Activation of O2 by zero-valent zinc assisted with Cu(II) for organics removal: Performance and mechanism

J Hazard Mater. 2022 Feb 15;424(Pt B):127506. doi: 10.1016/j.jhazmat.2021.127506. Epub 2021 Oct 14.

Abstract

This study proposes a method to activate O2 by accelerating the corrosion process for zero-valent zinc (ZVZ) with the assistance of Cu(II), promoting the consecutive production of reactive oxygen species. The mechanisms for reactive oxygen species generation are clarified with metronidazole (MTZ) as the targeted pollutant. The outcome suggests the association of Cu(Ⅱ) and ZVZ presents an apparent cooperative activity, an enhancement of 85% in MTZ removal is attained for the ZVZ/Cu(Ⅱ) system after 10 min compared to that for ZVZ. Analysis of the mechanisms involved indicates that this improvement is due to the addition of Cu(Ⅱ), which can accelerate the corrosion of ZVZ. In addition, quenching experiments and electron paramagnetic resonance (EPR) technology show that superoxide radicals (·O2-) result in rapid MTZ degradation. The primary component that is liable for O2 activation and a certain amount of H2O2 generation is verified to be ZVZ. Moreover, Cu(I) is detected in the ZVZ/Cu(Ⅱ) system, which arises from a direct reduction pathway driven by ZVZ and an indirect reduction pathway driven by active hydrogen atoms.

Keywords: Cu(II)/Cu(I) redox couple; H(2)O(2) generation; O(2) activation; Zero-valent zinc.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Copper
  • Electron Spin Resonance Spectroscopy
  • Hydrogen Peroxide*
  • Oxidation-Reduction
  • Reactive Oxygen Species
  • Zinc*

Substances

  • Reactive Oxygen Species
  • Copper
  • Hydrogen Peroxide
  • Zinc