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CORROSION AND DEGRADATION
OF MATERIALS
By: www.mechXplain.com
Definition
 Conventional engineering materials are not able
to serve at their full potential for long periods of
time i.e. they gets deteriorated during the service.
 They are many reasons for deterioration of
engineering materials, like physical, chemical,
mechanical, weather, etc.
 Chemical deterioration is most common in metals,
and also observed to some extent in ceramics. It
is known as corrosion.
 Physiochemical deterioration of polymers is
known as degradation of polymers.
Why study Corrosion and Degradation
of Materials?
 With a knowledge of the types of and an
understanding of the mechanisms and causes
of corrosion and degradation, it is possible to
take measures to prevent them from occurring.
 For example, we may change the nature of the
environment, select a material that is relatively
nonreactive, and/or protect the material from
appreciable deterioration.
Corrosion of metals
 Corrosion of metals is mainly due to
electrochemical reactions.
 It is also most influenced by temperature and
concentration gradients.
 Relative tendency of a metal to get corroded is
presented in terms of its electro-motive force
(EMF).
 Standard EMF series is suitable for easy
recognition of basic elements for their relative
tendency towards corrosion.
 Another usefulness of the series is to pick material
for cathodic protection.
Corrosion rate
 The corrosion rate, or the rate of material removal as a
consequence of the chemical action, is an important
corrosion parameter. This may be expressed as the
corrosion penetration rate (CPR), or the thickness loss of
material per unit of time. The formula for this calculation is
Where :
W = Weight loss
t = exposure time
(Rho) = Density
A = exposed specimen area
K = constant,(Its magnitude depending on the system of units used.)
Passivity
 Some normally active metals and alloys,Under
particular environmental conditions, lose their
chemical reactivity and become extremely inert. This
phenomenon, termed passivity, is displayed by
chromium, iron , nickel ,titanium and many of their
alloys.
 At relatively low potential values, within the “active”
region the behaviour is linear as it is for normal
metals. With increasing potential, the current density
suddenly decreases to a very low value that remains
independent of potential; this is termed the “passive”
region.
Finally, at even higher potential values, the
current density again increases with potential in
the “transpassive” region.
Forms of metal corrosion
Corrosion of metals is
classified based on the
manner in which it is
manifest into eight forms.
 Uniform corrosion:
As name suggests,
corrosion occurs over
entire exposed surface.
Less of detrimental. Easy
to monitor and control. Is
it also most common
form. Painting is best
counter measure for it.
 Galvanic corrosion:
Occurs when two metal
with different EMF are
electrically connected, of
which one gets corroded.
Counter measures
include: insulation;
pairing metals with less
difference between their
EMF; altering the
corrosive environment;
tailoring the design of
components w.r.t. their
EMF.
 Crevice corrosion: This occurs as a result of
concentration gradient within a component.
Corrosion occurs at the site of lower
concentration. Counter measures include:
welding instead of riveting; removing scales,
etc.
Rivetholes
 Pitting: Other localized corrosion. Difficult
monitor and very dangerous. Material removal
is minimal, but occurs in normal to surfaces.
Counter measures: polishing of surface, and
other common methods.
 Inter-granular corrosion: This is due to
concentration difference at micro-level. Grain
boundaries are inferior to grains, and more
prone to corrosion. Counter measures: suitable
heat treatment; addition of alloying elements;
low %C in steels.
 Selective leaching: Occurs in selective
metals. It is selective removal of a particular
metal from the component. Example –
dezincification of brass. Counter measures:
change of material; cathodic protection.
 Erosion-Corrosion:
 It is acceleration of corrosion due to mechanical
actions. All metals and alloys are prone to this
form of corrosion. More damaging in case of
metals with passive scales.
 Counter measures: change of component
design; clearing the fluid particles.
 Stress concentration: Also known as stress
corrosion cracking (SCC). Result of combined
action of tensile stresses and corrosive
environment. Counter measures: change of
environment; cathodic protection; addition of
inhibitors
Corrosion of ceramics
 As ceramics are made of metals and non-metals,
they can be considered as already corroded.
 Ceramics do get deteriorated during their service
under extreme temperatures and external loads.
 Factors effecting life of ceramic components
include: temperature, external loads, vibrations,
environment, etc.
 Life span of ceramics can be increased by
controlling the environment they are exposed to;
operational loads and temperatures; altering the
component design.
Degradation
 Degradation is a process that will result the
change in properties of materials such as
tensile strength, colour and so on.
 It will reduce the ability of the material to
perform their intended function.
 Actually every natural phenomena will cause
the degradation.
 Such as light, heat, short wave length,
electronegative radiation, electro active
emission, chemicals, stress, bacterial etc.
Types of degradation process
 Thermal: Occurs at elevated temperature
 Mechanical: Application of force
 Ultrasonic: Application of sound
 Hydraulic: Function groups sensitive to water
 Chemical: Occurs when corrosive chemical
or gas comes in contact
 Biological: Attached by micro organism
 Radiation: On exposure of sunlight or high
energy radiation
Forms of degradation
 Swelling and Dissolution:
 solute molecules actually fit into the molecular
structure.
 When exposed to humid environment, polymers
gets swelling due to diffused and absorbed
moisture.
 It may also involve dissolution of polymers, hence
swelling is considered as partial dissolution.
 Dissolution involves complete solution of polymer
in solvent.
 Weathering:
 When exposed to outdoor weather for long
periods of time, polymer may get decolored,
distort from their original shape.
 This may be due to many actions including
radiation of the sun, oxidation, etc.
 Bond rupture:
 This is main form of polymer failure.
 Bond rupture, also known as scission, may
occur due to effects like radiation, heat energy,
or chemical reactions.
 When polymers are exposed to certain types of
radiation, which may result in broken bonds
and rearrangement of atoms leads to
degradation of polymers.
 At elevated temperatures, bonds in polymers
may get weakened, leading to deterioration of
polymers.
 Some chemical elements like oxygen, ozone
can alter the chain scission rate as a result of
chemical reactions.
Does Stainless Steel Corrodes ?
Ferrous oxide doesn’t form a continuous layer on the steel because the oxide molecule
has a larger volume than the underlying iron atoms, and eventually spalls off
leaving fresh steel exposed which then starts a deleterious rusting cycle.
So Al should corrode more ?
 Aluminium corrodes and an Aluminium Oxide
(Al2O3) layer forms which is impervious
(Doesn't allowing fluid to pass through)
Prevent Corrosion
1. Galvanising
This is when the zinc layer stops oxygen/water or salt from
attacking the iron. An advantage is that a scratch will still
slow corrosion (as Zn is higher in the series) via sacrificial
protection.
 Coatings generally protect the metal by imposing a
physical barrier between the metal substrate and the
environment.
 Three common types of coatings are organic, inorganic,
and metallic. Using paint or grease physically stops
oxygen/water/salt from reaching the metal like this
2. Coatings (Painting/ Greasing)
3. Electroplating
This process deposits a thin layer of metal on
the object being protected. Tin plating requires
the object being protected to be the negative
terminal and surrounded by a solution of the
ions of the metal being deposited on to the
object. The negative charge attracts positive
ions.
4. Sacrificial Protection
This method works by taking a metal higher up
the reactivity series is connected to the
iron/steel and donates its electrons to any iron
ions that might have formed, stopping it from
corroding.
5. Alloying:
Corrosion can be also prevented by alloying some
metals with other metals. The resultant metals
called alloys do not corrode easily, e.g. stainless
steel
Austenitic S.S
Max. of 0.15% carbon
Min 16% chromium
Sufficient Ni
 According to them, the relatively pure composition of the iron used, presence
of high amounts of phosphorus (as much as 1 per cent against less than
0.05 per cent in today's iron) and absence of sulphur/magnesium in the iron
are the main reasons for its longevity.
Iron Pillar Of Delhi
Proudly Standing Since
402 CE (1600 years)
Thank You
www.mechXplain.com

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Corrosion of material - Engineering Metallurgy

  • 1. CORROSION AND DEGRADATION OF MATERIALS By: www.mechXplain.com
  • 2.
  • 3. Definition  Conventional engineering materials are not able to serve at their full potential for long periods of time i.e. they gets deteriorated during the service.  They are many reasons for deterioration of engineering materials, like physical, chemical, mechanical, weather, etc.  Chemical deterioration is most common in metals, and also observed to some extent in ceramics. It is known as corrosion.  Physiochemical deterioration of polymers is known as degradation of polymers.
  • 4. Why study Corrosion and Degradation of Materials?  With a knowledge of the types of and an understanding of the mechanisms and causes of corrosion and degradation, it is possible to take measures to prevent them from occurring.  For example, we may change the nature of the environment, select a material that is relatively nonreactive, and/or protect the material from appreciable deterioration.
  • 5. Corrosion of metals  Corrosion of metals is mainly due to electrochemical reactions.  It is also most influenced by temperature and concentration gradients.  Relative tendency of a metal to get corroded is presented in terms of its electro-motive force (EMF).  Standard EMF series is suitable for easy recognition of basic elements for their relative tendency towards corrosion.  Another usefulness of the series is to pick material for cathodic protection.
  • 6. Corrosion rate  The corrosion rate, or the rate of material removal as a consequence of the chemical action, is an important corrosion parameter. This may be expressed as the corrosion penetration rate (CPR), or the thickness loss of material per unit of time. The formula for this calculation is Where : W = Weight loss t = exposure time (Rho) = Density A = exposed specimen area K = constant,(Its magnitude depending on the system of units used.)
  • 7. Passivity  Some normally active metals and alloys,Under particular environmental conditions, lose their chemical reactivity and become extremely inert. This phenomenon, termed passivity, is displayed by chromium, iron , nickel ,titanium and many of their alloys.  At relatively low potential values, within the “active” region the behaviour is linear as it is for normal metals. With increasing potential, the current density suddenly decreases to a very low value that remains independent of potential; this is termed the “passive” region.
  • 8. Finally, at even higher potential values, the current density again increases with potential in the “transpassive” region.
  • 9. Forms of metal corrosion Corrosion of metals is classified based on the manner in which it is manifest into eight forms.  Uniform corrosion: As name suggests, corrosion occurs over entire exposed surface. Less of detrimental. Easy to monitor and control. Is it also most common form. Painting is best counter measure for it.
  • 10.  Galvanic corrosion: Occurs when two metal with different EMF are electrically connected, of which one gets corroded. Counter measures include: insulation; pairing metals with less difference between their EMF; altering the corrosive environment; tailoring the design of components w.r.t. their EMF.
  • 11.
  • 12.  Crevice corrosion: This occurs as a result of concentration gradient within a component. Corrosion occurs at the site of lower concentration. Counter measures include: welding instead of riveting; removing scales, etc. Rivetholes
  • 13.  Pitting: Other localized corrosion. Difficult monitor and very dangerous. Material removal is minimal, but occurs in normal to surfaces. Counter measures: polishing of surface, and other common methods.
  • 14.  Inter-granular corrosion: This is due to concentration difference at micro-level. Grain boundaries are inferior to grains, and more prone to corrosion. Counter measures: suitable heat treatment; addition of alloying elements; low %C in steels.
  • 15.  Selective leaching: Occurs in selective metals. It is selective removal of a particular metal from the component. Example – dezincification of brass. Counter measures: change of material; cathodic protection.
  • 16.  Erosion-Corrosion:  It is acceleration of corrosion due to mechanical actions. All metals and alloys are prone to this form of corrosion. More damaging in case of metals with passive scales.  Counter measures: change of component design; clearing the fluid particles.
  • 17.  Stress concentration: Also known as stress corrosion cracking (SCC). Result of combined action of tensile stresses and corrosive environment. Counter measures: change of environment; cathodic protection; addition of inhibitors
  • 18. Corrosion of ceramics  As ceramics are made of metals and non-metals, they can be considered as already corroded.  Ceramics do get deteriorated during their service under extreme temperatures and external loads.  Factors effecting life of ceramic components include: temperature, external loads, vibrations, environment, etc.  Life span of ceramics can be increased by controlling the environment they are exposed to; operational loads and temperatures; altering the component design.
  • 19. Degradation  Degradation is a process that will result the change in properties of materials such as tensile strength, colour and so on.  It will reduce the ability of the material to perform their intended function.  Actually every natural phenomena will cause the degradation.  Such as light, heat, short wave length, electronegative radiation, electro active emission, chemicals, stress, bacterial etc.
  • 20. Types of degradation process  Thermal: Occurs at elevated temperature  Mechanical: Application of force  Ultrasonic: Application of sound  Hydraulic: Function groups sensitive to water  Chemical: Occurs when corrosive chemical or gas comes in contact  Biological: Attached by micro organism  Radiation: On exposure of sunlight or high energy radiation
  • 21. Forms of degradation  Swelling and Dissolution:  solute molecules actually fit into the molecular structure.  When exposed to humid environment, polymers gets swelling due to diffused and absorbed moisture.  It may also involve dissolution of polymers, hence swelling is considered as partial dissolution.  Dissolution involves complete solution of polymer in solvent.
  • 22.
  • 23.  Weathering:  When exposed to outdoor weather for long periods of time, polymer may get decolored, distort from their original shape.  This may be due to many actions including radiation of the sun, oxidation, etc.
  • 24.  Bond rupture:  This is main form of polymer failure.  Bond rupture, also known as scission, may occur due to effects like radiation, heat energy, or chemical reactions.  When polymers are exposed to certain types of radiation, which may result in broken bonds and rearrangement of atoms leads to degradation of polymers.
  • 25.  At elevated temperatures, bonds in polymers may get weakened, leading to deterioration of polymers.  Some chemical elements like oxygen, ozone can alter the chain scission rate as a result of chemical reactions.
  • 26. Does Stainless Steel Corrodes ?
  • 27. Ferrous oxide doesn’t form a continuous layer on the steel because the oxide molecule has a larger volume than the underlying iron atoms, and eventually spalls off leaving fresh steel exposed which then starts a deleterious rusting cycle.
  • 28.
  • 29. So Al should corrode more ?  Aluminium corrodes and an Aluminium Oxide (Al2O3) layer forms which is impervious (Doesn't allowing fluid to pass through)
  • 30. Prevent Corrosion 1. Galvanising This is when the zinc layer stops oxygen/water or salt from attacking the iron. An advantage is that a scratch will still slow corrosion (as Zn is higher in the series) via sacrificial protection.
  • 31.  Coatings generally protect the metal by imposing a physical barrier between the metal substrate and the environment.  Three common types of coatings are organic, inorganic, and metallic. Using paint or grease physically stops oxygen/water/salt from reaching the metal like this 2. Coatings (Painting/ Greasing)
  • 32. 3. Electroplating This process deposits a thin layer of metal on the object being protected. Tin plating requires the object being protected to be the negative terminal and surrounded by a solution of the ions of the metal being deposited on to the object. The negative charge attracts positive ions.
  • 33. 4. Sacrificial Protection This method works by taking a metal higher up the reactivity series is connected to the iron/steel and donates its electrons to any iron ions that might have formed, stopping it from corroding.
  • 34. 5. Alloying: Corrosion can be also prevented by alloying some metals with other metals. The resultant metals called alloys do not corrode easily, e.g. stainless steel Austenitic S.S Max. of 0.15% carbon Min 16% chromium Sufficient Ni
  • 35.  According to them, the relatively pure composition of the iron used, presence of high amounts of phosphorus (as much as 1 per cent against less than 0.05 per cent in today's iron) and absence of sulphur/magnesium in the iron are the main reasons for its longevity. Iron Pillar Of Delhi Proudly Standing Since 402 CE (1600 years)