IP Library Granted Patent US 7,060,745
Granted Patent B2
US 7,060,745 · App. 10/121,396 · Granted Jun 13, 2006

Waterborne acrylate-functionalized alkyd coating compositions

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Quick Facts
Patent No.
US 7,060,745
App. No.
10/121,396
Granted
Jun 13, 2006
Kind
B2
Abstract

A waterborne acrylate-functionalized alkyd coating composition is disclosed, which includes an acrylate-functionalized alkyd resin, at least one drier, and water. The acrylate-functionalized alkyd resin comprises the reaction product of (i) a hydroxy functional alkyd resin, (ii) an acid anhydride, and (iii) a glycidyl acrylate. Methods of preparing waterborne acrylate-functionalized alkyd coating compositions are also disclosed.

Claims (57)

1. A waterborne acrylate-functionalized alkyd coating composition, comprising:

(I) an acrylate-functionalized alkyd resin comprising the reaction product of:

(a) about 79 to about 95 wt % of an alkyd resin having an acid number of from 0 to about 100 mg KOH/g;

(b) about 2 to about 8 wt % of an acid anhydride; and

(c) about 3 to about 13 wt % of a glycidyl acrylate, wherein the glycidyl moiety of the glycidyl acrylate is the reactive moiety and the reaction product contains reactive acrylate moieties, and

wherein the weight percents are based on the total weight of (a), (b) and (c);

(II) at least one drier; and

(III) water.

2. The waterborne acrylate-functionalized alkyd coating composition of claim 1 , wherein the alkyd resin of (I)(a) comprises the reaction product of:

(i) 0 to about 30 mol % of a diol;

(ii) about 10 to about 40 mol % of a polyol;

(iii) about 20 to about 40 mol % of a polyacid;

(iv) 0 to about 10 mol % of a monofunctional acid; and

(v) about 10 to about 50 mol % of a fatty acid, fatty ester or naturally occurring oil,

wherein the mole percents are based on the total moles of (i), (ii), (iii), (iv) and (v).

3. The waterborne acrylate-functionalized alkyd coating composition of claim 1 , wherein the glycidyl acrylate is glycidyl methacrylate.

4. The waterborne acrylate-functionalized alkyd coating composition of claim 1 , wherein the alkyd resin has a hydroxyl number from about 30 to about 180 mg KOH/g.

5. The waterborne acrylate-functionalized alkyd coating composition of claim 2 , wherein the alkyd resin of (I)(a) further comprises from about 2 to about 10 mol % of a sulfomonomer.

6. The waterborne acrylate-functionalized alkyd coating composition of claim 2 , wherein the diol is neopentyl glycol, the polyol is trimethylolpropane or pentaerythritol, the polyacid is isophthalic acid or phthalic anhydride, and the naturally occurring oil or fatty acid is soybean oil or tall oil fatty acid.

7. The waterborne acrylate-functionalized alkyd coating composition of claim 5 , wherein the sulfomonomer comprises 5-sodiosulfoisophthalic acid.

8. The waterborne acrylate-functionalized alkyd coating composition of claim 1 , wherein:

the acrylate-functionalized alkyd resin is present in an amount of from about 30 to about 60 wt %, based on the total composition;

the drier is present in an amount of from about 0.01 to about 1.0 wt %, based on the total composition; and

the water is present in about 40 to about 70 wt %, based on the total composition.

9. The waterborne acrylate-functionalized alkyd coating composition of claim 1 , wherein the drier comprises at least one member selected from the group consisting of a cobalt salt, a zirconium salt, a calcium salt, a zinc salt, and a manganese salt.

10. The waterborne acrylate-functionalized alkyd coating composition of claim 1 , further comprising an amine.

11. The waterborne acrylate-functionalized alkyd coating composition of claim 1 , further comprising a surfactant.

12. The waterborne acrylate-functionalized alkyd coating composition of claim 1 , further comprising from greater than 0 to about 30 wt %, based on the total composition, of an organic solvent.

13. The waterborne acrylate-functionalized alkyd coating composition of claim 1 , further comprising at least one member selected from the group consisting of a flow control agent, an extender, a plasticizer, a flatting agent, a pigment wetting agent, a pigment dispersing agent, an ultraviolet (UV) absorber, a UV light stabilizer, a tinting pigment, a colorant, a defoaming agent, an antifoaming agent, an anti-settling agent, an anti-sag agent, a bodying agent, an anti-skinning agent, an anti-flooding agent, an anti-floating agent, and a corrosion inhibitor.

14. A method of making a waterborne acrylate-functionalized alkyd coating composition, comprising a step of combining:

(I) an acrylate-functionalized alkyd resin comprising the reaction product of

(a) a hydroxyl functional alkyd resin with an acid number of 0 to about 100 mg KOH/g,

(b) an acid anhydride, and

(c) a glycidyl acrylate,

wherein the glycidyl moiety of the glycidyl acrylate is the reactive moiety and the reaction product contains reactive acrylate moieties;

(II) at least one drier; and

(III) water.

15. The method according to claim 14 , wherein:

the acrylate-functionalized alkyd resin is present in an amount of from about 30 to about 60 wt %, based on the total composition;

the drier is present in an amount of from about 0.01 to about 1.0 wt %, based on the total composition; and

the water is present in an amount of from about 40 to about 70 wt %, based on the total composition.

16. The method of claim 15 , further comprising a step of adding a surfactant.

17. A method of making a waterborne acrylate-functionalized alkyd coating composition, comprising the steps of:

(a) reacting:

(i) from 0 to about 30 mol % of a diol,

(ii) from about 10 to about 40 mol % of a polyol,

(iii) from about 20 to about 40 mol % of a polyacid,

(iv) from 0 to about 10 mol % of a monofunctional acid, and

(v) from about 10 to about 50 mol % of a fatty acid, a fatty ester, or a naturally occurring, partially-saponified oil,

in the presence of a catalyst, each as described above, at about 180-250° C., until the desired amount of the condensate is obtained, to form an alkyd resin, wherein the mole percents are based on the total moles of (i), (ii), (iii), (iv), (v) and (vi);

(b) reacting, at a temperature range of about 150-165° C., the alkyd resin of step (a) with from about 2 to about 8 wt % of an acid anhydride, to form a carboxyl-functional alkyd resin; and

(c) reacting, at a temperature range of from about 125-155° C., the carboxyl-functional alkyd resin of step (b) with from about 3 to about 12 wt % of a glycidyl acrylate, to form an acrylate-functionalized alkyd resin,

wherein the weight percents are based on the total weight of the alkyd resin, the acid anhydride and the glycidcyl acrylate.

18. A substrate coated with the waterborne acrylate-functionalized alkyd coating composition of claim 1 .

19. A substrate coated with the waterborne acrylate-functionalized alkyd coating composition of claim 8 .

20. A substrate coated with a waterborne acrylate-functionalized alkyd coating composition of claim 12 .

21. A method of making an emulsion of the acrylate-functionalized alkyd resin of claim 1 , comprising a step of combining the acrylate-functionalized alkyd resin with at least one surfactant, in the presence of water.

Assignments (25)
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (030146/0970) Recorded Jul 9, 2019
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
To: HEXION INC. (FORMERLY KNOWN AS MOMENTIVE SPECIALTY CHEMICALS INC.)
Reel/Frame 049706/0264 →
RELEASE OF SECURITY INTEREST Recorded Feb 23, 2017
From: WILMINGTON TRUST, NATIONAL ASSOCIATION (SUCCESSOR BY MERGER TO WILMINGTON TRUST FSB), AS COLLATERAL AGENT
To: HEXION INC. (FORMERLY KNOWN AS HEXION SPECIALTY CHEMICALS INC.); BORDEN CHEMICAL FOUNDRY, LLC; HEXION INVESTMENTS INC. (FORMERLY KNOWN AS BORDEN CHEMICAL INVESTMENTS, INC.); HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; HEXION INTERNATIONAL INC. (FORMERLY KNOWN AS BORDEN CHEMICAL INTERNATIONAL INC.); OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
Reel/Frame 041793/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2017
From: HEXION INC.
To: SYNTHOMER USA LLC.
Reel/Frame 041057/0634 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: HEXION INC.
Reel/Frame 039259/0696 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 039260/0011 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 039260/0069 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 039260/0158 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 039259/0940 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: HEXION INC.
Reel/Frame 039258/0913 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: WILMINGTON TRUST COMPANY
To: HEXION INC.
Reel/Frame 039259/0628 →
RELEASE OF SECURITY INTEREST Recorded Jul 15, 2016
From: WILMINGTON TRUST COMPANY
To: HEXION INC.
Reel/Frame 039360/0724 →
CHANGE OF NAME Recorded Jan 29, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: HEXION INC.
Reel/Frame 034859/0314 →
PATENT SECURITY AGREEMENT Recorded Apr 3, 2013
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 030146/0946 →
PATENT SECURITY AGREEMENT Recorded Apr 3, 2013
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 030146/0970 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Mar 28, 2013
From: JPMORGAN CHASE BANK, N.A.
To: MOMENTIVE SPECIALTY CHEMICALS INC. (F/K/A HEXION SPECIALTY CHEMICALS, INC.)
Reel/Frame 030111/0021 →
MERGER Recorded Mar 5, 2012
From: RESOLUTION SPECIALTY MATERIALS LLC
To: HEXION SPECIALTY CHEMICALS, INC.
Reel/Frame 027805/0616 →
CHANGE OF NAME Recorded Mar 5, 2012
From: HEXION SPECIALTY CHEMICALS, INC.
To: MOMENTIVE SPECIALTY CHEMICALS INC.
Reel/Frame 027805/0865 →
SECURITY AGREEMENT Recorded Feb 5, 2010
From: HEXION LLC; HEXION SPECIALTY CHEMICALS, INC.; BORDEN CHEMICAL FOUNDRY, LLC; BORDEN CHEMICAL INVESTMENTS, INC.; HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; BORDEN CHEMICAL INTERNATIONAL, INC.; OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 023905/0451 →
SECURITY INTEREST Recorded Jan 29, 2010
From: HEXION SPECIALTY CHEMICALS, INC.; BORDEN CHEMICAL FOUNDRY, LLC; BORDEN CHEMICAL INVESTMENTS, INC.; HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; BORDEN CHEMICAL INTERNATIONAL, INC.; OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
To: WILMINGTON TRUST FSB, AS COLLATERAL AGENT
Reel/Frame 023963/0038 →
SECURITY AGREEMENT Recorded Nov 21, 2006
From: HEXION SPECIALTY CHEMICALS, INC.
To: JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT
Reel/Frame 018535/0556 →
SECURITY AGREEMENT Recorded Nov 21, 2006
From: HEXION SPECIALTY CHEMICALS, INC.
To: WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT
Reel/Frame 018535/0701 →
SECURITY AGREEMENT Recorded Jul 14, 2006
From: HEXION SPECIALTY CHEMICALS, INC.
To: JPMORGAN CHASE BANK, N.A. AS COLLATERAL AGENT
Reel/Frame 017946/0151 →
SECURITY AGREEMENT Recorded Aug 31, 2005
From: RESOLUTION PERFORMANCE PRODUCTS LLC; RESOLUTION SPECIALTY MATERIALS LLC; BORDEN CHEMICAL, INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 016480/0648 →
SECURITY AGREEMENT Recorded Aug 31, 2005
From: RESOLUTION PERFORMANCE PRODUCTS LLC; RESOLUTION SPECIALTY MATERIALS LLC; BORDEN CHEMICAL, INC.
To: WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT
Reel/Frame 016522/0428 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2004
From: EASTMAN CHEMICAL COMPANY
To: RESOLUTION SPECIALTY MATERIALS LLC
Reel/Frame 015201/0335 →