Patent classifications
B01J23/652
Compound, and method for producing the same
The present invention provides a method for producing a compound represented by formula (2), comprising at least a step of preparing a compound represented by formula (1) and a step of reacting the compound represented by formula (1) with a hydrogen source using a catalyst, ##STR00001##
wherein R.sup.1 and R.sup.2 are each independently an alkyl group.
PHOTOCATALYST COMPOSITION, IODINE SOLUTION, PHOTOCATALYST DISPERSION LIQUID, ANTIBACTERIAL ACTIVATION METHOD, AND ANTIBACTERIAL ACTIVATION APPARATUS
The present disclosure provides a photocatalyst composition that has excellent antibacterial properties in a bright place and can suppress a decrease in antibacterial action over time in a dark place. The present disclosure provides a photocatalyst composition containing a photocatalyst particle, a co-catalyst, and iodine or a water-soluble iodine compound, characterized in that the iodine is formed from an iodide ion by photocatalyst activity generated by the photocatalyst particle receiving light.
Process for production of adipic acid from 1,6-hexanediol
Processes are disclosed for the conversion of 1,6-hexanediol to adipic acid employing a chemocatalytic reaction in which 1,6-hexanediol is reacted with oxygen in the presence of particular heterogeneous catalysts including at least one of platinum or gold. The metals are preferably provided on a support selected from the group of titania, stabilized titania, zirconia, stabilized zirconia, silica or mixtures thereof, most preferably zirconia stabilized with tungsten. The reaction with oxygen is carried out at a temperature from about 100? C. to about 300? C. and at a partial pressure of oxygen from about 50 psig to about 2000 psig.
VISIBLE LIGHT-ACTIVATED PHOTOCATALYTIC COATING COMPOSITION AND AIR PURIFICATION FILTER
Disclosed is a visible light-activated photocatalytic coating composition comprising a visible light active photocatalytic material and an aqueous solvent.
Oxygen storage materials
The present invention is concerned with oxygen storage materials. In particular an oxygen storage material (OSM) is proposed which comprises a certain mixed oxide as the oxygen storage component. The oxygen storage material can be used in conventional manner in three-way catalysts or NOx-storage catalysts for example.
METHOD FOR PREPARING A CATALYZED FABRIC FILTER AND A CATALYZED FABRIC FILTER
A catalyzed fabric filter substrate and a method of preparing the substrate comprising the steps of a) providing a fabric filter substrate b) providing an aqueous impregnation liquid comprising an aqueous hydrosol of one or more catalyst metal precursor compounds dispersed on nanoparticles of an oxidic metal carrier, a surfactant and a dispersing agent selected from the group of primary amines; c) impregnating the fabric filter substrate with the impregnation liquid; and d) drying and thermal activating the impregnated fabric filter substrate at a temperature below 300? C. to convert the one or more metal compounds of the catalyst precursor to their catalytically active form.
Post treated silver catalysts for epoxidation
The present disclosure generally relates to a silver-based epoxidation catalyst. In certain embodiments, a method is provided for modulating the reactivity of the silver-based epoxidation catalyst, comprising the catalyst being post-treated with at least two different salt solutions. In some embodiments, the treatment results in the deposition of one or more metals onto the surface of the catalyst. In further embodiments, method is also provided of using the silver catalyst to generate an epoxide from an olefin.
Poison-Resistant Catalyst and Systems Containing Same
A poison-resistant catalytic converter includes a washcoat having a support material comprised of titania and/or silica and a plurality of platinum group metal particles disposed in the support material. The washcoat is disposed on a substrate having a plurality of cells that define respective apertures. The catalytic converter is resistant to poisoning from sulfur and phosphorous compounds while operating at low temperatures. Applications include spark ignited internal combustion engines in combined heat and power systems, vehicles, combustion turbines, boilers and other applications for utilities, industry and vehicle emissions control.
Photocatalyst
A photocatalyst is described that is suitable for converting molecular nitrogen into ammonia. The photocatalyst comprises a layered base material comprising 1 to 100 layers, the layered base material being selected from the group consisting of molybdenum disulfide, tungsten disulfide, molybdenum telluride, tungsten telluride, molybdenum selenide and tungsten selenide, a layered base material comprising 1 to 100 layers, the layered base material being selected from the group consisting of molybdenum disulfide, tungsten disulfide, molybdenum telluride, tungsten telluride, molybdenum selenide and tungsten selenide, and 0.1-10.0% by weight, relative to the weight of the base material, of one or more Group VI, VII, VIII, IX or X transition metals. The photocatalyst can further comprise 0.1-50.0% by weight, relative to the weight of the base material, of one or more semiconductor materials having an average particle size of 0.5-50.0 nm. The photocatalyst exhibits high catalytic efficiency without the need for high temperature and pressure. Also described is a process for the preparation of the photocatalyst, as well as uses of the photocatalyst for converting molecular nitrogen into ammonia.
Methods for operating polyethylene reactor systems
A method of operating a polyethylene reactor system includes feeding ethylene, an optional first comonomer, a diluent, and a chromium-based catalyst to a first polymerization reactor. The method further includes contacting ethylene and the comonomer with the catalyst in the first polymerization reactor to form a first product including a first polyethylene. The method further includes feeding the first product from the first polymerization reactor to a second polymerization reactor. The method further includes contacting ethylene and a second optional comonomer with catalyst from the first reactor in the second polymerization reactor to form a second product including the first polyethylene and a second polyethylene. The method further includes controlling one or both of a molecular weight or a breadth of molecular weight distribution of the second product by adjusting a rate of hydrogen fed to one or both of the first polymerization reactor or the second polymerization reactor.