The present disclosure relates generally to processes for the Fischer-Tropsch production of hydrocarbons from methane. In particular, the disclosure provides for a process for the production of hydrocarbons and/or oxygenates, the process comprising: reforming a reforming feed comprising methane with water and/or oxygen to produce a reforming product stream comprising carbon monoxide and hydrogen; and contacting a hydrocarbon synthesis mixture comprising hydrogen and carbon monoxide with a Fischer-Tropsch hydrocarbon synthesis catalyst, wherein the hydrocarbon synthesis mixture comprises at least a portion of the reforming product stream to produce a hydrocarbon product stream with a selectivity for C.sub.5+ hydrocarbons of at least 50%, and/or a selectivity for oxygenates of at least 20%.

The present disclosure relates to the technical field of Fischer-Tropsch synthesis reaction catalysts, and discloses a supported / iron carbide catalyst for Fischer-Tropsch synthesis reaction, preparation method thereof and Fischer-Tropsch synthesis process, wherein the method comprises the following steps: (1) dipping a catalyst carrier in a ferric salt aqueous solution, drying and roasting the dipped carrier to obtain a catalyst precursor; (2) subjecting the catalyst precursor and H.sub.2 to a precursor reduction at the temperature of 300-550 C.; (3) pretreating the material obtained in the step (2) with H.sub.2 and CO at the temperature of 90-185 C., wherein the molar ratio of H.sub.2/CO is 1.2-2.8:1; (4) preparing carbide with the material obtained in the step (3), H.sub.2 and CO at the temperature of 200-300 C., wherein the molar ratio of H.sub.2/CO is 1.0-3.2:1. The preparation method has the advantages of simple and easily obtained raw materials, simple and convenient operation steps, being capable of preparing the catalyst with 100% pure phase / iron carbide as the active phase, the catalyst has lower selectivity of CO.sub.2 and CH.sub.4 and higher selectivity of effective products.

Production of fuels from low carbon electricity and from carbon dioxide by the use of a solid oxide electrolysis cell (SOEC) and Fischer-Tropsch is shown. Fischer-Tropsch is an exothermic reaction that can be used to produce steam. Steam produced from the Liquid Fuel Production (LFP) reactor system, where the Fischer-Tropsch reaction occurs, is used as feed to the SOEC. The higher temperature steam improves the efficiency of the overall electrolysis system. The integration of the LFP steam improves the efficiency of the electrolysis because the heat of vaporization for the liquid water does not have to be supplied by the electrolyzer.

The present invention relates to the conversion of flue gas to valuable products, in particular to the conversion of carbon dioxide in flue gas to liquid fuels and valuable carbons in a carbon negative manner.

Method and apparatus for compact and easily maintainable waste reformation. Some embodiments include a rotary oven reformer adapted and configured to provide synthesis gas from organic waste. Some embodiments include a rotary oven with simplified operation both as to reformation of the waste, usage of the synthesized gas and other products, and easy removal of the finished waste products, preferably in a unit of compact size for use in austere settings. Yet other embodiments include Fischer-Tropsch reactors of synthesized gas. Some of these reactors include heat exchanging assemblies that provide self-cleaning effects, efficient utilization of waste heat, and ease of cleaning.

Processes for producing high biogenic concentration Fischer-Tropsch liquids derived from the organic fraction of municipal solid wastes (MSW) feedstock that contains a relatively high concentration of biogenic carbon (derived from plants) and a relatively low concentration of non-biogenic carbon (derived from fossil sources) wherein the biogenic content of the Fischer-Tropsch liquids is the same as the biogenic content of the feedstock.

The invention provides a process for preparing liquid fuels and chemicals, which process comprises feeding carbon monoxide and hydrogen to a hydrogenation reactor, wherein the molar ratio CO:H.sub.2 is in the range of 1:0.5 to 1:0.9, catalytically hydrogenating said carbon monoxide in said hydrogenation reactor, condensing the effluent of said hydrogenation reactor to recover one or more organic liquid(s) and an aqueous solution, feeding a non-condensable component of said effluent into an oligomerization reactor; condensing an effluent discharged from the oligomerization reactor to obtain an additional organic liquid and an additional gaseous stream, separating said additional organic liquid, and either combusting said additional gaseous stream to produce heat and electricity, or processing same to obtain recyclable gaseous streams utilizable in said process.

Provided is a selective transfer method including depositing a thin film on a substrate; patterning the thin film using a laser or a tool to acquire a thin film of a target pattern; masking the thin film of the target pattern; selectively controlling a surface wettability through surface treatment of the masked thin film; delaminating the thin film of the target pattern by dipping a surface of the thin film with a wettability changed in response to a completion of the selective surface treatment into a liquid material and by applying a crack opening force capable of delaminating an interface between the thin film and the substrate; and immersing a target substrate into the liquid material when the thin film of the target pattern is floating in the liquid material and then scoop-up transferring the floating thin film of the target pattern.

A unique process and catalyst is described that operates efficiently for the direct production of a high cetane diesel type fuel or diesel type blending stock from stochiometric mixtures of hydrogen and carbon monoxide. This invention allows for, but is not limited to, the economical and efficient production high quality diesel type fuels from small or distributed fuel production plants that have an annual production capacity of less than 10,000 barrels of product per day, by eliminating traditional wax upgrading processes. This catalytic process is ideal for distributed diesel fuel production plants such as gas to liquids production and other applications that require optimized economics based on supporting distributed feedstock resources.

The present invention provides an improved process for removing heat from an exothermic reaction. In particular, the present invention provides a process wherein heat can be removed from multiple reaction trains using a common coolant system.