Non-conventional techniques for polymerization and depolymerization were investigated. The rates of polymerization were enhanced higher in ultrasonic, supercritical fluids and microwaves. However in these system under certain conditions, simultaneous degradation also occurred. Depolymerization was studied by various methods like thermal degradation in supercritical fluids and in presence of oxidizers, Lewis acid and other organic acids. Degradation by ultrasound and thermal degradation of polymer mixtures were also investigated. The scission of the polymer backbone is random for thermal degradation while the scission occurs at the midpoint for ultrasonic degradation. The degradation rates in all the investigated techniques were higher than the degradation rates observed for pyrolysis. Degradation was possible at low temperature (< 50°C) for oxidative and ultrasound degradation while the degradation rates were two orders of magnitude higher in supercritical conditions. The molecular weight distribution was obtained by GPC analysis and the continuous distribution models were used to obtain the rate coefficients. The activation energies were calculated from the temperature dependence of the rate coefficients.