control technique,  flexible covers  are  used  to suppress or
    TTiTt  organic  emissions  from  area sources.   A typical  cover  material  is
    30-mil  high-density polyethylene (HOPE).  For the purposes of estimating
    emission reductions,  control  efficiencies of 0, 49.3,  and  99.7  percent
    were used for  30-mil  HOPE covers, depending on characteristics  of the
    waste  (i.e.,  permeability).   Emission reductions  of 0, 84.8, and 99.9
    percent were selected for the model  wastes  with a 100-mil  HOPE cover.
    The variations in emission reductions are attributable to differences in
     composition  and concentrations  of the model  wastes.

^Uncontrolled emissions were estimated for each  model  unit and waste type
 using the appropriate TSDF air emission models  as described in Section C.I;
 the model  unit design and operating parameters  described in Section C.Z.I;
 and the waste compositions listed in Appendix C, Table C-5.

^Emission reductions achievable through application of the  emission control
 technologies are calculated on the basis of the control efficiencies
 presented in Chapter 4.0.  These emission reductions can be grouped into
 three broad categories based on the technologies  involved:

      (1)  Suppression Controls-- Emission  reduction are achieved by controls
          that contain the organics within a  confined area  and prevent or
          limit volatilization of the organics.  Unless used in  combination
          with add-on control devices, the organics may be  emitted from a

                                                                    (continued)
                                    C-83

-------
TABLE C-6.  SUMMARY OF TSDF MODEL UNIT ANALYSIS RESULTS* (continued)
 (2)
         downstream TSDF waste management process.  Suppression devices
         include  internal floating roofs for covered or closed tanks and
         floating synthetic membranes for impoundments.

         Add-on Controls—Emission reductions are achieved by add-on controls
         that adsorb, condense, or combust the volatile organics and as a
         I?SUItupUevenJ their release to the atmosphere.  Examples include
         nxed-bed carbon adsorbers,  condensers, thermal or catalytic
         incinerators.

    total capital investment and total annual  costs for the Container

rail tank°car       ^ ^ "^ f°r drUm Ioad1ng'  tank truck loading,  and
                              C-84

-------
of different compositions and forms are managed in that unit.  The table
also shows that control costs for certain controls are independent of waste
composition, e.g., fixed roof for storage tanks and floating synthetic
membranes.  At the opposite extreme, the costs for fixed-bed carbon
adsorption controls (e.g., those applied to uncovered, aerated treatment
tanks model unit T01G) are highly sensitive to composition;  i.e., bed size
is a function of the level or quantity of uncontrolled emissions.
     The emission reductions reported in Table C-6 are achieved through
application of control technologies that can be classified  into two broad
categories  based on the control mechanisms.  Suppression controls contain
the organics within a  confined  area and prevent or limit volatilization.
Add-on  controls are typically conventional air pollution control devices
that adsorb, condense, or  thermally destroy the volatile organics to
prevent release to the atmosphere.
     The footnotes to  Table  C-6 explain  an important  point  about the
reported emission  reductions.   Controls,  such  as  a fixed  roof  applied to  a
storage tank,  suppress organic  emissions  from  that tank by  the amount
 indicated in  the  table.   The emissions  prevented  by  installation  of a fixed
 roof may escape  from  the waste  at some downstream waste processing  step
 unless  emissions  from that downstream process  are also controlled.   The
 emission reductions  achieved through  suppression  controls are truly
 emission reductions  only if the suppressed emissions are  prevented from
 escaping the waste processes at other downstream processing steps.   Add-on
 controls (such as carbon adsorption and vapor incineration) and/or biolog-
 ical  decay to less volatile compounds are the principal  approaches to avoid
 ultimate discharge to the atmosphere.
 C.3
 1.
 2.
REFERENCES
Research Triangle Institute.  Hazardous Waste Treatment Storage, and
Disposal Facilities:  Air Emission Models, Draft Report.  Prepared for
U.S. Environmental Protection Agency.  Office of Air Quality Planning
and Standards.  Research Triangle Park, NC.  March 1987.
U.S. Environmental Protection Agency.  Hazardous Waste Treatment,
Storage, and Disposal Facilities (TSDF)—Air Emission Models.
Publication No. EPA-450/3-87-026.  Research Triangle Park, NC.  Office
of Air Quality Planning and Standards.  December 1987.  p. 4-41 to
4-49.
                                      C-85

-------
 3.   Springer, C., P. D. Lunney, and K. T. Valsaraj.  Emission of Hazardous
      Chemicals from Surface and Near Surface Impoundments to Air.  U.S
      Environmental Protection Agency, Solid and Hazardous Waste Research
      Division.  Cincinnati, OH.  Project Number 808161-02.  December 1984
      p. 3-4 to 3-16.

 4.   Mackay, D.,  and A. Yeun.  Mass Transfer Coefficient Correlations for
      Volatilization of Organic Solutes from Water.  Environmental Science
      .and Technology.  17:211-217.  1983.
 5.    Hwang,  S. T.  Toxic Emissions from Land Disposal Facilities.
      mental  Progress.  1.:46-52.  February 1982.

 6.    Reference 5, p.  46.
                    Environ-
 6.5.  Chemical  Manufacturers Association.   Comments of the Chemical
      Manufacturers Association on the Environmental  Protection Agency
      Document  "Hazardous Waste TSDF - Background Information for Proposed
      RCRA Air  Emission Standards - Volumes I  and II."  Washington  D.C
      July 11,  1988.   105 p.                                      '

 7.    Memorandum from Coy,  D.,  RTI,  to Docket.   January 1989.  Investigation
      of  and  recommendations for revisions  to  aerated model  unit parameter
      used in the Source Assessment Model.
8.   Reference  5.

9.   Crank, J.  The Mathematics  of  Diffusion.
     Press.  1970.  p. 45-47.

10.  Reference  1, p. 6-1.
London, Oxford University
11.  Farmer, W. J., M. S. Yang, J. Letey, W. F. Spencer, and M. H. Roulier.
     Land Disposal of Hexachlorobenzene Wastes:  Controlling Vapor Movement
     in Soils.  Fourth Annual Research Symposium.  U.S. Environmental Pro-
     tection Agency.  Publication No. EPA-600/9-78-016.  August 1978.

12.  Millington, R. J., and J. P. Quirk.  Permeability of Porous Solids
     Trans. Faraday Society.  57:1200-1207.  1961.

13.  Reference 1, p. 6-40.

14.  Acurex Corporation.  Volatile Emissions from Stabilized Waste in
     Hazardous Waste Landfills.  Prepared for US EPA/AEERL.  Research
     Triangle Park, NC.  Contract No. 68-02-3993.   September 1987.

15.  U.S.  Environmental Protection Agency.  Compilation of Air Pollutant
     Emission Factors.   AP-42, 4th ed.,  Section 4.4.   Transportation and
     Marketing of Petroleum Liquids.   Office of Air Quality Planning and
     Standards.  Research Triangle Park,  NC.  September 1985.   13 pp.
                                    C-86

-------
16.
18.


19.
U.S. Environmental Protection Agency.  Assessing the Release and Costs
Associated with Truck Transport of Hazardous Wastes.  PB 84-224-468
(Contract No. 68-01-0021).  Washington, DC.  January 1984.  p. 8.
17.  Reference 16.
20.




21.

22.




23.
Shen, T. T.  Estimating Hazardous Air Emissions from Disposal Sites.
Pollution Engineering.  31-34.  August 1981.

GCA Corporation.  Air Emissions of VOC from Waste Piles at Hazardous
Waste Treatment, Storage, and Disposal Facilities:  Draft Technical
Note    Prepared for U.S. Environmental Protection Agency, Office or
Air Quality Planning and Standards.  Research Triangle Park, NC.
Contract No. 68-01-6871.  August 7,  1985.

U S  Environmental Protection Agency.  Compilation of Air Pollutant
Emission Factors.  AP-42, 4th ed., Section  4.3.   Storage of  Organic
Liquids.  Office of Air Quality Planning  and Standards.  Research
Triangle Park,  NC.  September 1985.  p. 4.3-8.

Reference 20,  p. 4.3-5.

U S  Environmental Protection Agency.  Control  of Volatile  Organic
Compound  Leaks from Synthetic Organic  Chemical  and Polymer  Manufactur-
ing  Equipment.  Research  Triangle  Park,  NC.  Publication No. EPA-
450/3-83-006.   March  1984.   p.  2-21.

U  S.  Environmental  Protection Agency.  Compilation of Air  Pollutant
 Emission  Factors.   AP-42,  4th ed.   Office of Air Quality Planning  and
Standards.   Research  Triangle Park,  NC.   September 1985.   817 p.
 24.   Reference 22,  p.  2-20.

 25.   Reference 16,  p.  8.

 26.   Memorandum from Branscome, M. R., RTI, to Docket.  November 13, 1987.
      Westat data used to develop model units for surface impoundments and
      tanks.

 27.   U.S. Environmental Protection Agency.  EPA Design Manual:  Municipal
      Wastewater Stabilization Ponds.  Publication No. EPA-625/1-83-015.
      October 1983.  p. 3.

 28   Metcalf and Eddy,  Inc.  Wastewater Engineering.  New York, McGraw-
      Hill.  1972.  p. 557.

 29.  Reference 28, p. 519.

 30.  U.S. Environmental Protection Agency.  Hazardous Waste  TSDF Waste
      Process Sampling.  Report  No. EMB/85-HWS-3.  October 1985.  p.  1-11.
                                      C-87

-------
  31.   U.S.  Environmental  Protection Agency.   Evaluation  and  Selection  of
       Models for Estimating Air Emissions  from Hazardous Waste  Treatment
       Storage,  and Disposal  Facilities.  Publication  No.  EPA-450/3-84-020
       December  1984.   p.  69.

  32.   Reference 31, p.  67.

  33.   Reference 31, p.  67.

  34.   Reference 31, p.  67.

  35.   Eckenfeld, W., M. Goronszy, and T. Quirk.  The Activated  Sludge
       Process:   State of  the Art.   CRC Critical Reviews  in Environmental
       Control.  15(2):148.  1984.

 36.   Reference 2, p. 419.

 37.   Reference 28.

 38.   Reference 26.

 39.  Reference 29.

 40.  Memorandum from Thorneloe, S., EPA/OAQPS, to Durham, J.,  EPA/OAQPS.
      February 12,  1986.  Land treatment data base.

 41.  Environmental Research and Technology.   Land Treatment  Practices  in
      the Petroleum Industry.   Prepared  for American Petroleum  Institute.
      Washington, DC.   June 1983.   p. 1-2.

 42.  Radian Corporation.   Field Assessment of Air Emissions  and Their  Con-
      trol  at a  Refinery Land  Treatment  Facility.   Volume I.  Prepared  for
      U.S.  EPA/ORD/HWERL.   Cincinnati, OH.   EPA Contract  No.  68-02-3850.
      September  1986.   p.  43.

 43.   U.S.  EPA/ORD/RSKERL.  Evaluation of Volatilization  of Hazardous Con-
      stituents  at  Hazardous Waste Land  Treatment  Sites.   Ada, OK.   Publica-
      tion No. EPA/600/2-86/061, NTIS #PB86-233 939, August 1986.   p. 55.

 44.   Trip Report.  Goldman, Leonard, RTI,  with Chemical  Waste Management
      Sulphur, LA.  September 12, 1986.

 45.   Telecon.  Goldman, Leonard, RTI, with Boyenga, Dave, MBI Corporation
      Dayton, OH.  November 20,  1985.

46.   Telecon.  Goldman, Leonard, RTI, with Webber, Emlyn, VFL Technology
      Corporation, Malvern, PA.  November 12, 1985.

47.  Telecon.  Massoglia, Martin, RTI,  with Webber, Emlyn, VFL  Technology
     Corporation, Malvern, PA.  January 13, 1987.
                                   C-88

-------
48.  Telecon.  Goldman, Leonard, RTI, with Hannak,  Peter,  Alberta Environ-
     mental Center.  Fixed waste.  April 10, 1986.
49.

50.


51.



52.



53.



54.


55.

56.



 57.
Reference 48.

Shen, T. T.  Estimating Hazardous Air Emissions from Disposal Sites.
Pollution Engineering.  31-34.  August 1981.

Research Triangle Institute.  Performance of Clay Caps and Liners for
Disposal Facilities.  Prepared for U.S. Environmental Protection
Agency.  Cincinnati, OH.  EPA Contract No. 68-03-3149.  March 1983.

Telecon.  Clark, Chris, RTI, with Borden, Roy, Department of Civil
Engineering, North Carolina State University, Raleigh, NC.  April ZU,
1988.   Soil  porosity.

Geraghty, J. J., D. W. Miller, F. Vander  Leeden, and  F. L. Troise.
Water Atlas  of  the United States.  Port Washington,  NY, Water Informa-
tion Center, 1973.  Plate 30.

Telecon.  Goldman, Leonard, RTI, with  Hughes, John,  National Climatic
Center,  Asheville, NC.  May 15,  1986.
                                                             EPA.   TSDF
    Reference  54.

    Memorandum from  Eichinger,  Jeanne,  GCA,  to  Hustvedt,  K.  C.
    Model  Source  Parameters  and Operating  Practices  Database.
    September  6,  1985.   7  p.

    Engineering Science.   National  Air Emissions  from Storage  and Handling
    Operations at Hazardous  Waste Treatment, Storage,  and Disposal  Facili-
    ties.   Prepared  for U.S.  Environmental Protection Agency,  Office of
    Air Quality Planning and Standards.  Research Triangle Park,  NC.
    Contract No.  68-03-2171,  Task,  SBE06.   January 1985.

58. Telecon.  Yang,  S., RTI,  to Accurate Industries, Inc., Williamstown,
    NJ.  Dumpster dimensions.  November 19, 1985.
 59.
 60.
 GCA Corporation.  Air Emission Estimation Methods for Transfer, Stor-
 age, and Handling Operations.  Draft Technical Note.  Prepared for
 U.S. Environmental Protection Agency, Office of Air Quality Planning
 and Standards.  Research Triangle Park, NC.  Contract No. 68-01-6871.
 August 1985.

 U.S. Environmental Protection Agency.  Compilation of Air Pollutant
 Emission Factors.  AP-42, 4th ed.t Section 4.4.  Transportation and
 Marketing of  Petroleum  Liquids.  Office of Air Quality Planning and
 Standards.  Research Triangle Park,  NC.  September 1985.  13 pp.
                                      C-89

-------
61.  Reference 33.

62.  Reference 56.

63.
64.
65.
      Memorandum from Deerhake,  M.  E.,  RTI,  to Docket.   November 5,  1987.
      Use of the U.S. EPA hazardous waste data management system to  select
      model  drum storage units.

      United States  Environmental  Protection Agency.   Benzene  Fugitive Emis-
      sions—Background  Information for Promulgated Standards.   EPA-450/3-
      80-032b.   Research Triangle  Park,  NC.   June 1982.   p.  2-94.

      Radian Corporation.   Characterization  of Transfer,  Storage,  and
      Handling  of Waste  with  High  Emissions  Potential, Phase I.   Prepared
      for U.S.  EPA/ORD/HWERL.  Cincinnati, OH.  July  1985.   Appendix B.

66.   Spivey, J.  J.,  et  al.   Preliminary  Assessment of Hazardous Waste Pre-
      treatment  as an Air  Pollution  Control  Technique.   Prepared for U.S.
      Environmental  Protection Agency.  Publication No.  EPA  600/2-86-028!
      March  1986.  p. 333.

67.   ICF, Incorporated.   The RCRA Risk-Cost Model  Waste  Stream Data Base
      Prepared for U.S.  Environmental Protection  Agency,  Office of Solid
     Waste.  July 1984.

68.  Reference 67, p. 9.

69.  SCS Engineers.  Waste Characterization Data in Support of RCRA W-E-T
     Model and Regulatory Impact Analysis.  Prepared for U.S.  Environmental
     Protection Agency,  Office of Solid Waste.  July 15, 1983.
                                   C-90

-------
                                   TECHNICAL REPORT DATA
                            (Please read Instructions on the reverse before completing)
1. REPORT NO.
    EPA-450/3-89-023a
4. TITLE AND SUBTITLE
    Hazardous Waste TSDF - Background Information for
    Proposed RCRA Air Emission  Standards
    Volume I - Chapters 1-8,  &  Appendices A-C
7. AUTHOR(S)
            5. REPORT DATE
                 June  1991
            6. PERFORMING ORGANIZATION CODE
                                                            5. RECIPIENT'S ACCESSION NO.
            8. PERFORMING ORG/
9. PERFORMING ORGANIZATION NAME AND ADDRESS
    • Office of Air Quality Planning and Standards
     U.S. Environmental  Protection Agency
     Research Triangle Park,  North Carolina  27711
                                                            1C. PROGRAM ELEMENT
            11. CONTRACT/GRANT NO.

               68-02-4326
12. SPONSORING AGENCY NAME AND ADDRESS
     Office of Air  and Radiation
     U.S. Environmental Protection Agency
     Washington, B.C.  20460
            13. TYPE OF REPORT AND PERIOD COVERED
                Interim Final	
            14. SPONSORING AGENCY CODE

                   EPA/200/04
 15. SUPPLEMENTARY NOTES
 16. ABSTRACT

          Air emission standards are being  proposed under the Resource Conservation
     and Recovery Act for hazardous  waste treatment, storage, and disposal facilities
     (TSDF)  to reduce  emissions of ozone  precursors (volatile organic compounds) and
     exposures  to  hazardous  air  pollutants.    This document contains  background
     information and environmental and economic assessments of regulatory alternatives
     considered  in developing the proposed  standards.  The  regulatory alternatives
     consider application of  air  pollution controls  on  tanks,  surface  impoundments,
     and containers used to manage hazardous waste  at TSDFs, as well  as  at generators
     using tanks and containers to accumulate large quantities of waste on site.  This
     document is divided into a three volume  set.
                                 KEY WORDS AND DOCUMENT ANALYSIS
                   DESCRIPTORS
                                               b.lDENTIFIERS/OPEN ENDED TERMS
                                                                             COSATI Field/Group
      Air Pollution
      Volatile Organic Compounds
      Hazardous Waste
      Treatment
      Storage
      Disposal
    Air Pollution Control
13b
 18. DISTRIBUTION STATEMENT

      Unlimited
19. SECURITY CLASS (Til
    Unclassified
     346
                                                2O. SECURITY CLASS (This page/
                                                    Unclassified
                           22. PRICE
  EPA Form 2220-1 (R»v. 4-77)   PREVIOUS EDITION is OBSOLETE

-------

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











S
}~
UJ


g
'
i
M

P,
O

_J
C£
>—

g


CD

(/>
LU
cc
1^

o
_J
o

B
_i
n
L.

^1
<•£
J~l

z
1-
£

*
n
CO

Ul
_j
CO
£







ID






^f
JO
c
o
2
Q
0
O
U
49
c
o
o
CM







*H



























t.
O
o
o
V)





O (5) O) O






^ft O 0) 19





CO O O5 r4
IH





CO C5) 0) ^H
1-4






CO O 09 tH
1-4







O
C
a
O)
i_
o

O) T)
c c
•^ a
49
M C O
O "i- "c
3 CL a
•o ra
o « u
CL 49 C
o —
= ! „-
E «- —
o, a
^ i. .2
x a jc
00.0
•o C9* "a
c t- —
09 * -J3 49
C C — CO
— — C 3
c a i- -o
— L, 3 C
X O U. M





IS r*4 IS
ft IH





O iH (S
iH 1-1




«-l iH





19 fH O
1-1 t-l






O *H O
IH 1-1






CO
a
O

1
JC
o

•H
a
o

t>
1

-^ 10
.? 1
49 TJ
3 O
0 L.
o o.
•
n t. a
1. • O
1 "°-"|
««- - jc
— o
- a
n o -o
o — 0
.- TO 43
4» 0 f.
I) — O
• on
— — n





Oi rH






CO i—i





0> rt





O) «H







0) T^







—
•
o
o

•o
c
•

E
3
9

O
L,
49
0
Q.
£
49
O
3
TJ
O
1.
a
•o 01
0 O
— 49
* a
c
• •
L.
49 0
C JQ
— ja
a 3





tH CO IO JO IS U) IS






*H co m u) o u) o





rt CO 10 10 CM 10 0





iH CO LO 1O CM IO Q







•H (O IO tO CM tO 19















10
0

CL
Q.
3
0)
•0 49
X C C
fe - i
C X CL

JC 0 3
COCO"
8 .2 I 2 •
— « 49 0 C
c — a — a o
a a o a E —
r43 — o 43 to
0 «- — — a 43
X <*- O — O i
43 t- 0 U 0. 3
c a — — 49 G) <-
0 E a 0 o c 49
I — 49 C 0 a M
0 t. 0 O — t- C





^a} O






19 V"4





0 .-4





O <*4







o f~*



















O)
c n
'L, —
3 49
49 .-
O —
a *™

3 3
C
a m
E a
3 "D
| §
— t.
0 49
O O
a 0





O 5)






SI Q





S 5>





O O







Q O










ei
0

43
n —
0 to
— L.
a 0
co >
0 "c
a =
0 «T
o a
JC 43
CL
CO
.. o
m JE
•o
o -
TO JQ
• -
a o
t. t_
3 a
•o 0
C CO
^ &
0




c- to
(0





f** r*-
CO




r» co
CO





r*. co
CD





co
r- co













g)
L.
0

•o
c
a

4?
in
*
3
O
•o
u
a
N
a
JC
CO
a a
— 49
o o
i- 1-
o
43
in
a o


in in
3 43
o n 0
-o o 49
t. O CO
a a
N 43 *
a c
j= a co
43 3
/-v 10 O
•H C -O
^ o u
u a
43 N
a in a
jc a j=
43 J=
CO X M
C 49 3
o — a
.- — o
43—9
0. 0 CD
3  49
.2 8 x
0 49 —
— CO
js 9 a
aid.
49 9 a
o> o
— C 0




o

y^
X
c
a


^

1


4>
CO
JC
3

49
J3
3
O
9
CO 0

49 "a.

"~ 0

tT a
0 49

0 X
* —
O —
jc a
3
- 49
X O
— a
a -o
c —
'i o
0 *
c

0 0
in TJ
a o

u
0 0
0 JC

0 X
49 JO
13 T>
0 9
43 49
O O
0 —

X 0
£L
— 01
0
C L.
O 3
— CO
49 O
a —
t- O
C 9
0 JC
0) 49




— E
o a.
u a. •
49
C 5)
O (2
o to

C rH
O
— II
10
in *r  a
43 L.
C O CO
a c
CEO

'i CL 49
0 CL
T) S 0
9
U II —
CL O
IH U
"O ^-^ 43
9 C
to co o
a — o
-O O
1- 9
0 49 —
L. C CL.
a o E
o a
to x
t- 0
JS 0
O) 0
g -2 j5
20
j= >
49 0

r4 • *E
0 CL
CO > CL
C —
O <<- S
49 49 Q
O. O -
o 9 m
— «K II
2 2 u>
C T> TJ
o c c
u a a
_
                                                8-42