A method and to a device for producing a synthesis gas, which contains carbon monoxide and hydrogen, wherein natural gas having a first carbon dioxide partial pressure (CO.sub.2 pressure) is provided and is processed inter alia by means of a pressure increase to form a natural gas input for a thermochemical conversion, in which a synthesis raw gas having a second CO.sub.2 pressure greater than the first CO.sub.2 pressure is produced, from which synthesis raw gas at least carbon dioxide is subsequently separated in order to obtain the synthesis gas and carbon dioxide, at least some of which is returned and is used in the thermochemical conversion of the natural gas input. To separate carbon dioxide, the synthesis raw gas is conducted across the one membrane on the retentate side, which membrane is permeable to carbon dioxide and is flushed on the permeate side by the provided natural gas.

A process for producing methanol including the following steps: (a) reacting, via a catalytic partial oxidation (CPO) reaction, a CPO reactant mixture (hydrocarbons, oxygen, and optionally steam) in a CPO reactor to produce syngas; wherein the CPO reactor has a CPO catalyst; and wherein the syngas includes hydrogen, carbon monoxide, carbon dioxide, water, and unreacted hydrocarbons; (b) introducing the syngas to a methanol reactor to produce a methanol reactor effluent stream; wherein the methanol reactor effluent stream includes methanol, water, hydrogen, carbon monoxide, carbon dioxide, and hydrocarbons; and (c) separating the methanol reactor effluent stream into a crude methanol stream and a vapor stream. The crude methanol stream comprises includes methanol and water. The vapor stream includes hydrogen, carbon monoxide, carbon dioxide, and hydrocarbons; and wherein the crude methanol stream has water in an amount of less than about 10 wt. %, based on the total weight of the crude methanol stream.

A hydrogen feed stream comprising oxygen and one or more impurities selected from the group consisting of nitrogen, argon, methane, carbon monoxide, carbon dioxide, and water, is purified using a cryogenic temperature swing adsorption (CTSA) process with high overall recovery of hydrogen. The CTSA is regenerated using an inert gas to prevent an explosive mixture of hydrogen and oxygen from occurring.

A method of producing hydrogen using biomass includes: pretreating the biomass using an ionic liquid; and extracting hydrogen by reacting the pretreated biomass with an alkaline substance.

The invention relates to a catalytic process for upgrading a renewable crude oil produced from biomass and/or waste comprising providing a renewable crude oil and pressurizing it to a pressure in the range in the range 60 to 150 bar, contacting the pressurized renewable crude oil with hydrogen and at least one heterogeneous catalyst contained in a first reaction zone at a weight based hourly space velocity (WHSV) in the range 0.1 to 2.0 h.sub.−1 and at a temperature in the range of 150° C. to 360° C., hereby providing a partially upgraded renewable crude oil, separating the partially upgraded renewable crude oil from the first reaction zone to a partially upgraded heavy renewable oil fraction, a partially upgraded light renewable oil fraction, a water stream and a process gas stream, introducing the separated and partially upgraded heavy renewable oil fraction and separated process gas to a second reaction zone comprising at least two reactors arranged in parallel and being adapted to operate in a first and a second mode of operation, the reactors comprising dual functioning heterogeneous catalyst(-s) capable of performing a catalytic steam cracking reaction in a first mode of operation or a steam reforming reaction in a second mode of operation, where the partially upgraded heavy renewable oil fraction from the first reaction zone is contacted with the dual functioning heterogeneous catalyst and steam at a pressure of 10 to 150 bar and a temperature of 350° C. to 430° C. whereby a catalytic steam cracking of the partially upgraded heavy renewable oil is performed in the reactors in the first mode of operation, hereby providing a further upgraded heavy renewable oil fraction, while separated process gas from the first and/or second reaction zone is contacted with the dual functioning catalyst and steam at a pressure of 0.1 to 10 bar and a temperature of 350 to 600° C. in the reactors in the second mode of operation and contacted with the dual functioning catalyst, thereby producing a hydrogen enriched gas, separating the further upgraded heavy renewable oil fraction from the catalytically steam cracking reactor to at least one light renewable oil fraction, a heavy renewable oil fraction, a hydrogen rich process gas and a water phase, separating hydrogen from the hydrogen enriched gas from the catalytic steam cracking zone and/or from the catalytic steam reforming and recycling it to the first reaction zone, alternating the reactors between the first mode of operation and the second mode of operation at predetermined time intervals thereby allowing for regeneration of the heterogeneous catalyst for the catalytic steam cracking in the first mode of op

Methods and systems for gas separation of syngas applying differences in water solubilities of syngas components, the method including producing a product gas comprising hydrogen and carbon dioxide from a hydrocarbon fuel source; separating hydrogen from the product gas to create a hydrogen product stream and a byproduct stream by solubilizing components in water that are more soluble in water than hydrogen; injecting the byproduct stream into a reservoir containing mafic rock; and allowing components of the byproduct stream to react in situ with components of the mafic rock to precipitate and store components of the byproduct stream in the reservoir.

A process for the manufacture of a useful product from synthesis gas having a desired hydrogen to carbon monoxide molar ratio comprises gasifying a first carbonaceous feedstock comprising waste materials and/or biomass in a gasification zone to produce a first synthesis gas; optionally partially oxidising the first synthesis gas in a partial oxidation zone to generate oxidised synthesis gas; reforming a second carbonaceous feedstock to produce a second synthesis gas, the second synthesis gas having a different hydrogen to carbon ratio from that of the first raw synthesis gas; combining at least a portion of the first synthesis gas and at least a portion of the second synthesis gas in an amount to achieve the desired hydrogen to carbon molar ratio and to generate a combined synthesis gas and subjecting at least part of the combined synthesis gas to a conversion process effective to produce the useful product.

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 process for preparing methanol from a carbon-containing feedstock by producing synthesis gas therefrom in a synthesis gas production unit, converting the synthesis gas to methanol in a methanol synthesis unit and working up the reaction mixture obtained stepwise to isolate the methanol, wherein the carbon monoxide, carbon dioxide, dimethyl ether and methane components of value from the streams separated off in the isolation of the methanol are combusted with an oxygenous gas, and the carbon dioxide in the resultant flue gas is separated off in a carbon dioxide recovery unit and recycled to the synthesis gas production unit and/or to the methanol synthesis unit.

A plant and process for producing a hydrogen rich gas are provided, said process comprising the steps of: reforming a hydrocarbon feed in an autothermal reformer thereby obtaining a syngas; shifting said syngas in a shift configuration including a high temperature shift step; removal of CO.sub.2 in a CO.sub.2-removal section by amine wash thereby forming a hydrogen rich stream, a portion of which is used as low carbon hydrogen fuel, as well as a CO.sub.2-rich gas and a high-pressure flash gas stream. The high-pressure flash gas stream is advantageously integrated into the plant and process for further improving carbon capture.