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Free Volume Formation in Amorphous Alloys: a Molecular Dynamics Study
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이창면 Chang Myeon Lee , 박경원 Kyoung Won Park , 이병주 Byeong Joo Lee , 심재혁 Jae Hyeok Shim , 이재훈 Jae Hoon Lee , 이재철 Jae Chul Lee |
KJMM 46(11) 701-707, 2008 |
ABSTRACT
This study examined the creation mechanism of free volume during homogeneous deformation induced by the elastostatic compression at room temperature. Experiments demonstrated that amorphous alloys subjected to the elastostatic compression underwent structural disordering, during which densely packed polyhedra breakdown to form new, loosely packed ones, resulting in the creation of excess free volume. A combination of experiments and molecular dynamics simulations are used to explore fundamental issues on how free volume is created during elastostatic compression.
keyword : amorphous alloys, free volume, structural disorder, molecular dynamics
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A Study on the High Temperature Gas Nitriding Heat Treatment of STS 347 and STS 310S Austenitic Stainless Steel
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유대경 Dae Kyoung Yoo , 공정현 Jung Hyun Kong , 이해정 Hea Joeng Lee , 성장현 Jang Hyun Sung , 이해우 Hae Woo Lee |
KJMM 46(11) 708-712, 2008 |
ABSTRACT
The influence of high temperature gas nitriding (HTGN) in STS347 and STS310S steels was experimentally investigated. The HTGN was carried out at 1,050℃~1,150℃ for 10 hrs in a gaseous atmosphere containing 1 kg/mm2 of nitrogen. After HTGN, fine precipitates of Cr2N and NbN appeared in austenite on the surface of STS 347, while nitrogen pearlite, which was layeredof Cr2N and austenite alternatively, appeared in austenite on the surface of STS 310S. The surface hardness of HTGN-treated, STS 347 and STS 310S specimens was 250~360 Hv and 270~400 Hv, respectively, depending on the temperature of HTGN. The nitrogen content was analyzed 1.4 wt% and 1.6 wt% at the surface layer of STS 347 and STS 310S steels, respectively. In addition, an improvement in the corrosion resistance of HTGN treated specimens was observed.
keyword : HTGN, High Temperature Gas Nitriding, STS 347, STS310S, Cr2N nitride
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The Effect of Mo and Cr addition on the Deep Drawability of Dual Phase Steel Sheets
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한성호 Seong Ho Han , 안연상 Yeon Sang Ahn , 진광근 Kwang Geun Chin , 김인배 In Bae Kim |
KJMM 46(11) 713-724, 2008 |
ABSTRACT
The need to lower the weights of automotive vehicle and to improve the safety of cars has resulted in the development of high strength steels such as TRIP(Transformation Induced Plasticity) and DP (Dual Phase) steel. It is well known that the higher strength of steel shows the poorer press formability. Among the high strength steels, DP steel shows several good characteristics such as low yield ratio, high initial n value, high elongation, high bake hardenability and anti-aging property. However, there`s a certain limit in application of DP steels to the automotive panel parts because their poor deep drawbility caused by martensite. In this study, the effect of alloying elements on the deep drawability and recrystallization texture in TS 440MPa grade DP steel with 0.015~0.02% carbon has been investigated on the base of SEM, TEM, XRD and EBSD analysis.
keyword : high strength steel, dual phase steel, deep drawability, recrystallization texture
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The Effect of Complexing Agents on the Deposit Characteristics in the Electroless Nickel-Tungsten-Phosphorus Plating
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조진기 Jin Ki Cho , 박상욱 Sang Wook Park , 강성군 Seung Goon Kang , 손성호 Seong Ho Son |
KJMM 46(11) 725-729, 2008 |
ABSTRACT
Deposition characteristics of electroless plated Ni-W-P films were investigated for various complexing agents. Used complexing agents are sodium citrate, sodium gluconate and sodium malonate. In this study, the existing mixed potential theory could explain the overall mechanism of Ni-W-P electroless plating for all complexing agents. The deposition rate could be also expected by the theory. The deposited Ni- W-P films were evaluated in term of surface hardness and corrosion resistance. Microhardness of the deposit increased about 1,000 Hv after heat treatment for one hour at 400℃, because it was above the crystallization temperature of Ni3P. The deposited Ni-W-P films can exhibit excellent corrosion resistance in using sodium malonate as a complexing agent, the other hand the using sodium gluconate was the worst corrosion resistance. The worst corrosion resistance was due to a large number of nano-sized pin-holes or small pores. The plating current at the mixed potential increases when the using sodium malonate as a complexing agent, it was explained by the cross section.
keyword : electroless deposit, complexing agent, mixed potential, surface hardness, corrosion resistance
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Growth Behaviors of Anodic Titanium Oxide Nanotubes in the Ethylene Glycol Solution According to Water Contents
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이병관 Byung Gwan Lee , 이성은 Seong Eun Lee , 최진욱 Jin Wook Choi , 정용수 Yong Soo Jeong , 오한준 Han Jun Oh , 이오연 Oh Yeon Lee , 지충수 Choong Soo Chi |
KJMM 46(11) 730-736, 2008 |
ABSTRACT
TiO2 nanotubes fabricated in aqueous HF-based electrolytes have been generally grown only to about 500nm in length because of the strong dissolubility of HF acid. In this paper, ethylene glycol solution has been applied for increasing the length of the anodic TiO2 nanotubes, and the growth behaviors of the nanotubes according to water contents has been investigated. Anodization of Ti in ethylene glycol+1 wt% NH4F (EG solution) with water additions up to 10 wt% were carried out at the constant voltage of 20 V. The results show that a thin titanium oxide layer is formed in the initial stage and the nanotube structure grows underneath the initial layer. And the length of TiO2 nanotubes decreases with the increasing water content in the solution. It can be ascribed to the locally acidified circumstance around the barrier layer inside the nanopore due to H+ ion originated from water. The XPS for the nanotubes suggests that the spectra of Ti2p and O1s are the major chemical bonding states of the TiO2, and those for F1s, N1s and C1s come from the compound of (NH4)2TiF6.
keyword : TiO2, nanotube, anodization, titanium dioxide, ethylene glycol
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Mechanism Study of Sticking Occurring during Hot Rolling of Ferritic Stainless Steel
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하대진 Dae Jin Ha , 성효경 Hyo Kyung Sung , 이성학 Sung Hak Lee , 이종석 Jong Seog Lee , 이용득 Yong Deuk Lee |
KJMM 46(11) 737-746, 2008 |
ABSTRACT
Mechanisms of sticking phenomena occurring during hot rolling of a modified STS 430J1L ferritic stainless steel have been investigated in this study by using a pilot-plant-scale rolling machine. As the rolling pass proceeds, the Fe-Cr oxide layer formed in a reheating furnace is destroyed, and the destroyed oxides penetrate into the rolled steel to form a thin oxide layer on the surface region. The sticking does not occur on the surface region containing oxides, whereas it occurs on the surface region without oxides by the separation of the rolled steel at high temperatures. This indicates that the resistance to sticking increases by the increase in the surface hardness when a considerable amount of oxides are formed on the surface region, and that the sticking can be evaluated by the volume fraction and distribution of oxides formed on the surface region. The lubrication and the increase of the rolling speed and rolling temperature beneficially affect to the resistance to sticking because they accelerate the formation of oxides on the steel surface region. In order to prevent or minimize the sticking, thus, it is suggested to increase the thickness of the oxide layer formed in the reheating furnace and to homogeneously distribute oxides along the surface region by controlling the hot-rolling process.
keyword : ferritic stainless steel, sticking, hot rolling, oxide
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The Effect of Various Electrolyte Concentrations on Surface and Electrical Characteristic of the Copper Deposition Layer at Anodizing of Titanium Anode
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이만형 Man Hyung Lee , 박은광 Eun Kwang Park , 우태규 Tae Gyu Woo , 박일송 Il Song Park , 윤영민 Young Min Yoon , 설경원 Kyeong Won Seol |
KJMM 46(11) 747-754, 2008 |
ABSTRACT
Recently, the requirement for the ultra thin copper foil increases with smaller and miniaturized electronic components. Therefore, it is important to examine the surface state of substrate depending on the processing parameter during the anodic oxidation. This study investigated the effect of the various electrolyte concentrations on anodizing of titanium anode prior to copper electrodeposition. Different surface morphology of anodized titanium was obtained at different electrolytic concentration 0.5 M to 3.0 M. In addition, the effect that the surfaces and the electrical characteristics on the electrodeposited copper layer was observed. In this study, surface anodized in the group containing 0.5M H2SO4 shows more uniform copper crystals with low surface roughness. the surface roughness and sheet resistance for 0.5M H2SO4 group were 1.353 μm and 0.104 mΩ/sq, respectively.
keyword : electrodeposition, anodic oxidation, sheet resistance, spark discharge
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IR Absorption Property in Nano-thick Ir-inserted Nickel Silicides
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윤기정 Ki Jeong Yoon , 송오성 Oh Sung Song , 한정조 Jeung Jo Han |
KJMM 46(11) 755-761, 2008 |
ABSTRACT
We fabricated thermally evaporated 10 nm-Ni/1 nm-Ir/(poly)Si films to investigate the energy saving property of silicides formed by rapid thermal annealing (RTA) at the temperature range of 300~1,200℃ for 40 seconds. Moreover, we fabricated 100 nm-thick ITO/(poly)Si films with an rf-sputter as references. A transmission electron microscope (TEM) and an X-ray diffractometer were used to determine cross-sectional microstructure and phase changes. A UV-VIS-NIR and FT-IR (Fourier transform infrared spectroscopy) were employed for near-IR and middle-IR absorbance. Through TEM analysis, we confirmed 20~65 nm-thick silicide layers formed on the single and polycrystalline silicon substrates. Ir-inserted nickel silicide on single crystalline substrate showed almost the same absorbance in near IR region as well as ITO, but Ir-inserted nickel silicide on polycrystalline substrate, which had the uniform absorbance in specific region, showed better absorbance in near IR region than ITO. The Ir-inserted nickel silicide on polycrystalline substrate particularly showed better absorbance in middle IR region than ITO. The results imply that nano-thick Ir-inserted nickel silicides may have excellent absorbing capacity in near-IR and middle-IR region.
keyword : Ir-inserted nickel silicide, infrared rays, absorbance, silicide
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Property of Nickel Silicides with Hydrogenated Amorphous Silicon Thickness Prepared by Low Temperature Process
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김종률 Jong Ryul Kim , 최용윤 Young Youn Choi , 박종성 Jong Sung Park , 송오성 Oh Sung Song |
KJMM 46(11) 762-769, 2008 |
ABSTRACT
Hydrogenated amorphous silicon(a-Si : H) layers, 120 nm and 50 nm in thickness, were deposited on 200 nm SiO2/single-Si substrates by inductively coupled plasma chemical vapor deposition(ICP-CVD). Subsequently, 30 nm-Ni layers were deposited by E-beam evaporation. Finally, 30 nm-Ni/120 nm a-Si:H/200 nm-SiO2/single-Si and 30 nm-Ni/50 nm a-Si:H/200 nm-SiO2/single-Si were prepared. The prepared samples were annealed by rapid thermal annealing(RTA) from 200℃ to 500℃ in 50℃ increments for 30 minute. A four-point tester, high resolution X-ray diffraction(HRXRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and scanning probe microscopy(SPM) were used to examine the sheet resistance, phase transformation, in-plane microstructure, cross-sectional microstructure, and surface roughness, respectively. The nickel silicide on the 120 nm a-Si:H substrate showed high sheet resistance(470 Ω/□) at T(temperature) < 450℃ and low sheet resistance (70 Ω/□) at T > 450℃. The high and low resistive regions contained ζ-Ni2Si and NiSi, respectively. In case of microstructure showed mixed phase of nickel silicide and a-Si:H on the residual a-Si:H layer at T < 450℃ but no mixed phase and a residual a-Si:H layer at T > 450℃. The surface roughness matched the phase transformation according to the silicidation temperature. The nickel silicide on the 50 nm a-Si:H substrate had high sheet resistance(~1 kΩ/□) at T < 400℃ and low sheet resistance (100 Ω/□) at T > 400℃. This was attributed to the formation of δ-Ni2Si at T > 400℃ regardless of the siliciation temperature. An examination of the microstructure showed a region of nickel silicide at T < 400℃ that consisted of a mixed phase of nickel silicide and a-Si:H without a residual a-Si:H layer. The region at T > 400℃ showed crystalline nickel silicide without a mixed phase. The surface roughness remained constant regardless of the silicidation temperature. Our results suggest that a 50 nm a-Si:H nickel silicide layer is advantageous of the active layer of a thin film transistor(TFT) when applying a nano-thick layer with a constant sheet resistance, surface roughness, and δ-Ni2Si temperatures > 400℃.
keyword : nickel silicide, ICP-CVD, hydrogenated amorphous silicon, nano-thick process, RTA
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