Shear modulus data are presented for a polyurethane system at differen
t stages of the gelation process. Data were collected over a wide freq
uency domain covering both the alpha relaxation and the internal mode
relaxation. At the gel point, both the loss modulus G '' and the stora
ge modulus G' have a power law frequency dependence over four decades
with an exponent 0.70 close to the value predicted by percolation theo
ry assuming Rouse dynamics. After the gel point G' exhibits a gel modu
lus which increases with increasing reaction extent, while G '' contin
ues to have a power law behaviour at low frequencies with an exponent
that decreases initially to 0.5 and then increases to 0.7 for the full
y grown gels. The presence of slow dynamical processes in gels is visi
ble in most reported dynamic mechanical measurements on different type
s of gels and is not expected by the standard model of polymeric gels.
A number of possible explanations are mentioned, but we conclude that
the slow dynamics in gels are at present an unexplained experimental
observation.