Handheld XRF: How it works

When your business considers an XRF purchase, there are many details to consider and many questions that you may have. What is XRF? What does XRF do? What elements does it analyze? Is XRF accurate? Is it fast?

Whilst handheld XRF can be used by non-experts, with pre-programmed settings allowing positive materials identification, the detection of impurities in production materials or the screening of food for toxic heavy metals (and more), you may still be curious about what is happening behind the scenes in handheld XRF guns.

If you and your coworkers are asking yourselves these questions and want to know more, you will find some helpful answers below.

XRF is an acronym for X-ray fluorescence, a process whereby electrons are displaced from their atomic orbital positions, releasing a burst of energy characteristic of a specific element. This release of energy is then registered by the detector in the XRF instrument, which in turn categorizes the energies by element. Here is a detailed breakdown of the process:

• An X-ray beam with enough energy to impact the electrons in the inner shells of the atoms in a sample is created by an X-ray tube inside the handheld analyzer. The X-ray beam is then emitted from the front end of the handheld XRF analyzer.
• The X-ray beam then interacts with the atoms in the sample by displacing electrons from the inner orbital shells of the atom. This displacement occurs as a result of the difference in energy between the primary X-ray beam emitted from the analyzer and the binding energy that holds electrons in their proper orbits; the displacement happens when the X-ray beam energy is higher than the binding energy of the electrons with which it interacts. 
• Electrons are fixed at specific energies in their positions in an atom, and this determines their orbits. Additionally, the spacing between the orbital shells of an atom is unique to the atoms of each element, so an atom of potassium (K) has different spacing between its electron shells than an atom of gold (Au), or silver (Ag), etc.
• When electrons are knocked out of their orbit, they leave behind vacancies, making the atom unstable. The atom must immediately correct the instability by filling the vacancies that the displaced electrons left behind. Those vacancies can be filled from higher orbits that move down to a lower orbit where a vacancy exits. For example, if an electron is displaced from the innermost shell of the atom (the one closest to the nucleus), an electron from the next shell up can move down to fill the vacancy. This is fluorescence.
• When electrons are knocked out of their orbit, they leave behind vacancies, making the atom unstable. The atom must immediately correct the instability by filling the vacancies that the displaced electrons left behind. Those vacancies can be filled from higher orbits that move down to a lower orbit where a vacancy exits. For example, if an electron is displaced from the innermost shell of the atom (the one closest to the nucleus), an electron from the next shell up can move down to fill the vacancy. This is fluorescence.
• Electrons have higher binding energies the further they are from the nucleus of the atom. Therefore, an electron loses some energy when it drops from a higher electron shell to an electron shell closer to the nucleus. The amount of energy lost is equivalent to the difference in energy between the two electron shells, which is determined by the distance between them. The distance between the two orbital shells is unique to each element, as mentioned above.
• The energy lost can be used to identify the element from which it emanates, because the amount of energy lost in the fluorescence process is unique to each element. The individual fluorescent energies detected are specific to the elements that are present in the sample. In order to determine the quantity of each element present, the proportion in which the individual energies appear can be calculated by the instrument or by other software.

The entire fluorescence process occurs in small factions of a second.  A measurement using this process and a modern handheld XRF gun can be made in a matter of seconds.  The actual time required for a measurement will depend on the nature of the sample and the levels of interest.  High percentage levels will take a few seconds while part-per-million levels will take a few minutes.

Contact Bruker today to find out more about XRF applications or to schedule a free demonstration of our instruments at your worksite.

Handheld XRF Applications:

• Elemental Composition Analysis
• Screening with XRF
• Quantitative, Semi-Quantitative and Qualitative XRF Data
• Handheld XRF vs Nitric Acid