This work provided a review of three techniques—(1) spectrochemical, (2) electrochemical, and (3) spectroelectrochemical– for molten salt medias. A spectroelectrochemical system was designed by utilizing this information. Here, we designed a spectroelectrochemical cell (SEC) and calibrated temperature controllers, and performed initial tests to explore the system’s capability limit. There were several issues and a redesign of the cell was accomplished. The modification of the design allowed us to assemble, align the system with the light sources, and successfully transferred the setup inside a controlled environment. A preliminary run was executed to obtain transmission and absorption background of NaCl-CaCl2 salt at 600°C. It shows that the quartz cuvette has high transmittance effects across all wavelengths and there were lower transmittance effects at the lower wavelength in the molten salt media. Despite a successful initial run, the quartz vessel was mated to the inner cavity of the SEC body. Moreover, there was shearing in the patch cord which resulted in damage to the fiber optic cable, deterioration of the SEC, corrosion in the connection of the cell body, and fiber optic damage. The next generation of the SEC should attach a high temperature fiber optic patch cords without introducing internal mechanical stress to the patch cord body. In addition, MACOR should be used as the cell body materials to prevent corrosion of the surface and avoid the mating issue and a use of an adapter from a manufacturer that combines the free beam to a fiber optic cable should be incorporated in the future design.

Electroanalytical study for the rotating cylinder electrode in molten LiCl-KCl eutectic salt (58– 42mol%) containing MgCl2 (0.1wt%) at 600°C is conducted. The researches of rotating cylinder electrode have been widely conducted for the century. The advantage of the electrode is that it can mitigate the unintended natural convection by providing a controlled diffusion boundary layer thickness. However, the experimental data for the high temperature molten salts is barely existed. The study adopts the electrochemical techniques such as cyclic voltammetry for the static cell and linear sweep voltammetry for the dynamic cell to calculate the diffusion coefficient. The peak current density and limiting current density are measured according to the scan rate. In order to evaluate the mass transfer under hydrodynamic flow condition, the revolution speeds of cylindrical electrode are varied from 10 rpm to 500 rpm which are corresponded to the Reynolds number of 4 and 185 respectively. The flow regime covers from the laminar to semi-turbulent regime (transient) as the critical Reynolds number Recrit is 200. The limiting current density shows a linear trend with the revolution speed and agrees well with the existing mass transfer correlations. For the extended flow regime, a new mass transfer correlation is suggested as the relation of non-dimensional numbers (Sh = aRebScc) based on the dimensionless analysis.

At high temperatures, molten salt has heat transfer properties like water. Molten salt has the characteristics of a strong natural circulation tendency, large heat capacity, and low thermal conductivity. Unlike sodium, molten salt does not react explosively exothermically with air. However, molten salt has a strong tendency to corrode materials, and its properties are easily changed by a sensitive reaction to oxygen and moisture. Therefore, it is necessary to study material corrosion properties and chemical control methods for nuclear fuel salts, which are eutectic mixtures. In this study, the optimal operation method of the thermal convection loop is established to perform the experiments on the molten salt. The process describes briefly as follows. The operation step consists of preparation, purification, transportation, and operation. In the preparation, the step checks the entire structure and equipment (TC, blower, vacuum pump, etc.). And melt the salt mixture at a high temperature (670°C) slowly in the purification step. Before injecting the molten salt, the surface temperature of the entire loop must retain temperature (about 500°C) constantly. Completely melted molten salt in the melting pot is flow along the pipe of the thermal convection loop in the transportation step. Lastly, the convection of molten salt goes to keep by the temperature difference. The thermal convection loop can be utilized for various experiments such as corrosion tests, component analyses, chemistry control, etc.

Molten salt used in the multipurpose molten salt experiment must be of high purity. Depending on the purpose of the experiment, only the base component of the molten salt be used, or a component simulating a nuclear fission product be added to the base component and used. In all cases, an increase in the concentration of impurities such as oxygen and moisture may lead to an erroneous interpretation when analyzing the experimental results. Therefore, molten salt should be purified before use. In this study, the purification of molten salt is described for multi-purpose molten salt experiments. The salt mixture is selected as MgCl2-NaCl and is quantified at a mixing ratio of 43mol%:57mol%. The salt mixture is treated in a glove box environment because of must minimize the reaction of adsorbing oxygen and moisture when the salt mixture is exposed to the atmosphere. MgCl2 is more likely to contain water than NaCl, the purification of the NaCl-MgCl2 mixture is established according to the purification process for removing water from MgCl2. A process for purifying the salt mixture briefly consists as follows: drying moisture, melting salts, purification, removing HCl, and stabilization. Through the process be able to obtain high-purity molten salt and more accurate experiment results.

A molten salt reactor (MSR) has considerably attracted attention due to its several advantages for the safety and efficiency over the light water reactors. Because the structural material in MSR is contacted with high-temperature liquid fuel during long-term, the excellent material for corrosion resistance is required to be applied in MSR. In this study, we evaluated the corrosion resistance for alloy 600 and 617, which are the nickel-based materials, in KCl molten salt at 800ºC for 100 h under Ar atmosphere containing less than 1 ppm of moisture and oxygen. After the corrosion experiments of alloy 600 and 617, the amount of the weight loss for them caused by the KCl molten salt were determined. In addition, the variation in the crystal structure, surface morphology, and elemental distribution was examined using X-ray diffraction and scanning electron microscopy equipped with energy dispersive X-ray spectroscopy.

Molten salt immersion technique has been tested with several Sr oxides, SrZrO3, SrMoO4 and U2SrOy, and MgCl2 based molten salts for the Sr nuclide separation. Reaction time, temperature, and salt composition were varied to effectively separate Sr in chloride forms. ICP-OES, XRD, and SEM analysis were conducted for the conversion efficiency and structure and morphology analysis. It is confirmed that all experiments of SrZrO3 with MgCl2 at 800°C for reaction time 5, 10, 20 hours showed higher conversion efficiency than 99% and in LiCl-KCl-MgCl2 and NaCl-MgCl2 molten salts at 500°C or 600°C, conversion efficiency higher than 97% was obtained. SrMoO4 in MgCl2 immersion experiments for 10 hours showed higher conversion efficiency than 99% when the molar ratio of salt/oxide powder is 7. U2SrOy was also tested with MgCl2 molten salt at 800°C and higher efficiency than 99% and mainly MgUO4 were produced as a reaction product.

To estimate the removal efficiency of TRU and rare earth elements in an oxide spent fuel, basic dissolution experiments were performed for the reaction of rare earth elements from the prepared simfuel with chlorination reagents in LiCl-KCl molten salt. Based on the literature survey, NH4Cl, UCl3, and ZrCl4 were selected as chlorination reagent. CeO2 and Gd2O3 powders were mixed with uranium oxide as a representative material of rare earth elements. Simfuel pellets were prepared through molding and sintering processes, and mechanically pulverized to a powder form. The experiments for the reaction of the simfuel powder and chlorination reagents were carried out in a LiCl-KCl molten salt at 500°C. To observe the dissolution behavior of rare earth elements, molten salt samples were collected before and after the reactions, and concentration analysis was performed using ICP. After the reaction completed, the remaining oxide was washed with water and separated from the molten salt, and XRD was used for structural analysis. As a result of salt concentration analysis, the dissolution performance of rare earth elements was confirmed in the reaction experiments of all chlorination reagents. In an experiment using NH4Cl and ZrCl4, the uranium concentration in the molten salt was also measured. In other words, it seemed that not only rare elements but also uranium oxide, which is a main component of simfuel, was dissolved. Therefore, it is thought that the dissolution of rare earth elements is also possible due to the collapse of the uranium oxide structure of the solid powder and the reaction with the oxide of rare earth elements exposed to molten salt. As a result of analyzing the concentration changes of Simfuel before and after each reaction, there was little loss of uranium and rare earth elements (Ce/Gd) in the NH4Cl experiment, but a significant amount of rare earth elements were found to be reduced in the UCl3 experiment, and a large amount of rare earth elements were reduced in the ZrCl4 reaction.

Strontium-90 is a high heat-generating nuclide in spent nuclear fuel. The removal of the nuclide separation is indispensable to reduce the burden of storage and disposal of high-level radioactive waste. Korea Atomic Energy Research Institute has developed the molten salt immersion technique to separate the strontium by the chlorination of the strontium oxide in molten salt. It is needed to separate the salt for the recovery of strontium from the salt solution after the chlorination reaction. In this study, it was investigated on the recovery of the strontium from the salt. Vacuum distillation was used for the separation of strontium from the molten salt. The vapor pressures of the candidate salts were calculated by HSC chemistry and the apparent evaporation rates (AER) were measured at 830°C to evaluate the salts for strontium recovery. The candidate salts were LiCl, KCl, MgCl2, NaCl and CaCl2. The AERs of MgCl2 and NaCl were 1.9 and 1.3 g/cm2-h, respectively. Those two salts can be separated from the strontium compound even though the AER values are much lower than those of LiCl-KCl (~ 8 g/cm2-h). CaCl2 salt was rarely evaporated (AER < 0.03 g/cm2-h) and it is not suitable to use as a strontium recovery salt. Therefore, MgCl2, NaCl, LiCl and KCl can be regarded as candidates for a strontium recovery salt.

Molten Salt Reactor (MSR) is one of the generation-IV advanced nuclear reactors in which hightemperature molten salt mixture is used as the primary coolant, or even the fuel itself unlike most nuclear reactors that adopt solid fuels. The MSR has received a great attention because of its excellent thermal efficiency, high power density, and structural simplicity. In particular, since the MSR uses molten salts with boiling points higher than the exit temperature of the reactor core, there is no severe accident such as a core melt-down which leads to a hydrogen explosion. In addition, it is possible to remove the residual heat through a completely passive way and when the fuel salt leaks to the outside, it solidifies at room-temperature without releasing radioactive fission products such as cesium, which make the MSR inherently safe. Both fluoride and chloride mixtures can be used as liquid fuel salts by adding actinide halides for MSRs. However, the MSRs using chloride-based salt fuels can be operated for a long time without adding nuclear fuel or online reprocessing because the actinide solubility in chloride salts is about six times higher than that in fluoride salts. Therefore, the chloride-based MSRs are more effective for the transmutation of long-lived radionuclides such as transuranic elements than the fluoride-based MSRs, which is beneficial to resolve the high radioactive spent nuclear fuel generated from light water reactors (LWRs). This paper examines liquid fuel fabrication using an improved U chlorination process for the chloride-based MSRs and presents the strategy for the management of gaseous fission products generated during the operation of MSR.

The aim of this review is to communicate some essential knowledge of the underlying mechanism of the corrosion of structural containment alloys during molten salt reactor operation in the context of prospective online monitoring in future MSR installations. The formation of metal halide species and the progression of their concentration in the molten salt do reflect containment corrosion, tracing the depletion of alloying metals at the alloy salt interface will assure safe conditions during reactor operation. Even though the progress of alloying metal halides concentrations in the molten salt do strongly understate actual corrosion rates, their prospective 1st order kinetics followed by near-linearly increase is attributed to homogeneous matrix corrosion. The service life of the structural containment alloy is derived from homogeneous matrix corrosion and near-surface void formation but less so from intergranular cracking (IGC) and pitting corrosion. Online monitoring of corrosion species is of particular interest for molten chloride systems since besides the expected formation of chromium chloride species CrCl2 and CrCl3, other metal chloride species such as FeCl2, FeCl3, MoCl2, MnCl2 and NiCl2 will form, depending on the selected structural alloy. The metal chloride concentrations should follow, after an incubation period of about 10,000 hours, a linear projection with a positive slope and a steady increase of < 1 ppm per day. During the incubation period, metal concentration show 1st order kinetics and increasing linearly with time1/2. Ideally, a linear increase reflects homogeneous matrix corrosion, while a sharp increase in the metal chloride concentration could set a warning flag for potential material failure within the projected service life, e.g. as result of intergranular cracking or pitting corrosion. Continuous monitoring of metal chloride concentrations can therefore provide direct information about the mechanism of the ongoing corrosion scenario and offer valuable information for a timely warning of prospective material failure.

In this work, the sulfonic acid group was introduced into the resorcinol–formaldehyde (RF) microspheres by the addition of p-phenolsulfonic acid during the polycondensation process of RF. The hydrophilicity of the sulfonated RF allowed KOH to infiltrate inside the microspheres, which enhanced the formation of mesopores in the carbon microspheres during the activation process by KOH. SEM and TEM observations and N2 adsorption measurements verified the formation of abundant mesopores in the porous carbon microspheres. The BET surface area of these mesoporous carbons exceeded 2000 m2/ g. In 17 m NaClO4 “water-in-salt” (WIS) electrolyte-based supercapacitor, the synthesized mesoporous carbon exhibited high specific capacitance of 170 F/g at current density of 0.5 A/g, comparable to those in regular KOH electrolyte. When graphite was used as current collectors, the symmetric cell could operate at 2.5 V, and the mesoporous carbon exhibited an energy density of 43 Wh/kg at power density of 0.25 kW/kg, and 25 Wh/kg at power density of 6.25 kW/kg, respectively, which were superior to those using Pt or stainless steel as current collectors. The mesoporous carbon/graphite was an excellent electrode in new-generation “WIS” electrolyte-based high-voltage supercapacitor due to their high energy and power density.

High-performance carbon materials were prepared via a one-step molten salt carbonization of tobacco waste used as electrode materials for supercapacitors. Carbon material prepared by carbonization for 3 h in molten CaCl2 at 850 °C exhibits hierarchically porous structure and ideal capacitive behavior. In a three-electrode configuration with 1 mol L− 1 H2SO4 aqueous solution, it delivers specific capacitance of 196.5 F g− 1 at 0.2 A g− 1, energy density of 27.2 Wh kg− 1 at 0.2 A g− 1, power density of 983.5 W kg− 1 at 2 A g− 1, and excellent cyclic stability with 94% capacitance retention after 5000 charge–discharge cycles at 1 A g− 1. Moreover, in a symmetrical two-electrode configuration with 6 mol L− 1 KOH aqueous solution, it delivers specific capacitance of 111.1 F g− 1 at 0.2 A g− 1, energy density of 3.8 Wh kg− 1 at 0.2 A g− 1, and power density of 482.0 W kg− 1 at 2 A g− 1. The relationship between hierarchically porous structure and capacitive performance is also discussed.

염장(鹽醬)은 고대부터 현재에 이르기까지 한국의 기저 음식으로 밥, 국, 반찬으로 구성된 한국 식사구조에서 빠질 수 없는 음식물이다. 본고는 삼국 시대에서 조선 시대에 이르는 불교사찰과 일반사회의 식재료로서의 염장의 내용을 개괄하고 고려 시대 원감국사 충지(圓鑑國師 冲止)의 시문을 통해 불교 수행자로서 산중 음식 생활에서의 염장의 모습과 선어(禪語)로서 염장이 선불교의 수행과 깨달음에서 어떠한 상징과 의미로 사용되었는지를 고찰하였다. 이 연구에서 통일신라 시대 불교사원의 장독대인 장고(醬庫), 고려 시대 태안 마도선의 동식물, 음식유물은 해당 시기 음식문화를 밝히는 핵심자료로 기능하였으며 각 시기 문헌 자료와 더불어 상호보완적으로 당시의 음식실태에 객관성을 부여하는 기능을 하였다. 산중사찰 수행자의 염장 생활과 선어(禪語)와 선지(禪旨)로서의 염장고찰은 원감국사의 시문을 통해 평상심시도(平常心是道)와 화두로 정착하는 모습을 고찰하였다.

The growth characterization and enzyme productivity of halotolerant microorganisms isolated from the Nakdong River estuary wetland in Korea were investigated in this study. The isolation of halotolerant microorganisms was carried out through their cultivation at 37oC for several days using a marine agar medium. After a single-colony isolation, 16 pure colonies were obtained, and phylogenetic analysis was done using 16S-based ID service in the EzBioCloud database. The isolated strains were divided into 3 phyla, 5 families, 7 genera, and 13 species. Possible industrial applications of the strains were confirmed upon testing for amylolytic, lipolytic, and proteolytic activity to confirm the possible production of hydrolytic enzymes, growth at a pH range of 5 to 9, and various salt concentrations being tested. Thirteen strains possessed at least one enzyme activity, and 5 strains possessed 2 enzyme activities. Eight strains could tolerate up to 10% NaCl concentration. This result indicated that isolated strains had shown the possible application in food and cosmetic industries. Therefore, this study would contribute to securing domestic biological resources and improving hydrolytic enzyme activity using these strains.