For safe disposal of radioactive wastes, accurate analysis of nuclear isotopes is important. It is known that there are 14 nuclides that have to identify nuclide-specific concentration levels. 63Ni, one of non-volatile nuclear isotopes which is included in those 14 nuclides, has to follow chemical separation for exact analysis. As various analysis methods were developed, various methods for analyzing 63Ni also emerged. Past method has used measurement specimens of 59Ni, after 59Ni measurement has been done. It used HClO4, known as strong oxidizing agent, to dissolve DMG, an organic substance used to form 59Ni precipitates. Nowadays, we analyze 59Ni and 63Ni simultaneously, which enables short analysis time, without use of HClO4. But high accuracy is just as important as short measurement time and efficiency. So, this paper compare 63Ni specific activity value used new method with the value, past method used, using real sample’s data. As a result, all sample data from new method’s relative 63Ni specific activity is within the uncertainty range of past ones based on past specific activity value. Consistency of new method’s result and past method’s data increased the reliability of the data and accuracy of those methods.

Chelating agents in low and intermediate radioactive wastes can form complexes with radionuclides and increase the mobility of the radionuclides. According to the Korea Radioactive Waste Agency (Acceptance criteria for low and intermediate radioactive waste, WAC-SIL-2022-1), if the amount of residual chelating agents in the waste are greater than 0.1%, the chemical names and residual amounts should be specified; if greater than 1%, the waste must be solidified and contain no more than 8%. The existing method for analyzing chelates in radioactive waste was based on UV–Visible spectrophotometry (UV-Vis), but the new method is based on liquid chromatography/mass spectrometry (LC-MS). The analysis was performed in aqueous solution before applying to real samples. Since the real sample may contain several heavy metals, it is expected that the chelates will exist as complexes. Therefore, 1.0×10-4 mol L-1 of EDTA (Ethylenediaminetetraacetic acid), DTPA (Diethylenetriaminepentaacetic acid), NTA (Nitrilotriacetic acid), and excess metals in aqueous solution were analyzed using HPLC using RP (Reverse Phase) column and HILIC (Hydrophilic interaction) column. When the RP column was used, each substance eluted without separation at the beginning of the analysis. However, when analyzed using a HILIC column, the peaks of each substance were separated. LC-MS measurements using HILIC conditions resulted in separations with better sensitivity.

Concrete is the primary building material for nuclear facilities, making it one of the most common forms of radioactive waste generated when decommissioning a nuclear facility. Of the total waste generated at the Connecticut Yankee and Maine Yankee nuclear power plants in the United States, concrete waste accounts for 83.5% of the total for Connecticut Yankee and 52% for Maine Yankee. In order to dispose of the low- to medium-level radioactive concrete waste generated during the decommissioning of nuclear power plants, it is necessary to analyze the radioactivity concentration of gamma nuclides such as Co-58, Co-60, Cs-137, and Ce-144. Gamma-ray spectroscopy is commonly used method to measure the radioactivity concentration of gamma nuclides in the radioactive waste; however, due to the nature of gamma detectors, gamma rays from sequentially decaying nuclides such as Co-60 or Y-88 are subject to True Coincidence Summing (TCS). TCS reduces the Full Energy Peak Efficiency (FEPE) of specific gamma ray and it can cause underestimation of radioactivity concentration. Therefor the TCS effect must be compensated for in order to accurately assess the radioactivity of the sample. In addition, samples with high density and large volume will experience a certain level of self-shielding effect of gamma rays, so this must also be compensated for. The Radioactive Waste Chemical Analysis Center at the Korea Atomic Energy Research Institute performs nuclide analysis for the final disposal of low- and intermediate-level concrete waste. Since a large number of samples must be analyzed within the facility, the analytical method must simultaneously satisfy accuracy and speed. In this study, we report on the results of evaluating the accuracy of the radioactivity concentration correction by applying an efficiency transfer method that appears to satisfy these requirements to concrete standard reference material.

Alpha activities can be used for categorization, transportation, and disposal of radioactive waste generated from the operation of nuclear facilities including nuclear power plants. In order to transport and dispose of such low- and intermediate-level radioactive waste (LILW) to the Wolsong LILW Disposal Center (WLDC) at Gyeongju, the gross alpha concentration of an individual drum should be determined according to the acceptance criteria. In addition, when the gross alpha concentration exceeds 10 Bq/g, the inventory of the comprising alpha emitters in the waste is to be identified. Gross alpha measurements using a proportional counter are usually straightforward, inexpensive, and high-throughput, so they are broadly used to assay the total alpha activity for environmental, health physics, and emergency-response assessments. However, several factors are thoughtfully considered to obtain a reliable approximate for the entire alpha emitters in a sample, which include the alpha particle energy of a particular radionuclide, the radionuclide that is used as a calibration standard, the uniformity of film in a planchet, time between sample collection and sample preparation, and time between sample preparation and counting. Korea Atomic Energy Research Institute (KAERI) have evaluated the inventory of radionuclides in low-level radioactive waste drums to send every year hundreds of them to the WLDC. In this presentation, we revisit the gross alpha measurement results of the drums transported to WLDC in the past few years and compare them with the concentrations of alpha emitters measured from alpha spectrometry and gamma spectrometry. This study offers an insight into the gross alpha measurement for radioactive waste regarding calibration source, self-absorption effect, composition of alpha emitters, etc.

To achieve permanent disposal of radioactive waste drums, the radionuclides analysis process is essential. A variety of waste types are generated through the operation of nuclear facilities, with dry active waste (DAW) being the most abundant. To perform radionuclides analysis, sample pretreatment technology is required to transform solid samples into solutions. In this study, we developed a dry ashing-microwave digestion method and secured the reliability of the analysis results through a validity evaluation. Additionally, we conducted a comparative analysis of the radioactivity of 94Nb nuclides with and without the chemical separation process, which reduced the minimum detectable activity (MDA) level by more than 65-fold for a certain sample.

The radioactive cesium, released from the normal operation or the accidental operation of nuclear facilities, should be regularly monitored for environmental regulatory compliance. The 135Cs/137Cs isotopic ratios, potentially useful for long-term tracking Cs transport in seawater, can be used as a tool of understanding how radionuclides are transported from different nuclear production source terms and distributed in the ocean. The ultra-high sensitive mass spectrometers (TIMS, SF-ICP-MS and TQ-ICP-MS) have been used to measure the 135Cs/137Cs isotopic ratios. However, the radiochemical separation of Cs from the seawater matrix is essential for the analysis of Cs using the mass spectrometers. An automated radiochemical procedure for the separation of Cs in seawater was developed for the analysis of 135Cs/137Cs isotopic ratios using a sequential column chromatography with AMPPAN and AG50Wx8 cation exchange resins. National Instrument’s LabVIEW is a graphical programming language and a powerful tool for the instrument control. A virtual instrument system for the automated separation of cesium isotopes was developed by the state machine of the fundamental design patterns in LabVIEW. In this study, the conceptual designs of an automated separation system of cesium isotopes, its virtual instrument system based on the LabVIEW state machine architectures and an automated radiochemical procedure were described for the purification of cesium isotopes at trace levels found in seawater discharged from the various nuclear facilities.

To secure approval for a decommissioning plan in Korea, it is essential to evaluate contamination dispersion through groundwater during the decommissioning process. To achieve this, licensees must assess the groundwater characteristics of the facility’s site and subsequently develop a groundwater flow model. It is worth noting that Combustible Radioactive Waste Treatment Facility (CRWTF) is characterized by their simplicity and absence of liquid radioactive waste generation. Given these facility characteristics, the groundwater flow model for CRWTF utilizes data from neighboring facilities, with the feasibility of using reference data substantiated through comparative analysis involving groundwater characteristic testing and on-site modeling. To enable a comparison between the actual site’s groundwater characteristics and the referenced modeling, two types of hydraulic constant characterization tests were conducted. First, hydraulic conductivity was determined through long-term pumping and recovery tests. The ‘Theis’ and ‘Cooper-Jacob’ equations, along with the ‘Theis recovery’ equation, were applied to calculate hydraulic conductivity, and the final result adopted the average of the calculated values. Secondly, a groundwater flow test was conducted to confirm the alignment between the main flow direction of the referenced model and the groundwater flow in the CRWTF, utilizing the particle tracking technique. The evaluation of hydraulic conductivity from the hydraulic constant test revealed that the measured value at the actual site was approximately 1.84 times higher than the modeled value. This variance is considered valid, taking into consideration the modeling’s calibration range and the fact that measurements were taken during a period characterized by wet conditions. Furthermore, a close correspondence was observed between the groundwater flow direction in the reference model (ranging from 90° to 170°) and the facility’s actual flow direction (ranging from 78° to 95°). The results of reference data for the CRWTF, based on the nearby facility’s model, were validated through the hydraulic properties test. Consequently, the modeling data can be employed for the demolition plan of CRWTF. It is also anticipated that these comparative analysis methods will be instrumental in shaping the groundwater investigation plans for facilities with characteristics similar to CRWTF.

This study presents distribution of naturally occurring radioactive materials in groundwater in Jeju island. Radon (222Rn) and potassium (40K) concentrations were performed by using Liquid Scintillation Counter and Ion Chromatograph respectively. In addition, the activities of uranium and thorium nuclides were analyzed by Inductively Coupled Plasma Mass Spectroscopy. Groundwater samples were collected from 9 sites of water intake facilities for wide area supply in Jeju island from September 2022 to September 2023. The 40K concentrations of groundwater ranged between 0.050 and 0.400 Bq·L-1. The radon concentrations in groundwater were in the range of 0 to 60 Bq L-1, and there was no groundwater exceeding the range of 148 Bq L-1 proposed by the US EPA. The distribution of uranium and thorium in groundwater varied from 0 to 500 ng L-1 and 0 to 2.4 ng L-1, respectively. The concentrations of uranium did not exceed 30 μg L-1, thresholds indicated by the US EPA. By analyzing the concentrations of 40K, 222Rn, 238U and 232Th, the annual effective dose of residents can be assessed. The evaluated residents’ effective dose from natural radionuclides due to intake of drinking water is less than the recommended value of 100 μSv y-1. Consequently, this study indicates that the cancer risks of the residents in Jeju island from naturally occurring radioactive materials ingested with water is insignificant.

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.

Wet solid wastes including spent ion exchange resins, evaporator concentrates and sludges require solidification to transform wastes into an acceptable solid, monolithic form for final disposal. The development of the process control program for the solidification of radioactive sludges generated at nuclear power plants has been in progress to provide reasonable assurance that the solidified product will meet the established waste acceptance criteria for solidified waste. A mobile solidification system to produce the solidified waste in the size of a 200 L drum was used, which adopts the in-line mixing method where the waste and binder are mixed and then transferred to the disposable container. To simulate radioactive sludges, non-radioactive sludges are synthesized and the specimens are prepared by using them. The qualification tests on the prepared specimens including the compressive strength test, the thermal cycling test, the irradiation test, the leach test, the immersion test, etc. have been performed to qualify recipes for a range of waste compositions. The results of the tests will be analyzed and discussed.

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).

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.

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.

Dry active wastes (DAWs) are combustible waste generated during the operation and decommissioning of nuclear facilities, and are known to be generated in the amount of approximately 10,000 to 40,000 drums (based on 200 L) per unit. It consists of various types of protective clothing, paper, and plastic bags, and is stored in radioactive waste storage facilities. Therefore, reducing the volume of DAWs is an important issue in order to reduce storage costs and utilize the limited space of waste storage facilities. Heat treatment such as incineration can dramatically reduce the volume of waste, but as the waste is thermally decomposed, CO2, a global warming gas, is generated and there is a risk of emissions of harmful gases including radionuclides. Therefore, a heat treatment process that minimizes the generation of CO2 and harmful gases is necessary. One of the alternatives to incineration is to carbonize DAWs, dispose of carbonized materials below the release standard as non-radioactive waste, and selectively separate and stabilize inorganic components, including radionuclides, from carbonized DAWs. In this study, 13 types of DAWs generated from nuclear power plants were selected and their thermal decomposition characteristics were investigated to design a heat treatment process that replaces incineration. As a result of TGA analysis, the temperature at which thermal decomposition of each waste begins is 260-300°C for cotton, 320-330°C for paper, 315-420°C for synthetic fiber, 350°C for latex gloves. The mass of most samples decreased to less than 1 % of the initial weight after heat treatment, and dust suit and latex gloves had residues of 13.83% and 13.71% of the initial mass, respectively. The metal components of the residue produced after heat treatment of the sample were analyzed by EDS. According to the EDS results, cotton contains Ca and Al, paper contains Ca, Al and Si, synthetic fiber contains Ca, Cu and Ti, latex gloves contain Ca and Mg. Additionally, ICP analysis was performed to quantify the inorganic components. These results are expected to be applicable to the processing of DAW generated at nuclear facilities in the future.

Concentrated effluent and spent ion exchange resins (IERs) from nuclear power plants (NPPs) were generated prior to the establishment of a disposal facility site and waste acceptance criteria have been temporarily stored at the NPPs because their suitability for disposal has not been confirmed. In particular, at the Kori Unit 1, which was the first to start the commercial operation in South Korea, the initially generated concentrated effluent and IERs are repackaged in large size of concrete containers and stored without provided regulation standard. The concentrated effluent is package as cementitious form in 200 L drums and repackaged in concrete containers, case of the IERs were solidified or dehydrated and repackaged in round concrete container. In this study, we review and propose a disposal plan for concentrated effluent and IERs repackaging drums that have not been confirmed to be suitable for disposal from the first operating nuclear power plant, Kori Unit 1, 2. First, the concentrated effluent was stored in four 200 L drums respectively, and then, it was again stored in concrete container and which was poured on top using grouted concrete. Therefore, the process was required by cutting concrete container for extracting the internal drums at first. Internal radioactive waste should be crushed to the suitable waste criteria and solidified, finally disposal in to the polymer concrete high integrity container (PC-HIC). IER was repackaged and disposal in square type of 200 L concrete drums respectively covered the cap. So, extracting the internal drums should be extracted after removing the cap of external concrete container. Cement solidification drums can be crushed and re-solidified or disposed in the PC-HIC. Stored IER after dehydrated can be disposal in PC-HIC. In conclusion, the container was used as a package that repackaging the concentrated effluent and IER was separated into two different types of waste depending on the level of contamination of radioactivity, the polluted area is disposed of as radioactivity contamination or the unspoiled area will be treated as self-disposal waste.

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 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.

The mobility of uranium (U) in various disposal environments of a deep geological repository is controlled by various geochemical conditions and parameters. In particular, oxidation state of uranium is considered as a major factor to control the mobility of uranium in most of geological environments. In this study, therefore, we investigated the geochemical behaviors of uranium in grounwater samples from natural analogue study sites located in the Ogcheon Metamorphic Belt (OMB). Groundwater samples were taken using a packer system from Boeun Hoenam-myun site and Geumsan Suyoung-ri site where several boreholes were dilled with various depths. The geochemical properties and parameters such as temperature, pH, Eh, EC, and DO were directly measured in the site using an in-line measurement method. The concentrations of major cations and anions in the groundwater samples were measured by using ICP-OES (Inductively Coupled Plasma-Optical Emission Spectrometry) and IC (Ion Chromatography), respectively. The concentrations of trace elements including U and Th were measured by using ICP-MS (Inductively Coupled Plasma-Mass Spectrometry) The concentrations of U in the groundwater samples are very low for the Hoenammyun site (0.03~0.69 ppb) and Suyoung-ro site (0.39~1.74 ppb) even though the two sites are uranium deposits and redox conditions are weakly oxidizing. The speciation, saturation index (SI), pH-Eh (Poubaix) diagram were calculated using the Geochemist’s Workbench (GWB 9.0) program and the recent OECD/NEA thermochemical database for U. Calculation results for U speciation in the groundwater samples show that major dissolved uranium species in the groundwater samples are mainly as calcium uranyl carbonate complexes such as Ca2UO2(CO3)3(aq) and CaUO2(CO3)3 2- for almost all groundwater samples. The calculated results for SI and Poubaix diagram also show that the dominant uranium solid phase is a uranyl silicate mineral, uranophane (Ca(H2O)(UVIO2)2 (SiO2)2(OH)6), not uraninite (UIVO2). Since the determination of Eh values for natural groundwater samples is very difficult and uncertain work, we analyzed and discussed the effect of Eh on the geochemical behaviors of U in the groundwater. However, these calculation results are not consistent with the observation for U minerals in rock samples using electron microscopic techniques. Thus, we need further studies to explain the discrepancy between calculation and observation results.

Raman characteristics of various minerals constituting natural rocks collected from uranium deposits in Okcheon metamorphic zone in Korea are presented. Micro-Raman spectra were measured using a confocal Raman microscope (Renishaw in Via Basis). The focal length of the spectrometer was 250 mm, and a 1800 lines/mm grating was installed. The outlet of the spectrometer was equipped with a CCD (1,024256 pixel) operating at -70°C. Three objective lenses were installed, and each magnification was 10, 50, and 100 times. The diameter of the laser beam passing through the objective lens and incident on the sample surface was approximately 2 m. The laser beam power at 532 nm was 1.6 mW on the sample surface. Raman signal scattered backward from the sample surface was transmitted to the spectrometer through the same objective lens. To accurately determine the Raman peak position of the sample, a Raman peak at 520.5 cm-1 measured on a silicon wafer was used as a reference position. Since quartz, calcite, and muscovite minerals are widely distributed throughout the rock, it is easy to observe with an optical microscope, so there is no difficulty in measuring the Raman spectrum. However, it is difficult to identify the uraninite scattered in micrometer sizes only with a Raman microscope. In this case, the location of uraninite was first confirmed using SEM-EDS, and then the sample was transferred to the Raman microscope to measure the Raman spectrum. In particular, a qualitative analysis of the oxidation and lattice conditions of natural uraninite was attempted by comparing the Raman properties of a micrometer-sized natural uraninite and a laboratory-synthesized UO2 pellet. Significantly different T2g/2LO Raman intensity ratio was observed in the two samples, which indicates that there are defects in the lattice structure of natural uraninite. In addition, no uranyl mineral phases were observed due to the deterioration of natural uraninite. This result suggests that the uranium deposit is maintained in a reduced state. Rutile is also scattered in micrometer-sizes, similar to uraninite. The Raman spectrum of rutile is similar in shape to that of uraninite, making them confused. The Raman spectral differences between these two minerals were compared in detail.

Uranium (U) is a hazardous material that can lead to both chemical and radiological toxicity, including kidney damage and health issues associated with radiation exposure. In South Korea. In Korea, where shallow weathered granitic aquifers are widespread, several previous studies have reported high levels of radioactivity in shallow groundwater. This ultimately led to the closure of 60 out of 4,140 groundwater production wells in South Korea. In this study, we examined aquifers currently dedicated to drinking water supply and investigated a dataset of 11,225 records encompassing 103 environmental parameters, based on the random forest classifier. This dataset comprises 80 physical parameters associated with the hydraulic system and 23 chemical parameters linked to water-rock interactions. Among the hydraulic parameters, the presence of a coarse loamy texture in the subsoil displayed a notable positive relationship with the concentration of uranium, implying that it plays a significant role in forming redox conditions for the leaching of uranium from host rocks. Fluorine (F), a major product of water-rock interaction in granitic aquifers, exhibited a positive correlation with the distribution of uranium concentrations. The positive relationship between F concentration and uranium levels suggests that the dissolved uranium originates from groundwater interacting with granites. In conclusion, our findings indicate that two key factors, namely the infiltration capacity of soil layers and the aqueous speciation in groundwater resulting from interactions with local solids, play important roles in determining uranium concentrations in granitic aquifers.