In-situ production and microstructures of iron aluminide TiC composites

被引:64
作者
Ko, SH [1 ]
Hanada, S [1 ]
机构
[1] Tohoku Univ, Inst Mat Res, Sendai, Miyagi 9808577, Japan
关键词
intermetallic; miscellaneous; iron aluminides; based on Fe3Al; heat treatment; melting; microstructure;
D O I
10.1016/S0966-9795(99)00002-3
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 [物理化学]; 081704 [应用化学];
摘要
In this study we have tried to produce the titanium carbide reinforced iron aluminide composites by in-situ reaction between titanium and carbon in liquid iron-aluminum alloy doped with titanium and carbon. A homogeneous distribution of titanium carbide particles in the iron aluminide matrix up to about 16 vol% of titanium carbide was intended without agglomeration. The composition of TiC formed during in-situ reaction was investigated by ICP analysis and the Combustion-Infrared Absorption method after chemical dissolution of the iron aluminide matrix. It is found that the composition of titanium carbide formed during melt processing is an average of Ti-48.4 mol% C. In addition, titanium carbide has very low solubility of Fe and Al. The microstructure of composites consists of three different regions; primary large TIC particles of 5-40 mu m, matrix with small dendritic TiC particles of about 1 mu m and particle-free regions around primary large TIC particles. The formation of this complex microstructure can be explained by assuming the Fe3Al-TiC pseudo-binary system containing the eutectic reaction. Particle-free regions are halos of iron aluminide phase and the formation of halos is explained by coupled zone concept. Subsequent heat treatment at 1373 K for 48 h induces spheroidization and/or coarsening of small TIC particles, while microstructure after heat treatment at 973 K for 48 h exhibits the additional formation of small TiC precipitates. Though excess 1 mol% Ti addition over the Ti content for TiC formation is soluble to Fe-28 mol% Al, excess 1 mol% C addition forms the secondary Fe3AlC phase during melt processing. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:947 / 955
页数:9
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