C08G75/23

COPOLYMER HAVING FUNCTIONAL GROUP AS SUBSTITUENT AT CHAIN-END, METHOD FOR PREPARING ELECTROLYTE MEMBRANE FOR SECONDARY BATTERY INCLUDING THE SAME, AND ELECTROLYTE MEMBRANE FOR SECONDARY BATTERY INCLUDING THE SAME

Disclosed is a copolymer as PAES-g-PEG or PAEK-g-PEG as an arylene-based polymer having ion conductivity and mechanical strength and having a functional group as a substituent at a chain-end of PEG, wherein the functional group includes one selected from a group consisting of a hydroxyl group (—OH), methacrylate (-MA), a double hydroxyl group (-2OH), a nitrile group (—CN) and an ionic liquid group (-PYRTFSI). Further, disclosed is a solid electrolyte membrane for a secondary battery including the copolymer and thus having improved ion conductivity, lithium ion transport ability, and excellent mechanical strength.

COPOLYMER HAVING FUNCTIONAL GROUP AS SUBSTITUENT AT CHAIN-END, METHOD FOR PREPARING ELECTROLYTE MEMBRANE FOR SECONDARY BATTERY INCLUDING THE SAME, AND ELECTROLYTE MEMBRANE FOR SECONDARY BATTERY INCLUDING THE SAME

Disclosed is a copolymer as PAES-g-PEG or PAEK-g-PEG as an arylene-based polymer having ion conductivity and mechanical strength and having a functional group as a substituent at a chain-end of PEG, wherein the functional group includes one selected from a group consisting of a hydroxyl group (—OH), methacrylate (-MA), a double hydroxyl group (-2OH), a nitrile group (—CN) and an ionic liquid group (-PYRTFSI). Further, disclosed is a solid electrolyte membrane for a secondary battery including the copolymer and thus having improved ion conductivity, lithium ion transport ability, and excellent mechanical strength.

Tröger's base-linked poly(crown ethers)s

Described herein are double-strand chain compositions suitable for use in the preparation of proton conductive membranes. The double-strand chains comprise a plurality of constitutional units joined to each other through two atoms on one side of the constitutional unit and two atoms on the other side of the constitutional unit. Constitutional units comprise a dibenzo-crown ether macrocycle fused with a bicyclic aliphatic linker. Polymers, membranes, and fuel cells comprising the double-strand chain are also described herein.

Tröger's base-linked poly(crown ethers)s

Described herein are double-strand chain compositions suitable for use in the preparation of proton conductive membranes. The double-strand chains comprise a plurality of constitutional units joined to each other through two atoms on one side of the constitutional unit and two atoms on the other side of the constitutional unit. Constitutional units comprise a dibenzo-crown ether macrocycle fused with a bicyclic aliphatic linker. Polymers, membranes, and fuel cells comprising the double-strand chain are also described herein.

AROMATIC POLYSULFONE RESIN, EPOXY RESIN COMPOSITION, PREPREG, AND MOLDED BODY
20220073682 · 2022-03-10 ·

An aromatic polysulfone resin produced by the polycondensation of 4,4′-dihydroxydiphenylsulfone represented by chemical formula (S1) shown below and 2-(4-(4-hydroxyphenylsuIfonyl)phenoxy)-5-(4-hydroxyphenylsulfonyl)phenol represented by chemical formula (S2) shown below with 4,4′-dichlorodiphenylsulfone represented by chemical formula (S3) shown below.

##STR00001##

wherein hydrogen atoms in phenylene groups in formula (S1), formula (S2) and formula (S3) may be each independently substituted with an alkyl group, an aryl group or a halogen atom.

AROMATIC POLYSULFONE RESIN, EPOXY RESIN COMPOSITION, PREPREG, AND MOLDED BODY
20220073682 · 2022-03-10 ·

An aromatic polysulfone resin produced by the polycondensation of 4,4′-dihydroxydiphenylsulfone represented by chemical formula (S1) shown below and 2-(4-(4-hydroxyphenylsuIfonyl)phenoxy)-5-(4-hydroxyphenylsulfonyl)phenol represented by chemical formula (S2) shown below with 4,4′-dichlorodiphenylsulfone represented by chemical formula (S3) shown below.

##STR00001##

wherein hydrogen atoms in phenylene groups in formula (S1), formula (S2) and formula (S3) may be each independently substituted with an alkyl group, an aryl group or a halogen atom.

POLYMER COMPOSITE MATERIAL COMPRISING ARAMID NANOFIBER, AND METHOD FOR PREPARING SAME

The present invention relates to a polymer composite material comprising an aramid nanofiber (ANF), and a method for preparing same. More specifically, the present invention relates to an arylene ether-based polymer or arylene ether imide-based polymer composite material which is obtained by mixing an arylene ether-based polymer or an arylene ether imide-based polymer with aramid nanofibers dispersed in a polar aprotic solution or by adding and polymerizing monomers in the dispersion of aramid nanofibers.

Fabrication of Luminescent Quantum Dot Thiol-yne Nanocomposites With Tailorable Optical, Thermal and Mechanical Properties

This disclosure concerns a method of making a ligand for Quantum Dot functionalization, a method of making a functionalized Quantum Dot (QD) with a ligand, and a method of making a transparent luminescent quantum dot thiol-yne nanocomposite with tailorable optical, thermal, and mechanical properties. The prepolymer solution and functionalized Quantum Dot can be used in additive manufacturing.

AROMATIC POLYETHERS CONTAINING A BIOSOURCED FURAN DIOL

The present invention relates to a polymer of the aromatic polyether type, containing a biosourced furan diol, to a method for producing said polymer, and to the use of said polymer for producing membranes.

Methods of manufacture of thermoplastic polymers

A method of manufacture of a polyetherimide copolymer composition includes contacting a substituted phthalic anhydride and an organic diamine in the presence of diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing solvents at a temperature of greater than 130° C. to provide a bis(phthalimide) composition comprising diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing solvents and a bis(phthalimide); and copolymerizing the bis(phthalimide), a substituted aromatic compound, and an alkali metal salt of a dihydroxy aromatic compound in the presence of diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing to form a polyetherimide copolymer. The method does not require any catalyst either for the imidization or the polymerization.