Efficient degradation of N-nitrosopyrrolidine using CoFe-LDH/AC particle electrode via heterogeneous Fenton-like reaction

With the rapid development of drinking water disinfection technology, extensive attentions are paid to the nitrogenous disinfection by-products (N-DBPs) that has strong carcinogenicity, thus their degradation becomes important for the health of human beings. In this work, for the first time, CoFe-LD...

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Veröffentlicht in:Chemosphere (Oxford) 2023-02, Vol.313, p.137446, Article 137446
Hauptverfasser: Jiang, Zhuwu, Wang, Yuchang, Yu, Hai, Yao, Ning, Shen, Jyunhong, Li, Yan, Zhang, HongYu, Bai, Xue
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Sprache:eng
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Zusammenfassung:With the rapid development of drinking water disinfection technology, extensive attentions are paid to the nitrogenous disinfection by-products (N-DBPs) that has strong carcinogenicity, thus their degradation becomes important for the health of human beings. In this work, for the first time, CoFe-LDH material used as particle electrode is proposed to treat trace N-nitrosopyrrolidine (NPYR) in a three-dimensional aeration electrocatalysis reactor (3DAER). The factors on the degradation efficiency and energy consumption of NPYR are systematically investigated, and the results of radical quenching experiments show that the degradation of NPYR is completed by combining with ·OH, ·O2and direct oxidation together. CoFe-LDH particle electrode plays a vital role in generating ·OH via heterogeneous ‾Fenton-like reaction. Moreover, the adsorbed saturated CoFe-LDH particle electrode can be regenerated by electrochemical action to induce further recycle adsorption and form in-situ electrocatalysis. This work pave a way for the removal of NPYR with high efficiency, low energy conservation and environmental protection. [Display omitted] •Electrochemical catalytic oxidation of nitrogenous disinfection by-products.•CoFe-LDH/AC were prepared as novel particle electrodes.•NPYR can be effectively degraded by CoFe-LDH/AC under low energy consumption.•Degradation mechanism under 3DAER with NPYR was proposed.
ISSN:0045-6535
1879-1298
DOI:10.1016/j.chemosphere.2022.137446