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« Previous AbstractA detailed comparison of analysis processes for MCC-IMS data in disease classification-Automated methods can replace manual peak annotations    Next Abstract"Isotope fractionation ((2)H/(1)H, (13)C/(12)C, (37)Cl/(35)Cl) in trichloromethane and trichloroethene caused by partitioning between gas phase and water" »

Anal Chem


Title:Compound Specific Stable Chlorine Isotopic Analysis of Volatile Aliphatic Compounds Using Gas Chromatography Hyphenated with Multiple Collector Inductively Coupled Plasma Mass Spectrometry
Author(s):Horst A; Renpenning J; Richnow HH; Gehre M;
Address:"Department of Isotope Biogeochemistry, Helmholtz Centre for Environmental Research - UFZ , Permoserstr. 15, 04318 Leipzig, Germany"
Journal Title:Anal Chem
Year:2017
Volume:20170824
Issue:17
Page Number:9131 - 9138
DOI: 10.1021/acs.analchem.7b01875
ISSN/ISBN:1520-6882 (Electronic) 0003-2700 (Linking)
Abstract:"Stable chlorine isotope analysis is increasingly used to characterize sources, transformation pathways, and sinks of organic aliphatic compounds, many of them being priority pollutants in groundwater and the atmosphere. A wider use of chlorine isotopes in environmental studies is still inhibited by limitations of the different analytical techniques such as high sample needs, offline preparation, confinement to few compounds and mediocre precision, respectively. Here we present a method for the delta(37)Cl determination in volatile aliphatic compounds using gas chromatography coupled with multiple-collector inductively coupled plasma mass spectrometry (GC-MC-ICPMS), which overcomes these limitations. The method was evaluated by using a suite of five previously offline characterized in-house standards and eight chlorinated methanes, ethanes, and ethenes. Other than in previous approaches using ICP methods for chlorine isotopes, isobaric interference of the (36)ArH dimer with (37)Cl was minimized by employing dry plasma conditions. Samples containing 2-3 nmol Cl injected on-column were sufficient to achieve a precision (sigma) of 0.1 mUr (1 milliurey = 0.001 = 1 per thousand) or better. Long-term reproducibility and accuracy was always better than 0.3 mUr if organics were analyzed in compound mixtures. Standardization is carried out by using a two-point calibration approach. Drift, even though very small in this study, is corrected by referencing versus an internal standard. The presented method offers a direct, universal, and compound-specific procedure to measure the delta(37)Cl of a wide array of organic compounds overcoming limitations of previous techniques with the benefits of high sensitivity and accuracy comparable to the best existing approaches"
Keywords:
Notes:"PubMed-not-MEDLINEHorst, Axel Renpenning, Julian Richnow, Hans-Hermann Gehre, Matthias eng Research Support, Non-U.S. Gov't 2017/08/25 Anal Chem. 2017 Sep 5; 89(17):9131-9138. doi: 10.1021/acs.analchem.7b01875. Epub 2017 Aug 24"

 
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