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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 8 (1978), S. 145-160 
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract The corrosion behaviour of Ni in molten Na2SO4, NaCl, and in mixtures of these two salts, at 900° C, in laboratory air and under O2+SO2/SO3 atmospheres has been examined by electrochemical curves and topochemical analysis of corrosion products. Ni passivity in pure Na2SO4 was observed under potentiodynamic and potentiometric conditions, the passive film corresponding to NiO. Passivity was not so easy to achieve in chloride melts as in sulphate alone, but once a thick oxide film forms on the specimen, the Cl− addition is accompanied by an increase in the film stability. The inhibiting role of NaCl on Ni in the passive-transpassive area was also evidenced. In opposition, halide additions (especially those up to 25%) increased the dissolution current densities of Ni in the active region. These higher dissolution rates are represented by the equation Ni3S2+4NaCl+1/2 O2 = 2NiCl2+2Na2S + NiO which is also suggested as a critical factor in the Ni passivation. The passive capability found for Ni in Na2SO4/NaCl melts, in air, is destroyed by SO3 atmospheres. This corrosion-stimulation is due to the SO3 role in promoting reactions such as NiS + 3O2− = Ni2++SO3+8e which would be potential-determining at the Ni surface until Ni2+ precipitates or the conjugate oxygen cathodic reduction process takes place. Microprobe analysis also evidenced S penetration which might be the reason for the Ni embrittlement. The polarization curves for Ni in pure NaCl showed the lack of a passive region; occurrence of extensive intergranular attack was also indicated by metallographic observation. The observed dissolution must occur at the expense of the Ni interactions with the species which intervene in the reaction equilibrium between O2 and molten NaCl (O2, Cl−, Cl2 and O2−) as well as with the Na+ cations, as has been discussed elsewhere. Its self-sustaining nature is enhanced by the continuous reduction of the nickel ion content of the melt by NiCl2 evaporation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 8 (1978), S. 179-193 
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract The corrosion behaviour of Ni in molten Na2SO4, NaCl, and in mixtures of these salts at 900° C, has been studied by electrochemical and topochemical methods. Microprobe analysis showed deep S penetration which causes embrittlement of the specimens by intergranular attack.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 19 (1989), S. 467-468 
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-4889
    Keywords: preoxidation ; coal gasification ; alumina-former ; mechanical alloy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Iron-based mechanical alloys containing 3.2–6.6 Al, 16.0–24.7 Cr, 0.5 Ti, and 0.5 Y2O3 (mass%) were preoxidized in air at 1373 K for 10–180 min. Alumina scales were formed. Scales were isolated and examined in a high-voltage transmission electron microscope. Specimen sections were examined in a scanning electron microscope. Specimens were exposed to atmospheres exhibiting oxygen activities from 1.5×10−13 to 1.4×10−14 and sulfur activities from 7.4×10−7 to 3.6×10−5 at 1123, 1223, and 1323 K. Alumina, chromia, and iron sulfide are thermodynamically stable under these conditions. Sulfidation did not occur at 1223 or 1323 K. Specimens exposed at 1123 K were sulfidized and formed a scale containing iron, chromium, and sulfur. The period before the onset of sulfidation was dependent on the preoxidation time. A model is developed to account for the temperature dependence of the sulfidation in terms of the alloy-interdiffusion rate of aluminum and the activity of the sulfidizing species at the scale-gas interface.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 39 (1993), S. 371-388 
    ISSN: 1573-4889
    Keywords: superalloy ; sulphidation-oxidation ; sulphate layer corrosion mechanism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The high-temperature-corrosion behavior of a Ni-Co-Cr-Si superalloy (HAYNES Alloy HR-160) in an SO2+O2 (SO2∶O2=2∶1) has been studied at 625°C and 750°C. Alloy samples were corroded for 72 hr, followed by XRD, SEM, EDS, and XPS analysis on the surface and/or cross-section of the samples. It was found that the simultaneous nucleation of nickel and cobalt oxides and chromia at the initial stage lead to the subsequent formation of a sulphate layer on reaction with the gas phase. This eventually lead to the formation of a thick sulphide layer above the chromia scale. The stable phases for Cr, Ni, and Co in such an atmosphere are chromia as well as Ni and Co sulphates. The existence of a thin sulphate layer was suggested some time ago but could not be detected and was disputed. The XPS analysis in this work now provides evidence for the existence of this sulphate layer. The transport of sulphur through the oxide scale into the alloy substrate is discussed. It was concluded that sulphur advanced into the substrate by the oxidation of sulphides, thus liberating the sulphur. The possibility of sulphur transport in the form of SO2 molecules was also discussed. Based on the results and discussion, a schematic corrosion mechanism is presented.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 41 (1994), S. 81-101 
    ISSN: 1573-4889
    Keywords: sulfidation ; oxidation ; alloy 800H, SO2−O2 ; H2−H2S
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The high-temperature-corrosion behavior of alloy 800H has been studied in an oxidizing (SO2−O2, $$P_{O_2 }$$ =0.23 atm, $$P_{s_2 } $$ =1.9×10−29 atm) and a reducing (H2−H2S−CO−CO2−N2, $$P_{O_2 }$$ =1.5×10−18 atm $$P_{s_2 } $$ =4.3×10−8 atm, ac=0.03) sulfidizing environment, at 750°C and 850°C, respectively. When corroded in SO2−O2, the protective chromia scale which developed on the alloy in the early stages cracked and spalled in quite a short time period. This led to the growth of iron and nickel sulfides beneath the chromia layer, causing more chromia spallation. When correded in H2−H2S−CO−CO2−N2, the alloy exhibited breakaway corrosion in about 35hr, at which stage liquid nodules formed on the sample surface. The nodules were studied in detail and were found to consist of three layers. The growth mechanism of such nodules is proposed.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 20 (1985), S. 449-456 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Certain metal halide vapour complexes of the type ABX m+n increase the equilibrium vapour concentration of one or both of the component salts in the binary system (AXm/BXn). Such enhancement depends upon the free energy of complex formation, the saturated vapour pressure of the complexing salt and the melt activities, in a manner formulated here by means of a thermodynamic scheme. Certain trends in the periodic table are established.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 14 (1995), S. 858-860 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 14 (1995), S. 1089-1091 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 20 (1985), S. 457-466 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Stable vapour complexes of the type ABX m+n can sometimes increase the vapour concentration of a low volatility salt above the liquid pool. If the equilibrium concentration of A and/or B, in all their molecular forms above the binary melt AX m /BX n exceed their values above their respective pure salts enhancement (F〉1) has occurred. Mass spectrometric data suggests that such enhancement may occur in two dissimilar systems NaCl/ PbCl2 (F Na〉1) and NaCl/DyCl3 (F Dy〉1). Vapour transport and electrical discharge lamp experiments have been used to test this prediction by direct measurement of the enhancement and the results are reported here.
    Type of Medium: Electronic Resource
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