Plots of the temperature dependence of the shear viscosity η of
C12E5/D2O mixtures with
compositions
in the range 0.60 × 10-2 < y <
10.08 × 10-2 (critical composition
y
c = 1.08 × 10-2;
y, mass fraction of
C12E5)
are S-formed (a shallow minimum at a lower temperature
T
η
,min and a maximum at a higher
temperature
T
η
,max). The measurements are
carried out in the temperature range 5 °C < T <
T
P; T
P ≈ 30 °C
approaching
the lower part of the binodal curve (T
P,
temperature of phase separation of the mixture). In the
temperature
range (T
P −
T
η
,max) the viscosity decreases
with increasing temperatures. At compositions y < 0.60
× 10-2
the viscosity decreases with increasing temperature monotonically.
The self-diffusion coefficient of
C12E5
in C12E5/D2O mixtures is measured
in the same temperature and composition range. The findings of
both
types of experiments are rationalized in terms of a model developed by
Nilsson et al. (J. Phys. Chem.
1983,
87, 1377). The results give support to the hypothesis that
the characteristic features of the temperature
and composition dependence of both transport coefficients in the large
aggregate region of the phase
diagram have a common cause: The structural dynamics of the large
micellar aggregates increases
approaching the liquid/liquid coexistence curve at compositions
y > y
c. Concentration
fluctuations with
long range correlations appear to be involved in this
process.