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Mixing behaviour of charged and non-charged surfactants described by BET isotherms
Pierre Letellier1, Alain Mayaffre, Mireille Turmine
1Laboratoire Interfaces et Systèmes Electrochimiques, CNRS, UPR15-LISE, Université Pierre et Marie Curie-Paris6, Case 133, 4 place Jussieu, 75252 Paris Cedex 05, France.
Abstract:
We analysed various sets of published results concerning the mixing behaviour of charged and non-charged surfactants, beyond their aggregation threshold, by means of the BET model modified by Stokes and Robinson. This approach, which is mainly used to account for properties of concentrated aqueous salt solutions, provides a good description of the properties of mixed micelles across the complete scale of compositions between the two pure surfactants. We use analyses of the behaviour of several systems reported in the literature for illustration. We consider the significance of the parameters C and r introduced in the BET model. For mixed micelle solutions in the presence of a support electrolyte, the value of the solvation enthalpy of the charged amphiphile by the non-ionic surfactant is small (C close to one). This model is compared to the regular solution theory (RST).
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A solution is a homogeneous mixture composed of a solvent, the major component, and a solute, the minor component. The physical state of a solution—solid, liquid, or gas—is typically the same as that of the solvent. Solute concentrations are often described with qualitative terms such as dilute (of relatively low concentration) and concentrated (of relatively high concentration).
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