Provided is the use of a carboxylate compound as an absorbent for capturing carbon dioxide and/or in the preparation of an absorbent for capturing carbon dioxide. In the carboxylate compound, the carboxylate anion is a carboxylate radical with a carbon chain having a carbon atom number of more than 3, or a branched-chain carboxylate radical having a carbon atom number of more than 6; and the cation is a substituted quaternary ammonium ion, quaternary phosphorus ion, pyridinium ion, pyrrolium ion, piperidinium ion, imidazolium ion or metal ion. In the present invention, a method which can capture carbon dioxide in an efficient and energy-saving manner by using a carboxylate compound and has water stability is involved, and the method comprises the following step: putting an aqueous solution of a carboxylate compound in a carbon dioxide atmosphere to absorb carbon dioxide, thereby obtaining a carboxylate and carbon dioxide conjugate precipitated from water.

The present application is directed to processes for removing carbon dioxide (CO.sub.2) from low CO.sub.2 concentration gaseous streams. The process comprises contacting the gaseous stream with a hydrogel for absorbing at least some CO.sub.2 from the gaseous stream. The hydrogel comprises a cross-linked hydrophilic polymer comprising a hydrophilic polymer cross-linked with a cross-linking agent. Processes for preparing the hydrogel, types of hydrogels, using the hydrogel to remove CO.sub.2 from gaseous streams, and regenerating the hydrogel to recover absorbed CO.sub.2 from the hydrogel are also disclosed.

An activated carbon device for adsorbing solvent from a flow of air is regenerated by feeding heated inert gas to the activated carbon and by applying a reduced pressure to the heated activated carbon.

A resin includes a functionalized aminopolymer having amine sites for capturing carbon dioxide molecules, where each aminopolymer molecule has at least one functional group amenable to crosslinking, a porogen, and a crosslinking initiator. A product includes an aminopolymer material formed into a self-supporting structure, the aminopolymer material including crosslinked aminopolymers having amine sites for the capture of carbon dioxide molecules.

Methods of designing zeolite materials for adsorption of CO.sub.2. Zeolite materials and processes for CO.sub.2 adsorption using zeolite materials.

An adsorption material is disclosed that comprises a metal-organic framework and a plurality of ligands. The metal-organic framework comprising a plurality of metal ions. Each respective ligand in the plurality of ligands is amine appended to a respective metal ion in the plurality of metal ions of the metal-organic framework. Each respective ligand in the plurality of ligands comprises a substituted 1,3-propanediamine. The adsorbent has a CO.sub.2 adsorption capacity of greater than 2.50 mmol/g at 150 mbar CO.sub.2 at 40° C. Moreover, the adsorbent is configured to regenerate at less than 120° C. An example ligand is diamine 2,2-dimethyl-1,3-propanediamine. An example of the metal-organic framework is Mg.sub.2(dobpdc), where dobpdc.sup.4− is 4,4′-dioxidobiphenyl-3,3′-dicarboxylate. Example applications for the adsorption material are removal of carbon dioxide from flue gas and biogasses.

A method of increasing hydrothermal stability of an adsorbent comprising a small pore cationic zeolite in a swing adsorption process is disclosed. The method comprises the steps of coating the zeolite with a silylation agent to result in a silylated zeolite; and performing the swing adsorption process. The swing adsorption process comprises contacting the silylated zeolite with feed stream comprising water. The swing adsorption process may comprise removing CO.sub.2 from a feed stream comprising CO.sub.2 and water.

The present invention relates to an organic-inorganic hybrid nanoporous material, maintaining a nanoporous skeleton structure formed by coordination of an organic ligand containing an aromatic compound to a trivalent central metal ion, and further having an intramolecular acid anhydride functional group modified on the aromatic compound of the nanoporous skeleton structure, and thereby exhibits selectivity for olefins, and an adsorbent comprising the same. Specifically, the organic-inorganic hybrid nanoporous material of the present invention exhibits an excellent olefin-selective adsorption capacity through differences in adsorption equilibrium and adsorption rate, and thus can be usefully employed in the separation of C2-C4 hydrocarbons. Further, the olefins adsorbed to the organic-inorganic hybrid nanoporous material can be desorbed by purging of an inert gas which is not liquefied by way of mild vacuum conditions or compression, and thus, the organic-inorganic hybrid nanoporous material can be used to prepare olefins by separating C2-C4 hydrocarbon mixtures.

A method and apparatus for removing a volatile component from a mixture are disclosed. The method and apparatus employ a crosslinked elastomer with a glass transition temperature ≤+25° C. as the sorbent.

The present disclosure relates to methods and systems for regenerating molecular sieves used in an alcohol dehydration process after the molecular sieves have become saturated with water.