4.7 Article

A newly-designed free-standing NiCo2O4 nanosheet array as effective mediator to activate peroxymonosulfate for rapid degradation of emerging organic pollutant with high concentration

Journal

CHEMOSPHERE
Volume 307, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2022.136073

Keywords

Advanced oxidation processes; Rapid degradation; Antibiotic; Activation mechanism; Nanosheet array

Funding

  1. Fundamental Research Funds for the Provincial Universities of Zhejiang [3090JYN9922001G-007]
  2. Zhejiang Provincial Natural Science Foundation of China [LY18B060003]
  3. Horizontal Subject [2022330101000174]

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The study successfully prepared a well-defined ZIF-67-derived NiCo(2)O(4) nanosheet array, which displayed great catalytic activity in the treatment of high concentration organic wastewater. The formation of nanosheet structure improved the charge transfer efficiency and resulted in excellent catalytic performance and stability.
Nowadays effective treatment of high concentration organic wastewater is still a formidable task facing human beings. Herein, for the first time, a well-defined ZIF-67-derived NiCo(2)O(4 )nanosheet array was successfully prepared by a feasible method. In comparison with ordinary NiCo2O4 nanosphere, the formation of nanosheet structure could offer more opportunities to exposure internal active sites of NiCo2O4 , thereby resulting in smaller interface resistance and higher charge transfer efficiency. As expected, ZIF-67-derived NiCo(2)O(4 )nanosheet array displayed great performance in peroxymonosulfate (PMS) activation. More importantly, recyclable redox couples of Co3+/Co2+ and Ni3+/Ni2+ endowed the stable catalytic activity of NiCo(2)O(4 )nanosheet. Interestingly, developed NiCo2O4 -1/PMS oxidation system could achieve the effective degradation of antibiotics with high con-centration in a short time. Both radical and nonradical pathways were involved into PMS activation, wherein SO4-center dot, (OH)-O-center dot, O(2)(-center dot )and O-1(2) were major reactive oxygen species. The formation paths of reactive oxygen species and effects of inorganic anions were also investigated. Electrochemical analyses revealed that NiCo2O4-1 with nanosheet structure mediated the electron transfer between PMS and tetracycline (TC), which played a vital role in TC degradation. Furthermore, developed NiCo2O4-1/PMS oxidation system displayed great removal ability towards TC in actual water samples, and degradation products were low toxicity or no toxicity. In short, current work not only developed an effective oxidation system for completing the rapid degradation of antibiotic with high concentration, but also shared some novel insights into the activation mechanism of SR-AOPs.

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