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Oxidation Kinetics of an Amorphous Silicon Carbonitride Ceramic
Author(s) -
Raj Rishi,
An Linan,
Shah Sandeep,
Riedel Ralf,
Fasel Claudia,
Kleebe HansJoachim
Publication year - 2001
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1151-2916.2001.tb00918.x
Subject(s) - materials science , amorphous solid , nanopore , analytical chemistry (journal) , silicon , kinetics , nanoscopic scale , scanning electron microscope , saturation (graph theory) , reaction rate constant , volume fraction , volume (thermodynamics) , porosity , nanometre , chemical engineering , mineralogy , composite material , nanotechnology , chemistry , crystallography , metallurgy , thermodynamics , physics , mathematics , chromatography , quantum mechanics , combinatorics , engineering
The oxidation kinetics of amorphous silicon carbonitride (SiCN) was measured at 1350°C in ambient air. Two types of specimens were studied: one in the form of thin disks, the other as a powder. Both specimens contained open nanoscale porosity. The disk specimens exhibited weight gain that saturated exponentially with time, analogous to the oxidation behavior of reaction‐bonded Si 3 N 4 . The saturation value of the weight gain increased linearly with specimen volume, suggesting the nanoscale pore surfaces oxidized uniformly throughout the specimen. This interpretation was confirmed by high‐resolution electron microscopy and secondary ion mass spectroscopy. Experiments with the powders (having a particle size much larger than the scale of the nanopores) were also consistent with measurements of the disks. However, the powder specimens, having a high surface‐to‐volume ratio, continued to show measurable weight gain due to oxidation of the exterior surface. The wide range of values for the surface‐to‐volume ratio, which included all specimens, permitted a separation of the rate of oxidation of the free surface and the oxidation of the internal surfaces of the nanopores. Surface oxidation data were used to obtain the rate constant for parabolic growth of the oxidation scale. The values for the rate constant obtained for SiCN lay at the lower end of the spectrum of oxidation rates reported in the literature for several Si 3 N 4 and SiC materials. Convergence in the behavior of SiCN and CVD‐SiC is ascribed to the purity of both materials. Conversely, it is proposed that the high rates of oxidation of sintered polycrystalline silicon carbides and nitrides, as well as the high degree of variability of these rates, might be related to the impurities introduced by the sintering aids.