Abstract
The behavior of three preceramic polysilazane variations during pyrolysis is discussed. These polymers consist of the monomelic units –[H2SiNCH3]-, -[CH3SiHNH]-, and -[H2SiNCH2CH3]-. Their differing pyrolytic performances are evaluated in relation to polymer structure, functional group, and pyrolytic environment.
The thermal reactivity of the different organic groups and their position on the polymer backbone drastically affect the development of the carbonaceous species in the derived ceramic products. The bonding of hydrogen groups to the polymer’s skeleton leads to different chemical configurations in the amorphous products.
Pyrolysis in ammonia results in the elimination of the carbon content regardless of the type and bonding of the polymer’s organic groups. Different chemical mechanisms are responsible for this phenomenon. The carbon removal occurs before the conversion of the organic moieties to inorganic species.
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© 1991 Springer Science+Business Media Dordrecht
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Blum, Y.D., McDermott, G.A., Hirschon, A.S. (1991). Pyrolytic Characteristics of Polysilazanes. In: Harrod, J.F., Laine, R.M. (eds) Inorganic and Organometallic Oligomers and Polymers. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-3214-5_12
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DOI: https://doi.org/10.1007/978-94-011-3214-5_12
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