Silicone rubber composites filled with nano-silica are currently widely used as high voltage insulating materials in power transmission and substation systems. We present a systematic study on the dielectric and mechanical performance of silicone rubber filled with surface modified and unmodified fumed nano-silica. The results indicate that the different interfaces between the silicone rubber and the two types of nano-silica introduce changes in their dielectric response when electrically stressed by a sinusoidal excitation in the frequency range of 10−4–1 Hz. The responses of pure silicone rubber and the composite filled with modified silica can be characterized by a paralleled combination of Maxwell-Wagner-Sillars interface polarization and DC conduction. In contrast, the silicone rubber composite with the unmodified nano-silica exhibits a quasi-DC (Q-DC) transport process. The mechanical properties of the composites (represented by their stress-strain characteristics) reveal an improvement in the mechanical strength with increasing filler content. Moreover, the strain level of the composite with a modified filler is improved.

No abstract

No abstract

Capacitors and sensors based on polymer dielectric materials are key components in electrical systems and electronic devices. Considering the temperature rise during operation, an effective evaluation method for the thermal ageing of polymer matrix is urgently needed. P(VDF-HFP) film with a thickness of 20 μm is manufactured by solution casting and a thermal ageing experiment up to 1000 h is conducted. Dielectric responses of wide ranges of temperatures and frequencies are measured for samples with different ageing durations. The universal relaxation law and Dissado-Hill dielectric response model are applied to further investigate the results. The characteristics of individual processes are obtained, which demonstrate that the main chain relaxation following the Vogel−Fulcher −Tammann equation and side chain relaxation following the Arrhenius equation both remain unchanged after thermal ageing. However, the activation energies of those two processes change significantly during the process and show different variation trends. The activation energy of the side chain relaxation gets larger monotonically due to the influence of annealing and the breaking of crystalline region. As a result, a non-destructive evaluation method for the thermal ageing of P(VDF-HFP) is proposed accordingly.

No abstract