Metakaolin is a dehydroxylated form of the clay mineral kaolinite.
Stone that are rich in kaolinite are known as china clay or kaolin, traditionally used in the manufacture of porcelain. The particle size of metakaolin is smaller than cement particles, but not as fine as silica fume.
The quality and reactivity of metakaolin is strongly dependent of the characteristics of the raw material used. Metakaolin can be produced from a variety of primary and secondary sources containing kaolinite:
The T-O clay mineral kaolinite does not contain interlayer cations or interlayer water. The temperature of dehydroxylation depends on the structural layer stacking order. Disordered kaolinite dehydroxylates between 530 and 570 °C, ordered kaolinite between 570 and 630 °C. Dehydroxylated disordered kaolinite shows higher pozzolanic activity than ordered. The dehydroxylation of kaolin to metakaolin is an endothermic process due to the large amount of energy required to remove the chemically bonded hydroxyl ions. Above the temperature range of dehydroxylation, kaolinite transforms into metakaolin, a complex amorphous structure which retains some long-range order due to layer stacking. Much of the aluminum of the octahedral layer becomes tetrahedrally and pentahedrally coordinated. In order to produce a pozzolan (supplementary cementitious material) nearly complete dehydroxylation must be reached without overheating, i.e., thoroughly roasted but not burnt. This produces an amorphous, highly pozzolanic state, whereas overheating can cause sintering, to form a dead burnt, nonreactive refractory, containing mullite and a defect Al-Si spinel. Reported optimum activation temperatures vary between 550 and 850 °C for varying durations, however the range 650-750 °C is most commonly quoted. In comparison with other clay minerals kaolinite shows a broad temperature interval between dehydroxylation and recrystallization, much favoring the formation of metakaolin and the use of thermally activated kaolin clays as pozzolans. Also, because the octahedral layer is directly exposed to the interlayer (in comparison to for instance T-O-T clay minerals such as smectites), structural disorder is attained more easily upon heating.