Corrsion Assessment
Corrsion Assessment
Corrsion Assessment
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The Passive Layer
pH >11.5
By alkali,hydroxide concentration
Corrosion rate - 0.1 µm per year
Without the layer ,corrosion - 1,000 times higher -(ACI222
2001)
Excess of chloride ions (Cl−/OH- >0.6) destroys passive
layer
CO2 reacts with alkanity and reduces the pH
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Water molecules attracted
and orient at the metal
surface`
Ions of opposite charge
accumulate near surface`
Cations have more tendency
to hydrate`
Unhydrated anions move
more close to the metal
Anions cause more corrorsive
damage `
Rate depends upon Potential
difference across interface
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Corrosion
Potential
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Half Cell
Potential
Locate corroding rebars
Identify the position for further destructive analysis (cores for
chloride analysis, inspection windows to visually examine the
corrosion state of the rebars etc.)
Evaluate the efficiency and durability of repair work
Design an anode layout of cathodic protection systems or
electrochemical restoration techniques
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Half Cell Potential Apparatus
Voltmeter
Reference Electrode
Connector to reinforcing steel
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Voltmeter
Reference electrode is connected
to the negative terminal
Maximum current of 10 pA
Anodic Site
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Reference Necessary to define type of electrode used
Electrode Defined, constant and reproducible potential versus
the standard hydrogen electrode (SHE) should be
mentioned-
1. Copper / copper sulfate sat CSE + 0.318 V SHE
2. Calomel (Hg / Hg2Cl2) KCl sat. SCE + 0.241 V
SHE
3. Silver chloride (Ag / AgCl) KCl sat. SSCE +
0.199 V SHE
1st one mainly used for site conditions – robust and
fairly accurate
If concrete contaminated with sulphates –other
electrodes used
Porous plug- wet sponge used as conductive bridge
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Electrical connection to the rebars requires a
metallic, electrically sound contact
Contact to the If steel accessible crocodile clips may be used
reinforcement Rust to be cleaned
If embedded in concrete – 25mm drill through
cover zone
4mm drill through rebar & insert a self tapping
screw with attached lead
External metallic feature of the structure such as a
pipe or parapet- provided electrical continuity is
maintained
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Reinforcement continuity may not be present overall or
locally.
Structures such as large structures like bridge decks,
different construction intervals or on very old
structures
Prior continuity check important
The resistance determined with AC measurements
between remote points on a structure should be < 1
Ohm
If the resistance values are higher, multiple electrical
contacts shall be made to the reinforcement
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Structure to be saturated enough to decrease the
electrical resistance of the circuit.
Pre-wetting Continuous electrical circuit formation
Half cell stably placed on the concrete surface for 5
mins to check fluctuation in reading
If voltage reading is stable (+/-0.02 V ) pre-wetting not
required
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Potential Point Point Measurement-
measurement • Testing on points in grids marked on surface
• Spacing depends on the structure
• ASTM C 876 recommends a spacing of 1.2 meter for bridges
• If difference in voltage between adjacent points exceed 150
mV, a closer spacing is suggested
• Higher stability while recording required
• A point representative of larger area
• Lower accuracy
• Measuring underside - reference electrode is filled
withsufficient electrolyte solution.
• Cheap
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Contour Mapping – use of wheels
Potential Mapping 100 m² per hour
Multiple wheel arrangement available
Softwares for easy acquisitions and mapping plot
available with instrument
Also the distance covered as per software checked
frequently with the coordinate system on the structure.
Continuous saturation of contact required
.
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Phase of Corrosion Activity Potential as measured by- CSE
Source: Appendix of ASTM C 876
Phase Potential as measured by Corrosion Activity
Copper Half Cell
results positively
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Situation Half-cell Corrosion of Applicable to
potential shift steel reinforcement ASTM C876
Carbonation/ to negative increase yes
Factors decrease in pH
Increase in chloride to negative increase yes
influencing concentration
Potential results Anodic corrosion
inhibitor
to positive decrease yes
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Carbonation –
The depth of carbonation by spraying phenolphthalein solution was
approximately 9 mm.
The thickness of concrete cover at the web reinforcement was 40
mm.
Carbonation had almost no relationship with corrosion
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• Silver/silver chloride electrode
30 minutes of pre-wetting
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T
• The half-cell potential in summer was shifted by
approximately 40 mV to more negative values than in
winter
• The difference of the gradient became clear in summer
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Average difference was approximately 70 mV on
the whole of the beam
Conversion equation of half-cell potential However, potential gradient almost equal
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Pre- wetting
30min
90min
150min
The gradient is same
Average values in descending order
-- 90min >150min >30min
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As per ASTM C879-- All values
above –350 mV (limit for 90%
probability)
Corrosion risk is low
Hence , numerical criteria do not necessarily agree with the corrosion state
Equipotential contour map is a better tool for assessing the corrosion risk
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In addition to half-cell potential measurements it is often
necessary to use other data such as chloride contents, depth of
carbonation, delamination survey, rate of corrosion results,
environmental exposure conditions,etc.
Consultation with experienced personnel in field of corrosion is
always advisable
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References
E. Nakamura, “Half Cell Potential Measurement to Assess Corrosion Risk of
Reinforcement Steel in a PC Bridge”, International RILEM Conference, 2008.
B. Elsener, “Half-cell potential measurements – Potential mapping on
reinforced concrete structures”, RILEM TC 154-EMC, 2003.
Ping Gu and J.J. Beaudoin, “Obtaining Effective Half-Cell Potential
Measurements in Reinforced Concrete Structures”, 1998.
V.M. Malhotra and N.J. Carino, “Handbook on Non Destructive Testing of
Concrete” ,2nd edition .
Mehta & Monteiro “Concrete : Microstructure, Properties And Materials 4th
Edition”, 4th edition.
ASTM C876 “Standard Test Method for Half-Cell Potentials of Uncoated
Reinforcing Steel in Concrete”,1991 (Reapproved 1999).
Thank You ..
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