Relaxation processes determining the electret stability of high-impact polystyrene/titanium-dioxide composite films

Abstract

The influence of relaxation processes on the thermal electret stability of high-impact polystyrene (HIPS) free-standing films filled with titanium dioxide (TiO2) of the rutile modification are investigated by means of a combination of dielectric methods (dielectric relaxation spectroscopy (DRS), thermally stimulated depolarization current (TSDC) and thermally stimulated surface-potential decay (TSSPD)), supplemented by differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA). Films with 2, 4, 6 and 8 vol.% TiO2 are compared to each other and to non-filled samples. Filling HIPS with up to 8 vol.% of TiO2 enhances the elastic modulus below the glass transition and increases the thermal electret stability above the glass transition without significantly increasing the DC conductivity. The improvement of the electret stability is caused by the build-up of an interface polarization which decays only gradually if the glass transition is exceeded. Two kinds of Arrhenius processes are considered in order to explain the decay of the composite-polymer electrets: (1) charge release from chemical traps located at the phenyl rings of the polymer chain with an activation energy of Ea = 1.1 eV after passing the glass transition at about 100 °C and (2) charge release from traps formed by the TiO2 particles with Ea = 2.4 eV at temperatures above 130 °C. Finally, the activation energies are discussed with respect to their significance.