Improving clinical laboratory performance through quality indicators

等压线 加速器质谱 质谱法 化学 离子 二次离子质谱法 同位素 自然丰度 分析化学(期刊) 多原子离子 核物理学 环境化学 物理 色谱法 核子 有机化学
作者
Magdalena Krintus,Mario Plebani,Mauro Panteghini
出处
期刊:Clinical Biochemistry [Elsevier BV]
卷期号:50 (10-11): 547-549 被引量:2
标识
DOI:10.1016/j.clinbiochem.2017.05.006
摘要

Secondary ion mass spectrometry (SIMS) provides spatially resolved trace analysis of solid materials, but can be complicated by unresolved abundant molecular isobars. By adding a 300-kV single-stage accelerator mass spectrometer (SSAMS) as a detector for a Cameca ims 4f SIMS, one can measure more abundant positive ions from the SIMS while removing molecular isobars, thus improving very low abundance trace element and isotope analysis. This paper describes important features and capabilities of such an integrated system at the Naval Research Laboratory using charge state +1 ions. Transmission loss is compared to molecule destruction as gas flow to the molecule-destruction cell increases. As most measurements tolerate more modest abundance sensitivities than for 14C analysis, a lower gas flow is acceptable, so good transmission of 20–50% for ions of interest can be maintained for a broad range of ion masses. This new instrument has measured isotope ratios for uranium, lead, rare earths, and other elements from particulates and localized regions, with molecule destruction enabling the measurement at low SIMS mass resolving power and thus high transmission, as examples will show. This new and world-unique instrument provides improved capabilities for applications in nuclear and other forensics, geochemistry, cosmochemistry, and the development of optical, electronic, multifunctional, and structural materials.
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