特里加
硝酸铀酰
放射化学
铀
辐照
硝酸盐
裂变产物
放射性核素
研究堆
化学
核裂变产物
质谱法
中子
核化学
核工程
材料科学
核物理学
色谱法
冶金
物理
有机化学
工程类
作者
Fatum Rahmana Putra,Syarip Syarip,Sihana Sihana
标识
DOI:10.1016/j.nucengdes.2023.112701
摘要
Different Uranyl Nitrate Solution concentrations and undiluted Uranyl Nitrate Hexahydrate were irradiated in the Kartini TRIGA Mk II reactor to qualitatively assess the radioisotope production feasibility in different neutron fluxes within reactor irradiation facilities. Multiple radioisotope gamma spectrums’ were obtained using the Neutron Activation Analysis method without chemical separation prior to detection. The presented methodology serves as a preliminary experiment toward the Subcritical Assembly for 99Mo Production (SAMOP) application in the Kartini reactor. The results show that the concentration and crystallization of Uranyl Nitrate can change the detectability of some radioisotopes in gamma spectrometry. Through a combination of depletion calculation and standardized measurement, some dominant isotopes’ gamma peaks from irradiated Uranyl Nitrate are identifiable, and their activity is quantifiable. Although chemical separation is inseparable from fission product analysis using gamma spectrometry, the presented direct measurement establishes a practical and rapid assessment method for the next isotope production development in the Kartini reactor.
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