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  • 1
    ISSN: 1573-4889
    Keywords: selective oxidation ; binary alloys ; two-phase alloys
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The conditions for the transition from the formation of mixed scales to the exclusive oxidation of the component B, forming the most stable oxide, are examined for both single-phase and two-phase binary A-B alloys by taking into account the displacement of the alloy-scale interface due to the growth of the protective oxide. This procedure eliminates the inconsistencies arising from Wagner's classical treatment for single-phase alloys when the interdiffusion coefficient in the alloy is small with respect to the parabolic rate constant for outer-scale growth; but the same procedure leads to a significantly-improved treatment also for two-phase alloys. For the latter systems, the transition is shown to depend also on the solubility of B in the A-rich phase.Moreover, the exclusive growth of the most-stable oxide is more difficult than for single-phase alloys because it requires higher average concentrations of B in the alloy and may even become impossible if the parabolic rate constant of oxidation is large with respect to the interdiffusion coefficient in the alloy.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 39 (1993), S. 197-209 
    ISSN: 1573-4889
    Keywords: oxidation ; binary alloys ; two-phase alloys
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The corrosion behavior of binary, two-phase alloys is considered in which the matrix contains mostly the less-noble metal that forms a fast-growing oxide, while the second phase is rich in a component that forms a more stable but slowly-growing oxide. It is assumed that the second phase exists as a dispersion of isolated, rod-like particles. It is further assumed that both phases form external films with no internal oxidation. It is shown that the oxidation behavior of this type of alloy depends on both the oxidation time and the size of the second-phase particles. In particular, for short oxidation times and large second-phase particles the matrix will oxidize faster than the dispersed phase, so that the dispersed particles will be only partly corroded or even incorporated into the matrix-oxide scale as unoxidized islands, forming an irregular alloy-scale interface. On the contrary, for long times and small particle sizes the two phases will tend to oxidize at approximately the same rate, leading to the formation of regular alloy-scale interfaces. The time for the transition between the two corrosion regimes depends not only on the ratio between the rate constants for the growth of the two oxides but also on the size of the dispersed-phase particles, smaller sizes producing shorter transition times. Eventually, under favorable conditions the formation of the fast-growing oxide may even stop, leading to the formation of a protective layer of the most-stable oxide.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-4889
    Keywords: oxidation kinetics ; protective scales ; binary alloys
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract During the growth of the most-stable oxide BO v in the oxidation of binary alloys containing nonnoble components A and B, the oxygen pressure prevailing at the alloy-scale interface is higher than the corresponding value for equilibrium between BO v and pure B. The effects of this change on the rate constant for the growth of BO v and on the critical concentration of B in the bulk alloy required for the stability of BO v on its surface are examined and discussed. The general treatment is then applied to the growth of NiO on Cu−Ni alloys and of Cr2O3 on Fe−Cr, Co−Cr, and Ni−Cr alloys by using appropriate defect models for these oxides, considering also the possibility of oxide doping.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 48 (1997), S. 357-380 
    ISSN: 1573-4889
    Keywords: chromium ; copper ; binary alloys ; two-phase alloys ; oxidation ; high temperatures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The oxidation in air of three two phase Cu-Cr alloys with nominal Cr contents of 25, 50, and 75 wt. % was studied at 700–900°C. The alloys corroded nearly parabolically, except at 900°C, when the corrosion rates decreased with time more rapidly than predicted by the parabolic rate law. The corrosion rate decreased for higher Cr contents in the alloy under constant temperature and generally increased with temperature for the same alloy composition. The scales were complex and consisted in most cases of an outermost copper oxide layer free from chromium and an inner layer composed of a matrix of copper oxide or of the double oxide Cu2Cr2O4, often containing particles of chromium metal surrounded by chromia and then by the double oxide. Metallic copper was also frequently mixed with chromia. Cr-rich regions tended to form continuous chromia layers at the base of the scale, especially at the highest temperature. No chromium depletion was observed in the alloy.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-4889
    Keywords: binary alloys ; two-phase alloys ; oxidation ; high temperatures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The conditions for the exclusive oxidation of the most-reactive component during the corrosion of binary, two-phase alloys by a single oxidant are reexamined by using a more correct form of the mass balance for this component. Moreover, the previous treatment is extended to include the case in which the transition falls in the range of alloy compositions corresponding to the stability of the single phase rich in the most-reactive component. The limiting conditions for the transition in the single and two-phase fields are examined and discussed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 47 (1997), S. 355-380 
    ISSN: 1573-4889
    Keywords: internal oxidation ; binary alloys ; two-phase alloys
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The internal oxidation of two phase binary A-B alloys by a single oxidant at high temperatures, under partial pressures sufficient to also form external scales of the less-stable oxide, is examined by means of quantitative models and compared with the corresponding behavior of single-phase alloys. It is shown that, depending on various factors, particularly on the solubility and diffusivity of the most-reactive component B in the most-noble component A, this process may or may not involve a diffusion process of the alloy components, leading to different scale morphologies. It is also concluded that even when the solubility and diffusivity of B in A are sufficiently high, so that the internal oxidation of the common type occurs, the restriction to the diffusion of B in the alloy due to its limited solubility affects the kinetics of internal oxidation, producing an increase of the rate of internal oxidation and of the critical concentration of B in the alloy required for the transition to the external oxidation of B with respect to single-phase alloys under the same values of all the relevant parameters. The lower the solubility of B in A, the larger these effects.
    Type of Medium: Electronic Resource
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