• 전기학회논문지
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• 제59권12호
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• pp.2235-2239
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• 2010

In this study, The cation exchange membrane and the anion exchange membrane affect in electrical conduction of metal fuel cell was investigated. Magnesium material as anode electrode and the NaCl solution dissolved with 5~15wt% as electrolyte were used for the metal fuel cell. It was found that magnesium slag where flows toward the air electrode was suppressed by using ion exchange membrane. The open circuit voltage variation during discharge has very flat pattern by using ion exchange membrane, but the case which is not the exchange membrane, the open circuit voltage increased according to time. When using the anion exchange membrane, the electric current was higher case of the cation exchange membrane, as a result of higher equivalent conductivity in anion Cl-. The cation exchange membrane was observed with the fact that the output power is excellent in compared with anion exchange membrane.

• 폴리머
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• 제26권5호
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• pp.575-581
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• 2002

본 연구는 폴리에틸렌 기재에 비드와 섬유상 이온교환체의 배합비를 달리하여 불균질 이온 교환막을 제조하였다. PE 불균질 이온교환막의 이온교환능은 섬유강 이온교환체의 양이 증가할수록 선형적으로 증가하였으며 30 wt%에서 최대 1.86 meq/g 이었다. 불균질 이온교환막의 함수율, 고정이온농도 및 이온운반율도 섬유상 이온교환체의 양이 증가할수록 증가하였나. 반면 불균질 이온교환막의 전기저항은 섬유상 이온교환체의 양이 증가할수록 감소하였으며, IXF (ion exchange fiber)의 혼합량이 30 wt%에서 5$\Omega$/$\textrm{cm}^2$으로 전기저항 값이 가장낮았다.

• 멤브레인
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• 제10권2호
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• pp.66-74
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• 2000

In consideration that a high tensile strength and ion exchange capacity are maintained as the swelling of membrane is controlled by the coagulation of PSf with the introduction of ion exchange groups and PPSS without the introduction of ion exchange groups, the block copolymer of PSf and PPSS were synthesized. The cation exchange membrane was prepared by sulfonation with CSA and casted. The synthesized block copolymer and cation exchange membrane were characterized by FT-IR and their thermal stability was confirmed by TGA. The optimum sulfonation could be accomplished at a mole ratio of BPSf to CSA 1:3. The best electrochemical properties obtained by the optimal condition were area resistance of 4.37 $\Omega$ㆍ$\textrm{cm}^2$, ion exchange capacity of 1.71 meq/g dry membrane, water content of 0.2941 g $H_2O$/g dry membrane, and fixed ion concentration of 5.81 meq/g $H_2O$. When GBL was used as an additive, area resistance was increased by 13.7 % and ion exchange capacity was increased by 14.6%. When the membrane was fabricated in a form of composite using non woven cloth as a support. the tensile strength of membrane could be improved, but the electrochemical characteristics were not influenced.

• Membrane and Water Treatment
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• 제3권4호
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• pp.211-219
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• 2012

To enhance the efficiency of water treatment and reduce the extent of membrane fouling, the membrane separation process is frequently preceded by other physico-chemical processes. One of them might be ion exchange. The aim of this work was to compare the efficiency of natural organic matter removal achieved with various anion-exchange resins, and to verify their potential use in water treatment prior to the ultrafiltration process involving a ceramic membrane. The use of ion exchange prior to ceramic membrane ultrafiltration enhanced final water quality. The most effective was MIEX, which removed significant amounts of the VHA, SHA and CHA fractions. Separation of uncharged fractions was poor with all the resins examined. Water pretreatment involving an ion-exchange resin failed to reduce membrane fouling, which was higher than that observed in unpretreated water. This finding is to be attributed to the uncharged NOM fractions and small resin particles that persisted in the water.

• 환경위생공학
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• 제16권2호
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• pp.38-46
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• 2001

In this work, the heterogeneous ion exchange membrane was used in a electrodialysis apparatus to treat a Ni planting rinse water because the heterogeneous ion exchange membrane was excellent efficiency as compared with low manufacturing cost, was easy to make, and had a good mechanical properties. For a regeneration of membrane and to obtain the optimal condition for a scale-up of apparatus after treating Ni plating rinse water, we would find about the limiting current density and the concentration polarization. When the Ni plating rinse water 150mg/L was treated with the electrodialysis apparatus using the heterogeneous ion exchange membrane, the limiting current density was about $1.49{\;}mA/\textrm{cm}^2$. And the limiting current density increased with the flow rate and concentration of Ni plating rinse water. We recognized that the used membrane could be reused by periodic backwashing because efficiency was constant when the membrane was backwashed after treating wastewater.

• 제어로봇시스템학회:학술대회논문집
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• 제어로봇시스템학회 2004년도 ICCAS
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• pp.96-100
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• 2004

Ion exchange polymer membrane in the dehydrated state was found to exhibit bending upon a small applied voltage, although the investigations on the hydrated ion exchange polymer membrane bending behavior have been performed quite intensively for more than a decade for the purpose of producing a practical polymer actuator. Our investigation on the dehydrated ion exchange polymer membrane has revealed that its bending direction is perfectly controllable by the polarity control of applied voltage and the degree of its bending curvature is also almost completely determined by the control of duration time of voltage application on it, while the hydrated ion exchange polymer membranes lack of such properties. Furthermore the longevity of dehydrated ion exchange polymer membrane sustaining such a highly controllable properties has been found quite longer than that of the hydrated ion exchange polymer membrane.

• 멤브레인
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• 제33권3호
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• pp.137-147
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• 2023

본 연구에서는 현탁중합을 통해 이온교환입자를 합성하였다. 또한 음이온 교환막을 제조하기 위해 brominated poly(phenylene oxide) (Br-PPO)로 교환막 합성을 진행하였으며, 합성한 이온교환입자를 Br-PPO에 첨가하여 음이온 교환막에 성능을 향상시키고자 하였고, 이를 적용하여 음이온 교환막 연료전지 시스템의 성능 평가를 진행했다. 이온교환입자는 FT-IR, TGA 및 UTM을 통해 구조 분석, 열적 기계적 특성을 평가하였다. Br-PPO는 NMR을 통해 화학적 구조 분석 및 합성여부를 확인하였고, 음이온 교환막 연료 전지 셀 테스트를 진행하기 전 이온전도도와 이온교환용량, 팽윤도 및 수분함수율을 측정해 연구되고 있는 다른 음이온 교환막들과 비교를 통해 성능을 평가했다. 최종적으로 가장 성능이 우수했던 이온교환입자를 0.7 wt%를 첨가한 Br-PPO-TMA- SDV 음이온 교환막을 연료전지 시스템에 도입하여 상용 막인 FAA-3-50과 성능을 비교했다.

• 멤브레인
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• 제30권2호
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• pp.79-96
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• 2020

환경오염과 화석연료의 문제로 인한 2차 에너지 변환 및 저장 장치의 개발이 활발하게 진행되고 있다. 이러한 에너지 변환장치들은 전기화학적 시스템을 기본으로 운영되고 있으며 이온교환막은 각 공정의 성능을 결정짓는 중요한 요소이다. 따라서 에너지 시스템의 효율 증대 및 성능 향상을 위해서는 적합한 물성을 갖는 이온교환막 개발이 필요하다. 이러한 이온교환막은 크게 양이온교환막, 음이온교환막, 바이폴라막으로 분류되고 있으며, 이들 막들은 화학적, 물리적, 형태학적 특성에 따라 다양한 용도을 갖고 있다. 본 총설에서는 이온교환막의 주요한 특징과 함께 이들의 제조 방법에 대해 기술했다. 이어서 이온교환막을 이용하여 최근 개발되고 있는 전기화학 시스템에 기반을 둔 역전기 투석, 레독스 흐름 전지, 수전해 공정에 대해서 소개하고, 각 에너지 공정에서 이온교환막이 갖는 역할과 조건에 대해서 설명하였다.

• 멤브레인
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• 제27권2호
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• pp.109-120
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• 2017

양이온($Na^+$) 및 음이온($Cl^-$)이 각각의 CEM과 AEM을 통해 선택적으로 분리되어 담수로 이동할 때 발생되는 전위차와 산화/환원(redox couple)형 전해질을 포함하고 있는 전극에서 발생하는 전류를 이용하여 전기 에너지로 전환시키는 에너지변환장치이다. RED 시스템의 핵심소재 중 하나인 이온교환막은 높은 출력 밀도를 달성하기 위해 1) 낮은 팽윤거동, 2) 적절한 이온교환능, 3) 높은 이온전도도, 4) 높은 이온선택성을 만족시켜야 한다. 본 논문에서는 이를 만족시키는 소재 및 이온교환막의 연구동향 및 전망에 대해 설명하였다.

• Membrane and Water Treatment
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• 제3권1호
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• pp.63-76
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• 2012

Mother liquid discharged from a salt-manufacturing plant was electrodialyzed at 25 and $40^{\circ}C$ in a continuous process integrated with $SO_4{^{2-}}$ ion low-permeable anion-exchange membranes to remove $Na_2SO_4$ and recover NaCl in the mother liquid. Performance of electrodialysis was evaluated by measuring ion concentration in a concentrated solution, permselectivity coefficient of $SO_4{^{2-}}$ ions against $Cl^-$ ions, current efficiency, cell voltage, energy consumption to obtain one ton of NaCl and membrane pair characteristics. The permselectivity coefficient of $SO_4{^{2-}}$ ions against $Cl^-$ ions was low enough particularly at $40^{\circ}C$ and $SO_4{^{2-}}$ transport across anion-exchange membranes was prevented successfully. Applying the overall mass transport equation, $Cl^-$ ion and $SO_4{^{2-}}$ ion transport across anion-exchange membranes is evaluated. $SO_4{^{2-}}$ ion transport number is decreased due to the decrease of electro-migration of $SO_4{^{2-}}$ ions across the anion-exchange membranes. $SO_4{^{2-}}$ ion concentration in desalting cells becomes higher than that in concentration cells and $SO_4{^{2-}}$ ion diffusion is accelerated across the anion-exchange membranes from desalting cells toward concentrating cells.