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The polymerization of vinyl acetate in one-phase o/w microemulsions stabilized with Aerosol OT (AOT) is examined as a function of concentration and type of initiator (V-50 and KPS) and temperature. Conversions and reaction rates increase with increasing concentration of V-50 and temperature. Faster polymerization rates and higher conversions are achieved with KPS because of the different electrostatic interactions between the charged microemulsion droplets and the free radicals of KPS and V-50. Average molar masses and polydispersity indexes ( M̄ w / M̄ n ) are much smaller than those observed in emulsion polymerization using the same surfactant, even at high conversions. Analysis of the molar mass distribution indicates that chain-transfer reactions to monomer are the controlling chain-growth mechanism in the polymerization of vinyl acetate in AOT microemulsions at all conversions.
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Sosa et al. (2000) studied this question.
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