Rapid determination of trace polycyclic aromatic hydrocarbons in particulate matter using accelerated solvent extraction followed by ultra high performance liquid chromatography with fluorescence detection

被引:6
|
作者
Xu, Tianci [1 ,2 ]
机构
[1] Liaoning Prov Environm Monitoring & Expt Ctr, Shenyang 110161, Peoples R China
[2] Liaoning Prov Key Lab Environm Monitoring Technol, Shenyang, Peoples R China
关键词
Accelerated solvent extraction; Fluorescence detection; Liquid chromatography; Particulate matter; Polycyclic aromatic hydrocarbons; TANDEM MASS-SPECTROMETRY; SOLID-PHASE EXTRACTION; GAS-CHROMATOGRAPHY; SAMPLES; SOIL; PARTICLES; EXPOSURE; AEROSOL; SILICA; CELLS;
D O I
10.1002/jssc.201501232
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method has been developed for the trace analysis of polycyclic aromatic hydrocarbons, which are known as persistent organic pollutants and ubiquitous constituents of fine particulate matter that causes growing airborne pollution. The method, which was especially for samples of airborne particulate matter less than 2.5 mu m in diameter, utilized accelerated solvent extraction and ultra high performance liquid chromatography with fluorescence detector. Four principal parameters of accelerated solvent extraction were optimized to obtain maximum extraction efficiency. Using the established synergetic programs of gradient elution and fluorescence wavelength switching, a rapid separation was achieved in 6.56 min with good linearity for 15 polycyclic aromatic hydrocarbons (coefficient of determination above 0.999). The limits of detection ranged from 0.833 to 10.0 pg/m(3). The precision of the method expressed as inter-day relative standard deviation ranged from 0.2 to 1%, which was calculated from nine repetitive measurements of 8.00 mu g/L analytes. Average spiked recoveries ranged from 71.6 to 97.7%, with the exception of naphthalene. The rapid, sensitive, and accurate method can meet the pressing needs of health risk assessment and increasingly heavy daily tasks of air quality monitoring.
引用
收藏
页码:1892 / 1899
页数:8
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