IF 5.1 1区 化学 Q1 POLYMER SCIENCE
Jianlan Ye, Minghao Liu, Jing Hu, Jay Oswald
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引用次数: 0

摘要

我们在混合蒙特卡洛方法中加入了偏置机制,从而生成了拓扑段长度可控的半晶体系统。对生成系统的分析表明,桥段长度与形成的桥段数量之间存在熵驱动关系。我们发现,桥接可显著增强屈服后硬化,桥接引起的硬化可分为四个阶段:松弛、活化、啮合和软化。结果表明,桥的长度决定了啮合应变,从而决定了桥诱导硬化的开始时间;根据桥的初始配置和系统尺寸推导出了预测啮合应变的方程。软化阶段的发生是由于结晶茎另一侧共价连接的尾部和环部被深深拉入结晶薄片,从而削弱了桥的锚定。此外,具有较长环路的体系会形成更多的桥接缠结,就像长桥一样,在变形的后期阶段会加强硬化效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Influence of Topological Segment Length on the Mechanical Properties of Semicrystalline Polyethylene: A Bias-Controlled Monte Carlo Approach

Influence of Topological Segment Length on the Mechanical Properties of Semicrystalline Polyethylene: A Bias-Controlled Monte Carlo Approach
We integrate a biasing mechanism into the hybrid Monte Carlo method that enables the generation of semicrystalline systems with controllable topological segment length. Analysis of the generated systems revealed an entropy-driven relationship between the bridge length and the number of bridges formed. We find that bridges significantly enhance postyield hardening, and the bridge-induced hardening can be divided into four stages: relaxed, activation, engaged, and softening. The results show that lengths of bridges govern the engagement strain and thereby the onset of bridge-induced hardening; an equation is derived to predict the engagement strain based on bridges’ initial configurations and the system sizes. The softening phase occurs as the covalently connected tails and loops on the other side of the crystalline stems are pulled deeply into the crystalline lamellae, weakening the anchors of bridges. Additionally, systems with longer loops form more bridging entanglements, which, like long bridges, strengthen the hardening effect during the later stages of deformation.
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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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