Fractional precipitation of copiapite-halotrichite efflorescent salts on AuCu mine tailings under semi-arid climates in northern Chile

The oxidation of pyrite involves a series of chemical reactions that, depending on climatic conditions, can give rise to different mineral phases and morphologies. When oxidation takes place in semi-arid climate, the development of efflorescent salts on the surface of mine tailings is characteristic. These salts are mainly composed of Fe, Al and Mg sulfates and may accumulate valuable metals liberated through the dissolution of tailing minerals.

This research aims to describe the evolution of salt precipitation from the economic and environmental perspective. For this purpose, we sampled efflorescent salts formed during the summer season on the surface of a tailing impoundment located in the north of Chile. The materials underwent comprehensive characterization utilizing X-ray techniques and scanning electron microscopy.

The findings reveal a fractional precipitation in the crystallized salts. In an advanced oxidation system, characterized by multiple seasons of crystallization, dissolution and oxidation, the dry season begins with the precipitation of sulfates from a highly acidic solution dominated by Fe³⁺. This solution results from the dissolution and oxidation of the previous season sulfates. This initial stage is characterized by the presence of jarosite and gypsum, which are subsequently replaced by ferricopiapite. Towards the progress of the dry season, copiapite becomes more magnesian and precipitates alongside coquimbite and alunogen. Finally, halotrichite and pickeringite begin to crystallize. Base metal cations such as Co, Cu, Mn, Ni and Zn are preferentially incorporated into halotrichite-pickeringite sulfates during the most advanced evaporation phase.