Influence of ultrasound power and frequency upon corrosion kinetics of zinc in saline media.

This paper is devoted to zinc corrosion and oxidation mechanism in an ultrasonically stirred aerated sodium sulfate electrolyte. It follows a previous study devoted to the influence of 20 kHz ultrasound upon zinc corrosion in NaOH electrolytes [Ultrason. Sonochemis. 8 (2001) 291]. In the present work, various ultrasound regimes were applied by changing the transmitted power and the wave frequency (20 and 40 kHz). Unlike NaOH electrolyte which turns the zinc electrode into a passive state, Na2SO4 saline media induces soft corrosion conditions. This allows a study of the combined effects of ultrasonically modified hydrodynamic and mechanical damage (cavitation) upon the zinc corrosion process. A series of initial experiments were carried out so as to determine the transmitted power and to characterize mass transfer distribution in the electrochemical cell. Zinc corrosion and oxidation process were subsequently studied with respect to the vibrating parameters. When exposed to a 20 kHz ultrasonic field, and provided that the electrode is situated at a maximum mass transfer point, the corrosion rate reaches values six to eight times greater than in silent conditions. The zinc oxidation reaction, in the absence of competitive reduction reactions, is also activated by ultrasound (20 and 40 kHz) but probably through a different process of surface activation.

[1]  C. Deslouis,et al.  The kinetics of zinc dissolution in aerated sodium sulphate solutions. A measurement of the corrosion rate by impedance techniques , 1989 .

[2]  B. Harvey,et al.  Preliminary investigation of the ultrasonically enhanced corrosion of stainless steel in the nitric acid/chloride system , 1996 .

[3]  B. Harvey,et al.  Ultrasonically enhanced corrosion of 304L stainless steel II: the effect of frequency, acoustic power and horn to specimen distance. , 1997, Ultrasonics sonochemistry.

[4]  J. Hihn,et al.  Electrochemical behaviour of zinc in 20 kHz sonicated NaOH electrolytes. , 2001, Ultrasonics sonochemistry.

[5]  A. Wilhelm,et al.  Electrochemical determination of the active zones in a high-frequency ultrasonic reactor , 1996 .

[6]  T. Mason,et al.  Applied Sonochemistry: The Uses of Power Ultrasound in Chemistry and Processing , 2002 .

[7]  Honghua Zhang,et al.  Effects of high-intensity ultrasound on glassy carbon electrodes , 1993 .

[8]  Stefano Mischler,et al.  Electrochemical methods in tribocorrosion: a critical appraisal , 2001 .

[9]  Timothy J. Mason,et al.  Quantifying sonochemistry: Casting some light on a ‘black art’ , 1992 .

[10]  J. Hihn,et al.  The effects of 20 kHz and 500 kHz ultrasound on the corrosion of zinc precoated steels in [Cl−] [SO2−4] [HCO−3] [H2O2] electrolytes , 2001 .

[11]  F. Marken,et al.  Sonoelectrochemical and sonochemical effects of cavitation: correlation with interfacial cavitation induced by 20 kHz ultrasound. , 2000, Ultrasonics sonochemistry.

[12]  J. Einhorn Advances in sonochemistry: Edited by T.J. Mason JAI Press, 1990 , 1991 .

[13]  Evan Cooper,et al.  Mass Transport in Sonovoltammetry with Evidence of Hydrodynamic Modulation from Ultrasound , 1998 .

[14]  W. Tomlinson,et al.  Erosion and corrosion of pure iron under cavitating conditions , 1991 .

[15]  H. Shalaby,et al.  Cavitation Corrosion Behavior of Cast Nickel-Aluminum Bronze in Seawater , 1995 .