One of released radioactive gases from a spent fuel is cesium (137Cs) as semi-volatile fission products and reticulated ceramic foam could be used for capturing the gaseous cesium. It has threedimensional open-pore structures and consumes cesium above 600°C to form cesium species including Cs-nepheline (CsAlSiO4) and pollucite (CsAlSi2O6) phases. Kaolinite-based foam filter is a favorable ceramic filter because they exhibit superior capture characteristics compared to other aluminosilicate minerals and other shape filters. However, for usage in special conditions, structural limitations such broken struts must be improved. Here, recoating by using centrifugation, followed by a pre-sintering cycle was conducted for covering the cracks and voids, resulting from the burnout of the polyurethane sponge as a sacricial template. The slurry including additives was chosen by considering viscous behavior of slurries for the centrifugation. The microstructure and strength was improved by the recoating.

Reticulated foams have a continuous skeleton network consisting of aluminosilicates and are used for capturing gaseous cesium released from spent nuclear fuel at high temperature. It has high stability to high temperature and good capturing performance. Homogeneous cell distribution and modified surface structures are indispensable conditions for stable operation and handling. In particular, triangularly shaped holes inside the struts were generated during the pyrolysis of polyurethane sponge as a sacricial template, which lead to limite the strength of the reticulated foam as well as cracks. However, several attempts have been focused on the increasing the strut thickness. Here, we have prepared ceramic foams by the polyurethane sponge replication method with roller squeezing. Ceramic slurry including additives was determined with consideration of its viscous behavior. After pre-sintering, infiltration under vacuum was conducted. Metakaolin slurry was filled partially into the triangular void. As a result, the compression strength was improved by structure modification without composition change.

Globally, the operation of nuclear power plants results in the production of a tremendous quantity of spent nuclear fuel. The methods for handling spent nuclear fuel can be categorized into three: storage, direct disposal and recycling. A technology designed to recycle accumulated spent nuclear fuel is pyropocessing. In pyroprocessing, various fission products (FPs) such as C-14, H-3, I-129 and Cs-137 are generated. Among these FPs, technetium (Tc-99) is a gaseous nuclear isotope with a long half-life and high mobility in the form of TcO4 - in aqueous solutions, making it essential to capture strictly in order to prevent radioactive contamination of the environment. In previous studies, ion-exchange or adsorption using MOFs (Metal Organic Frameworks) have been used to remove Tc-99. These methods, however, involve separation in aqueous solutions, not in the gaseous state. In this study, we developed a CaO-based adsorbent for capturing Re as a surrogate for radioactive Tc-99. Isopropyl alcohol (IPA) was employed as a pore-forming agent during the preparation of the adsorbents, and its effects on characteristics and adsorption performance were investigated. The size of the pores were analyzed from nitrogen (N2) adsorption isotherm analysis and mercury (Hg) intrusion curves. As a result, it was confirmed that the addition of IPA had a significant impact on the formation of macro-pores. Furthermore, this macroporous structure was found to enhance the adsorption performance of Re.

The disposal of spent nuclear fuel (SNF) poses a significant challenge due to its high radioactivity and heat generation. However, SNF contains reusable materials, such as uranium and trans-uranium, which can be recovered through aqueous reprocessing or pyrochemical processes. Prior to these processes, voloxidation is necessary to increase reaction kinetics by separating fuels from cladding and reducing the particle size. In the voloxidation, uranium dioxide (UO2) from SNF is heated in the presence of oxygen and oxidized to triuranium octoxide (U3O8), resulting a release of gaseous fission products (FPs), including technetium-99 (Tc-99), which poses a risk to human health and the environment due to its high mobility and long half-life of 2.1×105. To date, various methods have been developed to capture Tc in aqueous solutions. However, a means to capture the gaseous form of Tc (Tc2O7) is essential in the voloxidation. Due to the radioactive properties of technetium isotopes, rhenium is often used as a substitute in laboratory settings. The chemical properties of rhenium and technetium, such as their electronic configurations, oxidation states, and atomic radii, are similar and these similarities indicates that the adsorption mechanism for rhenium can be analogous to that for technetium. In the previous study, a disk-type adsorbent based on CaO developed was effective in capturing Re. However, this study lacked sufficient data on the chemical properties and capture performance of the adsorbent. Furthermore, the fabrication of disk-type adsorbents is time-consuming and requires multiple steps, making it impractical for mass production. This study introduces a simple and practical method for preparing CaO-based pellets, which can be used as an adsorbent to capture Re. The results provide a better understanding of the adsorption behavior of CaO-based pellets and their potential for capturing Tc-99. To the best of our knowledge, this is the first study to apply a CaO-based pellet to capture Re and investigate its potential for capturing Tc-99.

The stabilization techniques are highly required for damaged nuclear fuel to strengthen safety in terms of transportation, storage, and disposal. This technique includes recovering fuel materials from spent fuel, fabrication of stabilized pellets, and fabrication of fuel rods. Thus, it is important to identify the leaching behavior of the stabilized pellets to verify their stability in humid environments which are similar to storage conditions. In this study, we introduce various leaching experiment methods to evaluate the leaching behavior of the stabilized pellets, and determine the most suitable leaching test methods for the pellets. Also, we establish the leaching test conditions with various factors that can affect the dissolution and leaching behavior of the stabilized pellets. Accordingly, we prepare the simulated high- (55 GWd/tU) and low- (35 GWd/tU) burnup nuclear fuel (SIMFUEL) and pure UO2 pellets sintered at 1,550°C and 1,700°C, respectively. Each pellet is placed in a vessel and filled with DI water and perform the leaching test at three different temperature to verify the leaching mechanism at different temperature range. Based on the standard leaching test method (ASTM C1308-21), the test solution is removed from the pellet after specific time intervals and replaced in the fresh water, and the vessel is placed back into the controlled-temperature ovens. The test solutions are analyzed by using ICP-MS.

Molten Salt Reactor (MSR) is one of Generation-IV nuclear reactors that uses molten salts as a fuel and coolant in liquid forms at high temperatures. The advantages of MSR, such as safety, economic feasibility, and scalability, are attributed from the fact that the molten salt fuel in a liquid state is chemically stable and has excellent thermo-physical properties. MSR combines the fuel and coolant by dissolving the actinides (U, Th, TRU, etc.) in the molten salt coolant, eliminating the possibility of a core meltdown accident due to loss of coolant (LOCA). Even if the molten salt fuel leaks, the radioactive fission products dissolved in the molten salt will solidify with the fuel salt at room temperature, preventing potential leakage to the outside. MSR was first demonstrated at ORNL starting with the Aircraft Reactor Experiment (ARE) in 1954 and was extended to the 7.4 MWth MSRE developed in 1964 and operated for 5 years. Recently, various start-ups, including TerraPower, Terrestrial Energy, Moltex Energy, and Seaborg, have been conducting research and development on various types of MSR, particularly focusing on its inherent safety and simplicity. While in the past, fluoride-based molten salt fuels were used for thermal neutron reactors, recently, a chlorine-based molten salt fuel with a relatively high solubility for actinides and advantageous for the transmutation of spent nuclear fuel and online reprocessing has been developing for fast neutron spectrum MSRs. This paper describes the development status of the process and equipment for producing highpurity UCl3, a fuel material for the chlorine-based molten salt fuel, and the development status of the gas fission product capturing technologies to remove the gaseous fission products generated during MSR operation. In addition, the results of the corrosion property evaluation of structural materials using a natural circulation molten salt loop will also be included.

Molten Salt Reactor, which employs molten salt mixture as fuel, has many advantages in reactor size and operation compared to conventional nuclear reactor. In developing Molten Salt Reactor, Offgas system should be properly designed since the fission products in off-gas accelerates the corrosion in reactor structure materials and deteriorates the purity of liquid fuel. The design of off-gas system therefore requires the preliminary study of the behavior of evolved fission products in off-gas units and the development of off-gas model is crucial in developing such system. In this study, we corrected the off-gas illustrative model proposed by ORNL (Nuclear Engineering and Design, vol 385(15) 111529, 2021) by employing physically consistent concept of capture rate of fission product and holdup. For the application of the corrected off-gas model to Chloride-based 6 MW Molten Salt Reactor, major fission products were firstly determined from OpenMC based neutronics calculation and chain reaction related to the major fission products were defined. Based on these data, the holdup behavior of fission products in off-gas units (decay tank, caustic scrubber, Halide trap, H2O trap and charcoal bad) were investigated.

An accumulation of spent nuclear fuel (SNF) has brought a considerable interest due to its energy and environmental issue. To effectively manage SNF, a pyroprocessing is introduced to separate useful resources from the spent fuels and to manufacture suitable fuels. In head-end process of pyroprocessing, spent fuels are thermally treated to prepare UO2 pellets, where various radioactive gases from SNFs are released during thermal treatment. Within these gases, C-14 as CO2 form is a radioactive fission product which had a long half-life of 5,730 years and emits beta radiation of 0.156 MeV. Generally, current CO2 capturing technologies include adsorption by solid materials, absorption by aqueous solutions, and membrane separation. Among these methods, absorption is an effective approach which traps CO2 effectively and and it is easy to operate at room temperature. In addition, it is highly recommended as immobilizing 14CO2 as CaCO3 formation due to the high thermal and chemical stability, and the relatively low solubility in water. Generally, a double alkali method has been proposed to capture low concentrated 14CO2 from the stream. This method for CO2 capture includes absorption process with NaOH solution and causticization using Ca(OH)2. In this study, CO2 emitted from SNF is captured using double alkali method, and the effects of operating conditions on capturing efficiency were investigated. Furthermore, considering the two-film theory, the effects of trapping conditions on the CO2 absorption performance were examined. The recovered CaCO3 from causticization was collected from the absorbing solution and analyzed.