Journal
EUROPEAN POLYMER JOURNAL
Volume 48, Issue 4, Pages 830-840Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.eurpolymj.2012.02.001
Keywords
Dielectric relaxation; Dielectric breakdown; Fluorinated polycarbonate; Ab initio SCF; High pressure; Low temperature
Categories
Funding
- US Office of Naval Research
- Department of Defense-Army Research Office [DAAD19-01-1-0482]
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The relative permittivity, loss and dielectric strength have been measured for a polycarbonate-based material, tetraaryl bisphenol A polycarbonate, that has been fluorine substituted (DiF p-TABPA-PC). The new material has a glass transition temperature, T-g = 489 K, that is higher than that for either conventional bisphenol A polycarbonate (BPA-PC) for which T-g = 421 K or for a copolymer of tetraaryl bisphenol A (TABPA) and bisphenol A (BPA) (TABPA-BPA-PC) for which T-g = 464 K. In addition, the dielectric strength of DiF p-TABPA-PC is almost identical to that for purified BPA-PC and slightly larger than the value for TABPA-BPA-PC. The relative permittivity and loss measurements were carried out from 10 to 10(5) Hz over a wide temperature range and at pressures up to 0.25 GPa. Variable temperature results for the alpha relaxation and both temperature and pressure results for the gamma relaxation regions are reported. The alpha relaxation exhibits standard behavior. The gamma relaxation exhibits unusual characteristics such as a strong increase in peak height as temperature increases and a strong decrease in peak height with increasing pressure. The data for the gamma relaxation have been analyzed using several formulations. Expressions for the peak height and peak position based on a two state (inequivalent well) model and the resulting parameters are discussed in terms of the insight they provide into the molecular mechanisms responsible for the sub-T-g relaxation. Ab initio SCF results for a related model compound are presented. Finally, the real part of the relative permittivity for the new polymer is about 10% higher than for BPA-PC. (C) 2012 Elsevier Ltd. All rights reserved.
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