Disclosed are metal organic frameworks (MOFs) for adsorbing guest species, methods for the separation of gases using the MOFs, and systems comprising the MOFs. The MOFs comprise a plurality of secondary building units (SBUs), each SBU comprising a repeating unit of one metal cation connected to another metal cation via a first moiety of an organic linker; a layer of connected adjacent SBUs in which a second moiety of the linker in a first SBU is connected to a metal cation of an adjacent SBU, and wherein adjacent layers are connected to each other via linker-to-linker bonding interactions

Process for catalytic oxidative removal of at least one oxidisable gaseous compound from a gas mixture comprising the at least one oxidisable gaseous compound as well as oxygen through the use of an oxidation catalyst, whereby the gas mixture is not a combustion flue gas, characterised in that the oxidation catalyst was produced through the use of at least one exothermic-decomposing platinum precursor.

A filtering device is provided for filtering pollutants from a gas stream. The device includes a cartridge comprising an inner perforated passage, an outer perforated jacket, one or more non-perforated ends and a sorbent bed contained between the inner passage and the outer jacket; and a outer shell containing the cartridge and having a first port in fluid communication with the inner perforated passage and a second port in fluid communication with the outer perforated jacket. A flowpath of the gas stream into any one of the first port or the second port, through the sorbent bed and out of the other of the first port or the second port is a bidirectional flowpath. A method is further provided for filtering pollutants from a gas stream. The method includes the steps of allowing the gas stream to flow into a filtering device in a first direction, the device comprising a cartridge having a sorbent bed contained therein; directing the gas stream to bend in a second direction differing from the first direction as it enters the sorbent bed; and allowing the gas stream to pass through the sorbent bed and to exit the device.

A methane destruction apparatus for capturing and converting fugitive methane gas emissions into carbon dioxide and water comprises a methane-capturing module for capturing the fugitive methane gas emissions and a methane conversion module for receiving captured methane from the methane-capturing module. The methane-capturing module includes a fugitive methane gas emission intake connected to an emissions line having a backpressure equal to 1 to 3 inches of water (249 to 746 Pa), a natural gas feed for feeding natural gas into the methane-capturing module, may include a relief vent for preventing overpressure within the methane-capturing module and a drain for draining liquids that have condensed within the methane-capturing module. The methane conversion module includes a conversion pad for catalytically converting the captured methane into carbon dioxide and water, a water vapour opening for outputting the water and a carbon dioxide opening for outputting the carbon dioxide.

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 (GI), a second gas (G2) and a third gas (G3) becomes less than or equal to the 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 the third gas (G3) 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 of the second gas (G2).

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).

An interface seal assembly for sealing a tubular filter element relative to a first component and a second component of a fluid filtration system. The interface seal assembly comprises an body located between the first and second components, and having: an aperture extending through the body for communicating with an internal cavity of the filter element; a first mounting surface comprising a first seal groove; and a second mounting surface opposite the first mounting surface, comprising a second seal groove. One of the first and second seal grooves has a circular shape, and the other has a non-circular shape. A first seal is located in the first seal groove, for sealing the interface body relative to one of the first and second components. A second seal is located in the second seal groove, for sealing the body relative to the other of the first and second components.

Entrained metal hydride particle are removed from a flow of hydrogen from a Mg-based hydride storage unit using not only a particle filter but improvements for reducing or eliminating drastic changes in flow. In addition to or alternative to removal of entrained metal hydride particles, methane produced by reaction of hydrogen with steel in a metal hydride system preferably operated above 350° C. is removed downstream of the Mg-based hydride storage unit using an adsorption cartridge, preferably containing activated carbon.

A method of selectively catalytically oxidizing dinitrogen oxide present in a gaseous sample, comprising: heating a NiO catalyst to a temperature of at least 250° C.; and bringing the gaseous sample into contact with the heated NiO catalyst to oxidize dinitrogen oxide of the gaseous sample in the presence of the heated NiO catalyst.

A process and apparatus for producing a hydrogen-enriched product and recovering CO.sub.2 from an effluent stream from a hydrogen production process unit are described. The process utilizes a CO.sub.2 recovery system integrated with a PSA system that produces at least two product streams to recover additional hydrogen and CO.sub.2 from the tail gas stream of a hydrogen PSA unit in the hydrogen production process.