Unusual wetting dynamics of aqueous surfactant solutions on polymer surfaces

被引:86
作者
Dutschk, V
Sabbatovskiy, KG
Stolz, M
Grundke, K
Rudoy, VM
机构
[1] Inst Polymer Res eV, D-01069 Dresden, Germany
[2] Russian Acad Sci, Inst Phys Chem, Moscow 119991, Russia
[3] Sasol Germany GmbH, D-45764 Marl, Germany
关键词
wetting kinetics; aqueous surfactant solutions; polymer surfaces;
D O I
10.1016/S0021-9797(03)00723-9
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
Static and dynamic contact angles of aqueous solutions of three surfactants-anionic sodium dodecyl sulfate (SDS), cationic dodecyltrimethylammonium bromide (DTAB), and nonionic pentaethylene glycol monododecyl ether (C12E5)-were measured in the pre- and micellar concentration ranges on polymer surfaces of different surface free energy. The influence of the degree of substrate hydrophobicity, concentration of the solution, and ionic/nonionic character of surfactant on the drop spreading was investigated. Evaporation losses due to relatively low humidity during measurements were taken into account as well. It was shown that, in contrast to the highly hydrophobic surfaces, contact angles for ionic surfactant solutions on the moderately hydrophobic surfaces strongly depend on time. As far as the nonionic surfactant is considered, it spreads well over all the hydrophobic polymer surfaces used. Moreover, the results obtained indicate that spreading (if it occurs) in the long-time regime is controlled not only by the diffusive transport of surfactant to the expanding liquid-vapor interface. Obviously, another process involving adsorption at the expanding solid-liquid interface (near the three-phase contact line), which goes more slowly than diffusion, has to be active. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:456 / 462
页数:7
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