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True Coincidence Summing Correction in Gamma Spectroscopy

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For environmental measurement that <strong>in</strong>volve a limited set of radionuclides, it would<br />

be better to make the measurements relative to a reference standard for each nuclide<br />

rather than depend<strong>in</strong>g on upon <strong>in</strong>terpolation of a calibration curve. This <strong>in</strong>terpolation<br />

<strong>in</strong>troduces extra uncerta<strong>in</strong>ties added to those <strong>in</strong>volved <strong>in</strong> produc<strong>in</strong>g a po<strong>in</strong>t on the<br />

curve. Due to the above mentioned factors, the calibration curve may not be<br />

accurate. If the spectrum analysis program requires a calibration curve, then a curve<br />

must be created. However, the follow<strong>in</strong>g correction factors should be considered <strong>in</strong><br />

us<strong>in</strong>g calibration curves;<br />

Figure-1.9 Full peak energy calibration curve for a Mar<strong>in</strong>elli Beaker<br />

i. Dead-time correction<br />

The dead-time correction factor is (1-Rτ) -1 , where τ is the dead-time value<br />

selected for the dead-time module and R is the total count rate above the<br />

threshold <strong>in</strong>clud<strong>in</strong>g the digital overflows. Such factor depends on the sample’s<br />

count rate.<br />

ii.<br />

Pile-up correction<br />

A pulse will be counted and stored whenever it is not followed or preceded by<br />

another pulse dur<strong>in</strong>g a certa<strong>in</strong> period of time τ, the resolution time of the electronic<br />

system. Us<strong>in</strong>g the Poisson distribution, the probability of a random co<strong>in</strong>cidence,<br />

p c , with<strong>in</strong> τ is;<br />

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