A process for preparing C.sub.2 to C.sub.5 olefins includes introducing a feed stream comprising hydrogen and at least one carbon-containing component selected from the group consisting of CO, CO.sub.2, and mixtures thereof into a reaction zone. The feed stream is contacted with a hybrid catalyst in the reaction zone, and a product stream is formed that exits the reaction zone and includes C.sub.2 to C.sub.5 olefins. The hybrid catalyst includes a methanol synthesis component and a solid microporous acid component that is selected from molecular sieves having 8-MR access and having a framework type selected from the group consisting of CHA, AEI, AFX, ERI, LTA, UFI, RTH, and combinations thereof. The methanol synthesis component comprises a metal oxide support and a metal catalyst. The metal oxide support includes titania, zirconia, hafnia or mixtures thereof, and the metal catalyst includes zinc.

Modified red mud catalyst compositions, methods for production, and methods of use in steam reforming, the composition comprising: red mud material produced from an alumina extraction process from bauxite ore; and nickel oxide, the nickel oxide present at between about 5 wt. % to about 40 wt. % of the modified red mud catalyst composition.

Modified red mud catalyst compositions, methods for production, and methods of use in steam reforming, the composition comprising: red mud material produced from an alumina extraction process from bauxite ore; and nickel oxide, the nickel oxide present at between about 5 wt. % to about 40 wt. % of the modified red mud catalyst composition.

The present invention discloses a series of ammonia decomposition catalysts, the method of making such catalysts and the use of such catalysts. The said catalysts are made of composite metal or metal alloys supported on composite oxides or nitrides as the catalyst supports. The catalysts are useful in ammonia decomposition at various temperatures and pressures, including temperatures below 500° C. and pressures up to 30 atm.

The present invention discloses a series of ammonia decomposition catalysts, the method of making such catalysts and the use of such catalysts. The said catalysts are made of composite metal or metal alloys supported on composite oxides or nitrides as the catalyst supports. The catalysts are useful in ammonia decomposition at various temperatures and pressures, including temperatures below 500° C. and pressures up to 30 atm.

A catalyst comprising Mo, Bi, and Fe, and satisfying, in an X-ray diffraction analysis, 0.10<P/R<0.18 and 0.06<Q/R<0.30 where P represents a peak intensity at 2θ=22.9±0.2°, Q represents a peak intensity at 2θ=28.1±0.1°, and R represents a peak intensity at 2θ=26.6±0.2°.

A catalyst comprising Mo, Bi, and Fe, and satisfying, in an X-ray diffraction analysis, 0.10<P/R<0.18 and 0.06<Q/R<0.30 where P represents a peak intensity at 2θ=22.9±0.2°, Q represents a peak intensity at 2θ=28.1±0.1°, and R represents a peak intensity at 2θ=26.6±0.2°.

This invention relates to a supported catalyst for synthesizing ammonia (NH3) from nitrogen gas (N2) and hydrogen gas (H2), method of making the support, and methods of decorating the support with the catalyst.

This invention relates to a supported catalyst for synthesizing ammonia (NH3) from nitrogen gas (N2) and hydrogen gas (H2), method of making the support, and methods of decorating the support with the catalyst.

A perovskite-type oxide catalyst for water-splitting reactions is provided. The catalyst, Ca.sub.2-ySr.sub.yFe.sub.1-xCo.sub.1-xMn.sub.2xO.sub.6-δ where y=0.10-1.90 and x=0.05-0.95, has catalytic activity for both hydrogen- and oxygen-evolution reactions. An exemplary catalyst is CaSrFe.sub.0.75Co.sub.0.75Mn.sub.0.5O.sub.6-δ.