聚对苯对苯二甲酰胺(PPTA)中位错扩展和应力传递的研究

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Ran Chen, Chuanfu Luo* and Xiaoniu Yang*, 
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引用次数: 0

摘要

位错在决定材料的变形中起着至关重要的作用,但在聚合物中仍然很少被探索。采用全原子分子动力学模拟,直接分析了聚对苯二甲酸乙二胺(PPTA)在外力作用下的准一维位错的独特结构,这与金属中的准一维位错有很大的不同。位错在聚合物纤维中的传播发生在两个不同的阶段:缓慢的内部传播和随后在链端快速扩展。所有结果表明,聚合物纤维的最终强度是由位错而不是化学键断裂决定的。应力传递和位错传播之间的关系表明,位错是由局部运动过程引起的,需要一个特定的应力水平来克服与位错相关的能量势垒。聚合物中位错的独特性质超越了特定的材料类别,提供了普遍适用的见解,如聚对苯对苯二甲酸乙二胺(PPTA),聚乙烯(PE)和聚酰胺(PA6)所证实的那样。我们的研究结果提供了对聚合物中位错动力学的深入理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Propagation of Dislocations and Stress Transmission in Poly(p-phenylene terephthalamide) (PPTA)

Propagation of Dislocations and Stress Transmission in Poly(p-phenylene terephthalamide) (PPTA)

Dislocations play a crucial role in determining the deformation of materials yet are still rarely explored in polymers. Employing all-atom molecular dynamics simulations, we directly analyzed the unique structure of quasi-1D dislocations in poly(p-phenylene terephthalamide) (PPTA) induced by an external force, which is drastically different from those in metals. The propagation of dislocations in polymer fibers occurs in two distinct stages: the slow internal propagation and the subsequent rapid extension at chain ends. All results reveal that the ultimate strength of polymer fibers is determined by dislocations rather than breaking chemical bonds. The relationship between stress transmission and dislocation propagation reveals that dislocations are caused by localized motion processes, necessitating a specific stress level to overcome the energy barrier associated with dislocations. The unique nature of dislocations in polymers transcends specific material categories, offering universally applicable insights, as verified by poly(p-phenylene terephthalamide) (PPTA), polyethylene (PE), and polyamide (PA6). Our results provide an in-depth understanding of the dislocation kinetics in polymers.

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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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