Relating Nanoparticle Shape and Adhesiveness to Performance as Flotation Collectors

Abstract

Cationic polystyrene-core-poly­(<i>n</i>-butyl methacrylate)-shell (PS–PB) nanoparticles perform as flotation collectors as they spontaneously adsorb onto 43 μm glass beads in water, promoting glass bead attachment to air bubbles. Under our flotation conditions at room temperature, polystyrene is a hard plastic, whereas, with glass transition near room temperature, poly­(<i>n</i>-butyl methacrylate) is a soft polymer. Colloidal probe atomic force microscopy measurements revealed that the pull-off forces and the work of adhesion of PS–PB nanoparticles to glass were significantly higher than observed with harder PS particles. Glass bead recovery in laboratory flotation experiments increased significantly with thickness of the soft PB shells on the PB–PS core/shell nanoparticles. Ninety-two nm Janus particles consisting of one PS and one PB lobe were also very effective collectors. We propose that high nanoparticle/glass bead adhesion minimizes nanoparticle removal by bead/bead collisions (nanoscale ball milling) during mixing and flotation