The growing significance of sustainable energy technologies underscores the need for safe and efficient management of spent nuclear fuels (SNFs), particularly via deep geological disposal (DGD). DGD involves the long-term isolation of SNFs from the biosphere to ensure public safety and environmental protection, necessitating materials with high corrosion resistance for DGD canisters. This study investigated the feasibility of a Cu–Ni film, fabricated via additive manufacturing (AM), as a corrosion-resistant layer for DGD canister applications. A wire-fed AM technique was used to deposit a millimeter-scale Cu–Ni film onto a carbon steel (CS) substrate. Electrochemical analyses were conducted using aerated groundwater from the KAERI underground research tunnel (KURT) as an electrolyte with an NaCl additive to characterize the oxic corrosion behavior of the Cu–Ni film. The results demonstrated that the AM-fabricated Cu–Ni film exhibited enhanced corrosion resistance (manifested as lower corrosion current density and formation of a dense passive layer) in an NaCl-supplemented groundwater solution. Extensive investigations are necessary to elucidate microstructural performance, mechanical properties, and corrosion resistance in the presence of various corroding agents to simplify the implementation of this technology for DGD canisters.

Buffer materials play an important role in preventing the leakage of radionuclides from the residue. The mineralogical properties of these buffer materials are critical in repository design. This study presents the fundamental properties of Na-type MX80 and a novel Ca-type Bentonil- WRK. The CaO to MgO ratio in Bentonil-WRK was approximately 1:1, and the CaO to Na2O ratio was approximately 2.8:1. These results suggest that Bentonil-WRK demonstrates a lower swelling index compared to Gyeongju bentonite due to its CaO-to-MgO ratio’s proximity to 1:1, despite having a higher montmorillonite content than Gyeongju bentonite. The results of this research can provide useful foundational data for the evaluation of the thermal-hydraulic-mechanical-chemical behavior of buffer materials.

Corrosion cells that simulates engineering barrier system have been stored in an aerobic KURT environment for 10 years, which were recovered and dismantled in 2021. The test specimens were compressed copper (Com. Cu), Cold spray copper (CSC Cu), Ti Gr.2, STS 304, and Cast nodular iron. The specimens were buffered by compact Ca-type Gyeongju bentonite (KJ-I) and compact Na-type Wyoming bentonite. And the corrosion cells were exposed to KURT groundwater at 30°C for about 10 years (3,675 days). As a result of the long-term experiment in aerobic environment, it was confirmed that Na-bentonite is more advantageous for inhibiting corrosion than Ca-bentonite. The corrosion thickness of the most specimens in Ca bentonite was slightly lower than in Na bentonite until the initial 500 days, but after 10 years, the corrosion thickness of copper and cast iron specimens in Na bentonite was clearly lower. The corrosion thickness of the copper specimen in Na bentonite was very low about 0.5 um in both Com. Cu and CSC Cu. Moreover, the corrosion thickness in Ca bentonite was very high about 4 um for Com. Cu and 6 um for CSC Cu. In the case of cast iron, the corrosion thickness in Na bentonite was about 13 um, and 15 um in Ca bentonite. The common feature of copper and cast iron specimens in Ca bentonite, which showed a high corrosion thickness, is the forming of a white mineral deposition layer on the specimen surface, which was presumed to be some kind of feldspar. On the other hand, it was found that the STS304 and Ti specimens were hardly corroded even after 10 years. In conclusion, when a white mineral deposition layer was formed on the specimen surface, the corrosion thickness always increased sharply than before, and thus it was estimated that the generation of the mineral deposition layer cause the increase of bentonite permeability, and rather the weakening of existing passive corrosion film.

Li-Cd 합금을 이용한 환원추출방식을 LiCl-KCl 기반의 drawdown 공정에 적용하게 되면, LiCl-KCl 공융염의 조성이 파괴되므로 공정온도를 높여야 하며, 전해정련 및 전해제련과 같은 공정에 LiCl-KCl 용융염을 재사용할 수 없게 된다. 따라서, 본 연구에서는 공융염 조성에 적합한 Li-K-Cd 합금을 제조하였으며, 이를 이용하여 U와 Nd가 포함된 LiCl-KCl 염에 투입하여 용 융염 내 UCl3의 제거가 가능한지 평가하였다.