목적 : 본 연구는 세륨(IV)-지르코늄(IV) 산화물 나노입자를 사용하여 콘택트렌즈를 제조한 후, 안의료용 기능성 렌즈로의 사용 가능을 확인 위해 제조된 렌즈의 물성을 비교 분석하였다. 방법 : 2-Hydroxyethyl methacrylate에 나노 세륨-지르코늄 산화물(cerium(IV)-zirconium(IV) oxide)을 첨가하여 공중합 한 후 물성을 측정하고, 친수성 단량체인 methacrylic acid(MA)를 추가로 첨가하여 물성을 측정, 비교하였다. 결과 : 다양한 비율의 세륨(IV)-지르코늄(IV) 산화물 나노입자와 MA를 첨가한 렌즈의 물성을 평가한 결과, UV-B 투과율은 40.95~66.26%, 굴절률 1.4163~1.4357, 함수율 37.44~47.18%, 접촉각 36.87~56.36°, 인장 강도 0.0612~0.561 kgf/mm², 표면거칠기 7.70~8.72 nm로 각각 측정되었다. 나노입자 및 MA 첨가는 습윤성, 인장강도 및 중합안정성을 향상시키고, UV-B 투과율과 표면거칠기를 감소시켰으며, 황색포도상구균에 대한 항균 성이 확인되었다. 결론 : 세륨(IV)-지르코늄(IV) 산화물 나노입자에 MA를 첨가하여 제조한 렌즈가 중합 안정성, 내구성, 습윤성 을 향상시키는 것을 확인하였으며, 따라서 안의료용 기능성 콘택트렌즈 소재로 활용할 수 있을 것으로 판단된다.

나노에멀젼은 일반적으로 입자 크기가 20~200nm로 특유의 푸른빛을 띠며 투명하거나 반투명한 외관부터 유백색의 외관을 띤다. 입자가 작고 고르므로 장기간 안정할 수 있고, 유효성분의 피부 투과율 증 진에 도움을 줄 수 있어 다방면으로 활용되고 있다. 본 연구에서는 고에너지 유화 방법과 저에너지 유화 방법을 사용하여 나노에멀젼 형성 능력을 비교하였다. Polysorbate 60 (HLB 14.9), PEG-60 hydrogenated castor oil (HLB 14.0)을 계면활성제로써 각각 사용하여 나노에멀젼을 제조하였다. 제조 방 식으로는 직접 유화와 고압 유화, 상반전 유화를 활용하였다. 오일의 종류에 따라 나노에멀젼의 형성 능력 이 달랐으며, 에스터계 오일만이 21.5~105.0 nm 범위의 입자 사이즈를 나타내어 우수한 나노에멀젼 형성 을 보여주었다. 더불어, 제조 방식에 따라 나노에멀젼의 입자 사이즈가 다름을 나타내었다. 특히 Rotor/Stator 교반기를 이용한 직접 유화 방식의 입자 사이즈는 28.0~61.2 ± 1.2~17.5 nm로 비교적 큰 변화를 보이지 않고 안정한 것을 확인할 수 있었다. 저에너지와 고에너지 유화 방법의 입자 사이즈는 각각 24.9~105.0 nm와 24.1~75.3 nm로 얻어졌다. 이는 저에너지 방법으로도 입자가 작은 나노에멀젼을 효과 적으로 형성할 수 있음을 나타내며, 이러한 방법에 대한 에너지 효율을 시사한다. 또한, 본 실험에선 동일한 조성에서 유화 방법보다는 오일의 종류가 나노에멀젼 형성에 좀 더 지배적임을 확인함으로써 나노에멀 젼 제조 시에 필요한 물리적인 에너지 크기보다는 상호작용하는 물질 간의 친화성이 비교적 중요한 것으로 사료된다.

The heat transfer characteristics of double-pipe spiral heat exchanger using aluminum oxide nano-fluid were investigated by three different sizes of curvature size, experimentally. Five concentration of nano-fluid as working fluid were made and tested to analyze the heat transfer characteristics. As results, the heat transfer performance was improved at 0.25% of nano-fluid due to high thermal conductivity, however, as the concentration of nanofluid increased (~2.0%), the heat transfer performance deteriorated due to the increase in thermal resistance caused by the sedimentation of particles in the flow path. In addition, the nano-fluid has a higher pressure drop than water due to its high density and viscosity. The optimal range for heat transfer enhancement of nano-fluid was found to be less than 4.0 LPM in flow rate and 0.25% of nano-fluid concentration in this study.

Mo-ODS alloys have excellent mechanical properties, including an improved recrystallization temperature, greater strength due to dispersed oxides, and the ability to suppress grain growth at high temperatures. In ODS alloys, the dispersed Y2O3 and added Ti form Y-Ti-O complex oxides, producing finer particles than those in the initial Y2O3. The complex oxides increase high-temperature stability and improve the mechanical properties of the alloy. In particular, the use of TiH2 powder, which is more brittle than conventional Ti, can enable the distribution of finer oxides than is possible with conventional Ti powder during milling. Moreover, dehydrogenation leads to a more refined powder size in the reduction process. This study investigated the refinement of Yi2Ti2O7 in a nano Mo-ODS alloy using TiH2. The alloy compositions were determined to be Mo-0.5Ti-0.5Yi2O3 and Mo-1.0Ti-0.5Yi2Oi2. The nano Mo-ODS alloys were fabricated using Ti and TiH2 to explore the effects of adding different forms of Ti. The sintered specimens were analyzed through X-ray diffraction for phase analysis, and the microstructure of the alloys was analyzed using scanning electron microscopy and transmission electron microscopy. Vickers hardness tests were conducted to determine the effect of the form of Ti added on the mechanical properties, and it was found that using TiHi2 effectively improved the mechanical properties.

Activated carbon has broad application prospects for treating pollutants due to its easy availability, low cost and good adsorption. In our work, nano-activated carbons (NAC) with abundant functional groups are obtained by the oxidation modification of HNO3, ( NH4)2S2O8, and KMnO4, which are used to construct the particle electrodes to degrade NDEA in a continuous flow electrochemical reactor, and the influence of relevant factors on the performance of NDEA removal is discussed. The experimental data show that the optimal degradation efficiency is 42.55% at the conditions of 3 mL/min influent water flow, 0.21 M electrolyte concentration, 10 mA/cm2 current density, and 10 μg/mL initial NDEA concentration. The degradation of NDEA conforms to a quasi second order kinetic equation. The electrocatalytic mechanism of NAC electrodes for removing NDEA is firstly discussed. The effects of different free radicals on the degradation of NDEA are also demonstrated through free radical quenching experiments, indicating that the degradation of NDEA is dominated by ⋅OH. The degradation pathway of NDEA and final products are obtained using GC–MS. NAC particle electrodes as the cheap and efficient electrocatalyst in continuous flow electrochemical reactor system provide a greener solution for the removal of disinfection by-products from drinking water.

In this study, we report significant improvements in lithium-ion battery anodes cost and performance, by fabricating nano porous silicon (Si) particles from Si wafer sludge using the metal-assisted chemical etching (MACE) process. To solve the problem of volume expansion of Si during alloying/de-alloying with lithium ions, a layer was formed through nitric acid treatment, and Ag particles were removed at the same time. This layer acts as a core-shell structure that suppresses Si volume expansion. Additionally, the specific surface area of Si increased by controlling the etching time, which corresponds to the volume expansion of Si, showing a synergistic effect with the core-shell. This development not only contributes to the development of high-capacity anode materials, but also highlights the possibility of reducing manufacturing costs by utilizing waste Si wafer sludge. In addition, this method enhances the capacity retention rate of lithium-ion batteries by up to 38 %, marking a significant step forward in performance improvements.

In the current study, the epoxy material was mixed with 10%, and 30% weight percent carbon material as filler in different thicknesses (1 cm, 1.5 cm, and 2 cm). Transmission electron microscope (TEM) measurements showed the average size of the nano-carbon was 20 nm with a standard deviation of 5 nm. The morphology of samples was examined using scanning electron microscopy (SEM), which showed the flatness of the epoxy surface, and when the content of carbon increases, the connection between the epoxy array and carbon increases. The compression test indicates the effect of nano-size on enhancing the mechanical properties of the studied samples. To survey the shielding properties of the epoxy/carbon composites using gamma-rays emitted from Am-241, Ba-133, Cs-137, Co-60, and Eu-152 sources, which covered a wide range of energies from 0.059 up to 1.408 MeV, the gamma intensity was measured using the NaI (Tl) detector. The linear and mass attenuation coefficients were calculated by obtaining the area under each peak of the energy spectrum observed from Genie 2000 software in the presence and absence of the sample. The experimental results obtained were compared theoretically with XCOM software. The comparison examined the validity of experimental results where the relative division rate ranged between 0.02 and 2%. Also, the measurement of the relative division rate between linear attenuation coefficients of microand nano-composites was found to range from 0.9 to 21% The other shielding parameters are calculated at the same range of energy, such as a half-value layer (HVL), mean free path (MFP), tenth-value layer (TVL), effective atomic number (Zeff), and the buildup factors (EBF and EABF). The data revealed a consistent reduction in the particle size of the shielding material across various weight percentages, resulting in enhanced radiation shielding capabilities. The sample that contains 30% nano-carbon has the lowest values of TVL (29.4 cm) and HVL (8.85 cm); moreover, it has the highest value of the linear attenuation coefficient (LAC), which makes it the best in its ability to attenuate radiation.

Mg81Ni19-8wt.% REO (oxides of Lanthanum and Cerium) alloys were successfully prepared using mechanical alloying method with Mg-Ni alloy and REO powder. Phase analysis, structural characterization, and microstructure imagine of the alloys were conducted using X-ray diffraction (XRD), metallurgical microscope, and transmission electron microscopy (TEM) methods. Multi-phase structures, including the primary phase of Mg2Ni and several secondary phases of Mg + Mg2Ni, MgNi-LaO, and MgNi-CeO, were found in in the as-cast Mg81Ni19- 8wt.% REO alloys. XRD and TEM results showed that Ce exhibits variable valence behavior at various stages, and the addition of REO promotes the nanocrystalline of the alloy. The hydrogen absorption capacity of ball-milled Mg81Ni19 and Mg81Ni19- 8wt.%REO alloy for 2 h at 343 K is 1.34 wt.% and 1.83 wt.%, which are much larger than 0.94 wt.% of as-cast Mg81Ni19 alloy. The addition of REO led to a decrease of the thermal decomposition temperature of the alloy hydride by approximately 20 K and a reduction of the activation energy of the hydrogen desorption reaction by 10% and 13%, respectively.

In this research, synergetic and separate influence of nano-carbon black (C.Bn) and SiC on the microstructure and flexural strength of ZrB2 were investigated. So, ZrB2 and ZrB2- 30vol%-based composites containing 10 and 15 vol% C.Bn as well as ZrB2- 15 vol% SiC were fabricated via spark plasma sintering at 1850 °C for soaking time of 8 min under the applied pressure of 35 MPa. Relative density was measured by Archimedes method. Microstructural evaluation was carried out by applying the field emission electron microscopy (FESEM), and flexural strength was measured by three-point bending test. It was found the relative density improves in the presence of C.Bn and SiC especially in synergetic state so that the full densification was gained in Z30Si10C.Bn and Z30Si15C.Bn composites through their reactions with impurities at 1850 °C. In the monolithic ZrB2 system, the C.Bn addition improves the flexural strength slightly to 300 MPa and 315 MPa from 290 MPa. However, co-doped 10 vol% C.Bn with 30 vol% SiC resulted to achieve maximum flexural strength of 486 MPa in comparison with individually applying each of them (395 MPa for Z30Si and 300 MPa for Z10 C.Bn).

상변화 물질(PCM)은 상전이 동안 에너지를 흡수하거나 방출할 수 있는 잠열 저장 물질로 활용된다. 최근 수십 년 동 안, 연구자들은 다양한 온도 적용을 위한 건설 물질로의 다양한 PCM의 통합을 탐구해 왔다. 그러나, PCM을 통합하는 콘크리트 의 기계적 및 열적 반응은 통합 방법에 의해 영향을 받는다. PCM을 콘크리트에 추가하기 위한 여러 기술이 제안되었다. 그럼 에도 불구하고, 콘크리트에 마이크로 캡슐화 PCM(m-PCM)의 통합은 종종 기계적 강도의 상당한 감소를 초래한다. 기존 콘크리 트에 m-PCM의 추가와 관련된 한계를 극복하기 위해, 예외적인 강도 및 내구성 특성으로 인해 초고성능 시멘트 복합체(UHPCC) 가 선호된다. 따라서, 본 연구에서는 기존 기술의 단점을 해결하기 위해 PCM을 통합한 신규 나노 엔지니어링 UHPCC를 개발하 였다. 또한, 시멘트 복합체의 기계적 및 열적 성능을 향상시키기 위해 다중 벽 탄소 나노튜브(MWCNT)를 추가하였다. 결과는 MWCNT의 포함이 기계적 성능을 향상시켰을 뿐만 아니라 시멘트 복합체의 열적 성능을 향상시켰다는 것을 보여 주었다.

The incorporation of vertically aligned carbon nanotubes (VACNTs) between composites plies has been said to enhance the through-thickness strength, and it can also decrease the risk of interply delamination and reduce crack initiation. Thanks to these high mechanical performances, nano-engineered hybrid composites are seen as promising for highly demanding structural reinforcement applications. This paper is part of a study that focuses specifically on the methodology for transferring VACNTs onto a prepreg surface while maintaining their initial vertically aligned morphology. The chosen method involved bonding the VACNTs’ forest through capillary impregnation of the forest by the prepreg’s resin. Key parameters for an effective transfer and to achieve a partial capillary rise of the resin into the VACNTs will be discussed here.

To develop a high capacity lithium secondary battery, a new approach to anode material synthesis is required, capable of producing an anode that exceeds the energy density limit of a carbon-based anode. This research synthesized carbon nano silicon composites as an anode material for a secondary battery using the RF thermal plasma method, which is an ecofriendly dry synthesis method. Prior to material synthesis, a silicon raw material was mixed at 10, 20, 30, 40, and 50 wt% based on the carbon raw material in a powder form, and the temperature change inside the reaction field depending on the applied plasma power was calculated. Information about the materials in the synthesized carbon nano silicon composites were confirmed through XRD analysis, showing carbon (86.7~52.6 %), silicon (7.2~36.2 %), and silicon carbide (6.1~11.2 %). Through FE-SEM analysis, it was confirmed that the silicon bonded to carbon was distributed at sizes of 100 nm or less. The bonding shape of the silicon nano particles bonded to carbon was observed through TEM analysis. The initial electrochemical charging/ discharging test for the 40 wt% silicon mixture showed excellent electrical characteristics of 1,517 mAh/g (91.9 %) and an irreversible capacity of 133 mAh/g (8.1 %).

In today’s world, carbon-based materials research is much wider wherein, it requires a lot of processing techniques to manufacture or synthesize. Moreover, the processing methods through which the carbon-based materials are derived from synthetic sources are of high cost. Processing of such hierarchical porous carbon materials (PCMs) was slightly complex and only very few methods render carbon nano-materials (CNMs) with high specific surface area. Once it is processed, which paves a path to versatile applications. CNMs derived from biological sources are widespread and their application spectrum is also very wide. This review focuses on biomass-derived CNMs from various plant sources for its versatile applications. The major thrust areas of energy storage include batteries, super-capacitors, and fuel cells which are described in this article. Meanwhile, the challenges faced during the processing of biomass-derived CNMs and their future prospects are also discussed comprehensively.