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表面活性剂在疏水界面吸附的表面增强拉曼光谱研究。

Surface-enhanced Raman spectroscopy studies of surfactant adsorption to a hydrophobic interface.

作者信息

Olson Lydia G, Harris Joel M

机构信息

Department of Chemistry, University of Utah, 315 South 1400 East, Salt Lake City, Utah 84112-0850, USA.

出版信息

Appl Spectrosc. 2008 Feb;62(2):149-56. doi: 10.1366/000370208783575492.

Abstract

Surface-enhanced Raman spectroscopy is used to investigate the kinetics of adsorption of the cationic surfactant cetylpyridinium chloride (CPC) to hydrophobic surfaces from water. A hydrophobic surface, with stable and reproducible SERS activity, is produced by binding gold colloids to an amine-terminated glass slide and then modifying this surface with octadecyltrimethoxysilane. In situ SERS-detected adsorption of CPC from aqueous solution is found to follow a Frumkin isotherm. Interactions between the charged head groups could be detected in frequency shifts in the symmetric ring breathing mode, consistent with an interfacial surfactant environment similar to a CPC micelle. Rates of surfactant adsorption were determined by time-resolved SERS measurements and were found to be much slower than the diffusion-controlled limit, indicating a significant kinetic barrier to adsorption. Desorption kinetics were heterogeneous, consistent with the spectroscopic results. Alkylsilane-modified gold colloids were shown to be useful substrates for investigating amphiphile adsorption from aqueous solutions to hydrophobic surfaces, where the adsorption kinetics could also be used to determine analyte concentrations in solution.

摘要

表面增强拉曼光谱用于研究阳离子表面活性剂十六烷基氯化吡啶(CPC)从水中吸附到疏水表面的动力学。通过将金胶体结合到胺基封端的载玻片上,然后用十八烷基三甲氧基硅烷修饰该表面,制备出具有稳定且可重复的表面增强拉曼散射(SERS)活性的疏水表面。原位SERS检测到的CPC从水溶液中的吸附遵循弗鲁姆金等温线。在对称环呼吸模式的频移中可以检测到带电头部基团之间的相互作用,这与类似于CPC胶束的界面表面活性剂环境一致。表面活性剂的吸附速率通过时间分辨SERS测量确定,发现其比扩散控制极限慢得多,表明存在显著的吸附动力学障碍。解吸动力学是不均匀的,这与光谱结果一致。烷基硅烷修饰的金胶体被证明是用于研究两亲物从水溶液吸附到疏水表面的有用底物,其中吸附动力学也可用于测定溶液中的分析物浓度。

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