• 한국분말재료학회지
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• 제22권4호
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• pp.266-270
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• 2015

The synthesis of NiTi alloy powders by hydrogen reduction and dehydrogenation process of NiO and $TiH_2$ powder mixtures is investigated. Mixtures of NiO and $TiH_2$ powders are prepared by simple mixing for 1 h or ball milling for 24 h. Simple-mixed mixture shows that fine NiO particles are homogeneously coated on the surface of $TiH_2$ powders, whereas ball milled one exhibits the morphology with mixing of fine NiO and $TiH_2$ particles. Thermogravimetric analysis in hydrogen atmosphere reveals that the NiO and $TiH_2$ phase are changed to metallic Ni and Ti in the temperature range of 260 to $290^{\circ}C$ and 553 to $639^{\circ}C$, respectively. In the simple-mixed powders by heat-up to $700^{\circ}C$, agglomerates with solid particles and solidified liquid phase are observed, and the size of agglomerates is increased at $1000^{\circ}C$. From the XRD analysis, the presence of liquid phase is explained by the formation and melting of $NiTi_2$ inter-metallic compound due to an exothermic reaction between Ni and Ti. The simple-mixed powders, heated to $1000^{\circ}C$, lead to the formation of NiTi phase but additional Ni-, Ti-rich and Ti-oxide phases. In contrast, the microstructure of ball-milled powders is characterized by the neck-grown particles, forming $Ni_3Ti$, Ti-oxide and unreacted Ni phase.

• 대한화학회지
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• 제36권4호
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• pp.546-551
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• 1992

니켈(Ⅱ)이온을 N-benzylisonitrosoacetylacetone imine(HIAANB)으로 용매추출할 때의 반응메카니즘을 분광광도법으로 연구하였다. 유기상 chloroform에 녹아있는 리간드 HIAANB농도와 수용액층의 pH값을 변화시켜 가면서 흡광도를 측정하였다. 측정 데이터로부터 반응속도가 HIAANB농도에 대하여는 1차, [$H^+$]에 대하여는 -1차임을 알 수 있었다. 추출반응의 속도결정단계와 속도식은 다음과 같다. $Ni^{2+}$＋HIAANB ${\to}$ Ni-IAANB$^+$＋$H^+$ -d[Ni$^{2+}$] / dt = K'[Ni$^{2+}$][HIAANB]$_0$ / [H$^+$]. 수용액 중의 니켈(Ⅱ)이온을 분광광도법으로 정량할 때의 검정곡선은 최적실험조건에서 1.17ppm 이하의 농도범위에서 직선이었다. 또 리간드 대 금속의 결합비, 추출율과 수용액상의 pH 사이의 관계, 니켈(Ⅱ)이온을 정량할 때의 방해이온의 영향도 조사하였다.

• 한국운동역학회지
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• 제16권4호
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• pp.83-94
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• 2006

The purpose of this study is to elucidate how walking speed influences on change of angles of lower extremity and ground reaction force in normal and obese people. One group with normal body weight who were experimented at a standard speed of 1.5m/s and the other obese group were experimented at two different walking speeds (standard speed of 1.5m/s and self-selected speed of 1.3m/s). We calculated angles of lower extremity and ground reaction force during stance phase through video recording and platform force measuring. When the obese group walked at the standard speed, dorsi-flexion angle of ankle got bigger and plantar-flexion angle of ankle got smaller, which were not statistically significant. There was no significant difference of knee joint angles between normal and obese group at the same speed walking but significant post hoc only for the first flexion of knee joint in obese group. $F_z1$ was bigger than $F_z3$ in vertical axis for ground reaction force in both groups at the standard speed walking and the same force value at self-selected speed in obese group. $F_y3$ was always bigger than $F_y1$ in anterior-posterior axis in both groups.

• 한국수소및신에너지학회논문집
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• 제1권1호
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• pp.1-8
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• 1989

The hydriding kinetic mechanism and the change of the hydriding reaction rate of $MmNi_{4.5}Al_{0.5}$ during the thermally induced hydrogen absorption-desorption cycling are investigated. Comparison of the reaction rate data which are obtained by the pressure sweep method with the theoretical rate equations suggests that the hydriding rate controlling step has changed from the dissociative chemisorption of hydrogen molecules at the surface to the hydrogen diffusion through the hydride phase with the increase of the hydriding fraction. These hydriding kinetic mechanism is not changed during the cycling. However, the intrinsic hydriding reaction rate of $MmNi_{4.5}Al_{0.5}$ after 5500 cycles increases significantly comparing with the activated one. It is suggested that the change of the hydriding kinetic behavior due to intrinsic degradation of $MmNi_{4.5}Al_{0.5}$ can be interpreted as follows ; the formation of nickel cluster at the surface of the sample and the host metal atom exchange in bulk by thermal cycling.

• 한국결정성장학회지
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• 제7권3호
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• pp.494-503
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• 1997

Polyimide(PI)위에서 Cu의 초기 성장과정을 설명하기 위해, PI 위에 Cu를 조금씩 증착시키면서 그리고 PI 위에 Cu 층을 쌓아놓고 이 Cu 층을 $Ar^+$ 이온으로 깍아내면서 계면에서의 변화를 XPS를 이용하여 비교ㆍ관측하였다. 상온에서 PI위에 Cu를 조금씩 증착하면서 관측하였을 때, 그 성장과정에 따르는 phase의 변화는 Cu-N-O complex에서 $Cu_2O$ phase로, 그리고 metallic Cu 순으로 성장하는 것이 관측되었다. 반면에 PI위에 증착되어 있는 Cu를 조금씩 깎아내면서 관측하였을 때, metallic Cu가 $Ar^+$ 이온으로 깍아내어 polyimide와의 계면에 도달하게 되었을 때에는 Cu$_2$O phase로서 관측되었다. 이상의 결과로부터, in-situ로 Cu를 조금씩 올리면서 계면을 조사하는 것과 Cu를 증착시킨 후, 깍으면서 계면을 조사하는 것과는 다른 결과를 얻게 된다는 것을 알 수 있었다.

• 대한용접접합학회:학술대회논문집
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• 대한용접접합학회 2005년도 추계학술발표대회 개요집
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• pp.262-264
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• 2005

$Bi_{2}Sr_{2}CaCu_{2}O_{x}$(Bi-2212) and $Bi_{2}Sr_{2}Ca_{2}Cu_{3}O_{y}$(Bi-2223) high-$T_{c}$ superconductor(HTS) coating have been prepared by plasma spraying and heaat treatment. The Bi-2212 HTS coating later is synthesized through the peritectic reaction between Sr-Ca-Cu oxide coating layer and Bi-Cu oxide coating later, and $Bi_{2}Sr_{2}CaCu_{2}O_{y}$(Bi-2212) superconducting phase grow by partial melting process. The superconducting characteristic depends strongly on the conditions of the partial melting process. the Bi-2212 HTS layer consists of the whiskers grown in the diffusion direction. Above the 2212 layer, Bi-2223 phase and secondary phase was observed. The secondary phase is distributed uniformly over the whole surface. This is caused to the microcrack on the coatings surface. Despite everything, the film shows superconducting with an onset $T_{c}$ of about 115K. There are two changes steps. One changes (1step) at 115K is due to the diamagnetism of the Bi-2223 phase and the other changes (2step) at 78K is due to the diamagnetism of the Bi-2212 phase.

• 대한화학회지
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• 제54권4호
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• pp.437-442
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• 2010

수용액 속에서 $NaHSO_4$, TBAB (phase transfer catalyst), ionic liquid (IL) (1-butyl-3-methyl imidazolium hydrogen sulphate [bmim]$HSO_4$)를 사용하여, formalin, ${\beta}$-naphthol, aromatic amines을 반응시켜서 대응하는 2,3-dihydro-2-phenyl-1Hnaphtho-[1,2-e] [1,3] oxazine 유도체를 합성할 수 있는 보다 친환경적이고, 수율이 좋고, 크로마토그래피 분리 방법을 사용하지 않는 합성 방법을 개발하였다.

• Bulletin of the Korean Chemical Society
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• 제30권6호
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• pp.1325-1330
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• 2009

A general method has been developed for the solid phase synthesis of drug-like 7-aryl-benzo[b][1,4]oxazin-3(4H)- one derivatives 6. The method relies on a novel, microwave irradiation promoted cyclization reaction of the BOMBA resin bound, N-substituted-$\alpha$-(2-chloro-4-bromophenoxy)acetamide 3 that takes place via a Smiles rearrangement. The 7-bromobenzo[1,4]oxazine 4, produced in this process is converted to 7-aryloxazin analogs 5 by utilizing Suzuki coupling with various substituted arylboronic acids. Finally, the target 7-aryl-benzo[b][1,4]oxazin-3(4H)-ones 6 are liberated from the resin by treatment with 5% TFA. The progress of the reactions involved in this preparative route can be monitored by using ATR-FTIR spectroscopy on a single bead. The target compounds, obtained by using this five-step sequence, are produced in high yields and purities.

• 한국항공우주학회지
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• 제37권1호
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• pp.82-88
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• 2009

정상파 시스템의 구조는 발열반응으로 상변화를 하는 물질의 연속방정식에 의해 타당성을 검증받는다. 1차원 연속체 충격 구조 분석에서의 이론적 배경을 기반으로, 상변화 현상과 관련된 파의 마이크로 두께를 산출하였다. 상변화를 하는 물질로써, n-heptane은 탄화수소 연료의 증발과 응축 분석에 사용하였고, HMX은 고체 로켓 연료의 용융과 응고 분석에 사용하였다. n-heptane의 증발-응축 면의 산출 두께는 $10^{-2}$ 마이크론 차수이고, 반면에 HMX의 용융-응고 면의 산출 두께는 1 마이크론 차수 이다. 소개된 상면 두께 산출 이론은 실험적으로 얻을 수 없는 방대한 범위의 에너지 물질까지 계산범위를 확장시킬 수 있다.

• The Korean Journal of Ceramics
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• 제6권1호
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• pp.78-82
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• 2000

Although alumina aggregates have been used as refractory aggregates due to the improved mechanical properties of refractories as a result of the low contraction of alumina aggregates, the aggregates have a difficulty in fabrication due to its low sinterability. Two types of alumina aggregates and a fused alumina aggregate containing transient liquid forming additives are prepared to investigate the sintering characteristics of aggregates. $Al_2O_3$rich composition in the $Al_2O_3$-MgO-$SiO_2$(-$TiO_2$) system is chosen for the transient liquid phase sintering and the final recrystallized bonding phase between grains inside the fused alumina aggregates is found to be a needle-like mullite phase. The flexural strength of alumina bars, reaction-bonded using the paste having a composition of $Al_2O_3$-MgO-$SiO_2$-$TiO_2$, is about 78 MPa, which is one half value of that of pure alumina.