Lab. of Energy Conversion & Storage...
Transcript of Lab. of Energy Conversion & Storage...
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대기대기대기대기대기대기대기대기 환경에환경에환경에환경에환경에환경에환경에환경에 의한의한의한의한의한의한의한의한 금속금속금속금속금속금속금속금속 소재소재소재소재소재소재소재소재 (organic film coated steel)(organic film coated steel)(organic film coated steel)(organic film coated steel)(organic film coated steel)(organic film coated steel)(organic film coated steel)(organic film coated steel)의의의의의의의의
퇴화퇴화퇴화퇴화퇴화퇴화퇴화퇴화 현상현상현상현상현상현상현상현상 평가평가평가평가평가평가평가평가 연구연구연구연구연구연구연구연구
CorrosionCorrosion
Lab. of Energy Conversion & Storage MaterialsLab. of Energy Conversion & Storage Materials
Produced by K. B. KimProduced by K. B. KimProduced by K. B. KimProduced by K. B. Kim
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• Introduction
• AC Impedance Spectroscopy
• Application of AC Impedance to Corrosion of Organic Film
Coated Steel
• Experimental
• Results and Discussion
• Conclusions
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Organic Coated Metal
Protection of active metals by covering their surface with organic coating
• Mechanical properties of metals
• Preventing metals from corrosion
• Introduction of functional surface properties
Organic Coated Steel
• Steel covered with metallic coatings of Zn and Zn alloys
• Inorganic conversion layer deposited on top of the metallic coating to generate
corrosion resistant interface and to provide link to the organic primer
• Cathodic overcoat as a corrosion resistant organic primer
• Topcoat to give appearance and a barrier between corrosion medium and inner
layers
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Degradation of Organic Coated Metal
Coating degradation
• Penetration of water molecules, ions and oxygen to the polymer/metal interface
• Diffusion of these species through small pores or pathways within the polymer that
facilitates this transport
Corrosion of metal underneath the coating
• Corrosion environment formed at the polymer/metal interface
• Corrosion along the polymer/metal interface : electrochemical reaction
• Blister formation due to corrosion underneath the coating
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Motivation
• Early detection and quantification of coating degradation
• Early detection and quantification of corrosion
• Estimation of corrosion during the initial stage of corrosion when it
may not be visible
• Prediction of useful life of the coating
• Prediction of useful life of the coated metal
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AC Impedance Spectroscopy
(Electrochemical Impedance Spectroscopy, EIS)
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AC Impedance Spectroscopy
E = I Z, Z = Z‘ - jZ“
Z : impedance,
Z‘, Z“ : real part and imaginary part of impedance
~~~~ ~~~~
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AC Impedance Spectroscopy-circuit element
Electrochemical system :
equivalent to electrical circuit composed of parallel or series combination
of R,L, and C
Black BoxAC excitation
Electrochemical system
under test
AC response
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Electrical equivalent circuits
• Uncoated metal under corrosionUncoated metal under corrosionUncoated metal under corrosionUncoated metal under corrosion• Organic film coated metal withOrganic film coated metal withOrganic film coated metal withOrganic film coated metal with
sound coating qualitysound coating qualitysound coating qualitysound coating quality
• Organic film coated metal withOrganic film coated metal withOrganic film coated metal withOrganic film coated metal withunder corrosionunder corrosionunder corrosionunder corrosion
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Electrical equivalent circuits
Xc=1/ (2πf C)At low frequency : infinite capacitive reactance
At high frequency : infinitesimally small capacitive reactance
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Electrical equivalent circuits
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Electrical equivalent circuits
Evaluation of electrical parameters
• Graphical analysis
• Circuit analysis using simulation
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AC Impedance Spectroscopy
5. It is possible to study the influence of
gaseous phases on the corrosion rate under
thin electrolyte
5. It is difficult to study the influence of
gaseous phases on the corrosion rate under
thin electrolyte layers
4. It is possible to determine the corrosion rate
under thin electrolyte layers
4. It is difficult to determine the corrosion rate
under thin electrolyte layers
3. It is easy to determine the mass loss
without removing the sample
3. It is difficult to determine the mass loss
without removing the sample and weighing to
determine the mass change
2. The minimum time required for
determination the mass changes is in the
order of hours
2. The minimum time required for
determination the mass changes more than
one week
1. The corrosion rate can be determined
through a short time exposure
1. The corrosion rate cannot be determined
through a short time exposure
AC Impedance MethodGravimetric and salt spray method
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Application of AC Impedance to Corrosion of
Organic Film Coated Steel
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Degradation of Organic Coated Metal
Coating degradation
• Penetration of water molecules, ions and oxygen to the polymer/metal interface
• Fast diffusion of these species through pathways within the polymer and local
defects formed during production or during the lifetime of the coated materials
Corrosion of metal underneath the coating
• Corrosion environment formed at the polymer/metal interface
• Corrosion along the polymer/metal interface : electrochemical reaction
• Blister formation due to corrosion underneath the coating
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Water Uptake and Corrosion
No electrolytic solution within the metal/organic coating interface,
� neither electrochemical double layer formation nor faradaic reaction occurs.
Once corrosion reactants reach the metallic substrate, corrosion process may start.
Rate of permeation of corrosion reactants (water, ions, oxygen) through the polymer
to the metal surface depends on
� Thickness of the coating
� Diffusivity and solubility within the homogeneous polymer :
chemical nature of the polymeric layer, effective cross linking during curing
� Presence of macro/micro defects in the coating formed during production and life time :
significantly increase the apparent diffusion coefficient of water
� Temperature effect : thermal cycling
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AC Impedance Spectroscopy
• High ohmic resistance of organic coatings :
� impedes the use of DC type electrochemical measurements
• Electrochemical Impedance Spectroscopy (EIS) :
- dielectric properties of film
- processes of coating degradation
- corrosion underneath the coating
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Electrical equivalent circuits
• Organic film coated metal with
sound coating quality before
corrosion reactants reach the
metallic substrate
• Organic film coated metal with
under corrosion after corrosion
reactants reach the metallic substrate
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Electrical equivalent circuit
Ionic resistance of the coating : inversely proportional to average cross section of the
conductive pathway within the coating layer
• Higher than 107 ohmcm2 : high anti corrosion resistance
• 5*105 to 106 ohmcm2 : area of corrosion increased to 0.3 to 1 %
• Lower than 103 ohm cm2 : no protection due to weathered coating
Impedance of metal-organic coating system
• Solution resistance : Rs
• Capacitance of coating : Cc
• Resistance of coating : Rpo
• Charge transfer resistance of metal substrate : Rct
• Double layer capacitance of polymer/ metal interface : Cdl
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Water uptake : Fick’s 2nd law
Finite diffusion of water into organic film
Governing equation
Initial condition
Boundary conditions
Solution
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Water uptake : Water sorption test
Integration of water concentration over organic film thickness
� amount of water uptake
Mt / M∞ = 4 (D½/δπ½) t½
Mt : amount of absorbed water at time t
M∞ : amount of absorbed water at equilibrium
δ : thickness coating
Plot of Mt / M∞ against t½/δ
Diffusion coefficient of water (D)
� calculated from the initial slope of the linear region
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Water uptake : Water sorption test
Z. Z. Lazarevic, Corrosion Science 47 (2005) 823-834
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Water uptake : EIS
Cc = εεoA/l
ε :G Dielectric constant of organic film (4-5 for organic coatings)
εo: Electric permittivity of free space (8.854 * 10-12 F/m)
A : true surface area of electrode
l : thickness of coating
Volume of water fraction = log (Ct/Co) /logG εw
εw : dielectric constant of water (80)
Ct, Co : coating capacitance at time t = t and t = 0
(log Ct - log Co)/ (log C∞ - log Co) = 4 (D½/δπ½) t½
C∞ : coating capacitance at saturation
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Water uptake : EIS, Coating resistance and capacitance
Pore resistance decrease and coating capacitance increase for the first few days
• Pore resistance : presence of ions in water solvent
• Coating capacitance : presence of water in organic film
Time course of pore resistance and coating capacitance, 3% NaCl, Aluminum
Z. Z. Lazarevic, Corrosion Science 47 (2005) 823-834
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Z. Z. Lazarevic, Corrosion Science 47 (2005) 823-834
Water uptake : EIS, Coating resistance and capacitance
Time required to saturate the coating with pure water (6hrs)
� much shorter than that for the initial decrease in pore
resistance.
� close to the time for charge transfer resistance decrease
and double layer capacitance increase
Diffusion coefficient of Cl- ions across polymer
� one order of magnitude smaller than diffusion coefficient
of water (faster mobility and smaller size, molecular radius
1.38A) hydrated ions
1) Diffusion of water into the micropores of the polymer
network, coating saturation with water
2) Development of the conductive macropores through the
coating due to diffusion of Cl-, Na+ and oxygen; slower
moving ions through macropores
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Time course of Rs, Cc, Rpo, Rct and Cdl
With coating degradation and corrosion progress
• Solution resistance : Rs , assumed to be constant
• Capacitance of coating : Cc
• Resistance of coating : Rpo
• Charge transfer resistance of metal substrate : Rct
• Double layer capacitance of polymer/ metal interface : Cdl
Correlation among changes in Rs, Cc, Rpo, Rct and Cdl
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Degradation and Corrosion of Organic Film Coated Steels
S. Gonzalez et al, Progress in Organic Coating, 46 (2003) 317
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Degradation and Corrosion of Organic Film Coated Metal
Lacquer coated Cu in 0.5 M NaCl
K.-M. Yin et al, Surface and Coatings Technology, 106 (1998) 167
Initial resistance of coating Rpo for the 2nd day :
� in the order of 107 ohm
Rapid drop of resistance after 6 days
No significant further change in resistance for a
period of 16-20 days
At 26th day, adhesion of lacquer totally lost
Resistance plateau at low frequencies
� charge transfer resistance of metal surface
plus solution resistance
2nd plateau in high frequencies
�solution resistance
Constant coating capacitance till 20th day
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Degradation and Corrosion of Organic Film Coated Metal
Rpo decrease due to the continuous diffusion of ionic
species within the free volume of coating
Rct decrease with more ions reaching the metal/film
interface, causing corrosion rxn
Reduction in variation of Rpo and Rct during a period of
16-20 days
After the day 22, rapid further drop in Rpo and Rct
Water saturation in 8 days (from Cc)
Cdl plateau in 15 days
Cdl increase at a slower rate than Cc
Water first saturates the coating and then ionic species
follow the flaws in the coating and gradually saturate
the metal surface
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Degradation and Corrosion of Organic Film Coated Metal
Gradual decrease in impedance in 40 days
Impedance and phase angle do not vary in the
period of 40 to 50 days.
Degradation of the film intensifies and a total
delamination of the coating occurs in 70 days.
Bode plot reveals different trends before and
after the interval of 40-50 days.
Coating breaks down in 70 days.
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Degradation and Corrosion of Organic Film Coated Metal
The first semi circle in the high frequency region does not
change much in size
� water borne polymer film remains in a stable structure
The second semi circle that corresponds to the metal
surface impedance shrinks very rapidly
� electrolyte ions quickly saturate the interface during this
period of time.
Rapid decline in charge transfer resistance at the copper
surface during a period of 54 to 64 days
impedance of the polymer film declines very rapidly and
finally disappears
� no protection capability after 50 days
Small semi circle in the low frequencies representative of
the electrode charge transfer resistance does not vary in
size
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Degradation and Corrosion of Organic Film Coated Metal
Coating resistance drops rapidly in less than 10 days
Concurrent Increase in coating capacitance
� Water saturation
In 0 – 40 days, coating resistance and charge transfer
resistance decrease gradually
�Slow diffusion of ionic species within the film
Rapid drop in charge transfer resistance and double layer
capacitance around 40th day
� Breakthrough of the ionic species to the metal surface
After 40 days, charge transfer resistance is close to that
of a piece of uncoated metal
After 60 days, entire coating delamination
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Degradation of Organic Film Coated Metal
Schematic of thermal cycle protocol
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Degradation of Organic Film Coated Metal
Impedance modulus (absolute impedance) during thermal cycling :
reversible behavior
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Degradation of Organic Film Coated Metal
Impedance modulus (absolute impedance) during thermal cycling :
irreversible behavior
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Corrosion of Organic Film Coated Metal
- Anodic blister
- Cathodic blister : no corrosion products
Strong alkaline electrolyte formed during
oxygen reduction,
� stabilization of the oxide on the metal.
Anodic metal dissolution within this zone
� never observed
Delamination of the organic coating
� caused by bond breaking within the adjacent
organic layer through oxidative destruction
of the interface
Instability of the substrate/polymer interface
� linked to the rate of oxygen reduction.