Polystyrene blend with poly , thin film

Surface-directed spinodal decomposition was first observed in an isotopic polymer blend (Jones et al. 1991) thin films of a mixture of poly(ethylene-propylene) and its deuterated analogue were annealed below the upper critical solution temperature and the depth profiles measured using forward recoil spectrometry, to reveal oscillatory profiles similar to those sketched in figure 5.30. Similar results have now been obtained for a number of other polymer blends, including polystyrene with partially brominated polyst)u-ene (Bruder and Brenn 1992), polystyrene with poly(a-methyl styrene) (Geoghegan et al. 1995) and polystyrene with tetramethylbisphenol-A polycarbonate (Kim et al. 1994), suggesting that the phenomenon is rather general. 

Thin films of blended deuterated polystyrene (dPS) and poly(vinyl methyl ether) (PVME) were imaged as a fimction of the dPS PVME ratio. Near the critical composition of 35% dPS, an imdulating, spinodal-like structure was observed, whereas for compositions away from the critical mixture ratio, regular mounds or holes (< dPS < < crit and < dPS > (pent, respectively) were present. These variations were assigned to surface tension effects (120). Blends of PBD, SBR, isobutylene-brominated p-methylstyrene, PP, PE, natural rubber, and isoprene-styrene-isoprene block rubbers were imaged (Fig. 18). Stiff, styrenic phases and rubbery core-shell phases were evident as the authors utilized force-modulated afm to determine detailed microstructure of blends, including those with fillers such as carbon-black and silica (121). 

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