Abstract

In this work, the gas diffusion electrode (GDE) cathode of Vulcan XC72 carbon modified with nanoparticles of WO2.72 (WO2.72 / Vulcan XC72) was used for H2O2 electrogeneration and degradation of 350 mL of Orange II (OII) and Sunset Yellow FCF (SY) azo dyes by electro-Fenton (EF) and photoelectro-Fenton (PEF) processes with different Fe2+ initial content (1.00, 0.50 and 0.25 mmol L-1). The WO2.72 / Vulcan XC72 GDE electrolyzed approximately 3 times more H2O2 than the Vulcan XC72 GDE. Decolorizations and mineralizations of the dye solutions were more efficient at higher concentrations of Fe2+. The decolorization decay showed pseudo-first-order kinetics. The most promising decolorization results obtained at processes of WO2.72 / Vulcan XC72 cathode combined with Pt anode (100% color removal of OII and SY at 30 and 20 min of electrolysis with 1.00 mmol L-1 Fe2+, respectively). The best mineralization achieved in trials of WO2.72 / Vulcan XC72 cathode combined with boron-doped diamond (BDD) anode (82% total organic carbon (TOC) removal of OII by PEF / 1.00 after 3 h and 90% TOC removal of SY by PEF / 0.50 after 4 h). It was found that SY decolorization was faster and mineralization showed a similar yield independent of oxidized dye.

Highlights

  • The discharge of large volumes of azo dye industrial effluents into water bodies is a concerning practice because it can generate serious environmental and health problems;[1] such highly colored dyes are a dramatic source of aesthetic pollution,[2] as well as being toxic, carcinogenic[3,4] and mutagenic.[5]

  • The micrographs obtained by transmission electron microscopy (TEM) showed the dispersion and shape of the nanometer structure of the WO2.72 phase anchored on Vulcan XC72 carbon

  • The contact angle values showed that the WO2.72 / Vulcan XC72 material is more hydrophilic than pure Vulcan XC72.25

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Summary

Introduction

The discharge of large volumes of azo dye industrial effluents into water bodies is a concerning practice because it can generate serious environmental and health problems;[1] such highly colored dyes are a dramatic source of aesthetic pollution,[2] as well as being toxic, carcinogenic[3,4] and mutagenic.[5]. This cathode was combined with the Pt and BDD anodes for decolorization and mineralization of OII and SY azo dyes by EF and PEF processes.

Results
Conclusion
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