04 Concrete Defects Flashcards
What is carbonation and how is it caused?
- Carbonation is the process by which carbon dioxide slowly penetrates concrete and dissolves in water present within its pores, forming a mildly carbolic acidic solution
- This acidic solution reacts with the alkaline calcium hydroxide (one of the components of concrete) to form calcium carbonate
- This results in a pH drop, reducing the alkalinity of the concrete (from more than 12.5 to approximately 8.5)
- This carbonation process progressively moves through the concrete over time
What problems are associated with carbonation?
- The passive layer around reinforcing steel will deteriorate when the pH falls below 10.5
- Therefore, once carbonation reaches any steel, the concrete is insufficiently alkaline to protect the steel’s passive layer and thus becomes ‘active’ (aka depassivation)
- Moisture and oxygen ingressing through the porous concrete can now react with the steel, which may begin to rust and corrode
- If this happens, the steel will expand, which can cause cracking and spalling of the concrete cover, thus compromising its structural integrity
- This also makes it easier for aggressive agents to ingress towards the steel, thus further increasing the rate of corrosion
What factors affect the rate of carbonation?
- Quality and density of the concrete - good quality, well compacted concrete will carbonate at a much slower rate
- Exposure of the building to water and carbon dioxide (permanently wet conditions hinder penetration so carbonation will be low)
- Relative humidity of the atmosphere - carbonation is encouraged where RH is between 25-75% (optimum at 50-75%; anything over 75% usually hinders the rate of carbonation as the excess moisture slows the rate of carbon dioxide entry)
- Temperature - warmer temperatures increase the rate of carbonation (subject to RH)
Is the rate of carbonation greater internally or externally? Why?
The rate of carbonation is usually greater internally due to the higher relative humidity and temperature
Is carbonation more likely to cause corrosion in internal or external concrete? Why?
External concrete, due to the increased presence of moisture and oxygen that can penetrate the carbonated concrete
Under what circumstances is the risk of corrosion through carbonation particularly high?
If poor compaction and strength (perhaps caused by a too high water/cement ratio) is coupled with reinforcement with little cover
How would you identify carbonation?
Visual Appearance:
- Longitudinal cracking along the line of any steel reinforcement (hairline cracking can occur as early as a few months after construction)
- Brown stains as a result of the rusting steel
- Over time, the expansion of rusting steel will result in further cracking and spalling of the surface concrete
Chemical Testing:
- Used to determine depth of carbonation
- Phenolphthalein solution is sprayed onto a fresh sample of the concrete
- Non-carbonated areas will turn pink/purple (alkaline), whereas carbonated areas will remain colourless (neutral pH value due to reduced alkalinity)
- The depth of penetration can then be measured
How can carbonated concrete be addressed?
Firstly consider the likely rate of ongoing deterioration and the required life of the structure to assess the cost effectiveness of different protection and repair strategies
Options:
- Patch Repair
- Re-alkalisation by Diffusion
- Electrochemical Re-alkalisation
- Increase Resistivity
What is the process of patch repairing carbonated concrete?
- Clean surface
- Remove loose concrete
- Remove corrosion (e.g. grit blasting)
- Prime the reinforcement with alkali-based solution
- Reinstate concrete cover using patch repair mortar, sprayed concrete or conventional concrete (for large areas only)
What is the process of remediating carbonated concrete through re-alkalisation by diffusion?
- For concrete that has only suffered minor carbonation
- A thickness of fresh alkaline concrete is applied to the surface of the concrete
- Migration of alkalis from the fresh to the original concrete will allow for gradual re-alkalisation
- Not advisable to rely on this method alone if the average depth of carbonation exceeds 10mm, as moisture from the fresh concrete can ingress and increase the rate of steel corrosion
What is the process of remediating carbonated concrete through electrochemical re-alkalisation?
- A temporary anode mesh is fitted close to the surface of the concrete and is electrically connected to the steel reinforcement (cathode) and a power supply
- An electrolyte (usually a sprayed cellulose fibre) is applied around the anode mesh
- The steel cathode then attracts alkali metal ions towards it, so high alkalinity is restored around the steel
- Process takes approximately 3-10 days
How can you increase the resistivity of carbonated concrete?
- Surface coatings - designed to restrict the penetration of carbon dioxide (must still allow the concrete to dry out)
- Hydrophobic impregnants - designed to repel water
- Sheltering the concrete component - e.g. ventilated external cladding
What is chloride attack?
Chloride attack is the process by which chloride ions are introduced into concrete, which reduces its alkalinity
How can chloride ions be introduced into concrete?
- Introduced as an accelerator during the mixing process (calcium chloride)
- Introduced naturally (e.g. from the use of unwashed marine aggregates)
- Introduced as a result of external contamination (e.g. de-icing salt, exposure to salt spray etc.)
When was it common to introduce chloride ions into concrete as an accelerator?
- Prevalent in the 1950s and 1960s - good for concreting in cold weather as the concrete or mortar would harden quickly, thus developing early resistance to freezing and thawing
- Common until around 1978
What method of introducing chloride ions into concrete can cause the most damage?
External contamination as the concentration can be more erratic and the ions are not chemically bound
What problems are associated with chloride attack?
- Loss of alkalinity of the concrete removes its protective capability to stop any encased steel from oxidising (depassivation)
- Similar to carbonation, moisture and oxygen can then lead to expansion of the steel and cracking and spalling of the concrete cover, thus compromising its structural integrity
- Furthermore, as the chloride ions make contact with the steel and the surrounding passive material, hydrochloric acid is formed
- The hydrochloric acid will then eat away at the steel reinforcement (aka ‘pitting’) and could cause loss of section and serious structural failure
- Where high levels of chloride are present, corrosion of steel can occur even if the concrete is highly alkaline
- Where carbonation is also present, chloride attack can increase the rate of oxidisation of the steel reinforcement
What is meant by the term ‘pitting’?
Localised corrosion that leads to the creation of small holes in the metal
What factors affect the rate of chloride attack?
- Physical characteristics of the concrete - i.e. calcium chloride used as an additive or introduced naturally
- Quality and density - denser concrete will be less porous and therefore decrease the rate at which chloride ions can reach the steel
- Physical condition - e.g. cracks and damage can speed up the transportation of moisture and ions to the steel (freeze thaw cycles can then exacerbate the process further)
- Location - sea walls, marine structures (sea water is a major source of chloride ions), areas where de-icing salts have been used and remain in-situ
How would you identify chloride attack?
Visual Appearance:
- Can induce large cracking or bulging within the concrete of a more localised nature than carbonation
- Black coloured rusting and pitting of the steel where aggressive hydrochloric acid has attacked
- May be more difficult to see as pitting can occur where there is no cracking/spalling of the concrete
Chemical Testing:
- Indicator solution is applied and if the liquid turns brown, significant chlorides are present
- If it turns yellow/white, chlorides may be present and further investigation is required
Laboratory Testing