This study investigates the effect of temperature on the rate of the oxygen evolution reaction (OER) during the electrochemical production of ferrate(VI) through anodic iron dissolution. We employed a membrane-divided electrochemical cell with a galvanostatically operated three-electrode setup. During the experiments, we recorded the anode potential at various temperatures and monitored temperature variations over time. Simultaneously, we measured the rates of ferrate(VI) formation and the oxygen evolution reaction. The latter, considered a parasitic reaction, competes with ferrate synthesis. By quantifying the extent to which the OER consumed the applied charge, we discovered that the OER rate decreases with temperature. Specifically, at 25 °C and 168 Am⁻², the OER consumes more than double the charge of the produced ferrate, at higher temperatures the rate sensibly decays and with it the consumed charge by the OER. The specific energy required for ferrate(VI) production decreases as temperatures increase, aligning well with current efficiency and space-time yield values within the same temperature range.

This study proposes a fuzzy control strategy embedded in a Siemens IoT2040 gateway developed for removing inorganic arsenic from synthetic underground water in a treatment plant prototype. The prototype is used to dose a constant flow of Fe(VI) to maintain an oxide-reduction potential to guarantee the oxidation of arsenite into arsenate, while the fuzzy logic embedded in the IoT control manages the addition of Fe(III) to achieve a proper pH adjustment and efficient arsenate removal. The tests used synthetic Bangladesh groundwater enriched with 200 µg/L of arsenite and 200 µg/L of arsenate. The results revealed that the plant prototype yielded an effective treatment of the water. Arsenate was decreased to an average value of 6.66 µg/L and, the arsenite concentration decreased to 1.01 µg/L or less. These values were lower than the limit of 10 µg/L deemed by the World Health Organization as safe for human consumption.

Arsenic is an inorganic pollutant that, depending on oxidation–reduction and pH level conditions, may be found in natural waters in two variants: As(III) and As(V). Any treatment to effectively remove arsenic from water will be conditioned by the presence of one or both variants. In this context, this study assesses using electrochemically produced Fe(VI) with Fe(III) to remove As(III), As(V), and their combinations from the Synthetic Bangladesh Groundwater (SBGW) containing anions that interfere with iron-based arsenic removal processes. The combined use of Fe(VI) and Fe(III) allowed us to remove the total arsenic below the 10 mg L⁻¹ threshold established by the World Health Organization and Peruvian regulations for drinking water. An optimum combination of 1 mg L⁻¹ of Fe(VI) and 30 mg L⁻¹ of Fe(III) was identified and tested on the removal of four different proportions of As(III):As(V) for two total concentrations: 500 and 250 mg L⁻¹. There were no significant differences in the final removal values under the different proportions of As(III):As(V) for each total concentration, with a final removal average of 99.0% and 96.9% for the 500 and 250 µg L⁻¹ concentrations, respectively.

This study presents the results of ultraviolet radiation measurement in a truncated compound parabolic concentrator. The measurements were performed by usi