Design and modeling of diazinon degradation in hydrous matrix by Ni-doped ZnO nanorods under ultrasonic irradiation: process optimization using RSM (CCD), kinetic study, reaction pathway, mineralization, and toxicity assessment.

In first, the Ni-doped ZnO nanorods used as an appeal sonocatalyst was synthesized through co-precipitation method. Afterwards, the crystalline structure, functional groups, surface morphology, and elemental composition were characterized by a set of analysis. Removal of diazinon ((DZ) as a renowned pesticide) was investigated using sonocatalytic performance of US/Ni-doped ZnO system. In this empirical study, response surface methodology (RSM) based central composite design (CCD) was applied for optimization of operational factors. Under the optimum conditions such as initial pH = 5, initial DZ concentration = 15 mg L-1, sonocatalyst dosage = 1 g L-1, and in the presence of organic compounds (oxalic acid, humic acid, and folic acid) = 3 mg L-1, the sonocatalytic degradation of DZ after 15 min was 82.29%. The F-value (6.64) and P-value (< 0.0001) for DZ degradation in the quadratic model imply the proposed model was significant. A-factor (pH) considers as a prominent factor owing to having the highest F-value. In addition, the sonocatalytic data in this study exhibited valid fitting for the first order kinetic model (R2 > 0.98). After six consecutive cycles, the Ni-doped ZnO nanorods could be recyclable for sonocatalytic degradation of DZ. The five main compounds produced during the US/Ni-doped ZnO embracing 2-isopropyl-6-methyl-4-pyrimidinol (IMP), diethyl phosphonate, diazoxon, hydroxyldiazinon, and diazinon methyl ketone are formed in the path of DZ degradation. OFAT style also revealed 99.99% of DZ degradation with 73.26% of mineralization rate in optimum status. The Ni-doped ZnO presented agreeable sonocatalytic facility in the refinement of real water and wastewater matrix. Finally, the results of toxicity evaluation (Daphnia magna) in the sonocatalytic degradation of DZ (by US/Ni-doped ZnO system) showed that the toxicity of the DZ solution lessened under US waves (LC50 and TU 48 h equal to 36.472 and 2.741 volume percent, respectively).

Application of ZnO nanorods doped with Cu for enhanced sonocatalytic removal of Cr(VI) from aqueous solutions.

The aim of this research was to develop a simple and inexpensive process for reduction of Cr(VI) to Cr(III). Zinc oxide nanoparticles were synthesized with an easy co-precipitation procedure, and the addition of Cu2+ doping agent effectively enhanced the Cr(VI) reduction in the presence of ultrasound (US). XRD, FT-IR, FE-SEM, EDX, VSM, and XPS were used to determine the structural specifications of the zinc oxide nanoparticles. Under optimal conditions such as pH 3, initial Cr(VI) content of 20 mg/L, and catalyst dosage of 0.8 g/L, the ultrasonic/Cu-ZnO process showed a higher sonocatalytic activity (96.83%) than ultrasonic/ZnO (67.36%) after 60 min. By increasing pH and Cr(VI) concentration, the removal efficacy of Cr(VI) declined. The experimental data was well described with the first-order kinetic model. When initial Cr(VI) concentration increased from 10 to 50 mg/L, the first-order rate constant declined from 0.2326 to 0.0019 min-1 and electrical energy per order (EEO) enhanced from 19.81 to 2425.26 kWh/m3. Also, the ultrasonic/Cu-ZnO system exhibited considerable sonocatalytic performance in Cr(VI) reduction in the presence of hydrogen peroxide and citric acid, and complete removal was achieved within 60 min. The presence of anions negatively affected Cr(VI) reduction. Complete reduction was attained when ultrasound was applied at a power of 100 W. The catalyst activity was well maintained up to six consecutive cycles. In addition, the removal efficiency was approximately 62 and 65% for field water and real electroplating wastewater samples, respectively.

Enhanced electro kinetic- pseudo-Fenton degradation of pyrene-contaminated soil using Fe3O4 magnetic nanoparticles: A data set.

The aim of the data were to increase the treatment efficiency of pyrene from soil using Nano catalysts magnetite iron oxide (Fe3O4) and combined with electro kinetic. Soil provided with 100 mg/kg concentration and removal of pyrene done with EK-Fenton process. Nano catalyst was synthesized via a facile co-precipitation method and characterized by FTIR, XRD, SEM, EDX, VSM techniques. The effects of some operational parameters include catalyst dosage, pH, hydrogen peroxide concentration and the voltage were studied on the removal efficiency of pyrene. Results indicated the removal efficiency was obtained 87% under optimal conditions (pH = 3, Nano catalyst dosage= 1 g/l, H2O2=10 mM and voltage 30 V). Electrokinetic Fenton process can be as efficient and effective method for the removal of pyrene from contaminated soil using Nano Catalyst Fe3O4 introduced in optimal conditions.