IP Library Granted Patent US 12,286,565
Granted Patent B2
US 12,286,565 · App. 17/622,368 · Granted Apr 29, 2025

Process for preparing a bonding resin

Inventors: Ashar Zafar (Älta, SE); Jesper Ekström (Johanneshov, SE)
Assignee: Stora Enso OYJ
C09J171/00B32B7/12B32B21/042B32B21/13B32B21/14C09J197/005B32B2255/08B32B2255/26B32B2419/00
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Quick Facts
Patent No.
US 12,286,565
App. No.
17/622,368
Granted
Apr 29, 2025
Kind
B2
Abstract

The present invention relates to a process for preparing a bonding resin, lignin in solid form or in the form of a dispersion in water is mixed with a crosslinker; and optionally one or more additives followed by addition of a basic solution. The bonding resin is useful for example in the manufacture of laminates, mineral wool insulation and wood products such as plywood, oriented strandboard (OSB), laminated veneer lumber (LVL), medium density fiberboards (MDF), high density fiberboards (HDF), parquet flooring, curved plywood, veneered particleboards, veneered MDF or particle boards, laminates or mineral wool insulation.

Claims (15)

1. A method for preparing a bonding resin comprising:

mixing lignin in solid form or in the form of a dispersion in water with:

one or more ethers selected from a group consisting of: glycerol diglycidyl ether, diglycerol polyglycidyl ether, polyglycerol polyglycidyl ether, glycerol triglycidyl ether, sorbitol polyglycidyl ether, alkoxylated glycerol polyglycidyl ether, trimethylolpropane triglycidyl ether, trimethylolpropane diglycidyl ether, polyoxypropylene glycol diglycidylether, polyoxypropylene glycol triglycidyl ether, diglycidylether of cyclohexane dimethanol, resorcinol diglycidyl ether, isosorbide diglycidyl ether, pentaerythritol tetraglycidyl ether, ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether having 2-9 ethylene glycol units, propylene glycol diglycidyl ether having 1-5 propylene glycol units, hexahydrophtalic acid diglycidylester and/or diglycidyl ether of terminal diol having a linear carbon chain of 3-6 carbon atoms, or a crosslinker selected from diglycidyl-, triglycidyl-or polyglycidyl-ether of a carbohydrate, diglycidyl-, triglycidyl-or polyglycidyl-ester of a carbohydrate, diglycidyl-ether or diglycidyl ester of salicylic acid, vanillic acid, or 4-hydroxybenzoic acid, an epoxidized or glycidyl substituted plant-based phenolic compound or epoxidized plant-based oil, tris (4-hydroxyphenyl) methane triglycidyl ether, N,N-bis(2,3-epoxypropyl) aniline, p-(2,3-epoxypropoxy-N,N-bis (2,3-epoxypropyl) aniline, diglycidyl ether of bis-hydroxymethylfuran, and a compound having functional groups selected from diglycidyl amide, triglycidyl amide, polyglycidyl amide, diglycidyl ester, triglycidyl ester, polyglycidyl ester, diglycidyl azide, triglycidyl azide, polyglycidyl azide, diglycidyl methacrylate, triglycidyl methacrylate and polyglycidyl methacrylate, wherein the lignin has not been chemically modified, and,

addition of a basic solution after the mixing, the basic solution having a pH in a range of from 10 to 14.

2. The method according to claim 1 , wherein the lignin is in solid form and is mixed with one or more ethers selected from a group consisting of: glycerol diglycidyl ether, diglycerol polyglycidyl ether, polyglycerol polyglycidyl ether, glycerol triglycidyl ether, sorbitol polyglycidyl ether, alkoxylated glycerol polyglycidyl ether, trimethylolpropane triglycidyl ether, trimethylolpropane diglycidyl ether, polyoxypropylene glycol diglycidylether, polyoxypropylene glycol triglycidyl ether, diglycidylether of cyclohexane dimethanol, resorcinol diglycidyl ether, isosorbide diglycidyl ether, pentaerythritol tetraglycidyl ether, ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether having 2-9 ethylene glycol units, propylene glycol diglycidyl ether having 1-5 propylene glycol units, hexahydrophtalic acid diglycidylester and/or diglycidyl ether of terminal diol having a linear carbon chain of 3-6 carbon atoms.

3. The method according to claim 1 , wherein the ether comprises polyglycerol polyglycidyl ether.

4. The method according to claim 1 , wherein the lignin is further mixed with an additive, and wherein the additive comprises a solvent.

5. The method according to claim 1 , wherein a weight ratio between the lignin, calculated on a basis of dry lignin, and a total amount of glycerol diglycidyl ether, or ethylene glycol diglycidyl ether, or both is from 1:10 to 10:1.

6. The method according to claim 1 , wherein the lignin is further mixed with an additive, and wherein the additive is selected from a group consisting of: urea, tannin, a surfactant, a dispersing agent, a filler, and a solvent.

7. The method according to claim 6 , wherein the additive is a solvent comprising glycerol, ethylene glycol, polyethylene glycol, propylene glycol, polypropylene glycol, sorbitol, any terminal diol having a linear carbon chain of 3-6 carbon atoms, or combinations thereof.

8. The method according to claim 1 , wherein the lignin is further mixed with an additive.

9. A method for preparing a bonding resin comprising:

mixing lignin in solid form or in the form of a dispersion in water with one or more ethers selected from a group consisting of: glycerol diglycidyl ether, diglycerol polyglycidyl ether, polyglycerol polyglycidyl ether, glycerol triglycidyl ether, sorbitol polyglycidyl ether, alkoxylated glycerol polyglycidyl ether, trimethylolpropane triglycidyl ether, trimethylolpropane diglycidyl ether, polyoxypropylene glycol diglycidylether, polyoxypropylene glycol triglycidyl ether, diglycidylether of cyclohexane dimethanol, resorcinol diglycidyl ether, isosorbide diglycidyl ether, pentaerythritol tetraglycidyl ether, ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether having 2-9 ethylene glycol units, propylene glycol diglycidyl ether having 1-5 propylene glycol units, hexahydrophtalic acid diglycidylester and/or diglycidyl ether of terminal diol having a linear carbon chain of 3-6 carbon atoms,

wherein the lignin is modified by any method where lignin hydroxyl content or amine content or thiol content is increased and,

addition of a basic solution after the mixing, the basic solution having a pH in a range of from 10 to 14.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2022
From: ZAFAR, ASHAR; EKSTRÖM, JESPER
To: STORA ENSO OYJ
Reel/Frame 058595/0854 →
Priority Claims (1)
SE 1950773-0 · Jun 24, 2019 · national
Continuity (1)
Related Publication 20220243105A1 · Aug 4, 2022
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