首页> 外文会议>Electroactive polymer actuators and devices (EAPAD) 2016 >Temperature Dependent Impedance Spectroscopy and Thermally Stimulated Depolarization Current (TSDC) Analysis of Disperse Red 1-co-Poly(methyl methacrylate) Copolymers
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Temperature Dependent Impedance Spectroscopy and Thermally Stimulated Depolarization Current (TSDC) Analysis of Disperse Red 1-co-Poly(methyl methacrylate) Copolymers

机译:分散红1-共聚(甲基丙烯酸甲酯)共聚物的温度依赖性阻抗谱和热激发去极化电流(TSDC)分析

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摘要

The dielectric relaxation processes of polymethyl methacrylates that have been functionalized with Disperse Red 1 (DR1) in the side chain (DR1-co-MMA) were studied with temperature dependent impedance spectroscopy and thermally stimulated depolarization current (TSDC) techniques. Copolymers with dipole contents which varied between 10 mol% and 70 mol% were prepared. All samples showed dipole relaxations above the structural-glass transition temperature (T_g). The β-relaxation of the methyl methacrylate (MMA) repeating unit was most visible in DRl(10%)-co-MMA and rapidly vanishes with higher dipole contents. DSC data reveal an increase of the T_g by 20 ℃ to 125℃ with the inclusion of the dipole into the polymethyl methacrylate (PMMA) as side chain. The impedance data of samples with several DR1 concentrations, taken at several temperatures above T_g , have been fitted with the Havriliak-Negami (HN) function. In all cases, the fits reveal a dielectric response that corresponds to power-law dipolar relaxations. TSDC measurements show that the copolymer can be poled, and that the induced polarization can be frozen by lowering the temperature well below the glass transition. Relaxation strengths Ae estimated by integrating the depolarization current are similar to those obtained from the impedance data, confirming the efficient freezing of the dipoles in the structural-glass state.
机译:使用依赖于温度的阻抗谱和热激发去极化电流(TSDC)技术研究了已在侧链上用分散红1(DR1)功能化的聚甲基丙烯酸甲酯的介电弛豫过程。制备偶极子含量在10mol%至70mol%之间变化的共聚物。所有样品均显示出高于结构玻璃化转变温度(T_g)的偶极弛豫。甲基丙烯酸甲酯(MMA)重复单元的β松弛在DR1(10%)-co-MMA中最明显,并且偶极含量较高时迅速消失。 DSC数据显示,随着偶极子作为侧链进入聚甲基丙烯酸甲酯(PMMA)中,T_g从20℃升高到125℃。在高于T_g的多个温度下采集的具有几种DR1浓度的样品的阻抗数据已与Havriliak-Negami(HN)函数拟合。在所有情况下,拟合都显示出与幂律偶极弛豫相对应的介电响应。 TSDC测量表明,该共聚物可以极化,并且可以通过将温度降低到远低于玻璃化转变温度而冻结诱导的极化。通过积分去极化电流估算出的弛豫强度Ae与从阻抗数据获得的弛豫强度Ae相似,证实了偶极子在结构玻璃状态下的有效冻结。

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  • 来源
  • 会议地点 Las Vegas NV(US)
  • 作者单位

    Swiss Federal Laboratories for Materials Science and Technology Empa, Laboratory for Functional Polymers, UEberlandstr. 129, CH-8600, Duebendorf, Switzerland,Ecole Polytechnique Federate de Lausanne (EPFL), Institut des materiaux, Station 12, CH 1015, Lausanne, Switzerland;

    Swiss Federal Laboratories for Materials Science and Technology Empa, Laboratory for Reliability, Science and Technology, UEberlandstr. 129, CH-8600, Duebendorf, Switzerland,Swiss Federal Institute of Technology (ETH), CH-8093 Zuerich, Switzerland;

    Swiss Federal Laboratories for Materials Science and Technology Empa, Laboratory for Functional Polymers, UEberlandstr. 129, CH-8600, Duebendorf, Switzerland,Ecole Polytechnique Federate de Lausanne (EPFL), Institut des materiaux, Station 12, CH 1015, Lausanne, Switzerland;

    Swiss Federal Laboratories for Materials Science and Technology Empa, Laboratory for Functional Polymers, UEberlandstr. 129, CH-8600, Duebendorf, Switzerland;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Disperse Red 1; TSDC; impedance spectroscopy; PMMA; dielectric relaxation; poling;

    机译:分散红1; TSDC;阻抗谱; PMMA;介电弛豫极化;

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