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Chloride Attack
Chloride attack is one of the most important aspects while
dealing with durability of concrete. It primarily causes
corrosion of reinforcement. Statistics have indicated that over
40% of failure of structures is due to corrosion of steel.
Concrete and the PassiveLayer
The strongly alkaline nature of Ca(OH)2 (pH of about 13)
prevents the corrosion of the steel by the formation of a thin
protective film of iron oxide on the metal surface. This
protection is known as passivity.
If the concrete is permeable to such an extend that soluble
chlorides penetrate right up to the reinforcement and water &
oxygen is also present, then the corrosion of steel will take
place. This layer can also be lost due to carbonation.
Chloride enters the concrete from the cement, water,
aggregate and sometimes from admixtures. This can also
enter by diffusion from environment if concrete is
permeable.
The Bureau of Indian Standard had specified the maximum
chloride content in cementas 0.1%.
The amount of chloride required for initiating corrosion is
partly dependent on the pH value of the pore water in
concrete. At a pH value less than 11.5 corrosion may occur
without the presence ofchloride.
For corrosion to occur, these elements must be present:
~There must be at least two metals (or two locations on a single
metal) at different energy levels
~ an electrolyte
~ a metallic connection
In reinforced concrete, the rebar may have many separate
areas at different energy levels. Concrete acts as the
electrolyte, and the metallic connection is provided by wire
ties, chair supports, or the rebar itself.
Anodic reactions
Fe Fe ++ + 2 e-
Fe++ + 2(OH)- Fe(OH)2 (FerrousHydroxide)
Fe(OH)2 + 2H20 + 02 Fe(OH)3 ( Ferrichydroxide)
Cathodic reaction
4e- +2H20 + O2 4(OH)-
It can be noticed that no corrosion takes place if the concrete is dry or
probably below relative humidity of 60% because enough water is not
there to promote corrosion. If concrete is fully submersed into water
corrosion does not take place because diffusion of oxygen does not
take place into the concrete. Probably the optimum relative humidity
for corrosion is 70 to 80%.
The passive layer can be lost by carbonation due to reduction in alkalinity
of the concrete.
In the presence of moisture and CO2 reacts as
CO2 +H2O H2CO3 (Dil. Carbonic acid)
H2CO3 +Ca(OH)2 CaCO3 +H2O
H2C03 reacts with Ca(OH)2 and carbonation of concrete takes place. This reduce
the alkalinity of concrete. When pH of concrete reduces below 8.3, then passive
layer destroyed and corrosion takes place.
The products of corrosion occupy a volume as much as six times the original
volume of steel. This exert thrust on cover concrete resulting in cracks, spalling
or delamination of concrete. (It is a result of water entering brick, concrete or
natural stone and forcing the surface to peel, pop out or flakeoff).
Metallurgical Methods : Steel can be made more corrosion resistant by altering
its structure through metallurgical processes such as rapid quenching of the hot
bars by series of water jets or keeping the hot bars for a short time in a water
bath.
Corrosion inhibitors : Corrosion can be prevented or delayed by chemical
method by using certain corrosion inhibiting chemicals such as nitrites,
phosphates, benzonates etc. Calcium nitrite is generally added to concrete
during mixing of concrete.
Galvanising of reinforcement: Galvanising of reinforcement (dipping of steel
in molten zinc) is also effective. The zinc surface reacts with calcium hydroxide
in the concrete to form a passive layer and prevents corrosion.
Cathodic protection : This is extensively used in advanced countries. Due to
high cost and long term monitoring this method is not popular in India.
Coatings to reinforcement: The object of coating to steel bar is to provide a durable
barrier to aggressive material, such as chloride. Fusion bonded epoxy coating is one of
the effective method.
Most soils contain sulphate in the form of calcium, sodium,
potassium and magnesium. They occur in soils or ground
water. Ammonium sulphate is frequently present in
agricultural soil and water from use of fertilizers or from
sewage and industrial effluents.
Decay of organic matters in marshy lands, shallow lakes often
leads to formation of H2S which can be transformed into
sulphuric acid by bacterial action.
Therefore sulphate attack is common occurrence in natural
and industrial situations.
The main reactions of sulphate attack on concrete are as under;
1. Formation of sulphoaluminates (ettringite) by reaction of sulphatesalts
and the C3A- phase incement;
C3A+ 3 CS H2 + 26 H C3A(CS)3H32
Increase in volumeof reaction products causes expansion and spalling.
2.Formation of calcium sulphate (gypsum) in reaction with lime (CH)
formed by hydration of cement
NS + CH + 2H NH + CSH2
Increase in volumeof reaction products causes expansion and spalling.
3. Magnesium sulphate is more aggressive than sodium or calcium salts.
4. There are some other reactionsalso.
Sulphate Attack
Spalling (Concrete flakes)
Spalling
Spalling
Carbon dioxide in air or dissolved in water reacts with hydrated
cement systems.
The main concern is the reaction of carbon dioxide with the lime
(CH) - phase. It gives rise to calcium carbonate;
Ca(OH)2 + CO2 = CaCO3 + H2O.
In severe cases, the C-S-H phase, which gives strength, can also be
attacked.
In all such reactions, OH- is consumed, thus lowering down the pH
of concrete. If pH is lowered very much, protection to steel
reinforcement against corrosion may belost.
Carbonation is highest in pH between 50 to 80 percent.
Carbonation
Carbonation
in concrete
•Chemical reactions between aggregate containing
certain reactive constituents and alkalis (sodium and
potassium salts) and hydroxyl ions released by the
hydration of cement can have deleterious effects on
concrete.
•Granite, granite gneiss and schist, quartzite and
sandstone, containing strained quartz are among
the reactive rocks found in India.
Alkali-Aggregate Reaction
Alkali-silica reaction in concrete
The basic mechanism of corrosion of steel, is an electro-chemical
phenomenon, involving an anode process and a cathode process;
 Anode: Fe  2e- + Fe2+
(Metallic iron)
-
 Cathode: 1/2O + H O +2e  2(OH)-
2 2
In addition, the corrosion undergone by steel is due to combination
of iron and (OH-) ions;
 Fe + 1/2O + H O  Fe2+ + 2(OH)  ironhydroxide
2 2
(rust)
Corrosion of Reinforcement
Corrosion of steel reinforcement in concrete structures
Mechanism of corrosion of steel in concrete
Main Reasons of
Corrosion
Presence of chloride ions – from water for mixing as
well as curing, from aggregates, other ingredients,
from the service environment.
Poor quality of concrete – high permeability,no
control on water/cement ratio.
Low pH value of concrete – mainly due to
carbonation,
Inadequate cover thickness.
Use of Sulphate resisting cement: Use cement with low C3A content is
most effective method. So use sulphate resisting cement which contains less
C3A.
Quality Concrete : A well designed, placed and compacted concrete
exhibit higher resistance to sulphateattack.
Use of air-entrainment: Use of air-entrainment to the extend of about
6% has beneficial effect on sulphate resisting quality. This is probably due to
reduction of segregation, improvement in workability, reduction in bleeding
and in general reduction in permeability of concrete.
Use of pozzolona : Use of pozzolanic materials reduce the permeability.
High Pressure Steam Curing: This improve the resistance of concrete to
sulphate attack.
Use of High Alumina Cement: Use of High Alumina Cement improves
the resistance of concrete to sulphate attack.

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chemicalattackinconcrete-140929051100-phpapp01 (1).pptx

  • 1.
  • 2. Chloride Attack Chloride attack is one of the most important aspects while dealing with durability of concrete. It primarily causes corrosion of reinforcement. Statistics have indicated that over 40% of failure of structures is due to corrosion of steel. Concrete and the PassiveLayer The strongly alkaline nature of Ca(OH)2 (pH of about 13) prevents the corrosion of the steel by the formation of a thin protective film of iron oxide on the metal surface. This protection is known as passivity. If the concrete is permeable to such an extend that soluble chlorides penetrate right up to the reinforcement and water & oxygen is also present, then the corrosion of steel will take place. This layer can also be lost due to carbonation.
  • 3. Chloride enters the concrete from the cement, water, aggregate and sometimes from admixtures. This can also enter by diffusion from environment if concrete is permeable. The Bureau of Indian Standard had specified the maximum chloride content in cementas 0.1%. The amount of chloride required for initiating corrosion is partly dependent on the pH value of the pore water in concrete. At a pH value less than 11.5 corrosion may occur without the presence ofchloride.
  • 4. For corrosion to occur, these elements must be present: ~There must be at least two metals (or two locations on a single metal) at different energy levels ~ an electrolyte ~ a metallic connection In reinforced concrete, the rebar may have many separate areas at different energy levels. Concrete acts as the electrolyte, and the metallic connection is provided by wire ties, chair supports, or the rebar itself.
  • 5.
  • 6. Anodic reactions Fe Fe ++ + 2 e- Fe++ + 2(OH)- Fe(OH)2 (FerrousHydroxide) Fe(OH)2 + 2H20 + 02 Fe(OH)3 ( Ferrichydroxide) Cathodic reaction 4e- +2H20 + O2 4(OH)- It can be noticed that no corrosion takes place if the concrete is dry or probably below relative humidity of 60% because enough water is not there to promote corrosion. If concrete is fully submersed into water corrosion does not take place because diffusion of oxygen does not take place into the concrete. Probably the optimum relative humidity for corrosion is 70 to 80%.
  • 7. The passive layer can be lost by carbonation due to reduction in alkalinity of the concrete. In the presence of moisture and CO2 reacts as CO2 +H2O H2CO3 (Dil. Carbonic acid) H2CO3 +Ca(OH)2 CaCO3 +H2O H2C03 reacts with Ca(OH)2 and carbonation of concrete takes place. This reduce the alkalinity of concrete. When pH of concrete reduces below 8.3, then passive layer destroyed and corrosion takes place. The products of corrosion occupy a volume as much as six times the original volume of steel. This exert thrust on cover concrete resulting in cracks, spalling or delamination of concrete. (It is a result of water entering brick, concrete or natural stone and forcing the surface to peel, pop out or flakeoff).
  • 8.
  • 9. Metallurgical Methods : Steel can be made more corrosion resistant by altering its structure through metallurgical processes such as rapid quenching of the hot bars by series of water jets or keeping the hot bars for a short time in a water bath. Corrosion inhibitors : Corrosion can be prevented or delayed by chemical method by using certain corrosion inhibiting chemicals such as nitrites, phosphates, benzonates etc. Calcium nitrite is generally added to concrete during mixing of concrete. Galvanising of reinforcement: Galvanising of reinforcement (dipping of steel in molten zinc) is also effective. The zinc surface reacts with calcium hydroxide in the concrete to form a passive layer and prevents corrosion. Cathodic protection : This is extensively used in advanced countries. Due to high cost and long term monitoring this method is not popular in India. Coatings to reinforcement: The object of coating to steel bar is to provide a durable barrier to aggressive material, such as chloride. Fusion bonded epoxy coating is one of the effective method.
  • 10. Most soils contain sulphate in the form of calcium, sodium, potassium and magnesium. They occur in soils or ground water. Ammonium sulphate is frequently present in agricultural soil and water from use of fertilizers or from sewage and industrial effluents. Decay of organic matters in marshy lands, shallow lakes often leads to formation of H2S which can be transformed into sulphuric acid by bacterial action. Therefore sulphate attack is common occurrence in natural and industrial situations.
  • 11. The main reactions of sulphate attack on concrete are as under; 1. Formation of sulphoaluminates (ettringite) by reaction of sulphatesalts and the C3A- phase incement; C3A+ 3 CS H2 + 26 H C3A(CS)3H32 Increase in volumeof reaction products causes expansion and spalling. 2.Formation of calcium sulphate (gypsum) in reaction with lime (CH) formed by hydration of cement NS + CH + 2H NH + CSH2 Increase in volumeof reaction products causes expansion and spalling. 3. Magnesium sulphate is more aggressive than sodium or calcium salts. 4. There are some other reactionsalso. Sulphate Attack
  • 15. Carbon dioxide in air or dissolved in water reacts with hydrated cement systems. The main concern is the reaction of carbon dioxide with the lime (CH) - phase. It gives rise to calcium carbonate; Ca(OH)2 + CO2 = CaCO3 + H2O. In severe cases, the C-S-H phase, which gives strength, can also be attacked. In all such reactions, OH- is consumed, thus lowering down the pH of concrete. If pH is lowered very much, protection to steel reinforcement against corrosion may belost. Carbonation is highest in pH between 50 to 80 percent. Carbonation
  • 17. •Chemical reactions between aggregate containing certain reactive constituents and alkalis (sodium and potassium salts) and hydroxyl ions released by the hydration of cement can have deleterious effects on concrete. •Granite, granite gneiss and schist, quartzite and sandstone, containing strained quartz are among the reactive rocks found in India. Alkali-Aggregate Reaction
  • 19.
  • 20. The basic mechanism of corrosion of steel, is an electro-chemical phenomenon, involving an anode process and a cathode process;  Anode: Fe  2e- + Fe2+ (Metallic iron) -  Cathode: 1/2O + H O +2e  2(OH)- 2 2 In addition, the corrosion undergone by steel is due to combination of iron and (OH-) ions;  Fe + 1/2O + H O  Fe2+ + 2(OH)  ironhydroxide 2 2 (rust) Corrosion of Reinforcement
  • 21. Corrosion of steel reinforcement in concrete structures
  • 22. Mechanism of corrosion of steel in concrete
  • 23.
  • 24. Main Reasons of Corrosion Presence of chloride ions – from water for mixing as well as curing, from aggregates, other ingredients, from the service environment. Poor quality of concrete – high permeability,no control on water/cement ratio. Low pH value of concrete – mainly due to carbonation, Inadequate cover thickness.
  • 25. Use of Sulphate resisting cement: Use cement with low C3A content is most effective method. So use sulphate resisting cement which contains less C3A. Quality Concrete : A well designed, placed and compacted concrete exhibit higher resistance to sulphateattack. Use of air-entrainment: Use of air-entrainment to the extend of about 6% has beneficial effect on sulphate resisting quality. This is probably due to reduction of segregation, improvement in workability, reduction in bleeding and in general reduction in permeability of concrete. Use of pozzolona : Use of pozzolanic materials reduce the permeability. High Pressure Steam Curing: This improve the resistance of concrete to sulphate attack. Use of High Alumina Cement: Use of High Alumina Cement improves the resistance of concrete to sulphate attack.