62
Views
4
CrossRef citations to date
0
Altmetric
Articles

A comparison of electrolysis and Fenton reaction pretreatment methods for dye wastewater

, &
Pages 4547-4552 | Received 01 Jun 2012, Accepted 01 May 2013, Published online: 05 Jun 2013
 

Abstract

Electrochemical oxidation is an effective pretreatment method for dye wastewater. In this study, the pretreatment of actual dye wastewater by electrochemical oxidation using a Ti/PbO2 anode and a Ti/RuO2 anode were compared with the data obtained by the Fenton reaction. The optimum pH, Fe2+ dosage, and H2O2 dosage were 3.0, 400 mg/L, and 480 mg/L, respectively, for the Fenton process. The chemical oxygen demand (COD) was reduced by 26.5% by the Fenton reaction at the optimum conditions. Various densities (20–30 mA/cm2) were applied in the electrolysis process and the appropriate current density was 20 mA/cm2. The reduction in the COD and color removal increased with time, and pH fluctuations did not have a significant effect on the process. The electrolysis process was more efficient for decolorization than the Fenton process in the presence of chlorine. Among the three methods, electrocatalytic oxidation using a Ti/PbO2 anode was the most efficient method for COD removal and decolorization. At 90 min, the COD decreased by 25% and color removal was 95% with a high current efficiency of 62%.The cost of this process was 0.308 USD per kilogram reduction in the COD.

Acknowledgments

This work was financially supported by the National Key Project of Scientific and Technical Supporting Programs Funded by Ministry of Science & Technology of China (No. 2011BAE07B09).

Log in via your institution

Log in to Taylor & Francis Online

There are no offers available at the current time.

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.