Catalytic ozonation of nitroimidazole antibiotics using nano-magnesium hydroxide as heavy-metals free catalyst
Sun, Q; Zhu, GC; Wu, J; Lu, J; Zhang, ZH
发表期刊DESALINATION AND WATER TREATMENT
ISSN1944-3994
2019-09
卷号161页码:216-227
关键词Nano-scale magnesium hydroxide Nitroimidazole antibiotics Catalytic ozonation Degradation
研究领域Engineering, Chemical ; Water Resources
DOI10.5004/dwt.2019.24277
产权排序[Sun, Qi; Zhu, Guangcan] Southeast Univ, Sch Energy & Environm, Nanjing 210096, Jiangsu, Peoples R China; [Wu, Jun; Zhang, Zhenhua] Ludong Univ, Sch Resources & Environm Engn, Yantai 264025, Shandong, Peoples R China; [Lu, Jian] Chinese Acad Sci, Yantai Inst Coastal Zone Res YIC, CAS Key Lab Coastal Environm Proc & Ecol Remediat, Yantai 264003, Shandong, Peoples R China; [Lu, Jian] YICCAS, Shandong Key Lab Coastal Environm Proc, Yantai 264003, Shandong, Peoples R China
作者部门海岸带环境过程实验室
英文摘要In this study, nano-magnesium hydroxide (nano-Mg(OH)(2)) was prepared and first applied for the catalytic ozonation of the widely used nitroimidazole antibiotics. Most of nitroimidazole antibiotics were rapidly removed within 10 min. The removal rate constant of metronidazole in the catalytic ozonation treatment was four times higher than that without catalyst. Persistent high catalytic activity of nano-Mg(OH)(2) maintained after three runs. The severe inhibition of hydroxyl radical scavenger (TBA) on the catalytic ozonation suggested that hydroxyl radical reaction served as the predominant process. The removal of nitroimidazole antibiotics followed a pseudo-first order kinetic model. Increase in the dosage of catalyst and reaction temperature within certain range could enhance the degradation of metronidazole, tinidazole, and dimetridazole while increase in the initial concentration of nitroimidazole antibiotics led to the decrease in the removal efficiency. All anions (Cl-, HCO3, and SO42-) and cations (Ca2+ and Mg2+) had negative influence on the removal efficiency of nitroimidazole antibiotics. Due to the unique features such as low cost and heavy-metals free, high efficiency and persistent high catalytic activity of the nano-Mg(OH)(2) in the catalytic ozonation of nitroimidazole antibiotics demonstrated that nano-Mg(OH)(2) is a promising environment-friendly ozonation catalyst in terms of antibiotic removal.
文章类型Article
资助机构National Natural Science Foundation of ChinaNational Natural Science Foundation of China [41877131, 51578132] ; One Hundred Talents Program of Chinese Academy of SciencesChinese Academy of Sciences [Y629041021] ; Taishan Scholar Program of Shandong Province [tsqn201812116] ; Two-Hundred Talents Plan of Yantai [Y739011021]
收录类别SCI
语种英语
关键词[WOS]WASTE-WATER ; 2,4-DICHLOROPHENOXYACETIC ACID ; PHOTOCATALYTIC DEGRADATION ; AQUATIC ENVIRONMENT ; INORGANIC-COMPOUNDS ; AQUEOUS-SOLUTION ; RATE CONSTANTS ; REMOVAL ; OZONE ; SULFAMETHOXAZOLE
研究领域[WOS]Engineering, Chemical ; Water Resources
WOS记录号WOS:000472928900021
引用统计
被引频次:8[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.yic.ac.cn/handle/133337/24877
专题中国科学院海岸带环境过程与生态修复重点实验室_海岸带环境过程实验室
中国科学院海岸带环境过程与生态修复重点实验室
作者单位1.Southeast Univ, Sch Energy & Environm, Nanjing 210096, Jiangsu, Peoples R China;
2.Ludong Univ, Sch Resources & Environm Engn, Yantai 264025, Shandong, Peoples R China;
3.Chinese Acad Sci, Yantai Inst Coastal Zone Res YIC, CAS Key Lab Coastal Environm Proc & Ecol Remediat, Yantai 264003, Shandong, Peoples R China;
4.YICCAS, Shandong Key Lab Coastal Environm Proc, Yantai 264003, Shandong, Peoples R China
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GB/T 7714
Sun, Q,Zhu, GC,Wu, J,et al. Catalytic ozonation of nitroimidazole antibiotics using nano-magnesium hydroxide as heavy-metals free catalyst[J]. DESALINATION AND WATER TREATMENT,2019,161:216-227.
APA Sun, Q,Zhu, GC,Wu, J,Lu, J,&Zhang, ZH.(2019).Catalytic ozonation of nitroimidazole antibiotics using nano-magnesium hydroxide as heavy-metals free catalyst.DESALINATION AND WATER TREATMENT,161,216-227.
MLA Sun, Q,et al."Catalytic ozonation of nitroimidazole antibiotics using nano-magnesium hydroxide as heavy-metals free catalyst".DESALINATION AND WATER TREATMENT 161(2019):216-227.
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