SciELO - Scientific Electronic Library Online

 
vol.61 issue3RESPONSIVE POLYMER HYBRID GEL CROSS-LINKED BY N,N-(1,2-DIHYDROXYETHYLENE) BISACRYLAMIDE FOR CATALYTIC APPLICATIONUV SPECTROPHOTOMETRIC DETERMINATION OF pK's OF 1,2,4-TRIAZOLINE-3-THIONES IN SODIUM HYDROXIDE SOLUTIONS author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Journal of the Chilean Chemical Society

On-line version ISSN 0717-9707

J. Chil. Chem. Soc. vol.61 no.3 Concepción Sept. 2016

http://dx.doi.org/10.4067/S0717-97072016000300012 

 

THE INHIBITION OF STEEL CORROSION IN ACIDIC SOLUTIONS BY A NEW SCHIFF BASE

 

N. K. BAKIRHANa,b*, A. ASANc, N. COLAKb, S. SANLId

a Department of Analytical Chemistry, Faculty of Pharmacy, Ankara University, 06100 Ankara, Turkey
b Hitit University, Science & Literature Faculty, Department of Chemistry,19100, Çorum, Turkey
c
Hitit University, Engineering Faculty, Department of Chemical Engineering,19030, Çorum, Turkey
d
Usak University, Science & Arts Faculty, Department of Chemistry, Usak, 64200, Turkey
* e-mail: nurgulk44@gmail.com


ABSTRACT

The inhibition effect of 2,2'- (((thiobis (4,1 phenylene)) bis(azanylylidene)) bis(methanylyidene)) bis(4-methoxyphenol) (BIS-IMIN) on the corrosion behavior of 304-stainless steel (SS) in 0.5 M HCl solution was studied by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques. SEM, FT-IR, 1H-NMR, 13C-NMR methods used for characterization of BIS-IMIN. Potentiodynamic polarization curves indicated that BIS-IMIN act as mixed type inhibitor. The adsorption of the inhibitor was more suited with the Langmuir adsorption isotherm and kinetic parameters Kads, ΔGads Ea , ΔHads, ΔSads were determined at room temperature. The results showed that BIS-IMIN performed well inhibiting effect for the corrosion of the SS.

Keywords: Corrosion inhibitors; Stainless steel; potentiodynamic polarization; Electrochemical impedance spectroscopy.


 

1. INTRODUCTION

Nowadays, steel has been currently used as important construction materials in industry [1]. The inhibition of steel in acidic mediums by different types of organic inhibitors has been extensively studied. The use of these inhibitors is one of the most practical methods for protecting against the corrosion and its popularity is increasing. The heterocyclic organic compounds which have especially electroactive groups (sulfur, oxygen, nitrogen) have excellent properties for inhibition of corrosion of steel in acidic medias [2-5].

Corrosion inhibition of organic compounds depend on adsorption mechanism on the metal surface. That adsorption mechanism occurs by following steps;

a) Electrostatic interaction between charged metal surface and charged inhibitor structure,
b) The interaction of unshared electron pairs of organic compounds with charged metal surface,
c) The interaction of π-electron with metal surface,
d) The combination of the (a-c) above steps [6, 7].

In this research, our aim is to investigation of the inhibition effect of BIS-IMIN on the corrosion behavior of SS in 0.5 M HCl solution and clarify its inhibition mechanism using Tafel polarization, electrochemical impedance spectroscopy. In addition to electrochemical studies, characterization of inhibited molecule was determined by SEM, FT-IR, 1H-NMR and 13C-NMR spectrums.

2. EXPERIMENTAL

4-(4-Aminophenylthio)benzenamine (1.08 g, 5 mmol) solution in ethanol (20 mL), 2-hydroxy-5-methoxybenzaldehyde (1.52 g, 10 mmol) in ethanol (30 mL) was added drop by drop, the solution was stirred for 3 h at 25 °C. The obtained precipitate was filtered and dried under the vacuum. The solution was filtered warmly to remove impurities, and then left for crystallization at 25 °C. Yield: 1.97 g (81%), melting point: 197-199 °C. C28H24N2O4S (484.15): Calc. C 69.40, H 4,99, N 5.78, O 13.21, S 6.62; found: 69.27, H 5.21, N 5.63, S 6.48. The chemical structure of the investigated compound is represented in Figure 1.

 

Fig. 1. The synthesis of BIS-IMIN molecule.

 

The immersed time and temperature effects (298-328 K) were investigated of the BIS-IMIN compound towards the corrosion of SS at 0.5 M HCl solution with or without inhibitors.

All solutions were prepared from analytical-grade chemicals and doubly distilled water. The chemical composition of working electrode SS: 18.18 % Cr, 8.48 % Ni, 2 % Mn, 0.75 % Si, 0.1 % N, 0.08 % C, 0.045 % P, 0.03 % S and remainder is Fe. SS was embedded in epoxy resin and its geometrical surface area is 1 cm2. SS cleaning procedure was performed by polishing with a series of emery papers up to 1200 grad, washed with acetone and distilled water to removing of unpurities. Than SS was immersed in test solution without and with known concentration of BIS-IMIN. The concentration effect of inhibitor was studied between 5.0×10-3 M to 5.0×10-5 M.

For electrochemical measurements, a three-electrode electrochemical cell was used. SS as working electrode, platinium as counter electrode and saturated calomel electrode (SCE) as a reference electrode were put in electrochemical cell. CHI 660B electrochemical analyzer was used for measurements. EIS measurements obtained at 105 to 10-2 Hz frequency range and 7 mV amplitude. All electrochemical experiments were performed without stirring at 25 °C. During the polarization measurement, the potential scan rate was used as 1.0 mVs-1

The 1H and 13C NMR spectra were performed on a Bruker AVANCE DPX NMR spectrometer operating at 400 and 101.6 MHz. The 1H and 13C NMR chemical shifts were measured using SiMe4 as an internal standard. Infrared absorption spectra were obtained from a Nicolet 6700 spectrometer in ATR and were reported in cm-1 units. Carbon, nitrogen and hydrogen analyses were performed on a LECO CHNS-932 analyzer. Melting points were measured on an Electro Thermal IA 9100 apparatus using a capillary tube.

Surface morphologies of electrodes and investigation of elemental analysis of surface were obtained by SEM coupled with an EDS detector and LEO 440 microscope.

3. RESULTS AND DISCUSSION

3.1. Effect of inbitior concentration

3.1.1. EIS

To investigate the effects of the inhibitor concentration on the impedance behavior of SS in acid solution have been studied. Nyquist diagrams are given in Fig. 2.

 

Fig. 2. Nyquist plots for SS in 0.5 M HCl solution in the absence (a)
and presence of 5×10-5 M (b), 1×10-4 M (c), 5×10-4 M (d), 1×10-3
M (e), 5×10-3 M (f) inhibitor at 298 K.

 

It is clear from these Figures that the impedance spectra obtained yields a semi circular shape. This shows the corrosion of the SS in 0.5 M HCl solution is mainly controlled by a charge transfer process [8, 9]. The charge transfer resistance (Rct) must be corresponding to the resistance between the metal and OHP (Outer Helmholtz Plane) [10]. Rct is calculated from the difference of lower and higher frequencies [11]. The double-layer capacitance (Cdl) is obtained from the maximum frequency at imaginary component of the impedance [12]:

The impedance results are given in Table 1. According to the results, the protection of SS surface from the corrosive media is succesfull with BIS-IMIN. In the electrochemical impedance spectroscopy, the inhibition efficiency (IE) is calculated using Rct as follows:

 

Table 1. Impedance data of SS in 0.5 M HCl without and with
addition of 5.0×103 M of inhibitors at 298 K.

 

In the equation 2, Rct and Rct(inh) are the charge transfer resistance values without and with BIS-IMIN in 0.5 M HCl, respectively. With BIS-IMIN concentration, the Rct values increased, while the Cdl values were decreased. Decreasing Cdl values are related to replacement of water molecules with organic molecules which are adsorbed on the SS surface, so that metal dissolution is blocked [13, 14]. As know that nitrogen atom in molecule can be easily protonated in acidic solutions [15]. This protonated nitrogen atom adsorbs on the positively charged iron surface in acidic media and then the anodic dissolution of iron follows these steps:

Fe + Cl- (FeCl-)ads (a)
(FeCl-)ads
(FeCl)ads + e- (b)
(FeCl)ads → (FeCl+) + e- (c)
FeCl+
Fe2+ + Cl- (d)

The cathodic hydrogen evolution follows the steps:

Fe + H+ (FeH+)ads (e)
(FeH+)ads +e- → (FeH)ads (f)
(FeH)ads +H+ +e- → Fe + H2 (g)

Electron donating groups on the molecules effect the electron density of structure such as S with donating groups increases the electron density on the nitrogen of the -C=N— group, resulting high inhibition efficiency [16].

3.1.2. Potentiodynamic polarization measurements

Polarization measurements have been studied to obtaine knowledge about the kinetics of the anodic and cathodic reactions. After 15 min of immersing the steel electrode in 0.5 M HCl solution without and with different concentrations BIS-IMIN, measurements have been carried out in the potential range (Ecorr ± 200 mV) at a scan rate of 1.0 mVs-1. The inhibition efficiency, IE%, at different BIS-IMIN concentrations was calculated from the polarization measurements using the Equation 3. [17], respectively.

where Io and Ii are the corrosion current densities for steel electrode in the uninhibited and inhi ibited solutions, respectively.

Fig. 3 shows the effect of BIS-IMIN concentration on the cathodic and the anodic polarization curves of steel in 0.5 M HCl. The polarization parameters calculated from these curves are illustrated in Table 2. Fig. 3 shows that increasing the BIS-IMIN concentration reduces both the cathodic and the anodic currents with a slight cathodic shift in the Ecorr values.

 

Fig. 3. Effect of inhibitor concentration on the potentiodynamic
polarization response for SS in 0.5 M HCl solution in the absence (a)
and presence of 5×10-5 M (b), 1×10-4 M (c), 5×10-4 M (d), 1×10-3
M (e), 5×10-3 M
(f) inhibitor at 298 K.

 

Table 2. Polarization parameters of steel corrosion in 0.5 M HCl
without and with addition of various concentrations of inhibitor.

 

According to the decreasing of concentration values and cathodic-anodic densities of BIS-IMIN, were decreased and this showed us BIS-IMIN is a mixed-type inhibitor. In the other way, addition of BIS-IMIN reduces anodic dissolution and cathodic hydrogen evolution reaction.

3.2. Adsorption isotherm

Chemical stuctures of organic molecules affect the adsorption process [18]. Temkin, Langmuir, Flory-Huggins, Bockris-Swinkels and Frumkin adsorption isotherms are studied and checked to find the best suitable isotherm for adsorption of BIS-IMIN molecule on the steel surface in the acid solution. Langmuir adsorption isotherm, which is given by Eq. (4) was found more suitable with an average correlation coefficient of 0.9999 (Fig. 4).

 

Fig. 4. Langmuir isotherm for the SS electrode in 0.5 M HCl
containing different concentrations of BIS-IMIN.

 

where C(inh) is inhibitor concentration, θ is the degree of the coverage on the metal surface and Kads is the equilibrium constant for the adsorption-desorption process [18]. The value of equilibrium constant, Kads calculated from the reciprocal of the intercept of isotherm line as 33.6 M-1. The high value of the adsorption equilibrium constant reflects the high adsorption ability of this BIS-IMIN on SS surface. The free energy of the adsorption of inhibitor on SS surface can be evaluated with the following equation;

where R is the gas constant and T is the absolute temperature. The constant value of 55.5 is the concentration of water in solution in mol/dm3. From Eq. (5), ΔGads was calculated as -18.66 kJmol-1. The negative value of ΔGads means spontaneous adsorption of the BIS-IMIN on the SS surface [19] and also the strong interaction between BIS-IMIN molecules and SS [20]. The value of ΔGads is less than 40 kJ mol-1 is commonly interpreted with the presence of physical adsorption by the formation of an adsorptive film with an electrostatic character [21, 22].

In physisorption process, it can be assumed that acid anions such as Cl- ions are adsorbed on the metal surface, donating an excess negative charge to the metal surface. In this way, cationic inhibitor molecule adsorbed on the negatively charged surface. This is also shown by other researchers [23, 24].

3.3. Effect of temperature

The effect of temperature on the inhibited acid-metal reaction is very complex, because many changes occur on the metal surface such as rapid etching and desorption of inhibitor and the inhibitor itself may undergo decomposition [25]. The change of the corrosion rate with the temperature was investigated in 0.5 M HCl, both in absence and presence of BIS-IMIN. Potantiodynamic polarization measurements were performed at different temperatures from 25 to 55 °C in absence (Fig. 5) and presence of 5×10-3 M of BIS-IMIN. (Fig. 6).

 

Fig. 5. Anodic and cathodic polarization curves for SS in
0.5 M HCl without inhibitor at different temperatures.

 

Fig. 6. Anodic and cathodic polarization curves for SS in 0.5 M HCl
with 5×103 M of BIS-IMIN at different temperatures.

 

By the Arrhenius equation, the apparent activation energy (Ea) of metal corrosion in both media (blank and inhibited) can be calculated" from the following equation [26]:

where A is the Arrhenius constant.

Fig. 7 shows the logarithm of icorr against the reciprocal of temperature in the absence and presence of BIS-IMIN. The Ea values of reactions on the electrode surfaces are calculated from the slope of lines at lnl versus 1000/T (K--1). The calculated value of Ea in the absence of inhibitor is 49.40 kJ/ mol, while in the presence of BIS-IMIN is 56.11 kJ/mol respectively. In the literatures, the higher Ea for corrosion process in the presence of an inhibitor is attributed to the physisorption of inhibitor [13].

 

Fig. 7. ln icorr vs 1000/T for SS dissolution in 0.5 M HCl in the
absence (a) and presence (b) 5×10-3 M of BIS-IMIN.

 

The heat of adsorption process (Qads) can be calculated from the variation of surface coverage versus reciprocal of temperature by using the Langmuir's adsorption isotherm as following [27]:

where A is a constant and Qads is the heat of adsorption and equal to enthalpy of adsorption process (ΔHºads) with good approximation.

Fig. 8 represents the variation of log [θ/(1- θ)] versus 1/T for inhibitor molecule. The heat of adsorption can be found from the slope of the lines, which are equal to (-Qads/2.303 R). The entropy of adsorption process (Δads) can be calculated based on the following thermodynamic basic equation [28]

 

Fig. 8. log (θ/1- θ) vs 1000/T for adsorption BIS-IMIN
molecule.

 

The heat of adsorption (Qads) and the entropy value of the inhibitor adsorption (ΔSads) were calculated as -7.51 kJmol-1 and 37.4 Jmol-1 K-1, respectively. The negative AHads value means that the exothermic reaction is occurred in solution between the SS suface and corrosive media. this reaction is explained as inhibitor compound adsorbs on metal surface and at the same time water molecule desorbs from the metal surface [29]:

where Org(sol) and Org(ads) are the organic compound which dissolved in the aqueous solution and adsorbed onto the metallic surface, respectively, H2O(ads) is the water molecule adsorbed on the metallic surface and x is the size ratio representing the number of water molecules replaced by one organic adsorbate.

Adsorption of organic compounds on the metal surface causes a decrease in randomness, hence in ΔSads. The desorption of water molecules causes a increase in disorderness. Thermodynamic parameters are total of the adsorption of organic compounds and desorption of water molecules. If the positive sign ΔSads is obtained, it shows that the increase of solvent entropy [30]. In the other way, disorderness increases with the desorption of water molecules from the metal surface by one organic compound [6].

3.4. FTIR Analysis

The Schiff base reaction of 4-(4-aminophenylthio) benzenamine with 2-hydroxy-5-methoxybenzaldehyde in a 1:2 ratio which was mixed. This newly synthesized Schiff base compound. The main IR bands (Fig. 9) Ar-H at 3070 cm-1, CH=N at 1613 cm-1 was observed.

 

Fig. 9. 1H NMR spectrum of BIS-IMIN molecule.

 

1H-NMR (Fig. 10) and 13C-NMR (Fig. 11) data of Schiff base compound in deutero form of DMSO were collected. The integration was observed which was in accordance with, 1:2 formulations proposed. -OCH3 was observed at 3.75 ppm, the multiply peaks observed at 6.91 and 7.25 ppm were assigned to aromatic ring protons respectively. The singlet at 8.94 ppm was assigned to CH=N protons, and the singlet at 12.27 ppm was assigned Ar-OH proton. The 13C-NMR spectra data of compound was also in accord with the proposed structure. The elemental analyses was compatibility to proposed structural.

 

Fig. 10. 13C NMR spectrum of BIS-IMIN molecule.

 

Fig. 11. The SEM images and their corresponding EDX analysis of the stainless steel
surface: (a) and (b) belong to the steel corroded in 0.5 M HCl without inhibitor, (c)
and (d) correspond to the working steel electrode exposed to the acid in the
presence of the BIS-IMIN inhibiting molecule.

 

IR (ATR cm-1): 3070 (Ar-H), 1613 (CH=N) ;1H NMR (d6-DMSO, ppm): 3.75 (s, 3H, OCH3), 6.91 (d, 2H, Ar-H), 7.05 (dd, 1H, Ar-H), 7.25 (d, 1H, Ar-H), 8.94 (s, 1H, CH=N), 12.27 (s, 1H, Ar-OH); 13C NMR (d6-DMSO, ppm): 56, 115, 117, 119, 121, 123, 127, 132, 133, 136, 148, 152, 154,163.

3.5. SEM Analysis

SEM images and the EDS analysis obtained from SS surface after specimens immersion in 0.5 M HCl solutions for 2 days in the absence and presence of 5.0×10-3 M of BIS-IMIN.

After 2 days immersion in 0.5 M HCl without the BIS-IMIN, the morphology of SS is shown in Fig. 11a, which is typical corrosive attack on a surface with diverse features and rugosity apparent. The accompanying EDX analysis, shown in Fig. 11c, naturally revealed the presence of the main Cl peak, apart from the peaks corresponding to Fe. Fig. 11b is the morphology that resulted after testing in 0.5 M HCl in the presence of the 5.0×10-3 M inhibitor. Although the resulting morphology apparently looks similar to the previous one, the main difference is given by the EDX spectrum, see Fig. 11d, which bears very small Cl peak, thus suggesting that the BIS-IMIN molecule has adsorbed on steel surface, which is responsible for the inhibition of corrosion. There is much less corrosion product at the electrode surface.

4. CONCLUSION

In the present work, electrochemical impedance spectroscopy, potentiodynamic polarization methods were used to study the protection performance of BIS-IMIN to inhibit the corrosion of mild steel in 0.5 M HCl solutions at 25 °C.

The following are the main conclusions of this study:

This molecule reduced significantly the corrosion of mild steel in 0.5 M HCl. BIS-IMIN is suitable inhibitor for SS in 0.5 M HCl solution and its efficiency increase with increasing concentration values. EIS plots indicated that the addition of inhibitors increases the charge-transfer resistance of the corrosion process. Polarization curves demonstrated that this molecule was of mixed-type inhibitor for SS corrosion in these acid solutions. Corrosion current density is increased by increasing the temperature, but, the rate of its increase is lower at the presence of BIS-IMIN. This schiff base is adsorptive inhibitor and its adsorption obeys the Langmuir's adsorption isotherm. Thermodynamic adsorption parameters such as ΔGads, ΔHads and ΔSads, show that BIS-IMIN are r r ads ads ads' adsorbed by a spontaneous exothermic process.

ACKNOWLEDGMENTS

The authors are grateful to Hitit University BAP unit for financial support to the project number of FEF03.11.006.

 

5. REFERENCES

1.- M. A. Migahed, M. Abd-El-Raouf, A. M. Al-Sabagh, Electrochim Acta 50, 4683, (2005)        [ Links ]

2.- A. V. Shanbhag, T. V. Venkatesha, R. A. Prabhu, J Appl Electrochem 38, 279, (2008)        [ Links ]

3.- E. Machnikova, K. H. Whitmire, N. Hackerman, Electrochim Acta 53, 6024, (2008)        [ Links ]

4.- K. F. Khaled, Electrochim Acta 53, 3484, (2008)        [ Links ]

5.- M. Sahin, G. Gece, F. Karci, J Appl Electrochem 38, 809, (2008)        [ Links ]

6.- E. Naderi, A. H. Jafari, M. Ehteshamzadeh, M. G. Hosseini, Mater Chem Phys 115, 852, (2009)         [ Links ]

7.- F. Bentiss, M. Lagrenee, M. Traisnel, J. C. Hornez, Corros Sci 417, 89, (1999)        [ Links ]

8.- M. E. Achouri, S. Kertit, H. M. Gouttaya, B. Nciri, Y. Bensouda, L. Perez, M. R. Infante, K. Elkacemi, Prog Org Coat 43, 267, (2001)        [ Links ]

9.- A. Chetouani, A. Aouniti, B. Hammouti, N. Benchat, T. Benhadda, S. Kertit, Corros Sci 45, 1675, (2003)        [ Links ]

10.- R. Solmaz, G. Kardas, M. Culha, B. Yazici, M. Erbil, Electrochim Acta 53, 5941, (2008)        [ Links ]

11.- T. Tsuru, S. Haruyama, B. Gijutsu, J Jpn Soc Corros Eng 27, 573, (1978)         [ Links ]

12.- L. Elkadi, B. Mernari, M. Traisnel, F. Bentiss, M. Lagrenee, Corros Sci 42, 703, (2000)        [ Links ]

13.- F. Bentiss, M. Lebrini, M. Lagrenee, Corros Sci 47, 2915, (2005)         [ Links ]

14.- W. Li, Q. He, C. Pei, B. Hou, Electrochim Acta 52, 6386, (2007)         [ Links ]

15.- A. Yurta, A. Balaban, S.U. Kandemir, G. Bereket, B. Erk, Mater Chem Phys 85, 420, (2004)        [ Links ]

16.- J. Fang, J. Li, J Mol Struct (Theochem.) 593, 179, (2002)        [ Links ]

17.- S. S. Abd El-Rehim, H. H. Hassan, M. A. Amin, Corros Sci 46, 5, (2004)        [ Links ]

18.- A. K. Maayta, N. A. F. Al-Rawashdeh, Corros Sci 46, 1129, (2004)         [ Links ]

19.- L. Tang, X. Li, L. Li, G. Mu, G. Liu, Mat Chem Phys 97, 301, (2006)         [ Links ]

20.- S. Kertit, B. Hammouti, Appl Surf Sci 93, 59, (1996)        [ Links ]

21.- G. Moretti, F. Guidi, G. Grion, Corros Sci 46, 387, (2004)        [ Links ]

22.- O. K. Abiola, N. C. Oforka, Mater Chem Phys 83, 315, (2004)        [ Links ]

23.- A. Popova, M. Christov, S. Raicheva, E. Sokolova Corros Sci 46, 1333, (2004)        [ Links ]

24.- G. Bereket, E. Hur, C. Ogretir, Molecular Struc (Thochem) 578, 79, (2002)        [ Links ]

25.- S. Ashry, A. Nemr, S. A. Essawy, S. Ragab, Prog in Org Coat 61, 11, (2008)        [ Links ]

26.- E. A.Noor, A. H. Al-Moubaraki, Mater Chem and Phys 110, 145, (2008)        [ Links ]

27.- R. Solmaz, G. Kardas, M. Culha, B. Yazici, M. Erbil, Electrochim Acta 53, 5941, (2008)        [ Links ]

28.- S. M. A. Hosseini, A. Azimi, Corros Sci 51, 728, (2009)        [ Links ]

29.- G. Avci, Colloids and Surfaces A: Physicochem and Eng Aspects 317, 730, (2008)        [ Links ]

30.- M. M. Saleh, Mater Chem Phys 98, 83, (2006)        [ Links ]

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License