The method of the present invention for producing 1,3-butadiene includes: vaporizing an ethanol feedstock in a vaporizer (104), supplying the feedstock to two or more parallel first reactors (108) to convert ethanol into acetaldehyde in the presence of a first catalyst; supplying a resulting intermediate gas to a second reactor (110) to convert ethanol and acetaldehyde into 1,3-butadiene in the presence of a second catalyst; purifying a resulting crude gas containing 1,3-butadiene by a gas-liquid separator (112), a first distillation column (114), a fourth reactor (116), and a second distillation column (118); and supplying an oxygen-containing gas to at least one of the two or more parallel first reactors (108) under specific conditions, while discharging a carbon dioxide-containing gas from the first reactor (108), to thereby regenerate the first catalyst, while continuing the conversion reaction.

In the method of the present invention, 1,3-butadiene is produced by vaporizing an ethanol feedstock in a vaporizer (104), feeding the resulting into two or more parallel first reactors (108) to convert the ethanol to acetaldehyde in the presence of a first catalyst, supplying the resulting intermediate gas to a second reactor (110) to convert the ethanol and acetaldehyde to 1,3-butadiene in the presence of a second catalyst, purifying the resulting crude gas containing 1,3-butadiene by a gas-liquid separator (112), a first distillation column (114), a fourth reactor (116), a second distillation column (118), and mixing one of both of a part of the ethanol-containing gas and an acetaldehyde-containing gas obtained in the second distillation column (118) are mixed with the intermediate gas, thereby adjusting an ethanol/acetaldehyde molar ratio in the intermediate gas to 1 to 100.

A supported catalyst for preparing light olefin using direct conversion of syngas is a composite catalyst and formed by compounding component I and component II in a mechanical mixing mode. The active ingredient of component I is a metal oxide; and the component II is a supported zeolite. A carrier is one or more than one of hierarchical pores Al.sub.2O.sub.3, SiO.sub.2, TiO.sub.2, ZrO.sub.2, CeO.sub.2, MgO and Ga.sub.2O.sub.3; the zeolite is one or more than one of CHA and AEI structures; and the load of the zeolite is 4%-45% wt. A weight ratio of the active ingredients in the component I to the component II is 0.1-20. The reaction process has an extremely high light olefin selectivity; the sum of the selectivity of the light olefin comprising ethylene, propylene and butylene can reach 50-90%, while the selectivity of a methane side product is less than 7%.

The present invention relates to a catalyst which is a composite oxide including at least one element X selected from the group consisting of elements belonging to Groups 3 to 6 of the periodic table, and at least one element Z selected from the group consisting of elements belonging to Group 14 of the periodic table, wherein the catalyst has mesopores.

A catalyst includes at least one element X selected from the group consisting of Groups 3 to 6 of the Periodic Table, and at least one element Z selected from the group consisting of Group 14 elements. At least one diffraction peak is observed in a low angle range of θ=6° or less in an X-ray diffraction profile observed using X-ray diffraction. The at least one diffraction peak has a ratio (I/H) of a peak intensity I to a half width at half maximum H of the diffraction peak of 5000 or more.

The method of the present invention for producing 1,3-butadiene includes: vaporizing an ethanol feedstock in a vaporizer (104), supplying the feedstock to two or more parallel first reactors (108) to convert ethanol into acetaldehyde in the presence of a first catalyst; supplying a resulting intermediate gas to a second reactor (110) to convert ethanol and acetaldehyde into 1,3-butadiene in the presence of a second catalyst; purifying a resulting crude gas containing 1,3-butadiene by a gas-liquid separator (112), a first distillation column (114), a fourth reactor (116), and a second distillation column (118); and supplying an oxygen-containing gas to at least one of the two or more parallel first reactors (108) under specific conditions, while discharging a carbon dioxide-containing gas from the first reactor (108), to thereby regenerate the first catalyst, while continuing the conversion reaction.

Disclosed is a method of producing an olefin using a circulating fluidized bed process, including: (a) supplying a hydrocarbon mixture including propane and a dehydrogenation catalyst to a riser which is in a state of a fast fluidization regime, and thus inducing a dehydrogenation reaction; (b) separating an effluent from the dehydrogenation reaction into the catalyst and a propylene mixture; (c) stripping, in which a residual hydrocarbon compound is removed from the catalyst separated in step (b); (d) mixing the catalyst stripped in step (c) with a gas containing oxygen and thus continuously regenerating the catalyst; (e) circulating the catalyst regenerated in step (d) to step (a) and thus resupplying the catalyst to the riser; and (f) cooling, compressing, and separating the propylene mixture, which is a reaction product separated in step (b), and thus producing a propylene product.

The present invention relates to a catalyst for isomerization of alkylated aromatics such as mixed xylenes, using xylene isomerization catalyst particles including post-framework modified USY zeolite in which zirconium atoms and/or titanium atoms and/or hafnium atoms form a part of a framework of an ultra-stable Y-type zeolite.

A process for the preparation of a composition comprising oxygenates and hydrocarbons by means of a Fischer-Tropsch synthesis reaction, said process comprising contacting a mixture of hydrogen, carbon monoxide, and carbon dioxide gases with a supported Co—Mn Fischer-Tropsch synthesis catalyst, wherein the supported synthesis catalyst comprises at least 2.5 wt % of manganese, on an elemental basis, based on the total weight of the supported synthesis catalyst; the weight ratio of manganese to cobalt, on an elemental basis, is 0.2 or greater; and, wherein carbon dioxide is present in the Fischer-Tropsch synthesis reaction is at least 5% v/v.

A method for preparing C.sub.2 to C.sub.5 paraffins including introducing a feed stream of hydrogen gas and a carbon-containing gas selected from carbon monoxide, carbon dioxide, and mixtures thereof into a reaction zone of a reactor. Converting the feed stream into a product stream that includes C.sub.2 to C.sub.5 paraffins in the reaction zone in the presence of a hybrid catalyst. The hybrid catalyst including a microporous catalyst component; and a metal oxide catalyst component. The metal oxide catalyst component including a metal component present on a metal oxide support material. The metal oxide support material includes at least one oxide of a metal selected from Group 4 of the IUPAC periodic table of elements. The product stream has a C.sub.3/C.sub.2 carbon molar ratio greater than or equal to 4.0.