A rotary sorption bed system includes a rotating sorbent mass of a regenerable sorbent material, in which in a cycle of operation, a given volume of the sorbent mass sequentially passes through first, second, third, and fourth zones, before returning to the first zone. A process fluid stream is directed through the first zone, a regeneration fluid stream is directed through the third zone, and a recycled fluid stream recirculates in a closed loop independent of the process fluid stream and the regeneration fluid stream through the second and fourth zones. At least one parameter of the recycled fluid stream, including at least one of the dry bulb temperature and the dew point of the recycled fluid stream, is monitored and the recycled fluid stream is controlled based on the at least one parameter. The recycled fluid stream can be any one or more of purge, isolation, and purge/regeneration loops.

Provided are apparatus and systems for performing a swing adsorption process. This swing adsorption process may involve performing a startup mode process prior to beginning a normal operation mode process to remove contaminants from a gaseous feed stream. The startup mode process may be utilized for swing adsorption processes, such as TSA and/or PSA, which are utilized to remove one or more contaminants from a gaseous feed stream.

Provided are apparatus and systems for performing a swing adsorption process. This swing adsorption process may involve performing a startup mode process prior to beginning a normal operation mode process to remove contaminants from a gaseous feed stream. The startup mode process may be utilized for swing adsorption processes, such as TSA and/or PSA, which are utilized to remove one or more contaminants from a gaseous feed stream.

The invention relates to a process for the regeneration of an adsorber. For the regeneration a liquid stream (S2) comprising at least one alkane is converted from liquid phase into gaseous phase. Then the adsorber is regenerated and heated by contact with gaseous stream (S2) up to 230 to 270° C. Subsequently, the adsorber is cooled first by contact with gaseous stream (S2) to a temperature of 90 to 150° C. followed by cooling with liquid stream (S2) to a temperature below 80° C. The outflow of the adsorber (S2*) during the cooling with gaseous stream (S2) and optionally the outflow of the adsorber (S2*) during cooling with liquid stream (S2) is recycled in at least one of these steps.

A method of obtaining helium from a helium-containing feed gas. Helium-containing feed gas is fed to a prepurifying unit that uses a pressure swing adsorption process to remove undesirable components from the helium-containing feed gas and obtain a prepurified feed gas. The prepurified feed gas is fed to a membrane unit connected downstream of the prepurifying unit and that has at least one membrane more readily permeable to helium than to at least one further component present in the prepurified feed gas. A pressurized low-helium retentate stream that has not passed through the membrane is fed to the prepurifying unit. The pressurized low-helium retentate is used to displace helium-rich gas from an adsorber that is to be regenerated into an already regenerated adsorber.

An oxygen concentrator is provided with a controller for recovering an oxygen concentration to a level suitable for treatment in a short period of time by selecting an optimum purge time corresponding to the deterioration state of an adsorbent. The 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.

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.

A gas stream is purified by a TSA adsorption scheme including at least two adsorbers following, in an offset manner, a cycle including an adsorption phase, and a subsequently, a regeneration phase. The regeneration phase includes a depressurization step, a pre-regeneration step and a regeneration step. A gas circulator is used to circulate the gas within the adsorber in the pre-regeneration step in a closed loop while the circulating gas is heated with a heater.

Process of treating a net gas stream is disclosed. The process includes sending the net gas stream to a compressor to produce a compressed gas stream. The compressed gas stream is then sent to a pressure swing adsorption unit to produce a hydrogen product stream and a tail gas stream. Tail gas stream from the pressure swing adsorption unit is sent to a first membrane unit to produce a first permeate stream and a first non-permeate stream. Portion of the tail gas stream is sent to a second membrane unit to produce a second permeate stream and a second non-permeate stream.

An inertizing method for the avoidance of fire. An inert or poorly-flammable product gas flow (161) is produced starting from a gas mixture flow (141), which contains one reactive gas and one inert gas. The gas mixture flow (141) is supplied to a gas separation unit (110, 120, 410) under pressure and the reactive gas is at least partially separated from the gas mixture flow (141). Gas components which are not separated are removed as a product gas flow (161) and the reactive gas components separated from the gas mixture flow (141) are removed as a secondary product gas flow (151). The removed product gas flow (161) is introduced into a vortex tube (200) and is separated into a hot product gas partial flow (163) and a cold product gas partial flow (162), and the hot and/or the cold product gas partial flow (162, 163) is introduced into an environment (300).