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    Target Preparation for Continuous Flow Accelerator Mass Spectrometry

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    Author
    Schneider, Robert J.
    Hayes, J. M.
    Von Reden, K. F.
    McNichol, Ann P.
    Eglinton, T. I.
    Wills, J. S. C.
    Issue Date
    1998-01-01
    Keywords
    compression
    microwave spectroscopy
    gas chromatography
    lignin
    petroleum
    volume
    combustion
    ions
    gaseous phase
    graphitization
    graphite
    native elements
    accelerator mass spectroscopy
    mass spectroscopy
    spectroscopy
    organic compounds
    sample preparation
    methods
    C 14
    carbon
    isotopes
    radioactive isotopes
    carbon dioxide
    absolute age
    carbonates
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    Citation
    Schneider, R. J., Hayes, J. M., Von Reden, K. F., McNichol, A. P., Eglinton, T. J., & Wills, J. S. C. (1998). Target preparation for continuous flow accelerator mass spectrometry. Radiocarbon, 40(1), 95-102.
    Publisher
    Department of Geosciences, The University of Arizona
    Journal
    Radiocarbon
    Description
    From the 16th International Radiocarbon Conference held in Gronigen, Netherlands, June 16-20, 1997.
    URI
    http://hdl.handle.net/10150/653749
    DOI
    10.1017/S0033822200017938
    Additional Links
    http://radiocarbon.webhost.uits.arizona.edu/
    Abstract
    For very small samples, it is difficult to prepare graphitic targets that will yield a useful and steady sputtered ion beam. Working with materials separated by preparative capillary gas chromatography, we have succeeded with amounts as small as 20 micrograms C. This seems to be a practical limit, as it involves 1) multiple chromatographic runs with trapping of effluent fractions, 2) recovery and combustion of the fractions, 3) graphitization and 4) compression of the resultant graphite/ cobalt matrix into a good sputter target. Through such slow and intricate work, radiocarbon ages of lignin derivatives and hydrocarbons from coastal sediments have been determined. If this could be accomplished as an "online" measurement by flowing the analytes directly into a microwave gas ion source, with a carrier gas, then the number of processing steps could be minimized. Such a system would be useful not just for chromatographic effluents, but for any gaseous material, such as CO2 produced from carbonates. We describe tests using such an ion source.
    Type
    Proceedings
    text
    Language
    en
    ISSN
    0033-8222
    ae974a485f413a2113503eed53cd6c53
    10.1017/S0033822200017938
    Scopus Count
    Collections
    Radiocarbon, Volume 40, Number 1 (1998)

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