详细信息
Direct oxidation of antibiotic trimethoprim by unactivated peroxymonosulfate via a nonradical transformation mechanism ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Direct oxidation of antibiotic trimethoprim by unactivated peroxymonosulfate via a nonradical transformation mechanism
作者:Yang, Xuerui[1];Ding, Xi[1];Zhou, Lei[1,2];Zhao, Qing[1];Ji, Yuefei[3];Wang, Xingbao[4];Chovelon, Jean-Marc[5];Xiu, Guangli[1,2]
机构:[1]East China Univ Sci & Technol, Sch Resources & Environm Engn, State Environm Protect Key Lab Environm Risk Asse, Shanghai 200237, Peoples R China;[2]Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China;[3]Nanjing Agr Univ, Coll Resources & Environm Sci, Nanjing 210095, Peoples R China;[4]Taiyuan Univ Technol, Training Base State Key Lab Coal Sci & Technol, Jointly Constructed Shanxi Prov & Minist Sci & Te, Taiyuan 030024, Peoples R China;[5]Univ Claude Bernard Lyon 1, Univ Lyon, IRCELYON, CNRS, 2 Ave Albert Einstein, F-69626 Villeurbanne, France
年份:2021
卷号:263
外文期刊名:CHEMOSPHERE
收录:;EI(收录号:20203709160028);WOS:【SCI-EXPANDED(收录号:WOS:000595802200267)】;
基金:This work was financially supported by the National Natural Science Foundation of China (No. 21806037, 21808153, and U1810113).
语种:英文
外文关键词:Peroxymonosulfate; Trimethoprim; Stoichiometry; DFT Calculation; Antioxidant
摘要:Application of activated peroxymonosulfate (PMS) to generate sulfate radical or hydroxyl radical is a promising strategy for wastewater treatment, while our knowledge on the background reaction, namely, the direct interaction between PMS and target contaminants is quite limited. In this contribution, the degradation kinetics, stoichiometry, products and mechanism of the reaction between unactivated PMS and trimethoprim (TMP), one of the most commonly detected micro-pollutants in the aquatic system were investigated systematically. The results indicated that TMP was susceptible to degradation by direct PMS oxidation via a non-radical process. By recording the decay of two reactants simultaneously, the stoichiometric ratio between PMS and TMP was estimated to be approximately 1. Higher PMS levels exhibited a promotion effect on PMS decay. And the degradation was pH-dependent, basic conditions were favorable for TMP degradation, which could be well modeled based on the species-specific reactions. The two amine groups on the pyrimidine ring were identified as the reactive sites. After direct attacks by PMS, they would be oxidized to form hydroxylamine-products, namely, N-8-OH-TMP and N-9-OH-TMP. These two hydroxylamine-products were quite stable and resistant to further oxidation by PMS, preventing the formation of more toxic nitroso- and nitro-products. The new findings in the present work would provide beneficial information on the strategy choice for the elimination of specific pollutants, like TMP, as PMS also exhibits relatively high reactivity towards them. (C) 2020 Elsevier Ltd. All rights reserved.
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