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Kinetics of Thermal, Passive Oxidation of Nicalon Fibers
Author(s) -
Zhu Yuntian T.,
Taylor Seth T.,
Stout Michael G.,
Butt Darryl P.,
Lowe Terry C.
Publication year - 1998
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.1151-2916.1998.tb02386.x
Subject(s) - oxidizing agent , oxide , diffusion , thermal oxidation , kinetics , oxygen , materials science , oxidation process , redox , chemical engineering , layer (electronics) , chemical kinetics , chemistry , composite material , thermodynamics , metallurgy , physics , organic chemistry , quantum mechanics , engineering
The oxidation of Nicalon fibers is a concern, because of its potential as a reinforcement of high‐temperature composites, whose service conditions involve high‐temperature, oxidizing environments. Two limiting types of oxidation mechanisms are often used to describe the kinetics: chemical‐reaction‐controlled oxidation, at small oxide thicknesses, and diffusion‐controlled oxidation, at large oxide thicknesses. Neither mechanism can satisfactorily describe the intermediate region where the oxidation kinetics are controlled jointly by both the chemical reaction rate at the interface and the diffusion of oxygen through the oxide layer. To describe the entire oxidation process with a general relationship, one must consider all stages of the oxidation process, namely (i) adsorption of oxygen at the outer surface of the oxide, (ii) diffusion of oxygen from the outer surface toward the interface where oxidation occurs, and (iii) reaction at the interface to form a new layer of oxide. Previously, a very useful general relationship was derived for the oxidation kinetics for a flat plate, which could account for all three stages of oxidation. However, that equation is inadequate to describe the oxidation of cylindrical fibers, because the effective area for oxygen diffusion changes along the diffusion path and the oxidation interfacial area decreases as the oxide thickness increases for cylindrical fibers. In this paper, we have derived a general kinetic relationship for the oxidation of cylindrical fibers, which can account for all stages of oxidation. Comparison of the theory with experimental data of Nicalon fibers shows good agreement.