In the decommissioning process of nuclear power plants, Ni-59, Ni-63 and Fe-55 present in radioactive waste are crucial radionuclides used as fundamental indicators in determining waste treatment methods. However, due to their low-energy emissions, the chemical separation of these two radionuclides is essential compared to others. Therefore, this study aims to evaluate the suitability of various pre-treatment methods for decommissioning waste materials by conducting characteristic assessments at each chemical separation stage. The goal is to find the most optimized pre-treatment method for the analysis of Ni-59, Ni-63 and Fe-55 in decommissioning waste. The comparative evaluation results confirm that the chemical separation procedures for Fe and Ni are very stable in terms of stepwise recovery rates and the removal of interfering radionuclides. However, decommissioning waste materials, which mainly consist of concrete, metals, etc., possess unique properties, and a significant portion may be low-radioactivity waste suitable for on-site disposal. Considering that the chemical behavior and reaction characteristics may vary at each chemical separation stage depending on the matrix properties of the materials, it is considered necessary to apply cascading chemical separation or develop and apply individual chemical separation methods. This should be done by verifying and validating their effectiveness on actual decommissioning waste materials.

According to the Nuclear Safety and Security Commission (NSSC) Notice No. 2021-26 “Delivery Regulations for the Low- and Intermediate Level Radioactive Waste (LILW)”, the activity of 3H, 14C, 55Fe, 58Co, 60Co, 59Ni, 63Ni, 90Sr, 94Nb, 99Tc, 129I, 137Cs, 144Ce, and gross alpha must be identified. Currently, the scaling factor of the dry active waste (DAW) for LILW is applied as an indirect evaluation method in Korea. The analyses are used the destructive methods and 55Fe, 60Co, 59Ni, 63Ni, 90Sr, 94Nb, 99Tc, and 137Cs, which are classified as nonvolatile nuclides, are separated through sequential separation and then measured by gamma detector, liquid scintillation counter (LSC), alpha/beta total counter (Gas Proportional Counter, GPC), and ICP-MS. We will introduce how to apply the existing nuclide separation method and improve the measurement method to supplement it.

As the decommissioning and decontamination (D&D) of nuclear power plants (NPPs) has actively proceeded worldwide, the management of radiation exposure of workers has become more critical. Radioactive aerosol is one of the main causes of worker exposure, contributing to internal exposure by inhalation. It occurs in the process of cutting radioactive metal structures or melting radioactive wastes during D&D, and its distribution varies according to decommissioning strategies and cutting methods. Among the dominant radionuclides in radioactive aerosols, Fe-55 is known to be the most abundant. Fe-55, which decays by electron capture, is classified as a difficult-to-measure (DTM) radionuclide because its emitted X-rays have too low energy to measure directly from outside of the container. Generally, for measuring DTM nuclides, the liquid scintillation counting (LSC) method and the scaling factor (SF) method are used. However, these methods are not suitable for continuous monitoring of the D&D workplace due to the necessity of sampling and additional analysis. The radiation measurement system that can directly measure the radionuclides collected at the aerosol filter could be more useful. In this study, as preliminary research on developing the radioactive aerosol monitoring system, we fabricated a gamma-ray spectrometer based on a NaI (Tl) scintillator and measured the energy spectrum of Fe-55. A beryllium window was applied to the scintillator for X-ray transmission, and the Fe-55 check source was directly attached to the scintillator assuming that the aerosol filter was equipped. 5.9 keV photopeak was clearly observed and the energy resolution was estimated as 44.10%. Also, the simultaneous measurement with Cs-137 was carried out and all the peaks were measured.

원자로의 해체 과정에서 발생되는 방사성 폐기물 내 존재하는 55Fe, 63Ni은 폐기물의 처리방법을 결정하는 데 있어 기초적인 지표로 활용되는 중요한 핵종이다. 하지만 두 핵종은 낮은 방사선량으로 인해 다른 핵종들과의 분리가 필수적이며 또한 시 료 매질에서 완전히 추출할 수 있는 전처리가 선행되어야 한다. 따라서 본 연구는 다양한 매질의 원자로 해체 폐기물에 대한 전처리방법의 적용성을 평가하기 위해 NIST SRM 5종 (1646a, 1944, 8704, 2709a, 1633c)에 대하여 왕수, 불산, 과염소산을 각각 이용하는 습식산화법과 alkali-fusion 전처리법에 따른 Iron와 Nickel의 회수율을 비교하였다. 실험 결과 alkali-fusion 방법은 다양한 매질의 인증표준물질에 대해 Iron 95.3~98.3%, Nickle 86.6~88.1%의 분석 정확도와 2% 이하의 정밀도를 나타냄으로서 해체폐기물 중 55Fe, 63Ni 분석에 가장 최적화된 전처리법으로 판단된다.

추출크로마토그래피법과 액체섬광계수법을 이용하여 고체 시료중의 와 방사능을 측정할 수 있는 분석법을 확립하고 연구로 2호기의 해체시 발생되는 방사화된 콘크리트 폐기물을 분석하였다. 침전법과 추출크로마토그래피법으로 화학분리를 하면, 경우 Fe의 화학적 회수율은 대부분의 시료에서 90%이상이었으나 Ni의 회수율은 43.6과 46.5%를 나타낸 시료가 있으며 나머지는 62% 이상을 나타내었다. Spiked 시료를 이용하여 분리과정과 액체섬광계수법의 과정을 확인한 결과 의 경우는 3.7% 오차내의, 의 경우는 0.7% 오차내의 결과가 얻어졌다. 연구로 2호기의 해체 콘크리트 시료중 방사능은 MDA이하의 값도 있으나 TC3시료의 경우는 362Bq/g의 값이 얻어졌다. 그리고 의 경우는 모든 시료에서 MDA이하 값이 얻어져 이 존재하지 않음을 알 수 있었다. 그리고 콘크리트 벽의 해체시 표면의 시료는 의 방사능이 높다가 표면으로부터 깊은 시료일수록 의 방사능이 급격히 줄어들었다.