The morphology of blends of polystyrene (PS) microgels with linear PS were
studied using NMR spectroscopy. Three techniques were employed to assess th
e intimacy of mirdng: isothermal;cross-polarization/magic angle-spinning (C
P/MAS) dipolar dephasing C-13 NMR, temperature-dependent 13C CP/ MAS NMR, a
nd one-pulse H-1 MAS NMR. The experimental data reveal that linear PS can p
enetrate: the core of soft microgels, whose network strands are substantial
ly larger than the linear chains. However when the microgel is highly cross
-linked, such penetration is prevented. These results are in accord with Fl
ory-Huggins swelling theory. Blends of linear PS with highly cross-linked m
icrogels yield thermodynamically stable morphologies, in which the componen
ts are molecularly dispersed, yet segmental contacts are virtually absent.
Such a phase morphology is novel and cannot be obtained with-conventional p
olymer blends.