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Comparison of Two Sample Preparation Methods for X-Ray Fluorescence Spectrometry in the Determination of Ni and Cr

机译:X射线荧光光谱法测定镍和铬的两种样品制备方法的比较

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摘要

Pressed powder pellets and fused beads or glass disks are routinely used in X-ray fluorescence spectrometry for the determination of major and trace elements, respectively, in geological materials. In order to evaluate the performance of these two sample preparation methods, we determined Ni and Cr concentrations of fourteen RMs from Japan, France and South Africa, and eighty-five igneous and three sedimentary rock samples from Mexico in both powder pellets and glass beads. We also computed new values of statistical parameters for RMs from an outlier-based multiple-test method and compared them with the literature mean and confidence limit values. The results showed that the multiple-test method provided more reliable central tendency and dispersion parameters for RMs than those obtained previously from the two or three standard deviation method, or from robust methods. The powder pellet and fused bead sample preparation methods provided consistent results for Ni and Cr at concentration levels > 50 lg g~(-1) in this application; for lower concentration levels, however, these methods showed somewhat greater differences. For quantitative comparisons, both ordinary and weighted least-squares linear regression models were used to show that the two sample preparation methods provided generally unbiased results.
机译:在X射线荧光光谱法中通常使用压制的粉末颗粒和熔融珠或玻璃片分别测定地质材料中的主要元素和痕量元素。为了评估这两种样品制备方法的性能,我们确定了来自日本,法国和南非的14个RMs以及来自墨西哥的85个火成岩样品和3个沉积岩样品在粉末颗粒和玻璃珠中的Ni和Cr浓度。我们还通过基于异常值的多重检验方法计算了RM的统计参数新值,并将其与文献中的均值和置信度极限值进行了比较。结果表明,与先前从二,三标准偏差方法或鲁棒性方法获得的结果相比,多重测试方法为RM提供了更可靠的集中趋势和分散参数。在本应用中,粉末颗粒和熔珠样品制备方法对浓度> 50 lg g〜(-1)的镍和铬提供了一致的结果。对于较低的浓度水平,这些方法显示出较大的差异。为了进行定量比较,使用普通最小二乘法和加权最小二乘线性回归模型来显示两种样品制备方法通常提供无偏结果。

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