• Journal of Electrochemical Science and Technology
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• v.6 no.3
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• pp.81-87
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• 2015

This study introduces a facile strategy to prepare metal oxide/conducting polymer nanocomposites that may have promising applications in energy storage devices. Ploy aniline/nano wire manganese dioxide (PANI/NwMnO₂) was synthesized by cyclic voltammetry on glassy carbon electrode. Morphology and structure of the composite, pure PANI, MnO₂ nanowires were fully characterized using XRD and SEM analysis. Electrochemical studies shows excellent synergistic effect between PANI and MnO₂ nanowires which results in its capacitance increase and cycle stability against PANI electrode. Specific capacitances of PANI/NwMnO₂ and PANI were 456 and 190 F/g respectively. The electrochemical performance of electrodes studied using cyclic voltammetry, Galvanostatic charge/discharge and impedance spectroscopy.

• Journal of the Korean Ceramic Society
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• v.42 no.4
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• pp.224-231
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• 2005

The polymerization of $\varepsilon-caprolactone$ in the layers of the [DEACOOH]-Montmorillonite intercalations complex was attempted using 10-Carboxy-n-decyldimethylethylammonium bromide and Na-Montmorillonite to achieve [DEACOOH]-Polycaprolactone-Montmorillonite in which the inorganic material (montmorillonite) and the organic material (polycaprolactone) are chemically linked each other. The results of X-ray- and IR-analysis for the samples obtained after polymerization showed that the polymerization reaction has been successfully accomplished. In order to study the polymeric reaction products more precisely we have separated the polymerized product from the silicate layers and analyzed it with X-ray diffractometer, IR-spectrometer and TEM. The comparison of the results of X-ray- and IR-analysis for the separated polymer with them for the polymer which was synthesized by the reaction of $\varepsilon-caprolactone$ only with the organic cation without montmorillonite showed that the obtained both polymers are the same compounds.

• Proceedings of the Polymer Society of Korea Conference
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• 2006.10a
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• pp.357-357
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• 2006

Many industrial sources of proteins can be used as raw materials to produce films, molded materials, and various hollow items either by "casting" techniques or by "thermoplastic processing". Combining proteins with natural fibbers, paper or biodegradable polyesters is very promising to form biodegradable composites witch take advantage of the barrier and mechanical properties of each component. Using nano-fillers to form nanocomposites has also been shown to be interesting to improve properties. Production, with low transformation cost, of protein based materials to form biodegradable materials with controlled functional properties for food uses, medical uses, packaging, agriculture, controlled release systems, etc. is discussed.

• Steel and Composite Structures
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• v.37 no.1
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• pp.27-35
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• 2020

This study examines the wave propagation of the functionally graded polymer composite (FG-PC) nanoplates reinforced with graphene nanoplatelets (GNPs) resting on elastic foundations in the framework of the nonlocal strain gradient theory incorporating both stiffness hardening and softening mechanisms of nanostructures. To this end, the material properties are based on the Halpin-Tsai model, and the expressions for the classical and higher-order stresses and strains are consistently derived employing the second-order shear deformation theory. The equations of motion are then consistently derived using Hamilton's principle of variation. These governing equations are solved with the help of Trial function method. Extensive numerical discussions are conducted for wave propagation of the nanoplates and the influences of different parameters, such as the nonlocal parameter, strain gradient parameter, weight fraction of GNPs, uniform and non-uniform distributions of GNPs, elastic foundation parameters as well as wave number.

• Bulletin of the Korean Chemical Society
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• v.30 no.3
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• pp.671-674
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• 2009

In this work, high-aspect-ratio graphite nanofibers (GNFs) were used to improve the electrical, thermal, and mechanical properties of the poly(methyl methacrylate) (PMMA) polymer, as well as those of PMMA composites suitable for use in bipolar plates. In the result, an electrical percolation threshold for the composites was formed between 1 and 2 wt% GNF content. This threshold was found to be influenced strongly by the three separate stages of the meltblending process. The composites exhibited higher thermal and mechanical properties and lower thermal shrinkage compared with the neat PMMA. Thus, GNFs were demonstrated to have positive impacts on the thermo-mechanical properties of PMMA composites and showed, thereby, reasonable potential for use in composites employed in the fabrication of bipolar plates.

• Macromolecular Research
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• v.14 no.3
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• pp.312-317
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• 2006

In the preparation of a polyacrylonitrile (PAN)/sodium montmorillonite (Na-MMT) nanocomposite via an in-situ polymerization method, macroazoinitiator (MAI) was intercalated in the gallery of Na-MMT to enhance the delamination of silicate layers by intergallery polymerization. The exfoliated fine dispersion observed by X-ray diffraction pattern and transmission electron microscopy, the enhanced tensile storage modulus and the thermal decomposition temperature showed that the intercalated MAI was effective in inducing intergallery polymerization and that a poly(ethylene glycol) block linked to a PAN block improved the dispersion of hydrophilic Na-MMT in the polymer matrix.

• Macromolecular Research
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• v.17 no.11
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• pp.879-885
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• 2009

A macroazoinitiator (MAI) containing a poly(ethylene glycol) (PEG) segment was intercalated in the gallery of sodium montmorillonite (Na-MMT). Acrylic monomers were polymerized using this MAI intercalated in Na-MMT to prepare the acrylic copolymer nanocomposite (AN), which is a multiblock copolymer composed of two segments, an acrylic copolymer and PEG intercalated in Na-MMT (Na-MMT/PEG). When AN was used to modify the reactive hot melt polyurethane adhesive (RHA), the acrylic copolymer segment and Na-MMT/PEG synergistically enhanced the initial bond strength evolution and reduced the set time, even when the amount of Na-MMT in RHA was < 1 wt%. The viscosity of RHA increased and the tensile properties of the cured RHA film decreased due to modification with AN. These variations were more evident as the Na-MMT content in AN was increased.

• Advances in concrete construction
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• v.15 no.2
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• pp.75-84
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• 2023

Currently, polymer matrix nanocomposites (PMCs) are a prominent area of research due to their outstanding mechanical, thermal, and durability properties. The increase in recent studies justifies the possibility of using PMCs in structural retrofitting and reconstruction of damaged infrastructure and serving as new structural material. Using nanotechnology, nanocomposite panels in flooring combine concrete and steel, providing a very high level of performance. In sports flooring, high-performance concrete has become a challenge for reducing sports injuries and refinement in rehabilitation. As a composite material, this type of resistant concrete is one of the most durable and complex multi-phase materials. This article uses polyvinyl alcohol polymer (PVC) and multi-walled carbon nanotubes as concrete matrix fillers. Solution methods have been used for dispersing PVC and carbon nanotubes in concrete. The water-cement ratio, carbon nanotube weight ratio, and heat treatment parameters influenced the concrete nanocomposite's tensile and compressive strength. The dispersion of carbon nanotubes in cement paste and the observation of nano-microcracks in concrete was evaluated by scanning electron microscope (SEM).

• Polymer(Korea)
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• v.27 no.4
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• pp.377-384
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• 2003

High impact polystyrene/organically modified layered silicate (HIPS/OLS) nanocomposites by in situ polymerization were synthesized to investigate the effect of clay on the particle size and properties of rubber. In the OLS, the montmorillonite having benzyl group showed best dispersion in polystyrene phase. With the addition of clay, the intercalated peak from XRB was confirmed, but the peak gradually shifted to lower angle as rubber concentration increased. Thus, it is speculated that the organoclay disperses better in rubber phase than in polystyrene phase. The average rubber particle size increased and the particle size distribution widened as the amount of clay increased, which may be caused by the increase of the viscosity ratio of rubber to polystyrene phases and the unstable dispersion. The materials having clay showed improved thermal properties from thermogravimetric analysis. Rheological properties such as complex viscosity and storage modulus increased as the amount of clay increased.

• Polymer(Korea)
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• v.25 no.5
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• pp.691-698
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• 2001

Nanocomposites based on epoxy acid nanoclay were prepared employing organically modified mica type silicate (OMTS), diglycidyl ether of bisphenol A (DGEBA) type epoxy. curing agent (dicyandiamide; DICY), and catalyst (benzyl dimethyl amine; BDMA). Both melt mixing and solution mixing were und for the sample preparation and structural developments with curing reaction were analyzed using X-ray diffractometer (XRD) and small angle X-ray scattering (SAXS). Because of the different curing rate between extra-gallery and intra-gallery reactions of epoxy mixtures, only intercalated structure was observed for the sample prepared by melt mixing while fully exfoliated structure was observed for the sample prepared by solution mixing. Mechanical properties of exfoliated epoxy nanocomposite were investigated using a dynamic mechanical analyzer (DMA). The dynamic storage modulus of the nanocomposite in both glass and rubbery plateau regions were increased with increasing OMTS contents, but glass transition temperatures ($T_g$) remained unchanged. Thermal properties of epoxy nanocomposite were investigated using thermogravimetric (TGA) and limit oxygen index (LOI) methods. Thermal decomposition onset points and LOI values were increased with increasing OMTS contents due to barrier effects of OMTS sheets.