IP Library Granted Patent US 7,129,286
Granted Patent B2
US 7,129,286 · App. 10/416,745 · Granted Oct 31, 2006

Waterborne acrylic modified alkyd resins

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Quick Facts
Patent No.
US 7,129,286
App. No.
10/416,745
Granted
Oct 31, 2006
Kind
B2
Abstract

A process for preparing an acrylic-modified alkyd resin comprising the steps of: d) preparing a sulfonated alkyd resin product; e) preparing an acrylated fatty acid product; and f) reacting the product of step a) and the product of step b) under appropriate polymerization conditions, and for preparing a waterbome composition on the basis thereof as well as products obtainable by those processes.

Claims (22)

1. A process for preparing an acrylic-modified alkyd resin comprising the steps of:

a) preparing a sulfonated alkyd resin product;

b) preparing an acrylated fatty acid product; and

c) reacting the product of step a) and the product of step b) under appropriate polymerization conditions.

2. The process according to claim 1 , wherein the preparation of the product of step a) comprises the following steps:

i) reacting a polyol and a sulfomonomer to obtain a polyol sulfomonomer adduct, and ii) reacting a mixture comprising the polyol sulfomonomer adduct of step i), at least one fatty acid, and at least one polycarboxylic acid or anhydride to obtain the sulfonated alkyd resin product.

3. The process according to claim 2 , wherein the polyol used in step i) is trimethylolpropane, and the sulfomonomer of step i) is 5-sodiosulfoisophthalic acid.

4. The process according to any of the preceding claims, wherein the preparation of the product of step b) comprises reacting at least one fatty acid with at least one acrylic-functional monomer.

5. The process according to claim 1 , wherein the preparation of the product of step c) comprises reacting the product of step a) and the product of step b), together with an appropriate catalyst, under condensation polymerization conditions.

6. An acrylic-modified alkyd resin prepared by the process of claim 1 , wherein the acrylic-modified alkyd resin has an acid value of from 10 to 50 mg KOH/g an oil length of from 5 to 70%, a sulfur monomer content of from 2 to 7%, and an acrylic-functional monomer content of from 2 to 45%.

7. An acrylic-modified aalyd resin prepared by the process of claim 2 wherein the acrylic-modified alkyd resin has an acid value of from 10 to 50 mg KOH/g, an oil length of from 5 to 70%, a sulfur monomer content of from 2 to 7%, and an acrylic-functional monomer content of from 2 to 45%.

8. An acrylic-modified alkyd resin prepared by the process of claim 3 wherein the acrylic-modified alkyd resin has an acid value of from 10 to 50 mg KOH/g, an oil length of from 5 to 70%, a sulfur monomer content of from 2 to 7%, and an acrylic-functional monomer content of from 2 to 45%.

9. A process for preparing a waterborne acrylic-modified alkyd resin composition comprising: a) preparing an acrylic-modified alkyd resin prepared by the process of claim 1 ; and b) dissolving the product of step (a) in a solution of water and ammonia.

10. The process of claim 9 wherein the preparation of the product of step a) comprises the steps of:

i) reacting a polyol and a sulfomonomer to obtain a polyol sulfomonomer adduct, and

ii) reacting a mixture comprising the polyol sulfomonomer adduct of step i), at least one fatty acid, and at least one polycarboxylic acid or anhydride to obtain the sulfonated alkyd resin product.

11. The process of claim 10 , wherein the polyol used in step i) is trimethylolpropane, and the sulfomonomer of step i) is 5-sodiosulfoisophthalic acid.

12. A coating composition comprising a) a waterborne acrylic-modified alkyd resin composition prepared by the process of claim 9 ; and b) one additive selected from the group consisting of leveling rheology and flow control agents, extenders, reactive coalescing aids, plasticizers, flatting agents, pigment wetting and dispersing agents and surfactants, ultraviolet (UV) absorbers, UV light stabilizers, tinting pigments, colorants, defoaming and antifoaming agents, anti-settling, anti-sag and bodying agents, anti-skinning agents, anti-flooding and anti-floating agents, biocides, fungicides and mildewcides, corrosion inhibitors, thickening agents, and coalescing agents.

13. The coating composition of claim 12 wherein the preparation of the product step a) comprises the steps of:

i) reacting a polyol and a sulfomonomer to obtain a polyol sulfomonomer adduct, and

ii) reacting a mixture comprising the polyol sulfomonomer adduct of step i), at least one fatty acid, and at least one polycarboxylic acid or anhydride to obtain the sulfonated alkyd resin product.

14. The coating composition of claim 13 , wherein the polyol used in step i) is trimethylolpropane, and the sulfomonomer of step i) is 5-sodiosulfoisophthalic acid.

Assignments (14)
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 039259/0940 →
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 039260/0011 →
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 →
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 →