A simple and rapid method for the determination of the surface equations of state and adsorption isotherms for efficient surfactants
Catherine D. Taylor, Dimitrina S. Valkovska, Colin D. Bain
Abstract
Catherine D. Taylor, Dimitrina S. Valkovska, Colin D. Bain
Abstract
A simple and fast method for determination of adsorption isotherms for highly surface-active surfactants is presented. Efficient surfactants often have critical micelle concentrations <0.1 mM and the determination of surface tension isotherms involves measurements at very low bulk concentrations where long equilibration times, solution depletion and trace impurities can seriously compromise accuracy. In the method described here, a bubble of known surface area, A1, and surface excess concentration, Γ1, is expanded rapidly to a new surface area, A2. The surface tension at the new surface excess, Γ2 = Γ1A1/A2, is evaluated by extrapolation of the surface tension relaxation profile to t = 0. It is shown empirically that the choice of t = 0 to correct for adsorption of the surfactant to the growing bubble is ⅔ of the bubble growth time. The equation of state σ(Γ) when combined with equilibrium surface tension measurements in the vicinity of the c.m.c. is sufficient to define completely the adsorption isotherm. This method is then applied to the determination of the adsorption isotherms of the non-ionic surfactants C12E5 and C12E3 and the cationic surfactant C16TAB in the presence of 0.1 M NaBr.
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A simple and fast method for determination of adsorption isotherms for highly surface-active surfactants is presented. Efficient surfactants often have critical micelle concentrations <0.1 mM and the determination of surface tension isotherms involves measurements at very low bulk concentrations where long equilibration times, solution depletion and trace impurities can seriously compromise accuracy. In the method described here, a bubble of known surface area, A1, and surface excess concentration, Γ1, is expanded rapidly to a new surface area, A2. The surface tension at the new surface excess, Γ2 = Γ1A1/A2, is evaluated by extrapolation of the surface tension relaxation profile to t = 0. It is shown empirically that the choice of t = 0 to correct for adsorption of the surfactant to the growing bubble is ⅔ of the bubble growth time. The equation of state σ(Γ) when combined with equilibrium surface tension measurements in the vicinity of the c.m.c. is sufficient to define completely the adsorption isotherm. This method is then applied to the determination of the adsorption isotherms of the non-ionic surfactants C12E5 and C12E3 and the cationic surfactant C16TAB in the presence of 0.1 M NaBr.
Key concepts: Surface tension, Pulmonary surfactant, Adsorption, Maximum bubble pressure method, Gibbs isotherm, Chemistry, Bubble, Extrapolation