A neon recovering/purifying system including: a recovery vessel that is arranged on an exhaust gas route and stores exhaust gas, the exhaust gas route being branched and extending from a discharge line; a compressor that increases a pressure of the exhaust gas sent out from the recovery vessel, to a third pressure; an exhaust gas flow rate regulating unit that regulates a flow rate of the exhaust gas whose pressure has been increased by the compressor; a first impurity removing unit that removes a first impurity from the exhaust gas; a second impurity removing unit that removes a second impurity from the exhaust gas from which the first impurity has been removed; a pressure increasing vessel that stores purified gas that has been processed by the first impurity removing unit and the second impurity removing unit; a pressure reducing valve that reduces a pressure of the purified gas sent out from the pressure increasing vessel, to the first pressure; and a purified gas flow rate regulating unit that regulates a flow rate of the purified gas supplied to a supply line of a manufacturing system.

The present invention relates to a process for processing a gas mixture comprising methane, carbon dioxide, carbon monoxide, hydrogen, nitrogen, argon and traces of olefins and oxygenates. Methane, carbon dioxide and carbon monoxide, and optionally hydrogen, can be recovered from the gas mixture in a very efficient way.

The present invention provides a composite body having, on a porous substrate and in the interstices of the substrate that includes fibers, preferably of an electrically nonconductive material, a porous layer (1) composed of oxide particles bonded to one another and partly to the substrate that include at least one oxide selected from oxides of the elements Al, Zr, Ti and Si, preferably selected from Al.sub.2O.sub.3, ZrO.sub.2, TiO.sub.2 and SiO.sub.2, and having, at least on one side, a further porous layer (2) including oxide particles bonded to one another and partly to layer (1) that include at least one oxide selected from oxides of the elements Al, Zr, Ti and Si, preferably selected from Al.sub.2O.sub.3, ZrO.sub.2, TiO.sub.2 and SiO.sub.2, where the oxide particles present in layer (1) have a greater median particle size than the oxide particles present in layer (2), which is characterized in that the median particle size (d.sub.50) of the oxide particles in layer (1) is from 0.5 to 4 m and the median particle size (d.sub.50) of the oxide particles in layer (2) is from 0.015 to 0.15 m, preferably 0.04 to 0.06 m, a process for producing corresponding composite bodies and for the use thereof, especially in gas separation.

A host material may be used for the separation of elements or compounds, wherein the host material is an organic molecular solid with suitable cavities for accommodating a guest material to be separated, and with interconnections between the cavities to allow the guest material to diffuse through the host material, and wherein said interconnections are closed for a proportion of the time or have a static pore limiting diameter which is smaller than the static dimension of the guest material. Applications include separations of rare gases, chiral molecules, and alkanes. One class of suitable host materials may be made by imine condensation.

The gas separation method is executed under a condition in which a partial pressure of a first gas (G1) in a feed gas that contains at least mutually different gases being the first gas (G1) and a second gas (G2) becomes less than or equal to a total pressure of a permeate-side space (S2) of a gas separation membrane (30). The gas separation method includes a step of causing flow of a sweep gas that contains at least a third gas (G3) being a different gas from the first gas (G1) and the second gas (G2) into the permeate-side space (S2) of the gas separation membrane (30) while supplying a feed gas to a feed-side space (S1) of the gas separation membrane (30). The permeation rate of the first gas (G1) in the gas separation membrane (30) is greater than the permeation rate respectively of the second gas (G2) and the third gas (G3).

A gas separation membrane for selective separation of hydrogen and helium from gas mixtures containing carbon dioxide includes a porous support layer, an aromatic polyamide layer on the porous support layer, and a coating including a glassy polymer formed on the aromatic polyamide layer. A glass transition temperature of the glassy polymer is greater than 50 C. The gas separation membrane may be formed by contacting a solution including the glassy polymer with an aromatic polyamide layer of a composite membrane and drying the solution to form a coating of the glassy polymer on the aromatic polyamide layer. Separating hydrogen or helium from a gas stream including carbon dioxide includes contacting a gas feed stream including carbon dioxide with the gas separation membrane to yield a permeate stream having a concentration of helium or hydrogen that exceeds the concentration of helium or hydrogen, respectively, in the gas feed stream.

Disclosed herein is a gas separation membrane comprising a furan-based polymer, an apparatus comprising the gas separation membrane, and a process for separating a mixture of gases using said gas separation membrane. The process comprises contacting one side of a gas separation membrane comprising a furan-based polymer with a mixture of gases having different gas permeances, whereby at least one gas from the mixture of gases permeates preferentially across the gas separation membrane, thereby separating the at least one gas from the mixture of gases.

The present invention discloses high selectivity copolyimide membranes for gas, vapor, and liquid separations. Gas permeation tests on these copolyimide membranes demonstrated that they not only showed high selectivity for CO.sub.2/CH.sub.4 separation, but also showed extremely high selectivities for H.sub.2/CH.sub.4 and He/CH.sub.4 separations. These copolyimide membranes can be used for a wide range of gas, vapor, and liquid separations such as separations of CO.sub.2/CH.sub.4, He/CH.sub.4, CO.sub.2/N.sub.2, olefin/paraffin separations (e.g. propylene/propane separation), H.sub.2/CH.sub.4, He/CH.sub.4, O.sub.2/N.sub.2, iso/normal paraffins, polar molecules such as H.sub.2O, H.sub.2S, and NH.sub.3 mixtures with CH.sub.4, N.sub.2, H.sub.2. The high selectivity copolyimide membranes have UV cross-linkable sulfonyl functional groups and can be used for the preparation of UV cross-linked high selectivity copolyimide membranes with enhanced selectivities. The invention also includes blend polymer membranes comprising the high selectivity copolyimide and polyethersulfone. The blend polymer membranes comprising the high selectivity copolyimide and polyethersulfone can be further UV cross-linked under UV radiation.

A system for providing hydrogen includes a first electrochemical cell or stack including a first cathode and a first anode separated by a first proton exchange membrane. A first inlet is in communication with the anode side of the first electrochemical cell or stack. The first inlet receives a first gas including hydrogen. A liquid composition on a liquid flow path is in communication with the cathode side of the first electrochemical cell or stack. The liquid composition includes water and a water-compatible redox compound. A second electrochemical cell stack including a second cathode and a second anode separated by a second proton exchange membrane is disposed with the anode side of the second electrochemical cell or stack in communication with the liquid flow path. A hydrogen outlet in communication with the cathode side of the second electrochemical cell or stack dispenses hydrogen from the system.

Some embodiments of the disclosure correspond to, for example, a method for controlling a scrubber containing an adsorbent. The scrubber may be configured to cycle between scrubbing at least one pollutant/gas from a stream of gases with the pollutant/gas being adsorbed onto the adsorbent, and regenerating at least some of the adsorbent and thereby purging at least some of the one pollutant and/or first gas from the adsorbent via a regeneration gas flow. The method may include flowing a stream of gases through the scrubber, the scrubber including the adsorbent and adsorbing at least some of the one pollutant/gas from the stream of gases onto the adsorbent during an adsorption phase over a first time period. The method may also include purging at least a portion of the one pollutant/gas from the adsorbent during a regeneration phase over a second time period with a regeneration gas flow, and cycling therebetween.