Porous Cu with a dispersion of nanoscale Al2O3 particles is fabricated by freeze-drying CuO-Al2O3/camphene slurry and sintering. Camphene slurries with CuO-Al2O3 contents of 5 and 10 vol% are unidirectionally frozen at -30oC, and pores are generated in the frozen specimens by camphene sublimation during air drying. The green bodies are sintered for 1 h at 700oC and 800oC in H2 atmosphere. The sintered samples show large pores of 100 μm in average size aligned parallel to the camphene growth direction. The internal walls of the large pores feature relatively small pores of ~10 μm in size. The size of the large pores decreases with increasing CuO-Al2O3 content by the changing degree of powder rearrangement in the slurry. The size of the small pores decreases with increasing sintering temperature. Microstructural analysis reveals that 100-nm Al2O3 particles are homogeneously dispersed in the Cu matrix. These results suggest that a porous composite body with aligned large pores could be fabricated by a freeze-drying and H2 reducing process.

PURPOSES: This study develops eco-friendly asphalt reinforcement materials applicable to bridge deck pavement. The main purpose is to ensure highly reliable quality applicable to structures and the possibility of practical application. The main target of the study is to develop materials that are environmentally friendly and capable of improving performanceMETHODS: The application of double-reinforcement fiber improves the performance of the road pavement. 1. We use recycled film for application of sheet-typed reinforcement. 2. We use preprocessing fibers to reinforce the properties of composite pavement materials.RESULTS : The developed products may produce materials that fit the purpose of achieving stability and environmental friendliness. Sheettyped reinforcements use more than 50% recycled resin. The most important type of damage to the asphalt layer is deflection (plastic deformation). These products have a very high deflection resistance of not less than 6,000 cycles/mm. In addition, all performance is excellent. Thus, it will be easier to access the field in the future.CONCLUSIONS: Fiber-reinforced asphalt pavement showed excellent performance. Sheet-typed reinforcements containing 50% recycling resin produced good performance in terms of functionality as well as environmental friendliness. Thus, enhancing the field applicability will enhance the usability of the reinforcements.

The Cellulose Nanocrystal (CNC) of dispersion condition is important factor when reinforce concrete or cement composite as CNC, because it is closely related to the strength reinforcement. Before the CNC is utilized to reinforcement of concrete or cement composite, it is essential to evaluate the dispersion properties. Therefore, the objective of the present study is to evaluate the dispersion of CNC. In this experiment, the specimen was prepared to the type of CNC suspension in accordance with weight ratio of CNC and the dispersion time of sonication. The first property, the dispersion properties of CNC, was evaluated by measuring turbidity and absorbance. The second property, the dispersion stability, was measured through the sediment time.

The purpose of this study is to investigate the optimum conditions of dispersion and strength to maximize the mechanical properties of woody cellulose nano–crystal (CNC). As a dispersing method, ultrasonic dispersing machine and magnetic stirrer were used as the mechanical dispersion method. The mixing ratio of cellulose nano-crystals (CNCs) was 0.2% and the dispersion time was 10 minutes. Steam curing was carried out for 6, 24 and 48 hours. Based on the experimental results, we will propose source technology regarding CNC for construction materials.

Gd2O3:Eu3+ red phosphors were prepared by template method from crystalline cellulose impregnated by metal salt. The crystallite size and photoluminescence(PL) property of Gd2O3:Eu3+ red phosphors were controlled by varying the calcination temperature and Eu3+ mol ratio. The nano dispersion of Gd2O3:Eu3+ was also conducted with a bead mill wet process. Dependent on the time of bead milling, Gd2O3:Eu3+ nanosol of around 100 nm (median particle size : D50) was produced. As the bead milling process proceeded, the luminescent efficiency decreased due to the low crystallinity of the Gd2O3:Eu3+ nanoparticles. In spite of the low PL property of Gd2O3:Eu3+ nanosol, it was observed that the photoluminescent property was recovered after re-calcination. In addition, in the dispersed nanosol treated at 85 oC, a self assembly phenomenon between particles appeared, and the particles changed from spherical to rod-shaped. These results indicate that particle growth occurs due to mutual assembly of Gd(OH)3 particles, which is the hydration of Gd2O3 particles, in aqueous solvent at 85 oC.

An optimum route to fabricate oxide dispersion strengthened ferritic superalloy with desired microstructure was investigated. Two methods of high energy ball milling or polymeric additive solution route for developing a uniform dispersion of Y2O3 particles in Fe-Cr-Al-Ti alloy powders were compared on the basis of the resulting microstructures. Microstructural observation revealed that the crystalline size of Fe decreased with increases in milling time, to values of about 15-20 nm, and that an FeCr alloy phase was formed. SEM and TEM analyses of the alloy powders fabricated by solution route using yttrium nitrate and polyvinyl alcohol showed that the nano-sized Y-oxide particles were well distributed in the Fe based alloy powders. The prepared powders were sintered at 1000 and 1100 oC for 30 min in vacuum. The sintered specimen with heat treatment before spark plasma sintering at 1100 oC showed a more homogeneous microstructure. In the case of sintering at 1100 oC, the alloys exhibited densified microstructure and the formation of large reaction phases due to oxidation of Al.

To improve dispersibility of cereal powder without additives, granulation of cereal powder was conducted using fluidized- bed granulator. Operation condition was sample 300 g, internal temperature 40°C, ventilation speed 30-90 m3/ h, inlet temperature 90°C and spray pressure 2.5 bar. The amount of distilled water (20-45%) as binder, granulation time (10-15 min) and drying time (3-10 min) were controlled. Mean diameter over volume (Brouckere mean, D4,3) was increased from 123 μm to 263 μm and dispersibility was improved from 73% to 92.25% at experiment conditions. Wettability (wetting time) was drastically decreased from 5,000 second to 7 second. Granulation of cereal powder did not affect sinkability and mean diameter over volume as wet analysis was about the same between raw and granulated cereals. Such phenomenon means that granulation with only water as binder enables cereal powder to disperse in water or milk without rapid sedimentation.

In the present work, we use multiwall carbon nanotubes (MWCNT) as the starting material for the fabrication of sintered carbon steel. A comparison is made with conventionally sintered carbon steel, where graphite is used as the starting material. Milling is performed using a horizontal mill sintered in a vacuum furnace. We analyze the grain size, number of pores, X-ray diffraction patterns, and microstructure. Changes in the physical properties are determined by using the Archimedes method and Vickers hardness measurements. The result shows that the use of MWCNTs instead of graphite significantly reduces the size and volume of the pores as well as the grain size after sintering. The addition of Y2O3.to the Fe-MWCNT samples further inhibits the growth of grains.

PURPOSES :This study aims to improve complex modeling of multivariable, nonlinear, and overdispersion data with an artificial neural network that has been a problem in the civil and transport sectors.METHODS :Deep learning, which is a technique employing artificial neural networks, was applied for developing a large bus fuel consumption model as a case study. Estimation characteristics and accuracy were compared with the results of conventional multiple regression modeling.RESULTS :The deep learning model remarkably improved estimation accuracy of regression modeling, from R-sq. 18.76% to 72.22%. In addition, it was very flexible in reflecting large variance and complex relationships between dependent and independent variables.CONCLUSIONS :Deep learning could be a new alternative that solves general problems inherent in conventional statistical methods and it is highly promising in planning and optimizing issues in the civil and transport sectors. Extended applications to other fields, such as pavement management, structure safety, operation of intelligent transport systems, and traffic noise estimation are highly recommended.

This study investigates the oxidation properties of Fe-14Cr ferritic oxide-dispersion-strengthened (ODS) steel at various high temperatures (900, 1000, and 1100°C for 24 h). The initial microstructure shows that no clear structural change occurs even under high-temperature heat treatment, and the average measured grain size is 0.4 and 1.1 μm for the as-fabricated and heat-treated specimens, respectively. Y–Ti–O nanoclusters 10–50 nm in size are observed. High-temperature oxidation results show that the weight increases by 0.27 and 0.29 mg/cm2 for the asfabricated and heat-treated (900°C) specimens, and by 0.47 and 0.50 mg/cm2 for the as-fabricated and heat-treated (1000°C) specimens, respectively. Further, after 24 h oxidation tests, the weight increases by 56.50 and 100.60 mg/cm2 for the as-fabricated and heat-treated (1100°C) specimens, respectively; the latter increase is approximately 100 times higher than that at 1000°C. Observation of the surface after the oxidation test shows that Cr2O3 is the main oxide on a specimen tested at 1000°C, whereas Fe2O3 and Fe3O4 phases also form on a specimen tested at 1100°C, where the weight increases rapidly. The high-temperature oxidation behavior of Fe-14Cr ODS steel is confirmed to be dominated by changes in the Cr2O3 layer and generation of Fe-based oxides through evaporation.

Well-dispersed platinum catalysts on ruthenium oxide nanofiber supports are fabricated using electrospinning, post-calcination, and reduction methods. To obtain the well-dispersed platinum catalysts, the surface of the nanofiber supports is modified using post-calcination. The structures, morphologies, crystal structures, chemical bonding energies, and electrochemical performance of the catalysts are investigated. The optimized catalysts show well-dispersed platinum nanoparticles (1-2 nm) on the nanofiber supports as well as a uniform network structure. In particular, the well-dispersed platinum catalysts on the ruthenium oxide nanofiber supports display excellent catalytic activity for oxygen reduction reactions with a half-wave potential (E1/2) of 0.57 V and outstanding long-term stability after 2000 cycles, resulting in a lower E1/2 potential degradation of 19 mV. The enhanced electrochemical performance for oxygen reduction reactions results from the well-dispersed platinum catalysts and unique nanofiber supports.

Garment skin leather 표면 코팅에 사용된 폴리우레탄 수지는 polyethylene glycole(PEG)의 함유를 [NCO]/[OH] mole % 비로 달리하면서 합성하였으며, 합성된 폴리우레탄 수지의 기계적 특성은 SEM, FT-IR, UTM 등을 이용하여 측정하였다. 비이온성을 띄고 있는 PEG(poly ethylene glycol)의 [NCO]/[OH] mole % 비가 증가함에 따라 내굴곡성(건식, 습식)의 변화는 없었으며, 내마모도, 인장강 도수치가 낮아짐을 알 수 있었다. 반대로 연신율 물성은 증가함을 알 수 있었다. 점도 변화 측정 결과에 는 PEG의 [NCO]/[OH] mole % 증가에 따라 점도가 묽어짐을 알 수 있었다.

Nanosized and aggregated Y2O3:Eu Red phosphors were prepared by template method from metal salt impregnated into crystalline cellulose. The particle size and photoluminescent property of Y2O3:Eu red phosphors were controlled by variation of the calcination temperature and time. Dispersed nanosol was also obtained from the aggregated Y2O3:Eu Red phosphor under bead mill wet process. The dispersion property of the Y2O3:Eu nanosol was optimized by controlling the bead size, bead content ratio and milling time. The median particle size (D50) of Y2O3:Eu nanosol was found to be around 100 nm, and to be below 90 nm after centrifuging. In spite of the low photoluminescent properties of Y2O3:Eu nanosol, it was observed that the photoluminescent property recovered after re-calcination. The dispersion and photoluminescent properties of Y2O3:Eu nanosol were investigated using a particle size analyzer, FE-SEM, and a fluorescence spectrometer.

Zirconia nanoparticles were widely used as filler in order to get high refractive index layer. However, dispersion of nanoparticles is difficult due to their agglomeration in solvent. In this study, the dispersibility of the zirconia suspension is promoted by controlling the steric hindrance and electrostatic interactions through the adsorption of PEI according to alkali treatment time. Also, to induce improved dispersibility on suspension, we changed the dispersion conditions variously and fabricated an ink formulation method for the coating layer. Zirconia suspension was characterized by dynamic light scattering (DLS), Zeta potential measurement, Transmission Electron Microscope (TEM) and FT-IR. We were able to confirm that good dispersion of zirconia suspension by alkali treatment and PEI led to high refractive index.

Magnesium alloy is becoming known for the lightest material in the metallic materials. Recently the automotive industry has a variety application to the light weight parts replacement. This study focuses on the mechanical property improving through a tiny amount’s CNT addition into the magnesium alloy as AM60. The CNT material is an arduous combination of the metallic materials. Therefore this study is concentrating on the contact force growth for the CNT material. Consequently, the made CNT is produced by the CVD process using the magnesium catalyst. The CNT material has dispersive with mechanical process into the molten AM60 alloy. The mechanical experiment result that hardness is 18% increasing and tensile strength is 13% increasing, better than the raw AM60 alloy on this investigation.

Al2O3 nanosol dispersed under ethanol or N-Methyl-2-pyrrolidone(NMP) was studied and optimized with various dispersion factors and by utilizing the silane modification method. The two kinds of Al2O3 powders used were prepared by thermal decomposition method from aluminum ammonium sulfate(AlNH4(SO4)2) while controlling the calcination temperature. Al2O3 sol was prepared under ethanol solvent by using a batch-type bead mill. The dispersion properties of the Al2O3 sol have a close relationship to the dispersion factors such as the pH, the amount of acid additive(nitric acid, acetic acid), the milling time, and the size and combination of zirconia beads. Especially, Al2O3 sol added 4 wt% acetic acid was found to maintain the dispersion stability while its solid concentration increased to 15 wt%, this stability maintenance was the result of the electrostatic and steric repulsion of acetic acid molecules adsorbed on the surface of the Al2O3 particles. In order to observe the dispersion property of Al2O3 sol under NMP solvent, Al2O3 sol dispersed under ethanol solvent was modified and solventexchanged with N-Phenyl-(3-aminopropyl)trimethoxy silane(APTMS) through a binary solvent system. Characterization of the Al2O3 powder and the nanosol was observed by XRD, SEM, ICP, FT-IR, TGA, Particles size analysis, etc.

The sol-gel method is the simplest method for synthesizing monodispersed silica particles. The purpose of this study is to synthesize uniform, monodisperse spherical silica nanoparticles using tetraethylorthosilicate (TEOS) as the silica precursor, ethanol, and deionized water in the presence of ammonia as a catalyst. The reaction time and temperature and the concentration of the reactants are controlled to investigate the effect of the reaction parameters on the size of the synthesized particles. The size and morphology of the obtained silica particles are investigated using transmission electron microscopy and particle size analysis. The results show that monodispersed silica particles over a size range of 54-504 nm are successfully synthesized by the sol-gel method without using any additional process. The nanosized silica particles can be synthesized at higher TEOS/H2O ratios, lower ammonia concentrations, and especially, higher reaction temperatures.

결정성 탄소물질은 결합의 형태에 따라 carbyne (sp1, 1D 구조), graphite (sp2+π, 2D), diamond (sp3, 3D) 구조 로 나뉜다. 특히 sp2 결합에 기반한 나노물질은 fullerene (0D), 탄소나노튜브 (1D or quasi-2D), 그래핀 (2D) 으로 나뉜 다. 탄소나노튜브와 그래핀은 물리적으로 여러 가지 뛰어난 특성이 있어 구조재나 광전자 재료, 멤브레인 등 다양한 분 야에 응용가치가 높다. 하지만 이들 나노재료는 강하게 응집되는 성질이 있어 용액에 분산할 필요가 있다. 특히 이는 용 액 상에서 박리, 안정화의 과정을 거쳐야 안정적으로 분산된 상태를 유지할 수 있다. 본 고에서는 탄노나노튜브나 그래 핀이 용매에서 박리되어

본 연구의 목적은 트리아세테이트와 흡한속건성 PET 합연사로 구성된 복합직물의 염착량 증진 및 동일색상 염색 (union dyeing)을 위한 최적 혼합염색 조건을 찾는 것이다. 이를 위하여 E-type 분산염료(C.I. Disperse red 50)와 S-type 분산염료(C.I. Disperse red 92)를 혼합하여 1욕 혼합염색으로 염색온도, 염색시간, 염료의 혼합비율에 따른 염색직물의 흡진율, 염착율, 색상 및 색차를 측정하였다. 혼합염색의 염착평형은 100℃에서 일어났으나 염색된 직물의 K/S 값과 겉보기 색상을 비교해보았을 때 트리아세테이트와 흡한속건성 PET의 색이 동일한 색으로 발현되는 온도는 120℃임을 확인하였다. 염색 시간 증가에 따른 혼합염료 흡진율과 염착량의 변화는 크게 나타나지 않았으나 염색시간이 길수록 그리고 혼합염료를 사용할 경우 균일한 색상을 얻을 수 있었다. E-type에 S-type염료의 혼합비율을 적절히 조절하여 혼합염색 하면 단독염색 보다 E-type 염료의 색상과 차이 없이 염착량을 증대시킬 수 있었다.