IP Library Granted Patent US 10,781,283
Granted Patent B2
US 10,781,283 · App. 15/569,130 · Granted Sep 22, 2020

Crosslinkable fluorinated urethane additives for durable exterior coatings

Inventors: Anilkumar Raghavanpillai (Wilmington, DE); Michael Henry Ober (Newark, DE); Vincent Franco (Wilmington, DE)
Assignee: THE CHEMOURS COMPANY FC, LLC
C08G18/3802C08G18/0823C08G18/222C08G18/246C08G18/2825C08G18/2885C08G18/348C08G18/3825C08G18/3831C08G18/3848C08G18/3851C08G18/672C08G18/6715C08K5/0025C09D5/1687C09D7/65C09D175/16C08G2261/76C08K5/205C08K5/21C08K5/34924
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Quick Facts
Patent No.
US 10,781,283
App. No.
15/569,130
Granted
Sep 22, 2020
Kind
B2
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.

Claims (20)

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.

Assignments (3)
SECURITY INTEREST Recorded Apr 4, 2018
From: THE CHEMOURS COMPANY FC, LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 045846/0011 →
MERGER AND CHANGE OF NAME Recorded Mar 11, 2018
From: THE CHEMOURS COMPANY TT, LLC; THE CHEMOURS COMPANY FC, LLC
To: THE CHEMOURS COMPANY FC, LLC
Reel/Frame 045170/0559 →
MERGER AND CHANGE OF NAME Recorded Nov 16, 2017
From: THE CHEMOURS COMPANY TT, LLC; THE CHEMOURS COMPANY FC, LLC
To: THE CHEMOURS COMPANY FC, LLC
Reel/Frame 044774/0297 →