Large-volume injection combined with gas chromatography/isotope ratio mass spectrometry for the analysis of polycyclic aromatic hydrocarbons

RATIONALE Compound‐specific stable isotope analyses of carbon require relatively large amounts of sample for reliable analyses. Commonly applied injections of 1 μL may thus be insufficient for samples with low concentrations of pollutants (e.g. air particulate matter) or when the amount of a sample...

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Published inRapid communications in mass spectrometry Vol. 28; no. 2; pp. 200 - 208
Main Authors Buczyńska, Anna J., Geypens, Benny, Van Grieken, Rene, De Wael, Karolien
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 30.01.2014
Wiley Subscription Services, Inc
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Summary:RATIONALE Compound‐specific stable isotope analyses of carbon require relatively large amounts of sample for reliable analyses. Commonly applied injections of 1 μL may thus be insufficient for samples with low concentrations of pollutants (e.g. air particulate matter) or when the amount of a sample is limited. METHODS A Large‐Volume Injection (LVI) method for carbon stable isotope ratio analysis of Polycyclic Aromatic Hydrocarbons (PAHs) was optimized in this study. Gas chromatography/combustion/isotope ratio mass spectrometry (GCCIRMS) and ion trap mass spectrometry (ITMS) were used for the determination of stable carbon isotope ratios and quantification of compounds, respectively. RESULTS The optimized method resulted in very good reproducibility, even for the most volatile PAH, naphthalene, when a small amount of higher boiling co‐solvent was used. No significant fractionation of isotope ratios could be seen and the recoveries of analytes were similar to or better than that of a splitless cold injection. CONCLUSIONS Injection of 100 μL, instead of the commonly used 1 μL, increases the detection limit for PAHs significantly and/or simplifies the sample preparation step. Using our optimized method, stable carbon isotope ratios can be reliably measured in samples with concentrations of PAHs down to 0.05–0.1 ng μL–1. Copyright © 2013 John Wiley & Sons, Ltd.
Bibliography:ark:/67375/WNG-LV01QMJW-S
ArticleID:RCM6769
istex:CD6596C7F5E2A8DE07058BD34F861A5ABE0677AE
Supporting Info Item
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0951-4198
1097-0231
DOI:10.1002/rcm.6769