Dual-faced borax mediated synthesis of self-healable hydrogels merging dynamic covalent bonding and micellization

被引:9
作者
Li, Xiaohui [1 ,2 ]
Mutlu, Hatice [2 ]
Fengler, Christian [1 ]
Wilhelm, Manfred [1 ]
Theato, Patrick [1 ,2 ]
机构
[1] Karlsruhe Inst Technol KIT, Inst Chem Technol & Polymer Chem ITCP, Engesserstr 18, D-76131 Karlsruhe, Germany
[2] Karlsruhe Inst Technol KIT, Inst Biol Interfaces 3 IBG 3, Soft Matter Synth Lab, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
关键词
ACID-BASED HYDROGELS; THIOL-ENE CLICK; TOUGH; MICELLES; DELIVERY;
D O I
10.1039/d0py01354d
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Intrinsic self-healing hydrogels with excellent mechanical properties are still difficult to achieve. Here, we presented a facile method to integrate dynamic boronate ester bonds and Pluronic F127 (PF127) micelle cross-links into one hydrogel system via a borax catalyzed thiol-ene click reaction and borax-diol chemistry. The hydrogel was capable of elongating up to 340% and self-healing approximately 90% of its initial stress within 24 h. Moreover, the hydrogel could endure a compressive strain of 80% without fracture, and exhibited excellent shape recovery and fatigue resistance ability as determined by the cyclic compressive loading-unloading test at 60% strain, providing a new facile route to design multifunctional hydrogels with spontaneous self-healing ability, good stretchability and excellent compressive properties.
引用
收藏
页码:361 / 369
页数:10
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