Use of bonding resin

US12077682B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12077682-B2
Application numberUS-202017610856-A
CountryUS
Kind codeB2
Filing dateMay 13, 2020
Priority dateMay 15, 2019
Publication dateSep 3, 2024
Grant dateSep 3, 2024

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention relates to the use of a bonding resin prepared by providing an aqueous solution comprising at least one biobased product selected from tannin, starch, soy protein, glycerol, chitin, pectin, dextrose or other carbohydrates, or a mixture thereof and mixing the aqueous solution with one or more of certain crosslinkers such as ethers, and optionally one or more additives. The bonding resin is used in the manufacture of laminates, mineral wool insulation or wood products, such as engineered wood products, such as plywood, oriented strandboard (OSB), laminated veneer lumber (LVL), medium density fiberboards (MDF), high density fiberboards (HDF) or particle boards. Preferably, the bonding resin does not comprise lignin.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method of preparing a bonding resin by: providing an aqueous solution comprising at least one biobased product selected from a group consisting of tannin, starch, soy protein, glycerol, chitin, pectin, dextrose or other carbohydrates, and mixtures thereof; mixing the aqueous solution with one or more of glycerol diglycidyl ether, diglycerol polyglycidyl ether, polyglycerol diglycidyl 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, 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 crosslinker 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. 2. The method of claim 1 , wherein the aqueous solution is mixed with one or more of glycerol diglycidyl ether, diglycerol polyglycidyl ether, polyglycerol diglycidyl 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, and/or diglycidyl ether of terminal diol having a linear carbon chain of 3-6 carbon atoms. 3. The method according to claim 2 , wherein the aqueous solution is mixed with polyglycerol polyglycidyl ether. 4. The method according to claim 1 , wherein the aqueous solution comprising at least one biobased product is an alkali solution. 5. The method according to claim 1 , wherein a weight ratio between the at least one biobased product, calculated on a basis of dry biobased product, and a total amount of ether is from 1:10 to 10:1. 6. The method according to claim 1 , wherein the aqueous solution is further mixed with urea, or a solvent, or both. 7. The method according to claim 6 , wherein the solvent comprises glycerol, ethylene glycol, polyethylene glycol, propylene glycol, polypropylene glycol, sorbitol, any terminal diol having a linear carbon chain of 3-6 carbon atoms, or mixtures thereof. 8. The method according to claim 1 , wherein the biobased product is selected from a group consisting of tannin, starch, soy protein, glycerol, chitin, pectin, dextrose, and mixtures thereof. 9. The method according to claim 1 , further comprising: providing the bonding resin to a surface in preparation of a laminate, mineral wool insulation, wood product, oriented strandboard (OSB), laminated veneer lumber (LVL), medium density fiberboards (MDF), high density fiberboards (HDF), particle board, parquet flooring, curved plywood, veneered particleboards, or veneered MDF, and curing the bonding resin to form an adhesive by exposing the surface to pressure. 10. The method according to claim 1 , wherein the aqueous solution is further mixed with one or more additives. 11. The method of claim 9 , wherein the bonding resin is cured to form an adhesive by exposing the surface to pressure and heating. 12. A method for manufacturing a wood product comprising: preparing a bonding resin by providing an aqueous solution comprising at least one biobased product selected from a group consisting of tannin, starch, soy protein, glycerol, chitin, pectin, dextrose or other carbohydrates, and mixtures thereof, and mixing the aqueous solution with one or more of glycerol diglycidyl ether, polyglycerol diglycidyl 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, 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 crosslinker 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; providing the bonding resin to a surface in preparation of the wood product, and curing the bonding resin to form an adhesive by exposing the surface to pressure. 13. The method according to claim 12 , wherein the aqueous solution is further mixed with one or more additives. 14. The method according to claim 12 , wherein the bonding resin is cured to form an adhesive by exposing the surface to pressure and heating.

Assignees

Inventors

Classifications

  • Adhesives based on proteins; Adhesives based on derivatives thereof · CPC title

  • C09J163/00Primary

    Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins · CPC title

  • Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof · CPC title

  • C09J105/06Primary

    Pectin; Derivatives thereof · CPC title

  • of wood (B32B21/13 takes precedence) · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US12077682B2 cover?
The present invention relates to the use of a bonding resin prepared by providing an aqueous solution comprising at least one biobased product selected from tannin, starch, soy protein, glycerol, chitin, pectin, dextrose or other carbohydrates, or a mixture thereof and mixing the aqueous solution with one or more of certain crosslinkers such as ethers, and optionally one or more additives. The …
Who is the assignee on this patent?
Stora Enso Oyj
What technology area does this patent fall under?
Primary CPC classification C09J163/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 03 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).