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超高效液相色谱-串联质谱法快速测定地表水中联苯胺、苦味酸、甲萘威、阿特拉津和溴氰菊酯
引用本文:张明,唐访良,徐建芬,张伟,程新良,王立群.超高效液相色谱-串联质谱法快速测定地表水中联苯胺、苦味酸、甲萘威、阿特拉津和溴氰菊酯[J].色谱,2018,36(9):866-872.
作者姓名:张明  唐访良  徐建芬  张伟  程新良  王立群
作者单位:1. 杭州市环境监测中心站, 浙江 杭州 310007; 2. 淳安县环境保护监测站, 浙江 杭州 311700
基金项目:杭州市社会发展科研攻关项目(20130533B02,20150533B08,20160533B84).
摘    要:建立了一种经简单过滤即可直接进样的超高效液相色谱-串联质谱(UPLC-MS/MS)分析方法,可快速测定地表水中联苯胺、苦味酸、甲萘威、阿特拉津和溴氰菊酯5种有机物的残留。样品经0.2 μ m针式滤头过滤除去颗粒性杂质后,进行UPLC-MS/MS分析,采用UPLC HSS T3色谱柱,2 mmol/L乙酸铵甲醇溶液和2 mmol/L乙酸铵水溶液作为流动相进行梯度洗脱,电喷雾离子源电离,正、负离子切换多反应监测模式进行定性和定量分析。5种目标化合物分别在0.10~10.0 μ g/L或1.00~100 μ g/L范围内线性关系良好,相关系数为0.996~0.999,方法的检出限为0.01~0.22 μ g/L;高、中、低3个添加水平的回收率为81.4%~113%,相对标准偏差为0.84%~14.0%。利用该方法对杭州市部分河流和水库的地表水样品进行分析,其中阿特拉津和溴氰菊酯在部分水样中有阳性检出。结果表明,该方法简便快捷、灵敏准确,适用于地表水样品中联苯胺、苦味酸、甲萘威、阿特拉津和溴氰菊酯的快速测定。

关 键 词:阿特拉津  超高效液相色谱-串联质谱  甲萘威  苦味酸  联苯胺    溴氰菊酯  
收稿时间:2018-04-23

Rapid determination of benzidine,picric acid,carbaryl, atrazine,and deltamethrin in surface water by ultra-performance liquid chromatography-tandem mass spectrometry
ZHANG Ming,TANG Fangliang,XU Jianfen,ZHANG Wei,CHENG Xinliang,WANG Liqun.Rapid determination of benzidine,picric acid,carbaryl, atrazine,and deltamethrin in surface water by ultra-performance liquid chromatography-tandem mass spectrometry[J].Chinese Journal of Chromatography,2018,36(9):866-872.
Authors:ZHANG Ming  TANG Fangliang  XU Jianfen  ZHANG Wei  CHENG Xinliang  WANG Liqun
Institution:1. Hangzhou Environmental Monitoring Central Station, Hangzhou 310007, China; 2. Chun'an Environmental Monitoring Station, Hangzhou 311700, China
Abstract:A method requiring no pre-treatment steps other than filtration, using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), has been developed and applied for the rapid determination of benzidine, picric acid, carbaryl, atrazine, and deltamethrin residues in surface water. Water samples were filtered with a 0.2-μ m syringe filter for particle removal and injected directly into the UPLC instrument. The separation was performed on a Waters Acquity UPLC HSS T3 column utilizing a gradient elution program of methanol (containing 2 mmol/L ammonium acetate) and water (containing 2 mmol/L ammonium acetate) as the mobile phases at a flow rate of 0.4 mL/min. The detection was accomplished by multiple-reaction monitoring scanning in positive/negative ion-switching electrospray ionization mode. Good linearity was observed in the range 0.10-10.0 μ g/L or 1.00-100 μ g/L for different targets with correlation coefficients of 0.996-0.999. The limits of detection (LODs) were 0.01-0.22 μ g/L. The recoveries ranged between 81.4% and 113% at three spiked levels with relative standard deviations (n=6) between 0.84% and 14.0%. The developed method was applied to the analysis of surface waters (river water and reservoir water) from Hangzhou; atrazine and deltamethrin were detected in part of the analyzed samples. This proposed method was characterized by high sensitivity and precision, extensive analytical range, and a high analytical rate, and showed suitability for the analysis of the five named pollutants in surface water.
Keywords:ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS)  benzidine  picric acid  carbaryl  atrazine  deltamethrin  water
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