首页> 外文期刊>Chemistry, an Asian journal >Bioinspired, Cysteamine-Catalyzed Co-Silicification of (1H, 1H, 2H, 2H- Perfluorooctyl)triethoxysilane and Tetraethyl Orthosilicate: Formation of Superhydrophobic Surfaces
【24h】

Bioinspired, Cysteamine-Catalyzed Co-Silicification of (1H, 1H, 2H, 2H- Perfluorooctyl)triethoxysilane and Tetraethyl Orthosilicate: Formation of Superhydrophobic Surfaces

机译:生物启发的半胱胺催化的(1H,1H,2H,2H-全氟辛基)三乙氧基硅烷和原硅酸四乙酯的共硅化:超疏水表面的形成

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Bioinspired silicification attracts a great deal of interest because of its physiologically relevant, mild conditions for hydrolysis and condensation of silica precursors, which makes the bioinspired approach superior to the conventional sol-gel process, particularly when dealing with biological entities. However, the morphological control of silica structures with incorporation of functional groups in the bioinspired silicilication has been unexplored. In this work, we co-silicificated (1H, 1H, 2H, 2H-perfluorooctyl)triethoxysilane and tetraethyl orthosilicate to investigate the morphological evolution of fluorinated silica structures in the cetyltrimethylammonium bromide-mediated, cysteamine-catalyzed silicification. The generated micrometer-long wormlike and spherical silica structures display superhydrophobicity after film formation. Interestingly, the measurement of dynamic water contact angles shows that the morphological difference leads to a different wetting state, either the self-cleaning or the pinning state of the superhydrophobic surface.
机译:由于生物启发的硅化作用具有生理相关性,温和的二氧化硅前体水解和缩合条件,因此引起了极大的兴趣,这使得生物启发的方法优于常规的溶胶-凝胶工艺,特别是在处理生物实体时。然而,尚未探索在生物启发的硅化中结合官能团的二氧化硅结构的形态控制。在这项工作中,我们共同硅化了(1H,1H,2H,2H-全氟辛基)三乙氧基硅烷和原硅酸四乙酯,以研究在十六烷基三甲基溴化铵介导的半胱胺催化的硅化反应中氟化二氧化硅结构的形态演变。成膜后,产生的微米级蠕虫状和球形二氧化硅结构显示出超疏水性。有趣的是,动态水接触角的测量表明,形态差异会导致不同的润湿状态,即超疏水表面的自清洁或钉扎状态。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号