Effects of the amount of nickel powder (Ni) in Ni-carbon fiber (CF) hybrid filler systems on the conductivity(or resistivity) and thermal coefficient of resistance (TCR) of filled high density polyethylene were studied. Increases of the resistivity and TCR with increasing Ni concentration at a given hybrid filler content were observed. Using the fiber contact model, we showed that the main role of Ni in the hybrid filler system is to decrease the interfiber contact resistance when Ni concentration is less than the threshold point. The formation of structural defects leading to reduced reinforcing effect resulted in both a reduction of strength and an increase of the coefficient of thermal expansion in the composite film; these changes are responsible for the increases of both resistivity and TCR with increasing Ni concentration in the hybrid filler system.

This study involves using nickel chloride solution as a raw material to produce nano-sized nickel oxide powder with average particle size below 50 nm by the spray pyrolysis reaction. The influence of the inflow speed of raw material solution on the properties of the produced powder is examined. When the inflow speed of the raw material solution is at 2 ml/min., the average particle size of the powder is 15~25 nm and the particle size distribution is relatively uniform. When the inflow speed of the solution increases to 10 ml/min., the average particle size of the powder increases to about 25 nm and the particle size distribution becomes much more uneven. When the inflow speed of the solution increases to 20 ml/min., the average particle size of the powder increases in comparison to the case in which the inflow speed of the solution was 10 ml/min. However, the particle size distribution is very uneven, showing various particle size distributions ranging from 10 nm to 70 nm. When the inflow speed of solution increases to 50 ml/min., the average particle size of the powder decreases in comparison to the case in which the inflow speed was 20 ml/min., and the particle size distribution shows more evenness. As the inflow speed of the solution increases from 2 ml/min. to 20 ml/min., the XRD peak intensities gradually increase, while the specific surface area decreases. When the inflow speed of solution increases to 50 ml/min., the XRD peak intensities rather decrease, while the specific surface area increases.

In this study, fine cathode materials and were synthesized using the simple, convenient process of mechanical alloying (MA). In order to improve the cell properties, wet milling processes were conducted using low-energy ball milling to decrease the mean particle size of both materials. The cells of Na/ and Na/ show a high initial discharge capacity of 425 mAh/g and 577 mAh/g respectively using wet milled powder particles, which is much larger than commercial ones, providing some potential as new cathode materials for rechargeable sodium-ion batteries.

The electrochemistry characterization of metal is important in many industrial applications. In this study, we investigated the C-V diagrams related to the electrochemistry characterization of nickel. We determined electrochemical measurement by using cyclic voltammetry with a three electrode system. A measuring range was reduced from initial potential to -1350mV, continuously oxidized to 1650mV and measured to the initial point. The scan rate were 100, 150, 200 and 200mV/s. As a result, the C-V characterization of nickel using ethanolamine and ethylethanolamine inhibitor appeared irreversible process caused by the oxidation current from the cyclic voltammogram. After adding ethanolamine compound additive, adsorption film constituted, and the passive phenomena happened. According to the results by cyclic voltammetry method, it was revealed that the effect of the electrochemistry characterization of nickel depends on ethanolamine structure interaction to adsorption complex.

A porous nickel-tin nano-dendritic electrode, for use as the anode in a rechargeable lithium battery, has been prepared by using an electrochemical deposition process. The adjustment of the complexing agent content in the deposition bath enabled the nickel-tin alloys to have specific stoichiometries while the amount of acid, as a dynamic template for micro-porous structure, was limited to a certain amount to prevent its undesirable side reaction with the complexing agent. The ratios of nickel to tin in the electro-deposits were nearly identical to the ratios of nickel ion to tin ion in the deposition bath; the particle changed from spherical to dendritic shape according to the tin content in the deposits. The nickel to tin ratio and the dendritic structure were quite uniform throughout the thickness of the deposits. The resulting nickel-tin alloy was reversibly lithiated and delithiated as an anode in rechargeable lithium battery. Furthermore, the resulting anode showed much more stable cycling performance up to 50 cycles, as compared to that resulting from dense electro-deposit with the same atomic composition and from tin electrodeposit with a similar porous structure. From the results, it is expected that highly-porous nickel-tin alloys presented in this work could provide a promising option for the high performance anode materials for rechargeable lithium batteries.

Nickel recovery method was studied by the wet process from the catalyst used in hydrogenation process. Nickel content in waste catalyst was about 16%. At the waste catalyst leaching system by the alkaline solution, selective leaching of nickel was possible by amine complex formation reaction from ammonia water and ammonium chloride mixed leachate. The best leaching condition of nickel from mixed leachate was acquired at the condition of pH 8. LIX65N as chelating solvent extractant was used to recover nickel from alkaline leachate. The purity of recovered nickel was higher than 99.5%, and the whole quantity of nickel was recovered from amine complex.

본 논문에서는 6,13-bis (triisopropylsily lethynyl)-pentacene (TIPS-pentacene) 유기 박막 트랜지스터에 니켈 버퍼층을 적층했을 때의 효과를 연구하였다. 니켈 (Nickel) / 은(Silver) 소스 드레인 전극은 은 (Silver) 전극이 단독으로 쓰일 때 보다 에너지 레벨차이를 줄여 캐리어의 주입이 더 잘되도록 도와주므로써 전기적 특성을 향상 시켜준다. 또한 유기 게이트 절연체의 추가로 TIPS-pentacene 은 규칙적 배열된 형태를 가지므로써 소자 성능의 향상을 가지고 온다. 제작한 유기박막트랜지스터 에서 0.01 cm2의 포화영역 이동도를 얻을 수 있었으며, 또한 드레인 전압을 50 V로 하고 게이트 전압을 20 V에서 -50 V 까지 인가하였을 때 2×104의 전멸 비를 얻을 수 있었다. 이러한 결과를 polyethylene terephthalate (PET) 기판을 이용한 유연한 OTFTs 에 적용시켜본 결과 유리기판위에 제작했을 때와 비슷한 성능을 얻음을 확인하였다.

Disk type porous nickel membrane was fabricated by in-situ reduction/sintering process using compacted NiO/PMMA (PMMA; Polymethyl methacrylate) mixture at 800℃ in hydrogen atmosphere. The porosity (4958%) of these membrane was investigated as an amount of PMMA additive. The thermal decomposition and reduction behavior of NiO/PMMA were analyzed by TG/DTA in hydrogen atmosphere and the activation energy for the hydrogen reduction of NiO and thermal degradation of PMMA was calculated as 61.1 kJ/mol, evaluated by Kissinger method. Finally, the filtering performance and pressure drop were measured by particle counting system.

Lotus-type porous nickel with cylindrical pores was fabricated by unidirectional solidification under an Ar gas atmosphere using the thermal decomposition method of the compounds such as sodium hydroxide, calcium hydroxide, calcium carbonate, and titanium hydride. The decomposed gas does form the pores in liquid nickel, and then, the pores become the cylindrical pores during unidirectional solidification. The decomposed particles from the compounds do play a rule on nucleation sites of the pores. The behavior of pore growth was controlled by atmosphere pressure, which can be explained by Boyle's law. The porosity and pore size decreased with increasing Ar gas pressure when the pores contain hydrogen gas decomposed from calcium and sodium hydroxide and titanium hydride, ; however it they did not change when the pores contain containing carbon dioxide decomposed from calcium carbonate. These results indicate that nickel does not have the solubility of carbon dioxide. Lotus-type porous metals can be easily fabricated by the thermal decomposition method, which is superior to the conventional fabrication method used to pressurized gas atmospheres.

We fabricated thermally evaporated 30 nm-Ni/(20 nm or 60 nm)a-Si:H/Si films to investigate the energy-saving property of silicides formed by rapid thermal annealing (RTA) at temperatures of 350˚C, 450˚C, 550˚C, and 600˚C for 40 seconds. A transmission electron microscope (TEM) and a high resolution X-ray diffractometer (HRXRD) were used to determine the cross-sectional microstructure and phase changes. A UVVIS-NIR and FT-IR (Fourier transform infrared spectroscopy) were employed for near-IR and middle-IR absorbance. Through TEM and HRXRD analysis, for the nickel silicide formed at low temperatures below 450˚C, we confirmed columnar-shaped structures with thicknesses of 20~30 nm that had δ-Ni2Si phases. Regarding the nickel silicide formed at high temperatures above 550˚C, we confirmed that the nickel silicide had more than 50 nm-thick columnar-shaped structures with a Ni31Si12 phase. Through UV-VIS-NIR analysis, nickel silicide showed almost the same absorbance in the near IR region as well as ITO. However, in the middle IR region, the nickel silicides with low temperature showed similar absorbance to those from high temperature silicidation.

In this work, we employed an electroless nickel plating on glass fibers in order to enhance the electric conductivity of fibers. And the effects of metal content and plating time on the conductivity of fibers were investigated. From the results, island-like metal clusters were found on the fiber surfaces in initial plating state, and perfect metallic layers were observed after 10 min of plating time. The thickness of metallic layers on fiber surfaces was proportion to plating time, and the electric conductivity showed similar trends. The nickel cluster sizes on fibers decreased with increasing plating time, indicating that surface energetics of the fibers could become more homogeneous and make well-packed metallic layers, resulting in the high conductivity of Ni/glass fibers.

In the present study Sisal fiber obtained from the leaves of Agave sisalana has been chosen to validate its viability as an adsorbent for the removal of Nickel from aqueous solutions. The material was also surface modified and its effect on adsorption of Nickel was also studied. Agave sisalana fiber was found to be a cheap and effective adsorbent doing away with the need to activate the material therby reducing processing cost. The equilibrium studies indicated that the adsorption capacity of raw fiber and the surface modified fiber was 8.66 and 9.77 mg/g respectively with the Langmuir isotherm describing the adsorption phenomena better than the Freundlich and Temkin isotherm. The adsorption was found to be exothermic from the thermodynamic studies and the kinetics showed that the adsorption phenomena were second order.

As a fundamental study for chronic test (definitive test), the range finding test must have been done prior to conducting chronic test. The aims of this study were 1) to search the effective concentration range of two different heavy metals (cadmium and nickel) to indigenous collembolan species (Paranura rosea) 2) to compare the toxicity of cadmium and nickel depending on exposure durations. Toxicity tests were conducted in accordance with the standardized toxicity test proposed by OECD. In this study, there were no mortality occurred at all test concentrations for 7-days exposure. In contrast to 7-days exposure, there were slight increases in mortalities were observed at the concentration higher than 400 mg/kg for both heavy metals for 14-days exposure. The estimated LC50s for cadmium and nickel were 3980.65 (2036.08-64668.61) and 1597.85 (1087.87-3817.61) mg/kg, respectively. The results of this study may be used as a fundamental toxicity data for two heavy metals to proceed in chronic test in the future study.

수수(Sorghum bicolor(L.) Moench) 잡종의 미량(微量) 광물질(鑛物質) 함량에 미치는 정수장(淨水場) 슬러지의 영향에 관해 조사를 했는데, 이번 보고는 니켈 성분의 분석에 관한 것이다. 대조구(對照區), 부숙(腐熟)시킨 정수장 슬러지, 정수장 슬러지+질소－인산－칼륨 비료, 부숙시킨 슬러지+질소, 인산, 칼륨 비료의 4가지를 처리로 하였고, 1, 3, 5시간 예열(豫熱) 시간이 실험 조건이었다. 5시간 이후의 조건에서 백그라운드의 값이

Thermally evaporated 10 nm-Ni/1 nm-Au/(30 nm-poly)Si structures were fabricated in order to investigate the thermal stability of Au-inserted nickel silicide. The silicide samples underwent rapid thermal annealing at 300~1100˚C for 40 seconds. The sheet resistance was measured using a four-point probe. A scanning electron microscope and a transmission electron microscope were used to determine the cross-sectional structure and surface image. High-resolution X-ray diffraction and a scanning probe microscope were employed for the phase and surface roughness. According to sheet resistance and XRD analyses, nickel silicide with Au had no effect on widening the NiSi stabilization temperature region. Au-inserted nickel silicide on a single crystal silicon substrate showed nano-dots due to the preferred growth and a self-arranged agglomerate nano phase due to agglomeration. It was possible to tune the characteristic size of the agglomerate phase with silicidation temperatures. The nano-thick Au-insertion was shown to lead to self-arranged microstructures of nickel silicide.