Decolorization enhancement of basic fuchsin by UV/H2O2 process: optimization and modeling using Box Behnken design.

The present work deals with the optimization of basic fuchsin dye removal from an aqueous solution using the ultraviolet UV/H2O2 process. Response Surface Modeling (RSM) based on Box-Behnken experimental design (BBD) was applied as a tool for the optimization of operating conditions such as initial dye concentration (10-50 ppm), hydrogen peroxide dosage (H2O2) (10-20 mM/L) and irradiation time (60-180 min), at pH = 7.4 under ultra-violet irradiation (254 nm and 25 W intensity). Chemical oxygen demand (COD abatement) was used as a response variable. The Box-Behnken Design can be employed to develop a mathematical model for predicting UV/H2O2 performance for COD abatement. COD abatement is sensitive to the concentration of hydrogen peroxide and irradiation time. Statistical analyses indicate a high correlation between observed and predicted values (R2 > 0.98). In the BBD predictions, the optimal conditions in the UV/H2O2 process for removing 99.3% of COD were found to be low levels of pollutant concentration (10 ppm), a high concentration of hydrogen peroxide dosage (20 mM/L), and an irradiation time of 80 min.

Degradation of methyl orange using hydrodynamic Cavitation, H2O2, and photo-catalysis with TiO2-Coated glass Fibers: Key operating parameters and synergistic effects.

Advanced oxidation processes (AOPs) are eco-friendly, and promising technology for treating dye containing wastewater. This study focuses on investigating the removal of methyl orange (MO), an azo dye, from a synthetic wastewater through the use of hydrodynamic cavitation (HC), both independently and in combination with hydrogen peroxide (H2O2), as an external oxidant, as well as photocatalysis (PC) employing catalyst coated on glass fibers tissue (GFT). The examination of various operating parameters, including the pressure drop and the concentration of H2O2, was systematically conducted to optimize the degradation of MO. A per-pass degradation modelwas used to interpret and describe the experimental data. The data revealed that exclusive employment of HC using a vortex-based cavitation device at 1.5 bar pressure drop, resulted in a degradation exceeding 96 % after 100 passes, equivalent to 230 min of treatment (cavitation yield of 3.6 mg/kJ for HC), with a COD mineralization surpassing 12 %. The presence of a small amount of H2O2 (0.01 %) significantly reduced the degradation time from 230 min to 36 min (16 passes), achieving a degradation of 99.8 % (cavitation yield of 6.77 mg/kJ for HC) with COD mineralization rate twice as much as HC alone, indicating a synergistic effect of 4.8. The degradation time was further reduced to 21 min by combining HC with PC using TiO2-coated glass fibers and H2O2, (cavitation yield of 11.83 mg/kJ for HC), resulting in an impressive synergistic effect of 9.2 and COD mineralization twice as high as the HC/H2O2 system. The results demonstrate that HC based hybrid AOPs can be very effective for treating and mineralizing azo dyes in water.

Efficient solar heterogeneous photocatalytic degradation of metronidazole using heterojunction semiconductors hybrid nanocomposite, layered double hydroxides.

This study focuses on the synthesis of various nanocomposites with heterojunction structures, MgAl-LDH (LDH = layered double hydroxides) hybrid with semiconductor such as MoO3 and CuO. These solids were synthesized by co-precipitation method at constant pH and have been characterized extensively using atomic absorption spectroscopy (AAS), X-ray diffraction (XRD), Fourier transform infrared (FTIR) and transmission electron microscopy-energy dispersive X-ray (TEM-EDX) methods. The catalytic activity of nanocomposites was tested in the photocatalytic degradation under solar irradiation of emerging pollutants as the pharmaceutical metronidazole (MNZ). The experimental parameters, including initial MNZ concentration, the nature of oxide incorporate in the photocatalyst, catalyst loading were explored. All the synthesized samples showed high photocatalytic performances; the highest photocatalysis efficiency was achieved with the photocatalyst dose 1.5 g/L and initial MNZ concentration of 10 mg/L at neutral pH. The photocatalytic experimental results were fitted very well to the Langmuir-Hinshelwood model. From the obtained results the calcined LDH/semiconductors could be efficient for the photocatalytic process under solar irradiation of pharmaceuticals and may contribute in environmental remediation.