Carbon Nanotube Reinforced Composites: Metal and Ceramic ...
Carbon Nanotube Reinforced Composites: Metal and Ceramic ...
Carbon Nanotube Reinforced Composites: Metal and Ceramic ...
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
5<br />
<strong>Carbon</strong> <strong>Nanotube</strong>–<strong>Ceramic</strong> Nanocomposites<br />
5.1<br />
Overview<br />
The development of advanced technologies in the aeronautics, space <strong>and</strong> energy<br />
sectors requires high performance materials with excellent mechanical properties,<br />
high thermal conductivity <strong>and</strong> good wear resistance. <strong>Metal</strong>lic composites can meet<br />
these requirements but they suffer from corrosion <strong>and</strong> oxidation upon exposure to<br />
severe aggressive environments. Further, composite materials based on aluminum<br />
have a low melting point ( 643 C) that precludes their use as structural materials at<br />
elevated temperatures. <strong>Ceramic</strong>-based materials such as zirconia (ZrO2), alumina<br />
(Al2O3), silicon carbide (SiC), silicon nitride (Si3N4) <strong>and</strong> titanium carbide (TiC) have<br />
been used in industrial sectors at high temperatures due to their intrinsic thermal<br />
stability, good corrosion resistance, high temperature mechanical strength <strong>and</strong> low<br />
density. However, ceramics are known to exhibit low fracture toughness since plastic<br />
deformation in ceramics is very limited. Several approaches have been adopted to<br />
improve the fracture toughness of ceramics. These include transformation toughening,<br />
ductile-phase toughening <strong>and</strong> reinforcement toughening [1] (Figure 5.1).<br />
Transformation toughening involves the occurrence of phase transformation in<br />
zirconia-based ceramics to arrest the propagation of cracks. Pure zirconia exhibits<br />
three different crystalline structures: monoclinic (room temperature to 1170 C),<br />
tetragonal (1170–2370 C) <strong>and</strong> cubic (>2370 C). Several stabilizers or dopants are<br />
known to stabilize the tetragonal <strong>and</strong> cubic phases at room temperature in the<br />
metastable state [2, 3]. Partial stabilization enables retention of the metastable<br />
tetragonal phase of zirconia at ambient temperature by adding appropriate dopants<br />
such as MgO, CaO <strong>and</strong> Y2O3 (designated as M-TZP, C-TZP <strong>and</strong> Y-TZP). Under<br />
external stress loading, phase transformation from the tetragonal to the monoclinic<br />
phase occurs in the stress field around the crack tip [4]. This stress-induced tetragonal<br />
to monoclinic transformation is commonly referred to as martensitic transformation<br />
<strong>and</strong> somewhat similar to that in the carbon steels. Accompanying this<br />
transformation is a large increase in volume expansion. The resulting strain tends to<br />
relieve the stress field across the crack tip, thereby facilitating absorption of large<br />
fracture energy.<br />
j131