4.7 Article

Degradation of Acid Orange 7 by peroxymonosulfate activated with the recyclable nanocomposites of g-C3N4 modified magnetic carbon

Journal

CHEMOSPHERE
Volume 205, Issue -, Pages 297-307

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2018.04.139

Keywords

Dye degradation; Peroxymonosulfate; Magnetic carbon; Graphitic carbon nitride; Advanced oxidation process

Funding

  1. National Natural Science Foundation of China [21277106]
  2. Collaborative Innovation Plan of Hubei Province for Key Technology of Eco-Ramie Industry
  3. Fund of the Key Laboratory of Catalysis and Materials Sciences of the State Ethnic Affairs Commission & Ministry of Education, South-Central University of Nationalities [CHCL13003]
  4. Scientific and Technological Innovation Plan of Wuhan Textile University

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Carbon-based catalysts have attracted high attention since they are greener and cheaper, while magnetic nanomaterials are very useful in environmental application because of the easy recovery and operation given by the magnetic separability. Therefore, graphitic carbon nitride modified magnetic carbon nanocomposites Fe3O4@C/g-C3N4 was prepared herein for the first time as a new carbon-based catalyst for the activation of peroxymonosulfate (PMS). The catalytic properties of Fe3O4@C/g-C3N4 in activating PMS for the degradation of Acid Orange 7 (AO 7), a model organic pollutant, were investigated. AO 7 degradation efficiency was significantly enhanced after modification of Fe3O4@C with g-C3N4, and the composite Fe3O4@C/g-C3N4 from loading of 5 wt% g-C3N4 and calcined at 300 degrees C for 30 min exhibited the best performance. AO 7 could be efficiently decolorized using the Fe3O4@C/C3N4 (5%) + PSM system within the pH range of 2-6, and 97% of AO 7 could be removed in 20 min without pH adjustment (pH = 4). Radical quenching and EPR studies confirmed that both sulfate and hydroxyl radicals produced from PMS activation were the active species responsible for the oxidation of AO 7. The degradation mechanism was suggested based on the experimental results and XPS analyses. It was proposed that the C=O groups on the carbon surface of Fe3O4@C rather than the C=O in g-C3N4 played a key role as the active sites for PMS activation. The catalyst was magnetically separable and displayed good stability and reusability, thus providing a potentially green catalyst for sustainable remediation of organic pollutants. (C) 2018 Elsevier Ltd. All rights reserved.

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