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Delamination of Poylmer Coatings from Metal Substrates: Submicroscopic and Molecular Aspects

Published online by Cambridge University Press:  11 February 2011

M. Rohwerder
Affiliation:
Max-Planck-Institut für Eisenforschung, Max-Planck-Str.1, D-40237 Düsseldorf, Germany
E. Hornung
Affiliation:
Max-Planck-Institut für Eisenforschung, Max-Planck-Str.1, D-40237 Düsseldorf, Germany
Xing-Wen Yu
Affiliation:
Max-Planck-Institut für Eisenforschung, Max-Planck-Str.1, D-40237 Düsseldorf, Germany
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Abstract

Delamination of organic coatings from metal surfaces can occur in a number of different ways, e.g. as pure cathodic delamination, as Filiform corrosion or a mixture of these. In fact, in most technical systems the pure cases are the exception and, of course, delamination is usually very slow. It has been shown that in fast delaminating systems the length scales may range between several 100 μm and several millimetres, while in systems which show slow delamination the reaction zones can be confined to submicroscopic distances [1]. This underlines the importance of investigation methods with submicroscopic resolution. As a very promising new technique Scanning Kelvin Probe Force Microscopy (SKPFM) was applied for the investigation of cathodic delamination and filiform corrosion on a submicroscopic scale [1, 2]. Indeed, these first investigations have shown that SKPFM gives basically the same information as the standard Scanning Kelvin Probe (SKP), but with a much improved resolution. It could be shown, for instance, that the extension of the reaction zone seems to be much narrower than would have to be assumed from the SKP measurements. Based on the knowledge about the different delamination types that was obtained from investigations with the standard SKP [3–12] the SKPFM should be the ideal tool to get information on the submicroscopic scale. However, SKPFM alone is not sufficient for revealing the underlying fundamental mechanisms; of even higher importance is the knowledge of the molecular and mesoscopic structure at the buried interface. In this paper a design for suitable model samples is proposed and first results are presented.

Type
Research Article
Copyright
Copyright © Materials Research Society 2003

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References

REFERENCES

1. Rohwerder, M., Hornung, E. and Stratmann, M., Electrochimica Acta, in printGoogle Scholar
2. Hornung, E., Rohwerder, M., Stratmann, M., GDCh Monographies vol. 21, 22 (2000).Google Scholar
3. Leng, A., Streckel, H. and Stratmann, M., Corros. Sci. 41, 547 (1999).Google Scholar
4. Leng, A., Streckel, H. and Stratmann, M., Corros. Sci. 41, 579 (1999).Google Scholar
5. Leng, A., Streckel, H., Hofmann, K. and Stratmann, M., Corros. Sci. 41, 599 (1999).CrossRefGoogle Scholar
6. Fürbeth, W. and Stratmann, M., Corrosion Science 43, 207 (2001).CrossRefGoogle Scholar
7. Fürbeth, W. and Stratmann, M., Corrosion Science 43, 229 (2001).Google Scholar
8. Fürbeth, W. and Stratmann, M., Corrosion Science 43, 243 (2001).Google Scholar
9. Rohwerder, M. and Stratmann, M., MRS Bulletin 24, 43 (1999).CrossRefGoogle Scholar
10. Schmidt, W. and Stratmann, M., Corros. Sci. 40, 1441 (1998).CrossRefGoogle Scholar
11. de Wit, J.H.W., Electrochimica Acta 46, 3641 (2001).Google Scholar
12. Williams, G., McMurray, H. N., Hayman, D. and Morgan, P. C., PHYSCHEMCOMM 6, 1 (2001).Google Scholar
13. Rohwerder, M., de Weldige, K. and Stratmann, M., J. of Solid State Electrochemistry 2, 88 (1998).Google Scholar
14. Vago, E.R., de Weldige, K., Rohwerder, M., Stratmann, M., Fres. J. Anal. Chem 353, 316 (1995)Google Scholar