A heterogeneous catalyst suitable for use in alkane dehydrogenation has an active layer that includes alumina and gallia. The active layer is dispersed on a support such as alumina or silica-modified alumina.

The presently disclosed subject matter relates to methods and systems for alkane dehydrogenation. In a particular non-limiting embodiment, the presently disclosed subject matter provides a system for the dehydrogenation of alkanes that includes two or more reactors configured to perform a dehydrogenation reaction of an alkane in the presence of a catalyst to produce an olefin and a catalyst regenerator, coupled to each of the two or more reactors through at least one transfer line to a regenerator, for the regeneration of spent catalyst.

Process for dehydrogenation of alkanesor alkylbenzenes by using metal sulfide catalyst under the presence of small amounts of hydrogen sulfide.

The present invention provides a pyrolysis tube for manufacturing olefin which tube can improve a yield of olefin in a pyrolysis reaction of a hydrocarbon raw material. The pyrolysis tube (1A) for manufacturing olefin includes a tubular base material (2) made of a heat resistant metal material and a dehydrogenating catalyst (4A) which is supported on an inner surface of the tubular base material (2).

The present invention provides a pyrolysis tube for manufacturing olefin which tube can improve a yield of olefin in a pyrolysis reaction of a hydrocarbon raw material. The pyrolysis tube (1A) for manufacturing olefin includes a tubular base material (2) made of a heat resistant metal material and a dehydrogenating catalyst (4A) which is supported on an inner surface of the tubular base material (2).

Fluidizable catalysts for the oxygen-free oxidative dehydrogenation of alkanes to corresponding olefins. The catalysts comprise 10-20% by weight per total catalyst weight of one or more vanadium oxides (VO.sub.x) such as V.sub.2O.sub.5 as well as 1-5% by weight per total catalyst weight of niobium as a promoter. The dehydrogenation catalysts are mounted on an alumina support that is modified with lanthanum to stabilize bulk phase transformation of the alumina. Various methods of preparing and characterizing the catalysts as well as methods for the oxygen-free oxidative dehydrogenation of alkanes to corresponding olefins with improved alkane conversion and olefin selectivity are also disclosed.

Fluidizable catalysts for the oxygen-free oxidative dehydrogenation of alkanes to corresponding olefins. The catalysts comprise 10-20% by weight per total catalyst weight of one or more vanadium oxides (VO.sub.x) such as V.sub.2O.sub.5 as well as 1-5% by weight per total catalyst weight of niobium as a promoter. The dehydrogenation catalysts are mounted on an alumina support that is modified with lanthanum to stabilize bulk phase transformation of the alumina. Various methods of preparing and characterizing the catalysts as well as methods for the oxygen-free oxidative dehydrogenation of alkanes to corresponding olefins with improved alkane conversion and olefin selectivity are also disclosed.

The disclosure provides an improved endothermic hydrocarbon conversion process that comprises reacting a hydrocarbon with a multi-component catalyst bed, and regenerating the catalyst bed with air, where the air used in regeneration step and hydrocarbon are at low air to hydrocarbon ratios and optionally at near-atmospheric pressures.

The disclosure provides an improved endothermic hydrocarbon conversion process that comprises reacting a hydrocarbon with a multi-component catalyst bed, and regenerating the catalyst bed with air, where the air used in regeneration step and hydrocarbon are at low air to hydrocarbon ratios and optionally at near-atmospheric pressures.

A process of catalytically dehydrogenating an alkane to an alkene, using Cr.sub.2O.sub.3 as a catalyst, where the catalyst is reduced concurrently with the dehydrogenation by using CO as a reducing gas. In reducing the catalyst with CO, CO.sub.2 is produced, which may be reacted with H.sub.2 produced by the dehydrogenation, to form CO and H.sub.2O by the reverse water-gas shift reaction. A Cu O heat-releasing material may be included with the catalyst in the reactor. The CO reducing gas reduces CuO to form Cu and CO.sub.2, releasing heat. The CO.sub.2 produced by reducing the Cu O may also be reacted with H.sub.2 produced by the dehydrogenation, to form CO and H.sub.2O by the reverse water-gas shift reaction.