“…King (1973) interpreted the square law in terms of a proposed pre-equilibrium between the predominant [Al(OH) 4 ] − species and a dimeric species at the gibbsite surface; using a linear growth model, the slowness of the reaction was interpreted as due to a very low equilibrium concentration of the dimer at the growing solid surface. This appears to be consistent with the hypothesis of a dimeric "growth unit" which has been proposed (Paulaime et al, 2003;Seyssiecq et al, 1999) based on molecular modelling and crystallographic considerations (the "growth unit" concept in crystallization hypothesises the formation in solution of a fundamental building block of the crystal which can readily be incorporated into the crystal surface (Li et al, 1999;Zhong et al, 1994)). However other authors have proposed different growth units for gibbsite.…”