过氧乙酸
化学
腐植酸
降级(电信)
恶喹酸
TCEP
胺气处理
核化学
硝基
磺胺
过氧化氢
抗生素
有机化学
催化作用
生物化学
萘啶酸
磷化氢
烷基
肥料
抗生素耐药性
电信
计算机科学
作者
Jingwen Wang,Zongping Wang,Yujie Cheng,Lisan Cao,Fan Bai,Siyang Yue,Pengchao Xie,Jun Ma
出处
期刊:Water Research
[Elsevier BV]
日期:2021-05-26
卷期号:201: 117291-117291
被引量:165
标识
DOI:10.1016/j.watres.2021.117291
摘要
Sulfonamide antibiotics (SAs) are typical antibiotics and have attracted increasing concerns about their wide occurrence in environment as well as potential risk for human health. In this study, we applied a novel advanced oxidation process in SAs degradation by combining molybdenum sulfide and peracetic acid (MoS 2 /PAA). Reactive oxygen species (ROS) including HO ● , CH 3 C(O)O ● , CH 3 C(O)OO ● , and 1 O 2 were generated from PAA by MoS 2 activation and contributed to SAs degradation. The effects of initial pH, the dosages of PAA and MoS 2 , and humic acid for SAs degradation were further evaluated by selecting sulfamethoxazole (SMX) as a target SA in the MoS 2 /PAA process. Results suggested that the optimum pH for SMX removal was 3, where the degradation efficiency of SMX was higher than 80% after reaction for 15 min. Increasing PAA (0.075–0.45 mM) or MoS 2 (0.1–0.4 g/L) dosages facilitated the SMX degradation, while the presence of humic acids retarded the SMX removal. This MoS 2 /PAA process also showed good efficiencies in removing other SAs including sulfaguanidine, sulfamonomethoxine and sulfamerazine. Their possible degradation pathways were proposed based on the products identification and DFT calculation, showing that apart from the oxidation of amine groups to nitro groups in SAs, MoS 2 /PAA induced SO 2 extrusion reaction for SAs that contained six-membered heterocyclic moieties.
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