Recovery of226Ra in analysis is determined using225Ra separated by anion exchange from229Th and233U. Radium is coprecipitated with barium, and purified by ion exchange.226Ra and217At (decay product of225Ra) are measured by α-spectrometry.228Ra is determined both by β-counting228Ac and225Ac separated from228Ra and225Ra, and by α-counting its daughters after the decay of225Ra. Sources for α-spectrometry are prepared by electrodeposition (molecular plating).
Authors:L. Tandon, E. Hastings, J. Banar, J. Barnes, D. Beddingfield, D. Decker, J. Dyke, D. Farr, J. FitzPatrick, D. Gallimore, S. Garner, R. Gritzo, T. Hahn, G. Havrilla, B. Johnson, K. Kuhn, S. LaMont, D. Langner, C. Lewis, V. Majidi, P. Martinez, R. McCabe, S. Mecklenburg, D. Mercer, S. Meyers, V. Montoya, B. Patterson, R. Pereyra, D. Porterfield, J. Poths, D. Rademacher, C. Ruggiero, D. Schwartz, M. Scott, K. Spencer, R. Steiner, R. Villarreal, H. Volz, L. Walker, A. Wong, and C. Worley
The goal of nuclear forensics is to establish an unambiguous link between illicitly trafficked nuclear material and its origin.
The Los Alamos National Laboratory (LANL) Nuclear Materials Signatures Program has implemented a graded “conduct of operations”
type analysis flow path approach for determining the key nuclear, chemical, and physical signatures needed to identify the
manufacturing process, intended use, and origin of interdicted nuclear material. This analysis flow path includes both destructive
and non-destructive characterization techniques and has been exercized against different nuclear materials from LANL’s special
nuclear materials archive. Results obtained from the case study will be presented to highlight analytical techniques that
offer the critical attribution information.