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Carbon Nanotube Reinforced Composites: Metal and Ceramic ...

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76j 2 <strong>Carbon</strong> <strong>Nanotube</strong>–<strong>Metal</strong> Nanocomposites<br />

Ni/MWNT coatings in a Watt-type bath producing more homogeneous or smooth<br />

surface coatings [106].<br />

It is widely recognized that Ni <strong>and</strong> Ni-P metallic coatings can also be deposited<br />

onto a substrate by means of electrodeless plating. Electrodeless Ni-P coatings have<br />

been used in many industrial applications due to their good corrosion <strong>and</strong> wear<br />

resistance as well as uniformity of thickness. Electrodeless plating can produce<br />

very smooth metallic coating from a solution via several chemical reactions without<br />

using electric power. Other advantages include ease of operation <strong>and</strong> good coverage<br />

in blind holes. Therefore, this technique is also very effective to deposit dense <strong>and</strong><br />

uniformly distributed nanotubes in the matrices of CNT–metal nanocomposites<br />

[107–109].<br />

2.8.2<br />

Co-Based Nanocomposites<br />

Hong <strong>and</strong> coworkers prepared in situ Co/MWNT nanocomposites by using a<br />

molecular level mixing method [110]. In the process, functionalized MWNTs were<br />

dispersed in oleylamine ultrasonically followed by adding the Co(II) acetylacetonate<br />

(Co(acac)2). The copper salt decomposed in oleylamine during refluxing in argon<br />

atmosphere into cube-shaped CoO nanoparticles of 50 nm. For comparison, pristine<br />

CoO nanopowders were also fabricated under similar conditions (Figure 2.29(a)<br />

<strong>and</strong> (b)). The X-ray diffraction pattern as shown in Figure 2.29(d)) confirms the<br />

formation of CoO nanocrystals in nanocomposite powder. The size of CoO nanocrystals<br />

is much smaller than that of CuO/MWNT composite powder (several<br />

micrometers) as described above. The CoO/MWNTpowder was reduced in hydrogen<br />

atmosphere to form the Co/MWNT composite powder. Such composite powder<br />

was consolidated by spark plasma sintering to produce bulk Co/7% MWNT nanocomposite.<br />

The grain size of consolidated Co/MWNTnanocomposite is 310 nm <strong>and</strong><br />

smaller than that of pure Co of 350 nm (Figure 2.30(a) <strong>and</strong> (b)). The SEM <strong>and</strong> highresolution<br />

TEM micrographs reveal homogeneous dispersion of MWNTs within the<br />

Co matrix (Figure 2.30(c) <strong>and</strong> (d)).<br />

As functionalization causes structural damage to nanotubes, Hong <strong>and</strong> coworkers<br />

used pristine MWNTs instead to prepare in situ Co/MWNT nanocomposites<br />

[111]. They dispersed pristine nanotubes in dioctyl ether (solvent) with<br />

oleylamine as a surfactant under mechanical stirring (Figure 2.31(a)). Subsequently,<br />

Co(acac) 2 <strong>and</strong> 1,2-hexadecanediol (reducing agent) were mixed with the nanotube<br />

suspension, followed by heating to the refluxing temperature of solvent. The<br />

nanotubes dispersed homogeneously in the solvent are effective nucleation sites<br />

for the heterogeneous nucleation of Co atoms (Figure 2.31(b)). The Co nuclei then<br />

grew <strong>and</strong> coalesced to form pearl-necklace-structured Co/MWNT powders in which<br />

Co nanoparticles are threaded by nanotubes (Figure 2.31(c)–(e)). No calcination or<br />

oxidation of matrix material is needed. Dense Co/MWNT nanocomposite can be<br />

prepared by directly sintering the synthesized powders. This procedure yields<br />

weaker interfacial nanotube-matrix bonding due to the absence of interfacial oxygen<br />

atoms. However, other functional properties, such as field emission, are enhanced

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