Formaldehyde-free binder compositions and methods of making the binders under controlled acidic conditions

Patent metadata

Field	Value
Publication number	US-10988412-B2
Application number	US-201715590544-A
Country	US
Kind code	B2
Filing date	May 9, 2017
Priority date	Aug 11, 2009
Publication date	Apr 27, 2021
Grant date	Apr 27, 2021

Abstract

Formaldehyde-free binder compositions are described that include an aldehyde or ketone, a reaction product between a polyamine and an organic anhydride, and an acidic compound. The acidic compound may be an organic acid, an acidic catalyst, or both. The acidic compound is supplied in quantities that lower the pH of the binder composition to about 5 or less. The binder compositions may be used in methods of binding fiberglass and the resulting fiberglass products have an improved tensile strength due to the addition of the acidic compound.

First claim

What is claimed is:

1. A method of making a fiberglass product, the method comprising:
combining a binder composition and glass fibers, wherein the binder composition includes:
an aldehyde or ketone,
an amino-amide compound that consists of a reaction product of a diamine and a carbonyl compound, wherein the diamine is selected from the group consisting of 1,2-ethylenediamine, 1,3-propanediamine, 1,4-butanediamine, 1,5-pentadiamine, and 1,6-hexanediamine, and
a catalyst for catalyzing a reaction between (i) the aldehyde or ketone and (ii) the amino-amide compound;

forming the combination of the binder composition and the glass fibers into an uncured fiberglass mat or batt; and
heating the uncured fiberglass mat or batt into the fiberglass product.

2. The method of claim 1 , wherein the aldehyde or ketone comprises a reducing sugar.

3. The method of claim 2 , wherein the reducing sugar comprises dextrose.

4. The method of claim 1 , wherein the amino-amide compound is an amino-amide oligomer.

5. The method of claim 1 , wherein the carbonyl compound comprises at least one of an organic acid anhydride, a carboxylic acid, an organic ester, or a salt thereof.

6. The method of claim 5 , wherein the carboxylic acid comprises at least one of maleic acid, fumaric acid, succinic acid, glutaric acid, phthalic acid, or tetrahydrophthaic acid.

7. The method of claim 5 , wherein the organic acid anhydride comprises at least one of maleic anhydride, succinic anhydride, glutaric anhydride, phthalic anhydride, or tetrahydrophthaic anhydride.

8. The method of claim 1 , wherein the carbonyl compound comprises an ammonium salt of a carboxylic acid or organic acid anhydride.

9. The method of claim 1 , wherein the catalyst is an acidic compound that sets a pH for the binder composition to 5 or less.

10. The method of claim 9 , wherein the acidic compound comprises an organic acid or an inorganic acid.

11. The method of claim 10 , wherein the organic acid comprises a polycarboxylic acid.

12. The method of claim 11 , wherein the polycarboxylic acid comprises citric acid.

13. The method of claim 1 , wherein the binder composition is combined with the glass fibers before they are collected and formed into the uncured fiberglass mat or batt.

14. The method of claim 1 , wherein the uncured fiberglass mat or batt is heated at 100° C. to 300° C.

15. The method of claim 1 , wherein the fiberglass product comprises fiberglass insulation.

16. A method of making a fiberglass product, the method comprising:
combining a binder composition and glass fibers, wherein the binder composition includes:
an aldehyde or ketone, and
an amino-amide compound comprising a reaction product of a diamine and a carbonyl compound, wherein the diamine is selected from the group consisting of 1,2-ethylenediamine, 1,3-propanediamine, 1,4-butanediamine, 1,5-pentadiamine, and 1,6-hexanediamine,

forming the combination of the binder composition and the glass fibers into an uncured fiberglass mat or batt; and
heating the uncured fiberglass mat or batt at a temperature of 200° C. to 300° C. for 20 minutes or more to form the fiberglass product.

17. The method of claim 16 , wherein the aldehyde or ketone comprises a reducing sugar.

18. The method of claim 17 , wherein the reducing sugar comprises dextrose.

19. The method of claim 17 , wherein the acidic compound comprises a polycarboxylic acid.

20. The method of claim 19 , wherein the polycarboxylic acid comprises citric acid.

21. The method of claim 16 , wherein the amino-amide compound is an amino-amide oligomer.

22. The method of claim 16 , wherein the carbonyl compound comprises at least one of an organic acid anhydride, a carboxylic acid, an organic ester, or a salt thereof.

23. The method of claim 22 , wherein the carboxylic acid comprises at least one of maleic acid, fumaric acid, succinic acid, glutaric acid, phthalic acid, or tetrahydrophthaic acid.

24. The method of claim 22 , wherein the organic acid anhydride comprises at least one of maleic anhydride, succinic anhydride, glutaric anhydride, phthalic anhydride, or tetrahydrophthaic anhydride.

25. The method of claim 16 , wherein the binder composition further comprises a catalyst for catalyzing a reaction between (i) the aldehyde or ketone and (ii) the amino-amide compound.

26. The method of claim 25 , wherein the catalyst is an acidic compound that sets a pH for the binder composition to 5 or less.

Assignees

• Johns Manville

Inventors

• Alavi Kiarash
• Lester Uranchimeg
• Asrar Jawed

Classifications

• C03C25/321 Primary

  Starch; Starch derivatives · CPC title

• C08K7/14

  Glass · CPC title

• C03C25/32 Primary

  obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds · CPC title

• C08G12/22

  with carboxylic acid amides (reaction of polyamides with aldehydes C08G69/50) · CPC title

• D04H1/587

  characterised by the bonding agents used · CPC title