Presentation on theme: "Electrochemical Techniques for Corrosion Measurements"— Presentation transcript:
1Electrochemical Techniques for Corrosion Measurements
2AssignmentPresent a critical examination of the proposed mechanisms of CO2 and H2S corrosion with particular emphasis on the cathodic (oxidation) reactions.Due Date 5 June 2009
3Corrosion Measurements Involve the use of a potentiostat for applying a potential (relative to a reference electrode) and measuring the current (flowing from the working electrode to the counter or auxiliary electrode)*ensure specimen potential (w.r.t. counter) constant … even though solution resistance might alter.3
4The Manual Potentiostat Variable High Voltage Source VAmmeter (current)High Impedance Voltmeter ΩWorking ElectrodeReference ElectrodeAuxiliary Electrode
5Electrochemical Impedance Spectroscopy ResistanceOhms LawFor a resistor, R, it follows Ohm’s Law at all current and voltage levelsThe resistance value is independent of frequencyAC current and voltage signals through a resistor are in phase with each other
6Electrochemical Impedance Spectroscopy Impedance applies to AC voltage and currentLike resistance impedance is a measure of the ability of a circuit to resist the flow of electrical currentThe excitation potential or AC voltage can be expressed as a function of time
7Electrochemical Impedance Spectroscopy The relationship between radial frequency ω (radians s-1) and frequency (f) hertz is:The response to the AC voltage is given by:
8Electrochemical Impedance Spectroscopy Similar to Ohm’s lawThe important point to remember is that when an AC voltage is applied to a pure capacitor the resulting AC current is shifted in phase by 90oThere is no phase shift for a pure resistor
9Electrochemical Impedance Spectroscopy Current phase shift due to impedance. Through a capacitor this phase shift is 90oApplied VoltageResulting Current
10Electrochemical Impedance Spectroscopy Randles circuit for a simple corroding systemRs = the solution resistanceRct = the charger transfer (polarisation resistance)Cdl = the double layer capacitance
11Electrochemical Impedance Spectroscopy Nyquist plot for the Randels circuit← Increasing FrequencyCapacitanceCharge transfer resistance = Rtotal - RsSolution ResistanceResistance
12EIS Nyquist PlotsA Nyquist plot is made up of a series of vectors representing the total magnitude of the resistance and capacitance componentsNon Resistive ComponentPhase angle
15EIS (Summary)We start here at the high frequency
16EIS Diffusion or Mass Transfer controlled process Nyquist plot - Warburg Impedance←Frequency
17EIS Diffusion or Mass Transfer controlled process Bode Impedance plot Frequency →
18EIS Diffusion or Mass Transfer controlled process Bode Phase plot Phase AngleFrequency →
19EIS – Mass Transfer Controlled Process (Summary) NyquistBode ImpedanceBode Phase
20EIS Equivalent Circuit for a Mixed Kinetic and Charge Transfer Controlled Process
21EIS Bode Plots for the Mixed Controlled Reaction ImpedancePhase
22EIS Equivalent Circuit for a Filmed Corroding Surface (E. g EIS Equivalent Circuit for a Filmed Corroding Surface (E.g. Failed Coating)
23EIS for a Filmed Corroding Surface (E.g. Failed Coating) Bode Impedance (MagnitudeNyquistBode Phase Angle
24Linear Polarization Method Valid for corrosion under activation control.Involves applying a small perturbation to the potential around Ecorr (i.e., ± ∆E ≈ 10 mV).N.B. ∆i for summed curve = ia + |∆ic| (∆ia=x)Slope of summed curve (measure E vs i for system) is difference between slopes of curves for the coupled reactions: Sa - Sc
25The curves are ~linear within ~20mV – Sa and Sc are constant The curves are ~linear within ~20mV – Sa and Sc are constant. For ∆E around Ecorr, Sa and Sc are related to icorr (the required quantity): assuming the high-field approximation for the individual reactionsNow:slopeslopeorPolarization Resistance is measured. The Tafel coefficient ba and bc must be known.
26Remember: during linear polarization measurements we plot E vs i (not log i) around the corrosion potential:= polarization resistance26
27Linear PolarizationThis involves the application of low over-potentials and therefore the currents are relatively very small. This means that the charging current (capacitance current) can make a significant contribution to the noise or background current.Use slow scan rates and perform a cyclic scan to check whether you are measuring capacitance.The reverse scan should produce an iE curve that retraces over the forward recorded iE curve.The iE curve can be curved due to a difference in the anodic and cathodic Tafel slopes.
28Linear PolarizationIt is important to view the iE curve. If the iE curve is curved, the polarization resistance can be obtained by drawing a line that is tangential to the curve at Ecorr and at zero current.Some portable instruments use a potential-step method. In this case the current, at, for example, -10 mV and +10 mV is measured and Rp is computed from these measurements.The advantage of this technique is that the current measurements are made at a constant voltage and therefore the charging current is zero.The disadvantage is that no iE curve is recorded and therefore an error can be introduced if there is curvature in the iE graph
29Linear PolarizationThe portable instruments that use the potential-step technique, usually apply a high frequency AC signal before the measurement to determine the solution resistance and subtract this value from the measured polarization resistance.
31Tafel Method We can only measure the net current across the specimen electrode – at the corrosion potential there is no net current (only local anode – cathode currents which constitute the corrosion current). We cannot measure corrosion rate directly, though we need icorr.Measure potential and current at some distance on either side of Ecorr – extrapolate E - log i curves (in same quadrant) back to Ecorr …Plot of the total current (iT = io + ic) versus potential showing the extrapolation of the Tafel regions to the corrosion potential, Ecorr, to yield the corrosion current, icorr.
32PassivationUnder certain conditions of potential and pH, some metals form protective films, i.e., they passivatePourbaix diagram for the iron/water/dissolved oxygen system showing the effect of potential in moving the system from a corrosive (active) region (point 1) to a passive region (point 2)We can exam the kinetics using a potentiodynamic scan and Evans diagram
33The polarization curve for the anodic reaction of a passivating metal drawn for potentials more noble than the equilibrium potential (Ee)aOxidative dissolution of oxide (e.g., Cr2O3 CrO42-)(Ee)M/MO is the equilibrium potential for oxide/hydroxide formation“Flade”Tafel region(icrit is min. reaction rate required to initiate film growth by precipitation of Mn+)The region attained by the metal in a given environment depends upon the cathodic reaction i.e., where the cathodic curve cuts the above anodic curve.33
34Tafel Extrapolation Technique Involves measurements at high over-potential in which logi is recorded.The best method of performing these measurements is by :1) Using two identical electrodes and recording the anodic curve on one electrode and the cathodic curve on the other electrode. In each case starting at the open circuit potential Eoc (or Ecorr)2) Performing the cathodic curve on one electrode starting the scan from Eoc. Turning off the potentiostat and monitoring Eoc until it returns to its original value. The anodic scan is then recorded again starting at the Eoc.
35Tafel Extrapolation Technique Before commencing a Tafel measurement, it is generally best to allow your metal electrode to reach a steady state potential. This can be observed by performing a potential time measurement in which Ecorr is monitored with time.Scan Rates are normally in the range of 0.1 mV to 5.0 mV per second. The cathodic plot is scanned to an over-potential of about 400 mV.Anodic potentials can be scanned much higher depending on what information needs to be obtained.
36Cyclic Pitting ScansThe technique is used to evaluate the susceptibility of metals to pitting corrosion in a particular environment. It is applicable to metals such as stainless steels, high nickel alloys and aluminium, which form a passive protective film.With this technique, the potential is scanned to voltages in the transpassive region.Exceeding the passive region is indicated by a sudden increase in current. At this stage the voltage scan is reversed, usually when the current reaches a certain current density (0.5 mA cm-2)
37Cyclic Pitting ScansThe extent of the hysteresis in the reverse scan is an indication of the susceptibility to pitting corrosion.Pitting corrosion is considered to stop at the potential where the iE curve from the reverse scan crosses the iE curve of the forward scan.The sudden increase in current can be due to three processes:1) Onset of pitting corrosion2) Trans-passive uniform corrosion3) The oxygen evolution reactionIn the case of trans-passive corrosion, the slope of the iE curve is not as steep compared to pitting corrosion and oxygen evolution.In the case of oxygen corrosion, the reverse iE curve normally will retrace over the forward iE curve.
38Harmonic Analysis Butler Volmer Equation When an electrode is polarized near the corrosion potential by a sinusoidal voltage of frequency ω and amplitude U0, then the current density of the Faradaic process is given by:
39Harmonic AnalysisThe current densities of the Faradaic process will have a distorted sinusoidal form due to the non-linear nature of the cathodic and anodic partial processes in a polarization curve.The amplitudes of the harmonic components can be obtained by Fourier series expansion of the exponential terms
40Harmonic AnalysisThe simplified magnitude of the first three harmonic components are given by:
41Harmonic AnalysisThe technique has been verified by the work of Will Durnie, Curtin University.He compared corrosion rates from HA with those obtained using linear polarization measurements and Stern Geary equation.When the Tafel slopes obtained from HA were placed in the Stern Geary equation an excellent correlation was obtained.
42Harmonic AnalysisDurnie, W. H.,Curtin University
43Electrochemical Noise (ECN) ECN measures the current/voltage response between two (largely) identical electrodes.The two electrodes are coupled together (short circuited together) through a zero resistance ammeter (ZRA).The random fluctuations of current is measure by the ZRA.At the same time the random fluctuations in voltage noise at the coupled electrodes is measured with respect to a reference electrode.
45Rotating dual cylinder electrode (RDCE) Standard electrochemical cell with reference, auxiliary and RDCEThe RDCE is useful for performing ECN MeasurementsECN uses identical electrodes. In the example shown the electrode areas are not the same since this RDCE was used to investigate preferential weld corrosion