Hostname: page-component-78c5997874-s2hrs Total loading time: 0 Render date: 2024-11-02T20:00:26.869Z Has data issue: false hasContentIssue false

Formation of in situ Reinforced Microstructures in α-sialon Ceramics: Part II. In the Presence of a Liquid Phase

Published online by Cambridge University Press:  31 January 2011

Hong Peng
Affiliation:
Department of Inorganic Chemistry, Arrhenius Laboratory, Stockholm University, S-106 91, Stockholm, Sweden
Zhijian Shen*
Affiliation:
Department of Inorganic Chemistry, Arrhenius Laboratory, Stockholm University, S-106 91, Stockholm, Sweden
Mats Nygren
Affiliation:
Department of Inorganic Chemistry, Arrhenius Laboratory, Stockholm University, S-106 91, Stockholm, Sweden
*
a)Address all correspondence to this author. e-mail: [email protected]
Get access

Extract

In situ reinforced microstructures with well-dispersed elongated grains, up to 10 μm in length, embedded in matrices consisting of submicron equiaxed grains, were developed by hot pressing Y-, Yb-, and (Y + Yb)-doped a-sialon ceramics containing approximately 3 vol% extra liquid phase at a comparatively low sintering temperature, 1800 °C. The liquid phase, thermodynamically compatible with a-sialon, was introduced by raising the oxygen content of an already oxygen-rich α-sialon composition, e.g., by increasing the O/N ratio in RExSi12-(3x+n) Al3x+nOnN16−n. Two different α–Si3N4 precursor powders, one fine-grained and one coarse, and one coarse β–Si3N4 powder were used, and the influence of particle size and crystalline modification of the precursor Si3N4 powder on the formation of elongated a-sialon grains was investigated. The formation of elongated α-sialon grains was promoted by introducing an extra liquid phase and by using a fine-grained α–Si3N4 powder, whereas the coarse β–Si3N4 powder did not yield any elongated grains at all. The obtained in situ reinforced α-sialon ceramics were both hard and tough, with a Vickers hardness and a fracture toughness of 21 GPa and approximately 5 MPa m1/2, respectively.

Type
Articles
Copyright
Copyright © Materials Research Society 2002

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1.Shen, Z-J., Ekström, T., and Nygren, M., J. Phys. D: Appl. Phys. 29, 893 (1996).CrossRefGoogle Scholar
2.Shen, Z-J., Nordberg, L-O., Nygren, M., and Ekström, T., NATO ASI Ser., Ser. 3 (25) Engineering Ceramics ’96: Higher Realiability through Process, edited by Babini, G.N. (1997), pp. 168178.Google Scholar
3.Shen, Z-J., Peng, H., and Nygren, M., J. Mater. Res. 17, 336 (2002).CrossRefGoogle Scholar
4.Wood, C.A., Zhao, H., and Cheng, Y-B., J. Am. Ceram. Soc. 82, 421 (1999).CrossRefGoogle Scholar
5.Li, Y-W., Wang, P-L., Chen, W-W., Cheng, Y-B., and Yan, D-S., Mater. Lett. 47, 281 (2001).CrossRefGoogle Scholar
6.Zhang, C., Komeya, K., Tatami, J., and Meguro, T., J. Eur. Ceram. Soc. 20, 939 (2000).CrossRefGoogle Scholar
7.Chen, I-W. and Rosenflanz, A., Nature 389, 701 (1987).CrossRefGoogle Scholar
8.Shin, I.H. and Kim, D.J., Mater. Lett. 47, 329 (2001).CrossRefGoogle Scholar
9.Wang, C-M., Hirosaki, N., and Mitomo, M., J. Ceram. Soc. Jpn. 108, 298 (2000).CrossRefGoogle Scholar
10.Wang, P.L., Sun, W.Y., and Yen, T.S., Eur. J. Solid State Inorg. Chem. t.31, 93 (1994).Google Scholar
11.Anstis, G.R., Chantikul, P., Lawn, B.R., and Marshall, D.B., J. Am. Ceram. Soc. 64, 533 (1981).CrossRefGoogle Scholar
12.Werner, P-E., Archives for Chemistry 31, 513 (1969).Google Scholar
13.Ekström, T., Käll, P-O., Nygren, M., and Olsson, P-O., J. Mater. Sci. 24, 1853 (1989).CrossRefGoogle Scholar