Journal
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY
Volume 24, Issue 4, Pages 385-390Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b819879a
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- Stiftung Innovation RheinlandPfalz
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An inductively coupled plasma isotope dilution mass spectrometric (ICP-IDMS) method with direct introduction of the isotope-diluted sample into the plasma by laser ablation was developed for accurate, sensitive, fast, and simultaneous determination of trace metals in different oil samples. Metallo-organic solutions of isotope spikes (V-50, Cr-53, Cu-65, Fe-57, Ni-62, Zn-68, Cd-113, Sn-117, and Pb-206) were prepared from corresponding aqueous stock solutions by using liquid-liquid extraction of complexed metal ions in isobutyl methyl ketone. The isotope-diluted sample was absorbed by a cellulose material, which was fixed in a special PTFE holder for ablation, using a laser system with high ablation rates. Under these conditions, no time-dependent spike/analyte fractionation was observed for the metalloorganic spike/oil mixtures and the measured isotope ratios of the isotope-diluted samples remained constant over the whole ablation time, which is a necessary precondition for accurate results with the isotope dilution technique. The accuracy of LA-ICP-IDMS determinations was demonstrated by analyzing the fuel oil reference material BCR 1634c, certified for vanadium and nickel, a commercially available oil based standard (SCP-21) for nine metals, and by comparing LA-ICP-IDMS results with those obtained by ICP-IDMS using microwave-assisted sample digestion. Detection limits in the range of 0.02 mu g g(-1) (V) to 0.2 mu g g(-1)(Fe) were obtained for LA-ICP-IDMS by total analysis times per sample of only 10 min. Three crude oil samples of different origin with vanadium, nickel, and iron concentrations in the range of 2-60 mu g g(-1) were also analyzed, indicating iron heterogeneities by the relatively high standard deviation.
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