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
AUTHORS (7)
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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