Epichlorohydrin-ethylene oxide-allyl

Hydrex . See Sodium silicoaluminate Hydridocarbonyltris (triphenylphosphine) rhodium (I). See Tristriphenylphosphine rhodium carbonyl hydride Hydrin C Hydrin C-CG. See Epichlorohydrin/ethylene oxide copolymer Hydrin H. See Epichlorohydrin elastomer Hydrin T, Hydrin T-CG, Hydrin TX-1. See Epichlorohydrin/ethylene oxide/allyl glycidyl ether terpolymer Hydrine . See PEG-2 stearate Hydriodic acid... [Pg.2059]

Poly (epichlorohydrin-co-ethylene oxide-co-allyl glycidyl ether). See Epichlorohydrin/ethylene oxide/allyl glycidyl ether terpolymer... [Pg.3463]

Ethylene/propylene/dicyclopentadiene terpolymer Ethylene-propylene-ethylidene norbornene elastomer, adhesives Epichlorohydrin elastomer Epichlorohydrin/ethylene oxide/allyl glycidyl ether terpolymer Epichlorohydrin/ethylene oxide copolymer Polyisoprene Polyurethane, thermoplastic... [Pg.5142]

Epichlorohydrin/ethylene oxide/allyl glycidyl ether terpolymer elastomer, bladders... [Pg.5142]

Allyl Glycidyl Ether. This ether is used mainly as a raw material for silane coupling agents and epichlorohydrin mbber. Epichlorohydrin mbber is synthesized by polymerizing the epoxy group of epichlorohydrin, ethylene oxide, propylene oxide, and aHyl glycidyl ether, AGE, with an aluminum alkyl catalyst (36). This mbber has high cold-resistance. [Pg.77]

AGE-Gontaining Elastomers. ECH—AGE, poly(epichlorohydrin-fo-allyl glycidyl ether) [24969-09-3] (3), ECH—EO—AGE, poly(epichlorohydrin- (9-ethylene oxide-i (9-allyl glycidyl ether) [26587-37-1] (4), ECH—PO—AGE, and PO—AGE are also amorphous polymers. [Pg.553]

AECO terpolymers of allyl glycidyl ether, ethylene oxide and epichlorohydrin... [Pg.947]

Polyepichlorohydrin and copolymers and terpolymers of epichlorohydrin with ethylene oxide and allyl glycidyl ether are useful elastomers [Body and Kyllinstad, 1986]. [Pg.569]

ELASTOMERS,SYNTHETIC - POLYETHERS] (Vol 8) Poly(epichlorohydrin-co-ethylene oxide-co-allyl glyadyl ether)[26587-37-l... [Pg.781]

The coordination polymerisation and copolymerisation of heterocyclic monomers have been restricted in industry to a much smaller volume than the polymerisation and copolymerisation of hydrocarbon monomers polyether elastomers from epichlorohydrin and ethylene oxide or propylene oxide, and allyl glycidyl ether as the vulcanisable monomeric unit, are produced on a larger scale [4-7],... [Pg.426]

Another commercial application of organoaluminum compounds is as catalysts for the ring-opening polymerization of epoxides to form homopolymers of epichlorohydrin (ECH) and copolymers and terpolymers of ECH, ethylene oxide, propylene oxide, and allyl glycidyl ether.The resulting... [Pg.167]

Key Words Ethylene oxide, Propylene oxide. Epoxybutene, Market, Isoamylene oxide. Cyclohexene oxide. Styrene oxide, Norbornene oxide. Epichlorohydrin, Epoxy resins, Carbamazepine, Terpenes, Limonene, a-Pinene, Fatty acid epoxides, Allyl epoxides, Sharpless epoxidation. Turnover frequency, Space time yield. Hydrogen peroxide, Polyoxometallates, Phase-transfer reagents, Methyltrioxorhenium (MTO), Fluorinated acetone, Alkylmetaborate esters. Alumina, Iminium salts, Porphyrins, Jacobsen-Katsuki oxidation, Salen, Peroxoacetic acid, P450 BM-3, Escherichia coli, lodosylbenzene, Oxometallacycle, DFT, Lewis acid mechanism, Metalladioxolane, Mimoun complex, Sheldon complex, Michaelis-Menten, Schiff bases. Redox mechanism. Oxygen-rebound mechanism, Spiro structure. 2008 Elsevier B.V. [Pg.4]

A10j Na Aqueous solution is a strong base. Incompatible with organic anhydrides, acrylates, alcohols, aldehydes, alkylene oxides, substituted allyls, cellulose nitrate, cresols, caprolactam solution, chlorocarbons, epichlorohydrin, ethylene dichloride, isocyanates, ketones, glycols, nitrates, phenols, vinyl acetate. Exothermic deconqjosition with maleic anhydride. May increase the explosive sensitivity of nitromethane. Attacks aluminum, copper, tin, and zinc. [Pg.45]