Effects of hydrophobic/hydrophilic blocks ratio on PS-b-PAA self-assembly in solutions, in emulsions, and at the interfaces

Abstract

Composite organized molecular assemblies of amphiphilic block copolymers exhibit various properties and functionalities and have attracted much attention recently. Many research studies have focused on adjusting these properties by varying the fabrication approach and by controlling the morphology of the aggregates. This work involved an investigation of the self-assembly behavior of a series of polystyrene-b-polyacrylic acid (PS-b-PAA) homologues with different block ratios in water-in-oil (W/O) and oil-in-water (O/W) emulsions. These emulsions simultaneously formed via a spontaneous emulsification process across the liquid/liquid interface. A variety of aggregates of the polymers with metal ions were obtained, including microcapsules, spherical micelles, rod-like and disc-like micelles, vesicles, and interior microphase-separated particles. These structures formed either in the emulsion droplets or in the continuous phase, and then proceeded to adsorb at the air/liquid interface or the planar liquid/liquid interface to form thin films. The influence of the molecular structure, the concentration of the metal ions, and the nature of the metal ion on the self-assembly behavior of the polymer molecules and the aggregate morphologies is discussed. In addition, these composite structures are shown to exhibit higher catalytic activity and good stability for the hydrogenation of nitroarenes in aqueous solutions.