United States
            Environmental Protection
            Agency
            Office of Research and
            Development
            Washington DC 20460
EPA/540/A5-89/012
September 1990
&EPA
Ultrox International
Ultraviolet
Radiation/Oxidation
Technology

Applications Analysis Report
                  SUPERFUND INNOVATIVE
                  TECHNOLOGY EVALUATION

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                                    EPA/540/A5-89/012
                                     September 1990
 Ultrox International Ultraviolet
Radiation/Oxidation Technology

   Applications Analysis Report
        Risk Reduction Engineering Laboratory
         Office of Research and Development
        U.S. Environmental Protection Agency
              Cincinnati, OH 45268

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                                  Notice
The information in this document has been funded by the U.S. Environmental
Protection Agency under the auspices of the Superfund Innovative Technology
Evaluation (SITE) program (Contract No. 68-03-3484). It has been subjected to the
Agency's peer and administrative review and it has been approved for publication.
Mention of trade names or commercial products does not constitute an endorsement or
recommendation for use.
                                     11

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                                 Foreword
The Superfund Innovative Technology Evaluation (SITE) Program was authorized in
the 1986 Superfund Amendments and Reauthorization Act (SARA). The program is a
joint effort between EPA's Office of Research and .Development (ORD) and Office of
Solid Waste and Emergency Response (OSWER). The purpose of the program  is to
assist the development of hazardous  waste treatment technologies necessary to
implement new cleanup standards which require greater reliance on permanent
remedies. This is accomplished through  technology  demonstrations which are
designed to provide engineering and cost data on selected technologies.

This project is a field demonstration under the  SITE Program and is designed to
analyze Ultrox International's ultraviolet radiation/oxidation technology.  The
technology demonstration took place at a former drum recycling facility in San Jose,
California. The demonstration effort was directed to obtain information on the
performance and  cost of the technology and to assess its use at this and other
uncontrolled hazardous waste sites. Documentation consists of two reports: (1) a
Technology Evaluation Report that describes the  field activities and laboratory
results; and (2) this Applications Analysis Report that provides an interpretation of
the data and discusses the potential applicability of the technology.

A limited number of copies of this report will be available at no charge from EPA's
Center for Environmental Research Information, 26 Martin  Luther King Drive,
Cincinnati, Ohio 45268. Requests should include the  EPA document number found on
the report's cover. When the limited supply is exhausted, additional copies can be
purchased from the National Technical Information Service, Ravensworth Building,
Springfield, Virginia 22161, (703) 487-4600. Reference copies will be available at  EPA
libraries in the Hazardous Waste Collection. You can also call the SITE Clearinghouse
hotline at (800) 424-9346 or (202) 382-3000 in Washington,  D.C., to inquire about the
availability of other reports.
E. Timothy Oppelt, Director
Risk Reduction Engineering Laboratory
                                     111

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                                  Abstract
In support of the U.S. Environmental  Protection Agency's (EPA) Superfund
Innovative Technology Evaluation (SITE) Program, this report evaluates the Ultrox
International technology and its applicability as an  on-site treatment method for
contaminated groundwater. The ULTROX® technology (a registered trademark of
Ultrox International) simultaneously uses ultraviolet (UV) radiation, ozone, and
hydrogen peroxide to oxidize dissolved organic contaminants (subject of a U.S. patent),
including chlorinated hydrocarbons and aromatic compounds, found in groundwater or
wastewater. This report evaluates both treatment efficiency and economic data from
the SITE demonstration and seven case studies.

Under the SITE Program, the ULTROX® technology demonstration was conducted at
the Lorentz Barrel and  Drum (LB&D) site, San Jose, California, in February and
March of 1989. During  this demonstration,  the Ultrox  system achieved volatile
organic compound (VOC) removals greater than 90 percent. The majority  of VOCs
were removed through  chemical oxidation.  However, stripping also  contributed
toward removal of a few VOCs, such as 1,1,1- trichloroethane (1,1,1-TCA) and 1,1-
dichloroethane (1,1-DCA). The treated groundwater met the applicable National
Pollutant Discharge Elimination System (NPDES) standards for discharge into a local
waterway. In addition, there were no harmful air emissions to the atmosphere from
the Ultrox system, which is equipped with an off-gas treatment unit.

The results from seven case studies are also summarized in this report. Six of the seven
case studies involved facilities that were  primarily contaminated with VOCs and
polychlorinated biphenyls, in the ppm and ppb concentration ranges. The other case
study involved a wood treatment facility contaminated with phenol at 150 to 200 mg/L
and pentachlorophenol  at 1 mg/L. In all the  case studies, effluent from the Ultrox
system met the applicable discharge standards.  Pretreatment was required for
influent that contained high levels of manganese, oil and grease, and suspended solids.

Potential sites for applying this  technology to contaminated groundwater include
facilities with sources of petroleum, wood treatment facilities,  and facilities with
sources of chlorinated or nonchlorinated solvents.  Economic data indicate that the
capital costs for the reactor and ozone generator would range between $70,000 to
approximately $260,000. Operation and maintenance costs can be as low as $0.25 per
1,000 gallons treated, considering only oxidant and electrical costs, or exceed $17 per
1,000 gallons treated, if extensive pretreatment is required.
                                      IV

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                                  Contents
                                                                        Page
Foreword	 iii

Abstract  	 iv

Figures	  vii

Tables	  vii

Acknowledgments	  viii
    1. Executive Summary  	  1
      Introduction	  1
      Overview of the SITE Demonstration	  1
      Results from the SITE Demonstration  		  1
      Results from the Case Studies	  2
      Waste Applicability 	  2
      Economics  	  3

    2. Introduction 	  5
      Purpose, History, and Goals of the SITE Program	   5
      Documentation of the SITE Demonstration Results  	   5
      Purpose of the Applications Analysis Report  	   6
      Technology Description	  6

    3. Technology Applications Analysis	,	  9
      Introduction 	  9
      Technology Evaluation  	  9
      Site Characteristics	  13
      Materials Handling Required by the Technology  	   14
      Personnel Requirements	  15
      Potential Community Exposures  	  16
      Regulatory Requirements 	  16

    4. Economic Analysis  	  21
      Introduction	  21
      Site-Specific Factors Affecting Cost 	  21
      Basis of Economic Analysis  	  21

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                         Contents (Continued)
References  	  25

Appendices	  27

   A. Key Contacts for the SITE Demonstration  	  27
      The Ultrox Technology  	  29
      The SITE Program 	  29
      The Demonstration Site  	  29

   B. Vendor's Claims for the Technology 	  31
      Introduction 	  34
      Description of the ULTROX® Process  	  34
      ULTROX® Equipment 	  35
      Applications of the ULTROX® System  	  35
      Selected Case Studies	*	  39
      Cost Information  	  40
      Summary  	  40

   C. SITE Demonstration Results  	  43
      Introduction 	,	  46
      Site Characteristics 	  46
      Waste Characteristics 	  47
      Review of Technology and Equipment Performance	  48
      Review of Treatment Results  	  51
      References  	  53

   D. Case Studies	  55
      Introduction	  58
      D-l Department of Energy, Kansas City Plant, Missouri  	  58
      D-2 Hewlett Packard Facility, Palo Alto, California  	  60
      D-3 FBI Microwave, Sunnyvale, California  	  63
      D-4 Golf Course, City of South Gate, California   	  65
      D-5 Xerox Facility, Webster, New York	  66
      D-6 Koppers Industries, Denver, Colorado  	  68
      D-7 General Electric Company, Lanesboro, Massachusetts  		  69
      References	  69
                                     VI

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                                  Figures
Number
   2-1
   3-1
Isometric view of the Ultrox System	
Dye tests showing effects of gas flow rates on the mixing
characteristics of a bubble diffuser ozone contact basin .
Page
.   7

  12
                                 Tables
   2-1     Comparison of Technologies for Treating VOCs in Water  ..
   4-1     Estimated Costs Associated with Three Ultrox System Units
                                                              8
                                                             21
                                    VII

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                          Acknowledgments
This report was prepared under the direction and coordination of Norma Lewis, U.S.
Environmental Protection Agency (EPA) Superfund Innovative Technology
Evaluation (SITE) Project Manager in the Risk Reduction Engineering Laboratory,
Cincinnati, Ohio. Mr. David Fletcher, Ultrox International, contributed greatly to this
report. Many other individuals provided information useful in summarizing the case
studies.

Dr. Gary Welshans, Dr. Kirankumar Topudurti, Barbara  Sootkoos, and Sharon
Weinberg of PRC Environmental Management, Inc., prepared this report for EPA's
SITE Program under Contract No. 68-03-3484.
                                    viu

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                                          Section  1
                                    Executive Summary
Introduction
The Ultrox International ultraviolet (UV)
radiation/oxidation technology (ULTROX®, a
registered trademark of Ultrox International) was
evaluated under the U. S. Environmental Protection
Agency's (EPA) Superfund Innovative Technology
Evaluation (SITE) Program. The Ultrox technology
demonstration was conducted at the Lorentz Barrel
and Drum (LB&D) site in San Jose, California,
during February and March of 1989. The Ultrox
treatment process (U.S. Patent No. 4,792,407) uses a
combination  of UV radiation, ozone,  and hydrogen
peroxide to oxidize organic compounds in water. The
developer claims that the final reaction products are
salts, water, carbon dioxide, and possibly some
organic acids.

The technology demonstration had the following four
objectives: ,

1.  Evaluate the technology's ability to treat organic
   contaminants in the groundwater at the site

2.  Evaluate the effects of major process parameters
   on the technology's performance
3.  Evaluate the efficiency  of the ozone decomposer
   (Decompozon) unit in treating ozone in the off-gas
   from the Ultrox reactor

4.  Develop  information  useful  for evaluating
   whether  this technology is suitable for other
   hazardous waste sites with similar conditions

The purpose of this report is to provide information,
based on the results from the SITE demonstration
and other case studies, necessary for implementing
the Ultrox technology at Superfund  and Resource
Conservation and Recovery Act (RCRA) hazardous
waste sites. Section 2 presents an  overview of the
SITE Program and a description of the Ultrox
technology. Information relevant to the technology's
application, including pre- and  post-treatment
requirements, operation and maintenance
requirements, potential  community exposures, and
environmental regulations are presented in Section
3.  Section 4 summarizes the costs  associated with
implementing the  technology.  A list of contacts
familiar with the demonstration, the vendor's claims
regarding the technology's performance, a summary
of the SITE demonstration results; and seven case
studies are included in Appendices A  through D,
respectively.

Overview of the Site Demonstration

The shallow groundwater at the LB&D site was
selected as the waste stream to be used for evaluating
the Ultrox treatment process. This groundwater was
primarily contaminated with  volatile organic
compounds (VOC) such as trichlproethylene (TCE)
and vinyl chloride, at  levels of  100 and 40 ug/L,
respectively. Other VOCs present at relatively low
concentrations (in the range of 5 to 15 ug/L) included
1,1-dichloroethane (1,1-DCA), 1,1,1- trichloroethane
(1,1,1-TCA), 1,2-dichloroethane (1,2-DCA), benzene,
chloroform, and tetrachloroethylene. Semivolatiles
and polychlorinated biphenyls (PCB)/pesticides were
not detected.

The total organic carbon (TOG) concentration of the
groundwater was approximately 25 mg/L. However,
the concentration of priority pollutants  (VOCs and
semivolatiles) was only 2 percent of the TOG
concentration.

The pH and alkalinity of the groundwater were about
7.2 and 950 mg/L  as CaCOs, respectively. These
measurements indicated that the bicarbonate ion
(HCOs"),  which acts as  an oxidant scavenger, was
present at high levels. Other oxidant scavengers such
as bromide, cyanide, and sulfide were not detected.

The experimental demonstration program evaluated
the performance  of the Ultrox technology  in
removing VOCs from the groundwater under various
operating conditions. During the demonstration
program, hydraulic retention times, oxidant doses
and ratios, UV radiation intensities, and  influent pH
levels were varied for each test. The Ultrox system
was shut down at the end of each test and was not
started up until the next  test.


Results from the Site Demonstration
The groundwater treated by the Ultrox system met
the applicable  National Pollutant  Discharge

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Elimination System (NPDES)  standards for
discharge into a local waterway under certain
operating conditions. The Ultrox system achieved
removal efficiencies as high as 90 percent for the total
VOCs present in the groundwater. The removal
efficiencies for TCE were  greater than 99 percent.
The maximum removal efficiencies for 1,1-DCA and
1,1,1-TCA under optimal operating conditions were
about 65 and 85 percent, respectively.

One set of operating conditions included a hydraulic
retention time of 40 minutes, ozone dose of 110 mg/L,
hydrogen peroxide dose of 13 mg/L, all 24 UV lamps
(at 65 watts each) operating, and influent pH of 7.2
(unadjusted). These "preferred" parameters were
selected for verification of subsequent runs during
the demonstration based on achieving acceptable
effluent at the lowest operating cost.

Within the treatment system, the  removals of 1,1-
DCA  and 1,1,1-TCA appear  to be  due to both
chemical  oxidation and stripping.  Specifically,
stripping accounted for 12 to 75 percent of the total
removals for 1,1,1-TCA, and for 5 to 44 percent of the
total removals for 1,1-DCA. However, stripping
accounted for less than  10 percent of the total
removals for TCE and vinyl chloride. For other VOCs
such as 1,1-dichloroethylene, 1,2-dichloroethylene,
benzene, acetone, and  1,1,2,2-tetrachloroethane,
stripping was negligible. Volatile organics present in
the gas phase within the  reactor  at levels  of
approximately 0.1 to 0.5 ppm were removed to below
detection levels in the Decompozon unit.

The Decompozon unit destroyed ozone in the Ultrox
reactor off-gas  to levels  less than 0.1 ppm
(Occupational Safety  and  Health  Act (OSHA)
standards). The ozone destruction  efficiencies were
observed to be greater than 99.99 percent.

Based on the gas chromatography (GC) and GC and
mass spectrometry (MS) analyses performed for
VOCs, semivolatile organics, and PCBs/pesticides, no
new compounds were detected in the effluent.  In
addition,  very low TOG  removal occurred.  Since
VOCs made  up less than 2 percent of the  TOC,
complete conversion of VOCs to carbon dioxide and
water could not be verified.

The Ultrox  system's average electrical energy
consumption  was about  11  kilowatt-hours/hour of
operation.

Results from the Case Studies
Information on the Ultrox technology's performance
at seven facilities was evaluated to provide additional
performance data. These facilities were:

1.  The Department of Energy, Kansas  City,
    Missouri
2.  Hewlett Packard, Palo Alto, California
3.  FBI Microwave, Sunnyvale, California
4.  Golf Course, City of South Gate, California
5.  Xerox, Webster, New York
6.  General  Electric  Company, Lanesboro,
   Massachusetts
7.  Koppers Industries, Denver, Colorado

Groundwater  treated  by the Ultrox  system at
Facilities 1 through 6 was generally contaminated
with several VOCs, including vinyl chloride, TCE,
benzene, toluene, xylene, tetrachloroethylene,
methylene chloride, 1,1-DCA, and 1,1,1-TCA, and
PCBs. The contaminant  concentrations in the
influent were in both the ppb and ppm ranges. The
effluent from the Ultrox system was able to meet the
discharge standards  in all cases, with treatment
efficiencies ranging from 90 to 99.99 percent in most
of the cases. The removal efficiencies for 1,1-DCA arid
1,1,1-TCA were less than 40 percent.

At  Facility  7,  wood treatment wastewater
contaminated  with phenols,  pentachlorophenols
(PCP), and oil  and grease was treated by the Ultrox
system. Phenol was present at 150 to 200 mg/L, PCPs
at 1 mg/L, and oil and grease at 3 percent in the
influent. The effluent from the Ultrox unit met the
applicable discharge standards.

Pretreatment  was required for cases where the
influent contained high levels of iron, manganese, oil
and grease, or suspended solids.  Pretreatment
included precipitation of iron and  manganese
followed by filtration,  breaking of the oil-water
emulsion,  and removal of suspended solids by
filtration.

Operational problems were encountered at Facility 1,
which resulted in frequent shutdowns of the Ultrox
system. Some operational  problems included
frequent cleaning of UV lamps and ozone  spargers,
and the  ultimate replacement  of ozone spargers.
These problems were due to the precipitation of iron
and manganese within the reactor. The facility also
reported  the  following additional operational
problems: (1) air compressor systems do not yield air
that is adequately dry; (2) ozone generator has  a
highly variable ozone output; and (3) the unit suffers
from poor transfer of ozone from the gas  to liquid
phase.

Waste Applicability
This technology can be applied to groundwater and
industrial wastewater contaminated  with VOCs,
semivolatiles,  and PCBs/pesticides. Potential  sites
for  applying  this technology  to  contaminated
groundwater  include  facilities with sources  of
petroleum, wood treatment facilities, semiconductor

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manufacturing facilities, and other facilities with
sources of chlorinated or nonchlorinated solvents.
Economics
An economic analysis was performed which
examined 12 separate  cost categories for three
treatment flow rates (20, 100, and 250 gpm). This
analysis assumed that the system would operate in a
continuous mode (24 hours a day, 7 days a week) for
one year. The economic analysis was carried out for
one year to provide a reliable estimate of annual
operation and maintenance (O&M) costs. Annual
O&M costs were estimated to be $63,100, $135,100,
and $240,400 for the 20-, 100-,  and 250-gpm units,
respectively. Capital costs for these reactors ranged
from $70,000 for the smallest unit to $260,000 for the
largest. O&M costs are presented in the appendices
for several operating or demonstration systems. The
costs from the case studies presented in Appendix D
ranged from approximately $0.25 per 1,000 gallons of
treated  wastewater, considering only oxidant and
energy costs,  to more than $17 per 1,000 gallons of
treated water,  if the/influent  required extensive
pretreatment.

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                                          Section 2
                                        Introduction
This section provides background information about
the SITE Program, discusses the purpose of this
Applications Analysis Report, and describes the
Ultrox technology. A list of key contacts is provided
in Appendix A for additional information.

Purpose, History, and Goals of the Site
Program
In response  to the  Superfund Amendments and
Reauthorization Act of 1986 (SARA), EPA's Office of
Research and Development (ORD) and Office of Solid
Waste  and Emergency Response (OSWER)
established a formal program to accelerate the
development, demonstration, and use of new or
innovative technologies to clean up Superfund sites
across the country. A second program fosters the
further investigation and development of treatment
technologies  that are still at the laboratory scale.
ORD has also established a program to demonstrate
and evaluate new, innovative measurement and
monitoring technologies. These three program areas
are components of the SITE Program.

The primary purpose of the SITE Program  is to
enhance the  development and demonstration, and
thereby establish the commercial availability, of
innovative technologies applicable to Superfund
sites. Major goals of the SITE Program are to:

•  Identify and remove impediments to the
   development and commercial use of alternative
   technologies

•  Demonstrate the more promising innovative
   technologies in order to establish  reliable
   performance and cost  information  for  site
   characterization and cleanup decision making

•  Develop procedures and policies that encourage
   selection of available alternative treatment
   remedies at Superfund sites

•  Structure a development program that nurtures
   emerging technologies

EPA recognizes that a number of forces inhibit the
expanded use of  alternative technologies at
Superfund sites. One of the objectives of the program
is to identify these impediments and remove them or
design methods to promote the expanded use of
alternative technologies.

Another objective  of the SITE  Program is to
demonstrate and evaluate selected technologies. This
is a significant ongoing effort involving ORD,
OSWER, EPA Regions, and the private sector.  The
demonstration program serves to test field-ready
technologies and provide Superfund decision makers
with the information necessary to evaluate the use of
these technologies for future cleanup actions.

Another aspect of  the SITE Program includes
developing  procedures and policies that match
available technologies with wastes, media, and sites
for actual remediation.

The SITE Program also provides assistance in
nurturing the development of emerging  innovative
technologies from  the laboratory- or bench-scale to
the full-scale stage.

Technologies chosen  for a SITE demonstration must
be pilot- or full- scale applications, innovative,  and
offer some advantage over existing technologies.
Mobile technologies are of particular interest. Each
selected round of demonstrations includes at least 10
technologies.

Documentation of the Site Demonstration
Results
The results of each SITE demonstration  are
incorporated in two documents: the Technology
Evaluation Report and the Applications Analysis
Report. The Technology Evaluation Report provides a
comprehensive description of the demonstration and
its results. A likely audience for the Technology
Evaluation  Report  is engineers  responsible for
performing a detailed evaluation of the technology
for a specific site and  waste situation. These technical
evaluators seek  to understand, in detail,  the
performance of the technology during  the
demonstration and the advantages, risks, and costs of
the technology for  the  given application. This
information is used to produce conceptual designs in

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sufficient detail to enable preliminary cost estimates
for the demonstrated technology.

The Applications Analysis Report is intended for
decision makers responsible for implementing
specific remedial actions. The basic  use of the
Applications Analysis  Report is to assist  in
determining whether the specific technology should
be considered further as an option for a particular
cleanup situation. The  report discusses  the
advantages, disadvantages, and  limitations of the
technology. Costs of the technology for different
applications are estimated based on available data
for pilot-  and full-scale applications.  The report
discusses the  factors, such  as site  and waste
characteristics, that have a major impact on cost and
performance. If the candidate technology appears to
meet the needs of the site engineers, a more thorough
analysis will be conducted, based on the Technology
Evaluation Report and the Applications Analysis
Report and information from remedial investigations
for the specific site.

Purpose of the Applications Analysis
Report
To encourage  the general use  of demonstrated
technologies, EPA will provide information on the
applicability of each technology to certain sites and
wastes, other than those already tested, and will
study the costs of these  applications. Available
information and data are presented through the
Applications Analysis Reports. These reports
attempt to synthesize available information on the
technology and draw reasonable conclusions as to its
broad range applicability. The Applications Analysis
Report is very useful to those considering the
technology for Superfund cleanups and  represents a
critical   step   in   the  development   and
commercialization of the treatment technology.

Each SITE demonstration  will evaluate the
performance of a technology in treating a particular
waste found at the demonstration site. To obtain data
with broad applications, attempts will be made to
select waste frequently found at other Superfund
sites. In many cases, however, the waste at other sites
will differ in some way from the  waste tested. Thus,
the successful demonstration of a technology at one
site does not ensure that it will work equally well at
other sites. Data obtained from  the demonstration
may have to be extrapolated to  estimate the total
operating range over which the technology performs
satisfactorily. This extrapolation should be based
upon both demonstration data and other information
 available about the technology.

The amount of available data for the evaluation of an
 innovative technology varies widely. Data may be
 limited to laboratory tests on synthetic wastes, or
 may include performance data  on actual wastes
treated at pilot- or full-scale treatment systems. In
addition, there are limits to conclusions  regarding
Superfund applications that can be drawn from a
single field demonstration. A successful field
demonstration does not necessarily ensure that a
technology will be widely applicable or fully
developed to a commercial scale.


Technology Description

The Ultrox UV radiation/oxidation technology is
suitable for destroying dissolved  organic
contaminants, including chlorinated hydrocarbons
and aromatic compounds, in water  with  low
suspended solids levels. This technology uses UV
radiation, ozone, and hydrogen peroxide  to oxidize
organics. The Ultrox treatment system can be skid-
mounted for easy transport on either a flatbed truck
or in an enclosed trailer. The treatment system can
be used either as a stand-alone unit or in combination
with other treatment units.


Principal Treatment Operations
The major components of the Ultrox system are the
UV radiation/oxidation reactor module, the air
compressor/ozone generator module, the hydrogen
peroxide feed system, and the ozone decomposer
(Decompozon) unit. An isometric view of the Ultrox
system is shown in Figure 2-1.

The UV radiation/oxidation reactor used in the
demonstration (Model PM-150) has a volume of 150
gallons and is 3 feet long by 1.5 feet wide by 5.5 feet
high. The reactor is divided by  five vertical baffles
into six chambers to create a serpentine flow through
the unit. The reactor contains 24 UV lamps (65 watts
each) in quartz sheaths. The UV lamps are installed
vertically and are evenly distributed throughout the
reactor (four lamps per chamber). Each chamber also
has one stainless steel sparger that extends along the
width of the reactor.  These spargers  uniformly
diffuse ozone gas from the base of the reactor into the
water. Hydrogen peroxide is introduced in the
influent to the reactor from a storage tank. An in-line
static mixer is used to disperse the hydrogen peroxide
into the contaminated water in the influent feed line.
Acids can be added to the influent in a fashion
similar to that of the hydrogen peroxide feed.

During the Ultrox system operation, contaminated
water first comes in contact with hydrogen peroxide
as it flows through the influent line to the reactor.
The water then comes  in contact with the UV
radiation and ozone as it flows through the reactor at
a specified rate  chosen  to achieve the desired
hydraulic retention time.  The hydroxyl radicals
(OH°) are formed  from ozone and catalyzed by UV
radiation and hydrogen peroxide. The hydroxyl
radicals, in general, are known to react with organics
more rapidly than ozone, hydrogen peroxide, and UV

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                                                 Treated Off Gas
                                                                     Reactor Off Gas
                                  Catalytic Ozone Decomposer
                                                                                       Treated
                                                                                       Effluent
                                                                                       to Storage
     Water Chiller
                                                                          Ultrox
                                                                     UV/Oxidation Reactor
   Makeup
   Water
                            Dryer

                        •Compressed Air
                                      Ozone
                                    Generator
Groundwater
from Wastewater
Feed Tank
Hydrogen Peroxide
from Feed Tank
              Air
              Compressor
 Figure 2-1.  Isometric view of the Ultrox System.
radiation. The hydroxyl radicals are also much less
selective in oxidation reactions than the three other
oxidants.

Ozone that does not  go into solution with the
contaminated water will be present in the reactor off-
gas. This ozone  is subsequently destroyed by the
Decompozon unit (which contains  proprietary
catalysts and is operated at about 140°F) before being
vented to the atmosphere. The  treated water flows
from the reactor for appropriate discharge.

The flow rates at which the Ultrox system can be
operated depend on the influent waste characteristics
and the hydraulic retention time required to achieve
the  target effluent concentrations. At the
demonstration site with all 24  lamps operating,  a
hydraulic retention time of 40 minutes, an ozone dose
of 110 mg/L, and a hydrogen peroxide dose of 13 mg/L
were determined to be adequate for the treatment of
contaminated groundwater.  Since a  150-gallon
reactor was used during the demonstration, 3.75
  gallons of groundwater were treated per minute (flow
  rate). However, if higher flow rates are desired, the
  volume of the reactor  will have  to be  increased
  proportionally. For example,  assuming that the
  groundwater characteristics  and operating
  conditions  are  the same as  those  used  in the
  demonstration, a flow rate of 130 gallons per minute
  could be achieved using a larger Ultrox reactor (5,200
  gallons). The actual treatment  capacity at another
  site will likely be different, however, depending on
  the waste  characteristics and the operating
  conditions.


  Innovative Features of  the Technology
  The use of oxidants such as ozone, hydrogen peroxide,
  and UV  radiation to destroy organic contaminants
  present  in  groundwater is gaining considerable
  attention. However,  the oxidation of organics by
  ozone, hydrogen peroxide, or UV radiation alone is
  known to have kinetic limitations and, therefore, has
  yet to become a competitive treatment option.

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Several studies indicated that the kinetic limitations
could be overcome by  using  two oxidants
simultaneously (Glaze and others, 1980;  Glaze, 1987;
Weir and others, 1987; Aieta and others,  1988; and
Glaze and Kang, 1988). However, these studies did
not address the  relative performance of various
oxidant  combinations or the simultaneous use of
three oxidants.

The chemistry of the oxidation processes in which
two or three oxidants are used simultaneously is not
well  understood. However, according to Ultrox
International,  the simultaneous use of  these three
oxidants  has  a  definite  advantage  over the
simultaneous use of two oxidants  on  waters
containing compounds such as methylene chloride. In
general, processes  in  which ozone  is used  in
combination with hydrogen peroxide or UV radiation
may be categorized as catalytic ozonation processes.
These processes accelerate ozone  decomposition,
thereby increasing the hydroxyl radical  (OH°)
concentration and promoting the oxidation rate of
organics.

Oxidation  treatment of volatile  organics has
advantages over conventional wastewater treatment
methods, such as air stripping, steam stripping,
carbon  adsorption,  and biological  treatment
processes. Although effective, these processes have
certain  limitations. For example,  stripping and
adsorption merely transfer the  contaminants from
one  medium (water)  to another (air or  carbon),
whereas biological treatment  processes generate
sludge which  requires further treatment and
disposal. In addition, biological  treatment processes
have slow reaction rates. Table 2-1 compares several
treatment options for VOC-contaminated waters.
Similar  comparisons can be made for semivolatiles,
PCB, and pesticides, although  air stripping is not
generally applicable to these types of contaminants.
Table 2-1. Comparison of Technologies for Treating VOCs in Water

              Technology                 	Advantages
                	Disadvantages	
                 Inefficient at low concentrations; VOCs
                 discharged to air
                 VOCs discharged to air; high energy
                 consumption
                 Inefficient at low concentrations; requires
                 disposal or regeneration of spent carbon
                 Inefficient at low concentrations; high energy
                 consumption

                 Inefficient at low concentrations; requires
                 spent carbon disposal or regeneration;
                 relatively expensive
                 Inefficient at high concentrations; slow rates
                 of removal; sludge treatment and disposal
                 required
                 High energy consumption; process
                 mechanisms not well understood
 Air stripping

 Steam stripping

 Air stripping with carbon adsorption of vapors

 Air stripping with carbon adsorption of vapors
 and spent carbon regeneration

 Carbon adsorption


 Biological treatment
Effective at high concentrations; mechanically
simple; relatively inexpensive
Effective at all concentrations

Effective at high concentrations

Air Effective at high concentrations; no
carbon disposal costs; can reclaim the
product
Low air emissions; effective at high
concentrations

Low air emissions relatively inexpensive
 UWozorte/hydrogen peroxide oxidation (Ultrox  No air emissions; effective at all
 International)                          concentrations; VOCs destroyed; readily
                                     available
 Note: Based on Garland II, 1989.

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                                          Section 3
                           Technology Applications Analysis
Introduction
This section addresses the applicability of the Ultrox
UV radiation/oxidation technology to treat hazardous
wastes. Its applicability is based on the Ultrox SITE
demonstration and other Ultrox applications test
data. Since the results  of the SITE demonstration
provided an extensive data base,  evaluation of the
technology's effectiveness and its applicability to
other potential cleanup operations is mainly based on
these results, which are presented in detail in the
Technology Evaluation Report (EPA, 1989). The
developer's claims regarding the  applicability and
performance of the Ultrox technology are included in
Appendix B.


Technology Evaluation

The objectives of the  Ultrox  technology
demonstration performed under the SITE  Program
were to:

•   Evaluate the ability of the Ultrox system to treat
    VOCs present in the groundwater at the LB&D
    site

•   Evaluate the efficiency of the Decompozon unit in
    treating ozone in the reactor off-gas

•   Develop capital and operating costs for the Ultrox
    system  that can be  used in Superfund decision-
    making processes at other sites

•   Develop information useful to EPA Region IX for
    site remediation

With these objectives  in mind, a total of 13 test runs
were performed to evaluate  the effectiveness of the
technology. A summary of the  SITE demonstration
results,  including site characteristics,  waste
characteristics, and a review of the Ultrox system's
performance, is presented in Appendix C.

The effectiveness of the Ultrox technology  is
summarized below. The technology's effectiveness
based on the SITE demonstration is presented first,
followed by a discussion of the results from other case
studies. A fuller discussion of performance,
maintenance requirements, and costs at seven case
studies is presented in Appendix D.


Effectiveness of the Ultrox Technology

The SITE demonstration was conducted at a former
drum recycling facility in San Jose, California, over a
2-week  period in February and March of 1989.
Approximately  13,000 gallons of groundwater
contaminated with several VOCs were treated by the
Ultrox system during the 13 test runs. During the
first 11 runs, 5 operating parameters were adjusted to
evaluate the system: hydraulic retention time, ozone
dose, hydrogen peroxide dose, UV radiation intensity,
and influent pH level. The last 2 runs were conducted
to  verify the reproducibility of the system's
performance at Run 9's operating conditions, which
had been found  to  be successful at treating the
contaminated groundwater.

To  complete the demonstration within  a 2-week
period, the concentrations of indicator  VOCs in the
treated and  untreated groundwater were analyzed
overnight. Only 3 of the 44 VOCs identified in the
groundwater at the  site were selected  as indicator
VOCs for  analysis to evaluate  the  performance of
each run.  These performance indicator VOCs were
trichloroethylene (TCE); 1,1- dichloroethane  (1,1-
DCA); and 1,1,1-trichloroethane  (1,1,1-TCA).  TCE
was selected because it is  a major volatile
contaminant at the  site, and the latter two VOCs
were selected because they are relatively difficult to
oxidize.

The pH  and  alkalinity of the groundwater were 7.2
and 950 mg/L as CaCOa, respectively.  These
measurements indicated  that  bicarbonate ion
(HCOs), which acts as an  oxidant scavenger, was
present at high levels. Other oxidant scavengers such
as bromide, cyanide, and sulfide were not detected.
Organic contaminants such  as semivolatiles, PCBs,
and pesticides were also not detected.

Key findings of the  SITE demonstration are
summarized as follows:

•   Under certain  operating  conditions, the
    groundwater treated by the Ultrox system met

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   the applicable NPDES standards, at the 95
   percent confidence level, for discharge  into
   Coyote Creek, a nearby waterway. The Ultrox
   system achieved removal efficiencies as high as
   90 percent for the total VOCs present in the
   groundwater. The removal efficiencies for TCE
   were greater than 99 percent. The maximum
   removal efficiencies for 1,1-DCA and 1,1,1-TCA
   under optimal operating conditions were about
   65 and 85 percent, respectively.

•  One set of operating conditions  that  met
   discharge standards was selected as the
   "preferred",  or optimal, set of operating
   conditions. These "preferred" parameters were
   selected for verification  of subsequent runs
   during the demonstration based  on achieving
   acceptable effluent at the lowest operating costs.
   These conditions included a hydraulic retention
   time of 40 minutes, ozone dose of 110 mg/L,
   hydrogen peroxide dose of 13 mg/L, all 24 UV
   lamps (65 watts each) operating, and influent pH
   at 7.2 (unadjusted).

•  Within the treatment system, the removals of
   1,1-DCA and 1,1,1-TCA appear to be due to both
   chemical oxidation and stripping.  Specifically,
   stripping accounted for 12 to 75 percent of the
   total removals for 1,1,1-TCA, and 5 to 44 percent
   of the total removals for 1,1-DCA. However,
   stripping accounted for less than 10 percent of the
   total removals for TCE  and vinyl  chloride.
   Stripping was negligible for other VOCs, such as
   1,1-dichloroethylene, 1,2- dichloroethylene,
   benzene, acetone, and 1,1,2,2-tetrachloroethane.
   VOCs present in the gas phase within the reactor
   at levels approximately 0.1 to 0.5 ppm  were
   removed to  below detection levels in the
    Decompozon unit.

•  The Decompozon unit destroyed ozone in the
   reactor off-gas to levels less than 0.1 ppm (OSHA
    standards). The ozone destruction efficiencies
    were observed to be greater than 99.99 percent.
   There were no VOCs detected in the exhaust from
    the Decompozon unit.

•   Based on the gas chromatography (GO, and GC
    and mass spectrometry (MS) analyses performed
    for  VOCs,  semivolatile  organics,  and
    PCBs/pesticides,  no new compounds  were
    detected in the effluent. In addition, very low
    TOC removal occurred. Since VOCs made up less
    than 2 percent of the TOC, complete conversion of
    VOCs to carbon dioxide and water could not be
    verified.

 •  The Ultrox system's average electrical energy
    consumption was about 11 kilowatt-hours per
    hour of operation.
Several other studies on the performance of the
Ultrox system have been carried out. The results of
these case studies at seven facilities are summarized
in Appendix D. A brief summary of the effectiveness
of Ultrox technology  at three of those facilities is
presented below.

The  Environmental Sciences Division of the Oak
Ridge National Laboratory performed a study that
focused on the removal of VOCs from groundwater at
the  Department of  Energy  Kansas  City Plant
(Garland II, 1989). A 725-gallon unit is being used to
treat the contaminated groundwater at the site. In
addition to VOCs, the  groundwater also had bacteria,
total suspended solids (TSS), iron, manganese, and
oil and grease at  levels that  would reduce the
effectiveness of the operation. Therefore, the
groundwater  was filtered prior to treatment. The
data indicated that:  the effluent from the Ultrox
system met the applicable discharge standards for
VOCs; nitrogen (as ammonia and nitrite)  was
oxidized to nitrate; about 98 percent of bacterial
removal was achieved within the Ultrox system; but,
very little oil and grease was removed by the system.
Plugging of ozone spargers and coating of UV lamps
was  observed over  a  3-month operation, due to the
precipitation of iron and manganese within  the
Ultrox system. This required shutting down  the
Ultrox unit for a short time, which indicates that an
effective pretreatment unit is also important for the
proper functioning of the Ultrox system.

Ultrox International performed a study at  the
Hewlett Packard facility in  Palo Alto, California. A
150-gallon unit was used at this facility. This study
focused on  the removal of toxic organic compounds
such as benzene, toluene, ethylbenzene, and xylene
present in groundwater at approximate levels of
4,400, 3,300, 175, and 3,100 ug/L, respectively. The
study demonstrated that the Ultrox system could
achieve removal levels of 98 to 99.9 percent and also
that the treated effluent  could meet discharge
standards. No data were reported on operation and
maintenance problems.

A 650-gallon unit was used by Ultrox International
at FEI Microwave in Sunnyvale,  California, to
remove TCE present  in the groundwater at levels as
high as 6,000 ug/L. Removals as  high as  99.99
percent were achieved at this facility.

In summary, Ultrox International's UV radiation/
oxidation technology has been demonstrated to be
effective in removing chlorinated and nonchlorinated
organics. Although the removal of certain compounds
which are difficult to oxidize occurs significantly due
to stripping, no harmful air emissions were observed.
This is because VOCs present in the reactor off-gas
were destroyed by the Decompozon  unit before the
reactor off-gas was emitted to the atmosphere.
                                                10

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Factors Influencing Performance
Several factors influence  the performance of the
Ultrox UV radiation/oxidation technology. These
factors can be grouped into three categories: (1) waste
characteristics, (2) operating parameters, and (3)
maintenance requirements. Each of these is
discussed below.

Waste Characteristics
If, under a given set of operating conditions, the
influent contaminant levels are higher than the
contaminant levels  for  which the  operating
conditions were established, the effluent levels will
also increase, which might result in noncompliance.
However, treatment efficiency can be increased by
modifying the operating conditions to accommodate
increased influent contaminant levels. These
conditions are discussed in this section under
Operating Parameters.  If the influent contaminant
levels are anticipated to fluctuate, an equalization
tank should be provided prior to treatment in order to
minimize fluctuations.  Based on the  studies
performed,  no maximum  limit on the  influent
contaminant levels can be  specified. Also,  under a
given set of operating conditions, the  removal
efficiencies will depend upon the characteristics of
the contaminants. Key contaminant characteristics
are as follows:

•   Organics with double bonds, such as  TCE,
    tetrachloroethylene (PCE), and vinyl  chloride,
    and aromatic compounds,  such as  phenol,
    toluene, benzene, and xylene, are easily removed
    because they are readily oxidized.
•   Organics without double bonds and with high
    Henry's law constants, such as 1,1-DCA and
    1,1,1-TCA, are also removed. Removal  of these
    compounds is primarily due to stripping because
    they are difficult to  oxidize.  (Henry's law
    constants for 1,1-DCA and 1,1,1-TCA are 0.0043
    atm-m3/mol,   and   0.014  atm-m3/mol,
    respectively.)
•   Organics without double bonds and with low
    Henry's law constants, such as diethylamine and
    1,4-dioxane, would be difficult to remove because
    they are not easily oxidized or stripped.  (Henry's
    law constants for diethylamine  and 1,4-dioxane
    are 0.00009 atm-m3/mol  and 0.00001  atm-
    m3/mol, respectively.)

Since the Ultrox technology is an oxidation process
and is  intended for  the  destruction  of  organic
contaminants, any other species that consume
oxidants are considered an additional  load for the
system. These species are called scavengers and
include anions such as bicarbonates, carbonates,
sulfides, nitrites,  bromides, and cyanides. Also,
metals  present in their reduced states,  such as
trivalent chromium, ferrous iron, manganous ion,
and several others, are likely to be oxidized. These
reduced metals, in addition to acting as scavengers,
cause additional concerns. For example, trivalent
chromium, when oxidized,  will be converted to
hexavalent chromium, which is more toxic. Ferrous
iron and manganous ion are converted to less soluble
forms, which precipitate in the reactor and can cause
UV lamp scaling and suspended solids formation.
Organics (TOC) which are likely to be oxidized could
act as potential scavengers in this treatment
technology. Other parameters such as TSS, oil, and
grease reduce UV transmission and thereby decrease
the treatment efficiency.
Operating Parameters
Operating parameters are those parameters which
are varied during the treatment process to achieve
desired treatment efficiencies. Such parameters
include hydraulic  retention time, ozone  dose,
hydrogen peroxide dose, UV lamp intensity, influent
pH level, and gas-to-liquid flow rate ratio.

In general, increasing the hydraulic retention time
will increase treatment  efficiency up to a certain
point. At this point, the system tends to proceed
toward equilibrium and increasing the hydraulic
retention time no longer plays an important role.

The higher the oxidants' doses (ozone and hydrogen
peroxide), the better the treatment rate. However,
systems which use ozone and hydrogen peroxide
together are affected by the molar ratio of the
oxidants' doses used. For example,  the  expected
stoichiometry for hydroxyl radical (highly reactive
oxidant) formation from ozone and hydrogen peroxide
is two, as shown by the following equation:
       H2O2 + 2O3 ±> 2OH° + 3O2
In the treatment of water containing TCE and PCE,
researchers observed maximum removals at a molar
ratio of 2 or a 2.86 weight ratio of ozone to hydrogen
peroxide, which  agrees  with  the expected
stoichiometry (the removals were significantly less
when the molar ratio was not 2). Although, in this
case the expected stoichiometry for pure water agreed
with the molar ratio at which optimum removal was
observed, several factors may influence the molar
ratio (Aieta and  others, 1988). These factors  are
summarized below:

•   Hydrogen peroxide  can act as a  free radical
    scavenger itself, thereby decreasing the hydroxyl
    radical concentration if it is present in excess.

•   Ozone can react directly with hydroxyl radicals,
    consuming both ozone and hydroxyl radicals.
                                                11

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•   Ozone and hydroxyl radicals may be consumed by
    other constituents, known as scavengers, in the
    water being treated (see Waste Characteristics).

The optimum proportion of the oxidants  for
maximum  removals cannot  be predetermined.
Instead, the proportion needs to be determined for the
waste  under consideration using pilot-scale or
treatability tests.

UV photolysis of ozone in water yields hydrogen
peroxide, which in turn reacts with ozone to form
hydroxyl radicals. In addition, UV radiation
photolyzes compounds such as PCE,  aromatic
halides, and  pesticides to increase their removal
(Glaze and others, 1987).

The pH of water to be treated has a significant effect
on the treatment efficiency. If water has significant
bicarbonate and carbonate alkalinity (>400 mg/L as
CaCOs), lowering the pH to a range of 4 to 6 should,
in general, improve the treatment efficiency.  This is
because carbonate  and bicarbonate  ions  act as
scavengers for the oxidants. The concentration of
these  scavengers is decreased by shifting  the
equilibrium toward carbonic acid at low pH values. If
the carbonate and bicarbonate alkalinity is low, then
a high pH,  in general, should improve the treatment
efficiency.  This is  because, at a  high pH, hydroxyl
radical formation is increased due to the reaction
between ozone and the hydroxyl ion.

 The ozone gas  flow rate can  also significantly
influence the treatment efficiency. In practice, once
the ozone dose is selected, it can be applied at  several
combinations of ozone gas phase concentration and
ozone gas flow rate. According to  Venosa and
Opatken (1979), the ratio of gas flow rate to liquid
flow rate will dictate the hydraulic characteristics of
the reactor, as shown in Figure 3-1. This figure shows
that, at low gas-to-liquid flow rate ratios, the  mixing
regime in  a reactor is close to that of a plug flow
reactor (shown as Curve A), whereas at high ratios,
the reactor mixing regime is close to that of a mixed
reactor (shown as Curve C). It is advantageous to
operate the reactor with plug  flow mixing
characteristics  rather than  with mixed  reactor
mixing characteristics because a higher  treatment
efficiency is achieved for  reactions with  a positive
reaction order  (Levenspiel, 1972).  Since most
reactions have a positive reaction order, low gas-to-
liquid flow rate ratios should be considered in actual
operation of the unit. In addition to increasing the
treatment  efficiency, stripping of volatile organics
can be reduced by choosing low gas-to-liquid flow rate
ratios.
 Ma/nfenance Requirements
 The maintenance requirements for the Ultrox system
 summarized here are based on a literature review
    60
    50
   J40
  030
  s.
  Q
  9
    20
  cc
oGas Flow = 0 LVmin
a Gas Flow = 20 L/min
A Gas Flow = 80 L/min
Liquid Flow = 75 L/min
A - Plug Flow Reactor
B - Combination Flow Reactor
C - Mixed Flow Reactor
    10
                  468
                    Time, Minutes
     Source: Venosa and Opatken, 1979.
                                     10
                                            12
Figure 3-1.   Dye tests showing effects of gas flow rates on
           the mixing characteristics of a bubble diffuser
           ozone contact basin.
(Cheremisinoff and others, 1981; WPCF, 1986;
Tucker, 1986; Robson, 1987). Regular maintenance
by trained personnel is essential for the successful
operation of the Ultrox system.  The following
components require maintenance:  (1) ozonation
system, (2) UV lamp assembly, (3) ozone decomposer
unit, and (4) miscellaneous components. A brief
summary of the maintenance requirements for each
of these components is presented below.


Ozonation System
The main components of the ozonation system are the
air preparation system, the ozone generator, and the
ozone contacting and associated equipment.

The  air preparation system consists  of process
equipment  that  includes  an air filter, an  air
compressor, an optional water chiller, and a desiccant
drier. Replacement  cycles for the air filter are site-
specific, depending on air purity and flow. However,
inspection intervals for the filter should not exceed 3
months. Air compressors  should be checked as
recommended by the manufacturer to minimize  any
feed  air contamination  by  the  compressor
components.

A water chiller can be used to recirculate cooling
water  required for  the ozone generator. Tap water
(potable, suitable process water, or groundwater) can
also be used'.as a cooling water  source. If a water
chiller is used, inspections of refrigerant dryers
should be carried out at 3-month maximum intervals
by personnel  skilled  in the  operation  and
                                                 12

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maintenance of refrigeration equipment. Minimum
checks should  include compressor belt tension and
refrigerant pressure measurement. The water lines
require annual inspection for scaling or deterioration
resulting from the passage of the cooling water
through the heat exchanger.

Desiccant dryers should be inspected  weekly  to
ensure proper operation of the unit. Maintenance of
the dryers is important to keep the unit in operation
and to prevent damage to the unit by fires, which can
occur if a desiccant tower runs for a prolonged period
in the regeneration mode. Ultrox uses heatless
adsorption dryers in most air systems. These heatless
adsorption dryers are reliable and do not cause fires.
Annual maintenance should include disassembly of
the unit and inspection of the desiccant.  The media
normally lasts approximately 10 years, but may have
to be replaced sooner if the dryer has been overloaded
or poorly maintained.

The ozone generator is typically an unfamiliar unit to
maintenance personnel and may justify, at least
initially, having a maintenance  contract with the
generator supplier for emergency assistance and
annual service. Specific personnel should be assigned
to generator maintenance to enable them  to gain
sufficient familiarity and skills to perform tasks such
as fuse replacement  and dielectric tube cleaning,
which will result in lower energy costs for  a  given
ozone output. Dielectric tube cleaning necessitates
manpower and inevitable breakage or damage to the
tubes during the cleaning process. Therefore, it is
necessary to carefully evaluate the frequency  of
cleaning. It is  recommended that the first cleaning
period of the dielectric tubes not exceed  12  months
after unit start-up. Depending on the condition of the
tubes at that time, the next period of cleaning can be
projected.

Inspection of the ozone contacting equipment should
address the functional as well as the structural
integrity of the components of the contactor. Pipings,
valves, fittings, supports, brackets, and spargers
should be checked at least once  every 3 months for
the deterioration which results from exposure to a
highly oxidizing environment. Deteriorated material
should be replaced.  Good records,  including
photographs, of the conditions observed during the
inspection should be  maintained. The gas spargers
should be checked  for plugging due to solids
accumulation once  changes in the  gas  bubble
diffusion pattern are noted. The  spargers must be
immediately cleaned  to minimize cracking of joints
and excessive power costs.

The instrumentation and controls of the ozonation
system must be maintained regularly. Flow  meters,
temperature and  pressure sensors,  and ozone
analyzers must be  kept in working order to enable
the operator to measure various parameters required
for efficient operation.
UV Lamp Assembly
The maintenance of the UV lamp assembly requires
periodic cleaning and eventual replacement of the
lamps. The frequency at which the lamps should be
cleaned depends on the type and concentration of
suspended solids present in the influent or formed
during treatment. The frequency may range from
once every month to once every 3  months.  Several
cleaning procedures include the use of chemicals,
mechanical wipers, or ultrasonics.

The life of low-pressure UV lamps normally cited by
most manufacturers is 7,500' hours, based on a use
cycle of 8 hours. A number of factors combine to
effectively age the lamps, which limits their useful
life and requires their replacement. These factors
include failure of the electrodes, plating of the
mercury to the interior lamp walls (blackening), and
solarization of the lamp enclosure material (reducing
its transmissibility).  These all cause  steady
deterioration in the lamp's output at the effective
wavelength (253.7 um), such that its output at the
end of the lamp's life can be only 40 to 60 percent of
its normal output. This reduction in the output may
require more frequent replacement of the UV lamps

Ozone  Decomposer (Decompozon) Unit

The Decompozon unit, including enclosure catalyst
and heating elements, should be  inspected
thoroughly to ensure efficient  operation. Replacing
the catalyst is a considerable expenditure that can be
deferred by following  the manufacturer's
maintenance program.

Miscellaneous Components

Other components of the system, such as valves, flow
meters, pipelines, hydrogen peroxide feed tank, and
acid feed tank should be  checked for  leaks once a
month. In addition, the influent, hydrogen peroxide,
and acid feed pumps should be checked once a month
for proper operation and maintenance.

Site Characteristics
Site characteristics, in addition  to influent
characteristics and effluent discharge requirements,
are important issues  when considering using the
Ultrox  technology. Site-specific factors have both
positive and negative impacts on the implementation
of the Ultrox technology and should be considered
before  selecting this technology. These  factors
include site preparation, site access, hydrogeology,
climate, utilities, and services and supplies.
                                                13

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Site Preparation
Ultrox systems are available in several volumetric
sizes ranging in capacity from 60 to 5,200 gallons.
During the SITE demonstration, a 150-gallon unit
was used. A 20- by 20-foot area was adequate for the
Ultrox system and associated equipment. Larger
units would require slightly  larger areas. For
example, for the 5,200-gallon unit, an area about 30
by 50 feet should be provided. Areas required for
influent and effluent storage tanks, if needed, may
vary depending  on  the flow rate,  effluent
requirements, and turn-around time for any effluent
analysis required prior to its disposal.


The area containing the Ultrox unit and tanks should
be relatively level. It can be paved or covered with
compacted soil or gravel. A tent or some type of
shelter is needed for the Ultrox system to protect it
from inclement weather.

A 20- by 20-foot area is required for indoor office
space and any on- site laboratory work.
Site Access
Site access  requirements for the equipment are
minimal. The site must be accessible to tractor trailer
trucks of standard size and weight. The roadbed must
be able to support such a vehicle delivering the
Ultrox unit and tanks.
Hydrogeoiogy
At sites that require remediation of contaminated
groundwater, extraction wells will be needed to
collect the contaminated groundwater. Since the
Ultrox system would be operated as a flow-through
system  on  a continuous  basis during site
remediation,  installation of several extraction wells
may be required to provide a continuous supply of
groundwater. When installing a groundwater
collection and storage system, preventative measures
should be considered that would  reduce volatile
contaminant losses.
 Climate
 Below-freezing temperatures and heavy precipitation
 could have an impact on the operation of the Ultrox
 system. If below-freezing temperatures are expected
 for a long period of time, the Ultrox system and
 influent storage tanks should be insulated or kept in
 a well-heated shelter, such as a building or shed. The
 Ultrox unit, and particularly  the ozone generator
 which requires a high-voltage power supply, should
 also be protected from heavy precipitation.
Utilities
The Ultrox system requires tap water and electricity.
Tap water is required for equipment cleanup and
personnel decontamination. In some cases, the Ultrox
system uses tap water as a source of cooling water for
its ozone generator.

A 480-volt, 3-phase electrical service is required for
the efficient operation of the  Ultrox system. An
additional 110-volt power line will also be required
for other on-site uses.

A telephone connection  is required  to  contact
emergency  services and to provide  normal
communications.
Services and Supplies
A number of services and supplies are required for
the Ultrox technology.  Most of these services and
supplies can be readily obtained.

Tanks will likely be required for influent and effluent
storage. Extensive piping connections will be
required to assemble the groundwater collection
system.

In case any pumps or UV lamps malfunction, or any
flow meters, gas spargers, or lines crack, an adequate
on-site supply of spare parts or access to a nearby
industrial  supply  center  is an important
consideration.

Chemicals such as hydrogen peroxide and sulfuric
acid are used in this process. An adequate supply or
proximity to a supply center carrying these chemicals
is essential.

Since the Ultrox technology is designed to  treat
organics, including volatiles,  semivolatiles, and
PCBs/pesticides, entering into a contract with a local
analytical laboratory  would be prudent for an
ongoing monitoring program.

Materials Handling  Required by the
Technology
Materials handling for the Ultrox Technology can be
divided into the  pretreatment processing of the
influent before it enters the reactor unit and the
residuals handling of the air and liquid waste
streams as well as miscellaneous wastes generated
during the operation.


Pretreatment Processing

In general, the pretreatment requirements for this
technology are minimal. Depending on the waste
characteristics, pretreatment processing involves one
or more of the following: oil and grease  removal,
                                                14

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suspended solids removal, or pH adjustment to reduce
carbonate and bicarbonate levels.

Wastes containing emulsified oil and grease require
pretreatment to break down and remove emulsions. If
not treated, the emulsified oil and grease will coat the
UV lamps and reduce the UV transmission in the
Ultrox system, thereby making the process less
effective.

Pretreatment of wastes containing suspended solids
at levels greater than 30 mg/L may need to  be
considered, as the suspended solids would also reduce
the UV transmission. In addition, pretreatment may
be necessary for wastes containing dissolved metals,
such as iron and manganese, which have  lower
solubilities at higher oxidation states. The removal of
such metals is required because they will be oxidized
and precipitated  in the Ultrox system, resulting in
the formation of suspended solids and, also, scaling of
the UV lamps.

pH adjustments may need to be considered for wastes
having bicarbonate and carbonate  ions at levels
greater than 400 mg/L as CaCOa. These ions act as
oxidant scavengers and cause  additional load to the
treatment system. If required, pH adjustments can be
performed in-line.

Even if no pretreatment is  needed, the aqueous
organic wastes may still need to be pumped to  an
equalization tank (such as bladder tanks to minimize
VOC losses) to reduce flow and concentration
fluctuations. If so, plumbing connections will  be
needed.
Residuals Handling
Two major types of residuals are generated from the
Ultrox treatment system: (1) air emissions and (2)
treated effluent. The Ultrox system did not generate
any harmful air emissions during the demonstration.
The ozone decomposer unit in  the Ultrox system
removed the ozone and VOCs present in the reactor
off-gas to environmentally safe levels. Therefore, no
special residual handling procedures were required
for the air emissions at the  demonstration  site.
However,  periodic monitoring of air emissions for
ozone and VOCs is recommended.

Air emissions are treated by the Decompozon unit
(Model 3014  FF), which uses a nickel-based
proprietary catalyst and operates at about 140°F to
decompose reactor off-gas ozone to  oxygen. The
Decompozon unit can accommodate flows of up  to 10
standard cubic feet per minute and can destroy ozone
concentrations  in ranges of 1 to 20,000 ppm (by
weight) to less than 0.1 ppm.

The treated water could be disposed of either on- or
off-site. Examples of on-site disposal options for the
effluent include groundwater  recharge and
temporary storage on-site for sanitary usage.
Examples of off-site disposal options are discharge
into rivers, creeks, storm sewers, and sanitary
sewers. Bioassay tests may be required in addition to
routine chemical and physical analyses before the
effluent is disposed of. During the demonstration, the
treated water was stored in a 20,000-gallon  metal
tank until laboratory  analyses  indicated that the
water met  NPDES  standards.  Subsequently, the
effluent was discharged into Coyote  Creek, a nearby
waterway.

In addition to these principal residuals, the operation
of the Ultrox system also requires the handling and
replacement of miscellaneous items related to the
operation. These items include UV lamps, spargers,
and filters which may be  required to treat the
influent. To avoid excessive analytical costs to
determine whether  or  not  these items are
nonhazardous, disposal of these  items as hazardous
wastes seems warranted.

Personnel Requirements
Personnel trained to operate the Ultrox system are
needed to ensure a reliable operation.  Operating
personnel requirements depend on the size of the
Ultrox system purchased, as well  as the features
included on the unit. For example, the Ultrox system
(Model F-4000), which has been in operation at the
Sealed Power Corporation in Muskegon, Michigan, is
totally automated and, therefore, requires minimal
attention. This system has alarms to indicate power
failure,  high ambient ozone levels, and any
malfunctioning of the  system components, such as
the Decompozon unit and the air compressor. These
alarms can be connected to the control/security room,
where the facility operator or security personnel is
stationed. At the sound of an  alarm,  all system
components and the wastewater flow will be shut off,
and the problem area will be indicated on the control
unit for proper  action. Typically with this type of
unit, a 15-minute routine inspection  at the beginning
and end  of each  day  by an operator  with  basic
mechanical skills is adequate. Typically, no operator
attention is needed in the evenings or on weekends.

A person capable of collecting samples from taps and
performing wet chemistry analysis  (measuring pH,
oxidant concentrations, etc.) is required to monitor
the Ultrox system operation  once a day. These
analyses may  take about an hour. Samples for
organic analyses can be sent to a contract laboratory.

A project supervisor is required to  provide general
technical guidance. This person should have an
understanding  of the treatment process and be
capable of reviewing data to evaluate the system's
performance. About 2 hours per week of the project
supervisor's time should be adequate.
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The operating personnel are subject to OSHA
regulations. According to OSHA, the  maximum
allowable ozone exposure for an 8-hour period is 0.1
ppm. When functioning properly, the Decompozon
unit reduces ozone levels in the reactor off-gas to
about 0.001 ppm and,  therefore, alleviates  this
concern. However, other health and safety issues due
to the contaminants present in the untreated aqueous
waste will be site-specific. Therefore, a site-specific
Health and Safety Plan should be prepared. This plan
should include the facility description, a list of
chemicals of concern and their concentrations, health
and safety zones, personnel protective clothing and
equipment, contaminant monitoring procedures,
hospital routes, and the personnel to contact in the
event of an emergency.

Potential Community Exposures
Contaminant emissions from the Ultrox system are
minimal. The Ultrox system, equipped  with its
Decompozon air treatment system, destroys ozone
present in the reactor off-gas to nondetectable levels.
The SITE demonstration  data indicated  that the
Decompozon unit also reduced the VOC levels
present in the reactor off-gas to nondetectable levels
when the Decompozon unit functioned properly.
Therefore, no major potential for on- site personnel or
community exposure  to air-borne contaminants is
anticipated.  In case of any malfunctioning, all
components of the system and unit will shut off
automatically, leaving no threat to the community.

Regulatory Requirements
This  subsection discusses  the regulatory
requirements for the  Ultrox system as they relate to
conducting a hazardous waste site remediation.

Comprehensive Environmental Response,
Compensation, and  Liability Act
The Comprehensive Environmental Response,
Compensation, and Liability Act (CERCLA) of 1980,
authorizes the Federal government to respond to
releases or potential  releases of any hazardous
substance into the environment, as well as to releases
of pollutants or contaminants that may present an
 imminent or significant danger to public health and
 welfare or the environment.

 The Superfund Amendments and Reauthorization
 Act of 1986 (SARA) amended CERCLA,  and directed
 EPA to:

 •   Use remedial alternatives that permanently and
     significantly reduce the volume,  toxicity, or
     mobility of hazardous substances, pollutants, or
     contaminants
•  Select remedial actions that protect human
   health and the environment, are cost-effective,
   and involve permanent solutions and alternative
   treatment or resource recovery technologies to
   the maximum extent practicable
•  Avoid off-site transport and disposal of untreated
   hazardous substances or contaminated materials
   when practicable treatment  technologies exist
   (Section 121 (b))

As part of the requirements of CERCLA, EPA has
prepared the National Contingency Plan (NCP) to
address responses  to releases  of hazardous
substances. The NCP (codified in 40 CFR Part 300)
delineates the methods and  criteria used to
determine the appropriate extent of removal and
cleanup for hazardous waste contamination. The
NCP includes chemical oxidation as a direct waste
treatment method that can be considered a long-
term, permanent solution for  remediating
contaminated groundwater at CERCLA sites (Part
300.70(B)(5)).

In general, there are two types of responses possible
under CERCLA: removal and  remedial actions.
Chemical oxidation technologies can be part of a
CERCLA removal action. However, if the removal
action is part of a remedial action, the removal action
will be limited in the amount of time and  money
spent to implement the response. Superfund-financed
removal actions cannot exceed 12 months in duration
or $2 million in cost in most cases (Section 104(c) (1)).

Remedial actions are  governed by   SARA
amendments  to CERCLA. As stated above, these
amendments promote remedies  that permanently
reduce the volume, toxicity,  and  mobility  of
hazardous substances, pollutants, or contaminants.
Section 121(c),  of CERCLA as amended by  SARA,
requires EPA to review any remedial action in which
hazardous substances, pollutants, or contaminants
remain at the site.

Because each hazardous waste site is unique and has
 specific contamination characteristics, a discussion of
 all potential applicable or relevant and appropriate
 requirements (ARAR) for a given remedial action
 involving chemical oxidation cannot be covered in
 this regulatory  analysis. On-site remedial  actions
 must comply with Federal and more stringent state
 ARARs that are determined on a site-by-site basis.
 ARARs will dictate the degree of cleanup necessary
 at CERCLA sites, and CERCLA provides only six
 waivers to meeting ARARs during a remedial action
 (Section 121(d)(4)). If chemical oxidation is chosen as
 the sole technology for a remedial action, then the
 chemical oxidation  process must meet ARARs for
 cleanup at the site.
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Section 121(e)(l) specifies that no Federal, state, or
local permit is required for the portion of any removal
or remedial action conducted entirely on-site.
However, the remediation must comply with all
substantive regulatory requirements.


Resource Conservation and Recovery Act

RCRA, an amendment to the  Solid Waste Disposal
Act, was passed in 1976 to address the problem of how
to safely manage and dispose of municipal and
industrial solid wastes. RCRA specifically addresses
the identification and  management of hazardous
wastes. The  Hazardous  and  Solid  Waste
Amendments of 1984 (HSWA) significantly expanded
the scope and requirements  of RCRA,  including
prohibiting the land disposal  of hazardous wastes
that do not meet promulgated treatment standards.

RCRA regulations  concerning hazardous waste
identification and management are specified  in 40
CFR Parts 124, 260-272. EPA and RCRA- authorized
states implement and enforce RCRA  and  state
regulations.

The key to determining whether RCRA regulations
apply to  the Ultrox  process is  whether the
contaminated media is a  hazardous waste. EPA
defines hazardous waste in 40 CFR Part 261. If
hazardous wastes are treated by chemical oxidation,
the owner/operator  of the  treatment or disposal
facility must obtain a RCRA permit from EPA or
RCRA-authorized state. RCRA requirements for
permits are  specified  in 40 CFR Part  260.
Requirements for hazardous waste generators are
specified in 40 CFR Part 262, and include obtaining
an EPA identification number prior to treating
hazardous wastes. The requirements for a  hazardous
waste generator  will be applicable if contaminated
groundwater is determined to be a hazardous waste,
and is extracted for treatment, storage, or disposal.

In some situations, chemical oxidation may be used
as part of a pump and treat remediation method. In
these cases, the owner or operator  of the  treatment
system will have to  comply with 40 CFR Part 265,
Subparts B (General Requirements)  and  Q
(Chemical, Physical,  and Biological Treatment).

If hazardous wastes  are generated in batches and
must be stored on-site prior  to treatment, other
RCRA regulations may apply. These regulations may
include complying with 90-day accumulation limits
for facilities without hazardous waste storage
permits (40 CFR  Section 262.34), complying with 40
CFR Part 264 or 265, Subpart I, if hazardous wastes
are stored in containers, and complying with 40 CFR
Part 264 or 265, Subpart J, if hazardous wastes are
stored in tanks. In addition,  small  quantity
generators cannot store  more than 6,000 kg of
 hazardous waste on-site without a permit (40 CFR
 Section 262.34(D)).

 Once hazardous wastes are treated by chemical
 oxidation, the treated waste must be analyzed to
 determine  if it still contains  any  hazardous
 properties or constituents. As such, subsequent
 management of the treated waste may also be subject
 to the above RCRA requirements, until  these
 analyses are performed. Other applicable RCRA
 requirements could include the use of a Uniform
 Hazardous Waste Manifest if the waste is transported
 off-site and restrictions as to where the treated waste
 can be discharged.

 Currently, air  emissions from hazardous waste
 treatment operations are not addressed by RCRA
 regulations.  However, Section 3004(n) of RCRA
 directs EPA to issue regulations concerning air
 emissions from hazardous waste treatment, storage,
 and disposal facilities.

 RCRA Corrective Action

 RCRA regulations (Sections  264.100  - 264.101)
 require that a corrective action program be instituted
 as necessary to protect human health and the
 environment from all releases of hazardous waste or
 its constituents from any solid waste management
 unit.  The corrective action program must  be in
 compliance with groundwater protection standards
 and must begin within a reasonable amount of time
 after the groundwater protection standard has been
 exceeded. The contaminated water must be treated to
 the levels determined in the corrective action order.
 These levels can vary, depending on  state and local
 requirements  (e.g., NPDES, publicly-owned
 treatment works (POTW), or maximum contaminant
 levels (MCL)).

 Additionally, a groundwater monitoring program
 must be implemented to prove  that  the corrective
 action program has been effective. Corrective action
 must be completed during the compliance period to
 the extent necessary to ensure that the groundwater
 protection standard is met. However, if corrective
 action is being performed at the end of a compliance
period, that corrective action must continue for as
 long as necessary to achieve compliance with the
 groundwater protection standard.

 Clean Air Act

The Clean Air Act requires that treatment,  storage,
and disposal facilities  comply with primary and
secondary ambient air quality standards. Since
volatile organic air emissions are possible during the
extraction or  transfer of the contaminated water to
the treatment unit,  steps need to be taken to prevent
or minimize  the potential impact  from organic
vapors. Preventative measures could include storing
                                               17

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the contaminated water in  an enclosed tank or
container.

During treatment, steps must be taken to minimize
the  release of ozone  into  the atmosphere.
Furthermore, any release of ozone must be no more
than 0.12 ppm, in accordance with 40 CFR Section
50.9 (national primary and secondary ambient air
quality standards for ozone).  Ultrox's Decompozon
unit is specifically  used to  destroy ozone in the
reactor off-gas.

State air quality standards may require additional
measures to prevent volatile  organic air emissions,
including the release of ozone.

Clean Water Act
The Clean Water Act (CWA),  as amended by the
Water Quality Act of 1987, describes standards and
enforcement for discharges, including toxic and
pretreatment effluent standards which are applied
primarily to protect surface water quality. The CWA
established the National Pollutant Discharge
Elimination System (NPDES),  which requires that
(1) EPA publish water quality criteria for pollutants
and (2) each state set water quality standards, using
the EPA criteria, for every significant body of surface
water within its borders. States then issue permits
for discharges into these bodies of surface water.

NPDES requirements are specified in 40 CFR Part
122. Part 122 requires  that contaminated water be
treated to appropriate levels prior to discharging into
a storm sewer  or surface waterbody. If  chemical
oxidation is used as part of an industrial process or as
a RCRA-corrective action and the treated water is
discharged to  a surface waterbody, a NPDES
discharge permit must be obtained.

Safe Drinking Water Act
The Safe Drinking Water Act  (SDWA) of 1974, as
most recently amended by the Safe Drinking Water
Amendments of 1986,  requires EPA  to establish
regulations to  protect human health  from
contaminants in drinking water. The legislation
authorized  national  drinking water standards and a
joint Federal- state  system for  ensuring compliance
with these standards.

The National Primary  Drinking Water Standards
are found  in 40 CFR  Part 141. Under SDWA,
maximum  contaminant  levels (MCL), which are
enforceable standards for  chemicals in  public
drinking water supply  systems, were established.
MCLs consider both health factors and the economic
and technical feasibility of removing a contaminant
from a water supply system.  Treated water injected
into groundwater used  as a  public drinking water
source must meet the MCLs.
Toxic Substances Control Act

The Toxic Substances Control Act (TSCA) of 1976, as
codified in 40  CFR Parts  700  through 799,
established requirements and authorities  for
identifying and controlling toxic chemical hazards to
human health and the environment. The disposal of
PCBs is specifically regulated under Section 6(e) of
TSCA, with PCB treatment and disposal regulations
specified in 40 CFR Section 761.60.

Soil contaminated with PCBs  may be encountered
when boring groundwater extraction and monitoring
wells. PCBs in concentrations between 50 and  500
ppm may be disposed of in either a TSCA-permitted
landfill or destroyed at a TSCA-approved incinerator
(40 CFR Section 761.70).

TSCA does not regulate treatment or disposal of
water contaminated with PCBs at concentrations  less
than 50 ppm, which is typically  found during
groundwater remedial actions.

Occupational Safety and Health Act
Superfund remedial actions and RCRA-corrective
actions must be  performed in accordance with  the
Occupational Safety and Health Act (OSHA)
requirements codified in 29 CFR Parts 1900 through
1926. During site preparation, a pad, made of
compacted gravel or concrete, will likely have to be
constructed to  place the  Ultrox  unit on.  The
construction of this pad must be performed in
accordance with Part 1926 of OSHA (Safety  and
Health Regulations for Construction).

A weather shelter to provide protection for the Ultrox
system from  inclement  weather and to provide
suitable work environment for on-site  personnel
needs to be constructed. The complexity  of this
shelter will depend on the climate where the site is
located and the duration of treatment. For the Ultrox
demonstration in San Jose, California, a large
awning proved sufficient. However, in areas without
year-round, mild climates, it may be necessary to
build a sturdy and durable enclosure.

Since the  Ultrox unit operates on electricity, utility
hookups are needed. Construction of these hookups
must be performed in accordance  with Part 1926,
Subpart K (Electrical) of OSHA. If the utility lines
are placed underground,  the excavation  performed
must follow the requirements specified in Part 1926,
Subpart P of OSHA.

Although the Ultrox system requires little personnel
involvement  once it is operating  under desired
conditions, technicians performing daily and weekly
monitoring and sampling must  wear  personnel
protective equipment, such as rubber gloves and eye
guards (Part 1910, Subpart I). Additional personnel
                                                18

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protective equipment may be needed when handling
untreated waste.
State occupational safety and health requirements
may be significantly stricter than Federal standards.
                                                19

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                                           Section 4
                                     Economic Analysis
Introduction
The costs associated with the Ultrox technology are
defined by 12 cost categories that reflect typical
cleanup activities  at Superfund and RCRA-
corrective action sites.  Each of these categories is
defined and discussed, thereby forming the basis for
the estimated cost analysis presented in Table 4-1 for
an Ultrox UV technology operation. Annual
operating and maintenance costs and one-time costs
are presented in Table  4-1 for three treatment flow
rates: 20, 100, and 250  gpm. The costs presented in
this analysis are order-of-magnitude (-30 to +50
percent) estimates, as defined by the American
Association of Cost Engineers.

Site-Specific Factors Affecting Cost

Several factors affecting the cost of the Ultrox system
are highly site-specific,  and are difficult to calculate
without the benefit of data from an accurate site-
remedial investigation report. The factors  most
affecting cost include: volume of aqueous waste to be
treated; extent of contamination; site condition (in
terms of necessary  site preparation, such as
constructing access  roads and regrading for  a
treatment  pad, etc.); treatment  goals to meet
discharge requirements; and frequency of equipment
repair and replacement.

Basis of Economic Analysis

The Ultrox  technology can be operated in a batch or
continuous mode  depending upon treatment
requirements. For  the purpose of this economic
analysis, it is assumed that the  system will be
operated in  a continuous mode, 24 hours a day, 7 days
a week, for one year.  During this  period the unit
should treat approximately 10.5 million  gallons in
the 20-gpm  unit, 52.5 million gallons in the 100-gpm
unit, and 131.5 million gallons in the 250-gpm unit.
One year was chosen as the period of time for this
Table 4-1. Estimated Costs Associated with Three Ultrox System Units
                                                                Estimated Costs (1990 $)
Item
Site Preparation Costs3
Permitting and Regulatory Costs3
Capital Equipment Costs3
Startup and Fixed Costs3
Labor Costsb
Supply and Consumable Costsb
Utility Costsb
Effluent Monitoring and Disposal Costsb
Residuals and Waste Shipping, Handling, and Transporting Costsb
Analytical Costs'3
Equipment Repair and Replacement Costs'5
Site Demobilization Costs3
20 gpm
36,000
3,500
70,000
32,000
6,600
10,500
12,000
3,000
1,000
24,000
4,000
2,000
1 00 gprn
55,000
7,500
150,000
32,000
6,600
16,500
58,000
3,000
5,000
24,000
22,000
3,000
250 gpm
75,000
13,000
260,000
32,000
6,600
20,800
145,000
3,000
7,000
24,000
33,000
4,000
        Total One-Time Costs
        Total Annual Operation and Maintenance Costs
   143,500
   61,100
247,500

135,100
384,000

239,400
3 One-time costs
b Annual operation and maintenance costs
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analysis so that reliable  annual operating and
maintenance costs could be determined. However, it
should be noted that most groundwater remedial
actions require a significant amount of time (e.g., 5 to
30 years).

In addition, it is assumed that the groundwater is
contaminated with  VOCs such as TCE and  vinyl
chloride, at levels of 100  and 40 ug/L, respectively.
The operating conditions  assumed for  this analysis
are as follows: a hydrogen peroxide dose of 16 mg/L;
an hydraulic retention time of 60 minutes; an ozone
requirement of 14 Ibs/day at 2 percent weight in air;
and all UV lamps operating at 100 percent efficiency.
The contaminants were assumed to be treated to
meet  NPDES standards for discharge  into a storm
drain or nearby waterway.

The following is a list of assumptions  used for this
analysis:

•  Utility connections will be overhead

•  Suitable access roads exist

•  Contaminated water is in a shallow aquifer

•  Installation of the Ultrox system at  the site is not
   included in the capital equipment cost

•  One technician,  one hour per day,  seven days a
   week will check and maintain the system

•  One supervisor, two  hours per week,  will
   supervise the technician

•   Labor costs associated with major repairs are not
   included

•   Spent UV lamps from the treatment process are
   considered a hazardous waste

•   One treated water sample  will be taken  each
    month and tested for organic compounds

•   UV lamps will be replaced annually

•   Site demobilization only includes  transporting
    the Ultrox unit off-site

•   Decommissioning equipment and disposal costs
    are not included.

A detailed discussion of each of the 12 cost categories
in Table 4-1 is provided below.
 Site Preparation Costs
 The costs associated with site preparation include
 planning and management, system design, auxiliary
 and temporary equipment and facilities,  legal
 searches, access rights, preparation for support
 facilities, minor cleaning of the site, emergency and
 safety equipment, utility connections, constructing
foundations, installing monitoring and extraction
wells if groundwater is the aqueous waste, startup,
and site support staff.

Site  preparation costs will vary depending on the
type of site where the treatment operation takes
place and the condition of the site. Sites that require
major cleaning and regrading for the foundation will
significantly increase site preparation  costs. Utility
connections can be either overhead or buried;
however, the latter option will require more design,
planning, and construction. For this analysis, it is
assumed that utility connections will be overhead. In
addition, some sites may require the construction of
access  roads; however, this analysis, assumes that
suitable access roads already exist.

Installing monitoring and extraction wells are a
significant portion  of site preparation costs,
depending on the depth of the  groundwater to be
monitored and extracted. The Ultrox system can also
be used to treat contaminated surface water. In such
a case, a pump system may need to  be installed,
including a filtration system to screen out debris and
any other solids. It is assumed for this analysis that
contamination is present in a shallow aquifer.  Site
preparation costs are estimated  to be approximately
the following: $36,000 for a 20-gpm unit; $55,000 for
a 100-gpm unit; and $75,000 for a 250-gpm unit.


Permitting  and Regulatory Costs
Permitting and regulatory costs will vary depending
on whether treatment is performed on a Superfund or
a RCRA-corrective action site  and on how  the
effluent is  disposed. Section 121(d) of CERCLA as
amended by SARA requires that remedial actions be
consistent  with ARARs for environmental laws,
ordinances, regulations,  and statutes.  ARARs
include Federal  standards and criteria as  well as
more stringent standards  or criteria  promulgated
under state or local jurisdictions. Applicable
requirements are those for which the  jurisdictional
prerequisites of the underlying statute are satisfied.
Relevant and appropriate requirements  do  not
legally apply to the situation or action planned, but
are  none the  less suitable because  of the
characteristics of the remedial action, the pollutants
in question, or the physical circumstances at the site.
ARARs must be determined on a site-specific basis.

At RCRA-corrective action sites, analytical protocols
and annual monitoring records will have to  be kept,
which will increase the regulatory costs. For these
situations, an additional 5 percent should be  added to
the  estimate  rendered for  this  category.
Contaminated soil removed during the  installation of
monitoring and extraction wells will have to be
stored in  compliance  with RCRA or state
requirements. Soil that will be disposed of  at a
permitted landfill will have to meet Federal or state
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land disposal restriction requirements. This may be
very difficult and costly for PCB- contaminated soil.
and fixed costs are estimated to be approximately
$32,000.
Permitting and regulatory costs are assumed to be
approximately 5 percent of the capital equipment
costs for a treatment operation that is  part of a
Superfund remedial action. This estimate does not
include annual discharge permit costs which may
vary significantly depending on state and local
requirements.


Capital Equipment Costs

Capital equipment costs include the cost of an Ultrox
reactor, an air compressor, an ozone generator, and a
hydrogen peroxide feed system. Based on information
provided  by Ultrox International, these  costs are
$70,000 for a 20-gpm unit, $150,000 for a 100-gpm
unit, and $260,000 for a 250-gpm unit. Installation
costs are not included in these estimates but are
assumed  to be approximately 5 to 7 percent of the
capital equipment costs.


Startup and Fixed Costs

Startup costs  include those required to  establish
operating procedures, train operators, perform an
initial shakedown of the equipment and  analysis,
construct a shelter to protect the system, and initiate
an environmental monitoring program.

To ensure safe, economical, and efficient operation of
the unit,  a program to train  operators is necessary.
The costs associated with  this training  program
include developing a health and safety program and
associated manuals, providing health and  safety
training,  and providing  training for operating and
maintaining the system.  At least three persons (i.e.,
two technicians and one supervisor) will need health
and  safety training, with the supervisor  receiving
health and safety supervisory training in addition.
These individuals  will be  responsible  for  daily
monitoring and will have to be instructed  by Ultrox
personnel about  operating  and maintaining the
system. Startup training costs are estimated to be
approximately $7,500. This estimate is  based on
three 40-hour health and safety training courses, one
health and safety supervisory training course, and
three weeks of instruction for the three individuals
from Ultrox's staff.

Mobilization and shakedown costs  include the
transportation of the unit to the site, initial  setup, on-
site  checkout, construction  of a weather shelter,
construction supervision, working capital, and
analysis  to  determine the proper operating
parameters for treatment. These costs  are site-
specific and will vary depending on the location of the
site. Personnel travel  costs to the site are not
included. For this analysis, equipment shakedown
and analysis are assumed to be $20,000. Total startup
Labor Costs

Once the Ultrox UV radiation/oxidation system is
assembled and shakedown has been completed, the
system requires very little labor for operation. Based
on information provided by the developer, from case
studies, and from the operation of other similar
groundwater treatment systems, it is assumed that a
skilled technician will be needed for one hour a day,
seven days  a week, to  check and maintain  the
equipment and take routine water and air  samples.
This analysis assumes that two individuals will split
this job (one during the  week and one during the
weekend) and that they  will  be  working on  other
remediation efforts the remaining seven hours in
their workshift.  In addition,  a supervisor will be
needed for two hours per week, to oversee the work
performed by the technicians.  It is assumed that the
technician  will be paid $10 per  hour and  the
supervisor will be paid $20 per hour (fringe benefits
are not included). The annual operating labor costs
will be approximately $3,600 for the technician and
$2,100 for the supervisor. The two technicians and
the supervisor will require an annual health and
safety refresher course and it  is estimated that this
will cost $900 annually. Total  annual labor costs are
assumed to be $6,600. This estimate does not include
labor costs associated with major equipment repairs.

Supply and  Consumable Costs
Supplies and consumables  for  the Ultrox UV
radiation/oxidation  system include  hydrogen
peroxide, acids for pH adjustment, and other
miscellaneous supplies. The quantities of hydrogen
peroxide and acid used depend upon the size of the
system employed  and the level  of organic
contamination in the waste stream. These costs are
assumed to be approximately 15 percent annually of
capital equipment costs for  the  20-gpm unit, 11
percent for the 100-gpm unit,  and 8  percent for the
250-gpm unit. These estimates represent the average
costs of these items incurred during implementation
of the Ultrox system at other sites. The cost of the
supplies is expected to significantly decrease with the
larger volume units, due to economies of scale.


Utility Costs
The Ultrox system runs on commercial electricity.
Utility costs reflect the amount of electricity needed
to operate the  ozone generator, the  UV
radiation/oxidation reactor with its lamps,  and site
support facilities. The quantity of electricity used
depends on the quantity of groundwater treated, the
amount of ozone needed, the level  of contamination,
and the retention time.  It is estimated that  the
electrical cost will be $1.10 per 1,000 gallons treated,
                                                23

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based on averages from other case studies and
estimates from several utility companies.


Effluent Monitoring and Disposal Costs
This cost category consists of effluent monitoring and
a supply and storage or source of clean water for
personnel and equipment decontamination. Effluent
monitoring will be performed routinely by the
technician. The effluent will  be discharged to a
nearby storm drain  or  reinjected  into the
groundwater. The cost estimate for this category is
based  on discharge to a storm drain and is
approximately $3,000 per year.


Residuals and Waste Shipping, Handling, and
Transportation  Costs
The Ultrox UV  radiation/oxidation process produces
very few residuals that require special handling.
Filters and UV lamps may need to be disposed of
following treatment due to a buildup of residuals and
corresponding reduction in effectiveness and
efficiency. Spent UV lamps are considered hazardous
because they contain mercury and will  therefore
require disposal at a permitted facility. Residuals
shipping, handling, and transporting costs to a
hazardous waste disposal facility are assumed to be
between $1,000 and $7,000 per  year for the 3 Ultrox
units, based on disposal costs of $500 per drum.


Analytical Costs
Analytical costs include laboratory analyses, data
reduction and tabulation, quality assurance/quality
control (QA/QC), and reporting. Monthly laboratory
analyses will cost approximately $1,250, while data
reduction and  tabulation,  QA/QC, and reporting
should cost $500 to $750 dollars per month. This
analysis assumes that  one organic treated
water sample, will be taken each month. Total
estimated  analytical  costs are,  therefore,
approximately $24,000 per year.


Equipment Repair and Replacement Costs
During the course of operation, certain parts of the
Ultrox system will need to be  replaced. The most
common parts needing  replacement are the UV
lamps, spargers, and influent feed line filters. The 20-
gpm unit contains 36 lamps, the  100-gpm unit has
288 lamps, and the 250-gpm unit has 432 lamps. UV
lamps will have to be replaced annually, at a cost of
$60 per lamp installed. Annual equipment repair and
replacement costs are estimated to be approximately
5.7 percent of the capital costs for the 20-gpm unit;
14.7 percent of the capital costs for the 100-gpm unit;
and 16 percent of the capital costs for the 250-gpm
unit. It is assumed for this analysis that the cost of
filters and spargers will decrease due to economies of
scale.

Site Demobilization Costs
Site demobilization will include operation shutdown,
site cleanup and restoration,  permanent storage
costs, and site security. Site demobilization costs will
vary depending on whether the treatment operation
occurs at a Superfund site or at a RCRA-corrective
action site. Demobilization at the latter type of site
will require detailed closure and post-closure plans
and permits. Demobilization at a Superfund site does
not require as  extensive post-closure care; for
example, 30-year monitoring is not required. This
analysis assumes site demobilization costs cover only
those items involved with transporting the Ultrox
units and are assumed to vary between $2,000 and
$4,000 for the  different  treatment  units.
Decommissioning equipment and disposal costs are
not included in this estimate.
                                                24

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                                        References
Aieta, E.M., K.M. Reagan, J.S. Lang, L. McReynolds,
   J.W. Kang, and W.H. Glaze, 1988.  Advanced
   Oxidation Processes for Treating  Groundwater
   Contaminated with TCE and PCE: Laboratory
   Studies, Journal of the American  Water Works
   Association, 5:64.

Cheremisinoff, N.P., P.N. Cheremisinoff, and R.B.
   Trattner, 1981. Chemical and Nonchemical
   Disinfection, Ann Arbor Science Publishers, Inc.,
   Michigan.

EPA,  1989. Technology Evaluation Report, SITE
   Program  Demonstration  of  the  Ultrox
   International Ultraviolet Radiation/Oxidation
   Technology, EPA/540/5-89/012.

Fletcher, D.B., 1987.  UV/Ozone Process Treats
   Toxics, Waterworld News, 3:25.

Garland II,  S.  B., 1989.  Annual  Report, An
   Evaluation of the Use of a Combination of Ozone,
   Ultraviolet Radiation, and Hydrogen Peroxide to
   Remove Chlorinated  Hydrocarbons  from
   Groundwater at the Department of  Energy
   Kansas  City Plant, Oak  Ridge National
   Laboratory Report, ORNL/TM-11056.

Glaze, W.H., G.R. Peyton, F.Y. Huang, J.L. Burleson,
   and P.C. Jones, 1980. Oxidation of Water Supply
   Refractory Species by Ozone with Ultraviolet
   Radiation, EPA-600/2-80-110.

Glaze, W.H., 1987. Drinking Water Treatment with
   Ozone, Environmental Science and Technology,
   21:3:224.
Glaze, W.H., J.W. Kang, and D. H. Chapin, 1987. The
   Chemistry  of Water Treatment Processes
   Involving Ozone, Hydrogen Peroxide,  and
   Ultraviolet Radiation,  Ozone Science  and
   Engineering.

Glaze, W.H., and J.W. Kang,  1988. Advanced
   Oxidation Processes for Treating Groundwater
   Contaminated with TCE and PCE: Laboratory
   Studies, Journal  of the American Water Works
   Association, 5:57.

Levenspiel,  O.,  1972.  Chemical Reaction
   Engineering, Second Edition, John Wiley & Sons,
   Inc., New York.

Robson,  C.M.,  1987. Engineering  Aspects of
   Ozonation, Waterworld News, 3:18.

Tucker,  A.L.,  1986.  Refining UV Systems,
   Waterworld News, 4:16.

Venosa,  A., and E.J. Opatken, 1979. Ozone
   Disinfection  - State of the Art. In:  Proceedings,
   Pre-conference  Workshop on  Wastewater
   Disinfection, Atlanta,  GA,  Water Pollution
   Control Federation.

Weir, B.A., D.W. Sundstrom, and H.E. Klei, 1987.
   Destruction  of Benzene  by Ultraviolet Light-
   Catalyzed Oxidation with Hydrogen Peroxide,
   Hazardous  Waste and Hazardous Materials,
   4:2:165.

WPCF, 1986. Wastewater Disinfection, Manual of
   Practice No. FD-10, Alexandria, Virginia.
                                              25

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             Appendix A
Key Contacts for the SITE Demonstration
                 27

-------
                      Appendix A Contents
                                                             Page
The Ultrox Technology  	  29
The SITE Program 	  29
The Demonstration Site  	  29
                                28

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                                        Appendix A
                     Key Contacts for the SITE Demonstration
Additional information on the Ultrox technology, the
SITE Program, and the demonstration site can be
obtained from the following sources.

The Ultrox Technology

David B. Fletcher
President
Ultrox International
2435 South Anne Street
Santa Ana, CA 92704
(714) 545-5557

The SITE Program

SITE Program,  EPA Headquarters
Jim Cummings
U.S. Environmental Protection Agency
Office of Solid Waste and Emergency Response
Office of Policy, Management, and Technology
401 M Street, S.W.
Washington, DC 20460
(202) 382-4362

SITE Project Manager, Ultrox Demonstration
Norma M. Lewis
U.S. Environmental Protection Agency
Office of Research and Development
Risk Reduction Engineering Laboratory
26 West Martin Luther King Drive
Cincinnati, OH 45268
(513) 569-7665
Chief, SITE Demonstration and Evaluation Branch
Steve James
U.S. Environmental Protection Agency
Office of Research and Development
Risk Reduction Engineering Laboratory
26 West Martin Luther King Drive
Cincinnati, OH 45268
(513) 569-7877


Chief, Demonstration Section
John Martin
U.S. Environmental Protection Agency
Office of Research and Development
Risk Reduction Engineering Laboratory
26 West Martin Luther King Drive
Cincinnati, OH 45268
(513) 569-7758

The Demonstration Site

Joseph B. Healy, Jr.
U.S. Environmental Protection Agency
Superfund Remedial Branch (H-6-3)
Hazardous Waste Management Division
1235 Mission Street
San Francisco, CA 94103
(415) 777-3000
Director, Superfund Technology Demonstration
Division

Robert Olexsey
U.S. Environmental Protection Agency
Office of Research and Development
Risk Reduction Engineering Laboratory
26 West Martin Luther King Drive
Cincinnati, OH 45268
(513) 569-7861
                                              29

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           Appendix B
Vendor's Claims for the Technology
              31

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                       Appendix B Contents
                                                                Page
Introduction 	  34
Description of the ULTROX® Process  	  34
ULTROX® Equipment  	  35
Applications of the ULTROX® System  	  35
Selected Case Studies  	  39
Cost Information	  40
Summary 	  40
                                  32

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                              Figures
Number                                                       Page
   B-l    ULTROX® system flow diagram	   36
   B-2    Photograph of the ULTROX® unit	   37
                             Tables
B-2
B-3
B-4
B-5
B-6
B-7
Contaminants Treated by the ULTROX® System 	
Treatability and Design Study Results Using Pilot Plants On-Site
Applications of Full-Scale ULTROX® Systems 	
Direct Operation and Maintenance Costs Using UV
Radiation/Oxidation for Water Supplies
Direct Operation and Maintenance Costs Using UV
Radiation/Oxidation at Industrial Installations 	
Typical Capital Costs for UV Radiation/Oxidation Systems 	
38
38
39
41
41
42
                                33

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                                         Appendix B
                         Vendor's Claims for the Technology
Note: This appendix to the report is based upon
claims made by Ultrox International  either in
conversations or in written or published materials.
These claims and interpretations of the regulations
are those made by the vendor and are not necessarily
able to be substantiated by test  data. Many of
Ultrox's claims are compared in Appendix C with the
available test data.
Introduction

The removal of low levels of organic contaminants
from groundwaters and industrial wastewaters
presents a challenge to environmental professionals.
The ULTROX® (a registered trademark of Ultrox
International) ultraviolet (UV) radiation/oxidation
process is a cost effective treatment technique which
is applicable to the destruction of a wide range of
soluble organic contaminants in water. Other well-
known and commonly used treatment processes such
as granular activated carbon (GAG) and air stripping
transfer pollutants from one medium to another.
With increasing public and regulatory concern over
the fate  of pollutants,  such transferential
technologies are not optimal.

Conventional chemical oxidation has been used in
the treatment of various waters polluted by organic
chemicals for a  number of years. Potassium
permanganate, chlorine, and chlorine  dioxide have
been used for treating organics such as phenol and its
homologs in wastewaters. Hydrogen  peroxide, with a
catalyst such as ferrous sulfate, has been used for
oxidizing  phenol and  other benzene derivatives.
Processes utilizing iron-catalyzed peroxides and
chlorine compounds are attractive because they  use
relative low-cost treatment equipment. The
disadvantages of these processes are that they can
attack only a limited number of refractory organics,
and that they produce iron sludges or chlorinated
organics. Ozone alone has been used to treat phenolic
wastes, cyanides,  and certain pesticides.  Ozone
treatment is a very  clean process but is limited in the
number of compounds which it can effectively treat.

The  use of UV radiation-catalyzed  ozone plus
hydrogen  peroxide (UV radiation/oxidation) as a
water treatment technique is rapidly expanding.  It
offers a means of solving many of the problems
created by the water soluble, toxic organic chemicals
that are found today  in groundwater, wastewater,
leachate, and drinking water supplies without many
of the  disadvantages  of more  conventional
techniques.

UV radiation/oxidation, when used as a stand-alone
treatment process or  in tandem with a few of the
above mentioned processes, can cost-effectively
destroy the  organic chemicals on EPA's  priority
pollutant list or render the organics non-toxic.

This appendix describes the experience of Ultrox
International in developing  and applying the
ULTROX® UV radiation/oxidation process to the
full-scale  treatment  of organics in wastewaters,
drinking  waters, leachates, and  groundwaters.
Ultrox International was issued a process-patent  in
1988 covering the application of UV radiation, ozone,
and hydrogen peroxide to the treatment of a broad
range of organic compounds in water.
Description of the ULTROX® Process

The ULTROX® UV radiation/oxidation process was
developed over a 15-year period. UV radiation, when
combined with ozone and/or hydrogen peroxide,
produces  a highly oxidative  environment
significantly more destructive than that created with
ozone or hydrogen peroxide by themselves  or in
combination.

UV radiation significantly enhances ozone and
hydrogen peroxide reactivity by:

•  Transformation of ozone and hydrogen peroxide
   to highly reactive OH° radicals

•  Excitation of the target organic solute to a higher
   energy level

•  Initial attack of the target organic compound by
   UV radiation

The importance of the conversion of the ozone and
hydrogen peroxide to OH° can be  more easily
                                               34

-------
understood after studying the relative oxidation
power of oxidizing species. Hydroxyl radicals have
significantly higher oxidation power than either
hydrogen peroxide or ozone. The oxidation potentials
and relative oxidation powers of several oxidants are
as follows:
Species
Fluorine
Hydroxyl radical (OH°)
Atomic Oxygen
Ozone (O3)
Chlorine dioxide
Hydrogen peroxide (H2O2)
Perhydroxyl radicals
Hypochlorous acid
Chlorine
Oxidation
Potential Value
3.06
2.80
2.42
2.07
1.96
1.77
1.70
1.49
1.36
Relative
Oxidation
Power
(Cl = 1.00)
2.25
2.05
1.78
1.52
1.44
1.30
1.25
1.10
1.00
The effect of UV-enhanced oxidation is illustrated in
Table B-l.


ULTROX® Equipment

ULTROX® UV  radiation/oxidation equipment
treatment systems  have very few moving parts,
operate at low pressure,  require  minimum
maintenance, operate full-time or intermittently in
either a continuous or batch-treatment mode, utilize
efficient, low-temperature, long-life UV lamps, and
can employ the use of a microprocessor to control and
automate the treatment process.

The  ULTROX® UV radiation/oxidation system
consists of a UV radiation/oxidation treatment tank
and an oxidation source which can be either an ozone
generator with  an air  preparation system  or  a
hydrogen peroxide  feed system. Figures 2-1 (see
Section 2), B-l, and B-2 are an isometric assembly
view, a drawing, and a photograph, respectively, of a
model F-150 system, which accommodates flow rates
up to 10 gpm or batches of 150 gallons.

The  treatment tank is made of stainless steel. The
UV lamps are enclosed within quartz tubes for easy
replacement and are mounted vertically within the
tank. Depending upon the size of the tank and the
type of wastewater to be treated, the tank can have
four to eight chambers separated by baffles. Lamps
are installed either in all chambers or in designated
chambers, depending on the  treatment specified.
When ozone is used as the oxidant, it is introduced at
the base of the chamber. The ozone is dispersed
through porous stainless steel diffusers. The number
of diffusers needed will depend upon the type of
organics being oxidized and the degree of removal
required.
Ozone is produced from either compressed air, dried
to a -60°F dewpoint by desiccarit columns, or produced
from compressed or liquid oxygen. Up to 2 percent (by
weight) ozone is generated from air, and  up to 5
percent  (by weight) ozone  can  be produced
economically from oxygen.

Commercial-grade hydrogen peroxide used in the
process, is directly metered into the influent line to
the reactor.

Water pumped into the treatment tank flows from
chamber to chamber in a sinusoidal path. When the
reactor uses ozone, the residual ozone in the off- gas is
decomposed back to oxygen by the use of a fixed-bed
catalytic  unit operating at 150°F. The air is  then
vented to the atmosphere.

Ozone generators with varying capacities are  used
with the Model  F-150  reactor. The size of the
generator  depends  upon the ozone  dosage
requirements. Present installations use 28 to 140
pounds per day capacities.

Applications  of the ULTROX® System

The UV radiation/oxidation equipment developed by
Ultrox in recent years  has been used to treat a wide
variety of  waste streams. Table B-2 lists toxic
compounds found in wastewaters and groundwaters
that have  been  successfully treated with  the
ULTROX® system.  Specific case histories  of
treatability and design studies for private industries
and military installations are presented in Table B-3.
Contaminants oxidized included  pesticides,
petroleum  compounds, munitions waste,  and
chlorinated solvents. In each of these cases,  pilot
treatment plants were operated on-site to  develop
treatment design and cost data.

Table B-4 illustrates projects where the treatability
and design studies were converted into permanent
on-site UV radiation/oxidation installations. Full-
scale  ULTROX® units are currently treating
contaminated groundwater, wastewater, and process
water. Contaminants in these waters  include
phenols,  chlorinated  solvents, hydrazine,
dimethylnitrosamine,  tetrahydrofuran,  and
formaldehyde.  Commercial systems have been
designed, built,  and installed to treat flows varying
from 10,000 to 300,000 gallons per day. A system to
treat 1.3  million gallons per  day is under
construction.
Standard equipment designs are used in all of these
installations. Reactor size varies from 300  to 4,800
gallons. Ozone  generators range from 21 to 140
pounds per day. In several cases, hydrogen peroxide
is used in place of, or with, ozone.
Specific design  parameters are developed  through
performance of  treatability studies, pilot tests, and
                                               35

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Table 8-1. Oxidations of Methylene Chloride and Methanol
Contact Time
(min.) Control UV
Melhyleno Chloride
0 100 100
15 100 59
25 100 42
Mothanol
0 75 75
30 75 75
Notes: i.
2.
Ozone
from Ozot
Generate
UV
(ty
j
All concentrations reported in mg/L.
NDA = No data available.
Rotameter
(typical)
Needle Valve gl \Fjl Fj
(typical) bat |zjt m
rB 3 !} 4
>

Lamp 	 cx^^
pical) —• 	 o
o
o
O
Stainless °
Reactor
CD-1
J J
Headspace
o/ ^ o o o
o o o o
o o o o
r o o r o o
0 00 0
o o o o
o • • e
Ozc

Hydrogen Peroxi
Feed Tank
i ,

de
r'Ov
$
O
o
o
o
UV/H2O2 O3/H2O2 UV/O3 UV/O3/H2O2
100 100 100 100
46 32 36 19
17 21 16 7.6
75 " NDA 75 75
75 NDA 31 1.2
C
)zone Manifold Catalytic
.. / ,_. Ozone
1 H Decomposer
< •{ ^
erflow Weir
pical)
— __ ~S>-L^ —
\ o o o
o o o
0 O 0
0 , 0 0
O O 0
o o o
r Sight Glass
,00 0
o o o
o o o - 	 •'" 1 1
. I Treated
' . . * •„ I* I I U> Effluent
. . II Stora9e
^^ 1 	 9 Tank
r~hJ " 't><17~^
I
/ I
me Diffuser From Shallow 1
(typcal) I 	 Groundwater ^ 	 Effluent
^__| Monitoring Wells Sample Tap
XH-|-
Contaminated Water
 Figure B-1.  ULTROX® system flow diagram.
full-scale shakedowns. Treatability  studies are
carried out first in the laboratory using bench-scale
peroxide. If the results are encouraging, the next step
in the study involves the  installation of a skid-
equipment to evaluate the feasibility of treating the    mounted, pilot-scale unit on-site. Sufficient design
water with UV radiation/ozone,  UV radiation/    and cost data normally are collected within 2 weeks.
hydrogen peroxide, or UV radiation/ozone/hydrogen    Specifications for the full-scale system are then
                                                  36

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Figure B-2.   Photograph of the ULTROX® unit.
                                                      37

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Table B-2.  Contaminants Treated by the ULTROX® System
                 Industrial Effluent Contaminants
                                                                              Groundwater Contaminants
                 Amines
                 Analine
                 Benzene
                 Chlorinated solvents
                 Chlorobenzene
                 Complex cyanides
                 Creosote
                 Hydrazine compounds
                 Isopropanol
                 Methyl ethyl ketone (MEK)
                 Methyl isobutyl ketone (MIBK)
                 Methylene chloride
                 Polychlorinated biphenyl (PCB)
                 Pentachlorophenol
                 Pesticides
                 Phenol
                 Cyclonite (RDX)
                 2,4,6-Trinitrotoluene (TNT)
                 Toluene
                 Xylene
                 Polynitrophenols
                                         Benzene, toluene, and xylene (BTX)
                                         Bis (2-chloroethyl) ether
                                         Creosote
                                         1,2-Dichloroethane(1,2-DCA)
                                         Dichloroethylene (DCE)
                                         Dioxins
                                         Dioxanes
                                         Freon 113
                                         Methylene chloride
                                         Methyl isobutyl ketone (MIBK)
                                         Polychlorinated biphenyl (PCB)
                                         Tetrachloroethylene (PCE)
                                         Pentachlorophenol
                                         Pesticides
                                         Polynuclear aromatic hydrocarbons (PAH)
                                         1,1,1 -Trichloroethane (1,1,1-TCA)
                                         Trichloroethylene (TCE)
                                         Tetrahydrofuran (THF)
                                         Vinyl chloride
                                         Triglycol dichloride ether
Table B-3.  Treatabllity and Design Study Results Using Pilot Plants On-Site
           Customer
         Application
                                                                     Contaminants
                                                                                                     Results
 Bulk Chemical Transfer Depot
 Municipal Water Producers

 Aerospace Co.

 Chemical Co.

 Automotive Co.
 Electronics Co.


 Munition Plants

 Army Bases


 Semiconductor Co.


 Petrochemical Mfr.

 Semiconductor Mfr.
Contaminated groundwater
Contaminated drinking water
supply
Paint stripping wastewater

Wastewater

Contaminated groundwater
Wastewater/runoff, groundwater
Wastewater

Contaminated groundwater


Wastewater


Wastewater

Contaminated groundwater
TCE, PCE, methylene chloride

TCE, PCE, color


Methylene chloride


Misc. pesticides (including
DBCP)
TCE, Methylene chloride

PCBs, VC, DCA, and other
VOCs


TNT, RDX


DIMP, DBCP, VOCs



EDTA



Benzene


Benzene, toluene, ethylbenzene,
xylene
 Water treated and reinjected
 VOCs and color reduced to
 below state action levels
 Methylene chloride reduced from
 4,000 ppm to less than 100 ppb
 DBCP and other pesticides
 reduced to less than i ppb
 Reduced 10 ppm to 5.0 ppb
 Reduced PCBs to less than 1
 ppb; VOCs reduced to below
 state action levels
 TNT and RDX reduced from 100
 ppm to less than 1 ppm
 DIMP and DBCP reduced to less
 than 10 ppb; VOCs reduced to
 below state action levels
 Reduced EDTA from 6,000 ppm
 to 100 ppm
 (acceptable discharge standard)
 Reduced benzene from 10 ppm
. to 50 ppb
 Reduced contaminants from 14.0
 ppm to 4.0  ppb
Notes:

DCA: dtehtofoetnane; DBCP: dibromochloropropane; DIMP: diisopropyl methyl phosphonate; EDTA: ethylenediamine tetraacetic acid;  PCB:
Polychlorinated biphenyl; PCE: tetrachloroethylene;  RDX: cyclonite; TCE: trichloroethylene; TNT: 2,4,6-trinitrotoluene;  VC: vinyl chloride;
VOC: volatile organic compound.
prepared. Standard reactors, ozone generators, and
hydrogen peroxide feed systems are utilized. Systems
are assembled and  tested at Ultrox's facilities and
                               then shipped to  the job site.  The systems  are then
                               installed, inspected, and turned over to the customer.
                               Full-service maintenance contracts are available.
                                                           38

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Table B-4. Applications of Full-Scale ULTROX® Systems
         Customer
        Application
       Contaminants
                                                                                       Results
 Wood Treatment Plants (2)

 Closed Wood Treating Plant

 Chemical Plant


 Automotive Foundry
 Aerospace Co.

 Chemical Plant

 Semiconductor Co.
Wood treatment wastewater

Contaminated groundwater

Fume scrubber waste


Contaminated groundwater
Contaminated groundwater

Wastewater

Contaminated groundwater
Phenol, pentachlorophenol

Phenol, pentachlorophenol

Hydrazine, monomethyl
hydrazine, unsymmetrical
dimethyl hydrazine
TCE, 1,2-trans-DCE
TCE, TCA, DCA, PCE,
methylene chloride
Phenol, formaldehyde
THF
Treated water discharged to
POTW
Treated water discharged to
POTW
Destroyed parent compounds to
not detected levels and dimethyl
nitrosoamine below 10 ppb
Treated water discharged to lake
Treated water dsicharged to
POTW
Treated water discharged to
POTW
Replaced a GAC system to
reduce THF from 1,000  ppb to
less than 5 ppb
Notes:

DCA: dichloroethane; DCE: dichloroethylene; GAC: granular activated carbon; PCE: tetrachloroethylene; POTW: publicly-owned treatment
works; TCA: trichloroethane; TCE: trichloroethylene; THF: tetrahydrofuran.
Full-scale systems,  in most cases, are automated
using microprocessor control.  The system usually
requires periodic monitoring (once per shift or once
per day). The systems are designed to operate in a
batch or continuous mode depending on treatment
requirements.
In a number of cases, UV radiation/oxidation is used
as part of a treatment train. For example, at wood
treatment  sites, the wastewater or groundwater
requires breaking of oil/water emulsions, removal of
suspended matter, and adjustment of pH prior to the
UV radiation/oxidation treatment.

Selected Case Studies

Automotive Parts Manufacturer
Testing of  groundwater  at a Michigan automotive
parts manufacturing site revealed significant VOC
contamination. TCE levels of 5,000  to  10,000  ug/L
were recorded, as well as  trace  levels  of other
chlorinated solvents. The Michigan  Department of
Natural Resources required that the manufacturer
pump and treat the groundwater.

The manufacturer investigated air  stripping  with
GAC off-gas treatment, aqueous phase GAC, and
ULTROX® UV radiation/oxidation as  possible
treatment  alternatives. Bench-scale studies were
conducted at a GAC supplier and at  Ultrox's
laboratory. While all  treatment techniques could
provide the  required  removal levels,  UV
radiation/oxidation was the most economical. Testing
of an ULTROX® P-75  pilot-scale treatment system
over a 2-week period confirmed the data obtained in
the laboratory. An ULTROX® F-3900 treatment
                          system was ordered and installed in May 1989. The
                          system is currently operating and  achieving the
                          following results,  which  exceed  Michigan
                          requirements:
                                                          210 gpm
                                                          5,500 ug/L TCE
                                                          1 ug/L TCE
                                                          $/l.OOP gallons
                                                            $0.119
                                                              0.188
                                                              0.133
                                                              0.44
                                                              0.29
                                                            $0.73
 Flow Rate:
 Influent Concentration:
 Effluent Concentration:
 Treatment Costs:

   Ozone (@ 0.06/kWh)
   H2O? (@ $0.75/lb)
   UV (incl. power and
     annual  lamp
     replacement)
   O&M Cost
   Capital Amortization
     (16%/year)

   Total Treatment Cost:


 Semiconductor Manufacturer

 In 1982, groundwater contamination was detected
 beneath a Hewlett Packard facility in Palo Alto,
 California. The contamination was due to leaks in
 underground chemical  storage  tanks. Benzene,
 toluene, ethylbenzene, and xylene (BTEX) levels of
 4,000 to 15,000 ug/L were recorded.

 In 1988, granular activated carbon (GAC) treatment
 of groundwater was initiated as an interim measure.
 In early 1989, under the sponsorship of the California
 Department of Health Services Hazardous Waste
 Reduction Grant Program, Ultrox brought a mobile
 P-150 UV radiation/oxidation system to the site.
 During 3 weeks of testing, Ultrox  demonstrated the
 treatment equipment's  ability to  treat  the
                                                  39

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groundwater to publicly-owned treatment  works
(POTW) or NPDES standards. Treatment costs for a 5
gpm flow were $60,000 per year with  the GAC
system.  Based on the  field studies, projected
operation and maintenance (O&M) costs for an
ULTROX® system are less than $5,000 per year. The
treatment costs, scaled up to 50 gpm, to meet either
the POTW and NPDES standards are as follows:
Flow Rate:
Influent Concentration:
Effluent Concentration:
Treatment Costs:
Ozone (@0.06/kWh)
H2O? (@ $0.75/lb)
UV (incl. power and
  annual lamp
  replacement)
O&M Cost
Capital Amortization
  (16%/year)
Total Treatment Cost:
    50 gpm
    ll.OOOppbBTEX
    <5ppbBTEX
    $71.000 gallons
 98.66%
Removal
 BTEX

 $0.31
  0.28
  0.32
 99.96%
Removal
 BTEX
  $0.38
   0.38
   0.64
  0.91
   1.40

   0.91
  $2.31
Wood Treatment Facility
The groundwater under a closed wood treatment
facility in Nashua, New Hampshire, had widespread
contamination due to leaking storage tanks and past
disposal practices.  Contaminants included phenol
and POP. After extensive bench testing, the selected
treatment processes were filtration followed by
oil/water separation followed by UV radiation/
oxidation. An ULTROX®F-650 treatment system was
installed in April 1986 and has been operating on a
24 hour per day  basis  since then. Operating
conditions and treatment costs are as follows:
Flow Rate:
Influent Concentration:

Effluent Concentration:

Treatment Costs:
   Ozone (@ 0.06/kWh)
   UV (incl. power and
    annual lamp
    replacement)
   O&M Cost
   Capital Amortization
    (16%/year)
   Total Treatment Cost:
     40 gpm
     5 ppm phenol,
       100 ppb PCP
     < 0.1 ppm phenol,
       < 0.1 ppb PCP

     $/1.000 gallons

       $0.50


        0.35
        0.85

        0.75
       $1.60
Cost Information

Table B-5 represents the direct O&M costs for
treatment of contaminants in groundwater at water
supply sites. The costs are based upon pilot plant
studies at four different sites in Southern California.
At three of the sites, PCE and TCE were the
contaminants with concentrations ranging from 20 to
200 ppb.

Table B-6 presents costs for treatment of wastewater
and groundwater at various permanent industrial
installations. Costs are presented as dollars per 1,000
gallons treated. For hydrazines, a small volume of
water is  treated per day on a batch basis and a
comparatively long reaction time is needed. UV
radiation/oxidation was found to be the  most cost-
effective  method of destroying the three types of
hydrazines and the nitrosamine that is formed as a
by-product  of   the   oxidation.   The   UV
radiation/oxidation system  replaced a chlorination
unit,  which produced chlorinated  organic by-
products.

The price range of UV radiation/oxidation equipment
is presented in Table B-7. Capital costs for various
installations  vary  from $45,000  to  $300,000
(uninstalled). Costs depend on the oxidants required,
their estimated dosages, the chemical structure of the
organic compounds treated, the number of UV lamps
required, and the retention time required to achieve
an acceptable discharge.
             Summary

             Over the last 15 years, UV radiation/oxidation has
             progressed from research and  development to
             commercial operation. During these  years, Ultrox
             International has advanced its treatment system
             design through applied bench testing, pilot studies,
             and full-scale systems to remove contaminants from
             a wide variety of wastewaters and groundwaters. UV
             radiation/oxidation technology is not suitable for
             every organic  contamination problem. It can,
             however, effectively address a wide range of cleanup
             needs. This form of on-site chemical  oxidation can
             offer real advantages over conventional treatment
             techniques  and should be  considered  when
             evaluating water treatment alternatives.
                                               40

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Table B-5. Direct Operation and Maintenance Costs Using UV Radiation/Oxidation for Water Supplies
Type of Water
Contaminated potable
drinking groundwater
Contaminated potable
drinking groundwater
Contaminated potable
drinking groundwater
Contaminants
TCE, PCE
TCE, PCE
Color
Contaminant
Concentration
less than 20 ppb
200 ppb
70 color units
Discharge to
Drinking water supply
Drinking water supply
Drinking water supply
Direct O&M Cost Range
($/l,OOOgal)
0.10 to 0.20
0.20 to 0.30
0.10 to 0.1 5
Notes:  1. Assumes cost of electrical energy is $0.06/kWh.
       2. PCE: tetrachloroethylene; TCE: trichloroethylene
Table B-6. Direct Operation and Maintenance Costs Using UV Radiation/Oxidation at Industrial Installations
Type of Waste
Wood treatment
wastewater
Contaminated
groundwater
Scrubber wastes
Contaminated
groundwater
Contaminated
groundwater
Contaminated
groundwater
Wastewater
Contaminants
Pentachlorophenol
and phenol
Pentachlorophenol
and phenol
Hydrazine,
monomethyl-
hydrazinee,
unsymmetrical-
dimethylhydrazine
TCE, trans-DCE,
methylene chloride
TCE, TCA, DCA,
PCE, methylene
chloride, VC
THF
Phenol
Total Contaminant
Concentration
50 ppm
5 ppm
5,000 ppm
5 ppm
600 ppb
1 ppm
90 ppm
Discharge to
POTW
POTW
Biotreatment plant
on-site
Surface Water
POTW
Ground
POTW
Daily Volume Treated
(gpd)
30,000
86,400
600 to 1 ,500
300,000
72,000
216,000
4,300
Direct O&M Cost
Range ($/1 ,000 gal)
1.25-1.35
0.90-1.00
86.
0.47
0.33
0.39
6.48







Notes:  1. Assumes cost of electrical energy is $0.06/kWh.
       2. DCA: dichloroethane; PCE: tetrachloroethylene; POTW: publicly-owned treatment works; TCA: trichloroethane; TCE:
          trichloroethylene; THF: tetrahydrofuran; trans-DCE: trans-dichloroethylene; VC: vinyl chloride.
                                                             41

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Table B-7. Typical Capital Costs for UV Radiation/Oxidation Systems
Type of Waste
Wood treatment
wastewater
Contaminated
groundwater
Scrubber wastes
Contaminated
groundwater
Contaminated
groundwater
Contaminated
groundwater
Wastewater
Contaminants
Pentachlorophenol, phenol
Pentachlorophenol, phenol
Hydrazines
TCE, trans-DCE,
methylene chloride
TCE, TCA, DCA, PCE,
methylene chloride, VC
THF
Phenol
Total Contaminant
Concentration
150 ppm
5 ppm
5,000 ppm
5 ppm
600 ppb
1 ppm
90 ppm
Water Flow Rate (gpd)
30,000
86,400
600-1,500
300,000
72,000
216,000
4,300
Price Range (uninstalled)
($)
125,000-150,000
175,000-200,000
125,000-150,000
225,000-275,000
130,000-150,000
250,000-300,000
45,000-55,000
Notes:  1. Assumes cost of electrical energy is $0.06/kWh.
        2. DCA: dichloroethane; PCE: tetrachloroethylene; TCA: trichloroethane; TCE: trichlqroethylene; THF: tetrahydrofuran; Trans-DCE:
          trans-dichloroethylene; VC: vinyl chloride.
                                                              42

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       Appendix C
Site Demonstration Results
           43

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                        Appendix C Contents
                                                                   Page
Introduction	  46
Site Characteristics	  46
Waste Characteristics  	  47
Review of Technology and Equipment Performance  	  48
Review of Treatment Results 	  51
References  	  53
                                   44

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                                 Figures
Number
   C-1    Lorentz barrel and drum site location
   C-2    General geologic cross-section 	
Page
 47
 48
                                Tables
   C-l    Performance Data for Reproducible Runs  	   51
                                    45

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                                         Appendix C
                               Site Demonstration Results
Introduction

In 1947, Lorentz Barrel and Drum (LB&D) began
recycling drums at its facility in San Jose, Santa
Clara County, California. Other industrial uses at
the site  included auto wrecking,  roofing and
construction, sandblasting,  and auto junkyard.
Drums for recycling were received from over 800
private companies, as well as military bases,
research laboratories, and county  agencies in
California and Nevada. These drums generally
contained residual aqueous wastes, organic solvents,
acids, metal oxides, and oils.

As part of normal operations at the site, residual
wastes from drums and wastewaters from cleaning
drums were disposed of in an on-site drainage ditch.
From the ditch, these wastes were routed to a large
sump located in the northeast corner of the site. Prior
to 1968, wastewater from the sump was discharged to
the storm drain system. Sometime between 1968 and
1971, the discharge was diverted to the sanitary
sewer. This practice was discontinued  between 1983
and  1984;  subsequently, liquid wastes  were
reportedly reduced in volume by evaporation and
then drummed and disposed of off-site as hazardous
waste (Ebasco, 1988).

In 1987, LB&D ceased operation at the site due to a
temporary restraining order from the Santa Clara
County District Attorney's Office. Later, the U.S.
EPA (Region IX) assumed lead agency responsibility
for site remediation and  initiated a remedial
investigation/feasibility study.

The  material presented  in this appendix briefly
summarizes  the work performed during the SITE
demonstration and the results presented in the
Technology Evaluation Report (EPA, 1989).


Ultrox Technology Evaluation and the SITE
Program
The  Ultrox UV radiation/oxidation technology was
evaluated by Region IX as part of the engineering
evaluation/cost analysis of remedial alternatives and
through a treatability study. The treatability study
was successful in demonstrating that the technology
could treat the contaminated groundwater at the
LB&D site (Ebasco, 1988).

Ultrox International submitted a proposal  under
EPA's SITE Program to  demonstrate the Ultrox
technology at the LB&D facility. Because of the
promising results of the treatability study, and
because  Region IX  needed  additional data to
complete its decision-making for Phase I remediation
of groundwater at the site, the Ultrox technology
demonstration was put on an accelerated schedule.
The  field demonstration was  conducted  from
February 24 through March 9,1989.

Site Characteristics

When LB&D  began operating, the site comprised
10.5 acres (Figure C-l).  Since then,  half of the
original property has been sold, resulting in the
current L-shaped site which covers 5.25 acres. This
area is suspected to contain  the  highest levels of
contamination. The site is surrounded  by a chain-
link fence to prevent unauthorized access.

The site  slopes gently from the  southwest to the
northeast corner. The highest  elevation at the
southwest corner is 106 feet, aruLthe lowest point at
the northeast corner is 102 feet above mean sea level.

The water table at the site is approximately 20 feet
below ground surface (Figure C-2).  The actual
aquifer thickness, seasonal water table fluctuations,
and the hydraulic characteristics of the clay aquitard
are unknown.  As is typical with water table aquifers,
the shallow groundwater flow appears to follow the
ground surface topography, flowing northeast toward
Coyote Creek, a local watercourse, less than 1/2 mile
east of the site.

The climate in the area is characterized by warm, dry
summers and cool, wet winters. Annual minimum
temperatures  are generally a few degrees  below
freezing,  while maximum  temperatures in excess of
100°F are common. Normal January and July daily
average  temperatures  are  49.5°F and 68.8°F,
respectively. The temperature at the site during the
demonstration varied from the  upper 50°F to  upper
60°F range. Normally, average annual rainfall  in the
                                               46

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                          •VJ
                            San Jose
                           Muni Baseball
                            Stadium
 Figure C-1.  Lorentz barrel and drum site location.
area is 13.9 inches, most of which occurs from
November through April. During the last few days of
the demonstration, there was intermittent rainfall at
the site.


The LB&D  site is located in an  area  zoned for
manufacturing, at the southwest corner of East Alma
Avenue and South Tenth Street. The site is located
just south of land  zoned as residential. This
residential zone includes San Jose State University's
(SJSU) football stadium (Spartan Field and Spartan
Stadium) and recreation fields, as well as  the San
Jose Municipal Baseball Stadium. SJSU University
student housing (the closest residential area) is
located about a quarter mile north of the site.

Surface water runoff from the LB&D site is routed to
Coyote Creek via a 60-inch diameter storm drain at
the corner of East Alma Avenue and South Tenth
Street. This drain flows to Coyote Creek under Alma
Avenue. A secondary 18-inch storm drain runs
northwest under South Tenth  Street and connects
with the 60-inch diameter storm drain.

Coyote Creek flow rates are regulated by the Coyote
and Anderson reservoirs. An average flow rate of 45
cubic feet per second (cfs) has been recorded between
1970 and 1983. A maximum flow rate of 5,000 cfs was
recorded in March 1983.  Zero flow rate has been
recorded for short durations in the fall.
Waste Characteristics

The drum recycling operations over a 40-year period
are the principal causes for the site's contaminated
groundwater. Remedial investigations carried out by
state and Federal agencies from 1983 to 1987 have
indicated that the soils and the shallow groundwater
at the LB&D site are contaminated with VOCs,
pesticides, PCBs, and metals. These investigations
have also indicated that groundwater downgradient
of the site is contaminated with VOCs (Ebasco, 1988).
The organic contaminants measured in the on-site
groundwater  from 1983 to 1987  range  in
concentration from 0.2 ppb for chlordane, a pesticide,
to 2,108 ppb for TCE, a VOC. Organic contaminants
measured in the off-site groundwater range from 0.5
ppb for chloroform to 311 ppb for TCE (Ebasco, 1988).

Remedial activities at the site addressing soil
contamination have involved the excavation of four
major "hot spot" drainage and sump areas. Activated
carbon adsorption and UV radiation/oxidation
treatment technologies  were evaluated to clean  up
the groundwater. Since the Ultrox technology is best
suited for destroying dissolved organic contaminants,
such as  chlorinated hydrocarbons  and aromatic
compounds,  found in groundwater or wastewater
with low levels of suspended  solids, the  shallow
groundwater at the LB&D site was selected as the
waste stream to demonstrate the Ultrox technology.
Groundwater Sampling for the SITE
Demonstration
In anticipation of the SITE  demonstration,
groundwater samples were  collected in December
1988 from wells at and near the LB&D site. Samples
were collected from three off-site wells and two on-
site  wells near the location of the technology
demonstration. Several VOCs detected at relatively
high  levels  included acetone (160  ppb);  1,1-
dichloroethylene   (180    ppb);   1,2-trans-
dichlorqethylene (200 ppb); TCE (920 ppb); and vinyl
chloride (240  ppb). VOCs detected in all five wells
included  1,1-dichloroethylene;  1,2-trans-
dichloroethylene; 1,1,1-trichloroethane (1,1,1-TCA);
and TCE. No semivolatiles, PCBs, or uncharacterized
pollutants were detected. Based on these results, four
extraction wells were installed in the northeastern
corner of the  site to  collect contaminated
groundwater for the SITE demonstration.

During the demonstration, influent samples collected
during the test runs  were analyzed to characterize
groundwater contamination and measure removal
efficiencies.  Laboratory analytical parameters
measured during the  test runs  included the
following: VOCs, TOG, metals, semivolatiles, PCBs,
and pesticides. Field testing parameters included pH,
alkalinity, conductivity, temperature, and turbidity.
                                               47

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          110—1
         100—
          90—
       zs-  80 —
       •8
       5
       -J  70-
       CO
       CD
                            Water Level •
                             Oct. 1986
                                    Clay and Silt
          60 —
          50 —
          40—
          30 —
          20—'
Figure C-2. General geologic cross-section.
  Scale
H:1" - 50'
V: 1" = 10'
                                                                  Clay
                                                                       Sand and Gravel
The groundwater was contaminated primarily with
VOCs such as TCE and vinyl chloride, at levels of 100
and 40 ug/L, respectively.  Other VOCs present  at
relatively low concentrations (in the range of 5 to  15
ug/L)  included 1,1-dichloroethane (1,1-DCA), 1,1,1-
TCA, 1,2,-dichloroethane (1,2-DCA), benzene,
chloroform, and tetrachloroethylene. No PCBs,
semivolatiles, or  pesticides were detected in the
influent. During the demonstration period, there was
a 30 to  50 percent decrease in the influent VOC
concentrations. This decrease was probably due  to
VOC volatilization, although bladder tanks were
used to minimize the VOC losses.

The TOG concentration of the groundwater was about
25 mg/L. However, the concentration  of priority
pollutants (VOCs and semivolatiles) was only about 2
percent of the TOG concentration.

During the demonstration, the pH and alkalinity of
the groundwater were about 7.2 and 950 mg/L  as
CaCOs,  respectively. These measurements indicated
that the bicarbonate  ion (HCO3"), which acts as  an
                              oxidant scavenger, was present at high levels. Other
                              oxidant scavengers such as bromide, cyanide, and
                              sulfide were not detected. Since the  Ultrox
                              technology is based on an oxidation process, any
                              other species present in the contaminated  water
                              which consume  oxidants  were  viewed as an
                              additional load for the system.

                              Review of Technology and Equipment
                              Performance

                              The technology demonstration was divided into three
                              phases: (1) site preparation (approximately 3 weeks),
                              (2) technology demonstration (approximately  2
                              weeks), and (3) site demobilization (approximately 3
                              weeks). The activities and a review of technology and
                              equipment performance during these phases are
                              described below.


                              Site Preparation
                              Site preparation included setting up major support
                              equipment, on-site support services, and utilities.
                                               48

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These activities and equipment requirements are
described as follows.

To  accommodate the demonstration program
schedule,  Region IX installed four  groundwater
extraction wells at the LB&D site in January 1989.
The wells were  necessary to  obtain sufficient
groundwater from the most contaminated area of the
LB&D site for the technology demonstration  test
runs. Once installed and developed, the four wells
were pumped to estimate groundwater yields.

From February 20 to 23, 1989, approximately 13,000
gallons of contaminated groundwater from the LB&D
site  were collected from the extraction wells. Only
three of the four wells installed were needed to obtain
the necessary groundwater for the demonstration.

Major Support Equipment
Two 7,500-gallon bladder tanks were used to hold the
groundwater collected from the site. These  tanks
were flexible and made of a synthetic material
suitable for potable water storage. The bladder tanks
were selected to minimize VOC losses during the test
period.

Three dedicated, submersible pumps were used to
pump the  groundwater into the bladder tanks.  The
maximum and  average pumping rates  were
approximately 5 and 1 gpm per pump, respectively.
The bladder tanks and pumps were connected using
piping manifolds so that both tanks could be filled
simultaneously.  From the bladder tanks,  the
groundwater was pumped to the Ultrox unit.

A commercial-size (150-gallon) Ultrox unit, Model
PM-150, was delivered by  truck van.  This unit has
four skid-mounted modules designed for transport
with either a flatbed truck or in an enclosed trailer.
The unit was unloaded using a fork lift on February
21,1989.

A 21,000-gallon storage  tank was used to store
effluent from the Ultrox system. The tank was steam
cleaned prior to delivery  to the site. In addition,
several 55-gallon, open-top drums were used to store
wastewater generated during the sample collection
activities, laboratory analyses, and  decontamination
procedures.
On-Site Support Services
On-site laboratory analyses were conducted in a field
trailer. The field trailer also served as an office for
field personnel, provided shelter and  storage for
small equipment and supplies, and acted as a base for
site security personnel.  Two chemical toilets were
located near the trailer.
Although the LB&D site perimeter is enclosed by a
fence, a commercial security service was hired to
provide additional protection  from equipment
vandalism during evening hours and weekends.


Utilities

Utilities  required  for  the  Ultrox  system
demonstration included telephone, water, and
electricity service. A single telephone line was
installed  in the trailer. Telephone service was
required to order supplies, coordinate site activities,
and provide communication. Tap water was required
for equipment and personnel decontamination.
Water  used  for equipment and personnel
decontamination was provided using existing site
pipelines.

Electrical service was connected to the site from a
public utility. Electricity was required to operate the
Ultrox system, the office trailer, and the laboratory
equipment. The Ultrox system required 480-volt, 3-
phase electrical service, which was provided through
a 100-amp service using a  dedicated meter and a
transformer. An additional 110-volt, 100-amp service
was connected to another dedicated meter to provide
power to the office and laboratory trailer.


Technology Demonstration
Approximately 13,000 gallons of contaminated
groundwater were treated by the Ultrox system in 13
test runs over a 2-week period, with 1 or 2 test runs
performed each day. During this period, there were
no  significant variations from  the  proposed
demonstration schedule.  This  section discusses
operational and equipment problems and health and
safety  issues  associated  with the  SITE
demonstration.
Operational Problems

During the course of the field demonstration, two
operational problems with the electrical power
supply were encountered. These problems were a
wiring  problem discovered during Run  2 which
affected electricity measurements and an electrical
power shutdown at the end of Run 9, which was
caused by a minor accident at the site.

During Run 2, it was discovered that both the trailer
and the Ultrox system were insidvertently wired to a
common meter. As a result,  separate watt-hour
meters and service panels were installed for the
Ultrox system and the on-site  trailer.  An electrical
subcontractor  rewired and set  each meter properly,
and the electrical energy consumption for  the first
two runs was estimated by analyzing the power
consumed on subsequent runs. Based on the
electrical energy consumption observed in Runs 3 to
                                                49

-------
13, the electrical energy consumption by the trailer
appeared to be negligible.

At the end of Run 9, a trailer truck entered the site
and accidentally broke the wooden power pole that
supported the electric power lines by catching the
sagging lines with the trailer. Although the accident
did not cause any injury to the people working on-site
or damage  any equipment, as a precautionary
measure, the power was shut off, and the electrical
subcontractor was contacted to install a new power
pole.  A stronger pole was installed and power
restored the following morning.

To circumvent this accident, electrical lines could
have been buried at the site. Although the cost of the
demonstration would have increased, a safer work
atmosphere would have been  provided.  As  an
alternative,  the lines could have been placed clear of
any possible transportation routes or elevated to a
height necessary to accommodate truck  clearance.
Portable electrical generators could also have been
provided as a backup.


Equipment Problems
During normal  operations, the  Decompozon unit,
which is equipped with  a heater, is .designed to
destroy ozone in the reactor off-gas. After Run 8,
however, the heater malfunctioned. As a result, the
temperature in the unit,  which should normally be
140°F for the unit to function properly,  was about
80°F. The effect of this heater failure is reflected in
the ozone concentrations in the  Decompozon unit
exhaust For Runs 1 through  8  there was  greater
than 99.9 percent ozone destruction,  and ozone
concentrations in the exhaust were quite low (<0.1
ppm). However, ozone concentrations in the exhaust
were approximately  1 ppm for Runs 9 and  10, and
greater than 10 ppmfor Runs 11,12, and 13.

At its permanent installations, Ultrox incorporates
interlocks for emergency automatic shut-off of the
treatment unit if the heater fails so that operating
personnel will not be exposed to ozone even for short
periods. This feature should be incorporated at other
similar demonstrations.


 Health and Safety Considerations
 Work zones  were established  to minimize  the
 transfer of  hazardous materials and contaminated
 debris from potentially contaminated areas to "clean"
 areas at the site.  For the  demonstration,  the
 contaminant reduction zone was combined with the
 exclusion zone. The work zone contained the Ultrox
 system and associated equipment, power connections,
 55-gallon drums used to separately store wastewater
 and  contaminated  debris, the two  7,500-gallon
bladder tanks, and the 21,000-gallon steel storage
tank used for effluent wastewater storage.

In general,  health hazards associated with  the
demonstration resulted from exposure to  the
contaminated groundwater. Although the treatment
system was entirely closed, the potential routes of
exposure during the demonstration were inhalation,
ingestion,  and skin and eye contact from possible
splashes or spills during sample collection.

All personnel working in this  area had, at a
minimum, 40 hours of health and safety training and
were under routine medical surveillance. Personnel
were required to wear protective equipment
appropriate for the activity being performed. Steel-
toed safety boots were required in the exclusion zone.
Personnel  working in direct contact with
contaminated groundwater wore modified Level D
protective equipment, including safety shoes, latex
inner gloves, nitrile or Viton outer gloves, and safety
glasses.
 Equipment Demobilization
 Groundwater remaining in the bladder tanks after
 the final test run was treated by the Ultrox system
 and pumped to the effluent storage tank. Similarly,
 miscellaneous liquid wastes which had been stored in
 55-gallon drums during the test period were treated
 by the Ultrox system and pumped to the storage tank.
 These miscellaneous liquids  consisted of well
 development water, excess sample  volumes
 generated during sampling operations, and  spent
 chemical reagent wastes produced from on-site
 laboratory analyses.

 All effluent was temporarily stored in the tank prior
 to discharge. After the  effluent was analyzed to
 ensure that it met the applicable NPDES standards,
 it was discharged into a storm drain which emptied
 into Coyote Creek, a nearby waterway. All collected
 effluent was  held for approximately 2 weeks before
 discharge, awaiting laboratory test results.

 Contaminated materials, such as empty sample
 containers,  laboratory wastes, and disposable
 protective  equipment  generated during  the
 demonstration, were placed in a 55-gallon, open-top
 drum. These materials  contained only residual
 contamination. During the demobilization phase, the
 wastes  were packaged and stored  before  being
 disposed of off-site by Region IX.

 The Ultrox unit was loaded on a trailer truck  and
 transported to another site to treat contaminated
 groundwater.
                                                 50

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Review of Treatment Results

The demonstration was designed to evaluate the
Ultrox technology by controlling the system's five
operating parameters: hydraulic retention time,
ozone dose, hydrogen peroxide dose, UV radiation
intensity, and influent pH level. During the test
runs, these operating parameters were varied and the
system's performance was evaluated under each
resulting set of operating conditions.

VOCs were selected as the critical parameters for
evaluating the effectiveness of the Ultrox technology,
because the  Ultrox technology was developed
primarily to treat organics (such as VOCs,
semivolatiles,  and PCBs/pesticides). Of these
organics, only VOCs were found in the groundwater
samples collected in December 1988. As such, the
performance of the Ultrox system for each test run
was evaluated based on its effectiveness at removing
indicator VOCs.

The three indicator VOCs selected  were TCE, 1,1-
DCA, and 1,1,1-TCA. TCE was selected because it is
a major volatile contaminant at the site, and the
latter two VOCs were selected because, from Ultrox's
experience, they are relatively difficult to oxidize.
Only three indicator VOCs were selected because of
analytical time constraints to perform the tests over
the 2-week period. Full  VOC analyses were also
performed for all test  runs following completion of
the demonstration.

To assess the  effectiveness of the technology
performance,  the concentration  of total VOCs was
estimated by  adding the concentration of each VOC.
Since this study only uses the total VOC data for
qualitative  interpretation, this approach is
considered practical and useful from an engineering
perspective.

"Preferred" Operating Conditions
As part of the technology demonstration, the system's
performance during Runs 1 through 11  was
evaluated to determine "preferred" operating
conditions,  given the nature  of  contaminated
groundwater  at the site. For the Ultrox technology
demonstration, the "preferred" operating conditions
were  defined as the set  of operating parameters
where the effluent concentrations of indicator VOCs
were below their respective NPDES limits and the
relative operating costs were the lowest.

The initial operating conditions selected for Run 1
were expected to approximate optimum operating
conditions, based on the results of the groundwater
treatability study.  From Run 1, the selection of
operating conditions for Runs 2 to 11 proceeded in an
interactive manner, with the results of previous runs
setting operating conditions for subsequent runs.
To set operating conditions for subsequent runs, the
results from the overnight analysis of one-third of the
previous run's samples were evaluated. Specifically,
only two of the six replicate samples collected at each
of the three  liquid sampling locations  (influent,
midpoint, and effluent of the reactor) were analyzed
overnight by gas chromatography (GC), for the three
indicator VOCs. Only one-third of the samples could
be analyzed overnight, due to analytical time
constraints.

Based on the analyses of two replicate VOC samples
for each of the first 11 runs, only Runs 8 and 9 had
average effluent concentrations  of indicator VOCs
that were  below their respective NPDES limits. Of
Runs 8  and 9, a lower hydrogen peroxide dose  was
used in  Run 9. As a result, the operating conditions
for Run 9 were determined  to  be the "preferred"
operating  conditions. These conditions included a
hydraulic retention time of 40 minutes, ozone dose of
110 mg/L, hydrogen peroxide dose of 13 mg/L, all 24
UV lamps (at 65 watts each) operating, and influent
pH of 7.2 (unadjusted).

Subsequently, Runs 12 and 13 were performed using
the "preferred" operating conditions determined from
Run 9. The results from these latter two test runs
were used to evaluate if performance levels were
reproducible.  A summary  of the results  for
reproducible runs is presented in Table C-l.
Table C-1. Performance Data for Reproducible Runs

Run 9
TCE
1,1 -OCA
1,1,1-TCA
Total VOCs
Run 12
TCE
1,1 -DCA
1,1,1-TCA
Total VOCs
Run 13
TCE
1,1 -DCA
1,1,1-TCA
Total VOCs
Mean
Influent
(H9/L)

65
11
4.3
170

52
11
3.3
150

49
10
3.2
120
Mean
Effluent
(yg/L)

1.2
5.3
0.75
16

0.55
3.8
0.43
12

0.63
4.2
0.49
20
Percent
Removal

98
54
83
91

99
65
87
92

99
60
85
83
After the demonstration, complete analyses of all
replicate  samples from the 13  test runs were
performed.  From  these  results, the mean
concentration of 1,1-DCA in the effluent of Run 9 was
actually found to be slightly higher than 5 ug/L, the
discharge standard for the compound. However, these
                                                51

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results  were  not available until  after the
demonstration. Operating conditions for Run 9 are
still considered to be "preferred" since the mean
effluent  concentration was quite close  to  the
discharge standard.


Quantifiable Results
The Ultrox process achieved removal efficiencies
(RE) as high as 90 percent for the total VOCs present
in the groundwater at the LB&D site. Based on the
data for individual VOCs, REs for TCE were greater
than 99 percent, and REs for 1,1-DCA and 1,1,1-TCA
were as high as 65 and 85 percent, respectively.

The REs for the  three  indicator VOCs were
dependent on the operating conditions. For example,
the REs  for the  three indicator VOCs generally
decreased considerably in Run 7. This decrease was
most likely due to the decreased ozone dose  in that
run.

In Runs  9, 12, and 13, which were all run at the
"preferred" operating conditions, the REs for each
indicator VOC did not differ. That is, the technology
performance levels were reproducible under the same
operating conditions. In general, the REs for TCE
were higher than those for 1,1-DCA and 1,1,1-TCA.
This is expected, since 1,1-DCA and 1,1,1-TCA were
selected  intentionally because they are relatively
difficult to oxidize.

A comparison of the 95 percent upper confidence
limit (UCL) values for effluent VOC concentrations
in Runs  12 and  13 with the discharge standards
indicated that the effluent met the discharge
standards for all regulated VOCs. However, in Run 9,
the effluent did not meet the discharge standards for
1,1-DCA  and  1,2-DCA.  This  difference  in
performance among Runs 9,  12, and 13 is negligible
and may be attributed to the higher influent VOC
concentrations in Run 9 than in Runs 12 and  13.
Since the mean effluent VOC concentrations of 1,1-
DCA and 1,2-DCA are higher than the discharge
standard, statistical inferences at other confidence
levels (such as 90 percent) will not be different.


VOC Removal Due to Stripping
The potential for  VOC removal due to stripping was
evaluated since ozone gas was bubbled through  the
groundwater treated by the Ultrox system. The VOC
air sampling data indicated  that  stripping
contributed  significantly  to the total  removal,
(chemical oxidation plus stripping) of 1,1,1-TCA and
1,1-DCA. Specifically, stripping accounted for 12 to
75 percent of the total removals for 1,1,1-TCA, and
for 5 to 44 percent of the total removals for 1,1-DCA.

For compounds such as TCE and vinyl chloride,
stripping accounted for less than  10 percent of the
total removal, as oxidation was found to be the major
removal mechanism. For other VOCs such as 1,1-
dichloroethylene, 1,2-dichloroethylene, benzene,
acetone, and 1,1,2,2-tetrachloroethane, stripping was
negligible since only occasional traces  of these
compounds were detected in the_off-gas.


Final Products of the Treatment Process
The  developer claims that  the final products of the
oxidation of organic compounds in water are salts,
water, carbon dioxide, and possibly some organic
products. However, during the demonstration, no
significant TOC removals were achieved in  the
treatment system,  which implies that only  partial
oxidation occurred; as such, the predominant final
products were not carbon dioxide and water. In
addition, since no new VOCs were found by GC and
GC/mass spectrometry (MS) analysis of the effluent,
the final oxidation products do not appear to be new
VOCs. Instead, the final products may be organic
acids, which were analyzed as TOC in the TOC
analysis. Neither semivolatiles nor PCBs/pesticides
were detected in the effluent. Consequently,  the
Ultrox unit did not generate any of these compounds.

Metals such as iron and manganese were detected in
the influent at low concentrations. After treatment,
no significant metal removal was observed.


Field Parameters
Field parameters  measured during the test runs
included pH, alkalinity, conductivity, temperature,
and  turbidity. The effect of the treatment process on
field parameters are described below.

The  pH increased by 0.5 to 0.8 units after treatment.
The  pH increase indicates that partial oxidation of
organics occurred to produce organic acids and that
complete oxidation to CO2 did not occur, which would
result in a pH decrease. However, the pH increase is
not  surprising because the groundwater  had  high
alkalinity and an initial pH of about 7.2, at which the
predominant form of alkalinity was bicarbonate. The
reaction of hydroxyl radicals with bicarbonate or
carbonate ion yields hydroxyl ions (Hoigne  and
Bader, 1975). The production of hydroxyl ions due to
this reaction would have caused an increase in pH.
No  change in alkalinity  was observed after the
treatment.

The temperature increased by approximately 2  to 3
degrees Celsius after  the treatment.  This increase
was mainly due to the heat from the UV lamps and
not  the  oxidation  of  organics,  because  the
temperature  increase was higher than usual when
the  hydraulic retention time was increased from 40
minutes to 1 hour (Run 5), and the increase  was not
observed in Runs 10 and 11 when the UV lamps were
used in only three chambers.
                                                52

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Turbidity usually increased by 1 to 4 units (NTU)
after the treatment. This slight increase in turbidity
may be due to the limited removal of metals by metal
oxidation and precipitation.  No  change  in
conductivity was observed after the treatment.


Performance of the Decompozon Unit
The Decompozon unit destroyed ozone in the Ultrox
reactor off-gas to  levels less than 0.1 ppm  (OSHA
standards). The ozone destruction efficiencies were
observed to be greater than 99.99 percent.

Although the primary function of the Decompozon
unit is to remove ozone, significant VOC removals
occurred in the Decompozon unit when it functioned
as designed (Runs 1 through 8)..Specifically, volatile
organics present in reactor off-gas at levels of
approximately 0.1 to 0.5 ppm were reduced to below
detection levels in the Decompozon unit before air
was discharged to the atmosphere.

Electrical Energy  Consumption

The average electrical energy consumption during
the demonstration was about  11  kWh/hour of
operation. It was  noted that the electrical  energy
consumption was  higher in Run 7 (38 mg/L ozone
dose) than that in Run 6 (110 mg/L ozone dose), which
is  contrary to  what would  be expected. This result
cannot be explained.


Accomplishing the Goals of the Technology
Demonstration
In addition to meeting the  general objectives of the
SITE Program during  the Ultrox technology
demonstration, four specific goals were identified to
serve the needs of both the SITE Program and Region
IX. These four goals, and an evaluation of how they
were met, are discussed as follows.
1.  Demonstrate the ability of the Ultrox system to
   treat VOCs present in the groundwater at the
   LB&D site.

   The Ultrox system successfully treated VOCs
   present in the groundwater at the LB&D site to
   meet regulatory discharge standards. REs as
   high as 90 percent were achieved for  the total
   VOCs present in the groundwater at the LB&D
   site. Specifically, for the three indicator VOCs,
   REs for TCE were greater than 99 percent,  and
   REs for 1,1-DCA and 1,1,1-TCA were as high as
   65 and 85 percent, respectively.

2.  Evaluate the efficiency of the ozone decomposer
   unit in treating ozone in the reactor off-gas.
    The Decompozon unit destroyed ozone in the
    Ultrox reactor off-gas to levels less than 0.1 ppm
    (OSHA standards). The  ozone destruction
    efficiencies were observed to  be greater  than
    99.99 percent.

3.  Develop capital and operating costs for the Ultrox
    system that can be  used in Superfund decision-
    making processes at other sites.

    The cost of conducting the Ultrox technology
    demonstration was approximately $633,000. This
    cost includes  site characterization  and
    preparation, demonstration planning and  field
    work, chemical analyses, and report preparation.
    The developer's portion of this  cost was $23,000
    and the balance of $610,000 was allocated to the
    SITE Program. The cost of the Ultrox unit used in
    the demonstration was approximately $140,000.

4.  Develop information useful to Region IX for site
    remediation.

    The SITE  demonstration provided additional
    data that will assist Region IX  in completing its
    decision-making for Phase I remediation of
    groundwater at the LB&D site. Specifically, as a
    result of the demonstration, the contaminated
    groundwater was further characterized, and
    actual information regarding the "preferred"
    operating parameters for the Ultrox system was
    obtained.
References

Ebasco Services, Inc., 1988. Various reports on the
    Lorentz Barrel and Drum Site,  San Jose,
    California, work performed for EPA under REM
    III Program, Remedial Planning Activities at
    Selected Uncontrolled Substance Disposal Sites.

EPA, 1989. Technology Evaluation Report, SITE
    Program  Demonstration of  the  Ultrox
    International Ultraviolet Radiation!Oxidation
    Technology, EPA/540/A5-89/012.

Hoigne, J., and H. Bader, 1975. Ozonation of Water:
    Role  of Hydroxyl Radicals  as  Oxidizing
    Intermediate's, Science, 190,782:784.

PRC Environmental Management, Inc., 1989. Final
    Report,  SITE Program Demonstration Plan for
    the Ultrox International UV Radiation/Oxidation
    Process, prepared  for U. S. Environmental
    Protection Agency, Office  of  Research  and
    Development and Office  of Solid Waste  and
    Emergency Response.
                                               53

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 Appendix D
Case Studies
     55

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                         Appendix D Contents
                                                                       Page

Introduction	   58
Case Study D-l, Department of Energy, Kansas City Plant, Missouri  	   58
    Introduction  	   58
    Plant Description  	   58
    Methodology 	   59
    Results	   59
    Conclusions and Recommendations  	   60
Case Study D-2, Hewlett Packard Facility, Palo Alto, California 	   60

    Introduction  	   60
    Plant Description  	   60
    Methodology 	60
    Results 	   62
Case Study D-3, FEI Microwave, Sunnyvale, California  	   63
    Introduction  	   63
    Plant Description  	   64
    Methodology 	• • •   64
    Results 	   64
Case Study D-4, Golf Course, City of South Gate, California  	   65

    Introduction  	   65
    Results 	   66
Case Study D-5, Xerox Facility, Webster, New York 	   66

    Introduction 	   66
    Plant Description  	   68
    Methodology 	   68
    Results 	   68
Case Study D-6, Koppers Industries, Denver, Colorado  	   68
    Introduction	   68
    Results 	   68
Case Study D-7, General Electric Company, Lanesboro, Massachusetts	   69

    Introduction 	   69
    Plant Description  	   69
    Methodology 	   69
    Results 	  69
References 	  69
                                      56

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                                   Tables
Number                                                               Page
  D-l-1    Groundwater Treatment Plant Monitoring Plan,
          Flow-Through Mode 	  59
  D-l-2    Groundwater Treatment Plant, Batch Results  	  60
  D-l-3    Groundwater Treatment Plant Flow Data  	  60
  D-l-4    Groundwater Treatment Plant Total Inorganic Halogen Results  ...  61
  D-l-5    Groundwater Treatment Plant VOC Results  	  61
  D-2-1    Groundwater Quality Results for Extraction Well Sampling 	  62
  D-2-2    Operating Conditions and Analytical Results for
          TestRun 1 (Batch)	  63
  D-2-3    Operating Conditions for Test Runs 2 through 12 (Continuous)  	  63
  D-2-4    Analytical Results for Test Runs 2 through 12 (Continuous)  	  63
  D-2-5    O&M Cost Estimates for Test Runs 2 through 12 (Continuous)  	  64
  D-3-1    Groundwater Treatment Results During the Air Stripper Study  ...  65
  D-3-2    Operating Conditions and Analytical
          Results for the Ultrox System  	  66
  D-3-3    Oxidant Cost Estimates  	  66
  D-4-1    Operating Conditions and Analytical Results  	  67
  D-4-2    Daily O&M Cost Estimates for 1,250-gpm System	  67
  D-4-3    Capital Cost Estimates for 1,250-gpm Pressurized System	  67
  D-4-4    Capital Cost Estimates for 1,250-gpm Nonpressurized System  	  67
  D-6-1    O&M Cost Estimate	  69
                                     57

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                                         Appendix D
                                        Case Studies
Introduction

This appendix summarizes several case studies on
the use of the Ultrox UV radiation/oxidation process.
These cases involve pilot-scale units as well as full-
scale operating units treating contaminated
groundwater and industrial wastewaters. No data on
VOC stripping are available from any of these case
studies. The information provided for these studies
varied widely with scant data available for some
operations and comprehensive analytical and
economic information  for others. This appendix
summarizes the following case studies:


Case
Study              Facility and Location

 D-l        Department of Energy,  Kansas City
            Plant, Missouri

 D-2        Hewlett Packard Facility, Palo Alto,
            California

 D-3        FBI Microwave, Sunnyvale, California

 D-4        Golf Course,  City of South Gate,
            California

 D-5        Xerox Facility, Webster, New York

 D-6        Koppers Industries, Denver, Colorado

 D-7        General Electric Company, Lanesboro,
            Massachusetts


Case Study D-1, Department of Energy,
Kansas City Plant,  Missouri

Introduction
This case study presents  the results of full-scale
testing of an Ultrox unit at the Allied-Signal facility
in Kansas City, Missouri.  The testing is currently
being performed under contract  by the  U.S.
Department of Energy. Over the years, the operation
of the facility has resulted in the contamination of
groundwater by total organic halogens (TOX),
including trichloroethylene (TCE). One of the
contaminated groundwater plumes, the tank farm
plume, was selected for remediation using UV
radiation, ozone, and hydrogen peroxide. Since this
process is new and information on its performance,
costs, and operating experience is not documented,
the Oak Ridge National Laboratory was requested to
evaluate the treatment process.

Testing began during 1988, and the project  is
scheduled to continue into 1990. Data from the first
year's effort are presented in a report prepared by the
Oak  Ridge  National Laboratory (Garland II, 1989).
The report discusses the mechanisms involved in the
treatment process, describes the treatment plant,
presents the testing methodology, evaluates the
results, and offers recommendations. Portions of this
appendix are taken directly from the report.


Plant Description
Based on results of bench-scale studies conducted by
Ultrox, a 725- gallon reactor, divided by baffles into 6
stages, was selected to treat the site groundwater at a
flow  rate of 25 gpm. Ozone is supplied by a generator
capable of producing 21 Ib per day at 2 percent ozone
by weight. The air dryer provides clean, dry air to the
ozone generator at 12-15 psig.

The  reactor is equipped with 72 quartz-sheathed,
low-pressure, 65-watt UV lamps located throughout
the reactor chamber. The lamps are arranged in rows
of 6, with 12 lamps in each stage. In addition,  each
stage is equipped with a sight glass and a sample
port.

Up to 50 pounds per day of hydrogen peroxide can be
supplied from either of two 55-gallon storage drums.
The  hydrogen peroxide  is mixed  with the influent
groundwater with an in-line static mixer.

Three wells are used to extract contaminated
groundwater from the tank farm plume at a rate of
approximately 6 gpm. To enhance performance  by
reducing  loads on the equipment,  one  in-line
cartridge filter is located  on the  influent line.
Following treatment, the plant effluent is discharged
into  Kansas City's municipal sewer system.
                                                58

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Methodology
The performance evaluation tests were conducted in
accordance with a  study plan that  included
monitoring the plant performance, determining the
operation and maintenance costs for the plant,
comparing the  costs with  other technologies,
evaluating contaminant removal mechanisms, and
assisting in optimization of the process. Initially, the
treatment plant was operated in a batch mode so that
all of the effluent could be contained and analyzed
prior to discharge. Four batch tests were performed to
demonstrate that the effluent criteria could be met.
The  parameters monitored  during these tests
included pH, biochemical oxygen demand, total
suspended solids, oil and grease,  13 inorganics, 34
organics, and total organic halogens.

Following the batch tests, the treatment plant was
operated in a continuous, flow-through mode with
different samples collected at  various frequencies.
The monitoring plan for the flow-through mode
showing the frequencies, parameters,  and sample
locations is shown on Table D-l-1.
Results

Batch Operations
The results of the batch operations for TOX indicate
that the influent had been adequately treated to meet
the discharge  standard  after passing the first
chamber. Most of the VOCs in the effluent were
reported at concentrations below detection limits.
The process of filtering the influent reduced all
measured VOCs to less than reportable values in
three of the four batch runs. Table D-l-2 contains the
average results from all four batch runs for a variety
of parameters that are listed in the plant's discharge
permit.


Flow-Through Operations
Although the test protocol  examined numerous
parameters, only a few of the results are presented in
this discussion. The flow data for the  treatment plant
are presented in Table D-l-3. Tables  D-l-4 and D-l-5
contain the TOX  and VOC results, respectively.
Samples were collected of the influent,  before and
after the filter, of the effluent, and at all six sample
ports. The values are monthly averages of weekly
grab samples except for the single 24- hour composite
effluent sample collected once a month for TOX.


Costs
In general,  cost data only reflect the period of time
that the plant was  treating groundwater in the flow-
through mode of operations. During  this period, the
costs  totaled approximately $8,600 for  routine
sampling and  analysis,  electricity, filters, and
Table D-1-1.  Groundwater Treatment Plant Monitoring Plan,
           Flow-Through Mode
     Frequency         Parameter3      Sample Locations'5
Continuous

Daily

Weekly












Monthly











One Time








PH
Flow
BOD
TSS
Sulfate
Sulfite
Sulfides
Nitrate
Nitrite
Ammonia
Ferrous ion
Manganous ion
TOX
VOC
TOG
Iron
Manganese
Cadmium
Chromium
Copper
Lead
Nickel
Zinc
Boron
Arsenic
Oil and grease
Total cyanide
Total plate count
Off-gas TOX
Calcium
Magnesium
Sodium
Potassium
Chloride
Fluoride
Phosphate
Carbonate
Bicarbonate
E
IBF
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E, RC
IBF, IAF, E, RC
IBF, IAF, E, RC
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
Tap
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
IBF, IAF, E
Notes:  a Parameters: BOD—biochemical oxygen demand; TSS—
       total suspended solids; TOX—total organic halogens;
       VOC—volatile  organic compounds; TOG—total organic
       carbon.
      b Sample Locations: E—effluent;  IBF—influent before filter;
       IAF—influent after filter; Tap—gas vent  from reaction
       chamber; RC—all six stages in reaction chamber.
hydrogen peroxide. An additional $65,500 was spent
during the entire testing program for sampling and
evaluation. The capital  costs for  the  bench scale
study, pilot plant study, and construction of the
treatment plant were $304,000. Considering only the
operation  and maintenance costs of $8,600 and the
total  volume of 586,000 gallons  of groundwater
treated during the 5-month flow-through mode, the
cost per volume treated is approximately $15 per
1,000 gallons.

Operations
When the plant was operating in the flow-through
mode, several shutdowns occurred.  From  May
through September the plant was shut  down nearly
50 days primarily due to excessive ozone  in the
exhaust or due to the necessity of  cleaning  or
                                                59

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Table D-1-2. Groundwater Treatment Plant, Batch Results*
Parameter
BODb
Chloride
PH
TSSb
Sulfida
Arsenic
Barium
Boron
Cadmium
Chromium
Copper
Iron
Lead
Manganese
Nickel
Zinc
Cyanide
Oil and grease
Unfiltered
Influent
(mg/L)
6
45
6.9
230
0.3
0.006
—
2.11
0.007
0.016
0.67
47.6
0.63
5.07
0.022
3.81
< 0.001
6.5

Stage 1
(mg/L)
3
—
8.3
382
<0.1
0.048
0.23
0.30
0.004
0.065
0.067
32.5
0.05
13.6
0.043
0.49
< 0.001
0.7
Effluent
Stage 6
(mg/L)
2.5
8.0
8.1
71
<0.1
0.015
—
0.19
0.009
0.047
0.12
15.3
0.042
6.8
0.023
0.34
< 0.001
0.6

Standard
(mg/L)
«
—
6-10
—
10.0
0.25
—
1.0
0.69
2.77
3.38
100
0.69
20.00
3.98
2.61
2.0
10
Notes: a These are average values for the four batch tests.
      bBOD—biochemical oxygen demand; TSS—total suspended
       solids.
Table D-1-3.  Groundwater Treatment Plant Flow Data
Month
May
June
July
August
September
Average
Flow (gal)
145,760
133,041
92,929
157,080
57,652
117,292
Flow Rate
(gpm)
5.9
5.4
5.4
7.3
10.0
6.8
Percentage of
Design Flow3
24
22
22
29
40
27
 Note:  "The design flow rate is 25 gpm.

 replacing the spargers. On the average, an operator
 at the plant spent an hour a day on monitoring and
 maintenance.
 Conclusions and Recommendations
 The effluent standards were met consistently, and
 the VOCs were eliminated in the reaction chamber.
 However,  the TOX concentrations  in  the plant
 effluent were higher than those in the sixth stage of
 the reaction chamber, and the TOX removal was not
 as high as expected.  Since the flow  rate was
 approximately 27 percent of the design  flow rate,
 while the  operating parameters varied from 50
 percent to full treatment capacity, higher removals of
 TOX were anticipated.

 A demand on the treatment chemicals was exerted by
 ammonia, ferrous ion, manganous ion, and bacteria
 as well as by the VOCs.

 A pretreatment system is an important aspect of the
 treatment plant to reduce ozone demand by removing
 scavengers and to minimize  the downtime caused by
 clogged ozone diffusers. Precipitation in the reaction
chamber, coating of the  UV lamps, and frequent
replacement of the prefilter increased the operation
and maintenance time over that expected. The plant
was out of operation 30 percent of the time, primarily
due  to excessive ozone in  the exhaust or for
maintenance and repair.

Operation and maintenance costs are much higher
than those predicted. The report  also suggests that
the economic analysis should include costs associated
with personnel maintenance and monitoring as well
as those costs incurred by regulatory compliance
monitoring.

Case Study D-2, Hewlett Packard Facility,
Palo Alto, California

Introduction
This  case  study  describes  Ultrox's   UV
radiation/oxidation project that  took place at the
Hewlett Packard facility in Palo Alto, California, in
the fall of 1988. The pilot study project was part of the
state's Department  of Health Services grant to
demonstrate the removal of toxic organic compounds
such as  benzene, toluene, xylene  (BTX),  and
ethylbenzene  from the  groundwater. Organic
compounds such as these are solvents typically used
in electronic and other manufacturing facilities.

Groundwater contamination at the Hewlett Packard
facility was discovered in 1982 and was traced to
leaking underground chemical  storage tanks. In
1988, a GAG filter system  was installed to  treat
groundwater from three wells.


Plant Description
To accommodate the existing GAC treatment system,
the Ultrox unit was installed upstream of the carbon
filters so that  the usual treatment system could
operate when the Ultrox unit, was not being tested. A
security fence was erected to protect the equipment
from tampering, and a tent was provided to shelter
the equipment from inclement weather.

Prior to treatment, groundwater was stored in a 450-
gallon tank where some volatilization could have
occurred. After the water was treated by the Ultrox
reactor, it was pumped through the GAC system and
discharged into a sewer.


Methodology
The main objective of this pilot demonstration was to
meet the same  discharge limitations as specified by
regulatory  agencies. These requirements were  to
reduce the level of total toxic organics (TTO) to less
than 1,000 ug/L with no specific  constituent greater
than 750 ug/L and to reduce the BTX, 1,1,1-TCA, and
 1,2-DCA contaminants to less than 5 ug/L.
                                                 60

-------
Table D-1-4.  Groundwater Treatment Plant Total Inorganic Halogen Results

            	        Total Inorganic Halogens (mg/L)a
                                            Reaction Chamber Stages
                                            Effluent
% Removal15
Month
May
June
July
August
September
Average
Standard
IBF<=
0.351
0.383
0.186
0.296
0.318
0.307
NAo
lAFc
0.304
0.218
0.173
0.340
0.268
0.261
NA
1
0.159
0.107
0.110
0.188
0.177
0.148
NA
2
0.087
0.064
0.100
0.141
0.145
0.107
NA
3
0.134
0.061
0.087
0.069
0.110
0.092
NA
4
0.094
0.052
0.110
0.062
0.114
0.086
NA
5
0.063
0.042
0.061
0.059
0.103
0.066
NA
6
0.067
0.028
0.051
0.053
0.095
0.059
NA
Grab
0.073
0.064
0.040
0.081
0.120
0.076
0.16
Comp.
0.090
0.085
0.048
0.147
—
0.09
0.16
Grab
76
71
77
76
55
71
NA
Comp.
70
61
72
60

66
NA
Notes:  a All samples are  weekly grab  samples (averaged monthly) except for the composite effluent sample, which  is a single  24-hour
        composite sample.
       b Percent removal values use the IAF values for initial concentrations.
       c IBF = influent before filter; IAF =  influent after filter; NA = not applicable.
Table 0-1-5. Groundwater Treatment Plant VOC Results
                                                          Volatile Organic Compounds (mg/L)a
                                                                   Reaction Chamber Stages
           Parameter
IAF»
                                                                                                             EFFb
Chloromethane
Bromomethane
Vinyl Chloride
Chloroethane
Methylene Chloride
Acetone
Carbon Disulfide
1 ,1 -Dichloroethylene
1,1-Dichloroethane
1 ,2-Dichloroethylene (Total)
Chloroform
1 ,2-Dichloroethane
2-Butanone
1,1,1 -Trichloroethane
Carbon Tetrachloride
Vinyl Acetate
Bromodichloromethane
1 ,2-Dichloropropane
cis-1 ,3-Dichloropropene
Trichloroethylene
Dibromochloromethane
1,1 ,2-Trichloroethane
Benzene
trans-1 ,3-Dichloropropene
Bromoform
4-Methyl-2-pentanone
2-Hexanone
Tetrachloroethylene
7,1 ,2,2-Tetrachloroethane
Toluene
Chlorobenzene
Ethylbenzene
Styrene
Xylene (Total)
<0.010
< 0.010
0.015
<0.010
0.021
< 0.005
< 0.005
0.014
0.019
0.714
0.007
< 0.005
< 0.005
0.014
< 0.005=
< 0.005
< 0.005
< 0.005
< 0.005
0.520
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.042
< 0.005
0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.010
< 0.010
0.010
< 0.010
0.007
< 0.005
< 0.005
0.017
0.020
0.856
0.006
< 0.005
< 0.005
0.013
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.573
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.050
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
<0.010
<0.010
0.010
<0.010
0.016
< 0.005
< 0.005
0.005
0.010
0.113
0.005
< 0.005
< 0.005
0.008
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.088
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.011
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
<0.010
<0.010
< 0.010
<0.010
0.014
< 0.005
< 0.005
0.005
0.007
0.034
0.006
< 0.005
< 0.005
0.006
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.025
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.005
0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
<0.010
< 0.010
0.010
< 0.010
< 0.005
< 0.005
< 0.005
< 0.005
0.006
0.011
0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.008
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.010
< 0.010
0.010
< 0.010
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.008
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.006
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.010
<0.010
0.010
<0.010
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
<0.010
< 0.010
0.010
< 0.010
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.010
< 0.010
0.010 v
< 0.010
< 0.005
< 0.005
< 0.005
< 0.005 ,
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005 .
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
0.005
< 0.005
< 0.005
< 0.005
< 0.005
< 0.005
Notes:  a Values are averages for all analyses performed from May through August 1988. No analyses were performed in September. All
        samples were weekly grab samples.
       b BF—influent before filter; IAF—influent after filter; EFF—effluent.
       « Carbon tetrachloride was below detectable limits in all analyses except one, in which it was at the detectable limit (0.005 mg/L).
The  results  of analytical testing on the three
extraction wells used to collect the groundwater are
shown on Table D-2-1. From this list of compounds,
                 benzene, ethylbenzene, xylene, and toluene  were
                 selected for further examination in  the pilot study
                 because they had higher concentrations than 1,2-
                                                        61

-------
Table D-2-1.  Groundwater Quality Results for Extraction Well Sampling
Sample
Location
EW-1

EW-2

Well No. 29


Combined
Influent

Date
1-19-88
1-20-88
1-21-88
2-19-88
1-19-88
1-20-88
1-21-88
2-19-88
1-19-88
1 -20-88
1-21-88
2-19-88
2-19-88d
3-22-88
4-07-88
4-19-88
5-24-88
Acetone3
34,000
27,000
28,000
43,000
28,000
15,000
19,000
62,000
ND
5,100
44,000
23,000
43,,000
61,000
35,000
51,000
36,000
1,2-DCA3
510
440
380
310
870
820
830
480
350
350
450
710
420
NDe
NDe
290
NDe
TCE3
260
ND
ND
ND
890
890
980
1,500
ND
ND
ND
ND
460
NDe
NDe,
460
NDe
Benzene3
7,800
6,900
6,100
4,400
8,100
7,900
8,000
5,800
7,400
6,900
7,800
12,000
6,100
5,000
• 4,100
3,800
. 3,200
Toluene3
1,200
1,100
830
730
1,800
1,900
1,700
1,400
7,500
7,700
8,700
11,000
. 2,800
2,000
1,900
NDe
Xylenes3
2,300
2,000
1,800
1,100
2,200
1,900
1,900
1,200
4,000
3,300
3,600
4,600
1,800
NDe
1,300
NDe
Ethyl-
benzene3
ND
ND
ND
ND
ND
ND
ND
ND
580
640
720
140
NDe
ND
NDe
TPH3
NA<=
NA
NA
NA
NA
NA
NA
NA
NA
NA
NA
NA
NA
ft | A
IMA
3,000
6,000
NA
Notes: "Concentrations reported in ppb.
      bNot detected above reporting limit.
      
-------
Table 0-2-2. Operating Conditions and Analytical Results for Test Run 1 (Batch)
Operating Conditions
Contact Time (min)
Reactor Volume (gal)
Gas Flow Rate (scfh) (Ozone 2%)
Ozone Dosage (mg/L)
Percent UV Lamps
Laboratory Analysis
Benzene (ug/L)
Toluene (pg/L)
Ethylbenzene (iig/L)
Xylene (g/L)
Total
Total Removal (%)

0
—
--
--
-

2,250
540
69.5
1,075
3,934.5
--

15
150
115
116
100

8
2
2
2
14
99.64

30
150
115
233
100

0
2
2
2
6
99.85

45
150
115
349
100

0
2
0
0
2
99.95

60
150
115
466
100

0
2
0
0
2
99.95
Table D-2-3. Operating Conditions for Test Runs 2 through 12 (Continuous)

      Test Number         2      3       4       .5       6
                               10
                                                                                               11
                                                                                                      12
Flow Rate (gpm)
Retention Time (min)
Ozone Flow Rate (scfh)
Ozone (wt %)
Ozone Dosage (rng/L)
H202 Rate (mL/min)
H2O2 Dosage (mg/L)
Total Oxidants (mg/L)
Percent UV Lamps On
5
30
90
2.16
98.29
0.00
0.00
98.29
100
5
30
45
2.16
49.14
2.00
44.39
93.53
too
5
30
68
2
68.76
0.0
0.00
68.76
100
5
30
45
0
0.00
4.00
88.77
88.77
100
5
30
45
2.16
49.14
2.00
44.39
93.53
100
5
30
45
2.15
48.92
2.00
44.39
93.30
50
5
30
40
2.05
41.46
1.70
37.73
79.19
100
7.5
« • 20
60
2.01
40.65
2.70
39.95
80.60
100
6
25 ,
50
2.04
42.98
2.14
39.58
82.55
100
4
37.5
30
2.05
38.87
1.47
40.78
79.65
100
5
30
60
2.02
61.28
2.76
61.25
122.53
100
Table O-2-4. Analytical Results for Test Runs 2 through 12 (Continuous)
Test Number
Benzene
Toluene
Ethylbenzene -
Xylene
Total
% Removed
Influent
Effluent
Influent
Effluent
Influent
Effluent
Influent
Effluent
Influent
Effluent

2
2,250
0
500
2
75
0
1,190
31
4,265
33
99.23
3
2,250
0
520
1
68
0
1,100
0
3,888
1
99.97
4
2,250
6
520
2
70
2
1,115
2
3,955
12
99.70
5
4,400
137.5
3,800
88.5
185
72.5
3,200
82.2
11,585
380.7
96.71
6
4,400
23
3,800
8.5
185
2
3,200
2
11,585
35.5
99.69
7
4,400
80
3,550
52
183.5
13.5
3,137.5
5
11,271
150.5
98.66
8
4,400
44
3,550
23
183.5
7.8
3,137.5
21.8
11,171
96.6
99.14
9
4,400
143.2
3,550
87.5
183.5
19.8
3,137.5
84.8
11,271
335.3
97.03
10
4,400
115
3,550
7.5
183.5
61
3,137.5
67
11,271
250.5
97.78
11
4,400
85
3,300
51
175
31.2
3,100
46
10,975
213.2
98.06
12
4,400
0
3,300
2
175
1
3,100
1
10,975
4
99.96
Notes: 1. Influent and effluent concentrations are reported in
      2. For the purpose of calculating, zero value was entered for the analysis of samples that were non-detectable. Also, a < 5 ug/L sample
        was approximated as 2 ug/L.
      3. On a few selected samples, duplicates were taken and therefore average values were entered.
Case Study D-3, FEI Microwave,
Sunnyvale, California
Introduction
This case study describes Ultrox's demonstration at
the FEI Microwave site in Sunnyvale, California in
the spring of 1989. The pilot study was part of the
California Hazardous Waste Reduction Program
administered by the state's Department of Health
Services grant to demonstrate the removal of
groundwater contaminants such as trichloroethylene
(TCE).
                                                    63

-------
Table D-2-5. O&M Cost Estimates for Test Runs 2 through 12 (Continuous)

 Test Number     234567
                           10
Note:  Cost estimates are reported in $/l ,000 gallons.
                                  11
                                          12
Ozone
H2O2
UV
Total
0.492
0.00
0.955
1.45
0.246
0.241
0.955
1.45
0.344
0.000
0.955
1.30
0.000
0.481
0.955
1.44
0.246
0.241
0.955
1.44
0.245
0.241
0.478
0.96
0.207
0.204
0.955
1.37
0.203
0.216
0.637
1.06
0.215
0.214
0.796
1.23
0.194
0.221
1.194
1.61
0.307
0.332
0.955
1.59
The contamination of groundwater on  the  FEI
Microwave site resulted from a leaking underground
storage  tank  holding  chemicals used  in
manufacturing   electronic    components.
Contamination of the site was discovered when FEI
acquired the property.  After a site characteristics
study, a groundwater extraction system was installed
to prevent the contaminated groundwater plume
from leaving the property. The existing groundwater
contamination and treatment system consists of nine
extraction wells of varying depth and an air stripping
unit to reduce the toxic contaminant concentrations
to the regulatory discharge limit of 0.5 ug/L for TCE
or any other toxic organic compounds.
Plant Description
The Ultrox UV radiation/oxidation system  was
installed avoiding interference with the existing air
stripping process. A fence was erected around the
equipment to prevent tampering, and a tent  was
provided to protect the equipment from the elements.

Prior to treatment, the groundwater was stored in a
6,500-gallon temporary storage tank in quantities of
no greater than required for each test (2,000 gallons).
After treatment the effluent was pumped to another
6,500-gallon tank. Following each day of testing, the
effluent was piped to the air stripper for additional
treatment prior to discharge.
Methodology
The principal goals of this pilot demonstration were
to reduce TCE below detectable limits and other
constituents to concentrations less than 5 ug/L. These
criteria were  prescribed  by the local California
Regional Water Quality Control Board for discharges
to sewers. The results of  analytical testing of the
groundwater samples from the influent and effluent
ports on the air stripper are presented in Table D-3-
l.From this list of compounds, TCE was selected for
further examination in the pilot study.  This
compound was targeted because it was  a major
contaminant in the groundwater  and because it had
been a standard component of the chemicals used for
the manufacture of electronic hardware on the site.
Thirteen tests were performed  over a two-week
period with one or two tests  run each day. The
samples were analyzed the day following  the test
runs.  All tests were conducted while the unit was
operating in a continuous mode with the.;flow rate
varying between 22 and 37 gpm.


Results

Test Operations
The operating conditions and analytical results of the
13 tests are shown on Table  D-3-2. The  influent
concentration of TCE varied from 150 to 7,750 ug/L.
The removal  efficiencies varied from 77.3 to 100
percent.

The first three test results showed that TCE was
oxidized to a nondetectable level (<5 ug/L). Tests 4,
5, 7, and 13 were run with less than all of the UV
lamps operating to assess this aspect of the
treatment.  Tests 4,  5, and 13 werie run  with 50
percent of the UV lamps operating while  varying
ozone  and hydrogen peroxide. Test 7 was conducted
without any UV lamps operating and achieved the
lowest removal of TCE (77.3 percent and 500 ug/L).
Tests  8 and 10  were run  without any ozone  to
measure the effect of different hydrogen peroxide
dosages. The higher hydrogen peroxide dosage in
Test 8 resulted in TCE concentrations in the effluent
below the detection level. Overall, 7 of the 13 test
runs achieved acceptable effluents where TCE was
less than the analytical detection limit of 5 ug/L.


Costs
The costs for oxidants were estimated for all test runs
with the Ultrox unit operating  with various oxidant
dosages. The costs per 1,000 gallons of groundwater
treated are shown in  Table D-3-3. Test 9  has the
lowest total cost for any test run  which achieved
acceptable  discharge limits. These costs do not
include costs associated with any operator who
oversees the equipment nor do they include such
items  as amortization costs of the equipment,  or
replacement of filters or spargers, or analytical
testing. The budgetary capital cost for the Ultrox UV
radiation/oxidation equipment to  treat groundwater
at this facility at 40 gpm is $120,000 (not installed).
                                                64

-------
Table D-3-1.  Groundwater Treatment Results During the Air Stripper Study
  Sample
  Location
 Date
TCEa   1,1-DCA3 1,1-DCEa 1,2-DCE3   PCE3
1,1,1-             Vinyl
TCAa   1,2-DCB3 Chloride3
                                                                                     Freona
 Methyl
Chloride3
 Total
VOCs3
 Dw.Str.   01/28/88   2,000
                  <10     <10     320       20     <10     <10      10      19     <10    2,373
02/12/88     15      <0.5     <0.5      0.7     <0.5     <0.5    <0.5    <0.5     <0.5     <0.5   ' 15.7
06/02/88      3.8     <0.5     <0.5    <0.5     <0.5     <0.5    <0.5    <0.5     <0.5     <0.5      4.3
08/30/88      3.2     <0.5     <0.5    <0.5     <0.5     <0.5    <0.5    <0.5     <0.5     <0.5      2.2
11/15/88      1.2     <0.5     <0.5    <0.5     <0.5     <0.5    <0.5    <0.5     <0.5       0.8      2.0
 Outlet
01/20/88
02/08/88
02/12/88
03/07/88
04/12/88
06/01/88
06/02/88
07/05/88
08/30/88
09/30/88
10/25/88
11/15/88
11/15/88
12/07/88
150
39
17
8.8
6.5
4.4
5.3
3.6
3.7
6.6
1.1
1.9
1.8
<0.5
<1.0
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<1.0
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
21
3.0
0.7
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<1.0
<0.5
<0.5
0.6
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<1.0
<0.5
<0.5
<0.5
<0.5
<0.8
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<1.1
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<1.0
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<1.5
<0.9
<0.5
<0.5
<0.5
0.8
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<1
<0.5
<1.0
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
<0.5
0.7
<5
<0.5
173.6
42.9
17.7
9.4
6.5
6.0
5.3
3.6
3.7
6.6
1.1
2.6
1.8
<0.5
 Inlet
01/28/88
02/08/88
03/07/88
06/02/88
08/30/88
11/15/88
5,400
4,500
4,900
6,200
11,000
3,700
<100
<50
<50
<50
<200
<50
<100
<50
<50
<50
<200
<50
210
190
170
90
<200
<50
<100
78
58
<50
<200
<50
<100
<50
<50
<50
<200
<50
<100
<50
<50
<50
<200
<50
<100
<50
<50
<50
<200
<50
<100
<50
180
260
<200
200
<100
<50
<50
150
<200
<50
5,610
4,768
5,308
6,700
11,000
3,900
 Dw.Str.   01/10/89
 Outlet    01/10/89
         01/10/89
         02/16/89
         03/14/89
2.4
<5.0
<5.0
2.5
3.8
0.5
<5.0
<5.0
0.5
0.5
<0.5
<5.0
<5.0
<0.5
<0.5
<0.5
<5.0
<5.0
<0.5
<0.5
<0.5
<5.0
<5.0
<0.5
<0.5
<0.5
<5.0
<5.0
<0.5
<0.5
--
-
--
<0.5
<0.5
<1.0
<5.0
<5.0
<0.5
<0.5
<1.0
--
-
<0.5
<0.5
<5.0
<25
<25
<0.5
<0.5
2.4
<25
<25
2.5

Inlet
01/10/89 2,900
02/16/89 2,000
<250
<250
<250
<250
<250
<250
<250
<250
<100
<250
<250
<100
<250
<250
1,200
<250
2,900
2,900
Notes: Concentrations reported in ppb.

      1,1-DCA: 1,1-dichloroethane; 1,2-DCB: 1,2-dichlorobenzene; 1,1-DCE: 1,1-dichloroethylene; 1,2-DCE: 1,2-dichloroethylene; Dw.Str.:
      down stream; PCE: tetrachloroethylene; 1,1,1-TCA: 1,1,1-trichloroethane; and TCE: trichloroethylene.
Case Study D-4, Golf Course, City of
South Gate, California

introduction
This  case   study  describes  Ultrox's   UV
radiation/oxidation project conducted at a par-3 golf
course in the City of South Gate, California, at the
end of 1987. This demonstration, supported by the
                                              California Department of Health Services, consisted
                                              of a series of tests to treat groundwater contaminated
                                              with PCE and TCA. A 675-gallon Ultrox Model P-675
                                              reactor was operated in the continuous, flow-through
                                              mode  at 50  gpm during the  test  runs. The  test
                                              program was conducted over a 6-day period to define
                                              operating, maintenance, and equipment costs for full-
                                              scale  equipment.. This is  the only case study
                                              presented in this  report with  estimated costs for
                                                     65

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Table 0-3-2.  Operating Conditions and Analytical Results for the Ultrox System
Test Number
Operating Conditions
Flow Rate (gpm)
Retention Time (min)
Gas Flow Rate (scfh)
(Ozone)
Ozone (wt %)
Ozone Dosage (mg/L)
HjO, Rate (ml/min)
H2Oj Dosage (mg/L)
TotarOxidants (mg/L)
Percent UV Lamps On
Laboratory Analysis
Inf. TCE Cone. (mg/L)
Elf. TCE Cone. (mgA.)
Removal (%)
1

37
16
150
1.97

18.3
16
48
66.3
100

6.375
ND
100
2

30
20
120
0.86

7.9
13
48
55.9
100

6.75
ND
100
3

33
18
150
2.33

24.3
14
47
71.3
100

5.75
ND
100
4

37
16
150
1.97

18.3
16
48
66.3
50

7.75
0.06
99.2
5

37
16
150
1.39

12.9
11.5
34.5
47.4
50

7.5
0.052
99.3
6

37
16
150
0.73

6.78
17
51
57.8
100

1.5
ND
100
7

37
16
150
1.57

14.6
3.3
9.9
24.5
0

2.2
0.5
77.3
8

37
16
0
0

0
16
48
48
100

1.3
ND
100
9

37
16
150
1.97

18.3
6
18
36.3
100

3.3
ND
100
10

37
16
150
0

0
8.3
25
25
100

0.15
0.02
86.7
11

37
16
150
2.94

27.3
8.3
25
52.3
100

0.229
ND
100
12 13

37 , 22
16 27
150 150
1.7 1.62

15.8 25.3
5 8.3
15 25
30.8 50.3
100 50

0.625 2.25
0.049 0.054
99.2 97.6
Note:  ND : Not detected.
Table D-3-3.  Oxldant Cost Estimates
Test Number
1
2
3
4
5
6
7
8
9
10
11
12
13
TCE Effluent Cone.
(mg/L)
ND"
ND
ND
0.06
0.052
ND
0.50-
ND
ND
0.02
ND
0.049
0.054
Ozone3
, 0.09
0.04
0.12
0.09
0.06
0.03
0.07
0.00
0.09
0.00
0.14
0.08
0.13
H202a
0.29
0.28
0.27
0.28
0.20
0.30
0.06
0.28
0.10
0.14
0.14
0.09
0.14
UVa
0.39
0.48
0.44
0.19
0.19
0.39
0.00
0.30
0.30
0.31
0.30
0.42
0.14
Total3
0.76
0.80
0.83
0.56
0.46
0.72
0.13
0.58
0.50
0.45
0.58
0.58
0.41
Note:  a Cost estimates reported in $/1,000 gallons
      b ND: Not detected.

pressurized and nonpressurized systems. Twelve
tests were run in which the oxidant doses were varied
while attempting to achieve  the desired  treatment
standard  of 2 ug/L for  PCE. The untreated
concentration of TCA, ranging from nondetectable to
3 ug/L, was less than the level of concern.

Results

Operations
A description of the operating conditions and the
analytical  results are presented in Table D-4-1. As
shown, the influent water PCE concentrations varied
between 14 and 18 ppb with the average being 17
ppb. Six tests (Nos. 2, 3, 5, 7, 9, and 11) produced
water with a PCE concentration of less than 2 ppb,
which was the desired treatment standard.

TCA was also detected in the water at concentrations
of nondetectable to 3 ppb,  which is below present
drinking water standards. The various operating
conditions did not significantly reduce the TCA with
the exception of Test No. 9,  which used UV-hydrogen
peroxide.
Costs
The projected O&M costs per day for a continuously
operating system at 1,250 gpm for the successful test
runs are presented on Table D-4-2. Test No. 11, run
without UV or hydrogen peroxide, shows the lowest
O&M costs. Tables D-4-3 and D-4-4 present capital
costs estimated  for pressurized (80  psig)  and
nonpressurized systems. The lowest capital costs for
both systems are those  associated with Test No. 11.
Test No. 7 had the next least expensive capital costs.

Case Study D-5 Xerox Facility, Webster,
New York

Introduction
This  case  study describes  Ultrox's  UV
radiation/oxidation testing of an approximately one-
quarter scale unit on contaminated groundwater at
the  Xerox Corporation,  Salt Road  site.  The
contaminants include TCE and vinyl chloride with
total volatile organics ranging in concentrations from
1 to 10 mg/L. The information contained in this
appendix is based on a draft, interim report by Xerox
                                                 66

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Table D-4-1. Operating Conditions and Analytical Results

Test No.
1
2
3
4
5
6
7
8
g
10
11
12

Ozone Dosage
Med.
High
High
0
0
0
Med.
0
0
Low
Med.
Low

H2O2 Dosage
0
0
Med.
High
Med.
0
Med.
Med.
Med.
Low
0
0
Operating UV
Lamps
All
All
0
0
1/3
All
0
1/4
1/2
0
0
0
PCE
Influent
14
20
17
17
17
17.5
18
16
16
18
—
18
Effluent
4
0.2
0.4
14
0.1
4
0.2
13
1.3
2.2
0.32
4.4
TCA
Influent
3
ND
ND
ND
ND
0.4
0.5
1.3
1.2
ND
ND
ND
Effluent
2.4
ND
ND
ND
ND
0.5
0.4
1.3
0.3
ND
ND
ND
Note:   1. All tests run at 50 gpm.
        2. ND: Not detected.
        3. Concentrations reported in ppb.
Table 0-4-2.  Daily O&M Cost Estimates for 1,250-gpm System
Test No.
2
3,
5
7
9
11
Ozone
164
164
0
110
0
110
H2O2
0
54
54
51
54
0
UV Power
235
0
78
0
118
0
UV Maint.
80
0
27
0
40
0
Total
479
218
159
161
212
110
Note:  1. All values reported in dollars.
       2. Assumes cost of electrical energy is at $0.085/kWh.
       3. An additional $21/day O&M costs is required for 80-psig pressurized systems.
Table D-4-3.  Capital Cost Estimates for 1,250-gpm Pressurized System

         Test No.              Ozone Generator            H2O2 Supply
Reactor
Total
2 162,000
3 162,000
5 0
7 125,000
9 0
11 125,000
0
10,000
10,000
10,000
10,500
0
400,000
85,000
300,000
85,000
350,000
85,000
562,000
257,000
310,000
220,000
360,000
210,000
Note:   All values reported in dollars.
Table D-4-4.  Capital Cost Estimates for 1,250-gpm Nonpressurlzed System
Test No.
2
3
5
7
9
11
Ozone Generator
122,000
122,000
0
100,000
0
100,000
H2O2 Supply
0
10,000
10,000
10,000
10,000
0
Reactor
360,000
50,000
260,000
50,000
315,000
50,000
Total
482,000
182,000
270,000
160,000
325,000
150,000
Note:   All values reported in dollars.
                                                            67

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and personal communication. No cost data were
provided.


Plant Description
A 650-gallon Ultrox reactor was installed at the site
in March 1989 for a series of pilot tests. Recovery well
pumps provide the hydraulic pressure necessary for
process flows.  A 5-micron  fiber bag filters the
groundwater prior to treatment. During the pilot
tests, effluent from the Ultrox system was sent to a
storage tank and subsequently pumped to an air
stripper  to  guarantee  effluent  discharge
requirements. The effluent, currently discharged to a
sanitary sewer, will later be sent to a surface stream
from the air stripper during full-scale operation.


Methodology
During the test period, the groundwater flow  rate
varied from 30 to 50 gpm, with an additional 10 gpm
acting as  cooling water for the air compressor and
ozone generator. A 50 percent solution of hydrogen
peroxide was added to the influent at a dose of 30
mg/L. The ozone dosage was set at 58 mg/L  with a
constant pressure of 15 psig. The feed mixture was
calibrated to deliver 2 percent ozone in the reactor.
All 72 U V lamps were operating during the test runs.


Twenty-four sampling events were conducted during
the test period, with daily samples collected during
the first week of operation and twice weekly
thereafter. Influent was sampled prior  to the
hydrogen peroxide injection; effluent was sampled
from the sixth cell sampling port of the reactor.
 Results

 Analytical
 For the test runs, the  average  contaminant
 concentration for total volatile organics was 3,048
 ug/L. The removal efficiency  averaged 93 percent
 with 3  constituents  below  90 percent  and 21
 compounds  above  90 percent. The  removal
 efficiencies for specific compounds were as follows:
   Compound

   Vinyl Chloride
   Toluene
   Tetrachloroethylene
   1,2-Dichloroethylene
   Trichloroethylene
   1,1,1-Trichloroethane
   1,1-Dichloroethane
Removal Efficiency (%)

        100
        100
        100
         98.6
         92.2
         36
          0.0
                         Maintenance
                         Daily inspection during the test period revealed that
                         periodic adjustments are required to maintain peak
                         operating efficiency. The groundwater at the site
                         contains relatively high concentrations of iron which
                         affected the UV  lamps.  Based  on the  tests,
                         inspections would be prudent to replace lamps and
                         clean the quartz sleeves. Additional  maintenance
                         would be  required to check  and  change the
                         compressor oil  and filter  as well  as inspect and
                         change the ozone decomposer catalyst.

                         Case  Study D-6 /Coppers Industries,
                         Denver, Colorado

                         Introduction
                         This case study briefly presents treatment results of
                         an Ultrox system employed by Koppers Industries,
                         Inc., on wastewater from a wood processing facility.
                         An Ultrox unit, operating since December 1985 with
                         UV  and ozone, is used  to treat  the organic
                         contaminants, phenol and pentachlorophenol (PCP),
                         from the plant's wastewater. A pretreatment system
                         consists of  pH adjustment, oil removal, and
                         flocculation and settling of heavy metals.

                         The organic concentrations of the influent typically
                         range between  150 to  200  mg/L for phenol and are
                         about 1 mg/L for PCP. Oil and grease are measured at
                         about 3 percent in the raw wastewater.
                          Results

                          Analytical
                          The results of effluent testing from several months of
                          operation based on 1-day composites are presented as
                          follows:
                                             5/88
8/88   11/88   3/89
7.2 7.0
0.18 0.5
145.0 65.0
15.0 78.0
11.6 12.2
0.44 0.15
38.0 45.0
<1.0 24.0
Constituent

pH
PCP (mg/L)
Phenol (mg/L)
Oil (mg/L)

The flows in March 1989 were reported to be 5,211
gpd on an average daily basis, with a maximum daily
How of 16,047 gpd.


Costs
The operating and maintenance costs per  1,000
gallons of treated wastewater for the entire system
are presented in Table D-6-1. The capital cost of the
                                                 68

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Table D-6-1. O&M Cost Estimate
Item
Flocculating agents
Sulfuric acid
Caustic soda
Defoamer
Electricity
Labor
Analysis
Effluent disposal
$/l,OOOgal
5.79
.39
.81
.42
2.11
1.40
1.83
4.64
 Total
$17.39/1,000 gal
principal VOCs and  PCBs to  levels below the
analytical detection  limits. Both oxidants, in
conjunction with UV radiation, achieved  VOC
reductions greater than 99.9 percent. These tests also
indicated that hydrogen peroxide alone could achieve
substantial VOC and PCB removals. Trans-1,2-
dichloroethylene, the VOC with the highest influent
concentration, was more difficult to treat than vinyl
chloride.  Another VOC, 1,1,2-TCA,  present in low
concentrations in the influent, appeared to be
resistant to oxidation, or a product of degradation.
entire treatment system installed was $550,000, of
which  $200,000  was for  the  Ultrox  UV
radiation/oxidation portion.

Case Study D-7 General Electric
Company, Lanesboro, Massachusetts

Introduction
This case study describes the Ultrox technology's
performance in a treatability study that took place at
General Electric Company's Rose Site, Lanesboro,
Massachusetts  in the fall of 1987. In addition to UV
radiation/oxidation, the project evaluated the
effective use of air stripping and carbon adsorption in
treating groundwater contaminated with several
volatile compounds including vinyl chloride and
trans-l,2-dichloroethylene, and trace concentrations
of PCBs.
                                                  References
                     Case
                     Study

                      1.
                      2.
       Garland II, S.B., 1989. Annual Report, An
       Evaluation of the Use of a Combination of
       Ozone, Ultraviolet Radiation, and Hydrogen
       Peroxide   to   Remove  Chlorinated
       Hydrocarbons from Groundwater at the
       Department of Energy Kansas City Plant,
       Oak Ridge National Laboratory Report,
       ORNL/TM-11056.
       Ultrox   International,   1989.   The
       Demonstration of the Ultrox UV/Oxidation
       Treatment of Contaminated Groundwater at
       the Hewlett Packard Facility, Palo Alto,
       California.
Plant Description
An Ultrox Model P-75 pilot system, with a wet
volume of 75 gallons, 6 cells, and 30 UV lamps, was
used in the  study.  The unit was supplied with
groundwater from a single well that passed through a
10-micron cartridge filter prior to treatment.


Methodology
Tests were performed on the Ultrox  system  to
evaluate the use of UV-ozone and UV-hydrogen
peroxide. All  UV lamps remained operating while
the hydraulic retention times and oxidant dosages
were varied. UV-ozone test conditions had flow rates
between 1.5 and 2 gpm with ozone dosages between
160 and 600 mg/L at concentrations of approximately
3 percent. UV-hydrogen peroxide test conditions had
flow rates between 0.75 and 1 gpm with hydrogen
peroxide  dosages between 53 and  580  mg/L. Batch
tests preceded continuous-flow operations for each
phase of study.


Results
Both treatment  combinations, UV-ozone and UV-
hydrogen peroxide,  were able  to reduce the two
                      3.     Ultrox International, 1989. Report on the
                            Demonstration of the  UV/Oxidation
                            Treatment  of  Groundwater  at  FBI
                            Microwave, Sunnyvale, California.


                      4.     Ultrox International, 1988. Ultrox Pilot
                            Plant Treatment Demonstration Report for
                            the City of South Gate, California.


                      5.     Xerox Corporation, 1989. Draft Interim
                            Report, Ultrox Performance Summary and
                            personal communication between Dr. Robert
                            Heeks, Xerox Corporation, and Dr. Gary
                            Welshans, PRC.


                      6.     Koppers  Industries,  1989. Personal
                            communication between Mr. Marvin Miller,
                            P.E.,  Koppers Industries, and Dr. Gary
                            Welshans, PRC.


                      7.     Blasland  & Bouck Engineers, P.C., 1988.
                            Draft Report, Ground-Water Treatability
                            Report,   Rose    Site,    Lanesboro,
                            Massachusetts.
                                               69
                                                                  •frU.S. GOVERNMENT PRINTING OFFICE: 1990-751-429

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