Copper sulfide of the formula Cu.sub.xS.sub.y, wherein x and y are integer or non-integer values, wherein (i) the copper sulfide has a sulfur 2p XPS spectrum with peaks at 162.3 eV (±1 ev), 163.8 eV (±1 ev) and 68.5 eV (±1 ev), characterised in that the peak at 168.5 eV has a lower value of counts per second (CPS) than both the peak at 162.3 eV and the peak at 163.8 eV; and (ii) the copper sulfide has a copper 2p XPS spectrum with peaks at 932.0 eV (±2 ev) and 933.6 eV (±3 eV) and characterised in that the XPS spectrum does not comprise identifiable satellite peaks at 939.8 eV and 943.1 eV (±3 eV).

Primary, secondary (1°,2°) alkylethylenediamine- and alkylpropylenediamine-appended variants of metal-organic framework are provided for CO.sub.2 capture applications. Increasing the size of the alkyl group on the secondary amine enhances the stability to diamine volatilization from the metal sites. Two-step adsorption/desorption profiles are overcome by minimzing steric interactions between adjacent ammonium carbamate chains. For instance, the isoreticularly expanded framework Mg.sub.2(dotpdc) (dotpdc.sup.4−=4,4″-dioxido-[1,1′:4′,1″-terphenyl]-3,3″-dicarboxylate), yields diamine-appended adsorbents displaying a single CO.sub.2 adsorption step. Further, use of the isomeric framework Mg-IRMOF-74-II or Mg.sub.2(pc-dobpdc) (pc-dobpdc.sup.4−=3,3-dioxidobiphenyl-4,4-dicarboxylate, pc=para-carboxylate) also leads to a single CO.sub.2 adsorption step with bulky diamines. By relieving steric interactions between adjacent ammonium carbamate chains, these frameworks enable step-shaped CO.sub.2 adsorption, decreased water co-adsorption, and increased stability to diamine loss. Variants of Mg.sub.2(dotpdc) and Mg.sub.2(pc-dobpdc) functionalized with large diamines such as N-(n-heptyl)ethylenediamine have utility as adsorbents for carbon capture applications.

A hydrocarbon-forming gas compression method comprising: a hydrate formation step in which water and hydrate-forming gas are mixed at a first pressure and a first temperature, resulting in the formation of hydrate; a decomposition step in which the hydrate is warmed, and the hydrate is decomposed to re-generate hydrate-forming gas at a second pressure higher than the first pressure.

A system and method for removing hydrogen sulfide from natural gas using a triazine scavenger is described. The system includes a pre-treatment system that can be connected to an existing hydrogen sulfide removal system to more fully utilize the triazine scavenger. The pre-treatment system includes a contactor vessel in which sour natural gas is contacted with fresh and/or partially consumed scavenger to partially sweeten the sour gas by removing H.sub.2S. The partially sweetened gas then flows to the existing hydrogen sulfide removal system where it is fully sweetened.

Embodiments of the present disclose provide a method of sorbing one or more compounds from a fluid, wherein the method may include contacting a M-soc-MOF composition with a fluid containing at least H.sub.2S and one or more of CO.sub.2 and CH.sub.4; and sorbing at least H.sub.2S from the fluid. Embodiments of the present disclosure provide a membrane that may include a metal-organic framework (MOF) composition, wherein the MOF composition includes a M-soc-MOF composition, where M is a metal and soc is a square-octahedral topology, and wherein the M-soc-MOF composition is a continuous thin film on a support.

The invention relates to a process (100) for producing liquefied natural gas using a feedstock mixture that contains at least methane, one or more components boiling at a temperature lower than methane and one or more hydrocarbons boiling at a temperature higher than methane, wherein the hydrocarbon(s) boiling at a temperature higher than methane comprise one or more hydrocarbons freezing at a higher temperature, with a freezing point higher than −50° C. According to the invention the feedstock mixture is fed into a pressure swing adsorption process (10), in which a first fraction containing methane and a second fraction containing methane are formed, the first fraction containing methane contains, in addition to the methane, at least the predominant portion of the components of the feedstock mixture that boil more readily than methane and is low in or free from the hydrocarbons boiling less readily than methane, and the second fraction containing methane contains, in addition to the methane, at least the predominant portion of the hydrocarbons from the feedstock that boil less readily than methane and is low in or free from the components that boil more readily than methane, and the first fraction containing methane, or a portion thereof, is supplied for liquefaction (20). The invention also relates to a corresponding plant.

This invention provides a composition comprising I. at least one reaction product between a nitrogen-free monohydric alcohol and an aldehyde or ketone, and II. at least one reaction product between a monosaccharide having 3 to 6 carbon atoms and/or an oligosaccharide being formed by oligomerization of monosaccharides having 3 to 6 carbon atoms and an aldehyde or ketone, and optionally III. at least one reaction product from III.a) formaldehyde, and III.b) an amine, selected from the group consisting of primary alkyl amines having 1 to 4 carbon atoms, and primary hydroxy alkyl amines having 2 to 4 carbon atoms, and optionally IV. at least one solid suppression agent selected from the group consisting of IV(a). alkali or alkaline earth metal hydroxides IV(b). mono-, di- or tri-hydroxy alkyl, aryl or alkylaryl amines, IV(c). mono-, di- or tri-alkyl, aryl or alkylaryl primary, secondary and tertiary amines or IV(d). multifunctional amines and IV(e). mixtures of compounds of groups IV(a) to IV(c). wherein alkyl is C.sub.1 to C.sub.15, aryl is C.sub.6 to C.sub.15 and alkylaryl is C.sub.7 to C.sub.15.

A method for carbon dioxide recycle stream processing with ethylene glycol dehydrating in an enhanced oil recovery process includes receiving a first carbon dioxide recycle stream from a hydrocarbon formation, adding ethylene glycol to the first carbon dioxide recycle stream to produce an ethylene glycol and carbon dioxide recycle stream, condensing the ethylene glycol and carbon dioxide stream to produce a multiphase stream, separating the multiphase stream into a water and ethylene glycol stream and a second carbon dioxide recycle stream, separating the water and ethylene glycol stream into a water stream and an ethylene glycol stream, and separating the second carbon dioxide recycle steam into a carbon dioxide reinjection stream and a natural gas liquids stream.

An apparatus and method for flow management and CO.sub.2-recovery from a CO.sub.2 containing hydrocarbon flow stream, such as a post CO.sub.2-stimulation flowback stream. The apparatus including a flow control zone, a gas separation zone, a pretreatment zone, and a CO.sub.2-capture zone. The CO.sub.2-capture zone is in fluid communication with the pretreatment zone to provide CO.sub.2-capture from a pretreated flowback gas stream and output a captured CO.sub.2-flow stream. The CO.sub.2-capture zone includes a first CO.sub.2-enricher and at least one additional CO.sub.2 enricher disposed downstream of the first CO.sub.2 enricher and in cascading relationship to provide a CO.sub.2-rich permeate stream, the CO.sub.2-capture zone further including at least one condenser to condense the enriched CO.sub.2-stream and output the captured CO.sub.2-flow stream.

A high selectivity and high CO.sub.2 plasticization resistant polymer comprises a plurality of repeating units of formula (I) for gas separation applications. The polymer may be synthesized from a superacid catalyzed poly(hydroalkylation) reaction.

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Membranes made from the polymer and gas separation processes using the membranes made from the polymer are also described.