Langmuir, Vol.21, No.7, 2682-2688, 2005
Zwitterionic heterogemini surfactants containing ammonium and carboxylate headgroups. 1. Adsorption and micellization
Zwitterionic heterogemini surfactants with two hydrocarbon chains and two different hydrophilic groups, N,N-dimethyl-N-[2-(N '-alkyl-N '-beta-carboxypropanoylamino)ethyl]-1-alkylammonium. bromides (2C(n)AmCa, where n represents the hydrocarbon chain lengths of 8, 10, 12, and 14), were synthesized by N V-dimethylethylenediamine with alkyl bromide, followed by reaction with succinic anhydride. One of the hydrophilic groups is a carboxylate anion, and the other is an ammonium cation. Their physicochemical properties were characterized by measuring equilibrium and dynamic surface tension, fluorescence intensity of pyrene, and light-scattering intensity. A relationship between a logarithm of critical micelle concentration (cmc) and hydrocarbon chain length showed a linear decrease upon increasing chain length and then a departure from linearity at n = 14. This is due to the existence of premicellar aggregations at concentrations below the cmc for n = 14. The surface tension of 2CnAmCa reached 27-30 mN m(-1) at each cmc, indicating efficiencies typical of hydrocarbon chain surfactants. The adsorbing rate at the air/water interface became slow with an increase of the chain length. From the fluorescence intensity ratios of 373 and 384 mn using pyrene as a probe, for n = 8, 10, and 14, the pyrene was solubilized in surfactant micelles at around the cmc, whereas for n = 12 the pyrene was solubilized from a concentration of 10-fold the cmc. The scattering intensities by dynamic light scattering also increased from around these concentrations for each chain length, showing the formation of aggregates in solution.