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  • 标题:Internal dose assessment of 148 Gd using isotope ratios of gamma-emitting 146 Gd or 153 Gd in accidently released spallation target particles
  • 本地全文:下载
  • 作者:C. Rääf ; V. Barkauskas ; K. Eriksson Stenström
  • 期刊名称:Scientific Reports
  • 电子版ISSN:2045-2322
  • 出版年度:2020
  • 卷号:10
  • 期号:1
  • 页码:1-11
  • DOI:10.1038/s41598-020-77718-3
  • 出版社:Springer Nature
  • 摘要:The pure alpha emitter 148Gd may have a significant radiological impact in terms of internal dose to exposed humans in case of accidental releases from a spallation source using a tungsten target, such as the one to be used in the European Spallation Source (ESS). In this work we aim to present an approach to indirectly estimate the whole-body burden of 148Gd and the associated committed effective dose in exposed humans, by means of high-resolution gamma spectrometry of the gamma-emitting radiogadolinium isotopes 146Gd and 153Gd that are accompanied by 148Gd generated from the operation of the tungsten target. Theoretical minimum detectable whole-body activity (MDA) and associated internal doses from 148Gd are calculated using a combination of existing biokinetic models and recent computer simulation studies on the generated isotope ratios of 146Gd/148Gd and 153Gd/148Gd in the ESS target. Of the two gamma-emitting gadolinium isotopes, 146Gd is initially the most sensitive indicator of the presence of 148Gd if whole-body counting is performed within a month after the release, using the twin photo peaks of 146Gd centered at 115.4 keV (MDA < 1 Bq for ingested 148Gd, and < 25 Bq for inhaled 148Gd). The corresponding minimum detectable committed effective doses will be less than 1 µSv for ingested 148Gd, but substantially higher for inhaled 148Gd (up to 0.3 mSv), depending on operation time of the target prior to the release. However, a few months after an atmospheric release, 153Gd becomes a much more sensitive indicator of body burdens of 148Gd, with a minimum detectable committed effective doses ranging from 18 to 77 µSv for chronic ingestion and between 0.65 to 2.7 mSv for acute inhalation in connection to the release. The main issue with this indirect method for 148Gd internal dose estimation, is whether the primary photon peaks from 146 and 153Gd can be detected undisturbed. Preliminary simulations show that nuclides such as 182Ta may potentially create perturbations that could impair this evaluation method, and which impact needs to be further studied in future safety assessments of accidental target releases.
  • 其他摘要:Abstract The pure alpha emitter 148 Gd may have a significant radiological impact in terms of internal dose to exposed humans in case of accidental releases from a spallation source using a tungsten target, such as the one to be used in the European Spallation Source (ESS). In this work we aim to present an approach to indirectly estimate the whole-body burden of 148 Gd and the associated committed effective dose in exposed humans, by means of high-resolution gamma spectrometry of the gamma-emitting radiogadolinium isotopes  146 Gd and 153 Gd that are accompanied by 148 Gd generated from the operation of the tungsten target. Theoretical minimum detectable whole-body activity (MDA) and associated internal doses from 148 Gd are calculated using a combination of existing biokinetic models and recent computer simulation studies on the generated isotope ratios of 146 Gd/ 148 Gd and 153 Gd/ 148 Gd in the ESS target. Of the two gamma-emitting gadolinium isotopes, 146 Gd is initially the most sensitive indicator of the presence of 148 Gd if whole-body counting is performed within a month after the release, using the twin photo peaks of 146 Gd centered at 115.4 keV (MDA < 1 Bq for ingested 148 Gd, and < 25 Bq for inhaled 148 Gd). The corresponding minimum detectable committed effective doses will be less than 1 µSv for ingested 148 Gd, but substantially higher for inhaled 148 Gd (up to 0.3 mSv), depending on operation time of the target prior to the release. However, a few months after an atmospheric release, 153 Gd becomes a much more sensitive indicator of body burdens of 148 Gd, with a minimum detectable committed effective doses ranging from 18 to 77 µSv for chronic ingestion and between 0.65 to 2.7 mSv for acute inhalation in connection to the release. The main issue with this indirect method for 148 Gd internal dose estimation, is whether the primary photon peaks from 146 and 153 Gd can be detected undisturbed. Preliminary simulations show that nuclides such as 182 Ta may potentially create perturbations that could impair this evaluation method, and which impact needs to be further studied in future safety assessments of accidental target releases.
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