M. Gradzielski et al., INVESTIGATIONS ON L(2) PHASE AND CUBIC PHASE IN THE SYSTEM AOT 1-OCTANOL WATER, Journal of colloid and interface science, 169(1), 1995, pp. 103-118
The properties of L(2) phase and cubic phase in the ternary system AOT
/1-octanol/water have been studied by means of electrical conductivity
, NMR self-diffusion experiments, theology, static and dynamic light s
cattering, SANS, and DSC. L(2) phase and cubic phase are neighboring p
hases that are both isotropic but vary largely with respect to their m
acroscopic appearance; i.e., the L(2) phase is of low viscosity, where
as the cubic phase is gel-like. At the phase transition, L(2) phase --
> cubic phase, no discontinuities were observed for the electrical con
ductivity and the self-diffusion coefficient of water; i.e., both phas
es should structurally be closely related and both are bicontinuous. S
ANS showed that in the cubic phase the size of the structural units de
creases with increasing AOT concentration. The self-diffusion coeffici
ents of both water and octanol/amphiphile are decreasing in parallel w
ith the size of the structural units. At the same time the shear modul
us rises with increasing surfactant concentration, which can be explai
ned in terms of a simple network theory, where each structural unit ac
ts as a network point. At high temperatures the cubic phase melts to f
orm the L(2) phase with transition enthalpies of typically 5-250 mJ/g.
Finally, it was observed that for not too high AOT content such a pha
se transition occurs also upon lowering the temperatures; i.e., a reve
rse melting transition takes place. (C) 1995 Academic Press, Inc.