Target Preparation for Continuous Flow Accelerator Mass Spectrometry
AuthorSchneider, Robert J.
Hayes, J. M.
Von Reden, K. F.
McNichol, Ann P.
Eglinton, T. I.
Wills, J. S. C.
accelerator mass spectroscopy
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CitationSchneider, 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.
DescriptionFrom the 16th International Radiocarbon Conference held in Gronigen, Netherlands, June 16-20, 1997.
AbstractFor 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.