A porous activated asphaltene material is described with a method of making and a method of using for the adsorption of a contaminant from a solution. The porous activated asphaltene material may be made by functionalizing solid asphaltene with nitric acid, and then treating the product with a metal hydroxide. The resulting porous activated asphaltene material exhibits a high porosity, and may be cleaned and reused for adsorbing contaminants.

A polymer/activated carbon composite made up of a branched polyethylenimine and magnetic cores involving Fe.sub.3O.sub.4 disposed activated carbon. The magnetic cores have activated carbonyl groups on the surface. A process for removing organic dyes, such as methyl red, as well as heavy metal ions from a polluted aqueous solution or an industrial wastewater utilizing the composite is introduced. A method of synthesizing the polymer/activated carbon composites is also specified.

An aminated siliceous adsorbent, which is the reaction product of dried acidified rice husk ash having disordered mesopores and an amino silane, wherein amine functional groups are present on an external surface and within the mesopores of the dried acidified rice husk ash, and wherein the aminated siliceous adsorbent has a carbon content of 24 to 30 wt. %, based on a total weight of the aminated siliceous adsorbent. A method of making the aminated siliceous adsorbent and a method of capturing CO.sub.2 from a gas mixture with the aminated siliceous adsorbent.

In various embodiments, the present disclosure pertains to core-shell particles that comprise a porous hybrid organic-inorganic shell disposed on a surface-modified non-porous polymer particle core. In some embodiments, the present disclosure pertains to chromatographic separation devices that comprise such core-shell particles. In some embodiments, the present disclosure pertains to chromatographic methods that comprise: (a) loading a sample onto a chromatographic column comprising such core-shell particles and (b) flowing a mobile phase through the column.

Macroporous desiccant based honeycomb matrix containing the macroporous desiccant synthesized “in-situ”, the desiccant having a differential water adsorption. Process for the “in-situ” preparation of the macroporous desiccant based honeycomb matrix including the steps of soaking honeycomb substrate impregnated with water glass, in aqueous metal salt(s) solution or acid solution, or combination thereof, until such time that the hydrogel honeycomb matrix is obtained and thermally activating the hydrogel honeycomb matrix to produce macroporous desiccant based honeycomb matrix.

The invention relates to a method to produce a particulate activated carbon material for capturing CO.sub.2 from air, wherein the particulate activated carbon is impregnated with alkali carbonate salt such as K.sub.2CO.sub.3; and wherein the impregnated particulate activated carbon either has, determined using nitrogen adsorption methods, a pore volume of at least 0.10 cm.sup.3/g for pore sizes of at least 5 nm and a pore volume of at most 0.30 cm.sup.3/g for pore sizes of less than 2 nm or is based on a mixture of different alkali carbonate salts, or has a particular pore surface for pore sizes in the range of 2 nm-50 nm.

Lime-based sorbent suitable for use in a flue gas treatment process comprising at least 70 wt. % of Ca(OH).sub.2 and at least 0.2 wt. % to at most 10 wt. % of a first additive selected among the group of hydrogels of natural or synthetic origin, in particular superabsorbent polymers (SAPs) or in the group of cellulose ethers or a combination thereof, premix for use in a manufacturing process of said sorbent, process for manufacturing the sorbent and use of said sorbent in a flue gas treatment process

A lithium ion adsorbent includes a material having a chemical formula of LiCl.2Al(OH).sub.3.nH.sub.2O. n is an integer from 1 to 3, a specific surface area of the lithium ion adsorbent is 20-36 m.sup.2/g, an average pore diameter of the lithium ion adsorbent is 20-35 nm, a total pore volume of the lithium ion adsorbent is 0.15-0.32 mL/g, a D10 of the lithium ion adsorbent is 3-12 μm, a D50 of the lithium ion adsorbent is 12-22 μm, and a D90 of the lithium ion adsorbent is 20-40 μm.

The present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for its preparation and separations devices containing the chromatographic material; separations devices, chromatographic columns and kits comprising the same; and methods for the preparation thereof. The chromatographic materials of the invention are chromatographic materials comprising having a narrow particle size distribution.

A coated substrate (2a, 2b) adapted for hydrocarbon adsorption having at least one surface, and a coating on the at least one surface, the coating comprising particulate carbon and a binder, wherein the particulate carbon has a BET surface area of at least about 1300 m.sup.2/g; and at least one of: (i) a butane affinity of greater than 60% at 5% butane; (ii) a butane affinity of greater than 35% at 0.5% butane; (iii) a micropore volume greater than about 0.2 ml/g and a mesopore volume greater than about 0.5 ml/g. A bleed emission scrubber (1) and an evaporative emission control canister system (30) comprising the coated substrate (2a, 2b) are provided. They can control evaporative hydrocarbon emissions and may provide low diurnal breathing loss (DBL) emissions even under a low purge condition.