scholarly journals Gold Alloys for Resin Bonding including Small Amount Base Metals. Structural Changes of Alloy Surface by the High-temperature Oxidation.

1999 ◽  
Vol 18 (4) ◽  
pp. 366-384 ◽  
Author(s):  
Masahiro SAGARA ◽  
Hiroki OHNO
2011 ◽  
Vol 696 ◽  
pp. 63-69 ◽  
Author(s):  
Shigenari Hayashi ◽  
Isao Saeki ◽  
Yoshitaka Nishiyama ◽  
Takashi Doi ◽  
Shoji Kyo ◽  
...  

Very thin Fe-coatings, ~50nm, were found to suppress metastable Al2O3 formation on Fe-50Al and Ni-50Al alloys in our previous study. The authors proposed a mechanism whereby α-Al2O3 precipitates from the Al-saturated Fe2O3, which was formed during initial oxidation, since α-Al2O3 and α-Fe2O3 have isomorphous structures. In order to confirm the proposed mechanism, in-situ measurements were made of structural changes in the oxide scales formed on FeAl with and without Fe coating during heating and subsequent isothermal high temperature oxidation by synchrotron radiation with a two-dimensional X-ray detector. Diffraction peaks from Fe2O3 were initially observed at around 350°C on Fe-coated samples. The lattice parameter of the Fe2O3 initially increased linearly due to thermal expansion, but then rapidly decreased due to the formation of a solid solution of Fe2O3-Al2O3. α-Al2O3 started to appear at around 800°C, but no peaks from metastable Al2O3 were observed. The diffraction peaks from the α-Al2O3 on Fe-coated samples consisted of two distinct peaks, indicating that the α-Al2O3 had two different lattice parameters. These results suggest that the α-Al2O3 was formed not only by precipitation from the Al-saturated Fe2O3, but also by oxidation of Al in the substrate.


2017 ◽  
Vol 90 (1-2) ◽  
pp. 27-42 ◽  
Author(s):  
Richard P. Oleksak ◽  
Casey S. Carney ◽  
Gordon R. Holcomb ◽  
Ömer N. Doğan

1983 ◽  
Vol 62 (6) ◽  
pp. 774-779 ◽  
Author(s):  
H. Ohno ◽  
Y. Kanzawa ◽  
I. Kawashima ◽  
N. Shiokawa

Changes in the morphology of the oxidation zone and the quantities of oxide for gold alloys containing two base metals (In and Sn) were investigated by exposing alloys at 1000°C for one h in air. The contents of In and Sn were varied in the range of from 0-1.5 wt%. In the range of from 1.5-0,35 wt% In (from 0-1.15 wt% Sn), In2 O3 was formed predominantly at the alloy surface. The electron probe x-ray micro-analyzer detected no uniform external oxidation zone. A mixture composed of In2O3 and SnO2 precipitated internally in the alloy matrix. An external oxidation zone composed of SnO2 was formed on the alloys containing over 1.2 wt% Sn, and no internal oxidation zone was observed.


Author(s):  
I. G. Wright ◽  
V. K. Sethi ◽  
V. Nagarajan

The rate of wastage of an alloy surface subjected to erosion under conditions where high-temperature oxidation can occur can be significantly greater than that arising from erosion alone. This is because the erosion conditions can act to accelerate the oxidation process by causing regular shedding of the otherwise protective oxide scale. It is suggested that an important parameter in determining the rate of erosion-oxidation is the erodent flux, since the time available for oxide growth (or regrowth) in a given area is determined by the interval between successive erodent impacts. Using this simple premise, an approach is suggested by which the rate of erosion-oxidation can be related to the factors that control the alloy oxidation process, and those that describe the erosive environment. The assumptions made are examined, and some of the implications of this approach are discussed.


1991 ◽  
Vol 113 (4) ◽  
pp. 616-620 ◽  
Author(s):  
I. G. Wright ◽  
V. K. Sethi ◽  
V. Nagarajan

The rate of wastage of an alloy surface subjected to erosion under conditions where high-temperature oxidation can occur can be significantly greater than that arising from erosion alone. This is because the erosion conditions can act to accelerate the oxidation process by causing regular shedding of the otherwise protective oxide scale. It is suggested that an important parameter in determining the rate of erosion-oxidation is the erodent flux, since the time available for oxide growth (or regrowth) in a given area is determined by the interval between successive erodent impacts. Using this simple premise, an approach is suggested by which the rate of erosion-oxidation can be related to the factors that control the alloy oxidation process, and those that describe the erosive environment. The assumptions made are examined, and some of the implications of this approach are discussed.


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