首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >GLASS TRANSITION BEHAVIOUR OF POLY(ETHER ETHER KETONE) POLY(ETHER IMIDE) BLENDS
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GLASS TRANSITION BEHAVIOUR OF POLY(ETHER ETHER KETONE) POLY(ETHER IMIDE) BLENDS

机译:聚(醚酮)聚(醚酰亚胺)共混物的玻璃化转变行为

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摘要

Differential scanning calorimetry (d.s.c.), dynamic mechanical thermal analysis (d.m.t.a.) and dielectric relaxation spectroscopy (DRS) have been used to study the a-relaxation in amorphous blends of poly(ether ether ketone) (PEEK) and poly(ether imide) (PEI). The composition dependence of the d.s.c. T-g is well described by the Couchman and Gordon-Taylor equations while the isothermal dielectric loss curves can be fitted by the empirical Havriliak-Negami (HN) function. The HN parameters can be represented in the form of cooperativity plots which show that they do not follow a weighted average with changing composition. The time scale for dipolar relaxation in the blends is dominated by PEI, which relaxes at a relatively slower rate compared with PEEK, while the composition dependence of the apparent activation energy shows a negative deviation from additive behaviour. It is likely that these observations are related to the interactions between the blend components which result in changes in the local molecular environment on blending. [References: 27]
机译:差示扫描量热法(dsc),动态机械热分析(dmta)和介电弛豫谱(DRS)已用于研究聚醚醚酮(PEEK)和聚醚酰亚胺无定形共混物中的a-松弛( PEI)。 d.s.c.的成分依赖性T-g由Couchman和Gordon-Taylor方程很好地描述,而等温介电损耗曲线可以由经验Havriliak-Negami(HN)函数拟合。 HN参数可以以协作图的形式表示,该图显示它们在组成变化时不遵循加权平均值。共混物中偶极弛豫的时间尺度主要由PEI决定,与PEEK相比,PEI的弛豫速度相对较慢,而表观活化能的成分依赖性显示其与添加剂行为的负偏差。这些观察结果可能与共混物组分之间的相互作用有关,这会导致共混时局部分子环境的变化。 [参考:27]

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