Synthesis and Inhibition Effect of a Novel Tri-cationic Surfactant on Carbon Steel Corrosion in 0.5 M H2SO4 Solution

A novel Tri-cationic surfactant was synthesized, purified and characterized. The critical micelle concentration value of the prepared surfactant was determined by surface tension and conductivity measurements. The surface parameters were calculated by surface tension measurements. The relationship between the surface properties and the corrosion inhibition efficiency of the prepared surfactant was discussed. The inhibition effect of the novel Tri-cationic surfactant on carbon steel corrosion in 0.5 M H₂SO₄ was studied by potentiodynamic polarization, electrochemical impedance spectroscopy and weight loss techniques. Potentiodynamic polarization studies revealed that the inhibitor acted as a mixed-type inhibitor. The high inhibition efficiency was attributed to the blocking of active sites on the steel surface through the adsorption of inhibitor molecules. Inhibitor adsorption on the carbon steel surface was in accordance with the Langmuir adsorption isotherm model. Thermodynamic adsorption and kinetic parameters were obtained from weight losses at different temperatures (20–60 °C).     

A Corrosion Inhibition Study of a Novel Synthesized Gemini Nonionic Surfactant for Carbon Steel in 1 M HCl Solution

In this study, a gemini nonionic surfactant was synthesized as a corrosion inhibitor for carbon steel in 1 M HCl. Surface properties of the synthesized gemini nonionic surfactant were determined by using surface tension. The results showed that the gemini nonionic surfactant has good surface active properties. The corrosion inhibition effect of the synthesized inhibitor on carbon steel was evaluated by using electrochemical impedance spectroscopy (EIS), potentiodynamic polarization and weight loss methods. The characterization of the film formed on the steel surface was carried out by scanning electron microscope (SEM) methods. The inhibitor molecules were adsorbed physically onto a carbon steel surface according to the Langmuir adsorption isotherm. The results revealed that the inhibitor acted as a mixed-type inhibitor. It was found that the inhibition efficiency increases with an increase in inhibitor concentration and decreases with increasing temperature. Thermodynamic parameters were calculated to elucidate the inhibitive mechanism.     

THE ROLE OF PHOSPHONATE DERIVATIVES ON THE CORROSION INHIBITION OF STEEL IN HCL MEDIA

The inhibition of corrosion of steel by two P-containing compounds, sodium methyldodecyl phosphonate and sodium methyl (11-smethacryloyloxyundecyl) phosphonate, in hydrochloric acid has been investigated at various temperatures using electrochemical techniques (impedance spectroscopy (EIS), potentiodynamic polarization) and weight loss measurements. Inhibition efficiency (E%) increased with phosphonate concentration. Adsorption of inhibitors on the steel surface in 1 M HCl follows the Langmuir isotherm model. EIS measurements showed that the dissolution process of steel occurred under activation control. Polarization curves indicated that inhibitors tested acted as cathodic inhibitors. The temperature effect on the corrosion behavior of steel in 1 M HCl without and with the inhibitor was studied in the temperature range from 313 to 353 K. The adsorption free energy and activation parameters for the steel dissolution reaction in the presence of phosphonates were determined.     

The Oil from Mentha rotundifolia as Green Inhibitor of Carbon Steel Corrosion in Hydrochloric Acid

The corrosion inhibition potentials of Mentha rotundifolia oil on carbon steel in 1 M HCl was studied at different concentrations via gravimetric, electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques. Polarization curves reveal that Mentha rotundifolia oil is a mixed-type inhibitor. Changes in impedance parameters (charge transfer resistance R_t, and double-layer capacitance C_dl) were indicative of adsorption of Mentha rotundifolia on the metal surface, leading to the formation of a protective film. The effect of the temperature on the corrosion behavior with addition of the optimal concentration of Mentha rotundifolia oil was studied in the temperature range 308 and 338 K. Adsorption of oil on the carbon steel surface is found to obey the Langmuir adsorption isotherm. Attempts to explain the inhibitory action were carried out using density functional theory (DFT) at B3LYP/6-31G(d,p) level. Quantum chemical parameters most relevant to its potential action as corrosion inhibitor such as E_HOMO (highest occupied molecular orbital energy), E_LUMO (lowest unoccupied molecular orbital energy), energy gap (ΔE), and Mulliken charges have been calculated and discussed. The theoretical results were found to be consistent with the experimental data.     

A study of hydroxyethyl imidazoline as H2S corrosion inhibitor using electrochemical noise and electrochemical impedance spectroscopy

A study of H₂S corrosion inhibition of pipeline steel by hydroxyethyl imidazoline has been carried out by using electrochemical techniques. Inhibitor concentration included 5, 10, 25, 50, and 100 ppm in a H₂S-containing 3% NaCl solution at 50 °C. Techniques included linear polarization resistance (LPR), electrochemical impedance spectroscopy (EIS), and electrochemical noise (EN) measurements. In addition to the traditional noise in voltage and current, noise resistance (R _n) measurements were used. All techniques showed that the most efficient inhibitor concentration was between 5 and 10 ppm, but inhibitor efficiency decreased after 8 h of testing. Furthermore, EN measurements showed that steel was highly susceptible to localized corrosion at inhibitor doses lower than 10 ppm due to the establishment of a porous inhibitor film. However, with 50 or 100 ppm of inhibitor, the steel was susceptible to a mixture of uniform and localized corrosion. Hurst exponent was higher in presence of inhibitor for times shorter than 8 h, indicating a short residence time of the inhibitor. The data could not be fitted to any adsorption isotherm model, indicating a lack of strong adsorption of the inhibitor to the metal surface.     

Luffa aegyptiaca leaves extract as corrosion inhibitor for mild steel in hydrochloric acid medium

The performance of methanol extract of Luffa aegyptiaca leaves (MLA) as corrosion inhibitor for mild steel (MS) in 1 M HCl was investigated by potentiodynamic polarization and electrochemical impedance spectroscopy. Polarization measurements showed that the MLA acts as a mixed inhibitor. It was found that the percentage inhibition efficiency increased with MLA concentration and decreased with temperature. Thermodynamic parameters indicate the spontaneous adsorption of MLA on MS surface. In addition, it has been established that the adsorption process obeyed Langmuir isotherm. Additions of halide ions considerably increase the inhibition efficiency. Synergistic parameters confirm the synergistic effect of halide ions. The adsorption of the chemical constituents of MLA on MS surface was confirmed by Fourier transform infrared spectroscopy and atomic force microscopy.     

Synergistic corrosion inhibition effect of 1-ethyl-1-methylpyrrolidinium tetrafluoroborate and iodide ions for low carbon steel in HCl solution

Investigation into the corrosion inhibition of low carbon steel in 0.1-M HCl solution by 1-ethyl-1-methylpyrrolidinium (EMTFB) and the effect of KI addition on the inhibition efficiency was carried out using potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy and surface analysis (scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDAX)) techniques. Results show that EMTFB suppresses low carbon steel dissolution in the corrosive environment. Inhibition efficiency increased with the increase in EMTFB concentration. Addition of iodide ions to EMTFB raises inhibition efficiency from 75 to 98%. PDP results indicate that EMTFB affects majorly anodic reactions while EMTFB + KI act as cathodic-type inhibitor. The adsorption of EMTFB onto low carbon steel surface is by physical adsorption mechanism and follows Langmuir adsorption isotherm model. SEM and EDAX results confirm the adsorption of EMTFB alone and in combination with KI onto the steel surface.     

Corrosion inhibition of mildsteel in sulphuric acid by methanol extract of Luffa aegyptiaca leaves – electrochemical and statistical view

An electrochemical and statistical view of methanol extract of Luffa aegyptiaca leaves (MLA) on the corrosion inhibition of mild steel (MS) in 0.5 M H₂SO₄ medium were investigated by potentiodynamic polarisation and electrochemical impedance spectroscopy. Polarization studies showed that the MLA acts as mixed type inhibitor with predominant cathodic behaviour. The percentage inhibition efficiency was found to increase with MLA concentration and decreased with the temperature. Thermodynamic parameter such as free energy value was negative, that indicates spontaneous adsorption of inhibitor on MS surface. Adsorption of MLA was found to obey Langmuir isotherm. The analysis of variance studies showed that the inhibition efficiencies calculated from the different electrochemical parameters are statistically significant. Surface studies were performed by Fourier transform infrared spectroscopy and atomic force microscopy.     

BIOMASS EXTRACTS FOR MATERIALS PROTECTION: CORROSION INHIBITION OF MILD STEEL IN ACIDIC MEDIA BY Terminalia chebula EXTRACTS

The inhibiting action of the fruit extract of Terminalia chebula (TC) on mild steel corrosion in 1 M HCl solution was studied using gravimetric, potentiodynamic polarization, and electrochemical impedance spectroscopy (EIS) techniques. The experimental results showed that TC functioned as an inhibitor in the acidic corrodent and that corrosion inhibition efficiency increased with extract concentration. Cathodic and anodic polarization curves show that TC functioned as a mixed-type inhibitor, while impedance results show that the extract organic matter was adsorbed at the metal/corrodent interphase. A computational study of the adsorption behavior of some of the organic constituents of the extracts was carried out using density functional theory (DFT). The computations were used to theoretically ascertain the individual contributions of the constituents to the observed corrosion-inhibiting effect of the extract.     

Corrosion inhibition of mild steel in sulphuric acid using a bicyclic thiadiazolidine

The inhibitory effect of 3a,6a-diphenyltetrahydro-1H-imidazo [4,5-c] [1, 2, 5] thiadiazole-5(3H)-thione 2,2-dioxide (TTU) on the corrosion behaviour of mild steel in 0.5 M H₂SO₄, at (30 ± 0.5) °C was studied by gravimetric, potentiodynamic polarization, electrochemical impedance spectroscopy, and scanning electron microscopy measurements. The effect of inhibitor concentration on the corrosion rate, surface coverage and inhibition efficiency is investigated. Results show that TTU exerts a strong inhibiting effect on mild steel corrosion and acts as a cathodic-type inhibitor. TTU does not affect the mechanism of the cathodic reaction while the anodic reaction mechanism changes upon addition of the inhibitor. Possible mechanistic pathways for the inhibition process are proposed. The inhibition efficiency of TTU may be due to either the adsorption of inhibitor molecules building a protective film or the formation of an insoluble complex of the inhibitor with metal cations. TTU adsorption obeys the Langmuir model.     

Adsorption and corrosion inhibition behaviour of N-(phenylcarbamothioyl)benzamide on mild steel in acidic medium

Corrosion inhibition property of N-(phenylcarbamothioyl)benzamide (PCB) on mild steel in 1.0 M HCl solution has been investigated using chemical (weight loss method) and electrochemical techniques (potentiodynamic polarization and AC impedance spectroscopy). The inhibition efficiencies obtained from all the methods are in good agreement. The thiourea derivative is found to inhibit both anodic and cathodic corrosion as evaluated by electrochemical studies. The inhibitor is adsorbed on the mild steel surface according to Langmuir adsorption isotherm. The adsorption mechanism of inhibition was supported by spectroscopic (UV-visible, FT-IR, XPS), and surface analysis (SEM-EDS) and adsorption isotherms. The thermodynamic parameter values of free energy of adsorption (ΔG_ads) reveals that inhibitor was adsorbed on the mild steel surface via both physisorption and chemisorption mechanism.     

Corrosion inhibitory action of Commiphora caudata extract on the mild steel corrosion in 1 M H2SO4 acid medium

Corrosion inhibitory action of Commiphora caudata extract on the mild steel corrosion in 1 M H₂SO₄ acid medium is investigated by weight loss and electrochemical studies. The weight loss method shows that the inhibition efficiency increases with the increase of inhibitor concentration, time, and temperature. The polarization studies reveal that the extract acts as a mixed type inhibitor. In electrochemical impedance measurement, the semicircle curves indicated that the charge transfer process controlled the corrosion of mild steel. Thermodynamic parameter such as free energy value was negative, that indicates spontaneous adsorption of inhibitor on mild steel surface. In the presence of inhibitor decreases the activation energy value which shows the chemical adsorption. The Commiphora caudata extract is found to obey Langmuir adsorption isotherm. Scanning electron microscopy, FTIR, and Quantum chemical studies confirmed that the mild steel protect from the corrosion by adsorption of the inhibitor molecules on surface of metal.     

Assessment of glycine derivative N-benzylidine-2((2-oxo-2-(10H-phenothiazine-10yl)ethyl)amino) acetohydrazide as inhibitor for mild steel corrosion in 1 M HCl solution: electrochemical and theoretical approach

Corrosion is a severe challenge which restricts the use of mild steel (MS) in various application where it comes in contact with aggressive chemicals and conditions. In this regard, different inhibitors were chosen, but environment unfriendliness of such inhibitors is a primary cause of concern. In this study, we present the systematic investigation of an environmentally benign compound, a glycine derivative N-benzylidine-2((2-oxo-2-(10H-phenothiazine-10yl)ethyl)amino) acetohydrazide (BPAA), as potential corrosion inhibitor at different temperature (30, 40, 50, and 60 °C). The investigation is accomplished by using the techniques including electrochemical polarization, electrochemical impedance spectroscopy (EIS), gravimetric, UV-visible spectrophotometry, FT-IR spectroscopy. The morphological characterization of the samples has been done by using high resolution SEM. The evaluated compound works as effective inhibitor for acid corrosion at substantially lower concentration and its adsorption on the MS surface was found to followed the Langmuir adsorption isotherm. Calculated thermodynamic parameters for adsorption unveiled a strong interaction amongst the inhibitor-MS surface. The electrochemical results revealed that the inhibitor act as mixed-type. The corrosion inhibition efficiency (IE) of the inhibitor was synergistically enhanced in the presence of surfactant additives sodium dodecyl sulfate and cetyl pyridinium chloride at quite lower concentration and showed that the addition of surfactant is an alternate strategy to enhance the IE and reduce the cost. The order of IE acquired from experimental results is successfully verified by theoretical calculations.     

Inhibition of Steel Corrosion in Nitric Acid by Sulfur Containing Compounds

The inhibitive mechanism, thermodynamics, and adsorptive properties of thiobarbituric acid (TBA) and thiourea (TU) on the corrosion of mild steel in 0.5 M HNO₃ solution have been investigated using potentiodynamic, electrochemical impedance spectroscopy techniques, and quantum chemical calculations. Both inhibitors showed good inhibition efficiency in nitric acid solution. TU was the most effective inhibitor and its inhibition efficiency increases with increasing concentration to attain 99% at 6 × 10^?3 mol · L^?1 at 30°C. Theoretical fitting of different isotherms, Langmuir, Flory–Huggins, Temkin, and the kinetic-thermodynamic models were tested to clarify the nature of inhibitors adsorption on mild steel surface. The obtained experimental data fitted all the applied adsorption isotherms except Langmuir. The thermodynamic activation parameters were determined to provide evidence of the inhibitory effect of TBA and TU. To determine the surface charge at the steel surface in nitric acid solution the potential of zero charge was measured using AC measurements at different potentials. Quantum chemical parameters were calculated and explained. The data clarified that the inhibition of steel in nitric acid by TU or TBA takes place through physicochemical adsorption mechanism.     

CHAMOMILE (Matricaria recutita) EXTRACT AS A CORROSION INHIBITOR FOR MILD STEEL IN HYDROCHLORIC ACID SOLUTION

The corrosion inhibition of mild steel in hydrochloric acid solution by chamomile (Matricaria recutita) extract (CE) was investigated through electrochemical (polarization, EIS) and surface analysis (optical microscopy/AFM/SEM) techniques. The effects of inhibitor concentration, temperature, and pH were evaluated. Thermodynamic parameters were calculated and adsorption studies were carried out. Finally, the surface morphology was investigated. The electrochemical studies showed that CE acts as a mixed-type corrosion inhibitor with predominantly anodic behavior. CE was adsorbed physically on the metal surface and obeyed the Langmuir adsorption isotherm. It impeded the corrosion processes by changing the activation energy. In the presence of CE, the metal surface was more uniform than the surface in the absence of inhibitor. Maximum inhibition efficiency (IE) was 93.28%, which was obtained at 22°C in 7.2 g/L of inhibitor in 1 M HCl solution.     

Electrochemical study on the effect of bipyridine dicarboxylic acid and its cobalt complex on the corrosion behaviour of carbon steel in acidic medium

The 2,2′-bipyridine-3,3′-dicarboxylic acid (bida) and its cobalt complex (Co-bida) were tested as corrosion inhibitors for N80 carbon steel in sulphuric acid solution by electrochemical polarization and electrochemical impedance spectroscopy method. The results indicate that the complex and ligand inhibit the corrosion of mild steel in H₂SO₄ solutions and the extent of inhibition increases with inhibitor concentration and decreases with temperature. The inhibition efficiency of the inhibitors follows the trend Co-bida > bida. A mixed-inhibition mechanism is proposed for the inhibitive effects of the compounds. The adsorption characteristics of the inhibitors were approximated by Temkin isotherm. Morphological study of the carbon steel electrode surface was undertaken by scanning electron microscope and the interfacial species formed on the surface in the presence of inhibitors analyzed by infrared spectroscopy.     

Investigation of corrosion inhibitory effect of hydroxyl propyl alginate on mild steel in acidic media

The anti‐corrosion effect of hydroxyl propyl alginate (HPA) on mild steel in 1M HCl has been studied by chemical (weight loss) and electrochemical (polarization and electrochemical impedance spectroscopy) methods. From all the three methods, it is inferred that there is an increase in inhibition efficiency with increase in concentration of the inhibitor. Polarization studies revealed the mixed mode of inhibition by HPA. The mode of adsorption is physical in nature. The adsorption of HPA on mild steel followed Frumkin adsorption isotherm. The thermodynamic and kinetic parameters have been calculated and discussed. Surface morphological studies have been carried out with Scanning electron microscopy (SEM) and Atomic force microscopy (AFM). Fourier transform infrared spectroscopy (FTIR) is utilized to characterize the adsorbed film. SEM and AFM methods confirm the presence of inhibitor on the surface of the metal. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43004.     

INHIBITION OF MILD STEEL CORROSION IN SULFURIC ACID MEDIUM BY HYDROXYETHYL CELLULOSE

The inhibitive effect of hydroxyethyl cellulose (HEC) on mild steel corrosion in aerated 0.5 M H₂SO₄ solution was studied using gravimetric and electrochemical techniques. The effect of temperature on corrosion and inhibition was also investigated. The results show that hydroxyethyl cellulose functioned as a good inhibitor in the studied environment and inhibition efficiency increased with concentration of inhibitor. Potentiodynamic polarization measurements revealed that HEC inhibited both the cathodic and anodic partial reactions of the corrosion processes. Impedance results clearly show that HEC inhibited the corrosion reaction by adsorption onto the metal/solution interface by significantly decreasing the double layer capacitance (C _dl ). This result was greatly pronounced in the presence of the inhibitor system (HEC + KI) that contains halide additive. Temperature studies revealed an increase in inhibition efficiency with rise in temperature. The adsorption behavior was found to obey the Freundlich isotherm. The values of activation energy, heat of adsorption, and standard free energy suggest that there was transition from physical to chemical adsorption mechanism of HEC on the mild steel surface. Quantum chemical calculations using the density functional theory (DFT) was employed to determine the relationship between molecular structure and inhibition efficiency.     

Chitosan Schiff base as eco-friendly inhibitor for mild steel corrosion in 1 M HCl

In the present study, natural biopolymer chitosan was modified into its Schiff base derivative with salicylaldehyde by condensation method. The prepared chitosan salicylaldehyde Schiff base was characterized using ultraviolet spectroscopy, fourier transform infrared spectroscopy, scanning electron microscope and elemental analysis. Thermal analysis was also carried out to determine the thermal stability of the derivative. To explore the corrosion inhibition performance of the chitosan Schiff base, weight loss, and electrochemical techniques were conducted. The inhibitor reduces the metallic corrosion by adsorbing on to the metal surface. The adsorption of chitosan Schiff base on mild steel surface in 1 M HCl follows Temkin isotherm model. Thermodynamic parameters of adsorption and corrosion process were calculated, which revealed the chemical nature of adsorption. SEM and energy dispersive X-ray spectroscopic analysis confirmed the formation of protective chitosan derivative layer on the mild steel surface.     

Corrosion inhibition effect of pyrazole derivatives on mild steel in hydrochloric acid solution

Synthesized compounds, namely methyl 5-(4-Chlorobenzoyloxy)-1-phenyl-1H-pyrazole-3-carboxylate (MCPPC) and 5-(4-methoxyphenyl)-3-(4-methylphenyl)4,5-dihydro-1H-pyrazol-1-yl-(pyridin-4-yl)methanone (MMDPPM) were investigated as corrosion inhibitor for mild steel (MS) in 15% HCl solution using weight loss measurement, potentiodynamic polarization, and electrochemical impedance spectroscopy (EIS) methods. Inhibition efficiency was found concentration-dependent and increased by increasing the concentration of MCPPC and MMDPPM. Both of inhibitors were efficient even at a very low concentration of 25 ppm. The inhibitors MCPPC and MMDPPM showed inhibition efficiency of 67.1 and 76.8%, respectively, at 25 ppm, whereas it was 92.0 and 95.9%, respectively, at 250 ppm concentration at 303 K. The potentiodynamic polarization curves showed that MCPPC and MMDPPM act as mixed-type inhibitor in 15% HCl solution. The Nyquist plots showed that charge transfer resistance increased and double-layer capacitance decreased on increasing the concentration of studied inhibitors due to adsorption of inhibitor molecules on MS surface. The adsorption of each inhibitor on MS surface obeys Langmuir adsorption isotherm. On the basis of thermodynamic adsorption parameters, mixed-type adsorption (physisorption and chemisorption) for the studied inhibitors on MS surface was suggested. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and atomic force microscopy (AFM) analyses confirmed the existence of a protective film of the inhibitor on MS surface. The density functional theory was employed for theoretical calculations, and the obtained results were found to be consistent with the experimental findings.