Green Approaches to Corrosion MitigationView this Special Issue
Research Article | Open Access
Ramses Garcia Inzunza, Benjamín Valdez Salas, Rita Kharshan, Alla Furman, Michael Schorr Wienner, "Interesting Behavior of Pachycormus discolor Leaves Ethanol Extract as a Corrosion Inhibitor of Carbon Steel in 1 M HCl: A Preliminary Study", International Journal of Corrosion, vol. 2012, Article ID 980654, 8 pages, 2012. https://doi.org/10.1155/2012/980654
Interesting Behavior of Pachycormus discolor Leaves Ethanol Extract as a Corrosion Inhibitor of Carbon Steel in 1 M HCl: A Preliminary Study
The purpose of this paper is to evaluate the inhibitive action of an ethanol extract from the leaves of Pachycormus discolor (EEPD) on the corrosion of carbon steel in 1 M HCl at different temperatures; gravimetric method and electrochemical tests were conducted. Potentiodynamic polarization was used at room temperature and resistance polarization at different temperatures. Thermodynamic adsorption parameters are shown in order to demonstrate the spontaneous adsorption. The inhibition of EEPD was performed via adsorption of the extract species on the carbon steel surface. The ethanol extract obeys Langmuir adsorption isotherm. Potentiodynamic polarization results indicate that the ethanol extract acts as a mixed type inhibitor. The results revealed that the inhibition efficiency (IE) of EEPD increases (when the concentration is increased). Phytochemical and FTIR analyses are also presented in this work. It was found that the IE increases with the temperature in a 2.0% v/v solution which showed 94.52% IE at C and 97.89% at C.
Acid pickling is an accepted treatment of a metallic surface to remove impurities, stains, and steel rust with an acid solution, such as hydrochloric acid (HCl) and sulphuric acid (H2SO4), usually before subsequent processing such as extrusion, rolling, painting, galvanizing or plating with zinc, aluminum, and so forth. However, inhibitor application is required since the corrosive media impairs the metal used .
Another important treatment is the well acidizing that is achieved by pumping hydrochloric acid into the well which is useful to dissolve limestone, dolomite, and calcite cement between the sediment grains of the reservoir rocks. In order to protect the integrity of the already completed well, inhibitor additives are introduced to the well to prohibit the well steel casting corroding with the acid.
The purpose of the present work is to show an alternative corrosion inhibitor based on endemic plant of Baja California, Mexico that will control the corrosion problem and will not damage the environment due to its biodegradable properties.
2. Experimental Procedure
2.1. Preparation of Carbon Steel Specimen
Specimens of carbon steel 1018 (AISI) were mechanically cut into coupons of size 5 cm × 1.2 cm × 0.2 cm and were provided with a hole of a uniform diameter to facilitate the suspension of the coupons in the test solution for the application of the weight loss method. For electrochemical studies, cylindrical carbon steel 1018 were used as a working electrode, with a 1 cm² area exposed and the rest being covered. The chemical composition of this steel is 0.15–0.20% C, 0.60–0.90% Mn, 0.04 (max) P, 0.05 (max) S and the remainder is Fe. The working electrode was polished with sand papers from 100 to 600 grades and subsequently washed with methanol and then stored in a desiccator . Accurate weight of the samples was obtained using an electronic balance METTLER TOLEDO.
2.2. Preparation of the Plant Extract
The leaves of the Pachycormus discolor were taken, dried in a desiccator SECADOR, and then well grounded into powder. Then 70 gr of this dry plant material remains in maceration with n-hexane, three times, at a rate of 20 volumes of solvent per 1 gr mass of plant material, kept stirred at room temperature for at least 4 hours each time. Filtering was met on the three portions of the extract. The distillation of solvents leads to a waxy mass, which was discarded for the study of corrosion inhibition.
Immediately after, the same plant material was kept under stirring three times for 6 hours at room temperature (25°C) at a rate of 10 volume of Ethanol (80% v/v) per 1 gr of dry and shattered leaves in order to extract the active components. The three portions were mixed, and then most of the solvent was eliminated by azeotropic distillation of ethanol at reduced pressure, prolonging the necessary distillation and/or increasing depression as possible. Do not exceed 45°C.
Concentrated solutions of corrosion inhibitor were prepared from the ethanol extract and were added to 1 M HCl at the range of 0.005% to 2.0% (v/v).
2.3. Infrared Analysis
IR analysis was carried out using a PERKIN-ELMER100 FTIR spectrometer to determine the functional groups of the ethanol extract.
2.4. Phytochemical Screening
Phytochemical screening was carried out on the ethanol extract of the leaves of Pachycormus discolor . The plant extract were screened for various compounds.
2.5. Weight Loss Method
The polished and preweighed carbon steel coupons of uniform size were tied with threads and suspended in 50 mL test solutions (in duplicate), with and without the inhibitor at 1% and 2% (v/v) concentrations for various time intervals. The coupons were washed, dried, and weighed. Then the weight loss was calculated.
The parameters used in this study are the following:(1)Time: 1.5 h, 4.5 h, 6.5 h, 21 h, 48 h, 109 h.(2)Inhibitor concentration: 1%, 2% (v/v).
The corrosion rate of the coupon of carbon steel 1018 was determined according to the loss in weight as a function of time. Where, and are the weight before and after the corrosion, respectively. is the total area of the coupon and t the corrosion time. From this data, inhibition efficiency (IE) was calculated.
The inhibition efficiency is given by the following: where, is the corrosion rate without inhibitor. is the corrosion rate with inhibitor.
2.6. Electrochemical Measurements
The electrochemical analysis was performed using a three electrode system . The carbon steel working electrode, saturated calomel (SCE) reference electrode, and high purity graphite counter electrodes were used in the corrosion cell. Measurements were performed using a Gamry Instrument Potentiostat/Galvanostat/ZRA PC 4/300 and DC 105 Corrosion Technique software.
The working electrode was polished with 120 to 600 grit sand paper, washed with methanol, and dried. Instead of a salt bridge, a Luggin capillary arrangement was used to keep SCE on the working electrode to avoid the ohmic contribution. The polarization plots were obtained 10 minutes after the working electrode was immersed in the solution using Tafel Technique at room temperature (23°C). Applying a scan rate of 1 mV/s in a range from −250 mV to +250 mV versus corrosion potential of the working electrode measured against SCE.
The inhibition efficiency was calculated using the formula  where is corrosion current without inhibitor. is corrosion current with inhibitor.
Values of linear polarization resistance were obtained using the polarization resistance technique at 23°C, 40°C, 60°C, and 75°C. The scan rate was 0.125 mV/s in a range from −0.20 to 0.20 mV versus corrosion potential of the working electrode measured against SCE.
The inhibition efficiency was calculated using the formula  where is the polarization resistance in the presence of inhibitor at each temperature. is the polarization resistance in the absence of inhibitor at each temperature.
3. Results and Discussion
3.1. Weight Loss Studies
The inhibitor was tested at two different concentrations 1% and 2% (v/v); their corresponding corrosion rates and inhibition efficiencies are presented in Tables 1 and 2, respectively. The corrosion rate decreases as the inhibitor concentration increases.
The corrosion rate diminishes 6 to 9 times after about 109 hours of immersion time, and the data are shown in Table 1.
The addition of inhibitors increases the IE, irrespective of the time of immersion. This may be due to the adsorption of phytochemical constituents of the extracts on the metal surface. The results related with the effect of time of different inhibitor concentrations for carbon steel 1018 immersed in 1 M HCl are also shown in Table 2. The inhibition efficiency is higher when the immersion time is increasing. The highest efficiency (93.50%) was obtained with the 2% v/v of inhibitor concentration after 109 hr testing.
3.2. Polarization Studies
The effect of the inhibitor concentration is shown in Figure 1 which presents the anodic and cathodic potentiodynamic polarization measurements of carbon steel 1018 in 1 M HCl solution at room temperature with EEPD. The electrochemical corrosion parameters: current density , cathodic and anodic Tafel slopes ( and ), and the percentage efficiency (IE) for the corrosion inhibition of carbon steel 1018 in 1 M HCl at room temperature at different concentrations of the plant extract are given in Table 3.
Polarization studies revealed that the corrosion current density decreased noticeably with the addition of the extract. Further, there was an anodic shift of the value from −471 mV (blank) to −432 mV at 2% v/v indicating that the Pachycormus discolor leaves extracts acted as an anodic inhibitor  for carbon steel 1018 in 1 M HCl, which was supported by the gradual and significant decrease of the anodic Tafel slope, is 113.9 mV/decade of blank to 71.0 mV/decade at 2% v/v. In lower inhibitor concentrations, the values of the cathodic Tafel slopes were decreasing too, though not markedly. This means that the extract must have acted by blocking anodic sites and also cathodic site to some extent, and the extract contained the active molecules which behaved as mixed type of inhibition.
3.3. Effect of Temperature
The effect of the temperature on the corrosion rate of carbon steel 1018 in the absence and in the presence of various inhibitors concentrations was studied at a temperature range from 23°C to 75°C, using the polarization resistance electrochemical measurement (Table 4). It was found that the polarization resistance in the absence and in the presence of inhibitor decreases with the increase in temperature, but the polarization resistance value is much greater for an inhibited acid solution than the uninhibited acid solution.
Regarding the 2% v/v inhibitor concentration, it shows an interesting behavior since the values of polarization resistance decrease with an increase in the temperature, though, it is not remarkable; actually the IE increased because the polarization resistance values are much higher for the uninhibited solution at 2% v/v than the uninhibited acid solution. The IE at 75°C is 97.89%.
The effect of temperature on the inhibited acid metal reaction is highly complex because many changes occur on the metal surface such as rapid etching and desorption of inhibitor and the inhibitor itself may undergo decomposition and/or rearrangement. However, it was found that the few inhibitors with acid metal systems have specific reactions which are as effective at high temperature as they are at low temperature [20–23].
3.4. Adsorption Isotherms
The primary step in the mechanism of action of the inhibitors in acid solutions is generally the adsorption on the metal surface, which is usually oxide free in acid solutions. Bockris states that  the adsorption of an organic substance onto the metal surface can be expressed in the following exchanger reaction: where is the number of water molecules displaced of the metal surface by one molecule of the adsorbed inhibitor; the value of depends on the transversal section of the organic molecule area with respect to the water molecule. The adsorption of the organic molecules occurs because the interaction between the energy on the metal surface and the inhibitor is greater than the interaction of the energy on the metal surface and the water molecules. When the equilibrium of the process described in (5) is reached, it is possible to obtain diverse expressions of the adsorption isotherm plots, and thus, the degree of surface coverage can be plotted as a function of the inhibitor concentration under test.
From Table 4, it can be concluded that increases with the inhibitor concentration; this is attributed to more adsorption of inhibitor molecules onto the carbon steel surface. The surface coverage values for different concentrations of the inhibitor in an acid medium have been evaluated from the polarization resistance data. The data was plotted graphically to obtain a suitable adsorption isotherm (Figure 2).The Langmuir adsorption isotherm  was applied to analyze its mechanism by the following: where is the inhibitor concentration in mL L−1 in the electrolyte, and (mL−1 L) is the equilibrium constant for the adsorption/desorption process.
The adsorption parameters from Langmuir adsorption isotherms are estimated and given in Table 5. It indicates that the inhibitor obeys the Langmuir model since the experimental data presents adequate curve fittings for the applied adsorption isotherms; the correlation coefficients were in the range: and also the slopes tend to be close to a unit.
The value demonstrates that it is affected by the temperature; when the temperature increases from 23°C to 40°C, decreases as a result, on the other hand, when the temperature increased from 65 to 75, the value of increased as well; however, the value that is obtained at room temperature (23°C) is much greater than the values at other temperatures. This means that the strength of adsorption is higher.
3.5. Thermodynamic Adsorption Isotherms
Thermodynamic adsorption data, such as change in free energy , enthalpy of adsorption , and the entropy of adsorption , can be calculated depending on the estimated values of from adsorption isotherms  at different temperatures as follows.
The values at all studied temperatures can be calculated from the following : where is the concentration of water molecules (in mL L−1) at the metal/solution interface. Then, the obtained values are plotted versus (Figure 3) in accordance with the basic equation : A straight line of interception represents the values. By introducing the values in (8), the values are calculated at all studied temperatures. As it can be observed in Figure 3, a segmented straight line of three opposite slopes was obtained in 1 M HCl indicating the existence of three sets of adsorption sites with different energetic enthalpies of adsorption, leading to the occurrence of a comprehensive adsorption.
The most negative value of occurs at room temperature (23°C); furthermore, the negative value of indicates that the adsorption of the inhibitor’s molecules is an exothermic reaction.
In addition, decreases (becomes more negative) with an increasing temperature in the range from 60°C to 75°C; it also shows the positive value of , indicating the occurrence of an endothermic process at which increasing the temperature facilitates the adsorption of the molecules.
The negative values of (Table 6) are accompanied with the exothermic adsorption process, which agrees with the expected event; when the adsorption is an exothermic process, it must be accompanied by a decrease (becomes more negative) in the entropy change .
Moreover, the value of the adsorption heat ) gives valuable information about the mechanism of the inhibitor adsorption. According to the listed values of (Table 6) it can be explained by the following.Both endothermic ( kJ mol−1) and exothermic adsorption behaviors were determined depending on the exact range of the applied temperatures. The average of is about −22.15 kJ mol−1 which is larger than the common physical adsorption heat, but smaller than the common chemical adsorption heat ; it probably indicates that both physical and chemical adsorption took place.
3.6. Infrared Analysis
The IR spectra (Figure 4) of the extract of Pachycormus discolor contain bands which correspond to: phenolic hydroxyl groups (3379.39 cm−1); carbonyl groups (1715 cm−1), aromatic C=C bending (1613 cm−1), =C–H out of plane bending (878.79 and 750.78 cm−1), two bands appear for the C–O stretching vibrations in esters in 1324 and 1205 cm−1.
3.7. Phytochemical Screening
Phytochemical screening was carried out on the ethanol extract of the leaves of Pachycormus discolor. The plant extracts were screened for various compounds (Table 7).
Several papers that have been published show that compounds such as alkaloids may be responsible for the corrosion inhibitive effect in a hydrochloric acid medium [33, 34]. Other corrosion inhibitors [35, 36] contain lactones, saponins, polyphenols, and they are also effective.
In the present case, the mixture of the different compounds can be responsible for the corrosion inhibitive effect. There is no data about the main compound on the ethanol extract of the leaves of Pachycormus discolor.
4. Conclusions(i)The Ethanol extract of the leaves of Pachycormus discolor acts as a mixed type inhibitor for the corrosion of carbon steel 1018 in 1 M HCl. (ii)Weight loss studies, polarization studies, electrochemical and polarization resistance measurements are in good agreement. (iii)The effect of immersion time of EEPD showed maximum efficiency in 109 hours at room temperature at 2% v/v inhibitor concentration. (iv)The polarization resistance increases with the amount of the inhibitor. (v)The adsorption of Pachycormus discolor on the carbon steel 1018 surface in hydrochloric acid obeys the Langmuir adsorption isotherm model. (vi)The effect of temperature revealed that both physical and chemical adsorption take place. (vii) The negative value of free energy change of adsorption indicates that the adsorption of the inhibitor on carbon steel 1018 surface was spontaneous. (viii)The inhibition efficiency of EEPD at room temperature is greater than at higher temperatures, except at 2% v/v inhibitor concentration.
- H. H. Uhlig, “Corrosión y control de corrosión,” Urmo, 1979.
- B. T. Kilbourn, “Ressources en lanthanides et yttrium, production de composés de ces éléments, utilisations dans les céramiques de haute technologie,” Ceramic Engineering and Science Proceedings, vol. 6, no. 9-10, pp. 1331–1341, 1985.
- M. Bethencourt, F. J. Botana, J. J. Calvino, M. Marcos, and M. A. Rodríguez-Chacón, “Lanthanide compounds as environmentally-friendly corrosion inhibitors of aluminium alloys: a review,” Corrosion Science, vol. 40, no. 11, pp. 1803–1819, 1998.
- M. A. Arenas, A. Conde, and J. J. de Damborenea, “Cerium: a suitable green corrosion inhibitor for tinplate,” Corrosion Science, vol. 44, no. 3, pp. 511–520, 2002.
- S. M. El-Sawy, Y. M. Abu-Ayana, and F. A. Abdel-Mohdy, “Some chitin/chitosan derivatives for corrosion protection and waste water treatments,” Anti-Corrosion Methods and Materials, vol. 48, no. 4, pp. 227–234, 2001.
- E. Cano, P. Pinilla, J. L. Polo, and J. M. Bastidas, “Copper corrosion inhibition by fast green, fuchsin acid and basic compounds in citric acid solution,” Materials and Corrosion, vol. 54, no. 4, pp. 222–228, 2003.
- D. J. Choi, Y. W. Kim, and J. G. Kim, “Development of a blended corrosion, scale, and microorganism inhibitor for open recirculating cooling systems,” Materials and Corrosion, vol. 52, no. 9, pp. 697–704, 2001.
- G. Moretti, F. Guidi, and G. Grion, “Tryptamine as a green iron corrosion inhibitor in 0.5 M deaerated sulphuric acid,” Corrosion Science, vol. 46, no. 2, pp. 387–403, 2004.
- S. A. Abd El-Maksoud , “The effect of organic compounds on the electrochemical behaviour of steel in acidic media. A review,” International Journal of Electrochemical Science, vol. 3, pp. 528–555, 2005.
- P. B. Raja and M. G. Sethuraman, “Natural products as corrosion inhibitor for metals in corrosive media—a review,” Materials Letters, vol. 62, no. 1, pp. 113–116, 2008.
- C. Chandler, M. Kharshan, and A. Furman, “Sugar beets against corrosion,” Corrosion Reviews, vol. 20, no. 4-5, pp. 379–390, 2002.
- A. Y. El-Etre and Z. El-Tantawy, “Inhibition of metallic corrosion using ficus extract,” Portugaliae Electrochimica Acta, vol. 24, pp. 347–356, 2006.
- A. Lourenço, L. Cruz Lopez, and A. San Feliciano, “Extraccion, Fraccionamiento y Aislamiento de Compuestos Activos,” in Programa Iberoamericano de Ciencia y Tecnologia para el desarrollo (CYTED '10), Universidade Nova de Lisboa, Portugal. Universidade Metodista de Piracicaba, Brasil. Universidad de Salamanca, España, 2010.
- ASTM G5-94, “Standard Reference Test Method for Making Potentiostatic and Potentiodynamic Anodic Polarization Measurements,” 2004.
- M. Scendo, “Inhibition of copper corrosion in sodium nitrate solutions with nontoxic inhibitors,” Corrosion Science, vol. 50, no. 6, pp. 1584–1592, 2008.
- M. Bouklah and B. Hammouti, “Thermodynamic characterisation of steel corrosion for the corrosion inhibition of steel in sulphuric acid solutions by Artemisia,” Portugalie Electrochimica Acta, vol. 24, p. 461, 2006.
- ASTM G3-89, “Standard Practice for Conventions Applicable to Electrochemical Measurements in Corrosion Testing,” 2010.
- ASTM G31-72, “Standard Practice for Laboratory Immersion Corrosion Testing of Metals,” 2004.
- O. L. Riggs Jr., Corrosion Inhibitors, Edited by C. C. Nathan, NACE, Houston, Tex, USA, 1973.
- B. I. Ita and O. E. Offiong, “The study of the inhibitory properties of benzoin, benzil, benzoin-(4-phenylthiosemicarbazone) and benzil-(4-phenylthiosemicarbazone) on the corrosion of mild steel in hydrochloric acid,” Materials Chemistry and Physics, vol. 70, no. 3, pp. 330–335, 2001.
- S. N. Raicheva, E. Sokolova, and A. E. Stoyanova, “Some factor of the inhibitory effect of nitrogen-and sulphur-containing organic compounds on steel corrosion,” Bulgarian Chemical Communications, vol. 27, p. 363, 1994.
- M. M. Singh and A. Gupta, “Inhibition of mild steel corrosion in formic acid solution,” Bulletin of Electrochemistry, vol. 12, no. 9, pp. 511–516, 1996.
- M. H. Wahdan, A. A. Hermas, and M. S. Morad, “Corrosion inhibition of carbon-steels by propargyltriphenylphosphonium bromide in H2SO4 solution,” Materials Chemistry and Physics, vol. 76, no. 2, pp. 111–118, 2002.
- J. O. M. Bockris and D. A. J Swinkels,, “Adsorption of naphtalene on solid metal electrodes,” Journal of The Electrochemical Society, vol. 111, p. 735, 1964.
- I. Langmuir, “The constitution and fundamental properties of solids and liquids. II. Liquids,” Journal of the American Chemical Society, vol. 39, p. 1848, 1947.
- E. A. Noor , “Temperature effects on the corrosion inhibition of mild steel in acidic Solutions by aqueos extract of Fenugreek leaves,” International Journal of Electrochemical Science, vol. 2, pp. 996–1017, 2007.
- E. Khamis, “Effect of temperature on the acidic dissolution of steel in the presence of inhibitors,” Corrosion, vol. 46, no. 6, pp. 476–484, 1990.
- A. A. El-Awady, B. A. Abd-El-Nabey, and S. G. Aziz, “Kinetic-thermodynamic and adsorption isotherms analyses for the inhibition of the acid corrosion of steel by cyclic and open-chain amines,” Journal of the Electrochemical Society, vol. 139, no. 8, pp. 2149–2154, 1992.
- M. Elachouri, M. S. Hajji, M. Salem et al., “Some nonionic surfactants as inhibitors of the corrosion of iron in acid chloride solutions,” Corrosion, vol. 52, no. 2, pp. 103–108, 1996.
- B. V. Savithri and S. M. Mayanna, “Tetrabutyl ammonium iodide, cetyl pyridinium bromide and cetyl trimethyl ammonium bromide as corrosion inhibitors for mild steel in sulphuric acid,” Indian Journal of Chemical Technology, vol. 3, no. 5, pp. 256–258, 1996.
- J. M. Thomas and W. J. Thomas, Introduction to the Principles of Heterogeneous Catalysis, Academic Press, London, UK, 5th edition, 1981.
- G. Mu, X. Li, and G. Liu, “Synergistic inhibition between tween 60 and NaCl on the corrosion of cold rolled steel in 0.5 M sulfuric acid,” Corrosion Science, vol. 47, no. 8, pp. 1932–1952, 2005.
- P. B. Raja and M. G. Sethuraman, “Studies on the inhibitive effect of Datura stramonium extract on the acid corrosion of mild steel,” Surface Review and Letters, vol. 14, no. 6, pp. 1157–1164, 2007.
- M. Lebrini, F. Robert, and C. Roos, “Alkaloids extract from Palicourea guianensis plant as corrosion inhibitor for C38 steel in 1 M hydrochloric acid medium,” International Journal of Electrochemical Science, vol. 6, no. 3, pp. 847–859, 2011.
- M. Shyamala and P. K. Kasthuri, “The inhibitory action of the extracts of Adathodavasica, Eclipsa alba and Centellaasiatica on the Corrosion of Mild Steel in Hydrochloric acid medium –a comparative study,” International Journal of Corrosion, vol. 2012, Article ID 852827, 13 pages, 2012.
- I. E. Uwah, P. C. Okafor, and V. E. Ebiekpe, “Inhibitive action of ethanol extracts from Nauclea latifolia on the corrosion of mild steel in H2SO4 solutions and their adsorption characteristics,” Arabian Journal of Chemistry. In press.
Copyright © 2012 Ramses Garcia Inzunza 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.