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Decolorization and mineralization efficiency of the hetero-functional reactive dyes using advanced oxidation processes
The current study was aimed at the decolorization and mineralization of six newly synthesized hetero-functional (vinyl sulfone and cyanuric chloride) azo reactive dyes (D-1 to D-6) using two advanced oxidation processes (Fenton and photo-Fenton). Results showed that both oxidation mechanisms effecti...
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Published in: | Desalination and water treatment 2021-07, Vol.227, p.350-359 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The current study was aimed at the decolorization and mineralization of six newly synthesized hetero-functional (vinyl sulfone and cyanuric chloride) azo reactive dyes (D-1 to D-6) using two advanced oxidation processes (Fenton and photo-Fenton). Results showed that both oxidation mechanisms effectively mineralized the synthesized hetero-functional azo reactive dyes. However, decolorization and mineralization of dyes through photo-Fenton oxidation were more effective than Fenton oxidation. The data revealed that process parameters (pH, Fe2+ dosage, concentration of H2O2, and reaction time) greatly affect the mineralization of the selected dyes. Decolorization efficiency (98%) and chemical oxygen demand (COD) removal (78%) was obtained for the six degraded azo reactive dyes under optimum conditions; pH (3), Fe2+ concentration (20 mg/L), H2O2 (500 mg/L), and contact time (80 min) using Fenton oxidation. On the other hand, 99% decolorization and 82% COD removal was achieved for the photo-Fenton oxidation process under optimum conditions of pH (3), Fe2+ (15 mg/L), H2O2 (300 mg/L), and irradiation time (60 min) for the six hetero-functional azo reactive dyes. From the above results, it was concluded, that both oxidation processes can be effectively employed for the degradation of the six hetero-functional azo reactive dyes. |
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ISSN: | 1944-3986 1944-3986 |
DOI: | 10.5004/dwt.2021.27247 |