CORROSION RESISTANCE OF GALVANIC NICKEL DEPOSITS AND ELECTROCHEMICAL ACTIVITY OF THEIR CORROSION PRODUCTS

Dmytro Uschapovskyi, O. Linyucheva, G. Vasiliev, Oleksander Liniuchev, A. Kushmyruk, R. Redko, Gleb Pidvashetsky, Taras Kurochenko
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Abstract

D.Yu. Ushchapovskyi, A.I. Kushmyruk, G.S. Vasiliev, O.V. Linyucheva, R.M. Redko, O.G. Linyuchev, G.Yu. Pidvashetsky, T.A. Kurochenko CORROSION RESISTANCE OF GALVANIC NICKEL DEPOSITS AND ELECTROCHEMICAL ACTIVITY OF THEIR CORROSION PRODUCTS Background. Bright galvanic nickel coatings, with high sulphur content, are less corrosion resistant than matte. Bright nickel coatings are particularly susceptible to corrosion damage in conditions that simulate tropical humid climates and are characterized by the presence of acetic acid vapours. Objective. The purpose of the paper is to investigate: corrosion resistance of galvanic nickel deposits in concentrated acetic acid and its vapours, electrochemical activity of sulphide-containing corrosion products of bright nickel coatings. Methods. Potentiodynamic and cyclic volt-amperometry have been used to study the electrochemical activity of galvanic nickel deposits and their corrosion products. The corrosion rate of galvanic nickel deposits has been determined by gravimetric method. Investigation of surface morphology and composition of galvanic deposits were performed using scanning electron microscopy and X-ray fluorescence analysis. Results.The increased electrochemical activity of sulphide corrosion products of bright nickel coatings is evidenced by an order of magnitude higher cathodic current densities of CVA curves obtained in acetate buffer solutions, in comparison with bright and matte nickel galvanic deposits. It has been shown that at the deposition of sulphide corrosion products of bright nickel coatings on matte nickel foil the corrosion rate of last one increase at the exposition in concentrated acetic acid and its vapours. Conclusions. Significant intensifying effect of sulphur on the corrosion of galvanic nickel deposits in concentrated acetic acid and its vapours has been established. In particular, this can be explained by the decomposition of nickel sulphide (which incorporates in the coating) in acetic acid. Sulphur in the oxidation state (-2) interacts with passive oxide coatings to form an adsorbed monolayer, which leads to the transition of nickel to the active state. Further research will focus on a deeper study of the electrochemical properties of corrosion products of bright nickel coatings. Key words: nickel coatings, corrosion products, nickel sulphides, corrosion activity, catalyst.
电镍镀层的耐蚀性及其腐蚀产物的电化学活性
D.Yu.Ushchapovsky,A.I.Kushmyruk,G.S.Vasiliev,O.V.Linyucheva,R.M.Redko,O.G.Linyuchev,G.Yu.Pidvashetsky,T.A.Kurochenko镀锌镍镀层的耐蚀性及其腐蚀产物的电化学活性背景。光亮的电镀镍涂层含硫量高,耐腐蚀性不如亚光。明亮的镍涂层在模拟热带潮湿气候的条件下特别容易受到腐蚀损伤,其特征是存在乙酸蒸汽。客观的本文的目的是研究电镀镍镀层在浓乙酸及其蒸汽中的耐腐蚀性,光亮镍镀层含硫化物腐蚀产物的电化学活性。方法。采用恒电位法和循环伏安法研究了电镀镍镀层及其腐蚀产物的电化学活性。用重量法测定了电镀镍镀层的腐蚀速率。使用扫描电子显微镜和X射线荧光分析对电偶沉积物的表面形态和成分进行了研究。后果与光亮和哑光镍电镀沉积物相比,在乙酸盐缓冲溶液中获得的CVA曲线的阴极电流密度高出一个数量级,证明了光亮镍涂层的硫化物腐蚀产物的电化学活性增加。研究表明,光亮镍涂层的硫化物腐蚀产物在亚光镍箔上沉积时,在浓乙酸及其蒸汽中暴露时,最后一层的腐蚀速率增加。结论。硫对电镀镍镀层在浓乙酸及其蒸汽中的腐蚀具有显著的强化作用。特别是,这可以通过硫化镍(包含在涂层中)在乙酸中的分解来解释。处于氧化态(-2)的硫与钝化氧化物涂层相互作用,形成吸附的单层,这导致镍向活性态的转变。进一步的研究将集中在对光亮镍涂层腐蚀产物的电化学性能进行更深入的研究。关键词:镍涂层,腐蚀产物,硫化镍,腐蚀活性,催化剂。
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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