Kuosmanen K, Hyötyläinen T, Hartonen K, Jönsson J A, Riekkola M-L
Laboratory of Analytical Chemistry, Department of Chemistry, University of Helsinki, P.O. Box 55, Finland.
Anal Bioanal Chem. 2003 Feb;375(3):389-99. doi: 10.1007/s00216-002-1685-0. Epub 2003 Jan 4.
Pressurised hot water extraction (PHWE) was coupled on-line with microporous membrane liquid-liquid extraction (MMLLE) and gas chromatography (GC) in the analysis of polycyclic aromatic hydrocarbon (PAH) compounds in soil. The MMLLE serves as a trapping device after the PHWE. Water from PHWE is directed to the donor side of the membrane unit and the analytes are extracted to the acceptor solution on the other side of the membrane. The role of MMLLE is to clean and concentrate the extract, which is then transferred on-line to the GC via a sample loop and an on-column interface using partially concurrent solvent evaporation. Separate optimisation of MMLLE and simulations of the PHWE-MMLLE connection were carried out before the actual on-line coupling. After optimisation of the whole on-line system, the efficiencies of the PHWE-MMLLE-GC and PHWE-solid-phase trap extractions were compared. The PHWE-MMLLE-GC method allowed on-line analysis of soil samples. The method was linear, with limits of detection in the range 0.05-0.13 ng and limits of quantification 0.65-1.66 microg g(-1). Comparison of the results with those obtained by other techniques confirmed the good performance.
在土壤中多环芳烃(PAH)化合物分析中,将加压热水萃取(PHWE)与微孔膜液液萃取(MMLLE)和气相色谱(GC)在线联用。MMLLE在PHWE之后用作捕集装置。PHWE产生的水被导向膜单元的供体侧,分析物被萃取到膜另一侧的接受溶液中。MMLLE的作用是净化和浓缩萃取物,然后通过样品环和柱上进样接口,利用部分同时溶剂蒸发将其在线转移至GC。在实际在线联用之前,分别对MMLLE进行了优化,并对PHWE - MMLLE连接进行了模拟。在对整个在线系统进行优化之后,比较了PHWE - MMLLE - GC和PHWE - 固相捕集萃取的效率。PHWE - MMLLE - GC方法可对土壤样品进行在线分析。该方法呈线性,检测限在0.05 - 0.13 ng范围内,定量限为0.65 - 1.66 μg g⁻¹。将结果与其他技术所得结果进行比较,证实了该方法的良好性能。