B01J37/0213

CATALYST PREPARATION METHOD

A method is described for preparing an eggshell catalyst comprising the steps of: (i) preparing a calcined shaped alkaline earth metal aluminate catalyst support, (ii) treating the calcined shaped alkaline earth metal aluminate support with a gas containing water vapour to form a hydrated support, (iii) with or without an intervening drying step, impregnating the hydrated support with an acidic solution containing one or more catalytic metal compounds and drying the impregnated support, (iv) calcining the dried impregnated support, to form a calcined catalyst having a catalytic metal oxide concentrated at the surface of the support and (v) optionally repeating steps (ii), (iii) and (iv).

Photocatalytic composite material and preparation method and application thereof

The present invention provides a preparation method of a photocatalytic composite material, and relates to the field of catalyst technologies. The preparation method provided in the present invention includes the following steps: (1) subjecting plant leaves to soaking pretreatment to obtain template biomass; (2) mixing a molybdenum source-sulfur source aqueous solution with the template biomass obtained in step (1) and conducting impregnation to obtain a composite material precursor; and (3) calcining the composite material precursor obtained in step (2) to obtain the photocatalytic composite material. The photocatalytic composite material in the present invention includes acicular molybdenum sulfide and biomass carbon, the acicular molybdenum sulfide is loaded to a surface of the flake carbon, the mass content of the biomass carbon is 70% to 90%, and the mass content of the molybdenum sulfide is 10% to 30%. Performance of photocatalytic hydrogen production of the photocatalytic composite material in the present invention is better than that of a pure molybdenum sulfide material and has excellent photocorrosion resistance, and hydrogen production efficiency is reduced by only approximately 10% after three cycles.

DOPED TIN OXIDE PARTICLES AND DOPED TIN OXIDE SHELLS FOR CORE-SHELL PARTICLES

The present disclosure relates to a strategy to synthesize antimony- and zinc-doped tin oxide particles with tunable band gap characteristics. The methods yield stable and monodispersed particles with great control on uniformity of shape and size. The methods produce undoped and antimony and zinc-doped tin oxide stand-alone and core-shell particles, both nanoparticles and microparticles, as well as antimony and zinc-doped tin oxide shells for coating particles, including plasmonic core particles.

CO-DEFLAGRATION SYNTHESIS OF METALLIC, CERAMIC, AND MIXED CERAMIC-METALLIC PARTICLES

A co-deflagration process for the preparation of metallic, ceramic, or mixed ceramic-metallic particles optionally impregnated within or attached to a metallic, ceramic, or mixed ceramic-metallic support material includes mixing at least two components. Each of the components can be any of a nitrogen-rich ligand or a salt thereof, a complex or coordination polymer of the nitrogen-rich ligand or salt thereof with one of the at least one metal, and a cluster of the at least one metal, and optionally an organic or inorganic oxidant, gas generator, pyrotechnic, propellant, and/or explosive.

HIGH ACTIVITY SECOND STAGE NAPHTHA HYDROCRACKING CATALYST

Provided is a novel catalyst for use in the second stage of a two-stage hydrocracking process. The present process comprises hydrocracking a hydrocarbon feed in a first stage. The catalyst in the first stage is a conventional hydrocracking catalyst. The product from the first stage can then be transferred to a second hydrocracking stage. The catalyst used in the second stage of the present hydrocracking process comprises a base impregnated with metals from Group 6 and Groups 8 through 10 of the Periodic Table, and an organic acid. The base of the catalyst used in the present second hydrocracking stage comprises alumina, an amorphous silica-alumina (ASA) material, and a USY zeolite. Improved naphtha production is achieved.

Monolithic catalyst used for carbon dioxide hydrogenation reaction and method for preparing same

A monolithic catalyst used for a carbon dioxide hydrogenation reaction and a method for preparing the same. The catalyst comprises a carrier, a coating, and active components. The carrier is a honeycomb ceramic. The coating and the active components are separately applied to honeycomb ceramic hole walls from inside to outside. Moreover, each of the honeycomb ceramic holes is divided into an upper segment and a lower segment, and different active components are separately loaded on the two segments. The method for preparing the monolithic catalyst comprises first applying a coating to a honeycomb ceramic by means of impregnation to obtain a coating-containing carrier, and then applying active components to an upper segment and a lower segment of the coating-containing carrier successively by means of impregnation to obtain the monolithic catalyst.

OXIDES OF SULFUR AND THEIR USE AS OXYGEN TRANSFER REAGENTS
20230271170 · 2023-08-31 · ·

An oxide of sulfur oxygen transfer reagent is provided. A method of producing olefins from hydrocarbons with a concomitant production of water (oxidative dehydrogenation), using the oxide of sulfur oxygen transfer reagent is also provided. The sulfur oxygen transfer reagent can be used as an oxygen transfer reagent, and therefore acts as a non-metal carrier, for oxygen in a redox looping reactor for an oxidative dehydrogenation process such as the conversion of ethane to ethylene. The reduced forms of oxides of sulfur, formed in in this oxidative dehydrogenation process, can be re-oxidized with air and generate useful process heat. Also provided are methods of using the oxide of sulfur oxygen transfer reagent, and an apparatus for effecting the oxidative dehydrogenation of the hydrocarbon feed. Methods of producing the oxide of sulfur oxygen transfer reagent are also provided.

A TRANSPARENT PHOTOCATALYTIC COATING FOR IN-SITU GENERATION OF FREE RADICALS COMBATING MICROBES, ODORS OR ORGANIC COMPOUNDS IN VISIBLE LIGHT
20220152249 · 2022-05-19 ·

A transparent photocatalytic coating for in-situ generation of free radicals combating microbes, odors and organic compounds in visible light is disclosed, featuring a catalytic material comprising a dopant and having particle size distribution suitable for exciton-confinment to accumulatively shift the photocatalytic process into visible light range. Furthermore, the present invention features a method of producing the photocatalytic material described herein. Furthermore, the present invention discloses a method of application of the photocatalytic coating to a surface of a locus. Finally, the present invention features using the photocatalytic coating for removing contaminants and microorganisms at the locus.

Method of preparing supported metallocene catalyst and method of preparing polypropylene using catalyst prepared thereby

Provided are a method of preparing a supported metallocene catalyst, and a method of preparing polypropylene using the catalyst prepared thereby. According to the present invention, provided is a supported metallocene catalyst capable of preparing an isotactic polypropylene polymer having a low xylene soluble content while having excellent catalytic activity.

Processes for producing fluorided solid oxides and uses thereof in metallocene-based catalyst systems

Disclosed herein are methods for preparing fluorided solid oxides by contacting an acidic fluorine-containing compound with an inorganic base to form an aqueous mixture having a pH of at least 4, followed by contacting a solid oxide with the aqueous mixture to produce the fluorided solid oxide. Also disclosed are methods for preparing fluorided solid oxides by contacting an acidic fluorine-containing compound with a solid oxide to produce a mixture, followed by contacting the mixture with a inorganic base to produce the fluorided solid oxide at a pH of at least about 4. The fluorided solid oxide can be used as an activator component in a catalyst system for the polymerization of olefins.