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Purpose: The purpose of this study is to reveal the effect of nano-Al2O3 particle addition on the nucleation/growth kinetics, microhardness, wear resistance and corrosion resistance of Co–P–xAl2O3 nanocomposite plating. Design/methodology/approach: The kinetics and properties of Co–P–xAl2O3 nanocomposite plating prepared by electroplating were investigated by electrochemical measurements, scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, Vickers microhardness measurement, SRV5 friction and wear tester and atomic force microscopy. Findings: A 12 g/L nano-Al2O3 addition in the plating solution can transform the nucleation/growth kinetics of the plating from the 3D progressive model to the 3D instantaneous model. The microhardness of the plating increased with the increase of nano-Al2O3 content in plating. The wear resistance of the plating did not adhere strictly to Archard's law. An even and denser corrosion product film was generated due to the finer grains, with a high corrosion resistance. Originality/value: The effect of different nano-Al2O3 addition on the nucleation/growth kinetics and properties of Co–P–xAl2O3 nanocomposite plating was investigated, and an anticorrosion mechanism of Co–P–xAl2O3 nanocomposite plating was proposed. [ABSTRACT FROM AUTHOR]

Purpose: This paper aims to study the effect of Hg2+ on the corrosion behavior of Al–2%Zn coatings on AA5083 in 3.5 Wt.% NaCl solution. Design/methodology/approach: Potentiodynamic polarization and electrochemical impedance spectroscopy are used to investigate the effect of Hg2+ on the corrosion behavior. The surface and cross-sectional morphology are characterized by scanning electron microscopy and energy dispersive spectroscopy (EDS) to further reveal the corrosion mechanism of Hg2+. Findings: The results show that the corrosion behavior of the coating changes significantly as the concentration of Hg2+ increases from 5 to 30 μg/L. The corrosion production film can inhibit the corrosion process when Hg2+ concentration is in the range of 0.5–5 μg/L, while Hg2+ can promote the corrosion process significantly when its concentration reaches to 30 μg/L. The generation rate of dense oxide film on the coating surface is faster than dissolution rate when the concentration of Hg2+ is in the range of 0–5 μg/L, which makes the coating "self-healing" and thus slightly slows down the corrosion rate. The EDS analysis shows that excessive Hg2+ are preferentially deposited at locations with inhomogeneous electrochemical properties, which in turn accelerates corrosion. Originality/value: The corrosion resistance of Al-based coatings is significantly affected by Hg2+ in seawater. Thus, it is important to explain the corrosion mechanism of Al–2%Zn coatings under the combined effect of Hg2+ and Cl− in 3.5 Wt.% NaCl solution. [ABSTRACT FROM AUTHOR]