C08F216/08

SECONDARY BATTERY, METHOD FOR PREPARING THE SAME, COPOLYMER AND APPARATUS

The present application discloses a secondary battery, a method for preparing the same, a copolymer and an apparatus. The secondary battery includes a binder for binding a first substance and a second substance, the binder including a copolymer, wherein the copolymer comprises at least a first monomer unit represented by formula (I), a second monomer unit represented by formula (II), and a third monomer unit represented by formula (III):

##STR00001##

The secondary battery provided by the present application can effectively increase the boding force between the first substance and the second substance by including a specific binder, thereby improving the electrochemical performance of the secondary battery.

Olefin-acrylate copolymers with pendant hydroxyl functionality and use thereof

Copolymers prepared by a reaction of (1) an unactivated olefin, (2) an activated olefin, and (3) a hydroxyl functional activated olefin and/or a hydroxyl functional unactivated olefin are described. The copolymers have a backbone of polar vinyl monomers and non-polar alkene monomers, with pendant hydroxyl functional groups. The copolymers are well suited for optically clear, pressure sensitive, polyurethane and/or barrier adhesives.

Olefin-acrylate copolymers with pendant hydroxyl functionality and use thereof

Copolymers prepared by a reaction of (1) an unactivated olefin, (2) an activated olefin, and (3) a hydroxyl functional activated olefin and/or a hydroxyl functional unactivated olefin are described. The copolymers have a backbone of polar vinyl monomers and non-polar alkene monomers, with pendant hydroxyl functional groups. The copolymers are well suited for optically clear, pressure sensitive, polyurethane and/or barrier adhesives.

Polymers and uses thereof

The present invention provides polymers and methods of preparing the same. In certain embodiments, the polymers comprise acrylate repeating units that have been derivatized (e.g., reduced and/or substituted) to form new polymeric structures. In certain embodiments, the polymers described herein self-assemble to form well-defined nanostructures. In some instances, the nanostructures exhibit relatively small d-spacing (e.g., a d-spacing value of 10 nm or less). Due to their properties, the polymers described herein are useful in a variety of applications including functional materials and biomedical applications.

GAS-BARRIER RESIN COMPOSITION AND USE THEREOF

A gas-barrier resin (A) having an oxygen permeability coefficient of 1.0×10.sup.−14 (cm.sup.3.Math.cm/cm.sup.2.Math.s.Math.Pa) or less; and a copolymer (B) containing monomer structural units represented by the formula (1), the formula (2), and the formula (3):

##STR00001##

where: R.sup.1 represents a hydrogen atom or a methyl group; R.sup.2 represents a hydrocarbon group having 1 to 20 carbon atoms that may be substituted with a halogen atom, a hydroxy group, an alkoxy group, or an amino group; 1, m, and n represent numerical values representing molar proportions of the respective monomer structural units, and n may represent 0; and p represents an integer of from 1 to 4, wherein a ratio of a mass of the copolymer (B) to a total mass of the gas-barrier resin (A) and the copolymer (B) is from 1 mass % to 40 mass %.

GAS-BARRIER RESIN COMPOSITION AND USE THEREOF

A gas-barrier resin (A) having an oxygen permeability coefficient of 1.0×10.sup.−14 (cm.sup.3.Math.cm/cm.sup.2.Math.s.Math.Pa) or less; and a copolymer (B) containing monomer structural units represented by the formula (1), the formula (2), and the formula (3):

##STR00001##

where: R.sup.1 represents a hydrogen atom or a methyl group; R.sup.2 represents a hydrocarbon group having 1 to 20 carbon atoms that may be substituted with a halogen atom, a hydroxy group, an alkoxy group, or an amino group; 1, m, and n represent numerical values representing molar proportions of the respective monomer structural units, and n may represent 0; and p represents an integer of from 1 to 4, wherein a ratio of a mass of the copolymer (B) to a total mass of the gas-barrier resin (A) and the copolymer (B) is from 1 mass % to 40 mass %.

ETHYLENE-VINYL ALCOHOL COPOLYMER, METHOD FOR PRODUCING SAME, AND USE THEREOF

There is provided an ethylene-vinyl alcohol copolymer with an ethylene unit content of 1 mol % or more and less than 20 mol %, a viscosity-average polymerization degree of 200 to 5000 and a saponification degree of 80 to 99.7 mol %, wherein a block character of ethylene units in the ethylene-vinyl alcohol copolymer is 0.90 to 0.99. Such an ethylene-vinyl alcohol copolymer has excellent high-speed coating ability and water-resistant adhesiveness, particularly when being used as an adhesive.

ETHYLENE-VINYL ALCOHOL COPOLYMER, METHOD FOR PRODUCING SAME, AND USE THEREOF

There is provided an ethylene-vinyl alcohol copolymer with an ethylene unit content of 1 mol % or more and less than 20 mol %, a viscosity-average polymerization degree of 200 to 5000 and a saponification degree of 80 to 99.7 mol %, wherein a block character of ethylene units in the ethylene-vinyl alcohol copolymer is 0.90 to 0.99. Such an ethylene-vinyl alcohol copolymer has excellent high-speed coating ability and water-resistant adhesiveness, particularly when being used as an adhesive.

WATER-ABSORBENT RESIN AND AGRICULTURAL WATER-RETAINING MATERIAL
20200347164 · 2020-11-05 · ·

A water-absorbent resin containing a vinyl alcohol-based polymer and having a crystal melting enthalpy of more than 0 J/g in a dry state.

WATER-ABSORBENT RESIN AND AGRICULTURAL WATER-RETAINING MATERIAL
20200347164 · 2020-11-05 · ·

A water-absorbent resin containing a vinyl alcohol-based polymer and having a crystal melting enthalpy of more than 0 J/g in a dry state.