Pressure- and Temperature-Induced Association of Arborescent Polystyrene-graft-poly(ethylene oxide) Copolymers at the Air−Water Interface

Abstract

The influence of surface pressure and subphase temperature on the association of arborescent polystyrene- graft-poly(ethylene oxide) (PS- g-PEO) copolymers at the air-water interface was investigated using the Langmuir balance and atomic force microscopy (AFM) techniques. These dendritic molecules form stable condensed monolayers with surface compressional moduli >250 mN/m. The variation in film thickness observed as a function of surface pressure suggests that at low surface pressures (gaslike phase) the PEO chains remain adsorbed at the air-water interface. At higher surface pressures (condensed phase), the PEO chains partially desorb into the subphase and adopt a more brushlike conformation. Large islandlike clusters with a broad size distribution were observed for samples with PEO contents of up to 15% by weight. In contrast, copolymers with PEO contents of 22-43% displayed enhanced side-by-side association into ribbonlike superstructures upon compression. The same effect was observed even in the absence of compression when the subphase temperature was increased from 12 to 27 degrees C. The temperature-induced association was attributed to increased van der Waals attractive forces between the PS cores relative to the steric repulsive forces between PEO chains in the coronas because the solvent quality for the PEO segments decreased at higher temperatures. The restricted number of superstructures observed for arborescent copolymers as compared with linear- and star-branched PS-PEO block copolymers is attributed to the enhanced structural rigidity of the molecules due to branching.