• 대한전기학회:학술대회논문집
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• 대한전기학회 2008년도 제39회 하계학술대회
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• pp.2307-2308
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• 2008

We observed internal space charge behavior for two types of epoxy composites under dc electric fields to investigate the influence of water at high temperature. In the case of glass/epoxy specimen, homocharge is observed at water-treated specimen, and spatial oscillations become clearer in the water-treated specimens. Electric field in the vicinity of the electrodes shows the injection of homocharge. In aramid/epoxy specimens, heterocharge is observed at water-treated specimens, i.e. negative charge accumulates near the anode, while positive charge accumulates near the cathode. Electric field is enhanced just before each electrode. In order to further examine the mechanism of space charge formation, we have developed a new system that allows in situ space charge observation during ion migration tests at high temperature and high humidity. Using this in situ system.

• Korean Chemical Engineering Research
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• 제49권3호
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• pp.301-305
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• 2011

ABS/실리케이트 복합체를 clay의 종류 및 함량을 변화시키며 에멀젼 중합을 이용하여 제조하였다. ABS의 화학구조는 적외선분광기(FT-IR)를 이용하여 이중결합 C-H 신축진동 피크(3000 $cm^{-1}$ 근처)의 변화를 통해 확인하였다. ABS/실리케이트 복합체의 열적특성은 시차주사열용량분석기(DSC) 와 열중량분석기(TGA)를 이용하여 관찰하였다. Clay의 종류에 따른 ABS의 유리전이온도에는 큰 변화가 나타나지 않음을 알 수 있었다. TGA에 의한 분해온도는 20A의 함량이 3 wt%인 ABS/20A 복합체에서 가장 높은 값을 나타내었다. 복합체의 실리케이트 분산정도는 X-선회절(XRD)법을 이용하여 측정하였다. ABS/20A 복합체의 실리케이트 분산은 20A 함량에 의존하였고, 함량이 5 wt% 이상 첨가되었을 때 20A의 회절 피크가 나타나는 것을 확인하였다.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1998년도 가을 학술발표회논문집
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• pp.236-239
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• 1998

The in situ composites based on poly(ethylene 2,6-naphthalate) and thermotropic liquid crystalline polymer (LCP) have been an area of increasing interest and study, since LCP exhibits high chemical stabilities and excellent thermo mechanical properties such as high strength and modulus. In a binary, however, poor compatibility and interfacial adhesions between two phases frequently results in deteriorated mechanical properties. (omitted)

• 한국분말재료학회지
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• 제9권6호
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• pp.394-408
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• 2002

Nanostructured high strength metastable Al-, Mg- and Ti-based alloys containing different amorphous, quasicrystalline and nanocrystalline phases are synthesized by non-equilibrium processing techniques. Such alloys can be prepared by quenching from the melt or by powder metallurgy techniques. This paper focuses on one hand on mechanically alloyed and ball milled powders containing different volume fractions of amorphous or nano-(quasi)crystalline phases, consolidated bulk specimens and, on the other hand. on cast specimens containing different constituent phases with different length-scale. As one example. $Mg_{55}Y_{15}Cu_{30}$- based metallic glass matrix composites are produced by mechanical alloying of elemental powder mixtures containing up to 30 vol.% $Y_2O_3$ particles. The comparison with the particle-free metallic glass reveals that the nanosized second phase oxide particles do not significantly affect the glass-forming ability upon mechanical alloying despite some limited particle dissolution. A supercooled liquid region with an extension of about 50 K can be maintained in the presence of the oxides. The distinct viscosity decrease in the supercooled liquid regime allows to consolidate the powders into bulk samples by uniaxial hot pressing. The $Y_2O_3$ additions increase the mechanical strength of the composites compared to the $Mg_{55}Y_{15}Cu_{30}$ metallic glass. The second example deals with Al-Mn-Ce and Al-Cu-Fe composites with quasicrystalline particles as reinforcements, which are prepared by quenching from the melt and by powder metallurgy. $Al_{98-x}Mn_xCe_2$ (x =5,6,7) melt-spun ribbons containing a major quasicrystalline phase coexisting with an Al-matrix on a nanometer scale are pulverized by ball milling. The powders are consolidated by hot extrusion. Grain growth during consolidation causes the formation of a micrometer-scale microstructure. Mechanical alloying of $Al_{63}Cu_{25}Fe_{12}$ leads to single-phase quasicrystalline powders. which are blended with different volume fractions of pure Al-powder and hot extruded forming $Al_{100-x}$$(Al_{0.63}Cu_{0.25}Fe_{0.12})_x$ (x = 40,50,60,80) micrometer-scale composites. Compression test data reveal a high yield strength of ${\sigma}_y{\geq}$700 MPa and a ductility of ${\varepsilon}_{pl}{\geq}$5% for than the Al-Mn-Ce bulk samples. The strength level of the Al-Cu-Fe alloys is ${\sigma}_y{\leq}$550 MPa significantly lower. By the addition of different amounts of aluminum, the mechanical properties can be tuned to a wide range. Finally, a bulk metallic glass-forming Ti-Cu-Ni-Sn alloy with in situ formed composite microstructure prepared by both centrifugal and injection casting presents more than 6% plastic strain under compressive stress at room temperature. The in situ formed composite contains dendritic hcp Ti solid solution precipitates and a few $Ti_3Sn,\;{\beta}$-(Cu, Sn) grains dispersed in a glassy matrix. The composite micro- structure can avoid the development of the highly localized shear bands typical for the room temperature defor-mation of monolithic glasses. Instead, widely developed shear bands with evident protuberance are observed. resulting in significant yielding and homogeneous plastic deformation over the entire sample.

• 한국재료학회지
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• 제8권10호
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• pp.938-944
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• 1998

$MoSi_2$에 W분말을 첨가하여 $MoSi_2$/W 복합재료를 $1600^{\circ}C$에서 3시간 동안 유지하면서 30MPa의 조건하에서 고온진공 가압기를 이용하여 제조하였으며, 텅스텐 분말의 첨가량이 $(Mo)Si_2$의 미세조직과 기계적 성질에 미치는 영향을 조사하였다. 텅스텐은 몰리브덴과 치환하면서 고용체 합금을 이루었으며, 입자의 크기는 텅스텐 분말의 첨가량이 증가할수록 감소하였다. 비커스경도는 텅스텐 분말의 첨가량이 증가할수록 향상되었으나, 반면에 압흔파단 강도는 오히려 감소되었다. 10%정도의 텅스텐 분말을 첨가하였을 때, 압흔파단 강도가 $4.5MPa$\sqrt{m}$로서 순수 $MoSi_2$의 $2.7MPa\sqrt{m}$에 비하여 향상되었음을 알 수 있었다.

• Smart Structures and Systems
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• 제5권6호
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• pp.633-644
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• 2009

A simple method has been developed to detect the bonding condition of active fiber composites (AFC) adhered to the surface of a host structure. Large deformation actuating capability is one of important features of AFC. Edge delamination in adhesive layer due to large interfacial shear stress at the free edge is typically resulted from axial strain mismatch between bonded materials. AFC patch possesses very good flexibility and toughness. When an AFC patch is partially delaminated from host structure, there remains sensing capability in the debonded part. The debonding size can be determined through axial resonance measured by the interdigitated electrodes symmetrically aligned on opposite surfaces of the patch. The electrical impedance and modal response of the AFC patch in part adhered to an aluminum plate were investigated in a broad frequency range. Debonding ratio of the AFC patch is in inverse proportion to the resonant frequency of the fundamental mode. Feasibility of in-situ detecting the progressive delamination between AFC patch and host plate is demonstrated.

• 대한기계학회논문집A
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• 제39권6호
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• pp.567-573
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• 2015

본 논문은 저온과 고온 환경 하에서 카본/에폭시 복합재의 기계적 물성 변화를 평가하는데 목적을 두고 있다. 기계적 물성 변화 평가는 환경 챔버와 전기로를 이용하여 $-40^{\circ}C$에서 $220^{\circ}C$까지의 온도에 대해 섬유방향과 섬유 직각방향의 인장 물성, 면내 전단 물성 그리고 층간전단강도에 대해 평가를 수행하였다. $-40^{\circ}C$ 저온환경에서의 기계적 물성은 상온에서의 물성보다 증가하는 것을 확인하였다. 섬유방향 물성은 온도가 증가함에 따라 물성저하가 서서히 발생하였으나, 섬유직각방향 물성, 면내전단 물성 그리고 층간전단강도는 $140^{\circ}C$ 이상의 온도에서 수지의 유리전이로 인해 급격한 물성저하가 발생하는 것을 확인하였다. $100^{\circ}C$ 환경에서 섬유 직각방향 인장물성 증가의 직접적인 원인은 수지의 후경화로 인한 현상으로 판단된다.

• Macromolecular Research
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• 제17권8호
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• pp.609-615
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• 2009

Two types of nano composite were obtained by in situ chemical method in polyaniline (PANI)/dodecyl-benzenesulfonic acid (DBSA) system depending on the use of either ammonium persulfate (APS) or ferric chloride ($FeCl_3$) as the oxidant. In order to study the difference of the two composites in the surface characteristics, thermal stability, and electric properties, the composite films were studied by transmission electron microscopy (TEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and temperature dependent DC electrical conductivity. The results revealed a large difference in the surface morphology, thermal stability, and the microstructure properties between the two composites, and these differences were considered responsible for the molecular order and conductivity.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2008년도 제39회 하계학술대회
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• pp.1228-1229
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• 2008

The composites were fabricated 61[vol.%] ${\beta}$-SiC and 39[vol.%] $TiB_2$ powders with the liquid forming additives of 12[wt%] $Al_2O_3+Y_2O_3$ as a sintering aid by pressure or pressureless annealing at 1,650[$^{\circ}C$] for 4 hours. Reactions between SiC and transition metal $TiB_2$ were not observed in the microstructure and the phase analysis of the SiC-$TiB_2$ electroconductive ceramic composites. Phase analysis of SiC-$TiB_2$ composites by XRD revealed mostly of ${\alpha}$-SiC(6H), $TiB_2$, and In Situ $YAG(Al_5Y_3O_{12})$. The relative density, the flexural strength and the Young's modulus showed the highest value of 88.32[%], 136.43[MPa] and 52.82[GPa] for pressure annealed SiC-$TiB_2$ composites at room temperature. The electrical resistivity showed the lowest value of 0.0162[${\Omega}{\cdot}cm$] for pressure annealed SiC-$TiB_2$ composite at 25[$^{\circ}C$]. The electrical resistivity of the pressure annealed SiC-$TiB_2$ composite was positive temperature coefficient resistance (PTCR) but the electrical resistivity of the pressureless annealed SiC-$TiB_2$ composites was negative temperature coefficient resistance(NTCR) in the temperature ranges from 25[$^{\circ}C$] to 700[$^{\circ}C$].

• 한국세라믹학회지
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• 제28권7호
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• pp.549-555
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• 1991

Mullite-zirconia (0∼4 mol% yttria) composites were obtained by In-situ sintering of zircon and alumina mixture, and their mechanical properties were studied in conjuction with microstructure observation. Martensitic transformation temperature (Ms) of zirconia dispersed in the mullite matrix decreased with Y2O3 contents and was about 600$^{\circ}C$ for ZrO2 containing 4 mol% Y2O3. On cooling of this composites, tetragonal to monoclinic phase transformation induced microcracks at the grain boundary of mullite matrix. The microcracks seemed to absorb the fracture energy in stress field during mechanical tests. Therefore, toughening mechanisms of this composite were considered to nucleation and extension of microcrack, and crack deflection mechanism due to the difference of thermal expansion coefficient between matrix and dispersed phase.