Simultaneous sulfidation-oxidation of nickel at 603°c in argon-so2 atmospheres |
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Authors: | K L Luthra W L Worrell |
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Affiliation: | (1) Corporate Research and Development, General Electric Co., 12301 Schenectady, NY;(2) University of Pennsylvania, 19104 Philadelphia, PA |
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Abstract: | The simultaneous oxidation-sulfidation rate of nickel has been measured as a function of SO2 pressure (0.04 to 1 atm) in Ar-SO2 gas mixtures at 603°C. The observed corrosion rates are about 107 times faster than the oxidation rate of nickel in oxygen at 1 atm. The product scale consists of an inner Ni3S2 layer and an outer two-phase layer of NiO and Ni3S2. A linear rate law is observed during an initial time period, and the most probable rate-controlling step is dissociation
of SO2. An increase in the scale-gas interfacial area increases the corrosion rate during intermediate time periods. With increasing
time, parabolic corrosion rates are measured for SO2 pressures of 0.25 and 1 atm. Values of the nickel diffusivity in Ni3S2 calculated from our measured parabolic-rate constants are in good agreement with recently reported values. This agreement
indicates that an interconnected Ni3S2 phase in the outer two-phase layer provides rapid transport paths for nickel diffusion through the scale.
Formerly a Graduate Student in the Department of Metallurgy and Materials Science at the University of Pennsylvania, Philadelphia,
PA |
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