The micellar and morphological properties of symmetric, cationic gemini surfactants have been well studied in the literature as a function of nature and type of the spacer group and the length and type of hydrophobic chain. In this paper, we have examined the effects of tail asymmetry on the properties of a series of cationic surfactants, the N-alkyl-1-N′-alkyl-2-N,N,N′,N′-tetramethyldiammonium dibromide. A novel synthetic method is used to prepare a series of these surfactants and the consequences of asymmetry on micellar properties are presented. This new method has been shown to be more efficient, with higher yields of the asymmetric surfactants than the yields of the accepted literature method. The critical micelle concentration values and the micelle sizes of the asymmetric gemini surfactants, 12-4-12, 12-4-10, 12-4-8, and 12-4-6 gemini surfactants, were obtained from conductivity and dynamic light scattering. With increasing chain asymmetry, the size of the micelle increased due to the formation of loose micelles. The addition of NaCl and Na2SO4 to the surfactant solutions increased the aggregate size, and this effect was more pronounced with increasing salt concentrations. These results are interpreted in terms of the effect these ions have on the “compactness” of the micelle structure.
Micellar properties of surface active ionic liquids: A comparison of 1-hexadecyl-3-methylimidazolium chloride with structurally related cationic surfactants
