Thesis (M. Phil.)--University of Hong Kong, 2010. / Includes bibliographical references (leaves 139-[147]). Also available in print.

Thesis (M. Phil.)--University of Hong Kong, 2010. / Includes bibliographical references (leaves 139-[147]). Also available online.

In this study, two methods of analysing activity concentrations of natural radionuclides (U, Th and K) in soil are critically compared. These are the Window Analysis (WA) and Full Spectrum Analysis (FSA). In the usual WA method, the activity concentrations are determined from the net counts of the windows set around individual &gamma / -ray peaks associated with the decay of U, Th and K. In the FSA method, the full energy spectrum is considered and the measured spectrum is described as the sum of the three standard spectra (associated with U, Th and K, respectively), each multiplied by an unknown concentration. The concentrations are determined from the FSA and correspond to the activity concentrations of U, Th and K in the soil. The standard spectra derived from separate calibration measurements using the HPGe detector, represents the response of the HPGe to a Marinelli sample beaker containing an activity concentration of 1 Bq/kg.

published_or_final_version / Physics / Master / Master of Philosophy

In this study, two methods of analysing activity concentrations of natural radionuclides (U, Th and K) in soil are critically compared. These are the Window Analysis (WA) and Full Spectrum Analysis (FSA). In the usual WA method, the activity concentrations are determined from the net counts of the windows set around individual &gamma / -ray peaks associated with the decay of U, Th and K. In the FSA method, the full energy spectrum is considered and the measured spectrum is described as the sum of the three standard spectra (associated with U, Th and K, respectively), each multiplied by an unknown concentration. The concentrations are determined from the FSA and correspond to the activity concentrations of U, Th and K in the soil. The standard spectra derived from separate calibration measurements using the HPGe detector, represents the response of the HPGe to a Marinelli sample beaker containing an activity concentration of 1 Bq/kg.