• Bulletin of the Korean Chemical Society
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• v.16 no.11
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• pp.1133-1134
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• 1995

• Polymer(Korea)
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• v.26 no.2
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• pp.227-236
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• 2002

The structure of pregel state in thermoreversible poly(vinylidene fluoride)(PVDF) /propylene carbonate(PC) system was investigated by laser light scattering. It was found that the PVDF chain did not exist as a separate chain even in a very dilute concentration(i.e. 100 times more dilute than the gel formation concentration) but as a large spherical aggregate with the radius of gyration $R_G$, of 232 nm and the effective hydrodynamic radius $R_H$= of 407 nm at $40^{\circ}C$. Based upon experimental results such as $R_H/R_G$=ratio of 1.75 and the pattern of scattering intensity with a minimum, a core-shell type sphere model was suggested as a structure of the aggregate. According to this model, the radius of core part was estimated as 215 nm, the shell thickness as 192 nm, and the ratio of monomer density of the shell part to that of the core part as about 0.075.

• Proceedings of the Korean Fiber Society Conference
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• 2007.11a
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• pp.465-466
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• 2007

• Proceedings of the Membrane Society of Korea Conference
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• 2008.05a
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• pp.105-109
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• 2008

• Bulletin of the Korean Chemical Society
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• v.28 no.8
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• pp.1425-1428
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• 2007

• Proceedings of the Membrane Society of Korea Conference
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• 2004.05b
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• pp.69-72
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• 2004

So far the most practical polymer electrolytes are gel systems, which contain a polymeric matrix, a lithium salt, and aprotic organic solvents. This has met with success but has had disadvantages that the addition of solvents promotes deterioration of the electrolyte's mechanical properties and increases its reactivity towards the lithium metal anode.[1](omitted)

• Proceedings of the Korean Fiber Society Conference
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• 2001.10a
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• pp.432-435
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• 2001

Polymer/clay nanocomposites have received much attention in recent years, because they often exhibit physical properties that are dramatically different from those observed in their micro- and rnacrocornposite counterparts. The presence of clay may affect the crystallization behavior of semicrystalline polymer. (omitted)

• Polymer(Korea)
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• v.25 no.3
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• pp.367-374
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• 2001

The electromagnetic interference (EMI) shielding effectiveness (SE) of poly(vinylidene fluoride) (PVDF) composites was investigated using carbon nanofiber fillers prepared by catalytic chemical vapor deposition of various carbon-containing gases over Ni and Ni-Cu catalysts. The electrical conductivity of carbon nanofiber which was regarded as the key property of filler for the application of EMI shielding ranged from 4.2 to 22.4 S/cm at a pressure of 10000 psi. The electrical conductivity of carbon nanofiber/PVDF composites ranged from 0.22 to 2.46 S/cm and the EMI SE of those was in the range of 2∼13 dB. The electrical conductivity of carbon nanofibers increased with the increase in heat treatment temperature and time, while the electrical conductivity of the composites increased rapidly at the initial heat treatment and then approached a certain value with the further increase of heat treatment. The SE of the composites showed a maximum at the medium heat treatment and was proportional to the electrical conductivity of the composites. It was concluded that the specific surface area of carbon nanofibers decreased with the continual heat treatment and the specific surface area of filler was an important factor for the SE of the composites.

• Polymer(Korea)
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• v.37 no.2
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• pp.177-183
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• 2013

Surface properties such as morphology, crystalline structure, and chemical composition of poly(vinylidene fluoride) (PVDF)/poly(methyl methacrylate) (PMMA) blend coatings prepared by dispersion coating on poly(ethylene terephthalate) (PET) film have been investigated. It was observed that the surface properties were greatly influenced by the coating temperature and blend composition according to SEM, ATR-FTIR and XPS analysis. The typical surface morphology of ${\alpha}$-crystalline structure of PVDF could be observed when the coating temperature was lower than $120^{\circ}C$ or the amount of PVDF was higher than 80 wt% in the blend. Otherwise, the crystalline structure was changed from ${\alpha}$-crystal to ${\gamma}$-crystal or amorphous state. Based on the XPS analysis, the surface segregation of PVDF chains in the blend coating was confirmed.

• Journal of Adhesion and Interface
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• v.2 no.1
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• pp.18-22
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• 2001

Surface morphology of [poly(vinylidene fluoride)/poly(methyl methacrylate)] (PVDF/PMMA) was investigated on the basis of atomic force microscopy and differential scanning calorimeter measurements. The surface of (PMMA/PVDF) and (H14-PMMA/PVDF) blend films was fully composed with PVDF crystals. Although the difference of surface free energy between PMMA and PVDF is increased with increasing carboxyl group content in PMMA, however, in the case of (H24-PMMA/PVDF) blend film surface, the existence of aggregated H-PMMA was observed. It was found that the degree of surface enrichment of the blend is more affected by the magnitude of intermolecular interaction than the surface free energy difference, Besides, the introduction of carboxyl group for miscible (PVDF/PMMA) blend decreased the miscibility in the blend.