• Polymer Science and Technology
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• v.2 no.2
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• pp.81-87
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• 1991

• Polymer Science and Technology
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• v.5 no.2
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• pp.115-123
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• 1994

• Polymer Science and Technology
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• v.7 no.2
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• pp.148-154
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• 1996

• Polymer Science and Technology
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• v.22 no.6
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• pp.553-560
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• 2011

• Polymer(Korea)
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• v.33 no.3
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• pp.268-271
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• 2009

In this study, the distribution behaviors of the polystyrene sulfonic acid (PSSA) grafting polymer across the FEP-g-PSSA membranes prepared by a simultaneous irradiation method, were investigated by analyzing the cross-section of the membranes with a SEM-EDX instrument. The effects of irradiation conditions such as the degree of grafting, FEP film thickness, and grafting solvent on the distribution of the grafting polymer were mainly studied in this experiment. The results indicate that to obtain the evenly grafted FEP-g-PSSA membranes, the higher degree of grafting is required as the film thickness increases, and the lower dose rate are more effective than the higher dose rate at the given dose.

• Journal of the Korean Electrochemical Society
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• v.9 no.2
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• pp.89-94
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• 2006

Nafion/poly(ether(amino sulfone)) acid-base blend polymer electrolyte membranes were prepared and their proton conductivity and dimethyl ether permeability were investigated. Characteristics of direct dimethyl ether fuel cell (DDMEFC) performance using prepared blend membrane were studied. The increase of amine groups in the base polymer in composite membranes resulted in the decrease in dimethyl ether permeability. The proton conductivity of the blend membranes gradually increased as increasing temperature. The conductivity of Nafion/PEAS-0.6 (85:15) blend membranes was measured to be $1.42\times10^{-2}S/cm\;at\;120^{\circ}C$ which was higher than that of the recast Nafion. The performance of direct dimethyl ether fuel cell (DDMEFC) using the Nafion/PEAS blend membranes was higher than that using $Nafion^(R)115$ membrane. Enhanced performance of direct dimethyl ether fuel cells using Nafion/PEAS blend membrane was explained by reducing dimethyl ether (DME) crossover through the electrolyte membrane and maintenance of the proton conductivity at high temperature.

• Proceedings of the Membrane Society of Korea Conference
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• 2005.05a
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• pp.93-94
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• 2005

• Applied Chemistry for Engineering
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• v.26 no.3
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• pp.326-330
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• 2015

Polymeric membranes have been used in various applications and generally applied to the systems prevented from exterior exposure. However, polymer membranes for outdoor usages such as, an air quality monitoring and membrane reservoirs for the selective recovery of useful metals from seawater, have been newly developed. Thus it is required to investigate the properties of the membrane for the outdoor use and also studies of the accelerated UV exposure onto the polymeric membranes are essential to estimate their weatherability. Herein, we report on the thermal and mechanical properties, morphology changes, and color differences of the polysulfone anisotropic membranes and non-woven type polypropylene membranes with the accelerated UV exposure. Results showed that the effect of UV exposure on the membrane depend not only on the polymer used but also on the form of the membrane. This work can provide some of key informations of the membrane for outdoor use.

• Membrane Journal
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• v.25 no.1
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• pp.32-41
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• 2015

High performance polysulfone microfiltration membranes with a high were successfully prepared by vapor induced phase separation (VIPS) coupled with non-solvent induced phase separation (NIPS) process. Asymmetric Membranes were prepared with PSF/DMF/PVP/PEG/DMSO/water mixed solutions and water/IPA coagulant. PSF, DMF, PVP, PEG, DMSO, water was used as a membrane polymer, a solvent, a hydrophilic polymer additive, a polar protic liquid polymer, a polar aprotic nonsolvent, and a polar protic nonsolvent in the casting solution, respectively. The addition of polar aprotic nonsolvents, and polar protic nonsolvents is a convenient and effective method to control membrane structure. In order to control the morphology of polymeric membranes, the spontaneous emulsification induced by drawing water vapor into the exposed casting solution surface has been used. Control of the internal morphology of polymeric membranes by using mixed coagulation solution such as water and IPA is discussed in the present work. The pure water permeability, pore size distribution, surface hydrophilicity and membrane morphology were investigated. Due to the addition of DMSO to casting solution, the mean pore size increased almost $0.2{\mu}m$ and the water flux increased about 1000-1800 LMH.

• Membrane Journal
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• v.25 no.2
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• pp.152-161
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• 2015

In this study, novel pore-filled anion-exchange membranes (PFAEMs) with low electrical resistance, high permselectivity, and low water-splitting flux property under a concentration polarization condition have been developed for the enhancement in the efficiency of electrochemical water treatment processes. The base membranes have been prepared by filling a copolymer containing quaternary ammonium groups with an excellent ion-exchange capability into a porous polyolefin substrate, showing a high performance superior to that of a commercial membrane. In addition, it was confirmed that the electrochemical membrane performances are preserved while the water-splitting flux is effectively controlled by coating an imidazolium polymer onto the surface of the base membrane. The prepared PFAEMs revealed remarkably low electrical resistances of about 1/6~1/8 compared to those of a commercial membrane, and simultaneously low water-splitting flux comparable with that of cation-exchange membranes under a concentration polarization condition.