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纳米孔中表面活性剂与疏水面的相互作用。

Interaction of surfactants with hydrophobic surfaces in nanopores.

机构信息

Department of Chemistry, The Nanoscience and Nanotechnology Institute, Center for Biocatalysis and Bioprocessing, University of Iowa, Iowa City, Iowa 52242, United States.

出版信息

Langmuir. 2010 Dec 21;26(24):19091-9. doi: 10.1021/la1031009. Epub 2010 Nov 2.

Abstract

Surfactant-induced wetting of hydrophobic nanopores is investigated. SDS micelles interact with the C18 layer on the nanopore walls with their hydrophobic tails, creating a charged wall lining with their head groups and inducing a breakthrough of the aqueous solution to wet the pores. The surface coverage of the surfactant molecules is evaluated electrophoretically. A surprising discovery is that pore wetting is achieved with 0.73 μmol/m(2) coverage of SDS surfactant, corresponding to only 18% of a monolayer on the walls of the nanopores. Clearly, the surfactant molecules cannot organize as a compact uninterrupted monolayer. Instead, formation of hemimicelles is thermodynamically favored. Modeling shows that, to be consistent with the experimental observations, the aggregation number of hemimicelles is lower than 25 and the size of hemimicelle is limited to a maximum radius of 11.7 Å. The hydrophobic tails of SDS thus penetrate into and intercalate with the C18 layer. The insight gained in the C18-surfactant interactions is essential in the surfactant-induced solubilization of hydrophobic nanoporous particles. The results have bearing on the understanding of the nature of hydrophobic interactions.

摘要

研究了表面活性剂诱导的疏水纳米孔润湿。SDS 胶束与纳米孔壁上的 C18 层通过其疏水尾部相互作用,形成带有头基的带电壁层,并诱导水溶液突破以润湿孔。通过电泳评估表面活性剂分子的表面覆盖率。一个令人惊讶的发现是,仅用 0.73 μmol/m(2)的 SDS 表面活性剂覆盖,就可以实现孔润湿,这仅相当于纳米孔壁上单分子层的 18%。显然,表面活性剂分子不能组织成紧密连续的单分子层。相反,形成部分胶束在热力学上是有利的。模拟表明,为了与实验观察结果一致,部分胶束的聚集数小于 25,并且部分胶束的尺寸限于 11.7 Å 的最大半径。因此,SDS 的疏水尾部会渗透到 C18 层中并嵌入其中。在 C18-表面活性剂相互作用方面获得的见解对于理解表面活性剂诱导的疏水性纳米颗粒的增溶作用至关重要。这些结果对于理解疏水性相互作用的性质具有重要意义。

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