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Fe confined in Prophyrin-based porous organic polymer as an efficient periodate activator for nonradical pathway removal of contaminants  ( SCI-EXPANDED收录 EI收录)   被引量:4

文献类型:期刊文献

英文题名:Fe confined in Prophyrin-based porous organic polymer as an efficient periodate activator for nonradical pathway removal of contaminants

作者:Shi, Zhenyu[1] Zhang, Wei[2] Qin, Chao[1] Yan, Yan[1] Gao, Zhanqi[1] Zhu, Liang[2] Tang, Chunmei[3] Jin, Can[4] Yang, Shaogui[5]

第一作者:Shi, Zhenyu

通信作者:Gao, ZQ[1];Jin, C[2];Yang, SG[3]

机构:[1]Environm Monitoring Ctr Jiangsu Prov, Nanjing 210036, Peoples R China;[2]Hohai Univ, Coll Environm, Nanjing 210098, Peoples R China;[3]Hohai Univ, Coll Sci, Nanjing 210098, Peoples R China;[4]Chinese Acad Forestry, Inst Chem Ind Forest Prod, Key Lab Biomass Energy & Mat Jiangsu Prov, Nanjing 210042, Peoples R China;[5]Nanjing Normal Univ, Sch Environm, Nanjing 210023, Peoples R China

年份:2023

卷号:317

外文期刊名:SEPARATION AND PURIFICATION TECHNOLOGY

收录:;EI(收录号:20230076811);Scopus(收录号:2-s2.0-85152723481);WOS:【SCI-EXPANDED(收录号:WOS:000984172900001)】;

基金:This work was supported by the National Natural Science Foundation of China (42007325) .

语种:英文

外文关键词:Periodate activation; Bisphenol A; Singlet oxygen; Nonradical oxidation

摘要:Developing efficient and stable catalysts for periodate (PI) activation is important for the abatement of emerging contaminants. Herein, Fe doped into polyprophyrin-based porous organic polymer (Fe@PrPOP) was prepared via a facile one-step reaction, and its catalytic capacity and reaction mechanism for PI activation were systematically investigated. Complete removal of bisphenol A (BPA) was achieved within 12 min under the Fe@PrPOP/PI system within a wide pH range (3-8), as well as no leaching of Fe was observed throughout the reaction. Nonradical pathways, including 1O2 and electron transfer, were identified for the BPA removal. According to substantial characterizations and density functional theory calculations, we concluded that the scattered Fe species on the surface of Fe@PrPOP were the main active sites, which was conducive to the adsorption and activation of PI. In addition, the Fe@PrPOP/PI system exhibited selective oxidation toward various organic pollutants with electron-rich moieties. Overall, this study provides a promising alternative in activating PI for the removal of organic compounds in water.

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