Oxidation kinetics and strength of Hi-Nicalon<sup>TM</sup>-S SiC Fiber after oxidation in dry and wet air
File(s) Ox Kinetics and Strength Hi Nic S.pdf (1.92 MB)
Accepted version
Author(s)
Hay, RS
Chater, RJ
Type
Journal Article
Abstract
Hi
-
Nicalon
TM
-
S SiC fiber
strengths
and Weibull moduli
were measured after oxidation
for up to 100 hours
between 700° and 1
400°C
in wet
and dry
air
.
SiO
2
s
cale
thickness
and crystallization extent were
measured by
T
EM.
Th
e effect of furnace e
nvironment
and bake
-
out on trace element levels in SiO
2
scales was characterized
by secondary ion mass spectroscopy (
SIMS
).
C
rystallization kinetics
and Deal
-
Grove
oxidation kinetics for
glass
and crystalline scale
, and the transition between them,
were determined
and modeled
.
Crystallization retards
oxidation kinetics, and scale that forms in the crystalline state is heavily deformed
by the growth stress
accompanying SiC oxidation volume expansion
.
Glass scales formed in dry air sli
ghtly increase
fi
ber strength.
Glass sc
ales formed in wet air do
not increase strength
,
and in some cases
significantly
decrease strength
. Scales
more than 200 nm thick were usually
partially
or completely
crystallized
,
and
these
f
ibers
had
low
strength
s
.
Contamination of s
cales by trace impurities such as
A
l
and Ca during heat
-
treatment significantly inhibited
crystallization.
The oxidation
kinetics
and the strengths of oxidized
Hi
-
Nicalon
TM
-
S fibers are compared with
results from previous stu
dies.
Empirical r
elationships between oxidation
temperature, time, scale thickness,
and
strength are
determined and
discussed.
-
Nicalon
TM
-
S SiC fiber
strengths
and Weibull moduli
were measured after oxidation
for up to 100 hours
between 700° and 1
400°C
in wet
and dry
air
.
SiO
2
s
cale
thickness
and crystallization extent were
measured by
T
EM.
Th
e effect of furnace e
nvironment
and bake
-
out on trace element levels in SiO
2
scales was characterized
by secondary ion mass spectroscopy (
SIMS
).
C
rystallization kinetics
and Deal
-
Grove
oxidation kinetics for
glass
and crystalline scale
, and the transition between them,
were determined
and modeled
.
Crystallization retards
oxidation kinetics, and scale that forms in the crystalline state is heavily deformed
by the growth stress
accompanying SiC oxidation volume expansion
.
Glass scales formed in dry air sli
ghtly increase
fi
ber strength.
Glass sc
ales formed in wet air do
not increase strength
,
and in some cases
significantly
decrease strength
. Scales
more than 200 nm thick were usually
partially
or completely
crystallized
,
and
these
f
ibers
had
low
strength
s
.
Contamination of s
cales by trace impurities such as
A
l
and Ca during heat
-
treatment significantly inhibited
crystallization.
The oxidation
kinetics
and the strengths of oxidized
Hi
-
Nicalon
TM
-
S fibers are compared with
results from previous stu
dies.
Empirical r
elationships between oxidation
temperature, time, scale thickness,
and
strength are
determined and
discussed.
Date Issued
2017-05-08
Date Acceptance
2017-02-02
Citation
Journal of the American Ceramic Society, 2017, 100 (9), pp.4110-4130
ISSN
1551-2916
Publisher
Wiley
Start Page
4110
End Page
4130
Journal / Book Title
Journal of the American Ceramic Society
Volume
100
Issue
9
Copyright Statement
This is the peer reviewed version of the following article:Hay RS, Chater RJ. Oxidation kinetics strength of Hi-NicalonTM-S SiC fiber after oxidation in dry and wet air. J Am Ceram Soc. 2017;100:4110–4130, which has been published in final form at https://doi.org/10.1111/jace.14833. This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving.
Subjects
Science & Technology
Technology
Materials Science, Ceramics
Materials Science
ceramic matrix composites
fibers
oxidation
silicon carbide
strength
SILICON-CARBIDE FIBERS
HIGH-TEMPERATURE OXIDATION
LOW-OXYGEN CONTENT
CERAMIC-MATRIX COMPOSITES
NICALON TYPE-S
THERMAL-OXIDATION
HI-NICALON
PASSIVE-OXIDATION
WATER-VAPOR
STRESS-RUPTURE
0912 Materials Engineering
0913 Mechanical Engineering
Materials
Publication Status
Published
