• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1994년도 추계학술대회 논문집
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• pp.198-201
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• 1994

Stability improvement of fragile LB films was attempted by polyion complexation of monolayers at the air-water interface and crosslinking of the resulting LB films. The spreading polymers were synthesized by radical copolymerization of monoalkyl itaconate with oligoethyleneglycol methyl vinylether, and poly(allylamine) was employed as the subphase polymer. Formation and characteristic of the monolayers were comfirmed by surface pressure-area($\pi$-A) isotherms. The two different polymers formed polyion-complexed monolayer through the formation of carboxylate/ammonium salt at the air-water interface. Y-type deposition occurred on solid substrates, and the transfer ratio was over 0.7. Pores (diameter, 0.1$\mu\textrm{m}$) of a membrane filter could be covered by polyion-complexed 6 layers. Interactions of the polymers with metal ions were investigated of the air-water interface and in the LB films. The structure change and macroscope morphology of the LB films were confirmed by FT-lR and SEM, respective1y.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2009년도 추계학술대회 논문집
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• pp.150-153
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• 2009

Anion exchange polymer electrolyte pore-filling membranes consisting of the whole hydrocarbon materials were prepared by photo polymerization with various quaternary ammonium cationic monomers and characterized on the properties for applying to solid alkali fuel cell (SAFC). Hydrocarbon porous substrates such as polyethylene were used for the preparation of the pore-filling membranes. The hydroxyl ion conductivity of the polymer electrolyte membranes prepared in this research was dependent on the composition ratio of an electrolyte monomer and crosslinking agents used for polymerization. Furthermore, these pore-filling membranes have commonly excellent properties such as smaller dimensional affects when swollen in solvents, higher mechanical strength, lower fuel crossover through the membranes, and easier preparation process than those of traditional cast membranes.

• Elastomers and Composites
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• 제29권2호
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• pp.121-130
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• 1994

The physical properties of rubber blend between natural rubber(NR) and ethylene propylene diene terpolymer(EPDM) were investigated as a study of EPDM composite materials. For EPDM/NR blends, the effects of ethylene and diene contents in EPDM, blend ratio, dicumyl peroxide(DCP) curing system on the physical properties, interfacial adhesion force and dynamic crack growth etc. were studied. EPDM/NR blends loaded with carbon black were prepared by mechanical mixing and cured by plate heating cure press. Crosslinking density was measured by swelling method with toluene. The physical properties of all blends were measured with Instron, fatigue to failure(FTF), Demattia flex cracking tester(DMFC), scanning electron microscopy (SEM), etc. As the ethylene and diene contents in EPDM increased, the physical properties, such as dynamic crack growth, adhesion to other component were increased too. Interfacial adhesion force of EPDM/NR blends to dissimilar layer was improved by the use of optimum peroxide curing system.

• Korean Membrane Journal
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• 제1권1호
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• pp.73-80
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• 1999

The removal of trace chlorinated and aromatic hydrocarbons from water by a pervaporation technique has been carried out through poly (dimethylsiloxane) membrane which had been fabricated by the addition crosslinking reaction. This study dealt with the swelling and permeation behaviors of the PDMS membranes with dichloroethane trichloroethane and toluene aqueous solutions. The swelling ratio in the toluene aqueous solution was much higher than those in the chloroethane solutions at all of the operating temperatures and concentrations. The solubility parameter theory was introduced to interpret the affinity between permeates and a membrane material and in all cases this approach seemed to be proper. It was suggested that the existence of water clusters in the membrane due to the hydrophobic characteristics of the membrane made the size of the permeating water larger resulting in suppressing water permeation and increasing enrichment of the organic components. The permeation behaviors at different membrane thicknesses were indirectly interpreted in terms of the effect of concentration polarization.

• Elastomers and Composites
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• 제53권3호
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• pp.136-140
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• 2018

In this study, research was conducted into the manufacture of thermally expandable microspheres for automotive underbody coatings and applications in industry. In particular, the relationship between heat resistance and the ratio of crosslinking agents and initiators in the manufacture of the thermally expandable microspheres was investigated. We focused on the results with various cross-linking agents; our aim was to make the walls of the microspheres thicker to solve the problem of reductions in size caused by shrinkage when the microspheres are heated to $T_m$ ($T_{max}$). We observed the sectional thickness and surface of the samples with thicker walls. The thick thermally expandable microspheres showed reduced shrinkage and excellent stability in spite of prolonged exposure to heat.

• 한국응용과학기술학회지
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• 제36권2호
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• pp.645-655
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• 2019

본 연구에서는 강도를 조절한 마이크로겔을 사용하여 다양한 점탄성을 갖는 콜로이드 마이크로겔을 제조하였다. 하이드로겔의 화학적 가교제의 함량이 증가할수록 팽윤비는 $2.0{\times}10^4%$에서 $6.0{\times}10^3%$까지 감소하였고, 강도는 22.2 kPa에서 99.7 kPa까지 증가하였다. 이를 $100{\mu}m$ 크기로 분쇄하여 마이크로겔을 제작하였고 이온성 가교결합을 유도하는 분산액과 혼합하여 콜로이드 마이크로겔을 제작하였다. 그 결과, 가교제의 가교도와 분산액에 따라 $10^{-1}rad/s$의 진동수에서 1.679 kPa.s에서 86.485 kPa.s까지 점도를 세밀하게 조절할 수 있었다. 본 연구에서는 콜로이드 마이크로겔의 물성을 제어하기 위해 하이드로겔의 가교도를 조절 또는 분산액의 종류와 함량을 조절하여 다양한 유변학적 거동을 갖는 콜로이드 마이크로겔을 제조하였다. 물성을 제어할 수 있는 콜로이드 마이크로겔을 사용하여 향후 콜로이드 현탁액 및 유화를 제조하는 화장품, 제약, 페인트 및 식품 산업에서 목적에 따라 적합한 물성을 갖는 콜로이드 마이크로겔을 제조할 수 있다.

• 폴리머
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• 제32권4호
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• pp.390-396
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• 2008

조직공학용 생체재료로 사용하고자 가교제 1,3-butadiene diepoxide(BD)를 사용하여 락타이드(LA)와 가교시킨 히아루론산(HA) 고분자를 제조하였다. 가교된 고분자의 락타이드 및 BD 반응도는 핵자기 공명 분광법으로 결정하였다. 반응도와 팽윤도는 LA/HA 몰비 혹은 가교제 농도를 증가시킴에 따라 증가하였다. 탄성률은 가교제 농도가 증가하거나 HA/LA 몰비가 감소함에 따라 감소하였다. 생분해는 2단계로 진행되었으며 BD 농도가 증가할수록 서서히 진행되었다. 첫 단계 분해는 주로 가교구조에 존재하는 에스테르기의 분해에 기인한 것으로 나타났다. 세포 성장 저해는 BD 농도가 증가함에 따라 증가하였다. 세포 독성은 BD 농도가 클 경우 약간 나타났으나 그 값은 6% 미만으로 세포 성장에 큰 문제는 없는 것으로 나타났다.

• Macromolecular Research
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• 제15권4호
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• pp.363-369
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• 2007

Novel biodegradable elastic hydrogels, based on hydrophilic and hydrophobic polymer blocks, were synthesized via the radical crosslinking reaction of diacrylates of poly(ethylene glycol) (PEG) and poly(${\varepsilon}-caprolactone$) (PCL). PEG and PCL diols were diacrylated with acryloyl chloride in the presence of triethylamine, with the reaction confirmed by FT-IR and $^1H-NMR$ measurements. The diacrylate polymers were used as building-blocks for the syntheses of a series of hydro gels, with different block compositions, by simply varying the feed ratios and molecular weights of the block components. The swelling ratio of the hydrogels was controlled by the balance between the hydrophilic and hydrophobic polymer blocks. Usually, the swelling ratio increases with increasing PEG content and decreasing block length within the network structure. The hydrogels exhibited negative thermo-sensitive swelling behavior due to the coexistence of hydrophilic and hydrophobic polymer components in their network structure, and such thermo-responsive swelling/deswelling behavior could be repeated using a temperature cycle, without any significant change in the swelling ratio. In vitro degradation tests showed that degradation occurred over a 3 to 8 month period. Due to their biodegradability, biocompatibility, elasticity and functionality, these hydrogels could be utilized in various biomedical applications, such as tissue engineering and drug delivery systems.

• 유기물자원화
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• 제12권4호
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• pp.95-104
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• 2004

본 연구에서는 가연성 건설폐기물 재활용의 일환으로, 폐발포폴리스티렌의 스티렌 용액에 가교제 및 개시제를 첨가하여 제조한 결합재와, 폐목재 칩을 이용하여, 폐목재-플라스틱 복합패널을 제조하였다. 전열 프레스를 이용하여 다양한 결합재량 및 충전재-결합재 비를 갖는 복합패널 공시체를 제조하였으며, 그 겉보기 밀도, 흡수율, 흡수에 의한 팽창률, 휨강도, 내수성 등에 관한 일련의 실험을 행하였다. 폐목재-플라스틱 복합패널의 겉보기밀도는 결합재량 및 충전재-결합재비의 증가에 따라 증대하며, 그 휨강도 및 습윤 휨강도는, 결합재량 35%, 충전재-결합재비 0.8에 있어서 최대치에 이른다. 흡수율 및 흡수에 의한 두께 팽창률은, 결합재량 및 충전재-결합재비의 증가에 따라 현저하게 감소한다. 결합재량 30%이상의 경우, 충전재-결합재비에 관계없이, 복합패널의 24h 상온 수중($20^{\circ}C$) 침지 및 2h 끓는 물중($100^{\circ}C$)＋1h상온 수중($20^{\circ}C$) 침지에 의한 휨강도의 감소는 거의 발생하지 않으며, 높은 내수성을 발현한다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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• pp.129.2-129.2
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• 2010

AEM which were used for solid alkaline fuel cell(SAFC) were prepared by photo polymerization in method pore-filling with various quaternary ammonium cationic monomers and crosslinkers without an amination process. Their specific thermal and chemical properties were characterized through various analyses and the physico-chemical properties of the prepared electrolyte membranes such as swelling behavior, ion exchange capacity and ionic conductivity were also investigated in correlation with the electrolyte composition. The polymer electrolyte membranes prepared in this study have a very wide hydroxyl ion conductivity range of 0.01 - 0.45S/cm depending on the composition ratio of the electrolyte monomer and crosslinking agent used for polymerization. However, the hydroxyl ion conductivity of the membranes was relatively higher at the whole cases than those of commercial products such as A201 membrane of Tokuyama. These pore-filling membranes have also excellent properties such as smaller dimensional affects when swollen in solvents, higher mechanical strength, lowest electrolyte crossover through the membranes, and easier preparation process compared of traditional cast membranes. The prepared membranes were then applied to solid alkaline fuel cell and it was found comparable fuel cell performance to A201 membrane of Tokuyama.