&EPA
United States
Environmental Protection
Agency
                       Office of Research and
                       Development
                       Washington DC 20460
Office of Solid Waste
and Emergency Response
Washington DC 20460
Technology Transfer
                       January 1989
EPA/625/6-89/019
Handbook

Guidance on Setting
Permit Conditions and
Reporting Trial Burn
Results

Volume II of the
Hazardous Waste
Incineration Guidance
Series

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                                       EPA/625/6-89/019
                                          January 1989
              Handbook


        Guidance on Setting
Permit Conditions and Reporting
          Trial Burn  Results

     Volume II of the Hazardous Waste
        Incineration Guidance Series
     Office of Solid Waste and Emergency Response
         U.S. Environmental Protection Agency
             Washington, DC 20460
        Risk Reduction Engineering Laboratory
                    and
     Center for Environmental Research Information
         Office of Research and Development
        U.S. Environmental Protection Agency
              Cincinnati, OH 45268

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                                        Notice
This document has  been  reviewed  in  accordance with  the U.S. Environmental Protection
Agency's peer and administrative review policies and approved for publication. Mention of trade
names or commercial products does not constitute endorsement or recommendation for use.

This guidance document is intended to provide information on how regulatory requirements in
40 CFR Subpart O may be satisfied in a wide variety of situations. This guidance document is
not,  in and of itself,  a regulatory requirement and  should not be regarded or used  as  such.
Therefore, although compliance with regulatory requirements is mandatory, compliance with this
guidance manual (although useful as a means of satisfying regulatory obligations) is  not.

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                                        Foreword
Today's rapidly developing and changing technologies and industrial products and practices
frequently  carry with them the increased generation  of  solid and  hazardous wastes.  These
wastes,  if not dealt with properly,  can threaten  both  public health and  the  environment.
Abandoned waste  sites and  accidental releases of toxic and hazardous substances to the
environment also  have important  environmental and  public  health  implications.  The Risk
Reduction  Engineering  Laboratory  assists  in  providing an authoritative and  defensible
engineering basis for assessing and solving these problems. Its products support the policies,
programs,  and regulations of the  Environmental  Protection Agency, the  permitting  and other
responsibilities of  State  and local governments, and the needs  of both  large  and small
businesses in handling their wastes responsibly and economically.

A recent study has indicated that two areas of guidance are needed to improve the permitting
process for hazardous waste  incinerators:

1.  Translation of trial burn results into permit conditions by the permit writer

2.  Reporting of trial burn data by the  permit applicant

The regional and state  permit writers  are charged with the responsibility to set specific permit
conditions  deemed  necessary to  safeguard public  health  and  protect  the environment.
Considering the complexity of incinerator systems and their operation and the variety of wastes
and trial burn cases, this task is clearly difficult. This  handbook  provides guidance to  the permit
writer on setting incinerator permit conditions.

Applicants  and their contractors now  report trial  burn test results  in a variety of formats. The
inconsistencies and deficiencies in the information and technical data provided in such reports
result in delays. A consistent format will assist the  applicant in drafting a complete and clear trial
burn report and facilitate the permit  writer's  review of the data.  This handbook suggests  a
format for trial burn reporting.

This document is Volume II of the  Hazardous Waste Incineration  Guidance Series.  The other
documents in this series are listed in Appendix A,  as  are sources of further guidance  relating to
hazardous waste incinerator permitting.
                                         E. Timothy Oppelt, Director
                                    Risk Reduction Engineering Laboratory
                                           in

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                                        Abstract
One of the most difficult and  time-demanding  tasks for a permit writer  is to evaluate and
interpret incinerator trial burn results and to draft facility-specific operating conditions based on
these results.  This handbook provides guidance to the permit applicant on reporting trial burn
data and to the permit writer on  translating these  data into meaningful and enforceable operating
conditions for incinerators.

This  report was submitted in  partial  fulfillment  pf  EPA  contract  68*03-3241  by the
Environmental Systems Division of Acurex  Corporation. Midwest  Research  Institute and the
Energy and Environmental Research Corporation participated as subcontractors. This work was
done under the joint sponsorship of the Office of Solid Waste and the Office of Research and
Development of the U.S. Environmental Protection Agency.
                                           IV

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                                       Executive Summary
 Introduction

 Subtitle C qf  the Resource  Conservation  and
 Recovery Act (RCRA) requires the EPA to develop,
 promulgate, and implement regulations which control
 the generation, the transportation,  and the treatment,
 storage, and  disposal (TSD)  of hazardous  waste.
 Regulations promulgated under RCRA at 40 CFR Part
 264,  Subpart  O, specify  the  following  performance
 standards,  which facilities treating hazardous  waste
 by incineration are required to meet:

 1,  99.99 percent destruction and  removal efficiency
    (ORE)  for each  principal  organic  hazardous
    constituent (POHC) in its permit for each  waste
    feed (or 99.9999 percent for dioxin listed wastes),

 2.  99 percent removal efficiency of HCI or 1.8 kg (4
    lb)/hr of HCI emissions, whichever is greater, and

 3.  Particulate  emissions  less than  180 mg/dscm
    (0.08 gr/cu ft), corrected to 7 percent oxygen.

 The regulations also require that fugitive emissions be
 controlled by  keeping  the combustion  zone totally
 sealed,  maintaining  negative draft, or an  equivalent
 alternative means of control.

 Facilities seeking a permit to incinerate  hazardous
 waste  are  required  to  demonstrate  the  unit's
 capability to meet the performance standards during  a
 trial burn.  Since incinerator compliance with  these
 performance standards cannot  be monitored over the
 long term,  the  conditions at  which  the incinerator
 operated during the trial  burn  (together with  any
 necessary  adjustments  to  those conditions)  are
 included in  the  incinerator permit  as conditions for
 continuing operation. Compliance with these operating
 conditions is then deemed to equal compliance with
the performance standards.  An  incinerator must be
 operated with a system to automatically cut off waste
feed to  the incinerator when operating conditions
 deviate from limits established in the permit.

Although the  regulations  specify four  operating
 parameters  that must  be set as  permit  conditions
based on the trial burn (carbon monoxide level, waste
feed rate, combustion temperature, and  an indicator
 of combustion gas  velocity),  it is  left to the permit
 writer to determine how to translate the trial burn data
 into permit conditions.  Because  of the  technical
 complexity of setting permit conditions for hazardous
 waste incinerators and  the flexibility the regulations
 allow in  setting  these conditions, there  has been a
 lack of consistency in  the operational  portions of
 incinerator permits issued across the country. Further,
 an  excessive  number  of permit  conditions  may
 severely  limit  flexibility  of  operation,  while  too  few
 permit  conditions  may  not provide  adequate
 assurance that the  performance  standards  will
 continue  to be met.

 Approach
 The major goals in developing the  guidance were to
 develop  a nationally  consistent,  technically sound
 approach  to the setting of operational conditions in
 incinerator permits  which would   maintain  proper
 performance while allowing a  reasonable  degree of
 operational flexibility. Technical rationales were to be
 stated in  the document so that it would also serve as
 a training  tool  and to  enable  the  permit  writer to
 identify and address cases where specific portions of
 the  guidance may  not apply.  Various  operating
 parameters thought to have an  effect on  achievement
 of  the incinerator performance  standards  were
 considered for inclusion in the guidance. "Back-up"
 parameters which  would  unnecessarily  limit  the
 permittee's flexibility to operate the incinerator were
 avoided.  The  conditions were  evaluated  based  on
 technical  knowledge,  and,  where  necessary,
 consensus of engineering judgment, to develop a set
 of operating  parameters  to be set  in  incinerator
 permits which would meet with the above goals.

Technical  and engineering guidance was provided by
 a panel of incineration  experts from  EPA Regional
Offices, the Office of Solid Waste,  and the Office of
 Research  and Development, and by representatives
of  the Research  Committee on  Industrial  and
 Municipal  Waste of  the American  Society  of
 Mechanical Engineers. In addition to providing experts
with whom the  authors  could discuss  ideas,  the
groups reviewed  two  successive drafts of  the
document.

 Description
The guidance document presents the  key control
parameters, shown in Table  1,  which  should  be

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 monitored during the trial burn and for which limits
 should be  set  in  the  incinerator   permit.  The
 parameters are divided into three groups.

 Group A parameters are continuously  monitored
 parameters  interlocked  to  automatic  waste feed
 cutoff. Most of these parameters are  based on trial
 burn conditions. A minimal amount of lag time may be
 incorporated into the limits for these  parameters by
 the use of averaging times following the guidelines in
 the document. Group B parameters are set to ensure
 that the "worst case" conditions demonstrated in the
 trial burn  are  not  exceeded during  continuing
 operation. These parameters  are  not linked  with
 automatic waste feed cutoff, and are not continuously
 monitored, but,  instead,  must be recorded  in the
 facility operating record. Group C parameters, which
 are set independently of trial burn results,  are based
 on  equipment manufacturers'  design  and operating
 specifications.  These parameters are not continuously
 monitored or linked to automatic waste  feed cutoff.

 Group A Parameters
 Temperature  is  a   key  parameter  of incinerator
 performance due to its influence on reaction kinetics
 and is a required incinerator  permit condition under
 RCRA regulations. The minimum temperature limit is
 generally set from the lowest  temperature trial burn
 test at  which  compliance   was  demonstrated.
 Combustion  chamber temperatures  are required by
 the regulations to be tied to  automatic waste feed
 cutoff. For  a  two-chamber  incinerator,  minimum
 temperatures would  be set for each chamber. When
 minimum temperatures are not  maintained in both the
 primary and secondary chambers, or in  the secondary
 chamber only,  waste feed must  be  cutoff to both
 chambers. However,  if only the primary chamber falls
 below  its  minimum  temperature, waste may still be
 fed to the secondary chamber.

 Carbon monoxide (CO) concentration in the stack gas
 is also a parameter  which  the regulations specifically
 require. CO is  used  as an indicator of  the  degree of
 mixing  achieved in the incinerator and  is related, by
 definition,  to   combustion  efficiency.   Separate
 guidance on setting  permit limits on CO to minimize
 emissions  of PIC's (products of incomplete
combustion) is  being prepared by EPA.

The hazardous waste incinerator regulations require
that the  permit  specify limits  for an indicator of
combustion gas velocity. Combustion gas velocity is
directly related to the gas residence time in  the
incinerator, which is known  to be one of the  key
parameters of  combustion. Residence  time becomes
more critical at lower combustion  temperatures. For
this reason,  the limit on  maximum combustion  gas
velocity should be based  on the maximum trial burn
 value measured during the lowest  temperature  test
 during which compliance was demonstrated.

 A waste  feed  rate limitation is required  by RCRA
 regulations primarily to minimize the potential loss of
 efficiency from overloading the combustion chambers.
 For  low  heating value wastes,  the  limits  are taken
 from the trial burn test with the minimum temperature
 during which  compliance was  achieved,  since  an
 increase  in the  waste  feed  rate  may  cause  a
 decrease in temperature.  Maximum  waste feed  rate
 for high  or medium heating value wastes are based
 on the highest feed rate  of these wastes from  any
 run.

 The requirement in  the regulations to control fugitive
 emissions is addressed by a permit requirement on
 the  operating pressure.  Incinerator chambers
 designed  to operate  under negative draft  (induced
 draft) are required by  the permit to maintain negative
 draft. Forced draft or positive  pressure incinerators
 must be  well  sealed, and  the  maximum  operating
 pressure is set based on the trial burn.

 The guidance  recommends that control parameters
 for air pollution control equipment (APCE)  be set to
 maintain  the particulate and acid scrubbing capability
 demonstrated during the trial burn. For  each type of
 APCE component, one key parameter was chosen to
 be tied   to the automatic  waste feed cutoff.  For
 example,  since the  principal  operating  parameter
 controlling  ESP collection  efficiency is the  power
 utilization, or  kVA, the minimum kVA demonstrated
 during the trial burn at the highest ash feed rate is set
 as the permit limit.

 Group B Parameters
 One of the key principles behind conducting a  trial
 burn is that the incinerator should operate under  the
 most severe conditions it is expected to  encounter for
 the duration of its  permitted  operation.  Group B
 parameters are included  in the guidance to ensure
that the  incinerator  will  not operate at more taxing
conditions  than those  at which it demonstrated
compliance during the  trial burn.

 Parameters affecting APCE performance included in
Group B are  total ash and chlorine loading  to  the
incinerator.   These  parameters   affect  the
concentrations  of  particulate and  HCI at the APCE
inlet and  the physical  and  chemical properties of  the
gas. The ash and  chlorine  loadings are  limited to  the
maximum rate  demonstrated in the trial  burn. A
minimum scrubber blowdown rate is also set based
on the trial burn,  since  suspended  and dissolved
solids in  recycle water,  which may  be re-entrained
into  the  flue  gas,  may  contribute to particulate
emissions.
                                                 VI

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  Table 1.
   Group
Control Parameters
                                  Parameter
  , Group A
  " Continuously monitored parameters are
   interlocked with the automatic waste feed
   cutoff. Interruption of waste feed is automatic
   when specified limits are exceeded. The
  .pararrieters.are applicable to all facilities.
   Group B
   Parameters do not_require continuous
   monitoring and are thus not interlocked with the
   waste feed cutoff systems. Operating records
   are required to ensure that trial burn worst-
   case conditions are not exceeded.
   Group C
   Limits on these parameters are set
   independently of trial burn test conditions.
   Instead, limits are based on equipment
   manufacturers' design and operating
   specifications and are thus considered good
   operating practices. Selected parameters do
   not require continuous monitoring and are not
   interlocked with the waste feed cutoff.
                               l.  Minimum temperature measured at each combustion chamber exit
                               2.  Maximum CO emissions measured at the stack or other appropriate location
                               3.  Maximum flue gas flowrate or velocity measured at the stack or other
                                  appropriate location
                               4.  Maximum pressure in PCC and SCC
                               5.  Maximum feed rate of each waste type to each combustion chamber1
                               6.  The following as applicable to the facility:
                                  • Minimum differential pressure across particulate venturi scrubber
                                  • Minimum liquid-to-gas ratio (L/G) and pH to wet scrubber
                                  • Minimum caustic feed to dry scrubber
                                  • Minimum kVA settings to ESP (wet/dry) and kV for ionized wet scrubber
                                    (IWS)
                                  • Minimum pressure differential across baghouse
                                  • Minimum liquid flowrate to IWS

                               7.  POHC incinerability limits
                               8.  Maximum total halides and ash feed rate to the incinerator system
                               9.  Maximum size of batches or containerized waste1
                             10.  Minimum particulate  scrubber blowdown or total solids content of the scrubber
                                  liquid

                             11.  Minimum/maximum nozzle pressure to scrubber
                             12.  Maximum total heat input capacity for each chamber
                             13.  Liquid injections chamber burner settings:
                                  • Maximum viscosity of pumped waste
                                  • Maximum burner turndown
                                  • Minimum atomization fluid pressure
                                  • Minimum waste heating value (only applicable when a given waste provides
                                    100% heat input to a given combustion chamber)
                             14.  APCE inlet gas temperature2
   11tems 5 and 9 are closely related; therefore, these are discussed under group A parameters.
   2ltem 14 can be a group B or C parameter. See text in Section 2.1.6.
The  Subpart  O regulations  require  that  POHC's
(Principal  Organic  Hazardous  Constituents)  be
designated for each  waste  feed.  The  required  ORE
must then  be demonstrated for  the POHC's during
the  trial  burn.  Since  the  POHC's  must  be
representative of the  waste feed,  they are chosen on
factors  such  as  difficulty  to   incinerate  and
concentration in the waste feed. The operator is then
limited  in the permit to burning only waste containing
hazardous constituents no more difficult to incinerate
than the  POHC's  for  which   compliance  was
demonstrated  during the  trial  burn.  The  heat of
combustion  of the  hazardous constituents  has  been
used to rank the incinerability of compounds  on the
premise  that  compounds  with  a  lower  heat  of
combustion  are  more  difficult to  burn. Field  data
indicate,  however,  that  other ranking  systems  may
exhibit  a better  correlation with  incinerability.  The
guidance presents a  draft  ranking  of the incinerability
of  Appendix  VIII  compounds  prepared  by   the
University of  Dayton  Research  Institute  based  on
thermal stability at low oxygen (TSLoOa) conditions.
A limit  on the maximum  size  of containerized  waste
fed to the incinerator is also recommended to prevent
oxygen depletion from  the sudden release of volatiles.
                                            The containerized  waste  fed  during the  trial  burn
                                            should  be  representative,  with  respect  to  volatile
                                            content, of the waste the facility will be burning under
                                            the permit.

                                            Group C Parameters
                                            Group C parameters  were formulated on the need to
                                            ensure that incinerator  operation  adheres  to  good
                                            combustion and APCE operating practices. To allow a
                                            reasonable  degree of flexibility  and  to  avoid  over-
                                            complication of  the  trial   burn,  limits  for  these
                                            parameters are based on manufacturer's design and
                                            operating specifications  rather than on the  trial burn
                                            settings.

                                            To  maintain proper atomization  of  liquid  waste and
                                            promote efficient  mixing,  burner settings  for liquid
                                            injection and afterburner chambers will  be limited to
                                            manufacturer's  specifications  or  other acceptable
                                            settings if data show that  they are adequate. These
                                            conditions   include  maximum  waste  viscosity,
                                            minimum atomization  fluid  pressure, and  maximum
                                            burner  turndown. The handbook  recommends that a
                                            minimum waste heating value be  set in the permit for
                                            liquid injection chambers where  100 percent of  the
                                            heat input  comes  from  the  waste feed.  Total heat
                                                      VII

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 input to the incinerator is limited to the incinerator
 design heat input capacity.

 The guidance recommends limiting  APCE inlet gas
 temperature due to its effect on  APCE performance
 as  well as  to prevent equipment deterioration.  The
 maximum inlet temperature to the APCE would be set
 at the trial burn value and a higher temperature would
 allow less condensation and thus render less of the
 particulate-forming material  subject to  collection.
 These  uncollected  gases  may then  condense
 downstream of the APCE as temperature decreases
 and form additional particulate matter. The maximum
 temperature  should  not be  higher  than  the
 manufacturer specification for maximum temperature.

 Other Permit Conditions
 The guidance  also  includes  additional  conditions
 related  to  waste feed cut off.  The  permit  should
 require  that minimum temperature be  maintained in
 the  secondary  combustion chamber  after a waste
 feed cutoff  until wastes remaining in the unit are
 burned  out. This heating  would  necessitate  use of
 auxiliary fuel but  must not conflict  with the unit's
 flame safety management system.  The guidance
 recommends a condition requiring quarterly reporting
 of automatic waste feed cut offs,  reasons for  the cut
 offs, and corrective actions taken.

 Translating Trial Burn  Results  into  Permit
 Conditions
 The guidance presents a strategy for  determining the
 limits on operating parameters and converting them
 into permit conditions. The goal in translating the trial
 burn results into permit conditions is to  ensure that
 the incinerator is operating in a  manner sufficiently
 similar to the successful  trial burn  conditions  to
 maintain  compliance  but still  allow  adequate
 operational  flexibility.  The  approach  commonly
 employed   is  patterned  after "mode-based"
 operation. The   permit contains  a different  set  of
 operating conditions for each waste combination the
 facility will burn. This  approach is best suited for a
 facility  dedicated to  treating  a well-defined  set  of
 uniform  composition hazardous wastes.

 The  above approach,  however,  is not  practical for
 facilities such as commercial facilities which  burn a
 wide variety of  wastes. The  guidance  presents an
 approach to developing a  single  set  of operating
 conditions (termed a "universal set of conditions" or
the "universal permitting strategy") which defines the
 allowable range  of operation  for  burning  all  of  the
 wastes in the facility permit. Under this approach, the
trial  burn must  attempt  to  achieve  worst-case
 conditions  for all permit parameters  at a  single
operating point by varying factors such as combustion
air flow and steam injection,  or  to  achieve  worst-
 case  conditions  in  multiple  tests with  the key
 operating parameters kept constant.

 In the general approach set forth in the guidance, the
 parameters are divided into three groups:

 1.  Control parameters set from trial burn data that
    are related to waste destruction
 2.  Control parameters set from trial burn data that
    are related to APCE performance

 3.  Control parameters that are independent of trial
    burn data

 Limits  on parameters are  set according  to the
 hierarchy above.  The groupings of these parameters
 are shown in Tables  2 through 4.  Permit limits must
 be set only from trial burn tests that show compliance
 with the performance standards. Limits should be set
 using  these  basic rules of thumb regarding "worst
 case"  conditions. The maximum  combustion gas
 velocity should  be   set from  the trial  burn  test
 conducted at the minimum temperature during which
 compliance was achieved. The maximum feed rate of
 each  low heating value  waste  stream  to  each
 combustion chamber should be that  demonstrated
 during the minimum  temperature test. The  maximum
 feed  rate  of  high heating value  wastes and the
 maximum combined feed  rate  should  be the
 maximums demonstrated at any point.

 Table 2. Waste-Destruction-Related Control Parameters
        Set from Trial Burn Data
 Type	Parameter	
  A    Minimum temperature at each combustion chamber exit
  A    Maximum CO emissions
  A    Maximum flue gas flowrate or velocity
  A    Maximum pressure in PCC and SCC
  A    Maximum feed rate of each waste type to each combustion
  B
chamber
Maximum size of batches of containerized waste
Permit  limits for APCE  parameters relating  to
particulate collection should be set from the trial burn
test at the maximum inorganic ash feed rate and the
maximum flue gas flow rate, because  ash  feed rate
determines the load to the APCE and an increase in
the flue gas  flow rate may  increase entrainment of
particulate matter. Minimum  liquor flow rate to the
absorber and minimum pH to the absorber should  be
set from the  trial burn test at the maximum total
halides feed rate and the maximum flue  gas flow rate.

In  some instances, it may not be possible to set the
conditions  in  the   manner  described   due  to
interrelationships  among  parameters which  prevent
certain conditions from being achieved at the  same
time. The guidance presents  an approach to estimate,
through calculations, whether the effect of setting the
                                                 VIII

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 Table 3. APCE-Performance-Related Control Parameters
        Set from Trial Burn Data
  Type	Parameter	
   A   Minimum differential pressure across paniculate venturi
       scrubber1
   A   Minimum L/G and pH to absorber1
   A   Minimum caustic feed to dry scrubber
   B   Minimum scrubber blowdown rates or maximum total solids in
       scrubber liquid1
   A   Minimum kVA settings to ESP (Wet/Dry) and kV for WS's1
   A   Minimum pressure differential across a FF1
   A   Scrubber nozzle pressure
   B   Maximum total halides and inorganic ash feed rate to the
       incinerator system
   B   Minimum particulate scrubber blowdown rate	

 1   Select as applicable to APCE system.
Table 4. Trial Burn-Independent Control Parameters
 Type	Parameter	
   C   Maximum total heat input for each chamber
   C   Liquid injection chamber burner settings
           •   Maximum viscosity of pumped waste
           •   Maximum burner turndown
           •   Minimum atomization fluid pressure
           •   Minimum waste heating value (if applicable)
   C   APCE inlet gas temperature	
presents a trial burn report format.  Example reporting
forms for the design, process,  and performance data
required in  a trial  burn report  have been developed
and are presented  in the document.

Summary
The  Guidance  on Setting  Permit Conditions and
Reporting Trial  Burn Results has been developed to
assist permit writers  in translating trial burn  results
into  site-specific  operational  conditions  in  an
incinerator permit. These parameters are presented in
the document along with guidance on how to develop
permit operating conditions using the trial burn data.

The guidance  will  also assist applicants in  planning
trial burns to address  the key operating parameters
that must be measured and  emphasize the necessity
to test "worst-case" operations to  enable applicants
to tailor their proposed operating  conditions  to  the
needs of their facility. One of the key points  made by
the guidance is that the permit writer  and  applicant
should agree, prior to  the trial  burn,  on what  permit
conditions will result from the trial burn as planned. In
this way, it can be determined whether it is necessary
to make  modifications to the  plan to  obtain the
desired operating conditions.
conditions based on less than  worst-case runs  will
be  significant.  For example,  if the permit  limit for  the
maximum flue gas velocity is to be set from a data
point other than the minimum temperature test,  the
permit writer would calculate whether  it is likely that
the flue gas  flow rate at the minimum temperature
could be increased to the maximum flue gas flow rate
without  causing  ORE  to decrease  belpw  99.99
percent. This is done by relating flue gas  flow rate to
residence time to  ORE  assuming  a  first-order
reaction.

The guidance emphasizes the importance of planning
the trial burn to obtain the desired permit conditions.
The applicant and permit writer should  agree, prior to
the trial burn, on the permit conditions that will result
from the trial  burn as planned, assuming  compliance
is demonstrated. This will allow the applicant to make
modifications to the  trial  burn plan,  if necessary,  to
obtain the desired operating conditions.

Trial Burn Reporting
The permit writer  is  often faced  with reviewing a trial
burn  report  which is incomplete or  which  is  not
structured  such  that the  information  necessary  to
evaluate compliance and set permit conditions can be
readily located in the report. The permit  writer may
need to  go  back   to  the  applicant  to  request
clarification or additional data, which slows down the
review process. To assist both applicants and permit
writers,  the guidance describes the information  which
should  be  included in the trial burn  report and
                                                    IX

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                                             Contents
 Chapter
Page
 Foreword 	   iii
 Abstract  	   iv
 Executive Summary	   v
 Figures  	   xiv
 Tables	   xv
 List of Terms	   xvii
 Conversion Factors  	   xix
 Acknowledgments   	   xxi

 1   Introduction  	   1
    1.1  RCRA Regulations  	   1
    1.2  Incinerator  Permitting Requirements  	   2
        1.2.1   New Facilities	   2
        1.2.2  Existing Incinerators   	   4
    1.3  Evaluating a Trial Burn and Establishing Permit Conditions  	   4

 2   Control Parameters	   9
    2.1  Group A Parameters	   10
        2.1.1   Temperature  	   11
              Mechanics of POHC Destruction	   12
              Determining Temperature Limit	   12
        2.1.2  CO Emissions 	   14
        2.1.3  Gas  Velocity Indication   	   14
        2.1.4  Combustion Chamber Draft or Pressure   	   15
        2.1.5  Maximum Waste Feed Rate	   17
        2.1.6  Air Pollution Control Equipment	   18
              Acid  Gas Formation and Control  	   18
              Particulate Formation and Control  	   20
    2.2  Group B Parameters  	   22
        2.2.1   POHC Selection and Incinerability Ranking  	   22
        2.2.2  Maximum Halides and Ash 	   23
        2.2.3  Maximum Batch and Container Size  	   24
        2.2.4  Minimum Particulate Scrubber Slowdown   	   24
    2.3  Group C Parameters  	   25
        2.3.1   Burner Settings 	   25
        2.3.2  Total Heat Input  	   25
        2.3.3  APCE Inlet Gas Temperature  	   25
    2.4  Other Parameters	  .   26
    2.5  References	   27
3   Setting Permit Conditions  	   29
    3.1  Permitting Approach	   29
    3.2 Interrelating Control Parameters  	   31
    3.3 Treatment of Variations in  Data   	   31
                                                 XI

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                                      Contents (continued)


    3.4 Single Point Approach	32
    3.5 Multiple Point Approach	 . .	   32
    3.6 Universal Approach	   33
       3.6.1  Control Parameters Related to Waste Destruction	   34
       3.6-2  Control Parameters Related to APCE Performance	 ;	   37
       3.6.3  Control Parameters Independent of Trial Burn Data	   39
    3.7 Determining Operating Envelope	   39

4   Example Test Case  	   41
    4.1 Site Description  	   41
    4.2 Structuring of the Trial Burn	'.	   41
       4.2.1  Waste Selection and Feed Rates	   42
       4.2.2  Trial Burn Operating Conditions		   45
       4.2.3  Operating Conditions: APCE		   46
    4.3 Trial Burn Test Results   	   46
    4.4 Determining Limits on Control Parameters	   46
       4.4.1  Control Parameters Related to Waste Destruction	   51
       4.4.2  APCE-Related Parameters	  . 54
       4.4.3  Parameters Independent of Trial Burn Data	 .	   55
       4.4.4  Summary of Operating Limits	   55

5   Data Reporting	 .   59
    5.1 Design Data Reporting	   59
    5.2 Trial Burn Result Reporting	 . .	 .	   60
       5.2.1  Suggested Report Format	   64
       5.2.2  Guidance for Reporting Process and
                 Continuous Emissions Monitor (GEM) Data  	   71
             Reporting Continuously Monitored Parameters	   72
             Special Problems	   73
             Processing and Reporting CO Data	   74
    5.3 Operational Recordkeeping and  Reporting	   74
    5.4 Available Computer Program Support	   75
       Hazardous Waste Control Technology Data Base	   75
       Energy and Mass Balance Calculation	, .	   75
    5.5 Recommended Forms for Presenting Data Summaries	   75

6   Inspection and Maintenance Guidelines	   79
    6.1 General Facility  Equipment	   79
    6.2 Safety and Waste Cutoff Interlocks	'   81

Appendix A:  Sources of Further Information  	   83

Appendix B:  Guidance for Incinerator Design  Review	   85
    B.1 Overall Facility Design	   85
    B.2 Incineration Equipment  	   86
       B.2.1  Liquid Injection  Incinerators   	   87
       B.2.2  Rotary Kiln Incinerators	   88
             Waste Devolatilization	   89
             Ash Retention Time	   89
             Particulate Entrainment	   89
       B.2.3  Multiple Hearth  Incinerators	   89
       B.2.4  Fluidized  Bed Incinerators  	   90
    B,3 Temperature and Gas Residence Time  	   90
       B.3.1  Calculation Technique  	   90
                                                XII

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                                     Contents (continued)


       B.3.2 Example Test Case	   92
    B.4 Air Pollution Control Equipment  	   95
       B.4.1 Wet Systems	   97
             Quench Chambers	   97
             Packed-Bed Scrubbers	   98
             Venturi Scrubbers	   98
       B.4.2 Dry Systems	    100
             Mechanical Collectors  	    100
             Electrostatic Precipitators  	    100
             Fabric Filters	 > . .    100
             Spray Drying Absorbers	 . .	    100
    B.5 Measurement Techniques and Safety Interlocks   	    101
    B.6 Special Wastes and Similar Systems	    101
    B.7 References	    101

Appendix C:  Time and Temperature Dependency of the Destruction Process  	    103

Appendix D:  Designating Principal Organic Hazardous Constituents   . <	,	    105
    D.1 Background	    105
    D.2 Construction of the Ranking	    106
    D.3 Using the Ranking	    106
    D.4 References	    107
Appendix E:  Energy  and Mass Balance Computer Program	    125
    E.1 Energy and Mass Balance	    125
       E.1.1  Input	    125
       E.1.2 Mass Balance	    127
       E.1.3 Energy  Balance	 . . .	    128
       E.1.4 Residence Time	  .	    131
       E.1.5 Units in Series   	    132
       E.1.6 APCE	    132
       E.1.7 Limitations of the Current Procedure	 ..,	    132
    E.2 References		    132

Appendix F:   Example Reporting Forms	    135
Appendix G:  Example Reporting Forms: Filled out for Data
                from Example Problem	    159
                                               XIII

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                                              Figures


Number                                                                              Page

1-1    Incinerator permitting process - new facilities	   3
1-2    Incinerator permitting process - existing facilities (interim status).   . . ;		   5
1 -3    Steps to evaluating trial burn plan and establish permit conditions	   7
2-1    Example of a temperature trace	    14
2-2    Effluent flow versus air flow for combustion	• • •    16
2-3    Effect of pressure drop on venturi scrubber efficiency	 .    21
4-1    Incinerator system for example test case.   .	    42
4-2    Operating envelope for example test case.	    57
5-1    Example process diagram showing  monitoring points.	    66
5-2    Example of process diagram showing sampling locations.	    70
5-3    Example of trial burn test timeline.	    74
B-1    Incinerator equipment arrangements	    86
B-2    Actual-to-ideal residence time ratio
          versus moisture-to-air mass flow ratio.		    91
B-3    Ideal temperature versus total heat  input
          to total mass input ratio and fractional heat loss	    93
B-4    Correction to ideal temperature versus
          ideal temperature and waste/total mass flow ratio	    94
B-5    Difference between higher and lower heat value versus
           combustion water parameter and moisture in wet fuel/waste.   . . .  .	    94
B-6    Combustion water parameter versus mass fraction
          H in dry fuel/waste and mass fraction Cl in dry fuel/waste.  . .	    94
B-7    Schematic of incinerator for energy and mass balance example	    97
B-8    Typical APCE schematic (wet system)	    98
G-1    Strip Chart Recording of Combustion Temperatures - Run 1-1	   196
G-2    Plot of Corrected  CO Readings from Data Logger 1-min Averages - Run 1-1     	   197
                                                XIV

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                                              Tables


Number                                                                              Page

1-1    Contents of Trial Burn Plan	   2
2-1    Control Parameters  	   11
2-2    Recommended Waste Feed Cutoffs  	   12
2-3    Limits on Chamber Draft or Pressure	   17
3-1    Permitting Approaches  	   30
3-2    Waste-Destruction-Related Control Parameters Set From Trial Burn Data     	   31
3-3    APCE-Performance-Related Control Parameters Set From Trial Burn Data    	   32
3-4    Trial Burn Independent Control Parameters   	   32
4-1    Example  Incinerator Test Case: Summary Design Information 	   43
4-2    Example  Incinerator Test Case: Major Physical and Chemical
           Characteristics of Onsite-Generated Wastes    	   44
4-3    Example  Incinerator Test Case: Trial Burn Test Matrix (Target Settings)	   46
4-4    Example  Incinerator Test Case: Summary of
           Process Operation Results - Test Condition 1   	   47
4-5    Example  Incinerator Test Case: Summary of
         .Process Operation Results - Test Condition 2   	   48
4-6    Example  Incinerator Test Case: Summary of
           Process Operation Results - Test Condition 3   	   49
4-7    Example  Incinerator Test Case: Summary of
           Emission Performance Results - Test Condition 1  	   50
4-8    Example  Incinerator Test Case: Summary of
           Emission Performance Results - Test Condition 2  	   50
4-9    Example  Incinerator Test Case: Summary of
           Emission Performance Results - Test Condition 3	   51
4-10   Average Trial Burn Results at Three Test Conditions	   52
4-11   Summary of Permit Limits  for Incinerator Example Test Case  	   53
4-12   Data Used for Setting Temperature Limit  	   53
5-1    Trial Burn Reporting Format and Requirements - Main Report   	   61
5-2    Trial Burn Reporting Format and Requirements - Appended Information  	   64
5-3    Example Summary Table of Process Monitors  	   67
5-4    Example Summary Table of Sampling and Analysis Methods  	   68
5-5    Process and GEM Data Requirements   	   71
5-6    Recommended Usage of Sample Forms in Trial Burn Report  	   76
6-1    Recommended Inspection  and Maintenance Frequency  	   80
6-2    General Maintenance  and Troubleshooting of Incinerator and Auxiliary Equipment	   80
6-3    General Maintenance  and Troubleshooting of Air Pollution Control Equipment  	   81

B-1    Incineration Equipment  	   88
B-2    Input Data for Energy  and Mass Balance Example  	   96
B-3    Comparison of EER Energy and Mass Balance Results with
           Permit Application Design Calculations  	   97
B-4    Typical Values of Kga  	   99
D-1    Principal Hazardous Organic Constituent Thermal Stability Index  	   109
D-2    Principal Hazardous Organic Constituent Thermal Stability Index -
           Alphabetized Version   	   116
                                                xv

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                                     Tables (continued)


Number                                                                           Page

D-3    Appendix VIII Thermal Stability Classes  	   123
E-1    Energy and Mass Balance Input Data  	   126
E-2    Molecular Weights of Species Considered in Energy and Mass Balance  	   128
E-3    Molar Equations for Complete Combustion  	   128
E-4    Weighted Gray Gas Constants  	   131
F-1    Recommended Usage of Sample Forms in Trial Burn Report   	   136
G-1    Response to APCE Parameters, Form 6 "Summary of Test Results" 	   179
G-2    Response to APCE Parameters, Addendum to Form 5  	   187
G-3    CombustionTemperature Data Taken from Strip Chart - Run 1   .	  200
G-4    CEM Data from Data Logger Files - Run 1-1  	  202
                                             XVI

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                                   List of Terms
ACFM     Actual cubic feet per minute
APCE     Air pollution control equipment
CE        Combustion efficiency
                                   C02
                                         * 100 (percent)
                                co2+co
CEM       Continuous emission monitor
CO        Carbon monoxide, compound from partial oxidation of hydrocarbons
DE        Destruction efficiency of the combustor (only)
                       POHC. -POHC .     ,  t.   ,   ,
                 __        in        out combustion chamber  . „_ ,
                 DE= -      - *100 (percent)
DOE      Department of Energy
ORE      Destruction and removal efficiency of the incinerator (including APCE)
                            POHC. -POHC  „ ._-_
                                                    *100 ("ercent)
                                          .n

EERC     Energy and Environmental Research Corporation (Irvine, California, Telephone (714)
          859-8851)
EPA      United States Environmental Protection Agency
ESD      Environmental Systems Division of Acurex Corporation (Mountain View, California,
          Telephone  (415) 961-5700)
ESP      Electrostatic precipitator
FF        Fabric Filter
HCI       Hydrochloric acid emissions regulated under RCRA to 1 percent of organic chlorine
          feed or 1.8 kg (4 lb)/hr maximum emission rate
HHV      Higher heating value
HWCTDB  Hazardous Waste Control Technology Data Base at ORNL
                                        XVII

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                               List of Terms (continued)

   ID        Induced draft
   I&M       Inspection and maintenance
   IWS       Ionizing wet scrubber
   kVA       kilovolt-amperes
   L/G       Liquid-to-gas  ratio
   LHV       Lower heating value
   MM5      EPA Modified Method 5 Paniculate Stack Test Procedure
   MRI       Midwest Research Institute (Kansas  City, Missouri, Telephone (816)  753-7600)
   NPDES    National Pollutant Discharge Elimination System                    • ..   . ,
   ORNL     Oak Ridge National Laboratory
   PCC       Primary combustion chamber
   PIC       Products of incomplete combustions
   POHC     Principal Organic Hazardous Constituent
   QA/QC    Quality Assurance/Quality Control
   RCRA     Resource Conservation and Recovery Act of 1976 and Amendments
   RREL     Risk Reduction Engineering Laboratory, USEPA, Cincinnati, Ohio
   SCC       Secondary combustion chamber
   SCFM     Standard cubic feet per minute
   TSD       Treatment, Storage, and Disposal
   TSLoO2    Thermal stability at low or deficient oxygen level
   TSHiO2    Thermal stability at high or oxygen rich level
   TUHC     Total unburned hydrocarbon
   UDRI      University of Dayton Research Institute
   VOST     Volatile organic sampling train
aFor this document, PIC refers to RCRA Appendix VIII organic compounds (100 ppm) not present in the feed
that results from combustion of waste.
bRCRA Appendix VIII organic compounds selected for evaluation of ORE during trial burn.
                                           XVIII

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                                        Conversion Factors
        Multiply
 atmospheres (pressure)
 centigrade (C)

 centimeter (cm)
 centipoise (cP)
 cubic centimeter (cm3)
 cubic meter (m3)

 cubic meter/second (m3/s)
 gram (g)

 gram/(centimeter»second) (g/[cm»s])
 gram/cubic centimeter (g/cm3)
 gram/cubic meter (g/m3)
 gram/liter (g/L)

 gram/milliliter (g/mL)
 inch of water @4°C
 (in H2O @ 4°C)

 kilogram (kg)
 kilogram/minute (kg/min)
 kilojoule (kJ)
 kilojoule/kilogram (kJ/kg)
 kilojoule/second (kJ/s)
liter (L)
 liter/cubic meter (L/m3)
meter (m)
pascal (Pa) (kPa = 103Pa)

pascal»seconds (Pa»s)
  By
101.3
°F = (1.8 x °C) + 32
°K = °C + 273.17
0.254
0.01
0.061
35.31
1.31
1,000
2119
0.001
0.0022
1
62.427961
0.437
1,000
0.0624
1
0.0025
0.0361
2.205
132.3
0.9478
0.43
3,412
0.035
7.48
3.281
9.869233 X 1Q-6
10
10.00
             To Get
 kilopascal O(kPa)
 Fahrenheit (F)
 Kelvin (K)
 inch (in)
 gram/(centimeter*second) [g/(cm»s)J
 cubic inch  (in3)
 cubic foot (ft3)
 cubic yard  (yd3)
 liter (L)
 cubic feet per minute (cfm)
 kilogram (kg)
 pound (Ib)
 poise (P)
 pound/cubic foot (Ib/cu ft)
 grain/cubic foot (gr/cu ft)
 part/million (ppm)
 pound/cubic foot (Ib/cu ft)
 gram/cubic centimeter (g/cm3)

 atmosphere (atm)
 pound/square inch (psi)
 pound
 pound/hour (Ib/hr)
 British thermal unit (Btu)
 British thermal unit/lb (Btu/lb)
 British thermal unit/hour (Btu/hr)
 cubic foot (cu ft)
gallon/1000 cubic feet (gal/1,000 cu ft)
foot (ft)
atmosphere (standard) (atm)
 dyne/square centimeter (dyne/cm2)
poise
                                                  XIX

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       Multiply
poise (P)
square meter (rr»2)

stoke (St)
ton (metric)
 By

100.00
1
1
0.0672

10.76
1x102
1
3.875
0.001076

1,000
1.1023113
                            To Get

               centipoise (cP)
               dyne*second/square centimeter
               gram/(centimeter»second) (g/[cm«s])
               pdund/(second«foot) [lb/s«ft]

               square foot (sq ft)

               centistoke (cSt)
               square centimeter/second (cm2/s)
               square foot/hour (ft2/h)
               square foot/second  (ft2/s)

               kilogram (kg)
               ton (short 2,000 Ib mass)
xx

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                                Acknowledgments
This guidance document was prepared for the U.S. Envfrbnmental Protection Agency's (EPA's)
Office of Solid Waste and the Office of Research and Development under the overall direction
of Sonya Stelmack and C.  C.  Lee. The document  was prepared by Acurex  Corporation's
Environmental Systems Division with contributions by the Midwest Research Institute (MRI), and
the Energy and Environmental Research Corporation (EERC).

Principal Investigator: Leo Weitzman (Acurex)

Assistant Investigators: Andy Murphy and Carlo Castaldini (Acurex)

Technical contributions were also made by Robin Anderson (EPA), Donald Oberacker (EPA),
Wyman  Clark  (EERC), Gary  Hinshaw (MRI),  Scott  Klamm (MRI),  Randall Seeker (EERC),
Andrew  Trenholm (MRI), Barry Dellinger (University of Dayton Research Institute).

Additional technical contributions and review were provided by a panel of incineration experts
from selected EPA Regional Offices. This panel included Gary Gross of Region  III, Betty Willis
of Region IV, Y. J. Kim of Region V, and John Hart of Region  IX.

Drafts of this document were  also reviewed  by  the Incinerator Permit Writers' Work Group of
the EPA and by the Research Committee on Industrial and  Municipal Waste of the American
Society of Mechanical Engineers, as well as Joseph J. Santoleri of Four Nines, Inc.
                                                                                                     1
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                                                                                                     j
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                                         XXI

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                                            CHAPTER 1
                                           Introduction
When  an owner  or operator of  a hazardous waste
incinerator is issued a permit, conditions are specified
that must  be  satisfied  during  operation. These
conditions include limits on operating  parameters
such  as temperature, gas  residence time, and CO
emissions that are chosen  to ensure that legal and
safety  standards are met. The limits are chosen by
analysis of  the results  of  a  "trial  burn"  that
demonstrates the performance of the incinerator.  This
handbook provides guidance on using trial burn  data
to set realistic and  enforceable  permit  conditions.
Conversely,  the  guidance in this handbook can be
used to  design a trial burn for  an incinerator.  The
handbook also  provides  suggested  formats for
presentation of trial burn data.

This chapter describes the  impact of the trial burn
and the data it generates on the permitting process.
This is not a comprehensive review of the regulations
and permitting  procedures but  is a summary to
provide background for the reader.

1.1 RCRA Regulations
The Resource Conservation  and Recovery  Act
(RCRA)  requires the  Environmental   Protection
Agency (EPA) to  establish  regulations governing the
handling  of hazardous wastes. Regulations governing
incineration of  hazardous  waste   wer'e  first
promulgated on January  23, 1981,  and  have since
been amended  numerous times. These  regulations,
codified in 40 CFR Part 264, Subpart 0 and Part 265,
Subpart O, are part of EPA's comprehensive set of
regulations  that prescribe design and performance
standards for hazardous  waste  production, storage,
transport, disposal, and treatment. A permit program
that is used to administer the regulations.

The RCRA  regulations  cover  a  wide  variety of
facilities.  They  set  standards for generators  and
transporters of hazardous wastes  and for  owners and
operators of  treatment and disposal facilities.  The
general permit requirements for all treatment, storage,
and disposal  (TSD) facilities  are described in
Standards  for   Owners  of  Hazardous  Waste
Treatment, Storage,  and Disposal Facilities, 40 CFR
264. These regulations require that an owner or
operator satisfy requirements such as to:

•  Develop  a contingency plan  and  emergency
   procedures
•  Maintain extensive records
•  Develop a closure and post-closure plan
•  Meet financial requirements
•  Manage containers, tanks, surface impoundments,
   waste piles, and landfills properly

The permit regulations  governing  hazardous waste
incinerators are covered in 40 CFR 264, Subpart  0,
which  requires that  the  owners  or  operators  also
perform the following:

•  Analyze wastes as specified in the permit

•  Meet the following performance standards:
   -  99.99 percent destruction and removal efficiency
     (DRE)  of selected  principal organic hazardous
     constituents (POHCs) and 99.9999 percent DRE
     for dioxin listed wastes
   -  99 percent removal of hydrochloric acid (HCI) or
     1.8 kg  (4 lb)/hr HCI  emissions, whichever  is
     greater
   -  180  mg/dscm (0.08  gr/cu  ft)  of  particulate
     emissions (corrected to 7 percent 62)

•  Operate the incinerator  according to operating
   conditions specified in the permit for the following:

   -  Carbon monoxide (CO) level in exhaust
   -  Waste feed rate and composition
   -  Combustion temperature
   -  Indicator of combustion gas velocity
   -  Allowable variations in design
   -  Other  requirements  necessary to  meet
     performance standards

•  Control  fugitive emissions
•  Install automatic waste feed cutoff

•  Perform inspections and monitoring (I&M)
•  Remove all hazardous waste and hazardous waste
   residues upon closure

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Although  not  addressed  herein,   upcoming
amendments  to  the  incinerator  regulations  may
include:
• Changes in the requirements for carbon  monoxide
   (CO) emissions
• Risk-based limits on metals emissions
• Risk-based verification of HCI emissions
• Lower particulate emission limits based on the best
   demonstrated available technology

1.2 Incinerator Permitting Requirements
The  RCRA regulations  require  all  owners  and
operators of TSD facilities  to  obtain an  operating
permit from the  appropriate regulatory  agency:  the
EPA  Regional  Office  or,  if authority has  been so
transferred,  a  State agency. To obtain a permit,  the
applicant submits the following information:

• Description of the facility
• Security procedures and inspection schedule
• Contingency plan
• Description of preventive maintenance  procedures
• Description of the waste
• Personnel training program
• Plan and cost estimates for closure
• Assurance  that the  operator  of  the  facility  is
   financially responsible

The permitting process  for an  incinerator  usually
includes a "trial burn," which is a test to determine
whether  the  unit  can  meet  the  performance
requirements specified by the regulations. Although it
is possible to  satisfy this requirement by submitting
information showing that a trial burn  is not required,
this is a rare occurrence that will not be discussed
here. As  part of the  permitting process for a  new
incinerator, the owner or operator is required to obtain
prior approval of a trial burn plan from the regulatory
authority.  Table  1-1 lists  the major information  that
must be included in a trial burn plan.

Table 1-1.   Contents of Trial Burn Plan
   Analysis of waste(s)
   Quality Assurance/Quality Control (QA/QC) Plan
   Engineering description of facility
   Sampling and monitoring procedures
   Test schedule
   Test protocol (operating conditions)
   Emissions control operating conditions
   Shutdown procedures
   Other necessary information
There are different procedures for permitting new and
existing  hazardous  waste  incinerators.  Existing
incinerators are those that have been operating under
 interim status.  These  incinerators  receive  a RCRA
 permit after the trial burn. The trial burn plan does not
 require prior  approval from  the  permitting  agency,
 although this is highly recommended.

 The   other  permitting  procedure  is  for  new
 incinerators.  Because  these  are  not allowed to be
 constructed or  to operate without a permit, they are
 permitted prior to construction. Typically, the permit
 allows them to operate for a limited period of  time
 after  construction and  prior to the test burn  to allow
 time for startup and  shakedown.

 1.2.1 New Facilities
 Rgure 1-1 outlines  the major steps in the  permitting
 of new facilities. First, the permit application including
 the trial burn plan (or in rare cases, data in lieu of the
 trial burn) is  submitted to the permitting  authority.
 Then the application goes  through  an  administrative
 review to ensure that  the  application and test  plan
 include all the major  components  required by  the
 regulation.  After this review,  the application  is
 evaluated to  determine  whether  all the  technical'
 information required is  provided and if it is  internally
 consistent. It  is important to  note that even though
 the regulations  provide for  a  two-step administrative
 and technical  review process, many offices combine
 these  steps  and do  not  consider  the  application
 complete  until it  contains  all  the  information
 necessary to issue the draft permit.

 The permit writer then  makes a determination about
 the likelihood that the facility will achieve compliance
 with the  RCRA regulations  and that its operation will
 not be a hazard to  public health or  the environment.
 This procedure is complex,  and the permit writer  may
 seek assistance from a number of the manuals listed
 in Appendix A.  At this point,  a tentative decision is
 made  to issue or deny the permit.  This decision is
 followed  by public notice,  a public  comment period,
 and final  issuance or denial of  the permit.

 After  the  permit is  granted, the facility  is  built  and
 operated under the  startup/shakedown  provisions of
 the regulations.  The  permit will include restrictions on
 operation  during this period. This  "pretrial burn"
 period may last up to 720 operating hours (defined as
 hours of  operation while hazardous waste are burned
 rather than  elapsed  time  or  time  when  only
 nonhazardous  fuels are burned) and may be extended
 for an additional 720 hours of  operation. It is followed
 by the trial burn.

 Following  the  trial burn, the  facility  operates under
 conditions  set  by the  Director (the EPA  Regional
Administrator  or  State Director  for  States with
 permitting authority) until the  trial burn  results  are
 submitted and evaluated. The evaluation  is  designed
to answer the following two questions:

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     Figure 1-1.   Incinerator permitting process - new facilities.
CO
        Permit application
                                                         Technical evaluation
                                                         period
                                                         •    Design
                                                         •    Operation
                                                         •    Waste
                                                              characterization
                                                              Trial burn plan
Deficiencies
•   Completeness
•   Accuracy
•   QA/QC
           IsRCR
          compliance
           probable?
Information
complete?
Public
comment
period
                                                                                                                                         Issue draft permit for
                                                                                                                                         •   Pretrial bum
                                                                                                                                             period
                                                                                                                                             Trial burn
                                                                                                                                             Posttrial bum
                                                                                                                                             period
                                                                                                                                             Long-term
                                                                                                                                             operation
                                                             Pretrial
                                                           bum period
                                                Public
                                                comment
                                                period
 Issue/
 deny
permit?
                                                        Construction
                                                          of facility
                                        period (trial burn
                                        data evaluation)

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•  Under what operating  conditions (if any) did the
   facility satisfy the RCRA requirements?

•  Are the conditions  in the permit adequate, or must
   they be modified to  reflect the results of the trial
   burn?

Assuming that  the trial  burn  was  successful, the
permit conditions are modified, if necessary, and the
facility proceeds to operate.

1.2.2 Existing Incinerators
The permitting procedure for existing incinerators, i.e.,
those  operating under interim  status, is  shown in
Figure 1-2. As  can be seen, the procedure is similar
to that for new incinerators. The principal difference is
that because the facility is already operating prior to
being issued a permit, it does not need one for either
startup and shakedown or for  the  trial burn]  As a
result, the decision to approve or deny the permit is
deferred until after the trial burn results  have  been
submitted and  evaluated. Once again,  the  simplified
flow diagram (Figure  1-2) should not  be interpreted
to mean that the public comments  cannot alter this
issue/deny decision for the permit.
                              " "&— -.  " ' •  . •
The sections above  describe the permitting process
in general terms. Regulations in 40 CFR Part 270 and
in Part 284, Subpart  O, should be consulted for full
information.

1.3 Evaluating  a  Trial   Burn  Plan   and
Establishing Permit  Conditions
Sections  1.2.1  and  1.2.2 briefly described  the
permitting  process  for  both  existing   and  new
incinerators. They  identified the point where the trial
burn fits into the overall permitting procedure and the
points  where the permit writer must  evaluate the trial
burn  information. The  remainder of this,  handbook
gives guidance  on  assessing the trial  burn plan (if
prior agency approval is sought or required) and the
trial  burn  results and on  establishing  the  operating
conditions specified in the permit that is issued for the
facility;  they  are  referred   to as  the  "permit
conditions."

Figure 1-3 illustrates  steps 1-3 that are followed in
evaluating the trial burn plan and in establishing the
permit conditions relating to the  plan. Figure 1-3 also
illustrates  steps 4-6  that  are followed  after  the trial
burn  to set permit  conditions.., After  the  permit
application is received and found to be complete and
technically acceptable, the trial burn plan is reviewed.
The evaluation  process described here is for a new
incinerator; however, because the procedure for new
and existing units is  virtually identical except for the
point  in the process where the  permit  is  actually
written (before the trial burn for a new incinerator and
after the trial burn for  an existing one),  the  remainder
 of  this  handbook will  not  differentiate  these two
 permitting Scenarios further.
    <     '      ; '. .  •      '       > :••.
 Step  1  in  evaluating  the trial  burn  plan  involves
 selection of the  appropriate design  and  operating
 parameters (referred to as  control parameters) that
 form  the basis of the permit. During  this evaluation,
 the permit writer  and the applicant should agree  on
 the following:                          .

 • Key incinerator operating parametersv
 • The parameters for which limits will be specified in
   the permit
 • The effect  of  the  trial burn on  establishing  these
   limits                              •
                          *;       ;'

 Prior  to  finalizing the trial burn plan,  agreement  on
 these points between the  applicant and permit  writer
 is very important  and highly recommended. In  many
 cases, operational difficulties can  be  minimized and
 regulatory compliance  can  be  achieved  by proper
 design of a plan agreed to  by the two parties.

 Step  2  in' evaluating  the  trial burri plan  involves a
 Comparison  of   the  incinerator  system  design
 parameter^  and the control  parameters.  This review
 examines ,the' doijitrdl  parameters  for both  internal
 consistency and1  for  consistency with  the design
 parameters. This review also determines whether the
 operation of this system is likely to comply with the
 pertinent regulations and, more importantly, if the test
 is likely  to  result in an imminent  hazard to public
 health or the environment.

 Jp step 3 of the trial plan evaluation  process, limits are
 set on the contrbl  parameters consistent with the step
 2 reyiew. These  limits  are included.in the  permit as
 conditions, the', permit conditions,  that -define the
 range of acceptable operation  for: the incineration
;system for the four phases of operation applicable  to
 a new incinerator:               \           ;^     '-
 • Startup/shakedown
 • Trial burn
 • Post-trial burn
 » Continuing operation

 The  permit  conditions also  include monitoring and
 automatic cutoff requirements on some ofkthe control
 parameters. The mbnitofirtg conditions  are included  to
 validate   compliance  and  facilitate  enforcement
 activities.

 this handbook does not deal specifically with the trial
 burn   except  for a  discussion  of the  format
 recommended  for presenting the results.  The reader
 is referred  to the  appropriate manuals  listed  in
 Appendix A for further guidance on this subject.
 During the  trial  burn,  the control  parameters are
 measured,  and  the  values are  recorded in  an

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         Figure 1-2.   Incinerator permitting process - existing facilities (interim status).
           Permit application
                                                            Technical evaluation
                                                            period
                                                            •   Performance
                                                            •   Operation
                                                            •   Waste
                                                                 characterization
eficiencies
   Completeness
   Accuracy
   QA/QC
Information
complete?
 Is trial
  burn
required?
en
Yes

	
Notice of
intent to
deny permit

,
                                                                                                                           No
 ;    Review   j
 ;    trial bum  j
>j      plan
                                                                                                                                       No
                                                        —I            /•  V
                                               !   Modify   j         /      \
                                               ' trial burn  \A No   ./'  Is trial   \
                                               !    plan    *     «x  burn OK? /
                                                                                                                           Yes
                                                                                                                            	  Dashed lines indicate optional steps.
                                                                                                  ;JHI

-------
"operating  log."  This  log is as  important as  the
emission and pollutant release data  and  must  be
included in the trial burn report. It is submitted along
with the  results  of the  trial burn  to  the permitting
agency.

In step 4, the permit writer compares the values of
the control parameters with  the  measured  levels of
emissions,  effluents,  and  wastes produced by  the
incinerator  during the  trial burn. The intent of  this
evaluation is to verify that the limits set in step 3 do,
indeed, result in compliance with the  regulations  and
with safe and environmentally acceptable operation. If
necessary,  the limits on the control  parameters are
adjusted at this point to reflect  the results of the  trial
burn.

Step 5 of the permitting process is  setting the permit
conditions for the incinerator. The permitting strategy
for  the incinerator is designed to organize the  limits
on  the  control  parameters into  a  consistent,
enforceable set of permit conditions. See Sections
3.4, 3.5, and  3.6 for methods that can be  used to
develop the strategy.

The final step, step 6, in this process is specification
of the I&M requirements in the permit as required by
40  CFR 264.347. These requirements  can  include
operational, safety, and  other hardware that does not
directly  relate to the  trial  burn  and  the  permit
conditions  developed from  it. The I&M conditions
discussed  here  emphasize  those  requirements  that
relate  to  the  control  parameters.   Other  I&M
procedures, i.e.,  those  put on  the thermocouples,
pressure sensors, alarms, and circuitry  that monitor
the  control parameters  and trigger actions such as
waste  feed cutoffs  are outside  the  scope  of  this
handbook.                    .

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Figure 1-3.   Steps to evaluating trial burn plan and establishing permit conditions.
Trial burn plan
Design
Operating conditions
Estimated emissions
Estimated waste
Other

	 k
Step 1
Select control parameters
• Design parameters
• Operating parameters
— Temperature
- CO
- Gas flow rate
- Pressure
- Etc.


Step 2
Review of
Design
Operating conditions
Etc.
or consistency with
Design parameters
Operating parameters
and likely compliance with
Regulations
Safety & environmental
factors
— 	 1

Step 3
Set appropriate permit
conditions
• Operation
• Monitoring
• Performance
• Etc.
Trial bum report
Design

Measured emissions
Measured waste
Other






Step 4
Evaluate values of
• Control parameters
• Emissions
• Effluents
• Wastes
•i» Etc.

k



Steps
Determine permitting
strategy
• Single point
* Multiple point
• Universal
• Set operating envelope





Step 6
Specify inspection and
maintenance requirements
• Equipment 1 & M
• Alarms
• Emergency cutoffs


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                                            CHAPTER 2

                                        Control Parameters
 Incinerator  operating  conditions  are  defined by
 "control parameters" such as temperature, pressure,
 waste  feed rates,  and limits on  halogens  in  the
 wastes,  which  can be  reliably  measured  during
 incinerator operation. Control  parameters  are
 important  because performance parameters such as
 ORE and particulate emissions cannot be directly and
 continuously measured during actual operation. As a
 result,  limits are placed on  the control parameters,
 i.e., ranges are set for measurable parameters, and
 these limits are set as conditions in the final operating
 permit.  The ranges of acceptable conditions  are
 determined from  the  trial  burn.  As  long  as  the
 incinerator is  operated within these  ranges,  it is
 assumed to be operating under the same conditions
 as during  the successful trial burn and, hence, to be
 in compliance with the regulations.  It is  necessary,
 therefore,  to select the control parameters before the
 trial burn and to  measure their values throughout the
 trial burn so that the results may be used to set their
 limits.

 This chapter recommends the control parameters that
 should be used and explains  the reasons they were
 chosen. Note  that it is assumed that the reader is
 familiar  with the construction and  operation  of  the
 common types of  incinerator systems  and  ancillary
 equipment. See Appendix B for  a  discussion of
 incinerator designs and guidance on reviewing them
 during the permitting process.

 Control  parameters fall  under the  following  two
 classifications:

 1. System  Parameters, defined as  basic  design
  specifications  that typically are  fixed  for a  given
  incinerator or incinerator configuration

 2. Operating  Parameters,  defined  as  easily
  changeable  parameters  that  control the  day-to-
  day performance of the incinerator
 The system parameters are  functions  of the design
and construction of the  incineration  system  and
 normally cannot  be changed once the  incinerator is
built. They include such items as:
 •  Size and  shape  of  the  primary  combustion
   chamber  (PCC)  and  secondary  combustion
   chamber (SCC)
 •  System configuration
 •  Size of pipes and ducts
 •  Capacity of the fans and pumps
 •  Location and type of monitoring equipment
 •  Type and configuration of the air pollution  control
   equipment (APCE)
 •  Dimensions of components such  as  feed  chute,
   auger, and screw feeder for solids handling

 Generally, system  parameters are incorporated into
 the permit by reference to  design drawings and
 specifications  and  are not directly  discussed  further
 here.  Operating parameters are easily  changed  to
 accommodate fluctuations  in  the  demand  on the
 system and other constantly changing factors. These
 parameters include  the following:

 •  Temperatures at various points in the PCC, SCC,
   APCE, stack, etc.
 •  Pressure  at various points  in  the  system and
   pressure drops  across key pieces of equipment
   within the system
 •  Carbon monoxide (CO) and 02 concentrations at a
   selected CO monitoring point
 •  Gas flowrates in  the system
 •  Waste and primary fuel feed rates
 •  Waste composition such as ash, moisture, volatile
   content, and halogen content
 •  Excess combustion air into PCC and SCC
 •  Burner atomization setting
 •  APCE-related parameters,  i.e.,  pressure   drop,
   scrubbing liquor flowrate, pH, and plate voltage

 To establish  meaningful  and  enforceable  permit
 conditions  and   to  avoid  mutually   exclusive
 requirements,  the  operating parameters  should  be
considered in relation to each  other and in relation  to
the system parameters. A goal of this handbook is to

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 avoid setting redundant parameters, where consistent
 with technical judgement and regulatory requirements;
 however,  it  is  important to  be  aware  of  the
 interactions between the various  permit  conditions
 and ensure that they are internally consistent. For
 example,  for  some facilities,  a  limit  on  minimum
 temperature and maximum gas throughput would also
 define the minimum and maximum thermal duties
 (total heat input),  waste feed  rate, and excess 02-
 Since  the  regulations  require that at least some of
 these  other parameters be  regulated, it is important
 that  they be  internally  consistent.   Wherever
 technically  possible  and  consistent  with  the
 regulations, it should be  the permit writer's  goal to
 eliminate redundant restrictions.

 The remainder of  this chapter discusses the control
 parameters and selection of their  limits.  Table 2-1
 lists the  control   parameters  pertinent  to most
 incinerator facilities. As can be seen, they  have  been
 grouped  into three categories identified as groups A
 through C. This nomenclature is  somewhat arbitrary
 and was  chosen  simply to  clarify  the ensuing
 discussions.

 Group A parameters are  based  strictly on trial  burn
 results and  require  continuous  monitoring  and
 automatic waste feed  cutoff when  permit limits are
 exceeded. Because these may  fluctuate  rapidly
 during normal operation,  short-term  deviations  from
 the  acceptable range may be  tolerated.  These
 variations are discussed further in Section 2.1.

 Group B  and  C  parameters are  not  continuously
 monitored and, consequently, are not interlocked with
 automatic waste feed  cutoff. The primary difference
 between  groups B  and C is that  operating limits for
 group  B  parameters also are  based strictly on trial
 burn results,  whereas  limits  for group C  parameters
 are based on equipment design specifications and do
 not necessarily reflect operational  settings recorded
 during  the trial burn.

 The only requirement for group C parameters is that
 the operating conditions recommended do not deviate
 from those specified by the  equipment manufacturer
 and  are  compatible with  good operating  practices.
 This treatment of group C parameters allows greater
flexibility  in  the permit  because  worst-case
 operational settings  for these parameters are  not
 investigated during the trial burn  to  demonstrate
compliance with a desired envelope. This  procedure
formally and legally requires that the operator use the
 equipment in the manner and under the conditions for
 which  it  was  designed.  For example, nozzles  will
typically be designed to properly atomize a liquid or
 slurry of specified ranges of viscosity, vapor pressure,
 etc. The nozzles will not perform  well if these ranges
are  exceeded,  and incinerator performance  may
deteriorate. Permit conditions that require adherence
 to  manufacturer specifications  thus  ensure  good
 operating practices.

 The issue has been raised that, in some cases, there
 are  no  manufacturer's specifications  because  the
 equipment may  have  been made by the  applicant or
 custom built for  this application. Also, in some cases,
 the applicant may find that the equipment works well
 outside  the  specified ranges.  In that  case,  the
 applicant should provide design specifications and,  if
 the  reviewer requests,  backup material  on  the
 adequacy of the specifications and of the  equipment.
 It may be necessary to  incorporate testing of  the
 proposed ranges for  these parameters into the trial
 burn. If the trial burn shows the incinerator to perform
 properly  when  the  equipment in  question  operates
 well outside  the manufacturer's  or  design speci-
 fications, the  permit  limits  may be set at  the
 demonstrated levels.

 Note that a waste feed cutoff  is not the same as an
 incinerator shutdown.  In a cutoff,  the incinerator may
 keep operating on auxiliary fuel and on  nonhazardous
 waste  until the problem is corrected; and, except in
 extreme  situations,  continued  operation is  desirable
 so that furnace  temperature is maintained. A control
 parameter such  as  temperature  that  exceeds
 specification triggers a waste feed cutoff,  not a total
 shutdown of the  system.

 A final word of caution regarding the type of systems
 used for the  waste feed cutoffs.  The systems  must
 be fully automatic to  satisfy the requirements of  the
 regulation. A  meter  or strip-chart  output that  is
 periodically checked by an operator who shuts off  the
 waste feed if a problem is  noticed is not an adequate
 substitute for  an automatic system.  An  automatic
 system must monitor  the  parameter  and  initiate  the
 waste feed shutoff when an excursion is  detected. It
 is highly  desirable that the system  also  trigger  an
 alarm as the parameter approaches the cutoff limit to
 allow for  corrective action.

 The  following  sections explain the  reasons these
 parameters were selected. The discussion  provides
 insight on the selection and interdependence of the
 control  parameters.  It also  suggests  alternative
 approaches that  may  be more appropriate in special
cases.  The section closes  with a discussion  of those
 parameters which were considered for  inclusion but
were  not selected along with  the rationales  for
excluding these  parameters  and a discussion  of
 situations when they should be  considered.

 2.1 Group A Parameters

There are six "group A parameters":
 1. Temperature  of  the gas  at  each  combustion
  chamber exit
2. CO emissions
                                                 10

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 Table 2-1.
  Group
Control Parameters
                                             Parameter
  Group A
  Continuously monitored parameters are interlocked with the
  automatic waste feed cutoff. Interruption of waste feed is
  automatic when specified limits are exceeded. The
  parameters are applicable to all facilities.
  Group B
  Parameters do ngt/equire continuous monitoring and are thus
  not interlocked with the waste feed cutoff systems. Operating
  records are nevertheless required to ensure that trial burn
  worst-case conditions are not exceeded.

  Group C
  Limits on these parameters are set independently  of trial-
  burn test conditions. Instead, limits are based on equipment
  manufacturers' design and operating specifications and are
  thus considered good operating practices. Selected
  parameters do not require continuous monitoring and are not
  interlocked with the waste feed cutoff.
                                          1.  Minimum temperature measured at each combustion chamber exit
                                          2.  Maximum CO emissions measured at the stack or other appropriate
                                             location
                                          3.  Maximum flue gas flowrate or velocity measured at the stack or other
                                             appropriate location
                                          4.  Maximum pressure in PCC and SCC
                                          5.  Maximum feed rate of each waste type to each combustion
                                             chamber1
                                          6.  The following as applicable to the facility:
                                             • Minimum differential pressure across paniculate venturi scrubber
                                             • Minimum liquid-to-gas ratio and pH to wet scrubber
                                             • Minimum caustic feed to dry scrubber
                                             • Minimum kVA settings to ESP (wet/dry) and kV for ionized wet
                                               scrubber (IWS)
                                             • Minimum pressure differential across baghouse
                                             • Minimum liquid flowrate to IWS

                                          7.  POHC incinerability limits
                                          8.  Maximum total halides and ash feed rate to the incinerator system
                                          9.  Maximum size of batches or containerized waste1
                                         10.  Minimum particulate scrubber blowdown or total solids content of the
                                             scrubber liquid

                                         11.  Minimum/maximum nozzle pressure to scrubber
                                         12.  Maximum total heat input capacity for each chamber
                                         13.  Liquid injections chamber burner settings:
                                             • Maximum viscosity of pumped waste
                                             • Maximum burner turndown
                                             • Minimum atomization fluid pressure
                                             • Minimum waste heating value (only applicable when a given waste
                                               provide 100% heat input to a given combustion chamber)
                                         14.   APCE inlet gas temperature2
  11tems 5 and 9 are closely related; therefore these are discussed under group A parameters.
  2 Item 14 can be a group B or C parameter. See text in Section 2.1.6.
3. Indicator  of combustion  gas  velocity (flue gas
   flowrate)
4. Maximum waste feed rate
5. Pressure in the PCC
6. APCE

The  regulations  (40  CFR 264.345(a))  specifically
require that the levels of the first four parameters  be
set in the permit based on the trial burn results. They
also allow additional conditions to be set as deemed
necessary by the permit writer.  In addition,  40 CFR
264.347  requires continuous monitoring  of  the first
four  parameters.  It is  recommended   that  those
parameters for which  the permit  sets conditions  but
does not require continuous  monitoring  be logged at
least every  15 min.  The following  sections discuss
each of  the  parameters  and  setting conditions  for
them.

2.7.7 Temperature
The  regulations  require  that suitable  interlocks  be
provided  to shut off the hazardous waste feed  if  the
temperature  drops below  a value  specified in  the
                                              permit (see  40 CFR 264.345(f)).  This section  gives
                                              guidance on establishing the minimum temperature in
                                              each  combustion chamber  which will  trigger  the
                                              automatic waste feed cutoff.

                                              A minimum temperature must  be specified for each
                                              chamber of an incinerator.  It is recommended that the
                                              temperature at which the  waste feed is cut  off be
                                              specified  as   not  less  than  the  lowest  mean
                                              temperature  at which a successful test (minimum of
                                              three runs) occurred. If this level is not appropriate for
                                              a facility, a rolling average temperature limit similar to
                                              that  which  will  be used for  CO  emissions  is
                                              acceptable. When these  limits are  established,  it is
                                              important that the minimum temperatures for both the
                                              PCC and SCC be determined from the same test. As
                                              discussed  in the  example  given in Chapter 4,  it is
                                              possible  for  the  SCC  to achieve  its  minimum
                                              temperature during  one test while the PCC achieves
                                              its minimum during another.

                                              It is not necessary to cut off all waste feeds when the
                                              temperature  in only  one chamber  drops  below  the
                                                      11

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 minimum. Table 2-2 summarizes the  recommended
 guidelines for specifying this.
Table 2-2.   Recommended Waste Feed Cutoffs

                             Waste Feed Is Cut Off To:
Gas Temperature Below
Minimum In:
 SCC only
 PCC only
 SCC and PCC
                            Both PCC and SCC
                            PCC only
                            Both PCC and SCC
  PCC = Primary combustion chamber.
  SCC = Secondary combustion chamber.
As shown, hazardous waste feed to both chambers
should  be stopped if the temperature in  the SCC
drops  below  the  trigger value.  If  only the PCC
temperature  drops  below the trigger  value, the
hazardous waste feed to the SCC may continue, and
only the hazardous waste feed to the PCC needs to
be stopped.

The rationale for waste feed  cutoff to both chambers
when the  gas temperature in the SCC drops below
the minimum is that the gas leaving the PCC may still
contain undestroyed POHCs  and hazardous products
of incomplete combustion (PICs).  These compounds
may not be destroyed if the SCC is not maintaining
an adequate temperature. Continued operation of the
SCC if the temperature in the PCC  drops below the
minimum  is  necessary  since  the  waste   usually
contributes energy to maintain the SCC temperature.
Sudden changes  in the  SCC fuel feeds should  be
avoided when there are problems  with the PCC that
may be releasing  POHCs or PICs.  As long  as the
SCC temperature is being maintained, waste  feed to
it may  continue.

In performing this evaluation,  the permit  writer is
cautioned  to consider the  location and placement of
the temperature sensor. These factors are especially
critical  when  upset conditions  are being monitored;
for example, during the extreme case of "flameout" in
the SCC.  The temperature  of the  bulk gas  in the
chamber would quickly  drop;  however, the  walls,
which have a very high thermal mass, would  remain
hot  for a  long time.  If  improperly installed,  the
temperature sensor would absorb heat by radiation
from the walls and indicate a higher temperature than
that  to which the  residual  POHCs are actually being
exposed.   See the  Engineering   Handbook  of
Hazardous Waste Incineration,  (1) SW-889, and
Hazardous  Waste   Incineration  Measurement
Guidance  Manual  (2) for more information  on this
subject.

The  remainder of this section discusses the effects of
temperature,  gives additional information to  explain
 the  above recommendations,  and  shows  how  the
 temperature limits are calculated from test data.

 Mechanics of POHC Destruction
 Destruction of a POHC is a multistep process. First,
 the compound is vaporized either in a solids handling
 system such  as a rotary kiln, hearth, or fluidized bed
 or, if  a liquid, by  a nozzle.  Then,  the  vaporized
 materials are exposed to a flame  where the majority
 of the POHCs are destroyed. A small fraction of the
 POHCs that typically escape the flame zone requires
 an extended  residence time (~1  sec) at elevated
 temperatures [~1,000°C (1,830°F)] to be destroyed.

 The time/temperature dependence  of the destruction
 process is described in Appendix  C.  Generally,  the
 longer the residence time and the higher the chamber
 gas  temperature,  the greater the destruction of  the
 POHC fraction that escapes the flame; the different
 segments  of the  complex flow  patterns in  the
 combustion chamber will have different temperatures.
 The area  immediately around the flame  will be very
 hot and poor in oxygen. As the gases  move away
 from  the  flame, they  mix  with  additional  oxygen
 (secondary air),  but their temperatures  drop.  Along
 the walls,  the refractory will be relatively cool, and  it
 will keep the adjacent gases cool.
 The degree of POHC destruction that will be achieved
 in any one slug  of  material  that passes through  the
 combustion  chamber  will  be  a  function of the
 time/temperature (and  oxygen)  regime that the
 particular slug is exposed to as it follows a somewhat
 random path  through the  chamber. The  majority of
 the slugs of gas that contain POHCs will pass through
 the flame  and be  destroyed,  A  small  percentage,
 however, will  bypass the flame  and  follow a path
 which  typically results in  a lower  level of  POHC
 destruction. This complexity does  not lend itself to
 detailed analysis without a  major investment in time
 and testing that is beyond the permitting  process in
 all but special cases. Fortunately,  the  trial burn data
 preclude the need for a detailed temperature profile of
 the incinerator.

 Determining  Temperature Limit
 As discussed above, the temperature at which waste
 must be cut off to the incinerator is determined from
 the trial burn. This subsection discusses how such a
determination  can   be  made and  gives additional
 rationale to support the decision.

According  to  EPA policy for trial  burns,  three runs
 must be conducted  at  each temperature  although a
 larger number of replicates may performed to provide
 insurance against loss of data from  any one run. The
 minimum operating temperature for the incinerator is
defined as the lowest temperature at which a set of
 runs was performed during  the trial burn.  If a test is
conducted at  only one temperature, that temperature
 is defined as the minimum.
                                                12

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During  each test, the replicate  runs are performed
under as similar  conditions as practical; however, a
slight variation in the mean temperature  is common.
The mean temperature used to  set  the  minimum  is
the  average  of  the  mean  temperatures  of  the
replicate runs constituting the test.

The permit condition for  the  minimum operating
temperature is the  lowest mean  temperature that
resulted in a successful test. The automatic interlock
should  be  set  so  that  the waste  feed  to  the
appropriate chamber is cut off when  the  temperature
drops below this value.

It is recognized that  this is a somewhat conservative
automatic waste  cutoff level.  If the incinerator  is
operated at the lowest mean temperature at all times,
frequent cutoffs are likely. The operator can avoid the
cut-off trips by operating the  incinerator  at a slightly
higher temperature than this minimum. Thus, the trial
burn would  be performed  at a  temperature slightly
lower than that desired for operation.

The second method  that can be  used is  to base the
waste feed cut off on an hourly rolling average of the
temperature  during  operation.  The hourly rolling
average has been defined as the mean of the  60
most recent  1-min  values  measured  by the
continuous monitoring system. For calculation of each
hourly  rolling average  value,  the new data point  is
added to those taken over the specified  time period
and  the least recent  data point is excluded from the
average. The permit condition then would specify that
waste feed  should be  cut off when either (1)  the
temperature drops below  a minimum (which is  the
lowest temperature measured during the trial burn ) or
(2)  the  rolling 60 minute  average temperature falls
below the mean determined from the trial burn. The
absolute  minimum  temperature for waste  cutoff,
condition (1) above, should be the lowest temperature
from the trial burn.   Its purpose  is to trigger an
immediate waste  feed  shutoff in case of a  sudden,
catastrophic temperature decrease.

T.ne  following  example  illustrates the  function and
intent of  the lower  temperature limit. Consider an
incinerator whose secondary chamber's temperature
is  being  maintained with a  high  heating  value
hazardous waste. Assume, further, that  because  of
improper  blending, water  has accumulated  in the
waste storage  tank  and the  feed  system  begins
sending this water instead of the combustible waste
to  the  high  heating  value waste burner. The  flame
would become very unstable and the temperature in
the  SCC would drop  rapidly;  however,  the
temperature sensor  would  continue  to average the
drop in  temperature  with the  values  from the paste
hour of  operation and not trigger waste feed cutoffs,
or alarms, for several minutes. A secondary cutoff at
a low temperature would eliminate this problem. It is
recognized that the flame instability described above
 would most likely trigger a waste feed cutoff because
 of CO limits; however, these are also based on a
 rolling average and could, conceivably, also result in a
 delay.

 In order to  assure  that normal  fluctuations  in the
 temperature  do  not trigger waste feed cutoffs, the
 lower  temperature  should  be  set  at  the  absolute
 lowest (not  the mean) temperature encountered
 during  the trial  burn. This is essential  since the
 purpose of requiring the added complexity  of a rolling
 average temperature would be defeated if normal
 variations in  the temperature  could  trigger  a waste
 feed cutoff.

 For  example, Table  F-15  of  Appendix F lists the
 SCC and PCC temperatures for each minute during a
 trial  burn.  The  "sampling  time"  for  these  data is,
 therefore, 1  min. The rolling average of the SCC and
 PCC temperatures for the first 60 min is the mean of
 each set  of  temperatures  recorded between 1,250
 and  1,309 min. At  1,251  min, the rolling  average
 becomes the mean of that  calculated between 1,251
 and  1,310 min. This pattern is continued for each new
 interval.

 A rolling average  type of  permit condition  requires
 that  the temperature  monitoring  system  include, a
 computer  capable of calculating the rolling  average
 continuously. Because of the added complexity* the
 rolling  average conditions should only be used when
 requested by the applicant.

 The  remainder  of  this section  gives  background
 information  to  support  the two approaches for
 establishing the waste feed  cutoff level and describes
 methods for  calculating the mean temperature  and
 the other values needed to set the permit conditions
 on temperature.

 The  temperature limits recommended can  usually pe
 readily specified.  The trial burn  report normally
 includes copies  of the temperature  monitor outputs
 and a summary of the mean, maximum, and minimum
 values for  each run.  The  temperature  of: an
 incinerator  is  always monitored continuously  by at
 least a strip-chart recorder and  usually a data  logger
 that  also records  the  temperature  at  30-sec to 1-
 min  intervals. The  time-weighted  average is'the
 arithmetic  mean of  the temperatures recorded at
these intervals. If a mean is not given in the report,- it
 can be calculated from the  temperature log (if given)
 or the  strip-chart  recorder  output by  the following
 method.

 Figure 2-1  is an example  of  a strip-chart  recprder
output. Because  fluctuating data usually have a rough
 periodicity,  a  visual  examination  will identify  some
 minimum period  to  the fluctuation. A period  smaller
than this minimum is  selected as the sampling rate.
 For example,  if  the  fluctuations vary at  a 1- to 3-
min  rate, the 1-min rate is used.  Then,  the strip-
                                                 13

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Figure 2-1   Example of a temperature trace.
    CD
    D.

    
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 measure  parameters which can  be  related  to the
 combustion gas  flowrate.  Upper limits need  to  be
 placed on  combustion gas flow/rates for the following
 three  reasons.  The first  is  to  control  the gas
 residence  time in each chamber.  The second is to
 control the gas throughput throughout the system to
 minimize  back  pressure  at joints  and seals; for
 example, at the inlet of a rotary kiln to the SCC. The
 third is. to control the gas flowrate through the APCE
 to ensure that it is not overloaded.

 Note that while the measurement of "an indicator of
 gas velocity" is required by the RCRA regulations (or
 more correctly, they require that limits be placed on
 this parameter), it is not an independent variable. The
 flue  gas flowrate is  interrelated  with  the  pressure
 measurements described  in subsequent sections.
 Limits on gas  flowrate cannot be set without affecting
 the limits on pressure parameters in the incinerator.

 This section  is  not  intended  to provide detailed
 guidance on the  type of flue gas  measuring  device
 that should be used.  See the Engineering Handbook
 for Hazardous Waste Incineration  (1),  SW-889, and
 the  Hazardous  Waste  Incinerator  Measurement
 Guidance  Manual  (2)  for such  guidance.   Some
 advice is  given  below  on the placement  of  such
 monitors.

 The  combustion  gas flowrate can  be monitored  in
 several different ways. The preferred  method  is the
 use of a direct gas flow  monitor at the outlet  of the
 SCC. In some systems,  however, conditions such as
 high temperature, high particulate  loading, and high
 acid gas loading could result in unsatisfactory life and
 performance of the monitor.

 Another option, and often the more practical one, is to
 place the monitor just before the stack. Although this
 practice increases the likelihood of introducing  errors
 due to air infiltration or changes in  the water content
 of the gas  stream, which can be difficult to predict, it
 results in an increased life and performance reliability
 for the monitor. If this  site  is  chosen  for the
 combustion gas monitor, the permit writer should add
 constraints on the water  content and permissible air
 infiltration  upstream  of  the monitor  to maintain
 conditions consistent with those achieved during the
trial burn.

When neither of these alternatives is practical,  it may
 be possible to measure the combustion air flowrate
 instead of the  combustion  gas. For a  given
temperature, the flowrate of the combustion gas (the
products of combustion) can be approximated  within
reasonable accuracy  by the  flowrate of the
combustion  air, i.e.,  the  primary and  secondary air
being fed  to  the combustor.  In  most cases, the
combustion air constitutes 95 percent or more of the
combustion gas,  as illustrated by Figure 2-2,  which
 shows the consistency of this correlation for different
 conditions. In many cases, especially for forced-draft
 incinerators,  the  primary and secondary combustion
 air can be measured fairly  easily.  When this is  the
 case, to monitor  combustion air is a good alternative
 to monitoring combustion gas.

 Another method  of  measuring  the  combustion gas
 flowrate is to monitor the power usage (voltage and
 current are adequate, in most cases) of the induced
 draft fans, although sufficient technical justification in
 the form  of actual power usage versus gas flowrate
 should  be given to document its accuracy in a given
 system.

 The limits on the flue gas velocity set by the  permit
 conditions  should  be  based on the  maximum
 combustion  gas flowrate that was  measured  during
 the trial burn. This  flowrate  measurement should be
 taken at the  minimum observed temperatures  during
 the test to  ensure that the condition  includes  the
 lowest temperature  and shortest residence time that
 achieved acceptable incinerator performance.

 2.1.4 Combust/on Chamber Draft or Pressure
 The draft or  pressure in  the chambers   of  an
 incinerator is  regulated  to minimize the release  of
 partially burned POHCs  and  other untreated products
 of combustion as fugitive emissions from the  PCC.
 Fugitive emissions  are regulated  under  40 CFR
 264.345(d).  These  emissions  are of concern  in
 multichamber  and especially in rotary  kiln systems
 that partially  degrade  the   wastes  into  gaseous
 components  in the  PCC and  feed the off-gases
 containing large amounts of POHCs, PICs, acids, and
 particulates, first  into the SCC where the PICs and
 POHCs are destroyed and, then, into the air pollution
 control  devices where the pollutants are removed to
 below  the required level.  The release of  these
 intermediate gases is normally prevented by  setting
 limits on the  maximum pressure at which the  PCCs
and SCCs can operate.

Normally, the gases from the PCC are forced into the
SCC by the pressure differential between the  two. If
there is a  sudden increase in the gas production rate
in the PCC or a draft decrease in the SCC that may
be  caused by a fan failure  or an  increase   in the
burning rate,  partially burned  POHCs  and PICs  as
well as  particulate and acid  gases from the primary
chamber can be released. Increases in  the pressure
in the PCC can be caused by an explosion or when a
drum of exceptionally flammable  waste ignites. Any
condition that  results in  the  sudden release of more
gas than the  upstream system can  accept will result
in an overpressure. Normally, the system between the
PCC and SCC is equipped with seals that can contain
the gas from  a specified level of overpressure.  When
this level is exceeded, however, untreated gases are
released.
                                                 15

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        20,000
         17,500
     I
     uJ   10,000
                   Adiabatic temperature = 2,000°F
                   Chamber volume = 1,000 ft3
Ideal case: pure air
Combustion with pure monochlorobenzene
Combustion with 10% monochlorobenzene in soil
Combustion with 50% monochlorobenzene in water
Combustion with 25% monochlorobenzene in water
                                 20,000
  Figure  2-2.   Effluent flow versus air flow for combustion.
                                    40,000

                                  Airflow (Ib/h)
60,000
80,000
The fugitive  emissions problem is most common  in
rotary  kiln incinerators where the  kiln must rotate
against a seal between it and the secondary chamber.
Typically, these units are operated at a sufficient draft
to ensure that normal fluctuations in the burning rate
will not  result in a  pressure  above atmospheric.  In
addition, the  waste and supplemental  fuel  guns
typically are  mounted in  openings  at  the upstream
end of the kiln, and an overpressure would result  in
hot gases "backfiring"  past the  guns.  This  is  a
dangerous  situation  and  indicative  of  a poorly
designed or operated unit.
A  relatively  uncommon  rotary  kiln  design  is
particularly  sensitive to  overpressures  and  the
resulting fugitive  emissions. In the typical rotary kiln
design,  the  kiln  enters  the SCC  without  any
constrictions  in the gas stream following the rotating
seal. If the kiln, however, is attached to a seal leading
to  a  hot gas  duct  that  is followed by  an elbow,
diameter reduction, or other restriction to the hot gas
flow between  the two chambers, the  likelihood of
frequent overpressures increases dramatically.

For the majority of the hazardous waste incinerators
that a permit writer is likely  to encounter,  frequent
                                   fluctuations in pressure at the exit of the PCC usually
                                   indicate highly heterogeneous  wastes  that  burn
                                   unevenly  or periodic  overfeeding  of  waste to the
                                   incinerator.  If  the  overpressures  are sufficiently  high
                                   to result in fugitive emissions from  the seals or other
                                   openings between the PCC and SCC, they should be
                                   considered an  upset  condition  that  requires the
                                   shutoff of hazardous waste feed to the PCC.

                                   Limits on the PCC draft or pressure should be set in
                                   one of two ways,  one for  incinerators that are
                                   designed to operate  under positive  pressure and that
                                   are much more likely to tolerate a short overpressure
                                   without  releasing fugitive  emissions and  the second
                                   for those operating under negative pressure that must
                                   rely on  draft to keep the combustion gases in. Table
                                   2-3 summarizes  the  recommended  limits for the
                                   pressure in the PCC.
                                   For forced-draft systems, the automatic  waste feed
                                   cutoff for both  chambers should be set at the time-
                                   averaged pressure during the trial burn, provided that
                                   there  were  no  fugitive  emissions.  Brief  excursions
                                   above this pressure can  be tolerated  if they do not
                                                   16

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                                                                                                                 Ff
 Table 2-3.   Limits on Chamber Draft or Pressure
                     Forced Draft       Induced Draft
     	(Positive Pressure)   (Negative Pressure)
 Primary Chamber
Time-averaged     Slightly below
pressure determined  atmospheric
during trial burn     pressure
 Secondary Chamber  Time-averaged      Always below that
                  pressure determined  of the primary
 	during trial burn	chamber	
 exceed  the frequency and maximum excursion
 encountered during the trial burn.

 For  induced draft systems, the PCC  pressure  level
 activating  waste  feed shutoff can be the lower
 pressure of either of the following:

 1. Time-averaged pressure measured during the trial
   burn, or

 2. 2 mm water gauge  below atmospheric for the PCC.

 The 2-mm water gauge draft is only a guideline, and
 a  lower pressure should be  specified if highly  toxic
 materials are involved, or if the incinerator appears to
 have poorly designed  seals.

 If  pressure  variations  occurred during the trial burn,
 they can be permitted in the permit condition as  well;
 however,  the maximum pressure in the PCC  may
 never  exceed   atmospheric  pressure  under   any
 circumstances.  In fact, if the results of the trial  burn
 indicate the possibility of surges that result in a  PCC
 pressure in  excess of atmospheric, the operating
 conditions  of  the  unit should  be  evaluated  to
 determine  the  cause  of these surges,  and limits
 should be placed on other parameters such as waste
 feed and maximum  size of container waste to ensure
 that this type of surge  does not occur.

 It  is necessary  that  the maximum  pressure in the
 SCC must always be below that in the PCC to ensure
 that  any gases produced  in the  PCC are drawn
 directly into the SCC.

 One other  point should be  mentioned.  For those
 incinerators incorporating a rotary seal between the
 primary and  secondary combustion chambers,  it is
 important that the permit conditions include a  rigorous
 I&M  program for these seals  in addition to limitations
 on the size  and duration of the overpressure.  The
 seals between the  primary and  secondary  chamber
 are exposed to  high  temperatures, acid gases,   and
 mechanical  wear from  the  rotation. They must be
 properly maintained to prevent a release of unburned
 gases during a pressure surge.

2.7.5 Maximum Waste Feed Rate
 Regulation  40 CFR  264.345(b) requires that  a permit
 set limits on the  rate at which hazardous waste is fed
to the  incinerator. The limits on this parameter serve
 several purposes. First, they prevent overload of the
 combustion chamber and, thus, reduced  incinerator
 performance.  If low heating value waste is added to
 the  incinerator at too great  a rate, it may cool the
 flame  and  inhibit combustion.  Second, waste feed
 rate  limits keep the  residence  time above  the
 minimum level required to destroy the POHCs. The
 larger the fuel and  waste feed, the greater the flue
 gas  flowrate  and,  hence, the  lower  the  residence
 time. Also, limiting the waste feed rate also  limits (to a
 degree)  a group C parameter, the  heat released per
 unit  volume (see Section 2.3.2). Finally,  limits to the
 waste feed rates are often  necessary  to fix other
 parameters such as  chlorine or ash  feed rates.

 Two types of limits should  be placed on the total
 waste feed. The first is total waste  feed per unit time
 for each waste stream or waste stream type such  as
 solid wastes, aqueous wastes, or organic liquids. This
 limit is based on the  average over  time achieved
 during the trial burn.  The second factor that should  be
 regulated is the instantaneous waste feed  rate. This
 parameter  is referred  to  in Table 3-2  as the
 "maximum size of batches or containerized waste to
 the  PCC."  This is  a  group  B  parameter  but  is
 addressed in this section because of its close  relation
 to the maximum waste feed  rate.  The instantaneous
 waste  feed rate is not important if the waste is fed  by
 nozzles,  a continuous conveyor, or a screw feed. If,
 however, the  waste  is fed in  batches  as with  a ram
 feeder or in drums,  there is a  danger that the batch
 that  hits  the PCC can instantaneously either quench
 the flame if, for example, the waste  is aqueous or wet
 soil,  or result in an instantaneous release of heat and
 flue  gases  that exceeds  the  capacity  of the
 downstream air handling  system.  The latter  event
 would  result in puffing at  the joint between the PCC
 and  SCC and in fugitive  emissions, as discussed in
 Section 2.1.4.

 The  volatile content  of the waste influences the rate
 at which  such a sudden release  would  occur.  An
 excessive amount of volatile  material in a  waste will
 result  in  a rapid  release  of hydrocarbons,  which,  in
 turn, will  lead to a rapid increase in the PCC pressure
 and  an increase in the  CO level. A shutdown would
 be triggered on that basis. This event is  discussed
 further in Section 2.4.

 Drum feeding  of waste is particularly  susceptible  to
this  occurrence.  To illustrate, consider  the case
 where an incinerator  is  fed  one 208-L (55-gal)
 drum of  waste every 15 min  in   addition to other
wastes on a continuous basis. When that  drum hits
the kiln or grate, for example,  it will be cold, and it will
first  quench the flame and the burning waste in the
 PCC. As  it heats up, the drum will melt or burn, if it is
a fiber drum,  and  release the flammable material
within it.  A very rapid heat and gas release that may
 now  overpower the  gas handling system will result.
As discussed in Section 2.1.4, this release  can result
                                                  17

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 in puffing and fugitive emissions, or even if they do
 not occur, such an  event  can result in a significant
 change in the temperature  and the  residence time of
 the gases in the  SCO. This  change can affect  the
 destruction  efficiency and, hence,  the  ORE for  the
 POHCs.

 Such a scenario can be regulated  by designing  the
 trial burn to match both the mean and instantaneous
 waste feed rates for the incinerator.  For example,  the
 permit  condition  could specify  that a  given  waste
 stream  may not be  fed at a rate exceeding 300 kg
 (660  lb)/hr with  individual batches not exceeding 30
 kg (66  Ib) fed at no less than 6-min intervals. Other
 ways of specifying  this type of limit  such as  by
 maximum drum  size can be  used depending on  the
 unique  requirements of a given  system. Although an
 important factor, maximum volatile  content of  the
 containerized waste is not recommended as a permit
 condition  because it is impractical  to measure this
 parameter during continued operation. However, it is
 recommended that the containerized waste fed during
 the trial burn be chosen so as to equal the greatest
 amount  of  volatiles expected  during subsequent
 operation.
 The  above approach  needs to  be  modified  to
 consider  different waste  streams. An incinerator
 which burns all the wastes at a fixed feed ratio will be
 the exception rather than the rule. When a variety of
 wastes  are fed, the trial burn should be designed to
 incorporate a combination  of waste feeds to ensure
 sufficient operating flexibility. The limits on the waste
 feeds should be such that the combination of wastes
 fed at  any  one time  would result  in  a  total  heat
 release  rate in  each chamber that  matches the
 conditions in the test run.  Data from a test burning
 one set of wastes  should not be  used to set limits on
 the feedrate for a different  category of wastes, but a
 certain amount  of  flexibility  in the waste flows based
 on the above guidance is acceptable.

 In operation, the heating value of the waste does not
 have to be known  to great  accuracy to adhere to the
 variations in the waste feeds.  Typically, the operator
 will feed the waste with the lowest  heating value to
 the incinerator and then control the temperature at
 the exit of the combustion  chambers by varying the
feed rate of the wastes with higher heating values. If
the temperature cannot be maintained in this manner,
the operator can either lower the feed rate of the
 lower heating value wastes, use supplemental fuel, or
 vary the air feed  rate.
 This  procedure will  translate  into a reasonably
 constant  heat  release  rate  and,  under  most
circumstances,  a reasonably  constant flue  gas
flowrate. See the  Guidance  Manual for Hazardous
 Waste Incinerator  Permits  (3)  for further information
on how  the heat  release  rate  relates  to  flue gas
 flowrates. Appendix B also briefly describes  how the
 flue gas flowrate can be calculated.

 2.7.6 Air Pollution Control Equipment
 The final sets of  group A parameters that must  be
 limited with  permit conditions  are those relating to the
 APCE.  Typically,  the  APCE  on  a hazardous  waste
 incinerator removes acid gases (commonly HGI) and
 particulate.  There  are  cases  where either or both of
 these categories of pollutant do  not  require control.
 For example, if  the incinerator does  not burn
 halogenated wastes, no acid scrubber is required and
 no limits need to  be  set  on the respective APCE.
 Hydrogen chloride emissions will then  be regulated by
 limiting  the chloride content of the wastes so that the
 burning of halogenated materials  is limited. Monitors
 of HCI  emissions  may prove  to be an alternative for
 control  purposes.  Such monitors are now becoming
 available, and information on their reliability  is being
 gathered.

 Similarly, if  the system does not require particulate
 control  equipment (because the waste burned during
 the  compliance  test  did  not  contain  sufficient
 inorganic material  to form excessive particulate),  the
 limits should be placed on the amount of ash and the
 cleanliness of the quench water, if appropriate. These
 limits are discussed below.
Acid Gas Formation and Control
Incineration of  hazardous  waste  can  generate a
variety of acid gases such as SO2,  SOa, NOX,  HCI,
and  HF.  The NOx can be formed by oxidation of the
nitrogen  in the air and in the wastes. The other gases
are  typically formed  by the  chemical  reaction  of
sulfur,  chlorine, or other elements in the waste. The
most common  occurrence is  the formation  of  HCI,
and  in most hazardous waste incinerators, acid gas
control is synonymous with HCI removal. As a result,
the remainder of this  discussion will deal with HCI
removal.  The reader is  referred  to  the Guidance
Manual for Hazardous Waste  Incinerator Permits (3)
for  information  on the mechanisms  of  formation  of
this and the other acid gases.

Briefly, during combustion, the organic chloride in the
waste reacts with hydrogen from the waste,  fuel,  or
water in  the combustion  chamber to form  HCI.  A
small percentage (typically  3  to 5  percent) of the
chlorine  will normally be  released in the elemental
form  as  chlorine gas.  It  is  possible for  larger
quantities of free  chlorine  to  form  when  the
combustion chamber contains  an insufficient quantity
of hydrogen to convert all the organic chlorine to  HCI,
but because this is highly uncommon, it will not be
discussed further here. The permit writer is advised to
seek assistance from the Office of Solid  Waste if this
situation  is encountered.
                                                 18

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 Hydrogen chloride gas is readily soluble in water and
 is  most  commonly  removed  by  a packed-bed
 scrubber. It  can also be removed  by the scrubber
 used  to  control  particulate such  as the Venturi
 scrubber. Recent developments  in  "dry  scrubbing"
 technology has resulted  in incinerators utilizing some
 form of lime-slurry  injection  to  remove  the  acid
 gases.  The  variety  of acid  gas  removal devices is
 large.  Fortunately, for the purpose of setting permit
 conditions, the performance of these devices can be
 determined from the trial bum and, if it is shown to be
 adequate, the operation can be monitored with only a
 few readily measurable parameters.

 The RCRA  regulations  require that any  hazardous
 waste  incinerator which  emits  HCI at a rate greater
 than 1.8 kg  (4 lb)/hr must be equipped with an APCE
 whose  collection efficiency for  HCI exceeds  99
 percent. The actual performance of the scrubber is a
 complex interaction between the types of packing, the
 ability  of the system to distribute the flue gases  and
 scrubbants in the absorber intimately, the  alkalinity or
 acidity of the absorbant, and the liquid-to-gas (L/G)
 flow ratio. Of these, all but the last two are fixed for
 the facility and, if the compliance test is satisfactory,
 the design is assumed adequate.  Any changes in the
 design, however, constitute a change in the operating
 conditions   of  the  incinerator  and  should   be
 considered as a possible deviation from the permit.

 Four parameters need to be limited to ensure that the
 absorber  performs  as during the  compliance test.
 These  are (1) the L/G ratio, (2) the pressure of liquid
 feed to  the  nozzles,  and the pH  of the  aqueous
 solution (3) entering and (4) leaving the absorber. The
 UG ratio and the pH should  be specified  as no less
 than that measured during the successful compliance
 test. Because these parameters can be  controlled
 independently, there  is little  difficulty  in maintaining
 them within  constant bounds in a property operating
 incinerator, and variability does not usually have to be
 considered.  If variability does  occur during the  test, a
 time-averaged  value of these parameters should  be
 used. The pH of the aqueous solution entering  the
 scrubber should  be  limited  to  assure that  the
 scrubbing solution has adequate capacity to remove
 the acid gases. The pH of  the solution  exiting  the
 scrubber should  be  limited  to  assure  that  the
 scrubber is not being overloaded with acid.

 The pressure of the liquid feed  to  the air pollution
 control device should be a control parameter for the
 types of systems discussed below to reduce the  risk
 of deterioration of APCE performance. For many but
 not all types of scrubbers, this parameter, which is an
 indicator of how well the  scrubbing liquid (water)  gets
 distributed in the APCE, will  have a major  influence
 on  the equipment's performance.  Some simple
 scrubbers inject the  water into the gas stream
through one or more nozzles; others, such as packed
towers, can  have complex manifolds to distribute  the
 scrubbing liquid across the packing. In those cases,
 clogging or  deterioration  of  the liquid  distribution
 system (such  as  the  nozzles) could  result  in  a
 decrease  in  APCE  performance.  Clogging  or
 deterioration  of these systems would be manifest as a
 change in the  operating pressure outside the design
 range or the range determined  during the trial burn.
 Clogging  increases the pressure drop;  erosion  or
 corrosion  decreases the  pressure drop.  Because
 such failure is  usually gradual, nozzle  pressure does
 not  have  to  be interlocked with  an  automatic waste
 cutoff.  It should,  however,  be included in  the
 operating  log,  and significant  changes  in  it should
 initiate a corrective  action.

 An important type  of  control equipment where  the
 pressure of the water feed will not indicate a change
 in scrubbing  liquid  distribution  is an absorber which
 uses a distribution plate  to spread the water across its
 diameter. The water is released onto the plate, and it
 then  flows by gravity over the top of the packing or
 onto the  top  plate. In  this  case,  there  is little
 advantage to setting limits on the liquid  feed pressure.
 The pressure drop  across the column  along with the
 L/G  ratio, which  is a control  parameter,  will usually
 indicate a deterioration  in the liquid distribution  and,
 hence, scrubber performance. If possible, some form
 of regular inspection of the column interior, especially
 of the  water  distribution system,  is  desirable;
 however, a sight glass or inspection port  is usually of
 limited value  for  such  an   inspection.  A  good
 inspection, which usually  involves shut down of  the
 scrubber and  careful   examination  of its  innards,
 should  not   be normally  required  except during
 maintenance.

 Pressure drop  of the gas across the  scrubber is of
 operational concern in a packed tower,  but, except for
 a massive failure in the packing, deviation  from  the
 design  specification  is  unlikely to   cause  an
 environmental problem.  If liquid flow to the tower and
 flue  gas flowrates are monitored, pressure does  not
 need to be  in  the  permit  specified  for this type  of
 absorber.  It  should be  noted  that pressure  drop
 across a  packed  absorption  column  is frequently
 monitored and regulated for operational  reasons.

When a Venturi scrubber is  used  as  the  acid
 absorber,  pressure  drop  across the  scrubber will
 influence its performance. In that case, the  pressure
drop should be maintained  at a level at least as high
as that used during  the test. Again, because pressure
drop will be  a function of  L/G  ratio and of the throat
area  (for  a  variable throat Venturi),  there  is little
reason to expect major  variability  in this control
parameter.

A type of acid absorber which is coming into  more
common use  is a dry scrubber, which also is called a
spray dryer.  In  this  application, a slurry of caustic or
lime  is injected into the  flue gas,  and the  HCI reacts
                                                  19

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with  it  in  suspension. The reaction products  are
captured as  participate in  either a fabric filter or an
ESP.

When the acid absorber is a dry scrubber, neither L/G
ratio nor pH  has technical  meaning. In that case, the
limits in the  permit would  have to be based  on the
ratio of the flowrate of the  absorbent slurry to that of
the acid gas, i.e., "the system should not be operated
at a caustic or lime feed rate of less than X kg lime to
Y kg HCI," where X  and Y are determined from the
compliance tests. This type  of limit is  difficult to
enforce  since the  personnel  evaluating  the
performance  log would have  to  correlate the  waste
composition  and feed rate with  the  caustic or lime
feed rates to determine the acid production rate.

Continuous  HCI monitors   are  becoming  available
which,  based on EPA evaluations, appear  to be
sufficiently accurate and reliable to use  as a stack
sensor. The  output  of this type of monitor can be
used to control the caustic  or lime feed rates to a dry
scrubber. If  the applicant  chooses to  use  a  dry
scrubber for a  given  application, the permit  writers
should  consider requiring a continuous HCI monitor
whose output regulates the scrubbant feed to the dry
scrubber.

An HCI monitor is a  highly desirable feature for  any
incinerator that burns chlorinated species.  Its use  can
reduce  the  scrubber parameters  e.g.,  pH  and  L/G
ratios, that need to  be monitored. For example, an
HCI monitor in place at a facility that  uses a packed-
bed absorber for acid gas  control could be used to
control the absorber's operating parameters to ensure
the proper HCI release as  an alternative to  limits on
parameters such as L/G ratio, pH, and  pressure of
the nozzles. A continuous HCI monitor simplifies  the
permit,  operation, and enforcement  procedures. Its
use should be encouraged for all but the smallest and
simplest incinerators.

Paniculate Formation and Control
To understand the method of setting limits on  the
control  parameters for particulate  emission  control
devices in a hazardous waste incinerator,  it  is useful
to understand the major mechanisms of particulate
formation.  The  following  are  the  most common
sources of particulate formation in an incinerator:

1. Ash in the waste and supplemental fuel
2. Volatilization of metals and salts
3. Abrasion and  corrosion of the waste particles and
   the incinerator hardware,  refractory, etc.
4. Suspended and dissolved solids in the quench and
   scrubber water

Particulate releases  may  be  caused  by  other,
transient mechanisms as well. For  example, rapping
of an  ESP or the cleaning of the  bags in a fabric filter
 can result  in the  release  of a  large  amount  of
 particulate.  It  is important to ensure that the trial burn
 runs include such cycles of potential high particulate
 release. The  remainder of this discussion will deal
 with the mechanisms  relating to the  four sources  of
 particulate emissions listed above.

 The ash in the waste and in the supplementary fuel  of
 an incinerator will be released  during the  combustion
 process.  This ash  will  either be  entrained  by the
 solids  in  the  incinerator  and  leave with  the  bottom
 ash, or it will be carried  by the combustion gas into
 the APCE.  In the case of an  incinerator designed  to
 burn solids, the ash content of the fuel is  insignificant
 compared to  the ash of the solid  materials being
 burned; and this mechanism can be ignored in favor
 of  some  others discussed below.  Liquid  injection
 incinerators often do  not produce  a  bottom  ash.  In
 that case, the ash in  the waste and  the  fuel will  be
 released  as a  particulate and carried through  the
 incinerator into the APCE.

 The composition  of the inorganic fractions  of  the
 waste  and fuel can be extremely important when the
 potential air pollution  impacts from it are evaluated.
 Many compounds including metals  such as tin,  zinc,
 and lead and  salts such as sodium chloride will turn
 into vapors  at the  flame  temperatures  in an
 incinerator.  When the  gases containing  these vapors
 cool, as in  a  quench,  these materials form  very fine
 particulate often in the  1-um-diameter  or  smaller
 range. This  fine particulate is difficult for the APCE to
 remove. In addition, because of their  small diameter,
 these particulates present a  respiratory hazard. The
 potential health risk from many of these particulates  is
 due to both their very fine size and their  toxic metal
 content.

 Abrasion of  the wastes between the waste feed and
 the  refractory  is one  mechanism  for  particulate
 formation, especially when waste, such as paper, has
 a large amount of friable ash;  however, the particulate
 formed  by this  mechanism is  usually very large  in
 diameter and is readily removed by most types of air
 pollution control devices. The burning  of solid  wastes
 with these characteristics should trigger an evaluation
 of whether an  APCE is needed.

 The final  source of  particulate  emissions  is not
commonly  considered   when an  incinerator  is
evaluated. When water is injected  into the hot flue
gas to cool it, a significant fraction of  the water is
 evaporated.  Any suspended or dissolved solids in the
water are then released  as a  fine particulate. Often,
the quench and scrubber water  is  recirculated  or
 comes  from a  source of wastewater.  Even  if the
water used  for this purpose   is  once-through  well
water,  it may  contain  a  sufficient  level  of dissolved
salts (hard water, even when softened, is an example)
to release significant amounts of particulate. Limits on
solids  in  the  ash  and  water are  discussed  as
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 "minimum scrubber  blowdown,"  under  "group  C"
 parameters.

 The  particuiate  that  is  produced  by  these
 mechanisms is controlled by the APCE. The  most
 common  type  of  APCE used  on incinerators is  an
 impaction  scrubber,  usually of the Venturi design.
 Other  particuiate  control  devices used are  fabric
 filters,  ESPs, and  ionizing wet scrubbers (IWSs). The
 concept for each  is discussed briefly  in Appendix B
 and in greater depth  in  the  references  given  in
 Appendix A.

 The most commonly  used APCE on an incinerator is
 a  Venturi scrubber. This  device  is discussed above
 concerning  acid gas removal.  Figure 2-3  illustrates
 the  effect of particle diameter and  pressure  drop
 across  the  scrubber on Venturi scrubber  collection
 efficiency. As can  be seen, very large pressure drops
 are required to achieve high collection  efficiencies  for
 submicron particles.

 Figure 2-3   Effect  of pressure drop on  venturi scrubber
           efficiency.
            1.0    2.0    3.0     4.0    5.0
          Aerodynamic particle diameter (microns)
6.0
The important control parameters that must be set to
ensure that  Venturi  scrubber performance  is
maintained are pressure  drop across the scrubber
and L/G ratio. Both should be specified as minimums
as determined by  the  trial  burn. Variations in the
values should not be large enough in most cases to
warrant concern  with  variability  of  the  results.  As
 discussed  earlier, pH  of  the scrubbant  is  Only
 important if the  Venturi is also used  for  acid  gas
 removal.

 Fabric  filters  (FFs)  are not  commonly  used for
 particuiate control  in hazardous waste  incinerators.
 This  situation is  changing as FF  technology is
 modified to fit the  new application. Fabric filters are
 sometimes used in conjunction with dry acid removal
 devices  as  discussed  above.  The  particuiate
 collection efficiency of an FF depends primarily on the
 following factors:

 • Fabric type and weave

 • Face velocity (gas  flowrate  divided  by the surface
   area of the filters)

 • Cake buildup on the filters

 • Frequency and level of cleaning of the bags

 It is normally only necessary to  specify the  minimum
 differential  pressure  across  the FF as  a  permit
 condition. This parameter is needed in order to shut
 off  the waste feed in case of a ruptured  bag. This
 value should be set as the minimum pressure drop
 observed  during any  successful trial  burn. When it
 becomes  necessary to replace one or more bags in
 the fabric filter, the bags can often be pre-coated by
 artificial  means  or by  burning  auxiliary  fuel. If
 precoating will not be  feasible, a lower  minimum
 pressure drop can usually be specified for the cutoff
 for  a  relatively short period of  time (under  an hour)
 until the new bags are coated  with filter cake. The
 particuiate  removal  efficiency of  new  bags  is
 somewhat  lower  until they  have been  coated with
 filter cake. Thus, it may be desirable to reduce the
 ash feed  or restrict the amount of metal or fume-
 forming wastes during  this period in  cases where
 there  is concern about excessive particuiate or metals
 emissions.

 Limits may  be considered  on other  parameters,
 including those listed above, but they normally are
 not needed. To illustrate, consider the consequences
 of setting limits on the frequency of cleaning and the
 upper pressure drop  across the bags. The point at
 which the bags are cleaned (by shaking, for example)
 is typically determined by the pressure drop  across
the FF. As the filters  accumulate dust, the  pressure
 drop  increases. When  it reaches a  predetermined
 upper value, the cleaning cycle is initiated. A limit on
the maximum pressure drop could identify problems
 in the cleaning cycle such as defective equipment or
 blinding  of  the filter media  but normally is not
 necessary.

An  excessive pressure drop will not normally  affect
APCE particuiate  removal performance  adversely.
 However, it may result in bag rupturing or "caving in,"
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which would then release excessive participate. When
such failure  occurs,  the  low pressure drop  cutoff
would shut down the waste feed and the incinerator in
an orderly manner. In theory, this scenario could be
handled by the  low pressure cutoff limit;  however, a
waste feed cutoff when the  pressure rises above a
maximum specified by the equipment design provides
additional time prior  to failure  and  is  highly
recommended when particulate removal efficiency is
a critical parameter.

The ESP is a well-established device for particulate
control.  It is usually used only in very large incinerator
installations.  For  a  given  installation  and  fixed
particulate loading, its performance is determined by
the  voltage  and  power  consumption in kilovolt-
amperes (KVA) approximately equal to kilowatts (KW).
Alternatively,  a minimum value  can similarly  be
required  for the  current  in mA and the  power
consumption  in  KVA. The permit should specify a
minimum value for the KVA as established in the trial
burn. It  should be noted that, at least in  theory, the
current  can go to zero when the  particulate loading
on the  input gas  stream is  very low. This is  not
common  because an ESP would normally not  be
used for installations where it  is  only  required
occasionally because of its high capital cost. If such a
situation is encountered,  additional guidance  should
be sought. One  possible approach in this case is to
maintain  the  minimum voltage  but suspend  the
minimum  current  requirement  under  selected
operating conditions.

The IWS  combines  the collection principles  of  the
ESP  with acid  gas removal of  a conventional
packed-bed scrubber. In  the IWS, the incoming
particles are charged  in a small ionized section with
high voltage  DC power.  Charged  particles  are
scrubbed  in  the packed-bed section.  During  the
operation, the  KVA  usage will vary  with  gas
composition. The only two factors that need to  be
regulated  are minimum liquid  flowrate (L/G  as  in  an
absorber)  and minimum DC  voltage. Both  of  these
should be the  minimum  measured  during the trial
burn.

2.2 Group B Parameters
The  group B  parameters  are those which  do  not
require  continuous  monitoring and,  thus,  are  not
interlocked with  the  waste  feed  cutoff. They  are
typically monitored  by sampling  and analyzing  the
wastes and controlling the  quantities of  wastes  being
fed  and  other  operating  parameters  for  the
incinerator. The  results of  these monitoring activities
are maintained in an operating log which is used to
ensure that the worst-case conditions established on
the basis of the trial burn are not exceeded.

Three classes of parameters are included in group B.
The first relates to the organic hazardous constituents
 that the incinerator is  allowed  to  burn and  to  the
 selection  of those (POHCs) that will be  measured
 during the trial burn to verify incinerator performance.
 The second limits the amount of halides and ash that
 the waste is permitted to contain so that the APCE is
 not overloaded. The third regulates  the quality of the
 water used for the scrubber and quench.

 As can be  seen, the group B parameters  are  very
 closely connected to  the group  A parameters
 discussed earlier. They are actually not different when
 the  impact on  incinerator operation  is  considered.
 They are  differentiated  here largely because  the
 group  B parameters  do not require  interlocks  with
 waste feed cutoffs as do the group A parameters.

 A category of parameters  that are  not  addressed
 under the incinerator regulations but may at times be
 important are those which influence the level of solids
 burn-down  that the  incinerator  achieves. This  is
 normally a function of the solids residence time in the
 PCC and it will affect the quality of the ash produced.
 This can be important in situations such as:

 • The applicant requests that it be "delisted"; that is,
   tested and shown not to be hazardous.
 • The waste  is subject to land disposal restrictions
   under 40 CFR 268.
 • The  incinerator is  used  to  destroy   toxics
   contaminating  a material,  such  as soil, for the
   purpose  of returning  it to  a  site which  is not
   necessarily  a hazardous waste disposal facility.

 In all of these cases, the incinerator is  intended to
 achieve a specific,  maximum level of  contaminant in
 the residues or ash.  This may  be  achieved  during
 operation  by  setting  limits  on  the  maximum  kiln
 rotational  speed  at a  value  where  the  ash was
 determined  to meet the applicable  criteria.  As
 discussed above, these conditions are not specifically
 required under the incinerator regulations, but can be
 included in the permit to address other regulations, or
 when determined  necessary to  minimize risk from
 contaminants  remaining in the residues,  under the
 authority of the  "omnibus" provisions  of  Section
 3005(c)(3) of RCRA, as amended.

2.2.1 POHC Selection and Incinerability Ranking
 The type and amount of POHCs in the waste are very
 important  to  the overall  performance  of  the
incinerator. This information  is typically  specified  by
the applicant when the waste streams that are to be
burned are identified.  The only permit condition that
needs to be placed on POHCs is one which specifies
that  no  hazardous  organic constituents which were
not represented in the waste burned during the  trial
burn may  be burned  in the  incinerator  during
subsequent  operation. The condition should also
specify that  only those waste streams that contained
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the specified type of POHC during the trial burn may
contain it during operation.

For  example, if  a  POHC  representing  chlorinated
aliphatic compounds only exists in one type of waste
stream  during  the  test,  it  cannot be introduced in
another one.  Types  of waste  streams  refer  to
categories  of waste such  as high  BTU, low- BTU,
aqueous, sludge,  or solid. A corollary to this limitation
is that no POHC different from that used during the
trial  burn  can be  introduced into a  combustion
chamber. The reader is referred to Sections 2.4 and
Chapter 4 for further  discussions  on  how  permit
conditions on POHCs are to be treated.

According to 40  CFR  264.342(b)(1), "One or more
POHCs will be specified in the facility's permit from
among those constituents listed in  Part 261, Appendix
VIII of this chapter, for each waste to be burned. This
specification will be based on the  degree of difficulty
of incineration of the organic constituents in the waste
and on  their concentration or mass in the waste feed
.  . . ,"  and  "Organic constituents which represent the
greatest degree  of  difficulty  of incineration will be
those most likely to be designated as POHCs

To satisfy this requirement, the permit writer must do
the following:

1. Designate  (or approve the applicant's  designation)
   the POHCs that will be measured during the trial
   burn
2. Based on the results of the trial burn, identify those
   organic compounds  that may  be burned  in the
   system during  operation,  i.e., those that are "less
   difficult" to incinerate

To satisfy this requirement,  it  is necessary to have a
method of  ranking Appendix VIII compounds into an
order of "degree  of difficulty of incineration." Such a
ranking  is commonly referred  to as an "incinerability
ranking" or "incinerability index."

At present,  many  EPA Regional Offices use a ranking
system  based on the  heat of combustion of the
Appendix VIII organics as a guide for selecting those
POHCs that are the  most difficult  to  incinerate.  This
system  is  described in the  Guidance  Manual for
Hazardous  Waste Incinerator Permits (3).  The higher
the heat of combustion of a compound, the easier it
is assumed to be to incinerate.  This procedure  is
presently under review, and data now being gathered
by the University of Dayton Research Institute (UDRI)
indicate that more appropriate ranking systems  may
exist. A draft of the UDRI Ranking  system (called the
TSLoO2 ranking)  and  the  rationale  for  its  use  is
presented in Appendix  D. This work is  still under
review.

Incinerability indices  other than heat of  combustion
can be used without a regulatory change because the
 regulations  do not mention  a specific incinerability
 hierarchy. This was done to allow flexibility in POHC
 selection. At  the time OSW  developed the current
 regulations, it was recognized that changes may
 occur  as new data became available.  Thus, thermal
 stability at low oxygen may be used as a criterion for
 POHC selection. Additional considerations that can be
 applied to POHC  selection  include concentration of
 the constituent in  the waste stream (the  higher the
 concentration, the more likely the compound is to be
 chosen as a POHC), toxicity (choosing a  particularly
 toxic compound in the  waste  to be sure it is
 destroyed),  and compound  structure  (choosing  a
 compound  to represent each  of the  structural
 classifications of compounds such as aromatics and
 chlorinated  compounds in  the waste).  Finally,
 availability  of  sampling and analysis  methods for
 potential POHCs and whether it is a common PIC are
 other considerations.

 When  the thermal  stability  ranking is used, it is
 recommended that POHCs  be  chosen from those
 compounds for which actual experimental  data exist.
 Because the  ranking will  be changing as additional
 laboratory testing  is done,  compounds fairly close
 together in  the  ranking  should not be  considered
 significantly different with respect  to  incinerability.
 Therefore,  when there  are testing  or availability
 problems with the preferred POHC,  it  would  be
 reasonable to  choose another POHC from the same
 class.

 Some  of the  compounds  in class I  of  the  TSLo02
 ranking present sampling and analysis problems. For
 example,  reactive compounds such as hydrocyanic
 acid and cyanogen  and water  soluble compounds
 such as acetonitrile would  require either   special
 sampling techniques or alternative POHCs. Sampling
 and  analysis  problems  should not be  encountered
 with compounds such as  chlorinated  benzenes.
 Guidance on  POHC selection will be  issued  in the
 near future.

 2.2.2 Maximum Halides and Ash
 As  discussed  in Section  2.1, the  amount  of acid-
 forming compounds (usually halides) will affect HCI
 emissions, and ash in the wastes and the  amount of
 dissolved  and suspended solids in  the quench and
 scrubber water will  affect the particulate emissions.
 The  permit  conditions must  include upper limits on
these parameters.  The  maximum  amount of acid-
forming compounds  which may be burned  in  the
 incinerator during normal operation should be set at
the maximum  that  was burned during  the trial burn
 (assuming the trial burn  demonstrated compliance
with performance standards).  Care must be-taken to
ensure  that when  more than one  acid-forming
material is burned,  the condition reflects the amount
of total  alkalinity  required  to  remove  them. For
example,  in  a case where sulfur-  and chlorine-
bearing compounds are  burned,  sulfur  will consume
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 two equivalents of alkali while chlorine will consume
 only one. This situation is uncommon,  but  the limit
 should be written to include these factors.

 Limits are set on the maximum amount of ash in the
 waste  that  may be fed to an  incinerator to avoid
 emissions of  excessive particulate and  overloading
 the APCE. For the purpose of this analysis,  ash can
 be defined as any constituent of the waste that, when
 properly burned, forms  a  particulate in the stack.
 These can include a number of inert materials  such
 as sand, dissolved compounds  such  as  sodium
 chloride or  inorganic elements, metals,  and  metal
 salts.

 In general,  the total  amount of ash that may  be
 burned  in an  incinerator is limited by specifying the
 maximum total ash  feed rate  that  met  particulate
 emissions limits during the trial burn. There are times,
 however, when it is necessary to place restrictions  on
 specific components  of that  ash.  The following
 discussion outlines some of the circumstances when
 such restrictions should  be considered.

 For  example,  consider the  following  hypothetical
 waste feed:
Waste Stream
A
B
Ash Components, kg/hr
10 - Si02
5 - NaCI
Silicon dioxide (as opposed to silicanes or silicones
which are organosilicon compounds that can  form a
fine  particulate  fume) is  not volatile under  the
conditions of a  typical incinerator;  sodium chloride
can volatilize and form a fine particulate. Assume the
trial  burn  demonstrates  acceptable  particulate
releases at  these maximum feed  rates of the  two
compounds.

Based on these tests, the total ash feed rate normally
could be limited  in the permit to 15 kg (33 lb)/hr. If,
however, the amount of sodium chloride is increased
and  silicon  dioxide decreased during operation, an
increase in the fine particulate loading  to the APCE
and  in the total  released particulate could  occur. If
this  release appears  to be of  concern,  the  permit
condition might specify a total maximum NaCI feed of
5 kg (11  lb)/hr as well as a  limit on the total ash feed
rate. If B is the  only  waste stream likely to contain
NaCI, that  limit  could  be converted to  a  maximum
feed rate and NaCI concentration for waste stream B.
While this conversion  reduces operator flexibility to
blend wastes, it  also  reduces  the  need for waste
analysis  during  operation and  makes the ash  limit
easier to enforce.
 Typically,  fine  particulate can form  from  ash
 containing the following categories of materials:
 • Sodium salts, especially sodium chloride
 • Volatile  metals  such  as  mercury,  lead,  tin,
   antimony, arsenic, and chromium
 • Inorganics whose  oxides  are  volatile  under the
   conditions of the combustion  chamber
 • Silicon-organic  compounds  such  as silanes or
   silicones

 When these conditions are encountered, the effect of
 an increase of  the  fine  particulate loading  on the
 APCE  should  be  explored,  and,  if  necessary,
 restrictions  on the amounts of such components of
 the ash should be included in the permit conditions.
 These restrictions should  be considered  especially
 when the waste includes Appendix VIII metals. Feed
 limits for individual metals should be set where metals
 emissions are of concern as outlined in Guidance for
 Permit Writers for Limiting  Metal  and HCI Emissions
 From Hazardous Waste Incinerators (4).

 Another  important parameter  related to particulate
 emissions is the APCE inlet gas temperature. Certain
 types of  particulate,  especially  the  fine  particulate
 discussed above,  form in  the  incineration process.
 They form  as gases  in the combustion zone  and
 condense as the temperature decreases downstream.
 The amount of condensed particulate is a function of
 the temperature.  As the temperature to  the  inlet of
 the  APCE  increases,  less  of this "condensible
 fraction" enters the APCE as a particulate subject to
 collection.  It can  condense  as  a   particulate
 downstream,  typically  in  the  stack.  Under  this
 scenario,  as the  inlet temperature  to  the  APCE
 increases, particulate  emissions would also increase.
 As a result, the  maximum APCE inlet temperature
 should be the maximum  measured  during  the  trial
 burn. To  protect  the  APCE from damage  due to
 excessive temperature, this level should not be higher
 than the  manufacturer's specification for maximum
 temperature.

 2.2.3 Maximum Batch and Container Size
 The maximum size of batches or waste containers
 fed to the  PCC is  recommended  as  a  group B
 parameter because of the effect of the instantaneous
 waste feed  rate  on  the ability  of  the  incinerator
 system  to  maintain  steady-state  operation  and
 minimize phenomena  such  as instantaneous  oxygen
deficiencies, puffing,  and flame quenching.  This
 parameter is discussed along with  maximum waste
feed rate in Section 2.1.5.

2.2.4 Minimum Particulate Scrubber Slowdown
The final group B  parameter  to be discussed is the
scrubber blowdown. As discussed  in Section 2.1,  it is
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 possible for participate to be produced in the quench
 and even  in the scrubber. The greater the amount of
 solids present in the quench and scrubber water,  the
 greater  the potential for paniculate to  be produced.
 The operator of an incinerator controls the quality of
 the  scrubber  water by varying the fraction of  the
 water leaving the scrubber that is recycled back to it
 and the fraction being "blown down" or discharged.
 The larger the blowdown, the  cleaner the scrubber
 and quench water tend to be. The permit writer limits
 the  degree of contamination  of  the scrubber and
 quench  water by specifying  the minimum amount of
 blowdown during operation.

 Clearly,  blowdown is only an issue when the scrubber
 and quench utilize recycled water; for example, when
 the (liquid) water leaves the scrubber and quench is
 collected in some form of reservoir such as a tank,
 sump,  or   pond where it  is  partially  treated and
 neutralized. To control  the quality of the water in the
 reservoir, a fraction of it is sent to the sewer or other
 discharge   (the blowdown),  and  the  remainder is
 recycled to the incinerator.  In some incinerators, the
 blowdown  can come from a reservoir in the scrubber
 or quench  equipment.  In cases where once-through
 water enters the  scrubber, "blowdown  rate" has  no
 meaning,  and  no limit needs to  be  set  for this
 parameter.

 The minimum  blowdown rate for  the  incinerator
 cannot be  easily  determined directly from  the trial
 burn. If  the operator starts the trial burn  with clean
 water and  then uses the normal blowdown rate, the
 scrubber water will  start  clean and then  become
 contaminated with dissolved and  suspended solids.
 The trial burn can,  therefore,  show a satisfactory level
 of particuiate removal, but this could  be due  to a
 transient phenomenon associated with this technique.

 One method  of reducing the probability  of such  an
 occurrence is to  design the trial burn  so that the
 system  is  operated for a sufficient time before the
tests to ensure that the quality of the water in the
 sump has  reached steady state. For example,  the
 applicant could be required to  have not cleaned the
 sump or changed the water for  a  specific pretest
 period.

Another approach would be to  specify the blowdown
 rate such that the combined dissolved and suspended
 solids in the scrubber  and  quench  water pond  or
 sump do not exceed the mean determined during the
 successful  trial burn with  the  highest  solids in the
quench and scrubber water.


2.3 Group C Parameters
 Recommendations for group C parameters are based
on  the  need to  ensure that  incinerator operation
adheres to  recommended  combustion   and APCE
operating practices. These  practices, which include
waste liquid and  slurry  burner  settings,  APCE inlet
 gas temperature, and  maximum heat input for each
 incinerator  chamber  consistent with  design
 specification, are based  strictly on  design  limits and
 equipment manufacturer specifications.  Thus, permit
 conditions for these parameters are  not based on trial
 burn conditions, and compliance verification does not
 require continuous monitoring, although maintaining
 records in the facility operational logs is necessary.

 2.3.7 Burner Settings
 The  burners in liquid  injection  and  afterburner
 chambers should  be  set  to  operate  according  to
 manufacturer design  and  operating  specifications.
 These settings  should also  be consistent with the
 ability  of  the burners  to atomize  the  liquid waste
 properly  and  promote  efficient  mixing. These
 specifications vary  according  to  the waste  burned,
 burner and nozzle type,  and method of  atomization.
 To restrict the operation of these burners to trial burn
 settings possibly would constrain the operation of the
 facility and  limit  the  types of wastes  that  can  be
 incinerated, which is not the intent  of the  permitting
 procedure.  The  permit should  allow  sufficient
 operational  flexibility  in  waste  viscosity,  burner
 pressures, and  turndown limits as long  as these
 settings are  compatible  with burner  manufacturer
 recommendations. Additionally,  a  minimum  waste
 heating value should be  set in a permit for burners
 providing  100 percent of the heat input to a liquid  or
 afterburner chamber. A liquid waste with  a  LHV  of
 11,600 kJ/kg (5,000 Btu/lb) should be  sufficient  to
 maintain  a  stable  flame  consistent  with good
 operating practices.

 2.3.2 Total Heat Input
 The total  heat input  requirement  states  that  the
 incinerator should not be allowed to operate beyond
 its  design capacity.  Typically, maximum heat input
 and maximum  temperatures are not important
 considerations for the permit writer  because facilities
 are rarely  subjected to operation outside manufacturer
 design specifications.  Because such operation  can
 result in  refractory damage, it may be  self-limiting.
 To  exceed them will also result in exceedance  of
 other  imposed permit  conditions  such as  the
 maximum waste feed rate  and  combustion gas
 velocity. Thus, compliance with the incinerator design
 heat input capacity  is considered  good  operating
 practice and  should be  a permit condition for  the
 facility as  long as the limit imposed is consistent with
 the other control parameters. The maximum  total heat
 input  would  normally   be  the   manufacturer's
 specification for the equipment; however, if  a greater
 heat input is successfully  demonstrated during  the
 trial burn, it may be specified instead.

2.3.3 APCE Inlet Gas Temperature
 Typically,  some reduction in the temperature of the
 incoming gases  is required to comply with material
 specification of the downstream equipment. For FFs,
the maximum inlet temperature  is  specified by  the
                                                 25

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type of cloth material. This temperature limit can vary
between  120 and 290 °C (250 and 550 °F) for an FF;
for a dry ESP,  the inlet gas temperature affects the
particulate resistivity  and,  thus, the performance of
the ESP.  In this context,  it is difficult  to  specify a
maximum inlet  temperature because this parameter
depends  on the type of control equipment and its
manufacturer. Therefore, it is  recommended that the
permit  writer  obtain  the  equipment design
specifications from the  permit applicant and that the
operating temperature be defined according to those
specifications. It may, however, be necessary  to set
the maximum temperature limit at a lower level, as
discussed  in   Section  2.2.2  (concerning fine
particulate formation) to  assure  that all  particulate
forming fumes condense prior to entering the APCE.


2.4 Other  Parameters
Below are listed a number of  parameters  that were
considered but not selected as control parameters:

•  Minimum oxygen concentration

•  Maximum  gas  volumetric  flowrate,  maximum
   velocity, or  minimum  residence time  in  each
   combustion chamber

•  Maximum  volatile content of containerized waste

•  Minimum  total heat input to  each combustion
   chamber

•  Maximum  kiln slope

•  Maximum  kiln rotational speed

•  Minimum liquid flow to the Venturi scrubber

The rationale for not selecting these parameters is
discussed below. It is recommended that the permit
writer consider  this  discussion  and  note that  to
impose more permit conditions may not necessarily
improve   compliance   since many  parameters
interrelate and each condition  has an effect on  the
operational flexibility of the unit.  However, if the  unit is
unique in some manner,  some  restriction on  the
above or  other  parameters may be desirable. This
contingency, while unlikely  with  fairly  standard
incinerator designs, cannot be ruled  out in all cases.
The permit writer is urged to seek  assistance from
the Office of Solid Waste when  an unusual  design
appears to require that conditions  be  set for any
parameters  not specifically recommended  in  the
guidelines.

While the complete combustion of POHCs  and PICs
requires the  presence of sufficient oxygen,  there are
several major  arguments against setting  minimum
limits on oxygen. The most important reason is  that it
is difficult to pick one oxygen level that is satisfactory
for the combustion of a wide variety of wastes. An
oxygen limit based  on one type of waste would not
necessarily be adequate for destroying other wastes.
While it may be theoretically possible to determine a
suitable "worst-case" feed to test  oxygen  demand
during the trial burn, it is extremely difficult to do  so
for facilities that burn  a range of waste compositions
because of  the lack  of detailed  knowledge on the
mechanisms of  waste destruction. Fortunately,  it is
unnecessary to  set such a  limit for the  following
reasons:

•  Insufficient  oxygen  results  in  a  rise in  CO
   concentration. Because CO  is already  a permit
   parameter,  to limit oxygen as  well  would be
   redundant.

•  It is difficult to continuously and reliably measure
   oxygen concentration at combustion chamber exit
   conditions;   thus,  oxygen measurements  are
   normally made at the  stack. Often,  air inleakage
   occurs between the combustion chamber exit and
   the stack. The oxygen in this leakage air can mask
   oxygen deficiencies in the  combustion chamber,
   thus  limiting  or  negating the  value  of such
   measurements.

•  Several combustion chambers are  designed  to
   operate  under  oxygen-starved  (pyrolytic)
   conditions  with  additional  air  supplied  in
   downstream   combustion   equipment.  Minimum
   oxygen requirements for these pyrolytic chambers
   would be inappropriate and unenforceable.

To monitor  residence  time,  it  is  conceptually
preferable to monitor the maximum  gas  flows  or
velocities in  each chamber rather than the flue gas
flowrate  or  velocity  at  the  stack,  which  is
recommended  in Section 2.1.3. For the  majority  of
incinerators, however, the gas  flow in the stack or the
duct leading to  the APCE correlates reasonably  well
with that in each chamber, especially in the SCC, and
it is far easier to measure. As a result, the gas flows
in  each chamber do not need to be measured in most
circumstances.

It should be noted that in cases when there is reason
to  believe that a significant amount of air infiltration  or
other gas addition occurs between the SCC and the
point at which the stack velocity is being measured, it
may prove necessary to add some form of additional
monitoring  of  gas  velocity.  The  permit writer  is
advised to seek outside guidance in these cases.

The maximum volatile  content of containerized waste
was not selected as  a control parameter because it is
difficult  to measure during  operation  and  because
other control parameters  will  be impacted should a
highly volatile material be in a container. An excessive
amount of volatile material in a container of waste will
result in a rapid release  of  hydrocarbons. These
releases will manifest themselves in several ways.
                                                26

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 First, the pressure in the PCC will increase. Second,
 the  added hydrocarbons  will  starve the  flame  and
 increase the  CO level.  If  neither of these increases
 result  in  the  triggering of the alarms or  automatic
 shutoffs, the  increases  can  be deemed to be within
 the capability of the system.  If, however, the limits on
 these  two parameters  is exceeded,  an  automatic
 shutoff of the waste feed will  be triggered. In either
 case, there is no need  to regulate the volatile content
 of the  containerized waste.

 While  these  guidelines  do not recommend that the
 maximum volatile content of the  waste  be set as a
 permit condition, it is recognized  that  to  feed
 excessive amounts of  highly  volatile materials in
 containers is  not desirable. It is suggested, therefore,
 that the type  of containerized waste chosen for a trial
 burn contain the largest  amounts of volatiles expected
 in continuous operation.

 The minimum heat input to each combustion chamber
 was not  selected as a control parameter as it is very
 difficult to measure during normal operation and it is,
 in reality, specified  by the minimum temperatures of
 each combustion  chamber.  If  the heat  input  to  a
 combustion  chamber  is reduced, so,  also, is  the
 temperature.  If the heat input is reduced too much, a
 temperature cutoff will  occur. There is  normally little
 need to regulate both parameters.

 The kiln slope and rotation  speed were considered
 but not chosen as control parameters. The slope was
 not  chosen  because  it  is fixed at  the  time  of
 construction.  It  cannot  be changed  (except,
 conceivably,  in very  unusual  designs)  without
 rebuilding the incinerator, which would require a new
 permit or a modification to the existing one. The kiln
 rotational speed has a major influence on  the quality
 of the ash  and a minor  one  on the  particulate
 emissions. It  was not chosen  because there are, at
 present,  no  incinerator  regulations pertaining to the
quality of the ash  and because its  impact on  the
 particulate emissions is  small.  The ash quality, while
 not addressed under the incinerator regulations, can
 be  important  if the applicant  requests  that  it be
 "delisted" or  subjected to  other requirements as
discussed in Section  2.2.  Then,  limits of the
 maximum kiln rotational speed may be necessary.
A kiln's rotation rate also can have an impact on the
particulate released  from the waste.  An increase in
kiln rotation will result in the "grinding" of the ash and
its increased  release into  the flue gas. Fortunately,
this type  of particulate-forming mechanism results in
large  particulate which can easily be removed by a
well-designed  APCE. In almost  all  cases, the kiln
would have to rotate much faster than prudent
operation  dictates to generate sufficient particulate to
overload the APCE.  Therefore, there  is little need to
restrict  kiln rotation  rate  for  this purpose  unless
incinerator particulate emissions during  the trial burn
are close  to the maximum allowable.

The  final  parameter  that was considered  and  not
chosen as a control  parameter is the minimum liquid
flow  to the Venturi  scrubber. Minimum  L/G  ratio,
which is closely related, was selected  instead. Venturi
scrubber  efficiency can be related to the L/G ratio
and the velocity through  the Venturi.  Because  the
pressure  drop across a Venturi is a  function  of  the
liquid  and the gas flow and  because the gas flow and
velocity can be related to the  flue gas  flowrate, permit
limits  on the minimum pressure drop across a Venturi
and maximum flue gas flowrate are sufficient. There
is no need to set a limit on  the minimum liquid flow to
the Venturi scrubber as well.


2.5 References
1. Engineering  Handbook for Hazardous  Waste
   Incineration. EPA  Publication SW-889. September
   1981.2.

2. Hazardous  Waste Incineration  Measurement
   Guidance Manual. Midwest  Research  Institute.
   1988. (Draft under EPA review.)

3. Guidance Manual for Hazardous Waste Incinerator
   Permits.  Mitre  Corp.  NTIS PB84-100577. July
   1983.

4. Guidance for Permit Writers for Limiting Metal and
   HCI  Emissions  From   Hazardous  Waste
   Incinerators.  Versar,  1988.  (Draft  under  EPA
   review).

[A brief description of each  of these documents  is
presented in Appendix A.]
                                                 27

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                                             CHAPTER 3
                                     Setting Permit Conditions
Chapter 2 discussed the control parameters  for an
incinerator and  how they  interrelate  and affect  the
performance of  the incinerator system.  This chapter
discusses how the limits on the operating parameters
are determined and converted  to the conditions in the
permit.  The same strategies that are used for  setting
permit  conditions are  also used to  determine  the
conditions such  as temperature and  waste feed rate
at which the incinerator should be operated during the
trial burn. In both cases, it is  necessary to identify a
range of conditions broad  enough to  allow  the
operator sufficient "elbow room" in which to operate
but still  ensure that the incinerator operation  complies
with the environmental  regulations,  i.e.,  ORE,  HCI
emissions.

The conditions in a permit for an incinerator could
encompass many more factors than those discussed
in Chapter 2. These can be related to other features
of the installation; for example,  the  presence of an
emergency  vent stack, or the  burning of  waste
materials  which  are unusually toxic  or  of  extreme
concern to the local population. This handbook  only
discusses the setting  of permit  conditions on  the
system  and operating parameters.  It  is  limited to
those system and operating parameters  discussed in
Chapter 2. The  reader is referred to the appropriate
manuals listed in Appendix  A for guidance on how to
set other permit conditions.

This chapter begins with a discussion of permitting
approaches that  may be  used  by the applicant. It will
then discuss how the control  parameters covered in
Chapter 2 interrelate and how  variations in their trial-
burn  values  should be  handled.  It  will end  with
specific  guidance for setting permit conditions for the
permit approach  used. First, however, it is worthwhile
to define several terms relating to the trial burn.

A  trial burn  is the testing that is done to determine
whether  an  incinerator  can meet the performance
standards and to determine the operating conditions
that should be set  in the permit. A  "test"  must be
done  for each set of operating conditions for  which
the applicant desires to be permitted. Three replicates
or "runs" must be performed for each test.  One  set
of conditions constitutes  a  test; the overall trial burn
consists of one test for  each set of  operating
conditions. Each run of a test must be passed for the
incinerator to be permitted to operate at that set of
conditions. If the permitting authority determines that
there is good cause,  one run  may  be  thrown  out
provided that the permit conditions do not include any
operating conditions at  which the incinerator  was
shown to be out of compliance with the  performance
standards.
3.1  Permitting Approach
Three approaches  to  permitting  incinerators  are
suggested in  this guidance. Table 3-1  summarizes
them and  highlights some of the major advantages
and disadvantages of each. The approach that should
be used for a given incinerator is determined almost
completely by  the number of different combinations of
wastes and waste types that would be burned at  any
one time. The  three approaches are called:

1.  single  waste/single operating condition  ~ single
    point

2.  multiple waste/multiple operating  conditions --
    multiple point

3.  multiple waste/single operating condition  --
    universal

The  third approach is the most commonly  used and
can, in reality  be used for all incinerators. The single
point approach is a subset of the  universal approach.
It is presented as a separate method of setting permit
conditons  because it can be   used to  permit a
relatively  common  category  of  simple incinerators,
those that burn  only one  set of  well-defined wastes.
The multiple point approach is a relatively uncommon
method  of setting  permit  conditions;  it  can  be
considered as  a variation to the single point approach.

The first approach, the "single point approach," is the
least complex. It applies to incinerators that burn only
a well-defined set  of waste streams and operate
under unvarying  operating  conditions.  Hence  the
name  "single  waste/single  operating  condition."
These dedicated units are typically located at the site
where the  waste is generated and operate  in an  on-
off  mode,  where  "on"  is defined by a  relatively
                                                 29

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Table 3-1.
 Objective
Permitting Approaches
                         Approach
        Advantages
       Disadvantages
 1.  Single waste/single conditon
    "single point"
 2. Multiple waste/multiple
    condition
    "multiple point"
                Determine one set of operating
                parameters based on trial burn
                tests on a series of progressively
                worse conditions (single point)
                Determine multiple sets of
                operating  conditions, each
                applicable to a specific mode of
                operation  (multiple point)
 3. Multiple waste/single condition  Determine one set of universal
    "universal"                operating conditions
                            (universal conditions)
• Closely related to conditions
  tested
• Well-defined operating
  conditions
• Closely related to conditions
  tested
• Well-defined operating
  conditions

• Operational flexibility
• Easily enforced
• Constraining
• Constraining
• Potential redundancy
• Requires detailed support
  documentation
• More complicated to enforce
• Complex trial burn
• Requires greater engineering
  evaluation of trial burn data
constant composition, waste feed  rate and  operating
temperature. An example of  a facility that  could be
permitted with  this type of approach is one  which
burns a specific high BTU waste, a specific low BTU
waste  and  a specific sludge. Each of these  waste
streams  come from  one  or  two  well-defined
processes.  While  the  composition  and  amount of
each waste stream could vary, it only does  so within
narrow bounds.  No  new hazardous  constituents
(whether organic or metal) are introduced.

For  these facilities,  the permit objective  may  be
satisfied by setting  limits on the specific type of waste
to be  incinerated  and on the operating  parameters.
The permit conditions  are based  on one  trial burn
test. The wastes burned during this test are the  actual
wastes normally burned possibly fortified with some of
the POHCs for ease of sampling and analysis. During
operation,  no changes in the waste composition or
source are allowed.

The second approach,  called  here the  "multiple
point"  approach,  is  to  set multiple  limits  for  ech
operating  parameter:  each limit is based on  individual
test conditions or  modes of operation investigated in
the trial burn. This approach is  typically  best  suited
for incinerator facilities dedicated to treating a well-
defined  set  of  hazardous  wastes  of  uniform
composition; for example,  when drummed  waste is
burned with liquid  wastes A and B,  then one  set of
operating  conditions  apply. When bulk  solids  are
burned with wastes C and  D and waste  gas, then a
second set of operating conditions apply. As can be
seen, the  multiple point approach is equivalent to
setting a  series of single point conditions for  the
incinerator when it  burns a discrete, consistent mix of
wastes. Each mix  of  wastes must be defined  in the
permit.

The conditions  for multiple point permits are readily
defined, but the enforcement agency needs  to  be
aware  of  the operating mode to  verify   compliance
with operational  limits. For example, to verify that the
incinerator is operating at the proper conditions for a
given mix of wastes,  it is necessary to check the log
of the waste types  being fed at the time and  compare
                                            it to the logs of the control parameters. Nevertheless,
                                            because the  permit conditions are based strictly on
                                            the results of the trial burn, the multiple point strategy
                                            is recommended  whenever  the incinerator  will be
                                            operated at more  than  one condition.  There are,
                                            however, situations  when  neither  approach  is
                                            appropriate.  Thus,  a third  approach  is  suggested
                                            below.

                                            The third approach, referred to here as the "universal
                                            approach,"  is  to  develop  one  set  of operating
                                            conditions which allow a  given facility  to  burn a
                                            relatively broad  range of  wastes. Hence  the name,
                                            "multiple waste/single  condition."  This  approach,
                                            while being  the most complex, offers  the greatest
                                            operating flexibility. It is,  hence, the most commonly
                                            used one. The approach requires that the trial burn
                                            be carefully designed to represent the worst case mix
                                            of wastes and operaing conditions that the incinerator
                                            could conceivably encounter during  operation. One
                                            set of operating  conditions  is then set based on that
                                            test.  This approach allows  the incineration of a
                                            relatively wide  variety of wastes but  at conditions
                                            which are, generally, more severe than most of these
                                            waste streams require. One,  in effect, buys operating
                                            flexibility by requiring that the operating conditions be
                                            sufficiently  severe  to  burn  the   worst-case
                                            combination of wastes.

                                            The  greatest difficulty in using the universal permitting
                                            approach is designing the trial burn. If at all possible,
                                            it should be structured to achieve  with  one test the
                                            target limits  for  maximum  feed  rates  for all  feeds,
                                            minimum temperature, and maximum combustion gas
                                            velocity. This   may require  water   injection or
                                            exceptionally careful control of the  supplemental fuel
                                            compositions and feed rates during the tests. Energy
                                            and  mass  balance calculations  with  a computer
                                            program as described in Appendix E may be required
                                            to identify the condition that best satisfies the worst-
                                            case conditions.

                                            If it  is impossible to find a worst-case condition for
                                            the mix of wastes the applicant wants to burn, it may
                                            be necessary for him to accept less  than optimum
                                            target limits  for the  control parameters,  or  some
                                                   30

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         restrictions  on  waste feed  rates.  The  added
         complexity is well worth the  increased effort in the
         design of the test as it results in a single set of permit
         conditions that are  directly based  on the trial  burn
         without any need to  "massage" the data.

         It  is especially important when  the  trial  burn is this
         complex (although this  should  be done in all cases)
         that the  permit writer  and applicant  have  a clear
         understanding of the permit conditions that will result
         from  a  successful trial  burn at  the  conditions
         specified.  This gives  the  operator the  option of
         changing  the  test plan  to  achieve  workable
         conditions.

         In general, the simplest strategy that can  be used to
         set permit conditions  that still  allow  reasonable
         operating flexibility is the most desirable. As such,  a
         single  or multiple point  strategy is  preferable
         whenever the waste types burned justfy it. When the
         waste characterization does not allow it, the universal
         strategy can be used.

         At times,  the applicant may want to conduct tests at
         more  than one  operating condition  for "insurance."
         For example,  if he wants to operate the incinerator
         near the minimum temperature that will do the job,  a
         series  of  tests could be conducted at progressively
         lower temperatures. This situation   is  fundamentally
         the same as the case  when a  test is conducted at
         only one condition and  is clearly acceptable as  long
         as, in  the judgement of  the permit writer, no
         dangerous situations occur when the incinerator is
         pushed to its design limit. The permitting strategy in
         this case is the same as for the single point strategy.

         If a facility cannot achieve the critical target limits for
         all the contol parameters simultaneously, two or more
         tests  will be  required.  At that point,  the  question
         becomes  whether  a  multiple  point  or  universal
         permitting  strategy  is  preferable.  The discussions
         below address the advantages and disadvantages of
         each  strategy.  First, however,  it  is necessary  to
         discuss the  interrelationship  between the control
         parameters and how to treat normal data variability.


         3.2 Interrelating Control Parameters
         In  many  cases, the guidelines for setting  permit
         conditions from certain control parameters may be in
         conflict. For example, as the  temperature is raised,
         the gas  density decreases, and the gas  residence
         time  falls.  Limits  cannot,  therefore,  be   set
         independently on temperature and gas flowrate since
         they interact so  closely.  Most of  the  parameters
         discussed  in Chapter 2 are interrelated to a certain
         degree. To address this  interrelation in  an orderly
         fashion so as to avoid detailed system modeling
calculations, it is convenient  to  order the  control
parameters in the following groups:

1. Control parameters set from  trial  burn data that are
   related to waste destruction (Group A)

2. Control parameters set from  trial  burn data that are
   related to APCE performance (Group B)

3. Control  parameters that are independent  of  trial
   burn data (Group C)

These parameters are listed in order  of importance,
i.e.,  item 1  is more important  than item 2, which  is
more  important  than  item  3.  Individual control
parameters  within each group are listed in Tables 3-
2, 3-3, and 3-4, respectively.

It  is recommended that  limits  be set  on  the  control
parameters  according to this hierarchy. That is, the
permit writer should first establish the limit for the first
parameter  in group  1, i.e., minimum temperature in
each combustion chamber, then proceed down the
list,  making sure  that the limit  on  each parameter is
consistent with the limits on those above it.
Table 3-2.  Waste-Destruction-Related Control Parameters
          Set From Trial Burn Data
  Type
Parameter
   A    Minimum temperature at each combustion chamber exit

   A    Maximum CO emissions
   A    Maximum flue gas flowrate or velocity
   A    Maximum pressure in PCC and SCC
   A    Maximum feed rate of each waste type to each
        combustion chamber

   B    Maximum size of batches or containerized waste
3.3 Treatment of Variations in Data
Setting  final  permit conditions from  actual  data is
somewhat different  from setting tentative limits based
on a trial burn plan because the permit writer must
deal with data variability. Data can vary in three ways:

1. Variations with time within a single run

2. Variations  between repeats of the same  nominal
  operating conditions

3. Variations  due  to  changes  in the  operating
  conditions about the nominal operating point

Incinerators  do  not operate under  totally steady
conditions. Thus, most parameters vary  somewhat
with time over the  course of a single test run. The
k
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Table 3-3.  APCE-Performance-Related Control
          Parameters Set From Trial Bum Data

  Type	Parameter	

   A   Minimum differential pressure across participate venturi
        scrubber1

   A   Minimum L/G and pH to absorber1

   A   Minimum caustic feed to dry scrubber
   B   Minimum scrubber Wowdown rates or maximum total
        solids in scrubber liquid1
   A   Minimum kVA settings to ESP (Wet/Dry) and kV for
        IWS1
   A   Minimum pressure differential across a FF1
   A   Scrubber nozzle pressure
   B   Maximum total halides and inorganic ash feed rate to the
        incinerator system
   B   Minimum paniculate scrubber blowdown rate

  1 Select as applicable to APCE system.


Table 3-4.  Trial Burn Independent Control Parameters

  Type	.  	Parameter	        '

   C   Maximum total heat input for each chamber
   C   Liquid injection chamber burner settings
        • Maximum viscosity of pumped waste
        • Maximum burner turndown
        • Minimum atomization fluid pressure
        • Minimum waste heating value (if applicable)
   C   APCE inlet gas temperature
effects of this type of variation on the specification of
permit limits are dealt with in Chapter 2.

Random factors make it impossible to repeat exactly
the same nominal  operating  point.  Results  from
repeats  of the same nominal operating  point should
be averaged to yield a  single  mean value for  each
control  parameter  and other  performance.  For
example, three repeats of the same nominal operating
point  yield SCC  temperatures  of 1,100, 1,120,  and
1,090°C (2,010,  2,040,  and  2,000°F) and DREs  Of
99.996,  99.998,  and 99.990 percent,  respectively.
The composite temperature for that nominal operating
point  would be [(1,100 + 1,120 + 1,090)*3]  1,103°C
(2,017°F),  and  the  composite  ORE would  be
[(99.996 + 99.998 + 99.990) * 3]  99.994  percent.  It
should be noted that ORE values from  individual runs
at a nominal operating point may not be averaged  to
demonstrate compliance; for  example, 99.99 percent
ORE must be achieved for each  run. The calculation
of a composite ORE for a nominal operating point is
shown only for use in  the  equations  presented  in
Section  3.6.1  for interpolating between  two nominal
operating points.

How closely must the  data  match to  qualify as a
repeat of  a  nominal  data  point?  No  criteria  are
 recommended.  Variations are  unacceptable only  if
 they result  in  a  failure  to  meet  performance
 standards.  For  example,  if the last repeat  in  the
 example was performed at 1,000°C (1,830°F) and
 resulted in  a  ORE of 99.94 percent, that data point
 would be unacceptable because it resulted in a ORE
 lower than  the 99.99 percent performance standard.
 In such a  case, the  permit writer  must  exercise
 judgment on the proper course of action. A possible
 course  is to not use the "failing" condition as a permit
 limit. For example,  set  the  minimum  temperature
 above  1,000°C (1,830°F). An  alternative course  of
 action  may be to  require that a better repeat be
 performed.  Note that a "failing test" is defined as one
 in which any one of the three runs did not achieve the
 specified performance  goal. The  mean  ORE cannot
 be used to  show compliance if  all  runs did not show
 compliance.

 3.4  Single Point Approach
 The  single  point  approach  is the  least  complex
 permitting strategy suggested here.  It is appropriate
 for incinerators that burn  one  type  of  waste  with
 relatively constant  properties. Typically, this type  of
 incinerator is integrated into a process and  destroys
 the one waste stream to which it is  dedicated.

 Single  point permit  conditions  are  defined  as the
codification  of the  minimum demonstrated operating
 and  system  conditions resulting  in  satisfactory
 performance of the incinerator. They are set from one
 trial  burn test  (three runs minimum) with  each of the
 operating parameters established  as  described  in
 Chapter 2. The  order  of  setting  the  operating
 parameters  should  be that listed Jn  Section  3.2,
 although the order  is not usually, important, since the
trial  burn showed  the operating  conditions  to  be
 consistent with each other and realistic.


 3.5  Multiple Point Approach
A straightforward  variation  on an  incinerator  which
burns only one waste is one that burns a number of
well-defined sets of Wastes. Typically, these wastes
will be burned in combination; for example, a caloric
(high Btu)  waste  will  be burned  along with  an
aqueous waste stream. If the types of wastes to be
burned  can be  clearly identified,  i.e., waste  1=30
percent  stream A and  70 percent stream B,  waste
2 = stream C, etc.,  it is possible to specify that each
waste combination requires  a  unique set of  permit
conditions.

The  conditions for each point are arrived at by testing
the incinerator at each  clearly defined condition, and
if the test is successful, these conditions are  used for
the permit.  This approach  is actually equivalent to
setting single point conditions for each unique waste
                                                   32

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 stream combination and writing several sets of single
 point conditions.

 Such a  strategy is conceptually simple,  but unless
 care is taken to design the trial burn properly, it can
 prove to be difficult to both  implement operationally
 and to enforce. The conditions must be selected so
 that worst-case operating conditions are  met during
 each test with  that  set  of wastes.  The permit
 conditions are set for each unique waste combination
 in the same way as for a single point approach.

 3.6 Universal Approach
 For  most incinerator  applications,  it is desirable to
 select a  single  set of permit conditions to  apply to all
 modes of incinerator operation.  This approach  gives
 the incinerator  operator the flexibility  to deal with a
 variety of  wastes  and  waste  combinations  while
 limiting the number of trial burn data points that have
 to be gathered, i.e., every combination need not be
 tested. The universal  approach allows  such a set of
 permit conditions to be determined. It must be noted
 that this  strategy will typically require  a much higher
 degree of complexity in the trial burn and will result in
 operative conditons that  in  all cases are severe
 enough  to  destroy  the  worst-case  waste.  The
 interrelationships of the various operating parameters
 need to  be carefully  considered to  determine how
 worst-case conditions can be achieved for the major
 operating parameters simultaneously.

 The preferable method for  establishing the permit
 conditions under  a  universal  approach is to conduct
 the  test  under worst-case  conditions.  This
 procedure will likely involve blending  the wastes and
 adjusting the feed rates so that the applicant achieves
 maximum feed rates  for all  waste types, maximum
 feed rate of the POHCs, minimum temperature, and
 maximum  combustion gas  velocity  at  the same
 nominal operating point.

 It is usually possible to set the permit conditions from
 one set of trial  burn conditons with the proper choice
 of the test conditons.  For  example, worst-case
 values for temperature and combustion gas flow rate
 can  usually be achieved  at close  to worst-case
 values of the firing rates  of individual  waste streams
 by adjusting excess air and auxiliary  fuel.  If for  a
 given system  normal  variation of these parameters
 does not allow  this to  be done, it may be possible to
 adjust the  temperature and/or the  combustion  gas
flow rates by  injecting  water or  steam  to  the
 incinerator  during the  trial burn. In  this way,  the
 applicant demonstrates  the  system  under worst-
 case conditions, and the permit writer can base the
 permit conditions on hard data.

 If,  in spite of best efforts to do so, the  facility cannot
achieve the critical target limits for all the control
 parameters during the trial burn at one combination of
waste feed rates,  excess air, etc., and this failure is
confirmed with mass and energy balance calculations,
it will be necessary to conduct the tests at different
conditions.  Usually,  some form  of  incompatibility
between the waste  streams  and the conditions that
are required to destroy them is indicated. Tests then
need to be conducted at two or more conditions.

When two tests  are necessary,  it is advantageous
that they be conducted  at the  same thermal duty,
temperature, and  combustion gas  velocity if  at  all
possible. While difficult to achieve maximum thermal
duty,  combustion  gas  velocity,  and  minimum
temperature  simultaneously,  it  is  not impossible  in
most cases.  It is often possible to adjust the excess
air,  inject water,  and use  synthetic or  modified
wastes. The condition that facilities may not be able
to achieve under  one set of test conditions  is the
simultaneous  maximum  feed rate for  all streams
combined.  This  can  be  achieved  by varying each
individual waste feed rate to maximize  its flowrate for
each individual test.  The  individual  feeds can be
varied to maximize different ones in different tests as
long  as  all  feeds  are present  in each  test in a
sufficient quantity to demonstrate 99.99 percent ORE
for the POHCs in that waste stream.

Maximum feed rates for each stream could still be
allowed   in  the  permit.  The  restrictions  on
temperature,  combustion gas velocity, and thermal
duty would prevent the operator from  maximizing all
of them simultaneously. Another way of looking at this
approach is that the total feed rate (i.e., thermal duty)
does not really change; only the individual component
feeds change.

An important caveat to this approach is illustrated by
the  situation when  one  stream   contains  a
preponderance of particulate-forming or  acid-gas-
forming  constituents.  In that  case,  the above
restrictions can be used only to set the conditions on
those parameters that  impact the ORE.  The test at
which  the particulate and  HCI  parameters, for
example, are  worst-case would be used to set the
conditions on these parameters.

As stated earlier, the control parameters are grouped
into the three categories, A, B, and C, listed in Tables
3-2  through  3-4:


• Control parameters set (i.e., converted  to permit
  conditions) from trial burn data that  are  related to
  waste destruction

• Control parameters set from trial burn data that are
  related to APCE performance

• Control parameters that are independent of trial
  burn data
                                                 33

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The following subsections discuss  each  of these
three categories  and  how they  should  be  set as
permit conditions.

3.6.7 Control  Parameters  Related  to  Waste
Destruction
Control  parameters set from  trial burn data that are
related to waste destruction  are listed in Table  3-2.
As discussed above, these parameters should be set
directly  from tests at  a single value  for each
whenever possible. In those cases  when  it proves
impossible to minimize temperature,  maximize feed
rate of each stream, maximize flue gas flowrate,  and
maximize size  of  containerized waste at the same
time, these limits can be varied as  discussed in
Section 3.6, above. When the permit conditions must
be set on the basis of data  from different  trial burn
conditions, the following guidelines may prove  helpful.

The regulations generally consider temperature the
most important of the  control  parameters,  followed
closely  by  residence  time of  the gas  in  the
combustion chamber. The rationale for this  priority is
given in  Section 2.1.  Briefly,  it  is assumed that  in  a
properly operating incinerator, most of the  POHCs are
destroyed in  the  flame.  Of the fraction  that is not
destroyed in the flame, a portion will  be destroyed in
the  post-flame  zone. Post-flame POHC  destruction
occurs slowly and,  assuming all  other parameters
remain constant, will be a function of temperature and
residence time.  It is recognized that other  factors
such as turbulence and oxygen, or excess air, as  well
as  residence time  and temperature can affect  the
destruction of POHCs in the post-flame zone. Total
POHC destruction  is a  function  of incinerator
operating  conditions.  Thus, the destruction  of  the
small fraction  of  the  remaining  POHCs  can be
correlated with different and successful  operating
conditions. It is  critical  to  recognize  the basic
assumptions  and  limitations of  this relatively simple
approach. This type  of analysis  can be  used to
interpolate (but not extrapolate) the trial burn  results.

Basically,  the approach  consists  of  fixing  the
incinerator  operating  temperature  and relating  the
other parameters  to  it.  Limits on the maximum  flue
gas  flowrate  or maximum velocity measured at the
stack are then set to maintain the residence  time in
the SCC, which is inversely  proportional  to the  gas
volumetric flowrate in the SCC, to be greater than
that during  the  successful  trial  burn.  Whenever
possible, the  maximum flue gas flowrate should be
achieved during the test conducted at the  minimum
temperature by varying air flow,  injecting steam or
water into the system,  or by changing the fuel (or
waste) feed rate.

When this is  not possible, the minimum temperature
can  be  achieved  by reducing the feed rate of  the
waste or  auxiliary fuel. In this  case,  the  flue  gas
flowrate at the minimum temperature will be  less than
 the  maximum  flue gas  flowrate unless the excess
 oxygen can be increased proportionally. If the permit
 limit for the maximum flue gas flowrate  (or maximum
 velocity) is to be set from a test at a condition other
 than the minimum temperature, it must be  shown that
 the  flue gas  flowrate  at the minimum temperature
 could be increased to the maximum flue gas flowrate
 without  causing  ORE  to decrease below  99.99
 percent. This  involves  relating flue or  stack gas
 flowrate to ORE. The following theoretical  evaluation,
 which  is based on the above assumptions regarding
 the  dependence  of  ORE  on temperature  and
 residence  time, may be useful when  it  proves
 necessary  to  interpolate  data between trial  burns  at
 slightly different conditions.

 The first step in  the process is  to  relate the gas
 flowrate  in the stack to  that  in the SCC.  The gas
 flowrate in  the  stack is simply the flowrate of the gas
 leaving the SCC plus  air infiltrated and  the gas
 released by the  quenching procedure,  all corrected
 for temperature change. It can be written as:

 Qsec = (Qstack - Qleakage - Qquench) (Tse
-------
 associated with a trial bum. Equation 2 can be used
 with a reasonable degree of reliability in most cases.

 Next, the residence time must be  related to waste
 destruction. This is a far more difficult and dangerous
 step in the derivation. Nevertheless,  an approximation
 must be made if some means of interpolating the data
 is to be  used.  For this  type  of analysis, the DE
 (destruction efficiency)  is approximated  by a  first-
 order reaction according to the formula:
1 —
         \
          =
             100%/
                    = exp  -AT exp I -
                        F   ••     *
                      (3)
where A and E are  kinetic rate constants, R  is the
universal gas constant, I is temperature,  and x is
time.  For  a  particular  POHC  at a  constant
temperature, taking the natural logarithm of both sides
of equation 3 results in:
                Infl-
 DE \

100%/
                                    (4)
where K is a constant consisting of the terms within
the square brackets in equation 3 except for i.

Equations 3 and 4 assume that the destruction of the
small amount  of  POHC remaining in an  incinerator
which normally destroys more than 99.99  percent of
the  POHC will follow first-order reaction kinetics.
This is a reasonable approximation for the very low
concentrations of POHC in the gas phase  that occur
under these  conditions  and for   which  this
approximation  is intended. This  assumption  is
supported by the  results that have  been obtained by
the University of Dayton Research Institute  in its work
associated with development of  the stability rankings
given in Appendix D.

A  reasonable  way to  ensure the  ORE remains  at
99.99 percent  or  above is  to  base the  minimum
allowable  residence  time  (tmjn)  on  the  minimum
observed  ORE  (DREmjn) and the residence time at
the minimum-temperature trial burn point (Tmjn). For
this  analysis, it can  be assumed that  the minimum
ORE corresponds to the minimum temperature. This
assumption js a fallout of the assumption in equation
3,  although  this  will  not always  be  true  as the
mechanisms are more complex in actual operation.

In  practice, the DE  for a POHC is  not measured.
Rather,  ORE is calculated from measurements of
POHC emissions from the  exhaust  of the  APCE.
Although  small,  the  APCE's contribution  toward
POHC removal" will be the same from one test to the
next. The further approximation can be made that the
ORE is proportional to the DE. Without going through
the derivation, equation 4 can be rewritten as:
                                                                  In  1-
                                                          99.99% \

                                                           100%  /
                                                                                         (5)
                                                         TTmin
                                                                 In 1-
                                                          DRE  .
                                                          	nun

                                                           100%
                                            In other words, the logarithm of the  penetration (1-
                                            DE) for each  POHC is  proportional to the  residence
                                            time  and the  various  gas flows as described  in
                                            equation 2. Combining equations 5 and 2 reveals the
                                            following relationships:
                                                Q
                                                                            ORE
                                                                      In  1-
                                                                                 rrun
                                                                    100%
                                                 'stack max
                                                                 -9.21
                                                               "stack ^-  min
                                                                                         (6)
                                                     or
                                                                      Infl-
                                                                            DRE
                                                                       min
                                                                             100%
                                                  stack max
                                                                 -9.21
                                                                stack
min

  (7)
                                           where Qstack max  is  the  maximum  allowable  gas
                                           volumetric flowrate at the stack, and Vstack max is the
                                           maximum allowable gas velocity at the stack.

                                           Thus, if this equation is used to interpolate the results
                                           of trial burns at two slightly different conditions, the
                                           permit limit for  maximum flue gas flowrate measured
                                           at the stack (Qstack max) should be either Qstack max
                                           evaluated from  equation 6 or the maximum flue gas
                                           flowrate  measured  in  the  trial burn,  whichever is
                                           lower.  Similarly, the permit limit for  maximum  gas
                                           velocity measured at the stack  (Vstack max) should be
                                           either Vstack max evaluated from equation  7 or the
                                           maximum gas  velocity  measured  in the trial burn,
                                           whichever is lower.

                                           This approach should only be  used when the permit
                                           writer is faced with results such that one combination
                                           of waste feeds results  in  one value  of  the gas
                                           flowrate, the second combination results in a different
                                           value,  and the  applicant cannot accept the  lower
                                           value. Every effort should be made to avoid such a
                                           situation by planning the trial burn to  achieve these
                                           conditions simultaneously through use  of unregulated
                                           parameters such as excess air, as described earlier in
                                           this chapter. In  all cases, this  equation should never
                                           be used to extrapolate the data beyond that of a trial
                                           burn.  For example,  under no  circumstances  should
                                           this approach be used to allow a higher gas flowrate
                                           (and lower residence time) than measured in the trial
                                           burn.  The equations are not sufficiently rigorous for
                                                 35

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this purpose. They are given here as an interpolation
tool.
To illustrate the use of this approach, consider a trial
burn on a single chamber, liquid injection incinerator
with two POHCs at two conditions. The  first condition
is at a full waste flow to achieve the maximum flue
gas flowrate. The waste flow  is  reduced  for the
second  condition  to  achieve  the  minimum
temperature at  a flue  gas  flowrate  lower than the
maximum.  The  measurements may be summarized
as follows:
Run
No.
1
2
Combustor
Temperature, °C
1,200
1,000
Flue Gas
Flowrate, m3/s
20
17
ORE, percent
POHC1 POHC2
99.999 99.998
99.997 99.996
The maximum allowable gas  volumetric  flowrate
based  on  the ORE observed  at  the minimum
temperature  data  point  may be  calculated  from
equation 6:
   Q
                 /    99.
               In 1 - —
                 \      1(
 996% \

100%  /
    stack max
                    -9.21
         17 m3/s =19 m3/s
Thus, if 1,000°C (1,830°F) is set as the minimum
temperature limit, the minimum,ORE measured at that
temperature, 99.996 percent, is not enough to justify
setting 20 m3/s (700 cu ft/sec) (maximum measured)
as the maximum flue  gas flowrate. The flue  gas
flowrate limit should be set at 19 m3/s (670 cfs). Even
if Qstack max calculated by equation 6 were lower, 17
m3/s (600 cfs) would be set as the limit because the
incinerator  already demonstrated compliance  at the
minimum temperature at that flowrate.

To illustrate how temperature  and flue gas flowrates
can be made  to correspond so that the actual  trial
burn data can  be used for setting the limits on these
control parameters, consider the same example with
the change that the  tests be conducted to achieve
the minimum temperature by increasing the air flow.
The flue gas flowrate at  condition 2  would be higher
than 20  m.3/s (700  cu  ft/sec).  In  this  case,  the
maximum  flue  gas flowrate  and  the minimum
temperature permit limits could be set from the same
trial burn data point.

The maximum feed  rate  of each  low heating value
waste stream to each combustion chamber should be
that demonstrated at the minimum temperature  trial
burn point. This is reasonable for a low heating value
waste because an increase in waste feed leads to a
decrease  in temperature;  thus,  it  is possible to
minimize temperature and maximize  waste feed rate
at the  same trial  burn point.  For  a high-  or
medium-heating-value waste,  the  maximum feed
rate should  not be tied to the minimum temperature
trial burn because 1) it may not correspond to  the
maximize feed rate and minimum temperature and 2)
high heating value wastes are often used in  place of
auxiliary  fuel.  To  limit  the  feed  rate   to that
demonstrated at the  minimum temperature trial burn
point may severely  limit  the operator's  ability  to
control temperature.

A low heating value waste is defined as one incapable
of maintaining the incinerator temperature without  the
assistance of an auxiliary fuel or a high heating value
waste.  The exact  value that defines this cutoff
depends on the  character of the waste. A waste
whose LHV is less than approximately 11,600 kJ/kg
(5,000 Btu/lb) will generally have difficulty supporting
smooth combustion on its own. This very approximate
cutoff  is based  on  the requirement to maintain a
typical rotary kiln at 871 °C (1,600°F) at 100  percent
excess air.

The limit on  the maximum size of containerized waste
to the PCC is designed to prevent  depletion of  the
chamber oxygen from the sudden release of volatiles.
This  limit  should not  be  tied  to  the  minimum
temperature trial burn point because volatile release is
more rapid at higher  temperatures. It should  also  not
be  tied to the  highest temperature trial burn point
because there is no proposed maximum temperature
permit limit,  and  overcharging containerized waste to
the  PCC  should  cause CO  excursions which are
covered by other permit limits. Therefore, it  is
recommended that the limit on the maximum size of
containerized  waste  to  the PCC  be  set  as the
maximum demonstrated for any trial burn point.

In summary, the guidelines for setting permit limits for
parameters  related  to  waste  destruction  are  as
follows:

• Permit limits should only be set from trial burn data
  that show compliance with ORE, HCI, particulate,
  and CO performance standards.

• When applying the "universal" approach, every
  attempt should be made to achieve the  worst-
  case values of all key parameters during the same
  test.

• When the minimum temperature and maximum
  combustion gas velocity cannot be achieved during
  the same test, the  maximum  flue  gas .flowrate
  measured at the  stack  should be Qstack max
  evaluated  from equation 7 or the maximum flowrate
  measured in the trial burn, whichever is lower.

• The maximum feed rate  of each low heating value
  waste stream to each  combustion chamber should
                                                 36

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   be the feed rate of  that stream at the minimum
   temperature trial burn point; the maximum feed rate
   of each  medium- or  high-heating-value  waste
   stream should be the maximum feed rate  of that
   stream for any trial burn point.

•  The maximum size of containerized waste charged
   to the PCC should be the maximum demonstrated
   for any trial burn point.

3.6.2  Control  Parameters  Related  to  APCE
Performance
Control parameters set  from trial burn data that  are
related to APCE performance are listed in Table 3-3.
These parameters pertain to specific  particulate and
acid gas collection  devices. Control parameters that
pertain to particulate control devices include:

•  Maximum  total ash  feed  rate to  the  incinerator
   system    ,

•  Minimum differential  pressure across  particulate
   Venturi scrubber
•  Minimum kVA settings to ESP and kV to IWS

•  Minimum pressure differential across FF

•  Minimum particulate scrubber blowdown rate

The permit  limits for APCE parameters  relating  to
particulate collection devices should be set from  the
test performed at the worst-case  conditions for  the
APCE parameters while  the maximum amount of ash
feed is being fed  to the  incinerator. For an incinerator
burning solids, the  maximum flue  gas flowrate  will
entrain the maximum particulate.  In that case,  the test
should also be performed at the maximum flue gas
flowrate.  The  permit limits can  then  be set on  the
basis of this test.

In  those cases  where it  is either  impossible  or
impractical to achieve the maximum ash feed rate and
flue gas  flowrate  and maintain  the worst-case
conditions for APCE  performance.  It is  possible  to
use the results from several tests at similar (but  not
the same) values of the  control parameters and arrive
at  a technically justified limit. It  is important  to note
that this approach  is intended  only  to verify that
operating  limits for  different parameters, determined
from  two different  test  conditions,  are  mutually
consistent.  Under  no  circumstances  should this
approach be  used  to  extrapolate  values  of  any
operating  parameter beyond  a level  that has been
tested. Two  methods are  given,  one  for  a liquid
injections and the second for a rotary kiln incinerator.

For a  liquid  injection, the  particulate  loading (at 7
percent 62)  can be approximated over a  narrow
range of operating conditions as being proportional to
the ash feed rate and inversely proportional to the gas
flowrate.  The  gas flowrate enters into  this since a
higher  gas flowrate  will tend to  dilute  the particulate.
 Note that the 7 percent oxygen  correction does not
 influence the correction since the higher gas flowrate
 can be  caused by a  change  in fuels or waste
 composition rather than  by simple  dilution.  This
 generalization can  only be  made  when  comparing
 results of tests at similar, but not identical, conditions
 and it cannot be  used  to  extrapolate the  results
 beyond the conditions of any test.  If extrapolation is
 attempted,  assumptions on the  interaction between
 the gas  flowrate and oxygen correction, as well  as
 numerous  other factors invalidate  the  analysis. The
 above proportionality  can be represented by  the
 following equation:
                PC,
where:

   PC    = the particulate concentration (mg/dscm) at
           each of the two conditions, corrected to 7
           percent 02

   (mash) = the input rate of the ash to the incinerator
           at each of the two conditions

   Q     = flue  gas flowrate  at each of  the test
           conditions

This equation can be reconstructed to compare  the
emissions at a given set of hypothetical conditions
which are similar to a trial burn condition with the 180
mg/dscm limit  specified  by  the regulations  to yield
equation 8.
      PC,. ..
         limit
   180 mg/dscm
( m  ./Q .,  .  )
\  ash  ^stack/n
                      ash   stackymax ash, flue gas flow
                                              (8)
In equation  8, the subscript "limit "denotes the trial
burn at the  conditions of the limit of performance of
the APCE (minimum pressure drop, minimum KVA, or
minimum blowdown rate) and the subscript "max ash,
flue gas flow"  denotes the trial burn at the conditions
of maximum ash feed  rate and maximum flue gas flow
condition.

Equation 8 is  presented here mainly for the purpose
of illustration and to show  how a  similar equation is
determined for a rotary kiln  incinerator.  Interpolation is
rarely required to set conditions for a  liquid injection
incinerator.  Because  equation  8  is  rarely  used, no
separate example  of  its use is given. The following
                                                  37

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illustration for a rotary kiln incinerator can,  however,
readily be adapted to equation 8.

In summary, the  permit limit  for  the maximum
inorganic  ash  feed  rate  to  a  liquid  injection
incineration system should be set from the maximum
flue gas flow rate test conditions whenever possible.
If it is impossible to do  so,  limits for related control
parameters can be based on the results of more than
one test condition, although the test  conditions  used
must  be  as similar as  possible.  If this  is done,
equation  8  should  be  used to determine if the
"hybrid" conditions are internally consistent and will
still satisfy the regulations.

A  similar  analysis  can  be  done  for  rotary  kiln
incinerators.  In this  case, the participate  emissions
can (over a narrow operating range) also  be assumed
proportional to the ash feed  rate. However, for kilns,
the particulate emissions are generally recognized to
be proportional to the cube of the gas flowrate. This
is  based on  particulate entrainment for  kilns. Again,
this  is  a  rough  approximation to  assist  in  the
evaluation of similar tests. This fact cannot be  used
as a  predictive tool.  By using  these  facts in an
analogous way to the derivation of equation 8  one
can generate equation 9 for rotary kiln incinerators.
                          \mash^stack/limit
   PC.. ..
	limit

180 mg/dscm    /       3
                   ash "stack/maxash, flue gas flow

                                           (9)
                   y  ash "stack/n
If equation 9 is not satisfied, then the permit limit for
maximum inorganic ash feed rate or the permit limit
for maximum flue gas flowrate must be decreased by
decreasing the  value  of  the denominator  until  the
equation is satisfied. A combination rotary kiln-liquid
injection incinerator should be treated as a rotary kiln
incinerator since  most of the particle  loading  is
expected to come from entrainment in the kiln.

The  fpllowing  illustrates  the use  of equation  9.
Suppose  a  trial  burn is conducted  on a rotary
kiln/afterburner incinerator  at two test conditions. The
first test is run at full waste and air flows to achieve
the maximum flue gas flowrate and the maximum ash
feed rate. The second test is run at reduced waste
and the Venturi's  throat is adjusted to  achieve the
minimum pressure drop:

                                        Venturi DP,
 Test    mash,kg/s    Qstack-m3/s   PC.mg/dscm   cm H;O
1
2
1.0
0.5
20
17
150
50
50
40
     50 mg/dscm    (Q.5kg/s) (17m3/s)3

    180 mg/dscm
                                                                         0 kg/s) (20 m3/s)3
                                                                                         = 0.28:20.31
In this case, equation 9 becomes:
Since equation 9 is satisfied, the maximum inorganic
ash  feed  rate of 1.0 kg (2.2 lb)/s and  the  maximum
flue  gas flowrate of 20 m3/s (700 cfs)  can be taken
from test condition 1  while the minimum pressure
across  the Venturi scrubber can be  taken  from test
condition 2. If equation 9 were not used, then it would
be necessary to pick these conditions  at one or .the
other of the test conditions and set all  appropriate
parameters  on  that  basis,  thereby  making  the
condition more restrictive.

The  use of data from more than one test to set permit
conditions should be avoided if at all  possible.  The
following are a number  of general observations which
may prove  useful when designing  the trial burn so
that  one  test  condition  can be used to  set the
conditions.

Whenever possible, the  pressure  drop across the
Venturi  scrubbers should be adjusted  for a test by
changing  the throat  size  (if it  is  a variable  throat
Venturi) or, if that is not possible, by  adjusting the
liquid flow consistent with adequate  performance. It
should  not  be minimized  by lowering  the flue  gas
flowrate. This is especially important on rotary kiln
incinerators as  the  flue gas flowrate  has  a cubed
effect on the particulate emissions.

For  systems with  Venturi scrubbers,  the goal of the
trial  burn  should be to  achieve a minimum pressure
drop at the highest  gas  flow. For  fabric  filters,
pressure drop  can be  decreased by increasing the
cleaning frequency during  the tests.  In most cases,
the  particulate removal efficiency of a fabric  filter
increases  as the  cleaning frequency decreases,
although at a penalty of reduced bag  life.  A higher
than normal  cleaning frequency during  the  trial  burn
will result in a more severe test of the system.  To
increase the life of the  bags, a longer cleaning cycle
may  be desirable during normal operation. Allowing a
longer  cleaning  cycle  (within  good  operating
practices) will not  compromise  particulate  emission
levels.

Acid gas collection devices must meet a performance
standard of 99 percent HCI removal or a maximum of
1.8  kg  (4  lb)/hr emissions.  Permit parameters
pertaining to acid  gas collection devices include the
following:

• Maximum  total halide feed rate to the incinerator
  system

• Minimum water/liquor flowrate to the absorber

• Minimum p.H to the absorber
                                                  38

-------
Acid is  removed from the gas  by diffusing  to  and
dissolving in a liquid of high surface area. For  a given
physical  design  of the absorber, the critical  factors
determining  the  removal  efficiency are the L/G ratio
and  the  solubility  of  the acid  gas  in the solution,
which,  except at low  pH,  is usually high. As acid
gases  dissolve  and  are  removed  in  a  scrubber
solution, the pH of that solution decreases and results
ultimately in a  decrease in acid solubility  and  a
decrease in acid  removal  efficiency.

Typically, this efficiency loss is countered by removal
(blowdown)  and replacement of  a  portion  of  the
scrubber  solution and  by addition  of caustic to
maintain the  pH. The  most  severe  test  of  the
system's capacity to  remove  acid  from the  gas
occurs  when the total  halide feed rate is at  a
maximum, the pH of  the  scrubbing liquid  is at  a
minimum, the flow of the scrubbing liquid is  at  a
minimum, and the gas flow through the APCE is at a
maximum. These conditions^ will result in a minimum
L/G ratio, the highest acid gas loading, and the most
acidic scrubbant. Thus, the  permit limits for maximum
total halide  feed  rate to  the  incinerator system,
minimum L/G ratio, and minimum pH to the absorber
should all be set  from the same trial burn data point.

In summary, the  guidelines for setting permit limits for
parameters  related  to APCE  performance are  as
follows:  .
• Permit  limits  for minimum  differential  pressure
  across particulate Venturi scrubbers, minimum kVA
  settings  to  ESP  kV to IWS,  and  minimum
  blowdown rate for particulate scrubbers should be
  set at the trial burn  data point with the maximum
  total ash  feed rate  to  the incinerator system  and
  the maximum flue  gas  flowrate at the stack.  If
  these limits are set from a data point other than the
  maximum ash, maximum flue gas data point,  the
  maximum ash feed rate  and/or the maximum  flue
  gas feed rate limit should be reduced,  if necessary,
  to satisfy equation  9  for rotary kiln  incinerators.
  The permit limit for  minimum differential pressure
  across a FF is set from manufacturer specifications
  for new bags.
•  Permit limits for minimum L/G  ratio  and minimum
   pH to the absorber should be  set  from the trial
   burn data point at the maximum total halides feed
   rate to the incinerator system.

3.6.3 Control  Parameters Independent of  Trial
Burn Data
Control  parameters which  are independent  of  trial
burn  data are  listed in Table 3-3. Permit limits for
these parameters should be set independent of trial
burn  data  and  based   on   manufacturer
recommendations.
3.7 Determining Operating Envelope
Permit  limits  are  set  on  parameters  such  as
temperature and flue gas flowrate, which are reliable
indicators of incinerator performance. To meet these
limits, the incinerator  operator  must  maintain  the
system  within  an  implied  operating  envelope  of
control  variables  such  as  waste, fuel,  and  air
flowrates. With the exception of waste feed rates, it is
not necessary  or desirable to  directly  limit these
control  variables.  However, the  permit  writer, and
especially the permit applicant,  should  have  a clear
understanding of the operating  limits imposed by a
proposed  set of  permit conditions. This is particularly
important in the trial burn  planning stage when the
permit applicant has the  opportunity to examine the
consequences of the permit conditions  resulting from
the trial  burn plan and to modify the plan accordingly.
Before the trial  burn is approved, the  permit writer
and applicant should  agree  on  the set of permit
conditions that will result from the planned trial burn if
it is successful.

Energy and mass balance procedures such as those
described in Appendix E can be used to estimate the
envelope of operating conditions resulting from a set
of permit conditions. An  example of use of energy
and mass balance calculations  for this  purpose is
presented in Chapter 4. It is  recommended that,  for
flexibility in  the  permit conditions, these  kinds  of
calculations be performed by the permit  applicant.
                                                 39

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                                             CHAPTER 4
                                         Example Test Case
 The  purpose  of  this  chapter is  to illustrate  the
 previous guidelines for setting permit conditions for a
 typical incinerator facility. The example test case was
 developed using a hypothetical scenario intended to
 cover  typical  permit  objectives  and  trial  burn
 approach,  data reporting requirements, and trial burn
 data  evaluation. Although the facility design is based
 somewhat upon real systems and  trial burn results
 are  intended  to  represent actual  data,  any
 resemblance to an actual site is unintentional.


 4.1 Site  Description
 The  example incinerator is  an industrial  rotary  kiln
 system that  processes  a wide variety of hazardous
 waste streams. The incinerator, shown schematically
 in Figure 4-1, consists of two  combustion chambers
 followed by APCE. The PCC is a rotary kiln. The SCC
 is an afterburner.  The kiln can receive the following
 wastes:

 • Solids (either bulk or containerized) through a ram
   feed system at the front end of the kiln

 • Sludge through a lance at  the side of the kiln near
   the front end

 • Liquid organic and aqueous  wastes through  two
   liquid injection units in the front end of the kiln

 Kiln ash drops  down into  a  water bath  (sump), is
 conveyed up an inclined conveyor, and dropped into
 an ash hopper. Slowdown from the sump goes to the
 wastewater handling system.  This wastewater  system
 should be designed to meet all of the requirements of
 the National  Pollutant Discharge Elimination System
 which was  formulated in response to the Clean Water
 Act. (Wastewater treatment is not a subject covered
 in this handbook or example  test case.) The primary
 combustion gases exiting the  kiln are directed through
 the SCC. The SCC contains a waste burner with two
 liquid injection nozzles used to fire high heating value
.liquid organic waste. Natural  gas  is used  as  an
 auxiliary  fuel  to regulate  the desired combustion
 temperature in each chamber.

 Stack gases leaving the SCC pass through a quench
 section  and  a three-stage  IWS  before  being
 exhausted to  the  atmosphere via the induced draft
 (ID) fan and stack. The IWS consists of three stages
 in series, with twin parallel chambers in each  stage.
 The first  stage  is a  prescrubber (nonionizing).  The
 following two stages are IWSs. The scrubber system
 serves  for both particulate and  acid  gas  removal.
 Scrubber  liquor is  pumped through separate headers
 to each  of the  three  scrubber stages. The caustic
 flowrate  along  with  makeup  process  water  is
 regulated  to maintain a  pH of  approximately 6.5  to
 7.0. Effluents from the quench and all three  scrubber
 stages are combined  and flow to the wastewater
 system.  Key incinerator design  information  is
 summarized in Table 4-1.


 4.2 Structuring of the Trial Burn
 In this example case, the facility is  dedicated to the
 incineration of  onsite-generated  process  wastes.
 Individual  waste  streams to be treated  have typically
 consistent properties." That  is,  the physical  and
 chemical characteristics of each waste stream do not
 change appreciably  on  a  daily basis. Under  this
 scenario,  a multiple  point permit  approach  (see
 Section 3.5) may be appropriate. The assumption for
 this  example case,  however,  is  that  the  applicant
 seeks  a  single set of easily  enforceable  (universal)
 permit conditions that: 1) are consistent with  the daily
 operating  requirements of the facility, 2)  incorporate
 sufficient flexibility to satisfy anticipated  requirements,
 and  3) are compatible with the  safe  and economic
 operation  of each system component. Specifically,
 the applicant desires a permit that will:

 • Allow burning of any waste in any combination
  consistent with the equipment design and intended
  operation

• Allow  burning  of  any waste  at feed  rates
  established by storage and  process limitations  and
  consistent  with the  design  capacity  of  the
  incinerator

• Require  the minimum  auxiliary heat input, power
  consumption, and material (water, caustic) usage

• Require  the minimum number of trial  burn test
  conditions
                                                 41

-------
 Figure 4-1    Incinerator system for example test case.
       Natural Gas

     Liquid Waste —,
    Waste
      Water
  Drummed Waste
     Bulk Waste
                                                                                             *• NPDES
•  Not impose unnecessary  operational constraints
   and not impose extensive monitoring requirements

To structure a  trial burn  test  matrix  that  will
accomplish these objectives, four questions need to
be answered:

•  What  waste streams,  feed  rates,  and POHCs
   should be selected for testing?

•  What should be the operational settings of thermal
   treatment parameters?
•  What  should  be  the operational settings of  the
   APCE?

•  How many test  conditions  will accomplish  the
   objectives?

The  following sections summarize the rationale for
selection of trial burn test conditions, discuss the test
matrix, and  define  the resulting  permit  conditions
anticipated from this example test case.

4.2.1  Waste Selection and Feed Rates
The first  task in selecting trial  burn test conditions is
to  examine  the  individual  waste streams  and their
disposal  requirements to determine the waste  types
and quantities that should be burned during the trial
burn.  It is  necessary  to duplicate  the  most severe
conditions likely to occur during  actual operation and
to  identify those Appendix VIII (or other) compounds
that will be designated as the POHCs. As illustrated in
Figure 4-1, this facility incinerates three major waste
stream types:
•  Solids - containerized and bulk
•  Sludge
•  Liquid wastes

Table 4-2 lists the  eight waste streams that will be
burned at this facility and gives their major physical
characteristics and composition. Note the three waste
stream types  listed  above as well as  their  heating
value-high or low.  High  heating  value wastes are
generally those which will support stable combustion
on  their  own,  typically greater  than  11,500 kJ/kg
(5,000 Btu/lb)LHV.

The solid wastes that  will be  burned by this facility
consist of two streams identified  as S1  and S2. Of
these two, the "drummed waste,"  S1,  is the larger
stream. This waste  makes the  most severe demands
on  the incinerator's ability to  meet ORE,  HCI,  and
particulate  standards  because  it has  high
concentrations  of POHCs,  it  contains difficult-to-
burn Appendix VIII constitutents and has high chlorine
and ash contents. It contains 2.7  percent chlorinated
organics  consisting of  carbon  tetrachloride  and
trichlorobenzene,  which are potential  POHCs,  that
have a combined  maximum feed rate of 30.6 kg (67.5
lb)/hr. The solids waste stream, S2, is only about half
the size of the drummed waste stream, and the  only
potential  POHC in it is toluene at 0.5 kg (1.1 lb)/hr.
The applicant is requesting a permit to burn up to 27

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Table 4-1. Example Incinerator Test
Parameter
Incinerator type
Inside dimensions (diameter x length)
Cross-sectional area
Volume1
Heat capacity
Refractory thickness1
Refractory conductivity
Refractory surface area1
Cooled surface area
Waste feed system
Case: Summary Design
Units
-
m
(ft)
(sqft)
m3
(cuft)
kJ/hr
(Btu/hr)
cm
(in)
kJ/s-m-°C
(Btu-in/hr-sq ft-°F)
(sqft)
(sqft)

Information
Primary
Combustion
Chamber
Rotary Kiln
3.4 x 6.7
(1 1 x 22)
8.8
(95)
59
(2,090)
72 x 106
(68x106)
15
(6)
0.00144
(10)
88
(950)
0
(0)
Ram feed for drums and
bulk solids; sludge lance;
Secondary
Combustion Combined
Chamber System
Afterburner
3.6 x 7.5
(11.9x24.6)
10.3
(111)
78
(2,750)
36 x 106 108X106
(34x106) (102x106)
15
(6)
0.00144
(10)
106
(1,140)
0
(0)
Liquid injection
for organic
Installation date
ID fan capacity

Maximum quench inlet temperature1

Maximum scrubber inlet temperature1

HCI removal capacity1

Quench water supply capacity1

Quench water temperature1
                                          year

                                      Normal m3/min
                                        (dscf/min)
                                         kg/min
                                         (Ib/hr)
                                           Us
                                         (gpm)
                                                      liquid injection for organic
                                                      and aqueous
                                                               1981
                                                                                 1975
  1 Needed for energy and mass balance calculations.

kg/min (3,600 Ib/hr) of solids,  which can  be met  by
burning any combination  of S1 and S2.  Clearly, the
most  severe  case would  be to burn only S1 for the
test. If this is possible, a successful test will allow the
operator maximum operating flexibility. If the system
cannot burn only drummed solid waste, at least one
test should be performed at a combined feed of S1
and S2 of  27  kg/min (3,600 Ib/hr) with S1  accounting
for as much  as possible of  this value.  The permit
condition  would then  specify the  maximum  total
amount of  solid  waste  and maximum drummed waste
to be  burned.

As shown  in  Table 4-2, the largest liquid wastes fed
to the system  is  L1,  the contaminated wastewater
stream. The  high  concentration  of  water  in  this
stream is likely to tax the ability of the  kiln to maintain
temperature and prevent  quenching of the solid and
liquid  wastes.  The large quantity of water also results
in the largest gas  release per  unit  of  waste  and,
    570
 (20,000)

   1,090
  (2,000)

     96
    (205)

      3.18
    (300)

     19
    (300)

  4-38
(40-100)
                                                      hence, the  lowest gas  residence time  for  a given
                                                      combustion setting. Thus, L1 is a good stream to vary
                                                      to establish the liquid waste feed rate limit during the
                                                      trial burn.

                                                      The third  category of waste to  be considered is the
                                                      sludge  waste,  SL. This waste  will  not  sustain
                                                      combustion on its own.  It should be  included in the
                                                      test program because it  represents a separate waste
                                                      stream for which a feed rate limit must be determined
                                                      and because it will tend to quench the high  heating
                                                      value solid  wastes  in  the  kiln.  That  this  waste
                                                      contains  a potential  POHC, chlorobenzene, adds
                                                      weight to  including it in at least some of the tests
                                                      during the trial burn.

                                                      There are four high heating value liquid  organic
                                                      wastes.  These are fed  either to the kiln or to  the
                                                      SCC,  and neither  of these has a major advantage or
                                                      disadvantage as a candidate for the trial  burn. Below
                                                   43

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Table 4-2.   Example Incinerator Test Case: Major Physical and Chemical Characteristics of Onsite-Generated Wastes
Waste Type;
Category
Solids

Solids

Low Heating
Value Liquids

High Heating
Value Liquids
High Heating
Value Liquids
High Heating
Value Liquids


High Heating
Value Liquids
Sludge

Site
Waste
10
S1

82

L1


12

L3

L4



L5

SL

EPA
Waste
ID
Code
F005

F005




F002

F005

K016



1

K085

Waste
Description
Drummed
waste
Trash and
bulk solids
Organic
contaminated
wastewater
Liquid organic
waste
Liquid organic
waste
Liquid organic
waste


Liquid organic
waste
Sludge .

Location
Kiln

Kiln

Kiln


Kiln o rSCC

Kiln or SCO

Kiln or SCC



Kiln or SCC

Kiln

High
Heating
Value.
kJ/kg
(Btu/lb)
20.900
(9,000)
20,600
(8,900)
Nil


32,700
(14.100)
35.460
(15,300)
31,500
(13.600)


34.600
(14,900)
6,200
(2.700)
Moisture,
% wt.
4

20

98.67


15

2

2



10

70

Ash,
% wt.
45

39

0.07


1

2

0.8



3

1.4

TOCI,
% wt.
2.2

0

0.2


15

.0

26



5

0.01

Carbon,
% wt.
36

28

0.05


50

78

52.2



48

10

Hydrogen,
% wt.
9

11

0.01


16

10

15



20

3

Oxygen,
% wt.
3.8

2

1


3

8

4



14

2.99

RCRA App. VIII
Compounds
Carbon tetrachloride
Trichlorobenzene
Toluene

Chloroform
Toluene

Carbon tetrachloride
Tetrachloroethylene
Phenol
Toluene
Bis(2-chloro)ethylether
Carbon tetrachloride
Trichloroethylene
Trichlorobenzene
None

Chlorobenzene

Typ.
Cone.,
% wt.
1.1
1.6
0.1

0.14
0.02

6.8
10
26
16
1
18
6
5
NA

0.03

Disposal
Requirements,
kg/s (Ib/hr)
0.31
(2,500)
0.14
(1,100)
0.51
(4,000)

0.032
(250)
0.0063
(50)
0.096
(750)


0.0063
(50)
0.15
(1.200)
  1 Not a RCRA waste.

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 are the requirements for the liquid organic wastes that
 must be satisfied during the trial burn:

 1. Ensure that the maximum total organic chloride is
   fired so that the maximum HCI loading is put on
   the  scrubber.

 2. Ensure that sufficient levels of POHCs are fired so
   that 99.99 percent ORE is detected.

 It  is possible to  satisfy these conditions by firing the
 amounts of each of the L2 through L5 streams at the
 rates specified in Table 4-2. These are the average
 firing  rates  anticipated during  normal  operation;
 however,  in this  case,  the  applicant chose to  meet
 the  8.4 kg/min  (1,100 Ib/hr) combined disposal
 requirements for  these four streams by burning 2.28
 kg/min (300 Ib/hr) of the L2 waste in  the kiln and 6
 kg/min (800 Ib/hr) of the L4 waste in the SCC.

 The next  step  in the  process  is  selection  of the
 POHCs which will be burned during  the trial  burn.
 Since the guidance for this selection is still (as of this
 writing) not finalized, the following three POHCs will
 be arbitrarily chosen for the purpose of this example:

 1. Trichloroethylene (TCE)

 2. Perchloroethylene (PCE)
 3. Trichlorobenzene (TCB)

 Please see the final guidance on  POHC selection or
 contact the  OSW  for  further information on the
 selection process.

 4.2.2 Trial Burn  Operating Conditions
 When the individual waste streams and feed rates are
 selected, the temperatures and excess  oxygen levels
 are the primary operating conditions that need to  be
 established  for  these  combustion  chambers.
 Temperature settings have an impact on the amount
 of auxiliary fuels required because the permit imposes
 limits on  the maximum waste  feed  rate in   each
 chamber.  However,  for  this sample  case,  the
 applicant has the option of controlling temperature  in
 the SCC by waste feed only because the waste (L4)
 has  a  heating value significantly greater than 9,300
 kj/kg (4,000 Btu/lb) and can be used as the primary
fuel. Thus, by selecting the appropriate L4 feed  rate,
the use of auxiliary fuel can be minimized, and limits
 on waste feed rate can  be  increased. In spite of this
 option, the applicant's objective is to obtain a permit
for chamber outlet temperatures sufficiently  low to
 maximize  operational  flexibility.  These  target
temperatures are approximately 800°C  (1,470°F) for
the kiln and 950°C (1,750°F) for the SCC exit planes.

 The excess  oxygen  of about  11  percent  was
determined to be sufficiently high to permit operation
 close to the maximum gas flowrate for the system yet
 still within the ability of the ID fan to maintain draft in
 the kiln and design pressure drop in the APCE.

 Table  4-3  summarizes  the three  test  conditions
 selected for the trial burn. All tests will be performed
 with the same wastes and feed  rates. These feed
 rates were  selected to  reflect  maximum  anticipated
 loading to the incinerator and maximum chloride and
 ash handling by the APCE. Waste feed rates are also
 within  the  design waste  handling capacity of the
 incinerator  system.  The kiln and  SCC temperatures
 are reduced progressively  from the  first test to the
 third test. The natural gas fuel to  both chambers  is
 used  to control the temperature  so that maximum
 waste  feed  can be maintained  at  relatively  constant
 rates.  Energy  and  mass  balance calculations,  as
 described in Appendix C, can be used to estimate the
 natural gas feed rates necessary to achieve the target
 temperatures at 11  percent excess oxygen  for the
 selected waste feed rates. These calculations also
 determine the  flue  gas  flowrate for each operating
 condition.  The  "worst-case"   test  conditions  are
 investigated during the third test when temperatures
 to both chambers  are  lowered  to target levels
 selected by the applicant.

 If  the  incinerator satisfies  the  RCRA performance
 standards for ORE,  HGI,  particulate emissions, and
 CO emissions  at these  test conditions, it will  have
 shown  compliance under the   following   permit
 conditions for the combustion chambers:

 •  Minimum Temperatures
   -  Kiln: 800°C (1(470°F)
   -  SCC:950°C(1,750°F)

 •  Maximum Waste Feed Rates
   -  Solid waste  (drummed and/or bulk):  27 kg/min
     (3,600  Ib/hr) for 170-L (45-gal) drum size
   -  Sludge to kiln: 9 kg/min (1,200 Ib/hr)
   -  Wastewater to kiln: 30.6 kg/min (4,000 Ib/hr)
   -  Organic liquid  waste  to  kiln:  2.28 kg/min  (300
     Ib/hr)
   -  Organic liquid  waste  to SCC:  6 kg/min  (800
     Ib/hr)

•  Total Ash and Chlorine Feed Rate
   -  Ash: 1.38 kg/min (1,800 Ib/hr)
   -  Chlorine (CI'): 2.58  kg/min  (340 Ib/hr)
•  Maximum Gas Flowrate:  598 actual m3/min (21,000
   acfm) at stack conditions (71 °C,  160°F)
•  RCRA Listed Compounds:  Thermal  stability class
   equal to or lower than the tested POHC  (based on
   TSLoO2) in each waste stream

In  addition to these  limits, the facility would still  have
to  meet the CO emission limits,  maintain negative
pressure in  the kiln,  and  operate  the  liquid waste
burner  in the  SCC  according to  burner   design
                                                 45

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Table 4-3.   Example Incinerator Test Case: Trial Burn Test Matrix (Target Settings)
Kiln Waste Feed, kg/min (Ib/hr)

Test
No.
1

2

3

Drummed
Waste1
S1
27
(3,600)
27
(3,600)
27
(3,600)

SiudgB
SL
g
(1 ,200)
g
(1 ,200)
g
(1 ,200)

Wastewater
L1
30.6
(4,000)
30.6
(4,000)
30.6
(4,000)

High Btu
L2
2.28
(300)
2.28
(300)
2.28
(300)
sec
Waste Feed,
kg/min (Ib/hr)
High Btu
L4
6
(800) .
6
(800)
6
(800)

Total
Ash Feed,
kg/min (Ib/hr)
13.8
(1,800)
13.8
(1,800)
13.8
(1,800)

Total
Cl Feed,
kg/min (Ib/hr)
2.58
(340)
2.58
(340)
2.58
(340)


Temperature,
or\ toc\
O
PCC
goo
(1 ,650)
800
(1,470)
800
(1,470)
V ' 1
sec
1,040
(i.goo)
980
(1,800)
950
(1,750)

Average
Excess
02, %
11.0

11.0

11.0

  1 Drummed waste feedrate corresponds to 1 drum approximately every 6 minutes.
Table 4-3 (continued).    IWS Water Flowrate

Test
No.
1


Estimated uas
Use,
kJ/s (MBtu/hr)
Kiln
1,520
sec
3,780
(5.26) (12.g)
2

3

0

0

3,517
(12.0)
2,740
(9.5)

GasFlowtolWSi,
m3/min (cfm)
@STP2 ©Actual
510 614
(18,000) (21,700)
510 614
(18,000) (21,700)
490 589
(17,000) (20,400)
Quench
Gas
Outlet
Temp
°C (°F)
80
(176)
80
(176)
79
(174)



Water Flow, L/min (gpm)

Quench
910
(240)
887
(234)
gis
(242)

1
320
(85)
320
(85)
320
(85)
IWS Stage
2 3 Total
140 140 600
(38) (38) (161)
140 140 600
(38) (38) (161)
140 140 600
(38) (38) (161)

1 UG.
• Urn3
(gal/fiJ)
1.0
(0.0074)
1.0
(0.0074)
1.0
(0.0074)

IWS
Voltage
Settings
kV
30

30

30


IWS
Inlet
pH
7.0

7.0

7.0

Scrubber
Slowdown
Rate,
L/min
(gpm)
15:
(4.1)
15
(4.1)
15
(4.1)
  1 Assumed the same as stack flowrate @ STP.
  2STP = 20°C (68°F) and 1 atmosphere.
specifications  pertaining  to atomization pressures,
viscosity of the waste, and turndown.

4.2.3 Operating Conditions: APCE
The APCE trial burn test  conditions are selected by
the applicant,  taking into  consideration the ability of
the  APCE  to achieve  RCRA  compliance  with
paniculate  and HCI  emissions and its  feasibility to
maintain these operating  conditions during all  post-
permit incineration activities.

The operating conditions of the prescrubber and the
two  IWSs  will  be maintained  at  relatively constant
rates between test  conditions.  The critical scrubber
operating parameters that will be reflected  in the
permit are  listed  in Table 4-3. The total IWS water
flowrate is  targeted for 650 L/min  (160  gpm) for an
L/G  of 1 L/m3 (0.0074 gal/cu ft) with  an inlet pH of
7.0. The kV setting  for the two-stage  IWS is
targeted  for 30 kV, and the total scrubber blowdown
at 15 L/min (4.1 gpm).

4.3 Trial Burn Test Results
The trial  burn test consisted of three replicate  runs at
the same target test condition  but at each of three
(somewhat  different, acutal)  test  conditions.
Performance standards for ORE, HCI, and particulate
emissions were  passed at all test conditions. Time-
weighted  averages for  CO  stack gas  levels  were
below  the limit  values.  The  process conditions  for
each  run  are summarized in Tables 4-4 through 4-
6. The performance results are summarized in Tables
4-7  through  4-9. Further  supporting  data  are
included  in  Appendix  G.  An example strip-chart
recording for combustion  temperatures  is  also
included in Appendix  G along with example  logs of
CEM data for CO and oxygen and an example plot of
corrected  CO readings.


4.4  Determining   Limits  on  Control
Parameters
The results of the trial burn must now be converted to
a set of limits on all the  parameters listed in Table 2-
1. As  discussed  earlier, the  universal permitting
strategy will be followed as described in Section 3.6.
Under  this strategy,  one value of each  parameter
(e.g.,  temperature, gas flowrate,  and pressures),
including  allowances  for variability, applies to  all
modes  of incinerator operation.  The results are  a
readily enforceable set  of  conditions that  have  an
adequate level of operating flexibility.
                                                 46

-------
Table 4-4.    Example Incinerator Test Case: Summary of Process Operation Results1 • Test Condition 1

                                                                                  Run No.
Parameter
Test date
Combustion gas flowrate
PCC temperature
Mean
Maximum
Minimum
SCC temperature
Mean
Maximum
Minimum
PCC pressure
SCC pressure
Quench inlet temperature
Quench outlet temperature2
Heat input rate
Quench water flowrate
IWS inlet pH
IWS outlet pH
1st stage IWS water flowrate
2nd stage IWS3 water flowrate
3rd stage IWS4 water flowrate
IWS Unit 1 A - DC Current
IWS Unit 1A - DC Voltage
IWS Unit 18 - DC Current
IWS Unit 1B- DC Voltage
IWS Unit 2A - DC Current
IWS Unit 2A - DC Voltage
IWS Unit 28 - DC Current
IWS Unit 2B - DC Voltage
Stack height
Stack exit velocity3
Stack temperature3
Stack excess O24
Units
-
Actual m3/min
(acfm)
°C
(°F)
"C
(°F)
°C
(°F)
«c
(°F)
°C
(°F)
°C
(°F)
mm H2O
(in H2O)
mm H2O
(in H2O)
-
°C
<°F)
kJ/hr
(Btu/hr)
L/min
(9pm)
-
-
L/min
(gpm)
L/min
(gpm)
L/min
(gpm)
mA
kV
mA
kV
mA
kV
mA
kV
m
(ft)
m/s
(fps)
"C
(°F)
%
1-1
May 12, 1987
931
(31,800)
910
(1,670)
962
(1,763)
850
(1,562)
1,049
(1.920)
1,118
(2,045)
1,022
(1,872)
-1.6
(-0.10)
-8.6
(-0.34)
NA
79
(174)
74 x 106
(70 x 106)
852
(225)
6.3
2.9
321
(84.9)
142
(37.5)
142
(37.5)
33.8
30.0
21.1
31.1
94.2
28.2
105.4
28.8
18.3
(60)
12.5
(41.0)
71
(159)
10.85
1-2
May 12, 1987
956
(33,300)
916
(1,680)
968
(1,774)
860
(1,580)
1,038
(1,900)
1,115
(2,039)
1,020
(1,868)
-2.6
(-0.10)
-8.4
(-0.33)
NA
79
(172)
72 x 106
(68x106)
912
(241)
6.7
4.7
322
(85.1)
142
(37.5)
142
(37.5)
21.8
30.5
16.5
30.6
126.1
27.8
116.2
29.0
18.3
(60)
12.7
(41.8)
72
(161)
10.58
1-3
May 13, 1987
845
(31 ,300)
916
(1,680)
969
(1,776)
850
(1,562)
1,032
(1,890)
1,113
(2,035)
1,019
(1,866)
-2.5
(-0.10)
-7.6
(-0.30)
NA
77
(171)
69x106
(66x106)
965
(255)
6.8
3.9
322
(85.0)
142
(37.5)
142
(37.5)
14.2
31.0
10.7
31.8
94.4
27.7
81.7
28.5
18.3
(60)
11.8
(38.9)
71
(160)
10.68
 1 Average of readings taken during each run.
 2 Approximate IWS inlet temperature.
 3 Average of readings from two simultaneous MM5 trains.
 4 Orsat analysis.
                                                          47

-------
Table 4-5. Example Incinerator Test Case: Summary
Parameter
Test date
Combustion gas flowrate
PCC temperature
Mean
Maximum
Minimum
SCC temperature
Mean
Maximum
Minimum
PCC pressure
SCC pressure
Quench inlet temperature
Quench outlet temperature2
Heat input rate
Quench water flowrate
IWS inlet pH
IWS outlet pH
1 st stage IWS water flowrate
2nd stage IWS3 water flowrate
3rd stage IWS4 water flowrate
IWS Unit 1A - DC Current
IWS Unit 1A- DC Voltage
IWS Unit 1B - DC Current
IWS Unit 1B- DC Voltage
IWS Unit 2A - DC Current
IWS Unit 2A - DC Voltage
IWS Unit 2B - DC Current
IWS Unit 2B - DC Voltage
Stack height
Stack exit velocity5
Stack temperature33
Stack excess Og4
Units
-
Actual m3/min
(acfm)
°C
(°F)
°C
(°F)
"C
(°F)
°C
(°F)
°C
(°F)
°C
(°F)
mm H20
(in H2O)
mm H2O
(in H2O)
-
°C
(°F)
kJ/hr
(Btu/hr)
L/min
(gpm)
-
-
L/min
(gpm)
L/min
(gpm)
L/min
(gpm)
mA
kV
mA
kV
mA
kV
mA
kV
m
(ft)
m/s
(fps)
°C
(°F)
%
of Process Operation
2-1
May 13, 1987
915
(33,2800)
816
(1,500)
866
(1,591)
780
(1,436)
1,010
(1,850)
1,060
(1,940)
980
(1,796)
-2.0
(-0.08)
-8.9
(-0.35)
NA
78
(172)
67 x 106
(63 x 106)
927
(245)
6.7
2.9
322
(85.1)
142
(37.5)
142
(37.5)
23.1
29.5
16.4
31.1
63.3
29.0
74.4
29.2
18.3
(60)
12.5
(41.1)
71
(159)
11.59
Results1 • Test Condition 2
Run No.
2-2
May 14, 1987
914
(31,200)
821
(1,510)
872
(1,602)
781
(1,438)
982
(1,800)
1,020
(1,868)
940
(1,724)
-2.0
(-0.08)
-8.9
(-0.35)
NA
80
(176)
68x106
(64 x 106)
893
(236)
7.5
3.1
322
(85.1)
142
(37.5)
142
(37.5)
14.6
30.0
9.7
30.8
106.0
29.3
111.7
29.0
18.3
(60)
12.3
(40.5)
72
(161)
11.72

2-3 -
May 15, 1987
888
(31 ,400)
804
(1,480)
854
(1,569)
779
(1,434)
954
(1.750)
999
(1,830)
915
(1,679)
-2.0
(-0.08)
-8.9,
(-0.35)
NA
82
(180)
70x106
(67x106)
840
(222)
7.1
2.9
321
(84.8)
142
(37.5)
142 :,
(37.5)
31.8
30.4
18.5
30.5
114.1
28.7
96.5
28.9
18.3
(60)
12.0
(39.4)
71
(160)
10.14
1 Average of readings taken during each run.
2 Approximate IWS inlet temperature.
3 Average of readings from two simultaneous MM5 trains.
4 Orsat analysis.
                                                           48

-------
Table 4-6. Example Incinerator
Parameter
Test date •
Combustion gas flowrate
PCC temperature
Mean
Maximum
Minimum
SCO temperature
Mean
Maximum
Minimum
PCC pressure
SCC pressure
Quench inlet temperature
Quench outlet temperature2
Heat input rate
Quench water flowrate
IWS pH
IWS pH .
Prescrubber water flowrate
2nd stage IWS3 water flowrate
3rd stage IWS4 water flowrate
IWS Unit 2A - DC Current
IWS Unit 2A - DC Voltage
IWS Unit 28 - DC Current
IWS Unit 2B - DC Voltage
IWS Unit 3A - DC Current
IWS Unit 3A - DC Voltage
IWS Unit 3B - DC Current
IWS Unit 3B - DC Voltage
Stack height
Stack exit velocity3
Stack temperature3
Stack excess Og4
Test Case: Summary of
Units
-
Actual m3/min
(acfm)
°C
(°F)
°C
(°F)
°C
<°F)
"C
(°F)
°C
(°F)
°C
(°F)
mm HoO
(in H2O)
mm HgO
(in H2O)
-
°C
(°F)
kJ/hr
(Btu/hr)
Umin
(gpm)
-
-
L/min
(gpm)
L/min
(gpm)
L/min
(9pm)
mA
kV
mA
kV
mA
kV
mA
kV
m
(ft)
m/s
(fps)
"C
(°F)
%
Process Operation
3-1
May 15, 1987
878
(29,400)
793
(1,460)
840
(1,514)
760
(1,400)
971
(1,780)
1,020
(1,868)
960
(1,760)
-2.0
(-0.08)
-8.1
(-0.32)
NA
81
(177)
62 x 106
(59x106)
871
(230)
6.9
3.3
322
(85.1)
142
(37.5)
142
(37.5)
32.B
29.0
21.3
29.5
129.8
25.0
112.5
24.0
18.3
(60)
11.6
(38.1)
72
(161)
10.68
Results1 - Test Condition 3
Run No.
3-2
May 16, 1987
862
(30.400)
802
(1,475)
860
(1,580)
750
(1,382)
954
(1 ,750)
1,024
(1,875)
954
(1,750)
-2.6
(-0.10)
-8.4
(-0.33)
NA
79
(175)
61 x 10s
(58 x 106)
916
(242)
7.0
4.1
321
(84.9)
142
(37.5)
142
(37.6)
23.2
29.5
17.4
29.5
124.2
27.1
103.6
27.0
18.3
(60)
11.8
(38.9)
72
(161)
11.19

3-3
May 16, 1987
869
(30,700)
804
(1,480)
856
(1,573)
744
(1 ,372)
949
(1,740)
1,018
(1,865)
949
(1,740)
-2.6
(-0.10)
-8.6
(-0.34)
NA
77
(171)
63X106
(60x106)
958
(253)
7.3
3.7
322
(85.1)
142
(37.5)
142
(37.5)
14.5
28.7
8.1
29.3
75.4
26.5
66.5
26.8
18.3
(60)
12.0
(39.2)
71
(160)
10.58
1 Average of readings taken during each run.
2 Approximate IWS inlet temperature.
5 Average of readings from two simultaneous MM5 trains.
6 Orsat analysis.

-------
Table 4-7. Example Incinerator Test Case: Summary of Emission Performance Results • Test Condition 1 ;
Run No.
Parameter
Test date
ORE - Trichloroethylene
ORE - Tetrachloroethylene
ORE - Trichlorobenzene
Paniculate matter1
HCI emissions
Cl removal efficiency
Stack gas flowrate2
Stack gas flowrate2
Oxygen3
Carbon monoxide1 -3
Units
-
%
%
%
mg/Normal m3
(gr/dscf)
kg/hr
(Ib/hr)
%
Actual m3/min
(acfm)
Normal m3/min
(acfm)
%
ppm
1-1
May 12, 1987
99.9960
99.9990
99.9950
80.2
(0.0350)
0.560
(1.24)
99.64
875
30,900
507
17,900
10.55
62.0
1-2
May 12, 1987
99.9980
99.9970
99.9998
65.5
(0.0286)
0.831
(1.83)
99.45
892
31 ,500
515
18,200
10.60
29.9
1-3 ' ;i
May 13, 1987
99.9990
99.9991
•--99.9992 '•'•:-•<
32.8
(0.0143)
1.06
(2.33)
99.31
830
29,300
481
17,000
10.81
52.2
  1 Corrected to 7% 02.
  2 Average of readings from two simultaneous MM5 trains.
  3 Concentrations in stack gas from facility in situ monitor. Oxygen monitor used to correct CO readings.
Table 4-8.    Example Incinerator Test Case: Summary of Emission Performance Results - Test Condition 2

                                                                                   Run No.
Parameter
Test date
ORE - Trichloroethylene
ORE • Tetrachloroethylene
ORE - Trichlorobenzene
Paniculate matter1
HCI emissions
Cl removal efficiency
Stack gas flowrate2
Stack gas flowrate2
Oxygen3
Carbon monoxide1.3
Units
-
%
%
%
mg/Normal m3
(gr/dscf)
kg/hr
(Ib/hr)
%
Actual m3/min
(acfm)
Normal m3/min
(acfm)
%
ppm
2-1
May 13, 1987
99.9993
99.9992
99.9930
101.6
(0.0444)
0.217
(0.478)
99.86
878
29,400
518
18,300
11.55
56.3
2-2
May 14, 1987
99.9992
99.9950
99.9960
87.5
(0.0383)
1.39
(3.07)
99.11
864
30,500
510
18,000
11.39
80.1
2-3
May 15, 1987
99.9960
99.9980
99.9991
112.1
(0.0490)
0.319
(0.704)
99.80
841
29,700
496
17,500
10.43
76.5
 1 Corrected to 7% O2-
 2 Average of readings from two simultaneous MM5 trains.
 3 Concentrations in stack gas from facility in situ monitor. Oxygen monitor used to correct CO readings.
                                                            50

-------
Table 4-9. Example Incinerator Test Case: Summary of Emission Performance Results - Test Condition 3
Run No.
Parameter
Test date
ORE - Trichloroethylene
ORE - Tetrachloroethylene
ORE - Trichlorobenzene
Particulate matter1
HCI emissions

Cl removal efficiency
Stack gas flowrate2
Stack gas flowrate2
Oxygen3
Carbon monoxide1-3
Units
-
%
%
%
mg/Normal m3
(gr/dscf)
kg/hr
(Ib/hr)
%
Actual m3/min
(acfm)
Normal m3/min
(acfm)
%
ppm
3-1
May 15, 1987
99.9990
99.9994
99.9950
74.4
(0.0325)
1.61
(3.54)
98.93
813
28,700
484
17,100
10.76
63.9
3-2
May 16, 1987
99.9950
99.9980
99.9950
55.3
(0.0242)
0.702
(1.55)
99.53
830
29,300
493
17,400
11.34
66.3
3-3
May 16, 1987
99.9970
99.9980
99.9993
96.4
(0.0421)
1.55
(3.42)
99.02
838
29,600
498
17,600
10.70
90.0
          1 Corrected to 7% Oz.
          2 Average of readings from two simultaneous MM5 trains.
          3 Concentrations in stack gas from facility in situ monitor. Oxygen monitor used to correct CO readings.
        The universal strategy sets the values for the control
        parameters in the following order:

        1. Control parameters from  trial burn  data  that are
           related to waste destruction

        2. Control parameters from  trial burn  data  that are
           related to APCE performance

        3. Control parameters that are independent of trial
           burn data
        The  results of the trial  burn  for the test case have
        been summarized  in Tables 4-4 through 4-9 and  in
        Appendix G. The guidelines of Chapter 2 may now be
        used to set control parameter limits  based on these
        data. The  trial burn  was  performed at three  test
        conditions  (or nominal  operating points) with three
        runs performed at each test condition. Following the
        guidelines of Chapter 2, operating conditions  of the
        three runs were averaged to yield a composite set  of
        conditions for each test.  The composite results, which
        are  summarized  in  Table  4-10,  show  that  the
        incinerator  was in  compliance  with  performance
        standards for each run of all three  test conditions.
        The  permit conditions  chosen are  summarized  in
        Table  4-11 and  are  discussed  in  detail  in  the
        following sections.
   4.4.1  Control  Parameters  Related to  Waste
   Destruction
   The control parameters related to waste destruction
   are listed in Table 3-2. The values of the parameters
   as they are to be specified in the permit are shown in
   Table  4-11.  Following the recommended  practice,
   the group A parameters listed below are the first to be
   set.
   •  Minimum temperature at the kiln and  SCC exits
   •  Maximum CO emissions
   •  Maximum flue gas flowrate at the stack
   •  Maximum pressure in the kiln and SCC
   •  Maximum feed rates:
      -  of  each waste stream  to  each combustion
        chamber
      -  of combined waste streams  to all combustion
        chambers
      -  per container,  maximum size of  containerized
        waste

   As  shown  in  Table  4-6,  the  mean kiln temperature
   for each of the three runs under these test conditions
   ranged  from  793 to  8048C (1,460 to 1,480°F).  The
   SCC temperature ranged from 949 C to 971 °C (1,740
   to 1780°F). The variation of the temperatures for all
   the runs is not given here; it  is,  however,  given for
   run  1-1  in Appendix G, Table G-4 and Figure G-
   1. Table G-4 gives  the per minute output from the
k
51

-------
Table 4-10. Average Trial Bum Results At Three Test Conditions
Test Condition
PCC exit temperature, °C
SCC exit temperature, °C
Stack exit velocity, m/s @ 72°C
m/s @ STP
ORE - Trichloroethylene, %
ORE - Tetrachloroethylene, %
ORE - Trichlorobenzene, %
Cl removal efficiency, %
Carbon monoxide1, ppm
Feed rates, kg/min
Drummed waste (Si)
Sludge (SL)
PCC organic waste (L2)
SCC otganic waste (L4)
Wastewater (L1)
Total PCC waste
Total SCC waste
Tolal inorganic ash
Total halides
APCE inlet temperature, °C
Voltage to IWS, kV
Total electrical power to !WSs, kVA
IWS blowdown rate, L/min
Particulate concentration, mg/dscm
IWS water flowrate, L/min
pH to IWS
Permit Target
800
950
12.3
10.4
99.99
99.99
99.99
99
100

27
9
2.3
6.0
31
69
6
13.8
2.3
80
30
7.0
15
180
650
7.0
1
914
1,040
12.3
10.4
99.998
99,998
99.998
99.47
48.0

27
8.4
2.2
5.9
30
73
5.9
13.8
2.5
78
29.6
7.04
17
59.5
606
6.6
Test No.
2
814
932
12.3
10.4
99.998
99.997
99.996
99.59
71.0

29
7.8
2.3
6.0
31
73
6
14.4
2.6
80
29.7
6.63
20
100.4
606
7.1

3
800
958
11.8
.. . .,. 10.Q
99.997
99.998
99.996
99.16
80.1

27
7,8
2.3
.6.0
29
69
6
13.8
2.5
' 79 ' .
27.7
6.44
15
75.4
606
7.1
 " Corrected to 7% O2.
temperature  data  logger;  and  Figure  G-1  is the
graphical representation.

Table 4-10  summarizes  the  mean  operating
conditions during each of the successful tests. Note
that  all these values are  given in metric units;
however,  permit conditions  should normally  be
reported in  the  units in  which  the  monitoring
equipment is calibrated. For temperature, the mean is
simply the  average  of the  mean temperatures  at
which the kiln and  SCC operated during each of the
three runs  at  each  condition, e.g., the mean of the
time-averaged temperatures for  each of the three
runs. The  lowest  kiln temperature  was  800°C
(1,470°F) during test 3, while the lowest mean SCC
temperature was 932°C (1,710°F) during test 2.  The
minimum  temperature permit  condition could  be
based on either test 2 or test 3. It is recommended
that the SCC and PCC minimum temperatures not be
taken from  different tests. While in this case  the
differences are inconsequential, they are interrelated,
and a temperature  for each  based on the results  of
different tests  could  result  in  incompatible  limits.
Table 4-12  summarizes the pertinent results  of the
tests for making the  decision.

The  following  calculation can be used  to  estimate
whether test 2 or 3  have significantly lower SCC gas
residence times. To do this,  the gas flowrate (in this
case represented by the gas velocity at the stack at
standard conditions) is converted to the respective
temperatures of the  SCC. For example:

          10.4 x (932 +  273) / 293 = 42.8


The gas velocities are proportional to the actual gas
volumetric flowrate; hence, they are the inverse of the
residence time  in the SCC.  Thus, we can  say that
test 3 was run at a slightly longer residence time than
test 2.  Because in this case test 2 shows  the shorter
residence time  by a trivial  amount  and lower SCC
temperature,  it  should be  used to set the limit on
temperature;  however,  the  two  conditions  are  so
slightly different that either could be used with little or
no risk.


The next control parameter that needs to be set is the
CO emissions. As indicated in Section 2.1.2, the EPA
is  presently  developing  guidelines   for  these
emissions. The CO for the nine runs performed varied
between 29.9 to  90.0 ppm,  corrected to 7 percent
oxygen. As a result,  under the present guidelines, the
limit should be set at 90 ppm, the highest measured
during  test number 3. Under the new guidelines, the
                                                 52

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Table 4-11.  Summary of Permit Limits for Incinerator Example Test Case
Parameter
PCC waste cutoff temperature, °C
SCO waste cutoff temperature, °C
Maximum stack velocity, m/s
Maximum feed rates, kg/min
PCC solid waste (S1 & S2)
PCC sludge (SL)
PCC organic liquid (L2-L5)
SCC organic liquid (L2-L5)
PCC wastewater (L1 )
Total PCC waste
Total SCC waste
Total inorganic ash
Total halides
Maximum size waste drum, m3
Minimum IWS voltage, kV
Minimum scrubber blowdown, L/min
Minimum scrubber water flow, L/min
Minimum pH to scrubber
Maximum CO, ppm {1 -hr average)
Maximum kiln cutoff pressure
Maximum heat input rate, kJ/hr
Maximum SCC waste viscosity, cp
Maximum SCC waste turndown ratio
Minimum SCC waste burner pressure, N/m2
Minimum SCC waste HHV, kJ/kg
Maximum APCE inlet temperature, °C
Target
800
950
12.3
27
9
2.28
6
30
69
6
22.8
2.28
0.17
30
15
650
7.0
-
_
-
-
-
-
80
Limit
800
960
12.3
288
7.8
2.34
6
28.8
73.2
6
14.4
2.64
. 0.17
29.7
15
606
7.1
100
Atmospheric
63 x 106
100
8:1
310,000
11,600
80
Test
Condition
3
3
1,2
2
2
2,3
3
2
2,3
2
2
1,2,3
2
3
2
2
-
m
-
-
-
-
2
Justification
Minimum measured
Minimum measured
Equation 7
Maximum measured
Minimum temperature condition
Maximum measured
Maximum measured
Minimum temperature condition
Maximum measured
Maximum measured
Maximum stack velocity condition
Maximum stack velocity condition
Only trial burn setting
Maximum stack velocity condition
Equation 9
Maximum stack velocity condition
Maximum stack velocity condition
Per CO guidelines
Manufacturer specification
Maximum measured
Manufacturer specification
Manufacturer specification
Manufacturer specification
Manufacturer specification
Maximum measured
Table 4-12   Data Used for Setting Temperature Limit
	-  • .  .	  Test 2       Test3
 PCC temperature, °C             814         800
 SCC temperature, °C             932         958
 Combustion gas velocity, m/s
 At stack conditions   .            12.3         11.8
 AtSTP  :  "...                   10.4         10.0
 At SCC temperature              42.8         42.0


limit should be set  at 100 ppm, because 100 ppm CO
is generally considered to be the  range for proper
operation of the incinerator which  would minimize the
risk of excessive PIC formation and POHC emissions.

The next operating parameter that needs to be set is
the  maximum  flue  gas  velocity or  flowrate.  As
discussed  in Section  2.1.3, flowrate  should  be
measured as close to the exit of the SCC as possible;
however, in most cases, the gas  velocity at the inlet
to the stack  is an adequate indicator of combustion
gas velocity. It was used in this case and found to be
adequate.,  By  the careful selection  of  the test
conditions,  the maximum combustion gas flowrate (by
whatever measurement method  decided on)  should
be  specified from  the  same  test  as  was  the
temperature,  whenever  possible.  In  this  case,  the
maximum gas flowrate  when corrected to SCC
conditions was very slightly lower in test 3 than in test
1 or 2.  It was the same during test  1 and 2. If the
results of test 2 are used  to  specify the maximum
combustion gas flowrate,  all the criteria are satisfied,
i.e.,  maximum measured during a test  and  chosen
from the  same  test  as  the  minimum SCC
temperature.

For  illustration, however, assume that the  results
require interpolation of data and  that equation  7 of
Section  3.6.1 will be used to implement the universal
strategy.  If  the temperature  and combustion  gas
flowrate limit were  set on the basis of test 3  instead
of test 2, the maximum  gas  velocity that would be
allowed  is 11.8 m/s  (38.7 fps). This limit could be
unduly restrictive;  for example,  when a  high  heat
value waste  is burned, the temperature  will increase
above the minimum,  (which  by itself is acceptable),
but the  gas  velocity  would  also increase  above the
11.8-m/s (38.7-fps) maximum  and trigger a waste
cutoff. Under these very  narrow circumstances,  it is
possible  to  use  equation  7  of  Section 3.6.1 to
determine whether the higher gas velocity of  tests 1
and  2 can  still achieve  the  ORE under the lower
                                                  53

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 temperature of test 3. It is worth repeating that in the
 example  case, the  exercise  is  trivial  since  the
 difference  between  the  two sets  of  conditions is
 negligible. It is presented here for illustration.

 The residence  time (or gas flowrate) that is required
 to  achieve  99.99  percent ORE at  the  lower
 temperature conditions  can  be  estimated  from
 equation 7 of Section 3.6.1.  As  the trichlorobenzene
 had the lowest  average ORE of 99.996 percent at this
 minimum  temperature  test condition, its  results can
 be used  for the  purpose.  By  equation 7, for this
 compound, then,
                     99.996% \
    stack max
                    -9.21
                                11.8m/s=13.0m/s
The value of 13.0 m/s (42.6 fps) is greater than the
12.3 m/s (40.3 fps) that was measured at the higher
temperatures; hence, the maximum gas  velocity  in
the stack can safely be set at  12.3 m/s  (40.3 fps).
Had the value calculated by equation 7  been less
than  12.3  m/s  (40.3  fps)  (the  highest  velocity
measured),  the lower, calculated velocity would have
been used.  However, the applicant  can design the
test in most cases to achieve minimum temperature
and maximum gas flowrates by the addition of water
to the PCC  or by the use of  waste blending. Although
this example was used  to demonstrate the universal
approach, the permit conditions could be set using a
multiple  point permitting  strategy,  i.e.,  different
temperatures and velocities for different combinations
of waste feeds.

The next parameter to  be set  is  the  maximum
pressure in  the kiln and SCC. During the tests, both
the  kiln and SCC pressures were  constant during
each run. As Tables  4-4 through  4-6  show,  the
pressure differences  among runs were  modest  as
well. Although not shown in the results, no  indications
of puffing  were observed during  the trial burns. As a
result,  following  the  guidelines in Section  2.1.4, the
minimum  operating pressure set-point for both  the
kiln and the SCC is atmospheric pressure,  with the
caveat that the SCC pressure must be lower than that
in the PCC at all times.

According to the guidelines of Chapters 2 and 3, the
maximum  feed rates of low heating value  wastes
should be taken from the  minimum temperature test
condition. The wastewater (with no heating value) and
the high-moisture sludge  (with  a  heating  value  of
6,200 kJ/kg  [2,700 Btu/lb]) may  be classified as low
heating value  wastes.  The permit  limits  for the
maximum  feed rates for these waste streams could
be taken from either test 2 or 3. In this case, it was
taken from test condition 2  for consistency  with the
temperature  selection. From  Table 4-10, the permit
 limit for maximum sludge feed rate should be set at
 7.8  kg/min (1,030 Ib/hr),  and the permit  limit  for
 maximum wastewater feed rate should be set at 28.8
 kg/min  (3,800 Ib/hr).

 The maximum feed  rates of medium-  and  high-
 heating  value waste streams  should  be taken from
 the test condition at which each individual feed rate is
 maximized. Thus, from Table  4-10, the permit limits
 for maximum feed rates should be 28.8 kg/min (3,800
 Ib/hr) for the solid waste, 2.3 kg/min (300 Ib/hr) for the
 12 liquid waste, and 6 kg/min (790 Ib/hr) for the L4
 liquid waste. All these  feed rates meet or exceed the
 permit limit targets.

 The permit limit  for the combined feed  rates of all
 wastes  to each combustion chamber should be taken
 from  the  test condition  at  which  that  value  is
 maximized  for  each  chamber.  In  this  case,  the
 combined  feed  rate of all  wastes  to the kiln was
 maximized  at 73.2 kg/min (9,660  Ib/hr)  in test
 condition 2, and the combined  feed rate of all wastes
 to the SCC was maximized at  6 kg/min (790 Ib/hr)  in
 test condition 2. Those values should be taken as the
 permit limits.

 Only one size of containerized  waste was fired in the
 trial  burn:  208-L (55-gal)  drums.  Thus,  the permit
 limit  for the maximum size of containerized  waste
 fired to  the kiln should be set at  208 L. This waste
 was fired at a rate of one drum every 6 minutes. This
 value should  also be  incorporated into  the permit
 condition.

 4.4.2  APCE-Related  Parameters
 Permit limits for parameters set from  trial burn data
 that are related to APCE performance should be set
 according to the guidelines of  Section 3.6.2. For this
 example test case, these parameters include:

 •  Maximum ash feed rate to the incinerator system

 •  Minimum kV settings to IWS
 •  Minimum paniculate  scrubber blowdown rate

 •  Maximum total  chloride feed rate to the  incinerator
   system
 •  Minimum L/G ratio to the absorber

•  Minimum pH to the absorber
•  Maximum APCE inlet gas temperature

The maximum  ash feed rate should be taken from the
maximum stack gas velocity data point that occurred
at test  conditions  1 and 2. The ash  feed rate was
highest  at test condition  2 at 14.4  kg/min  (1,890
Ib/hr), which exceeds  the permit  limit  target.  This
value should be set as the  limit.

The minimum  kV setting to the IWSs (taken as the
sum of the electrical power to all scrubbers) was 27.7
                                                 54

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kV, taken at test condition 3. However, because the
ash feed rate at condition 2 is actually higher than the
ash  feed rate at test  condition 3  and  the stack
velocity at that condition is also higher than that of
test  condition 3, the maximum setting of 29.7 KV
measured at condition 2 should be set as the permit
limit for minimum KV to the IWSs.

The  minimum particulate scrubber blowdown rate of
15 L/min (4 gpm) was  achieved at test condition 3.
Because the  maximum  ash feed rate and maximum
stack velocity  were  recorded  at test condition  2,
equation  9 must  be  satisfied to  justify  setting
minimum  blowdown  from  a nominal operating  point
other than test condition  2. From  Table 4-10, the
ash feed rate  and stack velocity at  test condition  2
were  14.4 kg/min (1,900  Ib/hr) and  12.3 m/s  (40.3
fps), respectively. At test condition 3,  the ash feed
rate  was 13.8  kg/min (1,820 Ib/hr), the  stack velocity
was  11.8  m/s   (38.7 fps),  and  the  particle
concentration was 75.4 mg/dscm. Because velocity is
equal to  gas  flowrate  divided by  cross-sectional
area, equation 9 can be  solved:
                      13.8 kg/min
     75.4 mg/dscm

      180 mg/dscm
   stack
                      14.4 kg/min
12.3
                                      stack
                   0.42 <, 0.88
where the cross-sectional area of the stack (Astack)
cancels  out.  The  equation  is  satisfied;  so  the
minimum scrubber blowdown rate permit limit can be
taken from test condition 3 at 15 L/min (4 gpm).

According to  the  guidelines of Section 3.6.2,  the
permit  limits for  maximum  total halide feed rate,
minimum water  flowrate,  and minimum  pH to  the
absorber (in this case, the scrubber system) should
all be set from  the  maximum  flue  gas flowrate, or
stack velocity, operating condition. Extreme values of
these parameters were not all  achieved  at the same
test condition. However, in test condition 1 where the
stack velocity  was at a maximum, all values  satisfied
the permit limit targets. Thus, the permit  limits should
be taken from test condition 1 at 2.52  kg/min (332
Ib/hr) maximum total halide feed rate, 606 L/min (160
gpm)  minimum  scrubber water  flowrate,  and  6.6
minimum pH to the scrubbers.

The  maximum APCE  inlet  temperature (same as
quench  outlet  temperature) was 80 °C (176°F) during
test 2.  Therefore,  the  maximum APCE  temperature
will be set at 80°C  (176°F) which  is less  than  the
manufacturers specification of 100°C (212°F).

4.4.3 Parameters Independent of Trial  Burn Data
Permit parameters for the example test case that are
independent of the trial burn include:
•  Maximum  total  heat  input capacity  for each
   chamber

•  Maximum viscosity of liquid waste to the SCC

•  Maximum SCC liquid waste turndown

•  Minimum SCC atomization fluid pressure

•  Minimum  SCC  waste  heating  value (when no
   auxiliary fuel is fired)

The permit  parameters listed  above should  be set
according  to  the  recommendations   of the
manufacturer.  For this system, the  kiln should be
maintained at negative pressure; the maximum total
heat input to the kiln is 20,000 kJ  (19,000 Btu)/s; the
maximum total heat input to  the  SCC  is 11,700 kJ
(11,000 Btu)/s; the maximum viscosity of liquid waste
to  the SCC is 100 cp;  the maximum turndown for the
liquid waste to the SCC is  8:1, which  results in  a
liquid waste flowrate range of 0.06 to 0.45 kg/min (8
to  60 Ib/hr)  to each of the  two waste burners; the
minimum  atomization  fluid  pressure for the  liquid
waste  SCC is  310,000  N/m2  (45 psig);  and  the
minimum SCC waste heating value in the absence of
auxiliary fuel is 11,600  kJ/kg (5,000 Btu/lb).

4.4.4 Summary of Operating Limits
The permit writer  and  especially the permit  applicant
should have a clear understanding of the interrelated
effects of the operating limits imposed by a proposed
set of permit conditions. This is particularly important
during the trial burn planning  stage when the permit
applicant has  the opportunity  to examine the
consequences of the  permit conditions that  would
result from the trial burn and to modify the  plan
accordingly.  Before agreeing  to a  set of limits,  the
operator  is encouraged to perform energy and mass
balance  calculations such  as  those described  in
Appendix E to verify that the  permit conditions  are
internally consistent. As  an  example,  energy and
mass balance  calculations  have  been  used to
establish  the  operating  envelope for the  rotary
kiln/SCC incinerator of the example test case to meet
the following set of permit conditions as established
by the trial burn:

•  Minimum kiln temperature:  800°C (1,470°F)

•  Minimum SCC temperature: 950 °C (1,750°F)

•  Maximum stack velocity: 12.3 m/s (40 fps)

•  Maximum waste feed rates
   -  Kiln solid waste: 27 kg/min (3,600 Ib/hr)
   -  Kiln sludge: 9 kg/min (1,200 Ib/hr)
   -  Kiln wastewater: 30 kg/min (4,000 Ib/hr)
   -  Kiln liquid organic waste: 2.28 kg/min (300 Ib/hr)
   -  SCC liquid organic waste: 6 kg/min (800 Ib/hr)
                                                 55

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•  Maximum total halides feed rate: 2.28 kg/min (300
   Ib/hr)
•  Maximum total ash  feed  rate:  13.8  kg/min  (1,800
   Ib/hr)
•  Minimum water  flowrate  to  absorber:  650 L/min
   (170 gpm)
•  Minimum pH to absorber:  7.0
•  Minimum KV settings to IWSs: 30 KV
•  Maximum size of containerized waste to PCC: 208
   L (55 gal)

A  complete operating envelope  for this system would
involve calculation  of the  interrelated  effects of
variations in those  parameters  that the  operator can
control, i.e., waste,  fuel and  air feed  rates  and
variations  in those parameters  that  the operator
cannot control such as waste composition. While an
energy and mass balance could be used to develop a
complete  operating  envelope,  a  large  number of
calculations would  be  involved, and the  resulting n-
dimensional (where  n is  the number of variables)
operating  envelope  would be difficult to present and
interpret.  For most systems, it is not necessary or
desirable to investigate the effects of variations in all
parameters simultaneously.

An energy and  mass  balance  can be useful  to the
operator to achieve the following:

1.  Predict operating  conditions for new incinerators

2.  Verify  trial burn  temperature  and combustion  gas
   velocity  targets  for  existing  facilities  and specific
   trial burn feed compositions

3.  Check that all feeds can be maximized in one test,
   and  verify that temperatures  and combustion  gas
   velocity will be the  same for any two tests to  be
   used in obtaining  one set of conditions.

To illustrate the value of energy  and mass balance
calculations, the operating   envelope  for the test
example was developed for the following constraints:

•  The  feed rate of  only one waste stream at a time
   was  allowed  to  vary. All  other waste  feed rates
   were assumed to be constant at their permit limits.

•  Waste compositions  were  assumed to be constant.

•  The  primary air flow was  assumed to be constant
   at 480 kg/min  (63,400 Ib/hr).

•  The  SCC was assumed to operate at 20 percent
   local excess air.
 Under these constraints, the controlling permit limits
 were the combustion chamber exit temperatures,  the
 waste feed rates, and the flue  gas flowrate.  Figure
 4-2 shows the effect of varying the feed rate of each
 waste stream about the baseline on the total auxiliary
 fuel  (combined natural gas flow to the  kiln and  the
 SCC) required to maintain operation within the  permit
 limits. The  splid lines in the  figure' represent  the
 operating limit imposed by maintaining the kiln  or  the
 SCC  at the minimum temperature, the dotted lines
 represent the maximum  waste  feed  rate  limit,  the
 dashed lines represent the maximum flue gas flowrate
 limit,   and  the  dash-dotted  lines  represent  the
 physical limit of zero  waste flow.       ...-•,;

 Allowing for fluctuations, it is most economical  (i.e., it
 requires the least auxiliary fuel) to run as close to  the
 minimum  temperature line as  possible.  The   liquid
 wastes and the drummed waste have  sufficient
 heating values so that a reduction in waste flow rnust
 be  offset by an increase  in  auxiliary fuel flow to
 maintain  minimum temperature.  Because the sludge
 heating value is barely  sufficient  to  maintain  the
 minimum kiln temperature, a reduction in  sludge flow
 has little effect on the fuel flow  required  to maintain
 temperature. The wastewater has  no  heating  value,
 so  a  reduction  in  wastewater flow  reduces the
 auxiliary fuel requirement.

 In all cases, as the auxiliary fuel flowrate is increased
 above the  minimum temperature operating  line,
 temperatures rise and the flue gas flowrate increases.
 The upper  limit on auxiliary fuel flow is imposed  by
 the maximum  permitted flue  gas flowrate.  In  many
 cases, this limit is academic because economics and
 equipment  temperature  limitations  will prevent the
 operator from reaching these limits.

 These  conclusions are  valid only  under  the
 constraints  for  which the operating envelope was
 developed.  For instance,  if  primary air  flow  were
 allowed to vary,  the  maximum flue gas flowrate limit
 may  become   more important.  If  the  waste
 compositions varied,  the maximum halide  and ash
feed rates  may become more  restrictive  than the
 maximum feed rate of each waste stream. Therefore,
 in developing an operating envelope, it is important to
consider the system  involved and set the constraints
accordingly.  Because the permit applicant  best
understands the system and how it is to be operated,
it is recommended that calculations of this nature  be
performed by the permit applicant during the trial burn
planning  stage  and  prior to  accepting permit
conditions to ensure that all parameters  required can,
in fact, be achieved.
                                                 56

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Figure 4-2.   Operating envelope for example test case.
        30001- r
        2000
   o
        1000
i r
                                                                       Baseline Flows (Ib/h*
                                                                       Drummed Waste
                                                                       Sludge
                                                                       Waste Water
                                                                       Kiln Liquid
                                                                       Afterburner Liquid
                                                                       Primary Air
                                                                3,600
                                                                1,200
                                                                4,000
                                                                 300
                                                                 800
                                                               63,700
               0  1000 2000 3000   0   500  1000  0     2000   4000 0 100  200 300   0
                  Drummed Waste         Sludge         Waste Water         Kiln Liquid

                                    Variations of Individual Waste Flows About Baseline (Ib/h)*
                                                              400
                                                            SCC
  800
Liquid
                                                       57

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                                              CHAPTERS
                                           Data Reporting
The review of  relevant permit information  is often
complicated by  the lack of uniformity in content  and
format of  the data  submitted. Required  information
may be either missing or buried in a trial  burn report
in an inappropriate location.  Furthermore, redundant
or irrelevant information in the  report may also delay
the review and permit writing process.

The following are typical problems that  the permit
reviewer/writer may encounter:

•  It is  not always  clear which  data  are used to
   calculate the results.

•  Treatment of  analytical, sampling, and field blank
   corrections is  not uniform.

•  Not all relevant operating conditions are reported.

•  Departures  from standard sampling  and  analysis
   methods are not well documented.

•  Some analytical results do not appear in the report.

•  Quality  assurance data are inadequate.

•  Significant departures have  been taken from  the
   trial burn  plan, which may have  been   written
   several months before the trial burn.

Clearly,  there is  a need for uniformity in kind, extent,
and organization of the  trial  burn information so  that
the permit writer's task  is  facilitated. The entire
permitting process would be speeded up, and  soundly
demonstrated  technology to  treat  hazardous waste
would be  made  available  to serve  the  needs of  the
regulatory agency, the facility, and the public.

Reports of certain  performance  results  and  other
information resulting from trial burns are mandated by
the regulations.  Other  information  is  needed to
support  the performance results and indicate facility
operations, while additional information  is needed to
ensure the integrity of the results and confirm  that the
protocol agreed  upon was adhered to. In the past,
because  this  assortment  of test  results  and
supporting  data has been presented in  a wide variety
of formats and  units, it  has  been difficult  for  the
permit writer to rapidly assess  or compare trial burn
results.

There are several types of reporting needs. First,  the
permit writer needs the  results of performance and
operation tests  during the trial  burn  itself.  Second,
design data are also required for engineering analysis
in support of permit conditions. Finally, both design
data  and performance results  are needed as  input
into  the national data  base for  hazardous  waste
treatment, the  HWCTDB, under development by  the
EPA and the Department of Energy (DOE), Trial burn
data  presented  in a consistent format will  facilitate
entry of the results into the HWCTDB.

It  is difficult and unnecessary  to  develop a single,
uniform  reporting  format  that will  apply to  all
situations. However, the format given below should
be applicable to most trial burns, and the applicant is
urged to follow  it as closely as is practical.

Example reporting forms  to be followed as closely as
is  feasible  are  included  in Appendix F. An example
trial burn report format is provided  in  Section 5.2.  To
follow  the  example  format and use  the appended
forms should alleviate many of the  problems cited. In
addition, an example trial burn  report  of a test case
has been provided in Chapter 4 as a  guide to using
the format and forms.


5.1 Design Data Reporting
Basic  design information is  required  in  the permit
application  according  to  regulations  in  40  CFR
270.62.  To produce  a  complete,  stand-alone
document,  the  permit applicant  should insert in the
trial  burn report a  summary of the   major  design
criteria  of  the  incineration facility including  basic
design information  and  key  operating parameters.
Reviewers can  then compare the test  conditions with
the original  design  criteria without reference to the
original permit application. Furthermore, as discussed
in  Chapter 2, group  D permit parameters reflect limits
on operation based  on equipment design information
and manufacturer specifications. These design data
should be made available to the  permit writer for rapid
evaluation of necessary permit limits.  In some cases,
additional design information can  be  requested  for
                                                  59

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 computer modeling  of  the test  results  using  the
 energy  and mass balance model  mentioned above.
 Following is an example of the design information that
 should be listed in a trial burn report:

 •  Type of incinerator (i.e., liquid injection, kiln)

 •  Linear dimensions of  the incineration unit including
   the cross-sectional  area of each  combustion
   chamber

 •  Heat capacity of each combustion chamber

 •  Type(s) of waste feed systems

 Additional design  information should be provided for
 the following equipment:

 •  Liquid  waste burner  type(s) and  capacity and
   design  specifications  for  viscosity  of  feed,
   suspended  solids,  atomization  requirements,
   turndown, and waste heating value
 •  Forced and  induced draft fan capacities
 •  Auxiliary  fuel  type  and capacity for  each
   combustion  chamber
 •  Design pressures  and  pressure  drops  for the
   combustion  chambers and  other  gas  handling
   equipment

 •  APCE
   -  Maximum design and inlet temperature
   -  Gas handling capacity
   -  Pressure  drop
   -  Liquor  (water) feed  rate capacities
   -  ESP or IWS electrical requirements
   -  Other parameters which affect  performance

 A sample  reporting format is shown  in Appendix F. As
 noted, most of the  summary design  information  is
 needed  to  support  the  energy and  mass balance
 model and set  permit limits for group C  parameters.

 Calculations of the design range of  gaseous retention
 time  in  each  combustion chamber  may  also  be
 requested by the permit writer.


 5.2 Trial Burn  Result Reporting
 The requirements for reporting various  types of trial
 burn  data are indicated  in  Tables 5-1  and 5-2.
 Several levels of requirements are shown:

 a.  Required  by regulation
 b.  Recommended  by this guidance handbook or  by
   EPA policy
 c.  Needed for energy and mass balance model
d.  Standard practice/highly recommended
e.  Recommended
f.  Optional
 Data that are required by regulation certainly must be
 reported. Other information may be called for by EPA
 policy  statements, and this, too, may be required by
 the  permit writer on  a case-by-case  basis  through
 use of 270.62(b)(3) or (b)(6)(x).  Other information
 may not have been  required  in  the past  but  is
 necessary for  developing permit  conditions or
 performing  an energy and mass balance as discussed
 in this  guidance handbook. In addition, a large volume
 of the trial burn report consists of information reported
 by standard practice  or  convention and should be
 reported.  Some  information   designated  as
 "recommended"  may not have  been  typically
 reported in  the past, but this type information is highly
 recommended to facilitate the  review. Results that
 may have  some value to the permit writer  also are
 designated  as "recommended."  Finally, other results
 are optional in most situations and may be  included
 for good documentation or in  anticipation  of future
 regulations.

 In   any   event,  "highly   recommended,"
 "recommended,"  and  optional  data to be  reported
 must be agreed  upon prior to the  trial burn  and
 included in  the trial  burn plan so that provisions can
 be made to acquire and report the data.

 Reporting  requirements  and informational needs
 discussed  in  this  handbook are  based  on  EPA
 regulations, policy or  practice.  However,  State or
 other  regulatory agencies  may  have additional
 reporting requirements  that  are  more  stringent than
 the Federal requirements.

 Regulations for hazardous waste incinerator permits
 are found  in  40  CFR 270.62.  Specific information
 currently required in the trial burn report is covered in
 270.62(b)(6) to 270.62(b)(9) and is listed below:

 •  A quantitative  analysis  of the trial  POHCs in the
   waste feed to the  incinerator

 •  A quantitative  analysis of the  exhaust gas for the
   concentration  and mass emissions of  the trial
   POHCs,  O2, and HCI

 •  A quantitative  analysis of the scrubber  water (if
   any), ash  residues,  and other residues  for
   estimating the fate of the trial POHCs

•  A computation  of ORE

•  If the HCI emission rate exceeds 1.8  kg (4 lb)/hr of
   HCI, a computation of HCI removal efficiency

•  A computation  of particulate emissions

•  An identification  of  sources of fugitive emissions
   and means of their control
                                                60

-------
         Table 5-1.    Trial-Burn  Reporting Format and Requirements - Main Report
                                                                                                                            Reporting Requirements1
                                                                                               Incinerator Type
                                                                                 Air Pollution Control Equipment
          Recommended Report Organization
             Specific Information
LFI
RKI
Q
V      PT    IWS    ME     CY     DS    BH    ESP
en
          Preliminary
          Preface

          Table of contents/tables and figures
          1.0 Summary of Test Results
              1.1   Process operation
              1.2  Emissions performance
              1.3  Metals
          2.0 Introduction
              2.1  Background
              2.2  Non-standsard
                   practices/events
          3.0 Performance Results
              3.1 POHCs
              3.2 Chlorine
              3.3 Paniculate
          4.0 Process Operating Conditions
              4.1 Process Overview
R,P
P
R,P
+v
R
• +.F2
R.P
R.P
R.P
R.P
R.P
R
R.P
P
R.P
-t-
R
+ +.F2
R.P
R.P
R,P
R.P
R,P
R
Certification letter
Facility name/location        ,
Name of company performing testing
Test dates                                     t -t- ,F2   + + ,p2
Residence times                                 *       • +
Combustion temperatures
High input (firing) rate
Summary of APCE parameters
Stack height
Stack exit velocity
Stack temperature
Stack excess 02
Test dates
DREs
Particulate emissions
HCI emissions
Cl REs
Stack gas flowrates
02
CO2                                           +        +
CO                                           R,P     R,P


Brief discussion of incinerator type                 +        +       -
Design data summary                           M,F     M,F     M,F
Objective for trial burn                           + +     + +
Planned test matrix and deviations                + +     + •*•
Description of wastes/fuels                       + +     + +
Description of any unusual test methodologoies     + +     + +
Discussion of any special problems encountered    + +     + +

Input rates                                     R,P,F     R,P,F
Emission rates                                  R,P,F     R,P,F
DREs                                          R.P.F     R.P.F
Input rates                                     R.P.F     R,P,F
Emission rates                                  R,P,F     R,P,F
REs                                           R.P.F     R,P,F
Concentrations                                 R,P,F     R,P,F

Brief description                                + +     + +
Process diagram                                + +     + +
Summary of process monitors                    + +     + +
                                                                                                                                M,F

-------
        Table 5-1.    Trial-Burn Reporting Format and Requirements - Main Report (continued)
                                                                                                                   Reporting Requirements1
Incinerator Type
Recommended Report Organization
4.2 Incinerator Operating Conditions
• Combustion temperature

• Waste feed/auxiliary fuel data



• Waste burner data

• Airflow data




• Residue generation rates

• Other operating


Specific Information

PCC Temperature
SCC Temperature
Brief description/firing locations
Feedrates
Firing rates (heat release)
Ash loading rates
PCC atomization/burner pressures
SCC atomization/burner pressures
Flow rates/velocities from MM5
Flow rates/velocity indications from process
monitors
Blower data
Draft measurements
Bottom ash
Fly ash
Scrubber mud/solid residue
Kiln rotational speed
Other conditions deemed important
LFI

R.P.F .
R.P.F
+ +.P
R.P.M
P
P.F
=
P.F
+
R.P.F

+ ,M
R.P.F
-
-
-
-
O
RKI Q

R.P.F
R.P.F
+ +,P
R.P.M
P
P.F
=
P.F
+
R.P.F

+ ,M
R.P.F
M
-
-
+ +
O
Air Pollution Control Equipment
V PT IWS ME CY DS BH ESP

.
.
.
.
.
.......
.
......
.
.

.
.
.
+ -00
o - - - + - -
-
-
             4.3 APCE Operating Conditions
                • Wet process
O)
ro
- Quench


- Venturi scrubber


- Packed tower scrubber
(adsorber)


- Ionized wet scrubber/wet
ESP



- Mist eliminator
• Dry processes
- Cyclone
- Dry scrubber



- Baghouse

:..:•. .J::. - ESP; .-•'. : '


Inlet temperature
Exit temperature
Water flowrate
Inlet temperature
Pressure drop
Water/liquor flowrate
Inlet temperature
Pressure drop
Liquor flowrate
Influent pH
Inlet temperature
Voltage (AC, DC)
Current (AC, DC)
Sparking rate
Water flowrate
Pressure drop
-
Pressure drop
Reagent flowrate
Atomizer rotational speed or nozzle pressure
InleVexit temperatures
Inlet temperature
Pressure drop
Inlet temperature
Voltage -
Current -
Sparking rate
. P.F --------
+ +.
+ +.
P.F .....
P.F -------
+ + -
P.F 	
+ + . . .
P,F 	
P,F - - - -
p.F .....
P.F
P.F 	
. . . + +
•V -----
+ +
.
+ +
+ •!•-
+ +
+ +
P,F
	 P,F
.- . ' - ...... - - - ... - - . P,F
. . .: - . .. • . . p.F
- ; .. - • -••- - •..-.-.": ;; , . . pf
, - - .... - - - - .. •+.+

-------
         Table 5-1.   Trial-Burn Reporting Format and Requirements - Main Report (continued)
                                                                                                                     Reporting Requirements1
en
CO
Incinerator Type
Recommended Report Organization
5.0 Sampling and Analysis Results
5.1 Methods Description

5.2 Waste Feed/Fuel Characteristics
• Physical characteristics





• Chemical characteristics







5.3 Stack Gas Concentration Data
• Gases
- CEMs




- Orsat


•POHCs
• Other




5.4 APCE Aqueous Streams



5.5 Ash and APCE Residues


1 Legend for reporting requirements:
Specific Information

Summary table
Diagram indicating sampling locations

Moisture
Ash
Volatile matter
HHV
Specific gravity
Viscosity
Chlorine
POHCs
Other Appendix VIII compounds
Metals
Fixed carbon
Elemental analysis
Heat capacity
Heat of Vaporization


CO
CO2
02
S02
NOX
TUHC
C02
02
Volatiles, semivolatiles, other analytes
Moisture
Chloride
Participate
Metals
PICs/other Appendix VII compounds
POHCs
ft hlnrirlo
IslllUriUD
TDS
pH
Metals
EP toxicity test results
POHCs
Metals

LFI

+ +
+ +

+ +.M
R.P.M
M
R,P,M
R
R",p4
R.P
R,P
0
0
M
M
M
M


R,P
R
P
0
O
+
+ +
R
R.P
R
R.P
R,P
O
O
-
.
-
.
-
-
•

RKI Q

+ +
+ +

+ +,M
R.P.M
-H-3.M
R.P.M
R
R4.P4
R.P
R,P
O
O
M
M
M
M


R.P
R
P
O
O
+
+• +
R
R.P
R
R.P
R,P
O
O
R
+ •
+
0
+ +5
R
05

Air Pollution Control Equipment
V PT IWS ME CY DS BH ESP

.
.......
-
.
.
.
.
.
.
.
.
.
.
.
.
.
..
.

.
.
.
-
.
.
-
.
.
.
.
-
.
.
R R R - - - - -
+ + '+ + +
+ +++ +
O O O 	
+ + O O
R R O O
0000

R = required by current regulation or EPA policy O = optional
P = required by this permitting guidan
ce F = standard form available
in Appendix B

             M  = needed for energy and mass balance model
             + + = standard practice/highly recommended
not applicable
recommended
           2 Standard forms available for all information in Process Operations Summary and Emissions Performance Summary
           3 Recommended for containerized solid waste
                                    4 Recommended for liquid waste fired in SCC
                                    5 Recommended for bottom ash

-------
 Table 5-2.   Trial Burn Reporting

  Typical Appendix Format	
Format and Requirements - Appended Information

                               Contents
Reporting Requirements1
  Detailed S&A Results
  • POHCs
  • Chloride


  • Paniculate
  • All analytical test results
  Raw Data Logs
  • Process data
  • CEM data
  • Stack sampling data
  Sample Traceability Records
  QA Results

  S&A Methods
  Chromatograms2
              Concentration in each sample
              Sampling durations
              Trip and field blank values
              Averages
              Concentration
              Impinger volumes
              Blank values
              Filter weights
              Laboratory reports/data

              Log sheets, strip charts
              Strip charts,  printouts
              Field data forms
              Sample collection, treatment, and analysis log
              Surrogate recoveries
              Blind audit samples
              Summary of standard method
              Description of any deviations
              "Nonstandard" methods
              Waste analysis
              Emissions analysis
         R
         R
         R
         R
         R
         R
         R
         R
         R


         R
         R
         R
        R
        R

        O
        R
        R

        R
        R
  1 Legend for reporting requirements:
   R  = required by regulations or can be required due to EPA policy
   O  = optional
  2 In some cases, one set of chromatograms may be requested by the permit writer. This may be a complete set of all chromatography-
   based analyses or only chromatograms from selected samples. Routine submission of chromatograms is not recommended due to their
   bulk.
 • A  measurement  of  average,  maximum,  and
   minimum  temperatures and  combustion  gas
   velocity

 • A continuous measurement of CO in  the  exhaust
   gas

 • Such other information as necessary to ensure that
   the  trial burn determines  compliance with  the
   performance standards and to  establish  the
   operating  conditions  required  to  meet  that
   performance standard

 • A certification that the trial burn has been carried
   out in accordance with the approved trial burn plan
   and  the results of all the determinations required
   [above]. This submission shall be made within  90
   days of completion  of the trial  burn, or later  if
   approved by  the permitting authority

 • All  data collected during  any trial  burn,  to  be
   submitted following the completion  of the trial burn

 • All submissions required [above] must be certified
   on  behalf of  the  applicant by the signature  of  a
   person  authorized to sign a permit application or a
   report

 The reporting  requirements  include  a mixture  of
 facility operation  results,  sampling and analysis
•results, and  performance results.  Certain quality
 assurance/quality control (QA/QC) results  may also
                          be required according to EPA policy. See reference 2
                          in Appendix  A  for  specific guidance materials  on
                          QA/QC requirements.

                          Some  information items listed in  Table 5-1 may not
                          be  essential  for  developing  incinerator  permit
                          conditions or conducting an energy and mass balance
                          but,  instead, may  be  required  under other  RCRA
                          regulations or regulations in support of the NPDES or
                          air  quality  permits.  These items are included  for
                          completeness and to indicate the  logical location in a
                          trial  burn  report where  the information  may  be
                          presented.  Some examples  include  chloride;  total
                          dissolved  solids  and  metals in  APCE   aqueous
                          streams; leachate extraction test results and metals in
                          solid residues;  and  gases  such as  SO2,  NOX, and
                          TUHCs in the stack  gas. The applicant may desire or
                          be requested to include these items in the  trial burn
                          report to present a more complete picture of the total
                          discharges of the facility in all media.

                          5.2.7 Suggested Report Format
                          The trial  burn report should be structured in a format
                          parallel to that  for the trial  burn plan  to facilitate the
                          review of the  report  and  simplify  the final  report
                          preparation. A  useful technique is to use  the same
                          section numbers and  identifiers  in  both  documents.
                          Assuming this   parallelism, the  remainder of this
                          section will discuss the report format only.
                                                    64

-------
          The trial burn report provides several distinct types of
          information for which a recommended general outline
          is  provided  below; a  detailed outline of specific
          information and requirements is  provided  in  Tables
          5-1  and  5-2 as  an  example  format.  The  tables
          provide an overview of all information that might be
          required or otherwise included in trial  burn  reports,
          although  no one  incinerator would  have  all  of  the
          components  covered in this  matrix. This ordering of
          information represents a logical sequence  of  results
          that can easily be followed by the permit reviewer. It
          is  for  illustrative  purposes; other  organizational
          techniques could also be acceptable. However, it is
          important  that all results needed for permitting be
          presented clearly,  and  unnecessary information
          should not be interspersed among them.

          The preliminary information  in the trial  burn report
          must include certification required  under 40 CFR
          270.62(b)(7),(9) signed by a corporate officer or other
          authorized agent  of the facility that the trial burn has
          been conducted according to the approved trial burn
          plan. It must also  include a preface identifying  the
          facility,  location, and  the  name of the company(ies)
          that performed the trial  burn  testing  and  sample
          analysis.

          Chapter 1  of the  report gives a summary of the test
          results as  well as of the facility information. It  should
          include  copies of Forms 1-4  of Appendix F for each
          test: The summary  data for each run can be given in
          the  appendix.  The purpose  of this  section is to
          summarize all pertinent  information required  for
          establishing  permit  conditions.  This  should be a
          "stand-alone"  section  that  provides  the  key
          performance  results,  operating  conditions, design,
          and facility information needed  for  permitting.  The
          section  consists of  several summary tables sufficient
          to explain the results. Appendix F gives examples of
          the summary forms  needed.

          The Introduction (Chapter  2)  should primarily  be text
          material "summarizing the  background of the  facility
          and the:type  of waste(s)  for which it was  designed
          and should include a summary of trial burn objectives
          and the planned test matrix. Any deviations from the
          planned test  matrix should be noted  and explained.
          Also to  be included here are brief descriptions of the
          types and sources of wastes and fuels to be normally
          burned  at  this facility as compared  to the  wastes
          burned  during the test as well as any  special  wastes
          or spiking  procedures used  for the trial. burn. The
          Introduction is also an appropriate location to describe
          any  unusual  (nonstandard) test  methods  used  and
          any special problems encountered in testing including
          sampling  and  analysis   problems  such   as
          breakthrough or loss of samples.

          The remaining three sections  should primarily contain
          detailed tables of results.  Chapter 3, Performance
          Results, summarizes data involving the  performance
    standards for  POHCs, chlorine,  particulate material,
    and  any applicable metal  limitations. This section,
    which is  a more detailed version of material supplied
    in Chapter 2, provides the values used in calculating
    the results.

    Chapter  4,  Process  Operating  Conditions,
    summarizes  all equipment operating conditions for the
    combustion chambers, APCE, and air/combustion gas
    moving equipment. A process diagram showing all the
    main  components of  equipment  and process
    monitoring locations should be included under Section
    4.1  of  the trial burn  report,  Process Overview. An
    example  of a process diagram is provided in  Figure
    5-1.  Note  that  Figure  5-1  is given  here  for
    simplicity; however,  a  permit  application  should
    include  a full  piping  and  instrumentation  diagram
    (P&ID). The  process monitors may be summarized in
    a table  referencing the locations indicated  on the
    diagram.  An  example is provided in Table 5-3.

    Section  5 in the  outline,  Sampling  and Analysis
    Results, is the final section of the main report body. It
    should  begin with a  subsection on  the  sampling
    method  used including a summary table of  sample
    types, sampling points, sampling  methods, frequency
    of sampling,  sample preparation steps, and analytical
    methods. A diagram of sampling locations should also
    be included.  Examples of the methods summary table
    and  sampling point diagram  are  given in Table 5-4
    and  Figure 5-2,  respectively. The  analytical results
    may logically be organized into four areas: waste feed
    and fuel, stack gas, APCE aqueous streams, and ash
    and other solid  residues.

    General reporting requirements for trial burn data that
    are  typically appended to  the  main  report are
    indicated  in  Table 5-2. The  appropriate regulatory
    agency will refine this list.

    The  appendices  to the  trial  burn report are  used
    primarily for  reporting raw data and supporting logs.
    "Detailed S&A Results"  can include data such as
    sample  volumes,  measured  concentrations  and
    weights,  calibration curves,  and response  factors.
    "Raw Data Logs" may include sampling data forms
    and  logs,  logs  of process  data, strip-charts,  and
    printouts from data loggers.  "Example Calculations"
    should show precisely the  processes by which final
    values were  obtained  for  the performance results.
    "QA  Results"  is  an  important  section  showing
    surrogate  recoveries,  blind audit  samples,  and
    calibration  data. "Sample  Traceability  Records" (or
    chain-of-custody logs)  show  the  movement  of  each
    sample  from collection to  final  analysis  and  any
    intermediate sample, splitting, compositing,  or
    treatment.  "S&A  Methods"   may include complete
    method write-ups, or it may  describe any deviations
    from  referenced  standard  methods  or  any
    "nonstandard"  methods  used.  Some  permitting
    agencies request that "Chromatograms" be included
k
65

-------
           Figure 5-1.   Example process diagram showing monitoring points.
en
O)
                                                                              ! 25 I
                                                                              v  A  Recirculated Scrubber Water
                                                                Secondary
                                                                Combustion
                                                                Chamber
               I QDQQQO!
           '—' DDQOQQ J
               l_BQBQBBj
               Drummed Solids
               Staging Area
To NPDES
System
                                      Ash Dumpster

-------
Table 5-3.   Example Summary Table of Process Monitors
Parameter
High-Btu liquid waste feed rate
Low-Btu liquid waste feed rate
Auxiliary fuel flow
Sludge waste feed rate
Drummed solid waste
charge weight
Atomization steam pressure
Rotary kiln temperature
SCC temperature
Quench inlet temperature
Quench discharge temperature
Adsorber temperature
IWS inlet temperature
Rotary kiln pressure (draft)
SCC pressure (draft)
Rotary kiln speed
Quench water flowrate
Caustic water flowrate
IWS water flowrate
Oxygen
Carbon Monoxide
Combustion gas flowrate
Combustion air flowrate
IWS electrical readings
Adsorber differential pressure
Scrubber water blowdown rate
Location of Monitor1
10A - Feed line to nozzle on SCC
10B - Feed line to nozzle on PCC
1 1 - Feed line to injector on SCC
1 2A - Fuel oil line to SCC
12B - Fuel oil line to kiln
1 3 - Feed line to injector on kiln
14 - Automatic weigh scale
at feed conveyor
15A - Waste burner in SCC
1 5B - Waste burner in kiln
16 - Kiln outlet
17 - Secondary chamber outlet
18 - Quench inlet
19 - Quench outlet duct
20 - Adsorber inlet
21A- Inlet duct to IWS No. 1
21 B - Inlet duct to IWS No. 2
22 - Rotary kiln chamber
23 - Secondary combustion chamber
24 - Kiln rollers
25 - Quench water line
26 - Caustic water line to adsorber
27A - IWS water line to unit No. 1
27B - IWS water line to unit No. 2
28 - IWS outlet duct
28 - IWS outlet duct
29 - Stack
30A - Air inlet duct to SCC
30B - Air inlet duct to kiln
31 A - Power lines to IWS electrodes for unit
No. 1
31 B - Power lines to IWS electrodes for unit
No. 2
32 - Adsorber inlet and outlet ducts
33 - Sewer line to NPDES system
Type of Monitor
Mass flowmeter
Mass flowmeter
Mass flowmeter
Mass flowmeter
Weigh scale
Pressure transducer
Type R thermocouple
Type R thermocouple
Type J thermocouple
Type J thermocouple
Type J thermocouple
Type J thermocouple
Pressure transducer
Pressure transducer
Tachometer
Orifice meter
Rotameter
Orifice meter
Zirconium oxide fuel cell
In situ NDIR
Resistance temperature
flow detector
Venturi meter
Voltmeter,
Mill-ammeter
Pressure transducer
Triangular weir
Operating
Range
0-100
0-100
0-100
0-100
0-2,000
0-100
2,650
2,650
150-600
150-600
150-600
150-600
-5 to 5
-5 to 5
0-1.0
0-200
0-50
0-50
0-25
0-500
0-100,000
0-60,000
0-20
0-200
0-20
0-12
Units
Recorded
in Process
Log
Ib/min
Ib/min
Ib/min
Ib/min
Ib
psig
°F
°F
°F
°F
°F
°F
in H2O
in H2O
rpm
gpm
gpm
gpm
percent
ppm
ACFM
ACFM
kV
mA
in H2O
in H2O
 1 Refer to Figure 4-1.
                                                       67

-------
Table 5-4. Example Summary Table of Sampling and Analysis Methods
Sample
Sample Frequency For Sampling Sample Analytical
Sample Location1 Each Run Method Size Parameters
High-Bill liquid
(organic waste)











Low-Btu liquid
(aqueous waste)










Auxiliary fuel
(fuel oil)

Sludge











Drummed solid
waste









Ininerator ash

Caustic solution

1 One grab
sample every
15 min
omposited into
one sample
for each run




1 One VOA vial
every 1 5
minutes5
2 One grab
sample every
15 min
composited
into one
sample for
each run



2 One VOA vial
every 15 min5
3 One per run


4 One grab
sample every
30 min
composited
into one
sample for
each run



4 One VOA vial5
every 30 min
5 One grab
sample every
other solid
charge,
composited at
end of test
Each sample
clearly
identified.


6 One grab
sample per run
7 One grab
sample per run
Tap
(S004)








Tap
(S004)

Tap
(S004)








Tap
(S004)
Tap
(S004)

Tap
(S004)








Tap
(S004)
Scoop
(S007)









Scoop
(S007)
Tap
(S004)
~100mL
per grab








40 ml
per vial

-100 mL
perg








40 mL
per vial
250 mL


-100 mL
per grab








40 mL
per vial
~250 g
per grab









500 g

500 g

SV POHC3
Heating value
Ash
Viscosity
Chlorine



Elemental
analysis
V POHC6


SV POHC
Heating value
Ash
Viscosity
Chlorine



Elemental
analysis
VPOHC

Heating value
Ash
Density
SV POHC
Heating value
Ash
Viscosity
Chlorine



Elemental
analysis
VPOHC

VPOHC

SV POHC
Chlorine



Elemental
analysis
Heating value
Ash
SV POHC

Archive

Preparation
Method2
Solvent dilution
NA
NA
NA
NA





Dispersion/purge
and trap

Solvent extraction
NA
NA
NA
NA





Dispersion/
purge and trap
NA
NA
NA
Solvent extraction
NA
NA
NA
NA





Dispersion/
purge and trap
Dispersion/
purge and trap
Soxhlet extraction
NA





NA
NA
Solvent extraction

NA

Analytical Method2
HRGC/MS4
Calorimeter (D240-73)
Ignition (D482-80)
Viscometer (D-88-81)
Organic halide
(D808-81 and
D4327-84) or
(E442-81)


HRGC/MS


HRGC/MS4
Calorimeter (D240-73)
Ignition (D482-80)
Viscometer (D-88-81)
Organic halide
(D808-81 and
D4327-84) or
(E442-81)7


HRGC/MS

Calorimeter
Ignition (D482-80)
Gravimetric
HRGC/MS
Calorimeter (D240-73)
Ignition (D482-80)
Viscometer (D-88-81)
Organic halide
(D808-81 and
D4327-84) or
(E442-81)7

',.
HRGC/MS

HRGC/MS

HRGC/MS
Organic halide
(D808-81 and
D4327-84) or
(E442-81)7


Calorimeter (D201 5-77)
Ignition (D482-80)
HRGC/MS

NA

68

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Table 5-4.    Example Summary Table of Sampling and Analysis Methods (continued)
Sample
Scrubber water
blow/down








Stack gas



•...". -

Sample
Sample Frequency For
Location1 Each Run
8 One grab
sample every
30 min
composited ..
into one
sample for
each run
8 One VOA vial
every 30 min5

9 2-hr
composite per
run



Sampling
Method
Dipper (S002)






VOA vial filled
from grab
sample
MM59





Sample
Size
4L






40 mL
per
VOA
60-100
cuft10




Analytical
Parameters
SV POHC
Specific
conductivity




VPOHC


Particulate
HCI

Moisture
Temperature
Velocity
Preparation
Method2
Solvent extraction
NA





Purge and trap


Desiccation
NA

NA
NA
NA
Analytical Method2
GC/MS8
Conductivity meter





GC/MS


Gravimetric (EPA RMS)
IC12 (D4327-84)

Gravimetric
Thermocouple
Pitot tube
                            2-hr               MM5      60-100   SV POHC
                            composite per                   cu ft10   Moisture
                            run                                    Temperature
                                                                   Velocity

                            3-4 trap pairs       VOST       20 L    VPOHC
                            per run            (S012)12     max. per
                                                          trap pair
                                                             Solvent extraction   HRGC/MS
                                                             NA               Gravimetric
                                                             NA               Thermocouple
                                                             NA               Pitot tube

                                                             Purge and trap     GC/MS
 City water
                     9      One composite     EPA Ref.
                            sample per run     Method 3
                                       -20 L  Oxygen, CO     NA
                            Continuous
10     Once pretest
                                                NA
 Tap
(S004)
                                       NA    CO
                                   NA
NA    Ash, chloride   NA
                                                    Orsar
NDIR continuous monitor,
specific extracting or in
situ
Gravimetric, 1C
 NOTE: Sampling method numbers (e.g., S004) refer to methods published in Sampling and Analysis Methods for Hazardous Waste
        Combustion, December, 1983; analytical methods beginning with prefixes D and E refer to ASTM methods.
 NA = not applicable.
 1 Refers to Figure 4-2; give P&ID reference number.
 2 Sample preparation and analytical methods reference the A. D. Little, EPA 600 and SW-846 methods.
 3 Semivolatile principal organic hazardous constituent.
 4 HRGC/MS = high resolution gas chromatography/mass spectroscopy.                                                 .
 5 VOA = volatile organic analysis. All VOA vials from each run are composited just prior to analysis,
 6 Volatile principle organip hazardous constituent.
 7E442-81 is used for samples  with  high (> 0.1%) concentrations, and  D808-81  and  D4327-84  are  used for samples  with  low
  concentrations, .-••-••v
 8 GC/MS = gas chromatography/mass spectroscopy.
 9 MM5 = Modified Method 5 (EPA Reference Method 5,  Modified), SW 846, Method 0010.
 10 Exact volume of gas sampled is dependent on isokinetic sampling rate.
 11  Ion chromatography.
 12 VOST =  volatile organic sampling train.
                                                           69

-------
         Figure 5-2.   Example of process diagram showing sampling locations.
-si
o
                                                                                   Recirculated Scrubber Water
                                                                                                     »
                                                                Secondary
                                                                Combustion
                                                                Chamber
             ,'  DQOQOQ !
             '  QBQQQB ;
             Drummed Solids
             Staging Area
ToNPDES
System
                                      Ash Dumpster
                                                                              (    j  Sampling Point

-------
for organic analysis of both the waste feed and stack
emissions;  however, this  information  can  be
voluminous and  should not  be included with  every
copy of the report.

5.2.2  Guidance  for Reporting  Process  and
Continuous  Emissions Monitor (CEM) Data
Ideally,  measurement of incinerator  performance
would  be  done  on a  real-time  basis;  however, a
certain  amount of  time averaging must be used to
evaluate and report trial burn data. Most of the  trial
burn  data fall  into  two categories:  data  that must
represent an average over the test period or portion
of  the  test period  and  data that  is  recorded
continuously or  semicontinuously.  Data that by
necessity  are an  average  include  most  of  the
analytical results, e.g., waste characterization results
for a composited sample of waste feed as  well as
Modified Method  5  (MM5)  or  Volatile  Organic
Sampling Train (VOST) results for a sampling period
of minutes to hours.  Data taken continuously (or as
continuously  as practical) include  both process and
CEM data.  This section discusses primarily  the
method  by which  continuously monitored data  are
processed and reported.

Process and  CEM data needed for the trial burn  are
shown in Table 5-5. Sixteen  parameters of this type
are required for establishing permit conditions that fall
into groups  A,   B,  and  C.  Additional  parameters
needed to support  the permitting process are also
shown although others, not specified  here, may be
required  at  the  discretion  of the  permit  writer.
Parameters  that are related  primarily to waste
analysis  (e.g., ash and halides input) are  not included
here. As discussed in Chapter 2, group  A and B
parameters  are  those which  require  continuous
monitoring of process instrumentation  and are tied to
automatic waste feed cutoff.  In addition, their status
must be continuously monitored as described below.
Specific  RCRA requirements  apply only to  the group
A   parameters.  Permitted  operation  requires
continuous monitoring of combustion temperature,
CO, waste feed rate, and a combustion  gas velocity
indicator (40 CFR  264.347(a)(1,2))  with automatic
waste feed cutoff tied in if permit limits are exceeded
(40 CFR 264.345(b,e)). The level of .CO  in the  stack
gas is the only parameter which by RCRA regulations
specifically state  must be  continuously monitored
during  the trial  burn  (40  CFR  270.62(b)(6)(ix)).
However, the incinerator  should already have  had
continuous monitors installed  for  temperature, feed
rate, and gas velocity to obtain approval for the trial
burn  because  measurements  of  continuous
operations should be taken with the same instruments
used during the  trial  burn.  Draft or  pressure
measurement, presumably on  a continuous basis, is
also required  by  RCRA to  ensure  that fugitive
emissions are not released (40  CFR 264.345(d)). The
RCRA  regulations require reporting of the trial burn
average, minimum, and maximum only for combustion
temperature  and  gas  velocity  (40   CFR
270.62(b)(6)(viii)). A measurement of QZ level in  the
stack  gas  is  also  required  by  RCRA  (40  CFR
270.62(b)(6)(ii)). Continuous measurement is required
per  this  guidance  and  other  guidance  material
primarily to  correct  CO levels to a standard value of
02-  Based  on this guidance,  continuous monitoring
and  waste feed cutoff interlocks for important APCE
parameters should also be required.
Table 5-5.   Process and CEM Data Requirements

 Permitting
   Level	Parameters	

    A     Combustion temperature for each chamber
    A     CO level in stack gas
    A     Indicator of combustion gas velocity
    A     Pressure in PCC
    A     Waste feed rate of each stream to each combustion
          chamber

    A     Differential pressure across venturi scrubber
    A     Differential pressure across FF
    A     Absorber water flowrate and pH
    B     Voltages and amperages for ESP or IWS
    B     POHC and halides in waste
    B     Size of containerized waste to PCC
    B     Particle scrubber blowdown rate
    C     Heat input rate for each combustion chamber
    C     Burner turndown for LI chamber
    C     Atomization pressure for LI chamber
    C     APCE inlet gas temperature
          Oxygen level in stack gas
          Quench water flowrate
          Quench water temperature
          Auxiliary fuel feed rate
          PCC/SCC air flowrate
Group B and  C parameters require  maintenance of
operating records. Parameters in group B require the
use of trial burn data to establish  permit conditions.
Group C  parameters,  on the  other  hand,  are set
independently  of  trial burn  conditions according to
manufacturer specifications.  Nevertheless,  group C
parameters must still be  measured  during  the trial
burn to demonstrate compliance with the permit  limits
that are based upon those specifications.

Some  of  the  process  and  CEM  data shown are
needed  for the energy and mass balance model, if it
is to be used. Waste and auxiliary fuel feed rates are
required for the model. Combustion gas velocity may
be used as an alternative to design ID fan capacity;
and measured APCE inlet temperature, quench water
flowrate, and quench water temperature may be  used
instead of the design maximums. Finally, primary and
secondary combustion air flow  rates  and   ash
generation  rates,  if  available, need to  be  measured
                                                  71

-------
during the trial  burn and  reported  for use in the
energy and mass balance.

Operating records  must be  used to  report trial burn
values  for  group  C  parameters  and  any  other
parameters needed for the energy and mass balance.
The size of containerized waste to the PCC may be
described in the text in Section 4.2 of the trial burn
report.  The maximum volume and  mass  used  for
each containerized waste must be reported along with
the  interval  between  Charges. The  paniculate
scrubber blowdown  rate  for each test run is  based
upon readings taken at regular intervals (1 hr or less).

The heat input rate for each chamber is reported  for
each test run. It is based on  the heating value and
average feed rate of each composited waste and fuel
stream. Burner turndown  should be reported for each
burner using design  maxima  and the average feed
rate of the waste. Atomization  fluid pressure for each
burner on the  liquid injection chamber should also be
reported.  An average of readings taken  at regular
intervals (1 hr or less) is usually sufficient.

The APCE inlet gas temperatures  do not  normally
vary significantly. To report an average of  readings
taken at regular intervals  (minimum  of  15 min) is
sufficient. Averages of  readings  for  the  trial  burn
period need to be reported for quench water flowrate,
pH, and temperature. Again, readings taken  at regular
intervals  of  at  least 15  min are  recommended.
Primary and secondary combustion  air flow rates, if
available,  should 'be reported with  at least 15-min
readings used for the average.

Power readings on  the blowers along  with calibration
curves for conversion to flowrates should be reported
if air flowrates are  not available. The  ash generation
rate for each run   involving solid waste should  be
reported. This rate  is normally  based upon the weight
of all the ash collected during  the test period.  As  an
internal  consistency  check,  it  may be worthwhile to
compare this value to the amount of  ash fed  to the
incinerator as  determined by the waste analysis and
flowrate.

Example reporting  forms  for process  and CEM data
are located in Appendix F. The forms are divided into
categories of combustion equipment,  stack  gas data,
and APCE data.

Reporting Continuously Monitored  Parameters
All the group A parameters (as defined in Chapter 2)
must be monitored  continuously during the  trial burn
as well  as during subsequent operations.  Using the
recorded  data for  the  trial  burn test  period,  an
average, maximum,  and  minimum must be  reported
for 'each  parameter.  For  each  run,  reporting
approaches will vary according to  the instrumentation
utilized.  Some  facilities may  use  strip-chart
recorders  for recording the data,  and some will use
computerized  data. loggers., Because data  loggers
often use  strip-chart  recorders  as  a backup,  both
types of information  may  be available.  Continuous
recording, which is  available only through strip-chart
recorders,  is not necessarily  required, although it is
recommended that data be read in some manner at
least every  15 ,sec  and that a value be recorded at
least every minute.  Either strip-charts or data logger
printouts for  the  trial1 burn period  are normally
included in  an  appendix to the trial burn report.

Averages, minimums,  and maximums for each of the
A and  B parameters:,may be calculated  using  either
strip-charts or data  logger printouts.  In  some cases,
both types of hard  data .may be used  for a single
parameter (e.g.,  maximum  and  minimum from strip-
chart recording  and  time-weighted; average from
data logger printout).  Each  basic approach  is
described rbelow.    ,.  . .... .:   .            -:

Use of data  loggers: Data  Joggers are  normally
equipped to  provide,  a  time-weighted  average  of
readings taken within the interval between printing or
recording.  In general,  during   hazardous  waste
incineration, readings  should be taken every minute.
These  frequent readings  are  needed,as  part of the
continuous  record unless strip-charts  are  also
available. In addition, for the trial burn, it is useful to
program the data logger to print out time-weighted
averages  for  a longer  period,   typically  15  min.
Following  the trial  burn,  the   15-min  averages
corresponding  to the  sampling period may then be
used to determine  the average, for each run; this is
done by simply determining the arithmetic mean of all
of the appropriate readings.             ,

Some data loggers  can be programmed to print out
the minimum and maximum readings taken within the
period  between printing. If this approach  is used to
determine the  minimum and maximum for each trial
burn run, the printouts must be  examined for all the
sampling period. The lowest interval minimum and the
highest interval maximum  must  then be reported. If
the data  logger does  .not record  interval minimums
and  maximums,  these must  be  read off the  strip-
chart, as explained below.   .          .

Use of Strip-charts:  The  use  of  strip-charts  for
determining  minimums and  maximums is relatively
straightforward. . The main  problem  is .one  of
calibration.  The strip-chart must be legible, and units
of instrument  readings  and time  must. be clearly
visible. The recording  should be checked against the
instrument gauge or read out at several  values just
before  or  during the  trial  burn.  These  instrument
readings should be  marked on the strip-chart paper.
At the  start and  end  of the trial burn run,  the  time
should  be marked  on the x-axis of the. paper as a
cross-check. The date,' operator .initials,., notes about
run numbers,  and  other .comments  should also be
recorded. Interruptions in sampling should be marked
                                                 72

-------
 on the strip-charts so that  the  nonsampling interval
 will not be included in determinations of the minimum,
 maximum, and average.

 Special data-handling problems  exist if  the range of
 the  strip-chart  is  exceeded  for  the maximum  or
 minimum. Each exceeded time off scale and minimum
 or maximum value  should be recorded.  For example,
 if the kiln  temperature  spiked  downward offscale
 every  time  a drum of chlorinated still  bottoms  was
 fired,  the reported minimum  temperature  might be
 "<700°C  for  16 min  (24  exceeded ranges)." Of
 course, it is best to ensure  that  the strip-chart has a
 range  wide enough to avoid such offscale readings
 for determining averages. While they may be used in
 some  cases, offscale readings may limit the flexibility
 in permit limits for the facility.  For  example, in  the
 case above, to report 700 °C temperature for 16 min
 when the actual temperature was lower will result in a
 higher permit limit  for temperature than if  all values
 were recorded. Upward  temperature  spikes  that go
 offscale, on the other hand,  would  not be allowed for
 establishing a permit limit.

 Other  approaches to  using  strip-chart   data  are
 available. Devices such as a planimeter can integrate
 under  the trace. Computerized methods  in which  the
 recorder trace is  optically or mechanically  entered
 into  a data base may also  be applicable.  The data
 base  can  then  be  used to calculate the time-
 weighted  average,  minimum, and  maximum.  The
 major  concern  with all these approaches is that the
 strip-chart must be appropriately calibrated and the
 device must account for instrument calibration factors
 and  nonlinear responses. The approach to be used
 by the applicant should be specified  in the trial burn
 plan and approved by the permit  reviewer prior to the
 trial burn.
Special Problems
Most  process  instruments   produce  nearly
instantaneous electrical signals that may be read off a
gauge  or  processed in  a data logging system. The
CEMs, however, are generally not as responsive to
changing conditions. Delays are caused  by  the gas
stream physically moving through a sampling line, and
instrumental delays are caused by a sensor that must
adapt to changing gas composition. For a given gas,
one type of instrument may be more responsive than
another. For example, paramagnetic oxygen monitors
respond more rapidly than do electrochemical types.

Combined  delays for  sample  lines,  conditioning
systems,' and  instruments  may  range  from several
seconds to several  minutes. The CEM system may
be  responsive in "tracking"  a small  change  in
concentration but not a large, sudden peak or dip.
Delays such as these are  important  to consider for
permit  conditions  involving time-delayed  waste feed
 cutoff. This type of problem should be worked out as
 early as possible in the trial burn planning stage.

 Another general  data quality problem  common to
 most trial  burn tests involves the correlation  of the
 performance results  with the  operating conditions.
 Different measurements  span different time periods.
 The trial burn run can easily span 6 to 8 hr or longer
 as analytical detection  limits  often  dictate  actual
 sampling times. An  additional  problem  may  occur
 during the test when unavoidable variations  in waste
 properties  and other factors cause the unit to deviate
 from  the planned  conditions. Variations in  process
 conditions  outside  the  planned  ranges can  make
 correlating sampling results difficult. An  example trial
 burn  run timeline is shown in Figure  5-3 to  illustrate
 these correlational problems.

 Figure  5-3 shows  how  the  various  sampling  and
 monitoring activities are coordinated during a typical
 trial burn run. Six 40-min VOST samples were taken
 during the  run ("Slow VOST" at  0.5 L/min) for a total
 of 4 hours  of volatile sampling. Two  MM5 trains were
 used: one  for particulate sampling and the other for
 semivolatile POHCs. Each train sampled for CI". One
 train  was started several minutes before the  other.
 The total sampling time for  MM5 was 6 hr with a port
 change midway to traverse the stack  again at  a 90°
 angle to the first traverse for isokinetic  sampling.

 Grab  sampling was  used for waste feed and scrubber
 liquids with compositing during  or following the test.
 The waste feed  was sampled  at 12-min  intervals
 and  the scrubber  liquid and bottom ash  at 1-hr
 intervals.  Grab sampling of  liquids  was  briefly
 discontinued during  the MM5 port changes for the
 best achievable correlation  of POHC inlet and outlet
 measurement, but  sampling of  waste continued as.
 solids retention  time is normally greater than 30 min.
 The fourth  VOST sample  was also delayed until MM5
 sampling continued. Logging of process and CEM
 data was continued  during this interval.

 Logging  of process and CEM data must occur over
 the entire period of  any sampling activity. This period
 of any concurrent  sampling activity and  logging
 becomes the formal trial  burn period for that run. In
 the case illustrated  in Figure 5-1, the trial burn run
 period is from 10:00 to 15:36 and from  17:06 to 18:12
for a total test time of 6.7  hr. The actual time required
 was 8.2 hr due  to a 1.5-hr process upset  when
 sampling and logging were discontinued because a
 process parameter deviated outside the  planned  trial
 burn  range. It  should be noted that sampling  and
 logging  of  data may be  discontinued only  when a
 major process  upset occurs that prevents  proper
waste incineration. In such a case, the run can only
 be considered a successful run  if permit conditions
can be written such that the conditions triggering the
upset  will   not  occur in  subsequent  operation.
Otherwise,  sampling must  be continued  during
 "upset" conditions,  and the results of that run must
                                                 73

-------
 Figure 5-3.  Example of trial bum test timeline.


                   Sample 1  Sample 2  Sample 3

 (Volatile POHCs)
 MM5 Tfain No. 1
 (Cl, Paniculate)
MM5 Train No. 2
 (Cl, SV POHCs)
 Grab Sampling:
 Waste (
 APCE Liquids •
 -Bottom Ash *
 Logging of Process
 and CEM Data
Process Parameter
 (e.g., Temperature)
                                 Sample 4   Sample 5
                                       Sample 6
                           _, Port j_
                           'Change
                           -»Port K-
                            Change
*\l/V*ry*WS/<\*^/^^^                           I  .    jAA^^/^^^^AAVt^v/vv
                                                                 i Proccess Upset
                         I
                                                   I
                                                            I
              1000     1100
                1200
1300
1400     1500

  Military Time
1600
1700
1800
1900,
be  reported. The  CEMs and logging of data  must
continue whenever hazardous waste is being fed to
the incinerator.

It is necessary to  report all minimum and maximum
parameter values measured during a test to provide
the data heeded to set these limits. For example, if
the temperature drops to a minimum during the trial
burn and remains  constant for a period, that period
should  be  reported along with  the  minimum
temperature. If  there is more than one period of the
same minimum temperature,  the  total time  at  this
minimum value  would  be reported.
Processing and Reporting CO Data
The stack gas CO concentration is considered to be
a  real-time indicator  of  incinerator  performance.
Although CO levels cannot be directly related to ORE
at high levels of ORE, on a site-specific basis,  CO is
a useful indicator of overall performance. Because of
the interdependency of CO  levels and  incinerator
monitoring, specific guidelines for CO are necessary.
Separate guidance manuals on CO monitoring and on
CO limits  for  hazardous  waste  incinerators  are
currently under development by EPA.
                                     5.3  Operational  Recordkeeping  and
                                     Reporting
                                     Recordkeeping requirements for permitted operation,
                                     although not part  of  trial  burn reporting, are  briefly
                                     mentioned  here because  of the close association
                                     between reporting trial  burn data and  establishing
                                     permit limits.
                                     Operational  logs  constitute the major source  of
                                     records for the facility. The exact format of the log is
                                     left to  the  facility because  it  includes  important
                                     information  for the operator  (e.g.,  damper  settings
                                     and  tank  level readings)  that is not necessary for
                                     establishing  permit  conditions. .The  logs  must,
                                     however, include all appropriate information needed to
                                     demonstrate  compliance with  permit limits.  Units of
                                     measurement may be the  same as  the instruments
                                     record as long as  they may be  readily converted to
                                     units appropriate to the permit limits. Each,instrument
                                     should be  identified  with  a  code  number,
                                     manufacturer's name and  model number,  or other
                                     unique  identifier. Detailed  information, the", operating
                                     principle, and calibration method for each instrument
                                     type are normally  required  in the permit application,
                                     and  the  log  should reflect these information
                                     requirements.
                                                 74

-------
         In addition to  operating logs  for process data,  logs
         that relate to waste characteristics are also  essential
         for compliance with permit limits. Reporting forms for
         demonstrating compliance with the maximum permit
         limits  on halides and inorganic ash are provided in
         Appendix F.  It is  also  recommended  that   the
         permitting authority require that the facility record in
         the operating log the dates, times, and reasons for
         any permit violations or  any automatic waste  feed
         shutoff along with corrective actions taken, as well as
         any instances where the automatic  waste shutoff
         system was not activated  when parameters reached
         shutoff levels, the  reasons, and  corrective actions
         taken. The proposed amendments to the incinerator
         regulations  include  a   requirement  that such
         information be compiled into a report to be submitted
         to the permitting authority on a quarterly basis.  The
         permit writer  may wish  to  include  this  type of
         reporting requirement in the permit.


         5.4 Available Computer Program Support
         Two computer data bases are available  that can be
         used by  permit applicants to increase knowledge of
         incineration systems:  1)  Hazardous Waste Control
         Technology  Data Base and 2)  Energy and Mass
         Balance Model Requirements.

         Hazardous Waste  Control Technology Data Base
         The HWCTDB,  which is jointly funded by the EPA's
         HWERL and the DOE through the Oak Ridge National
         Laboratory  (ORNL),  is a  source  of  detailed
         information on  thermal treatment technologies  that
         may  be  useful  in the permitting process.  The
         HWCTDB is a compilation of data  from regulations,
         guidance manuals,  permit applications, and trial burn
         reports submitted  to the  EPA. The  information is
         retrievable thrpugh  a menu-driven   system,  and
         customized  reports  of summary  information  and
         itemized data listings can be obtained online.

         Parameters in the data base have been grouped  into
         five areas for ease of retrieval and selection:

         1. General facility information
         2. Design information
         3. Waste  characteristics
         4. Operating conditions
         5. Trial burn results
            ."    '; ~-i ':? -'•;.; :"        ,

         Within these  parameters,  HWCTDB provides
         information on the following:

         • Existing  thermal treatment facilities and their
           capabilities
         • Trial burn and design data

         • Heating valiies

         • Waste  components and concentrations
    • ORE

    • Permit status  for existing, new,  and  research,
      development, and demonstration facilities

    The data base is  currently operated by ORNL, which
    has produced search forms that permit writers  may
    use to access data on  waste feed  characteristics,
    capacity,  incinerator  design,  and performance.  A
    sample form for collecting trial burn data is included
    in Appendix F.

    Energy and Mass Balance Calculation
    To facilitate performance of energy and mass balance
    calculations for  hazardous  waste  incinerators,  a
    computer model has been developed under an  EPA
    contract by EERC. The  model is currently in  draft
    form and is being reviewed by EPA. The model can
    assist  the permit  writer in evaluating  incinerator trial
    burn and design data to develop consistent operating
    conditions.  The use of this  model  is  discussed  in
    Appendices B and E of this handbook. A sample  form
    for the engineering analysis data is also provided  in
    Appendix E.

    5.5 Recommended Forms for  Presenting
    Data  Summaries
    Appendix F  contains 12 forms which can be useful  in
    presenting the information needed to  evaluate a trial
    burn. While  it is recognized that no one set of forms
    can include all  variations  of incinerator system
    designs, these should, if possible,  be  used as  a
    guide.  Use  of the forms  will help the  permit writer
    identify key  pieces of information quickly and facilitate
    the evaluation process. The forms in Appendix  F  fit
    into three categories:

    1. Summary of the facility  and target operating ranges

    2. Summary of average operating conditions during
      each test condition of  the trial  burn. Note that  a
      minimum  of three  runs at the same operating
      conditions constitute a test

    3. Summary of the key  parameters monitored  and
      measured during each run

    Table  5-6  lists the  12 forms in  Appendix F  and
    summarizes how they are used. The first two tables
    simply summarize the general facility information and
    the general  design and operating  information.  Some
    operating  information in Form  2 can  be given  as  a
    range.  The  purpose of Form  2 is  to summarize the
    facility's major attributes and to serve  as  a  guide  to
    the permit writer.
L
75

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 Table 5-6.    Recommended Usage of Sample Forms in Trial Burn Report

   Form                                                    No. of
   No.	Title	Copies
                           Purpose
    1    Summary of Facility Information                         1


    2    Summary of Design Information                         1


    3    Description of Waste Streams                           1


    4    Summary of Test Conditions (Waste Feed)             1 per test


    5    Summary of Operating Parameter Values               1 per test

                                                         1 per run



    6    Summary of System Performance                     1 per test

                                                         1 per run



    7    Method 5 and Participate Results                     1 per run



   8a    Input Rates                                       1 per run



   8b    Chloride Emissions                                 1 per run
   9a    POHC Emissions (may be used for volatiles and         1 per run
         semfvolatiles or use Form 9c for semivolatiles
         separately)
   9b    POHC Input Rates                                 1 per run
   9c    Semivolatile POHC Emissions (may be used in lieu of     1 per run
         Form 9a for semivolatile emission results)


   10    Monitoring Data for Halides and Inorganic Ash and       1 per run
         Operations


   11    List of Samples                                    1 per test

   12    Emergency Shutdown and Permit Compliance Record        1
     To indicate the range of values that would be encountered
     during operation or to describe the facility
     To indicate the range of values that would be encountered
     during operation or to describe the facility
     To indicate the range of values that would be encountered
     during operation or to describe the facility
     To summarize the results of each test, i.e., average of the
     runs for that test condition1
     To summarize the results of each test, i.e., average of the
     runs for that test condition
     To summarize the results of each run. The average of these
     data for each test constitute input to summary of the results
     of each test.
     To summarize the results of each test, i.e., average of the
     runs for that test condition
     To summarize the results of each run. The average of these
     data for each test constitute input to summary of the results
     of each test.
     To summarize the results of each run. The average of these
     data for each test constitute input to summary of the results
     of each test.
     To summarize the results of each run. The average of these
     data for each test constitute input to summary of the results
     of each test.
     To summarize the results of each run. The average of these
     data for each test constitute input to summary of the results
     of each test.
     To summarize the results of each run. The average of these
     data for each test constitute input to summary of the results
     of each test.
     To summarize the results of each run. The average of these
     data for each test constitute input to summary of the results
     of each test
     To summarize the results of each run. The average of these
     data for each test constitute input to summary of the results
     of each test
     To summarize the results of each run. The average of these
     data for each test constitute input to summary of the results
     of each test
     As a QA/QC check on the samples taken during the test
     Operation only
  Note: Submit pages that have been copied on one side only to facilitate evaluation and review.
  11f waste composition changes for each run, then Form 3 should be included to identify the actual composition of the wastes burned during
    each run.
 Form 3  describes the waste streams that the  facility
 will burn both during  normal operation and during the
 trial  burn.  Different  wastes  may  be  burned  during
 these  two  operations, for example,  to  fortify one or
 more waste streams with a specific POHC or to push
 the system to an extreme for the trial burn. Form 3 is
 used,  therefore,  to summarize  the  data  for  three
 different purposes.  First,  they   can  be  used  to
 summarize   the   ranges  of  waste  types  and
•composition  that the facility  will burn during normal
 operation. This  summary, along with  Forms 1  and 2,
 constitutes the  overall   facility  summary.   Second,
 Form 3  can be  used  to  summarize the waste burned
at each test condition. For this  purpose, the  forms
present the summary of the  runs constituting  each
complete test. Finally, Form 3 can be used to present
the  information  on the wastes burned  during  each
run. As can be seen, the averages of the information
entered at this  point form  the input for  the second
purpose.  This approach presents the information in a
concise format  which the  permit writer  can use  to
determine  quickly  how  summary  results  were
obtained.

Forms 4,  5, and 6 are used in a similar manner as
Form 3. They can be used to present  the operating
                                                          76

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conditions of the incinerator during each run.  It can    They would normally be presented in the appendix to
also  be  used to summarize  the mean operating    introduce the  raw data log for each run. Form 10 is
conditions during  each test. Once again, the same    only used if an emergency shutdown occurred during
form is used to present data at two summary levels.      the  trial  burn.  It  is  intended to  document  the
                                                    occurrence and the  conditions which caused it.
Forms  5 through 9 are intended to summarize some
of the raw data on the performance of the incinerator.
                                                77

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                                            CHAPTER 6

                            Inspection and Maintenance Guidelines
A  regular I&M  program is critical to the successful
operation of the  incinerator facility.  The  primary
objective of the I&M program is  to ensure that major
equipment  is operated  safely, reliably,  and  according
to manufacturer operating specifications. Additionally,
the  I&M program addresses  the  calibration  and
maintenance  of  monitoring equipment  used to
establish the accuracy  and reliability of process  data
that  must  demonstrate compliance with regulatory
limits imposed in the operating permit.

Any  hazardous waste incineration facility is required
to adhere to an I&M program (40 CFR 264.347). The
permit  applicant  must detail this program  in the
application. The  information should  address  the
specific I&M activities for major  system  components
and monitoring instrumentation including the proposed
I&M  frequency. The  permit writer  relies on  this
information  because I&M requirements  are specific to
the type of  equipment, its intended operation, and the
manufacturer.  On the basis  of  this information  and
other recommended guidelines discussed below, the
permit  writer specifies  the  type of  I&M program
applicable to the facility under review.

Table  6-1  summarizes  a  recommended  permit
approach to  the  I&M program.  Details  of the  I&M
program and general  guidelines  are discussed in the
following  sections.

6.1 General Facility Equipment
Incineration  equipment  and  APCE  should be
inspected daily or weekly to verify the operational
status.  This  frequency implies an outside  visual
inspection of the equipment rather than a systematic
component inspection. A  detailed  inspection of
incinerator  refractory,  scrubber  nozzles,  or  fabric
collector bags, which would  require a system
shutdown, is recommended on a much less frequent
schedule, as specified by the  particular equipment
manufacturer.  Occasionally, a piece  of equipment
may  indicate a potential  problem.  In  this  event,  a
detailed inspection of those equipment components is
necessary to ward off  potential  noncompliance  with
RCRA performance specifications. Such problems are
generally manifest  through a variety of performance
indicators.
 Tables  6-2  and  6-3  list  indicators  of  poor
 performance, the  equipment problems  generally
 associated with these indicators, and  recommended
 maintenance and  troubleshooting" programs.  If the
 facility cannot correct  the  problems by  operational
 adjustment (within  the limits of the operating permit),
 the equipment generally requires detailed inspection
 and  possible repair. Appropriate troubleshooting and
 repairs should then  be implemented  to  prevent
 possible  safety risks or noncompliance  with  permit
 requirements. The inspection,  maintenance,  and
 troubleshooting practices recommended in Tables 6-
 2 and  6-3 require,  in most cases, that the incinerator
 facility be shut down.

 Operational  and performance  monitoring
 instrumentation such  as liquid  (pumpable)  waste
 flowmeters,  water  flowmeters,  pH meters, and  CO,
 temperature and 02 continuous recorders should also
 be subjected to a  routine inspection and maintenance
 program. A visual  inspection of this equipment should
 be carried  out  on  a daily  basis if  possible.  In the
 longer  time frame,  thermocouples should be
 inspected to determine whether the ceramic shields
 show signs  of cracking or deterioration. Monitors for
 O2 and CO should be inspected at  clearly specified
 intervals  for proper gas flowrate, vacuum  pressures,
 and  potentiometer  settings. The gas  conditioning
 systems that support this instrumentation should  also
 be inspected to determine possible air  inleakage and
 moisture  dropout efficiency. Any  supporting
 electronics  hardware should also be inspected.  The
 continuous  monitoring response  of  this  equipment
 also  provides a continuous readout of  instrument
 functionality.

The maintenance program for this equipment includes
routine service and calibration  activities.  Service
requirements  are normally  specified  by  the
manufacturer, as  they  are  specific  to  the type of
instrumentation used.  Response  and  calibration
checks should be  performed regularly. For gaseous
analyzers for 02 and CO (and others  if required by
regulations other  than  RCRA),  calibration  and
response checks should be  performed daily because
these instruments  are subject  to drift and  reduced
sensitivity.
                                                 79

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Table 6-1.    Recommended Inspection and Maintenance Frequency
                                                                                Inspection and Maintenance Frequency
Equipment/Parameter
Incinerator equipment
Waste feed/fuel systems
PCC and SCC outlet gas
temperature
Oz and CO monitors
Gas flow monitors
• Direct gas velocity
• Indirect fan amps
Other incinerator monitoring
equipment (flame scanners, air
blowers, etc.)
APCE
APCE support systems
APCE performance instrumentation
Inspection and Maintenenace
Criteria
Proper Operation
Proper Operation and Accuracy
Proper Operation and Accuracy
Proper Operation and Accuracy
Proper Operation and Accuracy
Accuracy
Proper Operation
Proper Operation
Proper Operation
Proper Operation and Accuracy
Operation and
Calibration
-
2
Monthly
Daily
Monthly
6 Months
'"


Weekly
Monitoring
Inspection
Daily
Daily
Daily3
DailyS
Daily3
Daily
Daily
Weekly
Daily
Daily
Equipment
Service
1
1
1
1
1
1
1
1
1
Emergency
Systems
Alarms Waste Cutoff
-
Weekly
Weekly
Weekly
Weekly
Weekly
Weekly
' " - • .
Weekly
Weekly
-
Weekly
Weekly
Weekly
Weekly
Weekly
Weekly
•••-•'
Weekly
Weekly
  1 Equipment manufacturer's recommendation.
  2 Equipment manufacturer's recommendation or no less than monthly.
  2 Operators are also alerted immediately as to the functionality of the instruments because of the  continuous monitoring response of this
   equipment
Table 6-2.    General Maintenance and Troubleshooting of Incinerator and Auxiliary Equipment
 Equipment
          Indicators
            Problems
      Recommended Maintenance
          and Troubleshooting
 Incinerator refractory    Excessive temperature
 Chamber pressure

 Chamber excess Og

 Liquid/slurry/sludge
 waste feed system
 Solid feed mechanism
Excessive pressure
(high Or low)
Excessive Oa; unresponsive
to firing  rate
Excessive variations in Q%
and CO
                       Excessive variations in waste
                       feed pressure at the burner
Excessive variation in 02,
temperature, CO, and/or
pressure
• Loss of refractory, corrosion
• Flame impingement

• Ash deposit, plugging
• Excessive flowrate
• Excessive air leakage
• Obstructed fan dampers
• Variable waste concentration and
  heating value
• Excessive feed rate
• Feed line plugging

• Feed line plugging
• Excessive solids in  the waste
• Improper preheating of waste
                                                        Pump problems
                                                        Loss of atomization fluid
                                                        (air-steam)
• Feed conveyor problems
• Feed ram cycle timer
• Hydraulic feed system
• Blockage of screw feeder
  Inspect and replace. Review refractory
  specifications.              ..-..,
  Nozzle erosion. Inspect and replace.
  Inspect chamber, transition ducts,
  APCE indicators
  Inspect combustion air control System,
  fan and dampers           .
  Inspect seals and air fan dampers and
  control mechanism    .
• Inspect mixing tank and recirculation
• Adjust feedrate
• Inspect feed line screens, filter for
  deposits, plugs

• Adjust temperature control for waste
  viscosity
• Inspect waste pump operation
• Inspect atomization air blower, steam
  supply
• Inspect solid feed system for timing,
  blockage and proper operation of
  components  •
                                                              80

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Table 6-3.   General Maintenance and Troubleshooting of Air Pollution Control Equipment


  Equipment	Indicators	Problems	
                                                                    Recommended Maintenance
                                                                       and Troubleshooting
 Quencher
Erratic outlet temperature
 Venturi scrubber
 (conventional and
 IWS)
                      Consistently high outlet
                      temperature
Erratic pressure differential
 Absorption scrubber    Surging pressure differential
 Fabric filter
Excessive pressure differential
 Electrostatic
 precipitator
Excessive sparking rate

Intermittent smoke "puff"
• Partially plugged nozzles
• High variation in Incinerator
   moisture feed
• Low gas flowrate (< 30 fps)
• Water droplet impinging on
   thermocouple

• Plugged nozzles
• Low water flowrate and high
   temperature   '     •
• Excessive gas speed (> 50 fps)
• Plugged nozzles
• Adjustable throat diameter is too
   wide
  Face velocity in excess of 12 fps
  Plugged tray sections
  Nonuniform scrubber liquor
  distribution
  Leaking seals
  Localized plugging of packing
  Hole in the packing
  Excessive gas flowrate
  Bag blinding (high dust loadings)
  Leaking air lock or dampers
  Faulty cleaning mechanism
  Excessive dust accumulation in
  clean side of bags
• High moisture in gas
• Excessive voltage and current
  settings

• Improper sampling or cleaning
  frequency
• Poor incinerator operation
• Overload of ash hoppers
• Inspect and replace plugged nozzles
• Control moisture feed to incinerator

« Increase gas flowrate to design range
• Relocate "thermocouple, replace
   defective nozzles

• Inspect and replace plugged nozzles
• Calibrate water flowmeter; adjust to
  '50-80 percent of evaporation loss
• Reduce pas flowrate
• Inspect headers, flanges and nozzles
• Reduce throat diameter and adjust liquid
   flowrate
• Inspect throat regularly for deposits and
   wear
• Inspect spray nozzles, water flowrate,
   weir bozes, seals, and downcomers for
   proper operation.

• Inspect packing, adjust caustic.
   conecntration to 15-20 percent.

* Reduce gas flowrate; check bleed air
• Inspect cleaning mechanism; replace
   bags
•  Check proper temperature of gas to
   prevent condensation
•  Inspect proper removal of collected ash
   from hoppers
•  Reduce moisture feedrate
• Adjust setting assembly
• Adjust rapping cycle

•  Inspect waste feed to incinerator
•  Inspect hopper for excessive deposits
6.2 Safety and Waste Cutoff Interlocks
The  operating  permit  should  also  specify  that  all
alarms,  automatic   waste  cutoff  systems,   and
emergency shutdown  interlock  systems be routinely
checked to verify  operational status. This  I&M activity
is particularly  critical  to the operation of  the facility
because the failure to interrupt  waste feed during  an
operational  upset could   result  in  a  dangerous
                                        situation.  Therefore, and as  required  under 40 CFR
                                        264.347(c),  all  automatic waste  feed systems  and
                                        associated  alarms  should  be  tested  on at  least a
                                        weekly basis. Checking at a lesser frequency, up  to a
                                        monthly basis can be allowed if adequate and if more
                                        frequent  testing  can  be  shown  to  unduly  upset
                                        operation.
                                                                                                                                   m

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                                          APPEND1XA
                                Sources of Further Information
This document is part  of  the Hazardous Waste
Incineration Guidance Series prepared by the EPA to
assist both the applicant and the permit writer  in the
RCRA process leading to a final operating permit for
hazardous waste incinerators.
Hazardous Waste Incineration Guidance
Series

Volume I

    Guidance  Manual for  Hazardous  Waste
    Incinerator  Permits. Mitre  Corp. NTIS  PB84-
    100577. July 1983. (Document is  scheduled for
    revision.)  Describes the  overall incinerator
    permitting  process, highlights  the  specific
    guidance  provided  by other  manuals,  and
    addresses  permitting issues not covered in  the
    other manuals such as treatment of data in lieu of
    trial burn.  Thus, it can be viewed as a road map
    and a good summary of all permitting issues.

Volume II

    Guidance  on Setting Permit  Conditions  and
    Reporting  Trial Burn Results. Provides guidance
    to the permit applicant on reporting trial burn data
    and to the  permit writer on  translating these data
    into  meaningful  and enforceable  operating
    conditions for incinerators. Acurex Corp. 1989.

Volume III

    Hazardous  Waste 'Incineration  Measurement
    Guidance  Manual. Midwest Research Institute.
    1988.  (Draft under  EPA  review.) Addresses
    monitoring,  sampling,  and  analytical
    instrumentation and the test methods required for
    trial  burn  testing  and  enforcement  activities.
    Sampling  and analysis  methods  for multimedia
    emission   evaluations  including  quality
    assurance/quality control are also discussed.

Volume IV

    Guidance  on Metals and Hydrogen Chloride for
    Hazardous  Waste Incinerators.  Versar,  1989.
    (Draft under EPA  review.) Specific guidance on
    limiting metals emissions  from  incinerators   is
    provided.    In  particular,  a  risk assessment
    approach to setting limits on  metal components
    inthe  waste  is  employed.  Guidance is also
    provided  on  doing  risk-based checks on  HCI
    emissions. (NOTE: Earlier title was: Guidance for
    Permit Writers  for Limiting  Metal  and  HCI
    Emissions from Hazardous Waste Incinerators.)

Volume V

    Guidance on PIC Controls for Hazardous  Waste
    Incineration. Midwest  Research Institute.  1989.
    (Draft under  EPA  review).  Details the specific
    permit requirements for CO and total hydrocarbon
    (THC) emissions from  hazardous  waste
    incinerators in the RCRA system.  Emission limits
    for CO  and  THC  and the  rationale for their
    selection are discussed. (NOTE: Earlier title was:
    Guidance  on Carbon Monoxide  Controls  for
    Hazardous Waste Incineration.)

Volume VI

    Proposed Methods for Measurement of CO,  Oz,
    THC,  HCI and  Metals  at Hazardous  Waste
    Incinerators. 1989. Presents a draft measurement
    method  for the above  parameters  including
    performance  specifications  for continuous  CO
    monitors.
Other Reference Documents

1.  Engineering Handbook  for Hazardous  Waste
   Incineration.  EPA  Publication  SW-889.
   September 1981.

2.  Practical  Guide - Trial Burns for Hazardous
   Waste Incinerators.  Midwest Research Institute.
   EPA  Publication No. 600/2-86-050.  1986

3.  Trial Burn Observation Guide. Midwest Research
   Institute. 1988. (Draft under EPA review). Includes
   general  guidance  on preparation,  on-site
   activities,  and  reporting aspects of observing  a
   trial burn test.
                                               83

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4.  Background  Information on  Sampling and
   Analysis Methods Related to the Amendments to
   the Incinerator Regulations and to the Regulations
   on Bo'lers  and Industrial Furnaces.  Midwest
Research  Institute.  1988.  (Document  under
preparation.)  Includes  descriptions  of
recommended sampling and analysis methods.
                                             84

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                                            APPENDIX B
                             Guidance For Incinerator Design Review
During the process of permitting  a hazardous waste
incinerator, the permit writer must make a number of
engineering assessments. Before approving the trial
burn, the  permit writer  must be  assured that the
design is adequate to protect human health and the
environment. After  the  trial  burn, the permit writer
must be assured that  the trial  burn data  are
consistent and believable and that the data  can be
properly  interpreted  to  establish  a flexible  set  of
permit conditions  which are  in  compliance  with
performance standards.  This  appendix  gives  the
permit writer background on incinerator design so that
an application is reviewed to:

1. Ensure that  there are  no major  design flaws  of
  sufficient magnitude to render a trial burn unsafe"
2. Ensure that  the trial  burn will  generate sufficient
  verification information so that trial burn data may
  be propeny interpreted and evaluated

In pursuit  of the  first objective,  the permit writer
should remember  that  the   key  phrase  is  "major
design flaws."  Incinerator design information available
to the permit writer  is not so universally applicable
that  a prior prediction  of incinerator performance
could be made with confidence;  otherwise, there
would be no need for trial burns. An example of a
major design flaw would be  an  incinerator  that  is
predicted to operate 200°C  (390°F) lower than  its
design temperature  but has  inadequate auxiliary  fuel
provisions to make up the difference. An example of a
minor design flaw is an incinerator that is predicted to
operate  200°C (390 °F) hotter  than  its  design
temperature.

The  design  review is  most  applicable to  new
incinerators which must be permitted before they  can
be built.  For existing  facilities, one  can generally
determine  from observation  of  the unit or from
operating data that it can attain specifications such as
trial  burn temperature  and  sufficient quench water
flow to achieve the desired APCE temperatures.

The permit writer should  perform the following steps
for a design review:

1. Review the  overall  facility design and  system
  schematics
 2. Review thermal treatment equipment design

 3. Estimate temperature and gas residence time and
   verify  other  control  parameters  for  internal
   consistency

 4. Review APCE design and estimate efficiency
 5. Review  measurement  techniques  and safety
   interlocks

 6. Consider special wastes and similar systems


 B.1 Overall Facility Design
 A schematic diagram  of  the  incineration system
 should always be reviewed by  the  permit writer. All
 waste, fuel, air,  water, and other input streams as well
 as the locations of all required measurement, should
 be labeled  on the diagram. The permit writer should
 determine if all  components of the system are being
 taken into account and that the permit parameters are
 being  set  and monitored  with the  proper
 measurements.

 Figure B-1  provides  layouts  for  typical  incinerator
 facilities. For the most  part,  these  facilities can  be
 viewed as  straight-through systems  in which wastes
 are incinerated  in single or multiple chambers with
 further thermal  and  flue  gas  treatment  occurring
 downstream. The layout at the top of the figure shows
 a typical facility where the combustion gases leaving
 a  PCC such as a  rotary kiln or  liquid  injection
 chamber are further treated  with a SCC,  which is
 sometimes called an afterburner. Frequently, the SCC
 is fired  with a liquid  organic  waste  instead  of fossil
 fuel. This practice is  quite common as  it results in
 significant cost reductions.

 In most cases, flue gas  scrubbing for particulate and
 acid control is  required  to  meet current  emission
 standards.  It is  important to point  out that  some
facilities do not use afterburners nor  APCE. For these
 units, operation  is considerably simplified,  but they
 are restricted to  burn essentially ash-and  halogen-
free  wastes to  comply with  RCRA  standards for
 particulate and acid emissions.

 Some commercial facilities use two  PCC units,  each
designed to incinerate  a category  of wastes; for
                                                 85

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r
               Figure B-1   Incinerator equipment arrangements.
'1
L ^


r*


Primary
Chamber
(PCC)





A


— I/
r*


Secondary
Chamber
(SCC)








APCE

                                                                                                       Stack
                               Pumpable
                                                    Pumpable
                                               Ash
                                   V
                                 Residue
                                        Primary
                                        Liquid
                                        Chamber
                                        (PCC)
                                                                               Residue
                                                                                                      Stack
                           Solids
                           Sludge
                           Slurries
Ash
   A-Combustion air
   F-Primary fuel
APCA - Air pollution control
       equipment
               example, liquids  in a  liquid  injection  chamber  and
               solids/sludges  in  a rotary  kiln.  These  facilities  are
               designed for maximum  waste  flexibility and operation.
               The  combustion  gases  from  both chambers  are
               ducted  to  a  common  SCC  unit for  complete
               incineration  of remaining  combustible  byproducts
               before  scrubbing  for  paniculate  and  acids  takes
               place.

               One  other  design variation, especially for  large
               commercial incinerators, is heat recovery using  waste
               heat  steam  generators or  boilers.  This  equipment,
               which is always found upstream of APCE, is typically
               a "passive" device  where no  supplemental  firing
               occurs. Therefore, it requires little or no consideration
               on the part  of the permit writer in  setting  operating
               permit conditions.  However, in the case where  the
               boiler is supplementary fired,  the permit writer should
               consider its  operation as a  tertiary  combustion
               chamber where further waste destruction occurs.
                      B.2 Incineration Equipment
                      There  are a number of different types of incinerators
                      and many design variations for each type. The permit
                      writer should realize, therefore, that no single design
                      review  tool  is  universally  applicable.  Thus, it  is
                      important for  the permit  writer to  know the basic
                      principles of  incineration  to  perform a  "best-
                      engineering"  analysis  of  the  design.  Towards  this
                      aim, this section reviews the principal design features
                      of  thermal  treatment equipment and  specifically
                      provides review guidance  for design  factors deemed
                      most important to incinerator performance.

                      As mentioned, incineration of hazardous waste  can
                      be accomplished  by  several  types of  high-
                      temperature combustion devices. Some of these have
                      a  rather  long operating  experience,  other more
                      recently developed types  are  not yet in widespread
                      use, while still others  are currently  under research
                      and development. By far the most common
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 incineration devices  or PCC units  are  the  liquid
 injection chamber,  rotary kiln, and  fixed hearth.  The
 discussions below  focus on these  three principal
 designs  that comprise well  over 80  percent of the
 estimated  221  incinerator facilities  already permitted
 or  operating  under  interim  status  (1).  The  total
 thermal capacity of these units is projected at about
 650 MW (2,200 x 1Q6 Btu/hr) or 93  percent of total
 incinerator capacity.  Table  B-1  summarizes  major
 design  features, typical operating  characteristics,
 suitable wastes,  and  other  general  information
 pertinent to these  incinerator types.  For the reader
 interested  in obtaining additional  information,  Kiang
 and  Metry  (2)  and  Bonner,   et al,  (3)   are
 recommended  as guides. Other  information  can  be
 obtained directly from incinerator manufacturers.

 A section on  fluidized  bed  combustor  (FBC)
 incinerators is  also presented below. These  units,
 which represent less  than 3 percent  of  the  existing
 population, are not specifically treated in this permit
 guidance because  of  specific design and operating
 considerations  and the  inadequate  data base on
 performance characteristics.

 B.2.1 Liquid Injection Incinerators
 As the name implies, a  liquid injection incinerator is
 designed  to burn  liquid or  pumpable  hazardous
 wastes. The refractory chamber is typically cylindrical
 and  is  oriented for either down-firing or  horizontal
 firing. The  primary  consideration  in the  selection of
 the firing orientation is the amount of inorganic ash in
 the waste and its chemical composition. Waste with a
 significant  quantity of  inorganic  salts  is  typically
treated  in a  down-fired  system.  At the  high
temperatures required for  waste destruction, these
 salts are liquified; they may adhere to the refractory
 and form a slag. Removal of the molten slag in  the
 down-fired  liquid  injection  chamber is aided  by
gravity.  However,  in  a  horizontally-fired  chamber,
this  gravity-assisted slag removal  is not  possible,
and  deposits  of successive layers  of  ash often
 accumulate on the  lower  part  of  the chamber.
 Because these  increased ash deposits can effectively
 reduce  the available  chamber volume,  lower  gas
 residence times and  reduced gas mixing,  increased
 maintenance, and reduced firing capacity can result.
 For example,  for  a  260-KW/m3  (25,000-Btu/hr-cu
ft) liquid injection chamber fired with liquid  waste
containing  5  percent  alkaline  salts  and  low-melting-
point metal oxide ash, the accumulation of slag in the
chamber could  be  as much  as 15  percent of its
volume  for 100 hr of operation.  For these cases,
 routine visual inspection combined with practical limits
on  ash content  for  horizontally-fired   liquid
incinerators should be considered by either the facility
operator or the permit  writer.
Liquid injection incinerators  can  be  fired  under
positive (forced draft) or negative pressures (induced
or balanced draft systems).  Typically,  positive-
 pressure chambers are used unless the facility  is
 equipped with APCE.  Because high-efficiency  APCE
 often results in high pressure drops, a balanced draft
 (forced draft-plus-induced  draft  (FD  plus ID))
 system is often used.  This configuration prevents the
 PCC unit  from operating  under  excessive  positive
 pressure to overcome flow  restrictions in the APCE.
 To maintain  the  proper  pressure  in the chamber  is
 important for equipment  safety as  well as for fugitive
 emission control considerations.

 Pumpable  liquid waste is injected into  the  chamber
 through  atomizing  burner  nozzles.  The liquid  feed
 system should be properly designed to avoid feed line
 plugging,  excessively variable feed composition,
 nozzle  erosion,  and  poor  atomization.  A  good,
 commonly used method of minimizing these problems
 is the use of waste recirculation at the tank and  at the
 burner.

 Other  desirable  designs  include multiple  burner
 arrangements which allow better waste distribution in
 the  chamber,  more  efficient atomization,  and
 improved  turndown firing  capability.  Preferably,
 primary  combustion  air  should be injected  at each
 waste  burner location  to provide  stable combustion
 with rapid  droplet vaporization and  burnout.  Waste
 heating value  is not critical when supplementary fuel
 (waste or fossil fuel) is available to maintain chamber
 temperature.  For  high-water-content  waste, the
 feed rate should not be  too high to prevent  primary
 flame quenching,  which can  be manifest in increased
 CO  and hydrocarbon  emissions.  The  design and
 operating practices  are also important for SCC units
 or  afterburners because  liquid   wastes are  also
 incinerated in these  devices.

 A key factor  in the performance  of liquid  injection
 incinerators is atomization quality, which is defined by
 the  droplet  size  distribution  of  the  spray.  The
 presence of large drops cannot be tolerated because
 if  the  residence  time  in the combustion zone  is
 insufficient to ensure complete combustion, unburned
 material may exit the combustion chamber.

 Nozzles are  typically either internal  or  external
 atomizing and mechanical or twin fluid. The difference
 between an  internal and external atomizing nozzle
 relates  to the  point in the  nozzle  where the  fluid
 (waste or fuel) is atomized. While this  difference  is
 important in the design and selection of the nozzle,  it
 is not  important  in  the evaluation  of a  permit
application. Mechanical or twin fluid atomizing nozzles
are generally  employed in liquid injection incinerators.
 One common type of mechanical atomizer is a simple
pressure jet in which the liquid is forced through  a
constriction;  atomization occurs  because  of the
 instability of the liquid film formed downstream of the
constriction. Droplet size increases  with  increasing
liquid flow and decreasing hole size.  Another  type of
mechanical atomizer is the rotary cup  in which   a
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Table B-1.    Incineration Equipment

 Equipment Type	Typical Design Features
  Suitable Wastes
       Other Considerations•
 Liquid Injection    •  Refractory-lined furnace down- or
                   horizontally-fired
                 •  Positive pressure or balance draft design
                 •  Heat input capacity of 0.37-38 MW(0.125-
                   130 x 10s Btu/hr)
                 •  Typical L/D = 2 to 3:1
                 •  Heat release rates of 100-370 KW/m3
                   (10,000-35,000 Btu/hr-cu ft)
                 •  Operating temperatures of 980-1,650°C
                   (1,800-3,000°F)
                 •  Gas residence times of 0.3-2 sec
 Rotary Kiln       •  Refractory-lined cylindrical rotating furnace
                   mounted horizontally with a slight incline for
                   passage of ash
                 •  Negative pressure in the kiln
                 •  Heat release rates of 160-470 KW/m3
                   (15,000-45,000 Btu/hr-cu ft)
                 •  Operating temperatures of 650-1,260°C
                   (1,200-2,300°F) for PCC; 800-1,600°C
                   (1,470-2,800 °F) for SCC
                 •  Gas residence times of 1-3  sec (in SCC)
                 •  L/D of 1:5 for kiln
                 •  Variable rotational speed typically in the
                   range of 0.01-1 rpm
                 •  Solids retention time of 1 -2  hr
                 •  Solids waste feed capacity 0.17-0.56 kg/s
                   (1,300-4,000 Ib/hr)
 Fixed Hearth      •  Single or multiple refractory chambers
                 •  Typical waste loading capacity 0.05-0.3
                   kg/s (400-2,400 Ib/hr)
                 •  Heat capacity 0.9-5.3 MW (3-18 x 106
                   Btu/hr)
                 •  Underfire and overfire air injection designs
                   available
Primarily pumpable
and atomizable liquid
wastes
Low- and high-
heating value wastes
Halogenated wastes
Organic vapor-laden
waste gases
Solid, liquid, and slurry
wastes
Contaminated, bulk
low- or high-heating
value wastes
Suitable for gaseous
wastes    .         .
Primarily solids and
sludges
Low- and high-
heating value wastes
Halogenated wastes
Supplemental fuels are required for the
initial refractory heat-up period and for '
incineration of LHV wastes       •
Typically operating with excess air from
combustiori blower
SCC not always necessary
Supplemental fuel is required for the
initial heat-up period and for.   .,
incineration of low heating value wastes
Considerable retention time of solids is
required  •
SCC is required with pyrolytic or excess
air combustion       .
Supplemental fuel is required for the
initial heat-up period and for
incineration of LHV wastes
Typically used for treatment of small
quantity of wastes
PCC can be operated with both excess
or starved air
liquid  jet  is  impinged on a spinning cup  or disk.
Centrifugal forces cause  the  resulting  droplets  to
move  radially outward, and  the combustion air flow
must be  used to  direct the  droplets  into a favorable
path for  combustion  within  the incinerator  chamber.
Rotary cup  atomizers are  used  for sludges and
slurries because they do not have narrow  passages
that can  be  plugged. In the  twin fluid  atomizer,  a
second fluid, either  high-pressure steam  or  air,  is
forced  at high  pressure  and  velocity into  a  slower
moving liquid jet,  and atomization  occurs because of
the  high   shear  between  the  two streams.  These
nozzles can produce extremely fine drops if sufficient
atomization fluid is employed (4).

The permit  writer should  compare the liquid  waste
burner specifications with the quantity and  properties
of the  waste to be burned to  ensure the following:
•  The burner  is  the  appropriate size to handle the
   range of waste  flows expected.

•  The viscosity of the waste as fired is not too  high.

•  The particle size and quantity of solids in the waste
   are  not too high.
 B.2.2 Rotary Kiln Incinerators
 Rotary kilns are refractory-lined cylindrical chambers
 positioned with  a slight incline  from  the horizontal
 plane. The rotation of the kiln promotes the mixing of
 the solid  waste and  hot  combustion  gases  and
 transports the ash down the length of the chamber to
 the ash  hopper. Incinerator facilities  utilizing  rotary
 kilns  provide the  greatest  flexibility  for hazardous
 waste disposal. The kiln can accommodate a variety
 of  solids,  slurries,  and  sludge  waste  streams in
 containerized form such as fiber packs and drums or
 as bulk or shredded solids. In addition, the rotary kiln
 operates  as  a  liquid  injection  unit because  liquid
 wastes are also injected through atomized waste feed
 burners.  Existing rotary kiln  capacities range  as high
 as 44 MW (150  x 1Q.6 Btu/hr), and larger .commercial
 facilities  are  under construction.  Chamber  operating
 temperatures are typically below  1,090°C {2,000°F),
 with many units  operating  with exit gas temperatures
 aslowas650°C(1,200°F).

 Several factors should be scrutinized when rotary kiln
 designs  and  trial  burn  data are  reviewed.  Waste
 devolatilization,  ash  retention time,  and .paniculate
 entrainment  have  a  strong   influence  on  the
                                                        88

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performance of rotary kilns and snould be considered,
or computed, as follows.

Waste Devoiatilization
Wastes are generally fed to kilns in batches, often in
disposable drums  that cause  cyclical  transient
behavior. When a batch first enters the kiln, it heats
up,  dries, and  devolatilizes, consuming heat  and
cooling the kiln. Then  the volatiles burn very quickly;
the  rate is limited  only by  turbulent mixing and  the
availability of oxygen. The rapid burning can cause a
rapid increase in gas temperature and decrease in  the
excess air level.  These transient effects  of  batch
feeding  become more pronounced with  increasing
charge size, volatile  content, and kiln  temperature.
Kilns are generally run at  high excess air levels (often
100 percent or  more)  to allow  for these transients.
After the  volatiles are released  and  burned,   the
remainder of the  heat content  of the  waste  burns
relatively slowly.

Ash Retention Time
Kiln ash  retention time is  inversely proportional to  kiln
slope and rotational speed and is directly proportional
to the length-to-diameier ratio.  It may be estimated
according to the U.S. Bureau of  Mines (1927) formula
(5):
                 6^0.19L -8- NSD

where:

  8  = Ash retention time, min
  L  = Kiln length, m
  D  = Kiln diameter, m
  N  = Kiln rotational speed, rpm
  S  = Kiln slope,  m/m

Participate Entrainment
Particulate  entrapment  in  a rotary  kiln  depends
primarily  on the size and density of the solids,   the
velocity and properties of the gas, and kiln design and
operating conditions. The  subject has been treated by
Khodorov (1961) and by Li (1974) (6):
      w =
                           ,J/2
where:

  W    = Entrapment rate, kg/s
  K£   = Proportionality constant which  varies with
          the roughness  between  the cylinder wall
          and feed solid
  D    = Inside diameter  of the cylinder, m
  F    = Solid feed rate,  kg/s
  N    = Cylinder rotation speed, radians/s
  S    = Cylinder slope, m/m
  6    = Dynamic angle  of repose  of the  solid,
          radians
  U    = Gas velocity,  m/s
  p    = Gas viscosity, N s/m2
   p    = Gas density, kg/m3
   d    = Solid density, kg/m3
   Ds   = Diameter of the feed particles, m
   n    = Solid particle size distribution parameter .
   f(Cf) = Modification parameter, which is a function
          of the concentration  of entrainable fines in
          the solid

 Incineration  of bulk  solids  and  containerized
 hazardous wastes  requires  special  considerations.
 The complete burning of solid combustible material
 requires longer residence times  than  liquid and gas
 waste  fuels. The length of time, which can be as long
 as 2 hr, depends on the rate of the mass transfer of
 the organic  component in the solid waste to the gas
 stream. The rate of mass transfer, in turn, depends
 on  temperature,  the  size of the  solids, the  volatile
 content of  the waste, and  the  degree of  mixing
 achieved. The  rate  of  solid feed,  the  size  of
 containerized  solid waste, the solids  loading in the
 kiln, and  the retention time of  ash in the kiln are all
 important considerations  for  achieving  complete
 combustion  of combustible  material  while  retaining
 sufficient  efficiency  to destroy  volatilized  POHCs.
 Although  current RCRA  regulations do  not address
 incinerator  residue  quality  (i.e.,  the degree  of
 complete  combustion  of  the ash  leaving   the  kiln),
 many  States  and local  regulatory agencies  require
 that the incinerator operate in  a  manner that  avoids
 creating an  ash  disposal  problem. This requirement
 imposes routine  analyses of the residual  ash, with
 further treatment  if necessary, before landfill disposal.

 Rotary kilns can  operate with excess combustion  air
 or under pyrolytic  or oxygen-starved conditions.
 Typically,  excess air  is  used,  thus providing  an
 oxidizing  environment  which  is generally  more
 protective of  refractory  material.  Irrespective  of
 excess air levels, the combustion  gases   generally
 pass  through  a SCC or  afterburner to  ensure
 complete  combustion of  measured organics leaving
the kiln unit. For a rotary kiln burning a variety of bulk
 solids, secondary  incineration  of  combustion
 byproducts is  more critical  to  efficient destruction
than a liquid  injection incinerator.  Typically,  SCC
 chambers for  rotary  kiln  systems are  conservatively
 designed  to  provide  high  temperature  and  longer
 residence times. Also, most rotary kilns operate under
 negative  pressure for control  of fugitive emissions
from waste feed areas and kiln end seals during ash
removal.  Air  pollution  control  is  inevitably  required
with  this  incineration  system due  to  the  nature  of
hazardous waste treated.

 8.2.3 Multiple Hearth Incinerators
A multiple hearth incinerator typically consists  of a
series  of flat hearths within a refractory shell. Sludge
or solid waste is continuously  fed through  the roof
onto the top hearth. Rotating arms cause the waste to
drop from hearth to hearth until the remaining ash is
discharged at  the  bottom  of  the  furnace.  Air  is
                                                   89

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 preheated as it  is used  to  cool  the  rotating  arms.
 Additional heat is provided through auxiliary burners.
 Gas flows countercurrent to the waste and  exits at
 the top of the furnace.

 Existing multiple hearth incinerator  designs  have  a
 heat input capacity of 0.9 to 5.3 MW (3 to 18  x  1Q6
 Btu/hr). Each chamber is typically equipped with oil or
 gas burners for startup  and  supplemental  heat
 requirements. For larger incinerators with  capacities
 greater than 93 kg (200 lb)/hr, solid waste feed and
 ash  removal  are  automated  with  hydraulic-
 ram/hopper  or cart-dumping  systems.

 As with rotary kiln incinerators,  the  factors of waste
 devolatilization, ash retention, and entrainment should
 be considered. Waste bed combustion on the primary
 chamber grate  is typically accomplished  at low
 temperature  and with  a minimum  of underfire  air to
 prevent  formation  of  metallic  salts and  minimize
 particulate emissions.  Solid waste-charging systems
 are designed so  that  volatiles  from "fresh"  waste
 pass  through the flames in the  flame  port before
 entering the  mixing chamber. The rate  of ignition of
 unburned solid waste containing high concentrations
 of volatiles  (including  moisture) is maximized  using
 small waste  feed batches.  This operation prevents
 flash  volatilization,  which carries  the potential  for
 flame quenching and  smoke generation. Controlled
 waste charging also reduces the need for bed stoking
 required at times to enhance solid waste burnout.

 Solids transport is determined by the rotational rate of
 the rabble arms and the location of the drop holes.
 Entrainment  can occur as  the waste drops  from
 hearth to hearth if the opposing gas velocity is greater
 than the terminal velocity of the  waste  particles.
 Entrainment  increases with increasing  gas flow and
 with decreasing particle size and density:

 B.2.4 Fluidized Bed Incinerators
 Although  fluidized bed incinerators  or combustors
 (FBCs)  represent a minor fraction  of  the  existing
 waste  incinerator population,  several  design  and
 operating advantages of these units are likely to result
 in increased use  of these equipment types in the
thermal destruction of hazardous  waste. The FBCs
are typically  simple, compact combustors that provide
efficient destruction of a wide variety of wastes (i.e.,
solid,  liquid,  and gaseous) at low temperature.  The
 main chamber consists  of a  bed of hot inert material
which is fluidized  with 0.76 to 2.4 m/s (2.5 to 8.0 fps)
combustion  air.  Bed temperature  is  typically
maintained in the range of 450 to  850°C (840 to
 1,650°F). Waste incineration occurs in and above the
bed (freeboard area) where  temperatures can reach
980°C (1,800°F). The bed material can be selected
to maximize  retention of halogenated acids  and
metallic oxides, thus reducing the emission burden to
the APCE. For several FBC designs, a high residence
time of  liquid and solid waste  in the  hot bed  is
 achieved.  Circulating bed combustors (CBCs) are
 designed for increased reentrainment of solids in the
 gas stream leaving the chamber. The solids are  then
 captured  in a  downstream  cyclonic  hopper  and
 reinjected  into the PCC. This CBC design essentially
 extends the  bed  volume  to the  entire primary
 chamber  in comparison  with  conventional  FBC
 design.                           -       ._.., .

 Aside from temperature, the primary design factor  to
 be considered is the gas velocity, which must be  high
 enough to  maintain bed fluidization but low enough  to
 prevent bed attrition. It is constrained by the terminal
 velocity  of the  bed particles and  is, therefore,  a
 function  of the particle size.  Superficial velocities  in
 the range of 1.5 to 3 m/s  (5 to 10 fps) are common.
 Entrainment from  a fluidized bed  occurs  when the
 terminal velocity of the waste (or bed)  particles is  less
 than the velocity of the gas  in the freeboard space
 above the  bed. Entrainment increases with increasing
 gas flow  and  with decreasing  particle  size  and
 density.
 B.3  Temperature  and  Gas  Residence
 Time
 Incinerators allow  for the destruction  of  hazardous
 wastes  by providing high  temperature  and sufficient
 time in an oxidizing environment for the waste to burn
 such  that harmless or easily removed products such
 as 02, H2O, HCI,  and ash remain. The permit writer
 should perform specific calculations  to determine if
 the temperatures and gas residence times reported in
 the trial  burn plan are  reasonable  and  can  be
 expected to be demonstrated in the trial burn.

 B.3.1 Calculation Technique
 This  section presents a  technique by which  the
 permit writer can calculate the temperature and  gas
 residence time in the combustion  chamber of  an
 incinerator using the waste feed  and design data as
 presented in a permit application. It should  be kept in
 mind  that every  incinerator  is  unique  and  that
 application  of this generalized  technique to a
 particular incinerator may  be  inaccurate.  When
 possible,  a  detailed energy  and   mass balance
 (E&MB),  as  described in Appendix E,  should  be
 performed. An  E&MB is capable of computing  not
 only both temperature  and residence time but also
 many operational parameters.  It can,  therefore,  be
 used  as  a tool to  verify information  developed from
 the trial  burn itself.  Nevertheless,   generalized
 correlations  such  as those presented in this  section
 are useful to illustrate trends and to extrapolate data
 over a limited range.

 Residence time  and effluent flow  in an  incinerator
 largely depend on  total air flow to the  incinerator. A
fair approximation  of residence time can  be made
                                                  90

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using the ideal assumption that only air flows through
the incinerator, resulting in equation 1:
                                            Figure B-2.  Actual-to-ideal residence time ratio  vs.
                                                       moisture-to-air mass flow ratio.
where:

   ^ideal
   V
   P
   mair
                                              (1)
= Ideal incinerator residence time, s
= Volume of the combustion chamber, m3
= Pressure of the combustion chamber, atm
= Total flow of all air including leaks into the
  combustion chamber, kg/s
= Combustion chamber temperature, °K
This approximation can be made because most of the
volumetric throughput in an incinerator is due to air
and  because combustion of  most fuels  and wastes
produces  about the same number  of  moles  as  it
consumes.

When  the  waste has  a high aqueous or  moisture
content or when a significant  water stream is fed into
the  incinerator,  equation  1   tends  to  overpredict
residence time, and  a  correction  factor  must  be
applied. Figure B-2   shows  the  value  of  this
correction factor as a  function of the mass ratio of
water to air  flows to the incinerator, where the water
flow includes  the  sum of  all moisture   content,
aqueous content, or water in  all  streams  input  to the
incinerator, and the air flow includes the sum of all air
flows including  leaks.  For  incinerators  in series,
residence time of the  first unit  would  be calculated
from all air and  water flows into that unit alone, but
residence time  of each succeeding unit would  be
calculated from all air and  water flows into  that unit
and  all units upstream. Residence time  can  be
converted into actual volumetric flow in actual cubic
meters per second by equation 2:
             Volumetric flow = V •*•
                                     (2)
or to velocity (U) in m/s by equation 3:

    U = Volumetric flow -s- Cross-sectional area  (3)

where cross-sectional area is in m2

Temperature  in  an  incinerator  can  be  roughly
correlated with the fractional heat loss and the ratio of
total heat  input to total mass  input,  as shown in
Figure  B-3. This  correlation assumes  that the heat
capacity of a  combustion mixture  is independent of
composition,  which  is  a reasonably  accurate
assumption unless  the  mixture has a  high  water
content. Figure B-4 shows the correction to the ideal
temperature that must be applied to account for water
content.
Fractional heat loss is the ratio of heat loss through
the walls to total heat input to the incinerator.  It is a
function of temperature, size,  shape, insulation, and
                                                      0)
                                                      ir
                                                      <»
                                                      -Q
                                                          1.0
                                                 0.8
     0.6
                                                 0.4
                                                 0.2
                                                                   l
                                                           0.2      0.4     0.6     0.8

                                                           Moisture Mass Flow/Air Mass Flow
                                                                                          1.0
                                            heat input.  Most hazardous  waste incinerators are
                                            fairly well-insulated  and have  a fractional heat  loss
                                            of less than  10 percent.

                                            The total heat input to the system includes the sum of
                                            all chemical and sensible heat inputs as shown in
                                            equation 4:
                                            Total Heat Input
                                                =  2 Chemical Heat Input
                                                +  S Sensible Heat Input
                                              (4)
The chemical heat input from a fuel/waste stream  is
the product of its mass flow and lower heating value
(LHV) as calculated in equation 5:
     Chemical Heat Input =
                                                                                 x LHV   (5)
                                            Because only the higher heating value (HHV) of a
                                            fuel/waste is typically measured, the LHV  may  be
                                            approximated from equation 6:

                                            LHV = HHV - [(1-MOISTURE)HFAC + MOISTURE]  2,440
                                                   - Cl  (1 - MOISTURE) 1,160
                                                                                         (6)

                                            where both  LHV and HHV  are in units of kJ/kg and
                                            where MOISTURE is the mass fraction of liquid water
                                            in the fuel/waste, Cl is the mass fraction of chlorine in
                                            the dry  fuel/waste,  the combustion  water parameter
                                            (HFAC)  is the ratio of the  mass of water generated
                                            from the combustion of hydrogen in the fuel/waste to
                                            the mass of  the dry fuel/waste and 2,440 kJ/kg (1,060
                                            Btu/lb) is the heat of vaporization of water. The final
                                            term in  equation  6 is  not  normally  seen in the
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 classical definition of lower heating value, but is used
 to  account for  the  fact that in  most heating value
 measurements,  the ^chlorine comes  out  in  solution;
 1,160 kJ/kg (500 Btu/lb) is the heat of solution of HCI.
 Figure B-5 shows the difference  between higher and
 lower heating value  as a function of MOISTURE and
 HFAC.  For  these  calculations,  all input  streams
 containing  liquid   water . should  b'e.  considered
 fuel/waste  streams;  thus, a  pure water  stream from
 equation 6 would have a  LHV  of  -2,440  kJ/kg  (-
 1,060 Btu/lb).  The  value  of the combustion water
 parameter  is calculated from equation 7: ..
                              35.5 /  2
where H and Cl are the mass fractions of H and Cl in
the  dry  fuel/waste.  Figure B-6  shows that HFAC
increases sharply with H and  decreases slightly with
Cl. The sensible heat input of a stream is the product
of the mass flow of the stream (m), the  mean heat
capacity of the stream,  and the difference between
the preheat temperature  (Tpreheat) and  the reference
temperature. Under most  conditions,  sensible  heat
may be approximated with  reasonable accuracy from
equation 8:
    Sensible Heat Input = 1.01 m(Tpreheat- 298)
                                              (8)
where sensible heat is in units of kJ/kg and Tpreheat
is in °K, and 1.01 kJ/kg is the heat capacity of air.

B.3.2 Example Test Case
This section describes an example application of the
calculation technique discussed above.  The example
test case  is for a rotary  kiln/SCC incineration system
that is  shown  schematically in Figure  B-7.  Control
parameter inputs, which  are summarized in Table B-
2,  were taken from design data  supplied  by  the
applicant for a representative operating point.
       -  '     '      .     «'    '   '        "
The rotary kiln has a volume of 160 m3  (5,650 cu ft),
an  inside surface area of 320 m2 (3,440 sq ft), and a
0.21-m (8.2-in)  thick  refractory  covering  with a
conductivity of 8.2 x  1CH  kJ/s-m-°C  (5.7  Btu
in/hr-sq.ft-°F).  For  the  operating  point of  interest,
the rotary kiln has three  input  streams: waste, steam
used to atomize liquid waste, and air. The feed rates
for  the three streams  are  1.05 kg/s   (8,330 Ib/hr)
waste, 0.096 kg/s (760  Ib/hr), steam,  and 5.39  kg/s
(42,800 Ib/hr) air, including 0.067 kg/s (530 Ib/hr)
water vapor  in the  ajr. The preheat temperature is
450°K (350°F) for the steam, and 289°K (60°F) for
both the waste and the air. The waste stream has an
HHV of 7,690 kJ (3,310  Btu/lb), with 1,24 dry  weight
percent hydrogen, 5.83 dry  weight percent chlorine,
and 18.47 weight percent water.
 Using the  above  data, the  necessary  normalized
 parameters for the rotary kiln may be calculated.  To
 calculate the total heat input, chemical heat from the
 waste stream  must  be considered  along  with the
 sensible  heats of  all  input streams. For this  waste
 composition, the combustion  water parameter  HFAC
 is calculated from equation 7:
     HFAC =
                0.0124
0.0583

 35.5
18
—  = 0.0968
 2
 This  value  of  HFAC,  combined  with  a MOISTURE
 value of 0.1847  and a Cl value of 0.0583, can  be
 used to obtain the LHV of the waste from equation 6:

 LHV  =  7,690 - [(1 - 0.1847) 0.0968 + 0.1847] 2,440
           - 0.0583  (1 - 0.1847) 1,160
      = ,6,990 kJ/kg (3,006 Btu/lb)

 Because the water stream is input in  the vaporized
 form of steam, its LHV is 0. The chemical heat from
 the waste stream (and the total chemical heat in this
 case) is calculated from equation 5:

 Chemical Heat Input  =1,05x6,990
                     = 7,340 kJ/s (25 x 106 Btu/hr)

 The mass  flows  and preheat temperatures of each
 stream may be substituted in equation 8:

 Sensible Heat Input  = 5.39 x 1.01  (289 -  298)
                    = -49 kJ/s (-167,000 Btu/hr)
                      for air,

                    = -9.5 kJ/s (-31,000 Btu/hr)
                      for the waste, and

                    = +14.7 kJ/s (50,000  Btu/lb)
                      for the steam,

amounting to a total sensible heat input of  -43.8 kJ/s
(-150,000 Btu/hr). The total  heat input to the kiln
may be calculated from equation 4:

Total heat input   =  7,340 -  43.8
                 =  7,300 kJ/s (24.9 x  106 Btu/hr)

Because the sum of all feed rates to the kiln is 6.54
kg/s (51,900 Ib/hr),.

Total heat input/total mass input
                     = 7,300 * 6.54
                     = 1.120kJ/kg (480 Btu/lb)

Assuming 10 percent heat loss from the kiln, e.g., the
example test kiln  is very long and, thus," is expected
to have a high heat loss, the ideal  kiln temperature
may be  estimated  to  be 1,200°K  (1,70Q°F)  from
Figure  B-3.  This ideal  temperature  must  be
corrected to take  into account the high  heat capacity
                                                  92

-------
 Figure B-3.  Ideal temperature vs. total heat input to total mass input ratio and fractional heat loss.

      2,500
       2,000
  CD
  ' 3
  ra
  cu
  a
  E
  CD
       1,500
       1,000
                                                                                            - 1,600
                                                                                            - 1,400
                                                                          a>
                                                                          o.

                                                                          0)
                                                                          t-


                                                                    1,200  •§
                                                                                            -  1,000
           300
400             500             600

          Total Heat Input/Total Mass Input (Btu/lb)
                                                                           700
                                                                800
of the water in the combustion  gas.  All three input
streams  contain water: 0.19 kg/s (1540 Ib/hr)  in the
waste, 0.067  kg/s  (530 Ib/hr)  in  the  air,  and  0.096
kg/s (760 Ib/hr) of steam. Thus,  there  is a total of
0.35 kg/s (2,800 Ib/hr)  water input to the kiln, which is
5.4 percent of the total input mass flow. From  Figure
B-4, at  an  ideal  temperature  of  1200°K  (1700°F)
and  5.4 percent  water,  the actual temperature is
predicted to be  34° K (61 °F)  lower  than  the ideal
temperature, or 1,170°K (1,640°F).

The  ideal  residence time may  be estimated from
equation 1:

  ^ideal  =  (353 x 160  x 1)^(5.39 x 1,170) = 9.0 s

This may be  corrected for water  using  Figure B-2.
For mmoisture/mair of 0.35/5.39 = 0.065. The ratio of
the actual to the ideal residence time is 0.88; thus the
estimated  actual residence  time is  7.9  s. The
volumetric flbwrate may be calculated from equation
2:

Volumetric Flow = 160 T 7.9
                 =  20.3 m3/s (43,000 acfm)

To carry but this  analysis  on the SCC, the procedure
is the sajme except that the mass and  energy carried
                            over from the kiln must be considered. The total heat
                            leaving the kiln is the heat entering the kiln minus the
                            10 percent heat loss which is 7,300 - 0.1 x  7,300 =
                            6,570  kJ/s (23.2 x  1fj6 Btu/hr).  However, 0.42 kg/s
                            (3,370  Btu/hr) of ash is removed from  this stream
                            before  it enters the  SCC. From equation 8,  the
                            sensible heat of the ash being removed at 1,170 K is
                            370 kJ/s (1.26  x 106  Btu/hr), so  that the  net  heat
                            going from the kiln into the SCC is  6,200  kJ/s (21.2 x
                            106 Btu/hr).
                           The SCC has a volume of 113 m3 (4,000 cu ft), and
                           an inside surface area of 147 m2 (1,580 sq ft). It has
                           a  refractory  covering  0.21  m  (8.2 in)  thick with a
                           conductivity  of  5.05  x  10"*  kJ/s-m-°C  (3.5  Btu
                           in/hr-sq ft-°F).  In addition to the carryover from  the
                           kiln, for the operating  point of interest, the SCC has
                           four  other  input streams:  waste,  auxiliary  fuel,
                           atomizing steam, and  air.  The feed  rates for these
                           streams  are 0.26 kg/s  (2,060 Ib/hr) waste, 0.062  kg/s
                           (490  Ib/hr) fuel,  0.093 kg/s (738  Ib/hr)  steam,  and
                           3.16 kg/s (25,100 Ib/hr) air  (including 0.04 kg/s [334
                           Ib/hr]  water  vapor  in  the  air).   The  preheat
                           temperatures for all fresh streams are 289 °K (60 °F),
                           except for the  steam, which is preheated to 450 °K
                           (350°F). The waste stream has  a HHV of 23,300
                                                   93

-------
Figure B-4.   Correction to Ideal temperature vs. Ideal temperature and water/total mass flow ratio.

                                                      Ideal Temperature (°K)

                          1000             1200             1400            1600
                                                                                             1800
        500
       400
   0>

   3    300
   Q.


   (D
B    200

 i

£

(0
   Q.

   ID
     100
      -100
                            I
                                          I
                                                                            0%
                                                                                                           200
                                                                                                              0)

                                                                                                              3
                                                                                                           100
                                                                                                              0)
                                                                                                              a

                                                                                                              
-------
 kJ/kg  (10,000  Btu/lb), with  5.86 dry  weight  percent
 hydrogen, 25.70  dry weight percent Cl,  and  no
 moisture. The fuel stream has a HHV of 44,000 kJ/kg
 (19,000  Btu/lb)  with  12.65 dry  weight  percent
 hydrogen, and no moisture.

 Following the  same  method as  for  the  kiln  input
 streams,  HFAC is  calculated as 0.4625 for the waste
 and 1.1388  for  the fuel from equation  7.  From
 equation 6, the LHVs are 21,900 kJ/kg (9,420 Btu/lb)
 for the waste and 41,200 kJ/kg (17,700 Btu/lb) for the
 fuel. From equation  5, the chemical heat inputs are
 5,700  kJ/s (19.5 x 106 Btu/hr) for  waste  and 2,550
 kJ/s (8.7 x  106 Btu/hr) for fuel for a total chemical
 heat input of  8,250  kJ/s  (28.2 x 106 Btu/hr).  From
 equation  8, the sensible heat  of  the fresh  input
 streams is  -2.36  kJ/s  (-8,100  Btu/hr)  for  waste,
 -0.56 kJ/s  (-1,910  Btu/lb)  for  fuel,  +14.28 kJ/s
 (48,800  Btu/lb) for steam, and -28.72 kJ/s (-98,200
 Btu/lb)  for air. Thus, the total sensible heat input,
 including  the carryover from the  kiln,  is 6,180 kJ/s
 (21.1  x 106 Btu/hr).  From equation  4,  the total heat
 input to the SCC is  14,400 kJ/s  (49.2 x 1Q6  Btu/hr).
 The total  mass flow is 9.7 kg/s (77,000 Ib/hr), so the
 total heat/total mass input is 1,480 kJ/kg (640 Btu/lb).

 Because  the SCC is much  shorter than the kiln,  a
 smaller  fractional  heat  loss is  expected.   Thus,
 assuming 5 percent  heat loss,  the  ideal afterburner
 temperature is estimated  to  be  1,520°K  (2,280°F).
 The air,  the steam,  and the kiln  effluent  have  a
 combined 0.48 kg/s (3,800 Ib/hr) water,  which is 4.9
 percent of the total input mass flow. From Figure  B-
 4, the temperature  correction is 50 8K (90 °F), and the
 estimated actual temperature is 1,470°K (2,190°F).

 The ideal residence  time from  equation 1  is 3.2  s
 (using  the combined air flows  to  the kiln and the
 SCC),  and  the ratio of actual-to-ideal  residence
 time is  0.89. Thus,  the  estimated  actual  residence
 time in  the SCC is 2.8 s. The volumetric flow from
 equation 2 is 40.4 m3/s (86,000 acfm).

 Detailed energy and  mass balance  calculations were
 performed for  this  example  using the  computer
 program described in Appendix  E. Results  of the
 calculations and correlations  were compared with the
 design calculations of the permit  applicant in Table
 B-3. The  program, the correlations, and the  design
calculations all showed  excellent agreement  in
calculating temperatures and  flows.  Thus,  it can be
concluded that these correlations  agree quite well
with the energy and mass balance program on which
they are based. It can  also be concluded that this
construction   permit application  is based  on
reasonable design  calculations  and  that the
manufacturer's  claims concerning temperatures and
flows are achievable.

The energy  and  mass  balance  program  is the
preferred  method for performing these  calculations.
 Although  the correlations  have been  shown to be
 viable, to use them can be tedious. Errors can result
 from  calculational mistakes, inaccurate graph
 readings, or poor assumptions (such as the assumed
 heat loss from each combustion chamber).


 B.4 Air  Pollution Control Equipment
 Th3  two  kinds  of pollutants  that  emerge  from
 hazardous waste incinerators are gaseous  pollutants
 and particulate pollutants. Because hazardous wastes
 are  often highly  chlorinated, the gaseous pollutant of
 greatest concern is HCI.  Flyash comprises most of
 the  particulate pollutants.  Flyash particles  emerging
 from incinerators typically have mass mean diameters
 of >10 urn.  However,  they have broad distributions;
 thus, there may be a significant fraction of particles in
 the submicron range. In addition, high concentrations
 of toxic heavy metals tend  to "be found  in submicron
 particles.  Therefore, APCE for  incinerators burning
 metal-containing  wastes  should effectively  remove
 small particles.

 Hazardous  waste  incineration  systems  generally
 employ more than one type of pollution control device
 to remove both  particles and gases effectively.  The
 APCE must  be  properly  designed, operated,  and
 maintained  to  achieve  design  performance
 continuously  under  a variety of incinerator operating
 conditions. The permit  writer must,  therefore, review
 the proposed APCE design as presented in the permit
 application.  It should be assessed  for engineering
 soundness, and an estimate should be made whether
 the APCE can achieve the performance expected in
 the trial burn. Calculations should be made to verify
 many of  the  system and  operating parameters to
 ensure their consistency and soundness.

 Specifically,  the  APCE  specifications should be
 reviewed to ensure the following:

 • Sufficient quench water is available to cool the  flue
  gas  to the  recommended APCE operating
  temperature.

 • Sufficient fan  capacity is available to handle  the
  maximum expected gas flowrate.

 • The system can meet the 180 mg/dscm particulate
  performance standard  for  the  expected  particle
  loading and size distribution.

 • The system can  meet  the 99 percent Cl  removal
  performance standard  for the  expected  total Cl
  feed rate.

This section will  present a  brief description  of most
types of APCE and provide the  permit writer  with
several  tools to  help verify expected  system  and
operating parameters and performance.
                                                 95

-------
co
05
Table B-2. Input Data for Energy and Mass Balance Example

Primary waste
Primary fuel
Secondary waste
Secondary fuel
Primary air
Secondary air
Secondary water
Primary water
Ash dropout
Proximate analysis
(as received) (percent) Heating Elemental analysis (dry percent)
Feed (higher)
rate Preheat Fixed asrecvd)
(Ib/h) (°F) carbon Volatiles Ash Moisture (Btu/lb) C H N S Ash O
8,330 60 4.42 23.12 53.99 18.47 3310 22.85 1.24 0.0 3.86 66.23 0.0
Q 	 	 	 	 	 	 	 . 	 	 	 	 	
2,060 60 0.0 100.0 0.0 0.0 10,000 55.18 5.87 0.0 1.86 0.0 11.39
490 60 0.0 100.0 0.0 0.0 19,000 87.35 12.65 0.0 0.0 0.0 0.0
42,800 60
25,100 60
738 350
760 350
3,370
Design Specifications Primary Secondary
Refractory thickness (in) 8.2 8.2
Refractory conductivity [(Btu)(in)/(h)(ft2)(°F)] 5.7 3.5
Unit volume (ft3) 5,650 4,000
Refractory surface area (ft2) 3,440 1,580
Cooled surface area (fi2) 0 0

Cl
5.83
—
25.71
0.0








-------
         B.4.1 Wet Systems
         Wet  APCE  is  predominant  among  existing
         incinerators. Typical equipment that is used includes
         quench chambers, scrubbers, and wet  ESPs. Most
         systems are designed for particulate  control.  The
         capture of  HCI also occurs because of the solubility
         of the acid in water.  The control efficiency  for HCI
         can be enhanced by adding a caustic solution to the
         scrubbing water. Caustics such as NaOH or NaCOs
         are also used to control the pH of water recirculated
         to the wet scrubber. Control of pH requires 1.10 kg of
         NaOH or 1.46 kg of CaCOa per kg HCI. Figure B-8
         presents a  layout of a typical wet control system.

         Quench Chambers
         The  quencher  often  precedes  the  scrubber
         equipment. Its function is to reduce the temperature
         of the hot gases leaving the thermal equipment units
         and  to increase the  humidity of the gases  to the
         saturation  point.  This action  reduces  water
         evaporation in the downstream scrubbing equipment
         and alleviates the potential problems associated  with
         particle generation in  caustic scrubbers. Also,  the
         quencher facilitates particulate scrubbing by initiating
         particulate  agglomeration as  well as protecting the
         downstream  equipment from  high-temperature
         damage. Because particulate scrubbing occurs in the
         quencher,   these units  are also called  spray
         scrubbers.  Designed  as  integral  parts  of  a  venturi
         scrubber, some quenchers are located at the inlet  of
         the scrubber converging section.

         A  constant  gas temperature at the quencher outlet
         often  signifies proper  operation  of  the  unit. This
         temperature  is typically maintained  close  to  the
         saturation temperature of the gas, 82 to 93°C (180  to
         200°F). Often, the quench water is recirculated from
         the sump back to the inlet to minimize water  use.
         However, even in closed loop  systems, some amount
         of water makeup  is required  to replace the  amount
         lost through  evaporation. Optimum  operation would
         use only makeup water (about 50 to 80 percent  of
         evaporative  loss)  to  minimize  reentrainment  of
         particulate  back into  the  gas  stream. Quench water
         requirements to achieve  saturation temperature  can
    Table 8-3.   Comparison of EER Energy and Mass Balance
              Results with  Permit Application Design
              Calculations

Rotary kiln temp. (°F)
Flow (acfm)
SCO temp. (°F)
Flow (acfm)
EER Energy and
Mass Balance
Program Correlations
1,623. 1,640
41,821 43,000
2,218 2,190
85,742 86,000
Permit
Application
Design
Calculations
1,600
41,922
2,200
84,668
    be calculated as follows:
                        18
                    MW.
                       DG
(p-Vo)
                                     KG)
                        (9)
   where:
      MW    = Quench  water  feed  rate  which  yields
               saturation (Ib/hr).

      PH2O   = Vapor pressure of  moisture   (psia)
               (function  of inlet gas temperature).
             = DrV 9as molecular weight.

             = Absolute pressure (psia).
      MQ    = Dry gas mass flowrate (Ib/hr).

   Up to this quench feed water rate, both sensible and
   evaporate cooling occur.  Any additional quench feed
   water cools through sensible heat transfer. Generally,
   for quench/venturi  scrubber applications, only  80
   percent  of the  evaporate water  less  (FW) is
   recommended for  the  quench chamber  with a gas
   temperature slightly above  saturation (e.g.,  93°C
   [200° F]). The total water  vapor mass flowrate leaving
   the quench is:
         Figure B-7.   Schematic of incinerator for energy and mass balance example.
                                                              Waste  Fuel  Steam  Air

                                                                11     11
            Waste


            Steam


             Air
1
k
k
f
Kiln



^
r
Afterburner

L
f
                                                     Ash
k
97

-------
 Figure B-8.  Typical APCE schematic (wet system).
                                                                                              Process water
  Hot
  untreated
  gas
          TIC -Temperature indicator controller
          LIC - Level indicator controller
          FIC - Flow indicator controller
          PI   - Pressure indicator
          Fl   - Flow Indicator
          AIC - Analysis (pH) indicator controller
          Al   - Analysis (Oz, FO, COz) indicator
                                                                               To permitted landfill
                                                                               or waste pond
            FH.O(out) = MW + FH Q(in)
(10)
where:
            =  Mass  flowrate  of  water  vapor  in
               entering gas, (Ib/hr).
A regimented maintenance program for the quencher
should  be followed to ensure  that effective water
spray (unobstructed nozzles) is retained.

Several types of wet scrubbers  are used in industry.
Despite their low mechanical efficiency, the adjustable
and fixed throat venturi scrubbers are most commonly
used for incinerator applications  because of their high
particulate  collection efficiency.  Other  scrubber
devices include packed bed (vertical and horizontal),
tray or plate, impingement, entrainment, mechanically
aided, and ionized  scrubbers. They remove gaseous
pollutants through the  mechanism  of  absorption.
Alkaline scrubbing solutions  are  often  used  to
increase the rate of mass transfer and to  neutralize
acids.

Packed-Bed  Scrubbers
Absorption   removal  efficiency  for packed-bed
scrubbers can be described  by the number of transfer
units attained by a device. Efficiency increases with
increasing  number of transfer units. The number of
transfer units can be found from:
                          NTU = Z^-HTU              (11)
         where:
                 = Number of transfer units
                 = Scrubber length (m)
                 = Height of a transfer unit (m)
         The  number of transfer units  increases,  and, thus,
         efficiency  increases  with increasing scrubber  length.
         The height of a transfer unit is generally determined
         empirically for  different packed-tower configurations.
         The  height  of  a transfer  unit  generally decreases,
         and,  thus, efficiency increases with increasing L/G
         ratio, packing interfacial area, and gas diffusivity.

         Venturi Scrubbers
         Venturi scrubbers  atomize water into small droplets
         and  then  use  the  droplets  to  collect  particles.
         Efficiency  generally  increases  with  increasing L/G
         ratio,  throat velocity,  and  particle size.  Particle
                                                   98

-------
collection efficiency in a  venturi scrubber  can  be
estimated using the equation of Calvert (1972) (7):
    Efficiency = 1 - exp[(QL/QG) x UG x F(Kp)]
where:

   CL-
   OG
   UG
   Kp
                                             (12)
= Liquid flowrate (m3/s)
= Gas flow velocity (m3/s)
= Gas throat velocity (m/s)
= Inertial impaction  parameter (a function of
  particle size)
This  equation  and Figure 2-3  show  that  scrubber
efficiency is a  function of the pressure  drop across
the  venturi,  which can  be  estimated  using  the
following empirical equation (8):
                          .0.133.0.78
                               L
                 AP=-
                          1,270
where:

   AP
   VT
   PG
   AT
   L
                                              (13)
= Pressure drop in
= Throat velocity (fps)
= Gas density (Ib/cu ft)
= Area of throat  (sq ft)
= L/G ratio (gal/1,000 cfm)
For a fixed gas flowrate and throat area, control of AP
inherently controls the amount of  liquid or  L/G  ratio
required. Typically, the higher the AP, the greater the
efficiency.  Some scrubbers at  existing incinerators
operate with AP as high as 2.0  m H^O (80 in W.C.)
or higher.  Venturi  scrubber  operation  is  optimum
when the AP is  maintained relatively constant  (<5
percent variation  in AP), which  can be achieved by
proper setting  of the liquid flow and adjustment of the
throat when allowable..  Routine  maintenance  of the
nozzles and visual inspection of  the critical parts of  a
scrubber (e.g., throat) are important for the equipment
to maintain design performance.

Scrubbers  in  general can also be  used  for  acid
emission control  by  adding caustic  solution  to the
spray water. Although venturi scrubbers can be  used
to absorb HCI, the most commonly used  absorbers
are  the  packed,  tray,  or   spray  towers.  Good
absorption  efficiency  is  primarily a function  of L/G
distribution, alkaline concentration  of  scrubbing
solution, gas,  water temperature, and  gas residence
time  (face velocity). For packed-bed scrubbers, the
packing depth  (Z) is defined as follows (3):
where the constant 4.6 is determined by the  natural
logarithm of the scrubbing efficiency (e.g., In 100/1
for 99 percent efficiency), ACFS is the actual cu ft/s
of the flue gas, P is the total pressure, and Kga is the
absorbing  capacity  of  the scrubbing solution  as
shown  in Table B-4. From these data, it is  evident
that when excessive C\2  is  anticipated,  a  caustic
solution is necessary to absorb  the  free chlorine,
whereas HCI can  effectively be scrubbed  with water
because of its high solubility.

Table B-4.   Typical Values of Kga  (B-3)
Gas
CI2
HCI
SO2
SO2
CI2
Scrubbing Kga,
Solution (lb/mole)/(in-H2O-cu ft-sec)
NaOH
H2O
NaOH
H20
H2O
1.4 x 10-5
1.1 X TO'5
4.8 x 10-6
2.2 x 10'7
9.5 x 10-8
The packing material and tray and plate arrangement
also provide the mechanism  for particulate collection
utilizing the hydraulic energy of the liquid and mass
transfer of the solids from the gas into  the scrubbing
liquid. As in the quencher and  venturi,  the scrubbing
water or liquor is recirculated.  This process  requires
careful monitoring of the solids and pH level of the
scrubbing  solution to  maintain equipment  design
performance.  Relatively constant pressure  drop
across  these  units  is  also   indicative of  good
operation.  Because localized plugging  may occur in
these units, routine maintenance and  inspection are
necessary.

All  scrubbers  are equipped  with  separators  or
demisters. These  are  passive  units  which  are
designed to trap water droplets  entrained with the flue
gas prior to the stack.  Although important for system
design evaluation, this  equipment requires little or,no
consideration in the operating permit once its design
has  demonstrated compliance  with the particulate
emission standard.

Additional wet  particulate  control  devices  are
electrically-induced systems  such  as the IWSs  and
wet  ESPs. These units compensate  for the  lower
kinetic energy of high-pressure-drop  systems by
ionizing the gas stream. Performance of these units is
strictly a function of secondary voltage  and electrical
current, gas  flowrate,  and scrubber  water flowrate.
Ionized wet  scrubbers  combine  the  principle  of
electrostatic  particle  charging  with  packed-bed
scrubbing  technology.  A  constant DC voltage is
applied in the  ionizing  section.  Because wetted
positively charged plates  are continuously flushed, the
buildup of a resistive layer is  prevented. The flue gas
leaving the ionizing section is  further  scrubbed in  a
packed-bed.  The  efficiency of  IWSs  is relatively
insensitive to  particulate resistivity,  but control of
constant voltage and  packed-bed  scrubbing  water
flowrate is required.
                                                  99

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 B.4.2 Dry Systems
 The most  commonly used  dry  participate collection
 systems are mechanical collectors,  ESPs, and  FFs.
 Although these alternative  control devices  are
 currently  less  popular  than  their counterpart  wet
 systems  for  complete  emission  control, these
 alternative  control devices  may  be  the systems of
 choice  for future  incinerator  facilities  because  they
 require  reduced  residue  handling  and disposal
 requirements.  Several  of  these technologies  are
 currently used in combination with wet technologies.

 Mechanical Collectors
 Mechanical  collectors remove particles  through  the
 forces of inertia and gravity. Cyclones are the most
 common type of mechanical collectors. In a cyclone,
 the air flow impinges tangentially onto the inner wall
 of a cylinder.  Particles strike the cylinder wall and
 then slide down  into  a  hopper, where they  are
 removed. The  most important operating  parameters
 are particle size, gas  flowrate,  and  cyclone  design
 geometry. Cyclone efficiency can be estimated using
 the equation of Lapple (1951) (9):
             Efficiency .=
                                       (14)
where:

   K
   V
   V
   p
   dp
                         1+ K /V  AT
                               ^  P/  P
= Cyclone geometry factor (m)
= Gas viscosity (kg/m-s)
= Inlet gas velocity (m/s)
= Particle density (kg/m3)
= Particle diameter (m)
Cyclones are  not highly efficient  (e.g.,  <90  percent
control),  but they are inexpensive,  and, thus, are
often used as methods of pretreatment before other
APCE.

Electrostatic Precipltators
Electrostatic  precipitators  remove  particles  by
charging them and then collecting them on oppositely
charged  plates.  Plates are  periodically rapped to
remove the collected particles.  The ESPs are highly
efficient,  even for submicron particles. For example,
typical ESP efficiency might exceed 99 percent for 5
mm  particles,  dip to 95 percent for  1  mm particles,
and  again increase  to  above 99 percent for 0.1 mm
particles.  Submicron particle collection  efficiency  is
high  because  the mechanism of Brownian diffusion
increases the ability of  submicron  particles to  migrate
to collection plates. Collection efficiency increases
with  increasing plate area  and applied voltage and
decreases  with  increasing  gas  flowrate.  ESP
efficiency  can be   predicted  using the  Deutsch
equation:
                                                           Efficiency
                                               where:)
                      = 1 — exp(
-AW\

~Q~J
(15)
   A   = Plate area (m2)
   W  = Particle drift velocity (m/s)  (a Junction of
         applied voltage and particle size)
   Q   = Gas flowrate (m3/s)

 Dry ESPs  are much  more efficient in capturing small
 size particles (<10 pm)  than cyclones.  Contrary to
 wet ESPs, however, the collection efficiency is also a
 function of particle resistivity,  which, in  turn, will vary
 with waste type burned as well  as gas temperature
 and acid concentration in the flue gas.

 Fabric Filters
 Filters remove particles by collecting  them on filter
 fibers  or on  previously  collected  particles. The most
 commonly  used types are fabric filters (FFs), in which
 gas flows through  parallel  arrangements of filter bags.
 Bags are periodically  cleaned by shaking or reversing
 the air flow.  Well-maintained  baghbuses  are highly
 efficient, but  problems  may arise if the gas stream
 has high moisture or acid content or if holes or cracks
 develop in the  bags from manufacturing flaws  or
 aging.

 Efficiency  increases  with  increasing  pressure drop
 and decreases with increasing  air-to-cloth ratio.
 Fabric  filters  often have  collection  efficiencies in
 excess of 99 percent, exclusive  of water  vapor and
 condensibles. The type  of material used for the bags
 varies with  such factors  as temperature,  humidity, and
 chemical  characteristics  of  the dust  and  gases.
 Maximum gas temperature inlet is typically 260 °C
 (500 °F), although  it varies according to the  type of
 material. Steady pressure drop  across  the  FF is
 indicative  of  good  operation  with the  minimum AP
 defined by  the manufacturer for operation  with clean
 bags.  Careful temperature .control is  necessary  to
 minimize water  vapor  condensation,  blinding, and
 corrosion.

 Spray Drying Absorbers
Acid  absorption can  also be  achieved in the gas
 phase using  spray drying absorbers (SDAs). In this
 process, a solution,  slurry, or paste  containing an
absorbent is atomized and injected into the flue gas.
The amount of water injected is not sufficient to lower
the temperature  to  the  dew point, and  the atomized
 material is  transformed  into  a  dry,  free-flowing
product. The  chemical reaction between HCI and the
caustic absorbent occurs in the gas phasa-in contrast
to wet scrubbing devices.  Thus, particulate control is
necessary downstream of the dry  scrubber to prevent
the escape of the caustic and salts to the stack.
                                                 100

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 B.5 Measurement Techniques and Safety
 Interlocks
 The measurement techniques should be reviewed to
 verify that appropriate QA/QC requirements are met
 as  described  in  Reference  10.  Special  attention
 should  be  paid  to  critical  measurements  such  as
 temperature and gas concentrations.

 Thermocouple placements should be so marked that
 the  temperatures that  are being measured  and
 reported are clearly  indicated. Each  thermocouple
 should  be  described in  the application as to type,
 sheath  or  shielding  material,  sheath  or shielding
 diameter, the proximity and  visibility of any flames or
 cooled  surfaces,  and. the  typical  condition  of the
 thermocouple during  operation,  e.g.,   clean,
 blackened,  or  slagged. This information is important
 because the temperature a thermocouple measures is
 not truly the gas, temperature but is an equilibrium
 temperature based on radiative and convective heat
 transfer between   the  thermocouple and  its
 surroundings. When radiative  heat  transfer  is
 significant, the thermocouple reading may be too high
 because radiative  heat,is transferred from the flame,
 or it may  be too  low because the radiative heat is
 transferred  to  cooled  surfaces or incinerator walls.
 Radiation  becomes  more significant  for high
 temperatures, large thermocouple sheaths, blackened
 thermocouple sheaths, and increased visibility of the
 flame or cooled surfaces. If  these conditions change
 drastically  from those of the trial  burn because  of
 change  in operation, thermocouple deterioration,  or
 thermocouple, replacement,  the permit  limit
 temperature as measured by the thermocouple during
 the trial  burn may no longer be the conservative level.

Thermocouple placement   is discussed  in  the
 Engineering  Handbook for  Hazardous  Waste
 Incineration  (SW-889),  Briefly, the thermocouple
 must be placed in the center of a turbulent zone  of
 the gas  stream exiting the combustion chamber. It is
 typically placed as close to the center of the gas flow
 as possible.  Shielding must be provided to prevent
 direct impingement of radiation from the flame and
 from  glowing portions of the  wall  onto  the
thermocouple housing.

 Gas concentration measurements can be made on a
 wet or on a dry basis. Concentrations measured on a
 wet basis can be substantially lower  than  those
 measured  on  a dry  basis, especially  if the
measurements are taken from the stack  gas, which is
typically saturated with  water.  The  permit  writer
 should  be  aware of the   basis  on   which gas
concentrations  are reported and should  take this into
account in any calculations such as the energy and
 mass  balance  calculations  described elsewhere   in
these appendices.
Automatic waste feed cutoff  is required when  permit
limits for group  A and  group  B parameters are
exceeded.  The  permit writer  should examine the
schematic  diagrams  for the  instrumentation  and
control systems to verify that the  safety interlocks for
waste  feed  cutoff  are  tied  to  the appropriate
monitoring devices.


B.6 Special Wastes and Similar Systems
The guidelines for evaluating incinerator  design and
setting permit limits outlined in this handbook are not
universally  applicable. For example, a waste with a
high content of  toxic metals may warrant special
consideration.  Some  toxic metals  may vaporize in
high-temperature incinerators and condense on the
surface  of  fine  particles. If  the  waste has a high
concentration of  toxic metals, the permit writer may
want to  set a maximum and  a minimum  combustion
chamber temperature  limit and may want  the  trial
burn to  meet  fine  particulate  as  well  as  total
particulate emissions standards. Specific guidance on
toxic metals from incinerators will be  developed  by
the EPA (see Appendix A).

In  evaluating incinerator designs, the permit  writer
should take into account the design and performance
of  similar incinerator systems.  Such  design >and
performance data  may be accessed through  the
HWCTDB that is  maintained at the ORNL.


B.7 References
1.  Vogel, G.A.,  et al. Incinerator and Cement Kiln
    Capacity for  Hazardous Waste  Treatment.  EPA-
    600/2-86/093  (NTIS PB87-11089C/AS).  1987.

2.  Kiang, Y.H. and A.A. Metry.  Hazardous Waste
    Processing Technology. .Ann  Arbor,  Michigan:
    Ann Arbor Science Publishers. 1982.

3.  Bonner,  T.A. Engineering  Handbook  for
    Hazardous  Waste Incineration.  EPA-SW-889
    (NTIS PB81-248163).  1981.

4.  Seeker, W.R., W.D. Clark, and G.S. Samuelsen.
    The  Influence of Scale and Fuel Properties on
    Fuel Oil Atomizer Properties.  Presented  at: The
    Joint EPA/EPRI   Symposium  on Stationary
    Combustion NOX Control, Dallas, Texas. 1982.

5.  U.S.  Bureau  of Mines. Technical Paper  384.
    1927.

6.  Li, K.W. Applications of Khodorov's and Li's
    Entrapment Equations to Rotary Coke Calciners.
   AlChEJ. 20:1017. 1974.
                                               101

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7.  Calvert,  S., D. Goldschmid, and  D. Mehta.    10. Midwest Research Institute.  Hazardous Waste
   Scrubber  Handbook.  U.S. Department  of       Incineration  Measurement  Guidance Manual.
   Commerce. NTIS PB-213016. 1972.                 Prepared for U.S. Environmental Protection


                                                          3-
9.  Lapple,  C.E.  Processes Use Many  Collector
   Types. Chemical Engineering.  58:144. 1951.
                                           102

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                                           APPENDIX C
                Time and Temperature Dependency of the Destruction Process
Incineration  is a high-temperature oxidation reaction
process  governed  by chemical reaction  equilibrium
and kinetics. The basic reaction equilibrium parameter
is the equilibrium constant  at  constant pressure
expressed mathematically as follows:
                                              (1)
where,

   Kp(T)  = exp(-AE/RT)

Where Ppj  and Prj  are the  partial  pressures of
products  and reactants, respectively, and ai and pi
are the chemical reaction constants. The equilibrium
constant  Kp is an exponential function of temperature
(T) and free energy (E) of each reaction component.
In  all practical  combustion  systems,  the  chemical
reaction  involves  several  intermediate  reaction
products  that exist  for a limited amount of time. This
time dependency  is  taken into  consideration  by
chemical  reaction  kinetics  and  is expressed  as
follows:
                                              (2)
where A and E are the organic compound Arrhenius
rate constants  (determined  empirically  using
laboratory thermal decomposition devices), R  is the
universal gas constant, T and Ax are temperature and
time available at that temperature, CA and CQ are the
concentrations of the compound at time T, and t = 0,
respectively.

These  expressions indicate that temperature  is the
primary  parameter in  driving  reactions  to equilibrium
and the predominant force of the reaction rate for all
chemical  compounds. High  temperature  is also
necessary to provide  the thermal  energy to heat,
vaporize, and devolatize organic compounds trapped
in  the  waste  feed.  Heating, vaporization, and
devolatilization  are  necessary  first  steps  for
combustion of fuels and destruction and oxidation of
all  toxic  organic compounds. Thus, temperature in
each  thermal chamber  is  the  primary  control
parameter  needed  to ensure  high  destruction
efficiency  (DE) of organics in  hazardous waste
incinerators. The  temperature  in  each chamber
should be controlled to the demonstrated minimum.

The kinetic rate expression suggests that for organics
fed in the PCC, the DE (1  - CA/CQ) is the result of a
series  of  decomposition reactions  in the PCC and
downstream combustion chambers as illustrated  by
the following expression:
                   C.

                  c~
                   i-i
                            1=1

                                            (3)
where Cn is the concentration of the compound at the
exit of the n
-------
This equation  can be  used to make approximate    estimate of 2.6 x 10'6 s~1  can  be used  for  this
estimates of  gas  phase  decomposition  of  the    purpose if a better value is not available.
compound under well-mixed conditions. An empirical
                                               104

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                                           APPENDIX D
                    Designating Principal Organic Hazardous Constituents

                               Barry Dellinger and Phillip H. Taylor
                             University of Dayton Research Institute
                                           Dayton, Ohio
                         (Duplicated in this document without change)
D.1  Background

The  destruction efficiency  (DE)  of POHCs  is
dominated  by  the temperature,  time,  and fuel/air
stoichiometry (excess air) experienced by the POHCs
in the high temperature  zones of  incinerators.
Calculations and experimental observations  have
shown that  the  emissions of undestroyed,  residual
POHCs  are  kinetically  (reaction  rate),  not
thermodynamically controlled  [Tsang  and Shaub
(1982), Trenholm, et  al (1984)]. Thus, determination
of the exact time, temperature,  and  stoichiometry
history of all the  molecules in an  incinerator  is
necessary to determine the absolute DE of a POHC.
This  type  of information is,  of  course, not  currently
available. However, sufficient information is  available
to estimate the relative DE of potential POHCs.

Simple conceptual and more complex models suggest
that the gas-phase residence  time  and temperature
in the  post-flame or  thermal  zones  of incinerators
control the  relative  emissions  of  most  POHCs
[Dellinger, et al (1986), Clark,  et al (1984)]. The basic
reason behind this is  that all  molecules entering the
flame zone of an incinerator are essentially destroyed
and only the small fraction escaping the flame zone
may  be emitted from  the facility. Various flame zone
"failure modes"  exist  which  may cause  residual
POHCs to be emitted. Once in the  post-flame zone,
gas-phase thermal decomposition  kinetics  control
the rate of POHC destruction and PIC formation and
destruction.

If all POHCs in  a given waste stream in a given
incinerator are volatilized at  nearly the same rate,
they  will  experience the  same  post-flame  gas-
phase residence time, temperature, and stoichiometry
history. This means  that the  gas-phase thermal
stability of  the  POHCs  (as  determined  under  a
standardized set  of  conditions)  may be  used  to
predict their relative incinerability. The temperature for
99%  destruction at  2.0  seconds  gas-phase
residence  time,  [T9g(2)(°C)],  is  one  method  of
ranking the  thermal  stability  of  POHCs. Other
residence times or temperatures  may  be  used  to
develop  this  ranking.  However,  laboratory data
indicate  that  although  absolute  POHC DEs are
dependent  upon time  and temperature,  the relative
DEs,  i.e.,  incinerability  ranking,  are  relatively
insensitive  to these parameters  [Dellinger,  et  ..al
(1984), Graham, et al  (1986),  Taylor and Dellinger
(1988)]. On the other  hand, stoichiometry has been
shown to be  a major variable in determining relative
stability [Graham, et al (1986)  Taylor and Dellinger
(1988)].

Theoretical considerations suggest  that oxygen-
starved  pathways  through the  incinerator  are
responsible for most POHC and PIC emissions. Even
though the  facility may be operating under nominally
excess air  conditions, poor  mixing  will result  in
oxygen-deficient  pockets where the rate of POHC
destruction  is low and  PIC formation  is favored.
Consequently, it is believed that gas-phase  thermal
stability under sub-stoichiometric oxygen  conditions
is an effective  predictor  of  POHC  relative
incinerability.

A recent study compared the incinerability predictions
of several  proposed  POHC ranking methods with
results of  10  pilot-  or  full-scale   test  burns
[Dellinger,  et al  (1986)].  The  ranking methods
included   heat  of  combustion,  autoignition
temperature, ignition delay time, flame failure modes,
theoretical flame mode kinetics, thermal stability  of
pure compounds under excess air conditions, thermal
stability of  mixtures under  oxidative conditions,  and
the thermal  stability  of  mixtures  under oxygen-
starved conditions. Correlations  of the prediction  of
the rankings with  field results  were poor  except  for
thermal stability of  mixtures under oxygen-starved
conditions. Although the laboratory data base used  to
predict full-scale  POHC  DREs was very  limited,
statistically  significant correlations in 7 of 10 cases
                                               105

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were  observed  using  this ranking approach. The
results of  this comparison along  with  theoretical
considerations  suggest that this type  of  thermal
stability  ranking  should  be  used  to replace  the
previously recommended heat of combustion index.


D.2 Construction of the Ranking
Tables 
-------
        the least stable POHC for which 99.99% ORE can be
        demonstrated.

        Another alternative approach involves the use of the
        incinerability class divisions. In this approach, one can
        demonstrate  99.99%  ORE  of  a  group of
        experimentally  evaluated  POHCs  within  an
        incinerability class and  receive approval  to  burn all
        other  POHCs  within  and below that  class.  For
        example,  if  99.99%  ORE can  be demonstrated for
        chloromethane, acetonitrile, and chlorobenzene, the
        facility would be  allowed to burn any  Appendix VIII
        compound. As a second example, if 99.99% ORE is
        demonstrated  for hexachlorobutadiene, methyl ethyl
        ketone, and cresol, the facility would only be allowed
        to burn compounds ranked in class 3 or lower. Since
        the ranking  is subject  to semi-annual  revision,  it  is
        suggested that the ranking which is current when the
        trial burn  is  approved be used  throughout the permit
        process  unless a change  in  POHC selection  is
        mutually  agreed upon  by all  interested  parties.  A
        summary  of the ranking by classes is given in Table
        D-3.

        It should be noted that reformation of a POHC from
        its own decomposition  products or formation of the
        POHC as a  PIC from another waste feed  component
        is  generally  not included as a  factor in this ranking.
        Significantly, laboratory  studies  have shown that  both
        POHC reformation and  PIC  formation  can affect
        observed DEs  [Taylor and Dellinger (1988), Dellinger,
        et al  (1988)].  In some  instances, it  is felt that the
        laboratory  determination  of  Tgg(2)(°C) were
        unavoidably  affected  by  POHC reformation, (e.g.,
        formation of chloromethane from chlorine atom attack
        on  methane). When it was  judged  that  POHC
        reformation was inevitable from almost any waste,
        reformation  was included in  the  thermal stability
        ranking. However, some deviation from  the predicted
        ranking may be expected due  to PIC formation. As
        additional  studies concerning PICs  are completed,
        guidelines for evaluating the role of PIC  formation will
        be furnished.

        The extensive testing conducted by UDRI  has shown
        that  the  ranking of most of  the  compounds is
        relatively insensitive  to  composition of  the  waste
        mixture.  However,  a few  notable  exceptions have
        been  observed  in initial tests.  This includes aniline
        derivatives and PNAs in general. Somewhat lesser
        variability  has been observed for benzene, toluene,
        and pyridine, which  were judged to be  sufficiently
        constant  to be included as experimentally evaluated
        compounds.  Consequently, it  is  suggested  that the
        waste  composition be  carefully  considered  before
        these  compounds are selected  as POHCs. Benzene,
        toluene, and PNAs are expected to be  particularly
        prone to  formation as PICs in full-scale incinerations
        and observed  DREs  may be  significantly affected.
        Effects of PIC formation may be minimized by feeding
        the POHC at a sufficiently high concentration.
Finally, it should be noted that no rankings are given
for PCBs which are listed as N.O.S. in Appendix VIII.
An estimate of  the  stability  of individual  PCB
congeners may  be made  by assuming that the
congener  is slightly less stable than  the  chlorinated
benzene corresponding to the least chlorinated ring in
the  PCB  congener of  interest.  This means, for
example, that dichlorobenzene would  be  a suitable
incineration   surrogate  for   2,2',3,3',4-
pentachlorobiphenyl, monochlorobenzene would  be  a
suitable  incineration  surrogate   for  3,3',4,5-
tetrachlorobiphenyl and pentachlorobenzene would be
a  surrogate  for  decachlorobiphenyl.  As  suitable
experimental data is generated, thermal stability data
on PCBs will be furnished in the updated ranking.

Although  not currently  listed  specifically on  the
Appendix  VIII list,  the incinerability  of chlorinated
dibenzo-p-dioxin  and dibenzofuran isomers  are of
intense interest. As further testing  proceeds, we plan
to  furnish  stability  data  on  these  important
compounds.


D.4 References
 1.  W. Tsang and W. Shaub.  Chemical Process in
    the  Incineration  of  Hazardous Materials,
    Detoxification of Hazardous Waste. J. Exner,  Ed.
    Ann Arbor. 1982, pp. 41-59.

2.  A.  Trenholm,  P. Gorman, and  G. Jungelaus.
    Performance  Evaluation  of  Full-Scale
    Incineration.  MRI Report  Under  EPA  Contract
    68-02-3177.  1984.

3.  B. Dellinger, W. Rubey,  D. Hall, and J. Graham.
    Hazardous Waste  and  Hazardous Materials, 3,
    No. 2, 1986, pp. 139-150.

4.  W. Clark,  M. Heap, W.  Richter, and W. Seeker,
    The  Prediction  of Liquid Injection Hazardous
    Waste  Incinerator  Performance.  ASME  AlChE
    22nd National Heat Transfer Conference. 1984.

5.  B. Dellinger,  J.  Torres, W.  Rubey, D.  Hall, J.
    Graham, and R. Carnes. Hazardous Waste and
    Hazardous Materials, 1,  No.  2. 1984.  pp.  137-
    157.

6.  J. Graham, D.  Hall, and B.  Dellinger. Environ. Sci.
    Technol. 20, No. 7. 1986,  pp. 703-710.

7.  B.  Dellinger,   M.  Graham,  and D.  Tirey.
    Hazardous Waste  and Hazardous Materials, 3,
    No. 3,  1986. pp. 293-307.

8.  P.H.   Taylor  and  B.  Dellinger.  Thermal
    Degradation  Characteristics of Chloromethane
    Mixtures. Environ. Sci. Technol., Vol. 22,. No. 4,
    p. 438. 1988.
k
                                                        107

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 9. P.M.  Taylor  and  J.F.  Chadbourne.  Sulfur
   Hexafluoride as  a Surrogate  for  Monitoring
   Hazardous  Waste Incinerator Performance.
   Journal of the Air Pollution Control Association,
   Vol. 37, No.  6. p. 729.  1987.

10. B. Dellinger, D.A.  Tirey, P.M. Taylor, J. Pan, and
   C.C.  Lee. Products of Incomplete Combustion
   from  the  High  Temperature Pyrolysis  of
   Chlorinated Methanes. 3rd Chemical Congress of
   North America and the 195th National  Meeting of
   the American Chemical  Society,  Division  of
   Environmental  Chemistry  Preprints, Vol. 28, No.
   1. p. 81. Toronto, Ontario,  Canada. 1988.
                                               108
I

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Table D-1.  Principal Hazardous Organic Constituent Thermal Stability Index

 Principal Hazardous Organic Constituent	Rank

 CLASS 1
 CYANOGEN (ETHANEDINITRILE)                                             1
 HYDROGEN CYANIDE {HYDROCYANIC ACID} [2]                                2
 BENZENE [2]                                                            3
 SULFUR HEXAFLUORIDE [3]                                                 4
 NAPHTHALENE [2]                                                        5
 FLUORANTHENE{BENZO[j,k]FLUORENE}                                       6
 BENZO[j]FLUORANTHENE {7,8-BENZOFLUORANTHENE}                           7
 BENZO[b]FLUORANTHENE {2,3-BENZOFLUORANTHENE}                           8
 BENZANTHRACENE (1,2-) (BENZ[a]ANTHRACENE}                                9
 CHRYSENE {1,2-BENZPHENANTHRENE}                                       10
 BENZO[a]PYRENE {1,2-BENZOPYRENE}                                        11
 DIBENZ[a,h]ANTHRACENE {1,2,5,6-DIBENZANTHRACENE}                          12
 INDENO(1,2,3-cd)PYRENE {1,10-(1,2-PHENYLENE)PYRENE}                          13
 DIBENZO[a,hJPYRENE {1,2,5,6-DIBENZOPYRENE}                                 14
 DIBENZO[a,i]PYRENE{1,2,7,8-DIBENZOPYRENE}                                 15
 DIBENZO[a,e]PYRENE {1,2,4,5-DIBENZOPYRENE}                                 16
 CYANOGEN CHLORIDE {CHLORINE CYANIDE}                                 17-18
 ACETONITRILE {ETHANENITRILE} [2]                                       17-18
 CHLOROBENZENE [2]                                                     19
 ACRYLONITRILE {2-PROPENENITRILE} [2]                                     20
 DICHLOROBENZENE {1,4-DICHLOROBENZENE}                                21-22
 CHLORONAPHTHALENE (1-) [2]                                           21-22
 CYANOGEN BROMIDE {BROMINE CYANIDE}                                   23-24
 DICHLOROBENZENE {1,2-DICHLOROBENZENE} [2]                            23-24
 DICHLOROBENZENE {1,3-DlCHLOROBENZENE} [2]                              25
 TRICHLOROBENZENE (1,3,5-TRICHLOROBENZENE) [2] [4]                       26-27
 TRICHLOROBENZENE (1,2,4-TRICHLOROBENZENE) [2]                         26-27
 TETRACHLOROBENZENE (1,2,3,5-TETRACHLOROBENZENE) [2] [4]                  20
 CHLOROMETHANE {METHYL CHLORIDE} [2]                                 29-30
 TETRACHLOROBENZENE (1,2,4,5-TETRACHLOROBENZENE)                       29-30
 PENTACHLOROBENZENE [2]                                              31-33
 HEXACHLOROBENZENE [2]                                               31-33
 BROMOMETHANE {METHYL BROMIDE} [2]                                   31-33
 TETRACHLORODIBENZO-p-DIOXIN (2,3,7,8-) {TCDD}                               34

 CLASS 2
 TOLUENE {METHYLBENZENE}  [2]                                            35
 TETRACHLOROETHENE [2]                                                 36
 CHLOROANILINE {CHLOROBENZENAMINE}                                      37
 DDE{1,1-DICHLORO-2,2-BIS(4-CHLOROPHENYLETHYLENE}                          38
 FORMIC ACID {METHANOIC ACID}                                          39-40
 PHOSGENE {CARBONYL CHLORIDE}                                        39-40
 TRICHLOROETHENE [2]                                                    41
 DIPHENYLAMINE {N-PHENYLBENZENAMINE}                                   42-44
 DICHLOROETHENE (1,1-) [2]                                              42-44
 FLUOROACETIC ACID                                                    42-44
 DIMETHYLBENZ[aJANTHRACENE (7,12-)                                        45
 ANILINE {BENZENAMINE}                                                 46-50
 FORMALDEHYDE {METHYLENE OXIDE}                                       46-50
 MALONONITRILE {PROPANEDINITRILE}                                       46-50
 METHYL CHLOROCARBONATE {CARBONOCHLORIDIC ACID, METHYL ESTER}         46-50
                                       109

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Table D-1.  Principal Hazardous Organic Constituent Thermal Stability Index (continued)

 Principal Hazardous Organic Constituent	Rank

 METHYL ISOCYANATE (METHYLCARBYLAMINE)                                 46-50
 AMINOBIPHENYL (4-) {[1,1'-BIPHENYL]-4-AMINE}                                  51
 NAPHTHYLAMINE (1 -)                                                     52-53
 NAPHTHYLAMINE (2-)                                                     52-53
 D1CHLOROETHENE (trans-1,2-) [2]                                            54
 FLUOROACETAMIDE  (2-)                                                   55-56
 PROPYN-1 -OL (2-) (PROPARGYL ALCOHOL}                                    55-56
 PHENYLENEDIAMINE (1,4) {BENZENEDIAMINE}                                  57-59
 PHENYLENEDIAMINE (1,2-) {BENZENEDIAMINE}                                 57-59
 PHENYLENEDIAMINE (1,3-) {BENZENEDIAMINE}                                 57-59
 BENZIDINE{[1,1'-BIPHENYL]-4,4'DIAMINE}                                     60-64
 ACRYLAMIDE {2-PROPENAMIDE}                                             60-64
 DIMETHYLPHENETHYLAMINE (alpha, alpha-)                                     60-64
 METHYL METHACRYLATE (2-PROPENOIC ACID, 2-METHYL-, METHYL ESTER}          60-64
 VINYL CHLORIDE (CHLOROETHENE)                                         60-64
 DICHLOROMETHANE {METHYLENE CHLORIDE} [2]                             65-66
 METHACRYLONITRILE {2-METHYL-2-PROPENENITRILE} [2]                       65-6 6
 DICHLOROBENZIDINE (3,3'-)                                                  67
 METHYLCHOLANTHRENE (3-)                                                 68
 TOLUENEDIAMINE (2,6-) {DIAMINOTOLUENE}                                   69-77
 TOLUENEDIAMINE (1,4-) {DIAMINOTOLUENE}                                   69-77
 TOLUENEDIAMINE (2,4-) {DIAMINOTOLUENE}                                   69-77
 TOLUENEDIAMINE (1,3-) {DIAMINOTOLUENE}                                   69-77
 TOLUENEDIAMINE (3,5-) {DIAMINOTOLUENE}                                   69-77
 TOLUENEDIAMINE (3,4-) {DIAMINOTOLUENE}                                   69-77
 CHLORO-1,3-BUTADIENE (2-) {CHLOROPRENE}                                 69-77
 PRONAMIDE {3,5-DICHLORO-N-[1,1-DIMETHYL-2-PROPYNYL] BENZAMIDE}            69-77
 ACETYLAMINOFLUORENE (2-) {ACETAMIDE,N-[9H-FLUOREN-2-YL]-}                  69-77

 CLASS 3
 DIMETHYLBENZIDINE (3,3'-)                                                  78
 n-PROPYLAMINE{1-PROPANAMINE}                                           79
 PYRIDINE [2]                                                             80
 PICOLINE (2-) {PYRIDINE, 2-METHYL-}                                         81-84
 DICHLOROPROPENE (1,1-) [2]                                               81-84
 THIOACETAMIDE {ETHANETHIOAMIDE}                                        81-84
 I^-TRICHLORO-I.I^-TRIFLUOROETHANE [2] [3]                             81-84
 BENZ[c]ACRIDINE {3,4-BENZACRIDINE}                                        85-88
 DICHLORODIFLUOROMETHANE  [2]                                         85-88
 ACETOPHENONE {ETHANONE, 1-PHENYL-} [2]                                 85-88
 TRICHLOROFLUOROMETHANE [2]                                          85-88
 DICHLOROPROPENE  (trans-1,2-)                                              89-91
 ETHYL CYANIDE {PROPIONITRILE} [2]                                        89-91
 BENZOQUINONE {1,4-CYCLOHEXADIENEDIONE}                                 89-91
 DIBENZ[a,h]ACRIDINE {1,2,5,6-DIBENZACRIDINE}                                 92-97
 DIBENZ[a,j]ACRIDINE {1,2,7,8-DIBENZACRIDINE}                                 92-97
 HEXACHLOROBUTADIENE (trans-1,3) [2]                                      92-97
 NAPHTHOQUINONE (1,4-) {1,4-NAPHTHALENEDIONE}                             92-97
 DIMETHYL PHTHALATE [2]                                                 92-97
 ACETYL CHLORIDE {ETHANOYL CHLORIDE} [2]                                92-97
 ACETONYLBENZYL-4-HYDROXYCOUMARIN (3-alpha-) {WARFARIN}                   98-99
 MALEIC ANHYDRIDE {2,5-FURANDIONE}                                        98-99
                                       110

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Table D-1.  Principal Hazardous Organic Constituent Thermal Stability Index (continued)

 Principal Hazardous Organic Constituent	Rank

 PHENOL (HYDROXYBENZENE)                                             100-101
 DIBENZO[c,g]CARBAZOLE (7H-) {3,4,5,6-DIBENZCARBAZOLE}                     100-101
 CHLOROPHENOL (2-)                                                       102
 CRESOL (1,3-) {METHYLPHENOL}                                             103
 CRESOL (1,4-) {METHYLPHENOL} [2]                                        104-105
 CRESOL (1,2-) {METHYLPHENOL}                                           1 04-1 05
 ACROLEIN {2-PROPENAL}                                                 106-107
 DIHYDROXY-ALPHA-[METHYLAMINO]METHYL BENZYL ALCOHOL (3,4-)               106-107
 METHYL ETHYL KETONE {2-BUTANONE} [2]                                 108-109
 DIETHYLSTILBESTEROL                                                   108-109
 BENZENETHIOL {THIOPHENOL} [2]                                          110
 RESORCINOL {1,3-BENZENEDIOL}                                            111
 ISOBUTYL ALCOHOL {2-METHYL-1-PROPANOL} [2]                              112
 CROTONALDEHYDE {2-BUTENAL} [2]                                       113-115
 DICHLOROPHENOL (2,4-)                                                  113-115
 DICHLOROPHENOL (2,6-)                                                  113-115
 METHYLACTONITRILE (2-) {PROPANENITRILE.2-HYDROXY-2-METHYL}               116-118
 ALLYL ALCOHOL {2-PROPEN-1 -OL}                                          116-118
 CHLOROCRESOL {4-CHLORO-3-METHYLPHENOL}                               116-118
 DIMETHYLPHENOL (2,4-)                                                     119

 CLASS 4
 CHLOROPROPENE 3-{ALLYL CHLORIDE} [2]                                   120
 DICHLOROPROPENE (cis-1,3-)                                               121-125
 DICHLOROPROPENE (trans-1,3-)                                             121-125
 TETRACHLOROETHANE (1,1,2,2-) [2]                                        1 21-1 25
 TRICHLOROPHENOL (2,4,5-)                                                121-125
 TRICHLOROPHENOL (2,4,6-)                                                121-125
 CHLOROETHANE (ETHYL CHLORIDE) [4] [5]                                      126
 DICHLOROPROPENE (2,3-)                                                 127-130
 HYDRAZINE (DIAMINE) [5]                                                 127-130
 BENZYL CHLORIDE {CHLOROMETHYLBENZENE} [2]                           127-130
 DIBROMOMETHANE {METHYLENE BROMIDE} [2]                              127-1 30
 DICHLOROETHANE (1,2-) [2]                                                 131
 MUSTARD GAS {bis[2-CHLOROETHYL]-SULFIDE}                               132-1 34
 NITROGEN MUSTARD                                                    132-134
 N,N-BIS(2-CHLOROETHYL)2-NAPHTHYLAMINE {CHLORNAPHAZINE}                 1 32-1 34
 DICHLOROPROPENE (3,3-)                                                   135
 DICHLORO-2-BUTENE (1,4-)                                                1 36-1 40
 TETRACHLOROPHENOL (2,3,4,6-)                                            136-140
 TETRACHLOROMETHANE {CARBONTETRACHLORIDE} [2]                       136-140
 BROMOACETONE {1-BROMO-2-PROPANONE}                                  136-1 40
 HEXACHLOROPHENE {2,2'-METHYLENEbis[3,4,6-TRICHLOROPHENOL]}              136-1 40
 DIOXANE (1,4-) {1,4-DIETHYLENE OXIDE} [2]                                    141
 CHLORAMBUCIL                                                           142
 NITROBENZENE [2]                                                        143
 CHLOROPROPIONITRILE (3-) {3-CHLOROPROPANENITRILE} [2]                   1 43-1 44
 DICHLORO-2-PROPANOL(1,1-)                                              145-146
 ODD {DICHLORODIPHENYLDICHLOROETHANE}                                1 45-1 46
 DICHLORO-2-PROPANOL (1,3-)                                                147
 PHTHALIC ANHYDRIDE {1,2-BENZENEDICARBOXYLIC ACID ANHYDRIDE}              148-1 50
 METHYL PARATHION                                                      1 48-1 50
                                       111

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Table D-1.  Principal Hazardous Organic Constituent Thermal Stability Index (continued)       '   •

 Principal Hazardous Organic Constituent      	•  	        :-            Rank •'•-'•

 NITROPHENOL (4-)                     . ,  ,                               148-150
 CHLORODIFLUOROMETHANE [2] [4]                                        151-153
 PENTACHLOROPHENOL                                       ,        !   15lr153
 HEXACHLOROCYCLOHEXANE {LINDANE} [2]                                 151-153
 DICHLOROFLUOROMETHANE [2] [4]                                        154-157
 DINITROBENZENE (1,3-)                    .                               154-157
 NITROANILINE{4-NITROBENZENAMINE}                                      154-157
 PENTACHLOROETHANE [2]                                               154-157
 DINITROBENZENE (1,4-)                            .                       158-161
 DINITROBENZENE (1,2-)                                                   158-161
 TRICHLOROETHANE (1,1,2-) [2]                                            158-161
 TRICHLOROMETHANE {CHLOROFORM} [2]                                  158-161
 DIELDRIN                  .•.•••••-•••••••                    162-164.
 ISODRIN                                                               163-1,6.4
 ALDRIN                                              : .                 162-164
 DICHLOROPROPANE (1,3-) (5]                                                i65
 NITROTOLUIDINE (5-) {BENZENAMINE.2-METHYL-5-NITRO-}   ,                    1,66-167
 CHLOROACETALDEHYDE                                                  166-167
 TRICHLOROPROPANE (1,2,3-) [2]                                           168-173
 DINITROTOLUENE (2,4-)                                                   168-173,
 DINITROTOLUENE (2,6-)                                                  .168-173
 HEXACHLOROCYCLOPENTADIENE                             .             168-173
 BENZAL CHLORIDE {ALPHA,  ALPHA-DICHLOROTOLUENE} (2]                    168-173
 DICHLORO-1-PROPANOL(2,3-)                                             168-1.73
 ETHYLENE OXIDE {OX1RANE} f5]                                              174,
 DICHLOROETHANE(1,1-) (ETHYLIDENE DICHLORIDE} [5]                         175-178
 DIMETHYLCARBAMOYLCHLORIDE   ,                                        175-178,
 GLYCIDYALDEHYDE{1-PROPANOL-2,3-EPOXY}                                 175-178
 DDT{DICHLORODIPHENYLTRICHLOROETHANE)   .       .          .         .   175-1,78
 DICHLOROPROPANE (1,2-) (PROPYLENE DICHLORIDE} (5} ...,.'.'                  179
 AURAMINE                                                             180-181
 HEPTACHLOR                                       '.,. .                  180-181
 DICHLOROPROPANE (1,1-) [5]                                                182
 CHLORO-2,3-EPOXYPROPANE(1-) {OXIRANE.2-CHLOROMETHYL-}                  183-186
 DINITROPHENOL (2,4-)                                                    183.-186
 bis(2-CHLOROETHYL)ETHER  [2]                                            183-186
 TRINITROBENZENE{1,3,5-TRINITROBENZENE}                                 183-186
 BUTYL-4,6-DINITROPHENOL (2-sec-) {DNBP}                                   187-,188
 CYCLOHEXYL-4.6-DINITROPHENOL (2-)                                       187-188
 bis(2-CHLOROETHOXY)METHANE                                            189-192
 CHLORAL {TRICHLOROACETALDEHYDE}                                      189-192
 TRICHLOROMETHANETHIOL                                            ,189-192
 DINITROCRESOL (4,6-) {PHENOL,2,4-DINITRO-6-METHYL-}                .'-..'   189-192
 HEPTACHLOR EPOXIDE                                    .                 193
 DIEPOXYBUTANE (1,2,3,4-) {2,2'-BIOXIRANE}                                     194

 CLASS 5
 BENZOTRICHLORIDE{TRICHLOROMETHYLBENZENE}                           195-196
 METHAPYRILENE                                               .      ..195-196
 PHENACETIN{N-[4-ETHOXYPHENYL]ACETAMIDE>                               t9.7r19'8
 METHYL HYDRAZINE [5]                                                   197-198
 DIBROMOETHANE (1,2-) {ETHYLENE DIBROMIDE)                            ',    199
                                       112

-------
Table D-1.  Principal Hazardous Organic Constituent Thermal Stability Index (continued)
 Principal Hazardous Organic Constituent	Rank
 AFLATOXINS                                                              200
 TRICHLOROETHANE (1,1,1-) {METHYL CHLOROFORM} [2]                         201
 HEXACHLOROETHANE [2]                                                 202-203
 BROMOFORM {TRIBROMOMETHANE} [2]                                    202-203
 CHLOROBENZILATE                                                       204-207
 ETHYL CARBAMATE (URETHAN) (CARBAMIC ACID, ETHYL ESTER)                 204-207
 ETHYL METHACRYLATE (2-PROPENOIC ACID, 2-METHYL-.ETHYL ESTER)          ,  204-207
 LASIOCARPINE                                                           204-207
 AMITROLE{lH-1,2,4-TRIAZOL-3-AMINE}                                       208-209
 MUSCIMOL {5-AMINOMETHYL-3-ISOAZOTOL}                                  208-209
 IODOMETHANE (METHYL IODIDE}                                              210
 DICHLOROPHENOXYACETIC ACID (2,4-) {2,4-D}            .                     211-213
 CHLORQETHYLVINYLETHER (2-) {ETHENE,[2-CHLOROETHOXYJ-} [2]              211-213
 METHYLENE BIS(2-CHLOROANILINE) (4,4-)                                     211-21-3
 DIBROMO-3-CHLOROPROPANE (1,2-)                                           214
 TETRACHLOROETHANE(1,1,1,2-)[2]                                           215
 DIMETHYLHYDRAZINE (1,1-) [5]                    .                          216-217
 N,N-DIETHYLHYDRAZINE{1,2-DIETHYLHYDRAZINE)                              216-217
 CHLOROMETHYLMETHYL ETHER {CHLOROMETHOXYMETHANE}                   21 8-220
 DIMETHYL-1-METHYLTHIO-2-BUTANONE,O-[(METHYLAMINO)-CARBONYL]             218-220
    OXIME (3,3-) {THIOFANOX}
 DIMETHYLHYDRAZINE (1,2-)                                                 218-220
 CHLORDANE (ALPHA AND GAMMA ISOMERS)                                    221
 bis(CHLOROMETHYL)ETHER {METHANE-OXYbis[2-CHLbRO-]}     "" '  '              222-223
 PARATHION [5]                                                           222-223
 DtCHLOROPROPANE (2,2-) [5]                                                 224
 MALEIC HYDRAZIDE{1,2-DIHYDRO-3,6-PYRIDAZINEDIONE)                          225
 BROMOPHENYL PHENYL ETHER (4-) {BENZENE, 1-BROMO-4-PHENOXY-}               226
 bis(2-CHLOROISOPROPYL)ETHER                                            227-228
 DIHYDROSAFROLE{1,2-METHYLENEDIOXY-4-PROPYLBENZENE}                   227-228
 METHYL METHANESULFONATE {METHANESUFONIC ACID, METHYL ESTER)            229
 PROPANE SULFONE (1,3-) {1,2-OXATHIOLANE,2,2-DIOXIDE}                          230
 SACCHARIN {1.2-BENZOISOTHIAZOLIN-3-ONE, 1,1-DIOXIDE)                          231
 METHYL-2-METHYLTHIO-PROPIONALDEHYDE-0-(METHYLCARBONYL)OXIME(2-)        232-233
 METHYOMYL                                                            232-233
 HEXACHLOROPROPENE [2]                                                  234
 PENTACHLORONITROBENZENE {PCNB}                                       235-239
 DIALLATE {S-(2,3-DICHLOROALLYL)DIISOPROPYL THIOCARBAMATE)                 235-239
 ETHYLENEIMINE {AZIRIDINE}                                               235-239
 ARAMITE                                                                235-239
 DIMETHOATE                                                            235-239
 TRICHLOROPHENOXYACETIC ACID (2,4,5-) {2,4,5-T}                              240-241
 TRICHLOROPHENOXYPROPIONIC ACID (2,4,5-) {2,4,5-TP} {SILVEX}                 240-241
 tris(2,3-DIBROMOPROPYL)PHOSPHATE                                          242
 METHYLAZIRIDINE (2-) {1,2-PROPYLENIMINE}                                  243-244
 METHOXYCHLOR                                                         243-244
 BRUCINE  {STRYCHNIDIN-10-ONE,2,3-DIMETHOXY-}                              245-246
 KEPONE                                               	        245-246
 ISOSAFROLE {1.2-METHYLENEDIOXY-4-ALLYLBENZENE}    '                      247-249
 SAFROLE{1,2-METHYLENE-4-ALLYLBENZENE)          ,        .                247-249
 tris(l-AZRlDINYL) PHOSPHINE SULFIDE                      '                  247-249
 DIMETHOXYBENZIDINE (3,3'-)                                                 250
 DIPHENYLHYDRAZINE (1,2-)                                                   251
 O,O-DIETHYLPHOSPHORIC AClD,0-p-NITROPHENYL ESTER                          252


                                        113

-------
Table D-1.  Principal Hazardous Organic Constituent Thermal Stability Index (continued)
 Principal Hazardous Organic Constituent	•      	Rank

 CLASS 6
 n-BUTYLBENZYL PHTHALATE [2J                                             253
 O,O-DIETHYL-O-2-PYRAZINYLPHOSPHOROTHIOATE                               254
 DIMETHYLAMINOAZOBENZENE                                               255
 DIETHYL PHTHALATE                                                    256-257
 O.O-DIETHYL-S-METHYL ESTER OF PHOSPHORIC ACID                         256-257
 O.O-DIETHYL S-[(ETHYLTHIO)METHYL]ESTER OF PHOSPHORODITHIOIC ACID        258-259
 CITRUS RED No. 2 {2-NAPHTHOL,1-[(2,5-DIMETHOXYPHENYL)AZO]}               258-259
 TRYPAN BLUE                                                            260
 ETHYL METHANESULFONATE (METHANESULFONIC ACID, ETHYL ESTER}           261-265
 DISULFOTON                                                          261-265
 DIISOPROPYLFLUOROPHOSPHATE {DFP}                                    261-265
 OAO-TRIETHYL PHOSPHOROTHIOATE                                      261-255
 Di-n-BUTYL PHTHALATE                                                  261-265
 PARALDEHYDE {2,4,6-TRIMETHYL-1,3,5-TRIOXANE} [5]                             266
 Di-n-OCTYL PHTHALATE [2]                                                  267
 OCTAMETHYLPYROPHOSPHORAMIDE {OCTAMETHYLDIPHOSPHORAMIDE}             268
 bis(2-ETHYLHEXYL)PHTHALATE                                            269-270
 METHYLTHIOURACIL                                                    269-270
 PROPYLTHIOURACIL                                                       271

 CLASS 7
 STRYCHNINE {STRYCHNIDIN-10-ONE}                                          272
 CYCLOPHOSPHAMIDE                                                   273-276
 NICOTINE {{S)-3-[1-METHYL-2-PYRROLIDINYL]PYRIDINE}                        273-276
 RESERPINE                                                            273-276
 TOLUIDINE HYDROCHLORIDE {2-METHYL-BENZENAMINE HYDROCHLORIDE}         273-276
 TOLYLENE DIISOCYANATE {1,3-DIISOCYANATOMETHYLBENZENE}                    277
 ENDRIN                                                                 278
 BUTANONE PEROXIDE (2-) (METHYL ETHYL KETONE. PEROXIDE}                     279
 TETRAETHYLPYROPHOSPHATE                                               280
 NITROGLYCERINE {JRINITRATE-1,2,3-PROPANETRIOL} [5]                           281
 TETRAETHYLDITHIOPYROPHOSPHATE                                         282
 ETHYLENEbisDITHIOCARBAMIC ACID                                           283
 TETRANITROMETHANE [5J                                                   284
 URACIL MUSTARD {5-[bis(2-CHLOROETHYL)AMINO]URACIL}                        285
 ACETYL-2-THIOUREA(1-) (ACETAMIDE,N-[AM)NOTHIOXOMETHYL]-}                286-290
 CHLOROPHENYL THIOUREA (1-) {THIOUREA, [2-CHLOROPHENYL]-}                286-290
 N-PHENYLTHIOUREA                                                    286-290
 NAPHTHYL-2-THIOUREA (1-) {THIOUREA, 1-NAPHTHALENYL-}                     286-290
 THIOUREA {THIOCARBAMIDE}                                             286-290
 DAUNOMYCIN                                                          291-292
 ETHYLENE THIOUREA {2-IMIDAZOLIDINETHIONE}                              291-292
 THIOSEMICARBAZIDE{HYDRAZINECARBOTHIOAMIDE}                          293-294
 MELPHALAN {ALANINE,3-[p-bis(2-CHLOROETHYL)AMINO]PHENYL-,L-}               293-294
 DITHIOBIURET (2,4-) (THIOIMIDODICARBONIC DIAMIDE}                         295-296
 THIURAM {bis[DIMETHYLTHIOCARBAMOYL]DISULFIDE}                          295-296
 AZASERINE {L-SERINE,DIAZOACETATE[ESTER]>                                 297
 HEXAETHYL  TETRAPHOSPHATE                                              298
 NITROGEN MUSTARD N-OXIDE                                             299-300
 NITROQUINOLINE-1-OXIDE (4-)                                             299-300
 CYCASIN {beta-D-GLUCOPYRANOSIDE,[METHYL-ONN-AZOXY]METHYL-}               301
                                       114

-------
Table D-1.  Principal Hazardous Organic Constituent Thermal Stability Index (continued)
 Principal Hazardous Organic Constituent	Rank	
 STREPTOZOTOCIN                                                       302
 N-METHYL-N'-NITRO-N-NITROSOGUANIDINE                                  303-318
 N-NITROSO-DI-ETHANOLAMINE{[2,2'-N!TROSOIMINO]bisETHANOL}                303-318
 N-NITROSQ-DI-N-BUTYLAMINE {N-BUTYL-N-NITROSO-1-BUTANAMINE}              303-31 8
 N-NITROSO-N-ETHYLUREA (N-ETHYL-N-NITROSOCARBAMIDE)                    303-31 8
 N-NITROSO-N-METHYLUREA{N-METHYL-N-NITROSOCARBAMIDE>                 303-318
 N-NITROSO-N-METHYLURETHANE                                          303-318
 N-NITROSODIETHYLAMINE{N-ETHYL-N-NITROSOETHANAMINE}                   303-318
 N-NITROSODIMETHYLAMINE{DIMETHYLNITROSAMINE}                         303-318
 N-NITROSOMETHYLETHYLAMINE (N-METHYL-N-NITROSOETHANAMINE)             303-31 8
 N-NITROSOMETHYLVINYLAMINE {N-METHYL-N-NITROSOETHENAMINE}             303-318
 N-NITROSOMORPHOLINE                                                 303-318
 N-NITRQSONORNICOTINE                                                303-318
 N-NITROSOPIPERIDINE{HEXAHYDRO-N-NITROSOPYRIDINE}                     303-318
 N-NITROSOSARCOSINE                                                  303-318
 NITROSOPYRROLIDINE (N-NITROSOTETRAHYDROPYRROLE)                     303-31 8
 DI-n-PROPYLNITROSAMINE {N-NITROSO-DI-n-PROPYLAMINE}                     303-318
 OXABICYCLO[2.2.1]HEPTANE-2,3-DICARBOXYLIC ACID (7-) {ENDOTHAL}               319
 ENDOSULFAN                                                           320

FOOTNOTES:

1. UNITS OF TEMPERATURE ARE DEGREES CELSIUS.

2. BOLDFACE INDICATES  COMPOUND THERMAL STABILITY IS "EXPERIMENTALLY  EVALUATED"
  (RANKING BASED ON UDRI EXPERIMENTAL DATA COUPLED WITH REACTION KINETIC THEORY).

3. NON-APPENDIX VIII  COMPOUND.

4. N.O.S. LISTING; RANKING IS PRESENTED BASED ON EITHER UDRI OR LITERATURE EXPERIMENTAL
  DATA COUPLED WITH REACTION KINETIC THEORY.

5. ITALICS INDICATE  COMPOUND  THERMAL STABILITY IS RANKED  BASED  ON  LITERATURE
  EXPERIMENTAL DATA COUPLED WITH REACTION KINETIC THEORY.
                                       115

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            Table D-2. Principal Hazardous Organic Constituent Thermal Stability Index - Alphabetized

             Principal Hazardous Organic Constituent	Rank

             ACETONITRILE {ETHANENITRILE} [2]                                        17-18
             ACETONYLBENZYL-4-HYDROXYCOUMARIN (3-alpha-) {WARFARIN}                   98-99
             ACETOPHENONE {ETHANONE, 1-PHENYL-} [2]                                85-88
             ACETYL CHLORIDE {ETHANOYL CHLORIDE} [2]                               92-97
             ACETYL-2-THIOUREA(1-) {ACETAMIDE,N-[AMINOTHIOXOMETHYL]-}                286-290
             ACETYLAMINOFLUORENE (2-) (ACETAMIDE,N-[9H-FLUOREN-2-YL]-}                  69-77
             ACROLEIN {2-PROPENAL}                                                106-107
             ACRYLAMIDE {2-PROPENAMIDE}                                            60-64
             ACRYLONITRILE {2-PROPENENITRILE} [2]                                     20
             AFLATOXINS                                                             200
             ALDRIN                                                              162-164
             ALLYL ALCOHOL {2-PROPEN-1-OL}                                        116-118
             AMINOBIPHENYL(4-){[1,1' BIPHENYLJ-4-AMINE}                                 51
             AMITROLE {1H-1,2,4-TRIAZOL-3-AMINE}                                     208-209
             ANILINE {BENZENAMINE}                                                  46-50
             ARAMITE                                                             235-239
             AURAMINE                                                            180-181
             AZASERINE (L-SERINE,DIAZOACETATE[ESTER]}                                 297
             BENZAL CHLORIDE {ALPHA, ALPHA-DICHLOROTOLUENE} [2]                  168-1 73
             BENZANTHRACENE(1,2-) {BENZ[a]ANTHRACENE}                                9
             BENZENE [2]                                                             3
             BENZENETHIOL {THIOPHENOL} [2]                                           110
             BENZIDINE {[1,1 '-BIPHENYL]-4,4' DIAMINE}                                     60-64
             BENZOQUINONE{1,4-CYCLOHEXADIENEDIONE}                                89-91
             BENZOTRICHLORIDE {TRICHLOROMETHYLBENZENE}                          195-196
             BENZO[a]PYRENE{1,2-BENZOPYRENE}                                        11
             BENZO[b]FLUORANTHENE {2,3-BENZOFLUORANTHENE}                           8
             BENZO[j]FLUORANTHENE {7,8-BENZOFLUORANTHENE}                            7.
             BENZYL CHLORIDE {CHLOROMETHYLBENZENE} [2]                          127-130
             BENZ[c]ACRIDINE{3,4-BENZACRIDINE}                                       85-88
             bis(2-CHLOROETHOXY)METHANE                                          1  89-1 92
             bis(2-CHLOROETHYL)ETHER [2]                                          183-186
             bis(2-CHLOROISOPROPYL)ETHER                                          227-228
             bis(2-ETHYLHEXYL)PHTHALATE                                            269-270
             bis(CHLOROMETHYL)ETHER  {METHANE-OXYbis[2-CHLORO-]}                    222-223
             BROMOACETONE{1-BROMO-2-PROPANONE}                                 136-140
             BROMOFORM {TRIBROMOMETHANE} [2]                                   202-203
             BROMOMETHANE {METHYL BROMIDE} [2]                                   31-33
             BROMOPHENYL PHENYL ETHER (4-) {BENZENE.1-BROMO-4-PHENOXY-}              226
             BRUCINE {STRYCHNIDIN-10-ONE,2,3-DIMETHOXY-}                             245-246
             BUTANONE PEROXIDE (2-) {METHYL ETHYL KETONE, PEROXIDE}                   279
I             BUTYL-4,6-DINITROPHENOL (2-sec-) {DNBP}                                  187-188
             CHLORAL {TRICHLOROACETALDEHYDE}                                     189-192
             CHLORAMBUCIL                                                          142
             CHLORDANE (ALPHA AND GAMMA ISOMERS)                                   221
             CHLORO-1.3-BUTADIENE (2-) {CHLOROPRENE}                                69-77
             CHLORO-2,3-EPOXYPROPANE (1-) {OXIRANE.2-CHLOROMETHYL-}                 183-186
             CHLOROACETALDEHYDE                                                 166-167
             CHLOROANILINE{CHLOROBENZENAMINE}                                      37
             CHLOROBENZENE [2]                                                      19
             CHLOROBENZILATE                                                     204-207
             CHLOROCRESOL {4-CHLORO-3-METHYLPHENOL}                             116-118
                                                   116

-------
Table D-2.  Principal Hazardous Organic Constituent Thermal Stability Index'- Alphabetized (continued)

 Principal Hazardous Organic Constituent	 "   	        Rank
 CHLORODIFLUOROMETHANE [2] [4]                                        151-153
 CHLOROETHANE (ETHYL CHLORIDE) (4] (5)                                      126
 CHLOROETHYLVINYLETHER (2-) {ETHENE,[2-CHLOROETHOXYJ-} [2]              211-213
 CHLOROMETHANE {METHYL CHLORIDE} [2]                                 29-30
 CHLOROMETHYLMETHYL ETHER {CHLOROMETHOXYMETHANE}                   218-220
 CHLORONAPHTHALENE (1-) [2]                                            21-22
 CHLOROPHENOL (2-)                                                       102
 CHLOROPHENYLTHIOUREA(I-)  {THIOUREA,[2-CHLOROPHENYL]-}                 286-290
 CHLOROPROPENE (3-) (ALLYL CHLORIDE} [2]        ,                          120
 CHLOROPROPIONITRILE (3-) {3-CHLOROPROPANENITRILE} [2]                  143-1 44
 CHRYSENE {1,2-BENZPHENANTHRENE}                                        10
 CITRUS RED No. 2 {2-NAPHTHOL,1-[(2,5-DIMETHOXYPHENYL)AZOl}                258-259
 CRESOL(1,2-){METHYLPHENOL}                                           104-105
 CRESOL(1,3-){METHYLPHENOL}                                             103
 CRESOL (1,4-) {METHYLPHENOL} [2]                                        104-105
 CROTONALDEHYDE {2-BUTENAL} [2]                                       113-115
 CYANOGEN BROMIDE (BROMINE CYANIDE}                                   23-24
 CYANOGEN CHLORIDE {CHLORINE CYANIDE}                    •              17-18
 CYANOGEN {ETHANEDINITRILE}                     '        ...               1
 CYCASIN{beta-D-GLUCOPYRANOSIDE,[METHYL-ONN-AZOXY] METHYL-}               301
 CYCLOHEXYL-4.6-DINITROPHENOL (2-)                                       1 87-1 88
 CYCLOPHOSPHAMIDE                                            '   -      273-276
 DAUNOMYCIN                                                           291-292
 DDD{DICHLORODIPHENYLDICHLOROETHANE}                                 145-146
 DDE{1,1-DICHLORO-2,2-BIS(4-CHLOROPHENYLETHYLENE}                          38
 DDT{DICHLORODIPHENYLTRICHLOROETHANE}                                175-178
 Di-n-BUTYL PHTHALATE                                                   261-265
 Di-n-OCTYL PHTHALATE [2]                                                 267
 DI-n-PROPYLNITROSAMINE{N-N1TROSO-DI-n-PROPYLAMINE}                      303-318
 DIALLATE {S-(2,3-DICHLOROALLYL)DIISOPROPYL THIOCARBAMATE)                235-239
 DIBENZO[a,e]PYRENE{1,2,4,5-DIBENZOPYRENE}                                 16
 DIBENZO[a,hlPYRENE{1,2,5,6-DIBENZOPYRENE}                  ,,..""•         14
 DIBENZO[a,i]PYRENE {1,2,7,8-DIBENZOPYRENE}                                  15
 DIBENZO[c,g]CARBAZOLE (7H-) {3,4,5,6-DIBENZCARBAZOLE}                      100-101
 DIBENZ[a,h]ACRIDINE{1,2,5,6-DIBENZACRIDINE}                                92-97
 DIBENZ[a,h]ANTHRACENE{1,2,5,6-DIBENZANTHRACENE}   s                        12
 DIBENZ[a,j]ACRIDINE{1,2,7,8-DIBENZACRIDINE}        .  .           :           92-97
 DIBROMO-3-CHLOROPROPANE (1,2-)                                      ••    214
 DIBROMOETHANE(1,2-) {ETHYLENE DIBROMIDE}                                 199
 DIBROMOMETHANE {METHYLENE BROMIDE} [2]                              127-130
 DICHLORO-1-PROPANOL (2,3-)                                              168-173
 DICHLORO-2-BUTENE(1,4-)                                                 136-140
 DICHLORO-2-PROPANOL(1,1-)                                              145-146
 DICHLORO-2-PROPANOL(1,3-)                                                147
 DICHLOROBENZENE {1,2-DICHLOROBENZENE} [2]                            23-24
 DICHLOROBENZENE {1,3-DICHLOROBENZENE} [2]                              25
 DICHLOROBENZENE {1,4-DICHLOROBENZENE}                                 21-22
 DICHLOROBENZIDINE (3,3'-)                                                  67
 DICHLORODIFLUOROMETHANE [2]                                         85-88
 DICHLOROETHANE (1,1-) {ETHYL/DENE DICHLORIDE} [5]                          175.-1 78
 DICHLOROETHANE (1,2-) [2]                                                 131
 DICHLOROETHENE (1,1-) [2]                                               42-44
                                       117

-------
Table D-2.  Principal Hazardous Organic Constituent Thermal Stability Index - Alphabetized (continued)
 Principal Hazardous Organic Constituent	 Rank
 DICHLOROETHENE (trans-1,2-) [2]                                              54
 DICHLOROFLUOROMETHANE [2] [4]                                         154-157
 DICHLOROMETHANE {METHYLENE CHLORIDE} [2]                             65-66
 DICHLOROPHENOL (2,4-)                                                   113-115
 DICHLOROPHENOL (2,6-)                                                   113-115
 DICHLOROPHENOXYACETIC ACID (2,4-) {2,4-D}                                 211-213
 DICHLOROPROPANE(1,1-)[5]                                                 182
 DICHLOROPROPANE (1,2-) {PROPYLENE DICHLORIDE} [5]                          179
 DICHLOROPROPANE(1,3-)[5]                                                 165
 DICHLOROPROPANE (2,2-) [51                                                 224
 DICHLOROPROPENE (1,1-) [2]                                               81-84
 DICHLOROPROPENE (2,3-)                                                 127-130
 DICHLOROPROPENE (3,3-)                                                   135
 DICHLOROPROPENE (cis-1,3-)                                               121-125
 DICHLOROPROPENE (trans-1,2-)                                              89-91
 DICHLOROPROPENE (trans-1,3-)                                             121-125
 DIELDRIN                                                               161-163
 DIEPOXYBUTANE (1,2,3,4-) {2,2'-BIOXlRANE}                                     194
 DIETHYL PHTHALATE                                                     256-257
 DIETHYLSTILBESTEROL                                                   108-109
 DIHYDROSAFROLE {1.2-METHYLENEDIOXY-4-PROPYLBENZENE}                   227-228
 DIHYDROXY-ALPHA-[METHYLAMINO]METHYL BENZYL ALCOHOL (3,4-)               106-107
 DIISOPROPYLFLUOROPHOSPHATE {DFP}                                     261-265
 DIMETHOATE                                                            235-239
 DIMETHOXYBENZIDINE (3,3'-)                                                 250
 DIMETHYL PHTHALATE [2]                                                  92-97
 DIMETHYL-1-METHYLTHIO-2-BUTANONE,0-[(METHYLAMINO)-CARBONYL]             218-220
   OXIME (3,3-) {THIOFANOX}
 DIMETHYLAMINOAZOBENZENE                                                255
 DIMETHYLBENZIDINE (3,3'-)                                                   78
 DIMETHYLBENZ[a]ANTHRACENE (7,12-)                                         45
 DIMETHYLCARBAMOYLCHLORIDE                                            175-178
 DIMETHYLHYDRAZINE (1,1-) [5]                                              216-217
 DIMETHYLHYDRAZINE (1,2-)                                                 218-220
 DIMETHYLPHENETHYLAMINE (alpha, alpha-)                                     60-64
 DIMETHYLPHENOL (2,4-)                                                     119
 DINITROBENZENE(1,2-)                                                    158-161
 DINITROBENZENE(1,3-)                                                    154-157
 DINITROBENZENE(1,4-)                                                    158-161
 DINITROCRESOL (4,6-) {PHENOL,2,4-D!NITRO-6-METHYL-}                         1 89-192
 DINITROPHENOL (2,4-)                                                     183-186
 DINITROTOLUENE (2,4-)                                                    168-173
 DINITROTOLUENE (2,6-)                                                    168-173
 DIOXANE (1,4-) {1,4-DIETHYLENE OXIDE} [2]                                     141
 DIPHENYLAMINE {N-PHENYLBENZENAMINE}                                    42-44
 DIPHENYLHYDRAZINE (1,2-)                                                   251
 DISULFOTON                                                            261-265
 DITHIOBIURET (2,4-) (THIOIMIDODICARBONIC DIAMIDE}                           295-296
 ENDOSULFAN                                                              320
 ENDRIN                                                                  278
 ETHYL CARBAMATE {URETHAN} {CARBAMIC ACID, ETHYL ESTER}                 204-207
 ETHYL CYANIDE {PROPIONITRILE} [2]                                        89-91
 ETHYL METHACRYLATE {2-PROPENOIC ACID, 2-METHYL-.ETHYL ESTER}            204-207
                                        118

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Table D-2.  Principal Hazardous Organic Constituent Thermal Stability Index - Alphabetized (continued)

 Principal Hazardous Organic Constituent	Rank

 ETHYL METHANESULFONATE {METHANESULFONIC ACID, ETHYL ESTER}           261-265
 ETHYLENE OXIDE {OXIRANE} [5]                                             174
 ETHYLENE THIOUREA {2-IMIDAZOLIDINETHIONE}                              291-292
 ETHYLENEbisDITHIOCARBAMIC ACID                                          283
 ETHYLENEIMINE {AZIRIDINE}                                              235-239
 FLUORANTHENE {BENZO[j,k]FLUORENE}                                       6
 FLUOROACETAMIDE (2-)                                                   55-56
 FLUOROACETIC ACID                                                     42-44
 FORMALDEHYDE (METHYLENE OXIDE}                                       46-50
 FORMIC ACID {METHANOIC ACID}                                           39-40
 GLYCIDYALDEHYDE {1-PROPANOL-2.3-EPOXY}                                1 75-1 78
 HEPTACHLOR                                                         180-181
 HEPTACHLOR EPOXIDE                                                    193
 HEXACHLOROBENZENE [2]                                                31-33
 HEXACHLOROBUTADIENE (trans-1,3) [2]                                     92-97
 HEXACHLOROCYCLOHEXANE {LINDANE} [2]                                 151-153
 HEXACHLOROCYCLOPENTADIENE                                          168-173
 HEXACHLOROETHANE [2]                                                202-203
 HEXACHLOROPHENE{2,2'-METHYLENEbis[3,4,6-TRICHLOROPHENOL]}              136-140
 HEXACHLOROPROPENE [2]                                                 234
 HEXAETHYL TETRAPHOSPHATE                                              298
 HYDRAZINE (DIAMINE)                                                   127-130
 HYDROGEN CYANIDE {HYDROCYANIC ACID} [2]                                 2
 INDENO(1,2,3-cd)PYRENE{1,10-(1,2-PHENYLENE)PYRENE}                          13
 IODOMETHANE {METHYL IODIDE}                                            210
 ISOBUTYL ALCOHOL {2-METHYL-1-PROPANOL} [2]                              112
 ISODRIN                                                              162-164
 ISOSAFROLE {1.2-METHYLENEDIOXY-4-ALLYLBENZENE}                         247-249
 KEPONE                                                              245-246
 LASIOCARPINE                                                         204-207
 MALEIC ANHYDRIDE {2,5-FURANDIONE}                                       98-99
 MALEIC HYDRAZIDE {1,2-DIHYDRO-3,6-PYRIDAZINEDIONE}                          225
 MALONONITRILE {PROPANEDINITRILE}                                       46-50
 MELPHALAN {ALANINE,3-[p-bis(2-CHLOROETHYL)AMINO]PHENYL-,L-}               293-294
 METHACRYLONITRILE {2-METHYL-2-PROPENENITRILE} [2]                       65-66
 METHAPYRILENE                                                        195-196
 METHOXYCHLOR                                                        243-244
 METHYL CHLOROCARBONATE {CARBONOCHLORIDIC ACID, METHYL ESTER}          46-50
 METHYL ETHYL KETONE {2-BUTANONE} [2]                                 108-109
 METHYL HYDRAZINE [5]                                                  197-198
 METHYL ISOCYANATE {METHYLCARBYLAMINE}                                 46-50
 METHYL METHACRYLATE {2-PROPENOIC ACID, 2-METHYL-, METHYL ESTER}          60-64
 METHYL METHANESULFONATE {METHANESULFONIC ACID, METHYL ESTER}           229
 METHYL PARATHION                                                     148-150
 METHYL-2-METHYLTHIO-PROPIONALDEHYDE-0-(METHYLCARBONYL)OXIME(2-)        232-233
 METHYLACTONITRILE (2-) {PROPANENITRILE.2-HYDROXY-2-METHYL}               116-118
 METHYLAZIRIDINE (2-) {1,2-PROPYLENIMINE}                                 243-244
 METHYLCHOLANTHRENE (3-)                                                68
 METHYLENE BIS(2-CHLOROANILINE) (4,4-)                                    211-213
 METHYLTHIOURACIL                                                     269-270
 METHYOMYL                                                           232-233
 MUSCIMOL{5-AMINOMETHYL-3-ISOAZOTOL}                                 208-209
                                       119

-------
Table D-2.  Principal,Hazardous Organic Constituent Thermal Stability Index - Alphabetized (continued)
 Principal Hazardous Organic Constituent                                         Rank ,.
 MUSTARD GAS (bis[2-CHLOROETHYL]-SULFIDE)        :
 N,N-BIS(2-CHLOROETHYL)2-NAPHTHYLAMINE (CHLORNAPHAZINE)
 N.N-DIETHYLHYDRAZINE (1,2-DIETHYLHYDRAZINE)
 n-BUTYLBENZYL PHTHALATE [2]
 N-METHYL-N'-NITRO-N-NITROSOGUANIDINE
 N-NITROSO-DI-ETHANOLAMINE{[2,2'-NITROSOIMINQ]bisETHANOL)
 N-NITROSO-DI-N-BUTYLAMINE (N-BUTYL-N-NITROSO-1 -BUTANAMINE)
 N-NITROSO-N-ETHYLUREA {N-ETHYL-N-NITROSOCARBAMIDE}     • ,   •  •
 N-NITROSO-N-METHYLUREA(N-METHYL-N-NITROSOCARBAMIDE)
 N-NITROSO-N-METHYLURETHANE
 N-NITROSODIETHYLAMINE (N-ETHYL-N-NITROSOETHANAMINE)
 N-NITROSODIMETHYLAMINE {DIMETHYLNITROSAMINE}.    .         •
 N-NITROSOMETHYLETHYLAMINE {N-METHYL-N-NITROSOETHANAMINE}
 N-NITROSOMETHYLVINYLAMINE{N-METHYL-N-NITROSOETHENAMINE>
 N-NITROSOMORPHOLINE
 N-NITROSONORNICOTINE
 N-NITROSOPIPERIDINE {HEXAHYDRO-N-NITROSOPYRIDINE}.   •
 N-NITROSOSARCOSINE
 N-PHENYLTHIOUREA
 n-PROPYLAMINE {1-PROPANAMINE}
 NAPHTHALENE [2]
 NAPHTHOQUINONE (1,4-) {1,4-NAPHTHALENEDIONE}
 NAPHTHYL-2-THIOUREA(1-){THIOUREA,1-NAPHTHALENYL-}    .
 NAPHTHYLAMINE (1-)
 NAPHTHYLAMINE (2-)
 NICOTINE {(S)-3-[1-METHYL-2-PYRROLIDINYL]PYRIDlNE)
 NITROANILINE{4-NITROBENZENAMINE)
 NITROBENZENE [2]
 NITROGEN MUSTARD                                   ;
 NITROGEN MUSTARD N-OXIDE
 NITROGLYCERINE {JRINITRATE-1,2,3-PROPANETRIOL} [5]
 NITROPHENOL (4-)
 NITROQUINOLINE-1-OXIDE (4-)
 NITROSOPYRROLIDINE (N-NITROSOTETRAHYDROPYRROLE)
 NITROTOLUIDINE (5-) {BENZENAMINE.2-METHYL-5-NITRO-}
 O,O,O-TRIETHYL PHOSPHOROTHIOATE
 O.O-DIETHYL S-[(ETHYLTHIO)METHYL]ESTER OF PHOSPHORODITHIOIC ACID
 O.O-DIETHYL-O-2-PYRAZINYL PHOSPHOROTHIOATE
 O.O-DIETHYL-S-METHYL ESTER OF PHOSPHORIC ACID
 O.O-DIETHYLPHOSPHORIC ACID.O-p-NITROPHENYL ESTER
 OCTAMETHYLPYROPHOSPHORAMIDE {OCTAMETHYLDIPHOSPHORAMIDE}
 OXABICYCLO[2.2.1]HEPTANE-2,3-DICARBOXYLIC ACID (7-) {ENDOTHAL}
 PARALDEHYDE {2,4,6-TRIMETHYL-1,3,5-TRIOXANE} [5]     <
 PARATHION  [5]
 PENTACHLOROBENZENE [2J
 PENTACHLOROETHANE [2]
 PENTACHLORONITROBENZENE {PCNB}
 PENTACHLOROPHENOL
 PHENACETIN {N-[4-ETHOXYPHENYL]ACETAMIDE>
 PHENOL {HYDROXYBENZENE}
 PHENYLENEDIAMINE(1,2-) (BENZENEDIAMINE)          , .  ,
 PHENYLENEDIAMINE (1,3-) {BENZENEDIAMINE}
 132-134
 132-134
 216-217
   253
 303-318
 303-318
 303-318
 303-318
 303-318
 303-318
 303-318
 303-318
 303-318
 303-318
 303-318
 303-3 l^
 303-31,8;
 303-318
 286-290^
 92-97
286-290
 52-53
 52-53,
273-276
154-157
  143
132^134
299-300
.. 281
148-150
299-300
303-318
166-167.
261-26.5
258-259
  254 s  -
256-257
  252
  268 ,
 7 319 ••:.>:•.
  266
222-223
 31-33,
154-157
235-239
151-153
197-198
100-101
 57-59
 57-59
                                       120

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Table D-2.  Principal Hazardous Organic Constituent Thermal Stability Index - Alphabetized  (continued)
 Principal Hazardous Organic Constituent	Rank

 PHENYLENEDIAMINE (1,4) {BENZENEDIAMINE}                                 57-59
 PHOSGENE (CARBONYL CHLORIDE}                                        39-40
 PHTHALIC ANHYDRIDE {1,2-BENZENEDICARBOXYLIC ACID ANHYDRIDE)             1 48-1 50
 PICOLINE (2-) (PYRIDINE, 2-METHYL-}                                        81-84
 PRONAMIDE{3,5-DICHLORO-N-[1,1-DIMETHYL-2-PROPYNYL] BENZAMIDE)           69-77
 PROPANE SULFONE (1,3-) (1,2-OXATHIOLANE,2,2-DIOXIDE}                        230
 PROPYLTHIOURACIL                                                      271
 PROPYN-1 -OL (2-) {PROPARGYL ALCOHOL}                                   55-56
 PYRIDINE [2]                                                             80
 RESERPINE                                                            273-276
 RESORCINOL{1,3-BENZENEDIOL>                                            111
 SACCHARIN {1.2-BENZOISOTHIAZOLIN-3-ONE, 1,1-DIOXIDE}                        231
 SAFROLE{1,2-METHYLENE-4-ALLYLBENZENE}                                 247-249
 STREPTOZOTOCIN                                                        302
 STRYCHNINE {STRYCHNIDIN-10-ONE}                                         272
 SULFUR HEXAFLUORIDE [31                                                  4
 TETRACHLOROBENZENE (1,2,3,5-TETRACHLOROBENZENE) [2] [4]                  20
 TETRACHLOROBENZENE (1,2,4,5-TETRACHLOROBENZENE)                       29-30
 TETRACHLORODIBENZO-p-DIOXIN (2,3,7,8-) {TCDD}                               34
 TETRACHLOROETHANE (1,1,1,2-) [2]                                         215
 TETRACHLOROETHANE (1,1,2,2-) [2]                                        121-125
 TETRACHLOROETHENE [2]                                                  36
 TETRACHLOROMETHANE {CARBONTETRACHLORIDE} [2]                       136-140
 TETRACHLOROPHENOL (2,3,4,6-)                                            136-140
 TETRAETHYLDITHIOPYROPHOSPHATE                                         282
 TETRAETHYLPYROPHOSPHATE                                              280
 TETRANITROMETHANE [5]                                                   284
 THIOACETAMIDE {ETHANETHIOAMIDE}                                       81-84
 THIOSEMICARBAZIDE{HYDRAZINECARBOTHIOAMIDE}                          293-294
 THIOUREA {THIOCARBAMIDE}                                             286-290
 THIURAM  {bis[DIMETHYLTHIOCARBAMOYL]DISULFIDE}                          295-296
 TOLUENE {METHYLBENZENE} [2]                                           35
 TOLUENEDIAMINE (1,3-) {DIAMINOTOLUENE}                                   69-77
 TOLUENEDIAMINE (1,4-) {DIAMINOTOLUENE}                                   69-77
 TOLUENEDIAMINE (2,4-) {DIAMINOTOLUENE}                                   69-77
 TOLUENEDIAMINE (2,6-) {DIAMINOTOLUENE}                                   69-77
 TOLUENEDIAMINE (3,4-) {DIAMINOTOLUENE}                                   69-77
 TOLUENEDIAMINE (3,5-) {DIAMINOTOLUENE}                                   69-77
 TOLUIDINE HYDROCHLORIDE {2-METHYL-BENZENAMINE HYDROCHLORIDE}         273-276
 TOLYLENE DIISOCYANATE {1,3-DIISOCYANATOMETHYLBENZENE}                   277
 TRICHLOROBENZENE (1,2,4-TRICHLOROBENZENE) [2]                          26-27
 TRICHLOROBENZENE (1,3,5-TRICHLOROBENZENE) [2] [4]                       26-27
 TRICHLOROETHANE (1,1,1-) {METHYL CHLOROFORM} [2]                        201
 TRICHLOROETHANE (1,1,2-) [2]                                            158-161
 TRICHLOROETHENE [2]                                                   41
 TRICHLOROFLUOROMETHANE [2]                                          85-88
 TRICHLOROMETHANE {CHLOROFORM} [2]                                  195-196
 TRICHLOROMETHANETHIOL                                               189-192
 TRICHLOROPHENOL (2,4,5-)                                               121-125
 TRICHLOROPHENOL (2,4,6-)                                               121-125
 TRICHLOROPHENOXYACETIC ACID (2,4,5-) {2,4,5-T}            '                 240-241
 TRICHLOROPHENOXYPROPIONIC ACID (2,4,5-) {2,4,5-TP} {SILVEX}                 240-241
                                       121

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Table D-2.  Principal Hazardous Organic Constituent Thermal Stability Index  - Alphabetized (continued) ^
 Principal Hazardous Organic Constituent	Rank	

 TRICHLOROPROPANE (1,2,3-) [2]                                           168-1 73
 TRICHLORO-(1,2,2)-TRIFLUOROETHANE (1,1,2) [2] [3]                             81-84
 TRINITROBENZENE{1,3,5-TRINITROBENZENE}                                 183-186
 tris(l-AZRIDINYL) PHOSPHINE SULFIDE                   -                     247-249
 tris(2,3-DIBROMOPROPYL)PHOSPHATE                                          242
 TRYPANBLUE                                                             260
 URACIL MUSTARD {5-[bis(2-CHLOROETHYL)AMINO]URACIL}                         285
 VINYL CHLORIDE (CHLOROETHENE)                                           60-64

FOOTNOTES:

1. UNITS OF TEMPERATURE ARE DEGREES CELSIUS.

2. BOLDFACE INDICATES COMPOUND  THERMAL  STABILITY  IS "EXPERIMENTALLY  EVALUATED"
  (RANKING BASED ON UDRI EXPERIMENTAL DATA COUPLED WITH REACTION KINETIC THEORY).

3. NON-APPENDIX VIII COMPOUND.

4. N.O.S. LISTING; RANKING IS  PRESENTED BASED ON EITHER UDRI OR LITERATURE EXPERIMENTAL
  DATA COUPLED WITH REACTION KINETIC THEORY.

5. ITALICS  INDICATE COMPOUND THERMAL  STABILITY  IS  RANKED BASED ON  LITERATURE
  EXPERIMENTAL DATA COUPLED WITH REACTION KINETIC THEORY.
                                        122

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Table D-3.  Appendix Vlll Thermal Stability Classes
            Class               Compound Ranking
                         T9g(2) Range
              1
              2
              3
              4
              5
              6
              7
  1-34
 35-77
 78-119
120-193
194-252
253-271
272-320
1,590-900
 895-800
 790-705
 695-604
 600-425
 415-360
 320-100
                                            123

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                                            APPENDIX £
                          Energy and Mass Balance Computer Program
 E.1 Energy and Mass Balance

 A computer program has been  developed by Energy
 and Environmental  Research  Corporation (EER)
 under  contract to the EPA to  perform energy  and
 mass  balance calculations  on  hazardous waste
 incinerators.

 The calculations  are  performed for a  single zone
 incinerator or for  an incinerator  system composed of
 single  zones in series. The composition of gases  and
 solids  in a zone is assumed to be the same as  the
 exit composition--that of  complete  reaction;  the
 temperature in a zone is assumed to be the same as
 the exit temperature; and the residence time within a
 zone is  assumed to  be  the  mean residence time.
 Products of one zone  enter the  next zone at the  exit
 temperature of the first zone. In  cases  where there is
 a significant heat loss between the incinerator units, a
 transition zone is  included between the units to allow
 the  products to enter the  second  unit  at  a lower
 temperature than they exit the first.

 This section discusses the  components of the June
 1987 version of the EER  program and the principles,
 assumptions, and  limitations involved.  Because  the
 inputs  and outputs of the model are in  English units,
 this section is written in English units.

 E.1.1 Input
 Inputs  to the energy and  mass  balance  include feed
 rate, temperature,  heating value, heat  capacity, heat
 of vaporization, and composition of all input streams
 to each unit including wastes,  fuels, water,  air, and
 oxygen; incinerator design specifications including  the
 thickness and  conductivity  of  the refractory,  the
 volume of the unit, the area of the refractory and any
 cooled surfaces, and the outer shell temperature; and
 the air pollution  control  equipment (APCE)  design
 specifications including  gas  volumetric  capacity, acid
 capacity, quench  water capacity  and  temperature,
 and  the  temperature  to  which the gas must  be
 quenched.  Table  E-1  shows a  typical  blank input
form.

 Feed rates are in  the form of mass flows.  Preheat
denotes the temperature at which a stream enters  the
 incinerator. Proximate analysis is a standard analytical
 procedure  used to characterize fuels  consisting  of
 mass percentages of fixed carbon, volatiles, ash, and
 moisture. Elemental analysis consists of the dry mass
 percentages  of  carbon,  hydrogen,  nitrogen,  sulfur,
 ash,  oxygen  and  chlorine.  Halogens other than
 chlorine  are  treated as chlorine by multiplying their
 mass  percentage  by the ratio  of  atomic  weight  of
 chlorine  to  the  atomic weight  of  the  halogen and
 renormalizing so that the total  mass  percentage  is
 100.

 Heating value is input as the higher or  gross heating
 value,  the way it is typically measured  and reported.
 The higher heating value (HHV) is defined as the heat
 of complete  combustion of the fuel/waste at 77° F
 (298°K)  with all  product water in liquid form and all
 product chlorine in the form  of HO.  If the  heating
 value  is  unknown, it can  be  estimated  from the
 fuel/waste composition by equation 1:
HHV = 1.8 [(100 - ASH - MOISTURE)/!00]
     X {83.2C + 275.15H + 25.0S
     + 15.0N - 25.8(0)
     - 568.4 [1 - exp(-0.582 Cl/C)]} Btu/lb
(1)
where ASH and MOISTURE  are  mass percentages
on a  wet  as-fired basis  and C, H, S, N, Cl, and O
are mass percentages on a  dry  ash-free  basis. To
convert from a dry basis to a dry  ash-free basis,
divide  each mass fraction by [100 - ASHwet/(100  •
MOISTURE)]. Note that equation 1 includes the  heat
of solution of HCI in the value  for the high heating
value;  this is  not  a  common  usage.  Normal
nomenclature defines high heating value as the  sum
of the waste's (or fuel's) lower heating value (LHV)
and the latent  heat  of  vaporization  of  the water
formed in the combustion  process.  For highly
chlorinated material,  however, the  heat of solution of
the HCI also becomes significant and  is,  therefore,
included here.

Heat  capacity  is only  important  if the  preheat
temperature is significantly different  from  the
reference  temperature of  77°F (298°K). The  heat
capacity depends  on the composition:  aqueous
wastes  generally have a heat capacity around  1.0,
                                                125

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              Table E-1.    Energy and Mass Balance Input Data.
ro
en

LIQUID WASTE
SOLID WASTE
PRIMARY FUEL
SECONDARY FUEL
PRIMARY AIR
SECONDARY AIR
WATER
OXYGEN
ASH DROPOUT
HAZARDOUS
COMPOUNDS



FEED RATE
(LB/H)













PREHEAT
(°R








PROXIMATE ANALYSIS (PERCENT)
(AS RECEIVED)
FIXED
CARBON






VOLAT1LES




ASH





MOISTURE




HEATNG
VALUE
(HIGHER
ASRECVD)
(BTU/LB)




HEAT
CAPACrTY
(AS
RECEIVED)
(BTU/LB)




HEAT OF
VAPORI-
ZATION
(DRY)
(BTU/LB)




ELEMENTAL ANALYSIS
(DRY PERCENT)
C




H




N




S




ASH O Cl





DESIGN SPECIFICATIONS
REFRACTORY THICKNESS (IN)
REFRACTORY CONOUCTIVrTY (BTU INM FT2 °F)
UNIT VOLUME (FT3)
REFRACTORY SURFACE AREA (FT 2)
COOLED SURFACE AREA (FT2)
OUTER SHELL TEMPERATURE ( ° F)
PCC






sec







                                                                                             APCD
GASCAPAOTY(SCFM)
STACK GAS TEMPERATURE ( ° F)
HCI CAPACITY (LB/H)
QUENCH WATER CAPACITY (GPM)
QUENCH WATER TEMPERATURE (
OF)






-------
 organic wastes around 0.4, and  inert solids around
 0.2  Btu/lb-°F.

 Heat of vaporization is generally incorporated into the
 heating value. If the heating value is given  for the
 fuel/waste in liquid form, the heat  of vaporization
 should  be entered as zero. Heat of  vaporization is
 only for the dry fuel/waste. Moisture  vaporization is
 automatically taken into account in the  program.

 The refractory thickness is  the distance between the
 inside and  the. outside  wall  of  the  refractory.  The
 refractory conductivity is the effective  conductivity of
 the  refractory  as if  it  were  a flat slab of uniform
 composition. For a cylindrical incinerator, the effective
 thermal conductivity can be calculated from equation
 2:
            K'X t
      ff
     eff
          r.ln  -
                  (2)
where Keff and K are the effective and actual thermal
conductivities, t0 is the overall thickness, and r0 and
rj  are the outer and inner refractory  radii. For a
cylindrical  incinerator  with  layers of  refractory, the
composite thermal conductivity  can  be  calculated
from equation 3:
                          t
   . ,
   eff
             In  -
                   (3)
                   ' +
                        K2
+ ...
        K
For a flat wall with layers of refractory, the composite
thermal conductivity can be calculated from equation
4:
                       t
        Keff =
                 (4)
                — H	

                Kl    K2
 K
For an incinerator with sections or walls with different
refractories  such  as  an  incinerator  with  different
insulation on  its end walls,  the effective  thermal
conductivity is the  area-weighted  average  of  the
individual conductivities as calculated in equation 5:
             K1A1
V0+ ...K A
2       n  n
                 (5)
 The volume of the unit is the inside volume, and the
 refractory surface area is the inside refractory surface
 area. In cases where two units connect with an open
 surface in  between rather than a wall, the area of the
 interface is added to the refractory surface area. The
 cooled  surface area is the optical  area of any cooled
 surfaces; thus, for a cooled plate, it is the area of one
 side of  the plate; for a cooled tube against the wall, it
 is the length of the tube times the  diameter;  and for a
 cooled tube within the flow, it is the length of the tube
 times twice its diameter. The outer shell temperature
 is only important if the heat balance on the outer shell
 has been disabled. Otherwise, the  program calculates
 outer shell temperature.

 The APCD gas  capacity is  the specified maximum
 capacity of the APCD, which is usually dictated by the
 capacity of the  ID fan.  The  HCI  capacity is the
 capacity of the system to remove  HCI. The available
 quench water is usually  dictated by pump size. The
 quench water temperature serves  as  a  limit
 temperature  below which  the   gas  cannot be
 quenched. The  stack  gas  temperature  is the
 temperature of effluent in the stack.

 £.7.2 Mass Balance
 The mass balance calculates  the  products  of
 complete combustion of  the mixture of all the inputs
 to each unit of the incinerator. Species considered
 include  C,  H,  N, 0, S, Cl, Ash, H2O,  C>2, C02, N2,
 SC-2, and HCI.

 Each  input stream  is broken  down into the  mass
 flows of its individual components by equation 6:
                                                        m. = m .     x mass fraction.
                                                          i     stream              i
                                                                                                     (6)
where m is mass flow. Air is considered to be 23.31
percent C>2 and 76.69 percent N2 by mass.  All the
mass flows of each species input into the unit are
summed and divided by the molecule weight (MW) of
that species to calculate molar flows (M) by equation
7:
                                          m.
                                                        Molar Flow. =
                                                                                                     (7)
Table  E-2  lists  the molecular weights  of  each
species.

Complete combustion is calculated according to the
molar  equations  listed  in Table E-3.  A  warning is
issued if insufficient oxygen is present for  complete
combustion  or if  insufficient hydrogen  is  present for
complete conversion of Cl to HCI.
where  Aj is the area of  each section  and Aj is the
total refractory area.
                        The volumetric flow is calculated  from the total  flow
                        by the ideal gas law in the form of equation 8:
                                                  127

-------
Volumetric Flow (@ 70°F)
^— sft (K)
= Y Molar Flow, x 386.7 	 W
*-~ i HJ mole i
/H2°f
-UcJ „
Dry oxygen volume percentage fs~ calculated from the x CAp 1.92 jj
molar flows by equation 9:
Dry 69 Volume Percentage Table E-2- Molecular Weights of Species Considered In
, Energy and Mass Balance
M : ..•••".•
0,, Species , Molecular Weight
	 xlOO% (9)
MC02 + MN2+VMS02
Finally, molar flows are converted back into mass
flows by equation 10:
m. = M.xMW. (10)
i ii
£.7.3 Energy Balance
The energy balance solves three equations: .
Heat of Combustion + Sensible Heat
- Heat of Vaporization - Total Radiation
- Total Convection = 0 (11)
Radiation to Refractory
+ Convection to Refractory Table E-3
- Conduction Through Refractory = 0 (12)
Conduction Through Refractory
- Radiation from Outer Shell
- Convection from Outer Shell = 0 (13)
for gas temperature, wall temperature, and outer shell
temperature.
The heat of combustion is the heat released in the
reaction of reactants to products at the reference
state of 77° F with H20 in liquid form. The heat of
combustion is calculated by equation 14:
Heat of Combustion = S [(HHVixmi)
-(Heat of Solution xClixm;)] (14)
where (H^C
where HHV is higher heating value and Heat of produced i
Solution is the energy released when gaseous HCI calculated b
dissolves in water. The heat of solution of HCI is
subtracted out because HHV is typically measured
with HCI in aqueous form, but the reference state of „
HCI used in the program is gaseous. The heat of ' ( '
C 12
H 1
N 14
O 16
S 32
Cl 35.5
Ash
H2O 18
Oz 32
N2 . ... 28
C02 44
HCI 36.5
S02 64
Molar Equations for Complete Combustion
C + O2 = CO2
H + i02 = }H26
N = JN2
O = }O2
S + 02 = SO2
Cl + H = HCI
H2O = H2O
Excess 02 = C>2
. N2 = N2
CO2 = CO2
HCI = HCI
)/HCI) is the molar ratio of H20 to HCI
n the oxidation of the fuel/waste as
y:
(*\ ( C1 V
j°\ Vl / V 35.57 (i6)
solution of HCI is based on a curve fit to data \HCl7 / Cl \
presented in Daniels and Alberty (1967) (1): 2x( 	 I
\ 35.5 /
Heat of Solution! Higher heating value is used because of the choice of
= m.X Cl. (1 - Moisture.)887.36
liquid water as  the reference state.  The heat  of
vaporization is the energy required to convert reactant
and  product water to  liquid  H2O  at the  reference
temperature of 77° F according to equation 17;
                                            128

-------
            vap   \  reactant steam    product steam

                        Btu
             X 1,050.54	
                         ID
 (17)
         where all product water is assumed to be in the form
         of steam. The change in sensible heat is the sensible
         heat of the products minus the  sensible heat of  the
         inputs.  Sensible  heats  are calculated  according  to
         equation 18:

            Sensible Heat. = m. C . (T - 77°F)         (18)
                         i     i  pi
         For input streams,  T is  the preheat temperature and
         Cp is the heat capacity which is  given for fuel/waste
         streams and is assumed to be 1.00, 0.44,  0.24, and
         0.22 Btu/lb°F for liquid water, steam, air, and oxygen,
         respectively. For products, T is the gas temperature,
         and  Cp is the mean heat capacity of each species
         between  the  reference temperature  and  the  gas
         temperature.  For  gas  species,  Cp is calculated
         according to equation 19:
                              ),(T2-T2ef
            pi
i.(T-T  ,)+•
 i     ref        2
             - (T-Tref)
                           +
                              l.(T4-T4
                                      ref
                                                  (19)
        with constants a, b, c, and d for species COa,  H20,
        N2, SC-2, HCI,  and C>2 taken from  Hougen, Watson
        and  Ragatz  (1967)  (2). For ash,  heat  capacity  is
        calculated from an integration of a formula from  Perry
        and Chilton (1973) according to equation 20(3):
                   0.18( T-T f j + 0.00003(T2-T2ef
           ^p ash
                                T-T
                                     ref
                                                       (20)
        Heat loss through the wall is calculated from the area
        (A), the conductivity and thickness of the refractory,
        and from the difference between the inside refractory
        wall temperature and the  outer shell temperature as
        shown in equation 21:

        Heat Loss Through Wall
I

                     T    —T
                     J.  -, —"• J. .  .,
                      wall    shell
                                   v
(21)
                                                             according to equation 22:
           Convection = hA  T   -T
                                    wall
                                                                                         (22)
         where h  is the corrective heat transfer coefficient
         and TCOO| can be  substituted for Twa|| for  heat
         transfer to cooled  surfaces.  The  heat  transfer
         coefficient is defined by equation 23:
                         K
                  = Nu
                          D
                                                     (23)
         where Kgas is the thermal conductivity of the gas, Nu
         is the Nusselt number, and D is the effective diameter
         of the incinerator. For noncylindrical  incinerators,  the
         effective diameter and length (L)  are calculated from
         the area and volume (V) by the simultaneous solution
         of equations 24 and 25:
                                                                 A =
                 2D2n
                        + DnL
                                                                      V =
                                                                           LD2n
                                                                                                          (24)
                                                      (25)
        Gas  thermal  conductivity  is  approximated by  a
        method taken  from Perry and  Ghilton (1973)  and
        tailored to combustion gases  according to  equation
        26 (3):
             K   =
                                                        0.3703u(c +0.0855

                                                           C   . + 0.0855
                                                             pref
                                                      (26)
        where Cp ref is the heat capacity of  the  gas at a
        reference temperature of  1,500°F and  p, is the
        viscosity of  the gas which  is approximated  by a
        method taken from  Perry and Chilton (1973)  and
        tailored to  combustion gases  according to  equation
        27(3):
                                                                        >-5
                         l,960°fl
                                                                                      1.5
                                                                          2,180.5°R

                                                                        (T + 220.5°R)
                                                     (27)
        The Nusselt  number  is  estimated  from  Kroll's
        correlation  for tubular combustors as referenced by
        Field, et al (1967) according to equation 28 (4):
                                             Nu = 0.023 Re°'8 Pr0'4
                                                                                            ,0.7
                                                                                                          (28)
        Heat loss through cooled surfaces is the sum of the
        convective  and radiative  heat transfer to those
        surfaces. Convective  heat transfer is calculated
        where Re  is the  Reynolds number and Pr is the
        Prandtl  number. The Prandtl number is defined by
        equation 29:
I
    129

-------
                                                     temperature:
      Pr=
                                             (29)
           K
             gas
and the Reynolds number is defined by equation 30:
        Re =
             PU°
                                             (30)
where  p is  the  gas density  which is  calculated  by
equation 31:
   p = MW
                   mole     530°R   sft
           mean  386,7 sft3
                                      sn_     (31)

                                      ft3
MWmean is the mean molecular weight of the gas as
calculated in equation 32:
    MW
                / m. —
                    l
                       m
                          ,
                                              (32)
        mean
and U is the gas velocity calculated from equation 33:



          (lmi-mash)                     (33)
   U = 4
               pD2n
Radiation  is the dominant mode of heat transfer at
typical  incineration  temperatures.  The general
equation for emitted radiation is:
      Radiation = eAoT4
                                            (34)
where  o is  the  Stefan-Boltzmann  constant. Emitted
radiation can come from the gas, in which case e is
the emissivity of the gas, A is the total area of the
incinerator unit, and T is the  gas  temperature; or it
can come from the refractory wall (cooled surfaces
are assumed to be too cold to  radiate significantly), in
which case  £ is the emissivity of the refractory, A is
the refractory area, and T  is  the  refractory wall
temperature.

Wall emissivity is assumed to be 0.8, typical of many
dirty refractories.  Gas  emissivity  is  calculated  by
Johnson's (1973) (5) gray gas  approach as described
by  Richter  (1981)  (6) where  the  emissivity  of the
absorbing gases is characterized as  the sum of the
emissivities of three weighted gray components:


   e  = £a. 1-expf-K.BLJ              (35)
              L       ^        » J
where BL is the mean beam length of the  incinerator
and  the  weighting  factor  a;  is a  function  of
                                                                           c.
                                                                 a. =b. + -
                                                                                                  (36)
                                                     The absorption  coefficient Kj is a function of the
                                                     partial  pressures of the  absorbing  gases  H20 and
                                                     C02:
                                                     where:
                                                                   M
                                                                     H2°
                                                                                                  (37)
                                                                                                  (38)
                                                     and
                                                                   M
                                                                     co
                                                           PC02 =
                                                                                                  (39)
                                                     Values of b,  c,  and d are tabulated  in  Table E-4.
                                                     The emissivity due to soot is calculated as described
                                                     by Sarofim (1978) (7):
                                                                                                  (40)
                                                     where FV is the volume of soot per volume of gas
                                                     and is calculated from:
                                                         FV =
                                                                                                  (41)
                                                                   J  / m.—
                                                                sooty 4-   i
                                                                            m
                                                                              ash
                                                     where Psoot >s assumed to be 2 g/cm3 and msoot is
                                                     assumed to be 2 percent of the volatile carbon.
                                                                                                 (42)
                                                        m    = 0.02 Y m.CxVol
                                                         soot        ^- \  i

                                                     The emissivity of the composite gas is:
                                                     BL is the mean beam length of the incinerator. The
                                                     mean beam length is approximated by a curve fit to
                                                     beam  lengths  of  a gas radiating to  cylinders  of
                                                     different dimensions:
                                                 130

-------
  BL = 0.30 + 0.65  l-exp(	:—J         (44)

The radiative heat  transfer  calculation  begins with
emissions from the gas.  The emitted radiation strikes
the walls. The proportion which strikes the refractory
wall is determined by the ratio of the  refractory area
to the total area with the  remainder  striking cooled
surfaces. The proportion of  the radiation  which is
absorbed  by the  wall  is  the  same as  the wall
emissivity,  assumed to be 0.8 for both refractory and
cooled surfaces,  the remainder being  reflected. The
reflected radiation,  along with radiation emitted from
the walls, passes through the gas.  The proportion of
the radiation  which  is absorbed by the  gas is the
same  as  the gas  emissivity  with  the remainder
passing  through  to  strike the far  wall.  Radiation is
followed  in this manner, reflecting and being absorbed
by  refractory  walls  and  cooled  surfaces and  being
transmitted through  and  being absorbed  by  the gas
until a negligible proportion  remains.  Radiative heat
transfer  from  each  element  (gas,  wall,  and cooled
surface)  is  determined by:
  Radiative Heat Transfer = Emission

            — ^T Absorption
   Table E-4.   Weighted Gray Gas Constants
    i        b        ; c, "R-i        d. (ft-atm)-i
(45)
1
2
3
0.13
0.595
0.275
0.000147
-0.0000833
-0.0000639
0
0.258
8.107
Heat  transfer from the outer  shell to the ambient
surroundings is the sum of the heat transfer due to
free  convection and  radiation.  Free  convection is
calculated from a correlation for free convection from
a horizontal cylinder taken from  McAdams (1953) (8):
   Free Convection = 0.18
Btu/hr

  °R
               ~ Tambient/   X Ashell
                                              (46)
        A  Newton  Raphson iterative  technique  is  used  to
        solve equations  11  and 12  for an  initial outer shell
        temperature guess.  Initial gas  and wall temperatures
        are  estimated,  and  the left-hand  sides  of the
        equations and their derivatives are solved.  Revised
        gas  and  wall  temperatures  are  estimated  from
        equations 47 and 48:
           T       = T
             gas new    gas old
                        8(11)
                        8T
                          wall
                                                            8(12)

                                                           8T
                                                        (47)
                                                              wall
                8(12)    8(11)
                     x
                8T
                  gas
                                           8T
                          wall
8(11)

8T
  gas
         8(12)

        8T   „
          wall
           T        = T
            wall new    wall old
                        8(12)         8(11)
                              -(12)x
                                                       (48)
                                                                      8T
                                      8T
                                   8(12)    8(11)
                                         x
               8T
                                                                gas
                                                                     8T
                                                                       wall
8(11)   8(12)

8T
                                                            8T
                                          wall
       The iterative process is continued until Tgas and Twa|l
       yield solutions to the left hand  sides of equations 11
       and 12 with absolute values less than 1/10,000 of the
       sensible heat in the unit. If the outer shell temperature
       is not given, the outer shell temperature estimate is
       revised, and  the  process  is  repeated  until  the
       absolute value of the left-hand  side of equation  13 is
       also  less than  1/10,000  of the sensible heat in the
       unit. At this point, the energy balance is complete.

       For fluidized-beds, heat transfer between the  gas and
       walls is  assumed to be  fast; thus, gas  temperature
       and wall temperature  are assumed to  be the same.
       Equations  11 and 12 are combined so that only two
       equations must be solved for Tgas and TShei|.

       £.7.4 Residence Time
       Mean residence time in a unit  is calculated from the
       temperature, volume, and volumetric flow of the unit:
               Volumetric Flow (@T  )
                                                                                     T   + 460°R
                                                                                                   (49)
          = Volumetric Flow (@ 70°F) x
                                      70°F
and radiation is calculated from equation 34 using 0.7
as the outer shell emissivity.
                                                                       Volume
                                                     (50)
                 Volumetric Flow I
                                                  131

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 £.1.5 Units In Series
 For units in series, the  products  of  complete
 combustion along with the  sensible heat they carry
 are passed from one unit to the next and are added
 to all the  new inputs to the next unit. If ash drops out
 of the first unit, its mass flow and  sensible heat are
 subtracted out and not passed to the second unit.

 £.1.6 APCE
 The APCE calculations in the current version of the
 energy and mass balance simply  determine the flow,
 acid loading, and quench  water  requirement of  the
 effluent passing  to  the  APCE.  Developments  are
 currently underway to allow more  detailed evaluations
 of  specific  equipment performance such  as ESPs,
 venturi scrubbers, packed tower,  cyclones, and  FFs.
 These will be incorporated  into the  software in future
 updates.

 Flow is calculated in terms of dry volumetric flow from
 the last unit at standard conditions:

  Dry Volumetric Flow (@ TOT)
Molar Flow. -M  _x 386.7
                2
                                        o
                                     sft
                        u _     .
                        H°       Ibmole/
Acid loading is simply the mass flow of HCI from the
last unit:
   Acid Loading = m
                                             (52)
                    HCI
Quench  water  requirement  is the amount of water
necessary to  quench  the effluent  from the  exit
temperature of the last  unit to the temperature at
which the gas  is saturated with  water. All cooling is
assumed  to  occur by evaporation  and  changes in
sensible heat.

First,  the saturation temperature is  estimated.  The
energy required to cool the  gas to the saturation
temperature is calculated:

Sensible Heat
        ,   t
      exhaust  p mean
           T      —T
             exhaust   saturated,
                                             (53)
where  the mean  heat  capacity is calculated  from
equations 19  and 20.  Then  the  amount  of  water
necessary to cool the exhaust gas is calculated:
                Sensible Heat
             rp        	m      1 ATT
      p water   saturated   watery   vap water
                                             (54)
The  water  content of the effluent is compared with
the vapor pressure curve of water to determine how
close the  effluent is to saturation.  The  saturation
                                            temperature estimate  is adjusted and  equations 53
                                            and  54  are  recalculated. This  iterative  process
                                            continues  until  the  effluent is within  0.5°F  of
                                            saturation.

                                            As the effluent cools from  the quenched temperature
                                            to the stack temperature, the vapor pressure of water
                                            decreases and the excess water  is assumed to drop
                                            out so that the effluent remains saturated. Thus, the
                                            total flow at the stack is calculated by .equation 55:
                                            Stack Volumetric Flow (@70°F)
                                                   Dry Volumetric Flow (@ 70°F)

                                                  1 a tin — Vapor Pressure of Water
                                                  (@ stack temperature)
                                             (55)
 £.7.7   Limitations of the Current Procedure
 The June  1987  version of  the  energy and mass
 balance procedure  is  subject to  the  following
 limitations:

 1.  It is only applicable  to  fuel-lean  incinerators.
    The  complete  combustion assumption is  no
    longer valid under fuel-rich situations.

 2.  It tends  to overpredict  temperatures in high-
    temperature,  nearly stoichiometric conditions
    where significant equilibrium concentrations of CO
    and OH exist.

 3.  It  is  not  applicable  to  cold-wall,  flame-
    dominated incinerators  where waste destruction
    may be  controlled  by  mixing  and  by flame
    temperature  which  is  very different from  exit
    temperature.

 4.  It is of limited value  for incinerators which cannot
    be  characterized by  a single mean  temperature,
    such as  a long  incinerator  with  a significant
    temperature profile.

5.  It does not account  for unquantified heat losses
    which are not evident  in the input data.  Heat
    losses from  often overlooked sources such  as
    water-cooled  burners and  probes,  view ports,
    gaps in the refractory, etc., may account for most
    of the heat loss in some  incinerators.  Thus,  the
    program  tends  to overpredict temperatures in
    incinerators with  significant,  unquantified heat
    losses.


 E.2 References
1.  Daniels, F. and  R.A.  Alberty. Physical Chemistry.
    New York: John Wiley and Sons.  1967, p. 53.

2.  Hougen,  O.A.,  K. Watson, and  R.A. Ragatz.
    Chemical Process Principles, Part I: Material and
                                                 132

-------
   Energy Balances. New York:   John Wiley and
   Sons.  1967.

3.  Perry,  R.H.  and  C.H.  Chilton.  Chemical
   Engineers'  Handbook • Fifth Edition.  New  York:
   McGraw-Hill.   1973.

4.  Field,' MA, D.W. Gill,  8.B. Morgan, and P.G.W.
   Hawksley.  Combustion  of  Pulverised  Coal.
   Leatherhead:   The  British  Coal  Utilisation
   Research Association. 1967, p.  119.

5.  Johnson, T.R. and J.M. Beer.  The Zone Method
   Analysis of Radiant Heat Transfer: A Model for
   Luminous Radiation.  J. Inst. Fuel. 46:388.  1973.
6.  Richter, W. Assessment of Pulverized Coal Fired
   Combustor Performance—Models  for  Coal
   Combustor Performance,  Analytical  Tool
   Verification.  Topical Report.  DOE Contract No.
   DE-AC-80PC30297.  1981.

7.  Sarofim, A.F. and H.C. Hottel. Radiative Transfer
   in Combustion Chambers:  Influence of Alternative
   Fuels.   Washington:   Hemisphere  Publishers/
   1978  pp.  199-217.

8.  McAdams,  W.H.  Heat Transmission.  New  York:
   McGraw-Hill.  1953, p. 177.
                                              133

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                                                    APPENDIX F
                                            Example Reporting Forms
        This appendix contains  copies  of  blank  forms that
        may be used  as  a format  guide to  summarize  the
        results  of  the trial  burn.  These  forms are only
        intended  to  summarize  certain,  fundamental,
        information in a format which will facilitate review of
        the report. They do not call for all of the  information
        which is needed in a full trial burn  report.  Because
        every incinerator  system is somewhat different,  in
        many cases additional information will be  necessary.
        Conversely,  some  of the  information  listed on  the
        forms may not be  needed for  the evaluation.  The
        applicant should, however,  be aware that using as
        consistent as possible a  format,  for summarizing  the
        trial burn results will make it easier for the  reviewer to
        evaluate  the  report and,  hence,  expedite  the
        permitting procedure.

        Table F-1  lists the  forms  and how they  are to  be
        used. The  forms  are grouped  into the following
        categories:

        1. Facility and  design information, Forms  1 and  2--
          This information should be included in the trial burn
          plan as well as in the report.
    2. Listing  of  the  target settings for the trial  burn,
      Forms  3,  4, 5,  and 6--This  information  can  be
      included in the trial burn plan as well as in the
      report.

    3. Summary of the system's operating conditions and
      performance during the trial burn, Forms 3, 4,  5, 6,
      7, 8, 9,  10 and 11--These forms can  be  used to
      summarize the  data for each run, they can also be
      used to  present a summary of the information  for
      each test of the trial burn. In this way, the reviewer
      can evaluate the summary of the results of the trial
      burn  and if additional information  on the runs  for
      that  test is desired, it is it can be found on the
      same form summarizing the results of each run.

    4. Recordkeeping,  Forms  10 and  12--These forms
      can  be  used to  keep the log of the monitoring
      parameters required by the permit during operation
      and during the trial burn, if needed.

    These  forms should be presented in the report  on
    only  one  side of  the  paper-no  two-sided  copies.
    This  allows the permit reviewer to spread them out
    and compare the entries.
I
135

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Table F-1.    Recommended Usage of Sample Forms In Trial Burn Report
       Form no.
                    Tide
Number of copies/Purpose
           1

           2

           3

           4

           5
           7

          8a

          8b

          9a


          9b

          9c


          10


          11

          12
Summary of Facility Information

Summary of Design Information

Description of Waste Streams

Summary of Test Conditions (Waste Feed)

Summary of Operating Parameter Values


Summary of System Performance


Method 5 and Paniculate Results

Input Rates

Chloride Emissions

POHC Emissions (May be used for volatiles and semivolatiles
or use Form 9c for semivolatiles separately.)

POHC Input Rates

Semivolatile POHC Emissions (May be used in lieu of Form 9a
for semivolatile emission results.)

Monitoring Data for Halides and Inorganic Ash
and Operations

List of Samples

Emergency Shutdown and Permit Compliance Record
          I/a

          I/a

          I/a

      1 per test/b*

       1 per test/b
       1 per run/c

       1 per test/b
       1 per run/c

       1 per run/c

       1 per run/c  -VM

       1 per run/c


       1 per run/c

       1 per run/c


       1 per run/c

       1 per run/c


       1 per test/d

    I/Operation only
   Note: Submit pages that have been copied on one side only to facilitate evaluation and review.

   a    To indicate the range of values that would be encountered during operation or to describe the facility.
   b    To summarize the results of each test, i.e., average of the runs for that test condition.
   c    To summarize the results of each run.  (The average of these data for each test constitute to input to "b,"
        above.)
   d    As a QA/QC check on the samples taken during the test.

   *If waste composition changes for each run then Form 3 should be included to identify the actual composition of the
   wastes burned during each run.
                                                    136

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          Form 1.  Summary of Facility Information
k
              EPA facility ID No.

              Facility name

              Contact Person

                      Telephone No.

                      Facility Address
                      FJ*A Region

              Person responsible for trial
                burn report

                      Telephone No.

                      Company name

                      Address
                      Date                                 -	

              Have proper QA/QC procedures
                been followed?                                  Yes	   No.

              Person responsible for QA/QC	

                      Title                                    .	__

                      Address                           ••  	•	
                      Telephone No.
137

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                Form 2. Summary of Design Information
                    Parameter                      Units
                    Incinerator ID
                    Installation date (year)
                    Type of incinerator
                                                                      PCC                SCC               System
                    Inside dimensions               	   	   	   	:-   ,_
                      (dia. x length or height x width x length)
                    Cross sectional area              	
                    Combustion chamber volume	
                    Design heat release rate          	
                    Refractory thickness^            	
                    Refractory conductivity*1         	
                    Refractory surface areaa          	
I                    Cooled surface area3             	
                    Design pressure                 	
                    ID fan capacity
                    Stack diameter
                    Stack height
                    APCE design information (as applicable)
                    Type(s) (quench, Venturi, ESP, etc.)
                    Maximum inlet temperature
                    Minimum inlet temperature
                    Maximum inlet pressure
                    Minimum inlet pressure
                    Design pressure drop (range)
                    Design liquid flow (range)
                    Design gas flow (range)
                    Surface area (bags, plates)
                    Voltage (specify AC/DC)
                    Current
                    HC1 removal capacity
                          Burner                                   Waste              Atomizing         Type atomizing
                       identificationb            Type              stream(s)          fluid pressures            fluid
                   aRequired for mass and energy balance,
                   bQnly need to identify burners used for waste.
                   cif different from design specifications, explain.
                                                                    138

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Form 3.  Description of Waste Streams
  Complete one of the following three columns:
  Expected operating conditions	              Run results                                     Test results, Test #.
                              (check)              	    Run number                         Average of runs
                                                 	 Date                                Nos.	• 	
                                                                                   Waste stream identifiers

  Parameter                      Units        	   	   	   	
  Type*
  Typeoffeedb
  Location of feed
  Nominal feed ratec
  Container size
  Container typed
  Container Frequency6
  Physical state
  HHV
  Density
  Viscosity
  Ultimate Analysis
      Water
      Ash
      Carbon!
      Hydrogen!
      Oxygen!
      Chlorine^
      Sulfur!
      Nitrogen!
                                                                    (continued)

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Form 3.  Description of Waste Streams (concluded)
                                                                                    Waste stream identifiers
 Parameter
Units
 Organic Constituents (list)f
  Metals and salts (list)
  $Only organic and acid or acid-forming compounds of these fed to incinerator.
  aHigh BTU liquid, aqueous waste, sludge, containerized solids, etc.
  bSteam atomizing nozzle, ram feed, etc.
  cLb/h, kg/h, etc.
  dpiber drum, steel dram, etc.
  &One container every 5 min.
  fIdentify POHC's with an .asterisk (*).

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Form 4.  Summary of Test Conditions-(Waste Feeds)
     Test No.	
             (if data for a run)
     Parameter
                 Data from each run or average for each test
                           (min. 3 runs = 1 test)
Units
     Test Dates
     Elapsed time average

     Feed rate of each waste burned

        1.	
           Size of containers
           Maximum
           Minimum
           Mean

        2.	
           Size of containers
           Maximum
           Minimum
           Mean

        3.	
           Size of containers
           Maximum
           Minimum
           Mean

        4.        	
           Size of containers
           Maximum
           Minimum
           Mean

        5.	_____
           Size of containers
           Maximum
           Minimum
           Mean
     Total (mean) feed rate of all wastes to PCC
     Total (mean) feed rate of all wastes to SCC
     Auxiliary fuel used (total)
        Fuel
        Fuel	
        Fuel	
                                                 (continued)
                                                   141

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Form 4.  Summary of Test Conditions (Waste Feeds) (concluded)
     Test No.	                                    Data from each run or average for each test
             (if data for a run)                                             (tnin. 3 runs = 1 test)
     Parameter                            Units     	   		
        Metals and salts
        Organic Chloride

        Other materials of concern
                                                     142

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Form 5. Summary of Operating Parameter Values
    Test No.	                                 Data from each run or average for each test
            (if data for a run)                                         (min. 3 runs = 1 test)
    Parameter                         Units    	   	  	   	
    PCC temperature
       Maximum
       Minimum
       Mean

    SCC temperature
       Maximum
       Minimum
       Mean
    Combustion gas flowrate (identify on P&I or schematic where measured)
       Actual T =	,P =	
       Maximum                      	   	   	
       Minimum                      	   	   	
       Mean                         	   	   	
       @STP   T =	,P = .
       Maximum
       Minimum
       Mean

    Waste feed pressure
    Atomizing fluid pressure
    Combustion air blower power
    ID fan power

    PCC pressure
       Maximum
       Minimum
       Mean

    SCC pressure
       Maximum
       Minimum
       Mean

    APCE operating conditions
    Quench
       Inlet temperature mean
       Outlet temperature mean
       Water feed rate
          Maximum
          Minimum
          Mean
                                               (continued)
                                                 143

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Form 5. Summary of Operating Parameter Values (concluded)
     Test No.	                                Data from each ran or average for each test
             (if data for a ran)                                         (min. 3 runs = 1 test)
     Parameter                          Units     	  	   	   	
     APCE (as applicable)
        Water/liquor flowrate
           Maximum
           Minimum
           Mean
        Inlet temperature mean
        Exit temperature mean
        Pressure drop
           Maximum
           Minimum
           Mean

        L/G ratio
           Maximum
           Minimum
           Mean

        Influent pH
           Maximum
           Minimum
           Mean

        Effluent pH
           Maximum
           Minimum
           Mean

     Scrubbant blowdown rate

        Nozzle pressure
           Maximum
           Minimum
           Mean

        Plate voltage
           Maximum
           Minimum
           Mean

        Current
           Maximum
           Minimum
           Mean

        Sparking rate mean
                                                 144

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Form 6.  Summary of System Performance
    Test No.	                                  Data from each run or average for each test
            (if data for a ran)                                           (min. 3 runs = 1 tCSt)
    Parameter                           Units     	   	   	    	
    Performance
    Flue gas
       Flowrate (actual), mean

       Flowrate (STP), mean
       Velocity (actual), mean

       Velocity (STP) mean

    Flue gas composition (by volume)
       H2O
       O2 (by volume, dry)
       N2 (by volume, dry)
       CO2 (by volume, dry)
       CO (by volume, dry)
       Total unburned hydrocarbons
       SOX
       NOX
    CO (corrected to 7% O2)
          Maximum
          Minimum
          Mean

    Paniculate emissions
       Actual emission rate
       Actual concentration
       % Isokinetic
       Concentration corrected to 7% O2
       Metal	
       Metal	
       Metal	
       Metal	
       Emission rate
       IntoAPCE
       Out from APCE
       % removal
                                                (continued)
                                                   145

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Form 6. Summary of System Performance (concluded)
    Test No.	
            (if data for a ran)
    Parameter
Units
                Data from each run or average for each test
                          (min. 3 runs = 1. test)
    HCL
       Emission rate
       Into APCE
       Out from APCE
       % removal

    POHC input
    POHC emissions
    DRE for POHC
                                                  146

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Form 7.  Method S and Particulate Results3
                                                                                         Test or Run No.
                          Parameter
Units*
                  Sample time

                  Sample volume0

                  Stack gas volumetric flowrate

                  Stack gas volumetric flowrate0

                  Stack gas temperature

                  Stack gas moisture

                  Oxygen concentration0

                  Carbon dioxide concentration0

                  Percent isokinetic

                  Particulate collected

                  Paniculate concentration

                  Particulate concentration corrected
                      to 7% oxygen
% vol.
                  a Either metric or English units are acceptable as long as consistency is maintained throughout the report
                  b Dry standard basis.
                  c From Orsat analysis.

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                Form 8a. Chlorine Input Rates
                                                   Test or ran no.
                                                                                                     Test or run no.
Test or run no.


Waste/fuel stream

Feedrate
(kgAnin)
Chlorine
concentration
(%)
Chlorine
input rate
(gAnin)

Feedrate
(kgAnin)
Chlorine
Concentration
(*)
Chlorine
input rate
(gAnin)

Feedrate
(kgAnin)
Chlorine
concentration
(ft)
Chlorine
input rate
(gAnin)
•tx
00
                         Total

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             Form 8b. HCI Emissions3.1* and Removal Efficiency
                          Sample      Sample                                   HCI         Stack gas      Cl* emission      HCI emission    HCI removal
              Run No.      period      volume^         HCI collected*!       concentratione     flowratef          rate             rateg       effciency(%)
CO
              Blank value
              a Either metric or English units are acceptable as long as consistency is maintained throughout (he report.
              b This table is formatted to use chloride results from a single MM5 train (only one chloride emission sample is required per run).  If two MM5 trains are run,
                both sets of HCI data should be reported.
              c Sample volume is dry standard liters of stack gas.
              d Show value corrected for blank in parentheses.
              e Blank corrected as applicable.
              f Stack gas flow rate is dry normal (standard) m3/min.
              g Chloride emissions (lb/h) x 1.03.

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             Form 9a. POHC Emissions
Run No.
Trap pair
(for VOST)
Sample
period
Sample

(

Mass of each POHC collected

V> ( V> ( )»


( V» ( *« (


V»

                       Total/average*1
              POHC concentration (
              Stack gas flow rate (
              Emission rate (
Oi
O
         Total/averaged

POHC concentration (
Stack gas flow rate (
Emission rate (
                                              Jb
                                             )b
Average blank valued (
Standard deviationd (
Range of blank values^ (_
                                              )b
               Note:   This format is structured for VOST results. It may be used for MM5, a similar format would be used for integrated bag sampling for volatiles. Guidance for blank correction is provided in the
                      "Practical Guide—Trial Bums for Hazardous Waste Incinerators," Final Report, EPA-600/2-86-050,1986.
               Note:   Use parentheses to present results if two collectors are used in series (i.e., dual adsoprtion tubes on VOST).
                  a Either metric or English units are acceptable as long as consistency is maintained throughout the report.
                  b Sample volume is dry standard liters of stack gas.           d totals for sample period, volume, and amount collected; averages for concentration, flowrate, and emissions rate.
                  c Stack gas flowrate is dry nornial (standard) m^Anin.        e Indicate whether all (both field blanks and trip blanks) are used or whether only field blanks are used.

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Form 9b. POHC Input Rate, [Test Run] No.	
       Waste/Fuel stream
Waste feedrateb
   (kg/min)a
                                                                      POHC concentration0 (%)a/feedrate (g/min)a
ORE
                                                   d
                                                   e
                                                   d
                                                   e

                                                   d
                                                   e
                                                   d
                                                   e

                                                   d
                                                   e
                                                   d
                                                   e
  Total POHC feedrate
                                                   d
                                                   e
  a  Give units.
  b  Give feedrate measured during this run/test.
  c  Give concentration measured from sample taken during this test/run.
  d  Give concentration at POHC in each waste.
  e  Give feedrate of each POHC.

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            Form 9c. Semivolatile POHC Emissions3
              Run No.
             Sample
             period
                                      Sample
                                     volumeb
                                                 POHC collected
SV POHC No. 1       SV POHC No. 2
        POHC concentration
SV POHC No. 1    SV POHC No. 2
Stack gas        	Emission rate	
flowratec      SV POHC No. 1    SV POHC No. 2
CD
ho
Average blank value

Standard deviation

Range of blank values
             a Eilher metric or English units are acceptable as long as consistency is maintained throughout the report
             b Sample volume is diy at standard conditions (specify),
             c Slack gas flowrate is dry al standard conditions (specify).
             NOTE: This form may be used in lieu of Form 9b for summarizing emission results for semivolatile compounds.

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&
Form 10. Monitoring Data for Halides and Inorganic Ash Inputs
 Run/Test No.
Part A. Waste analysi
     Waste name
 Pumpable wastes
 PL
 P2.
 P3.
  Containerized wastes
  Cl. _
  C2. _
  C3. _ _
Sample ID no(s).c
                                                                  Maximum halides input rate =
                                                             Maximum inorganic ash input rate =
Total halides (%)
  (F, Cl,Br, I)
                                                                                                         Inorganic
                                                                                                         ash(%)
                                                                                                                    Specific gravity
                                                                  (continued)

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           Form 10. Monitoring Data for Halides and Inorganic Ash Input9
01
PaitB. Calculation of input rates
Pumpable wastes Containerized wastes
Time period
0000-0400
0400-0800
0800-1200
1200-1600
1600-2000
2000-2400
Waste Avg. flowrate Mass feed
No. for period rate
PI
P2
P3
Total for pumpable wastes
PI
P2
P3
Total for pumpable wastes
PI
P2
P3
Total for pumpable wastes
PI
P2
P3
Total for pumpable wastes
Pi
P2
P3
Total for pumpable wastes
PI
P2
P3
Total for pumpable wastes
No.
Halide input Ash input Waste containers Total mass
rate rate No. charged charged
Cl
C2
C3
Total for containerized wastes
Cl
C2
C3
Total for containerized wastes
Cl
C2
C3
Total for containerized wastes
Cl
C2
C3
Total for containerized wastes
Cl
C2
C3
Toial for containerized wastes
Cl
C2
C3
Total for containerized wastes

Total Total
Mass feed Halide input Ash input Halide input Ash input
rate rate rate rate rate

_ _
_ _


_ —
_ —


_ _
_ _


_ _
_ _


- _
_ _


_ _
- _


                                                                              (continued)

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CJ1
            Form 10. Monitoring Data for Halides and Inorganic Ash Input3 (concluded)
            Equations:**


                    Pumpable waste average flowrate (L/min)   =  Time-weighted average from continuously monitoring data logger

                                                      or
                                                                    Volume at end of period (L) - volume at beginning of period (L)
                                                                                                 240 min
                    Pumpable waste mass feed rate   =  average flowrate  (L/min) x specific gravity (kg/L) x 60 min/h


                                                                   n
                    Containerized waste total mass charged (KG)  = £ Gross weight (kg) - container tare weight (kg)
en                                                            where n =  number of containers charged during 4-h period
                                                         Total mass charged (kg)
                    Containerized mass feed rate   =  	
                                                                   4h
                                                 % Halide/ash
                    Halide/ash input rate  =  	x Mass feed rate
                                                       100
            a Either metric or English units are acceptable as long as consistency is maintained throughout the report.
            " Begin new form for each new set of analysis results.
            c If more than one sample is involved, list sample numbers and provide average results.
            d For clarity metric units are shown; English units can be used if desired as long as consistency is maintained throughout the report.

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             Form 11. List of Samples
             Test No.          Run No.      Type sample        ID no.        Date taken     Date analyzed      Notesa
CJl
01
             ^Note any problems, i.e., broken sample (by whom or where), damaged samples, questionable data, problems with analytical equipment, etc.

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              Form 12. Emergency Shutdown and Permit Compliance Record
              Facility ID No._
              Month                       Year
                                                                                 Automatic shutdown—check (V)
                                                                             	as appropriate	                                                         Regulatoiy
                Permit                                      Minimum/maximum  PCC waste  SCC waste                Time(min)                                              authorities
              exceedence                                     value recorded    automatic   automatic   Thermal relief     waste      Check (V) if                                  notified
                 No.     Date Time   Description of problem      (worst case)      shutdown   shutdown    vent opened3     shut-off    no shutdown^   Description of corrective action    (yes/no)
                  1

                  2

                  3

^                4
cn
•*                5

                  6

                  7
                  9

                  10
              a This example form describes the information generally needed for an emergency shutdown and permit compliance record. However, more space should be provided in actual forms if
                needed for adequate descriptions of problems and corrective actions.
              b Exceedance based upon facility operational records (no automatic waste shutdown triggered); corrective actions to address any malfunction of automatic waste feed shutoff system
                should also be described)

-------
             APPENDIX G

       Example Reporting Forms
Filled Out for Data from Example Problem
      General Facility Information
                159

-------
Form 1.  Summary of Facility Information
    EPA facility ID No.

    Facility name

    Contact Person

           Telephone No.

           Facility Address
                                         12345G739
XYZ  Chemical  Company
John F. Smith
(111)  555-5555
13  Pumpkin Lane
                                         Smith  City, ST  12345
           EPA Region

    Person responsible for trial
     burn report

           Telephone No.

           Company name

           Address
                                         XI
John  F.  Smith
see  above
see  above
           Date

    Have proper QA/QC procedures
     been followed?

    Person responsible for QA/QC

           Title

           Address
           Telephone No.
                                         June  13,  1988
     Yes   XX
Mary  Jane Doe
No
Quality Assurance Manager
Chemical  Laboratory Consultants

1313  Gourd Street	

Juice  City, ST   54321	

(111)  555-6666	
                                             160

-------
Form 2. Summary of Design Information
   Parameter
         Units
   Incinerator ID
   Installation date (year)
   Type of incinerator
                       Rotarv  Kiln  or RKI
                       1981
                       Rotar   Kiln  with  STH
m         _iy_
10°  kJ/h  72
                                cm
                                m
Inside dimensions              m  x m
  (dia. x length-wherghr/x-width-x-iength)
Cross sectional area
Combustion chamber volume
Design heat release rate
Refractory thickness^
Refractory conductivity^
Refractory surface area3
Cooled surface areaa
Design pressure
ID fan capacity
Stack diameter /area
Stack height

APCE design information (as applicable)
Type(s) (quench, Venturi, ESP, etc.)
Maximum inlet temperature
Minimum inlet temperature
Maximum inlet pressure
Minimum inlet pressure
Design pressure drop (range)
Design liquid flow (range)
Design gas flow (range)
Surface area (bags, plates)
Voltage (specify AC/DC)
Current
HC1 removal capacity
                                                 PCC
                                           3.4  x 6.7
                                           8.8
                                            sec
                                       3.G x 7.5
                                       10.3
                                                              36
                    15
                              15
                              kj/stn- c   n.nni44
                                kV
                    88
                              106
                                           0
                                       0
                                           slightly neg.    slightly neg,
                                                     System
                                                          108
                                                                                 570
                                                                                 0.61/1.17
                                                                                4&^3-
                                             3-stage wet ionizing scrubber
                                             N/A-gas     4-water
                                             N/A
                                             NA
N/A
1 /mi' n
m /mi n
400-80n
4on_Rnn

                      30
                                             variable,  dependent  on loading
                                             unknown—to be  determined  by test
     Burner
  identificationb

B-l	
B-2  a,b,c
                            Type
Air  atomiz.
Air  atomiz.
                       Waste
                      stream(s)
                                          <;i
          L1-L5 in  PCC
          L2-L5 in  SCC
                               Atomizing
                             fluid pressures
                                                              '
                                                           20-50  psi
                                                         20-50 psi
                                                                             Type atomizing
                                                                                 fluid
                                                                              -N
                                                                                 /fl
                                                                               Air
                                                                               Air
   ^Required for mass and energy balance.
   b(Dnly need to identify burners used for waste.
   cif different from design specifications, explain.
                                                161

-------
           Form 3. Description of Waste Streams
O)
10
Complete one of the following three columns:
Expected operating conditions XX
(check)
Parameter
Typea
Typeoffeedb
Location of feed
Nominal feed ratec
Container size
Container typed
Container Frequency6
Physical state
HHV
Density
Viscosity
Ultimate Analysis
Water
Ash (wet basis)
Carbon:}: (wet basis)
Hydrogen:}: (wet basis)
Oxygen:}: (wet uasis)
Chlorine:}: (wet basis)
Sulfur! (wet basis)
Nitrogen^ (wet L>as i s )
Units
kq/min
gal 	
min

kJ/kg

% wt
% wt
% wt
% wt
°L wt
% wt.
% wt.
% wt.
Run results
Run number
Date

SI

solids
drum
PCC
18.6
SS
steel drum
1/6 min
solid
20,900


4
45
36
q
3.8
7.7




S2

solids
bulk
PCC
8.4



solid
20,600


20
39
28
11
7





Testn
Avera
Nos.

esults,Test#
ige of runs

Waste stream identifiers
LI L2 L3

Lo Btu liq
nozzle
PCC/SCC
31



liquid
nil


98.67
0.07
0.05
0.01
1
0.?




Hi Btu liq
nozzle
PCC/SCC
2



liquid
32,700


15
1
50
16
3
15




Hi Btu liq
nozzle
PCC/SCC
0.4



liquid
35,460


2
2
78
in
8







L4

Hi Btu Liq
nozzle
PCC/SCC
6



liquid
31,500


2
0.8
52.2
15
4
?fi





L5

Hi Btu Liq
nozzle
PCC/SCC
0.4



liquid
34,600


10
3
48
?n
14
5





                                                                                (continued)

-------
IP
                Form 3.  Description of Waste Streams (concluded)
Parameter

Organic Constituents (list)f
Carbon
tetrachloricie
Trichloro-
ethylene*
Toluene
Chloroform
Perrhlorn-
et.hylenp*
R-Kt/'-rhlnrn)-
ethvlether
Tri <~hl nyn-
|->pr|7prip*
Phenol




Metals and salts (list)




Waste stream identifiers
Units SI S2 LI L2 L3 L4 L5


% wt (wet) 1.1 	 	 6.8 	 1R

°L wt (wet) l.fi - - - -- — 	 fi
% wt (wet.) 	 . n.i n_n? 	 ifi 	
°L wt (wet) 	 - — n Id 	 	 	 _

°L wt (wet) 	 	 	 	 in 	 	 	 ,._

% wt (we1") - — 	 	 	 — - l

% wt (wet) — 	 -- — 	 	 "5
% wt (wet) 	 	 - - 	 26 	









                 $OnIy organic and acid or acid-forming compounds of these fed to incinerator.
                 aHigh BTU liquid, aqueous waste, sludge, containerized solids, etc.
                 bSteam atomizing nozzle, ram feed, etc.
                 CLb/h, kg/h, etc.
                 dfiber drum, steel drum, etc.
                 eQne container every 5 min.
                 fldentify POHC's with an asterisk (*).

-------
             Form 3.  Description of Waste Streams
                                                                  Form 3. Description of Waste Streams
             Complete one of the following three columns:
             Expected operating conditions   XA               RUn results
                                         (check)             	
                          . Run number
                           Date
Test results, Test #.
Average of runs
Nos.	  	
en
             Parameter
                                                                                             Waste stream identifiers
Units
                                                          SL

Type*
Typeoffeedb
Location of feed
Nominal feed ratec
Container size
Container typed
Container Frequency6
Physical state
HHV
Density
Viscosity
Ultimate Analysis
Water
Ash
Carbon:}:
Hydrogen:):
Oxygen}
Chlorine}
Sulfur!
Nitrogen}
kg/mi n
oal



kJ/ka

% wt
% wt
% wt
% wt
% wt
% wt



sludge
Lance

y
	 _
	
	
sludge
6.200
_ _-
__...._
70
14
10
3
2.99
0.01



                                                                              (continued)

-------
             Form 3. Description of Waste Streams (concluded)
                                                                                                                                  Waste stream identifiers
            Parameter
                               Units
en
in
             Organic Constituents (list)f
                 Chlorobenzene         %  wt  (wet)  0.03
Metals and salts (list)
             $Only organic and acid or acid-forming compounds of these fed to incinerator.
             aHigh BTU liquid, aqueous waste, sludge, containerized solids, etc.
             bSteam atomizing nozzle, ram feed, etc.
             cLb/h, kg/h, etc.
             dpiber drum, steel drum, etc.
             eQne container every 5 min.
             fldentify POHCs with an asterisk (*).

-------
rr
                Form 4.  Summary of Test Conditions (Waste Feeds)
                   Test No. target
                          (if data for a run)
                   Parameter
                  Data from each run or average for each test
                           (min. 3 runs = 1 test)
  Units   Tests  1,2.3 	  	   	
                   Test Dates
                   Elapsed time average

                   Feed rate of each waste burned

                      l.  SI (drummed  waste)
                         Size of containers
                         Maximum
                         Minimum
                         Mean

                      2.  SI  (Ondgp)	
                         Size of containers
                         Maximum
                         Minimum
                         Mean

                      3.  LI (aqueou?)	
                         Size of containers
                         Maximum
                         Minimum
                         Mean (PCC)

                      4.  L2 (Hi Btu)	
                         Size of containers
                         Maximum
                         Minimum
                         Mean (SCC)

                      5.  L$ (Hi Btu)	
                         Size of containers
                         Maximum
                         Minimum
                         Mean
           N/A
 55 gal  dDjm_
                   Total (mean) feed rate of all wastes to PCC
                                                  kg/mln
                   Total (mean) feed rate of all wastes to SCC
                                                  kg/mi n
                   Auxiliary fuel used (total)
                     Fuel	
                     Fuel	
                     Fuel	
 kg/mi'n    ?7
 kg/min   JL
kg/min    31
kg/min    2.3
kg/mi n    6
          JZS_
a<; needed  to maintain  temperatures
                                                            (continued)
                                                               166

-------
Form 4.  Summary of Test Conditions (Waste Feeds) (concluded)
   Test No.  target                                     Data from each run or average for each test
           (if data for a nm)                                           (min. 3 runs = 1 test)
   Parameter                           Units   IPS t.s  1 .9,3 	   	    	
      Metals and salts
      Organic Chloride                 S/"11'"     2»650
      Other materials of concern
       Nnnp	
                                                   167

-------
Form 5. Summary of Operating Parameter Values
    Test No. target
           .(if data for a run)
    Parameter
                          Data from each run or average for each test
                                   (min. 3 runs = 1 test)
          Units   Tests  1.2,3	   	    	
    PCC temperature
       Maximum
       Minimum
       Mean

    SCC temperature
       Maximum
       Minimum
       Mean
                   900
                   i .nnn
    Combustion gas flowrate (identify on P&I or schematic where measured)
       Actual  T= ftnrr    .P=  1  atm
       Maximum                     	   	   	
       Minimum                       	   	   	
       Mean                         m /min
       @STP   T=
       Maximum
       Minimum
       Mean
    Waste feed pressure
    Atomizing fluid pressure
    Combustion air blower power
    ID fan power

    PCC pressure
      Maximum
      Minimum
      Mean

    SCC pressure
      Maximum
      Minimum
      Mean

    APCB operating conditions
    Quench
      Inlet temperature mean
      Outlet temperature mean
      Water feed rate
         Maximum
         Minimum
         Mean
.P= 1  a tin
        *C
        m  /min    500
                   N/A
                   N/A
                   N/A
                  -80
        L/rmn    UOTT
                                              (continued)
                                                168

-------
Form 5. Summary of Operating Parameter Values (concluded)
   Test No.  target
          (if data for a run)
   Parameter
 Units
                 Data from each run or average for each test
                          (min. 3 runs = 1 test)
   APCE (as applicable)
      Water/liquor flowrate
         Maximum
         Minimum
         Mean
      Inlet temperature mean
      Exit temperature mean
      Pressure drop
         Maximum
         Minimum
         Mean

      L/G ratio
         Maximum
         Minimum
         Mean

      Influent pH
         Maximum
         Minimum
         Mean

      EffluentpH
         Maximum
         Minimum
         Mean

   Scrubbant blowdown rate

      Nozzle pressure
         Maximum
         Minimum
         Mean

      Plate voltage
         Maximum
         Minimum
         Mean

      Current
         Maximum
         Minimum
         Mean

      Sparking rate mean
           Stage  1    Stage 2     Stage 3     Total APCE
I /min
Idfi
Tb
                      .2
             .2
L/min
          N/A
                                      -161-
                                               -80-
                                                N/A
                                                7.0
                                                N/A
                         15
                                               N/A
                                               30
                                                169

-------
Form 6. Summary of System Performance
   Test No.    t.argpt
           (if data for 8 run)
   Parameter
 Units
                  Data from each run or average for each test
                           (min. 3 runs = 1 test)

Performance
Flue gas
Flowrate (actual), mean
Flowrate (STP), mean
Velocity (actual), mean
Velocity (STP) mean
•3
HI /min 614 614
m3/min 510 510


RgQ
490


   Flue gas composition (by volume)
      H2O
      O2 (by volume, dry)
      N2 (by volume, dry)
      CO2 (by volume, dry)
      CO (by volume, dry)
      Total unbumed hydrocarbons
      SOX
      NOX
ta b lished— by
                                             cnndi'f"l'np(;
   CO (corrected to 1% O2)
         Maximum
         Minimum
         Mean

   Paniculate emissions
      Actual emission rate
      Actual concentration
      % Isokinetic
      Concentration corrected to 1% O2
      Metal	
      Metal	
      Metal	
      Metal	•
      Emission rate
      Into APCE
      Out from APCE
      % removal
ppm
    <100
<100
<100
To  be measured.
                                              (continued)
                                                 170

-------
        Form 6.  Summary of System Performance (concluded)
           Test No.  target
                  (if data for a run)
           Parameter
                Data from each run or average for each test
                        (min. 3 runs = 1 test)
 Units   Tests 1,2,3 	   	   	
           HCL
              Emission rate
              IntoAPCE
              Out from APCE
              % removal

           POHC input
               tn'chloroethylene
               perchloroethvlene
               trichlorobenzene
To be  measured.
          353
/mm
/min    	
/min     835
          220
           POHC emissions
                                         To  be measured.
           ORE for POHC
                                                   Tn
k
           171

-------
            Summary of Results of Tests 1,2, and 3
(Results of each test are means of the results of the three runs for that test.)
                                  172

-------
            Form 3. Description of Waste Streams
CJ
Complete one of the followin
Expected operating condition
Parameter
Type*
Typeoffeedb
Location of feed
Nominal feed rateC
Container size
Container typed
Container Frequency^
Physical state
HHV
Density
Viscosity
Ultimate Analysis
Water
Ash
Carbon!
Hydrogen!
Oxygen$
Chlorine!
Sulfur^
Nitrogen!
ig three columns:
IS
(check)
Units
kq/min






% wt
% wt
% wt
% wt
% wt
% wt
% wt
% wt

Run results


SI

solids
drum
PCC
27
55 qal.
steel drum
I/minutes



4
45
36
9
3.8
2.2





Run number
Date
SL

sludqe
lance
PCC
9
N/A






70
14
10
3
2.99
0.01






Test i
Aven
Nos. .
esults. Test #1,2,3
igeof runs
1 2 3

Waste stream identifiers
LI L2 L4

water
nozzle
PCC
30
N/A






98.67
0.07
0.05
0.01
1
0.2






Hi Btu lid)
nozzle
PCC
2.3
N/A






15
1
50
16
3
15






Hi Btu liq
nozzle
sec
6
N/A






2
0.8
52.2
15
4
26







                                                                                 (continued)

-------

























__
o

u
7T
£
s
w
o
Form 3. Description of Wast



^
0 ^
•a
c
g
Crt
Jj


—





t/






^


a
'S
>-)



Parameter





































































Organic Constituents (list/
Carbon-



CO
'-'


00
VD
















•-
4->
0)

4J
3
S3



tetrachloride


































Trirhloro-




*-°


















10

i — i

O
1
1
1
1
1





OJ
o
0













0)

4J
2
&S



OJ
cu
-3
h-










^
i — 1
O













OJ
2

4->
2
&s



Chloroform


































Perchloro-







O
i — i

















0)

.(_>
2
6-S



ethvlene*


































0
0
^=
o
OJ
to
•I—
CO




1 — 1










1
1
1
1







tu

4J
3
&«



ethvlether


































i
o
o
u
•r—
S-
h-




LO





















4J
Ol
2

+j
2
s«



benzene*


























Ol

4J
2
&«



Phenol










;
i
1



ro
O
O







4J
Ol
2

4J
2
5«



Chlorobenzene











































































































































Metals and salts (list)






















































































































tH
§
TO
fe
.S
•S .
2 ^
S «"
**H *O
O UH
*i3 *rt

o .9
1! :

u So
e5^ H
'g "w °. *^
to M
& •#
- •* e S
•« S S . «
tOnly organic and acid or a<
aHigh BTU liquid, aqueous
bSteam atomizing nozzle, ra
CLb/h, kg/h, etc.
dpiber drum, steel drum, etc
eOne container every 5 min.
fidentify POHC's with an as
174

-------
Form 4. Summary of Test Conditions (Waste Feeds)
    Test No. summary of  test results
           (if data for a run)
    Parameter                        Units
                 Data from each run or average for each test
                         (min. 3 runs = 1 test)
         Test 1      Test  2     Test 3     	
    Test Dates
    Elapsed time average

    Feed rate of each waste burned

       l.  SI drummed	
         Size of containers
         Maximum
         Minimum
         Mean

       2.  SL sludge	
         Size of containers
         Maximum
         Minimum
         Mean
         5/1?-13/87  5/13-14/87 5/15-16/87
kg/mi n  277D~
kg/min  S7T
      3-  LI aqueous
         Size of containers
         Maximum
         Minimum
         Mean

      4-  12 Hi  Btu liq  (PCC)
         Size of containers
         Maximum
         Minimum
         Mean

      5.  14 Hi  Btu liq  (SCC)
         Size of containers
         Maximum
         Minimum
         Mean
kg/min  30.0
kg/min  2.2
kg/min   5.9
   Total (mean) feed rate of all wastes to PCC
                                   kg/min   72.6
   Total (mean) feed rate of all wastes to SCC
                                   kg/min   5.9
                     120
7TF"
27T
6.0
                      73.2
                      6.0
   Auxilliary fuel used (total) (mean per run  for each  test)
      Fuel natural  gas	      kg/min   5.71         5.65
      Fuel	      	   	   	
      Fuel
             120
             'd/.O
T7b
             ?ft ft
~6TO~
             69.0
             6.0
                                  5.60
                                            (continued)
                                               175

-------
Form 4. Summary of Test Conditions (Waste Feeds) (concluded)
    Test No.  summary of  test results
            (if data for a run)
    Parameter                          Units
                  Data from each run or average for each test
                            (min. 3 runs = 1 test)
          Test 1       Tpst. ?      Tpst.  3      	
       Metals and salts
       Organic Chloride

       Other materials of concern
g/min
                                                   176

-------
Form 5.  Summary of Operating Parameter Values
Test No. summary of test results Data from each run or average for each test
(if data for a run) (min. 3 runs = 1 test)
Parameter Units Test 1 Test 2 Test 3

PCC temperature
Maximum
Minimum
Mean
SCC temperature
Maximum
Minimum
Mean
Combustion gas flowrate (identify on
Actual T = 7] -P= J.
Maximum
Minimum
Mean
(S>STP T= 20*C .P =
Maximum
Minimum
Mean
Waste feed pressure
Atomizing fluid pressure
Combustion air blower power
ID fan power
PCC pressure
Maximum
Minimum
Mean
SCC pressure
Maximum
Minimum
Mean
APCE operating conditions
Quench
Inlet temperature mean
Outlet temperature mean
Water feed rate
Maximum
Minimum
Mean

*C 916
'C 910
•C 914
T. 1 304q

r i arun

821
804
814
i jOin
QR4
qR?

804
733
fiOO
Q71
qR4
qtiR
P&I or schematic where measured)
atia
m /min 8Q2
m /min 8^0
m /min RfiK
1 atm
m /min 515
m.r/min 481
m /min 501

Dsi "3Q
|J J 1 U
N/A

mm H-,0 -l.fi
MUM •"2': * • •
mrri H->0 -7.7
2
mm H_0 -7.fi
/_'
mm H/jO -R.fi
mm H ^0 -8.?
2
•r
1 OdO
^ 78
965
852
L/min 910
892
830
Sfifi
518
496
508
-IP measured,
30
N/A

-2 n
-? n
-?.n
-R.q
-R q.1
-R.q
032
80
927
840
886
8^8
813
097
4Q8
484
4Q2

30
N/A

-2 fi
-? n
-9 4
-R.I
-R.fi
-R 4
Q58
79
958
8/1
91b
                                                  (continued)
                                                     177

-------
Form 5.  Summary of Operating Parameter Values (concluded)
    TestNo.  summary Of  test results              Data from each run or average for each test
           (if data for a ran)                                       (min. 3 TUHS = 1 test)
    Parameter    ,                    Units    Jest  I      Jest 2      Jest  ?       ••  -
    APCE (as applicable)
      Water/liquor flowrate
         Maximum
         Minimum
      Nozzle pressure
         Maximum
         Minimum
      Plate voltage
         Maximum
         Minimum
         Mean

      Current
         Maximum
         Minimum
         Mean
      Sparking rate mean              	  N/A
         Mean                     l/mln    606         606         606
       Inlet temperature mean           'C       78          80          79
       Exit temperature mean           	   i*-	  '_±	   '*•
       Pressure drop
         Maximum                  	   	  	   	
         Minimum                  	   	  	   	
         Mean                     	   N/fl	  N/fl
         Mean                      	   N/A         N/A
      L/G ratio
         Maximum
         Minimum                  	   	  _   	    	
         Mean                     	   0.70        0.70        HTTP"
      Influent pH (into IWS) .
         Maximum                  P_H	   6.8	  7.5	   7.3
         Minimum                   P_H	   6.3	  6.7          6.9
         Mean                      P_H	   6.6	  7.1	   7.1
      EffluentpH (out of IWS)                                     .
         Maximum                 P_H	   4.7         3.1          4.1
         Minimum                  Pjj	   2.9         2.9          3.3
         Mean                     P_H	   3.8         3.0          3.7

    Scrubbant blowdown rate            	   	   	   	
                                               178

-------
Table G-1.   Response to APCE Parameters, Form 6 "Summary of Test Results"
                                                                        Test No.
        Parameter                             Units            1
    IWS water flowrates
    1st stage IWS water flowrate                 L/min           322         322        321

    2nd stage IWS water flowrate                 L/min           142         142        142

    3rd stage IWS water flowrate                 L/min           142         142        142

    Total                                    L/min           606         606        606
   IWS current and voltage
   IWS Unit 1A-DC Current                    mA            23.3        23.2        23.5
   IWS Unit 1A-DC Voltage                    kV             30.5        30.0        29.1

   IWS Unit IB-DC Current                    mA            16.1        14.9        15.6
   IWS Unit IB-DC Voltage                    kV             31.2        30.8        29.4

   IWS Unit 2A-DC Current                    mA            104.9       94.5        109.8
   IWS Unit 2A-DC Voltage                    kV             27.9        29.0        26.2

   IWS Unit 2B-DC Current                    mA            101.1       94.2        94.2
   IWS Unit 2B-DC Voltage                    kV             28.8        29.0        25.9
                                                179

-------
Form 6. Summary of System Performance
    Test No. summary of  test results
           (if data for a run)
    Parameter                         Units
                  Data from each run or average for each test
                          (min
          Test  1       Test 2
    (min. 3 runs = 1 test)
    " "      Test J
    Performance
    Flue gas
       Flowrate (actual), mean

       Flowrate (STP), mean  (wet)
       Velocity (actual), mean( wet)
ppra—
    CO (corrected to 1% 02)
          Maximum
          Minimum
          Mean

    Paniculate emissions
       Actual emission rate
       Actual concentration
       % Isokinetic
       Concentration corrected to 1% O2
       Metal	
       Metal	
       Metal	
       Metal	
       Emission rate
       Into APCE
       Out from APCE
       % removal
          501
          IZ7T
       Velocity (STP)mean (wet)      m/s      10.5
    Hue gas composition (by volume)
       H20
       O2 (by volume, dry)
       N2 (by volume, dry)
       CO2 (by volume, dry)
       CO (by volume, dry)
       Total unburned hydrocarbons
       SOX
       NOX
32
10
8i
1 .
.4
./
.6
/
31. Z






         48
mg/rm'B   12.9
-- /l'-J   38.2
         59.5
508
12.3
                      10.5
                      32.4
                      8T74
71
                      22.1
                      64.4
100.4
                                    492
                                    TT78
             10,1
             32.4
                                   TTTl
                                   bU.b
                                    80
             15.8
             47.5
                                    75.4
                                             (continued)
                                                180

-------
Form 6. Summary of System Performance (concluded)
   Test No. summary  of  test results              Data from each run or average for eaeh test
         (if data for a run)                                    (min. 3 runs = 1 test)
   Parameter                       Units    Test 1     Test 2     Test 3     	
HCL
Emission rate
IntoAPCE
Out from APCE
% removal
ka/h
kg/h
%
1.06
200

99.47
0.64
156

99.59
1.29
153

99.16
   POHC input
      tn'rhlnrnpthylpnp        g/min    353
      tptrachlnrnpthylene      g/min    222
      tn'rhlnrnbpnzene	    g/min    82S_
   POHC emissions
     tri rhlnropt.hyl PPP         g/min   0.0082
     tptrar.hlnrnpthyl pnp       g/mi n   0.0036
     trirhlnrobpnzenp	    g/min   0.0166
   DRE for POHC
     trirhlnrnPthylene           %     99 998	   99,998      99,997
     t.P.t.rarhl nrnpthyl pnp         %     99.998      99.997      99.998
     tHrh1r>rnhpn7pnP            %     99.998      99.996      99.996
                                           181

-------
 Summary of Results
Runs 1-1,1-2, and 1-3
          182

-------
Form 4.  Summary of Test Conditions (Waste Feeds)
Test No. ]
(if data for a run)
Parameter each
Test Dates
Elapsed time average
Units 1~1

Data from each run or average for each test
(min. 3 runs = 1 test)
1-2V 1-3

5/12/88 5/12/88 5/13/88
min 120
120 120
Feed rate of each waste burned

   l.  SI  drummed (PCC)
      Size of containers
      Maximum
      Minimum
      Mean

   2.  SL  sludge  (PCC)
      Size of containers
      Maximum
      Minimum
      Mean

   3.  LI  aquoeous  (PCC)
      Size of containers
      Maximum
      Minimum
      Mean

   4.  12 Hi  Btu  (PCC)
      Size of containers
      Maximum
      Minimum
      Mean

   5.  L4 Hi  Btu  (SCC)
      Size of containers
      Maximum
      Minimum
      Mean

Total (mean) feed rate of all wastes to PCC

Total (mean) feed rate of all wastes to SCC
                                            55 gal
   Auxiliary fuel used (total)
      Fuel   natural  gas
      Fuel	
      Fuel	


kg/min
27.2



kg/mi n
8.32


kg/min

30.3


kg/min

2.19



kg/min
€C
5.90
68.0
CC
5.90
kg /min
5.71


 55 gal
                                                        26.5
                                                        8.32
                                                        30.3
                                                        2.23
                                                        5.75
                                                        67.4
                                                        5.75
5.70
 55 gal
             25.7
             9.08
             28.8
             2.27
             5.9B
             65.9
             5.98
5.71
                                           (continued)
                                              183

-------
Form 4.  Summary of Test Conditions (Waste Feeds) (concluded)
    Test No.     1	                                   Data from each run or average for each test
           .(if data for a run)                                            (min. 3 runs = 1 test)
    Parameter       each               Units    1-1	   1-2           1-3          	
       Metals and salts
        none	
       Organic Chloride

       Other materials of concern
                                                     184

-------
Form 5.  Summary of Operating Parameter Values
               JL
Test No..
       (if data for a run)
Parameter
                                    Units
                                            Run 1-1
        Data from each run or average for each test
                     3 runs = 1 test)
                         Run  1-3
Run
    PCC temperature
       Maximum
       Minimum
       Mean

    SCC temperature
       Maximum
       Minimum
       Mean
                                        942-
            94S-
                                                                9i€-
                                •c
                                •c
1,118
1,115
1,022
1,113
                                •c
1,020
1,049
1,019
1.038
1,032
    Combustion gas flowrate (identify on P&I or schematic where measured)
      • Actual T =	.p=   1 atm
       Maximum? quench outlet   	   	   	
       Minimum                      ->       	   	
       Mean
       @STP  T= 2Q'C
       Maximum
       Minimum
       Mean

    Waste feed pressure
    Atomizing fluid pressure
    Combustion air blower power
    ID fan power

    PCC pressure
       Maximum
       Minimum
       Mean

    SCC pressure
       Maximum
       Minimum
       Mean

    APCE operating conditions
    Quench
       Inlet temperature mean
       Outlet temperature mean
       Water feed rate
         Maximum
         Minimum
         Mean
                               m  /min 931

                       .p=  1 atm
            956
            845

m /min
psi _~

867 891
Not measured.
30 30
N/A N/A

787

30
N/A
Not measured.
                                       -T75~
            -2.6
            -2.5
                               mm FLO -8.0
            -8.4
            -7.6
                               	  Same as  SCC temperature.
                               "C      79          79	   77
                               L/min   852
            912
            965
                                            (continued)
                                              185

-------
Form 5. Summary of Operating Parameter Values (concluded)
               1
Test No. __
       (if data for a run)
Parameter
                                    Units
        Data from each run or average for each test
                (min, 3 runs = 1 test)
Run  1-1     Run 1-2     Run  1-3
    APGE (as applicable)
      Water/liquor flowrate
         Maximum
         Minimum
         Mean
      Inlet temperature mean
      Exit temperature mean
      Pressure drop
         Maximum
         Minimum
         Mean

      L/G ratio
         Maximum
         Minimum
         Mean

      Influent pH
         Maximum
         Minimum
         Mean

      Effluent pH
         Maximum
         Minimum
         Mean

    Scrubbant blowdown rate

      Nozzle pressure
         Maximum
         Minimum
         Mean

      Plate voltage
         Maximum
         Minimum
         Mean

      Current
         Maximum
         Minimum
         Mean

      Sparking rate mean
                                        See next page.
L/min  603
                                                     603
PH
PH
PH
                                        71
             72
I/in     0.65
                                                     0.63
                                 pH      6.3
             6.9
                                                     6.6
                                         6.3
             6.7
                                        4.1
            4.3
                                         2.9
             3.5
                                        3.6
            4.0
                                         N/A
                                         See next page.
                                         SPP npxt pagp.
                         603
                                 71
                         0.71
                                 6.6
                         6.1
                                 6.5
                                 4.2
                                 3.5
                                 3.8
                                         N/A
                                              186

-------
Table G-2.   Response to APCE Parameters, Addendum to Form 5
Parameter
IWS water flowrate
1st stage IWS water flowrate
2nd stage IWS water flowrate
3rd stage IWS water flowrate
Total
IWS current and voltage
IWS Unit 1A-DC Current
IWS Unit 1A-DC Voltage
IWS Unit IB-DC Current
IWS Unit IB-DC Voltage
IWS Unit 2A-DC Current
IWS Unit 2A-DC Voltage
IWS Unit 2B-DC Current
IWS Unit 2B-DC Voltage
Units
L/min
L/min
L/min
L/min
mA
kV
mA
kV
mA
kV
mA
kV

1-1
321
142
142
605
33.8
30.0
21.1
•31.1
94.2
28.2
105.4
28.8
Run No.
1-2
322
142
142
606
21.8
30.5
16.5
30.6
126.1
27.8
116.2
29.0

1-3
322
142
142
606
14.2
31.0
10.7
31.8
94.4
27.7
81.7
28.5
                                                  187

-------
Form 6. Summary of System Performance
    Test No.	
           (if data for a run)
    Parameter
Units
        Data from each run or average for each test
                  (min. 3 runs = 1 test)
1-1           1-2          1-3

Performance
Flue gas
Flowrate (actual), mean
Flowrate (STP), mean
Velocity (actual), mean
Velocity (STP) mean
Flue gas composition (by volume)
H20
O2 (by volume, dry)
N2 (by volume, dry)
CO2 (by volume, dry)
CO (by volume, dry)
Total unbumed hydrocarbons
SOX
NOx
3
m /min 866
m3/min 501

m/«s 7.1
t 3?.0
1 10.55
' «L 89.3
°L 7 ?
nnm 4^,2




866
508
12.3
7.2
33.0
10.60
RI .3
R.I
?0 3




827
492
11.8
7.0
32.2
10.81
81.3
7.9
34. Q






nnm
rr"1
   CO (corrected to 7% O2)
         Maximum
         Minimum
         Mean

   Paniculate emissions
      Actual emission rate              	
      Actual concentration              	
      % Isokinetic                    .  %   -
      Concentration corrected to 7% O2   mg/Nm
      Metal	     	
      Metal	:	     	
      Metal	     	
      Metal	     	
      Emission rate                    	
      Into APCE                      	
      Out from APCE                 	
      % removal                      	
         P.? n
         98.7
         80.2
             9Q.Q
              97.1
              65.5
98.8
32.8
                                               (continued)
                                                  188

-------
Form 6. Summary of System Performance (concluded)
   Test No.	
          (if data for a run)
   Parameter
            Units
1-1
                Data from each run or average for each test
                        (min. 3 runs = 1 test)
                     1-2 _    1-3
   HCL
      Emission rate
      IntoAPCE
      Out from APCE
      % removal
           g/min
           g/mi n
          Q.34
            9,520
            13. ft
            qq.43
7, ssn
17.fi
qq.31

      pprrhlnrnpthylpnp
        r
g/min     353
g/mi n
g/mip
                                                     345
                                            360
                                            7Qd
   POHC emissions
      trichloroethylene        g/min    0.014
      pprchloroethylene        g/min    0.0022
      t.n'r.h1ornhp7pnp	    g/mi n    0.0418
                                0:0069
                                0.0066
                                0.0017
                                 0.0036
                                 0.0020
                                 0.0064
      tnchloroethyl
ene
         99.9960     99.9980     99.9990
      perchloroethylene
      tnchlorobenzene
                                yy.yyyb
                                           189

-------
                                             Form 7. Method 5 and Paniculate Results3
CO
o
Parameter
Sample time
Sample volume^
Stack gas volumetric flowrate
Stack gas volumetric flowrate^
Stack gas temperature
Stack gas moisture
Oxygen concentration0
Carbon dioxide concentration0
Percent isokinetic
Paniculate collected
Paniculate concentration
Paniculate concentration corrected
to 7% oxygen
Unitsa
min
Mm3
3. .
m /mm
Nm /min
•c
% vol.
%
%
%
mq
mq/Nm
mg/Nm


1-1

120
2.013
875
507
71
32.0
10.8
7.2
98.7
117. 0
58.1
80.?

Test or Run No.
1-2

120
2.015
892
515
72
33.0
10.6
8.1
97.1
98.?
48.7
fifi.fi


1-3

120
1.914
830
481
71
32.2
10.7
7J9
98.8
4fi.3
?4 ?
M. 8

                                             a Either metric or English units are acceptable as long as consistency is maintained throughout the report.
                                             b Dry standard basis.
                                             c From Orsat analysis.

-------
             Form 8a. Chlorine Input Rates
CD
Test or run no. 1 ~ 1


Waste/fuel stream
Drummed waste
(SI)
Sludae (SL)
Organic liciuid-
kiln (L2)
Organic liquid-
scc (L4)
Wa«;tpwat.pr-
kiln (LI)
Natural qas


Feedrate
(kg/min)
27.2

8.32
2.19

5.90

30.. 1

5.71

Chlorine
concentration
(%)
2.29

0.0098
15.4

?fi.6

0.200

N/A

Chlorine
input rate
(g/min)
624

0.9


1,570

fii


Test or run no. 1-2


Feedrate
(kg/min)
26.5

8.32
JL23_

5.75

30.3

S 70

Chlorine
Concentration
(%)
2.21

0.0096
15.2

2fi.?

n IQQ

N/A

Chlorine
input rate
(gMin)
585

0.8
329_

1 , 530

fin


Test or run no. 1-3

Chlorine .
Feedrate concentration
(kgAnin) (%)
25 7 2 22

9.08 0.0094
2.27 14.7

FJ.QR 2fj.5

?ft.R 0 200

5.71 N/A


Chlorine
input rale
(g/min)
570

0.8
337

i .RQO

fin


                  Total
                                                         2.590
78.8
2.520
2,550

-------
              Form 8b. HCI Emissions3.13 and Removal Efficiency
CO
ro
Sample Sample HCI Stack gas Cl~ emission
Run No. period volumec HCI collectedd concentratione flow ratef rate
1-1 120 2.013 9.15 ( 18.4 ) 507 9.34 0.560
1-2 120 2.015 13.35 ( 26.9 ) 515 13.8 0.831
1-3 120 1.914 19.14 (36.6 ) 481 17.6 1.057
HCI emission HCI removal
rateg effciency (%)
1.24 99.64
1.83 99.45
2.33 99.31
( ,
( }
( }
( >
( }
( }
( )
( }
Blank value 0.12


              a Either metric or English units are acceptable as long as consistency is maintained throughout the report.
              b This table is formatted to use chloride results from a single MM5 train (only one chloride emission sample is required per run).  If two MM5 trains are run,
                both sets of HCI data should be reported.
              c Sample volume is dry standard liters of stack gas.
              d Show value corrected for blank in parentheses.
              e Blank corrected as applicable.
              f Stack gas flow rate is dry normal (standard) m3/min.
              g Chloride emissions (Ib/h) x 1.03.

-------
             Form 9b.POHC Input Rate, [RunJ No.    1-1
CO
CO
Waste feedrate
Waste/Fuel stream (kg/min)a
SI drummed 27.2

SL sludge 8.32

LI aqueous 30.3

12 Hi Btu lid (PCC) 2.19
b POHC concentration0 (%)a/feedrate (g/min)a DRE
TCE PCF. TCB

d <0.0002 <0.0002

e 	 	
d < 0.0003 <0.0004

e ~ 	
d <0.0017 <0.0019


d <0.0016 10.0

1.97
536
<0.0006


< 0.0028


<0.0024
e 	 220 	
L4 Hi Btu liq (SCCl 5.90

Auxiliary fuel, natural 5.71
qas

d 5.98 
-------
Form Sb.POHC Input Rate, [Run] No.    1-2
Waste feedrateb POHC concentration0 (%)a/feedrate (g/min)a ORE
Waste/Fuel stream flcp/muOa TCE PCE TCB

SI drummed 26.5 d < 0.0002 < 0.0002


SL sludae 8.32 d <0.0003 ^0.0004
e 	 	
11 aqueous 30.3 d /O.D017 <0.001Q
e 	 	

1.97
522
<0.0006

CO.OD2R

i? ni Rtu liq (prr.) '.?.? d 
-------
              Form Sb.POHC Input Rate, [Run] No.    1-3
CO
Ul
Waste feedrate1
Waste/Fuel stream (kg/min)a
SI drummed 25.7

SL sludge 9.08

LI aqueous 28.8

L2 Hi Btu liq (PCC) 2.27
b POHC concentration0 (%)a/feedrate (g/min)a DRE
TCE PCE TCB

d 0.0002 0.0002

e
d 0.0003 0.0004

e 	
d 0,0017 0.0019

e ~
d 0.0016 10.0

1.97
506
0.0006


0.0028


0.0024
e 	 227
L4 Hi Btu liq (SCO) 5.98

Auxiliary fuel, natural 5.71
gas
d 5.98 0.0018
e 347 	

d 	 	

e
5.06
293




d
e
Total POHC feedrate
347 227

799

              a  Give units.
              b  Give feedrate measured during this run/test.
              c  Give concentration measured from sample taken during this test/run.
              d  Give concentration at POHC in each waste.
              e  Give feedrate of each POHC.

-------
Figure G-1. Strip chart recording of combustion temperatures - run 1-1.

  1000
  1500
     ^^
£ 2000
o
  Y~r'~A^^
J?       K.              ••.
                                 8
                       8
                                                             S
  2500
          I  I   t  1   I   i  i   I  I   I  I   I   I  i   I  I   III
                                196

-------
Figure G-2.  Plot of corrected CO readings from data logger 1-min averages - run 1-1;
    ,- 100'
       90-
                                            CO (Corrected 7% OJ vs Time
         1250 1300 1310 1320 1330 1340  1350  1400 1410  1420 1430  1440 1450 1500 1510 1520 1530 1540 1550
                                                     Minutes
                                                   197

-------
       I
       "8
o

2
                                   S*N^
                     CO
                                  CTi
                                        01
                                        Lf)
                                              co
                                              00
                                              CM
r-.
o
in
                                                  a  e

                                                  I 8
                                                              CTi
CO


CTi
                                                                          en
                                                              —1    CS     M
                                                     I
                                                                                CM


                                                                                CTl
                                                                                CM
                                                                                             o
                                                                                             o
                                                                                             ID
                                                                                       s^

                                                                                \    3
                                            a>
                                            3^
                                         d  E
                                         a .1
                                   £ "8
                                                                                                                   .a
                                                                           S
                                                                198

-------
                 Form 9a. POHC Emissions
                                                                    Form 9a. POHC Emissions
                                       Sample     Sample
                           Trap pair    period     volume
                 Ron No.  (forVOST) (min  )b (J	Jb
                                                                                          Mass of each POHC collected
                                                 TC-E-
                                                                                             J»      (_
                                                                                               J"        L
                                     -M	     19.a    _135_<
                 	      2      4Q	     19.9     67     (

                 	      3      _4Q_	     20.0

                         Total/average*  120        59.7         	

                 POHC concentration f JJfl/1      ft                 4.?
                 Stack gas flow rate (pm  /min
                 Emission rate (J
                                                                 7fi
               if nm  /min ft
               i/min  ft
CD
CD
         Total/average*1

POHC concentration (	
Stack gas flow rate (	
Emission rate (	
                                              J>
                 Average blank value^ (	
                 Standard deviation1* (	
                 Range of blank values^ (_
                              Jb
                 Note:  This format is structured for VOST results. It may be used for MM5, a similar format would be used for integrated bag sampling for volatiles.  Guidance for blank correction is provided in the
                        "Practical Guide—Trial Bums for Hazardous Waste Incinerators," Final Report, EPA-600/2-86-Q50,1986.
                 Note:  Use parentheses to present results if two collectors are used in series (i.e., dual adsoprtion tubes on VOST).
                     a Either metric or English units are acceptable as long as consistency is maintained throughout the report.
                     b Sample volume is dry standard liters of stack gas.         d totals for sample period, volume, and amount collected; averages for concentration, flowrate, and emissions rate.
                     c Stack gas flowrate is dry normal (standard) m3/min.       e Indicate whether all (both field blanks and trip blanks) are used or whether only field blanks are used.

-------
Table G-3. Combustion Temperature Data Taken From Strip Chart - Run 1 '••"
Time
(niin)
1250
1251
1252
1253
1254
1255
1256
1257
1258
1259
1300
1301
1302
1303
1304
1305
1306
1307
1308
1309
1310
1311
1312
1313
1314
1315
1316
1317
1318
1319
1320
1321
1322
1323
1324
1325
1326
1327
1328
1329
1330
1331
1332
1333
1334
1335
sec
Temp
(°F)
1889
1894
1893
1872
1913
1925
1898
1901
1906
1917
1918
1892
1904
1919
1899
1889
1898
1919
1923
1889
1906
1927
1932
1903
2004
1936
1920
1893
1904
1921
1922
1899
1899
1896
1911
1878
1880
1901
1901
1885
1880
1887
1900
1886
1890
1885
Kiln
Temp
(°C)
1688
1689
1623
1595
1693
1730
1661
1616
1613
1743
1699
1653
1677
1693
1699
1660
1678
1700
1710
1682
1693
1710
1679
1564
1685
1743
1670
1591
1613
1741
1722
1671
1669
1702
1694
1649
1679
1695
1703
1693
1674
1724
1624
1589
1603
1685
Time
(min)
1336
1337
1338
1339
1340
1341
1342
1343
1344
1345
1346
1347
1348
1349
1350
1351
1352
1353
1354
1355
1356
1357
1358
1359
1400
1401
1402
1403
1404
1405
1406
1407
1408
1409
1410
1411
1412
1413
1414
1415
1416
1417
1418
1419
1420
1421
sec
Temp
(°F)
1894
1891
1885
1894
1927
1929
1941
1967
2045
1985
1980
1973
1985
1983
1955
1971
1961
1956
1946
1969
1966
1964
1936
1954
1961
1948
1931
1924
1926
1940
1899
1900
1905
1909
1882
1903
1911
1901
1898
1922
1921
1905
1877
1900
1893
1908
Kiln
Temp
(°C)
1686
1633
•1563
1670
1710
1679
1602
1646
1736
1705
1666
1694
1688
1674
1650
1689
1694
1682
1680
1695
1714
1694
1569
1675
1727
1649
1612
1620
1738
1705
1671
1680
1680
1667
1644
1678
1722
1680
1663
1674
1687
1683
1635
1599
1602
1674
(continued)
   200

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Table G-3. Combustion Temperature Data Taken From Strip Chart - Run 1 (concluded)
Time
(min)
1422
1423
1424
1425
1426
1427
1428
1429
1430
1431
1432
1433
1434
1435
1436
1437
1438
1439
1440
1441
1442
1443
1444
1445
1446
1447
1448
1449
1450
1451
1452
1453
1454
1455
1456
1457
1458
1459
1500
1501
1502
1503
1504
1505
1506
1507
1508
sec
Temp
(°F)
1888
1881
1909
1895
1888
1894
1895
1892
1880
1878
1909
1908
1923
1932
1927
1926
1903
1906
1921
1925
1933
1920
2030
1954
1942
1918
1915
1936
1947
1931
1929
1947
1928
1910
1910
1932
1932
1911
1930
1934
1934
1907
1929
1944
1947
1909
1918
Kiln
Temp
(°C)
1692
1624
1577
1656
1746
1646
1601
1639
1736
1705
1675
1694
1673
1674
1647
1712
1696
1706
1681
1685
1716
1703
1562
1661
1748
1670
1628
1645
1763
1726
1659
1702
1679
1673
1663
1711
1687
1699
1675
1677
1722
1692
1682
1584
1572
1573
1590
Time
(min)
1509
1510
1511
1512
1513
1514
1515
1516
1517
1518
1519
1520
1521
1522
1523
1524
1525
1526
1527
1528
1529
1530
1531
1532
1533
1534
1535
1536
1537
1538
1539
1540
1541
1542
1543
1544
1545
1546
1547
1548
1549
1550



AVG
MIN
MAX
sec
Temp
(°F)
1926
1936
1910
1901
1925
1984
1921
1915
1930
1934
1909
1912
1908
1935
1921
1910
1931
1945
1939
1942
1940
1956
1954
1917
1936
1945
1950
1886
1898
1892
1876
1904
1918
1891
1893
1911
1929
1920
1893
1908
1905
1914



1919.6
1872
2045
Kiln
Temp
(°C)
1564
1592
1607
1612
1608
1668
1701
1647
1570
1684
1737
1679
1615
1614
1738
1697
1676
1678
1709
1674
1643
1705
1709
1683
1687
1708
1702
1664
1573 '
1674
1714
1671
1628
1614
1760
1715
1661
1704
1707
1672
1663
1704



1670.2
1562
1763
201

-------
Table G-4. GEM Data From Data Logger Files -
Time
(min)
1250
1251
1252
1253
1254
1255
1256
1257
1258
1259
1300
1301
1302
1303
1304
1305
1306
1307
1308
1309
1310
1311
1312
1313
1314
1315
1316
1317
1318
1319
1320
1321
1322
1323
1324
1325
1326
1327
1328
1329
1330
1331
1332
1333
1334
1335
1336
Run 1
02
(%)
10.59
10.49
10.45
10.35
10.47
10.30
10.20
10.31
10.37
10.27
10.38
10.63
10.64
10.61
10.52
10.50
10.59
10.51
10.54
10.55
10.55
10.47
10.64
10.46
10.59
10.63
10.50
10.49
10.48
10.50
10.77
10.60
10.72
10.51
10.62
10.56
10.36
10.33
10.51
10.32
10.45
10.34
10.50
10.36
10.45
10.37
10.42

CO
(ppm)
51.46
52.03
53.70
57.74
51.96
53.85
53.29
52.87
52.15
54.04
56.07
54.78
48.36
55.18
56.03
57.69
51.60
54.98
52.38
51.18
51.94
56.09
51.96
57.20
51.50
54.47
57.91
57.77
54.84
51.92
56.53
51.07
56.17
53.73
48.40
51.48
52.99
52.73
51.69
53.52
47.68
47.09
45.75
52.35
48.23
48.42
46.15

CorrCO
(ppm)
69.2
69.7
71.1
76.4
68.8
70.4
69.7
69.1
68.2
70.7
74.2
73.4
64.8
73.9
75.1
77.3
69.1
73.7
70.2
68.6
69.6
75.2
69.6
76.6
69.0
73.0
77.6
77.4
73.5
69.6
76.7
69.3
76.2
72.0
64.8
69.0
70.1
69.8
68.4
70.8
63.1
62.3
60.5
69.3
63.8
64.1
61.1
(continued)
   202

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Table 6-4. GEM Data From Data Logger Files
Time
(min)
1337
1338
1339
1340
1341
1342
1343
1344
1345
1346
1347
1348
1349
1350
1351
1352
1353
1354
1355
1356
1357
1358
1359
1400
1401
1402
1403
1404
1405
1406
1407
1408
1409
1410
1411
1412
1413
1414
1415
1416
1417
1418
1419
1420
1421
1422
1423
- Run 1 (continued)
02
(%)
10.51
10.50
10.64
10.47
10.50
10.59
10.44
10.50
10.35
10.41
10.34
10.53
10.62
10.88
10.85
10.80
10.75
10.64
10.63
10.62
10.64
10.62
10.58
10.60
10.64
10.45
10.64
10.37
10.48
10.45
10.37
10.49
10.67
10.82
10.71
10.60
10.66
10.90
10.81
10.62
10.51
10.59
10.52
10.64
10.54
10.64
10.63

CO
(ppm)
47.93
49.63
47.48
52.55
51.55
47.49
50.99
47.09
48.07
47.82
42.47
47.40
47.14
55.84
49.51
47.90
51.62
46.26
52.20
47.81
48.16
48.14
42.87
44.69
49.88
45.63
49.40
48.55
46.77
47.17
45.82
45.31
50.20
43.31
46.15
48.64
43.15
42.37
42.05
48.53
49.76
44.14
41.78
45.32
45.50
36.92
38.69

CorrCO
(ppm)
63.4
65.7
63.6
70.4
69.1
63.6
67.5
62.3
63.6
63.3
56.2
63.5
63.9
76.7
68.9
65.8
70.9
62.7
70.8
64.8
65.3
65.3
58.1
60.6
66.8
61.1
66.2
64.3
61.9
62.4
60.6
60.0
68.1
59.5
62.6
66.0
58.5
58.2
57.8
65.8
66.7
59.1
56.0
60.7
61.0
49.5
51.8
(continued)
   203

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Table G-4. CEM Data From Data Logger Files
Time
(min)
1424
1425
1426
1427
1428
1429
1430
1431
1432
1433
1434
1435
1436
1437
1438
1439
1440
1441
1442
1443
1444
1445
1446
1447
1448
1449
1450
1451
1452
1453
1454
1455
1456
1457
1458
1459
1500
1501
1502
1503
1504
1505
1506
1507
1508
1509
1510
- Run 1 (continued)
02
(%)
10.54
10.60
10.57
10.61
10.61
10.61
10.77
10.61
10.56
10.62
10.43
10.51
10.46
10.51
10.42
10.49
10.65
10.47
10.50
10.57
10.56
10.62
10.55
10.61
10.51
10.54
10.52
10.63
10.45
10.58
10.57
10.46
10.68
10.60
10.61
10.59
10.74
10.75
10.72
10.62
10.70
10.58
10.63
10.47
10.56
10.48
10.56

CO
(ppm)
40.80
38.17
41.49
38.45
42.41
40.68
40.86
43.21
41.75
39.76
37.22
36.14
37.02
45.39
40.65
39.62
37.28
36.91
43.00
35.95
43.24
40.83
42.15
41.04
36.05
38.97
37.61
37.12
39.85
38.83
39.44
42.01
47.83
42.34
41.65
35.56
46.86
41.75
38.39
48.95
37.16
35.39
36.67
39.52
54.24
40.96
38.23

Corr CO
(ppm)
54.7
51.1
55.6
51.5
56.8
54.5
55.4
58.6
55.9
.53.3
49.3
47.8
49.0
60.1
53.8
53.1
50.0
49.5
57.6
48.2
57.9
54.7
56.5
55.0
48.3
52.2
50.4
49.7
53.4
52.0
52.8
56.3
64.9
57.4
56.5
48.2
64.4
57.3
52.7
66.4
50.4
47.4
49.1
52.9
72.7
54.9
51.2
(continued)
   204

-------
Table G-4. CEM Data From Data Logger Files
Time
(min)
1511
1512
1513
1514
1515
1516
1517
1518
1519
1520
1521
1522
1523
1524
1525
1526
1527
1528
1529
1530
1531
1532
1533
1534
1535
1536
1537
1538
1539
1540
1541
1542
1543
1544
1545
1546
1547
1548
1549
1550
MINIMUM
MAXIMUM
AVERAGE
- Run 1 (concluded)
02
(%)
10.48
10.49
10.48
10.47
10.53
10.63
10.55
10.21
9.94
10.09
9.96
10.12
10.25
10.33
10.45
10.73
10.86
10.84
11.02
10.86
10.98
10.75
10.80
10.77
10.74
10.71
10.77
10.74
10.62
10.74
10.63
10.64
10.49
10.41
10.51
10.47
10.34
10.35
10.61
10.56
9.94
11.02
10.55

CO
(ppm)
38.05
46.51
39.53
41.92
36.59
38.05
40.40
38.37
38.21
39.88
39.82
51.09
49.26
44.63
49.42
52.33
41.34
48.58
50.81
49.02
48.69
47.68
49.45
42.01
46.30
44.89
44.68
46.89
43.02
43.36
44.23
45.70
43.04
43.45
47.26
44.25
41.33
46.39
46.71
45.59
35.39
57.91
46.23

CorrCO
(ppm)
51.0
62.3
53.0
56.2
49.0
51.0
54.1
49.6
48.2
50.9
50.8
66.0
63.6
58.4
65.4
71.0
56.8
67.6
70.7
68.2
67.7
65.5
67.9
57.7
63.6
60.9
60.6
63.6
58.3
59.6
60.0
61.2
57.0
57.5
62.5
58.6
54.7
61.4
62.6
61.1
47.4
77.6
62.0
                  atl.S. GOVERNMENT PRINTING OFFICE: 1989*48-163/87067
205

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