The role of Cr in promoting protective alumina scale formation by γ-based Ti_Al_Cr alloys—I. Compatibility with alumina and oxidation behavior in oxygen

1997 ◽  
Vol 45 (6) ◽  
pp. 2357-2369 ◽  
Author(s):  
M Brady
2004 ◽  
Vol 12 (2) ◽  
pp. 165-180 ◽  
Author(s):  
G.S Fox-Rabinovich ◽  
G.C Weatherly ◽  
D.S Wilkinson ◽  
A.I Kovalev ◽  
D.L Wainstein

2003 ◽  
Vol 91 (7-8-9) ◽  
pp. 63-69 ◽  
Author(s):  
D. Naumenko ◽  
V. Kochubey ◽  
J. Le Coze ◽  
L. Niewolak ◽  
L. Singheiser ◽  
...  

2009 ◽  
Vol 73 (1-2) ◽  
pp. 233-253 ◽  
Author(s):  
J. Engkvist ◽  
S. Canovic ◽  
K. Hellström ◽  
A. Järdnäs ◽  
J.-E. Svensson ◽  
...  

1990 ◽  
Vol 5 (11) ◽  
pp. 2445-2450 ◽  
Author(s):  
Rao R. Nimmagadda ◽  
A. Joshi ◽  
W. L. Hsu

Oxidation kinetics of microwave plasma assisted CVD diamond and diamond-like carbon (DLC) films in flowing oxygen were evaluated in the temperature range of 500 to 750 °C and were compared with those of graphite and natural diamond. The diamond and DLC films were prepared using CH4/H2 ratios of 0.1, 0.25, 0.5, 1.0, and 2.0%. The films deposited at 0.1% ratio had a faceted crystalline structure with high sp3 content and as the ratio increased toward 2%, the films contained more and more fine crystalline sp2 bonded carbon. The oxidation rates were determined by thermal gravimetric analysis (TGA), which shows that the films deposited at ratios of 2, 1, and 0.5% oxidized at high rates and lie between the rates of natural diamond and graphite. The oxidation rate decreased with lower CH4/H2 ratio and the films deposited at 0.25 and 0.1% exhibited the lowest oxidation rates associated with the highest activation energies in the range of 293–285 kJ/mol · K. The oxidation behavior of microwave plasma assisted diamond films was similar to that of DC plasma assisted CVD diamond films. The results suggest that the same mechanism of oxidation is operational in both DC and microwave plasma assisted diamond films and is probably related to the microstructure and preferred orientation of the crystallites.


2011 ◽  
Vol 94 ◽  
pp. s146-s153 ◽  
Author(s):  
Arthur H. Heuer ◽  
David B. Hovis ◽  
James L. Smialek ◽  
Brian Gleeson

1996 ◽  
Vol 438 ◽  
Author(s):  
Y. Cheong ◽  
H. Du ◽  
S. P. Withrow

AbstractThe role of aluminum in negating the adverse effect of alkali species on the oxidation resistance of Si3N4 ceramics was investigated by exposing unimplanted and aluminum-implanted (1 and 5 at.%) Si3N4 samples to a sodium nitrate (95 ppm)-dry oxygen gas mixture at 1. atm and at 900°1100°C. Oxidation of unimplanted Si3N4 was rapid and linear with an activation energy of 57 kJ/mol. In contrast, samples implanted with aluminum exhibited a considerably reduced oxide growth which was parabolic in nature with activation energies of 103–112 kJ/mol. The morphological characteristics of the oxide layer also showed marked improvement as the aluminum concentration increased.


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