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The removal of azo dye from aqueous solution by oxidation with peroxydisulfate in the presence of granular activated carbon: Performance, mechanism and reusability.

Authors :
Li, Jing
Zhu, Kangmeng
Li, Ruimeng
Fan, Xiaohui
Lin, Heng
Zhang, Hui
Source :
Chemosphere. Nov2020, Vol. 259, pN.PAG-N.PAG. 1p.
Publication Year :
2020

Abstract

Granular activated carbon (GAC) was used as catalyst for the activation of peroxydisulfate (PDS) to decolorize and degrade Acid Orange 7 (AO7) in water. EPR spectra and radical quencher experiments were employed to identify the active species for AO7 oxidation in the PDS/GAC system. Linear sweep voltammetry (LSV) and chronoamperometry test were carried out to identify the contribution of nonradical mechanism for AO7 decay. The investigation of crucial operational parameters on the decolorization indicated 100 mg/L AO7 can be almost totally decolorized in a broad range of pH. Common inorganic anions adversely affect the AO7 decolorization process and the inhibition was in the order of: HCO 3 − > H 2 PO 4 − > SO 4 2− > Cl− > NO 3 −. UV–vis spectra showed the destruction of the aromatic moiety of AO7 molecule during the oxidation reaction of the PDS/GAC system. The transformation of nitrogen related to the azo bond in AO7 molecule in this system was observed by monitoring the released N-containing inorganic ions. Recycle experiments showed GAC cannot be reused directly but its catalytic ability can be restored by using electrochemical method. Image 1 • Granular activated carbon (GAC) was an excellent activator of PDS. • AO7 was mainly decolorized by the reactive radicals produced via surface reaction. • Electron transfer from AO7 to PDS mediated by GAC also involved in AO7 removal. • The reusability of GAC can be significantly improved by electrochemical treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
259
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
145499366
Full Text :
https://doi.org/10.1016/j.chemosphere.2020.127400