Interfacial tension of evaporating emulsion droplets containing amphiphilic block copolymers: Effects of solvent and polymer composition

Evaporating droplets of volatile organic solvent containing amphiphilic block copolymers may undergo hydrodynamic instabilities that lead to dispersal of copolymer micelles into the surrounding aqueous phase. As for related phenomena in reactive polymer blends and oil/water/surfactant systems, this process has been ascribed to a nearly vanishing or transiently negative interfacial tension between the water and solvent phases induced by adsorption of copolymer to the interface. In this report, we investigate the influence of the choice of organic solvent and polymer composition for a series of polystyrene-b-poly(ethylene oxide) (PS–PEO) diblock copolymers, by in situ micropipette tensiometry on evaporating emulsion drops. These measurements suggest that the sensitivity to the organic solvent chosen reflects both differences in the bare solvent/water interfacial tension as well as the propensity of the copolymer to aggregate within the organic phase. While instabilities coincident with an approach of the interfacial tension nearly to zero were observed only for copolymers with PEO content greater than 15 wt.%, beyond this point the interfacial behavior and critical concentration needed to trigger surface instability were found to depend only weakly on copolymer composition.

Nearly vanishing oil/water interfacial tensions induced by amphiphilic diblock copolymers drive interfacial instabilities and lead to dispersal of block copolymer micelles in water.Figure optionsDownload high-quality image (88 K)Download as PowerPoint slideHighlights
► Micropipette tensiometry to characterize interfacial behavior of amphiphilic copolymers within evaporating emulsion droplets.
► Instabilities coincident with an approach of interfacial tension nearly to zero.
► Interfacial tension and instabilities depend on solvent type and polymer composition.