scholarly journals Corrosion behaviour of copper in wet bentonite Rokle B75

2014 ◽  
Vol 58 (2) ◽  
pp. 43-47 ◽  
Author(s):  
J. Stoulil ◽  
L. Horáčková ◽  
J. Říhová-Ambrožová

Abstract Materials for storing nuclear waste are a hot topic all over the globe right now. This study monitors corrosion behaviour of copper as one of the contemplated materials in the Czech bentonite Rokle B75. The tests were carried out in a thermostated cell deaerated with argon at temperatures of 90 and 40°C in the environment of bentonite pore solution, bentonite pore solution with an addition of sulphides and wet bentonite suspension. The scanning electron microscopy, X-ray diffraction, Raman spectroscopy, electrochemical impedance spectroscopy and resistometric methods of corrosion rate measurements were applied. The most compact layer is formed in the environment of bentonite pore solution. The addition of sulphides leads to a significant growth of thickness of the layer of corrosion products and its porosity. However, the porosity decreases towards the layer - metal interface. The layer formed after exposure to the wet bentonite suspension is reported to have the worst parameters. Nevertheless, considering the final temperature of 40°C in the repository, the corrosion rate will still be acceptable.

2017 ◽  
Vol 35 (1) ◽  
pp. 35-46 ◽  
Author(s):  
Zhiping Zhu ◽  
Xiandi Zuo ◽  
Zhaohui Ying

AbstractThe power supply accident caused by the corrosion of metal materials in the substation has become an important issue that affects the safe operation of the power grid. The corrosion of copper T2 was the most serious. The corrosion behaviour of copper T2 in SO2- and H2S-containing atmospheric environments was investigated using electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), energy-dispersive X-ray spectrometry (EDS), and X-ray diffraction (XRD), and the nonequidistant grey GM(1,1) model was established of which the precision and forecast dependability were evaluated. Results indicated that the corrosion rate of copper in the SO2 environment increased in the early stages of corrosion and then gradually decreased at the later stages. In contrast, the corrosion rate of copper in the H2S environment slowly increased in the early stages of corrosion and then sharply increased at the later stages. The corrosion products in the SO2 environment consisted of cuprite (Cu2O) and brochantite [Cu4(OH)6SO4], whereas the corrosion products in the H2S environment were Cu2O and chalcocite (Cu2S). The mathematical model has good prediction dependability and higher forecast reliability.


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.


2019 ◽  
Vol 63 (1) ◽  
pp. 19-22
Author(s):  
J. Stoulil ◽  
M. Kouřil ◽  
D. Dobrev

Abstract The goal of the study was to compare corrosion performance of copper in different bentonite slurries. Copper coil samples were exposed in a slurries of bentonites BaM, Rokle, B75, G2M, Voltex, Sabenil. The test was carried out under anaerobic conditions in glovebox at laboratory temperature for duration of one to four months. Samples were evaluated by means of X-ray diffraction and mass loss. Liquid parts of slurries were analysed by ion chromatography and pH meter. The resistance of copper in all studied bentonites was very high. Corrosion rates were in order of tenths of micrometers per year. No trend between pore solution composition and corrosion rate or composition of corrosion products was observed.


2009 ◽  
Vol 289-292 ◽  
pp. 469-476
Author(s):  
J. Nieto ◽  
M.P. Hierro ◽  
F.J. Bolívar ◽  
F.J. Pérez

The influence of Al and Al-Si coatings on the corrosion behaviour of HCM12 in molten KCl-ZnCl2 mixture at 650°C in air has been characterized by electrochemical impedance spectroscopy (EIS). Al and Al/Si protective coatings were developed by chemical vapour deposition in fluidized bed reactor (CVD-FBR) at moderate temperature to respect to mechanical properties of substrate. Scanning electron microscopy (SEM) was used to analyse the damage on the HCM12 electrode surface. Al-Si coating was found to be more resistant to the molten chlorides attack than Al coating; and both coatings increased the corrosion resistance of HCM12 in these conditions. The surface composition has been determined by X-ray diffraction (XRD).


2017 ◽  
Vol 729 ◽  
pp. 40-45 ◽  
Author(s):  
Wei Bing Kong ◽  
Xin Xin Li ◽  
Xin Ping Hu

AlMg5Si1-xRE (x=0%, 0.9%) alloys were prepared by resistance melting method, and the phases of alloy were analyzed by X-ray diffraction (XRD) and scanning electron microscope (SEM). The effects of RE (rare earth) on the corrosion resistance of AlMg5Si1 alloy immersed in seawater in different time were investigated by potential measurements and electrochemical impedance spectroscopy. The results showed that the strengthening phase β (Mg2Si) was short rod like and dispersing distributed in α (Al) in the AlMg5Si1 alloy after adding 0.9% RE. Under the conditions of seawater immersion, the corrosion rate of the AlMg5Si1RE0.9 alloy was less than that of AlMg5Si1 alloy, and the corrosion rate of AlMg5Si1RE0.9 immersed 12h in seawater was the slowest, 5.7 uA·cm-2. The improved corrosion resistance is due to the changes in microstructure and corrosion products.


Scanning ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-8
Author(s):  
Yanbing Tang ◽  
Xinwang Shen ◽  
Zhihong Liu ◽  
Ying Li

A comprehensive corrosion investigation of pure Fe in an environment of solid sodium salt deposit (i.e., NaCl or Na2SO4) with mixtures of H2O and O2 at 500°C was conducted by mass gain measurement, X-ray diffraction (XRD), scanning electron microscope (SEM), potentiodynamic polarization, and electrochemical impedance spectroscopy (EIS). The results showed that corrosion rates were accelerated with solid NaCl or Na2SO4 deposit due to their reaction with the formed protective scale of Fe2O3 and subsequently resulted in its breakdown. The corrosion rate of pure Fe with solid NaCl is higher than that with solid Na2SO4 because of the lower activation energy (Ea) for chemical reaction of Fe in solid NaCl+H2O+O2 (i.e., 140.5 kJ/mol) than that in solid Na2SO4+H2O+O2 (i.e., 200.9 kJ/mol). Notably, the electrochemical corrosion rate of pure Fe with solid NaCl deposit, 1.16×10−4 A/cm2, was a little lower than that with solid Na2SO4 deposit.


Coatings ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 712
Author(s):  
Channagiri Mohankumar Praveen Kumar ◽  
Avinash Lakshmikanthan ◽  
Manjunath Patel Gowdru Chandrashekarappa ◽  
Danil Yurievich Pimenov ◽  
Khaled Giasin

Zinc (Zn) is one of the five most widely consumed metals in the world. Indeed, more than 50% of all the zinc produced is used in zinc-galvanizing processes to protect steel from corrosion. Zn-based coatings have the potential for use as a corrosion-resistant barrier, but their wider use is restricted due to the poor mechanical properties of Zn that are needed to protect steel and other metals from rusting. The addition of other alloying elements such as Ni (Nickle) and WC (Tungsten Carbide) to Zn coating can improve its performance. This study investigates, the corrosion performance of Zn–Ni coating and Zn–Ni–WC composite nanocoatings fabricated on mild steel substrate in an environmentally friendly bath solution. The influence of WC nanoparticles on Zn–Ni deposition was also investigated. The surface morphologies, texture coefficients via XRD (X-ray diffraction), SEM (Scanning Electron Microscopy), and EDS (Energy-dispersive X-ray spectroscopy) were analyzed. The electrochemical test such as polarization curves (PC) and electrochemical impedance spectroscopy (EIS) resulted in a corrosion rate of 0.6948 Å/min for Zn–Ni–WC composite nanocoating, and 1.192 Å/min for Zn–Ni coating. The results showed that the Zn–Ni–WC composite nanocoating reduced the corrosion rate by 41.71% and showed an 8.56% increase in microhardness compared to the hardness of the Zn–Ni coating. These results are augmented to better wettable characteristics of zinc, which developed good interfacial metallurgical adhesion amongst the Ni and WC elements. The results of the novel Zn–Ni–WC nanocomposite coatings achieved a great improvement of mechanical property and corrosion protection to the steel substrate surface.


Author(s):  
Hayette Faid

AbstractIn this work, Zn-Ni alloys have been deposited on steel from sulfate bath, by electrodeposition method. The effect of Zn content on deposits properties was studied by cyclic voltammetry (CV), chronoaperometry (CA), linear stripping voltammetry (ALSV) and diffraction (XRD) and scanning electronic microscopy (SEM). The corrosion behavior in 3.5 wt. NaCl solution was examined using anodic polarization test and electrochemical impedance spectroscopy. X-ray diffraction of show that Zn-Ni alloys structure is composed of δ phase and γ phase, which increase with the decrease of Zn content in deposits. Results show that deposits obtained from bath less Zn2+ concentration exhibited better corrosion resistance.


2020 ◽  
Vol 38 (4A) ◽  
pp. 491-500
Author(s):  
Abeer F. Al-Attar ◽  
Saad B. H. Farid ◽  
Fadhil A. Hashim

In this work, Yttria (Y2O3) was successfully doped into tetragonal 3mol% yttria stabilized Zirconia (3YSZ) by high energy-mechanical milling to synthesize 8mol% yttria stabilized Zirconia (8YSZ) used as an electrolyte for high temperature solid oxide fuel cells (HT-SOFC). This work aims to evaluate the densification and ionic conductivity of the sintered electrolytes at 1650°C. The bulk density was measured according to ASTM C373-17. The powder morphology and the microstructure of the sintered electrolytes were analyzed via Field Emission Scanning Electron Microscopy (FESEM). The chemical analysis was obtained with Energy-dispersive X-ray spectroscopy (EDS). Also, X-ray diffraction (XRD) was used to obtain structural information of the starting materials and the sintered electrolytes. The ionic conductivity was obtained through electrochemical impedance spectroscopy (EIS) in the air as a function of temperatures at a frequency range of 100(mHz)-100(kHz). It is found that the 3YSZ has a higher density than the 8YSZ. The impedance analysis showed that the ionic conductivity of the prepared 8YSZ at 800°C is0.906 (S.cm) and it was 0.214(S.cm) of the 3YSZ. Besides, 8YSZ has a lower activation energy 0.774(eV) than that of the 3YSZ 0.901(eV). Thus, the prepared 8YSZ can be nominated as an electrolyte for the HT-SOFC.


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.


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