Monochloramination of Oxytetracycline: Kinetics, Mechanisms, Pathways, and Disinfection By-Products Formation

Monochloramination of Oxytetracycline: Kinetics, Mechanisms, Pathways, and Disinfection By-Products Formation
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土霉素的一氯胺化:动力学、机制、途径和消毒副产物的形成

DOI:
10.1002/clen.201200344
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发表时间:
2013-10
影响因子:
1.7
通讯作者:
Cao Qin
Cao Qin
中科院分区:
环境科学与生态学4区
文献类型:
--
作者:
Bi Xiangyu;Bin XU;Yi-Li Lin;Chen-Yan Hu;Tao Ye;Cao Qin

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本研究考察了土霉素(OTC)一氯胺化过程中的降解动力学、消毒副产物(DBPs)的生成情况以及降解途径。降解动力学可用二级动力学模型很好地描述,第……(这里“fi”似乎不完整,你可以检查下是否有误,以便我准确翻译)
This study investigated the degradation kinetics, formation of disinfection by-products (DBPs), and degradation pathways during monochloramination of oxytetracycline (OTC). The degradation kinetics can be well described by a second-order kinetic model, first-order in monochloramine (NH2Cl), and first-order in OTC. Reaction of OTC with NH2Cl shows a high reactivity, with the apparent rate constant of 17.64/M/s at pH 7. The apparent rate constant declined as pH increased from 5 to 10. Six DBPs were detected during monochloramination of OTC, including chloroform (CF), 1,1-dichloro-2-propanone (1,1-DCP), 1,1,1-trichloro-2-propanone (1,1,1-TCP), dichloroacetonitrile (DCAN), trichloronitromethane (TCNM), and N-nitrosodimethlyamine (NDMA). CF, DCAN and NDMA had the maximum yields at neutral pH, while 1,1-DCP and 1,1,1-TCP had the maximum yields at pH 4. However, TCNM concentration increased as pH increased. Degradation pathways of OTC monochloramination were then proposed. Hydroxylation and Cl-substitution are found to be the dominant mechanisms in monochloramination of OTC.
DOI: 10.1021/ja01597a081
发表时间: 1956-08
影响因子: 15
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