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International Journal of Modern Engineering Research (IJMER)
www.ijmer.com Vol. 3, Issue. 4, Jul - Aug. 2013 pp-2456-2459 ISSN: 2249-6645
www.ijmer.com 2456 | Page
S. Ananth Kumar1
, A. Sankar1
, M. Vijayan2
, S. Ramesh Kumar3
1
Kandaswami Kandar's College, P. Velur, Namakkal-638 182, India
2
Scientist, centre for conducting polymers, Electrochemical materials science division, Central Electrochemical research
Institute,
Karikudi-630006, India
3
PSG College of Technology Peelamedu, Coimbatore 641 004, India
Abstract: The corrosion inhibitive action of oxystelma esculentum stem on mild steel corrosion in 0.5 M H2SO4 solution
was studied using weight loss method, potentiodynamic polarization and EIS measurements. The results obtained indicate
that the extracts functioned as good inhibitors in 0.5 M H2SO4 solution. Inhibition efficiency was found to increase with
extract concentration. The adsorption of constituents in the plant extract on the surface of the metal is proposed for the
inhibition behavior.
Key words: Inhibitor, Mass loss, Impedance, Polarization, oxystelma esculentum
I. Introduction
Corrosion inhibitors are widely used in industry to reduce the corrosion rate of metals and alloys in contact with
aggressive environments. Most of the corrosion inhibitors are synthetic chemicals, expensive, and very hazardous to
environments. Therefore, it is desirable to source for environmentally safe inhibitors [1-3]. There are some reports on the
inhibition effects of non-toxic compounds on the Corrosion of metals. We have recently reported the inhibition effect of
amino acids on the steel [1] and aluminum [4] corrosion in acidic media. The rare earth metals have been proposed as
corrosion inhibitors [5-8]. The inhibition effects of some non-toxic organic compounds have been also reported for steel
corrosion [9, 10] but they are expensive. The aim of this study was to investigate the inhibition effect of Oxystelma
esculentum extract as a cheap, raw and non-toxic corrosion inhibitor on mild steel corrosion in 0.5M H2SO4. The
electrochemical measurements were used to evaluate the inhibition efficiencies.
II. MATERIAL AND METHODS
2.1 Preparation of oxystelma esculentum extract:
An aqueous extract of oxystelma esculentum stem extract was prepared by grinding 5g of plant stem, with distilled
water, filtering the suspending impurities, and making up to 100 ml. The extract was used as corrosion inhibitor in the
present study.
2.2 Preparation of specimens
Carbon steel specimens (0.022% S, 0.038% Mn, 0.027%P, 0.086 C) of dimension 1.0 cm *4.0cm*0.2cm were
polished to a mirror finished with the emery sheets of various grades and degreased with trichloroethylene.
2.3 Weight loss method.
Carbon steel specimens in triplicate were immersed in 100 mL of the inhibited and uninhibited 0.5M H2SO4
solutions in the presence and absence of KI for two hours. The weight of each specimen before and after immersion was
determined using shimadzu balance, model Ay 62.The inhibition efficiency (IE) was then calculated using the expression;
I
Where W1and W2 are the corrosion rates in the absence and presence of the inhibitor, respectively.
2.4 Electrochemical impedance measurements
The impedance measurements were performed using a computer –controlled potentiostat (model Solartron SI-1260)
and the data were analyzed using gain phase analyser electrochemical interface (Solartron SI-1287). A three electrode set
up was employed with Pt foil as the auxiliary electrode and a saturated calomel electrode as the reference electrode. The
Teflon coated mild steel rod, with the surface prepared as described in the weight loss experimental method, served as the
working electrode. The measurements were carried out in the frequency range 106
–10−2
Hz at the open circuit potential by
superimposing sinusoidal AC signal of small amplitude, 10 mV, after an immersion period of 30 min in the corrosive media.
The double layer capacitance (Cdl) and charge transfer resistance (Rct) were obtained from the impedance plots as described
elsewhere11. Because Rct is inversely proportional to corrosion current density, it was used to determine the inhibition
efficiency (IE%) using the relationship;
OXYSTELMA ESCULENTUM Stem Extracts as Corrosion
Inhibitor for Mild Steel in Acid Medium
International Journal of Modern Engineering Research (IJMER)
www.ijmer.com Vol. 3, Issue. 4, Jul - Aug. 2013 pp-2456-2459 ISSN: 2249-6645
www.ijmer.com 2457 | Page
Where Rct and R0
ct are the charge transfer resistance values in the inhibited and uninhibited solutions respectively.
2.5. Polarization measurements
The potentiodynamic polarization curves were recorded using the same cell setup employed for the impedance
measurements. The potentials were swept at the rate of 1.66mV/s, primarily from a more negative potential than Eocp to a
more positive potential than Eocp through Ecorr. The inhibition efficiencies were calculated using the relationship 12;
Where I0
corr and Icorr are the corrosion current densities in the absence and in the presence of inhibitor, respectively
III. RESULTS AND DISCUSSION
3.1 Analysis of results of mass loss method
The corrosion rates and inhibition efficiency values, calculated using weight loss data, for various concentrations of
oxystelma esculentum extract in the presence and absence of KI the corrosion of carbon steel in 0.5M H2SO4 solution are
presented in Table.1. It is apparent that the inhibition efficiency increased with the increase in inhibitor concentration in the
presence and absence of KI . This behavior can be explained based on the strong interaction of the inhibitor molecule with
the metal surface resulting in adsorption. The extent of adsorption increases with the increase in concentration of the
inhibitor leading to increased inhibition efficiency. The maximum inhibition efficiency was observed at an inhibitor
concentration of 100 ppm. Generally, inhibitor molecules suppress the metal dissolution by forming a protective film
adsorbed to the metal surface and separating it from the corrosion medium. The corrosion suppressing ability of the inhibitor
molecule originates from the tendency to form either strong or weak chemical bonds with Fe atoms using the lone pair of
electrons present on the O and  electrons in benzene ring. It is also seen from table.1 that the leaf extract of oxystelma
esculentum at 25 ppm and 100 ppm concentrations shows 55.55 % and 66.00 % inhibition efficiencies respectively, Then
the values increased to 80.14 % after adding 25 ppm of KI solution in 0.5M H2SO4 solutions containing 100 ppm of
plant extract respectively. This showed a good synergistic effect between oxystelma esculentum extract and KI.
Table1.Corrosion rate (CR) of mild steels in 0.5M H2SO4 solutions the absence and presence of inhibitor and the
inhibition efficiency (IE) obtained by weight loss method.
. Inhibitor concentration
(ppm)
KI (0) ppm
CR
(mg cm-2
h-1
)
IE
%
0 136.00 -
10 65.42 51.90
25 58.26 57.16
50 46.06 66.13
75 41.26 69.66
100 37.75 72.24
3.2 INFLUENCE OF KI ON THE INHIBITION EFFICIENCY OF STEM EXTRACTS
Inhibitor concentration
(100ppm)
KI (25) ppm
CR
(mg cm-2
h-1
)
IE %
100 24.26 82.16
3.3 Electrochemical impedance spectroscopic measurements (EIS)
Impedance spectra obtained for corrosion of mild steel in 0.5 M H2SO4 contains a semicircle, representing the
interaction of metal surface with the corrosive environment.. The -R(CR) model best describes this situation. The semicircle
in the impedance plots contain depressed semicircles with the centre below the real axis. The size of the semicircle increases
with the inhibitor concentration, indicating the charge transfer process as the main controlling factor of the corrosion of mild
steel. It is apparent from the plots that the impedance of the inhibited solution has increased with the increase in the in which
International Journal of Modern Engineering Research (IJMER)
www.ijmer.com Vol. 3, Issue. 4, Jul - Aug. 2013 pp-2456-2459 ISSN: 2249-6645
www.ijmer.com 2458 | Page
the second one represents the interaction of metal surface with the corrosive environment. The first semicircle represents the
nature of the corrosive media .Since the conductivity of the corrosive medium is very low, this also behaves like a leaky
capacitor. The CR-CR model best describes this situation. The second semicircle in the impedance plots contain depressed
semicircles with the centre below the real axis. The size of the semicircle increases with the inhibitor concentration,
indicating the charge transfer process as the main controlling factor of the corrosion of mild steel. It is apparent from the
plots that the impedance of the inhibited solution has increased with the increase in the concentration of the inhibitor. The
experimental results of EIS measurements for the corrosion of mild steel in 0.5 M H2SO4 in the absence and presence of
inhibitor are given in Table 3. Said that sum of charge transfer resistance (Rct) and adsorption resistance (Rad) is equivalent
to polarization resistance (Rp).
Table 3. Impedance parameters obtained from electrochemical impedance studies.
Inhibitor
concentration
ppm
Rct
Ohm cm2
Cdl
µF
IE%
0 17.2 9.2578×10-6
-
100 63.00 2.5275×10-6
73.00
100+ 25ppmKI 104 1.5311×10-6
83.50
3.4 Potentiodynamic Polarization studies :
Fig 2. Potentiodynamic polarization curves of mild steel immersed in 0.5M H2SO4 solution in the absence and
presence of inhibitors
International Journal of Modern Engineering Research (IJMER)
www.ijmer.com Vol. 3, Issue. 4, Jul - Aug. 2013 pp-2456-2459 ISSN: 2249-6645
www.ijmer.com 2459 | Page
Table 4. Corrosion parameters in the presence and absence of inhibitor obtained from polarization measurements.
Inhibitor
concentration
ppm
-Ecorr
(mV)
βc
(mV/)
βa
(mV)
Icorr×10*6
µA
IE%
0 447 127 68 1.35
100 450 173 72 0.378 72.0
100+25ppmKI 453 195 94 0.278 82.4
The polarization curves obtained for the corrosion of mild steel in the inhibited (100 ppm) and uninhibited 0.5 M
H2SO4 solutions in the absence and presence of KI are shown in Fig.2. Electrochemical parameters such as corrosion
potential (Ecorr), corrosion current density (Icorr), cathodic and anodic tafel slopes (βc and βa ) and percentage inhibition
efficiency according to polarization studies are listed in table 4. Here Icorr decreased with increasing inhibitor concentration.
From the figures, it can be interpreted that the addition of this inhibitor to corrosive media changes the anodic and cathodic
tafel slopes. The changes in slopes showed the influence of the inhibitor both in the cathodic and anodic reactions. However,
the influence is more pronounced in the cathodic polarization plots compared to that in the anodic polarization plots. Even
though βc and βa values (table.3) change with an increase in inhibitor concentrations, a high βc value indicates that the
cathodic reaction is retarded to a higher extent than the anodic reaction13
.
From Fig.2 it is also clear that the addition of the inhibitor shifts the cathodic curves to a greater extent toward the
lower current density when compared to the anodic curves. The Ecorr value is also shifted to the more negative side with an
increase in the inhibitor concentration. These shifts can be attributed to the decrease in the rate of the hydrogen evolution
reaction on the mild steel surface caused by the adsorption of the inhibitor molecule to the metal surface14
. It has been
reported that a compound can be classified as an anodic and cathodic type inhibitor on the basis of shift of Ecorr value. If
displacement of Ecorr value is greater than 85 mv, towards anode or cathode with reference to the blank, then an inhibitor is
categorized as either anodic or cathodic type inhibitor otherwise inhibitor is treated as mixed type15,16
. In our study,
maximum displacement in Ecorr value was around 6 mV, indicating the inhibitor is a mixed type and more anodic nature and
does not alter the reaction mechanism. The inhibition effect has occurred due to simple blocking of the active sites, thereby
reducing available surface area of the corroding metal17,18
. The increase in inhibitor efficiency of inhibited (10mL) 0.5M
H2SO4 solution for the corrosion of mild steel after adding 25 ppm KI shows synergism between inhibitor molecules and KI.
IV. CONCLUSIONS
Results obtained from both electrochemical methods showed that the oxystelma esculentum stem acts as an
inhibitor for corrosion of steel in 0.5 M H2SO4 media. Corrosion inhibition action of oxystelma esculentum stem increased as
its concentration increases. Inhibition of steel in 0.5 M H2SO4 solution by oxystelma esculentum stem is attributed to
adsorption of the phytochemical compounds in this extract.
ACKNOWLEDGEMENTS
The authors generously acknowledge the support by Dr.R.Somasundaram M.D Dr. R. Arul M.Sc., Ph.D.,
Dr.S.Vedanayaki M.Sc.,Ph.D.,President ,Principal and head of the department chemistry respectively of kandaswami
Kandar’s college,P.Velur for providing necessary chemical and lab facilities to carry out chemical studies
References
[1] H. Ashassi-Sorkhabi, M. R. Majidi and K. Seyyedi, Applied Surface Science,225(2004)176
[2] A.Y. El-Etre, Corrosion Science,45(2003)2485
[3] A.Y. El-Etre, Corrosion Science,40 (1998)1845
[4] H. Ashassi-Sorkhabi, Z. Ghasemi and D. Seifzadeh, Applied Surface Science,249 (2005)408
[5] M. Bethencourt, F.J. Botana, J.J. Calvino and M. Marcos,Corrosion Science,40(1998)1803
[6] S. Virtanen, M.B. Ives, G.I. Sproule, P. Schmuki and M.J. Graham, Corrosion Science,39(1997)1897.
[7] B. Davó and J.J. de Damborenea, Electrochimica Acta,49(2004)4957
[8] A. Aballe, M. Bethencourt, F. J. Botana and M. Marcos, Journal of Alloys and Compounds, 323-324(2001)855
[9] K. C. Emregül and M. Hayvalı, Materials Chemistry and Physics,83(2004)209
[10] S. A. Abd El-Maksoud, Electrochimica Acta,49(2004) 4205
[11] Ashassi-Sorkhabi.H,.Shaabani.B,Seifzadeh.D, Electrochim. Acta,2005 ,50 ,3446.
[12] Shahin.M, Bilgie.S, Yilmaz.H, Appl. Surf. Sci.2003,195, 1
[13] Silverman D. C., "Practical Corrosion Prediction Using Electrochemical Techniques", ch. 68 in Uhlig's Corrosion Handbook,
2nd
edition (Revie,.R.W, ed.), The Electrochemical Society, 2000.
[14] Prabhu., T.V. Venkatesha, A.V. Shanbhag. Praveen. B.M, Kulkarni. G.M,.Kalkhambkar R.G, Mater. Chem. Phys. 2008,108 , 283
[15] Sanghvi. R.A, M.J., et al., Bull. Electrochem.1999, 13, 358.
[16] Felicia Rajammal Selvarani, S.Santhanalakshmi, J. Wilson sahayaraja, A. John Amalraj,and Susai Rajendran , Bull.
Electrochemistry.2004, 20 , 561-565.
[17] Susai RajendranS. Mary Reenkala, Noreen Anthony and Ramaraj,R. Corros Sci,2002, 44, 2243-2252.
[18] Scully. J. R., "Polarization Resistance Method for Determination of Instantaneous Corrosion Rates", Corrosion, Vol.2000,56, p.
199.

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OXYSTELMA ESCULENTUM Stem Extracts as Corrosion Inhibitor for Mild Steel in Acid Medium

  • 1. International Journal of Modern Engineering Research (IJMER) www.ijmer.com Vol. 3, Issue. 4, Jul - Aug. 2013 pp-2456-2459 ISSN: 2249-6645 www.ijmer.com 2456 | Page S. Ananth Kumar1 , A. Sankar1 , M. Vijayan2 , S. Ramesh Kumar3 1 Kandaswami Kandar's College, P. Velur, Namakkal-638 182, India 2 Scientist, centre for conducting polymers, Electrochemical materials science division, Central Electrochemical research Institute, Karikudi-630006, India 3 PSG College of Technology Peelamedu, Coimbatore 641 004, India Abstract: The corrosion inhibitive action of oxystelma esculentum stem on mild steel corrosion in 0.5 M H2SO4 solution was studied using weight loss method, potentiodynamic polarization and EIS measurements. The results obtained indicate that the extracts functioned as good inhibitors in 0.5 M H2SO4 solution. Inhibition efficiency was found to increase with extract concentration. The adsorption of constituents in the plant extract on the surface of the metal is proposed for the inhibition behavior. Key words: Inhibitor, Mass loss, Impedance, Polarization, oxystelma esculentum I. Introduction Corrosion inhibitors are widely used in industry to reduce the corrosion rate of metals and alloys in contact with aggressive environments. Most of the corrosion inhibitors are synthetic chemicals, expensive, and very hazardous to environments. Therefore, it is desirable to source for environmentally safe inhibitors [1-3]. There are some reports on the inhibition effects of non-toxic compounds on the Corrosion of metals. We have recently reported the inhibition effect of amino acids on the steel [1] and aluminum [4] corrosion in acidic media. The rare earth metals have been proposed as corrosion inhibitors [5-8]. The inhibition effects of some non-toxic organic compounds have been also reported for steel corrosion [9, 10] but they are expensive. The aim of this study was to investigate the inhibition effect of Oxystelma esculentum extract as a cheap, raw and non-toxic corrosion inhibitor on mild steel corrosion in 0.5M H2SO4. The electrochemical measurements were used to evaluate the inhibition efficiencies. II. MATERIAL AND METHODS 2.1 Preparation of oxystelma esculentum extract: An aqueous extract of oxystelma esculentum stem extract was prepared by grinding 5g of plant stem, with distilled water, filtering the suspending impurities, and making up to 100 ml. The extract was used as corrosion inhibitor in the present study. 2.2 Preparation of specimens Carbon steel specimens (0.022% S, 0.038% Mn, 0.027%P, 0.086 C) of dimension 1.0 cm *4.0cm*0.2cm were polished to a mirror finished with the emery sheets of various grades and degreased with trichloroethylene. 2.3 Weight loss method. Carbon steel specimens in triplicate were immersed in 100 mL of the inhibited and uninhibited 0.5M H2SO4 solutions in the presence and absence of KI for two hours. The weight of each specimen before and after immersion was determined using shimadzu balance, model Ay 62.The inhibition efficiency (IE) was then calculated using the expression; I Where W1and W2 are the corrosion rates in the absence and presence of the inhibitor, respectively. 2.4 Electrochemical impedance measurements The impedance measurements were performed using a computer –controlled potentiostat (model Solartron SI-1260) and the data were analyzed using gain phase analyser electrochemical interface (Solartron SI-1287). A three electrode set up was employed with Pt foil as the auxiliary electrode and a saturated calomel electrode as the reference electrode. The Teflon coated mild steel rod, with the surface prepared as described in the weight loss experimental method, served as the working electrode. The measurements were carried out in the frequency range 106 –10−2 Hz at the open circuit potential by superimposing sinusoidal AC signal of small amplitude, 10 mV, after an immersion period of 30 min in the corrosive media. The double layer capacitance (Cdl) and charge transfer resistance (Rct) were obtained from the impedance plots as described elsewhere11. Because Rct is inversely proportional to corrosion current density, it was used to determine the inhibition efficiency (IE%) using the relationship; OXYSTELMA ESCULENTUM Stem Extracts as Corrosion Inhibitor for Mild Steel in Acid Medium
  • 2. International Journal of Modern Engineering Research (IJMER) www.ijmer.com Vol. 3, Issue. 4, Jul - Aug. 2013 pp-2456-2459 ISSN: 2249-6645 www.ijmer.com 2457 | Page Where Rct and R0 ct are the charge transfer resistance values in the inhibited and uninhibited solutions respectively. 2.5. Polarization measurements The potentiodynamic polarization curves were recorded using the same cell setup employed for the impedance measurements. The potentials were swept at the rate of 1.66mV/s, primarily from a more negative potential than Eocp to a more positive potential than Eocp through Ecorr. The inhibition efficiencies were calculated using the relationship 12; Where I0 corr and Icorr are the corrosion current densities in the absence and in the presence of inhibitor, respectively III. RESULTS AND DISCUSSION 3.1 Analysis of results of mass loss method The corrosion rates and inhibition efficiency values, calculated using weight loss data, for various concentrations of oxystelma esculentum extract in the presence and absence of KI the corrosion of carbon steel in 0.5M H2SO4 solution are presented in Table.1. It is apparent that the inhibition efficiency increased with the increase in inhibitor concentration in the presence and absence of KI . This behavior can be explained based on the strong interaction of the inhibitor molecule with the metal surface resulting in adsorption. The extent of adsorption increases with the increase in concentration of the inhibitor leading to increased inhibition efficiency. The maximum inhibition efficiency was observed at an inhibitor concentration of 100 ppm. Generally, inhibitor molecules suppress the metal dissolution by forming a protective film adsorbed to the metal surface and separating it from the corrosion medium. The corrosion suppressing ability of the inhibitor molecule originates from the tendency to form either strong or weak chemical bonds with Fe atoms using the lone pair of electrons present on the O and  electrons in benzene ring. It is also seen from table.1 that the leaf extract of oxystelma esculentum at 25 ppm and 100 ppm concentrations shows 55.55 % and 66.00 % inhibition efficiencies respectively, Then the values increased to 80.14 % after adding 25 ppm of KI solution in 0.5M H2SO4 solutions containing 100 ppm of plant extract respectively. This showed a good synergistic effect between oxystelma esculentum extract and KI. Table1.Corrosion rate (CR) of mild steels in 0.5M H2SO4 solutions the absence and presence of inhibitor and the inhibition efficiency (IE) obtained by weight loss method. . Inhibitor concentration (ppm) KI (0) ppm CR (mg cm-2 h-1 ) IE % 0 136.00 - 10 65.42 51.90 25 58.26 57.16 50 46.06 66.13 75 41.26 69.66 100 37.75 72.24 3.2 INFLUENCE OF KI ON THE INHIBITION EFFICIENCY OF STEM EXTRACTS Inhibitor concentration (100ppm) KI (25) ppm CR (mg cm-2 h-1 ) IE % 100 24.26 82.16 3.3 Electrochemical impedance spectroscopic measurements (EIS) Impedance spectra obtained for corrosion of mild steel in 0.5 M H2SO4 contains a semicircle, representing the interaction of metal surface with the corrosive environment.. The -R(CR) model best describes this situation. The semicircle in the impedance plots contain depressed semicircles with the centre below the real axis. The size of the semicircle increases with the inhibitor concentration, indicating the charge transfer process as the main controlling factor of the corrosion of mild steel. It is apparent from the plots that the impedance of the inhibited solution has increased with the increase in the in which
  • 3. International Journal of Modern Engineering Research (IJMER) www.ijmer.com Vol. 3, Issue. 4, Jul - Aug. 2013 pp-2456-2459 ISSN: 2249-6645 www.ijmer.com 2458 | Page the second one represents the interaction of metal surface with the corrosive environment. The first semicircle represents the nature of the corrosive media .Since the conductivity of the corrosive medium is very low, this also behaves like a leaky capacitor. The CR-CR model best describes this situation. The second semicircle in the impedance plots contain depressed semicircles with the centre below the real axis. The size of the semicircle increases with the inhibitor concentration, indicating the charge transfer process as the main controlling factor of the corrosion of mild steel. It is apparent from the plots that the impedance of the inhibited solution has increased with the increase in the concentration of the inhibitor. The experimental results of EIS measurements for the corrosion of mild steel in 0.5 M H2SO4 in the absence and presence of inhibitor are given in Table 3. Said that sum of charge transfer resistance (Rct) and adsorption resistance (Rad) is equivalent to polarization resistance (Rp). Table 3. Impedance parameters obtained from electrochemical impedance studies. Inhibitor concentration ppm Rct Ohm cm2 Cdl µF IE% 0 17.2 9.2578×10-6 - 100 63.00 2.5275×10-6 73.00 100+ 25ppmKI 104 1.5311×10-6 83.50 3.4 Potentiodynamic Polarization studies : Fig 2. Potentiodynamic polarization curves of mild steel immersed in 0.5M H2SO4 solution in the absence and presence of inhibitors
  • 4. International Journal of Modern Engineering Research (IJMER) www.ijmer.com Vol. 3, Issue. 4, Jul - Aug. 2013 pp-2456-2459 ISSN: 2249-6645 www.ijmer.com 2459 | Page Table 4. Corrosion parameters in the presence and absence of inhibitor obtained from polarization measurements. Inhibitor concentration ppm -Ecorr (mV) βc (mV/) βa (mV) Icorr×10*6 µA IE% 0 447 127 68 1.35 100 450 173 72 0.378 72.0 100+25ppmKI 453 195 94 0.278 82.4 The polarization curves obtained for the corrosion of mild steel in the inhibited (100 ppm) and uninhibited 0.5 M H2SO4 solutions in the absence and presence of KI are shown in Fig.2. Electrochemical parameters such as corrosion potential (Ecorr), corrosion current density (Icorr), cathodic and anodic tafel slopes (βc and βa ) and percentage inhibition efficiency according to polarization studies are listed in table 4. Here Icorr decreased with increasing inhibitor concentration. From the figures, it can be interpreted that the addition of this inhibitor to corrosive media changes the anodic and cathodic tafel slopes. The changes in slopes showed the influence of the inhibitor both in the cathodic and anodic reactions. However, the influence is more pronounced in the cathodic polarization plots compared to that in the anodic polarization plots. Even though βc and βa values (table.3) change with an increase in inhibitor concentrations, a high βc value indicates that the cathodic reaction is retarded to a higher extent than the anodic reaction13 . From Fig.2 it is also clear that the addition of the inhibitor shifts the cathodic curves to a greater extent toward the lower current density when compared to the anodic curves. The Ecorr value is also shifted to the more negative side with an increase in the inhibitor concentration. These shifts can be attributed to the decrease in the rate of the hydrogen evolution reaction on the mild steel surface caused by the adsorption of the inhibitor molecule to the metal surface14 . It has been reported that a compound can be classified as an anodic and cathodic type inhibitor on the basis of shift of Ecorr value. If displacement of Ecorr value is greater than 85 mv, towards anode or cathode with reference to the blank, then an inhibitor is categorized as either anodic or cathodic type inhibitor otherwise inhibitor is treated as mixed type15,16 . In our study, maximum displacement in Ecorr value was around 6 mV, indicating the inhibitor is a mixed type and more anodic nature and does not alter the reaction mechanism. The inhibition effect has occurred due to simple blocking of the active sites, thereby reducing available surface area of the corroding metal17,18 . The increase in inhibitor efficiency of inhibited (10mL) 0.5M H2SO4 solution for the corrosion of mild steel after adding 25 ppm KI shows synergism between inhibitor molecules and KI. IV. CONCLUSIONS Results obtained from both electrochemical methods showed that the oxystelma esculentum stem acts as an inhibitor for corrosion of steel in 0.5 M H2SO4 media. Corrosion inhibition action of oxystelma esculentum stem increased as its concentration increases. Inhibition of steel in 0.5 M H2SO4 solution by oxystelma esculentum stem is attributed to adsorption of the phytochemical compounds in this extract. ACKNOWLEDGEMENTS The authors generously acknowledge the support by Dr.R.Somasundaram M.D Dr. R. Arul M.Sc., Ph.D., Dr.S.Vedanayaki M.Sc.,Ph.D.,President ,Principal and head of the department chemistry respectively of kandaswami Kandar’s college,P.Velur for providing necessary chemical and lab facilities to carry out chemical studies References [1] H. Ashassi-Sorkhabi, M. R. Majidi and K. Seyyedi, Applied Surface Science,225(2004)176 [2] A.Y. El-Etre, Corrosion Science,45(2003)2485 [3] A.Y. El-Etre, Corrosion Science,40 (1998)1845 [4] H. Ashassi-Sorkhabi, Z. Ghasemi and D. Seifzadeh, Applied Surface Science,249 (2005)408 [5] M. Bethencourt, F.J. Botana, J.J. Calvino and M. Marcos,Corrosion Science,40(1998)1803 [6] S. Virtanen, M.B. Ives, G.I. Sproule, P. Schmuki and M.J. Graham, Corrosion Science,39(1997)1897. [7] B. Davó and J.J. de Damborenea, Electrochimica Acta,49(2004)4957 [8] A. Aballe, M. Bethencourt, F. J. Botana and M. Marcos, Journal of Alloys and Compounds, 323-324(2001)855 [9] K. C. Emregül and M. Hayvalı, Materials Chemistry and Physics,83(2004)209 [10] S. A. Abd El-Maksoud, Electrochimica Acta,49(2004) 4205 [11] Ashassi-Sorkhabi.H,.Shaabani.B,Seifzadeh.D, Electrochim. Acta,2005 ,50 ,3446. [12] Shahin.M, Bilgie.S, Yilmaz.H, Appl. Surf. Sci.2003,195, 1 [13] Silverman D. C., "Practical Corrosion Prediction Using Electrochemical Techniques", ch. 68 in Uhlig's Corrosion Handbook, 2nd edition (Revie,.R.W, ed.), The Electrochemical Society, 2000. [14] Prabhu., T.V. Venkatesha, A.V. Shanbhag. Praveen. B.M, Kulkarni. G.M,.Kalkhambkar R.G, Mater. Chem. Phys. 2008,108 , 283 [15] Sanghvi. R.A, M.J., et al., Bull. Electrochem.1999, 13, 358. [16] Felicia Rajammal Selvarani, S.Santhanalakshmi, J. Wilson sahayaraja, A. John Amalraj,and Susai Rajendran , Bull. Electrochemistry.2004, 20 , 561-565. [17] Susai RajendranS. Mary Reenkala, Noreen Anthony and Ramaraj,R. Corros Sci,2002, 44, 2243-2252. [18] Scully. J. R., "Polarization Resistance Method for Determination of Instantaneous Corrosion Rates", Corrosion, Vol.2000,56, p. 199.