An
experimental study is presented for the reverse micellar system
of 15% by mass polydisperse hexaethylene glycol monodecylether (C10E6) in cyclohexane with varying amounts of added
water up to 4% by mass. Measurements of viscosity and self-diffusion
coefficients were taken as a function of temperature between 10 and
45 °C at varying sample water loads but fixed C10E6/cyclohexane composition. The results were used to inspect
the validity of the Stokes–Einstein equation for this system.
Unreasonably small reverse average micelle radii and aggregation numbers
were obtained with the Stokes–Einstein equation, but reasonable
values for these quantities were obtained using the ratio of surfactant-to-cyclohexane
self-diffusion coefficients. While bulk viscosity increased with increasing
water load, a concurrent expected decrease of self-diffusion coefficient
was only observed for the surfactant and water but not for cyclohexane,
which showed independence of water load. Moreover, a spread of self-diffusion
coefficients was observed for the protons associated with the ethylene
oxide repeat unit in samples with polydisperse C10E6 but not in a sample with monodisperse C10E6. These findings were interpreted by the presence of reverse
micelle to reverse micelle hopping motions that with higher water
load become increasingly selective toward C10E6 molecules with short ethylene oxide repeat units, while those with
long ethylene oxide repeat units remain trapped within the reverse
micelle because of the increased hydrogen bonding interactions with
the water inside the growing core of the reverse micelle. Despite
the observed breakdown of the Stokes–Einstein equation, the
temperature dependence of the viscosities and self-diffusion coefficients
was found to follow Arrhenius behavior over the investigated range
of temperatures.