With the recent concern regarding cellulose enhancing radionuclide mobility upon its degradation to ISA, disposal of cellulosic wastes is being held off until the disposal safety is vindicated. Thus, a rational assessment should be conducted, applying an appropriate cellulose degradation model considering the disposal environment and cellulose degradation mechanisms. In this paper cellulose degradation mechanisms and the disposal environment are studied to propose the best-suitable cellulose degradation model for the domestic 1st phase repository. For the cellulose to readily degrade, the pH should be greater than 12.5. As in the case of SKB, 1BLA is excluded from the safety assessment because the pH of 1BLA remains below 12.5. Furthermore, despite cellulose degradation occurring, it does not always produce ISA. At low Ca2+ concentration, the ISA yield rate is around 25%, but at high Ca2+ concentration, the ISA yield rate increases up to 90%. Thus, for the cellulose to be a major concern, both pH and Ca2+ concentration conditions must be satisfied. To satisfy both conditions, the cement hydration must be in 2nd phase, when the porewater pH remains around 12.5 and a significant amount of Ca2+ ion is leaching out from the cement. However, according to the safety evaluation and domestic research, 2nd phase of cement hydration for silo concrete would achieve a pH of around 12.4, dissatisfying cellulose degradation condition like in 1BLA. Thus, cellulose degradation would be unlikely to occur in the domestic 1st phase repository. To derive waste acceptance criteria, a quantitative evaluation should be conducted, conservatively assuming cellulose is degraded. To conduct a safety evaluation, an appropriate degradation model should be applied to determine the degradation rate of cellulose. According to overseas research, despite the mid-chain scission being yet to be seen in the experiments, the degradation model considering mid-chain scission is applied, resulting in an almost 100% degradation rate. The model is selected because the repositories are backfilled with cement, achieving a pH greater than 13, so extensive degradation is reasonably conservative. However, under the domestic disposal condition, where cellulose degradation is unlikely to occur, applying such model would be excessively conservative. Thus, the peeling and stopping model derived by Van Loon and Haas, which suggests 10~25% degradation rate, is reasonably conservative. Based on this model, cellulose would not be a major concern in the domestic 1st phase repository. In the future, this study could be used as fundamental data for planning waste acceptance criteria.

Concerns with colloids, dispersed 1~1,000 nm particles, in the LILW repository are being raised due to their potential to enhance radionuclide release. Due to their large surface areas, radionuclides may sorb onto mobile colloids, and drift along with the colloidal transport, instead of being sorbed onto immobile surfaces. To prevent adverse implications on the safety of the repository, the colloidal impact must be evaluated. In this paper, colloid analysis done by SKB is studied, and factors to be considered for the safety assessment of colloids are analyzed. First, the colloid generation mechanism should be analyzed. In a cementitious repository, due to a highly alkaline environment, colloid formation from wastes may be promoted by the decomposition of organic materials, dissolution of inorganic materials, and corrosion of metals. Radiolysis is excluded when radionuclide inventory is moderate, as in the case of SKB. Second, colloid stability should be evaluated to determine whether colloids remain in dispersion. Stable colloids acquire electric charges, allowing particles to continuously repel one another to prevent coagulation. Thus, stability depends on the pH and ionic condition of the surroundings, and colloid composition. For instance, under a highly alkaline cementitious environment, colloids tend to be negatively charged, repelling each other, but Ca2+ ion from cement, acting as a coagulant, makes colloid unstable, promoting sedimentation. As in the case of SKB, the colloidal impact is assumed negligible in the silo, BMA, and BTF due to their extensive cement contents, but for BLA, with relatively less cement source, the colloidal impact is a potential concern. Third, colloid mobility should be assessed to appraise radionuclide release via colloid transport. The mobility depends on the density and size of colloids, and flow velocity to commence motion. As a part of the assessment, the filtration effect should also be included, which depends on pore size and structure. As in the case of SKB, due to static hydraulic conditions and engineering barriers, acting as efficient filters, colloidal transport is expected to be unlikely. In the domestic underground repository, the highly alkaline environment would lead to colloid formation, but due to high Ca2+ concentration and low flow velocity, colloids would achieve low stability and mobility, thus colloidal impact would be a minor concern. In the future, with further detailed analysis of each factor, waste composition, and disposal condition, reliable data for safety evaluation could be generated to be used as fundamental data for planning waste acceptance criteria.

Many countries have used nuclear power to generate electricity. Uranium-235, which is used as fuel in nuclear power plants, produces many fission products. Among them, iodine-129 is problematic due to its long half-life (1.57×107 years) and high diffusivity in the environment. If it is released into the environment without any treatment, it could have a major impact on humans and ecosystems. Therefore, it must be treated into a stable form through capture and solidification. Iodine can be captured in the form of AgI through silver-loaded zeolite filters in off-gas treatment processes. However, AgI could be decomposed in the reducing atmosphere of groundwater, so it must be converted into a stable form. In this study, Al2O3, Bi2O3, PbO, V2O5, MoO3, or WO3 were added to the iodine solidification matrix, AgI-Ag2O-TeO2 glass. The glass precursors were mixed to the appropriate composition and placed in an alumina crucible. After heat treatment at 800°C for 1 hour, the melt was quenched in a carbon crucible. The leaching behavior and thermal properties of the glass samples were evaluated. The PCT-A test for leaching evaluation showed that the normalized releases of all elements were below 2 g/m2, which satisfied the U.S. glass wasteform leaching regulations. Diffrential scanning calorimetry (DSC) was performed to evaluate the thermal properties of all glass samples. The addition of MoO3 or WO3 to the AgI-Ag2O-TeO2 glass increased the glass transition temperature (Tg) and crystallization temperature (Tc) while maintaining the glass stability. The similar relative electro-static filed values of MoO3, and WO3 which are approxibately three times that of the glass network former TeO2, could provide sufficient force to the TeO2 interacting with the non-bridging oxygen forming Te-O-M (M=V, Mo, W) links. The high electrostatic forces of Mo and W increased the glass network cohension and prevented the crystallization of the glass.

Heat-generating nuclides such as Cs-137 and Sr-90 should be separated from spent nuclear fuel to reduce the short-term thermal load on the repository facility. In particular, Sr-90 must be separated because its decay process generates high temperatures. Recently, the Korea Atomic Energy Research Institute (KEARI) has been developing a waste burden minimization technology to reduce the environmental burden resulting from the disposal of spent nuclear fuel and maximize the utilization of the disposal facility. The technology incorporates a nuclide management process that maximizes disposal efficiency by selectively separating and accumulating key nuclides from spent nuclear fuel, such as Cs, Sr, I, TRU/RE, and Tc/Se. Sr nuclides dissolve in the chloride phase during the chlorination process of spent nuclear fuel and are recovered as carbonate or oxide through reactive distillation or reactive crystallization. Due to their chemical similarity, Ba nuclides are recovered along with Sr nuclides during this process. In this study, we prepared a ceramic waste form for group II nuclides, Ba(x)Sr(1-x)TiO3 (x=0, 0.25, 0.5, 0.75, 1), using the solid-state reaction method, taking into account the different ratios of Sr/Ba nuclides produced during the nuclide management process. Regardless of the Sr/Ba ratio, the established waste form fabrication process was able to produce a stable waste form. Physicochemical properties, including leaching and thermal properties, were evaluated to determine the stability of group II waste forms. In addition, the radiological properties of waste forms of Ba(x)Sr(1-x)TiO3 with varying Sr/Ba ratios were evaluated. These results provided fundamental data for the long-term storage and management of waste forms containing group II nuclides.

Hydrogen isotopes (H, D, T) separation technologies have received great interest for treatments of tritiated liquid waste produced in Fukushima. In addition, the separated deuterium and tritium can be utilized in various industries such as semiconductors and nuclear fusion as expensive and rare resources. However, separating hydrogen isotopes in gas and liquid forms still requires energyintensive processes. To improve efficiency and performance of hydrogen isotope separation, we are developing water electrolysis, cryosorption, distillation, isotope exchange, and hydrophobic catalyst technologies. Furthermore, an analytical method is studied to evaluate the separation of hydrogen isotopes. This presentation introduces the current status of hydrogen isotope research in this research group.

Boric acid-containing B-10 is used in a nuclear reactor as a coolant and absorbs thermal neutrons generated during nuclear fission in the primary circuit. Boron-containing coolant water waste is generated from maintenance, floor drain, decontamination, and reactor letdown flows. There are two options for aqueous solution waste of boric acid. One is recycling and discharge through filtration, ion exchange, and reverse osmosis. The other is immobilization after evaporation and crystallization processes. The dry powder of boric acid waste liquid can be immobilized by cement, polymer, etc. Before the mid-1990s, concentrated boric acid waste was solidified with a cement matrix. To overcome the disadvantage of low waste loading of cement waste form, a method of solidifying with paraffin was adopted. However, paraffin solids were insufficient to be disposed of as final waste. Paraffin is a kind of soft solidified material and has low compressive strength and poor leaching resistance. As a result, it was decided as an unsuitable form for disposal. In KOREA, paraffin waste form was adopted for boric acid waste treatment in the 1990s. A large amount of paraffin waste forms about 20,000 drums (200 l drum) were generated to treat boric acid waste and were stored in nuclear power sites without disposal. In this study, we want to obtain high-purity boric acid waste by oxidizing and decomposing solid paraffin waste form through a boric acid catalytic reaction. In this reaction, paraffin is separated in the form of various by-products, which can then be treated through a liquid waste treatment device or an exhaust gas treatment device. The proper temperature for sample decomposition during the catalytic reaction was set through TGA analysis. Compositions of by-products and residues generated at each stage of the reaction could be analyzed to determine the state during the reaction. Finally, the boric acid waste powder was perfectly separated from paraffin waste form with disposable products through this pyrolysis process.

This study introduces the licensing process carried out by the regulatory body for construction and operation of the 2nd phase low level radioactive waste disposal facility in Gyeongju. Also, this study presents the experience and lessons learned from this regulatory review for preparing the license review for the next 3rd phase landfill disposal facility. Korea Radioactive Waste Agency (KORAD) submitted a license application to Nuclear Safety and Security commission (NSSC) on December 24, 2015 to obtain permit for construction and operation of the national engineered shallow land disposal facility at Wolsong, Gyeongju. NSSC and Korea Institute of Nuclear Safety (KINS) started the regulatory review process with an initial docket review of the KORAD application including Safety Analysis Report, Radiological Environmental Report and Safety Administration Rules. After reflecting the results of the docket review, the safety review of revised 10 application documents began on November 29, 2016. Total 856 queries and requests for additional information were elicited by thorough technical review until November 16, 2021. As the Gyeongju and Pohang earthquakes occurred in September 2016 and November 2017, respectively, the seismic design of the disposal facility for vault and underground gallery was enhanced from 0.2 g to 0.3 g and the site safety evaluation including groundwater characteristics was re-investigated due to earthquake-induced fault. Also, post-closure safety assessments related to normal/abnormal/human intrusion scenarios were re-performed for reflecting the results of site and design characteristics. Finally, NSSC decided to grant a license of the 2nd phase low level radioactive waste disposal facility under the Nuclear Safety Laws in July 2022. This study introduces important issues and major improvements in terms of safety during the review process and presents the lessons learned from the experience of regulatory review process.

Glass wool, the primary material of insulation, is composed of glass fibers and is used to insulate the temperature of steam generators and pipes in nuclear power plants. Glass fiber is widely adopted as a substitute for asbestos classified as a carcinogen. The insulations used in nuclear power plants are classified as radioactive waste and most of the insulation is Very Low-Level Waste (VLLW). It is packaged in a 200 L drum the same as a Dry Active Waste (DAW). In the case of the insulations, it is packaged in a vinyl bag and then charged into the drum for securing additional safety because of the fine particle size of the fiberglass. A safety assessment of the disposal facility should be considered to dispose of radioactive waste. As a result of analyzing overseas Waste Acceptance Criteria (WAC), there is no case that has a separate limitation for glass fiber. Also, in order to confirm that glass fibers can be treated in the same manner as DAW, research related to the diffusion of glass fibers into the environment was conducted in this paper. It was confirmed that the glass fiber was precipitated due to the low flow velocity of groundwater in the Gyeongju radioactive waste repository and did not spread to the surrounding environment due to the effect of the engineering barrier. Therefore, the glass fiber has no special issue and can be treated in the same way as a DAW. In addition, it can be disposed of in the disposal facility by securing sufficient radiological safety as VLLW.

Se-79, a fission product of uranium, is present in spent nuclear fuel. Selenium is volatilized from the spent nuclear fuel during the pretreatment of pyroprocessing, and a filter composed of calcium oxide can capture gaseous selenium in the form of CaSeO3. Because Se-79 has a long half-life (3.27E5 years) and selenite ions have high mobility in groundwater, they must be immobilized in a chemically stable form for final disposal. This study used a composition of 50 TeO2 - 10 Al2O3 - 10 B2O3 - 10 Na2O - 10 CaO - 10 ZnO (mol%). High-purity powders of TeO2, Al2O3, H3BO3, Na2CO3, CaCO3, and ZnO were used as glass precursors. The mixed powders were placed in alumina crucibles and melted in an electric furnace under an ambient atmosphere at 800°C for 1 h before being cast on a carbon mold. The obtained glasses were ground into fine powders and then mixed with CaSeO3 powders. The powders were melted in alumina crucibles at 800°C for 1 h. To simulate a seleniumcaptured calcium filter, CaSeO3 was synthesized by a precipitation method using sodium selenite (Na2SeO3) and calcium nitrate (Ca(NO3)2) solutions. The glass samples were analyzed by an X-ray diffractometer (XRD). Retention of Se in tellurite glasses was analyzed by an X-ray fluorescence spectrometer (XRF) and inductively coupled plasma (ICP). The chemical durability of tellurite glass was evaluated through the PCT method.

Uranium-235, used in nuclear power generation, produces a lot of radioactive waste. Among radioactive waste nuclides, I-129 is problematic due to its long half-life (1.57×107 y) with high mobility in the environment. It should be captured and immobilized into a geological disposal environment through a stable waste form. In this study, various additives including Al, Bi, Pb, V, Mo and W were added to silver tellurite glass to prepare a matrix for immobilizing iodine, and its thermal and leaching properties were evaluated. To prepare glass, the glass precursor mixture was placed in alumina crucibles and heated at 800°C for 1 h. Except for aluminum, there was no significant loss of constituent elements. The loading of iodine in the matrix was approximately 11-15% by weigh, excluding oxygen. The normalized releases of all the elements obtained by PCT-A were below the order of 10-1 g/m2, which satisfies US regulation (2 g/m2). Differential scanning calorimetry was performed to evaluate the thermal properties of the glass samples. The glass transition temperature (Tg) increased by adding such as V2O5, MoO3, or WO3. The similar relative electrostatic field values of V2O5, MoO3, and WO3 could provide sufficient electro static field to the TeO2 interacting with the non-bridging oxygen forming Te-O-M (M = V, Mo, W) links. The addition of MoO3 or WO3 in the silver tellurite glass system increased glass transition temperature (Tg) and crystallization temperature (Tc) while maintaining the glass stability.