• Journal of the Korean Society of Propulsion Engineers
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• v.2 no.3
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• pp.47-53
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• 1998

Using Michael Reaction, commercially available 3-aminopropyltrimethoxysilane and N-[3-(trimethoxysilyl)propuyl]ethylenediamine were reacted with various Michael acceptors, ethyl acrylate, acrylonitrile, acrylamide, 2-cyanoethyl acrylate, 2-hydroxyethyl acrylate and 3-(trimethoxysilyl)propylmethacrylate, to the new aminosilanes. All compounds which are [3-(N-2-carboethoxyethyl)aminopropyl]triethoxysilane, [3-(N-2-cyanoethyl)aminopropyl]triethoxysilane, [3-(N-di-2-car-boethoxyethyl)aminopropyl]triethoxysilane, [3-N-di-cyanoethyl) aminopropyl]triethoxysilane, [3-(N-2-cyanoethoxypropionyl)aminopropyl]triethoxysilane, [3-(N-di-2-cyanoethoxypropionyl)aminopropyl]triethoxysilane, [3-(N-di-2-hydroxyethoxy propionyl)aminopropyl]triethoxysilane, [3-(N-2-amidoethyl)aminopropyl]triethoxysil-ane,｛3-[N-(N-di-2-cyanoethyl)ethyl]aminopropyl｝triethoxysilane and ｛3-[N-(3-trimethoxysilylpropyl)-2-methylpropionyl]aminopropyl｝triethoxysilane were succes-sfully prepared in 35-70% yields and which were identified with $^1{H}$-NMR and FT-IR spectroscopy.

• Polymer(Korea)
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• v.39 no.1
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• pp.169-173
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• 2015

Metallocene was supported on the silica, which was functionalized with aminosilanes such as aminopropyltrimethoxysilane (1NS) or N-[3-(trimethoxysilyl)propyl]ethylenediamine (2NS), and ionic liquids such as 1-butyl-4-methylpyridinium chloride (Cl), tributylmethylammonium chloride (Amm), benzyldimethyltetradecylammonium chloride (Ben), 1-butyl-1-methylpyrrolidinium chloride (Pyr), and then ethylene polymerizations were performed. The Zr contents of $SiO_2/1NS/IL/(n-BuCp)_2ZrCl_2$ and $SiO_2/2NS/IL/(n-BuCp)_2ZrCl_2$ were lower than those of only aminosilane-treated silicas. However, the polymerization activity of $SiO_2/1NS/IL/(n-BuCp)_2ZrCl_2$ was higher than that of $SiO_2/1NS/(n-BuCp)_2ZrCl_2$. The polymerization activity of $SiO_2/2NS/IL/(n-BuCp)_2ZrCl_2$ was lower than that of $SiO_2/2NS/(n-BuCp)_2ZrCl_2$ due to much lower Zr content.

• Journal of the Microelectronics and Packaging Society
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• v.29 no.4
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• pp.15-20
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• 2022

Aerogel is a material having a nanopore structure based on a high porosity. Due to this high porosity, it has excellent properties not found in conventional materials, but its application has been limited due to low mechanical strength. Therefore, to improve the mechanical strength of the aerogel, polyurea crosslinking was introduced and a precursor having an amine group essential for polyurea polymer formation was selected to synthesize a polyurea crosslinked aerogel composite. In addition, the crosslinking of polyurea was adjusted according to the number of amine groups present in aminosilane. It was confirmed through various analyses that the nanopore structure of the aerogel was maintained to have mesopores. The aerogel thus formed was able to improve the mechanical strength by about two times, and it was confirmed through field emission scanning electron microscope analysis that a one-dimensional polymer was formed on the silica aerogel surface through the introduction of ethylene diamine. The one-dimensional polymer thus formed has improved mechanical properties, resulting in securing an elastic modulus of about 2.66 MPa.

• Proceedings of the Polymer Society of Korea Conference
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• 2006.10a
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• pp.204-204
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• 2006

The interfacial interaction along with microstructure and some properties of the polyimide(PI)/silica or polyimide/silsesquioxane hybrid nanocomposites will be discussed with reviewing recent publications including our own works. Poly(vinyl silsesquioxane) (PVSSQ), aminosilane (APS), and titania can effectively play vital roles to compatibilize the PI/silica hybrid composites by enhancing interfacial interaction or reducing agglomeration of large domains, which helps the formation of nanocomposites for the PI/silica hybrid system.

• Polymer(Korea)
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• v.30 no.4
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• pp.318-325
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• 2006

Polypropylene-clay nanocomposites were studied by the modification of clay with amino silanes to introduce covalent bonds in nanocomposites, and prepared by melt-compounding with polypropylene, clay modified with amino silanes and maleic anhydride grafted polypropylene. The . .structure and surface properties of modified clay were determined by x-ray diffraction, infrared spectrum, and solid-state $^{29}Si$ nuclear magnetic resonance spectrum. The modification of clay with aminosilanes led to the increase of the silicate interlayers to about $19.8{\AA}$, the weakening effects of hydroxy group at $3650cm^{-1}$ and the signal of amine groups at -69 ppm proved that the modification had taken place.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2001.07a
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• pp.78-83
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• 2001

In this work, the surface of inorganic fillers were modified with some functional groups such as stearic acid, aliphatic long chain, vinylsilane and aminosilane to control the interaction between inorganic fillers and polymer matrix. Ethylene-vinyl acetate copolymers (EVA) with various amount of vinyl-acetate content and copolyether-ester elastomer were used as polymer matrix. The addition of inorganic fillers increases flame retardancy, but results in steep drop of electrical and mechanical properties, which may be caused by the defect in the interface between organic/inorganic hybrid composites. The hybrid composites are found to show better mechanical properties and higher volume resistivities as inorganic fillers are well dispersed and have good adhesion with polymer matrix. Also, the most effective type of functional group coated on fillers depends on the chemical structure of polymer.

• Proceedings of the Korean Vacuum Society Conference
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• 2011.02a
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• pp.111-111
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• 2011

유기박막트랜지스터는 각 박막계면의 접촉성에 따라 그 성능이 좌우 된다는 것은 널리 알려진 사실이다. 이 때문에 계면간의 접촉성 및 결함을 최소화 하고 효율적인 패턴 형성을 위해 자기조립단분자막의 이용이 최근에 많이 시도되고 있다. 고품질 자기조립단분자막의 제작을 위해 RCA 세척을 통해 웨이퍼 표면에 OH기를 도입 보다 완벽한 단분자막의 형성을 촉진 하였으며 패턴제작은수분이엄격이조절된환경에서 alkyilsilane과 aminosilane 자기조립단분자막을 각각 ${\mu}CP$과 용액공정을 통해 시도되었다. 이 과정에서 물리적 흡착이나 OH기 부족으로 생성된 결함을 보안하기 위하여 SC1용액을 사용 단순 물리흡착된 자기조립단분자 물질의 제거와 다시 OH기 도입 용액공정을 통해 자기조립단분자막 형성을 반복적으로 실시하였다. 그 결과 자기조립단분자막의 결함이 최소화 되었고 자기조립단분자막의 질에 따라 유기전극재료 증착 시 선택적인 성장 과 형성된 유기전극재료 층의 형상이 다르게 관찰 되었다. 이런 반복적인 용액공정을 통해 결함이 최소화된 고품질 자기조립단분자막은 박막계면 간 옴성접촉을 형성하여 유기박막트랜지스터 제작 시 성능 향상이 기대되어진다.

• Proceedings of the KIEE Conference
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• 1987.11a
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• pp.216-219
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• 1987

Dielectric and Mechanical Properties of Mica flake/ Epoxy Composite are investigated. The Mica content is about 50 wt % and its thickness is about $240{\mu}m$. The finished Mica flake/Epoxy Composite contains about 0.1-1.0 wt % of aminosilane coupling agent. Ruby Mica filler and high temperature curing Epoxy resin are used. From the viewpoint of dielectric and mechanical properities. the optimum properties is obtained for the sample post cured at $130^{\circ}C$ for 5 h ours after curing at $80^{\circ}C$ for 2 hours and with 0.5 weight % silane coupling agent.

• Fisheries and Aquatic Sciences
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• v.8 no.3
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• pp.122-127
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• 2005

A DNA chip that rapidly and accurately detects the viral genes in rhabdovirus-infected fish was developed. The N, Ml, and G proteins of three rhabdovirus strains, infectious hematopoietic necrosis virus (IHNV), viral hemorrhagic septicemia virus (VHSV), and flounder rhabdovirus (HIRRV), were selected for use as probes. The sequences of the corresponding genes were obtained, and probes were prepared by PCR using specific primer sets. The specificity of the probes was confirmed by cross PCR. The prepared probes were spotted on poly-L-lysine- or aminosilane-coated glass slides and hybridized with target DNA under several different conditions in order to determine the optimal hybridization temperature, glass-slide coating, and target cDNA concentration.

• Journal of the Korean Chemical Society
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• v.25 no.2
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• pp.119-123
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• 1981

Trimethyldiethylaminosilane, trimethylanilinosilane, trimethyldiethylaminostannane and trimethylanilinostannane were reacted with phenylisocyanate at various temepturares. All the reactions below $100^{circ}C$ gave only triphenylisocyanurate, but above $150^{circ}C$, diphenylcarbodiimide also was produced considerably. The reaction rate of anilinosilane was faster than that of aminosilane, but in the case of stannanes, the amino compound was more reactive.