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Synthesis of graft polymers from an ozonised ethylene‐vinyl acetate copolymer, 2. Determination of the efficiency and of the decomposition rate of macroinitiators
Author(s) -
Fargère Thierry,
Abdennadher Mohamed,
Delmas Michel,
Boutevin Bernard
Publication year - 1994
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.1994.021950518
Subject(s) - polymer chemistry , copolymer , polymerization , styrene , vinyl acetate , radical polymerization , polymer , chemistry , chain transfer , polystyrene , thermal decomposition , ethylene , monomer , radical , materials science , organic chemistry , catalysis
Abstract Polymers can be treated with an ozone/oxygen mixture to create peroxide and hydroperoxide groups on the polymer chain. These heat‐sensitive functional groups can serve to initiate radical polymerization of vinyl monomers to form graft copolymers. The efficiency and the decomposition rate constant of an ozonized ethylene‐vinyl acetate copolymer (EVA) are determined using the polymerization rate of styrene. The thermal polymerization of styrene is studied in the presence of non‐ozonized EVA. The thermal polymerization has no effect on the polymerization of styrene at the beginning of the reaction. Transfer reactions between the growing polystyrene radical and the EVA chain are negligible. The activation energy of the decomposition rate of ozonized EVA is calculated and reaches 46 kJ/mol. The entropy variation of the decomposition reaction is also calculated. The result obtained shows an important decrease (−45 cal · mol −1 · K −1 ) of the entropy which is opposite to the common behaviour (−6 to +13 cal · mol −1 · K −1 ) expected. The efficiency observed for the ozonized polymers is low and reaches only 20% at 100°C, this can be explained by the lack of mobility of the created radicals.