The viscosity of a water-rich microemulsion phase composed of C(12)E(5
), water, and decane has been measured. Attention has been focused on
the concentration dependence of the viscosity along the emulsification
failure boundary, where the microstructure of the system is that of o
il-swollen spherical micelles. At high dilution, the concentration dep
endence of the relative viscosity is consistent with the behavior of a
suspension of spheres, with an effective micellar size characterized
by its hydrodynamic radius. At higher concentrations, where interactio
ns are important, a good correlation with colloidal hard-sphere system
s is obtained if the apparent micellar size is characterized by the ha
rd-sphere radius. With increasing temperature away from the emulsifica
tion failure boundary, a significant increase in the viscosity is obse
rved. The observed temperature dependence of the viscosity correlates
with results obtained previously from H-2 NMR relaxation and self-diff
usion experiments and is consistent with a micellar growth with increa
sing temperature.