Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
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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http://dx.doi.org/10.13075/mp.5893.2013.0055 | DOI Listing |
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