Oil fingerprinting analysis using commercial solid phase extraction (SPE) cartridge and gas chromatography-mass spectrometry (GC-MS).

Abstract

This study used solid phase extraction (SPE) cartridges for rapid cleanup and fractionation of oil samples in oil fingerprinting analysis. A series of commercially available florisil cartridges, normal phase SPE cartridges, and silica gel/cyanopropyl (SiO2/C3-CN) SPE cartridges was selected for the fractionation of oil into aliphatic and aromatic hydrocarbons. The florisil cartridges and normal phase SPE cartridges can clean up the oil samples but are unable to separate them into two fractions. The SiO2/C3-CN (1 g/0.5 g) SPE cartridge successfully separated oil samples into aliphatic and aromatic fractions by eluting with 4 mL of hexane and 4 mL of dichloromethylene (DCM)/hexane (3 : 1, v:v), respectively. No cross-elution was observed between aliphatic and aromatic fractions when oil loading mass was less than 40 mg on the SiO2/C3-CN SPE cartridge. The relative standard deviation (RSD) of five replicates of SPE-GC-MS analysis of 5 mg of reference oil is 2.8%, 1.2%, and 6.9% for total n-alkanes, polycyclic aromatic hydrocarbons (PAHs), and biomarkers, respectively. The recoveries of six spiked deuterated surrogates were all above 95%. This SPE-GC-MS method was used for the fingerprinting analysis of various crude oils, refined petroleum products, and environmental sediment samples. The characterized target hydrocarbons included n-alkanes, unsubstituted priority PAHs and alkylated homologues, and biomarker terpanes and steranes. The concentration profiles and diagnostic ratios of target compounds are both comparable to those obtained by the conventional silica gel column-GC-MS method.