Abstract
Wagner's criterion to predict the minimum concentration of solute (N 0B(min) )necessary for the exclusive formation of its scale has been modified to incorporate both thermodynamic and kinetics requirements. The analysis presented here involves a receding alloy/scale interface for which the composition of the alloy at this interface is governed by thermodynamic equilibrium between the two competing scale phases and the base alloy. This is a more rigorous analysis than that of Wagner's, who assumed the alloy/scale interface to be immobile and the solute composition at the interface to be zero. A comparison is made between values of N 0B(min) found experimentally and those predicted by Wagner's and the present criterion for a number of alloy-gas systems. It is shown that the criterion developed in the present analysis can often provide a better approximation of the actual N 0B(min) .The expressions derived from the present analysis have been extended also in a semiquantitative manner to provide a criterion for the minimum amount of solute in the alloy required for the transition from internal to external scale formation.
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Wang, G., Gleeson, B. & Douglass, D.L. An extension of Wagner's analysis of competing scale formation. Oxid Met 35, 317–332 (1991). https://doi.org/10.1007/BF00738292
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DOI: https://doi.org/10.1007/BF00738292