Electrocoagulation process for the decolorization of wastewater containing Reactive Red 195 and CFD simulation of the hydrodynamic in a continuous-flow single-channel reactor

Electrode Batch reactor 0211 other engineering and technologies 02 engineering and technology Wastewater Computational fluid dynamics Environmental technology. Sanitary engineering Biochemistry Analytical Chemistry (journal) Engineering Electrolyte Reductive Dechlorination cfsc reactor TD1-1066 Water Science and Technology Chromatography Physics Multiphysics Wastewater Decontamination cfd simulation Chemistry electrocoagulation Heterogeneous Catalysis Physical chemistry Physical Sciences Thermodynamics Advanced Oxidation Processes for Water Treatment Flow (mathematics) textile wastewater Finite element method Biomedical Engineering Environmental engineering Nanoscale Zero-Valent Iron Applications and Remediation FOS: Medical engineering Mechanics rr195 Quantum mechanics Electrolysis Environmental science Catalysis Chemical engineering Electrocoagulation Current (fluid) FOS: Chemical engineering Residence time distribution Intensity (physics) FOS: Environmental engineering Materials science Anode decolorization Effluent Environmental Science Water Treatment Wastewater Treatment
DOI: 10.2166/wpt.2023.069 Publication Date: 2023-05-04T09:19:10Z
ABSTRACT
Abstract The highly colored textile effluents require efficient treatment before being released into the environment. In this study, a continuous-flow single-channel reactor operating in closed- circuit was used to apply electrocoagulation for the treatment of synthetic textile wastewater. First, the characterization of the hydrodynamic within the reactor is evaluated by Computational Fluid Dynamics simulation using the k-ε turbulence model (Comsol Multiphysics®). Apart from a non-uniform distribution of the velocities inside the reactor, no particular anomaly was observed. Second, the decolorization efficiency was examined under various current intensities, electrolysis times, and initial dye concentrations. By operating under a current intensity of 100 mA instead of 50 mA, the required electrolysis time to achieve a decolorization efficiency of 80% decreased by 40%, while the specific electrode consumption remained slightly unchanged at about 0.19 kg Al·kg−1. At a current intensity of 100 mA and an electrolysis time of 26 min, and the increase in the initial dye concentration from 10 to 50 mg·L−1 the decolorization efficiency decreased remarkably while the specific electrode consumption was kept constant at about 0.15 kg Al·kg−1 dye removed. The knowledge obtained through this study can be used for the transposition from batch to continuous mode.
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