Salaices Avila Manuel Alejandro, Breiter Roman, Mott Henry
Lehrstuhl für Umweltverfahrenstechnik und Recycling, Friedrich-Alexander-Universität Erlangen-Nürnberg, Paul-Gordan-Strasse 3, 91052 Erlangen, Germany.
Chemosphere. 2007 Jan;66(1):18-29. doi: 10.1016/j.chemosphere.2006.05.069. Epub 2006 Jul 17.
Solid-phase microextraction (SPME) with gas chromatography is to be used for assay of effluent liquid samples from soil column experiments associated with VOC fate/transport studies. One goal of the fate/transport studies is to develop accurate, highly reproducible column breakthrough curves for 1,2-cis-dichloroethylene (cis-DCE) and trichloroethylene (TCE) to better understand interactions with selected natural solid phases. For SPME, the influences of the sample equilibration time, extraction temperature and the ratio of volume of sample bottle to that of the liquid sample (V(T)/V(w)) are the critical factors that could influence accuracy and precision of the measured results. Equilibrium between the gas phase and liquid phase was attained after 200 min of equilibration time. The temperature must be carefully controlled due to variation of both the Henry's constant (K(h)) and the fibre/gas phase distribution coefficient (K(fg)). K(h) decreases with decreasing temperature while K(fg) increases. Low V(T)/V(w) yields better sensitivity but results in analyte losses and negative bias of the resultant assay. High V(T)/V(w) ratio yields reduced sensitivity but analyte losses were found to be minimal, leading to better accuracy and reproducibility. A fast SPME method was achieved, 5 min for SPME extraction and 3.10 min for GC analysis. A linear calibration function in the gas phase was developed to analyse the breakthrough curve data, linear between a range of 0.9-236 microgl(-1), and a detection limit lower than 5 microgl(-1).
固相微萃取(SPME)结合气相色谱法将用于分析与挥发性有机化合物(VOC)归宿/迁移研究相关的土壤柱实验流出液样品。归宿/迁移研究的一个目标是为1,2-顺式二氯乙烯(顺式-DCE)和三氯乙烯(TCE)绘制准确、高度可重复的柱突破曲线,以更好地理解与选定天然固相的相互作用。对于SPME,样品平衡时间、萃取温度以及样品瓶体积与液体样品体积之比(V(T)/V(w))是可能影响测量结果准确性和精密度的关键因素。平衡200分钟后,气相和液相达到平衡。由于亨利常数(K(h))和纤维/气相分配系数(K(fg))都会变化,因此必须仔细控制温度。K(h)随温度降低而减小,而K(fg)则随温度升高而增大。低V(T)/V(w)可产生更好的灵敏度,但会导致分析物损失和最终测定结果出现负偏差。高V(T)/V(w)比会降低灵敏度,但分析物损失最小,从而具有更好的准确性和可重复性。实现了一种快速SPME方法,SPME萃取需5分钟,GC分析需3.10分钟。开发了一种气相线性校准函数来分析突破曲线数据,在0.9 - 236微克/升范围内呈线性,检测限低于5微克/升。