Jarosite, beudantite and alunite are members of the alunite supergroup. Minerals like those have been detected in different environments on Earth. These jarosite-type compounds are common in acid rock drainage environments and acid sulfate soils, resulting from the weathering of sulfide ores; they are also present in bioleaching systems because they are found in cultures of iron-oxidizing microorganisms. Jarosite is also generated in hydrometallurgical circuits, mainly in zinc hydrometallurgy. These minerals can be used to immobilize different elements such as arsenic and lead, among others. Jarosite and alunite have also been detected on the surface of Mars; the presence of jarosite and alunite and other sulfates provides evidence for the existence of water on Mars. In this work, an exhaustive review of the natural formation, synthesis, structure, thermodynamics, and reactivity of jarosite, beudantite and alunite are included. The capacity of jarosites for the immobilization of the elements, such as lead and arsenic, and information about studies related to jarosite formation on Mars are also included.

An option to improve the leaching efficiency of chalcopyrite is pretreatment prior to leaching. Pretreatment variables, such as the curing time and the addition of chloride, can increase the kinetics of copper extraction, particularly for sulphide ores. However, there has been little research on the topic. The reactions that govern this phenomenon have not been clearly identified. In this study, the effects of sulphuric acid and sodium chloride agglomeration and curing on chalcopyrite leaching were evaluated at various temperatures: 25, 50, 70, and 90 °C. The pretreated ore and leach residues were characterised by X-ray diffraction, scanning electron microscopy, and reflected light microscopy. Under the conditions of 15 kg/t of H₂SO₄, 25 kg/t of NaCl, and 15 days of curing time (as pretreatment), the following products were identified: CuSO₄, NaFe₃(SO₄)₂(OH)₆, Cu₂Cl(OH), and S⁰. Increasing the curing time and leaching temperature increased copper leaching. The copper extraction was 94% when leaching at 90 °C after pretreatment with 50 g/L of Cl⁻ and 0.2 M of H₂SO₄. Elemental sulphur, jarosite, and copper polysulphide (CuS₂) were detected in the leaching residues.

Thiosulfate effluents are generated in the photography and radiography industrial sectors, and in a plant in which thiosulfates are used to recover the gold and silver contained in ores. Similar effluents also containing thiosulfate are those generated from the petrochemical, pharmaceutical and pigment sectors. In the future, the amounts of these effluents may increase, particularly if the cyanides used in the extraction of gold and silver from ores are substituted by thiosulfates, or if the same happens to electronic scrap or in metallic coating processes. This paper reports a study of the oxidation of thiosulfate, with oxygen using copper (II) as a catalyst, at a pH between 4 and 5. The basic idea is to avoid the formation of tetrathionate and polythionate, transforming the thiosulfate into sulfate. The nature of the reaction and a kinetic study of thiosulfate transformation, by reaction with oxygen and Cu²⁺ at a ppm level, are determined and reported. The best conditions were obtained at 60 °C, pH 5, with an initial concentration of copper of 53 ppm and an oxygen pressure of 1 atm. Under these conditions, the thiosulfate concentration was reduced from 1 g·L⁻¹ to less than 20 ppm in less than three hours.

The dissolution of copper sulphide ores continues to be a challenge for the copper industry. Several media and leaching alternatives have been proposed to improve the dissolution of these minerals, especially for the leaching of chalcopyrite. Among the alternatives, pretreatment prior to leaching was proposed as an option that increases the dissolution of copper from sulphide ores. In this study, a mineral sample from a copper mining company was used. The copper grade of the sample was 0.79%, and its main contributor was chalcopyrite (84%). The effect of curing time (as pretreatment) in a chloride media on copper sulphide ore was evaluated at various temperatures: 25, 50, 70 and 90 °C. The pretreated sample and leaching residues were characterized by X-ray diffraction, scanning electron microscopy, and reflected light microscopy. Pretreatment products such as CuSO₄, NaFe₃(SO₄)₂(OH)₆, and S⁰ were identified although with difficulty, due to the low presence of chalcopyrite in the initial sample (1.99%). Under the conditions of 15 kg/t of H₂SO₄, 25 kg/t of NaCl, and 15 days of curing time, a copper extraction of 93.1% was obtained at 90 °C with 50 g/L of Cl⁻ and 0.2 M of H₂SO₄.

Jarosite, beudantite, and alunite are members of the alunite supergroup