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首页> 外文期刊>Journal of Applied Polymer Science >Tailoring the Viscoelasticity of Epoxy Thermosets
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Tailoring the Viscoelasticity of Epoxy Thermosets

机译:量身定制环氧热固性树脂的粘弹性

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摘要

This research work is aimed to understand the effect of epoxy resin chemistry on the viscoelasticity of the cured epoxy thermosets. In this article, two model systems are selected based on epoxy-amine reactants. In the model Systems I, the functionality of the epoxy is varied. In model System II, the pendant (side) chain length in the amine is varied. It is found that by varying the initial properties (e.g., functionality, pendant chain length, mixing ratio (r), aromaticity, etc.) the network properties (crosslink density and flexibility) of the cured (or hardened) epoxy changed. The changes (or shift) in the viscoelastic properties (or viscoelasticity) of the cured epoxy is mainly due the changes in the network properties. Further, to study the time and temperature effects the viscoelastic master curves for the two model systems are generated using Time-Temperature-Superposition (TTS) principle. The shift in the viscoelastic master curves is modeled with a simple Kohlrausch-Williams-Watts (KWW) fit function.
机译:这项研究工作旨在了解环氧树脂化学对固化的环氧树脂热固性树脂粘弹性的影响。在本文中,基于环氧胺反应物选择了两种模型系统。在系统I模型中,环氧树脂的功能是可变的。在系统II型中,胺中侧链(侧链)的长度是变化的。发现通过改变初始性质(例如,官能度,侧链长度,混合比(r),芳香性等),固化(或硬化)的环氧树脂的网络性质(交联密度和挠性)改变。固化环氧树脂的粘弹性(或粘弹性)的变化(或变化)主要是由于网络性质的变化。此外,为了研究时间和温度影响,两个模型系统的粘弹性主曲线是使用时间-温度-叠加(TTS)原理生成的。粘弹性主曲线的移动是通过简单的Kohlrausch-Williams-Watts(KWW)拟合函数建模的。

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