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Vinyl chloride, reaction

By contrast, addition polymers are those formed by the addition reaction of an unsaturated monomer, such as takes place in the polymerisation of vinyl chloride (Reaction 1.2). [Pg.5]

U.S. consumption pattern 1999, 3 619t U.S. producers, 3 610t vapor-phase nitration of, 17 257 vinyl chloride reactions with, 25 632 world production by country, 3 611-612t Benzene-based catalyst technology, 15 500 Benzene-based fixed-bed process technology, 15 505-506 Benzene chlorination process, of phenol manufacture, 18 751 m-Benzenedisulfonic acid, 3 602 p-Benzenedisulfonic acid, 3 602 Benzene feedstock, 23 329 Benzene hexachloride, 3 602 Benzene manufacture, toluene in, 25 180-181... [Pg.93]

Note A proprietary adaptation of this solvent to clean-up of vinyl chloride reaction vessels is available under trademark of M-Pyrol [GAF],... [Pg.842]

Af-vinyl carbazole, reaction type 212 vinyl chloride, reaction type 212 vinyl ester, reaction type 212 vinyl ether, reaction type 212 vinyl fluoride, reaction type 212 vinylidene, reaction type 212 chloride At-vinylpyrrolidone, reaction type 212 virus, tobacco necrosis, crystal structure 166... [Pg.874]

Polymerization conditions I mmole of initiator per mole of vinyl chloride reaction temperature as indicated polymerization by bulk technique under nitrogen of high purity. [Pg.375]

The choice of the proper peroxy initiator largely depends on its decomposition rate at the reaction temperature of the polymerization. BPO is the major initiator for bulk polymerization of polystyrene or acrylic ester polymers, where temperatures from 90°C to 220°C are encountered. Dilau-royl, dicaprylyl, diacecyl, and di- err-butyl peroxides are also used. In the case of suspension polymerization of styrene, where temperatures between 85°C and 120 C are applied, the initiators also range in activity from BPO to di-tm-butyl peroxide. In suspension polymerization of vinyl chloride (reaction temperatures of 45-60°C for the homopolymer), thermally very labile peroxides such as diisopropyl peroxydicarbonate and rm-butyl peroxy-pavilate are used. [Pg.42]


See other pages where Vinyl chloride, reaction is mentioned: [Pg.30]    [Pg.120]    [Pg.127]    [Pg.178]    [Pg.377]    [Pg.399]    [Pg.445]    [Pg.453]    [Pg.453]    [Pg.454]    [Pg.487]    [Pg.664]    [Pg.666]    [Pg.861]    [Pg.137]    [Pg.91]    [Pg.864]   
See also in sourсe #XX -- [ Pg.13 , Pg.155 ]




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