IP Library Granted Patent US 11,780,112
Granted Patent B2
US 11,780,112 · App. 17/145,976 · Granted Oct 10, 2023

Binders containing an aldehyde-based resin and an isocyanate-based resin and methods for making composite lignocellulose products therefrom

Inventors: Juan José Joaquin Valenzuela Valdés (San Pedro de la Paz, CL); Ildolfo Alfonso Duran Retamal (Los Ángeles, CL); Carlos Roberto Maldonado Rodríguez (Tome, CL); Bobby Lee Williamson (Conyers, GA)
B27N1/0209C08G8/26C08K3/22C08K5/21C08L61/14C08L61/32C08L97/02C08G18/7671C08L2310/00
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Quick Facts
Patent No.
US 11,780,112
App. No.
17/145,976
Granted
Oct 10, 2023
Kind
B2
Abstract

Binders, methods for making same, and methods for making composite lignocellulose products therefrom. The binder can include about 30 wt % to about 40 wt % of solids that include a urea-modified aldehyde-based resin; about 0.1 wt % to about 3 wt % of solids that include an isocyanate-based resin; about 0.1 wt % to about 12 wt % of an extender; and about 50 wt % to about 62 wt % of water, where all weight percent values are based on a total weight of the binder. The binder can have a sodium hydroxide equivalent weight alkalinity of about 3 wt % to about 9 wt %.

Claims (35)

1. A binder for making composite lignocellulose products, comprising:

about 32 wt % to about 38 wt % of solids comprising a urea-modified aldehyde-based resin, wherein the urea-modified aldehyde-based resin comprises a urea-modified phenol-formaldehyde resin having a formaldehyde to phenol molar ratio of about 1.8:1 to about 2.6:1;

about 1 wt % to about 2 wt % of solids comprising an isocyanate-based resin;

about 2.9 wt % to about 5.2 wt % of an extender; and

about 53 wt % to about 58 wt % of a liquid medium, wherein the binder comprises 4 wt % to about 9.5 wt % of free urea, mono-methylol urea, di-methylol urea, tri-methylol urea, urea covalently bonded with a carbon atom derived from an aldehyde during synthesis of the urea-modified aldehyde-based resin, or a mixture thereof, wherein all weight percent values are based on a total weight of the binder, wherein the binder has a sodium hydroxide equivalent weight alkalinity of about 4.5 wt % to about 7.5 wt %, and wherein the binder is free of a surfactant.

2. The binder of claim 1 , wherein at least a portion of urea in the urea-modified aldehyde-based resin is in the form of free urea, mono-methylol urea, di-methylol urea, or tri-methylol urea, or a mixture thereof.

3. The binder of claim 1 , wherein at least a portion of urea in the urea-modified aldehyde-based resin is covalently bonded with a carbon atom derived from an aldehyde during synthesis of the urea-modified aldehyde-based resin.

4. The binder of claim 1 , wherein the urea-modified aldehyde-based resin further comprises a urea-modified melamine-formaldehyde resin, a urea-modified phenol-melamine-formaldehyde resin, a urea-modified resorcinol-formaldehyde resin, a urea-modified phenol-resorcinol-formaldehyde resin, or any mixture thereof.

5. The binder of claim 1 , wherein the binder comprises sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium carbonate, potassium carbonate, calcium carbonate, sodium borate, potassium borate, calcium borate, and zinc borate or a mixture thereof.

6. The binder of claim 1 , wherein the binder has a viscosity of ≤8,500 cP when maintained at a temperature of about 25° C. for at least 8 days after formation of the binder.

7. The binder of claim 1 , further comprising about 0.1 wt % to about 12 wt % of a filler, based on the total weight of the binder.

8. The binder of claim 7 , wherein the extender comprises wheat flour, corn flour, or a mixture thereof, and wherein the filler comprises corn cob residue, a nutshell flour, a fruit pit flour, or a mixture thereof.

9. A binder for making composite lignocellulose products, comprising:

about 32 wt % to about 38 wt % of solids comprising a urea-modified aldehyde-based resin, wherein the urea-modified aldehyde-based resin comprises a urea-modified phenol-formaldehyde resin having a formaldehyde to phenol molar ratio of about 1.8:1 to about 2.6:1;

about 1 wt % to about 2 wt % of solids comprising an isocyanate-based resin;

about 2.9 wt % to about 5.2 wt % of an extender;

about 0.01 wt % to about 0.5 wt % of a surfactant, wherein the surfactant comprises an acetylenic diol compound, ethylene glycol, or a mixture thereof; and

about 53 wt % to about 58 wt % of a liquid medium, wherein the binder comprises 4 wt % to about 9.5 wt % of free urea, mono-methylol urea, di-methylol urea, tri-methylol urea, urea covalently bonded with a carbon atom derived from an aldehyde during synthesis of the urea-modified aldehyde-based resin, or a mixture thereof, wherein all weight percent values are based on a total weight of the binder, and wherein the binder has a sodium hydroxide equivalent weight alkalinity of about 4.5 wt % to about 7.5 wt %.

10. The binder of claim 1 , further comprising about 0.05 wt % to about 3.5 wt % of a salt, based on the total weight of the binder, and wherein the salt comprises sodium chloride, potassium chloride, calcium chloride, sodium sulfate, potassium sulfate, calcium sulfate, magnesium sulfate, or a mixture thereof.

11. The binder of claim 1 , wherein the liquid medium comprises water.

12. The binder of claim 1 , further comprising about 0.1 wt % to about 12 wt % of a filler, based on the total weight of the binder, wherein at least a portion of the urea in the urea-modified phenol-formaldehyde resin is covalently bonded with a carbon atom derived from an aldehyde during synthesis of the urea-modified aldehyde-based resin, and at least a portion of the urea in the urea-modified phenol-formaldehyde resin is in the form of mono-methylol urea, in the form of di-methylol urea, or in the form of tri-methylol urea.

13. The binder of claim 1 , wherein:

a first portion of urea in the urea-modified aldehyde-based resin is covalently bonded with a carbon atom derived from an aldehyde during synthesis of the urea-modified aldehyde-based resin by adding the first portion of urea as a reactant during the synthesis of the urea-modified aldehyde-based resin, and

a second portion of urea in the urea-modified phenol-aldehyde resin is in the form of free urea added after the urea-modified aldehyde-based resin is synthesized.

14. The binder of claim 13 , wherein:

an amount of the first portion of urea added during the synthesis of the urea-modified aldehyde resin is at least 2 wt %, based on the total weight of the binder, and

an amount of the second portion of urea added after the urea-modified aldehyde-based resin is synthesized is at least 2 wt %, based on the total weight of the binder.

15. The binder of claim 1 , wherein the binder comprises 6 wt % to about 7.5 wt % of free urea, mono-methylol urea, di-methylol urea, tri-methylol urea, urea covalently bonded with a carbon atom derived from an aldehyde during synthesis of the urea-modified aldehyde-based resin, or a mixture thereof, based on the total weight of the binder.

16. A method for making a composite product, comprising:

combining a plurality of lignocellulose substrates and a binder to produce a resinated furnish, wherein the binder comprises:

about 32 wt % to about 38 wt % of solids comprising a urea-modified aldehyde-based resin, wherein the urea-modified aldehyde-based resin comprises a urea-modified phenol-formaldehyde resin having a formaldehyde to phenol molar ratio of about 1.8:1 to about 2.6:1;

about 1 wt % to about 2 wt % of solids comprising an isocyanate-based resin;

about 2.9 wt % to about 5.2 wt % of an extender; and

about 53 wt % to about 58 wt % of a liquid medium, wherein the binder comprises 4 wt % to about 9.5 wt % of free urea, mono-methylol urea, di-methylol urea, tri-methylol urea, urea covalently bonded with a carbon atom derived from an aldehyde during synthesis of the urea-modified aldehyde-based resin, or a mixture thereof, wherein all weight percent values are based on a total weight of the binder, wherein the binder has a sodium hydroxide equivalent weight alkalinity of about 4.5 wt % to about 7.5 wt %, and wherein the binder is free of a surfactant; and

heating the resinated furnish to a temperature of about 60° C. to about 300° C. to at least partially cure the binder to produce a composite lignocellulose product.

Assignments (8)
SECURITY INTEREST Recorded May 12, 2025
From: BAKELITE CHEMICALS LLC; BAKELITE UK HOLDING LTD.; BAKELITE GMBH; BAKELITE SYNTHETICS UK
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 071090/0740 →
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 →
SECURITY INTEREST Recorded Jan 23, 2025
From: BAKELITE CHEMICALS LLC; BAKELITE UK HOLDING LTD.; BAKELITE GMBH; BAKELITE SYNTHETICS UK LIMITED
To: GOLDMAN SACHS BANK USA
Reel/Frame 069981/0468 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY ADDRESS PREVIOUSLY RECORDED AT REEL: 061916 FRAME: 0934. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT . Recorded Oct 17, 2023
From: GEORGIA-PACIFIC CHEMICALS LLC
To: BAKELITE CHEMICALS LLC
Reel/Frame 065244/0901 →
CHANGE OF NAME Recorded Nov 10, 2022
From: GEORGIA-PACIFIC CHEMICALS LLC
To: BAKELITE CHEMICALS LLC
Reel/Frame 061916/0934 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2021
From: VALDÉS, JUAN JOSÉ JOAQUIN VALENZUELA; RETAMAL, IIDOLFO ALFONSO DURÁN; RODRÍGUEZ, CARLOS ROBERTO MALDONADO; WILLIAMSON, BOBBY L.
To: GEORGIA-PACIFIC CHEMICALS LLC
Reel/Frame 055407/0278 →
Continuity (3)
Continuation In Part 16302245
Provisional Application 62341717 · May 26, 2016
Related Publication 20210129375A1 · May 6, 2021