• 한국산학기술학회논문지
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• 제12권11호
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• pp.5365-5369
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• 2011

실리카-골드 복합체 입자를 함침법에 의하여 합성하였고, 용매와 전구체가 실리카-골드 입자 합성에 미치는 영향이 연구되었다. 구형 실리카 입자를 지지체로 하여 PVP, hydrogentetrachloroaurate(III) hydrate 수용액을 전구체로 사용했을 때, 연한 분홍색 색상을 띄는 실리카-골드 입자가 성공적으로 합성되었다. 합성된 복합체의 특성은 FE-SEM, FE-TEM과 XRD를 통하여 분석하였다.

• Nuclear Engineering and Technology
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• 제55권7호
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• pp.2547-2555
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• 2023

Amberlite IRN-78 resin was incorporated with iron to make a hybrid resin for the removal of silica from the borated water of nuclear power plants. The hybrid resin contained 0.84 wt % iron compounds upon pyrolysis. In batch experiments carried out at room temperature, 1 g of the hybrid resin removed ~60 ㎍ silica from 1 ppm borated water in ~120 min. The efficiency of the hybrid material increased with the resin quantity, decreased with silica concentration, and remained unchanged at different pH values. Freundlich and Temkin isothermal adsorption dominated the silica removal process and followed the pseudo-first-order and intra-particle diffusion mechanism simultaneously. The concentration of the leached iron remained appreciably under the safe limits of 200 ㎍/l during the experiments. This detailed study suggests the use of hybrid resin for the removal of silica from borated water streams and other similar systems.

• 한국산학기술학회논문지
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• 제20권5호
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• pp.1-6
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• 2019

유기 염료가 도핑 된 실리카 나노입자는 바이오 라벨링, 바이오 이미징 및 바이오 센싱에 사용되고 있는 유망한 나노소재이다. 일반적으로 형광 실리카 나노입자는 수정된 스토버 방법($St{\ddot{o}}ber$ Method)으로 합성된다. 본 연구에서는 다양한 크기를 갖는 염료가 첨가되지 않은 형광 실리카 나노입자를 수정된 스토버 합성법인 졸겔 공정으로 합성하였다. 졸겔 공정 중에 기능성 물질인 APTES를 첨가제로 첨가하였다. 졸겔 공정으로 합성된 실리카 나노입자는 $400^{\circ}C$에서 2시간 동안 하소되었다. 합성된 실리카 나노입자의 표면형상과 크기를 전계방출 주사전자현미경으로 조사하였고, 합성된 실리카 나노입자의 형광 특성은 파장 365 nm의 자외선 램프를 조사하여 확인하였다. 또한 합성된 실리카 나노입자의 광발광 (PL) 특성을 형광 분석 형광법으로 조사하였다. 그 결과 합성된 실리카 나노입자는 입자의 크기와 무관하게 모두 청색 형광 특성을 갖는 것으로 확인되었다. 특히, 실리카 나노입자의 크기가 증가할수록 PL 강도는 감소하였다. 염료가 첨가되지 않은 실리카 나노입자의 청색 형광 특성은 APTES 층의 $NH_2$ 기능기와 실리카 매트릭스 뼈대 내부의 산소관련 결함과의 결합에 기인하는 것으로 추정된다.

• International Journal of Concrete Structures and Materials
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• 제18권1E호
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• pp.63-70
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• 2006

This study tested the alkali-silica reactivity of various types of crushed stones, following the specifications of ASTM C 227 and C 1260, and the results obtained from the tests were compared. This study also analyzed the effects of particle size and grading of reactive aggregate based on the expansion of mortar-bar due to an alkali-silica. The effect of mineral admixtures to reduce the detrimental expansion caused by the alkali-silica reaction was investigated based on the method specified by ASTM C 1260. The mineral admixtures used in this study were fly ash, silica fume, metakaolin and ground granulated blast furnace slag. The replacement ratios of 0, 5, 10, 15, 25 and 35% were uniformly applied to all the mineral admixtures, and the replacement ratios of 45 and 55% were additionally applied for the admixtures that could sustain the workability at these ratios. The results indicate that replacement ratios of 25% for fly ash, 10% for silica fume, 25% for metakaolin and 35% for ground granulated blast furnace slag were the most effective in reducing the expansion due to the alkali-silica reaction under the experimental conditions of this study.

• 한국환경과학회지
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• 제21권7호
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• pp.787-795
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• 2012

The purpose of this study is to synthesize transition metal doped mesoporous silica catalyst and to characterize its surface in an attempt to decomposition of $N_2O$. Transition metal used to surface modification were Ru, Pd, Cu and Fe concentration was adjusted to 0.05 M. The prepared mesoporous silica catalysts were characterized by X-ray diffraction, BET surface area, BJH pore size, Scanning Electron Microscopy and X-ray fluorescence. The results of XRD for mesoporous silica catalysts showed typical the hexagonal pore system. BET results showed the mesoporous silica catalysts to have a surface area of 537~973 $m^2/g$ and pore size of 2~4 nm. The well-dispersed particle of mesoporous silica catalysts were observed by SEM, the presence and quantity of transition metal loading to mesoporous surface were detected by XRF. The $N_2O$ decomposition efficiency on mesoporous silica catalysts were as follow: Ru>Pd>Cu>Fe. The results suggest that transition metal doped mesoporous silica is effective catalyst for decomposition of $N_2O$.

• 한국재료학회지
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• 제26권6호
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• pp.306-310
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• 2016

To produce 4N grade high-purity silica powder from natural ore, the mineralogical characteristics of natural silica ore were investigated and their effects on the purification process were revealed. The Chinese silica mineral ore used was composed of iron and aluminum as main impurities and calcium, magnesium, potassium, sodium, and titanium as trace impurities; these trace impurities generally exist as either single oxides or complex oxides. It was confirmed that liberation and acidic washing of the impurities were highly dependent on the particle size of the ground silica ore and on its mineralogical characteristics such as the distribution and phases of existing impurities. It is suggested that appropriate size reduction of silica ore should be realized for optimized purification according to the origin of the natural silica ore. A single step purification process, the mechano-chemical washing (MCW) process, was proposed and verified in comparison with the conventional multi step washing process.

• 한국자기공명학회논문지
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• 제4권1호
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• pp.50-63
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• 2000

Titanium dioxide particles with three different average sizes, prepared by three different methods, were incorporated into silica gel pores by impregnation. The titanium dioxide incorporated into the silica gel pores was photoionized by 240-400 nm irradiation at 77 K by a one-photon process to from trapped hole centers on OH group and trapped electron centers on titanium which were detected by electron paramagnetic resonance at 77 K. During the impregnation the smallest size range of TiO2 particles can be incorporated into silica gels with 2.5-1.5 nm pores. However, the largest size range of TiO2 particles can only be incorporated into silica gels with 6-15 nm pores and not into silica gels with 2.5-4 nm pores. The photoyield and stability of photoinduced hole and electron centers depends on the silica pore sizes of silica gels and surface area as well as on the TiO2 loading. In large pore silica gels and large particle size of TiO2, photoinduced charge separation reaches to a plateau at shorter irradiation times and the trapped hole and electron centers are more stable to decay.

• 공업화학
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• 제17권4호
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• pp.386-390
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• 2006

콜로이드형 실리카는 화학적으로 안정한 무기소재로 비표면적과 표면물성이 우수하여 산업적으로 다양한 용도로 사용하고 있다. 본 연구에서는 sodium silicate로부터 이온교환방법 및 산-중화법을 이용하여 colloidal silica를 제조하고 입자성장인자인 온도, pH, 농도와 aging time을 조절하여 크기를 조정하는 방법을 조사하여 균일한 크기분포를 가진 colloidal silica를 제조하였다. 실리카 졸의 크기와 모양은 TEM 및 dynamic scattering method를 이용하여 측정하였다. 또한 콜로이드의 입자크기에 따른 제타 전위값의 변화, 겔화현상과 그 유변학적 특성을 연구하였다.

• 한국세라믹학회지
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• 제40권7호
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• pp.696-701
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• 2003

교반형 볼 밀에서 실리카 분말의 열처리에 따른 분쇄효율을 분쇄에 따른 에너지 소비량을 측정함으로써 조사하였다. 열처리를 행한 것과 행하지 않은 시료를 비교해 보면, 600~90$0^{\circ}C$에서 열처리 후 실온에서 냉각된 시료를 건식 분쇄하였을 경우 약 40~50% 정도, 열처리 후 물속에서 급속 냉각한 경우 약 52～62% 정도의 에너지의 감소 효과가 있었다. 또한 열처리한 실리카 분말을 습식 분쇄를 할 경우 건식 분쇄에 비하여 약 40% 정도의 분쇄에너지가 적게 소모되고 있음을 알 수 있었다. 또한 실리카 분말을 열처리 한 후, 급속 냉각할 경우 발생하는 열충격은 입도에 대한 영향을 거의 받지 않으며 분쇄효과를 향상시킴을 알 수 있었다.

• 한국전기전자재료학회논문지
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• 제31권7호
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• pp.496-501
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• 2018

In this study, we prepared 40, 45, 50, 55, 60, 65, and 70 wt% content composites filled in epoxy matrix for two micro silica and three micro alumina types for use as a GIS heavy electric machine. As a filler type of epoxy composite, micro silica composites showed excellent AC breakdown strength properties compared to micro alumina composites in the case of electrical properties of micro silica and alumina. The electrical breakdown properties of micro silica composites increased with increasing filler content, whereas those of micro alumina decreased with increasing filler content. In the case of mechanical properties, the micro silica composite showed improved tensile strength and flexural strength compared with the micro alumina composite. In addition, mechanical properties such as tensile strength and flexural strength of micro silica and alumina composites decreased with increasing filler content. This is probably because O-H groups are present on the surface of silica in the case of micro silica but are not present on the surface of alumina in the case of micro alumina.