4.7 Article

An anode fabricated by Co electrodeposition on ZIF-8/CNTs/CF for peroxymonosulfate (PMS) activation

Journal

CHEMOSPHERE
Volume 313, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2022.137384

Keywords

Peroxymonosulfate (PMS) activation; Anode modification; The electrochemical advanced oxidation; processes (AOPs); Radical transformation; Tetracycline

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A Co@ZIF-8/CNTs-CF anode was prepared for peroxymonosulfate (PMS) activation, showing enhanced performance in tetracycline (TC) removal compared to a bare CF anode + PMS system. The enhanced activation was attributed to the high pyrrolic N content and low valence state of Co in the Co@ZIF-8/CNTs-CF anode. Quenching experiments and EPR tests revealed the generation of SO4 center dot-and reactive oxygen-containing reactive species (O2 center dot-and 1O2) during PMS activation by the anode, which contributed to TC removal. The anode for PMS activation provides a reference for wastewater treatment using electrochemical advanced oxidation processes (EAOPs).
A Co@ZIF-8/CNTs-CF anode for PMS activation was prepared by Co electrodeposition on carbon felt (CF) modified with ZIF-8 and carbon nanotubes (CNTs). The results showed that the fabricated Co@ZIF-8/CNTs-CF anode was an effective peroxymonosulfate (PMS) activator toward tetracycline (TC) removal. Compared with that in reaction system of bare CF anode + PMS, the reaction system of Co@ZIF-8/CNTs-CF anode + PMS exhibited 3.08 times decrease in the activation energy demanded and 4.21 times increase in the reaction rate constant (k), resulting in a kinetic favorable process of PMS activation by the Co@ZIF-8/CNTs-CF anode. The enhanced activation performance of the fabricated anode was ascribed to the high contents of the pyrrolic N and low valence state of Co in the Co@ZIF-8/CNTs-CF anode. Furthermore, the influence factors on the character-istics of transformation among the generated reactive species during the anodic PMS activation process were comprehensively investigated by the quenching experiments and the electron paramagnetic resonance (EPR) tests. The results showed that the SO4 center dot-and reactive oxygen-containing reactive species (O2 center dot-and 1O2) were generated during the activation of PMS by anode and became the major contributors toward TC removal. The production of 1O2 was through the dismutation of O2 center dot-. In addition, the EPR experiments demonstrated that O2 center dot- was generated mainly through the anodic PMS activation but the electrochemically driven molecular oxygen reduction reaction (ORR) process. The fabricated Co@ZIF-8/CNTs-CF anode for PMS activation provided a reference for the wastewater treatment based on the electrochemical advanced oxidation processes (EAOPs).

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