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{{Infobox mineral
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| name = Cristobalite
| category = Silicate mineral
| boxwidth =
| boxbgcolor =
| image = Cristobalite-Fayalite-40048.jpg
| caption = Cristobalite spheres formed via devitrification (loss of silica) from the obsidian matrix (California, USA) 5.9×3.8×3.8 cm.  
| formula = SiO<sub>2</sub>
| molweight =
| strunz = 04.DA.15
| dana = 75.1.1.1
| symmetry  = Tetragonal (α) [[space group]] P4<sub>1</sub>2<sub>1</sub>2, cubic (β) Fd{{overline|3}}m
| unit cell = a = 4.9709(1) A, c = 6.9278(2) A, Z = 4 (α); <br/>a = 7.166 A, Z = 8 (β)
| color = Colorless, white
| habit = Octahedra or spherulites up to several cm large
| system =
| lattice =
| twinning = on {111}
| cleavage =
| fracture = Conchoidal
| tenacity = Brittle
| mohs = 6–7
| luster = Vitreous
| refractive = n<sub>ω</sub> = 1.487 <br/>n<sub>ε</sub> = 1.484
| opticalprop = Uniaxial (-)
| birefringence = 0.003
| pleochroism = None
| streak = White
| gravity = 2.32–2.36
| density =
| melt = 1713&nbsp;°C (β)<ref name=Deer>Deer, W. A., R. A. Howie and J. Zussman, ''An Introduction to the Rock Forming Minerals'', Logman, 1966, pp. 340–355 ISBN 0-582-44210-9</ref>
| fusibility =
| diagnostic =
| solubility =
| diaphaneity = Transparent
| other =
| references = <ref name=Handbook>[http://rruff.geo.arizona.edu/doclib/hom/cristobalite.pdf Cristobalite]. Handbook of Mineralogy.</ref><ref name=Mindat>[http://www.mindat.org/min-1155.html Cristobalite]. Mindat.</ref><ref name=Webmin>[http://webmineral.com/data/Cristobalite.shtml Cristobalite Mineral Data]. Webmineral.</ref>
}}
 
The [[mineral]] '''cristobalite''' is a high-temperature [[polymorphism (materials science)|polymorph]] of [[silica]], meaning that it has the same chemical formula, [[Silicon dioxide|SiO<sub>2</sub>]], but a distinct crystal structure. Both [[quartz]] and cristobalite are polymorphs with all the members of the quartz group, which also include [[coesite]], [[tridymite]] and [[stishovite]]. Cristobalite occurs as white octahedra or [[spherulites]] in acidic volcanic rocks and in converted diatomaceous deposits in the [[Monterey Formation]] of the US state of California and similar areas. Cristobalite is stable only above 1470&nbsp;°C, but can crystallize and persist [[metastable|metastably]] at lower temperatures.
 
The persistence of cristobalite outside of its thermodynamic stability range occurs because the transition from cristobalite to [[quartz]] or [[tridymite]] is "reconstructive", requiring the breaking up and reforming of the [[silica]] framework. These frameworks are composed of [[silicon|Si]][[oxygen|O]]<sub>4</sub> [[tetrahedra]] in which every oxygen atom is shared with a neighbouring tetrahedron, so that the [[chemical formula]] of silica is [[silicon|Si]][[oxygen|O]]<sub>2</sub>. The breaking of these bonds required to convert cristobalite to tridymite and quartz requires considerable [[activation energy]] and may not happen on a human time frame. Framework silicates are also known as [[silicate minerals|tectosilicates]].
 
There is more than one form of the cristobalite framework. At high temperatures, the structure is [[cubic crystal system|cubic]], Fd{{overline|3}}m, No.227, [[Pearson symbol]] ''cF104.''<ref>{{cite journal|journal=Philosophical Magazine|year=1975 |volume=31|pages=1391–1401 |title=The structures of the b-cristobalite phases of SiO<sub>2</sub> and AlPO<sub>4</sub> |doi=10.1080/00318087508228690 |author=Wright A. F., Leadbetter A. J.}}</ref> A [[tetragonal crystal system|tetragonal]] form of cristobalite (P4<sub>1</sub>2<sub>1</sub>2, No. 92, Pearson symbol ''tP12''<ref>{{cite journal|journal=American Mineralogist|year=1994 |volume=79|pages=9–14|title=The pressure behavior of a cristobalite|author=Downs R. T., Palmer D. C.|url=http://www.geo.arizona.edu/xtal/group/pdf/AM79_9.pdf}}</ref>) occurs on cooling below ca. 250&nbsp;°C at ambient pressure, and is related to the cubic form by a static tilting of the silica tetrahedra in the framework. This transition is variously called the low-high or <math>\alpha-\beta</math> transition. It may be termed "displacive"; i.e., it is not generally possible to prevent the cubic β-form from becoming tetragonal by rapid cooling. Under rare circumstances the cubic form may be preserved if the crystal grain is pinned in a matrix that does not allow for the considerable spontaneous strain that is involved in the transition, which causes a change in shape of the crystal. This transition is highly discontinuous. The exact transition temperature depends on the crystallinity of the cristobalite sample, which itself depends on factors such as how long it has been annealed at a particular temperature.
 
The cubic β-phase consists of dynamically disordered silica tetrahedra. The tetrahedra remain fairly regular and are displaced from their ideal static orientations due to the action of a class of low-frequency [[phonons]] called [[rigid unit mode]]s. It is the "freezing" of one of these rigid unit modes that is the soft mode for the α–β transition.
 
In the α–β phase transition only one of the three degenerate cubic crystallographic axes retains a fourfold rotational axis in the tetragonal form. The choice of axis is arbitrary, so that various [[twins]] can form within the same grain. These different twin orientations coupled with the discontinuous nature of the transition can cause considerable mechanical damage to materials in which cristobalite is present and that pass repeatedly through the transition temperature, such as refractory bricks.
 
When devitrifying silica, cristobalite is usually the first phase to form, even when well outside of its thermodynamic stability range. The dynamically disordered nature of the β-phase is partly responsible for the low enthalpy of fusion of silica.
 
The micrometre-scale spheres that make up precious [[opal]] are made of cristobalite, crystallized [[Metastability in molecules|metastably]] at low temperature.
 
<gallery perrow=2 widths=200px heights=200px>
File:B-cristobal1.png|An idealized model of β-cristobalite, showing corner-bonded [[silicon|Si]][[Oxygen|O]]<sub>4</sub> tetrahedra. In reality the tetrahedra are constantly tumbling.
File:B-cristobal2.png|β-cristobalite viewed along another direction.
File:A-cristobal.png|The crumpled framework of α-cristobalite, related to the β-form by static tilting of the tetrahedra.
File:A-cristobalite.png|Unit cell of α-cristobalite; red spheres are oxygen atoms.
</gallery>
 
==References==
{{reflist}}
 
==Further reading==
* ''American Geological Institute Dictionary of Geological Terms''.
* Durham, D. L., "Monterey Formation: Diagenesis". in: ''Uranium in the Monterey Formation of California''. US Geological Survey Bulletin 1581-A, 1987.
* ''Reviews in Mineralogy and Geochemistry'', vol. 29., ''Silica: behavior, geochemistry and physical applications''. Mineralogical Society of America, 1994.
* R. B. Sosman, ''The Phases of Silica''. (Rutgers University Press, 1965)
 
==External links==
*{{ICSC|0809|08}}
 
{{Silica minerals}}
 
[[Category:Quartz varieties]]

Latest revision as of 18:09, 12 April 2014

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