Evaluation of Corrosion Inhibition of Mild Steel in 1 M Hydrochloric Acid Solution by <i>Mollugo cerviana</i>

Arockiasamy, P.; Sheela, X. Queen Rosary; Thenmozhi, G.; Franco, M.; Sahayaraj, J. Wilson; Santhi, R. Jaya

doi:https://doi.org/10.1155/2014/679192

International Journal of Corrosion

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Abstract Introduction Materials and Methods Results and Discussion Conclusion References Copyright Related Articles

Research Article | Open Access

Volume 2014 | Article ID 679192 | https://doi.org/10.1155/2014/679192

Evaluation of Corrosion Inhibition of Mild Steel in 1 M Hydrochloric Acid Solution by Mollugo cerviana

P. Arockiasamy,¹X. Queen Rosary Sheela,²G. Thenmozhi,¹M. Franco,³J. Wilson Sahayaraj,⁴and R. Jaya Santhi¹

Academic Editor: Sebastian Feliu

Received28 Jan 2014

Revised19 Jun 2014

Accepted08 Jul 2014

Published21 Jul 2014

Abstract

The inhibiting effect of methanolic extract of Mollugo cerviana plant on the corrosion of mild steel in 1 M HCl solution has been investigated by different techniques like potentiodynamic polarization, electrochemical impedance spectroscopy, and weight loss methods for five different concentrations of plant extract ranging from 25 to 1000 mg/L. The results indicated that the corrosion inhibition efficiency increased on increasing plant extract concentration till 500 mg/L and decreased on further increasing concentration. The extract was a mixed type inhibitor with the optimum inhibition concentration of 500 mg/L in potentiodynamic polarization. The adsorption of the plant extract on the mild steel surface was found to obey Langmuir adsorption isotherm. Surface analysis was also carried out to find out the surface morphology of the mild steel in the presence and in the absence of the inhibitor to find out its efficiency. The obtained results showed that the Mollugo cerviana extract acts as a good inhibitor for the corrosion of mild steel in 1 M HCl solution.

1. Introduction

Corrosion inhibitors have been widely studied in many industries to reduce the corrosion rate of metal surfaces in contact with aggressive medium [1–3]. Acidic solutions are commonly used in various industries and applications include acid pickling, industrial cleaning, acid rescaling, oil-well acidification, and petrochemical processes [4]. Among the acid solutions, hydrochloric acid is one of the most widely used in the pickling processes of metals.

Use of inhibitors is one of the most practical methods for protection against corrosion especially in acid solutions to prevent metal dissolution and acid consumption [5]. Mild steel in acid solution is widely used in various industrial processes and corrosion of mild steel known to occur in this environment. One of the effective methods to prevent corrosion is the use of organic inhibitors [6]. A great number of scientific studies have been devoted to the subject of corrosion inhibitors for mild steel in acidic media [2, 7–14].

Plant extracts are viewed as environmentally friendly and ecologically acceptable inhibitors. Plant products are low-cost, readily available, and renewable sources of materials. The extracts from their leaves, barks, seeds, fruits, and roots comprise of mixtures of organic compounds containing nitrogen, sulphur, and oxygen atoms and some [15–20] have been reported to function as effective inhibitors of metal corrosion in different aggressive environments. Generally, the inhibitive effect of plant extract is attributed to the adsorption of organic substances on the metal surface, blocking active sites or even forming a protective barrier.

In recent years, natural compounds such as herbal plants are employed as inhibitors in order to develop new cleaning chemicals for green environment. Several studies have been reported in the use of natural products as corrosion inhibitors in different media [21–30].

M. cerviana (L.) Ser. (Molluginaceae) has been widely used as a pot herb, enhances eyesight, reduces body odour, acts as a good antiseptic, and is used in the treatment of cough. The aerial plant of Mollugo cerviana was collected near Sathankulam, Tuticorin district, Tamil Nadu, India, in July 2010. The plant was identified and authenticated by Dr. V. Chelladurai, Research Officer (Rted), Botanist, and the specimen was deposited at Department of Botany, Auxilium College, Vellore.

The objective of this study is to evaluate the inhibitive effect of methanolic extract of M. cerviana as a green corrosion inhibitor on the mild steel in 1 M HCl solution. The corrosion performance was studied using different techniques like potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), and weight loss methods. The scanning electron microcopy (SEM) was used for its morphological studies.

2. Materials and Methods

2.1. Preparation of the Plant Extract

The fresh aerial parts of M. cerviana (500 g) were washed with water, air dried, powdered, and extracted with methanol (Merck) for 24 hrs. The methanolic solution was filtered and refluxed further to get a concentrated solution. The clear dark brown methanolic concentrated solution was dried under vacuum to get a semisolid liquid and it was stored in air tight container and preserved in the refrigerator for the further studies.

2.2. Preparation of Specimen

Mild steel specimens having nominal composition of 0.023% P; 0.04% Si; 0.017% Ni; 0.37% Mn; 0.078% C; 0.02% S; 0.002% Mo; Fe balance were used. Specimens of dimension 3 × 3 × 0.1 cm and 1 × 1 × 0.1 cm were used for weight loss and electrochemical studies. The specimens were embedded in epoxy resin leaving a working area of 1 cm². The surface preparation of the mechanically abraded specimens was carried out using different grades of silicon carbide emery paper (up to 1200 grit) and subsequent cleaning with acetone and rinsing with double-distilled water were done before each experiment.

2.3. Electrolyte

The electrolyte of 1 M HCl solution was prepared by diluting 37% HCl (Merck) using double-distilled water which is used as a corrosive solution. The five concentrations of M. cerviana extract varied from 25 to 1000 mg/L.

2.4. Electrochemical Measurements

Electrochemical measurements, including potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS), were performed in a conventional three electrode cell using a computer-controlled potentiostat/galvanostat (Autolab PGSTAT 302N potentiostat from Eco-Chemie, Netherlands). Platinum electrode was used as the counter electrode, Ag/AgCl, and 3 M KCl as the reference electrode, and the mild steel specimen was used as a working electrode (WE). The area of the WE exposed to the solution was approximately 1 cm².

Before each potentiodynamic polarization (Tafel) and electrochemical impedance spectroscopy (EIS) studies, the electrode was allowed to corrode freely and its open circuit potential (OCP) was recorded as a function of time up to 20 min, which was sufficient to attain a stable state. After this, a steady-state of OCP corresponding to the corrosion potential () of the working electrode was obtained. The potentiodynamic measurements were started from cathodic to the anodic direction () at a scan rate of 10 mVs⁻¹. Electrochemical impedance spectroscopy measurements were carried out using AC signals at the amplitude of 10 mV and measurement frequency from 100 kHz–10 mHz at the stable OCP. Fresh solution and fresh mild steel samples were used after each sweep.

2.5. Weight Loss Method

Triplicate steel specimens were immersed in 100 mL of electrolyte with and without the M. cerviana extract for 1, 24, and 72 hrs at room temperature. The cleaned specimens were weighed before and after immersion into the corrosive solution. The specimens were removed, rinsed with water and acetone, and dried. The loss of weight of the steel samples was determined using an analytical balance with the precision of mg. The weight loss measurements were performed according to ASTM standard G 31-72. The percentage inhibition efficiency (IE) was obtained from the following equation: where and are the weight of the mild steel in the absence and in the presence of inhibitor.

2.6. Surface Analysis

The surface morphology of mild steel specimens immersed in 1 M HCl in the absence and presence of 500 mg/L of M. cerviana extract at room temperature for 2 hrs was studied using Leica S440i, a scanning electron microscope (SEM) operated at a voltage of 20 kV with probe current 100 pA.

3. Results and Discussion

3.1. Potentiodynamic Polarization

The potentiodynamic anodic and cathodic polarization plots for mild steel specimens in 1 M HCl solution with and without the plant extract M. cerviana at five different concentrations are given in Figure 1. The respective electrochemical parameters including the values of corrosion current density (), corrosion potential (), cathodic Tafel slope (), anodic Tafel slope (), inhibition efficiency (IE), and surface coverage (θ) are given in Table 1. As the inhibitor concentration increased, the corrosion current densities of mild steel decreased till 500 mg/L of plant extract [25, 26]. This behavior is due to the adsorption of the inhibitor present in the plant extract on mild steel/solution interfaces. In this study, the maximum corrosion potential of mild steel was shifted to 20 mV cathodically with respect to the blank. From the potentiodynamic polarization curves (Figure 1), it is evident that both the anodic and the cathodic reactions are inhibited. So, the M. cerviana extracts act as a mixed type inhibitor with predominant cathodic effect.

The polarization resistance increased noticeably with the increase in M. cerviana concentration and the percentage of IE values also increased with inhibitor concentrations. The percentage of inhibition efficiency (%IE) was calculated from potentiodynamic polarisation curves based on the following equation: where is the corrosion current density in the absence of the inhibitor and is the corrosion current density in the presence of the inhibitor obtained from Tafel plots. The chosen plant extract showed the maximum IE of 89% at 500 mg/L. The high inhibition efficiency was due to the bonding of the adsorbed film of the inhibitor on the steel surface [31]. There is no significant change in corrosion potential with the addition of the extracts at different concentrations. The surface coverage is approximately 0.84 which is good to act as a corrosive inhibitor.

3.2. Electrochemical Impedance Spectroscopy

The Nyquist plots of mild steel in 1 M HCl solution in the absence and in the presence of M. cerviana extract at different concentration as inhibitor during an immersion time of 20 min at room temperature are given in Figure 2. The depression in the figure is the characteristic of the inhomogeneities of the metal surface during corrosion [32]. The diameter of the capacitive loop stands for the resistance of the corrosion and it can be seen that the resistance decreases significantly with the decrease in diameter. Considering the impedance diagrams, the size of the capacitive loop increased by increasing the concentration of inhibitor. The Nyquist impedance plots were analyzed by fitting the experimental data to a simple equivalent circuit model given in Figure 3.

In this equivalent circuit (Figure 3), is the solution resistance, is the charge transfer resistance, and CPE is a constant phase element, which is placed in parallel to charge transfer resistance element. Thus, in these situations, pure double layer capacitors are better described by a transfer function with constant phase elements (CPE) to give a more accurate fit [33] and its impedance is given by where is proportionality coefficient, is the angular frequency, is the imaginary number, and is an exponent related to the phase shift and can be used as a measure of surface irregularity.

For ideal electrodes, when , CPE can be considered as a real capacitor. The charge transfer resistance () values are calculated based on the difference in impedance at lower and higher frequencies. According to the Helmholtz, the decrease in CPE can be attributed to increase in the thickness of the electrical double layer [34]. In EIS studies, the inhibition efficiency was calculated using (4) where and are charge transfer resistance in presence and absence of inhibitor obtained from the electrochemical impedance diagrams. The quantitative results of impedance measurements are given in Table 2. From the table result, it is clear that by increasing the inhibitor concentration, the CPE values tend to decrease and the values increase. Polarization resistance increases from 50.1 to 839.7 Ω cm² and double layer capacitance decreases from 0.092 to 0.046 μF/cm² with the increase of M. cerviana extract concentration. The solution resistance is approximately constant. The decrease in this capacitor values can be attributed to the formation of a protective layer on the electrode surface [35]. The increase in the polarization resistance leads to an increase in inhibition efficiency. The results also indicate that the increase of charge transfer resistance is related to a decrease in the double layer capacitance up to 500 mg/L. The effect is reversed with further increase in the concentration of the extract as seen in the result. As the concentration of the plant extract increased above 500 mg/L, the corrosion resistance decreased. In fact, the highest inhibition efficiency was reached at 500 mg/L of the plant extract which is considered to be an optimum inhibitor concentration. The surface coverage is approximately 0.95 which is found to be good to act as an anticorrosive agent. The results obtained from EIS method is in good agreement with the linear polarization and weight loss measurements.

3.3. Weight Loss Method

Weight loss data of mild steel in 1 M HCl in the absence and in the presence of various concentrations of inhibitor were obtained. This physical measurement is a direct answer to find out corrosive environments and the average corrosion rate. The variation of inhibition efficiency at different immersion times like 1, 24, and 72 hrs at room temperature in 1 M HCl is shown in Table 3. It has been observed that 500 mg/L of M. cerviana extract is considered to be an optimum concentration that exhibits higher efficiency against corrosion of mild steel. The results from the Table 3 also show that the corrosion rate decreases with increase in the concentration of the inhibitor in HCl and the maximum surface coverage is found to be 0.926 at 500 mg/L. There is considerable decrease in inhibition efficiency above 500 mg/L. The inefficiency above 500 mg/L may be due to weakening of metal-inhibitor interactions, resulting in the replacement of inhibitor by water or chlorine ions with decrease in inhibition efficiency [36]. The increasing inhibition efficiency and decreasing corrosion rate were attributed to the adsorption of inhibitor on the metal surface. From this result, it is clear that the extract is adsorbed at the corrosion sites of mild steel surface responsible for anticorrosion activity. The mild steel gets blocked and the adsorbed film of inhibitor acts as a physical barrier between mild steel and corrosion medium.

The inhibition increased with an increase in the immersion time and stabilized after 72 hrs with the inhibition rate of 92.6%. The results obtained from the weight loss measurement are in good agreement with those obtained from the other electrochemical methods.

3.4. Adsorption Isotherm

The interaction between an inhibitor and the mild steel surface can be described by the adsorption isotherm. To obtain the adsorption isotherm, the degree of surface coverage is calculated from the equation . It was determined at different inhibitor concentration using Langmuir adsorption isotherm and it can be expressed as where is equilibrium constant of adsorption and is the inhibition concentration. Many researchers have explained the Langmuir adsorption isotherm with an interaction of adsorbed species on the metallic surfaces [37, 38]. The Langmuir adsorption isotherm was drawn by plotting versus , considering the values from weight loss method at 72 hrs, potentiodynamic polarization, and EIS measurements at room temperature for mild steel in 1 M HCl at different concentration of inhibitors, and the graph is shown in Figure 4. The straight line obtained in the graph clearly shows that the chosen inhibitor obeys the Langmuir adsorption isotherm. From this, it can be concluded that the M. cerviana extract can act as a good inhibitor against corrosive materials.

3.5. Surface Analysis

The surface analysis was carried out using SEM for the mild steel surface immersed in 1 M HCl solution in the absence and in the presence of 500 mg/L of inhibitor. The SEM images of the mild steel, 1 M HCl, and with the inhibitor are given in Figure 5. A significant surface damage was observed on the mild steel, which was immersed in 1 M HCl solution (Figure 5(b)) indicating that the surface is highly corroded. The surface of the corroded area of the mild steel (5B) was protected with the addition of the inhibitor as is evident from the surface morphology (Figure 5(c)) and the presence of the inhibitor at the optimum concentration exhibited a smooth surface indicating restricted corrosion unlike 5B. The SEM images clearly indicate that the mild steel surface was protected from corrosion in the presence of plant extract which is acting as a corrosion inhibitor. In other words, the M. cerviana extract inhibits corrosion of mild steel in 1 M HCl solution. These results are in good agreement with the other methods like electrochemical and weight loss measurements.

(a)

(b)

(c)

4. Conclusion

M. cerviana extracts acted as an effective corrosion inhibitor for mild steel in 1 M HCl solution. The polarization studies showed that M. cerviana extract was a mixed type inhibitor and its corrosion efficiency increased with the inhibitor concentration. From the EIS plots of mild steel, it is clear that the charge transfer resistance increased with increase in M. cerviana extract. Inhibition efficiency obtained from weight loss measurements was in good agreement with polarization and EIS methods. The adsorption of the M. cerviana extracts of mild steel in 1 M HCl solution obeys the Langmuir adsorption isotherm and the SEM studies showed the formation of inhibitor film on mild steel surface.

Conflict of Interests

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

Acknowledgment

The authors are grateful to Mrs. Anju M Pillai, Thermal Systems Group, ISRO Satellite Centre, Bangalore 560 017, India, for her invaluable guidance and support.

References

M. Christov and A. Popova, “Adsorption characteristics of corrosion inhibitors from corrosion rate measurements,” Corrosion Science, vol. 46, no. 7, pp. 1613–1620, 2004.
View at: Publisher Site | Google Scholar
P. C. Okafor, X. Liu, and Y. G. Zheng, “Corrosion inhibition of mild steel by ethylamino imidazoline derivative in CO₂-saturated solution,” Corrosion Science, vol. 51, no. 4, pp. 761–768, 2009.
View at: Publisher Site | Google Scholar
L. Herrag, B. Hammouti, S. Elkadiri et al., “Adsorption properties and inhibition of mild steel corrosion in hydrochloric solution by some newly synthesized diamine derivatives: experimental and theoretical investigations,” Corrosion Science, vol. 52, no. 9, pp. 3042–3051, 2010.
View at: Publisher Site | Google Scholar
S. Cheng, S. Chen, T. Liu, X. Chang, and Y. Yin, “Carboxymethylchitosan + Cu²⁺ mixture as an inhibitor used for mild steel in 1 M HCl,” Electrochimica Acta, vol. 52, no. 19, pp. 5932–5938, 2007.
View at: Publisher Site | Google Scholar
L. R. Chauhan and G. Gunasekaran, “Corrosion inhibition of mild steel by plant extract in dilute HCl medium,” Corrosion Science, vol. 49, no. 3, pp. 1143–1161, 2007.
View at: Publisher Site | Google Scholar
E. Bayol, T. Gürten, A. A. Gürten, and M. Erbil, “Interactions of some Schiff base compounds with mild steel surface in hydrochloric acid solution,” Materials Chemistry and Physics, vol. 112, no. 2, pp. 624–630, 2008.
View at: Publisher Site | Google Scholar
P. C. Okafor and Y. Zheng, “Synergistic inhibition behaviour of methylbenzyl quaternary imidazoline derivative and iodide ions on mild steel in H₂SO₄ solutions,” Corrosion Science, vol. 51, no. 4, pp. 850–859, 2009.
View at: Publisher Site | Google Scholar
Z. Zhang, S. Chen, Y. Li, S. Li, and L. Wang, “A study of the inhibition of iron corrosion by imidazole and its derivatives self-assembled films,” Corrosion Science, vol. 51, no. 2, pp. 291–300, 2009.
View at: Publisher Site | Google Scholar
M. Mahdavian and M. M. Attar, “Electrochemical behaviour of some transition metal acetylacetonate complexes as corrosion inhibitors for mild steel,” Corrosion Science, vol. 51, no. 2, pp. 409–414, 2009.
View at: Publisher Site | Google Scholar
X. Liu, P. C. Okafor, and Y. G. Zheng, “The inhibition of CO₂ corrosion of N80 mild steel in single liquid phase and liquid/particle two-phase flow by aminoethyl imidazoline derivatives,” Corrosion Science, vol. 51, no. 4, pp. 744–751, 2009.
View at: Publisher Site | Google Scholar
T. Arslan, F. Kandemirli, E. E. Ebenso, I. Love, and H. Alemu, “Quantum chemical studies on the corrosion inhibition of some sulphonamides on mild steel in acidic medium,” Corrosion Science, vol. 51, no. 1, pp. 35–47, 2009.
View at: Publisher Site | Google Scholar
F. G. Liu, M. Du, J. Zhang, and M. Qiu, “Electrochemical behavior of Q235 steel in saltwater saturated with carbon dioxide based on new imidazoline derivative inhibitor,” Corrosion Science, vol. 51, no. 1, pp. 102–109, 2009.
View at: Publisher Site | Google Scholar
J. M. Roque, T. Pandiyan, J. Cruz, and E. García-Ochoa, “DFT and electrochemical studies of tris(benzimidazole-2-ylmethyl)amine as an efficient corrosion inhibitor for carbon steel surface,” Corrosion Science, vol. 50, no. 3, pp. 614–624, 2008.
View at: Publisher Site | Google Scholar
Z. Ait Chikh, D. Chebabe, A. Dermaj et al., “Electrochemical and analytical study of corrosion inhibition on carbon steel in HCl medium by 1,12-bis(1,2,4-triazolyl)dodecane,” Corrosion Science, vol. 47, no. 2, pp. 447–459, 2005.
View at: Publisher Site | Google Scholar
A. Rauscher, G. Kutsan, and Z. Lukacs, “Studies on the mechanisms of corrosion inhibition by acetylenic compounds in hydrochloric acid solution,” Corrosion Science, vol. 35, no. 5–8, pp. 1425–1430, 1993.
View at: Publisher Site | Google Scholar
Z. Ahmad, Principles of Corrosion Engineering and Corrosion Control, Butterworth-Heinemann, London, UK, 2006.
H. Ashassi-Sorkhabi and E. Asghari, “Effect of hydrodynamic conditions on the inhibition performance of l-methionine as a “green” inhibitor,” Electrochimica Acta, vol. 54, no. 2, pp. 162–167, 2008.
View at: Publisher Site | Google Scholar
E. E. Oguzie, “Studies on the inhibitive effect of Occimum viridis extract on the acid corrosion of mild steel,” Journal of Materials chemistry and physics, vol. 99, no. 2-3, pp. 441–446, 2006.
View at: Publisher Site | Google Scholar
P. C. Okafor, M. E. Ikpi, I. E. Uwah, E. E. Ebenso, U. J. Ekpe, and S. A. Umoren, “Inhibitory action of Phyllanthus amarus extracts on the corrosion of mild steel in acidic media,” Corrosion Science, vol. 50, no. 8, pp. 2310–2317, 2008.
View at: Publisher Site | Google Scholar
I. Radojčić, K. Berković, S. Kovač, and J. Vorkapić-Furač, “Natural honey and black radish juice as tin corrosion inhibitors,” Corrosion Science, vol. 50, no. 5, pp. 1498–1504, 2008.
View at: Publisher Site | Google Scholar
K. M. Ismail, “Evaluation of cysteine as environmentally friendly corrosion inhibitor for copper in neutral and acidic chloride solutions,” Electrochimica Acta, vol. 52, no. 28, pp. 7811–7819, 2007.
View at: Publisher Site | Google Scholar
K. Srivastava and P. Srivastava, “Studies on plant materials as corrosion inhibitors,” British Corrosion Journal, vol. 16, no. 4, pp. 221–223, 1981.
View at: Publisher Site | Google Scholar
A. M. Abdel-Gaber, E. Khamis, H. Abo-ElDahab, and S. Adeel, “Inhibition of aluminium corrosion in alkaline solutions using natural compound,” Journal of Materials Chemistry and Physics, vol. 109, no. 2-3, pp. 297–305, 2008.
View at: Publisher Site | Google Scholar
A. M. Abdel-Gaber, “Effect of immersion time and temperature on the inhibition of the acid corrosion of zinc by fenugreek seeds extract,” International Journal of Applied Chemistry, vol. 3, p. 161, 2007.
View at: Google Scholar
I. H. Farooqi, M. A. Quraishi, and P. A. Saini, “Natural compounds as cooling water inhibitors for cooling systems,” in Proceedings of the EUROCORR'97, vol. 2, p. 347, 1997.
View at: Google Scholar
M. A. Quraishi, “Investigation of some green compounds as corrosion and scale inhibitors for cooling systems,” Corrosion, vol. 55, no. 5, pp. 493–497, 1999.
View at: Publisher Site | Google Scholar
Y. Li, P. Zhao, Q. Liang, and B. Hou, “Berberine as a natural source inhibitor for mild steel in 1 M H₂SO₄,” Applied Surface Science, vol. 252, no. 5, pp. 1245–1253, 2005.
View at: Publisher Site | Google Scholar
P. Sakthivel, P. V. Nirmala, S. Umamaheswari et al., “Corrosion inhibition of mild steel by extracts of Pongamia Glabra and Annona Squamosa in acidic media,” Bulletin of Electrochemistry, vol. 15, no. 2, pp. 83–86, 1999.
View at: Google Scholar
R. Kanojia and G. Singh, “An interesting and efficient organic corrosion inhibitor for mild steel in acidic medium,” Surface Engineering, vol. 21, no. 3, pp. 180–186, 2005.
View at: Publisher Site | Google Scholar
H. Al-Sehaibani, “Evaluation of extracts of Henna leaves as environmentally friendly corrosion inhibitors for metals,” Materialwissenschaft und Werkstofftechnik, vol. 31, no. 12, pp. 1060–1063, 2000.
View at: Publisher Site | Google Scholar
E. Khamis and N. M. Al Andis, “Herbs as new type of green inhibitors for acidic corrosion of steel,” Materialwiss Werkst, vol. 33, no. 9, pp. 550–554, 2002.
View at: Google Scholar
V. R. Saliyan and A. V. Adhikari, “Quinolin-5-ylmethylene-3-{[8-(trifluoromethyl)quinolin-4-yl]thio}propanohydrazide as an effective inhibitor of mild steel corrosion in HCl solution,” Corrosion Science, vol. 50, no. 1, pp. 55–61, 2008.
View at: Publisher Site | Google Scholar
I. D. Raistrick, D. R. Franceschetti, and J. R. Macdonald, Impedance Spectroscopy, Theory, Experimental, and Applications, John Wiley & Sons, Hoboken, NJ, USA, 2nd edition, 2005, E. Barsoukov, J. R. Macdonald, Eds.
Y. Tang, X. Yang, W. Yang, R. Wan, Y. Chen, and X. Yin, “A preliminary investigation of corrosion inhibition of mild steel in 0.5 M H2SO4 by 2-amino-5-(n-pyridyl)-1,3,4-thiadiazole: polarization, EIS and molecular dynamics simulations,” Corrosion Science, vol. 52, no. 5, pp. 1801–1808, 2010.
View at: Publisher Site | Google Scholar
M. Lebrini, M. Lagrenée, H. Vezin, M. Traisnel, and F. Bentiss, “Experimental and theoretical study for corrosion inhibition of mild steel in normal hydrochloric acid solution by some new macrocyclic polyether compounds,” Corrosion Science, vol. 49, no. 5, pp. 2254–2269, 2007.
View at: Publisher Site | Google Scholar
G. Gunasekaran and L. R. Chauhan, “Eco friendly inhibitor for corrosion inhibition of mild steel in phosphoric acid medium,” Electrochimica Acta, vol. 49, no. 25, pp. 4387–4395, 2004.
View at: Publisher Site | Google Scholar
E. Bayol, K. Kayakirilmaz, and M. Erbil, “The inhibitive effect of hexamethylenetetramine on the acid corrosion of steel,” Materials Chemistry and Physics, vol. 104, no. 1, pp. 74–82, 2007.
View at: Publisher Site | Google Scholar
L. Tang, G. Mu, and G. Liu, “The effect of neutral red on the corrosion inhibition of cold rolled steel in 1.0 M hydrochloric acid,” Corrosion Science, vol. 45, no. 10, pp. 2251–2262, 2003.
View at: Publisher Site | Google Scholar

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Copyright © 2014 P. Arockiasamy et al. 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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