中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Hydrolysis and Photodegradation of Trifloxystrobin in Aqueous Solution

文献类型:期刊论文

作者Liu, H. J. ; Zhang, X. ; Wang, H. L. ; Guo, B. Y. ; Zheng, L. ; Li, J. Z. H.
刊名ASIAN JOURNAL OF CHEMISTRY
出版日期2014
卷号26期号:10页码:2834-2838
ISSN号0970-7077
关键词Trifloxystrobin Hydrolysis Photolysis
中文摘要Hydrolysis of triffoxystrobin was investigated in pH 4-10 aqueous solutions at 25, 40 and 50 degrees C. Its photochemical experiments in acidic, neutral, alkaline solutions and 1-10 mg/L humic acid solutions were conducted. Trifloxystrobin hydrolytic rate was first-order with respect to hydroxide ion concentration. For each 10 temperature rising, the rate constant for hydrolysis increased 2-4 times. The photolytic T-1/2 of trifloxystrobin at pH 4, 7 and 9 was 13.0, 11.9 and 4.3 h, respectively. In the 1-10 mg/L humic acid solutions, the photodegradation rate constants corrected for light screening of trifloxystrbin were 0.0592-0.0577 h(-1), basically decreasing with the humic acid concentration increasing. It was concluded that in the aqueous solution, the key nucleophilic reaction partner was hydroxyl ions. Raise of temperature could accerlate hydrolysis of trifloxystrobin. The hydrolysis could accelerate the photolysis of trifloxystrobin and light screening had an effect on the photodegradation rate constants of trifloxystrobin.
WOS记录号WOS:000337769300005
公开日期2015-03-26
源URL[http://ir.rcees.ac.cn/handle/311016/9663]  
专题生态环境研究中心_中国科学院环境生物技术重点实验室
推荐引用方式
GB/T 7714
Liu, H. J.,Zhang, X.,Wang, H. L.,et al. Hydrolysis and Photodegradation of Trifloxystrobin in Aqueous Solution[J]. ASIAN JOURNAL OF CHEMISTRY,2014,26(10):2834-2838.
APA Liu, H. J.,Zhang, X.,Wang, H. L.,Guo, B. Y.,Zheng, L.,&Li, J. Z. H..(2014).Hydrolysis and Photodegradation of Trifloxystrobin in Aqueous Solution.ASIAN JOURNAL OF CHEMISTRY,26(10),2834-2838.
MLA Liu, H. J.,et al."Hydrolysis and Photodegradation of Trifloxystrobin in Aqueous Solution".ASIAN JOURNAL OF CHEMISTRY 26.10(2014):2834-2838.

入库方式: OAI收割

来源:生态环境研究中心

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