GROUP NO 6

Group Members Name
Waqas Ahmad
Umair Aslam
Tayyab Naveed
Muhammad Umair
Muhammad Mudeser khalid
Mujahid Ali
Definition of Corrosion

Corrosion is the slow process of decay of the
metal, due to the attack of the atmosphere gases
on the surface of the metal, resulting in the
formation of metallic compounds such oxides,
hydroxides, carbonates, sulphides etc.
FORMS OF CORROSION
CORROSION

WET CORROSION

DRY CORROSION

CORROSION

ROOM TEMPERATURE
CORROSION

HIGH TEMPERATURE
CORROSION
1. Dry or Chemical Corrosion:
It is due to the direct chemical action of
environmental atmosphere gases such as O2.
H2S, SO2, N2, halogens or anhydrous
inorganic liquids with metal surfaces.
2. Wet or Electrochemical Corrosion:
It is due to the existence of separate
“anodic” and “cathodic” areas in the system
between which current flows through the
conducting liquid and the anode gets oxidized
and wasted.
WET / AQUEOUS CORROSION
Based on the appearance of the corroded metal,
wet corrosion may be classified as
 Uniform or General
 Galvanic or Two-metal
 Crevice
 Pitting
UNIFORM CORROSION
 Corrosion over the

entire exposed surface
at a uniform rate. e.g..
Atmospheric corrosion.
 Maximum metal loss by
this form.
 Not dangerous. Rate
can be measured in the
laboratory
GALVANIC CORROSION
 When two dissimilar

metals are joined together
and exposed, the more
active of the two metals
corrode faster and the
nobler metal is protected.
This excess corrosion is
due to the galvanic current
generated at the junction
 a) Steel plates with copper
rivets in seawater 15 months.
 b) ) Copper plates with steel
rivets, same environmental
conditions
CREVICE CORROSION
 Intensive localized

corrosion within
crevices & shielded areas
on metal surfaces
 Small volumes of
stagnant corrosive
caused by holes, gaskets,
surface deposits, lap
joints
PITTING
A form of extremely
localized attack
causing holes in the
metal
Most destructive form
Autocatalytic nature
Difficult to detect and
measure
Electrochemical Theory of Corrosion
(Mechanism Of Corrosion)
Corrosion is an electrochemical process.

Galvanic cells are setup between dissimilar metals in contact with each
other or between dissimilar parts of he same metal when surrounded by
moist air or liquid.
Anodic area oxidation takes place
Cathodic area reduction takes place.
Metallic ions formed at the anodic part and ions formed at the
cathodic part diffuses towards each other through conducting
medium and the corrosion product is formed somewhere between
the anodic and cathodic areas.
Anodic iron gets oxidised to Fe2+
M

Mn+ + ne-

The oxygen at the cathode changes to OH- by reduction.
½ O2 + H2O +2e2 OH-
Factors Affecting
Corrosion
Rate & Extent of corrosion
1. The position of metals in the electrochemical Series

More
oxidation

Decreasing
tendency
to loose
electrons

Metal
SRP,
Eo
Lithium
Potassium
Calcium
Sodium
Magnesium
Aluminum
Zinc
Nickel
Tin
Hydrogen--------------- 0.00
Copper
Silver
Platinum
Gold---------------------- +1.15 V

Less
Reduction

Increasing
order of std
reduction
potential
2. Purity of the metal

A pure metal is more corrosion resistant than an
impure metal. The rate and extent of corrosion
increases with the amount of impurities present.
3.Physical state of the metal

Smaller the size of the metal, more the area under
stress and greater is the corrosion.
4. Solubility and volatility of corrosion product

If the product of corrosion is soluble in the
corroding medium and also is volatile, corrosion
occurs faster.
6. Nature of the corroding environment

A.Temperature: Corrosion generally increases
with rise in temperature of environment.
B.Humidity of the air: Rate of corrosion
increases with presence of moisture in the
atmosphere.
C.Impurities: Presence of impurities like CO2,
H2S, SO2, acid fumes etc increases corrosion
rate.
D.Influence of pH: In acid medium corrosion is
more and in alkaline medium it is less.
Prevention of Corrosion
1. Maintaining the purity of the metal
Pure metals are generally corrosion resistant.
2. Alloying with other elements
It to found that alloying with suitable
elements increases corrosion resistance of
most metals.
3. Modification of environment
Deaeration of aqueous environment and
dehumidification decreases the rate of
corrosion.
4 . Protective coatings

1.Metallic Coating
2.Non-metallic coatings
3.Organic coatings
i. Metallic Coating
a) Using less active metal
b) Using a more active metal
ii. Non-Metallic Coating

a) Phosphate coating by Alkaline solution of phosphate.
b) Chromate coating using chromate solutions.
iii. Organic Coating
Plastics, polythene, rubber etc, are used for coating to
prevent corrosion.
Mainly on articles like, ship, submarines. Etc.
ELECTRICAL PROTECTION
Zn2+ + 2e-

Zn

½ O2 + H2O + 2e-

Anode

2OH-

Cathode

Cathod
e
Zn

Anode
THANK
YOU FOR
ATTENTI
ON

Corrosion

  • 2.
    GROUP NO 6 GroupMembers Name Waqas Ahmad Umair Aslam Tayyab Naveed Muhammad Umair Muhammad Mudeser khalid Mujahid Ali
  • 4.
    Definition of Corrosion Corrosionis the slow process of decay of the metal, due to the attack of the atmosphere gases on the surface of the metal, resulting in the formation of metallic compounds such oxides, hydroxides, carbonates, sulphides etc.
  • 5.
    FORMS OF CORROSION CORROSION WETCORROSION DRY CORROSION CORROSION ROOM TEMPERATURE CORROSION HIGH TEMPERATURE CORROSION
  • 6.
    1. Dry orChemical Corrosion: It is due to the direct chemical action of environmental atmosphere gases such as O2. H2S, SO2, N2, halogens or anhydrous inorganic liquids with metal surfaces. 2. Wet or Electrochemical Corrosion: It is due to the existence of separate “anodic” and “cathodic” areas in the system between which current flows through the conducting liquid and the anode gets oxidized and wasted.
  • 7.
    WET / AQUEOUSCORROSION Based on the appearance of the corroded metal, wet corrosion may be classified as  Uniform or General  Galvanic or Two-metal  Crevice  Pitting
  • 8.
    UNIFORM CORROSION  Corrosionover the entire exposed surface at a uniform rate. e.g.. Atmospheric corrosion.  Maximum metal loss by this form.  Not dangerous. Rate can be measured in the laboratory
  • 9.
    GALVANIC CORROSION  Whentwo dissimilar metals are joined together and exposed, the more active of the two metals corrode faster and the nobler metal is protected. This excess corrosion is due to the galvanic current generated at the junction  a) Steel plates with copper rivets in seawater 15 months.  b) ) Copper plates with steel rivets, same environmental conditions
  • 10.
    CREVICE CORROSION  Intensivelocalized corrosion within crevices & shielded areas on metal surfaces  Small volumes of stagnant corrosive caused by holes, gaskets, surface deposits, lap joints
  • 11.
    PITTING A form ofextremely localized attack causing holes in the metal Most destructive form Autocatalytic nature Difficult to detect and measure
  • 12.
    Electrochemical Theory ofCorrosion (Mechanism Of Corrosion) Corrosion is an electrochemical process. Galvanic cells are setup between dissimilar metals in contact with each other or between dissimilar parts of he same metal when surrounded by moist air or liquid. Anodic area oxidation takes place Cathodic area reduction takes place. Metallic ions formed at the anodic part and ions formed at the cathodic part diffuses towards each other through conducting medium and the corrosion product is formed somewhere between the anodic and cathodic areas.
  • 13.
    Anodic iron getsoxidised to Fe2+ M Mn+ + ne- The oxygen at the cathode changes to OH- by reduction. ½ O2 + H2O +2e2 OH-
  • 14.
  • 15.
    1. The positionof metals in the electrochemical Series More oxidation Decreasing tendency to loose electrons Metal SRP, Eo Lithium Potassium Calcium Sodium Magnesium Aluminum Zinc Nickel Tin Hydrogen--------------- 0.00 Copper Silver Platinum Gold---------------------- +1.15 V Less Reduction Increasing order of std reduction potential
  • 16.
    2. Purity ofthe metal A pure metal is more corrosion resistant than an impure metal. The rate and extent of corrosion increases with the amount of impurities present.
  • 17.
    3.Physical state ofthe metal Smaller the size of the metal, more the area under stress and greater is the corrosion.
  • 18.
    4. Solubility andvolatility of corrosion product If the product of corrosion is soluble in the corroding medium and also is volatile, corrosion occurs faster.
  • 19.
    6. Nature ofthe corroding environment A.Temperature: Corrosion generally increases with rise in temperature of environment. B.Humidity of the air: Rate of corrosion increases with presence of moisture in the atmosphere. C.Impurities: Presence of impurities like CO2, H2S, SO2, acid fumes etc increases corrosion rate. D.Influence of pH: In acid medium corrosion is more and in alkaline medium it is less.
  • 20.
  • 21.
    1. Maintaining thepurity of the metal Pure metals are generally corrosion resistant.
  • 22.
    2. Alloying withother elements It to found that alloying with suitable elements increases corrosion resistance of most metals.
  • 23.
    3. Modification ofenvironment Deaeration of aqueous environment and dehumidification decreases the rate of corrosion.
  • 24.
    4 . Protectivecoatings 1.Metallic Coating 2.Non-metallic coatings 3.Organic coatings
  • 25.
    i. Metallic Coating a)Using less active metal b) Using a more active metal
  • 26.
    ii. Non-Metallic Coating a)Phosphate coating by Alkaline solution of phosphate. b) Chromate coating using chromate solutions.
  • 27.
    iii. Organic Coating Plastics,polythene, rubber etc, are used for coating to prevent corrosion. Mainly on articles like, ship, submarines. Etc.
  • 28.
  • 29.
    Zn2+ + 2e- Zn ½O2 + H2O + 2e- Anode 2OH- Cathode Cathod e Zn Anode
  • 31.