Assessing the corrosion protection property of coatings loaded with corrosion inhibitors using the real-time atmospheric corrosion monitoring technique

The atmospheric corrosion monitoring(ACM)technique has been widely employed to track the real-time corrosion behavior of metal materials.However,limited studies have applied ACM to the corrosion protection properties of organic coatings.This study compared a bare epoxy coating with one containing zinc phosphate corrosion inhibitors,both applied on ACM sensors,to observe their corrosion protection properties over time.Coatings with artificial damage via scratches were exposed to immersion and alternating dry and wet environments,which allowed for monitoring galvanic corrosion currents in real-time.Throughout the corrosion tests,the ACM currents of the zinc phosphate/epoxy coating were considerably lower than those of the blank epoxy coating.The trend in ACM current variations closely matched the results obtained from regular electrochemical tests and surface analysis.This alignment highlights the potential of the ACM technique in evaluating the corrosion protection capabilities of organic coatings.Compared with the blank epoxy coating,the zinc phosphate/epoxy coating showed much-decreased ACM current values that confirmed the effective inhibition of zinc phosphate against steel corrosion beneath the damaged coating.

Influence of Mineral Admixtures on Corrosion of Steel Rebar in Concrete

The effects of several mineral admixtures such as silica fume,granulated ground blast furnace slag and fly ash at different replacement ratio instead of Portland cement on the corrosion of steel reinforced concrete were investigated.By measuring the rebar anode polarization curve,permeability of concrete,mass loss of steel rebar and the amount of chloride ions and hydroxide in mortar,the corrosion resistance of steel embedded in fresh mortar incorporated of salt and different mineral admixtures were evaluated respectively.The results show that most mineral admixture can not improve corrosion resistance of concrete at early ages.However,in the long term the addition of mineral admixtures can decrease obviously the permeability of concrete and free chloride content in the pore solution of concrete as well as effectively improve the protection ability of passive film of steel rebar.

Effects of chitosan inhibitor on the electrochemical corrosion behavior of 2205 duplex stainless steel

The effects of chitosan inhibitor on the corrosion behavior of 2205 duplex stainless steel were studied by electrochemical measurements, immersion tests, and stereology microscopy. The influences of immersion time, temperature, and chitosan concentration on the corrosion inhibition performance of chitosan were investigated. The optimum parameters of water-soluble chitosan on the corrosion inhibition performance of 2205 duplex stainless steel were also determined. The water-soluble chitosan showed excellent corrosion inhibition performance on the 2205 duplex stainless steel. Polarization curves demonstrated that chitosan acted as a mixed-type inhibitor. When the stainless steel specimen was immersed in the 0.2 g/L chitosan solution for 4 h, a dense and uniform adsorption film covered the sample surface and the inhibition efficiency(IE) reached its maximum value. Moreover, temperature was found to strongly influence the corrosion inhibition of chitosan; the inhibition efficiency gradually decreased with increasing temperature. The 2205 duplex stainless steel specimen immersed in 0.4 g/L water-soluble chitosan at 30°C displayed the best corrosion inhibition among the investigated specimens. Moreover, chitosan decreased the corrosion rate of the 2205 duplex stainless steel in an FeCl_3 solution.

Electrochemical and analytical characterization of three corrosion inhibitors of steel in simulated concrete pore solutions

Corrosion inhibitors for steel, such as sodium phosphate （Na3PO4）, sodium nitrite （NaNO2）, and benzotriazole （BTA）, in simulated concrete pore solutions （saturated Ca（OH）2） were investigated. Corrosion behaviors of steel in different solutions were studied by means of corrosion potential （Ecorr）, linear polarization resistance （LPR）, electrochemical impedance spectroscopy （EIS）, and potentiodynamic polarization （PDP）. A field emission scanning electron microscope （FESEM） equipped with energy dispersive X-ray analysis （EDXA） was used for observing the microstructures and morphology of corrosion products of steel. The results indicate that, compared with the commonly used nitrite-based inhibitors, Na3PO4 is not a good inhibitor, while BTA may be a potentially effective inhibitor to prevent steel from corrosion in simulated concrete pore solutions.

Effectiveness of inhibitors in increasing chloride threshold value for steel corrosion

This investigation was aimed at evaluating the effectiveness of corrosion inhibitors in increasing the chloride threshold value for steel corrosion. Three types of corrosion inhibitors, calcium nitrite （Ca（NO2）2）, zinc oxide （ZnO）, and N,N＇-dimethylaminoethanol （DMEA）, which respectively represented the anodic inhibitor, cathodic inhibitor, and mixed inhibitor, were chosen. The experiment was carried out in a saturated calcium hydroxide （Ca（OH）2） solution to simulate the electrolytic environment of concrete. The inhibitors were initially mixed at different levels, and then chloride ions were gradually added into the solution in several steps. The open-circuit potential （Ecorr） and corrosion current density （lcorr） determined by electrochemical impedance spectra （EIS） were used to identify the initiation of active corrosion, thereby determining the chloride threshold value. It was found that although all the inhibitors were effective in decreasing the corrosion rate of steel reinforcement, they had a marginal effect on increasing the chloride threshold value.

Adsorption isotherm mechanism of amino organic compounds as mild steel corrosion inhibitors by electrochemical measurement method

The inhibition ability of 4-amino-5-phenyl-4H-1, 2, 4-trizole-3-thiol （APTT）, ethylenediaminetetra-acetic acid （EDTA） and thiourea （TU） for mild steel corrosion in 1.0 moFL HC1 solution at 30 ℃ was investigated. Tafel polarization and electrochemical impedance spectroscopy （EIS） were used to investigate the influence of these organic compounds as corrosion inhibitors of mild steel in 1.0 mol/L HC1 solution at 30 ℃. The inhibition mechanism was discussed in terms of Langrnuir isotherm model. Results obtained from Tafel polarization and impedance measurements are in a good agreement. The inhibition efficiency increases with the increase of the inhibitor concentration. The adsorption of the inhibitors on the mild steel surface follows Langmuir adsorption isotherm and the free energy of adsorption AGads indicates that the adsorption of APTT, EDTA, and TU molecules is a spontaneous process and a typical chemisorption.

Red tetrazolium as an effective inhibitor for the corrosion of cold rolled steel in 7.0 mol·L^(-1) H_2SO_4 solution

The corrosion inhibition of cold rolled steel(CRS) in 7.0 mol·L^(-1) H_2 SO_4 solution by red tetrazolium(RTZ) was carefully investigated using both experimental procedures and theoretical techniques. The results show that RTZ acts as an effective inhibitor for the corrosion of CRS in 7.0 mol·L^(-1) H_2SO_4, and the maximum inhibition efficiency is higher than 95% with a RTZ concentration of 2.0 mmol·L^(-1). The adsorption of RTZ on CRS surface follows Langmuir isotherm. RTZ effectively retards both cathodic and anodic reactions, and acts as a mixed-type inhibitor. EIS exhibits two capacitive loops, and their resistances increase drastically in the presence of RTZ. SEM and AFM confirm that the addition of RTZ could significantly retard the corrosion of CRS surface. A series of characterizations like FTIR, RS, XRD and XPS reveal that the corrosion CRS surface is composed of the corrosion products of iron sulfates, iron oxides and iron hydroxide, as well as inhibitor. Theoretical results of quantum chemical calculation and molecular dynamics(MD) indicate that the adsorption center of RTZ+(organic cationic part of RTZ) mainly relies on its tetrazole ring,and the adsorption of RTZ+on Fe(001) surface is in a nearly flat orientation mode.

Anticorrosion Performance of Carbon Steel in 55% LiBr Solution Containing PMA/SbBr_3 Inhibitor

The anticorrosion performance of carbon steel in 55 % LiBr solution containing PMA/SbBr3 inhibitor was studied by weight-loss tests, electrochemical measurements and surface analysis. In 55 %LiBr＋PMA/SbBr3 solution, corrosion rates of carbon steel at 145 ℃, 175℃, 190℃ and 240℃ are 18.32μm·a^-1 , 27.68μm·a^-1, 53.58μm·a^-1 and 73. 78μm·a^-1 , respectively. PMA/SbBr3 inhibitor may inhibit the corrosion of carbon steel in 55% LiBr solution effectively. Especially, it shows an excellent corrosion inhibition performance at high temperature. Both anodic and cathodic reactions of carbon steel may be inhibited by PMA/SbBr3 inhibitor, so it may be classified as mixed inhibitor. In 55%LiBr＋PMA/SbBr3 solution, the apparent activation energy of the corrosion reaction of carbon steel is 29. 61 kJ·mol^-1. The corrosion inhibition mechanism of PMA/SbBr3 is suggested as follows： PMA has the effect of inhibiting hydrogen evolution and a strong oxidizing property; Sb^3＋ also exhibits oxidizing properties, and can exist stably with PMA in LiBr solutions; the passive film comprising Fe2O3 and antimony formed on carbon steel surface may prevent Brfrom diffusing into the metal surface due to the synergistic effect of PMA and Sb^3＋ ; As a result, the anticorrosion performance of carbon steel may be improved by PMA/SbBr3 inhibitor in 55% LiBr solution.

Synergic Mechanism of an Organic Corrosion Inhibitor for Preventing Carbon Steel Corrosion in Chloride Solution

The inhibition effect of dimethylethanolamine（DMEA） and its composite with carboxylic acid was studied with the electrochemical tests. The experimental results indicate that DMEA is not a good inhibitor but the composite of DMEA with caprylic acid exhibits excellent inhibiting efficiency. The synergic mechanism of the organic corrosion inhibitors（OCIs） was studied with quantum chemical calculations. It is found that the DMEA forms a quaternary ammonium salt with the proton in carboxylic acid, and a cyclic complex formed between the salt and Fe may be responsible for the enhancement of inhibiting efficiency. The possible hydrogen bond formed between DMEA and carboxylic acid is not enough for the inhibiting effect. This work is helpful to proposing theoretical interpretation as well as developing a functional organic inhibitor to improve the durability of reinforced concrete contaminated with chloride.

Benevolent behavior of Kleinia grandiflora leaf extract as a green corrosion inhibitor for mild steel in sulfuric acid solution

The ethanolic extract of Kleinia grandiflora leaves was characterized and tested for its potential anticorrosion properties on mild steel in 1 M H2SO4 medium using mass-loss analysis, potentiodynamic polarization measurements, electrochemical impedance spectroscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy, UV–visible spectroscopy, and X-ray diffraction analysis. The effect of temperature on the corrosion behavior of mild steel was studied in the range of 308 to 328 K. The inhibition efficiency was observed to increase with increasing concentration of the extract. Polarization curves revealed that the Kleinia grandiflora leaf extract is a mixed inhibitor. Impedance diagrams revealed that an increase of Kleinia grandiflora leaf extract concentration increased the charge transfer resistance and decreased the double-layer capacitance. The adsorption process obeys Langmuir＇s model, with a standard free energy of adsorption（ΔGads） of-18.62 k J/mol. The obtained results indicate that the Kleinia grandiflora leaf extract can serve as an effective inhibitor for the corrosion of mild steel in a sulfuric acid medium.

1-Hydroxyethylidene-1,1-diphosphonic Acid (HEDP) as a Corrosion Inhibitor of AISI 304 Stainless Steel in a Medium Containing Chloride and Sulfide Ions in the Presence of Different Metallic Cations

The novelty of this paper is the analysis in a medium containing sulfide ion due to the generation of this ion in petroleum industries, in the refining stage (the sulfide ion is also present on the produced water). The performance of 1-hydroxyethylidene-1,1-diphosphonic acid inhibitor (HEDP) was investigated by potentiodynamic polarization, electrochemical impedance spectroscopy, and weight loss measurements in a dissolution of AISI 304 stainless steel immersed in a solution containing chloride and sulfide ions. The protection of the stainless was increased with the addition of divalent cations (Ca2+, Zn2+, and Mg2+). Potentiodynamic polarization studies have shown that the inhibitor alone has anodic protection, but the addition of Ca2+ (10 mg·L-1) favors the cathodic protection, and the addition of Zn2+ (20 mg·L-1) and Mg2+ (10 mg·L-1) mixed-type is observed. Electrochemical impedance spectroscopy was performed at three distinct potentials: -0.3 [V vs. SCE], Ecorr [V vs. SCE], and 0.1 [V vs. SCE]. This revealed that calcium is responsible for favoring the formation of the film and the other elements (zinc and magnesium) favor the stabilization of the protective film. Scanning electron microscopy analysis revealed that the addition of cations provided the adsorption of HEDP on the metal surface. Weight loss results showed that the presence of zinc in a solution containing HEDP favored greater inhibitor efficiency (Zn2+ ηm = 85.2% and for Mg2+ ηm = 70.4%).

Performance Evaluation of a Novel and Effective Water-Soluble Aldehydes as Corrosion Inhibitor for Carbon Steel in Aggressive Hydrochloric Medium

A novel and effective water-soluble aldehydes(β-HA)as corrosion inhibitor was synthesized for N80 steel corro-sion in 15%HCl solution,and the corrosion inhibition performance was evaluated by using weight loss,electro-chemical measurements,scanning electron microscope(SEM),quantum chemical calculation and molecular dynamics simulation(MDS).The results show that synthesizedβ-HA showed excellent corrosion performance compared with MHB and PE for carbon steel in 15%HCl solution compared with MHB and PE,and the inhibi-tion efficiency increased with increasing concentration of the inhibitor.The inhibition efficiency of β-HA at 8 mmol/L reached the maximum value 94.08%.The inhibitor acted as mixed-type inhibitor via blocking both the anodic and cathodic reaction.The adsorption of inhibitors on N80 steel surface obeyed Langmuir adsorption isotherm,and the process contained chemisorption and physisorption.TheΔG ads of β-HA was−28.81 kJ·mol^(-1)der the standard atmospheric pressure.Moreover,the theoretical calculation parameters revealed stronger combination and higher interaction energy for inhibitor β-HA comparing with MHB and PE,further demonstrat-ing the correlation between the theoretical and experimental results.

Prevention of Q235 Steel Corrosion using Waterborne Rust Inhibitor

Sorbitol,triethanolamine,sodium benzoate,boric acid,and sodium carbonate were mixed to prepare a waterborne rust inhibitor.A temperature and humidity accelerated corrosion test was applied to investigate the corrosion behaviour of waterborne rust inhibitor coated Q235 steel and original Q235 steel,which was carried out in a temperature and humidity test chamber(WSHW-1000)at a temperature of 80℃and humidity of 95%.Compared with the original Q235,waterborne rust inhibitor coated Q235 has better resistance to corrosion in hot and humid ambient conditions.Electrochemical impedance spectroscopy and potentiodynamic polarization were measured with a three-electrode cell in 3.5%NaCl aqueous solution on a CHI760E potentiostat/galvanostat.Molecular dynamics was simulated to verify the synergistic corrosion inhibitory mechanism of sodium carbonate and triethanolamine.The test shows that the prepared waterborne rust inhibitor can reduce the tendency of Q235 to corrosion and can also effectively reduce the corrosion rate.

Effect of Calcium Nitrate and Sodium Nitrite on the Rebar Corrosion of Medium Carbon Steel in Seawater and Cassava Fluid

Inhibitors are regularly used as one of the principal prevention and control techniques in reinforcement corrosion. Hence this study investigates the effect of calcium nitrate and sodium nitrite inhibitors on the rebar corrosion of medium carbon steel in seawater and cassava fluid with a view to determining inhibitive potentials of the different inhibitors in the two media. Gravimetric and voltametric techniques were employed in this study and a total of forty-five corrosion coupons of different dimensions were produced. Forty coupons were used for gravimetric analysis and the remaining five for corrosion potentials measurements. Eight of the samples were used as control;while other eight samples each were admixed with calcium nitrate and sodium nitrite in concrete cubes. It was later immersed in seawater and cassava fluid for a total duration of 32 days and the measurements were taken at the interval of 4 days in order to determine the corrosion rates in mils per year (mmpy). Two controls and admixed samples each were later immersed in seawater and cassava fluid, respectively, for durations of 32 days to determine the corrosion potentials using a voltmeter and a Copper-Copper Sulphate Electrode (Cu/CuSO4). The pH of each medium was measured throughout the period of exposure. The results obtained expressed that all the samples except the control samples, displayed some degree of inhibition. The inhibition levels for the admixed samples in seawater were higher compared with those in cassava fluid. Inhibition efficiencies for various inhibitors followed different trends in different environment. The inhibition efficiencies for calcium nitrate in cassava fluid and seawater were 26.81% and 64.85% respectively. The study concluded that inorganic inhibitors were effective in inhibiting corrosion in cyanide and chloride contaminated concrete cubes.

Effect of Toluene and Dioctylphthalate on the Rebar Corrosion of Medium Carbon Steel in Seawater and Cassava Fluid

Chemical mitigation is regularly used as one of the principal prevention and control techniques in reinforcement corrosion. Hence this study presents the effect of toluene and dioctylphthalate on the rebar corrosion of medium carbon steel in seawater and cassava fluid with a view to determining inhibitive potentials of the different inhibitors in the two media. Gravimetric and voltametric techniques were employed in this study and a total of forty-five corrosion coupons of different dimensions were produced. Forty coupons were used for gravimetry and the remaining five for corrosion potentials measurements. Eight of the samples were used as control;while other eight samples were admixed with dioctylphthalate and toluene in concrete cubes. It was later immersed in seawater and cassava fluid for a total duration of 32 days and the measurements were taken at interval of 4 days in order to determine the corrosion rates in mils per year (mmpy). Two controls and admixed samples were later immersed in seawater and cassava fluid, respectively, for durations of thirty-two days to determine the corrosion potentials using a voltmeter and a Copper-Copper Sulphate Electrode (Cu/CuSO4). The pH of each medium was also measured throughout the period of exposure. The results obtained showed that all the samples except the control samples, displayed some degree of inhibition. The inhibition levels for the admixed samples in seawater were on the higher side compared with those in cassava fluid. The inhibition efficiencies for different inhibitors followed different trends in different environment. The inhibition efficiencies for toluene in cassava fluid and seawater were 21.64% and 45.78% respectively. The study concluded that organic inhibitors were effective in inhibiting corrosion in cyanide and chloride contaminated concrete cubes.

Surface Analysis of Carbon Steel Protected from Corrosion by a New Ternary Inhibitor Formulation Containing Phosphonated Glycine, Zn²⁺and Citrate

Studies on surface analysis of carbon steel protected from corrosion in low chloride and nearly neutral aqueous environment by a synergistic mixture containing N,N-bis(phosphonomethyl) glycine (BPMG), zinc ions and citrate ions are presented. The effect of addition of citrate to the binary system, BPMG-Zn2+, is quite significant and is well explored through various studies. The surface protective nature is maintained in the pH range 5 - 9. Potentiodynamic polarization studies inferred that the ternary inhibitor is a mixed inhibitor. Impedance studies of the metal/solution interface indicated that the surface film is highly protective against the corrosion of carbon steel in the chosen environment. X-ray photoelectron spectroscopic (XPS) analysis of the surface film showed the presence of the elements namely iron, phosphorus, nitrogen, carbon, oxygen and zinc. Deconvolution spectra of these elements in the surface film inferred the presence of oxides/hydroxides of iron(III), Zn(OH)2 and [Fe(III), Zn(II)-BPMG-citrate] heteropolynuclear multiligand complex. This inference is further supported by the reflection absorption Fourier transform infrared spectrum of the surface film. Analysis by scanning electron microscopy (SEM) is presented for both the corroded and protected metal surfaces. Based on all these results, a plausible mechanism of corrosion inhibition is proposed.

Study on the Corrosion inhibitor and Fog Suppressor for Chemical Pickling of Iron and Steel

A new type of corrosion inhibitor and fog suppressor composed of Nitrogen-containing alkaloid,water-soluble butadiene lower polymer, and inorganic electrolyte has been investigated by gravimetric and electrochemical method. Effects or this chemicals on pickling rate and hydrogen penetration into iron and steel material in 50～150 g/L HCI or/and H2SO4 solutions at 20～70℃ temperature were examined. The amount of acid fog escaping from the surface of air-liquid was determined by chemical titration. The results indicate that the efficiency of inhibition and suppression depends on film properties by which mean a barrier film on the interface of bare mild steel/solution or an unsolvable liquid membrane as hydrophibic effect.In present work the film-forming mechanism by in situ and chemistry-mechanics effect is also discussed.

Evaluation of Propargyl Alcohol as a Corrosion Inhibitor for Duplex Stainless Steel in Hydrochloric Acid

ASTM A182 F51 duplex stainless steel with a 50:50 ratio of austenite to ferrite microstructure is a material used in mechanical engineering.Its uses include the manufacturing of equipment and components subject to acidification or acid stimulation for oil and gas industries.During acid stimulation or acidification,hydrochloric acid(HCl)solution with concentrations ranging from 5%to 28%(by volume)is injected into the limestone(CaCO3)and dolomite(CaCO3·MgCO3)reservoir rock to restore permeability and consequently increase oil well productivity.Therefore,it is important to use a corrosion inhibitor,such as propargyl alcohol,to prevent or inhibit the aggressive attack of HCl on duplex stainless steel.The present study evaluates the corrosion resistance of ASTM A182 F51 stainless steel using gravimetric(mass loss)and electrochemical(polarization)tests.Studies were completed with and without the addition of 500 and 1,000 mg/L propargyl alcohol in HCl solutions with concentrations of 10%and 15%(by volume)at temperatures of 25,40 and 55°C.The good protection by propargyl alcohol of duplex steel immersed in HCl is observed.

Novel Corrosion Inhibitors for Carbon Steel Alloy in Acidic Medium of 1N HCl Synthesized from Graphene Oxide

In this study, two nano-derivatives from nano-Graphene oxide (GO) were synthesized. Regarding to GON and GOS by reaction GO with 2-amino ethanol and 2-marcapto ethanol respectively, the GO, GON, GOS were characterized by FTIR, XRD and FSEM. Evaluation prepared compound to inhibitors corrosion for Carbon steel in acidic media at (1 - 6 ppm) concentration and different temperature 298, 308, 318, 328 K. The electrochemical technique used Tafel plot to measure the efficiency of inhibitor. It was observed that the corrosion rate and charge transfer of the carbon steel for the inhibitor increase with increase of temperature and decrease with increase of the inhibitor concentration in the same temperature. The GON had inhibition efficiency reached 96.96% for the 6 ppm concentration at 298 K.