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通过动态力学测量和介电谱研究聚偏氟乙烯的弛豫动力学。

Relaxation dynamics of poly(vinylidene fluoride) studied by dynamical mechanical measurements and dielectric spectroscopy.

作者信息

Sencadas V, Lanceros-Méndez S, Sabater i Serra R, Andrio Balado A, Gómez Ribelles J L

机构信息

Centro de Física/Departamento de Física, Universidade do Minho, Campus de Gualtar, 4710-058 Braga, Portugal.

出版信息

Eur Phys J E Soft Matter. 2012 May;35(5):41. doi: 10.1140/epje/i2012-12041-x. Epub 2012 May 30.

Abstract

The aim of this study is to analyze the mobility of polymer chains in semicrystalline poly(vinylidene fluoride) (PVDF). PVDF crystallizes from the melt in the α crystalline phase. The transformation from the α phase to the electroactive β phase can be induced by stretching at temperatures in the range between 80 and 140 °C. The spherulitic structure of the crystalline phase is deformed during stretching to form fibrils oriented in the direction of the strain. The amorphous phase confined among the crystalline lamellae is distorted as well and some degree of orientation of the polymer chains is expected. Dynamic-mechanical and dielectric spectroscopy measurements were performed in PVDF films stretched to strain ratios up to 5 at temperatures between 80 and 140 °C. Dynamic-mechanical measurements were conducted between -60 °C and melting and in this temperature range the relaxation spectra show the main relaxation of the amorphous phase (called β-relaxation) and at higher temperatures a relaxation related to crystallites motions (α (c)-relaxation). Although the mean relaxation times of the β-relaxation are nearly equal in PVDF before and after crystal phase transformation, a significant change of shape of the relaxation spectrum proves the effect of chain distortion due to crystal reorganization. In stretched PVDF the elastic modulus of the polymer in the direction of deformation is significantly higher than in the transversal one, as expected by chain and crystals fibril orientation. The recovery of the deformation when the sample is heated is related with the appearance of the α (c)-relaxation. Dielectric spectroscopy spectrum shows the main relaxation of the amorphous phase and a secondary process (γ-relaxation) at lower temperatures. Stretching produces significant changes in the relaxation processes, mainly in the strength and shape of the main relaxation β. The Havriliak-Negami function has been applied to analyze the dielectric response.

摘要

本研究的目的是分析半结晶聚偏二氟乙烯(PVDF)中聚合物链的流动性。PVDF从熔体中结晶形成α晶相。在80至140°C的温度范围内拉伸可诱导α相向电活性β相的转变。结晶相的球晶结构在拉伸过程中变形,形成沿应变方向取向的原纤维。限制在结晶薄片之间的非晶相也会发生扭曲,预计聚合物链会有一定程度的取向。在80至140°C的温度下,对拉伸至应变比高达5的PVDF薄膜进行了动态力学和介电谱测量。动态力学测量在-60°C至熔点之间进行,在此温度范围内,弛豫谱显示了非晶相的主要弛豫(称为β弛豫),在较高温度下,有一个与微晶运动相关的弛豫(α(c)弛豫)。尽管在晶相转变前后,PVDF中β弛豫的平均弛豫时间几乎相等,但弛豫谱形状的显著变化证明了晶体重组导致的链扭曲效应。在拉伸的PVDF中,聚合物在变形方向上的弹性模量明显高于横向弹性模量,这与链和晶体原纤维的取向预期一致。样品加热时变形的恢复与α(c)弛豫的出现有关。介电谱显示了非晶相的主要弛豫和较低温度下存在的二级过程(γ弛豫)。拉伸会使弛豫过程产生显著变化,主要是主弛豫β的强度和形状。已应用Havriliak-Negami函数来分析介电响应。

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