A method and an integrated system for reducing CO.sub.2 emissions in industrial processes. The method and integrated system (100) capture carbon dioxide (CO.sub.2) gas from a first gas stream (104) with a chemical absorbent to produce a second gas stream (106) having a higher concentration of carbon monoxide (CO) gas and a lower concentration of CO.sub.2 gas as compared to first gas stream. The CO gas in the second gas stream is used to produce C.sub.5 to C.sub.20 hydrocarbons in an exothermic reaction (108) with hydrogen (H.sub.2) gas (138). At least a portion of the heat generated in the exothermic reaction is used to regenerate the chemical absorbent with the liberation of the CO.sub.2 gas (128) captured from the first gas stream. Heat captured during the exothermic reaction can, optionally, first be used to generate electricity, wherein the heat remaining after generating electricity is used to thermally regenerate the chemical absorbent.

A system for carbon dioxide capture from a gas mixture comprises a lean solvent comprising 3-amino-1-propanol (AP), 2-dimethylamino-2-methyl-1-propanol (DMAMP), and water; an absorber containing at least a portion of the lean solvent, wherein the absorber is configured to receive the lean solvent and a gaseous stream comprising carbon dioxide, contact the lean solvent with the gaseous stream, and produce a rich solvent stream and a gaseous stream depleted in carbon dioxide; a stripper, wherein the stripper is configured to receive the rich solvent stream; a cross-exchanger fluidly coupled to a rich solvent outlet on the absorber and a rich solvent inlet on the stripper; a reboiler fluidly coupled to a lower portion of the stripper; and a condenser fluidly coupled to a vapor outlet of the stripper.

An absorption liquid regeneration apparatus includes: a regeneration tower for regenerating a CO.sub.2 absorption liquid; a reflux water drum configured to separate released gas from the regeneration tower into CO.sub.2 gas and condensed water, and return the condensed water to the regeneration tower; and a cleaning part installed in a gas-phase part of the reflux water drum or in a CO.sub.2 flow passage through which the CO.sub.2 gas having flowed from the gas-phase part flows, and configured to remove a CO.sub.2 absorption agent contained in the CO.sub.2 gas by using a cleaning liquid. The cleaning liquid has a lower concentration of the CO.sub.2 absorption agent than the condensed water stored in a liquid-phase part of the reflux water drum.

A reclaiming apparatus includes: a container in which reclaiming process of an absorption liquid is performed; a waste liquid line configured through which a waste liquid from the container flows; a waste liquid cooler, installed in the waste liquid line, for cooling the waste liquid from the container; and a cleaning-water supply line for supplying the waste liquid cooler with cleaning water for cleaning the waste liquid cooler.

A CO.sub.2 recovery apparatus includes: an absorption tower configured to remove CO.sub.2 in an exhaust gas by contacting with a CO.sub.2 absorption liquid containing an absorption agent; a regeneration tower for regenerating the CO.sub.2 absorption liquid from the absorption tower; a reflux water drum for separating CO.sub.2 gas released from the regeneration tower into CO.sub.2 gas and condensed water; a first cleaning device installed in a gas-phase part of the regeneration tower and configured to remove the absorption agent contained in the CO.sub.2 gas flowing through the gas-phase part, by using a first cleaning liquid containing at least the condensed water from the reflux water drum or a water obtained from the condensed water; and a control device configured to adjust a supply amount of the first cleaning liquid to the first cleaning device so that a concentration of the absorption agent in the condensed water is maintained to be not greater than a predetermined value.

An aqueous CO2 absorbent comprising a combination of 2-amino-2-methyl-1-propanol (AMP) and 3-aminopropanol (AP), or AMP and 4-aminobutanol (AB), is described. A method for capturing CO2 from a CO2 containing gas using the mentioned absorbent, and the use of a combination of AMP and AP, or a combination of AMP and AB are also described.

The embodiments provide an acidic gas absorbent, an acidic gas removal method, and an acidic gas removal apparatus. The absorbent absorbs an acidic gas in a large amount and hardly diffuses in air. The acidic gas absorbent according to the embodiment comprises an amine compound having a sulfonyl group and two or more amino groups.

The present invention is related to a method for determination of unit operations of a chemical plant for acid gas removal, the method carried out by a computer or a distributed computer system and the method comprising the steps of: providing a first set of parameters for the unit operations; providing a second set of parameters for the unit operations based on the provided first set of parameters and based on data retrieved from a database; determining a digital model of the chemical plant based on the first set of parameters and the second set of parameters, wherein the digital model comprises a system of equations defining the unit operations of the chemical plant; selecting starting points for an equation-based solution method of the system of equations, wherein the starting points are at least partially selected from the: (i) the first set of parameters; (ii) the second set of parameters; and (iii) the data retrieved from the database; determining resultant settings for the unit operations of the chemical plant using the equation-based solution method for the system of equations initialized by the selected starting points.

The present invention relates to methods for improving carbon capture by providing particles within an amine solvent. The particles provide for increased turbulence at the interface between the counter-flowing gas and solvent, which allows for increased amine and carbamate salt diffusion between the liquid film and bulk.

An improved process for deacidizing a gaseous mixture with reduced overall energy costs is described. The process involves contacting the gaseous mixture with at least one of a vaporizing compound, a vaporized compound, a vaporizing solution of compound and a vaporized solution of compound, and forming a liquid or solid reaction product that can be easily separated from the gaseous mixture.