Abstract

Activated carbon fiber composites (ACFCs) with the specific surface area of about 1150 m 2/g were reacted to produce silicon carbide fiber composites with SiO vapor generated from a mixture of Si and SiO 2 at 1673 K under vacuum for various hold times ranging between 10–120 min. Chemical analysis of the converted ACFCs resulting from reaction showed that the products contained 79–90 wt.% silicon carbide, 7–13 wt.% amorphous silica and 3–8 wt.% unreacted carbon, and the composition depended on hold time. At an early stage of the SiO–C reaction during hold time, part of the excess SiO vapor generated was presumed to condense on to the converted fiber surface as amorphous silica, thereby reducing the specific surface area of the converted ACFCs. As the C–SiC conversion proceeded, the gas-phase carbon reduction of SiO 2 with CO occurred and increased the specific surface area from 25 m 2/g to 48 m 2/g. Strength of the converted ACFCs decreased with conversion due to the increased specific surface area and crack formation in the converted carbon fiber.

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