The process of carbonization followed by a high-temperature halogenation removal of radionuclides is a promising approach to convert low-radioactivity spent ion-exchange (IE) resins into freereleasable non-radioactive waste. The first step of this process is to convert spent ion-exchange resins into the carbon granules that are stable under high-temperature and corrosive-gas flowing conditions. This study investigated the kinetics of carbonization of cation exchange resin (CER) and the changes in structures during the course of carbonization to 1,273 K. Both of model-free and modelfitted kinetic analysis of mixed reactions occurring during the course of carbonization were first conducted based on the non-isothermal TGAs and TGA-FTIR analysis of CER to 1,272 K. The structural changes during the course of carbonization were investigated using the high-resolution FTIR and C-13 NMR of CER samples pyrolyzed to the peak temperature of each reaction steps established by the kinetic analysis. Four individual reaction steps were identified during the course of carbonization to 1,273 K. The first and the third steps were identified as the dehydration and the dissociation of the functional group of —SO3-H+ into SO2 and H2O, respectively. The second and the fourth steps were identified as the cleavage of styrene divinyl benzene copolymer and carbonization of pyrolysis product after the cleavage, respectively. The temperature and time positions of the peaks in the DTG plot are nearly identical to those of the peaks of the Gram Schmidt intensity of FTIR. The structural changes in carbonization identified by high-resolution FTIR and DTG are in agreement with those by C-13 NMR. The results of a detailed examination of the structural changes according to NMR and FTIR were in agreement with the pyrolysis gas evolution characteristics as examined by TGA-FTIR.

In all geodisposal scenarios it is key to understand the interaction of radionuclides with mineral particles during their formation/recrystallisation. Studying processes at the molecular scale provides insight into long-term radionuclide behaviour. Uranium is a significant radionuclide in higher activity wastes destined for geological disposal, and iron (oxyhydr) oxides (e.g. goethite, 􀟙-FeOOH). are ubiquitous in and around these systems, formed via processes including metal corrosion and microbially induced reactions. There are numerous reports of uranium-incorporation into iron (oxyhydr) oxides, therefore it has been suggested that they may be a barrier to uranium migration in geodisposal systems. However, long-term stability of these phases during environmental perturbations are unexplored. Specifically, U-incorporated iron (oxyhydr) oxide phases may interact with Fe(II) and sulphide from biological or geological origin. Firstly, electron transfer occurs between adsorbed Fe(II) and iron oxyhydroxides, with potential for changes in the speciation of incorporated uranium e.g. oxidation state changes and/or release. Secondly, on exposure to aqueous sulfide, iron (oxyhydr) oxides undergo reductive dissolution and recrystallisation to iron sulphides. Understanding the fate of incorporated uranium during these process in key to understanding its long term behaviour in subsurface systems. A series of experimental studies were undertaken where U(VI)-goethite was synthesized then reacted with either aqueous Fe(II) or S(-II), and the system monitored over time using geochemical analysis and X-ray absorption spectroscopy (XAS) techniques e.g. U LIII-edge and MIV-edge HERFD-XANES. Reaction with aqueous Fe(II) resulted in electron transfer between Fe(II) and U(VI)-goethite, with > 50% U(VI) reduced to U(V). XAS analysis revealed that U remained within the goethite structure, and electron transfer only occurred within the outermost atomic layers of goethite. which led to U reduction. Rapid reductive dissolution of U(VI)-goethite occurred on reaction with sulfide at pH7. A transient release of aqueous U was observed during the first day, likely due to uranyl(VI)-persulfide species. However, U was retained in the solid phase in the longer term. In contrast, the sulfidation of U adsorbed to ferrihydrite at pH 12.2 led to the immediate release of U (< 10% Utotal) associated with a colloidal erdite (NaFeS2·2H2O) phase. Moreover, in the bulk phase the surface of ferrihydrite was passivated by sulfide, and U was found to have been trapped within surface associated erdite-like fibres. Overall, these studies further understanding of the long-term behaviour of U-incorporated iron (oxyhydr)oxides supporting the overarching concept of iron (oxyhydr) oxides acting as a barrier to U migration.

In the decommissioning site of Korean Research Reactor 1&2 (KRR-1&2), according to Low and Intermediate-level Radioactive Waste Disposal Acceptance Criteria of the Korea Radioactive Waste Agency (WAC-SIL-2022-1), characteristics of radioactive waste was conducted on approximately 550 drums of concrete and soil waste for a year starting from 2021. Among them, 50 drums of concrete waste transported and disposed to Gyeongju LILW disposal facility at the end of 2022. For the remaining approximately 500 drums of concrete and soil waste stored on-site, they were reclassified into two categories: permanent disposal grade and clearance grade. This classification was based on calculating the sum of fractions (SOF) per drum for each radionuclides. The plan is to dispose of around 200 drums in the permanent disposal grade and about 300 drums in the clearance grade by the end of 2023. Since concrete and soil decommissioning wastes are generated in large quantities over a short period with similar origins, they were grouped within five drums as suggested by the acceptance criteria. Mixed samples were collected from each group and used for radionuclide analysis. When utilizing mixed samples, three distinct samples are collected and analyzed for each group. The maximum value among these three radionuclide analysis results is then uniformly applied as the radionuclide concentration value for all drums within that group. Radioactive nuclides contained in similar types of radioactive waste with similar origins can be expected to have some statistical distribution. However, There has been no verification as to whether the maximum value among the three mixed samples exists within the statistical distribution or if it deviates from this distribution to represent a different value. In this study, we confirmed characteristics of radionuclide concentration distribution by examining and comparing radionuclide concentration distributions for radioactive wastes drum grouped for nuclear characteristic among 50 concrete wastes drum disposed in year 2022 and 500 concretes & soils drum scheduled for disposal (clearance or permanent disposal) in year 2023. In particular, when comparing tritium to other nuclides, it was observed that the standard deviation for the distribution of maximum values was approximately 318 times larger.

KAERI has developed a Radioactive Waste Information Management System (RAWINGS) to manage the life-cycle information from the generation to the disposal of radioactive waste, in compliance with the low- and medium-level radioactive waste acceptance criteria (WAC). In the radioactive waste management process, the preceding steps are to receive waste history from the waste generators. This includes an application for a specified container with a QR label, pre-inspection, and management request. Next, the succeeding steps consist of repackaging, treatment, characterization, and evaluating the suitability of disposal, for a process to transparently manage radioactive wastes. Since the system operated in 2021, The system is enhanced to manage dynamic information, including the tracking of the location of radioactive waste and the repackaging process. Small packages of waste could be classified as either radioactive or clearance waste during pre-inspection. Furthermore, waste generated in the past has already been packaged in drums, and a new algorithm has been developed to apply the repackaging when reclassification is required. All radioactive waste with the unique ID number on the specific container is managed within a database, the total amount and history of waste are managed, and statistical information is provided. This system is continuously be operated and developed to oversee life-cycle information, and serve as the foundational database for the Waste Certification Program (WCP).

Domestic commercial low- and intermediate-level radioactive waste storage containers are manufactured using 1.2 mm thick cold-rolled steel sheets, and the outer surface is coated with a thin layer of primer of 10~36 μm. However, the outer surface of the primer of the container may be damaged due to physical friction, such as acceleration, resonance, and vibration during transportation. As a result, exposed steel surfaces undergo accelerated corrosion, reducing the overall durability of the container. The integrity of storage containers is directly related to the safety of workers. Therefore, the development of storage containers with enhanced durability is necessary. This paper provides an analysis of mechanical properties related to the durability of WC (tungsten carbide)-based coating materials for developing low- and intermediate-level radioactive waste storage containers. Three different WC-based coating specimens with varied composition ratios were prepared using HVOF (high-velocity oxy-fuel) technique. These different specimens (namely WC-85, WC-73, and WC-66) were uniformly deposited on cold-rolled steel surfaces ensuring a constant thickness of 250 μm. In this work, the mechanical properties of the three different WCbased coaitng materials evaluated from the viewpoints of microstructure, hardness, adheision force between substrate and coating material, and wear resistance. The cross-sectional SEM-EDS (Scanning Electron Microscope-Energy Dispersive X-ray Spectroscopy) images revealed that elements W (tungsten), C (carbon), Ni (nickel), and Cr (chromium) were uniformly distributed within the each coating layers which was approximately 250 μm thick. The average hardness values of HWC-85 and HWC-73 were found to be 1,091 Hv (Vickers Hardness) and 1,083 Hv, respectively, while the HWC-66 exhibited relatively lower hardness value of 883 Hv. This indicates that a higher WC content results in increased hardness. Adhesion force between and substrates and coating materials exceeded 60 MPa for all specimens, however, there were no significant differences observed based on the tungsten carbide content. Furthermore, a taber-type abrasion tester was used for conducting abrasion resistance tests under specific conditions including an H-18 load weight at 1,000 g with rotational speed set at 60 RPM. The abrasion resistance tests were performed under ambient temperatures (RT: 23±2°C) as well as relative humidity levels (RH: 50±10%). Currently, the ongoing abrasion resistance tests will include some results in this study.

As the acceptance criteria for low-intermediate-level radioactive waste cave disposal facilities of Korea Radioactive Waste Agency (KORAD) were revised, the requirements for characterization of whether radioactive waste contains hazardous substances have been strengthened. In addition, As the recent the Nuclear Safety and Security Commission Notice (Regulations on Delivery of Low- Medium-Level Radioactive Waste) scheduled to be revised, the management targets and standards for hazardous substances are scheduled to be specified and detailed. Accordingly, the Korea Atomic Energy Research Institute (KAERI) needs to prepare management methods and procedures for hazardous substances. In particular, in order to characterize the chemical requirements (explosiveness, ignitability, flammability, corrosiveness, and toxicity) contained in radioactive waste, it must be proven through documents or data that each item does not contain hazardous substances, and quality assurance for the overall process must be provided. In order to identify the characteristics of radioactive waste that will continue to be generated in the future, KAERI needs to introduce a management system for hazardous substances in radioactive waste and establish a quality assurance system. Currently, KAERI is thoroughly managing chelates (EDTA, NTA, etc.), but the detailed management procedures for hazardous substances related to chemical requirements in radioactive waste in the radiation management area specified above are insufficient. The KAERI’s Laboratory Safety Information Network has a total periodic regulatory review system in place for the purchase, movement, and disposal of chemical substances for each facility. However, there is no documents or data to prove that the hazardous substances held in the facility are not included in the radioactive waste, and there are no procedures for managing hazardous substances. Therefore, it is necessary to establish procedures for the management of hazardous substances, and we plan to prepare management procedures for hazardous substances so that chemical substances can be managed according to the procedures at each facility during preliminary inspection before receiving radioactive waste. The procedure provides definitions of terms and types of management targets for each characteristic of the chemical requirements specified above (explosiveness, ignition, flammability, corrosiveness, and toxicity). In addition, procedure also contains treatment methods of radioactive waste generated by using hazardous substances and management methods of in/out, quantity, history of that substances, etc. As the law is revised in the future, management will be carried out according to the relevant procedures. In this study, we aim to present the hazardous substance management procedures being established to determine whether radioactive waste contains hazardous substances in accordance with the revised the notice and strengthened acceptance criteria. Through this, we hope to contribute to improving reliability so that radioactive waste could be disposed of thoroughly and safely.

Once decommissioning begins, it is expected that large amount of radioactive wastes will be produced in a short period of time. The expected amount of radioactive wastes from Kori unit 1 NPP are approximately 80,000 drums (base on 200 L). By minimizing the amount of radioactive wastes generated through decontamination and reduction, KHNP has set the final target for the amount of radioactive wastes to be delivered to the disposal site at approximately 14,500 drums. Here, plasma torch melting technology is an essential technology for radioactive wastes treatment during nuclear power plants decommissioning and operation, because of its large volume reduction effects and the diversity of disposable wastes. KEPCO KPS was able to secure experience in operating Plasma Torch Melter (PTM) by conducting a research service for ‘development of plasma torch melting system advancement technology’ at KHNP-CRI. This study will compare kilo and Mega-Watt class PTM, largely categorized into facility configurations, operating parameters, and waste treatment. Based on this study, it would be desirable to operate PTM with approximate capacity according to the frequency and amount of waste production, and suggest volume for a kilo and Mega-watt class plasma torch in the melting furnace respectively. This plays to its strengths for both a kilo and Mega-watt class PTM.

A disposal of radioactive wastes is one of the urgent issues in worldwide. Considering upcoming plans for decommissioning of nuclear power plants, this problem is unavoidable and should be discussed very thoughtfully before long. There are variety of methods to deal with radioactive wastes, including Incineration process, conventional gasification process and plasma gasification process and so on. Among them, plasma gasification process is in the limelight due to its ecofriendly features and very large volume reduction effects. So, lots of countries like Japan, Taiwan, Russia, Bulgaria are already utilizing commercial plasma melting facilities and researching their own characteristics & disposal abilities and so on. Within the scope of this paper, I would like to introduce other countries current status of plasma melting facilities, and reach the conclusion on the directions to go for realistic radioactive wastes treatment.

In light of recent significant seismic events in Korea and worldwide, there is an urgent need to reevaluate the adequacy of seismic assessments conducted during facility construction. This study reexamines the ongoing viability of the Safety Shutdown Earthquake (SSE) criteria assessment for the Combustible Radioactive Waste Treatment Facility (CRWTF) site at the Korea Atomic Energy Research Institute (KAERI), originally established in 1994. To validate the SSE assessment, we delineated 13 seismic structure zones within the Korean Peninsula and employed two distinct methodologies. Initially, we updated earthquake occurrence data from 1994 to the present year (2023) to assess changes in the site’s horizontal maximum earthquake acceleration (g). Subsequently, we conducted a comparative analysis using the same dataset, contrasting the outcomes derived from the existing distance attenuation equation with those from the most recent attenuation equations to evaluate the reliability of the applied attenuation model. The Safety Shutdown Earthquake (SSE) criterion of 0.2 g remains unexceeded, even when considering recent earthquake events since the original evaluation in 1994. Furthermore, when applying various assessment equations developed subsequently, the maximum value obtained from the previously utilized ‘Donvan and Bornstein’ attenuation equation is 0.1496 g, closely resembling the outcome derived from the recently employed ‘Lee’ reduction equation of 0.1451 g. The SSE criteria for CRWTF remain valid in the current context, even in light of recent seismic occurrences such as the 2016 Gyeongju earthquake. Additionally, the attenuation equation employed in the evaluation consistently yields conservative results when compared to methodologies used in recent assessments. Consequently, the existing SSE criteria remain valid at present. This study is expected to serve as a valuable reference for confirming the SSE criterion assessment of similarly constructed facilities within KAERI.

Various radioactive metal wastes are generated during operation and decommissioning of nuclear facilities. Radioactive metal wastes with complex geometries or volumetric contamination can be difficult to decontaminate and disposal costs may increase. To solve these problems, the radioactive metal wastes can be treated by melting method. In this study, we designed a melting furnace system of air induction melting type, which is widely utilized due to its advantages of good thermal efficiency, uniform heating and guaranteed safety for radioactive material. By utilizing the melting furnace system, volatile radionuclides existed in the base material can be captured in the form of gas or dust by the filter. The radionuclides whose chemical properties can easily form metal oxides present as slag. For this reason, the specific radioactivity of the base material can be reduced. Radionuclides that are difficult to transport to slag and dust are uniformly distributed in the base material. A dedicated power supply and a transformer were necessary to be included in the melting furnace system since the induction furnace uses high-frequency currents. In addition, a hood is placed on top of the furnace to capture fumes generated during melting, and additional hoods were installed around the furnace to remove airborne dust. In particular, a dust collection unit consisting of a cyclone and a HEPA filter were constructed to effectively collect dust containing radionuclides. During the melting process, the slag is removed and accumulated separately, and the ingot production system was designed to produce the ingot using molten metal. The furnace was constructed for tilting the molten metal by moving the furnace using hydraulic system. The water cooling system and cooling tower were prepared to cool off the equipment with high temperature during melting is cooled off. The above process was specified in the operating procedure developed for this melting furnace system, and the operator shall operate and inspect according to the prescribed procedures. The radioactivity concentration in the sample taken in the step of tilting shall be analyzed whether they meet clearance level for self-disposal determined and publicly announced by the Commission. We can conduct self-disposal for the product of melting furnace system confirmed by the Commission as having the radioactivity concentration by nuclide not exceeding the value determined by the Commission.

The radioactive waste generated within radiation-controlled areas is classified and processed according to relevant laws and regulations based on contamination levels. In cases where such radioactive waste complies with the legally defined clearance concentration or dose criteria, it is disposed of as non-radioactive waste by means of incineration, reclamation, recycling, etc. Within radiation controlled areas, various consumables are periodically replaced to ensure the proper operation of the area. It is necessary to have appropriate disposal methods for these consumables. In particular, waste items such as fire extinguishers, fluorescent lamps, batteries, and pressure vessels (hereinafter referred to as “Special Waste Type”), which may contain hazardous substances within their internal components and contents, should be considered for appropriate disposal methods that comply with nuclear safety and environmental laws. In the present case, the specified special waste type do not come into direct contact with radiation sources, and they have impermeable surfaces, which significantly reduces the risk of external contamination infiltrating the interior. However, the current method of clearance is not suitable for these items (Typically, nuclear energy-related business operators are required to classify clearance target waste based on internal and external components and demonstrate compliance with the criteria. Nevertheless, for special waste type, it is difficult to separate and measure internal and external components within the radiation-controlled area). In this case, the Clearance Procedure for special waste type applied to Korea Atomic Energy Research Institute was introduced. Additionally, we have extracted considerations for future domestic clearance of the type.

Radioactive liquid waste generated during the operation of domestic nuclear power plants is treated through a somewhat different liquid radwaste system (LRS) for each plant. Prior to the introduction of standard nuclear power plants, LRS used a concentrated water dry system (CWDS) to evaporate liquid waste and manage it in the form of dry powder. The boron-containing radioactive liquid waste dry powder was solidified using paraffin from 1995 to 2010, and about 3,650 drums (based on 200 L) of paraffin solidified drums are currently stored in nuclear power plants. Paraffin solidification drums do not meet the acceptance criteria for radioactive waste repositories because it is difficult to secure the homogeneity of the solidified body and there are concerns about leaching of radioactive waste due to the low melting point of paraffin. In order to solve this problem and safely permanently dispose of paraffin solidification drums, the characteristics of dry powder paraffin solidification drums containing boron-containing radioactive liquid waste must be analyzed and appropriate treatment technology utilizing the results must be introduced. This study analyzes the physical properties of paraffin, the chemical properties of boron-containing radioactive waste dry powder, and the physicochemical properties of paraffin solidification powder, and proposes an appropriate alternative technology for treating boron-containing radioactive waste dry drum. When disposing of the paraffin solidification drum with boron-containing radioactive liquid waste dry powder, the solidification body must be effectively withdrawn from the drum and the paraffin must be completely separated from the solidification body. When disposing the drum, the solidified material must be effectively extracted from the drum and the paraffin must be completely separated from the solidified material. Afterwards, the paraffin must be self-disposed, and the radioactive waste must be disposed of in accordance with acceptance criteria of repository. We looked at how each characteristic of the paraffin solidification drum with boron-containing radioactive liquid waste dry powder can be utilized in each of the above treatment processes.

The decommissioning of Korea Research Reactor Units 1 and 2 (KRR 1&2), the first research reactors in South Korea, began in 1997 and the decommissioning status is currently proceeding with phase 3. It is expected that more than 5,000 tons of dismantled wastes will be generated as the contaminated building is demolished. Since these dismantled wastes must be disposed of in an efficient method considering economic feasibility, it is desirable to clearance extremely low-level wastes whose contamination is so minimal that the radiological risk is negligible. In Korea, in order to approve the clearance of radioactive waste, it must be proven that the nuclide concentration standards are met or that the dose to individuals and collectives is below the allowable dose value. At the KRR 1&2 decommissioning site, dismantled wastes have been steadily being disposed of through clearance procedure since 2021. Clearance was approved by the Korean Institute of Nuclear Safety (KINS) for one case of concrete waste in 2021 and two cases of metal waste in 2022. In 2023, the clearance of metal waste and asbestos waste has been approved so far, and in particular, this is the first case in Korea for asbestos waste. In this study, we compared the dose assessment methods and results of clearance wastes at the KRR 1&2 decommissioning site from 2021 to present. Dose assessment was conducted by applying the landfill scenario for concrete and asbestos and the recycling scenario for metal waste. The calculation codes used were RESRAD-onsite 7.2 and RESRAD-recycle 3.10. The dose conversion factors (DCF) for each age group (infant, 1y, 5y, 10y, 15y, adult) of the target nuclide used the values presented in ICRP-72, and in particular, geo-hydrological data of the actual landfill site was used as an input factor when evaluating landfill scenarios. As a result of the dose assessment, when landfilling concrete wastes in 2020, the personal dose and collective dose were evaluated the most at 2.80E+00 μSv/y and 4.83E-02 man·Sv/y, respectively.

Spent ion exchange resins have been generated during the operation of nuclear facilities. These resins include radioactive nuclides. It is needed to fabricate them into a stable form for final disposal. Cement solidification process is a useful method for the fabrication of them into a waste form for final disposal. In this study, proper conditions for the fabrication of them into a stable waste form were determined using the cement solidification process. In-drum waste forms were then produced at the conditions, where the stability of representative samples was evaluated for final disposal. The samples were satisfied to the Waste Acceptance Criteria for low and intermediate level radioactive waste disposal sites. This result can be utilized to derive optimal conditions for the fabrication of spent ion exchange resins into a final disposal form.

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.

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.

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.

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 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.

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.