A mixed gas separation method includes supplying a mixed gas containing at least N.sub.2, H.sub.2, and CO.sub.2 and having a CO.sub.2 concentration of 30% or less by volume to a first separation membrane that selectively allows passage of H.sub.2, supplying the first non-permeated gas to a second separation membrane that selectively allows passage of CO.sub.2, and supplying the second non-permeated gas to a CO.sub.2 collector that separates and collects CO.sub.2 by a separation method other than membrane separation to collect CO.sub.2 contained in the second non-permeated gas. The first non-permeated gas has a CO.sub.2 concentration that is 5% or more by volume higher than or equal to the CO.sub.2 concentration in the mixed gas. The second non-permeated gas has an N.sub.2 concentration of 50% or more by volume and an H.sub.2 concentration of 30% or less by volume.

A boil-off management system for a cryotank includes a boil-off conduit which is fluidically connectable to a cryotank via a boil-off valve. The boil-off management system further includes an air feed conduit and a mixing chamber for mixing a first medium (e.g., hydrogen) flowing in through the boil-off conduit with a second medium (e.g., air and/or oxygen) flowing in through the air feed conduit. A catalytic converter is arranged downstream of the mixing chamber and an outlet downstream of the catalytic converter. At least one enrichment apparatus is provided and configured to temporarily increase the proportion of the first medium flowing in through the boil-off conduit in relation to the second medium flowing in through the air feed conduit at the catalytic converter.

Disclosed is an apparatus for producing a hydrogen gas according to the present disclosure includes a desulfurizer, a plasma reactor, a first adsorber, and a heat exchanger. The disclosed apparatus does not require additional purification of hydrogen and has excellent energy efficiency by utilizing wasted heat of the produced hydrogen.

A method for separating a gas mixture flow, n which uses a temperature-change adsorption plant having a number of adsorption units which are operated in a first and a second operating mode. The first operating mode comprises guiding a gas mixture flow at least in part through an adsorption chamber of an adsorption unit and subjecting this flow to an adsorptive exchange with at least one adsorbent. The second operating mode comprises guiding a first heat transfer fluid flow at a first temperature through a heat-exchange arrangement of an adsorption unit. The first operating mode also comprises guiding a second heat transfer fluid flow at a second temperature through the heat-exchange arrangement of the respective adsorption unit. The adsorption units are operated in a third operating mode which comprises guiding a third heat transfer fluid flow at a third temperature through the heat-exchange arrangement of the respective adsorption unit.

The present invention discloses methods for extracting and recycling ammonia in MOCVD processes by FTrPSA. Through pretreatment, medium-shallow temperature PSA concentration, condensation and freezing, liquid ammonia vaporization, PSA ammonia extraction, and ammonia gas purification procedures, ammonia-containing exhaust gases from MOCVD processes are purified to meet the electronic-level ammonia gas standard required by the MOCVD processes, so as to implement recycling and reuse of the exhaust gases, where the ammonia gas yield is greater than or equal to 70-85%. The present invention solves the technical problem that atmospheric-pressure or low-pressure ammonia-containing exhaust gases in MOCVD processes cannot be returned to the MOCVD processes for use after being recycled, and fills the gap in green and circular economy development of the LED industry.

The invention provides for the optimal utilization of gas by a fermentation process, whereby the various components within the gas stream are separated to increase the efficiency of the microorganisms. The invention is capable of tailoring the composition of the gas being used by the fermentation process so as to enhance the production of various products. The invention is capable of applying such controlled separation and utilization of gas to produce different products in two parallel fermentation processes. The invention is also capable of applying such controlled separation and utilization of gas to produce one product in a first fermentation process, which may be converted to a different product in a second fermentation process. The invention is additionally capable of mitigating culture inhibition.

An electrochemical cell active hydrogen capture and release system including a first zone having a target predetermined concentration of hydrogen c1 and housing: an electrical component, an adsorbing electrode including a hydrogen adsorbing material, a counter electrode separated from the adsorbing electrode, and an electric circuit connecting the adsorbing and counter electrodes to apply electrical bias configured to facilitate capture and release of hydrogen gas from the adsorbing electrode; and a second zone having a target predetermined concentration of hydrogen c2, c2 being greater than c1.

A system and method of pre-purification of a feed gas stream is provided that is particularly suitable for pre-purification of a feed air stream in cryogenic air separation unit. The disclosed pre-purification systems and methods are configured to remove substantially all of the hydrogen, carbon monoxide, water, and carbon dioxide impurities from a feed air stream and is particularly suitable for use in a high purity or ultra-high purity nitrogen plant. The pre-purification systems and methods preferably employ two or more separate layers of hopcalite catalyst with the successive layers of the hopcalite separated by a zeolite adsorbent layer that removes water and carbon dioxide produced in the hopcalite layers. The separate layers of hopcalite catalyst preferably have different volumes and/or different average particle sizes of the hopcalite materials.

A method of forming a carbon molecular sieve membrane includes dissolving a halogenated precursor polymer in a solvent, thereby forming a dissolved halogenated precursor polymer. Homogeneously dehydrohalogenating the dissolved halogenated precursor polymer with an organic amine base to form a partially dehydrohalogenated polymer. Forming a thin film from the partially dehydrohalogenated polymer. Pyrolyzing the thin film to form the carbon molecular sieve membrane.

A system comprising a pumping system configured to pump respective exhaust gases from each of a plurality of chemical etching process chambers and to combine the exhaust gases to provide a combined exhaust gas, and a noble gas recovery system configured to process the combined exhaust gas to remove one or more noble gases therefrom.