Glycidyl esters vinyl acetate

Several ester monomers have also been studied. In methanol solution, methyl acrylate (16,21), ethyl acrylate (21,54), 2-ethyl hexyl acrylate (55), allyl acrylate (44), glycidyl acrylate (56,57) usually in methanol solution, have been extensively studied. Methyl methacrylate (19, 21, 28, 30, 36, 39, 58) in diversified media composition, has been successfully grafted on polyamides. Vinyl acetate is reported also for grafting on polyamide backbone (19, 28, 35, 58), as well as n-butyl maleate in methanol solution (55). Diallyl maleate as cross-linking agent for polyamide chains is reported (44). Other less usual ester monomers have been mentioned in the literature to form grafts (41,59,60). 

Terpolymers made from two different olefins and CO are known. They were first described in Brubaker s initial patent and involved the free radical initiated terpolymerization of CO and C2H with another olefin such as propylene, isobutylene, butadiene, vinyl acetate, diethyl maleate or tetrafluoroethylene More recently, in another patent, Hammer has described the free radical initiated terpolymerization of CO and C2H with vinyl esters, vinyl ethers or methyl methacrylate 26Reaction temperatures of 180-200 °C and a combined pressure of 186 MPa were employed. Typically a CO QH4 olefin molar ratio of 10 65 25 was observed in the terpolymers. In other patents, Hammer 27,28) has described the formation of copolymers with pendant epoxy groups by the free radical initiated polymerization of CO, QH4, vinyl acetate and glycidyl methacrylate. Reaction conditions similar to those stated above were employed, and a typical CO C2H vinyl acetate glycidyl methacrylate molar ratio of 10 65 20 5 was observed in the product polymer. 

Ally Acetate can be a starting material for polymers as a comonomer, for glycidyl acetate as a component of epoxy resins, for glycerol, for allyl alcohol by hydrolysis, and for the synthesis of allyl esters of higher acids or other compounds by transesterification or transallylation. Processes for the commercial production of allyl acetate have been developed by Bayer and Hoechst [60], and some Japanese companies. Such processes work in the gas-phase under similar conditions to those used in vinyl acetate manufacture and are currently operated by Showa Denko and Daicel [61]. 

Neodecanoic acid, ethenyl ester, polymer with 2-butenoic acid and ethenyl acetate. See VA/crotonates/vinyl neodecanoate copolymer Neodecanoic acid glycidyl ester. See Glycidyl neodecanoate... 

Styrene/a-methyl styrene Styrene/(halogenated styrene) Styrene/(halogenated styrene) a-methylstyrene/acrylonitrile a-methylstyrene/methacrylonitrile Butadiene/acrylonitrile Butadiene/acrylonitrile (methyl methacrylate)/(alkyl methacrylates) (methyl methacrylate)/esters (glycidyl methacrylate)/(ethyl acrylate) (ethylene terephthalate)/oxybenzoate (ethyl acrylate)/(4-vinyl pyridine) Ethylene/(vinyl acetate)... 

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