Facing the decommissioning era of nuclear facility, it is necessary to develop technology for treating wastewater containing nuclides. Among variety of nuclides, Cs/Sr/Co are the major nuclides considering quantity and radioactivity. In this presentation, we report the performance of nanofiltration and reverse osmosis membranes for nuclides separation. Reverse osmosis membranes have quite effective for the separation of Cs, Sr, and Co. Rejection is above 93% for single component and even higher for mixed nuclides separation, > 98%. This study indicates that polymeric membranes can be potential candidate for nuclides separation.

Heavy metal ion separation of commercial polymeric membranes is investigated to elucidate the permeation mechanism and possibility on applying treatment of wastewater from various origins. Since wastewater contains significant amount of heavy metal ions, their treatment to recycle or reuse is necessary. Polyamide based commercial membranes are prepared to test their separation performance on single- & multi-component heavy metal aqueous solutions. This study indicates that polymeric membranes can be potential candidate for heavy metal separation.

Nuclide separation of commercial nanofiltration (NF) & reverse osmosis (RO) membranes is investigated to elucidate the permeation mechanism and possibility on applying treatment of wastewater from nuclear facility. Since wastewater from nuclear facility contains significant amount of dangerous nuclides, their treatment for recycle or clearance is necessary. Polyamide based commercial membranes are prepared to investigate their separation performance on single- & multi-component nuclide aqueous solutions. Similar to their desalination performance, NF shows higher flux, but RO has high rejection. With respect to rejection, NF and RO membranes have better performance comparing to desalination. This study indicates that NF and RO membranes can be potential candidate for nuclide separation.

Membrane-based gas separations are becoming relevant. Ordered mesoporous silicas have uniform pore channels with a mesopore range. The mesopores are advantageous for rapid diffusion of target molecules, can be modified in a variety of ways, allowing for separation applications. We first describe the technologically scalable fabrication based upon mesoporous silica membranes on polymeric hollow fibers. Furthermore, we modify the mesopores using amine-containing polysilsesquioxane molecules. The resulting modified membranes exhibit promising permeability and selectivity in separation of CO2 from N2 or CH4. Also, the CO2 and N2 transport properties of aziridine-functionalized mesoporous silica membranes are investigated. The hyperbranched aminosilica membrane shows bi-functional gas transport property regarding humidity of gas streams.

Radioactive liquid waste has given soil & water pollution and further congenital defect to the humanity. With this regard, there are lots of interests in reducing concentration of radioactive material even if it is in low level (ppm). There are filtration driven by pressure such as ultra-filtration, nano-filtration, and reverse osmosis to separate radioactive liquid waste. Among them, Nano-Filtration membrane shows promising performance in both permeability and selectivity. Commercial nanofiltration membrane were applied to separate model solutions. Model seawater was desalinated to 6,100 ppm with flux of 90 L/ ㎡h. On the other hands, Model nuclides (Co, Cs, and Sr) solutions are separated from 10 ppm to 2 ppm, 0.23 ppm, and 0.13 ppm. Commercial nanofiltration membranes show the trade-off property between selectivity and flux.

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.

Tritium is radioactive isotope, emitting beta ray, released as tritiated water from nuclear power plants. Due to the danger of radioactive isotope, the appropriate separation of tritium is essentially carried out for environment and safety. Further, it is also promising material for energy production and research. The tritiated water can be treated by diverse techniques such as water distillation, cryogenic distillation, Girdler-sulfide process, and catalytic exchange. After treatment, it is more desirable to convert as gas phase for storage, comparing to liquid phase. However, achieving complete separation of hydrogen gases with very similar physical and chemical properties is significantly challenging. Thus, it is necessary to develop materials with effective separation properties in gas separation. In this presentation, we present hydrogen isotope separation in the gas phase using modified mesoporous silica. Mesoporous silica is a form of silica that is characterized by its mesoporous structure possessing pores that range from 2 to 50 nm in diameter. This material can be functionalized to selectively capture and separate molecules having specific size and affinity. Here, the silver and copper incorporated mesoporous silica was synthesized to tailor a chemical affinity quantum sieving effect, thereby providing separation efficiency in D2/H2. The adsorption quantities of H2 and D2 were determined by sorption study, and the textural properties of each mesoporous silica were analyzed using N2 physisorption. The selectivity (D2/H2) in diverse feed composition (1:1, 1:9, and 1:99 of D2/H2) was estimated by applying ideal adsorbed solution theory to predict the loading of the gas mixture on bare, Ag- and Cu-mesoporous silica based on their sorption study. Further, the performance of each mesoporous silica was evaluated in the breakthrough adsorption under 1:1 mixture of D2 and H2 at 77 K.

Carbon 14 (14C) is radioactive isotope of carbon which emits beta ray with long half-life (5730±30 years). Since the 14C is significantly hazardous for human being, the appropriate process to treat 14C is necessary. From the nuclear power plant, the ion exchange resin, graphite, and activated carbon are the main source of 14C. During the effort to reduce the volume of those wastes, the 14C is inevitably occurred as carbon dioxide (CO2) form, so called 14CO2. Thus, the development of technology to permanently capture and safely dispose 14CO2 is required. In this presentation, we introduce the decommissioning technology ranging from 14CO2 capture to solidification. First, the new class of glass adsorbent is developed which can irreversibly capture CO2 even under mild conditions. This material promotes the dissolution of alkaline earth ions due to the unstable glass structure. Then, the physical and chemical optimization of glass adsorbent enhances the performance of CO2 capture. Further, room temperature geopolymeric solidification is also performed to safely dispose 14C without any potential release.

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.

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.

Radioactive carbon dioxide (14CO2) capture using innovative materials is desirable due to associated radiological hazards, and growing climate change. Mineral carbonation technology (MCT) is amenable to irreversibly capture CO2. Typically, MCT is attractive because capturing carbon through the chemical reaction between alkaline earth metal ions and CO2 forms insoluble and significantly stable carbonates. However, most applications of MCT have an intrinsic restriction regarding their operational conditions since no forward reaction occurs within realistic time scales. Thereby, the CO2 capture performance, such as CO2 capacity and carbonation reaction rate, of MCTs and their applications are severely restricted by the difficulty of operations under mild conditions. For example, natural minerals require aggressive carbonation reaction conditions e.g. high pressure (≥ 20 bar), high temperature (> 373 K), and pH-adjusted carrier solutions. To overcome such obstacles, the fabrication of alkaline earth oxides impregnated into an amorphous glass structure have been recently developed. They show enhanced rates of dissolution of alkaline earth metal ions and carbonation reaction due to the loosely packed glass structure and the generation of a surface coating silica gel, consequently facilitating CO2 capture under mild conditions. In this presentation, we report the synthesis and application of a crystallized glass tailored by controlled heat treatment for CO2 capture under mild conditions. The controlled heat treatment of an alkaline earth oxide-containing glass gives rise to a structural transformation from amorphous to crystalline. The structural characterizations and CO2 capture performance, including CO2 capacity, carbonation reaction rate, and the dissolution rate of alkaline earth metal ion, were analyzed to reveal the impact of controlled heat treatment and phase transformation.

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.

Nuclear weapon generates huge amount of radioactive fallout which is extremely dangerous. The fallout gradually falls to the ground and then covers every surface in city and nature. A hydrogel decontamination medium has been developed to clean the surface polluted by the fallout. The hydrogel is soluble in water so the used hydrogel can be simply removed from the surface by washing. However, significant amount of waste water, containing the radioactive fallout, is generated with this process. In this respect, it is necessary to secure alternative technical options for the used hydrogel recovery. In this study, a steam-suction process was suggested for the used hydrogel recovery. Contaminated stainless steel surface, with fixed simulated fallout particles, was prepared for test. The simulated fallout particles were obtained by high-temperature treatment of a mixture of natural soil, used concrete, and Fe2O3. The hydrogel, composed of poly-vinyl alcohol and borax, was spread onto the contaminated stainless steel surface. The hydrogel was soft at first and it gradually becomes rigid with time. The used hydrogel was recovered by suction with a simultaneous steam spraying to soften the rigid gel. As a result, the clean surface of the stainless steel without the simulated fallout particles was obtained, showing the feasibility of this technique for the used hydrogel recovery.

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.