A platform and system for concentration, reduction and regeneration of heavy metals and other contaminants from fluids is provided. The platform has a three-tiered hierarchical porous structure, composed of micropores formed by woven carbon cloth, nanopores formed after carbon nanotube growth on the cloth fibers and mesopores formed by a polymer outer layer. The material of the platform can be incorporated into cells with two electrodes with properly functionalized PDAN grafted 3D carbon as an anode and cathode respectively. Metal ions and toxic anions in water will be captured selectively by primary amine, secondary amine and quaternary amine groups in porous PDAN on the anode. Metals are captured and reduced by the cathode.

A particulate plug for removing a preservative from a solution, suspension, or emulsion comprising a drug is presented. The plug comprises microparticles of a hydrophobic polymer/fatty acid blend. The microparticles of hydrophobic polymer/fatty acid blend selectively absorb preservative allowing the drug to remain in solution for delivery.

The present invention provides a process for preparing a functionalised polymeric chromatography medium, which process comprises (I) providing two or more non-woven sheets stacked one on top of the other, each said sheet comprising one or more polymer nanofibres, (II) simultaneously heating and pressing the stack of sheets to fuse points of contact between the nanofibres of adjacent sheets, and (III) contacting the pressed and heated product with a reagent which functionalises the product of step (II) as a chromatography medium.

The present invention relates to a method to improve chromatography beads. More closely, the invention relates to a novel method for production of dextran-containing porous media and chromatography media produced with this method. In the method, the chromatography media is subjected to dextranase-treatment leading to improved pressure-flow properties of the media.

An object of the present invention is to provide a ligand-immobilized sea-island composite fiber in which generation of fine particles due to peeling of a sea component from an island component and generation of fine particles due to destruction of a fragile sea component are both suppressed. The present invention provides a sea-island composite fiber comprising a sea component and island components, in which a value (L/S) obtained by dividing the average total length (L) of the perimeter of all island components in a cross section perpendicular to the fiber axis by the average cross-sectional area (S) of the cross section is from 1.0 to 50.0 μm.sup.−1, a distance from the surface to the outermost island component is 1.9 μm or less, and an amino group-containing compound is covalently bonded to a polymer constituting the sea component at a charge density of 0.1 μmol or more and less than 500 μmol per 1 gram dry weight.

Composite granules that contain a binder and polymeric sorbent materials for capturing reactive gases are provided. Additionally, methods of making the composite granules and methods of using the composite granules to capture reactive gases, and compositions formed by exposing the composite granules to reactive gases are provided. The polymeric sorbent material included in the composite granules is a reaction product of a divinylbenzene/maleic anhydride precursor polymeric material with a nitrogen-containing compound. This reaction results in the formation of nitrogen-containing groups that are covalently attached to the polymeric sorbent. The reactive gases undergo an acid-base reaction with the nitrogen-containing groups.

The present disclosure relates to lignocellulosic materials comprising phosphorylated lignocellulosic fibers having an ionic charge in water of about 4000 to about 7000 mmoles/kg, and processes for the preparation thereof. The process comprises reacting lignocellulosic fibers of a lignocellulosic material with a phosphate ester in the presence of urea. The present disclosure further relates to compositions comprising a phosphate ester and at least one of a defoamer and a viscosity reducer or at least one of a C1-C12 alcohol and an ester of a carboxylic acid.

A preparation method of a resin-based iron oxide-containing composite phosphate removal adsorbent is provided. An alkaline anion resin is taken as a base, a potassium ferrate is used as an iron source, and a characteristics of ferrate ions easily adsorbed on a surface of the anion resin are utilized to prepare resin-based iron oxide-containing composite phosphate removal adsorbent by one-step in-situ hydrolysis precipitation, compared with the related art, a preparation process of the disclosure is relatively simpler, a time period is shorter, and a production cost is lower. It has a strong ability to eliminate interference from other anions in the waste effluents, and it has a strong adsorption capacity, fast adsorption speed and large adsorption capacity for the phosphate. Moreover, it has the advantages of strong regeneration ability and multiple repeated use times.

A core-shell type amine-based carbon dioxide adsorbent is described, including a chelating agent resistant to oxygen and sulfur dioxide, to inhibit oxidative decomposition of amine. As a core, a porous support is employed on which an amine compound is immobilized, and, as a shell, an amine layer resistant to inactivity by sulfur dioxide is utilized. Such adsorbent exhibits high oxidation resistance because the chelating agent functions to remove a variety of transition metal impurities catalytically acting on amine oxidation. In addition, the sulfur dioxide-resistant amine layer of the shell selectively adsorbs sulfur dioxide to protect the amine compound of the core and, at the same time, the amine compound of the core selectively adsorbs only carbon dioxide. Sulfur dioxide adsorbed on the shell is readily desorbable therefrom at about 110° C. and thus remarkably improved regeneration stability is obtained during temperature-swing adsorption (TSA) processes in which sulfur dioxide is present.

A gas detection unit is accommodated within a housing of a gas sensor and the outside atmosphere of the housing is introduced through the filter to the gas detection unit. The filter comprises an organic polymer gas-permeable filter removing siloxanes and an inorganic filter removing alcohols and passing gases to be detected.