材料科学
聚合物
乙二醇
韧性
制作
微尺度化学
甲基丙烯酸酯
复合材料
聚合
玻璃化转变
原位聚合
相(物质)
化学工程
医学
化学
替代医学
数学教育
数学
有机化学
病理
工程类
作者
Zhenwu Wang,Matthias Heck,Wenwu Yang,Manfred Wilhelm,Pavel A. Levkin
标识
DOI:10.1002/adfm.202300947
摘要
Abstract Polymer gels, consisting of cross‐linked polymer network systems swollen by a solvent, show great potential in biomedicine, flexible electronics, and artificial muscles, due to their tissue‐like mechanical properties. Due to the presence of a large amount of solvent, the improvement of the mechanical properties of the polymer gel is a challenge. Moreover, combining high toughness with useful properties, such as 3D printability or shape‐memory, in one polymer gel system is even more challenging. In this study, a simple and efficient method is developed for the fabrication of tough polymer gels by polymerizing 2‐hydroxyethyl methacrylate (HEMA) in a mixture of poly(ethylene glycol) (PEG) and poly(propylene glycol) (PPG). The polymerized elastic networkpresents distinct compatibility with PEG (compatible) and PPG (poorly compatible), resulting in in‐situ phase separation at the microscale. The resulting phase‐separated gel demonstrates high strength (8.0 MPa), favorable fracture strain (430%), and large toughness (17.0 MJ m −3 ). The separated hard phasewith a high glass transition temperature (75 °C) endows the whole soft polymer gel with the property of shape memory at room temperature. Finally, the fabrication of tunable tough PEGgels is combined with 3D printing as well as with shape memory properties, demonstrating the use of PEGgels for 4D printing.
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