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International Reactor Dosimetry File 2002 - IAEA Publications

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Burnup is defined as the nuclear transmutation of a given isotope, and the<br />

correction for the nuclear burnup of a stable target isotope is given by:<br />

where:<br />

B = [1 – exp(–sjt)] (II.4)<br />

B<br />

jt<br />

s<br />

t<br />

j<br />

is the burnup correction factor (i.e. the ratio of the measured reaction<br />

rate to the true reaction rate);<br />

is the neutron fluence for the irradiation;<br />

is the spectral averaged cross-section;<br />

is the irradiation time;<br />

is the total neutron flux.<br />

sj can be defined as the product of the activation cross-section and the<br />

neutron flux spectrum integrated over the entire neutron energy spectrum, and<br />

is also equal to the total activation rate in product atoms per target atoms per<br />

second that can be calculated from reactor dosimetry activation measurements.<br />

Prior to neutron spectral adjustment, measured activation data are converted<br />

to these saturated activation rates. Equation (II.4) may be applied in order to<br />

determine if a burnup correction may be required for a specific reaction.<br />

However, if the burnup is significant, the measured reaction rate will be much<br />

lower than the true reaction rate as implied in Eq. (II.4). Furthermore, the<br />

possibility of burnup of the product atoms has to be considered, which may well<br />

be at a higher rate than that of the target atoms. The more general form of the<br />

burnup equation (which also takes into account the decay of the product atom)<br />

is given by:<br />

where:<br />

B = l[exp(–s a jt) – exp(–s b jt)]/[(l + s b j – s a j)(1 – exp(–lt))] (II.5)<br />

B is the ratio of the measured reaction rate to the true reaction rate;<br />

s a and s b are the spectral averaged cross-sections for the target and product<br />

atom, respectively;<br />

l is the decay constant for the product isotope.<br />

As noted above, this equation requires that the true reaction rates be<br />

known, whereas only a measured reaction rate for the target reaction may be<br />

known. This problem can be easily solved by applying an iterative procedure.<br />

Given a measured and uncorrected reaction rate for the target isotope, the<br />

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