Patent classifications
B01J35/612
Size-reversing materials for reforming in cyclic flow reactors
Systems and methods are provided for using size-reversing materials in vessels where direct heating is used to at least partially provide heat for reforming reactions under cyclic reforming conditions. An example of a size-reversing material is the combination of NiO and Al.sub.2O.sub.3. It has been discovered that size-reversing materials can undergo a phase transition that can assist with re-dispersion of metal at elevated temperatures. This can assist with maintaining catalytic activity for reforming over longer time periods in the presence of cyclic reforming conditions.
High porosity cerium and zirconium containing oxide
This disclosure generally relates to an oxide composition basically composed of cerium and zirconium that has exceptional and stable porosity, surface area and lattice oxygen mobility. The oxide composition can contain one or more other rare earth oxides other than cerium oxide. For example, some compositions can contain one or more of lanthanum oxide, yttrium oxide and neodymium oxide. The oxide composition can be useful as a catalyst, catalyst support, sensor applications and combinations thereof.
Catalyst Compositions and Their Use in Aromatic Alkylation Processes
Catalyst compositions comprising a zeolite and a mesoporous support or binder are disclosed. The mesoporous support or binder comprises a mesoporous metal oxide having a particle diameter of greater than or equal to 20 m at 50% of the cumulative pore size distribution (d50). Also disclosed are processes for producing a mono-alkylated aromatic compound (e.g., ethylbenzene or cumene) which exhibit improved yield of the mono-alkylated aromatic compound using alkylation catalysts comprising one or more of these catalyst compositions.
EFFICIENT BIOMASS CARBON-BASED SOLID ACID ESTERIFICATION CATALYST FOR PRODUCING BIODIESEL
A method for producing biodiesel using a sulfonated, carbonaceous catalyst produced from rice husk, Moringa seeds, or algae biomass, a method for producing the catalyst, and the catalyst itself.
ONE STEP LIQUID-TO-METAL HIGH SURFACE AREA CATALYSTS VIA LOW TEMPERATURE REDUCTION
High surface area metal catalysts, and methods of making and using the same, are described.
A Catalyst Composition for Different Reforming Techniques
The present invention provides a catalyst composition comprising different metal oxides wherein the catalyst composition comprising Ce, Cr and Ni oxides and a process for preparation thereof. The catalyst composition is used for different reforming techniques for the production of syn gas (CO+H.sub.2) at the same time this material can be used in fuel cell as a anode for power generation as this synthesized material is having good thermal stability and can sustain various redox reaction cycles also.
EXHAUST GAS-PURIFYING THREE-WAY CATALYST AND METHOD FOR PRODUCING SAME, AND INTEGRAL STRUCTURE TYPE EXHAUST GAS-PURIFYING CATALYST
Provided is, for example, an exhaust gas-purifying three-way catalyst which is suppressed in particle growth due to sintering of a catalytically active component on a carrier in exposure to a high temperature and thus is enhanced in purification performance, and a method for producing the same, as well as an integral structure type exhaust gas-purifying catalyst using the same.
The exhaust gas-purifying three-way catalyst of the present invention includes a composite particle which contains a base material particle having a pore size of 100 to 650 nm as measured by a mercury intrusion method and a catalytically active particle of a platinum group element supported on the base material particle, in which a content proportion of the catalytically active particle is 0.001 to 30% by mass in total in terms of metal of the platinum group element, based on a total amount of the composite particle.
CATALYST CONTAINING LF-TYPE B ACID AND METHOD FOR PREPARING ETHYLENE USING DIRECT CONVERSION OF SYNGAS
A catalyst containing LF-type B acid preparing ethylene using direct conversion of syngas is a composite catalyst and formed by compounding component A and component B in a mechanical mixing mode. The active ingredient of the component A is a metal oxide; the component B is a zeolite of MOR topology; and a weight ratio of the active ingredients in the component A to the component B is 0.1-20. The reaction process has an extremely high product yield and selectivity, with the selectivity for light olefin reaching 80-90%, wherein ethylene has high space time yield and can reach selectivity of 75-80%. Meanwhile, the selectivity for a methane side product is extremely low (<15%).
Methods of forming and using metal alloy oxidative catalysts
In a first aspect, the present invention is directed to a process for forming a metal alloy catalyst. Another aspect of the present invention is directed to a process for oxidizing a substrate that includes contacting a substrate with an oxidant in the presence of a metal alloy catalyst to form one or more carboxylic acids. Suitable substrates include sugars, polyols, furfural alcohols, and polyhydroxycarboxylic acids. The oxidation process may use the alloy catalyst formed from the process of the first aspect of the invention.
Process for preparing an epoxidation catalyst
A process for preparing a silver-containing catalyst for the selective oxidation of ethylene to ethylene oxide including the steps of: (a) providing a multimodal support, (b) preparing an impregnation solution comprising a silver component, (c) impregnating, at least once, the multimodal support of step (a) with the silver-containing impregnation solution of step (b) to form an impregnated support; (d) subjecting the impregnated multimodal support from step (c) to a removal means, such as a centrifuge, at least once, for a time sufficient to remove impregnated silver impregnation solution from the multimodal support and to control the amount of silver in the pores of the multimodal support by selectively removing impregnated silver impregnation solution from a set of larger pores in the multimodal support; (e) roasting, at least once, the multimodal support after the step (d); (f) optionally, repeating the impregnation step (c), (g) optionally, repeating the centrifugation step (d), and (h) optionally, repeating the calcination step (e).