Different liquid polymers in the system SiCN with tailored structures were
prepared by ammonolysis from functionalized chlorosilanes. Crosslinking to
an unmeltable polymer with initiators at low temperatures and subsequent ce
ramization were studied applying Si-29 solid-state nuclear magnetic resonan
ce (NMR) spectroscopy in combination with Fourier transformed infrared (FTI
R) spectroscopy and thermoanalytical techniques.
Microstructure development, in particular, the devitrification of the corre
sponding bulk polymer-derived SiCN glasses was investigated by scanning ele
ctron microscopy (SEM) and transmission electron microscopy (TEM). Preparat
ion of monolithic samples was performed by mixing liquid polysilazane with
SiCN-powder particles, derived from the same precursors by heat treatment a
t 300 degrees C, and subsequent annealing at temperatures exceeding 1000 de
grees C to initiate crystallization. Depending on the functionalities of th
e SiCN-precursor and the processing conditions, different microstructures w
ere obtained.
The material prepared from the HVNG precursor revealed a homogeneous amorph
ous micro structure with only a small fraction of crystallized spherical in
clusions after exposure at 1540 degrees C: for 6 h in nitrogen atmosphere.
In contrast, investigating ceramic monoliths derived from another SiCN prec
ursor, a different crystallization sequence was observed. The material deri
ved from the HPS precursor showed crystallization of large alpha-Si3N4 grai
ns within the bulk. As will be discussed in detail, devitrification of thes
e polymer-derived glasses is promoted by local rearrangements and possible
phase separations within the amorphous bulk. Moreover, local decomposition
and residual porosity can affect the crystallization behavior, which strong
ly differs depending on the polymer employed.
In addition to the crystallization phenomena observed, different oxidation
response was monitored for the two SiCN ceramics discussed here. Moreover,
fracture strength and hardness data were recorded, which, however, did not
substantially differ between the polymer-derived ceramics investigated. (C)
1999 Elsevier Science S.A. All rights reserved.