Abstract: A method and apparatus for producing a carbon monoxide containing product in which cathode and anode sides of an electrically driven oxygen separation device are contacted with carbon dioxide and a reducing agent, respectively. The carbon dioxide is reduced to carbon monoxide through ionization of oxygen and the reducing agent lowers the partial pressure of oxygen at the anode side to partially drive oxygen ion transport within the device through the consumption of the oxygen and to supply heat. The lowering of oxygen partial pressure reduces voltage and therefore, electrical power required to be applied to the device and the heat is supplied to heat the device to an operational temperature and to the reduction of the carbon dioxide occurring at the cathode side. The device can be used as part of an integrated apparatus in which the carbon dioxide is supplied from a waste stream of a process plant.

Abstract: A layered structure can be formed having immobilized or segregated pH buffering groups that can be used to separate carbon dioxide or other gases. The pH buffering groups can be immobilized within a matrix, confined within a gel, or segregated by a semi-permeable membrane. The pH buffering groups can be configured to increase the efficiency of the system by maintaining a desirable pH profile within the cell and to permit the flow of the carbon-containing ions within the system while controlling diffusion of protons and/or hydroxyl ions.

Abstract: The present invention relates to carbon dioxide sequestration, including processes in which group-2 silicates are used to remove carbon dioxide from waste streams to form corresponding group-2 carbonates and silica.

Abstract: This invention provides a process for producing a lithium secondary battery. The process comprises: (a) providing a positive electrode; (b) providing a negative electrode comprising a carbonaceous material capable of absorbing and desorbing lithium ions, wherein the carbonaceous material is obtained by chemically or electrochemically treating a laminar graphite material to form a graphite crystal structure having an interplanar spacing d002 of at least 0.400 nm as determined from a (002) reflection peak in powder X-ray diffraction; and (c) providing a non-aqueous electrolyte disposed between the negative electrode and the positive electrode to form the battery structure. This larger interplanar spacing (greater than 0.400 nm, preferably no less than 0.55 nm) implies a larger interstitial space between two graphene planes to accommodate a greater amount of lithium. The resulting battery exhibits an exceptionally high specific capacity, an excellent reversible capacity, and a long cycle life.

Abstract: Methods and apparatus relate to capturing carbon dioxide. A solution formed from metal ions combined with an amine reagent absorbs carbon dioxide from gas introduced into the solution. Subsequent electrolysis of the solution results in dissociation of complexes formed upon the carbon dioxide being absorbed. The electrolysis thus liberates the carbon dioxide for capture and regenerates the solution for reuse.

Abstract: A method for reducing carbon dioxide to one or more products is disclosed. The method may include steps (A) to (C). Step (A) may bubble the carbon dioxide into a solution of an electrolyte and a catalyst in a divided electrochemical cell. The divided electrochemical cell may include an anode in a first cell compartment and a cathode in a second cell compartment. The cathode generally reduces the carbon dioxide into the products. Step (B) may vary at least one of (i) which of the products is produced and (ii) a faradaic yield of the products by adjusting one or more of (a) a cathode material and (b) a surface morphology of the cathode. Step (C) may separate the products from the solution.

Abstract: A method for purification of carbon dioxide from a mixture of gases is disclosed. The method generally includes steps (A) and (B). Step (A) may bubble the gases into a solution of an electrolyte and a catalyst in an electrochemical cell. The electrochemical cell may include an anode in a first cell compartment and a cathode in a second cell compartment. The cathode generally reduces the carbon dioxide into one or more compounds. The anode may oxidize at least one of the compounds into the carbon dioxide. Step (B) may separate the carbon dioxide from the solution.

Abstract: A layered structure can be formed having immobilized or segregated pH buffering groups that can be used to separate carbon dioxide or other gases. The pH buffering groups can be immobilized within a matrix, confined within a gel, or segregated by a semi-permeable membrane. The pH buffering groups can be configured to increase the efficiency of the system by maintaining a desirable pH profile within the cell and to permit the flow of the carbon-containing ions within the system while controlling diffusion of protons and/or hydroxyl ions.

Abstract: An alkaline production system comprising an electrochemical unit comprising a hydrogen-oxidizing anode, a cathode compartment comprising a cathode and a hydrogen delivery system configured to deliver hydrogen gas to the anode, wherein the system configured to sequester carbon dioxide with the cathode electrolyte; and methods thereof. In another embodiment, a system comprising a hydrogen-oxidizing anode in communication with a cathode electrolyte comprising bicarbonate ion; and an hydrogen delivery system configured to deliver hydrogen gas to the anode; and methods thereof.

Abstract: A low-energy electrochemical method and system of forming bicarbonate ion solutions in an electrochemical cell utilizing carbon dioxide in contact with an electrolyte contained between two ion exchange membranes in an electrochemical cell. On applying a low voltage across an anode and cathode in electrical contact with the ion exchange membranes, bicarbonate ions form in the electrolyte without forming a gas, e.g., chlorine or oxygen at the electrodes.

Abstract: A low-voltage, low-energy electrochemical system and method of removing protons and/or producing a base solution comprising hydroxide and carbonate/bicarbonate ions, utilizing carbon dioxide in a cathode compartment that is partitioned into a first cathode electrolyte compartment and a second cathode electrolyte compartment such that liquid flow between the cathode electrolyte compartments is possible, but wherein gaseous communication between the cathode electrolyte compartments is restricted. Carbon dioxide gas in one cathode electrolyte compartment is utilized with the cathode electrolyte in both compartments to produce the base solution with less that 3V applied across the electrodes.

Abstract: A low-energy method and system of forming hydroxide ions in an electrochemical cell. On applying a low voltage across the anode and cathode, hydroxide ions form in the electrolyte containing the cathode, protons form at the anode but a gas e.g. chlorine or oxygen does not form at the anode.

Abstract: The invention relates to a reactor for the electrochemical treatment of biomass, including at least two flat surface electrodes positioned equidistantly over the entire surface and separated by less than 1 mm, the space between said electrodes being occupied by a electrolytic solution. Preferably, at least one of the electrodes is an anode and at least one of the electrodes is a cathode. The anode is preferably made from a material selected from among vanadium, selenium, gold, silver, nickel, graphite, graphite galvanised with platinum and graphite galvanised with palladium. The invention also relates to the use of said reactor in electrooxidation reactions involving biomass, particularly polysaccharides, in the production of organic compounds, water electrolysis, hydrogen production or the production of electrochemical cells.

Abstract: Deposition of nanoparticles onto carbon surfaces is described. Metal and/or metal oxide ions are deposited on a carbon surface by electrodeposition, such as by immersing a carbon and an anode in a salt bath, and applying a number of electrical pulses having a defined pulse width. The size, coverage density, and metallic composition of the nanoparticles may be affected by the pulse width of the electrical pulses, the number of electrical pulses, and the chemical composition of the salt bath, respectively. The carbon may be anodized before electrodeposition. If the carbon is a carbon precursor, after electrodeposition, the carbon precursor is carbonized to form a carbon. After electrodeposition, the carbon may be activated to form an activated carbon. The nanoparticles may serve as catalysts for activation rugosity of mesoporous carbons. The catalytically activated carbon materials may be used in all manner of devices that contain carbon materials.

Abstract: An electrochemical system comprising a cathode electrolyte comprising added carbon dioxide and contacting a cathode; and a first cation exchange membrane separating the cathode electrolyte from an anode electrolyte contacting an anode; and an electrochemical method comprising adding carbon dioxide into a cathode electrolyte separated from an anode electrolyte by a first cation exchange membrane; and producing an alkaline solution in the cathode electrolyte and an acid.

Abstract: Carbon nanotubes, a method for preparing the same and an element using the same are provided. The method for preparing carbon nanotubes includes synthesizing carbon nanotubes from carbon source using an arc-discharge method in the presence of catalysts and promoter, wherein the promoter contains an element capable of reducing the surface energy of carbon nanotubes. Carbon nanotubes with high purity and narrow diameter distribution can thus be prepared.

Abstract: In an apparatus for surface-treating a carbon fiber, wherein the carbon fiber is heated by resistive heating, a carbon-containing gas is disposed on the carbon fiber, and carbon nanotubes are grown on a surface of the carbon fiber.

Abstract: An apparatus for forming a carbon nanotube sheet is provided. The apparatus includes a bath and a driving unit wherein the bath has a bottom surface and is configured to contain a carbon nanotube colloidal solution. The bottom surface is capable of having an array of capillary tubes. The driving unit is configured to drive at least a part of the carbon nanotube colloidal solution out of the bath through the array of capillary tubes.

Abstract: The oxalic acid aqueous solution filled in an electrolytic tank is electrolyzed with an electrolyzer to produce carbonic acid gas, while ultrasonic wave from an ultrasonic generator is applied to the produced carbonic acid gas bubbles, to form micro bubbles, which is dissolved in said oxalic acid aqueous solution, so as to easily produce carbonic acid gas solution with micro carbonic acid gas bubbles dissolved at a low cost; said carbonic acid gas solution can substitute carbonated spring.

Abstract: A mold is for obtaining, on a substrate, an array of carbon nanotubes with a high control of their positioning. The mold includes a first layer of a first preset material having a surface having in relief at least one first plurality of projections having a free end portion with a substantially pointed profile.

Abstract: An oxidizing device and an oxidizing method for oxidizing a carbon-containing component in a gaseous mixture containing H2O and the carbon-containing component are disclosed having a proton conductive body and an electrode member placed on the proton conductive body. The electrode member has an anode electrode and a cathode electrode held in contact with each other and the proton conductive body has electric conductivity of 0.01 Scm?1 or more at a temperature of 400° C. or less. The anode electrode separates a proton (H+) from H2O at a boundary portion between the anode electrode and the proton conductive body to facilitate a reaction to introduce the proton into the proton conductive body. The cathode electrode facilitates a reduction reaction in the presence of the proton supplied from the proton conductive body at a boundary portion between the cathode electrode and the proton conductive body.

Abstract: Disclosed are methods for forming carbon nano-onions. The methods include annealing a carbon nanodiamond starting material in an inert atmosphere. The method can be carried out at ambient pressure. Also disclosed are methods for functionalizing carbon nano-onions. For instance, carbon nano-onions can be functionalized so as to be soluble in aqueous or organic solvents, as desired. Also disclosed are methods for separating mixtures of carbon nano-onions. In particular, mixtures of carbon nano-onions can be separated from one another based upon differences in electrochemical characteristics of the different nano-onions.

Abstract: Coaxial disk armatures, counter-rotating through an axial magnetic field, act as electrolysis electrodes and high shear centrifugal impellers for an axial feed. The feed can be carbon dioxide, water, methane, or other substances requiring electrolysis. Carbon dioxide and water can be processed into syngas and ozone continuously, enabling carbon and oxygen recycling at power plants. Within the space between the counter-rotating disk electrodes, a shear layer comprising a fractal tree network of radial vortices provides sink flow conduits for light fractions, such as syngas, radially inward while the heavy fractions, such as ozone and elemental carbon flow radially outward in boundary layers against the disks and beyond the disk periphery, where they are recovered as valuable products, such as carbon nanotubes.

Abstract: A first aqueous solution filled in an electrolytic cell (2) is electrolyzed by applying DC voltage between the electrodes 7a and 7b in said electrolytic cell 2, to form an oxidation field short of electrons in said aqueous solution; and then, a second aqueous solution with carboxylic acid dissolved in it is mixed into the first aqueous solution in oxidation field state, so that the first aqueous solution in oxidation field state obtains electrons and is deoxidized, and the carboxylic acid is oxidized, to produce carbonic acid gas in said aqueous solution. Therefore, the present invention can be used to produce carbonic acid gas solution at a low cost easily.

Abstract: Carbon dioxide can be separated from gas streams using ion exchange, such as in an electrochemical cell. An anion exchange membrane can be configured to increase the efficiency of the system and to permit the flow of the carbon-containing ions within the system while reducing diffusion of protons and/or hydroxyl ions. A gas stream containing carbon dioxide can be introduced to the system on the cathode side, while a source of hydrogen-containing molecules can be introduced on the anode side. Operation of the system can separate the carbon dioxide from the gas stream and provide it at a separate outlet.

Abstract: Methods of purifying samples are provided that are capable of removing carbonaceous and noncarbonaceous impurities from a sample containing a carbon material having a selected structure. Purification methods are provided for removing residual metal catalyst particles enclosed in multilayer carbonaceous impurities in samples generate by catalytic synthesis methods. Purification methods are provided wherein carbonaceous impurities in a sample are at least partially exfoliated, thereby facilitating subsequent removal of carbonaceous and noncarbonaceous impurities from the sample. Methods of purifying carbon nanotube-containing samples are provided wherein an intercalant is added to the sample and subsequently reacted with an exfoliation initiator to achieve exfoliation of carbonaceous impurities.

Abstract: The present invention provides a process for producing fine particles of a salt, hydroxide or oxide, wherein when producing the salt, hydroxide or oxide by electrodialysis using anion exchange membranes and cation exchange membranes, a conductive liquid acting as a poor solvent for the salt, hydroxide or oxide which is produced in a concentration chamber is used as a concentration chamber solution, as well as the fine particles of the salt, hydroxide or oxide which are produced by the above process.

Abstract: This invention provides a process for producing a lithium secondary battery. The process comprises: (a) providing a positive electrode; (b) providing a negative electrode comprising a carbonaceous material capable of absorbing and desorbing lithium ions, wherein the carbonaceous material is obtained by chemically or electrochemically treating a laminar graphite material to form a graphite crystal structure having an interplanar spacing d002 of at least 0.400 nm as determined from a (002) reflection peak in powder X-ray diffraction; and (c) providing a non-aqueous electrolyte disposed between the negative electrode and the positive electrode to form the battery structure. This larger interplanar spacing (greater than 0.400 nm, preferably no less than 0.55 nm) implies a larger interstitial space between two graphene planes to accommodate a greater amount of lithium. The resulting battery exhibits an exceptionally high specific capacity, an excellent reversible capacity, and a long cycle life.

Abstract: A method of producing nano-scaled graphene platelets with an average thickness smaller than 30 nm from a layered graphite material. The method comprises (a) forming a carboxylic acid-intercalated graphite compound by an electrochemical reaction which uses a carboxylic acid as both an electrolyte and an intercalate source, the layered graphite material as an anode material, and a metal or graphite as a cathode material, and wherein a current is imposed upon the cathode and the anode at a current density for a duration of time sufficient for effecting the electrochemical reaction; (b) exposing the intercalated graphite compound to a thermal shock to produce exfoliated graphite; and (c) subjecting the exfoliated graphite to a mechanical shearing treatment to produce the nano-scaled graphene platelets. Preferred carboxylic acids are formic acid and acetic acid.

Abstract: It is an object of the present invention to provide an oxygen reduction electrode which provides four-electron reduction reaction with high selectivity in the reaction of reducing oxygen. The present invention involves a method of manufacturing an electrode for reducing oxygen used for four-electron reduction of oxygen, having (1) a first step wherein a charcoal-based material is obtained by carbonization of a starting material comprising a nitrogen-containing synthetic polymer, and (2) a second step wherein the electrode for reducing oxygen is manufactured using an electrode material comprising the charcoal-based material.

Abstract: A carbon dioxide negative method of manufacturing renewable hydrogen and trapping carbon dioxide from the air or gas streams is described. Direct current renewable electricity is provided to a water electrolysis apparatus with sufficient voltage to generate hydrogen and hydroxide ions at the cathode, and protons and oxygen at the anode. These products are separated and sequestered and the base is used to trap carbon dioxide from the air or gas streams as bicarbonate or carbonate salts. These carbonate salts, hydrogen, and trapped carbon dioxide in turn can be combined in a variety of chemical and electrochemical processes to create valuable carbon-based materials made from atmospheric carbon dioxide. The net effect of all processes is the generation of renewable hydrogen from water and a reduction of carbon dioxide in the atmosphere or in gas destined to enter the atmosphere.

Abstract: This invention relates to technology of carbographite materials, in particular, to production of oxidized graphite for making low foaming temperature foamed graphite, which is used for manufacturing flexible foil, fireproof materials, water-purification sorbents, materials for cleaning up spills of petroleum products, and so on. The method for producing oxidized low foaming temperature graphite comprises the stages of (a) preparing a mixture based on graphite particles and at least one aqueous solution of an acid; (b) activating the surface of said graphite particles to produce acid-containing functional groups on the surface of the particles; (c) treating the graphite particles to produce a graphite intercalation compound; (d) washing said compound with water; (e) drying said compound, and heat-treating it to produce foamed graphite, wherein stage (b) and (c) are carried out by electrochemical treatment at a quantity of electricity within 300 to 600 mA·hour/g of graphite.

Abstract: An electrochemical gas generator is provided including an electrolysis cell (1) with a gas-impermeable housing, which is closed by a gas-permeable membrane (2) for the discharge of the test gas or calibrating gas CO. A chemically inert cathode (5) formed of a noble metal, a mixture of noble metals or a material containing carbon, is in direct contact with an electrolyte (7). An anode (4) formed of a noble metal, a mixture of noble metals or a material containing carbon, is in direct contact with a mesoxalic acid salt, the mesoxalic acid salt being in direct contact with the electrolyte (7). A control unit (6) is provided that also acts as a power source and is connected to the electrodes (4, 5).

Abstract: A conductive diamond electrode including a conductive substrate comprising a carbonaceous material, a conductive diamond catalyst layer formed on a surface of the conductive substrate, and a carbon fluoride formed on an exposed portion present on the surface of the conductive substrate. The formed carbon fluoride prevents the conductive substrate from contacting with an electrolytic solution, thereby suppressing corrosion of the substrate. A long life of the electrode can be attained.

Abstract: A method of producing magnetic metal-filled carbon nanocapsules. An arc chamber comprising a graphitic anode and a composite graphitic cathode containing at least one kind of magnetic metal or it's derivatives is provided, before introducing an inert gas into the arc chamber, applying a voltage across the cathode and the anode by a pulse current, the voltage sufficient, to generate a carbon arc reaction between the cathode and the anode, and finally collecting a deposit formed on the cathode.

Abstract: Methods for conditioning the membrane electrode assembly of a direct methanol fuel cell (“DMFC”) are disclosed. In a first method, an electrical current of polarity opposite to that used in a functioning direct methanol fuel cell is passed through the anode surface of the membrane electrode assembly. In a second method, methanol is supplied to an anode surface of the membrane electrode assembly, allowed to cross over the polymer electrolyte membrane of the membrane electrode assembly to a cathode surface of the membrane electrode assembly, and an electrical current of polarity opposite to that in a functioning direct methanol fuel cell is drawn through the membrane electrode assembly, wherein methanol is oxidized at the cathode surface of the membrane electrode assembly while the catalyst on the anode surface is reduced. Surface oxides on the direct methanol fuel cell anode catalyst of the membrane electrode assembly are thereby reduced.

Abstract: A device as described for the generation of high purity carbon dioxide (CO2) and hydrogen (H2) by electrochemical decomposition of aqueous solutions of liquid and solid organic acids. A d.c. power source is used to apply a pre-selected current to an electrochemical cell, consisting of an ion permeable membrane and two electrodes. The generation rate of CO2 and H2 are continuous and proportional to the applied current; it can be stopped instantaneously by interrupting the current. Small battery operated generators can produce propellant CO2 and H2 to deliver fluids from containers other uses include the creation of anaerobic environments in incubation chambers.

Abstract: A system and method for producing dry gas, such as methane or carbon dioxide, incorporates an electrochemical device that removes water and hydrogen from a mixed gas stream. The electrochemical device uses one electrochemical cell to strip hydrogen and water from the mixed gas stream and a second electrochemical cell, combined with a dry feed stream, to remove any residual water from the mixed stream and produce pure, dry gas.

Abstract: The invention of present application relates to a method for enabling a hybrid carbon nanotube having an arbitrary composition ratio to be readily manufactured, and the hybrid carbon nanotube. A method for manufacturing a hybrid carbon nanotube, which comprises immersing a carbon nanotube having open pores in a solution having a dopant substance dissolved therein to effect a doping reaction, thereby preparing a hybrid carbon nanotube comprising a carbon nanotube and a dopant substance introduced therein.

Abstract: The present invention is directed to a process and apparatus for producing synthesis gas by electrolysis. The process for producing synthetic gas is heat exchanged between reactants and reaction products of at least one reaction product carried out using textile micro-hollow fibers having non-activated surfaces as heat exchangers as solid electrolytes, the inside and outside surfaces which carry the anodes and cathodes, respectively. The apparatus for producing synthesis gas by electrolysis comprises a multitude of stacked textiles micro-hollow fibers as solid electrolytes, the inside and outside surfaces of which carry the anodes and cathodes, respectively, wherein the ends of the micro-hollow fibers are bound into a frame, and a pressure housing accommodating the stacks is made from a ferromagnetic material and has a partly enameled surface.

Abstract: Intercalated graphite flake is prepared having enhanced exfoliation characteristics in terms of at least one of reduced exfoliation temperature and increased expanded volume (also referred to as “worm volume”). The method entails contacting graphite flake with an organic expansion aid either before immersing in an aqueous intercalant solution or by dissolving the expansion aid in the aqueous intercalant solution prior to subjecting graphite flake to an electrolytic oxidation treatment therein. The graphite flake is subjected to electrolytic oxidation to provide intercalated graphite flake. Then, the intercalated graphite flake is recovered from the bulk of the intercalant solution and is preferably washed and further treated with a suitable surfactant in order to reduce the exposed gallery acids on the subsequently dried flake.

Abstract: Intercalated graphite flake is prepared having enhanced exfoliation characteristics in terms of at least one of reduced exfoliation temperature and increased expanded volume (also referred to as “worm volume”). The method entails contacting graphite flake with an organic expansion aid either before immersing in an aqueous intercalant solution or by dissolving the expansion aid in the aqueous intercalant solution prior to subjecting graphite flake to an electrolytic oxidation treatment therein. The graphite flake is subjected to electrolytic oxidation to provide intercalated graphite flake. Then, the intercalated graphite flake is recovered from the bulk of the intercalant solution and is preferably washed and further treated with a suitable surfactant in order to reduce the exposed gallery acids on the subsequently dried flake.

Abstract: This invention discloses regeneration methods to remove carbon monoxide (CO) from reformate fuel using an adsorption and electro-catalytic oxidation (ECO) approach. One method of the invention comprises a first ECO cell and a second ECO cell, and the other method comprises a first ECO cell and a first charge storage device. Both methods eliminate the requirement of an external power supply that leads to higher cost, additional power consumption and more processor complexity for the CO removal processor.

Abstract: Methods and devices for transforming less desirable chemical species into more desirable or useful chemical forms are disclosed. The specifications can be used to treat pollutants into more benign compositions and to produce useful chemicals from raw materials and wastes. The methods and devices disclosed utilize electrical current induced by electromagnetic field and high surface area formulations. The invention can also be applied to improve the performance of existing catalysts and to prepare novel devices.

Abstract: Binary and ternary electrocatalysts are provided for oxidizing alcohol in a fuel cell. The binary electrocatalyst includes 1) a substrate selected from the group consisting of NiWO4 or CoWO4 or a combination thereof, and 2) Group VIII noble metal catalyst supported on the substrate. The ternary electrocatalyst includes 1) a substrate as described above, and 2) a catalyst comprising Group VIII noble metal, and ruthenium oxide or molybdenum oxide or a combination thereof, said catalyst being supported on said substrate.

Abstract: CMPO is safely, reliably and rapidly decomposed under mild conditions. A CMPO-containing substance is emulsified in an electrolyte comprising an oxidation promoter (silver ion) by an emulsifier in an emulsifying tank, this electrolyte comprising the CMPO-containing substance is supplied to an anode chamber, and an electrolytic oxidation reaction is performed by passing an electric current. By emulsifying the CMPO-containing substance, the surface area of CMPO in contact with electrolyte is increased, and electrolytic decomposition is thereby promoted. As sufficient CMPO decomposition is not obtained by passing the emulsion only once through an electrolysis tank 1, a batch oxidation method is employed wherein an anolyte is recirculated by a recirculating pump 3a through the anode chamber, a constant temperature bath 7a and an emulsifying tank 6, so that electrolysis is performed with the CMPO-containing substance permanently emulsified in the electrolyte.

Abstract: There are disclosed a process for the electrochemical decomposition of organic pollutants in an acidic solution to carbon dioxide performed in a electrochemical system comprising a working electrode and an auxiliary electrode with oxygen at ambient temperature and at a reductive potential or current, wherein the working electrode used is a graphite-containing electrode.

Abstract: A graphite intercalation compound is disclosed in which formic acid (HCOOH) is the intercalate. The GIC may be formed by an electrochemical process using formic acid solution as both the electrolyte and as the intercalate source. The resulting formic acid GIC may be expanded by rapid heating to produce an expanded graphite product that in turn may be mechanically processed into flexible graphite.

Abstract: Electrolyzer comprising at least one elementary cell divided into electrolyte compartments by cation-exchange membranes, said compartments are provided with a circuit for feeding electrolytic solutions and a circuit for withdrawing electrolysis products, said cell is equipped with a cathode and a hydrogen-depolarized anode assembly forming a hydrogen gas chamber fed with a hydrogen-containing gaseous stream, characterized in that said assembly comprises a cation-exchange membrane, a porous, flexible electrocatalytic sheet, a porous rigid current collector having a multiplicity of contact points with said electrocatalytic sheet, said membrane, sheet and current collector are held in contact together by means of pressure without bonding.

Abstract: An electrochemical cell/electrolyte/mediator combination for the efficient destruction of organic contaminants using metal salt mediators in a sulfuric acid electrolyte, wherein the electrodes and mediator are chosen such that hydrogen gas is produced at the cathode and no cell membrane is required.