交联和变形对聚合物结晶和熔化的影响:分子动力学研究

IF 5.7 1区 化学 Q1 POLYMER SCIENCE
Macromolecules Pub Date : 2026-10-13 Epub Date: 2026-09-15 DOI:10.1021/acs.macromol.6c00181
Atmika Bhardwaj, Huzaifa Shabbir, Jens-Uwe Sommer, Marco Werner
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引用次数: 0

摘要

我们使用粗粒聚乙烯醇(CG-PVA)模型和分子动力学模拟研究了交联和纠缠聚合物在外部变形下的结晶。在单轴变形之后,系统以恒定速率冷却以形成半晶状态,随后以恒定速率加热以诱导熔化。对于未拉伸的体系,网状结对成核温度没有显著影响,但增加了非晶态部分,降低了熔融温度。单轴变形加速成核并显著提高结晶温度,交联越强的聚合物表现出更大的位移,这与取向顺序参数的增强有关。我们进一步比较了恒定应变和恒定应力条件下的冷却和加热循环。在恒定的应力下,结晶引起超出初始预拉伸的额外伸长,并导致加热时明显的机械滞后,这是可逆形状记忆材料的行为特征。
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 Crosslinking and Deformation on Polymer Crystallization and Melting: A Molecular Dynamics Study

Influence of Crosslinking and Deformation on Polymer Crystallization and Melting: A Molecular Dynamics Study

We investigate the crystallization of crosslinked and entangled polymers under external deformation using a coarse-grained poly(vinyl alcohol) (CG-PVA) model and molecular dynamics simulations. Following uniaxial deformation, the systems are cooled at a constant rate to form semicrystalline states and subsequently heated at a constant rate to induce melting. For unstretched systems, network junctions do not significantly affect the nucleation temperature but increase the amorphous fraction and reduce the melting temperature. Uniaxial deformation accelerates nucleation and markedly increases the crystallization temperature, with more strongly crosslinked polymers exhibiting larger shifts that correlate with an enhanced orientation order parameter. We further compare cooling and heating cycles under constant strain and constant stress conditions. Under constant stress, crystallization induces additional elongation beyond the initial pre-stretch and leads to pronounced mechanical hysteresis upon heating, a behavior characteristic of reversible shape-memory materials.

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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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