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

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Jianlan Ye*, Minghao Liu, Jing Hu and Jay Oswald*, 
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Abstract

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.

Abstract Image

拓扑段长度对半晶聚乙烯力学性能的影响:偏置控制蒙特卡罗方法
我们将偏置机制集成到混合蒙特卡罗方法中,使生成具有可控拓扑段长度的半晶系统成为可能。对生成的体系的分析揭示了桥梁长度和形成的桥梁数量之间的熵驱动关系。我们发现桥梁显著增强了场后硬化,并且桥梁诱导硬化可分为四个阶段:松弛、激活、接合和软化。结果表明:桥梁长度决定了接合应变,从而决定了桥致硬化的发生;推导了基于桥梁初始构型和体系尺寸的啮合应变预测方程。软化阶段发生在晶体茎另一侧共价连接的尾部和环被深深拉入晶体片层,削弱桥的锚定。此外,具有较长环的系统形成更多的桥接缠结,这就像长桥一样,在变形的后期阶段加强了硬化效果。
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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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