Kinetics of pressure-induced phase separation in polystyrene + acetone solutions at high pressures

The kinetics of pressure-induced phase separation in solutions of polystyrene (Mw = 129,200; PDI = 1.02) in acetone has been studied using time- and angle-resolved light scattering. A series of controlled pressure quench experiments with different quench depths were conducted at different polymer concentrations (4.0%, 5.0%, 8.2% and 11.4% by mass) to determine the binodal and spinodal boundaries and consequently the polymer critical concentration. The results show that the solution with a polymer concentration 11.4 wt% undergoes phase separation by spinodal decomposition mechanism for both the shallow and deep quenches as characterized by a maximum in the angular distribution of the scattered light intensity profiles. Phase separation in solutions at lower polymer concentrations (4.0, 5.0 and 8.2 wt%) proceeds by nucleation and growth mechanism for shallow quenches, but by spinodal decomposition for deeper quenches. These results have been used to map-out the metastable gap and identify the critical polymer concentration where the spinodal and binodal envelops merge. me scale of new phase formation and growth as (accessed) from the time evolution of scattered light intensities is observed to be relatively short. The late stage of phase separation is entered within seconds after a pressure quench is applied. For the systems undergoing spinodal decomposition, the characteristic wave number q m corresponding to the scattered light intensity maximum I m was analyzed by power–law scaling according to q m ∼ t − α and I m ∼ t β . The results show β ≈ 2 α . The domain size is observed to grow from 4 μm to 10 μm within 2 s for critical quench, but about 9 s for off-critical quenches. The domain growth displays elements of self-similarity.