IP Library Granted Patent US 7,737,243
Granted Patent B2
US 7,737,243 · App. 11/804,048 · Granted Jun 15, 2010

Highly productive coating composition for automotive refinishing

Assignee: E. I. du Pont de Nemours and Company
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Quick Facts
Patent No.
US 7,737,243
App. No.
11/804,048
Granted
Jun 15, 2010
Kind
B2
Abstract

This invention relates to coating compositions and more particularly to highly productive coating compositions that quickly harden for sanding or buffing by incorporating therein a polyisocyanate adduct mixture into the coating composition as the crosslinking material. Such coatings are particularly useful for refinishing automobiles and trucks.

Claims (27)

1. A urea-containing polyisocyanate adduct mixture consisting essentially of the reaction product of;

a) at least one aliphatic isocyanate trimer; and

b) at least one cycloaliphatic isocyanate trimer in the presence of

c) a urea-forming agent; and

wherein the mole ratio of said aliphatic to cycloaliphatic trimer is in the range of from 1:2 to 1:10 and the reaction product has a molecular weight average of from 500 to 3000 and an isocyanate functionality of at least 4.

2. The composition of claim 1 wherein said aliphatic isocyanate trimer is prepared from hexamethylene diisocyanate.

3. The composition of claim 1 wherein said cycloaliphatic isocyanate trimer is prepared from isophorone diisocyanate.

4. The composition of claim 1 , wherein said reaction is conducted at a temperature of between 50° C. and 180° C.

5. A coating composition comprising

a) a crosslinkable binder;

b) a crosslinking component capable of crosslinking with said crosslinkable binder and;

c) optionally a liquid carrier

wherein said crosslinkable binder has functional groups that are crosslinkable with b) and said crosslinking component comprises the polyisocyanate adduct mixture of claim 1 .

6. The coating composition of claim 5 wherein said aliphatic isocyanate trimer is the isocyanurate of hexamethylene diisocyanate.

7. The coating composition of claim 5 wherein said cycloaliphatic isocyanate trimer is the isocyanurate of isophorone diisocyanate.

8. The coating composition of claim 5 wherein said coating composition is a solvent borne or a waterborne primer.

9. The coating composition of claim 5 wherein said coating composition is a solvent borne or a waterborne primer/surfacer.

10. The coating composition of claim 5 wherein said coating composition is a pigmented solvent borne and/or waterborne basecoat used in a basecoat/clearcoat paint system.

11. The coating composition of claim 5 wherein said coating composition is a solventborne clearcoat in a solvent borne and/or waterborne basecoat/clearcoat paint system.

12. The coating composition of claim 5 wherein said coating composition is a solvent borne or waterborne single stage paint system.

13. The coating composition of claim 5 wherein said coating composition is a waterborne coating composition.

14. The coating composition of claim 5 wherein said coating composition is a solvent borne coating composition.

15. The coating composition of claim 5 wherein said coating composition is a powder coating.

16. The coating composition of claim 5 wherein said coating composition is suitable for the production of the basecoat or clearcoat or undercoat in a clearcoat/color coat finish for automobiles and trucks.

17. A substrate coated with a dried cured layer of the coating composition of claim 5 .

18. An automotive substrate coated with a dried cured multi-layer coating, wherein at least one of the dried cured coating layers is the coating composition of claim 5 .

19. A process for preparing a urea-containing polyisocyanate adduct mixture having a functionality of at least 4 which consists essentially of reacting an aliphatic isocyanate trimer and a cycloaliphatic isocyanate trimer; wherein each of said aliphatic isocyanate trimer and cycloaliphatic isocyanate trimer has an average isocyanate functionality of at least 2.8; and contain at least 50 mole percent of isocyanurate and/or iminooxadiazine dione groups, based on the total moles of isocyanate adduct groups present in said isocyanate trimers, with 0.01 to 0.15 moles of water for each equivalent of isocyanate groups in the isocyanate trimers at a temperature of 50 to 180° C. to incorporate urea-groups into the polyisocyanate adduct mixture, wherein the mole ratio of aliphatic isocyanate trimer to cycloaliphatic isocyanate trimer is in the range of from 1:2 to 1:10.

Assignments (8)
CHANGE OF NAME Recorded Oct 24, 2016
From: BAYER MATERIALSCIENCE AKTIENGESELLSCHAFT (AG)
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 040264/0007 →
CHANGE OF NAME Recorded Oct 24, 2016
From: BAYER MATERIALSCIENCE LLC
To: COVESTRO LLC
Reel/Frame 040264/0120 →
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 Aug 28, 2007
From: ADAMS, JEROME T.; MAGER, DIETER; SHAFFER, MYRON W.; BARSOTTI, ROBERT JOHN; LEWIN, LAURA ANN; ADAMS, JAMES LAMONTE; O'NEIL, JAMES WILLIAM; HALPAAP, REINHARD
To: E. I. DU PONT DE NEMOURS AND COMPANY; BAYER MATERIALSCIENCE LLC; BAYER MATERIALSCIENCE AKTIENGESELLSCHAFT
Reel/Frame 019753/0128 →
Continuity (2)
Provisional Application 6080080700 · May 16, 2006
Related Publication 20070282070A1 · Dec 6, 2007