Disclosed are a carbon dioxide absorbent composition in which an N-alkylaminoalkanol; a polyhydroxyamine-based compound; and ethylenediamine and/or diethylenetriamine are mixed, a method for preparing the same, and a method and an apparatus for carbon dioxide absorption/separation using the same. Since the carbon dioxide absorbent according to the present disclosure has superior carbon dioxide absorption capacity and remarkably lower absorbent recycling temperature as compared to the existing absorbents such as monoethanolamine, etc., total energy consumption in the capturing process can be reduced greatly. In addition, since carbon dioxide is recovered at low recycling temperature, contamination by water or absorbent vapor may be prevented.

An aspect of the present invention is a gas treatment method including: an absorption step of bringing a gas to be treated, which contains carbon dioxide and a sulfur compound, into contact with an absorption liquid to be phase-separated by carbon dioxide absorption, to cause the absorption liquid to absorb the carbon dioxide and the sulfur compound; and a first release step of heating the absorption liquid brought into contact with the gas to be treated to a temperature equal to or higher than a temperature at which the carbon dioxide absorbed by the absorption liquid is released from the absorption liquid and lower than a temperature at which the sulfur compound absorbed by the absorption liquid is released from the absorption liquid, to release the carbon dioxide from the absorption liquid.

Methods and compositions useful, for example, for physical solvent carbon capture. The solvents may include an aqueous mixture of 2-amino-2-methylproponol, 2-piperazine-1-ethylamine, diethylenetriamine, 2-methylamino-2-methyl-1-propanol, and potassium carbonate or potassium carbonate buffer salt. The solvent may also contain less than about 75% by weight of dissolving medium (i.e., water) and may have a single liquid phase. The solvents and methods have favourable regeneration energies, chemical stability, vapour pressure, total heat consumption, net cyclic capacity, and reaction kinetics.

A system for scrubbing and monitoring H2S includes: a sample inlet valve that controls an input stream of the hydrocarbon gas from the gas canister; a first scrubber that removes a first portion of H2S from the input stream and that outputs a first stream with less H2S than the input stream; a second scrubber that removes a second portion of H2S from the first stream and that outputs a second stream with less H2S than the first stream; a H2S converter that converts all remaining H2S in the second stream into a di-ketone and that outputs an output stream with a concentration of the di-ketone; an optical detector that measures the concentration of the di-ketone in the output stream; and a processor that determines a concentration of H2S in the second stream based on the concentration of the di-ketone in the output stream.

The present invention relates to a biocompatible task specific hybrid solvent (TSHS) composition that synergistically increases the carbon capture efficiency and utilizes less energy for CO.sub.2 desorption over the existing solutions. Further, the process of synthesizing such composition is discussed in this disclosure. Also, the present disclosure provides a process that involves a task specific hybrid solvent (TSHS) composition for selective capturing CO.sub.2 from any gaseous stream.

There is provided a polymer or derivative thereof comprising a plurality of active amine groups in the backbone, wherein the polymer is a reaction product of a reaction between one or more bis-carbonates and one or more amine compounds having at least two terminal amino groups. Also provided are use of the polymer or derivative thereof and a method of preparing the polymer or derivative thereof.

Hydrogen sulfide is removed from a gas stream by bubbling a gas stream having ≥100 ppm hydrogen sulfide through a scavenging mixture. The scavenging mixture includes: 1) at least one sweetener selected from the group consisting of triazines, oxazolidines, hemiacetals, and mixtures thereof, and 2) at least one reaction catalyst selected from the group consisting of dipropyl amine (DPA), diethyl amine (DEA), dimethyl amine (DMA), pyrrole, and mixtures thereof. The scavenging mixture interacts with the hydrogen sulfide to produce a cleaned gas stream having ≤ 5 ppm hydrogen sulfide.

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 aqueous solvent composition is provided, comprising a nucleophilic component having one or more sterically unhindered primary or secondary amine moieties, a Brønsted base component having one or more basic nitrogen moieties, a water-soluble organic solvent, and water. A biphasic composition is provided, comprising one or more carbamate compounds, one or more conjugate acids of Brønsted base, a water-soluble organic solvent, and water. A biphasic CO.sub.2 absorption process is also provided, utilizing the biphasic solvent composition.

The present invention relates to a process for removing acid compounds contained in a gaseous effluent which consists in bringing a gaseous effluent into contact, in the absorption column, with an absorbent solution comprising water, between 20% and 28% by weight of pentamethyldipropylenetriamine and between 5% and 35% by weight of N-methyldiethanolamine.