Cruz Barrios Eliandreina, Annunziata Onofrio
Department of Chemistry and Biochemistry, Texas Christian University, 2950 W. Bowie St., Sid Richardson Bldg. #438, Fort Worth, Texas 76129, United States.
Langmuir. 2021 Mar 2;37(8):2855-2862. doi: 10.1021/acs.langmuir.1c00176. Epub 2021 Feb 17.
Micellization is a phenomenon of central importance in surfactant solutions. Here, we demonstrate that the diffusion-based spreading of the free boundary between a micellar aqueous solution and pure water yields a one-dimensional spatial profile of surfactant concentration that can be used to identify the critical micelle concentration, here denoted as *. This can be achieved because dilution of micelles into water leads to their dissociation at a well-defined position along the concentration profile and an abrupt increase in the diffusion coefficient. Rayleigh interferometry was successfully employed to determine * values for three well-known surfactants in water at 25 °C: Triton X-100 (TX-100), sodium dodecyl sulfate (SDS), and poly(oxyethylene)(4)Lauryl Ether (Brij-30). The dependence of * on salt concentration was also characterized for TX-100 in the presence of NaSO, NaCl, and NaSCN. Accurate values of * can be directly identified by visual inspection of the corresponding concentration-gradient profiles. To apply the method of least squares to experimental concentration profiles, a mathematical expression was derived from Fick's law and the pseudophase separation model of micellization with the inclusion of appropriate modifications. While Rayleigh interferometry was employed in our experiments, this approach can be extended to any experimental technique that yields one-dimensional profiles of surfactant concentration. Moreover, diffusion-driven surfactant disaggregation is precise, noninvasive, requires single-sample preparation, and applies to both nonionic and ionic surfactants. Thus, this work provides the foundation of diffusion-driven dilution methods, thereby representing a valuable addition to existing techniques for the determination of *.
胶束化是表面活性剂溶液中至关重要的一种现象。在此,我们证明胶束水溶液与纯水之间基于扩散的自由边界扩展会产生表面活性剂浓度的一维空间分布,该分布可用于确定临界胶束浓度,在此记为*。之所以能够实现这一点,是因为胶束在水中稀释会导致它们在沿浓度分布的明确位置解离,并且扩散系数会突然增加。成功地使用瑞利干涉测量法来测定25℃时水中三种知名表面活性剂的值:聚乙二醇辛基苯基醚(TX - 100)、十二烷基硫酸钠(SDS)和聚氧乙烯(4)月桂醚(Brij - 30)。还研究了在硫酸钠、氯化钠和硫氰化钠存在下TX - 100的对盐浓度的依赖性。通过目视检查相应的浓度梯度分布可以直接确定的准确值。为了将最小二乘法应用于实验浓度分布,从菲克定律和胶束化的假相分离模型出发,并进行适当修改,推导得到了一个数学表达式。虽然我们的实验中使用了瑞利干涉测量法,但这种方法可以扩展到任何能产生表面活性剂浓度一维分布的实验技术。此外,扩散驱动的表面活性剂解聚精确、非侵入性,只需单一样品制备,并且适用于非离子和离子表面活性剂。因此,这项工作为扩散驱动的稀释方法奠定了基础,从而为现有的测定技术增添了有价值的内容。