Patent classifications
C08G75/23
PHOTORESIST COMPOSITION, LIQUID DISCHARGE HEAD AND LIQUID DISCHARGE HEAD MANUFACTURING METHOD
A photoresist composition is provided, which comprises a cationic polymerization resin, a resin A, a photoacid generator, and a solvent, wherein the resin A comprises at least one resin selected from the group consisting of polyester resins and polyether resins and is soluble in a ketone-based organic solvent.
PHOTORESIST COMPOSITION, LIQUID DISCHARGE HEAD AND LIQUID DISCHARGE HEAD MANUFACTURING METHOD
A photoresist composition is provided, which comprises a cationic polymerization resin, a resin A, a photoacid generator, and a solvent, wherein the resin A comprises at least one resin selected from the group consisting of polyester resins and polyether resins and is soluble in a ketone-based organic solvent.
BIO-BASED SULFONE COPOLYMERS FREE OF BPA AND BPS
A bio-based poly(arylether sulfone) copolymer (“copolymer b-PAES”) comprises at least two sulfone recurring units derived from two distinct dihydroxy/diol monomers: a bio-compatible and bio-based diol momoner and a bisphenol monomer distinct from Bisphenol S (BPS) and Bisphenol A (BPA). The dihydroxy bisphenol monomer comprises a substituted-phenol bisphenolic compound distinct from BPS and BPA, preferably comprises a bisphenol F derivative with both alkyl substituted-phenol groups. The bio-based diol monomer comprises at least one diol selected from isosorbide, isomannide and/or isoidide. The copolymer b-PAES is preferably free of BPA and BPS. A process for manufacturing such copolymer b-PAES, its use for manufacturing an article, an article made therefrom such as membranes, and a polymer solution for manufacture of membrane comprising such copolymer b-PAES.
BIO-BASED SULFONE COPOLYMERS FREE OF BPA AND BPS
A bio-based poly(arylether sulfone) copolymer (“copolymer b-PAES”) comprises at least two sulfone recurring units derived from two distinct dihydroxy/diol monomers: a bio-compatible and bio-based diol momoner and a bisphenol monomer distinct from Bisphenol S (BPS) and Bisphenol A (BPA). The dihydroxy bisphenol monomer comprises a substituted-phenol bisphenolic compound distinct from BPS and BPA, preferably comprises a bisphenol F derivative with both alkyl substituted-phenol groups. The bio-based diol monomer comprises at least one diol selected from isosorbide, isomannide and/or isoidide. The copolymer b-PAES is preferably free of BPA and BPS. A process for manufacturing such copolymer b-PAES, its use for manufacturing an article, an article made therefrom such as membranes, and a polymer solution for manufacture of membrane comprising such copolymer b-PAES.
Fluorinated copolymer composition
A fluorinated copolymer composition includes a thermoplastic resin A and a fluorinated elastomer B dispersed within thermoplastic resin A. Thermoplastic resin A has a shear stress (τ.sub.A) of greater than 0.11 MPa when measured with a capillary rheometer at a shear rate of 243 sec.sup.−1 and at 360° C. in accordance with ASTM D3835. Fluorinated elastomer B dispersed within thermoplastic resin A has an average dispersed particle size of less than 50 μm.
ARTICLE/PART COMPRISING A POLYMERIC COMPONENT AND A METALLIC COATING
The invention pertains to a article or a part, comprising: —a first layer (1) of a composition (C) comprising a polymeric component comprising a) at least one poly(aryl ether ketone) polymer (PAEK), and b) at least one poly(aryl ether sulfone) polymer (PAES), wherein the composition (C) further comprises glass fibers and/or carbon fibers and has a melting temperature (Tm) of at least 290° C., as measured by differential scanning calorimetry (DSC) according to ASTM D3418, and—at least one coating (2) of metal having a thickness of at least 20 μm, preferably at least 30 μm. The present invention also relates to a process for preparing this article/part by metallisation and to the use of such articles and parts in electrical & electronic applications, mobile electronics, smart devices & wearables and smart phones.
PROTECTIVE LAYER FOR PROTECTING LITHIUM METAL NEGATIVE ELECTRODE FOR LITHIUM SECONDARY BATTERY, PRODUCTION METHOD THEREOF, AND LITHIUM SECONDARY BATTERY INCLUDING THE SAME
Disclosed is a protective layer to protect a lithium metal negative electrode for a lithium secondary battery, in which the protective layer may inhibit formation of lithium dendrite and improve thermal/chemical stability, and conductivity of lithium ions. Further, disclosed are a production method of the protective layer, and a lithium secondary battery including the protectively layer. The protective layer contains a poly(arylene ether sulfone)-poly(ethylene glycol) graft copolymer represented by a following Chemical Formula 1:
##STR00001## where, in the Chemical Formula 1, n is an integer of 60 to 80, and m is an integer of 40 to 45.
END-CAPPED POLY(ARYL ETHER SULFONE) POLYMERS, POLY(ARYL ETHER SULFONE) BLOCK COPOLYMERS, AND CORRESPONDING SYNTHESIS METHODS
Described herein are end-capped poly(aryl ether sulfone) (“PAES”) polymers and corresponding synthesis methods. The end-capped PAES polymers are end-capped by functionalizing a PAES polymer with a halophthalic diialkyl ester end-capping agent. It was surprisingly discovered that the resulting dialkyl phthalate end-capped PAES polymers could be synthesized with significantly improved end-capping conversion rates, relative to end-capped PAES polymers directly functionalized with traditional phthalic anhydride end-capping agents. It was also surprisingly found that by heating the isopropyl phthalate end-capped PAES polymers, the polymers could be converted to the corresponding phthalic anhydride end-capped PAES polymers, yielding a more efficient synthetic route to phthalic anhydride end-capped PAES polymers.
END-CAPPED POLY(ARYL ETHER SULFONE) POLYMERS, POLY(ARYL ETHER SULFONE) BLOCK COPOLYMERS, AND CORRESPONDING SYNTHESIS METHODS
Described herein are end-capped poly(aryl ether sulfone) (“PAES”) polymers and corresponding synthesis methods. The end-capped PAES polymers are end-capped by functionalizing a PAES polymer with a halophthalic diialkyl ester end-capping agent. It was surprisingly discovered that the resulting dialkyl phthalate end-capped PAES polymers could be synthesized with significantly improved end-capping conversion rates, relative to end-capped PAES polymers directly functionalized with traditional phthalic anhydride end-capping agents. It was also surprisingly found that by heating the isopropyl phthalate end-capped PAES polymers, the polymers could be converted to the corresponding phthalic anhydride end-capped PAES polymers, yielding a more efficient synthetic route to phthalic anhydride end-capped PAES polymers.
POLYMERIC INSULATING FILMS
Insulating films suitable for use in magnet wire, electrical machines, and other applications may include at least one layer formed from extruded material. The extruded material may include a blend of a first polymeric material and a second polymeric material different than the first polymeric material. The first polymeric material may include one of polyetheretherketone, polyaryletherketone, polyetherketoneketone, polyphenylsulfone, polyphenylene sulfide, or polybenzimidazole, and the second polymeric material may include one of polyphenylsulfone, polyetherimide, polyethersulfone, polyphenylene sulfide, polycarbonate, or polyester.