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International Journal of Corrosion
Volume 2013 (2013), Article ID 582982, 5 pages
Corrosion and Inhibition Effects of Mild Steel in Hydrochloric Acid Solutions Containing Organophosphonic Acid
1Department of Chemistry, Scope College of Engineering, Bhopal, Madhya Pradesh 462047, India
2Department of Chemistry, Dr. H.S. Gour University, Sagar, Madhya Pradesh 470003, India
Received 26 February 2013; Revised 22 June 2013; Accepted 23 July 2013
Academic Editor: Vesna Mišković-Stanković
Copyright © 2013 Manish Gupta 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.
A study has been made on the mechanism of corrosion of mild steel and the effect of nitrilo trimethylene phosphonic (NTMP) acid as a corrosion inhibitor in acidic medium, that is, 10% HC1 using the weight loss method and electrochemical techniques, that is, potentiodynamic and galvanostatic polarization measurements. Although corrosion is a long-time process, but it takes place at a faster rate in the beginning which goes on decreasing with due course of time. The above-mentioned methods of corrosion rate determination furnish an average value for a long-time interval. Looking at the versatility and minimum detection limit of the voltammetric method, the authors have developed a new voltammetric method for the determination of corrosion rate at short-time intervals. The results of corrosion of mild steel in 10% HC1 solution with and without NTMP inhibitor at short-time intervals have been reported. The corrosion inhibition efficiency of NTMP is 93% after 24 h.
Mild steel is a major material of construction. It is extensively used in chemical and allied industries for handling alkalis, acids, and salt solutions . Hydrochloric (HC1) acid is the solvent most often employed for chemical cleaning. It attacks a wide range of scales . Nitrogen compounds constitute the largest class of inhibitors for hydrochloric acid  solution. During the past decade a number of polymers and phosphonates have been used in different inhibitor compositions in aqueous and acid solutions . They form stable complexes and some times act as detergent also. The role of inhibitor is the prevention of the adsorption of aggressive anions and reduction of the dissolution rate of the passivating oxide. In the present paper we have studied the action and effectiveness of nitrilo trimethylene phosphonic acid (NTMP) as inhibitor for corrosion of carbon steel in (10% HCl) acid solution.
Most of the methods are proposed in the field of corrosion rate determination, but they furnish an average value for a long-time interval . Looking at the sensitivity and minimum detection limits [6, 7] of polarographic techniques, that is, direct current polarography (DCP), differential pulse polarography (DPP), and voltammetric, that is, differential pulse anodic stripping voltammetric (DPASV) method has been used to determine the corrosion rates and inhibition efficiency of NTMP of mild steel in 10% HC1 solution at short time intervals. Significantly it has also been possible to determine the corrosion rates simultaneously with respect to Fe(II) and Fe(III) which is not possible using other methods prevalent in the field. Their results have been discussed in the paper.
2.1. Chemicals and Reagents
All the chemicals used were of anal R/BDH grade. The inhibitor (NTMP, 99.9% pure) was synthesized at the Central Research Institute For Chemistry, Budapest, Hungery. Experiments were carried out in 10% HC1 solution. Mild Steel specimens mm size having composition (C-0.23%, P-0.05%, S-0.055%) were used in experiments. These specimen were polished following the usual procedure . All the measurements were carried out at room temperature 30°C.
2.2. Gravimetric Measurements
After abrasion with 600 grit papers all samples were degreased with acetone, pickled in 15% HC1 solution, washed under running tap water, rinsed in distilled water, dried with acetone, and weighed. The variation of solution corrosiveness and corrosion rate as a function of time was investigated using the planned interval test technique . Three weighed specimens were introduced into the solution. These were removed after various exposure times, giving damage factors referred to as for 22 h, for 3 h, and for 25 h. A fourth specimen () was introduced into the cell for the last period for 3 h. The values of , (measured values) and (calculated from , and ) relate to the same testing period, but under different conditions. This technique is schematically illustrated in Figure 1.
After each experiment, the specimens were cleaned by washing in water and acetone then weighed; from these measurements the corrosion rates were calculated. The methods of evaluating the results and combinations of situations are summarized in Table 1.
2.3. Potentiodynamic Polarization Measurement
The specimen was molded into epoxy resin in order to cover the sides of the rod, while the circular cross section area of the cylinder was exposed to the solution. The specimen was polished and washed with distilled water before the experiment. The potential scan path was 50 mV/5 min. The observed current was plotted against applied potential.
2.4. Galvanostatic Polarization Measurement
The galvanostatic polarization measurements were also made in 10% HC1 solution on 10 cm2 cylindrical surface of the working electrode. Saturated calomel electrode (SCE) was used as a reference electrode. An AJCO Electronics (model VT S5016) attached to a multiplex galvanometer was used for the galvanostatic studies. The polarization currents were measured by using a cycle of 10 s and changing potential by 10 mV. Both anodic and cathodic cycles were used alternately. The corrosion current density was plotted against the applied potential.
2.5. Voltammetric and Polarographic Measurements
An Elico Pulse Polarograph (model CL-90) was used for these studies. A cell consisting of three electrodes, namely, saturated calomel electrode as a reference, a coiled platinum wire as an auxiliary, and a dropping mercury electrode (for DCP and DPP)/glassy carbon fiber electrode (for DPASV) as a working electrode, was used. The test specimens were polished as discussed earlier, and one such specimen was suspended in 10% HCl solution at room temperature (25°C). Nitrogen gas was bubbled throughout the solution through the experiment to avoid the oxidation of dissolved Fe(II) to Fe(III). A definite aliquot of the solution was withdrawn from the test solution at different intervals (5, 10, 20 min, 1, 2, and 24 h), and polarograms and voltammograms were recorded in deaerated 0.1 M ammonium tartrate + 0.001% gelatin at pH . The pH of the test solution was adjusted using ammonia solution. A similar experiment was performed using 170 mg/L NTMP in 10% HC1 solution.
3. Results and Discussion
3.1. Gravimetric Measurement
The results of weight loss determination by gravimetric are shown as corrosion rates in the presence and absence of NTMP inhibitor in Table 1. The data obtained for the periods and suggest that solution corrosiveness increases in the base solution (10% HCl) while in the presence of NTMP it decreases (). The higher corrosivity of the solution can be attributed to the increase in concentration of iron ions in the solution. This suggests that NTMP molecules reduce the stimulating effect of iron ions. By comparison with the data relating to and it can be concluded that metal corrodibility decreases () as a function of time in the presence of the NTMP. This indicates that the formation of an inhibitor film requires some time; that is, the inhibition process has an induction period. The increased inhibition effect of NTMP may be explained on the argument that nitrogen of NTMP facilitates complex formation between metal ions coming out in the solution with NTMP and also the formation of complexed film at the metal surface.
3.2. Potentiodynamic Polarization Measurements
Figure 2 shows the results of potentiodynamic polarization measurements in the presence and absence of NTMP inhibitor in 10% HC1 solution. The curve clearly shows the cathodic and anodic inhibition properties of inhibitor. It is quite clear from the curves that the corrosion potentials are more positive (anodic) than the rest of potentials. The inhibitor shows a remarked effect in lowering the current. However, in the cathodic region the effect is not significant. Thus it could be conduced that NTMP affects the anodic part of the corrosion process. Thus they work as anodic protector.
3.3. Galvanostatic Polarization Measurement
Figure 3 depicts the galvanostatic polarization curves for the corrosion of mild steel in 10% HC1 solution with and without NTMP inhibitor. It is clear from the figure that both anodic and cathodic currents decrease in the presence of inhibitor. However, the corrosion potentials are shifted to more electropositive values with NTMP inhibitor, but the Tafel slopes of the curves remain almost the same. The shift in corrosion potential with NTMP is +50 mV. Thus, it could be concluded that the film formed by the inhibitor acts through the blocking effect, mainly on the anodic reaction.
3.4. Voltammetric and Polarographic Measurements
Figures 4(a), 4(b), and 4(c) are the direct current polarogram (DCP), differential pulse polarogram (DPP), and differential pulse anodic stripping voltammogram (DPASV) for corrosion sample after 5 min in 0.1 M ammonium tartrate and 0.001% gelatin at pH . The half-wave potential ()/peak potential () values for Fe(II) and Fe(III) are −0.81 V/−0.83 V and −1.23/−1.25 V, respectively, in DCP/DPP mode, and values are −0.4 V and −0.72 V for Fe(II) and Fe(III) in DPASV mode . Figure 5 shows the DPASV curves of corrosion mixtures of mild steel at different time intervals. These curves show that by using voltammetric and polarographic methods, it is possible to analyze the presence of Fe(II) and Fe(III) in the solution, simultaneously. Fe(II) and Fe(III) produce two separate well-defined polarographic peaks in each case. The wave height/peak height for Fe(II) and Fe(III) over the whole of the working concentration range in DCP, DPP, and DPASV modes is proportional to the Fe(II) and Fe(III) concentrations. The corrosion rates at different time intervals with respect to Fe(II) and Fe(III) are summarized in Table 2.
Figure 6 shows the DPASV curves for the corrosion solution to which NTMP (170 mg/L) has been added. A shift in the value for each of the Fe(II) and Fe(III) indicates the M: NTMP complex formation in the solution.
Since the shift in and values of Fe(III) is more than that of Fe(II) in complexed system, it could be concluded that Fe(III) is more reactive in complex formation with NTMP than Fe(II) . The corrosion rates in the presence of NTMP inhibitor have been tabulated in Table 3. A perusal of the data in Tables 1, 2, and 3 clearly shows that the rate of corrosion is very fast in the beginning of the experiment, which goes on decreasing with due course of time. The corrosion inhibition efficiency of NTMP is 55%, 69%, 75%, 81%, and 84% after 5, 10, 20 min, 1, and 2 h, and it becomes 93% after 24 h, respectively.
Thus, the inhibitive efficiency of NTMP (organophosphonic acid) will depend on the structure of the protective inhibitor film formed by the dissolved Fe(II) and Fe(III) species on the metal surface. The NTMP used as an inhibitor for the present study has the following structure:
The nitrogen atom acts as the reaction centre in the complexation reaction with the metal ions.
A comparison of the corrosion rate data as calculated by gravimetric, galvanostatic, potentiodynamic polarization, and voltammetric methods clearly speaks that NTMP is a good inhibitor for corrosion inhibition of mild steel in acidic medium, that is, 10% HC1.
From the above data and ongoing discussion, it could be concluded that polarographic and voltammetric methods give dependable results for corrosion rates with respect to each species appearing in the solution, that is, Fe(II) and Fe(III). It is also clear that the proposed polarographic/voltammetric methods are highly sensitive for corrosion rate determination at short-time intervals and that too with respect to each species present in the solution, which is otherwise not possible using methods prevalent in the field of corrosion rate determination [11, 12] and also in the field of trace analysis, namely, atomic absorption spectrometry (AAS).
Conflict of Interests
The authors, that is, Manish Gupta, Jyotsna Mishra, and K. S. Pitre declare that they do not have any conflict of interests regarding this paper.
The authors are thankful to the M. P. Council of Science and Technology (MPCST) Bhopal, for providing research fellowship.
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