Lundstedt Staffan, Haglund Peter, Oberg Lars
Environmental Chemistry, Department of Chemistry, Umeå University, SE-901 87 Umeå, Sweden.
Anal Chem. 2006 May 1;78(9):2993-3000. doi: 10.1021/ac052178f.
In this study, a selective pressurized liquid extraction (PLE) method which can extract polycyclic aromatic hydrocarbons (PAHs) and their oxygenated derivatives (oxy-PAHs) from contaminated soil and simultaneously separate them into two fractions was developed. The method uses extraction cells packed with a chromatographic adsorbent and extraction solvents of increasing polarity. Several experiments were conducted on both spiked and authentic contaminated soil samples. Different types of adsorbents, combinations of extraction solvents, and extraction temperatures were tested in order to find a method that could fulfill the purpose of the study. The final method was based on extraction cells packed with 2% deactivated silica gel. The PAHs were extracted with cyclohexane/dichloromethane (9:1) at 120 degrees C, after which the oxy-PAHs where extracted with cyclohexane/dichloromethane (1:3) at 150 degrees C. The PAHs and oxy-PAHs were efficiently separated into two fractions, and only trace amounts of some compounds were found in the inappropriate fraction. The recoveries of the PAHs were mostly above 70% and of the oxy-PAHs, above 90%. The linearity of the method was good, and the calibration curves for most compounds had a regression coefficient better than 0.99 and an intercept close to the origin of coordinates. When the selective PLE method was applied to seven authentic soil samples, the results were found to be in good agreement with those of a reference method based on Soxhlet extraction and silica gel cleanup and also in good agreement with the certified reference values available for one of the soils. The selective PLE method is faster and consumes less solvent than a traditional method based on separate extraction and fractionation steps. The selective PLE method is, therefore, suitable for the concurrent analysis of PAHs and oxy-PAHs during large-scale soil contamination studies. This will provide more information about the soil contamination and the levels of toxicity than an ordinary PAH analysis.
在本研究中,开发了一种选择性加压液体萃取(PLE)方法,该方法可从污染土壤中萃取多环芳烃(PAHs)及其氧化衍生物(含氧PAHs),并同时将它们分离为两个馏分。该方法使用填充有色谱吸附剂的萃取池和极性递增的萃取溶剂。对加标和真实污染土壤样品都进行了几项实验。测试了不同类型的吸附剂、萃取溶剂组合和萃取温度,以找到一种能够实现本研究目的的方法。最终方法基于填充2%失活硅胶的萃取池。PAHs在120℃下用环己烷/二氯甲烷(9:1)萃取,之后含氧PAHs在150℃下用环己烷/二氯甲烷(1:3)萃取。PAHs和含氧PAHs被有效地分离为两个馏分,在不合适的馏分中仅发现痕量的某些化合物。PAHs的回收率大多高于70%,含氧PAHs的回收率高于90%。该方法的线性良好,大多数化合物的校准曲线回归系数优于0.99,截距接近坐标原点。当将选择性PLE方法应用于七个真实土壤样品时,发现结果与基于索氏萃取和硅胶净化的参考方法的结果高度一致,并且与其中一种土壤的认证参考值也高度一致。与基于单独萃取和分馏步骤的传统方法相比,选择性PLE方法更快且消耗的溶剂更少。因此,选择性PLE方法适用于大规模土壤污染研究期间PAHs和含氧PAHs的同时分析。这将比普通的PAH分析提供更多关于土壤污染和毒性水平的信息。