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首页> 外文期刊>Radiochimica Acta: International Journal for Chemical Aspects of Nuclear Science and Technology >Development of methods for the preparation of radiopure 82Se sources for the SuperNEMO neutrinoless double-beta decay experiment
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Development of methods for the preparation of radiopure 82Se sources for the SuperNEMO neutrinoless double-beta decay experiment

机译:制备放射性82SE源的制备方法,用于超中子源双β衰变实验的源

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摘要

A radiochemical method for producing 82Se sources with an ultra-low level of contamination of natural radionuclides (40K, decay products of 232Th and 238U) has been developed based on cation-exchange chromatographic purification with reverse removal of impurities. It includes chromatographic separation (purification), reduction, conditioning (which includes decantation, centrifugation, washing, grinding, and drying), and 82Se foil production. The conditioning stage, during which highly dispersed elemental selenium is obtained by the reduction of purified selenious acid (H2SeO3) with sulfur dioxide (SO2) represents the crucial step in the preparation of radiopure 82Se samples. The natural selenium (600 g) was first produced in this procedure in order to refine the method. The technique developed was then used to produce 2.5 kg of radiopure enriched selenium (82Se). The produced 82Se samples were wrapped in polyethylene (12 μm thick) and radionuclides present in the sample were analyzed with the BiPo-3 detector. The radiopurity of the plastic materials (chromatographic column material and polypropylene chemical vessels), which were used at all stages, was determined by instrumental neutron activation analysis. The radiopurity of the 82Se foils was checked by measurements with the BiPo-3 spectrometer, which confirmed the high purity of the final product. The measured contamination level for 208Tl was 8–54 μBq/kg, and for 214Bi the detection limit of 600 μBq/kg has been reached.
机译:基于阳离子交换色谱纯化,开发了具有超低污染的82SE污染的82SE来源的放射化学方法,其基于阳离子交换色谱纯化,反向除去杂质。它包括色谱分离(纯化),还原,调节(包括倾析,离心,洗涤,研磨和干燥)和82se箔产生。通过二氧化硫(SO 2)的纯化的硒酸(H 2 SeO3)还原通过二氧化硫(SO 2)来获得调节阶段,该阶段通过二氧化硫(SO 2)表示在放射82SE样品的制备中的关键步骤。本程序首先首先生产天然硒(600g),以便改进该方法。然后使用该技术用于产生2.5kg富含富集硒(82se)的放射性物质。将产生的82SE样品包裹在聚乙烯(12μm厚)中,并用BIPO-3检测器分析样品中存在的放射性核素。通过仪器中子激活分析确定在所有阶段使用的塑料材料(色谱柱材料和聚丙烯化学容器)的放射性。通过使用BIPO-3光谱仪进行测量检查82SE箔的辐射度,证实了最终产品的高纯度。 208T1的测量污染水平为8-54μBQ/ kg,并且已经达到了214bi,检测限为600μbq/ kg。

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