A process comprising: subjecting a process gas containing NOx to a stage for absorption of NOx in a suitable absorption means, obtaining nitric acid and a tail gas containing nitrogen, argon and residual NOx; subjecting said tail gas to a treatment which comprises at least one NOx removal stage, obtaining a conditioned tail gas; subjecting at least a portion of said conditioned tail gas to a separation treatment, obtaining a product stream containing argon and a product stream containing nitrogen.

An ammonia decomposition apparatus comprises a casing, a heating zone, a heat exchange zone, a reaction section and a heat exchange coil. The heat exchange coil is spirally wound on an outer wall of the reaction section to efficiently heat ammonia gas. The reaction section has a first reaction zone and a second reaction zone communicated successively, the ammonia gas decomposed into a nitrogen-hydrogen mixture after entering the first reaction zone, with the second reaction zone decomposing for the second time the residual ammonia gas in the nitrogen-hydrogen mixture produced in the first reaction zone, so that the ammonia gas is decomposed more thoroughly. The conversion rate of ammonia gas can reach 99.9% or more, and the residual amount of ammonia gas in the nitrogen-hydrogen mixture can be less than 1000 ppm.

Provided is an oxygen concentrator provided with a control means for recovering an oxygen concentration to a level suitable for treatment in an extremely short period of time by selecting an optimum purge time corresponding to the deterioration state of an adsorbent, wherein judgment of moisture-absorption deterioration is performed when the detected value of the oxygen concentration sensor is equal to or less than a control value of the oxygen concentration in the oxygen-enriched gas and the detected value of the pressure sensor is equal to or more than an adsorption pressure at which the oxygen concentration increases significantly before and after the control to reduce the purge time, and control of reducing a time for the purge step shorter than a preset time is performed.

In a method for separating argon by cryogenic distillation, in which a flow containing argon, oxygen and nitrogen and being more rich in argon than the air is sent to a distillation column, and an argon-rich gas flow is withdrawn at the top of the column, a portion of the argon-rich gas flow is mixed with beads to form a gas mixture containing beads, the beads being capable of adsorbing oxygen in the presence of argon at the column operating temperatures; the portion of the argon-rich gas flow mixed with the beads is condensed and then sent to the top of the column; and a bottom liquid containing beads is withdrawn from the column and treated to remove the beads, the beads removed being regenerated to remove the adsorbed oxygen and being again mixed with the argon-rich gas flow.

Processes and systems for the energy efficient capture of CO.sub.2 from a flue gas stream such as produced or resulting from power plant operation, are provided. The processes and systems integrate the use of high CO.sub.2/N.sub.2 selectivity membranes and high CO.sub.2 flux membranes, to capture CO.sub.2. Useful membranes can desirably be graphene oxide-based membranes.

Disclosed is an oxygen generator with improved noise and vibration reduction, compactness, and user convenience. The oxygen generator includes a gas separation membrane module including: gas separation membranes formed of a bundle of hollow fiber membranes; an atmospheric air inlet, to one end of which one end of the gas separation membranes is bonded, sealed, and attached, and the other end of which air in the atmosphere enters; a nitrogen outlet, to one end of which the other end of the gas separation membranes is bonded, sealed, and attached, and the other end of which nitrogen exits; a guide rail where the gas separation membranes are wound in a coil and stored on an inner surface thereof; a gas separation membrane module casing containing the guide rail where the gas separation membranes are stored.

In a helium purification process, a stream containing at least 10% of helium, at least 10% of nitrogen in addition to hydrogen and methane is separated to form a helium-enriched stream containing hydrogen, a first stream enriched in nitrogen and in methane and a second stream enriched in nitrogen and in methane, the helium-enriched stream is treated to produce a helium-rich product and a residual gas containing water, the residual gas is treated by adsorption (TSA) to remove the water and the regeneration gas from the adsorption is sent to a combustion unit (O).

A process for producing ammonia make-up synthesis gas and a procedure for revamping a front-end of an ammonia plant for producing ammonia make-up synthesis gas are disclosed, wherein the make-up synthesis gas is produced by means of steam reforming of a hydrocarbon gaseous feedstock; said front-end includes a primary reformer, a secondary reformer, a shift conversion section, a CO2 removal section and optionally a methanation section; a shell-and-tube gas-heated reformer is installed after said secondary reformer, and a portion of the available feedstock is reformed in the tubes of said gas-heated reformer, and heat is provided to the shell side of said gas-heated reformer by at least a portion of product gas leaving the secondary reformer, possibly mixed with product gas leaving the tubes of said gas-heated reformer.

An ammonia decomposition apparatus comprises a casing, a heating zone, a heat exchange zone, a reaction section and a heat exchange coil. The heat exchange coil is spirally wound on an outer wall of the reaction section to efficiently heat ammonia gas. The reaction section has a first reaction zone and a second reaction zone communicated successively, the ammonia gas decomposed into a nitrogen-hydrogen mixture after entering the first reaction zone, with the second reaction zone decomposing for the second time the residual ammonia gas in the nitrogen-hydrogen mixture produced in the first reaction zone, so that the ammonia gas is decomposed more thoroughly. The conversion rate of ammonia gas can reach 99.9% or more, and the residual amount of ammonia gas in the nitrogen-hydrogen mixture can be less than 1000 ppm.

In a helium purification process, a stream containing at least 10% of helium, at least 10% of nitrogen in addition to hydrogen and methane is separated to form a helium-enriched stream containing hydrogen, a first stream enriched in nitrogen and in methane and a second stream enriched in nitrogen and in methane, the helium-enriched stream is treated to produce a helium-rich product and a residual gas containing water, the residual gas is treated by adsorption (TSA) to remove the water and the regeneration gas from the adsorption is sent to a combustion unit (O).