Calibration of a 7.6 cm x 7.6 cm (3 inch x 3 inch) Sodium Iodide Gamma Ray Spectrometer for Air Kerma Rate

• Published in: Radiation protection dosimetry 2001-01, Vol.94 (4), p.309-316
• Main Authors: Grasty, R.L., Walters, B.R.B., Hovgaard, J., LaMarre, J.R.
• Format: Article
• Language: English
• Subjects: Air; Applied radiobiology (equipment, dosimetry...); Background Radiation; Biological and medical sciences; Biological effects of radiation; Calibration; Fundamental and applied biological sciences. Psychology; Monte Carlo Method; Noble Gases; Radiation Monitoring - methods; Signal Processing, Computer-Assisted; Sodium Iodide; Spectrometry, Gamma; Tissues, organs and organisms biophysics
• ISSN: 0144-8420; 1742-3406
• DOI: 10.1093/oxfordjournals.rpd.a006504

An experimental procedure is described for converting a gamma ray spectral measurement from a 7.6 cm x 7.6 cm (3 inch x 3 inch) sodium iodide (NaI) detector to air kerma rate. The calibration procedure involves measuring the energy deposited in the detector using 10 radioactive sources of known activity covering an energy range from 60 keV to 1836 keV. For each of the 10 sources, gamma ray spectra were measured with the source at different angles to the detector axis. The total energy deposited in the detector for the ten sources was confirmed by Monte Carlo calculations. The spectra measured at different angles were combined to produce a spectrum that would represent a homogeneous semi-infinite source of radiation. The resultant spectrum was then subdivided into 10 energy regions. Based on the known air kerma rates due to the sources, a calibration coefficient was calculated for each of the 10 energy regions. These calibration coefficients could then be used to convert the energy deposited in the 10 regions of an unknown spectrum to air kerma rate. The calibration procedure was confirmed by comparing the results from the detector with those from calibrated collimated beams of 137Cs and 60Co. A comparison of measurements using a calibrated pressurised ionisation chamber with those from a similar NaI spectrometer in Finland provided additional confirmation of the calibration procedure.