Abstract
The kinetics of tin electrodeposition during the electrolytic coloring of porous anodic oxide films on aluminum is studied as a function of the oxide properties, e.g., the thickness of the porous oxide layer, and the surface resistance offered by the barrier oxide layer. While the thickness of the porous oxide layer is controlled by the anodization time, the surface resistance is controlled by the anodization voltage, and the anodization bath temperature. Steady-state polarization measurements are employed to characterize the dependence of the coloring kinetics on the oxide properties. Measurements indicate that the kinetics of the electrolytic coloring process can be accelerated by: (i) reducing the surface resistance of the oxide film (primarily offered by the barrier oxide layer) by growing the oxide at a lower anodization voltage, and/or a higher bath temperature, or (ii) growing a thinner porous oxide layer by decreasing the anodization time. The electrochemical measurements are supported by gravimetric analysis of electrolytically colored alumina samples (using calibrated wavelength-dispersive X-ray fluorescence spectroscopy), and by optical spectrophotometry.
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Acknowledgements
We would like to thank Steve Gaarenstroom (General Motors CES Lab) for the tin loading measurements. Helpful discussions with Professor Uziel Landau are acknowledged.
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Akolkar, R., Wang, YM. & Kuo, HH. Kinetics of the electrolytic coloring process on anodized aluminum. J Appl Electrochem 37, 291–296 (2007). https://doi.org/10.1007/s10800-006-9258-0
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DOI: https://doi.org/10.1007/s10800-006-9258-0