Tricalcium aluminate

Tricalcium aluminate (3CaO.Al₂O₃) is the most basic of the calcium aluminates. It does not occur in nature, but is an important mineral phase in Portland cement.

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Properties

Pure tricalcium aluminate is formed when the appropriate proportions of finely-divided calcium oxide and aluminium oxide are heated together above 1300°C. The mineral is cubic, with unit cell dimension 1.5263 nm^[1] and has density 3064 kg.m^-3. It melts with decomposition at 1542°C.

In Portland cement clinker, tricalcium aluminate occurs as an "interstitial phase", crystallizing from the melt. Its presence in clinker is solely due to the need to obtain liquid at the peak kiln processing temperature (1400-1450°C), facilitating the formation of the desired silicate phases. Apart from this benefit, its effects on cement properties are mostly undesirable. It forms an impure solid solution phase, with 15-20% of the aluminium atoms replaced by silicon and iron, and with variable amounts of alkali metal atoms replacing calcium, depending upon the availability of alkali oxides in the melt. The impure form has at least four polymorphs:

Typical chemical compositions are:

Effect on cement properties

In keeping with its high basicity, tricalcium aluminate reacts most strongly with water of all the calcium aluminates, and it is also the most reactive of the Portland clinker phases. Its hydration to phases of the form Ca₂AlO₃(OH).nH₂O leads to the phenomenon of "flash set" (instantaneous set), and a large amount of heat is generated. To avoid this, Portland-type cements include a small addition of calcium sulfate (typically 4-8%). Sulfate ions in solution lead to the formation of an insoluble layer of ettringite (3CaO.Al₂O₃.3CaSO₄.32H₂O) over the surface of the aluminate crystals, passivating them. The aluminate then reacts slowly to form the AFm phase 3CaO.Al₂O₃.CaSO₄.12H₂O. These hydrates contribute little to strength development.

Tricalcium aluminate is associated with three important effects that can reduce the durability of concrete:

• heat release, which can cause spontaneous over-heating in large masses of concrete. Where necessary, tricalcium aluminate levels are reduced to control this effect.
• sulfate attack, in which sulfate solutions to which the concrete is exposed react with the AFm phase to form ettringite. This reaction is expansive, and can disrupt mature concrete. Where concrete is to be placed in contact with, for example, sulfate-laden ground waters, either a "sulfate-resisting" cement (with low levels of tricalcium aluminate) is used, or slag is added to the cement or to the concrete mix. The slag contributes sufficient aluminium to suppress formation of ettringite.
• delayed ettringite formation, where concrete is cured at temperatures above the decomposition temperature of ettringite (about 65°C). On cooling, expansive ettringite formation takes place.

Because they are even more basic, the alkali-loaded polymorphs are correspondingly more reactive. Appreciable amounts (>1%) in cement make set control difficult, and the cement becomes excessively hygroscopic. The cement powder flowability is reduced, and air-set lumps tend to form. They withdraw water from gypsum on storage of the cement, leading to false set. For this reason, their formation is avoided wherever possible. It is more energetically favorable for sodium and potassium to form sulfates and chlorides in the kiln, but if insufficient sulfate ion is present, any surplus alkalis congregate in the aluminate phase. The feed and fuel in the kiln system are preferably controlled chemically to keep the sulfate and alkalis in balance. However, this stoichiometry is only maintained if there is substantial surplus oxygen in the kiln atmosphere: if "reducing conditions" set in, then sulfur is lost as SO₂, and reactive aluminates start to form. This is readily monitored by tracking the clinker sulfate level on an hour-to-hour basis.

References

1. ^ H F W Taylor, Cement Chemistry, Academic Press, 1990, ISBN 0-12-683900-X, pp 23