IP Library Granted Patent US 8,293,321
Granted Patent B2
US 8,293,321 · App. 12/983,939 · Granted Oct 23, 2012

Coating compositions having improved early hardness

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Quick Facts
Patent No.
US 8,293,321
App. No.
12/983,939
Filed
Jan 4, 2011
Granted
Oct 23, 2012
Kind
B2
Art Unit
1762
USPC
525/124
Abstract

A fast hardening clear coating composition for repairing a clear coat/color coat finish or a pigmented mono-coat of a vehicle comprising a film forming binder and an organic liquid carrier, where the binder contains a hydroxyl polymer component comprising (A) hydroxyl-containing acrylic polymer, (B) at least one hydroxyl-terminated component selected from the group consisting of (1) an organic diol having the formula where R 1 and R 2 are individually selected from the group of hydrogen and an alkyl group having 1, 3-5 carbon atoms and (2) a hydroxyl terminated reaction product of trimethylol propane and a lactone; (C) an organic polyisocyanate crosslinking component, at least portion of which comprises a trimer of isophorone diisocyanate or hexamethylene diisocyanate and the composition further contains, a curing catalyst, of a dialkyl tin aliphatic carboxylate, a tertiary aliphatic mono or diamine, an aliphatic carboxylic acid, and optionally, a zinc or calcium organic acid salt in an effective amount such that the coating composition on curing at ambient temperatures is in a water spot free and sufficiently hard state for sanding or buffing within about 2 hours after application or on cool down when baked under normal conditions.

Claims (32)

1. A process for repairing a clear coat of a clear coat/color coat coating composition which comprises applying a layer of a clear coating composition to the clear coat and curing the layer of the applied clear coating composition,

wherein, said clear coating composition contains a film forming binder and a volatile organic liquid carrier for the binder, wherein the film forming binder contains:

(A) a hydroxyl polymer component comprising at least one hydroxyl-containing acrylic polymer;

(B) at least one hydroxyl-terminated component selected from the group consisting of (1) an organic diol having the formula

where R 1 and R 2 are individually selected from the group consisting of hydrogen and an alkyl group having 1, 3-5 carbon atoms and (2) a hydroxyl terminated reaction product of trimethylol propane and a lactone; and

(C) an organic polyisocyanate component, at least a portion of which comprises a trimer selected from the group consisting of a trimer of isophorone diisocyanate and a trimer of hexamethylene diisocyanate and any mixtures thereof, wherein the organic polyisocyanate component further comprises at least one of an asymmetric hexamethylene diisocyanate trimer, a biuret of hexamethylene diisocyanate, a biuret of isophorone diisocyanate and any mixtures thereof;

wherein the ratio of equivalents of isocyanate per equivalent of hydroxyl groups in the binder is in the range of about 0.7/1 to 2.0/1; and

wherein the clear coating composition further contains

(D) a catalyst system for the binder comprising

(i) at least one organotin compound,

(ii) at least one tertiary amine,

(iii) at least one organic carboxylic acid; and

(iv) optionally, at least one organic acid salt selected from the group consisting of zinc organic acid salts and calcium organic salts;

wherein the clear coating composition cures at ambient temperatures to a water spot free state within 2 hours after application;

wherein the hydroxyl containing acrylic polymer comprises 5 to 50% by weight, based on the weight of the acrylic polymer, of a hydroxyl acrylic polymer having a weight average molecular weight of above 10,000 to 20,000, 20-60% by weight, based on the weight of the acrylic polymer, of a hydroxyl acrylic polymer having a weight average molecular weight of above 7,000 and up to 10,000 and 20-70% by weight by weight, based on the weight of the acrylic polymer, of a hydroxyl acrylic polymer having a weight average molecular weight of 2,000 up to 7,000.

2. A process for repairing a pigmented mono-coat finish which comprises applying a layer of a pigmented coating composition to the mono coat finish and curing the layer of the applied pigmented coating composition,

wherein, said pigmented coating composition contains a film forming binder, one or more pigments and a volatile organic liquid carrier for the binder, wherein the film forming binder contains:

(A) a hydroxyl polymer component comprising at least one hydroxyl-containing acrylic polymer;

(B) at least one hydroxyl-terminated component selected from the group consisting of (1) an organic diol having the formula

where R 1 and R 2 are individually selected from the group consisting of hydrogen and an alkyl group having 1, 3-5 carbon atoms and (2) a hydroxyl terminated reaction product of trimethylol propane and a lactone; and

(C) an organic polyisocyanate component, at least a portion of which comprises a trimer selected from the group consisting of a trimer of isophorone diisocyanate and a trimer of hexamethylene diisocyanate and any mixtures thereof, wherein the organic polyisocyanate component further comprises at least one of an asymmetric hexamethylene diisocyanate trimer, a biuret of hexamethylene diisocyanate, a biuret of isophorone diisocyanate and any mixtures thereof;

wherein the ratio of equivalents of isocyanate per equivalent of hydroxyl groups in the binder is in the range of about 0.7/1 to 2.0/1;

and

wherein the pigmented coating composition further contains

(D) a catalyst system for the binder comprising

(i) at least one organotin compound,

(ii) at least one tertiary amine,

(iii) at least one organic carboxylic acid; and

(iv) optionally, at least one organic acid salt selected from the group consisting of zinc organic acid salts and calcium organic salts;

wherein the one or more pigments are present in the pigmented coating composition in a pigment to binder weight ratio in a range of from about 0.1:100 to 300:100;

wherein the pigmented coating composition cures at ambient temperatures to a water spot free state within 2 hours after application;

wherein the hydroxyl containing acrylic polymer comprises 5 to 50% by weight, based on the weight of the acrylic polymer, of a hydroxyl acrylic polymer having a weight average molecular weight of above 10,000 to 20,000, 20-60% by weight, based on the weight of the acrylic polymer, of a hydroxyl acrylic polymer having a weight average molecular weight of above 7,000 and up to 10,000 and 20-70% by weight by weight, based on the weight of the acrylic polymer, of a hydroxyl acrylic polymer having a weight average molecular weight of 2,000 up to 7,000.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Sep 29, 2016
From: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: AXALTA COATING SYSTEMS IP CO. LLC (FORMERLY KNOWN AS U.S. COATINGS IP CO. LLC)
Reel/Frame 040184/0192 →
SECURITY AGREEMENT Recorded Nov 19, 2013
From: U.S. COATINGS IP CO. LLC (N/K/A AXALTA COATING SYSTEMS IP CO. LLC)
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 031668/0001 →
CHANGE OF NAME Recorded Jun 18, 2013
From: U.S. COATINGS IP CO., LLC
To: AXALTA COATING SYSTEMS IP CO., LLC
Reel/Frame 030639/0164 →
SECURITY AGREEMENT Recorded Mar 28, 2013
From: U.S. COATINGS IP CO. LLC
To: BARCLAYS BANK PLC, AS COLLATERAL AGENT
Reel/Frame 030119/0163 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2013
From: E. I. DU PONT DE NEMOURS AND COMPANY
To: U.S. COATINGS IP CO. LLC
Reel/Frame 029803/0826 →