Stress, strain, and optical birefringence were measured for a series of per
oxide-cured natural rubbers, having both isotropic and double network struc
tures. The residual stretch (permanent set) for the latter ranged from 2.0
to 4.5, with elastic moduli that were an increasing function of this residu
al strain, as found in previous works. A small birefringence, ca. 10(-5), w
as observed for the unstressed double networks, and its magnitude increased
with increasing residual strain. The sign of this birefringence correspond
ed to extension of the (undeformed) double networks. Under stress, the bire
fringence followed the stress optical law. The double network properties we
re interpreted using the constrained-chain model of rubber elasticity, with
the assumption of independent, additive contributions from the two compone
nt networks. The calculated results differed from the experimental findings
, in particular underestimating the residual strain. This failure is a cons
equence of the overprediction of the stresses during compression, a limitat
ion common to molecular theories of rubber elasticity. The modeling of the
double networks does account qualitatively for the sign of their unstressed
birefringence, which is due to the stress-optical coefficient being larger
in tension than in compression. This particular deviation from the stress-
optical law is known from both theory and experiment.