Phase behaviour of poly(vinyl methyl ether)‐cross‐polystyrene semi‐interpenetrating networks

Abstract

AbstractSemi‐interpenetrating polymer networks of varying composition are prepared by crosslinking polystyrene containing a small number of maleic anhydride groups (4.8 mol% of MA units) with hexamethylene‐diamine (HMDA) in the presence of linear poly(vinyl methyl ether) (PVME). Lightly crosslinked samples are homogeneous at room temperature and show a phase behaviour similar to uncrosslinked blends, i.e. lower critical solution temperature (LCST) behaviour. The influence of crosslinking on the phase behaviour has been studied by small angle light scattering (SALS) and turbidity measurements. The cloud point strongly depends on the heating rate. The presence of the network reduces the stable single phase region in agreement to theory. In systems showing spinodal decomposition, it is expected that some concentration fluctuations will grow more rapidly than others resulting in a separated phase system which shows high degree of connectivity with characteristic dimensions. Using temperature jump experiments, SALS can be used to estimate parameters of the phase separation kinetics and the characteristic dimensions of the phases. In temperature jump experiments into the spinodal region a maximum in the scattered light intensity is observed with time at a certain scattering vector. However, the semi‐IPN's develop no scattering maximum. This is explained by a damping of the thermodynamical dominant wavelength in spinodal decomposition in the network.