By means of a theoretical experiment it is demonstrated, that a barrier in the adsorption kinetics of a surfactant can be simulated by the presence of surface-active impurities. Hence, the application of models for the diffusion-kinetic-controlled and/or kinetic controlled adsorption presumes the proof of the surface chemical purity of the surfactant solution under investigation.Key words: Adsorption kinetics, model of diffusion-kinetic-controlled adsorption, effect of impurities on adsorption kinetics.Investigating~ the properties of surfactant adsorption layers the purity of the surfactant solutions used plays an important role. In particular the dynamic properties are strongly influenced by surface-active impurities [1][2][3]. In the evaluation of dynamic surface tension measurements of surfactant solutions in addition to the model of the diffusion-controlled adsorption [4,5] there are also applied models which take into consideration a special mechanism for describing the process of transferring the molecules from the state of solution to that of adsorption [5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21]. This paper is to demonstrate by means of a "theoretical" experiment "how surface-active impurities may effect the adsorption kinetic behaviour of surfactants and what kind of misinterpretation may be induced by their presence. The "theoretical" experiment shall be carried out in analogy with a practical one. The surface activity of the impurity is assumed to be stronger than that of the surfactant. The adsorption of the mixture of surface active compounds shall be described by a generalized Langmuir-isotherm.
roo-rl (t)-G (t)] (2)(c~-surface tension, cro-surface tension of pure water, R -gas constant, T-absolute temperature, t-time). Now we assume that the experimental findings are represented by such a dependence o (t), which -on its turn -is evaluated from the standpoint of adsorption kinetics. Furthermore as usually done in practice we assume that there will be no impurity in the surfactant solution under investigation. Then the model of the diffusion-kinetic-controlled adsorption [21,23] is used for the evaluation. Figure 1 represents the "experimental" dependence (e-e) as well as a family of curves cx (t) which relate to different kinetic constants of the model of diffusion-kinetic-controlled adsorption. These dependencies are analogous to the results which Borwankar and Wasan [21] obtained for the dynamic surface tension of n-decanoic acid solutions when applying a corresponding kinetic model to the experimental data given by Defay and Hommelen [24,25]. The experimental findings of [24,25] may lead to the conclusion of a hindered adsorption [21]. Just the same situation is met in the case of the above mentioned "theoretical" experiment, i. e. by the installation of an impurity in the surfactant solution system a hindered adsorption mechanism would be simulated for the true surfactant (main component).W527