Carbohydrate polyamine binders and materials made therewith

Patent metadata

Field	Value
Publication number	US-9505883-B2
Application number	US-201414272556-A
Country	US
Kind code	B2
Filing date	May 8, 2014
Priority date	May 7, 2010
Publication date	Nov 29, 2016
Grant date	Nov 29, 2016

Abstract

A binder comprising the products of a carbohydrate reactant and polyamine is disclosed. The binder is useful for consolidating loosely assembled matter, such as fibers. Uncured fibrous products comprising fibers in contact with a carbohydrate reactant and a polyamine are also disclosed. The binder composition may be cured to yield a fibrous product comprising fibers bound by a cross-linked polymer. Further disclosed are methods for binding fibers with the carbohydrate reactant and polyamine based binder.

First claim

The invention claimed is:

1. A method of making a collection of matter bound with a cured, thermoset, polymeric binder comprising:
preparing an aqueous binder solution, said preparing comprising mixing reactants for producing the cured, thermoset, polymeric binder, wherein the reactants consist essentially of a reducing sugar and a primary polyamine H 2 N-Q-NH 2 , wherein Q is alkyl, cycloalkyl, heteroalkyl, or cycloheteroalkyl, each of which is optionally substituted and provided that the primary polyamine does not consist of polyethylenimine;
subsequently disposing the binder solution onto a collection of matter;
subsequently drying the binder solution to form an uncured binder and thermally curing the uncured binder to form the collection of matter bound with the cured, thermoset, polymeric binder.

2. The method of claim 1 , in which the cured, thermoset, polymeric binder is formaldehyde free.

3. The method of claim 1 , in which neither formaldehyde nor phenol is used as a reagent.

4. The method of claim 1 wherein the collection of matter comprises matter selected from the group consisting of glass fibers, mineral fibers, aramid fibers, ceramic fibers, metal fibers, carbon fibers, polyimide fibers, polyester fibers, rayon fibers, cellulosic fibers, wood shavings, sawdust, wood pulp, ground wood, jute, flax, hemp, straw, particulates, coal particulates and sand particulates.

5. The method of claim 1 wherein the collection of matter comprises glass fibers present in the range from 70% to 99% by weight.

6. The method of claim 1 wherein the reducing sugar is selected from the group consisting of dextrose, xylose, fructose, dihydroxyacetone, and mixtures thereof.

7. The method of claim 1 wherein the primary polyamine is selected from the group consisting of a diamine, triamine, tetraamine, and pentamine.

8. The method of claim 1 wherein Q is an alkyl selected from the group consisting of C 2 -C 8 .

9. The method of claim 1 wherein the primary polyamine is selected from the group consisting of 1,6-diaminohexane, 1,5-diamino-2-methylpentane, diethylenetriamine, bis(hexamethylene)triamine, triethylenetetramine, and tetraethylenepentamine.

10. The method of claim 1 wherein a weight ratio of the reducing sugar to the primary polyamine is in the range of 2:1 to 10:1.

11. The method of claim 1 wherein a weight ratio of the reducing sugar to the primary polyamine is in the range of 3:1 to 6:1.

12. The method of claim 1 wherein preparing the binder solution includes adjusting the pH of the binder solution to within the range of 8 to 12.

13. The method of claim 1 wherein the cured binder is substantially water insoluble.

14. The method of claim 1 wherein the polymeric binder strongly absorbs light at 420 nm.

15. The method of claim 1 wherein the binder solution is essentially acid-free.

16. The method of claim 1 wherein the collection of matter and the cured, thermoset, polymeric binder further comprises a material selected from the group consisting of a silicon-containing compound, gamma-aminopropyltriethoxysilane, gamma-glycidoxypropyltrimethoxysilane, aminoethylaminopropyltrimethoxysilane, an aminofunctional oligomeric silane, an aminofunctional oligomeric siloxane and mixtures thereof.

17. The method of claim 1 wherein the collection of matter and the cured, thermoset, polymeric binder further comprises a corrosion inhibitor selected from the group consisting of dedusting oil, monoammonium phosphate, sodium metasilicate pentahydrate, melamine, tin (II)oxalate, and a methylhydrogen silicone fluid emulsion.

18. The method of claim 1 wherein the binder further comprises a non-aqueous moisturizer.

19. The method of claim 1 wherein Q is alkyl, cycloalkyl, heteroalkyl, or cycloheteroalkyl, each of which is optionally substituted by a group selected from the group consisting of amino, hydroxyl, halo, thiol, alkyl, haloalkyl, heteroalkyl, aryl, arylalkyl, arylheteroalkyl, nitro, sulfonic acids and derivatives thereof, and carboxylic acids and derivatives thereof.

20. The method of claim 1 wherein a weight ratio of the reducing sugar to the primary polyamine is in the range of 1:1 to 30:1.

21. The method of claim 1 wherein the binder solution has an alkaline pH.

22. A method of making a composite wood board comprising a collection of matter comprising cellulosic fibers bound with a cured, thermoset, polymeric binder comprising:
preparing an aqueous binder solution, said preparing comprising mixing reactants for producing the cured, thermoset, polymeric binder, wherein the reactants consist essentially of a reducing sugar and a primary polyamine H 2 N-Q-NH 2 , wherein Q is alkyl, cycloalkyl, heteroalkyl, or cycloheteroalkyl, each of which is optionally substituted, provided that the primary polyamine does not consist of polyethylenimine;
subsequently disposing the binder solution onto a collection of matter comprising cellulosic fibers;
subsequently drying the binder solution to form an uncured binder and thermally curing the uncured binder to form the composite wood board bound with the cured, thermoset, polymeric binder;
wherein the composite wood board is selected from the group consisting of: a composite wood board having a modulus of elasticity (MOE) of at least 1800 N/mm 2 ; a composite wood board having a bending strength (MOR) of at least 18 N/mm 2 ; a composite wood board having an internal bond strength (TB) of at least 0.28 N/mm 2 ; a composite wood board which swells less than or equal to 12%, as measured by a change in thickness, after 24 hours in water at 20° C.; a composite wood board having a water absorption after 24 hours in water at 20° C. of less than or equal to 40%; a composite wood board comprising a wax; an orientated strandboard; and a medium density fiberboard.

23. The method of claim 22 wherein the reducing sugar is selected from the group consisting of dextrose, xylose, fructose, dihydroxyacetone, and mixtures thereof.

24. The method of claim 22 wherein Q is alkyl selected from the group consisting of C 2 -C 8 .

25. The method of claim 22 wherein Q is alkyl, cycloalkyl, heteroalkyl, or cycloheteroalkyl, each of which is optionally substituted by a group selected from the group consisting of amino, hydroxyl, halo, thiol, alkyl, haloalkyl, heteroalkyl, aryl, arylalkyl, arylheteroalkyl, nitro, sulfonic acids and derivatives thereof, and carboxylic acids and derivatives thereof.

26. The method of claim 22 wherein the primary polyamine is 1,6-diaminohexane.

27. The method of claim 22 wherein a weight ratio of the reducing sugar to the primary polyamine is in the range of 1:1 to 30:1.

28. The method of claim 22 wherein a weight ratio of the reducing sugar to the primary polyamine is in the range of 2:1 to 10:1.

29. The method of claim 22 wherein a weight ratio of the reducing sugar to the primary polyamine is in the range of 3:1 to 6:1.

30. The method of claim 22 wherein the cellulosic fibers comprise matter selected from the group consisting of wood shavings, sawdust, wood pulp, ground wood, jute, flax, hemp and straw.

31. The method of claim 22 wherein the composite wood board comprises a wax.

32. The method of claim 22 wherein the composite wood board has a modulus of elasticity (MOE) of at least 1800 N/mm 2 .

33. The method of

Assignees

• Knauf Insulation Sprl
• Knauf Insulation Inc

Inventors

• Appley Charles Fitch
• Hampson Carl A
• Mueller Gert R
• Pacorel Benedicte

Classifications

• C08G73/02 Primary

  Polyamines · CPC title

• C08G12/00 Primary

  Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen (aminophenols C08G8/16) · CPC title

• C08G14/00

  Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 · CPC title

• C08G16/00

  Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 (with polynitriles C08G69/38) · CPC title

• C08K7/14

  Glass · CPC title