B01J38/72

Systems and methods for segregating into dual waste streams oxidizable catalyst material from inert support media
12214342 · 2025-02-04 · ·

A method for disposing of a mixture of oxidizable catalyst material and inert support media. The method comprises introducing inert gas into an enclosure. The enclosure contains a plurality of stacked screens, the stacked screens have openings that decrease in size from a top of the stack to a bottom of the stack. The method also comprises introducing the mixture to an uppermost one of the plurality of stacked screens; moving the plurality of stacked screens to cause the oxidizable catalyst material to separate from and migrate to a location beneath the inert support media; conveying the separated inert support media to a location outside the enclosure for disposal as non-hazardous waste; and conveying the separated oxidizable catalyst material to a location outside the enclosure for at least one of reclamation, or thermal destruction.

CATALYST AND PROCESS FOR CONVERSION OF VACUUM RESID TO MIDDLE DISTILLATES

This invention relates to a process for hydro cracking of heavy oils. More particularly, this invention relates to a catalytic process for converting heavy oils, such as vacuum gas oil (VGO) and VGO containing a high proportion of vacuum resid (VR) to middle distillate products.

SEPARATION OF CATALYST AND INERT HEAT PARTICLE AFTER AROMATIZATION OF A METHANE CONTAINING GAS STREAM

Implementations of the disclosed subject matter provide a process for the aromatization of a methane-containing gas stream may include contacting the methane-containing gas stream in a reaction zone comprising an aromatization catalyst particulate and an inert heat carrier particulate under methane-containing gas aromatization reaction conditions to produce a product stream comprising aromatics in the reaction zone. The inert heat carrier particulate may be separated from the aromatization catalyst particulate in a separation zone under separation conditions. The aromatization catalyst particulate may have a first minimum fluidization velocity and the inert heat carrier particulate may have a second minimum fluidization velocity which may be greater than the first minimum fluidization velocity. The ratio of the second minimum fluidization velocity to the first minimum fluidization velocity may be less than 200 and may be more than 15.

SEPARATION OF CATALYST AND HYDROGEN ACCEPTOR AFTER AROMATIZATION OF A METHANE CONTAINING GAS STREAM

Implementations of the disclosed subject matter provide a process for the aromatization of a methane-containing gas stream including contacting the methane-containing gas stream in a reaction zone comprising an aromatization catalyst particulate and a hydrogen acceptor particulate under methane-containing gas aromatization reaction conditions to produce reaction products comprising aromatics and gaseous hydrogen. At least a portion of the gaseous hydrogen produced is bound by the hydrogen acceptor particulate in the reaction zone and removed from the reaction products in the reaction zone. Further, the hydrogen acceptor particulate may be separated from the aromatization catalyst particulate in a separation zone under separation conditions.

Method for regenerating SCR denitration catalyst assisted by microwaves and device therefor

Disclosed is a method for regenerating a SCR denitration catalyst assisted by microwaves. The method comprises: (1) a poisoned SCR denitration catalyst is immersed in deionized water, and the SCR denitration catalyst is cleaned by a bubbling method; (2) the SCR denitration catalyst is transferred to a container containing a pore-expanding solution for a soaking treatment; (3) the SCR denitration catalyst is transferred to a microwave device and treated for 1-10 minutes; (4) the SCR denitration catalyst is transferred to a container with an activating liquid and impregnated for 1-4 hours; (5) the SCR denitration catalyst is dried with microwaves for 1-20 minutes; and (6) the SCR denitration catalyst is calcined under conditions of 500-600 C. for 4-7 hours. The present invention has readily available raw materials, is simple and energy-saving in device and process, and is suitable for industrial scale regeneration. The catalyst treated by the method of the present invention has the advantages of loose pore channels, obviously optimized pore structures, significantly improved catalyst surface conditions, high activity, and good economic benefits.

Alternating fixed and fluidized bed reactor systems and processes

The present disclosure refers to systems and methods for producing hydrogen among other products. In some embodiments the methods comprise sequentially conducting a cracking step in a fixed bed mode and conducting a flowing step in a fluidized bed mode. Such sequential processes may result in a number of advantages including, for example, regenerating the catalyst during the fluidized bed mode in a manner such that beneficial heat is generated for use in the endothermic cracking step.

Alternating fixed and fluidized bed reactor systems and processes

The present disclosure refers to systems and methods for producing hydrogen among other products. In some embodiments the methods comprise sequentially conducting a cracking step in a fixed bed mode and conducting a flowing step in a fluidized bed mode. Such sequential processes may result in a number of advantages including, for example, regenerating the catalyst during the fluidized bed mode in a manner such that beneficial heat is generated for use in the endothermic cracking step.

SYSTEMS AND METHODS FOR SEGREGATING INTO DUAL WASTE STREAMS OXIDIZABLE CATALYST MATERIAL FROM INERT SUPPORT MEDIA
20250269365 · 2025-08-28 · ·

A method for disposing of a mixture of oxidizable catalyst material and inert support media. The method comprises introducing inert gas into an enclosure. The enclosure contains a plurality of stacked screens, the stacked screens have openings that decrease in size from a top of the stack to a bottom of the stack. The method also comprises introducing the mixture to an uppermost one of the plurality of stacked screens; moving the plurality of stacked screens to cause the oxidizable catalyst material to separate from and migrate to a location beneath the inert support media; conveying the separated inert support media to a location outside the enclosure for disposal as non-hazardous waste; and conveying the separated oxidizable catalyst material to a location outside the enclosure for at least one of reclamation, or thermal destruction.

SYSTEMS AND METHODS FOR SEGREGATING INTO DUAL WASTE STREAMS OXIDIZABLE CATALYST MATERIAL FROM INERT SUPPORT MEDIA
20250269365 · 2025-08-28 · ·

A method for disposing of a mixture of oxidizable catalyst material and inert support media. The method comprises introducing inert gas into an enclosure. The enclosure contains a plurality of stacked screens, the stacked screens have openings that decrease in size from a top of the stack to a bottom of the stack. The method also comprises introducing the mixture to an uppermost one of the plurality of stacked screens; moving the plurality of stacked screens to cause the oxidizable catalyst material to separate from and migrate to a location beneath the inert support media; conveying the separated inert support media to a location outside the enclosure for disposal as non-hazardous waste; and conveying the separated oxidizable catalyst material to a location outside the enclosure for at least one of reclamation, or thermal destruction.

RECYCLING OF POLYMER MEMBRANES COMPRISING METAL-CONTAINING CATALYST MATERIAL
20250369141 · 2025-12-04 ·

The invention relates to a method for recycling polymer membranes comprising metal-containing catalyst material. The method comprises the following steps adding water without adding organic solvents to a polymer membrane comprising a metal-containing catalyst material to form a polymer membrane/water mixture, simultaneously increasing the pressure and the temperature of the polymer membrane/water mixture to a pressure between 20 bar and 40 bar and a temperature between 200 C. and 250 C., a liquid phase and a solid phase being formed, and separating the liquid phase and the solid phase.