Author: Collon, P.
Paper Title Page
TUPP01 Quantitative Determination of 146Sm/147Sm Ratios by Accelerator Mass Spectrometry with an ECR Ion Source and Linear Acceleration for 146Sm Half-Life Measurement 43
 
  • N. Kinoshita
    UTTAC, Tsukuba, Ibaraki, Japan
  • P. Collon, Y. Kashiv, D. Robertson, C.J. Schmitt, X.D. Tang
    University of Notre Dame, Indiana, USA
  • C. Deibel
    MSU, East Lansing, Michigan, USA
  • C. Deibel, B. DiGiovine, J.P. Greene, D. Henderson, C.L. Jiang, S.T. Marley, R.C. Pardo, E. Rehm, R.H. Scott, R.C. Vondrasek
    ANL, Argonne, USA
  • T. Nakanishi, A. Yokoyama
    Kanazawa University, Kanazawa, Japan
  • M. Paul
    The Hebrew University of Jerusalem, The Racah Institute of Physics, Jerusalem, Israel
 
  Funding: Supported by U.S. DOE, Office of Nuclear Physics, contract No. DE-AC02-06CH11357, NSF JINA Grant Nr. PHY0822648 and Science Research Prog. of Japan Society for the Promotion of Science (20740161)
The alpha-decaying 146Sm nuclide is used for chronology of the Solar System and silicate mantle differentiation in planets. We performed a new determination of 146Sm half-life by measuring 146Sm/147Sm alpha activity and atom ratios in 147Sm activated via (g,n), (n,2n) and (p,2n) reactions and obtained a value (68 Myr), smaller than that adopted so far (103 Myr), with important geochemical implications*. The experiment required determination of 146Sm/147Sm ratios by high-energy (6 MeV/u) accelerator mass spectrometry to discriminate 146Sm from isobaric 146Nd contaminant. Activated Sm targets were dissolved, chemically purified and reconverted to metallic Sm. Sputter cathodes, made by pressing the Sm metal into high-purity Al holders, were used to feed the Argonne ECR ion source. 146Sm22+, 147Sm22+ ions were alternately injected and accelerated with the ATLAS linac by proper scaling of ion source and accelerator components. A tightly-fitted quartz cylindrical liner was inserted in the ECR plasma chamber to reduce contamination from the walls. 146Sm ions were eventually counted in a gas-filled magnet and 147Sm ions either measured as charge current or counted after proper attenuation.
* N. Kinoshita et al., Science 334, 1614 (2012)
 
 
FRXA03 Laser Ablation of Actinides into an Electron Cyclotron Resonance Ion Sources for Accelerator Mass Spectroscopy 190
 
  • T. Palchan, F.G. Kondev, S.A. Kondrashev, C. Nair, R.C. Pardo, R.H. Scott, R.C. Vondrasek
    ANL, Argonne, USA
  • W. Bauder, P. Collon
    University of Notre Dame, Indiana, USA
  • J.F. Berg, T. Maddock, G. Palmotti, M. Salvatores, G. Youinou
    INL, Idaho Falls, Idaho, USA
  • G. Imel
    ISU, Pocatello, Idaho, USA
  • M. Paul
    The Hebrew University of Jerusalem, The Racah Institute of Physics, Jerusalem, Israel
  • M. Salvatores
    CEA Cadarache, Saint Paul Lez Durance, France
 
  Funding: This work is supported by the U.S. Department of Energy, Office of Nuclear Physics, under contract No. DE-AC02-06CH11357.
A project using accelerator mass spectrometry (AMS) is underway at the ATLAS facility to measure the atom densities of transmutation products present in samples irradiated in the Advanced Test Reactor at INL. These atom densities will be used to infer effective actinide neutron capture cross-sections ranging from Thorium to Califorium isotopes in different neutron spectra relevant to advanced fuel cycles. This project will require the measurement of many samples with high precision and accuracy. The AMS technique at ATLAS is based on production of highly-charged positive ions in an ECRIS followed by injection into a linear accelerator. We use a picosecond laser to ablate the actinide material into the ion source. We expect that the laser ablation technique will have higher efficiency and lower chamber contamination than sputtering or oven evaporation thus reducing 'cross talk' between samples. The results of off-line ablation tests and first results of an accelerate beam generated by the laser coupled to the ECR will be discussed as well as the overall project schedule.
 
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