Adsorption kinetics of surfactant mixtures from micellar solutions as studied by maximum bubble pressure technique

被引:41
作者
Frese, C
Ruppert, S
Sugár, M
Schmidt-Lewerkühne, H
Wittern, KP
Fainerman, VB
Eggers, R
Miller, R
机构
[1] Beiersdorf AG, D-20245 Hamburg, Germany
[2] Donetsk Med Univ, Med Physicochem Ctr, UA-83003 Donetsk, Ukraine
[3] Tech Univ Hamburg, D-21073 Hamburg, Germany
[4] Max Planck Inst Colloids & Interfaces, D-14424 Golm, Germany
关键词
surfactant adsorption; anionic cationic mixtures; micellar solutions; dynamic surface tensions; bubble pressure tensiometry;
D O I
10.1016/S0021-9797(03)00614-3
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
The adsorption kinetics of micellar solutions of anionic/cationic SDS/DATB mixtures with mixing ratios of 10/1 and 10/2, respectively, are studied experimentally by means of the maximum bubble pressure method. For long adsorption times the adsorption of the highly surface-active anionic/cationic complex leads to a decrease of dynamic surface tension in comparison to the single SDS system. However, the situation is the reverse for short adsorption times where the dynamic surface tension is increased by addition of the cationic surfactant, although the overall concentration is increased. This unexpected behavior is explained by partial solubilization of free SDS molecules into micelles formed by SDS/DTAB complexes. With increasing overall concentration, when eventually the CMC of SDS is reached, the anionic/cationic complex itself is solubilized by SDS micelles. Finally, no complex micelles, which for their part can solubilize an excess of SDS molecules, are present. Hence, the dynamic properties of the solution are no longer influenced by the depletion of SDS molecules and the mixture tends to behave like a pure SDS solution. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:475 / 482
页数:8
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