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Deformation-Induced Crystallization Behavior of Isotactic Polypropylene Sheets Containing a β-Nucleating Agent under Solid-State Stretching

机译:固态拉伸下含β-成核剂的全同立构聚丙烯片材的变形诱导结晶行为

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摘要

The deformation-induced crystallization of an isotactic polypropylene (iPP) sheet containing a β-nucleating agent was evaluated. The phase transformation of the β-modifications was investigated and the crystal morphology was observed at room temperature after stretching at different temperatures. The results showed that the crystallinity increased after solid-state stretching. When the stretching temperature was below the initial crystallization temperature, stretching deformation promoted the orientation of amorphous molecular chains. When the deformation temperature exceeded the crystallization temperature, part of the β-modifications underwent a phase transformation process and was stretched into a shish-kebab structure. However, once the stretching temperature was close to the melting point, the β-modifications melted and recrystallized, and the shish-kebab structure underwent stress relaxation due to poor thermal stability, transforming into α-modifications. It was revealed that the crystal phase transformation mechanism of the β-modifications was based on the orientation of the molecular chains between the adjacent lamellae. In addition, the shish-kebab cylindrite structure played an important role in modifying the tensile and impact properties of the iPP sheet. The tensile and impact strengths increased by as much as 34% and 126%, respectively.
机译:评价了含有β成核剂的全同立构聚丙烯(iPP)片的变形诱导结晶。研究了β-修饰物的相变,并在不同温度下拉伸后在室温下观察到晶体形态。结果表明,固态拉伸后结晶度增加。当拉伸温度低于初始结晶温度时,拉伸变形促进了无定形分子链的取向。当变形温度超过结晶温度时,部分β-变体经历了相变过程并且被拉伸成烤肉串结构。然而,一旦拉伸温度接近熔点,则β-变体熔化并重结晶,并且由于热稳定性差,烤肉串结构经历应力松弛,转变为α-变体。揭示了β-修饰的晶体相变机理是基于相邻薄片之间的分子链的取向。此外,烤肉串的圆柱形结构在改变iPP片材的拉伸和冲击性能方面起着重要作用。拉伸强度和冲击强度分别增加了34%和126%。

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