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Iron silicate

Fayalite
Fayalite crystal group - Ochtendung, Eifel, Germany.jpg
Fayalite crystals on substrate. Sample collected from Ochtendung, Eifel, Germany
General
Category Nesosilicate
Formula
(repeating unit)
Fe2SiO4
Strunz classification 9.AC.05
Crystal system Orthorhombic
Crystal class Dipyramidal (mmm)
H-M symbol: (2/m 2/m 2/m)
Space group Pbnm
Unit cell a = 4.8211, b = 10.4779
c = 6.0889 [Å]; Z = 4
Identification
Formula mass 203.771
Color Greenish yellow, yellow-brown, brown; pale yellow to amber in thin section
Crystal habit Commonly granular, compact, or massive
Twinning On [100]; also on [031], as trillings
Cleavage {010} moderate, {100} imperfect
Fracture Conchoidal
Mohs scale hardness 6.5 – 7.0
Luster Vitreous to resinous on fractures
Streak White
Diaphaneity Transparent
Specific gravity 4.392
Optical properties Biaxial (-)
Refractive index nα = 1.731 – 1.824 nβ = 1.760 – 1.864 nγ = 1.773 – 1.875
Birefringence δ = 0.042 – 0.051
Pleochroism Faint
2V angle Measured: 74° to 47°, Calculated: 54° to 66°
References

Fayalite (Fe2SiO4; commonly abbreviated to Fa), also called iron chrysolite, is the iron-rich end-member of the olivine solid-solution series. In common with all minerals in the olivine group, fayalite crystallizes in the orthorhombic system (space group Pbnm) with cell parameters a 4.82 Å, b 10.48 Å and c Å 6.09.

Fayalite forms solid solution series with the magnesium olivine endmember forsterite (Mg2SiO4) and also with the manganese rich olivine endmember tephroite (Mn2SiO4).

Iron rich olivine is a relatively common constituent of acidic and alkaline igneous rocks such as volcanic obsidians, rhyolites, trachytes and phonolites and plutonic quartz syenites where it is associated with amphiboles. Its main occurrence is in ultramafic volcanic and plutonic rocks and less commonly in felsic plutonic rocks and rarely in granite pegmatite. It also occurs in lithophysae in obsidian. It also occurs in medium-grade thermally metamorphosed iron-rich sediments and in impure carbonate rocks.

Fayalite is stable with quartz at low pressures, whereas more magnesian olivine is not, because of the reaction olivine + quartz = orthopyroxene. Iron stabilizes the olivine + quartz pair. The pressure and compositional dependence of the reaction can be used to calculate constraints on pressures at which assemblages of olivine + quartz formed.


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