Single-walled carbon nanotubes (SWNTs)를 320 ℃에서 90분 동안 가열하여 비정질 탄소를 제거하고 남아 있는 금속 촉매를 제거하기 위해 염산에 24시간 처리하였다. 정제된 SWNT 표면에 산화반응을 통해 카복실기를 도입하였으며, 가혹한 환경으로 인해 길이가 짧아진 SWNT를 얻었다. 세정된 실리콘 웨이퍼를 3-aminopropyldiisopropylethoxysilane (3-APDIPES)의 톨루엔 용액에 담가 표면에 3-APDIPES의 자기 조립 단층막을 형성시켰다. SWNT의 카복실기와 3-APDIPES의 아미노기 사이의 산-염기 반응을 통해 생성되는 이온 사이의 정전기적 인력을 이용하여 실리콘 웨이퍼 표면에 SWNT를 배열하였다. Atomic Force Microscopy (AFM) 분석을 통해 반응시간과 농도에 따른 효과를 확인하였고, Transmission Electron Microscopy (TEM)을 이용해 산 처리 시간에 따른 효과를 확인하였다.

Multi-walled carbon nanotube (MWNT)를 황산과 질산의 혼산(3:1)에 넣고 상온에서 ultrasonication 을 가해주어 MWNT의 표면에 산화반응을 통하여 카복실기를 도입하였다. 세정된 실리콘 웨이퍼를 3-aminopropylethoxysilane (3-APDIPES)의 톨루엔 용액에 담그어 실리콘 웨이퍼 표면에 3-APDIPES의 자기 조립 단층막을 형성하였다. 이 과정에서 실리콘 웨이퍼 표면에 형성된 3-APDIPES 자기 조립 단층막의 두께는 8 Å 이며, 이 단층막이 매우 견고하게 실리콘 웨이퍼 표면에 결합되어져 있음을 확인하였다. MWNT의 카복실기와 3-APDIPES의 아미노기 사이의 산-염기 반응을 통하여 생성되는 이온 사이의 정전기적 인력을 이용하여 실리콘 웨이퍼 표면에 MWNT를 배열하였다. 이 때 얻어지는 MWNT의 배향은 수직 배향이 아니라 수평 배향임을 atomic force microscopy (AFM)와 field emission-scanning electron microscopy (FE-SEM) 분석을 통하여 확인하였다.

Amorphous carbon nanotubes were synthesized by a reaction of benzene, ferrocene and Na mixture in a small autoclave at temperatures as low as . The resulting carbon nanotubes were short and straight, but their inner hole was filled with residual products. The addition of quartz to the reacting mixture considerably promoted the formation of carbon nanotubes. A careful examination of powder structure suggested that the nanotubes in this process were mainly formed by surface diffusion of carbon atoms at the surface of solid catalytic particles, not by VLS(vapor-liquid-solid) mechanism.

In-situ processing route was adopted to disperse carbon nanotubes (CNTs) into powders homogeneously. The composite powders with homogeneous dispersion of CNTs could be synthesized by a catalytic route for in-situ formation of CNTs on nano-sized Fe dispersed powders. CNTs/Fe/ nanopowders were densified by spark plasma sintering (SPS). The hardness and bending strength as well as electrical conductivity increased with increasing sintering temperature. However, the electrical conductivity of the composites sintered at above showed decreased value with increasing sintering temperature due to the oxidation of CNTs

Aligned multi-wall carbon nanotubes (MWNTs) were synthesized through the catalytic decomposition of hydrocarbons in a quartz tube reactor. In this study, we investigated the influence of gas flow rate of feedstock on the structure and growth rate of vertically aligned carbon nanotubes produced by the floating catalyst method. As the flow rate of feedstock increased, the nanotube diameter became smaller and the length became longer. Although the growth rate also increased with the raise of flow rate, the optimum flow rate of feedstock existed for the crystallinity of carbon nanotubes.

Multi-walled carbon nanotubes (CNTs) were prepared by microwave plasma chemical vapor deposition (MPCVD) using various combination of binary catalysts and methane precursor. The maximum yield (10.3 %) of CNTs was obtained using a methane-hydrogen-nitrogen mixture with volume ratio of 1:1:2 at 1000 W of microwave power. As the microwave power increased up to 1000 W, the deposition yield of CNTs raised from 4.1 % to 10. 3 %. However, the prepared CNTs at 800 W showed the more crystalline structure than those prepared at 1000 W. The prepared CNTs over different binary catalysts had various structural conformations such as aligned cylinder, bamboo, and nanofibers. The Id/Ig value of CNTs overFe-Fe/Al2O3, Co-Co/Al2O3, and Co-Cu/Al2O3 were in the range of 0.89~0.93. Among the various binary catalysts used, Fe-Co./Al2O3 showed the highest yield.

Although the structure of carbon nanotubes is important factor characterizing its properties, it is very difficult to control the structure of carbon nanotubes (MWNTs) and to predict the range of their diameter, which is the primary factor of MWNTs' physical properties. We tried to control the diameter of MWNTsby governing the feed injection temperature of floating catalyst method. The structure of MWNTs was influenced by the phase change of ferrocene fed as the catalyst,. The carbon nanotubes were very narrow at injection temperatures close to the sublimation pt. of ferrocene, in which most MWNTs had diameters in the range of 20~30 nm. At injection temperatures between the boiling pt. and melting pt. of ferrocene, the diameters became larger and had broad distribution. However, at injection temperatures higher than the boiling pt., the diameters became narrow again and had very uniform distribution.

탄소재료는 결정구조에 따라 카본블랙(carbon black), 그라파이트(graphite), 탄소섬유(carbon fiber) 등 다양한 형태가 있으며 그 응용 또한 광범위하다. 이는 탄소재료가 화학적으로 매우 안정하고, 열 및 전기전도성이 우수하며, 기계적인 특성면에서도 고강도, 고탄성율을 가지고 있어서 구조적으로 안정하기 때문이다. 특히 (fullerene)와 탄소나노튜브(carbon naotube : CNT)등 근래 새로이 발견된 탄소물질들 은 그

Multi-walled carbon nanotubes (CNTs) were prepared by thermal chemical vapor deposition (CVD) and microwave plasma chemical vapor deposition (MPCVD) using various combination of binary catalysts with four transition metals such as Fe, Co, Cu, and Ni. In the preparation of CNTs from acetylene precursor by thermal CVD, the CNTs with very high yield of 43.6 % was produced over Fe-Co/Al2O3. The highest yield of CNTs was obtained with the catalyst reduced for 3 hr and the yield was decreased with increasing reduction time to 5 hr, due to the formation of FeAl2O4 metal-aluminate. On the other hand, the CNTs prepared by acethylene plasma CVD had more straight, smaller diameter, and larger aspect ratio(L/D) than those prepared by thermal CVD, although their yield had lower value of 27.7%. The degree of graphitization of CNTs measured by Id/Ig value and thermal degradation temperature were 1.04 and 602℃, respectively.