Natural gas liquefaction process in combination with a synthesis gas production process, where the steam derived from the synthesis gas production process is used as a heating source for the implementation of the pre-treatment step for eliminating the impurities liable to freeze during the natural gas liquefaction process.

The invention concerns a process for producing carbon monoxide (CO) from a feed stream comprising carbon dioxide (CO2) and natural gas and/or naphtha the process comprising a syngas generation step, a CO2 removal step and a CO purification step and the process further comprises an SOEC unit which produces CO from a CO2 stream, the process is especially suited for increasing the capacity of existing known CO production plants.

A system and method for processing unconditioned syngas first removes solids and semi-volatile organic compounds (SVOC), then removes volatile organic compounds (VOC), and then removes at least one sulfur containing compound from the syngas. Additional processing may be performed depending on such factors as the source of syngas being processed, the products, byproducts and intermediate products desired to be formed, captured or recycled and environmental considerations.

An integrated process for the production of a useful liquid hydrocarbon product comprises: feeding a gasification zone with an oxygen-containing feed and a first carbonaceous feedstock comprising waste materials and/or biomass, gasifying the first carbonaceous feedstock in the gasification zone to produce first synthesis gas, partially oxidising the first synthesis gas in a partial oxidation zone to generate partially oxidised synthesis gas, combining at least a portion of the first synthesis gas and/or the partially oxidised synthesis gas and at least a portion of electrolysis hydrogen obtained from an electrolyser in an amount to achieve the desired hydrogen to carbon monoxide molar ratio of from about 1.5:1 to about 2.5:1, and to generate a blended synthesis gas, wherein the electrolyser operates using green electricity; and subjecting at least a portion of the blended synthesis gas to a conversion process effective to produce the liquid hydrocarbon product.

In the liquid phase reforming (LPR) of oxygenated C,H-containing compounds such as alcohols, various strategies are disclosed for managing byproduct CO.sub.2. Important processing options include those in which electrolyte, consumed in capturing or precipitating the CO.sub.2 generated from LPR, is regenerated or not regenerated, with carbon emissions potentially being avoided in the latter case. With regeneration, different chemistries are possible, such as in the case of a regeneration cycle utilizing hydroxide anions to precipitate a solid, carbonate form of CO.sub.2 that is generated from reforming. Alternatively, a reaction and regeneration system may use carbonate anions to “capture” CO.sub.2 and thereby maintain it as aqueous, solubilized bicarbonate form.

A system and method for processing unconditioned syngas first removes solids and semi-volatile organic compounds (SVOC), then removes volatile organic compounds (VOC), and then removes at least one sulfur containing compound from the syngas. Additional processing may be performed depending on such factors as the source of syngas being processed, the products, byproducts and intermediate products desired to be formed, captured or recycled and environmental considerations.

A metal/α-MoC.sub.1-x load-type single-atomic dispersion catalyst, a synthesis method therefor, and applications thereof. The catalyst uses α-MoC.sub.1-x as carrier, and has metal that has the mass fraction ranging from 1-100% and that is dispersed on carrier α-MoC.sub.1-x in the single atom form. The catalyst provided in the present application can be adapted to a wide alcohol/water proportion in hydrogen production based on aqueous-phase reforming of alcohols, outstanding hydrogen production performance can be obtained at a variety of proportions, and catalysis performance of the catalyst is much higher than that of metal loaded with an oxide carrier. Especially when the metal is Pt, catalysis performance of the catalyst provided in the present application in the hydrogen production based on aqueous-phase reforming of alcohols is much higher than that of a Pt/α-MoC.sub.1-x load-type catalyst on the α-MoC.sub.1-x carrier on which Pt is disposed on a layer form in the prior art. The hydrogen production performance of the catalyst provided in the present application can be higher than 20,000 h.sup.−1 at the temperature of 190° C.

The invention is directed to a method for heating a process gas in a top or bottom fired reformer, a method for improving the temperature spread over a top or bottom fired reformer, and to a top or bottom fired reformer wherein these methods can applied. This can be achieved by the lane flow rate of at least one outer tube lane being different from the lane flow rate of at least one inner tube lane.

The present invention is directed at the conversion of ammonium nitrate and related compounds upon reaction with methane into compounds such as ethyl acetate, ammonia, nitrogen and hydrogen. The reaction may proceed within a fluid-solid type reactor. The reaction may be facilitated in the presence of inert or catalytic solids.

The invention concerns a process for producing carbon mon-oxide (CO) from a feed stream comprising carbon dioxide (CO2) and natural gas and/or naphtha the process comprising a syngas generation step, a CO2 removal step and a CO purification step and the process further comprises an SOEC unit which produces CO from a CO2 stream, the process is especially suited for increasing the capacity of existing known CO production plants.