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Production, isolation and characterization of radiochemically pure 163Ho samples for the ECHo-project

  • Holger Dorrer EMAIL logo , Katerina Chrysalidis , Thomas Day Goodacre , Christoph E. Düllmann , Klaus Eberhardt , Christian Enss , Loredana Gastaldo , Raphael Haas , Jonathan Harding , Clemens Hassel , Karl Johnston , Tom Kieck , Ulli Köster , Bruce Marsh , Christoph Mokry , Sebastian Rothe , Jörg Runke , Fabian Schneider , Thierry Stora , Andreas Türler and Klaus Wendt
From the journal Radiochimica Acta

Abstract

Several experiments on the study of the electron neutrino mass are based on high-statistics measurements of the energy spectrum following electron capture of the radionuclide 163Ho. They rely on the availability of large, radiochemically pure samples of 163Ho. Here, we describe the production, separation, characterization, and sample production within the Electron Capture in Holmium-163 (ECHo) project. 163Ho has been produced by thermal neutron activation of enriched, prepurified 162Er targets in the high flux reactor of the Institut Laue-Langevin, Grenoble, France, in irradiations lasting up to 54 days. Irradiated targets were chemically processed by means of extraction chromatography, which allowed separating the formed Ho from the 162Er target-material and from the main byproducts 170Tm and 171Tm, which are co-produced in GBq amounts. Decontamination factors of >500 for Er and of >105 for Tm and yields of 3.6·1016 and 1.2·1018 atoms of 163Ho were obtained, corresponding to a recovery yield of 95 % of Ho in the chemical separation. The Ho-fraction was characterized by means of γ-ray spectrometry, Inductively-Coupled-Plasma Mass Spectrometry (ICP-MS), Resonance Ionization Mass Spectrometry (RIMS) and Neutron Activation Analysis (NAA). In this process, the thermal neutron capture cross section of 163Ho was measured to σHo-163 to Ho-164m= (23±3) b and σHo-163 to Ho-164g= (156±9) b for the formation of the two isomers of 164Ho. Specific samples were produced for further purification by mass separation to isolate 163Ho from the Ho-isotope mixture, as needed for obtaining the energy spectrum within ECHo. The partial efficiency for this second separation step is (32±5) %.

Acknowledgements

This work was carried out in the framework of the DFG Research Unit FOR 2202 (ECHo) and we acknowledge financial support from the DFG under contracts DU 1334/1-1, EN 299/7-1, and GA 2219/2-1. H.D. acknowledges additional support by the Stufe 1 funding of the Johannes Gutenberg University Mainz. This project has received funding through the European Union’s Seventh Framework Programme for Research and Technological Development under Grant Agreements 262010 (ENSAR), 267194 (COFUND), and 289191 (LA3NET). The authors would like to thank Alexander Voegele for irradiating samples for the Ho and Er tracer at SINQ, Silvia Koechli and Anja Eichler for performing the ICP-OES measurements, Tobias Reich and Samer Amayri for performing the ICP-MS analytics as well as Ernst Schaub for technical assistance.

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Received: 2017-9-7
Accepted: 2018-1-17
Published Online: 2018-3-6
Published in Print: 2018-7-26

©2018 Walter de Gruyter GmbH, Berlin/Boston

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