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Nuclear Spectroscopy

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mentally from a measurement of the counting rate of<br />

a source with known activity (a calibrated standard),<br />

or from an interpolation between measurements of<br />

calibrated sources at energies bracketing those being<br />

studied. For the 3.8 cm x 2.5 cm NaI(Tl) detector, the<br />

effective detector efficiency (πr 2 ε/4πd 2 ) as a function<br />

of gamma energy is shown in Figure 10.1.<br />

The source distance used for the data in Figure 10.1<br />

is the distance from the detector face to a commercially<br />

encapsulated source placed on the eighth shelf.<br />

Obtaining ε requires the knowledge of the solid<br />

angle, Ω/4π,<br />

2<br />

Ω πr<br />

10.2 =<br />

2<br />

4π<br />

4πd<br />

For source to detector distances that are much larger<br />

than the largest dimension of the detector, this Ω/4π<br />

calculation is straight forward. The shelf eight position<br />

is not far enough from the detector to meet this<br />

requirement. Calculations suggest that Ω/4π is about<br />

1.54 x 10 -2 . See the 1977 paper by E. M. Wray.<br />

Another technique for determining the absolute activity<br />

of a few special sources, such as 22 Na and 60 Co, is<br />

to utilize the sum peak in the detector spectrum,<br />

shown in Figure 1.1 for 22 Na. This peak occurs when<br />

two gammas arrive at the detector at about the same<br />

time (within the resolving time of the detection system).<br />

The pulses produced by each gamma interacting<br />

with the crystal combine to produce an event that<br />

the computer interprets as a gamma energy equal to<br />

the sum of the energies of the individual gammas,<br />

hence the name “sum” peak. The measured activity of<br />

the sum peak, A sum<br />

, depends upon the product of the<br />

absolute activity of the source and the individual<br />

probabilities for detecting each gamma, resulting in<br />

10.3<br />

A A r 2<br />

2<br />

π<br />

=<br />

d f π<br />

ε<br />

rd f<br />

2 γ B 2<br />

4π<br />

4π<br />

sum B γ A A<br />

In equation 10.3 the subscripts A and B refer to the<br />

two gammas that are coincident in the detector. For<br />

an isotope like 22 Na, one of the annihilation gammas<br />

(511 keV) and the 1,274 keV gamma from the nuclear<br />

state transition can be naturally coincident with each<br />

ε<br />

Effective Detection Efficiency<br />

0.01<br />

0.001<br />

J J<br />

J J<br />

J<br />

Figure 10.1 NaI(Tl) detector efficiency curve for a 3.8 cm x<br />

2.5 cm cylindrical crystal with a source on the eighth shelf.<br />

Larger crystals will have greater detection efficiencies. The<br />

effective detector efficiency is the product (πr 2 ε/4πd 2 ).<br />

J<br />

J<br />

J<br />

J<br />

J J J<br />

0.0001<br />

100 1000 4000<br />

Gamma Energy (keV)<br />

J<br />

Data<br />

linear fit<br />

other to form a sum peak. The reason they are<br />

coincident can be seen from the 22 Na decay scheme in<br />

Appendix D. In the decay of a single 22 Na nucleus, the<br />

1,274 keV gamma and the positron are emitted within<br />

picoseconds of each other. The positron annihilation<br />

occurs quickly after its emission, producing two<br />

oppositely-directed, 511 keV gammas. The direction<br />

of the 1,274 keV gamma emission is not correlated<br />

with the direction of emission of either 511 keV<br />

gamma. This results in a small probability that one<br />

511 keV gamma and the 1,274 keV gamma will arrive<br />

at the detector at the same time, due to the detector’s<br />

geometry. This probability is expressed as the product<br />

of the individual probabilities for the detection of<br />

each gamma, included in equation 10.3.<br />

Using equation 10.1 for the A and the B gammas to<br />

get A A<br />

and A B<br />

, you can obtain the absolute activity of<br />

the source, A, from equation 10.3 as<br />

10.4<br />

A<br />

AA A<br />

=<br />

A<br />

sum<br />

B<br />

This will work for sources where two gammas are<br />

emitted within the resolving time of the detector and<br />

there is no correlated direction between the two<br />

29

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