4.7 Article

Enriched nitrogen-doped carbon derived from expired drug with dual active sites as effective peroxymonosulfate activator: Ultra-fast sulfamethoxazole degradation and mechanism insight

期刊

CHEMICAL ENGINEERING JOURNAL
卷 446, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.137407

关键词

Peroxymonosulfate; Sulfamethoxazole; Nitrogen doping; Carbon catalyst; Dual active sites

资金

  1. Hainan Province Science and Technology Special Fund [ZDYF2022SHFZ094]
  2. National Natural Science Foundation of China [22166016, 21866012]
  3. Hainan Provincial Key Research and Development Program [ZDYF2020222]
  4. open-ended fund of Key Laboratory of Agro-Forestry Environmental Processes and Ecological Regulation of Hainan Province [AFEPER202101]

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A nitrogen-doped carbon material with dual active sites was developed and shown to effectively activate peroxymonosulfate and degrade sulfamethoxazole. The material exhibited excellent catalytic activity, completely removing sulfamethoxazole in a short period of time.
It's a win-win strategy to treat organic wastewater by activating peroxymonosulfate (PMS) with nitrogen-doped carbocatalysts derived from solid waste. However, the preparation of carbocatalysts with a high nitrogen content is still tricky. Herein, enriched nitrogen-doped carbon (NDC20) with dual active sites derived from expired drugs (999 cold medicine) was developed to improve PMS activation and ultra-fast sulfamethoxazole (SMX) degradation. NDC20 with high N-doping level (23.26 at %) adjusted the charge distribution of the catalyst surface, resulting in an excellent catalytic activation of PMS. Remarkably, the NDC20/PMS system fully eliminated SMX within 2 min (k(obs) = 4.912 min(-1)), which was higher than all previously reported N-doped carbon catalysts. Quenching and electron paramagnetic resonance (EPR) experiments verified that the main mechanism involved a dual nonradical pathway involving singlet oxygen (O-1(2)) and direct electron transfer (DET). Combined with theoretical calculations and in situ FTIR spectra, the exclusive role of dual active sites (pyridinic N/pyrrolic N and electron-deficient carbon atoms) was identified. An unanticipated generation pathway of O-1(2) involving electrons acquisition by dissolved oxygen to form a superoxide radical (O-2(.-)) and PMS oxidation over electron-deficient carbon atoms was revealed. Moreover, the possible pathways of SMX degradation were proposed, and the toxicity of the intermediates was anticipated. Finally, the practical application experiments demonstrated the sustainability of the catalytic activity of NDC20, which completely removed SMX after 100 h. This work provides a neoteric idea for synthesizing high-level N-doped carbocatalysts and solid waste treatment, and deepens the mechanistic understanding of PMS activation over high-level N-doped carbocatalysts.

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