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Ag-based electrical contact materials are essential in low-voltage devices such as relays, switches, circuit breakers, and contactors. Historically, Ag-CdO composites have been preferred due to their superior electrical and thermal conductivities, resistance to arcing, and mechanical strength. However, the toxicity of Cd has led to increased restrictions on its use. With the aim of contributing to the development of a new environment-friendly, Ag-Zn2SnO4-based electrical contact material, the kinetics of the hot mechanochemical oxidation of a Ag-Sn-Zn solid solution obtained by mechanical alloying were investigated. The results indicated that the proposed synthesis route produces Ag-based composites with a homogeneous distribution of nanoscale Zn2SnO4 precipitates, which is unattainable through conventional material processing methods. This kinetic study established that the mechanochemical oxidation of the Ag-Sn-Zn solid solution follows the Johnson–Mehl–Avrami–Kolmogorov model. An analysis of the microstructure and the relationship between the activation energy “Ea” and the Avrami exponent “n” from experimental data fitting suggests that the primary mechanism for the oxidation of the Ag-Sn-Zn solid solution during the hot mechanochemical process is related to the three-dimensional oxide growth being limited by oxygen diffusion after its immediate initial nucleation.

Solar saline water splitting is a promising approach to sustainable hydrogen production, harnessing abundant solar energy and the availability of brine resources, especially in the Atacama Desert. Bischofite salt (MgCl2·6H2O) has garnered significant attention due to its wide range of industrial applications. Efficient hydrogen production in arid or hyper arid locations using bischofite solutions is a novel and revolutionary idea. This work studied the electrochemical performance of Mn2O3 electrodes using a superposition model based on mixed potential theory and evaluated the superficial performance of this electrode in contact with a 0.5 M bischofite salt solution focusing on the hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR) that occur during saline water splitting. The application of the non-linear superposition model provides valuable electrochemical kinetic parameters that complement the understanding of Mn2O3, this being one of the novelties of this work.

The presence of clays in copper minerals has a significant negative impact during their processing, leading to low recoveries during the flotation process. In saline environments, the presence of these clays promotes operational problems associated with salinity, leading to decreases in the copper concentrate grade, alterations in the rheology of the mineral pulp, reduction in the selectivity of copper during the flotation process, declines in the quality of clarified water, and excessive corrosion of metallic components. This study explores the electroflotation of kaolinite and montmorillonite clays in NaCl solutions using a modified Hallimond tube coupled with Ti Gr. 2 electrodes for bubble generation via water electrolysis and the corrosion analysis of these electrodes applying the superposition model. The electroflotation results show recovery of clays close to 72.68% for kaolinite, 88.44% for montmorillonite, and 67.36% for a mixture of both clays. The presence of clays helps reduce the corrosive effects of Ti Gr. 2 from 0.069 A/m2 in NaCl to 0.0073 A/m2 in NaCl with montmorillonite clay.

In Northern Chile, large amounts of highly corrosive solutions are currently generated in the process of cathode washing after completing the electrowinning or electrorefining process of copper. This study investigates the electrochemical behavior of ASTM A36 carbon steel in pregnant-leach-solution (PLS) wash water. Measurements of electrochemical impedance spectroscopy and linear sweep voltammetry, complemented with weight loss measurements, were performed. Four ratios of PLS containing reverse osmosis (RO) water are evaluated, considering both quiescent and rotating conditions of the steel specimen. The results indicate that oxygen reduction, hydrogen evolution, and iron oxidation reactions are all involved during the corrosion of carbon steel in pure RO water, with the corrosion rate increasing up to 4 times under rotating conditions. In the case of corrosion in RO wash water containing PLS, a galvanic process occurs whereby copper is reduced at the expense of iron oxidation, superimposed on former partial reactions. The deposited copper induces notable corrosion inhibition of steel, observed as a significant drop in corrosion rate from high initial to constant residual values. Morphological and X-ray analyses support that corrosion is affected by oxide layer formation and galvanic copper deposition, confirming the results obtained from electrochemical analysis and weight loss measurements.

The electrochemical ion pumping device is a promising alternative for the development of the industry of recovering metals from natural sources—such as seawater, geothermal water, well brine, or reverse osmosis brine—using electrochemical systems, which is considered a non-evaporative process. This technology is potentially used for metals like Li, Cu, Ca, Mg, Na, K, Sr, and others that are mostly obtained from natural brine sources through a combination of pumping, solar evaporation, and solvent extraction steps. As the future demand for metals for the electronic industry increases, new forms of marine mining processing alternatives are being implemented. Unfortunately, both land and marine mining, such as off-shore and deep sea types, have great potential for severe environmental disruption. In this context, a green alternative is the mixing entropy battery, which is a promising technique whereby the ions are captured from a saline natural source and released into a recovery solution with low ionic force using intercalation materials such as Prussian Blue Analogue (PBA) to store cations inside its crystal structure. This new technique, called “electrochemical ion pumping”, has been proposed for water desalination, lithium concentration, and blue energy recovery using the difference in salt concentration. The raw material for this technology is a saline solution containing ions of interest, such as seawater, natural brines, or industrial waste. In particular, six main ions of interest—Na+, K+, Mg2+, Ca2+, Cl−, and SO42−—are found in seawater, and they constitute 99.5% of the world’s total dissolved salts. This manuscript provides relevant information about this new non-evaporative process for recovering metals from aqueous salty solutions using hexacianometals such as CuHCF, NiHCF, and CoHCF as electrodes, among others, for selective ion removal.

The deterioration of reinforced concrete structures in marine environments presents multiple problems due to the premature degradation of reinforced steel. This work aimed to study the corrosion of reinforced A630-420H steel when exposed to a 0.5 M NaCl solution. Although this carbon steel is the most widely used material for reinforced concrete structures in Chile, there is limited research on its resistance to corrosion when in contact with saline solutions. The electrochemical reactions and their roles in the corrosion rate were studied using linear sweep voltammetry, weight loss, scanning electron microscopy, and X-ray diffraction techniques. This analysis is unique as it used the superposition model based on mixed potential theory to determine the electrochemical and corrosion parameters. The outcomes of this study show that A630-420H steel has a higher corrosion rate than those of the other commercial carbon steels studied. This fact can be attributed to the competition between the cathodic oxygen reduction reaction and hydrogen evolution reaction, which also depends on the environmental conditions, exposure time, stabilization of the corrosion products layer, and presence of chloride ions. Additionally, the results under mechanical stress conditions show a brittle fracture of the corrosion product oriented longitudinally in the direction of the bend section, where the presence of pores and cracks were also observed. The corrosion products after corrosion were mainly composed of magnetite and lepidocrocite oxide phases, which is in concordance with the electrochemical results.

Cellular automata models have emerged as a valuable tool in corrosion management. This manuscript provides an overview of the application of cellular automata models in corrosion research, highlighting their benefits and contributions to understanding the complex nature of corrosion processes. Cellular automata models offer a computational approach to simulating corrosion behavior at the microscale, capturing the intricate interactions between electrochemical reactions, material properties, and environmental factors and generating a new vision of predictive maintenance. It reviews the key features of cellular automata, such as the grid-based representation of the material surface, the definition of state variables, and the rules governing cell-state transitions. The ability to model local interactions and emergent global behavior makes cellular automata particularly suitable for simulating corrosion processes. Finally, cellular automata models offer a powerful and versatile approach to studying corrosion processes, expanding models that can continue to enhance our understanding of corrosion and contribute to the development of effective corrosion prevention and control strategies.

The leaching of minerals is one of the main unit operations in the metal dissolution process, and in turn it is a process that generates fewer environmental liabilities compared to pyrometallurgical processes. As an alternative to conventional leaching methods, the use of microorganisms in mineral treatment processes has become widespread in recent decades, due to advantages such as the non-production of emissions or pollution, energy savings, low process costs, products compatible with the environment, and increases in the benefit of low-grade mining deposits. The purpose of this work is to introduce the theoretical foundations associated with modeling the process of bioleaching, mainly the modeling of mineral recovery rates. The different models are collected from models based on conventional leaching dynamics modeling, based on the shrinking core model, where the oxidation process is controlled by diffusion, chemically, or by film diffusion until bioleaching models based on statistical analysis are presented, such as the surface response methodology or the application of machine learning algorithms. Although bioleaching modeling (independent of modeling techniques) of industrial (or large-scale mined) minerals is a fairly developed area, bioleaching modeling applied to rare earth elements is a field with great growth potential in the coming years, as in general bioleaching has the potential to be a more sustainable and environmentally friendly mining method than traditional mining methods.

The solar electroflotation (EF) processes using saline electrolytes are today one of the great challenges for the development of electrochemical devices, due to the corrosion problems that are generated during the operation by being in permanent contact with Cl− ions. This manuscript discloses the corrosion behavior of titanium electrodes using a superposition model based on mixed potential theory and the evaluation of the superficial performance of the Ti electrodes operated to 4 V/SHE solar electroflotation in contact with a solution of 0.5 M NaCl. Additionally provided is an electrochemical analysis of Ti electrodes regarding HER, ORR, OER, and CER that occur during the solar saline EF process. The non-linear superposition model by mixed potential theory gives electrochemical and corrosion parameters that complement the information published in scientific journals, the corrosion current density and corrosion potential in these conditions is 0.069 A/m2 and −7.27 mV, respectively. The formation of TiO2 and TiOCl on the anode electrode was visualized, resulting in a reduction of its weight loss of the anode electrode.

The presence of ultrafine clay particles that are difficult to remove by conventional filtration creates many operational problems in mining processing systems. In this work, the removal of clay suspensions has been investigated using an electroflotation (EF) process with titanium electrodes. The results show that EF is a viable and novel alternative for removing ultrafine particles of kaolinite-type clay present in sedimentation tank overflows with low salt concentrations (

Analytical models are of vital importance to study the dynamics of complex systems, including the heap leaching process. In this work, a methodology to study the dynamics of copper recovery in the heap leaching by means of fit of analytical models that capture the leaching dynamics product of variations of leaching agents as a function of the feeding is proposed, establishing a first mode of operation keeping the leaching agent fixed (H2SO4) and a second operation mode, where Cl− is added to accelerate the reaction kinetics of sulfide minerals (secondary sulfides). Mineral recovery was modeled for the different modes of operation, dependent on the independent variables/control parameters time, heap height, leach flow rate, and feed granulometry. The results indicate that the recovery of ore from sulfide minerals is proportional to the addition of Cl−, reaching recovery levels of approximately 60%, very close to 65% recovery in conventional oxide leaching, using only H2SO4 as leaching agent. Additionally, high copper recoveries from sulfide ores are achieved at medium Cl− concentrations, but the increase in recovery at high Cl− concentrations is marginal.

This work reports on the electrochemical kinetic analysis of carbon steel powders produced during the milling of carbon steel chips for 2, 3, and 5 h under an air atmosphere in a high-energy ball miller. This work aims to fill the gap in the literature regarding the transformation processes that affect carbon steel powder production. This information can be crucial for specific powder metallurgy systems. The results obtained using the Rietveld refinement method showed a decrease in the crystallite size, an increase in the microstrain, and no changes in the lattice parameter with the milling process. The electrochemical results revealed a strong influence of anodic electroactivity with milling time in NaCl solution, in contrast with NaOH, where the influence of the milling process was not significant. These results clearly show the significant role of chloride ions in preventing the formation of a passive film in milling with NaCl solution and in contrast to the formation of a passive film that notoriously inhibits both the anodic and cathodic reactions in milling with NaOH solution. The novelty of this work lies in the experimental demonstration of milling’s influence on the surface properties of carbon steel powders that directly affect their electrochemical response.

The presence of micro and nanoplastics in the food chain constitutes an emergent multifactorial food safety and physiological stress problem, which must be approached with a strategic perspective since it affects public health when consuming products that have this pollutant, such as fish and crustaceans, fruits, and vegetables. In this review, the authors present the results by scientists from different disciplines who are dedicated to discovering their chemical constitution and origin, the contents of these microparticles in edible plants, the contamination of water-irrigated soils, the mechanisms that concentrate microplastics in these soils, methods to determine them, contamination of freshwater sources of cities, and the negative effect of nano and microplastics on various food products and their detrimental impact on the environment. Recent findings of plant uptake mechanisms complement this, but more research is needed.

The average lithium content in the Earth’s crust is estimated at about 0.007%. Despite this, lithium is considered abundant and widely distributed, with significant extraction from various sources. Notably, the brines in the Salar de Atacama are highlighted for their high lithium concentration ~1800 mg/L. Lithium is currently recovered from these brines through a solar evaporation process. The brine is transferred through a series of ponds, increasing the lithium concentration from 0.2% to 6% over 18 months, while decanting other minerals like potassium, magnesium, and boron. This method is the most efficient and cost-effective globally due to the Salar de Atacama’s high lithium concentration of approximately 1800 ppm and the region’s intense solar radiation, which facilitates evaporation at no economic cost. This manuscript describes in detail the lithium and potassium extraction processes used in the Salar de Atacama.

Photovoltaic technology has proven to be a reliable, economical, and clean energy source that is capable of adapting to diverse geographical conditions. However, factors such as soiling overshadow these qualities, thus leading to production losses and affecting the profitability of this technology. For these reasons, soiling is a highly studied topic, which involves considering the physicochemical characterization of the deposited material, mitigation strategies, effect predictions, and cleaning mechanisms. However, there is a relatively unexplored area related to the microbiological contribution to soiling. The surface of photovoltaic modules, along with the deposited material and local atmospheric factors, fosters favorable conditions for the colonization of microorganisms. These microorganisms influence the soiling mechanisms and optical properties of photovoltaic modules. This work presents a detailed characterization of the microbial diversity present in the soiling deposited on photovoltaic modules installed in the Atacama Desert. Two study sites were defined: Antofagasta and the Solar Platform of the Atacama Desert, which have warm and cold desert climates, respectively. Mineralogical characterization tests, heavy metal analyses, TOC, and inorganic element analyses were conducted on the deposited material. Additionally, the culturable isolates and the metagenomic DNA of the soiling samples and biofilms grown on standard PV glass were characterized using next-generation sequencing. The results show that the deposited soiling contained a microbiological component that had adapted to extreme desert conditions. The presence of the genera Arthrobacter, Kocuria, and Dietzia were identified in the culturable isolates from Antofagasta, while Arthrobacter and Dietzia were obtained from the Solar Platform of the Atacama Desert. The metagenomic DNA was mainly represented by the genera Pontibacter, Noviherbaspirillum, Massilia, Arthrobacter, Hymenobacter, and Deinococcus at Antofagasta. However, at the Solar Platform of the Atacama Desert, the analyzed samples presented DNA concentrations below 0.5 ng/µL, which made their preparation unviable. At the PSDA, the biofilms formed by the genera Peribacillus and Kocuria were identified, whereas the UA showed a greater abundance of bacteria that favored biofilm formation, including those that belonged to the genera Bacillus, Sporosarcina, Bhargavaea, Mesaobacillus, Cytobacillus, Caldakalibacillus, and Planococcus. Based on these results, we propose a soiling mechanism that considers the microbiological contribution to material cementation.

Ferromanganese crusts are mineral resources distributed in the planet’s oceans. These deep-sea minerals stand out for their abundance and diversity of metals, with Mn and Co being the most abundant elements. These minerals are a good alternative to diversify the extraction of elements, which today are found at low grades on the Earth’s surface. For the co-processing of ferromanganese crusts to recover Co and Mn, there are few studies. These generally worked with the use of a reducing agent, and in many cases previous roasting processes. In the present investigation, two ferromanganese crusts that were collected from two seamounts in the central eastern Atlantic Ocean were characterized. Subsequently, these crusts were leached in an acid-reducing medium, adding steel waste (slag) with 99.73% Fe3O4 and 0.27% metallic iron from the steel industry as a reducing agent. Acid-reducing processes have previously been shown to yield high and rapid recoveries of Co and Mn from seabed minerals. However, there is no previous study using smelting slag as a reducing agent for the treatment of ferromanganese crusts. The best results of this research were obtained when working at 60 C, achieving joint extractions of Co and Mn of ~80% and ~40%, respectively, in 10 min. In addition, the process residues were analyzed, and the formation of contaminating elements or the precipitation of Co and Mn species was not observed.

Green hydrogen is poised to play a crucial role in the energy-transition process in developed countries over the coming years, particularly in those countries aiming to achieve net-zero emissions. Consequently, the for green hydrogen is expected to rise significantly. This article explores the fundamental methods of producing hydrogen, focusing on the oxidation reaction within a thermochemical solar cycle for the dissociation of steam. Solar thermochemical cycles have been extensively researched, yet they remain in the development stage as research groups strive to identify optimal materials and conditions to enhance process efficiency, especially at high temperatures. The article analyses theoretical foundations drawn from exhaustive scientific studies related to the oxidation of iron in steam, the relationship with the activation energy of the corrosive process, thermodynamic aspects, and the kinetic model of a heterogeneous reaction. Additionally, it presents various mechanisms of high-temperature oxidation, pH effects, reactors, and materials (including fluidized beds). This scientific review suggests that hydrogen production via a thermochemical cycle is more efficient than production via electrochemical processes (such as electrolysis), provided the limitations of the cycle’s reduction stage can be overcome.

Corrosion is an inevitable and persistent issue that affects various metallic infrastructures, leading to significant economic losses and safety concerns, particularly in areas near or in contact with saline solutions such as seawater. Green corrosion inhibitors are compounds derived from natural sources that are biodegradable in various environments, offering a promising alternative to their conventional counterparts. Despite their potential, green corrosion inhibitors still face several limitations and challenges when exposed to NaCl environments. This comprehensive review delves into these limitations and associated challenges, shedding light on the progress made in addressing these issues and potential future developments as tools in corrosion management. Explicitly the following aspects are covered: (1) attributes of corrosion inhibitors, (2) general corrosion mechanism, (3) mechanism of corrosion inhibition in NaCl, (4) typical electrochemical and surface characterization techniques, (5) theoretical simulations by Density Functional Theory, and (6) corrosion testing standards and general guidelines for corrosion inhibitor selection. This review is expected to advance the knowledge of green corrosion inhibitors and promote further research and applications.

Solar thermal plants typically undergo trough operational cycles spanning between 20 and 25 years, highlighting the critical need for accurate assessments of long-term component evolution. Among these components, the heat storage media (molten salt) is crucial in plant design, as it significantly influences both the thermophysical properties of the working fluid and the corrosion of the steel components in thermal storage systems. Our research focused on evaluating the long-term effects of operating a low-melting-point ternary mixture consisting of 30 wt% LiNO3, 57 wt% KNO3, and 13 wt% NaNO3. The ternary mixture exhibited a melting point of 129 °C and thermal stability above 550 °C. Over 15,000 h, the heat capacity decreased from 1.794 to 1.409 J/g °C. Additionally, saline components such as CaCO3 and MgCO3, as well as lithium oxides (LiO and LiO2), were detected due to the separation of the ternary mixture. A 30,000 h exposure resulted in the formation of Fe2O3 and the presence of Cl, indicating prolonged interaction with the marine environment. This investigation highlights the necessity of analyzing properties under actual operating conditions to accurately predict the lifespan and select the appropriate materials for molten salt-based thermal storage systems.

Excess energy derived from photosynthesis can be used in plant microbial fuel cell (PMFC) systems as a sustainable alternative for the generation of electricity. In this study, the in situ performance of CAM (Crassulacean acid metabolism) plants in Calama, in the Atacama Desert, was evaluated for energy recovery using PMFCs with stainless steel AISI 316L and Cu as electrodes. The plant species evaluated included Aloe perfoliata, Cereus jamacaru, Austrocylindropuntia subulata, Agave potatorum, Aloe arborescens, Malephora crocea, and Kalanchoe daigremontiana. Among the plant species, Kalanchoe daigremontiana demonstrated significant potential as an in situ PMFC, showing a maximum cell potential of 0.248 V and a minimum of 0.139 V. In addition, the cumulative energy for recovery was about 9.4 mWh m−2 of the electrode. The use of CAM plants in PMFCs presents a novel approach for green energy generation, as these plants possess an inherent ability to adapt to arid environments and water-scarce areas such as the Atacama Desert climate.