Sequestration and Degradation of Waterborne Pollutants in N-Doped Porous Carbon Decorated with Fe Single Sites

Recently, advanced oxidation processes (AOPs) based on peroxymonosulfate (PMS) have rapidly developed. However, the low concentrations of waterborne pollutants remain a significant obstacle to their effective removal. This study proposes a “sequestration-degradation” strategy, utilizing a catalyst with high adsorption and catalytic performance to enrich low-concentration waterborne pollutants from water, followed by flushing the packed column with a minimal amount of PMS solution to achieve pollutant degradation and column regeneration. Mesoporous carbon decorated with single-atom iron (FeN4/NC) was prepared and fully characterized. It demonstrated fast adsorption kinetics and a high adsorption capacity for common waterborne pollutants. Additionally, due to its high activity in PMS activation to produce singlet oxygen (1O2) and superoxide (O2•–), FeN4/NC can quickly degrade and partially mineralize 4-chlorophenol (4-CP). We indicate that FeN4/NC is a bifunctional material, with the NC support serving as the adsorption center for 4-CP, while Fe sites serve as activation centers for PMS. A proof-of-concept design for sequestration and degradation of rhodamine B was constructed using FeN4/NC, demonstrating that the current wastewater treatment approach based on the “sequestration-degradation” concept is feasible. Our findings provide a new pathway for improving the efficiency of AOPs in practical applications.

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Publication Details

Journal
ACS ES&T Engineering
Published
2025-03-05
DOI
https://doi.org/10.1021/acsestengg.5c00007
Citations
1
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.36

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article

Sequestration and Degradation of Waterborne Pollutants in N-Doped Porous Carbon Decorated with Fe Single Sites

Chen‐Ho Tung, Guanyun Zhang, Yafei Fan, Yifeng Wang et al.
1 citations
ACS ES&T Engineering
Advanced Photocatalysis Techniques
0.36
article

Sequestration and Degradation of Waterborne Pollutants in N-Doped Porous Carbon Decorated with Fe Single Sites

Chen‐Ho Tung, Guanyun Zhang, Yafei Fan, Yifeng Wang, Feifei Wang, Zhaoli Sun, Dezhi Kong, Jianfei Yao, Menghui Chu
article en
1 citations

Abstract

Recently, advanced oxidation processes (AOPs) based on peroxymonosulfate (PMS) have rapidly developed. However, the low concentrations of waterborne pollutants remain a significant obstacle to their effective removal. This study proposes a “sequestration-degradation” strategy, utilizing a catalyst with high adsorption and catalytic performance to enrich low-concentration waterborne pollutants from water, followed by flushing the packed column with a minimal amount of PMS solution to achieve pollutant degradation and column regeneration. Mesoporous carbon decorated with single-atom iron (FeN4/NC) was prepared and fully characterized. It demonstrated fast adsorption kinetics and a high adsorption capacity for common waterborne pollutants. Additionally, due to its high activity in PMS activation to produce singlet oxygen (1O2) and superoxide (O2•–), FeN4/NC can quickly degrade and partially mineralize 4-chlorophenol (4-CP). We indicate that FeN4/NC is a bifunctional material, with the NC support serving as the adsorption center for 4-CP, while Fe sites serve as activation centers for PMS. A proof-of-concept design for sequestration and degradation of rhodamine B was constructed using FeN4/NC, demonstrating that the current wastewater treatment approach based on the “sequestration-degradation” concept is feasible. Our findings provide a new pathway for improving the efficiency of AOPs in practical applications.

ACS ES&T EngineeringVol. 5(6)
Shandong University (CN), Interface (United States) (US)
Shandong Agriculture and Engineering University, National Natural Science Foundation of China, Natural Science Foundation of Shandong Province, Taishan Scholar Project of Shandong Province, Young Scientists Fund
Clean water and sanitation
Openalex Percentile: Top 46%
Advanced Photocatalysis Techniques
0.36
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