Highly stretchable, tough, and self-recoverable and self-healable dual physically crosslinked hydrogels with synergistic "soft and hard" networks

被引:12
|
作者
Li, Xuefeng [1 ,2 ]
Zhao, Youjiao [1 ]
Li, Dapeng [3 ]
Zhang, Gaowen [1 ]
Gao, Xiang [1 ]
Long, Shijun [2 ]
机构
[1] Hubei Univ Technol, Coll Mat & Chem Engn, Hubei Prov Key Lab Green Mat Light Ind, Wuhan 430068, Hubei, Peoples R China
[2] Hubei Univ Technol, Coll Mat & Chem Engn, Collaborat Innovat Ctr Green Light Weight Mat & P, Wuhan 430068, Hubei, Peoples R China
[3] Univ Massachusetts, Bioengn Dept, Coll Engn, N Dartmouth, MA 02747 USA
来源
POLYMER ENGINEERING AND SCIENCE | 2019年 / 59卷 / 01期
基金
中国国家自然科学基金;
关键词
FRACTURE; LINKING; GEL;
D O I
10.1002/pen.24880
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Strength, toughness and self-recoverability are among the most important properties of hydrogels for tissue-engineering applications. Yet, it remains a challenge to achieve these desired properties from the synthesis of a single-polymer hydrogel. Here, we report our one-pot, a monomer-polymerization approach to addressing the challenge by creating dual physically crosslinked hybrid networks, in particular, synergistic "soft and hard" polyacrylic acid-Fe3+ hydrogels (SHPAAc-Fe3+). Favorable mechanical properties achieved from such SHPAAc-Fe3+ hydrogels included high tensile strength (about 1.08 MPa), large elongation at break (about 38 times), excellent work of extension (about 19 MJ m(-3)), and full self-recoverability (100% recovery of initial properties within 15 min at 50 degrees C and within 60 min in ambient conditions, respectively). In addition, the hydrogels exhibited good self-healing capabilities at ambient conditions (about 40% tensile strength recovery without any external stimuli). This work demonstrates that dual physical crosslinking combining hydrophobic interaction and ionic association can be achieved in single-polymer hydrogels with significantly improved mechanical performance but without sacrificing favorable properties. POLYM. ENG. SCI., 59:145-154, 2019. (c) 2018 Society of Plastics Engineers
引用
收藏
页码:145 / 154
页数:10
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