Comparative investigation on radical polymerization of methyl and ethyl methacrylate under multi-site phase-transfer catalytic conditions

Methyl and ethyl methacrylate was polymerized in heterogeneous system with the help of newly synthesized multi-site phase-transfer catalyst and using water-soluble initiator at 60?±?1?°C under unstirred inert atmospheric condition. Polymer yield was increased with increasing molar concentrations of monomer, initiator, catalyst and temperature. Polymerization follows first-order kinetics with respect to monomer and half-order with respect to catalyst and initiator, respectively. PTC has myriads of applications in the synthesis of various organic and polymeric materials because of its fast reaction and high yield in short period of time. Without addition of PTC, polymerization did not occur; this indicates that catalyst plays the pivotal role on initiation of polymerization. It extracts the reactive radical anion from aqueous phase and transfers to the organic phase where acrylates were polymerized. Polymerization reactivity of methyl and ethyl methacrylate under PTC conditions was studied by various parameters. The activation energy (Ea) and other thermodynamic parameters were calculated. The Ea value supports the reactivity of acrylates. The results obtained from this investigation were used for inferring the radical mechanism of phase-transfer-catalyzed polymerization. The obtained polymers were analyzed by spectral and thermal analyses.