In a broad form the present invention relates to a method for oxidation of a species comprising sulfur in an oxidation state below +4, such as H.sub.2S, CS.sub.2, COS and S.sub.8 vapor, to SO.sub.2 said method comprising the step of contacting the gas and an oxidant with a catalytically active material consisting of one or more elements taken from the group consisting of V, W, Ce, Mo, Fe, Ca, Mg, Si, Ti and Al in elemental, oxide, carbide or sulfide form, optionally with the presence of other elements in a concentration below 1 wt %, at a temperature between 180° C. and 290° C., 330° C., 360° C. or 450° C., with the associated benefit of such a temperature being highly energy effective, and the benefit of said elements having a low tendency to form sulfates under the conditions, with the related benefit of an increased stability of the catalytically active material. The other elements present may be catalytically active noble metals or impurities in the listed materials.

The invention relates to a process for removing a target gas from a gas stream rich in the target gas and to an absorbent solution for absorbing a gas, such as carbon dioxide, from a gas stream. The invention involves the use of a photoactive compound that is convertible from a first state to a second state upon irradiation to facilitate removal or collection of a target gas from a gas stream.

Disclosed herein are asymmetric multilayer carbon molecular sieve (“CMS”) hollow fiber membranes and processes for preparing the membranes. The processes include simultaneously extruding a core dope containing a polymer and suitable nanoparticles, a sheath dope, and a bore fluid, followed by pyrolysis of the extruded fiber.

The process for configuring or reconfiguring a sulfur removal plant having a plurality of Claus units that is greater than the number of downstream tail gas treating units (TGTUs) is disclosed. The process allows for the regeneration of one of the Claus units without shutting down any of the downstream TGTUs or the other Claus units. Specifically, the regeneration tail gas can be diverted to the reaction furnace of an in-service Claus unit, thereby allowing excess oxygen to be used to regenerate the Claus unit more efficiently, and without exceeding environmental SO.sub.2 emission requirements.

This disclosure relates to a process for removing acid gases from a gas stream enriched in acid gases, wherein: (a) the gas stream enriched in acid gases is contacted in an absorption zone with an absorption medium, wherein the absorption medium is an aqueous medium comprising an amine, to form a gas stream depleted in acid gases which comprises an entrained amine and an absorption medium enriched in acid gases; and (b) treating the gas stream depleted in acid gases which comprises an entrained amine in a scrubbing zone with a scrubbing medium, wherein the scrubbing medium is an aqueous medium comprising an amine, the amount of amine comprised by the scrubbing medium being about 0 to about 10.0 wt. %, to form a gas stream depleted in acid gases and in amine and a scrubbing medium enriched in amine.

Embodiments provide a method of compound removal from a fluid. The method includes contacting one or more metal organic framework (MOF) compositions with a fluid and sorbing one or more compounds, such as CO.sub.2, H.sub.2S and condensable hydrocarbons. One or more of CO.sub.2, H.sub.2S and condensable hydrocarbons can be sorbed simultaneously or in series. The metal organic framework can be an M-soc-MOF.

The invention relates to a method for preparing a solid comprising the mixture of a set of compounds comprising at least one Cu.sub.2(OH).sub.2CO.sub.3 powder, one metal oxide powder selected from the group of metals consisting of copper, zinc, iron, manganese and mixtures thereof, and at least one binder as well as the use of the solid prepared by means of this method.

The present invention relates to an aqueous alkanolamine solution demonstrating low volatility comprising 2-di-methylamino-2-hydroxymethyl-1, 3-propanediol useful for removing acid gases from gaseous mixtures. Said aqueous alkanolamine solution may further comprise one or more of an acid or acid-forming compound, another amino compound, an activator, a physical solvent, or one or more other compounds used in gal-liquid treatment practices. Further, the present invention relates to a process for removing acid gases from a gaseous mixture, preferably hydrogen sulfide, comprising the step of contacting the gaseous mixture with said aqueous alkanolamine solution. Examples of the gaseous mixtures include natural gas, synthesis gas, tail gas, and refinery gas.

A method of removing impurities from a natural gas stream. A selective solvent is provided that absorbs a first impurity at a first rate and a second impurity at a second rate that is slower than the first rate. The solvent is cooled to a temperature below 60° F. to provide a cooled solvent. The cooled solvent is contacted with the natural gas stream, thereby generating a rich solvent that includes the first impurity. The rich solvent is removed from the natural gas stream, wherein an amount of the first impurity remaining in the natural gas stream is below a sales gas requirement.

A process for the oxidation of hydrogen sulfide to sulfur trioxide with subsequent sulfur trioxide removal comprises oxidizing hydrogen sulfide to sulfur trioxide in at least one catalyst-containing reactor and feeding the effluent from the last reactor to a candle filter unit for SO.sub.3 removal, where it is mixed with an injected alkaline sorbent slurry or powder to form an alkali sulfate and a hot clean gas. Preferably the oxidation is done in two reactors, the first oxidizing H.sub.2S to SO.sub.2 over a monolith type catalyst and the second oxidizing SO.sub.2 to SO.sub.3 over a VK type catalyst.