Radiation from spent nuclear fuel (SNF) is one of key factors affecting the dissolution process of SNF and the source term from repository. The dissolution rate of uranium dioxide (UO2) matrix of SNF is expected to control the release of radionuclides from SNF in contact with water under geological disposal conditions. Based on the oxidative dissolution mechanism, the solubility of UO2 can increase significantly if the reducing environment near the fuel surface is altered by water radiolysis caused by radiation from SNF. Therefore, the analysis of water radiolysis products such as radicals (·OH, ·OH2, eaq, ·H) and molecules (H3O+, H2, H2O2) is perquisite for studies on the rate of such dissolution process to determine oxidation/dissolution mechanism and related rate constants. In this study we examined the two-known spectroscopic methods developed for H2O2 determination; one is the luminol-based chemiluminescence (luminol-CL) method and the other is the spectrophotometry using ferrous oxidation-xylenol orange complexation (FOX). Their applicability for quantitative analysis of H2O2 in potential aqueous samples from SNF dissolution studies was evaluated in terms of the analytical dynamic range (ADR), the limit of detection (LOD) and the interfering effects of various metal ions possibly present in real samples. The luminol-CL method exploits the chemiluminescence reaction caused by luminol; when in the presence of a metallic catalyst (e.g., Cu2+, Co2+), luminol emits a blue light (425 nm) at pH 10- 11 in response to oxidizing agents such as hydrogen peroxide. Although a flow-through reaction system is routinely employed to enhance the analytical sensitivity we achieved the ADR up to ~200 μM and LOD < 1 μM by a batch-wise CL detection using conventional cuvette cells and an intensified charge-coupled device (ICCD). Interestingly, it turned out that the interfering effects of other metal ions (e.g., UO2 2+, U4+, Fe2+ and Fe3+) is minimal, which should be advantageous for the luminol-CL method to be employed for samples potentially containing other metal ions. On the other hand, the FOX method spectrophotometrically analyzes H2O2 based on the difference in color (or absorption spectra) of Fe-xylenol orange (XO) complexes. Initially, the Fe2+-XO complex was provided in working solutions at pH 3, which was subsequently mixed with samples having H2O2 and allowed for quantitative oxidation of Fe2+ to Fe3+. Typically, by monitoring the absorbance of Fe3+-XO complex at 560-580 nm (λmax) the ADR up to ~100 μM and LOD ~1.6 μM were achieved. However, it is found that interfering effects from M3+ and M4+ ions are significant; these interfering metal ions can form XO complexes so as to directly contribute the measured absorbance. In contrast, the influence from M2+ ions was found to be negligible. To summarize we conclude that both methods can be applied for H2O2 determination for aqueous samples taken from SNF dissolution tests. However, prior to applying the FOX method the metal ion composition in those samples should be thoroughly identified not to overestimate the H2O2 concentration of samples. More details of underlying chemical reactions in both methods will be discussed in the presentation.

Spent ion exchange resins have been generated during the operation of nuclear facilities. These resins include radioactive nuclides. It is needed to fabricate them into a stable form for final disposal. Cement solidification process is a useful method for the fabrication of them into a waste form for final disposal. In this study, proper conditions for the fabrication of them into a stable waste form were determined using the cement solidification process. In-drum waste forms were then produced at the conditions, where the stability of representative samples was evaluated for final disposal. The samples were satisfied to the Waste Acceptance Criteria for low and intermediate level radioactive waste disposal sites. This result can be utilized to derive optimal conditions for the fabrication of spent ion exchange resins into a final disposal form.

The post-closure safety assessment of a repository is typically conducted over an extensive timescale from ten thousand to a million years. Considering that biosphere ecosystems may undergo significant changes over such lengthy periods, it is essential to incorporate the long-term evolution of the biosphere into the safety assessment. Climate change and landscape development are identified as critical drivers with the potential to impact the hydrogeological and hydrogeochemical characteristics of the biosphere. These changes can subsequently alter the migration patterns of radionuclides through the biosphere and influence human exposure doses. Therefore, this study formulates scenarios within the context of long-term biosphere evolution. We examine biosphere assessment processes employed in other countries and conduct a comparative study on scenario conditions. For example, biosphere assessment in Finland has identified sea-level changes and land-use alterations as significant factors in the long-term evolution of the biosphere. These factors are linked to Features, Events, and Processes (FEPs) associated with climate change and human activities. Sea-level changes are related to FEPs regarding climate change, land uplift, and shoreline displacement, while land-use changes are based on human activity-related FEPs (e.g., crop type, livestock and forest management, well construction, and demographics). Based on the literature review, this study has configured long-term evolution scenarios for the safety assessment of a deep geological repository for spent fuels.

Safety assessments for geological disposal systems extend over tens of thousands of years, taking into account the radiotoxicity decay period of spent nuclear fuel. During this extensive period, the biosphere experiences multiple glacial cycles, and fluctuations in seawater amounts, attributed to the formation and melting of glaciers, lead to global sea level changes known as eustacy. These sea level changes can directly influence the land-sea interface and groundwater flow dynamics, consequently affecting the pathways of radionuclide transport - an essential element of dose assessment. Therefore, this study aims to investigate how glacial cycles and sea level changes impact radionuclide transport within geological disposal systems, especially in the biosphere. To achieve this objective, we obtained climate evolution data including sea level changes for the Korean Peninsula over a 200,000-years, simulated by a General Circulation Model (GCM). These data were then employed to predict site and hydrology evolutions. The study site was conceptualized biosphere of Artificial Disposal System (ADioS), and we utilized the Soil and Water Assessment Tool (SWAT) to simulate hydrological evolution. These datasets, encompassing climate, site, and hydrology evolution, were collectively employed as inputs for the biosphere module of Adaptive Process-Based Total System Performance Assessment Framework (APro). Subsequently, the APro’s biosphere module calculated radionuclide transport in groundwater flow and its release into surface water bodies, considering the influences of glacial cycles and sea level changes. The results show that hydrologic changes due to sea level change are relatively minor, while the impact of sea level change on groundwater flow and discharge is significant. Additionally, we identified that among the water bodies within ADioS, including rivers, lakes, and oceans, the ocean exhibits the most substantial radionuclide outflow throughout the entire period. The spatiotemporal distributions of radionuclides computed within APro will be further processed into a grid format and used as input for the dose assessment module. Through this study, it was possible to determine the impact of long-term glacial cycles and sea level changes on radionuclide transport. Additionally, this module can serve as a valuable tool for providing the spatiotemporal variability of radionuclides required for enhanced dose assessments.

The Korea Atomic Energy Research Institute (KAERI) is currently developing a process-based performance assessment model known as APro. Distinguished from the previous system-level safety assessment model developed by KAERI, APro exhibits the capacity to encompass a threedimensional biosphere domain, evolving over the long term. In this study, we elucidate the methodology employed in developing the dose assessment module of APro and present the module’s functionalities. The procedural steps underlying radiation dose calculations within the APro framework can be succinctly outlined as follows: 1) Definition of a landscape model, utilizing information derived from a specified snapshot period provided by the APro biosphere transport module; 2) Generation of unit biotope objects spanning the landscape; 3) Evaluation of radionuclide transfer within the soil medium; 4) Calculation of activity concentration for flora and fauna groups; 5) Assessment of the distribution of effective dose among representative human groups; 6) Progressing through successive time steps. The APro dose calculation module exhibits notable capabilities that encompass: 1) Accounting for radionuclide decay and ingrowth; 2) Facilitating transfer through unsaturated porous media; 3) Considering sorption effects; 4) Addressing the inheritance of radioactivity between various landscape models; 5) Offering customizable ecosystem parameters; 6) Providing flexibility for user-defined exposure pathways. Leveraging these functionalities of the dose assessment module, APro is proficient in evaluating the distribution of radiological doses and associated risks for representative population groups, all while accounting for the dynamic, long-term evolution of the biosphere, including alterations in land cover.

Copper, mainly used as a material for outer canister, generates various corrosion products under aerobic and anaerobic conditions in the operational and/or post-closure phases of the deep geological repository. These products could affect performance of engineering barrier system (EBS) through interaction with surrounding bentonite that makes up the buffer and backfill materials. Accordingly, in this study, we suggested research items to be conducted to minimize degradation of EBS due to copper corrosion products, based on the phenomenological review results for copper corrosion mechanisms and interaction between resultant product and bentonite in the deep geological disposal environment. During the post-closure phase, condition in the disposal facility changes form aerobic to anaerobic over time, and thereby, causes and products of copper corrosion vary. Under aerobic condition, copper corrosion is mainly induced by oxygen (O2) in the repository, chloride (Cl-) and carbonate (CO3 2-) ions from groundwater flowing into the facility, resulting in corrosion products such as cuprite (Cu2O), tenorite (CuO), atacamite (CuCl2·3Cu(OH)2) and malachite (Cu2CO3(OH)2). And, copper corrosion under anaerobic condition is primarily due to hydrogen sulfide (H2S) and sulfate (SO4 2-) in groundwater flowing into the facility, leading to formation of chalcocite (Cu2S) and covellite (CuS) as corrosion products. Depending on environment of the disposal facility, copper corrosion products are dissolved and ionized to Cu2+ in groundwater, and subsequently adsorbed on the nearby smectite. Then, it causes a cation exchange reaction with exchangeable cations in the interlayer of smectite. As a result of reviewing the previous experiments, it was confirmed that Cu2+-exchanged bentonite has a slightly reduced basal spacing and swelling capacity. From the results as above, there is a possibility that performance of EBS may be degraded due to copper corrosion products. To minimize its effect of degradation in the domestic facility, items to be further studied are as follows: (a) Method for reducing copper corrosion such as selection of appropriate material and structure for the canister, and (b) How to control dissolution of copper canister product into groundwater through predicting type and ionization process. The results of this study could be directly used to developing design concept of EBS for the domestic disposal facility and to establishing roadmap of future R&D programs.

As a promising anode for sodium-ion batteries (SIBs), cobalt sulfide ( CoS2) has attracted extensive attention due to its high theoretical capacity, easy preparation, and superior electrochemical activity. However, its intrinsic low conductivity and large volume expansion result in poor cycling ability. Herein, nitrogen-doped carbon-coated CoS2 nanoparticles (N–C@ CoS2) were prepared by a C3N4 soft-template-assisted method. Carbon coating improves the conductivity and prevents the aggregation of CoS2 nanoparticles. In addition, the C3N4 template provides a porous graphene-like structure as a conductive framework, affording a fast and constant transport path for electrons and void space for buffering the volume change of CoS2 nanoparticles. Benefitting from the superiorities, the Na-storage properties of the N–C@CoS2 electrode are remarkably boosted. The advanced anode delivers a long-term capacity of 376.27 mAh g− 1 at 0.1 A g− 1 after 500 cycles. This method can also apply to preparing other metal sulfide materials for SIBs and provides the relevant experimental basis for the further development of energy storage materials.

We produced an activated carbon using sodium-lignosulfonate, in which we investigated how the sodium salt in lignin served as the activating agent during heat treatment. Our process resulted in a product with a high specific surface area of 1324 m2/ g at 800 °C and microporous structure. During the activation process, we observed the consumption of carbon due to the dehydration reaction of NaOH and the reduction of Na2CO3 to metallic Na, which created pores through oxidation/ reduction reactions. The intercalation of metallic Na between the lattices at high temperatures formed additional pores and increased the specific surface area. Our proposed mechanism holds promise for enhancing the control of the microstructure and porosity of activated carbons through the thermal treatment of biomass.

A novel kind of self-assembled graphene quantum dots-Co3O4 (GQDs-Co3O4) nanocomposite was successfully manufactured through a hydrothermal approach and used as an extremely effectual oxygen evolution reaction (OER) electrocatalyst. The characterization of morphology with scanning electron microscopy (SEM) and transmission electron microscopy (TEM) showed that Co3O4 nanosheets combined with graphene quantum dots (GQDs) had a new type of hexagonal lamellar selfassembly structure. The GQDs-Co3O4 electrocatalyst showed enhanced electrochemical catalytic properties in an alkaline solution. The start potential of the OER was 0.543 V (vs SCE) in 1 M KOH solution, and 0.577 V (vs SCE) in 0.1 M KOH solution correspondingly. The current density of 10 mA cm− 2 had been attained at the overpotential of 321 mV in 1 M KOH solution and 450 mV in 0.1 M KOH solution. Furthermore, the current density can reach 171 mA cm− 2 in 1 M KOH solution and 21.4 mA cm− 2 in 0.1 M KOH solution at 0.8 V. Moreover, the GQDs-Co3O4 nanocomposite also maintained an ideal constancy in an alkaline solution with only a small deterioration of the activity (7%) compared with the original value after repeating potential cycling for 1000 cycles.

With the advancement and diversification of the bread industry, eco-friendly products with less sugar and salt, and containing functional ingredients are being developed. To develop healthy bread, Korean pine leaf powder was added in different proportions (0%, 1%, 3%, 5%, and 7%), and the quality characteristics of the bread, namely height, moisture, color value, texture, antioxidant property, and sensory characteristics were evaluated. As the amount of leaf powder was increased in the bread, L-value in the range of 53.45~85.05 (p<0.001) and adhesiveness in the range of 0.13~0.32 mJ (p<0.001) decreased significantly, whereas b-value in the range of 16.75~30.74 (p<0.001), total polyphenol content in the range of 466.83~669.13 ug/mL, ABTS- in the range of 0.46~43.23%, DPPH-radical in the range of 1.39~45.76%, scavenging capacities (p<0.001), color in the range of 3.27~5.40 (p=0.017) and texture in the range of 4.33~4.80 (p=0.006) preferences increased significantly. This study could increase the utilization of Korean pine leaf and the production of healthy food with antioxidant properties.

VRFB에 사용되는 막의 수송 능력은 배터리 성능에 필수적인 요소이다. 탁월한 배터리 성능을 위해서는 높은 양 성자 전도도와 낮은 바나듐 이온 투과도가 달성되어야 한다. 하지만 양성자 전도도와 바나듐 이온 투과도 사이에는 상충관계 가 존재한다. 따라서 이 상충관계를 해결하는 것이 VRFB의 발전에 필수적이다. 또한 높은 쿨롱 효율, 전압 효율 및 에너지 효율을 유지하는 것이 고성능 VRFB를 위해 필수적이다. 최근 복합막과 SPEEK 막을 중심으로 나피온 막의 기존 한계를 극 복하기 위한 다양한 시도가 이루어지고 있다. VRFB은 이 논문에서 검토하는 복합막에서 충전식 배터리의 필수 등급이다.

PURPOSES : A model for minimizing cutting loss and determining the optimum layout of blocks in pavements was developed in this study. METHODS : Based on literature review, a model which included constraints such as the amount, volume, overlap, and pattern, was developed to minimize the cutting loss in an irregular pavement shape. The Stach bond, stretcher bond, and herringbone patterns were used in this model. The harmony search and particle swarm algorithms were then used to solve this model. RESULTS : Based on the results of the model and algorithms, the harmony search algorithm yielded better results because of its fast computation time. Moreover, compared to the sample pavement area, it reduced the cutting loss by 20.91%. CONCLUSIONS : The model and algorithms successfully optimized the layout of the pavement and they have potential applications in industries, such as tiling, panels, and textiles.