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Glycidyl esters methyl-methacrylate

The term acrylic apphes to a family of copolymers of monomers that are polymerized by a chain growth mechanism. Most often, the mechanism of polymerization is by free radical initiation. Other mechanisms of polymerization, such as ionic and group transfer polymerization, are possible but will not be discussed in this publication. For a description of other polymerization mechanisms, polymer textbooks are available (5,6). Technically, acrylic monomers are derivatives of acrylic or methacrylic acid. These derivatives are nonfunctional esters (methyl methacrylate, butyl acrylate, etc.), amides (acrylamide), nitrile (acrylonitrile), and esters that contain functional groups (hydroxyethyl acrylate, glycidyl methacrylate, dimethylaminoethyl acrylate). Other monomers that are not acryhc derivatives are often included as components of acryhc resins because they are readily copolymerized with the acryhc derivatives. Styrene is often used in significant quantities in acryhc copolymers. [Pg.132]

Chemical Designations - Synonyms Glycidyl alpha-methyl acrylate Methacrylic acid, 2,3-epoxypropyl ester Chemical Formula CHj=CH(CH3)C00CH2CHCH20. [Pg.192]

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). [Pg.100]

Methacrylic acid glycidyl ester Methacrylic acid hexyl ester Methacrylic acid methyl ester... [Pg.45]

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. [Pg.130]

Synonyms 2,3-Epoxy-1-propanol, methacrylate 2,3-Epoxypropyl methacrylate Glycidyl oc-methyl acrylate GMA Methacrylic acid 2,3-epoxypropyl ester 2-Methyl-2-propenoic acid, oxiranylmethyl ester... [Pg.1132]

Solution polymerization (in ketones, aromatic solvents, esters) is used for lacquer resins, which are physically air drying (copolymers with, e.g., lauryl methacrylate) or stoving (with glycidyl methacrylate or glycol dimethacrylate) lacquers. Water-soluble resins from copolymers of methyl methacrylate with a little methacrylic acid are made in this way, being later neutralized with ammonia. The viscosity improvers (see below) are also synthesized in solution (mineral oil). Suspension-polymtnztA polymer is used for injection-molded, extruded, and dental materials (palate or dental plates, teeth fillings). [Pg.437]

Park et al, reported the synthesis and application of terpolymer bearing cyclic carbonate and cinnamoyl groups. The syntheses of photopolymer with pendant cinnamic ester and cyclic carbonate groups was achieved by the addition reaction of poly(glycidyl methacrylate-co-styrene) with CO2 and then with cinnamoyl chloride. Quaternary ammonium salts showed good catalytic activity for this synthesis. Photochemical reaction experiments revealed that terpolymer with cinnamate and cyclic carbonate groups has good photosensitivity, even in the absence of sensitizer. In order to expand the application of the obtained terpolymer, polymer blends with poly(methyl methacrylate) were also prepared. [Pg.211]

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)... [Pg.106]

The second type of composition is exemplified by a wide variety of acrylate- or methacrylate-ester derivatives of conventional ink vehicles combined with a photoinitiator 1. The reaction product of tung oil fatty acids, glycidyl methacrylate, -benzoquinone, and 2-methyl-imidazole mixed with tung oil and treated with tolylene diisocyanate, combined with benzoin methyl ether (26) 2. Glycerol-linseed oil-isophthalic acid alkyd reacted with isocyanate-containing prepolymer (formed by reaction of tolylene diisocyanate, -henzoquinone, 2-hydroxypropyl acrylate in ethyl acetate solution) using dibutyltin diacetate catalyst, combined with tung oil, synthetic varnish, and benzoin methyl ether (27) 3. Epoxidized... [Pg.177]

The third type of composition is exemplified by acrylate- and methacrylate-ester derivatives of epoxy resins combined with a photoinitiator 1. Epoxy prepolymers (e. g., glycidyl methacrylate-allyl glycidyl ether copolymers or Ciba ECN 1299) combined with a photosensitive aryldiazonium compound (e.g., -nitrobenzenediazonium hexaflourophosphate) (38,39) 2. Epoxy prepolymers (e.g., a diglycidyl ether of disphenol A-(3,4-epoxycyclohexyl)-methyl-3,4-epoxycyclohex-anecarboxylate-alkyl glycidyl ether mixture) combined with a photosensitive aryldiazonium compound (e.g., -chlorobenzenediazonium hexaflourophosphate) and l-methyl-2-pyrrolidone gelation inhibitor (40) ... [Pg.178]

Methyl-2-propenoic acid, oxiranylmethyl ester. See Glycidyl methacrylate... [Pg.1205]

Poly(ethylene-co-glycidyl methacrylate) 2,3-Epoxypropyl mefliacrylate-ethylene copol ner 2606 1-90-5 2-Propenoic acid, 2-methyl-, oxiranylmethyl ester, polymer R (C7H10O3 C2H4)r... [Pg.2287]

Poly(ethylene-ro-methyl acrylate-co-glycidyl methacrylate) 51541-08-3 2-Propenoic acid, 2-methyl-, oxiranylmediyl ester, polymer with ediene and mediyl 2-propenoate R (C7H 10O3 C4H5O2 C2H4)x... [Pg.2288]


See other pages where Glycidyl esters methyl-methacrylate is mentioned: [Pg.347]    [Pg.401]    [Pg.309]    [Pg.2681]    [Pg.64]    [Pg.211]    [Pg.566]    [Pg.177]    [Pg.143]    [Pg.5724]    [Pg.32]    [Pg.101]    [Pg.67]   
See also in sourсe #XX -- [ Pg.104 ]




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Esters methacrylic

Glycidyl esters methacrylate

Methyl methacrylate

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