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Creep-resistant behavior of beta-polypropylene with different crystalline morphologies

机译:β-聚丙烯的抗蠕变行为,具有不同的结晶形态

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摘要

β-Phase isotactic polypropylene (β-iPP) specimens with different contents of β-phase nucleating agent were employed to investigate the deformation-induced microstructure evolution during creep behavior. Morphological investigations by SEM showed that the crystalline morphologies of β-iPP were controlled by the content of the β-phase nucleating agent, namely, well-developed β-spherulites induced by low content of β-phase nucleating agent, bundle-like morphology with imperfect spherulites induced by medium content of β-phase nucleating agent and needle-like morphology induced by high content of β-phase nucleating agent. It was interesting to observe that all samples with different contents of β-phase nucleating agent showed a similar β/α transformation process. However, well-developed β-spherulites, which have integrated crystalline structure, showed poor creep resistance compared with the crystalline morphology nucleated by higher contents of β-phase nucleating agent. For bundle-like morphology, the crystalline phase was imperfect and obtained larger long spacing, resulting in better creep resistance. With respect to needle-like morphology, the crystalline phase was disordered and displayed largest long spacing, resulting in best creep resistance. The results of this work revealed that the creep resistance would be different with different crystalline morphologies. On the other hand, this work provided the evolution of microstructure during deformation to further explain the molecular mechanism of fatigue failure for creep.
机译:采用β相单位聚丙烯(β-IPP)具有不同β相成核剂的样品,用于研究蠕变行为期间的变形诱导的微观结构演化。通过SEM的形态学研究表明,β-IPP的结晶形态由β相成核剂的含量控制,即通过低含量的β相成核剂诱导的β-球晶型良好的β-球晶,与之束状形态通过高含量的β相成核剂诱导的β相成核剂的中含量和针状形态诱导的不完美的球晶。观察到具有β相成核剂的不同含量的所有样品显示出类似的β/α转化过程。然而,具有集成晶体结构的培养β-球晶,与通过β相成核剂的含量含量含量的晶体形态相比,较差的蠕变性。对于类似束形态的形态,结晶相是不完美的,得到较大的长距离,导致抗蠕变性更好。关于针状形态,结晶相是无序的并且显示最大的长距间距,导致最佳的抗蠕变性。这项工作的结果表明,蠕变抗性与不同的结晶形态不同。另一方面,这项工作提供了变形过程中微观结构的演变,以进一步解释蠕变疲劳失效的分子机制。

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