Page 45 - A Practical Introduction to Optical Mineralogy
P. 45

SILICATE  MINERALS
         ,
        1  1 1 lcltulised tetrahedral layer of the sheet silicates   Figure 2.3
                                                          (a) Sheet silicates
                                                          (b) sheet silicates,
                                                          the three
                                                           polytypes.







 Key
 0  o'-
 e   Cal+, Na+
 0   Mg2+,  Fe 2 +
 0   Si4+.  Al h   \      I   \
         Ill•  ''i''~'C'- of the tetrahedra all  point in  the same  direction
        1111  til" ca-.e  upwards).  Such a  tetrahedral sheet  may be depicted
        111  'II''' -.cction as:
            \'-----~ _/    or   I    t    \
         Ill  ,  ...,, () layers are  joined together by octahedral laye rs;  either
        (  I I )J I) layers. called  Gibbsite  layers and depicted by the letter G,
        1 1 1 ~ ~ ~ .• 1-1:-0 H) layers. called Brucite layers and depicted by
 double chains viewed at right   I ill  "'Ill' I  13 .
 Figure 2.2
 angles to the c axis: the chains
 Double chain   double chain parallel to the c   are linked together by various   I h)   2 layer unit (I  tetrahedral layer and  I octahedral
 silicates.   axis as occurs in the amphiboles   atoms in  the positions shown   \'i== ==t/   layer; called a  I  :  I  type)
             I   G    I   }
                 ---- 7
             11cxt  I  :  I  unit /
 Phyllosilicates
        111  I   lypc represented by kaolinite - serpentine  is similar with a  B layer replacing the G  layer
 When three oxygens are shared between tetrahedra, phyllosilicates or
 sheet  silicates  result.  The  composition  of  such  a  silicate  sheet  is
 [ Si.0 10 ]  ~- .  Phyllosilicates exhibit 'stacking', in which a sheet of brucite
                           }  3 '''" ,,;, (2 '""'h'd"l '"' I oo"h'd"l; o'll'd '2 ;  llyp<)
 2
 2
 composition containing Mg +, Fe •  and (OH)- ions, or a sheet of gibbsite
 composition  containing  AP •  and  (OH)- ions,  is  stacked  on  to  an   alkali  atoms here - K , Na, etc.
 [  Si.O,o]  silicate  sheet  or  sandwiched  between  two  [ Si 4 0 10 ]  silicate   ---- 7
              next  2  :  I  unit '
 sheets (Fig. 2.3a). Variations in this stacking process give rise to several   111   type  with muscovite , illite and montmorillonite having G  octahedral layers, and biotite
         (  )
 related mineral types called polytypes. Three main polytypes exist, each   Jl  l.tyc t ~: the three layer units are joined together by mo novalent alkah tons. Montmo nllomte
 of which  is  defined by  the repeat distance of a  complete multilayered   IIIIIY  no t possess any ato ms in  this plane and may have an overall  negative  charge.  Water
            lllllkntlc~ may enter the structure  alo ng these inter-unit planes
 unit measured along the crystallographic axis. The 7 A, two layer struc-
 ture includes the mineral kaolin ; the 10 A, three layer structure includes
                  B
 the clay minerals montmorillonite and illite, and also the micas; and the
 14 A, four layer structure includes chlorite. Figure 2.3b gives simplified
                            4 layer unit (2 tetrahedral and 2 octahedral; called a 2  : 2 type)
 detzils  of  the  main  polytypes.  These  multilayer  structures  are  held   I BorG  I
 together by  weakly  bonded cations  (K+,  Na•)  in  the  micas  and other
 10 A and  14 A polytypes.  In some other sheet silicates, only  Vander   I   \
 Waals bonding occurs between these  multilayer structures. The sheet
 silicates cleave easily along this weakly bonded layer, and all of them   tll'\1 2 : 2 unit   (3)  14 A type as represented by chlorite
 32                  33
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