Two-component composition
US-2015368466-A1 · Dec 24, 2015 · US
US10160826B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10160826-B2 |
| Application number | US-201414763951-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 5, 2014 |
| Priority date | Mar 15, 2013 |
| Publication date | Dec 25, 2018 |
| Grant date | Dec 25, 2018 |
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A hardener composition comprising: a) an isolated adduct comprising a reaction product of i) a polymer with a functionality of at least three, wherein said polymer contains at least one epoxy group; and ii) an amine wherein the isolated adduct is present as an aqueous solution; and b) a capping agent. This hardener can be used with a liquid epoxy resin to form a curable composition.
Opening claim text (preview).
That which claimed is: 1. A hardener composition comprising: a) an aqueous solution of an isolated adduct; b) a capping agent; and c) a modifier consisting of benzyl alcohol; wherein said isolated adduct is a reaction product of: i) an aliphatic polymer with a functionality of at least three and containing at least one epoxy group; and ii) a polyamine; wherein at least one of said capping agent b) and said modifier c) is present in an amount of from 0.05 weight percent to 5 weight percent, based on the total weight of the hardener composition. 2. A hardener composition in accordance with claim 1 wherein said polyamine ii) is selected from the group consisting of ethylenediamine, diethylenetriamine, triethylenetetramine, m-xylylenediamine, methylpentamethylenediamine, 1,3-BAC and combinations thereof. 3. A hardener composition in accordance with claim 1 wherein said capping agent b) is selected from the group consisting of ethylene oxide, propylene oxide, butylene oxide, phenyl glycidyl ether, cresyl glycidyl ether, p.t-butylphenyl glycidyl ether, C12/C14 fatty alcohol glycidyl ether, and formaldehyde. 4. A hardener composition in accordance with claim 1 wherein said aliphatic polymer i) accounts for 30 weight percent to 95 weight percent of the isolated adduct, and said polyamine ii) accounts for 5 weight percent to 70 weight percent of the isolated adduct, based on the total weight of the isolated adduct. 5. A hardener composition in accordance with claim 1 wherein said isolated adduct is present in an amount of from 5 weight percent to 95 weight percent, based on the total weight of the hardener composition. 6. The hardener composition in accordance with claim 1 , wherein said modifier c) is present in an amount of from 0.05 weight percent to 5 weight percent, based on the total weight of the hardener composition. 7. The hardener composition in accordance with claim 1 , wherein said capping agent b) is present in an amount of from 0.05 weight percent to 5 weight percent, based on the total weight of the hardener composition. 8. A curable composition comprising: i) the hardener composition of claim 1 ; and ii) an epoxy resin selected from the group consisting of liquid bisphenol-A diglycidyl ethers, liquid bisphenol-F diglycidyl ethers, liquid epoxy novolacs, solid bisphenol-A epoxy resins, and combinations thereof. 9. A coating prepared from the composition of claim 8 . 10. A primer prepared from the composition of claim 8 . 11. A process for preparing the hardener composition of claim 1 comprising: contacting said aliphatic polymer i) and a molar excess of said polyamine ii) under reaction conditions to form an adduct; distilling excess polyamine to form said isolated adduct; adding water to form said aqueous solution of an isolated adduct a); admixing said aqueous solution of an isolated adduct a) with said capping agent b); and adding said modifier consisting of benzyl alcohol c); wherein at least one of said capping agent b) and said modifier c) is present in an amount of from 0.05 weight percent to 5 weight percent, based on the total weight of the hardener composition. 12. A process in accordance with claim 11 wherein said reaction conditions comprise a reaction temperature in the range of from 60° C. to 140° C.
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