Provided is a water-absorbing agent having an excellent ability to absorb and retain liquid and an excellent liquid suction power. The water-absorbing agent contains a polyacrylic acid (salt)-based water-absorbing resin as a main component and satisfies all of the following physical properties (a) to (e): (a) a weight average particle diameter (D50) is 300 μm or more and less than 400 μm; (b) a proportion of particles with a particle diameter of 600 μm or more and less than 850 μm is less than 10 weight %; (c) an average gap radius is 100 μm or more and less than 180 μm; (d) a CRC is 28 g/g or more and less than 34 g/g; and (e) an AAP is 24 g/g or more.

A filter bag is disclosed that comprises a porous membrane having a strength in the transverse direction to improve durability. There is a filter assembly for filtering particulates from a gas stream comprising a support substructure and a filter bag at least partially surrounding the support substructure. The filter bag comprises a porous membrane having a upstream surface exposed to the gas stream. The porous membrane is lightweight and has a structure to collect the particulates on the upstream surface. In particular, the porous membrane has a bubble point of 0.06 MPa or more and has a strength in a transverse direction that is 100 N/m or more. Other filter bags disclosed comprise a laminate comprising a porous membrane having a bubble point of 0.06 MPa or more and a second layer that acts as a sacrificial material.

A substrate includes a double-network polymer system including a cross-linked, covalently-bonded polymer and a reversible, partially ionicly-bonded polymer, wherein the substrate has a moisture level less than or equal to 15 percent of the total weight of the substrate, wherein the substrate is porous, and wherein the substrate includes a latent retractive force. A method for manufacturing a substrate includes producing a double-network hydrogel including a cross-linked, covalently-bonded polymer and a reversible, ionicly-bonded polymer; elongating by force the double-network hydrogel in at least one direction; treating the double-network hydrogel with an organic solvent with a volatile and water-miscible organic solvent to replace a majority of water within the double-network hydrogel; evaporating the organic solvent while the double-network hydrogel is still elongated to form a substantially-dried double-network polymer system; and releasing the force to produce the substrate.

A magnetic polymer adsorption material, preparation method and use thereof, which relate to the field of magnetic polymer materials. The preparation method comprises: (1) preparing magnetic nanoparticles; (2) dissolving the magnetic nanoparticles in a pore-forming agent, adding N-vinylpyrrolidone, divinylbenzene and an initiator respectively, and mixing uniformly; (3) adding an emulsifier and a dispersant into an aqueous solution; adding a part of the oil phase solution prepared in step (2) at the temperature below 60° C., and adding the rest of the oil phase solution when the temperature rises to 60° C. or above, reacting with stirring, precipitating and filtering the reacted solution, washing and drying the precipitate, and finally obtaining the magnetic polymer adsorption material. The material has the particle size of 2-100 μm, the magnetization of 5-19.5 emu/g and the specific surface area of 210-950 m.sup.2/g, and can be applied to the adsorption of inorganic and organic matters in solutions, the controlled release of inorganic and organic matters, and the separation of different substances.

A magnetic polymer adsorption material, preparation method and use thereof, which relate to the field of magnetic polymer materials. The preparation method comprises: (1) preparing magnetic nanoparticles; (2) dissolving the magnetic nanoparticles in a pore-forming agent, adding N-vinylpyrrolidone, divinylbenzene and an initiator respectively, and mixing uniformly; (3) adding an emulsifier and a dispersant into an aqueous solution; adding a part of the oil phase solution prepared in step (2) at the temperature below 60° C., and adding the rest of the oil phase solution when the temperature rises to 60° C. or above, reacting with stirring, precipitating and filtering the reacted solution, washing and drying the precipitate, and finally obtaining the magnetic polymer adsorption material. The material has the particle size of 2-100 μm, the magnetization of 5-19.5 emu/g and the specific surface area of 210-950 m.sup.2/g, and can be applied to the adsorption of inorganic and organic matters in solutions, the controlled release of inorganic and organic matters, and the separation of different substances.

Polymer sorbents selectively remove cytokines and bacterial endotoxins from whole blood and other body liquids, in particular blood plasma, lymph etc., as well as from aqueous protein solutions and aqueous organic compound solutions, also containing inorganic salts. The sorbent is able to remove both cytokines and bacterial endotoxins, improve selectivity of the polymer sorbents in respect to the compounds as well as provide a simple and effective method of producing said sorbent.

Provided are: a water-absorbing agent achieving, in a balanced manner, both good physical properties and a decrease in speed of coloration with lapse of time even if the water-absorbing agent has a high moisture absorbing speed due to having a large specific surface area; and an absorbent body having a low ratio of pulp and achieving, in a balanced manner, both good physical properties suitable for a thin disposable diaper and a decrease in speed of coloration with lapse of time. The absorbent body contains a hydrophilic base material and a water-absorbing agent which contains: surface-crosslinked water-absorbing resin particles having a non-uniformly pulverized shape; α-hydroxycarboxylic acid (salt); and an aminocarboxylic acid-based chelating agent and/or a phosphorus-based chelating agent, a point plotted along an x-axis that represents an amount (x.sub.1 mol %) of α-hydroxycarboxylic acid (salt) extracted from the water-absorbing agent and along a y-axis that represents an amount (y.sub.1 mmol %) of an aminocarboxylic acid-based chelating agent and/or a phosphorus-based chelating agent extracted from the water-absorbing agent being within a range that satisfies a specific relational formula of x.sub.1 and y.sub.1, the water-absorbing agent having a moisture absorbing speed of 120 mg/g/hr or more at a temperature of 40±1° C. at a relative humidity of 75±1% RH.

The present disclosure relates to a preparation method for a super absorbent polymer film. Specifically, it relates to a preparation method for a new type of super absorbent polymer film, which is thin and exhibits excellent absorption performance. In addition, the super absorbent polymer film of the present disclosure has excellent flexibility and excellent mechanical properties, is free from scattering or leaking, and does not require an auxiliary substance such as pulp, so that products can be made thinner and the manufacturing process and costs may be reduced.

A hollow fiber membrane module includes: a first hollow fiber membrane whose sieving coefficient for dextran having a molecular weight of not less than 300 kDa nor more than 1000 kDa is not less than 0.12 nor more than 0.28, wherein the first hollow fiber membrane adsorbs endotoxins.

In various embodiments, the present disclosure pertains to organic polymer core-shell particles that comprise a non-porous organic polymer core (i.e., having a pore volume of less than 0.1 cc/g) and a porous organic polymer shell (i.e., having a pore volume of greater than 0.1 cc/g), in which the porous organic polymer shell has a pore size ranging from 100 Å to 3000 Å. In some embodiments, the present disclosure pertains to chromatographic separation devices that comprise such organic polymer 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 organic polymer core-shell particles and (b) flowing a mobile phase through the column.