The present invention relates to a superabsorbent polymer and a method for producing the same. The superabsorbent polymer includes a core layer polymerized with monomers having carboxylic group, a first shell layer formed from a surface crosslinking agent, and a second shell layer formed from zingiberaceae extracts. By a surface modification on the first shell layer performed from a specific amount of the zingiberaceae extracts, the superabsorbent polymer produced according to the method for producing the same has a good antimicrobial property and deodorizing effects, and retains an original absorbent property.

The present invention relates to sulfur based polymers and a process of making sulfur based polymers. The invention also relates to sorbents comprising the sulfur-based polymers. The invention also relates to the use of such polymers and sorbents in metal remediation or extraction. The invention also relates to methods of removing heavy metals from fluids.

The present disclosure generally relates to a scalable, green process for producing non-toxic, all-cellulose super absorbent hydrogels that form instantly after cross-linking. A super absorbent hydrogel can be produced by physical mixing of water-soluble carboxyalkyl polysaccharides such carboxymethyl cellulose and negatively-charged cellulose nanocrystals resulting in instantaneous gelation. Cellulose nanocrystals act as effective cross-linkers when physically mixed with carboxymethyl cellulose in an aqueous medium. The resulting hydrogel possesses excellent absorption properties, and has applications in a wide range of products from hygiene products to medical and industrial super absorbent products.

Solid phase extraction (SPE) sorbents and liquid chromatography (LC) stationary phases are provided, as well as methods of fabricating the same. The SPE sorbents and LC stationary phases can use microcrystalline cellulose particles as the substrate and sol-gel sorbent coating technology as the polymer/sorbent immobilization technology. The SPE sorbents and LC stationary phases are stable in a pH range of 1-13 and at a temperature of up to 350° C.

Devices and methods related to a chitosan-enhanced melamine sponge are provided. A method comprises grafting chitosan on the melamine sponge matrix via the chemical with two or more carboxyl groups; and crosslinking the chitosan with crosslinker under a heating procedure to make a more robust melamine sponge with a larger surface and smaller pores. The chitosan-enhanced melamine sponge is used to separate chemicals from water as a gravity flow-driven filter, and it can be compressed and backwashed for regeneration.

Construction for absorbing a fluid, for example, a liquid or gaseous, organic chemical, has an extended web, fabric, yarn or foam member and associated with the extended web, fabric, yarn or foam member is a water-insoluble polymer. The water-insoluble polymer can absorb the fluid organic chemical, and the construction provides for contact of the water-insoluble polymer with the fluid organic chemical when deployed in an environment where the fluid organic chemical may be present for absorption. The construction may be employed in aquatic, aqueous, or dry environments, as a blotter, a wipe or sponge, a filter, in a cartridge, and so forth.

Construction for absorbing a fluid, for example, a liquid or gaseous, organic chemical, has an extended web, fabric, yarn or foam member and associated with the extended web, fabric, yarn or foam member is a water-insoluble polymer. The water-insoluble polymer can absorb the fluid organic chemical, and the construction provides for contact of the water-insoluble polymer with the fluid organic chemical when deployed in an environment where the fluid organic chemical may be present for absorption. The construction may be employed in aquatic, aqueous, or dry environments, as a blotter, a wipe or sponge, a filter, in a cartridge, and so forth.

A composition and method for recovery and/or bioremediation of oil spills and/or hydrophobic hydrocarbons includes (a) cellulosic material, (b) a charged polymer adsorbed to the cellulosic material, and optionally (c) microorganisms combined with the polymer and/or cellulosic material.

Supported amine polymer adsorbents based on polymers containing only or primarily primary amines sites are to be used as regenerable adsorbents for CO.sub.2 capture from ultra-dilute gas streams, such as ambient air, or from mixtures of gases containing preferably at least 10% oxygen. and can also be useful for use at the moderate gas pressures found in typical post-combustion capture processes, such as flue gas from large point sources such as coal-fired power plants. Preferred supported solid amine adsorbents of this invention are based on poly(allylamine) (“PAA”) and poly(vinyl amine) (“PVAm”), both of which are linear polymers, and their derivatives, containing substantially all primary amine groups, supported on substrates. Preferred such substrates include silica mesocellular foam (MCF) and mesoporous-γ-alumina, as well on mesoporous-γ-alumina coated throughout the pores of MCF, most preferably of monolithic structure. Preferred derivatives include the guanidinylated and cross-linked poly(allylamine) materials.

The present invention relates to a super-absorbent polymer having excellent properties, both centrifugal retention capacity (CRC) and absorption under pressure (AUP) having been improved by introducing a surface crosslinked layer crosslinked by surface-modified inorganic particles, and to a method for preparing the same. The super-absorbent polymer comprises: a base resin powder containing a crosslinked polymer of water-soluble ethylene-based unsaturated monomers having an at least partially neutralized acidic group; and a surface crosslinked layer formed on the base resin powder, wherein inorganic particles may be chemically bound to the crosslinked polymer contained in the surface crosslinked layer, via an oxygen-containing bond or a nitrogen-containing bond.