Rapid determination of 16 polycyclic aromatic hydrocarbons in PM2.5 by microwave assisted extraction-high performance liquid chromatography

被引:14
作者
Yuan, Xiaoxue [1 ]
You, Fan [1 ]
Yong, Li [1 ]
Yang, Changxiao [1 ]
Zhu, Lan [1 ]
Hu, Bin [1 ]
Liu, Tao [1 ]
机构
[1] Sichuan Ctr Dis Control & Prevent, Inst Physicochem Detect, Key Lab Physicochem Detect Poisoning Sichuan Prov, 6 Zhongxue Rd, Chengdu 610041, Sichuan, Peoples R China
关键词
PM2.5; Polycyclic aromatic hydrocarbons; High performance liquid chromatography; Microwave assisted extraction; QUADRUPOLE MASS-SPECTROMETRY; PARTICULATE MATTER; SOLVENT-EXTRACTION; AIR; PHASE; SAMPLES; MICROEXTRACTION; PARTICLES; PAHS;
D O I
10.1016/j.microc.2018.09.029
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this article, a method using magnetic stirring and microwave assisted extraction-high performance liquid chromatography has been developed for rapid determination of 16 polycyclic aromatic hydrocarbons (PAHs) in fine particulate matter (PM2.5) in ambient air. PAHs in PM2.5 captured on glass fiber filters were directly extracted only using 4 mL acetonitrile in a microwave extractor with magnetic stirring. Compared with dozens of minutes reported previously, the extraction time of this work only needs 6 min. After filtered through a hydrophobic membrane, the extract was directly injected for analysis. It also greatly shortened the duration of sample preparation. The operating procedures have been simplified, avoiding loss of analytes and systematic errors resulting from solvent replacement, concentration and nitrogen blowing and thereby ensuring a stable extraction efficiency, accurate and reliable analysis. The 16 PAHs were well separated on a ZORBAX eclipse PAH column using acetonitrile and water as mobile phases and detected by an ultraviolet detector and a fluorescence detector in tandem. Good linearity was demonstrated over the concentration range of 0.025 mu g/mL to 5.000 mu g/mL, with correlation coefficients being not < 0.9998. The spiked recoveries were between 78.7% and 115.6%. The relative standard deviation ranged from 0.7% to 7.8%. The detection limits varied from 0.008 ng/m(3) to 0.075 ng/m(3). The method is rapid, environmentally friendly, accurate and sensitive with high extraction efficiency, convenient operation and strong resistance to interference. It is suitable for simultaneous determination of 16 PAHs in samples delivered in bulk.
引用
收藏
页码:391 / 396
页数:6
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