• 한국의류산업학회지
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• 제6권5호
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• pp.667-672
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• 2004

Poly(ethylene terephthalate) (PET) fabrics were treated with a silica particle and phosphate flame retardant to determine the optimum process condition of the digital textile printing(DTP) media. The treating conditions for the study were 6 conditions, from F1 to F6, in which F3, F4 and F5 were treated with mixture of both silica particle and phosphate compound in process of pad, dry and cure fixation. F6 was treated with phosphate compound only and silica particle coating successively. Xanthan gum was used to control the migration of liquid phosphate compound onto PET fabrics. The change in surface morphology of fabrics treated with silica particle and phosphate compound was observed by SEM and flame retardance was evaluated by limiting oxygen index(LOI). It was observed that F6 was the excellent flame retardance and low bleeding in printing, Collectively, the printing characteristics of silica to cyan, magenta, yellow and black ink and flame retardance of fabrics finished with phosphate compound were identified in this study.

• 한국재료학회지
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• 제15권11호
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• pp.717-721
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• 2005

Silica powders were synthesized using emulsion solution containing water, nonionic surfactant of Triton N-57, and cyclohexane. Silica powders were prepared at low cost using inexpensive starting material of sodium silicate and ammonium sulfate. Morphology, size and size distribution were observed and determined using SEM. The powder was identified as silica by FT-IR and XRD analysis. Particle size and size distributions were affected by concentration of reactants, reaction time, and concentration of surfactant. Particle size were increased with increasing concentration of reactants and particles became dense with increasing reaction time. As R value increased, tile particle size was increased, reached a certain value and then decreased again. The silica powders synthesized under optimum condition were spherical in shape, $0.8{\mu}m$ in average particle size, narrow in particles size distribution, and well dispersed.

• 한국전기전자재료학회논문지
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• 제32권3호
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• pp.246-251
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• 2019

A solvent free, highly concentrated silica-acryl monomer hybrid sol was synthesized using aqueous colloidal silica as a precursor. The effects of the silica particle size, type of surface treatment agent employed, and silica content on the formation of the hybrid sol were systematically studied. The optical and physical properties of the coating solution prepared using the hybrid sol were also characterized. The viscosity of the hybrid sol tended to decrease as the particle size of the silica and the molecular weight of the surface treatment agent increased. The PET substrate coated with MPTMS-Mix (mixture, 70 wt%) solution showed the highest surface hardness (6 H) and low surface roughness ($Ra=0.044{\mu}m$), which could be attributed to an increase in packing density caused by the infiltration of small particles into the pores formed between larger particles.

• Elastomers and Composites
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• 제56권1호
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• pp.32-42
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• 2021

The vulcanizate structure of silica-filled compounds is affected by the filler-rubber interaction (FRI) due to the silica-rubber coupling reaction and the chemical crosslink density (CCD) of the matrix rubber. In this study, the vulcanizate structure changes of silica-filled compounds according to the silane and sulfur variation were quantitatively analyzed using the Flory-Rehner and Kraus equations. In efficiency vulcanization (EV) conditions with low sulfur content, FRI increased when the bis-[3-(triethoxysilyl)propyl]tetrasulfide (TESPT) content increased, and the CCD clearly decreased. By contrast, in semi-EV conditions with high sulfur content, as TESPT content increased, the FRI increased the same way EV conditions, but the CCD was unchanged. Based on these results, it was confirmed that FRI of the silica-filled compounds increased as TESPT content increased, but CCD decreased or retained similar values according to the vulcanization system, indicating that the formation reaction of FRI was preferred over CCD.

• 한국태양에너지학회 논문집
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• 제33권6호
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• pp.39-46
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• 2013

This work introduces a simple one-reactor adsorption desalination system that harnesses low temperature heat sources (solar energy, waste heat), which has been experimentally studied to elicit the most suitable design parameters and operating conditions. The design process of the system was divided into three parts to reflect the operating principle of desalination technology with application of adsorption processes. First, the evaporator for the vaporization of saline water was designed, then the reactor for the adsorption and release of the steam, followed by the condenser for condensation of the fresh water. The specific water yield is measured experimentally with respect to the time while controlling parameters such as heat source temperatures, coolant temperatures, system switching and half-cycle operational times. The present system well demonstrates the applicability of silica gel in relation to adsorption technologies that utilize low temperature heat sources ranging from 60 to $80^{\circ}C$, such as solar energy and waste heat.

• 멤브레인
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• 제24권3호
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• pp.177-184
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• 2014

본 연구에서 고투과도를 갖는 실리카 분리막은 콜로이달 실리카 졸과 고분자형 실리카 졸 두 가지를 DRFF법과 SRFF법으로 다공성 금속 지지체 위에 코팅하여 제조되었다. 실리카 졸은 졸-겔법으로 테트라에톡시실란(TEOS)에 의하여 제조되었고, 각각의 졸은 동적광산란법(DLS), 전계방사 주사전자현미경(FE-SEM), 질소 흡착법 등을 이용하여 그 특성을 평가하였다. 다공성 금속 지지체위에 콜로이달 실리카 졸로 중간층을 형성하여 치밀한 구조의 실리카 층을 형성한 후 그 위에 분리층으로 고분자형 실리카 졸을 코팅하여 핀홀을 줄이는 방법으로 기체분리용 분리막을 제조하였다. FE-SEM으로 분리막의 코팅 층을 분석한 결과 분리층은 중간층보다 침밀한 구조를 가지고 있음을 확인하였고 기체투과 결과 수소 투과도 $(6.63-9.21){\times}10^{-5}mol{\cdot}m^{-2}{\cdot}s^{-1}{\cdot}Pa^{-1}$ 분포를 보였다.

• Bulletin of the Korean Chemical Society
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• 제30권9호
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• pp.1978-1980
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• 2009

A mesostructured form of carbon was fabricated from a template of mesostructured silica by using pentane, an aliphatic hydrocarbon precursor. To synthesize the mesostructured silica, a buffered (pH of 6.5) mixture of nonionic Pluronic P123 surfactant, sodium silicate, and acetic acid were used. The impregnated silica with Fe$(CO)_5$ (wt 5%) and pentane was placed in a quartz tube, treated with pentane vapor at 800 ${^{\circ}C}$ for two hours to synthesize the mesostructured carbon. The XRD patterns of the carbon replica in the low/wide angle regions, its TEM images, and nitrogen adsorption-desorption isotherm revealed that the long-range framework order of mesostructure with the pore size centered on 2.8 nm was maintained to some extent mainly due to some portions of mesophase carbon that work as a support to fix the hexagonal frameworks by anchoring on the pore surface with an improved graphitic character. The dc conductivity of the mesostructured carbon in pressed powder form at 6.0 MPa was 2.08 S/cm.

• 센서학회지
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• 제16권1호
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• pp.77-83
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• 2007

Nanoporous silica aerogels with various surface modifiers were prepared by ambient drying process. Tetraethylorthosilicate (TEOS) were used a raw material. Ambient drying process for various surface modifier was studied in the point of view of a crack-free monolith and thin films and low cost. Various kinds of surface modifiers like as hexamethyldisilazane (HMDSZ), trimethlychlorosilane (TMCS), methlytriethoxylsilane (MTES), and methlytrimethoxysilane (MTMS) were studied in order to enhance hydrophobicity for the silica aerogel. Surface modified aerogels were evaluated by FT-IR, TG, BET, SEM and wetting angle measurement. Homogeneous and crack-free aerogels were obtained by modifying the HMDSZ and the TMCS. However silica xerogel was obtained when modified with MTMS, MTES.

• Macromolecular Research
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• 제15권2호
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• pp.134-141
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• 2007

The direct chromatographic separation of enantiomers by chiral stationary phases (CSPs) has been extensively developed over the past two decades, and has now become the most popular method for the analytical and preparative separations of enantiomers. Polysaccharide derivatives coated onto silica gel, as CSPs, playa significantly important role in the enantioseparations of a wide range of chiral compounds using high-performance liquid chromatography (HPLC). Unfortunately, the strict solvent limitation of the mobile phases is the main defect in the method developments of these types of coated CSPs. Therefore, the immobilization of polysaccharide derivatives onto silica gel, via chemical bonding, to obtain a new generation of CSPs compatible with the universal solvents used in HPLC is increasingly important. In this article, our recent studies on the immobilization of polysaccharide derivatives onto the silica gel, as CSPs, through radical copolymerization with various vinyl monomers are reported. Polysaccharide derivatives, with low vinyl content, can be efficiently fixed onto silica gel with high chiral recognition.

• 마이크로전자및패키징학회지
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• 제26권2호
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• pp.23-29
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• 2019

Thermally expandable microsphere and aerogel composite was prepared by chemical compositization. Microsphere can produce synergies with aerogel, especially an enhancement of mechanical property. Through condensation between sulfonated microsphere and hydrolyzed silica sol, chemically-connected composite aerogel could be prepared. The presence of hydroxyl group on the sulfonated microsphere was observed, which was the prime functional group of reaction with hydrolyzed silica sol. Silica aerogel-coated microsphere was confirmed through microstructure analysis. The presence of silicon-carbon absorption band and peaks from composite aerogel was observed, which proved the chemical bonding between them. A relatively low thermal conductivity value of $0.063W/m{\cdot}K$ was obtained.