Cutting reactor pressure vessels (RPV) into acceptable sizes for waste disposal is a key process in dismantling nuclear power plants. In the case of Kori-1, a remote oxyfuel cutting method has been developed by Doosan Heavy Industry & Construction to dismantle RPVs. Cutting radioactive material, such as RPV, generates a large number of fine and ultrafine particles incorporating radioactive isotopes. To minimize radiological exposure of dismantling workers and workplace surface contamination, understanding the characteristics of radioactive aerosols from the cutting process is crucial. However, there is a paucity of knowledge of the by-products of the cutting process. To overcome the limitations, a mock-up RPV cutting experiment was designed and established to investigate the characteristics of fine and ultrafine particles from the remote cutting process of the RPV at the Nuclear Decommissioning Center of Doosan Heavy Industry & Construction. The aerosol measurement system was composed of a cutting system, purification system, sampling system, and measurement device. The cutting system has a shielding tent and oxyfuel cutting torch and remote cutting robot arm. It was designed to prevent fine particle leakage. The shielding tent acts as a cutting chamber and is connected to the purification system. The purification system operates a pressure difference by generating an airflow which delivers aerosols from the cutting system to the purification system. The sampling system was installed at the center of the pipe which connects the shielding tent and purification system and was carefully designed to achieve isokinetic sampling for unbiased sampling. Sampled aerosols were delivered to the measurement device. A high-resolution electrical low-pressure impactor (HR-ELPI+, Dekati) is used to measure the size distribution of inhalable aerosols (Aerodynamic diameter: 6 nm to 10 μm) and to collect size classified aerosols. In this work, the mock-up reactor vessel was cut 3 times to measure the number distribution of fine and ultrafine particles and mass distribution of iron, chromium, nickel, and manganese. The number distribution of aerosols showed the bi-modal distribution; two peaks were positioned at 0.01−0.02 μm and 0.04–0.07 μm respectively. The mass distribution of metal elements showed bi-modal and trimodal distribution. Such results could be criteria for filter selection to be used in the filtration system for the cutting process and fundamental data for internal dose assessment for accidents. Future work includes the investigations relationships between the characteristics of the generated aerosols and physicochemical properties of metal elements.

Smart materials capable of changing their characteristics in response to stimuli such as light, heat, pH, and electric and magnetic fields are promising for application to flexible electronics, soft robotics, and biomedicine. Compared with conventional rigid materials, these materials are typically composed of soft materials that improve the biocompatibility and allow for large and dynamic deformations in response to external environmental stimuli. Among them, smart magnetic materials are attracting immense attention owing to their fast response, remote actuation, and wide penetration range under various conditions. In this review, we report the material design and fabrication of smart magnetic materials. Furthermore, we focus on recent advances in their typical applications, namely, soft magnetic actuators, sensors for self-assembly, object manipulation, shape transformation, multimodal robot actuation, and tactile sensing.

Composite materials offer distinct and unique properties that are not naturally inherited in the individual materials that make them. One of the most attractive composites to manufacture is the aluminum alloy matrix composite, because it usually combines easiness of availability, light weight, strength, and other favorable properties. In the current work, Powder Metallurgy Method (PMM) is used to prepare Al2024 matrix composites reinforced with different mixing ratios of yttrium oxide (Y2O3) particles. The tests performed on the composites include physical, mechanical, and tribological, as well as microstructure analysis via optical microscope. The results show that the experimental density slightly decreases while the porosity increases when the reinforcement ratio increases within the selected range of 0 ~ 20 wt%. Besides this, the yield strength, tensile strength, and Vickers hardness increase up to a 10 wt% Y2O3 ratio, after which they decline. Moreover, the wear results show that the composite follows the same paradigm for strength and hardness. It is concluded that this composite is ideal for application when higher strength is required from aluminum composites, as well as lighter weight up to certain values of Y2O3 ratio.

The purpose of this study is to optimize the powder formulation and manufacturing conditions for the solidification of an extract of the herb Bangpungtongseong-san (BPTS). To develop BPTS-loaded particles for the tablet dosage form, various BPTS-loaded particles composed of BPTS, dextrin, microcrystalline cellulose (MCC), silicon dioxide, ethanol, and water are prepared using spray-drying and high shear granulation (high-speed mixing). Their physical properties are evaluated using scanning electron microscopy and measurements of the angle of repose, Hausner ratio, Carr’s index, hardness, and disintegration time. The optimal BPTS-loaded particles exhibit improved flowability and compressibility. In particular, the BPTS-loaded particles containing silicon dioxide show significantly improved flowability and compressibility (the angle of repose, Hausner ratio, and Carr’s index are 35.27 ± 0.58°, 1.18 ± 0.06, and 15.67 ± 1.68%, respectively), hardness (18.97 ± 1.00 KP), and disintegration time (17.60 ± 1.50 min) compared to those without silicon dioxide. Therefore, this study suggests that particles prepared by high-speed mixing can be used to greatly improve the flowability and compressibility of BPTS using MCC and silicon dioxide.

가교된 단분산 폴리스티렌 비드를 유화 중합과 분산 중합으로 합성하였다. 가교된 폴리스티렌 비드를 자일렌과 iron pentacarbonyl로 팽윤시킨 후 옥틸 에테르와 함께 환류하여 iron pentacarbonyl을 산화철로 변환시켰다. 산화철의 화학 안정성을 향상시키기 위해 산화철을 포함하는 폴리스티렌 비드를 실리카로 코팅하였다. 소결로 폴리스티렌 비드를 제거하여 산화철을 포함하는 중공 실리카 비드를 얻었다. 전체 합성 과정에서 모든 비드의 크기와 형태는 균일하게 유지되었고, 산화철을 포함하는 중공 실리카 입자는 강한 자성을 보였다.

Zinc selenide (ZnSe) nanoparticles were synthesized in aqueous solution using glutathione (GSH) as a ligand. The influence of the ligand content, reaction temperature, and hydroxyl ion concentration (pH) on the fabrication of the ZnSe particles was investigated. The optical properties of the synthesized ZnSe particles were characterized using various analytical techniques. The nanoparticles absorbed UV-vis light in the range of 350-400 nm, which is shorter than the absorption wavelength of bulk ZnSe particles (460 nm). The lowest ligand concentration for achieving good light absorption and emission properties was 0.6 mmol. The reaction temperature had an impact on the emission properties; photoluminescence spectroscopic analysis showed that the photo-discharge characteristics were greatly enhanced at high temperatures. These discharge characteristics were also affected by the hydroxyl ion concentration in solution; at pH 13, sound emission characteristics were observed, even at a low temperature of 25oC. The manufactured nanoparticles showed excellent light absorption and emission properties, suggesting the possibility of fabricating ZnSe QDs in aqueous solutions at low temperatures.

Molybdenum trioxide (MoO3) is used in various applications including sensors, photocatalysts, and batteries owing to its excellent ionic conductivity and thermal properties. It can also be used as a precursor in the hydrogen reduction process to obtain molybdenum metals. Control of the parameters governing the MoO3 synthesis process is extremely important because the size and shape of MoO3 in the reduction process affect the shape, size, and crystallization of Mo metal. In this study, we fabricated MoO3 nanoparticles using a solution combustion synthesis (SCS) method that utilizes an organic additive, thereby controlling their morphology. The nucleation behavior and particle morphology were confirmed using ultraviolet-visible spectroscopy (UV-vis) and field emission scanning electron microscopy (FE-SEM). The concentration of the precursor (ammonium heptamolybdate tetrahydrate) was adjusted to be 0.1, 0.2, and 0.4 M. Depending on this concentration, different nucleation rates were obtained, thereby resulting in different particle morphologies.

In this study, epoxy composites were reinforced with multi-walled carbon nanotubes and fused silica particles, dispersing the fillers within the epoxy resin based on a simple physical method using only shear mixing and ultrasonication. The hybrid composite specimens with 0.6 wt% of carbon nanotubes and 50 wt% of silica particles showed improved mechanical properties, with increase in tensile strength and Young’s modulus up to 12 and 37%, respectively, with respect to those of the baseline specimens. The experimental results showed that the low thermal expansion of the silica particles improved the thermal stability of the composites compared with that of the baseline specimen, whereas the thermal expansion slightly increased, due to the increased heat transfer from the exterior to the interior of specimens by the carbon nanotube filler. The coefficient of thermal expansion of the hybrid composite specimen reinforced with 0.6 wt% of carbon nanotubes and 50 wt% of silica particles was decreased by 25%, and the thermal conductivity was increased by about 84%, compared with those of the baseline specimen.