When damaged nuclear fuel is stripped and re-fabricated into stabilized pellets, it is necessary to analyze the characteristics of the stabilized pellets, such as density, leaching behavior, and compressive strength, for final disposal. In this study, simulated nuclear fuel with UO2 and burn-up of 35 GWd/tU and 55 GWd/tU was used to measure the compressive strength of the stabilization pellet. In order to change the density of the sintered pellet, a sintered pellet was prepared by heat treatment at 1,550°C and 1,700°C for 6 hours in a reducing atmosphere of 4% H2/Ar. In the case of UO2, the density was 10.4 g/cm3 (94.5% of T.D.) and 10.6 g/cm3 (96.6% of T.D.) depending on the sintering temperature (1,550°C, 1,700°C). In the case of simulated fuel with a burn-up of 35 GWd/tU, the density was 8.8 g/cm3 (80.9% of T.D.) and 10.2 g/cm3 (93.6% of T.D.) depending on the sintering temperature (1,550°C, 1,700°C). In the case of simulated fuel with a burn-up of 55 GWd/tU, the density was 8.3 g/cm3 (77.0% of T.D.) and 10.0 g/cm3 (92.3% of T.D.) depending on the sintering temperature (1,550°C, 1,700°C). It was found that the compressive strength of simulated nuclear fuel decreased with increasing burn-up and increased with increasing density. In the case of UO2, the compressive strengths were 717.8 MPa and 897.4 MPa when the densities were 10.4 g/cm3 and 10.6 g.cm3, respectively. In the case of simulated nuclear fuel with a burn-up of 35 GWd/tU, the compressive strengths were 472.1 MPa and 732.3 MPa when the densities were 8.8 g/cm3 and 10.2 g/cm3. In the case of simulated nuclear fuel with a burn-up of 55 GWd/tU, the compressive strengths were 301.4 MPa and 515.5 MPa when the densities were 8.3 g/cm3 and 10.0 g/cm3, respectively.

Separating nuclides from spent nuclear fuel is crucial to reduce the final disposal area. The use of molten salt offers a potential method for nuclide separation without requiring electricity, similar to the oxide reduction process in pyroprocessing. In this study, a molten salt leaching technique was evaluated for its ability to separate nuclides from simulated oxide fuel in MgCl2 molten salts at 800°C. The simulated oxide fuel contained 2wt% Sr, 3wt% Ba, 2wt% Ce, 3wt% Nd, 3wt% Zr, 2wt% Mo, and 89wt% U. The separation of Sr from the simulated oxide fuel was achieved by loading it into a porous alumina basket and immersing it in the molten salt. The concentration of Sr in the salt was measured using ICP analysis after sampling the salt outside the basket with a dip-stick technique. The separated nuclides were analyzed with ICP-OES up to a duration of 156 hours. The results indicate that Ba and Sr can be successfully separated from the simulated fuel in MgCl2, while Ce, Nd, and U were not effectively separated.

In Korea, borated stainless steel (BSS) is used as spent fuel pool (SFP) storage rack to maintain nuclear criticality of spent fuels. As number of nuclear power plants and corresponding number of spent fuels increased, density in SFP storage rack also increased. In this regard, maintain subcriticality of spent nuclear fuels was raised as an issue and BSS was selected as structural material and neutron absorber for high density storage rack. Because it is difficult to replace storage rack, corrosion resistance and neutron absorbency are required for long period. BSS is based on stainless steel 304 and it is specified in the ASTM A887-89 standard depending on the boron concentration from 304B (0.20-0.29% B) to 304B7 (1.75-2.25% B). Due to low solubility of boron in austenitic stainless steel, metallic borides such as (Fe, Cr)2B are formed as secondary phase metallic borides could make Cr depletion near it which could decrease the corrosion resistance of material. In this paper, long-term corrosion behavior of BSS and its oxide microstructures are investigated through accelerated corrosion experiment in simulated SFP condition. Because corrosion rate of austenitic stainless steel is known to be dependent on the Arrhenius equation, a function of temperature, corrosion experiment is conducted by increasing the experimental temperature. Detail microstructural analysis was conducted with scanning electron microscope, transmission electron microscope and energy dispersive spectrometer. After oxidation, hematite structure oxide film is formed and pitting corrosions occur on the surface of specimens. Most of pitting corrosions are found at the substrate surface because corrosion resistance of substrate, which has low Cr content, is relatively low. Also, oxidation reaction of B in the secondary phase has the lowest Gibbs free energy compared to other elements. Furthermore, oxidation of Cr has low Gibbs free energy which means that oxidation of B and Cr could be faster than other elements. Thus, the long-term corrosion might affect to boron content and the neutron absorption ability of the material.

Separation of high heat generating-radioactive isotopes from spent nuclear fuel is an important issue because it can reduce the final disposal area. As one of the technologies that can selectively separate only high heat generating-radioactive isotopes without dissolving spent fuel, the methods using molten salt have recently attracted attention. Although studies on chemical changes of Sr oxides in molten salts have been reported, they have limitation in that alternative oxide reagents rather than oxide fuel were used. In this study, the separation behaviors of Sr from simulated oxide fuel using various molten salts were investigated. A powder type containing 95.7wt% of U and 0.123wt% of Sr was used as the simulated oxide fuel. LiCl, LiCl-CaCl2, MgCl2, LiCl-KCl-MgCl2 and NaCl-MgCl2 were used as molten chloride salts. The separation of Sr from the simulated oxide fuel was conducted by loading it in porous alumina basket and immersing it in a salt. The concentration of Sr in the salt was measured by ICP analysis after sampling the salt outside the basket using dip-stick technique. The separation efficiencies of Sr from simulated oxide fuel using the salts were compared. Furthermore, the causes of their separation efficiency were systematically investigated.

Facing the problem of saturation of spent nuclear fuel (SNF) stored in temporary storage facilities on sites, interest in the treatment of SNF is increasing, and it is recognized as a task that needs to be solved promptly. Although direct disposal is a general method for dealing with SNF, the entire fuel assembly is classified as high-level waste; thus, the burden of disposal is high. In order to minimize the disposal burden with enhancing safety for long term storage, it is necessary to develop SNF treatment technologies and continuous efforts are required from a national policy perspective. The present study focused on minimizing the volume of high level waste from light water reactor fuel by separation of uranium, which accounts for most of SNF. The chlorination characteristics of uranium (U), rare earth (RE) oxides were confirmed through lab-scale experiments, and the possibility of uranium separation from U-RE simulated fuel was evaluated using NH4Cl chlorinating agent. The detailed results will be posted and discussed.

In general, if a nuclear fuel cladding tube is damaged during reactor operation, it is called fuel failure. If the cladding tube is damaged, the function of sealing the nuclear fuel material is lost, and the fission products accumulated inside the nuclear fuel rod may leak into the coolant. The causes are the most damage caused by foreign substances in a coolant such as small iron wires, and GTRF (Gridto- Rod Wear) due to a grid, end-plug welding defect, PCMI (pellet cladding mechanical interaction), and oxidation corrosion damage. In this study, a device of simulating friction damage and debris induced damage between grid-fuel rods, which are the main causes of cladding tube damage, was developed. An air vibrator was installed as a function to induce vibration of the nuclear fuel rod. Sandpaper was installed between the grid and the fuel rod to induce friction between the grid-fuel rods. Saw teeth were installed on the grid to induce damage to foreign substances. It is believed that the simulated damaged nuclear fuel rod can be manufactured through on-study to provide the simulated damaged nuclear fuel rod necessary for the stabilization study of the damaged nuclear fuel rod.

KAERI의 PRIDE 시설에서 공학규모의 전해환원용 원료물질인 UO2 다공성펠렛 제조를 위해 공정과 장치를 최적화시킨 내 용을 다루었다. UO2 분말과 별도로 attrition 밀링된 대용산화물 분말을 출발분말로, 정밀 칭량을 통해 사용후핵연료 조성을 모사하였다(Simfuel). Simfuel 분말은 각각 tumbling mixer로 혼합하여 균질화 하고, rotary press로 성형하여 furnace를 이 용해 소결하였다. 4% H2-Ar 분위기에서 1450℃ 24시간 고온 열처리하여 제조된 소결펠렛은 6.89 g·cm-3의 벌크밀도를 가 지며 이는 후속 전해환원 공정의 요구에 부합한다. 소결된 다공성펠렛의 미세구조 관찰을 통해 다공성 기지상과 함께 산화/ 금속 석출물이 관찰되어 사용후핵연료의 상이 모사됨을 확인하였다. 본 결과는 향후 공학규모 이상의 파이로 연구를 위한 UO2 다공성펠렛 제조에 중요한 기초자료로 활용 될 것이다.

In order to investigate a nitriding process of spent oxide fuel and the subsequent change in thermal properties after nitriding, simulated spent fuel powder was converted into a nitride pellet with simulated fission product elements through a carbothermic reduction process. Nitriding rate of simulated spent fuel was decreased with increasing of the amount of fission products. Contents of Ba and Sr in simulated spent fuel were decreased after the carbothermic reduction process. The thermal conductivity of the nitride pellet was decreased by an addition of fission product element but was higher than that of the oxide fuel containing fission product elements.