Electro-Fenton oxidation of Sunset Yellow FCF azo-dye in aqueous solutions
This study was designed to investigate the oxidation (decolorization/degradation) of Sunset Yellow FCF azo-dye (which is largely used as colorant in common foods and drugs industries) in aqueous solutions with electro-generated Fenton's reagent (H 2O 2/Fe 2+). This has been carried out at room...
Gespeichert in:
Veröffentlicht in: | Desalination 2011-07, Vol.274 (1), p.22-30 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | This study was designed to investigate the oxidation (decolorization/degradation) of Sunset Yellow FCF azo-dye (which is largely used as colorant in common foods and drugs industries) in aqueous solutions with electro-generated Fenton's reagent (H
2O
2/Fe
2+). This has been carried out at room temperature in an undivided electrochemical reactor of a RVC cathode and a platinum gauze anode. The progress of oxidation of Sunset Yellow FCF azo-dye by electro-generated Fenton's reagent has been monitored by UV–visible absorption, chemical oxygen demand (COD) and HPLC measurements. The results obtained under the optimal operational parameters (0.05
M Na
2SO
4 aqueous solution of pH 3 containing 0.1
mM FeSO
4 while controlling the RVC cathode applied potential at −
1.0
V vs. SCE) showed that complete decolorization (100%) and significant mineralization (approximately 97%) of Sunset Yellow FCF azo-dye have been achieved by electro-Fenton oxidation for 120
min. The rate of the oxidation reaction of Sunset Yellow FCF azo-dye in aqueous solution by electro-generated Fenton's reagent has been found to fit to pseudo first-order kinetics.
► Oxidation of Sunset Yellow until significant mineralization was achieved. ► Results indicated complete decolorization and destruction of aromatic rings. ► Rate of oxidation by electro-Fenton's reagent fits pseudo first-order kinetics. |
---|---|
ISSN: | 0011-9164 1873-4464 |
DOI: | 10.1016/j.desal.2011.01.062 |