• Proceedings of the Membrane Society of Korea Conference
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• 1998.10a
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• pp.123-126
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• 1998

1960년 Allcock이 공기중에서 안정한 포스파젠고분자를 합성한 이래 포스파젠고분자는 열적, 화학적 안정성, 그리고 -P=N-골격에 다양한 측쇄를 부착함으로써 화학적으로 쉽게 고분자를 변형시킬 수 있다는 특징으로 인하여 이온교환막을 위한 기본고분자로 많은 관심을 끌고 있다. 1986년 MaCaffery등은 trifluoro- ethoxy를 치환한 고분자막을 합성하여 고온 안정성에 대한 특성을 실험한 바 있으며 1989년 Allen과 Macffrey등은 bistrifluoroethoxy를 치환시킨 포스파젠고분자를 합성하여 Co와 Mn이 들어있는 용액으로부터 Cr을 분리하였다. 그러나 trifluoroethoxy가 치환된 막은 소수성의 특징을 보이기 때문에 친수성이 요하는 곳에의 응용에는 사용할 수가 없었다. 친수성 포스파젠고분자의 합성의 경우는 1988년 Allcock과 Kwon등이 방사선을 이용하여 가교결합시켜 물에 녹지 않는 포스파젠 친수성 겔을 합성한 바 있으며 1990년 Wycisk등은 포스파젠 고분자를 슬폰화시켜 친수성을 가진 이온교환막을 합성하였다.

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2005.06a
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• pp.101-109
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• 2005

In order to produce only a pH-controlled solution without discharging any unused solution, this work has developed a continuous electrolytic system with a pH-adjustment reservoir being placed before an ion exchange membrane-equipped electrolyzer, where as a target solution was fed into the pH-adjustment reservoir, some portion of the solution in the pH-adjustment reservoir was circulated through the cathodic or anodic chamber of the electrolyzer depending on the type of the ion exchange membrane used, and some other portion of the solution in the pH-adjustment reservoir was discharged from the electrolytic system through other counter chamber with its pH being controlled as acid or base. The phenomena of the pH being controlled in the system could be explained by the electro-migration of the ion species in the solution through the ion exchange membrane under a cell potential difference between anode and cathode and its consequently-occurring non-charge equilibriums and electrolytic water- split reactions in the anodic and cathodic chambers.

• Membrane Journal
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• v.14 no.1
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• pp.44-52
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• 2004

This paper concerns the development of a cationic polymeric membranes for direct methanol fuel cell. The crosslinked poly(vinyl alcohol) (PVA) membranes with poly(acrylic acid-co-maleic acid) (PAM) and hydroquinonesulfonic acid (HQSA) as the crosslinking agents were prepared according to the amount of crosslinking agents. The resulting membranes were characterized in terms of methanol permeability, proton conductivity, water content and ion exchange capacity. The methanol permeability and proton conductivity increased with increasing PAM content up to 9 wt% and then decreased. This trend is considered the effect of the cross linking rather than the introduction of hydrophilic groups. When the HQSA contents were varied, no interesting increases of proton conductivity, water content and ion exchange capacity were found.

• Proceedings of the Membrane Society of Korea Conference
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• 2003.11a
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• pp.103-106
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• 2003

• Membrane Journal
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• v.32 no.5
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• pp.336-347
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• 2022

Reverse electrodialysis (RED) is one of the promising eco-friendly renewable energy technologies which can generate electricity from the concentration difference between seawater and freshwater by using ion-exchange membranes as a diaphragm. The ion-exchange membrane is a key component that determines the performance of RED, and must satisfy requirements such as low electrical resistance, high permselectivity, excellent durability, and low manufacturing cost. In this study, pore-filled anion-exchange membranes were fabricated using porous polymer substrates having various thicknesses and porosity, and the effects of ion-exchange polymer composition and membrane thickness on the power generation performance of RED were investigated. When the electrical resistance of the ion-exchange membrane is sufficiently low, it can be confirmed that the RED power generation performance is mainly influenced by the apparent permselectivity of the membrane. In addition, it was confirmed that the apparent permselectivity of the membranes can be improved through IEC, crosslinking degree, membrane thickness, surface modification, etc., and the optimum condition must be found in consideration of the trade-off relationship with electrical resistance.

• Membrane Journal
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• v.31 no.6
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• pp.371-383
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• 2021

Anion exchange membranes have been used for water electrolysis, which can produce hydrogen, and fuel cells, which can generate electrical energy using hydrogen fuel. Anion exchange membranes operate based on hydroxide ion (OH^-) conduction under alkaline conditions. However, since the anion exchange membrane shows relatively low ion conductivity and alkaline stability, there is still a limit to its commercialization in water electrolysis and fuel cells. To address these issues, it is important to develop novel anion exchange membrane materials by rationally designing a polymer structure. In particular, the polymer structure and synthetic method need to be controlled. By doing so, for polymers, the physical properties, ionic conductivity, and alkaline stability can be maintained. Among many anion exchange membranes, poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) is commercially available and easily accessible. In addition, the PPO has relatively high mechanical and chemical stability compared to other polymers. In this review, we introduce the recent development strategy and characteristics of PPO-based polymer materials used in anion exchange membranes.

• Journal of the Korean Electrochemical Society
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• v.19 no.1
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• pp.14-20
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• 2016

Vanadium redox flow battery (VRFB) is an energy conversion device in which charging and discharging are alternatively carried out by oxidation and reduction reactions of vanadium ions with different oxidation states. VRFB consists of electrolyte, electrode, ion-exchange membrane, etc. The role of ion-exchange membranes in VRFB separates anolyte and catholyte and provides a high conductivity to hydrogen ions. Recently much attention has been devoted to develop ideal ion-exchange membranes for VRFB. A number of developed ion-exchange membranes should be evaluated to find out ideal ion-exchange membranes for VRFB. Long-term durability test is a crucial characterization of ion-exchange membranes for commercialization, but is very time-consuming. In this study, the life time prediction protocol of ion-exchange membranes in VRFB cell tests was developed through short-term single cell performance evaluation (real total operation time, 87.5 hrs) at three different current densities. We confirmed a decrease in test time up to 96.2% of real durability tests (expected total operation time, 2,296 hrs) and 5~6% of relative error discrepancy between the predicted and the real life time in a unit cell.

• Membrane Journal
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• v.7 no.3
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• pp.136-141
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• 1997

Humic acid has been extracted and purified from biologically nondegradable humic substances. Using the ion exchange capability of carboxylic acids which are the main component of the humic acids, a membrane was prepared with poly(viny1 alcohol). Its transport behavior of biologically active ions, $K^+$and $Na^+$, were investigated. The ion transport velocity increased with hydrogen ion concentration, especially, in the range of $10^-1$~$10^0$. The selectivity increased with increasing the concentrations of $K^{＋}$ and Na$^{＋}$, In particular, the transport velocity of $K^+$ increased twice compared to that of $Na^+$ at the 100 hydrogen ion concentration. In this regards, humic acid may be used as a new material for ion exchange membranes.

• Transactions of the Korean Society of Mechanical Engineers B
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• v.38 no.5
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• pp.437-441
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• 2014

This paper presents a novel microplatform for high power generation based on reverse electrodialysis. The ideal cation-selective membrane for power generation was realized using geometrically controlled in situ self-assembled nanoparticles. Our proposed membranes can be constructed through a simple and cost-effective process that uses microdroplet control with nanoparticles in a microchannel. Another advantage of our system is that the maximum power and energy conversion efficiency can be improved by changing the geometry of the microchannel and proper selection of the nanoparticle size and material. This proposed platform can be used to supply power sources to other microdevices and contribute to a fundamental understanding of ion transport behavior and the power generation mechanism.

• Membrane Journal
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• v.27 no.3
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• pp.240-247
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• 2017

In this study, the heterogeneous ion exchange membranes prepared by the combination of the carbon electrode and mixed the cation and anion exchange polymers and polyvinylidene fluoride as the basic polymer together were made to recognize the efficiency of the salt removal for the application of the membrane capacitive deionization process. The mixing weight ratio of the solvent, basic polymer and ion exchange resin was 7 : 2 : 1 and this mixed solution was directly cast on the electrode. As for the operating conditions of the adsorption voltage and time, feed flow rate, desorption voltage and time of the feed solution NaCl 100 mg/L, the salt removal efficiencies (SRE) were measured. Apart from this NaCl, the $CaCl_2$ and $MgSO_4$ solutions were investigated in terms of SRE as well. Typically, SRE for NaCl 100 mg/L solution under the conditions of adsorption voltage/time, 1.5 V/3 min, desorption voltage/time -0.1 V/3 min, was shown 98%. And for the $CaCl_2$ and $MgSO_4$ solutions, the SREs of 70 and 59% were measured under the conditions of adsorption voltage/time, 1.2 V/3 min, desorption voltage/time -0.5 V/5 min, respectively.