Abstract

Corrosion resistance of AA1070 aluminium alloy (AA1070) was compared to AA1070 reinforced with alumina at weight composition (wt. %) of 5% and 10%, and grain size of 150 nm and 600 nm. Potentiodynamic polarization and open circuit potential analysis were employed in 0.0125 M H2SO4, 3.5% NaCl and 0.0125 M H2SO4-3.5% NaCl solutions. Data showed 0.0125 M H2SO4-3.5% NaCl solution was the most deleterious with peak corrosion rate value of 6.682 mm/y while 3.5% NaCl solution was the weakest with peak value of 0.084 mm/y. AA1070 at 5% (wt. %) and 150 nm particle size generally displayed the highest corrosion rate with values between 0.084 and 6.682 mm/y. However, visible decrease in corrosion rate occurred with increase in alumina weight fraction and particle size due to growth of the protective oxide on the composite and reduction of discontinuities to minimal values between 0.031 and 2.192 mm/y at 10% alumina weight fraction and 600 nm particle size. Cathodic and anodic reaction mechanisms significantly differs with respect to the electrolyte. Anodic reaction mechanism appeared under activation control in the sulphate-chloride and chloride solution, compared to cathodic reaction mechanism in the sulphate and sulphate-chloride solutions. Significant anodic degradation reaction was prevalent on the anodic polarization plot in the sulphate solution. Plots from open circuit potential analysis shows the composites and monolithic Al were the most thermodynamically stable in H2SO4 solution. In the sulphate-chloride solution, significant potential transients coupled with high corrosion tendency are conspicuous. The plot showed chaotic thermodynamic behaviour active passive transition behaviour of the passive film.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.