US2013203894A1PendingUtilityA1
Cycloaliphatic carbonates as reactive diluents in epoxy resins
Est. expiryMar 11, 2030(~3.7 yrs left)· nominal 20-yr term from priority
Inventors:Bruce L. Burton
C08G 59/32F03D 13/10C08G 59/22C08L 63/00C08G 59/50B29K 2063/00C08G 59/5026F05B 2230/30C08J 5/00C08G 59/226C08G 59/68B29C 45/0001C08G 65/2624B29K 2105/0014B29K 2105/0047C08G 59/245B29L 2031/085C08G 59/502C08J 2363/02B29C 45/72Y02E10/72C08G 2120/00
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Claims
Abstract
Embodiments of the present invention disclose a method for limiting peak exotherm temperatures in epoxy systems comprising the step of: combining an amine hardener, an epoxy and a diluent to form an epoxy system, wherein the diluent is selected from the group consisting of: ethylene carbonate, propylene carbonate, butylene carbonate, delta-valerolactam, delta-valerolactone, gamma valerolactone, butyrolactam, beta butyrolactone, gamma butyrolactone, and combinations thereof.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for limiting peak exotherm temperatures in an epoxy system comprising the step of:
combining an amine hardener, an epoxy, and a diluent to form an epoxy system; wherein the diluent is selected from the group consisting of: ethylene carbonate, propylene carbonate, butylene carbonate, delta-valerolactam, delta-valerolactone, gamma valerolactone, butyrolactam, beta butyrolactone, gamma butyrolactone, and combinations thereof.
2 . The method of claim 1 wherein the diluent is propylene carbonate
3 . The method of claim 1 wherein the diluent is selected from the group consisting of: delta-valerolactam, delta-valerolactone, gamma valerolactone, butyrolactam, beta butyrolactone, gamma butyrolactone, and combinations thereof.
4 . The method of claim 1 wherein the epoxy system is substantially free of an aliphatic glycidyl ether.
5 . The method of claim 4 wherein the aliphatic glycidyl ether comprises a diglycidyl ether of 1,4-butane diol.
6 . The method of claim 1 wherein the amine hardener comprises an aliphatic amine having an amine-hydrogen functionality greater than two amine hydrogens per molecule.
7 . The method of claim 1 wherein the epoxy comprises a multifunctional polyglycidyl ether of dihydric phenol.
8 . The method of claim 1 further comprising the step of heating the epoxy system.
9 . The method of claim 1 further comprising the step of injecting, filling, or infusing the epoxy system into a mold.
10 . The method of claim 9 wherein the mold is a wind blade mold.
11 . The method of claim 1 , wherein the diluent has a weight percent in the epoxy system in the range of from about two percent to about thirty percent.
12 . The method of claim 1 further comprising the step of adding a reactivity agent to the epoxy system.
13 . The method of claim 12 wherein the reactivity agent is selected from the group consisting of: glycerin carbonate, glycerin, N-aminoethyl piperazine, and combinations thereof.
14 . The method of claim 1 wherein the epoxy system further comprises an additive.
15 . The method of claim 14 wherein the additive is selected from the group consisting of: a processing aid, a filler, a stabilizer, an additive, an adjuvant and combinations thereof.
16 . An article of manufacture produced by the method of claim 1 .
17 . The article of manufacture of claim 16 , wherein the article of manufacture comprises a wind blade.
18 . The use of the method of claim 1 to produce a molded epoxy composite article.
19 . The use of the method of claim 16 wherein the epoxy composite article comprises a composite blade used in the generation of electricity.Cited by (0)
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