Chelating agents like ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTPA), and nitrilotriacetic acid (NTA) find extensive application in the removal of residual substances due to their high stability constants with a wide range of metal ions. They also play a crucial role in nuclear decontamination operations aimed at eliminating metallic radionuclides such as 60Co, 90Sr, and 239Pu. However, improper disposal of chelated radioactive waste can lead to significant increases in radionuclide migration rates from disposal sites. Therefore, it is imperative to comprehend the behavior of chelating agents under varying conditions, including pH, temperature, and metal ion concentrations. In this study, we present the results of a pH-dependent composition analysis of nickel-chelate complexes using UV-Vis spectrophotometry. Nickel (Ni) serves as an ideal metal ion for investigating its interactions with chelating agents due to its solubility over a wide pH range and high stability constants with all three chelating agents mentioned earlier. Initially, UV-Vis spectra of Ni-EDTA, Ni-DTPA, and Ni-NTA complexes were recorded at various pH levels. We assigned absorption maxima and compared our findings with existing literature on each Ni-chelate complex. Furthermore, we examined mixed samples of all three complexes, varying the pH to monitor changes in composition. The results and their implications will be presented in our poster presentation.

The physicochemical similarities of hydrogen isotopes have made their separation a challenging task. Conventional methods such as cryogenic distillation, Girdler sulfide process, chromatography, and thermal cycling absorption have low separation factors and are energy-intensive. To overcome these limitations, research has focused on kinetic quantum sieving (KQS) and chemical affinity quantum sieving (CAQS) effects for selective separation of hydrogen isotopes. Porous materials such as metal-organic frameworks (MOF), covalent organic frameworks (COF), zeolites, carbon, and organic cages have been studied for hydrogen separation. In this study, we focus the enhancement for CAQS to provide the cations due to the chemical affinity between hydrogen isotope and unsaturated sites by cations in zeolite beads. Cation exchanged zeolite beads was synthesized with cobalt, copper, nickel, iron and silver in zeolite 4A beads. Synthesized cation exchanged zeolite was analyzed for the surface area and pore size in N2 and adsorption behaviors of hydrogen isotopes (D2/H2) for various cation exchanged zeolite beads using BET at 77 K. The study predicts the D2/H2 adsorption selectivity based on the results obtained with BET. These hydrogen isotope adsorption results will provide a foundation for future processes for tritium separation.

The solid-state chemistry of uranium is essential to the nuclear fuel cycle. Uranyl nitrate is a key compound that is produced at various stages of the nuclear fuel cycle, both in front-end and backend cycles. It is typically formed by dissolving spent nuclear fuel in nitric acid or through a wet conversion process for the preparation of UF6. Additionally, uranium oxides are a primary consideration in the nuclear fuel cycle because they are the most commonly used nuclear fuel in commercial nuclear reactors. Therefore, it is crucial to understand the oxidation and thermal behavior of uranium oxides and uranyl nitrates. Under the ‘2023 Nuclear Global Researcher Training Program for the Back-end Nuclear Fuel Cycle,’ supported by KONICOF, several experiments were conducted at IMRAM (Institute of Multidisciplinary Research for Advanced Materials) at Tohoku University. First, the recovery ratio of uranium was analyzed during the synthesis of uranyl nitrate by dissolving the actual radioisotope, U3O8, in a nitric acid solution. Second, thermogravimetric-differential thermal analysis (TG-DTA) of uranyl nitrate (UO2(NO3)2) and hyper-stoichiometric uranium dioxide (UO2+X) was performed. The enthalpy change was discussed to confirm the mechanism of thermal decomposition of uranyl nitrate under heating conditions and to determine the chemical hydrate form of uranyl nitrate. In the case of UO2+X, the value of ‘x’ was determined through the calculation of weight change data, and the initial form was verified using the phase diagram for the U-O system. Finally, the formation of a few UO2+X compounds was observed with heat treatment of uranyl nitrate and uranium dioxide at different temperature intervals (450°C-600°C). As a result of these studies, a deeper understanding of the thermal and chemical behavior of uranium compounds was achieved. This knowledge is vital for improving the efficiency and safety of nuclear fuel cycle processes and contributes to advancements in nuclear science and technology.

Once discharged, spent nuclear fuel undergoes an initial cooling process within deactivation pools situated at the reactor site. This cooling step is crucial for reducing the fuel’s temperature. Once the heat has sufficiently diminished, two viable options emerge: reprocessing or interim storage. A method known as PUREX, for aqueous nuclear reprocessing, involves a chemical procedure aimed at separating uranium and plutonium from the spent nuclear fuel. This separation not only minimizes waste volume but also facilitates the reuse of the extracted materials as fuel for nuclear reactors. The transformation of uranium oxides through dissolution in nitric acid followed by drying results in uranium taking the form of UO2(NO3)2 + 6H2O, which can then be converted into various solid-state configurations through different heat treatments. This study specifically focuses on investigating the phase transitions of artificially synthesized UO2(NO3)2 + 6H2O subjected to heat treatment at various temperatures (450, 500, 550, 600°C) using X-ray Diffraction (XRD) analysis. Heat treatments were also conducted on UO2 to analyze its phase transformations. Additionally, the study utilized XRD analysis on an unidentified oxidized uranium oxide, UO2+X, and employed lattice parameters and Bragg’s law to ascertain the oxidation state of the unknown sample. To synthesize UO2(NO3)2 + 6H2O, U3O8 powder is first dissolved in a 20% HNO3 solution. The solid UO2(NO3)2 + 6H2O is obtained after drying on a hotplate and is subsequently subjected to heat treatment at temperatures of 450, 500, 550, and 600°C. As the heat treatment temperature increases, the color of the samples transitions from orange to dark green, indicating the formation of different phases at different temperatures. XRD analysis confirms that uranyl nitrate, when heattreated at 500 and 550°C, oxidizes to UO3, while the sample subjected to 600°C heat treatment transforms into U3O8 due to the higher temperature. All samples exhibit sharp crystal peaks in their XRD spectra, except for the one heat-treated at 450°C. In the second experiment, the XRD spectra of the heat-treated UO2 consistently indicate the presence of U3O8 rather than UO3, regardless of the temperature. Under an oxidizing atmosphere within a temperature range of 300 to 700°C, UO2 can be oxidized to form U3O8. In the final experiment, the oxidation state of the unknown UO2+X was determined using Bragg’s law and lattice parameters, revealing that it was a material in which UO2 had been oxidized, resulting in an oxidation state of UO2.24.

We investigated the behavioral attractive responses of a lepidopteran larva parasite, Exorista japonica to 10 synthetic herbivore-induced plant volatiles (HIPVs). These synthetic HIPVs have been revealed the attractive effect on several parasites. For each of the HIPVs, we asked the following two questions : (1) Which volatiles show the attractiveness to this parasitoid, (2) Whether the attractant directly or indirectly affects the host settlement and parasitism of the parasitoid. To experimentally address these questions, we performed 2 and 4 choice indoor cage tests. E. japonica adults were significantly attracted to benzaldehyde and (Z)-3-hexen-1-ol showing higher settlement and parasitic rates on Spodoptera litura of treatments. Compared to the untreated plots, the average parasitism of E. japonica on S. litura larvae in the benzaldehyde treatments increased by approximately 20%.

Understanding the landscapes and the elements that make up the landscapes can help us understand the entire natural ecosystems and biodiversity. Landscape ecology has been studied since the past. however, many studies are conducted on single landscapes, and comparative studies between landscapes are few. We compared insect species diversity and community structure within a single plant community across landscapes and habitat. Additionally, identify environmental factors that affect diversity. Our results showed that above-ground and below-ground insect communities were clearly distinguished. Additionally, species diversity was high below-ground in all landscapes. Insect community structures across landscapes did not differ in above-ground. However, below-ground, the urban was differentiated from the forest and agricultural land. We identified the urbanization indices GMIS and PHBASE as factors responsible for these difference.

The rate of resistant pest emergence has accelerated due to the continuous use of pesticides. Therefore, it is important to formulate insecticide resistance management measures and effective control methods for pest. Bemisia tabaci, a greenhouse pest, causes direct damage to crops such as growth inhibition and leaf discoloration at all developmental stages except for eggs. It also indirectly damages plants by secreting honeydew, which covers surrounding leaves and fruits, leading to sooty mold development. In this study, eight insecticides with high usage rates, categorized by their mode of action, were selected. Samples of Bemisia tabaci were collected from six regions, and resistance analysis were conducted. The results showed that Flonicamid exhibited a resistance ratio of 8.91 in Sejong, while Pyriproxyfen showed a high resistance ratio of 63.56 in Gunwi. Fluxametamide, Spinetoram, Cyantraniliprole, Dinotefuran, Pyridaben, and Milbemectin displayed resistance ratio ranging from 0.02 to 1.14 in most regions, except for Flonicamid and Pyriproxyfen.

The walking-stick insects, Ramulus mikado, are outbreaks in several mountainous areas from 2020 to 2022. In recent, some population of the insect are showed rapidly decline in their abundance, while some of them are still maintained high population density. In worldwide, insects belonging to Phasmida are reported to outbreak in their habitats as mentioned above environments, but knowledge about outbreak pattern of the walking-stick insects is still lacking. In this study, we aimed which biological and environmental factors are related to wax and wane of the insect population. From 2022 to 2023, we studied host tree preferences in natural conditions, ecological stoichiometry in major host trees, overwintering ecology of R. mikado eggs, and infection rate by entomophathogenic fungi during growing season.

This study was conducted to determine the appropriate seeding dates by verifying the difference in winter survival and productivity of alfalfa according to fall sowing dates in the central area of South Korea. The experiment was conducted for 2 years (2020 and 2021) at the field in the Department of Animal Resources Development, NIAS located in Cheonan. Sowing dates started from September 18 to November 8 with 10 days of intervals during 2020 and 2021; SO1 (September 18), SO2 (September 28), SO3 (October 8), SO4 (October 18), SO5 (October 28), and SO6 (November 8). After sowing, the winter survival rate was measured in the spring of the following year, and the dry matter yield was measured by harvesting at 10% flowering and harvesting five times a year. SO6 failed to winter survival, and SO5 also had a lower winter survival rate than SO1~4 (p<0.05). The average annual dry matter yield of alfalfa linearly decreased with delaying sowing dates (p<0.05). The feed value did not differ in the same year by delaying the sowing date in the same year. These results suggest that sowing date should be started before October 18 to increase winter survival and productivity of alfalfa in the central area of South Korea.

This qualitative case study explores multilingual learners’ linguistic practices and how they are interrelated with their identities in the context of a Korean alternative school. The learners are two Chosunjok, and one North Korean refugee child. The data were derived from the learners’ digital storytelling videos, semi-structured interviews, stimulated-recall interviews, and observation field notes. The data were thematically analyzed and organized using Rose’s (2007) sites of visual meaning-making structure. The findings revealed that the learners had different amounts of access to information regarding second language learning, and that they depended on the resources available within the communities they belonged to. Moreover, the participants’ levels of investment in language learning were constructed around their communities and identities. Their attitudes in language learning were also interrelated with the broader English language ideologies in South Korea. By sharing the stories of three multilingual learners, the study provides pedagogical implications on the influence of resources on multilingual learners’ language learning. We emphasize the importance of providing a space for multilingual learners to critically reflect on current and future resources, utilize their full communicative repertoire, and identify ways to increase their affordances of learning.

The spread of COVID-19 changes consumer preferences and behaviors greatly across the world. Extant literature has demonstrated that when there is a threat to disease, people stay away from those who do not seem healthy as they can be potentially infectious. Based on the previous literature, this research shows that individuals exposed to disease threat avoid products of which designs are high in visual complexity. When disease threat was present, individuals had lower purchase intention for products with complex designs. The perceived uncleanliness mediated the effect of visual complexity and disease threat on purchase intention. The findings provide a novel insight into the effect of disease salience on consumer perception of product design.

For the commercialization of hydrogen energy, a technology enabling safe storage and the transport of large amounts of hydrogen is needed. Porous materials are attracting attention as hydrogen storage material; however, their gravimetric hydrogen storage capacity (GHSC) at room temperature (RT) is insufficient for actual use. In an effort to overcome this limitation, we present a N-doped microporous carbon that contains large proportion of micropores with diameters below 1 nm and small amounts of N elements imparted by the nitrogen plasma treatment. The N-doped microporous carbon exhibits the highest total GHSC (1.59 wt%) at RT, and we compare the hydrogen storage capacities of our sample with those of metal alloys, showing their advantages and disadvantages as hydrogen storage materials.

The Animal and Plant Quarantine Agency conducts a targeted sampling plan and analysis for veterinary drugs within the country every year. Target compounds included tetrachlorvinphos as an organophosphate, diminazene as an anti-infective medication, ketoprofen as a nonsteroidal anti-inflammatory drug, triclabendazole and clorsulon as flukicides in 2022. These compounds were not included in National Residues Program (NRP), despite their high sales ranking. A total of 94 bovine muscle samples and 20 equine muscle samples were collected from various locations across the country. The analysis of target compounds in muscle was performed using LC-MS/MS coupled with Food code 8.3.1 revised in 2022. A 2 g sample of muscle tissue was extracted using a water: acetonitrile (1:4, v/v) solution, then cleaned up with C18 and hexane saturated with acetonitrile. Compounds were separated with C18 column and mobile phases consisted of 0.1% formic acid in water (A) and 0.1% formic acid in acetonitrile (B). All analytes exhibited good linearity with correlation coefficients (R2) higher than 0.992. The limit of quantification (LOQ) of these compounds ranged from 0.21 to 2.79 μg/kg except for diminazene (3.85~6.86 μg/kg). The average recoveries of these analytes were 89.45~129.13% in muscle at spiked level of 10 or 20 μg/kg. Relative standard deviations (%) (intra-day and inter-day) were lower than 20% for all target compounds, except for diminazene and triclabendazole, whose intra-day RSD % was slightly higher than 20% in equine muscle. Testing confirmed that all 94 bovine and 20 equine muscle samples from 9 provinces were free from residues of veterinary drugs. Monitoring of compounds not included in the NRP should continue to ensure consumer health and food safety.

Babesiosis is a tick-borne disease caused by intraerythrocytic protozoa. Despite the increasing acknowledgement that babesiosis represents a threat to animal and human health, to date there have been few studies focusing on the disease in the Republic of Korea (ROK). In the present study, we report a Babesia capreoli infection in an Ixodes nipponensis tick obtained from a Korean water deer (Hydropotes inermis argyropus). The tick was identified with polymerase chain reaction analysis as I. nipponensis (Japanese hard tick). A phylogenetic analysis based on the 18S rRNA gene sequences revealed that the isolate found in I. nipponensis belonged to the B. capreoli lineage and was distinct from the Asian, European, and North American lineages of Babesia divergens. Although our isolate belonged to the B. capreoli lineage it did not form a cluster with others isolates in the same lineage; this may be due to differences in the tick species that transmit B. capreoli or in the host species. We were unable to identify the reservoir host for our case of B. capreoli transmission, though regional ticks may be the primary vector. This study confirms the presence of B. capreoli in the ROK, and its presence suggests that further study is warranted to determine its prevalence and pathogenicity in wild and domesticated animals.

Macrophages secrete various cytokines and inflammatory mediators, resulting in playing critical roles in inflammation and immunity. In this study, we investigated anti-inflammatory and immune enhancing properties of PB203, which is a water-soluble extract powder from the fruit of Actinidia polygama, in macrophages. A. polygama is a medicinal plant traditionally known to treat abdominal pain, stroke and rheumatoid arthritis. However, the molecular mechanism for the immune modulation of PB203 is still unclear. Therefore, we assessed the effects of PB203 on the lipopolysaccharide (LPS)-induced inflammation and immune activation, and elucidated its action mechanism in mouse macrophage, RAW264.7 cells. PB203 significantly suppressed not only the levels of nitric oxide (NO), prostaglandin E2, tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β), but also the mRNA expression of inducible NO synthase, cyclooxygenase-2, TNF-α and IL-1β in LPS-stimulated RAW264.7 cells. We also found that these anti-inflammatory activities of PB203 were mediated through the inhibition of toll-like receptor 4 and nuclear factor kappa B (NF-κB) induced by LPS. On the other hand, in normal macrophages, PB203 dose-dependently elevated the gene expression of immunomodulators including granulocyte-macrophage colony-stimulating factor, granulocyte colony-stimulating factor, monocyte chemoattractant protein-1 and TNF-α in a statistically significant manner. The expression of IL-10, IL-1β, IL-6, and interferon-γ were also remarkably upregulated by the treatment of 500 μg/mL PB203. In addition, PB203-mediated production of NO and TNF-α was attenuated by NF-κB inhibition in RAW264.7 cells. Interestingly, PB203 promoted the production of nuclear factor erythroid-2-related factor 2, resulting in the increased level of heme oxygenase-1, which is a representative antioxidant enzyme, in both LPS-stimulated and normal RAW264.7 cells. Taken all together, these results suggest that PB203 may have great potential as the candidate of anti-inflammatory agent for improving inflammatory diseases or immune enhancing agent for preventing infectious diseases. Keywords: Actinidia polygama extract (PB203); macrophages; immunomodulator; nuclear factor kappa B (NF-κB); heme oxygenase-1 (HO-1)

Polymeric carbon nitride (p-C3N4) is a promising platform as a metal-free photo-catalyst for various reactions. The p-C3N4 can be produced by thermal poly-condensation of organic precursors. Their morphological and chemical structures depend on reaction conditions during the poly-condensation. In this study, two p-C3N4 materials are produced by heat treatment of urea under different gaseous conditions with air (urea-derived carbon nitride under air, UCN-A) and N2 (UCN-N), respectively. UCN-A and UCN-N samples are mesoporous materials and show excellent photocatalytic activities for degrading rhodamine B, an organic pollutant, under the irradiation of visible light. The UCN-A shows the better photocatalytic activity than UCN-N. Various characterizations reveal that more porous structures and larger surface areas of UCN-A are reasons for the better photocatalytic performance.

Zirconium(Zr) alloys are commonly used in the nuclear industry for applications such as fuel cladding and pressure tubes. To minimize the levels and volumes of radioactive waste, molten salts have been employed for decontaminating Zr alloys. Recently, a two-step Zr metal recovery process, combining electrolysis and thermal decomposition, has been proposed. In the electrolysis process, potentiostatic electrorefining is utilized to control the chemical form of electrodeposits(ZrCl). Although Zr metals are expected to dissolve into molten salts, reductive alloy elements can also be co-dissolved and deposited on the cathode. Therefore, a better understanding of the anodic side’s response during potentiostatic electrorefining is necessary to ensure the purity of recovered Zr and long-term process operation. As the first step, potentiodynamic polarization curves were obtained using Zr, Nb, and Zr-Nb alloy to investigate the anodic dissolution behavior in the molten salts. Nb, which has a redox potential close to Zr, and Zr exhibit active or passivation dissolution mechanisms depending on the potential range. It was confirmed that Zr-Nb alloy also has a passivation region between -0.223 to -0.092 V influenced by the major elements Zr and Nb. Secondly, active dissolution of Zr-Nb was performed in the range of -0.9 to -0.6 V. The dissolution mechanism can be explained by percolation theory, which is consistent with the observed microstructure of the alloy. Thirdly, passivation dissolution of Zr, Nb, and Zr-Nb alloy was investigated to identify the pure passivation products and additional products in the Zr-Nb alloy case. K2ZrCl6 and K3NbCl6 were identified as the pure passivation products of the major elements. In the Zr-Nb alloy case, additional products, such as Nb and NbZr, produced by the redox reaction of nanoparticles in the high viscous salt layer near the anode, were also confirmed. The anodic dissolution mechanism of Zr-Nb alloy can be summarized as follows. During active dissolution, only Zr metal dissolves into molten salts by percolation. Above the solubility near the anode, passivation products begin to form. The anode potential increases due to the disturbance of passivation products on ion flow, leading to co-dissolution of Nb. When the concentration of Nb ion exceeds the solubility, a passivation product of Nb also forms. In this scenario, a high viscous salt layer is formed, which traps nanoparticles of Zr metal, resulting in redox behavior between Zr metal and Nb ion. Some nanoparticles of Zr and Nb metal are also present in the form of NbZr.