Bio-Inspired Hydrogen-Bond Cross-Link Strategy toward Strong and Tough Polymeric Materials

被引:144
作者
Song, Pingan [1 ,2 ]
Xu, Zhiguang [1 ]
Lu, Yuan [3 ]
Guo, Qipeng [1 ]
机构
[1] Deakin Univ, Inst Frontier Mat, Polymers Res Grp, Geelong, Vic 3220, Australia
[2] Zhejiang Agr & Forestry Univ, Coll Engn, Dept Mat, Hangzhou 311300, Zhejiang, Peoples R China
[3] Oak Ridge Natl Lab, Oak Ridge, TN 37830 USA
基金
美国国家科学基金会;
关键词
SPIDER SILK FIBRILS; MECHANICAL-PROPERTIES; STRENGTH; NANOCONFINEMENT; BEHAVIOR;
D O I
10.1021/acs.macromol.5b00673
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
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 (similar to 440 MPa), reduced modulus (similar to 22.5 GPa) in nanoindention tests, hardness (similar to 0.5 GPa), and great extensibility (similar to 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.
引用
收藏
页码:3957 / 3964
页数:8
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