A process for producing branched alcohols through isomerization, hydroformylation and hydrogenation.

As a hydrocarbon production system that synthesizes hydrocarbons using water and carbon dioxide as raw materials, a hydrocarbon production system capable of producing hydrocarbons by securing hydrogen and carbon monoxide required for hydrocarbon synthesis is provided. In a hydrocarbon production system that produces hydrocarbons from at least water and carbon dioxide, the hydrocarbon production system includes at least an electrolytic reaction unit, a reverse water-gas shift reaction unit, and a hydrocarbon synthesis reaction unit.

A process for producing branched alcohols through isomerization, hydroformylation and hydrogenation.

A hydrocarbon production system capable of efficiently producing hydrocarbon containing a high-calorie gas by securing hydrogen and carbon monoxide required for hydrocarbon synthesis using water and carbon dioxide as raw materials is obtained. The hydrocarbon production system includes an electrolytic reaction unit that converts water and carbon dioxide into hydrogen and carbon monoxide through an electrolytic reaction, a catalytic reaction unit that converts a product generated by the electrolytic reaction unit into hydrocarbon through a catalytic reaction, and branch paths and that branch a portion of an outlet component of the catalytic reaction unit.

Methods of converting ethane to ethylene at relatively low temperatures are described. IrO.sub.2-based catalysts are used in the conversion. Methods of converting a base gas to a first gas by exposing the base gas to an IrO.sub.2-based catalyst and forming the first gas are described. The base gas can be an alkane. The first gas can include an alkene, an alkyne, an alcohol, an aldehyde, or combinations thereof.

The present disclosure relates to a multi-sandwich composite catalyst and a preparation method and application thereof. The present disclosure provides a preparation method of a multi-sandwich composite catalyst, comprises the following steps: sequentially depositing a first layer oxide, a first active metal, an oxide interlayer, a second active metal and a surface oxide on a template, and sequentially performing calcination and reduction, thereby obtaining a multi-sandwich composite catalyst; wherein the first active metal and the second active metal are different kinds of active metals. In the present disclosure, a multi-sandwich structure is formed by depositing the oxides and active metals alternately, so that the position and spacing distance of the active centers can be precisely controlled. The multi-sandwich composite catalyst prepared by the method provided described herein has a higher conversion than that of a catalyst without an interlayer when used for the catalytic reaction.

A methane (CH.sub.4) gas is synthesized from carbon dioxide (CO.sub.2) and hydrogen (H.sub.2) using catalyst-dielectric barrier discharge (DBD) plasma at room temperature and atmospheric pressure. In the method and apparatus for synthesizing methane gas of the invention, methane (CH.sub.4) gas, which is synthetic natural gas, can be effectively synthesized only from carbon dioxide (CO.sub.2) and hydrogen (H.sub.2) using DBD plasma at room temperature and atmospheric pressure, and also, additional heating and pressurization devices are not used during the methane gas synthesis process, thus reducing production costs and realizing high-value-added processing due to the absence of risks during the processing.

A three step method for the conversion of ethanol into fuels that can be utilized as full-performance military jet or diesel fuels. Embodiments of the invention further describe methods for the selective conversion of ethanol to full performance saturated hydrocarbon fuels that are suitable for both jet and diesel propulsion.

A process for producing branched alcohols through isomerization, hydroformylation and hydrogenation.

Increase propane dehydrogenation activity of a partially deactivated dehydrogenation catalyst by heating the partially deactivated catalyst to a temperature of at least 660° C., conditioning the heated catalyst in an oxygen-containing atmosphere and, optionally, stripping molecular oxygen from the conditioned catalyst.