Abstract

Surfactants of different kinds are important in the flotation of metal oxide ores. In this paper, a combined organic surfactant was formed through self-assembly of salicylhydroxamic acid (SHA) and isopropanolamine dodecylbenzenesulfonate (DBIA). The effects of SHA and DBIA on the flotation behavior of cassiterite were investigated. Density functional theory (DFT) calculations were used to clarify the microscopic adsorption mechanism of SHA and DBIA on the cassiterite surface. The flotation performance of the combined surfactant was investigated to determine the optimum ratio. Subsequently, the self-assembly behavior of the surfactants in aqueous solutions was examined using surface tension tests and molecular dynamics simulations. Flotation experiments and zeta potential, X-ray photoelectron spectroscopy (XPS), atomic force microscope (AFM), contact angle, and adsorption capacity analyses were used to explore the flotation behavior and adsorption mechanism at the solid–liquid–gas boundary. The maximum flotation recovery of cassiterite were 45.73 % and 71.25 % when SHA and DBIA were used alone. By contrast, with the developed combined surfactant, the flotation recovery at the same reagent concentration was 84.92 %. The SHA/DBIA surfactant co-adsorbed at the aqueous solution interface, which decreased the surface tension of the solution to 4.943 × 10−4 mol/L and resulted in formation of a stable foam layer. These effects altered the surface properties of cassiterite and enhanced its surface hydrophobicity. Overall, this study provides valuable mechanistic insights into the enhanced chelation complexation of self-assembled surface collectors with metal oxides.

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