Ech. To et al., Excess chemical potentials, excess partial molar enthalpies, entropies, volumes, and isobaric thermal expansivities of aqueous glycerol at 25 degreesC, J SOL CHEM, 28(10), 1999, pp. 1137-1157
The vapor pressures p the excess partial molar enthalpies of glycerol He,,
the densities d and the thermal expansivities oc, of aqueous glycerol were
measured at 25 degrees C. From the vapor pressure data, the excess chemical
potential of H2O mu(W)(E) was calculated, assuming that the partial pressu
re of glycerol Poly is negligibly small. The excess chemical potential of g
lycerol mu(Gly)(E) was estimated by applying the Gibbs-Duhem relation and t
hese data were used to calculate the excess partial molar entropies S-Gly(E
). From the density data, the excess partial molar volumes of glycerol V-Gl
y(E) and from the thermal expansivity data, the normalized cross fluctuatio
ns (SV)Delta, introduced by us earlier, were evaluated. While the detailed
manner in which glycerol modifies the molecular arrangement of H2O in its i
mmediate vicinity is yet to be elucidated, the hydrogen bond probability in
the bulk H2O away from solute molecules is reduced gradually as the glycer
ol composition increases to the point where putative presence of icelike pa
tches is no longer possible. Thereupon, a qualitatively different mixing sc
heme seems to set in.