A carbon capture system can include a plurality of CO.sub.2 thermal swing adsorption (TSA) beds. The plurality of CO.sub.2 TSA beds can include at least a first TSA bed, a second TSA bed, and a third TSA bed configured to capture CO.sub.2 within a capture temperature range and to regenerate the captured CO.sub.2 at a regeneration temperature range above the capture temperature range. The carbon capture system can include a plurality of valves and associated flow paths configured to allow switching operational modes of each of the first, second, and third TSA beds.

A carbon capture system can include a plurality of CO.sub.2 thermal swing adsorption (TSA) beds. The plurality of CO.sub.2 TSA beds can include at least a first TSA bed, a second TSA bed, and a third TSA bed configured to capture CO.sub.2 within a capture temperature range and to regenerate the captured CO.sub.2 at a regeneration temperature range above the capture temperature range. The carbon capture system can include a plurality of valves and associated flow paths configured to allow switching operational modes of each of the first, second, and third TSA beds.

A hydrogen production apparatus including a desulfurizer, a reformer, a CO transformer a gas flow path, and a purge gas supply path which is provided where a purge gas is supplied to an upstream side of a pressure feeding apparatus in the gas flow path, prior to a stopping operation, a purging step of replacing gas within the gas flow path with the purge gas and filling the purge gas into the gas flow path is performed, and in a start-up operation in which a heating means is operated to increase the temperature of the gas within the gas flow path, which is performed prior to a hydrogen purification operation, a pressure increasing step of supplying the purge gas from the purge gas supply path to the closed circulation circuit and increasing the pressure within the closed circulation circuit is performed.

Provided is a method for concentrating ozone gas, including the steps of: allowing ozone gas to be adsorbed onto an adsorbent in a first adsorption vessel; reducing pressure in a concentration vessel in a state where the concentration vessel does not communicate with the first adsorption vessel; discharging part of gas in the first adsorption vessel; introducing first concentrated mixed gas in the concentration vessel by desorbing ozone gas in the first concentrated mixed gas and delivering the desorbed ozone gas into the concentration vessel; allowing ozone gas to be adsorbed onto an adsorbent in a second adsorption vessel; and introducing second concentrated mixed gas into the concentration vessel in a state where the concentration vessel into which the first concentrated mixed gas is introduced and the second adsorption vessel that houses an adsorbent. Also provided is an apparatus for concentrating ozone gas for implementing the method.

Provided is method for concentrating ozone gas the method including the steps of: allowing ozone gas to be adsorbed onto the adsorbent by introducing ozone gas-containing raw material mixed gas into an adsorption vessel (20) that houses an adsorbent for adsorbing ozone gas; reducing a pressure in a concentration vessel (30) in a state where the concentration vessel (30) does not communicate with the adsorption vessel (20), the concentration vessel (30) being configured to be connected to the adsorption vessel (20) so as to be interswitchable between a state where the concentration vessel (30) communicates with the adsorption vessel (20) and a state where the concentration vessel does not communicate with the adsorption vessel (20); and introducing concentrated mixed gas including ozone gas with a higher ozone gas concentration than the ozone gas concentration in the raw material mixed gas into the concentration vessel (30) by desorbing the ozone gas adsorbed onto the adsorbent using a pressure difference between the internal pressure of the concentration vessel (30) and an internal pressure of the adsorption vessel (20) in a state where the concentration vessel (30) having a reduced internal pressure communicates with the adsorption vessel (20) that houses the adsorbent onto which the ozone gas is adsorbed, and delivering the desorbed ozone gas into the concentration vessel (30). Also provided is an apparatus (1) for concentrating ozone gas for implementing the method.

An integrated fuel combustion system with gas separation (adsorptive, absorptive, membrane or other suitable gas separation) separates a portion of carbon dioxide from a combustion gas mixture and provides for recycle of separated carbon dioxide to the intake of a fuel combustor for combustion. A process for carbon dioxide separation and recycle includes: admitting combustion gas to an adsorptive gas separation system contactor containing adsorbent material; adsorbing a portion of carbon dioxide; recovering a first product stream depleted in carbon dioxide for release or use; desorbing carbon dioxide from the adsorbent material and recovering a desorbed second product stream enriched in carbon dioxide for sequestration or use; admitting a conditioning and/or desorption fluid into the contactor and desorbing a second portion of carbon dioxide to recover a carbon dioxide enriched conditioning stream; and recycling a portion of the carbon dioxide enriched conditioning stream to an inlet of fuel combustor to pass through the fuel combustor for combustion.

A three-product PSA system which produces three product streams from a feed gas mixture comprising a light key component, at least one heavy key component, and at least one intermediate key component is described. The three-product PSA system produces a high pressure product stream enriched in the light key component, a low pressure tail gas stream enriched in the at least one heavy key component, and an intermediate pressure vent gas stream enriched in the at least one intermediate key component.

A pressure swing adsorption (PSA) system for purifying a feed gas is provided. The PSA system may have a first adsorber bed and a second adsorber bed, each having a feed port, a product port, and adsorbent material designed to adsorb one or more impurities from the feed gas to produce a product gas. The PSA system may also have a first valve configured to direct flows of the feed gas and the product gas through a network of piping. The PSA system may further have a first orifice configured to regulate a flow rate of gas between the first adsorber bed and the second adsorber bed during the pressure equalization step and a second orifice configured to regulate a flow rate of gas between the first adsorber bed and the second adsorber bed during the purge step.

A temperature swing adsorption (TSA) process for removing a target component from a gaseous mixture (111), said process being carried out in a plurality of reactors (101, 102, 103), wherein each reactor (101) performs the following steps: an adsorption step (a) wherein an input stream (111) of said gaseous mixture is contacted with a solid adsorbent selective for said target component, producing a first waste stream (112) depleted of the target component; a heating step (b) for regeneration of the loaded adsorbent providing a first output stream (115) containing the target component; a cooling step (c) of the regenerated adsorbent, said TSA process also comprising: i) a pre-cooling step (b1) before said cooling step (c), wherein the regenerated adsorbent is contacted with a waste stream (137) which is produced by the adsorption step (a) of another reactor (103) and a second output stream (116) of the target component is produced; ii) a pre-heating step (a1) after said adsorption step (a) and before said heating step (b), wherein the loaded adsorbent is contacted with a rinse stream (126) which is produced by the pre-cooling step of another reactor (102).

A fuel vapor processing apparatus may include a first adsorption chamber, a second adsorption chamber and a third adsorption chamber that are arranged in series with respect to a flow of gas. A ratio of a length to a diameter of the second adsorption chamber may be larger than a ratio of a length to a diameter of the first adsorption chamber. A filling ratio of an adsorbent within the second adsorption chamber may be smaller than a filling ratio of an adsorbent within the first adsorption chamber.