The assessment of mineral surface hydrophobicity at the industrial scale is a challenge. In some industrial situations, such information is indirectly obtained from other proxy variables. A well-known example of this is observed in the Cu-Mo selective flotation operation, where sodium hydrosulphide is used to change the redox potential and, controlling this value, determine when Cu-sulphide floatability is inhibited. Preliminary experiments indicate that this reagent may also promote the formation of solid precipitates, reducing its impact on the redox potential. This study aims at designing a simple strategy at the laboratory scale to report and quantify NaSH losses due to parallel, irreversible, and/or fast reactions, such as precipitation. Experiments carried out using process water coming from a Cu-Mo selective flotation plant in Chile show that departing from different pH conditions and the addition of hydrosulphide ions effectively triggers the precipitation of specific metal ions, decreasing its availability to reduce the redox potential of the aqueous solution. For this specific case scenario and water quality, around 5% of the NaSH dosed precipitated. An SEM-EDX analysis of the produced solid phase shows that it is composed of mainly iron sulphide and hydroxide, along with other metal hydroxides. More importantly, it was found that dosing the reagent at the same concentration, but in the form of small increments, allows reaching the redox potential more efficiently, reducing to some extent the precipitate production and the unnecessary NaSH consumption in up to 30% of the NaSH dosed. Preliminary 1-D modelling of the process, based on mass transport coupled with reaction mechanisms, provided a first indication of the best dosing conditions for this reagent. The latter is expected to contribute to the development of better and improved reagent dosage technologies in froth flotation environments.

The presence of arsenic-bearing minerals in ores, notably enargite (${Cu}_{3}As{S}_4$), remains an unresolved issue for copper beneficiation processes, including those for porphyry copper deposits. In particular, several operational challenges remain for the selective flotation of enargite from copper–sulphide ores, as well as the selective leaching of arsenic from enargite in copper concentrates. This study addresses these challenges from the standpoint of mediator science, where structures with specific elemental compositions observed by several authors at the surface of enargite and chalcopyrite, under different conditions and analytical techniques, are compiled and analysed. Most probable surface species, observed using technologies measuring the outmost surface layer and occurring onto the mentioned minerals, are identified and compared to species predicted by classic thermodynamic calculations. The results indicate that for chalcopyrite the major species formed in acidic conditions is elemental sulphur, while copper oxide and iron oxides and oxy-hydroxides species predominate with increasing pH. For the case of enargite, a similar situation is observed at low pH values, although slightly acidic conditions appear as a less examined condition for this mineral. Some of the observed species were found to be consistent with thermodynamic predictions, while others are notably absent. Particularly, for the case of enargite researchers have reported the formation of arsenic (III) oxide at pH values as high as 13, and observation not predicted by Pourbaix diagrams. Thus As₂O₃ could be considered a metastable species at highly alkaline conditions, which opens an option to beneficiation from froth flotation. Interestingly, at the same pH condition, iron oxide and oxyhydroxides species predominate at the surface of chalcopyrite. Therefore, applying the mediator concept, the initial alkaline flotation of sulphide ores turns into an oxide flotation case.