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首页> 外文期刊>Journal of Radioanalytical and Nuclear Chemistry: An International Journal Dealing with All Aspects and Applications of Nuclear Chemistry >Alternative chromatographic processes for no-carrier added Lu-177 radioisotope separation - Part II. The conventional column chromatographic separation combined with HPLC for high purity
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Alternative chromatographic processes for no-carrier added Lu-177 radioisotope separation - Part II. The conventional column chromatographic separation combined with HPLC for high purity

机译:无载体添加Lu-177放射性同位素分离的替代色谱方法-第II部分。常规柱色谱分离与HPLC相结合可实现高纯度

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摘要

HPLC technique combined with the simple conventional column solid phase extraction (SPE) chromatography using di-(2-ethylhexyl)orthophosphoric acid (HDEHP) impregnated OASIS-HLB sorbent based SPE resins (OASIS-HDEHP) was developed for the separation of no-carrier added (n.c.a) Lu-177 from the bulk quantity of ytterbium target. This combination strategy was based on combining the advantages of the better resolution of HPLC separation of n.c.a Lu-177 from the few milligram level Yb target with the high capacity of the OASIS-HDEHP column for the separation of Lu-177 from the bulk Yb target. The production batches of several hundred mCi activity of n.c.a Lu-177 radioisotope separated from 50 mg Yb target activated in a nuclear reactor of medium neutron flux (Phi = 5 center dot 10(13) n.cm(-2).s(-1)) were successfully performed using this combined separation technique. With the target irradiation in a reactor of higher thermal neutron flux or with the parallel run of several separation units, several Ci-s of n.c.a Lu-177 can be profitably produced on a commercial production basis.
机译:HPLC技术结合简单的常规柱固相萃取(SPE)色谱法,使用二(2-乙基己基)正磷酸(HDEHP)浸渍的OASIS-HLB吸附剂基SPE树脂(OASIS-HDEHP)进行了分离从大量target靶中添加了(nca)Lu-177。这种组合策略是基于以下优点:将HPLC分离出数毫克水平Yb靶标的nca Lu-177的HPLC分离度更高,而OASIS-HDEHP柱具有将Lu-177与散装Yb靶标分离的高分离度的优点。从中等中子通量(Phi = 5中心点10(13)n.cm(-2).s(-)的核反应堆中活化的50 mg Yb靶标分离的nca Lu-177放射性同位素的生产批次具有数百mCi活性1))使用此组合分离技术成功进行。在高中子热通量的反应堆中进行目标照射或几个分离单元的平行运行,可以商业化生产n.c. a Lu-177的几个Ci-s。

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