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Predicting the visco-elastic properties of polystyrene/SIS composite blends using simple analytical micromechanics models

机译:使用简单的分析微观力学模型预测聚苯乙烯/ sIs复合材料混合物的粘弹性

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摘要

This paper is concerned with the prediction of the viscoelastic properties of rubber filled polymer blends. The question asked was as follows. Can the temperature dependent viscoelastic properties of phase separated polymer blends be adequately predicted using only a rational two phase micromechanics based analytical model with no empirical fitting parameters? In particular using only a knowledge of the individual bulk phase properties and the blend microstructure, but without any further detailed polymer physics knowledge such as the presence of an interphase region or any additional nanoscale structures within the separated rubber phase with the properties different from those of the two bulk phases? Blends of a polystyrene matrix and phase separated rubber inclusions (a polystyrene-polyisoprene-polystyrene triblock polymer (SIS)) were manufactured in a range of blend fractions (up to 20 vol % of the triblock co-polymer). Experimental measurements, for the storage modulus G′ and the loss tangent tanδ, of both the individual phases and the blends, were made using dynamic mechanical tests over a range of temperatures from −50 to +70 °C. Numerical predictions, of the same parameters, were first obtained using the generalised self-consistent Christensen and Lo model which uses a simple representative volume element (RVE) of an isolated sphere of the minority rubber component in a surrounding sheath of polystyrene matrix embedded in a homogeneous effective medium. The agreement between the Christensen and Lo model and the experimental measurements, for G′ and tanδ, was found to be excellent for rubber contents up to 10%. For a 20% rubber content, an improved prediction was obtained by altering the RVE to include the observed effect of having a polystyrene central core in a number of the dispersed rubber zones at this rubber fraction, using the Herve and Zaoui generalization of the Christensen and Lo model. Although conjoined (and therefore non-spherical) zones became more prevalent at the highest rubber content, use of the Tandon and Weng model showed that this shape anisotropy would not be expected to affect the viscoelastic properties.
机译:本文涉及橡胶填充聚合物共混物粘弹性的预测。提出的问题如下。是否可以仅使用基于理性的两相微力学的,没有经验拟合参数的分析模型来充分预测相分离的聚合物共混物的温度依赖性粘弹特性?特别是仅使用单个本体相特性和共混物微观结构的知识,而没有任何其他更详细的聚合物物理知识,例如分离的橡胶相中存在相间区域或任何其他纳米级结构,而这些性质与两个批量阶段?聚苯乙烯基质和相分离的橡胶夹杂物(聚苯乙烯-聚异戊二烯-聚苯乙烯三嵌段聚合物(SIS))的共混物以一定范围的共混物比例(最高为三嵌段共聚物的20体积%)制造。使用动态力学测试在-50至+70°C的温度范围内对各个相和共混物的储能模量G'和损耗正切tanδ进行了实验测量。首先使用广义的自洽Christensen和Lo模型获得相同参数的数值预测,该模型使用嵌入在管道中的聚苯乙烯基体周围护套中少数橡胶组分的隔离球的简单代表性体积元素(RVE)。均质有效介质。对于G'和tanδ,发现Christensen和Lo模型与实验测量值之间的一致性对于橡胶含量高达10%而言是极好的。对于20%的橡胶含量,使用Christensen的Herve和Zaoui归纳法,通过改变RVE来获得改进的预测,方法是将RVE更改为包括在该橡胶级分的多个分散橡胶区域中具有聚苯乙烯中心核的观察到的效果。罗模型。尽管在最高橡胶含量下,连带(因此非球形)区域变得更加普遍,但使用Tandon和Weng模型显示,这种形状各向异性将不会影响粘弹性。

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