scholarly journals Corrosion and Corrosion Inhibition of High Strength Low Alloy Steel in 2.0 M Sulfuric Acid Solutions by 3-Amino-1,2,3-triazole as a Corrosion Inhibitor

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
El-Sayed M. Sherif ◽  
Adel Taha Abbas ◽  
D. Gopi ◽  
A. M. El-Shamy
Keyword(s):  
Sulfuric Acid ◽  
Corrosion Inhibition ◽  
Polarization Resistance ◽  
Immersion Time ◽  
Electrochemical Impedance ◽  
Hsla Steel ◽  
Electrochemical Techniques ◽  
High Strength ◽  
X Ray ◽  
Sulfuric Acid Solutions

The corrosion and corrosion inhibition of high strength low alloy (HSLA) steel after 10 min and 60 min immersion in 2.0 M H2SO4solution by 3-amino-1,2,4-triazole (ATA) were reported. Several electrochemical techniques along with scanning electron microscopy (SEM) and energy dispersive X-ray (EDS) were employed. Electrochemical impedance spectroscopy indicated that the increase of immersion time from 10 min to 60 min significantly decreased both the solution and polarization resistance for the steel in the sulfuric acid solution. The increase of immersion time increased the anodic, cathodic, and corrosion currents, while it decreased the polarization resistance as indicated by the potentiodynamic polarization measurements. The addition of 1.0 mM ATA remarkably decreased the corrosion of the steel and this effect was found to increase with increasing its concentration to 5.0 mM. SEM and EDS investigations confirmed that the inhibition of the HSLA steel in the 2.0 M H2SO4solutions is achieved via the adsorption of the ATA molecules onto the steel protecting its surface from being dissolved easily.

The influence of Ni on the microstructure and corrosion resistance of high-strength low alloy steel in the Cl-containing environment

2021 ◽  
Vol ahead-of-print (ahead-of-print) ◽  
Author(s):  
Dan Wang ◽  
Qingdong Zhong ◽  
Jian Yang ◽  
Shujian Zhang
Keyword(s):  
Corrosion Resistance ◽  
Alloy Steel ◽  
Photoelectron Spectroscopy ◽  
Hsla Steel ◽  
Electrochemical Techniques ◽  
High Strength ◽  
Low Alloy Steel ◽  
Transfer Resistance ◽  
Content Type ◽  
X Ray

Purpose This paper aims to search the optimum content of Ni on the microstructure, phase and electrochemical behavior of high-strength low alloy (HSLA) steel in the 3.5 wt.% NaCl solution. Design/methodology/approach The microstructure and corrosion resistance of Ni-containing HSLA steel in the simulated marine environment was studied by optical microscopy, scanning electron microscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and electrochemical techniques. Findings The sample containing 3.55 wt.% of nickel exhibited a finer grain size of 10 μm and a lower icorr of 2.169 µA cm−2. The XRD patterns showed that the Fe-Cr-Ni solid solution, FeC and Cr3C2 were observed in samples when Ni was added. Besides, the 3.55 wt.% of nickel addition enhanced the charge transfer resistance of the low alloy steel which suggested the sample possessed excellent inhibition of electrochemical reaction and corrosion resistance. The XPS spectrum suggested that nickel was beneficial to improve the corrosion resistance of steel by forming protective oxides, and the ratio of Fe2+/Fe3+ in protective oxides was increased. Practical implications Finding the comprehensive performance of HSLA steel which can be applied to unmanned surface vehicles in marine operations. Originality/value This study has a guiding significance for optimizing the composition of HSLA steel in a Cl- containing environment.

scholarly journals Corrosion Resistance of Hard Coat Anodized AA 6061 in Citric–Sulfuric Solutions

Coatings ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 601
Author(s):  
José Cabral-Miramontes ◽  
Citlalli Gaona-Tiburcio ◽  
Francisco Estupinán-López ◽  
María Lara-Banda ◽  
Patricia Zambrano-Robledo ◽  
...  
Keyword(s):  
Corrosion Resistance ◽  
Sulfuric Acid ◽  
Electrochemical Impedance ◽  
Electrochemical Techniques ◽  
Sulfuric Acid Electrolyte ◽  
Cyclic Potentiodynamic Polarization ◽  
Anodization Process ◽  
Current Densities ◽  
Corrosive Environments ◽  
Sulfuric Acid Solutions

Aluminum is a material widely used in aeronautical and transport industries due to its excellent mechanical and corrosion resistance properties. Unfortunately, aluminum alloys are susceptible to corrosion, which limits their use in some corrosive environments. The aim of this work is to characterize hard coat film fabricated by anodizing in a citric–sulfuric acid system using electrochemical techniques. The anodization process was carried out using an aluminum alloy AA 6061 anodization bath: a mix of citric and sulfuric acid solutions were used. For the anodizing process, two current densities were used, 1 and 7.2 A·cm−2. Anodized specimens obtained under different conditions were exposed to a 3.5 wt.% NaCl solution, and their electrochemical behavior was studied by electrochemical impedance spectroscopy (EIS) and cyclic potentiodynamic polarization (CPP) according to ASTM G106-15 and ASTM G5-13, respectively. Scanning electron microscopy (SEM) was employed to determinate the morphology and thickness of coatings. The results showed improved corrosion resistance in 6061 aluminum anodized in citric–sulfuric acid electrolyte compared to those anodized in sulfuric acid solution.

scholarly journals Evaluación de la degradación de superficies de fluorapatita mediante técnicas electroquímicas. (Degradation Assessment of Fluorapatite Surfaces using Electrochemical Techniques)

2015 ◽  
Vol 6 (1) ◽  
pp. 33 ◽  
Author(s):  
L. J. Reyes Jaimes ◽  
H. A. González Romero ◽  
A. Sandoval Amadora ◽  
D. Y. Peña Ballesteros ◽  
H. A. Estupiñán Durán
Keyword(s):  
Simulated Body Fluid ◽  
Body Fluid ◽  
Immersion Time ◽  
Electrochemical Impedance ◽  
Electrochemical Techniques ◽  
Active Surface ◽  
Apatite Formation ◽  
X Ray ◽  
Cathodic Electrodeposition ◽  
High Concentrations

ResumenSe evaluó el efecto del pH de fluido corporal simulado en la formación de apatitas y en la degradación de superficies de la aleación Ti6Al4V recubiertas con Fosfato de Calcio mediante la técnica de lectrodeposición catódica. Como variables de estudio se tomaron el pH del fluido corporal simulado y el tiempo de inmersión de los recubrimientos. Mediante microscopia electrónica de barrido, espectroscopia de energía dispersiva, difracción de rayos X y absorción atómica se pudo corroborar la formación de apatitas, y la degradación de los recubrimientos se evaluó mediante Espectroscopia de impedancia electroquímica y curvas de polarización potenciodinámicas. Los resultados obtenidos muestran que los recubrimientos tenían altas concentraciones de Fluorapatita (Ca5(PO4)3F) y que su formación se ve favorecida a medida que el pH del fluido corporal simulado y el tiempo de inmersión aumenta. Por otra parte, se obtuvo que las muestras evaluadas a pH de 7,2 son menos estables termodinámicamente, sin embargo, las evaluadas a 7,6 presentan una superficie más activa, por lo que se obtiene una mayor velocidad de degradación. AbstractThe pH eect of a Simulated Body Fluid in the apatite formation and the degradation of the Ti6Al4V alloy surfaces, coated by calcium phosphate obtained through cathodic electrodeposition was evaluated. The simulated body fluid pH and the coating immersion time were taken as variables. The formation of apatite was corroborated by Scanning Electron Microscopy, Energy Dispersive Spectroscopy, X Ray Diraction and Atomic Absorption Techniques. The coating degradation was assessed by the Electrochemical Impedance Spectroscopy and the Potential Dynamic Polarization Curves. The results have shown that the coatings had high concentrations of fluorapatite (Ca5(PO4)3F) and its formation was favored as the simulated body fluid pH and the immersion time increases. Moreover, it was found that the coatings samples evaluated at pH 7.2 were less thermodynamically steady, however, the evaluated coating at pH 7.6 exhibited a more active surface, so that a higher rate of degradation is obtained.

scholarly journals Effects of Immersion Time and 5-Phenyl-1H-tetrazole on the Corrosion and Corrosion Mitigation of Cobalt Free Maraging Steel in 0.5 M Sulfuric Acid Pickling Solutions

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
El-Sayed M. Sherif ◽  
Asiful H. Seikh
Keyword(s):  
Maraging Steel ◽  
Electron Spectroscopy ◽  
Polarization Resistance ◽  
Immersion Time ◽  
Electrochemical Impedance ◽  
Steel Corrosion ◽  
Polarization Data ◽  
Exposure Test ◽  
X Ray ◽  
Scanning Electron

The effect of exposure time and 5-phenyl-1H-tetrazole on the corrosion and corrosion mitigation of cobalt free maraging steel in 0.5 M H2SO4pickling solutions has been reported using electrochemical and spectroscopic investigations. Potentiodynamic polarization data showed that the increase of immersion time from 0 min to 120 min increases the corrosion rate and decreases the polarization resistance of the maraging steel. On the other hand, the addition of PHTA and the increase of its concentration decrease all the corrosion parameters of the steel at all exposure test periods. Electrochemical impedance spectroscopy measurements agreed with the obtained polarization data. Scanning electron spectroscopy and energy dispersive X-ray investigations confirmed that the inhibition of the steel corrosion is achieved via the adsorption of the PHTA molecules onto the steel precluding its surface from being dissolved.

scholarly journals Beneficial Effects of Vanadium Additions on the Corrosion of Ti6AlxV Alloys in Chloride Solutions

Metals ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 264 ◽  
Author(s):  
El-Sayed M. Sherif ◽  
Hany S. Abdo ◽  
Nabeel H. Alharthi
Keyword(s):  
Electron Microscopy ◽  
Immersion Time ◽  
Electrochemical Impedance ◽  
Electrochemical Techniques ◽  
Test Medium ◽  
X Ray ◽  
Beneficial Effects ◽  
Cyclic Potentiodynamic Polarization ◽  
Scanning Electron

The beneficial effects of V addition on the corrosion of a newly manufactured Ti6AlxV (x = 2 wt %, 4 wt %, 6 wt %, and 8 wt %) alloys after various exposure periods in 3.5% NaCl solutions were reported. The Ti6AlxV were produced from their raw powders using mechanical alloying. Several electrochemical techniques such as electrochemical impedance spectroscopy, cyclic potentiodynamic polarization, and potentiodynamic current versus time at 300 mV experiments were conducted. The surface morphology and the elemental analysis were performed using scanning electron microscopy and energy dispersive X-ray analyses. All results were consistent with each other revealing that the increase of V content increases the resistance of the alloys against corrosion. The increase of corrosion resistance was achieved by the role of V in decreasing the rate of corrosion as a result of the formation of oxide films on the surface of the alloys. This effect was found to increase with prolonging the immersion time of the Ti6AlxV alloys in the test medium from 1 h to 24 h and further to 48 h.

scholarly journals Boric Acid as an Accelerator of Cerium Surface Treatment on Aluminum

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
K. Cruz-Hernández ◽  
S. López-Leon ◽  
F. J. Rodríguez-Gómez
Keyword(s):  
Boric Acid ◽  
Polarization Resistance ◽  
Immersion Time ◽  
Surface Characterization ◽  
Electrochemical Impedance ◽  
Electrochemical Techniques ◽  
Industrial Processes ◽  
Aerospace Manufacturing ◽  
Better Than ◽  
Anticorrosion Properties

Aluminum pieces are often used in various industrial processes like automotive and aerospace manufacturing, as well as in ornamental applications, so it is necessary to develop processes to protect these materials, processes that can be industrialized to protect the aluminum as well or better than chromate treatments. The purpose of this research is to evaluate boric acid as an accelerator by optimizing its concentration in cerium conversion coatings (CeCC) with 10-minute immersion time with a concentration of 0.1 g L−1over aluminum to protect it. The evaluation will be carried out by measuring anticorrosion properties with electrochemical techniques (polarization resistance,Rp, polarization curves, PC, and electrochemical impedance spectroscopy, EIS) in NaCl 3.5% wt. aqueous solution and surface characterization with scanning electron microscopy (SEM).

Corrosion and Corrosion Inhibition of Aluminum Alloys A5052 and A5754 in Sulfuric Acid Solutions by Some Inorganic Inhibitors

2017 ◽  
Vol 231 (6) ◽  
Author(s):  
S.S. Abd El-Rehim ◽  
M.A. Deyab ◽  
H.H. Hassan ◽  
Ahamed Abd El-Moneim
Keyword(s):  
Corrosion Resistance ◽  
Sulfuric Acid ◽  
Aluminum Alloys ◽  
Electrochemical Impedance ◽  
Pure Aluminum ◽  
Solution Temperature ◽  
Acid Solutions ◽  
X Ray ◽  
Potentiodynamic Polarization Curves ◽  
Sulfuric Acid Solutions

AbstractThe corrosion of aluminum alloys (A5052 and 5754) in sulfuric acid solutions was investigated using potentiodynamic polarization curves, electrochemical impedance spectroscopy (EIS), scanning electron microscope (SEM), and energy-dispersive X-ray (EDX) methods. For comparison, the corrosion of pure aluminum in sulfuric acid was examined potentiodynamically. The data reveal that increasing sulfuric acid concentrations and solution temperature enhance the corrosion rate of aluminum alloys. The two aluminum alloys exhibit higher corrosion resistance than pure aluminum. Moreover, A5052 involves more corrosion resistance than A5754. The effect of WO

scholarly journals Corrosion Inhibition of Mild Steel by Poly(butylene succinate)-L-histidine Extended with 1,6-diisocynatohexane Polymer Composite in 1 M HCl

2019 ◽  
Vol 2019 ◽  
pp. 1-12 ◽  
Author(s):  
M. G. Tsoeunyane ◽  
M. E. Makhatha ◽  
O. A. Arotiba
Keyword(s):  
Mild Steel ◽  
Corrosion Inhibition ◽  
Polymer Composite ◽  
Electrochemical Impedance ◽  
Condensation Polymerization ◽  
X Ray Diffraction ◽  
Butylene Succinate ◽  
X Ray ◽  
Atomic Force ◽  
Corrosion Inhibition Efficiency

The ecofriendly poly(butylene succinate) extended with 1,6-diisocynatohexane composted with L-histidine (PBSLH) polymer composite was synthesized by condensation polymerization. The polymer composite was characterized by Fourier transform infrared (FTIR), X-ray diffraction (XRD), and scanning electron microscope (SEM-EDX). The inhibition action of the polymer composite was investigated by conventional weight loss, potentiodynamic polarization, variable amplitude micro (VASP), and electrochemical impedance spectroscopy (EIS). The maximum corrosion inhibition efficiency of 78 % was obtained at concentration level of 600 ppm. The results revealed PBSLH as a mixed type corrosion inhibitor. The thermodynamic and kinetic parameters also revealed adsorption of PBSLH on to mild surface as exothermic and the adsorption was conformed to Langmuir model. The morphology of mild steel coupons was investigated by SEM and atomic force microscope (AFM) and the results showed PBSLH to have inhibited corrosion on mild steel in 1 M HCL.

Facile caffeine electrochemical detection via electrodeposited Ag nanoparticles with modifier polymers on carbon paste sensor at aqueous and micellar media

2020 ◽  
Vol 98 (4) ◽  
pp. 169-178 ◽  
Author(s):  
M. Shehata ◽  
S.M. Azab ◽  
A.M. Fekry
Keyword(s):  
Ag Nanoparticles ◽  
Surface Characterization ◽  
Electrochemical Impedance ◽  
Limit Of Detection ◽  
Electrochemical Techniques ◽  
Calibration Plot ◽  
Micellar Media ◽  
Carbon Paste ◽  
Detection Range ◽  
X Ray

The analysis and detection of caffeine (Caf) is very useful due to its widespread usage in several daily consumed beverages, food products, and pharmacological preparations with various physiological effects. The preparation of a newly electrodeposited Ag nanoparticles – cellulose acetate phthalate (CAP) – chitosan (Chit) modified carbon paste (ACCMCP) sensor for sensitive determination of Caf in 0.01 mol L−1 H3PO4 solution (pH 1.0–5.0) both in aqueous and micellar media (0.5 mmol L−1 SDS) was achieved. The interaction of Caf was monitored using electrochemical techniques such as cyclic voltammetry, differential pulse voltammetry, electrochemical impedance spectroscopy, and chronoamperometry, and surface characterization was carried out using X-ray diffraction, scanning electron microscope, and energy dispersive X-ray techniques. The linear detection range of Caf was between 4 and 500 μmol L−1 (r2 = 0.955) and the limit of detection obtained from the calibration plot was 0.252 μmol L−1. The sensor was applicable for detecting Caf in numerous real samples with recoveries from 98.03% to 101.60% without interference of any accompanying species, which ensures high method selectivity.

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