SiC–SiC matrix composite

SiC–SiC matrix composite is a particular type of ceramic matrix composite(CMC) which have been accumulating interest mainly as
high temperature materials for use in applications such as gas turbines, as an alternative to metallic alloys. CMCs are generally a
system of materials that are made up of ceramic fibers or particles that lie in a ceramic matrix phase. In this case, a SiC/SiC
composite is made by having a SiC (silicon carbide) matrix phase and a fiber phase incorporated together by different processing
methods. Outstanding properties of SiC/SiC composites include high thermal, mechanical, and chemical stability while also
providing high strength toweight ratio.[1]

Contents
Processing
Properties
Mechanical properties
Thermal properties
Chemical properties
References

Processing
SiC/SiC composites are mainly processed through three different methods. However, these processing methods are often subjected to
[1]
variations in order to create the desired structure or property:

1. Chemical Vapor Infiltration (CVI) – The CVI method uses a gas phase SiC precursor to first grow SiC whiskers or
nanowires in a preform, using conventional techniques developed with CVD. Following the growth of the fibers, the
gas is again infiltrated into the preform to densify and create the matrix phase. Generally , the densification rate is
slow during CVI, thus this process creates relatively high residual porosity (10–15%). [1][2]

2. Polymer Impregnation and Pyrolysis (PIP)– The PIP method uses polymeric SiC precursors to infiltrate into a
fiberous preform to create a SiC matrix. This method yields low stoichiometry as well as crystallinity due to the
polymer-to-ceramic conversion process. Additionally , shrinkage also occurs during this conversion process, resulting
in 10–20% residual porosity. Multiple infiltrations can be performed to compensate for the shrinkage. [3]

3. Melt Infiltration (MI) – The MI method has several variations, including using a dispersion of SiC particulate slurry to
infiltrate into the fiberous preform, or using CVI to coat carbon on the SiC fibers, followed with infiltrating liquid Si to
react with the carbon to form SiC. With these methods, chemical reactivity , melt viscosity, and wetting between the
two components should be considered carefully . Some issues with infiltrating melted Si is that the free Si can lower
the composite's resistance to oxidation and creep. However , this technique usually yields lower residual porosity
(~5%) compared to the other two techniques due to higher densification rates. [1][4][5]

Properties

Mechanical properties
Mechanical properties of CMCs, including SiC–SiC composites can vary depending on the properties of their various components,
namely, the fiber, matrix, and interphases. For example, the size, composition, crystallinity, or alignment of the fibers will dictate the
properties of the composite. The interplay between matrix microcracking and fiber-matrix debonding often dominates the failure
mechanism of SiC/SiC composites. This results in SiC/SiC composites having non-brittle behavior despite being fully ceramic.
, but still dependent on its various constituents.[1][6]
Additionally, creep rates at high temperatures are also extremely low
Thermal properties
SiC–SiC composites have a relatively high thermal conductivity and can operate at very high temperatures due to their inherently
high creep and oxidation resistance. Residual porosity and stoichiometry of the material can vary its thermal conductivity, with
increasing porosity leading to lower thermal conductivity and presence of Si–O–C phase also leading to lower thermal conductivity.
[1]
In general, a typical well processed SiC–SiC composite can achieve a thermal conductivity of around 30 W/m-K at 1000 Celsius.

Chemical properties
Since SiC–SiC composites are generally sought for in high temperature applications, their oxidation resistance is of high importance.
The oxidation mechanism for SiC–SiC composites vary depending on the temperature range, with operation in the higher temperature
range (>1000 °C) being more beneficial than at lower temperatures (<1000 °C). In the former case, passive oxidation generates a
protective oxide layer wheres in the latter case, oxidation degrades the fiber-matrix interface. Nonetheless, oxidation is an issue and
[1]
environmental barrier coatings are being investigated to address this issue.

References
1. Naslain, R. R. (2005), SiC-Matrix Composites: Nonbrittle Ceramics for Thermo-Structural Application. International
Journal of Applied Ceramic Technology, 2: 75–84. doi: 10.1111/j.1744-7402.2005.02009.x
2. Yang, W.; Araki, H.; Kohyama, A.; Thaveethavorn, S.; Suzuki, H.; Noda, .T(2004). "Fabrication in-situ SiC
nanowires/SiC matrix composite by chemical vapour infiltration process".
Materials Letters. 58 (25): 3145.
doi:10.1016/j.matlet.2004.05.059(https://doi.org/10.1016%2Fj.matlet.2004.05.059) .
3. Nannetti, C. A., Ortona, A., de Pinto, D. A. and Riccardi, B. (2004), Manufacturing SiC-Fiber-Reinforced SiC Matrix
Composites by Improved CVI/Slurry Infiltration/Polymer Impregnation and Pyrolysis. Journal of the American
Ceramic Society, 87: 1205–1209. doi: 10.1111/j.1551-2916.2004.tb20093.x
4. Brennan, J. J. (2000). "Interfacial characterization of a slurry-cast melt-infiltrated SiC/SiC ceramic-matrix composite".
Acta Materialia. 48 (18–19): 4619–4628. doi:10.1016/S1359-6454(00)00248-2(https://doi.org/10.1016%2FS1359-64
54%2800%2900248-2).
5. Hillig, W. B. (1988), Melt Infiltration Approachto Ceramic Matrix Composites. Journal of the American Ceramic
Society, 71: C-96–C-99. doi: 10.1111/j.1151-2916.1988.tb05840.x
6. Hinoki, Tatsuya, Edgar Lara-Curzio, and Lance L. Snead. "Mechanical properties of high purity SiC fiber-reinforced
CVI-SiC matrix composites." Fusion science and technology 44 (2003): 211–218.

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