Monolayer firms of PS-b-PEO diblock copolymers at the air/water- and an oil/water-interface

Amphiphilic diblock copolymers consisting of a hydrophobic polystyrene block (PS) and a hydrophilic poly(ethylene oxide) block (PEO) with block sizes of 1000 or 3000 g/mol for both blocks were studied at the air/water and toluene:water interface. Measurements of the film pressure pi of spread monolayers at the water surface reveal two limiting regimes of the pi - a(m) isotherms, in which the mean molecular area a(m) is determined either by the size of the hydrophilic or the hydrophobic blocks of the PS-PEO molecules. The interfacial activity of the block copolymers at the toluene/water interface was studied by measuring the interfacial tension a over a wide range of concentrations. Pronounced differences in the temperature dependence of the interfacial tension were observed, depending mostly on the block length of the hydrophilic PEO block. From the temperature dependence of sigma it is inferred that for the block copolymers with the PEO block size of 3000 g/mol the phase inversion temperature (PIT) is well above 60 degrees C while for those with a PEO block size of 1000 g/mol the PIT is below or near 25 degrees C in the toluene/water system.