• 한국결정성장학회지
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• 제5권1호
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• pp.60-66
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• 1995

초음파 분무기에 의해 분무된 질산아연 염($Zn(NO_3)_2$) 용액(0.5M)의 에어로졸 거동과 분포에 대한 실제 실험 결과는 computer simulation 결과와 일치하였다. 즉, 반응관(thermophoresis)에 의해 반응관 중심부로 이동하였다. 또한 에어로졸의 농도 분포는 축길이가 증가함에 따라 반응관 중심쪽에 높았다. 합성된 ZnO 입자 중에서 반응과 중심에서는 볼 수 없었던 깨진 형태의 shell-like aggregates가 반응관 벽근처에서 관찰되었으며, 입자의 크기는 반응관 벽쪽($ 1.2 {\mu\textrm{m}$)이 중심쪽($0.9 {\mu\textrm{m}$)보다 컸다.

• 한국결정성장학회지
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• 제24권5호
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• pp.219-223
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• 2014

Pulsed laser ablation in liquid medium was successfully employed to synthesize hydroxyapatite colloidal nanoparticles. The crystalline phase, particle morphology, size distribution and microstructure of the hydroxyapatite nanoparticles were investigated in detail. The obtained hydroxyapatite nanoparticles had spherical shape with sizes ranging from 5 to 20 nm. The laser ablation and the nanoparticle forming process were discussed with explosive ejection mechanism by investigating change of surface morphology on target. The analytical results of XPS, FT-IR and Raman spectroscopy confirms that the stoichiometry and bonding properties of the hydroxyapatite nanoparticles are in good agreement with reported bulk hydroxyapatite materials.

• 한국초전도저온공학회:학술대회논문집
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• 한국초전도저온공학회 2003년도 추계학술대회 논문집
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• pp.93-95
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• 2003

YBa$_2$Cu$_3$O$_{x}$ (Y123) single crystal was grown by TSMG (top seeded melt growth) method. Physical properties of Y123 single crystal were dependent on the shape and distribution of Y2BaCuOx (Y211) in it and on the oxygenation temperature and the holding time. In this work, It was investigated to an optimal oxygenation condition and a dependence of melting temperature and holding time on physical properties. The optimal oxygenation condition was found that it was heat-treated for 30 hours at 45$0^{\circ}C$, Also it was found that the critical current density and the size of Y211 were increased with the melting temperature and the holding time.e.

• 대한치과보철학회지
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• 제36권5호
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• pp.772-785
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• 1998

This study was undertaken to clarify the microstructure of the different IPS Empress ingots by etching and to observe the change of leucite crystal structure according to subsequent heat treatment and the crystal distribution according to sprue types(${\phi}2.8mm$, single sprue; ${\phi}1.8mm$, double sprue) by scanning electron microscopy. IPS Empress T1, O1 ingots used for staining technique, and Dentin(A2) ingots used for layering technique were selected for this study. To observe the microstructures of these ingots before pressing, the specimens were prepared in splinters($3{\times}3{\times}3mm$) taken from the original ingots. And to estimate crystal distribution and microstructural change by sprue type and subsequent heat treatment. the specimens($3{\times}3{\times}3mm$) were heat-pressed through the two types of sprues with different diameters and numbers, and all specimens were fired according to the recommended firing schedule. The observed surface was ground with waterproof papers($#800{\sim}#1800$) on the grind polisher and was cleaned ultrasonically. All specimen were etched with 0.5% hydrofluoric acid. After etching, the surface was treated by ion sputter coating for SEM observation at an accelerating voltage of 20kV. In all specimens, the central area of ground surface was observed because there was less difference in microstructure between the peripheral area and the central area. The results were as follows ; 1. In the microstructure according to the ingot type, there was a wide difference between the staining (T1,O1) and layering(Dentin A2) ingots, but there was not a considerable difference between the T1 ingot and the O1 ingot for staining technique. 2. In all specimens, the crystal dispersion of IPS Empress ceramic using double sprue was significantly more scattered than that of IPS Empress ceramic using single sprue. The degree of scattering was strongest in the Dentin(A2) specimen and weakest in the O1 ingot. 3. In the microstructural change according to the subsequent heat treatment, all of ingots had some microcracks in the inside of the leucite crystal and the glass matrix after pressing. The inner splinters of the leucite crystal became smaller, and more microcracks occurred in the glass matrix due to increasing heat treatment times. 4. The size of leucite crystals varied from $1{\mu}m\;to\;5{\mu}m$. The mean size of mature crystals was about $5{\mu}m$. The form of the crystal was similar to a circle when it was smaller and similar to an ellipse when it was larger.

• 한국결정성장학회지
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• 제30권4호
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• pp.123-130
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• 2020

AGM 연축전지(Absorbent Glass Mat Lead-Acid Battery)의 수명 특성을 결정짓는 양극 활물질(Active Material)의 주요 구성 결정인 4BS(Tetrabasic lead Sulfate)의 입자 크기를 제어하기 위해 4BS Nano Seed(NS)를 적용 중에 있다. 4BS NS 적용 시, 나노 입자 특성상 분산 안정성이 저하되어 제 기능을 다하지 못한다. 이를 개선하기 위해 기존 첨가제인 광명단(Red Lead)에 나노 입자의 4BS seed가 포함된 Incorporated Nano Seed(INS)를 함량별로 첨가하여 양극판 분석과 제품 성능을 평가하였다. INS 함량이 증가할수록 4BS 입자 크기는 작아지면서 균일해지는 특성을 확인할 수 있었으며, 반응 비표면적 증가에 따른 고율 방전 특성도 향상되는 것을 알 수 있었다. 극판 제조 공정에서의 개별 극판에 대한 입도 분포의 편차를 확인하기 위해, AGM 연축전지 200 대 대한 내부 저항 및 전압 검사를 진행하였으며 제품 제조 공정 품질 편차가 감소하는 것을 확인하였다.

• 한국결정성장학회지
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• 제12권5호
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• pp.229-233
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• 2002

유기화학적 방법인 착체중합법을 이용하여 나노사이즈의 ZnO 분말을 저온에서 합성하였다. 고분자 전구체는 Zn nitrate hexahydrate를 사용하였고, chelating agent로서 citric acid를 reaction medium으로서 ethylene glycol을 혼합하여 제조하였다. 고분자 전구체를 300~$700^{\circ}C$의 온도범위에서 3시간 동안 하소하였으며, 열분해와 결정화 과정을 TG-DTA, FI-IR과 XRD 등을 이용하여 분석하였다. 결정화 온도에 따른 입자의 형상이나 크기를 SEM, TEM의 분석 및 Scherrer's equation을 이용한 계산을 통하여 관찰 및 비교를 하였다. ZnO의 결정화는 $300^{\circ}C$부터 시작되었고, $400^{\circ}C$에서 완전히 합성되었음을 알 수 있었다. 400~$700^{\circ}C$에서 하소된 ZnO 입자들은 대부분 둥근 형태로 균일하게 분포되었으며, $400^{\circ}C$에서 하소된 분말의 평균입도는 약 30~40nm를 보였다. 일반적으로 온도의 상승에 따라 입경이 증가되는 일반적인 경향이 관찰되었다.

• 한국결정성장학회지
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• 제7권1호
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• pp.47-58
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• 1997

본 연구에서는 수열성장법을 이용해서 알루미늄 수화물인 깁사이트로부터 코런덤($\alpha$-$Al_2O_3$) 단결정 분말을 제조하였으며, 주요 반응인자로서 광화제와 성장기질의 특성이 생성물의 입도분포와 결정성에 미치는 영향을 조사했다. 실험결과 성장용액의 용해도를 증가시키기 위해 광화제로 사용된 KOH의 첨가량이 증가할수록 코런덤 입자의 크기가 커졌고, 수열반응 온도는 낮아졌으나, 영양제인 깁사이트의 농도가 증가할수록 합성된 코런덤 입자는 작아졌다. 성장기질의 물성특성 차이에 따라 수열합성 조건이 달라졌다. 수열합성을 통해 400~$470^{\circ}C$인 반응온도 범위에서 1~10 $\mu \t extrm{m}$ 정도의 중량평균 입경을 갖는 육방정의 코런덤 결정을 합성하였다.

• 한국재료학회지
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• 제33권9호
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• pp.360-366
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• 2023

This study focuses on how the partial substitution of copper by nickel nanoparticles affects the electrical and structural properties of the Bi₂Ba₂Ca₂Cu_2.9Ni_0.1O_10+δ, Bi₂Ba₂Ca₂Cu_2.8Ni_0.2O_10+δ and Bi₂Ba₂Ca₂Cu_2.6Ni_0.4O_10+δ compounds. Approximate values of crystallization size and crystallization percentage for the three compounds were calculated using the Scherer, modified Scherer, and Williamson-Hall methods. A great similarity was observed in the crystal size values from the Scherer method, 243.442 nm, and the Williamson-Hall method, 243.794 nm for the second sample. At the same time this sample exhibited the highest crystal size value for the three methods. In the examination of electrical properties, the sample with 0.1 partial substitution, Bi₂Ba₂Ca₂Cu_2.9Ni_0.1O_10+δ was determined to be the best with a critical temperature of 100 K and an energy gap of 6.57639 × 10^-21 MeV. Using the SEM technique to analyze the structural morphology of the three phases, it was discovered that the size of the granular forms exceeds 25 nm. It was determined that the samples' shapes alter when nickel concentration rises. The patterns that reveal the distribution of the crystal structure also exhibit clear homogeneity.

• 전기화학회지
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• 제13권1호
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• pp.40-44
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• 2010

In this work, highly uniform size-controlled $Cu_2O$ nanocubes can be successfully formed by means of pulse electrodeposition. The size distribution, crystal structure, and chemical state of deposited $Cu_2O$ nanocubes are characterized using scanning electron microscopy, transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. The phase transition from $Cu_2O$ to Cu can be controlled by constant current electrodeposition as a function of deposition time. In particular, the size of the $Cu_2O$ nanocubes can be controlled using pulse electrodeposition as a function of applied current density.

• 한국세라믹학회지
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• 제35권9호
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• pp.958-968
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• 1998

Porous silica ceramics were prepared using DCCA(Drying Control Chemical Additives) Such as uncharged polymer(Polyethylene glycol) and protein (Lipase) under H2O/Low-grade TEOS=10 C2H5OH/Low-grade TEOS=1 HC1/Low=grade TEOS=0.01 After Plain which doesn't added DCCA and samples of 11 sorts which varied molecular weight of PEG(Mw=600, 1000, 2000) quantity of Lipase and concentration of wat-er were synthesized gellation time and thermal analysis were investigated. After heat-treated at 600, cry-stal structures analyses of SiO2 polymer and characteristics of pores were investigated. Gellation time was retarded about 2-6 times as compared with plain resulting in addition of DCCA and crystal structures ex-hibited amorphous state. Moreover as increase of water a short gellation time was obtained. The samples added PEG showed increase of specific surface areas up to 20-40% and had micropores while those of Lipase were decreased about 90% and showed broad pore size distribution.