Corrosion inhibition of mild steel in hydrochloric acid solution by some double Schiff bases

The inhibition effect of four double Schiff bases on the corrosion of mild steel in 2 M HCl has been studied by polarization, electrochemical impedance spectroscopy (EIS) and weight loss measurements. The inhibitors were adsorbed on the steel surface according to the Langmuir adsorption isotherm model. From the adsorption isotherm, some thermodynamic data for the adsorption process were calculated and discussed. Kinetic parameters activation such as E_a, ΔH∗, ΔS∗ were evaluated from the effect of temperature on corrosion and inhibition processes. Quantum chemical calculations have been performed and several quantum chemical indices were calculated and correlated with the corresponding inhibition efficiencies.     

Investigation of the effect of disulfiram on corrosion of mild steel in hydrochloric acid solution

The corrosion inhibition properties of disulfiram (DSR) for mild steel in HCl solution were analyzed by electrochemical impedance spectroscopy (EIS), potentiodynamic polarization, atomic force microscopy, scanning electron microscopy and gravimetric methods. Physical adsorption is proposed for the inhibition and the process followed the Langmuir adsorption isotherm and kinetic/thermodynamic model of El-Awady et al. Constant phase elements describing the non-ideal characteristics of the electrochemical interface are introduced. The occurrence of inductive loop is also dealt with, through the introduction of an inductive element L. The use of these elements significantly improved the quality of fit of simulation to the EIS data.     

Carbon steel corrosion inhibition in hydrochloric acid solution using a reduced Schiff base of ethylenediamine

The behavior of the Schiff base N,N′-bis(salicylidene)-1,2-ethylenediamine (Salen), its reduced form (N,N′-bis(2-hydroxybenzyl)-1,2-ethylenediamine) and a mixture of its preceding molecules, ethylenediamine and salicylaldehyde, as carbon steel corrosion inhibitors in 1 mol L⁻¹ HCl solution was studied by corrosion potential measurements, potentiodynamic polarization curves, electrochemical impedance spectroscopy and spectrophotometry measurements. The experimental results showed that the reduced Salen presented the highest efficiency among the inhibitors studied. The results obtained in the presence of Salen were similar to those obtained in the presence of the salicylaldehyde and ethylenediamine mixture, showing that in acid medium the Salen molecule undergoes hydrolysis, regenerating its precursor molecules.     

Investigation on some Schiff bases as corrosion inhibitors for mild steel

In the present work, the effect of some newly synthesized Schiff bases containing sulphur nitrogen as heteroatom was investigated on mild steel corrosion in acidic media. Electrochemical studies of the mild steel samples were performed in an aerated solution of 0.1 M HCl + dimethyl sulphoxide (DMS) as co-solvent. DMS is also behaving as a corrosion inhibitor for mild steel. At low inhibitor concentration and short immersion time one can see only the inhibitive effect of DMS as anodic inhibitor for mild steel. At high concentration and long immersion time inhibition efficiencies are increased and cathodic inhibition is observed.     

The effect of some bis-thiadiazole derivatives on the corrosion of mild steel in hydrochloric acid

The inhibition effect of bis-thiadiazole derivatives (BTDs) against the corrosion of mild steel in 1 M HCl solution was studied by weight loss, electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization methods. All the BTDs exhibited >90% inhibition efficiency at concentration as low as 40 ppm. The adsorption of BTDs obeyed Langmuir adsorption isotherm. Both thermodynamic and activation parameters were calculated and discussed. Polarization curves indicate that they are mixed type of inhibitors. All the BTDs were adsorbed physically at lower concentration where as chemisorption was favoured at higher concentration.     

A comparative study on the corrosion behaviour of 304 austenitic stainless steel in sulfamic and sulfuric acid solutions

Potentiodynamic polarization and EIS have been employed to compare the corrosion behaviour of 304 stainless steel in NH₂SO₃H and H₂SO₄ solutions. Corrosion tests were carried out as a function of the acid’s concentration (0.1-0.5 M) and solution temperature (20-60 ^oC). The corrosion rate is higher in H₂SO₄ than in H₂NSO₃H in all concentrations and temperatures. Values of the activation energy (E_a) revealed that the corrosion process is faster in H₂SO₄ than in NH₂SO₃H solution. EIS data showed that the display of Nyquist plots, and hence the mechanism of corrosion, depends not only on the acid concentration but also on the solution temperature. In 0.1 M concentration, the equivalent circuits R_e(R_ctQ_dl) and R_e(R_ctQ_dl)(RQ)_ads describe the corrosion systems in H₂NSO₃H and H₂SO₄ solutions respectively. At concentrations ?0.2 M, the equivalent circuit R_e(R_ctQ_dl)Q_diff is applicable. Adsorption of the counter ion of the acid on the steel surface and the stability of the surface complex may explain the observed corrosion rates.     

Influence of ultrasound on pitting corrosion and crevice corrosion of SUS304 stainless steel in chloride sodium aqueous solution

The change of polarization curves and surface morphologies of SUS304 stainless steel was investigated in 3.5 mass% NaCl solution with or without the application of ultrasound (US). As the result, both the pitting corrosion and the crevice corrosion were largely suppressed by the application of US. The reason is attributed to the decrease in the concentration of hydrogen and chloride ions in pits or in the crevice by removing the corrosion product and stirring the liquid there.     

Inhibition effects of some Schiff’s bases on the corrosion of mild steel in hydrochloric acid solution

The corrosion inhibition effect of 4-{[(1Z)-(2-chloroquinolin-3-yl)methylene]amino} phenol (CAP), N-[(1Z)-(2-chloroquinolin-yl)methylene]-N-(4-methoxyphenyl)amine (CMPA) and N-[(1E)-(2-chloroquinolin-3-yl)methylene]-N-(4-nitrophenyl)amine (CNPA) on mild steel in 1.0 M HCl has been investigated using mass loss, polarization and electrochemical impedance techniques at 300 K. The inhibition efficiencies increased with increase in inhibitors concentration. Polarization studies showed that the inhibitors are of predominantly cathodic character. Among the three compounds studied, CAP exhibited the best performance giving more than 97% IE. Some samples of mild steel were examined by SEM. All the inhibitors were found to adsorb on the mild steel surface according to the Langmuir adsorption isotherm.     

Schiff bases of increasing complexity as mild steel corrosion inhibitors in 2 M HCl

The effect of three Schiff base compounds with increasing number of coordination sites, namely, 2-{(E)-[(2-hydroxyethyl)imino]methyl} phenol (I), 2-[(E)-({2-[(2-hydroxyethyl)amino]ethyl}imino)methyl]phenol (II) and 2,2′-{iminobis[ethane-2,1-diylnitrilo(E)methylylidene]}diphenol (III) have been investigated at 298 K by weight loss measurements, potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) methods. The inhibition efficiencies obtained from all methods employed are in good agreement. Results show compound III to be the best inhibitor with a mean efficiency of 93% at 10⁻² M additive concentration. Studies showed all three compounds to act as mixed type inhibitors.     

Inhibitive effect of diethylcarbamazine on the corrosion of mild steel in hydrochloric acid

Potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), weight loss measurements and atomic force microscopy techniques were used to investigate the inhibitory effect of diethylcarbamazine (DECM) on corrosion of mild steel in HCl solution. The inhibitor showed >90% inhibition efficiency at 5.01 × 10⁻⁴ M. Results obtained revealed that inhibition occurs through adsorption of inhibitor molecules on metal surface without modifying the mechanism of corrosion process. Potentiodynamic polarization studies suggested that it is a mixed type inhibitor, predominantly controls cathodic reaction. Activation parameters (E_a, ΔH and ΔS) and thermodynamic parameters (, and ) were calculated to investigate mechanism of inhibition.     

Thermodynamic, electrochemical and quantum chemical investigation of some Schiff bases as corrosion inhibitors for mild steel in hydrochloric acid solutions

The corrosion inhibition of mild steel in 1.0 M HCl solution by four Schiff bases was investigated using weight loss and electrochemical measurements and quantum chemical calculations. All compounds showed >90% inhibition efficiency at their optimum concentrations. The activation energy (E_a) of corrosion and other thermodynamic parameters were calculated to elaborate the mechanism of corrosion inhibition. The adsorption of the inhibitors on the mild steel surface follows Langmuir isotherm model. Polarization studies indicated that all studied inhibitors are mixed type. The computed quantum chemical properties viz., electron affinity (EA) and molecular band gap (ΔE_MBG) show good correlation with experimental inhibition efficiencies.     

Inhibition of the corrosion of steel in hydrochloric acid solution by some organic molecules containing the methylthiophenyl moiety

The corrosion inhibition effect of 2-[4-(methylthio) phenyl] acetohydrazide (HYD), 2-{[4-(methylthio) phenyl] acetyl} hydrazinecarbothioamide (TAD) and 5-[4-(methylthio) benzyl]-4H-1,2,4-triazole-3-thiol (TRD) on steel in 1.0 M HCl was investigated by mass loss and electrochemical methods. The effect of concentration, temperature and immersion time was studied. The results indicated that the compounds are efficient, mixed type and pursue Flory–Huggins adsorption isotherm. The inhibition efficiency at lower concentration of inhibitor decreased with temperature while at higher concentration, it is retained and the calculated free energy attributes this to comprehensive adsorption. The efficiency stands in the order TRD > TAD > HYD and is confirmed by the Quantum studies.     

Blue tetrazolium as a novel corrosion inhibitor for cold rolled steel in hydrochloric acid solution

The inhibition effect of blue tetrazolium (BT) on the corrosion of cold rolled steel (CRS) in 1.0 M HCl solution at 20 °C was investigated by weight loss, potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), and scanning electron microscopy (SEM) methods. The results show that BT is a very good inhibitor, and the adsorption of BT on CRS surface obeys Langmuir adsorption isotherm. Polarization curves reveal that BT acts as a mixed-type inhibitor. EIS spectra exhibit one capacitive loop and confirm the inhibitive ability. The inhibition action of BT is also evidenced by SEM images.     

Effects of dithionite ion on corrosion of type 304 stainless steel in sulphuric acid solution

Corrosion behaviour of type 304 stainless steel was investigated, with particular attention to additive effects of hydrosulphite (Na₂S₂O₄) on corrosion in 0.1 mol/l H₂SO₄ solution with various amounts of Na₂S₂O₄ up to 60 mmol/l.Corrosion of SUS304 occurred below pH 3.0 at 30 °C in a 0.1 mol/l H₂SO₄ solution in which Na₂S₂O₄ was added to 0.1-20 mmol/l. The maximum corrosion rate at 30 °C was measured as 7.2 g/m² h (7.9 mm/y) in 0.1 mol/l H₂SO₄-10 mmol/l Na₂S₂O₄ at pH 1.2. Microscopic surface observation revealed that active dissolution was accompanied by intergranular corrosion at the metal surface.The SUS304 was easily passivated in 0.1 mol/l H₂SO₄ solution with more than 30 mmol/l Na₂S₂O₄. NiS was detected in the passivated film.     

Effects of temperature on the oxide film properties of 304 stainless steel in high temperature lithium borate buffer solution

The paper mainly investigated the effects of temperature on the oxide film properties of 304SS in lithium borate buffer solution by electrochemical measurements and XPS analysis. As temperature increased, the protective property of the film degraded and structure varied from a single layer to a double-layer. Whatever the temperature, the oxide film exhibited an n-type and p-type semiconductor in the potential range above and below the flat band potential, respectively. The electronic properties were assigned to a Fe–Cr spinel inner layer and a defective Fe–Cr oxide outer layer. The related growth mechanisms of the oxide film were also discussed.     

Influence of peening on the corrosion properties of AISI 304 stainless steel

The effects of peening treatment on the microstructure and corrosion behavior of AISI 304SS were investigated. Shot and ultrasonic peening were performed on the austenitic stainless steel, and peened specimens were compared in terms of microstructure, surface roughness and corrosion resistance. Nano-sized grains, multi-directional mechanical twins and strain-induced martensite were formed on the surfaces, and the volume fraction of strain-induced martensite in the ultrasonically peened specimen was higher than that of the shot-peened specimen. The ultrasonically peened specimen which had smoother surface and contained more strain-induced martensite showed superior general and localized corrosion resistance to the as-received and shot-peened specimens.     

Adsorption and inhibitive properties of some new Mannich bases of Isatin derivatives on corrosion of mild steel in acidic media

Adsorption of four derivatives of piperidinylmethylindoline-2-one on mild steel surface in 1 M HCl solution and its corrosion inhibition properties has been studied by a series of techniques, such as polarization, electrochemical impedance spectroscopy (EIS), weight loss and quantum chemical calculation methods. The values of activation energy (E_a) for mild steel corrosion and various thermodynamic parameters were calculated and discussed. Potentiodynamic polarization measurements showed that all inhibitors are mixed type. The degree of surface coverage was determined by using weight loss measurements and it was found that adsorption process of studied inhibitors on mild steel surface obeys Langmuir adsorption isotherm.     

Influence of input power to vibrator and vibrator-to-specimen distance of ultrasound on pitting corrosion of SUS304 stainless steel in 3.5% chloride sodium aqueous solution

The pitting corrosion of SUSU304 steel can be suppressed by the application of a 19.5 kHz ultrasound (US) in 3.5% NaCl aqueous solution. At a constant vibrator-to-specimen distance of d = 76 mm equal to the wavelength, the suppression effect increased with the input power to vibrator and the largest effect was obtained at the power of I = 8. At constant input powers of I = 2 or 8, the suppression effect decreased with the increase in the vibrator-to-specimen distance, but the largest effect was obtained at d = 68 mm in each case of I = 2 and 8.     

Theoretical and electrochemical assessment of inhibitive behavior of some thiophenol derivatives on mild steel in HCl

Inhibitive performance of some synthesized thiophenol derivatives on corrosion behavior of mild steel in 0.1 M HCl solution was investigated by means of electrochemical techniques, quantum chemical and optical microscopy. The increase in concentration and immersion time shows a positive effect on inhibition efficiency while temperature has a negative effect. Inhibitor molecules directly adsorb at surface on the basis of donor–acceptor interactions between the π-electrons of benzene, sulfur and nitrogen atoms and the vacant d-orbitals of iron atoms. According to the thermodynamic parameters, present inhibitors adsorb physically. Optical microscopy examinations demonstrate a decrease in corrosion attacks in presence of inhibitors.     

Acid violet 6B as a novel corrosion inhibitor for cold rolled steel in hydrochloric acid solution

The inhibition effect of acid violet 6B (AV6B) on the corrosion of cold rolled steel (CRS) in 1.0–5.0 M HCl solution was studied for the first time by weight loss, potentiodynamic polarization, and electrochemical impedance spectroscopy (EIS) methods. The results show that AV6B is a very good inhibitor in 1.0 M HCl, and the adsorption of AV6B on CRS surface obeys Langmuir adsorption isotherm. Polarization curves reveal that AV6B behaves as a mixed-type inhibitor. EIS spectra exhibit one capacitive loop and confirm the inhibitive ability. Effects of immersion time and acid concentration on inhibition performance were also discussed.