Effect of hexamethylpararosaniline chloride (crystal violet) on mild steel corrosion in acidic media

The corrosion inhibition of mild steel in 0.5 M H₂SO₄ and 1 M HCl by hexamethylpararosaniline chloride (HMPC) was investigated using the gravimetric technique in the temperature range 303–333 K. The results indicate that HPMC inhibited the corrosion reaction in both acid media at all temperatures and inhibition efficiency increased with HMPC concentration. The inhibiting action is attributed to general adsorption of protonated and molecular HPMC species on the corroding metal surface. Adsorption followed a modified Langmuir isotherm and the Temkin isotherm, with very high negative values of the free energy of adsorption (). An increase in temperature reduced the inhibition efficiency of HPMC in 0.5 M H₂SO₄ but increased efficiency in 1 M HCl. Activation parameters such as activation energy (E_a), activation enthalpy (ΔH^∗) and activation entropy (ΔS^∗) as well as the adsorption heat (Q_ads) were evaluated from the effect of temperature on corrosion and inhibition processes.     

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.     

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.     

The role of some thiosemicarbazide derivatives as corrosion inhibitors for C-steel in acidic media

Corrosion inhibition of C-steel in 2 M HCl was investigated in the absence and presence of different concentrations of some thiosemicarbazide derivatives namely, 1-ethyl-4(2,4-dinitrophenyl) thiosemicarbazide (I), 1,4-diphenylthiosemicarbazide (II), 1-ethyl-4-phenylthiosemicarbazide (III). Weight loss, potentiodynamic polarization and electrochemical impedance spectroscopy techniques were employed. Impedance measurements showed that the double-layer capacitance decreased and charge-transfer resistance increased with increase in the inhibitors concentration and hence increasing in inhibition efficiency. Potentiodynamic polarization study showed that all the inhibitors act as mixed-type inhibitors. Results obtained reveal that the inhibition efficiency (%IE) follows the sequence: I > II > III. The adsorption of these compounds on C-steel surface obeys Temkin’s adsorption isotherm and has a chemisorptions mechanism.     

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.     

Substitutional adsorption isotherms and corrosion inhibitive properties of some oxadiazol-triazole derivative in acidic solution

A newly synthesized oxadiazol-triazole derivative (TOMP), was investigated as corrosion inhibitor of mild steel in 0.5 M H₂SO₄ solution using weight loss measurements, polarization and electrochemical impedance spectroscopy (EIS) methods. Results obtained revealed that TOMP is effective corrosion inhibitor for mild steel in sulphuric acid and its efficiency attains more than 97.6% at 298 K. The number of water molecules (X) replaced by a molecule of organic adsorbate was determined from the substitutional adsorption isotherms applied to the data obtained from the weight loss experiments performed on mild steel specimen in acidic solution in the 298-333 K range.     

Design and synthesis of a novel class of inhibitors for mild steel corrosion in acidic and carbon dioxide-saturated saline media

p-(9-(2-Methylisoxazolidin-5-yl)nonyloxy)benzaldehyde I, prepared using a cycloaddition protocol, was elaborated into its cinnamaldehyde derivative II which upon quarternization with propargyl chloride afforded III bearing an interesting blend of structural traits suitable for imparting inhibition of mild steel corrosion. Novel compounds I–III showed efficient inhibition against mild steel corrosion in CO₂–0.5 M NaCl (40 °C, 1 atm; 120 °C, 10 bar), 1, 4, 7.7 M HCl, and 0.5 M H₂SO₄ at 60 °C as determined by gravimetry and electrochemical methods. The presence of carbonaceous surface and nitrogen, as revealed by XPS study, indicated the formation of a film covering the metal surface, which imparted corrosion inhibition.     

Correlation between corrosion rate and AE signal in an acidic environment for mild steel

The AE method is an effective technique for inspecting corrosion damage of mild steel, such as tank bottom floors. However, the correlation between AE signals and corrosion behaviour for mild steel has not yet been fully clarified. In the present study, the authors considered that the corrosion regions of bottom floors become a strong acid environment by Cl⁻, as reported in a previous study. Thus, the polarization resistance for the test pieces of mild steel was measured with an AC impedance method under a strong acid environment. It was clear that the polarization resistance indicated the corrosion rate for a test piece of mild steel in the experiments. While measuring the AE signals, the corrosion rate was monitored with a test piece. As a result, the AE signal showed good correlation with the corrosion rates of the test pieces. The corrosion behaviour of the test pieces was then discussed with the corrosion potential measured during the experiments. Furthermore, the cathode current was changed to control the generated hydrogen gas volume. The volume of the hydrogen gas generated from the cathode reaction was correlated to the AE signals.     

Experimental and theoretical studies for mild steel corrosion inhibition in 1 M HCl by two new benzothiazine derivatives

The inhibition effect of new heterocyclic compounds, namely 2-aryl-benzothiazin-3-one (P1) and 3-aryl-benzothiazin-2-one (P2) on mild steel corrosion in 1 M HCl was investigated using electrochemical measurements. The results indicated that the inhibition efficiency depends on concentration and molecular structure of the investigated compounds. It is also found that the inhibition of P1 is greater than P2. The molecular structure effect on the corrosion inhibition efficiency was investigated using DFT calculations. The structural and electronic parameters were calculated and discussed. The obtained results show that the experimental and theoretical studies agree well and confirm that P1 is the better inhibitor.     

Novel benzimidazole derivatives as corrosion inhibitors of mild steel in the acidic media. Part I: Gravimetric,electrochemical, SEM and XPS studies

Three novel benzimidazole derivatives, 2-aminomethyl benzimidazole (ABI), bis (2-benzimidazolylmethyl) amine (BBIA) and tri (2-benzimidazolylmethyl) amine (TBIA), have been studied as inhibitors for mild steel in 1.0 M HCl. The three compounds prevent mild steel from corrosion by adsorption on the steel surface and forming insoluble complex with ferrous species. Inhibition efficiency increases with the increase in the number of benzimidazole segments in the molecules (TBIA > BBIA > ABI). Protection efficiency of the inhibitors depends on concentration of inhibitor, temperature and concentration of hydrochloric acid.     

The effect of two oleo-gum resin exudate from Ferula assa-foetida and Dorema ammoniacum on mild steel corrosion in acidic media

A comparative study of two oleo-gum resins exudate from Ferula assa-foetida (F. assa-foetida) and Dorema ammoniacum (D. ammoniacum), as inhibitors for mild steel corrosion in 2 M HCl solution was investigated by weight loss measurements, potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) methods. Potentiodynamic polarization curves indicated that both oleo-gums behave as mixed type inhibitors. The effect of temperature on the inhibition efficiency was studied. At all temperatures, the experimental data fit Langmuir isotherm for both oleo-gum resin exudates. Quantum chemical calculations were performed to illustrate the adsorption process of some specific components of two oleo-gum resin exudates.     

Inhibition effects of 2,5-dimercapto-1,3,4-thiadiazole on the corrosion of mild steel in sulphuric acid solution

The effect of 2,5-dimercapto-1,3,4-thiadiazole (DMTD) on the corrosion of mild steel (MS) in 1.0 M H₂SO₄ was investigated. DMTD acted as a mixed-type inhibitor without change of the mechanism of hydrogen evolution. The inhibition efficiency increased with the increase in concentration of DMTD but decreased with the increase of temperature. Adsorption of the inhibitor on the MS surface obeyed the Langmuir adsorption isotherm. The potential of zero charge suggests MS surface is positively charged in 1.0 M H₂SO₄. Thermodynamics and quantum chemical calculations reveal that the adsorption process of DMTD includes electrostatic interaction and electron donor–acceptor interactions.     

Inhibition of mild steel corrosion in acid solution by Pheniramine drug: Experimental and theoretical study

Inhibition of mild steel corrosion in 1 M HCl solution by Pheniramine drug was studied using weight loss, electrochemical impedance spectroscopy, linear polarization resistance, and potentiodynamic polarization measurements. The values of activation energy (E_a) and different thermodynamic parameters such as adsorption equilibrium constant (K_ads), free energy of adsorption , adsorption enthalpy and adsorption entropy were calculated and discussed. The adsorption process of studied drug on mild steel surface obeys the Langmuir adsorption isotherm. Potentiodynamic polarization measurements showed that Pheniramine is mixed-type inhibitor. Further, theoretical calculations were carried out and relations between computed parameters and experimental inhibition efficiency were discussed.     

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.     

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.     

Evaluation of the inhibitive effect of some plant extracts on the acid corrosion of mild steel

Corrosion inhibition of mild steel in 2 M HCl and 1 M H₂SO₄ by extracts of selected plants was investigated using a gasometric technique at temperatures of 30 and 60 °C. The studied plants materials include leaf extracts Occimum viridis (OV), Telferia occidentalis (TO), Azadirachta indica (AI) and Hibiscus sabdariffa (HS) as well as extracts from the seeds of Garcinia kola (GK). The results indicate that all the extracts inhibited the corrosion process in both acid media by virtue of adsorption and inhibition efficiency improved with concentration. Synergistic effects increased the inhibition efficiency in the presence of halide additives. Inhibition mechanisms were deduced from the temperature dependence of the inhibition efficiency as well as from assessment of kinetic and activation parameters that govern the processes. Comparative analysis of the inhibitor adsorption behaviour in 2 M HCl and 1 M H₂SO₄ as well as the effects of temperature and halide additives suggest that both protonated and molecular species could be responsible for the inhibiting action of the extracts.     

Cefotaxime sodium: A new and efficient corrosion inhibitor for mild steel in hydrochloric acid solution

The corrosion inhibition of mild steel in 1 M HCl solution by cefotaxime sodium has been studied by Tafel polarization, electrochemical impedance spectroscopy (EIS) and weight loss measurement. The inhibitor showed 95.8% inhibition efficiency at optimum concentration 300 ppm. Results obtained revealed that inhibition occurs through adsorption of the cefotaxime on metal surface without modifying the mechanism of corrosion process. Potentiodynamic polarization studies suggest that it is a mixed type of inhibitor. Electrochemical impedance spectroscopy techniques were also used to investigate the mechanism of corrosion inhibition.     

Electrochemical and quantum chemical studies of some azomethine compounds as corrosion inhibitors for mild steel in 1 M hydrochloric acid

The corrosion inhibition effect of new azomethine compounds: PhNNC (COCH₃)NC₆H₄Y {Y = OCH₃ (SB₁), CH₃ (SB₂), H (SB₃), Br (SB₄) and Y = Cl (SB₅)} on mild steel in 1 M HCl, was investigated using potentiodynamic polarization, electrochemical impedance spectroscopy (EIS) and quantum chemistry analysis. It has been found that the inhibition efficiency increased with increasing inhibitor concentration. The polarization curves showed that these Schiff bases function as mixed inhibitors. The adsorption of studied compounds on mild steel surface was found to follow the Langmuir isotherm. Molecular modeling was used to correlate corrosion inhibition properties and calculated quantum chemical parameters.     

Benzimidazole and its derivatives as corrosion inhibitors for mild steel in 1M HCl solution

In this paper, the inhibition ability of benzimidazole and its derivatives against the corrosion of mild steel in 1M HCl solution was studied. The change of impedance parameters observed by variation of inhibitors concentration within the range of 50-250 ppm was an indication of their adsorption. The thermodynamic adsorption parameters proposed that these inhibitors retard both cathodic and anodic processes through physical adsorption and blocking the active corrosion sites. The adsorption of these compounds obeyed the Langmuir’s adsorption isotherm. The inhibition efficiency was increased with inhibitor concentration in the order of 2-mercaptobenzimidazole > 2-methylbenzimidazole > benzimidazole, which is in accordance with the variation of apparent activation energy of corrosion.