B01J35/69

CATALYST AND METHOD FOR REMOVING NOX FROM COMBUSTION EXHAUST GAS

Provided is a catalyst for removing NOx from a combustion exhaust gas, in particular, a low-NOx combustion exhaust gas, wherein the catalyst has a ratio of a pore volume in a range of not less than 500 ? and not more than 3000 ? in a pore diameter relative to a total pore volume of not less than 15% and not more than 40% and preferably a ratio of a pore volume in a range of not less than 1000 ? in the pore diameter relative to the total pore volume of not less than 10% and not more than 45% in a pore volume distribution in a range of not more than 10.sup.5 ? in the pore diameter, and where SILICA is unlikely to be deposited and even when the amount of SILICA deposited is increased, denitration performance is hardly lowered.

Hydrogenation catalyst and process for production thereof by the use of uncalcined starting material

The invention relates to a process for preparing a shaped CuAl catalyst body for the hydrogenation of organic compounds containing a carbonyl function. More particularly, the shaped catalyst body is suitable for the hydrogenation of aldehydes, ketones and of carboxylic acids or esters thereof, specifically of fatty acids or esters thereof, such as fatty acid methyl esters, to the corresponding alcohols such as butanediol. The present invention further relates to CuAl catalysts obtainable by the preparation process.

EXHAUST GAS PURIFICATION FILTER
20190299139 · 2019-10-03 · ·

An exhaust gas purification filter that suppresses an increase in pressure loss associated with the formation of a catalyst layer and is excellent in PM burning quality. The exhaust gas purification filter includes a base and a catalyst layer provided on the base. The catalyst layer contains a carrier and a metal catalyst. Large pores having a circle equivalent diameter greater than 5 ?m occupy, when an area of the catalyst layer is 100% in an electron microscope observation image of a cross section of the catalyst layer, 45% or more of the area.

Methods for synthesizing hierarchical zeolites for catalytic cracking

Provided here are zirconium-substituted hierarchical zeolite compositions and methods of preparing such catalytic compositions. One such method involves subjecting the zirconium-substituted zeolite to a framework modification process using a single template to produce a framework-modified zeolite, followed by subjecting the framework-modified zeolite to an ion exchange process to produce a hierarchical zeolite composition. Also provided are methods of catalytic cracking of hydrocarbon feedstocks using these zirconium-substituted hierarchical zeolite compositions.

Alloyed zeolite catalyst component, method for making and catalytic application thereof

The presently disclosed and claimed inventive concept(s) generally relates to a solid catalyst component comprising a zeolite with a modifier and at least one Group VIII meal alloyed with at least one transition metal. The presently disclosed and claimed inventive concept(s) further relates to a method of making the solid catalyst component and a process of converting mixed waste plastics into low molecular weight organic compounds using the solid catalyst component.

Process for preparing a structurally selective oligomerization catalyst of prolonged stability by precipitation

A process for preparing an oligomerization catalyst is based on using nickel aluminosilicate that has high activity and selectivity coupled with adequate service life in the heterogeneously catalysed oligomerization of C3 to C6 olefins or olefin-containing feed mixtures based thereon.

Zeolites, the production thereof, and their uses for upgrading heavy oils

According to one or more embodiments disclosed herein, a mesoporous zeolite may be made by a method comprising contacting an initial zeolite material with ammonium hexafluorosilicate to modify the framework of the initial zeolite material, and forming mesopores in the framework-modified zeolite material. The contacting may form a framework-modified zeolite material. The mesoporous zeolites may be incorporated into catalysts.

PROCESS FOR PREPARING A MESOPORIZED CATALYST, CATALYST THUS OBTAINED AND USE THEREOF IN A CATALYTIC PROCESS
20190262810 · 2019-08-29 · ·

A hydroconversion catalyst obtained by the process described, comprising a mesoporized zeolite with healed zeolitic structure, containing at least one network of micropores and at least one network of mesopores, having an atomic Si/Al ratio within the zeolite framework of greater than or equal to 2.3 and showing reduced amount of extra-framework aluminium with regard to that of a mesoporized zeolite with no healed zeolitic structure.

Methods of producing hierarchical beta zeolites with tunable mesoporosity through pore directing agent assisted base leaching
10391480 · 2019-08-27 · ·

Methods for producing mesoporous beta zeolites from parent beta zeolites having a Si/Al molar ratio of at least 10 comprise selecting a target average mesoporous size between 2 nm and 8 nm for the parent beta zeolites, selecting a pore directing agent (PDA) based on the target average mesopore size, where a non-ionic surfactant, a small cationic surfactant has a molecular weight of greater than 100 grams/mole, or both may be selected as the PDA when the target average mesopore size is at least 5 nm, and a large cationic surfactant having a molecular weight of less than 100 grams/mole may be selected as the PDA when the target average mesopore size is less than 5 nm. The method further comprises adding the selected PDA to an alkaline solution to form a PDA-base mixture, and adding the parent beta zeolites to the PDA-base mixture to produce the mesoporous beta zeolites.

Composition comprising cerium oxide and zirconium oxide having a specific porosity, preparation method thereof and use of same in catalysis
10384954 · 2019-08-20 · ·

A composition including cerium and zirconium oxides, including at least 30 wt.-% cerium oxide is desired. Following calcination at a temperature of 900 DEG C. for 4 hours, the composition has two populations of pores, the diameters of the first population being centered around a value of between 5 nm and 15 nm for a composition including 30% to 65% cerium oxide or between 10 nm and 20 nm for more than 65% cerium oxide and the diameter of the second population being centered around a value of between 45 nm and 65 nm for 30% to 65% cerium oxide or between 60 nm and 100 nm for more than 65% cerium oxide.