4.8 Article

Ultrahigh Peroxymonosulfate Utilization Efficiency over CuO Nanosheets via Heterogeneous Cu(III) Formation and Preferential Electron Transfer during Degradation of Phenols

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 56, Issue 12, Pages 8984-8992

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c01968

Keywords

persulfate activation; high-valent copper; oxidant utilization efficiency; heterogeneous catalysis

Funding

  1. National Natural Science Foundation of China [21876108, 22106104, 22111530110, 52070128]
  2. National Institute of Environmental Health Sciences of the National Institutes of Health, USA [P42ES027725]
  3. NSF ERC on Nanotechnology-Enabled Water Treatment [EEC-1449500]

Ask authors/readers for more resources

Activation of persulfate by copper-based catalysts helps to efficiently utilize persulfate and remove organic pollutants, with high-valent copper playing a critical role. Experimental evidence shows that high-valent copper directly oxidizes phenolic pollutants, making the persulfate utilization pathway more efficient.
In persulfate activation by copper-based catalysts, high-valent copper (Cu(III)) is an overlooked reactive intermediate that contributes to efficient persulfate utilization and organic pollutant removal. However, the mechanisms underlying heterogeneous activation and enhanced persulfate utilization are not fully understood. Here, copper oxide (CuO) nanosheets (synthesized with a facile precipitation method) exhibited high catalytic activity for peroxymonosulfate (PMS) activation with 100% 4-chlorophenol (4-CP) degradation within 3 min. Evidence for the critical role of surface-associated Cu(III) on PMS activation and 4-CP degradation over a wide pH range (pH 3-10) was obtained using in situ Raman spectroscopy, electron paramagnetic resonance, and quenching tests. Cu(III) directly oxidized 4-CP and other phenolic pollutants, with rate constants inversely proportional to their ionization potentials. Cu(III) preferentially oxidizes 4-CP rather than react with two PMS molecules to generate one molecule of O-1(2), thus minimizing this less efficient PMS utilization pathway. Accordingly, a much higher PMS utilization efficiency (77% of electrons accepted by PMS ascribed to 4-CP mineralization) was obtained with CuO/PMS than with a radical pathway-dominated Co3O4/PMS system (27%) or with the O-1(2) pathway-dominated alpha-MnO2/PMS system (26%). Overall, these results highlight the potential benefits of PMS activation via heterogeneous high-valent copper oxidation and offer mechanistic insight into ultrahigh PMS utilization efficiency for organic pollutant removal.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available