The invention is directed to a nanostructured composite material comprising a mixture of at least one metal particle such as iron and a carbon material from biomass such as D-glucose, D-glucosamine hydrochloride or a-cyclodextrin. The invention is also directed to a composition comprising the composite material comprising the composite material and an inorganic salt, and a method for synthesizing the composite material comprising immersing the carbon material into a solution of metal ions, drying the impregnated carbon particle and subjecting the impregnated carbon particle to a carbothermal reduction process. The nanostructured composite material is useful as an oxygen scavenging layer in a multi-layer film which comprises the oxygen scavenging layer and an oxygen barrier layer that retards the permeation of oxygen from an external environment.

The invention concerns high-performance adsorbents based on activated carbon of high meso- and macroporosity which are present in the form of discrete grains of activated carbon, wherein: at least 55% of the total pore volume of the high-performance adsorbents are formed by pores (i.e. meso- and macropores) having pore diameters of more than 20 , the high-performance adsorbents have a measure of central tendency pore diameter of more than 25 , and the high-performance adsorbents have a BET surface area of at least 1250 m.sup.2/g.

These high-performance adsorbents are obtainable by a novel process comprising specific two-stage activation, and have, in addition to the aforementioned properties, an excellent abrasion and bursting resistance, so that they are useful for a multiplicity of different applications.

Provided are a method of preparing a metal oxide-silica composite aerogel, which includes preparing metal oxide-silica composite precipitates by adding a metal salt solution to a silicate solution and performing a reaction, and washing the metal oxide-silica composite precipitates with a washing solvent having a surface tension at 205 C. of 30 mN/m or less and drying the washed metal oxide-silica composite precipitates, and a metal oxide-silica composite aerogel having increased specific surface area and pore properties as well as tap density, which is significantly reduced by a maximum of 78.6% in comparison to a composite aerogel prepared by using water as a typical washing solvent, prepared by the method.

The present disclosure provides a macroporous noble metal catalyst and processes employing such catalysts for the regeneration of deactivated ionic liquid catalyst containing conjunct polymer.

Disclosed is a pharmaceutical composition for treating hyperuricemia (HUA). The pharmaceutical composition includes a polysaccharide-polyamine copolymer and a pharmaceutically acceptable salt thereof as active ingredients. The polysaccharide-polyamine copolymer is formed by copolymerization of the following two parts: a selectively oxidized polysaccharide with 2,3-dialdehydo, and a polyamine with an amino functional group; the polyamine with an amino functional group and the selectively oxidized polysaccharide with 2,3-dialdehydo can form a net structure by means of covalent crosslinking, resulting in a hydrogel with an amino functional group or a granular polysaccharide-polyamine copolymer, wherein the amino functional group in the hydrogel with an amino functional group or the granular polysaccharide-polyamine copolymer can be protonated so as to form a cationic copolymer of a three-dimensional network structure having a protonated site, and the nitrogen content of the cationic copolymer and the nitrogen content of the polysaccharide-polyamine copolymer are above 12.3 wt %, and both the cationic copolymer and the polysaccharide-polyamine copolymer are water-insoluble.

Provided are graft copolymer particles enabling introduction of adsorptive functional groups adsorbing metals and others, a method for producing same, and an adsorbent using same. (1) Porous graft copolymer particles containing graft chains introduced into porous particles (particle surface having an average pore diameter of 0.01-50 ?m) including at least one resin selected from olefin resins, water-insoluble modified polyvinyl alcohol resins, amide resins, cellulosic resins, chitosan resins and (meth)acrylate resins. (2) A method for producing porous graft copolymer particles including (I) melt-kneading a polymer A and a polymer B other than the polymer A to obtain a compound material, (II) extracting and removing the polymer B from the compound material to obtain a porous material of the polymer A, (III) granulating the porous material, and (IV) introducing graft chains into the porous particles. (3) An adsorbent of porous graft copolymer particles.

A method is disclosed for the separation of ethane and heavier hydrocarbons or propane and heavier hydrocarbons from natural gas to provide a methane-rich natural gas stream and less volatile natural gas liquids (NGLs). This method provides for the use of a regenerable adsorbent media comprising a porous cross-linked polymeric adsorbent, a pyrolized macroporous polymer, or mixtures thereof, which is regenerated by a pressure swing adsorption (PSA) process, temperature swing adsorption (TSA) process, or combination of the two. Said regeneration step may be operated as a batch process, a semi-continuous process, or preferably as a continuous process.

A fluid purification system capable of removing lead from significant volumes of fluids also containing at least one of TOC and TTHM under low pressure conditions and at reasonable flow rates is provided. The system comprises a first fluid purification media comprising a rigid porous purification block. The rigid purification block includes a longitudinal first surface; a longitudinal second surface disposed inside the longitudinal first surface; and a porous high density polymer disposed between the longitudinal first surface and the longitudinal second surface. The system further includes a second fluid purification media, comprising a fibrous, nonwoven fabric disposed adjacent to the first surface of the first fluid purification media, the second surface of the first purification media, or both.

Covalently cross-linked copolymers are described herein. More specifically, polysaccharide-polyamine copolymeric matrices or structures and cationic copolymeric matrices are described herein. The polysaccharide-polyamine copolymers, when protonated, can form cationic copolymeric matrices having exceptionally high densities of cationic sites. In one form, the covalently cross-linked copolymers provide a three-dimensional structure, especially when hydrated.

The present disclosure relates to a composition for use in a gas storage vessel, said composition comprising at least two MOF monolithic bodies, including at least about 50 wt % of a first MOF monolithic body, and a second MOF monolithic body. The MOF monolithic bodies contain MOF and binder. The first MOF monolithic body has a volume of macropores of about 15% or less of the envelope volume of the first MOF monolithic body, a particle aspect ratio of about 2 or greater and a smallest particle diameter of greater than or equal to about 1 mm. The second MOF monolithic body has a largest particle diameter about equal to or less than the smallest particle diameter of the first MOF monolithic body.