Author
Listed:
- M. KONO
(Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, British Columbia, Canada V6T 1Z1, Canada)
- X. SUN
(Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, British Columbia, Canada V6T 1Z1, Canada)
- R. LI
(Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, British Columbia, Canada V6T 1Z1, Canada)
- K. C. WONG
(Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, British Columbia, Canada V6T 1Z1, Canada)
- K. A. R. MITCHELL
(Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, British Columbia, Canada V6T 1Z1, Canada)
- T. FOSTER
(Dockyard Laboratory (Pacific), Defence Research Establishment Atlantic, PO Box 17000 Stn. Forces, Victoria, British Columbia, Canada V9A 7N2, Canada)
Abstract
X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and scanning electron microscopy (SEM) have been used to characterize surfaces of aluminum which have been pretreated by mechanical polishing, acid etching and alkaline etching, as well as given subsequent exposures to air and water. These surfaces can differ markedly with regard to their chemical compositions and topographical structures. Characterizations of these surfaces after exposures to three organosilanes, γ-GPS, BTSE and γ-APS, indicate that the amount of silane adsorbed in each case shows a tendency to increase both with the number of OH groups detected at the oxidized aluminum and with the surface roughness. The XPS data are consistent with the adhesion of γ-APS occurring through H bonding, especially via NH3+groups.
Suggested Citation
M. Kono & X. Sun & R. Li & K. C. Wong & K. A. R. Mitchell & T. Foster, 2001.
"Characterization Of Aluminum Surfaces After Different Pretreatments And Exposure To Silane Coupling Agents,"
Surface Review and Letters (SRL), World Scientific Publishing Co. Pte. Ltd., vol. 8(01n02), pages 43-50.
Handle:
RePEc:wsi:srlxxx:v:08:y:2001:i:01n02:n:s0218625x01000938
DOI: 10.1142/S0218625X01000938
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