Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1204981 | Journal of Chromatography A | 2008 | 6 Pages |
A modified headspace liquid-phase microextraction (HS-LPME) method was studied for the extraction of chlorophenols (CPs) from aqueous samples with complicated matrices, before gas chromatographic (GC) analysis with electron capture detection (ECD). Microwave heating was applied to accelerate the evaporation of CPs into the headspace, and an external-cooling system was used to control the sampling temperature. Conditions influencing extraction efficiency, such as the LPME-solvent, the sampling position of LPME, the sampling temperature, microwave power, and irradiation time (the same as sampling time), sample pH, and salt addition were thoroughly optimized. Experimental results indicated that the extraction of CPs from a 10 mL aquatic sample (pH 1.0) was achieved with the best efficiency through the use of 1-octanol as solvent, microwave irradiation of 167 W, and sampling at 45 °C for 10 min. The detections were linear in the concentration of 5.0–100 μg/L for 2,4-dichlorophenol (2,4-DCP), and 0.5–10 μg/L for 2,4,6-trichlorophenol (2,4,6-TCP), 2,3,4,6-tetrachlorophenol (2,3,4,6-TeCP) and pentachlorophenol (PCP). Detection limits were found to be 0.7, 0.04, 0.07, and 0.08 μg/L for 2,4-DCP, 2,4,6-TCP, 2,3,4,6-TeCP, and PCP, respectively. A landfill leachate sample was analyzed with recovery between 83 and 102%. The present method was proven to serve as a simple, sensitive, and rapid procedure for CP analysis in an aqueous sample.