현재, 교통안전진단의 경우 차량 및 보행자의 교통사고를 미연에 방지하고 도로의 전체적인 안전을 도모하고자, 교통안전법 제34조 에 의거하여, 수행 조건에 부합한 경우 교통안전진단을 받도록 규정하고 있다. 교통안전진단의 경우 도로의 구분에 따라 다른 기준을 적용하고 있으며, 도로별 길이를 기준으로 수행 여부를 판단하고 있다. 교통안전진단의 경우 도로의 설계단계, 개시 전 단계 및 운영단계 등 3가지로 구분되어 수행되고 있으며, 각각의 단계별로 진단 수행 내용 및 범위가 조금씩 다르게 진행된다. 설계 단계에서의 교통안전진단의 경우, 해당 도로의 실시 설계 내용을 바탕으로 도로의 안전 을 판단하며, 개시 전 단계의 경우 도로의 신설 이후 운영 전 도로의 안전을 평가한다. 마지막으로 운영 단계의 교통안전진단의 경우 현재 운영 중인 도로에 대하여 도로의 안전을 평가하는 것이다. 본 연구에서는 진단단계별 교통안전진단 중 도로 설계단게에서 수행 시 발생될 수 있는 한계점을 파악하고, 이를 보완할 수 있는 방 안을 제시하여 그 효과를 분석하고자 한다. 또한, 국제 기준으로 운영되고 있는 iRAP(International Road Assessment Programme)의 SR4D( Star Rating for Design)을 통해 설계단계의 교통안전진단 수행 시 효과적이고 안전한 진단결과를 도출해내고자 한다.

An in-wheel motor is a system in which a drive motor is mounted inside a wheel along with a braking device, and the motor inside the wheel directly drives the wheel. An SR motor drive in replace of the conventional PM motor drive for in-wheel motor system has been proposed and analyzed. Two different types of converters were selected and their feasibility in terms of different current control schemes was analyzed and validated through dynamic simulation using PSIM software.

Thermodynamic sorption modeling can enhance confidence in assessing and demonstrating the radionuclide sorption phenomena onto various mineral adsorbents. In this work, Ca-montmorillonite was successfully purified from Bentonil-WRK bentonite by performing the sequential physical and chemical treatments, and its geochemical properties were characterized using X-ray diffraction, Brunauer-Emmett-Teller analysis, cesium-saturation method, and controlled continuous acidbase titration. Further, batch experiments were conducted to evaluate the adsorption properties of Cs(I) and Sr(II) onto the homoionic Ca-montmorillonite under ambient conditions, and the diffuse double layer model-based inverse analysis of sorption data was performed to establish the relevant surface reaction models and obtain corresponding thermodynamic constants. Two types of surface reactions were identified as responsible for the sorption of Cs(I) and Sr(II) onto Ca-montmorillonite: cation exchange at interlayer site and complexation with edge silanol functionality. The thermodynamic sorption modeling provides acceptable representations of the experimental data, and the species distributions calculated using the resulting reaction constants accounts for the predominance of cation exchange mechanism of Cs(I) and Sr(II) under the ambient aqueous conditions. The surface complexation of cationic fission products with silanol group slightly facilitates their sorption at pH > 8.

The effects of La3+ substitution for Sr2+-site on the crystal structure and the dielectric properties of (Ba0.7Sr0.3-3x/2Lax) (Ti0.9Zr0.1)O3 (BSLTZ) (0.005 ≤ x ≤ 0.02) ceramics were investigated. The structural characteristics of the BSLTZ ceramics were quantitatively evaluated using the Rietveld refinement method from X-ray diffraction (XRD) data. For the specimens sintered at 1,550 °C for 6 h, a single phase with a perovskite structure and homogeneous microstructure were observed for the entire range of compositions. With increasing La3+ substitution (x), the unit cell volume decreased because the ionic size of La3+ (1.36 Å) ions is smaller than that of Sr2+ (1.44 Å) ions. With increasing La3+ substitution (x), the tetragonal phase fraction increased due to the A-site cation size mismatch effect. Dielectric constant (εr) increased with the La3+ substitution (x) due to the increase in tetragonality (c/a) and the average B-site bond valence of the ABO3 perovskite. The BSLTZ ceramics showed a higher dielectric loss due to the smaller grain size than that of (Ba0.7Sr0.3)(Ti0.9Zr0.1)O3 ceramics. BSLTZ (x = 0.02) ceramics met the X7R specification proposed by the Electronic Industries Association (EIA).

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).

During the initial cooling period of spent nuclear fuel, Cs-137 and Sr-90 constitute a large portion of the total decay heat. Therefore, separating cesium and strontium from spent nuclear fuel can significantly decrease decay heat and facilitate disposition. This study presents analytical technique based on the gas pressurized extraction chromatography (GPEC) system with cation exchange resin for the separation of Sr, Cs, and Ba. GPEC is a micro-scaled column chromatography system that allows for faster separation and reduction volume of elution solvent compared to conventional column chromatography by utilizing pressurized nitrogen gas. Here, we demonstrate the comparative study of the conventional column chromatography and the GPEC method. Cation exchange resin AG 50W-X12 (200~400 mesh size) was used. The sample was prepared at a 0.8 M hydrochloric acid solution and gradient elution was applied. In this case, we used the natural isotopes 88Sr, 133Cs, and 138Ba instead of radioactive isotopes for the preliminary test. Usually, cesium is difficult to measure with ICP-OES, because its wavelengths (455.531 nm and 459.320 nm) are less sensitive. So, we used ICP-MS to determine the identification and the recovery of eluate. In this study, optimized experimental conditions and analytical result including reproducibility of the recovery, total analysis time and volume of eluents will be discussed by comparing GPEC and conventional column chromatography.

After the Fukushima accident in 2011, relevant concerns regarding the contamination of the natural environment rose abruptly. For example, water contaminated by radionuclides such as Cs and Sr may directly flow into the ocean and threaten the marine ecosystem. In this respect, costeffective and efficient decontamination techniques need to be developed and verified to remediate the contaminated water. Prussian blue (PB) is known as a representative material that can adsorb Cs by ion-trapping and is widely used for medical purposes. However, there is a limitation that PB itself is non-separable and highly mobile in aqueous system, so it needs a fixture, such as bentonite, to be collected after the adsorption. Furthermore, while the performance of PB toward Cs is relatively well known, its behavior toward Sr has rarely been reported. The object of this study is to investigate the sorption characteristics of Cs and Sr onto PB-functionalized bentonite at various conditions. The adsorbent employed in the present work was prepared by mixing bentonite, FeCl3, and K4[Fe(CN)6] at room temperature for 24 hours in the aqueous solution. The concentrations of FeCl3 and K4[Fe(CN)6] were set to a range of 5-200 % compared to the cation exchange capacity of bentonite. After that, the PB-functionalized bentonite was sieved with a mesh size of 63 μm and then reacted with the Cs and Sr solution at various liquid-to-solid (L/S) ratios of 2-10 g/L for up to 500 minutes. Moreover, synthetic seawater containing additional Cs and Sr was reacted with PBfunctionalized bentonite to characterize the ion selectivity of PB. After the completion of the adsorption experiment, a part of the adsorbent was separated and desorption of Cs and Sr with 2 M of nitric acid was performed. For the quantification of aqueous Cs and Sr concentrations, ICP-MS was employed after the filtration with a pore size of 0.45 μm. The result obtained in this study revealed a high sorption affinity of Cs and Sr onto PBfunctionalized bentonite. The analysis results also presented that the sorption reactions of Cs and Sr reached their steady state within 10 minutes of reaction time. Furthermore, the ion selectivity toward Cs and Sr was verified through sorption test with synthetic seawater. According to the high sorption affinity and selectivity, the PB-functionalized bentonite synthesized through this study is expected to be widely used for remediating the Cs- and Sr-contaminated groundwater and seawater, particularly in nuclear waste-relevant industries.

This study investigated the growth behavior and characteristics of compounds formed at the interface between a liquid Al-Si-Cu alloy and solid cast iron. Through microstructural analyses, it was observed that various AlFe and AlFeSi phases are formed at the interface, and the relative proportion of each phase changes when small amounts of strontium are added to the Al alloy. The results of the microstructural analysis indicate that the primary phases of the interfacial compounds in the Al-Si-Cu base alloy are Al8Fe2Si and Al4.5FeSi. However, in the Sr-added alloys, significant amounts of binary AlFe intermetallic compounds such as Al5Fe2 and Al13Fe4 formed, in addition to the AlFeSi phases. The inclusion of Sr has a slight diminishing effect on the rate at which the interfacial compounds layer thickens during the time the liquid Al alloy is in contact with the cast iron. The study also discusses the nano-indentation hardness and micro-hardness of the interfacial phases.

Noise is a sound that people don't want. In this study, noise is measured for SR20, a general aviation trainer used in Korea. In addition, noise measurement points are selected at Muan Airport, where most of the domestic trainers fly under the supervision of the Ministry of Land, Infrastructure and Transport, and the measured data are analyzed based on this. We also want to analyze the noise characteristics of SR20 aircraft through frequency analysis of the noise characteristics of SR20 aircraft are unique. We want to use this to understand what type of noise the trainer affects in future studies. this study will improve the reliability of the noise prediction scenario by comparing and analyzing the actual measured and predicted values when using the noise prediction program.

Several tests should be performed to estimate the structural and chemical stability of the radioactive waste. Among the tests in Gyeongju LILW repository, the leaching test which follows ANS 16.1 standard test method should be conducted for Cs, Sr, and Co radionuclides and must satisfy leachability index larger than 6 which applies deionized water as a leachant. However, the expected leachant inside the silo is groundwater that contains various ions and a high pH condition is predicted due to the concrete structures inside the silo. According to the chemical environment of the leachant, the chemical form of the radionuclides varies from precipitate to ion. Cobalt precipitates when the leachant has high pH environment which is similar condition to the cement-saturated leachant. Unlike the cobalt, cesium is preferred to exist as ion in the high pH condition. Therefore, the significant effect of the chemical environment of the leachant on the leachability of the radionuclides should be considered for the waste acceptance criteria of the radioactive waste repository. From the ‘NRC, Technical position on the waste form, rev1’, the leaching test method should follow the ANS 16.1 methods by using deionized water as leachant, however, a new leachant showing more aggressive leachability can be applied instead of deionized water. In the other hand, ASTM C1308 leaching test method recommends applying actual groundwater of the repository as a leachant. FT-04-020, the leaching test method of France, suggests the ion composition of the groundwater including the pH value. Therefore, the adequacy of using deionized water as leachant for the leaching test method of Cs, Sr, and Co should be re-examined. In this study, the leaching behavior of Cs, Sr, and Co under the several leachant types is estimated. The cement solidified specimen containing single Cs, Sr, and Co were manufactured. The leaching test following ANS 16.1 was performed by applying deionized water, simulated groundater, and cement-saturated groundwater. As a result, a leachability index difference according to the leachant type was discussed. The result of this study is expected to be a background data that helps understanding the actual leaching behavior of the Cs, Sr, and Co in the Gyeongju LILW repository.

According to the Nuclear Safety and Security Commission (NSSC) Notice No. 2021-26 “Delivery Regulations for the Low- and Intermediate Level Radioactive Waste (LILW)”, the activity of 3H, 14C, 55Fe, 58Co, 60Co, 59Ni, 63Ni, 90Sr, 94Nb, 99Tc, 129I, 137Cs, 144Ce, and gross alpha must be identified. Currently, the scaling factor of the dry active waste (DAW) for LILW is applied as an indirect evaluation method in Korea. The analyses are used the destructive methods and 55Fe, 60Co, 59Ni, 63Ni, 90Sr, 94Nb, 99Tc, and 137Cs, which are classified as nonvolatile nuclides, are separated through sequential separation and then measured by gamma detector, liquid scintillation counter (LSC), alpha/beta total counter (Gas Proportional Counter, GPC), and ICP-MS. We will introduce how to apply the existing nuclide separation method and improve the measurement method to supplement it.

The radioactive Sr-90, which is formed from beta decay, is well known as one of the most commonly detected nuclides in radioactive waste. In 2015, it was reported that Sr-90 was observed in some soil and metal wastes among the 516 drums of radioactive waste transferred from the decommissioning site of the Korea Research Reactor (in Seoul) to the disposal site (in Gyeongju). Decontamination and sequestration of radionuclides, including Sr, from nuclear waste is important because they are hazardous and harmful to the ecological environment. Immobilization of these nuclides using a zeolite framework is suitable and simple method that has been widely studied. Therefore, it is still necessary to continuously explore the thermal stability of various zeolites and environmental changes around adsorbed cations in zeolite pore for effective immobilization of these radionuclides. In this study, we observed the thermal stability in fully Sr-exchanged natrolite (Sr-NAT), one of small-pore zeolite, from room temperature to 350°C using the in-situ synchrotron X-ray powder diffraction and thermogravimetric (TGA) analysis. In addition, we investigated the structural changes in Sr-NAT during temperature increase by Rietveld analysis. Sr-NAT exhibited apparent zero thermal expansions (ZTE) with the thermal expansion coefficients of -3(1) × 10-6 at the initial stage of increasing the temperature due to dehydration process. In the section from 250°C to 300°C, a phenomenon like negative thermal expansion (NTE) occurs in which the unit cell volume of Sr-NAT decreases despite the increase in temperature. Sr-NAT maintained well its crystallinity up to 350°C, and it became amorphous at 350°C. In this study, we provide a fundamental understanding of the structural changes and thermal stability mechanism of Sr-exchaged zeolite natrolite with increasing temperature.

Korea faces decommissioning the nation’s first commercial nuclear power plant, the Kori-1 and Wolseong-1 reactors. In addition, other nuclear power plants that will continue to operate will also face decommissioning over time, so it is essential to develop independent nuclear facility decommissioning and site remediation technologies. Among these various technologies, soil decontamination is an essential not only in the site remediation after the decommissioning of the highly radioactive nuclear facility, but also in the case of site contamination caused by an accident during operation of the nuclear facility. But the soil, which is a porous material, is difficult to decontaminate because radionuclides are adsorbed into the pores. Therefore, with the current decontamination technology, it is difficult to achieve the two goals of high decontamination efficiency and secondary waste reduction at the same time. In this study, a soil decontamination process with supercritical carbon dioxide as the main solvent was presented, which has better permeability than other solvents and is easy to maintain critical conditions and change physical properties. Through prior research, a polar chelating ligand was introduced as an additive for smooth extraction reaction between radionuclides present as ions in soil and nonpolar supercritical carbon dioxide. In addition, for the purpose of continuity of the process, a candidate group of auxiliary solvents capable of liquefying the ligand was selected. In this research evaluated the decontamination efficiency by adding the selected auxiliary solvent candidates to the supercritical carbon dioxide decontamination process, and ethanol with the best characteristics was selected as the final auxiliary solvent. In addition, based on the decontamination effect under a single condition of the auxiliary solvent found in the Blank Test process, the possibility of a pre-treatment leaching process using alcohol was tested in addition to the decontamination process using supercritical carbon dioxide. Finally, in addition to the existing Cs and Sr, the possibility of decontamination process was tested by adding U nuclides as a source of contamination. As a result of this research, it is expected that by minimizing secondary waste after the process, waste treatment cost could be reduced and the environmental aspect could be contributed, and a virtuous cycle structure could be established through reuse of the separated carbon dioxide solvent. In addition, adding its own extraction capacity of ethanol used for liquefaction of solid-phase ligands is expected to maximize decontamination efficiency in the process of increasing the size of the process in the future.

Concrete is used as the main engineering barrier in low and intermediate level radioactive waste disposal facilities. As the time passed, the radionuclides stored in repository may contact with groundwater and leak into the ecosystem through the rock media. In this process, the radionuclides can react with calcite via sorption or coprecipitation, because calcite is the major mineral of concrete. Under the various background conditions in repository, frequent dissolution-precipitation reactions can happen. Dissolution of Sr-coprecipitated calcite may be different from that of SrCO3(s) which can mislead the safety performance of radioactive Sr and the estimate of Sr mobility based on the solubility of SrCO3(s). Strontium is not only one of the fission products but also emits beta rays with a long half-life almost 29 years. The strontium may be released or retarded by the dissolution-precipitation reactions in repository. In this study, the dissolution of Sr-coprecipitated with respect to calcite was tested in various environment conditions. The Sr-coprecipitated calcite, (Sr,Ca)CO3(s) was synthesized by coprecipitation method in alkaline condition. The 250 mL of 0.1 M of CaCl2 solution was mixed with 250 mL of 1.14 mM SrCl2·6H2O solution. Then, independently prepared 500 mL of 0.1 M Na2CO3 solution was mixed with the mixed solution of CaCl2 and SrCl2. The precipitates could be made and they were aged for 3 days at room temperature. Then, the supernatant was separated by the centrifugation and the solid at the bottom was dried in an oven at temperature 80°C. After that, the Srcoprecipitated calcite powder was washed using the DI water several times and dried again before use. Characterization of solid powder was conducted by XRD and SEM, and the ICP-MS and ICP-AES were used to analyze the concentrations of Ca and Sr. The batch dissolution experiment was conducted with a solid-to-solution ratio of 10 g/L groundwater in polyethylene tubes. The oxidative groundwater was synthesized by simulating the chemical composition of KAERI Underground Research Tunnel (KURT) DB-3 groundwater. Different temperatures and pHs were prepared and tested for the release of Sr and Ca from the coprecipitated (Sr,Ca)CO3(s) to compare the results with the release of Sr and Ca from SrCO3(s) and CaCO3(s), respectively. Such as, these results will be used to provide better understanding of Sr release and mobility in various repository environments.

Engineered barriers (concrete and grout) in Low- and Intermediate-Level Waste (L/ILW) disposal facilities tend to degrade by groundwater or rainfall water over a long period of time. During the degradation process, radionuclides stored in the disposal facility might be released into the pore water, which can pass through the natural rock barriers (granite and sedimentary rock) and may reach the near-field and far-field. In this transportation, radionuclide might be sorbed onto the engineered and natural rock barriers. In addition, the organic complexing agent such as ethylenediaminetetraacetic acid (EDTA) and α-isosaccharinic acid (ISA), is also present in pore water, which may affect the sorption and mobility of radionuclide. In this study, the sorption and mobility of 90Sr under different conditions such as two pHs (7 and 13), different initial concentrations of organic complexing agents (from 10-5 M to 10-2 M), and solutions (groundwater, pore water, and rainfall water) were investigated in a batch system. The groundwater was collected at the L/ILW disposal facility located at Gyeongju in South Korea. The pore water and rainfall water were artificially made in the laboratory. The concrete, grout, granite, and sedimentary rock samples were collected from the same study sites from where the groundwater was collected. The rock samples were crushed to 53-150 micrometers and were characterized by XRD, XRF, SEM-EDS, BET, and zeta potential analyzer. 90Sr concentration was determined using liquid scintillation counting. The sorption of 90Sr was described by distribution coefficients (Kd) and sorption reduction factor (SRF). In the case of EDTA, the Kd values of 90Sr remained constant from 10-5 M to 10-3 M and tended to decrease at 10-2 M, while in case of ISA the Kd values decreased steadily as the concentration of ISA was increased from 10-5 M to 10-3 M; However, a sudden reduction in the Kd values were observed above 10-2 M. In comparison to EDTA, ISA gave a higher SRF of 90Sr. Therefore, from the above results, it can be concluded that the presence of ISA has a greater effect on the sorption and mobility of radionuclide in the solutions than EDTA, and the radionuclide may reach near- and far-field of the L/ILW disposal facility.

During electrorefining, fission products, such as Sr and Cs, accumulate in a eutectic LiCl-KCl molten salt and degrade the efficiency of the separation process by generating high heat and decreasing uranium capture. Thus, the removal of the fission products from the molten salt bath is essential for reusing the bath, thereby reducing the additional nuclear waste. While many studies focus on techniques for selective separation of fission products, there are few studies on processing monitoring of those techniques. In-situ monitoring can be used to evaluate separation techniques and determine the integrity of the bath. In this study, laser-induced breakdown spectroscopy (LIBS) was selected as the monitoring technique to measure concentrations of Sr and Cs in 550°C LiCl-KCl molten salt. A laser spectroscopic setup for analyzing high-temperature molten salts in an inert atmosphere was established by coupling an optical path with a glove box. An air blower was installed between the sample and lenses to avoid liquid splashes on surrounding optical products caused by laser-liquid interaction. Before LIBS measurements, experimental parameters such as laser pulse energy, delay time, and gate width were optimized for each element to get the highest signal-to-noise ratio of characteristic elemental peaks. LIBS spectra were recorded with the optimized conditions from LiCl-KCl samples, including individual elements in a wide concentration range. Then, the limit of detections (LODs) for Sr and Cs were calculated using calibration curves, which have high linearity with low errors. In addition to the univariate analysis, partial least-squares regression (PLSR) was employed on the data plots to obtain calibration models for better quantitative analysis. The developed models show high performances with the regression coefficient R2 close to one and root-mean-square error close to zero. After the individual element analysis, the same process was performed on samples where Sr and Cs were dissolved in molten salt simultaneously. The results also show low-ppm LODs and an excellent fitted regression model. This study illustrates the feasibility of applying LIBS to process monitoring in pyroprocessing to minimize nuclear waste. Furthermore, this high-sensitive spectroscopic system is expected to be used for coolant monitoring in advanced reactors such as molten salt reactors.

Separation of high heat generating-radioactive isotopes from spent nuclear fuel is an important issue because it can reduce the final disposal area. As one of the technologies that can selectively separate only high heat generating-radioactive isotopes without dissolving spent fuel, the methods using molten salt have recently attracted attention. Although studies on chemical changes of Sr oxides in molten salts have been reported, they have limitation in that alternative oxide reagents rather than oxide fuel were used. In this study, the separation behaviors of Sr from simulated oxide fuel using various molten salts were investigated. A powder type containing 95.7wt% of U and 0.123wt% of Sr was used as the simulated oxide fuel. LiCl, LiCl-CaCl2, MgCl2, LiCl-KCl-MgCl2 and NaCl-MgCl2 were used as molten chloride salts. The separation of Sr from the simulated oxide fuel was conducted by loading it in porous alumina basket and immersing it in a salt. The concentration of Sr in the salt was measured by ICP analysis after sampling the salt outside the basket using dip-stick technique. The separation efficiencies of Sr from simulated oxide fuel using the salts were compared. Furthermore, the causes of their separation efficiency were systematically investigated.