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Near-infrared scintillation properties of Nd-doped CaYAl3O7 single crystals 掺钕 CaYAl3O7 单晶体的近红外闪烁特性。
IF 1.6 3区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR Pub Date : 2024-10-22 DOI: 10.1016/j.apradiso.2024.111559
Akihiro Nishikawa, Kensei Ichiba, Takumi Kato, Daisuke Nakauchi, Noriaki Kawaguchi, Takayuki Yanagida
We prepared Nd-doped CaYAl3O7 single crystals with different Nd concentrations of 0.1, 0.5, 1.0, 5.0, 10, and 20% by the floating zone method. Photoluminescence (PL) and scintillation properties of all the samples were investigated, and the performance as near-infrared (NIR) scintillators was evaluated. All the samples exhibited some luminescence peaks of 4f-4f transitions of Nd3+ in PL and scintillation spectra at around 890, 1060, and 1300 nm. The 5.0% Nd-doped sample showed the highest PL quantum yield of 49.5%. In addition, the 5.0% Nd-doped sample had the highest scintillation intensity under X-ray irradiation among the samples, and the lowest detectable dose rate was 0.001 Gy/h.
我们采用浮区法制备了不同掺钕浓度(0.1、0.5、1.0、5.0、10 和 20%)的 CaYAl3O7 单晶。研究了所有样品的光致发光(PL)和闪烁特性,并评估了其作为近红外(NIR)闪烁体的性能。所有样品都在 890、1060 和 1300 nm 波长左右的光致发光和闪烁光谱中显示出一些 Nd3+ 的 4f-4f 转变发光峰。掺杂 5.0% Nd 的样品的 PL 量子产率最高,达到 49.5%。此外,掺杂 5.0% Nd 的样品在 X 射线辐照下的闪烁强度是所有样品中最高的,可检测到的最低剂量率为 0.001 Gy/h。
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引用次数: 0
Estimating Uncertainty in Actinide Intake Due to Unknown Time of Exposure 估算因暴露时间未知而导致的锕系元素摄入量的不确定性。
IF 1.6 3区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR Pub Date : 2024-10-19 DOI: 10.1016/j.apradiso.2024.111558
Minal Y. Nadar, S. Halder, L. Mishra, D.K. Akar, I.S. Singh, P.D. Sawant, P. Chaudhury
Bioassay of radiation workers handling actinides in powder form is carried out annually under routine monitoring program. In case of routine monitoring, as the day of intake is unknown, it is assumed that intake has occurred at the midpoint of monitoring interval. However, an uncertainty is introduced in intake estimation due to this assumption. In the present work, uncertainties were evaluated due to unknown time of intake of Type M and S compounds of Pu and U for annual and biennial monitoring interval. Lung and excreta monitoring methods were considered for uncertainty estimation along with the spread of ±1 month or ±2 months in measurements, at the end of monitoring interval. Annual lung monitoring is found to be the most robust and accurate method for assessment of intake of Type S compounds of Pu, Am and U when time of intake is unknown and Pu is detected using 241Am as a tracer. For Type M compounds, uncertainty was found to be higher than 3 for biennial monitoring interval. Uncertainty is found to be less than 3 for Type S compounds of Pu and U and also for Type M compounds of Pu for both, annual and biennial monitoring intervals using urine analysis. It is higher than 3 for Type M compounds of U for both the monitoring intervals. It is greater than 3 for both Type M and S compounds of Pu and U for both the monitoring intervals using fecal analysis.
在例行监测计划下,每年都会对处理粉末状锕系元素的辐射工作人员进行生物测定。在例行监测中,由于摄入日不详,因此假定摄入发生在监测间隔的中点。然而,由于这一假设,在摄入量估算中引入了不确定性。在本研究中,由于每年和每两年监测一次钚和铀的 M 型和 S 型化合物的未知摄入时间,对不确定性进行了评估。在估算不确定性时,考虑了肺和排泄物监测方法以及监测间隔结束时测量值的±1 个月或 ±2 个月的差值。当摄入时间未知,并使用 241Am 作为示踪剂检测钚时,发现年度肺监测是评估钚、镅和铀的 S 类化合物摄入量的最可靠、最准确的方法。就 M 类化合物而言,两年监测一次的不确定性大于 3。对于钚和铀的 S 类化合物以及钚的 M 类化合物,在使用尿液分析进行年度和双年度监测时,不确定性均小于 3。在两个监测周期内,M 类 U 化合物的不确定性均大于 3。利用粪便分析法,在两个监测周期内,钚和铀的 M 型和 S 型化合物的含量均大于 3。
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引用次数: 0
Validation of chromatographic methods, TLC and HPLC, to quantify known radiochemical impurities and the radiochemical purity the radiopharmaceutical [177Lu]Lu-PSMA I&T 验证色谱法(TLC 和 HPLC),以量化已知放射性化学杂质和放射性药物[177Lu]Lu-PSMA I&T 的放射性化学纯度
IF 1.6 3区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR Pub Date : 2024-10-18 DOI: 10.1016/j.apradiso.2024.111557
Joel M. Santos , Luiza M. Balieiro , Rodrigo S. Santos , Margareth M.N. Matsuda , Elaine B. Araújo
The Energy and Nuclear Research Institute (IPEN) is studying the production of the radiopharmaceutical [177Lu]Lu-PSMA I&T, in accordance with the good manufacturing practices recommended by the National Health Surveillance Agency (ANVISA), to be used in the therapy of prostate cancer. This work aims to validate chromatographic methods, Thin-Layer Chromatographic (TLC) and high-performance liquid chromatography (HPLC), to determine the radiochemical purity (RCP) of the product. The entire validation process of this work was based on ANVISA's RDC 166, 2017 and the Guide 10, version 1, 2017, guided the statistical treatments adopted. With the selectivity study we can observe that the presence of impurities or excess excipients in the sample does not interfere with the quantification of the product. The proposed methods were linear with linear correlation coefficients (r) above 0.99. The precision and repeatability presented relative standard deviation values lower than specified (RSD <5 %). The small controlled variations in the method suggested for the robustness test also did not affect the radiochemical purity of the product. In view of the results and in accordance with the criteria established by the National Health Surveillance Agency (ANVISA), the two chromatographic methods were validated in accordance with RDC 166, 2017, proving to be selective, precise, linear and robust. The validation of TLC and HPLC methods enables their application in the batch release routine of the new radiopharmaceutical at Radiopharmacy Center of IPEN.
能源与核研究所(IPEN)正在研究按照国家卫生监督局(ANVISA)建议的良好生产规范生产放射性药物[177Lu]Lu-PSMA I&T,用于治疗前列腺癌。这项工作旨在验证薄层色谱 (TLC) 和高效液相色谱 (HPLC) 等色谱方法,以确定产品的放射化学纯度 (RCP)。这项工作的整个验证过程以 ANVISA 的 RDC 166(2017 年)和《指南 10》(2017 年第 1 版)为基础,指导所采用的统计处理方法。通过选择性研究,我们可以发现样品中的杂质或过量辅料不会干扰产品的定量。所建议的方法具有线性关系,线性相关系数(r)高于 0.99。精确度和重复性的相对标准偏差值低于规定值(RSD <5%)。为进行稳健性测试而建议的方法中的微小可控变化也没有影响产品的放射化学纯度。鉴于上述结果,并根据国家卫生监督局(ANVISA)制定的标准,按照 RDC 166(2017 年)对两种色谱方法进行了验证,证明它们具有选择性、精确性、线性和稳健性。TLC 和 HPLC 方法的验证使其能够应用于 IPEN 放射药中心新放射性药物的批量放行程序。
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引用次数: 0
Investigation on preparation and properties of gel type 188W/188Re generator 凝胶型 188W/188Re 发生器的制备和性能研究。
IF 1.6 3区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR Pub Date : 2024-10-18 DOI: 10.1016/j.apradiso.2024.111553
Yanxia Cheng , Bo Li , Yingjiang Hu , Zuobiao Liu , Ning Luo , Yunming Chen , Jingsong Zhang
As one of the most important integrated nuclides for diagnosis and treatment in recent years, rhenium-188 (188Re) has a broad scope in the clinical application. Due to the specific properties of such radionuclide, it was mainly provided by the chromatographic 188W-188Re generators. There is no doubt that the application of 188Re in the treatment of various diseases depended on the development of 188W-188Re generator. Considering the high standards of such technology on radioactive activity of 188W and impurity content, a 188W-188Re generator filled with the zirconium tungstate gel has been prepared in this work. The effects of molar ratio of chemical agents, pH, reaction temperature, drying methods, rinsing methods and other conditions on the synthesis of gel particles have been studied. Furthermore, a variety of characterization techniques were used to observe the macro-/micro-morphology and chemical structure of gel particles. It can be concluded that vacuum freeze-dried method could significantly increase the specific surface area, pore size and tungsten content of gel particle. In order to decrease the content of 188W in the elute, a handful of acidic alumina was filled in the bottom of our 188W-188Re generator, an elution and purification integrated-generator was formed. During the first five processes, the nuclear purity of 188Re solution was above 99.99%, the radiochemical purity was approximately 99.5%, the pH value was 5.0–7.0 and the average elution efficiency reached up to 82.7%. In addition, the leakage rate of 188W was low as 1.60 × 10−6, and the peak of elute curve was located at 2 mL without the trailing phenomenon. This work lays a solid foundation for the domestic demand of daughter nuclide 188Re, further makes an outstanding contribution to the application of the radiation therapy technology and the protection of people's health.
铼-188(188Re)是近年来用于诊断和治疗的最重要的综合核素之一,在临床上有着广泛的应用。由于这种放射性核素的特殊性质,它主要由色谱 188W-188Re 发生器提供。毫无疑问,188Re 在各种疾病治疗中的应用取决于 188W-188Re 发生器的发展。考虑到此类技术对 188W 的放射性活度和杂质含量的高标准要求,本研究制备了填充钨酸锆凝胶的 188W-188Re 发生器。研究了化学试剂的摩尔比、pH 值、反应温度、干燥方法、漂洗方法等条件对凝胶颗粒合成的影响。此外,还采用了多种表征技术来观察凝胶颗粒的宏观/微观形态和化学结构。结果表明,真空冷冻干燥法能显著提高凝胶颗粒的比表面积、孔径和钨含量。为了降低洗脱液中 188W 的含量,我们在 188W-188Re 发生器的底部填充了一把酸性氧化铝,形成了一个洗脱和提纯一体化的发生器。在前五个过程中,188Re 溶液的核纯度均在 99.99% 以上,放射化学纯度约为 99.5%,pH 值在 5.0-7.0 之间,平均洗脱效率高达 82.7%。此外,188W 的泄漏率低至 1.60 × 10-6,且洗脱曲线的峰值位于 2 mL 处,没有拖尾现象。这项工作为满足国内对子核素188Re的需求奠定了坚实的基础,为放射治疗技术的应用和保护人民健康做出了突出贡献。
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引用次数: 0
Production of 67Cu at a biomedical cyclotron via 70Zn(p,α)67Cu reaction and its evaluation in a preclinical study using small animal SPECT/CT 在生物医学回旋加速器上通过 70Zn(p,α)67Cu 反应生产 67Cu,并在利用小动物 SPECT/CT 进行的临床前研究中对其进行评估。
IF 1.6 3区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR Pub Date : 2024-10-18 DOI: 10.1016/j.apradiso.2024.111551
Ursula Søndergaard , Kolle E. Thomas , Kristina Søborg Pedersen , Mathias Kranz , Rune Sundset , Angel Moldes-Anaya , Mikael Jensen
Clinical advancements in nuclear medicine theranostics has excited a research interest in exploring novel radionuclides for medical use. The duo of the β emitter 67Cu and the positron emitter 64Cu, has advantages over the well-established clinical pair 68Ga and 177Lu in terms of capability for high-precision therapy. Low availability has hindered the use of 67Cu whereas 64Cu has become established at a limited number of sites through production in low-to-medium energy biomedical cyclotrons. Via the reaction 70Zn(p,α)67Cu, 67Cu can also be cyclotron produced, although data on the cross sections of this reaction are sparse. Our aim in this study was three-fold: 1) to establish cross sections for relevant beam energies (14–16 MeV) of the 70Zn(p,α)67Cu reaction; 2) determine experimentally the thick target yield for 16.5 MeV proton beam; 3) establish a routine production of 67Cu for radiochemical and preclinical research. Additionally, our work aims to explore the feasibility of using biomedical cyclotrons for developing of novel therapeutic radionuclides.
Thin layers of enriched 70Zn were electrodeposited onto silver foils to employ the stacked foils technique for assessing the cross section at six energies. The thick target yield was measured experimentally using a pressed [70Zn]ZnO target. Methods were developed for solid phase extraction separation of 67Cu from the target material, as well as quality control of the product with regards to radionuclidic and radiochemical purity. Radiolabelling of PSMA-617 precursor was performed and the end product injected in a healthy mouse for a kinetic study. As a proof of concept for preclinical applications The animal was then SPECT imaged using the 185 keV gamma emission line.
Summarizing, our data confirm that biomedical cyclotrons can contribute in developing novel radionuclides, even of low cross section, for preclinical research.
核医学治疗学的临床进展激发了人们对探索新型医用放射性核素的研究兴趣。在高精度治疗能力方面,β发射体 67Cu 和正电子发射体 64Cu 的组合比临床上成熟的 68Ga 和 177Lu 组合更具优势。67Cu 的可用性较低,阻碍了它的使用,而 64Cu 则通过在中低能量生物医学回旋加速器中的生产,在有限的地点得到了应用。通过反应 70Zn(p,α)67Cu,67Cu 也可以在回旋加速器中产生,尽管有关该反应截面的数据还很稀少。我们这项研究的目的有三:1)确定 70Zn(p,α)67Cu 反应相关束能量(14-16 MeV)的截面;2)通过实验确定 16.5 MeV 质子束的厚靶产率;3)为放射化学和临床前研究建立 67Cu 的常规生产。此外,我们的工作还旨在探索利用生物医用回旋加速器开发新型治疗放射性核素的可行性。将富集的 70Zn 薄层电沉积到银箔上,采用叠箔技术评估六种能量下的横截面。使用压制的[70Zn]氧化锌靶对厚靶产量进行了实验测量。开发了从靶材料中固相萃取分离 67Cu 的方法,并对产品的放射性核素和放射化学纯度进行了质量控制。对 PSMA-617 前体进行了放射性标记,并将最终产品注射到健康小鼠体内进行动力学研究。作为临床前应用的概念验证,然后使用 185 keV 伽马发射线对动物进行 SPECT 成像。总之,我们的数据证实了生物医学回旋加速器可以为临床前研究开发新型放射性核素(即使是低截面放射性核素)做出贡献。
{"title":"Production of 67Cu at a biomedical cyclotron via 70Zn(p,α)67Cu reaction and its evaluation in a preclinical study using small animal SPECT/CT","authors":"Ursula Søndergaard ,&nbsp;Kolle E. Thomas ,&nbsp;Kristina Søborg Pedersen ,&nbsp;Mathias Kranz ,&nbsp;Rune Sundset ,&nbsp;Angel Moldes-Anaya ,&nbsp;Mikael Jensen","doi":"10.1016/j.apradiso.2024.111551","DOIUrl":"10.1016/j.apradiso.2024.111551","url":null,"abstract":"<div><div>Clinical advancements in nuclear medicine theranostics has excited a research interest in exploring novel radionuclides for medical use. The duo of the β<sup>−</sup> emitter <sup>67</sup>Cu and the positron emitter <sup>64</sup>Cu, has advantages over the well-established clinical pair <sup>68</sup>Ga and <sup>177</sup>Lu in terms of capability for high-precision therapy. Low availability has hindered the use of <sup>67</sup>Cu whereas <sup>64</sup>Cu has become established at a limited number of sites through production in low-to-medium energy biomedical cyclotrons. Via the reaction <sup>70</sup>Zn(p,α)<sup>67</sup>Cu, <sup>67</sup>Cu can also be cyclotron produced, although data on the cross sections of this reaction are sparse. Our aim in this study was three-fold: 1) to establish cross sections for relevant beam energies (14–16 MeV) of the <sup>70</sup>Zn(p,α)<sup>67</sup>Cu reaction; 2) determine experimentally the thick target yield for 16.5 MeV proton beam; 3) establish a routine production of <sup>67</sup>Cu for radiochemical and preclinical research. Additionally, our work aims to explore the feasibility of using biomedical cyclotrons for developing of novel therapeutic radionuclides.</div><div>Thin layers of enriched <sup>70</sup>Zn were electrodeposited onto silver foils to employ the stacked foils technique for assessing the cross section at six energies. The thick target yield was measured experimentally using a pressed [<sup>70</sup>Zn]ZnO target. Methods were developed for solid phase extraction separation of <sup>67</sup>Cu from the target material, as well as quality control of the product with regards to radionuclidic and radiochemical purity. Radiolabelling of PSMA-617 precursor was performed and the end product injected in a healthy mouse for a kinetic study. As a proof of concept for preclinical applications The animal was then SPECT imaged using the 185 keV gamma emission line.</div><div>Summarizing, our data confirm that biomedical cyclotrons can contribute in developing novel radionuclides, even of low cross section, for preclinical research.</div></div>","PeriodicalId":8096,"journal":{"name":"Applied Radiation and Isotopes","volume":"215 ","pages":"Article 111551"},"PeriodicalIF":1.6,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142543302","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Measurement of neutron spectra in spent fuel storage 乏燃料贮存中的中子光谱测量。
IF 1.6 3区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR Pub Date : 2024-10-18 DOI: 10.1016/j.apradiso.2024.111552
Miloš Tichý , Ondřej Huml , Tomáš Bílý , Evžen Losa , Evžen Novák , Bohumil Jánský , Jiří Rejchrt
The neutron spectrum was measured at two locations in the spent fuel storage facility of the Temelín nuclear power plant. The measurement had two primary objectives: to map the neutron -γ field by quantifying the ambient dose equivalent H∗(10) and to identify methods that could improve the quality of the adjusted neutron spectrum using a Bonner Sphere Spectrometer (BSS). Three spectrometers were used: a BSS and two proton recoil spectrometers. Hydrogen-filled proportional counters and an EJ309 scintillator were used to construct the a priori spectrum for BSS adjustment. The details of this process and its results are discussed. The a posteriori spectrum was used to calculate the ambient dose equivalent H∗(10). The resulting spectrum is highly thermalised, but the predominant contribution to H∗(10) was in the 100 keV-1.3 MeV range. The use of hydrogen-proportional counters in combination with the BSS is recommended.
在特梅林核电站乏燃料储存设施的两个地点测量了中子频谱。测量有两个主要目标:通过量化环境剂量当量 H∗(10)来绘制中子 -γ 场图,以及确定可使用邦纳球形光谱仪(BSS)提高调整后中子谱质量的方法。使用了三台光谱仪:一台 BSS 和两台质子反冲光谱仪。充氢比例计数器和 EJ309 闪烁器用于构建用于 BSS 调整的先验光谱。本文讨论了这一过程的细节及其结果。后验光谱用于计算环境剂量当量 H∗(10)。得出的光谱热化程度很高,但 H∗(10)的主要贡献在 100 keV-1.3 MeV 范围内。建议将氢比例计数器与 BSS 结合使用。
{"title":"Measurement of neutron spectra in spent fuel storage","authors":"Miloš Tichý ,&nbsp;Ondřej Huml ,&nbsp;Tomáš Bílý ,&nbsp;Evžen Losa ,&nbsp;Evžen Novák ,&nbsp;Bohumil Jánský ,&nbsp;Jiří Rejchrt","doi":"10.1016/j.apradiso.2024.111552","DOIUrl":"10.1016/j.apradiso.2024.111552","url":null,"abstract":"<div><div>The neutron spectrum was measured at two locations in the spent fuel storage facility of the Temelín nuclear power plant. The measurement had two primary objectives: to map the neutron -γ field by quantifying the ambient dose equivalent H∗(10) and to identify methods that could improve the quality of the adjusted neutron spectrum using a Bonner Sphere Spectrometer (BSS). Three spectrometers were used: a BSS and two proton recoil spectrometers. Hydrogen-filled proportional counters and an EJ309 scintillator were used to construct the a priori spectrum for BSS adjustment. The details of this process and its results are discussed. The a posteriori spectrum was used to calculate the ambient dose equivalent H∗(10). The resulting spectrum is highly thermalised, but the predominant contribution to H∗(10) was in the 100 keV-1.3 MeV range. The use of hydrogen-proportional counters in combination with the BSS is recommended.</div></div>","PeriodicalId":8096,"journal":{"name":"Applied Radiation and Isotopes","volume":"214 ","pages":"Article 111552"},"PeriodicalIF":1.6,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142456676","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Production cross sections of 102mRh and 108mAg in proton bombed natPb target with 400 MeV energy 质子轰击 400 MeV 能量的 natPb 靶件中 102mRh 和 108mAg 的产生截面。
IF 1.6 3区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR Pub Date : 2024-10-16 DOI: 10.1016/j.apradiso.2024.111533
Qi-Ze Liu , Wen-Han Dai , Ming Zeng , Zhi Zeng , V.F. Batyaev , K.V. Pavlov , A.Yu. Titarenko , Yu.E. Titarenko , R.S. Tikhonov , V.M. Zhivun
The accelerator-driven subcritical system (ADS) is a competitive option for next-generation nuclear energy systems. Production cross sections of long-lived residual radioactive nuclides in a proton-nuclide reaction are basic quantities for the calculation of accumulated radioactivity in the use of ADS systems. This work presents the production cross sections of 102mRh and 108mAg in a natural lead (natPb) target activated by 400 MeV protons. The natPb target was irradiated by a 400 MeV proton beam in NRC “Kurchatov Institute” and measured two decades later by a low background gamma spectrometer in China Jinping Underground Laboratory (CJPL). A spectrum analysis method based on simulated single-isotope spectrum and Bayesian peak fitting was employed to compute the activities and production cross sections of the residual nuclides. The experimentally measured cross-sections for 102mRh and 108mAg were 0.72 ± 0.05 mb and 0.76 ± 0.09 mb respectively. These values are approximately twice as high as those predicted by the QGSP_INCLXX_HP model and fall within the range predicted by the INCL4+ABLA and LAQGSM+GEM2 models for mass numbers A=102 and A=108. These findings offer new experimental insights for ADS research and provide a practical benchmark for theoretical models concerning proton-lead interactions.
加速器驱动的亚临界系统(ADS)是下一代核能系统的一个具有竞争力的选择。质子-核素反应中长寿命残余放射性核素的生成截面是计算使用 ADS 系统时累积放射性的基本量。本研究介绍了 102mRh 和 108mAg 在被 400 MeV 质子激活的天然铅(natPb)靶中的产生截面。natPb 靶是在国家核研究中心 "库尔恰托夫研究所 "用 400 兆电子伏质子束辐照的,二十年后在中国锦屏地下实验室用低本底伽马能谱仪进行了测量。采用基于模拟单同位素谱和贝叶斯峰拟合的谱分析方法,计算了残余核素的放射性活度和生成截面。实验测得的102mRh和108mAg的截面分别为0.72 ± 0.05 mb和0.76 ± 0.09 mb。这些值大约是 QGSP_INCLXX_HP 模型预测值的两倍,并且在 INCL4+ABLA 和 LAQGSM+GEM2 模型预测的质量数 A=102 和 A=108 的范围内。这些发现为 ADS 研究提供了新的实验见解,并为质子-铅相互作用的理论模型提供了实用基准。
{"title":"Production cross sections of 102mRh and 108mAg in proton bombed natPb target with 400 MeV energy","authors":"Qi-Ze Liu ,&nbsp;Wen-Han Dai ,&nbsp;Ming Zeng ,&nbsp;Zhi Zeng ,&nbsp;V.F. Batyaev ,&nbsp;K.V. Pavlov ,&nbsp;A.Yu. Titarenko ,&nbsp;Yu.E. Titarenko ,&nbsp;R.S. Tikhonov ,&nbsp;V.M. Zhivun","doi":"10.1016/j.apradiso.2024.111533","DOIUrl":"10.1016/j.apradiso.2024.111533","url":null,"abstract":"<div><div>The accelerator-driven subcritical system (ADS) is a competitive option for next-generation nuclear energy systems. Production cross sections of long-lived residual radioactive nuclides in a proton-nuclide reaction are basic quantities for the calculation of accumulated radioactivity in the use of ADS systems. This work presents the production cross sections of <sup>102m</sup>Rh and <sup>108m</sup>Ag in a natural lead (<sup>nat</sup>Pb) target activated by 400 MeV protons. The <sup>nat</sup>Pb target was irradiated by a 400 MeV proton beam in NRC “Kurchatov Institute” and measured two decades later by a low background gamma spectrometer in China Jinping Underground Laboratory (CJPL). A spectrum analysis method based on simulated single-isotope spectrum and Bayesian peak fitting was employed to compute the activities and production cross sections of the residual nuclides. The experimentally measured cross-sections for <sup>102m</sup>Rh and <sup>108m</sup>Ag were 0.72 ± 0.05 mb and 0.76 ± 0.09 mb respectively. These values are approximately twice as high as those predicted by the QGSP_INCLXX_HP model and fall within the range predicted by the INCL4+ABLA and LAQGSM+GEM2 models for mass numbers A=102 and A=108. These findings offer new experimental insights for ADS research and provide a practical benchmark for theoretical models concerning proton-lead interactions.</div></div>","PeriodicalId":8096,"journal":{"name":"Applied Radiation and Isotopes","volume":"214 ","pages":"Article 111533"},"PeriodicalIF":1.6,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142493528","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The adsorption of cesium by sulfonic acid functionalized hollow mesoporous silica microspheres 磺酸功能化中空介孔二氧化硅微球对铯的吸附
IF 1.6 3区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR Pub Date : 2024-10-15 DOI: 10.1016/j.apradiso.2024.111554
Wei Jiang , Xixiang Yue , Sili Chen , Zhengke Zhang , Ji Wang , Jinsong Wang
With the development of nuclear industry, radioactive elements such as 137Cs put a threat on the water environment. It is a challenging task to remove the Cs+ in the nuclear wastewater. In the current study, we prepared a new Cs+-adsorbing material by introducing sulfhydryl group onto the surface of hollow mesoporous silica microspheres, then oxidizing the sulfhydryl group to sulfonic acid group. The obtained HMSS-SO3H material had an excellent adsorption capacity for Cs+ in the aqueous solution, with an adsorption capacity of 51.53 mg g−1 in 30 min. Characterization approaches, such as FT-IR and EDS, were used to confirm the result of modification. Adsorption experiments were carried out under. The influence of various parameters on the adsorption process was investigated under the conditions of changing pH, temperature, and time. The effect of competitive ions was also explored. The results indicated that the adsorption process followed the pseudo-second-order model and the main adsorption mechanisms are electrostatic interaction and coordination. The material had a best adsorption performance at a neutral pH. The adsorption process could well-fit the Langmuir's model, with a theoretical maximum adsorption capacity of 81.31 mg g−1. And the adsorption capacity was slightly affected by competing ions such as Mg2+ and Ca2+. The results indicate that the HMSS-SO3H prepared in this study is a promising adsorbent for Cs+, with the advantages of high adsorption capacity, fast adsorption rate and high selectivity.
随着核工业的发展,137Cs 等放射性元素对水环境造成了威胁。如何去除核废水中的 Cs+ 是一项具有挑战性的任务。在本研究中,我们在中空介孔二氧化硅微球表面引入巯基,然后将巯基氧化为磺酸基,制备了一种新型 Cs+ 吸附材料。得到的 HMSS-SO3H 材料对水溶液中的 Cs+ 具有极佳的吸附能力,30 分钟内的吸附量为 51.53 mg g-1。傅立叶变换红外光谱(FT-IR)和 EDS 等表征方法证实了改性结果。在以下条件下进行了吸附实验。在改变 pH 值、温度和时间的条件下,研究了各种参数对吸附过程的影响。还探讨了竞争性离子的影响。结果表明,吸附过程遵循伪二阶模型,主要的吸附机理是静电作用和配位作用。该材料在中性 pH 条件下具有最佳的吸附性能。吸附过程完全符合 Langmuir 模型,理论最大吸附容量为 81.31 mg g-1。吸附容量受 Mg2+ 和 Ca2+ 等竞争离子的影响较小。结果表明,本研究制备的 HMSS-SO3H 是一种很有前途的 Cs+ 吸附剂,具有吸附容量大、吸附速率快和选择性高等优点。
{"title":"The adsorption of cesium by sulfonic acid functionalized hollow mesoporous silica microspheres","authors":"Wei Jiang ,&nbsp;Xixiang Yue ,&nbsp;Sili Chen ,&nbsp;Zhengke Zhang ,&nbsp;Ji Wang ,&nbsp;Jinsong Wang","doi":"10.1016/j.apradiso.2024.111554","DOIUrl":"10.1016/j.apradiso.2024.111554","url":null,"abstract":"<div><div>With the development of nuclear industry, radioactive elements such as <sup>137</sup>Cs put a threat on the water environment. It is a challenging task to remove the Cs<sup>+</sup> in the nuclear wastewater. In the current study, we prepared a new Cs<sup>+</sup>-adsorbing material by introducing sulfhydryl group onto the surface of hollow mesoporous silica microspheres, then oxidizing the sulfhydryl group to sulfonic acid group. The obtained HMSS-SO<sub>3</sub>H material had an excellent adsorption capacity for Cs<sup>+</sup> in the aqueous solution, with an adsorption capacity of 51.53 mg g<sup>−1</sup> in 30 min. Characterization approaches, such as FT-IR and EDS, were used to confirm the result of modification. Adsorption experiments were carried out under. The influence of various parameters on the adsorption process was investigated under the conditions of changing pH, temperature, and time. The effect of competitive ions was also explored. The results indicated that the adsorption process followed the pseudo-second-order model and the main adsorption mechanisms are electrostatic interaction and coordination. The material had a best adsorption performance at a neutral pH. The adsorption process could well-fit the Langmuir's model, with a theoretical maximum adsorption capacity of 81.31 mg g<sup>−1</sup>. And the adsorption capacity was slightly affected by competing ions such as Mg<sup>2+</sup> and Ca<sup>2+</sup>. The results indicate that the HMSS-SO<sub>3</sub>H prepared in this study is a promising adsorbent for Cs<sup>+</sup>, with the advantages of high adsorption capacity, fast adsorption rate and high selectivity.</div></div>","PeriodicalId":8096,"journal":{"name":"Applied Radiation and Isotopes","volume":"214 ","pages":"Article 111554"},"PeriodicalIF":1.6,"publicationDate":"2024-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142444973","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development of a silicon carbide radiation detection system and experimentation of the system performance 开发碳化硅辐射探测系统并进行系统性能实验
IF 1.6 3区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR Pub Date : 2024-10-15 DOI: 10.1016/j.apradiso.2024.111555
Jinlin Song , Xiaobin Tang , Pin Gong , Zhimeng Hu , Dajian Liang , Zeyu Wang , Peng Wang , Hong Ying , Haining Shi , Ao Liu , Zhifei Zhao , Song Bai
Silicon carbide (SiC) detectors have excellent radiation detection capabilities for various radiation particles, including high energy resolution, fast response times, and good radiation resistance. A SiC radiation detection system was developed to measure the neutron fluence rate and the γ-ray dose rate in high intensity radiation fields. The system was composed of two SiC detectors, a temperature monitor, two preamplifiers for each SiC detector, a data acquisition unit with two signal channels, three pairs of communication devices, and an application software to analyze and visualize the measurement data. The two SiC detectors were fabricated based on two kinds of 4H-SiC diodes and used to respectively respond to neutrons and γ-rays. Repeated experiments showed that the two SiC detectors of the system can respond to α-particles, neutrons, and γ-rays. To verify the performance of the SiC detection system, including the response linearity of the neutron fluence rate, the measurement range of the γ-ray dose rate, and the radiation resistance of the SiC radiation detectors, the system was tested in multiple neutron and γ-ray fields. The tests results show the system can measure the neutron fluence rate from 5.64 × 10 2 cm−2 s−1 to 1.03 × 10 5 cm−2 s−1 with excellent linearity response, and the γ-ray dose rate from 0.005 Gy/h to 20 Gy/h. Furthermore, the SiC detectors demonstrated good radiation resistance. The neutron and γ-ray radiation field can still be measured stably by the system after exposure to neutron fluence of 1.07 × 10 14 cm−2 and γ-ray dose of 3.52 × 10 4 Gy. This work is the preliminary research to continue the exploration how to measure the n/γ hybrid fields accurately using SiC detectors considering the different energy of neutrons.
碳化硅(SiC)探测器对各种辐射粒子具有出色的辐射探测能力,包括高能量分辨率、快速响应时间和良好的抗辐射能力。我们开发了一种碳化硅辐射探测系统,用于测量高强度辐射场中的中子通量率和γ射线剂量率。该系统由两个碳化硅探测器、一个温度监测器、每个碳化硅探测器的两个前置放大器、一个具有两个信号通道的数据采集单元、三对通信设备以及一个用于分析和显示测量数据的应用软件组成。两个 SiC 探测器是基于两种 4H-SiC 二极管制造的,分别用于响应中子和 γ 射线。反复的实验表明,该系统的两个 SiC 探测器可以对 α 粒子、中子和 γ 射线做出响应。为了验证 SiC 检测系统的性能,包括中子通量率的响应线性、γ 射线剂量率的测量范围以及 SiC 辐射探测器的抗辐射能力,该系统在多个中子和γ 射线场中进行了测试。测试结果表明,该系统可测量 5.64 × 10 2 cm-2 s-1 至 1.03 × 10 5 cm-2 s-1 的中子通量率,线性响应极佳;可测量 0.005 Gy/h 至 20 Gy/h 的γ射线剂量率。此外,碳化硅探测器还具有良好的抗辐射能力。该系统在受到 1.07 × 10 14 cm-2 的中子通量和 3.52 × 10 4 Gy 的γ射线剂量照射后,仍能稳定地测量中子和γ射线辐射场。这项工作是继续探索如何利用碳化硅探测器准确测量不同能量中子的 n/γ 混合场的初步研究。
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引用次数: 0
Fabrication of polymeric shields to attenuation ionizing radiation and a flame retardant supported by nano-bismuth oxide prepared by co-deposition 用共沉积法制备的纳米氧化铋和阻燃剂制作可衰减电离辐射的聚合物防护罩
IF 1.6 3区 工程技术 Q3 CHEMISTRY, INORGANIC & NUCLEAR Pub Date : 2024-10-13 DOI: 10.1016/j.apradiso.2024.111556
Shaymaa Mohammed Fayyadh , Ali Ben Ahmed
The results of the preparation of protective shields from ionizing radiation, flame retardant from pure epoxy supported by nano-bismuth oxide, show that the protective shields supported by nanoparticles improve the attenuation properties, the thermal stability, the flame retardancy and mechanical properties. Also, the polymeric shield supported by Bi2O3 (Na2CO3) retardant the flame much better than supported by Bi2O3 (NaOH). Finally, the quality of the protective shields increased as the energy of the photons of the ionizing rays decreased.
纳米氧化铋支撑的纯环氧阻燃电离辐射防护罩的制备结果表明,纳米粒子支撑的防护罩在衰减性能、热稳定性、阻燃性和机械性能方面都有所改善。此外,Bi2O3(Na2CO3)支撑的聚合物防护罩的阻燃性能比 Bi2O3(NaOH)支撑的防护罩好得多。最后,保护罩的质量随着电离辐射光子能量的降低而提高。
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引用次数: 0
期刊
Applied Radiation and Isotopes
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