The study on the fabrication of iron powder from forging scales using hydrogen gas has been conducted on the effect of hydrogen partial pressure, temperature, and reactive time. The mechanism for the reduction of iron oxides was proposed with various steps, and it was found that reduction pattern might be different depending on tem- perature. The iron content in the scale and reduction ratio of oxygen were both increased with increasing reactive time at 0.1atm of hydrogen partial pressure. On the other hand, for over 30 minutes at 0.5 atm of hydrogen partial pressure, the values were found to be almost same. In the long run, iron metallic powder was obtained with over 90% of iron content and an average size of its powder was observed to be about 100 µm.

The extraction of metallic pure vanadium powder from raw oxide has been tried by Mg-reduction. In first stage, powders as initial raw material was reduced by hydrogen gas into phase. powder was reduced in next stage by magnesium gas at 1,073K for 24 hours. After reduction reaction, the MgO component mixed with reduced vanadium powder were dissolved and removed fully in 10% HCl solution for 5 hours at room temperature. The oxygen content and particle size of finally produced vanadium powders were 0.84 wt% and 1 , respectively

The ultra-fine and less agglomerated titanium carbonitride particles were successfully synthesized by magnesiothermic reduction with low feeding rate of solution. The sub-stoichiometric titanium carbide () particles were produced by reduction of chlorine component by liquid magnesium at of gaseous and the heat treatments in vacuum were performed for 5 hours to remove the residual magnesium and magnesium chloride mixed with produced . The final particle with near 100 nm in mean size and high specific surface area of was obtained by nitrification under nitrogen gas at for 2 hrs.

A novel chemical method was evaluated to fabricate the ultrafine tungsten heavy alloy powders with bater-base solution made from the ammonium metatungstate (AMT), iron(II) chloride tetrahydrate (), nickel(II) chloride hexahydrate () as source materials and the sodium tungstate dihydrate () as Cl-reductant. In the preparation of mixtures the amounts of the source components were chosen so as to obtain alloy of 93W-5Ni-2Fe composition(wt.%). The obtained powders were characterized by X-ray diffraction, XRF, field-emission scanning microscope (FESEM), and chemical composition was analyzed by EDX.

일본은 외무성 홈페이지에서 삼국사기 기록에 의하면 우산국이었던 울릉도가 512년 신라에 귀속되게 되었음을 알려주는 기술은 있으나 우산도에 관한 언급은 없다고 주장한다. 이에 대해 한일양국의 많은 자료는 “울릉도와 우산도(독도)가 지리적으로 인접한 섬이며, 우산도는 울릉도의 부속도서이다”라는 것을 기록을 통해 쉽게 추정해 볼 수 있다. 따라서 우산도는 울릉도의 부속도서임이 분명하다. 그리고 종물은 주물의 처분에 따른다는 부종성의 원칙에 따라 우산도는 울릉도와 운명을 같이 한다. 삼국사기 기록에 신라 지증왕 13년(512년)에 울릉도가 이사부에 의하여 신라에 복속되었다면 우산도 또한 신라에 복속된 것이다. 따라서 일본의 두 섬이 별개라는 주장은 타당한 근거에 의한 주장이 아니다. 울릉도와 우산도가 신라에 복속되는 과정에서 신라의 영토 취득 형태는 정복에 해당한다. 이는 당시의 영토취득 방법 중 하나로 정당하다. 그러나 오늘의 국제법 상은 인정되는 방법은 아니다. 그리고 현대 국제법 이전의 역사적 권원은 현대 국제법에 의하여 대체되지 않으면 현대 국제법상 효력이 없다. 이사부의 우산국 정벌로 인한 신라의 영토취득은 역사적 권원에 해당한다. 따라서 신라의 영토취득이 현대 국제법에 의하여 효과를 나타내기 위해서는 권원의 대체가 필요하다. 여기에 관해서는 신라의 우산국의 복속 및 그 이후의 고려, 조선, 대한제국에 의해 순차적으로 승계되어 오던 중 1900년 10월 대한제국 칙령 제41호 공포로 권원의 대체가 이루졌다고 본다. 이는 현대 국제법에 의해서도 독도를 우리 땅이라 주장할 정당한 근거이다. 따라서 독도는 우리 땅이다.

Zr-Ti alloy powders were successfully synthesized by magnesium thermal reduction of metal chlorides. The evaporated and mixed gasses of were injected to liquid magnesium and the chloride components were reduced by magnesium leading to the formation of . The released Zr and Ti atoms were then condensed to particle forms inside the mixture of liquid magnesium and magnesium chloride, which could be dissolved fully in post process by 1~5% HCl solution at room temperature. By the fraction-control of individually injected and gasses, the final compositions of produced alloy powders were changed in the ranges of Zr-0 wt.%~20 wt.%Ti and their purity and particle size were about 99.4% and the level of several micrometers, respectively.

Titanium carbonitride is more perspective materials compared to titanium carbide. It can be used in tool industry and special products because of its higher strength, abrasive wear-resistance and especially its strong chemical stability at high temperatures. We produced STS+TiCxNy composite by the spark plasma sintering for higher strength and studied the characteristics. The planar and cross-sectional microstructures of the specimens were observed by scanning electron microscopy. Characterizations of the carbon and nitride phases on the surface of composite were carried out using an X-ray diffractometer. During annealing TiCxNy particles diffusion into STS 430 was observed. After annealing, sintering isolations between particles were formed. It causes decreasing of mechanical strength. In addition when annealing temperature was increased hardness increased. Heterogeneous distribution of alloying elements particles was observed. After annealing composites, highest value of hardness was 738.1 MHV.

Titanium powders have been usually produced by de-hydrogenating treatment in vacuum with titanium hydride () powders prepared by milling of hydrogenated sponge titanium, . The higher stoichiometry of x in , whose maximum value is 2, is achieved, crushing behavior is easier. powder can be, therefore, easy to manufactured leading to obtain higher recovery factor of it. In addition, contamination of the powder can also minimized by the decrease of milling time. In this study, the hydrogenation behavior of sponge titanium was studied to find the maximum stoichiometry. The maximum stoichiometry in hydride formation of sponge titanium could be obtained at for 2 hrs leading to the formation of and the treating temperatures lower or higher than caused the poor stoichiometries by the low hydrogen diffusivity and un-stability of , respectively. Such experimental behavior was compared with thermodynamically calculated one. The hydrogenated sponge was fully ball-milled under -325 Mesh and the purity of pure titanium powders obtained by de-hydrogenation was about 99.6%.

The ultrafine titanium carbonitride () particles below 100 nm in mean size, including various carbon and nitrogen contents (x=0.55~0.9, y=0.1~0.5), were successfully synthesized by new Mg-thermal reduction process. Nanostructured sub-stoichiometric titanium carbide () particles were initially produced by the magnesium reduction of gaseous at and post heat treatments in vacuum were performed for 2 hrs to remove residual magnesium and magnesium chloride mixed with . Finally, well C/N-controled phases were successfully produced by nitrification heat treatment under normal gas atmosphere at for 2 hrs. The values of purity, mean particle size and oxygen content of produced particles were about 99.3%, 100 nm and 0.2 wt.%, respectively.

HDDR treated anisotropic Nd-Fe-B powders have been widely used for the sheet motors and the sunroof motors of hybrid or electric vehicles, due to their excellent magnetic properties. Microstructural alignment of HDDR treated powders are mostly depending on the hydrogen reaction in disproportionation step, so the specific method to control hydrogenation reaction is required for improving magnetic properties. In disproportionation step, hydrogenation pressure and reaction time were controlled in the range of 0.15~1.0 atm for 15~180 min in order to control the micorstructural alignment of phase and, at the same time, to improve remanence of HDDR treated magnet powders. In this study, we could obtain a well aligned anisotropic Nd-Fe-B-Ga-Nb alloy powder having high remanence of 12 kG by reducing hydrogen pressure down to 0.3 atm in disproportionation step.

HDDR treated anisotropic Nd-Fe-B powders have been widely used, due to their excellent magnetic properties, especially for sheet motors and sunroof motors of hybrid and electric vehicles. Final microstructure and coercivity of such Nd-Fe-B powders depend on the state of starting mother alloys, so additional homogenization treatment is required for improving magnetic properties of them. In this study, a homogenization treatment was performed at in order to control the grain size and Nd-rich phase distribution, and at the same time to improve coercivity of the HDDR treated magnetic powders. FE-SEM was used for observing grain size of the HDDR treated powder and EPMA was employed to observe distribution of Nd-rich phase. Magnetic properties were analyzed with a vibrating sample magnetometer.

Web usability for e-commerce sites becomes a more important issue as e-commerce gains its popularity. As for agricultural products, consumers are especially sensitive to the quality of information during transaction process. Successful e-commerce sites of agricultural products, such as Wine.com and Tesco, identified regular usability testing as part of key success factors. This paper aims to identify processes for evaluating usability for e-commerce sites of agricultural products and provide strategies to improve usability. The study aims to evaluate e-commerce usability of selected e-commerce sites using heuristic evaluation to provide objective e-commerce sites usability analysis for each transaction process.

The ultrafine titanium carbonitride particles () below 100nm in mean size were successfully synthesized by Mg-thermal reduction process. The nanostructured sub-stoichiometric titanium carbide () particles were produced by the magnesium reduction at 1123K of gaseous and the heat treatments in vacuum were performed for five hours to remove residual magnesium and magnesium chloride mixed with . And final phase was obtained by nitrification under normal gas at 1373K for 2 hrs. The purity of produced particles was above 99.3% and the oxygen contents below 0.2 wt%. We investigated in particular the effects of the temperatures in vacuum treatment on the particle refinement of final product.

Nano-sized tungsten disulfide () powders were synthesized by chemical vapor condensation (CVC) process using tungsten carbonyl () as precursor and vaporized pure sulfur. Prior to the synthesis of tungsten disulfide nanoparticles, the pure tungsten nanoparticles were produced by same route to define the optimum synthesis parameters, which were then successfully applied to synthesize tungsten disulfide. The influence of experimental parameters on the phase and chemical composition as well as mean size of the particles for the produced pure tungsten and tungsten disulfide nanoparticles, were investigated

Ordered to FePt nanoparticles are strong candidates for high density magnetic data storage media because the phase FePt has a very high magnetocrystalline anisotropy , high coercivity and chemical stability. In this study, the ordered FePt nanoparticles were successfully fabricated by chemical vapor condensation process without a post-annealing process which causes severe particle growth and agglomeration. The nanopowder was obtained when the mixing ratio of Fe(acac) and Pt(arac) was 2.5 : 1. And the synthesized FePt nanoparticles were very fine and spherical shape with a narrow size distribution. The average particle size of the powder tended to increase from 5 nm to 10 nm with increasing reaction temperature from to . Characterisitcs of FePt nanopowder were investigated in terms of process parameters and microstructures.

  Recently, the control chart is developed for monitoring processes with normal short production runs by the coefficient of variation(CV) characteristic for a normal distribution. This control chart does not work well in non-normal short production runs.

The nanostructured cerium oxide powders were synthesized by spray thermal decomposition process for the use as the raw materials of resistive oxygen sensor. The synthesis routes consisted of 1) spray drying of water based organic solution made from cerium nitrate hydrate () and 2) heat treatment of spray dried precursor powders at in air atmosphere to remove the volatile components and identically to oxidize the cerium component. The produced powders have shown the loose structure agglomerated with extremely fine cerium oxide particles with about 15 nm and very high specific surface area (). The oxygen sensitivity, n ( and the response time, measured at in the sample sintered at , were about 0.25 and 3 seconds, respectively, which had much higher performances than those known in micron or sized sensors.