Abstract:Metal ions are widely present in flotation pulp. Metal ions change solution chemistry and mineral surface properties, consequently affecting mineral flotation. In this work, the effect of strontium ions on bastnaesite flotation with salicylhydroxamic acid (SHA) was investigated by microflotation tests, contact angle measurements, zeta-potential measurements, and X-ray photoelectron spectroscopy (XPS) analysis. Microflotation tests confirmed that the addition of strontium ions decreased bastnaesite floatability, compared with that in the absence of strontium ions. Contact angle measurements suggested that the pretreatment of strontium ions decreased SHA adsorption. Zeta potential measurements confirmed that the bastnaesite was depressed by the adsorption of positively charged strontium species, and the lower adsorption capacity of SHA onto the bastnaesite surfaces was obtained after modifying with strontium ions. XPS analysis demonstrated that strontium ions adsorbed onto the bastnaesite surfaces through the interaction between strontium ions and oxygen atoms of surface ≡ CeOH 0 groups. This occurrence hindered surface Ce sites which chelated with SHA and therefore, decreased bastnaesite floatability.

Ca 2+ , Mg 2+ , Sr 2+ and Fe 3+ were found to be commonly released into bastnaesite flotation pulp from minerals with relatively high concentrations. The influence and corresponding mechanism of Ca 2+ , Mg 2+ , Sr 2+ , Fe 3+ and Al 3+ , on bastnaesite flotation, have been studied by micro flotation tests, induction time measurements, adsorption measurements and solution chemistry analysis. It was found that all aforementioned metal ions depressed bastnaesite flotation. The order of depression ability was Fe 3+ > Al 3+ > Mg 2+ > Sr 2+ > Ca 2+ and the depression ability changed along with pH. The depression was mainly attributed to the adsorption of metals ions, which hindered collector adsorption. The species diagrams of metal ions changed along with pH, consequently changing the adsorption of metal ions on mineral surfaces, and therefore leading to different influences on flotation.

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In practical celestite flotation, iron contamination is commonly found on celestite surfaces. The effect of ferric ions on celestite flotation was assessed by a combination of ion release experiments, DFT calculation, X-ray photoelectron spectroscopy (XPS) analysis, adsorption isotherm study, and flotation experiments in this work. The ion release experiments showed that the associated limonite released ferric ions to solution. According to DFT calculation and surface complexation theory, we found that ≡SrOH0 and ≡SO4H0 are primary functional groups on celestite surface in aqueous environments. The XPS analysis and adsorption isotherm study revealed that ferric ions mainly adsorbed on celestite surface by complexing with two oxygen atoms of surface ≡SrOH0 groups to form ≡Sr–O–Fe–OH precipitates. Flotation results showed that ferric ions strongly depressed celestite flotation. Combined with the change in surface properties determined by XPS, it can be concluded that the adsorption of ferric ions on celestite surface decreased adsorption sites for the collector, and hence, led to depression on celestite flotation.