• Proceedings of the Membrane Society of Korea Conference
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• 1995.10a
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• pp.33-35
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• 1995

현재 국내에서 생산되는 에탄올은 원료나 연료용으로 사용되는 합성알콜과 주류의 원료로 사용되는 발효알콜이 대부분을 차지하고 있다. 그러나 휘발유 첨가제, 연료용 알콜의 수요가 늘어날 경우 발효공정을 이용한 에탄올 연료의 사용이 늘어날 전망이며 특히 기존의 휘발유 첨가제 중 옥탄가 향상을 위한 MTBE 대신 에탄올, ETBE의 사용이 환경적인 측면이나 경제적으로 유리하다. 연로나 첨가제로서 에탄올을 사용하기 위해서는 기존의 95%의 순도를 갖는 일반에탄ㅇ올 대신에 99.5wt%이상의 고순도 에탄올을 생산하여야 하며 에탄올 농축공정 중의 하나인 Pervaporation은 국내에서 1-2년 전부터 연구가 활발히 진행되고 있으나 현재 국내에서 진행되고 있는 Pervaporation Test는 대부분 합성알콜을 이용하여 수행되었다. 이 실험에서는 주정공장에서 제조한 주정과 조주정을 이용, 현장 Pilot Test를 통해 PV System의 성능 검증, 에탄올 내 Trace 물질파악 및 필요 막면적을 이용하여 합성알콜과의 Performance비교를 수행하였다.

• 한국신재생에너지학회:학술대회논문집
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• 2006.06a
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• pp.77-80
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• 2006

Chloromethylated polysulfone(CMPSf) and a number of mono- and diamine compounds were used to prepare anion-exchange membranes(AEMs) and an ionomer binder solution. The properties of the AEMs were investigated such as $OH^-$ conductivity, water content and dimension stability. Chloromethylation and amination of PSf were optimized in terms of the properties. Membrane-electrode assemblies were fabricated using anion-exchange membranes and the ionomer binder for solid alkaline fuel cells and direct borohydride fuel cells.

• Membrane Journal
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• v.10 no.3
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• pp.103-111
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• 2000

• Proceedings of the Membrane Society of Korea Conference
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• 2004.07a
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• pp.167-215
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• 2004

• Korean Chemical Engineering Research
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• v.55 no.4
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• pp.473-477
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• 2017

The polymer membrane of proton exchange membrane fuel cell (PEMFC) has a great influence on PEMFC performance and durability. In this study, hydrogen permeability, fluorine emission rate (FER), lifetime, and performance of Nafion membranes with different thicknesses were measured to investigate the effect of thickness of polymer membrane on performance and durability. The relationship between membrane thickness and lifetime was obtained from the relationships between hydrogen permeability and membrane thickness, hydrogen permeability and FER, FER and lifetime. As the membrane became thicker, the hydrogen permeability and FER decreased and the lifetime increased. On the other hand, the performance decreased with increasing membrane resistance. The membrane thickness range satisfying both performance and durability was 25 to $28{\mu}m$.

• Korean Chemical Engineering Research
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• v.53 no.6
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• pp.690-694
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• 2015

Recently, direct formic acid fuel cells (DFAFC) among direct liquid fuel cells is studied actively. Economical hydrocarbon membranes alternative to fluorinated membranes for DFAFC's membrane are receiving attention. In this study, characteristics of sulfonated poly(ether ether ketone, sPEEK) and sulfonated poly(arylene ether sulfone, PAES) membranes were compared with Nafion membrane at DFAFC operation condition. Formic acid crossover current density of hydrocarbon membranes were lower than that of Nafion 211 fluorinated membrane. I-V performance of sPEEK MEA(Membrane and Electrode Assembly) was similar to that of Nafion 211 MEA due to similar membrane resistance each other. sPEEK MEA with low formic acid crossover showed higher stability compared with Nafion 211 MEA.

• Membrane Journal
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• v.26 no.5
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• pp.329-336
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• 2016

Proton exchange membrane (PEM) is one of the key components of membrane-electrode assembly (MEA), which plays important role in fuel cell performance together with catalysts. It is widely accepted that water channel morphology inside PEMs as a proton pathway significantly affects the PEM performance. Molecular dynamics (MD) simulations are a very useful tool to understand molecular and atomic structures of materials, so that many related researches are currently being studied. In this paper, we summarize the current research trend in MD simulations, present which properties can be characterized, and finally introduce the usefulness of MD simulations to the researchers for proton exchange membranes.

• Journal of the Korean Electrochemical Society
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• v.6 no.1
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• pp.68-71
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• 2003

The performance of the Direct Methanol Fuel Cell (DMFC) using multi-layer electrode, which prepared by various anode catalysts and Nafion membranes, was studied for reducing the amount of the metal catalyst loaded in the MEA system. The amount of the catalyst used in this experiment was $3-4 mg/cm^2$ in cathode and $1-2 mg/cm^2$ in anode, respectively. The best performance was to be $230 mS/cm^2$ of MEA3 at $90^{\circ}C$ and 2 bar in this experiment. However, the overall performance of the DMFC was maintained almost the same compared to the general commercial catalyst systems.

• Resources Recycling
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• v.20 no.4
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• pp.52-57
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• 2011

Present paper reports a new method to separate the electrolyte membranes and carbon paper without using ultrasonic waves and stirring. In this method, these were separated from fuel cell membrane-electrode assembly(MEA) using the distilled water, butanol and surfactant by dipping method without the dispersion of catalyst particles. Separated carbon paper catalysts and fuel cell Pt/C catalysts were heated in aqua regia at $80{\sim}85^{\circ}C$ and added to precipitant. After calcination, Pt metal was recovered which might be used in fabricating new fuel cells.

• Korean Chemical Engineering Research
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• v.52 no.6
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• pp.695-700
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• 2014

Proton Exchange Membrane Fuel Cells (PEMFC) can generate hydrogen and oxygen from water by electrolysis. But the electrode and polymer electrolyte membrane degrade rapidly during PEM water electrolysis because of high operation voltage over 1.7V. In order to reduce the rate of anode electrode degradation, unsupported $IrO_2$ catalyst was used generally. In this study, Pt/C catalyst for PEMFC was used as a water electrolysis catalyst, and then the degradation of catalyst and membrane were analysed. After water electrolysis reaction in the voltage range from 1.8V to 2.0V, I-V curves, impedance spectra, cyclic voltammograms and linear sweep voltammetry (LSV) were measured at PEMFC operation condition. The degradation rate of electrode and membrane increased as the voltage of water electrolysis increased. The hydrogen yield was 88 % during water electrolysis for 1 min at 2.0V, the performance at 0.6V decreased to 49% due to degradation of membrane and electrode assembly.