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Corrosion Inhibition of Henna Extract on Carbon Steel with Hybrid Coating TMSM-PMMA in HCL Solution

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DOI: 10.4236/ojsta.2018.71001    403 Downloads   886 Views   Citations

ABSTRACT

Green inhibitors are promising alternatives to toxic corrosion inhibitors as they are environmentally safe substances, ecologically acceptable and renewable. In this research, the effect of green henna as an inhibitor existing in the coating of TMSM-PMMA and its electrochemical study were analyzed. The coating was produced by “sol-gel” method in order to protect the corrosion of low-carbon steel. TMSM hybrid cell was synthesized by hydrolysis and condensation, Metaacryloxypropyltrimethoxysilane and Tetraetylorthosilicate with 1:1 molar ratio and PMMA hybrid cell was produced by Methylmetaacrylate polymerization. Finally two cells were mixed in 1:1 weight ratio. The carbon steel substrates were prepared by dip coating method. SEM technique was applied for the microstructure evaluation of thin layers including different concentrations of henna extract. Adhesion of coating was analyzed by “Pull off” test. Additionally, the experimental results obtained in different concentrations of henna extract using electrochemical methods such as tafel polarization, electrochemical impedance spectroscopy indicating that coating with the concentration of 3% inhibitor had a high level of inhibition efficiency in 0.1 M HCL. The results of polarization tests signified that henna extract acts as a mixed inhibitor.

1. Introduction

Carbon steels play an important role in industrial environment because of their good mechanical and physical properties as well as low cost [1] . However, they are susceptible to get attacked while being applied in corrosive solutions including aggressive compounds like HCL. Corrosion is a devastative phenomenon occurring due to the chemical or electrochemical reaction of substance with its surrounded environment. There exists a wide variety of methods by which corrosion can be prevented by the means of inhibitors and coatings. Coatings prevent exchanging electrons in electrochemical reaction. Because of this mechanism, a protective layer is formed between the substrate and the aggressive medium [2] . Compounds which are practically beneficial for the protection of metals are extremely toxic and can result in cancer [3] . One of the appropriate ways for the surface protection of some materials could be by the use of hybrid organic-inorganic sol-gels which are considered as suitable option for this purpose [4] . Sol-gel coatings have high quality of flexibility, hydrophobic properties, anti-corrosion, transparency and suitable adhesion to the substrate. The combination of polysiloxan with siloxan and polymer constitute a hybrid coating contributing to the appropriate control of corrosion. The main role of these hybrid materials is production of a very thin layer having good yields and it does not permit oxygen to diffuse to the surface of the metal [5] [6] [7] [8] . When coverage of the coating has a defect, its corrosion protection properties will be boosted by the presence of active corrosion inhibitors [9] [10] [11] [12] .

When organic inhibitor is added into hybrid coating, it becomes compatible with the present coating contributing to cross linking and film formation. The mechanism of inhibition is through inhibitor incorporation in the film, moving and precipitating. This procedure results in the constitution of passivating effect while a defect has emanated. Researchers have focused on natural products, for most of the synthetic organic inhibitors have inevitable hazardous effects. One of the organic compounds named henna is known as corrosion inhibitor having some merits such as profusion and being eco-friendly, and nontoxic [13] . In particular, hybrid coatings produced by sol-gel method have both inorganic and organic properties. It is possible to acquire an extensive diversity of hybrid sol-gel-derived materials, since an array of precursors for constituting inorganic component such as metal alkoxides, organo (alkoxy) silanes, and nanoparticles is available [14] . On top of that, they are highly compatible with polymerizable groups. The main usage of these types of materials is as coating. In addition, they have been used as bulk materials. Hybrid coatings are made up of a dual polymer network, in which inorganic parts are bound to polymer chains [15] .

Polymeric mixture forming from the existing of PMMA results in improving the properties of organic-inorganic hybrid coating. The classification of these materials is based on their chemical bond characteristics, thus they are classified into two general categories. Category I is in relation with hybrid films, in which inorganic fragments and organic polymers in the hybrid coating form weak bonds of the types Van der Waals, hydrogen, or ionic interaction, whereas Category II has strong bonds such as covalent or ionic covalent chemical ones [16] [17] [18] [19] .

By the suitable selection of inorganic and organic parts and their compositions, fresh and versatile hybrid materials can be acquired [16] . Providing the link between the organic and inorganic parts is a main step. When the bonds between these two parts are covalent, hybrids properties will be enhanced. For example, the connection between organic and inorganic phases like trialkoxysilane and vinylic ligands constitutes an appropriate bond [20] [21] . One type of trialkoxysilane is 3 methacryloxypropyltrimethoxysilane (TMSM, also known as MPTS) which has photo-sensitivity to UV radiation, thus it is used in optical equipment [22] [23] [24] . By the formation of a polymer from TMSM and PMMA creating by UV radiation or by heat treatments, the refractive characteristic will rise [25] .

In the present research, an organic-inorganic coating was prepared from the processes namely; polymerization, hydrolysis and condensation reactions of TMSM-PMMA and henna extract. Carbon steel ST37 was applied as the substrate. The hybrid film structure, with the addition of inhibitors into its network, was studied using SEM. The efficiency of protective coatings in the presence and absence of inhibitors was evaluated using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS).

2. Experimental

2.1. Specimen preparation

Carbon steel (ST37) having nominal composition of 0.179% C, 0.165% Si, 0.439% Mn, 0.203% Cu, 0.034% S and Fe balance is used. It is cut into 2 × 2 × 0.2 cm dimensions used for electrochemical characterization. Specimens were mechanically abraded with 100, 200, 400, 600, 800, 1000 grades of emery papers, then degreased by acetone and hand washed with distilled water.

2.2. Solution Preparation

Corrosion electrolyte was obtained by mixing 4.2 ml of HCL 37% with 500 ml distilled water in order to prepare 0.1 M HCL.

2.3. Inhibitor Preparation

The hybrid layers were prepared by a sol-gel method constituted by the following components: TMSM (C10H20O5Si, Merck) and TEOS (C8H20O4Si, Merck) with the addition of MMA (C5H8O2, Merck) and the thermal initiator benzoyl peroxide (BPO-C14H10O4, Reagent). For the preparation of the hybrid organic-inorganic films a sol-gel method was employed. The formation of these hybrid coatings includes the chemical reactions such as hydrolysis of the alkoxide precursors, condensation leading to the formation of the inorganic phase (polysiloxane), and polymerization of the methylmethacrylate material. Figure 1 depicts the structures of the reagents used in the synthesis of the TMSM-PMMA coating.

First Step: 1.24 gr TMSM and 0.024 gr BPO were mixed for 15 min at room temperature. Then 1.04 gr TEOS was added slightly and mixed for approximately 15 min. The next stage was adding 5 ml ETOH and 100 µl HCL (0.01 M)

Figure 1. Molecular structure of the component of TMSM-PMMA coating [15] .

and finally the whole mixture was mixed for about 1 hour at room temperature. The solution of henna extract with the concentration of 1%, 3%, 6%, 9% was added to the solution of this step.

Second Step: 5 gr MMA and 0.12 BPO were mixed at room temperature for 30 min.

Third Step: For preparation of the sol-gel TMSM-PMMA 0.5 gr of the solution in the second step was mixed by the whole solution of the first step.

All the blending stages must be in the closed beaker. The specimens were immersed in the hybrid sol for 45 seconds, and then oven-dried for approximately 30 min at 75˚C. In the sol-gel method the inorganic phase was prepared by mixing TMSM and TEOS at 60˚C for 1 hour.

2.4. Electrochemical Measurements

Electrochemical experiments were carried out in a conventional three-electrode cell with a graphite as a counter electrode (CE), prepared specimens (ST37) as the working electrodes (WE) and a standard calomel electrode (SCE) was used as the reference electrode. Electrochemical measurements were organized at room temperature in HCL solution (0.1 M) using an electrochemical unit (model PARSTAT 2273). The potentiodynamic polarization curves were conducted from the −250 to +250 mv vs. OCP, at a sweep rate of 0.5 mV・s−1. Electrochemical impedance spectroscopy (EIS) was performed over a frequency range of 100 kHz - 10 MHz and peak-to-peak ac amplitude of 10 A・Cm・V. The condition of this test was the immersion of the specimens in 0.1 M HCL after the time of 0 h, 24 h, 72 h and 168 h.

3. Results and discussion

3.1. Electrochemical Characterization

Potentiodynamic polarization measurements of hybrid coating of TMSM-PMMA in the 0.1 M HCL solution were carried out and the results were compared with the polarization results of the condition in which henna extract of the concentrations 1%, 3%, 6%, 9% were added to the hybrid coating (Figure 2). The inhibition efficiency (IE%) was computed according to the Equation (1) [26] :

I E %= ( ( I 0 I ) / I 0 ) × 100 (1)

where, I0 is the corrosion current density of hybrid coating and I is the corrosion

Figure 2. Potentiodynamic polarization curves for hybrid coatings in the HCL 0.1 M with various henna extract concentrations and comparison with the bare metal.

current density of the mentioned coating in which different concentrations of the inhibitor are employed. The rate of corrosion was calculated based on the equation (2) [26] :

mpy = ( 0 .129 a I corr ) / n D (2)

where Icorr is the corrosion current density in µA/cm2, a is atomic weight of metal in gram, n is the number of lost electron and D is the density of metal in gr/cm3. Various parameters like current density (Icorr), corrosion potential (Ecorr) as well as cathodic and anodic tafel slope (βc and βa) were assessed from the tafel polarization curves and with the parameters computed from the Equations (1) and (2) all were recorded in Table 1.

According to table 1 and due to the fact that adding henna extract as an inhibitor in the PMMA (second step of coating preparation) had low efficiency in comparison with the time that it had been added to the TMSM (first step of coating preparation), henna extract was added to the TMSM for all the electrochemical tests. The results of the polarization measurements are given in Table 2.

If the difference in the value of E corr ( Δ E = E corr without inhibitor E corr with inhibitor ) is higher than 85 mV, the inhibitor can be categorized as cathodic or anodic inhibitor. Moreover, if the difference in value of Ecorr is lower than 85 mV, the inhibitor can be classified as a mixed inhibitor [26] [27] [28] . When an inhibitor is used, a noticeable shift takes place in the cathodic part of tafel curve, while a change in the anodic part is slight. Consequently, henna extract as an inhibitor could be categorized as a mixed-type kind which has a dominant effect in the cathodic part of the polarization curve. Thus, in this study henna extract has acted as a mixed inhibitor.

Table 1. Kinetic parameters of tafel polarization for carbon steel specimen by adding henna extract to PMMA in TMSM-PMMA coating.

aCorrosion Potential, bCorrosion Current, cCathodictafel slope, dAnodic tafel slope, eProtection Efficiency, fCorrosion Rate.

Table 2. Kinetic parameters of hybrid sol-gel thin films and their comparison with the bare metal in the 0.1 M HCL.

The βa and βc values decreased when the concentration of henna extract increased from 1% to 3%. However, adding the concentration of 6% and 9% increased the values of βc and βa. This happened because the layer formed was broken so fast [29] [30] .

By the use of corrosion current density, the mechanism of corrosion reactions could be assessed. In this study, the bare carbon steel specimen had a higher corrosion rate in comparison with the coated system. By applying TMSM-PMMA hybrid coating, a dramatic decline in the current density was noticed. The higher concentration of henna, the more reduction in anodic current densities. The results showed that the coating with 3% inhibitor had the lowest anodic current density [31] . This depicts the lower corrosion rate of the coated systems, which means that the substrate had been protected by the hybrid coating. The current density was to be lower when the addition of henna extract acted as an inhibitor. In the absence of inhibitor, the value of the current density was 4.11 µA/cm2.

By adding inhibitor, the current density became lower. This occurred when henna extract 1% was added where the value of current density reached 0.25 µA/cm2. The current density became lower and reaching 0.059 µA/cm2 with the addition of 3% henna extract. The phenomenon occurred because of the process of adsorption on metal surfaces [32] . The value of the current density affected the value of the corrosion rate. In the absence of inhibitor the rate of corrosion was 1.90 MPY, while this value decreased to 0.02 MPY with the addition of 3% henna extract inhibitor to the hybrid coating. When henna extract added to the amount of 6% and 9% in the coating system, the corrosion rate rose owing to breaking the layer formed on the metal. Hence, the maximum inhibition efficiency was achieved for TMSM-PMMA coating with 3% henna extract.

Electrochemical impedance was applied for the corrosion assessment over longer timescales. Typical Nyquist i.e. impedance for hybrid coatings of TMSM-PMMA with 3% henna extract after 0 h, 24 h, 72 h and 168 h immersion in the 0.1 MHCL was compared with coatings of TMSM-PMMA employed on the bare metal, and the results are shown in Figure 3 and Figure 4, respectively. 0 h is the initial time when the specimens were exposed to HCL 0.1 M solutions.

Figure 3. Nyquist plot of hybrid coating of TMSM-PMMA without henna extract after soaking in HCL 0.1 M solution for 0 h, 24 h, 72 h and 168 h.

Figure 4. Nyquist plot of hybrid coating of TMSM-PMMA with 3% henna extract after soaking in HCL 0.1 M solution for 0 h, 24 h, 72 h and 168 h.

In order to represent the response of the electrochemical behavior to EIS tests, an equivalent circuit shown in Figure 5 is the best option. The components of the equivalent circuit are solution resistance Rs, capacitance Cdl and polarization resistance Rp for defects in the coatings, and a capacitance Ccoat and Rcoat for the remainder of the coating layer regarded as intact (non-defective) [33] [34] [35] . The inhibition efficiency of TMSM-PMMA thin film without and with optimum henna extract content after 0 h, 24 h, 72 h and 168 h immersion in HCL 0.1 M solution was assessed by Rp and Cdl values in the impedance test. Values are depicted in Table 3, respectively.

The double layer capacitance (Cdl) was computed based on the Equation (3) [36] :

C dl = 1 / ( RP 2 ΠF max ) (3)

where Cdl, Rp and Fmax are double layer capacity, polarization resistance and frequency maximum, respectively. The value of inhibition efficiency of henna extract (IE%) was according to the Equation (4) [26] :

I E % = ( R c t R ˚ c t ) / R c t × 100 (4)

Rct is the polarization resistance of the hybrid coating while it includes henna as an inhibitor and R˚ct is the mentioned parameter in the absence of henna extract.

Figure 5. Equivalent circuits for hybrid coating in the absence and presence of 3% henna extract.

Table 3. Impedance parameters of hybrid coating in the absence and presence of 3% henna extract in the HCL 0.1 M solution after immersion of 0 h, 24 h, 72 h and 168 h.

The increase in the diameter of the semicircle (Rct) in the case of acid solution in the presence of inhibitor was perceived in figure 3 and figure 4, indicating a rise in the corrosion resistance of system. In practical, henna extract as an inhibitor rose the impedance. These observations confirm the results of the polarization measurements and the fact that the inhibitor had an increasing effect on the protection behavior of the hybrid coating.

Organic coatings capacitive reactance and resistance properties can also produce a time constant. Water and ions typically diffuse into an organic coating when a coated metal is submerged in an electrolyte, and change the coating dielectric properties. Water and ions also move inside a coating in response AC polarization. However, water and ion movement through (and in) a coating is restricted by coating morphology, producing a coating or pore resistance. Coating time constants can change with time, as electrolyte concentration in the coating changes. Figure 5 depicts the equivalent circuit for undoped/doped hybrid coating with 3% henna extract with two time constant. Data listed in Table 3 show that by adding inhibitor to the coating, the values of Rct rose, while Cdl decreased. If Rct is large, the corrosion rate of the system will be lowered. Hence, the inhibitor creates a high level of protection. The decrease in Cdl is because of an increase of double layer thickness [37] . Therefore the relationship between Rct and Cdl is inversely proportional [38] . In view of a decrease in local dielectric constant or rise in the density of electric double layer. The presence of henna extract modified the structure of the electric double layer by adsorption inhibitor molecules at the interface of a metal with a solution. By adding an inhibitor in different concentration, the double layer capacitance decreased based on the EIS analysis. Adsorption inhibitor on the metal surface formed a barrier layer to prevent electron transfer. Cdl minimum value occurred by addition of the 3% henna extract at 168 hour of immersion in acidic media and its value reached 0.0125 μF・cm−2. These results depicts that henna extract had a noticeable effect on the corrosion control of TMSM-PMMA coating on carbon steel substrate. Tafel test and impedance results confirm these descriptions.

3.2. Microstructure of hybrid coating

Figure 6 and Figure 7 show the scanning electron micrographs for hybrid coating of TMSM-PMMA thin layer with and without 3% henna extract before and after potentiodynamic polarization in HCL 0.1 M. By comparison of the SEM micrographs at the same magnifications for hybrid coating (with and without henna extract), it was observed that there were no traces of track on the surfaces of both specimens. After electrochemical tests, no corrosion was detected on the hybrid coatings including 3% henna extract. However, after potentiodynamic polarization the surface of the specimen without henna extract 3% as an inhibitor was not smooth. The cracks and pits shown in Figure 6(b) indicated corrosion in the media without henna extract as an inhibitor. According to Figure 6(b), the regions surrounding corrosion were damaged. Therefore usage of inhibitor in the micro structure of the coatings can highly control the corrosion of the substrates.

The data reported in Table 4 indicates that the strength of the bond between coating and substrate was increased in light of the inhibitor addition. Thus adhesion strength was enhanced by the presence of henna extract in the hybrid coating TMSM-PMMA. The chemical reaction between the components of

Figure 6. SEM images of hybrid coatings of TMSM-PMMA without henna extract before (a) and after (b) potentiodynamic tests in HCL 0.1 M solution.

Figure 7. SEM images of hybrid coatings of TMSM-PMMA with 3% henna extract before (a) and after (b) potentiodynamic tests in HCL 0.1 M solution.

Table 4. Pull-off adhesion test in dry condition.

henna inhibitor and (Fe2+) on carbon steel surface resulted in strengthening the bonds leading to the protection of the surface in aggressive environment.

3.3. Inhibition Mechanism

Henna leaves contain soluble matter Lawson (2-hydroxy-1, 4 naphthoquinone) resin and tannin, coumarins, gallic acid and Sterols shown in Figure 8 [39] . The amount of Lowsone in the henna leaves is 1.02% [40] . The coloring matter is quinine.

The inhibition performance of Tannins in alkaline media is higher in comparison with the acidic environments [40] [41] . The relatively higher amount of lawsone exits in the extract. Lawson molecule in the complex compound is a ligand and can constitute a chelate with a wide variety of metal cations. The inhibition mechanism is due to the reaction between substrate’s cations and lawsone molecule. Aromatic compounds include rotating π-electron which is exposed to electron of the acid solution [42] [43] [44] . The hydroxyl group contains a pair of electrons in lawsone molecule in the case of the reaction between acid solution and lawsone molecule and this pair of electrons is rotating in the aromatic ring in acid chloridric solution leading to the scheme shown in Figure 9 [45] [46] [47] . When hydrogen atom migrates to the adjacent carbon with its electrons, the binary bond position changes in the cycle and this rearrangement results in lawsone isomer. This isomer combines with Fe2+ cations presenting in carbon steel, thus this formed combination leads to the inhibition of carbon steel in acid chloridric environment. On top of that, henna extract omits the deficiency in coating rising the inhibition efficiency [39] [48] [49] [50] [51] .

4. Conclusions

The effect of henna extract as an inhibitor incorporated into sol-gel matrix TMSM-PMMA, was evaluated in HCL 0.1 M on carbon steel specimens. The results are as followings:

1) By employing henna extract, there was no trace of cracks and pits on the surface of the specimens covered by hybridorganic-inorganic thin film.

2) Hybrid coating TMSM-PMMA offers a thin barrier protection and by the addition of henna, the inhibition efficiency reaches higher than 95%.

3) SEM analyses for investigating the morphology of the sol-gel coatings with henna extract have shown that the uniformity of coating has not decreased by the addition of henna extract inhibitor.

4) Henna extract as an inhibitor could be categorized as a mixed-type kind which has a dominant effect in the cathodic part of the polarization curve.

Figure 8. Molecular structure of a) Lawsone; b) Gallic acid and c) Tannic acid [40] .

Figure 9. Process of π-electron rotating on the lawsone molecule [45] .

5) The TMSM-PMMA coating with 3% henna extract provided the maximum inhibition effect. This inhibitor could be a suitable and appropriate choice for the substitution of toxic inhibitors. Furthermore, it could be used as a desirable corrosion inhibitor.

6) The results achieved from SEM, potentiodynamic polarization and impedance measurement tests were all compatible.

Conflicts of Interest

The authors declare no conflicts of interest.

Cite this paper

Khoshkhou, Z. , Torkghashghaei, M. and Baboukani, A. (2018) Corrosion Inhibition of Henna Extract on Carbon Steel with Hybrid Coating TMSM-PMMA in HCL Solution. Open Journal of Synthesis Theory and Applications, 7, 1-16. doi: 10.4236/ojsta.2018.71001.

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