韧性
材料科学
聚合物
复合材料
氢键
交叉连接
极限抗拉强度
粘结强度
模数
可扩展性
纳米复合材料
分子
胶粘剂
有机化学
化学
计算机科学
图层(电子)
操作系统
作者
Pingan Song,Zhiguang Xu,Yuan Lü,Qipeng Guo
出处
期刊:Macromolecules
[American Chemical Society]
日期:2015-06-03
卷期号:48 (12): 3957-3964
被引量:161
标识
DOI:10.1021/acs.macromol.5b00673
摘要
It remains a huge challenge to create advanced polymeric materials combining high strength, great toughness, and biodegradability so far. Despite enhanced strength and stiffness, biomimetic materials and polymer nanocomposites suffer notably reduced extensibility and toughness when compared to polymer bulk. Silk displays superior strength and toughness via hydrogen bonds (H-bonds) assembly, while cuticles of mussels gain high hardness and toughness via metal complexation cross-linking. Here, we propose a H-bonds cross-linking strategy that can simultaneously strikingly enhance strength, modulus, toughness, and hardness relative to polymer bulk. The H-bond cross-linked poly(vinyl alcohol) exhibits high yield strength (∼140 MPa), reduced modulus (∼22.5 GPa) in nanoindention tests, hardness (∼0.5 GPa), and great extensibility (∼40%). More importantly, there exist semiquantitive linear relationships between the number of effective H-bond and macroscale properties. This work suggests a promising methodology of designing advanced materials with exceptional mechanical by adding low amounts (≤1.0 wt %) of small molecules multiamines serving as H-bond cross-linkers.
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