Sucrose monoalkanoates (SE) form microemulsions by mixing with lipophilic c
osurfactants such as the middle-chain alcohols, or sucrose polyalkanoates.
In the case that sucrose monododecanoate is combined with hexanol, a middle
-phase microemulsion is produced and coexists with excess water and oil pha
ses at optimum mixing fraction of SE and hexanol. The bicontinuous structur
e of the microemulsion was confirmed by means of self-diffusion coefficient
on NMR measurement.
A larger solubilization capability of oil is attained to a mixed mono- and
poly-dodecanoate system than that of the middle-chain alcohol. It is probab
ly due to the location of most of surfactant molecules at the micro-interfa
ce inside the microemulsion. In this system, instead of forming a three-pha
se region, a lamellar liquid crystal intrudes into multi-phase region since
the surfactant layer is rather rigid as which was supported by the results
of SAXS and ESR measurements. Further addition of a short-chain alcohol su
ch as propanol to the mixed system leads to the flexible interface, as a co
nsequence three-phase microemulsion with large solubilization is formed.