Line tension of alkane lenses on aqueous surfactant solutions at phase transitions of coexisting interfaces

被引:10
作者
Matsubara, Hiroki [1 ]
Ushijima, Baku [1 ]
Law, Bruce M. [2 ]
Takiue, Takanori [1 ]
Aratono, Makoto [1 ]
机构
[1] Kyushu Univ, Fac Sci, Dept Chem, Higashi Ku, Fukuoka 8128581, Japan
[2] Kansas State Univ, Dept Phys, Condensed Matter Lab, Manhattan, KS 66506 USA
关键词
Line tension; Surfactant; Alkane; Wetting transition; Surface phase transition; WETTING TRANSITION; WATER; FILMS; HEXADECANE; BEHAVIOR; 1ST-ORDER; DOMAINS; EQUILIBRIUM; MONOLAYERS; OIL;
D O I
10.1016/j.cis.2013.07.001
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
Alkane droplets on aqueous solutions of surfactants exhibit a first-order wetting transition as the concentration of surfactant is increased. The low-concentration or "partial wetting" state corresponds to an oil lens in equilibrium with a two-dimensional dilute gas of oil and surfactant molecules. The high-concentration or "pseudo-partial wetting" state consists of an oil lens in equilibrium with a mixed monolayer of surfactant and oil. Depending on the combination of surfactant and oil, these mixed monolayers undergo a thermal phase transition upon cooling, either to a frozen mixed monolayer or to an unusual bilayer structure in which the upper leaflet is a solid layer of pure alkane with hexagonal packing and upright chains while the lower leaflet remains a disordered liquid-like mixed monolayer. Additionally, certain long-chain alkanes exhibit a surface freezing transition at the air-oil interface where the top monolayer of oil freezes above its melting point. In this review, we summarize our previous studies and discuss how these wetting and surface freezing transitions influence the line tension of oil lenses from both an experimental and theoretical perspective. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:186 / 194
页数:9
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