Crystal growth mechanisms additives

The properties described above have important consequences for the way in which these skeletal tissues are subsequently preserved, and hence their usefulness or otherwise as recorders of dietary signals. Several points from the discussion above are relevant here. It is useful to ask what are the most important mechanisms or routes for change in buried bones and teeth One could divide these processes into those with simple addition of new non-apatitic material (various minerals such as pyrites, silicates and simple carbonates) in pores and spaces (Hassan and Ortner 1977), and those related to change within the apatite crystals, usually in the form of recrystallization and crystal growth. The first kind of process has severe implications for alteration of bone and dentine, partly because they are porous materials with high surface area initially and because the approximately 20-30% by volume occupied by collagen is subsequently lost by hydrolysis and/or consumption by bacteria and the void filled by new minerals. Enamel is much denser and contains no pores or Haversian canals and there is very, little organic material to lose and replace with extraneous material. Cracks are the only interstices available for deposition of material. 

The use of tailor made additives holds great promise in the area of crystal growth and morphology control. The routine selection and use of these type of additives will require a fundamental understanding of the mechanism which the additives work on a molecular basis. At the same time, the effect of solvent molecules on the crystal growth process is another related and important problem. In both instances, the relationship between internal aystal structure, aystal growth rate, solvent and impurities are needed to predict the habit of a crystal and thus allow seleaion of the proper conditions and components required to obtain a desired habit... 

For the ion-by-ion reaction, nucleation is generally slower and the density of nuclei smaller. Additionally, growth occurs (ideally) only at a solid surface therefore nucleation is confined to two dimensions, in contrast to three dimensions for the cluster mechanism. The crystal growth may terminate when adjacent crystals touch each other or by some other termination mechanism, e.g., adsorption of a surface-active species. These factors should be valid regardless of whether the mechanism proceeds via free chalcogenide ions or by a complex-decomposition mechanism. 

---