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        검색결과 1

        1.
        2023.05 구독 인증기관·개인회원 무료
        As a result of various generation, transmutation, and decay schemes, a wide variety of radionuclides exist in the reactor prior to accident occurrence. Considering all of the radionuclides as the accident source term in an offsite consequence analysis will inevitably take up excessive computer resources and time. Calculation time can be reduced with minimal impact on the accuracy of the results by considering only the nuclides that have a significant effect on the calculation among the potential radioactive sources that may be released into the environment. In earlier studies related to offsite consequence analysis, it is shown that the principal criteria for the radionuclide screening applied are as follows; radionuclide inventory in the reactor, radioactive half-life, radionuclide release fraction to the environment, relative dose contribution of nuclides within a specific group, and radiobiological importance. As a result, it is confirmed that 54, 60, and 69 nuclides are applied to the risk assessment performed in WASH-1400, NUREG-1150, and SOARCA (State-of-the-Art Reactor Consequence Analyses) project in the United States, respectively. In addition, in this study, the technical consultations with domestic and foreign experts were carried out to confirm details on criteria and process for screening out radionuclides in offsite consequence analysis. In this paper, based on the literature survey and technical consulting, we derived the screening process of selecting a list of radionuclides to be considered in the offsite consequence analysis. The first step is to eliminate radionuclides with little core inventory (less than specific threshold) or very short half-lives. However, important decay products of radionuclides that have short half-lives should not be excluded by this process. The next step is to further eliminate radionuclides by considering contribution to offsite impact, which is defined as a product of radioactivity released to the environment (i.e. ‘inventory in the reactor’ times ‘release fraction to offsite’) and comprehensive dose (or risk) coefficient taking into account all exposure pathways to be included. The final step is to delete isotopes that contribute less than certain threshold to any important dose metric through additional computer runs for each important source term. Even though it is presumed that this process is applicable to existing light water reactors and the set of accidents that would be considered in PSA, some of the assumptions or specific recommendations may need to be reconsidered for other reactor types or set of accident categories.