A hybrid method for capturing CO.sub.2 from a gas mixture is provided, comprising a step of contacting the CO.sub.2 containing gas mixture with a slurry consisting of a liquid medium, imidazole or imidazole derivative(s), and a metal-organic framework material (MOFs). For the slurry system, the mass fraction of the imidazole or imidazole derivative(s) in it ranging from 2 to 50% and the mass fraction of the metal-organic framework material in it ranging from 5 to 25%. In the technical solution provided in the present invention, through combining absorptive separation by the liquid solution in which the imidazole or imidazole derivative(s) is dissolved, adsorption separation by the MOF material suspended in the solution, and selective permeation separation by a liquid medium film forms on the outside surface of the suspended MOFs, an absorption-adsorption hybrid separation effect for CO.sub.2 gas mixtures is efficiently achieved. In the CO.sub.2 capture method provided in the present invention, conventional absorption separation and adsorptive separation technologies are effectively combined, furthermore, the addition of imidazole or imidazole derivative(s) substantially increases both the CO.sub.2 capture ability and capture amount of the MOFs/liquid slurry, showing a great potential in industrial applications.

The absorption agent of the present invention contains water, an amine compound, and an organic solvent, and a value obtained by subtracting a solubility parameter of the organic solvent from a solubility parameter of the amine compound is 1.1 (cal/cm.sup.3).sup.1/2 or more and 4.2 (cal/cm.sup.3).sup.1/2 or less. The method for separation and recovery of an acidic compound of the present invention includes the steps of: bringing a mixed gas containing an acidic compound into contact with an absorption agent containing water, an amine compound, and an organic solvent to absorb the acidic compound into the absorption agent; causing the absorption agent that has absorbed the acidic compound to be phase-separated into a first phase containing the acidic compound in a high content and a second phase containing the acidic compound in a low content; and heating the first phase to release the acidic compound from the first phase

Solvent absorption processes for separating components of an impure feed gas are disclosed. The processes involve two stages of gas purification. The acid gases including hydrogen sulfide, carbon dioxide and other sulfur compounds are simultaneously removed from the feed gas by contact with a physical solvent in two stages. The subject matter disclosed provides improved processes to reduce the operating costs of the system.

This invention is directed to methods and systems for controlling water in acid gas removal processes comprising the steps of a) treating the gas stream in an absorption zone with the NAS absorption liquid; b) direction the acid gas-loaded NAS absorption liquid to a regeneration zone; c) directing the regenerated NAS absorption liquid to step a); and d) controlling the first and second set of conditions.

A method for cleaning a contaminated solvent used to treat a gas stream, for example a contaminated glycol or a contaminated amine stream, by vacuum evaporation using a mechanically-maintained horizontally-orientated thin film evaporator, where the contaminant material is recovered from the thin film in solvent-free form, as either a heavy organic material or as free flowing salts.

A plant comprises a feed gas source, H2S removal unit, first absorber and a second, pressure reduction stages, first and second heat exchangers, stripping unit, and a conduit. The H2S removal unit selectively removes H2S from a feed gas from the feed gas source to produce an H2S depleted feed gas. The first absorber and the second absorber remove CO2 from the H2S depleted feed gas using a semi-lean and an ultralean solvent to produce a product gas and a rich solvent. The plurality of pressure reduction stages generates a cooled flashed solvent. The first heat exchanger and the second heat exchanger use the cooled flashed solvent to cool the H2S depleted feed gas and the semi-lean solvent. The stripping unit strips the flashed solvent with dried air to produce the ultralean solvent, and the conduit combines a portion of the ultralean solvent with the H2S depleted feed gas.

Processes and apparatuses for treating a sour synthesis gas are provided. The process comprises passing the sour synthesis gas stream to an acid gas removal unit to provide a treated synthesis gas stream and a CO.sub.2 rich stream. At least a portion of the CO.sub.2 rich stream is passed to a thermal oxidizer unit to provide a treated CO.sub.2 gas stream. At least a portion of the treated synthesis gas stream is passed to a pressure swing adsorption unit to obtain a purified hydrogen stream and a tail gas stream. At least a portion of the tail gas stream is passed to the thermal oxidizer unit.

A desulfurization and denitration agent which is a mixture of polyalcohol and/or polyglycol substances, polycarboxylic acid substances and alkaline substances heated to above 90 C. and yielding, after condensation and/or polymerization, macromolecular or high-polymer ethers and/or esters for use in removing sulfur dioxides and/or nitrogen oxides from gases.

An absorbent for selective removal of hydrogen sulfide from a fluid stream comprising carbon dioxide and hydrogen sulfide comprises a) an amine compound of the formula (I)

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in which X, R.sup.1 to R.sup.7, x, y and z are as defined in the description; and b) a nonaqueous solvent; where the absorbent comprises less than 20% by weight of water. Also described is a process for selectively removing hydrogen sulfide from a fluid stream comprising carbon dioxide and hydrogen sulfide, wherein the fluid stream is contacted with the absorbent. The absorbent features high load capacity, high cyclic capacity, good regeneration capacity and low viscosity.

The present invention relates to a carbon dioxide absorbent comprising a triamine, a diamine and a dialkylene glycol dialkyl ether or trialkylene glycol dialkyl ether. The carbon dioxide absorbent according to the present invention can improve the carbon dioxide absorption capacity, absorption rate, and regeneration performance thereof simultaneously by using the triamine as a main absorbent, the diamine as a rate enhancer, the dialkylene glycol dialkyl ether or trialkylene glycol dialkyl ether as a fine disproportionation agent and a regeneration promoter.