This study presents a rapid and sequential radiochemical separation method for Pu and Am isotopes in radioactive waste samples from the nuclear power plant with anion exchange resin and TRU resin. After radionuclides were leached from the radioactive waste samples with concentrated HCl and HNO3, the sample was allowed to evaporate to dryness after filtering the leaching solution with 0.45 micron filter. The Pu isotopes were separated in HNO3 medium with anion exchange resin. For leaching solution passed through anion exchange column, the Am isotopes were separated with TRU resin. The purified Pu and Am isotopes were measured by alpha spectrometer, respectively, after micro-precipitation of neodymium. The sequential radiochemical separation of Pu and Am isotopes in radioactive waste samples using anion exchange resin and TRU resin was validated with ICP-MS system.

In this study, we introduce the validation of the analysis guidelines through preliminary experiments of the draft analysis guidelines before analyzing waste materials (non-combustible). This validation data was applied the accuracy and efficiency of the separation and analysis for the waste such as steel generated from NPP. Steel (non-flammable) was leached the mixed acid and the leaching solution was separated by using the separation guidelines. Steel was corroded with radioactive RM (Co-60, Cs-137) and mixed acid. After drying, the corroded steel was measured the initial radioactivity by a HPGe detector (10,000 seconds). The sample was inserted in a beaker and leached with mixed acid (10 M HNO3 + 4 M HCl) for 2 hours. In this solution, it added 2 ml of H2O2 to increase the leaching effect. The ultrasonic device was adjusted so that the temperature does not exceed 60°C. After elution, the surface of the sample was washed with pure water. The weight of the sample was measured accurately, and recorded the weight loss rate after infiltration. The leaching sample was measured radioactivity by a HPGe detector (10,000 seconds). It was calculated the recovery rate based on the difference in total radioactivity before and after leaching. Before the test, radioactive RM (Co-60, Cs-137) was radioactive deposited by corrosion, but Cs- 137 was not detected in the initial gamma measurement and only Co-60 nuclides were deposited. The recovery rate test results were confirmed to be about 100%.

Currently, non-volatile nuclides such as 94Nb, 99Tc, 90Sr, 55Fe, and 59/63Ni are used a sequential separation. In this study, we developed a separation for 99Tc and 90Sr by a carbonate precipitation. Sodium Carbonate (Na2CO3) was inserted in the aqueous sample from a Dry Active Waste (DAW) and a carbonate precipitation was produced. The precipitate is composed of di- or tri-valent element such as Co, Sr, Fe, Ni and the supernatant is composed of mono-valent element (Cs) and anion materials (ReO4 -, TcO4 -). In DAW, it was confirmed that the recovery of 90Sr (precipitate) and 99Tc (supernatant) were > 90%, respectively. The precipitate and supernatant separated by using a Sr-resin and an anion-exchange resin, respectively. The separated samples were measured by a Liquide Scintillation Counter (LSC, 90Sr) and Induced-Coupled Plasma-Mass Spectroscopy (ICPMS, 99Tc).

I-129 is one of the imporant nuclides that must be determined in the disposal process of radioactive waste in many countries. This radionuclide emits gamma-ray and x-ray photons within the energy range of 29 to 39 keV, consequently, an x-ray detector with high resolution performance is required for the analysis of I-129 activity. An n-type coaxial HPGe detector exhibits higher efficiency characteristics compared to a planar-type HPGe detector, however, its resolution is lower than a planar type. So it is difficult to completely deconvolute and fit the gamma-ray and xray peaks in the spectrum using a general gamma-ray spectrum analysis program such as GammaVision. To address this problem, in a previous study introduced the developed algorithm for the fitting and analysis of I-129 gamma-ray and x-ray spectum by fixing their emission ratios. In this study, we improved the algorithm by considering the variation of the efficiency in the HPGe spectrum, which reflects the actual HPGe crystal condition. And algorithm tests were performed using measured I-129 sample spectra with interfering nuclides acting as background curve are introduced.

Chelating agents, such as ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTPA), and nitrilotriacetic acid (NTA) are widely used in industry and agriculture as water softeners, detergents, and metal chelating agents. In wastewater treatment plants, a significant amount of chelating agents can be discharged into natural waters because they are difficult to degrade. Since those compounds affect the mobility of radionuclides or heavy metals in decontamination operations at nuclear facilities and radioactive waste disposal, quantification of the amount of ligand is very important for safe nuclear waste management. To predict the behavior of the main complexation in sample matrices of radioactive wastes, it is essential to evaluate the distribution of the metal-chelating species and their stabilities in order to develop analytical techniques for quantifying chelating agents. We have investigated to collect information on the pH speciation of metal chelation and the stability constants of metal complexes depending on three chelating agents (EDTA, DTPA, and NTA). For example, Zhang’s group recently reported that the initial coordination pH of Cu(II) and EDTA4− is delayed with the addition of Fe(III), and the pH range for the stable existence of [Cu(EDTA)]2− is narrowed compared to when it is alone in the sample matrix. The addition of Fe(III) clearly impacts the chemical states of the Cu(II)-EDTA solution. Additionally, Eivazihollagh’s group demonstrated differences in the speciation and stability of Cu(II) species between Cu(II) and three chelating ligands (EDTA, DTPA, and NTA). This study will be greatly helpful in identifying the sample matrix for binding major chelating agents and metals as well as developing chemically sample pretreatment and separation methods based on the sample matrix. Finally, these advancements will enable reliable quantitative analysis of chelating agents in decommissioning radioactive wastes.

Radiation from spent nuclear fuel (SNF) is one of key factors affecting the dissolution process of SNF and the source term from repository. The dissolution rate of uranium dioxide (UO2) matrix of SNF is expected to control the release of radionuclides from SNF in contact with water under geological disposal conditions. Based on the oxidative dissolution mechanism, the solubility of UO2 can increase significantly if the reducing environment near the fuel surface is altered by water radiolysis caused by radiation from SNF. Therefore, the analysis of water radiolysis products such as radicals (·OH, ·OH2, eaq, ·H) and molecules (H3O+, H2, H2O2) is perquisite for studies on the rate of such dissolution process to determine oxidation/dissolution mechanism and related rate constants. In this study we examined the two-known spectroscopic methods developed for H2O2 determination; one is the luminol-based chemiluminescence (luminol-CL) method and the other is the spectrophotometry using ferrous oxidation-xylenol orange complexation (FOX). Their applicability for quantitative analysis of H2O2 in potential aqueous samples from SNF dissolution studies was evaluated in terms of the analytical dynamic range (ADR), the limit of detection (LOD) and the interfering effects of various metal ions possibly present in real samples. The luminol-CL method exploits the chemiluminescence reaction caused by luminol; when in the presence of a metallic catalyst (e.g., Cu2+, Co2+), luminol emits a blue light (425 nm) at pH 10- 11 in response to oxidizing agents such as hydrogen peroxide. Although a flow-through reaction system is routinely employed to enhance the analytical sensitivity we achieved the ADR up to ~200 μM and LOD < 1 μM by a batch-wise CL detection using conventional cuvette cells and an intensified charge-coupled device (ICCD). Interestingly, it turned out that the interfering effects of other metal ions (e.g., UO2 2+, U4+, Fe2+ and Fe3+) is minimal, which should be advantageous for the luminol-CL method to be employed for samples potentially containing other metal ions. On the other hand, the FOX method spectrophotometrically analyzes H2O2 based on the difference in color (or absorption spectra) of Fe-xylenol orange (XO) complexes. Initially, the Fe2+-XO complex was provided in working solutions at pH 3, which was subsequently mixed with samples having H2O2 and allowed for quantitative oxidation of Fe2+ to Fe3+. Typically, by monitoring the absorbance of Fe3+-XO complex at 560-580 nm (λmax) the ADR up to ~100 μM and LOD ~1.6 μM were achieved. However, it is found that interfering effects from M3+ and M4+ ions are significant; these interfering metal ions can form XO complexes so as to directly contribute the measured absorbance. In contrast, the influence from M2+ ions was found to be negligible. To summarize we conclude that both methods can be applied for H2O2 determination for aqueous samples taken from SNF dissolution tests. However, prior to applying the FOX method the metal ion composition in those samples should be thoroughly identified not to overestimate the H2O2 concentration of samples. More details of underlying chemical reactions in both methods will be discussed in the presentation.

The radioactive contamination in the ocean has raised significant concern on the environmental impact among Asian and Pacific countries since the Fukushima Daiichi Nuclear Power Plant accident (Mar 11, 2011). The first step in determining the contamination by the radioactive material is monitoring anomalies of environmental radioactivity of interest. As a result, each country has its own environmental radioactivity surveillance program. Strontium-90 (half-life 28.8 y) is one of the radionuclides of high interest in the environment, owing to its high fission production rate and biological accumulation resulting from similar chemical behavior with calcium. The level of Strontium-90 in the seawater is very low, with a global average of about 1 mBq kg-1. Consequently, it requires large volume of seawater sample, typically ranging from 40 L to 60 L. The purification of 90Sr from seawater sample is challenging due to the high salinity and presence of stable Sr (about 7 ppm). Therefore, the conventional method for determining 90Sr is time-consuming and labor-intensive work. The author reported an advanced method, which is a more analyst-friendly and simpler method compared to the current method, for the determination of 90Sr in seawater. This method focuses on the separation of 90Y, which is equilibrium with 90Sr, utilizing a commercialized extraction resin. As a result, it takes less than 3 hours to determine 90Sr in 50 L of seawater sample and requires less labor. Additionally, this approach could be applied to the analysis of 90Sr in radioactive waste

The first commercial operation of Kori-1, which commenced in April 1978, was permanently shut down in June 2017, with plans for immediate dismantling. The decommissioning process of nuclear power plants generates a substantial amount of radioactive waste and poses significant radiation exposure risks to workers. Radioactivity is widely distributed throughout the primary coolant system of the reactor, including the reactor pressure vessel (RPV), steam generator (SG), and pressurizer. In particular, the SG has a considerable size and complex geometry, weighing approximately 326 tons and having a volume of 400 m3. The SG tubes are known to contain high levels of radioactivity, leading to significant radiation exposure to workers during the dismantling process. Therefore, this study aims to evaluate the workers’ radiation exposure during the cutting of SG tubes, which account for approximately 95% of the total radiation dose in the SG. Firstly, the CRUDTRAN code, developed to predict the behavior of soluble and particulate corrosion products in a PWR primary coolant system, is used to estimate the radioactive inventory in the SG tubes. Based on decontamination factors (DF) obtained in the SG tubes through overseas experience, the expected reduction in radioactivity during the Kori-1 reactor’s full-system decontamination (FSD) process is considered in the CRUDTRAN results. These results are then processed to estimate the radioactivity in both the straight and bent sections of the tubes. Subsequently, these radioactivity values are used as inputs for the MicroShield code to calculate the worker radiation exposure during the cutting of both straight and bent sections of the tubes. The cutting process assumes that each SG tube section is cut in a separate, shielded area, and the radiation exposure is assessed, taking into account factors such as cutting equipment, cutting length, working hours, and working distance. This study evaluates the worker radiation exposure during the cutting of SG tubes, which are expected to have a significantly high radioactivity due to chalk river unidentified deposit (CRUD). This assessment also considers the reduction in radioactivity within the steam generator tubes resulting from the FSD process. Consequently, it enables an examination of how worker radiation exposure varies based on the extent of FSD. This study may provide valuable insights for determining the scope and extent of the FSD process and the development of shielding methods during the dismantling of SG tubes in the future.

The dismantling nuclear power plant is expected to continue to change the radiation working environment compared to the operating nuclear power plant. Contamination monitors and survey meters currently in use have limitations in accurate analysis source term and dose rates for continuous changes in radiation fields at dismantling sites. Due to these limitations, the use of semiconductor detectors such as HPGe and CZT detectors with excellent energy resolution and portability is increasing. The CZT detector performs as well as the HPGe detector, but there is no proven calibration procedure yet. Therefore, in this study, the HPGe calibration method was reviewed to derive implications for the CZT detector calibration method. The operating principle of a semiconductor detector that measures gamma emission energy converts them into electrical signals is the same. Two calibrations of HPGe detectors are performed according to the standard calibration procedure for semiconductor detectors for gamma-ray measurement issued by the Korea Association of Standards & Testing Organizations. The first is an energy calibration that calculates gamma-ray peak position measurements and relational expressions using standard source term that emit gamma-rays. The channel values for energy are measured using certified reference source term to determine radionuclides by identifying channels corresponding to the measured peak energy values. The second is the measurement efficiency of measuring the coefficient calibration device, which measures gamma rays emitted from the standard source term. The detector efficiency by sample or distance is measured in consideration of the shape, size, volume, and density of the calibration device. The HPGe detector performs calibration once every six months through a verified calibration method and is being used as a source term analyzer at the power plant. The CZT detector may also establish a procedure for identifying peak positions through energy calibration and calculating radioactivity through efficiency calibration. This will be a way to expand the usability of semiconductor detectors and further monitor radiation in a more effective way.

South Korea’s first commercial nuclear reactor, Kori Unit 1, was permanently shut down in 2017, and preparations are currently underway for its decommissioning. After the permanent shutdown, the spent nuclear fuel from the reactor core is removed and stored in a spent fuel storage facility. Subsequently, steps are taken for its permanent disposal, and if a permanent disposal site is not determined, it is stored in an interim storage facility (or temporary storage facility). Therefore, the activation criteria for radiation emergency plans vary depending on the movement of spent nuclear fuel and the storage location. In this study, it reviewed emergency plans in the U.S. NRC Regulatory Guide (Draft) titled ‘Emergency Planning for Decommissioning Nuclear Power Reactors’ to determine the requirements for radiation emergency plans needed for decommissioned nuclear power plants. Additionally, by examining emergency plans applied to decommissioning nuclear power plants in the United States, this study identified emergency plan requirement that could be applicable to future decommissioned nuclear power plants in South Korea. This study will contribute to the establishment of appropriate radiation emergency plans for decommissioning nuclear power plants in Korea for providing accurate information on overseas cases and relevant guidelines.

Radiation workers, especially those dealing with Uranium isotopes, can potentially intake Uranium -containing materials through their respiratory and digestive systems. According to the “Regulations on the Measurement and Calculation of Internal Exposure” from Nuclear Safety and Security Commission (NSSC), those who intend to work in or enter the nuclear facilities with a risk of exceeding 2 mSv exposure per year should be examined the internal exposure. However, when it comes to in-vitro bioassay, Uranium intake through drinking water can affect the quantitative analysis. The International Commission on Radiological Protection (ICRP) reported in ICRP Publication 23 (Report on the Task Group on Reference Man) that the reference man excretes Uranium in the urine (0.05-0.5 μg/day) and feces (1.4-1.8 μg/day). Korea Atomic Energy Research Institute (KAERI) set the 90.5 ng/day as the 238U background of workers handing Uranium based on the daily Uranium intake of Koreans. In this research, we examined the possible effects of Uranium in drinking water on internal exposure by analyzing the concentration of Uranium in bottled waters from various water sources sold in the domestic market and a water from the water purifier. The 238U concentration results of analyzing 11 bottled waters and 1 purified water, were ranged from 0 to 10.2 μg/L. All the results were satisfied the standard of 30 μg/L according to “Regulations for Drinking Water Quality Standards and Inspection” enacted by the Ministry of Environment. However, various concentrations were shown depending on the water sources. Assuming that these concentrations of water are consumed by drinking 1 L per day, the internal dose assessment result is 0 to 0.94 mSv. On the other hand, if it is assumed to be inhaled, it can be an overestimated because the dose coefficient of inhalation, Type M is higher than that of ingestion, f1=0.02 which are the values recommended by ICRP Publication 78 (Individual Monitoring for Internal Exposure of Workers) when the Uranium compound is unspecified. In case of two workers at KAERI, the daily excretion of urine was 151 and 120 ng/day respectively in the first quarter monitoring. However after changing the kind of drinking water in the second quarter monitoring, it dropped to 17.4 and 15.4 ng/day respectively. Through this study, it is confirmed that the Uranium background in urine can be analyzed differently depending on the kind of drinking water consumed by each worker. Depending on the Uranium concentration of drinking water, the internal exposure dose assessment can be overestimated or underestimated. Therefore, the Uranium concentration and intake amount according to the kind of drinking water should be considered for in-vitro bioassays of Uranium handlers. Furthermore, if necessary, the Uranium isotope ratio analysis in urine and the handling information should be comprehensively considered. In addition, in order to exclude the effect of intake through the digestive system, replacing the kind of drinking water can be considered. The additional analysis such as in-vivo bioassay and 24 hours urine analysis rather than spot samples can be also recommended.

The operation of nuclear facilities involves the potential for on-site contamination of soil, primarily resulting from pipe leaks and other operational incidents. Globally, decommissioning process for commercial nuclear power plants have revealed huge-amounts of soil waste contaminated with Cs-137, Sr-90, Co-60, and H-3. For example, Connecticut Yankee in the United States produced approximately 52,800 ton of contaminated soil waste, constituting 10% of the total waste generated during its decommissioning. Environmental remediation costs associated with nuclear decommissioning in the US averaged $60 million per unit, representing a significant 10% of the whole decommissioning expenses. Consequently, this study undertook a preliminary investigation to identify important factors for establishing a site remediation strategy based on radionuclide- and site-specific media- characteristics, focusing the efficiency enhancement for the environmental remediation. The factors considered for this investigation were categorized into physical/environmental, socioeconomic, technical, and management aspects. Physical/environmental factors contained the site characteristics, contamination levels, and environmental sensitivity, while socio-economic factors included the social concerns and economic costs. Technical and management factors included subcategories such as technical considerations, policy aspects, and management factors. Especially, technical factors were further subdivided to consider the site reuse potential, secondary waste generation by site remediation, remediation efficiency, and remediation time. Additionally, our study focused the key factors that facilitate the systematic planning for the site remediation, considering the distribution coefficient (Kd) and hydrogeological characteristics associated with each radionuclide in specific site conditions. Therefore, key factors in this study focus the geochemical characteristics of site media including the particle size distribution, chemical composition, organic and inorganic constituents, and soil moisture content. Moreover, the adsorption properties of site media were examined concerning the distribution coefficient (Kd) of radionuclides and their migration characteristics. Furthermore, this study supported the development of a conceptual framework, containing the remediation strategies that incorporate the mobility of radionuclides, according to the site-specific media. This conceptual framework would necessitate the spatial analysis techniques involving the whole contamination surveys and radionuclide mobility modeling data. By integrating these key factors, the study provides the selection and simulation of optimal remediation methods, ultimately offering the estimated amounts of radioactive waste and its disposal costs. Therefore, these key factors offer foundational insights for designing the site remediation strategies according the sitespecific information such as the distribution coefficient (Kd) and hydrogeological characteristics.

KEPCO KPS is the contractor for the full system decontamination (FSD) of Kori Unit 1 and under preparation such as modification, lay out for equipment installation, setting up tie-in/out point for chemical injection and way to pressurize the system, of its successful performance. In this research, KPS introduced how KPS has designed and prepared for the FSD project and how will the chemical decontamination process be implemented. As described in the previous research, chemical decontamination process is planned to be conducted for three cycles and each cycle is consisted of oxidation, reduction, decomposition, and purification. Oxidation and reduction process were conducted at 90°C. Chemical decomposition and purification process were conducted at 40°C due to the damage of IX by the heat. If the decontamination result does not meet the target DF and the dose rate, additional cycle can be conducted. Expected volume of process water for FSD is 200 m3. Three systems have been designated as decontamination targets: reactor coolant system (RCS), residual heat removal system (RHRS), chemical volume control system (CVCS). For the steady flow rate, existed plant equipment such as reactor coolant pump (RCP) will be operated and modifications on some components will be conducted. Due to the limited space for installation, decontamination equipment and other resources are distributed to three different places. KPS designed the layout of equipment installed inside the containment vessel. The layout contains the information of shielding for highly radiated equipment such as IX and filter skid.

The thermal treatment of radioactive waste attracts great attention. The thermal treatment offers lots of advantages, such as significant volume reduction, hazard reduction, increase of disposal safety, etc. There are various thermal technologies to waste. The developed technologies are calcination, incineration, melting, molten salt oxidation, plasma, pyrolysis, synroc, vitrification, etc. The off-gas treatment system is widely applied in the technologies to increase the safety and operation efficiency. The thermal treatment generates various by-product and pollutants during the process. The dust or fly ash are generated as a particulate from almost every radioactive waste. The treatment of PVC related components generates hydrogen chloride, which usually brings corrosion of facility. The treatment of rubber and spent resin generates sulfur oxide, SOx. The treatment of nitrile rubber generates nitrogen oxide, NOx. The incomplete combustion of radioactive waste usually generates carbon oxide, COx. The process temperature also affects the generation of off gas, such as NOx and/or COx. Various off gas treatment components are organized for the proper treatment of the previously mentioned materials. In this study systematical review on off gas treatment will be reported. Also, worldwide experiences and developed facility will be reported.

The primary purpose of high temperature process of radioactive waste is to satisfy the waste acceptance criteria and volume reduction. The WAC offers the guideline of waste form fabrication process. The WAC is defined as quantitative or qualitative criteria specified by the regulatory body, or specified by and operator and approved by the regulatory body, for radioactive waste to be accepted by the operator of a repository for disposal, or by the operator of a storage facility for storage. The main objective of WAC is to protect staff and general public and environment by the containment of radioactive material, limit external radiation level, and prevent criticality. The WAC also offers systematic management of radioactive waste by standardization of waste management operations, facilitation waste tracking, ensure safe and effective operation of operating facilities, etc. Since the high temperature process for radioactive waste is considered in many countries, lots of codes and standards are considered. In many WACs, compressive strength, thermal cycle stability, radiation exposure stability, free liquid, and leachability are evaluation to understand the effect of solidified form to the disposal facility. In this paper, systematical review on waste form will be discussed. In addition, brief result of characterization of waste form will be compared.

In 2017, the permanent shutdown of Kori Unit 1 was decided, marking the initiation of preparations for the decontamination and decommissioning of Kori Unit 1. The dismantling of radiologically contaminated equipment and concrete structures such as the Reactor Vessel (RV), Reactor Vessel Internals (RVI), and the Bio shield is crucial in the nuclear decommissioning process. These components became radiologically contaminated due to nuclear fission reactions occurring in the reactor during its operational period. The RVI dismantling at Spain’s Jose Cabrera Nuclear Power Plant involved the use of mechanical saws and disk cutters to divide it into approximately 430 pieces, taking 16 months to complete. Germany’s Stade Nuclear Power Plant employed mechanical circular saws to segment their RVI into about 170 pieces, which took 30 months to accomplish. Meanwhile, the RVI at Germany’s Wurgassen Nuclear Power Plant was subdivided into approximately 1,200 pieces using a combination of mechanical saws and abrasive water jets, requiring 61 months for completion. Due to the radioactivity in Kori Unit 1’s Reactor Vessel (RV) and Reactor Vessel Internals (RVI), remote-controlled systems were developed for cutting within the cavity to reduce radiation exposure. Specialized equipment was developed for underwater cutting operations. This paper focuses on modeling related to RVI operations using the MAVRIC code. The upper and lower parts of the RVI are classified as low-level radioactive waste, while the sides of the RVI that come into contact with fuel are classified as intermediate-level radioactive waste. Therefore, the modeling presented in this paper only considers the RVI sides since the upper and lower parts have a minimal impact on radiation exposure. Accurate calculations were performed through geometric modeling and radiation dose modeling. These research findings are anticipated to contribute to enhancing the efficiency and safety of nuclear reactor decommissioning operations

In nuclear power plant (NPP) decommissioning, ventilation and purification of the building atmosphere are important to create a working environment, ensure worker safety, and prevent the release of gaseous radioactive materials into the environment. The heating, ventilation, and air conditioning (HVAC) system of each building is maintained, modified, or newly installed. In this study, based on APR1400, operation strategies were presented in case of ventilation abnormalities in the reactor containment building (RCB), where highly radioactive particles and high dust are most frequently generated during NPP decommissioning. For research, it was assumed that the entire RCB atmospheric ventilation during decommissioning would use the RCB purge system of the existing NPP and perform continuous ventilation. Additionally, it is assumed that areas where high radiation particles and high dust occur locally, such as reactor containers or internal segments, are sealed with tents and purified using a HEFA filter of a temporary portable HVAC, and a exhaust flow path is connected to the discharge duct of the existing RCB purge system. The possibility of abnormal occurrence was largely divided into two cases. First, when large amounts of uncontrolled pollutants are released into the atmosphere inside the RCB, discharge to the environment is stopped manually or automatically by a modified engineered safety function activation signal (ESFAS). Afterwards, the RCB purge system should be operated in recirculation mode to sufficiently purify the RCB atmosphere with a HEPA filter. Second, when the first train of the low volume purge system is not running due to a failure, standby train should be operated. If both low volume purge trains fail, a high volume purge system is used. Intermittent purge operation is preferred due to large capacity during high volume purge operation. In cases where it is not possible to operate all purge systems due to common issues such as power supply, atmospheric sampling is performed to determine whether to proceed with the work inside RCB.

Kori Unit 1, pressurized water reactor, is the Korea’s first commercial nuclear power plant. It successfully generated electricity for a period of 30 years, commencing from April 19, 1978. Following its approval for continued operation in 2008, Kori Unit 1 continued to operate for an additional 9 years, resulting in a total operational period of 39 years. On June 18, 2017, Kori Unit 1 was permanently shut down. Since then, Korea is actively preparing for the decommissioning of nuclear power plant. During the decommissioning of a nuclear power plant, the heavy components such as reactor, steam generator, pressurizer, reactor coolant pump located in the containment building should be taken out of the containment building. To take out heavy components from the containment building, pipes connected to heavy component should be cut. There are numerous pipes connected to the heavy component, each with varying dimensions and material. Each pipe has a different level of contamination depending on its use. In this study, optimal cutting method of pipe connected to steam generator, one of the heavy components of nuclear power plant, is proposed during the decommissioning of Kori unit 1. In case of pipe connected to Kori unit 1 steam generator, material is stainless steel or carbon steel. These pipes have varying inner diameter, ranging from 0.6 cm to 74 cm, and thickness ranging from 0.15 cm to 7.1 cm. These pipes are classified as low and intermediate level waste (LILW) or very low level waste (VLLW). Because characteristics of pipes are different, each pipe optimal cutting methods are proposed differently considering material, dimension, contamination level, cutting cost, cutting time, and the management of secondary waste. As a result, the cutting method for pipe of reactor coolant system is selected to orbital cutting. The cutting method of main steam pipe and main feedwater pipe is selected to oxygen cutting. In case of other small pipes, cutting method is selected to circular saw.

The radiological characterization of SSCs (Structure, Systems and Components) plays one of the most important role for the decommissioning of KORI Unit-1 during the preparation periods. Generally, a regulatory body and laws relating to the decommissioning focus on the separation and appropriate disposal or storage of radiological waste including ILW (intermediate level waste), LLW (low level waste), VLLW (very low level waste) and CW (clearance waste), aligned with their contamination characteristics. The result of the preliminary radiological characterization of KORI Unit-1 indicated that, apart from neutron activated the RV (reactor vessel), RVI (reactor vessel internals), and BS (biological shielding concrete), the majorities of contamination were sorted to be less than LLW. Radiological contamination can be evaluated into two methods. Due to the difficulties of directly measuring contamination on the interior surfaces of the pipe, called CRUD, the assessment was implemented by modeling method, that is measuring contamination on the exterior surfaces of the pipes and calculating relative factors such as thickness and size. This indirect method may be affected by the surrounding radiation distribution, and only a few gamma nuclides can be measured. Therefore, it has limitation in terms of providing detailed nuclide information. Especially, α and β nuclides can only be estimated roughly by scaling factors, comparing their relative ratios with the existing gamma results. To overcome the limitation of indirect measurement, a destructive sampling method has been employed to assess the contamination of the systems and component. Samples are physically taken some parts of the systems or components and subsequently analyzed in the laboratory to evaluate detailed nuclides and total contamination. For the characterization of KORI Unit-1, we conducted the radiation measurement on the exterior surfaces of components using portable instruments (Eberline E-600 SPA3, Thermo G20-10, Thermo G10, Thermo FH40TG) at BR (boron recycle system) and SP (containment spray system) in primary system. Based on these results, the ProUCL program was employed to determine the destructive sample collection quantities based on statistical approach. The total of 5 and 8 destructive sample quantities were decided by program and successfully collected from the BR and SP systems, respectively. Samples were moved to laboratory and analyzed for the detail nuclide characteristics. The outcomes of this study are expected to serve as valuable information for estimating the types and quantities of radiological waste generated by decommissioning of KORI Unit-1.

Korea Atomic Energy Research Institute (KAERI) has been operating the Post Irradiation Examination Facility (PIEF) for fuel examinations. The facility has pools and hot cells for handling and examining fuel assemblies and rods. Among the hot cells, the second cell is for measuring rod internal pressure (RIP) and then cutting the rod to make samples for destructive tests. Currently, the cutting machine is broken, so it has to be replaced. Because the existing cutting machine consists of many parts and its size was quite a bit large to handle and treat for the radioactive waste disposal, the disassembly work has been performed to make it smaller using manipulators. The drawings of the cutting machine were reviewed and the disassembly tools were developed considering workability when the work performed at the hot cell using the manipulators. The large parts such as motor, mirror and cable, etc., were able to be disassembled and the machine size became so smaller that it could be easily handled for the disposal.