Adsorption kinetics of ionic surfactants with detailed account for the electrostatic interactions .1. No added electrolyte

被引:33
|
作者
Vlahovska, PM
Danov, KD
Mehreteab, A
Broze, G
机构
[1] UNIV SOFIA,FAC CHEM,LAB THERMODYNAM & PHYSICOCHEM HYDRODYNAM,BU-1126 SOFIA,BULGARIA
[2] COLGATE PALMOLIVE TECHNOL CTR,PISCATAWAY,NJ 08854
[3] COLGATE PALMOL R&D INC,B-4041 MILMORT,BELGIUM
关键词
ionic surfactants; adsorption kinetics; dynamic surface tension;
D O I
10.1006/jcis.1997.4919
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 problem of diffusion-controlled adsorption from a nonmicellar solution of an ionic surfactant in the absence of added electrolyte is solved analytically for the case of small deviations from equilibrium. For that purpose the electro-diffusion equations of the transport of surfactant ions and counterions are combined with the Poisson-Boltzmann equation for the electrical held, The resulting set of equations is linearized and Laplace transform is applied. Analytical expression for the Laplace image of the adsorption is obtained in terms of elementary functions. Simple formulae for the short-time and long-time asymptotics of adsorption and surface tension relaxation are derived. To illustrate the effect of the electrostatic Interactions we calculated the theoretical dependence of the characteristic relaxation time on the bulk surfactant concentration and surface potential for aqueous surfactant solutions in contact with various non-aqueous phases (air, heptane, decane, petroleum ether) and two surfactants: SDS and DTAB. The general trend is that the electrostatic effects decelerate the process of adsorption, as it could be expected. The derived exact analytical expressions quantifying these effects can be directly applied for the interpretation of experimental data for the kinetics of ionic surfactant adsorption. The reliability of our approach is verified through a comparison with other available theories. (C) 1997 Academic Press.
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页码:194 / 206
页数:13
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