The present invention provides a catalyst for aromatization of a long-carbon chain alkane and a preparation method thereof. In the present invention, a molecular sieve containing a BEA structure is taken as an active component and mixed with a carrier, and then the mixture is formed, dried and calcined to obtain the catalyst for aromatization of a long-carbon chain alkane. The active component is prepared by taking a Naβ molecular sieve as a raw material and modifying through the following steps of: first obtaining an Hβ molecular sieve through ammonium ion-exchange, and then conducting dealumination and silicon insertion treatment of the Hβ molecular sieve through first hydrothermal treatment; forming a mesoporous structure in a molecular sieve framework through second hydrothermal treatment; reducing the acidity of the catalyst by potassium ion exchange, and finally using metal modification to improve the capability of the catalyst for catalyzing the aromatization of the long-carbon chain alkane and enhancing the toluene selectivity. The catalyst provided by the present invention shows high stability in the aromatization of the long-chain alkane and has a service life up to 170 h or above and aromatic hydrocarbon selectivity up to 80%, and the selectivity to toluene in aromatic hydrocarbon products can reach 85.5%.

The present disclosure relates to the catalytic field, and discloses a catalyst system and a light hydrocarbon aromatization method, a carbon dioxide hydrogenation process and a method for enhancing the catalytic activity and/or lifetime of the catalyst during a heterogeneous catalysis process, the catalyst system comprising a porous material layer containing an active metal component and a molecular sieve layer. The catalyst system provided by the present disclosure exhibits desirable catalytic activity, stability, renewability and selectivity, thus has significant benefits.

The present invention provides a catalyst for aromatization of a long-carbon chain alkane and a preparation method thereof. In the present invention, a molecular sieve containing a BEA structure is taken as an active component and mixed with a carrier, and then the mixture is formed, dried and calcined to obtain the catalyst for aromatization of a long-carbon chain alkane. The active component is prepared by taking a Naβ molecular sieve as a raw material and modifying through the following steps of: first obtaining an Hβ molecular sieve through ammonium ion-exchange, and then conducting dealumination and silicon insertion treatment of the Hβ molecular sieve through first hydrothermal treatment; forming a mesoporous structure in a molecular sieve framework through second hydrothermal treatment; reducing the acidity of the catalyst by potassium ion exchange, and finally using metal modification to improve the capability of the catalyst for catalyzing the aromatization of the long-carbon chain alkane and enhancing the toluene selectivity. The catalyst provided by the present invention shows high stability in the aromatization of the long-chain alkane and has a service life up to 170 h or above and aromatic hydrocarbon selectivity up to 80%, and the selectivity to toluene in aromatic hydrocarbon products can reach 85.5%.

The present disclosure relates to the catalytic field, and discloses a catalyst system and a light hydrocarbon aromatization method, a carbon dioxide hydrogenation process and a method for enhancing the catalytic activity and/or lifetime of the catalyst during a heterogeneous catalysis process, the catalyst system comprising a porous material layer containing an active metal component and a molecular sieve layer. The catalyst system provided by the present disclosure exhibits desirable catalytic activity, stability, renewability and selectivity, thus has significant benefits.

An oxidative dehydrogenation catalyst having: a structure having a formula Mo.sub.vV.sub.wNb.sub.yBi.sub.zO.sub.x, where v is 1, w is from 0.1 to 0.5, y is from 0.001 to 0.3, z is from 0.01 to 0.3, and x is the oxygen content required to charge-balance the structure. The oxidative dehydrogenation catalyst has a Pba2-32 space group, characterized by reflections determined with CuK.sub. X-ray diffraction (XRD) as follows.

Process for catalytic oxidative esterification of methacrolein with methanol and oxygen to methyl methacrylate in the presence of a heterogeneous egg-shell catalyst comprising gold metal and an oxide of at least one second element selected from Ni, Co, Fe, Zn and/or Ti supported on a support material comprising SiO.sub.2, Al.sub.2O.sub.3 and at least one basic element oxide, characterized in that the process is carried out in the presence of at least one compound, comprising Ni, Co, Fe, Zn and/or Ti, which is soluble in the reaction mixture under process conditions.

A method for producing trifluoroethylene in a reactor with a fixed catalytic bed comprising a catalyst, comprises the steps of: a) reacting chlorotrifluoroethylene with hydrogen in the presence of the catalyst and in the gas phase, to produce a flow of product comprising trifluoroethylene; b) treating the flow of product obtained in step a) in order to recover a stream A comprising trifluoroethylene, chlorotrifluoroethylene and an additional compound selected from the group consisting of 1,1-difluoroethylene, 1,1,1,2-tetrafluoroethane, 1,1,1-trifluoroethane and ethane; wherein the total content by weight of the additional compound is less than 0.5%; c) distilling stream A to recover a stream B comprising at least 99% by weight of trifluoroethylene and less than 0.2% by weight of one or more additional compounds. A composition comprising at least 99% by weight of trifluoroethylene and from 0.1 to 1000 ppm of ethane, and/or from 0.1 to 1000 ppm of 1,1,1,2-tetrafluoroethane, based on the total weight of the composition is disclosed.

HFO-1132 and, in particular, HFO-1132E, may be produced from 1,1,2-trichloro-1,2,2-trifluoroethane (CFC-113). In a first step, 1,1,2-trifluoroethane (HFC-143) is produced by hydrogenating 1,1,2-trichloro-1,2,2-trifluoroethane (CFC-113) by reaction with hydrogen in the presence of a catalyst to produce 1, 1,2-trifluoroethane (HFC-143). The highly exothermic hydrogenation step may be moderated by diluting the catalyst and/or by diluting the 1, 1,2-trichloro-1,2,2-trifluoroethane (CFC-113) feedstock. The 1, 1,2-trifluoroethane (HFC-143) may then be dehydrofluorinated in the presence of a catalyst to produce trans-1,2-difluoroethylene (HFO-1132E) and/or cis-1,2-difluoroethylene (HFO-1132Z). The cis-1,2-difluoroethylene (HFO-1132Z) may then be isomerized to produce trans-1,2-difluoroethylene (HFO-1132E).

Shaped catalyst compositions and methods for making and using the shaped catalyst compositions are provided. In an exemplary a catalyst active phase includes a MoVTeNbOx catalyst. The composition also includes a support phase, wherein the support phase includes fumed silica, and wherein the catalyst active phase and support phase form a heterogeneous mixture.