Abstract
Effects of hydrodynamic conditions, current density and solution temperature on the d.c. electrodeposition of Fe−Ni−Co alloys have been investigated with stationary planar and rotating cylindrical electrodes. The deposition rate of Fe showed mass transfer effects at cathodic potentials ≤−1.35 V/sce. Deposition of Ni appeared to be kinetically controlled; deposition of Co appeared to be under kinetic control at potentials ≥−1.35 V/sce but under mixed control at −1.65 V. Current efficiency of the codeposition process increased with increasing current density and decreased with increasing rotation rate. Higher solution temperatures and rotation rates extended the applied current density range where smooth, adherent, and metallic-looking deposits could be obtained. An increase in solution temperatures also decreased anomalous codeposition of Fe−Ni−Co. Calculations based on the Hessami-Tobias model provide qualitative agreement with dependence of experimental electrodeposition on applied current density, hydrodynamics and temperature.
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Phan, N.H., Schwartz, M. & Nobe, K. Electrodeposition of Fe−Ni−Co alloys part I: Direct current deposition. J Appl Electrochem 21, 672–677 (1991). https://doi.org/10.1007/BF01034044
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DOI: https://doi.org/10.1007/BF01034044