PB84-167642
Decontamination of Hazardous Waste
Substances from Spills and Uncontrolled
Waste Sites by Radio Frequency in situ Heating
Rockwell International, Newbury Park, CA
Prepared for

Municipal Environmental Research Lab,
Cincinnati, OH
10B-1

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                                                    El'A-oOO/D-84-077
                                                                1984
           DECONTAMINATION OF HAZARDOUS WASTE
     SUBSTANv,r.S FROM SPILLS AI.'D UNCONTROLLED WASTE
        SITES BY RADIO FREQUENCY IN SITU HEATING
                           by

                       Harsh Dev
                    Jack E. Bridges
                   Guggi1 am C. Sresty
                 1IT Research Institute
                   Chicaoo, IL 60616
               Contract Number 68-03-3014
                    Project Officer

                    Hugh E. Masters
       Oil and Hazardous Materials Spills Branch
      Solid and Hazardous Waste Research Division
Municipal Environmental Research Laboratory (Cincinnati)
                Edison, New Jersey 08837
     'MUNICIPAL ENVIRONMENTAL RESEARCH
           OFFICE Or RESEARCH AND DEVt LOPJ-'.ENT
          U.S. ENVIRONMENTAL PROTECTION AGENCY
                 CINCINNATI , OHIO 45268

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                                   TECHNICAL REPORT DATA
                            (ftesie '>'oJ iHUmctiunt an i!if rct-ene be (ate ccmpl:iini>l
  EPA-600/D-84-C77
3. ftJCir-'ENT'S ACCCSSIOW NO,
    X' f LJ - / / '? *
    O /:• ^   / & / A-?
1. TITLE AND SUBTITLE
     Decontamination of Hazardous Waste  Substances
     From Spills and Uncontrolled Waste  Sites
     By  Radio Frequency in Situ Heating
5. REPORT DATE

  1331-
6 PERPOnMlNG ORGANIZATION CODE
                                                           8. PERFORMING onGAN.'ZATioN REPORT no.
    H. Oev,  J,  Bridges, G. Sresty
9- PERFORMING ORGANIZATION NAME AND ADDRESS
    Rockwell  International
    2421 West  Hillcrest Drive
    Newbury Park,  CA 91320
10. PBOGRA.M. ECtMSNT NO.

          C  B  R  D 1  A
V». CONTRACT/GRANT N07

          68-03-3014
12. SPONSORING AGENCY NAME ANO AOORtil
    Municipal  Environmental Research Laboratory—Cin; OH
    Office of  Research and Developmc-ntd
    U.S. Environmental Protection Agency
    Cincinnati,  OH 45268
                                                            13. TYPE OF REPORT AND PEH1OD COVERED
14. SPONSORING AGENCY CODE
          .1PA/QQQ/11
IS. SU(«PI.EMENTAfiY NOTtS
    Project officer:   Hugh'Masters (201)  321-6678
16. ABSTHACT
        The radio  frequency (Rf) heating process  can bo used to volumetrically
    heat and thus  decontaminate uncontrolled  landfills and hazardous  substances
    from^spil's.   After  the landfills are heated,  decontamination of  the  hajaroous
    substances_occurs  due to thermal decomposition,  vaporization, and distillation
    assisted with  steam  in a temperature range  of  3000 to 400°C in a  residence
    time of 14 days.   Heating is achieved by  laying  a row of horizontal conductors
    above the ground  surface of the landfill  and  exciting them with an RF
    generator through  a  matching ,  network.   This  method is particularly
    attractive for uncontrolled landfills since it does not require mining
    excavation, drilling,  or boring in the contaminated volume.

        Preliminary design and cost estimates were made for 3 mobile RF in  situ
    decontamination process.  Comparative cost  sudies indicate that the RF
    decontamination process is two  to four times cheaper than excavation of  the
    landfill and incineration  of the contaminated  volume in a nearby  incinerator.
    The economic attractiveness of  the process warrants laboratory verification of
    the decontamination  mechanisms  and field  studies.
                                Kt Y WORDS ANO DOCUMENT ANALYSIS
                  DISCMIPTORS
     i "(Bui ION.' :'. in t t.'.n:NT

           RELEASE TO PUBLIC



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                                                                         It, NO. Of PAGES
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Tliis document has been reviewed in accordance with
U.S. linvironmental Protection Agency policy and •
approved for publication.  Mention of trade names
or commercial products does not constitute endorse-
ment or recommendation for use.

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           DECONTAMINATION  0'  HAZARDOUS  HASTE  SUBSTANCES  FROM SPILLS



       AND UNCONTROLLED HASTE SITES BY RADIO FREQUENCY IN SITU HEATINGi








                                   Harsh  Oev



                               Jack  E.  Bridges



                              Guggilam C. Sresty



                            IIT Research Institute



                           Chicago, IPinois  60616








ABSTRACT




     The radio frequency (RF) heating process can be used to volumetrically



^e^t and thus decontaminate uncontrolled landfills and hazardous substances



from spills.  After the landfills are heated, decontamination of the organic




hazardous substances occur5 due to thermal  decomposition, vaporization, and



distillation assisted witr. steam in a temperature range of 300° to  40o°C in a



residence tine of 14 days.  Heating is achieved by laying a  row of  horizontal



co'nauctors above the ground surface of the landfill and exciting them with an



RF generator through a matching network.  This method is particularly attrac-



tive for uncontrolled landfills since it does not require mining, excavation,



drilling, or boring in the contaminated volume.
i.  This project has been supported with Federal funds from the U.S.



Environmental Protection Agency.  Work was performed'by IIT Research  Institute



as a subcontract under EPA contract No. 68-03-3014 with Rockwell  International



Corp.  Mention cf trade names or commercial products does not constitute



       m^nt or recommendation for use by the U.S. Government.

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     Preliminary design and cost estimates wore made  for a mobile RF  in situ




decontamination process.'  Comparative cost studies indicate that the  RF decon-



tamination process is two to four times cheaper than  excavation of the  land-




fill and incineration of the contaminated volume in a nearby incinerator.  The



economic attractiveness of the process warrants laboratory verification of the



decontamination mechanisms and field studies.








INTRODUCTION



     In the past century, technological advances leading to advanced  processes




and products have been accompanied by the generation  of unwanted waste



material.  Convenient but inadequate methods for disposing of these hazardous



wastes, often oy dumping or storing in landfills, have resulted in widely



publicized environmental pollution problems (Murray,  1979; Barnhart,  1979;



Maugh, 1979, 1979a; Chen, 1978).  Accidental spills during transport  of




hazardous materials have also contributed to the pollution problem.



     Hazardous waste materials have been improperly deposited in several



thousand sites a VI over the United States (Maugh, 1979).  Some of these




wastes, for instance the polychlorinated biphenyls (PCBs), are very stable anrl



can have serious detrimental effects on mankind and the environment.  The  U.S.



Environmental Protection Agency (EPA) has attemoted to correct the situation



by initiating various regulations that require better management of hazardous



waste disposal.



     Complete isolation or reclamation of these sites is preferred, but  the




cost and risk associated with site disturbance by available methods of  recla-



mation are considered prohibitive.  New treatment methods are needed  that  are




able to reduce the concentrations of hazardous substances to a level  where



they are harmless.  These methods should be cost effective and not give  rise

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:o (jroblems in oimr areas by transferring the substances  from one biosphere



to another.




     Tne radio frequency (RF) in situ heating process has  been demonstrated to



heat earth and mineral  formations rapidly to a temperature of 20'J°-600°C.   The



Hazardous substances present in a landfill can possibly be rendered harmless



by the application of the same in situ heating technology  at high tenperatures



(3UU°-4U'J°C) following relatively long soaking times  (up to two weeks).   The



process has the following potential advantages for landfill decontamination:



        • in situ treatment of most hazardous substances



        • no need for excavation, mining, earth-moving, or drilling



          activities on or through the contaminated volume



        • reduced exposure of operating personnel to  hazardous



          substances as opposed to other methods of cleanup




        • nobility of major capital equipment



        • riini.iiil environmental impact



        • snail amount of contaminated storage generated requiring



          special handling.








RADIO FREQUENCY KEATING TECHNOLOGY



     The term RF generally refers to  frequencies used in wireless communica-



tion.  The  frequencies can be as low  as 45 Hertz (Hz) or extend well  above



in ^igaHertz (GHz).  The frequencies  of principal interest to heat earth



resources are between 2 and 45 meyaHertz  (MHz).  Proper selection of  frequency



within this range will ensure electromagnetic wave penetration of a  few to




1U neters  into typical soil, while at the s&ie time generating average



absorbed power densities of about 0.3 v/atts per  kilogram (W/kg)  for  conserva-



tive values of electric field density. T|p   .liter-relationship between  soil

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properties aid selection of operating frequency is described elsewhere  (Von



Hipp»l, 19b-4; Bridges, et al., 1930).



Earlier dielectric heating designs



     Several types of electrical power input arrays  have been designed  and



tested for in situ heating of earth and mineral formations  (Bridges,  1980).



Most of these systems were designed for thermal resource recovery  from



deposits of oil shale, tar sand, heavy oil, etc.   Invariably, all  of  the



previous desiyns of RF energy input arrays consisted of electrodes, antennas,



or microwave exciters placed  in boreholes drilled  through the deposit.



     In principle, the previous dielectric heating methods  are  suitable for



true in situ volumetric heating of contaminated landfills,  but  require



drilling of boreholes through the contaminated  volume.  This creates  the



associated risk of contaminant redispersion, personnel exposure, and  fire  or



explosions from sparks during drilling activities.   It is therefore essential



to develop an RF energy applicator that is nonrcdiating and does not  require



drilling through the contaminated soil in order to neat uncontrolled  landfills



successfully.



Previous applications of the  RF process



     The radio frequency heating process has been  under development  since  the



nid-1970s for the recovery of hydrocarbons by  heating large volumes of  earth



In si tu.  After the initial laboratory experiments and the  development  of



computer models to predict the heating patterns based on deposit  properties,



fieid  experiments were conducted in  Utah.  The  first field  experiment was   ..



conducted at Avintaquin Canyon, where approximately  one ton of  oil shale  was



heated to about 38S°C (Carlson, 1980).  This was  followed by  two  field  experi-



ments  at the Asphalt. Ridge deposit of Utah.  Approximately  30  tons of tar  sand



were heated using RF energy and about 8 barrels of bitumen  were recovered  (30

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to 33% of the total  in place).  These field experiment-,  demonstrated that



large volumes of earth can be heated volunetrical ly to tenperatures of up to




400°C (Krstansky, 1982).  Background levels of the RF radiation in the



vicinity of the field test were monitored during the test.  It was found, that



leakaye radiation levels did not exceed the recommended ANSI Standard C-95.








IN SITU DECONTAMINATION WITH RF HRAT1NG



     The concept of in situ decontamination has three requirements:



     (1)  a hiyh temperature (300°-400°C) coupled with long residence




          times (1-2 weeks)                                                 ;



     (2)  the presence of decontamination mechanism(s) (e.g., thermal  ;     ;



          decomposition, distillation, vaporization, fixation to soil        '



          constituents) for the destruction or mobilization of the




          contaminants



     (3)  the presence of a gas and vapor recovery mechanism allowing :




          their collection at the surface.                               :



Decontamination mechanisms




     The ability of RF heating methods to heat large volumes of soils and




earth formations in situ rapidly can be applied to satisfy the first  require-



ment for the decontamination of soils containing hazardous chemical wastes.



     Thetiitel decomposition.  Temperature and residence time requirements  for



the thermal decomposition of chlorinated hydrocarbons (HCs) were estimated  by



extrapolating data obtained by Duvall (1930) for the incineration  of  hexa-



chlorobenzene (HCtf).  This approach was used to obtain preliminary engineering



estimates of the required tine and temperature in the absence of data for



thermal decomposition at low temperatures and  long residence  times.   Duvall's



data show that HCB can be 99.993% decomposed at 1000°C with a residence  tine



of 2 seconds (sec).




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     Based on tnese data, a rate constant of 1/2 sec"1, and an assumed



reasonable activation energy of 30 kcal/mole. the Arrenhius equation was used



to estimate time and temperature requirements.  At 344°C, the calculated



residence tine is 7 days for 99.993% decomposition of HCB.  In situ treatment



can easily provide such larye residence times economically because a costly



larye-volume reactor is not required.  Other decontamination mechanisms such



as vaporization, distillation, or stean distillation also help, in the recovery



of contaminants.  These can be collected at the surface of the landfill by an



appropriately designed vapor barrier and gas collection system.



     Distillation.  Many compounds found on the CERCLA Hazardous Substance



list are hydrocarbons (HC) boiliny between 80° and 420°C.  Heating these



compounds to 30'J0-4CO°C would recover a large fraction of the components by



vaporization and distillation.  Distillation is further assisted by the



presence of moisture in the landfill, since, in the presence of steam, the



boiliny point of the HC/water .mixtures is depressed.  This mechanism, however,



is effective only for those HCs with vapor pressures of the same order of



magnitude as water.



     In Table 1, the boiliny point reduction for some HCs in the presence of



water is compared with their normal boiliny points.  This table shows that



steam distillation can be performed with reasonable quantities cf stean, pro-



vided the vapor pressure of the component -is of the same order of magnitude as



that of water.



     For components boiliny at temperatures more than twice that of water,



steam distillation requires unreasonably larye quantities of saturated steam.



Such compounds, however, can be distilled in the presence of superheated



steam.  The  stean acts as a sweep gas that continuously carries the vapors

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away froio the surface where boiling  is  occurring,  ensuring  a  good  vaporization
rate.  The PCS mixtures o' the Aroclor  'anily, trichlorophenol,  and  benzidine
are examples of hazardous cnemicals  thst. can be  distilled with  superheated
steam.
     Prelininary estimates were made  for the anount  of  the  PCB,  Aroclor  1260,
that can be distilled witn superheated  steam generated  in situ.   This  calcula-
tion is based on equilibrium and thermcKiynairric considerations.   The  results
shown in Tjble 2 are based on the  following assumptions:  the landfill con-
tains 5 wti noisture, 25% of the total  moisture  present  in  the  landfill  gets
superheated to between  300° and 400°C,  approach  to equilibrium  is  only 25»,
and tne landfill area is  1 acre, depth  "-,  20 ft.
     The results in Table 2 show that,  with a  fixed  amount  of available
moisture, larger amounts  of Aroclor  12oO can be  distiller!  as  the temperature
is  increased.  Aroclor  1260 was selected in the  above  example as a worst case
since it na$ the highest  boiling range  (385°-420°C)  of the  PCB  family.
Vapor and gar. recovery  mechanism
     The RF power will  raise the temperature of  the  landfill  so that the
decontamination mechanism begins to  operate; the decontamination mechanisms
will thenselves decompose, pyrolyze,  distill,  and vaporize  the contaminants.
The vapor d;id gas recovery mechanisms will  allow the gases  to escape preferen-
tially towards the  landfill surface,  where tney  can  be collected for ultimate
disposal.
     The proposed RF exciter electrode  array will develop  a temperature  and
heating profile characterized by a penetrating phase change boundary at  wh'ich
water boils.  Figure  1  is a sketch G~  the  landfill showing  a  horizontal  dashed
Hne representing this  boundary.   T.h.-r  temperature above this  boundary will  be
hiijlier :.u.an  100°C,  and  the  temperature  below  it  less than  100°C.  In the
                            I'IT RESEARCH  INSTITUTE

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higher temperature region (Region A), the permeability of the soil to  flow of




gases and vapors will  be several fold gre-ter than the native pernec bi'. ity of




the landfill.  The permeability of the landfill wi 11  increase due to vaporiza-



tion of water and the  low boiling HCs present in the  pore space.



     The development of permeability will be directional because  it will De



confined to those regions where low boiling liquids have evaporated.   Thus the



region of high temperature, high permeability overlies the phase  change



boundary for water.  The str.an will become superheated as it moves towards the



surface through the hiyh temperature, high permeability zone of the landfill.



Un its way to the surface, the superheated steam will sweep the vapors of the



higher boiling components present 'in Region A.  The development of directional



permeability in tar sand formations was confirmed in  the laboratory and the



field by Krstansky and coworkers (1982).  Figure 2 illustrates  the increase  in



permeability of a tar  sand core above the boiling point of water.



     A vapor barrier placed above the heated landfill surface will confine and



collect the vapors rising to the surface.  These gases and vapors will be



treated for ultimate disposal by a combination of incineration  and on-site




treatment.



Process description



     A process flow sheet (Figure 3) was developed to allow cost  evaluation  of



the RF decontamination process.  A schematic cross sectional view of the land-



fill is shown in Figure 4.



     Rows of horizontal electrodes are placed a short distance  above  the




surface.  A vapor barrier is placed over the electrodes.  Collection  lines



carry the gases and vapors to a mobile treatment plant.  The vapor barrier  is



designed to operate under a slight vacuum to prevent  venting of the hazardous




gases and vapors to the environment.

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      The  impedance  matching  network,  RF  transnitters ,  and  other  RF  hardware



 (no:  snown)  are  placed  outside  tiie  vapor barrier.   Coaxial  cables carry  Rf



 power to  energize  individual  electrodes.  An  induced  draft  (ID)  fan carries



 the gases  through a gas  handling  system  consisting  of  a  gas/liquid  separator,



-condenser,  cooler,  and  another  gas/liquid separator.   The  outlet  o(r the  ID  fan



 discharges  to  a  demister.



      The  uncondensed yases  from the demister  outlet are  incinerated on  site  in



 a mobile  incinerator of  the  type  designed and built by EPA.   The  liquid  phase



 from  both  the  separators and  the  denister is  collected in  a  separator where



 the water-rich phase is  separated from the HC phases.  The  liquid KC phases



 are also  incinerated on  site.   The  water-rich phase is treated on site  to  pro-



 duce  process-quality w.ater  for  captive use in the plant.



      Other  alternative  process  designs are possible:   for  example,  on-site



 incineration of  all  the  gases and vapors without condensation, carbon adsorp-



 tion  instead of  incineration  of uncondensable gases,  or  treatment of liquid



 phases  at  off-site  locations.



 Treatment  duration



      The  time  required  to heat  a  landfill  1 acre in area and  20  feet (ft)  deep



 was calculated for  various  levels of  net power input  to  the  landfill and



 various temperatures between  300° and 400°C.   The duration  of treatrent  was



 calculated  by  adding a  soaking  time of 14 days to the  heat-up time.



      Figure  5  illustrates the relationship between  treatment  duration and  tem-



 perature.   Kor a net power  input  of 10 MW, the treatment time varies 60  to  90



 days  as temperature varies  from 300°  to  400°C.  For net  power inputs of  2  and



 5 MW, the  treatment tine increases  two-  to fivefold.   Based  on these calcula-



 tions,  a  net ;>ower  level  of  10  MK was selected for  cost  evaluation  purposes.



 An KF power  source  larger than  10 MW  is  required to account  for  power

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deposition inefficiencies.  These  include heat  loss  from the landfill, over-




heating, and transmission lire losses.




     Preliminary calculations on heat loss from the  landfill show that 15 to



21% of tne energy required to heat the landfill nay  be lost because of thermal



conduction.  This depends on the treatment duration  and the temperature.  An




overall deposition efficiency of 65.' was assumed.








PROCESS ECONOMICS



     Tne cost of landfill decontamination by in situ heating was developed by



separately estinatiny the capital and operating costs for tne process.   The



cost evaluation was based on the following:



        . Landfill  area is 4047 n2 (1 acre), depth is 6.1 m (20  ft).



        • Treatment temperature range is 300°  to 400°C.




        • Volatile matter in the landfill ranges between 5  to 20% by




          weight; 10% of the total volatile natter is organic.



        • Power will be provided by 10 2-MW RF  transmitters.



        • Other than the RF power source, all  other  process equip-



          ment are duplicated so that an average 2.6 sites  per year



          are treated by the single mobile RF  source.  This is



          possible because tno RF source is required at a site for




          only 60 to 90 days.  The remaininy part of the estimated



          9 months at each site is used  for installing and  taking



          down of equipment.




Capital cost



     The capital cost of the process was estimated by developing  the  cost of



each of the seven sub$ystens of the process separately (Table 3).   Vendor




quotations were used for all the r.ajor equipment items.  Estimates  were  based
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on two options:  purchased power and on-site power generation.  The capital




cost for purchased power is $17 million and 'or on-sif.e generation,




$27.5 Riilion.



Operating cost



     The operatiay costs of RF decontamination were calculated by separately




estimating the fixed costs for site preparation, equipment mobilization,



installation, tear down and decontamination, and permits and  licensing



requirenents (Table 4).  These costs are independent of treatment duration.



Variaole operatiny costs such as shift personnel salaries, par-diem payments,



electric power, water, fuel, and other consumable supplies were estimated  on a



daily basis.  The variable operating cost per day was multiplied by the



treatment duration and added to the fixed operating cost to obtain the  total



operating cost.



     Table 4 shows that the estimated  total operating cost varies  frcn  $3.2 to



54.2 million, depending upon the treatment  temperature and volatile natter



content.  If power is yenerated on  site, then the operating cost is higher by



45. to 54i.



Total cost of decontamination by the RF process



     The total cost of decontamination (Table 5} varies between $4.6  to



$5.7 million per site.  If power is yenerated on site, then the total treat-



ment cost is higher by 49 to 55%.



     Tne total decontar.ination cost was obtained by addin-j depreciation and



interest to the operatiny cost.  A  uniform  straight line depreciation was



assumed, with an average interest rate of  22.0% per year.



Cost of decontamination by the incineration process



      In the incineration process all the contaminated soil and drums  of



hazardous substances are excavated  from the landfill and  shipped  to tin  Annex  1
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incinerator.  7no  drums  are  separately  recovered  and  the  waste  liquids are



transferred  to  bul.<  liquid  tankers.   The  soil  is  loaded  in  sealed roll-off.



boxes  for  shipment.



     Our calculations were  Marie  on  the  assumption that  an Annex 1 incinerator



was  available within  250 to  500  miles of  the  landfill.   The incineration cost



-was  assumed  to  vary  between  6  and  16<|/lb.



     The operating cost  of  treatment  by excavation and  incineration (Table 6)




varies  between  $8.9  to  $25.1 million  depending upon the  volatile natter




content, distance  to  the incinerator, and  the incineration  cost.  This estimate



does not include depreciation  and  interest on capital  cost.  The interest and



depreciation were  calculated  in  a manner  similar  to that  of the RF process, and



are  included in Taole 7.



     The total  treatme.it cost  for  incineration (Table 7)  varies between $9.0




and  $25.2  million  per site.  The single largest, cost  component  in this estimate



is t.ne  incineration  cost, which  constitutes 79 to 84% of  the operating cost.



The  capital  cost for  the incineration process (Table  8)  "is  estimated at




$0.83  million.








RESULTS AND  CONCLUSIONS




     A  comparison  of  the costs of  decontaminating a hazardous substance land-



fill by RF in situ heating  and by  incineration (Table 9)  indicates that the RF



in situ process  is 2  to  4 times  cheaper than  incineration.




     The KF  process  also offers  significant safety and  environmentdl advantages:



        •  in situ  treatment  of the  hazardous  substances



        •  safe  containment  of  the  hazardous waste



        •  reduced  exposure  of  operating personnel to  hazardous



           substances
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        • only a sn?ll amount o',: the contaminated waste tonnage



          generated nay require special handling.




     Tne incineration process has alreedy been demonstrated  to decontaminate  a




wide spectrum of wastes found buried in landfills.  However,  large-scale



incineration of contaminated soils may not be  iimmediately  feasible due  to  the



inadequate installed capacity of Annex 1  incinerator.




     The technical  feasibility of the various  proposed decontamination  mechan-



isms proposed for the RF process should be verified in laboratory  studies.








ACKNOWLEDGMENTS



     The authors g.acefully  acknowledge the  assistance and  encouragement



provided by ,".r. Frank Freestone and Mr. Hugh Masters, U.S.  Environmental



Protection Agency, OHMS Branch, and Dr. Walter Unterberg,  Rockwell




International, EMS Center.   The work reported  herein was  submitted to  Rockwell



International in fulfillment of Contract  68-03-3014 under  the sponsorship  of



the U.S. Environmental Protection Agency.








REFERENCES



 1.  Barnhart, Benjamin J.,  1979.  The disposal  of hazardous wastes.




     Environmental  Science and Technology.



 2.  Bridges, J., et al.,  1980.  Radio frequency heating  to  recover  oil  from



     Utah tar sand.  Future  of Heavy Crude and Tar Sands,  McGraw Hill,  1980,




     pp. 396-409.



 3.  Carlson, R. D., E. F. Blase, and T.  R.  McLendon,  1981.   Development  of



     the IIT Research  Institute RF heating process for in  si tu  oil  shale/tar




     sand fu-al extraction-an overview.  Proceedings of the  14th  Oil  Shale



     Synuasiur-i.  Colorado  School of Mines, Golden, Colorado.

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 4.   Chen, T.  T., M. Chen, and J.  lauber, 1973.  Incineration of toxic




     chemical  wastes.  Pollution r'niji
 5.   Duvall, D. C., W. A. Rt-Dey, and. J. A. Kescher, 1980.  High-tenperature



     decomposition of organic hazardous waste.  Disposal of Hazardous Waste,




     Sixth Annual  Research Symposium, D. Schultz, Ed., Chicago, EPA 600/9-80-



     010.   ppl21-131.



 6.   Krstansky, J., et al., 1982.  RF Heating ' Q* Carbonaceous Deposits.  DOE



     Report DOE/ER/10181-1, IIT Research Institute, Chicago.



 7.   Maugh, Thomas H. , 11, 1979.  Toxic waste disposal, a growing problem.



     Science.



 8.   Mauyh, Thomas H. , II, 1979a.  Hazardous wastes technology is available.




     Sc ience.



 9.   Murray, Chris, 1979.  Chemical  waste disposal, a costly problem.



     Cherr.ical and  Engineering News.



10.   Von Hippel, A. R., Ed.,  1954.  Dielectric Materials and Applications.



     John  Wiley and Sons, New York.

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                                LIST OF TABLES








Table 1.  Boiliny Point  Reduction  and  ideal  Stean Requirements for Steam




          Ui sti1lation.



Table 2.  Temperature Required  for  Superheated-Stean Distillation of



          Aroclor 1260



Table 3.  Summary of Capital  Equipment Costs  for  the RF  Process



Tabl'e 4.  Total Operating  Cost  Per  Site for  the  RF  Process  [Purchased Power



          Option]



Table 5.  Treatment Cost  for  Decontamination  of  Hazardous  Waste Landfills by



          the  RF Process  (Including 10£ Contingency for  Operating Costs)




          [Purchased Power  Option]



Table 6.  Total Operating  Costs  Per Site  for  the  Incineration Process




          (Includes 10%  Contingency Allowance)



Table. 7.  Treatment Costs  for Decontamination of  Hazardous  Waste Landfill by



          the  Incineration  Process



•Table 8..  Cost  of Capital  Equipment Required  for  the Incineration Process



Taole 9.  Comparison ct7  Decontamination Costs for the RF and Incineration




          I'rocesses
                                      15

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Component
Benzene
Toluene
Bromoforn
Chlorobenzene
Hexachloroethane
Mixture
Boi 1 iny Temp. ,
°C
68.3
83.9
94.3
91.0
98.7
Pure Component
Boiling Point,
°C
80.1
110.6
150.0
112.5
186.0

Ib Stean/
Ib Component
0.092
0.236
0.311
0.405
1.57
16

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 "r, Aroclor



in Landfill




    Mass
    Weight of



Aroc'ior Distilled,




    Ib (xlO6)
Mass Steai-i/



Ib Aroclor
 Requi red



Temperature,




    °C
    1.1



    5.8



   26.0
      1.43



      7.7



     35. U
   1.13



   0.21



   0.04
    300




    350



    375
                                       17

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                                                              Total



                                                             Quantity     Cost,



              Subsystem Description                          Required    S  x  106







1U, 2-MW RF transmitters, transmission cables,                  1        13.33



  matchiny network, and dummy load



Vapor barrier and 
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                               Cost (S x 106)
 Volatile      	Temperature, °C	



Matter, %      300      325      350       375      400








    20          3.86     3.96     4.03      4.10     4.21



    10          3.40     3.51     3.61      3.72     3.82



     5          3.15     3.26     3.36      3.47     3.56
                              19

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                          Cost (S x 106)
 Volatile             Treatment Temperature,  °C
Matter, %     300       325.  .   350       375      400








    20         5.34      5.44     5.51      5.58     5,69



    10         4.83      4.99  , -  5.09      5.20     5.30



     5         4.63      4.74.V    4,84      4.95     5.04
                           20

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                                   Cost Per  Site at  (S  x  10
Volatile            403 km to Incinerator                803 !
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                                     Cost Per Site  (S  x  106)
Volatile            400  kn  to  Incinerator               80fi  kn  to  Incinerator
                                       22
."latter, %            6
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                Description
Total



Quantity      Cost,  £
Bulldozer with a ripper




Front end loader with a backhoe



Roll-off boxes with gasketted-hinged doors



Decontamination showers on a mobile trailer



Trailer mounted mobile laboratory



Mooile diesel generator set, 75 kW



Monitoring equipment




Ualkie-talkie radios



Total cost of capital equipment
    2



  300
320,000



160,000



153,000



 40,000



100,000




 28,000



 24,000



  7,000



832.000
                                   23

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                     RF Process*
Incineration Process'*"*
Volatile
Matter, %
20
10
5
'•-
S x 106/Site
5.34-5.69
4.88-5.30
4.63-5.04
S/100 Ib.
Material
4.97-5.30
4.00-4.34
3.53-3.84

S x 106/Site
9.0-21.5
9.7-23.9
10.2-25.2
S/100 lb
Material
8.4-20.08
7.96-19.61
7.79-19.26
* Temperature range:  300°-400°C



**lncineration cost range:  6.0f/lb-16.0
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                             '.  LIST OF FIGURES








Fiyure 1.  Temperature profile and development of  permeability



Figure 2.  Permeability development curing heating of mineral  resources



Figure 3,  Cross section of the KF energy input  array and  the  vapor  harrier



Fiyure 4.  Preliminary process flow Ciayrarn for  decontamination  of  landfills



Figure 5.  Treatment duration as a function of treatment temperature

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                    VAPORS RECOVERED
                    FROM THIS SURFACE
o
            ABOVE IOO"C
          HIGH PERMEABILITY
              (REGION A)
               BELOW lwO°C
             LOW PERMEABILITY
                (REGION B)
        MOVING PHASE CHANGE BOUNDARY
              WATER BOILS HERE
  z
  UJ
  o
  o
  o:
  ten
    700^

    600

    500

zo 400
— 
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BAFFLES FOR
CO.NDtNSATE
COLLECTION
              \
                                          GAS COLLECTION
                                             DUCTWORK
                                                  RFGROUND
                                                 PLANE WIRE
                                                     MESH
                                                    .VAPOR BARRIER
                                                    CONCRETE
                                                    / SUPPORT
EXCITER ELECTRODE
\
ALUMINA ELECTRODE
     SUPPORT

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TO ONSITE
VAPOR BARRIFR
VAPOR AND GAS COLLECTIO
1,11 1
I 0
inn H P li i
TREATED
VOLUME
	 .,— — if 	 • —

_JL^.
X
TREATED / . \
TnWFR COOLING
TOWER VVATER
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r< >-
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SEPARATOR
I-
WITH EPA MOBIL Ef
INCINERATOR 4

.^—^'IILU DE MISTER
r~~*Q _,
i 1.0,
] FAN
GAS /LIQUID
SEPARATOR
i
LIQUID CONDENSATE -JLJ-jL, ,
L.IWUIU uwrauc.ix3Mi c. -*-*-A~ LIQUID /LIQUID
-«™^«i ..,.--« cc"fv\ r> ATH Q
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PH i-
ADJUSTMENT
_JL_ y-1
j WATER
^^l^^ ^»* PHASE
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IS* 3
K# l-:


UGHT^ANiC TOIMCINESATIW
PHASE PUMP
/• ™\: "^
WATER l" PRESSURE W
pp£5«rc* 	 CAR80N F'LT£R HEW-ORGANIC' '.
PfP.hr,, o ADSORPTION PHASE PUMP
M AKt Ur

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 500i

 400
300
                        VOLATILE
                         WAITER
                          •20%


                          5%
150
                         •20%

                         10%
                                              5,0 MW
70
60
        300
325
                       350    375

                  TEMPERATURE t
                      400
                              10.0 MW

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