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CSEM Scientific and Technical Report 2008

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Element Sensitive X-ray Imaging – a Roentgen Progress<br />

J. Nüesch, P. Seitz<br />

X-ray absorption spectroscopy allows detecting the elemental composition of an investigated object.<br />

For the last hundred years x-ray absorption images gave only<br />

the density of the scanned sample. There is the possibility to<br />

use the fluorescent radiation of a sample surface to determine<br />

its composition. But the volumetric information gets lost with<br />

this approach as the fluorescent radiation is emitted in 4 π <strong>and</strong><br />

it only works for the surface<br />

Figure 1: A sample setup to image an object with this technique.<br />

From right to left: source, object, <strong>and</strong> spectrometer.<br />

The element sensitive detection is possible due to an effect in<br />

the photoabsorption. In general the x-ray absorption is<br />

described by the Beer-Lambert-Law<br />

66<br />

���� �� � � ��·� � � � � ��·�·�<br />

�<br />

The loss of intensity I loss is dependent on the thickness x,<br />

the density ρ, <strong>and</strong> the mass-absorption coefficient � � �.<br />

In the<br />

x-ray domain up to about 60 keV the photoabsorption is the<br />

dominate effect. The simplified formula for the<br />

photoabsorption is<br />

� ��<br />

�<br />

� �� In most models the exponents a <strong>and</strong> b are considered to be<br />

constants. But these exponents are dependent on the energy<br />

(E) respective to the atomic number (Z). This crossdependency<br />

permits the calculation of the elemental<br />

composition.<br />

Figure 2: The part of the periodic system with the elements<br />

detectable in the range of 10 – 20 keV. All these elements are in this<br />

domain completely in photoabsorption without an edge.<br />

In the photoabsorption there is an additional effect not<br />

included in this equation. At the energy of each electron shell<br />

the function � �� ��� has a step, called edge. This limits in a<br />

first step the detection to the elements highlighted in Figure 2.<br />

The absolute density of the object cannot be measured by one<br />

measurement. This limit only calculates a density length<br />

product<br />

���·�<br />

If some kind of tomography is used or if x is known for the<br />

geometry all densities can be calculated.<br />

Counts [s -1 ]<br />

40<br />

35<br />

30<br />

25<br />

20<br />

15<br />

10<br />

5<br />

0<br />

0 7.8 15.6 23.4 31.2 39 46.8 54.6<br />

Energy [keV]<br />

Figure 3: The outputs of an Amptek semiconductor spectrometer with<br />

different elements in a beam at 40 kVp acceleration voltage. The<br />

three pure plates have a thickness of 500 µm.<br />

For the calculation the equation of the photoabsorption can be<br />

rewritten as<br />

���� � ��� � ·� ��<br />

This equation can be solved in linear algebra<br />

�� ���� ·���� ����������<br />

The matrix B can be calculated with reference data.<br />

Afterwards the areal density is directly calculated from the<br />

measurements.<br />

The X-ray spectrometer from Amptek (Figure 1) used at the<br />

moment has a resolution up to 149 eV @ 5.9 keV. Besides the<br />

spectral resolution the number of the maximal counts per<br />

second is important (Figure 3). This limits the maximal<br />

intensity of the beam. Overshooting this limit will increase the<br />

error of the signal as double impact cannot be detected in all<br />

cases <strong>and</strong> some measures must be discarded.<br />

�<br />

Al<br />

Si<br />

Ti

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