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  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 154 (Mar. 1994), p. 119-128 
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 251-254 (Oct. 1997), p. 723-736 
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 595-598 (Sept. 2008), p. 823-832 
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: A mechanistic model that interprets the transition in oxidation behavior of zirconiumdiboride as the temperature is varied from 600°C to 2500°C is presented. Available thermodynamicdata and literature data for vapor pressures, oxygen permeability in boria, and viscosity of boriawere used to evaluate the model. Three regimes and the temperatures of transition between themwere identified. In the intermediate temperature regime, viz., 1000ºC to 1800ºC, goodcorrespondence was obtained between theory and experiments for weight gain, recession, and scalethickness as functions of temperature and oxygen partial pressure. In this regime, the rate-limitingstep is the diffusion of dissolved oxygen through a film of liquid boria in capillaries at the base ofthe oxidation product. At lower temperatures, an external boria scale forms, but it was not found tocontribute significantly to oxidation resistance. Comparison with literature data on recession is verygood, but weight gain is predicted to be higher than experimentally observed unless flow of viscousboria is included. At higher temperatures, the boria is lost by evaporation, and the oxidation rate islimited by diffusion of molecular oxygen through the capillaries between nearly columnar blocks ofthe oxide MO2.; this regime is soon followed by a rapid acceleration of recession due tovaporization of the oxide MO2 itself
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 11 (1977), S. 193-198 
    ISSN: 1573-4889
    Keywords: oxidation ; scaling ; wustite ; magnetite ; iron
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The theory of the growth of two oxide layers by Yurek et al. has been applied to the oxidation of iron at 1100° C. The theoretical parabolic rate constants for the simultaneous growth of the two oxide layers were calculated from radioactive tracer diffusion coefficients for wustite and magnetite. Good agreement was found between the theoretical and experimental values of the ratio of scale thicknesses.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 27 (1987), S. 187-197 
    ISSN: 1573-4889
    Keywords: Grain coalescence ; wustite growth ; environmental SEM
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The growth of wustite grains during the initial stages of iron oxidation at 1050°C and $$P_{O_2 } = 10^{ - 4} $$ atm has been investigated in situ in a hot-stage environmental SEM (HSESEM). Adjacent wustite grains were seen to coalesce by annihilation of the grain boundary dislocations constituting original boundaries. Specifically, dissociation of a grain boundary into an array of dislocations followed by their annihilation either by glide or climb was observed. The grain boundaries exhibiting this coalescence are believed to be low-angle boundaries. A controlled extent of oxidation followed by rapid cooling in the HSESEM enabled the study of wustite grain boundaries. Dissociation of a grain boundary into dislocations without their annihilation was also observed in later stages of oxidation when the dislocation mobility was severely reduced.In this case, instead of grain coalescence, nucleation of a new grain with an orientation different from either of the two original grains took place.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 32 (1989), S. 89-109 
    ISSN: 1573-4889
    Keywords: cementation pack ; masteralloy ; activator ; halides ; hydrides ; thermodynamics ; diffusion coating
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The partial pressures of equilibrium gaseous species in pack-cementation diffusion processes using pure condensed Al(l), Cr(s), and Si(s) metals activated by various halide salts under Ar or reducing environments which contain different amounts of hydrogen have been calculated. The analyses indicate that the presence of hydrogen gas in the system does not significantly alter the equilibrium partial pressures of gaseous species for a pack containing Al at unit activity. In general, the partial pressures of CrCl2 and SiCl2 are higher in a chloride-activated pack than in a fluoride-activated pack. Therefore, the codeposition of Cr or Si with Al is possible when a chloride salt is used as the activator with a masteralloy of composition dilute in Al. The addition of hydrogen to the gas phase decreases the partial pressure of Cl2 and thereby the partial pressures of CrCl2 and SiCl2. However, the presence of hydrogen and the formation of hydrogen halides and metal hydrides could increase the kinetics of the transporting processes, particularly for the coatings of Cr and Si. The study also indicates that the vapor pressures for the volatile chlorides of Fe are significantly higher than those for Ni or Co, so that displacement reactions leading to the loss of Fe from the substrate are expected for coating processes involving high halide activities.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 38 (1992), S. 33-43 
    ISSN: 1573-4889
    Keywords: Pack cementation ; aluminide diffusion coatings ; metal halide vapors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract An atmospheric pressure sampling mass spectrometer was used to identify the vapor species generated in a halide-activated, cementation pack. Pack powder mixtures containing a Cr-Al binary masteralloy powder, an NH4Cl activator salt, and either ZrO2 or Y2O3 (or neither) were analyzed at 1000°C. Both equilibrium calculations for the pack and mass spectrometer results indicated that volatile AlClx and CrCly species were generated by the pack powder mixture; in packs containing the reactive element oxide, volatile ZrClz and YClw species were formed by the conversion of their oxide sources.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-4889
    Keywords: pack cementation ; codeposition ; boron-modified ; germanium-doped ; titanium silicide ; diffusion coatings ; multilayered growth kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A halide-activated, cementation pack has been developed to codeposit either silicon and boron or else silicon and germanium in a single processing/reaction step to grow Ti-silicide diffusion coatings on commercially pure (CP) titanium, Ti-22Al-27Nb, and Ti-20Al-22Nb. Since boron is nearly insoluble in TiSi2, a TiB2 layer is localized at the surface of the B-modified silicide coatings. The thickness of the TiB2 layer is controlled by the choice of boron activity and halide activator in the pack. Germanium is soluble in the Ti-silicide layers but inhomogeneously distributed in the Ge-doped silicide coating. The germanium content is controlled by choices of the Si-to-Ge ratio and the halide activator in the pack. The growth kinetics for the five-layered B-modified silicide coatings are generally similar to the undoped silicide coatings. The growth mechanism for the five-layered Ge-doped silicide coatings is generally different from the undoped silicides. The growth of dual-layer Ti-boride coatings was also studied.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 48 (1997), S. 527-551 
    ISSN: 1573-4889
    Keywords: chloridation ; oxidation ; Fe-Cr alloys ; Ni-Cr 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 chloridation-oxidation behavior of Fe-Cr (0–25 wt. %Cr) and Ni-Cr (0–20 wt.%Cr) alloys was studied at 800°C in three different H2-HCl-H2O(ν) environments. In a low-HCI and low-H2O(ν) environment, where Cr2O3 is thermodynamically stable, the corrosion resistance of the Fe-Cr alloys increased with increasing Cr content in the alloys. In a high-HCl and high-H2O(ν) environment, where FeCr2O4 is stable and CrCl2 is metastable, the corrosion resistance of the Fe-Cr alloys depended similarly on the Cr content. Low-Cr-Fe-Cr alloys exhibited large weight losses, while Fe-Cr alloys with higher than 19 wt. %Cr showed good corrosion resistance. In an environment of high-HCl in the absence of H2O(ν), the evaporative corrosion rate was fast and limited by gas phase diffusion, and independent of the Cr content in the Fe-Cr alloys. Ni and Ni-Cr alloys generally showed good corrosion resistance in the environments of high H2O(ν) because of the low NiCl2 vapor pressure and formation of a protective Cr2O3 scale. However, in the environment of high HCl in the absence of H2O(ν), selective formation and evaporation of CrCl2 occur, which results in Cr depletion and networks of voids for even a high-Cr Ni-Cr alloy.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 48 (1997), S. 553-596 
    ISSN: 1573-4889
    Keywords: chloridation ; oxidation ; HCl ; high-temperature alloys ; high-temperature corrosion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Chloridation-oxidation studies of nine commercial high-temperature alloys were carried out at 800°C in three different H2-HCl-H2O(ν) environments: (A) both low HCl and H2O(ν) partial pressures, where either Cr2O3 or FeCr2O4 is stable, (B) both high HCl and H2O(ν) partial pressures, where FeCrO4 is stable and CrCl2 is metastable, and (C) high HCl partial pressure in the absence of H2O(ν), where either CrCl2 or Cr2O3 is stable. Although alloy 600 has the lowest Cr content of these nine alloys, it showed excellent corrosion resistance in all three environments because of its high Ni content. Alloy 304, with the lowest Ni content of the nine alloys, exhibited poor corrosion resistance in the environment C, fair resistance in the environment B and good resistance in the environment A. Alloy 800 showed very good resistance in Environment A, and fair corrosion resistance in Environment B; however, it suffered linear weight-loss kinetics when exposed to Environment C The alloys 617, 214, HR-160, X, 230 and 86 have good corrosion resistance in Environments A and B because of their relatively high contents of oxide-scale-forming elements Cr and/or Al. In Environment C, chlorine dramatically decreased the adhesion of the scale on the surface, and aluminum in alloys 617 and 214 hardly showed its usual beneficial effect in combating corrosion, nor does silicon in alloy HR-160. Different corrosion mechanisms are proposed for the alloys in the different environments.
    Type of Medium: Electronic Resource
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