In the present work, we address the new route for the green synthesis of manganese dioxide (MnO2) by an innovative method named the solution plasma process (SPP). The reaction mechanism of both colloidal and nanostructured MnO2 was investigated. Firstly, colloidal MnO2 was synthesized by plasma discharging in KMnO4 aqueous solution without any additives such as reducing agents, acids, or base chemicals. As a function of the discharge time, the purple color solution of MnO4 - (oxidation state +7) was changed to the brown color of MnO2 (oxidation state +4) and then light yellow of Mn2+ (oxidation state +2). Based on the UV-vis analysis we found the optimal discharging time for the synthesis of stable colloidal MnO2 and also reaction mechanism was verified by optical emission spectroscopy (OES) analysis. Secondly, MnO2 nanoparticles were synthesized by SPP with a small amount of reducing sugar. The precipitation of brown color was observed after 8 min of plasma discharge and then completely separated into colorless solution and precipitation. It was confirmed layered type of nanoporous birnessite- MnO2 by X-ray powder diffraction (XRD), fourier-transform infrared spectroscopy (FT-IR), and electron microscopes. The most important merits of this approach are environmentally friendly process within a short time compared to the conventional method. Moreover, the morphology and the microstructure could be controllable by discharge conditions for the appropriate potential applications, such as secondary batteries, supercapacitors, adsorbents, and catalysts.

In this study, we have fabricated the phenolic resin (PR)/polyacrylonitrile (PAN) blend-derived core-sheath nanostructured carbon nanofibers (CNFs) via one-pot solution electrospinning. The obtained core-sheath nanostructured carbon nanofibers were further treated by mixed salt activation process to develop the activated porous CNFs (CNF-A). Compared to pure PAN-based CNFs, the activated PR/PAN blend with PR 20% (CNF28-A)-derived core-sheath nanostructured CNFs showed enhanced specific capacitance of ~ 223 F g− 1 under a three-electrode configuration. Besides, the assembled symmetric CNF28-A//CNF28-A device possessed a specific capacitance of 76.7 F g− 1 at a current density of 1 A g− 1 and exhibited good stability of 111% after 5,000 galvanostatic charge/discharge (GCD) cycles, which verifies the outstanding long-term cycle stability of the device. Moreover, the fabricated supercapacitor device delivered an energy density of 8.63 Wh kg− 1 at a power density of 450 W kg− 1.

고용량 배터리에 대한 요구가 증가에 따라 기존 음극재보다 높은 용량(3,860 mAh/g)과 낮은 전기화학적 전위(– 3.040 V)를 갖는 리튬 금속 기반 음극재에 대한 연구가 활발하게 이루어지고 있다. 본 연구에서는 수열 합성을 통해 제작된 아나타제(anatase) 타입의 TiO2 나노 입자 기반한 PVdF-HFP/TiO2 복합체를 리튬 금속 음극의 계면 보호층으로 적용하였다. 결정구조 및 형상 분석을 통해 유/무기-리튬 나노복합체 박막의 형성을 확인하였다. 또한, 전지화학 테스트(사이클 테스트 및 전압 프로파일)를 통해 리튬 금속 음극의 전기화학 성능은 복합체 보호막이 TiO2 10 wt%, 코팅 두께 1.1 μm의 조건에서 가장 개선된 전기화학적 성능(콜롱 효율 유지: 77 사이클 동안 90% 이상) 발현을 확인하였다. 이를 통해, 처리하지 않은 리튬 전극 대비 본 보호층에 의한 리튬 금속 음극의 성능 안정화/개선 효과가 검증되었다.

Engineering the microstructure of the carbonaceous materials is a promising strategy to enhance the capacitive performance of supercapacitors. In this work, nanostructured Black Pearl (1500 BP) carbon which is a conductive carbon being commercially used in printing rolls, conductive packaging, conductive paints, etc. is analyzed for its feasibility as an electrode material for Electric Double-Layer Capacitors (EDLCs). To achieve that commercial Black Pearl (BP), carbon is treated with mild acid H3PO4 to remove the impurities and enhance the active sites by regulating the growth of agglomerates and creating micropores in the nano-pigments. Generally, the coalescence of nanoparticles owing to their intrinsic surface energy has tendency to create voids of different sizes that act like meso/micropores facilitating the diffusion of ions. The electrochemical performance of BP carbon before and after chemical activation is investigated in aqueous ( H2SO4, KOH and KCl) and a non-aqueous electrolyte (1 M TEMABF4 in acetonitrile) environment employing different electrochemical techniques such as Cyclic Voltammetry (CV), Galvanostatic charge/discharge (GCD) and Electrochemical Impendence Spectroscopy (EIS). The chemically activated BP carbon delivers the highest specific capacitance of ∼156 F g−1 in an aqueous electrolyte, 6 M KOH. The highest specific power, ~ 15.3 kW kg−1 and specific energy, 14.6 Wh kg−1 are obtained with a symmetric capacitor employing non-aqueous electrolyte because of its high working potential, 2.5 V.

Synthesizing nanostructured thin films of oxide semiconductors is a promising approach to fabricate highly efficient photoelectrodes for hydrogen production via photoelectrochemical (PEC) water splitting. In this work, we investigate the feasibility as an efficient photoanode for PEC water oxidation of zinc oxide (ZnO) nanostructured thin films synthesized via a simple method combined with sputtering Zn metallic films on a fluorine-doped tin oxide (FTO) coated glass substrate and subsequent thermal oxidation of the sputtered Zn metallic films in dry air. Characterization of the structural, optical, and PEC properties of the ZnO nanostructured thin film synthesized at varying Zn sputtering powers reveals that we can obtain an optimum ZnO nanostructured thin film as PEC photoanode at a sputtering power of 40 W. The photocurrent density and optimal photocurrent conversion efficiency for the optimum ZnO nanostructured thin film photoanode are found to be 0.1 mA/cm2 and 0.51 %, respectively, at a potential of 0.72 V vs. RHE. Our results illustrate that the ZnO nanostructured thin film has promising potential as an efficient photoanode for PEC water splitting.

This study deals with the effects of austempering time on the microstructure and mechanical properties of ultrahigh strength nanostructured bainitic steels with high carbon and silicon contents. The steels are composed of bainite, martensite and retained austenite by austempering and quenching. As the duration of austempering increases, the thickness of bainitic ferrite increases, but the thickness of retained austenite decreases. Some retained austenites with lower stability are more easily transformed to martensite during tensile testing, which has a detrimental effect on the elongation due to the brittleness of transformed martensite. With increasing austempering time, the hardness decreased and then remained stable because the transformation to nanostructured bainite compensates for the decrease in the volume fraction of martensite. Charpy impact test results indicated that increasing austempering time improved the impact toughness because the formation of brittle martensite was prevented by the decreased fraction and increased stability of retained austenite.

Recently, the properties of nanostructured materials as advanced engineering materials have received great attention. These properties include fracture toughness and a high degree of hardness. To hinder grain growth during sintering, it is necessary to fabricate nanostructured materials. In this respect, a high-frequency induction-heated sintering method has been presented as an effective technique for making nanostructured materials at a lower temperature in a very short heating period. Nanopowders of W and Al2O3 are synthesized from WO3 and Al powders during high-energy ball milling. Highly dense nanostructured W-Al2O3 composites are made within three minutes by high-frequency induction-heated sintering method and materials are evaluated in terms of hardness, fracture toughness, and microstructure. The hardness and fracture toughness of the composite are 1364 kg/mm2 and 7.1 MPa·m1/2, respectively. Fracture toughness of nanostructured W-Al2O3 is higher than that of monolithic Al2O3. The hardness of this composite is higher than that of monolithic W.

Nanostructured lipid carriers (NLC) are getting attention as delivery system for nutraceuticals due to its low toxicity and higher loading efficiency of active ingredients. However, the cytotoxicity of NLC had not fully evaluated especially on neuroblastoma. In this study, cytotoxicity of NLC and curcumin-loaded NLC (C-NLC) were evaluated on SH-SY5Y neuroblastoma cells investigating cell morphology, mitochondrial activity, and reactive oxygen species (ROS) production compared to H2O2 treatment as a positive control. As a result, the metabolic activity was inhibited about 40% by 250ppm of NLC along with morphological change. C-NLC exhibited 50% inhibitory effect on mitochondrial activity at 500ppm, which was lower than NLC itself. Moreover, NLCs significantly induced ROS production which was recognized as one of the indicators of cytotoxicity generated by NLCs. In conclusion, lower cytotoxic effect was observed with NLC on SH-SY5Y neuroblastoma based on ROS production and these investigation could be used for further application of NLC in food industry.

Dyes are widely used in various industries including textile, cosmetic, paper, plastics, rubber, and coating, and their discharge into waterways causes serious environmental and health problems. Four different carbon nanostructures, graphene oxide, oxidized multi-walled carbon nanotubes, activated carbon and multi-walled carbon nanotubes, were used as adsorbents for the removal of Nile Blue A (NBA) dye from aqueous solution. The four carbon nanostructures were characterized by scanning electron microscope and X-ray diffractometer. The effects of various parameters were investigated. Kinetic adsorption data were analyzed using the first-order model and the pseudo-second-order model. The regression results showed that the adsorption kinetics were more accurately represented by the pseudo-second-order model. The equilibrium data for the aqueous solutions were fitted to Langmuir and Freundlich isotherms, and the equilibrium adsorption of NBA was best described by the Langmuir isotherm model. This is the first research on the removal of dye using four carbon nanostructures adsorbents.

The purpose of this study is to evaluate the stability of Epigallocatechin gallate (EGCG) - loaded nanostructured lipid carrier (NLC) after Autoclave sterilization. EGCG, glycerolmonostearate (GMS), oleic acid, and lecithin were mixed as solid lipid phase and subsequently it was heated up to 70°C. Thereafter, the solid lipid phase was mixed with the water phase consisting of Tween 80 and deionized water. Then, ultra-sonication(work time, 5 min; pulse on, 4s; pulse off, 2s), high pressure homogenization(600 bar and 3 cycles) process were proceeded to homogenize NLC particles. The particle size and zeta-potential of NLCs was approximate 100 ~ 120nm and -50 ~ -60mV, respectively. In order to investigate the effect of sterilization on the stability of NLCs, Autoclavesterilization was applied to the NLCs suspension at 121°C for 15 min. After the sterilization, the particle size and zeta potentialtended to be maintained or improved. Moreover, after sterilization, crystal shape was formed and it was considered as transformation of the lipid in NLCs (from α to β) because of recrystallization upon heating. In conclusion, sterilization process can be helpful to improve the stability of NLCs.

이 연구에서는 nanostructured lipid carrier (NLC)를 음료에 적용했을 경우, 음료 살균 시안정성 및 품질을 평가하고 자 하였다. Glycerol monostearate (GMS), oleic acid, lecithin을 포함한 유상을 준비하였고, 증류수에 Tween 80을 분 산시켜 수상을 준비하였다. 준비된 두 상을 80℃까지 가열한 후, 두 가지 상을 섞어 교반하였다. 이후 high shear homogenization (3,000 rpm / 5분)과 ultra-sonication (work time : 4 s / rest time : 2 s)를 처리한 후, high pressure homogenizer (600 bar / 3 cycle)를 이용해 세 차례에 거쳐 균질화를 진행하였다. 제조된 NLC의 특성을 분석한 결과, 약 120-250 nm 크기의 입자가 형성되었고 안정한 상태를 유지하는 것으로 나타났다. NLC의 음료 적용 시 살균 안정성을 평가하기 위하여 물 71.68 ml, sucrose 8 g, citric acid 0.15 g, ascorbic acid 0.1 g, orange flavor 0.07 g를 배합하여 NLC 20ml화 혼합하였다. 제조된 음료를 62℃-65℃에서 30분간 가열살균(low temperature long time, LTLT)하였다. 살균한 직후 NLC의 안정성을 평가한 결과, NLC의 크기가 다소 증가하였으나 그 차이는 미미하여 NLC가 음료 내에 안정적 으로 존재함을 확인하였다. 결론적으로 NLC를 음료에 적용했을 때, 탑재되는 물질의 건강 증진 효과가 잘 유지될 수 있을 것으로 기대된다.

TiH2 nanopowder was made by high energy ball milling. The milled TiH2 and CNT powders were then simultaneously synthesized and consolidated using pulsed current activated sintering (PCAS) within one minute under an applied pressure of 80 MPa. The milling did not induce any reaction between the constituent powders. Meanwhile, PCAS of the TiH2-CNT mixture produced a Ti-TiC composite according to the reaction (0.92TiH2 + 0.08CNT→0.84Ti + 0.08TiC + 0.92H2, 0.84TiH2 + 0.16CNT→0.68Ti + 0.16TiC + 0.84H2). Highly dense nanocrystalline Ti-TiC composites with a relative density of up to 99.7% were obtained. The hardness and fracture toughness of the dense Ti-8 mole% TiC and Ti-16 mole% TiC produced by PCAS were also investigated. The hardness of the Ti-8 mole% TiC and Ti-16 mole% TiC composites was higher than that of Ti. The hardness value of the Ti-16 mole% TiC composite was higher than that of the Ti-8 mole% TiC composite without a decrease in fracture toughness.

Despite having many attractive properties, ZrO2 ceramic has a low fracture toughness which limits its wide application. One of the most obvious tactics to improve its mechanical properties has been to add a reinforcing agent to formulate a nanostructured composite material. Nanopowders of ZrO2 and Cr were synthesized from CrO3 and Zr powder by high energy ball milling for 10 h. Dense nanocrystalline 2/3Cr-ZrO2 composite was consolidated by a high-frequency induction heated sintering method within 5 min at 600˚C from mechanically synthesized powder. The method was found to enable not only rapid densification but also the inhibition of grain growth, preserving the nano-scale microstructure. Highly dense 2/3Cr-ZrO2 composite with relative density of up to 99.5% was produced under simultaneous application of a 1 GPa pressure and the induced current. The hardness and fracture toughness of the composite were 534 kg/mm2 and 7MPa·m1/2, respectively. The composite was determined to have good biocompatibility.

The current concern about these materials (MoSi2 and NbSi2) focuses on their low fracture toughness below theductile-brittle transition temperature. To improve the mechanical properties of these materials, the fabrication of nanostructuredand composite materials has been found to be effective. Nanomaterials frequently possess high strength, high hardness, excellentductility and toughness, and more attention is being paid to their potential application. In this study, nanopowders of Mo, Nb,and Si were fabricated by high-energy ball milling. A dense nanostructured MoSi2-NbSi2 composite was simultaneouslysynthesized and sintered within two minutes by high-frequency induction heating method using mechanically activated powdersof Mo, Nb, and Si. The high-density MoSi2-NbSi2 composite was produced under simultaneous application of 80MPa pressureand an induced current. The sintering behavior, mechanical properties, and microstructure of the composite were investigated.The average hardness and fracture toughness values obtained were 1180kg/mm2 and 3MPa·m1/2, respectively. These fracturetoughness and hardness values of the nanostructured MoSi2-NbSi2 composite are higher than those of monolithic MoSi2 orNbSi2.

We report the effect of the fabric of the surface microstructure on the CO gas sensing properties of SnO2 thin films deposited on self-assembled Au nanodots (SnO2/Au) that were formed on SiO2/Si substrates. We characterized structural and morphological properties, comparing them to those of SnO2 thin films deposited directly onto SiO2/Si substrates. We observed a significant enhancement of CO gas sensing properties in the SnO2/Au gas sensors, specifically exhibiting a high maximum response at 200˚C and quite a low detection limit of 1 ppm level in dry air. In particular, the response of the SnO2/Au gas sensor was found to reach the maximum value of 32.5 at 200˚C, which is roughly 27 times higher than the response (~1.2) of the SnO2 gas sensor obtained at the same operating temperature of 200˚C. Furthermore, the SnO2/Au gas sensors displayed very fast response and recovery behaviors. The observed enhancement in the CO gas sensing properties of the SnO2/Au sensors is mainly ascribed to the formation of a nanostructured morphology in the active SnO2 layer having a high specific surface-reaction area by the insertion of a nanodot form of Au nucleation layer.

Nanocrystalline materials have received much attention as advanced engineering materials with improved physical and mechanical properties, including high strength, high hardness, excellent ductility and toughness. In this study, nanopowders of Al2O3, MgO and TiO2 were prepared as starting materials by high energy ball milling for the simultaneous synthesis and sintering of the nanostructured compound Mg4Al2Ti9O25 by high-frequency induction heating process. The highly dense nanostructured Mg4Al2Ti9O25 compound was produced within one minute by the simultaneous application of 80MPa pressure and induced current. The sintering behavior, grain size and mechanical properties of the Mg4Al2Ti9O25 compound were evaluated.

Nanocrystalline materials have recently received significant attention in the area of advanced materials engineering due to their improved physical and mechanical properties. A solid-solution nanocrystalline powder, (Ti,Mo)C, was prepared via high-energy milling of Ti-Mo alloys with graphite. Using XRD data, the synthesis process was investigated in terms of the phase evolution. Rapid sintering of nanostuctured (Ti,Mo)C hard materials was performed using a pulsed current activated sintering process (PCAS). This process allows quick densification to near theoretical density and inhibits grain growth. A dense, nanostructured (Ti,Mo)C hard material with a relative density of up to 96 % was produced by simultaneous application of 80 MPa and a pulsed current for 2 min. The average grain size of the (Ti,Mo)C was lower than 150 nm. The hardness and fracture toughness of the dense (Ti,Mo)C produced by PCAS were also evaluated. The fracture toughness of the (Ti,Mo)C was higher than that of TiC.

We investigated the carbon monoxide (CO) gas-sensing properties of nanostructured Al-doped zinc oxide thin films deposited on self-assembled Au nanodots (ZnO/Au thin films). The Al-doped ZnO thin film was deposited onto the structure by rf sputtering, resulting in a gas-sensing element comprising a ZnO-based active layer with an embedded Pt/Ti electrode covered by the self-assembled Au nanodots. Prior to the growth of the active ZnO layer, the Au nanodots were formed via annealing a thin Au layer with a thickness of 2 nm at a moderate temperature of 500˚C. It was found that the ZnO/Au nanostructured thin film gas sensors showed a high maximum sensitivity to CO gas at 250˚C and a low CO detection limit of 5 ppm in dry air. Furthermore, the ZnO/Au thin film CO gas sensors exhibited fast response and recovery behaviors. The observed excellent CO gas-sensing properties of the nanostructured ZnO/Au thin films can be ascribed to the Au nanodots, acting as both a nucleation layer for the formation of the ZnO nanostructure and a catalyst in the CO surface reaction. These results suggest that the ZnO thin films deposited on self-assembled Au nanodots are promising for practical high-performance CO gas sensors.

Nanostructured was synthesized to have high density via rapid and cost effective process named as high-frequency induction heated combustion synthesis(HFIHCS) method. For the process, mechanically activated Re-Si powder was used, which had been prepared by mechanical ball milling of Re and Si powders with mixing ratio of 1:1.75. Both combustion synthesis and densification were accomplished simultaneously by applying electric current and mechanical pressure of 80 MPa during the process. The average grain size, hardness, and fracture toughness of the compound were 210 nm, 1085 and 4 , respectively. The experimental results show that HFIHCS is a promising process for synthesis of nanostructured which has a potential for both high temperature and thermo-electric applications