Abstract
The aggregation of alkyltrimethylammonium surfactants &TA+ and ClsTA+ in dilute water solutions of sodium poly(styrenesu1fonate) has been investigated. Aggregation numbers were estimated with the time-resolved fluorescence quenching technique. In the calculations, results from binding isotherms and solubility measurements were used. Binding isotherms for dodecyltrimethylammonium bromide to the polyelectrolyte were determined using a surfactant-selective electrode. The aggregation numbers were found to be independent of the concentration of surfactant and type of counterion, but to increase with increasing surfactant tail length. From the kinetics of the quenching of pyrene fluorescence with hydrophobic and hydrophilic quenchers, it was concluded that compact aggregates with net negative charge were formed, in which the polyelectrolyte is intimately associated with the surfactant. The aggregates are joined by surfactant-free parta of the polyelectrolyte chain, the lengths of which depend on the amount of bound surfactant. The quencher dimethylbenzophenone was found to migrate between the aggregates at the highest concentration of the long-tailed surfactant.
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