Abstract

The recovery of difficult-to-float coal using traditional nonpolar hydrocarbon oil collectors can be challenging, particularly for low-rank or oxidized coal. Thus, there is a need for more efficient flotation agents. Nanoparticle flotation collector technology has become increasingly popular in the field of mineral processing, and the presence of various ions in the slurry can significantly affect the interaction between collectors and mineral surfaces. In this study, cationic polystyrene (PS) nanoparticles were prepared using an emulsion polymerization method, and the effects of Na+ ion concentration on the in situ adsorption and desorption processes, adsorption layer configuration, and adsorption kinetics of PS particles on amorphous carbon (coal model) and SiO2 sensors (quartz mineral model) were analyzed using the quartz crystal microbalance with dissipation (QCM-D) technique. Our results showed that the hydrophobic PS nanoparticles irreversibly adsorbed onto both amorphous carbon and SiO2 sensors under different environmental conditions, and their adsorption capacity decreased gradually with increasing Na+ ion concentration. Increasing Na+ ion concentration from 0 M to 1.0 M resulted in a 24.4% and 30.9% decrease in equilibrium adsorption capacities of PS nanoparticles onto amorphous carbon and SiO2 surfaces, respectively. The adsorption rate of PS nanoparticles onto the SiO2 surface was much greater than that on the amorphous carbon surface. The adsorption rate constant of PS nanoparticles onto SiO2 surfaces was 0.782 at 0.1 M Na+ ion concentration, while its adsorption rate constant onto amorphous carbon surfaces was only 0.060. Moreover, the adsorption process was found to be more in line with the quasi-primary kinetic model. These findings suggest that PS nanoparticles may serve as promising flotation collectors for the recovery of difficult-to-float coal, and highlight the importance of considering the effect of dissolved ions on the adsorption properties of flotation collectors.

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