• Composites Research
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• v.32 no.6
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• pp.342-348
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• 2019

Development of flame retarding polymer based materials has been studied actively due to the increase in use of polymers. The post treatment of manufactured fibers or the introduction of flame retardant into fibers is representative method for the way to improve the flame retardancy. Among the polymers, polyacrylonitrile (PAN), which is a precursor of carbon fiber, has been widely used for clothes. Due to low flame retardancy of PAN fiber (LOI value: 17~18%), the improvement of flame retardancy of PAN fiber is needed. In this review paper, we report preparation methods for the fabrication of post-treated (oxidization or chemical reaction) flame-retarding PAN fibers and composites composed of PAN and organic/inorganic materials (SiO₂, 2D materials or CNT).

• Korean Journal of Materials Research
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• v.19 no.1
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• pp.33-36
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• 2009

Inorganic-organic composite thin-film-transistors (TFTs) of ZnO nanowire/Poly(3-hexylthiophene) (P3HT) were investigated by changing the nanowire densities inside the composites. Crystalline ZnO nanowires were synthesized via an aqueous solution method at a low temperature, and the nanowire densities inside the composites were controlled by changing the ultrasonifiaction time. The channel layers were prepared with composites by spin-coating at 2000 rpm, which was followed by annealing in a vacuum at $100^{\circ}C$ for 10 hours. Au/inorganic-organic composite layer/$SiO_2$ structures were fabricated and the mobility, $I_{on}/I_{off}$ ratio, and threshold voltage were then measured to analyze the electrical characteristics of the channel layer. Compared with a P3HT TFT, the electrical properties of TFT were found to be improved after increasing the nanowire density inside the composites. The mobility of the P3HT TFT was approximately $10^{-4}cm^2/V{\cdot}s$. However, the mobility of the ZnO nanowire/P3HT composite TFT was increased by two orders compared to that of the P3HT TFT. In terms of the $I_{on}/I_{off}$ ratio, the composite device showed a two-fold increase compared to that of the P3HT TFT.

• Korean Chemical Engineering Research
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• v.55 no.4
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• pp.483-489
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• 2017

The loss of the sulfur cathode material through dissolution of the polysulfide into electrolyte causes a significant capacity reduction of the lithium-sulfur cell during the charge-discharge reaction, thereby debilitating the electrochemical performance of the cell. We addressed this problem by using a chemical and physical approach called reduction of polysulfide dissolution through direct coating functional inorganic (graphene oxide) or organic layer (polyethylene oxide) on electrode, since the deposition of external functional layer can chemically interact with polysulfide and physically prevent the leakage of lithium polysulfide out of the electrode. Through this approach, we obtained a composite electrode for a lithium-sulfur battery (sulfur: 60%) coated with uniform and thin external functional layers where the thin external layer was coated on the electrode by solution coating and drying by a subsequent heat treatment at low temperature (${\sim}80^{\circ}C$). The external functional layer, such as inorganic or organic layer, not only alleviates the dissolution of the polysulfide electrolyte during the charging/discharging through physical layer formation, but also makes a chemical interaction between the polysulfide and the functional layer. As-formed lithium-sulfur battery exhibits stable cycling electrochemical performance during charging and discharging at a reversible capacity of 700~1187 mAh/g at 0.1 C (1 C = 1675 mA/g) for 30 cycles or more.

• Proceedings of the Korean Ceranic Society Conference
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• 2003.04a
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• pp.207.1-207
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• 2003

• 한국전기화학회:학술대회논문집
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• 2002.04a
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• pp.42-42
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• 2002

• Proceedings of the Materials Research Society of Korea Conference
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• 2005.05a
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• pp.317-317
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• 2005

• Proceedings of the Korean Nuclear Society Conference
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• 1998.10a
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• pp.296-296
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• 1998

• Journal of Biomedical Engineering Research
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• v.10 no.2
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• pp.89-90
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• 1989

To develop an artificial bone substitute that is gradually degraded and replaced by the regenerated natural bone, the authors designed and produced a composite that is consisted of calcium phosphate and collagen. Human umbilical cord origin pepsin treated type I atelocollagen was used as the structural matrix, by which sintered or non-sintered carbonate apatite was encapsulated to form an inorganic-organic composite. With cross linking atelocollagen by UV ray irradiation, the resistance to both compressive and tensile strength was increased. Collagen degradation by the collagenase induced collagenolysis was also decreased.

• Proceedings of the Membrane Society of Korea Conference
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• 2003.07a
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• pp.37-40
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• 2003

Mesoporous zeolite - heteropolyacid-polymer hybrid membrane was prepared by sol-gel processes to make a proton conducting membrane. The crystallinity of mesoporous zeolite in composite membrane was increased with contents of heteropolyacid. Proton conductivity obtained from impedance measurements increases with contents of heteropolyacid, about 10$^{-3}$ S/cm in ca. 1.5 Wt% heteropolyacid.

• Proceedings of the Membrane Society of Korea Conference
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• 2004.05a
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• pp.144-147
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• 2004

Organosilicon polymers have long paid attention as functional polymers [1,2]. Among others, poly- (1-trimethylsilyl-1-propyne) [PTMSP] is a polymer, which forms a gas separating membrane with extraordinary high gas permeability. In particular, composite membranes that constituted two different matrices (inorganic and organic) have been recently developed in order to improve the permeation characteristics.(omitted)