Abstract

Thermally stimulated depolarization current (TSDC) measurement was used to investigate the liquid–liquid transition process of atactic polystyrene (aPS). There are four distinct peaks (α, ρ 1, LL and ρ 2) showed in TSDC spectrum in the range of 300–480 K. Compared with the result of differential scanning calorimetry for aPS, the TSDC spectrum showed that the peak LL located at 422 K could be attributed to the movement of entire chain related to liquid–liquid transition. The isolated peak LL was separated from TSDC spectrum of aPS by curve fitting procedure of the kinetics equation. The distribution of relaxation time of liquid–liquid transition was obtained in terms of the principle of Debye relaxation process. Based on analysis of calculated results, it was confirmed that the relaxation time during the liquid–liquid transition of aPS changed gradually from following Vogel–Fulcher equation to Arrhenius rule with increasing temperature.

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