Primary piezoelectric relaxation in copolymers of β-hydroxybutyrate and β-hydroxyvalerate

Y. Ando, M. Minato, K. Nishida, E. Fukada
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引用次数: 0

Abstract

Oriented films of a copolymer of 75 mol% ß-hydroxybutyrate and 25 mol% ß-hydroxyvalerate produced from microorganism showed intrinsic shear piezoelectricity. Complex piezoelectric constant e=e'-ie", elastic constant c= c'+ ic" and dielectric constant ε= ε' — iε" were dynamically determined at 0.8–100 Hz and at −40 −40°C. Relaxational behaviors of these quantities were observed around glass transition temperature. Assuming time-temperature equivalence, master curves for these three constants were well composed. The temperature variation of shift factor fitted well to WLF equation. The theory of spherical dispersion model, in which piezoelectric crystalline are dispersed in relaxing amorphous medium, was satisfactorily applied for the piezoelectric relaxation.
β-羟基丁酸酯和β-羟基戊酸酯共聚物的初级压电弛豫
由微生物制备的75 mol% ß-羟丁酸酯和25 mol% ß-羟戊酸酯共聚物定向膜表现出固有的剪切压电性。复合压电常数e=e′-ie”,弹性常数c= c′+ ic”和介电常数ε= ε′- iε”在0.8 ~ 100 Hz和- 40 ~ 40℃下动态测定。在玻璃化转变温度附近观察了这些量的弛豫行为。假设时间-温度等效,这三个常数的主曲线组成良好。位移因子的温度变化符合WLF方程。压电晶体分散在松弛的非晶介质中的球形色散模型理论在压电弛豫研究中得到了满意的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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