A process for component separation in a polymer production system, comprising: separating a polymerization product stream into a gas stream and a polymer stream; contacting the polymer stream with a purge gas to yield a purged polymer stream and a spent purge gas stream; introducing the spent purge gas stream to a compressor to produce a compressed gas stream; introducing the compressed gas stream to a first separation unit to produce a first hydrocarbon stream and a membrane unit feed stream; introducing the membrane unit feed stream to a membrane unit to produce a first recovered purge gas stream and a retentate stream; introducing the retentate stream to a second separation unit to produce a second hydrocarbon stream and a PSA unit feed stream; and introducing the PSA unit feed stream to a PSA unit to produce a second recovered purge gas stream and a tail gas stream.

Biogas containing H.sub.2S and CO.sub.2 is upgraded by removing H.sub.2S using PTSA and CO.sub.2 using two stages of gas separation membranes. The first stage permeate may optionally be used a regeneration gas stream. The second stage permeate may optionally be used a cool down gas stream. The PTSA unit includes two or more adsorbent beds each selective for water, VOCs, and H.sub.2S over CO.sub.2 and for H.sub.2S over methane.

A (V)PSA unit for purifying a gas stream by adsorption is provided. The (V)PSA unit comprises, arranged successively in the direction of flow of the feed gas stream, a rotary-structured adsorbent wheel configured so as to drive the gas stream therethrough in an axial manner and allowing the feed gas to dry to a level corresponding to a dew point below 30 C., and an adsorber with a centripetal radial configuration, comprising a bed of particulate adsorbent.

A sorbent bed may comprise a sorbent support comprising at least one of a carbon material, a polymeric material, or alumina, wherein the sorbent support comprises a plurality of pores; and an impregnant configured to absorb ammonia disposed within the plurality of pores in the sorbent support, wherein the sorbent bed comprises between 20% and 60% by weight impregnant.

Systems and methods are provided for using a multi-stage capture process for capture of CO.sub.2 from air. A first or initial sorption process is used to sorb CO.sub.2 from air. After sorption from the air is complete, the desorption step of the initial stage is used to form a secondary CO.sub.2-containing stream that is passed into one or more additional sorption stages. This secondary CO.sub.2-containing stream can be at a concentration of roughly 1.0 vol % or more. Sorption of CO.sub.2 from the secondary CO.sub.2-containing stream is performed using a different contacting method, such as a contacting method that is higher efficiency. The second or later CO.sub.2 sorption stage can produce a CO.sub.2-containing output stream with a CO.sub.2 concentration of 80 vol % or more, or 90 vol % or more, or 95 vol % or more. This high purity output stream can then be sequestered and/or used for further processing.

A system for enhancing adsorption of contaminated vapors to increase treatment capacity of a regenerable, synthetic adsorptive media. The system includes an inlet configured to receive a flow of contaminated vapors. One or more vessels are coupled to the inlet, the one or more vessels each including a regenerable, synthetic adsorptive media therein, are configured to remove contaminants from the vapors by adsorption. A vapor cooling subsystem is coupled to the inlet, and configured to cool the flow of contaminated vapors, thereby increasing the treatment capacity of the regenerable synthetic adsorptive media.

Process and apparatus for producing helium, neon, or argon product gas using an adsorption separation unit having minimal dead end volumes. A second separation unit receives a stream enriched in helium, neon, or argon, and a stream is recycled from the second separation unit back to the adsorption separation unit in a controlled manner to maintain the concentration of the helium, neon, or argon in the feed to the separation unit within a targeted range.

Biogas containing H.sub.2S and CO.sub.2 is upgraded by removing H.sub.2S using PTSA and CO.sub.2 using two stages of gas separation membranes. The first stage permeate may optionally be used a regeneration gas stream. The second stage permeate may optionally be used a cool down gas stream. The PTSA unit includes two or more adsorbent beds each selective for water, VOCs, and H.sub.2S over CO.sub.2 and for H.sub.2S over methane.

Treatment of radioactive waste comprising organic compounds, and sulfur-containing compounds and/or halogen-containing compounds. An apparatus comprises a reaction vessel comprising a filter for carrying out thermal treatment of the waste and a thermal oxidizer. Utilizing co-reactants to reduce gas phase sulfur and halogen from treatment of wastes.

It is an objective of the present invention to provide a gas separation method by which a removal performance to remove a removal object gas component and a recovery rate to recover a recovery object gas component can be satisfied at the same time, and furthermore, a generation efficiency of a product gas can be improved. A raw material gas g0 is fed to one adsorption vessel 11 of an adsorbing device 10 and a permeated gas g1 is sent out. A pressure of the other the adsorption vessels 12 is made lower than a pressure during adsorption and a desorbed gas g2 is sent out. In accordance with an operating cycle of the adsorbing device 10 or according to a condition of the raw material gas g0 or the like, one of the permeated gas g1 and the desorbed gas g2 that has a lower concentration of a priority removal object gas component than the raw material gas g0 is provided as a return gas to the adsorbing device 10, the priority removal object gas component being a gas component to be preferentially removed.