ORIGINAL PAPER
Measurement of personal dose equivalent of X and gamma radiation by ring dosimeter: Results of intercomparison measurements
 
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Instytut Medycyny Pracy im. prof. J. Nofera / Nofer Institute of Occupational Medicine, Łódź, Poland (Zakład Ochrony Radiologicznej / Department of Radiation Protection)
 
 
Corresponding author
Małgorzata Adamowicz   

Zakład Ochrony Radiologicznej, Instytut Medycyny Pracy im. prof. J. Nofera w Łodzi, ul. św. Teresy 8, 91-348 Łódź
 
 
Med Pr Work Health Saf. 2013;64(5):631-7
 
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ABSTRACT
Background: The aim of the study was to present the results of the interlaboratory comparisons for ring dosimeters and to confirm that the applied method is suitable for measuring the personal dose equivalent HP(0.07). In addition, calibration procedures used in dosimetric measurements in persons occupationally exposed to ionizing photon radiation X and γ were presented. Materials and Methods: Ring dosimeters made of flexible plastics with the diameter of approximately 20 mm, equipped with two thermoluminescence (TL) detectors type MTS-N, were the subject of interlaboratory comparisons. Irradiated detectors were red out using a new manual TLD's reader (FIMEL, France). All TLD exposures were done for validation of TLD readers and were performed using the reference X-ray and γ beams with the ISO rod phantom. The methodology of performed exposures corresponded with the methods applied by the European Radiation Dosimetry Group (EURADOS), the European organizer of interlaboratory comparisons. Results: The energy, dose and angular characteristics of the ring dosimeter allowed to elaborate the formula for estimating and verifying the personal dose equivalent HP(0.07). The test was performed to check and confirm the correctness of the estimated characteristics. The test results were satisfactory, and thus the readiness to implement TLD reader in the used method and to participate in interlaboratory comparisons was confirmed. Conclusions: According to the requirements of the Polish Centre for Accreditation, the laboratory was participating in the interlaboratory comparison organized by EURADOS in terms of the personal dose equivalent HP(0.07). The result of the comparison was satisfactory, therefore the correctness of the testing procedure was confirmed. Med Pr 2013;64(5):631–637
eISSN:2353-1339
ISSN:0465-5893
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