Sintering of 6H(α)-SiC and 3C(β)-SiC powders with B4C and C additives
Source abstract
Abstract
The sintering behavior of three fine industrial SiC powders (two 6H(α)-type and one 3C(β)-type) has been comparatively investigated. The powders were pressureless sintered with B4C and C additives between 1950°C and 2250°C in a high temperature dilatometer with flowing Ar atmosphere. The densification and shrinkage rate curves, polytype content, and grain growth were correlated with physical and chemical characteristics of starting powders. One of 6H(α)-type powders presented good sinterability only after extensive milling, even though it presented small average particle size, narrow particle size distribution and high specific surface area. The main difference in densification behavior among powders was the narrower shrinkage rate curve of β-SiC powder, with its maximum shifted to higher temperature. Grain growth and phase transformation simultaneously occurred. In α-SiC, 6H polytype partially transformed to 4H. This transformation was favored by aluminum impurity and resulted in a microstructure with more elongated grains. In β-SiC, 3C transformed mainly to 6H, 15R and 4H, introducing many stacking faults which resulted in elongated SiC grains.
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Research context
OpenAlex topics: Advanced ceramic materials synthesis · Aluminum Alloys Composites Properties · Advanced materials and composites
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References (13)
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1. S. PROCHAZKA, in Proceedings of the 6th Symposium on Special Ceramics, Stoke-on-Trent, July 1974, edited by P. Popper (British Ceram. Res. Assoc., Stoke-on-Trent, 1975) p. 171.
2. H. TANAKA, in “Silicon Carbide Ceramics I,” edited by S. Somiya and Y. Inomata (Elsevier, London, 1991) p. 213.10.1007/978-94-011-3842-0_10 ↗
3. R. M. WILLIAM, B. N. JUTERBOCK, C. R. PETERS and T. J. WHALEN, J. Amer. Ceram. Soc. 67 (1984) C–62.
4. B. W. KIBBEL and A. H. HEUER, ibid. 72 (1989) 517.10.1111/j.1151-2916.1989.tb06170.x ↗
5. W. BUCKER, H. LANDFEEMANN and H. HAUSNER, Powder Metallurgy International 13 (1991) 37.
6. Y. ZHOU, H. TANAKA, S. OTANI and Y. BANDO, J. Amer. Ceram. Soc. 82 (1999) 1959.10.1111/j.1151-2916.1999.tb02026.x ↗
7. F. F. LANGE, J. Mater. Sci. 10 (1975) 314.10.1007/BF00540356 ↗
8. N. PADTURE, J. Amer. Ceram. Soc. 77 (1994) 519.10.1111/j.1151-2916.1994.tb07024.x ↗
9. T. GRANDE, H. SOMMERSET, E. HAGEN, K. WIIK and M. A. EINARSRUD, ibid. 80 (1997) 1047.10.1111/j.1151-2916.1997.tb02945.x ↗
10. H. TANAKA and N. IYI, ibid. 78 (1995) 1223.10.1111/j.1151-2916.1995.tb08473.x ↗
11. H. TANAKA, H. N. YOSHIMURA, S. OTANI, Y. ZHOU and M. TORIYAMA, ibid. 83 (2000) 226.10.1111/j.1151-2916.2000.tb01177.x ↗
12. J. E. BURKE, ibid. 40 (1957) 80.10.1111/j.1151-2916.1957.tb12580.x ↗
13. R. L. COBLE, ibid. 45 (1962) 123.10.1111/j.1151-2916.1962.tb11099.x ↗