A method and apparatus for: providing a ceria aerogel and copper nanoparticle catalyst, flowing a hydrogen, carbon monoxide, and water vapor source gas from an inlet into contact with the catalyst to produce a product gas, and flowing the product gas to an outlet. The concentration of carbon monoxide in the product gas is no more than 50% of the concentration of carbon monoxide in the source gas. The concentration of hydrogen in the product gas is no less than 90% of the concentration of hydrogen in the source gas.

The invention relates to a process for the production of hydrogen-enriched synthesis gas by a catalytic water-gas shift reaction, comprising the steps: introducing a gaseous flow (1) comprising at least one organic sulphide, optionally in its oxide form, in a first reactor (2) comprising a catalyst X.sub.1, collecting a sulfur-containing gaseous flow (3) from the first reactor, introducing the raw synthesis gas (4) in a second reactor (6), introducing the sulfur-containing gaseous flow (3) in the second reactor where the catalytic water-gas shift reaction takes place and comprising a sulfur-resistant shift catalyst X.sub.2, collecting an outlet flow (7) comprising hydrogen-enriched synthesis gas from the second reactor.

The invention also relates to the use of said at least one organic sulphide, optionally in its oxide form, in a process for the production of hydrogen-enriched synthesis gas by a catalytic water-gas shift reaction.

The invention relates to a process for the production of hydrogen-enriched synthesis gas by a catalytic water-gas shift reaction, comprising the steps: introducing a gaseous flow (1) comprising at least one organic sulphide, optionally in its oxide form, in a first reactor (2) comprising a catalyst X.sub.1, collecting a sulfur-containing gaseous flow (3) from the first reactor, introducing the raw synthesis gas (4) in a second reactor (6), introducing the sulfur-containing gaseous flow (3) in the second reactor where the catalytic water-gas shift reaction takes place and comprising a sulfur-resistant shift catalyst X.sub.2, collecting an outlet flow (7) comprising hydrogen-enriched synthesis gas from the second reactor.

The invention also relates to the use of said at least one organic sulphide, optionally in its oxide form, in a process for the production of hydrogen-enriched synthesis gas by a catalytic water-gas shift reaction.

A nanocomposite catalyst includes a support, a multiplicity of nanoscale metal oxide clusters coupled to the support, and one or more metal atoms coupled to each of the nanoscale metal oxide clusters. Fabricating a nanocomposite catalyst includes forming nanoscale metal oxide clusters including a first metal on a support, and depositing one or more metal atoms including a second metal on the nanoscale metal oxide clusters. The nanocomposite catalyst is suitable for catalyzing reactions such as CO oxidation, water-gas-shift, reforming of CO.sub.2 and methanol, and oxidation of natural gas.

A nanocomposite catalyst includes a support, a multiplicity of nanoscale metal oxide clusters coupled to the support, and one or more metal atoms coupled to each of the nanoscale metal oxide clusters. Fabricating a nanocomposite catalyst includes forming nanoscale metal oxide clusters including a first metal on a support, and depositing one or more metal atoms including a second metal on the nanoscale metal oxide clusters. The nanocomposite catalyst is suitable for catalyzing reactions such as CO oxidation, water-gas-shift, reforming of CO.sub.2 and methanol, and oxidation of natural gas.

In a cooled axial flow converter, in which process gas passes from an outer annulus via a catalyst bed, wherein the process gas is converted to a product, to an inner centre tube, the catalyst bed comprises at least one module comprising at least one catalyst layer. Feed means are arranged to provide a flow of process gas from the outer annulus to an inlet part of one or more modules, and collector means are arranged to provide a flow of product stream of converted process gas, which has passed axially down the catalyst bed of one or more of the modules to the centre tube. At least one of the one or more modules comprises one or more cooling plates arranged to be cooled by a cooling fluid.

In a cooled axial flow converter, in which process gas passes from an outer annulus via a catalyst bed, wherein the process gas is converted to a product, to an inner centre tube, the catalyst bed comprises at least one module comprising at least one catalyst layer. Feed means are arranged to provide a flow of process gas from the outer annulus to an inlet part of one or more modules, and collector means are arranged to provide a flow of product stream of converted process gas, which has passed axially down the catalyst bed of one or more of the modules to the centre tube. At least one of the one or more modules comprises one or more cooling plates arranged to be cooled by a cooling fluid.

A carbon capture system includes a hydrogen production module. The hydrogen production module is used to control the amount of hydrogen entering an internal combustion engine to reduce an amount of water vapor generated by the internal combustion engine, thereby increasing the efficiency of the carbon capture device. If too much water vapor is detected in an exhaust of the engine, the amount of hydrogen produced by a hydrogen production module can be increased, thereby reducing the amount of hydrogen entering the engine and reducing the amount of water vapor generated by the engine. A reformer catalyst can be used by the hydrogen production module to remove at least a portion of hydrogen in a fuel stream of the engine.

A carbon capture system includes a hydrogen production module. The hydrogen production module is used to control the amount of hydrogen entering an internal combustion engine to reduce an amount of water vapor generated by the internal combustion engine, thereby increasing the efficiency of the carbon capture device. If too much water vapor is detected in an exhaust of the engine, the amount of hydrogen produced by a hydrogen production module can be increased, thereby reducing the amount of hydrogen entering the engine and reducing the amount of water vapor generated by the engine. A reformer catalyst can be used by the hydrogen production module to remove at least a portion of hydrogen in a fuel stream of the engine.

The present invention concerns a sorption-enhanced water-gas shift (SEWGS) process for the formation of a CO.sub.2 product stream and an H.sub.2 product stream, comprising (a) a reaction step, wherein a feed gas comprising CO.sub.x, wherein x=1-2, and H.sub.2O is fed into a SEWGS reactor containing a catalyst and sorbent material capable of adsorbing CO.sub.2, thereby forming the H.sub.2 product stream and a sorbent material loaded with CO.sub.2; (b) a rinse step, wherein steam is fed to the SEWGS reactor, thereby establishing a pressure in the range of 5-50 bar; (c) a pre-blowdown step, wherein the pressure in the SEWGS reactor is reduced to establish a blowdown pressure in the range of 0.5-1.5 times the partial pressure of CO and CO.sub.2 in the feed gas of step (a); (d) a blowdown step, wherein the pressure in the SEWGS reactor is reduced to the regeneration pressure in the range of 1-5 bar, thereby releasing at least part of the CO.sub.2 from the loaded sorbent material, thereby forming the CO.sub.2 product stream; and (e) a purge step, wherein steam is fed to the SEWGS reactor, thereby releasing further CO.sub.2 molecules from the SEWGS reactor, wherein the off gas released from the reactor during step (c) is collected separately from the CO.sub.2 product stream released from the reactor during step (d). The separate collection of the off gas of pre-blowdown step (c) affords a highly efficient process with excellent CO.sub.2 purity and carbon capture ratio.