A photocatalyst suspension reactor for solar fuel formation. The reactor may comprise a shallow pool filled with a first portion of an electrolyte solution. The electrolyte solution may comprise a solvent, a plurality of redox shuttle molecules, and a plurality of photocatalyst particles. The reactor may further comprise a plurality of tubes disposed on a surface of the shallow pool, each tube of the plurality of tubes comprising an upper half and a lower half. The upper half may comprise a transparent material configured to be minimally permeable to hydrogen gas and oxygen gas. The lower half may be configured to be filled with a second portion of the electrolyte solution and comprises an ion bridge material permeable to the plurality of redox shuttle molecules and minimally permeable to the plurality of photocatalyst particles.

The present invention provides for a pressure swing adsorption (PSA) process for the substantial removal of H.sub.2O and CO.sub.2 from a synthesis gas to obtain a multicomponent product gas substantially free of H.sub.2O and CO.sub.2 with high recovery of the product gas. Further, the present invention provides an integrated process that achieves sufficiently high H.sub.2 and CO recoveries such that compression and recycling of the syngas purification PSA tailgas is not necessary to be economically advantageous compared to the conventional processes.

The invention relates to a system for separating and storing molecules, atoms and/or ions from air, wherein at least one air collecting means comprises at least one collecting tank configured to receive molecules, atoms and/or ions separated from air through an inlet and at least one membrane adapted to fit in the inlet of the collecting tank and configured to let a specified pre-determined size of molecules, atoms and/or ions to pass through the at least one membrane. The system further comprises at least one storing tank for storing the separated molecules, atoms and/or ions, and at least one outlet. The system according to the invention can be used to utilize the energy present in such molecules or separate unwanted gases present in the air.

Provided are a hydrogen recycle system and a hydrogen recycle method, whereby hydrogen can be purified to high purity at high yield from a gas, said gas being exhausted from a nitride compound production device, and recycled. The hydrogen recycle system comprises an exhaust gas supply path supplying a gas exhausted from a nitride compound production device, a hydrogen recycle means and a hydrogen supply path. The hydrogen recycle means of the hydrogen recycle system is characterized by comprising: a plasma reaction vessel that defines at least a part of a discharge space; a hydrogen separation membrane that divides the discharge space from a hydrogen flow path communicated with the hydrogen supply path, defines at least a part of the discharge space by one surface thereof and also defines at least a part of the hydrogen flow path by the other surface thereof; an electrode that is disposed outside the discharge space; and an adsorbent that is filled in the discharge space and adsorbs the supplied exhaust gas.

A reactor for converting hydrogen sulfide into hydrogen gas and sulfur.

The invention includes a gas processing system for transforming a hydrocarbon-containing inflow gas into outflow gas products, where the system includes a gas delivery subsystem, a plasma reaction chamber, and a microwave subsystem, with the gas delivery subsystem in fluid communication with the plasma reaction chamber, so that the gas delivery subsystem directs the hydrocarbon-containing inflow gas into the plasma reaction chamber, and the microwave subsystem directs microwave energy into the plasma reaction chamber to energize the hydrocarbon-containing inflow gas, thereby forming a plasma in the plasma reaction chamber, which plasma effects the transformation of a hydrocarbon in the hydrocarbon-containing inflow gas into the outflow gas products, which comprise acetylene and hydrogen. The invention also includes methods for the use of this gas processing system.

Bifunctional catalyst compositions, methods, and systems are provided for the use of CO.sub.2 as a soft oxidizing agent to effectively convert low-value small alkanes to high-value small olefins. The bifunctional catalyst comprises a metal oxide catalyst and a redox-active ceramic support.

Processes for producing a hydrogen-enriched gas stream are described. A hydrocarbon containing feed is processed in a hydrogen production process unit, and the synthesis gas formed is subjected to a water gas shift reaction. The shifted synthesis gas is sent for processing to recover hydrogen and carbon dioxide. The hydrogen and carbon dioxide recovery processes involve separating a purified hydrogen product stream and a purified carbon dioxide stream from the shifted synthesis stream and recycling synthesis gas to the reforming feed after recovery of CO.sub.2 and H.sub.2, thereby avoiding carbon slip from the process and lowering the overall carbon intensity.

A stripper off gas stream from a low pressure hydroprocessing unit may be routed to a hydrogen recovery unit to recover hydrogen. The stripper off gas stream may be scrubbed of acid gases and then compressed to hydrogen recovery pressure before it is subjected to hydrogen recovery such as in a pressure swing adsorption unit to recover high purity hydrogen.

Proposed are a process and a plant for producing a synthesis gas product stream having an adjustable H.sub.2/CO ratio and a pure hydrogen stream, wherein it is provided according to the invention that a substream of a deacidified synthesis gas stream is supplied to a membrane separation plant fitted with a hydrogen-selective membrane and the remaining substream is supplied to a pressure swing adsorption plant, wherein the latter affords a pure hydrogen stream and a fuel gas stream. The hydrogen-enriched permeate stream obtained from the membrane separation is likewise supplied to the pressure swing adsorption plant, thus enhancing the yield of pure hydrogen. The hydrogen-depleted retentate stream obtained from the membrane separation is discharged as a synthesis gas product stream and if of a suitable composition may be utilized as oxo gas.