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Introduction to Health Physics: Fourth Edition - Ruang Baca FMIPA UB

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440 CHAPTER 9<br />

(b) The energy of the Comp<strong>to</strong>n electron (Comp<strong>to</strong>n edge) is equal <strong>to</strong> the difference<br />

between the energy of the incident pho<strong>to</strong>n and the scattered pho<strong>to</strong>n:<br />

E Comp<strong>to</strong>n electron = E − E ′ = 0.661 − 0.185 = 0.476 MeV.<br />

In pair production, a flicker of light representing the original quantum energy<br />

minus 1.02 MeV is produced as the positron and negatron simultaneously dissipate<br />

their energies in the crystal. After losing its energy, the positron combines with an<br />

electron, thus annihilating the two particles and producing two pho<strong>to</strong>ns of 0.51 MeV.<br />

Depending on the time sequence, the crystal size, and the geometric location of the<br />

initial interaction, we may have two pulses representing 0.51 MeV each—one light<br />

pulse representing 1.02 MeV, or one light pulse representing the <strong>to</strong>tal energy of the<br />

original pho<strong>to</strong>n.<br />

Nuclear Spectroscopy<br />

Nuclear spectroscopy is the analysis of radiation sources or radioiso<strong>to</strong>pes by measuring<br />

the energy distribution of the source. A spectrometer is an instrument that<br />

separates the output pulses from a detec<strong>to</strong>r, usually a scintillation detec<strong>to</strong>r or a<br />

semiconduc<strong>to</strong>r detec<strong>to</strong>r, according <strong>to</strong> size. Since the size distribution is proportional<br />

<strong>to</strong> the energy of the detected radiation, the output of the spectrometer<br />

provides detailed information that is useful in identifying unknown radioiso<strong>to</strong>pes<br />

and in counting one iso<strong>to</strong>pe in the presence of others. This technique has found<br />

widespread application in X-ray and gamma-ray analysis using NaI(TI) scintillation<br />

detec<strong>to</strong>rs and HPGe (high-purity germanium) semiconduc<strong>to</strong>r detec<strong>to</strong>rs, in beta<br />

analysis using liquid scintillation detec<strong>to</strong>rs or plastic scintillation detec<strong>to</strong>rs, and in<br />

alpha analysis using semiconduc<strong>to</strong>r detec<strong>to</strong>rs. Nuclear spectrometers are available<br />

in two types, either a single-channel instrument or a multichannel analyzer (MCA).<br />

The essentials of a single-channel spectrometer consist of the detec<strong>to</strong>r, a linear amplifier,<br />

a pulse-height selec<strong>to</strong>r, and a readout device, such as a scaler or a ratemeter<br />

(Fig. 9-10). The pulse height selec<strong>to</strong>r is an electronic “slit,” which may be adjusted<br />

<strong>to</strong> pass pulses whose amplitude lies between any two desired limits of maximum and<br />

minimum. The output from the pulse-height analyzer is a logic pulse <strong>to</strong> a scaler or <strong>to</strong><br />

a count ratemeter. The main use of the single-channel analyzer is <strong>to</strong> discriminate between<br />

a desired radiation and other radiations that may be considered noise. Thus,<br />

the single-channel spectrometer is used <strong>to</strong> measure one radiation in the presence<br />

of another or <strong>to</strong> optimize the signal-<strong>to</strong>-noise ratio when a low-activity source is being<br />

measured in the presence of a significant background.<br />

An MCA (Fig. 9-11) has an analog-<strong>to</strong>-digital converter (ADC) instead of a pulseheight<br />

selec<strong>to</strong>r <strong>to</strong> sort all the output pulses from the detec<strong>to</strong>r according <strong>to</strong> height.<br />

The MCA also has a computer memory for s<strong>to</strong>ring the information from the ADC<br />

or from another source. This feature allows au<strong>to</strong>mated data-processing operations<br />

such as background subtraction and spectrum stripping. Spectrum stripping is a<br />

technique for analysis of compound spectra that is based on sequential subtraction<br />

of known gamma-ray spectra of individual iso<strong>to</strong>pes from the compound spectrum

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