Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Revisiting zinc passivation in alkaline solutions

Loading...
Thumbnail Image

Authors

Thomas, S.
Cole, I. S.
Sridhar, M.
Birbilis, N.

Journal Title

Journal ISSN

Volume Title

Publisher

Access Statement

Research Projects

Organizational Units

Journal Issue

Abstract

Passive films nominally consist of an inner compact oxide and the outer precipitated layer. In the case of zinc (Zn), the outer layer is mainly precipitated ZnO/Zn(OH)2. Electrolyte pH controls the stability of the outer precipitated layer. In a pH 13 solution, formation of soluble Zn(OH)3- and Zn(OH)42- phases render the precipitated layer unstable increasing zinc corrosion, whereas at pH 12, the precipitated layer (ZnO/Zn(OH)2) is more stable making it an effective anodic barrier upon zinc. These precipitated oxides formed at pH 12 support cathodic reactions on their surface which in turn catalyse further oxide growth by a cathodically driven process. Focused ion beam-scanning electron microscopy (FIB-SEM) was used to support some of the electrochemical assertions, revealing the form and morphology of the passive layers that grow upon zinc exposed to alkaline solutions.

Description

Citation

Source

Electrochimica Acta

Book Title

Entity type

Publication

Access Statement

License Rights

Restricted until

abcd