<p>The rapid identification of <InlineEquation ID="IEq4"> <EquationSource Format="TEX">\(\gamma\)</EquationSource> <EquationSource Format="MATHML"><math> <mi>γ</mi> </math></EquationSource> </InlineEquation>-emitting radionuclides with low activity levels in public areas is crucial for nuclear safety. However, classical methods rely on full-energy peaks in the integral spectrum, requiring sufficient count accumulation for evaluation, thereby limiting response time. The sequential Bayesian approach, which utilizes prior information and considers both photon energies and interarrival times, can significantly enhance the performance of radionuclides identification. This study proposes a theoretical optimization method for the traditional sequential Bayesian approach. Each photon is processed sequentially, and the corresponding posterior probability is updated in real time using a noninformative prior from the Bayesian theory. By comparing the posterior probabilities of the background and radionuclides based on the energy variance and time interval, the type of <InlineEquation ID="IEq5"> <EquationSource Format="TEX">\(\gamma\)</EquationSource> <EquationSource Format="MATHML"><math> <mi>γ</mi> </math></EquationSource> </InlineEquation>-rays can be identified (background characteristic <InlineEquation ID="IEq6"> <EquationSource Format="TEX">\(\gamma\)</EquationSource> <EquationSource Format="MATHML"><math> <mi>γ</mi> </math></EquationSource> </InlineEquation>-rays, Compton plateaus <InlineEquation ID="IEq7"> <EquationSource Format="TEX">\(\gamma\)</EquationSource> <EquationSource Format="MATHML"><math> <mi>γ</mi> </math></EquationSource> </InlineEquation>-rays, or radionuclide-specific characteristic <InlineEquation ID="IEq8"> <EquationSource Format="TEX">\(\gamma\)</EquationSource> <EquationSource Format="MATHML"><math> <mi>γ</mi> </math></EquationSource> </InlineEquation>-rays). By integrating the information from these multiple characteristic <InlineEquation ID="IEq9"> <EquationSource Format="TEX">\(\gamma\)</EquationSource> <EquationSource Format="MATHML"><math> <mi>γ</mi> </math></EquationSource> </InlineEquation>-rays, the presence and type of radionuclides were determined based on the final decision function and a set threshold. Based on theoretical research, verification experiments were conducted using a <InlineEquation ID="IEq10"> <EquationSource Format="TEX">\(\hbox {LaBr}_3\)</EquationSource> <EquationSource Format="MATHML"><math> <msub> <mtext>LaBr</mtext> <mn>3</mn> </msub> </math></EquationSource> </InlineEquation>(Ce) detector in both low-and natural background radiation environments with typical radionuclides (<sup>137</sup>Cs, <sup>60</sup>Co, and <sup>133</sup>Ba). The results show that this approach can identify <sup>137</sup>Cs in 7.9 s and 8.5 s (source dose rate contribution: approximately <InlineEquation ID="IEq11"> <EquationSource Format="TEX">\(6.5\times 10^{-3}\)</EquationSource> <EquationSource Format="MATHML"><math> <mrow> <mn>6.5</mn> <mo>×</mo> <msup> <mn>10</mn> <mrow> <mo>-</mo> <mn>3</mn> </mrow> </msup> </mrow> </math></EquationSource> </InlineEquation> μGy/h), <sup>60</sup>Co in 8.1 s and 9.8 s (approximately <InlineEquation ID="IEq13"> <EquationSource Format="TEX">\(4.8\times 10^{-2}\)</EquationSource> <EquationSource Format="MATHML"><math> <mrow> <mn>4.8</mn> <mo>×</mo> <msup> <mn>10</mn> <mrow> <mo>-</mo> <mn>2</mn> </mrow> </msup> </mrow> </math></EquationSource> </InlineEquation> μGy/h), and <sup>133</sup>Ba in 4.05 s and 5.99 s (approximately <InlineEquation ID="IEq15"> <EquationSource Format="TEX">\(3.4\times 10^{-2}\)</EquationSource> <EquationSource Format="MATHML"><math> <mrow> <mn>3.4</mn> <mo>×</mo> <msup> <mn>10</mn> <mrow> <mo>-</mo> <mn>2</mn> </mrow> </msup> </mrow> </math></EquationSource> </InlineEquation> μGy/h) under low and natural background radiation, respectively, with a miss rate below <InlineEquation ID="IEq17"> <EquationSource Format="TEX">\(0.01 \%\)</EquationSource> <EquationSource Format="MATHML"><math> <mrow> <mn>0.01</mn> <mo>%</mo> </mrow> </math></EquationSource> </InlineEquation>. This demonstrates the effectiveness of the proposed approach for fast radionuclides identification, even at low activity levels and highlights its potential for enhancing public safety in diverse radiation environments.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Fast identification of \(\gamma\)-emitting radionuclides based on sequential Bayesian approach

  • Xuan Zhang,
  • Jian-Wei Huang,
  • Lin-Jian Wan,
  • Jia-Cheng Liu,
  • Xiao-Le Zhang,
  • De-Hong Li,
  • Fei Tuo,
  • Zhi-Jun Yang

摘要

The rapid identification of \(\gamma\) γ -emitting radionuclides with low activity levels in public areas is crucial for nuclear safety. However, classical methods rely on full-energy peaks in the integral spectrum, requiring sufficient count accumulation for evaluation, thereby limiting response time. The sequential Bayesian approach, which utilizes prior information and considers both photon energies and interarrival times, can significantly enhance the performance of radionuclides identification. This study proposes a theoretical optimization method for the traditional sequential Bayesian approach. Each photon is processed sequentially, and the corresponding posterior probability is updated in real time using a noninformative prior from the Bayesian theory. By comparing the posterior probabilities of the background and radionuclides based on the energy variance and time interval, the type of \(\gamma\) γ -rays can be identified (background characteristic \(\gamma\) γ -rays, Compton plateaus \(\gamma\) γ -rays, or radionuclide-specific characteristic \(\gamma\) γ -rays). By integrating the information from these multiple characteristic \(\gamma\) γ -rays, the presence and type of radionuclides were determined based on the final decision function and a set threshold. Based on theoretical research, verification experiments were conducted using a \(\hbox {LaBr}_3\) LaBr 3 (Ce) detector in both low-and natural background radiation environments with typical radionuclides (137Cs, 60Co, and 133Ba). The results show that this approach can identify 137Cs in 7.9 s and 8.5 s (source dose rate contribution: approximately \(6.5\times 10^{-3}\) 6.5 × 10 - 3 μGy/h), 60Co in 8.1 s and 9.8 s (approximately \(4.8\times 10^{-2}\) 4.8 × 10 - 2 μGy/h), and 133Ba in 4.05 s and 5.99 s (approximately \(3.4\times 10^{-2}\) 3.4 × 10 - 2 μGy/h) under low and natural background radiation, respectively, with a miss rate below \(0.01 \%\) 0.01 % . This demonstrates the effectiveness of the proposed approach for fast radionuclides identification, even at low activity levels and highlights its potential for enhancing public safety in diverse radiation environments.