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In the current work, the hybrid process potential of ultrasound (US) and electro-Fenton (EF), named sono-electro-Fenton (SEF), was fully investigated for sulfadiazine (SDZ) degradation. The decontamination in the integration approach was revealed to be greater than in individual procedures, i.e., EF process (roughly 66%) and US process (roughly 15%). The key operating process factors (i.e., applied voltage, H2O2 content, pH, initial concentration of SDZ, and reaction time) affecting SDZ removal were evaluated and optimized using Box-Behnken Design (BBD). In addition, an adaptive neuro-fuzzy inference system (ANFIS) as an efficient predictive model was applied to forecast the decontamination efficiency of SDZ through the SEF process based on the same findings produced from BBD. The results revealed that the predictability of SDZ elimination by the ANFIS and BBD approaches exhibited an excellent agreement (a greater R2 of 0.99%) among the both models. Density functional theory was also employed to forecast the plausible decomposition elucidation by the bond-breaking mechanism of organic substances. Plus, the main side products of SDZ degradation during the SEF process were tracked. Eventually, the non-carcinogenic risk assessment of different samples of natural water containing SDZ that was treated by adopting US, EF, and SEF processes was examined for the first time. The findings indicated that the non-carcinogenic risk (HQ) values of all the purified water sources were computed in the permissible range. [ABSTRACT FROM AUTHOR]

The problem of the deep elimination of antibiotics in environmental bodies is exceptionally warranted. In this work, a ternary nanocomposite of FeNi3/SiO2/CuS (FSC) was fabricated and then integrated with UV light irradiation and hydrogen peroxide as the heterogeneous Fenton-like photocatalytic system for the decomposition of tetracycline (TC) from aqueous media. During this process, various influencing parameters such as pH, catalyst dosage, initial content of TC, hydrogen peroxide (H2O2) dose, and operating time were explored. At optimized circumstances, i.e., 5 of pH, 10 mg/L of TC concentration, 150 mg/L of H2O2 dosage, and 200 min of degradation time, the elimination proportion of TC was 96%. The results of capture agent tests clarified that hydroxyl radical (HO•) played the predominant role in the photocatalytic decontamination of TC. Moreover, with the elevated contact time and content of H2O2, the efficiency of TC decontamination increased significantly. Additionally, the findings of the stability and reusability experiments of the fabricated nanocomposite showed that the percentage of TC removal decreased by only about 5% after six cycles. Furthermore, the photocatalytic mechanism of the decontamination of TC over the FSC photocatalyst was elucidated. Eventually, the non-carcinogenic risk analysis in the surface water sample was carried out using multiple photocatalytic processes for the first time. These outcomes obtained in this study validate that coupling the photocatalytic system and the H2O2 oxidation agent facilitates the elimination of a great variety of pharmaceutical contaminants from aqueous media. [ABSTRACT FROM AUTHOR]