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高效液相色谱-串联质谱法同时测定水体和沉积物中12种有机磷酸酯类化合物
引用本文:陈玫宏,徐怀洲,宋宁慧,吴晟旻,程杰,李江,张圣虎,石利利.高效液相色谱-串联质谱法同时测定水体和沉积物中12种有机磷酸酯类化合物[J].分析化学,2017,45(7).
作者姓名:陈玫宏  徐怀洲  宋宁慧  吴晟旻  程杰  李江  张圣虎  石利利
作者单位:1. 贵州大学资源与环境工程学院, 贵阳 550025;环境保护部南京环境科学研究所, 南京 210042;2. 环境保护部南京环境科学研究所,南京,210042;3. 国家海洋局第二海洋研究所,杭州,310012;4. 贵州大学资源与环境工程学院,贵阳,550025
基金项目:国家自然科学基金,贵州大学引进人才科研基金(No.贵大人基合字(2013)13号)资助 This work was supported by the National Natural Science Foundation of China,Research Fund on Talent Introduction of Guizhou University (No.
摘    要:建立了高效液相色谱-质谱联用技术结合固相萃取和液液萃取方法检测水体和沉积物中12种磷酸酯类(OPEs)化合物残留的方法.水样样品经HLB固相萃取柱富集,乙酸乙酯洗脱两次,沉积物样品以乙腈超声萃取,旋转蒸发至干,用超纯水稀释后重复水样处理步骤,采用ZORBAX Eclipse Plus C18色谱柱(150 mm×2.1 mm, 3.5 μm)进行分离,以0.2%甲酸-甲醇作为流动相进行梯度洗脱,采用正离子MRM监测模式,外标法定量分析.水样中,12种OPEs在0.05、0.10和0.50 μg/L加标水平下,除TMP (28.5%~47.8%)和TEHP (22.4%~73.8%) 外,其余目标化合物的平均回收率为66.4%~115.0%,相对标准偏差为0.5%~9.1%,方法定量限(MOQ)为0.001~0.050 μg/L;沉积物中,在5、10和50 μg/kg加标水平下,除TMP(35.7%~44.9%)、TCEP (31.2%~48.9%)外,其余目标化合物的平均回收率为65.9%~120.0%,相对标准偏差为0.01%~9.5%,方法定量限(MOQ)为0.02~2.0 μg/kg(dw).基于上述方法对太湖水样和沉积物样品中目标化合物定量检测分析,∑OPEs含量分别为0.1~1.7 μg/L和8.1~420 μg/kg dw.

关 键 词:有机磷酸酯  高效液相色谱-串联质谱法  水样  沉积物

Simultaneous Determination of 12 Kinds of Organophosphates inWater and Sediment by High Performance LiquidChromatography-Tandem Mass Spectrometry
CHEN Mei-Hong,XU Huai-Zhou,SONG Ning-Hui,WU Sheng-Min,CHENG Jie,LI Jiang,ZHANG Sheng-Hu,SHI Li-Li.Simultaneous Determination of 12 Kinds of Organophosphates inWater and Sediment by High Performance LiquidChromatography-Tandem Mass Spectrometry[J].Chinese Journal of Analytical Chemistry,2017,45(7).
Authors:CHEN Mei-Hong  XU Huai-Zhou  SONG Ning-Hui  WU Sheng-Min  CHENG Jie  LI Jiang  ZHANG Sheng-Hu  SHI Li-Li
Abstract:A method was developed for determination of 12 kinds of phosphate compounds in water and sediment by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) coupled with solid phase extraction (SPE) and ultrasonic extraction.The water samples were concentrated by HLB solid-phase extraction (SPE) column and eluted twice with ethyl acetate, ultrasonic solvent extraction for sediment samples and then repeated the operation of water samples after diluted with deionized water.The sample were separated on a ZORBAX Eclipse Plus C18 (150 mm × 2.1 mm, 3.5 μm) column by a gradient elution with 0.2% formic acid aqueous solution and methanol as the mobile phase.Ion mode analysis was monitored by high performance liquid chromatography mass spectrometer (MRM).The target compounds were quantified by external standard method.At the spiked levels (0.05, 0.1 and 0.5 μg/L), the average recoveries of 12 kinds of OPEs in water samples ranged from 66.4% to 115%, except for TMP (28.5%-47.8%) and TEHP (22.4%-73.8%).The relative standard deviation RSD (n=3) was 0.5%-9.09%, and the method quantification (MOQ) was 0.001-0.05 μg/L, However at the spiked levels of 5, 10 and 50 μg/kg, the average recoveries of 12 kinds of OPEs in sediment samples ranged from 65.4% to 120.0%, except for TMP (35.7%-44.9%) and TCEP (31.2%-48.9%).The relative standard deviation RSD (n=3) was 0.01%-9.54%, and the MOQ for sediment was 0.02-2.0 μg/kg dw.Based on the above methods, the detection and analysis of the targets in the water and sediments samples of Taihu Lake were carried out.The results showed that the concentrations of ΣOPEs were 0.1-1.7 μg/L and 8.1-420 μg/(kg dw), respectively.
Keywords:Organophosphate esters  High performance liquid chromatography-tandem mass spectrometry  Water samples  Sediments
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