scholarly journals Galvanic Corrosion of SA106 Gr.B Coupled with Magnetite in Alkaline Solution at Various Temperatures

Materials ◽  
2019 ◽  
Vol 12 (4) ◽  
pp. 628
Author(s):  
Soon-Hyeok Jeon ◽  
Geun Song ◽  
Sang Kim ◽  
Do Hur

The effect of temperature on the galvanic corrosion behavior of SA106 Gr.B carbon-manganese steel was studied in an alkaline aqueous solution at various temperatures (30, 60, and 90 °C) via electrochemical corrosion tests. At all temperatures studied, carbon-manganese steel acted as the anode of the galvanic cell composed of carbon-manganese steel and magnetite because the corrosion potential of carbon-manganese steel was significantly lower than that of magnetite. The corrosion current density of carbon-manganese steel significantly increased due to the galvanic effect irrespective of temperature used in this study. With the increase in temperature, the extent of the galvanic effect on the corrosion current density of carbon-manganese steel and reductive dissolution of magnetite gradually increased. When the area ratio of magnetite to carbon-manganese steel increased, the corrosion rate of the carbon-manganese steel in contact with magnetite further increased.

2020 ◽  
Vol 9 (1) ◽  
pp. 496-502 ◽  
Author(s):  
Zhaohui Zhang ◽  
Bailong Liu ◽  
Mei Wu ◽  
Longxin Sun

AbstractThe electrochemical behavior of gold dissolution in the Cu2+–NH3–S2O32−–EDTA solution has been investigated in detail by deriving and analyzing the Tafel polarization curve, as this method is currently widely implemented for the electrode corrosion analysis. The dissolution rate of gold in Cu2+–NH3–S2O32−–EDTA solution was determined based on the Tafel polarization curves, and the effects of various compound compositions in a Cu2+–NH3–S2O32−–EDTA mixture on the corrosion potential and corrosion current density were analyzed. The results showed that the corrosion potential and polarization resistance decreased, whereas the corrosion current density increased for certain concentrations of S2O32−–NH3–Cu2+ and EDTA, indicating that the dissolution rate of gold had changed. The reason for promoting the dissolution of gold is also discussed.


2010 ◽  
Vol 663-665 ◽  
pp. 473-476
Author(s):  
Shu Qi Zheng ◽  
Chang Feng Chen ◽  
Rui Jing Jiang ◽  
Dan Ni Wang

In the environment with H2S/CO2 or Na2S, the corrosion behavior of Lanthanum hexaboride (LaB6) was investigated by electrochemistry methods. The results indicated that the corrosion potential (Ecorr) and Rf of LaB6 increased as the partial pressure of H2S increased, while the corrosion current density (Icorr) decreased. In the environment containing Na2S, as the content of Na2S increased, the corrosion potential (Ecorr) and Rf of LaB6 decreased, while the corrosion current density (Icorr) increased. Thus, the addition of H2S into the environment with H2S/CO2 would inhibit the corrosion of LaB6; while in the environment containing Na2S, the increasing of the content of Na2S would accelerate the corrosion of LaB6.


2013 ◽  
Vol 756-759 ◽  
pp. 85-88
Author(s):  
Xiao Ming Wang ◽  
Sheng Zhu ◽  
Qing Chang ◽  
Guo Feng Han

Al-based coating on ZM5 magnesium alloy was prepared by Supersonic Particles Deposition (SPD). Electrochemical working station was utilized to test polarization curve, corrosion potential and electrochemical impedance spectroscopy etc. The results indicted that corrosion potential of Al-Si coating was about-767.6mV, much higher than that of ZM5 Mg-substrate; And corrosion current density of the coating sample decreased three order of magnitude than that of the uncoated. Compared to Mg-substrate, the radius of capacitive impedance arc of the coating enlarged and impedance modulus improved two order of magnitude.


2011 ◽  
Vol 243-249 ◽  
pp. 5562-5566
Author(s):  
Jin Liang Lu ◽  
Jun Xi Zhang ◽  
Jun Jiang ◽  
Kun Wang ◽  
Wen Jun Qu

In this paper, the feasibility of inhibitor auxiliary re-alkalization was investigated. The effect of realkalization auxiliary inhibitor repair technique was studied by simulative experiment. It studied the changes of electrochemical parameters of the natural carbonated reinforced concrete during the electrochemical realkalization in 1mol/L Na2CO3 solution and the mixed solution of 1mol/L Na2CO3 and 1 mol/L DMEA , as well as the impedance spectroscopy and polarization curves in the process of relaxation. The results showed that: there appears to be no effect of DMEA on the corrosion potential and the impedance of the steel in the process of realkalization. That was, the performance was the same as that in the sodium carbonate solution except corrosion current of rebar with DMEA which showed much lower. But of the samples which the DMEA existed in the electrolyte was significantly shorter at the same relaxation time after realkalization. At the same relaxation time the corrosion potential was more positive and the corrosion current density was smaller. It improved significantly the effect of realkalization.


2014 ◽  
Vol 1033-1034 ◽  
pp. 829-833 ◽  
Author(s):  
Xiao Fei Yao ◽  
Wei Tian ◽  
Ling Wu

Electrochemical methods were employed to investigate galvanic corrosion behaviors of super13Cr and P110 couples in NaCl solution at different temperature. Corrosion morphologies and products of the couples were analyzed by SEM, EDS and XRD. The results showed that there were potential difference distinctly between super 13Cr and P110 steel in NaCl solution at different temperature, when its contacted, galvanic corrosion of super 13Cr-P110 steel couples will occurred. P110 was accelerated to corrode as anode and super 13Cr was protected as cathode in the coupling. Super 13Cr-P110 steel couples could not be used as P110 without any protection in NaCl solution at 20 °C to 80 °C. Corrosion current density and galvanic corrosion of super13Cr-P110 steel couples increased with increasing temperature in NaCl solution, of which corrosion products are Fe3O4.


2019 ◽  
Vol 26 (3) ◽  
pp. 219-225
Author(s):  
Robert Starosta

Abstract Due to the paramagnetic properties and the ability to passivation, for the production of hulls of some vessels (mainly warships), corrosion-resistant (stainless) steels with austenitic structure are used. This article describes the influence of seawater salinity on selected corrosion properties of high-alloy steel X5CrNi 18-10 (304). The average salinity of the seas is taken as 3.5% content of sodium chloride. Corrosion rate of the tested material was evaluated in an aqueous solution of sodium chloride was evaluated. The NaCl concentration in corrosive solutions was 0.7%, 1.4%, 2.1%, 2.8%, 3.5%, 4.2%. Corrosion tests were performed using the potentiodynamic method. The range of electrochemical potential changes was Ecorr ±150 mV. Corrosion rate was assessed on the basis of corrosion current density measurements. Corrosion potential values against the saturated calomel electrode were also determined. Based on the obtained measurement results and non-parametric significance tests carried out, a significant influence of seawater salinity on the value of corrosion current density and corrosion potential was found. The highest value of corrosion current density (jcorr), and thus the highest corrosion rate, was recorded for 3.5% NaCl solution. In the concentration range from 0.7 to 3.5% NaCl in solution, the corrosion rate of austenitic steel increases. A further increase in salinity of electrolyte results in the inhibition of corrosion rate of steel. There is almost a full negative, linear correlation between the proportion of sodium chloride in the corrosive solution and the value of corrosion potential. Along with the rise in the salinity of seawater, increase the electrochemical activity, and thus the corrosion susceptibility, thus the corrosion susceptibility, of the austenitic steel X5CrNi 18-10 was observed.


2020 ◽  
Vol 10 (3) ◽  
pp. 1089 ◽  
Author(s):  
Wioletta Raczkiewicz ◽  
Artur Wójcicki

The electrochemical galvanostatic pulse method (GPM) is used for the evaluation of the degree of corrosion risk of reinforcement in concrete. This non-destructive method enables determining the corrosion promoting conditions through the measurements of reinforcement stationary potential and concrete cover resistivity, and determining the probability of reinforcement corrosion in the tested areas. This method also allows for the estimation of the reinforcement corrosion activity and the prediction of the development of the corrosion process on the basis of corrosion current density measurements. The ambient temperature (and the temperature of the examined element) can significantly affect the values of the measured parameters due to electrochemical character of the processes as well as specific measurement technique. Differences in the obtained results can lead to a wrong interpretation of reinforcement corrosion risk degree in concrete. The article attempts to assess the effect of temperature on the measured parameters while using the galvanostatic pulse method. The GP-5000 GalvaPulseTM set was used. The results of this study confirmed the impact of temperature changes on the values of three measured parameters (reinforcement stationary potential, concrete cover resistivity, and corrosion current density) and contributed to catching the trend of these changes.


2019 ◽  
Vol 66 (6) ◽  
pp. 704-718
Author(s):  
Qingmiao Ding ◽  
Zili Li ◽  
Tao Shen ◽  
Gan Cui

Purpose This paper aims to research the corrosion behavior of the metal under the disbonded coatings interfered with AC through electrochemical method. Design/methodology/approach The corrosion behavior of the metal under disbond coating interfered with alternate stray current (AC) was studied by electrochemical methods using the rectangular coating disbonded simulator. The obtained data from electrode potential test, electrochemical impedance spectroscopy (EIS) and polarization curves in simulated soil solution indicated that under the natural corrosion condition, the self-corrosion potential and the corrosion current density of the metal at different depths under disbond coating had obviously changed if there was AC interference. Findings The self-corrosion potential of the metal at the same depths under disbond coating shifted negatively with the rising of the AC voltage. Under the condition of cathode polarization, there was still obvious potential gradient with the extension of the deep peeling of the coating gap, and the corrosion current density of the test points was minimum, and the protection effect was best when the cathode protection potential was −1.0 V. When the metal was applied with over-protection, the corrosion rate of the metal increased as AC stray current flowing through it increased. Originality/value This paper used the rectangular aperture device to study the corrosion behavior of X80 steel under the disbonded coatings through electrochemical methods when the AC stray current interference voltage was 0V, 1V, 5V or 10V and the protection potential was 0V, −0.9V, −1.0V, −1.2V or −1.3V, respectively. There is great significance to the safe operation and long-term service of pipeline steel in soil environment.


2017 ◽  
Vol 2017 ◽  
pp. 1-13 ◽  
Author(s):  
Qingmiao Ding ◽  
Liping Fang ◽  
Yanyu Cui ◽  
Yujun Wang

A rectangle disbonded coating simulation device was used to research the effect of sulfate reducing bacteria (SRB) on the metallic corrosion behavior under disbonded coating by the electrochemical method. The results showed that the metal self-corrosion potential at the same test point had little change in the initial experiment stage, whether the solution was without or with SRB. The potential amplitude in the solution with SRB was larger than that without SRB in the later corrosion period. The corrosion current density of the metal at the same test point increased gradually over time in the solution with or without SRB, and SRB could accelerate the corrosion of the metal in the disbonded crevice. The metal self-corrosion potential in the crevice had little change in the SRB solution environment after adding the fungicide, but the corrosion current density decreased significantly. That meant the growth and reproduction of SRB were inhibited after adding the fungicide, so the metal corrosion rate slowed down. Among the three kinds of solution environment, increasing the coating disbonded thickness could accelerate the corrosion of the metal in the crevice, and it was the largest in the solution with SRB.


Materials ◽  
2021 ◽  
Vol 14 (20) ◽  
pp. 6130
Author(s):  
Johannes H. Potgieter ◽  
David Whitefield ◽  
Vivian Motsumi

Electrochemical polarisation tests were carried out on three grades of WC-Co cemented carbides to investigate the corrosive behaviour of the hardmetals and rank them as viable protective liners for chutes and skips in the mining industry. The cobalt binder content and WC particle size varied. The binder content ranged from 6–12 wt%, and the grain size of the WC particles ranged from 0.4–2.3 µm. The performance of the WC-Co hardmetal was compared to three different grades of high chromium white cast irons and Hadfield steel. The cast irons varied in both their chromium content and the morphology of the Cr-rich primary carbides. Potentiodynamic polarisation and linear polarization resistance scans were used to determine the corrosion current density and other electrochemical parameters. The microstructural characteristics of the samples were analysed using Scanning Electron Microscope(SEM) with Energy Dispersive Spectroscopy (EDS), and optical microscopy. The potentiodynamic scans revealed that, although the WC-Co alloys were found to have generally improved corrosion resistance, it was the high-Cr white cast iron (22 wt% Cr) that recorded the lowest corrosion current density and therefore displayed the best resistance against corrosive attack in 1 M H2SO4. The Hadfield steel exhibited the poorest resistance to corrosion and therefore, suffered the most degradation to its exposed surface.


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