B01J37/105

METHODS FOR PREPARING CATALYTIC SYSTEMS
20210170368 · 2021-06-10 ·

Methods for preparing catalytic systems include passivating a gamma-phase alumina support body to yield a theta-phase alumina support body and applying catalytic metal to passivated theta-phase alumina support body. Passivating can include heating, optionally in the presence of steam. The gamma-phase alumina can be lanthanum-doped gamma-phase alumina and can be about 0.1-55 wt. % lanthanum. The catalytic metal can include rhodium, copper, or nickel. The catalytic metal can be rhodium or nickel, and the catalytic metal can be applied to the passivated theta-phase alumina support body at a loading of about 0.1-10 wt. %. The catalytic metal can be copper, and the catalytic metal can be applied to the passivated theta-phase alumina support body at a loading of about 0.1-30 wt. %. The gamma-phase alumina support body can be at least about 90 wt. % gamma-phase alumina. The passivated theta-phase alumina support body can be at least about 80 wt. % theta-phase alumina.

Process for preparing a catalyst and use thereof

The present invention provides a process for preparing a catalyst, wherein said process comprises:—(i) preparing a mixture of one or more aromatic alcohol monomers and/or non-aromatic monomers, solvent, polymerization catalyst, crosslinking agent, suspension stabilizing agent and one or more metal salts, under conditions sufficient to produce polymeric beads doped with one or more metals or salts thereof; (ii) carbonizing, activating and then reducing the polymeric beads produced in step (i) to produce metal nanoparticles-doped porous carbon beads; (iii) subjecting the metal nanoparticles-doped porous carbon beads produced in step (ii) to chemical vapour deposition in the presence of a carbon source to produce metal nanoparticles-doped porous carbon beads comprising carbon nanofibers; and (iv) doping the metal nanoparticles-doped porous carbon beads comprising carbon nanofibers produced in step (iii) with an oxidant; catalyst prepared by said process; and a process for treating waste water from an industrial process for producing propylene oxide, which process comprises subjecting the waste water to a catalytic wet oxidation treatment in the presence of said catalyst.

METHODS OF PRODUCING ISOMERIZATION CATALYSTS

Methods of producing an isomerization catalyst include preparing a catalyst precursor solution, hydrothermally treating the catalyst precursor solution to produce a magnesium oxide precipitant, and calcining the magnesium oxide precipitant to produce the isomerization catalyst. The catalyst precursor solution includes at least a magnesium precursor, a hydrolyzing agent, and cetrimonium bromide. Methods of producing 1-butene from a 2-butene-containing feedstock with the isomerization catalyst are also disclosed.

ZrCe-SBA-15-NiMo HYDRODESULFURIZATION CATALYST

A robust catalyst useful for hydrodesulfurization (HDS) of sulfur-containing hydrocarbons such as sulfur-containing diesel fuel. The catalyst contains a modified mesoporous silica, such as SBA-15, Zr atoms, Ni, Mo, Ce atoms. A method for removing sulfur from a hydrocarbon, such as diesel fuel or a refinery feedstock using the catalyst. A one-pot method for making the catalyst.

PHOSPHORUS-DOPED TUBULAR CARBON NITRIDE MICRO-NANO MATERIAL AND APPLICATION THEREOF IN CATALYTIC TREATMENT OF EXHAUST GAS
20200282384 · 2020-09-10 ·

The invention discloses a phosphorus-doped tubular carbon nitride micro-nano material and application thereof in waste gas treatment. Melamine is partially hydrolyzed into cyanuric acid through a phosphorous acid-assisted hydrothermal method to form a melamine-cyanuric acid super molecular precursor; the center of the precursor starts to be pyrolyzed under heating calcination, and thus phosphorus-doped tubular carbon nitride is obtained; the phosphorus-doped tubular carbon nitride and sodium borohydride are mixed and subjected to low-temperature calcination in an inert gas atmosphere, and defect-modified phosphorus-doped tubular carbon nitride is obtained. The defect-modified phosphorus-doped tubular carbon nitride micro-nano material has a good photocatalytic effect on catalytic degradation of waste gas; besides, the production raw materials are abundant and easy to obtain, and the phosphorus-doped tubular carbon nitride micro-nano material is good in stability and recyclable and has application prospects in waste gas treatment.

PROCESS FOR PREPARING A CATALYST AND USE THEREOF
20200171477 · 2020-06-04 ·

The present invention provides a process for preparing a catalyst, wherein said process comprises:(i) preparing a mixture of one or more aromatic alcohol monomers and/or non-aromatic monomers, solvent, polymerization catalyst, crosslinking agent, suspension stabilizing agent and one or more metal salts, under conditions sufficient to produce polymeric beads doped with one or more metals or salts thereof; (ii) carbonizing, activating and then reducing the polymeric beads produced in step (i) to produce metal nanoparticles-doped porous carbon beads; (iii) subjecting the metal nanoparticles-doped porous carbon beads produced in step (ii) to chemical vapour deposition in the presence of a carbon source to produce metal nanoparticles-doped porous carbon beads comprising carbon nanofibers; and (iv) doping the metal nanoparticles-doped porous carbon beads comprising carbon nanofibers produced in step (iii) with an oxidant; catalyst prepared by said process; and a process for treating waste water from an industrial process for producing propylene oxide, which process comprises subjecting the waste water to a catalytic wet oxidation treatment in the presence of said catalyst.

Stepwise solidus synthesis method for a micro-mesoporous calcium aluminate catalyst

The present disclosure relates to the technical field of fine chemical engineering, and particularly discloses a stepwise solidus synthesis method for a micro-mesoporous calcium aluminate catalyst, comprising: mixing a calcium oxide-based powder with an alumina-based powder and an adhesion pore-enlarging agent; pelleting and molding the mixture; pyrolyzing and coking the pelleted and molded product in a rotary kiln reactor under the conditions including an outlet reaction temperature of 300 C.500 C. and a residence time of 0.23.5 h; and subsequently carrying out a solidus reaction in an internal heating rotary kiln reactor under the conditions including an outlet reaction temperature of 900 C.1,500 C. and a residence time of 0.15 h to produce calcium aluminate; decomposing and gasifying the pyrolyzed char in the calcium aluminate to promote the formation of pores, thereby producing micro-mesoporous calcium aluminate catalyst; wherein the weight ratio between the calcium oxide-based powder and the alumina-based powder is within a range of 12:(215), the added amount of the adhesion pore-enlarging agent accounts for 0.115% by weight of a total amount of the calcium oxide-based powder and alumina-based powder; wherein the weight of the calcium oxide-based powder is calculated based on calcium oxide, and the weight of the alumina-based powder is calculated based on alumina. The calcium aluminate catalyst prepared with the method provided by the present disclosure has advantages of large specific surface area, low density and high strength.

STEPWISE SOLIDUS SYNTHESIS METHOD FOR A MICRO-MESOPOROUS CALCIUM ALUMINATE CATALYST

The present disclosure relates to the technical field of fine chemical engineering, and particularly discloses a stepwise solidus synthesis method for a micro-mesoporous calcium aluminate catalyst, comprising: mixing a calcium oxide-based powder with an alumina-based powder and an adhesion pore-enlarging agent; pelleting and molding the mixture; pyrolyzing and coking the pelleted and molded product in a rotary kiln reactor under the conditions including an outlet reaction temperature of 300 C.500 C. and a residence time of 0.23.5 h; and subsequently carrying out a solidus reaction in an internal heating rotary kiln reactor under the conditions including an outlet reaction temperature of 900 C.1,500 C. and a residence time of 0.15 h to produce calcium aluminate; decomposing and gasifying the pyrolyzed char in the calcium aluminate to promote the formation of pores, thereby producing micro-mesoporous calcium aluminate catalyst; wherein the weight ratio between the calcium oxide-based powder and the alumina-based powder is within a range of 12:(215), the added amount of the adhesion pore-enlarging agent accounts for 0.115% by weight of a total amount of the calcium oxide-based powder and alumina-based powder; wherein the weight of the calcium oxide-based powder is calculated based on calcium oxide, and the weight of the alumina-based powder is calculated based on alumina. The calcium aluminate catalyst prepared with the method provided by the present disclosure has advantages of large specific surface area, low density and high strength.

STRUCTURED CATALYST FOR AROMATIC HYDROCARBON PRODUCTION, AROMATIC HYDROCARBON PRODUCING DEVICE INCLUDING THE STRUCTURED CATALYST FOR AROMATIC HYDROCARBON PRODUCTION, METHOD FOR PRODUCING STRUCTURED CATALYST FOR AROMATIC HYDROCARBON PRODUCTION, AND METHOD FOR PRODUCING AROMATIC HYDROCARBON

Provided are a structured catalyst for aromatic hydrocarbon production and an aromatic hydrocarbon producing device including a structured catalyst for aromatic hydrocarbon production, in which a reduction in catalytic activity is suppressed and an aromatic hydrocarbon can be efficiently produced. A structured catalyst for aromatic hydrocarbon production, including:

a support of a porous framework composed of a zeolite-type compound; and

at least one catalytic substance present in the support,

in which the support has channels communicating with each other, and

the catalytic substance is made of metal nanoparticles and is present at least in the channels of the support.

FUNCTIONAL STRUCTURAL BODY AND METHOD FOR MAKING FUNCTIONAL STRUCTURAL BODY

A functional structural body includes a skeletal body of a porous structure composed of a zeolite-type compound, and at least one type of metallic nanoparticles present in the skeletal body, the skeletal body having channels connecting with each other, the metallic nanoparticles being present at least in the channels of the skeletal body.