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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 272 (1978), S. 433-435 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig. 1 Transmission electron micrographs of the films formed on electropolished aluminium for various times at 50A m2 in 0.4 M phosphoric acid at 298 K. #, Stripped anodic film produced in 20s, showing the non-uniform growth of the film with thicker material at the cell boundaries in an ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 10 (1976), S. 341-345 
    ISSN: 1573-4889
    Keywords: α-Al2O3 ; platinum ; oxidation ; adhesion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The influence of externally located platinum on the isothermal stability of α-Al2O3 scales formed at high temperatures has been examined. It has been observed that a nickel-base alloy forms an external scale of α-Al2O3 during oxidation at 1200°C, but this scale breaks down isothermally, enabling a faster-growing Cr2O3-rich scale to develop. However, in the presence of platinum metal alongside the specimen in the furnace hot zone, the breakdown of the α-Al2O3 scale is postponed for a substantial period of time. It appears that platinum, as the volatile species PtO2, is incorporated into the growing α-Al2O3 scale where it either influences the stress relief mechanism at temperature or reduces oxidation growth stress generation and thus significantly enhances the isothermal stability of the scale.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-4889
    Keywords: alloy oxidation ; Ni-Cr alloys ; diffusion ; depletion zones
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Compositional changes in the alloy beneath scales have been examined for the oxidation of Ni-27.4%Cr and Ni-40.2% Cr in 1 atm oxygen in the temperature range 1073–1473°K. Calculations of the rate of approach of the interfacial alloy composition to a constant value are compared with experimental data. Theoretical chromium depletion profiles obtained using both a finite difference analysis and an analytical expression are shown to be essentially equivalent and in good agreement with experimental measurements. The consequences of alloy depletion for the scaling behavior, when the protective scale is ruptured, are discussed.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 9 (1975), S. 215-223 
    ISSN: 1573-4889
    Keywords: cation diffusion ; oxidation ; metal partition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract An alternative mass balance at the alloy-scale interface is proposed for the Wagner theory of binary alloy oxidation. A simple relation between the bulk composition of the alloy and the scale composition at the alloy-scale interface, ξ′, is derived in terms of the transport properties of the scale and the limit of application of the relation defined. There is good agreement between calculated and measured values of ξ′.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 9 (1975), S. 473-496 
    ISSN: 1573-4889
    Keywords: nickel ; sulfidation ; multilayer scale ; diffusion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The reaction between pure nickel and sulfur vapor has been studied over the temperature range 380–475° C. A scale consisting of four separate layers is formed and the growth of the three outer layers obeys parabolic kinetics. The innermost layer grows only in the very early stages, after which the thickness remains approximately constant. The layers have been identified as three different sulfides-Ni3S2, which forms the two inner layers, Ni7S6, and NiS. The three outer layers grow with preferred orientations; growth of the Ni3S2 and NiS layers is with the basal planes of their hexagonal structures parallel to the nickel substrate. The formation of the scale can be described in terms of a diffusion-controlled process and the same basic process continues after scale-metal separation occurs. The description of scale growth is combined with experimental data to calculate the diffusion coefficient of nickel ions in each phase.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 10 (1976), S. 163-187 
    ISSN: 1573-4889
    Keywords: alumina ; growth mechanism ; scale adhesion ; yttrium
    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 behavior of an Fe-27%Cr-4%Al alloy and similar alloys containing 0.023% and 0.82% Y in 1 atm oxygen at 1200°C has been examined. The oxide formed on the yttrium-free alloy develops a highly convoluted configuration, apparently resulting from lateral growth of the oxide. The latter leads to oxide detachment from the alloy at temperature and extensive spalling during cooling. It is postulated that lateral growth results from the formation of oxide within the existing oxide layer by reaction between oxygen diffusing inward down the oxide grain boundaries and aluminum diffusing outward through the bulk oxide. Additions of yttrium to the alloy apparently prevent the formation of oxide within the oxide layer, the oxide-forming reaction occurring as the alloy-oxide interface. Thus lateral growth is prevented and spalling during cooling does not occur. Secondary advantages conferred by the addition of 0.82% Y to the alloy are the prevention of void formation at the alloy-oxide interface, the avoidance of alloy grain growth during oxidation, and the creation of an oxide “keying” or “pegging” effect.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 11 (1977), S. 109-125 
    ISSN: 1573-4889
    Keywords: nickel-vanadium ; oxidation
    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 behavior of nickel and dilute Ni-V alloys has been studied in flowing oxygen at 1 atm pressure, using various kinetic and electron-optical techniques. The oxidation rate rises progressively as the alloy vanadium content is increased from 0 to 0.8% and then to 1.7%. However, further additions to 4.2% cause only a slight further increase. These increases in oxidation rate are largely controlled by the extent of doping of the NiO, particularly for the two more dilute alloys, although internal oxidation, spinel blocking effects in the oxide, and dissociation of the NiO affect the weight gains to some extent, particularly for the case of the Ni-4.2% V alloy.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 11 (1977), S. 163-191 
    ISSN: 1573-4889
    Keywords: cobalt-chromium ; oxidation ; oxygen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The isothermal oxidation of Co-Cr alloys containing 0–30% Cr in 760 Torr oxygen at 1000° C has been studied kinetically and by appropriate physical techniques. Chromium additions to cobalt increase the parabolic oxidation rate to an almost constant level from 2 to 15% Cr, while further additions to 20–30% Cr decrease the rate. All the alloys produce a virtually pure CoO layer outside a layer containing Co-Cr spinel particles in a Cr3+ -doped CoO matrix. The variation of oxidation rate with alloy chromium content is explained in terms of the complex interplay of doping, blocking of cation transport by voids and spinel particles and short circuiting by transport of dissociative oxygen across these voids and other processes, internal oxidation making a negligible direct contribution to weight gain. Complete spinel layers are never quite developed under the conditions studied, although formation of spinel does slow the oxidation rate. The improved protection eventually obtained at higher chromium levels is produced by the tendency to form a Cr2O3 healing layer.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-4889
    Keywords: nickel alloys ; cobalt alloys ; oxidation rate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Oxidation of nickel- and cobalt-base alloys, containing small additions of a higher valent second metal, in oxygen or air at high temperatures results in the formation of relatively complicated scale morphologies which change subtly with increasing additions of the second element and its characteristics. The various factors that can influence the oxidation behavior of such alloys are assessed and correlated with the oxidation kinetics and scale morphology types. For very dilute alloys the increase in oxidation rate compared with that of the corresponding pure metal (nickel or cobalt) is largely due to doping of the external oxides. However, once the solubility limit of the second metal in this oxide is exceeded, additional increases in second metal content of the alloy can either increase further or decrease the oxidation rate. The exact behavior depends on the relative interplay of factors such as internal oxide formation and coalescence, blocking effects of incorporated internal oxide or pores in the scale, short-circuit paths through the scale, doping, and the relative diffusion rates of the two metals in the scale. Probable rate-determining steps for oxidation of different alloy composition ranges are proposed.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-4889
    Keywords: alloy oxidation ; diffusion ; alloy depletion profiles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The assumptions involved in Wagner's original treatment of alloy depletion profiles are examined and found to be acceptable for many situations. Finite difference analyses do not result in profiles which are significantly different from those obtained by the much simpler analytical solution once steady-state parabolic growth is established. Consequently an analytical solution is preferred and its combination with the classical Wagner expression for scale growth leads to a unified description of alloy oxidation when only the least noble metal is oxidized. The description is tested for an Fe-27.4wt.% Cr alloy oxidized at 1273°K and agreement between theoretical and experimental results is satisfactory. Alternative treatments of alloy oxidation which require that there be no recession of the alloy-scale interface are discussed and it is concluded that this assumption is unnecessarily restrictive in many cases. Suggestions that the oxidation of austenitic steels is controlled by diffusion in the alloy and that an interfacial transfer step is of importance in determining the oxidation rate in some cases are shown to be based on invalid assumptions. An analytical solution to the diffusion equation is developed for the case when a phase change occurs in the alloy because of less noble metal depletion and an expression is also presented for the profile developed in the limiting case where depletion is determined by scale evaporation.
    Type of Medium: Electronic Resource
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