材料科学
利乐
PEG比率
自愈水凝胶
极限抗拉强度
聚合
纳米复合材料
纳米技术
聚合物
化学工程
复合材料
高分子化学
化学
经济
药物化学
工程类
财务
作者
Lina Wang,Kun Lei,Zhao Li,Xinling Wang,Haijun Xiao,Zhen Zheng
标识
DOI:10.1002/mame.201800325
摘要
Abstract Further improving mechanical performances of the tetra‐PEG hydrogel and simultaneously endowing it with functionalities remains a challenge. Herein, rGO is introduced into the tetra‐PEG network to construct a tetra‐PEG/rGO nanocomposite (NC) hydrogel with improved mechanical performances and functionalities. The hydrogel is prepared by in situ simultaneous polymerization of clickable tetra‐PEG macromonomers (TAPEG and TPPEG) and reduction of GO in one pot. The amount of rGO introduced into the hydrogel network is determined and can be controlled through tuning the feed ratio of the GO to the macromonomers. The tetra‐PEG/rGO NC hydrogel displays drastically improved mechanical performances including tensile properties, compressive properties, and fatigue resistance compared to the pristine clickable tetra‐PEG hydrogel. SEM, FT‐IR, and loading–unloading experiments indicate that interactions between rGO sheets and tetra‐PEG segments contribute to the mechanical improvement. Furthermore, the tetra‐PEG/rGO NC hydrogel exhibits selective dye adsorption ability and near‐infrared light responsiveness. The tetra‐PEG/rGO NC hydrogel with excellent mechanical performances and functionalities is highly promising in many areas such as dye absorption, remote light‐controlled devices, and tissue engineering.
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