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  • two-phase alloys  (11)
  • mixed gas  (3)
  • 1
    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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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 37 (1992), S. 217-252 
    ISSN: 1573-4889
    Keywords: mixed gas ; Nb2O5 ; NiNb3S6 ; NiNb2S4 ; multi-layered scales ; oxidation ; sulfidation
    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 Ni-Nb alloys containing up to 40 wt.% Nb was studied over the temperature range of 550–800°C in a mixed H2/H2O/H2S gas. The scales formed on all alloys were multilayered. The outer scale was single-phase Ni3S2, while the structure and constitution of the inner scale depended on alloy composition and reaction conditions. Internal oxidation has been found in Ni-20Nb and Ni-30Nb, external oxidation has been observed on Ni-34Nb. Platinum markers were located at the interface between the outer scale and inner scale. The decrease in corrosion rate with increasing Nb content may be attributed to the presence of increasing amounts of Ni-Nb double sulfides as well as to the presence of Nb2O5 in the inner region of the scale.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 37 (1992), S. 413-439 
    ISSN: 1573-4889
    Keywords: mixed gas ; Ni3S2, MoS2 ; Ni2.5Mo6S6.7 ; double-layered scales ; sulfidation
    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 Ni-Mo alloys containing up to 40 wt.% Mo was studied over the temperature range of 550–800
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  • 4
    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.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 31 (1989), S. 341-367 
    ISSN: 1573-4889
    Keywords: Fe-Mo alloys ; sulfidation ; two-phase alloys ; duplex scales ; MoS2
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Iron-molybdenum alloys containing up to 40 wt.% molybdenum were exposed to sulfur vapor at a partial pressure of 0.01 atm at temperatures of 600–900°C. Sulfidation kinetics were measured over periods of up to 8 hr using a quartz-spring thermogravimetric method. The sulfidation kinetics of all alloys studied obeyed the parabolic rate law. The sulfidation rate of iron was found to be reduced by factors of 60 at 900°C and 120 at 600°C by the addition of 40 wt.% molybdenum. Duplex sulfide scales formed on all alloys at all temperatures, the scales consisting of an inner layer of mostly MoS2 and an outer layer of FeS. Platinum markers were located at the interface between the outer and inner scales, showing that outward iron diffusion and inward sulfur diffusion through the inner layer occurred. The improved sulfidation resistance was attributed to the formation of the MoS2, which acted as a partially protective barrier to the diffusion of the reacting species. Sulfidation activation energies were found to range from 24.3 to 28.5 kcal mole for the alloys compared to 20.6 kcal/mole, for pure iron. The rate-controlling step was outward iron diffusion through the outer iron sulfide layer.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 37 (1992), S. 441-461 
    ISSN: 1573-4889
    Keywords: mixed gas ; Co1.62Mo6S8 ; lamellae ; multilayered scale ; sulfidation
    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 Co alloyed with up to 40 wt.% Mo alloys was studied in H2-H2O-H2S gas mixtures over the temperature range between 600
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  • 7
    ISSN: 1573-4889
    Keywords: two-phase alloys ; oxidation ; scale structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The main possible modes of the high-temperature corrosion of binary twophase alloys by a single oxidant under gas-phase pressures sufficient to corrode both alloy components are examined to highlight the differences in their behavior with respect to single-phase alloys. It is shown that in the absence of important diffusion processes of the metal components in the alloy the expected scale structures are significantly different from those typical of single-phase alloys. The effects due to the existence of different degrees of deviation from equilibrium as a result of kinetics hindrances for the formation of the most stable oxide and in the absence of alloy diffusion are then examined. It is also shown that when diffusion in the alloy becomes important the alloy may develop an outer single-phase layer depleted in the most-reactive component, which may lead to various possible scale structures. The conditions for the transition between the various oxidation modes as well as the effect of the various parameters of kinetics, thermodynamic and structural nature over the corrosion behavior of two-phase alloys are also examined.
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  • 8
    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.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 43 (1995), S. 379-394 
    ISSN: 1573-4889
    Keywords: two-phase alloys ; oxidation ; scale structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The main possible modes of the high-temperature corrosion of binary two-phase alloys by a single oxidant under gas-phase pressures sufficient to corrode only the most-reactive alloy component are examined to compare their behavior with that of single-phase alloys. In the absence of important diffusion processes of the metal components in the alloy, the scale structures expected are different from those typical of single-phase alloys. Moreover, when diffusion in the alloy becomes important, these systems may develop an outer single-phase layer depleted in the most-reactive component, which may lead to different possible scale structures. The conditions for the transition between the various oxidation modes as well as the effect of the various parameters of kinetic, thermodynamic, and structural nature over the corrosion behavior of two-phase alloys are also examined.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 54 (2000), S. 559-574 
    ISSN: 1573-4889
    Keywords: silver–nickel ; mechanical alloying ; oxidation ; 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 Two nanophase Ni-base alloys containing 50 and 25 at.% Ag prepared by mechanical alloying, denoted Ni–50Ag and Ni–25Ag were oxidized in air at 600 and 700°C for 24 hr. Ni–50Ag underwent internal oxidation of nickel, associated with the formation of a continuous outermost layer of silver metal with scaling rates larger than those for pure nickel. On the contrary, Ni–25Ag formed a continuous NiO layer surmounted by a discontinuous silver layer and internal oxidation was suppressed. The oxidation rate of Ni–25Ag decreased with time much more rapidly than predicted by the parabolic rate law during the initial stage and eventually became parabolic, with rate constants much lower than those for the oxidation of pure nickel. These results are attributed to the two-phase nature and, particularly, to the very small grain size of the two alloys.
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