The combined acid gas removal and water filtration system (10) removes sour gases, such as hydrogen sulfide (H2S) and carbon dioxide (CO2), from an input gaseous hydrocarbon stream (FG), as well as producing purified water (TW). The acid gas removal system (10) has a contactor (12) for contacting the input gaseous stream (FG) with an absorption liquid solvent (ALS), and a stripper (24) for recycling the absorption liquid solvent (ALS) and removing acidic gases (AG) therefrom. A first heat exchanger (22) heats used absorption liquid solvent (UALS) output from the contactor (12) prior to injection into the stripper (24). A second heat exchanger (26) cools recycled absorption liquid solvent (RALS) using a refrigerant (R) before injection back into the contactor (12). The refrigerant (R) is coupled with an absorber (84), which receives a dilute ethanolic draw solution (DDS) from a forward osmosis filtration system (72), producing purified water (TW).

A method and a system for the removal of carbon dioxide from solvents.

Disclosed is a process for regenerating a hybrid solvent used to remove contaminants from a fluid stream and to provide an improved yield of purified fluid. Said process comprises at least one purification unit (12) and at least one regeneration unit (40) wherein condensed water (72) from the regeneration unit is combined with the regenerated lean hybrid solvent (55) prior to reuse in the purification unit and none of the condensed water is recycled into the regeneration unit.

The composite amine absorbing solution according to the present invention absorbs CO.sub.2 or H.sub.2S or both in a gas, and is obtained by dissolving a linear monoamine, a diamine, and an amide group-containing compound in water. By adopting this composite amine absorbing solution, the composites are interacting in a composite manner, due to an integrated effect of the components, the absorption property of CO.sub.2 or H.sub.2S or both is favorable, the desorption properties of the CO.sub.2 or H.sub.2S absorbed when regenerating the absorbing solution become favorable, and the amount of steam from a reboiler used when regenerating the absorbing solution in a CO.sub.2 recovery device can be reduced.

A sulfur dioxide absorbent that is an ionic liquid including a solvent; and a salt of a diamine compound that is substituted with a hydroxyl group and has a chemical formula 1 to 3 below dissolved in the solvent: ##STR00001## where, in Chemical Formula 1 and 2, R.sub.1-R.sub.4 are the same or different and each is independently selected from the group consisting of H, a C1-C6 alkyl, and a C1-C6 alkoxy; and where, in Chemical Formula 1 to 3, X is selected from the group consisting of Cl, Br, I, MeSO.sub.3, CF.sub.3SO.sub.3, HCO.sub.2, CF.sub.3CO.sub.2 and CH.sub.3CO.sub.2; and n is an integer of 1-10. The sulfur dioxide absorbent is constituted to selectively absorb sulfur dioxide and sulfurous acid (H.sub.2SO.sub.3) formed by combination of sulfur dioxide with water, not CO.sub.2.

A system and a process for capturing Carbon Dioxide (CO.sub.2) from flue gases are disclosed. The process comprises feeding a flue gas comprising CO.sub.2 to at least one Rotary Packed Bed (RPB) absorber rotating circularly. A solvent may be provided through an inner radius of the RPB absorber. The solvent may move towards an outer radius of the RPB absorber. The solvent may react with the flue gas in a counter-current flow. The process further includes passing the flue gas through at least one of a water wash and an acid wash to remove traces of the solvent present in the flue gas. Finally, the solvent reacted with the CO.sub.2 may be thermally regenerated for re-utilizing the solvent back in the process.

An absorbent liquid which absorbs at least one of CO.sub.2 and H.sub.2S from a gas, including a secondary linear monoamine; a tertiary linear monoamine or a sterically hindered primary monoamine; and a secondary cyclic diamine, wherein a concentration of each of the secondary linear monoamine, the tertiary linear monoamine or the sterically hindered primary monoamine; and the secondary cyclic diamine is less than 30% by weight.

A process for producing a deacidified fluid stream from a fluid stream comprising methanol and at least one acid gas, comprising a) an absorption step in which the fluid stream is contacted with an absorbent in an absorber to obtain an absorbent laden with methanol and acid gases and an least partly deacidified fluid stream; b) a regeneration step in which at least a portion of the laden absorbent obtained from step a) is regenerated in a regenerator to obtain an at least partly regenerated absorbent and a gaseous stream comprising methanol, water and at least one acid gas; c) a recycling step in which at least a substream of the regenerated absorbent from step b) is recycled into the absorption step a); d) a condensation step in which a condensate comprising methanol and water is condensed out of the gaseous stream from step b); e) a distillation step in which at least a portion of the condensate from step d) is guided into a distillation column to obtain a top stream comprising methanol and a bottom stream comprising water;

which comprises recycling at least a portion of the bottom stream from step e) into the regenerator.

An apparatus for deacidifying a fluid stream, comprising methanol and at least one acid gas, according to claim 1, comprising a) an absorber comprising an absorption zone, at least one feed for absorbent, a feed for the fluid stream to be deacidified, a liquid draw for the laden absorbent, a draw point for the deacidified fluid stream and optionally a rescrubbing zone with a feed for scrubbing agent; b) a regenerator comprising a regeneration zone, an evaporator, a feed for the laden absorbent, a liquid draw in the bottom of the regenerator and a gas draw in the top region of the regenerator; c) at least one top condenser connected to the gas draw of the regenerator, comprising a gas draw and a condensate outlet; and d) a distillation column comprising a condenser, an evaporator, a feed for the condensate outlet of the top condenser, a vapor draw in the top region of the column and a liquid draw at the bottom of the distillation column,

wherein the regenerator has a feed connected to the liquid draw at the bottom of the distillation column.

In a preferred embodiment, there is provided a process for separating an amine compound or a conjugate acid thereof and a carbamate compound or a conjugate acid thereof from a mixture having the amine compound, the carbamate compound, carbon dioxide and at least one anionic contaminant salt using an anionic exchange column, the process including passing the mixture through the column to obtain a first effluent and passing through the column an extraction fluid to obtain a second effluent, where the extraction fluid most preferably includes carbonic acid.

The invention relates to a process for removing hydrogen sulfide and carbon dioxide from a feed gas stream. H2S in the feed gas stream is converted to elemental sulfur in a Claus unit. At least a part of the gas stream obtained is contacted with an aqueous lean absorbing medium in an absorption zone at a pressure between 0.9 and 2 bara. The aqueous lean absorbing medium used comprises one or more amines chosen from: a polyamine in the absence of tertiary amine functionalities having a pKa sufficient to neutralize carbamic acid, the polyamine having at least one primary amine functionality having a pKa smaller than 10.0 at 25 C., a polyamine in the absence of tertiary amine functionalities having a pKa sufficient to neutralize carbamic acid, the polyamine having at least one secondary amine functionality having a pKa for each sorbing nitrogen smaller than 10.0 at 25 C. The process is improved as compared to a process involving Claus off-gas treatment with (activated) MDEA. Effective CO2 removal is achieved while at the same time a simplified line-up with less equipment can be used.