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Journal Article

Citation

Bronson A, Ma YT, Mutso RR, Pingitore N. Journal of the Electrochemical Society 1992; 139(11): 3183-3196.

Copyright

(Copyright © 1992)

DOI

10.1149/1.2069052

PMID

unavailable

Abstract

At 2073 K, the compatibility couple of HfO2-4 weight percent (w/o) Y2O3/HfSi2/HfB2-5 w/o HfSi2/HfO2-4 w/o Y2O3(symbolized as O/Si/B/O) shows that the Hf-Si-0 system is complicated by the existence of a two-liquid region in the HfO2-SiO2-HfSi2-Hf2Si pseudoquaternary phase diagram. The diffusion of the oxide ion through the silicate liquid phase appears to control the development of product phases between the HfO2 and HfSi2 phases at 2073 K. In addition, the reaction product consists of two liquid phases, silicate and silicide, between the HfO2 and HfSi2 phases. In the formation of the two liquids, the hafnium ions partition into the suicide phase leaving the silicate anions to polymerize and form complicated silicate rings which establishes the free oxide ion activity. Hafnium boride was determined to be relatively inert to either the oxide and silicide phase when examined with an optical microscope, scanning electron microscope, and electron microprobe. At 1873 K, the compatibility couple of O/Si/B/O showed no measurable movement of the oxide/silicide interface and suggests that a stable solid-solid immiscibility of HfSi2 and HfO2 exists. The immobility of the interface also suggests that a liquid is necessary for the interfacial reaction to occur and dissolve hafnia. © 1992, The Electrochemical Society, Inc. All rights reserved.


Language: en

Keywords

High temperature effects; Ceramic materials; Metallic compounds; Borides; Composite materials; Metal borides; Metal oxides; Oxides; Refractory materials; Refractory metal borides/oxide composites; Ultrahigh temperature effects

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