This study aimed to determine the optimal method by analyzing how different fining agents affect the quality of Muscat of Alexandria (MoA) wine. In the initial investigation, MoA wine underwent treatment with bentonite, egg white, icing glass, polyvinylpolypyrrolidone (PVPP), silica, and gelatin. General quality characteristics (pH, total acidity, sugar content, specific gravity, alcohol, volatile acidity), functional components (total polyphenols, antioxidant activity, tannins), and L*, a*, b* values were analyzed. Following the analysis, bentonite demonstrated the best color improvement, while silica and gelatin exhibited high total acidity and effective color enhancement. Consequently, bentonite, gelatin, and silica were deemed suitable for MoA wine and were selected for further investigation. In the second clarification test, varied experiments were conducted on bentonite, silica, and gelatin selected in the first clarification test. Analysis of general quality characteristics and functionality by fining type and time after treatment for MoA wine showed no significant changes before and after treatment. However, an analysis of turbidity after 8 months for each fining agent revealed a superior turbidity improvement effect of 0.040 ± 0.001 in the bentonite treatment group. Additionally, the L value was favorable in the bentonite and silica treatments. Regarding the improvement effect of the b value, silica treatment demonstrated the best results, followed by gelatin treatment.

This study investigated quality characteristics and functionality of rose sparkling wine that were manufactured by secondary fermentation after inoculation of yeast strains. The pH of the samples ranged from 3.96 to 4.05 and total acidity ranged from 0.23 to 0.32%. The alcohol contents of wines ranged from 6.4 to 6.6% and the CO2 pressure ranged from 2.0 to 2.6 bar. The brightness of rose wines ranged from 84.72 to 87.36, the redness from 9.28 to 14.15, and the yellowness from 9.50 to 19.20. The hue value of wines ranged from 1.137 to 1.513 and color intensity ranged from 0.724 to 0.882. Aroma analysis identified 14 alcohols, 22 esters, 4 ketones, 4 acids, and 17 miscellaneous compounds. The total tannin contents and total polyphenol contents of wines were 11.28~12.43 mg% and 24.79~28.20 mg%, respectively. The DPPH radical scavenging activity of wines ranged 63.33 to 67.89% and the ABTS radical scavenging activity of wines 82.16~86.06%. The results of this study provide a basis for establishing the brewing process of rose sparkling wines yeast strains.

The HADES (High-level rAdiowaste Disposal Evaluation Simulator) was developed by the Nuclear Fuel Cycle & Nonproliferation (NFC) laboratory at Seoul National University (SNU), based on the MOOSE Framework developed by the Idaho National Laboratory (INL). As an application of the MOOSE Framework, the HADES incorporates not only basic MOOSE functions, such as multi-physics analysis using Finite Element Method (FEM) and various solvers, but also additional functions for estimating the performance assessment of Deep Geological Repositories (DGR). However, since the MOOSE Framework does not have complex mesh generation and data analyzing capabilities, the HADES has been developed to incorporate these missing functions. In this study, although the Gmsh, finite element mesh generation software, and Paraview, finite element analysis software, were used, other applications can be utilized as well. The objectives of HADES are as follows: (i) assessment of the performance of a Spent Nuclear Fuel (SNF) disposal system concerning Thermal-Hydraulic-Mechanical-Chemical (THMC) aspects; (ii) Evaluation of the integrity of the Engineered Barrier System (EBS) of both general and high-efficiency design perspective; (iii) Collaboration with other researchers to evaluate the disposal system using an open-source approach. To achieve these objectives, performance assessments of the various disposal systems and BMTs (BenchMark Test), conducted as part of the DECOVALEX projects, were studied regarding TH behavior. Additionally, integrity assessments of various DGR systems based on thermal criteria were carried out. According to the results, HADES showed very reasonable results, such as evolutions and distributions of temperature and degree of saturation, when compared to validated code such as TOUGH-FLAC, ROCMAS, and OGS (OpenGeoSys). The calculated data are within the range of estimated results from existed code. Furthermore, the first version of the code, which can estimate the TH behavior, has been prepared to share the contents using Git software, a free and open-source distribution system.

Corrosion-related challenges remain a significant research topic in developing next-generation Molten Salt Reactors (MSRs). To gain a deeper understanding of preventing corrosion in MSRs, previous studies have attempted to improve the corrosion resistance of structural alloys by coating surfaces such as alumina coating. To conduct a corrosion test of coating alloys fully immersed in molten salt, it’s important to ensure that the coating application process is carefully carried out. Ideally, coating all sides of the alloy is necessary to avoid gaps like corners of the alloy, while only applying a one-sided coating alloy can lead to galvanic corrosion with the base metals. Using the droplet shape of eutectic salt applied to only one side of the coating alloy would avoid these problems in conventional corrosion immersion tests, as corrosion would occur solely on the coating surface. Although the droplet method for corrosion tests cannot fully replicate corrosion in the MSRs environment, it offers a valuable tool for comparing and evaluating the corrosion resistance of different coating surfaces of alloys. However, the surface area is important due to the effect of diffusion in the corrosion of alloy in molten salt environments, but it is difficult to unify in the case of droplet tests. Therefore, understanding the droplet-alloy properties and corrosion mechanism is needed to accurately predict and analyze these test systems’ behavior highlighting unity for corrosion tests of different coating surfaces of alloys. To analyze the molten salt droplet behavior on various samples, pelletized eutectic NaCl-MgCl2 was prepared as salt and W-, Mo-coating, and base SS316 as samples. At room temperature, the same mass of pelletized eutectic NaCl-MgCl2 was placed on different samples under an argon atmosphere and heated to a eutectic point of 500°C in a furnace. After every hour, the molten droplets were hardened by rapid cooling at room temperature outside the furnace. The mass loss of salts and the contact area of the samples were measured by mass balance and SEM. The shape, surface area to volume ratio, and evaporation of the droplets of NaCl-MgCl2 per each coating sample and hour were analyzed to identify the optimal mass to equalize the contact coating surface of alloys with salts. Furthermore, We also analyzed whether their results reached saturation of corrosion products through ICP-MS. This will be significant research for the uniformity of the liquid-drop shape corrosion test of the coating sample in molten eutectic salts.

LiCl-KCl eutectic possesses unique properties such as a low melting point, high thermal conductivity, and good electrical conductivity. These properties make it suitable for various applications, including nuclear power generation, pyroprocessing in nuclear waste management, and thermal energy storage systems. In most experiments using LiCl-KCl, the molten salt composition is an important factor; therefore, periodic analysis through sampling is necessary for monitoring compositional changes. Although manual sampling is typically used, it is time-consuming and can introduce errors due to low reproducibility. To address this issue, we have developed an automatic molten salt sampling device using the cold-finger method. This method involves immersing the tip of a tungsten rod in hightemperature LiCl-KCl, removing it after a few seconds, and allowing the adhered molten salt to solidify instantly. A collector then scratches and drops the solidified sample. These processes are carried out automatically using servo motors, enabling the sampling device to move around the molten salt system. We have optimized the sampling conditions, such as insertion and withdrawal rate, immersion time, and the interval between continuous sampling, based on the molten salt temperature. The temperature was set between 500°C and 850°C, considering the operating temperatures of the applications. In addition to sampling speed, the sampling depth is a key condition for determining the sampling mass. Therefore, we examined the amount of sample depending on the sampling depth and, particularly, considered the change in salt height when sampling is performed continuously. As a result, we determined the number of sampling iterations required to reach the target sample mass. Furthermore, to minimize the initial salt loss, we noted that sampling from the salt surface resulted in less representative samples. To determine the reliability, we compared the results of surface sampling with those obtained when sampling at the middle of the salt. This study will enable highly reproducible and reliable sampling by providing a prototype for an automatic sampling device for molten salt along with guidelines.

Measuring the concentration of corrosion products or nuclear fission products (FPs) in molten salts is crucial for pyroprocessing and molten salt reactors. Electrochemical analysis methods that can be performed in situ offer significant advantages for monitoring the concentration of corrosion products or FPs in molten salts. A microelectrode is an electrode with a length of several tens of micrometers on one side. The use of a microelectrode for electrochemical analysis has several advantages due to its small size, including rapidly reaching the limiting current regardless of the scan rate, immediate attainment of the limiting current upon applying an overpotential for instant monitoring within milliseconds, accurate measurement even in low convection systems, a small iR drop resulting from low flowing current and high signal accuracy, and high current density resulting in a high signal-tonoise ratio (SNR). Among various methods for making microelectrodes, techniques involving cutting a thin wire or using capillaries (such as the dual-bore capillary and pulled glass capillary methods) require precise manual skills and experience. Therefore, the results may vary depending on the maker’s skill level, and it can be difficult to control the electrode’s area, thickness, and surface uniformly. Recent research has focused on using semiconductor processes to fabricate microelectrodes, where CVD, metal sputtering, photolithography, and etching processes work together to deposit, refine, and shape the required material on a silicon wafer to create microelectrodes. However, the durability of microelectrodes produced this way is still low (usable for about 15-30 minutes), and there is no clear research on the degradation mechanism over time. To verify the proper operation of the fabricated microelectrodes, cyclic voltammetry (CV) is performed at various scan rates (from 10 mVs-1 to 2 Vs-1), and chronoamperometry (CA) is also examined to confirm whether the electrodes rapidly reach a steady-state current. After confirming their proper operation, CV is continuously measured until the microelectrodes are destroyed in a LiCl-KCl solution containing a small amount of FPs (Sm 340 mM) at 450°C. By observing changes in the electrical signal of the microelectrodes over time, the durability is evaluated, and the mechanism of performance degradation of the electrode is discovered. The experiment is then repeated by gradually increasing the temperature by 30°C from 450°C up to 600°C to observe the changes with temperature. This study provides basic information for future microelectrode experiments, and by diagnosing the cause of destruction, a more durable microelectrode structure can be manufactured.

Molten salt reactors have several advantages over conventional light water reactors. These include producing less nuclear waste, operating at higher power efficiency and inherent safety due to the low operating pressure. NaCl-MgCl2 eutectic salt is one of the candidates for the molten salt reactor coolant. However, because the salt is very hygroscopic, structural material corrosion occurs resulting in the high cost to maintain. To mitigate corrosion there have been many studies for the dehydration of the salt, especially focusing on the magnesium chloride. The reason is that the moisture adsorbed to the magnesium chloride undergoes hydrolysis over 200 degrees Celsius and decomposes to MgOHCl while the moisture associated with the NaCl is easily liberated during the heating procedure without chemical reaction. As the operating temperature of the molten salt is between 500 and 700 degrees Celsius, the MgOHCl is believed as the main cause for the structural corrosion. In this research, thermal dehydration of the salt with elemental Mg, for the NaCl-MgCl2 eutectic, was studied based on the previous dehydration methods and considering scalable and easy to handle. The MgOHCl was removed both through the thermal decomposition and the reduction by Mg metal. After the removal of MgOHCl, based on the difference between the freezing points and the density, the salt cooled down very slowly to ensure the separation between the purified salt and the disposals such as MgO and remaining Mg metals. The efficiency of the dehydration method was determined by the concentration of the MgOHCl. The concentration was determined by cyclic voltammetry and the result was compared with undehydrated salt and salt dehydrated thermally without the addition of Mg metal. To qualify and quantify the MgOHCl content through the cyclic voltammetry, it was necessary to observe the signal by adding MgOHCl to each sample. Based on the thermogravimetric analysis result of MgCl2· 6H2O, MgOHCl powder was formed through heating the MgCl2·6H2O.

Radioactive wastes, including used nuclear fuel and decommissioning wastes, have been treated using molten salts. Electrochemical sensors are one of the options for in-situ process monitoring using molten salts. However, in order to use electrochemical sensors in molten salt, the surface area must be known. This is because the surface area affects the current of the electrode. Previous studies have used a variety of methods to determine the electrode surface area in molten salts. One method of calculating the electrode surface area is to use the reduction current peak difference between electrodes with known length differences. The method is based on the reduction peak and has the benefit of providing long-term in-situ monitoring of surfaces immersed in molten salt. A number of assumptions have been made regarding this method, including that there is no mass transport by migration or convection; the reaction is reversible and limited by diffusion; the chemical activity of the deposit should be unity; and species should follow linear diffusion. For the purpose of overcoming these limitations, a variety of machine learning algorithms were applied to different voltammogram datasets in order to calculate the surface area. Voltammogram datasets were collected from multiarray electrodes, comprising a multiarray holder, two tungsten rods (1 mm diameter) working electrodes, a quasi-reference electrode, and a counter electrode. The multiarray electrode holder was connected to the auto vertical translator, which uses a servo motor, for changing the height of the rod in the molten salts. To make big and diverse data for training machine learning models, various concentrations of corrosion products (Cr, Fe) and fission products (Eu, Sm) in NaCl-MgCl2 eutectic salts were used as electrolyte; electrolyte temperatures were 500, 525, 550, 575, and 600°C. This study will demonstrate the potential of utilizing machine learning based electrochemical in situ monitoring in molten salt processing.

Aluminum’s exceptional properties, such as its high strength-to-weight ratio, excellent thermal conductivity, corrosion resistance, and low neutron absorption cross-section, make it an ideal material for diverse nuclear industry applications, including aluminum plating for the building envelope of nuclear power plants. However, plating aluminum presents challenges due to its high reactivity with oxygen and moisture, thus, complicating the process in the absence of controlled environments. Plating under an inert atmosphere is often used as an alternative. However, maintaining an inert atmosphere can be expensive and presents an economic challenge. To address these challenges, an innovative approach is introduced by using deep eutectic solvents (DES) as a substitute for traditional aqueous electrolytes due to the high solubility of metal salts, and wide electrochemical window. In addition, DESs offer the benefits of low toxicity, low flammability, and environmentally friendly, which makes DESs candidates for industrial-scale applications. In this study, we employed an AlCl3-Urea DES as the electrolyte and investigated its potential for producing aluminum coatings on copper substrates under controlled conditions, for example, current density, deposition duration, and temperature. A decane protective layer, non-polar molecular, has been used to shield the AlCl3-Urea electrolyte from the air during the electrodeposition process. The electrodeposition was successful after being left in the air for two weeks. This study presents a promising and innovative approach to optimizing aluminum electrodeposition using deep eutectic solvents, with potential applications in various areas of the nuclear industry, including fuel cladding, waste encapsulation, and radiation shielding.

Metakaolin-based geopolymers have shown promise as suitable candidates for 14C immobilization and final disposal. It has been shown that the physicochemical properties of metakaolin wasteforms meet, and often far exceeding, the strict compression strength and leaching acceptance criteria of the South Korea radioactive waste disposal site. However, it is not possible to analyze and characterize the internal structure of the geopolymer wasteform by conventional characterization techniques such as microscopy without destruction of the wasteform; an impractical solution for inspecting wasteforms destined for final disposal. Internal inspection is important for ensuring wastes are homogenously mixed throughout the wasteform and that the wasteform itself does not pose any significant defects that may have formed either during formulation and curing or as a result of testing prior to final disposal. X-ray Computed Tomography (XCT) enables Non-Destructive Evaluation (NDE) of objects, such as final wasteforms, allowing for both their internal and external, characterization without destruction. However, for accurate quantification of an objects dimensions the spatial resolution (length and volume measures) must be know to a high degree of precision and accuracy. This often requires extensive knowledge of the equipment being used, its precise set-up, maintenance and calibration, as well as expert operation to yield the best results. A spatial resolution target consists of manufactured defects of uniformed dimensions and geometries which can be measured to a high degree of accuracy. Implementing the use of a spatial resolution target, the dimensions of which are known and certified independently, would allow for rapid dimensional calibration of XCT systems for the purpose of object metrology. However, for a spatial resolution target to be practical it should be made of the same material as the intended specimen, or at least exhibit comparable X-ray attenuation. In this study, attempts have been made to manufacture spatial resolution targets using geopolymer, silica glass, and alumina rods, as well as 3D printed materials with varying degrees of success. The metakaolin was activated by an alkaline activator KOH to from a geopolymer paste that was moulded into a cylinder (Diameter approx. 25 mm). The solidified geopolymer cylinder as well as both the silica glass rod and alumina rod (Diameter approx. 25 mm) we cut to approximately 4 mm ± 0.5 mm height with additional end caps cut measuring 17.5 mm ± 2.5 mm height. All parts were then polished to a high finish and visually inspected for their suitability as spatial resolution targets.