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  • oxidation  (24)
  • Springer  (24)
  • Annual Reviews
  • 1980-1984  (10)
  • 1975-1979  (14)
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  • Springer  (24)
  • Annual Reviews
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  • 1
    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′.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 13 (1979), S. 437-456 
    ISSN: 1573-4889
    Keywords: Fe-Cr ; oxidation ; kinetics ; oxide morphology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Ferritic polycrystalline Fe-24 wt.% Cr was oxidized in pure oxygen at 190 ≤ T≤490° C and pressures in the range 5.3×10−2–13.3 Pa for periods of up to 5 hr. The reaction proceeded in three stages. An initial period of accelerating rate was accompanied by oxide island nucleation and growth. Following island coalescence the rate was approximately logarithmic at low temperatures and somewhat slower than parabolic at high temperatures. Rate control during this period was thought to be due to mass transport through the oxide grain boundaries left by the island impingement process. During these first two stages the oxide formed was γ-M2O3 with possibly some spinel. The final stage of reaction involved the appearance of α-M2O3 on the outer oxide surface and a substantial slowing of the oxidation rate due to the low diffusivity in this phase.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 12 (1978), S. 247-256 
    ISSN: 1573-4889
    Keywords: oxidation ; iron ; magnetite ; oxide thickness ; electron back-scattering Mössbauer spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Magnetite films in the range 265–4520 Å have been grown on natural iron substrates and subsequently investigated by electron back-scattering Mössbauer spectroscopy. In particular, the percentage, P, of the total spectrum area contributed by the oxide has been determined as a function of oxide thickness, d. It was found that d up to ≈ 3000Å may be expressed (to an accuracy of ∼ 5%) by d (Å)=−1.95 × 103 ln (1–0.01 P). The experimental data have been compared with the theoretical predictions of both Huffman and Bainbridge. Good agreement between experiment and Huffman's predictions of P is obtained using values of the electron attenuation coefficient, μ, of 1.10 × 104 cm2 g−1 for the 7.3 keV electrons and 1.73 × 104 cm2 g−1 for the 5.4 keV electrons. A good fit of our data to Bainbridge's expression requires a somewhat lower effective μ, value of 0.8 × 104 cm2 g−1. The experimental P value for the thickest oxide (4520 Å) is lower than the theoretical predictions, probably as a result of a neglected mechanism recently identified by Tricker, Ash, and Cranshaw.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 14 (1980), S. 263-277 
    ISSN: 1573-4889
    Keywords: oxidation ; Ni-Cr 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 Oxidation of the relatively simple, two-phase alloy Ni-70 wt.%Cr in oxygen between 1073 and 1473°K results in the formation of a Cr2O3 scale containing less than O.5 wt.% Ni in solid solution. The oxidation kinetics are irreproducible for an initial period, which is brief at 1073 and 1273°K but much more pronounced at 1473°K, both in duration and degree. This behavior is associated with the failure of the protective Cr2O3 scale. However, after longer periods a compact layer of Cr2O3 becomes established under isothermal conditions and results in a change to more reproducible kinetics, especially at 1073 and 1273°K. Oxidation causes chromium depletion and the formation of a single-phase zone which separates the scale and the two-phase bulk alloy. The depth of Cr2O3 internal oxide coincides with this zone. The oxidation behavior is compared with that of more Ni-rich, single-phase Ni-Cr alloys, with particular reference to the effects of the constitution of the underlying alloy and the integrity of the protective oxide.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 18 (1982), S. 295-314 
    ISSN: 1573-4889
    Keywords: Nickel-manganese alloys ; oxidation ; solid solution scales ; internal oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Ni-Mn alloys containing up to 38% Mn have been oxidized in pure oxygen between 873 and 1273 K and the parabolic rate constants measured. The scale morphologies and oxide compositions are interpreted in terms of modifications to the scale on pure Mn caused by the presence of Ni. The scales are composed predominantly of two layers at all temperatures, giving the sequences of phases alloy/cubic monoxide (Ni, Mn)O/ternary spinel, with the cubic (Ni, Mn)O layer always having the greater thickness. There is limited evidence for a third, very thin, outer layer in the scales on all alloys at 873 K and for Ni-38%Mn at 1073 K, which is tentatively considered to be Mn2O3, giving layers in the order alloy/cubic monoxide/ternary spinel/Mn2O3, by analogy with the scale formed on pure Mn. The distribution of the alloy components in the scale is discussed in relation to the Ni-Mn-O phase diagram and in terms of recent theoretical treatments of solid solution scale formation on binary alloys, as far as the available diffusion data allow. The occurrence of internal and intergranular oxidation and the formation of a Mn-depleted zone coincident with the band of uniform internal oxide are considered briefly.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 23 (1982), S. 147-150 
    ISSN: 1432-1041
    Keywords: methaqualone ; debrisoquine ; pharmacogenetics ; metabolism ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The metabolism of methaqualone to the glucuronides of 5 C-monohydroxy metabolites and to the N-oxide has been studied in 2 groups of healthy young adults phenotyped as extensive and poor metabolisers of debrisoquine. No significant interphenotype differences were observed with respect to the excretion of any of the 6 metabolites. It is probable that the genetic regulation of the pathways leading to these metabolites is at a locus other than that which is responsible for the regulation of the oxidation of debrisoquine, guanoxan, phenacetin, phenytoin and sparteine.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 16 (1981), S. 339-353 
    ISSN: 1573-4889
    Keywords: Iron-carbon ; oxidation ; decarburization
    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 Fe-C alloys in the temperature range 600–850°C has been studied. CO 2 evolved during oxidation was measured using an infrared gas analyzer. The presence of C lowers the oxidation rate relative to that of pure Fe and this has been related to the rejection of carbon at the alloy-scale interface causing poor contact between scale and alloy. As a result, the scale contains a higher proportion of magnetite, which reduces its overall growth rate. Very little carbon is lost to the atmosphere. The ease with which the rejected carbon is incorporated into the alloy depends on the alloy structure.
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  • 8
    ISSN: 1573-4889
    Keywords: oxidation ; hot corrosion ; ESCA ; superalloys ; sodium sulfate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A study of the high-temperature oxidation and Na2SO4-induced hot corrosion of some nickel-base superalloys has been accomplished by using ESCA to determine the surface composition of the oxidized or corroded samples. Oxidation was carried out at 900 or 1000°C in slowly flowing O2 for samples of B-1900, NASA-TRW VIA, 713C, and IN-738. Oxidation times ranged from 0.5 to 100 hr. Hot corrosion of B-1900 was induced by applying a coating of Na2SO2 to preoxidized samples, then heating to 900° C in slowly flowing O2. Corrosion times ranged from 5 min to 29 hr. For oxidized samples, the predominant type of scale formed by each superalloy was readily determined, and a marked surface enrichment of Ti was found in each case. For corroded samples, the transfer of significant amounts of material from the oxide layer to the surface of the salt layer was observed to occur long before the onset of rapidly accelerating weight gain. Some marked changes in surface composition were observed to coincide with the beginning of accelerating corrosion, the most striking of which were a tenfold decrease in the sulfur to sodium ratio and an increase in the Cr(VI) to Cr(III) ratio.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 14 (1980), S. 517-530 
    ISSN: 1573-4889
    Keywords: CoCrAl ; oxidation ; oxide-scale adherence ; platinum ; rare-earth effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The effects of small Pt additions (1 or 3 wt.%) on the oxidation behavior of Co-10Cr-11Al and a similar alloy containing Hf have been studied. An intermetallic phase was present in the alloy containing Hf and Pt but not in that containing Pt alone. The size and distribution of the intermetallic was comparable to that of similar alloys containing oxide dispersions produced by a controlled internal oxidation treatment. As a consequence it promoted the formation of inwardly growing Al2O3 pegs that helped key the surface scale to the substrate and improve the scale-metal adhesion in both isothermal and cyclic oxidation tests. The improvement in overall oxidation resistance relative to an addition-free alloy was considerable, and similar to that of the best oxide dispersion-containing alloys.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 9 (1975), S. 409-413 
    ISSN: 1573-4889
    Keywords: cobalt ; cobalt-chromium alloys ; silicon ; oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Some investigators have reported that Co-25 wt.% Cr oxidizes slowly at temperatures in the range 1000–1200°C forming a protective Cr2O3 scale; and this is the normal behavior of cobalt-base superalloys. Others have reported very rapid oxidation, forming a two-layer scale: an outer CoO layer and an inner mixture of Cr2O3 and CoCr2O4 particles in a CoO matrix. This investigation shows that the principal reason for this behavior is the purity of the material; it appears that the rapid mode of oxidation is the intrinsic behavior for high purity material. The most probable impurity to produce the slower mode is silicon, and it is shown that as little as 0.05 wt. % Si is sufficient to change the mode of oxidation provided sufficient oxygen is also present in the alloy: it seems probable therefore that a fine dispersion of SiO2 is responsible.
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