Provided are apparatus and systems for performing a swing adsorption process. This swing adsorption process may involve passing an input feed stream through two swing adsorption systems as a purge stream to remove contaminants, such as water, from the respective adsorbent bed units. The wet purge product stream is passed to a solvent based gas treating system, which forms a wet hydrocarbon rich stream and a wet acid gas stream. Then, the wet hydrocarbon rich stream and the wet acid gas stream are passed through one of the respective swing adsorption systems to remove some of the moisture from the respective wet streams.

A device for the electrochemical production of a product containing CO, and a method for the electrochemical production of a product containing CO, in which a return of a material stream containing the educt and CO is carried out after the electrochemical production.

A carbonized PVDC copolymer useful for the separation of an olefin from its corresponding paraffin may be made by heating a polyvinylidene chloride copolymer film or hollow fiber having a thickness of 1 micrometer to 20 micrometers to a pretreatment temperature of 100° C. to 180° C. to form a pretreated polyvinylidene chloride copolymer film and then heating the pretreated polyvinylidene chloride copolymer film to a maximum pyrolysis temperature from 350° C. to 750° C. A process for separating an olefin from its corresponding paraffin in a gas mixture is comprised of flowing the gas mixture through the aforementioned carbonized polyvinylidene chloride (PVDC) copolymer to produce a permeate first stream having an increased concentration of the olefin and a second retentate stream having an increased concentration of its corresponding paraffin.

A process for separating hydrogen from a gas mixture having hydrogen and a larger gas molecule is comprised of flowing the gas mixture through a carbonized polyvinylidene chloride (PVDC) copolymer membrane having a hydrogen permeance in combination with a hydrogen/methane selectivity, wherein the combination of hydrogen permeance and hydrogen/methane selectivity is (i) at least 30 GPU hydrogen permeance and at least 200 hydrogen/methane selectivity or (ii) at least 10 GPU hydrogen permeance and at least 700 hydrogen/methane selectivity. The carbonized PVDC copolymer may be made by heating and restraining a polyvinylidene chloride copolymer film or hollow fiber having a thickness of 1 micrometer to 250 micrometers to a pretreatment temperature of 100° C. to 180° C. to form a pretreated polyvinylidene chloride copolymer film and then heating and restraining the pretreated polyvinylidene chloride copolymer film to a maximum pyrolysis temperature from 350° C. to 750° C.

A power production system includes a flue gas generator configured to generate a flue gas that includes carbon dioxide and oxygen; a fuel supply; a fuel cell assembly that includes: a cathode section configured to receive the flue gas generated by the flue gas generator, and output cathode exhaust, and an anode section configured to receive fuel from the fuel supply, and output anode exhaust that contains hydrogen and carbon dioxide; a methanator configured to receive the anode exhaust, convert at least a portion of the hydrogen in the anode exhaust to methane, and output methanated anode exhaust; a chiller assembly configured to cool the methanated anode exhaust to a predetermined temperature so as to liquefy carbon dioxide in the methanated anode exhaust; and a gas separation assembly configured to receive the cooled methanated anode exhaust and separate the liquefied carbon dioxide from residual fuel gas.

The invention is an improved method of making a carbon molecular sieve (CMS) membrane in which a polyimide precursor polymer is pyrolyzed to form a carbon molecular sieve membrane by heating, in a furnace, said polyimide precursor polymer to a final pyrolysis temperature of 600 C to 700 C at a pyrolysis heating rate of 3 to 7 C/minute from 400 C to the final pyrolysis temperature, the final pyrolysis temperature being held for a pyrolysis time of at most 60 minutes in a non-oxidizing atmosphere. In a particular embodiment, the cooling rate from the pyrolysis temperature is accelerated by methods to remove heat. The CMS membranes have shown an improved combination of selectivity and permeance as well as being particularly suitable to separate gases in gas streams such methane from natural gas, oxygen from air and ethylene or propylene from light hydrocarbon streams.

The invention relates to a system for separating and storing molecules, atoms and/or ions from air, wherein at least one air collecting means comprises at least one collecting tank configured to receive molecules, atoms and/or ions separated from air through an inlet and at least one membrane adapted to fit in the inlet of the collecting tank and configured to let a specified pre-determined size of molecules, atoms and/or ions to pass through the at least one membrane. The system further comprises at least one storing tank for storing the separated molecules, atoms and/or ions, and at least one outlet. The system according to the invention can be used to utilize the energy present in such molecules or separate unwanted gases present in the air.

The present disclosure relates to systems and methods useful for providing one or more chemical compounds in a substantially pure form. In particular, the systems and methods can be configured for separation of carbon dioxide from a process stream, such as a process stream in a hydrogen production system. As such, the present disclosure can provide systems and method for production of hydrogen and/or carbon dioxide.

An absorption liquid regeneration apparatus includes: a regeneration tower for regenerating a CO.sub.2 absorption liquid; a reflux water drum configured to separate released gas from the regeneration tower into CO.sub.2 gas and condensed water, and return the condensed water to the regeneration tower; and a cleaning part installed in a gas-phase part of the reflux water drum or in a CO.sub.2 flow passage through which the CO.sub.2 gas having flowed from the gas-phase part flows, and configured to remove a CO.sub.2 absorption agent contained in the CO.sub.2 gas by using a cleaning liquid. The cleaning liquid has a lower concentration of the CO.sub.2 absorption agent than the condensed water stored in a liquid-phase part of the reflux water drum.

An electrochemical reaction device comprises: an anode unit to oxidize water and thus generate oxygen; a cathode unit to reduce carbon dioxide and thus generate a carbon compound and hydrogen; a separator separating the anode and cathode units; and a power supply connected to the anode and cathode units, the cathode unit including: a porous member having a first surface and a second surface; a flow path plate facing the first surface; and a reduction catalyst on the second surface, and the flow path plate including: a flow path through which a target gas containing the carbon dioxide flows; and a porous film separating a first space and a second space inside the flow path and being permeated with an ionic liquid, the ionic liquid being configured to separate the carbon dioxide from the target gas.