A Self-Healing Cellulose Nanocrystal-Poly(ethylene glycol) Nanocomposite Hydrogel via Diels-Alder Click Reaction

被引:208
|
作者
Shao, Changyou [1 ]
Wang, Meng [1 ]
Chang, Huanliang [1 ]
Xu, Feng [1 ]
Yang, Jun [1 ]
机构
[1] Beijing Forestry Univ, Beijing Key Lab Lignocellulos Chem, 35 Tsinghua East Rd, Beijing 100083, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Self-healing hydrogels; Cellulose nanocrystals (CNCs); Diels-Alder (DA) reaction; CROSS-LINKING; STEP-POLYMERS; CHEMISTRY; NANOCRYSTALS; BONDS; POLYMERIZATION; MONOMERS; DYNAMICS; MOIETIES; CHITOSAN;
D O I
10.1021/acssuschemeng.7b01060
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-healing hydrogels are particularly desirable for increased safety and functional lifetimes because of stress-induced deformation and propagation of cracks. In this paper, we report a tough, highly resilient, fast self-recoverable, and self-healing nanocomposite hydrogel, which builds an interpenetrated network encapsulating rod-like cellulose nanocrystals (CNCs) by flexible polymer chains of poly(ethylene glycol) (PEG). A thermally reversible covalent Diels-Alder click reaction between furyl-modified CNCs and maleimide-end-functionalized PEG was confirmed by Fourier transform infrared spectroscopy. Uniaxial tensile tests and unconfined compression tests displayed outstanding mechanical properties of the hydrogels with a high fracture elongation up to 690% and a fracture strength up to 0.3 MPa at a strain of 90%. Cyclic loading unloading tests showed excellent self-recovery and antifatigue properties of the nanocomposite hydrogels. The self-healing capability of nanocomposite hydrogels assessed by tension tests was found to be as high as 78%. The self-healing CNC-PEG nanocomposite hydrogels would shed insight into designing reusable and renewable polymeric hydrogels.
引用
收藏
页码:6167 / 6174
页数:8
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