The spontaneous fracture of polymer gels was studied. Contrary to crys
talline solids, where fracture usually happens instantaneously at a we
ll-defined breaking strength, the fracture of a polymer gel can occur
with a delay. When a constant force was applied, the cracks nucleated
and started to propagate after a delay that can be as long as 15 minut
es, depending on the force. This phenomenon can be understood by calcu
lating the activation energy for crack nucleation in arbitrary dimensi
on and accounting for the inhomogeneity of the gel network in terms of
its fractal dimension.