Role of chromium in anomalous behaviour of the passive layer in Ni-Cr-Mo alloys in 1M HCl solution

CORROSION ◽  
10.5006/3767 ◽  
2022 ◽  
Author(s):  
Malvika Karri ◽  
Amit Verma ◽  
J.B. Singh ◽  
Sunil Kumar Bonagani ◽  
U.K. Goutam

This work seeks to understand the underlying mechanism involved in passivity of Ni-Cr-Mo alloys in a less concentrated HCl solution (1M) by systematically varying contents of Cr and Mo solutes in model Ni-Cr-Mo alloys. Corrosion behaviour was evaluated based on potentiodynamic polarisation tests carried out in conjunction with electrochemical impedance and x-ray photoelectron spectroscopies of passive films that formed on alloys during their exposure to the HCl solution. Results have shown that an increase in Mo alone is not sufficient to improve the corrosion resistance of the alloys at lower concentrations of HCl. Optimum concentrations of Cr and Mo solutes have been found to be in the vicinity of ~17 wt.% Cr and ~19 wt.% Mo for superior corrosion resistance of the alloys. This was attributed to the protection of the Cr2O3 layer as a consequence of the enrichment of Mo6+ ions in the passive film in 1M HCl solution.


Metals ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 634
Author(s):  
Mohammad Reza Jandaghi ◽  
Abdollah Saboori ◽  
Gholamreza Khalaj ◽  
Mohammadreza Khanzadeh Ghareh Shiran

In this study, the microstructural evolutions and corrosion resistance of aluminium/copper joint fabricated through explosive welding process have been thoroughly investigated, while stand-off distance was variable. Microstructural analyses demonstrate that, regardless of grain refinement in the welding boundary, increasing the stand-off space is followed by a higher thickness of the localized melting pool. X-Ray diffraction (XRD) and energy-dispersive X-ray spectroscopy (EDS) analyses recognized the binary intermetallic layers as a combination of Al2Cu and AlCu. Polarization and electrochemical impedance spectroscopy (EIS) corrosion tests revealed that a higher stand-off distance resulted in the increment of corrosion potential, current rate, and concentration gradient at the interface owing to the remarkable kinetic energy of the collision, which impaired corrosion resistance.



Author(s):  
Abeens M ◽  
R Murugananthan

Abstract As AA 7075 T651 comprehensively is used in the marine naval vessels, the factor of corrosion performance always plays a significant role. In this work, an investigation is carried out to study the effect of corrosion behaviour of shot peened AA 7075 T651 in 3.5% solution. From the potentiodynamic polarization study, a 27.72% decrease is ascertained in the Icorr in shot peened specimen in correlation to unpeened aluminium alloy. A drop in Icorr from 1.883 to 1.480 mA/cm2 in shot peened specimen, indicates enhanced pitting corrosion resistance. An electrochemical impedance spectroscopy reveals a surge in the oxide layer formation on the peened surface aiding the drop in corrosion rate. Resistance to pit formations and improvement in oxygen deposition in the peened specimen is observed availing a Scanning Electron Microscopy (SEM) and Energy Dispersive X-Ray analysis (EDX). The micro structures of the peened and unpeened specimen are captured using optical microscopy and Transmission electron microscopy (TEM). Micro-strain, dislocation density is also calculated from the X- ray diffraction analysis (XRD), in which grain size reduces by 28.07%, dislocation density surges by 38.65% and micro strain increases by 21.95% in peened specimen in correlation to unpeened AA 7075 T651, resulting in a surge in corrosion resistance by 27.92% in the peened specimen in correlation to unpeened aluminium alloy.



2012 ◽  
Vol 12 ◽  
pp. 139-148
Author(s):  
Jagadeesh Bhattarai

The role of a simultaneous additions of tungsten and tantalum on the anodic passivity of the passive films of the sputter-deposited nanocrystalline W-xTa alloys was studied using immersion tests, electrochemical measurements and X-ray photoelectron spectroscopic (XPS) analysis. The formation of spontaneous passive film on the alloys, which is composed of double oxyhydroxide of tungsten and tantalum ions are responsible for their higher corrosion resistance than those of the alloy-constituting elements in 12 M HCl solution open to air at 30°C. The quantitative surface analysis by XPS is clarified that the improved anodic passivity of the alloys than those of alloy-constituting elements is based on the formation of new anodic passive oxyhydroxide films composed of W6+ and Ta5+ ions. These films have higher protectiveness and stability than those of passive oxyhydroxide films of alloy-constituting elements, that is, oxyhydroxides of hexavalent tungsten and pentavalent tantalum after potentiostatic polarization for 1 h in 12 M HCl.DOI: http://dx.doi.org/10.3126/njst.v12i0.6492 Nepal Journal of Science and Technology 12 (2011) 139-148 



2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Nady ElSayed ◽  
Mohamed M. El-Rabiei ◽  
Mosaad Negem

Abstract Electroplated protective thin film is highly promising materials for advanced applications such as high corrosion resistance and energy conversion and storage. This work is to investigate the effect of Co content and TiO2 on the corrosion resistance of Ni–xCo–yTiO2 nanocomposites in alkaline media. The nanocrystalline Ni–xCo–yTiO2 composites were electroplated using the sulfate-gluconate bath containing the suspended TiO2 nanograins under ultrasound waves and mechanical stirring. The microstructure and corrosion behavior of the electroplated Ni–xCo–yTiO2 nanocomposites have been investigated via X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) techniques. The XRD pattern of the electroplated Ni–Co matrices with 1–75% of cobalt arranged in face-centered cubic (FCC) system, while the electroplated Ni–Co matrices of further Co% more than 76% converted to hexagonal closed-package (HCP) crystal system. The surface of the Ni–xCo–yTiO2 nanocomposites after immersion in 1.0 M KOH electrolytes was investigated via SEM, atomic force microscopy and EDX. The results displayed that the rate of corrosion of the different composites decreased by combining Ni, Co and the inclusion of TiO2. The improved corrosion resistance of Ni–47Co–3.77TiO2 composites is due to the formation of Ni/Co oxy/hydroxide layer and rebelling effect of OH− by TiO2 sites, which reduces the attacking effect of OH−, O2, and H2O, and notably retards the overall corrosion processes.



Materials ◽  
2019 ◽  
Vol 12 (8) ◽  
pp. 1233 ◽  
Author(s):  
Nader El-Bagoury ◽  
Sameh I. Ahmed ◽  
Ola Ahmed Abu Ali ◽  
Shimaa El-Hadad ◽  
Ahmed M. Fallatah ◽  
...  

The effect of microstructure and chemistry on the kinetics of passive layer growth and passivity breakdown of some Ti-based alloys, namely Ti-6Al-4V, Ti-6Al-7Nb and TC21 alloys, was studied. The rate of pitting corrosion was evaluated using cyclic polarization measurements. Chronoamperometry was applied to assess the passive layer growth kinetics and breakdown. Microstructure influence on the uniform corrosion rate of these alloys was also investigated employing dynamic electrochemical impedance spectroscopy (DEIS). Corrosion studies were performed in 0.9% NaCl solution at 37 °C, and the obtained results were compared with ultrapure Ti (99.99%). The different phases of the microstructure were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Chemical composition and chemistry of the corroded surfaces were studied using X-ray photoelectron spectroscopy (XPS) analysis. For all studied alloys, the microstructure consisted of α matrix, which was strengthened by β phase. The highest and the lowest values of the β phase’s volume fraction were recorded for TC21 and Ti-Al-Nb alloys, respectively. The susceptibility of the investigated alloys toward pitting corrosion was enhanced following the sequence: Ti-6Al-7Nb < Ti-6Al-4V << TC21. Ti-6Al-7Nb alloy recorded the lowest pitting corrosion resistance (Rpit) among studied alloys, approaching that of pure Ti. The obvious changes in the microstructure of these alloys, together with XPS findings, were adopted to interpret the pronounced variation in the corrosion behavior of these materials.



Author(s):  
Nader El-Bagoury ◽  
Sameh Ibrahim ◽  
Ola Ahmed Abu Ali ◽  
Shimaa El-Hadad ◽  
Ahmed M. Fallatah ◽  
...  

The effect of microstructure and chemistry of passive films on the kinetics of passive layer growth and passivity breakdown of some Ti-based alloys, namely Ti-6Al-4V, Ti-6Al-7Nb and TC21 alloys was studied. The rate of pitting corrosion was evaluated using cyclic polarization measurements. Chronoamperometry was applied to assess the passive layer growth kinetics and breakdown. Microstructure influence on the uniform corrosion rate of these alloys was also investigated employing Tafel extrapolation and dynamic electrochemical impedance spectroscopy. Corrosion studies were performed in 0.9% NaCl solution at 37 oC, and the obtained results were compared with ultrapure Ti (99.99%). The different phases of the microstructure were characterized by X-ray diffraction and scanning electron microscopy. Chemical composition and chemistry of the corroded surfaces were studied using X-ray photoelectron analysis. For all studied alloys, the microstructure consisted of &alpha; matrix, which was strengthened by &beta; phase. The highest and the lowest values of the &beta; phase&rsquo;s volume fraction were recorded for TC21 and Ti-Al-Nb alloys, respectively. The uniform corrosion rate and pitting corrosion resistance (Rpit) of the studied alloys were enhanced following the sequence: Ti-6Al-7Nb &lt; Ti-6Al-4V &lt;&lt; TC21. The corrosion resistance of Ti-Al-Nb alloy approached that of pure Ti. The obvious changes in the microstructure of these alloys, together with XPS findings, were adopted to interpret the pronounced variation in their corrosion rates.



Metals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 89
Author(s):  
Wei Yuan ◽  
Qian Hu ◽  
Jiao Zhang ◽  
Feng Huang ◽  
Jing Liu

This study modified graphene oxide (GO) with hydrophilic octadecylamine (ODA) via covalent bonding to improve its dispersion in silicone-modified epoxy resin (SMER) coatings. The structural and physical properties of ODA-GO were characterized by field-emission scanning electron microscopy (FE-SEM), X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and contact angle tests. The ODA-GO composite materials were added to SMER coatings by physical mixing. FE-SEM, water absorption, and contact angle tests were used to evaluate the physical properties of the ODA-GO/SMER coatings, while salt spray, electrochemical impedance spectroscopy (EIS), and scanning Kelvin probe (SKP) methods were used to test the anticorrosive performance of ODA-GO/SMER composite coatings on Q235 steel substrates. It was found that ODA was successfully grafted onto the surfaces of GO. The resulting ODA-GO material exhibited good hydrophobicity and dispersion in SMER coatings. The anticorrosive properties of the ODA-GO/SMER coatings were significantly improved due to the increased interfacial adhesion between the nanosheets and SMER, lengthening of the corrosive solution diffusion path, and increased cathodic peeling resistance. The 1 wt.% ODA-GO/SMER coating provided the best corrosion resistance than SMER coatings with other amounts of ODA-GO (including no addition). After immersion in 3.5 wt.% NaCl solution for 28 days, the low-frequency end impedance value of the 1 wt.% ODA-GO/SMER coating remained high, at 6.2 × 108 Ω·cm2.



Metals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 704
Author(s):  
Marija Riđošić ◽  
Nebojša D. Nikolić ◽  
Asier Salicio-Paz ◽  
Eva García-Lecina ◽  
Ljiljana S. Živković ◽  
...  

Electrodeposition and characterization of novel ceria-doped Zn-Co composite coatings was the main goal of this research. Electrodeposited composite coatings were compared to pure Zn-Co coatings obtained under the same conditions. The effect of two ceria sources, powder and home-made sol, on the morphology and corrosion resistance of the composite coatings was determined. During the electrodeposition process the plating solution was successfully agitated in an ultrasound bath. The source of the particles was found to influence the stability and dispersity of plating solutions. The application of ceria sol resulted in an increase of the ceria content in the resulting coating and favored the refinement from cauliflower-like morphology (Zn-Co) to uniform and compact coral-like structure (Zn-Co-CeO2 sol). The corrosion resistance of the composite coatings was enhanced compared to bare Zn-Co as evidenced by electrochemical impedance spectroscopy and scanning Kelvin probe results. Zn-Co doped with ceria particles originating from ceria sol exhibited superior corrosion resistance compared to Zn-Co-CeO2 (powder) coatings. The self-healing rate of artificial defect was calculated based on measured Volta potential difference for which Zn-Co-CeO2 (sol) coatings exhibited a self-healing rate of 73.28% in a chloride-rich environment.



Metals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 852
Author(s):  
Asiful H. Seikh ◽  
Hossam Halfa ◽  
Mahmoud S. Soliman

Molybdenum (Mo) is an important alloying element in maraging steels. In this study, we altered the Mo concentration during the production of four cobalt-free maraging steels using an electroslag refining process. The microstructure of the four forged maraging steels was evaluated to examine phase contents by optical microscopy, scanning electron microscopy (SEM), and X-ray diffraction (XRD) analysis. Additionally, we assessed the corrosion resistance of the newly developed alloys in 3.5% NaCl solution and 1 M H2SO4 solution through potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) techniques. Furthermore, we performed SEM and energy-dispersive spectroscopy (EDS) analysis after corrosion to assess changes in microstructure and Raman spectroscopy to identify the presence of phases on the electrode surface. The microstructural analysis shows that the formation of retained austenite increases with increasing Mo concentrations. It is found from corrosion study that increasing Mo concentration up to 4.6% increased the corrosion resistance of the steel. However, further increase in Mo concentration reduces the corrosion resistance.



2005 ◽  
Vol 11 (S03) ◽  
pp. 82-85 ◽  
Author(s):  
E. T. Uzumaki ◽  
C. S. Lambert ◽  
A. R. Santos Jr. ◽  
C. A. C. Zavaglia

Diamond-like carbon (DLC) films have been intensively studied with a view to improving orthopaedic implants. Studies have indicated smoothness of the surface, low friction, high wear resistance, corrosion resistance and biocompatibility [1-4]. DLC coatings can be deposited using various techniques, such as plasma assisted chemical vapour deposition (PACVD), magnetron sputtering, laser ablation, and others [5]. However it has proved difficult to obtain films which exhibit good adhesion. The plasma immersion process, unlike the conventional techniques, allows the deposition of DLC on three-dimensional workpieces, even without moving the sample, without an intermediate layer, and with high adhesion [6], an important aspect for orthopaedic articulations. In our previous work, DLC coatings were deposited on silicon and Ti-13Nb-13Zr alloy substrates using the plasma immersion process for the characterization of microstructure, mechanical properties and corrosion behaviour [7-9]. Hardness, measured by a nanoindenter, ranged from 16.4-17.6 GPa, the pull test results indicate the good adhesion of DLC coatings to Ti-13Nb-13Zr, and electrochemical assays (polarization test and electrochemical impedance spectroscopy) indicate that DLC coatings produced by plasma immersion can improve the corrosion resistance [9].



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