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Glycidyl acetates

Similarly, 4-acetoxymethyl-l,3,2-dioxathiolane A-oxide was obtained in the reaction of glycidyl acetate with sulfur dioxide <1996MM826>. [Pg.183]

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]. [Pg.1330]

Oxiranedimethanol, monopropanoate Oxiranemethanol, acetate glycidyl acetate 3553, 4249 2917a ... [Pg.422]

Glycidyl acetal derivatives, that is, C3 chiral building blocks bearing one stereo-genic center and two different and chemically differentiable fimctions (such as protected aldehyde and epoxide) located on a short carbon skeleton, are of particular... [Pg.208]

The 2-azo derivative (322), when heated with butyl glycidyl ether in acetic acid, reacts through the ring nitrogen (Scheme 186) (585). [Pg.108]

Gun Propellents. Low sensitivity gun propeUants, often referred to as LOVA (low vulnerabUity ammunition), use RDX or HMX as the principal energy components, and desensitizing binders such as ceUulose acetate butyrate or thermoplastic elastomers (TPE) including poly acetal—polyurethane block copolymers, polystyrene—polyacrjiate copolymers, and glycidyl azide polymers (GAP) to provide the required mechanical... [Pg.40]

Property AHyl chloride AHyl acetate AHyl methacrylate AHyl glycidyl ether AGE AHyl amine dimethyl ally amine dmaa "... [Pg.76]

The (9-cresol novolaks of commercial significance possess degrees of polymerization, n, of 1.7—4.4 and the epoxide functionaUty of the resultant glycidylated resins varies from 2.7 to 5.4. Softening points (Durran s) of the products are 35—99°C. The glycidylated phenol and o-cresol—novolak resins are soluble in ketones, 2-ethoxyethyl acetate, and toluene solvents. The commercial epoxy novolak products possess a residual hydrolyzable chlorine content of <0.15 wt% and a total chlorine content of ca 0.6 wt % (Table 2). [Pg.363]

Isoamyl acetate Isoamyl alcohol Isobutyl acetate Isobutyl alcohol Isophorone Isopropyl acetate Isopropyl alcohol Isopropylamine Isopropyl ether Isopropyl glycidyl ether Kaolin Ketene... [Pg.379]

Another example of interest with regard to the reaction mechanism is the analysis of epoxy groups. Durbetaki60 titrated a-epoxy compounds with HBr (cf., p. 260) in glacial acetic acid with crystal violet as indicator, but the method was slow for glycidyl esters, CH2—CHCH2OOCR. As it concerns a two-step... [Pg.303]

A Japanese patent72) claims the synthesis of thermally stable copolymers by free-radical terpolymerization of dialkylstannyl dimethacrylates, glycidyl methacrylate and vinyl monomers (vinyl chloride, styrene, vinyl acetate, etc.). The products contain 0.5 to 30% tin and 0.05 to 7 % epoxide oxygen. [Pg.120]

Photoacid generator. D1 (4 wt%) was mixed with poly(glycidyl methacrylate) (PGMA) (20 wt%) in ethyl cellosolve acetate. The mixture was spin-coated on a silicon wafer and baked at 80V for 1 minute. Exposure was performed with a 600-W Xe-Hg lamp in conjunction with a UVD2 filter. The resist was developed in a mixture of methyl ethyl ketone to ethanol (7/1 w/w). [Pg.321]

Steele, W.V., Chirico, R.D., Cowell, A.B., Knipmeyer, S.E., and Nguyen, A. Thermodynamic properties and ideal-gas enthalpies of formation for 2-aminoisobutyric acid (2-methylalanine), acetic acid, ( -5-ethylidene-2-norbornene, mesityl oxide (4-methyl-3-penten-2-one), 4-methylpent-l-ene, 2,2 -bis(phenylthio)propane, and glycidyl phenyl ether (1,2-epoxy-3-phenox3q>ropane), / Chem. Eng. Data, 42(6) 1053-1066, 1997. [Pg.1728]

Figure 42. A plot of proton beam vs electron beam sensitivity for several resist systems. COP is a copolymer of glycidyl methacrylate and ethyl acrylate, PVC is poly (vinylcinnamate), PCS is poly (chlorostyrene), PTBMA is polyO-butyl methacrylate), PVA is poly (vinyl acetate), PMMA is poly (methyl methacrylate). (Reproduced with permission from Ref. 57 J... Figure 42. A plot of proton beam vs electron beam sensitivity for several resist systems. COP is a copolymer of glycidyl methacrylate and ethyl acrylate, PVC is poly (vinylcinnamate), PCS is poly (chlorostyrene), PTBMA is polyO-butyl methacrylate), PVA is poly (vinyl acetate), PMMA is poly (methyl methacrylate). (Reproduced with permission from Ref. 57 J...
Butoxy ethanol sec-Butyl acetate t-Butyl acetate n-Butyl acetate sec-Butyl alcohol t-Butyl alcohol n-Butyl alcohol n-Butyl glycidyl ether p-tert-Butyl toluene... [Pg.185]

Pentanone Petroleum distillates Phenyl ether vapor Phenyl glycidyl ether n-Propyl acetate Propyl alcohol n-Propyl nitrate Propylene dichloride Propylene oxide Pyridine... [Pg.185]

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]

Matejka et al. 51> studied the reaction of phenyl glycidyl ether (PGE) with acetic or benzoic acid anhydride in the presence of benzyldimethylamine and also with benzoic acid as a co-catalyst. They found that the tert-amine is bound irreversibly through the formation of a quartemary ammonium salt as shown below. [Pg.122]

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]


See other pages where Glycidyl acetates is mentioned: [Pg.191]    [Pg.602]    [Pg.1692]    [Pg.55]    [Pg.122]    [Pg.209]    [Pg.191]    [Pg.602]    [Pg.1692]    [Pg.55]    [Pg.122]    [Pg.209]    [Pg.66]    [Pg.345]    [Pg.368]    [Pg.762]    [Pg.58]    [Pg.59]    [Pg.2391]    [Pg.865]    [Pg.216]    [Pg.180]    [Pg.310]    [Pg.1481]    [Pg.1489]    [Pg.370]    [Pg.31]    [Pg.174]    [Pg.106]    [Pg.259]    [Pg.12]   
See also in sourсe #XX -- [ Pg.55 ]




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