Copolymers, unsaturation Styrene-divinyl benzene

McKillop [117] found that the application of pyrolysis-gas chromatography to the determination of unsaturation in vulcanisation had serious disadvantages. Vinyl groups in styrene-divinyl benzene copolymer have been determined by pyrolysis-mass spectrometry. 

Styrene-1,3-butadiene copolymers with higher styrene contents (50-70%) are used in latex paints. Styrene and 1,3-butadiene terpolymerized with small amounts of an unsaturated carboxylic acid are used to produce latexes that can be crosslinked through the carboxyl groups. These carboxylated SBR products are used as backing material for carpets. Styrene copolymerized with divinyl benzene yields crosslinked products, which find use in size-exclusion chromatography and as ion-exchange resins (Sec. 9-6). 

Polystyrene is imusual among commodity polymers in that we can prepare it in a variety of forms by a diversity of polymerization methods in several types of reaction vessel. Polystyrene may be atactic, isotactic, or syndiotactic. Polymerization methods include free radical, cationic, anionic, and coordination catalysis. Manufacturing processes include bulk, solution, suspension, and emulsion polymerization. We manufacture random copolymers by copolymerizing styrene directly vith comonomers containing vinyl groups. In addition, we can polymerize styrene in the presence of polymer chains containing unsaturation in order to create block copolymers. Crosslinked varieties of polystyrene can be produced by copolymerizing styrene vith difunctional monomers, such as divinyl benzene. 

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