The Passivation Behavior of Carbon Steel Rods of Nepal in Different Media

Similar documents
The Electrochemical Behavior of Carbon Steel Wires of Nepal in Different Environments

Roles of Alloying Elements on the Corrosion Behavior of Amorphous W Zr (15 33)Cr Alloys in 1 M NaOH Solution

The Corrosion Behavior of Sputter deposited Ternary Zr (12 18)Cr W Alloys in 12 M HCl Solution

SCC Initiation for X80 Pipeline Steel Under AC Application in High ph Solution

Corrosion Rate Measurement on C-Steel

Some Corrosion Characteristics of Aged Aluminum Alloy 6061 in Neutral and Alkaline Solutions

The Effect of Calcium Nitrite on the Electrochemical Characterization of 3003 Aluminum Alloys in Sea Water. H.Mogawer and R.Brown

THE RELATIONSHIP BETWEEN SURFACE TREATMENTS AND CORROSION RESISTANCE OF HOT-DIP GALVANIZED STEEL. Amirreza Bakhtiari

A Study of Performance of Aluminium Anode by Addition of Zinc in Sea Water

Corrosion of mild steel and 316L austenitic stainless steel with different surface roughness in sodium chloride saline solutions

Galvanic Corrosion Between AISI304 Stainless Steel and Carbon Steel in Chloride Contaminated Mortars

The Evaluation of Corrosion Behavior of AISI 347 Stainless Steel to ASTM A335 Low Alloy Steel Dissimilar Welds

Jagadeesh Bhattarai * Central Department of Chemistry, Tribhuvan Univ., GPO Box 2040, Kathmandu, Nepal.

Passivation Behavior of Iron in Concentrated LiBr Solutions Containing Molybdate and Nitrate at Elevated Temperature

Corrosion Behavior of Cu Zr Ti Nb Bulk Glassy Alloys

Pitting Corrosion of Some Stainless Steel Alloys Preoxidized at Different Conditions

Electrochemical study on magnesium anodes in NaCl and CaSO 4 Mg(OH) 2 aqueous solutions

ONLINE MONITORING OF CORROSION UNDER CATHODIC PROTECTION CONDITIONS UTILIZING COUPLED MULTIELECTRODE SENSORS

Effect of Brij35 on mild steel corrosion in acidic medium

Improvement of corrosion resistance of HVOF thermal sprayed coatings by gas shroud

Corrosion and Passivation Behaviour of Three Stainless Steels in Differents Chloride Concentrations

Galvanic corrosion evaluation of 6061 aluminum coupled to CVD coated stainless steel Elizabeth Sikora and Barbara Shaw 6/9/2016

STATE OF ILLINOIS WILLIAM G. STRATTON, Governor

STAINLESS STEEL SELECTION FOR FLUE GAS DESULFURIZATION EQUIPMENT

ACCELERATED CORROSION TESTING OF GALVANIC COUPLES. James F. Dante, Josh Averett, Fritz Friedersdorf, and Christy Vestal

International Journal of Advancements in Research & Technology, Volume 3, Issue 7, July-2014 ISSN

Effect of Oxidizer on the Galvanic Behavior of Cu/Ta Coupling during Chemical Mechanical Polishing

Corrosion resistance of Au/Ni thin films coated stainless steel used for a PEFC separator

Effect of soil compositions on the electrochemical corrosion behavior of carbon steel in simulated soil solution

Galvanic Corrosion of a Zn/steel Couple in Aqueous NaCl

Corrosion Properties of Enhanced Duplex Steel UNS S32304

The Effect of the ph of Ammonum Nitrate Solution on the Susceptability of Mild Steel to Stress Corrosion Cracking (SCC) and General Corrosion

Analytical investigation of passive films formed on (UNS N-08028) in Simulated Phosphoric acid at different Temperature

CORROSION RESISTANCE OF PLASMA NITRIDED AND NITROCARBURIZED AISI 316L AUSTENITIC STAINLESS STEEL

Threshold Chloride Concentration of Stainless Steels in Simulated Concrete Pore Solution

P-6. Optimization of Citric Acid Passivation for Corrosion Resistance of Stainless Steel 440C. Chi Tat Kwok 1,2 and Wen He Ding 1.

Effects of Surface Finishes on Corrosion Resistance of Welded Stainless Steels

CLEANING AND PREVENTION OF INORGANIC DEPOSITS IN PLATE HEAT EXCHANGERS USING PULSATING CURRENT

Comparative corrosion studies of 2205 duplex steel after electropolishing and passivation in Ringer s solution

Leena Das and Der-Tau Chin Department of Chemical Engineering, Clarkson University Potsdam, New York

CORROSION BEHAVIOR OF TITANIUM METAL IN PRESENCE OF INHIBITED SULFURIC ACID AT 50 o C 1

MMFX 2 (ASTM A 1035, GRADE 100) STEEL REBAR CORROSION PERFORMANCE TESTING IN ACCORDANCE WITH AASHTO MP 18M/MP MMFX Technologies Corporation

Corrosion and inhibition of Cu-Zn alloys in NaCl solution by using permanganate and phosphate anions

Characterization of the Corrosion Scenarios on the Trans-Canada Pipeline (Alberta System)

Short Communication Mechanical Properties and Corrosion Behaviors of Novel Cr2Ni Low-Alloy Construction Steel

Hydrogen Permeation of Pipeline Steel under Sour Condensate Film Condition

Regional Cathodic Protection Design of a Natural Gas Distribution Station

The inhibition of steel corrosion in hydrochloric acid solution by juice of Prunus cerasus

IPC TECHNICAL PAPER SERIES NUMBER 74 LOCALIZED CORROSION OF STAINLESS STEELS IN PAPER MACHINE WHITE WATER DAVID F. BOWERS FEBRUARY, 1979

Erosion corrosion of mild steel in hot caustic. Part II: The evect of acid cleaning

ELECTROCHEMICAL AND SPONTANEOUS PASSIVATION OF THE CoCr ALLOY AS CORROSION PROTECTION

SIGNIFICANCE OF HYDROGEN EVOLUTION IN CATHODIC PROTECTION OF STEEL IN SEAWATER

Laboratory Experiments in Corrosion Engineering II

Electrochemical Impedance Response of Zn and Galvanized Steel Corroding under Marine Atmospheric Environments

ROLES OF PASSIVATION AND GALVANIC EFFECTS IN LOCALIZED CO 2 CORROSION OF MILD STEEL

Potentiodynamic Scanning (PDS) of Stainless Steel Karen Louise de Sousa Pesse

Corrosion Behaviour of 304 Austenitic, 15-5PH and 17-4PH Passive Stainless Steels in acid solutions

Corrosion inhibition of mild steel by ethanolic extracts of Ricinus communis leaves

RAPID MACROCELL TESTS OF 2205 AND XM-28 REINFORCING BARS

Thermodynamics and Electrode Potential ME Dr. Zuhair M. Gasem

Available online at ScienceDirect. Procedia Engineering 86 (2014 )

Effect of Precorrosion and Temperature on the Formation Rate of Iron Carbonate Film

COMPARATIVE CORROSION BEHAVIOR OF PURE COPPER AND BRASS IN 3.5% NaCl SOLUTION

Effect of Heat Treatment on the Corrosion Behaviour of GTM- SU-718 Superalloy in NaCl, HCl and H 2 SO 4 environments

Corrosion is defined in different ways, but the usual interpretation of the term is an attack on a metallic material by reaction with its

Corrosion behavior of Al Si Cu (Sn, Zn) brazing filler metals

Pitting susceptibility of AISI 304 stainless steel after cold rolling Olandir V. Correa a, Mara C.L. de Oliveira b, Renato A. Antunes c.

IMPROVING PITTING CORROSION OF 304 STAINLESS STEEL BY ELECTROPOLISHING TECHNIQUE

IMPROVING PITTING CORROSION OF 304 STAINLESS STEEL BY ELECTROPOLISHING TECHNIQUE

Corrosion Behavior of Twin-Roll Cast Al-Mg and Al-Mg-Si Alloys

DIFFUSION CHARACTERISTICS OF HYDROGEN IN THE TRIP 800 C-Mn-Si-P STEEL. Jaroslav SOJKA, Petr ŠTĚPÁN, Petra VÁŇOVÁ

6340(Print), ISSN (Online) Volume 4, Issue 3, May - June (2013) IAEME AND TECHNOLOGY (IJMET)

Passivity Definitions and Influencing Parameters

Pitting corrosion of type 304 stainless steel and sulfate inhibition effect in chloride containing environments

CHAPTER 2 MATERIALS AND METHODS

Effect of degassing electrolyte on polarisation curve shape with the aim to apply knowledge to electrochemical machining

TRIBOCORROSION EVALUATION OF PROTECTIVE COATING

Initial Stage of Localized Corrosion on Zn - 5 mass% Al Alloy Coated Steels by Pulsed Photon Film Removal Technique

Electrochemical Noise Analysis for Different Green Corrosion Inhibitors for Copper Exposed to Chloride Media

Corrosion characteristics of mild steel in aqueous solution of formic acid containing some acetic acid

STRUCTURE AND ELECTROCHEMICAL BEHAVIOUR OF Fe-9Cr-W ALLOYS WITH VARIABLE CARBON AND TUNGSTEN CONTENT. Jiří RAPOUCH, Jaroslav BYSTRIANSKÝ

MEASURING THE EFFECTIVENESS OF MIGRATING CORROSION INHIBITORS (MCIs) BY ELECTROCHEMICAL TECHNIQUES

Corrosion Behavior of Stainless Steel 304 in Formic Acid Solution

Polarization Functions of Pb-Sn-Cd Alloys Treated with Sulfuric Acid

Inhibition of corrosion of copper by 2,5-dimercapto-1,3,4-thiadiazole in 3.5% NaCl solution

Electrochemical studies of Aluminium 6061 / Titanium Diboride Metal matrix Composites

ONLINE MONITORING OF UNDERCOATING CORROSIONS UTILIZING COUPLED MULTIELECTRODE SENSORS. Xiaodong Sun Corr Instruments, LLC San Antonio TX, USA ABSTRACT

The studies of corrosion resistance of AISI 316Ti SS in Ringer s solution after electropolishing and passivation in nitric acid

Corrosion Behavior of Mild Steel in Seawater from Two Different Sites of Kuala Terengganu Coastal Area

Sealing of Hard Chrome Plating

POLARIZATION MEASUREMENTS ON IRON IN ALKALINE SOLUTIONS AT HIGH PRESSURES AND HIGH TEMPERATURES.

Effect of Alloying Elements on the Corrosion Behavior of Carbon Steel in CO 2 Environments

CORROSION PROTECTION OF MRI230D MAGNESIUM ALLOY BY THE PLASMA ELECTROLYTIC OXIDATION

COMPOSITION, STRUCTURE AND SOME CORROSION PROPERTIES OF AS-RECEIVED NdFeB MAGNETIC MATERIAL AND PROTECTIVE ZnAl COATING

Cast iron deterioration with time in various aqueous salt solutions

834 E. Jafari: J. Mater. Sci. Technol., 2010, 26(9),

ELECTROCHEMICAL CHARACTERISTICS OF ELECTROCHEMICALLY PATINATED BRONZE

2',3-Dicarboxylato-4-Hydroxyazobenzene as Corrosion Inhibitor for Aluminium in Sodium Hydroxide

Effect of Chloride on Localized Corrosion Initiation of Carbon Steel in a CO 2 Aqueous Environment Xin Gao, Bruce Brown, Srdjan Nesic

A Comparison of Cathodic Protection Parameters with High- Strength Pipeline Steels in Soil Solution

Transcription:

The Passivation Behavior of Carbon Steel Rods of Nepal in Different Media J. Bhattarai*, A. Kafle and N. P. Bhattarai Central Department of Chemistry, Tribhuvan University, GPO Box 2040, Kathmandu, Nepal E-mail:bhattarai_05@yahoo.com Abstract The passivation behavior of carbon steel rods of Nepal is studied in 1 M HCl, 0.5 M NaCl and 1 M NaOH solutions at 25 C, open to air using corrosion tests and electrochemical measurements. The corrosion rate of all the examined steel rods is significantly lower in 1 M NaOH solution (about 10-3 mm/y) than those in 0.5 M NaCl (about 10-2 mm/y) and 1 M HCl (about 10 1-10 2 mm/y) solutions. The corrosion rate of SR71 steel rod is remarkably lower (3.65 mm/y) than those of other four different steel rods (3-4 x 10 2 mm/y) of Nepal in 1 M HCl solution. The ennoblement of the open circuit potentials of all the examined steel rod specimens is clearly observed in 1 M NaOH solution than those in 0.5 M NaCl and 1 M HCl solutions. The open circuit potentials of the steel rods are in the passive potential regions of the iron wire in 1 M NaOH solution. Therefore, steel rods of different companies of Nepal showed significantly high corrosion resistance in 1 M NaOH solution at 25 C. Introduction The corrosion of steels is a problem of enormous practical importance because, steels represent the largest single class of alloys in use worldwide. Corrosion of steels is becoming a big problem since the beginning of 20 th century because of the widely use of steels as structural materials. It is believed that only the carbon steel, approximately 85% of the annual steel production of the world, is widely used as engineering material in marine applications, nuclear power and fossil fuel power plants, chemical processing, petroleum production and refining, transportation, pipelines, mining, metal-processing equipment, construction and so on. These are the reasons for the existence of entire industries devoted to provide the corrosion protective systems for steels and irons. The long term durability of new steel structures and the remaining life of existing steel structures is of central interest to their proper maintenance and asset management. This is particularly the case where protective measures of corrosion such as paint coatings, galvanizing or cathodic protection methods are becoming ineffective. To address such corrosion prevention problems, recent research has produced better quality models for the progression of corrosion of steels with time. These employ fundamental characteristics

of steels corrosion as obtained from actual field observations and from laboratory-based electrochemical and other observations. New corrosion problems are arising with the widespread use of different types of steels in various environments up to now. In the 1970s when instruments for surface analysis became available, many corrosion studies had performed by using the surface analysis techniques. 1-8 The electrochemical measurements have been reported to study the corrosion behavior of steels in alkaline solutions 9-11 and in NaCl solutions. 12-16 However, there is no any research works on the corrosion behavior of steels produced or/and used in Nepal. In this context, it is very interesting to study the passivation behavior of various carbon steel rods of Nepal in different environments. The main aim of this research work is to study the passivation behavior of the carbon steel rods produced in Nepal for construction purposes, in acidic 1 M HCl, neutral 0.5 M NaCl and alkaline 1 M NaOH solutions at 25 C, open to air using corrosion tests and electrochemical measurements. Experimental Methods Various carbon steel rods of Nepal, with the average composition (wt %, about: C= 0.17 to 0.25; Si=0.40; Mn= 0.90; S= 0.05; P= 0.05 and the rest iron, were used in this study. The steel rod samples obtained from different companies are named as SR71, SR72, SR73, SR74 and SR75. Prior to the corrosion tests and electrochemical measurement, steel rods having about 7-8 mm diameter of the different steel factories of Nepal were mechanically polished to a mirror finish using edge cutting machine and silicon carbide paper up to grit number 1000 in cyclohexane, degreased with acetone and dried in air. The corrosion rate of the steel rod specimens was estimated from the weight loss after immersion for 190-264 hours in 100 ml of 1 M HCl, 0.5 M NaCl and 1 M NaOH solutions at 25 C, open to air. The open circuit potentials of the steel rod specimens were measured after immersion for 2 hours in 1 M HCl, 0.5 M NaCl and 1 M NaOH solutions at 25 C, open to air. The cathodic and anodic potentiostatic polarization measurements were also carried on a steel wire of Nepal in 1 M NaOH solution at 25 C. A platinum mesh and saturated calomel electrode were used as counter and reference electrodes, respectively. The sample specimens were used as a working electrode. The potential given in this paper is relative to saturated calomel electrode (SCE). Results and Discussion Figures 1(a), 1(b) and 1(c) show the corrosion rates of five carbon steel rods produced by five different steel companies of Nepal, after immersion in 1 M HCl, 0.5 M NaCl and 1 M NaOH solutions, respectively at 25 C, open to air. In 1 M HCl, the corrosion rates

of all the examined steel rods are in the range of about 10 1 mm/y. Among these five different steel rods, sample SR71 of the company one shows the lowest corrosion rate of about 3.65 mm/y which is nearly one order of magnitude lower than those of the corrosion rates of samples of other four different companies ( that is, SR72, SR73, SR74 and SR75). The corrosion rates of the SR73 and SR74 samples are slightly higher than those of the SR72 and SR75 samples in 1 M HCl solution 25 C. This trend of the different corrosion rates of the steel rods of different companies of Nepal is not clearly observed in neutral 0.5 M NaCl and alkaline 1 M NaOH solutions at 25 C. In 0.5 M NaCl, all five different steel rods show the almost same corrosion rates (that is, between 6.1 to 8.6x10-2 mm/y) after immersion for eleven days. The sample SR74 shows slightly higher corrosion rate than others. Similarly, the corrosion rates of all five different steel rods are almost same corrosion rates (that is, 1.6-3.0 x 10-3 mm/y) after immersion for 264 hours in alkaline 1 M NaOH solution at 25 C. These results revealed that the corrosion rate of all examined carbon steel rods in 1 M HCl solution is significantly higher than those in 0.5 M NaCl and 1 M NaOH solutions. All the examined steel rods of different companies of Nepal show very high corrosion resistance in 1 M NaOH solution at 25 C. Electrochemical measurements were carried out for a better understanding of the passivation behavior of the steel rods of Nepal after immersion for 2 hours in acidic 1 M HCl, neutral 0.5 M NaCl and alkaline 1 M NaOH solutions at 25 C, open to air. Figures 2(a) and 2(b) show the changes in open circuit potentials of samples SR71 and SR72, respectively with immersion time for 2 hours in 1 M HCl, 0.5 M NaCl and 1 M NaOH solutions at 25 C. In both steel rod samples, the open circuit potentials in 1 M HCl, 0.5 M NaCl and 1 M NaOH solutions after immersion for about 30 minutes reach a steady state and almost same values of about -460, -580 and -160 mv (SCE), respectively. The nature of changes of the open circuit potentials of the steel rods with immersion time in acidic, neutral and alkaline solutions are not same. The changes in the open circuit potentials for the examined steel rods are not significant with immersion time in 1 M HCl solution. In 0.5 M NaCl solution, the open circuit potentials shifted to more negative (or less noble) direction with immersion time as shown in Figs 2(a) and 2(b). However, the open circuit potentials of the steel samples are sharply shifted to more positive (or more noble) direction with immersion time in alkaline 1 M NaOH solution as shown in Figs 2(a) and 2(b). Consequently, the open circuit potential of the steel rods is more negative value (i.e., about -580 mv, SCE) in 0.5 M NaCl solution than that in 1 M HCl solution. However, in 1 M NaOH, the open circuit corrosion potential is more positive value (i.e., about -160 mv, SCE) than that in 0.5 M NaCl solution. These results revealed that steel rods are more passive in alkaline 1 M NaOH than those in acidic 1 M HCl and neutral 0.5

(a) (b) (c) Figure 1: Corrosion rates of steel rods of different five companies of Nepal in (a) 1 M HCl, (b) 0.5 M NaCl and (c) 1 M NaOH solutions at 25, open to air.

Steel ro d SR 71 o f N epal in different so lutio ns at 25 o C o pen to air 0-100 Steel ro d SR 72 o f N epal in different so lutio ns at 25 o C o pen to air 0-100 -200-300 -400-500 -600-700 0 20 40 60 80 100 120 Immersion time / min. (a) 1M HC l 0.5 M NaC l 1M N aoh -200-300 -400-500 -600-700 0 20 40 60 80 100 120 Immersio n time / min. (b) 1M HC l 0.5 M N ac l 1M N aoh Figure 2: Changes in open circuit potentials for (a) SR71 and (b) SR72 steel rods of Nepal in different environments at 25 C, open to air as a function of immersion time. Figure 3: The potentiostatic polarization curve of the steel wire of Nepal in 1 M NaOH solution at 25 C, open to air. M NaCl solutions. Furthermore, figure 3 shows the potentiostatic polarization curve for a steel wire after polarization for 1 h in alkaline 1 M NaOH solution at 25 C. The steel wire shows clearly the active-passive transition and transpassivation. The steel wire is active at the potential range between -500 to -200 mv (SCE) while it is passive at the

potential range between -150 to 250 mv (SCE) in 1 M NaOH solution. The passive current density is in the range of 10-2 A/m 2 in 1 M NaOH solution. Transpassivity is clearly seen after polarization at 300 mv (SCE) or more anodic potentials probably due to the formation of soluble ferrate (FeO 2-4 ) in 1 M NaOH solution. 17 Consequently, the corrosion rates of steel rods are significantly higher in 1 M HCl than those in 0.5 NaCl and 1 M NaOH solutions as shown in Fig. 1. This is mostly due to an ennoblement of the open circuit potentials of steel rods at passive potential regions (that is, between -150 to 250 mv, SCE) in 1 M NaOH solution at 25 C. Similarly, the open circuit potentials of the steel rods in 1 M HCl (that is, about -460 mv, SCE) are in more active potential regions (that is, -500 to -200 mv, SCE) of the steel wire in alkaline solution at 25 C as shown in Fig. 3. Conclusions The passivation behavior of the carbon steel rods of Nepal used mainly for construction purposes is studied in acidic 1 M HCl, neutral 0.5 M NaCl and alkaline 1 M NaOH solutions at 25 C, open to air by corrosion tests and electrochemical measurements. The following conclusions are drawn: 1. The corrosion rate of the steel rods of Nepal in 1 M HCl is significantly higher than those in 0.5 M NaCl and 1 M NaOH solutions. The corrosion rates of different steel rods of Nepal are not same in acidic solution. However, the corrosion rates of all the examined steel rods are almost in the same range in neutral and alkaline solutions, respectively. 2. The open circuit potentials of the carbon steel rods are located in the passive potential regions of steel wire in alkaline 1 M NaOH solution while the open circuit potentials of steel rods are located in the active regions of the steel wire in neutral 0.5 M NaCl solution. Acknowledgments Authors are thankful to the Head, Central Department of Chemistry, Tribhuvan University, Nepal for providing us the available research facilities to conduct this research work. An appreciation goes to Mr. Lalanath Subedi, Asstt. Dean, Institute of Engineering, Tribhuvan University for providing facilities of the edge cutting machine. References 1. Holliday, J. E. and Frankenthal, R. P., J. Electrochem. Soc., 1972, 119, 1190-1192.

2. Asami, K., Hashimoto, K. and Simodaira, S., Corros. Sci., 1978, 18, 151-160. 3. Zou, J. -Y. and Chin, D. -T., Electrochimica Acta, 1987, 32, 1751-1756. 4. Kamimura, T. and Stratmann, M., Corros. Sci., 2001, 43, 429-447. 5. Olsson, C. -O. A and Landolt, D., Electrochimica Acta, 2003, 48, 1093-1104. 6. Shibata, T., Corros. Sci., 2007, 49, 20-30. 7. Fujimoto, S. and Tsuchiya, H., Corros. Sci., 2007, 49, 195-202. 8. Yang, S. and Macdonald, D. D., Electrochimica Acta, 2007, 52, 1871-1879. 9. Abdul Azim, A. A., Anwar, M. M. and Sanad, S. H., Corros. Sci., 1969, 9, 405-412. 10. Newman, J. E., Corros. Sci., 1981, 21, 487-503. 11. Gonzalez, J. A., Miranda, J. M., Otero, E. and Felius, S., Corros. Sci., 2007, 49, 436-448. 12. Wendt, J. L. and Chin, D. -T.,Corros. Sci., 1985, 25, 889-900. 13. Nishikata, A., Yamashita, Y., Katayama, H., Tsuru, T., Usami, A., Tanabe, K. and Mabuchi, H.,Corros. Sci., 1995, 37, 059-2069. 14. Melchers, R. E. and Asce, M.,J. infrastruct. Syst., 2006, 12, 54-162. 15. Reffass, M., Sabot, R., Savall, C., Jeannin, M., Creus, J. and Refait, Ph., Corros. Sci., 2006, 48, 709-26. 16. Isaacs, H. S., Looi, Y. M. and de Wit, J. H. W.,Corros. Sci., 2007, 49, 53-62. 17. Uhlig, H. H. and Revie, R. W., in Corrosion and Corrosion Control, 3 rd edition, 1991, p.97.