A solvent comprised of (1) a caustic and an alcohol, (2) a caustic and a quaternary ammonium hydroxide, or (3) a caustic, an alcohol, and a quaternary ammonium hydroxide may contact an adsorbent bed that has been used to remove sulfur compounds from a hydrocarbon stream to extract adsorbed sulfur compounds from the adsorbent material in the bed to regenerate it. The regenerated adsorbent bed may be reused, either alone or in combination with a liquid-liquid extraction column, to remove sulfur compounds from a hydrocarbon stream.

A method for separating mixed xylene includes steps that the mixed xylene is subjected to adsorption separation by means of an adsorbent having a metal organic framework material, so that one or more of xylene isomers are separated out. An organic ligand in the metal organic framework material is 2,5-dihydroxy-1,4-benzoquinone. Xylene isomers can be effectively separated using this method.

An adsorption apparatus and associated method for capturing an target gaseous adsorbate from an atmospheric air based gaseous feed stream. The adsorption apparatus comprises: a housing enclosing at least one adsorption element for adsorbing the target gaseous adsorbate, the at least one adsorption element comprising at least one substrate coated with an adsorptive composite coating that comprises at least 50 wt % metal organic framework and at least one binder, the housing having an inlet through which the gaseous feed stream can flow to the adsorption element and an outlet through which gas can flow out from the housing; and a desorption arrangement in contact with and/or surrounding the at least one adsorption element, the desorption arrangement being selectively operable between (i) a deactivated state, and (ii) an activated state in which the arrangement is configured to heat, apply a reduced pressure or a combination thereof to the adsorptive composite coating to desorb at least a portion of the adsorbed target gaseous adsorbate from the adsorptive composite coating.

Process for converting waste plastics to refining feedstock. The process includes conducting pyrolysis of a plastic feedstock comprising waste plastics to produce a liquid stream of plastic pyrolysis oil; directly feeding the liquid stream of plastic pyrolysis oil to an adsorption based purification process to generate a treated plastic pyrolysis oil stream; and collecting the treated plastic pyrolysis oil stream from the adsorption vessel for further processing into value added products as a feedstock for conventional refining processes. The adsorption based purification process includes contacting the liquid stream of plastic pyrolysis oil with one or more adsorbent materials in an adsorption vessel, the adsorbent materials with at least one of the one or more adsorbent materials being configured for adsorption of organic molecules having heteroatoms of each of sulfur, nitrogen, oxygen, and chlorine. Such system may be integrated with a conventional refinery.

An example method of removing hydrogen sulfide from an input gas includes exposing an adsorbent material to an input gas to obtain an output gas. A concentration of hydrogen sulfide of the output gas is less than a concentration of hydrogen sulfide of the input gas. The adsorbent material includes copper oxide, magnesium oxide, and aluminum oxide. An atomic ratio of copper to magnesium to aluminum of the adsorbent material is X:Y:Z, where X is greater than or equal to 0.6 and less than or equal to 0.9, where Y is greater than or equal to 0 and less than or equal to 0.2, where Z is greater than or equal to 0 and less than or equal to 0.2, and where X+Y+Z is equal to 1.

A method of treating a metal carbonate salt includes hydrolyzing a metal halide salt to form a hydrohalic acid and a hydroxide salt of the metal in the metal halide salt. The metal includes an alkaline earth metal or an alkali metal. The method includes reacting the hydrohalic acid with the metal carbonate salt, wherein the metal carbonate salt is a carbonate salt of the alkaline earth metal or alkali metal, to form CO.sub.2 and the metal halide salt. At least some of the metal halide salt formed from the reacting of the hydrohalic acid with the metal carbonate salt is recycled as at least some of the metal halide salt in the hydrolyzing of the metal halide salt to form the hydrohalic acid and the hydroxide salt.

Oleophilic-hydrophobic-magnetic (OHM) porous materials are provided. In embodiments, an OHM porous material comprises a porous substrate having a solid matrix defining a plurality of pores distributed through the solid matrix, the OHM porous material further comprising a coating of a nanocomposite on surfaces of the solid matrix. The nanocomposite comprises a multilayer stack of a plurality of layers of a two-dimensional, layered material having nucleation sites interleaved between a plurality of layers of magnetic nanoparticles, wherein individual layers of magnetic nanoparticles in the plurality of layers of magnetic nanoparticles are each directly anchored on a surface of a layer of the plurality of layers of the two-dimensional, layered material via the nucleation sites, and are each separated by multiple layers of the plurality of layers of the two-dimensional, layered material. Methods of making and using the OHM porous materials are also provided.

To provide an immunoglobulin purification method which achieves a high immunoglobulin recovery percentage without causing loss of the antibody nature of an immunoglobulin. The immunoglobulin purification method includes an adsorption step and a desorption step. The adsorption step involves adsorption of an immunoglobulin onto porous zirconia particles in a neutral buffer. The desorption step involves desorption of the immunoglobulin adsorbed on the porous zirconia particles from the porous zirconia particles by means of a neutral desorption liquid.

A composite material for use in water treatment. The composite material includes a porous matrix including a resin capable of retaining a catalyst and magnetic material therein, and includes a density regulating portion disposed therein. The catalyst is capable of facilitating a chemical reaction involving a contaminants in the water. The magnetic material and density regulating portion can be used to separate the composite material from treated water. Systems and methods of use involving passive water treatment, continuous water treatment, solar light exposure, UV light exposure, and electrochemical cells, employing photochemical, electrochemical, and photoelectrochemical reactions are described. Methods of manufacture are described.

A method for manufacturing a carbon dioxide adsorbent includes preparing an amine aqueous solution having an amine compound concentration ranging from 5% to 70% inclusive and a temperature ranging from 10° C. to 100° C. inclusive, impregnating silica gel with the amine aqueous solution, and aeration-drying the silica gel carrying the amine compound. The silica gel has a particle size ranging from 1 mm to 5 mm inclusive, an average pore diameter ranging from 10 nm to 100 nm inclusive, and a pore volume ranging from 0.1 cm.sup.3/g to 1.3 cm.sup.3/g inclusive.