Kinetics of the Thermal and Thermo-Oxidative Degradation of Polystyrene, Polyethylene and Poly(propylene)

TLDR

The study interprets the obtained dependencies in terms of degradation mechanisms. Thermal degradations of PS, PE, and PP were studied in nitrogen and air using thermogravimetry and differential scanning calorimetry, and a model‑free isoconversional method was applied to calculate activation energies as a function of degradation extent. Under nitrogen, PS, PE, and PP degrade via random scission with activation energies of ~200, 240, and 250 kJ mol⁻¹ respectively, while initial stages show lower energies (~150 kJ mol⁻¹) indicating initiation at weak links; in air, thermoxidative degradation proceeds through peroxide decomposition with activation energies of 125, 80, and 90 kJ mol⁻¹ for PS, PE, and PP.

Abstract

The thermal degradations of polystyrene (PS), polyethylene (PE), and poly(propylene) (PP) have been studied in both inert nitrogen and air atmospheres by using thermogravimetry and differential scanning calorimetry. The model-free isoconversional method has been employed to calculate activation energies as a function of the extent of degradation. The obtained dependencies are interpreted in terms of degradation mechanisms. Under nitrogen, the thermal degradation of polymers follows a random scission pathway that has an activation energy ≈200 kJ·mol–1 for PS and 240 and 250 kJ·mol–1 for PE and PP, respectively. Lower values (≈150 kJ·mol–1) are observed for the initial stages of the thermal degradation of PE and PS; this suggests that degradation is initiated at weak links. In air, the thermoxidative degradation occurs via a pathway that involves decomposition of polymer peroxide and exhibits an activation energy of 125 kJ·mol–1 for PS and 80 and 90 kJ·mol–1, for PE and PP respectively.