4.7 Article

Activation of peroxymonosulfate by MnO2 with oxygen vacancies: Degradation of organic compounds by electron transfer nonradical mechanism

Journal

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2022.107481

Keywords

Advanced oxidation processes; Manganese dioxide; Oxygen vacancies; Electron transfer; Peroxymonosulfate

Funding

  1. National Key Research and Development Program of China [2016YFC0400708]
  2. National Natural Science Foundation of China [51572089]
  3. Natural Science Foundation of Guangdong Province China [2019A1515011761]
  4. Foundation of Science and Technology Planning Project of Guangzhou, China [201804010398]

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Recent studies have shown that the introduction of oxygen vacancies in MnO2 materials can greatly enhance the adsorption capacity of the material for PMS, leading to the formation of more favorable reactive complexes in the electron transfer mechanism. Additionally, the V-o-MnO2/PMS system has significantly improved the degradation efficiency of pollutants, highlighting the important role of oxygen vacancies in the electron transfer mechanism and providing a new method for practical application in wastewater treatment.
Recently, ecofriendly and low toxicity manganese-based materials are receiving increased attention for the activation of peroxymonosulfate (PMS). The surface property of manganese-based materials has strong effect on its activation performance. In this study, MnO2 with differing levels of oxygen vacancies (V-o-MnO2) were prepared and used for PMS activation. The effects of oxygen vacancies (V-o), activator dosage, PMS concentration, and the initial pH on para-chloroaniline (PCA) degradation were studied. In these studies, V-o-MnO2 showed good stability and reusability for PMS activation. In addition, a series of experiments revealed the PMS activation mechanism. Interestingly, center dot OH, SO4 center dot--and O-1(2) were not primarily responsible for PCA degradation. PCA was degraded by the reactive complex formed by PMS and V-o-MnO2. Based on the characterization results and DFT calculations, the introduction of V-o in MnO2 changed the charge distribution of Mn atoms and enhanced PMS adsorption. This is more favorable to form the reactive complex in electron transfer mechanism. Besides, V-o increases the Mn3+ content in MnO2, which enhances oxidation ability of reactive complex and the efficiency of electron transfer. The degradation efficiency of pollutants in the V-o-MnO2/PMS system has been improved significantly. This study highlights the pivotal roles of V-o in electron transfer mechanism and provides a new method for the practical application in wastewater treatment.

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