Corrosion Inhibition Of Steel Research Articles

Millettia aboensis leaves extract as eco-friendly corrosion inhibitor for mild steel in acidizing solution: From experimental to molecular level prediction

The development of environmentally friendly corrosion inhibitors is becoming more popular since conventional inhibitors are poisonous and non-biodegradable. The anti-corrosive effectiveness of Millettia aboensis leaves extract (MALE) has been assessed in this study using several methods, such as electrochemical measurements, X-ray Photoelectron spectroscopy and scanning electron microscopy on mild steel in acidic solution. Gas chromatography-mass spectrometry (GC-MS) analysis was combined with qualitative and quantitative phytochemical analysis to identify the phytochemicals linked to the activity of the Millettia aboensis extracts and identified key phytoconstituents such as Hexanedioic acid, Phenol derivatives, Octadecanoic acid, and Linolenic acid, which play significant roles in the extract's inhibitory performance. The results showed that the inhibition efficiency (IE%) improved to 88.6 % with the addition of inhibitor concentration from 0.1 g/L to 3.0 g/L and that the corrosion rate drastically reduced from 56.91 mpy to 16.09 mpy. Furthermore, at a greater concentration (3.0 g/L), the Rct values rose from 61.42 Ω cm2 to 176.3 Ω cm2 thus, indicating that the inhibitor molecules were forming a protective film over the metallic surface. Scanning Electron Microscopy (SEM) provided visual evidence of surface morphology, revealing a smoother surface in the presence of the inhibitor, indicative of the protective film formed by the adsorption of organic molecules onto the steel surface. Theoretical calculations using the ωB97XD functional and def2svp basis set further supported the experimental findings, showing that the protonated form of C21H36O4 exhibited the highest interaction energy, correlating with its superior inhibition efficiency on the metal surface.

Microbial corrosion inhibition of mild steel by Bacillus thuringiensis

Microbial corrosion inhibition of mild steel by Bacillus thuringiensis

Synthesis of new binary trimethoxyphenylfuran pyrimidinones as proficient and sustainable corrosion inhibitors for carbon steel in acidic medium: experimental, surface morphology analysis, and theoretical studies

In this study, synthesis and assessment of the corrosion inhibition of four new binary heterocyclic pyrimidinones on CS in 1.0 M hydrochloric acid solutions at various temperatures (30–50 °C) were investigated. The synthesized molecules were designed and synthesized through Suzuki coupling reaction, the products were identified as 5-((5-(3,4,5-trimethoxyphenyl)furan-2-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-trione (HM-1221), 2-thioxo-5-((5-(3,4,5-trimethoxyphenyl)furan-2-yl)methylene)dihydropyrimidine-4,6(1H,5H)-dione (HM-1222), 1,3-diethyl-2-thioxo-5-((5-(3,4,5-trimethoxyphenyl)furan-2-yl)methylene)dihydropyrimidine-4,6(1H,5H)-dione (HM-1223) and 1,3-dimethyl-5-((5-(3,4,5-trimethoxyphenyl)furan-2-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-trione (HM-1224). The experiments include weight loss measurements (WL), electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization (PDP). From the measurements, it can be shown that the inhibition efficiency (η) of these organic derivatives increases with increasing the doses of inhibitors. The highest η recorded from EIS technique were 89.3%, 90.0%, 92.9% and 89.7% at a concentration of 11 × 10−6 M and 298 K for HM-1221, HM-1222, HM-1223, and HM-1224, respectively. The adsorption of the considered derivatives fit to the Langmuir adsorption isotherm. Since the ΔGoads values were found to be between − 20.1 and − 26.1 kJ mol−1, the analyzed isotherm plots demonstrated that the adsorption process for these derivatives on CS surface is a mixed-type inhibitors. Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), atomic force microscope (AFM) and Fourier- transform infrared spectroscopy (FTIR) were utilized to study the surface morphology, whereby, quantum chemical analysis can support the mechanism of inhibition. DFT data and experimental findings were found in consistent agreement.Graphical

Exploration of modified β-cyclodextrin compounds as enhanced eco-friendly and easily accessible corrosion inhibitors for carbon steel in hydrochloric acid

β-CD was esterified independently with two distinct ionic liquids to evaluate their potential as corrosion inhibitors for carbon steel in a 1.0 M HCl solution. Experimental and computational methods were used to assess the inhibitors’ efficiency regarding temperature and concentration effects and to elucidate the adsorption mechanism. Both inhibitors acted as barriers, with a maximum inhibition efficiency of about 94 % at 200 ppm. There was a direct relationship between the inhibitor's concentration and their efficiency, while increasing the temperature reduced the inhibitors’ effectiveness. The thermodynamic and kinetic parameters were evaluated and studied. DFT calculation revealed the electronic structure and reactivity of the inhibitors. Molecular dynamic simulation provided insight into the optimal configuration and binding energies of inhibitors on the Fe (110) surface.

The corrosion inhibition performance of a diissocyanate-imidazole based organic compound during acid cleaning of MSF desalination plant

Inorganic scale formation is a common issue in multi-stage flash (MSF) desalination plants, significantly impacting operational efficiency. To address this, acid cleaning is frequently employed, but it can lead to severe corrosion of alloy components if not properly controlled with corrosion inhibitors. This study investigates the effectiveness of toluene-2,4-diisocyanate-4-(1H-imidazole-ly) aniline (TDIA) as a corrosion inhibitor for 304L stainless steel in a simulated acid cleaning solution (1M HCl and 3.5 % NaCl). A range of tests, including electrochemical analysis, weight loss measurements, and surface characterization techniques such as AFM, EDS, and SEM, were used to assess the inhibitor's performance at temperatures of 25, 45, 65, and 90 °C. At a concentration of 50 ppm, TDIA achieved inhibition efficiencies of around 90% at 25 °C and above 80% at 90 °C, demonstrating effective protection across all temperatures studied. The adsorption behavior of TDIA followed the Langmuir adsorption model, and it acted as a mixed-type inhibitor by forming a protective layer on the metal surface, which prevents corrosive agents from accessing the steel. The dual-environment testing method, simulating conditions in desalination plants, offers valuable insights into the inhibitor's practical performance, enhancing the applicability of these findings to real-world industrial scenarios.

Corrosion Inhibition of Carbon Steel in Neutral Chloride Solutions Using Salts of Primary Bile Acids.

Due to growing environmental concerns and regulatory pressures, the demand for environmentally friendly corrosion inhibitors has increased. Biosurfactants are biodegradable and have a low toxicity. However, very few studies have reported on their potential use as corrosion inhibitors. The present study reports the novel application of two bile salts (sodium cholate NaC and sodium chenodeoxycholate NaCDC) as environmentally friendly corrosion inhibitors for carbon steel in a neutral 20 mM NaCl solution. The results of potentiodynamic polarization and electrochemical impedance measurements showed that when added at a concentration of 5 mM, the corrosion inhibition efficiencies of NaC and NaCDC were about 60% and 85%, respectively. The poor inhibitory character of NaC was confirmed by XPS analysis, revealing the formation of oxidative corrosion products on the steel surface. For the steel sample immersed in the solution containing NaCDC, the XPS measurements showed clear evidence of the presence of an organic layer and a passive oxide film on the steel surface. While the steroidal skeleton of NaC is characterized by marked biplanarity (considering its hydrophobic and hydrophilic faces), NaCDC features a steroidal ring with a hydrophilic edge (it does not exhibit biplanarity). Thus, the self-assembly and adsorption behavior of these bile salts on the steel surface are different, leading in the case of NaCDC to form a densely packed protective organic layer.

Trifolium repens extracts as a green corrosion inhibitor for carbon steel in a 3.5% NaCl solution

BackgroundMaterial degradation is a major issue that has been the subject of intense research and investigation by the scientific community. It has harmful consequences that require serious and careful intervention. However, restrictions on the use of inhibitors containing toxic compounds pose a significant challenge to the implementation of effective corrosion treatments. This has necessitated a continuous search for new and innovative ways to protect against material damage. Plant-derived natural inhibitors offer several advantages, including potent inhibitory effects, lack of toxicity, biodegradability, and environmentally sustainable origins. The purpose of this research was to evaluate the corrosion resistance of API5LX60 carbon steel in a 3.5 % NaCl environment using Trifolium repens as an environmentally friendly inhibitor. MethodsThe inhibitor extract was analysed using Fourier Transform Infrared (FTIR) spectroscopy. However, gravimetry and electrochemical methods (potentiodynamic polarization and electrochemical impedance spectroscopy (EIS)) were used to investigate the corrosion behaviour. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used to examine the surface morphology. Significant findingsAfter testing a range of concentrations in a 3.5 % NaCl medium, the highest level of inhibition (98 %) was obtained at 20 ppm, confirming the mixed action of the inhibitor with predominantly cathodic action. The inhibition mechanism involved physical adsorption on metal surfaces according to the Langmuir model, which enhances the corrosion-inhibiting ability; the extract forms a protective layer that successfully inhibits corrosion, as confirmed through electrochemical and surface analysis. These results demonstrate that the extract acts as a potent anticorrosive agent.

Correction: Current Trend Review in the Application of Pyridine-Based Molecule as Robust Steel Corrosion Inhibitors

Correction: Current Trend Review in the Application of Pyridine-Based Molecule as Robust Steel Corrosion Inhibitors

A study on the corrosion inhibition impact of newly synthesized quinazoline derivatives on mild steel in 1.0 M HCl: Experimental, surface morphological (SEM-EDS and FTIR) and computational analysis

Two new quinazoline derivatives were investigated in this research, namely 12-(4-methoxyphenyl) and 3,3-dimethyl-12-(4-nitrophenyl)-3,4,5,12-tetrahydrobenzo[4,5]imidazo[2, 1-b]quinazolin-1(2 H)-one (Q-NO2). In 1 M hydrochloric acid (HCl), −3,3-dimethyl-3,4,5,12-tetrahydrobenzo[4,5]imidazo[2,1-b]quinazolin-1(2 H)-one (Q-OMe) proved to be an extremely effective corrosion inhibitor for mild steel. The maximum inhibition efficiencies of 94.7 % for Q-NO2 and 96.7 % for Q-OMe were achieved when the performance of the inhibitors was evaluated using potentiodynamic polarization (PDP), electrochemical frequency modulation (EFM) and electrochemical impedance spectroscopy (EIS). According to these findings, the Q-NO2 and Q-OMe molecules have a remarkable ability to generate a dense, resistant protective film on the mild steel surface. This protective film acted as a barrier, effectively blocking the penetration of corrosive ions and their interaction with the mild steel substrate. The adsorption characteristics of these inhibitors on the mild steel surface conform to the Langmuir adsorption isotherm. PDP experiments show that Q-NO2 and Q-OMe act as mixed-type inhibitors for mild steel in 1.0 M HCl. Surface characterization by energy dispersive X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM) determined that a protective layer had formed on the steel surface, preventing corrosion. The experimental results were corroborated by theoretical insights from density functional theory (DFT), which further clarified the molecular adsorption processes. This work highlights the potential of Q-NO2 and Q-OMe as effective inhibitors to protect mild steel in acidic situation.

A comprehensive electrochemical evaluation of the corrosion inhibition by sodium silicate on carbon steel

Sodium silicate (SS) is investigated as a sustainable green corrosion inhibitor for carbon steel in saline environment under both static and dynamic flow conditions. Potentiodynamic scans and Electrochemical Impedance Spectroscopy revealed that silica is both highly efficient in static and flowing water conditions (up to 98 and 99% resp.). An increased inhibition efficiency (IE) is seen as a function of silica concentration as a result of decreased defects in the resulting silica film (Mott–Schottky). The film forming behaviour changes at increasing flow speed, producing a more defect-rich structure at both low and high silica concentration, although showing improved IE at intermediate flow speed for low SS concentrations.

Experimental study on corrosion inhibition of mild steel using Mukia maderaspatana leaves extract as green inhibitor

In this work, investigations were conducted into the adsorption behaviour and inhibitory effect of Mukia maderaspatana leaves extract on the corrosion of mild steel in 1.5M HCl solution at several temperatures. The techniques included chemical methods (weight loss measurements), surface analysis (SEM, FESEM) and solution analysis (UV–visible spectrophotometric, ICP-MS) techniques. The examination of the data revealed that the efficiency of inhibition rose as the inhibitor's concentration increased and fell as the temperature increased. At 30 degrees Celsius, the concentration of inhibitor resulted in an increase in corrosion inhibition efficiency, reaching 99.02% efficiency at 8% concentration. The physical adsorption of the inhibitor on the metal surface was demonstrated by the adsorption free energy of the plant extract on mild steel. The conclusions above are supported by data from examinations of Scanning Electron Microscopy, FESEM, UV–visible and Fourier transform infrared spectrophotometry.

Theoretical study of novel antipyrine derivatives as promising corrosion inhibitors for mild steel in an acidic environment

Theoretical study of novel antipyrine derivatives as promising corrosion inhibitors for mild steel in an acidic environment

An electrochemical and theoretical approach towards the efficient microwave synthesis of imidazolium-based ionic liquids for unprecedented mild steel corrosion inhibition in 0.5 M H2SO4 solution

The inhibition potential of newly synthesized imidazolium-based ionic liquids (IL-1 and IL-2) on mild steel corrosion in a 0.5 M H2SO4 solution has been comprehensively investigated using gravimetric analysis, potentiodynamic polarization, and electrochemical impedance spectroscopy across various temperatures. Gravimetric analysis indicated that the adsorption of these inhibitors adhered to the Langmuir adsorption isotherm. Significantly, IL-2, featuring a longer alkyl chain, demonstrated superior inhibition efficiency (92.51 % at 303 K) compared to IL-1 (88.71 % at 303 K). Potentiodynamic polarization studies revealed a mixed-type inhibitory behavior, impacting both anodic and cathodic reactions. Surface morphological analyses via SEM and EDX confirmed the formation of a protective film on the mild steel surfaces, substantiating the corrosion inhibition capabilities of IL-1 and IL-2. The novelty of this research lies in the application of density functional theory (DFT) using the B3LYP method, which elucidated that the alkyl chain length at the N-3 position in imidazolium cation-based ionic liquids significantly enhances their inhibition potential. This mechanistic insight suggests that these ionic liquids effectively obstruct both anodic and cathodic sites, providing robust corrosion protection in a 0.5 M H2SO4 solution.

Eco-friendly modified chitosan as corrosion inhibitor for carbon steel in acidic medium: Experimental and in-depth theoretical approaches

The industrial and medical sectors have a great interest in chitosan due to its unique properties, such as abundance, renewability, non-toxicity, antibacterial activity, biodegradability, and polyfunctionality. In this work, two modified chitosan Schiff bases (ChSB-1 and ChSB-2) were made using condensation methods, and their potential as corrosion inhibitor for carbon steel in 1 M HCl was investigated using chemical and electrochemical techniques. The ChSB-1 and ChSB-2 inhibitors exhibited remarkable inhibitory performance, as evidenced by the mass loss data, which showed 89.3 % and 91.5 % efficacy at 1 mM concentration, respectively. Because of the electron-donor substituent of methoxy (–OCH3), ChSB-2's active sites have more delocalized electrons than ChSB-1's. The PDP results showed that both ChSB-1 and ChSB-2 inhibitors have anti-corrosion characteristics because heteroatoms caused a protective layer to develop that functioned as mixed-typed inhibitors. The calculated adsorption-free energy ∆Gadso for ChSB-1 and ChSB-2, respectively, was found −36.1 and − 37.1 kJ mol−1. The ChSB-1 and ChSB-2 inhibitors adsorb on carbon steel in acidic conditions through physisorption and chemisorption interactions, and their adsorption is in line with the Langmuir adsorption model. Inhibited and uninhibited metallic surfaces were subjected to surface morphological assessments using contact angle (CA), the scanning electron microscopy and the energy dispersive X-ray (SEM/EDX) analysis. The DMol3 part of Materials Studio 7.0 software was used to perform the quantum chemical calculations based on DFT to visualize the structural features. Studies from quantum chemistry suggest the possibility of surface interaction between the unoccupied orbitals of the metal surface and the inhibitors ChSB-1, ChSB-2, ChSB-1H+, and ChSB-2H+. The results clearly show that the two inhibitors work well as environmentally friendly carbon steel corrosion inhibitors in acidic medium. This could be advantageous for industrial procedures such as pickling, cleaning, acidizing oil drilling in oil wells, and using citrus to de-sediment boilers.

Electrochemical, thermodynamic and DFT studies of Fomitopsis pinicola as green corrosion inhibitor for carbon steel in sulfuric acid

In this work, the methanolic extract of Fomitopsis pinicola has been evaluated as a green corrosion inhibitor for the dissolution of 1018 carbon steel in 0.5 M sulfuric acid. For this, gravimetric tests and electrochemical methods such as potentiodynamic polarization curves, linear polarization resistance (LPR) and Electrochemical Impedance Spectroscopy (EIS) techniques were used. These tests were aided with Infrared and GC–MS analytical techniques. In addition to this, theoretical calculation with the use of the density functional theory (DFT) technique has been used to correlate the electronic extract properties and its inhibitory capacity. Weight loss results have shown an inhibitor efficiency of 85 % with the addition of 400 ppm. Thermodynamic parameters have shown that Fomitopsis pinicola extract is physically adsorbed onto the steel following a Langmuir adsorption isotherm. Potentiodynamic polarization curves showed that the extract behaves as a mixed type of corrosion inhibitor inducing the formation of a protective film onto the steel surface. In the presence of the Fomitopsis pinicola extract, a more resistive film obtained the highest polarization resistance value when 400 ppm of extract was used. In addition to this, as the concentration of the extract increased the charge transfer resistance and the double electrochemical layer capacitance decreased. GC–MS results indicated that main compounds contained in the Fomitopsis pinicola extract were Dehydrergosterol, Hydrazino-acetic acid ethyl ester, and Phthalic acid, di (2-propylpentyl) ester, whereas theoretical calculations showed that the highest EHOMO and lowest ELUMO values correspond to Dehydrergosterol and the Phthalic acid, which are the responsible for the extract inhibitory properties.

New Benzimidazole derivatives as efficient organic inhibitors of mild steel corrosion in hydrochloric acid medium: Electrochemical, SEM/EDX, MC, and DFT studies

The corrosion of mild steel (MS), a widely used material in industry, represents a significant global challenge. In order to extend the durability of equipment, the use of corrosion inhibitors proves to be an effective solution, particularly in corrosive environments. In this research, two newly synthesized benzimidazole derivatives, namely 1-(cyclohex-1-en-1-yl)-3-[(3-phenyl-1,2-oxazol-5-yl)methyl]-2,3-dihydro-1H-1,3-benzodiazol-2-one (Benz1) and 1-(cyclohex-1-en-1-yl)-3-[(3-phenyl-4, 5-dihydro-1,2-oxazol-5-yl)methyl]-2,3-dihydro-1H-1,3-benzodiazol-2-one (Benz2), were evaluated as corrosion inhibitors for MS in 1 M hydrochloric acid solution. This study was conducted using both experimental methods and computational approaches. Potentiodynamic polarization diagrams (PDP) indicate that, depending on concentration effects, Benz1 and 2 function as mixed-type inhibitors, with a predominance of cathodic inhibition. The results of electrochemical impedance spectroscopy (EIS) show that the compounds tested offer high inhibition efficiencies of 96.32 % and 98.30 % at 10−⁴ M for Benz1 and 2, respectively. Inhibitor adsorption follows the Langmuir isotherm and involves chemisorption. SEM/EDX analyses confirm the presence of a protective film on the metal. In addition, DFT and Monte Carlo simulations reveal significant adsorption of the compounds on the MS surface, underlining their high potential as effective corrosion inhibitors.

Electrochemical and computational evaluation of hydrazide derivative for mild steel corrosion inhibition and anticancer study

In the present study the authors’ main goal is to avoid the corrosive attack of the chloride ions of 3.5% NaCl solution in saline medium on the mild steel (MS), by addition of small amount of a new derivative of the hydrazide called ligand (HL), as a corrosion inhibitor. This study had been achieved by employing different electrochemical measurements such as, open circuit potential (OCP), electrochemical impedance spectroscopy (EIS) and potentio-dynamic polarization (PDP) methods. The results of the electrochemical test (OCP), showed that, the open circuit potential of the mild steel in saline solution, was guided to more positive direction in presence of the ligand (HL), at its ideal concentration (1 × 10−3 M), compared to the (OCP), of the mild steel in absence of (HL). The results of the electrochemical methods, EIS and PDP presented that, the ligand (HL), was acted as a good corrosion inhibitor for hindering the corrosion process of the mild steel in 3.5% sodium chloride, as it was recorded a good percentage of the inhibition efficiency (77.45%, 53.41%, by EIS and PDP techniques respectively), at its optimum concentration (1 × 10−3 M). Also, the corrosion rate of the mild steel in the saline medium without (HL), was listed about (0.0017 mm/year), while in existence of (HL), was decreased to a value about (0.00061 mm/year). As well, some of electrical properties of (HL), and its derivative [Pd(II), Cr(III), and Ru(III)], complexes were investigated such as; the activation energy (Ea(ac)), which recorded values in the range of 0.02–0.44 (eV) range and electrical conductivity which listed values at room temperature in the range of 10−5–10−8 S.cm−1. The results of the AC and DC electrical conductivity measurements for (HL), and its derivative [Pd(II), Cr(III) and Ru(III)] complexes indicate semiconducting nature which suggests that these compounds could be used in electronic devices. Also, the complexes exhibited higher conductivity values than (HL). Photophysical studies showed good florescence properties of HL that indicated that it can be used to determine most of the drugs with no fluorescence properties by quenching and calculating quantum yield. Moreover, the hydrazide ligand (HL), has shown selectivity as an active anticancer candidate drug for both breast and colon cancer in humans. Density function theory demonstrated that, the frontier molecular orbital HOMOs of the complexes have exhibited similar behavior and the charge density has localized in the metallic region of all the studied complexes. Also, the values of the energy gap of the ligand (HL), and its complexes Pd(II), Cr(III) and Ru(III), had been arranged in this order HL > Cr(III) > Ru(III) > Pd(II). All characterization using different spectroscopic techniques were reported to elucidate the proposed structures such as; thermal analysis, elemental analysis of C, H, and N atoms, spectral analysis using IR, UV, 1H NMR techniques, scanning electron microscopy and energy dispersive X-ray analyses.

Assessment of Warionia saharea Essential Oil as a Green Corrosion Inhibitor for Mild Steel in HCl: Experimental and Computational Studies

The objective of this research work is the study of the inhibitory effect of Warionia saharea essential oil (WSEO) on the corrosion of mild steel (MS) in molar HCl solution, employing both experimental and theoretical methods. This inhibitory effect (IE) has been evaluated by using a combination of weight loss measurements (LW) and various electrochemical methods, such as open circuit potential (OCP), potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) experiments. The LW results indicated that IE increased with inhibitor concentration, reaching 83.34% at 3.00 g/L. The PDP analysis suggested that WSEO functions as a mixed inhibitor, while in the EIS results the Rct values increased with inhibitor concentration to reach 165.8 Ω cm2 at 2.00 g/L, suggesting a defensive film formation by WSEO molecules over the metallic surface. The thermodynamic study demonstrated that the WSEO molecules adsorption on the MS surface followed a Langmuir isotherm, involving mixed physical and chemical (physicochemical) adsorption on the MS surface. Theoretical methods, including density functional theory (DFT) and molecular dynamics (MD) simulations, were employed to elucidate the inhibition mechanisms of the three main components of WSEO. The quantum chemical analysis, using density functional theory (DFT) and molecular dynamics (MD) simulations, showed a low ΔEgap value of 6.30 eV and a low adsorption energy (Eads) value on an Fe (110) substrate of −258 Kcal/mol for (E)-Nerolidol, indicating the significant contribution of this molecule to the overall corrosion inhibition effect of WSEO. The scanning electron microscope (SEM) analysis verified the presence of a protective film formed by the inhibitor on the MS surface. This study highlights the potential of WSEO as a sustainable and green corrosion inhibitor in acidic environments.

Chitosan grafted with gallic acid and cerium dioxide hybrid nanocomposites as environmentally friendly corrosion inhibitors for mild steel: An experimental and computational study

Chitosan grafted with gallic acid (CS-GA), along with CS-GA doped with CeO2 nanoparticles (CS-GA-CeO2) were synthesized as novel environmentally friendly mild steel corrosion inhibitors. The formation of these derivatives was confirmed by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), hydrogen nuclear magnetic resonance spectroscopy (1H NMR), and thermal analysis (TGA). Based on potentiodynamic polarization curves (PDP) measurements, the inhibitors acted primarily as hybrid inhibitors, while following the Langmuir adsorption theory model. Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy(XPS) and 3D surface profiles, confirmed that CS-GA-CeO2 adsorbed on the mild steel forming a protective layer thus preventing the invasion of corrosive media. The corrosion protection mechanism of chitosan derivatives was investigated by molecular dynamics simulations. Electrochemical measurements were used to investigate the corrosion inhibition by CS-GA and CS-GA-CeO2 on mild steel in a 3.5 % NaCl solution. At room temperature, the highest inhibition efficiency (93.58 %) was achieved at 200 ppm CS-GA-CeO2. Modified chitosan nanocomposites were confirmed as promising corrosion inhibitors.

Insight into the Anti-Corrosion Mechanism of Halogen Anions in Bisimidazoline Derivatives as Corrosion Inhibitor for Q235 Steel in 1.0 mol/L HCl

Insight into the Anti-Corrosion Mechanism of Halogen Anions in Bisimidazoline Derivatives as Corrosion Inhibitor for Q235 Steel in 1.0 mol/L HCl