The diffusional properties in the cyclohexane/lecithin/water gel are invest
igated by means of quasielastic neutron scattering and depolarized light sc
attering. Also the pure organic solvent and sol phases of different composi
tions are investigated for a comparison. It is found that both translationa
l and rotational diffusion of water and lecithin are strongly correlated, a
nd become faster in the gel phase. This does not fit the current point of v
iew, where the rheological properties of the system are supposed to result
from the entanglement of giant linear micelles which grow up under addition
of water. As a further investigation, the aggregative phenomena occurring
in the system at the sol-gel transition are observed by means of a calorime
ter tao. Also in this case, the interpretation of the experimental data in
terms of the growth of linear giant aggregates leads to some inconsistencie
s. It is suggested that the macroscopic shear viscosity behavior can be tho
ught of as originated by a transient network determined by cooperative inte
rmicellar interactions, where the role played by water is not as simple as
assumed up to now. [S1063-651X(99)03401-7].