Page 151 - A Practical Introduction to Optical Mineralogy
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THE  NON-SILICATES
                                                Sphalerite
       Figure3.3   Pyrite
 coLouR  Colourless to pale brown or pale yellow.
       Sulphide      Key
 HABIT  Euhedral crystals are common, and siderite is often found as aggregates
       structures (after
 of crystals in  oolitic structures.   Q s
       Vaughan &
 All  other properties similar to calcite  (note extreme birefringence).
       Craig 1978).   e  Fe
 occuRRENCE  Common in  ironstone nodules in Carboniferous argillaceous rocks and
 also in the Jurassic ironstones of central England. In Raasay in the Inner
 Hebrides siderite is  associated with  chamosite.
 Siderite  is  found  in  veins  with  other gangue  minerals  and  metallic
 ores.
 3.3  Sulphides
 In  the structures of sulphide  minerals, sulphur atoms are usually  sur-  Cinnabar   Key
 rounded by metallic atoms (e.g. Cu, Zn, Fe) or the semi-metals (Sb, As   Galena
                                                                 ()  Hg
 or  Bi).  The chemical  bonding  is  usually  considered  to  be  essentially
 covalent.  Although  sulphur  has  a  preference for  fourfold  tetrahedral   Qs
 co-ordination it  is  found  in  a large variety of co-ordination polyhedra
 which  may  be  quite  asymmetric.  Non-stoichiometry,  i.e.  a  variable
 metal : sulphur ratio, is a feature of many sulphide structures, especially
 at  high  temperatures;  complex  ordering  may  result  on  cooling  of a
 non-stoichiometric phase leading, at low temperature, to minerals with
 only  slightly  different  compositions  but  different  structures.  A  good
 example is  that of high  temperature cubic digenite, Cu 2 -xS (x  .;;;  0.2),
 which  is  represented at low  temperatures by  orthorhombic chalcocite
 Cu,S,  orthorhombic djurleite  Cu~, 9 ,S and cubic digenite  Cu~, 8 S.
 Two further possible complexities in sulphide structures are the exis-
 tence of sulphur-sulphur bonds exemplified by the s~- pair in pyrite FeS,
                    Covellite            Key
 (see Fig.  3.3), and the existence of structures that can be considered as
 resulting from a replacement by a semi-metal of half the sulphur in such   0  s
 pairs, e.g.  arsenopyrite FeAsS.
 Most sulphides are opaque but some (e.g. sphalerite when pure zinc
 sulphide)  are  transparent.  Some  are  transparent  for  red  light  (e.g.
 pyragyrite Ag 3 SbS 3 )  or only in  the infra-red (e.g. stibnite Sb,S 3 ). Many
 are semiconductors, which means that they conduct electricity at a high
 temperature  but  not  at  a  low  temperature.  In  fact,  the  optical  and
 physical  properties of many sulphides are best understood if the band
 model  of semiconductors is  applied (see Shuey  1975).
 The structures  of several  common  sulphides  are  illustrated  in  Fig-
 ure 3.3. As is evident from the few examples given, sulphide structures
 can be classified - as are the silicates- into structures based on chains,
 sheets, networks and so on. Although such a classification is of less value
 than for the silicates, consideration of structures in such a way helps to
 explain crystal morphology, cleavage directions etc. of some sulphides.
 The sulphosalts  are  one group of sulphides which  are very  diverse
 chemically and structurally. They contain a semi-metal as well as a metal   co-ordination of ions   linkage of polyhedra
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