The objective of this work was to study the effect of muscovite and biotite on the flotation of chalcopyrite and molybdenite in seawater, and the use of sodium hexametaphosphate and sodium silicate to improve copper and molybdenum recoveries. The impact of the inorganic dispersants on the settling properties of the resulting flotation tailings was also studied. It was found that muscovite and biotite depress the flotation of chalcopyrite and molybdenite in seawater, with this depressing effect being stronger at pH 11 than at pH 9. Sodium hexametaphosphate and sodium silicate increased the recoveries of copper and molybdenum in seawater. These dispersants render the mineral particles more negatively charged and remove the hydroxy-complexes of magnesium and calcium from the mineral particles causing dispersion of the slimes. The settling rates of the flotation tailings slightly decrease when sodium hexametaphosphate and sodium silicate were added in the flotation stage. The presence of ultrafine particles dispersed by the action of the inorganic dispersants negatively impacted the flocculation and sedimentation processes leading to high flocculant consumption, low settling rates and high turbidity of the supernatant.

The mining industry is facing emerging challenges as a result of the increase in energy consumption and environmental demands. These facts have promoted the use of renewable energy sources, such as wind, geothermal and, mainly, solar energy. This paper discusses the role of solar energy (UV-VIS-NIR) in leaching processes, evaluating its potential application in metal extraction from sulfide minerals, based on photochemical mechanisms that promote the regeneration of ferric iron or the so called ferrous iron cycling. The present paper discusses the possibility that ultraviolet, visible light and near infrared irradiation (e.g., sunlight provided) can assist the leaching processes in two main ways: by the oxidation of sulfide minerals through in-situ generated Fenton-like reactions, and by the photochemical activation of semiconductor minerals that contain transition metals (Fe, Cu, and Cr, among others). Thus, this paper provides theoretical support to move towards the future application of photoleaching, which consist of a leaching process assisted by UV, VIS, and NIR irradiation. This technology can be considered a promising mineral processing route, using direct photochemical solar energy that can reduce the energy consumption (electricity, fuels) and the environmental impact, opening an opportunity for an alternative method of metal extraction from sulfide ores.

This paper review presents a comparison between conventional leaching and advanced photochemical leaching processes and their potential for use in chalcopyrite leaching. Likewise, it presents an analysis of the differences between the advanced leaching processes, photoleaching and radical-leaching, indicating that the photochemical mechanisms (photooxidation/photoreduction and generation of radical oxygen species (ROS) and radical sulfur species (RSS)) would improve the oxidative dissolution of chalcopyrite, taking advantage of the high oxidizing power of free radicals. Initial experimental results of solar-assisted radical-leaching on chalcopyrite are presented, demonstrating that sulfate radicals (SO₄⁻) allow copper to be leached at a rate 4.7 times higher than in the absence of radicals and sunlight. With these results, a radical-leaching process is presented for the first time, with a perspective toward the future development of a new hydrometallurgical route: solar-assisted radical-leaching.

Enargite (Cu₃AsS₄), a copper–arsenic sulfosalt, represents a critical challenge in copper mineral processing due to its high arsenic content, which poses significant environmental, metallurgical, and economic issues. Its flotation behavior closely resembles that of other copper sulfides such as chalcopyrite and chalcocite, complicating selective separation at early beneficiation stages. This review presents a comprehensive examination of enargite’s surface chemistry and electrochemical behavior, focusing on the influence of oxidation, pH, and pulp potential on surface reactivity, charge distribution (zeta potential), and hydrophobicity. Detailed insights into the formation of surface oxidation layers, passivation mechanisms, and contact angle variations are provided to elucidate collector-mineral interactions. Advances in selective flotation techniques are also discussed, including the use of depressant reagents, controlled redox environments, and reagent conditioning strategies. Special attention is given to flotation in seawater, where ionic strength and multivalent ions significantly influence mineral-reagent interactions and flotation outcomes. Galvanic interactions between enargite and other sulfide minerals are identified as critical factors affecting floatability and selectivity. The review consolidates findings from recent experimental and electrochemical studies, highlighting promising approaches to enhance enargite rejection and copper concentrate purity. It concludes with perspectives on future research aimed at optimizing flotation processes and developing sustainable solutions for processing arsenic-bearing copper ores.

This research investigates the fundamental impact of the photochemical effect of sunlight on the oxidative dissolution of chalcopyrite (CuFeS₂) in sulfate-oxidizing media under mild conditions and circumneutral pH. Beyond its traditional role as a thermal or electrical energy source, this study explores solar light (UV-Vis-NIR) as a photochemical reagent capable of driving the in situ generation of reactive sulfur species to assist the conventional oxidative dissolution pathway. The interaction at the mineral–solution interface under UV-Vis radiation was investigated using a laboratory-scale solar-assisted PS/TiO₂/UV-Vis-NIR system, employing persulfate (S₂O₈²⁻) as a radical precursor and TiO₂ (Aeroxide^® TiO₂ P25) as a photocatalyst. The findings demonstrate that solar exposure increases the system’s electrochemical potential and induces pH changes, which are critical for overcoming the inherent refractoriness of CuFeS₂ at near-neutral pH. This study demonstrates that integrating UV-Vis-NIR radiation serves as a synergistic catalyst in oxidative hydrometallurgical processes, enhancing Cu extraction yields to 14%–19% within 5 h of exposure at the laboratory scale. The use of natural light could offer a synergistic pathway to augment the efficiency of cleaner leaching technologies. These findings suggest that solar radiation could serve as a promising assistant to address kinetic limitations during the oxidative dissolution of complex sulfide ores under ambient conditions.