Issue 60, 2021, Issue in Progress

Enhancing the activation of persulfate using nitrogen-doped carbon materials in the electric field for the effective removal of p-nitrophenol

Abstract

Degradation of nonbiodegradable organic compounds into harmless substances is one of the main challenges in environmental protection. Electrically-activated persulfate process has served as an efficient advanced oxidation process (AOP) to degrade organic compounds. In this study, we synthesized three nitrogen-doped carbon materials, namely, nitrogen-doped activated carbon plus graphene (NC), and nitrogen-doped activated carbon (NAC), nitrogen-doped graphene (NGE), and three nitrogen-doped carbon material-graphite felt (GF) cathodes. The three nitrogen-doped carbon materials (NC, NGE, NAC) were characterized using X-ray diffraction, Raman spectroscopy, X-ray electron spectroscopy, and nitrogen desorption–adsorption. The electron spin resonance technique was used to identify the presence of hydroxyl radicals (˙OH), sulfate radicals (SO4˙) and singlet oxygen (1O2) species. The results showed that NC was more conducive for the production of free radicals. In addition, we applied NC-GF to an electro-activated persulfate system with the degradation of p-nitrophenol and investigated its performance for contaminant degradation under different conditions. In general, the nitrogen-doped carbon electrode electro-activated persulfate process is a promising way to treat organic pollutants in wastewater.

Graphical abstract: Enhancing the activation of persulfate using nitrogen-doped carbon materials in the electric field for the effective removal of p-nitrophenol

Article information

Article type
Paper
Submitted
06 Sep 2021
Accepted
05 Nov 2021
First published
25 Nov 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 38003-38015

Enhancing the activation of persulfate using nitrogen-doped carbon materials in the electric field for the effective removal of p-nitrophenol

M. Tang and Y. Zhang, RSC Adv., 2021, 11, 38003 DOI: 10.1039/D1RA06691A

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