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MS: Fachverband Massenspektrometrie
MS 5: Poster
MS 5.8: Poster
Mittwoch, 4. März 2026, 17:00–19:00, Philo 1. OG
Isotope shift and hyperfine structure measurements in curium — •R. Hasse1,3,4, T. E. Albrecht2, S. Berndt1, M. Block1,3,4, Ch. E. Düllmann1,3,4, J. G. Ezold5, U. Köster6, A. T. Loria Basto1,4, Ch. Mokry1,4, K. Myhre5, S. Raeder3,4, D. Renisch1,4, J. Runke1,3, S. K. Schrell5, M. Stemmler1,7, and K. Wendt1 — 1JGU, Mainz, Germany — 2CSM, Golden, CO, United States — 3GSI, Darmstadt, Germany — 4HIM, Mainz, Germany — 5ORNL, Oak Ridge, TN, United States — 6ILL, Grenoble, France — 7LU, Hannover, Germany
Curium (Z=96) is a minor actinide that is produced in nuclear reactors and therefore present in spent nuclear fuel. We report on high resolution resonance ionization mass spectrometry at RISIKO employing a narrowband Ti:Sa laser on the isotopes 242−248,250Cm to determine isotope shifts and the hyperfine structures of the odd-A isotopes 243,245,247Cm. For these measurements two ground state transitions from 5f76d7s9D2o to the excited states 5f76d7s7p9D3 and 5f86d7s9D3 were used in two-step ionization schemes. The sample sizes ranged from 107 atoms of the isotope 250Cm to 1013 atoms of the more abundant isotopes 246,248Cm. In a King-plot analysis these results are analyzed to derive so far missing nuclear mean square charge radii differences of the isotopes 242,247,250Cm. Additional analysis of the hyperfine structure using the SATLAS package yields the hyperfine parameters A and B.
Keywords: Isotope shift; RIMS; Curium