Abstract

In this paper, the influence of Ca2+ on the flotation of a skarn type molybdenum ore and pure molybdenite mineral at pH 8 was studied using diesel as the collector. It was found that Ca2+ had little effect on molybdenum flotation at low concentrations. By further increasing Ca2+ concentration, the floatability of molybdenite—especially from the fine size fractions—was depressed even without the presence of fine gangue minerals. The mechanism responsible for the deleterious effect of Ca2+ on molybdenite flotation was studied by a range of techniques including zeta potential measurements, Scanning Electron Microscopy, and Energy Dispersive X-ray Spectrometer (SEM-EDS) analyses and molybdenum phase analyses. It was found that Ca2+ interacted with molybdenite edges producing CaMoO4 precipitates which were responsible for the depression of molybdenite flotation of Ca2+ by preventing the adsorption of diesel.

Highlights

  • Flotation exploits a difference in surface wettability on valuable and gangue minerals, and water quality has a significant impact on mineral flotation through the modification of surface wettability by ions in water [1,2,3,4]

  • It has been found that calcium ions can adsorb on molybdenite as a result of electrostatic interactions and increase the zeta potential of molybdenite or even reverse the zeta potential from negative to positive [11].Adsorbed calcium ions are attractive to negatively charged fine quartz or other gangue particles, deteriorating molybdenite flotation

  • This study indicates that the formation of CaMoO4 on molybdenum edges prevented the adsorption of diesel leading to the depression of molybdenum floatability

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Summary

Introduction

Flotation exploits a difference in surface wettability on valuable and gangue minerals, and water quality has a significant impact on mineral flotation through the modification of surface wettability by ions in water [1,2,3,4]. Due to the scarcity of fresh water and increasingly stringent regulations on the quality of discharged water, groundwater or sea water with a high strength of ions and recycled water are used by most flotation plants. This practice has resulted in an increase in ion strength of process water as a result of evaporation and ongoing ion inputs from groundwater (or seawater), chemicals added in flotation and run off from spoil [5,6,7]. The negative impact of calcium ions has been attributed to the bridging role of calcium ions which promote the coating of fine gangue (e.g., quartz) particles on molybdenite.

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