AEPA
                                 United States
                                 Environmental Protection
                                 Agency
                                   EPA/540/F-92/004
                                   February 1992
                                 SUPERFUND INNOVATIVE
                                 TECHNOLOGY EVALUATION
                            Emerging Technology Bulletin

                   Laser Induced Photochemical Oxidative Destruction

                       Energy and Environmental Engineering, Incorporated
Technology Description:  The process developed by Energy
and Environmental  Engineering,  Incorporated,  is designed to
photochemically oxidize  organic  compounds  in wastewater by
applying ultraviolet radiation using an Excimer laser. The photo-
chemical reactor can destroy  low to moderate concentrations of
organics in water. The energy is sufficient to fragment the bonds
of organic compounds, and the radiation is not absorbed to any
significant extent by the water molecules in the solution.  The
process is envisioned as a final treatment step to reduce organic
contamination in ground water and industrial wastewaters to
acceptable limits.

The overall reaction chemistry uses hydrogen peroxide as the
oxidant in the reaction:

    CaHbX + (2a+0.5 (b-1))H2O2"»-» aCO2 + (2a+(b-1 ))H2O + HX

where C HbX is  a halogenated toxic component in the aqueous
phase, the reaction products  are carbon dioxide, water, and the
corresponding halogen acid, HX.
                    The existing process equipment has a capacity of 1 GPM when
                    treating a solution containing 32 ppm of total organic carbon. It
                    consists of a photochemical reactor, where oxidation is initiated,
                    and an effluent storage tank to contain reaction products (Figure


                    The skid-mounted system can be used in the field and stationed
                    at a site. The exact makeup of the process will  depend on the
                    chemical composition of the groundwater or wastewater being
                    treated.

                    Typically, contaminated groundwater is pumped from a feed well
                    through a filter unit to remove suspended particles. The filtrate is
                    then fed to the photochemical reactor and irradiated. The chemi-
                    cal oxidant (H2O2) is introduced to the solution to provide hydroxyl
                    radicals required! for oxidation.

                    The roactor effluent is directed to a vented storage tank, where
                    the CO2 oxidation product is vented.  An appropriate base (such
          Waste
          Water
                                Q
FC
                               Metering Pump
                                                       Initiation
                 Photochemical
                    Reactor
                                                                         Vent
               Decontaminated
                  Effluent
                                                                             Effluent
                                                                           Storage Tank
                                                                           & Propagation
                                                                             Reactor
Figure 1.  Process Flow Scheme,
                                                                                    Printed on Recycled Paper

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as CaCO,) may be added to the storage tank to neutralize any
hatogenafed acids formed when treating fluids contaminated with
halogenated hydrocarbons.

The reaction kinetics depend on:

        a)  toxicant concentration
        b)  peroxide concentration
        c)  irradiation dose
        d)  irradiation frequency
Waste Applicability:  This technology can  be applied  to
groundwater and industrial wastewater containing organics.
T©St Results: Table 1 presents typical reaction times for given
levels of destruction for several toxicants of concern.
7aWe "t . Destftsstlen of Toxic Organics by Laser-Induced Photochemical
Oxidation
Reaction Time (hr) Destruction Achieved
Benzene
B@ftZidin8
Ghhfobmzena
Chfofophenol
Dieftlofoethene
Phmoi
96
268
114
72
624
72
0.91
0.88
0.98
0.99
0.88
0.99
Destruction Achieved,,,,-^,
.,„
Where
C^ * » Contaminant Concentration in to reactor, with irradiation
C^" = Contaminant Concentration out of reactor, with irradiation
Cfe   «• Contaminant Concentration in to reactor, no irradiation
O   = Contaminant Concentration out of reactor, no irradiation
                   Table 2 lists the compounds that can be treated successfully by
                   Laser-Induced Photochemical Oxidative Destruction.
                   Table 2. Compounds Treated with UV/Oxidation
Ethers
BTEX
Phenol
TCE
PCE
DCE
Polynitrophenols
Ketones
Vinyl Chloride
Pesticides
Citric Acid
TCA
DCA
Ma a,
Cresols
PCBs
PCP
TNT
Aromatic Amines
Complexed Cyanides
PolynuclearAromatics
Dioxins
Hydrazine
RDX
1,4 Dioxane
EDTA
Hydrazine
                   The process is now entering the initial phases of commercializa-
                   tion, with the company offering to conduct treatability studies for
                   prospective clients.  Preliminary cost evaluation shows that the
                   process is very competitive compared  to  other UV oxidation
                   processes and carbon adsorption.
                   For Further Information:

                   EPA Project Manager:
                   Ronald F. Lewis
                   U.S. EPA Risk Reduction Engineering Laboratory
                   26 West Martin Luther King Drive
                   Cincinnati, OH 45268
                   (513) 569-7856 (FTS: 684-7856)
                   Technology Developer Contact:

                   James H. Porter
                   President
                   Energy and Environmental Engineering, Inc.
                   East Cambridge, MA 02141
                   617-666-5500
United States
Environmental Protection
Agency
Center for Environmental
Research Information
Cincinnati, OH 45268
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EPA/540/F-92/004

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