Curable fiberglass binder
US-9365963-B2 · Jun 14, 2016 · US
US9676954B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9676954-B2 |
| Application number | US-201213478765-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 23, 2012 |
| Priority date | Aug 11, 2009 |
| Publication date | Jun 13, 2017 |
| Grant date | Jun 13, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
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.
Opening claim text (preview).
What is claimed is: 1. A formaldehyde-free binder composition comprising: an aldehyde or ketone; a reaction product between a polyamine and an organic anhydride, wherein the reaction product comprises an amino-amide oligomer, the polyamine is selected from the group consisting of ethylene diamine, 1,3-propanediamine, 1,4-butanediamine, 1,5-pentanediamine, 1,6-hexanediamine, α,α′-diaminoxylene, diethylenetriamine, triethylenetetramine, and tetraethylenepentamine, and the amino-amide oligomer and the aldehyde or ketone have a molar ratio from 1:3 to 1:10; and an acidic catalyst to catalyze the reaction between the amino-amide oligomer and the aldehyde or ketone, wherein: the pH of the binder composition is 5 or less, and the amino-amide oligomer is a dimer, trimer, or tetramer. 2. The formaldehyde-free binder composition of claim 1 , wherein the acidic catalyst comprises an ammonium salt of an inorganic acid. 3. The formaldehyde-free binder composition of claim 1 , wherein the acidic catalyst comprises an ammonium salt of sulfuric acid or phosphoric acid. 4. The formaldehyde-free binder composition of claim 1 , wherein the acidic catalyst comprises an ammonium salt of an inorganic acid chosen from mono-ammonium sulfate, di-ammonium sulfate, mono-ammonium phosphate, and di-ammonium phosphate. 5. The formaldehyde-free binder composition of claim 1 , wherein the aldehyde or ketone is a reducing sugar. 6. The formaldehyde-free binder composition of claim 1 , wherein the organic anhydride is one or more anhydrides chosen from maleic anhydride, itaconic anhydride, phthalic anhydride, and tetrahydrophthalic anhydride. 7. The formaldehyde-free binder composition of claim 1 , wherein the binder composition comprises one or more additional compounds chosen from adhesion promoters, oxygen scavengers, moisture repellants, solvents, emulsifiers, pigments, fillers, anti-migration aids, coalescent aids, wetting agents, biocides, plasticizers, organosilanes, anti-foaming agents, colorants, waxes, suspending agents, anti-oxidants, and crosslinking catalysts. 8. The method of claim 1 , wherein the acidic compound and the reaction product are present at a molar ratio of 1:1. 9. The method of claim 1 , wherein the reaction product is the product of a reaction between the polyamine and the organic anhydride at a molar ratio of 1:1. 10. The formaldehyde-free binder composition of claim 1 , wherein the amino-amide oligomer is an amino-amide dimer. 11. The formaldehyde-free binder composition of claim 1 , wherein the amino-amide oligomer is an amino-amide trimer. 12. The formaldehyde-free binder composition of claim 1 , wherein the amino-amide oligomer is an amino-amide tetramer. 13. A fiber-reinforced composite comprising: glass fibers; and a cured binder formed from a binder composition comprising: an aldehyde or ketone, a reaction product between a polyamine and an organic anhydride at a molar ratio of 1:1, wherein the reaction product comprises an amino-amide oligomer, and an acidic catalyst to catalyze the reaction between the amino-amide oligomer and the aldehyde or ketone, wherein: the pH of the binder composition is 5 or less, and the amino-amide oligomer is a dimer, trimer, or tetramer. 14. The fiber-reinforced composite of claim 13 , wherein the fiber-reinforced composite comprises a fiberglass building insulation. 15. A method of binding fiberglass, the method comprising: applying a binder composition to a mat of fiberglass; and curing the binder composition applied to the fiberglass, wherein the binder composition comprises: an aldehyde or ketone, a reaction product between a polyamine and an organic anhydride at a molar ratio of 1:1, wherein the reaction product comprises an amino-amide oligomer, and an acidic catalyst to catalyze the reaction between the amino-amide oligomer and the aldehyde or ketone, wherein: the pH of the binder composition is 5 or less, and the amino-amide oligomer is a dimer, trimer, or tetramer. 16. The method of claim 15 , wherein the amino-amide and the aldehyde or ketone have a molar ratio from 1:3 to 1:10.
characterised by the bonding agents used · CPC title
of aldehydes with acyclic or carbocyclic compounds · CPC title
Starch; Starch derivatives · CPC title
Aldehydes; Ketones · CPC title
Cellulose; Modified cellulose · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.