scholarly journals Corrosion Resistance of Heat-Treated Ni-W Alloy Coatings

Materials ◽  
2020 ◽  
Vol 13 (5) ◽  
pp. 1172
Author(s):  
Magdalena Popczyk ◽  
Julian Kubisztal ◽  
Andrzej Szymon Swinarew ◽  
Zbigniew Waśkiewicz ◽  
Arkadiusz Stanula ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Corrosion Resistance ◽  
Electrochemical Impedance ◽  
Active Surface ◽  
Active Surface Area ◽  
X Ray Diffraction ◽  
Kelvin Probe ◽  
Research On Evaluation ◽  
Heat Treated ◽  
Electrochemically Active

The paper presents research on evaluation of corrosion resistance of Ni-W alloy coatings subjected to heat treatment. The corrosion resistance was tested in 5% NaCl solution by the use of potentiodynamic polarization technique and electrochemical impedance spectroscopy. Characteristics of the Ni-W coatings after heat treatment were carried out using scanning electron microscopy, scanning Kelvin probe technique and X-ray diffraction. Suggested reasons for the improvement of properties of the heat treated Ni-W coating, obtained at the lowest current density value (125 mA∙cm−2), are the highest tungsten content (c.a. 25 at.%) as well as the smallest and the most homogeneous electrochemically active surface area.

EFFECT OF HEAT TREATMENT ON MICROSTRUCTURE AND CORROSION RESISTANCE OF Ni-B-W-Mo COATING DEPOSITED BY ELECTROLESS METHOD

2018 ◽  
Vol 25 (08) ◽  
pp. 1950023 ◽  
Author(s):  
ARKADEB MUKHOPADHYAY ◽  
TAPAN KUMAR BARMAN ◽  
PRASANTA SAHOO
Keyword(s):  
Heat Treatment ◽  
Corrosion Resistance ◽  
Electrochemical Techniques ◽  
Sodium Molybdate ◽  
Medium Carbon Steel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Solid Solution Strengthening ◽  
Heat Treated ◽  
Electroless Coatings

The present work reports the deposition of a quaternary Ni-B-W-Mo coating on AISI 1040 medium carbon steel and its characterization. Quaternary deposits are obtained by suitably modifying existing electroless Ni-B bath. Composition of the as-deposited coating is analyzed by energy dispersive X-ray spectroscopy. The structural aspects of the as-deposited and coatings heat treated at 300[Formula: see text]C, 350[Formula: see text]C, 400[Formula: see text]C, 450[Formula: see text]C and 500[Formula: see text]C are determined using X-ray diffraction technique. Surface of the as-deposited and heat-treated coatings is examined using a scanning electron microscope. Very high W deposition could be observed when sodium molybdate is present in the borohydride-based bath along with sodium tungstate. The coatings in their as-deposited condition are amorphous while crystallization takes place on heat treatment. A nodulated surface morphology of the deposits is also observed. Vickers’ microhardness and crystallite size measurement reveal inclusion of W and Mo results in enhanced thermal stability of the coatings. Solid solution strengthening of the electroless coatings by W and Mo is also observed. The applicability of kinetic strength theory to the hardening of the coatings on heat treatment is also investigated. Corrosion resistance of Ni-B-W-Mo coatings and effect of heat treatment on the same are also determined by electrochemical techniques.

Structure and Corrosion Resistance of Iron Coatings Containing Silicon Powders

2011 ◽  
Vol 399-401 ◽  
pp. 1926-1931 ◽  
Author(s):  
Yi Wang ◽  
Gang Chen ◽  
Wei Dong Liu ◽  
Qiong Yu Zhou ◽  
Qing Dong Zhong
Keyword(s):  
Corrosion Resistance ◽  
Phase Composition ◽  
Thermal Treatment ◽  
Surface Morphology ◽  
Electrochemical Impedance ◽  
Electrochemical Corrosion ◽  
Active Surface ◽  
Active Surface Area ◽  
Two Phase ◽  
Electrochemical Corrosion Resistance

Fe + Si coatings were prepared by iron deposition from a bath containing a suspension of silicon powders. These coatings were obtained at galvanostatic conditions, at the current density of jdep=−0.020 A cm−2 and at the temperature of 338 K. For determination of the influence of phase composition and surface morphology of these coatings on changes in the corrosion resistance, these coatings were modified in an argon atmosphere by thermal treatment at 873 K for 2h. A scanning electron microscope was used for surface morphology characterization of the coatings. The chemical composition of the coatings was determined by EDS and phase composition investigations were conducted by X-ray diffraction. It was found that the as-deposited coatings consist of a two-phase structure, i.e., iron and silicon. The phase composition for the Fe + Si coatings after thermal treatment is markedly different. The main peaks corresponding to Fe and Si coexist with the new phases: FeSi. Electrochemical corrosion resistance investigations were carried out in 3.5wt% NaCl, using potentiodynamic and electrochemical impedance spectroscopy (EIS) methods. On the basis of these investigations it was found that the Fe + Si coatings after thermal treatment are more corrosion resistant in 3.5wt% NaCl solution than the as-deposited coatings. The reasons for this are a reduction in the amount of free iron and silicon, the presence of new phases (in particular silicides), and a decrease of the active surface area of the coatings after thermal treatment.

Wear and Corrosion Resistance of Electroless Nickel-Boron Coated Mild Steel

2010 ◽  
Vol 638-642 ◽  
pp. 846-851 ◽  
Author(s):  
Abdoul Fatah Kanta ◽  
Véronique Vitry ◽  
Fabienne Delaunois
Keyword(s):  
Heat Treatment ◽  
Corrosion Resistance ◽  
Mild Steel ◽  
Electrochemical Impedance ◽  
Electroless Nickel ◽  
Uncoated Steel ◽  
Wear And Corrosion ◽  
Heat Treated ◽  
Wear And Corrosion Resistance ◽  
Hardening Heat Treatment

Nickel-boron coatings were synthesized on mild steel by the electroless deposition method. Some of the coatings were submitted to a hardening heat treatment at 400°C during 1 hour in an atmosphere containing 95% Ar and 5% H2. Uncoated steel, treated and untreated samples were submitted to the Taber abrasion test to assess their wear resistance. The wear track was then examined by SEM and roughness measurement. The Taber Wear Index of untreated samples was slightly better than that of steel but heat treated samples attained TWI as small as 13. The corrosion resistance of the samples was investigated by the way of polarization and electrochemical impedance spectroscopy (EIS) and the influence of the heat treatment was observed.

scholarly journals Synthesis and Characterization of PdAgNi/C Trimetallic Nanoparticles for Ethanol Electrooxidation

Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2244
Author(s):  
Ahmed Elsheikh ◽  
James McGregor
Keyword(s):  
Photoelectron Spectroscopy ◽  
Electrochemical Impedance ◽  
Active Surface ◽  
Active Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Steady State Current ◽  
Xrd Patterns ◽  
Co Reduction

The direct use of ethanol in fuel cells presents unprecedented economic, technical, and environmental opportunities in energy conversion. However, complex challenges need to be resolved. For instance, ethanol oxidation reaction (EOR) requires breaking the rigid C–C bond and results in the generation of poisoning carbonaceous species. Therefore, new designs of the catalyst electrode are necessary. In this work, two trimetallic PdxAgyNiz/C samples are prepared using a facile borohydride reduction route. The catalysts are characterized by X-ray diffraction (XRD), Energy-Dispersive X-ray spectroscopy (EDX), X-ray photoelectron Spectroscopy (XPS), and Transmission Electron Microscopy (TEM) and evaluated for EOR through cyclic voltammetry (CV), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS). The XRD patterns have shown a weak alloying potential between Pd, and Ag prepared through co-reduction technique. The catalysts prepared have generally shown enhanced performance compared to previously reported ones, suggesting that the applied synthesis may be suitable for catalyst mass production. Moreover, the addition of Ag and Ni has improved the Pd physiochemical properties and electrocatalytic performance towards EOR in addition to reducing cell fabrication costs. In addition to containing less Pd, The PdAgNi/C is the higher performing of the two trimetallic samples presenting a 2.7 A/mgPd oxidation current peak. The Pd4Ag2Ni1/C is higher performing in terms of its steady-state current density and electrochemical active surface area.

Effect of Heat Treatment on Microstructure and Corrosion Resistance of Ni-P/BN(h) Composite Coatings

2011 ◽  
Vol 239-242 ◽  
pp. 3362-3366
Author(s):  
Cheng Zhang Peng ◽  
Ling Ling Zhu ◽  
You Ming Chen
Keyword(s):  
Heat Treatment ◽  
Corrosion Resistance ◽  
Composite Coatings ◽  
Stable State ◽  
Amorphous Structure ◽  
Treatment Temperature ◽  
X Ray Diffraction ◽  
Pulse Electroplating ◽  
Heat Treated ◽  
Precipitated Phases

The Ni-P/ BN(h) composite coatings were prepared by pulse electroplating,and were heat treated at temperature of 200～400°C.The microstructure of the composite coatings was identified by X-ray diffraction,the corrosion behavior of the composite coatings in 3.5%NaCl and 10%H2SO4 solutions was investigated by the linear polarization measurements and scanning electron microscope (SEM).The results show that the as-deposited is an amorphous structure,the precipitated phases are Ni12P5 and Ni5P2 metastable state phases when heat treatment temperature is below 300°C,the precipitated phases is Ni3P stable state phase heat-treated at 400°C，the composite coating was crystallized in great degree.Both the as-deposited and heat treated composite coatings revealed best corrosion resistance in 3.5%NaCl and 10%H2SO4 solutions.

Corrosion Resistance of Mo-Fe-Ti Alloy for Overpack in Simulating Underground Environment

2010 ◽  
Author(s):  
Toshiyasu Nishimura
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Corrosion Resistance ◽  
Electrochemical Impedance ◽  
Selective Dissolution ◽  
Immersion Test ◽  
Ti Alloy ◽  
Nacl Solution ◽  
Β Phase ◽  
Heat Treated

In order to examine the application of Mo-Fe-Ti alloy for overpak, the corrosion resistance of heat-treated its alloys was investigated by Electrochemical impedance spectroscopy (EIS), Field emission scanning electron microscopy (FE-SEM), Transmission electron microscopy (TEM) and Energy dispersive X-ray analysis (EDAX). Considering the welding, the sample subjected to solution heat treatment (ST) had a single β phase and samples subjected to aging heat treatment at 600–700°C had a-phase precipitation in b-phase. EIS results showed that the corrosion resistance of the aging heat-treated samples was lower than that of the ST sample, but much higher than that of pure Ti in long term immersion test in 10% NaCl solution of pH 0.5 at 97°C which simulating the crevice solution. Laser micrographs of the aging heat-treated samples indicated that a-phase at the grain boundary and in the grain was selectively corroded and caused selective dissolution in NaCl solution. The results of TEM combined with EDAX analyses showed that there were b-phase matrix composed of 2.7 wt% of Mo and 4.8wt% of Fe, and a-phase composed of 0.7 wt% of Mo and 0.1 wt% of Fe in sample aged at 600°C. Thus, Mo-poor a-phase was selectively dissolved in in 10% NaCl solution of pH 0.5 at 97°C. In a result, the ST sample of only b-phase showed the highest resistance, and aging heat-treated samples containing a-phase (0.7 wt% of Mo) showed higher values than pure Ti in the corrosion test. Addition of Fe did not decrease the resistance of alloy in the case of ST condition. Moreover, as Fe was involved in b-phase with Mo which increased remarkably the corrosion resistance, the addition of Fe did not decrease the corrosion resistance of aging heat-treated Mo-Fe-Ti alloy. Finally, it was concluded that Mo-Fe-Ti alloy had excellent resistance for overpack in simulating underground environment.

Production and Electrochemical Characterization of Nickel Based Composite Coatings Containing Chromium Group Metal and Silicon Powders

2015 ◽  
Vol 228 ◽  
pp. 219-224
Author(s):  
Magdalena Popczyk ◽  
Julian Kubisztal ◽  
Bożena Łosiewicz ◽  
A. Budniok
Keyword(s):  
Steady State ◽  
Electrode Materials ◽  
Electrochemical Impedance ◽  
Composite Coatings ◽  
Active Surface ◽  
Electrochemical Activity ◽  
Active Surface Area ◽  
Electrochemically Active ◽  
Electrochemically Active Surface

The Ni+Cr+Si, Ni+Mo+Si and Ni+W+Si composite coatings were obtained by electrodeposition of crystalline nickel from an electrolyte containing suspension of suitable metallic and non-metallic components (Cr, Mo, W and Si). These coatings were obtained galvanostatically at the current density of jdep = -0.100 A cm-2 and at the temperature of 338 K. Chemical composition of the coatings was determined by energy dispersive spectroscopy (EDS). The electrochemical activity of these electrocatalysts was studied in the process of hydrogen evolution reaction (HER) in 5 M KOH solution using steady-state polarization and electrochemical impedance spectroscopy (EIS) methods. The kinetic parameters of the HER on particular electrode materials were determined. It was found that Ni+Mo+Si composite coatings are characterized by enhanced electrochemical activity towards the HER as compared with Ni+W+Si and Ni+Cr+Si coatings due to the presence of Mo and increase in electrochemically active surface area.

Effect of Heat Treatment of AZ91 Magnesium Alloy on the Electroless Ni-P Deposition

2018 ◽  
Vol 1148 ◽  
pp. 122-127 ◽  
Author(s):  
Charu Singh ◽  
S.K. Tiwari ◽  
Raghuvir Singh
Keyword(s):  
Heat Treatment ◽  
Corrosion Resistance ◽  
Magnesium Alloy ◽  
Magnesium Alloys ◽  
Electrochemical Impedance ◽  
Cast Alloy ◽  
Az91 Magnesium Alloy ◽  
Heat Treated ◽  
Az91 Magnesium ◽  
Electroless Ni

Magnesium alloys are excellent choice for automobile, aerospace, and computer components owing to their light weight, unique physical and mechanical properties. However, poor corrosion resistance has restricted their applications in aggressive environments. The surface coating is one of the viable options to reduce the susceptibility of magnesium alloys to corrosion. The present study focuses on the effect of heat treatment of AZ91 magnesium alloy, for different durations at 400 °C, prior to electroless Ni-P deposition on corrosion resistance. The microstructure and elemental analysis of the heat-treated specimens are performed using SEM and EDS techniques respectively. It is observed that the duration of heat treatment has a significant effect on the surface morphology and microstructure of the alloy. The precipitates in the cast alloy (enriched with Mg and Al) fragmented and the transformed into a new Al and Zn rich phase, after 12 h heat treatment. The dissolution of precipitates, however, observed on heating further to 24 h and exhibited relatively a lesser corrosion current density. The dense electroless Ni-P deposition is formed on the alloy heat treated for 24 h. The corrosion behavior of the single Ni-P layer on the heat treated (for 12 h) and untreated alloy show a marked deterioration, as investigated by the anodic polarization and electrochemical impedance spectroscopy (EIS) techniques. Relatively a better corrosion performance is seen for the double-layer Ni-P deposition. The duplex layer coatings on the as cast and heat treated for 24 h at 400 °C substrates showed an improved corrosion resistance compared to that on the 12 h heat treated substrate.

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