Abstract: In the disclosed electrochemical cell for the production of an alkaline solution of peroxide, especially on-site production, the electrolyte is divided into an aqueous alkaline catholyte and an aqueous alkaline anolyte, and the cathode is a gas-diffusion electrode. The active material of the electrolyte side of the gas-diffusion cathode comprises a particulate catalyst support material having a surface area of about 50 to about 2000 m.sup.2 /g, and, deposited on the particles of this support material, 0.1 to 50 weight-%, based on the weight of the active layer, of gold or gold alloy particles having an average size >40 but less than about 200 .ANG.. These gold or gold alloy particles are substantially selectively catalytic for the reduction of oxygen to peroxide (e.g. HOO.sup..crclbar.). The electrolyte flow patterns are designed to avoid loss of peroxide resulting from oxidation at the anode. In the operation of the cell, a product with a hydroxyl:perhydroxyl ratio lees than 2:1 can be obtained.

Abstract: In the disclosed electrochemical cell for the production of an alkaline solution of peroxide, especially on-site production, the electrolyte is divided into an aqueous alkaline catholyte and an aqueous alkaline anolyte, and the cathode is a gas-diffusion electrode. The active material of the electrolyte side of the gas-diffusion cathode comprises a particulate catalyst support material having a surface area of about 50 to about 2000 m.sup.2 /g, and, deposited on the particles of this support material, 0.1 to 50 weight-%, based on the weight of the active layer, of gold or gold alloy particles having an average size >40 but less than about 200.ANG.. These gold or gold alloy particles are substantially selectively catalytic for the reduction of oxygen to peroxide (e.g. HOO.sup..crclbar.). The electrolyte flow patterns are designed to avoid loss of peroxide resulting from oxidation at the anode. In the operation of the cell, a product with a hydroxyl:perhydroxyl ratio less than 2:1 can be obtained.

Abstract: In the disclosed electrochemical cell for the production of an alkaline solution of peroxide, especially on-site production, the electrolyte is divided into an aqueous alkaline catholyte and an aqueous alkaline anolyte, and the cathode is a gas-diffusion electrode. The active material of the electrolyte side of the gas-diffusion cathode comprises a particulate catalyst support material having a surface area of about 50 to about 2000 m.sup.2 /g, and, deposited on the particles of this support material, 0.1 to 50 weight-%, based on the weight of the active layer, of gold or gold alloy poly-crystal particles having an average size .gtoreq.5 but less than about 20 nanometers. These poly-crystal gold or gold alloy particles have a structure consisting essentially of combined individual monocrystals and are substantially selectively catalytic for the reduction of oxygen to peroxide ion or hydrogen peroxide (e.g. HOO.sup..theta.).

Abstract: The gas-sensing electrodes prepared according to this invention are specifically designed for cells which operate in a current-limited mode, i.e. at current densities well below 20 mA/cm.sup.2. Such cells are particularly useful to measure or detect a gaseous component of a gaseous environment or stream, provided the gaseous component can be electrochemically oxidized or reduced. In an alkaline, metal-oxygen cell for example, an electrode of this invention can be used as an oxygen cathode. The electrode is prepared by:(a) bringing an exposed face of a self-supporting, electrically-conducting sheet of fibrous or sintered-particle material having a thickness of at least about 30 .mu.m and a flexural strength of at least 2000 kPa into contact with an electrolyte containing ions of a catalytic metal, the electrolyte also being in contact with a counterelectrode,(b) applying a pulsed-D.C.

Abstract: Gas-diffusion electrodes (GDE's) suitable for use with a solid polymer electrolyte (s.p.e.), particularly in s.p.e. fuel cells, which GDE's provide unusually highly efficient use of noble or precious electrocatalytic metals, are obtained by starting with a GDE which is essentially fully fabricated except for electrocatalytic metal treatment and s.p.e. treatment, e.g. a carbon GDE having a gas-permeable hydrophobic face and a particulate carbon-containing catalytic face. This untreated GDE is treated bya. impregnating an s.p.e. solutuion into the catalytic face until the solution penetrates part way into the cross-section of the GDE, especially into the carbon particulate or other support material, but not as far as the hydrophobic, gas permeable face,b. inserting the thus-treated GDE and a counterelectrode into a plating bath containing, for example, M.sup.+, M.sup.++, and/or M.sup.+++ ions, where M is a metal of Group VIII or I-B of the Periodic Table, andc.