Oxazolidone ring containing vinyl ester resin and products therefrom

Abstract

A process comprising contacting a) an epoxy resin; b) an adduct comprising at least one oxazolidone ring prepared from a multifunctional epoxy resin and an isocyanate compound; and c) an unsaturated acid to form a vinyl ester, is disclosed.

1 . A process comprising:
 contacting   a) an epoxy resin wherein the epoxy resin is selected from the group consisting of phenol novolac epoxy resins, cresol novolac epoxy resins, bis-phenol A novolac epoxy resins, bisphenol-A novolac epoxy resins, tris-epoxy resins, epoxidized tetrafunctional phenol ethane, epoxidized cyclohexane tetraphenol, dicyclopentadiene epoxy resins, and mixtures thereof;   b) an adduct comprising at least one oxazolidone ring prepared from a multifunctional epoxy resin and an isocyanate compound; and   c) an unsaturated acid   to form a vinyl ester.   
     
     
         2 . (canceled) 
     
     
         3 . The process of  claim 1  wherein the multifunctional epoxy resin is selected from the group consisting of phenol novolac epoxy resins, cresol-novolac epoxy resins, bisphenol-A novolac epoxy resins, epoxidized tetrafunctional phenol ethane, epoxidized cyclohexane tetraphenol, trisepoxy resins, polyfunctional epoxy resins, naphthalene epoxy resins, divinylbenzene, dicyclopentadiene-type epoxy resins, phosphorous containing epoxy resins, multi aromatic epoxy resins, and mixtures thereof. 
     
     
         4 . The process of  claim 1 , wherein the multifunctional epoxy resin comprises an epoxy resin having a functionality of at more than 2.1 and an EEW of from 100 to 300. 
     
     
         5 . The process of  claim 1  wherein the isocyanate compound has an isocyanate group of 2 or more and an IEW of from 100 to 500. 
     
     
         6 . The process of  claim 1  wherein the isocyanate compound is a polymeric isocyanate compound. 
     
     
         7 . The process of  claim 1 , wherein the unsaturated acid is selected from the group consisting of acrylic acid, methacrylic acid, cinnamic acid, crotonic acid, sorbic acid, monomethyl maleate, monobutyl maleate, half esters of unsaturated dibasic acids, and combinations thereof. 
     
     
         8 . The process of  claim 1  wherein the adduct further comprises a catalyst. 
     
     
         9 . The process of  claim 8  wherein the catalyst is selected from the group consisting of a phosphonium compound, an ammonium compound, chromium salts, amino compounds and combinations thereof. 
     
     
         10 . The process of  claim 1  wherein the multifunctional epoxy resin is selected from the group consisting of phenol novolac epoxy resins, cresol-novolac epoxy resins, polyfunctional epoxy resins, naphthalene epoxy resins, dicyclopentadiene-type epoxy resins, phosphorous containing epoxy resins, multi-aromatic epoxy resins and combinations thereof. 
     
     
         11 . The process of  claim 1 , wherein the adduct is present in a range of from about 0.1 weight percent to about 100 weight percent, and the unsaturated acid is present in a range of from about 1 weight percent to about 60 weight percent. 
     
     
         12 . The vinyl ester formed by the process of  claim 1 . 
     
     
         13 . The vinyl ester of  claim 12 , represented by the formula 
       
         
           
           
               
               
           
         
       
       wherein 
       R 1  is selected from the group consisting of a phenyl ring structure, a polymeric phenyl ring structure and derivatives thereof; 
       R 2  is selected from the group consisting of a phenoxy ring structure, a polymeric phenoxy ring structure and derivatives thereof; 
       R is selected from the group consisting of a hydrogen group, an alkyl group, an alkoxy group, a phenyl ring structure, a polymeric phenyl ring structure derivatives of phenyl ring structures, derivatives of polymeric phenyl ring structures, a phenoxy ring structure, a polymeric phenoxy ring structure derivatives of phenoxy ring structures, and derivatives of polymeric phenoxy ring structures; 
       x is an integer between 0 and 5; 
       y is an integer of at least 1; and 
       z is an integer between 0 and 5. 
     
     
         14 . The process of  claim 1  further comprising:
 d) contacting the vinyl ester with a vinyl monomer. 
 
     
     
         15 . The process of  claim 14  wherein the vinyl monomer is selected from the group consisting of styrene, ring-chlorinated styrenes, alkylated styrenes, alkenylated styrenes, vinyl esters of carboxylic acids with 2-6 carbon atoms per molecule, acrylic and methacrylic acid esters without functional groups, allyl compounds and combinations thereof.