• Elastomers and Composites
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• 제54권2호
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• pp.128-134
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• 2019

Many scientific approaches have been developed for the preparation of alternative crosslinker system of amino resins and isocyanate prepolymers. Herein, copolymerization of trimethoxy silane with N-butoxymethyl acrylamide was performed, and the product was reacted with hydroxyl groups in the alkyl main chain without the need for an additional crosslinker. For the crosslinker synthesized herein, the molecular weight, glass transition temperature, and viscosity increased with increasing content of N-butoxymethyl acrylamide.

• Bulletin of the Korean Chemical Society
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• 제1권4호
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• pp.138-143
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• 1980

Hydrogel membranes were prepared by copolymerizing 2-hydroxyethyl methacrylate (HEMA) and N-vinyl-2-pyrrolidone (VP) in the presence of the solvent and the crosslinker tetraethyleneglycol dimethacrylate (TEGDMA). By changing the monomer composition and the crosslinker content, different membranes were synthesized. Using these membranes, relative permeabilities and distribution coefficients for amides including urea were measured. The water contents in membrane were also measured. On the basis of solute-membrane matrix interaction, the results were interpreted.

• Journal of Applied Biological Chemistry
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• 제48권4호
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• pp.213-217
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• 2005

Microbial hydrogel was prepared with poly(${\gamma}$-glutamic acid) produced from Bacillus subtilis BS62 using crosslinking reagent, ethylene glycol diglycidyl ether (EGDE), and its physico-chemical characteristics were examined. Hydrogel which prepared from 10 grams of 10% PGA solution with $600\;{\mu}l$ of EGDE at $50^{\circ}C$ for 17 h swelled 4,320 times its dry weight, and time to reach swelling equilibrium in deionized water at 4 to $45^{\circ}C$ range was about 20 h. Swollen hydrogel shrunk in ionic solutions, and rate of shrinkage was higher in calcium chloride solution than sodium chloride solution. Swelling rate of hydrogel increased 1.3-fold of initial swelling rate for 30 min at $80^{\circ}C$.

• Bulletin of the Korean Chemical Society
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• 제19권11호
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• pp.1168-1171
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• 1998

Two kinds of second-order nonlinear optical copolymers were prepared by the copolymerization of the vinyl monomers containing NLO chromophore, methacrylic acid, and methyl methacrylate or butyl methacrylate. Glass transition temperatures (Tg of copolymers were around 130 ℃. The copolymers were soluble in common organic solvents such as tetrahydrofuran (THF), cyclohexanone, and N,N-dimethylformamide (DMF). The crosslinked copolymer was obtained by thermal treatment using pentaerythritol tetrakis(2-mercaptoacetate) as a crosslinker and became insoluble in tetrahydrofuran (THF) and N,N-dimethylformamide (DMF). Poling was carried out at 120 ℃ for 20 min and identified with UV-Vis spectroscopy. Electro-optic coefficient (r33) measurement showed a value of 35 pm/V for polymer 2 at 633 nm. Temporal stability of copolymers was improved owing to the crosslinked network, which was successfully obtained at 170 ℃ for 30 min after poling.

• 공업화학
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• 제20권2호
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• pp.195-200
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• 2009

폴리에스터계 분체도료용 경화제로 사용하기 위하여 상업용 ${\beta}-hydroxyalkylamide$ (${\beta}-HAA$)의 주사슬에 cyclohexane 고리가 도입된 $N^1,N^1,N^4,N^4$-tetrakis(hydroxyethyl)cyclohexane-1,4-dicarboxamide ($Cy-{\beta}-HAA$)를 dimethyl trans-1,4-cyclohexanedicarboxylate과diethanolamine로부터 높은 수율로 합성하고 NMR, MS 및 FT-IR 스펙트럼으로 구조를 확인하였다. 합성된 $Cy-{\beta}-HAA$는 기존의 ${\beta}-HAA$에 비하여 열적 안정성이 우수할 뿐만 아니라, 폴리에스터 분체 도료의 경화제로 사용했을 시 ${\beta}-HAA$를 사용한 것에 비해 더 매끄러운 도막이 형성되었으며 도막 표면에 핀홀(pinhole)의 생성이 감소되었다.

• Bulletin of the Korean Chemical Society
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• 제5권3호
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• pp.104-108
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• 1984

The self-diffusion experiment of THO was performed across a series of copolymer hydrogel membranes at different temperatures. Copolymer hydrogel membranes were prepared by copolymerizing 2-hydroxyethyl methacrylate (HEMA) and 2-aminoethyl methacrylate (AEMA) in the presence of the solvent and the crosslinker, ethylene glycol dimethacrylate (EGDMA). By changing the crosslinker content and the ratio of HEMA and AEMA monomer, two series of copolymer hydrogel membranes were synthesized. The tagging material was THO and efflux of THO was counted on a Liquid Sc-intillation Counter. The experimental data show that the permeability decreases as the amount of EGDMA and the mole fraction of HEMA increase, and the permeability is proportional to the temperature. The partition coefficient shows a parallel trend with permeability. Using the relationship between viscosity and diffusivity, the viscosity of water within the membrane was obtained. According to the result, the viscosity of watler within the membrane has the same value with those of supercooling water. And we obtained the activation energy of THO for transport in the membrane by using Arrhenius plotting.

• Macromolecular Research
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• 제17권10호
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• pp.734-738
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• 2009

Biodegradable, pH-sensitive, glycol chitosan (GC) hydrogels were prepared using divinyl adipate (DVA) as a crosslinker and acetic acid as a catalyst. DVA has highly reactive double vinyl ester groups and GC contains a high density of hydroxyl groups, with two in every glucosamine unit. The transesterification reaction between vinyl esters and hydroxyl groups produced crosslinked GC hydrogels. The initial crosslinking reaction was monitored by measuring the viscosity of the reaction mixture. When DVA was added to the GC solution and heated to $50^{\circ}C$, the viscosity of the GC solution gradually increased, implying a crosslinking reaction and hydrogel formation. A new peak from the ester group was observed in the FTIR spectra of the GC hydrogels, confirming the crosslinking reaction. The synthesized GC hydrogel showed pH-dependent water absorbency, mainly due to the presence of amine groups ($-NH_2$) at the C-2 position of the glucosamine unit of GC. The water absorbency greatly increased at acidic pH and slightly decreased at alkaline pH. The GC hydrogel gradually degraded in $37^{\circ}C$ water due to hydrolysis of the ester bonds, which were intermolecular crosslinking sites. A red dye, 5-carboxyltetramethyl-rhodamine (CTMR), was entrapped in the GC hydrogels as a model compound. CTMR was released from GC hydrogels in two steps: an initial burst release mainly due to desorption and diffusion, and a second sustained release possibly due to gradual degradation.

• 접착 및 계면
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• 제2권4호
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• pp.1-9
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• 2001

실리콘 실란트는 실리콘폴리머, 가소제(plasticizer), 가교제(crosslinker), 충전제(filler), 촉매(catalyst), 첨가제(additive) 등으로 제조할 수 있으며, 실란트의 실용특성에는 각 제조변수의 종류와 혼합비율이 크게 영향한다. 알코올형 실리콘 실란트는 최근들어 환경적인 이점 때문에 그 사용이 늘고 있다. 본 연구에서는 상온경화형 일액형 알코올형 실리콘 실란트를 PDMS(polydimethylsiloxane)의 점도를 달리하여 제조한 후 그 접착특성을 평가하였다. 또한 점도 20000과 80000 cps의 PDMS를 혼합 사용하고 가교제, 가소제, 촉매 등의 함량을 변화시켜가면서 실란트를 제조하고 접착특성을 평가하였다. 또한 각 실란트의 제조과정 중의 반응온도 변화를 기록하여 적절한 제조조건을 얻도록 하였다. 실란트 제조시 혼합물의 온도가 $40^{\circ}C$ 이하가 되도록 제조변수의 조성을 조절하여 적합한 물성의 실란트를 제조할 수 있었다. 피착재에 따라 접착력이 달라졌으며, 유리/유리 > 유리/알루미늄 > 알루미늄/알루미늄 순으로 나타났다. 실란트의 신장률은 폴리머 점도와 가소제의 함량 증가에 따라 증가하였으며, 강도는 가교제와 가소제 함량 감소와 촉매함량 증가에 따라 증가하였다.

• Elastomers and Composites
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• 제49권3호
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• pp.199-203
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• 2014

아크릴 단량체인 2-ethylhexyl acrylate (2-EHA), 2-hydroxyethyl acrylate (2-HEA), isobornyl acrylate (IBOA)를 광중합을 통하여 3원 공중합체 시럽을 합성하였다. 이관능기 아크릴 단량체인 1,6-hexanediol diacrylate (HDDA), poly(ethylene glycol) diacrylate (PEGDA, Mn = 250, 575, 700)를 가교제로 사용하여 semi-IPN형 감압성 점착제 (Pressure sensitive adhesives; PSAs)를 UV-광가교 시켜 제조하였다. 가교제 변화에 따른 감압성 점착제의 점착특성, 저장탄성율, 그리고 광학특성을 고찰하였으며, 점착특성과 저장탄성율은 가교제의 화학구조와 분자량에 의존하였다. 광학특성은 모든 감압성 점착제에서 92.5 % 이상의 광투과도 (at 550 nm), 1.0 % 이하의 haze값, 0.3 이하의 색차계값을 보임을 확인하였다. 결과적으로 가교제의 종류에 영향을 받지 않음을 확인하였다.

• Biomaterials and Biomechanics in Bioengineering
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• 제4권1호
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• pp.1-8
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• 2019

The aim of this study was to investigate the effect of total polymer concentration on the chemical structure, morphology of pores, porosity, swelling ratio, degradation of gelatin-poly (vinyl alcohol) (Gel-PVA) cryogel scaffolds. Porous cryogels were prepared with cryogelation technique by using glutaraldehyde as a crosslinker. Functional group composition of cryogels after crosslinking was investigated by Fourier Transform Infrared (FTIR). The morphology of cryogels was characterized via scanning electron microscopy (SEM) and porosity analysis. All of the cryogels had a porous structure with an average pore size between $45.58{\pm}14.28$ and $50.14{\pm}4.26{\mu}m$. The cryogels were biodegradable and started to degrade in 14 days. As the polymer concentration increased the swelling ratio, the porosity and the degradation rate decreased. Spongy and mechanically stable Gel-PVA cryogels, with tunable properties, can be potential candidates as scaffolds for tissue engineering applications.