Changyou ShaoMeng WangHuanliang ChangFeng XuJun Yang
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.
Changyou Shao (4090093)Meng Wang (124646)Huanliang Chang (4090096)Feng Xu (89016)Jun Yang (2084)
KennethChristopher Koehler (1995016)Kristi S. Anseth (151212)Christopher N. Bowman (1265787)
Kenneth Christopher KoehlerKristi S. AnsethChristopher N. Bowman
Xinxin LiuKexin YangMinmin ChangXiaohui WangJunli Ren
Kai HouYan LiYao LiuRuihui ZhangBenjamin S. HsiaoMeifang Zhu