New Carissa Oil Spill: Challenges to Oil Spill Source Identification

2001 ◽  
Vol 2001 (1) ◽  
pp. 97-107
Author(s):  
Gary Moffatf

ABSTRACT High resolution gas chromatography (GC) and gas chromatography in conjunction with mass spectrometry (GCMS) were used as fingerprinting techniques in this study to link oil spilled from the New Carissa to oil taken from oil impacted locations. Analyses included normal and isoprenoid alkanes, hopanes, and steranes, as well as a range of polynuclear aromatic hydrocarbons (PAHS). The oil spilled from the New Carissa was initially thought to be limited to bunker oils. Therefore, chromatograms of these samples and selected ion monitoring (SIM) chromatograms of the components and their combinations were compared, and obvious mismatches were rejected. Initial comparisons seemed simple; however, as with the spill response itself, factors that most often are insignificant began to affect the chemical analyses. Complications and technical challenges using conventional fingerprinting methods arose for several reasons. Likely reasons are (1) the spilled oil weathered on continued exposure to environmental conditions; (2) burning could cause changes to the chemical fingerprint; and (3) potential inhomogeneity of the spill because of multiple fuel sources in five fuel tanks at the bottom of the vessel. The PAH fingerprint had limited resistance to weathering. Therefore, the hopane fingerprint was selected for its resistance to weathering and potential screening power. Preburn and postburn New Carissa oil was characterized using principal component analysis (PCA) to determine if new and seemingly unrelated tarballs could be derived from the New Carissa spill. Response personnel will benefit from the lessons learned about potential complications of oil identification and subsequent determination of origin.

1989 ◽  
Vol 72 (2) ◽  
pp. 349-354 ◽  
Author(s):  
Lee Q Huang

Abstract A multiresidue method was developed for the simultaneous determination of low parts per billion (ppb) concentrations of the herbicides alachlor, metolachlor, atrazine, and simazine in water and soil using isotope dilution gas chromatography/mass spectrometry (GC/MS). Known amounts of 15N,13C-alachlor and 2H5-atrazine were added to each sample as internal standards. The samples were then prepared by a solid phase extraction with no further cleanup. A high resolution GC/low resolution MS system with data acquisition in selected ion monitoring mode was used to quantitate herbicides in the extract. The limit of detection was 0.05 ppb for water and 0.5 ppb for soil. Accuracy greater than 80% and precision better than 4% was demonstrated with spiked samples.


1991 ◽  
Vol 74 (6) ◽  
pp. 968-973
Author(s):  
Aziz Geahchan ◽  
I Le Gren ◽  
Paul Chambon ◽  
Renee Chambon

Abstract An improved method has been developed for quantitative determination of poiynuciear aromatic hydrocarbons (PAHs) in pharmacopoeial paraffin and medicinal white oil samples. This new method combines 2 liquid-liquid partition and adsorption chromatography procedures with a 2-step purification on Sephadex LH 20 and liquid chromatography with fluorometric determination. Selective elution of PAHs results in absence of background fluorescence. The minimum detectable level ranges from 0.2 ppt for benzofluoranthene isomers to 200 ppt for acenaphthene. Recoveries of PAHs added at 7 ppm varied from 92.1 to 111.4%. When a variety of medicinal white oil samples were analyzed by this improved method, 27 PAHs were identified, including 11 suspected carcinogens. Their identities were confirmed by capillary gas chromatography.


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