• 공업화학
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• 제24권2호
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• pp.148-154
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• 2013

UV 경화형 아크릴 점착제는 세상에서 매우 다양한 형태로 이용되는데, 반도체 산업을 기반으로 하는 웨이퍼 제조공정에서도 이용되고 있다. 특히 반도체에 사용되는 웨이퍼가 더욱 얇아짐에 따라, UV 경화형 아크릴 점착제는 더욱 적절한 점착 성능을 요구 받고 있다. 본 연구는 2-EHA (2-ethyl hexyl acrylate), 2-EHMA (2-ethyl hexyl methacrylate), SM (styrene monomer), 2-HEA (2-hydroxy ethyl acrylate), acrylic acid 모노머를 이용하여 hydroxy기를 가진 아크릴 수지점착제를 합성한 후 MOI (methacryloyloxyethyl isocyanate)의 투입량 조절을 통한 경화 특성을 향상시킬 수 있는 부가반응을 시킨 이소시아네이트 변성 아크릴 수지 점착제를 제조하여, 적절한 접착 성능을 알아보고, 수산기 값의 정도와 UV 조사량의 차이에 따라 웨이퍼 제조의 최적화된 조건을 찾았다. 시험 결과 UV 경화형 점착제에서 수산기(Hydroxyl group, -OH)와 이소시아네이트기(isocyanate group, -NCO)의 1 : 1 당량비로 이소시아네이트 경화제를 사용할 경우 수산기값이 클수록, UV 조사 전 박리력이 감소하였다. UV 조사량이 증가할수록 높은 경화 특성 때문에 박리접착 강도는 낮아졌다.

• 폴리머
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• 제38권6호
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• pp.720-725
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• 2014

Hydride terminated polydimethylsiloxane과 allyl amine을 hydrosilylation 반응으로 aminopropylpoly-dimethylsiloxane을 합성하고, 이를 hexamethylenediisocyanate(HDI)의 고리화 반응으로 제조된 cyclic HDI trimer와 반응시켜 urea결합으로 결합된 polydimethylsiloxane 변성 urea을 제조하였다. Polydimethylsiloxane 변성 urea의 말단에 있는 isocyante기와 2-hydroxyethylmethacrylate를 반응시켜 말단에 multi acrylate기가 도입된 polydimethylsiloxane 변성 urea/acrylate(PUA)를 제조하였다. 제조한 화합물의 구조를 FTIR, $^1H$ NMR로 확인하였으며, PUA에 아크릴계 단량체, 광 개시제, 용매 등을 여러 가지 조성비로 혼합하여 코팅 액을 제조하였으며 이를 PET 필름에 도포하고 UV을 조사하여 고경도의 유연성을 갖는 코팅 막을 제조하였다. 제조한 코팅 막의 연필 경도는 3H, 접촉각은 $82^{\circ}$, bendability는 $7{\phi}$까지 scratch가 발생하지 않았다.

• Korean Chemical Engineering Research
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• 제48권5호
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• pp.568-573
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• 2010

본 연구에서는 polyester 섬유표면에 활성기를 부여하기 위한 전처리제로 isocyanate를 이용하여 농도에 따른 접착력을 평가하였다. 이 후 HNBR compound와 polyester fabric의 접착 시 접착력이 우수한 RFL 용액용 latex 선정 및 F/R mole ratio, F/R resin/latex 무게 비에 따른 실험을 진행하였다. 그 결과 전처리제의 농도가 7 wt%인 경우 가장 높은 접착력을 나타내었으며, RFL 용액용 latex로는 HNBR 컴파운드와 상용성이 높은 NBR latex가 우수한 결과를 나타내었고 F/R mole ratio, FR resin/latex 무게비가 각각 1/1, 20%일 때 가장 높은 접착력을 나타내었다. 또한, peel test와 FTIR 분석을 이용해 RF resin의 열처리 온도에 따른 접착강도와 spectra의 peak 변화를 평가해 본 결과 최적의 열처리 온도는 $200^{\circ}C$이었다.

• Journal of the Korean Wood Science and Technology
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• 제28권1호
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• pp.36-41
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• 2000

목재는 2-메타크릴로일옥시에틸 이소시아네이트(MOI)와 $50-60^{\circ}C$에서 촉매존재하에서 매우 쉽게 반응하였다. 적외선 분광분석을 통하여, 목재가 MOI와 우레탄결합($1715cm^{-1}$)를 형성하고 있을 뿐만 아니라, 올레핀구조의 탄소간 이중결합 ($1635cm^{-1}$)이 존재하고 있음이 밝혀졌다. 도입된 메타크릴산기는 다른 비닐모노머와의 그래프트공중합시 반응시점으로 작용할 것이다. 또한 MOI처리목재는, MOI와의 반응에 의해 친수성이던 목재의 표면이 소수화되어 접촉각이 증대되는 결과를 낳았다. X선광전자분광분석(XPS)의 결과, 목재의 표면부위의 대부분은 MOI에 의해 개질되었음을 밝혀졌다.

• 통합자연과학논문집
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• 제6권1호
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• pp.1-7
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• 2013

Polyurethane resin containing isocyanate is marked by excellent tensile and mechanical strengths and this test aims to gauge its applicability as a medical high polymer. Tris [2-(acryloyloxy)ethyl]isocyanurate and hexamethylenediisocyanate were added to a basic mixing ratio of HEMA (2-hydroxyethyl methacrylate), MMA (methyl methacrylate), NVP (n-vinyl-2-pyrrolidone) and crosslink agent, EGDMA (ethylene glycol dimethacrylate) with increasing proportions and copolymerized respectively. Also, the basic physical properties of the polymerized high polymers including refraction rate, tensile strength, light transmission and water content were measured to confirm that they are appropriate as hydrogelcontact lenses. After measuring the physical properties of high performance polymers produced by adding tris [2-(acryloyloxy) ethyl]isocyanurate, it was found that the average tensile strengths of sample TRIS1 to TRIS10 were between 0.285 and 0.612 kgf, while the average values of refractive index were ranged from 1.441 to 1.449 with water content from 30.00 to 37.35%.The measurement of physical properties of the copolymers generated by adding hexamethylenediisocyanate showed that the average tensile strength of sample HEXA1 to HEXA10 ranged from 0.267 to 1.742 kgf, the refractive index ranged from 1.443 to 1.475 and water contents were in the range of 21.22 to 35.58%. In all combinations the transmission rates satisfied the transmittance of general hydrogel contact lenses. From theresults, it is possible to conclude that the produced copolymers can be used as contact lens materials with excellent tensile strength.

• Journal of the Korean Wood Science and Technology
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• 제31권5호
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• pp.23-34
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• 2003

본 연구는 국산소경재인 소나무(Pinus densiflora)재와 낙엽송(Larix kaemferi)재로 제조된 유리섬유강화 집성재의 강도적 성질을 조사해 보기 위하여 실시되었다. 먼저, 직물 유리섬유를 수성고분자-이소시아네이트계(MPU-500) 접착제를 사용하여 control재와 유리섬유를 각각 1층과 2층 함입하였다. 본 연구의 결과는 다음과 같다. 1. 수성고분자-이소시아네이트 수지는 집성재 제조용으로 적합하였으며, 특히 유리섬유를 2층 함입한 소재를 제외하고는 구조용 집성재의 품질기준(KS F 3021)을 만족시켰다. 2. 직물유리섬유를 함입할 경우 휨강도, 전단강도에서 control재보다 크게 뛰어나지는 않았지만, 비례한도 휨응력은 유리섬유의 함입 층수에 비례하여 증가하였다. 그러므로, 직물 유리섬유의 mesh수와 두께를 집성재 소재의 형태에 따라 적절히 조정한다면, 휨강도와 전단강도를 좀더 향상시킬 수 있을 것으로 판단되었다.

• Archives of Pharmacal Research
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• 제28권4호
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• pp.382-390
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• 2005

chial allylic ethers with a hydroxyl group attached to the $\pi-system$ and chlorosulfonyl isocyanate. The enantioselectivity of the CSI reaction with the chiral allylic and benzylic ethers was examined in various solvents and temperatures. Based on these results, it was proposed that the CSI reaction is a competitive reaction of a $S_{N}i$ (retention) and a $S_{N}1$ mechanism (racemization) according to the stability of the carbocation intermediate. This means that there is a greater proportion of retention with the less stable the carbocation intermediate and vise versa.

• 통합자연과학논문집
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• 제11권2호
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• pp.113-120
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• 2018

This study was planned to prepare the high strength hydrogel ophthalmic lens containing isocyanate group and nanoparticles. HDI with carbon nanoparticles were used as additives for the basic combination of HEMA, MA and MMA, and the materials were copolymerized with EGDMA as the cross-linking agent and AIBN as the initiator. The mixture was heated at $100^{\circ}C$ for an hour to produce the high performance hydrogel ophthalmic lens by cast mold method. Measurement of the physical characteristics of the produced material showed that the refractive index was in the range of 1.4027~1.4600, water content 25.21~44.01%, contact angle $54.18{\sim}72.94^{\circ}$, visible light transmittance 53.03~92.09%, and tensile strength 0.1024~0.2359 kgf and breaking strength was 0.0872~0.2825 kgf. The results showed an increase of refractive index while the decrease in water content. And also, the breaking strength was highest when the addition ratio of HDI was 5%(wt). As a result of the absorbance measurement, no significant difference was observed in all the samples, so it can be judged that the stabilization of nanoparticles in the polymer was maintained.

• Advances in materials Research
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• 제13권2호
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• pp.129-140
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• 2024

This study evaluates the ratio of Toluene di-isocyanate (TDI) functional group isocyanate (NCO) to the binder functional hydroxyl group (OH) in HTPB/AP/Al-based propellants on their mechanical properties, flow rate, and viscosity to determine the limitations of NCO/OH in the composition of solid propellants. The propellants consisted of hydroxyl-terminated polybutadiene (HTPB) polyurethane (PU), aluminum (Al) and tri-modal ammonium perchlorate (AP). The tri-modal AP consisted of 30% of coarse AP, 30% of medium AP, and 8% of fine AP. The ratio of NCO/OH varies from 0.73 to 0.85, with two binder percentages of 10.5% and 12%. An increase in NCO/OH ratio with 10.5% binder provided 20%, 95%, and 8 to 9% increments in UTS, modulus, and hardness, respectively. However, the propellant elongation, density, and flow rate decreased by 170%, 0.2%, and 11-12%, respectively. Viscosity increased 20% based on initial hour reading. The 12% binder provides 27%, 47%, and 5~6% an increment of UTS, modulus and hardness respectively. However, the propellant elongation, density, and flow rate decreased by 47%, 0.17% and 27%, respectively. The viscosity increased 30% based on initial hour reading. This study suggests the NCO/OH value of 0.77 and 10.5~11% binder content in propellant based on the mechanical properties, flow rate, and viscosity for better processing and pot life.

• 약학회지
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• 제29권1호
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• pp.39-42
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• 1985

Betaines of bicyclic imidazo-thiazoles were synthesized by the reaction of clectrophiles such as methyl isocyanate, methyl isothiocyanate, allyl isothiocyanate and ketene with 3-methyl and 3-phenyl-5, 6-dihydroimidazo [2,1-b] thiazole. In this reaction, the methyl group which was substituted at 3-position increased the yields of the products in comparison with those from phenyl group substituted substrates. Also, the betaines reacted with methyl iodide to give imidazo-thiazolium salts which were unstable at high temperature and converted the quaternary ammonium salts of original biheterocycles.