Analytical Methods 101 – XRF

Principle of X-Ray Fluorescence. Translated after Matthias Ahlfeld www.weltderphysik.de

In our blog, we don’t only give you updates on our research but also give you a bit of an insight into our specialist disciplines.
This posting will be of interest to you if you are interested in analytical methods, because today we will have a brief look at X-ray fluorescence analysis. This method is usually used to determine the total chemistry of a sample and has the great advantage of being easily reproducible and correct.

X-ray fluorescence (XRF) is a non-destructive, quantitative, as well as qualitative analysis, which reflects the concentration of the elements of the sample, often display in weight percentage (wt%) and in the form of oxides. XRF can measure all the elements whose atomic number is greater than or equal to four, i.e. boron. The detection limit, the smallest measurable amount of an element, of this method ranges for 1 – 10 ppm, whereas ppm stands form “parts per million” and can also be expressed as 0,0001 % as a more understandable unit.

During the measurement, the atoms of a sample are bombarded with high-energy X-ray photons. If a photon hits an electron, it is shot out of its shell. The resulting gap is filled by electrons from energetically higher shells. By switching to an energetically lower level, energy in the form of fluorescent radiation, i.e. element-characteristic X-rays, is released and can be measured. This effect is also known as fluorescence.

To obtain analytical results, the sample must be homogenized in advance. This is done by crushing and grinding, whereby a particle size of < 100 µm is aimed for and in the best case is around 50 µm. After processing the sample material is pressed into pellets or fused and casted into glass disks.

Results are often displayed in form of a spreadsheet like you can see it in the picture below.

ReSoURCE_XRF Results

Figure 1 Preliminary XRF results of CRK 1

The here presented knowledge can be backed up by the following textbooks:

  • German: Amthauer, G. & Pavicevic, M. K. (2000). Mikroskopische, analytische und massenspektrometrische Methoden. Physikalisch-chemische Untersuchungsmethoden in den Geowissenschaften: Bd. 1. Schweizerbart. S. 115
  • English: Putnis, A. (1992). Introduction to mineral sciences. Cambridge University Press. P. 109

Featured image: Principle of X-Ray Fluorescence. Translated after Matthias Ahlfeld www.weltderphysik.de. (CC BY-NC-ND 3.0) Original: https://www.weltderphysik.de/gebiet/teilchen/licht/synchrotronstrahlung/roentgenfluoreszenzanalyse/roentgenfluoreszenzanalyse/ [accessed: 20230522]

Author’s Portrait

Florian Feucht

DI Florian Feucht, is research associate at the Chair of Waste Management and Waste Treatment at the Montanuniversitaet Leoben, and part of the Workgroup: “Environmental remediation and mineral waste”. Since 2023 he participates in the Montanuniversitaet’s PhD Program.

From 2018 to 2023 he studied “applied geoscience” at the Montanuniversitaet Leoben and wrote his master thesis about “Chemical-Mineralogical Characterization of Ladle Slag from voestalpine Linz”.

From 2014 to 2018 he studied at the University of Vienna Earth Sciences and wrote a bachelor thesis on the subject: “Petrological and Petrographical Ínvestigation of Mafic-, Ultramafic Rocks from the Dunkelsteinerwald, Gföhler Unit, Moldanubic”

Florian’s research interests are chemical-mineralogical characterisation of mineral wastes, Mineralogy, Slag mineralogy, Recycling and Waste Management.

ReSoURCE Florian Feucht - Montanuni Leoben

Florian Feucht

Author

Florian Feucht, is research associate at the Chair of Waste Management and Waste Treatment at the Montanuniversitaet Leoben.

florian.feucht@unileoben.ac.at

Partner