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CORROSION
Definition
 Degradation of a metal by its surrounding chemicals
through a chemical reaction on the surface of the
metal.
 An oxidation process.
 Causes loss of metal.
Chemical theory of corrosion
 Corrosion of a metal is due to direct reaction of
atmospheric gases like oxygen, halogens, oxides
of sulphur, oxides of nitrogen, hydrogen sulphide
and fumes of chemicals with metal.
 Oxygen is mainly responsible for the corrosion of
most metallic substances.
Chemical theory of corrosion
 Types:
 Dry corrosion
 Wet corrosion
 Dry corrosion : Certain metals directly react with
oxygen in the absence of moisture.
 Alkali and alkaline earth metals react with oxygen at
room temperature, while some metals react with
oxygen at higher temperature.
 Metals like Ag, Au and Pt are not oxidised as they are
noble metals.
Chemical theory of corrosion
 Dry corrosion : Certain metals directly react with
oxygen in the absence of moisture.
 Alkali and alkaline earth metals react with oxygen at
room temperature, while some metals react with
oxygen at higher temperature.
 Metals like Ag, Au and Pt are not oxidised as they are
noble metals.
Chemical theory of corrosion
Chemical theory of corrosion
Wet / electrochemical corrosion
 Common type of corrosion of metal in aqueous corrosive
environment.
 This type of corrosion occurs when the metal comes
in contact with a conducting liquid or when two
dissimilar metals are immersed or dipped partly in a
solution (electrolyte).
 Formation of a galvanic cell on the surface of metals.
 Some parts of the metal surface act as anode and rest
act as cathode.
 The chemical in the environment and humidity acts as an
electrolyte.
Wet / electrochemical corrosion (cont.)
 Example : Corrosion of iron.
 Oxidation of metal takes place at anode while the
reduction process takes place at cathode.
 By taking rusting of iron as an example, the
reaction can be explained as that it may occur in
two ways:
 (i) evolution of hydrogen and
 (ii) absorption of oxygen.
Wet / electrochemical corrosion (cont.)
 At anode: oxidation occurs.
 At cathode:
 The hydrogen ions (H + ) are formed due to the acidic
environment and the following reaction occurs in the
absence of oxygen
 2H+ + 2e → H2 ↑ (reduction)
 The overall reaction is Fe + 2H+ → Fe+2 + H2
Wet / electrochemical corrosion (cont.)
 In this case, metals react in the acidic environment
and are dissolved (undergo corrosion) to release H2
gas.
 All metals above hydrogen in electrochemical series
show this type of corrosion.
 In hydrogen evolution type of corrosion, anodic area
is large as compared to its cathodic area.
Galvanic Series
 Electrochemical reactions are predicted by electrochemical
series.
 A metal having higher position can replace (reduce) other
metals that have lower position in the series.
 For example,
 Zn + CuSO4 → ZnSO4 + Cu
 that is, Zn + Cu++ → Zn++ + Cu
 Or in other words, zinc will corrode faster than copper.
 In galvanic series, oxidation potential of metals is arranged in
the
 decreasing order of activity of a series of metals.
 More anodic: Mg, Mg alloys, Zn, Al, Cd, Fe, Pb, Sn, Ni–Mo–Fe
alloys) Brasses, Cu, Ni, Cr–steel alloy, Ag, Ti, Au, Pt towards
noble nature.
Galvanic Corrosion
 Also called bimetallic corrosion.
 When two dissimilar metals are connected and
exposed to an electrolyte, they will form a galvanic
cell.
 The anodic metal will be oxidised and it will undergo
corrosion.
 Zinc and copper metals connected with each other in
an electrolyte medium form a galvanic cell.
 Zinc acts as anode and undergoes corrosion while
cathode will be unaffected.
 At anode: Zn → Zn++ + 2e [Oxidation] corrosion
 At cathode: Cu++ + 2e → Cu [Reduction] unaffected
Differential aeration corrosion
 If a metal rod is dipped in an electrolyte, the portion
dipped in water is poor in oxygen concentration and
works as anode.
 The portion above water acts as cathode.
 The system will act as a concentration cell and the
chemical reactions for zinc dipped in water are given
as:
Inter-granular corrosion
 This corrosion is observed in case of alloys.
 Corrosion product is observed at the boundaries of grains.
 Externally, it is not seen. There is a sudden failure of material
due to this corrosion.
 For example, during the welding of stainless steel (an alloy of
Fe, C, Cr), chromium carbide is precipitated at the grain
boundaries.
 The region adjacent to grain boundaries becomes depleted of
chromium composition and is made anodic with respect to
solid solution within the grains richer in chromium.
 Rapid quenching after heat treatment of a metal is the remedy
of inter-granular corrosion.
Protection from corrosion
 Following methods have been adopted for the
protection of metal from corrosion.
 Cathode and anode protection
 Material selection
 Coatings-metals, organic and non organic
 Proper Design
Protection from corrosion : Cathodic protection
 Underground steel pipes are protected from corrosion by
this method.
 A magnesium rod is fixed near the metal under
protection and both are connected with a conducting
wire.
 Magnesium is more positive than iron and, hence, in
electrochemical cell it acts as anode and the iron acts as
cathode.
 According to the principle of galvanic cell, it is anode that
undergoes oxidation, and, hence, corrosion occurs at
anode saving cathode (iron) from corrosion.
 Thus, magnesium sacrifies itself for saving the iron.
Protection from corrosion : Cathodic protection
Protection from corrosion : Impressed current
cathodic protection
 The object to be protected is made cathode and it is
connected to the negative terminal of a DC (direct
current) source.
 The positive terminal of the source is connected to
the other electrode made of graphite or platinum,
lead or nickel.
 The impressed current opposes the galvanic current
(corrosion current) and, hence, protection from
corrosion takes place.
Protection from corrosion : Cathodic protection
Protection from corrosion : Paint
 A paint is a mechanical dispersion of one or more
pigments in medium (liquid, non-volatile) drying oil and
thinner.
 When a metallic surface is painted, the thinner
evaporates while the drying oil forms a dry pigmented
film after oxidising itself.
 A paint has following qualities:
 (i) it should be spread easily on the surface,
 (ii) it should form a tough, uniform and adherent film,
 (iii) the coating of paint should not crack after drying,
 (iv) it should have high covering power,
 (v) it should neither be oxidised nor reduced in environment and
 (vi) the colour due to point should be shining and stable.

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Chapter5 corrosion

  • 2. Definition  Degradation of a metal by its surrounding chemicals through a chemical reaction on the surface of the metal.  An oxidation process.  Causes loss of metal.
  • 3. Chemical theory of corrosion  Corrosion of a metal is due to direct reaction of atmospheric gases like oxygen, halogens, oxides of sulphur, oxides of nitrogen, hydrogen sulphide and fumes of chemicals with metal.  Oxygen is mainly responsible for the corrosion of most metallic substances.
  • 4. Chemical theory of corrosion  Types:  Dry corrosion  Wet corrosion  Dry corrosion : Certain metals directly react with oxygen in the absence of moisture.  Alkali and alkaline earth metals react with oxygen at room temperature, while some metals react with oxygen at higher temperature.  Metals like Ag, Au and Pt are not oxidised as they are noble metals.
  • 5. Chemical theory of corrosion  Dry corrosion : Certain metals directly react with oxygen in the absence of moisture.  Alkali and alkaline earth metals react with oxygen at room temperature, while some metals react with oxygen at higher temperature.  Metals like Ag, Au and Pt are not oxidised as they are noble metals.
  • 6. Chemical theory of corrosion
  • 7. Chemical theory of corrosion
  • 8. Wet / electrochemical corrosion  Common type of corrosion of metal in aqueous corrosive environment.  This type of corrosion occurs when the metal comes in contact with a conducting liquid or when two dissimilar metals are immersed or dipped partly in a solution (electrolyte).  Formation of a galvanic cell on the surface of metals.  Some parts of the metal surface act as anode and rest act as cathode.  The chemical in the environment and humidity acts as an electrolyte.
  • 9. Wet / electrochemical corrosion (cont.)  Example : Corrosion of iron.  Oxidation of metal takes place at anode while the reduction process takes place at cathode.  By taking rusting of iron as an example, the reaction can be explained as that it may occur in two ways:  (i) evolution of hydrogen and  (ii) absorption of oxygen.
  • 10. Wet / electrochemical corrosion (cont.)  At anode: oxidation occurs.  At cathode:  The hydrogen ions (H + ) are formed due to the acidic environment and the following reaction occurs in the absence of oxygen  2H+ + 2e → H2 ↑ (reduction)  The overall reaction is Fe + 2H+ → Fe+2 + H2
  • 11. Wet / electrochemical corrosion (cont.)  In this case, metals react in the acidic environment and are dissolved (undergo corrosion) to release H2 gas.  All metals above hydrogen in electrochemical series show this type of corrosion.  In hydrogen evolution type of corrosion, anodic area is large as compared to its cathodic area.
  • 12.
  • 13. Galvanic Series  Electrochemical reactions are predicted by electrochemical series.  A metal having higher position can replace (reduce) other metals that have lower position in the series.  For example,  Zn + CuSO4 → ZnSO4 + Cu  that is, Zn + Cu++ → Zn++ + Cu  Or in other words, zinc will corrode faster than copper.  In galvanic series, oxidation potential of metals is arranged in the  decreasing order of activity of a series of metals.  More anodic: Mg, Mg alloys, Zn, Al, Cd, Fe, Pb, Sn, Ni–Mo–Fe alloys) Brasses, Cu, Ni, Cr–steel alloy, Ag, Ti, Au, Pt towards noble nature.
  • 14. Galvanic Corrosion  Also called bimetallic corrosion.  When two dissimilar metals are connected and exposed to an electrolyte, they will form a galvanic cell.  The anodic metal will be oxidised and it will undergo corrosion.  Zinc and copper metals connected with each other in an electrolyte medium form a galvanic cell.  Zinc acts as anode and undergoes corrosion while cathode will be unaffected.
  • 15.  At anode: Zn → Zn++ + 2e [Oxidation] corrosion  At cathode: Cu++ + 2e → Cu [Reduction] unaffected
  • 16. Differential aeration corrosion  If a metal rod is dipped in an electrolyte, the portion dipped in water is poor in oxygen concentration and works as anode.  The portion above water acts as cathode.  The system will act as a concentration cell and the chemical reactions for zinc dipped in water are given as:
  • 17.
  • 18. Inter-granular corrosion  This corrosion is observed in case of alloys.  Corrosion product is observed at the boundaries of grains.  Externally, it is not seen. There is a sudden failure of material due to this corrosion.  For example, during the welding of stainless steel (an alloy of Fe, C, Cr), chromium carbide is precipitated at the grain boundaries.  The region adjacent to grain boundaries becomes depleted of chromium composition and is made anodic with respect to solid solution within the grains richer in chromium.  Rapid quenching after heat treatment of a metal is the remedy of inter-granular corrosion.
  • 19.
  • 20. Protection from corrosion  Following methods have been adopted for the protection of metal from corrosion.  Cathode and anode protection  Material selection  Coatings-metals, organic and non organic  Proper Design
  • 21. Protection from corrosion : Cathodic protection  Underground steel pipes are protected from corrosion by this method.  A magnesium rod is fixed near the metal under protection and both are connected with a conducting wire.  Magnesium is more positive than iron and, hence, in electrochemical cell it acts as anode and the iron acts as cathode.  According to the principle of galvanic cell, it is anode that undergoes oxidation, and, hence, corrosion occurs at anode saving cathode (iron) from corrosion.  Thus, magnesium sacrifies itself for saving the iron.
  • 22. Protection from corrosion : Cathodic protection
  • 23. Protection from corrosion : Impressed current cathodic protection  The object to be protected is made cathode and it is connected to the negative terminal of a DC (direct current) source.  The positive terminal of the source is connected to the other electrode made of graphite or platinum, lead or nickel.  The impressed current opposes the galvanic current (corrosion current) and, hence, protection from corrosion takes place.
  • 24. Protection from corrosion : Cathodic protection
  • 25. Protection from corrosion : Paint  A paint is a mechanical dispersion of one or more pigments in medium (liquid, non-volatile) drying oil and thinner.  When a metallic surface is painted, the thinner evaporates while the drying oil forms a dry pigmented film after oxidising itself.  A paint has following qualities:  (i) it should be spread easily on the surface,  (ii) it should form a tough, uniform and adherent film,  (iii) the coating of paint should not crack after drying,  (iv) it should have high covering power,  (v) it should neither be oxidised nor reduced in environment and  (vi) the colour due to point should be shining and stable.