The operation of nuclear facilities involves the potential for on-site contamination of soil, primarily resulting from pipe leaks and other operational incidents. Globally, decommissioning process for commercial nuclear power plants have revealed huge-amounts of soil waste contaminated with Cs-137, Sr-90, Co-60, and H-3. For example, Connecticut Yankee in the United States produced approximately 52,800 ton of contaminated soil waste, constituting 10% of the total waste generated during its decommissioning. Environmental remediation costs associated with nuclear decommissioning in the US averaged $60 million per unit, representing a significant 10% of the whole decommissioning expenses. Consequently, this study undertook a preliminary investigation to identify important factors for establishing a site remediation strategy based on radionuclide- and site-specific media- characteristics, focusing the efficiency enhancement for the environmental remediation. The factors considered for this investigation were categorized into physical/environmental, socioeconomic, technical, and management aspects. Physical/environmental factors contained the site characteristics, contamination levels, and environmental sensitivity, while socio-economic factors included the social concerns and economic costs. Technical and management factors included subcategories such as technical considerations, policy aspects, and management factors. Especially, technical factors were further subdivided to consider the site reuse potential, secondary waste generation by site remediation, remediation efficiency, and remediation time. Additionally, our study focused the key factors that facilitate the systematic planning for the site remediation, considering the distribution coefficient (Kd) and hydrogeological characteristics associated with each radionuclide in specific site conditions. Therefore, key factors in this study focus the geochemical characteristics of site media including the particle size distribution, chemical composition, organic and inorganic constituents, and soil moisture content. Moreover, the adsorption properties of site media were examined concerning the distribution coefficient (Kd) of radionuclides and their migration characteristics. Furthermore, this study supported the development of a conceptual framework, containing the remediation strategies that incorporate the mobility of radionuclides, according to the site-specific media. This conceptual framework would necessitate the spatial analysis techniques involving the whole contamination surveys and radionuclide mobility modeling data. By integrating these key factors, the study provides the selection and simulation of optimal remediation methods, ultimately offering the estimated amounts of radioactive waste and its disposal costs. Therefore, these key factors offer foundational insights for designing the site remediation strategies according the sitespecific information such as the distribution coefficient (Kd) and hydrogeological characteristics.

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.

Pt/C catalysts were prepared using black carbon (CB), and evaluated for their potential application as a catalyst of liquid-phase catalystic exchange for tritium treatment. CB was treated with 10% H2O2 solution for 0 and 2 hours at 105°C, Ethylene glycol and 40wt% Pt were added to the dried treated sample to prepare a Pt/C catalyst. The physical and chemical properties of the prepared catalysts were evaluated by BET, XRD, elemental analysis (EA), and TEM analyses. As a result of BET analysis, the surface area of CB without 10% H2O2 was 237.2 m2·g-1, and after treatment with 10% H2O2, it decreased to 181.2 m2·g-1 for 2 hours. However, the internal surface area increased, indicating the possibility that more Pt could be distributed inside the CB treated with 10% H2O2. In the XRD analysis results, the presence of Pt was confirmed by observing the Pt peak in the prepared Pt/C catalyst, and it was also observed through TEM analysis that Pt was evenly distributed within the CB. The elemental analysis (EA) results showed that the ratio of S and N decreased and the ratio of O increased with increasing 10% H2O2 treatment time. The H2O2 treated carbon supported Pt catalysts and polytetrafluoroethylene were then loaded together on a foamed nickel carrier to obtain hydrophobic catalysts. Our hydrophobic Pt catalyst using H2O2 treated black carbon are expected to be usefully used in the tritium treatment system.

Hydrogen isotope separation involves the separation of hydrogen, deuterium, tritium, and their isotopologues. It is an essential technology for removing radioactive tritium contamination and for obtaining valuable hydrogen isotope resources. Among various hydrogen isotope separation technologies, water electrolysis technology exhibits a high separation factor. Consequently, the electrolysis of tritiated water is of paramount importance as a tritium enrichment method for treating tritium-contaminated water and for analyzing tritium in environmental samples. More recently, hydroelectrolysis technology, which utilizes proton exchange membranes (PEM) to reduce water inventory, has gained favor over traditional alkaline hydroelectrolysis. Nevertheless, it is crucial to decrease the hydrogen permeability of the PEM in order to mitigate the explosion risk associated with tritium hydrogen electrolysis devices. Additionally, efforts are needed to enhance the hydrogen isotope selectivity of the PEM and optimize the manufacturing process of the membrane-electrode assembly (MEA), thereby improving both hydrogen isotope separation performance and water electrolysis efficiency. In this presentation, we will delve into two key aspects. Firstly, we’ll explore the reduction of hydrogen permeability and the enhancement of the hydrogen isotope separation factor in PEM through the incorporation of 2D nanomaterial additives. Secondly, we’ll examine the influence of various MEAs preparation methods on electrolysis and isotope separation performances. Lastly, we will discuss the effectiveness of the developed system in separating deuterium and tritium.

해충에 이용되는 화학적 기피제는 생태계를 파괴할 수 있으며 내성을 가진 생물체로의 진화를 촉진한다. 같은 종의 생물끼리의 의사소통 수단인 페로몬을 이용하면 다른 종에게 영향을 미치지 않으면서 특정 곤충에 특이적 으로 작용하는 방충제를 제작할 수 있을 것이라 생각된다. 본 연구는 초파리(Drosophila)의 페로몬 2종류를 추출 하여 초파리의 기피도 및 유인도와 번식률을 확인하고자 한다. ℃, 광주기 12h/12h의 동일한 조건에서 사육하 며 10마리당 헥세인 10를 사용하여 암컷의 표피에서 CHC 페로몬과 수컷의 페로몬샘에서 cVA 페로몬을 추출 한다. 연령, 성별, 교배 여부에 따라 관찰통에 각각의 페로몬을 처리하여 지정구간에 분포하는 초파리의 수를 계수하여 기피도 및 유인도를 확인한다. 관병에 암수 1쌍을 투입하고 하루에 1번 선정한 페로몬을 투여하며 산란 수을 측정한다. 이 연구를 통해 CHC가 수컷 초파리에 대한 기피 효과가 있음을 확인하였으며 추출되는 수컷의 연령이 높을수록 cVA에 의한 번식률 감소가 크게 나타났다. 본 연구를 통해 페로몬을 통한 초파리의 방제 가능성 을 확인하였으므로 다른 곤충의 방제에도 적용할 수 있을 거라 기대한다. 페로몬은 생물 농축과 같은 환경적 영향이 없으며 소량으로 유의미한 결과를 도출했다는 점에서 의의가 있으며 상용화를 통해 해충에 의해 피해를 해결할 수 있을 것이라 기대한다.

The separation of hydrogen isotopes is a critical issue in various fields, such as deuterium or tritium production and the treatment of radioactively contaminated water. In this presentation, we describe the pervaporative separation of hydrogen isotopes using proton conductive membranes and underlying separation mechanism. We investigated the H/D separation factors of perfluorosulfonic acid (Nafion) and polybenzimidazole membranes using pervaporation, and found that both membranes exhibited similar separation factors of approximately 1.026. Water permeation flux through the membranes was highly dependent on their thickness and type, and increased with operation temperature. However, the effect of temperature on H/D separation factor was negligible. We also demonstrated the cascade separation of H/D, indicating the potential application of multi-stage operation. We found that surface transport mechanisms such as hydron hopping contributed the most to H/D separation during the pervaporation process of proton conductive membranes.

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. This study have the literature review for previous research on D2/H2 adsorption and analyzes the D2/H2 adsorption behaviors of hydrogen isotopes for various zeolite using BET at 77 K. The study predicts the D2/H2 adsorption selectivity based on the results obtained with BET. These hydrogen isotope adsorption fundamentals provide a foundation for future processes for tritium separation.

Water electrolysis is an efficient method to enrich heavy hydrogen isotopes (tritium and deuterium) in the aqueous phase. Although an alkaline water electrolyzer has been commercialized for mass production of hydrogen, such a method requires additional purification steps to remove electrolytes from the final concentrates. On the other hand, proton exchange membrane water electrolysis (PEMWE) does not require additional electrolyte treatment steps, and PEMWE is operated at higher current density compared to the alkaline water electrolysis. In this study, we investigated deuterium and tritium separation from light water by PEMWE. Separation behaviors at the anode and cathode were analyzed, and H/D and H/T separation factors were compared.

Hydrogen isotopes (H, D, T) separation technologies have received great interest for treatments of tritiated liquid waste produced in Fukushima. In addition, the separated deuterium and tritium can be utilized in various industries such as semiconductors and nuclear fusion as expensive and rare resources. However, separating hydrogen isotopes in gas and liquid forms still requires energyintensive processes. To improve efficiency and performance of hydrogen isotope separation, we are developing water electrolysis, cryosorption, distillation, isotope exchange, and hydrophobic catalyst technologies. Furthermore, an analytical method is studied to evaluate the separation of hydrogen isotopes. This presentation introduces the current status of hydrogen isotope research in this research group.

Water electrolysis is a representative technology for tritium enrichment in water. Proton exchange membrane (PEM) water electrolysis has received great attention to replace traditional alkaline water electrolysis which generates concentrated tritiated water containing a large amount of salts. Nafion has been widely used as a polymeric electrolyte for the PEM electrolyzer. However, its low gas barrier property causes explosion, corrosion or degradation of electrolyzer. Furthermore, the traditional polymeric electrolytes have negligible differences in conductivity between hydrogen isotopes. To enhance the tritium separation by water electrolysis, we designed a composite membrane (Nafion/ hexagonal boron nitride (hBN)). The monolayer hBN has a high proton conductivity and gas barrier property, and the hBN can enhance conductivity differences between hydrogen isotopes. We prepared Nafion/hBN composite membranes, and water electrolysis performances and proton/deuterium separation behaviors were investigated.

Detritiation of low-level tritiated water has become global issue after Fukushima accident. Several attempts have been made to reduce the radioactivity of Fukushima tritiated water below legal limit of nuclear plant effluents (~104 Bq·L−1). Various technologies such as water distillation, electrolysis, and catalytic exchange were tested to treat the tritiated water, however, those demand enormous expense to achieve the goal due to low process efficiency. It highlights that the performance enhancement of current technologies is necessary to improve economic feasibility. We have quantitatively evaluated the separation performance of various polymers toward low-level tritium (~105 Bq·L−1) through batch experiments. The polystyrene with grafted by 20 types of functional groups (Tris (2-aminoethyl) amine, dimethylaminomethyl, isocyanate, mercaptomethyl, aminomethyl, hydroxymethyl, triphenylphosphine, morpholine, 2-chlorotrityl amine, 4-(dimethylamino) pyridine, poly (vinyl chloride) carboxylated, poly (4-vinyl pyridine), p-toluenesulfonic acid, p-toluenesulfonyl hydrazide, piperidine, acetyl polystyrene, 2-chlorotrityl chloride, piperazine, diethylene triamine, poly (vinyl chloride)) were suspended in HTO solution (initial activity = 4.7 × 105 Bq·L−1). After the equilibration, the suspension was filtered using 3 kDa membrane filter and the activity in filtrates were quantified by LSC (HIDEX-300 SL). The results demonstrate the detritiation efficiency and separation factors of functional groups toward tritium. Carboxylic group (COOH) showed the most reactive performance as detritiation efficiency of ~4%. Compared to other functional groups, styrene sulfonyl groups including sulfonyl amide (SNH2) and sulfonyl hydrazide (SNHNH2) revealed promising performance for tritium separation as separation factor of 10.97 and 3.85, respectively. However, sulfonyl hydroxide (SOH) which is known as reactive functional group to tritium exchange showed the poor performance (detritiation efficiency: 0.68%; separation factor: 3.02). This study could suggest the promising functional groups for detritiation of low-level tritiated water which can be utilized to enhance the performance of current technologies. For example, reactive functional groups can be grafted on the surface of packing material within distillation tower resulting in the increasing detritiation efficiency.

The behaviors of various desorption agents were investigated during the desorption of cesium (Cs) from samples of clay minerals and actual soil. Results showed that polymeric cation exchange agents (polyethyleneimine (PEI)) efficiently desorbed Cs from expandable montmorillonite, whereas acidic desorption solutions containing HCl or PEI removed considerable Cs from hydrobiotite. However, most desorption agents could desorb only 54% of Cs from illite because of Cs’s specific adsorption to selective adsorption sites. Cs desorption from an actual soil sample containing Cs-selective clay mineral illite (< 200 μm) and extracted from near South Korea’s Kori Nuclear Power Plant was also investigated. Considerable adsorbed 137Cs was expected to be located at Cs-selective sites when the 137Cs loading was much lower than the sample’s cation exchange capacity. At this low 137Cs loading, the total Cs amount desorbed by repeated washing varied by desorption agent in the order HCl > PEI > NH4+, and the highest Cs desorption amount achieved using HCl was 83%. Unlike other desorption agents with only cation exchange capabilities, HCl can attack minerals and induce dissolution of metallic elements. HCl’s ability to both alter minerals and induce H+/Cs+ ion exchange is expected to promote Cs desorption from actual soil samples.