The invention relates to a cyclic method of producing a hydrogen rich and/or a carbon monoxide rich stream using different materials, a first solid material, a second solid material and a CO.sub.2 sorbent material.

In a first step a first gas stream comprising steam and at least one reductant is brought in contact with the three materials resulting in a hydrogen rich outlet stream.

In a second step, the captured CO.sub.2 from the first step is released and converted to CO to produce a CO rich outlet stream.

The invention further relates to an installation for producing a hydrogen rich and/or carbon monoxide rich stream.

The invention relates to a cyclic method of producing a hydrogen rich and/or a carbon monoxide rich stream using different materials, a first solid material, a second solid material and a CO.sub.2 sorbent material.

In a first step a first gas stream comprising steam and at least one reductant is brought in contact with the three materials resulting in a hydrogen rich outlet stream.

In a second step, the captured CO.sub.2 from the first step is released and converted to CO to produce a CO rich outlet stream.

The invention further relates to an installation for producing a hydrogen rich and/or carbon monoxide rich stream.

The present disclosure relates to a novel improved method for continuous crystallization of highly crystalline clathrate hydrates. The novel improved method utilizes a novel hydrator capable of overcoming heat and mass transfer limitations that usually constrain crystallization rate and thus reduces process productivity. The disclosed method and hydrator are for production of crystalline clathrates in general, CO.sub.2 capture, capture of other clathrate forming compounds, CO.sub.2 storage and transportation, storage and transportation of any clathrate forming compound in a solid lattice, gas separation or water desalination or purification purposes.

The present disclosure relates to a novel improved method for continuous crystallization of highly crystalline clathrate hydrates. The novel improved method utilizes a novel hydrator capable of overcoming heat and mass transfer limitations that usually constrain crystallization rate and thus reduces process productivity. The disclosed method and hydrator are for production of crystalline clathrates in general, CO.sub.2 capture, capture of other clathrate forming compounds, CO.sub.2 storage and transportation, storage and transportation of any clathrate forming compound in a solid lattice, gas separation or water desalination or purification purposes.

A quaternary ammonium-functionalized poly(arylene ether sulfone) copolymer for moisture-swing CO2 capture, and a method for producing the same, is disclosed. The copolymer includes a polysulfone copolymer having a copolymerization unit based on diallyl bisphenal A (DABA) and has quaternary ammonium functionalities. The method for preparation of a quaternary ammonium-functionalized poly(arylene ether sulfone) copolymer includes reacting diallyl bisphenol A (DABA) with bisphenol A (BPA) and 4,4'-difluorodiphenyl sulfone (DFDPS) to form an allyl-modified poly(arylene ether sulfone) (PAES-co-APAES) copolymer, then modifying the PAES-co-APAES copolymer to convert the allyl functionalities to tertiary amines, forming tertiary amine-modified PAES (PAES-co-TAPAES) copolymer. The method also includes converting the tertiary amine of the PAES-co-TAPAES copolymer to quaternary ammonium, forming quaternary ammonium-modified PAES. These quaternary ammonium-modified PAES may be processed into membranes, films, and hollow fibers.

A quaternary ammonium-functionalized poly(arylene ether sulfone) copolymer for moisture-swing CO2 capture, and a method for producing the same, is disclosed. The copolymer includes a polysulfone copolymer having a copolymerization unit based on diallyl bisphenal A (DABA) and has quaternary ammonium functionalities. The method for preparation of a quaternary ammonium-functionalized poly(arylene ether sulfone) copolymer includes reacting diallyl bisphenol A (DABA) with bisphenol A (BPA) and 4,4'-difluorodiphenyl sulfone (DFDPS) to form an allyl-modified poly(arylene ether sulfone) (PAES-co-APAES) copolymer, then modifying the PAES-co-APAES copolymer to convert the allyl functionalities to tertiary amines, forming tertiary amine-modified PAES (PAES-co-TAPAES) copolymer. The method also includes converting the tertiary amine of the PAES-co-TAPAES copolymer to quaternary ammonium, forming quaternary ammonium-modified PAES. These quaternary ammonium-modified PAES may be processed into membranes, films, and hollow fibers.

Methods and systems to achieve clean fuel processing systems in which carbon dioxide emissions (1) from sources (2) may be processed in at least one processing reactor (4) containing a plurality of chemoautotrophic bacteria (5) which can convert the carbon dioxide emissions into biomass (6) which may then be used for various products (21) such as biofuels, fertilizer, feedstock, or the like. Sulfate reducing bacteria (13) may be used to supply sulfur containing compounds to the chemoautotrophic bacteria (5).

Methods and systems to achieve clean fuel processing systems in which carbon dioxide emissions (1) from sources (2) may be processed in at least one processing reactor (4) containing a plurality of chemoautotrophic bacteria (5) which can convert the carbon dioxide emissions into biomass (6) which may then be used for various products (21) such as biofuels, fertilizer, feedstock, or the like. Sulfate reducing bacteria (13) may be used to supply sulfur containing compounds to the chemoautotrophic bacteria (5).

A sulfur trap provides separation of elemental molten sulfur from a process stream comprising a mixture of sulfur and associated tail-gases. The sulfur trap comprises a vertically-oriented cylindrical wall having a chamber for receiving the process stream, a float positioned in the chamber, the float attached to a float end of a lever, a nozzle insert attached to the distal end of the lever, and a lever fulcrum positioned intermediate the lever float end and the lever nozzle insert end. The float, lever, nozzle insert and outlet are constructed to allow the float position to control nozzle insert engagement of the outlet, particularly to close the outlet when the float is elevated by molten sulfur and to disengage from the outlet to allow discharge flow of liquid sulfur at a determined level of sulfur within the chamber. Embodiments of a method of separating liquid sulfur from gases are also provided.

A method for decomposing a nitroso compound, comprising: adding an aqueous solution containing hydrogen halide to a liquid to be treated that contains the nitroso compound in such a manner that the hydrogen halide is present in an amount of 2 mol or more and 20 mol or less per mol of a nitroso group in the nitroso compound; and subsequently heating the resulting liquid to be treated at a temperature of not lower that 75° C. and not higher than a boiling point of water under ordinary pressure, thereby an amines are recovered.