Doche M-L, Hihn J-Y, Mandroyan A, Viennet R, Touyeras F
Laboratoire de Chimie des Matériaux et Interfaces-Equipe de l'IUT, BP 1559, 30 av. de l'Observatoire, 25009 Besançon Cedex, France.
Ultrason Sonochem. 2003 Oct;10(6):357-62. doi: 10.1016/S1350-4177(03)00099-3.
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.
本文致力于研究超声搅拌充气硫酸钠电解液中锌的腐蚀和氧化机理。它延续了之前一项关于20 kHz超声波对锌在氢氧化钠电解液中腐蚀影响的研究[《超声化学》8 (2001) 291]。在本工作中,通过改变发射功率和波频率(20 kHz和40 kHz)应用了各种超声模式。与使锌电极进入钝态的氢氧化钠电解液不同,硫酸钠盐介质会引发轻度腐蚀条件。这使得能够研究超声改性流体动力学和机械损伤(空化)对锌腐蚀过程的综合影响。进行了一系列初始实验以确定发射功率并表征电化学电池中的传质分布。随后针对振动参数研究了锌的腐蚀和氧化过程。当暴露于20 kHz超声场且电极位于最大传质点时,腐蚀速率达到比无超声条件下大六至八倍的值。在没有竞争性还原反应的情况下,锌的氧化反应也会被超声(20 kHz和40 kHz)激活,但可能是通过不同的表面活化过程。