Sucrose fatty esters from underutilized seed oil of Terminalia catappa as potential steel corrosion inhibitor in acidic medium doi:10.5599/jese.316 287 J. Electrochem. Sci. Eng. 6(4) (2016) 287-294; doi: 10.5599/jese.316 Open Access : : ISSN 1847-9286 www.jESE-online.org Original scientific paper Sucrose fatty esters from underutilized seed oil of Terminalia catappa as potential steel corrosion inhibitor in acidic medium Adewale Adewuyi, Omolade Rahman Bello*, Rotimi A. Oderinde* Department of Chemical Sciences, Faculty of Natural Sciences, Redeemer’s University, Ede, Osun state, Nigeria *Industrial Unit, Department of Chemistry, University of Ibadan, Ibadan, Oyo state, Nigeria Corresponding author: walexy62@yahoo.com; Phone: +2348035826679 Received: June 7, 2016; Revised: November 17, 2016; Accepted: November 18, 2016 Abstract Corrosion of metals is a common problem which requires definite attention. In response to this, the oil was extracted from the seed of Terminalia catappa and used to synthesize sucrose fatty esters via simple reaction mechanism which was considered eco-friendly and sustainable. The corrosion inhibition capacity of sucrose fatty esters for mild steel in 1 M HCl was studied using the weight loss method. It was shown that sucrose fatty ester inhibited corrosion process of mild steel and obeyed Langmuir isotherm. Corrosion rate and inhibition efficiency of sucrose fatty esters were found to reduce with increase of immersion time. The study presented sucrose fatty ester as a promising inhibitor of mild steel corrosion in acidic medium. Keywords Adsorption; Corrosion; Adsorption isotherm; Mild steel; Fatty esters Introduction Corrosion is usually taken as breaking down or wearing of materials, mostly metals, through chemical reactions. The most known form of corrosion is rusting, which takes place when iron combines with oxygen and water. Mild steels are known to contain carbon alloyed mainly with copper, chromium, phosphorus, nickel, etc. [1]. Generally, the mild steel shows some resistance to atmospheric corrosion which is attributed to its ability to develop a protective layer. It has already been shown that development of this layer depends on nature, amount and type of alloying elements in the steel and also on exposure, or corrosion initiator conditions [25]. Corrosion is the major problem encountered in the industries and areas involving surface equipment and processing facilities. This is seen mainly as leaks in tanks, casings, tubing, pipelines, and other equipment [6,7]. The problem of corrosion affects operations and equipment http://www.jese-online.org/ mailto:walexy62@yahoo.com J. Electrochem. Sci. Eng. 6(4) (2016) 286-294 Terminalia catappa AS STEEL CORROSION INHIBITOR 288 maintenance, which may lead to recurrent partial and even total process shutdown [8]. Use of highly concentrated acids for some industrial unit operations makes the environment corrosive to mild steel, carbon and low-alloy steels. Some of these acids include hydrochloric, hydrofluoric, acetic, or formic acids which are injected into the system during the acidizing stimulation process [9]. This has raised the need or search for a way to control or minimize corrosion. Although several efforts have been made in past, it is still almost impossible to fully prevent corrosion [10]. It is possible, however, to control the process in order to minimize the havoc it brings. Some control of corrosion has been achieved by use of several organic and organometallic compounds [11,12]. Even in very small amounts added to a corrosive environment, such compounds are expected to be effective and efficient in decreasing corrosion rates. In some cases, it has been noticed that these compounds are specific in their actions, being efficient only towards particular metals under specific environmental conditions. In other cases, aside being efficient, they were found toxic to the environment, human and animals [13,14]. Inhibition of corrosion is very important phenomenon. Without inhibition, corrosion rate can be extremely high and may go out of control, particularly at increasing temperatures. Due to this, it is important to develop inhibitors that will be effective, environmentally friendly, affordable and of industrial relevance, what would also be important for processes involving acid pickling, industrial cleaning, and acid descaling, where corrosion conditions are usually milder. Underutilized seed oils are resources which are readily available, cheap, environmentally friendly and affordable. They can be used as starting materials for production of useful products that can serve as corrosion inhibitors [15]. Terminalia catappa oil is an example of underutilized seed oil in Nigeria that can serve this purpose. Presently, the oil has no specific use and is usually being discarded as waste. Finding useful application for this oil will go a long way in making the environment cleaner. As has been reported by Matos et al. [16], the oil contains mainly palmitic (35.96 %), oleic (31.48 %) and linoleic (28.93 %) fatty acids. Presence of these fatty acids and level of unsaturation represent this oil useful for corrosion inhibitor production. The present work reports the synthesis of sucrose fatty ester from Terminalia catappa oil and examination of its ability to inhibit corrosion of mild steel in acidic condition. The effect of time and concentration of sucrose fatty acid ester on corrosion rate will also be examined. Experimental Materials The seeds of Terminalia catappa were collected from the Botanical garden, University of Ibadan, Oyo state, Nigeria. The seeds were air dried and subsequently ground in a laboratory mill. Dimethyl sulphoxide, hydrochloric acid and sucrose were purchased from Merck, Darmstadt, Germany. Further chemicals and all solvents used in this study were of analytical grade and were purchased from VWR International GmbH, Darmstadt. The dried seeds of Terminalia catappa were later extracted with n-hexane for 10 h using a soxhlet extractor [17]. Synthesis of sucrose fatty ester from Terminalia catappa oil For the synthesis of the sucrose fatty ester, 25 g of sucrose was transferred into a round bottom flask which previously contained dimethyl sulfoxide (55 mL). The mixture was heated and gently swirled to ensure complete dissolution of the sucrose in the solvent. Terminalia catappa oil (65 mL) was added to the resulting solution and followed by addition of K2CO3 (3 g). The flask with a stopper having thermometer inserted was placed on a heating mantle and allowed reaction to A. Adewuyi et al. J. Electrochem. Sci. Eng. 6(4) (2016) 287-294 doi:10.5599/jese.316 proceed for 9 h at an average temperature of 110 °C with occasional swirling. A thick brownish product was formed at the end of the reaction. At the end of reaction, the excess dimethyl sulfoxide was removed by distillation and the unreacted sucrose was removed by dissolving it in water. The residue of sucrose fatty ester was filtered, weighed and taken for FTIR analysis. Corrosion study In this study, the weight loss procedure was used for determination of corrosion rates. The mild steel sheets were obtained from the local market in Ibadan, Oyo state, Nigeria. The sheets were degreased in ethanol, dried in acetone, and stored before their use in corrosion studies. The sheets were cut into 4×3 cm size. The corrosion process was initiated by HCl, while the sucrose fatty ester was used as the inhibitor. The effect of both, initiator and inhibitor, on the corrosion rate was examined by varying the concentration of sucrose fatty ester (1 – 3 mg/L) and HCl (1 – 8 M). 1 M HCl solution was used as the control solution, while other solutions containing sucrose fatty ester were used as test solutions. Corrosion study was conducted under total immersion of mild steel sheets in 100 mL capacity beakers containing 50 mL test solution at room temperature (298 K). Mild steel sheets were weighed and separately suspended in different beakers containing solutions. The sheets were retrieved at 1 h interval progressively for 24 h, washed thoroughly in 20 % NaOH solution containing 200 g/L of zinc dust, rinsed severally in deionized water, cleaned, dried in acetone, and re-weighed. The weight loss (in grammes) was taken as difference in the weight of sheets before and after immersion in test solution [18]. The experiments were carried out in duplicate. Results and discussion Synthesis of sucrose fatty ester from Terminalia catappa oil The oil of Terminalia catappa has a light yellowish color and is liquid at room temperature. FTIR spectra of Terminalia catappa seed oil and that of the sucrose fatty ester showed some important absorption bands. For both, the oil and sucrose fatty ester, peaks were noticed at 1747 cm-1 and 1733.33 cm-1, respectively, what were attributed to C=O stretching of ester functional groups. Also, the bands at around 1164.62 cm-1 were ascribed to C─O vibrational frequencies in both oil and sucrose fatty ester. Signals that appeared at 2920.04 cm-1 in the oil and at 2931.42 cm-1 in the sucrose fatty esters, were taken to be due to C-H stretching of alkanes. Peaks at around 3011 cm-1 were considered to be due to C=C-H vibrational frequency of alkene. Broad and prominent peak at 3384.00 cm-1 was found only in the sucrose fatty ester and attributed to the O─H stretching; this peak suggested formation of the sucrose fatty ester. Corrosion study Weight loss during corrosion was calculated as difference in weights at an interval of 1 h. The relationship between weight loss of mild steel in 1 M HCl at different immersion times is presented in Figure 1. The weight loss of mild steel was found to increase with increase in time. It was observed that mild steel in the blank solution (solution without inhibitor) shows faster loss in weight than in the solution containing inhibitor. This observation indicates that presence of sucrose fatty esters in the solution is able to slow down the process of corrosion. J. Electrochem. Sci. Eng. 6(4) (2016) 286-294 Terminalia catappa AS STEEL CORROSION INHIBITOR 290 Figure 1. Relationship between weight loss of mild steel and immersion time in 1 M HCl The observed retardation of corrosion may be due to deposition or adsorption of sucrose fatty esters at the mild steel surface [18,19]. Figure 2 also revealed that the process of corrosion of mild steel increases as the strength of the acidic solution increases. This suggests that presence of positively charged hydrogen ions in solution plays a role in attacking the surface of the mild steel for corrosion. Similar observation has been previously reported by Adewuyi et al. [15]. Figure 2. Effect of HCl concentration on weight loss of mild steel in presence (inhibitor) and absence (blank) of sucrose fatty esters Corrosion rate was determined using the following expression: W R At   (1) In Eq. (1), R (g cm-2 h-1) is the corrosion rate, ∆W is the average weight loss after immersion, A is the surface area of mild steel and t is the total time (24 h) of immersion. Inhibition efficiency (Ew / %) for the process was determined as follows: t w 0 0 / % 100 R E R R         (2) In Eq. (2), Rt and R0 are corrosion rates of mild steel in solutions with and without inhibitor, respectively. The plots of corrosion rates against immersion time are presented in Figure 3 which revealed that with increase of immersion time, the rate of corrosion becomes reduced in both solutions, i.e. blank and solution with inhibitor. 0 0,02 0,04 0,06 0,08 0,1 0 1 2 3 4 5 6 7 8 9 Immersion time, h w e ig h t lo ss , g 0 0,01 0,02 0,03 0,04 0,05 0,06 0,07 0,08 0,09 0 2 4 6 8 10 Concentration of HCl, M W lo ss , g A. Adewuyi et al. J. Electrochem. Sci. Eng. 6(4) (2016) 287-294 doi:10.5599/jese.316 Figure 3. Corrosion rate versus immersion time for mild steel corrosion in presence and absence of sucrose fatty esters Corrosion is obviously slower in the sucrose fatty ester containing solution, what could be due to the covering of mild steel surface by this inhibitor. For the blank solution, however, this observation may be due to corrosion caused reduction of available surface area during time of immersion. Inhibition efficiency of sucrose fatty esters against mild steel corrosion was also found to reduce with time as shown in Figure 4. It has already been reported that inhibitive mechanism of most organic compounds is based on their adsorption at corroding metal surfaces [2023]. Therefore, desorption of inhibitor from the surface of mild steel as immersion time increases can possibly explain the results given in Figure 4. Figure 4. Relationship between inhibition efficiency and immersion time for mild steel corrosion Table 1. Comparison of the concentration of HCl, weight loss, rate and inhibition efficiency during the corrosion of mild steel Concentration of SFE, g/L Weight loss, g Concentration rate, (g/cm2)/h Inhibition efficiency, % 1.00 0.018 0.0015 34.80 2.00 0.022 0.0018 33.30 4.00 0.031 0.0026 27.80 6.00 0.048 0.0040 20.00 8.00 0.067 0.0056 15.10 Corrosion rate and weight loss were found to increase, while inhibition efficiency was found to decrease as the concentration of HCl increased. It could be inferred from the results in Table 1 that the corrosion initiator’s solution strength was influential in promoting corrosion. It seems that as 0 0,0005 0,001 0,0015 0,002 0,0025 0 1 2 3 4 5 6 7 8 9 Immersion time, h R a te , (g /c m 2 )/ h 0 5 10 15 20 25 30 35 40 0 2 4 6 8 10 Immersion time, h In h ib it o n e ff ic ie n cy , % J. Electrochem. Sci. Eng. 6(4) (2016) 286-294 Terminalia catappa AS STEEL CORROSION INHIBITOR 292 the strength of HCl increased, there were more species in solution to corrosively attack the metal surface, increasing thus corrosion rate. Reduction of inhibition efficiency may be due to the fact that as concentration of HCl increased, inhibitor molecules have more contending species at the metal surface and so they are less effective in adsorption/deposition. The effect of concentration of inhibitor on the corrosion rate, inhibitor efficiency and weight loss is presented in Table 2. Data in Table 2 show that inhibition efficiency increased, while corrosion rate is reduced with concentration of sucrose fatty ester. As has already been mentioned above, the observed reduction of corrosion rate may be due to the ability of inhibitor to cover or adsorb at the metal surface. Table 2. Comparison of the concentration of sucrose fatty ester, weight loss, corrosion rate and inhibition efficiency during corrosion of mild steel Concentration of SFE, g/L Weight loss, g Concentration rate, (g/cm2)/h Inhibition efficiency, % 1.00 0.0280 0.00183 20.43 1.50 0.0220 0.00173 24.78 2.00 0.0190 0.00166 27.83 2.50 0.0193 0.00161 30.00 3.00 0.0180 0.00150 34.78 SFE = Sucrose fatty esters Adsorption isotherm Interaction between the metal surface and inhibitor was subjected to adsorption isotherm. The surface coverage () was derived from the expression: t 0 0 R R R         (3) In Eq. (3), Rt and R0 are corrosion rates of mild steel with and without inhibitor, respectively. The correlation between  and amount of inhibitor in the corroding medium was determined by Langmuir adsorption isotherm which can be expressed as: ads 1C C K   (4) In Eq. (4), C is the inhibitor concentration, θ is the surface coverage and Kads is the equilibrium constant of the inhibitor adsorption process. This model operates on the assumption that adsorption takes place only at specific homogenous sites of metal surface and that adsorption forms a monolayer [22]. As shown in figure 5, the plot of C/ versus C gave straight lines (r2 = 0.968), suggesting thus the monolayer adsorption of sucrose fatty esters at the surface of the mild steel. Figure 5. Langmuir adsorption plot for mild steel in 1 M HCl containing sucrose fatty esters 0 0,5 1 1,5 2 2,5 3 3,5 0 0,5 1 1,5 2 2,5 3 3,5 (C /θ ) / (m g /L ) Concentration, mg/L A. Adewuyi et al. J. Electrochem. Sci. Eng. 6(4) (2016) 287-294 doi:10.5599/jese.316 The essential characteristic of Langmuir isotherm was calculated as follows: ads 1 1 K K C   (5) In Eq. (5), KR is the equilibrium parameter, Kads is the Langmuir constant and C is the inhibitor concentration. The parameter KR indicates the shape of the isotherm accordingly. It has been reported that when KR > 1, adsorption is unfavourable; when KR = 1, adsorption is linear; when KR = 0, adsorption is irreversible and when 0 < KR< 1, adsorption is favourable [2426]. Here, the calculated KR values were < 1, confirming that the adsorption process was favourable and reversible. This also supports the findings that inhibition efficiency is reduced with time which may have been due to the possibility of desorption taking place at the surface of the metal over a period of time. Conclusion Sucrose fatty ester was synthesized from the seed oil of Terminalia catappa and evaluated for corrosion inhibition capacity against mild steel in acidic medium using HCl. The synthesis of the sucrose fatty ester was achieved using simple reaction mechanism which was analyzed using FTIR. The sucrose fatty esters inhibited corrosion of mild steel in 1 M HCl with inhibition efficiency increasing as the concentration of sucrose fatty esters increased and decreasing with increase in time. Inhibition of corrosion is going via adsorption of sucrose fatty ester on the surface of the metal which obeyed Langmuir isotherm. The study presents sucrose fatty ester from Terminalia catappa as the potential corrosion inhibitor of mild steel. Acknowledgement: The authors are most grateful to the Department of Chemistry, University of Ibadan, Ibadan, Oyo state and the Department of Chemical Sciences, Redeemer’s University, Ede, Osun state for supplying chemicals, equipment and laboratory space for this work. References [1] T. Murata, Weathering steel, in: R.W. Revie (Ed.), Uhlig’s Corrosion Handbook, J. Wiley &Sons, New York, 2000, 569–580 [2] M. Morcillo, B. Chico, I. Díaz, H. Cano, D .de la Fuente, Corros. Sci. 77 (2013) 6–24. [3] Y. Oshida, E. B. Tuna, O. Aktören, K. Gençay, Int. J. Mol. Sci. 11 (2010) 1580-1678 [4] K. H. Lo, C. H. Shek, J. K. L. Lai, Mat. Sci. Eng. 65 (2009) 39-104 [5] H. Nady, Egypt. J. Petr. (2016) http://dx.doi.org/10.1016/j.ejpe.2016.02.004 [6] M. M. Oman, M. N. Shalaby, Mater. Chem. Phys.77 (2003) 261–269. [7] P. C. Okafor, X. Liu, Y. G. Zheng, Corros. Sci. 51 (2009) 761–768. [8] V. Garcia-Arriaga, J. Alvarez-Ramirez, M. Amaya, E. Sosa, Corros. Sci. 52 (2010) 2268–2279. [9] M. Finšgar, J. Jackson, Corros. Sci. 86 (2014)17–41 [10] D. Brondel, R. Edwards, A. Hayman, D. Hill, S. Mehta, T. Semerad, Oilfield Rev. 6 (1994) 4– 18. [11] M. Quraishi, D. Jamal, J. Am. Oil Chem. Soc.77 (2000) 1107–1111. [12] A. L. D. Q. Baddini, S. P. Cardoso, E. Hollauer, J. A. D. C. P. Gomes, Electrochim. Acta, 53 (2007) 434–446. [13] W. P. Singh, J. O. Bockris, Corrosion 96 (1996) 24-29 [14] D. I. Horsup, J. C. Clark, B. P. Binks, P. D. I. Fletcher, J. T. Hicks, Corrosion 66 (2010) 036001- 036014. [15] A. Adewuyi, A. Göpfert, T. Wolff, Ind. Crops Prod. 52 (2014) 439– 449 http://dx.doi.org/10.1016/j.ejpe.2016.02.004 J. Electrochem. Sci. Eng. 6(4) (2016) 286-294 Terminalia catappa AS STEEL CORROSION INHIBITOR 294 [16] L. Matos, J. M. Nzikou, A. Kimbonguila, C. B. Ndangui, N. P. G. Pambou-Tobi, A. A. Abena, Th. Silou, J. Scher, S. Desobry, Adv. J. Food Sci. Technol. 1 (2009) 72-77. [17] A. Adewuyi, A. Göpfert, T. Wolff, Central Eur. J. Chem. 11 (2013) 1368-1380. [18] A. Adewuyi, A. Göpfert, T. Wolff, Ind. Crops Prod. 52 (2014) 439– 449. [19] I. B. Obot, N. O. Obi-Egbedi, N. W. Odozi, Corros. Sci. 52 (2010) 923–926. [20] G. Y. Elewady, I. A. El-Said, A. S. Fouda, Int. J. Electrochem. Sci. 3 (2008) 177-190. [21] E. E. Ebenso, I. B. Obot, L. C. Murulana, Int. J. Electrochem. Sci. 5 (2010)1574 – 1586. [22] I. B. Obot, N. O. Obi-Egbedi, J. Current. Appl. Phy. 11 (2011) 382- 392. [23] A. Adewuyi, A. D. Adesina, R. A. Oderinde, Advances in Chemistry, 2014 (2014) 896965, http://dx.doi.org/10.1155/2014/896965. [24] Y. Ho, Polish J. Environ. Studies 15 (2006) 81-86. [25] X. H. Li, S. D. Deng, G. N. Mu, H. Fu, F. Z. Yang, Corros. Sci. 50 (2008) 420-430. [26] A. O. Dada, A. P. Olalekan, A. M. Olatunya, O. Dada, J. Appl. Chem. 3 (2012) 38-45. 2016 by the authors; licensee IAPC, Zagreb, Croatia. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/) http://creativecommons.org/licenses/by/4.0/