C08F4/04

BIO-BASED ETHYLENE FOR THE PRODUCTION OF BIO-BASED POLYMERS, COPOLYMERS, AND OTHER BIO-BASED CHEMICAL COMPOUNDS

Bio-based ethanol, such as ethanol produced from lignocellulosic materials, for example, is processed to produce bio-based ethylene, which can then be processed further to produce other bio-based materials including bio-based polymers and copolymers, including bio-based polyethylene, bio-based α-olefins, bio-based 1,2-diols, as well as other compounds.

BIO-BASED ETHYLENE FOR THE PRODUCTION OF BIO-BASED POLYMERS, COPOLYMERS, AND OTHER BIO-BASED CHEMICAL COMPOUNDS

Bio-based ethanol, such as ethanol produced from lignocellulosic materials, for example, is processed to produce bio-based ethylene, which can then be processed further to produce other bio-based materials including bio-based polymers and copolymers, including bio-based polyethylene, bio-based α-olefins, bio-based 1,2-diols, as well as other compounds.

Ethylene-(Vinyl Alcohol) Copolymer and Method for Producing Same
20220195159 · 2022-06-23 · ·

Provided is an ethylene-vinyl alcohol copolymer with an ethylene unit content of 15 to 60 mol % and a saponification degree of 85 mol % or more.

Ethylene-(Vinyl Alcohol) Copolymer and Method for Producing Same
20220195159 · 2022-06-23 · ·

Provided is an ethylene-vinyl alcohol copolymer with an ethylene unit content of 15 to 60 mol % and a saponification degree of 85 mol % or more.

Fluorine-containing alternating copolymer macromonomer and synthesis method thereof

The present invention relates to a fluorine-containing alternating copolymer macromonomer and a synthesis method thereof. The synthesis method comprises steps of: subjecting a fluorine-containing alternating copolymer to a reduction reaction at 60-100° C. in an organic solvent in the presence of a reducing agent and a first catalyst to obtain a reduction product; in the presence of a second catalyst, reacting the reduction product with a mercapto-monohydric alcohol in an organic solvent at 60-100° C., to obtain a hydroxyl-terminated fluorine-containing alternating copolymer; and in the presence of a third catalyst, reacting the hydroxyl-terminated fluorine-containing alternating copolymer with an acrylic monomer or acryloyl chloride monomer at 0-30° C., to obtain the fluorine-containing alternating copolymer macromonomer. In the present invention, a fluorine-containing alternating copolymer macromonomer is initially synthesized from a fluorine-containing alternating copolymer through polymer modification.

Fluorine-containing alternating copolymer macromonomer and synthesis method thereof

The present invention relates to a fluorine-containing alternating copolymer macromonomer and a synthesis method thereof. The synthesis method comprises steps of: subjecting a fluorine-containing alternating copolymer to a reduction reaction at 60-100° C. in an organic solvent in the presence of a reducing agent and a first catalyst to obtain a reduction product; in the presence of a second catalyst, reacting the reduction product with a mercapto-monohydric alcohol in an organic solvent at 60-100° C., to obtain a hydroxyl-terminated fluorine-containing alternating copolymer; and in the presence of a third catalyst, reacting the hydroxyl-terminated fluorine-containing alternating copolymer with an acrylic monomer or acryloyl chloride monomer at 0-30° C., to obtain the fluorine-containing alternating copolymer macromonomer. In the present invention, a fluorine-containing alternating copolymer macromonomer is initially synthesized from a fluorine-containing alternating copolymer through polymer modification.

AQUEOUS EMULSION AND ADHESIVE USING SAME

An aqueous emulsion may include an ethylene-vinyl alcohol copolymer (A) as a dispersant and a polymer (B) which contains an ethylenically unsaturated monomer unit as a dispersoid, wherein the ethylene-vinyl alcohol copolymer (A) has an ethylene unit content of 1 mol % or more and less than 20 mol %; and a crystallinity in water at 30° C. (Cw (30° C.)) and a crystallinity in water at 70° C. (Cw (70° C.)) as determined by pulse NMR satisfying formula (I). Such aqueous emulsions can form fewer aggregates and exhibit excellent water-resistant adhesiveness and excellent film formability.

CONDUCTIVE MATERIAL DISPERSION, BINDER RESIN-CONTAINING CONDUCTIVE MATERIAL DISPERSION, SLURRY FOR ELECTRODE FILM, ELECTRODE FILM, AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY

A conductive material dispersion containing a conductive material containing carbon fibers, a dispersant, and a dispersion medium, in which the dispersant contains a copolymer A containing a nitrile group-containing structural unit and an aliphatic hydrocarbon structural unit, and a Mooney viscosity (ML.sub.1+4, 100° C.) of the copolymer A is 40 to 70, and the conductive material dispersion has a phase angle of 19° or greater at a frequency of 1 Hz.

CONDUCTIVE MATERIAL DISPERSION, BINDER RESIN-CONTAINING CONDUCTIVE MATERIAL DISPERSION, SLURRY FOR ELECTRODE FILM, ELECTRODE FILM, AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY

A conductive material dispersion containing a conductive material containing carbon fibers, a dispersant, and a dispersion medium, in which the dispersant contains a copolymer A containing a nitrile group-containing structural unit and an aliphatic hydrocarbon structural unit, and a Mooney viscosity (ML.sub.1+4, 100° C.) of the copolymer A is 40 to 70, and the conductive material dispersion has a phase angle of 19° or greater at a frequency of 1 Hz.

CONDUCTIVE MATERIAL DISPERSION, BINDER RESIN-CONTAINING CONDUCTIVE MATERIAL DISPERSION, SLURRY FOR ELECTRODE FILM, ELECTRODE FILM, AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY

A conductive material dispersion containing a conductive material containing carbon fibers, a dispersant, and an amide-based organic solvent, in which the dispersant contains a copolymer A containing a nitrile group-containing structural unit and satisfies following conditions.

(I) A pH of the conductive material dispersion is 9.0 or greater.

(II) A phase angle of the conductive material dispersion at a frequency of 1 Hz obtained by dynamic viscoelasticity measurement is 19° or greater, and a complex elastic modulus of the conductive material dispersion obtained by dynamic viscoelasticity measurement is less than 20 Pa.