配位牺牲键强度对聚酯增韧性能的影响

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Jie Chen, Sheng Wang, Jie Huan, Zhikai Li, Xiaoming Yang, Xiaohong Li* and Yingfeng Tu*, 
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引用次数: 0

摘要

通过悬挂的特吡啶(TPY)配体与过渡金属离子配位形成超分子交联点作为牺牲键(SB),从物理交联的半结晶聚酯中构建了双交联体系。通过使用不同的离子(Fe2+、Co2+、Ni2+、Cu2+ 和 Zn2+),研究了配位相互作用强度对增韧效果的影响。结果表明,配位键越强,杨氏模量越大,但强度和韧性则不然,在达到最佳 SB 强度的最大值后,强度和韧性先增大后减小。这是由于在不同的应变下,超分子交联点和物理交联点的性能表现不同。我们的研究结果表明,SB 强度并不是越高越好,这对设计高强度和高韧性材料很有帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of Coordination Sacrificial Bond Strength on Toughening Properties of Polyesters

Effect of Coordination Sacrificial Bond Strength on Toughening Properties of Polyesters

Effect of Coordination Sacrificial Bond Strength on Toughening Properties of Polyesters

By the coordination of dangling terpyridine (TPY) ligands with transition metal ions to form supramolecular cross-linking points as sacrificial bonds (SBs), a double-cross-linked system is constructed from the physically cross-linked semicrystalline polyesters. The mechanical properties are greatly enhanced, and the effect of coordination interaction strength on the toughening effect has been investigated by using different ions (Fe2+, Co2+, Ni2+, Cu2+, and Zn2+). It shows that stronger coordination bonds provide a larger Young’s modulus, but not for strength and toughness, which increase first and then decrease after achieving a maximum value at an optimal SB strength. This is due to the properties estimated at different strains, where the supramolecular and physically cross-linking points behave differently. Our results demonstrate that SB strength is not the higher, the better, which should be useful for the design of strong and tough 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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