Rapid analysis of trace organophosphorous pesticides in water by high performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry
文献类型:期刊论文
作者 | Pan, YH; Jin, J; Jiang, K |
刊名 | CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
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出版日期 | 2000 |
卷号 | 28期号:6页码:666-671 |
关键词 | organophosphorous pesticides high performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry drinking water |
英文摘要 | A rapid analysis of six organophosphorous pesticides (acephate, parathion-methyl, fenitrothion, quinalphos, diazinon, phoxim) was realized by the method of high performance liquid chromatography/atmospheric chemical ionization mass spectrometry( HPLC/APCIMS) on a shea reverse-phase liquid chromatographic column of 5 cm long. The identification of trace organophosphorous pesticides in water can be well completed by applying HPLC/APCIMS technique. One on-line analysis can be accomplished with only ten minutes. The in-source collision induced dissociation (CID) MS of diazinon is also discussed. Under SIR mode, the detection limits of diazinon and quinalphos are 0.09ng and 0.1ng respectively. |
WOS记录号 | WOS:000087852500002 |
源URL | [http://ir.rcees.ac.cn/handle/311016/24139] ![]() |
专题 | 生态环境研究中心_环境化学与生态毒理学国家重点实验室 |
推荐引用方式 GB/T 7714 | Pan, YH,Jin, J,Jiang, K. Rapid analysis of trace organophosphorous pesticides in water by high performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry[J]. CHINESE JOURNAL OF ANALYTICAL CHEMISTRY,2000,28(6):666-671. |
APA | Pan, YH,Jin, J,&Jiang, K.(2000).Rapid analysis of trace organophosphorous pesticides in water by high performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry.CHINESE JOURNAL OF ANALYTICAL CHEMISTRY,28(6),666-671. |
MLA | Pan, YH,et al."Rapid analysis of trace organophosphorous pesticides in water by high performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry".CHINESE JOURNAL OF ANALYTICAL CHEMISTRY 28.6(2000):666-671. |
入库方式: OAI收割
来源:生态环境研究中心
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