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The increasing use of pharmaceuticals and the ongoing release of drug residues into the environment have resulted in significant threats to environmental sustainability and water safety. In this sense, developing a robust and easy-recovered magnetic nanocomposite with eminent photocatalytic activity is very imperative for detoxifying pharmaceutical compounds. Herein, a systematic study was conducted to investigate the photocatalytic ozonation for eliminating metronidazole (MET) from aqueous media utilizing the CuFe2O4/SiO2/ZnO heterojunction under simulated sunlight irradiation. The composite material was fabricated by a facile hydrothermal method and diagnosed by multiple advanced analytical techniques. Modelling and optimization of MET decontamination by adopting the central composite design (CCD) revealed that 90 % of MET decontamination can be achieved within 120 min of operating time at the optimized circumstance (photocatalyst dose: 1.17 g/L, MET dose: 33.20 mg/L, ozone concentration: 3.99 mg/min and pH: 8.99). In an attempt to scrutinize the practical application of the CuFe2O4/SiO2/ZnO/xenon/O3 system, roughly 56.18% TOC and 73% COD were removed under the optimized operational circumstances during 120 min of degradation time. According to the radical quenching experiments, hydroxyl radicals (HO•) were the major oxidative species responsible for the elimination of MET. The MET degradation rate maintained at 83% after seven consecutive runs, manifesting the efficiency of CuFe2O4/SiO2/ZnO material in the MET removal. Ultimately, the photocatalytic ozonation mechanism over the CuFe2O4/SiO2/ZnO heterojunction of the fabricated nanocomposites was rationally proposed for MET elimination. In extension, the results drawn in this work indicate that integrating photocatalyst and ozonation processes by the CuFe2O4/SiO2/ZnO material can be applied as an efficient and promising method to eliminate tenacious and non-biodegradable contaminants from aqueous environments.

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The present work proposes an ultrasound (US) assisted electro-Fenton (EF) process for eliminating penicillin G (PNG) and ciprofloxacin (CIP) from aqueous solutions and the process was further optimized by response surface methodology (RSM)- Box-Behnken design (BBD). The impact of pH, hydrogen peroxide (H2O2) concentration, applied voltage, initial pollutant concentration, and operating time were studied. The capability application of the electro-Fenton (EF) and US processes was compared separately and in combination under the optimum conditions of pH of 4, a voltage of 15 V, the initial antibiotic concentration of 20.7 mg/L, H2O2 concentration of 0.8 mg/L, and the operating time of 75 min. The removal efficiency of PNG and CIP using the sono-electro-Fenton (SEF) process, as the results revealed, was approximately 96% and 98%, respectively. The experiments on two scavengers demonstrated that ⦁OH contributes significantly to the CIP and PNG degradation by SEF, whereas ⦁O-2 corresponds to only a negligible amount. The total organic carbon (TOC) and chemical oxygen demand (COD) analyses were used to assess the mineralization of CIP and PNG. The efficiency of COD and TOC removal was reached at 73.25% and 62.5% for CIP under optimized operating circumstances, and at 61.52% and 72% for PNG, respectively. These findings indicate that a sufficient rate of mineralization was obtained by SEF treatment for the mentioned pollutants. The reaction kinetics of CIP and PNG degradation by the SEF process were found to follow a pseudo-first-order kinetic model. In addition, the human health risk assessment of natural water containing CIP and PNG that was purified by US, EF, and SEF processes was done for the first time. According to the findings, the non-carcinogenic risk (HQ) caused by drinking purified water by all three systems was calculated in the acceptable range. Thus, SEF is a proper system to remove various antibiotics in potable water and reduces their human health risks.

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PURPOSE: In this study MgAl- layered double hydroxides (MgAl-LDH) nanoparticles were prepared by a simple and fast co-precipitation method and used as a catalyst in the ozonation process to degrade diazinon from aqueous solutions. METHODS: The structure of the synthesized MgAl-LDH was investigated by X-ray diffraction pattern (XRD) and field emission scanning electron microscope-energy dispersive spectroscopy (FESEM-EDX). The response surface methodology (RSM) was used to investigate the effects of different parameters including of reaction time, initial diazinon concentration, pH, and LDH dose on the removal of diazinon by MgAl-LDH catalytic ozonation process. Central Composite Design (CCD) was employed for the optimization and modeling of the process. Dispersive liquid-liquid microextraction (DLLME) method was used to extract diazinon from aqueous samples. The GC-Mass analysis was performed to determine intermediate compounds during diazinon degradation reactions. To evaluate the process performance, TOC and COD removal were measured under optimum conditions. RESULTS: The highest removal efficiency of 92% was observed in optimum conditions as follow; initial diazinon concentration: 120 mg/L, pH: 8.25, LDH dose: 750 mg/L, and reaction time: 70 min. The quadratic model was obtained with a good fit. The removal of COD and TOC were 80% and 74%, respectively. CONCLUSION: This process can be suggested and used in the treatment of various industrial wastewaters. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40201-021-00687-w.

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In the present study, SiO2-TiO2 hybrid nanomaterial and zeolite-TiO2 (Z-TiO2) composites were synthesized by the sol-gel method. Then, the antibacterial activity of the above-mentioned synthesized materials, SiO2 and zeolite (Z) was investigated by the disk diffusion method using Echerichia coli and Enterobacter aerogenes as test microorganisms. All the materials showed antibacterial activity against E. coli with 7.2, 10.7, 3.5 and 8.2 mm of inhibition zone for SiO2-TiO2 hybrid nanomaterial, SiO2, zeolite and Z-TiO2 composite, respectively. However, none of them showed antibacterial activity against E. aerogenes. The obtained results pointed out that these natural-based materials (i.e. Z, SiO2, Z-TiO2 and SiO2-TiO2), known to be noncarcinogenic and nontoxic, can be used as disinfectants against E. coli (an important indicator of the bacteriological quality of water) as safe and eco-friendly alternatives to chlorine.

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BACKGROUND: Leishmaniasis occurs with an incidence of 0.5-1.5 million new cases annually, and is also endemic in 88 countries across the world. AIM: Presently, we aimed to investigate the status of Cutaneous Leishmaniasis (CL) in Golestan Province in North of Iran. METHODS: A retrospective survey was conducted on existed data of 6873 patients with CL who attended to Health Centers in Golestan Province during 2010 to 2017 years. Data were collected using patient sheets and online registry form of CL. Descriptive statistical methods such as mean and standard deviation, and Chi-square test were employed to report and analyze results. p-Value <0.05 was considered significant. RESULTS: CL cases were more common in men 3885 (56.7%) than women 2965 (43.3%) (p = 0.001). The most and least cases was reported in 2017 and 2104 as 18 and 3 CL cases, accordingly. CL was mainly happen in the November (3816 cases), December (2832 cases) months. Presently, CL gradually increases in the last three years from 2014 to 2017 years. CONCLUSION: Decrease of exposurement, improve the nutrition and child's immunity can be more beneficial.

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In this study, a new strategy in catalytic ozonation removal method for degradation of phenol from industrial wastewater was investigated. Magnetic carbon nano composite as a novel catalyst was synthesized, characterized and then used in the catalytic ozonation process (COP) and compared with the single ozonation process (SOP). The influential parameters were all investigated. The results showed that the removal efficiency of phenol and COD (chemical oxygen demand) in COP (98.5%, 69.8%) was higher than those of SOP (78.7%, 50.5%) and the highest catalytic potential was achieved at optimal neutral pH. First order modeling demonstrated that the reactions were dependent on the concentration of catalyst, with kinetic constants varying from 0.023 1/min (catalyst = 0 g/L) to 0.071 1/min (catalyst = 4 g/L), whereby the optimum dosage of catalyst was found to be 2 g/L. Furthermore, the catalytic properties of the catalyst remained almost unchanged after 5-time reuse. The results regarding the biodegradability of the effluent showed that a 5-min reaction time in COP reduced the concentrations of phenol and COD to the acceptable levels for the efficient post-treatment in the SBR in a 4-h cycle period. Finally, this combined system is proven to be a technically effective method for treating phenolic contaminants.