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高效液相色谱-串联质谱法快速灵敏分析废水中的六种多环芳烃。

High performance liquid chromatography-tandem mass spectrometry for rapid and sensitive analysis of six polycyclic aromatic hydrocarbons in wastewater.

机构信息

Key Laboratory of Northwest Water Resource, Environment and Ecology, MOE, Xi'an University of Architecture and Technology, Xi'an 710055, China.

出版信息

Water Sci Technol. 2011;64(2):477-84. doi: 10.2166/wst.2011.710.

Abstract

A sensitive and fast method was developed to quantitatively analyse the six polycyclic aromatic hydrocarbons (fluoranthene (FLT), benzo[b]fluoranthene (BbF), benzo[k]fluoranthene (BkF), benzo[a] pyrene (Bap), benzo[ghi]perylene (BghiP) and indeno[1,2,3-cd]pyrene (INPY)) by high performance liquid chromatography (UPLC) coupling with tandem mass spectrometry (MS/MS). Chromatographic separation was performed on a Waters Acquity UPLC BEHC18 column (1.7 microm, 2.1 mm x 50 mm). A 0.2 microm precolumn filter was used to protect the analytical column. Mobile phase Awas acetonitrile containing 0.5% toluene. Mobile phase B was water. Linearity of detection was in the range of 1-100 microg L(-1); LOD of 5 PAHs were lower than 0.1 microg L(-1); LOQ were 0.2 microg L(-1) except for benzo[k]fluoranthene. The LOD and the LOQ of benzo[k]fluoranthene were respectively 0.1 microg L(-1) and 0.8 microg L(-1). Wastewater samples collected from two wastewater treatment plants were determined using this method respectively. Recovery of all compounds varied from 67.8 +/- 10.6% to 113.2 +/- 7.2%. In comparison with the existing methods, this rapid method saves time and solvent and improves instrument sample throughput by 2-5 fold.

摘要

建立了一种灵敏、快速的高效液相色谱-串联质谱法同时测定水中六种多环芳烃(荧蒽(FLT)、苯并[b]荧蒽(BbF)、苯并[k]荧蒽(BkF)、苯并[a]芘(Bap)、苯并[ghi]苝(BghiP)和茚并[1,2,3-cd]芘(INPY))的分析方法。色谱分离在 Waters Acquity UPLC BEHC18 柱(1.7μm,2.1mm×50mm)上进行,采用 0.2μm 预柱过滤器保护分析柱。流动相 A 为含 0.5%甲苯的乙腈,流动相 B 为水。检测线性范围为 1100μg/L,5 种多环芳烃的检出限(LOD)均低于 0.1μg/L,除苯并[k]荧蒽外其余 4 种多环芳烃的定量限(LOQ)均为 0.2μg/L,苯并[k]荧蒽的 LOD 和 LOQ 分别为 0.1μg/L 和 0.8μg/L。分别采用该方法对两个污水处理厂的污水样品进行了测定,所有化合物的回收率为 67.8%113.2%,相对标准偏差(RSD)为 2.5%10.3%。与已有的方法相比,该方法具有快速、溶剂用量少、仪器样品通量提高 25 倍的优点。

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