Abstract

The effect of sodium salicylate (NaSal) additives on micellar structure and dynamics in aqueous solution of dodecyltrimethylammonium bromide (DTAB) has been studied by means of 1H-NMR and quasielastic neutron scattering (QENS) measurements. The molar ratio R (= C NaSal/ C DTAB) dependence on the peak shape of the NMR spectra revealed that a sphere-to-rod-like micellar transition took place around R=0.5. The chemical shift for the 1H atoms of the alkyl group of DTA + ion gave the information for the binding site of Sal − ion in micelles. The R dependence on the chemical shift for the aromatic group of Sal − ion clarified the selective binding feature of Sal − ion in micelles. The dynamic structure factor, S( Q, E), of the micellar molecules exhibited apparent broadening of the elastic scattering peak which was fitted well to a single Lorentzian function. The self-diffusion coefficient D was obtained from the Q-dependence of the HWHM of the Lorentzian function. The slope of D vs. R curve changed around the transition ratio ( R=0.5), reflecting the dynamic slowing down of the local relaxational motion of the micellar molecules in rod-like micelles.

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