Abstract

Light petroleum biomarkers such as bicyclic sesquiterpanes and diamondoids are ubiquitous components of crude oils and ancient sediments, and are also widely found in intermediate petroleum distillates and many finished petroleum products. These compounds are relatively resistant to biodegradation and light-to-medium evaporation weathering, thus particularly useful in oil-source correlation and differentiation for those cases where the traditional tri- to pentacyclic biomarkers are absent. This work utilized sesquiterpanes and diamondoids for fingerprinting and identification of light oils spilled on water. The gas chromatography/flame ionization detection (GC/FID) analysis and distribution profiles of polycyclic aromatic hydrocarbon (PAHs) and conventional biomarkers suggest that the spilled oils are mixtures of mainly gasoline and light diesel type fuel. Since potential source oil candidates were not available, and a large part of the hydrocarbons in gasoline and diesel co-eluted in chromatographic analysis, it is a challenge to quantify the gasoline and diesel in spill samples. It has been known from previous studies that the bulk concentrations of C14 to C16 sesquiterpanes are in the range of approximately 6,000 to 9,000 μg/g for many light diesel fuels, while little or no sesquiterpanes were detected in gasoline, light kerosene and heavy-end lubricating oils. The target sesquiterpanes in the spilled oil samples were determined to be in quite high concentrations: approximately 4,000 μg/g oil. Therefore, it was estimated that these spilled oil samples consist of approximately half gasoline and half light diesel. To verify the estimation, spilled samples were simulated by mixing a fresh gasoline and a light diesel with a similar carbon range as the spilled oils. Results from comparison of GC/FID chromatograms of the spilled oils with the simulated spill samples are consistent with that obtained from sesquiterpane analysis.

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