Enhanced conversion of superoxide radical to singlet oxygen in peroxymonosulfate activation by metal-organic frameworks derived heteroatoms dual-doped porous carbon catalyst.

Autor: Xie, Jinling1 (AUTHOR), Pan, Xiaofang1 (AUTHOR), Jiang, Chenming1 (AUTHOR), Zhao, Li1 (AUTHOR), Gong, Xiaobo1,2,3,4 (AUTHOR) gxb@sicnu.edu.cn, Liu, Yong1,2,3,4 (AUTHOR)
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Zdroj: Environmental Research. Nov2023:Part 1, Vol. 236, pN.PAG-N.PAG. 1p.
Abstrakt: The activation of persulfate technology using carbon-based materials doped with heteroatoms has been extensively researched for the elimination of refractory pollutants in wastewater. In this study, metal-organic frameworks were utilized as precursors to synthesize P, N dual-doped carbon material (PNC), which was employed to activate peroxymonosulfate (PMS) for the degradation of tetracycline hydrochloride (TCH). The results demonstrated a 90.2% removal efficiency of total organic carbon within 60 min. The significant increase of surface defects on the nitrogen self-doped porous carbon materials anchored with phosphorus promoted the conversion of superoxide radical to singlet oxygen during PMS activation, which was identified as the key active species of PNC/PMS system. Additionally, the enhanced direct electron transfer also facilitated the degradation of TCH. Consequently, TCH was successfully degraded into nontoxic and harmless inorganic small molecules. The findings of this research provide valuable insights into improving the performance of heteroatom-doped carbon materials for pollutant degradation by activating PMS and transforming the non-radical pathway. The results highlight the potential of metal-organic frameworks derived heteroatoms dual-doped porous carbon catalysts for the development of advanced treatment technologies in wastewater treatment. [Display omitted] • N, P dual-doped porous carbon catalyst was successfully derived from ZIF-8. • PNC showed excellent stability and catalysis to degrade TCH by activating PMS. • P-doped carbon catalyst promoted the conversion of O 2 ·- to 1O 2. • The efficient TCH degradation was mainly by 1O 2 and non-radical pathway in PNC/PMS system. • PNC/PMS/membrane system was successfully constructed for degradation of TCH. [ABSTRACT FROM AUTHOR]
Databáze: GreenFILE
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