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Porous iron pellets for AMS ~(14)C analysis of small samples down to ultra-microscale size (10-25 μgC)

机译:多孔铁丸用于AMS〜(14)C分析小尺寸超小尺寸(10-25μgC)的样品

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We developed the use of a porous iron pellet as a catalyst for AMS ~(14)C analysis of small samples down to ultra-microscale size (10-25 μgC). It resulted in increased and more stable beam currents through our HVEE 4130 ~(14)C AMS system, which depend smoothly on the sample size. We find that both the expected decrease of oxalic acid standards and increase of backgrounds with decreasing sample size, due to increasing influence of contamination, are reproducible. Using a mass-dependent background correction for dead (1.0 ± 0.4 μgC) and modern (0.25 ± 0.10 μgC) contamination, we obtain reliable results for small samples down to 10 μgC and possibly smaller. Due to our low graphitization yield for ultra-small samples (increases from 40% to 80% on average with sample size), we measured graphite standards as small as 3 μgC. The standard deviation of the corrected activity is about 5% for a 10-μgC HOxII standard.rnHere we report the iron pellet technique, which is new to the best of our knowledge. It is generally applicable for AMS ~(14)C laboratories that want to measure small samples down to ultra-microscale size. As an illustrative test-case, we analyze ~(14)C data for IAEA-C5, C7 and C8 samples with masses ranging from 15 to 300 μgC.
机译:我们开发了使用多孔铁丸作为催化剂,对小至超微尺寸(10-25μgC)的小样品进行AMS〜(14)C分析。通过我们的HVEE 4130〜(14)C AMS系统,光束电流增加且更稳定,这取决于样本量。我们发现,由于污染影响的增加,草酸标准品的预期降低和背景的增加(随着样本量的减少)都是可重现的。使用针对死点(1.0±0.4μgC)和现代(0.25±0.10μgC)污染的质量相关背景校正,对于低至10μgC甚至可能更小的小样本,我们可以获得可靠的结果。由于我们的超小型样品石墨化产率低(样品量平均增加40%至80%),因此我们测量的石墨标准液小至3μgC。对于10μgCHOxII标准品,校正后的活性的标准偏差约为5%。在此,我们报道了铁丸技术,这是我们所知的最新技术。它通常适用于AMS〜(14)C实验室,该实验室要测量小至超微尺寸的样品。作为一个说明性的测试案例,我们分析了质量为15至300μgC的IAEA-C5,C7和C8样品的〜(14)C数据。

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