In the absence of elements other than calcium, aluminium, iron and oxygen, calcium aluminoferrite forms a solid solution series of formula Ca22O5 for all values of x in the range 0–0.7. Compositions with x > 0.7 do not exist at ordinary pressures. The crystal is orthorhombic, and is normally lath-like. Its density varies from 4026 kg⋅m−3 to 3614 kg⋅m−3. All compositions melt incongruently in the range 1400−1450 °C. They are ferromagnetic, progressively more so as iron content increases. These phases are easily prepared from the oxides.
In Portland cement clinker, calcium aluminoferrite occurs as an "interstitial phase", crystallizing from the melt. Its presence in clinker is solely due to the need to obtain liquid at the peakkiln processing temperature, facilitating the formation of the desired silicate phases. Apart from this benefit, its effects on cement properties are little more than those of a diluent. Its forms an impure solid solution that deviates markedly in composition from the simple chemical formula. The calcium aluminoferrite phase acts as a repository for many of the minor elements in the clinker. Most of the transitional elements in the cement are found in the ferrite phase, notably titanium, manganese and zinc. There is also a substantial amount of magnesium and silicon, and because of this, oxides other than CaO, Al2O3 and Fe2O3 often make up 15% of the mass of the calcium aluminoferrite. This substitution reduces the melting point to around 1350 °C. Typical chemical compositions for various clinker bulk Fe2O3 contents are:
Oxide
Mass %
Mass %
Mass %
Fe2O3 in Clinker
0.29
2.88
4.87
SiO2
4.0
2.6
6.1
Al2O3
20.2
20.8
17.0
Fe2O3
24.5
23.9
27.7
CaO
44.6
46.4
40.2
MgO
3.7
3.1
4.9
Na2O
0.1
0.1
0.1
K2O
0.1
0.1
0.1
TiO2
1.9
2.7
1.7
Mn2O3
0.1
0.3
1.5
ZnO
1.1
0.1
0.9
Behavior in cements
Calcium aluminoferrite has little effect upon the physical properties of cement. On hydration it forms 4CaO⋅Al2O3⋅nH2O and hydrated iron oxidegel. In principle, this is a fast and energetic reaction, but precipitation of an insoluble layer of hydratediron oxide upon the calcium aluminoferrite crystal surface forms a barrier to further reaction. In the case of Portland cement, subsequent slow reaction with dissolved sulfate forms an AFm phase, which has negligible strength-giving properties. In the case of calcium aluminate cements, the situation is less clear-cut, but there is little contribution to early strength. Calcium aluminoferrite is also present in sulfoaluminate cements, and again contributes no strength.
