IP Library Patent Application 12937429
Patent Application
App. No. 12/937,429

COATING COMPOSITION CONTAINING POLYTRIMETHYLENE ETHER DIOL

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Patent No.
US None
App. No.
12/937,429
Abstract

The present disclosure is directed to a coating composition having excellent adhesion to primer layers, fast drying, improved flexibility and good pot life. This disclosure is further directed to a coating composition comprising components derived from renewable resources, low Tg acrylic polymers having one or more crosslinkable functional groups and a crosslinking agent having one or more crosslinking functional groups.

Claims (34)

1 . A coating composition comprising a film forming binder, said binder consisting essentially of:

A) an acrylic polymer having one or more crosslinkable functional groups and having a glass transition temperature (Tg) in a range of from −40° C. to 5° C.;

B) a polytrimethylene ether diol having a Mn (number average molecular weight) in a range of from 500 to 10,000; and

C) a crosslinking component containing at least one crosslinking agent having one or more crosslinking functional groups.

2 . The coating composition of claim 1 , wherein the polytrimethylene ether diol has a Mn in a range of from 500 to 4,000, a Tg of about −75° C. and a hydroxyl number in a range of from 20 to 200.

3 . The coating composition of claim 1 , wherein the polytrimethylene ether diol is a blend of high and low molecular weight polytrimethylene ether diols wherein the high molecular weight polytrimethylene ether diol has an Mn in a range of from 1,000 to 4,000 and the low molecular weight polytrimethylene ether diol has an Mn in a range of from 150 to 500 and the average Mn of the blend is in a range of from 1,000 to 4,000.

4 . The coating composition of claim 1 , wherein the polytrimethylene ether diol is polymerized from bio-derived 1,3-propanediol.

5 . The coating composition of claim 1 , wherein at least one of said one or more crosslinkable functional groups is hydroxyl group, and wherein at least one of said one or more crosslinking functional groups is isocyanate group.

6 . The coating composition of claim 1 , wherein the binder consists essentially of:

(a) in a range of from 10% to 80% by weight, based on the weight of the binder, of the acrylic polymer;

(b) in a range of from 1% to 50% by weight, based on the weight of the binder, of the polytrimethylene ether diol; and

(c) in a range of from 10% to 50% by weight, based on the weight of the binder, of the crosslinking component; and

wherein the sum of the percentages of (a), (b) and (c) is 100%.

7 . The coating composition of claim 1 , wherein the acrylic polymer has a weight average molecular weight of 1,000 to 100,000 and a Tg of −40° C. to 5° C. and is polymerized from monomers consisting of:

i) non-functional monomers selected from the group consisting of linear alkyl(meth)acrylates having 1-12 carbon atoms in the alkyl group, cyclic or branched alkyl(meth)acrylates having 3 to 12 carbon atoms in the alkyl group, isobornyl (meth)acrylate, alpha methyl styrene, (meth)acrylonitrile, (meth)acryl amides, and a combination thereof; and

ii) functional monomers selected from the group consisting of hydroxy alkyl(meth)acrylates having 1 to 4 carbon atoms in the alkyl group, glycidyl(meth)acrylates, hydroxy amino alkyl(meth)acrylates having 1 to 4 carbon atoms in the alkyl group, alkoxy silyl alkyl(meth)acrylate and (meth)acrylic acid, and a combination thereof.

8 . The coating composition of claim 1 , wherein the acrylic polymer is polymerized from monomers selected from the group consisting of: styrene, n-butyl acrylate, ethyl methacrylate, methyl methacrylate, butyl acrylate, 2-ethylhexyl acrylate, ethyl acrylate, isobutyl acrylate, 2-ethylhexyl methacrylate, 2-hydroxyethyl acrylate, hydroxypropyl acylate, and a combination thereof.

9 . The coating composition of claim 1 , wherein the acrylic polymer is polymerized from monomers selected from the group consisting of styrene, ethylhexyl methacrylate, n-butyl acrylate, ethyl methacrylate, methyl methacrylate and hydroxyethyl methacrylate.

10 . The coating composition of claim 1 , wherein the crosslinking agent is selected from the group consisting of aliphatic polyisocyanates, cycloaliphatic polyisocyanates, aromatic polyisocyanates, trifunctional isocyanates, isocyanate adducts and a combination thereof.

11 . The coating composition of claim 1 , wherein said crosslinking agent is selected from the group consisting of isophorone diisocyanate, toluene diisocyanate, hexamethylene diisocyanate, diphenylmethane diisocyanate, triphenyl triisocyanate, benzene triisocyanate, toluene triisocyanate, the trimer of hexamethylene diisocyanate, and a combination thereof.

12 . The coating composition of claim 1 further comprising one or more pigments.

13 . The coating composition of claim 1 further comprising one or more solvents, ultraviolet light stabilizers, ultraviolet light absorbers, antioxidants, hindered amine light stabilizers, leveling agents, rheological agents, thickeners, antifoaming agents, wetting agents, catalysts, or a combination thereof.

14 . A substrate coated with the coating composition of claim 1 .

15 . A process for coating a substrate having at least one existing coating layer thereon, said process comprising the steps of:

(A) applying a coating composition over said existing coating layer to form an overlay coating layer, wherein said coating composition comprises a film forming binder consisting essentially of:

(i) an acrylic polymer having one or more crosslinkable functional groups and having a glass transition temperature (Tg) of in a range of from −40° C. to 5° C.;

(ii) a polytrimethylene ether diol having a Mn (number average molecular weight) in a range of from 500 to 10,000; and

(iii) a crosslinking component containing at least one crosslinking agent having one or more crosslinking functional groups; and

(B) curing said overlay coating layer to form an overlay coating on said substrate.

16 . The process of claim 15 , wherein the polytrimethylene ether diol has a Mn in a range of from 500 to 4,000, a Tg of about −75° C. and a hydroxyl number in a range of from 20 to 200.

17 . The process of claim 15 , wherein the polytrimethylene ether diol is a blend of high and low molecular weight ether diols wherein the high molecular weight diol has an Mn in a range of from 1,000 to 4,000 and the low molecular weight diol has an Mn in a range of from 150 to 500 and the average Mn of the blend is in a range of from 1,000 to 3,000.

18 . The process of claim 15 , wherein at least one of said one or more crosslinkable functional groups is hydroxyl groups, and wherein at least one of said one or more crosslinking functional groups is isocyanate group.

19 . The process of claim 15 , wherein said existing coating layer is an epoxy primer layer.

20 . A substrate coated with the process of claim 15 .

Assignments (7)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 21, 2013
From: YOKOYAMA, AYUMU; SORMANI, PATRICIA MARY ELLEN; MA, SHEAU-HWA; ADAMS, JAMES LAMONTE
To: E. I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 030843/0955 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2013
From: YOKOYAMA, AYUMU; MA, SHEAU-HWA; SORMANI, PATRICIA MARY ELLEN; ADAMS, JAMES LAMONTE
To: E. I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 030843/0602 →
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 →