4.7 Article

A fundamental assessment of the impacts of cation (Cd, Co, Fe) substitution on the molecular chemistry and surface reactivity of sphalerite

Journal

MINERALS ENGINEERING
Volume 160, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.mineng.2020.106695

Keywords

Sphalerite flotation; Surface chemistry; Mineral chemistry; Collectors; Raman; Band gap

Funding

  1. DST-NRF-CIMERA
  2. Society of Economic Geologists (SEG)

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A series of sphalerite mineral samples substituted with cadmium, cobalt, and iron were synthesized to investigate the impact of cation substitution on the crystal structure, bonding environment, and electronic properties of sphalerite. Results from XRD, Raman, and zeta potential experiments showed that cation substitution altered the lattice distortions, introduced new metal-sulfur bonds, and changed the band gap of sphalerite. These alterations influenced the electrokinetic response of sphalerite in flotation conditions, with cobalt-bearing samples having the most notable effect on zeta potential measurements.
A series of cadmium-, cobalt-, and iron-substituted (0-4 wt%) sphalerite mineral samples were synthesised to test how the presence of these cation substituents alter the crystal structure, surface bonding environment and electronic properties of sphalerite and to illustrate how these alterations impact the electrokinetic behaviour of mineral surfaces under conditions relevant to sphalerite flotation. A combination of X-ray Diffraction (XRD), Raman and ultraviolet-visible spectroscopies, and zeta potential experiments were used to demonstrate these impacts. XRD results showed a positive correlation between the measured lattice distortions and the ionic size and concentration of the respective cation substituents. Raman results confirmed the presence of new metal-sulphur (M-S) bonds within the ZnS host cluster reflected by a new impurity mode which correlates to the concentration and chemical nature of the cation substituents. The presence of metal substituents further induced a change in the band gap of sphalerite which reduced according to Cd > Fe > Co. These measurements informed the effect of the molecular characteristics of impurity-bearing sphalerite on the electrokinetic response of sphalerite in the presence of CuSO4 and xanthate collector. Cobalt-bearing sphalerites which have the lowest band gap and greatest distortions to molecular and crystal structure had the most notable impact on zeta potential measurements. A small increase in Co concentration induced a larger shift in point of zero charge for collectorless activation but did not impact the collector interactions. Conversely, Cd which has a wider band gap is less electronegative than Co exhibited the reverse behaviour. This study thus details how the presence of cation substituents modifies sphalerite bulk structure, in turn impacting its surface bonding environment and electronic properties, and ultimately exerting a notable control on flotation chemistry.

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