scholarly journals Imidazolium-Based Ionic Liquid as Efficient Corrosion Inhibitor for AA 6061 Alloy in HCl Solution

Materials ◽  
2020 ◽  
Vol 13 (20) ◽  
pp. 4672
Author(s):  
Xiaohong Wang ◽  
Ailing Huang ◽  
Dongquan Lin ◽  
Mohd Talha ◽  
Hao Liu ◽  
...  

The corrosion inhibition performance of an imidazolium-based ionic liquid (IL), 1-butyl-3-methylimidazolium thiocyanate (BMIm), was studied on AA 6061 alloy in 1 M HCl solution at 303 K, 333 K, and 363 K by gravimetric tests, potentiodynamic polarization, and electrochemical impedance spectroscopy (EIS) analysis. Scanning electron microscopy with energy dispersive X-ray (SEM-EDX) and X-ray photoelectron spectroscopy (XPS) were used to detect the surface morphologies and chemical composition of the surface films. The results indicate that this IL inhibits AA 6061 corrosion in acid with maximum inhibition efficiencies of 98.2%, 86.6%, and 41.2% obtained at 303 K, 333 K, and 363 K respectively. Inhibition efficiency generally decreased with increasing immersion time; the major exception was at 303 K, whereby the inhibition efficiency was detected to increase with immersion time from 30 to 90 min and then decrease slightly beyond 90 min. The results indicate that BMIm is a mixed-type inhibitor with a predominant effect on cathodic reactions. Surface morphology analyses by SEM revealed less surface damage in the presence of the inhibitor. XPS analysis established the development of a protective film on the AA 6061 surface which was hydrophobic in nature.

2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
R. Ganapathi Sundaram ◽  
M. Sundaravadivelu

An anticorrosion activity of 8-quinoline sulphonyl chloride (8-QSC) on mild steel in 1 M HCl solution was studied by weight loss (WL) method and electrochemical methods, namely, electrochemical impedance spectroscopy (EIS), Tafel polarization (TP), and linear polarization resistance (LPR). Results obtained from WL method, EIS, TP, and LPR, showed that 8-QSC is a good corrosion inhibitor for mild steel in 1 M HCl solution. The results indicated that the inhibition efficiency and extent of surface coverage were increased with increase in inhibitor concentration and decrease in the corrosion rate. This is due to the formation of protective film on the surface of mild steel. Adsorption of 8-QSC on the mild steel surface was found to obey the Langmuir adsorption isotherm. A Tafel plot indicates that the used inhibitor behaves predominantly as cathodic type. The surface morphology of the mild steel was studied by Scanning Electron Microscopy (SEM) and Energy Dispersive X-Ray (EDX) Spectroscopy techniques. All the methods give the same order of inhibition efficiencies.


Nanomaterials ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 535 ◽  
Author(s):  
María-Dolores Avilés ◽  
Ramón Pamies ◽  
José Sanes ◽  
María-Dolores Bermúdez

Graphene (0.5 wt.%) was dispersed in the hydrophobic room-temperature ionic liquid 1-octyl-3-methylimidazolium bis(trifluoromethanesulfonyl) imide (IL) to obtain a new non-Newtonian (IL + G) nanolubricant. Thin layers of IL and (IL + G) lubricants were deposited on stainless steel disks by spin coating. The tribological performance of the new thin layers was compared with those of full fluid lubricants. Friction coefficients for neat IL were independent of lubricant film thickness. In contrast, for (IL + G) the reduction of film thickness not only afforded 40% reduction of the friction coefficient, but also prevented wear and surface damage. Results of surface profilometry, scanning and transmission electron microscopy (SEM and TEM), energy dispersive analysis (EDX), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy were discussed.


2019 ◽  
Vol 9 (2) ◽  
pp. 99-111
Author(s):  
Wejdene Mastouri ◽  
Luc Pichon ◽  
Serguei Martemianov ◽  
Thierry Paillat ◽  
Anthony Thomas

Stainless steels are broadly used thanks to their specific physical properties such as their high corrosion resistance in poorly aggressive solutions. However, only few studies have been reported in the literature concerning their electrochemical behavior in low concentration electrolytes medium. Accordingly, the present work aims to study the immersion time influence on the solid-liquid interface properties of the austenitic stainless steel AISI 304L, immersed in a low-concentrated (0.01 M) sodium chloride (NaCl) solution. The electroche­mical behavior of the interface was evaluated by electrochemical impedance spectroscopy (EIS) and open circuit potential (OCP) monitoring. The morphological features and the modification of the surface composition were evaluated by Optic Microscopy, Scanning Electron Microscopy, Energy Dispersive X-ray Spectrometry, Atomic Force Microscopy, White Light Interferometry and X-ray Photoelectron Spectroscopy. It was determined by OCP measurement that the characteristic time of the interface stabilization is very long (several months). After an immersion of 2 months in NaCl solution, a second time constant on impedance phase diagram appears. Surface characterizations reveal a significant modifi­cation of the morphology and chemistry of the AISI 304L surface that can be linked to OCP/EIS observations. It can be noticed that the repeatability deviation of the EIS method was about 1 % while its reproducibility deviation was estimated to 35 %.


2008 ◽  
Vol 47-50 ◽  
pp. 1466-1469 ◽  
Author(s):  
Dong Jin Kim ◽  
Hyuk Chul Kwon ◽  
Seong Sik Hwang ◽  
Hong Pyo Kim ◽  
Jang Yul Park

Corrosion-resistant nickel-based Alloy 600 is susceptible to a lead-induced stress corrosion cracking (PbSCC) in aqueous solutions. The lead species incorporated into the oxide at the alloy surface degraded the passivity, and caused the PbSCC. Effects of lead on the properties of the surface passive films were investigated. The cross sections of the surface films were examined by the transmission electron microscopy and the species present in the films were analyzed with the energy dispersive x-ray spectroscopy and the x-ray photoelectron spectroscopy. In-depth concentration profiles of the species were analyzed by using an ion sputtering technique. The electrochemical impedance spectroscopy technique was used to characterize the electrochemical behaviors. Effectiveness of a nickel boride inhibitor was evaluated. The boride inhibitor altered the properties of the passive film, and significantly reduced the susceptibility to the PbSCC.


Coatings ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 106
Author(s):  
Akbar Ali Samsath Begum ◽  
Raja Mohamed Abdul Vahith ◽  
Vijay Kotra ◽  
Mohammed Rafi Shaik ◽  
Abdelatty Abdelgawad ◽  
...  

In the present study, the corrosion inhibition effect of Spilanthes acmella aqueous leaves extract (SA-LE) on mild steel was investigated in 1.0 M HCl solution at different temperature using weight loss, Tafel polarization, linear polarization resistance (LPR), and electrochemical impedance (EIS) measurements. Adsorption of inhibitor on the surface of the mild steel obeyed both Langmuir and Temkin adsorption isotherms. The thermodynamic and kinetic parameters were also calculated to determine the mechanism of corrosion inhibition. The inhibition efficiency was found to increase with an increase in the inhibitor concentration i.e., Spilanthes acmella aqueous leaves extract, however, the inhibition efficiency decreased with an increase in the temperature. The phytochemical constituents with functional groups including electronegative hetero atoms such as N, O, and S in the extract adsorbed on the metal surface are found responsible for the effective performance of the inhibitor, which was confirmed by Fourier-transform infrared spectroscopy (FT-IR) and ultraviolet–visible spectroscopic (UV-Vis) studies. Protective film formation against corrosion was confirmed by scanning electron microscopy (SEM), atomic force microscopy (AFM), and contact angle studies. The result shows that the leaves extract acts as corrosion inhibitor and is able to promote surface protection by blocking active sites on the metal.


Author(s):  
Ke Qu ◽  
Yuqi Bai ◽  
Miao Deng

Abstract The ever-increasing need for small and lightweight power sources for use in portable or wearable electronic devices has spurred the development of supercapacitors as a promising energy storage and conversion system. In this work, a simple, facile and easy-to-practice method has been developed to employ carbon paper (CP) as the support to coat molybdenum disulfide (MoS2) and graphene oxide (GO), followed by electrodeposition of polyaniline (PANI) to render CP/MoS2-GO-PANI. The preparation parameters, such as amounts of MoS2, GO and number of aniline electropolymerization cycles, have been optimized to render CP/MoS2-GO-PANI the best capacitive performance. The as-prepared optimal CP/MoS2-GO-PANI is characterized by X-ray powder diffraction, scanning electron microscopy, energy-dispersive spectroscopy, and X-ray photoelectron spectroscopy. The supercapacitive properties of CP/MoS2-GO-PANI as an electrode have been evaluated electrochemically via cyclic voltammetry, galvanostatic charge/discharge, and electrochemical impedance spectroscopy testing. CP/MoS2-GO-PANI delivers a specific capacitance of 255.1 F/g at 1.0 A/g and exhibits excellent rate capability under larger current densities. Moreover, a symmetrical supercapacitor is assembled and three are connected in series to power a light-emitting diode for ~15 minutes, demonstrating the promising application potential of CP/MoS2-GO-PANI-based supercapacitor.


2016 ◽  
Vol 6 (6) ◽  
pp. 20160056 ◽  
Author(s):  
R. Pruna ◽  
F. Palacio ◽  
M. Martínez ◽  
O. Blázquez ◽  
S. Hernández ◽  
...  

Fabrication and organosilane-functionalization and characterization of nanostructured ITO electrodes are reported. Nanostructured ITO electrodes were obtained by electron beam evaporation, and a subsequent annealing treatment was selectively performed to modify their crystalline state. An increase in geometrical surface area in comparison with thin-film electrodes area was observed by atomic force microscopy, implying higher electroactive surface area for nanostructured ITO electrodes and thus higher detection levels. To investigate the increase in detectability, chemical organosilane-functionalization of nanostructured ITO electrodes was performed. The formation of 3-glycidoxypropyltrimethoxysilane (GOPTS) layers was detected by X-ray photoelectron spectroscopy. As an indirect method to confirm the presence of organosilane molecules on the ITO substrates, cyclic voltammetry and electrochemical impedance spectroscopy (EIS) were also carried out. Cyclic voltammograms of functionalized ITO electrodes presented lower reduction-oxidation peak currents compared with non-functionalized ITO electrodes. These results demonstrate the presence of the epoxysilane coating on the ITO surface. EIS showed that organosilane-functionalized electrodes present higher polarization resistance, acting as an electronic barrier for the electron transfer between the conductive solution and the ITO electrode. The results of these electrochemical measurements, together with the significant difference in the X-ray spectra between bare ITO and organosilane-functionalized ITO substrates, may point to a new exploitable oxide-based nanostructured material for biosensing applications. As a first step towards sensing, rapid functionalization of such substrates and their application to electrochemical analysis is tested in this work. Interestingly, oxide-based materials are highly integrable with the silicon chip technology, which would permit the easy adaptation of such sensors into lab-on-a-chip configurations, providing benefits such as reduced size and weight to facilitate on-chip integration, and leading to low-cost mass production of microanalysis systems.


Author(s):  
Muddasir Nawaz ◽  
Sehrish Habib ◽  
Adnan Khan ◽  
Abdul Shakoor ◽  
Ramazan Kahraman

The use of organic coating for the metals has been widely being used to protect the surface against corrosion. Polymeric coating incorporated with Nanocontainers loaded with inhibitor and self-healing provides better corrosion resistance. Cellulose microfibers (CMFs) used as smart carriers were synthesized and loaded with dodecylamine (DOC)-inhibitor and polyethyleneimine (PEI)-both inhibitor and self-healing agents. Smart polymeric coatings were developed by mixing CMF/DOC and CMFs/PEI into the epoxy matrix. Reference coatings (that has only CMFs) were also prepared for a compersion. Scanning electron microscope (SEM), X-ray diffraction spectroscopy (XRD), Fourier transform infrared spectroscopy (FTIR) and thermal gravitational analysis (TGA) were used to confirm the loading of DOC and PEI onto the CMFs. UV-vis analysis indicates that the self-release of inhibitor from CMFs is sensitive to pH of the solution and the immersion time. Recovery of controlled surface damage confirms the decent self-healing ability of the prepared smart coatings is due to the efficient release of inhibitor (DOC) and self-healing agent (PEI) in the damaged area leading to the formation of a protective film. Electrochemical impedance spectroscopy (EIS) results demonstrate that corrosion resistance of the smart coating increases with an increase in immersion time which is due to the progressive release of inhibitors from CMFs in response to the pH change. Therefore, smart coatings demonstrate superior properties as compared to the reference coatings. The study reveals the polymeric composite coatings have potential to inhibit the corrosion of steel for oil and gas industry.


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