痕量单一价态钚溶液的制备
建立了痕量Pu(Ⅳ)、Pu(Ⅴ)、Pu(Ⅵ)溶液的制备方法,并跟踪了各价态钚溶液的稳定性.采用TTA选择性萃取Pu(Ⅳ)、HDEHP萃取Pu(Ⅳ+Ⅵ)的方法分析了溶液中钚价态的分布.结果表明,将浓度为1011mol/L量级的钚溶液在1 mol/L HNO3体系中反复蒸干可制得Pu(Ⅳ)溶液;Pu(Ⅳ)在0.5~1 mol/L HNO30.1 mmol/L KMnO4溶液体系中反应24 h,可获得Pu(Ⅵ)溶液;Pu(Ⅵ)避光保存5d后,可得到Pu(Ⅴ)溶液,各单一价态钚溶液的纯度均大于90%.在pH=3.0、0.01mol/L NaCl体系中,各价态均不能稳定存在,因此,所需单一价态钚溶液应新...
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Published in | 核化学与放射化学 Vol. 36; no. 4; pp. 200 - 204 |
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Main Author | |
Format | Journal Article |
Language | Chinese |
Published |
西北核技术研究所,陕西西安710024%西北核技术研究所,陕西西安,710024%兰州大学 放射化学研究所,甘肃兰州,730000
2014
兰州大学 放射化学研究所,甘肃兰州 730000 |
Subjects | |
Online Access | Get full text |
ISSN | 0253-9950 |
DOI | 10.7538/hhx.YX.2014.2013064 |
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Summary: | 建立了痕量Pu(Ⅳ)、Pu(Ⅴ)、Pu(Ⅵ)溶液的制备方法,并跟踪了各价态钚溶液的稳定性.采用TTA选择性萃取Pu(Ⅳ)、HDEHP萃取Pu(Ⅳ+Ⅵ)的方法分析了溶液中钚价态的分布.结果表明,将浓度为1011mol/L量级的钚溶液在1 mol/L HNO3体系中反复蒸干可制得Pu(Ⅳ)溶液;Pu(Ⅳ)在0.5~1 mol/L HNO30.1 mmol/L KMnO4溶液体系中反应24 h,可获得Pu(Ⅵ)溶液;Pu(Ⅵ)避光保存5d后,可得到Pu(Ⅴ)溶液,各单一价态钚溶液的纯度均大于90%.在pH=3.0、0.01mol/L NaCl体系中,各价态均不能稳定存在,因此,所需单一价态钚溶液应新鲜制备. |
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Bibliography: | 11-2045/TL plutonium;trace level;single oxidation state;preparation The trace levels of single oxidation state plutonium(Pu(Ⅳ, V , Ⅵ )) solution was prepared, and the stability was monitored over time. The oxidation state distribution of the solution was analyzed by solvent extraction methods, in which Pu(IV) was extracted with TTA and Pu (Ⅳ + Ⅵ) was separated by HDEHP. The Pu (Ⅳ) solution is prepared by heating the solution until dryness in 1 mol/L HNO3 repeatedly, and Pu(Ⅵ) solution is obtained by keeping Pu (Ⅳ) in 0.5-1 mol/L HNO3-0. 1 mmol/L KMnO4 system for 24 h. Pu(Ⅵ) is reduced automatically to Pu( V ) in the dark for 5 d. All of these single plutonium solutions could not keep steady in pH=3.0, 0.01 mol/L NaC1 system. Consequently, single oxidation state plutonium solutions need to be prepared freshly for each experiment. WANG Yu, HAN Xiao-yuan, ZHANG Rui-rong, ZHOU Xu, LIU Yan, WU Wang-suo( 1. Radiochemistry Laboratory, School of Nuclear Science and Technology, Lanzhou University, Lanzhou 730000, China;2 |
ISSN: | 0253-9950 |
DOI: | 10.7538/hhx.YX.2014.2013064 |