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The application of X-rays to the analysis of materials can take forms other than X-ray fluorescence. In X-ray absorption spectrometry, the ability of a sample to absorb radiation from an X-ray source is measured. Absorption follows Beer's law (see Section 12.1) and, compared to emission, is relatively free of matrix effects. X-ray absorption, however, is a less selective technique than atomic fluorescence because we are not measuring the emission from an analyte's characteristic lines. X-ray absorption finds its greatest utility for the quantitative analysis of samples that contain just one or two major analytes.
In powder X-ray diffraction we focus the radiation from an X-ray tube line source on a powdered sample and measure the intensity of diffracted radiation as a function of the transducer's angle (\(2 \theta\)). A typical powder X-ray diffraction spectrum is in Figure \(\PageIndex{1}\) for the mineral calcite (CaCO3). Qualitative identification is obtained by matching the \(2 \theta\) peaks to those in published databases. A quantitative analysis for the compound—not the elements that make up the compound—is possible using the intensity of a unique diffraction line in a sample to that for a pure sample. Figure \(\PageIndex{2}\) for a mixture of calcite and magnesite (MgCO3) shows that a simultaneous quantitative analysis for both compounds is possible using the diffraction line at a \(2 \theta\) of 29.44 for calcite and of 32.65 for magnesite.
This page titled 12.4: Other X-Ray Methods was last modified on Wed, 28 Sep 2022 20:19:48 GMT and is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by David Harvey.
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