Journal
ACS OMEGA
Volume 6, Issue 41, Pages 27288-27296Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsomega.1c04090
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The study replaced Fe(II) with Cr(VI) in Fenton-like oxidation for the degradation of Methylene Blue dye, which eliminated the limitations of classical Fenton oxidation, such as narrow working pH range and iron sludge formation. The Cr(VI)-mediated Fenton oxidation has a pH range of 3-10, and no sludge formation was observed up to four cycles, with the oxidation remaining in the pure solution phase. The complete mineralization of dye was confirmed through spectrophotometer and cyclic voltammetry analysis, with optimal performance achieved through investigation of various reaction parameters.
Fe(II)-mediated Fenton process is commonly employed for oxidative degradation of recalcitrant pollutants in wastewater. However, the method suffers from limitations like narrow working pH range and iron sludge formation. The present work deals with the degradation of Methylene Blue (MB) dye using Fenton-like oxidation by replacing Fe(II) with Cr(VI), which eliminates the limitations of classical Fenton oxidation. The Fenton-like oxidation of MB is brought about by HO center dot radicals generated by the disproportionation of chromium-coordinated peroxo complexes. It was observed that the working pH range for the Cr(VI)-mediated Fenton oxidation was 3-10, and no sludge formation takes place up to four cycles as the oxidation remains in the pure solution phase. The complete mineralization of dye was confirmed by observing the decay of MB peaks by a spectrophotometer and cyclic voltammetry. The reaction parameters like pH of the solution, temperature, degradation time, concentrations of H2O2, Cr(VI), and MB were studied for optimal performance of the Cr(VI) as the catalyst. Kinetic studies revealed that the Cr(VI)-mediated Fenton reaction follows pseudo-first-order reaction kinetics and depends on the concentration of HO center dot radicals. The proposed Cr(VI)-mediated Fenton oxidation in the present work is best suited for the degradation of organic dyes by adding H2O2 as a precursor in chromate-contaminated wastewaters.
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