journal article·2008-06

Oxidation of SiC powders for the preparation of SiC/mullite/alumina nanocomposites

Jingyan He, Clive Brian Ponton

Journal of Materials Science· Volume 43· Issue 12
Publisher page

Abstract

The oxidation behaviour of two types of SiC powder of differing particle size and morphology distribution has been studied in the present work; one submicron-sized and the other micron-sized. It has been observed that the onset-temperature for significant oxidation of the SiC powder of smaller particle size is much lower than that for the SiC powder of larger particle size; namely, about 760 °C as compared with about 950 °C. Furthermore, the rate and extent of oxidation of the former SiC powder is much higher than that of the latter SiC powder. Interestingly, however, the SiC powder of smaller particle size exhibits more controllable oxidation behaviour in the context of the preparation of SiC/mullite/alumina nanocomposites, i.e., in terms of the extent of oxidation, and hence the amount of silica formed as an encapsulating outer layer and the resulting core SiC particle size, than the SiC powder of larger particle size. The SiO2 layer formed was amorphous when the SiC powders were oxidized below 1,200 °C, but crystalline in the form of cristobalite when they were oxidized above 1,200 °C. Since the presence of amorphous silica can accelerate the sintering of the nanocomposite, oxidation of the chosen SiC powder should thus take place below 1,200 °C.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Advanced ceramic materials synthesis · Aluminum Alloys Composites Properties · Advanced materials and composites

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (17)

Show source-provided references
1. Shi Z, Lee J, Zhang D, Lee H, Gu M, Wu R (2001) J Mater Tech 110:12710.1016/S0924-0136(00)00839-6 ↗
2. Vaughn WL, Maahs HG (1990) J Am Ceram Soc 73(6):154010.1111/j.1151-2916.1990.tb09793.x ↗
3. Ramberg CE, Cruciani G, Spear KE, Tressler RE, Ramberg CF Jr (1996) J Am Ceram Soc 79(3):730
4. Ogbuji LUJT (1997) J Am Ceram Soc 80(6):154410.1111/j.1151-2916.1997.tb03014.x ↗
5. Lin YJ, Chen LJ (2000) Ceram Int 26:59310.1016/S0272-8842(99)00102-9 ↗
6. Deal BE, Grove AS (1965) J Appl Phys 36(12):377010.1063/1.1713945 ↗
7. Opila EJ (1994) J Am Ceram Soc 77(3):73010.1111/j.1151-2916.1994.tb05357.x ↗
8. Holz D, Claussen N (1995) Ceram Eng Sci Proc 16(1):25210.1002/9780470314616.ch36 ↗
9. Wu S, Claussen N (1994) J Am Ceram Soc 77(11):289810.1111/j.1151-2916.1994.tb04521.x ↗
10. Sakka Y, Bidinger DD, Aksay IA (1995) J Am Ceram Soc 78(2):47910.1111/j.1151-2916.1995.tb08827.x ↗
11. Carter RE (1961) J Chem Phys 34:201010.1063/1.1731812 ↗
12. Liu DM (1997) Ceram Int 23:42510.1016/S0272-8842(96)00051-X ↗
13. Costello JA, Tressler RE (1986) J Am Ceram Soc 69(9):67410.1111/j.1151-2916.1986.tb07470.x ↗
14. Singhal SC (1976) J Mater Soc 29:124610.1007/BF00545142 ↗
15. Pultz WW (1967) J Phys Chem 71(13):455610.1021/j100872a067 ↗
16. Villegas M, Sierra T, Lucas F, Fernández JF, Caballero AC (2007) J Euro Cer Soc 27:861–86510.1016/j.jeurceramsoc.2006.04.041 ↗
17. Kaya C (1999) PhD thesis, University of Birmingham