We conducted safety assessments for the disposal of spent resin mixed waste after the removal of beta radionuclides (3H, 14C) in a landfill facility. The spent resin tank of Wolsong nuclear power plant is generated by 8:1:1 weight ratio of spent ion exchange resin, spent activated carbon and zeolite. Waste in the spent resin tank was classified as intermediate-level radioactive waste due to 14C. Other nuclides such as 60Co and 137Cs exhibit below the low-level radioactive waste criteria. The techniques for separating mixed waste and capturing 14C have been under development, with a particular focus on microwave-based methods to remove beta radionuclides (3H, 14C) from spent activated carbon and spent resin within the mixed waste. The spent resin and activated carbon within the waste mixture exhibits microwave reactivity, heated when exposed to microwaves. This technology serves as a means to remove beta isotopes within the spent resin, particularly by eliminating 14C, allowing it to meet the low-level radioactive waste criteria. Using this method, the waste mixture can meet disposal requirements through free water and 3H removal. These assessments considered the human intrusion scenarios and were carried out using the RESRAD-ONSITE code. The institutional management period after facility closure is set at 300 years, during which accidental exposures resulting from human intrusion into the disposal site are accounted for. The assessment of radiation exposure to intruders in a landfill facility included six human intrusion scenarios, such as the drilling scenario, road construction scenario, post-drilling scenario, and post-construction scenario. Among the six human intrusion scenarios considered, the most conservative assessment about annual radiation exposure was the post-drilling scenario. In this scenario, human intrusion occurs, followed by drilling and residence on the site after the institutional management period. We assumed that some of the vegetables and fruits grown in the area may originate from contaminated regions. Importantly, we confirmed that radiation doses resulting from post-institutional management period human intrusion scenarios remain below 0.1 mSv/y, thus complying with the annual dose limits for the public. This research underscores the importance of effectively managing and securing radioactive waste, with a specific focus on the safety of beta radionuclide-removed waste during long-term disposal, even in the face of potential human intrusion scenarios beyond the institutional management period.

The sustainability of the nuclear power industry hinges increasingly on the safe, long-term disposal of radioactive waste. Despite significant innovations and advancements in nuclear fuel and reactor design, the quest for a permanent solution to handle accumulating radioactive waste has received comparatively less attention. Conventionally, two widely recognized solidification methods, namely cementation for low and intermediate-level waste and vitrification for high-level waste, have been favored due to their simplicity, affordability, and availability. Recently, geopolymers have emerged as an appealing alternative, gaining attention for their minimal carbon footprint, robust chemical and mechanical properties, cost-effectiveness, and capacity to immobilize a broad spectrum of radionuclides, including radioactive organic compounds. This study delves into the synthesis of metakaolin-based geopolymers tailored for the immobilization of fission products like cesium (Cs) and molybdenum (Mo). The investigation unfolded in two key steps. In the initial step, we optimized the alkali content to prevent the occurrence of efflorescence, a potential issue. Remarkably, as the Na2O/Al2O3 ratio increased from 0.82 to 1.54, we observed significant enhancements in both compressive strength (11.45 to 27.07 MPa) and density (up to 2.23 g/cm3). This suggests the importance of careful adjustment in achieving the desired geopolymer characteristics. The second phase involved the incorporation of 2wt% of Cs and Mo, both individually and as a mixture, into the geopolymer matrix. We prepared the GP paste, which was poured into cylindrical molds and cured at 60°C for one week. To scrutinize the crystallinity, phase purity, and bonding type of the developed matrix, we employed XRD and FTIR techniques. Additionally, we conducted standard compressive strength tests (following ASTM C39/C39M-17b) to assess the stacking durability and robustness of the developed waste form, vital for storage, handling, transportation, and disposal in a deep geological repository. Furthermore, to evaluate the chemical durability, diffusivity and leaching of the GP waste matrix, we employed the ASTM standard Product Consistency Test (PCT: C 1285-02) and American nuclear society’s devised leaching test (ANS 16.1). It is noteworthy that the introduction of Cs and Cs/Mo in the GP matrix led to a reduction of more than 50% and 60% in compressive strength, respectively. This outcome may be attributed to the interference of Cs and Mo with the geopolymerization process, potentially causing the formation of new phases. However, it is crucial to emphasize that both developed matrices exhibited an acceptable normalized leaching rate of less than 10-5 g·m-2·d-1. This finding underscores the promising potential of the GP matrix for the immobilization of cationic and anionic radioactive species, paving the way for more sustainable nuclear waste management practices.

Nuclear power plants use ion exchange resins to purify liquid radioactive waste generated while operating nuclear power plants. In the case of PHWR, ion exchange resins are used in heavy water and dehydration systems, liquid waste treatment systems, and heavy water washing systems, and the used ion exchange resins are stored in waste resin storage tanks. The C-14 radioactivity concentration in the waste resin currently stored at the Wolseong Nuclear Power Plant is 4.6×106 Bq/g, exceeding the low-level limit, and if all is disposed of, it is 1.48×1015 Bq, exceeding the total limit of 3.04×1014 Bq of C-14 in the first stage disposal facility. Therefore, disposal is not possible at domestic low/medium-level disposal facilities. In addition, since the heavy water reactor waste resin mixture is stored at a ratio of about 20% activated carbon and zeolite mixture and about 80% waste resin, mixture extraction and separation technology and C-14 desorption and adsorption technology are required. Accordingly, research and development has been conducted domestically on methods to treat heavy water waste resin, but the waste resin mixture separation method is complex and inefficient, and there are limitations in applying it to the field due to the scale of the equipment being large compared to the field work space. Therefore, we would like to introduce a resin treatment technology that complements the problems of previous research. Previously, the waste resin mixture was extracted from the upper manhole and inspection hole of the storage tank, but in order to improve limitations such as worker safety, cost, and increased work time, the SRHS, which was planned at the time of nuclear power plant design, is utilized. In addition, by capturing high-purity 14CO2 in a liquid state in a high-pressure container, it ensures safety for long-term storage and is easy to handle when necessary, maximizing management efficiency. In addition, the modularization of the waste resin separation and withdrawal process from the storage tank, C-14 desorption and monitoring process, high-concentration 14CO2 capture and storage process, and 14CO2 adsorption process enables separation of each process, making it applicable to narrow work spaces. When this technology is used to treat waste resin mixtures in PHWR, it is expected to demonstrate its value as customized, high-efficiency equipment that can secure field applicability and safety and reflect the diverse needs of consumers according to changes in the working environment.

Radioactive iodine-129, a byproduct of nuclear fission in nuclear power plants, presents significant environmental and health risks due to its high solubility in water and volatility. Iodine-129, with its half-life of 1.57×1017 years, necessitates safe management and disposal. Therefore, safely capturing and managing I-129 during spent nuclear fuel reprocessing is of paramount importance. To address these challenges, various glass waste forms containing silver iodide have been developed, such as borosilicate, silver phosphate, silver vanadate, and silver tellurite glasses. These glasses effectively immobilize iodine, but the high cost of silver raises affordability concerns. This study introduces CuI·Cu2O·TeO2 glass waste forms for iodine immobilization, a novel approach. The cost-effectiveness of copper, in contrast to silver, makes it an attractive alternative. The CuI·Cu2O·TeO2 glass waste forms were synthesized with varying CuI content (x) in (1-x)(0.3Cu2O·0.7TeO2) glass matrices. Xray diffraction (XRD) confirmed amorphous structures, and X-ray fluorescence (XRF) quantified composition. X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy provided insights into structural properties. Durability assessments using a 7-day product consistency test (PCT-A) and inductively coupled plasma-mass spectrometry (ICP-MS) revealed compliance with U.S. glass regulations, making CuI·Cu2O·TeO2 glasses a promising choice for iodine immobilization in radioactive waste.

Ion exchange resins are commonly employed in the treatment of liquid radioactive waste generated in nuclear power plants (NPP). The ion exchange resin used in NPP is a mixed-bed ion exchange resin known as IRN-150, which is of nuclear grade. This resin is a mixture of cation exchange resin and anion exchange resin. The cation exchange resin removes cationic radionuclides such as Cs and Co, while anion exchange resin handles anions (e.g., H14CO3 -), effectively purifying the liquid waste. Spent ion exchange resins (spent resin) containing C-14 are classified as low and intermediate level radioactive waste, and their radioactivity needs to be reduced as it exceeds the disposal limit regulated by law. Therefore, the microwave technology for the removal of C-14 from spent resin has been investigated. Previous studies have successfully developed a method for the effective removal of C-14 during the resin treatment process. However, it was observed that, in this process, functional groups in the resin were also removed, resulting in the generation of off-gases containing trimethylamine. These off-gases can dissolve in water from process, increasing its pH, which can subsequently hinder the recovery of C-14. In this study, we investigated the high-purity recovery of C-14 by adjusting the moisture content within the reactor following microwave treatment. Mock spent resins, consisting of 100 g of resin with HCO3 - ion-exchanged and 0, 25, or 50 g of deionized water, were subjected to microwave treatment for 40 or 60 minutes. Subsequently, the C-14 desorption efficiency of the mock spent resins was evaluated using an acid stripping process with H3PO4 solution. The functional group status of the mock spent resins was analyzed using 15N NMR spectroscopy. The results showed that the mock spent resins exhibited efficient C-14 recovery without significant functional group degradation. The highest C-14 desorption efficiency was achieved when 25 g of deionized water was used during microwave treatment.

The primary objective of this study is to evaluate a systematic design’s effectivity in remediating actual uranium-contaminated soil. The emphasis was placed on practical and engineering aspects, particularly in assessing the capabilities of a zero liquid discharge system in treating wastewater derived from soil washing. The research method involved a purification procedure for both the uranium-contaminated soil and its accompanying wastewater. Notably, the experimental outcomes demonstrated successful uranium separation from the contaminated soil. The treated soil could be self-disposed of, as its uranium concentration fell below 1.0 Bq·g−1, a level endorsed by the International Atomic Energy Agency for radionuclide clearance. The zero liquid discharge system’s significance lay in its distillation process, which not only facilitated the reuse of water from the separated filtrate but also allowed for the self-disposal of high-purity Na2SO4 within the residues of the distilled filtrate. Through a comparative economic analysis involving direct disposal and the application of a remediation process for uranium-contaminated soil, the comprehensive zero liquid discharge system emerged as a practical and viable choice. The successful demonstration of the design and practicality of the proposed zero liquid discharge system for treating wastewater originating from real uranium-contaminated soil is poised to have a lasting impact.

In order to evaluate the exposure dose of residents living near nuclear power plants, a Off-site Dose Calculation Program (ODCP) has been developed based on SAP since 2021. The ODCP consists of social environmental factor, atmospheric diffusion factors, liquid/gas dose evaluation, and comprehensive analysis, and was developed by dividing it into functional modules. The offsite dose calculation can be carried out monthly, quarterly, semi-annual, and annual, and resident dose evaluation is conducted by entering air diffusion factors and emissions for each period. It also enables comprehensive evaluation result management by developing history management functions together.

Domestic nuclear power plants can affect the environment if multiple devices are operated on one site and even a trace amount of pollutants that may affect the environment after power generation are simultaneously discharged. Therefore, not only radioactive substances but also ionic substances such as boron should be discharged as minimally as possible. We adopted pilot CDI and SD-ELIX sytem to separating and concenrating of boron containing nulcear power plant discharge water. The boron concentration of the initial inflow water tended to decrease over time. The water quality of concentrated water also reached its peak until the initial 60 minutes, but tended to decrease in line with the decrease in the inflow water concentration. The boron removal rate was in the range of 85 to 99% with respect to the initial boron concentration of 15 to 25 mg/L. On the other hand, performance degradation due to the use of electrochemical modules is also observed, and regeneration through low ion-containing water cleaning effective. We shortened processing time by considering the optimal flow rate conditions and conductivity conditions and converting electrochemical modules into series or parallel.

The development of existing radioactive waste (RI waste) management technologies has been limited to processing techniques for volume reduction. However, this approach has limitations as it does not address issues that compromise the safety of RI waste management, such as the leakage of radioactive liquid, radiation exposure, fire hazards, and off-gas generation. RI waste comes in various forms of radioactive contamination levels, and the sources of waste generation are not fixed, making it challenging to apply conventional decommissioning and disposal techniques from nuclear power plants. This necessitates the development of new disposal facilities suitable for domestic use. Various methods have been considered for the solidification of RI waste, including cement solidification, paraffin solidification, and polymer solidification. Among these, the polymer solidification method is currently regarded as the most suitable material for RI waste immobilization, aiming to overcome the limitations of cement and paraffin solidification methods. Therefore, in this study, a conceptual design for a solidification system using polymer solidification was developed. Taking into account industrial applicability and process costs, a solidification system using epoxy resin was designed. The developed solidification system consists of a pre-treatment system (fine crush), solidification system, cladding system, and packing system. Each process is automated to enhance safety by minimizing user exposure to radioactive waste. The cladding system was designed to minimize defects in the solidified material. Based on the proposed conceptual design in this paper, we plan to proceed with the specific design phase and manufacture performance testing equipment based on the basic design.

There is a large amount of radioactive waste in waste storage in the Korea Atomic Energy Research Institute. Some of the radioactive waste was generated during the dismantling process due to Korea Research Reactor 1&2 and it accounts for 20% of the total waste. Radioactive waste must be reduced by appropriate disposal methods to secure storage space and to reduce disposal costs. Research Reactor wastes include wastes that are below the acceptable criteria for selfdisposal and non-contaminated wastes, so they can be treated as wastes subject to self-disposal through contamination analysis and reclassification. In order to deregulation radioactive waste, it is necessary to meet the self-disposal standards stipulated in the Domestic Nuclear Act and the treatment standards of the Waste Management Act. The main factors of deregulation are surface contaminant, radionuclide activity and dose assessment. To confirm the contamination of waste, surface contaminant and gamma nuclide analysis were performed. After homogenizing the waste sample, it was placed in 1 L Mariinelli beaker. When collecting waste samples, 1 kg per 200 kg of waste was collected. The concentrations of the major radionuclides Co-60, Cs-134, Cs-137, Eu-152, and Eu-154 were analyzed using HPGe detector. To evaluate radiation dose, various computational programs were used. A dose assessment was performed with the analyzed nuclide concentration. The concentrations of representative nuclides satisfied the deregulation acceptance criteria and the results of the dose assessment corresponding to self-disposal method was also satisfied. Based on this results, KAERI submitted the report on waste self-disposal plan to obtain approval. After final approval, Research Reactor waste is to be incinerated and incineration ash is to be buried in the designated place. Some metallic waste has been recycled. In this study, the suitability of deregulation for self-disposal was confirmed through the evaluation of the surface contaminant analysis, radionuclide concentration analysis and dose assessment.

Radioactive waste is typically disposed of using standard 200 and 320 L drums based on acceptance criteria. However, there have been no cases evaluating the disposal and suitability of 200 L steel drums for RI waste disposal. There has been a lack of prior assessments regarding the disposal and suitability of 200 L steel drums for the disposal of RI waste. Radioactive waste is transported to disposal facilities after disposal in containers, where the drums are loaded and temporarily stored. Subsequently, after repackaging the disposal drums, the repackaged drums are transported to disposal facilities by vehicle or ship for permanent disposal. Disposal containers can be susceptible to damage due to impacts during transportation, handling, and loading, leading to potential damage to the radiation primer coating during loading. Additionally, disposal containers may be subject to damage from electrochemical corrosion, necessitating the enhancement of corrosion resistance. Metal composite coatings can be employed to enhance both abrasion resistance and corrosion resistance. The application of metal composite coatings to disposal containers can improve the durability and radiation shielding performance of radioactive waste disposal containers. The thickness of radioactive waste disposal containers is determined through radioactive shielding analysis during the design process. The designed disposal containers undergo structural analysis, considering loading conditions based on the disposal environment. This paper focuses on evaluating the structural improvements achieved through the implementation of metal composite coatings with the goal of enhancing corrosion and abrasion resistance.

The decommissioning of nuclear power plants will generate a lot of low and intermediate-level radioactive waste (LILW), and preliminary radioactive evaluation for these wastes should be carried out before decommissioning work. Mainly, Concrete, Carbon Steel, Stainless Steel-304 (SS304) and Inconel are used in many parts of nuclear power plants and considered as main resource of nuclear wastes. Depending on the material location, the number of neutrons irradiated to material varies, which can range from self-disposal waste to LILW. In this paper, activation analysis was performed to compare the radiation dose according to the presence or absence of impurity elements present in SS304. For the calculation, SS304 composition and impurity elements were used as described in the report of NUREG-3474. This report lists 41 impurity elements for SS304 and other materials. Calculation code is used ORIGEN-S module in SCALE 6.1 code. Neutron flux is used as arbitrary value that around 1E+11 level and irradiation time is set as 30 year with 10-year cooling time. In the ORIGEN-S calculation, 1g of SS304 is used for easy calculation of specific activity. The ORIGEN-S calculation results are as follows. All impurity elements contained case calculated 9.32E+07 Bq activity. In the absence of all impurity elements case and most cases shows that total Becquerel value after 10-year cooling time around 9.11E+07 Bq, and Co impurity case had larger result. The calculation was performed again by increasing the amount of impurity substances by 100 times to perform the sensitivity evaluation more reliably. Representatively, Li, N, Co, and Ba impurity elements cases were calculated to have a particularly high Becquerel. Especially Co impurity element case, a total Becquerel of 3.03E+08 was calculated. Accordingly, evaluation of impurities mixed in SS304 must be considered, and in particular, the inclusion rate for Co must be considered.

Among the nuclear power plant facility improvement projects, out of a total 10 replacement reactor vessel closure head (RRVCH), five have been replaced, starting with Gori Unit 1, and five, including Hanul Unit 1, Hanbit Units 5 and 6, and Hanul Units 3 and 4 will be replaced in the future. This paper presents the method of treating Latch Housing among radioactive waste generated during the replacement of Hanul Unit 2 (February 2023). Latch Housing controls the control rod by receiving magnetic force from the CRDM’s Coil Stack. Located in the Old Reactor Vessel Head (ORVH) Hot Spot, the range of measured radiation dose rate was 0.3 to 0.8 mSv h-1 (up to 4.5 mSv h-1). The amount of radioactive waste generated was 35.8 Baler-Drum (based on 200L), and the order of treatment was to cut into the Omega Seal of the CRDM, the CRDM and Latch Housing Transfer, the boundary of the CRDM and Latch Housing, the Rod Travel Housing, the Motor Housing and the Latch Assembly, and then transfer and Drumming. In the United States, out of 93 operating reactors, 31 reactor vessel heads have been replaced and 19 reactor vessel heads are scheduled to be replaced. In Korea, 25 reactors are in operation, and two reactors have been permanently shut down. Among them, the nine old reactors for more than 30 years (as of September 2021) are expected to achieve ALARA and reduce radwaste management costs through the management method applied to replace the reactor vessel head.

Low- and intermediate level waste (LILW) repository in Gyeongju, Korea is in operation and the radioactive waste should satisfy the waste acceptance criteria (WAC) of the repository. Among the WAC of the Gyeongju LILW repository, the leachability index criterion is considered to be the criterion that is directly related to the isolation of the radionuclides from biosphere. Cesium, strontium, and cobalt should satisfy the leachability index larger than six by following the ANS 16.1 leaching test method. Several research were performed for the leachability index of Cs, Sr, and Co by following the ANS 16.1 leaching test method. However, the test condition of the previous research is expected to be different to the condition of the actual waste. Due to the radioactivity of the radionuclide such as Cs, Sr and Co, most of the research applied the surrogate of those radionuclides. The concentration of those nuclides was generally measured by the inductively coupled plasma (ICP) equipment, however, high concentration compared to the disposal limit of those nuclides due to the detection limit of the ICP was applied. From the Freundlich and Langmuir adsorption isotherms, the adsorption of the nuclides differs according to the concentration of the nuclides. As the leachability index of the nuclides is affected by the adsorption of the nuclides on the binding material, the effect of nuclide concentration is expected to be not ignorable. Therefore, the leachability index difference according to the nuclide concentration should be compared to avoid over- or underestimation of the leachability index. In this study, the difference in the leachability index according to the concentration of nuclides is aimed to be checked. Cs, Sr, and Co, which should satisfy the leachability index criterion in the WAC of the Gyeongju repository, were selected as target nuclides. Three concentrations were selected to compare the leachability index: 0.1 mol, 0.001 mol and below the regulatory exemption concentration. The concentration of non-radioactive nuclides in the leachant was measured by ICPOES and ICP-MS while the concentration of radionuclides was measured by HPGe. The result of this study can be applied as background data enhancing the WAC or disposal concentration limit of the radionuclides in Gyeongju LILW repository.

This study focuses on the development of coatings designed for storage containers used in the management of radioactive waste. The primary objective is to enhance the shielding performance of these containers against either gamma or neutron radiation. Shielding against these types of radiation is essential to ensure the safety of personnel and the environment. In this study, tungsten and boron cabide coating specimens were manufactured using the HVOF (High-Velocity Oxy Fuel) technuqe. These coatings act as an additional layer of protection for the storage containers, effectively absorbing and attenuating gamma and neutron radiation. The fabricated tungsten and boron carbide coating specimens were evaluated using two different testing methods. The first experiment evaluates the effectiveness of a radiation shielding coating on cold-rolled steel surfaces, achieved by applying a mixture of WC (Tungsten Carbide) powders. WC-based coating specimens, featuring different ratios, were prepared and preliminarily assessed for their radiation shielding capabilities. In the gamma-ray shielding test, Cs-137 was utilized as the radiation source. The coating thickness remained constant at 250 μm. Based on the test results, the attenuation ratio and shielding rate for each coated specimen were calculated. It was observed that the gammaray shielding rate exhibited relatively higher shielding performance as the WC content increased. This observation aligns with our findings from the gamma-ray shielding test and underscores the potential benefits of increasing the tungsten content in the coating. In the second experiment, a neutron shielding material was created by applying a 100 μm-thick layer of B4C (Boron Carbide) onto 316SS. The thermal neutron (AmBe) shielding test results demonstrated an approximate shielding rate of 27%. The thermal neutron shielding rate was confirmed to exceed 99.9% in the 1.5 cm thick SiC+B4C bulk plate. This indicates a significant reduction in required volume. This study establishes that these coatings enhance the gamma-ray and neutron shielding effectiveness of storage containers designed for managing radioactive waste. In the future, we plan to conduct a comparative evaluation of the radiation shielding properties to optimize the coating conditions and ensure optimal shielding effectiveness.

Activated carbon (AC), extensively used across various industrial sectors, serves as a sponge for different types of gases due to its porous carbon material. These gases are attracted to the carbon substrate via van der Waals forces. In nuclear power plants, AC is commonly used to adsorb radioactive gases such as 86Kr and 134Xe, as well as radioiodine sources like 131I and 133I from gaseous effluents. Even if the adsorbed radioactive gases and radioiodine decay into non-radioactive elements, the spent AC still contains radioactive species with long half-lives, such as 3H (Tritium, T) and 14C (radiocarbon). Minimizing and separating waste that contains long-lived nuclides (e.g., 14C) are pivotal components of an efficient waste management approach. A challenging aspect of effectively managing disposed AC is to minimize long-lived radioactive substances by eliminating them. This paper explores and summarizes the technology used to remove pollutants (3H, 14C) trapped within the pores of Activated carbon through thermochemical vacuum and surface oxidation processes. By recycling and reusing spent Activated carbon, we anticipate a reduction in the volume of radioactive waste, leading to decreased disposal costs. Furthermore, this paper will contribute as a valuable reference in future studies, enhancing the understanding of vacuum thermal desorption and surface oxidation of used Activated carbon.

At the end of 2022 there were 439 nuclear power reactors in operating around the world, including 25 nuclear power reactors of Korea. Domestic nuclear power plants (NPPs) continuously produce low and intermediate-level radioactive waste (LILW) and spent nuclear fuel (SNF). As amount of radioactive waste is increasing and interim storage facilities meet limitation of their capacity, radioactive waste need to be transported. Consequently, the demand for radioactive waste transportation is increasing and the importance of Radiation Risk Assessment Codes (RRACs) for radioactive waste transportation is also on the rise. Considering the domestic situation where all NPPs are located on seaside, the radioactive waste transportation by ship is inevitable and the its risk assessment is very important for safety. Although various researches on radioactive waste transportation risk assessment is being actively conducted, research on domestic radioactive waste maritime transportation is insufficient. In this study, MARINRAD and KM-RAD were used to review on the radioactive waste transportation risk assessment. The result of reviewing shows that MARINRAD used SNF as transporting radioactive materials and ‘SAND87-7067 (1987)’ as nuclide database, whereas KMRAD used LILW and ‘IAEA Technical Report Series-422 (2004)’. To complement these limitations, we present an modernized integrated database by updating data and covering the radioactive materials from LILW to SNF. These results are expected to contribute to the development of RRACs for domestic radioactive waste maritime transportation.

Activated carbon (AC) is used for filtering organic and radioactive particles, in liquid and ventilation systems, respectively. Spent ACs (SACs) are stored till decaying to clearance level before disposal, but some SACs are found to contain C-14, a radioactive isotopes 5,730 years halflife, at a concentration greater than clearance level concentration, 1 Bq/g. However, without waste acceptance criteria (WAC) regarding SACs, SACs are not delivered for disposal at current situation. Therefore, this paper aims to perform a preliminary disposal safety examination to provide fundamental data to establish WAC regarding SACs SACs are inorganic ash composed mostly of carbon (~88%) with few other elements (S, H, O, etc.). Some of these SACs produced from NPPs are found to contain C-14 at concentration up to very-low level waste (VLLW) criteria, and few up to low-level waste (LLW) criteria. As SACs are in form of bead or pellets, dispersion may become a concern, thus requiring conditioning to be indispersible, and considering VLL soils can be disposed by packaging into soft-bags, VLL SACs can also be disposed in the same way, provided SACs are dried to meet free water requirement. But, further analysis is required to evaluate radioactive inventory before disposal. Disposability of SACs is examined based on domestic WAC’s requirement on physical and chemical characteristics. Firstly, particulate regulation would be satisfied, as commonly used ACs in filters are in size greater than 0.3 mm, which is greater than regulated particle size of 0.2 mm and below. Secondly, chelating content regulation would be satisfied, as SACs do not contain chelating chemicals. Also, cellulose, which is known to produce chelating agent (ISA), would be degraded and removed as ACs are produced by pyrolysis at 1,000°C, while thermal degradation of cellulose occurs around 350~600°C. Thirdly, ignitability regulation would be satisfied because as per 40 CFR 261.21, ignitable material is defined with ignition point below 60°C, but SACs has ignition point above 350°C. Lastly, gas generation regulation would be satisfied, as SACs being inorganic, they would be targeted for biological degradation, which is one of the main mechanism of gas generation. Therefore, SACs would be suitable to be disposed at domestic repositories, provided they are securely packaged. Further analysis would be required before disposal to determine detailed radioactive inventories and chemical contents, which also would be used to produce fundamental data to establish WAC.

Kori Unit 1 was permanently shut down in 2017 and is currently being prepared for decommissioning. Decommissioning waste generated during the decommissioning of a nuclear power plant has the characteristic of being generated in large quantities over a short period. Therefore, if proper management is not carried out, abnormal situations (i.e., unauthorized disposal, diversion, etc.) may occur. According to IAEA General Safety Report Part 6, radioactive waste shall be managed for all waste streams in decommissioning. This means ensuring that all waste streams are managed by the recorded inventory of all decommissioning waste and verifying that the recorded inventory is reasonable. The radioactive waste management has been managed in units such as mass and radioactivity. However, in the case of decommissioning waste, the amount is very large, so management by radioactivity is expected to have limitations. Therefore, in this study, a simple test was conducted to verify the decommissioning waste generated by a hypothetical scenario by mass. In this study, establish a scenario assuming various flows of decommissioning waste expected to be generated and calculate the expected inventory of decommissioning waste using Microsoft Excel. Specifically, using “Material Unaccounted For” (MUF), a material balance equation in IAEA Services Series 15, Nuclear Material Accounting Handbook, the error inventory was calculated as the difference between the physical inventory of decommissioning waste in the area and the ending inventory. We propose a simple test scenario to verify the flow of decommissioning waste by verifying that the error inventory reasonably matches the set allowable error. This study aims to verify the inventory of decommissioning waste using the material balance methodology used for nuclear material accounting. It is expected that the safety and reliability of the nuclear power plant decommissioning process can be secured by verifying that the total inventory of equipment before decommissioning and the inventory of remaining equipment and decommissioning waste after decommissioning are reasonably consistent.

In nuclear power plant environments, the analysis of gamma-emitting waste materials with complex shapes can be challenging. ISOCS (In-Situ Objective Counting System) is employed to measure the gamma-emitting radionuclide concentrations. However, it is crucial to validate the accuracy of ISOCS measurements. This study aims to validate the accuracy of ISOCS measurement results for spent filters. The ISOCS measurement process begins with modeling and efficiency calculations of the target spent filters using ISOCS software. ISOCS offers the advantage of direct measurement assessment by incorporating shielding materials and collimators into the detector efficiency calculation during the modeling process, without the need for separate efficiency correction sources. To validate the accuracy of ISOCS measurement results, the measured radioactivity values were used as input data for the MicroShield computer code to derive dose rates. These dose rates were then compared to the dose rates measured on-site, confirming the reliability of ISOCS measurements. In the field, ISOCS gamma measurements and surface dose rates were measured for three Cavity filters and four RCP Seal Injection filters. The measured dose rate for the Cavity filters was around 270 Svhr, and the computed values using MicroShield showed an error of approximately 12%. Despite modeling and calculation errors in computer analysis and potential uncertainties in the measurement environment and instrument, the computed values closely matched the measured values. However, the measured dose rate for the RCP Seal Injection filters ranged 2.9~8 Svhr, which is very low and close to background levels. When compared to the results of computer analysis, an error ranging from 27% to 97% was observed. It is concluded that validating the accuracy in the low dose rate range close to background levels is challenging through a comparison of calculated and measured dose rates.