• Proceedings of the Membrane Society of Korea Conference
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• 2001.05a
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• pp.108-111
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• 2001

• Proceedings of the Membrane Society of Korea Conference
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• 2003.11a
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• pp.210-213
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• 2003

• Proceedings of the Membrane Society of Korea Conference
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• 2001.04a
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• pp.41-47
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• 2001

• Proceedings of the Membrane Society of Korea Conference
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• 2000.04a
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• pp.38-42
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• 2000

• Membrane Journal
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• v.33 no.2
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• pp.77-86
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• 2023

In this study, pore-filled ion exchange membranes with low membrane resistance and high hydroxide ion conductivity was developed. To improve alkali durability, a porous substrate made of polytetrafluoroethylene was used, and a copolymer was prepared using monomers 2-(dimethyl amino) ethyl methacrylate (DMAEMA) and vinyl benzyl chloride (VBC) for pores. divinyl benzene (DVB) was used as the cross-linker, and ion exchange membranes were prepared for each cross-linking agent content to study the effect of the cross-linker content on DMAEMA-DVB and VBC-DMAEMA-DVB copolymers. As a result, chemical stability is improved by using a PTFE material substrate, and productivity can be increased by enabling fast photo polymerization at a low temperature by using a low-pressure UV lamp. To confirm the physical and chemical stability of the ion exchange membrane required for an anion exchange membrane fuel cell, tensile strength, and alkali resistance tests were conducted. As a result, as the cross-linking degree increased, the tensile strength increased by approximately 40 MPa, and finally, through the silver conductivity and alkali resistance tests, it was confirmed that the alkaline stability increased as the cross-linking agent increased.

• Membrane Journal
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• v.12 no.4
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• pp.247-254
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• 2002

In order to develop the ion exchange membranes which would be used in direct methanol fuel cell (DMFC), the polysulfone polymer was sulfonated using chlorosulfonic acid (CSA) and trimethylchlorosilane(TMCS). It has been characterized in terms of ion conductivities, methanol crossover, swelling degree and ion exchange capacities for the heat untreated and treated membranes at $150^{\circ}C.$ Typically, the methanol permeability and ion conductivity at the mole ratio of 1.4 between polysulfone repeating unit and sulfonating agents showed $2.87{\times}10^{-7}\; cm^2/s$(without heat treatment), $1.52{\times}10^{-7}\; cm^2/s$(with heat treatment) and $1.10{\times}10^{-2}\; S/cm$(without heat treatment), $0.87{\times}10^{-2}\;$ S/cm(with heat treatment), respectively. After the mole ration of 1.4 both values indicated mild increase.

• Membrane Journal
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• v.28 no.5
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• pp.326-331
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• 2018

Crosslinking of poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) anion exchange membranes, which can be used for capacitive deionization (CDI), was investigated. PPO Anion exchange polymer was prepared through bromination and amination reaction steps and crosslinked with bisphenol A diglycidylether (BADGE), m-phenylenediamine (m-PDA), and hexamethylenediamine (HMDA). The gelation time by crosslinking was short in the order of HMDA > m-PDA > BADGE. The anion exchange membranes crosslinked at room temperature over a certain amount of crosslinking agent did not dissolve in an aprotic solvent such as 1-methylpyrrolidone (NMP) and the chemical durability of their membranes to organic solvent increased. The ion exchange capacity and water uptake of anion exchange membranes crosslinked with different crosslinker (BADGE) contents were measured and compared. The CDI performance of the crosslinked PPO anion exchange membrane immersed in the HMDA solution was almost the same as that of the non - crosslinked membrane except for the initial stage of the adsorption step.

• Membrane Journal
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• v.27 no.2
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• pp.129-137
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• 2017

In this study, we have developed cation-exchange membranes (CEMs) which can efficiently separate heavy-metal ions among the cations contained in a water system. Sulfonated polyetheretherketone (SPEEK) was used as a base polymer and a powdered chelating resin with strong binding ability to heavy-metal ions was added into it. In order to optimize the performance of the CEM, the content of chelating resin powder and the ion exchange capacity of SPEEK have been controlled. As a result, it was confirmed that the removal efficiency of heavy metal ion was improved by more than 20% by applying the CEM to membrane capacitive deionization (MCDI).

• Membrane Journal
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• v.25 no.2
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• pp.144-151
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• 2015

The water-soluble poly(vinyl alcohol) membranes with the addition of sulfosuccinic acid (SSA) were prepared and to assign the ion exchange capacity, poly(4-styrene sulfonic acid-co-maleic acid) (PSSA_MA) was added to PVA according to PSSA_MA contents of 70, 80 and 90 wt%. To characterize the resulting membranes, FT-IR, water contents, ion exchange capacity, proton conductivity and methanol permeability were measured. As PSSA_MA contents increased, water contents, ion exchange capacity, proton conductivity increased, but methanol permeability decreased. From these results, the best preparation component was known as PVA10/SSA9/PSSA_MA80.

• Membrane Journal
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• v.20 no.4
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• pp.335-341
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• 2010

This study focuses on the investigation of the anion exchange membrane through blending poly(ethylenimine) (PEI) and poly(vinyl alcohol) (PVA) varying the mixing ratio. To characterize the resulting membranes, the water content, contact angle, FT-IR, thermal gravimetric analysis, ion exchange capacity, ion conductivity and elastic modulus were measured. The PVA / PEI = 90 / 10 membrane showed the ion conductivity, $5.16{\times}10^{-2}S/cm$ and simultaneously the contact angle, $78.3^{\circ}$. According to TGA measurement, the resulting membranes seemed durable at room temperature. Through the modulus test, the mechanical properties increased with increasing PVA content and apparently the membranes looked very robust.