C08F2/16

Aqueous resin dispersion, production method for aqueous resin dispersion, hydrophilization agent, hydrophilization method, metal material, and heat exchanger

Provided are an aqueous resin dispersion of an ethylene-vinyl alcohol copolymer exhibiting excellent dispersion stability, a production method for the aqueous resin dispersion, a hydrophilization agent including the aqueous resin dispersion, a hydrophilization method using the hydrophilization agent, a metal material on which a hydrophilic coating has been formed, and a heat exchanger on which a hydrophilic coating has been formed. Specifically provided are: an aqueous resin dispersion comprising an ethylene-vinyl alcohol copolymer (A) and a radical polymer (B) having a structural unit derived from a radical-polymerizable carboxylic acid monomer (B1-1), wherein the content of the radical polymer (B) is 10-80 mass % relative to the total content of the ethylene-vinyl alcohol copolymer (A) and the radical polymer (B); a production method for the aqueous resin dispersion; a hydrophilization agent including the aqueous resin dispersion; a hydrophilization method using the hydrophilization agent; a metal material on which a hydrophilic coating has been formed; and a heat exchanger on which a hydrophilic coating has been formed.

COPOLYMER

Provided is a copolymer consisting essentially of ethylene units, tetrafluoroethylene units, and hexafluoropropylene units, wherein a molar ratio (Et units/TFE units) of the ethylene (Et) units to the tetrafluoroethylene (TFE) units is 52.0/48.0 to 56.0/44.0, and a content of the hexafluoropropylene units is 19.0 to 21.0 mol % based on the total monomer units constituting the copolymer.

COPOLYMER

Provided is a copolymer consisting essentially of ethylene units, tetrafluoroethylene units, and hexafluoropropylene units, wherein a molar ratio (Et units/TFE units) of the ethylene (Et) units to the tetrafluoroethylene (TFE) units is 52.0/48.0 to 56.0/44.0, and a content of the hexafluoropropylene units is 19.0 to 21.0 mol % based on the total monomer units constituting the copolymer.

Method for the synthesis of fluoropolymers

The present invention relates to a fluorosurfactant-free emulsion polymerization method for the synthesis of a fluoropolymer, more in particular of a VDF-based polymer.

Method for the synthesis of fluoropolymers

The present invention relates to a fluorosurfactant-free emulsion polymerization method for the synthesis of a fluoropolymer, more in particular of a VDF-based polymer.

ENZYME-ASSISTED ATRP PROCEDURES

Materials and methods for conducting an atom transfer radical polymerization in the presence of oxygen by interlocking enzymatic activities are provided herein.

ENZYME-ASSISTED ATRP PROCEDURES

Materials and methods for conducting an atom transfer radical polymerization in the presence of oxygen by interlocking enzymatic activities are provided herein.

Enzyme-assisted ATRP procedures

Materials and methods for conducting an atom transfer radical polymerization in the presence of oxygen by interlocking enzymatic activities are provided herein.

Enzyme-assisted ATRP procedures

Materials and methods for conducting an atom transfer radical polymerization in the presence of oxygen by interlocking enzymatic activities are provided herein.

Aqueous polymerization of perfluoromonomer using hydrocarbon surfactant

A process is provided for the polymerization of fluoromonomer to an dispersion of fluoropolymer particles in an aqueous medium in a polymerization reactor, by (a) providing the aqueous medium in the reactor, (b) adding the fluoromonomer to the reactor, (c) adding initiator to the aqueous medium, the combination of steps (b) and (c) being carried out essentially free of hydrocarbon-containing surfactant and resulting in the kickoff of the polymerization of the fluoromonomer, and (d) metering hydrocarbon-containing surfactant into the aqueous medium after the kickoff of polymerization, e.g. after the concentration of the fluoropolymer in the aqueous medium is at least 0.6 wt %, the metering being at a rate reducing the telogenic activity of said surfactant while maintaining surface activity.