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Physical and chemical causes of deterioration
Short answer
Physical causes: freezing-thawing, thermal effects, shrinkage, abrasion, erosion, salt crystallization, wetting-drying; all increase permeability. Chemical causes: sulphate attack, alkali-aggregate reaction, acid attack, chloride corrosion, carbonation, leaching, sea water, biological attack. Control by dense concrete, low w/c, proper cement, and curing.
Write down (explain in brief) the physical and chemical causes of concrete deterioration.
Physical causes
Physical causes act by mechanical, thermal or moisture processes without changing the chemical composition of cement paste.
| Cause | Mechanism | Effect and control |
|---|---|---|
| Freezing and thawing | Water in pores freezes, expanding by 9%, causing hydraulic pressure; repeated cycles | Scaling, cracking, D-cracking. Use air entrainment (4 to 7%), low w/c, sound aggregate |
| Thermal effects (temperature cycle, fire) | Differential expansion/contraction; above 300 °C paste loses water, above 500 °C Ca(OH)2 decomposes | Cracking, spalling, loss of strength. Joints, cover, insulation |
| Shrinkage and moisture movement | Drying shrinkage restrained by steel/supports | Cracks, which open the way for aggressive agents. Low w/c, curing, joints |
| Abrasion | Wear by traffic, sliding or rolling | Surface loss in pavements, floors. Hard aggregates, high strength, surface treatments |
| Erosion and cavitation | High velocity water with silt, or vapour bubbles collapsing | Pitting of spillways. Smooth surface, high-strength concrete |
| Salt crystallisation | Salt solution crystallises in pores on drying | Pressure causing scaling and efflorescence. Dense concrete, membranes |
| Wetting and drying | Moisture gradients cause cyclic stress | Cracking and surface deterioration |
All physical processes increase permeability and speed up chemical attack, so low w/c, good curing and compaction help in all of them.
Chemical causes
Chemical causes are the reaction of cement paste or aggregate with substances from outside or inside the concrete.
| Cause | Reaction | Effect and control |
|---|---|---|
| Sulphate attack | Sulphates (soil, groundwater, sea) react with and C3A to form gypsum and ettringite | Expansion, cracking, softening. Use sulphate-resistant cement (IS 12330), PPC, low w/c, dense concrete (IS 456 Table 4) |
| Alkali-aggregate (silica) reaction | Alkalis of cement react with reactive silica of aggregate to form an expansive gel which swells with moisture | Map cracking, pop-outs. Use non-reactive aggregates, low-alkali cement, fly ash |
| Acid attack | Acids dissolve and C-S-H into soluble salts | Loss of material, softening. Dense concrete, protective coatings |
| Chloride attack | Chlorides destroy the passive film of steel | Corrosion of reinforcement. Limit chloride (IS 456 Table 7, 0.6 kg/m for RCC) |
| Carbonation | Lowers pH, then corrosion. Low w/c, cover | |
| Leaching and efflorescence | Soft water dissolves and carries it out | Loss of strength, white deposits |
| Sea water | Combined action of sulphate, chloride, crystallisation, abrasion | Use PPC/slag, w/c 0.45 or less, cover |
| Biological | Bacteria produce sulphuric acid in sewers | Surface erosion |
The rate is controlled by permeability: the denser the concrete, the slower the attack.
✓ Answer checked by Claude Sonnet 5.5
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