• 한국재료학회지
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• 제9권7호
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• pp.688-694
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• 1999

Ti-6Al-4V 합금을 타겟트로 사용하여 유리 기판위에 dc reactive magnetron sputtering법으로 $N_2$/(Ar+N_2)$ 비, 기전력 및 시간등의 여러 가지 증착 조건에서 Ti-6Al-4V-N 필름을 증착하였고, 각각의 증착 조건에 따른 결정구조 및 우선방위 거동은 X-선 회절장치를 사용하여 조사하였다. Ti-6Al-4V-N 필름은 본질적으로 fcc 결정구조의 $\delta$-TiN에 Al과 V이 결함으로서 고용된 변형된 형태의 $\delta$-TiN구조이고, TiN의 격자상수(4.240 )보다 작은 값을 나타내었는데, 이는 Ti(1.47 )에 비하여 상대적으로 원자반경이 작은 Al(1.43 )과 V (1.32 )이 Ti의 격자위치에 치환된 결과이다. 그리고 Ti-6Al-4V-N 필름은 $_N2$가스 분압이 감소됨에 따라 (111) 우선방위 성장거동을 하였을 뿐만아니라 증착시간의 증가에 따라 뚜렷한 (111) 우선방위 성장거동을 나타내었다. 그리고 증착속도 및 결정입도의 거동 또한 여러 가지 증착 조건에 크게 의존한다

• Bulletin of the Korean Chemical Society
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• 제13권1호
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• pp.11-17
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• 1992

Vibration-to-vibration energy transfer probabilities for $HF(v=n)+H_2(v=0){\to}HF(v=n-1)+H_2(v=1)$ and $DF(v=n)+D_2(v=0){\to}DF(v=n-1)+D_2(v=1)$ including both the vibration-to-vibration and translation (V-V, T) and vibration-to-vibration and rotation (V-V, R) energy transfer paths have been calculated semiclassically using a simplified collision model and Morse-type intermolecular interaction potential. The calculated results are in reasonably good agreement with those obtained by experimental studies. They also show that the transition processes for $HF(v=1-3)+H_2(v=0){\to}HF(v=0-2)+H_2(v=1)$ and $DF(v=1,\;4)+D_2(v=0){\to}DF(v=0,\;3)+D_2(v=1)$ are strongly dependent on the V-V, T path at low temperature but occur predominantly via the V-V, R path with rising temperature. The vibration-to-vibration energy transfer for $HF(v=4)+H_2(v=0){\to}HF(v=3)+H_2(v=1)$ and $DF(v=2-3)+D_2(v=0){\to}DF(v=1-2)+D_2(v=1)$ occur predominantly via V-V, R path and V-V, T path through whole temperatures, respectively.

• 한국재료학회지
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• 제29권9호
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• pp.519-524
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• 2019

Spherical $Li_3V_2(PO_4)_3$ (LVP) and carbon-coated LVP with a monoclinic phase for the cathode materials are synthesized by a hydrothermal method using $N_2H_4$ as the reducing agent and saccharose as the carbon source. The results show that single phase monoclinic LVP without impurity phases such as $LiV(P_2O_7)$, $Li(VO)(PO_4)$ and $Li_3(PO_4)$ can be obtained after calcination at $800^{\circ}C$ for 4 h. SEM and TEM images show that the particle sizes are $0.5{\sim}2{\mu}m$ and the thickness of the amorphous carbon layer is approximately 3~4 nm. CV curves for the test cell are recorded in the potential ranges of 3.0~4.3 V and 3.0~4.8 V at a scan rate of $0.01mV\;s^{-1}$ and at room temperature. At potentials between 3.0 and 4.8 V, the third $Li^+$ ions from the carbon-coated LVP can be completely extracted, at voltages close to 4.51 V. The carbon-coated LVP exhibits an initial specific discharge capacity of $118mAh\;g^{-1}$ in the voltage region of 3.0 to 4.3 V at a current rate of 0.2 C. The results indicate that the reducing agent and carbon source can affect the crystal structure and electrochemical properties of the cathode materials.

• 한국표면공학회지
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• 제34권2호
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• pp.135-141
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• 2001

Arc-melted Ti-6Al-4V, Ti-4Fe and Ti-(1,2) Si alloys were oxidized at 700, 800, 900 and $1000^{\circ}C$ in air. The oxidation resistance of Ti-4Fe was comparable to that of Ti-6Al-4V, while the oxidation resistance of Ti-(1,2) Si was superior to that of Ti-6Al-4V. Ti-2Si displayed the best oxidation resistance among the four alloys, but failed after oxidation at $1000^{\circ}C$ for 17h. The oxide scale formed on Ti-6Al-4V, Ti-4Fe and Ti-(1,2)Si consisted of ($TiO_2$ and a small amount of $Al_2$$O_3$), ($TiO_2$ and a small amount of dissolved iron), and ($TiO_2$ plus a small concentration of amorphous $SiO_2$), respectively. The oxide grains of the surface scale of the four alloys were generally fine and round.

• 대한화학회지
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• 제18권4호
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• pp.259-266
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• 1974

과염소산 수용액 중에서 바나듐(III)이온이 산소에 의해 산화되는 반응에 대해서 pH 범위1∼3에 걸쳐 $H_2O^{18}$을 이용한 동위원소 실험을 행했다. 반응속도식$-\frac{d[V(III)]}{dt}=k_1\frac{[O_2][V(III)]}{[H^+]}$가 성립되는 높은 히드로늄이온 농도(pH<∼2)에서는 반응생성물 $VO^{2+}$이온의 산소가 모두 산소분자에서 유래된다는 결과를 얻었다. 반면 $-\frac{d[V(III)]}{dt}=K_2\frac{[O_2][V(III)]^2}{[Ht]^2}$의 속도식이 성립하는 pH>∼2 범위에서의 추적자 실험은 바나딜이온의 산소의 50%가 산소분자에서 온다는 결과를 주었다. 반응속도론의 결과 화학량론적 결정과 아울러 동위원소 실험결과를 고려하면 다음과 같은 반응 메카니즘을 제안할 수 있다.$$V^{3+}\rightleftarrows VOH^{2+} + H+, 2VOH^{2+}\rightleftarrowsV_2(OH)_2^{4+}$$$$ 낮은\PH:\ VOH^{2+}+O_2 \rightarrow V(O_2)OH^{2+}, V(O_2)OH^{2+}+VOH^{2+}\rightarrow 2VO^{2+}+H_2O_2$$$$ 높은\PH:\V2(OH)_2^{4+}+O_2\rightarrow2VO^{2+}+H_2O_2, V_2(OH)_2^{4+}+H_2O_2\rightarrow2VO^{2+}+2H_2O$$

• 한국분말재료학회지
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• 제29권1호
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• pp.8-13
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• 2022

In this study, we have prepared a Ti-6Al-4V/V/17-4 PH composite structure via a direct energy deposition process, and analyzed the interfaces using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The joint interfaces comprise two zones, one being a mixed zone in which V and 17-4PH are partially mixed and another being a fusion zone in the 17-4PH region which consists of Fe+FeV. It is observed that the power of the laser used in the deposition process affects the thickness of the mixed zone. When a 210 W laser is used, the thickness of the mixed zone is wider than that obtained using a 150 W laser, and the interface resembles a serrated shape. Moreover, irrespective of the laser power used, the expected σ phase is found to be absent in the V/17-4 PH stainless steel joint; however, many VN precipitates are observed.

• 충청수학회지
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• 제27권4호
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• pp.603-614
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• 2014

We introduce the concepts of ($\mathcal{T}^{{\mu}{\gamma}}$, $\mathcal{U}^{{\mu}{\gamma}}$)-double (r, s) (u, v)-semiclosures and ($\mathcal{T}^{{\mu}{\gamma}}$, $\mathcal{U}^{{\mu}{\gamma}}$)-double (r, s)(u, v)-semiinteriors. Using the notions, we investigate some of characteristic properties of double pairwise (r, s)(u, v)-semicontinuous, double pairwise (r, s)(u, v)-semiopen and double pairwise (r, s)(u, v)-semiclosed mappings.

• Molecules and Cells
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• 제39권4호
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• pp.322-329
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• 2016

Voltage-gated $Ca^{2+}$ ($Ca_V$) channels are dynamically modulated by Gprotein-coupled receptors (GPCR). The $M_1$ muscarinic receptor stimulation is known to enhance $Ca_V2.3$ channel gating through the activation of protein kinase C (PKC). Here, we found that $M_1$ receptors also inhibit $Ca_V2.3$ currents when the channels are fully activated by PKC. In whole-cell configuration, the application of phorbol 12-myristate 13-acetate (PMA), a PKC activator, potentiated $Ca_V2.3$ currents by ~two-fold. After the PMA-induced potentiation, stimulation of $M_1$ receptors decreased the $Ca_V2.3$ currents by $52{\pm}8%$. We examined whether the depletion of phosphatidylinositol 4,5-bisphosphate ($PI(4,5)P_2$) is responsible for the muscarinic suppression of $Ca_V2.3$ currents by using two methods: the Danio rerio voltage-sensing phosphatase (Dr-VSP) system and the rapamycin-induced translocatable pseudojanin (PJ) system. First, dephosphorylation of $PI(4,5)P_2$ to phosphatidylinositol 4-phosphate (PI(4)P) by Dr-VSP significantly suppressed $Ca_V2.3$ currents, by $53{\pm}3%$. Next, dephosphorylation of both PI(4)P and $PI(4,5)P_2$ to PI by PJ translocation further decreased the current by up to $66{\pm}3%$. The results suggest that $Ca_V2.3$ currents are modulated by the $M_1$ receptor in a dual mode-that is, potentiation through the activation of PKC and suppression by the depletion of membrane $PI(4,5)P_2$. Our results also suggest that there is rapid turnover between PI(4)P and $PI(4,5)P_2$ in the plasma membrane.

• 전자공학회논문지A
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• 제31A권10호
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• pp.71-78
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• 1994

We have developed GaAs power metal semiconductor field effect transistors (MESFETs) for 4.7V operation under 900 MHz using a low-high deped structures grown by molecular beam epitaxy (MBE). The fabricted MESFETs with a gate widty of 7.5 mm and a gate length of 1.0.mu.m show a saturated drain current (Idss) of 1.7A and an uniform transconductance (Gm) of around 600mS, for gate bias ranged from -2.4 V to 0.5 V. The gate-drain breakdown voltage is measured to be higher than 25 V. The measured rf characteristics of the MESFETs at a frequency of 900 MHz are the output power of 31.4 dBm and the power added efficiency of 63% at a drain bias of 4.7 V.

• 공업화학
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• 제7권2호
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• pp.362-370
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• 1996

$Li/V_6O_{13}$ 전지의 성능과 poly(acrylonitrile)[PAN]계 폴리머 전해질의 전기화학적인 성질을 조사 하였다. 폴리머 전해질의 이온 전도도는 상온에서 $2.3{\times}10^{-3}S/cm$를 보였으며 리튬 전극과의 상용성도 우수하였다. 또한 4.3V(vs. $Li^+/Li$)까지의 전기화학적인 안정성이 있는 것으로 나타났다. $Li/V_6O_{13}$ 전지 반응은 $V_6O_{13}$ 전극과 폴리머 전해질간의 계면 저항이 지배적 이었다. $V_6O_{13}$내의 리튬 이온의 확산 계수값은 $2.7{\times}10^{-9}{\sim}4.2{\times}10^{-8}cm^2/sec$로 나타났다. $V_6O_{13}$ 활물질의 이용률은 C/8($50{\mu}A/cm^2$)에서 95%였으며 C/4($100{\mu}A/cm^2$)에서는 82%로 각각 나타났다.