vvEPA
                        United States
                        Environmental Protection
                        Agency
EPA/540/S5-89/007
April 1989
                        SUPERFUND INNOVATIVE
                        TECHNOLOGY EVALUATION
                         Technology  Demonstration
                         Summary

                         Shirco  Pilot-Scale  Infrared
                         Incineration System  at the  Rose
                         Township Demode Road
                         Superfund Site
                         Under the Superfund Innovative
                        Technology Evaluation or SITE
                        Program, an evaluation was made of
                        the  Shirco Pilot-Scale Infrared
                        Incineration  System during  17
                        separate test runs under varying
                        operating conditions. The tests were
                        conducted at  the Demode Road
                        Superfund  site in  Rose Township,
                        Michigan using  1,799 kg (3,967 Ib) of
                        soils contaminated with  poly-
                        chlorinated biphenyls (PCBs) and
                        other organics, and lead and other
                        heavy metals. The report includes a
                        process description of the unit, unit
                        operations data,  sampling and
                        analytical procedures  and data, and
                        an overall evaluation of performance
                        and energy consumption.
                         The Shirco  Infrared Incineration
                        System uses electricity for infrared
                        heating rods which heat the soil and
                        desorb or  incinerate the organic
                        contaminants, followed by a conven-
                        tional,  propane-fired combustion
                        chamber to complete the destruction
                        of gaseous  organic compounds. The
                        system  was  evaluated  for
                        effectiveness  in  removing and
                        destroying organic contaminants and
                        reducing the  mobility of  metal
                        contaminants under both standard
and varied operating parameters. The
achievement of applicable regulatory
standards and the effect of operating
conditions on energy consumption
were also assessed.
 The results show that the unit
achieved destruction and removal
efficiencies (DREs)  for  PCBs
exceeding  99.99%,  based  on
detection limits. Several semivolatile
and volatile organic compounds were
measured in the stack gas at very low
levels (parts per billion) and may be
products of  incomplete combustion
(PICs). The unit achieved regulatory
standards for acid gas removal and
particulate emissions.  Levels of
residual PCBs in the  furnace ash
were less than 0.2 ppm under most
unit operation conditions. The
majority of the heavy metals
remained in the  furnace ash, but
there was no evidence of a decrease
in the mobility of lead as  a result of
treatment. Also,  residual  heavy
metals  were measured  in the
scrubber  water effluent. The
optimization of the heat content of
the waste, retention time, and primary
combustion  chamber  temperature
can significantly reduce  energy
consumption and cost.

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  This Summary was developed  by
EPA's  Risk Reduction  Engineering
Laboratory,  Cincinnati,  OH,  to
announce  key findings  of the  SITE
Program demonstration  that is  fully
documented  in two separate reports
(see ordering information at back).

Introduction
  In response  to  the  Superfund
Amendments and Reauthorization Act of
1986   (SARA),  the  Environmental
Protection  Agency's  Office of Research
and Development  (ORD)  and Office of
Solid Waste and Emergency Response
(OSWER)  have established a  formal
program to accelerate  the development,
demonstration, and  use of new  or
innovative technologies as  alternatives to
current  containment  systems  for
hazardous  wastes. This new  program is
called Superfund Innovative  Technology
Evaluation  or SITE. The principal  goal of
the SITE program is  to demonstrate new
technologies in the  field  and develop
reliable economics  and  performance
information.
  The  SITE program  demonstration of
the Shirco Pilot-Scale Infrared  Incin-
eration  System for  thermal treatment
developed by  Shirco  Infrared Systems,
Inc. of Dallas, Texas, was conducted at
the Demode  Road  Superfund  Site in
Rose Township, Michigan. The Demode
Road   site is a  12-acre waste site
previously  used to bury, dump, and store
industrial wastes such  as  paint sludges,
solvents, and other  wastes  containing
PCBs,  oils and greases,  phenols,  and
heavy  metals .  PCBs  and lead are the
principal contaminants in the soil used for
the test of the Infrared System.
  The  test  was   conducted  from
November 2-13, 1987  and treated  1,799
kg  (3,967 Ib) of contaminated soil under
various test conditions. The  major
objectives  of this demonstration were to
determine the following:

• ORE levels for PCBs and the presence
  of PICs in the stack gas.  The regulatory
  standards are 99.99% ORE under the
  Resource Conservation  and Recovery
  Act (RCRA) and 99.9999%  ORE under
  the  Toxic Substances and Control Act
  (TSCA).

• Level of hydrogen chloride (HCI) and
  particulates  in the  stack gas. The
  RCRA standard for  HCI in the  stack
  gas is 1.8 kg/hr (4 Ib/hr) or 99 wt% HCI
  removal  efficiency.  The RCRA standard
  for  paniculate emissions in the  stack
  gas is 180 mg/dscm (0.08 gr/dscf).
• Level of residual PCBs  in the furnace
  ash at  normal and  varied  operating
  conditions.

• Mobility  of  heavy metals,  particularly
  lead, in the furnace ash as compared to
  the feed.

• Mobility of heavy metals in the furnace
  ash  as   compared  to the  RCRA
  Extraction Procedure Toxicity (EP Tox)
  Characteristic  (as measured by the  EP
  Tox test) and  the  proposed Toxicity
  Characteristic  (as  measured  by the
  Toxicity  Characteristic  Leaching
  Procedure (TCLP)).

• Level of  residual  heavy metals and
  organic compounds, and other physical
  and chemical  characteristics in the
  scrubber  water  discharged  from the
  unit.

• The operating  conditions that reduce
  energy  consumption   without
  decreasing soil  decontamination
  effectiveness.

• Effect  of  varying operating conditions
  on residual  levels of heavy metals and
  organics in  the furnace ash versus the
  levels in the feed.

• Adherence  of  the  quality  assurance
  (QA) procedures to the requirements of
  the RREL approved QA Project Plan
  (Category  II),  as  defined  by  the
  Document No.  PA QAPP-0007-GFS,
  "Preparation  Aid  for  HWERL's
  Category  II  Quality Assurance Project
  Plans", June, 1987.

Feed Preparation
  The demonstration test used soil from
an  area of  the  site that was highly
contaminated  with  PCBs  and lead,  as
determined  in  the  original  remedial
investigations performed  at  the  site.
Pretest sampling and  analysis further
identified  those  sectors within the area
most highly contaminated with PCBs and
lead for excavation.  Other organics and
heavy metals  were also present in these
sectors.  Soil  from these sectors to  be
used as feed  for the test was excavated
and mixed  into  a pile using a front-end
loader, and then  screened to  remove
aggregate  and debris greater than one
inch in diameter. The screened soil was
drummed and transferred to a designated
zone adjacent to the test unit. Two drums
of soil were blended with 3 wt% fuel oil to
be  used for several of  the test  runs to
investigate the effect of increased feed
heating value  on overall  unit performance
and  energy  consumption  at varying
operating conditions.
Process Description
  The  Shirco  Pilot-Scale  Infrared
Incineration System  consists of a waste
feed system,  an  (electric)  infrared
primary combustion  chamber, a supple-
mental propane-fired secondary combus-
tion  chamber,  a  venturi scrubber
emissions  control system,  an exhaust
system, and a data collection and control
system, all enclosed  in a 45-ft trailer. The
system process flow and the overall 250
ft x 100 ft test site layout are presented
schematically  in  Figures  1  and  2,
respectively.
  During the test,  the feed material was
transferred from  the  drums to  pails,
weighed,  and then  fed manually to a
hopper  mounted  over a metering
conveyor  belt.  The waste was  fed  at a
controlled  rate through a sealed feed
chute onto the  incinerator conveyor  (a
tightly woven wire belt which moved the
waste  material  through the  primary
combustion chamber). The conveyor belt
speed can be  adjusted to achieve  feed
residence times in the PCC from 6 to 60
min.  Typically  residence times  range
from  10 to 25  min. The depth of  the
waste on  the conveyor  belt  ranged from
one to one and a half inches.
  The  primary combustion  chamber
(PCC) is a rectangular  box  insulated by
layers of ceramic fiber. Combustion air is
supplied  to  the  primary  combustion
chamber through a series of air ports at
points along the length  of the chamber .
The  gas  flow  in the  incinerator  is
countercurrent to the  conveyed  feed
material.  Electric  infrared  heating
elements  installed above the conveyor
belt  heat the waste to  the  designated
temperature  (nominally  1600°F),  which
results  in  desorption or incineration  of
organic  contaminants  from the feed.
Rotary rakes gently  turn the material to
ensure  adequate  mixing  and complete
desorption. When the  thermally treated
soil,  now  referred to  as furnace  ash,
reaches the discharge end of the PCC, it
drops off the belt through a chute and
into  an enclosed  hopper and discharge
storage drum. The drums of furnace ash
are then stored for final disposal.
  Exhaust gas containing the desorbed
contaminants  exits  the  primary
combustion chamber into a secondary
combustion  chamber  (SCC)  or
afterburner, where a  propane-fired burner
combusts  residual  organic  compounds
into C02, CO, HCI, and  H20. The SCC is
typically operated at 2200°F and a gas
residence time  exceeding  2  sec.
Secondary air  is supplied  to  ensure
adequate excess  oxygen  levels  for

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                                                                            Fencing
                                                                                                                                       X — X—
                                                Exclusion Zone
                            Drum Storage Area
                              • Waste Feed
                              • Ash
                              • Slowdown Water
                              • Empty Drums
Shirco Pilot-Scale Demonstration Unit Trailer
       •  Waste Feed
          Transfer—
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                                                                      Burner Forced
                                                                        Air Blower
                                                                                                                         Control Cabinet
                                                                                                                         Belt Speed Control
                                                                                                                         Burner Control
                                                                                                                         Light Panel
                                                                                                                         Motor Control Center
                                                                                                                         Transformer
                                                                                                                         Electrical Service
                                                                                                                         HEPC
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  Reduction      \
   Zone
/    /   /   /

 At Grade
                                                                                             Makeup Water
                                                                                              from Water
                                                                                             Supply Trailer
Figure  1.    System process flow.

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                                                                                              Waste Site
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Figure 2.   Overall test site
complete combustion.  Exhaust gas from
the secondary combustion chamber then
is  quenched by  a water-fed  venturi
scrubber emissions control  system  to
remove  particulate  matter and acid
gases. An induced draft fan transfers the
gas to the exhaust stack for discharge to
the atmosphere.
  The same trailer housing the thermal
system also contains the control panel for
the  main unit, and  data  collection
indicators  and   recorders.  Safety
interlocks also are  integrated into  the
trailer-mounted  unit  to  automatically
correct abnormal operating  conditions,
maintain  system performance,  and  if
necessary, shut down feed and heat input
to the unit.

Test Procedure
  In order to meet the objectives of the
demonstration test (see Introduction),  a
total of 17  test  runs were  conducted.
Three runs were  performed under design
                                                                        operating  conditions to assess overal
                                                                        unit  operation and  system performanct
                                                                        (Phase  \), and  14 runs  were conductec
                                                                        under varying operational  parameters  tc
                                                                        evaluate  their  effect  on   systerr
                                                                        performance and  energy consumptior
                                                                        (Phase II).
                                                                          The  Phase \ runs were conducted  a
                                                                        1600°F PCC temperature, a 2200°F SCC
                                                                        temperature, and a PCC residence time
                                                                        of 20 min.  Each of the three runs wa;
                                                                        sufficiently  long  (six to ten  hours)  tc

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gather a large enough sample  of stack
gas to analyze it for PCBs. An additional
run was conducted at the  same operating
conditions to  obtain specific  stack
samples that  had not been successfully
collected during two of the previous runs.
  The  Phase  II runs were conducted for
approximately one hour under varied
operating  conditions that included  the
PCC temperature (900, 1200, 1400, and
1600°F), SCC temperature (1800 and
2200°F), PCC feed residence time (10,
15, 20, and  25 minutes),  and PCC
combustion air flow (on,  off to  simulate
oxidizing or non-oxidizing  (pyrolytic) PCC
atmosphere).
  For the  Phase I  runs,  samples were
taken  of  the feed, scrubber  makeup
water,  furnace ash,  scrubber  water, and
scrubber  solids. These  streams were
analyzed for  PCBs, dioxins and furans,
metals, organics, and other physical and
chemical  properties  and  components
specific to the characterization  of each
sampled matrix. In  addition, the EP Tox
and TCLP  leaching  tests were performed
on these sampled  streams (exclusive of
scrubber water makeup) and the extracts
were evaluated for metals. Samples were
also taken of  the upwind and downwind
ambient air, PCC offgas,  and stack gas.
Ambient air upwind  and downwind of the
unit was monitored  for PCBs  and heavy
metals by  high volume samplers. For the
stack  gas and PCC  offgas,  several
sampling  methods were employed,
including an EPA Method 5 for paniculate
matter (and subsequent metals  analysis
of particulates) and hydrochloric acid;  a
Source Assessment Sampling  System
(SASS)  for  semivolatile organic
pollutants,  PCBs, dioxins  and furans;  a
Volatile Organic Sampling Train (VOST)
for volatile organic pollutants; a  Modified
Method  5 for  soluble  chromium;
continuous emission  monitoring  for
oxygen,  carbon  dioxide,  carbon
monoxide,  oxides of nitrogen, and total
hydrocarbons;  and an   experimental
method for vaporous  lead  emissions in
the PCC offgas.
  For the  Phase II  runs, samples were
taken of the feed, furnace ash, scrubber
water, scrubber solids, PCC offgas, stack
gas, and upwind and downwind  ambient
air. EPA Method 5 was  used again  to
sample stack  gas  and PCC  offgas  but
was analyzed  only  for particulate matter.
In addition, throughout the Phase II tests,
the stack  gas  and PCC  offgas were
continuously  monitored for  oxygen,
carbon dioxide, carbon monoxide, oxides
of nitrogen, and total hydrocarbons. All of
the remaining sampled  streams were
analyzed for PCBs, dioxins and furans,
metals, and other physical and chemical
properties and components specific to
the characterization  of  each sampled
matrix. In addition, the EP Tox and TCLP
leaching tests were performed on these
samples and the extracts were evaluated
for metals.
  All of the sampling and analytical work
was  conducted  in accordance  with
QA/QC  Category  II and include  data
quality credibility  statements for  the
precision  and accuracy of  the  data
reported.
Results and Discussion
  A  detailed  summary  of  the SITE
demonstration test results is presented in
Table 1.  Based on  the  test  objectives
outlined in the Introduction, the following
results were obtained.

• Characteristics of the Feed

    Based on data  from the previous
  remedial investigation  of the  site,  a
  specific area  within  the  site was
  identified  with   the  highest
  concentrations of both PCBs and lead,
  the major soil contaminants of concern.
  The  remedial  investigation  also
  described the soil  as  a dry,  brown,
  sandy,  and  silty  clay  topsoil  which
  upon excavation  proved  to  be an
  accurate observation. Subsequent
  pretest  sampling and analysis  of the
  specific area of  the  site  identified
  particular sectors  with  the  highest
  contamination of PCBs and  lead. A
  composite  sample of all the  sectors
  within the area indicated a 7.8 pH, 9.0
  wt.% moisture, 81  wt.% ash, less than
  1000 Btu/lb high heating value,  and  a
  0.95 g/cc   density.  The  composite
  sample contained  570  ppm  of total
  PCBs  and  580  ppm  lead  (elemental
  lead after digestion and conversion to
  inorganic form). A composite sample of
  the 10  sectors chosen  for  excavation
  contained 626 ppm PCBs, 560 ppm of
  lead, 55 ppb of tetrachlorodibenzo-p-
  dioxm  (TCDD),  and  4.2 ppb  of
  tetrachlorodibenzofuran (TCDF). Once
  the feed  excavation  was  begun, it
  became evident that  the  front-end
  loader could not confine its  large-scale
  activities to the 10  specific sectors and
  an area comprising 14 specific sectors
  was excavated  for  the unit's  feed
  source.
    Table 1 summarizes  the  PCB and
  lead  contaminant  concentrations
  measured  in  the  soil  from the
  composite of the grab  samples of feed
  taken during each  of the test runs. In
  addition to lead, where  concentrations
  ranged from 290  to  3000 ppm  and
  averaged  778  ppm,  several  other
  metals were  present  at average
  concentrations  exceeding 50  ppm
  including barium (591  ppm), zinc (301
  ppm),  and chromium  (85  ppm).  Total
  PCBs  concentration ranged from 10.2
  to 669 ppm and averaged 272 ppm.
    Several  samples  of  the   feed
  contained  small  quantities of TCDFs
  ranging from 0.04  to 0.1 ppb. Volatile
  and semivolatile organic  compounds
  including  methyl  ethyl  ketone,
  trichloroethene,  and  bis(2-ethyl-
  hexyl)phthalate were measured in feed
  samples at concentrations  less than 50
  ppm.  Methyl  ethyl  ketone  and
  trichloroethene were  also  detected in
  solvent blanks and are attributed to
  analytical laboratory contamination.

• Characteristics of the Furnace Ash

    Table 1  summarizes  the PCB  and
  lead  contaminant  concentrations
  measured in the furnace ash from the
  composited  grab samples  taken  at the
  conclusion of each test run. In addition
  to  lead, where concentrations ranged
  from 420  to  2000  ppm  and averaged
  1173 ppm, several other metals  were
  present at  average  concentrations
  exceeding  50 ppm including barium
  (1061  ppm),  zinc (410  ppm), and
  chromium  (81  ppm).  Total PCBs
  concentration ranged from  0.004 to
  3.396  ppm. Two samples  of furnace
  ash contained 0.07  and  0.3 ppb of
  TCDF  during two runs conducted at a
  900°F PCC  operating temperature; the
  normal PCC  operating temperature is
  1600°F.  These  runs  were   also
  conducted  without the input  of  PCC
  combustion  air  to   simulate   non-
  oxidizing  or  pyrolytic combustion
  conditions. The low PCC  temperature
  and pyrolytic environment could  have
  led  to the incomplete desorption  or
  incineration  of TCDF present in the
  feed or to  the production of TCDF from
  the incomplete combustion of PCBs in
  the feed. Volatile compounds including
  methylene  chloride,  methyl  ethyl
  ketone,  tetrachloroethene,  and
  trichloroethene were also measured in
  the furnace  ash   samples  in
  concentrations ranging from 3.9  to  64
  ppm with  one sample  containing 980
  ppm of methylene chloride. Methyl
  ethyl ketone  and trichloroethene  were
  also detected in  solvent  blanks and
  methylene  chloride is  commonly
  employed in laboratory procedures;
  therefore these compounds may  be

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Table 1.  Site Demonstration Test Results Summary
Operating Conditions
PCC
Temp.
"F
900a'b
900b
900b
1200
1200
7200<>
120Qb

1200»
7200*"
7400
7600
7600
7600
7600
7600
7600«
7600»
7600a«>

Residence
Time
min.
20
20
25
20
15
25
20

15
15
20
20
20
20
20
10
15
15C
15

PCB
ppm
327
20.2
367
297
27.6
456
669

602
309
56.0
10.2
35.2
20.4
t
391
451
271
311

Waste Feed
Characteristics
Pb
ppm
590
660
290
640
870
590
610

470
370
740
3000
1400
550
1100
620
620
390
500

EPTox
(Pb)
ppm
0.29
0.67
0.32
0.05
0.20
0.12
0.20

0.18
0.21
0.07
0.15
0.20
0.23
0.14
0.25
ND
0.53
0.07
3.009
TCLP
(Pb)
ppm
0.81
0.88
7.00
056
0.44
053
0.71

0.53
0.96
0.89
067
0.35
1.30
0.49
0.73
0.66
1.80
055
1.403
PCB
ppm
2079
3.396
0.168
0.115"
0.077
0.1081
0.066"

0.025"
0.066"
0.087"
0.037
0.772
0.003
I
0.045"
0.777"
0.004
0.067"

Furnace Ash
Characteristics
Pb
ppm
1,000
1,400
0.860
1,100
1,000
1,200
1.200

2,000
1,000
1,600
1,100
1,300
1,100
0.420
1,700
0.840
1,500
0.800

EPTox
(Pb)
ppm
0.38
0.89
0.88
4 10
0.38
0.14
0.06
4.909
h
046
ND
0.05
ND
0.13
028
ND
043
0.27
1.10

TCLP
(Pb)
ppm
2.90
620
3.80
1.60
3.60
005
4.10
2.809
h
0.82
0.15
ND
ND
0.05
1.80
1.00
0.17
0.23
2.40

* Waste feed blended with 3 wt.% fuel oil.
b Non-oxidizing atmosphere.
CPCC bed depth at 1 inch. All other tests at 7-7/2 inches.
dPCB levels below analytical detection limits. Total shown is sum of detectable limits indicated in analyses.
»ND - nondetectable value.
1 Run was conducted to make up for incomplete semivolatlle organics, PCDD/PCDF, soluble chromium and stack gas paniculate samplings on
 other runs.
9 Data from additional EP Tox and TCLP tests.
hND due to broken sample container.
  products  of  incomplete combustion
  and/or  the  result  of laboratory
  contamination.

  Residual PCBs in Furnace Ash
    During the demonstration test, a total
  of 17 runs were conducted at varying
  operating conditions. In addition to the
  ORE levels, which  are an indication of
  the performance of  the  Shirco  Pilot-
  Scale Infrared Incineration System and
  its ability to meet  RCRA and/or TSCA
  regulatory standards, the reduction of
  PCB concentration  from the feed to the
  furnace ash is  also a measure of the
  unit's  ability  to effectively  destroy
  PCBs and produce  a furnace ash with a
  PCB  concentration below the TSCA
  guidance level of 2  ppm.
    Based  on  the  data  presented  in
  Table  1, two samples  of furnace  ash
exceeded  the TSCA guidance  levels
and contained 3.396 and 2 079 ppm of
total residual  PCBs. The samples were
produced during two runs conducted at
a 900°F PCC  operating temperature
(20 minutes residence  time),  which is
significantly lower than the normal PCC
operating  temperature  of  1600°F.
These  runs  were also  conducted
without  the input of  PCC combustion
air  to  simulate  non-oxidizing   or
pyrolytic combustion conditions. At this
low  PCC  temperature and  pyrolytic
condition,  these higher total  residual
PCB levels in the furnace  ash may be
the result of the incomplete combustion
of PCBs in the feed.  This is  further
substantiated by the  residual  TCDF
present in  the  furnace ash  samples
from these same  two  runs,  as
discussed  previously.  The remaining
runs conducted  at 1200,  1400, ani
1600°F resulted in total residual  PCI
concentrations  in  the furnace as
ranging from 0.003 to 0.117  ppm. i
third run, which was  conducted  at
900°F  PCC operating temperature bi
with an increased PCC residence tim
of 25 minutes resulted in a total furnac
ash  PCB  concentration  of 0.168  ppr
with no detectable  TCDF.  It is possibl
that the increased residence time in th
PCC may  have  offset the low 900°
PCC  operating  temperature  an
provided the additional processing tim
for  the satisfactory destruction of th
PCBs in the feed.

Mobility of Heavy  Metals  - Feed an
Furnace Ash

  In order to determine whether heav
metals, particularly lead,  would leac

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  from the furnace ash produced in the
  Shirco Pilot-Scale Infrared Incineration
  System,  EP Tox and TCLP tests  were
  conducted to determine the mobility of
  heavy metals from the furnace ash as
  compared to the feed.
    The initial EP Tox analyses for lead
  in the leachate ranged  from 0.05 to
  0.67 ppm for the feed and 0.05 to 4.1
  ppm for the furnace ash.  The initial
  TCLP analyses ranged  from 0.35 to
  1.80 ppm (with one sample at 7.0 ppm)
  for the feed and 0.05 to  4.1 ppm  (with
  one sample at 6.2 ppm) for the furnace
  ash.
    A comparison of the  EP Tox  and
  TCLP analyses  conducted on  the
  furnace ash  and the feed do not show
  any trend or evidence  that  indicate
  reduced mobility  of lead from  the
  furnace ash versus the feed as a result
  of  the  thermal  treatment.  The
  comparison did  reveal  that   the
  concentrations  of  lead  in  the TCLP
  leachates from  both the feed and the
  furnace ash were  consistently higher
  than the corresponding  EP Tox  tests
  on the same samples.
    When several samples were retested
  to verify the results, the concentrations
  of lead in the  EP Tox leachates  (4.9
  ppm feed, 3.0 ppm furnace ash)  were
  higher than during the initial tests and,
  in direct reversal  to the original  data,
  exceeding  corresponding  TCLP
  leachate concentrations  (2.8 ppm feed,
  1.4  ppm furnace  ash).  The results of
  the  retest  again did  not indicate
  reduced mobility  of lead from  the
  furnace ash versus the feed as a result
  of the thermal treatment.
• Mobility of Heavy Metals - EP Tox and
  Proposed TCLP Toxicity Characteristic
  Standards
    EP Tox and TCLP tests  were  con-
  ducted on  the  feed,  furnace  ash,
  scrubber water, and scrubber solids. All
  of the results were below the EP Tox
  and   proposed  TCLP   toxicity
  characteristic  standards  of 5 ppm
  arsenic,  100  ppm  barium, 1 ppm
  cadmium, 5 ppm chromium, 5 ppm
  lead,  0.2  ppm  mercury, 1  ppm
  selenium, and 5 ppm silver except for
  one feed sample  at  7.0 ppm lead
  (TCLP ) and one furnace ash sample at
  6.2 ppm  lead (TCLP). A comparison of
  the EP Tox  and TCLP analyses on all
  the  sampled streams  to the  above
  mentioned standards do not show any
  trend or evidence that indicate reduced
  mobility of heavy metals as a result of
  the thermal treatment.
• Destruction and  Removal Efficiency
  (ORE) of PCBs

    The ORE of PCBs for the first three
  runs  (Phase I) is greater than 99.99%.
  In contrast, the regulatory  standard for
  incineration under the RCRA is 99.99%
  ORE  and under  TSCA is 99.9999%
  ORE. The low  PCB concentrations in
  the feed resulted in  PCB levels in the
  stack gas that were  less  than the
  analytical detection limits for two of the
  runs. Therefore for these  runs, ORE is
  calculated based on the  sum of the
  detection limits of the PCB congeners
  in order to  compare the  ORE for the
  runs  on the same  basis.  Stack gas
  measurements  conducted during the
  third  run did detect trichlorobiphenyl
  and tetrachlorobiphenyl congeners and
  a ORE is  shown  based  on  this
  measurement.  The less  rigorous
  sampling in Phase II of the test was not
  designed to allow calculation of ORE.

• Other Organic  Stack Gas and  PCC
  Offgas Emissions

    Several  volatile  and  semivolatile
  organic  compounds  were  detected in
  the stack gas  at concentrations  less
  than  100  ppb and  established
  standards  for direct inhalation.  Low
  levels of several phthalate compounds
  were  also detected  in  blank  samples
  and may be traced to contamination
  from  plastic  components in  the
  process, sampling equipment,  or
  laboratory apparatus. Several volatile
  organic compounds including  benzene
  and toluene were detected in the stack
  gas and  the scrubber makeup water
  and   may  be  attributable  to
  contamination from  the makeup water
  although PIC formation  is  a possibility.
  Other volatile and semivolatile organic
  compounds, which probably represent
  PICs, were detected.  They  include
  halomethanes,  chlorinated  species
  including   chlorobenzene  and
  methylene  chloride,  other  volatile
  organics including xylenes, styrene and
  ethylbenzene,  oxygenated hydro-
  carbons including acetone  and
  acrolem, carbon disulfide, and p-chlor-
  m-cresol. Dioxins and furans were not
  detected in the stack gas samples.
    The  majority  of  the  organic
  compounds present  in the PCC off gas
  samples at  levels less than 500  ppb
  were  also present in the stack gas. The
  additional destruction of organics that
  take place in the SCC and emissions
  scrubbing  system  reduced  the
  concentration  of  these  organic
  compounds in the corresponding stack
  gas samples.

• Acid Gas Removal

    During the  Phase I  Runs  1-3, HCI
  emissions  ranged from 0.181  to  0.998
  g/hr, which were significantly below the
  RCRA  performance  standard of 1800
  g/hr that would require a 99 wt.% HCI
  removal efficiency.  HCI  removal
  efficiencies ranged from 97.23 to 99.35
  wt.%.  Acid gas removal was not
  measured in Phase II.

• Particulate Emissions

    Particulate emissions were measured
  throughout the test and ranged from 7
  to 68 mg/dscm, well below the RCRA
  standard of 180 mg/dscm.

• Analysis of Scrubber Makeup Water,
  Scrubber Water, and Scrubber Solids

  Scrubber  makeup  water  was
transported to the site in a tank truck that
may  have contained  some  residual
contamination prior to fill  up. Samples  of
scrubber  makeup water were taken at the
end of each run.  No PCBs,  dioxins,
furans,   or  semivolatile  organic
compounds were  detected.  Several
volatile  organics  including benzene,
toluene,   and trichloroethene  were
measured at concentrations less than 15
ppm. The concentrations of heavy metals
were all less than 0.2 ppm.
  Samples of the  water  recirculation
through  the venturi scrubber  system,
referred to as scrubber water, were also
taken at  the end of each  run.  PCB
concentrations  were less  than  200 ppt
and no dioxins, furans, or semivolatile
organic compounds were detected. Small
quantities of  benzene  (2  ppm)  and
toluene (5.7 to 11  ppm) were measured
in   several of the samples  and are
attributable to the similar contaminants  in
the  scrubber  makeup  water.  The
concentrations  of  heavy  metals in the
scrubber  water were all less than 1 ppm
except for barium,  which ranged from 0.2
to 2.2 ppm, and lead, which ranged from
0.12 to 1.8 ppm.
  Insufficient quantities of scrubber solids
in the scrubber water were available for
analysis.

• Overall  Disposition of Metals

    Total  metals analyses  of the  feed,
  furnace ash, PCC offgas and stack gas
  particulates, scrubber makeup  water,
  scrubber water,  and scrubber  solids
  showed that the majority  of  the
  detectable  metals, including lead, that

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 entered the unit with the feed remained
 in the furnace ash.  An overall mass
 balance of lead through the unit  was
 calculated based on  the  analysis of
 lead in the samples, the measured feed
 rate  as  weighed during  the runs'
 operating  periods,  the  calculated
 furnace ash  flow rate based  on  the
 ultimate  analysis of  ash  in  the feed
 sample,  and  the measured particle
 mass and gas volume obtained from
 the gas' EPA Method 5 sampling trains.
 Phase I  results indicate an  average
 lead mass flow rate of 28.3 g/hr in the
 feed, 37.0 g/hr in  the furnace ash,
 0.206  g/hr  in the PCC  offgas
 particulates, and 0.109 g/hr in the stack
 gas particulates.  The quantity  of  lead
 leaving  the  unit  with scrubber water
 effluent is  approximately  0.204  g/hr
 based on  the  maximum  measured
 concentration  of  1.8 ppm  lead  in the
 scrubber  water and  an  overall
 approximate water flow rate of 30 gph.
 The PCC offgas particulates sampled
 during the Phase I  runs contained an
 average of  5364  ppm  of  lead  as
 compared to  stack  gas  particulates,
 which contained an average of  15,830
 ppm of lead. By contrast,  the average
 concentration  of lead in the feed  was
 1550 ppm. Although  the concentration
 of lead in  the particulate  matter
 increases  as   the  process  flow
 progresses through the unit, the actual
 mass flow of lead decreases as the gas
 stream  is cooled and treated  through
 the emissions control system.
   For the Phase I runs sampling  and
 analysis procedures were conducted to
 evaluate vaporous lead concentrations
 in the  PCC  offgas and  soluble
 chromium concentrations  in the PCC
 offgas and stack gas particulates.  The
 special sampling for vapor phase  lead
 and soluble chromium were unable to
 detect any of either metal at levels less
 than  2.7   ppb  and   264  ppb,
 respectively; therefore the  evaluations
 were inconclusive.
   Other heavy  metals,  particularly
 barium  and  zinc, with  average
 concentrations exceeding  100 ppm in
 the feed  (barium 591 ppm, zinc  301
 ppm) were  also  present  in high
 concentrations, relative to  other heavy
 metals, in the furnace ash (barium 1061
 ppm, zinc  410  ppm) and scrubber
 water (barium 0.8 ppm, zinc 0.3 ppm).

• Optimum Operating Conditions
   Phase II  was designed to examine
 the effect on  energy  consumption and
 changes in the residual levels of heavy
  metals and organics in the furnace ash
  versus the levels in the feed by varying
  operating conditions.
    Based on the  data  obtained  an
  analysis  was conducted to compare
  energy consumption in the  unit at
  operating conditions that did not affect
  the  performance  of  the  unit.  A
  reduction   in  the  PCC  operating
  temperature from  1600°F to  1200°F
  reduced the average  PCC power usage
  48%  from  0.2294 to 0.1200  kwhr/lb
  feed. A reduction in the SCC operating
  temperature from  2200°F to  1800°F
  reduced the average  propane  fuel
  consumption by  51%  from  3997 to
  1952 Btu/lb feed.  The  use of 3  wt.%
  fuel oil to supplement the fuel value of
  the feed further decreased PCC power
  usage by 26 to 67%  at PCC operating
  temperatures of 1600°F and 1200°F,
  respectively,  with  accompanying
  increases in overall feed rate  of 32%
  and 26%. The costs  for fuel oil and its
  attendant  facilities still must  be
  examined for  specific  applications to
  determine the cost effectiveness  of a
  fuel oil additive to the waste feed.
    As  discussed in previous  sections
  the results did not provide any trend or
  change in  the  residual  levels of the
  heavy metals  and  organics in the
  furnace ash versus  the  levels in the
  feed  as the operating conditions were
  varied and PCC  operating  temper-
  atures were maintained at 1200°F to
  1600°F.  At an  abnormally  low  PCC
  operating  temperature  of  900°F,
  without the  input of  combustion air to
  simulate  non-oxidizing  or  pyrolytic
  combustion conditions, total PCB and
  TCDF concentrations in the  furnace
  ash  increased.  The increases   may
  indicate that these PCC conditions led
  to incomplete desorption or incineration
  of PCB  and   TCDF  and   to  the
  production  of  TCDF from  the
  incomplete combustion of PCBs in the
  feed.

• QA Summary

    The Phase I  and II runs had a  well-
  defined quality  assurance/quality
  control  program  to   ensure  the
  collection  of  accurate  data.  This
  program was developed as part of the
  test program preparation activities and
  was formalized in the RREL approved
  QA Project Plan (Category II). All of the
  sampling  and  analytical  work  was
  conducted in accordance  with this QA
  Project Plan and the  results include
  data  quality credibility  statements and
  information that confirm the satisfactory
  precision and  accuracy of  the  date
  reported.

Conclusions
  Based  on  the  above  data  anc
discussion, the following conclusions car
be made  concerning the operation  anc
performance of the  Shirco  Pilot-Scale
Infrared Incineration System.

  I.The  PCC  equipped  with infrarec
    heating rods reduced PCBs from ar
    average of 272 ppm and a maximurr
    of 669 ppm in the feed to  less thar
    0.2  ppm  PCBs in  the  furnace  asr
    when  PCC temperature was 1200°F
    or higher. PCB levels in the ash were
    well below the TSCA guidance leve
    of  2  ppm  of PCBs in treatmen
    residuals.

  2. The majority  of the lead and othei
    heavy metals  present  in  the  feec
    remained  in the  furnace   ash
    regardless of operating  conditions
    However,  the  scrubber  wate
    contained levels of lead  and bariurr
    (up to 1.8 to 2.2 ppm, respectively)
    and  metals  also concentrated tc
    some extent in the furnace  ash. Bott
    residual streams  may require furthe
    treatment when metals are present ir
    the feed.

  3. In  most  cases  concentrations o
    metals in the extract of  the furnace
    ash did  not exceed  their respective
    EP  Tox and  TCLP  toxicity charac
    teristic standards.  The  need  fo
    further treatment of the furnace ast
    to reduce or immobilize the metals i:
    site specific, and will  depend on the
    cleanup standards for the site.

  4. Based on two leaching tests, the EF
    Tox and TCLP, the mobility of leac
    and other heavy metals  was simila
    in the feed and the furnace ash, anc
    there was no evidence that treatmen
    affected metals leaching.

  5. The  unit  achieved DREs  of  PCB;
    greater than 99.99%, based on one
    actual calculation and in  two  case;
    on detection  limits.  PCB concen
    trations in the feed  and  analytica
    detection limits  did  not allow th<
    demonstration  of 99.9999%  ORE
    required under TSCA. However, thi:
    unit achieved greater  than 99.99990/
    ORE in other tests, and  at this tim<
    at least one full-scale infrared system
    has  demonstrated  greater  thai
    99.9999%  ORE for  PCBs and i:
    permitted  under TSCA  to proces;
    PCB  waste.  The upcoming  Appli

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  cations  Analysis  Report
  incorporate this additional data.
will
6.The  unit  achieved  regulatory
  standards for acid  gas  removal and
  particulate  emissions.  These data
  apply to the  operation  and per-
  formance of the air pollution control
  system  installed  on  this  unit.
  Additional data on  the  performance
  of  air pollution control  systems  on
  full-scale Shirco Infrared units will be
  discussed in  the  Applications Anal-
  ysis Report.

7. Several semivolatile and  volatile
  organic compounds measured in the
  stack gas in the parts per billion may
  be  PICs.  These  levels are  much
  lower than established standards for
  direct inhalation of these compounds.

8. The unit was able  to reduce  the
  PCBs  in  the feed using less  power
                                                    when fuel oil was added to the waste
                                                    and  when  PCC  temperature was
                                                    reduced. The addition of fuel oil also
                                                    increased the feed rate. Cost savings
                                                    in specific  applications  will  depend
                                                    on local fuel and electrical costs, and
                                                    a minimum PCC  temperature must
                                                    be maintained  to  avoid inadequate
                                                    desorption of the organics in the feed
                                                    and the production of PICs.

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