Formation of ultra-thin amorphous conversion films on zinc alloy coatings Part 1. Composition and reactivity of native oxides on ZnAl (0.05%) coatings

被引:42
作者
Fink, N [1 ]
Wilson, B [1 ]
Grundmeier, G [1 ]
机构
[1] Max Planck Inst Eisenforsch GmbH, Christian Doppler Lab Polymer Met Interfaces, D-40237 Dusseldorf, Germany
关键词
FT-IRRAS; AFM; XPS; alkaline cleaning; galvanised steel;
D O I
10.1016/j.electacta.2005.08.030
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Within the two parts of this contribution a detailed investigation of the nucleation and growth of ultra-thin amorphous conversion coatings on hot dip galvanised steel is reported. The first part deals with the composition and reactivity of the native ultra-thin oxyhydroxide films that are formed on the zinc alloy surface during the hot dip galvanising process due to the enrichment of aluminium at the outer surface of the alloy coating. Complimentary surface analytical techniques such as FT-IR-spectroscopy at grazing incidence and X-ray photo electron spectroscopy, high resolution AFM on selected grains to study the surface topography and cyclovoltammetry as well as quasi stationary current potential curves and Kelvin probe measurements to study surface ion and electron transfer reactions were applied. Changes in the chemical composition, the electronic properties and the morphology of the ultra-thin surface could thereby be analysed. The surface of the ZnAl alloy is composed of an about 3-4 nm thick mixed Zn and Al-oxyhydroxide layer with Zn-oxyhydroxide slightly enriched at the outermost surface. This mixed oxyhydroxide causes to a significant inhibition of electron transfer reactions. During alkaline cleaning the surface is nanoscopically roughened and the mixed oxyhydroxide is converted into an electro-conducting hydroxyl rich pure Zn-oxyhydroxide layer with a thickness of about 4 nm. In the second part of this paper the effect of the inorganic surface layer on the film formation is correlated with these findings. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2956 / 2963
页数:8
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