Thermal stabilization activities of metal oxide γ-Irradiated Styrene–Isoprene–Styrene nanocomposites

Abstract

This study provides insights into the stabilization effects of certain oxides (CeO2, Cr2O3, Cd2O3, In2O3, MnO2, MgO, Nd2O3, and Pr2O3) in styrene–isoprene–styrene triblock copolymers with respect to neat materials. This study was performed via chemiluminescence (CL), which allowed for the determination of the main parameters characterizing the interphase coexistence: the oxidation induction times, oxidation rates, and onset oxidation temperatures. The improvement in the thermal performances of the pristine and γ-ray-processed samples at a moderate dose was highlighted differently due to the electronic interactions on the particle surface. While the non-isothermal CL measurements pointed to a weaker evolution of oxidation in the studied composites at a higher temperature range over 160 ◦C, the isothermal CL determinations revealed a delayed start of oxidation, slower oxidation rates, and greater activation energies in the nanocomposite aging patterns. The different individual behaviors of the investigated formulations were ascribed to the dissimilar electronic interactions between the particles and the surrounding matrix, where the oxidation initiators were formed by the molecular fragmentation of the polymer macromolecules. The kinetic features illustrate the influence of the peculiarities due to the electronic interactions. The higher resistance shown by the irradiated samples compared with the non-processed compositions demonstrates the stabilization efficiency of the fillers studied.