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  • 1
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemistry of materials 4 (1992), S. 245-247 
    ISSN: 1520-5002
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemistry of materials 7 (1995), S. 1807-1815 
    ISSN: 1520-5002
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 27 (1994), S. 11-25 
    ISSN: 1572-879X
    Keywords: cuprous sulfide ; resistance relaxation ; reaction pathways ; non-stoichiometry ; rate limiting step ; sulfur activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The kinetics of sulfur transfer from H2S to cuprous sulfide (digenite) at 500°C has been established by the resistance relaxation technique. The resistance measurements have been carried out by the van der Pauw method, which uses a four probe configuration. The rate of the forward reaction decreases with the increase in the activity of sulfur in the sulfide (rate ∞a s −0.55 ) while the rate of the backward reaction is found to be nearly independent of the sulfur activity. Based on these results, the rate limiting step for sulfur transfer reaction to digenite is shown to be: H2S (g) + 2e− = S2−(ad) + H2(g).
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 22 (1984), S. 133-146 
    ISSN: 1573-4889
    Keywords: growth stresses ; grain boundary transport ; elastic analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A quantitative analysis of oxide growth stresses is carried out for the model advanced by Rhines and Wolf in which new oxide forms along preexisting oxide grain boundaries. The mean oxide stress developed within the oxide is calculated using standard techniques from continuum dislocation theory. This analysis shows that the mean growth stress is compressive and is directed parallel to the oxide/ matrix interface. The growth stress is found to be independent of the oxide scale thickness, provided that the scale is thicker than the oxide grain size. However, in thin scales, the growth stress is very sensitive to oxide scale thickness. The compressive growth stress increases in direct proportion to the width of the new grain boundary oxide layer formed. The oxide scale is expected to either fail by buckling, or the growth mode will change to one in which additional compressive stresses are not generated.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 22 (1984), S. 247-275 
    ISSN: 1573-4889
    Keywords: corrosion product ; thermochemical analysis
    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 of metallic components is a significant problem in many high temperature processes. In studying such corrosion phenomena, the scientist must identify simpler laboratory environments which can reproduce the corrosion product composition and morphology found in the more complex service environments. The present work was undertaken to develop a graphical method to aid in accomplishing the above objective. A predominantly oxidizing-sulfidizing environment which also contains some carbon was selected as an example. Such an environment is characteristic of processes such as coal gasification and can be produced by mixing CO2, H2, and H2S in appropriate quantities. Starting from selected initial compositions of such gas mixtures, an approach based upon free energy minimization was used to determine which condensed corrosion product phases will be stable for selected metals, temperatures, and total pressure. Graphs with initial CO2/H2 and H2S/H2 ratios as axes were then constructed; in these graphs, areas represent single condensed phases, lines represent two condensed phases in equilibrium, and triple points represent three condensed phases in equilibrium. The graph indicates at a glance the product phases which are possible for a given initial gas composition. When dealing with alloys, diagrams for the component pure metals must be combined.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 24 (1985), S. 17-27 
    ISSN: 1573-4889
    Keywords: nucleation ; diffusion ; supersaturation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The present study reports on the in situ oxidation of copper to Cu2O and subsequent reduction to metallic copper in an environmental scanning electron microscope. The oxidation was carried out at approximately 125 μm oxygen pressure while the reduction was done at the same pressure using H2 gas. The first visible signs of oxidation occurred in about 2 min: submicron size nuclei of Cu2O formed randomly on the metal surface. No preferred nucleation along grain boundaries could be observed. The surface was completely covered with Cu2O in about 30 min of oxidation time, the final average grain size of Cu2O being approximately 3 μm. The reduction kinetics of Cu2O were slower than the oxidation kinetics, the first visible copper nuclei appearing only after about 6 min of reduction. A reduction mechanism is suggested where the diffusion of copper vacancies from the copper particle-Cu2O interface to the Cu2O-H2 interface limits the overall kinetics. Based on this assumption, a copper supersaturation corresponding to a copper activity of 1.0005 in Cu2O has been calculated.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 40 (1993), S. 179-196 
    ISSN: 1573-4889
    Keywords: computational modeling ; carburization ; denuded-zone ; diffusion-dissolution ; finite difference method ; Newton-Raphson methodology ; defect chemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Heat-resistant alloys used in mixed-oxidant environments rely on the formation of a chromia, alumina, or silica surface film for corrosion resistance and the presence of second-phase precipitates in the matrix often for their strength properties. The growth of the oxide film on such alloys is often accompanied by the dissolution of precipitates in the alloy subsurface region. Continued oxidation combined with oxide-scale spallation tends to decrease the content of the oxide-forming constituent to such a level that protective scaling can no longer occur and severe degradation can develop. In the present work, the initial corrosion processes involving the complex coupling between oxide scale growth and precipitate dissolution is simulated computationally. As an example, a Ni-Cr alloy containing Cr 23 C 6 precipitates was exposed to an oxidizing-carburizing environment. An approach combining finite difference and Newton-Raphson methodologies is developed to model this diffusion/ dissolution process, incorporating the point-defect-chemistry aspects of the oxide scale. The model is able to predict the chemical and microstructural evolution of high-chromium austenitic alloys during the initial stages of oxidation-carburization.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 22 (1984), S. 83-100 
    ISSN: 1573-4889
    Keywords: alumina scales ; doping ; adherence ; plasticity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract In the present study, the effect of adding yttrium to alloys is investigated. The microstructure of the cast Fe-25Cr-4Al-0.5Y alloy used in the study shows that the vttrium is present in different shapes and sizes as the intermetallic phase, (Fe, Cr)4(Al, Y), previously unreported in the literature. Upon oxidation in dry oxygen in the 1100–1200 °C temperature range, a columnar, fine-grained (0.5–1 μm) α-Al2O3 scale is formed which grows predominantly by inward oxygen grain-boundary transport. The intermetallic phase, during incorporation into the oxide scale, is converted into Y3Al5O12, the chromium and iron from the intermetallic diffusing back into the metal matrix. The Y3Al5O12 phase saturates the oxide scale with yttrium, which segregates to oxide grain boundaries. The microstructural features of the oxide scale resemble those of the scale formed on the yttria-dispersed alloy we investigated earlier. The improved adherence of the oxide scale is a consequence of yttrium doping, which facilitates the formation of a fine-grained scale in which oxide growth stresses can be relieved by diffusional plastic flow. Further, yttrium suppresses Al transport in the oxide scale and prevents Al2O3 nucleation within the scale, a process which can generate compressive stresses in the scale. The yttrium doping in the oxide scale is somewhat more efficient when it is present as a dispersoid in the metal.
    Type of Medium: Electronic Resource
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