Journal of Materials Science

, Volume 41, Issue 10, pp 2869–2875 | Cite as

Texture and morphology of pulse plated zinc electrodeposits

Article

Abstract

Zinc coatings were deposited under pulse-current plating conditions from an acidic sulphate bath on low-carbon steel cathodes. The effect of the (peak) deposition current density, duty cycle and pulse frequency on the microstructural texture and morphology of the deposits was studied by X-ray diffractometry and scanning electron microscopy. The zinc films consisted of crystallites having an average size controlled by deposition current density, and oriented mostly with basal (00.2) and high index (10.3), (10.4), (10.5) pyramidal planes parallel to the surface. Pulse plating resulted in coatings which were microstructurally different to those prepared under similar conditions by direct current deposition. Texture and grain size modification is illustrated. The effect of pulse current is explained in terms of enhanced nucleation and inhibited growth.

Keywords

Zinc Duty Cycle Pulse Current Pulse Frequency Zinc Coating 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    J. H. LINDSAY, R. F. PALUCH, H. D. NINE, V. R. MILLER and T. J. O’ KEEFE, Plat. Surf. Finish. 76 (1989) 62.Google Scholar
  2. 2.
    I. ZOUARI and F. LAPICQUE, Electrochim. Acta. 37 (1992) 439.CrossRefGoogle Scholar
  3. 3.
    R. WINAND, “Electrocrystallization” in “Application of Polarization Measurements in the Control of Metal Deposition” edited by I. H. Warren (Elsevier, Amsterdam, 1984) 54.Google Scholar
  4. 4.
    D. VASILAKOPOULOS, M. BOUROUSHIAN and N. SPYRELLIS, Trans. IMF. 79 (2001) 107.Google Scholar
  5. 5.
    L. PH. BÉRUBÉ and G. L'ESPÉRANCE, J. Electrochem. Soc. 136 (1989) 2314.Google Scholar
  6. 6.
    XINGPU YE, J. P. CELIS, M. DE BONTE and J. R. ROOS, ibid. 141 (1994) 2698.Google Scholar
  7. 7.
    R. WINAND, Electrochim. Acta. 39 (1994) 1091.CrossRefGoogle Scholar
  8. 8.
    V. VELINOV, E. BEŁTOWSKA-LEHMAN and A. RIESENKAMPF, Surf. Coat. Technol. 29 (1986) 77.CrossRefGoogle Scholar
  9. 9.
    M. Y. ABYANEH, J. Electroanal. Chem. 530 (2002) 82.CrossRefGoogle Scholar
  10. 10.
    N. IBL, J. CL. PUIPPE and H. ANGERER, Surf. Technol. 6 (1978) 287.CrossRefGoogle Scholar
  11. 11.
    J. CL. PUIPPE and N. IBL, Plat. Surf. Finish. 67 (1980) 68.Google Scholar
  12. 12.
    H. H. WAN and H. Y. CHEH, J. Electrochem. Soc. 135 (1988) 643.Google Scholar
  13. 13.
    D. K. KIM and H. LEIDHEISER, Metall. Trans. 9B (1978) 581.Google Scholar
  14. 14.
    H. PARK and J. A. SZPUNAR, Cor. Sci. 40 (1998) 525.CrossRefGoogle Scholar
  15. 15.
    Y. B. YIM, W. S. HWANG and S. K. HWANG, J. Electrochem. Soc. 142 (1995) 2604.Google Scholar
  16. 16.
    B. E. WARREN, “X-Ray Diffraction” (Dover Publications, New York, 1990 — corrected republication of Addison-Wesley, 1969) 253 ff.Google Scholar
  17. 17.
    I. TOMOV, CHR. CVETKOVA, V. VELINOV, A. RIESENKAMPF and B. PAWLIK, J. Appl. Electrochem. 19 (1989) 377.CrossRefGoogle Scholar
  18. 18.
    KH. SABER, C. C. KOCH and P. S. FEDKIW, Mater. Sci. Eng. A341 (2003) 174.Google Scholar

Copyright information

© Springer Science + Business Media, Inc. 2006

Authors and Affiliations

  • D. Vasilakopoulos
    • 1
  • M. Bouroushian
    • 1
  • N. Spyrellis
    • 1
  1. 1.Laboratory of General Chemistry, School of Chemical EngineeringNational Technical University of AthensZografosGreece

Personalised recommendations