Anticorrosion Activity of 8-Quinoline Sulphonyl Chloride on Mild Steel in 1 M HCl Solution

Ganapathi Sundaram, R.; Sundaravadivelu, M.

doi:https://doi.org/10.1155/2016/8095206

Journal of Metallurgy

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Research Article | Open Access

Volume 2016 | Article ID 8095206 | https://doi.org/10.1155/2016/8095206

Anticorrosion Activity of 8-Quinoline Sulphonyl Chloride on Mild Steel in 1 M HCl Solution

R. Ganapathi Sundaram¹and M. Sundaravadivelu¹

Academic Editor: Menahem Bamberger

Received20 Oct 2015

Revised31 Jan 2016

Accepted01 Feb 2016

Published29 Feb 2016

Abstract

An anticorrosion activity of 8-quinoline sulphonyl chloride (8-QSC) on mild steel in 1 M HCl solution was studied by weight loss (WL) method and electrochemical methods, namely, electrochemical impedance spectroscopy (EIS), Tafel polarization (TP), and linear polarization resistance (LPR). Results obtained from WL method, EIS, TP, and LPR, showed that 8-QSC is a good corrosion inhibitor for mild steel in 1 M HCl solution. The results indicated that the inhibition efficiency and extent of surface coverage were increased with increase in inhibitor concentration and decrease in the corrosion rate. This is due to the formation of protective film on the surface of mild steel. Adsorption of 8-QSC on the mild steel surface was found to obey the Langmuir adsorption isotherm. A Tafel plot indicates that the used inhibitor behaves predominantly as cathodic type. The surface morphology of the mild steel was studied by Scanning Electron Microscopy (SEM) and Energy Dispersive X-Ray (EDX) Spectroscopy techniques. All the methods give the same order of inhibition efficiencies.

1. Introduction

Corrosion is the destruction of metals and alloys by chemical interaction with their environment. The word corrosion is sometimes use for the degradation of plastics, concrete, and wood but generally refers to active metals. Active metals like mild steel, Zn, Al, and Cu are employed in various industries for fabrication purposes due to their low cost and easy availability, where surfaces are rapidly damaged in acid media [1, 2]. In order to reduce the damage (corrosion) of active metals, a number of techniques like metallic coatings, anodic protection, cathodic protection, inhibitors, and so forth, have been applied. Among the numerous anticorrosion measures, the use of organic inhibitors is one of the most economical and practical methods for protection of metals and alloys against corrosion [3–5]. The organic compounds containing nitrogen, oxygen, sulphur, and phosphorous, heterocyclic compounds with a polar functional group, and conjugated double bonded or triple bonded compounds have been widely used as acid inhibitors [6–8]. Heterocyclic compounds, such as pyridine, pyridine derivatives, pyrazole, triazole, tetrazole, and benzothiazole derivatives, have been reported and they show better inhibition efficiency for metals especially mild steel in different media [6, 9]. The existing data show that most of the organic inhibitors act by adsorption on the metal and alloys surface [10]. Adsorption of an inhibitor by a metal surface depends on the nature and surface charge on the metal, the mode of adsorption, and the electronic structure of the inhibitor. The inhibitor molecules get bonded to the mild steel surface by chemisorption, physisorption, or complexation with the polar groups acting as the reactive centers in the molecules [11].

In the present work, we have studied an anticorrosion activity of various concentrations of 8-QSC on mild steel in 1 M HCl solution. From this work, the rate of corrosion was decreased with increasing the inhibitor concentration, Bbecause the studied inhibitor molecule contains a number of heteroatoms like oxygen, sulphur, and benzene ring with active centers like nitrogen and aromatic electrons.

2. Experimental Part

2.1. Materials Preparation

The material used in the present work is mild steel with chemical composition of (% wt) 0.104% C, 0.58% Mn, 0.035% P, 0.026% S, and the remaining Fe, which was mechanically cut into 3.5 × 1.5 × 0.2 cm dimensions for weight loss measurements and 1.0 × 1.0 × 0.2 cm dimensions for SEM studies. For an electrochemical measurement, 1.0 cm² surface area of the material was exposed to the corrosive medium and the rest was being covered by epoxy resin. The surfaces of all the specimens (weight loss, SEM, and electrochemical measurements) were polished with different grades of emery papers like 1/0, 2/0, 3/0, 4/0, 5/0, 6/0, and 7/0, then subsequent cleaned with AR grade acetone, and finally dried.

2.2. Inhibitor Preparation

The heterocyclic compound 8-QSC was received from SIGMA-ALDRICH and used as corrosion inhibitor. The molecular structure and the optimized structure of the studied inhibitor are given in Figure 1. The test solution 1 M HCl was prepared using analytical grade 37% HCl and bidistilled water. The stock solution of 8-QSC was made in 1 M HCl by dissolving 8-QSC in ethanol (1 gm/50 mL) and it is used for all experimental purposes. The various concentrations of inhibitor (50–300 ppm) solution and without the presence of inhibitor solution (1 M HCl) are taken as blank for comparison.

2.3. Weight Loss Measurements

The weight loss measurements were done according to the standard method as described earlier [12]. In this method, previously polished, degreased, and weighed mild steel specimens were immersed in 100 mL aerated test solutions in the absence and presence of various concentrations of inhibitor and various immersion times (1, 3, and 6 hrs) at room temperature. After the immersion hrs, the specimens were carefully washed in acetone and weighed accurately. Duplicate experiments were also carried out on the same condition and the mean value of the weight loss is reported.

From this measurement, the corrosion rate was calculated by using the following equation: where is the mass of the test piece before corrosion, is the mass of the test piece after corrosion, is the total surface area of the test piece, is the exposure time, and is the weight loss of test piece specimens. The surface coverage () and inhibition efficiency (IE%) was determined by the following equations:where is the rate of corrosion in the absence of inhibitor and is the rate of corrosion in the presence of inhibitor, respectively.

2.4. Electrochemical Measurements

All the electrochemical measurements’ potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) were carried out using CH-Electrochemical analyzer model 760D with CHI 760D software. For these electrochemical measurements, conventional three-electrode cell systems were used. In this setup, the polished mild steel with 1.0 cm² exposed surface area was used as working electrode, platinum electrode was used as an auxiliary electrode, and saturated calomel electrode was used as reference electrode. Before starting the electrochemical measurements, the working electrode mild steel was allowed to corrode freely with the help of 1 M HCl solution without inhibitor and its open circuit potential (OCP) was recorded as a function of time up to 30 minutes, which was sufficient to attain a stable state [13]. All potentials were measured versus saturated calomel electrode.

EIS measurements were carried out by using ac impedance signal of 0.01 V amplitude for the frequency ranging from 0.1 to 1,0000 Hz. Nyquist and Bode curves were obtained. From the Nyquist curves, the values of , , and of mild steel in the absence and presence of various concentrations of inhibitor in 1 M HCl solution were computed.

The Tafel curves were obtained by changing the electrode potential automatically from −300 to +300 mV versus the open circuit potential at a scan rate of 0.1 mV/s. For the linear polarization resistance measurements, the potential of the electrode was scanned from −0.02 to +0.02 V versus at a scan rate of 0.125 mV/s [14]. All the above electrochemical measurements are repeated two times under the same condition to confirm the accuracy of the data obtained.

2.5. Surface Morphology Measurements

The surface morphology of the mild steel specimens in the absence and the presence of optimum concentration of inhibitor was analyzed using Scanning Electron Microscopy (SEM) and Energy Dispersive X-Ray (EDX) Spectroscopy, analyzing the elements present on the mild steel surface. Both SEM and EDX studies were performed on JEOL/EO JSM-6390 instrument.

3. Results and Discussion

3.1. Weight Loss Measurements

The values of corrosion behavior of mild steel in 1 M HCl solution in the absence and presence of various concentrations of inhibitor from weight loss measurements are given in Table 1 and Figures 2(a) and 2(b). From this study, the inhibition efficiency increases with increase in concentration of the inhibitor. However, increasing the immersion time, the inhibition efficiencies slowly decrease. The maximum efficiency 82.69% is obtained at 300 ppm of inhibitor solution after 3 h of immersion time of mild steel specimens, which explains the effect of protection of metal against corrosion due to the adsorption of studied inhibitor. Figure 2(b) shows that the corrosion rate of mild steel deceases from 14.60 mm y⁻¹ to 5.19 mm y⁻¹ on the addition of 50 ppm to 300 ppm of inhibitor after 3 h of immersion time. The increase in efficiency from 51.30% to 82.69% may be due to the blocking effect of the metal surface by adsorption and film formation mechanisms, which decreases the effective area of corrosion attack [15]. In Figure 2(a), the inhibition efficiency is increasing with inhibitor concentration the maximum efficiency is reached at a concentration of 300 ppm, while further increasing the inhibitor concentration (350 and 400 ppm) does not show any appreciable change in the efficiency. The reason for this study may be that all the active sites of surface of mild steel are completely adsorbed by the inhibitor molecule and there no empty active sites are available for further adsorption. From the weight loss measurements, we have concluded 3 h is the maximum time for inhibition process. The inhibiting performance exhibited by the compound may be due to the presence of protonated form of nitrogen and sulphur atoms, which makes it adsorb and form insoluble protective layer on the surface of mild steel. From these results, it is clear that the studied inhibitor 8-QSC is quickly adsorbed at the corrosion active sites of mild steel surface responsible for anticorrosion activity.

(a)

(b)

3.2. Electrochemical Impedance Spectroscopy (EIS) Measurements

The anticorrosion activity of mild steel in 1 M HCl solution in the absence and presence of various concentrations of inhibitor is investigated by EIS measurements at room temperature. EIS diagrams like Nyquist and Bode plots were obtained and are represented in Figures 3(a) and 3(b). From Figure 3(a), the Nyquist plot, it is clear that the diameter of semicircle increases with increasing the concentrations of inhibitor. The existence of single semicircle showed the single charge transfer process during dissolution which is unaffected by the presence of used inhibitor molecules. It is seen that addition of inhibitor increases the values of charge transfer resistance () and reduces the double-layer capacitance (). The decrease in is attributed to increase in thickness of electronic double layer [16]. The increase in value is due to the formation of protective layer on the surface of mild steel [17]. The values have been estimated from the EIS values using Nyquist plot by the following formula:The values were decreased with an increase in the concentrations of inhibitor. This is due to the formation of protective film on the surface of mild steel by the addition of various concentrations of inhibitor, resulting in an increase in the inhibition efficiency. The EIS parameters such as , , and are given in Table 2. The values of IE% obtained from the charge transfer resistances are calculated according to the following equation:where and indicate the charge transfer resistance values in the presence and absence of inhibitor, respectively.

(a)

(b)

From Figure 3(b), the phase angle at high frequencies gives a general idea of the anticorrosion activity of the inhibitor. The more negative the phase angle, the more capacitive the electrochemical behavior [18]. This is indicative of superior inhibitive behavior of inhibitor at high concentration.

3.3. Potentiodynamic Polarization Measurements

Potentiodynamic polarization measurements were carried out to study the nature of inhibitor, mode of action, and mechanism of the inhibitor reaction. Potentiodynamic polarization curves of mild steel in 1 M HCl solution in the absence and the presence of various concentrations of inhibitor are shown in Figure 4. The important potentiodynamic polarization parameters derived from these (Tafel) curves and are listed in Table 3. The inhibition efficiency (IE%) of the inhibitor values were evaluated from calculated (from Tafel curves using CHI software) corrosion current density () values using the following relationship: where and are the corrosion current density in the absence and presence of inhibitor solution, respectively. Table 3 shows that the corrosion current density () values decrease from 1.894 mA cm⁻² to 0.3850 mA cm⁻² with the addition of optimum concentrations of inhibitor. It clearly indicates values were decreased prominently and IE% increased with increased inhibitor concentration. The decrease of current density is due to the adsorption of inhibitor molecules on mild steel surface to retard the corrosion reaction of electrode with simultaneous replacement of electrolyte solutions at the interface [19]. From this study we observed that, on increasing the inhibitor concentration (50–300 ppm), corrosion potential () values were shifted towards cathodic side (negative side). However, according to Ferreira and others [20, 21], if the displacement of corrosion potential () is greater than 85 mV with respect to the corrosion potential () of the blank solution, the inhibitor can be seen as a cathodic or anodic type. In this study, the maximum displacement was 99 mV cathodically with respect to the blank. This indicates that the studied inhibitor behaves predominantly as cathodic type.

3.4. Linear Polarization Resistance Measurements

The linear polarization resistance () values were derived from the slope of the potential versus current lines. The inhibition efficiencies and linear polarization resistance parameters values are given in Table 4. The inhibition efficiency (IE%) and surface coverage were calculated using the following relationship [14]:where and are the linear polarization resistance values in the presence and absence of inhibitor, respectively. The results obtained from weight loss, EIS, and Tafel polarization method showed good agreement with the results obtained from linear polarization resistance. From Table 4, it is shown there is increasing in the value and inhibition efficiency with increases in the various concentrations of inhibitor.

3.5. Adsorption Isotherm Measurements

Adsorption isotherm gives information about the interaction of the adsorbed molecules (inhibitor) with the electrode (mild steel) surface [22]. Two types of interaction can explain the adsorption of the inhibitors on the surface of mild steel: physisorption and chemisorption [23, 24]. The type of adsorption is mainly based on the molecular structure of the inhibitor, type of the electrolyte, and nature of the metal [25]. The surface coverage is very useful for understanding the adsorption behavior of studied inhibitor. The inhibition efficiency of used inhibitor was studied by chemical (WL) and electrochemical (EIS, Tafel, and LPR) methods, which suggest that the surface coverage was increased with increasing the inhibitor concentration. To explain the adsorption characteristics of 8-QSC, several adsorption isotherms have been tested with the values of all methods (WL, EIS, Tafel, and LPR) and the Langmuir adsorption isotherm model fits the experimental data well. According to Langmuir isotherm, is related to by the following equation: where is the inhibitor concentration (ppm), is the degree of surface coverage, and is the equilibrium constant of the adsorption process.

The values can be calculated from the intercept lines on the axis. This is related to with the following equation: where is the universal gas constant, is the absolute temperature, and 55.5 is the concentration of water in solution in mol L⁻¹ [26]. The calculated values of , , and are given in Table 5. Figure 5 shows the straight line of versus for various concentrations of inhibitor at room temperature. These results show that the linear regression coefficient () and slope are equal to unity, which confirms the adsorption of studied inhibitor on mild steel surface. Generally the calculated standard free energy () values up to −20 kJ mol⁻¹ are consistent with electrostatic interaction between the charged inhibitor molecules and the charged metal surface (physisorption) while those around −40 kJ mol⁻¹ or higher values are associated with chemical interaction or chemisorption as a result of sharing or transfer of electrons from the organic inhibitor molecules to the metal surface to form a coordinate covalent bond [27, 28].

In the present study, the values obtained from weight loss method, EIS method, Tafel method, and LPR method were −17.45, −18.82, −17.90, and −17.53, respectively. The above results confirmed the inhibitor adsorbed on the metal surface via physical adsorption and the adsorption process is always spontaneous.

3.6. Scanning Electron Microscopy Measurements

The surfaces of mild steel were analyzed using Scanning Electron Microscope (SEM) after the immersion of 3 hrs in 1 M HCl solution in the absence and presence of optimum concentration (300 ppm) of inhibitor. The SEM images of polished mild steel, 1 M HCl solution without inhibitor, and 1 M HCl solution with inhibitor are given in Figures 6(a)–6(c). This study clearly indicates that the anticorrosion activity is increased remarkably in the presence of inhibitor.

(a)

(b)

(c)

3.7. Energy Dispersive X-Ray Spectroscopy (EDX) Measurements

The Energy Dispersive X-Ray (EDX) Spectroscopy technique was employed in order to get information about the percentage of atomic composition of the surface of the polished mild steel, in the absence and presence of optimum concentration of inhibitors in 1 M HCl solution. The results of EDX spectra were given in Figures 7(a)–7(c).

(a)

(b)

(c)

The atomic contents (%) of various elements in the polished, corroded, and inhibited mild steel surfaces were analyzed by EDX and are given in Table 6. From Table 6, the percentage atomic content of iron (Fe) is decreased from 87.05 (polished mild steel) to 30.93 (inhibited mild steel). From Figure 7(c), the EDX spectra of inhibited samples show that the Fe peaks are remarkably suppressed, when compared with the EDX spectra of polished (Figure 7(a)) and corroded (Figure 7(b)) mild steel samples. The above suppression of Fe peaks is due to the formation of protective film on the surface of mild steel. This study is further supportive evidence of formation of protective layer on the surface of mild steel.

4. Conclusion

From the studies, the following points are concluded:(i)8-QSC is found to be a good anticorrosion organic molecule of mild steel in 1 M HCl solution.(ii)Anticorrosive activity was increased with increase in inhibitor concentration.(iii)EIS study proved that the studied inhibitor follows adsorption mechanism and controls the corrosion of mild steel in 1 M HCl solution.(iv)Polarization studies reveal that 8-QSC acts as a predominantly cathodic inhibitor.(v)The adsorption of studied inhibitor on the mild steel surface obeys Langmuir adsorption isotherm.(vi)The values of in all methods indicate that the inhibitor inhibits the corrosion of mild steel by strong physisorption.(vii)Inhibition efficiency obtained from weight loss measurements was in good agreement with EIS, Tafel, and LPR methods.(viii)SEM and EDX studies confirmed the formation of inhibitor film on the surface of mild steel.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

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Copyright © 2016 R. Ganapathi Sundaram and M. Sundaravadivelu. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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