Disclosed are a catalyst used for converting carbon dioxide to methanol by hydrogenation and a method preparing the sane. The caratlys may include: a mesoporous indium oxide; and a catalyst supported on the mesoporous indium oxide. Preferably, a porous structure of the mesoporous indium oxide may have Ia3d symmetry and may include mesopores and micropores interconnecting the mesopores.

The present disclosure relates to a dehydrogenation catalyst for use in dehydrogenation of a branched light hydrocarbon gas, the catalyst including platinum, tin, and an alkali metal which are carried in a phase-changed carrier, in which platinum and tin form a single complex and are present in an alloy form within a predetermined thickness from the outer surface of the catalyst.

An activated carbon/palladium-gallium (Pd—Ga) liquid alloy composite catalyst, including a support and an active component supported on the support. The support is acid washed activated carbon. The active component is Pd—Ga liquid alloy. In the present invention, the active component Pd—Ga, present in the form of liquid alloy, forms a self-protective oxide layer. This protects acetylene from secondary reactions on the surface of the catalyst, inhibits or reduces acetylene to deeply hydrogenate to form ethane, thereby increasing ethylene selectivity. The present invention further provides a preparation method of the catalyst, where the catalyst of the present invention is prepared by immersion. The preparation method is simple and easy to operate. When the activated carbon/Pd—Ga liquid alloy composite catalyst provided by the present invention is used for acetylene hydrogenation to prepare ethylene, conversion rate of acetylene is as high as 99.8%, while the ethylene selectivity is as high as 98.9%.

An activated carbon/palladium-gallium (Pd—Ga) liquid alloy composite catalyst, including a support and an active component supported on the support. The support is acid washed activated carbon. The active component is Pd—Ga liquid alloy. In the present invention, the active component Pd—Ga, present in the form of liquid alloy, forms a self-protective oxide layer. This protects acetylene from secondary reactions on the surface of the catalyst, inhibits or reduces acetylene to deeply hydrogenate to form ethane, thereby increasing ethylene selectivity. The present invention further provides a preparation method of the catalyst, where the catalyst of the present invention is prepared by immersion. The preparation method is simple and easy to operate. When the activated carbon/Pd—Ga liquid alloy composite catalyst provided by the present invention is used for acetylene hydrogenation to prepare ethylene, conversion rate of acetylene is as high as 99.8%, while the ethylene selectivity is as high as 98.9%.

Systems and methods for producing butadiene are disclosed. In a reaction unit, n-butane is dehydrogenated in the presence of a double-dehydrogenation catalyst to produce a mixture that includes butadiene and unreacted n-butane. An extractive distillation unit that uses soybean oil as the solvent is utilized to extract at least some of the unreacted n-butane from the mixture.

Systems and methods for producing butadiene are disclosed. In a reaction unit, n-butane is dehydrogenated in the presence of a double-dehydrogenation catalyst to produce a mixture that includes butadiene and unreacted n-butane. An extractive distillation unit that uses soybean oil as the solvent is utilized to extract at least some of the unreacted n-butane from the mixture.

A process is provided for dehydrogenating a paraffinic hydrocarbon comprising sending the paraffinic hydrocarbon to a fluidized bed reactor to be contacted at dehydrogenation reaction conditions with a catalyst composition comprising less than about 0.0999 wt % platinum and about 0.05-2.5 wt % Group I or Group II elements or a mixture thereof. The catalytic composition is prepared without addition of tin, gallium, indium, germanium or lead.

Systems and methods of dehydrogenating a hydrocarbon in a fixed bed dehydrogenation unit. A method for dehydrogenating a hydrocarbon is applied to a fixed bed reactor. The hydrocarbon flows to a fixed bed reactor to be dehydrogenated in presence of a catalyst in the fixed bed reactor. The catalyst in the fixed bed reactor is then regenerated. The period for dehydrogenation, the period for catalyst regeneration and the period for total slack time are controlled such that total slack time is less than both half of the period for dehydrogenation and half of the period for regeneration. One of the advantages of the process comes from optimization of the slack time, thereby increasing the catalyst utilization rate and number of reactors concurrently online.

A process for dehydrogenating alkane or alkylaromatic compounds comprising contacting the given compound and a dehydrogenation catalyst in a fluidized bed. The dehydrogenation catalyst is prepared from an at least partially deactivated platinum/gallium catalyst on an alumina-based support that is reconstituted by impregnating it with a platinum salt solution, then calcining it at a temperature from 400° C. to 1000° C., under conditions such that it has a platinum content ranging from 1 to 500 ppm, based on weight of catalyst; a gallium content ranging from 0.2 to 2.0 wt %; and a platinum to gallium ratio ranging from 1:20,000 to 1:4. It also has a Pt retention that is equal to or greater than that of a fresh catalyst being used in a same or similar catalytic process.

A process for dehydrogenating alkane or alkylaromatic compounds comprising contacting the given compound and a dehydrogenation catalyst in a fluidized bed. The dehydrogenation catalyst is prepared from an at least partially deactivated platinum/gallium catalyst on an alumina-based support that is reconstituted by impregnating it with a platinum salt solution, then calcining it at a temperature from 400° C. to 1000° C., under conditions such that it has a platinum content ranging from 1 to 500 ppm, based on weight of catalyst; a gallium content ranging from 0.2 to 2.0 wt %; and a platinum to gallium ratio ranging from 1:20,000 to 1:4. It also has a Pt retention that is equal to or greater than that of a fresh catalyst being used in a same or similar catalytic process.