Mineral - Mineral Classes - Silicates

Silicates

The base of unit of a silicate mineral is the 4- tetrahedron. In the vast majority of cases, silicon is in four-fold or tetrahedral coordination with oxygen. In very high-pressure situations, silicon will be six-fold or octahderal coordination, such as in the perovskite structure or the quartz polymorph stishovite (SiO2). In the latter case, the mineral no longer has a silicate structure, but that of that of rutile (TiO2), and its associated group, which are simple oxides. These silica tetrahedra are then polymerized to some degree to create various structures, such as one-dimensional chains, two-dimensional sheets, and three-dimensional frameworks. The basic silicate mineral where no polymerization of the tetrahedra has occurred requires other elements to balance out the base 4- charge. In other silicate structures, different combinations of elements are required to balance out the resultant negative charge. It is common for the Si4+ to be substituted by Al3+ because of similarity in ionic radius and charge; in those case, the 5- tetrahedra form the same structures as do the unsubstituted tetrahedra, but their charge-balancing requirements are different.

The degree of polymerization can be described by both the structure formed and how many tetrahedral corners (or coordinating oxygens) are shared (for aluminium and silicon in tetrahedral sites). Orthosilicates (or nesosilicates) have no linking of polyhedra, thus tetrahedra share no corners. Disilicates (or sorosilicates) have two tetrahedra sharing one oxygen. Inosilicates are chain silicates; single-chain silicates have two shared corners, whereas double-chain silicates have two or three shared corners. In phyllosilicates, a sheet structure is formed which requires three shared oxygens; in the case of double-chain silicates, some tetrahedra must share two corners instead of three as otherwise a sheet structure would result. Framework silicates, or tectosilicates, have tetrahedra that share all four corners. The ring silicates, or cyclosilicates, only need to tetrahedra to share only two corners to form the cyclical structure.

The silicate subclasses are described below in order of decreasing polymerization.

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