A catalyst for the dehydrogenation of alkanes to alkenes comprises a catalytically active material supported on a carrier, wherein the catalytically active material is a metallic sulfide (MeS) comprising Fe, Co, Ni, Cu, Mo or W or any combination of two or more metals selected from Pb, Sn, Zn, Fe, Co, Ni, Cu, Mo and W. The catalyst is regenerated in several steps. The dehydrogenation is carried out at a temperature between 450 and 650 C. and a pressure from 0.9 bar below ambient pressure to 5 bar above ambient pressure.

Methods, catalysts, and systems for the production of 1,3-butadiene from a reaction mixture including ethylene and gaseous sulfur are described.

Disclosed is a catalyst and methods for the oxidative coupling of methane (OCM) reaction using elemental sulfur as a soft oxidant. The process can provide ethylene from methane with high conversion and selectivity.

Methods for oxidative coupling of methane using metal oxide catalysts and a sulfur oxidant.

A catalyst for the dehydrogenation of alkanes to alkenes comprises a catalytically active material supported on a carrier, wherein the catalytically active material is a metallic sulfide (MeS) comprising Fe, Co, Ni, Cu, Mo or W or any combination of two or more metals selected from Pb, Sn, Zn, Fe, Co, Ni, Cu, Mo and W. The catalyst is regenerated in several steps. The dehydrogenation is carried out at a temperature between 450 and 650 C. and a pressure from 0.9 bar below ambient pressure to 5 bar above ambient pressure.

The present invention relates to a stabilized rhenium-based heterogeneous catalyst, obtainable by a process comprising contacting a rhenium-based heterogeneous catalyst with a stabilizing agent at a temperature in a range from 0-100 C., the stabilizing agent comprising an aliphatic hydrocarbon compound and use thereof.

Disclosed herein are carbon doped tin disulphide (CSnS.sub.2) and other SnS.sub.2 composites as visible light photocatalyst for CO.sub.2 reduction to solar fuels. The in situ carbon doped SnS.sub.2 photocatalyst provide higher efficiency than the undoped pure SnS.sub.2. Also disclosed herein are methods for preparing the catalysts.

Methods for selectively hydrogenating substituted arenes with a supported organometallic hydrogenating catalyst are provided. An exemplary method includes contacting a substituted arene-containing reaction stream with hydrogen in the presence of a supported organometallic hydrogenating catalyst under reaction conditions effective to selectively hydrogenate the substituted arenes to the cis isomer with high selectivity. In this method, the supported organometallic hydrogenating catalyst includes a catalytically active organometallic species and a Brnsted acidic sulfated metal oxide support.