Patent classifications
C08G75/0227
High Molecular Weight Polyphenylene Sulfide Resin, Preparation Method and Use Thereof
A sulfur-containing compound and a halogenated aromatic compound are used as raw materials, with an alkaline compound and a fatty acid as polycondensation aids to carry out a polycondensation reaction. After purification treatment, a primary polyphenylene sulfide is obtained which then reacts with a chain extender at high temperature to form a high molecular weight polyphenylene sulfide resin. A preparation method has the advantages of being high yield, low cost, and capable of selectively and controllably preparing polyphenylene sulfide resins with different melt viscosities and molecular weights, and the obtained polyphenylene sulfide resins have excellent heat resistance. The linear high molecular weight polyphenylene sulfide resin with high thermal stability can be used for producing plates, pipes and rods, can be mechanically processed like metals, such as cutting, grinding, polishing, drilling, and can be used to produce fibers, membranes, films, and are applicable to automotive parts, electronic/electrical equipment, chemical and machinery.
POLY(ARYLENE SULFIDE) POLYMERS AND CORRESPONDING POLYMER COMPOSITIONS AND ARTICLES
Described herein are poly(arylene sulfide) (“PAS”) polymers (PASP) including recurring units formed from selected dihalofluorene monomers. Surprisingly, at relative low dihalofluorene monomer concentrations, the PAS polymers (PASP) have significantly increased glass transition temperatures (“T.sub.g”) and impact performance, relative to analogous PAS homopolymers and PAS polymers (PASP) including recurring units formed from 4,4′-dibromobiphenyl (“DBBP”). Simultaneously, the PAS polymers (PASP) also retain high elastic modulus. Furthermore, the PAS polymers (PASP) are free of recurring units formed from polyhalogenated biphenyls (e.g. DBBP and polychlorinated biphenyls) and, therefore, are not currently subject to restrictive governmental regulation. Due at least in part to the excellent thermal (T.sub.g, T.sub.c and T.sub.m) and impact properties of the PAS polymers (PASP), the PAS polymers (PASP) and PAS polymer compositions can be desirably incorporated into wide variety of articles including, but not limited to, automotive articles, electrical and electronic articles, articles for aerospace and oil and gas articles.
POLY(ARYLENE SULFIDE) POLYMERS AND CORRESPONDING POLYMER COMPOSITIONS AND ARTICLES
Described herein are poly(arylene sulfide) (“PAS”) polymers (PASP) including recurring units formed from selected dihalofluorene monomers. Surprisingly, at relative low dihalofluorene monomer concentrations, the PAS polymers (PASP) have significantly increased glass transition temperatures (“T.sub.g”) and impact performance, relative to analogous PAS homopolymers and PAS polymers (PASP) including recurring units formed from 4,4′-dibromobiphenyl (“DBBP”). Simultaneously, the PAS polymers (PASP) also retain high elastic modulus. Furthermore, the PAS polymers (PASP) are free of recurring units formed from polyhalogenated biphenyls (e.g. DBBP and polychlorinated biphenyls) and, therefore, are not currently subject to restrictive governmental regulation. Due at least in part to the excellent thermal (T.sub.g, T.sub.c and T.sub.m) and impact properties of the PAS polymers (PASP), the PAS polymers (PASP) and PAS polymer compositions can be desirably incorporated into wide variety of articles including, but not limited to, automotive articles, electrical and electronic articles, articles for aerospace and oil and gas articles.
OPTICAL POLYMER AND LENS INCLUDING SAME
A lens includes an optical unit, and a rib unit extending outwardly in a radial direction of the optical portion, wherein the rib unit includes a light transmitting region and a light blocking region, and the light blocking region is disposed in the rib unit.
OPTICAL POLYMER AND LENS INCLUDING SAME
A lens includes an optical unit, and a rib unit extending outwardly in a radial direction of the optical portion, wherein the rib unit includes a light transmitting region and a light blocking region, and the light blocking region is disposed in the rib unit.
POLYVINYL THIOETHER ESTER, PREPARATION METHOD THEREFOR AND USE THEREOF.
Disclosed are a polyvinyl thioether ester, a preparation method therefor and use thereof. The polyvinyl thioether ester is obtained by subjecting a binary acetylenic acid ester-based internal-alkyne monomer and a dithiol monomer as starting materials to a solution polymerization reaction. The staring materials of the polymerization reaction are easy to obtain, and no by-products are produced during the process of the polymerization reaction. The polymerization reaction has a wide substrate applicability and a good functional group compatibility, such that various functional groups can be conveniently introduced. No catalyst is used in the polymerization reaction, and, the influence of a catalyst residue on the optical and electrical properties and the biological properties of a polymer material can be eliminated. The prepared polyvinyl thioether ester has a good workability, a higher heat stability and aggregation-induced luminescence performance, and has application value in terms of optical plastics, biomedical materials, fluorescent sensing, etc.
Crosslinked polymers and related compositions, electrochemical cells, batteries, methods and systems
Crosslinked polymers and related compositions and related compositions, electrochemical cells, batteries, methods and systems are described. The crosslinked polymers have at least one redox active monomeric moiety having a redox potential of 0.5 V to 3.0 V with reference to Li/Li.sup.+ electrode potential under standard conditions or −2.54 V to −0.04 V vs. SHE and has a carbocyclic structure and at least one carbonyl group or a carboxyl group on the carbocyclic structure. The crosslinked polymers also include at least one comonomeric moiety with at least one of the at least one redox active monomeric moiety and/or the at least one comonomeric moiety has a denticity of three to six corresponding to a three to six connected network polymer, and provide stable, high capacity organic electrode materials.
Highly hydrophobic antifouling coatings for implantable medical devices
Antibacterial coatings and methods of making the antibacterial coatings are described herein. In particular, a method for forming an organocatalyzed polythioether coating is provided in which a first solution including a bis-silylated dithiol and a fluoroarene is prepared. A second solution including an organocatalyst is prepared. The first solution and the second solution are mixed to form a mixed solution. The mixed solution is applied to a substrate, and the substrate is cured.
Highly hydrophobic antifouling coatings for implantable medical devices
Antibacterial coatings and methods of making the antibacterial coatings are described herein. In particular, a method for forming an organocatalyzed polythioether coating is provided in which a first solution including a bis-silylated dithiol and a fluoroarene is prepared. A second solution including an organocatalyst is prepared. The first solution and the second solution are mixed to form a mixed solution. The mixed solution is applied to a substrate, and the substrate is cured.
Polyarylene sulfide resin, method for producing same, poly(arylene sulfonium salt), and method for producing poly(arylene sulfonium salt)
Disclosed is a production method comprising a step of obtaining a poly(arylene sulfonium salt) comprising a terminal group including at least one functional group selected from the group consisting of a carboxy group, a hydroxy group and an amino group, and a step of dealkylating or dearylating the poly(arylene sulfonium salt) to obtain a polyarylene sulfide resin, and a polyarylene sulfide resin comprising a terminal group including a functional group obtainable by the production method.