具有宏观层状双层结构的各向异性水凝胶的疲劳行为及膨胀效应

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Most Laboni Begum, Milena Lama, Wenqi Yang, Xiang Li, Md. Anamul Haque, Xueyu Li* and Jian Ping Gong*, 
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引用次数: 0

摘要

软质材料的长期使用需要对其在循环载荷条件下的疲劳机制和结构演变有深入的了解。在这项工作中,我们研究了一种各向异性水凝胶复合材料的疲劳抗力行为,该复合材料由嵌入弹性水凝胶基质中的周期性堆叠聚合双层组成。由于层状双分子层作为可逆牺牲键的有效能量耗散,水凝胶复合材料在单调载荷下表现出高韧性和自弹性。我们发现,在与单调加载试验相似的加载速率下,双层材料仅适度提高了疲劳阈值本身,但显著抑制了疲劳裂纹扩展速率。其中,每循环疲劳裂纹扩展长度仅为原始弹性水凝胶的万分之一。在完全膨胀的试样中,这种抗疲劳断裂能力的增强仅略有降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fatigue Behaviors of Anisotropic Hydrogels with a Macroscopic Lamellar Bilayer Structure and Swelling Effects

Fatigue Behaviors of Anisotropic Hydrogels with a Macroscopic Lamellar Bilayer Structure and Swelling Effects

The application of soft materials for long-term use requires a profound understanding of their fatigue mechanisms and structural evolution under cyclic loading conditions. In this work, we studied the fatigue resistance behaviors of an anisotropic hydrogel composite consisting of periodically stacked, polymerized bilayers embedded in an elastic hydrogel matrix. The hydrogel composite exhibits high toughness and self-resilience under monotonic loading due to efficient energy dissipation from the lamellar bilayers, which act as reversible sacrificial bonds. We found that at a loading rate similar to the monotonic loading test, bilayers only modestly enhance the fatigue threshold itself but significantly suppress the fatigue crack extension rate above the fatigue threshold. Specifically, the fatigue crack extension length per cycle is only 1/10,000 that of the pristine elastic hydrogel. This enhancement in fatigue fracture resistance is only modestly reduced in the fully swollen sample.

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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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