This paper summarizes an extensive investigation of the thermodynamic
interactions that govern phase behavior in blends of polyolefins and e
xamines their relationship to pure component PVT properties. Interacti
on strengths, obtained by small-angle neutron scattering (SANS) measur
ements, were classified as regular or irregular according to their con
sistency with a solubility parameter formalism. Characteristic pressur
e P and temperature T* were obtained from PVT data on the pure compon
ents with various liquid-state models. For the regular blends, a close
correspondence was found between the SANS-based and PVT-based solubil
ity parameter assignments, the latter being closely related to P, as
expected. The pattern of deviations for the irregular blends, positive
in some and negative in others, effectively ruled out equation-of-sta
te contributions as a general explanation. However, the results sugges
t that mismatches in both P and T* play some role, and we offer some
tentative attempts at generalization.