材料科学
自愈水凝胶
相容性(地球化学)
复合材料
韧性
模数
极限抗拉强度
聚合物
弹性模量
纤维素
断裂韧性
限制
杨氏模量
动态力学分析
聚合物网络
蠕动
细菌纤维素
拉伸试验
作者
Shuxing Yin,Guojun Che,Cheng Qian,Can Zhou,Shengwen Kong,Chuangqi Zhao,Lu Jiang
摘要
ABSTRACT The double‐network strategy is a classic approach for preparing the hydrogels with high mechanical performance. However, the poor modulus compatibility between the rigid and soft polymers causes rigid network stress concentration and irreversible fracture, thus ultimately limiting hydrogels applicability. Here, we propose a strategy to fabricate strong and tough double‐network hydrogel by regulating modulus compatibility and reinforcing interfacial interactions between poly(vinyl alcohol) and cellulose nanofibers. The introduction of tannic acid not only enables decrease of modulus of CNF rigid network within the double‐network hydrogel, but also reinforces the noncovalent interactions between the double networks, leading to the improvement of mechanical properties. The resulted hydrogel exhibits an extremely high tensile strength of 39.7 ± 1.7 MPa and an outstanding toughness of 155.2 ± 2.5 MJ m −3 . Furthermore, the double‐network hydrogel has excellent fracture energy, fatigue resistance and biocompatibility. This work provides a practical avenue to design strong and tough hydrogels that can be exploited for biomedical application.
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