Composite wastewater treatment by aerated electrocoagulation and modified peroxi-coagulation processes
Treatment of composite wastewater generating from the industrial estates is a great challenge. The present study examines the applicability of aerated electrocoagulation and modified peroxi-coagulation processes for removing color and COD from composite wastewater. Iron plates were used as anodes an...
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Veröffentlicht in: | Chemosphere (Oxford) 2018-08, Vol.205, p.587-593 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Treatment of composite wastewater generating from the industrial estates is a great challenge. The present study examines the applicability of aerated electrocoagulation and modified peroxi-coagulation processes for removing color and COD from composite wastewater. Iron plates were used as anodes and cathodes in both electrochemical processes and experiments were carried out in a working volume of 2 L. Aeration enhanced the efficiency of electrocoagulation process significantly. More than 50% of COD and 60% of color were removed after 1 h of electrocoagulation process operated at pH 3 and applied voltage of 1 V. Efficiency of the modified peroxi-coagulation process was significantly higher than that of aerated electrocoagulation. COD and color removal efficiencies of the modified peroxi-coagulation process were found as 77.7% and 97%, respectively after 1 h of electrolysis operated at 1 V, solution pH 3 and 50 mM hydrogen peroxide addition. This improved efficiency of modified peroxi-coagulation compared to aerated electrocoagulation is mainly due to the attack of in-situ generated hydroxyl radicals.
•Electrochemical treatment of composite wastewater.•Enhanced performance of electrocoagulation with external aeration.•Superior performance of modified peroxi-coagulation process than aerated electrocoagulation process.•Active chlorine generation is irrespective of process and pH.•Hydroxyl radicals are superior oxidant responsible for pollutant removal. |
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ISSN: | 0045-6535 1879-1298 |
DOI: | 10.1016/j.chemosphere.2018.04.141 |