US2016130464A1PendingUtilityA1
Modified epoxy resin composition used in high solids coating
Est. expiryMar 20, 2032(~5.7 yrs left)· nominal 20-yr term from priority
C08G 59/245C08G 59/223C08L 63/00C09D 163/00
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Claims
Abstract
This invention relates to a cardanol modified epoxy resin composition, especially, relates to a cardanol and/or dihydric phenol modified epoxy resin composition, a process making thereof and its application in low VOC high solids coating.
Claims
exact text as granted — not AI-modified1 . A process for preparing the epoxy resin composition, the epoxy resin composition comprises the following resins based on the total weight of the epoxy resin composition,
i. from 10% to 75% by weight of a liquid epoxy resin of formula (I):
wherein n is 0 or 1; each R is independently H or —CH 3 ; and R 1 is —C 15 H 25 , —C 15 H 27 , or —C 15 H 29 ;
ii. from 10% to 75% by weight of a compound of formula (V):
wherein n is 0 or 1; each R is independently H or —CH 3 ; and R 1 is —C 15 H 25 , —C 15 H 27 , or —C 15 H 29 ; and
iii. from 10% to 70% by weight of a compound of formula (VI):
wherein x is 1 or 2; each n is independently 0 or 1; each R is independently H or —CH 3 ; and R 11 by formula (VII):
wherein R 2 is independently H or a C 1 -C 15 alkyl or alkenyl group;
the method comprises admixing a liquid epoxy resin of formula (I) and a cardanol moiety.
2 . The process of claim 1 , wherein the liquid epoxy resin of formula (I) comprises 60% to 95% by weight based on the total weight of the mixture of a diglycidyl ether of a bisphenol.
3 . The process of claim 2 , wherein the diglycidylether of bisphenol is chosen from a group of the diglycidylether Bisphenol A, the diglycidylether Bisphenol F, and combinations thereof.
4 . The process of claim 2 , wherein the liquid epoxy resin of formula (I) is in liquid state without adding any solvent.
5 . The process of claim 1 , wherein the epoxy resin composition is optionally reacted with a dihydric phenol.
6 . The process of claim 4 , wherein the dihydric alcohol is chosen from a group of cardanol, bisphenol A, bisphenol F, resorcinol, or combinations thereof.
7 . The process of claim 1 , wherein a catalyst is optionally added.
8 . The process of claim 7 , wherein the catalyst is selected from a group comprising a basic inorganic reagent, a phosphine, a quaternary ammonium compound, phosphonium reagents, tertiary amines, and combinations thereof.
9 . The process of claim 8 , wherein the catalyst is triphenylphosphonium acetate.
10 . The process of claim 1 , wherein the process is conducted in the absence of solvent.
11 . The process of claim 1 , wherein the temperature ranges from 20° C. to 260° C.Cited by (0)
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