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1.
Health Phys ; 112(3): 276-281, 2017 03.
Article En | MEDLINE | ID: mdl-28121728

For Cs and Co gamma ray spectra, gamma ray energy is proportional to the amplitude of the pulse signal, and energy resolution can be improved by pulse signal processing with mathematical algorithms. Influenced by system measurement noise and baseline fluctuation, the pulse amplitude is difficult to calculate accurately. A method that combines the Kalman filter baseline estimation with the non-linear exponential fitting has been used. By this method, the pulse signal is divided into two parts: one is the raising edge before the pulse peak, and another is after the pulse peak. The pulse amplitude equals the difference between the pulse starting height and the pulse peak height. The pulse starting height is obtained by Kalman filter baseline estimation on the rising edge of the pulse starting point. The pulse peak height is calculated by nonlinear exponential fitting on the falling edge of the pulse highest point. When the sampling rate is 100 MHz, the pulse signals obtained from a Cd(Zn)Te detector are analyzed by this method. Results have shown that the processed pulses have a more distinguishable amplitude distribution; energy resolution for the Cs spectrum is approximately 2.97% at 662 keV (~19.66 keV FWHM), and for the Co spectrum it is 2.61% at 1,332 keV (~34.76 keV FWHM).


Algorithms , Cesium Radioisotopes/analysis , Copper Radioisotopes/analysis , Gamma Rays , Models, Statistical , Signal Processing, Computer-Assisted , Computer Simulation , Nonlinear Dynamics , Numerical Analysis, Computer-Assisted , Reproducibility of Results , Sensitivity and Specificity , Spectrometry, Gamma
2.
Health Phys ; 111(1): 17-21, 2016 07.
Article En | MEDLINE | ID: mdl-27218290

Delayed gamma spectrum is the fingerprint of uranium materials in arms control verification technology. The decay chain is simplified into basic state linear chain and excitation state linear chain to calculate and analyze the delayed gamma spectra of fission products. Formulas of the changing rule for nuclide number before and after zero-time are deduced. The C program for calculating the delayed gamma ray spectra data is constructed, and related experiments are conducted to verify this theory. Through analysis of the delayed gamma counts of several nuclides, the calculated results are found to be consistent with experimental values.


Algorithms , Materials Testing/methods , Nuclear Fission , Radiometry/methods , Software , Uranium/analysis , Uranium/chemistry , Half-Life , Reproducibility of Results , Sensitivity and Specificity , Uranium/radiation effects
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