The effect of alkane tail length of CiE8 surfactants on transport to the silicone oil-water interface

被引:28
作者
Alvarez, Nicolas J. [1 ]
Lee, Wingki [1 ]
Walker, Lynn M. [1 ]
Anna, Shelley L. [1 ,2 ]
机构
[1] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Mech Engn, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
Dynamic surface tension; Oil-water interfaces; Nonionic surfactants; Adsorption; Transport; Timescales; ADSORPTION-KINETICS; NONIONIC SURFACTANTS; AIR; DIFFUSION; TENSION; EQUATION; STATE; MECHANISMS; DESORPTION; EXCHANGE;
D O I
10.1016/j.jcis.2010.11.077
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Detailed surfactant transport studies have typically been restricted to the air-water interface. This is mainly due to the lack of experimental devices and techniques available to study liquid-liquid interfaces. As a result, there is a lack of relevant data and understanding of surfactant behavior in microfluidic studies and emulsion applications. Using a novel shape fitting algorithm for a pendant drop capable of handling fluids of similar densities, i.e. low Bond numbers, we measure the dynamic surface tension as a function of bulk surfactant concentration at the silicone oil-water interface for a homologous series of CiE8 nonionic surfactants. We show that the isotherms governing equilibrium at the oil-water and air-water interfaces are very different. Using a scaling analysis comparing two governing mass transport timescales, we demonstrate that there exists a transition from diffusion-limited to kinetic-limited dynamics at the silicone oil-water interface. Adsorption rate constants are determined from a one parameter nonlinear fit to dynamic surface tension data. These results demonstrate that the dynamics of interfacial transport are highly dependent on the immiscible fluids that form the interface. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:231 / 236
页数:6
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