Patent classifications
B01J35/651
Mesoporous and macroporous nickel-based catalyst having a median macropore diameter of between 50 nm and 200 nm and its use with regard to hydrogenation
A supported catalyst, its method of preparation and use in hydrogenation methods, which catalyst contains an oxide substrate that is for the most part calcined aluminum and an active phase that contains nickel, with the nickel content between 5 and 65% by weight in relation to the total mass of the catalyst, with the active phase not containing a metal from group VIB, the nickel particles having a diameter that is less than or equal to 20 nm, the catalyst having a median mesopore diameter of between 14 nm and 30 nm, a median macropore diameter of between 50 and 200 nm, a mesopore volume that is measured by mercury porosimetry that is greater than or equal to 0.40 mL/g, and a total pore volume that is measured by mercury porosimetry that is greater than or equal to 0.42 mL/g.
VANADIUM-BASED CATALYST AND PREPARATION METHOD THEREFOR
A vanadium-based catalyst comprises an active phase carried on a carrier. The active phase comprises vanadium oxide, potassium sulfate, sodium sulfate, and assistants. The carrier comprises ultra-large-pore silicon dioxide and diatomite, the average pore size of the ultra-large-pore silicon dioxide ranges from 100 nm to 500 nm, and the diatomite is a refined diatomite having a silicon dioxide content of higher than 85% after refinement. The preparation method for the vanadium-based catalyst comprises: 1) mixing potassium vanadium and potassium hydroxide, and allowing a prepared mixed solution and sulfuric acid to carry out a neutralization reaction; and 2) mixing a neutralization reaction product in step 1) with the carrier and sodium sulfate, and carrying out rolling, band extrusion, drying and roasting to prepare the vanadium-based catalyst, assistant compounds being added in step 1) and/or step 2).
Shaped porous carbon products
Shaped porous carbon products and processes for preparing these products are provided. The shaped porous carbon products can be used, for example, as catalyst supports and adsorbents. Catalyst compositions including these shaped porous carbon products, processes of preparing the catalyst compositions, and various processes of using the shaped porous carbon products and catalyst compositions are also provided.
IMMOBILIZING METAL CATALYSTS IN A POROUS SUPPORT VIA ADDITIVE MANUFACTURING AND CHEMICAL VAPOR TRANSFORMATION
A method of immobilizing a metal catalyst in a porous support includes additively forming a precursor structure on a substrate from a metal catalyst and at least one of a metal oxide or a metal cluster compound; exposing the precursor structure to a vapor of an organic linker; and reacting the at least one of the metal oxide or the metal cluster compound in the precursor structure with the organic linker to form a porous support that immobilizes the metal catalyst.
Oligomerization process involving crystalline molecular sieve
A process for oligomerization of olefins includes contacting a feedstock with a zeolite catalyst under conditions of oligomerization at pressure between 8-20 bars and temperature in the range of 60-100 C. to obtain oligomers, wherein, the zeolite catalyst has a pentagonal sheet morphology.
HIGH METALS CONTENT HYDROLYSIS CATALYST FOR USE IN THE CATALYTIC REDUCTION OF SULFUR CONTAINED IN A GAS STREAM, AND A METHOD OF MAKING AND USING SUCH COMPOSITION
Disclosed is a composition useful in the hydrolysis of sulfur compounds that are contained in a gas stream. The composition comprises a calcined co-mulled mixture of psuedoboehmite, a cobalt compound, and a molybdenum compound such that the composition comprises gamma-alumina, at least 7.5 wt. % molybdenum, and at least 2.75 wt. % cobalt. The composition is made by forming into an agglomerate a co-mulled mixture pseudoboehmite, a cobalt component, and a molybdenum component followed by drying and calcining the agglomerate to provide a catalyst composition comprising gamma-alumina, at least 7.5 wt. % molybdenum, and at least 2.75 wt. % cobalt.
Extruded Cu—Al—Mn hydrogenation catalyst
The invention relates to CuAlMn shaped catalyst bodies in extruded form, and to a process for their preparation. The shaped catalyst body is suitable for the hydrogenation of organic compounds containing a carbonyl function, in particular for the hydrogenation of aldehydes, ketones and carboxylic acids and/or their esters. In particular, the shaped catalyst body is suitable for the hydrogenation of fatty acids or their esters, such as fatty acid methyl esters, to form the corresponding alcohols and dicarboxylic acid anhydrides, such as maleic anhydride, or esters of di-acids and di-alcohols, such as butane diol.
Nanoporous cerium oxide with interconnected pores for catalysis and a cost-effective method of preparing thereof
Provided herein are a method of making a nanoporous cerium oxide material which can be used for heterogeneous catalysis. The method may include mixing a cerium nitrate solution and an amine solution to form a mixture and stirring the mixture thus forming a nanoporous cerium oxide precipitate. Further, the molar ratio of cerium nitrate and the amine ranges from 2:1 to 5:1.
PROCESS FOR PREPARING POROUS IRON OXIDE-ZIRCONIA COMPOSITE CATALYST, POROUS IRON OXIDE-ZIRCONIA COMPOSITE CATALYST PREPARED THEREBY, AND METHOD FOR PRODUCING ALCOHOL USING THE CATALYST
The present invention relates to a porous iron oxide-zirconia composite catalyst, a preparation method thereof, and a method for producing alcohol using the same, and the iron oxide-zirconia composite catalyst having a porous structure may produce alcohol at low cost by carrying out an excellent methane reforming reaction even under room temperature and room pressure conditions through an electrochemical reaction.
Method for the hydrotreatment of diesel cuts using a catalyst made from an amorphous mesoporous alumina having high connectivity
There is described a hydroprocessing process of at least one gas oil cut having a weighted mean temperature (TMP) between 240 C. and 350 C. using a catalyst comprising at least one metal of the group VIB and/or at least one metal of the group VIII of the periodic classification and a support comprising an amorphous mesoporous alumina having a connectivity (Z) greater than 2.7, the hydroprocessing process operating at a temperature between 250 C. and 400 C., at a total pressure between 2 MPa and 10 MPa with a ratio of hydrogen volume to volume of hydrocarbon-containing feedstock between 100 and 800 litres per litre and at an Hourly Volume Rate (HVR) which is defined by the ratio of the volume flow rate of liquid hydrocarbon-containing feedstock to volume of catalyst fed into the reactor between 1 and 10 h.sup.1.