An on-board fuel separation system includes a supply fuel tank configured to store an input fuel stream; a fuel separator fluidly coupled to the supply fuel tank and configured to separate the input fuel stream into a first fractional fuel stream and a second fractional fuel stream. The fuel separator includes a membrane that includes a plurality of pores sized based on a molecular size of one or more components of the first fractional fuel stream. The system includes a first fractional fuel tank fluidly coupled to the fuel separator to receive the first fractional fuel stream passed through the membrane and defined by a first auto-ignition characteristic value. The system includes a second fractional fuel stream coupled to the fuel separator to receive the second fractional fuel stream from the fuel separator that is defined by a second auto-ignition characteristic value that is different than the first auto-ignition characteristic value.

Provided are a methane-selective composite membrane comprising: a UiO-66 type organic-inorganic composite nanoporous material, a MIL-100 type organic-inorganic composite nanoporous material, or a ZIF-8 type organic-inorganic composite nanoporous material to which a methane-selective functional group is introduced for selectively separating methane from a gas mixture containing methane/nitrogen, a use thereof, and a method of preparing the same.

Perforated graphene sheets can be used in forming separation membranes. Separation membranes of the present disclosure, which can be used in gas separation processes in some embodiments, can include one or more polymer layers and one or more layers of perforated graphene. Methods for separating a gas mixture can include contacting a gas mixture with the separation membranes, and transiting one or more of the gases through the perforated graphene so as to affect separation.

A membrane system includes a first membrane and a second membrane. At a given temperature and pressure: the first membrane has a permeation rate for a first gas and a selectivity for a gas mixture comprising the first gas a second gas different from the first gas; the second membrane has a permeation rate for the first gas and a selectivity for the gas mixture; the permeation rate of the first membrane is greater than the permeation rate of the second membrane; and the selectivity of the second membrane is greater than the selectivity of the first membrane.

A system including biogas purification and provides biogas as feedstock to a solid oxide fuel cell. The biogas purification treatment process provides a polished biogas that is substantially free of carbonyl sulfides and hydrogen sulfide. The system uses a biogas treatment apparatus, that includes apparatus such as a packed columns, comprising copper oxide or potassium permanganate packing material, and an activated carbon component configured to treat the biogas by polishing it to remove carbonyl sulfides and deleterious trace residues, such as hydrogen sulfide, that were not removed by any prior bulk H2S removal steps. In addition, an oil removal device is used to remove any entrained fine oil droplets in the biogas. A polished biogas having in the range of 60% methane is charged to the fuel cell. Electricity generated may be fed into a grid or used directly as energy to charge electrical-powered vehicles, for example. Energy credits are tracked in real time and are appropriately assigned.

Refining assemblies and methods for refining rich natural gas containing a first methane gas and other hydrocarbons that are heavier than methane gas are disclosed. In some embodiments, the assemblies may include a methane-producing assembly configured to receive at least one liquid-containing feed stream that includes water and rich natural gas and to produce an output stream therefrom by (a) converting at least a substantial portion of the other hydrocarbons of the rich natural gas with the water to a second methane gas, a lesser portion of the water, and other gases, and (b) allowing at least a substantial portion of the first methane gas from the rich natural gas to pass through the methane-producing assembly unconverted. The assemblies may additionally include a purification assembly configured to receive the output stream and to produce a methane-rich stream therefrom having a greater methane concentration than the output stream.

A method for removing hydrogen sulfide (H.sub.2S) from an acid gas comprises feeding the gas to a membrane separation unit, collecting the product gas from the membrane unit, heating the permeate stream to the necessary inlet temperature for catalytic oxidation of H.sub.2S and feeding the heated permeate stream to a catalytic oxidation unit, where H.sub.2S is oxidized to SO.sub.2. The heating of the permeate stream is accomplished by using a fraction of the feed gas to heat the permeate stream in a separate heater or by using a steam-fired heater. The method is especially suited for use on an off-shore facility.

A gas separation membrane has a gas separation layer containing a crosslinked cellulose resin. The crosslinked cellulose resin has a particular linking structure in a crosslinked structure. The gas separation layer contains an organic solvent in a particular amount.

A gas separation asymmetric membrane includes a porous layer having gas permeability; and a compact layer having gas separation capability which is formed on the porous layer in which the gas separation asymmetric membrane is formed using a polyimide compound which has a structural unit represented by Formula (I) and at least one structural unit selected from a structural unit represented by Formula (II) or a structural unit represented by Formula (III) and in which the viscosity, at 25° C., of a solution obtained by dissolving the polyimide compound in N-methylpyrrolidone at a concentration of 5% by mass is in a range of 2.2 to 22.0 mPa.Math.sec,

##STR00001##

in the formula, X.sup.1 represents a group having a structure represented by Formula (I-a) or (I-b).

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A method for production of renewable natural gas (RNG) from biogases containing volatile organic compounds (VOCs) combines temperature swing adsorption (TSA) for removal of VOCs, a form of pressure swing adsorption (PSA) for nitrogen separation, and membrane gas separation technology for carbon dioxide removal. TSA systems may improve removal of VOCs relative to PSA systems, may reduce RNG plant operating costs, and may simplify RNG plant operation. Methane recovery may be improved by using equilibrium PSA systems instead of dynamic PSA systems for methane separation.