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Electrochemical impedance study of platinum electrode in fused Na[sub 2]SO[sub 4]-10 mole percent NaVO[sub 3] melts

Journal Article · · Journal of the Electrochemical Society; (United States)
DOI:https://doi.org/10.1149/1.2043853· OSTI ID:6537538
;  [1]
  1. Ohio State Univ., Columbus, OH (United States). Dept. of Materials Science and Engineering
Sodium sulfate, the most common salt deposit involved in hot corrosion, results from the combustion of S-containing fuel in an NaCl-containing air. Another particularly harmful species in hot corrosion is vanadium, which may originate from low-grade V-containing fuels. During combustion of the low-grade fuel, Na[sub 2]SO[sub 4], V[sub 2]O[sub 5], and NaVO[sub 3] form as condensed phases which cause hot corrosion of the combustion equipment. An electrochemical impedance study was made for a platinum working electrode in Na[sub 2]SO[sub 4]-10 mole percent (m/o) NaVO[sub 3] melts in a temperature range of 1,150 to 1,200 K. The principal electroactive oxidant is a solute of V[sub 2]O[sub 5], which has a lower Warburg coefficient than that for the major oxidant S[sub 2]O[sub 7][sup 2[minus]] in pure Na[sub 2]SO[sub 4] melts in contact with 0.1 and 1%SO[sub 2]-O[sub 2] environments. The effects of temperature, basicity, oxygen potential, and polarization potential on the impedance of the system were investigated. The results are used to interpret hot corrosion induced by Na[sub 2]SO[sub 4]-NaVO[sub 3] deposits. In the vanadate-sulfate melt, the oxidant arrives at the electrode/electrolyte interface by the counterdiffusion of solutes with V[sup 4+] (V[sub 2]O[sub 4]-derived) and V[sup 5+] (V[sub 2]O[sub 5]-derived). Electron hopping in this solution does not occur.
OSTI ID:
6537538
Journal Information:
Journal of the Electrochemical Society; (United States), Journal Name: Journal of the Electrochemical Society; (United States) Vol. 142:1; ISSN JESOAN; ISSN 0013-4651
Country of Publication:
United States
Language:
English