Dual cure composite resins containing uretdione and unsaturated sites
US-9175117-B2 · Nov 3, 2015 · US
US9580527B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9580527-B2 |
| Application number | US-201514926656-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 29, 2015 |
| Priority date | Mar 15, 2013 |
| Publication date | Feb 28, 2017 |
| Grant date | Feb 28, 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.
The present invention provides a dual-cure composition containing multifunctional polyols, uretdiones, peroxide curable monomers containing unsaturation and crosslinking agents. The dual-cure composition may be used to form a high modulus material useful as the matrix in a prepreg material and in composites. The present invention also relates to methods for the production of the dual-cure composition, prepreg materials comprising the dual-cure composition and a fibrous support, and composites made from the prepreg material.
Opening claim text (preview).
What is claimed is: 1. A dual-cure composition containing: (A) a multifunctional polyol; (B) a curing agent containing uretdione groups; (C) a low viscosity unsaturated reactive diluent; (D) at least one reactively activatable catalyst; and (E) a thermal crosslinking initiator; wherein the composition cures at 80-130° C. 2. The dual-cure composition of claim 1 , wherein the heat of polymerization of the dual-cure composition is less than 170 J/g. 3. The dual-cure composition of claim 1 , wherein the heat of polymerization of the dual-cure composition is less than 130 J/g. 4. The dual-cure composition of claim 1 , further comprising an epoxy functional molecule. 5. The dual-cure composition of claim 1 , further comprising a free radical scavenger. 6. The dual-cure composition of claim 5 , wherein the free radical scavenger is a nitroxide compound. 7. The dual-cure composition of claim 1 , further comprising an antifoaming agent. 8. The dual-cure composition of claim 1 , wherein said component (A) is a free radically reactive polyol monomer selected from the group consisting of a vinyl ether, an allyl ether, an acrylate, a methacrylate, a urethane acrylate, allophanate acrylate, epoxy acrylate, alone or in a mixture. 9. The dual-cure composition of claim 1 , wherein said component (A) is a non-free radically reactive polyol oligomer selected from the group consisting of an ether, an ester, an epoxy, an alkyd, a urethane, alone or in a mixture. 10. The dual-cure composition of claim 1 , wherein said component (B) is selected from the group consisting of isophorone diisocyanate (IPDI) containing uretdione groups, hexamethylene diisocyanate (HDI) containing uretdione groups, diisocyanatodicyclohexylmethane (H 12 MDI) containing uretdione groups, diphenylmethane 4,4′-diisocyanate (MDI) containing uretdione groups, diphenylmethane 2,4′-diisocyanate (MDI) containing uretdione groups, 2,4-toluene diisocyanate (TDI) containing uretdione groups and 2,6-toluene diisocyanate (TDI) containing, uretdione groups. 11. The dual-cure composition of claim 1 , wherein said component (C) is a peroxide curable monomer selected from the group consisting of an acrylate, a methacrylate, a urethane acrylate, a urethane methacrylate, a polyester acrylate, a polyester methacrylate, a polyether acrylate, a polyether methacrylate, an allyl ether acrylate, an allyl ether methacrylate, an ester acrylate, an ester methacrylate, an allophonate urethane acrylate, an allophonate urethane methacrylate, an epoxy acrylate, an epoxy methacrylate, a vinyl ether, alone or in a mixture. 12. The dual-cure composition of claim 1 , wherein said component (D) is a lewis acid comprising at least one metallo-organic catalyst of the general formula: R n MeX y in which Me is a metal, R is an alkyl residue, X is a carboxylate residue, an alcoholate residue, or an acetylacetonate residue, n=0 or 2, and y=2 or 3. 13. The dual-cure composition of claim 1 , wherein said component (D) is Zn acetylacetonate. 14. The dual-cure composition of claim 1 , wherein said component (E) consists essentially of a peroxide or hydro-peroxide compound. 15. A dual-cure composition containing: (A) a free radically reactive polyol monomer selected from the group consisting of a vinyl ether, an allyl ether, an acrylate, a methacrylate, a urethane acrylate, alone or in a mixture: (B) a curing agent selected from the group consisting of isophorone diisocyanate (IPDI) containing uretdione groups, hexamethylene diisocyanate (HDI) containing uretdione groups, diisocyanatodicyclohexylmethane (H 12 MDI) containing uretdione groups, diphenylmethane 4,4′-diisocyanate (MDI) containing uretdione groups, diphenylmethane 2,4′-diisocyanate (MDI) containing uretdione groups, and 2,4-toluene diisocyanate (TDI) containing uretdione groups, and 2,6-toluene diisocyanate (TDI) containing uretdione groups; (C) a low viscosity unsaturated reactive diluent selected from the group consisting of a (meth)acrylate, a urethane (meth)acrylate, a polyester (meth)acrylate, a polyether (meth)acrylate, an allyl ether (meth)acrylate, an ester (meth)acrylate, an allophonate urethane (meth)acrylate, an epoxy (meth)acrylate, a vinyl ether, alone or in a mixture; (D) at least one reactively activatable catalyst comprising a lewis acid containing at least one metallo-organic catalyst of the general formula: R n MeX y in winch Me is a metal, R is an alkyl residue, X is a carboxylate residue, an alcoholate residue, or an acetylacetonate residue, n=0 or 2, and y=2 or 3; (E) a thermal crosslinking initiator activatable by actinic radiation; (F) an acid scavenger; and (G) acrylate co-catalyst, wherein the composition cures at 80-130° C.
Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain (of polyester-amides C08L77/12; of polyester-imides C08L79/08); Compositions of derivatives of such polymers · CPC title
Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen (of cyclic esters of polyfunctional acids C08L31/00; of cyclic anhydrides of unsaturated acids C08L35/00); Compositions of derivatives of such polymers · CPC title
Silicon-containing compounds · CPC title
Esters · CPC title
containing aromatic groups or benzoquinone groups · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.