Recently, the spent fuel pools withdrawn from nuclear power plants in Korea have been saturated.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.

Radioactive contamination of soil on the site of a nuclear facility has a characteristic that radioactive nuclides are adsorbed into the pores between soil particles, making it quite difficult to decontaminate. For this reason, research on the development of various decontamination processes is being actively conducted. In this study, among various decontamination studies, a soil decontamination process using supercritical carbon dioxide was presented. The decontamination process uses supercritical carbon dioxide as the main solvent, which has a higher penetration power than other materials. Therefore, the process consists of the process of desorbing and extracting the target radionuclides between particles of soil. However, since nuclides exist as ions in the soil, polar chelating ligand material was introduced as an additive to nonpolar supercritical carbon dioxide for smooth chemical reactions in the soil. Thereafter, from the viewpoint of improving process continuity and efficiency, an alcohol material was introduced as an auxiliary solvent for liquefaction of chelating ligand in a solid state. Through prior research on the selection of a solvent for liquefaction of chelating ligand, ethanol and 2-propanol were finally selected based on whether the chelating ligand was dissolved. However, if the auxiliary solvent in which the chelating ligand is dissolved is to be combined with radionuclides in the soil, it must first be well dissolved in supercritical carbon dioxide, the main solvent. Therefore, in this study, the solubility of ethanol and 2-propanol in supercritical carbon dioxide was measured and the suitability was evaluated. The temperature conditions were carried out at 40°C, the same as the previously designed decontamination process, and the measurement was conducted by adjusting the pressure and volume through a syringe pump and a variable volume device. In addition, solubility was measured based on the observation of the ‘cloud point’ in which the image becomes cloudy and then bright. As a result of the experiment, several solubility points were measured at a pressure of 150 bar or less. If the flow rate ratio of supercritical carbon dioxide and auxiliary solvent derived from the results is applied to the soil decontamination process, it is expected that the process efficiency will increase in the future.

Korea faces decommissioning the nation’s first commercial nuclear power plant, the Kori-1 and Wolseong-1 reactors. In addition, other nuclear power plants that will continue to operate will also face decommissioning over time, so it is essential to develop independent nuclear facility decommissioning and site remediation technologies. Among these various technologies, soil decontamination is an essential not only in the site remediation after the decommissioning of the highly radioactive nuclear facility, but also in the case of site contamination caused by an accident during operation of the nuclear facility. But the soil, which is a porous material, is difficult to decontaminate because radionuclides are adsorbed into the pores. Therefore, with the current decontamination technology, it is difficult to achieve the two goals of high decontamination efficiency and secondary waste reduction at the same time. In this study, a soil decontamination process with supercritical carbon dioxide as the main solvent was presented, which has better permeability than other solvents and is easy to maintain critical conditions and change physical properties. Through prior research, a polar chelating ligand was introduced as an additive for smooth extraction reaction between radionuclides present as ions in soil and nonpolar supercritical carbon dioxide. In addition, for the purpose of continuity of the process, a candidate group of auxiliary solvents capable of liquefying the ligand was selected. In this research evaluated the decontamination efficiency by adding the selected auxiliary solvent candidates to the supercritical carbon dioxide decontamination process, and ethanol with the best characteristics was selected as the final auxiliary solvent. In addition, based on the decontamination effect under a single condition of the auxiliary solvent found in the Blank Test process, the possibility of a pre-treatment leaching process using alcohol was tested in addition to the decontamination process using supercritical carbon dioxide. Finally, in addition to the existing Cs and Sr, the possibility of decontamination process was tested by adding U nuclides as a source of contamination. As a result of this research, it is expected that by minimizing secondary waste after the process, waste treatment cost could be reduced and the environmental aspect could be contributed, and a virtuous cycle structure could be established through reuse of the separated carbon dioxide solvent. In addition, adding its own extraction capacity of ethanol used for liquefaction of solid-phase ligands is expected to maximize decontamination efficiency in the process of increasing the size of the process in the future.