A fuel oxidation system including an inlet in fluid communication with an interior of a sealed container, and the sealed container is holding permeated gas released from a pressure vessel within the sealed container. Another inlet is in fluid communication with an environment surrounding the sealed container, and the environment includes oxygen gas (O.sub.2). An oxidation module is in fluid communication with the inlet and the other inlet, and the oxidation module is combining the permeated gas received by the inlet with the oxygen gas (O.sub.2) received by the other inlet to form a preferred substance.

A method for filtering gas includes providing a gas filtration structure, and the gas filtration structure includes a porous support and a first gas filtration film pair on the porous support, wherein the first gas filtration film pair includes a first hydrogen permeation layer and a first calcinated layered double hydroxide (c-LDH) layer, and the first hydrogen permeation layer is disposed between the porous support and the first c-LDH layer. The method also provides a hydrogen-containing mixture gas over the first gas filtration film pair, and collects hydrogen under the porous support.

A microporous polymeric composition including a matrix polymer having a fractional free volume of at least 0.1 and dispersed particles having a hypercrosslinked polymer.

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 hydrogen gas recovery system according to the present ingestion is configured by a condensation and separation apparatus (A) that condenses and separates chlorosilanes from a hydrogen-containing reaction exhaust gas exhausted from a polycrystalline silicon production step, a compression apparatus (B) that compresses the hydrogen-containing reaction exhaust gas, an absorption apparatus (C) that absorbs and separates hydrogen chloride by contacting the hydrogen-containing reaction exhaust gas with an absorption liquid, a first adsorption apparatus (D) comprising an adsorption column filled with activated carbon for adsorbing and removing methane, hydrogen chloride, and part of the chlorosilanes each contained in the hydrogen-containing reaction exhaust gas, a second adsorption apparatus (E) comprising an adsorption column filled with synthetic zeolite that adsorbs and removes methane contained in the hydrogen-containing reaction exhaust gas, and a gas line (F) that recovers a purified hydrogen gas having a reduced concentration of methane.

A process is provided for increasing the recovery of high-purity hydrogen from a steam cracking process in situations where byproduct methane yield is high relative to hydrogen. After a hydrocarbon gas stream is sent through a cold box and demethanizer, a small proportion of methane is sent through a pressure swing adsorption unit separately from a gas stream that contains hydrogen to increase high-purity hydrogen recovery by about 6%.

A vanadium alloy essentially consisting of: vanadium; and aluminium having a content of greater than 0 to 10 at %, and a process of producing thereof.

Electrochemical cells (e.g., fuel cells or electrochemical gas extraction cells) supplied with power-to-gas mixtures of dilute hydrogen concentrations may be remarkably improved by the use of porous gas layer electrodes. The electrochemical cells may comprise a first porous gas layer gas diffusion electrode, a second porous gas layer gas diffusion electrode, and a liquid electrolyte Sin contact with the first and second electrodes. The porous gas layers may each comprise a porous, non-conductive, liquid-impermeable material that dramatically improves cell performance.

A process is disclosed for producing hydrogen for a hydrogen consuming process comprising obtaining a gas stream containing hydrogen from a steam reforming hydrogen plant, sending the gas stream to a pressure swing adsorption unit to be separated into a hydrogen stream and a fuel gas stream; purging the pressure swing adsorption unit with an external purge gas stream from a hydroprocessing unit off gas; treating the off gas with a thermal swing adsorption unit to remove water and other impurities prior to purging the pressure swing adsorption unit; and using a protective adsorbent layer in the pressure swing adsorption unit at the product-hydrogen end of the bed to adsorb impurities from the external purge gas.

The present invention provides a gas separation system and a gas separation method capable of separating various types of hydrocarbon gas with high selectivity, and a gas separation system is for separating one type or more of hydrocarbon gases from mixed gas consisting of two types or more of hydrocarbon gases; having a porous metal-organic complex having pores determined by metal ion-containing planar ligands facing each other and pillar ligands coordinating between the planar ligands, and a controller for controlling at least a pressure of the mixed gas; and in which the pressure is controlled to control adsorption of the hydrocarbon gas to the porous metal-organic complex or desorption thereof from the porous metal-organic complex.