• 한국재료학회지
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• 제11권6호
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• pp.492-497
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• 2001

통계적 방법을 사용하여 스퍼터 증착한 Ta 박막의 증착속도, 비저항, 면저항 균일도, 반사도, 응력 등의 물성을 측정하고 분석하였다. RS/1의 표면 반응 분석법에 의해 독립변수와 종속변수간의 함수관계를 예측하였으며. 이때 비저항과 면저항의 균일도 측면에서 최적조건은 증착 압력 2 mTorr, 증착 전력 8 W/$\textrm{cm}^2$ 및 기판온도 $20^{\circ}C$였다. 실험 모텔의 신뢰성 (fitness)은 풀링(pooling)하지 않은 경우 0.85 ~0.9의 값을 얻었다. 본 조건하에서 증착된 박막은 비저항 180$\mu$$\Omega$cm와 면저항 균일도 ~ 2%의 값을 가졌다. 투과전자 현미경과 X선 회절법을 이용하여 분석한 결과 증착된 박막은 100~200 정도의 결정립 크기를 갖는 $\beta$-Ta 임을 확인하였다.

• 한국전기전자재료학회논문지
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• 제15권1호
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• pp.67-74
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• 2002

A phosphor for Plasma Display Panel, BaMgAl$_{10}$ O$_{17}$ :Eu$^{2+}$, showing a blue emission band at about 450nm was prepared by a solid-state reaction using BaCO$_3$, $Al_2$O$_3$, MgO, Eu$_2$O$_3$ as starting materials wish flux AlF$_3$. The study of the behaviour of Eu in BAM phosphor was carried out by the photoluminescence spectra and the Rietveld method with X-ray and neutron powder diffraction data to refine the structural parameters such as lattice constants, the valence state of Eu, the preferential site of Mg atom and the site fraction of each atom. The phenomenon of the concentration quenching was abound 2.25~2.3wt% of Eu due to a decrease in the critical distance for energy transfer of inter-atomic Eu. Through the combined Rietveld refinement, R-factor, R$_{wp}$, was 8.11%, and the occupancy of Eu and Mg was 0.0882 and 0.526 at critical concentration. The critical distance of Eu$^{2+}$ in BAM was 18.8$\AA$ at 2.25% Eu of the concentration quenching. Furthermore, c/a ratio was decreased to 3.0wt% and no more change was observed over that concentration. The maximum entropy electron density was found that the modeling of $\beta$-alumina structure in BaMgAl$_{10}$ O$_{17}$ :Eu$^{2+}$correct coincided showing Ba, Eu, O atoms of z= 1/4 mirror plane.e.ane.e.

• 한국결정성장학회지
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• 제20권5호
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• pp.237-242
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• 2010

Mg-BCP(Mg Substituted BCP)를 제조하기 위하여 $Ca(NO_3)_2{\cdot}4H_2O$(Katayama chemical, Japan)과 $(NH_4)_2{\cdot}HPO_4$ (Junsei chemical, Japan), $Mg(NO_3)_2{\cdot}6H_2O$(Junsei chemical, Japan)를 출발물질로 공침법(co-precipitation process)을 이용하여 합성하였다. 제조된 분말의 마그네슘의 첨가에 따른 분말의 분광학적 특성은 FT-IR(MAGNA-IR 560, Nicolet)을 통하여 분석하였으며, SEM(S-4200, Hitachi)을 통하여 미세구조를 분석하였다. XRD 회절피크의 면적적분강도를 Integral Analysis (Rigaku, Japan)를 이용하여 HAp와 ${\beta}$-TCP의 비율을 확인하였다. 1.0 wt% 마그네슘이 첨가된 BCP 샘플의 경우 Hank's solution에서의 2주 침적 후 표면에 침상의 HAp로 추정되는 결정이 성장하였다. 이러한 미세구조의 변화는 생활성을 가지는 마그네슘의 첨가가 BCP 조직 내에서 표면의 활성을 증가시켜 결정의 성장을 촉진시킨 것으로 판단된다.

• 전자공학회논문지
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• 제53권11호
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• pp.99-106
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• 2016

라돈이 기관지나 폐포에 머무르게 될 때 라돈의 붕괴로 인해 자핵종(알파선, 베타선, 감마선 등)들이 생성되면서 이것들이 방사선을 방출하는데 세포의 염색체에 돌연변이를 일으켜 폐암을 발생할 가능성이 존재한다. 다시 말해 폐암의 원인이 라돈가스 때문이라기보다는 흡수된 일부 라돈의 붕괴로 인해 생기는 부산물이 방사선을 방출하기 때문이라고 할 수 있다. 사람이 연간 노출되는 방사선의 82%가 자연방사선에 의한 것인데 그중 대부분이 라돈이다. 실내의 라돈 농도를 적절하게 제어할 수 있다면 폐암의 발생확률을 30%나 억제할 수 있다고 알려져 있다. 아직까지 실내의 라돈의 농도를 측정하는 데는 외국의 라돈 센서를 사용하고 있는 실정이다. 실내 라돈 방출량에 대한 데이터 구축과 국내에 맞는 실용적인 라돈측정기기를 개발하도록하는 연구가 필요하다. 본 논문에서는 PIN Photodiode를 이용하여 라돈의 농도를 측정하는 라돈 검출기 구현 방법을 제안한다. 실험을 통해서, PIN photodiode의 라돈 센서 모듈로서의 이용 가능성에 대하여 확인하였다.

• Journal of Pharmaceutical Investigation
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• 제35권4호
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• pp.279-285
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• 2005

Ground CS-891 (N-[1-(4-methoxyphenyl)-1-methylethyl]-3-oxo-4-aza-5a-androst-1-ene-$17{\beta}$-carboxamide) of poorly water soluble drug was obtained using a Heiko Seisakusho model TI-100 vibration mill, and samples with different crystallinity were prepared at mixture ratios of 10:0, 7:3, 5:5, 3:7 and 0:10 (intact;ground CS-891). Physicochemical characterizations were obtained using qualitative and quantitative X-ray diffractometry, different scanning calorimetry (DSC), scanning electron microscopy (SEM), Quantasorb surface area analyzer, and controlled atmosphere microbalance. With increase of amorphous CS-891 in mixture ratios, the intensities of X-ray diffraction peaks of crystalline CS-891 were decreased, whereas surface area, water absorption, and exothermic peaks in DSC were increased. The apparent solubility of ground CS-891 was $4.4\;{\mu}g/ml$ and the solubility of intact CS-891 was $3.1\;{\mu}g/ml$ at $37{\pm}1^{\circ}C$. The apparent precipitation rates of CS-891 in a supersaturated solution during the solubility test were increased with an increase of amorphous CS-891, and a crystalline form of CS-891 transformed from amorphous CS-891 after the solubility test was found by X-ray diffraction analysis, DSC and SEM. The dissolution profiles of CS-891 with different crystallinity at $37{\pm}1^{\circ}C$ by the USP paddle method were investigated, and the apparent dissolution rate constant of ground CS-891 was about 5.9-fold higher than that of intact CS-891. A linear relationships between the crystallinity of CS-891 and the apparent dissolution rate constant (r>0.96) were obtained.

• Applied Microscopy
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• 제46권1호
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• pp.27-31
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• 2016

It has been investigated what kind of characteristic X-ray in electron probe micro-analyzer (EPMA) is effective for the determination of compounds of Si series materials. After comparing the characteristic X-rays among the primary and secondary lines in $K_{\alpha}$ and $K_{\beta}$ obtained from the Si series standard samples, it was found that the secondary line of $K_{\alpha}$ exhibited the most informative spectrum although the intensity was considerably weak. As a result of analyzing the spectrum shapes of the Si series standard samples, the spectrum shape of the secondary line of $K_{\alpha}$ for SiC was different from those for other Si compounds. To grasp the characteristics of the shape, a line was perpendicularly drawn from the peak top to base line in order to divide a spectrum into two areas. The area ratio of right to left was defined to call as the asymmetry index here. As a result, the asymmetry index value of the SiC was greater than one, while those of other Si compounds were less than one. It was found from the EPMA analysis that identification of SiC became successful to distinguish from other Si compounds and this method was applicable for micro-sized compounds in a practical composite material.

• 한국세라믹학회지
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• 제22권3호
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• pp.53-59
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• 1985

Nucleation and crystallization of $\beta$-eucryptite in a glass of molecular percentage composition Li2O.Al2O3.2SiO2 are studied. The glasses are made by quenching of the melts from 143$0^{\circ}C$ to room temperature. Heat-treatment for nucleation and crystal growth are caried out at various temperature in the range between 50$0^{\circ}C$ and 80$0^{\circ}C$ with different duration of time. The amounts of crystallization are estimated by the method of x-ray powder diffraction. As the results a time-temperature-transformation relation for crystallization is derived. The maximum rate of crystallization is observed at about 75$0^{\circ}C$ from the T-T-T-curve while the crystallization temperature is detected at 67$0^{\circ}C$ by DTA measurement. The crystallization temperature moved to 62$0^{\circ}C$ by adding 5 weight percents of TiO2 and it moved to 78$0^{\circ}C$ by adding 2 weight percents of V2O5. The crystallization temperature moved to 62$0^{\circ}C$ by adding 5 weight percent of TiO2 it moved to 78$0^{\circ}C$ by adding 2 weight percents of V2O5 The activation energy for crystallization from the pure glass is calculated as 68 Kcal/mol and it varied to 53 Kcal/mol and 110Kcal/mol when 5 weight percents of TiO2 and weight percents of V2O5 are added respectively.

• Journal of Pharmaceutical Investigation
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• 제12권3호
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• pp.64-73
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• 1982

Molecular structures of ${\omega}-Amino$ acids, ${\omega}-Aminosulfonic$ acids and their ${\beta}-hydroxy$ substituted compounds were determined by X-ray diffraction method, and the similarities and differences between their molecular structures or between related compounds were discussed.

• 한국세라믹학회지
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• 제26권4호
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• pp.583-587
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• 1989

Various $\alpha$-silicon carbied and colloidal graphite particles were sintered at 155$0^{\circ}C$ in vacuum atmosphere by reaction bonding sintering method, and the physical properties and microstructural analysis of specimen were investigated. With decreasing particle size, sintered density and 3-point bending strength of materials were increased and 3.2${\mu}{\textrm}{m}$ specimen showed high density and strength, 3.05g/㎤, 40kg/$\textrm{mm}^2$, respectively. The results of X-ray diffractometer and optical micrographs analysis showed that graphite and silicon melt reacted to convert to fine $\beta$-SiC particle and the body was changed to dense material.

• Bulletin of the Korean Chemical Society
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• 제34권8호
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• pp.2367-2374
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• 2013

Lysine (Lys) immobilized on zeolite 4A was prepared by a simple adsorption method. The physical and chemical properties of Lys/zeolite 4A were investigated by X-ray diffraction (XRD), FT-IR, Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV-vis. The obtained organic-inorganic composite was effectively employed as a heterogeneous basic catalyst for synthesis of ${\alpha},{\beta}$-unsaturated carbonyl compounds. No by-product formation, high yields, short reaction times, mild reaction conditions, operational simplicity with reusability of the catalyst are the salient features of the present catalyst.