MEASUREMENT OF PERSONAL DOSE EQUIVALENT OF X AND GAMMA RADIATION BY RING DOSIMETER: RESULTS OF INTERCOMPARISON MEASUREMENTS

被引:0
|
作者
Adamowicz, Malgorzata [1 ]
Papierz, Sylwia [1 ]
Kacprzyk, Janusz [1 ]
Kaminski, Zbigniew [1 ]
Zmyslony, Marek [1 ]
机构
[1] Nofer Inst Occupat Med, Dept Radiat Protect, PL-91348 Lodz, Poland
关键词
interlaboratory comparisons; X-ray and gamma radiation; personal dose equivalent; ring dosimeter; thermoluminescence detectors;
D O I
暂无
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
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 H-p(0.07). In addition, calibration procedures used in dosimetric measurements in persons occupationally exposed to ionizing photon radiation X and gamma 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 gamma 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 ofinterlaboratory 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 H-p(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 H-p(0.07). The result of the comparison was satisfactory, therefore the correctness of the testing procedure was confirmed.
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页码:631 / 637
页数:7
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