Efficient photoelectrochemical real textile wastewater detoxification using photoanodes of C3N4-BiVO4.

Photoelectrochemical systems utilizing solar energy have garnered significant attention for their sustainability in remediating contaminated water. This study focuses on advancing photoanode development through the utilization of carbon nitrides (C3N4) and bismuth vanadate (BiVO4), two promising semiconductor materials renowned for their efficient electron-hole pair separation leading to enhanced photocatalytic activity. Four distinct materials were synthesized and compared: BiVO4 over C3N4, C3N4 over BiVO4, and pristine BiVO4 and C3N4. Upon electrochemical analysis, the C3N4-BiVO4 heterostructure exhibited the highest photoelectrocatalytic charge transfer constant, mobility, and lifetime of charge carriers. Capitalizing on these exceptional properties, the composite was applied to remove organic matter real effluent from the textile industry. The photoelectrodegradation of the effluent demonstrated substantial removal of Total Organic Carbon (TOC) and the generation of low toxicity degradation products, accompanied by low energy consumption. The compelling results underscore the high potential of the synthesized C3N4-BiVO4 heterostructure for industrial applications, particularly in addressing environmental challenges associated with textile industry effluents.

Toward efficient electrocatalytic degradation of iohexol using active anodes: A laser-made versus commercial anodes.

The X-ray iodinated contrast medium iohexol is frequently detected in aquatic environments due to its high persistence and the inefficiency of its degradation by conventional wastewater treatments. Hence, the challenge faced in this study is the development of an alternative electrochemical treatment using active anodes. We investigate the oxidation of iohexol (16.42 mg L-1) using different operating conditions, focusing on the role of different mixed metal oxide anodes in the treatment efficiency. The electrocatalytic efficiency of the Ti/RuO2-TiO2 anode prepared using a CO2 laser heating and an ionic liquid is compared with Ti/RuO2-TiO2-IrO2 and Ti/IrO2-Ta2O5 commercial anodes. The hypochlorite ions generated by the anodes are also analyzed. The effect of the electrolyte composition (NaCl, Na2SO4, and NaClO4) and current density (15, 30, and 50 mA cm-2) on the iohexol degradation is also studied. The Ti/RuO2-TiO2 laser-made anode is more efficient than the commercial anodes. After optimizing experimental parameters, this anode removes 95.5% of iohexol in 60 min and displays the highest kinetic rate (0.059 min-1) with the lowest energy consumption per order (0.21 kWh m-3order-1), using NaCl solution as the electrolyte and applying 15 mA cm-2. Additionally, iohexol-intensified groundwater was used to compare the efficiency of anodes. The Ti/RuO2-TiO2 is also more efficient in removing the organic charge from the real water matrix (21.7% TOC) than the commercial anodes. Notably, the iohexol removal achieved is higher than all electrochemical treatments already reported using state-of-the-art non-active anodes in lower electrolysis time. Therefore, data from this study indicate that the electrochemical degradation of iohexol using the Ti/RuO2-TiO2 anode is efficient and has excellent cost-effectiveness; thus, it is a promising approach in the degradation of iohexol from wastewater. Furthermore, the Ti/RuO2-TiO2 active anode is competitive and can be an excellent option for treating effluents contaminated with recalcitrant organic compounds such as iohexol.

Novel Ti/RuO2IrO2 anode to reduce the dangerousness of antibiotic polluted urines by Fenton-based processes.

The treatment of hospital wastewater is very complex, so treating polluted human urine is a significant challenge. Here, we tested a novel MMO-Ti/RuO2IrO2 electrode to reduce the ecotoxicity risk of hospital urines contaminated with antibiotics. This electrode was used as the anode in electro-Fenton (EF) and photoelectro-Fenton (PhEF) processes. The results were compared with those obtained using the boron-doped diamond (BDD) anode, as well as those obtained by a conventional Fenton oxidation. In order to analyze the performance of the processes, the treatments were evaluated on the subject of Penicilin G (PenG) removal, toxicity (using a standardized method with Vibrio Fisheri), and antibiotic activity (Enterococcus faecalis as the target bacterium). The results reveal that PenG degrades in the following order: Fenton < EF < PhEF. The best results are found for the MMO-PhEF, which completely removed PenG, decreased 96% of toxicity, and completely removed antibiotic activity. Besides, for comparison, tests were performed with BDD, and results point out the higher convenience of the new electrode in terms of acceptable use of energy because the effluents generated can be further degraded in an urban wastewater treatment plant. Because of that, MMO-RuO2-IrO2 emerges as a promising cost-effective material for the pre-treatment of hospital urine effluents.

Influence of the doping level of boron-doped diamond anodes on the removal of penicillin G from urine matrixes.

The objective of this study is to understand the influence of the characteristics of boron-doped diamond anodes on the degradation of Penicillin G contained in urine. Therefore, five commercial BDD anodes with different boron doping levels (100 ppm - 8000 ppm) were studied. These electrodes were characterized by cyclic voltammetry, electrochemical impedance spectroscopy, and electrolysis. The boron doping was found to correlate well with the electrochemical properties of the electrodes, and results indicate a different behavior in drug degradation. The improvement in the toxicity and the reduction of the antibiotic effect of urine were the most innovative inputs monitored. For this, the concentration of Penicillin G, the toxicity toward Vibrio fisheri, and the antibiotic effect in Enterococcus faecalis were monitored. The best results were found for the BDD with a boron content of 200 ppm, capable of removing 100% of the antibiotic, reducing toxicity by 90%, and eradicating the antibiotic effect. These results indicate that low doping levels are more efficient for urine removal by anodic oxidation.