IP Library › Granted Patent US 7,714,062
Granted Patent B2
US 7,714,062 · App. 12/002,695 · Granted May 11, 2010

Thermal curable powder coating composition

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Quick Facts
Patent No.
US 7,714,062
App. No.
12/002,695
Granted
May 11, 2010
Kind
B2
Abstract

A powder coating composition comprising (A) at least one hydroxyl functional polyurethane resin binder, and (B) at least one polyurethane resin as cross-linking agent containing blocked isocyanate groups, wherein the at least one hydroxyl functional polyurethane resin binder (A) and the at least one polyurethane resin (B) both having a melting temperature of 60 to 180° C., in particular, 80 to 160° C.; the powder coating composition makes it possible to achieve a low melt viscosity and an excellent processability along with a good storage stability and in particular, to form thin films of the coating layers having high flexibility in combination with an excellent weather resistance.

Claims (17)

1. A powder coating composition comprising

(A) at least one hydroxyl functional polyurethane resin binder, and

(B) at least one polyurethane resin as cross-linking agent containing blocked isocyanate groups, wherein the at least one hydroxyl functional polyurethane resin binder (A) and the at least one polyurethane resin (B) both have a melting temperature of 60° C. to 180° C., wherein the melting temperatures are the upper end of melting ranges with a breadth of 30° C. to 150° C. and wherein the melting temperatures and the melting ranges are determined by differential scanning calorimetry at heating rates of 10 K/mm, and

wherein the polyurethane resin (B) is a polyurethane with two blocked isocyanate groups per molecule which is the reaction product of 1,6-hexane diisocyanate with a diol component and with at least one blocking agent in the molar ratio x mol 1,6-hexane diisocyanate:x−1 mol diol component: 2 mol blocking agent, wherein x means a value from 2 to 6.

2. The composition according claim 1 comprising

(A) 20 to 80 wt % of at least one hydroxyl functional polyurethane resin binder,

(B) 80 to 20 wt % at least one polyurethane resin as cross-linking agent containing blocked isocyanate groups,

(C) 0 to 50 wt % of at least one binder different from (A) and (B), having functional groups reactive with the functional groups of (A) and (B), and

(D) 0.1 to 60 wt % of pigments, fillers and/or coating additives, the wt % amounts based on the total weight of the powder coating composition (A) to (D), wherein the at least one hydroxyl functional polyurethane resin binder (A) and the at least one polyurethane resin (B) both having a melting temperature of 80° C. to 160° C.

3. The composition according to claim 1 wherein the polyurethane resin binder (A) is a polyurethane diol which is the reaction product of 1,6-hexane diisocyanate and a diol component in the molar ratio of x mol 1,6 hexane diisocyanate: (x+1) mol diol component, wherein x means a value from 2 to 6.

4. The composition according to claim 1 wherein the polyurethane resin binder (A) is a polyurethane diol which is the reaction product of a diisocyanate component and a diol component in the molar ratio of x mol diisocyanate component: (x+1) mol diol component, wherein x means a value from 2 to 6, wherein 50 to 80 mol % of the diisocyanate component is formed by 1,6-hexane diisocyanate, and 20 to 50 mol % by one or two diisocyanates, each forming at least 10 mol % of the diisocyanate component and being selected from the group consisting of toluylene diisocyanate, diphenylmethane diisocyanate, dicyclohexylmethane diisocyanate, isophorone diisocyanate, trimethylhexane diisocyanate, cyclohexane diisocyanate, cyclohexanedimethylene diisocyanate and tetramethylenexylylene diisocyanate.

5. The composition according to claim 4 wherein 20-100 mol % of the diol component is formed by at least one linear aliphatic alpha,omega-C2-C12-diol.

6. The composition according to claim 1 wherein the diisocyanate component of polyurethane resin (B) comprises from 50 to 80 mol % of 1,6-hexane diisocyanate and 20 to 50 mol % of one or two diisocyanates, each forming at least 10 mol % of the diisocyanate component and being selected from the group consisting of toluylene diisocyanate, diphenylmethane diisocyanate, dicyclohexylmethane diisocyanate, isophorone diisocyanate, trimethylhexane diisocyanate, cyclohexane diisocyanate, cyclohexanedimethylene diisocyanate and tetramethylenexylylene diisocyanate.

7. A process of coating a substrate comprising the steps

(a) applying the coating composition of claim 1 on a substrate and

(b) curing the applied composition.

8. A substrate coated with the powder coating composition according to claim 1 .

Assignments (6)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2008
From: FLOSBACH, CARMEN; ILAND, KRISTINA; RENKES, TANJA
To: E. I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 020674/0803 →
Continuity (2)
Provisional Application 6087686900 · Dec 22, 2006
Related Publication 20080152900A1 · Jun 26, 2008