Plutonium Biokinetics in Human Body A. Luciani - Kit-Bibliothek - FZK
Plutonium Biokinetics in Human Body A. Luciani - Kit-Bibliothek - FZK
Plutonium Biokinetics in Human Body A. Luciani - Kit-Bibliothek - FZK
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This quantity is normally expressed as a percentage. The ma<strong>in</strong> important factors<br />
affect<strong>in</strong>g the energy resolution are:<br />
• the statistical fluctuations <strong>in</strong> the number of charge carriers (i.e. electron-hole pair)<br />
produced <strong>in</strong> the detector;<br />
• the electronic noise <strong>in</strong> the detector itself, the preamplifier and the amplifier;<br />
• the <strong>in</strong>complete collection of the charge carriers.<br />
Such factors are generally present <strong>in</strong> any k<strong>in</strong>d of detect<strong>in</strong>g system. For a sc<strong>in</strong>tillation<br />
detector further factors affect the energy resolution because the <strong>in</strong>itial electric sign is firstly<br />
converted <strong>in</strong>to light and then converted aga<strong>in</strong> <strong>in</strong>to an electric one. Such further factors are the<br />
emission of the lum<strong>in</strong>escence, the collection of photons on the photocathode and the emission<br />
of photoelectrons.<br />
The energy (w) spent by a radiation <strong>in</strong>teract<strong>in</strong>g with a detect<strong>in</strong>g materials to create one<br />
electron-hole pair (as <strong>in</strong> the semiconductor detectors) is actually greater than the energy gap<br />
(E g) between valence and conduction bands. For <strong>in</strong>stance for a Germanium detector the mean<br />
energy required for creat<strong>in</strong>g a pair is 2.96 eV whereas the energy gap is only about 0.67 eV at<br />
300 K. This difference between w and E g reveals that part of the energy is dissipated <strong>in</strong>to<br />
processes that don’t generate charge carriers. Therefore if the energy E is deposited <strong>in</strong> the<br />
detector, the average number of charge carriers is given by E/w and <strong>in</strong> case of a pure Poisson<br />
statistical process the standard deviation of the number of pairs should be just the square root<br />
of such ratio. Yet, the experience has shown that the fluctuations are smaller. A factor, called<br />
Fano factor (F), is therefore <strong>in</strong>troduced and the standard deviation of the number of charged<br />
carriers is more realistically given by:<br />
σ = FE<br />
w<br />
54<br />
equation 2.3.2<br />
The two extreme values of F are 0 and 1. The former means there are no statistical<br />
fluctuations and all the energy is spent for generat<strong>in</strong>g charged carriers. The latter means that<br />
the number of produced pairs is governed by Poisson statistics. If the distribution of an energy<br />
spectrum relat<strong>in</strong>g to a monoenergetic source with energy E is described with a Gaussian<br />
function, the FWHM results as follow<strong>in</strong>g [129]:<br />
FWHM = 2 2ln(2)w = 2 2ln(2)wFE<br />
equation 2.3.3<br />
It results that the FWHM and so the energy resolution decreases with decreas<strong>in</strong>g values of w.<br />
On the basis of such considerations a semiconductor detector is expected to have the<br />
best energy resolution, thanks to its low energy threshold for an electron-hole pair production.<br />
S<strong>in</strong>gle full energy peaks even separated by few keV energies can be easily identified <strong>in</strong> the<br />
spectrum. In case of sc<strong>in</strong>tillation detectors full energy peaks can be still located and the<br />
centroid calculated, but the lower energy resolution doesn’t allow sometimes to dist<strong>in</strong>guish<br />
photons with energy closer than some ten keV.<br />
When s<strong>in</strong>gle full energy peaks are present energy calibration is easily performed. The<br />
centroids of the full energy peaks are associated to the energy of the emitted radiations,<br />
known from the decay characteristics of the radionuclides. A fitt<strong>in</strong>g is normally performed<br />
us<strong>in</strong>g a polynomial function to calculate the energy value of each channel of the MCA. On the<br />
basis of the energy calibration the energy of any further full energy peak can be evaluated and<br />
the relative radionuclide identified.