Activation of peroxymonosulfate by morphologically modified NiCo2O4 and application to diclofenac degradation

Water pollution caused by pharmaceutical wastewater is becoming increasingly serious. Diclofenac (DCF), a pharmaceutical compound widely used in many medicines, is an organic pollutant that poses potential risks to ecosystems and human health. In this study, a morphologically modified NiCo 2 O 4 (NCO) catalyst was synthesized via a hydrothermal method and employed to activate peroxymonosulfate (PMS) for DCF degradation. As a result, 99.9 % of the DCF was successfully degraded within 10 min. It also succeeded in mineralizing 97.2 % of DCF after 10 min. Moreover, the NCO/PMS system was effective over a wide pH range. The degradation pathways involved both radical and non-radical mechanisms, with 1 O 2 , SO 4 •– , and • OH identified as the primary active species. In addition, the surface hydroxyl groups on the NCO are likely to play a significant role in the degradation process. This paper presents the development of a highly efficient catalyst for the degradation of organic pollutants using PMS. • A morphologically modified NCO catalyst was prepared via hydrothermal method. • The optimized NCO/PMS could degrade 99.9 % and mineralize 97.2 % of DCF in 10 min. • 1 O 2 , SO 4 •– , and •OH were the main reactive species in the degradation reaction. • Surface hydroxyl groups on NCO were important for the formation of SO 4 •– and 1 O 2 . • Stable redox couple ratios in NCO indicate good redox cycles during the reaction.

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Publication Details

Journal
Next Materials
Published
2025-03-29
DOI
https://doi.org/10.1016/j.nxmate.2025.100597
Citations
3
Primary Topic
Advanced oxidation water treatment
Type
article
Field-Weighted Citation Impact
2.45

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article

Activation of peroxymonosulfate by morphologically modified NiCo2O4 and application to diclofenac degradation

Mai Furukawa, Satoshi Kaneco, Hideyuki Katsumata, Ikki Tateishi et al.
3 citations
Next Materials
Advanced oxidation water treatment
2.45
article

Activation of peroxymonosulfate by morphologically modified NiCo2O4 and application to diclofenac degradation

Mai Furukawa, Satoshi Kaneco, Hideyuki Katsumata, Ikki Tateishi, Kanon Sampe
article en
3 citations

Abstract

Water pollution caused by pharmaceutical wastewater is becoming increasingly serious. Diclofenac (DCF), a pharmaceutical compound widely used in many medicines, is an organic pollutant that poses potential risks to ecosystems and human health. In this study, a morphologically modified NiCo 2 O 4 (NCO) catalyst was synthesized via a hydrothermal method and employed to activate peroxymonosulfate (PMS) for DCF degradation. As a result, 99.9 % of the DCF was successfully degraded within 10 min. It also succeeded in mineralizing 97.2 % of DCF after 10 min. Moreover, the NCO/PMS system was effective over a wide pH range. The degradation pathways involved both radical and non-radical mechanisms, with 1 O 2 , SO 4 •– , and • OH identified as the primary active species. In addition, the surface hydroxyl groups on the NCO are likely to play a significant role in the degradation process. This paper presents the development of a highly efficient catalyst for the degradation of organic pollutants using PMS. • A morphologically modified NCO catalyst was prepared via hydrothermal method. • The optimized NCO/PMS could degrade 99.9 % and mineralize 97.2 % of DCF in 10 min. • 1 O 2 , SO 4 •– , and •OH were the main reactive species in the degradation reaction. • Surface hydroxyl groups on NCO were important for the formation of SO 4 •– and 1 O 2 . • Stable redox couple ratios in NCO indicate good redox cycles during the reaction.

Next MaterialsVol. 8
Mie University (JP)
Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science
Openalex Percentile: Top 13%
Advanced oxidation water treatment
2.45
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Activation of peroxymonosulfate by morphologically modified NiCo2O4 and application to diclofenac degradation — Mai Furukawa, Satoshi Kaneco, et al. · Next Materials (2025) | TGRS Research Map | TGRS