Relation between microstructural aspects of AA2024 and its corrosion behaviour investigated using AFM scanning potential technique

Citation
P. Campestrini et al., Relation between microstructural aspects of AA2024 and its corrosion behaviour investigated using AFM scanning potential technique, CORROS SCI, 42(11), 2000, pp. 1853-1861
Citations number
12
Categorie Soggetti
Material Science & Engineering
Journal title
CORROSION SCIENCE
ISSN journal
0010938X → ACNP
Volume
42
Issue
11
Year of publication
2000
Pages
1853 - 1861
Database
ISI
SICI code
0010-938X(200011)42:11<1853:RBMAOA>2.0.ZU;2-F
Abstract
The microstructure of the aluminium alloys has a large influence on the cor rosion behaviour. In particular, the intermetallic particles play an import ant role in the corrosion resistance of aluminium alloys and they can give rise to localized corrosion, such as pitting and exfoliation, because of th e formation of galvanic cells. The shape, size and chemical composition of the intermetallic particles are determined by the processing route (heat tr eatment and forming) carried out on the aluminium alloy. In recent work in our lab, it was found [9] that when the 2024 aluminium alloy undergoes a lo ng quench delay time (time spent in air after the homogenisation treatment) shell-shaped particles precipitate. These are characterized by differences in chemical composition between the core and the surface. Simultaneously, the corrosion mechanism of the AA2024 changes from general to localized. Th erefore, it was thought that the shell-shaped particles increase the pittin g susceptibility of the 2024 aluminium alloy. In the present work, the surf ace potential of these particles was measured by means of atomic force micr oscopy (AFM) scanning potential technique. The shell-shaped particles show a large difference in potential between the core and the shell, which resul ts in a highly localized galvanic coupling. Therefore, the formation of she ll-shaped particles largely lowers the resistance to pitting attack of the AA2024. (C) 2000 Elsevier Science Ltd. All rights reserved.