• 한국전기전자재료학회논문지
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• 제14권10호
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• pp.845-849
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• 2001

The new phto-alignment material PMI5CA, poly{N-(phenyl)maleimide-co-3-[4-(pentyloxy) cinamate]porpyl-2-hydroxy-1-methacrylate}, was synthesized and the electro-optical (EO)characteristics in the vertical-aligned(VA) liquid crystal display (LCD) photo-aligned on the photopolymer surface were studied. Excellent Voltage-transmittance(V-T) characteristics in the VA-LCD photoaligned with polarized UV exposure of oblique direction on the pohotopolymer surface for 1 min can be achieve. The transmittance of the VA-LCD photoaligned on the photopolymer surface decreased with increasing UV exposure time. We suggest that decrease of transmittance in the VA-LCD photoaligned on the photopolymer surface is attributed to the dissociation of the ester linkage in the photodimerized cinnamate structure with increasing UV exposure time.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2001년도 추계학술대회 논문집
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• pp.358-361
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• 2001

A new photoalignment material PM15CA, poly{N-(phenyl)maleimide-co-3-[4-(pentyloxy) cinnamate]propyl-2-hydroxy-1-methacrylate}, was synthesized and the electro-optical (EO) characteristics in the vertical-aligned (VA) liquid crystal display (LCD) photo-aligned on the photopolymer surface were studied. Excellent voltage-transmittance(V-T) characteristics in the VA-LCD photoaligned with polarized UV exposure of oblique direction on the pohotopolymer surfaces for 1 min can be achieved. The transmittance of the VA-LCD photoaligned on the photopolymer surface decreased with increasing UV exposure time. We suggest that the decrease of transmittance in the VA-LCD photoaligned on the photopolymer surface is attributed to the dissociation of the ester linkage in the photodimerized cinnamate structure with increasing UV exposure time

• 한국전기전자재료학회논문지
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• 제27권12호
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• pp.797-802
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• 2014

In this study, in order to develop the capacitor composition ceramics with the good dielectric properties, $(Ba_{1-x}Ca_x)(Ti_{0.85}Zr_{0.12}Sn_{0.03})O_3$ (abbreviated as BCTZ) ceramics were prepared by the conventional solid-state reaction method. The effects of Ca substitution on the microstructure and dielectric properties was investigated. The X-ray diffraction patterns demonstrated that all the specimens showed perovskite phase, and secondary phases are indicated in the measurement range of X-ray diffraction. Also, all the specimens indicated an rhombohedron phase structure. It was identified from the X-ray diffraction patterns that the secondary phase formed in grain boundaries and then decreased the dielectric properties. For all the specimens, observed one peak was tetragonal cubic phase transition temperature($T_c$), which is located in the vicinity of room temperature.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2004년도 Asia Display / IMID 04
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• pp.1076-1078
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• 2004

In this paper, we report $Eu^{2+}$ activated green phosphor $Ba_2CaMgSi_2O_8:Eu^{2+}$. This phosphor absorbs ultroviolet radation and emits a green visible light. The phosphors were synthesized by conventional solid state reaction method. Reagent grade $BaCO_3$, $CaCO_3$, MgO, $SiO_2$, $Eu_2O_3$ were used as raw materials. The raw materials were mixed thoroughly with an appropriate amount of ethanol in an agate mortar and then dried at 90 $^{\circ}C$ for 2 hours. The mixture was sintered at 900 $^{\circ}C$ for 2 hours and reheated at the mild reducing atmosphere 5% $H_2$ gas mixed with 95% $N_2$ gas at about 900 $^{\circ}C$ to 1250 $^{\circ}C$ for 2 hours. The photoluminescence spectra of the phosphor powders were measured by a fluorescent spectrophotometer. The crystal structure of phosphor powders were investigated by X-ray diffractometer.

• 한국반도체및디스플레이장비학회:학술대회논문집
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• 한국반도체및디스플레이장비학회 2004년도 춘계학술대회 발표 논문집
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• pp.97-100
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• 2004

We report $EU^{2+}$ activated green phosphor $Ba_{2}CaMgSi_{2}O_{8}:Eu^{2+}$. The phosphor absorbs ultroviolet radation and emits a green visible light. The phosphors were synthesized by conventional solid state reaction method. The high purity $BaCO_3$, $CaCO_3$, MgO, $SiO_2$, $Eu_{2}O_{3}$ were used as raw materials. The raw materials were mixed thoroughly with an appropriate amount of ethanol in an agate mortar and then dried at $90^{\circ}C$ for 2 hours. The mixture was sintered at $900^{\circ}C$ for 2 hours and reheated at the mild reducing atmosphere 5% $H_2$ gas mixed with 95% $N_2$ gas at about $900^{\circ}C$ to $1200^{\circ}C$ for 2 hours. The photoluminescence spectra of the phosphor powders were measured by a fluorescent spectrophotometer. The crystal structure of phosphor powders were investigated by X -ray diffractometer.

• Korean Chemical Engineering Research
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• 제55권3호
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• pp.279-286
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• 2017

This review paper evaluates different kinds of synthesis methods for calcite precipitated calcium carbonates by using different materials. The various processing routes of calcite with different compositions are reported and the possible optimum conditions required to synthesize a desired particle sizes of calcite are predicted. This paper mainly focuses on that the calcite morphology and size of the particles by carbonation process using loop reactors. In this regard, we have investigated various parameters such as $CO_2$ flow rate, Ca $(OH)_2$ concentration, temperature, pH effect, reaction time and loop reactor mechanism with orifice diameter. The research results illustrate the formation of well-defined and pure calcite crystals with controlled crystal growth and particle size, without additives or organic solvents. The crystal growth and particle size can be controlled, and smaller sizes are obtained by decreasing the Ca $(OH)_2$ concentration and increasing the $CO_2$ flow rate at lower temperatures with suitable pH. The crystal structure of obtained calcite was characterized by using X-ray diffraction method and the morphology by scanning electron microscope (SEM). The result of x-ray diffraction recognized that the calcite phase of calcium carbonate was the dominating crystalline structure.

• 한국표면공학회지
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• 제51권5호
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• pp.325-331
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• 2018

Calcium carbonate($CaCO_3$) films were formed by an eco-friendly electro-chemical technique on steel substrates in synthesized distilled water solutions containing $NaHCO_3$, $CaCl_2$ and $MgCl_2$ with different ratio respectively. It was investigated to confirm the effect of $Mg^{2+}$ concentration by Scanning Electron Microscopy(SEM), Energy Dispersive x-ray Spectroscopy(EDS) and X-Ray Diffraction(XRD) respectively. From an experimental result, only calcite crystals were found in solution containing no $Mg^{2+}$. By increasing concentration of $Mg^{2+}$, deposition rate decreased and crystal structure was transformed form calcite to aragonite. In case of including $MgCl_2$ 300mM in synthesized solutions containing $NaHCO_3$, $CaCl_2$ 60mM, it was showed over the 90% of aragonite contents which have quite high deposition rate of aragonite. Also, it was confirmed that $Mg^{2+}$ acted as inhibitor on the films which made transforming from calcite to aragonite.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2009년도 하계학술대회 논문집
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• pp.180-181
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• 2009

$(Ba_{0.6},Sr_{0.3}Ca_{0.1})TiO_3$ powders, which were prepared by sol-gel method using a solution of Ba-acetate, Sr-acetate and Ca-acetate and Ti iso-propoxide, $(Ba_{0.6},Sr_{0.3}Ca_{0.1})TiO_3$ array thick films doped with 0.1 mol% $MnCO_3$ and $Yb_2O_3$ (0.1~0.7 mol%) were fabricated by the screen printing method on the alumina substrate. And the structural and electrical properties as a function of $Yb_2O_3$ amount were investigated. The thickness of all (Ba,Sr,Ca)$TiO_3$ thick films was approximately 60mm. The Curie temperature of doped with 0.1 mol% $Yb_2O_3$ specimen was $45^{\circ}C$, and the dielectric constant and at this temperature was 1062.

• 대한화학회지
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• 제46권1호
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• pp.7-13
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• 2002

자화수가 특이한 물리화학적 성질을 갖고 있음은 여러 학자들에 의하여 꾸준히 연구되어 왔는데, 아직도 자화수의 특성이 명확하게 설명되지 못하고 있는 실정이다. 본 연구에서는 자화수가 염류들의 침전반응 및 석고의 가수 경화반응에 미치는 영향을 다음과 같이 관찰하였다. $25^{\circ}C$ 항온조 내부에서 실시한 salt filter assay 방법으로 침전반응을 조사하였으며, $20^{\circ}C$ 실온에서 석고의 가수 경화반응 시간을 Gillmore needle의 방법으로 측정함으로써 석고의 가수 경화 속도를 조사하였다. 0.1M 염 이온들을 반응시킨 염류의 침전 반응 결과, $BaSO_4,\;BaCO_3,\;CaCO_3$의 침전 생성물의 양은 대조군의 증류수에 비하여 자화수에서 각각 약 3.6%, 3.8%, 4.4% 씩 증가되었으며, 석고의 최종 경화시간은 대조군의 증류수에 비하여 자화수에서 현저하게 감소되었으므로 자화수가 석고의 가수 경화속도를 촉진시키는 것으로 나타났다. 이는 대조군의 증류수에 비하여 자화수는 물분자가 치밀하게 구조화되어서 수많은 cluster들을 형성함으로서 물분자 사이의 결합 및 반응력이 증가되며, $Ba^{2+}$ 또는 $Ca^{2+}$ 같은 염류들에 대하여 특징적으로 반응해 침전반응 속도와 가수 경화 반응 속도가 증가된 것으로 추측된다.

• 한국결정학회지
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• 제15권2호
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• pp.59-68
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• 2004

부분적으로 $Co^{2+}$ 이온으로 치환된 제올라이트 A를 진공 탈수한 후 $300^{\circ}C$에서 12시간, 6시간, 2시간 동안 각각 0.6 torr의 K증기로 반응시킨 3개의 구조$(a=12.181(1)\;{\AA},\; a=12.184(1)\;{\AA},\; a=12.215(1)\;{\AA})$를 $21^{\circ}C$에서 입방공간군 Pm3m를 사용하여 단결정 X-선 회절법으로 해석하고 정밀화한다. K 증기로 반응시킨 3개의 구조는 Full-matrix 최소자승법 정밀화 계산에서 $1>\sigma(I)$인 70, 82, 80개의 독립반사를 각각 사용하여 최종오차인자를 R (weight) = 0.090, 0.091, 0.090까지 각각 정밀화한다. 3개의 구조에서 4개의$Co^{2+}$이온과 4개의 $Na^+$이온모두 K증기에 의해서 환원되어 $Co^{2+}$ 이온과 $Na^+$ 이온은 제올라이트 내에 더 이상 생성되지 않는다. K종류는 5개의 다른 결정학적 자리에 위치하는데 3개의 $K^+$이온은 8-링의 평면에 완전히 채워져 위치하고 약 11.5개의 $K^+$ 이온은 3회 회전축상의 6-링에 위치하고 약 4개는 큰 동공, 4개는 소다라이트 동공, 0.5개는 큰 공동의 4-링과 마주보는 위치에 위치하고 3개의 $K^0$원자는 3회 회전축상의 큰 동공 깊숙이 위치한다. 이들 구조는 제올라이트 A의 소다라이트 동공에서 사면체 $K_4$ (혹은 삼각형 $K_3$) 클라스터를 이루고 있으며 $K_4$ 혹은 $K_3$ 클라스터는 6-링의 3개의 산소와 삼면체로 결합한다. 이들 클라스터의 부분적으로 환원된 이온은 제올라이트 골조 산소와 우선적으로 결합한다. 이들 구조에서 제올라이트 골조의 음전하를 상쇄시키는데 필요한 12개의 $K^+$ 이온보다 많은 단위세포당 14.5개의 K종류가 존재하는데 이들 결과로 $K^0$원자가 흡착되었음을 알 수 있다. 큰 동공 깊숙이 위치한 3개의 $K^0$ 원자는 4개의 큰 동공에 위치한 $K^+$ 이온 중 3개와 결합하여 $K_7^{4+}$클라스터를 형성하며$K_7^{4+}$ 클라스터는 골조산소와 우선적으로 결합한다.