IP Library Granted Patent US 8,241,415
Granted Patent B2
US 8,241,415 · App. 11/473,734 · Granted Aug 14, 2012

Wax formulations for lignocellulosic products, methods of their manufacture and products formed therefrom

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Quick Facts
Patent No.
US 8,241,415
App. No.
11/473,734
Granted
Aug 14, 2012
Kind
B2
Abstract

The present invention is directed to a wax formulation for use in lignocellulosic products, which impart improved properties such as dimensional stability when the products are exposed to moisture. The wax formulations include a wax and a surface tension/interfacial tension reducing agent comprising one or more of a fluorinated compound having two to six carbon atoms, an alkylphenol alkoxylate or an ethoxylated acetylenic diol.

Claims (64)

1. A wax emulsion comprising, based on the total weight of the emulsion:

about 25 to about 80 wt % of water;

about 20 to about 60 wt % of a wax component;

about 0.5 to about 5 wt % of an emulsion stabilizing component, wherein the emulsion stabilizing component is derived from a carboxylic acid and an aminoalcohol; and

a surface tension/interfacial tension reducing agent, wherein the surface tension/interfacial tension reducing agent comprises:

an alkylphenol alkoxylate, present in an amount of 0.0125 to 0.075 wt %;

a C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms, present in an amount of 0.025 to 0.075 wt %; and

a combination of a C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms and a siloxane, present in an amount of 0.025 to 0.075 wt %.

2. The emulsion of claim 1 , wherein alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms and a siloxane is present in an amount of 0.03 to 0.05 wt %.

3. The emulsion of claim 1 , wherein the carboxylic acid is stearic acid and the aminoalcohol is triethanolamine.

4. A method for making a wax emulsion, comprising:

combining an emulsifiable wax, an aqueous medium, and an emulsion stabilizer to form a mixture;

agitating the mixture to form an emulsion; and then

adding a surface tension/interfacial tension reducing agent after the emulsion is formed, wherein the surface tension/interfacial tension reducing agent comprises an alkylphenol alkoxylate, a C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms, a combination of a C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms and a siloxane, wherein the emulsion comprises, based on the total weight of the emulsion:

about 25 to about 80 wt % of water;

about 20 to about 60 wt % of emulsifiable wax;

about 0.5 to about 5 wt % of the emulsion stabilizing component; and

a surface tension/interfacial tension reducing agent, wherein the surface tension/interfacial tension reducing agent comprises:

an alkylphenol alkoxylate, present in an amount of 0.0125 to 0.075 wt %;

a C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms, present in an amount of 0.025 to 0.075 wt %; and

a combination of a C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms and a siloxane, present in an amount of 0.025 to 0.075 wt %.

5. The method of claim 4 , wherein alkoxylated substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms and a siloxane is present in an amount of 0.03 to 0.05 wt %.

6. The method of claim 4 , wherein the emulsion stabilizing component is derived from a carboxylic acid and an aminoalcohol.

7. The method of claim 6 , wherein the carboxylic acid is stearic acid and the aminoalcohol is triethanolamine.

8. A lignocellulosic composite, comprising:

a mixture of:

a lignocellulosic material; and

a wax emulsion comprising:

water;

a wax component;

an emulsion stabilizing component, wherein the emulsion stabilizing component is derived from a carboxylic acid and an aminoalcohol; and

a surface tension/interfacial tension reducing agent, wherein the surface tension/interfacial tension reducing agent comprises:

an alkylphenol alkoxylate,

a C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms, and

a combination of a C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms and a siloxane.

9. The lignocellulosic composite of claim 8 further comprising a cured adhesive binder.

10. The wax emulsion of claim 1 , further comprising a cured adhesive binder.

11. The lignocellulosic composite of claim 8 , wherein the wax emulsion comprises, based on the total weight of the emulsion:

about 25 to about 80 wt % of water;

about 20 to about 60 wt % of a wax component;

about 0.5 to about 5 wt % of an emulsion stabilizing component;

0.0125 wt % to 0.075 wt % of an alkylphenol alkoxylate;

0.025 wt % to 0.075 wt % of a C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms; and

0.025 wt % to 0.075 wt % of a combination of a C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms and a siloxane.

12. The lignocellulosic composite of claim 11 , further comprising a cured adhesive binder.

13. The lignocellulosic composite of claim 8 , wherein the lignocellulosic material comprises a material selected from the group consisting of wood fibers, wood flakes, wood strands, wood chips, wood particles, pulp wood, wood wastes, wood bark, saw dust, paper, chips, cellulose-containing fibers of annual plants, granulated biomasses, recycled synthetic rubber, recycled natural rubber, recycled wood fiber, waste fibers, the grinding dust of the boards produced, and mixtures thereof.

14. The lignocellulosic composite of claim 9 , wherein the wax emulsion comprises between about 0.1 and about 10 wt % based on the total weight of the wax formulation and cured adhesive binder.

15. A wax emulsion, consisting essentially of:

water;

a wax component;

an emulsion stabilizing component, wherein the emulsion stabilizing component is derived from a carboxylic acid and an aminoalcohol; and

a surface tension/interfacial tension reducing agent, wherein the surface tension/interfacial tension reducing agent comprises:

an alkylphenol alkoxylate;

a first C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms; and

a combination of a second C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms and a siloxane.

16. The wax emulsion of claim 15 , wherein the wax emulsion comprises:

about 25 to about 80 wt % of water;

about 20 to about 60 wt % of a wax component;

about 0.5 to about 5 wt % of an emulsion stabilizing component;

0.0125 wt % to 0.075 wt % of the alkylphenol alkoxylate;

0.025 wt % to 0.075 wt % of the first C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms, present in an amount of 0.025 to 0.075 wt %; and

0.025 wt % to 0.075 wt % of the combination of the second C 2 -C 3 alkoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms and a siloxane.

17. The wax emulsion of claim 15 , wherein the ethoxylated, substantially symmetrical acetylenic diol having 6 to about 100 carbon atoms and a siloxane is present in an amount of 0.03 to 0.05 wt %.

18. The wax emulsion of claim 15 , wherein the acid is stearic acid and the aminoalcohol is triethanolamine.

Assignments (21)
RELEASE OF SECURITY INTEREST IN PATENTS (TERM LOAN) RECORDED AT REEL/FRAME 049741/0425 Recorded Mar 18, 2022
From: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
To: HEXION INC.
Reel/Frame 059435/0473 →
RELEASE OF SECURITY INTEREST IN PATENTS (ABL) RECORDED AT REEL/FRAME 049740/0770 Recorded Mar 18, 2022
From: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
To: HEXION INC.
Reel/Frame 059435/0490 →
SECURITY INTEREST Recorded Mar 18, 2022
From: HEXION INC.; HEXION INVESTMENTS INC.
To: GOLDMAN SACHS BANK USA, AS ADMINISTRATIVE AGENT
Reel/Frame 059436/0748 →
SECURITY INTEREST Recorded Mar 18, 2022
From: HEXION INC.; HEXION INVESTMENTS INC.
To: GOLDMAN SACHS BANK USA, AS ADMINISTRATIVE AGENT
Reel/Frame 059436/0823 →
SECURITY INTEREST Recorded Mar 18, 2022
From: HEXION INC.; HEXION INVESTMENTS INC.
To: ROYAL BANK OF CANADA, AS ADMINISTRATIVE AGENT
Reel/Frame 059436/0842 →
PATENT SECURITY INTEREST (ABL) Recorded Jul 12, 2019
From: HEXION INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 049740/0770 →
PATENT SECURITY INTEREST (TERM LOAN) Recorded Jul 12, 2019
From: HEXION INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 049741/0425 →
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 →
PATENT SECURITY INTEREST ASSIGNMENT AGREEMENT Recorded Apr 3, 2019
From: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS THE PRIOR COLLATERAL AGENT
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS THE CURRENT COLLATERAL AGENT
Reel/Frame 048788/0617 →
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 →
SECURITY INTEREST Recorded Feb 13, 2017
From: HEXION INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 041693/0888 →
CHANGE OF NAME Recorded Feb 3, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: HEXION INC.
Reel/Frame 034882/0127 →
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 →
CHANGE OF NAME Recorded Apr 15, 2011
From: HEXION SPECIALTY CHEMICALS, INC.
To: MOMENTIVE SPECIALTY CHEMICALS INC.
Reel/Frame 026138/0817 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 21, 2006
From: WANTLING, STEVEN J.; ZEPKA, BONNIE; GRENO, MICHAEL A.; DONLON, THOMAS MICHAEL
To: HEXION SPECIALTY CHEMICALS, INC.
Reel/Frame 018294/0602 →