首页> 外文期刊>Journal of Radioanalytical and Nuclear Chemistry: An International Journal Dealing with All Aspects and Applications of Nuclear Chemistry >Sequential isotopic determination of plutonium, thorium, americium and uranium in the air filter and drinking water samples around the WIPP site
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Sequential isotopic determination of plutonium, thorium, americium and uranium in the air filter and drinking water samples around the WIPP site

机译:WIPP站点周围空气过滤器和饮用水样品中of,th,a和铀的同位素检测

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摘要

The simultaneous determination of actinides in air filter and water samples around the WIPP site have been demonstrated. The analytical method is based on the selective separation and purification by anion exchange and Eichrome-TEVA, TRU and DGA-resin followed by determination of actinides by alpha spectrometry. Counting sources for alpha spectrometric measurements were prepared by microcoprecipitation on neodymium fluoride (NdF_3). Radiochemical yields were determined using ~(242)Pu, ~(229)Th, ~(243)Am and ~(232)U as tracers. The validation of the method is performed through the analysis of reference materials or participating in laboratory intercomparison programs. The plutonium concentrations in aerosols varied seasonally, being highest in spring and summer due to the spring-time enhanced wind-storm transportation of radioactive aerosols from the stratosphere to the troposphere. The ~(238)Pu/~(239)+~(240)Pu activity ratio in the aerosol samples is typically close to that of global fallout from historic above-ground nuclear weapons testing. The results presented here indicate that the source of plutonium in the WIPP environment results mainly from global nuclear fallout and there is no evidence of increases in radiological contaminants in the region that could be attributed to releases from the WIPP.
机译:已经证明了同时测定WIPP站点周围空气过滤器和水样中of系元素的含量。该分析方法基于通过阴离子交换和Eichrome-TEVA,TRU和DGA-树脂的选择性分离和纯化,然后通过α光谱测定determination系元素。通过在氟化钕(NdF_3)上进行微共沉淀制备用于α光谱测量的计数源。使用〜(242)Pu,〜(229)Th,〜(243)Am和〜(232)U作为示踪剂测定放射化学产率。该方法的验证是通过分析参考材料或参加实验室比对程序来进行的。气溶胶中p的浓度随季节变化,春季和夏季最高,这是由于春季的放射性气溶胶从平流层到对流层的春季暴风雨运输增加。气溶胶样品中的〜(238)Pu /〜(239)+〜(240)Pu活度比通常接近历史性地上核武器试验的全球沉降量。这里提供的结果表明,WIPP环境中的the源主要来自全球核辐射,并且没有证据表明该地区放射性污染物的增加可能归因于WIPP的释放。

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