A minute cutting apparatus for a superabsorbent polymer hydrogel using a pump is disclosed. An embodiment of the present invention provides the minute cutting apparatus, including: a barrel body in which a transfer space through which the hydrogel is transferred is formed; a pumping unit installed in the barrel body to supply a pressing force to the transfer space, a rotation shaft rotatably installed in the transfer space of the barrel body; a driving motor configured to provide a rotational driving force to rotation shaft; a cutter member installed on the rotation shaft to pulverize the hydrogel transferred by the pressing force in the transfer space; and a perforated plate installed in the barrel body to discharge the hydrogel pulverized by the cutter member to an outside of the barrel body.

Disclosed is a method of decontamination by exposing a zirconium oxy(hydroxide) aerogel to a liquid, vapor, or gaseous sample suspected of containing a phosphonate compound. The aerogel may be doped with Fe.sup.3+ ions, Ce.sup.3+ ions, or SO.sub.4.sup.2− ions. The aerogel may be made by: providing a solution of ZrCl.sub.4; FeCl.sub.3, CeCl.sub.3, or Zr(SO.sub.4).sub.2; and a solvent; adding a cyclic ether to the solution to form a gel; infiltrating the gel with liquid carbon dioxide; applying a temperature and pressure to form supercritical fluid carbon dioxide; and removing the carbon dioxide for form an aerogel.

Provided is a water-absorbent resin which is capable of giving an absorbent material improved gel-shape stability and which has excellent water-absorption capacity. A water-absorbent resin of the present invention is a polymer of a water-soluble ethylenically unsaturated monomer, and has the following properties (1) and (2): (1) A disintegration amount at 20-fold swelling is 30% by mass or less; and (2) a solubility in physiological saline is 25% by mass or less. (Determination Method for Disintegration Amount at 20-Fold Swelling) 5 g of the water-absorbent resin is added to 100 g of physiological saline to allow the water-absorbent resin to absorb the physiological saline, thereby obtaining a gel. The obtained gel is divided approximately equally into five portions, and these portions are introduced respectively into cylindrical molds having a length of 3.6 cm and a radius of 2.8 cm and molded. The masses of the five molded cylindrical gels are measured. The heaviest and the lightest of the five gels are removed, and the remaining three gels are used as samples. A mass Wa (g) of each sample is measured. Each weighed sample is placed on the uppermost sieve of a combination of JIS standard sieves having a mesh size of 5.6 mm and a receptacle in this order and shaken for 10 minutes using a Ro-Tap shaker (rotation speed, 290 rpm; number of taps, 165 rpm). A mass Wb (g) of the gel which has passed through the sieves is measured. The disintegration amount of each sample is calculated using the following equation: Disintegration amount of sample (%)=Wb (g)/Wa (g)×100. An average of the disintegration amounts for three samples to be measured is regarded as the disintegration amount at 20-fold swelling of the water-absorbent resin.

Provided are sorption materials and devices using the sorption materials, and methods of using the sorption materials and devices containing the sorption materials. In various examples, the sorption materials bind to various inflammation stimulating and/or mediating molecules, which are often associated with systemic infections and systemic inflammation associated with conditions such as, for example, sepsis.

Disclosed are a superabsorbent polymer having improved anti-caking properties and a method of preparing the same, and the superabsorbent polymer having improved anti-caking properties includes a superabsorbent polymer, microparticles, and water, and to improve anti-caking properties of the superabsorbent polymer, the temperature of the superabsorbent polymer or water upon addition of water or the aging time upon stirring is adjusted, thereby preventing caking of the particles.

A method for preparing a super absorbent polymer and a superabsorbent polymer prepared from the same are disclosed herein. In some embodiments, a method includes mixing super absorbent polymer particles, water and an additive form a hydrated super absorbent polymer, wherein the super absorbent polymer particles comprise a base polymer powder including a cross-linked polymer polymerized from a water-soluble ethylenically unsaturated monomer having an acidic group of which at least a part is neutralized, and a surface cross-linked layer formed on the base polymer powder, wherein the surface cross-linked layer is formed by further cross-linking the cross-linked polymer, and wherein the additive including a polyoxyalkylene aliphatic hydrocarbon ether carboxylic acid. The method can appropriately control the water content of the super absorbent polymer by water-addition or the like to suppress crushing or the like during transfer, and also can suppress deterioration of physical properties.

A porous polymer aerogel, wherein the aerogel has greater than 5 wt % of amine containing vinyl monomers integrated into a polymer backbone. A method of fabrication of a porous polymer aerogel amine material, includes preparing a solution comprising at least a solvent, amine monomers having protected amino groups, one or more crosslinkers, one or more radical initiators, and a nitroxide mediator, removing oxygen from the solution, heating the solution to promote polymerization and to produce a polymerized material, performing solvent exchange with the polymerized material, causing a deprotection reaction in the polymerized material to remove groups protecting the amino groups, soaking and rinsing the material to remove excess reagents and any byproducts of the deprotection reaction, and drying the material to produce the amine sorbent. A system to separate CO2 from other gases, comprising a polymer porous aerogel sorbent having greater than 5 wt % of amine containing vinyl monomers integrated into a polymer backbone.

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 primary amine polymer aerogel comprising greater than 5 wt. % of primary amine monomers covalently bound to cross-linking monomers, wherein the primary amine monomers are selected from vinyl amine. A secondary amine polymer aerogel comprising secondary amine monomers covalently bound to cross-linking monomers, the secondary amine monomers being a result of substituting a hydrogen atom from a primary amine polymer aerogel, the primary amine polymer aerogel comprising vinyl amine monomers covalently bound to the cross-linking monomers. A tertiary amine polymer aerogel comprising tertiary amine monomers covalently bound to cross-linking monomers, the tertiary amine monomers being a result of substituting hydrogen atoms from a primary amine polymer aerogel, the primary amine polymer aerogel comprising vinyl amine monomers covalently bound to the cross-linking monomers.

Provided herein are methods, systems, and devices incorporating use of materials to store, ship, and deliver process gases to micro-electronics fabrication processes and other critical process applications.