A multi-dimensional high performance liquid chromatographic method for fingerprinting polycyclic aromatic hydrocarbons and their alkyl-homologs in the heavy gas oil fraction of Alaskan North Slope crude

被引:27
作者
Aravanabhavan, Gurusankar S.
Helferty, Anjali
Hodson, Peter V.
Brown, R. Stephen [1 ]
机构
[1] Queens Univ, Sch Environm Studies, Dept Chem, Kingston, ON, Canada
[2] Queens Univ, Sch Environm Studies, Dept Biol, Kingston, ON K7L 3N6, Canada
关键词
un-substituted and alkyl-substituted PAH analysis; HPLC; crude oil; DAD detection; GROUP-TYPE SEPARATION; CHEMICALLY-BONDED AMINOSILANE; DIODE-ARRAY DETECTION; PETROLEUM-PRODUCTS; HPLC; INDUCTION; PHASE; IDENTIFICATION; TOXICITY; SAMPLES;
D O I
10.1016/j.chroma.2007.04.045
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We report an offline multi-dimensional high performance liquid chromatography (HPLC) technique for the group separation and analysis of PAHs in a heavy gas oil fraction (boiling range 287-481 degrees C). Waxes present in the heavy gas oil fraction were precipitated using cold acetone at -20 degrees C. Recovery studies showed that the extract contained 93% (+/- 1%; n = 3) of the PAHs that were originally present while the wax residue contained only 6% (+/- 0.5%; n = 3). PAHs present in the extract were fractionated, based on number of rings, into five fractions using a semi-preparative silica column (normal-phase HPLC). These fractions were analyzed using reverse-phase HPLC (RP-HPLC) coupled to a diode array detector (DAD). The method separated alkyl and un-substituted PAHs on two reverse-phase columns in series using an acetonitrile/water mobile phase. UV spectra of the chromatographic peaks were used to differentiate among PAH groups. Further characterization of PAHs within a given group to determine the substituent alkyl carbon number used retention time matching with a suite of alkyl-PAH standards. Naphthalene, dibenzothiophene, phenanthrene and fluorene and their C1-C4 alkyl isomers were quantified. The concentrations of these compounds obtained using the current method were compared with that of a GC-MS analysis obtained from an independent oil chemistry laboratory. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:124 / 133
页数:10
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