7 Minerals 7
112
determination of crystal structure possible. Prior to this, the
classification of silicates was based on chemical and physical
similarities, which often proved to be ambiguous. Although
many properties of a silicate mineral group are determined
by tetrahedral linkage, an equally important factor is the
type and location of other atoms in the structure.
Silicate minerals can be thought of as three-dimensional
arrays of oxygen atoms that contain void spaces (i.e.,
crystallographic sites) where various cations can enter.
Besides the tetrahedral (4-fold coordination) sites, 6-fold,
8-fold, and 12-fold sites are common. A correlation exists
between the size of a cation (a positively charged ion) and
the type of site it can occupy: the larger the cation, the
greater the coordination, because large cations have more
surface area with which the oxygen atoms can make con-
tact. Tetrahedral sites are generally occupied by silicon
and aluminum; 6-fold sites by aluminum, iron, titanium,
magnesium, lithium, manganese, and sodium; 8-fold sites
by sodium, calcium, and potassium; and 12-fold sites by
potassium. Elements of similar ionic size often substitute
for one another. An aluminum ion, for example, is only
slightly larger than a silicon ion, allowing substitution for
silicon in both tetrahedral and 6-fold sites.
SIlICATe MINerAlS
name colour lustre M
ohs
hard-
ness
specific
gravity
Tectosilicates (three-dimensional networks)
feldspar (for other examples, see feldspar)
orthoclase flesh-red, white
to pale yellow,
red, green
vitreous 6–6½ 2.6