Lp. Novaki et al., FTIR and H-1 NMR studies of the solubilization of pure and aqueous 1,2-ethanediol in the reverse aggregates of aerosol-OT, LANGMUIR, 16(13), 2000, pp. 5573-5578
Solubilization of 1,2-ethanediol, ED, and its aqueous solution, ED-W, by th
e reverse aggregates of sodium bis(2-ethylhexyl) sulfosuccinate, Aerosol-OT
or AOT, in n-heptane and isooctane has been studied by FTIR and H-1 NMR. C
urve fitting of the v(OD) bands of the aggregate-solubilized (partially deu
terated) ED and ED-W showed the presence of a main peak and a smaller one.
The frequency of the former peak decreases, whereas its full width at half-
height increases as a function of increasing [solubilizate]/[AOT]. The depe
ndence on the later ratio of H-1 NMR chemical shifts, delta(proton), of sol
ubilized water, ED, ED-W as well as the surfactant discrete protons showed
monotonic increase or decrease. Results of both techniques indicated that E
D and/or water interact with the surfactant by a similar mechanism, i.e., b
y solvating its head-ions. The magnitudes of \Delta v(OD)\ and \Delta delta
(proton)\ showed, however, that AOT interacts more strongly with ED than wi
th water. Over the entire range of [solubilizate]/[surfactant], the main vo
n peak area corresponds to 85 +/- 2% (ED), and 88 +/- 2% (ED-W) of the tota
l peak area. These results show that the aggregate-solubilized ED or ED-W d
oes not seem to coexist in "layers" of different structures, as suggested b
y the multi-state water solubilization model.