Search Results (6)

The increasing demand for sustainable energy and clean water has prompted the exploration of alternative solutions to reduce reliance on fossil fuels. In this context, hydrogen production through water electrolysis powered by solar energy presents a promising pathway toward a zero-carbon footprint. This study investigates the potential of copper slag, an abundant industrial waste, as a low-cost electrocatalyst for the hydrogen evolution reaction (HER) in contact with saline water such as 0.5 M NaCl and seawater, comparing the electrochemical response when in contact with geothermal water from El Tatio (Atacama Desert). The physicochemical characterisation of copper slag was performed using XRD, Raman, and SEM-EDS to determine its surface properties. Electrochemical evaluations were conducted in 0.5 M NaCl and natural seawater using polarisation techniques to assess the corrosion behaviour and catalytic efficiency of the copper slag electrodes. The results indicate that copper slag exhibits high stability and promising HER kinetics, particularly in seawater, where its mesoporous structure facilitates efficient charge transfer processes. The key novelty of this manuscript lies in the direct revalorisation of untreated copper slag as a functional electrode for HER in real seawater and geothermal water, avoiding the use of expensive noble metals and aligning with circular economy principles. This innovative combination of recycled material and natural saline electrolyte enhances both the technical and economic viability of electrolysis, while reducing environmental impact and promoting green hydrogen production in coastal regions with high solar potential. This research contributes to the value of industrial waste, offering a viable pathway for advancing sustainable hydrogen technologies in real-world environments. Full article

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. Full article

The mercury cell manufacturing process, which has been extensively used in chlor-alkali plants to produce chlorine and caustic soda by electrolysis, represents a major source of Hg environmental pollution. At Saline di Volterra (Tuscany, Italy), solution mining by pumping water into halite deposits was applied to produce brines for a mercury-cell chlor-alkali plant. The Hg-contaminated, exhausted brines were pumped back at depth into the rock salt field in order to renew the available resources. Activities ceased in 1994, following the leakage dispersion of highly contaminated Hg(0)-bearing brines into the environment. The mercury content in the soil, measured during a survey conducted in 2000, reached 334 mg/kg, highlighting diffuse contamination in the floodplain. By 2009, the Hg concentration had generally decreased and was mostly confined to the topsoil layer. In order to evaluate the present Hg soil pollution, a geochemical survey was carried out in 2023, almost thirty years after the contamination event. The obtained data indicated the occurrence of legacy Hg, which reached 25.5 mg/kg in some soil samples. Speciation analysis for the most contaminated soil revealed that Hg(0) represented about 17.3% of the total Hg and that water-soluble and organic Hg fractions were negligible. These results suggest that the originally released metallic mercury has volatilized and likely oxidized, becoming practically immobile in the soil. A risk assessment, performed by applying Hg speciation analysis, indicated that the mercury in the soil does not carry a risk of non-cancerous effects for different exposure routes in case of subsequent use of the site and that the formerly contaminated area can now be converted into a leisure area. Full article

Concentration followed by electrolysis is one of the most promising ways for saline wastewater treatment, since it could produce H₂, Cl_2, and an alkaline solution with deacidification potential. However, due to the diversity and difference of wastewater, knowledge on the suitable salt concentration for wastewater electrolysis and the effects of mixed ions are still lacking. In this work, electrolysis experiments of mixed saline water were conducted. The salt concentration for stable dechlorination was explored, with in-depth discussions on the effects of typical ions such as K⁺, Ca²⁺, Mg²⁺, and SO₄²⁻. Results showed that K⁺ had a positive effect on the H₂/Cl₂ production of saline wastewater through accelerating the mass transfer efficiency in the electrolyte. However, the existence of Ca²⁺ and Mg²⁺ had negative effects on the electrolysis performance by forming precipitates, which would adhere to the membrane, reduce the membrane permeability, occupy the active sites on the cathode surface, and also increase the transport resistance of the electrons in the electrolyte. Compared to Mg²⁺, the damaging effect of Ca²⁺ on the membrane was even worse. Additionally, the existence of SO₄²⁻ reduced the current density of the salt solution by affecting the anodic reaction while having less of an effect on the membrane. Overall, Ca²⁺ ≤ 0.01 mol/L, Mg²⁺ ≤ 0.1 mol/L and SO₄²⁻ ≤ 0.01 mol/L were allowable to ensure the continuous and stable dechlorination electrolysis of saline wastewater. Full article

The reverse electrodialysis heat engine (REDHE) is a promising salinity gradient energy technology, capable of producing hydrogen with an input of waste heat at temperatures below 100 °C. A salinity gradient drives water electrolysis in the reverse electrodialysis (RED) cell, and spent solutions are regenerated using waste heat in a precipitation or evaporation unit. This work presents a non-equilibrium thermodynamics model for the RED cell, and the hydrogen production is investigated for KCl/water solutions. The results show that the evaporation concept requires 40 times less waste heat and produces three times more hydrogen than the precipitation concept. With commercial evaporation technology, a system efficiency of 2% is obtained, with a hydrogen production rate of 0.38 g${}_{{\mathrm{H}}_2}$ m${}^{-2}$h${}^{-1}$ and a waste heat requirement of 1.7 kWh g${}_{{\mathrm{H}}_2}^{-1}$. The water transference coefficient and the salt diffusion coefficient are identified as membrane properties with a large negative impact on hydrogen production and system efficiency. Each unit of the water transference coefficient in the range $t_w=\left[0–10\right]$ causes a −7 mV decrease in unit cell electric potential, and a −0.3% decrease in system efficiency. Increasing the membrane salt diffusion coefficient from 10${}^{-12}$ to 10${}^{-11}$ leads to the system efficiency decreasing from 2% to 0.6%. Full article

Saline water electrolysis (SWE) is an electrochemical process to simultaneously produce hydrogen (H₂), chlorine (Cl₂), and sodium hydroxide (NaOH) with high purity levels (e.g., 99.999%) by applying electric power to saline water. The state-of-the art SWE membrane, Flemion^®, has excellent chemical resistance to harsh SWE conditions, but still needs to lower its energy consumption by reducing its ohmic resistance to Na⁺ ion transport. Meanwhile, most of cation exchange membranes (CEMs) have been suffering from chemical degradation under the alkaline conditions, owing to their single layer matrices composed of sulfonic acid moieties, though they show fast Na⁺ ion transport behavior. Here double-layered SWE membranes were prepared on the basis of design strategies composed of the incorporation of a chemically stable carboxylic acid layer (C layer) via UV irradiation onto one surface of perfluorinated Nafion^®212 membrane chosen as one of commercially available CEMs, and the thickness control of the C layer. The resulting membranes showed excellent SWE performances and improved electrochemical service life, when compared with those of Nafion^®212 and Flemion^®, respectively. Full article