Summary
A resonant ionization mass spectrometer has been developed as an analytical tool for the detection of trace elements, especially of plutonium and other radionuclides. The sample, deposited on a rhenium filament, is evaporated by electrical heating and the atoms of the element under investigation are selectively ionized by laser light delivered from three dye lasers pumped by a copper vapour laser. The resulting photoions are detected in a time-of-flight spectrometer with a channelplate detector. For plutonium a mass resolution of M/δM=1500 was obtained and an overall detection efficiency of 4×10−6 was determined for stepwise excitation and ionization via autoionizing states. With a laser light bandwidth of 3–5 GHz neighbouring isotopes could be suppressed by a factor of 20 due to isotope shifts in the excitation transitions. The isotope composition of synthetic samples was measured and good agreement was found with mass spectroscopic results. The influence of the hyperfine structure on the isotope ratios is discussed.
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Ames F, Becker A, Kluge H-J, Rimke H, Ruster W, Trautmann N (1988) Fresenius Z Anal Chem 331:133–135
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Ruster, W., Ames, F., Mang, M. et al. Determination of trace elements by resonant ionization mass spectrometry (RIMS). Z. Anal. Chem. 331, 182–185 (1988). https://doi.org/10.1007/BF01105163
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DOI: https://doi.org/10.1007/BF01105163