C08L91/005

Thermoplastic elastomers via reversible addition-fragmentation chain transfer polymerization of triglycerides

The present invention relates to a thermoplastic block copolymer comprising at least one PA block and at least one PB block. The PA block represents a polymer block comprising one or more units of monomer A, and the PB block represents a polymer block comprising one or more units of monomer B. Monomer A is a vinyl, acrylic, diolefin, nitrile, dinitrile, acrylonitrile monomer, a monomer with reactive functionality, or a crosslinking monomer. Monomer B is a radically polymerizable triglyceride or mixtures thereof, typically in the form of a plant or animal oil. The present invention also relates to a method of preparing a thermoplastic block copolymer or novel thermoplastic statistical copolymers by polymerizing a radically polymerizable monomer with a radically polymerizable triglyceride or mixtures thereof via reversible addition-fragmentation chain-transfer polymerization (RAFT), in the presence of an free radical initiator and a chain transfer agent.

OXYGEN SCAVENGER

An oxygen scavenger including synthetic amorphous silica impregnated with a drying oil and an oil-soluble metal catalyst.

OXYGEN SCAVENGER

An oxygen scavenger including synthetic amorphous silica impregnated with a drying oil and an oil-soluble metal catalyst.

Solvent borne coating composition having improved sag resistance and process for producing coatings therefrom

A solvent borne brushable coating composition having improved sag resistance and process for using the same are provided. The composition includes a crosslinkable component having one or more polymers having two or more crosslinkable groups a crosslinking component comprising one or more crosslinking agents having crosslinking groups; and a sag control agent of polyurea in drying oil. When a layer a pot mix resulting from mixing of the crosslinkable and crosslinking components is brush applied over a substrate, it has high sag resistance, low brush drag while providing desired coating properties, such as high gloss and rapid cure even under ambient conditions. The solvent borne brushable coating compositions is well suited for use in automotive refinish applications as well as direct-to-metal industrial applications, such as construction and transportation equipment.

Solvent borne coating composition having improved sag resistance and process for producing coatings therefrom

A solvent borne brushable coating composition having improved sag resistance and process for using the same are provided. The composition includes a crosslinkable component having one or more polymers having two or more crosslinkable groups a crosslinking component comprising one or more crosslinking agents having crosslinking groups; and a sag control agent of polyurea in drying oil. When a layer a pot mix resulting from mixing of the crosslinkable and crosslinking components is brush applied over a substrate, it has high sag resistance, low brush drag while providing desired coating properties, such as high gloss and rapid cure even under ambient conditions. The solvent borne brushable coating compositions is well suited for use in automotive refinish applications as well as direct-to-metal industrial applications, such as construction and transportation equipment.

Wood coating compositions

The present invention relates to an improved wood coating composition wherein said composition (C) comprises, relative to the total weight of composition (C), from 58.00 to 95.00 weight percentage of at least one alkyd resin or at least one drying oil, from 0.10 to 8.00 wt. % of at least one microcrystalline wax having a congealing point from 60 C. to 100 C., and from 5.00 to 34.00 wt. % of at least one synthetic micronized wax, said at least one synthetic micronized wax having a particle size D.sub.90 equal to or less than 36.0 m and a particle size D.sub.50 equal to or less than 20.0 m, wherein the congealing point of the microcrystalline wax (W.sub.c) is measured according to the standard ASTM D938, and wherein the particle size of the at least one micronized wax (M.sub.p) is measured according to the standard DIN ISO 13320.