Abstract
Physics experiments, environmental surveillance, and treaty verification techniques continue to require increased sensitivity for detecting and quantifying radionuclides of interest. This can be done by detecting a greater fraction of gamma emissions from a sample (higher detection efficiency) and reducing instrument backgrounds. A current effort for increased sensitivity in high resolution gamma spectroscopy will produce an intrinsic germanium (HPGe) array designed for high detection efficiency, ultra-low-background performance, and useful coincidence efficiencies. The system design is optimized to accommodate filter paper samples, e.g. samples collected by the Radionuclide Aerosol Sampler/Analyzer (RASA). The system will provide high sensitivity for weak collections on atmospheric filter samples, as well as offering the potential to gather additional information from more active filters using gamma cascade coincidence detection. The current effort is constructing an ultra-low-background HPGe crystal array consisting of two vacuum cryostats, each housing a hexagonal array of 7 crystals on the order of 70% relative efficiency per crystal. Traditional methods for constructing ultra-low-background detectors are used, including use of materials known to be low in radioactive contaminants, use of ultra pure reagents, clean room assembly, etc. The cryostat will be constructed mainly from copper electroformed into near-final geometry at PNNL. Details of the detector design, simulation of efficiency and coincidence performance, HPGe crystal testing, and progress on cryostat construction are presented.
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Acknowledgements
We would like to thank the DOE and the NEM program for sponsorship of this work; U. S. Department of Energy, Office of Nonproliferation and National Security, Office of Research and Development. Contract No. DE-AC06-76RLO 1830.
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Keillor, M.E., Aalseth, C.E., Day, A.R. et al. Design and construction of an ultra-low-background 14-crystal germanium array for high efficiency and coincidence measurements. J Radioanal Nucl Chem 282, 703–708 (2009). https://doi.org/10.1007/s10967-009-0248-7
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DOI: https://doi.org/10.1007/s10967-009-0248-7