Study of inhibition mechanism and efficiency of indole-5-carboxylic acid on corrosion of copper in aerated 0·5M H2 SO4

G. Quartarone, A. Zingales, T. Bellomi, D. Bortolato, G. Capobianco
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引用次数: 14

Abstract

Abstract Inhibition of the corrosion of copper in aerated 0·5M sulphuric acid solutions containing various concentrations of indole-5-carboxylic acid was studied in the temperature range 25–55°C using potentiodynamic curves (Tafel lines), weight loss, analytical methods, and determination of double layer capacitance. The corrosion rates reveal good corrosion inhibition, up to 95% in the concentration range of 1 × 10-4–4 × 10-3M. Tafel anodic slopes in inhibited acid solutions are considerably higher than those in uninhibited acid solutions. This points to a change in the corrosion mechanism of copper in the presence of indole-5-carboxylic acid. Under these conditions, copper could electro-oxidise primarily to Cu+ rather than to Cu2+, forming slightly soluble [Cu–(indole-5-carboxylic)n ]+(ads) complexes. Corrosion rates determined by the weight loss method in both the absence and presence of inhibitor are much higher (on average by a factor of about 6) than those obtained with the potentiodynamic method. This points to a limitation of the Tafel line extrapolation method in corrosion rate determination. The double layer capacitance–potential curves indicate considerable adsorption of the inhibitor over a wide potential range (-600 to +200 mV with regard to Ecorr ).
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吲哚-5-羧酸在掺气0·5M h2so4中对铜的缓蚀机理及缓蚀效率研究
摘要在25 ~ 55℃的温度范围内,采用动电位曲线(Tafel线)、失重、分析方法和双层电容测定等方法,研究了不同浓度吲哚-5-羧酸的0·5M硫酸溶液对铜的缓蚀作用。在1 × 10-4-4 × 10-3M浓度范围内,缓蚀率可达95%。抑制酸溶液中的Tafel阳极斜率明显高于未抑制酸溶液。这表明铜在吲哚-5-羧酸存在下的腐蚀机制发生了变化。在这些条件下,铜主要电氧化为Cu+而不是Cu2+,形成微溶的[Cu -(吲哚-5-羧酸)n]+(ads)配合物。在无缓蚀剂和有缓蚀剂的情况下,用失重法测定的腐蚀速率比用动电位法测定的要高得多(平均约为6倍)。这指出了塔菲尔线外推法测定腐蚀速率的局限性。双层电容-电位曲线表明,在较宽的电位范围内(Ecorr为-600至+200 mV),抑制剂有相当大的吸附作用。
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