Application of central composite design for the optimization of photodestruction of a textile dye using UV/S2O82- process

The photooxidative destruction of C. I. Basic Red 46 (BR46) by UV/S2O82- process is presented. Central Composite Design (CCD) was employed to optimize the effects of operational parameters on the photooxidative destruction efficiency. The variables investigated were the initial dye and S2O82- concentrations, reaction time and distance of the solution from UV lamp. The predicted values of the photodestruction efficiency were found to be in good agreement with the experimental values (R2 = 0.9810, Adjusted R2 = 0.9643). The results of the optimization predicted by the model showed that the maximum decolorization efficiency (>98%) was achieved at the optimum conditions of the reaction time 10 min, initial dye concentration 10 mg/l, initial peroxydisulfate concentration 1.5 mmol/l and distance of UV lamp from the solution 6 cm. The figure-of-merit electrical energy per order (EEo) was employed to estimate the electrical energy consumption and related treatment costs

Photocatalytic degradation of three azo dyes using immobilized TiO2 nanoparticles on glass plates activated by UV light irradiation: Influence of dye molecular structure

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Escherichia Coli Removal from Water Using Electrophotocatalytic Method

Electrochemical has the suitable method of drinking water disinfection. This method leads to production of hydroxyl radicals which are known powerfull oxidant agent. In recent years, water disinfection using electrophotocatalytic method is spreading. The aim of this experimental applied study is to evaluate the removal of Escherichia Coli , as the microbial contamination indicator of water, from drinking water using electrophotocatalytic method. The contaminated water in an electrophotocatalytic reactor were prepared by adding 102-103 cell of E. coli bacteria to drinking water. The studied variables were pH (6-8), the number of bacterial suspensions (102-103 cells / ml), the UV-A lamps (2-4 W), times (5-40 min), the distances between electrodes (2-3.5 cm), layering of zinc oxide nanoparticles (1-3), and voltages (10-40). The findings showed the correlation between removal of cells and UV-A lamps, voltage, and time of electrolysis. Optimal removal (MPN: 0) was obtained at pH 8, time of electrolysis: 5 minutes, 2 layer of nano ZnO, and voltage of 10 V. This result offers that this method is an efficient method for water disinfection

Improving photocatalytic activity of the ZnS QDs via lanthanide doping and photosensitizing with GO and g-C3N4 for degradation of an azo dye and bisphenol-A under visible light irradiation

In this research, insertion of Gd ions (2 wt%) into the crystalline lattice of the ZnS QDs enhanced the photocatalytic activity of the QDs. In addition, the influence of graphene oxide (GO) and graphitic carbon nitride (g-C3N4) was assessed on the photocatalytic activity of the ZnS QDs through degradation of acid red 14 (AR14) and bisphenol-A (BA) under visible light. Higher photocatalytic degradation efficiency (97.1% for AR14 and 67.4% for BA within 180 min) and higher total organic carbon (TOC) removal (67.1% for AR14 and 59.2% for BA within 5 h) was achieved in the presence of ZnS QDs/g-C3N4 compared with ZnS QDs/GO nanocomposite. Finally, the Gd-doped ZnS QDs were hybridized with g-C3N4 as optimal support to fabricate a potent visible-light-driven photocatalyst for the decomposition of organic contaminants. The maximum photocatalytic degradation of 99.1% and 80.5% were achieved for AR14 and BA, respectively, in the presence of Gd-doped ZnS QDs/g-C3N4 nanocomposite. The photosensitization mechanism was suggested for the improved photocatalytic activity of the ZnS QDs/GO, ZnS QDs/g-C3N4, and Gd-doped ZnS QDs/g-C3N4 nanocomposites under visible light. © 2022 Elsevier Lt