自愈水凝胶
材料科学
聚乙烯
环氧乙烷
自组装
氧化物
自愈
化学工程
高分子化学
乙烯
纳米技术
复合材料
聚合物
共聚物
化学
有机化学
冶金
替代医学
医学
工程类
催化作用
病理
作者
Erwan Nicol,Taco Nicolaï,Jingwen Zhao,Tetsuharu Narita
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2018-05-24
卷期号:7 (6): 683-687
被引量:13
标识
DOI:10.1021/acsmacrolett.8b00317
摘要
Homogeneous hydrogels were formed by self-assembly of triblock copolymers via association of small hydrophobic end blocks into micelles bridged by large poly(ethylene oxide) central blocks. A fraction of the end blocks were photo-cross-linkable and could be rapidly cross-linked covalently by in situ UV irradiation. In this manner networks were formed with well-defined chain lengths between homogeneously distributed hybrid micelles that contained both permanent and dynamically cross-linked end blocks. Linear rheology showed a single relaxation mode before in situ irradiation intermediate between those of the individual networks. The presence of transient cross-links decreased the percolation threshold of the network rendered permanent by irradiation and caused a strong increase of the elastic modulus at lower polymer concentrations. Large amplitude oscillation and tensile tests showed significant increase of the fracture strain caused by the dynamic cross-links.
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