연료전지는 석유엔진과 비교하여 높은 전류밀도와 효율성, 그리고 친환경적이기 때문에 21세기 들어 대체 발전시스템으로서 각광받아왔다. 연료전지 시스템에서 고분자 전해질 막은 핵심부품으로써 현재 Nafion막이 연료전지시스템에서 사용 중이지만 높은 제조단가와 고온에서 낮은 전도도를 가지는 단점을 가지고 있다. 그러므로 많은 학자들이 낮은 제조단가, 높은 물리적 특성들을 달성하기 위한 연구를 진행하여 왔으며 연료전지의 상용화와 동시에 고성능의 연료전지의 개발을 위하여 많은 방법들이 개발되어 왔다. 그중, 유무기 복합막은 유기물과 무기물의 물성을 균일하게 조합할 수 있으므로 잠재성을 가지고 있는 제조방법이다. 본고에서는 다양한 무기물이 사용되어 제조된 유무기 복합막의 연구동향에 대하여 조사하였다.

A cobalt oxide - tin oxide nanocomposite based gas sensor on an SiO2 substrate was fabricated. Granular thin film of tin oxide was formed by a rheotaxial growth and thermal oxidation method using dc magnetron sputtering of Sn. Nano particles of cobalt oxide were spin-coated on the tin oxide. The cobalt oxide nanoparticles were synthesized by polymer-assisted deposition method, which is a simple cost-effective versatile synthesis method for various metal oxides. The thickness of the film can be controlled over a wide range of thicknesses. The composite structures thus formed were characterized in terms of morphology and gas sensing properties for reduction gas of H2. The composites showed a highest response of 240% at 250˚C upon exposure to 4% H2. This response is higher than those observed in pure SnO2 (90%) and Co3O4 (70%) thin films. The improved response with the composite structure may be related to the additional formation of electrically active defects at the interfaces. The composite sensor shows a very fast response and good reproducibility.

Liquefied-wood polymer composite was prepared and mechanical properties was evaluated to develop potential utility of liquefied wood. The liquefied wood was made from waste wood and chemical modified with acetic anhydride and maleic anhydride (MA), phtalic anhydride (PA). The composite sheet was prepared from modified liquefied-wood and polymer(PE). The mechanical, chemical and microscopical properties composite sheet were investigated. The results were summarized as follows, 1. The tensile strength was increased and breaking elongation of composite sheet was decreased with the time of acetylation and the dosage of MA. 2. The Young's modulus of composite sheet was gradually decreased with the dosage of PA. 3. The peak intensity of 1737cm-1 in FT-IR spectra of chemical modified liquefied woods was increased. 4. The dispersity of liquefied woods with PE was improved with chemical modification.

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 nanowireswere synthesized via an aqueous solution method at a low temperature, and the nanowire densities inside thecomposites were controlled by changing the ultrasonifiaction time. The channel layers were prepared withcomposites by spin-coating at 2000rpm, which was followed by annealing in a vacuum at 100oC for 10 hours.Au/inorganic-organic composite layer/SiO2 structures were fabricated and the mobility, Ion/Ioff ratio, andthreshold voltage were then measured to analyze the electrical characteristics of the channel layer. Comparedwith a P3HT TFT, the electrical properties of TFT were found to be improved after increasing the nanowiredensity inside the composites. The mobility of the P3HT TFT was approximately 10-4cm2/V·s. However, themobility of the ZnO nanowire/P3HT composite TFT was increased by two orders compared to that of theP3HT TFT. In terms of the Ion/Ioff ratio, the composite device showed a two-fold increase compared to thatof the P3HT TFT.

폴리스티렌-블록-폴리히드록에틸 메타크릴레이트(PS-b-PHEMA), 술포석시닉산(SA), 인텅스텐산(PWA)으로 구성된 수소 이온 전도성 나노복합 고분자 전해질막을 제조하였다. 폴리히드록에틸 메타크릴레이트(PHEMA) 블록의 히드록실그룹(-OH)와 술포석시닉산(SA)의 -COOH 그룹과의 에스테르 반응에 의하여 전해질막을 가교시켰다. 폴리헤테로산(PWA)을 도입했을 때, SO3 - 그룹의 신축 밴드가 1187 cm -1에서 1158 cm -1로 낮아졌으며, 이는 PWA 입자가 전해질막의 술폰산 그룹과 상호작용함을 나타낸다. PWA 함량이 30wt%가 되었을 때, 상온 전도도는 0.045에서 0.062S/cm로 증가되었으며, 이는 PWA 입자의 고유 전도도 특성과 전해질막의 술폰산기의 산도가 증가했기 때문이다. 또한 30wt%를 함유한 복합 전해질막은 100℃에서는 최대 0.126 S/cm의 수소 이온 전도도를 나타내었다 PWA가 첨가됨에 따라 복합 전해질막의 열적특성 또한 증가하였다.

Polyvinylalcohol (PVA)을 전해질 막으로 이용하여 위하여 가교제로서 sulfosuccinic acid (SSA)와 무기물 첨가제로 phosphotungstic acid (PWA), silicotungstic acid (SiWA) 등의 HPA (heteropolyacid)를 사용하여 PVA/SSA/HPA 복합막을 제조하였다. PVA/SSA/HPA 복합막은 HPA의 농도가 증가함에 따라 함수율은 감소하였으나 IEC값은 증가하는 경향을 나타내었다. PVA/SSA/HPA 복합막의 XRD 분석 결과 HPA의 농도가 증가함에 따라 HPA가 복합막 속으로 잘 분산되는 것을 확인할 수 있었으며 HPA로서 PWA보다 SiWA의 분산성이 우수하였다. TGA 분석결과 PVA/SSA 복합막은 가교 결합으로 인하여 PVA 보다 열안정성이 우수하였으며 복합막의 HPA의 농도가 증가할수록 열안정성이 더욱 증대되는 것을 알 수 있었다. PVA/SSA/HPA 복합막의 메탄올 투과저항은 Nafion보다 현저히 우수하였으며 HPA의 농도가 증가할수록 메탄올의 투과도는 감소하였다.

본 연구에서는 흑연, 열경화성 수지, 그리고 카본 블랙을 사용하여 조성과 제조 조건을 달리하여서 탄소 복합체를 제조하였다. 제조된 탄소 복합체의 고분자 전해질 연료전지용 bipolar plate로의 응용 가능성을 살펴보기 위하여 연속 흐름 기체 투과 장치를 사용하여서 산소의 투과도를 측정하였다 실험 결과 카본 블랙의 양이 증가할수록 산소 투과도가 증가하였으며, 탄소 복합체의 성형 시간이 증가할수록 투과도가 감소하였다 반면에 성형 압력은 산소 투과도에 큰 영향을 미치지 않음을 알 수 있었다.

Two-component ceramic (alumina-zirconia) composites were fabricated by a soft-solution process in which polyethylene glycol (PEG) was used as a polymeric carrier. Metal salts and PEG were dissolved in ethyl alcohol without any precipitation in 1:1 volume ratio of alumina and zirconia. In the non-aqueous system, the flammable solvent made explosive, exothermic reaction during drying process. The reaction resulted in formation of volume expanded, porous precursor powders by a vigorous decomposition of organic components in the precursor sol. The PEG content affected the grain size of sintered composites as well as the morphology of precursor powders. The difference of microstructure in sintered composite was attribute to the solubility and homogeneity of metal cations in precursor sol. At the optimum amount of the PEG polymer, the metal ions were dispersed effectively in solution and a homogeneous polymeric network was formed. It made less agglomerated particles in the precursor sol and affected on uniform grain size in sintered composite.

금속이온 분리를 위한 운반체 지지형 (고분자/운반체) 복합막을 수면전개법에 의하여 제조하였다. 이들 막의 형상은 전개용액의 물성에 의하여 영향을 받는다. (고분자/18-crown-6) 복합용액의 표면장력은 18-crown-6의 농도가 증가함에 따라 감소하는 경향을 나타내며, 고분자에 따른 용액의 표면장력은 PVC>PS>CA 순서로 감소하였다. 점도는 18-crown-6의 농도가 증가함에 따라 PVC계와 PS계 용액은 큰 변화가 없으나 CA계 용액은 감소하는 경향을 나타내었다. 18-crown-6 환형고리분자는 고분자쇄 사이에서 전기적인 완충역할을 하여 고분자쇄간의 분자간력을 약화시켜줌으로써 복합 용액의 전개성을 증가시켰다. 복합박막의 표면형상은 단일박막보다 균일하였으며, 18-crown-6가 증가함에 따라 전후면은 모두 균일한 구조극 나타내었다.

The phase separated structure and the electo-optical properties of the polymer /liquid crystal(LC) composite films including a dye were investigated. The phase separated structure of the polymer /LC / dye composite film(GH composite film) including below 2wt% dye against LC was almost same with the composite film which does not include dye. But the electro-optical properties of the GH composite film strongly depended on weight fraction of the dye against the LC. The response time of the GH composite film increased with the increase of the dissolved dye in LC because the dye acts as a registivity for the orientation of LC molecules by the electric filed.

The phase separated structure and the electro-optical properties of the (polymer/liquid) crystal : LC) composite film strongly depended on the weight fraction of LC in it. The continuous LC phase was formed in a three-dimensional polymer network when the LC weight fraction was above 40wt%. The aggregation structure of the composite film could be controlled by controlling the solvent evaporation velocity during the film preparation process. The smaller LC domains or channels were formed in the case of the faster solvent evaporation velocity. The composite film exhibited reversible light scattering-light transmission switching upon electric field -OFF and -ON states, respectiverly. The light scattering properties of the composite film strongly depended on the spatial distortion of the nematic directors as well as the mismatch in refractive indices between matrix polymer and LC.

Plastic기 복합재료의 파괴거동에 미치는 원공크기오 판폭의 영향을 검토하기 위하여 단축인장시험을 행하였다. 점응력파손조건에서의 특성길이 do는 원공크기 및 판폭에 의존하며, 이를 기초로 파손강도를 예측하기 위한 수정 점응력 파손조건식을 제안하였다. 이 파손조건의 예측값은 실험값과 잘 일치하였다. 파손 강도는 원공선단의 손상비의 증가에 따라 증가하며, 이는 손상영역의 형성으로 인한 응력완화현상으로 설명되어 진다. 또한 불안정 파괴시의 최대균열길이 ac는 특성길이 do의 약 2배의 값을 나타낸다. 파괴인성에 대응하는 한계에너지해방율 Gc의 변화는 원공선단의 손상영역의 증가에 의한 응력완화가 주요한 원인이라고 할 수 있다.

Background : The objective of this study was to make colloidal dispersion of the active compound was characterized nano-composite from radix of Angelica gigas Nakai using hot melt extrusion (HME). Therefore, food grade hydrophilic polymer matrices was used to disperse compound in aqueous media. Methods and Results : Extrudate solid formulations (ESFs) mediated various HPMCs (hydroxypropyl methylcellulose) and Na-Alg polymer from ultrafine powder of radix of Angelica gigas Nakai was developed through physical crosslink method (HME) with ionization agent (treatment of acetic acid) and food grade polymer [HPMCs such as HP55, CN40H, AN6 and sodium alignate (Na-Alg)]. X-ray powder diffraction (XRD) analysis confirmed the amorphization of crystal compounds in extrudate solid formulations mediated HP55 (HP55-ESF). Differential scanning calorimetry (DSC) analysis indicated a lower enthalpy (ΔH = 10.62 J/g) of glass transition temperature (Tg) in HP55-ESF. Infrared fourier transform spectroscopy (FT-IR) reveled new functional groups produced in HP55-ESF. Phenolic compound, flavonoid (including decursin and decursinol angelate) and antioxidant activity increased at 5, 10 and 2 times in HP55-ESF. Water solubility (61.5%) nano size (323 ㎚) particle was achieved in the HP55-ESF. Conclusion : Nano-composites have been developed utilizing melt-extruded solid dispersions technology by food grade polymer enhanced nano dispersion (< 500 ㎚) of active compound from radix of Angelica gigas Nakai with enhanced solubility and bioavailability. This nano-composites of radix of Angelica gigas Nakai developmental and marketed products to enable therapeutic performance.

This is A Study on the Bond Performance of Synthetic Polymer Composite Waterproofing and Anticorrosion Method in accordance with PE Fiber Reinforcement. Test results, A Bond Performance of the Test Specimen was confirmed to have increased 37.5%. By PE Fiber Reinforcement.