• Membrane Journal
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• v.17 no.2
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• pp.118-123
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• 2007

Performances of fluoropolymers related to membranes manufacturing for different purposes are reviewed in the present article. In particular the main physical, mechanical and chemical properties of PVDF, ECTFE and PFSA ionomers are described in their specific applications. The excellent chemical resistance and suitable electrochemical properties make fluoropolymers an especially good choice in membranes manufacturing.

• Proceedings of the Korean Fiber Society Conference
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• 2001.10a
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• pp.21-24
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• 2001

Polyurethane are used for a wide range of commercial applications such as adhesives or coatings for various substrates including textile fabric, plastic, wood, glass fiber, and metals. The types of polyurethane ionomers have been reported according to the ionic charges on the polymer main chain, i.e. anionomer, cationomer, and zwitterconomers. (omitted)

• 한국신재생에너지학회:학술대회논문집
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• 2010.11a
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• pp.75.2-75.2
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• 2010

Polymer electrolyte fuel cells (PEFCs) have received a lot of attention as a power source for both stationary and mobile applications due to their attractive feature. In general, the performance of PEFCs is highly affected by the property of the electrodes. A PEFC electrode essentially consists of a gas diffusion layer and a catalyst layer. The gas difusion layer is highly porous and hydrophobicized with PTFE polymer. The catalyst layer usually contains electrocatalyst, proton conducting polymer, even PTFE as additive. Particularly, the proton conducting ionomer helps to increase the catalytic activity at three-phase boundary and catalyst utilization. Futhermore, it helps to retain moisture, resulting in preventing the electrodes from membrane dehydration. The most widely used proton conducting ionomer is perfluorinated sulfonic acid polymer, namely, Nafion from DuPont due to its high proton conductivity and good mechanical property. However, there are great demands for alternative ionomers based on non-fluorinated materials in terms of high temperature availability, environmental adaptability and production cost. In this study, the electrodes with the various content of the sulfonated poly(ether sulfone) ionomer in the catalyst layer were prepared. In addition, we evaluated electrochemical properties of the prepared electrodes containing the various amount of the ionomers by using the cyclic voltammetry and impedance spectroscopy to find an optimal ionomer composition in the catalyst layer.

• Restorative Dentistry and Endodontics
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• v.17 no.2
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• pp.355-364
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• 1992

This is a study on the effect of the dentinal pretreatment method to the bond strength between dentin and glass ionomer cement. In this study, 196 human molar teeth with sound crown were used. The dentin surfaces of these teeth were exposed with wet trimmer and polished with # 800 Emory paper and teeth were divided into 7 groups according to the pretreatment agent and method. Each group has 4 subroups of the kinds of glass ionomers. The shear bond strength were measured by Instron Universal Testing machine model 1122. The data of the evaluations were then subjected to statistical analysis using one way ANOVA and the result were as follows : 1. In Durelon liquid 20 sec scrubbing & Vitrebond filling subgroup, shear bond strength was highest with measurements of 72.41(kg/$cm^2$) and in no pretreatment & Shofu lining cement filling subgroup, lowest with measurements of 4.77(kg/$cm^2$). 2. In no pretreatment group, statistical significant differences were found between the subgroups of G-C lining cement and Shofu lining cement. 3. In Ketac conditioner 20 sec scrubbing group, Vitrebond were bonded stronger than others, and in Ketac conditioner 10 sec passive contact group, it has the significant difference with other glass ionomers except G-C lining cement. 4. The subgroup og G-C dentin conditioner 20 sec scrubbing & G-C lining cement filling was bonded to dentin stronger than the subgroup of no pretreatment & Shofu lining cement. In G-C dentin conditioner groups, both of 10 sec passive contact and 20 sec scrubbing, Vitrebond has highest bond strength among the subgroups. 5. The subgroup of Durelon liquid 10 sec passive contact & G-C lining cement filling was bonded to dentin stronger than the subgroup of no pretreatment & Shofu lining cement. Also in both Durelon liquid groups, Vitrebond were bonded to dentin with the highest strength among the subgroups.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.16 no.5
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• pp.3653-3659
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• 2015

This paper describes the reactive compatibilization of blends of a wholly aromatic thermotropic copolyester liquid crystalline polymer (TLCP) with random copolymers of ethylene and acrylic acid (EAA) and their salts. Blends were prepared by melt mixing in an intensive batch mixer, and the formation of a graft copolymer due to acidolysis between the TLCP and the acrylic acid group of the ionomer was evaluated. Chemical reaction was assessed by torque measurement during melt mixing and by thermal analysis and morphological observation. The Na-salt of the EAA ionomers was especially effective at promoting a grafting reaction. The extent of reaction depended not only on the cation, but also composition of the ionomer and reaction time. The product of the grafting reaction between the TLCP and a sodium-neutralized ionomer proved to be an effective compatibilizer for TLCP and EAA ionomers.

• Proceedings of the Membrane Society of Korea Conference
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• 1997.10a
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• pp.85-86
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• 1997

1. 서론 : Nanofiltration(NF)은 분자량이 200-1000인 유기물과 음이온 및 다가 이온등을 일가 이온으로부터 선택적으로 분리함으로써 유기물의 농축과 이온의 선택적인 분리를 동시에 행할 수 있는 분리 공정이며, 순수의 제조, 과일과 야채주스의 농축, 저알콜 맥주와 와인의 제조, 낙농 산업에서 유제품의 농축, 섬유공업에서 염료와 이온의 분리 및 제지공업의 폐수 처리 등에 응용되고 있다. NF용 막재료로는 셀룰로오스 계열의 고분자나 폴리아미드, 폴리술폰, PAN등이 연구되어 왔으며 최근에는 친수성이 좋고 가교를 하지 않고도 이온 결합에 의하여 강도를 유지할 수 있다는 아이오노머의 성질을 이용하여 아이오너마를 Nanofiltration용 막재료로 이용하려는 연구가 이루어지고 있다.[1-3] 그러나 아이오노머의 미세구조와 유기물의 분리특성간의 관계에 관한 연구는 미흡한 실정이다. 따라서 본 연구에서는 분리막의 성형성을 향상시키고자 알킬메타크릴레이트가 도입된 아이오너머를 합성하고 알킬기의 길이나 이온의 함량 등 고분자의 구조에 따른 아이오노머막의 분리특성을 연구하여 아이오노머막의 NF용막으로서의 응용가능성을 살펴보았다.

• Journal of the Korean Electrochemical Society
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• v.12 no.3
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• pp.219-233
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• 2009

Mobile devices in the next generation such as camera, cell phone, network, Note PC, etc. require higher power and energy sources due to convergences of various functions. Direct methanol fuel cell (DMFC) has been focused as an attractive power source, but there are critical issues involved in its commercialization with regard to the core technologies of materials, components, and system. The requirements of key technologies are differentiated from applications and fuel supply methods. Here, the roles of the proton-conducting membrane are discussed and the current status of DMFC systems is discussed in terms of proton conductivity, methanol permeability, and water management. Materials such as perfluorinated and partially fluorinated membranes, hydrocarbon membranes, composite membranes, and other modified ionomers have been studied. These would explain the critical issues of DMFC and the role of membranes for commercialization.

• Macromolecular Research
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• v.11 no.3
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• pp.198-201
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• 2003

Aqueous emulsion of polyurethane (PU) ionomers were reinforced with hydrophobic nanosilica to give composites. The aqueous emulsion was stable and the particle size increased as the content of hydrophobic nanosilica was increased. The reinforcing effect of nanosilica in mechanical properties of these composites were examined by dynamic mechanical and tensile tests, and the Shore A hardness was measured. Enhanced thermal and water resistance and marginal reduction in transparency of these composites were observed compared with pristine polymer. These results were similar with those of our previous studies on waterborne PU/organoclay nanocomposites.

• Proceedings of the Korean Vacuum Society Conference
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• 2001.07a
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• pp.143-144
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• 2001

• Membrane Journal
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• v.30 no.1
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• pp.57-65
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• 2020

The purpose of this study was to compare the water channel morphology and the proton conductivity by changing the number of repeating units of the polymer backbone of PEMs, and to present a criterion for selecting an appropriate polymer model for MD simulation. In the model with the shortest polymer main chain, the movement of the main chain and the sulfonic acid group was observed to be large, but no change in the water channel morphology was found. In addition, due to the nature of the proton transport ability that is most affected by the water channel morphology, the proton conductivity did not show a significant correlation with the length of the polymer backbone. These results provide important information, particularly for the preparation of ionomers for binders. In general, a low molecular weight polymer electrolyte material is used for a binder ionomer. Since the movement of the main chain/sulfonic acid group is improved, it can play a role of enclosing the catalyst layer well. However, there is no change in its proton conducting performance. In conclusion, the preparation of ionomers for binders will require molecular weight and structure design with a focus on physical properties rather than proton transfer performance.