土壤样品中131I和134Cs锗探测器的效率定标及体积源级联求和修正的简化计算

M. Asai, Y. Kaneya, Tetsuya K. Sato, K. Tsukada, K. Ooe, N. Sato, A. Toyoshima
{"title":"土壤样品中131I和134Cs锗探测器的效率定标及体积源级联求和修正的简化计算","authors":"M. Asai, Y. Kaneya, Tetsuya K. Sato, K. Tsukada, K. Ooe, N. Sato, A. Toyoshima","doi":"10.14494/JNRS.12.5","DOIUrl":null,"url":null,"abstract":"The accident of the Fukushima Daiichi Nuclear Power Plant dispersed a huge amount of radionuclides in the natural environment, and part of them were deposited on the ground surface in the extensive region of east Japan. Assessments of the deposition densities of radionuclides and their geographical distributions provide important quantitative bases for estimations of radiation exposures of the residents, transfer of radionuclides into agricultural products, costs of decontaminations, etc. The Japanese government in collaboration with a few hundreds of researchers in universities and associations carried out detailed measurements of radionuclides deposited on soil over the whole area of Fukushima prefecture. Independent of this work, we carried out measurements of radionuclides in soil samples collected in the north and east area of Ibaraki prefecture and in the east area of Tochigi prefecture. The soil samples were collected on May 21–22 and June 22 in 2011, and γ rays originating from the β decay of I, Cs, and Cs were observed with Ge detectors, whose details are described in a separate paper. To measure radioactivities in soil with a Ge detector, we have to know γ-ray detection efficiencies of the Ge detector for soil samples. Typically soil samples have a large volume and density. Thus, to determine the efficiencies of Ge detectors, it is necessary to prepare the standard soil sample which contains a known amount of radionuclides and whose shape, density, and elemental contents are approximately the same as those of soil samples. At first, we used a standard soil sample distributed by IAEA to measure the efficiencies. This soil sample contains 4.0–60 Bq kg of Am, Cd, Cs, Cs, Mn, and Co. However, these radioactivity concentrations were too weak to determine the detector efficiencies precisely. Moreover, this standard source does not contain radionuclides which emit γ rays with energies at the range of 90–600 keV. This makes it difficult to determine the efficiency for the 364 keV γ ray of I. A mixed γ-ray standard source which resembles soil samples in shape, density, and elemental contents is commercially available. However, typically it does not contain I and Cs. The efficiency at 364 keV for I is extracted from the efficiency calibration curve determined by using γ rays of, e.g., Hg (279 keV), Cr (320 keV), Sn (392 keV), Sr (514 keV), and Cs (662 keV). However, these radionuclides except Cs are not always available because of their short half-lives. For Cs, even if the efficiency calibration curve is determined precisely, one has to take account of the influence of the cascade summing effect which reduces or increases observed γ-ray peak counts, especially when the sample is placed at a close source-to-detector distance. For point sources, correction factors for the cascade summing effect are easily calculated using total efficiencies and full-energy peak efficiencies of Ge detectors determined experimentally. For volume sources, however, the efficiencies are different at different parts of the source, which leads to different summing corrections at each part. This forces us to confront a difficulty in obtaining the total and full-energy peak efficiencies at any parts of the volume source. The correction factor for a certain γ ray depends only on the decay scheme of the nuclide and on the geometry of the source and the detector. Thus, if we can prepare the standard source which contains the same radionuclide and has the same geometry (shape, density, and elemental contents) as those of soil samples, we can determine the contents of radionuclides in soil samples only through a comparison of observed γ-ray peak counts between the standard source and a soil sample, because the cascade summing corrections for both the standard source and a soil sample are identical, and thus they are cancelled out. The aim of the present study is to determine γ-ray detection efficiencies of Ge detectors for I, Cs, and Cs in soil samples, and to evaluate the cascade summing corrections for I and Cs in soil samples which has a large volume and density. For this purpose, we make standard soil samples containing Cs, Cs, Hf, and Zr.","PeriodicalId":16569,"journal":{"name":"Journal of nuclear and radiochemical sciences","volume":"16 1","pages":"5-10"},"PeriodicalIF":0.0000,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Efficiency Calibration of Ge Detector for 131I and 134Cs in Soil Samples and a Simplified Calculation of Cascade Summing Corrections for Volume Source\",\"authors\":\"M. Asai, Y. Kaneya, Tetsuya K. Sato, K. Tsukada, K. Ooe, N. Sato, A. Toyoshima\",\"doi\":\"10.14494/JNRS.12.5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The accident of the Fukushima Daiichi Nuclear Power Plant dispersed a huge amount of radionuclides in the natural environment, and part of them were deposited on the ground surface in the extensive region of east Japan. Assessments of the deposition densities of radionuclides and their geographical distributions provide important quantitative bases for estimations of radiation exposures of the residents, transfer of radionuclides into agricultural products, costs of decontaminations, etc. The Japanese government in collaboration with a few hundreds of researchers in universities and associations carried out detailed measurements of radionuclides deposited on soil over the whole area of Fukushima prefecture. Independent of this work, we carried out measurements of radionuclides in soil samples collected in the north and east area of Ibaraki prefecture and in the east area of Tochigi prefecture. The soil samples were collected on May 21–22 and June 22 in 2011, and γ rays originating from the β decay of I, Cs, and Cs were observed with Ge detectors, whose details are described in a separate paper. To measure radioactivities in soil with a Ge detector, we have to know γ-ray detection efficiencies of the Ge detector for soil samples. Typically soil samples have a large volume and density. Thus, to determine the efficiencies of Ge detectors, it is necessary to prepare the standard soil sample which contains a known amount of radionuclides and whose shape, density, and elemental contents are approximately the same as those of soil samples. At first, we used a standard soil sample distributed by IAEA to measure the efficiencies. This soil sample contains 4.0–60 Bq kg of Am, Cd, Cs, Cs, Mn, and Co. However, these radioactivity concentrations were too weak to determine the detector efficiencies precisely. Moreover, this standard source does not contain radionuclides which emit γ rays with energies at the range of 90–600 keV. This makes it difficult to determine the efficiency for the 364 keV γ ray of I. A mixed γ-ray standard source which resembles soil samples in shape, density, and elemental contents is commercially available. However, typically it does not contain I and Cs. The efficiency at 364 keV for I is extracted from the efficiency calibration curve determined by using γ rays of, e.g., Hg (279 keV), Cr (320 keV), Sn (392 keV), Sr (514 keV), and Cs (662 keV). However, these radionuclides except Cs are not always available because of their short half-lives. For Cs, even if the efficiency calibration curve is determined precisely, one has to take account of the influence of the cascade summing effect which reduces or increases observed γ-ray peak counts, especially when the sample is placed at a close source-to-detector distance. For point sources, correction factors for the cascade summing effect are easily calculated using total efficiencies and full-energy peak efficiencies of Ge detectors determined experimentally. For volume sources, however, the efficiencies are different at different parts of the source, which leads to different summing corrections at each part. This forces us to confront a difficulty in obtaining the total and full-energy peak efficiencies at any parts of the volume source. The correction factor for a certain γ ray depends only on the decay scheme of the nuclide and on the geometry of the source and the detector. Thus, if we can prepare the standard source which contains the same radionuclide and has the same geometry (shape, density, and elemental contents) as those of soil samples, we can determine the contents of radionuclides in soil samples only through a comparison of observed γ-ray peak counts between the standard source and a soil sample, because the cascade summing corrections for both the standard source and a soil sample are identical, and thus they are cancelled out. The aim of the present study is to determine γ-ray detection efficiencies of Ge detectors for I, Cs, and Cs in soil samples, and to evaluate the cascade summing corrections for I and Cs in soil samples which has a large volume and density. For this purpose, we make standard soil samples containing Cs, Cs, Hf, and Zr.\",\"PeriodicalId\":16569,\"journal\":{\"name\":\"Journal of nuclear and radiochemical sciences\",\"volume\":\"16 1\",\"pages\":\"5-10\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of nuclear and radiochemical sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14494/JNRS.12.5\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of nuclear and radiochemical sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14494/JNRS.12.5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

摘要

福岛第一核电站事故使大量放射性核素在自然环境中扩散,部分放射性核素沉积在日本东部广大地区的地表。放射性核素的沉积密度及其地理分布的评估为估计居民的辐射照射、放射性核素向农产品的转移、去污成本等提供了重要的定量依据。日本政府与大学和协会的数百名研究人员合作,对整个福岛县土壤中沉积的放射性核素进行了详细测量。在这项工作之外,我们对茨城县北部和东部地区以及枥木县东部地区收集的土壤样本中的放射性核素进行了测量。土壤样品于2011年5月21日至22日和6月22日收集,用Ge探测器观察到I, Cs和Cs的β衰变产生的γ射线,其细节在另一篇论文中描述。为了用锗探测器测量土壤中的放射性,我们必须知道锗探测器对土壤样品的γ射线检测效率。典型的土壤样品具有较大的体积和密度。因此,为了确定锗探测器的效率,有必要准备含有已知数量的放射性核素的标准土壤样品,其形状、密度和元素含量与土壤样品大致相同。首先,我们使用国际原子能机构分发的标准土壤样本来测量效率。该土壤样品含有4.0-60 Bq kg的Am、Cd、Cs、Cs、Mn和Co。然而,这些放射性浓度太弱,无法精确确定探测器的效率。此外,该标准源不含放射能量在90-600 keV范围内的γ射线的放射性核素。这使得很难确定i的364 keV γ射线的效率。一种混合γ射线标准源在形状、密度和元素含量上与土壤样品相似。然而,它通常不包含I和c。利用汞(279 keV)、铬(320 keV)、锡(392 keV)、锶(514 keV)和铯(662 keV)等γ射线测定的效率校准曲线,提取了I在364 keV下的效率。然而,除了铯以外,这些放射性核素并不总是可用的,因为它们的半衰期很短。对于Cs,即使精确地确定了效率校准曲线,也必须考虑级联求和效应的影响,该效应会减少或增加观测到的γ射线峰计数,特别是当样品放置在源到探测器的近距离时。对于点源,利用实验确定的Ge探测器的总效率和全能量峰值效率,可以很容易地计算出级联求和效应的校正因子。然而,对于体积源,源的不同部分的效率是不同的,这导致每个部分的求和修正不同。这迫使我们面对一个困难,即在体积源的任何部分获得总能量和全能量峰值效率。某一γ射线的校正系数仅取决于核素的衰变方式和源和探测器的几何形状。因此,如果我们可以制备含有相同放射性核素的标准源,并且具有与土壤样品相同的几何形状(形状、密度和元素含量),我们可以通过比较标准源和土壤样品之间观察到的γ射线峰计数来确定土壤样品中放射性核素的含量,因为标准源和土壤样品的级联求和更正是相同的,因此它们被抵消了。本研究的目的是确定Ge探测器对土壤样品中I, Cs和Cs的γ射线检测效率,并评估具有大体积和密度的土壤样品中I和Cs的级联求和更正。为此,我们制作了含有Cs, Cs, Hf和Zr的标准土壤样品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Efficiency Calibration of Ge Detector for 131I and 134Cs in Soil Samples and a Simplified Calculation of Cascade Summing Corrections for Volume Source
The accident of the Fukushima Daiichi Nuclear Power Plant dispersed a huge amount of radionuclides in the natural environment, and part of them were deposited on the ground surface in the extensive region of east Japan. Assessments of the deposition densities of radionuclides and their geographical distributions provide important quantitative bases for estimations of radiation exposures of the residents, transfer of radionuclides into agricultural products, costs of decontaminations, etc. The Japanese government in collaboration with a few hundreds of researchers in universities and associations carried out detailed measurements of radionuclides deposited on soil over the whole area of Fukushima prefecture. Independent of this work, we carried out measurements of radionuclides in soil samples collected in the north and east area of Ibaraki prefecture and in the east area of Tochigi prefecture. The soil samples were collected on May 21–22 and June 22 in 2011, and γ rays originating from the β decay of I, Cs, and Cs were observed with Ge detectors, whose details are described in a separate paper. To measure radioactivities in soil with a Ge detector, we have to know γ-ray detection efficiencies of the Ge detector for soil samples. Typically soil samples have a large volume and density. Thus, to determine the efficiencies of Ge detectors, it is necessary to prepare the standard soil sample which contains a known amount of radionuclides and whose shape, density, and elemental contents are approximately the same as those of soil samples. At first, we used a standard soil sample distributed by IAEA to measure the efficiencies. This soil sample contains 4.0–60 Bq kg of Am, Cd, Cs, Cs, Mn, and Co. However, these radioactivity concentrations were too weak to determine the detector efficiencies precisely. Moreover, this standard source does not contain radionuclides which emit γ rays with energies at the range of 90–600 keV. This makes it difficult to determine the efficiency for the 364 keV γ ray of I. A mixed γ-ray standard source which resembles soil samples in shape, density, and elemental contents is commercially available. However, typically it does not contain I and Cs. The efficiency at 364 keV for I is extracted from the efficiency calibration curve determined by using γ rays of, e.g., Hg (279 keV), Cr (320 keV), Sn (392 keV), Sr (514 keV), and Cs (662 keV). However, these radionuclides except Cs are not always available because of their short half-lives. For Cs, even if the efficiency calibration curve is determined precisely, one has to take account of the influence of the cascade summing effect which reduces or increases observed γ-ray peak counts, especially when the sample is placed at a close source-to-detector distance. For point sources, correction factors for the cascade summing effect are easily calculated using total efficiencies and full-energy peak efficiencies of Ge detectors determined experimentally. For volume sources, however, the efficiencies are different at different parts of the source, which leads to different summing corrections at each part. This forces us to confront a difficulty in obtaining the total and full-energy peak efficiencies at any parts of the volume source. The correction factor for a certain γ ray depends only on the decay scheme of the nuclide and on the geometry of the source and the detector. Thus, if we can prepare the standard source which contains the same radionuclide and has the same geometry (shape, density, and elemental contents) as those of soil samples, we can determine the contents of radionuclides in soil samples only through a comparison of observed γ-ray peak counts between the standard source and a soil sample, because the cascade summing corrections for both the standard source and a soil sample are identical, and thus they are cancelled out. The aim of the present study is to determine γ-ray detection efficiencies of Ge detectors for I, Cs, and Cs in soil samples, and to evaluate the cascade summing corrections for I and Cs in soil samples which has a large volume and density. For this purpose, we make standard soil samples containing Cs, Cs, Hf, and Zr.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Uptake of 131I, 134Cs and 137Cs in tulip (Tulipa gesneriana L.) after the Fukushima Daiichi nuclear accident and their translocation from its above ground parts to the bulb Physical and adsorption characteristics of geopolymers prepared using 1–5 M NaOH solution for immobilization of radioactive wastes Isothermal gas chromatography study of Zr and Hf tetrachlorides using radiotracers of 88Zr and 175Hf Phase transformation of mixed lanthanide oxides in an aqueous solution Sorption and desorption of radioactive organic iodine by silver doped zeolite and zeolite X
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1