Molecular weight distributions in radiation‐induced polymerization. V. A simultaneous kinetic and molecular weight distribution analysis of the liquid‐state polymerization of styrene

Abstract

AbstractThe γ‐ray initiated polymerization of styrene in the liquid state was investigated over the temperature range 0 to −29°C at constant dose rate. The kinetics and molecular weight distributions were studied for samples prepared by standard techniques and samples subjected to exhaustive drying to remove residual water. In the former case, the rates of reaction were comparable to those for purely free radical polymerization, however, the resulting molecular weight distributions were distinctly bimodal, indicating an additional contribution from the cationic mechanism. On the other hand, the rates of polymerization for rigorously dried samples were 2 to 3 orders of magnitude greater than accepted free‐radical values, and the molecular weight distributions were unimodal in nature. The experimental results were compared with theoretical kinetic data and molecular weight distribution data generated from a kinetic scheme taking into consideration polymerization via free‐radical, cationic, and radical‐cationic species, resulting in the evaluation of a number of quantities of interest. Substitution of determined values for the rate constants and G values results in good agreement between theoretically generated and experimentally determined kinetic data and molecular weight distribution data over the range of experimental conditions studied.