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Dielectric properties of polyarylate blends
Authors:T Nagasawa  Y Murata  K Tadano  R Kawai  K Ikehara  S Yano
Affiliation:(1) Unitika Ltd., Nihonbashi, Muromachi, Chuo-ku, Tokyo, 103-8321, Japan;(2) Osaka Prefectural College of Technology, Saiwai-cyo, Neyagawa, Osaka, 501-8572, Japan;(3) Gifu College of Medical Technology, Ichihiraga, Seki, Gifu, 501-3892, Japan;(4) Department of Chemistry, Faculty of Engineering, Gifu University, Yanagido, Gifu, 501-1193, Japan;(5) Department of Chemistry, Faculty of Engineering, Gifu University, Yanagido, Gifu, 501-1193, Japan
Abstract:Dielectric properties and molecular motion were studied by use ofdielectric spectroscopy and differential scanning calorimetry for twoblends, fully transesterificated polyarylate of bisphenol A withterephthalate/isophthalate (50/50) (PA)/polycarbonate of bisphenol A(PC) blends and PA/poly(ethylene terephthalate) (PET) blends. All thequenched PA/PC and PA/PET blends were amorphous and the glasstransition temperature (Tg) was varied with the blends ratioaccording to Gordon-Taylor equation. The PA/PET blends with more than60% of PET crystallized above the crystallization temperature. ThePA/PC and PA/PET blends showed two dielectric relaxations, agrabove Tg and gamma below Tg, which are related to a glasstransition and a local motion of short segment, respectively. Theagr relaxation moved to lower temperatures as PC or PET contentincreases, reflecting the lowering Tg faithfully. In the PA/PETblends, the static (epsiv0) and the limiting dielectricconstant (epsivinfin), and the increment (Deltaepsiv) for the agr relaxation decreases with increasingtemperature and the decrease falled on one curve, independent of theblend ratio. Any ferro- and piezoelectricity were not observed fortwo blends.
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