Adsorption at the liquid/liquid interface in mixed systems with hydrophobic extractants and modifiers 2. Dynamic interfacial tension at the hydrocarbon/water interface in binary mixed systems

被引:15
|
作者
Staszak, K [1 ]
Prochaska, K [1 ]
机构
[1] Poznan Univ Technol, Inst Chem Technol & Engn, PL-60965 Poznan, Poland
关键词
liquid/liquid interface; dynamic interfacial tension; solvent extraction; hydrophobic metal ion extractants; mixed adsorbed monolayer; diffusion coefficient;
D O I
10.1016/j.jcis.2005.07.038
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 dynamic interfacial tension for binary mixtures of hydrophobic metal ion extractants and a modifier were measured by using the drop volume technique. Four types of equimolar mixtures were considered: two chelating extractants: 2-hydroxy-5-nonylacetophenone oxime (HNAF) and beta-diketone (1-phenyldecan- 1,3-dion), two solvating extractants: trioctylphosphine oxide (TOPO) and tributyl phosphate (TBP), chelating and solvating extractants TOPO and beta-diketone, and the chelating extractant HNAF and the modifier (decanol). With the aid of the Ward and Torday equation the values of the diffusion coefficients of individual compounds and their equimolar mixtures were estimated. It was found that in the case of two types of investigated mixtures, i.e., HNAF + beta-diketone and HNAF + decanol the compound HNAF that was dominant in the mixed adsorbed monolayer and the more interfacially active also determined the kinetics of adsorption in mixed systems. In contrary to the mixture of two chelating reagents, in the case of a mixture of two solvating extractants the mixed system behaves like the less active, though dominant at the interface, reagent TBP. The same effect was observed in both of the considered diluents (toluene and octane). (c) 2005 Elsevier Inc. All rights reserved.
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页码:411 / 417
页数:7
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