Large strain hysteresis and mullins effect of tough double-network hydrogels

被引:677
作者
Webber, Rebecca E.
Creton, Costantino [1 ]
Brown, Hugh R.
Gong, Jian Ping
机构
[1] ESPCI, UPMC, CNRS, UMR 7615,Lab Physicochim Polymeres & Milieux Disp, F-75005 Paris, France
[2] Univ Wollongong, Fac Engn, Wollongong, NSW 2522, Australia
[3] Hokkaido Univ, Dept Biol Sci, Lab Soft & Wet Matter, Sapporo, Hokkaido 060, Japan
关键词
D O I
10.1021/ma062924y
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理]; 080501 [材料物理与化学]; 081704 [应用化学];
摘要
Systematic loading and unloading experiments, in uniaxial tension and uniaxial compression, have been performed on a double-network hydrogel exhibiting a very high toughness. We observed a significant hysteresis during the first loading cycle that increased strongly with the applied maximum deformation. A large hysteresis was not observed during a second loading cycle, implying that the initial hysteresis can be attributed to the fracture of covalent bonds in the primary network. We report this type of dissipative mechanism for polymer gels for the first time. Assuming that the entire energy dissipated during the hysteresis cycle can be attributed to the fracture of network strands by a Lake-Thomas mechanism, our results suggest that the fracture and unloading of only 1% of the bonds within the network leads to a decrease of up to 80% of the number of strands. These results also demonstrate the very large degree of heterogeneity within the hydrogel network. If such a dissipative mechanism is active at the crack tip, it will most likely greatly increase the energy necessary to propagate a macroscopic crack, elucidating the origin of the toughness in these interesting materials.
引用
收藏
页码:2919 / 2927
页数:9
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