IP Library Granted Patent US 7,671,097
Granted Patent B2
US 7,671,097 · App. 11/135,635 · Granted Mar 2, 2010

Stable phenolic resin polymer dispersions having low free aldehyde content

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Quick Facts
Patent No.
US 7,671,097
App. No.
11/135,635
Granted
Mar 2, 2010
Kind
B2
Abstract

Stable dispersions of phenolic resins, particularly bisphenol-A/formaldehyde resins, for use in e.g., baking enamels, coatings, adhesives, binders, etc., are disclosed. The dispersions have low levels (e.g., <0.1% by weight) of free aldehyde, thereby reducing environmental harms associated with aldehyde emissions. Low free aldehyde levels are achieved using melamine as an aldehyde scavenger during preparation. It has now been discovered that melamine, in contrast to other scavengers of aldehydes, does not adversely affect dispersion stability, interfere with later processing operations, or negatively impact the final resin product quality (e.g., after curing).

Claims (37)

1. A method for making a storage stable aqueous dispersion of a phenolic resin, said method comprising:

(a) reacting an aromatic alcohol and an aldehyde in the presence of an oxide or hydroxide of an alkali metal or an alkaline earth metal as the primary catalyst to form a heat reactive phenolic resin containing less than about 5% by weight free aldehyde;

(b) adding a coupling solvent to said heat reactive phenolic resin to form a phenolic resin solution;

(c) adding melamine to said phenolic resin solution in an amount of about 1 to about 10 molar equivalents per mole of free aldehyde sufficient to react with said free aldehyde and yield a phenolic resin solution having a reduced content of free aldehyde; and

(d) adding polyvinyl alcohol as a protective colloid and water to said phenolic resin solution to form said storage stable dispersion from said phenolic resin solution having a reduced content of free aldehyde.

2. The method of claim 1 , wherein said aromatic alcohol is bisphenol-A, said aldehyde is formaldehyde, and said phenolic resin is a bisphenol-A/formaldehyde resole.

3. The method of claim 2 , wherein, after adding melamine in step (b), said reduced content of free formaldehyde in said bisphenol-A/formaldehyde resole is less than about 2% by weight.

4. The method of claim 3 , wherein said storage stable dispersion has a free formaldehyde content of less than about 0.1% by weight.

5. The method of claim 2 , wherein, in step (a), said bisphenol-A/formaldehyde resole is formed at a temperature from about 50° C. to about 150° C. for a time from about 15 minutes to about 3 hours, and in the presence of an alkaline catalyst.

6. The method of claim 2 , wherein, after step (b), said bisphenol-A/formaldehyde resole having a reduced content of free formaldehyde is acidified and heated to a temperature from about 50° C. to about 110° C.

7. An aqueous dispersion of a phenolic resin, made by the method of claim 1 , wherein said dispersion is storage stable for at least about 3 months.

8. The dispersion of claim 7 , wherein said dispersion is storage stable for at least about 6 months.

9. The dispersion of claim 8 , wherein said dispersion is storage stable for at least about 1 year.

10. The dispersion of claim 7 , wherein said aromatic alcohol is bisphenol-A, and said phenolic resin is a bisphenol-A/formaldehyde resole.

11. The dispersion of claim 7 , wherein said dispersion has a free formaldehyde content of less than about 0.1% by weight.

12. The dispersion of claim 7 , wherein said heat reactive phenolic resin is the reaction product of bisphenol-A and formaldehyde, wherein the molar ratio of formaldehyde to aromatic rings in the bisphenol-A is from about 0.85:1 to about 3:1.

13. The dispersion of claim 7 , wherein said dispersion has a solids content from about 40% to about 60% by weight and a viscosity from about 2000 to about 6000 cp at 25° C.

14. The dispersion of claim 7 , wherein said dispersion comprises a protective colloid and a coupling solvent.

15. The dispersion of claim 7 , wherein said aldehyde is formaldehyde.

16. The method of claim 1 , wherein, in step (b), melamine is added in an amount from about 3 to about 8 molar equivalents per mole of free formaldehyde contained in said phenolic resin.

17. The method of claim 1 , wherein, in step (b), melamine is reacted with free formaldehyde at a temperature from about 50° C. to about 100° C. under alkaline conditions.

18. A storage stable aqueous dispersion of a phenolic resin, said dispersion comprising:

(I) the reaction product of

(a) a heat reactive phenolic resin that is the reaction product, in the presence of an oxide or hydroxide of an alkali metal or an alkaline earth metal as the primary catalyst, of an aromatic alcohol and formaldehyde at a molar ratio of formaldehyde to aromatic rings in the aromatic alcohol from about 0.85:1 to about 3:1, wherein said heat reactive phenolic resin contains less than about 5% by weight free formaldehyde, and

(b) melamine, added to said heat reactive phenolic resin in an amount from about 1 to about 10 molar equivalents per mole of free formaldehyde contained in said phenolic resin, and reacted with said heat reactive phenolic resin at a temperature from about 50° C. to about 100° C. under alkaline conditions;

(II) a coupling solvent;

(III) polyvinyl alcohol as a protective colloid; and

(IV) water,

wherein (I), (II), (III), and (IV) are blended to yield said storage stable aqueous dispersion, having a free formaldehyde content of less than about 0.1% by weight.

19. A method for making a storage stable aqueous dispersion of a phenolic resin, said method comprising:

(a) reacting an aromatic alcohol and an aldehyde in the presence of an oxide or hydroxide of an alkali metal or an alkaline earth metal as the primary catalyst to form a heat reactive phenolic resin containing less than about 5% by weight free aldehyde;

(b) adding a coupling solvent to said heat reactive phenolic resin to form a phenolic resin solution;

(c) adding melamine to said phenolic resin solution in an amount of about 1 to about 10 molar equivalents per mole of free aldehyde sufficient to react with said free aldehyde and yield a phenolic resin solution having a reduced content of free aldehyde;

(d) adding an acid to said phenolic resin solution having a reduced content of free aldehyde, and

(e) adding polyvinyl alcohol as a protective colloid and water to said phenolic resin solution of step (d) to form said storage stable dispersion from said phenolic resin solution having a reduced content of free aldehyde.

20. An aqueous dispersion of a phenolic resin, made by the method of claim 19 .

21. The dispersion of claim 20 , wherein said aromatic alcohol is bisphenol-A, and said phenolic resin is a bisphenol-A/formaldehyde resole.

Assignments (8)
ASSIGNMENT OF PATENT AND TRADEMARK SECURITY INTEREST Recorded May 12, 2025
From: MACQUARIE CAPITAL FUNDING LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 071276/0379 →
CHANGE OF NAME Recorded Mar 13, 2025
From: GEORGIA-PACIFIC CHEMICALS LLC
To: BAKELITE CHEMICALS LLC
Reel/Frame 070495/0222 →
SECURITY INTEREST Recorded Jun 9, 2022
From: GEORGIA-PACIFIC CHEMICALS LLC; GEORGIA-PACIFIC CONSUMER PRODUCTS LP; ENERG2 TECHNOLOGIES, INC.; KOCH AGRONOMIC SERVICES LLC; BAKELITE UK HOLDING LTD.; SURFACE TECH LLC
To: GOLDMAN SACHS BANK USA, AS ADMINISTRATIVE AGENT
Reel/Frame 060328/0250 →
SECURITY INTEREST Recorded Jun 9, 2022
From: GEORGIA-PACIFIC CHEMICALS LLC; GEORGIA-PACIFIC CONSUMER PRODUCTS LP; ENERG2 TECHNOLOGIES, INC.; KOCH AGRONOMIC SERVICES LLC; BAKELITE UK HOLDING LTD.
To: MACQUARIE CAPITAL FUNDING LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 060328/0327 →
RELEASE OF SECURITY AGREEMENT Recorded May 16, 2013
From: CITICORP NORTH AMERICA, INC.
To: GEORGIA-PACIFIC LLC, DELAWARE LIMITED PARTNERSHIP; GEORGIA-PACIFIC CONSUMER PRODUCTS LP, DELAWARE LIMITED LIABILITY COMPANY; GEORGIA-PACIFIC CORRUGATED LLC, DELAWARE LIMITED LIABILITY COMPANY; DIXIE CONSUMER PRODUCTS LLC, DELAWARE LIMITED LIABILITY COMPANY; GEORGIA-PACIFIC GYPSUM LLC, DELAWARE LIMITED LIABILITY COMPANY; GEORGIA-PACIFIC CHEMICALS LLC, DELAWARE LIMITED LIABILITY COMPANY; GEORGIA-PACIFIC WOOD PRODUCTS LLC, DELAWARE LIMITED LIABILITY COMPANY; COLOR-BOX LLC, DELAWARE LIMITED LIABILITY COMPANY; GP CELLULOSE GMBH, ZUG, SWITZERLAND LIMITED LIABILITY COMPANY
Reel/Frame 030669/0958 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2007
From: GEORGIA-PACIFIC RESINS, INC.
To: GEORGIA-PACIFIC CHEMICALS LLC
Reel/Frame 018883/0713 →
SECURITY AGREEMENT Recorded Feb 23, 2006
From: ASHLEY, DREW & NORTHERN RAILWAY COMPANY; BROWN BOARD HOLDING, INC.; CP&P, INC.; COLOR-BOX, LLC; FORT JAMES CORPORATION; FORT JAMES MAINE, INC.; FORT JAMES OPERATING COMPANY; FORT JAMES GREEN BAY L.L.C.; PRIM COMPANY L.L.C.; KMHC, INCORPORATED; GEORGIA-PACIFIC FOREIGN HOLDINGS, INC.; GEORGIA-PACIFIC RESINS, INC.; GEORGIA-PACIFIC WEST, INC.; GEORGIA-PACIFIC FINANCE, LLC; GREAT NORTHERN NEKOOSA CORPORATION; LEAF RIVER FOREST PRODUCTS, INC.; NEKOOSA PACKAGING CORPORATION; MILLENNIUM PACKAGING SOLUTIONS, LLC; SOUTHWEST MILLWORK AND SPECIALTIES, INC.; WEST GEORGIA MANUFACTURING COMPANY; BLUE RAPIDS RAILWAY COMPANY; BRUNSWICK PULP LAND COMPANY, INC.; CECORR, INC.; ENCADRIA STAFFING SOLUTIONS, INC.; FORT JAMES INTERNATIONAL HOLDINGS, LTD.; GEORGIA-PACIFIC INVESTMENT, INC.; FORT JAMES CAMAS L.L.C.; FORT JAMES NORTHWEST L.L.C.; G-P GYPSUM CORPORATION; GEORGIA-PACIFIC CHILDCARE CENTER, LLC; GEORGIA-PACIFIC HOLDINGS, INC.; G-P OREGON, INC.; GEORGIA-PACIFIC ASIA, INC.; GLOSTER SOUTHERN RAILROAD COMPANY; GREAT SOUTHERN PAPER COMPANY; OLD PINE BELT RAILROAD COMPANY; NEKOOSA PAPERS INC.; TOMAHAWK LAND COMPANY; XRS, INC.; PHOENIX ATHLETIC CLUB, INC.; KOCH RENEWABLE RESOURCES, LLC; KOCH FOREST PRODUCTS HOLDING, LLC; KOCH WORLDWIDE INVESTMENTS, INC.; OLD AUGUSTA RAILROAD, LLC; BRUNSWICK CELLULOSE, INC.; LEAF RIVER CELLULOSE, LLC; KOCH CELLULOSE AMERICA MARKETING, LLC; KOCH CELLULOSE, LLC; BLUEYELLOW, LLC
To: CITICORP NORTH AMERICA, INC.
Reel/Frame 017626/0205 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 26, 2005
From: BOYER, MR. PETER C.; IMAN, MR. AHMED A.
To: GEORGIA-PACIFIC RESINS, INC.
Reel/Frame 016307/0607 →