Early stages of copper protection in chloride solution containing ferrous sulphate

A. E. El Warraky
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引用次数: 3

Abstract

Abstract The films formed on Cu surfaces in 4% NaCl with 10 ppm FeSO4 solution for short immersion times of up to 4 h were analysed using X-ray photoelectron spectroscopy and Auger electron spectroscopy. Iron was detected on the copper surface after immersion for 30 min. The presence of Fe(OH)2 and α-FeOOH species on the surface supports the proposal that Fe2+ ions are transported to the cathodic sites to form Fe(OH)2 which is subsequently oxidised to α-FeOOH (lepidocrocite) by dissolved oxygen in solution. The presence of a peak corresponding to the approximate empirical formula HCuFe2O10 suggests that the iron is incorporated into Cu2O which is formed at the moment of immersion. Both the Fe/Cu ratio on the surface and the film thickness increased with increasing time of immersion up to 2 h and then decreased again because it depends on the concentration of dissolved oxygen in solution and the residual amount of Fe2+ in solution.
在含硫酸亚铁的氯化物溶液中保护铜的早期阶段
用x射线光电子能谱和俄歇能谱分析了Cu表面在4% NaCl和10 ppm FeSO4溶液中短时间浸泡4 h后形成的薄膜。浸渍30 min后,在铜表面检测到铁。表面存在Fe(OH)2和α-FeOOH,这支持了Fe2+离子被输送到阴极位置形成Fe(OH)2,然后被溶液中的溶解氧氧化成α-FeOOH (lepidococite)。与近似实验式HCuFe2O10相对应的峰的存在表明,铁与浸出瞬间形成的Cu2O结合在一起。表面Fe/Cu比和膜厚均随浸液时间的增加而增大,但随着浸液时间的增加,膜厚又随着浸液时间的增加而减小,这主要取决于溶液中溶解氧的浓度和溶液中Fe2+的残留量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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