A method of producing an ion-conducting membrane containing a polymer having an ionic group, involves multiple liquid treatment steps in which a precursor membrane is brought into contact with an acid treatment solution or an alkali treatment solution, the precursor membrane containing a polymer in a state in which the aforementioned ionic group forms a salt with an impurity ion, wherein the liquid treatment time in the second and subsequent liquid treatment steps of the multiple liquid treatment steps is shorter than the liquid treatment time in the initial liquid treatment step.

Cure monitoring systems for and methods of monitoring polymerizable material to determine the degree of curing of the polymerizable material. A monitoring light source delivers visible monitoring light at one or more different visible wavelengths and a visible light detector detects the monitoring light diffusely reflected by the polymerizable material. The monitoring light has a wavelength of maximum emission (max-mon) that does not effectively induce polymerization of the polymerizable material. Change in intensity of the monitoring light reflected from the polymerizable material is used to determine when a selected degree of curing is reached in the polymerizable material.

A display apparatus and a method of manufacturing a display apparatus, the apparatus including a substrate; a display on the substrate; and an encapsulation layer that seals the display, wherein the encapsulation layer includes a matrix including an organic material, and an inorganic material bonded to the organic material through functional groups of the organic material of the matrix, wherein the matrix includes an internal space adjacent to the organic material, the inorganic material being positioned in the internal space.

Although polyolefin elastomers are widely employed commodity polymers, there are shortcomings of this class of polymers for certain applications. For example, the rheological properties of some polyolefin elastomers may be insufficient to provide the green strength or low shear viscosity necessary to form stable foams, or to provide sufficient viscosity modification effects when present in a solvent. Cationomeric modification of polyolefin elastomers may alleviate these difficulties. Such polyolefin elastomers may feature a random cationomeric polyolefin copolymer comprising at least a first monomer and a second monomer, in which the first monomer is a neutral monomer and the second monomer has a side chain bearing a cationic moiety. The polyolefin elastomers may be present in foamed polyolefin compositions comprising a gas component and/or in liquid compositions comprising a solvent in which the polyolefin elastomer is dissolved.

Modified polyvinyl alcohol contains a (meth)acrylamide monomer unit having an ionic group, wherein the modified polyvinyl alcohol has a degree of saponification of from 50 to 99.99 mol % and a viscosity-average degree of polymerization of from 200 to 5000 and satisfies formulae (1) to (3) below. The modified polyvinyl alcohol thus obtained is particularly excellent in dispersibility in water.
0.8(Mw.sub.UV/Mw.sub.RI)1.3(1)
1(Mw.sub.UV/Mn.sub.UV)7(2)
0.03A.sub.2800.5(3).

The present invention relates to a ligand-containing conjugated microporous polymer, which is obtained by covalent coupling of a conjugated microporous polymer and a uranium complexing ligand. The conjugated microporous polymer comprises an aromatic ring and/or a heterocyclic ring. The uranium complexing ligand is selected from the group consisting of a compound with a group containing phosphorus, a compound with a group containing nitrogen, and a compound with a group containing sulfur. The invention further provides use of the ligand-containing conjugated microporous polymer as a uranium adsorbent. The ligand-containing conjugated microporous polymer the invention is capable of adsorbing the radioactive element uranium in strongly acidic and strong-radiation environments.

Scorch of a silane-functionalized polyolefin is minimized during melt mixing with a flame retardant through the use of a polydimethylsiloxane (PDMS) having a (1) number average molecular weight (Mn) greater than or equal to () 4,000 grams per mole (g/mol), (2) viscosity of greater than or equal to () 90 centipoise (cP), and (3) hydroxyl group content of less than or equal to () 0.9 weight percent (wt %) based on the weight of the PDMS.

[Problem] To provide a gel which can be produced in a short time, has controlled properties such as modulus and expansion pressure, and has a low polymer concentration. [Solution] A process for producing a polymer gel in which gel-precursor clusters have been crosslinked with one another to form a three-dimensional network structure, characterized by comprising a) a step in which monomer or polymer units that are present in a concentration less than a critical gelation concentration are crosslinked to form the gel-precursor clusters, the gel-precursor clusters having a storage modulus G and a loss modulus G which satisfy the relationship G<G, and b) a step in which the gel-precursor clusters are crosslinked with one another by a crosslinking agent to obtain a gel having a three-dimensional network structure.

The present invention relates to a porous organic polymer-based hydrogen ion conductive material and a method for preparing the same. More specifically, the present invention relates to a method for preparing a porous organic polymer (POP)-based material with high proton conductivity that is applicable to a membrane electrode assembly (MEA) of a proton exchange membrane fuel cell (PEMFC). The porous organic polymer-based proton conductive material of the present invention can be prepared in an easy and simple manner by microwave treatment and acid treatment requiring short processing time and low processing cost. In addition, the porous organic polymer-based proton conductive material of the present invention can be developed into a highly proton conductive material having the potential to replace Nafion through a simple post-synthesis modification. Therefore, the porous organic polymer-based proton conductive material of the present invention is suitable for use in a proton exchange membrane fuel cell.

The present disclosure provides methods and processes for the recovery of compounds (e.g., pendant groups) from polymeric materials, as well as methods for recycling and reusing such compounds by synthetically converting a recovered compound to building blocks that can be used in, e.g., curable resins for the fabrication of new devices, such as medical devices (e.g., orthodontic appliances).