Cui
X. X., Zhang N., Kanno A., Morozumi S. Mechanical
Properties of Silicon Carbide Joints Bonded with Titanium Foil
// Nippon Kinzoku Gakkaishi - 1992. - 56(12). - 1463-1469. (Japanese).
Pressureless-sintered SiC joints, bonded at
various temps. with thin Ti foils were examd. for bend strength at
room and high temps., thermal shock resistance, oxidn. resistance
of interfacial reaction layer, and microstructure by optical microscopy
and SEM with electron probe microanal. The optimum joining temp. range
is 1773-1873 K. The bend strength at room temp. is maintained to .apprx.1473
K. The thermal shock resistance of the interfacial reaction layer
is higher than that of the bulk SiC. The interfacial reaction layer
is Ti3SiC2 which is (Si, Ti)O2 at the exposed
surface when the joint is kept at high temps. in ambient oxidizing
atm. This oxidn., however, results in strengthening of the layer by
exposure at .apprx.1473 K and then in deterioration of the layer at
>1673 K where the oxidn. of the layer proceeds rapidly.
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Gadalla
A., Elmasry M., Kongkachuichay P. High Temperature
Reactions within SiC - Al2O3
Composites
// J. Mater. Res. - 1992. - 7(9). - 2585-2592.
Composites of SiC-Al2O3
and SiC-mullite are unstable at high temperatures. The reactions occurring
within the composites between 1700 and 1850 °C in stagnant inert atmospheres
were characterized. Gaseous products cause excessive weight losses
which cannot be attributed to passive oxidation. These losses can
be successfully retarded by processing under high pressures. Compatible
phases were determined by X-ray analysis for mixtures lying in the
section SiC-Al4C3-Al2O3-SiO2.
The reactions produced condensed phases of Al2OC and Al4O4C
as well as gaseous SiO and CO. The condensed phases have high vapor
pressures above 1700 °C. The effect of these reactions on densification
of composites by firing at different temperatures for various periods
under different pressures was studied. Dence materials prepared under
high pressures at 1825 °C were tested at 1700 °C under normal pressure
in argon, where active oxidation is expected, and weight losses were
insignificant.
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Hall
I. W., Lirn J. L., Lepetitcorps Y., Bilba K. Microstructural
Analysis of Isothermally Exposed Titanium / Silicon Carbide
// J. Mater. Sci. - 1992. - 27(14). - 3835-3842.
[no
abstract]
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Lis J., Pampuch R., Stobierski L. Reactions during
SHS in a Ti-Si-C System // Int. J. Self-Propag. High-Temp.
Synth. - 1992. - 1(3). - 401-408.
The reactions and phase transitions in a Ti-Si-C
system under self-propagating high-temp. synthesis (SHS) conditions
were elucidated. The exptl. detd. phase compn. of SHS solid products
was compared with that predicted to occur at equil. The adiabatic
temp. for the initial chem. compn. of the reactants was calcd. This
temp. served as a qual. measure of the actual temp. and thus of the
probability of liq. phase formation. The SHS phase compn. from reactive
mixts. of various compn. can be explained by (i) formation of large
amts. of liq. phase with chem. compn. similar to that of the initial
mixts. for samples with a high (2900-3050 K) adiabatic temp. and (ii)
depletion of Ti and C in the liq. phase which forms in the late stages
of SHS due to the TiC solid-state reaction in the early stages of
SHS for samples with moderate (1980-2250 K) adiabatic temps.
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Oscroft
R. J., Thompson D. P. Influence of Oxygen on
the Formation of Aluminum Silicon Carbide // J. Am. Ceram.
Soc. - 1992. - 75(1). - 224-226.
X-ray diffraction studies have been used to
follow the formation of Al4SiC4 from Al4C3
and SiC and the role played by impurity oxigen. The phase Al2OC
forms in the early stages of reaction and reacts with SiC at ~1700
°C to produce Al4SiC4 plus a small amount of
an aluminosilicate liquid. This liquid dissociates at higher temperatures,
the resulting evolution of masses hindering complete densification.
Higher densities are obtained on hot-pressing.
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Oscroft
R. J., Thompson D. P. High-Temperature Reactions
in the Boron-Aluminum-Silicon-Nitrogen-Carbon System / Int.
Symp. Ceram. Mater. Compon. Engines, 4th. - Elsevier: London, 1992.
- 172-179.
The
incorporation of nitrogen into boron carbide was investigated. At
temperatures in the range 800-1100 °C , the soly. is ~3.8%. At these
and higher temps., there is a competing reaction whereby the B4C
structure is broken down and an amorphous B-N-C product is formed.
This resists crystn. even at temperatures as high as 1500 °C. Oxygen
is always present as a surface layer on carbide and nitride powders
used in high-temperature reactions. Its role in the densification
of nitrogen ceramics is well known; the present work describes its
role in the formation and densification of Al4SiC4
ceramics.
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Sambasivan S., Petuskey W. T. Phase Relationship in the
Ti-Si-C System at high Pressures // J. Mater. Res. - 1992.
- 7(6). - 1473-1479.
The compatibility of phases in the TiSiC
system was studied for pressures from 10 to 20 kbars (1 to 2 GPa)
and temperatures from 1200 °C to 1500 °C via an interfacial reaction
between titanium and silicon carbide. The interface was characterized
by backscattered electron imaging and electron probe microanalysis.
Ti3Si was stabilized at high pressures exhibiting an appreciable
solubility for carbon (up to 9 at. %). At higher temperatures and
lower pressures, it decomposed to Ti5Si3, Ti(Si,C),
and TiCx according to the relation Ti3Si(Cz)
= (0.70588)TiCx + (0.32437)Ti5Si3
+ (0.67227)Ti(Si,C), where the mathematical coefficients were calculated
using z = 0.4 and x = 0.5. No detectable quantities of carbon dissolved
in Ti5Si3 under these conditions. A clapeyron
slope of 0.08 ( 60.01) kbar/K was measured for this reaction. The
microstructure of the reaction zone and other general thermodynamic
and kinetic characteristics are discussed for different experimental
conditions.
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Yano
T., Kato S., Iseki T. High-Resolution Electron
Microscopy of the Silicon Carbide / Aluminum Carbide Interface
// J. Am. Ceram. Soc. - 1992. - 75(3). - 580 - 586.
The interface of single-crystal SiC and Al
brazed at 1273 K is investigated by high-resolution electron microscopy.
The orientation relationship of SiC to the Al4C3
reaction layer that forms between the SiC and the Al can be expressed
as (0001)SiC || (0001)Al4C3 and
[1-100]SiC || [1-100]Al4C3. Furthermore, a very
thin (two tetrahedral layers thick) transition phase and misfit dislocations
are observed between the SiC and Al4C3 lattices.
The structure of the transition phase is discussed based on the high-resolution
electron microscopy, the stacking of the (Al, Si)C4 tetrahedral
layers, and the charge balance. The same reaction product, with the
same orientation relationships, is observed at the interface of a
polycrystalline SiC and Al brazed joint.
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