Noble metal phase, present in used fuel, are fission products that can be found as metallic precipitates in used nuclear fuel. They exist as small particles (nm~um) in grain boundaries of the used fuels. Since they are particles deposited between the grain structures, they can be considered as defects in the pellet structure. Thermal expansion of fuels with noble metal is slightly higher than that of bare fuels. The fuels at high temperature, such as immediately after being discharged from nuclear reactors, may be subject to fuel failure if sufficient cooling is not provided. Recent research has shown that the noble metals can migrate into the rim space between the pellet and the cladding, and be deposited in the inner layer of the claddings. therefore, the mechanical integrity of the cladding can be degraded by noble metals, as well as the pellets. The concentration of the noble metal phase should be considered to evaluate the effect of the noble metals on the fuel integrity, after discharge from the reactors. SCALE/ORIGEN code was used to evaluate the noble metals in fuel assembly-scale, and the radial distribution in the fuel assembly. The radial distribution of the reactor power was derived from the SCALE/TRITON, considering Westinghouse 17×17. Square cell model was chosen for the geometry and 1/4 model was applied to reduce the computation time.

Noble metal precipitates are fission products that can be found as metallic alloys in used nuclear fuel. They do not exist homogenously inside the fuel pellets, but exists in grain boundaries in the form of immiscible particles. The first drawback that comes because they exist in grain boundaries is the degradation of mechanical integrity. The particles in the grain boundaries can be considered as defect n solid solution of uranium oxide pellets, and they can change the lattice volume. Therefore, it is known that it can cause stress corrosion cracking of fuel pellets. Furthermore, there is a negative effect from the perspective of used fuel management. However, they also have a positive effect on used fuel management. Since the noble metal has galvanic reduction effect, the particles serve as an oxidation inhibitor for uranium. There are many other effects regarding to the noble metal precipitates. However, in any case, quantifying the particles is important in order to quantitatively analyze these effects from the perspective of used fuel management. SCALE/TRITON code was applied to calculate the noble metal isotopes including Mo, Tc, Ru, Rh and Pd. In order to calculate the distribution inside the pin, the multiregion cell model was selected. In particular, a cylindrical geometry was used, and the pellet was divided into several layers. In addition, coolant and cladding surrounded the pellet. Finally, the radial distribution was evaluated using the computational code, along with neutron flux map.

Al-B4C neutron absorbers are currently widely used to maintain the subcriticality of both wet and dry storage facilities of spent nuclear fuel (SNF), thus long-term and high-temperature material integrity of the absorbers has to be guaranteed for the expected operation periods of those facilities. Surface corrosion solely has been the main issue for the absorber performance and safety; however, the possibility of irradiation-assisted degradation has been recently suggested from an investigation on Al-B4C surveillance coupons used in a Korean spent nuclear fuel pool (SFP). Larger radiation damage than expectation was speculated to be induced from 10B(n, α)7Li reactions, which emit about a MeV α-particles and Li ions. In this study, we experimentally emulated the radiation damage accumulated in an Al-B4C neutron absorber utilizing heavy-ion accelerator. The absorber specimens were irradiated with He ions at various estimated system temperatures for a model SNF storage facility (room temperature, 150, 270, and 400°C). Through the in-situ heated ion irradiation, three exponentially increasing level of radiation damages (0.01, 0.1, and 1 dpa or displacement per atom) were achieved to compare differential gas bubble formation at near surface of the absorber, which could cause premature absorber corrosion and subsequential 10B loss in an SNF storage system. An extremely high radiation damage (10 dpa), which is unlikely achievable during a dry storage period, was also emulated through high temperature irradiation (350°C) to further test the radiation resistance of the absorber, conservatively. The irradiated specimens were characterized using HR-TEM and the average size and number density of radiation-induced He bubbles were measured from the obtained bright field (BF) TEM micrographs. Measured helium bubble sizes tend to increase with increasing system (or irradiation) temperature while decrease in their number density. Helium bubbles were found from even the lowest radiation damage specimens (0.01 dpa). Bubble coalescence was significant at grain boundaries and the irradiated specimen morphology was particularly similar with the bubble morphology observed at the interface between aluminum alloy matrix and B4C particle of the surveillance coupons. These characterized irradiated specimens will be used for the corrosion test with high-temperature humid gas to further study the irradiation-assisted degradation mechanism of the absorber in dry SNF storage system.

Irradiated uranium dioxide in damaged used fuel could oxidize during transportation, interim storage or disposal, resulting that the fuel pellet fragments are reduced to a grain-sized powder that can easily escaped from the damaged rod. It has been reported that oxidized spent fuel (i.e. U4O9+x) that was in contact with water could increase the dissolution rate by making the grain boundaries more accessible to the water. Therefore, the damaged used fuel requires stabilization technology including nuclear material recovery, pellet manufacturing process, and stabilization fuel rod manufacturing that can secure safety in terms of permanent disposal. In this study, we prepared pure UO2 and SIMFUEL pellets that are a mixture of UO2 and surrogated metallic oxides for fission products equivalent to a burn-up of 35 GWd/tU and 55 GWd/tU as the stabilized spent fuel. The UO2 and fission products powders were milled and pressed into pellets at 250 MPa and sintered at 1,550°C and 1,700°C for 6 hours in an atmosphere of 4%H2-Ar. The prepared UO2 and SIMFUEL pellets were placed in PTFE Teflon vessels and filled with deionized water to identify the leaching behavior by a long-term leaching experiment under the similar condition to a repository for the safe disposal.

An options study was performed for the treatment of residual elemental sodium in driver plenums following the chopping operation during the pyroprocessing of used nuclear fuel. Given the pending availability of a multi-function furnace for distillation and consolidation operations in the Fuel Conditioning Facility, the furnace was considered for the processing of driver plenums. Although two options (oxidation and distillation) could be performed in the multi-function furnace, neither option has been developed sufficiently to date to warrant the use of the furnace for treatment operations. Thus, it was decided to defer the treatment of elemental sodium from driver plenums in the multi-function furnace until more developed technologies and/or furnaces become available. In the interim, storage of the plenums and characterization efforts are recommended.

Plasma carbon blacks of 20~30 nm diameter were synthesized by direct decomposition of natural gas using a hybrid plasma torch system with 50 kW direct current and 4 MHz of radio frequency. The insulating rector which inside diameter of 400 mm and length of 1500 mm, respectively was kept at 300~400℃ during the preparation. The ultimate analysis of plasma carbon blacks reveals that the raw plasma carbon blacks contains a large quantity of volatile which is mainly consist of hydrogen. Therefore devolatilization of raw plasma carbon blacks were carried out at 900℃ for one hour under nitrogen atmosphere. The devolatilization leads to the decrease in electrical resistivity and surface oxygen functional groups of plasma carbon black significantly. In order to investigate the plasma carbon as a catalyst support, devolatilized plasma black at 900℃ (DPB) supported PtAu catalyst was synthesized by sodium boronhydride reduction method. Electrochemical measurements and direct formic acid fuel cell test indicated that catalytic activity of DPB supported PtAu catalyst for formic acid oxidation was similar to that of Vulcan XC-72 of commercial carbon black supported one.

국산 핵연료에 사용되는 KOFA Zircaloy-4피복관의 조사성장 거동을 평가하고 제조 공정이 서로 다른 Siemens사 피복관의 조사성장거동과 비교하기 위하여 고리 2호기에 장전된 핵연료 피복관의 조사성장이 측정되었다. KOFA Zircaloy-4피복관은 최종 열처리시의 부분 재결정화로 인하여 fully annealed Zircaloy피복관고 Siemens사 피복관의 측정된 조사성장율이 차이는 제조공정의 차이에 기인한 피복관 집합도 계수의 차이로서 설명할 수 있었다. 고리 2호기 국산핵연료에서 측정된 자료를 이용하여 KOFA Zircaloy-4 피복관의 2단계 조사성장 모델이 유도되었는데 향후 측정자료가 많이 축적되면 유도된 모델의 정확성이 보다 명확하게 검증될 수 있을 것이다.