623 results about "Ruthenium catalyst" patented technology

The invention relates to novel carbene ligands and their incorporated monomeric and resin/polymer linked ruthenium catalysts, which are recyclable and highly active for olefin metathesis reactions. It is disclosed that significant electronic effect of different substituted 2-alkoxybenzylidene ligands on the catalytic activity and stability of corresponding carbene ruthenium complexes, some of novel ruthenium complexes in the invention can be broadly used as catalysts highly efficient for olefin metathesis reactions, particularly in ring-closing (RCM), ring-opening (ROM), ring-opening metathesis polymerization (ROMP) and cross metathesis (CM) in high yield. The invention also relates to preparation of new ruthenium complexes and the use in metathesis.

The present invention relates to sorbierite cracking process to prepare C2-C4 diatomic alcohol and polyol, and is especially the process of preparing sorbierite with corn material and hydrocracking sorbierite to prepare C2-C4 diatomic alcohol and polyol. The process includes hydrocracking sorbierite to prepare the mixture of C2-C4 diatomic alcohol and polyol at high temperature and high pressure in the presence of cracking sodium hydroxide and nickel/ruthenium catalyst, separation and refining to obtain single product. The production process of the present invention has the advantages of novel production path, unique technological condition, simultaneous production of several kinds of alcohol and high product quality. In addition, using grains, such as corn, as material to replace non-regenerable resource is significant.

Disclosed is a process for preparing a compound of formula I comprising cyclizing a diene compound of formula III in the presence of a ruthenium catalyst in a suitable organic solvent, wherein the process is performed in a gaseous fluid at supercritical or near-supercritical conditions:

The compounds of formula (I) are active agents for the treatment of hepatitis C viral (HCV) infections or are intermediates useful for the preparation of anti-HCV agents.

The present invention relates to a method for deuteration of a compound having an aromatic ring, using an activated catalyst, and the method comprises reacting a compound having an aromatic ring with heavy hydrogen source in the presence of an activated catalyst selected from a platinum catalyst, a rhodium catalyst, a ruthenium catalyst, a nickel catalyst and a cobalt catalyst.

The invention relates to a process for carrying out metathesis reactions, wherein the process is carried out continuously and a ruthenium-containing catalyst is used.

The invention discloses a preparation method for an ordered mesoporous carbon/tungsten carbide composite material and a supported catalyst thereof. In the method, an organic matter and a tungsten salt are separately used as a carbon source and a tungsten source, and the carbon source and the tungsten source are mixed with a surfactant; and a precursor of the ordered mesoporous carbon/tungsten carbide is synthesized by a solvent-evaporation induced self-assembly method, and then the precursor is subject to high-temperature treatment in the inert atmosphere to form the ordered mesoporous carbon/tungsten carbide composite material. The ordered mesoporous carbon/tungsten carbide composite material prepared by the method has the characteristics of high degree of order, narrow aperture distribution, large specific surface area (greater than 500 m<2>/g) and the like. The invention further comprises a supported catalyst prepared by supporting active components on the ordered mesoporous carbon /tungsten carbide composite material which is prepared by the method; and because of the synergistic effect and the structure effect of the ordered mesoporous carbon/tungsten carbide composite material, the catalyst has higher methanol electro-oxidation catalytic activity than a commercial carbon platinum-ruthenium catalyst.

The invention discloses a method for recycling ruthenium in a supported type ruthenium or ruthenium oxide catalyst. The method comprises the following technological steps: (1) placing a supported type ruthenium catalyst or a supported type ruthenium oxide catalyst in an airtight container, heating to 300-500 DEG C, and roasting for 1-2 hours; and feeding nitrogen for protection during roasting process; (2) stopping the feeding of nitrogen stream in the step (1), continuing to heat to 800-1000 DEG C, and roasting for 2-10 hours; and obtaining black solids after cooling; (3) grinding black solids into powder, placing in the airtight container, and heating to 100-300 DEG C; and feeding oxygen/ozone to oxidize solid powder and generate ruthenium tetroxide gas; and (4) feeding the ruthenium tetroxide gas into diluted hydrochloric acid, and restoring the acid combined with the gas into a red and brown ruthenium trichloride solution. According to the device, the step of recycling the catalyst is reduced; not only is the cost reduced during the recycling process of ruthenium catalyst, but also the recycling process is simplified; and economic benefit and the environment benefit are greatly improved.

A recovering process for the activated carbon carried Ru catalyst not containing the compound of alkali metal or alkali-earth metal includes such steps as calcining at 600-1000 deg.C for 2-20 hr to obtain gray mixture, mixing it with KOH and KNO3, holding the temp at 300-950 deg.C for 105 hr, cooling, dissolving in hot water at 50-90 deg.C to obtain K2RuO4 solution, adding sodium hypochlorite and concentrated sulfuric acid, distilling to generate RuO4 gas, absorbing it by strong acid solution, and distilling to obtain Ru salt.

The invention discloses a supported ruthenium catalyst and a preparation method thereof. The preparation method is characterized in that the preparation method comprises the following steps: 1, preprocessing a carrier with a soluble alkaline earth metal salt, wherein the mass of the soluble alkaline earth metal salt accounts for 0.1-20% of the mass of the carrier; and 2, dipping the alkaline earth metal salt processed carrier with a material which comprises a primary active component metallic ruthenium and an assisted catalytic component comprising one or several of Ni, Co, Pd and Pt, wherein the mass of the primary component metallic ruthenium accounts for 0.1-5% of the carrier, and the mass of the secondary component comprising one or several of Ni, Co, Pd and Pt accounts for 0.01-5% of the mass of the carrier. The catalyst of the invention is mainly applied to the selective hydrogenation process of an aromatic ring of an aromatic compound, wherein the aromatic ring of the aromatic compound has at least one alkyl group, one ester group, one hydroxyl group or an amino group and also has at least one C1-8 alkyl group. Compared with catalysts prepared with the prior art, the catalyst of the invention has the advantages of low cost, simple preparation method, high activity, good selectivity, high safety in the operation of the aromatic ring hydrogenation, realization of the operation of the aromatic ring hydrogenation under a low pressure, and good economy.

A process for producing chlorine by oxidizing hydrogen chloride with oxygen. The process uses various supported ruthenium catalysts or a catalyst system containing (A) an active component of a catalyst and (B) a compound having thermal conductivity of a solid phase measured by at least one point within a range from 200 to 500° C. of not less than 4 W/m. ° C.

The invention discloses a method for preparing GAMMA-valerolactone from levulinic acid and formic acid, which is characterized in that the levulinic acid is in situ reduced at 100-200 DEG C in the presence of ruthenium catalyst and formic acid contained in a system as reducer, and distillation is carried out to obtain mixture containing the product GAMMA valerolactone and used catalyst; and mother liquor containing the used catalyst and raw material are mixed to realize circulation of the catalyst, thereby greatly improving environmental friendliness. The method avoids the energy source consumption during valerolactone purification process, avoids hydrogen source acquired from the system exterior, and improves the economy and security of a production system, with the advantages of simple operation process. The formic acid is decomposed to generate large amount of carbon dioxide besides hydrogen, which is convenient for collection and utilization.

The invention discloses a self-humidification membrane electrode for a proton exchange membrane fuel cell and a preparation method thereof. The preparation method comprises the following steps of 1, pre-treating a proton exchange membrane, 2, mixing a carbon-supported platinum or platinum-ruthenium catalyst, a perfluorinated sulfonic acid resin, a hydrophilic organic polymer and an inorganic oxide and in water or a low-boiling point solvent, carrying out ultrasonic treatment to obtain catalyst slurry, and carrying out spray-coating of the catalyst slurry on one side of the proton exchange membrane by an illumination direct-coating technology to obtain an anode catalyst layer, 3, carrying out spray-coating of slurry without the hydrophilic organic polymer and the inorganic oxide on the other side of the proton exchange membrane to obtain a cathode catalyst layer, and 4, carrying out lamination of a gas diffusion layer and the proton exchange membrane of which the two sides are coated with the catalyst layers to obtain the self-humidification membrane electrode. The anode catalyst layer contains the hydrophilic organic polymer and the inorganic oxide so that the self-humidification membrane electrode has excellent self-humidification performances at a high cell temperature and low humidity.

The invention discloses a method for synthesizing cyclohexylamine with aniline by means of gas-phase catalytic hydrogenation, which includes the steps: 1) mixing fresh hydrogen with circulating hydrogen; 2) mixing mixed hydrogen with the aniline according to the molar ratio of 15:1-19:1 in an aniline evaporator to enable vaporization of the aniline; 3) carrying out a hydrogenation reaction of vaporized mixed gas in a fixed bed hydrogenation reactor prefilled with cobalt-ruthenium catalyst or nickel-ruthenium catalyst at the reaction temperature of 165-179 DEG C and under the reaction pressureof 0.2-0.3MPa; and 4) materials which are subjected to the hydrogenation reaction enter a separator by means of heat exchange, condensation and cooling, performing gas separation to obtain crude cyclohexylamine, and then rectifying so that a cyclohexylamine product is prepared. By the aid of the method, production cost is effectively reduced, product yield is increased, and the service life of the catalyst is prolonged.

The present invention relates to novel Ruthenium catalysts and related borohydride complexes, and the use of such catalysts, inter alia, for (1) hydrogenation of amides (including polyamides) to alcohols and amines; (2) preparing amides from alcohols with amines (including the preparation of polyamides (e.g., polypeptides) by reacting dialcohols and diamines and/or by polymerization of amino alcohols); (3) hydrogenation of esters to alcohols (including hydrogenation of cyclic esters (lactones) or cyclic di-esters (di-lactones) or polyesters); (4) hydrogenation of organic carbonates (including polycarbonates) to alcohols and hydrogenation of carbamates (including polycarbamates) or urea derivatives to alcohols and amines; (5) dehydrogenative coupling of alcohols to esters; (6) hydrogenation of secondary alcohols to ketones; (7) amidation of esters (i.e., synthesis of amides from esters and amines); (8) acylation of alcohols using esters; (9) coupling of alcohols with water to form carboxylic acids; and (10) dehydrogenation of beta-amino alcohols to form pyrazines. The present invention further relates to the novel uses of certain pyridine Ruthenium catalysts.

Chiral ruthenium catalysts comprising salen and alkenyl ligands are provided for stereoselective cyclopropanation, and methods of cyclopropanation are provided. The chiral ruthenium catalyst is prepared in situ by combining an alkenyl ligand, a deprotonated chiral salen ligand, and a ruthenium (II) metal. A preferred catalyst is prepared in situ by combining 2,3-dihydro-4-venylbenzofuran, deprotonated 1,2-cyclohexanediamino-N,N′-bis(3,5-di-t-butyl-salicylidene) and RuCl₂(p-cymene)]₂.

The invention provides a ruthenium catalyst for ammonia synthesis with high activity which has composite oxide as a carrier, and a preparation method thereof. The ruthenium catalysts for ammonia synthesis comprises composite oxide as the carrier, metal Ru as an active component, wherein the capacity is 1-12 wt.% of the active carbon weight calculated based on Ru. The composite oxide is formed by magnesium and one or two or more than two nonferrous metal of: 1) alkaline earth but not magnesium; 2) alkali metals; 3) rare earth metal, wherein the ratio of magnesium and the nonferrous metal based on the amount of substance is 0.2-25:1. The catalyst of the invention has higher catalytic activity and better application prospects compared with the existing ruthenium catalyst for ammonia synthesis which has oxide as a carrier.