Corrosion Inhibition Of Carbon Steel Research Articles

Protein-derived carbon dots as green corrosion inhibitors for carbon steel in sulfuric acid solution

At present, the development of eco-friendly corrosion inhibitors (CIs) is considered an important and attractive method for controlling the corrosion of metals in acidic media. In this study, protein-derived carbon dots (P-CDs) were prepared via hydrothermal reaction using protein as the raw material, and the corrosion inhibition performances of P-CDs for carbon steel (CS) were investigated systematically. The electrochemical test results showed that the corrosion inhibition efficiency of 500 mg/L P-CDs on CS reached 95.1 % in 0.5 M H2SO4, and the corrosion inhibition efficiency was enhanced to 98.1 % after 8 h of immersion time. The composition and characterization of P-CDs was analysed using Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet Spectroscopy (UV), X-ray Diffraction (XRD) and Transmission Electron Microscopy (TEM). Atomic force microscopy (AFM) and scanning electron microscopy (SEM) characterization showed that the surface of CS with P-CDs was smoother than that without P-CDs, and that P-CDs was able to adsorb on the surface of CS to form a protective layer, thereby inhibiting corrosion. Adsorption studies indicate that P-CDs form a protective layer on the surface of CS through both physisorption and chemisorption. Overall, these findings demonstrate that P-CDs exhibit superior protective effects against the corrosion of CS in 0.5 M H2SO4.

Inhibition of Carbon Steel Corrosion Using Dextran Derivatives in Circulating Cooling Water

Developing environmentally friendly and biodegradable corrosion inhibitors is an important research direction due to the toxicity and non-degradability of conventional carbon steel corrosion inhibitors added to circulating cooling water environments. Polysaccharides in EPSs (Exopolysaccharides) can be used as green corrosion inhibitors, but a low inhibition rate limits their practical application. Chemical modification is widely used to modify the functionality of polysaccharides by altering their physicochemical properties and structures, thereby enhancing or supplementing their functional characteristics. In this study, we employed chloroacetic acid as an esterifying agent to chemically modify Dextran and successfully synthesized a modified polysaccharide derivative with a substitution degree of 0.326. This derivative efficiently inhibited the corrosion of carbon steel in circulating cooling water environments. The carboxymethylated dextran (CM-Dextran) formed after synthesis could adsorb onto metal surfaces to form a protective film, thereby inhibiting metal surface dissolution reactions and exhibiting anodic corrosion inhibition properties. The experimental results showed that the corrosion inhibition efficiency of CM-Dextran after modification increased by up to 57.4%, with a maximum inhibition efficiency of 82.52% at a concentration of 4 mg/mL. This study provides new insights and opportunities for the development of environmentally friendly corrosion inhibitors derived from polysaccharides.

Furosemide drug as a corrosion inhibitor for carbon steel in 1.0 M hydrochloric acid

Furosemide (4-chloro-2-furan-2-ylmethylamino-5-sulfamoylbenzoic acid) was examined as an inhibitor for the corrosion of carbon steel (CS) in 1.0 M HCl. The investigation included mass loss (ML) and electrochemical techniques: potentiodynamic polarization (PP), electrochemical impedance spectroscopy (EIS), and electrochemical frequency modulation (EFM). The efficiency of inhibition rises with increasing Furosemide concentration and temperature. This compound follows the Temkin isotherm with good fit. The presence of varying quantities influences both anodic metal dissolution and cathodic hydrogen evolution. Scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR) were used to detect the effect of the compound on the CS surface. The molecular inhibitory effect of Furosemide was demonstrated using quantum chemical calculations, and the molecular simulation results demonstrated the adsorption on the carbon steel surface.

Green Synthesizing and Corrosion Inhibition Characteristics of Azo Compounds on Carbon Steel under Sweet Conditions: Experimental and Theoretical Approaches.

The deterioration of carbon steel in saline solutions enriched with carbon dioxide represents a significant challenge within the oil and gas industry. So, this study focuses on the design and structural analysis of four azo derivatives: 4-(2-quinolinylazo)-catechol (AZN-1), 4-(4-phenoxyphenylazo)-1-naphthol (AZN-2), 4-(4-pyridylazo)-1-naphthol (AZN-3), and 4-(2-pyridylazo)-1-naphthol (AZN-4), and their first application as effective corrosion inhibitors for carbon steel in a carbon dioxide saturated 3.5% sodium chloride solution. Spectroscopic methods were used to characterize the structural configurations of these compounds. The corrosion protection properties of these compounds on carbon steel in a carbon dioxide saturated 3.5% sodium chloride solution (under sweet conditions) were investigated using Tafel polarization (PDP), electrochemical impedance spectroscopy (EIS), and field emission-scanning electron microscopy (FE-SEM) studies. The results indicate that the inhibition efficiency increases as the concentration of the inhibitors increases. There is a notable agreement between the results obtained from the PDP and EIS measurements, supporting the findings. Moreover, the results displayed that these compounds had significant corrosion protection capabilities at low concentrations, ranging from 91.0 to 98.3% at an additive concentration of 5 × 10-4 M. The PDP profiles showed that these compounds acted as mixed inhibitors, and their adsorption behavior followed the Langmuir isotherm model. Besides, EIS results corroborate the adsorption of AZN compounds through a reduction in double-layer capacitance (Cdl) alongside an augmentation in polarization resistance (Rp) after the addition of AZN compounds into the corrosive solution. Field emission scanning electron microscopy (FE-SEM) and Fourier-transform infrared spectroscopy (FTIR) analysis confirmed the formation of a protective layer on the surface of carbon steel when these inhibitors were applied. In addition, computational calculations and Monte Carlo simulations were performed to support the experimental observations, gain insights into the adsorption properties, and elucidate the corrosion inhibition mechanisms of these compounds.

Corrosion Inhibitors for Carbon Steel in HCl Environment: Synthesis and Characterization of Trimethoprim-Metal Complexes

This study is about making and figuring out what trimethoprim (TM), a popular corrosion inhibitor, is like and then using it as an inhibiting agent to stop corrosion in carbon steel in acid media (HCl solution) through adsorption. TM has also been known as the prevalent anti-corrosive agent. It can be added to a liquid or gas to slow the pace of a chemical reaction (in the case of a material – typically a metal or alloy – that corrodes when it encounters the fluid). Many antibiotic compounds, such as TM derivatives, diiron salt dihydrate, and diiron salt tetrahydrate, have active groups that can stop metal from corroding. Spectroscopic methods like XRD (X-ray difraction), FTIR (Fourier transform infrared spectroscopy), UV-visible (ultraviolet-visible spectroscopy), and TGA (thermogravimetric analysis) were used to study the TM drug. Similarly, the OCP (open circuit voltage) technique was introduced to assess the corrosion resistance and the density of current vs. voltage. Finally, this study revealed that TM drugs could be suggested for introduction as corrosion inhibitors due to their simple production and the fact that they have many active groups that exhibit the ability to coordinate with carbon steel. Our study revealed that changes in inhibitor concentrations, the solution's acidity, and the metal's surface area all contribute to adsorption.

Corrosion Inhibition of Carbon Steel by Some Schiff Base Compounds in HCl and H2SO4 Solutions

AbstractThe inhibition power of two Schiff bases on carbon steel corrosion in 1 M HCl and 0.5 M H2SO4 solutions has been investigated using weight loss, Tafel polarization, and electrochemical impedance spectroscopy techniques. The results revealed that increasing the concentration of inhibitors in acidic solutions led to a higher inhibition efficiency. The polarization curves indicated that the Schiff bases acted as mixed inhibitors, affecting both the cathodic and anodic reactions. The adsorption of the inhibitors on the carbon steel surface followed the Langmuir adsorption isotherm, and various adsorption isotherm parameters such as Kads, ΔGads, ΔHads, and ΔSads were determined at room temperature. Furthermore, the effect of temperature on the inhibitors′ performance was examined within the range of 25–45 °C. The corrosion‐related activation energy, pre‐exponential factor (k), activation enthalpy, and entropy were calculated to assess the inhibitors′ behavior. Scanning electron microscopy (SEM) was employed to examine some carbon steel samples, revealing differences in inhibition efficiency attributed to the inhibitors′ chemical structure. The results highlighted the highest inhibition efficiency in H2SO4 medium at 93.4 %, with a corresponding free energy of 39.51 KJ/mol indicating physical‐chemical adsorption of inhibitor molecules. Furthermore, an enthalpy value of −40.6 KJ/mol suggested an exothermic inhibitor absorption process. The findings are presented and discussed in detail.

Synergistic effect of KI on corrosion inhibition of carbon steel by Styphnolobium japonicum (L.) Schott in H2SO4 solution

This work explored the synergistic effect of Styphnolobium japonicum (L.) Schott extract (SE) and potassium iodide (KI) on the corrosion inhibition of carbon steel (CS) in 0.5 mol/L H2SO4 solution. Firstly, the functional groups in the SE were identified using FTIR. The results of UPLC–Q–TOF–MS analysis confirmed the major phytoconstituents presence in SE were Glutaric acid, 2,3-Dihydroxybenzoic acid, Oxoadipic acid, Isoleucine, 2-Oxovaleric acid, l-phenylalanine, Indoline, and Trigonelline. Further a comprehensive investigation of anticorrosive properties of SE in the absence and presence of KI was conducted employing various techniques, including electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), ultraviolet visible spectroscopy (UV‒vis), and X-ray photoelectron spectroscopy (XPS) and theoretical studies like quantum chemical calculations (QC) and molecular dynamics simulations (MS). The results demonstrated that the SE+KI blend outperforms SE or KI individually, achieving an appreciable corrosion inhibition of 94.6 % for CS in H2SO4 solution. SEM analysis confirmed that the CS surface was smoother when SE+KI was added in the aggressive solution. Theoretical calculations were carried out to determine the dipole moments, Mulliken charges, and Fukui parameters of the eight major molecules found in SE. The results showed that SE can inhibit corrosion.

Synthesis, Characterization, and Electrochemical Study of Novel Porphyrin Derivatives as Corrosion Inhibitors for Carbon Steel in HCl Solutions

This study involves the synthesis of some porphyrins derivatives, these are termed as 4,4',4'',4'''-(porphyrin-5,10,15,20-tetrayl)tetrakis(N-(6-aminoacridin-3-yl)benzamide) (3a), 4,4',4'',4'''-(porphyrin-5,10,15,20-tetrayl)tetrakis(N-(5-methoxybenzo[d]thiazol-2-yl)benzamide) (3b), 4,4'-(10,20-bis(3-hydroxyphenyl)porphyrin-5,15-diyl)bis(N-(6-aminoacridin-3yl)benzamide) (5a), and 4,4'-(10,20-bis(3-hydroxyphenyl)porphyrin-5,15-diyl)bis(N-(benzo[d]thiazol-2-yl)benzamide) (5b). These derivatives were synthesized using open circuit potential (OCP) and potentiodynamic polarization (PDP) in 0.1 M HCl solution methods. These derivatives were characterized using nuclear magnetic resonance (1H- and 13C-NMR) spectroscopy, mass spectra (ESI), and micro elemental analysis (CHN). The activity of these synthesized materials was investigated as a corrosion inhibitor using carbon steel (CS) as a model for corroded materials. The obtained results showed that the synthesized porphyrins derivatives were effective corrosion inhibitors to 0.1 M HCl solution for CS. In the case of the derivative 3a, a maximum inhibition efficiency (IE%) was recorded and it was around 74%. The derivative 3b showed an IE% of around 68.11%, while the %IE of 5a and 5b were around 18.98% and 45.16%, respectively. The best IE% value that was recorded for the derivative 3a has the potential to be effective anticorrosive coatings for industrial applications and act as mixture inhibitor because their ΔEcorr values are less than 85 mV. On the CS surface following treatment with compound 3a, the inhibitor mechanism for acidic medium (HCl) was investigated.

The Possibility of Using Barley Grains Extract as an Acidic Corrosion Inhibitor for Carbon Steel

تمت دراسة تأثير مستخلصات بذور الشعير على تآكل الفولاذ الكربوني في 1M حمض كلور الماء للتحقق من إمكانية استخدام كمثبط أخضر في عملية التنظيف وإزالة الترسبات الحمضية للمبادلات الحرارية، عند درجات حرارة مختلفة. أُجريت عمليات الاستخلاص باستخدام الايثانول والماء %50 حجماً، وبطريقتي النقع والأمواج فوق الصوتية. تمت دراسة آلية تأثير المثبط الذي أعطى أفضل كفاءة تثبيط، من خلال دراسة الامتزاز والتآكل بالطرق الكهروكيميائية (مخططات تافل، ومطيافية المقاومة الكهروكيميائية) والحسابات الترمودينامكية. أظهرت نتائج الدراسة عدم وجود تأثير لطريقة الاستخراج على سلوك التثبيط ، حيث أظهر التثبيط كدالة للتركيز زيادة معنوية في كفاءة التثبيط حتى التركيز 400 جزء في المليون ، ثم ظهرت مستقلة عنها في كلتا الطريقتين. ، ومع ذلك كانت درجة الحماية أعلى لمستخلص طريقة النقع عند التركيز 800ppm 87.01%) مقارنة بـ 80.56% لمستخلص الأمواج فوق الصوتية). أشارت دراسة آلية التثبيط لهذا المستخلص إلى إمكانية الامتزاز الكيميائي للمستخلص وإعادة لترتيب الشحنات في الطبقة المزدوجة الكهربائية . أبدت فعالية التثبيط ارتفاعاً مع درجة الحرارة.

Enhancing steel corrosion resistance in 1.0 M HCl medium through the synthesized and characterized mixed pyrophosphates BMnP2O7 (B = Ni, Co, and Cd)

In this study, we synthesized three diphosphate materials NiMnP2O7, CoMnP2O7, and CdMnP2O7 intended for use as corrosion inhibitors for carbon steel. The crystallinity of the obtained compounds was analyzed using X-ray diffraction (XRD), and a vibrational analysis was carried out by infrared (IR) and Raman (Ra). The corrosion inhibition properties of steel with these materials in 1.0 M HCl solution were investigated using three important techniques. The electrochemical parameters were obtained via electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization curves (PDP) and the surface of the substrate was analyzed, using the scanning electron microscopy (SEM). Our findings indicate that the optimal concentration for NiMnP2O7, CoMnP2O7, and CdMnP2O7 was 10−3 mol/L, with inhibition efficiencies reaching to 87.5 %, 91.04 %, and 92.22 %, respectively. These phosphates also act as a mixed-type inhibitors, imparting high resistance to corrosion, and their inhibition efficiency (η%) increased with the augmentation of the inhibitor concentration. The scanning electron microcopy (SEM) images revealed that the inhibitors form a protective layer against acid attack, preventing carbon steel from being destroyed.

A new Corrosion Inhibitor Based on Modification of Polyacrylic acid in acidic Solution

This search investigates the corrosion inhibition properties of polyacrylic acid. The corrosion inhibition performance of carbon steel (CS) in a 1M HCl solution treated with the polyacrylic acid inhibitor was evaluated using potentiodynamic polarization measurement, Field Emission-Scanning Electron Microscopy (FE-SEM) and Energy Dispersive X-ray Spectroscopy (EDS). The findings of this study demonstrate that polyacrylic acid exhibits significant effectiveness as corrosion inhibitor for CS in Acid solution. The inhibitor acts as a mixed-type inhibitor, and its corrosion inhibition efficiency increases with higher concentrations of polyacrylic Acid concentration up to 89.9% obtained at 298 K for a 400 ppm concentration, while decreasing with increasing acid concentration.

Self‐healing characteristics of superabsorbent polymers in epoxy coating for corrosion inhibition of carbon steels

AbstractThis study evaluated the self‐healing characteristics of superabsorbent polymers (SAP) in epoxy polyamide paint systems applied using brush application. The SAP underwent preliminary characterization to determine its primary properties and was then incorporated into the epoxy primer at different percentages. The epoxy‐SAP coating systems then underwent various tests to evaluate their self‐healing capability. Excellent adhesion is obtained with the coating system composed of initial epoxy primer, epoxy‐SAP layer, final epoxy primer, and an epoxy enamel topcoat. Electrochemical impedance spectroscopy (EIS) reveals that the addition of SAP increased the charge transfer resistance and pore resistance and decreased the double layer capacitance of the coating system in a span of 5 h, confirming the self‐healing of the coating. Maximum corrosion protection for 5 h is obtained between 15 to 20 wt% SAP. Lastly, it is determined through long‐term immersion tests that the addition of SAP in the coating significantly decreases the rust formation; however, the coating starts to peel off due to the swelling of SAP after 2–3 days.

Exploring cinnamon extract’s potential as a green corrosion inhibitor for X65 carbon steel in sulfuric acid: a comprehensive investigation

The effectiveness of cinnamon extract as an environmentally friendly corrosion inhibitor for X65 carbon steel (X65CSt) in a 1 mol/L H2SO4 solution was examined using electrochemical, chemical, and computational techniques. This inhibitor has many advantages, it is safe, environmentally friendly, harmless to human health, and economically feasible. The anticorrosion efficacy rises with rising the concentration of the cinnamon extract and reducing temperature and reaches 95.83% at 450 mg l−1 of cinnamon extract using potentiodynamic polarization. All the investigated methods confirm the anticorrosion ability of cinnamon extract as indicated by the reduced the corrosion current density values and mass loss as well as the greater charge transfer resistance. In addition, the values of the pitting potentials were also transformed in a more noble direction implying the resistance of pitting attack. The polarization technique categorized the cinnamon extract as a mixed inhibitor. The mechanism of inhibition was demonstrated in terms of adsorption of the main components of cinnamon extract onto the surface of X65CSt. of the adsorption of the main components of the cinnamon extract on the surface of the X65CSt and this adsorption is of combined type between both physical and chemical modes, as determined by the computed values of free energy of adsorption, which range between −46.96 and −37.42 kJ. mol−1. The adsorption is exposed to Langmuir isotherm. The four components of cinnamon extract were investigated through density functional theory, Monte Carlo, and Molecular dynamic simulation. The quantum parameters and the adsorption of these components on the Fe(110) reveals that cinnamaldehyde and cinnamic acid inhibitors are more effective as corrosion inhibitors.

Triazole-bearing sulfonamide linkage: Synthesis, characterization, and investigation as a versatile corrosion inhibitor

Novel focused three 1,4-disubstituted-1,2,3-triazoles 5a-c labeled ISMs (ISM-H, ISM-F & ISM-N) and tethering sulfonamide moieties were designed and synthesized by the 1,3-dipolar cycloaddition of some appropriate aromatic O-alkyne derivatives 3a-c and 4-azido-N-carbamimidoylbenzenesulfonamide 4 as an efficient and common approach in click chemistry. The structures of the resulted click products were elucidated based on their spectral data. The newer synthesized triazoles were well investigated as corrosion inhibitors for carbon steel and Al alloy in HCl solution utilizing electrochemical, weight loss, surface research, and density functional theory (DFT) techniques. The electrochemical impedance spectroscopy (EIS) results revealed that a low inhibitor dosage of compounds ISM-H and ISM-F exhibited potential corrosion inhibition. The ISM-N and ISM-H derivatives exhibited a chemisorption nature and showed the potential inhibition at 60 °C. The surface studies: scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX) and Fourier Transform Infrared Spectroscopy (FTIR) reveals the formation inhibitor film above the metal surface.

Insights of 2-(Benzoxazol-2-ylthio)-N-(4-phenyl-5-phenylazo-thiazol-2-yl)-acetamide as a novel corrosion inhibitor for J55 carbon steel in hydrochloric acid: Experimental, Spectroscopic analysis, and theoretical studies

The inhibitory efficacy of 2-(Benzoxazol-2-ylthio)-N-(4-phenyl-5-phenylazo-thiazol-2-yl)-acetamide (BNP) was systematically explored through weight loss measurements, potentiodynamic polarization (PP), and electrochemical impedance spectroscopy (EIS), in relation to the corrosion mitigation of J55 carbon steel (J55CS) within hydrochloric acid (HCl) environments. This research employs a combination of experimental techniques, including gravimetric analysis, electrochemical tests, and theoretical considerations. It has been determined that BNP has an inhibitory effect on the corrosion of J55CS in strong HCl, reaching 91.8% at 18 × 10−6 M at 298 K. The inhibitory efficiency displays a notable enhancement as the concentration of the BNP is elevated within the range of 3–18 × 10−6 M. Conversely, the IE% experiences a raised when the temperature is raised. This augmentation can be attributed to the inherent ability of BNP to facilitate the formation of inhibitory films on the surface of J55CS. An analysis of Tafel plots reveals that the BNP adheres to a mixed-type inhibitor. The adsorption of BNP obeyed the Temkin adsorption isotherm. The investigated isotherm plots revealed that the adsorption process for BNP on the metal surface was endothermic, spontaneous, and chemical adsorption. Theoretical modeling [density functional theory (DFT) and Monte Carlo (MC)] revealed the correlation between the BNP molecular chemical structure and its anticorrosive property.

Corrosion inhibition of carbon steel by eucalyptus leaves in acidic media: An overview

This paper concerns the overview of previous studies on the corrosion and inhibition of carbon steel that is allowed to degrade in a corrosive medium by the extract of the eucalyptus plant, with an emphasis on the extract's adsorption behaviour. Many researchers have largely employed eucalyptus plant bark, oil, and leaf extracts to prevent the corrosion of mild steel in acidic environments under various temperature settings. According to the results, when the bark extract of the eucalyptus plant was added to HCl (5%) at a concentration of 900 ppm, the inhibitor's maximum efficiency was 98.2 %. The leaf extract, on the other hand, had the maximum inhibitory efficacy of 93.09 % at 600 mg/L extract concentration in the H2SO4 (0.5 M) medium. The extracts' potency was shown to diminish with increasing temperature. The mechanism for eucalyptus extract's protection of carbon steel from corrosion in diverse corrosive situations was largely associated with the adsorption of the extract's inhibitive components on the steel's surface to reduce the interaction between the metal and the corrosive surroundings. The majority of the reported inhibitive behaviour of the eucalyptus extract was consistent with the Langmuir adsorption isotherm model.

ρ-Substituted imine cationic surfactants as carbon steel corrosion inhibitors: Experimental and theoretical (DFT and MCs) approaches

In this study, we synthesized cationic surfactants based on ρ-substituted Schiff base compounds—S-12 (E)-N-dodecyl-N,N-dimethyl1-4-((P-olylimino)methy)benzene aminiumchloride) and SO-12 (E)-N-dodecyl-4-(((4-methoxyphenyl)imino)methyl)-N,N-dimethyl benzeneaminiumchloride. Their chemical structures were confirmed via FTIR and 1HNMR spectroscopies. SO-12 decreased the surface tension of 1 M HCl (61 mN.m−1) to 24.4 mN.m−1. Weight loss, electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization (PDP) measurements were employed to investigate carbon steel (CS) corrosion reactions in blank HCl and HCl containing the synthesized surfactants. The CS corrosion suppression actions of S-12 and SO-12 increased with increasing concentrations until they reached approximately 97 %. Adsorption of S-12 and SO-12 delayed the CS corrosion rate. The adsorption process fitted the Langmuir adsorption isotherm. The thermodynamic properties of the CS reaction are also discussed. The surface morphology and elemental analysis of the outer surface layer of CS were studied at the optimal concentration of SO-12 using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). Theoretical results of S-12 and SO-12 agree with experimental data, confirming the effectiveness of S-12 and SO-12 as corrosion inhibitors. Moreover, S-12 and SO-12 have superior performance compared with previously reported cationic surfactants under the same test conditions.

Electrochemical, gravimetric, quantum chemical and computational investigations on an effective synthetic chlorinated cyclic imide derivative as a corrosion inhibitor for carbon steel in sulfuric acid solution

Although many different human activities such as the oil and gas sector, mineral production, utilities, transportation, etc. depend on the utilization of steel and its alloys, they are highly susceptible to corrosion, especially in acidic media. Hence, processing entails substantial material expenditures due to metal losses. In this regard, the inhibitory characteristics of the synthetic heterocyclic derivative (3aR,7S,7aS)-4,5,6,7,8,8-hexachloro-1,3-dioxo-1,3,3a,4,7,7a-hexahydro-2H-4,7-methanoisoindol-2-yl)benzenesulfonamide (MBSI) was studied against corrosion of C-steel in 0.5 M H2SO4 at 25-55 °C. The structure of the synthesized molecule was confirmed by FTIR, 1H-NMR, 13C-NMR, and MS. Weight-loss, potentiodynamic polarization, electrochemical impedance spectroscopy, electrochemical frequency modulation measurements as well as theoretical analyses were employed in this investigation. The results showed that the investigated MBSI compound functions as an efficient inhibitor with a physical adsorption nature on the surface of carbon steel. MBSI concentration causes the inhibition efficiency to rise, reaching a maximum of 94% for the steel alloy corrosion at 37 × 10−6 M and 25°C. The synthesized compound was suggested to act as a mixed-type inhibitor. SEM surface analysis showed the construction of a protective layer at the carbon steel surface. DFT-based quantum chemical indices provided more insight into the inhibitory mechanism. Molecular dynamics (MD) simulations were also applied to predict the conformational adsorption change of the inhibitor on the iron surface. In addition, thermodynamic and kinetic parameters were calculated. The experimental results are largely consistent with the theoretical results.

Justicia brandegeeana as a green corrosion inhibitor for carbon steel in sulfuric acid

ABSTRACT The anti-corrosive effect of the extract in ethanol of Justicia brandegeeana (Acanthaceae) against carbon steel AISI 1020 in sulfuric acid medium 1 mol L−1 was investigated. In addition to the effect of seasonality, several techniques were used to investigate the anti-corrosive activity, such as electrochemical impedance spectroscopy (EIS), potentiodynamic polarization (PP), linear polarization resistance (LPR), and weight loss. The chelating effect was analyzed by UV-Vis spectrophotometry and the surface was analyzed by scanning electron microscopy (SEM). The results showed that the inhibition efficiency is dependent on the concentration of the extract, reaching its maximum at 1500 ppm and despite having good thermal stability (82.41% inhibition at 70°C), it decreases with increasing temperature, indicating a physisorption behavior. The extract obeyed the Langmuir isotherm and the Tafel curves characterized it as a mixed inhibitor, with a tendency to cathodic region. It also presented a 52% chelating effect against Fe+2 ions, and the SEM analysis indicated a protection with the presence of plant extract, thus minimizing surface roughness. These results indicated the J. brangeeana ethanol extract as a green anti-corrosive agent.

Effect of tabebuia heterophylla plant leaves extract on corrosion protection of low carbon steel in 1M HCl medium: Electrochemical, quantum chemical and surface characterization studies.

In the current study the chemical constituents of Tabebuia heterophylla plant leaves extract (THLE) evaluated as corrosion inhibitor for low carbon steel (LCS) in 1 M HCl. The major component present in plant extract was Hexadecanoic acid 2-hydroxy-1-(hydroxymethyl) ethyl ester confirmed by Gas Chromatography with Mass spectroscopic (GC-MS) analysis. Electrochemical impedance spectroscopy (EIS), potentiodynamic polarisation (PDP) and weight loss measurements were used to evaluate the THLE ability to protect low-carbon steel surface against corrosion in 1M HCl medium. The maximum inhibition efficiency reported as 95.45%, 93.99% and 94.79% by weight loss measurements, EIS and PDP methods respectively. In the prolongation of the work, the entropy of adsorption (Δ Sa*), enthalpy of adsorption (Δ Ha*), Gibbs free energy of adsorption (Δ Ga*), and activation energy (Ea) of the reaction were calculated. In absence of inhibitor, the Ea value was found to be minimum 49.38 kJ/mol whereas for optimum concentration of THLE it was found to be 77.2 kJ/mol implies more energy is required to undergo corrosion. The surface morphological observation from Scanning Electron Microscope (SEM), Atomic Force Microscopic (AFM) and Contact angle explored the effective adsorption of THLE. AFM values revealed that average surface roughness (Ra) value of LCS is high (188.08), where as in the presence of THLE, Ra values significantly reduced to minimum value of 37.226. Further chemical interactions between THLE and the low-carbon steel surface as well as inhibitory mechanism were further elucidated by theoretical simulations such as Density Functional Theory (DFT) calculations and Molecular dynamics (MD) simulations.