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首页> 外文期刊>Current Analytical Chemistry >Radiochemical Separation and Anti-Compton Analysis of Ni, Sn, Te and Zn in Lead Standard Reference Materials at Ultra-Trace Levels
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Radiochemical Separation and Anti-Compton Analysis of Ni, Sn, Te and Zn in Lead Standard Reference Materials at Ultra-Trace Levels

机译:铅标准参考物质中超痕量水平的镍,锡,碲和锌的放射化学分离和反康顿分析

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In this work results are reported on the determination of some elements, Ni, Sn, Te and Zn, present at ultra-trace levels (ng g~(-1)) in three different samples of metallurgical lead, i.e. electrolytically refined lead, thermally refined lead and lead with added impurities, assigned to be employed as standard reference materials by BCR. The Instrumental Neutron Activation Analysis was used for its characteristics to be a primary analytical method and for reaching high sensitivity and accuracy. The y-spectrometry measurements have been performed by means of a counter system operating in anticoincidence; for the Sn and Te measures a radiochemical separation of the main interfering radionuclides was necessary. The irradiation was performed in the central channel of the Triga Mark II reactor of the R.C.-Casaccia, ENEA, at a neutron flux of 2.68X10~(13) nXcm~(-2)Xs~(-1); the irradiation time was protracted to reach a total integrated flux of 2X10~(19) nXcm~(-2). In this way, 42.2 ng g~(-1) of Ni, 1.7 ng g~(-1) of Sn, 7.6 ng g~(-1) of Te and 35.5 ng g~(-1) of Zn in the Electrolytically Refined Lead and 24.2 ng g~(-1) of Ni, 5.7 ng g~(-1) of Sn, 8.2 ng g~(-1) of Te and 18.5 ng g~(-1) of Zn in the Thermally Refined Lead, respectively, were measured. The third sample was used as reference: it was obtained by adding impurities to a Thermally Refined Lead. In this case each element was present at (mu)g g~(-1) level. It should be underlined that for some elements at ultra-trace levels (i.e. Ni, Sn and Te) only few measurements were useful in the relative certification: in particular, only using a radiochemical separation and an anti-Compton suppression a very low limit of detection was reached.
机译:在这项工作中,报告了测定三种不同冶金铅样品(电解精炼铅)中超痕量水平(ng g〜(-1))中某些元素镍,锡,碲和锌的测定结果。精炼铅和添加了杂质的铅,被BCR指定用作标准参考材料。使用仪器中子活化分析是因为其特性是一种主要的分析方法,并且可以达到很高的灵敏度和准确性。 y光谱测量是通过反巧合运行的计数系统完成的。对于Sn和Te措施,必须对主要干扰放射性核素进行放射化学分离。辐照在中子通量为2.68X10〜(13)nXcm〜(-2)Xs〜(-1)的R.C.-Casaccia,ENEA的Triga Mark II反应器的中央通道中进行;照射时间延长至总积分通量为2X10〜(19)nXcm〜(-2)。这样,电解中的镍为42.2 ng g〜(-1),锡1.7 ng g〜(-1),Te 7.6 ng g〜(-1),锌35.5 ng g〜(-1)。热精炼中的精炼铅和24.2 ng g〜(-1)的镍,5.7 ng g〜(-1)的锡,8.2 ng g〜(-1)的Te和18.5 ng g〜(-1)的锌分别测量铅。第三个样品用作参考:通过将杂质添加到热精制铅中获得。在这种情况下,每种元素以μgg〜(-1)的水平存在。应该强调的是,对于某些超痕量水平的元素(例如,Ni,Sn和Te),只有很少的测量可用于相对认证:特别是,仅使用放射化学分离和抗康普顿抑制时,其极低的限量检测到。

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