Hybrid adsorbent, based on the cross-linked copolymer impregnated with hydrous iron oxide, was applied for the first time for Se(VI) adsorption from water. The influence of the initial solution pH, selenate concentration and contact time to adsorption capacity was investigated. Adsorbent regeneration was explored using a full factorial experimental design in order to optimize the volume, initial pH value and concentration of the applied NaCl solution as a reagent. Equilibrium state was described using the Langmuir model, while kinetics fitted the pseudo-first order. The maximum adsorption capacity was found to be 28.8 mg/g. Desorption efficiency increased up to 70%, and became statistically significant with the reagent concentration and pH increase, while the applied solution volume was found to be insignificant in the investigated range. Based on the results obtained, pH influence to the adsorption capacity, desorption efficiency, Fourier transform infrared (FTIR) and X-ray diffraction (XRD) analysis of loaded adsorbent, it was concluded that the outer- and inner-sphere complexation are mechanisms responsible for Se(VI) separation from water. In addition to the experiments with synthetic solutions, the adsorbent performances in drinking water samples were explored, showing the purification efficiency up to 25%, depending on the initial Se(VI) concentration and water pH. Determined sorption capacity of the cross-linked copolymer impregnated with hydrous iron oxide and its ability for regeneration, candidate this material for further research, as a promising anionic species sorbent.

The electrorefining process of the non-commercial Cu anodes was tested on the enlarged laboratory equipment over 72 h. Cu anodes with Ni content of 5 or 10 wt.% and total content of Pb, Sn, and Sb of about 1.5 wt.% were used for the tests. The real waste solution of sulfuric acid character was a working electrolyte of different temperatures (T1 = 63 ± 2 °C and T2 = 73 ± 2 °C). The current density of 250 A/m² was the same as in the commercial process. Tests were confirmed that those anodes can be used in the commercial copper electrorefining process based on the fact that the elements from anodes were dissolved, the total anode passivation did not occur, and copper is deposited onto cathodes. The masses of cathode deposits confirmed that the Cu ions from the electrolyte were also deposited onto cathodes. The concentration of Cu, As, and Sb ions in the electrolyte was decreased. At the same time, the concentration of Ni ions was increased by a maximum of up to 129.27 wt.%. The major crystalline phases in the obtained anode slime, detected by the X-ray diffraction analyses, were PbSO₄, Cu₃As, SbAsO₄, Cu₂O, As₂O₃, PbO, SnO, and Sb₂O₃.

This paper considers the impact of copper mining-influenced water and metallurgical wastewater on the surface water in the Bor area, Serbia. Sampling, realized through the four campaigns (2020–2021), confirmed that both types of water, discharged without appropriate treatment in the Bor River, had a signific impact on the concentration of metal ions, pH and electrical conductivity on the watercourse in the Bor area. The highest concentrations of the following metal ions, Cu—271 mg/L, As—25,991 μg/L, Ni—13,856 μg/L, Cd—2627 μg/L, and Pb—2855 μg/L, were registered in the metallurgical wastewater samples. After changes occurred in the copper production process by stopping the discharge of untreated wastewater into the Bor River, the concentrations of monitored elements were drastically decreased. In the period 2022–2024, the concentration values for Cu, As and Pb ions were below the maximum allowable value, and the concentration values of Ni and Cd ions were also decreased. The values for pH and electrical conductivity were in the maximum allowable range. The return of wastewater to the copper production process would lead to both a reduction in the primary water consumption and reduction in the negative impact on the environment.

Highly porous lignin-based microspheres, modified by magnetite nanoparticles, were used for the first time for the removal of selenate anions, Se(VI), from spiked and real water samples. The influence of experimental conditions: selenate concentration, adsorbent dosage and contact time on the adsorption capacity was investigated in a batch experimental mode. The FTIR, XRD, SEM techniques were used to analyze the structural and morphological properties of the native and exhausted adsorbent. The maximum adsorption capacity was found to be 69.9 mg/g for Se(VI) anions at pH 6.46 from the simulated water samples. The modified natural polymer was efficient in Se(VI) removal from the real (potable) water samples, originated from six cities in the Republic of Serbia, with an overage efficacy of 20%. The regeneration capacity of 61% in one cycle of desorption (0.5 M NaOH as desorption solution) of bio-based adsorbent was gained in this investigation. The examined material demonstrated a significant affinity for Se(VI) oxyanion, but a low potential for multi-cycle material application; consequently, the loaded sorbent could be proposed to be used as a Se fertilizer.

Development of adsorption materials based on metal oxides, silicon dioxide, carbon, biosorbents and adsorbents, obtained from natural waste, can be used to remove selenium from water. Research on some of these materials is at the laboratory level, while the others were tested in the pilot plants, and a few have found a commercial application. The high adsorption capacities show a possibility of their application for selenium removal from water. This paper presents a literature review of different types of adsorbents for the removal of selenium (Se) from water.

This study focuses on Pb²⁺ and As(V) adsorption on mineral heterostructures based on a mixture of Si, Fe, and Ti oxides (MOHs). Various techniques were performed to analyze the morphological and structural properties of the synthesized metal oxide samples. In addition to the experimental optimization of the parameters determined by the response surface method (RSM), the effects of pH, adsorbent dosage, temperature, and contact duration on the batch and column system adsorption efficiency of single-component and simultaneous lead and arsenate removal were tested. The pseudo-second-order kinetic model and Weber–Morris model were more relevant to the adsorption on the metal(loid)s. The adsorption of Pb²⁺ was related to the Langmuir isotherm model, while the adsorption of As(V) was fitted to the Freundlich isotherm model. The thermodynamic parameters indicate the spontaneity of the adsorption process with a low endothermic character. The MOHs were more effective in removing Pb²⁺ and As(V) in the multi-component system (87.7 and 46.1%, respectively) than in the single-component system (56.3 and 23.4%, respectively). This study demonstrates that mineral heterostructures can be effectively used to remove cations and anions from water systems, and due to their fast kinetics, they can be applied to the needs of rapid interventions after pollution.