Highly radioactive waste is solidified to restrict leaching, retain its shape, and maintain its structural stability to prevent it from affecting humans and the environment as much as possible. This operation should be performed consistently regardless of whether the waste is homogeneous or heterogeneous. However, currently, there are no specific performance requirements for heterogeneous waste in Korea. This study reviewed domestic research results and the status of overseas applications, and proposed immobilization requirements for heterogeneous waste to be applied in Korea. IAEA safety standards, domestic laws, and waste acceptance criteria were reviewed. The status of heterogeneous waste immobilization in countries such as the United States, France, and Spain was reviewed. Most countries treat heterogeneous waste by encasing it in concrete, and impose immobilization requirements on this concrete. Based on these data, safety standards for the thickness, compressive strength, and diffusion limit of this concrete material were proposed as immobilization requirements for heterogeneous waste disposal in Korea. Quantitative values for the above requirements need to be derived through quantitative assessments based on the characteristics of domestic heterogeneous waste and disposal facilities.

Copper hexacyanoferrate (Cu-HCF), which is a type of Prussian Blue analogue (PBA), possesses a specific lattice structure that allows it to selectively and effectively adsorb cesium with a high capacity. However, its powdery form presents difficulties in terms of recovery when introduced into aqueous environments, and its dispersion in water has the potential to impede sunlight penetration, possibly affecting aquatic ecosystems. To address this, sponge-type aluminum oxide, referred to as alumina foam (AF), was employed as a supporting material. The synthesis was achieved through a dip-coating method, involving the coating of aluminum oxide foam with copper oxide, followed by a reaction with potassium hexacyanoferrate (KHCF), resulting in the in-situ formation of Cu-HCF. Notably, Copper oxide remained chemically stable, which led to the application of 1, 3, 5-benzenetricarboxylic acid (H3BTC) to facilitate its conversion into Cu-HCF. This was necessary to ensure the proper transformation of copper oxide into Cu-HCF on the AF in the presence of KHCF. The synthesis of Cu-HCF from copper oxide using H3BTC was verified through X-ray diffraction (XRD) analysis. The manufactured adsorbent material, referred to as AF@CuHCF, was characterized using Fourier-transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). These analyses revealed the presence of the characteristic C≡N bond at 2,100 cm-1, confirming the existence of Cu-HCF within the AF@CuHCF, accounting for approximately 3.24% of its composition. AF@CuHCF exhibited a maximum adsorption capacity of 34.74 mg/g and demonstrated selective cesium adsorption even in the presence of competing ions such as Na+, K+, Mg2+, and Ca2+. Consequently, AF@CuHCF effectively validated its capabilities to selectively and efficiently adsorb cesium from Cs-contaminating wastewater.

Various dry active wastes (DAWs) have been accumulated in nuclear power plants since the DAWs are mostly combustible. KAERI has developed a thermochemical treatment process for the used decontamination paper as an operational waste to substitute for incineration process and to decontaminate radionuclides from the DAWs. The thermochemical process is composed of thermal decomposition in a closed vessel, chlorination of carbonated DAWs, separation of soluble chlorides captured in water by hydroxide precipitation, and immobilization of the precipitate. This study examined the third and fourth steps in the process to immobilize Co-60 by fabricating a stable wasteform. Precipitation behaviors were investigated in the chloride solution by adding 10 M KOH. It was shown that the precipitates were composed of Mg(OH)2 and Al(OH)3. Then, the glass-ceramic wasteform for the precipitates were produced by adding additive mixtures in which silica and boron oxide were blended with various ratios. The wasteform was evaluated in terms of volume reduction ratio, bulk density, compressive strength, and leachability.

In general, radioactive waste with high radioactivity is made into a solid form with performance such as leaching restriction, shape retention, and structural stability so that radioactive waste does not affect humans and the environment as much as possible. This should be applied equally to radioactive waste, whether homogeneous or heterogeneous. The requirements are stipulated in the “Low and Intermediate Level Radioactive Waste Delivery Regulations” notice of the Korea Nuclear Safety and Security Commission. On the other hand, the waste acceptance criteria for domestic disposal facilities require immobilization of heterogeneous waste when the activity concentration is above a certain level, but do not provide specific immobilization performance requirements. In this study, the immobilization requirements applied to heterogeneous radioactive waste in various overseas countries operating low and intermediate-level radioactive waste disposal facilities were studied. First, the IAEA’s safety standards for radioactive waste immobilization, domestic regulations, and disposal facility waste acceptance criteria were reviewed. Countries operating surface disposal facilities such as the United States, France, Spain, and Japan and countries operating underground disposal facilities such as Sweden and Finland were divided to review the current status of immobilization application to heterogeneous waste in overseas countries. When reviewing overseas cases, each country’s disposal methods, types of disposal waste, and waste treatment criteria were also reviewed. It was found that the immobilization requirements for heterogeneous radioactive waste vary depending on the disposal method and the type of barrier used to ensure disposal safety in each country. The common point is to surround heterogeneous radioactive waste within a concrete lining of a certain thickness, and to apply the thickness, compressive strength, and diffusion coefficient of the concrete lining as immobilization performance requirements. Through this study, the immobilization performance requirements for heterogeneous radioactive waste in various overseas countries that stably operate low- and intermediate-level radioactive waste were confirmed, which is expected to contribute to specifying the performance requirements for immobilization of heterogeneous radioactive waste in domestic disposal facilities.

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.

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.

Radioactive cesium is a heat generated and semi-volitile nuclide in spent nuclear fuel (SNF). It is released gasous phase by head-end treatment which is a pretreatment of pyroprocessing. One of the capturing methods of gasous radioactive cesium is using zeolite. After ion-exchanged zeolite, it is transformed to ceramic waste form which is durable ceramic structure by heat treatment. Various ceramic wasteforms for Cs immobilization have been researched such as cesium aluminosilicate (CsAlSi2O6), cesium zirconium phosphate (CsZr2(PO4)3), cesium titanate (CsxAlxTi8-xO16, Cs2TiNb6O18) and CsZr0.5W1.5O6. The cesium pollucite is composed to aluminosilicate framework and cesium ion incorporated in matrix materials lattices. Many researchers are reported that the pollucite have high chemical durability. In this study, the Cesium pollucite was fabricated using mixtures of aluminosilicate denoted Absorbent product (AP) and Cs2CO3 by calcination and pelletized by cold pressing. The characterization of fabricated pollucite powder and pellets was analyzed by XRD, TGA, SEM, SEMEDS and XRF. The chemical durability of pollucite powder was evaulated by PCT-A and ICP-MS and OES. Thus, the optimal pressure condition without breaking the pellets which is low Cs2O/AP ratio and pelletizing pressure was selected. The long-term leaching test was performed using MCC-1 method for 28 days with the fabricated pollucite pellets. The leachate of leaching test was allard groundwaster and Deionized water and replaced 5 contact periods which is 3 hours, 3 days, 7 days, 14 days and 28 days and analyzed by ICPMS. The leaching rate was shown two stages. The first stage was rapid and relatively large amount of nuclides were leached. The leaching rate was decreased in the second stage. The fractional release rate of this study was shown same trend. These results were similar to previous studies.

The number of nuclear power plants that are permanently shut down or decommissioned is increasing worldwide, and accordingly, research is being conducted on an appropriate method for disposing of radioactive waste generated during the decommissioning of nuclear power plants. In the case of waste liquid generated during the decommissioning of nuclear power plants, it is important not only to efficiently reduce waste but also to secure the suitability of disposal. One of the solidification treatment methods for radioactive waste is cement solidification, but since cement solidification has poor solidification properties and generates a large amount of waste, improvement activities have been pursued. This study aims to develop high-performance cement-based materials and solidification treatment technology for solidification of liquid radioactive waste generated during nuclear decommissioning in order to improve the problems of cement solidification treatment method. For the development of polymer cement, epoxy resin and polyamine/amide mixed type and general Portland cement were mixed in various ratios. The most appropriate mixing ratio was 4.5:2, which showed the highest compressive strength. A simulated waste liquid was prepared by referring to the preliminary decommissioning plan of Shin-Kori Units 5 and 6, and it was dried and made into granules. Polymer cement was injected into a drum filled with granules by vacuum pressure to prepare a waste form matrix. In the solidification process, granules made by drying the waste liquid were used, and the solidification agent was filled in between the granules, so the total volume of solid radwaste was reduced compared to the conventional cement solidification treatment method. As a result, the amount of waste decreased to about 1/3, and the volume reduction rate increased by about 2.2 times. The compressive strength of 3,243 psi was confirmed in the disposability performance test for the manufactured solid samples. The compressive strength after the thermal cycling test, irradiation test, microorganism test, and immersion test was 2,257 psi, 2,306 psi, 4,530 psi, and 2,263 psi, respectively, exceeding the acceptance criteria of 500 psi. The leaching index was 7~13, and no free standing water was generated.

Radioactive carbon, C-14, can be generated by the neutron capture reaction of O-17 during the nuclear power plant operation. Since C-14 is classified as an intermediate level waste radionuclide, it is required that an effective separation process for C-14. C-14 is mainly absorbed on activated carbon in the air cleanup system. Therefore, the main generation source of C-14 during the nuclear power plant decommissioning is spent activated carbon. KAERI has been developing the treatment of spent activated carbon. In this process, C-14 can be desorbed as a gaseous oxide form from the spent activated carbon at high-temperature vacuum conditions. This radioactive carbon dioxide can be captured into alkaline earth metal incorporated glass and can be transformed into carbonate form. However, the carbonate (e.g. CaCO3 and SrCO3) is dispersive. When the radioactive carbonates are disposed into a geological repository, they should be immobilized to remove future uncertainty. This study examined the stabilization/immobilization of the radioactive carbonates by the cement hydration process. Cement wasteform incorporated with calcium carbonate and strontium carbonate was produced under various waste loading (e.g. 20wt%, 40wt%, and 60wt% of CaCO3 and SrCO3, respectively). Then we evaluated mechanical and chemical durability by measuring compressive strength and leachability according to standard test methods specified in the waste acceptance criteria of the Gyeongju low and intermediate level waste repository (WAC-SIL-2022-1). Also, microstructure and thermal characteristics were investigated by SEM-EDS and TGA analysis.

Uranium-235, used for nuclear power generation, has brought radioactive waste. It could be released into the environment during reprocessing or recycling of the spent nuclear fuel. Among the radioactive waste nuclides, I-129 occurs problems due to its long half-life (1.57×107 y) with high mobility in the environment. Therefore, it should be captured and immobilized into a geological disposal system through a stable waste form. One of the methods to capture iodine in the off-gas treatment process is to use silver loaded zeolite filter. It converts radioactive iodine into AgI, one of the most stable iodine forms in the solid state. However, it is difficult to directly dispose of AgI itself in an underground repository because of its aqueous dissolution under reducing condition with Fe2+. It must be immobilized in the matrix materials to prevent release of iodine as a result of chemical reaction. Among the matrix glasses, silver tellurite glass has been proposed. In this study, additives including Al, Bi, Pb, V, Mo, and W were added into the silver tellurite glass. The thermal properties of each matrix for radioactive iodine immobilization were evaluated. The glasses were prepared by the melt-quenching method at 800°C for 1 h. Differential scanning calorimetry (DSC) was performed to evaluate the thermal properties of the glass samples. From the study, the glass transition temperature (Tg) was increased by adding additives such as V2O5, MoO3, or WO3 in the silver tellurite glass. The relative electro-static field (REF) values of V2O5, MoO3, and WO3 are about three times higher than that of the glass network former, TeO2. It could provide sufficient electro-static field (EF) to the TeO2 interacting with the non-bridging oxygen forming Te-O-M (M = V, Mo, W) links. Therefore, the addition of V2O5, MoO3, or WO3 reinforced the glass network cohesion to increase the Tg of the glass. The addition of MoO3or WO3 in the silver tellurite glass increased Tg and crystallization temperature (Tc) with remaining the glass stability.

Immobilization of radioactive borate waste containing a high boron concentration using cement waste form has been challenged because the soluble borate phase such as boric acid reacts with calcium compounds, hindering the hydration reaction in cement waste form. Metakaolin-based geopolymer waste form which has a pure aluminosilicate system without calcium can be a promising alternative for the cement; however, secondary B-O-Si networks are formed by a reaction between borate and silicate, resulting in poor mechanical characteristics such as low compressive strength and final setting retardation. Thus, it is important to optimize the Si/Al molar ratio and curing temperature which are critical parameters of geopolymer waste form to increase borate waste loading and enhance the durability of geopolymer. Here, metakaolin-based geopolymer waste form to immobilize simulant radioactive borate waste was fabricated by varying the Si/Al molar ratio and curing temperature. The 7 days-compressive strength results reveals that the Si/Al molar ratio of 1.4 and curing at 60°C is advantageous to achieving high waste loading (30wt%). In addition, geopolymer waste forms with the highest borate waste loading exceeded the 3.445 MPa after the waste form acceptance criteria such as thermal cycling, gamma irradiation, and water immersion tests. The leachability index of boron was 7.56 and the controlling leaching mechanism was diffusion. The thermal cycling and gamma irradiation did not significantly change the geopolymer structure. The physically incorporated borate waste was leached out from geopolymer waste form during leaching and water immersion tests. Considering these results, metakaolin-based geopolymer waste form with a low Si/Al ratio is a promising candidate for borate waste immobilization, which has been difficult using cement.

Activated carbon (AC) injection has been regarded as one of the most effective control technologies for Hg0 removal in flue gas. It is worthwhile to explore new and simple preparation methods for AC with low cost and high Hg removal capacity. In this study, a biomass based AC was successfully prepared from levant cotton exocarp using ZnCl2 activation. The mercury adsorption efficiency and mechanism were studied via the fixed bed experiments. Activator, reaction temperature and components of simulated coal-fired flue gas were investigated. Brunauer–Emmett–Teller (BET), scanning electron microscopy with energy-dispersive X-ray spectrometry (SEM–EDX) and X-ray photoelectron spectroscopy (XPS) were applied for morphology characterization of the prepared AC and discussion of the possible adsorption mechanism. The adsorbed mercury species and the physiochemical properties of prepared AC were discussed. The results showed that (1) Hg0 removal efficiency could reach up to 90% at 150 ℃ under simulated flue gas (SFG); (2) Hg0 adsorption was controlled by the combination of physical and chemical mechanisms.