Multimetallic CuCoNi Oxide Nanowires In Situ Grown on a Nickel Foam Substrate Catalyze Persulfate Activation via Mediating Electron Transfer

In situ growth of nanostructures on substrates is a strategy for designing highly efficient catalytic materials. Herein, multimetallic CuCoNi oxide nanowires are synthesized in situ on a three-dimensional nickel foam (NF) substrate (CuCoNi–NF) by a hydrothermal method and applied to peroxydisulfate...

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Published inEnvironmental science & technology Vol. 56; no. 17; pp. 12613 - 12624
Main Authors Wang, Mei-Mei, Liu, Li-Juan, Wen, Jia-Tai, Ding, Ying, Xi, Jia-Rui, Li, Jia-Cheng, Lu, Fang-Zheng, Wang, Wei-Kang, Xu, Juan
Format Journal Article
LanguageEnglish
Published Easton American Chemical Society 06.09.2022
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Summary:In situ growth of nanostructures on substrates is a strategy for designing highly efficient catalytic materials. Herein, multimetallic CuCoNi oxide nanowires are synthesized in situ on a three-dimensional nickel foam (NF) substrate (CuCoNi–NF) by a hydrothermal method and applied to peroxydisulfate (PDS) activation as immobilized catalysts. The catalytic performance of CuCoNi–NF is evaluated through the degradation of organic pollutants such as bisphenol A (BPA) and practical wastewater. The results indicate that the NF not only plays an important role as the substrate support but also serves as an internal Ni source for material fabrication. CuCoNi–NF exhibits high activity and stability during PDS activation as it mediates electron transfer from BPA to PDS. CuCoNi–NF first donates electrons to PDS to arrive at an oxidized state and subsequently deprives electrons from BPA to return to the initial state. CuCoNi–NF maintains high catalytic activity in the pH range of 5.2–9.2, adapts to a high ionic strength up to 100 mM, and resists background HCO3 – and humic acid. Meanwhile, 76.6% of the total organic carbon can be removed from packaging wastewater by CuCoNi–NF-catalyzed PDS activation. This immobilized catalyst shows promising potential in wastewater treatment, well addressing the separation and recovery of conventional powdered catalysts.
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ISSN:0013-936X
1520-5851
DOI:10.1021/acs.est.2c04312