Microstructure and Mechanical Properties of High-Strength Graphite Particles Coated TiO2 Film Embedded in SiC Composite

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Abstract:

In order to improve the fracture strength of Gp/SiC composites, the mean size (d50) 50 μm high-strength graphite particles, TiCl4 used as starting materials, and the graphite particles coated TiO2 film were obtained using co-precipitation method. Then the Gp/SiC composites were prepared with the “roll the snowball method” and hot-pressing sintering technology. The microstructure and phase constitution is measured by scanning electron microscopy (SEM) and electron energy spectrum (EDS). It is found that the coated graphite cores are embedded in the SiC matrix as the islands. The apparent porosity increases, density decreases, with graphite content increasing. The fracture strength and hardness decrease, fracture toughness increases with the graphite content increasing. The apparent porosity, density, fracture strength, fracture toughness, hardness of the composite are 3.8%, 2.61 g•cm-3,135 MPa, 2.82 MPa•m1/2,22.1 GPa, respectively, while the volume percent of ceramic and graphite is 6︰4 and sintered at 2000°C. The TiO2 film can effectively lower the sintering temperature and impart composite better mechanical properties. The toughening mechanisms are crack deflection and branching as well as stress relaxation near the crack tip.

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Advanced Materials Research (Volumes 194-196)

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1768-1771

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February 2011

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© 2011 Trans Tech Publications Ltd. All Rights Reserved

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[1] P. Filip, Z. Weiss and D. Rafaja: Wear. Vol. 252 (2002), pp.189-198.

Google Scholar

[2] S. Varadarajan, A.K. Pattanaik and V.K. Sarin: Surf. Coat Technol. Vol. 139 (2001), pp.153-160.

Google Scholar

[3] H. Fritze, J. Jojie, T. Witke, et al:J. Eur. Ceram. Soc. Vol. 18 (1998), pp.2351-2364.

Google Scholar

[4] F. Smeacetto and M. Ferraris: Carbon. Vol. 40 (2002), pp.583-587.

Google Scholar

[5] S. Lloyd, N. Avery and M. Pal: Carbon. Vol. 39 (2001), pp.991-999.

Google Scholar

[6] P. Olivier and D. Alain. Chem. Vap. Deposit. Vol. 61 (2000), pp.41-50.

Google Scholar

[7] L. Yu, J. ZHAO, X.Y. Yue, et al: Advanced Materials Research. Vols. 105-106 (2010) pp.855-858.

Google Scholar

[8] X.Y. Yue, S. M. Zhao, P. Lü, et al: Materials Science and Engineering A. Vols. 527 (2010) , pp.7215-7219.

Google Scholar

[9] M.W. Chen, J.W. McCauley, J.C. LaSalvia, et al., J. Am. Ceram. Soc. Vols. 88 (2005) p.1935-(1942).

Google Scholar

[10] K.V. Emtsev, Th. Seyller, L. Ley, et al: Phys. Rev. B Vol. 73 (2006), p.075412.

Google Scholar

[11] X. H. Zhang, Z. Wang , X. Sun, , et al: Materials Letters Vols. 62 (2008) pp.4360-4362.

Google Scholar

[12] Th. Seyller: J. Phys. Cond. Matter. Vol. 16 (2004), p. S1755.

Google Scholar