RESUMO
The second part of an intercomparison of the coincidence summing correction methods is presented. This exercise concerned three volume sources, filled with liquid radioactive solution. The same experimental spectra, decay scheme and photon emission intensities were used by all the participants. The results were expressed as coincidence summing corrective factors for several energies of (152)Eu and (134)Cs, and different source-to-detector distances. They are presented and discussed.
Assuntos
Algoritmos , Artefatos , Radioisótopos/análise , Radioisótopos/normas , Radiometria/métodos , Radiometria/normas , Espectrometria gama/métodos , Meia-Vida , Internacionalidade , Doses de Radiação , Radioisótopos/química , Padrões de Referência , Valores de ReferênciaRESUMO
In order to assure Quality Control in accordance with ISO/IEC 17025, it was important, from metrological point of view, to examine the long-term stability of calibration standards previously prepared. Comprehensive reconsideration on efficiency curves with respect to the ageing of calibration standards is presented in this paper. The calibration standards were re-used after a period of 5 years and analysis of the results showed discrepancies in efficiency values.
Assuntos
Calibragem/normas , Radioisótopos/análise , Radioisótopos/química , Radiometria/normas , Internacionalidade , Estudos Longitudinais , Doses de Radiação , Padrões de Referência , Valores de ReferênciaRESUMO
A simple and efficient method for determination of uranium content in surface soil samples contaminated with depleted uranium, by gamma ray spectrometry is presented. The content of natural uranium and depleted uranium, as well as the activity ratio (235)U/(238)U of depleted uranium, were determined in contaminated surface soil samples by application of this method.
Assuntos
Monitoramento de Radiação/métodos , Poluentes Radioativos do Solo/análise , Urânio/análise , Métodos , Espectrometria gama/métodosRESUMO
A review of the calibration procedures of the semiconductor HPGe spectrometer is presented in this paper. Calibration standards were prepared using the standardized radioactive solution of the common monoenergetic radionuclides mixture and standardized multigamma (152)Eu solution. The matrix materials were spiked using the activated carbon, and homogenized mechanically or by suspension in C(2)H(5)OH. Experimentally determined efficiency curves were compared with those obtained by Monte Carlo simulation.
RESUMO
A method for determining the specific alpha activity of thick sources using a large area ZnS(Ag) scintillation detector is presented. In this method a quadratic relationship between the detector response and window thickness is assumed. This method provides a quick estimation of alpha activity in the sample, so it is an indicative method. The aim of this experimental work is to approve theoretical assumption and to develop a standard routine method for absolute alpha measurements of thick contaminated environmental sources. For this purpose reference material U(3)O(8) and spiked standards of soil were used. Measurements of contaminated soil samples from south Serbia showed the practical application of this method.
Assuntos
Contagem de Cintilação/métodos , Poluentes Radioativos do Solo/análise , Partículas alfa , Óxidos/análise , Monitoramento de Radiação , Compostos de Tório/análise , Compostos de Urânio/análise , Iugoslávia , Compostos de ZincoRESUMO
The surface air activity concentration of 241Pu for the period May 01-15, 1986, for a monitoring site in Vinca, Belgrade was retrospectively estimated. The results were obtained by re-measurement of plutonium fraction alpha-spectrometric sources, with 236Pu as a tracer, used almost 13 years earlier for the determination of (239,240)Pu concentration in surface air immediately after the Chernobyl accident. The estimated 241Pu concentration, based on the 241Am in-growth method for air samples, ranged from 240 to 7800 microBq/m3. The average activity ratio 241Pu/(239,240)Pu originating from the Chernobyl accident at Belgrade site was approximately 100 at the collection time.