Crosslinkable fluorinated urethane additives for durable exterior coatings

Patent metadata

Field	Value
Publication number	US-10781283-B2
Application number	US-201615569130-A
Country	US
Kind code	B2
Filing date	Apr 28, 2016
Priority date	Apr 30, 2015
Publication date	Sep 22, 2020
Grant date	Sep 22, 2020

Abstract

The invention relates to a crosslinkable fluorinated urethane compound having at least one ethylenically unsaturated functional group. Such compounds are useful as coatings additives such that, when the coating is applied to a substrate, the additive compound is allowed to first migrate to the surface and subsequently crosslink to form a durable oil-, dirt-, and water-repellent surface.

First claim

What is claimed is:

1. A composition comprising
(i) a coating base selected from a water-dispersed coating, an epoxy polymer coating, an alkyd coating, a Type I urethane coating, or an unsaturated polyester coating; and
(ii) a crosslinkable additive, where the crosslinkable additive is a crosslinkable compound having at least one ethylenically unsaturated functional group comprising the reaction product of reagents comprising:
(a) at least one isocyanate compound having at least 2 isocyanate groups, or a mixture of said compounds;
(b) at least one perfluoroalkyl mono-alcohol of Formula (I), or a mixture of said fluorinated mono-alcohols;
R f -Q v -OH  (I)

wherein
R f is a straight or branched-chain perfluoroalkyl group of 2 to 20 carbon atoms, optionally interrupted by one or more ether oxygens —O—, CH 2 , CFH, or combinations thereof;
Q is a straight chain, branched chain or cyclic structure of alkylene, arylene, aralkylene, sulfonyl, sulfoxy, sulfonamido, carbonamido, carbonyloxy, urethanylene, ureylene, or combinations of such linking groups; and
v is 0 or 1;
(c) at least one isocyanate-reactive compound having one isocyanate-reactive functional group selected from OH, NH 2 , or SH, and having at least one ethylenically unsaturated group;
(d) at least one isocyanate-reactive compound having at least one terminal carboxylic acid and one isocyanate-reactive functional group selected from OH, NH 2 , or SH; and
(e) optionally, at least one additional isocyanate-reactive compound selected from water, alkoxylated diols, or hydroxyl-functional photoinitiator compounds;
provided that if the isocyanate compound (a) has 2 isocyanate groups, then water is present as an additional isocyanate-reactive compound (e);
wherein the composition comprises (i) in an amount of from about 95 to 99.98% and (ii) in an amount of from about 0.02 to 5% by weight, based on the total weight of (i) and (ii).

2. The composition of claim 1 , where R f is a C 1 to C 6 perfluoroalkyl group; v is 1, and Q is a C 1 to C 6 alkylene group.

3. The composition of claim 1 , where the at least one isocyanate-reactive compound (c) is selected from hydroxyalkyl vinyl compounds, straight or branched alcohol containing an alkyl chain of 2 to 30 carbons and having 1 to 15 olefinic units, allylic or methallylic polyether alcohols, aminoalkyl vinyl compounds, acrylic or methacrylic alkyl alcohols, (meth)acrylic polyether alcohols, or (meth)acrylic amines.

4. The composition of claim 1 , where the at least one isocyanate-reactive compound (d) is selected from hydroxyacetic acid, hydroxypropionic acid, or polylactic acid.

5. The composition of claim 1 , where the coating base is a water-dispersed coating selected from an aqueous acrylic latex paint.

6. The composition of claim 1 , where the coating base comprises an additive selected from TiO 2 , clays, asbestos, calcium carbonate, zinc oxide, chromium oxide, barium sulfate, iron oxide, tin oxide, calcium sulfate, talc, mica, silicas, dolomite, zinc sulfide, antimony oxide, zirconium dioxide, silicon dioxide, cadmium sulfide, cadmium selenide, lead chromate, zinc chromate, nickel titanate, diatomaceous earth, glass fibers, glass powders, glass spheres, blue pigments, red pigments, yellow pigments, orange pigments, process aggregated crystals, brown pigments, or green pigments.

Assignees

• Chemours Co Tt Llc
• Chemours Co Fc Llc

Inventors

• Raghavanpillai Anilkumar
• Ober Michael Henry
• Franco Vincent

Classifications

• C09D5/1687

  Use of special additives · CPC title

• C08G18/2885

  containing halogen atoms · CPC title

• C08K5/34924

  containing cyanurate groups; Tautomers thereof · CPC title

• C08K5/0025

  Crosslinking or vulcanising agents; including accelerators · CPC title

• C08G18/0823 Primary

  containing carboxylate salt groups or groups forming them · CPC title