Summary: | Aluminum cathodes have long been used for the electrowinning of zinc from zinc sulfatesulfuric
acid electrolyte. Severe corrosion above the electrolyte/air interface limits the
life of aluminum cathodes to ca. 18-24 months for a 6 mm thick plate. The failure
characteristics of aluminum cathodes were analyzed using optical microscopy, scanning
electron microscopy, energy dispersive x-ray analysis, and x-ray diffraction analysis.
Three corrosion zones were identified: zone I below the electrolyte/air interface, zone II
0-40 mm above the electrolyte/air interface, and zone III 40-140 mm above the
electrolyte/air interface. Zone II experienced maximum corrosion damage in the form of
shallow, dense, cusp-like pitting. For a rejected aluminum plate, the corrosion damage in
zone II was ca. 80% reduction in plate thickness. The corrosion damage in zones I and III
was minor corresponding to ca. 10% reduction in plate thickness. The failure pattern of
aluminum cathodes and the factors causing variation in corrosion rate in the different
zones were studied.
Corrosion processes occurring under thin electrolyte film conditions limited the life of the
cathode plate. The influence of microstructure, chloride, and fluoride on the corrosion
susceptibility of aluminum cathodes was investigated in simulated and industrial
electrolytes using cyclic polarization, potentiodynamic polarization, potentiostatic,
galvanostatic, open circuit, and free immersion techniques. These techniques were
coupled with electron metallography and chemical analysis of test solutions. The
corrosion rate of the aluminum cathode plate decreased with increased pH and zinc
concentration. Titanium addition to the cathode plate undermined its corrosion resistance
in zone I by enhancing hydrogen evolution. In the presence of cathodic polarization,
fluoride activated zone I corrosion but had minimal effect on zone II corrosion. Chloride
had minimal effect on zone I corrosion; however, it strongly activated zone II corrosion
and was the primary factor responsible for plate failure. A mechanism through which
chloride acted on the aluminum cathode plate was proposed. === Applied Science, Faculty of === Materials Engineering, Department of === Graduate
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