Radiation crosslinking and scission of poly(vinyl methyl ether) in aqueous solution

Abstract

For a wide range of poly(vinyl methyl ether) (PMVE) concentrations (1–16 g dm −3), in anoxic conditions, polymer-derived radicals recombine in two major pathways: (i) crosslinking and (ii) disproportionation. Both these processes proceed inter- and intramolecularly. The radiation-chemical yields and kinetics of crosslinking have been studied by pulse radiolysis with light scattering intensity detection (LSI). In the absence of oxygen, G-values of intermolecular crosslinking were determined on the basis of LSI changes versus applied dose and compared with the results obtained previously for γ-irradiated samples. It has been found that the first half-life time of intermolecular crosslinking decreases with increasing dose per pulse. Addition of small amounts of macroradical scavenger (cysteamine hydrochloride) decreases, drastically, the increase of LSI signal. On increasing the PVME concentration, intermolecular crosslinking becomes more efficient. In the presence of oxygen, for diluted PVME solution (0.1 g dm −3), decrease of LSI signal consisting of the kinetic of a first-order reaction was observed. The rate constant of LSI decrease was found to be 1.1×10 3 s −1 and it was attributed to the main-chain scission.