To address the pressing societal concern in Korea, characterized by the imminent saturation of spent nuclear fuel storage, this study was undertaken to validate the fundamental reprocessing process capable of substantially mitigating the accumulation of spent nuclear fuel. Reprocessing is divided into dry processing (pyro-processing) and wet reprocessing (PUREX). Within this context, the primary focus of this research is to elucidate the foundational principles of PUREX (Plutonium Uranium Redox Extraction). Specifically, the central objective is to elucidate the interaction between uranium (U) and plutonium (Pu) utilizing an organic phase consisting of tributyl phosphate (TBP) and dodecane. The objective was to comprehensively understand the role of HNO3 in the PUREX (Plutonium Uranium Redox Extraction) process by subjecting organic phases mixed with TBPdodecane to various HNO3 concentrations (0.1 M, 1.0 M, 5.0 M). Subsequently, the introduction of Strontium (Sr-85) and Europium (Eu-152) stock solutions was carried out to simulate the presence of fission products typically contented in the spent nuclear fuel. When the operation proceeds, the complex structure takes the following form. 􀜷􀜱􀬶 􀬶􀬾(􀜽􀝍) + 2􀜰􀜱􀬷 􀬿(􀜽􀝍) + 2􀜶􀜤􀜲(􀝋􀝎􀝃) ↔ 􀜷􀜱􀬶(􀜰􀜱􀬷)􀬶 ∙ 2􀜶􀜤􀜲(􀝋􀝎􀝃) Subsequently, separate samples were gathered from both the organic and aqueous phases for the quantification of gamma-rays and alpha particles. Alpha particle measurements were conducted utilizing the Liquid Scintillation Counter (LSC) system, while gamma-ray measurements were carried out using the High-Purity Germanium Detector (HPGe). The distribution ratio for U, Eu (Eu-152), and Sr (Sr-84) was ascertained by quantifying their activity through LSC and HPGe. Through the experiments conducted within this program, we have gained a comprehensive understanding of the selective solvent extraction of actinides. Specifically, uranium has been effectively separated from the aqueous phase into the organic phase using a combination of tributyl phosphate (TBP) and dodecane. Subsequently, samples containing U(VI), Eu(III), and Sr(II) underwent thorough analysis utilizing LSC and HPGe detectors. Our radiation measurements have firmly established that the concentration of nitric acid enhances the selective separation of uranium within the process.

Spent fuels (SFs) are stored in a storage pool after discharge from nuclear power plants. They can be transferred to for the further processes such as dry storage sites, processing plants, or disposal sites. One of important measures of SF is the burnup. Since the radioactivity of SF is strongly dependent on its burnup, the burnup of SF should be well estimated for the safe management, storage, and final disposal. Published papers about the methodology for the burnup estimation from the known activities of important radioactive sources are somewhat rare. In this study, we analyzed the dependency of the burnup on the important radiation source activities using ORIGEN-ARP, and suggested simple correlations that relate the burnup and the important source activities directly. A burnup estimation equation is suggested for PWR fuels relating burnup with total neutron source intensity (TNSI), initial enrichment, and cooling time. And three burnup estimation equations for major gamma sources, 137Cs, 134Cs, and 154Eu are also suggested.

Recently, the spent fuel pools withdrawn from nuclear power plants in Korea have been saturated. Therefore, specific regulations on the management of spent fuel pools, such as transportation and intermediate storage are needed. The burnup history is directly related to the management of spent nuclear fuel. This is because the decision to handle nuclear fuel may vary depending on the initial concentration of nuclear fuel, the degree to which nuclear fuel is irradiated and radioisotope nuclides are decayed, and the cooling state in the spent nuclear fuel storage tank. The purpose of this study is to determine the burnup of fuel based on the value obtained by scanning the surface of spent nuclear fuel through a neutron detector. Conversely, a database of neutron signals that scan bundles of spent nuclear fuel with an instrument with an already identified combustion history needs to be completed. First of all, the correlation between burnup history and nuclides was identified in previous studies. By setting the burnup history as the input value in the ORIGEN-ARP code, it was possible to identify the radioactive isotopes remaining in the bundle of nuclear fuel. Neutrons can finally be measured based on the amount of nuclide inventory that constitutes spent nuclear fuel. Through MCNP, the neutron detector was simulated and signals were measured to confirm how it correlates with the previously acquired burnup history database. In addition, the M (sub-critical multiplication) value, which is essential for neutron measurement, was checked to confirm the degree to which additional neutrons were generated in spent nuclear fuel in a subcritical state. The target nuclear fuel assembly was CE16×16, WH14×14, and WH17×17, which confirmed the correlation (1) between burnup, enrichment, and cooling time with the previous research topic, TNSI (Total neutron source intensity). 􀜤􀜷􁈺􀜩􀜹􀝀/􀜯􀜶􀜷􁈻 = 0.83􁈺􀜵􀯇􁈻􀬴.􀬶􀬷􀬼 ∙ 􁈺􀜫􀜧􁈻􀬴.􀬸􀬺􀬶􀬻 ∙ 􀝁􀬴.􀬴􀬴􀬼􀬷∙􀯧 􁈺1􁈻 A neutron signal will be obtained from the case according to each burnup history constituting this database. In particular, PAR=SF, a function that calculates the production amount of the fission product, was used. To confirm the computational logic of SF, it was confirmed whether a reasonable calculation was made by calculating with a nuclide spectrum.

The management before disposal of spent nuclear fuel is an essential process for safe management. It is important to determine the amount of nuclide inventory in order to ensure the integrity of spent nuclear fuel, as radiation generated from the nuclides is generated along with residual heat in the spent nuclear fuel. Based on the data on the characteristics of spent nuclear fuel generated in Korea, the correlation equation between burnup and enrichment was derived by referring to overseas cases (Sweden). Source term analysis was performed using the SCALE ORIGEN ARP code by securing the burnup history of nuclear fuel. Calculation was performed by inputting the combustion history of the fuel WH14×14 and WH17×17 as a reference for CE16×16 spent fuel. Through this study, the relationship was identified using the burnup, enrichment, and cooling time factors that influence the characteristics of spent nuclear fuel. In addition, the total source and spectrum data from neutrons and gamma sources were used to find out the characteristics of fuel.

As the number of nuclear power plants whose design life has expired worldwide increases, the attempts are continuing to complete the project of nuclear back-end cycle, the last task of the nuclear industry. Decontamination is essential in the process of dismantling nuclear facilities and restoration sites to remove all or some of the regulatory controls from an authorized facility. Among radioactive wastes, particularly contaminated soil is characterized by difficult physical decontamination because radionuclides are adsorbed between soil particles, that is, pores. Therefore, chemical decontamination is mainly used, which has the disadvantage of generating a lot of secondary waste. In order to overcome these disadvantages, an eco-friendly soil decontamination process is being developed that can drastically reduce the amount of secondary waste generated by using supercritical carbon dioxide. Supercritical carbon dioxide can easily control its physical properties and has both liquid and gas properties. However, since supercritical carbon dioxide is non-polar, additives are needed to extract polar metal ions, which are the goal of decontamination. Therefore, ligand with both CO2-philic and metal binding regions was selected. In previous studies, the decontamination efficiency of soil was evaluated by reacting contaminated soil with solid ligand and co-ligand at once. When solid ligands were used, the decontamination efficiency was lower than expected, which was expected because chemical substances were somewhat difficult to exchange in the closed process. In this study, in order to increase the efficiency of the decontamination process, the need for a process of liquefying ligand and continuously flowing it has been raised. Therefore, a co-solvent that dissolves well at the same time in SCCO2, ligand, and co-ligand was selected. In the selection process, a total of eight substances were selected by dividing into six polar substances and two non-polar substances through various criteria such as economic feasibility, eco-friendliness, and harmlessness. Thereafter, ethanol was finally selected through solubility evaluation for SCCO2 and additives. It is expected that a more effective decontamination process can be constructed when the additive is liquefied using a solvent selected from the results of this study.

Today, the domestic and international nuclear power industry is experiencing an acceleration in the scale of the nuclear facility decommissioning market. This phenomenon is also due to policy changes in some countries, but the main reason is the rapid increase in the proportion of old nuclear power plants in the world, mainly in countries that introduced nuclear power plants in the early stages. Decontamination is essential in the process of decommissioning nuclear facilities. Among various decontamination targets, radionuclides are adsorbed between pores in the soil, making physical decontamination quite difficult. Therefore, various chemical decontamination technologies are used for contaminated soil decontamination, and the current decontamination technologies have a problem of generating a large amount of secondary wastes. In this study, soil decontamination technology using supercritical carbon dioxide is proposed and aimed to make it into a process. This technology applies cleaning technology using supercritical fluids to decontamination of radioactive waste, it has important technical characteristics that do not fundamentally generate secondary wastes during radioactive waste treatment. Supercritical carbon dioxide is harmless and is a very useful fluid with advantages such as high dissolution, high diffusion coefficient, and low surface tension. However, since carbon dioxide, a non-polar material, shows limitations in removing polar and ionic metal wastes, a chelating ligand was introduced as an additive. In this study, a ligand material that can be dissolved in supercritical carbon dioxide and has high binding ability with polar metal ions was selected. In addition, in order to increase the decontamination efficiency, an experiment was conducted by adding an auxiliary ligand material and ultrasonic waves as additives. In this study, the possibility of liquefaction of chelating ligands and auxiliary ligands was tested for process continuity and efficiency, and the decontamination efficiency was compared by applying it to the actual soil classified according to the particle size. The decontamination efficiency was derived by measuring the concentration of target nuclides in the soil before and after decontamination through ICP-MS. As a result of the experiment, it was confirmed that the liquefaction of the additive had a positive effect on the decontamination efficiency, and a difference in the decontamination efficiency was confirmed according to the actual particle size of the soil. Through this study, it is expected that economic value can be created in addition to the social value of the technology by ensuring the continuity of the decontamination process using supercritical carbon dioxide.