Mao Debin, Van De Weghe Hendrik, Diels Ludo, De Brucker Nicole, Lookman Richard, Vanermen Guido
Flemish Institute for Technological Research (VITO), Boeretang 200, Mol, Belgium.
J Chromatogr A. 2008 Jan 25;1179(1):33-40. doi: 10.1016/j.chroma.2007.09.085. Epub 2007 Oct 11.
Successful remediation of oil-contaminated soils relies on a sound preceding characterization of the oil chemical composition and physicochemical properties. Comprehensive two-dimensional gas chromatography with flame ionization detection (GCxGC/FID) is known to be very suitable for the analysis of complex samples such as petroleum hydrocarbons. However, in spite of the high-separation power offered by GCxGC, it fails to completely separate certain hydrocarbon groups in petroleum hydrocarbon mixtures. This hampers a detailed chemical composition assessment which can lead to wrong conclusions on the behaviour of the oil in soil systems, e.g. biological degradability and water solubility. This paper describes a high-performance liquid chromatography (HPLC) system with a silver-modified column as a prefractionation step to GCxGC to improve chemical identification. With HPLC, the petroleum hydrocarbons were baseline separated into a saturated fraction (including alkanes and cycloalkanes) and an unsaturated fraction (including alkenes, aromatic hydrocarbons and heterocyclic components). Each fraction eluted in a small time window limiting the dilution caused by HPLC. The two fractions were collected and quantitatively analyzed with GCxGC/FID. Cold splitless injection of 4 microl was adopted to compensate the dilution caused by the prefractionation step. With oil-spiked soil samples, a good reproducibility was obtained (RSD=3.5%; n=7) and the recovery was satisfactory (87.7%).
成功修复受油污染的土壤依赖于对油的化学成分和物理化学性质进行合理的前期表征。带有火焰离子化检测的全二维气相色谱法(GCxGC/FID)已知非常适合分析诸如石油烃之类的复杂样品。然而,尽管GCxGC具有高分离能力,但它无法完全分离石油烃混合物中的某些烃类基团。这妨碍了详细的化学成分评估,可能导致对油在土壤系统中的行为得出错误结论,例如生物降解性和水溶性。本文描述了一种配备银改性柱的高效液相色谱(HPLC)系统,作为GCxGC的预分离步骤以改善化学鉴定。通过HPLC,石油烃被基线分离为饱和馏分(包括烷烃和环烷烃)和不饱和馏分(包括烯烃、芳烃和杂环成分)。每个馏分在一个小的时间窗口内洗脱,限制了由HPLC引起的稀释。收集这两个馏分并用GCxGC/FID进行定量分析。采用4微升的冷不分流进样来补偿预分离步骤引起的稀释。对于加标油的土壤样品,获得了良好的重现性(RSD = 3.5%;n = 7),回收率也令人满意(87.7%)。