The structure of polymerizable microemulsions containing styrene, dode
cyltrimethylammonium bromide, and brine is investigated by small-angle
neutron scattering (SANS) and quasielastic light scattering (QLS). SA
NS measurements suggest that these microemulsions consist of a unimoda
l population of swollen micelles that swell uniformly with the additio
n of styrene. The double exponential behavior of the autocorrelation f
unction measured with QLS experiments is attributed to collective and
self-diffusion modes. These modes appear in polydisperse systems at hi
gh volume fractions and are enhanced by repulsive interactions. The co
llective diffusion coefficient, which increases with added styrene and
decreases with salt, depends on both hydrodynamic and thermodynamic i
nteractions. The self-diffusion coefficient decreases monotonically wi
th added styrene. Adding salt does not affect the size of the swollen
micelles but does screen micelle interactions sufficiently that the co
ntribution to the autocorrelation function from self-diffusion disappe
ars. The experimental values characterizing hydrodynamic interactions
agree well with a recently developed theory for small charged spheres.