The present technology is directed to processes for conversion of synthesis gas in a tubular reactor to produce a synthetic product that utilizes high activity carbon monoxide hydrogenation catalysts and a heat transfer structure that surprisingly provides for higher per pass conversion with high selectivity for the desired synthetic product without thermal runaway.

A reactor includes: a main reactor core including main reaction flow channels through which the raw material fluid flows, and main temperature control flow channels through which the heat medium flows along a flow direction of the raw material fluid flowing in the main reaction flow channel; and a pre-reactor core including pre-reaction flow channels of which an outlet side connects with an inlet side of the main reaction flow channels and through which the raw material fluid flows, and pre-temperature control flow channels of which an inlet side connects with an outlet side of the main reaction flow channels and through which the product serving as the heat medium flows along a flow direction of the raw material fluid flowing in the pre-reaction flow channel.

The present technology is directed to processes for conversion of synthesis gas in a tubular reactor to produce a synthetic product that utilizes high activity carbon monoxide hydrogenation catalysts and a heat transfer structure that surprisingly provides for higher per pass conversion with high selectivity for the desired synthetic product without thermal runaway.

The present disclosure provides oxidative coupling of methane (OCM) systems for small scale and world scale production of olefins. An OCM system may comprise an OCM subsystem that generates a product stream comprising C.sub.2+ compounds and non-C.sub.2+ impurities from methane and an oxidizing agent. At least one separations subsystem downstream of, and fluidically coupled to, the OCM subsystem can be used to separate the non-C.sub.2+ impurities from the C.sub.2+ compounds. A methanation subsystem downstream and fluidically coupled to the OCM subsystem can be used to react H.sub.2 with CO and/or CO.sub.2 in the non-C.sub.2+ impurities to generate methane, which can be recycled to the OCM subsystem. The OCM system can be integrated in a non-OCM system, such as a natural gas liquids system or an existing ethylene cracker.

An apparatus for producing a natural gas using carbon dioxide and water in air that includes an air-compressing member, a water collecting member, a water storing member, a carbon dioxide collecting member, a water electrolysis member, and a methanation reaction member. The water electrolysis member electrolyzes water separated from compressed air. The methanation reaction member generates a natural gas by reacting hydrogen from the electrolysis and carbon dioxide from the carbon dioxide collecting member. A method of producing a natural gas using carbon dioxide and water in air includes supplying hydrogen electrolyzed from water separated from air and carbon dioxide collected from the dry air to a methanation reaction member to generate a natural gas. A natural gas-synthesizing equipment system includes an apparatus for producing a natural gas using carbon dioxide and water in air.

The method for recycling carbon dioxide according to the present invention includes: injecting a reaction gas containing carbon dioxide and a carbon raw material into a rotary heating furnace; reacting the reaction gas and the carbon raw material with each other in the rotary heating furnace to generate a hydrocarbon precursor containing carbon monoxide; and converting the hydrocarbon precursor into a hydrocarbon compound, thereby exhibiting excellent conversion rate of carbon dioxide.

The invention relates to an arrangement for preparing a gas in a closable reactor by supplying the reactor with carbon-based biomass or chopped wood material, such as chips, in substantially oxygen-free conditions, by allowing the biomass or wood material to gasify at a high temperature, and by recovering the gas generated in a gasification reaction. In that the arrangement the reactor has its interior defined by a feed pipe whose inlet end is closable with a shut-off valve, especially with a ball valve, and whose outlet end adjoins a heatable gasification dome, biomass or chopped wood material is delivered from the feed pipe's inlet end into the reactor's interior, the reactor's interior is supplied with free water/water vapor in its supercritical state, which is optionally prepared catalytically by splitting water/water vapor, the biomass or wood material is conveyed into a gasification space of the reactor's interior, which is in connection with the heated gasification dome and which is adapted to have existing conditions selected in a manner such that the water present in said gasification space is present in its supercritical state, and the gas generated in the gasification reaction is recovered.

The invention relates to a method for converting a gas into methane (CH4) which includes: a step of activating a catalytic material including praseodymium oxide (Pr6O11) associated with nickel oxide (NiO) and alumina (Al2O3), the respective proportions of which are, relative to the total mass of these three compounds:

Pr6O11: 1 wt % to 20 wt %,

NiO: 1 wt % to 20 wt %, and

A12O3: 60 to 98 wt %; and a step of passing a gas including at least one carbon monoxide (CO) over the activated catalytic material.

The invention relates to Fischer-Tropsch synthesis in a compact version. A compact reactor comprises a housing, rectangular reaction channels inside the housing, which are filled with a cobalt catalyst, synthesis gas injection nozzles in the number determined by the ratio of the number of channels to the number of synthesis gas injection nozzles, an input and output nozzle for heat transfer medium on which a pressure controller installed, and an assembly for withdrawing synthetic hydrocarbons. The cobalt catalyst is activated by passing hydrogen through it. Synthetic hydrocarbons are produced by passing synthesis gas through the reaction channels filled with the activated cobalt catalyst. The space velocity of synthesis gas is increased every 300-500 h, followed by returning to the initial process conditions. This provides a high-molecular-weight hydrocarbon output per unit mass of the reactor.

The present disclosure provides oxidative coupling of methane (OCM) systems for small scale and world scale production of olefins. An OCM system may comprise an OCM subsystem that generates a product stream comprising C.sub.2+ compounds and non-C.sub.2+ impurities from methane and an oxidizing agent. At least one separations subsystem downstream of, and fluidically coupled to, the OCM subsystem can be used to separate the non-C.sub.2+ impurities from the C.sub.2+ compounds. A methanation subsystem downstream and fluidically coupled to the OCM subsystem can be used to react H.sub.2 with CO and/or CO.sub.2 in the non-C.sub.2+ impurities to generate methane, which can be recycled to the OCM subsystem. The OCM system can be integrated in a non-OCM system, such as a natural gas liquids system or an existing ethylene cracker.