Silicon carbide (SiC) is an industrially important non-oxide ceramic with an attractive combination
of chemical stability, thermal fatigue resistance, high stiffness, and low density. Additionally,
production of high toughness, near-net-shape, SiC/SiC composite structures is possible through
liquid silicon (Si) melt infiltration into a SiC/carbon porous preform. Owing to a unique
combination of properties, these composites have gained interest for applications such as gas
turbines, heat shields, and automotive parts. However, dissolution of SiC into pure liquid Si is
possible during infiltration leading to undesirable and inconsistent mechanical properties.
Understanding the physicochemical interactions between SiC and Si-bearing liquids is necessary
to mitigate the dissolution of SiC during the infiltration process.
An experimental high-temperature apparatus was constructed to allow for precise vertical
translation and rotation of SiC samples under a controlled atmosphere. Utilizing the apparatus,
single crystal SiC wafers were immersed and rotated in Si melts of varying compositions to
observe the rate-controlling mechanisms for dissolution. Careful attention was placed on
maintaining precise melt composition allowing only fused silica and SiC to come in contact with
the Si melts. Experimental results confirmed the rate controlling mechanism at 1450°C as being
C transport away from the SiC/Si interface for the dissolution of single crystal 4H SiC in high?purity liquid Si. Values for the effective C solubility in high-purity Si melts were found to be
between 66 and 119 ppmw, and effective diffusion coefficients for C in high-purity liquid Si were
found to be between 8.1x10-6 and 1.3x10-4 cm2
/s. Similar experiments rotating single crystal 4H
SiC wafers in 3 wt% B – containing Si melts were performed with the rate-controlling mechanism
found to also be carbon transport away from the reaction interface. The effective C solubility in
3 wt% B- containing Si melts was found to be 94-173 ppmw and effective diffusion coefficients
for C in 3 wt% B- containing Si liquid were found to be between 4.7x10-6 and 2.1x10-4 cm2
/s.
Static immersion was also conducted on polycrystalline SiC samples prepared via hot pressing.
Immersion studies revealed a relatively slow weight loss regime at short immersion times followed
by an increased weight loss regime resulting from SiC grain fallout. Increased dissolution of
polycrystalline SiC samples was observed after immersion in Si melts containing elements known
to increase the C solubility in liquid Si and decreased dissolution was observed after immersion in
Si melts containing elements known to decrease C solubility.