IP Library Granted Patent US 8,865,843
Granted Patent B2
US 8,865,843 · App. 13/496,224 · Granted Oct 21, 2014

Fluorinated sag control agent and use thereof

Inventors: Rajesh Gopalan Saliya (Philadelphia, PA); Ayumu Yokoyama (Wallingford, PA); Sheau-Hwa Ma (West Chester, PA); Axel Hans-Joachim Herzog (West Chester, PA)
Assignee: Axalta Coating Systems IP Co., LLC
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Quick Facts
Patent No.
US 8,865,843
App. No.
13/496,224
Granted
Oct 21, 2014
Kind
B2
Abstract

The present disclosure is directed to a sag control agent comprising a reaction product of an isocyanate and a fluorinated amine. This disclosure is further directed to a coating composition comprising the sag control agent. This disclosure is also directed to a process of forming a sag-free coating layer on a substrate.

Claims (31)

1. A sag control agent comprising a reaction product of reactants comprising an isocyanate component comprising an isocyanate and an amine component comprising a fluorinated amine, wherein said fluorinated amine has the formula:

Rf—X—NH 2   (I)

wherein, Rf is a fluorocarbon or perfluorocarbon having 1 to 20 carbon atoms, and X is a connecting di radical C 6 to C 20 aryl, O—R 1 —S(O) k —R 1′ , R 1 —S(O) k —R 1′ , R 1 —NR 2 —R 1′ , C 1 to C 20 substituted alkyl wherein one or more hydrogen atoms are substituted with a C 1 to C 10 alkyl or C 1 to C 10 substituted alkyl, C 6 to C 20 substituted aryl wherein one or more hydrogen atoms are substituted with a C 1 to C 10 alkyl or C 1 to C 10 substituted alkyl, or a combination thereof, k=0, 1 or 2; wherein R 1 or R 1′ is independently C 1 to C 10 alkyl, C 6 to C 10 aryl, C 1 to C 10 substituted alkyl, C 6 to C 10 substituted aryl, or a combination thereof, and wherein R 2 is H, C 1 to C 10 alkyl, C 6 to C 10 aryl, C 1 to C 10 substituted alkyl, or C 6 to C 10 substituted aryl.

2. The sag control agent of claim 1 further comprising a pigment.

3. The sag control agent of claim 1 , wherein X is a connecting di-radical O(CH 2 ) m —S(O) k —(CH 2 ) n , (CH 2 ) m —S(O) k —(CH 2 ) n , (CH 2 ) m —NR 2 —(CH 2 ) n , substituted (CH 2 ) m wherein one or more hydrogen atoms are substituted with a C 1 to C 10 alkyl or C 1 to C 10 substituted alkyl, O(CH 2 ) m —S(O) k —(CH 2 ) n , (CH 2 ) m —S(O) k —(CH 2 ) n , or (CH 2 ) m —NR 2 —(CH 2 ) n , wherein m and n are independently zero or positive integers, and m+n is in a range of from 3 to 20.

4. The sag control agent of claim 3 , wherein m+n is in a range of from 3 to 6.

5. The sag control agent of claim 1 , wherein said fluorocarbon or said perfluorocarbon has 1 to 8 carbon atoms.

6. The sag control agent of claim 1 , wherein said amine component comprises one or more fluorinated amines selected from the group consisting of C 6 F 13 C 2 H 4 —S—C 2 H 4 NH 2 , C 6 F 13 C 2 H 4 —S(O)—C 2 H 4 NH 2 , C 6 F 13 C 2 H 4 —S(O) 2 —C 2 H 4 NH 2 , CF 3 (CF 2 ) 2 O(CF 2 ) 2 C 2 H 4 —S—C 2 H 4 NH 2 , and a combination thereof.

7. The sag control agent of claim 1 , wherein said isocyanate is a monoisocyanate, a diisocyanate, a trimer of diisocyanate, a polyisocyanate, or a combination thereof.

8. The sag control agent of claim 1 , wherein said isocyanate is hexamethylene diisocyanate.

9. The sag control agent of claim 1 further comprising one or more polymers.

10. The sag control agent of claim 9 , wherein said one or more polymers are one or more acrylic polymers, one or more polyester polymers, one or more polyether polymers, or a combination thereof.

11. The sag control agent of claim 10 , wherein said one or more acrylic polymers comprise a hydroxyl acrylic polymer.

12. The sag control agent of claim 10 , wherein said one or more polyether polymers comprise a polytrimethylene ether diol having a Mn (number average molecular weight) in a range of from 500 to 10,000.

13. The sag control agent of claim 12 , wherein said polytrimethylene ether diol is polymerized from bio-derived 1,3-propanediol.

14. The sag control agent of claim 1 further comprising one or more solvents.

15. The sag control agent of claim 1 , wherein said sag control agent comprises a reaction product of reactants consisting of said isocyanate component and said amine component.

16. The sag control agent of claim 1 , wherein said sag control agent comprises a reaction product of reactants consisting of hexamethylene diisocyanate and one or more fluorinated amines selected from the group consisting of C 6 F 13 C 2 H 4 —S—C 2 H 4 NH 2 , C 6 F 13 C 2 H 4 —S(O)—C 2 H 4 NH 2 , C 6 F 13 C 2 H 4 —S(O) 2 —C 2 H 4 NH 2 , CF 3 (CF 2 ) 2 O(CF 2 ) 2 C 2 H 4 —S—C 2 H 4 NH 2 , and a combination thereof.

17. The sag control agent of claim 1 , wherein said amine component further comprises a non-fluorinated primary amine, a non-fluorinated secondary amine, or a combination thereof.

18. The sag control agent of claim 1 , wherein said amine component comprises 50% to 100%, weight percent of the total weight of the amine component, of said fluorinated amine.

19. The sag control agent of claim 1 further comprising a polymer binder of a coating composition, wherein the polymer binder comprises a crosslinkable component and a crosslinking component.

20. A process for forming a sag-free coating layer on a substrate, said process comprising the steps of:

A) applying a coating composition over said substrate forming a sag-free wet coating layer having a wet coating thickness in a range of from 8 to 36 mils, wherein said coating composition comprises:

i) a sag control agent comprising a reaction product of reactants comprising an isocyanate component comprising an isocyanate and an amine component comprising a fluorinated amine having the formula:

Rf—X—NH 2   (I)

wherein, Rf is a fluorocarbon or perfluorocarbon having 1 to 20 carbon atoms, and X is a connecting di-radical, C 6 to C 20 aryl, O—R 1 —S(O) k —R 1′ , R 1 —S(O) k —R 1′ , R 1 —NR 2 —R 1′ , C 1 to C 20 substituted alkyl wherein one or more hydrogen atoms are substituted with a C 1 to C 10 alkyl or C 1 to C 10 substituted alkyl, C 6 to C 20 substituted aryl wherein one or more hydrogen atoms are substituted with a C 1 to C 10 alkyl or C 1 to C 10 substituted alkyl, or a combination thereof, k=0, 1 or 2; wherein R 1 or R 1′ is independently C 1 to C 10 alkyl, C 6 to C 10 aryl, C 1 to C 10 substituted alkyl, C 6 to C 10 substituted aryl, or a combination thereof, and wherein R 2 is H, C 1 to C 10 alkyl, C 6 to C 10 aryl, C 1 to C 10 substituted alkyl, or C 6 to C 10 substituted aryl; and

ii) a polymer binder; and

B) curing said sag-free wet coating layer to form said sag-free coating layer.

21. The process of claim 20 , wherein said step B) is performed at a temperature in a range of from 15° C. to 50° C.

22. The process of claim 20 , wherein said sag-free wet coating layer has a wet coating thickness in a range of from 10 to 36 mils.

23. The process of claim 20 , wherein said sag-free coating layer has a dry coating thickness in a range of from 4 to 20 mils.

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 →
Continuity (2)
Provisional Application 61246163 · Sep 28, 2009
Related Publication 20120171478A1 · Jul 5, 2012