B01J21/10

Adsorbent, Liquid Phase Hydrogenation Catalyst Composition, Catalyst Bed and Use Thereof

An adsorbent is in a liquid-phase hydrogenation catalyst composition. A catalyst bed containing the liquid-phase hydrogenation catalyst composition may be applicable in adsorption technology or oil liquid-phase hydrogenation technology. The adsorbent contains a porous material and a hydrogenation active metal supported on the porous material. The adsorbent has an average pore diameter of 2-15 nm, a specific surface area of 200-500 m.sup.2/g, and the hydrogenation active metal is present in an amount, calculated as metal oxide, of 2.5 wt % or less, based on the total weight of the adsorbent. The adsorbent has a high hydrogen sulfide adsorption efficiency for a long period of time, and can effectively prolong the protection period for the hydrodesulfurization catalyst.

Adsorbent, Liquid Phase Hydrogenation Catalyst Composition, Catalyst Bed and Use Thereof

An adsorbent is in a liquid-phase hydrogenation catalyst composition. A catalyst bed containing the liquid-phase hydrogenation catalyst composition may be applicable in adsorption technology or oil liquid-phase hydrogenation technology. The adsorbent contains a porous material and a hydrogenation active metal supported on the porous material. The adsorbent has an average pore diameter of 2-15 nm, a specific surface area of 200-500 m.sup.2/g, and the hydrogenation active metal is present in an amount, calculated as metal oxide, of 2.5 wt % or less, based on the total weight of the adsorbent. The adsorbent has a high hydrogen sulfide adsorption efficiency for a long period of time, and can effectively prolong the protection period for the hydrodesulfurization catalyst.

Catalyst for producing light olefins from C4-C7 hydrocarbons

The present invention relates to a catalyst for producing light olefins from C4-C7 hydrocarbons from catalytic cracking reaction and the production process of light olefins from said catalyst, wherein said catalyst has core-shell structure comprising a zeolite core with mole ratio of silicon to aluminium (Si/Al) between 2 to 250 and layered double hydroxide shell (LDH). The catalyst according to the invention provides high percent conversion of substrate to products and high selectivity to light olefins product.

Catalyst for producing light olefins from C4-C7 hydrocarbons

The present invention relates to a catalyst for producing light olefins from C4-C7 hydrocarbons from catalytic cracking reaction and the production process of light olefins from said catalyst, wherein said catalyst has core-shell structure comprising a zeolite core with mole ratio of silicon to aluminium (Si/Al) between 2 to 250 and layered double hydroxide shell (LDH). The catalyst according to the invention provides high percent conversion of substrate to products and high selectivity to light olefins product.

ELECTRICALLY HEATED EXHAUST GAS PURIFICATION CATALYST
20230338929 · 2023-10-26 ·

An object of the present invention is to provide an electrically heated exhaust gas purification catalyst that is less likely to cause the deterioration of the exhaust gas purification performance, and, in order to achieve this object, the present invention provides an electrically heated exhaust gas purification catalyst (1) including: a substrate (10); at least one pair of electrodes (20a, 20b) provided on the substrate (10); an undercoat layer (30) provided on the substrate (10), the undercoat layer (30) containing an aluminum oxide as a main component; and a catalyst layer (40) provided on the undercoat layer (30), the catalyst layer (40) containing a noble metal element, wherein the undercoat layer (30) contains a Group 2 element.

ELECTRICALLY HEATED EXHAUST GAS PURIFICATION CATALYST
20230338929 · 2023-10-26 ·

An object of the present invention is to provide an electrically heated exhaust gas purification catalyst that is less likely to cause the deterioration of the exhaust gas purification performance, and, in order to achieve this object, the present invention provides an electrically heated exhaust gas purification catalyst (1) including: a substrate (10); at least one pair of electrodes (20a, 20b) provided on the substrate (10); an undercoat layer (30) provided on the substrate (10), the undercoat layer (30) containing an aluminum oxide as a main component; and a catalyst layer (40) provided on the undercoat layer (30), the catalyst layer (40) containing a noble metal element, wherein the undercoat layer (30) contains a Group 2 element.

Exhaust gas purification system

An exhaust gas purification system of the present disclosure includes a first exhaust gas purification device that purifies exhaust gas discharged from an internal combustion engine and a second exhaust gas purification device that additionally purifies the exhaust gas purified by the first exhaust gas purification device, wherein the exhaust gas is exhaust gas with a gaseous composition in which an amount of reducing agents is in excess compared to a stoichiometric gaseous composition and a gaseous composition in which an amount of oxidants is in excess compared to the stoichiometric gaseous composition are alternately switched between, the first exhaust gas purification device includes a three-way catalyst, and the second exhaust gas purification device includes an exhaust gas purification catalyst containing spinel-type MgAl.sub.xFe.sub.2.00−xO.sub.4.00 supporting particles on which Rh is supported, where 0.00<×≤1.50.

PROCESS FOR PREPARING SOLID CATALYST COMPONENTS FOR OLEFIN POLYMERIZATION

A process of preparing a solid catalyst component for the production of polypropylene includes a) dissolving a halide-containing magnesium compound in a mixture, the mixture including an epoxy compound, an organic phosphorus compound, and a hydrocarbon solvent to form a homogenous solution; b) treating the homogenous solution with an organosilicon compound during or after the dissolving step; c) treating the homogenous solution with a first titanium compound in the presence of a first non-phthalate electron donor, and an organosilicon compound, to form a solid precipitate; and d) treating the solid precipitate with a second titanium compound in the presence of a second non-phthalate electron donor to form the solid catalyst component, where the process is free of carboxylic acids and anhydrides.

Supported catalyst and method for preparing light olefin using direct conversion of syngas

A supported catalyst for preparing light olefin using direct conversion of syngas is a composite catalyst and formed by compounding component I and component II in a mechanical mixing mode. The active ingredient of component I is a metal oxide; and the component II is a supported zeolite. A carrier is one or more than one of hierarchical pores Al.sub.2O.sub.3, SiO.sub.2, TiO.sub.2, ZrO.sub.2, CeO.sub.2, MgO and Ga.sub.2O.sub.3; the zeolite is one or more than one of CHA and AEI structures; and the load of the zeolite is 4%-45% wt. A weight ratio of the active ingredients in the component I to the component II is 0.1-20. The reaction process has an extremely high light olefin selectivity; the sum of the selectivity of the light olefin comprising ethylene, propylene and butylene can reach 50-90%, while the selectivity of a methane side product is less than 7%.

Supported catalyst and method for preparing light olefin using direct conversion of syngas

A supported catalyst for preparing light olefin using direct conversion of syngas is a composite catalyst and formed by compounding component I and component II in a mechanical mixing mode. The active ingredient of component I is a metal oxide; and the component II is a supported zeolite. A carrier is one or more than one of hierarchical pores Al.sub.2O.sub.3, SiO.sub.2, TiO.sub.2, ZrO.sub.2, CeO.sub.2, MgO and Ga.sub.2O.sub.3; the zeolite is one or more than one of CHA and AEI structures; and the load of the zeolite is 4%-45% wt. A weight ratio of the active ingredients in the component I to the component II is 0.1-20. The reaction process has an extremely high light olefin selectivity; the sum of the selectivity of the light olefin comprising ethylene, propylene and butylene can reach 50-90%, while the selectivity of a methane side product is less than 7%.