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Evaluation of the corrosion resistance of electroless Ni-P and Ni-P composite coatings by electrochemical impedance spectroscopy

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TLDR
In this paper, the same fundamental reaction is occurring on all the coatings of the present study but over a different effective area in each case, which can be attributed to the decrease in the effective metallic area prone to corrosion.
Abstract
Electroless Ni-P composite coatings have gained a good deal of popularity and acceptance in recent years as they provide considerable improvement of desirable qualities such as hardness, wear, abrasion resistance, etc. The disagreement among researchers on the corrosion behaviour of these coatings warrants a thorough investigation. Among the various techniques available for the determination of corrosion resistance, electrochemical impedance spectroscopy (EIS) is considered to be superior as it provides not only an assessment of the corrosion resistance of different deposits but also enables the mechanistic pathway by which the deposits become corroded to be determined. The present investigation focuses on the evaluation of the corrosion resistance of electroless Ni-P and Ni-P-Si3N4, Ni-P-CeO2 and Ni-P-TiO2 composite coatings produced using an acidic hypophosphite-reduced electroless nickel bath, using EIS. The study makes evident that the same fundamental reaction is occurring on all the coatings of the present study but over a different effective area in each case. The charge transfer resistance of electroless Ni-P and Ni-P composite deposits are in the range 32,253–90,700 Ω cm2, whereas the capacitances of these coatings are in the range 11–17 µF/cm2. The improved corrosion resistance obtained for electroless Ni-P and Ni-P composite coatings is due to the enrichment of phosphorus on the electrode surface, which enables the preferential hydrolysis of phosphorus over that of nickel. The better corrosion resistance obtained for electroless Ni-P composite coatings can be ascribed to the decrease in the effective metallic area prone to corrosion. Among the three electroless Ni-P composite coatings, the corrosion resistance is in the following order: Ni-P-CeO2=Ni-P-Si3N4>Ni-P-TiO2.

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Citations
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Journal ArticleDOI

Metallic composite coatings by electroless technique – a critical review

TL;DR: In this paper, the authors reviewed the recent developments in micro and nanostructured metallic composite coatings formed by electroless coating techniques and retrospect into the various mechanisms of the electroless process, its preparation with different metallic systems, properties, and applications in detail.
Journal ArticleDOI

Synthesis of a duplex Ni-P-YSZ/Ni-P nanocomposite coating and investigation of its performance

TL;DR: In this article, a duplex Ni P with yttria-fully stabilised zirconia (YSZ) nanoparticle composite coating was prepared by electroless deposition on a carbon steel substrate.
Journal ArticleDOI

The corrosion behavior of electroless Ni–P coating in Cl−/H2S environment

TL;DR: In this paper, an amorphous state Ni-P coating was prepared by electroless plating method in order to improve the corrosion resistance of refinery heat exchanger at low temperature.
Journal ArticleDOI

Electrodeposition and corrosion resistance of Ni–P–TiN composite coating on AZ91D magnesium alloy

TL;DR: In order to improve the corrosion resistance and micro-hardness of AZ91D magnesium alloy, TiN nanoparticles were added to fabricate Ni-P-TiN composite coating by electrodeposition.
Journal ArticleDOI

Effect of SiO2 and PTFE additives on dry sliding of NiP electroless coating

TL;DR: In this article, the effect of silicon dioxide and polytetrafluoroethylene (PTFE) additives on NiP coating performance under dry (unlubricated) conditions in unidirectional and reciprocating sliding modes in Ball-on-Flat configuration.
References
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Journal ArticleDOI

The anodic behavior of amorphous Ni-19P alloys in different amorphous states

TL;DR: In this article, an amorphous Ni-19P alloy prepared by rapid quenching of white heat melt showed a higher anodic dissolution current density in 1 N HCl in comparison with the same amorphized alloy prepared with red heat melt, showing that the difference in anodic behavior between these two as-quenched specimens seems due to the differences in the amounts of quenched-in defects.
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