中文摘要：

建立了连续流动-固相微萃取富集、气相色谱测定水中多环芳烃的方法，探讨了流量和溶液体积对萃取效果的影响。方法在0μg／L-40μg／L范围内线性良好，8种多环芳烃的检出限为0．05μg／L-0．5μg／L，样品测定的相对标准偏差〈7％，加标回收率为87．0％～112％。

英文摘要：

The method was established for polycyclic aromatic hydrocarbons determination by continuous aqueous sample flow-solid phase micro extraction/gas chromatography. The flow and solution volume on the effects of extraction were discussed. The good linear in the range from 0 μg/L to 40 μg/L, the detection limits of 8 kinds of polycyclic aromatic hydrocarbons from 0.05 μg/L to 0.5 μg/L, the relative standard deviation of samples 〈7% , the recoveries from 87.0% to 112%.