Abstract: A single step wet oxidation process for treating wastewaters containing organic species, with or without heteroatoms, and anions of strong acids, e.g. sulfate or phosphate ion, or cations of strong bases, e.g., sodium, potassium or calcium ions, and which may contain ammonium ion and/or nitrate ion in addition to added ammonium ion and/or nitrate ion was developed which on thermal treatment near the critical temperature of water removes substantially all the COD and nitrogen through conversion to water, carbon dioxide or carbonate species, nitrogen gas and small amounts of nitrous oxide. Key to the success of the process is the balancing of all reducing species with an equivalent amount of oxidizing species and the balancing of all strong acid anions with strong base cations and including at least 0.06 acetate ion for moles of nitrate in the wet oxidation process.

Abstract: Wastewater from the aldolization reaction is purified by adjusting its pH to 0 to 6, followed by extraction with monohydric alcohols having at least 8 carbon atoms, hydrocarbons having at least 6 carbon atoms, and mixtures thereof. In some cases, adjustment of the pH causes the formation of an organic phase, which is separated from the remaining wastewater before extraction.

Abstract: A process for the treatment of waste waters containing chemically reducible dissolved organic and inorganic pollutants and suspended mater in particulate or colloidal form. The process comprises of contacting the water with metallic iron or ferrous ions (Fe2+), or mixtures thereof, in the presence of promoter metals, such as Cu, Pd, Pt, Au, Ag, and Ni, or oxides, sulfides and other insoluble compounds of these meals, which catalyze the redox reductions carried out by the iron or ferrous reagents. The production of ferric ions (Fe3+) as a final iron oxidation product allows for the simultaneous coagulation and precipitation of suspended colloidal and particulate solids out of the aqueous phase. In addition to the main reductive reaction scheme, the system performs a multitude of secondary reactions involving the ferrous and ferric ions produced in-situ which allows for the simultaneous removal of specific target pollutants, such as phosphate and hydrogen sulfide.

Abstract: A sparging system and process for in-situ removal of contaminants from soil and an associated subsurface groundwater aquifer of a site is disclosed. The sparge system is capable of extracting contaminant in the form of gas from groundwater in a gas/gas/water reaction. The system includes at least one microporous diffuser having a porosity matched to a soil porosity. The microdiffuser is in an injection well. Ozone or other oxidizing gas in the form of bubbles is injected into the site to extract volatile dissolved contaminants for in-situ decomposition. A pump and a pneumatic packer are disposed to alternate pumping and bubble injection into the well to maximize dispersal of bubbles within and outward from the well casing, and to provide uniform dispersion of the bubbles as they travel through the site formation.

Abstract: A process for reducing the loading of wastewaters produced in the preparation of hydroxyl and carbonyl compounds from hydroperoxides by the Hock process, which may be acidic, by treating the wastewaters with an oxygen-containing gas at a pressure greater than 25 bar absolute and at a temperature of 150-250° C. Surprisingly, improved degradation rates are achieved under these conditions.

Abstract: A method and apparatus are disclosed in which alkanes such as butane are used to degrade pollutants such as tetrachloroethylene (PCE) and carbon tetrachloride (CT) at contaminated sites. In a preferred embodiment, pollutant concentrations are reduced by injecting a butane substrate into a contaminated area to stimulate the growth of anaerobic butane-utilizing bacteria which degrade the pollutants. In addition to the anaerobic treatment, the area may optionally be treated aerobically by switching from anaerobic to aerobic conditions.

Abstract: Groundwater, or other water contaminated with chlorinated organic contaminants, is passed through a permeable body of iron particles. The particles are coated with nickel, but the coating is incomplete, in that, in patches, the iron is directly exposed. The contaminants break down under prolonged proximity to the iron, the nickel enhancing the catalytic effect. The rate of breakdown is much faster than when bare iron particles were used. When the nickel is alloyed with phosphorus, or boron, even more rapid breakdown rates are achieved.

Abstract: The present invention relates to a method of treating alkaline waste water originating from washing spent oil which has undergone an alkaline treatment with water and which contains organic material. This method can produce water which can be discharged into conventional industrial water treatment facilities or which can be used directly as a base for preparing fertilizers or for preparing an agent for preventing ice formation on road surfaces.

Abstract: A method and apparatus is disclosed for oxidation of aqueous mixtures of organic material, including toxic material in the presence of inorganic materials, by reaction of said material with water and oxygen at supercritical conditions. Oxygen and the aqueous mixture are separately pressurized to greater than about 218 atmospheres, combined to form a reaction mixture and then directed through a tubular reactor having a substantially constant internal diameter. The velocity of the reaction mixture is sufficient to prevent settling of a substantial portion of solids initially present in the reaction mixture and of solids which form during passage through the reactor. The mixture is heated to temperature above about 374° C. in the tubular reactor. A substantial portion of the organic material in the reaction mixture is oxidized in the tubular reactor to thereby form an effluent mixture.

Abstract: A process for breaking down aromatics in industrial wastewaters that contain small amounts of aromatics by reaction with an ozone-containing oxygen stream at a temperature of from 40 to 70° C. and at a pH of from 4 to 7, involves treating industrial wastewaters that contain small amounts of aromatics in two stages with an oxygen stream that contains from 5 to 8% by volume of ozone with thorough mixing by causing the wastewater to flow upward through two reaction zones, the overflow of the wastewater at the top of the first reaction zone entering the second reaction zone at the base, the purified wastewater being obtained at the top of the second reaction zone, the ozone-containing oxygen stream first entering at the base of the second reaction zone, and the waste gas obtained at the top of the second reactor being introduced at the base of the first reaction zone, and, furthermore, a gas containing less than 0.2% by volume of ozone being obtained at the top of the first reaction zone.

Abstract: The invention concerns a method for treating an aqueous solution derived from sluicing of crude mononitrated or dinitrated aromatic compounds obtained by nitration of the corresponding aromatic compounds, consisting in: (a) contacting said aqueous solution with said aromatic compound thereby obtaining an aqueous phase and an organic phase; (b) recycling said organic phase in the nitration process; (c) distilling said aqueous phase; (d) recycling the resulting concentrated acid solution in the nitration process; (e) recycling or eliminating the recuperated water after distillation.

Abstract: A system and method are disclosed in which butane-utilizing bacteria are used to degrade pollutants such as trichloroethene (TCE) and trichloroethane (TCA) in-situ at contaminated sites. In a preferred embodiment, pollutant concentrations are reduced by injecting a butane substrate and an oxygen-containing gas into a contaminated area to stimulate the growth of butane-utilizing bacteria which degrade the pollutants by cometabolism or direct metabolism. Use of the butane/oxygen injection system results in substantially improved treatment of contaminated sites.

Abstract: Aromatic nitro compounds in waste waters from nitrobenzene production plants are degraded by treatment with ozone at 60-100° C. 1.5-10 bar and pH 3 to 12.

Abstract: A process for upgrading aqueous acrylonitrile waste streams containing organic material comprising atomizing an acrylonitrile waste water stream containing organic material, introducing the atomized acrylonitrile waste water stream at a temperature below the decomposition temperature of the organics present in the waste water stream, into a reaction zone containing a catalyst and at least one reactant gas, reacting the atomized waste water stream and reactant gas in the presence of the catalyst to convert at least some of the organics in the waste water stream into at least one compound selected from the group consisting of acetonitrile, hydrogen cyanide and acrylonitrile.

Abstract: A method for separating benzene from a hydrocarbon mixture containing benzene and at least one other organic material is carried out by treating the hydrocarbon mixture with at least one cyclodextrin to form complexes of the cyclodextrin with at least a portion of the benzene present in the hydrocarbon mixture. The cyclodextrin-benzene complexes then are separated from the hydrocarbon mixture.

Abstract: A process and catalyst for the conversion of contaminants in an oxygen containing contaminated stream comprises passing the oxygen containing contaminated stream over a photocatalyst comprising titanium, zirconium and silica while irradiating the foregoing catalyst with ultraviolet light.

Abstract: Butane-utilizing bacteria are used to degrade hydrocarbon pollutants such as trichloroethene (TCE). In-situ or ex-situ techniques may be used to reduce or eliminate hydrocarbon pollutants from liquid, gas and solid sources. In a preferred embodiment, TCE concentrations in various aqueous environments are reduced by contacting a contaminated water source with butane-utilizing bacteria in the presence of oxygen to degrade the TCE by cometabolism or direct metabolism. Suitable butane-utilizing bacteria include Pseudomonas, Variovorax, Nocardia, Chryseobacterium, Comamonas, Acidovorax, Rhodococcus, Aureobacterium, Micrococcus, Aeromonas, Stenotrophomonas, Sphingobacterium, Shewanella, Phyllobacterium, Clavibacter, Alcaligenes, Gordona, Corynebacterium and Cytophaga. The butane-utilizing bacteria have relatively low TCE toxicity in comparison with conventional methane-utilizing bacteria, and demonstrate an improved ability to degrade TCE.

Abstract: The present invention relates to a method of using a protein-polysaccharide complex composition as an adsorbent and filtering aid for in the processing of fluids or solids to absorb or decompose a variety of separable components including halogenated organic compounds such as PCBs and dioxins.

Abstract: A method has been discovered for removing organics, such as water soluble organics (WSO), from fluids containing water, such as oil process water, by contacting the fluid with an effective amount of an organic ammonium salt. No added acid is necessary, although in some embodiments, weak acids such as glycolic acid, can be used to give synergistic improvement in organic removal. Suitable organic ammonium salts have the formula:R.sup.1 R.sup.2 R.sup.3 N.sup.+ H X.sup.-where R.sup.1 is a saturated or unsaturated alkyl group or an aryl group, or saturated or unsaturated alkyl group or an aryl group substituted with a heteroatom selected from the group consisting of N, O, S, P and halogen; R.sup.2, and R.sup.3 are independently H or a saturated or unsaturated alkyl group or an aryl group, or saturated or unsaturated alkyl group or an aryl group substituted with a heteroatom selected from the group consisting of N, O, S, P and halogen; and X is a halogen atom or an anion of a protic acid.

Abstract: Soluble ferric chelates and peroxide are employed in a method for degrading organic contaminants such as pesticides in soil. In the practice of the method, soil containing an organic compound having at least one oxidizable aliphatic or aromatic functional group is contacted with an active ferric chelate and a peroxide such as hydrogen peroxide in amounts effective to achieve degradation of the compound in the presence of water at the pH of the soil. In preferred embodiments, at least about 3%, and in some cases at least about 5% or 10%, of the ferric chelate does not sorb to the soil. Example ferric chelates include ferric nitrilotriacetate, ferric hydroxyethyleniminodiacetate, ferric gallate, and mixtures thereof; ferric nitrilotriacetate and ferric hydroxyethyleniminodiacetate are especially preferred in some embodiments.

Abstract: Butane-utilizing bacteria are used to degrade pollutants comprising polychlorinated biphenyls (PCBs). In-situ or ex-situ techniques may be used to reduce or eliminate PCB pollutants from liquid, gas and solid sources. In a preferred embodiment, PCB concentrations in various aqueous environments are reduced by contacting a contaminated water source with butane-utilizing bacteria in the presence of oxygen to degrade the PCB by cometabolism or direct metabolism. Suitable butane-utilizing bacteria include Pseudomonas, Variovorax, Nocardia, Chryseobacterium, Comamonas, Acidovorax, Rhodococcus, Aureobacterium, Micrococcus, Aeromonas, Stenotrophomonas, Sphingobacterium, Shewanella, Phyllobacterium, Clavibacter, Alcaligenes, Gordona, Corynebacterium and Cytophaga.

Abstract: According to this method for the adsorptive extraction of hydrocarbons from aqueous solutions of hydrocyanic acid, the initial solutions containing 1 to 50 wt. % hydrocyanic acid and 2 to 1000 wt. ppm aliphatic and/or aromatic hydrocarbons, the latter having 6 to 30 C atoms each, are passed, preferably continuously, at temperatures between 2 and 50.degree. C. and at a maximum flow velocity of 500 m/h through a fixed-bed, activated-carbon adsorber whose interior surface is preferably>100 m.sup.2 /kg. In this way it is possible to quantitatively free aqueous solutions of hydrocyanic acid from hydrocarbons, in particular from benzene, with means of relatively low technical complexity.

Abstract: Enhanced synthesis of transition metal dithiolene complexes is described. [1,2-bis(Trifluoromethyl)ethylene-1,2-dithiolato]nickel selectively and reversibly binds olefins (C.sub.2 to C.sub.6). Under the same conditions, the complex does not react with H.sub.2 O, C.sub.2 H.sub.2, CO, and H.sub.2, and only slowly reacts with H.sub.2 S at high concentrations. The compositions are useful for selective removal and recovery of olefins from process streams containing contaminants such as CO and H.sub.2 S.

Abstract: Alkane-utilizing bacteria are used to degrade pollutants comprising petroleum compounds. In-situ or ex-situ techniques may be used to reduce or eliminate petroleum pollutants from liquid, gas and solid sources. In a preferred embodiment, petroleum concentrations in various environments are reduced by contacting the petroleum pollutants with butane-utilizing bacteria in the presence of oxygen to degrade the petroleum pollutants by cometabolism or direct metabolism. Suitable alkane-utilizing bacteria include Pseudomonas, Variovorax, Nocardia, Chryseobacterium, Comamonas, Acidovorax, Rhodococcus, Aureobacterium, Micrococcus, Aeromonas, Stenotrophomonas, Sphingobacterium, Shewanella, Phyllobacterium, Clavibacter, Alcaligenes, Gordona, Corynebacterium and Cytophaga.

Abstract: A system and method for providing an oxidized liquid effluent stream substantially free of volatile compounds is provided. The system includes a stripper positioned downstream of a separator, or disposed within a separator. The method involves volatilizing volatile compounds by performing a separation followed by stripping, or in the same chamber as the separation. In another aspect, the invention involves adjusting the pH of the oxidized waste stream prior to stripping in order to convert ionic species to volatile species that can be removed by stripping.

Abstract: A process for removing toxins from blood is disclosed. The process involves contacting the blood with a microporous ion exchanger to remove toxins in the blood. Alternatively, the blood can be contacted with a dialysis solution which is then contacted with the ion exchanger. The microporous ion exchangers are represented by the following empirical formulae:A.sub.p M.sub.x Zr.sub.1-x Si.sub.n Ge.sub.y O.sub.m (I)andA.sub.p M.sub.x Ti.sub.1-x Si.sub.n Ge.sub.y O.sub.

Abstract: An apparatus and method for removing hydrocarbon contaminants and heavy metal ion contaminants from wastewater stream comprising the introduction of iron ions into the stream. In one embodiment, the ions are introduced by applying an electrical current through a bed of iron particulates in the form of steel wool and iron nodules. In another embodiment, the iron salts are added to the waste stream and the iron ions are reduced to a more reactive lower valence state by electric current.

Abstract: Arsenic and TOC are removed from drinking water or wastewaters by use of finely-divided metallic iron in the presence of powdered elemental sulfur or other sulfur compounds such as manganese sulfide, followed by an oxidation step. A premix may be produced for this process, by adding the iron, sulfur and oxidizing agent to water in a predetermined pH range. The iron and sulfur are mixed for a period of time dependent upon the temperature and pH of the water and the presence of complexing or sequestering minerals and organic acids in the water. An oxidizing agent is added to the mixture and agitating is continued. In a preferred embodiment the oxidizing agent is hydrogen peroxide. Water is decanted from the mixture after a sufficient reaction time, to produce a concentrated premix. This premix can be added to water intended for drinking or to industrial effluents containing toxic materials.

Abstract: A process is disclosed which comprises the steps of: slurrying sludge to be treated; applying ultrasonic radiation to the slurry to decompose dioxins contained in the sludge in a reaction field developed by the application of the ultrasonic radiation and to transfer pollutants including the resulting decomposition products from a solid phase to a liquid phase of the slurry; and separating the slurry into the liquid phase containing the pollutants and the solid phase free from dioxins by solid-liquid separation means.

Abstract: A method of forming reactive oxygen species by solubilizing a metal ion from a metal oxy(hydr)oxide compound with an iron oxy(hydr)oxide solubilizing chelator to yield a first soluble metal ion chelate complex. The metal ion is transferred from the chelate complex to a free redox cycling chelator to form a second metal ion chelate complex which reduces the metal ion to a reduced metal species. The reduced metal species is reacted with an oxygen containing oxidant to yield a free redox cycling chelator and a reactive oxygen species. The reactive oxygen species may be used to oxidize a target substrate. The preferred metal ion is a cationic transition metal, such as iron or manganese. A preferred iron oxy(hydr)oxide solubilizing chelator is oxalic acid. The method is generally performed at acidic pH.

Abstract: This invention relates to a process for the purification of waste waters containing organic and, should the situation arise, inorganic sulphur compounds, which waste waters contain a proportion of mercaptobenzothiazole and/or derivatives thereof and, should the situation arise, a proportion of benzothiazole and/or derivatives thereof and/or mercaptobenzimidazole and/or derivatives thereof and, should the situation arise, thiosulphate, whereby the waste waters are treated with an extracting agent comprising salts of aliphatic amines and aliphatic and/or aromatic hydrocarbons.

Abstract: A process for hot or supercritical water oxidative decomposition of wastes, particularly halogenated organic compounds, is described. The process employs a heterogeneous reagent which accelerates the decomposition and is effective to neutralize acidic byproducts. The reagent is maintained in suspension throughout the reaction by operating at conditions of temperature and pressure at which the heterogeneous reagent is largely or fully insoluble in water, and preferably at which liquid water is not present. Production of potentially corrosive brine is also minimized by operating at conditions under which sodium chloride is insoluble.

Abstract: There are here provided a method for biodegrading trichloroethylene which comprises the step of bringing an aqueous medium containing trichloroethylene into contact with microorganisms having a trichloroethylene degrading ability derived from intestines of termites to degrade trichloroethylene; a method for obtaining the microorganisms; a method for remediating a soil by the use of the microorganisms; and a method for biodegrading an chlorinated organic compound with the microorganisms.

Abstract: A method and apparatus is provides for decontamination of soil from contaminates such as polychlorinated biphenyls. The method involves (a) admixing a short chain alcohol and a ethoxylated alcohol to provide a solvent composition, (b) admixing the solvent composition with the contaminated soil to extract the contaminant from the soil into the solvent to form contaminated solvent, (c) separating the soil from the contaminated solvent, (d) washing of the decontaminated soil with water to remove residual solvent from the soil, and (e) distillation of the contaminated solvent to separate the reusable short chain alcohol as a light fraction from a heavy fraction containing the ethoxylated alcohol and the contaminant.

Abstract: Methods and compositions are disclosed for the microbial degradation of polychlorinated biphenyl compounds (PCBs) at a concentration of 100-200 mg/kg soil in contaminated environments, using natural, non-toxic, environmentally-acceptable compounds for application to such environments, such that PCB-contaminated environments are bioremediated by inducing a metabolic pathway in PCB-degrading microbes. Inoculated or indigenous PCB-degrading microbes, such as Arthrobacter strain B1B are induced to decontaminate the PCBs. Also disclosed are a plant and chemical screening assays for identifying plants that produce metabolites which promote PCB cometabolism. Further disclosed is a method for bioremediating PCB-contaminated environments in a commercially practical manner using l-carvone, a nontoxic and inexpensive chemical component of spearmint, for the in situ cleanup of PCB-contaminated soils, to induce Arthrobacter strain B1B to cometabolize and to substantially degrade PCBs.

Abstract: A composition and method of removing hydrocarbons from a contaminated sludge which comprises hydrocarbons, solid particles and water is disclosed. The method comprises the steps of providing a contaminated sludge including hydrocarbons and solid particles such that the hydrocarbons are bound to at least some of the solid particles; applying a treatment fluid to the contaminated sludge, the treatment fluid comprising water, a silicate, a nonionic surfactant, an anionic surfactant, a phosphate builder and a caustic compound; contacting the contaminated sludge with the treatment fluid for a time sufficient to remove the hydrocarbons from at least some of the solid particles; separating the hydrocarbons from the treatment fluid and from the solid particles; recovering the hydrocarbons; and recycling the treatment fluid by applying the treatment fluid to additional contaminated sludge.

Abstract: A process for removal of halide from a halide containing organic compound in a solvent, a process for simultaneous removal of halide from a halide containing organic compound and reduction of an oxygen containing organic compound in a solvent, a process for removal of halide from a halide containing organic compound, a process for reduction of an oxygen containing organic compound in a solvent, a system for removal of halide from a halide containing organic compound in a solvent, a system for simultaneous removal of halide from a halide containing organic compound and the reduction of an oxygen containing organic compound in a solvent, and a system for reducing an oxygen containing organic compound in a solvent are disclosed.

Abstract: An apparatus and method for anaerobic biodegradation, bioremediation or bioprocessing of hydrocarbons dissolved in an aqueous matrix, such as wastewater, groundwater, or slurry. Dissolved alkanes (saturated hydrocarbons), alkenes (unsaturated hydrocarbons), aromatic hydrocarbons and/or halogenated hydrocarbons are metabolized or cometabolized. In one form, the invention involves introducing an aqueous stream comprising at least one dissolved aromatic hydrocarbon (such as benzene, toluene, ethylbenzene, o-xylene, m-xylene, p-xylene, phenol, o-cresol, m-cresol, or p-cresol) and a dissolved oxide of nitrogen ?such as nitrate (NO.sub.3.sup.-), nitrite (NO.sub.2.sup.-), nitric oxide (NO) and nitrous oxide (N.sub.2 O)!to a reactor, and operating said reactor under conditions that support denitrification of the aromatic hydrocarbon.

Abstract: Method for the regeneration of active carbon and polymeric adsorbents having oxidizable, organic pollutants adsorbed thereon by electrochemical and chemical means and apparatus therefor. The method involves a desorption step and a decomposition step. Desorption is accomplished in one embodiment by flowing an aqueous stream at a preselected pH through the adsorbent material. Generally, decomposition is accomplished by contacting an aqueous stream containing an organic pollutant with hydroxyl radicals. Sequential or simultaneous desorption and decomposition can also take place during electrolysis in an electrolytic cell. During decomposition the active carbon can be made a carbon bed electrode of the cell. Electrolysis to produce peroxide can take place in the presence of a transition metal or a chelate of a transition metal while feeding an oxygen containing gas to the electrolysis cell.

Abstract: A process for the destruction of organic compounds selected from the group consisting of nitriles, aromatics, heteroaromatics, amides, organic acids, aldehydes and alcohols from wastewater, comprising contacting volatilized wastewater with a catalyst at an elevated temperature in the absence of added oxygen, so as to convert volatile organic compounds and ammonia to a mixture comprising hydrogen and carbon dioxide which are separated and removed from the stream, yielding a purified aqueous stream, substantially free of organic compounds.

Abstract: Butane-utilizing bacteria are used to degrade hydrocarbon pollutants such as trichloroethene (TCE). In-situ or ex-situ techniques may be used to reduce or eliminate hydrocarbon pollutants from liquid, gas and solid sources. In a preferred embodiment, TCE concentrations in various aqueous environments are reduced by contacting a contaminated water source with butane-utilizing bacteria in the presence of oxygen to degrade the TCE by cometabolism or direct metabolism. Suitable butane-utilizing bacteria include Pseudomonas, Variovorax, Nocardia, Chryseobacterium, Comamonas, Acidovorax, Rhodococcus, Aureobacterium, Micrococcus, Aeromonas, Stenotrophomonas, Sphingobacterium, Shewanella, Phyllobacterium, Clavibacter, Alcaligenes, Gordona, Corynebacterium and Cytophaga. The butane-utilizing bacteria have relatively low TCE toxicity in comparison with conventional methane-utilizing bacteria, and demonstrate an improved ability to degrade TCE.

Abstract: Treatment of halogenated hydrocarbon contaminants in groundwater is accomplished by passing the water through a bed of granular iron (43). An electrical circuit (47) is promoted for providing electrons for reducing the contaminant. The circuit may be made using a DC supply, by configuring an electrolytic circuit, or by providing a layer of a second metal such as zinc placed next to the iron bed, thereby creating a galvenic circuit.

Abstract: Arsenic and TOC are removed from drinking water or wastewaters by use of finely-divided metallic iron in the presence of powdered elemental sulfur or other sulfur compounds such as manganese sulfide, followed by an oxidation step. A premix may be produced for this process, by adding the iron, sulfur and oxidizing agent to water in a predetermined pH range. The iron and sulfur are mixed for a period of time dependent upon the temperature and pH of the water and the presence of complexing or sequestering minerals and organic acids in the water. An oxidizing agent is added to the mixture and agitating is continued. In a preferred embodiment the oxidizing agent is hydrogen peroxide. Water is decanted from the mixture after a sufficient reaction time, to produce a concentrated premix. This premix can be added to water intended for drinking or to industrial effluents containing toxic materials.

Abstract: A method of remediating water or soil contaminated with contaminants including one or more halogenated, phenyl related biphenyl related, triazine related, and petroleum related compounds includes reacting the contaminated water or soil with an oxidant, and one or more metals in elemental or alloy form until essentially all of the contaminants has been decomposed and the water or soil is essentially free of the contaminants.

Abstract: A photocatalyst composition containing a substantially non-oxidizable binder which allows large amounts of photocatalytic particles to be adhered to a surface. Upon application to a surface, the composition dries or cures to form an adherent, abrasion-resistant, thermostable, and photocatalytic coating.

Abstract: A method for efficient, economical and rapid remediation of aromatic hydrocarbons, and especially polycyclic aromatic hydrocarbons (PAHs), in contaminated materials, such as soils, sludges, tars, sands and liquids using catalysts in conjunction with ozone, oxidants and surfactants. The method uses multistage catalytic oxidation to convert aromatic hydrocarbons into innocuous, biodegradable, or easily decomposed compounds such as carbon dioxide and carbonyl compounds, including but not limited to aldehydes, ketones, quinones and carboxylic acids. The method may be employed to treat dry and wet contaminated samples of large tonnage and offers an excellent alternative to incineration.

Abstract: A process for the decontamination of a medium including a particulate material contaminated with one or more organic species and one or more metal species, the process including the steps of: (1) treating said medium by breaking down the organic species by or through the action of microbial agents, (2) treating the medium with microbially produced sulfuric acid so as to solubilize and leach the metal species as a metal sulfate, (3) treating the leached metal sulfate by a bioprecipitation process which converts the said sulfate into one or more insoluble metal sulfides and hydrogen sulfide, (4) separating the hydrogen sulfide from the one or more insoluble metal sulfides and (5) oxidizing the separated hydrogen sulfide to form a reusable source of a sulfur-containing ingredient.

Abstract: A method for ex situ cleaning of contaminated soil using a closed system of heat-conductive solid-walled pipes embedded in the contaminated soil, the pipes being in communication with the heat source that heats and circulates air throughout the system of pipes, the method having the following steps of placing the contaminated soil in a heap on the pipes, substantially enclosing the soil heap with a vapor barrier, circulating heated air throughout the pipes to elevate the temperature of the surrounding soil to a temperature sufficient to cause vaporization of soil contaminants, extracting the vapor containing soil contaminants from the enclosed soil heap, and treating the vapor to remove contaminants and recycling the vapor.

Abstract: This invention relates to a process for the decomposition of material selected from the group consisting of organic compounds, inorganic compounds, or combinations thereof to compounds which are environmentally acceptable, or are amenable to further degradation by conventional disposal systems to produce environmentally acceptable products, which process comprises: (a) conveying an aqueous solution or an aqueous slurry of material into a reaction zone capable of withstanding the temperatures and pressures of decomposition of the material; (b) contacting the material in the reaction zone with aqueous sodium carbonate as a reactant in an amount effective to decompose the material under hot water or supercritical water oxidation conditions of between about 300.degree. and 600.degree. C. and a pressure of between about 20 and 400 atmospheres for between 0.

Abstract: A method for removing contaminants from fluids comprises contacting the fluid with an expanded material selected from popped corn, puffed rice and puffed wheat. The preferred expanded material is popped corn. The method is applicable to a wide range of organic and inorganic contaminants. Examples of contaminants include aromatic compounds such as polychlorinated biphenyls (PCBs), polychlorinated dibenzo furans (PCDFs), polychlorinated dibenzo dioxins (PCDDs), carbamates, sulphonamides, dichlorodiphenyltrichloroethane (DDT), 2,4-dichlorophenoxyacetic acid (2,4-D), other compounds such as carbon disulphide, ethylene glycol, pesticides, oils, wood preservatives, pulp and paper bleaching compounds. Other examples include inorganic compounds or organo-metallic compounds, e.g. those containing aluminum, antimony, barium, cadmium, cobalt, chromium, copper, iron, lead, mercury, molybdenum, nickel, silver, tin, titanium, vanadium and zinc.