Partition and water/oil adsorption of some surfactants.

Adsorption isotherms have been determined at the water/oil interface for five biphasic systems involving surfactants (non-ionic and ionic) present in both phases at partition equilibrium. The systems studied were polyoxyethylene(23)lauryl ether (Brij35) in water/hexane and four ionic surfactants, hexadecyltrimethylammonium bromide (CTAB), and a series of three tetraalkylammonium dodecylsulfate (TEADS, TPADS, and TBADS) in water/CH 2Cl 2. Interfacial tension measurements performed at the water/air and water/oil interfaces provided all the necessary information for the determination of the adsorption parameters by taking partition into account. These measurements also allowed the comparison of the adsorption properties at both interfaces which showed an increase of the adsorption equilibrium constant and a decrease of the maximum surface concentration at the water/oil interface compared to water/air. The values of the critical aggregation concentration showed, in all cases, that only the surfactant dissolved in the aqueous phase contribute to the decrease of the water/oil interfacial tension. In the case of the four ionic surfactants, the critical aggregation concentration obtained in biphasic conditions were lowered because of the formation of mixed surfactant-CH 2Cl 2 aggregates.

Association, partition, and surface activity in biphasic systems displaying relaxation oscillations.

Several biphasic systems giving rise to periodical Marangoni instability have been analyzed from the point of view of the physicochemical properties of the involved compounds. In each case, the compound at the origin of the oscillatory behavior has been identified: the reactant cetyltrimethylammonium bromide (CTAB) for the CTAB/picric acid (PH) system and the product of reaction dodecyl sulfate tetraalkylammonium (TAADS) for the sodium dodecyl sulfate/tetraalkylammonium bromide (SDS/TAAB) system. The properties of the latter system have been varied progressively by increasing the chain length of the tetraalkylammonium ion. Oscillations were observed whichever the direction of transfer (from water to dichloromethane and from dichloromethane to water). The comparison of the dynamic interfacial tension, recorded during transfer, to equilibrium measurements shows that the instability is favored when partition is highly in favor of the organic phase. The main criteria for the appearance of the instability are a high surface activity and a low interfacial adsorption.