How temperature-induced depolymerization and plasticization affect the process of structural relaxation

Abstract

The self-plasticization, i.e., the increase in the polymer segmental mobility by the inclusion of its own monomer, has a major impact on the structural, thermal, and mechanical properties of the polymer. Differential scanning calorimetry (DSC) was used to investigate the influence of thermally induced self-plasticization on the structural relaxation of polydioxanone (PDX). Depolymerization (based dominantly on the end-chain scission mechanism) was found to be controlled by the depolymerization temperature Td as well as the actual number of re-melting cycles (while keeping the time spent at Td constant). PDX samples with the glass transition temperature (Tg) ranging from −52 (highly plasticized) to −13 °C (virgin) were prepared. The DSC data were described in terms of the Tool-Narayanaswamy model; a consistent structural relaxation behavior associating the degree of plasticization with Tg was identified. The activation energy first decreased with plasticization from 430 kJ mol−1 to 210 kJ mol−1 in the Tg range of −40 to −13C, which is consistent with the plasticization-caused spacing-apart of the polymer chains resulting in larger free volume and increased freedom for the relaxation movements. For the highly plasticized PDX samples, the activation energy increased from 210 kJ mol−1 to 310 kJ mol−1, which appears to be associated with the possible segregation of the portion of the plasticizer into a discrete phase. The width of the relaxation times distribution increased with plasticization as a consequence of the plasticizer loosening the polymeric chains and enabling a wider variety of the segmental movement. The plasticization also leads to a higher dependence of the segmental relaxation movements on their current physico-chemical and steric surrounding.