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Glass transition phenomena in melt-processed polystyrene/polypropylene blends

机译:熔融加工的聚苯乙烯/聚丙烯共混物中的玻璃化现象

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摘要

Blends of an amorphous and a semi-crystalline polymer-polystyrene and polypropylene, respectively-were prepared by melt processing in an extruder at 220 degrees C. These polymers are known to be immiscible and the composite morphologies were characterized by electron microscopy and thermal analysis. Fine micron-scale morphologies, ranging from 0.5 to 20 microns were observed. Thermal analysis and dynamic mechanical analysis showed changes in both the polystyrene and polypropylene glass transition temperatures (T-g) over the composition range. The major effect was a sharp increase in polystyrene T-g with increasing polypropylene content in the blend. A T-g elevation of 5.5 degrees C was observed at 85% polypropylene. The polypropylene T-g also increases with increasing polypropylene content, starting at a depressed value in discrete polypropylene domain environments and approaching the bulk polypropylene value after the phase inversion is crossed. Qualitative structural models are proposed based on spatial and mechanical interactions between the components.
机译:通过在挤出机中于220摄氏度下进行熔融加工,分别制备了无定形和半结晶聚合物-聚苯乙烯和聚丙烯的共混物。已知这些聚合物是不溶混的,并且通过电子显微镜和热分析表征了复合物的形貌。观察到细微的微米级形态,范围从0.5到20微米。热分析和动态力学分析显示,在整个组成范围内,聚苯乙烯和聚丙烯玻璃化转变温度(T-g)均发生变化。主要影响是随着共混物中聚丙烯含量的增加,聚苯乙烯T-g急剧增加。在85%的聚丙烯上观察到5.5℃的T-g升高。聚丙烯的T-g也会随着聚丙烯含量的增加而增加,从离散的聚丙烯畴环境中的降低值开始,并在相转变结束后达到本体聚丙烯值。基于组件之间的空间和机械相互作用,提出了定性结构模型。

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