This disclosure may relate generally to systems, methods and devices for Direct Air Capturing of CO2 or methane from atmospheric or underwater vented sources.

A supported carbon molecular sieve (CMS) membrane is made by contacting a film of a carbon forming polymer on a polymer textile to form a laminate. The laminate is then heated to a temperature for a time under an atmosphere sufficient to carbonize the film and polymer textile to form the supported CMS membrane. The supported CMS membrane formed is a laminate having a carbon separating layer graphitically bonded to a carbon textile, wherein the carbon separating layer is a continuous film. The supported CMS membranes are particularly useful for separating gases such as olefins from their corresponding paraffins.

Hydrogen purification devices and their components are disclosed. In some embodiments, the devices may include at least one foil-microscreen assembly disposed between and secured to first and second end frames. The at least one foil-microscreen assembly may include at least one hydrogen-selective membrane and at least one microscreen structure including a non-porous planar sheet having a plurality of apertures forming a plurality of fluid passages. The planar sheet may include generally opposed planar surfaces configured to provide support to the permeate side. The plurality of fluid passages may extend between the opposed surfaces. The at least one hydrogen-selective membrane may be metallurgically bonded to the at least one microscreen structure. In some embodiments, the devices may include a permeate frame having at least one membrane support structure that spans at least a substantial portion of an open region and that is configured to support at least one foil-microscreen assembly.

The method of obtaining methane clathrates consists in the fact that pure methane or methane in a gas mixture not containing hydrocarbons other than methane in amounts not exceeding 1% is contacted with a mixture of alkanes from C7 to C16 and most preferably light paraffin oil containing alkanes from C10 to C14, at a temperature of 5 to 20° C. and absolute pressure above 1 bar, until the solvent is fully saturated.

An exhaust gas purification catalyst provides excellent removal performance of methane, which is chemically stable. Exhaust gas purification catalyst includes a substrate that divides cells through which an exhaust gas flows and a catalyst layer that is provided on a surface of the substrate. The catalyst layer includes a palladium layer containing palladium that extends from a first end part which is an end part on the side into which an exhaust gas in the cells flows to a second end part which is an end part on the side from which an exhaust gas flows out, a platinum layer containing platinum that extends from the second end part to the first end part, and a rhodium layer containing rhodium that is laminated with both the palladium layer and the platinum layer.

The present invention provides an exhaust gas purification catalyst having an excellent purification performance for purifying chemically stable methane. A catalyst material 30 includes a carrier 32 formed of alumina and a catalyst 34 formed of at least one of palladium and a palladium oxide directly supported on the carrier 32. A specific surface area of the carrier 32 is preferably 20 m.sup.2/g or more 90 m.sup.2/g or less. In one preferred aspect, a proportion of Pd(100) and PdO(101) in crystal planes of the catalyst 34 at a joint surface between the catalyst 34 and the carrier 32 is 20 number % or more.

When the product gas producing operation is stopped, a stand-by operation is executed in which a product gas filling up a reforming processing unit is circulated, in a state in which an adsorbent of adsorption towers is maintained in a state in which adsorption target components are desorbed, and the heating of a reformer by a heating burner is maintained, and when the stand-by operation is stopped and the product gas producing operation is started, initial operation processing is executed in which immediately after the start, a source gas and steam are supplied to the reformer to produce a reformed gas, and the reformed gas from the reforming processing unit supplied to the adsorption towers to produce the product gas, and then the product gas producing operation in which the product gas is collected in a product gas tank is executed.

A system that can eliminate engine combustion emissions in addition to raw and fugitive methane emissions associated with a gas compressor package. The system may comprise an air system for starting and instrumentation air supply; electrically operated engine pre/post-lube pump, compressor pre-lube pump, and cooler louver actuators; compressor distance piece and pressure packing recovery system; blow-down recovery system; engine crankcase vent recovery system; a methane leak detection system; and an overall remote monitoring system.

The present invention relates to a separation and recovery system and method of hydrogen from a coke oven gas (COG) in a steel industry, and more particularly, to a separation and recovery system and method of hydrogen from a coke oven gas (COG) in a steel industry, the system including a pre-processing unit removing impurities including tar, moisture, oil, hydrogen sulfide, and dusts from the coke oven gas (COG), a membrane separation unit including a polymer separation membrane module to generate a hydrogen concentrated gas stream by membrane-separating the coke oven gas (COG) processed in the pre-processing unit, and an adsorption unit separate and recover the hydrogen by allowing the hydrogen concentrated gas stream to contact an absorbent.

A hydrate formation promoter and the use thereof in methane storage. The hydrate formation promoter is a mixed aqueous solution including cyclopentane, sodium dodecyl sulfate and water, wherein a volume fraction of the cyclopentane is 5% to 23.4% and a mass fraction of the sodium dodecyl sulfate is 0.01% to 0.08%. The hydrate formation promoter can realize effective and rapid formation of methane hydrate at approximate room temperature (25° C.), and can remain stable at higher temperatures.