A fiber comprising a carbon chain backbone and amidoxime, carboxylate, and nitrile pendant groups. The fiber may be used for removing uranium from seawater and toxic metals from drinking water.

Disclosed herein are hybrid membranes comprising: a microporous polymer, the microporous polymer comprising a continuous polymer phase permeated by a continuous pore phase; and an atomic scale inorganic material dispersed throughout the microporous polymer within the continuous pore phase. Methods of making and use of the hybrid membranes are also disclosed.

Chemically and thermally stable covalent organic framework (COF) materials are configured and operative as solid adsorbents for capturing gases and water.

The technology disclosed herein is directed to controlling humidity levels, such as the humidity level in an enclosed environment. The water isotherm of the adsorbent material is customized through the modification of the surface chemistry of the adsorbent. By modifying the surface chemistry of the adsorbent in various ways and to varying degrees, it is possible to customize the adsorbent properties to a range of different humidity levels. Such modification can enhance the adsorbing capacity and efficiency of the adsorbent, especially with regard to low molecular weight water-soluble compounds.

The present disclosure relates to a preparation method for a super absorbent polymer sheet and a super absorbent polymer sheet prepared therefrom. According to the preparation method of the present disclosure, a porous super absorbent polymer sheet can be prepared by a simplified process.

A method for the separation or depletion of empty AAV capsids from full AAV capsids in an aqueous mixture comprising empty and full AAV capsids, wherein the mixture is contacted with a primary amino groups bearing solid phase surface in a first alkaline milieu whereby (i) full AAV capsids bind to the solid phase surface whereas empty AAV capsids at least partially do not bind to the solid phase surface,
or (ii) both full and empty AAV capsids bind to the solid phase surface, and subsequently the empty AAV capsids are at least partially eluted by means of a second alkaline milieu of a pH value higher than the pH value of the first alkaline milieu, with the proviso that the second alkaline milieu does not elute full AAV capsids from the solid phase surface.

Disclosed is a microvesicles isolation method to isolate microvesicles contained in the biological sample from the sample, the method comprising: (a) adding an adsorbent sphere to the biological sample containing the microvesicles therein; (b) keeping the adsorbent sphere in the biological sample to form an adsorbent sphere conjugate composed of the adsorbent sphere and the microvesicles captured thereon; (c) isolating the adsorbent sphere conjugate from the biological sample; (d) washing the isolated adsorbent sphere conjugate using a first reagent; and (e) eluting the microvesicles from the washed adsorbent sphere conjugate using a second reagent, wherein the adsorbent sphere includes a support, and one or more polyvalent cations disposed on a surface of the support.

Mesoporous membranes have shown promising separation performance with a potential to lower the energy consumption, leading to a dramatic cost reduction. Recently, an extensive effort has been made on the design of membranes which brought a significant progress toward the synthesis of well-defined porous morphologies, most of which synthesized by surfactant-template methodology. Currently, the most well-designed state-of-the-art membranes using this technique are made from metals, polymers, carbon, silica, etc. In the present invention, we demonstrate mesoporous calcium-silicate particles having superior separation capacity and optimal permeability, thereby leading to reduced energy consumption for selective separation of gases/liquids and/or the combination thereof. We explore various methods to improve the calcium-silicate membranes properties by tuning pore density during the synthesis/aging process, while favoring the formation of uniformly distributed nanopores. Lowering particle density by controlling calcium to silicon ratio along with optimizing the surface area are essential in achieving our objective.

A metal adsorption acrylic fiber wherein the strontium adsorption rate is 85% or more when the strontium adsorption rate is measured using the following measurement method. A strontium adsorption rate measurement method (strontium 0.1 ppm measurement method) involves immersing a metal adsorption acrylic fiber into an immersion fluid, collecting the immersion fluid as a testing solution 24 hours after beginning the immersion, analyzing the quantity of strontium in the testing solution, obtaining the concentration (C.sub.1) (ppm) of strontium in the testing solution, creating a contrast solution, analyzing the quantity of strontium in the contrast solution as in the case with the testing solution, obtaining the concentration (C.sub.2) (ppm) of strontium in the contrast solution, and calculating the strontium adsorption rate of the metal adsorption acrylic fiber by using the following equation: strontium adsorption rate (%)={(C.sub.2−C.sub.1)/C.sub.2}×100.

The present invention relates to an odor control material consisting of a water-insoluble particulate odor control agent and a thermoplastic water-soluble carrier matrix encapsulating the odor control agent. The carrier matrix dissolves when in contact with an aqueous solution, such as urine and the odor control material is obtained by means of thermoforming. The invention relates also to a method for the preparation of the odor control material and the use of the odor control material in absorbent products. The present odor control material minimizes dusting problems caused by particulate odor control agents in production processes.