B01J23/18

Multi-zoned catalyst system for oxidation of o-xylene and/or naphthalene to phthalic anhydride

The present invention relates to a catalyst system for oxidation of o-xylene and/or naphthalene to phthalic anhydride (PA) comprising at least four catalyst zones arranged in succession in the reaction tube and filled with catalysts of different chemical composition wherein the active material of the catalysts comprise vanadium and titanium dioxide and the active material of the catalyst in the last catalyst zone towards the reactor outlet has an antimony content (calculated as antimony trioxide) between 0.7 to 3.0 wt. %. The present invention further relates to a process for gas phase oxidation in which a gas stream comprising at least one hydrocarbon and molecular oxygen is passed through a catalyst system which comprises at least four catalyst zones arranged in succession in the reaction tube and filled with catalysts of different chemical composition wherein the active materials of the catalysts comprise vanadium and titanium dioxide and the active material of the catalyst in the last catalyst zone towards the reactor outlet has an antimony content (calculated as antimony trioxide) between 0.7 to 3.0 wt. %.

Oxygen-free direct conversion of methane and catalysts therefor

A process of methane catalytic conversion produces olefins, aromatics, and hydrogen under oxygen-free, continuous flowing conditions. Such a process has little coke deposition and realizes atom-economic conversion. Under the conditions encountered in a fixed bed reactor (i.e. reaction temperature: 750-1200 C.; reaction pressure: atmospheric pressure; the weight hourly space velocity of feed gas: 1000-30000 ml/g/h; and fixed bed), conversion of methane is 8-50%. The selectivity of olefins is 30-90%. And selectivity of aromatics is 10-70%. The catalyst for this methane conversion has a SiO.sub.2-based matrix having active species that are formed by confining dopant metal atoms in the lattice of the matrix.

Oxygen-free direct conversion of methane and catalysts therefor

A process of methane catalytic conversion produces olefins, aromatics, and hydrogen under oxygen-free, continuous flowing conditions. Such a process has little coke deposition and realizes atom-economic conversion. Under the conditions encountered in a fixed bed reactor (i.e. reaction temperature: 750-1200 C.; reaction pressure: atmospheric pressure; the weight hourly space velocity of feed gas: 1000-30000 ml/g/h; and fixed bed), conversion of methane is 8-50%. The selectivity of olefins is 30-90%. And selectivity of aromatics is 10-70%. The catalyst for this methane conversion has a SiO.sub.2-based matrix having active species that are formed by confining dopant metal atoms in the lattice of the matrix.

SEMICONDUCTOR NANOCRYSTALS

Present subject matter provides a semiconductor nanocrystal comprises a core and a shell. The core is fabricated from a first semiconductor. The shell is fabricated from a second semiconductor. The optical cross section of the semiconductor nanocrystal is in a range of 10.sup.17 cm.sup.2-10.sup.12 cm.sup.2 in a 2-3 eV region. The core is less than 2 nanometers from an outer surface of the shell in at least one region of the semiconductor nanocrystal. Present subject matter also provides method for preparation of the semiconductor nanocrystals and method for photosynthesis of organic compounds.

Process for catalytic oxidative dehydrogenation of ethane to ethylene in the presence of chlorine intermediates
10669218 · 2020-06-02 · ·

A process for producing ethylene comprising: (a) reacting a reactant mixture in a reactor to yield a product mixture, wherein the reactor comprises a catalyst, wherein the reactant mixture comprises ethane, oxygen, and a chlorine intermediate precursor, wherein the product mixture comprises ethylene, unreacted ethane, carbon monoxide, and carbon dioxide, wherein the catalyst comprises a redox agent, an alkali metal, and a rare earth element; and (b) recovering at least a portion of the ethylene from the product mixture. The reacting in step (a) further comprises (i) contacting at least a portion of the chlorine intermediate precursor with the catalyst to form a chlorinated catalyst; (ii) allowing at least a portion of the chlorinated catalyst to generate a chlorine intermediate; and (iii) allowing at least a portion of the reactant mixture to react via the chlorine intermediate.

HIGH ACTIVITY, HIGH GASOLINE YIELD AND LOW COKE FLUID CATALYTIC CRACKING CATALYST
20200157434 · 2020-05-21 ·

A microspherical fluid catalytic cracking (FCC) catalyst includes a zeolite and alumina comprising a strong Lewis site density of less than 70 .Math.ol/g.

Electrodeposition system

An electrocoat system for electrodeposition is described. The system includes an inorganic bismuth-containing compound or a mixture of inorganic and organic bismuth-containing compounds. The system demonstrates a high degree of crosslinking and produces a cured coating with optimal crosslinking and corrosion resistance.

Electrodeposition system

An electrocoat system for electrodeposition is described. The system includes an inorganic bismuth-containing compound or a mixture of inorganic and organic bismuth-containing compounds. The system demonstrates a high degree of crosslinking and produces a cured coating with optimal crosslinking and corrosion resistance.

Shaped porous carbon products

Shaped porous carbon products and processes for preparing these products are provided. The shaped porous carbon products can be used, for example, as catalyst supports and adsorbents. Catalyst compositions including these shaped porous carbon products, processes of preparing the catalyst compositions, and various processes of using the shaped porous carbon products and catalyst compositions are also provided.

Method for preparing carboxylic esters from aldehydes

A method can prepare a carboxylic ester. The method includes reacting an aldehyde in the presence of an aluminium alkoxide applied to a support material.