Key Laboratory of Northwest Water Resource, Environment and Ecology, MOE, Xi'an University of Architecture and Technology, Xi'an 710055, China.
Water Sci Technol. 2011;64(2):477-84. doi: 10.2166/wst.2011.710.
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.
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。