Interaction of 12-aminododecanoic acid with a carbon steel surface: Towards the development of ‘green’ corrosion inhibitors

The inhibiting effect of 12-aminododecanoic acid (AA) on corrosion of carbon steel (CS) in CO₂-saturated hydrochloric acid was investigated. It was found that AA acts as a mixed-type inhibitor, yielding a maximum inhibition efficiency of 98.1 ± 0.1%. The mechanism of its corrosion inhibition is by formation of a self-assembled monolayer (SAM), which presents a tight hydrophobic barrier imposed by the (-CH₂)₁₁ chain. In-situ PM-IRRAS measurements revealed that the SAM is amorphous. The SAM formation process was found to be spontaneous and reversible. The corresponding standard Gibbs energy of AA adsorption on CS was calculated to be −28 kJ mol⁻¹.     

Gallic acid as a corrosion inhibitor of carbon steel in chemical decontamination formulation

Gallic acid (GA) was found to provide corrosion inhibition to carbon steel (CS) at 4.25 mM concentration. Inherent stability to radiation degradation as compared to other reductant and coupled with its anionic nature with respect to removal using ion exchange column makes it suitable for using as both reductant as well as corrosion inhibitor in dilute decontamination formulations operating in the regenerative mode. A formulation containing CA (1.4 mM), EDTA/NTA (1.4 mM), AA (1.0-2.0 mM) and GA (4.25 mM) was found to be more efficient in dissolving hematite and providing 31% corrosion inhibition (passivation) to the CS.     

Influence of flow on the corrosion inhibition of St52-3 type steel by potassium hydrogen-phosphate

Influence of hydrodynamic conditions on the corrosion of St52-3 type steel rotating disc electrode, RDE, in 3.5% NaCl and its corrosion inhibition using K₂HPO₄ have been studied. Results showed that by rotating the electrode in blank and inhibited solutions, corrosion current density, i_corr, increased, corrosion potential, E_corr, shifted toward more positive values and charge transfer resistance, R_ct, decreased. The inhibition efficiencies increased with electrode rotation rate. This increase was attributed to the enhanced mass transport of inhibitor molecules toward the metal surface and formation of more protective films. Little decrease of efficiencies at higher rotation speeds was probably because of the separation of protective films due to high shear stresses.     

Influence of iron microstructure on the performance of polyacrylic acid as corrosion inhibitor in sulfuric acid solution

The corrosion inhibition behavior of bulk nanocrystalline ingot iron (BNII) fabricated from coarse polycrystalline ingot iron (CPII) by severe rolling technique by polyacrylic acid (PAA) was studied in 0.1 M H₂SO₄ using electrochemical impedance spectroscopy and potentiodynamic polarization techniques. The results indicated that PAA inhibited the acid induced corrosion of both iron specimens, with greater effect noted for BNII. The corrosion inhibiting effect was influenced by the microstructure of the iron samples. Synergistic inhibition effect was observed on addition of iodide ions to PAA in case of CPII while for BNII inhibition efficiency marginally increased.     

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.     

Inhibition treatment of the corrosion of lead artefacts in atmospheric conditions and by acetic acid vapour: use of sodium decanoate

The efficiency of linear sodium decanoate, CH₃(CH₂)₈COONa (noted NaC₁₀), as corrosion inhibitor of lead was determined by electrochemical techniques in two corrosive mediums: ASTM D1384 standard water and acetic acid-enriched solutions. Best results were obtained with 0.05 mol l⁻¹ of NaC₁₀ solution. In these conditions, the inhibition efficiency can be estimated of 99.9%. The corrosion inhibition effect was confirmed by cyclic atmospheric tests in a climatic chamber in two different conditions: water saturated vapour, and acid acetic enriched vapour simulating the atmosphere in the wooden displays in museums. Surface analyses by SEM and X-ray diffraction indicate that the metal protection is due to the formation of a protective layer mainly composed of lead decanoate Pb(C₁₀)₂ (metallic soap). This inhibition treatment was applied on objects of metallic cultural heritage: gallo-roman sarcophagus in lead. Electrochemical methods confirm the efficiency of treatment on archaeological materials. In conclusion, this inhibitor treatment seems to be very promising against the atmospheric corrosion and the corrosion by organic acid vapour in museums.     

Experimental and theoretical investigation of 3-amino-1,2,4-triazole-5-thiol as a corrosion inhibitor for carbon steel in HCl medium

The inhibition effect of 3-amino-1,2,4-triazole-5-thiol (3ATA5T) was investigated in 0.5 M HCl on carbon steel (CS) by electrochemical impedance spectroscopy and potentiodynamic measurements at various concentrations and temperatures. Results showed that the correlation between experimental (inhibition efficiencies, ΔG_ads, E_a) and quantum calculation parameters (dipole moment, E_HOMO, E_LUMO). The high inhibition efficiency was declined in terms of strongly adsorption of protonated inhibitor molecules on the metal surface and forming a protective film.     

The inhibitive effect of some bis-N,S-bidentate Schiff bases on corrosion behaviour of 304 stainless steel in hydrochloric acid solution

The inhibition effect of four new Schiff bases on the corrosion of 304 stainless steel in 1 M HCl has been studied by polarization, electrochemical impedance spectroscopy (EIS) and weight loss measurements. Polarization curves indicated that all studied Schiff bases act as mixed type (cathodic/anodic) inhibitors. The adsorption of the inhibitors was well described by the Langmuir adsorption isotherm and the adsorption isotherm parameters (K_ads, ΔG_ads) were determined at room temperature. Effect of temperature on the efficiency of the corrosion inhibition process was studied and the values of activation energy, pre-exponential factor (λ), enthalpy of activation and entropy of activation were calculated to elaborate the mechanism of corrosion inhibition. Differences in inhibition efficiency between four tested inhibitors are correlated with their chemical structures.     

The investigation of synergistic inhibition effect of rhodanine and iodide ion on the corrosion of copper in sulphuric acid solution

The synergistic inhibition effect of rhodanine (Rdn) and iodide ion on the corrosion of copper in 0.5 M H₂SO₄ solution was studied using electrochemical techniques. The surface morphologies of the substrates were examined by scanning electron microscopy (SEM). Elemental analysis of electrode surface exposed to test solution was determined by energy dispersive X-ray spectroscopy (EDX). It was found that Rdn provided satisfactory inhibition on the corrosion of copper. Moreover, its inhibition efficiency further increased in the presence of iodide ions due to synergistic effect. Finally, a mechanism of inhibition is proposed and discussed.     

Copper corrosion inhibition in O2-saturated H2SO4 solutions

Corrosion inhibition of copper in O₂-saturated 0.50 M H₂SO₄ solutions by four selected amino acids, namely glycine (Gly), alanine (Ala), valine (Val), or tyrosine (Tyr), was studied using Tafel polarization, linear polarization, impedance, and electrochemical frequency modulation (EFM) at 30 °C. Protection efficiencies of almost 98% and 91% were obtained with 50 mM Tyr and Gly, respectively. On the other hand, Ala and Val reached only about 75%. Corrosion rates determined by the Tafel extrapolation method were in good agreement with those obtained by EFM and an independent chemical (i.e., non-electrochemical) method. The chemical method of confirmation of the corrosion rates involved determination of the dissolved Cu²⁺, using ICP-AES (inductively coupled plasma atomic emission spectrometry) method of chemical analysis. Nyquist plots exhibited a high frequency depressed semicircle followed by a straight line portion (Warburg diffusion tail) in the low-frequency region. The impedance data were interpreted according to two suitable equivalent circuits. The kinetics of dissolved O₂ reduction and hydrogen evolution reactions on copper surface were also studied in O₂-saturated 0.50 M H₂SO₄ solutions using polarization measurements combined with the rotating disc electrode (RDE). The Koutecky-Levich plot indicated that the dissolved O₂ reduction at the copper electrode was an apparent 4-electron process.     

Effect of the cerium (III) chloride heptahydrate on the corrosion inhibition of aluminum alloy

In the present work, the corrosion protection of aluminum alloy AA2024-T3 has been studied in NaCl solution, with and without the addition of cerium (III) chloride heptahydrate. The corrosion inhibitor efficiency after immersion into 10 mM NaCl, with or without 3 mM of CeCl₃·7H₂O at 20°C, 40°C, and 60°C was investigated. The performed quantitative tests include electrochemical techniques, such as the method of quasipotentiostatic polarization (Tafel extrapolation), cyclic polarization, and electrochemical impedance s pectroscopy to determine corrosion rate (v_corr), inhibition efficiency (η %), protective ability (γ), degree of coverage (ϑ), and pitting nucleation resistance. The samples were analyzed with scanning electron microscopy and energy dispersive X-ray analysis to evaluate and characterize the precipitates formed on the surface of aluminum samples and to determine dominant type of corrosion. The formation of Ce³⁺ precipitates occurred on cathodic intermetallic sites and the surface, in general, resulting in improved corrosion resistance. Tested cerium (III) chloride heptahydrate proved to be an effective inorganic corrosion inhibitor for AA2024-T3 in chloride solution, which, by the action of cerium ions, reduced corrosion on the surface of the studied aluminum alloy.     

On electrochemical techniques for interface inhibitor research

The electrochemical behavior related to different modes of inhibition effect is discussed for interface inhibitors. The action coefficients of an inhibitor on the anodic and cathodic reactions (f_a and f_c, respectively) of a corrosion process are defined. An equation is deduced which denotes that if the inhibition effect is caused by geometrically blocking the surface of metal electrode by adsorbed inhibitive species, the corrosion potential in the inhibitor-containing solution will be nearly equal to that in the solution without the inhibitor. In this case the inhibition efficiency (η) equals the coverage (Θ) of the adsorbed species and can be estimated by polarization resistance (R_p) measurements. In addition, the plot of η vs the “relative coverage” (μ) estimated from interfacial capacitance measurements will be a straight line through the original point of the coordinate. If the inhibition is not due to the geometric blocking effect, which can be judged by the noticeable shift of corrosion potential as the inhibitor is added into the solution, then η cannot be estimated by R_p and does not equal Θ. Instead, transfer resistance (R_t) can always be employed to estimate inhibition efficiency whatever the mode of the inhibition effect. It is argued that theoretically no Tafelian straight lines can be measured in solutions with interface inhibitors unless Θ is independent of the electrode potential E or f_a and f_c of the inhibitor change linearly with E. Equations of faradaic admittance at the corrosion potential in inhibitor-containing solution for different modes of inhibition effect are deduced. In addition to the estimation of R_t, R_p and interfacial capacitance, information on the adsorption of the inhibitive species can also be gathered by EIS measurement. In the case of the geometric blocking effect, the EIS display in the inhibitor-containing solution will be similar to that in the black solution when η is low, while a single capacitive loop will display when η is high. If the inhibition is not due to the geometric blocking effect, two time constants will be involved in the EIS display measured in the inhibitive-containing solution no matter what the displays of EIS in the blank solution are, and in this case the effect of E on Θ can be predicted based on the EIS and polarization curve measurements.     

Synergistic effect of polyaspartic acid and iodide ion on corrosion inhibition of mild steel in H2SO4

The inhibition effect of polyaspartic acid (PASP) and its synergistic effect with KI on mild steel corrosion in 0.5 M H₂SO₄ solution are studied by weight loss and electrochemical methods. The inhibition efficiency increases with the concentration of PASP and increases further with the presence of 1 mM KI. Result of the zero charge potential measurement shows that iodide ion promotes the film formation of PASP greatly. The mild steel surfaces after immersion test were analyzed using scanning electron microscopy and X-ray photoelectron spectroscopy. An adsorption model is proposed to elucidate the synergistic mechanism of synergistic effect.     

Inhibition effect and theoretical investigation of dicarboxylic acid derivatives as corrosion inhibitor for aluminium alloy

The corrosion inhibition ability of l -malic acid (MaA) and l -aspartate acid (AsA) against corrosion of the AA5052 alloy in 4 M sodium hydroxide–ethylene glycol solution is investigated. The presence of MaA and AsA in corrosion solution shows a remarkable inhibition of hydrogen evolution of the AA5052 alloy. AsA has the better inhibition effect for the self-corrosion of the AA5052 alloy and its max protection efficiency is 82.1%. This shows that the Mulliken charges of the nitrogen atom of the amine group on the AsA is lower than the Mulliken charge of the oxygen atom of the hydroxyl group on the MaA; the total Mulliken charge of AsA is lower than MaA, and AsA has a higher E_HOMO and a lower energy gap, ΔN. The amine group and carboxyl group on the AsA is easier to coordinate with Al³⁺ ions to form a stable complex.     

Sodium molybdate as a corrosion inhibitor for aluminium in H3PO4 solution

The inhibition effect of sodium molybdate (Na₂MoO₄) on the corrosion of aluminium in 1.0 M H₃PO₄ solution was studied by weight loss, potentiodynamic polarisation curves and electrochemical impedance spectroscopy (EIS) methods. The results show that Na₂MoO₄ is a good inhibitor, and the inhibition efficiency obtained by three methods is higher than 84% at 20 mM. The adsorption of Na₂MoO₄ obeys Freundlich isotherm at lower concentrations (1–7 mM), while Langmuir isotherm at higher concentrations (7–20 mM). Polarisation curves indicate that Na₂MoO₄ acts as an anodic inhibitor. EIS spectra exhibit three loops (two capacitive loops and one inductive loop).     

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.     

Inhibitory effect of some amino acids on corrosion of Pb-Ca-Sn alloy in sulfuric acid solution

The present article describes the inhibition effect of amino acids cysteine (Cys), methionine (Met) and alanine (Ala), towards the corrosion of lead-alloy (Pb-Ca-Sn) in H₂SO₄ solution by potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), weight loss measurement and scanning electron microscopy (SEM) methods. The influence of inhibitor concentration, temperature and time on inhibitory behavior of the amino acids was investigated. The corrosion data including corrosion current density (I_corr), corrosion potential (E_corr) and charge transfer resistance (R_ct) were determined from Tafel plots and EIS. Recording impedance spectra showed that the charge transfer resistance is increased by increasing adsorption time. The SEM micrographs revealed that the corroded surface area is decreased in the presence of amino acids. Meanwhile, the inhibition efficiency (IE) was found to be depending on the type of amino acid and its concentration. The IE for 0.1 M Cys in 0.5 M H₂SO₄ is greater than 96%. Adsorption isotherms were fitted by Langmuir isotherm.     

An innovative specimen configuration for the study of Mg corrosion

Based on an analysis of galvanic corrosion research, the research reported herein was formulated to examine the measurement of polarisation curves for Mg to develop a methodology whereby reliable polarisation curves can be measured for Mg. Cathodic polarisation curves were measured for high purity Mg in 3.5% NaCl saturated with Mg(OH)₂ using three specimen types: (i) mounted specimens, (ii) specimens hung by fishing line and (iii) plug-in specimens. Cathodic polarisation curves were evaluated to yield the corrosion current density i_corr and the corresponding corrosion rate P_i, which was compared with the corrosion rate evaluated from hydrogen evolution measurements, P_H, and the corrosion rate evaluated by weight loss measurements, P_W. Mounted specimens produced values of corrosion rate, P_i, three times larger than values of corrosion rate, P_i, for plug-in specimens, attributed to crevice corrosion in the mounted specimens. Crevice corrosion in Mg is totally unexpected from prior research. The plug-in specimen configuration was designed to have no crevice and to allow simultaneous measurement of P_H and P_i; P_i was consistently less than P_H and indicated an apparent valence for Mg of 1.45 in support of the Mg corrosion mechanism involving the uni-positive Mg⁺ ion. The plug-in specimen has advantages for the study of Mg corrosion.     

A novel Schiff base-based cationic gemini surfactants: Synthesis and effect on corrosion inhibition of carbon steel in hydrochloric acid solution

The corrosion inhibition characteristics of the synthesized cationic gemini surfactants, namely bis(p-(N,N,N-decyldimethylammonium bromide)benzylidene thiourea (10-S-10), bis(p-(N,N,N-dodecyldimethylammonium bromide)benzylidene thiourea (12-S-12) and bis(p-(N,N,N-tetradecyldimethylammonium bromide)benzylidene thiourea (14-S-14) on the carbon steel corrosion in 1 M hydrochloric acid have been investigated at 25 °C by weight loss, potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) techniques. The inhibition efficiencies obtained from all methods employed are in good agreement with each other. The obtained results show that compound 14-S-14 is the best inhibitor with an efficiency of 97.75% at 5 × 10⁻³ M additive concentration. Generally, the inhibition efficiency increased with increase of the inhibitor concentration. Changes in impedance parameters (charge transfer resistance, R_ct, and double-layer capacitance, C_dl) were indicative of adsorption of 14-S-14 on the metal surface, leading to the formation of a protective film. The potentiodynamic polarization measurements indicated that the inhibitors are of mixed type. The adsorption of the inhibitors on the carbon steel surface in the acid solution was found to obey Langmuir’s adsorption isotherm. The free energy of adsorption processes were calculated and discussed. The surface parameters of each synthesized surfactant were calculated from its surface tension including the critical micelle concentration (CMC), maximum surface excess (Γ_max) and the minimum surface area (A_min). The free energies of micellization (ΔG^o_mic) were calculated. The surface morphology of carbon steel sample was investigated by scanning electron microscopy (SEM).