A flexible substrate, a manufacturing method thereof, and a flexible display device are provided. The method includes: step S10, forming a first aerogel layer with a cross-linked structure and a nanoporous structure on a substrate; step S20: forming an inorganic layer on the first aerogel layer; step S30, forming a second flexible substrate layer on the first aerogel layer, and allowing the second flexible substrate layer to cover the inorganic layer; and step S40, peeling the first aerogel layer, the inorganic layer, and the second flexible substrate layer from the substrate to form the flexible substrate.

The present invention is intended to provide a laminated film including a void-provided layer achieving both a high proportion of void space and a high film strength. The laminated film of the present invention includes a void-provided layer 21 and a resin film 10, the void-provided layer 21 being stacked on the resin film 10. The laminated film is produced by a production method, including steps of forming a void-provided structure 20′, which is a precursor of the void-provided layer 21 on the resin film; and causing a crosslinking reaction in the precursor 20′ after the precursor forming step. The precursor 20′ contains a substance that generates a basic substance by light irradiation or heating, the basic substance is not generated in the precursor forming step, the basic substance is generated by light irradiation or heating in the crosslinking reaction step, and the crosslinking reaction step has multiple stages.

Disclosed are micronized hydrophilic systems of highly concentrated, cross-linked biopolymers. The system is created by combining a biopolymer with a cross-linking agent under mechanical kneading and allowing the biopolymer to undergo a cross-linking process followed by purification, drying and milling. The resulting micronized biopolymer system has an increased biopolymer concentration and increased longevity within the body.

The present invention relates to a method for crosslinking hyaluronic acid, a method for preparing an injectable hydrogel, the hydrogel thus obtained and its use.

A karst channel type water inrush efficient-blocking ultra-high expansion grouting material, preparation, methods and application thereof, the grouting material includes macromolecule polymer particles A and a cross-linking solidifying fluid B, wherein the macromolecule polymer particles A are an inlaid type core-shell structure, primary macromolecule water-absorbent resin serves as an inner core, part of a gelling catalyzer is attached to an the inner core surface forming a shell, and the gelling catalyzer permeates the inner core forming an inlaid structure; before use, the macromolecule polymer particle A and the cross-linking solidifying fluid B are stirred; and then obtained mixed liquid is used as the grouting material to be injected into a fracture of a rock mass fracture zone. By means of the grouting material, high-pressure large-flow karst water inrush can be efficiently treated, the blocking efficiency of water inrush is improved, and major underground engineering construction of China is further facilitated.

A cured elastomer golf ball component is made by heating an elastomer compound containing an ethylenically unsaturated elastomer, an ethylenically unsaturated monomer, and first and second free radical initiators to a first crosslinking temperature T.sub.1 in a compression mold and partially crosslinking the elastomer, then heating to a second crosslinking temperature T.sub.2 and curing the elastomer component of the golf ball. Either: (i) the first initiator has a half-life of about 0.2-5 minutes at T.sub.1, the second initiator has a half-life of about 0.2-5 minutes at T.sub.2, and T.sub.2 is higher T.sub.1 by at least about 30° C.; or (ii) the second initiator's one-minute half-life temperature is at least about 30° C. higher than the first initiator's one-minute half-life temperature, T.sub.1 is within about 20° C. of the first initiator's one-minute half-life temperature, and T.sub.2 is within about 20° C. of the second initiator's one-minute half-life temperature.

The disclosure provides recording materials including propane derivatized monomers and polymers for use in volume Bragg gratings, including, but not limited to, volume Bragg gratings for holography applications. Several structures are disclosed for propane derivatized monomers and polymers for use in Bragg gratings applications, leading to materials with higher refractive index, low birefringence, and high transparency. The disclosed propane derivatized monomers and polymers thereof can be used in any volume Bragg gratings materials, including two-stage polymer materials where a matrix is cured in a first step, and then the volume Bragg grating is written by way of a second curing step of a monomer.

An autohesive polymer material that includes: at least one polymer having at least two terminal silyl groups of the Formula (1) given by:
Si(R.sup.1).sub.a(R.sup.2).sub.b  (1).
Each of the radicals R.sup.1 comprises an alkyl, alkenyl or aryl group or a hydrogen atom. Each of the radicals R.sup.2 comprises a group that can be eliminated with water, b is 1, 2 or 3, and a is 3−b. The polymer material further includes at least one condensation catalyst. Further, the polymer material is chemically precrosslinked and further crosslinkable with moisture. In addition, the polymer material is configured for use as a layer body that can be applied to a substrate. The polymer material of this kind can also be used for producing permanent bonds.

An epoxy resin B-stage film obtained by semi-curing an epoxy resin composition, the epoxy resin composition including: a liquid crystalline epoxy monomer capable of forming a cured product that includes a liquid crystal structure; and a curing agent, in which the epoxy resin B-stage film has an average thickness of less than 8 μm, and in which the liquid crystal structure included in the cured product turns into a liquid crystal structure, in which molecules are orientated in a film thickness direction, by being cured.

High performance electrodes for electrochemical devices having a polymer network with an electroactive material chemically attached to a crosslinked polymer matrix are disclosed. A method includes mixing an electrode slurry and forming a polymer network within the electrode slurry. The electrode slurry includes an electroactive material, an electrically conductive filler, a plurality of polymer chains, and a plurality of chemical crosslinking precursors. Each chemically crosslinking precursor is configured to (i) chemically crosslink the plurality of polymer chains and (ii) chemically attach the electroactive material to the plurality of polymer chains.