The swelling in common (benzene) and selective (CCl4) solvents and small an
gle X-ray scattering (SAXS) of interpenetrating polymer networks (IPNs) of
PPO/PMMA in all composition intervals are studied. It is shown that in both
solvents IPNs swell better than the pure crosslinked polymers; that may be
caused by a smaller degree of crosslinking of each component in IPN in com
parison with the crosslinking of pure polymers. This leads to lower network
density in IPNs than in the networks of pure polymers. The unusual effect
is found: the IPN enriched with PMMA has the maximum swelling in CCl4, wher
eas PMMA itself does not swell in this solvent. SAXS measurements show that
ordering in IPNs, i.e. microphase separation (MPS), is absent, but there a
re structural heterogeneities in the initial dry state of IPNs which are ty
pical for these systems. These heterogeneities grow after swelling in a sel
ective solvent. We suggest that PMMA units cluster together in poor solvent
and as a result the internal stresses arise during swelling, which causes
the large swelling of IPNs in selective solvent. the structure of the asymm
etrical IPNs does not change with temperatures increasing up to 95 degrees
C and dropping down to room temperature; as a consequence, the equilibrium
swelling is also insensitive to the temperature. On the contrary, the struc
ture of symmetrical IPNs changes with heating and comes back very slowly by
returning to room temperature. (C) 2000 Elsevier Science Ltd. All rights r
eserved.