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  • Articles  (8)
  • sulfidation  (8)
  • 2015-2019
  • 1990-1994  (8)
  • 1945-1949
  • 1992  (8)
  • 1947
  • Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics  (8)
  • Economics
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  • Articles  (8)
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  • 2015-2019
  • 1990-1994  (8)
  • 1945-1949
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  • Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics  (8)
  • Economics
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 37 (1992), S. 167-187 
    ISSN: 1573-4889
    Keywords: H2-H2S-H2O ; sulfidation ; NbO2 ; oxidation ; CoNb3S6
    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 Co-Nb alloys containing up to 30 wt.% Nb in H2-H2S-H2O gas mixtures was studied over the temperature range of 600–800°C. The gas composition falls in the stability region of cobalt sulfide and Nb2O5 in the phase diagrams of the Co-O-S and Nb-O-S systems at all temperatures studied. Duplex scales, consisting of an outer layer of cobalt sulfide and a complex, heterophasic inner layer, were formed at all temperatures studied. In addition to cobalt sulfide and CoNb3S6, a small amount of NbO2 was found in the inner layer. The reason for the formation of NbO2 over that of Nb2O5 in the scale is that the outer sulfide scale lowers the oxygen activity within the scale into the NbO2-stability region. Two-stage kinetics were observed for all alloys, including an initial irregular stage usually followed by a steady-state parabolic stage. The steady-state parabolic rate constants decreased with increasing amounts of Nb, except for Co-20Nb corroded at 700°C. Nearly identical kinetics were observed for Co-20Nb corroded at 600°C and 700°C. The presence of NbO2 particles leads only to a limited decrease of the available cross-section area for the outward-diffusing metal ions. The activation energies for all alloys are similar and are in agreement with those obtained in a study of the sulfidation of the same alloys. The primary corrosion mechanism involves an outward Co transport.
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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.
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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 37 (1992), S. 389-411 
    ISSN: 1573-4889
    Keywords: sulfidation ; Fe-Mo alloys ; bilayered scales ; FeMo2S4 ; Chevrel phase
    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 Fe-Mo alloys containing up to 40 wt.% Mo was studied over the temperature range 600–980
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  • 5
    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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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 37 (1992), S. 189-215 
    ISSN: 1573-4889
    Keywords: sulfidation ; Fe-Nb alloys ; FexNbS2 ; corrosion kinetics
    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 Fe-Nb alloys containing up to 40 wt.% Nb has been studied over the temperature range 600–980°C in a mixed gas of constant composition having sulfur and oxygen pressures ranging from 10−8 to 10−4 atm. and from 10−27 to 10−18 atm., respectively. All alloys were two-phase, consisting of an Fe-rich solid solution and an intermetallic compound, Fe2Nb. The scales formed on the Fe-Nb alloys were duplex, consisting of an outer layer of iron sulfide (FeS) and an inner complex layer of FexNbS2(FeNb2S4 or FeNb3S6), FeS and unreacted Fe2Nb. No oxides were detected at any temperature. The addition of Nb reduced the corrosion rate. The corrosion kinetics of Fe-Nb alloys followed the parabolic rate law, regardless of alloy composition and temperature. Platinum markers, attached to the original alloy surfaces, were always located at the interface between the inner and outer scales.
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  • 7
    ISSN: 1573-4889
    Keywords: sulfidation ; Fe-Cr-Al alloys ; kinetics ; structures ; sulfide compositions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Sulfidation of an Fe-23.4Cr-18.6Al (at.%) alloy was investigated in H2S-H2 atmospheres, $$10^{ - 6} \leqslant {\text{P}}_{{\text{S}}_{\text{2}} } \leqslant 10^2 $$ Pa, at 973 K. It was found over this pressure range that sulfidation after an early transient period followed the parabolic rate law, being diffusion controlled. An investigation was carried out of the scales formed during early transient sulfidation over the sulfur pressure range $${\text{p}}_{{\text{S}}_{\text{2}} } = 10^{ - 6} - 10^{ - 2} $$ Pa. Fully developed scales were multilayered consisting of an inner compact layer of equiaxed grains, an intermediate layer of equiaxed and columnar grains exhibiting a small degree of porosity, and an outer porous layer of distinct plates and needles. The grains of the inner and intermediate layers contained quarternary sulfide phases. The following phases were identified: spinels (CrFe)Al2S4 and (FeAl)Cr2S4, hexagonal (FeCr)Al2S4, (CrAlFe)2S3, and (CrAlFe)5S6. The plates and needles were composed of hexagonal (FeCr)Al2S4 and (CrAlFe)2S3 at $${\text{p}}_{{\text{S}}_{\text{2}} } \geqslant 10^{ - 6} $$ and 10−5 Pa from which pyrrhotite, FeS, grew at $${\text{p}}_{{\text{S}}_{\text{2}} } \geqslant 10^{ - 4} $$ .
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 38 (1992), S. 465-482 
    ISSN: 1573-4889
    Keywords: niobium ; sulfidation ; defect structure ; hydrogen doping
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract An approximate model for the defect structure of the niobium sulfide 2s Nb1+xS2 is developed on the basis of experimental data concerning its deviation from stoichiometry as a function of sulfur pressure. The model involves the presence of doubly-charged metal interstitials and metal vacancies as well as of free electrons and electron holes. The possible effects of hydrogen dissolution on the concentration of the intrinsic defects in this compound are also evaluated for various hydrogen species with an effective charge different from zero, but no final conclusion concerning the existence of an actual doping effect of this compound is reached. The rate constant for the sulfidation of niobium at 950°C is calculated on the basis of this defect structure as a function of the sulfur pressure and is compared with the experimental results concerning the sulfidation of niobium in H2-H2S mixtures. It is concluded that both metal vacancies and metal interstitials contribute significantly to the growth of the sulfide 2s Nb1+xS2
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