4.7 Article

Enhanced electro-oxidation/peroxone (in situ) process with a Ti-based nickel-antimony doped tin oxide anode for phenol degradation

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 384, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2019.121398

Keywords

Electro-Oxidation; In situ electro-peroxone; Nickel-antimony doped tin oxide; Phenol

Funding

  1. National Natural Science Foundation of China [21373022, 51678020, 51761145047]
  2. Opening Project of National Engineering Laboratory for Advanced Municipal Wastewater Treatment and Reuse Technology

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Recently, a novel proof-of-concept oxygen reduction reaction (ORR) based electro-oxidation (EO) process has been developed, which was accomplished by integrating anodic electrochemical oxidation coupled with an in situ electro-peroxone process, by harnessing the anodic by-product O-3 reacted with ORR cathode generated H2O2. To further enhance EO coupled in situ electro-peroxone, a nickel and antimony doped tin oxide anodic catalyst layer, namely NATO, was fabricated on Ti mesh to improve anodic oxidation and reinforce the generation of O-3, thus promoting in situ Electro-peroxone. As a result, O-3 generation rate was enhanced by 12.6%. Complete phenol, as a model organic compound, and 95% of TOC removal were achieved, respectively, during ORR-EO. Through kinetics and instrument analysis, results show that the amount of intermediates accumulated during phenol degradation was much less in this Ti/NATO based ORR-EO system than in a traditional EO system. Moreover, 35.7% of the energy consumption was saved for ORR-EO, owing to its reduced applied voltage and the enhanced in situ electro-peroxone process.

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