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Author:

Zhao, B.-H. (Zhao, B.-H..) | Zhu, Y.-H. (Zhu, Y.-H..) | Wang, C. (Wang, C..)

Indexed by:

Scopus SCIE

Abstract:

Industrial solid waste can be used as nanoparticles potential supports to form heterogeneous catalysts for removing organic substances. Herein, coal gangue was modified by sulfuric acid pickling and high-temperature calcination, and FeCo2O4/modified coal gangue (FC-MCG) catalysts were synthesized via a citric acid combustion method. The crystal structures, surface morphology and elemental valence of the synthesized composites were investigated. The 20% FC-MCG possessed higher catalytic performance for HA degradation than other composites, achieving almost 85% degradation efficiency of HA (20 mg/L) in the presence of PMS. The fluorescence EEMs and FTIR spectra revealed the effective destruction of HA structure after reaction in the 20% FC-MCG/PMS system. Electron paramagnetic resonance (EPR) tests and quenching experiments showed that the SO4·-, •OH and 1O2 were produced in the PMS activation process. Additionally, the 20% FC-MCG catalyst still kept excellent catalytic performance after four times repeated use. This study was a meaningful exploration for conversion of industrial solid waste to high effective catalyst for wastewater treatment. © 2023 Elsevier B.V.

Keyword:

Activation mechanism Coal gangue Humic acid Peroxymonsulfate FeCo2O4

Author Community:

  • [ 1 ] [Zhao B.-H.]Department of Municipal Engineering, Beijing University of Technology, Beijing, 100124, China
  • [ 2 ] [Zhu Y.-H.]State Key Laboratory of Water Resources Protection and Utilization in Coal Mining, Beijing, 100037, China
  • [ 3 ] [Zhu Y.-H.]Department of Municipal Engineering, Beijing University of Technology, Beijing, 100124, China
  • [ 4 ] [Wang C.]Department of Municipal Engineering, Beijing University of Technology, Beijing, 100124, China

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Source :

Inorganic Chemistry Communications

ISSN: 1387-7003

Year: 2023

Volume: 152

3 . 8 0 0

JCR@2022

ESI Discipline: CHEMISTRY;

ESI HC Threshold:20

Cited Count:

WoS CC Cited Count: 0

SCOPUS Cited Count: 7

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 4

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