Ditetragonal dipyramidal class
H-M symbol: (4/m 2/m 2/m)
Space group: P41/mnm
|Unit cell||a = 4.63, c = 9.14 [Å]; Z = 2|
|Color||Yellowish brown, lemon-yellow, brown-black|
|Crystal habit||Fibrous to ﬁne-grained aggregates|
|Mohs scale hardness||6 - 7|
|Luster||Dull to earthy|
|Streak||Canary-yellow to dark brown with a greenish tinge|
|Optical properties||Uniaxial (+)|
|Refractive index||nω = 2.190 nε = 2.330|
|Birefringence||δ = 0.140|
The name of the mineral comes from the localilty of Tripuhy, Ouro Preto, Minas Gerais, Brazil, where it was discovered. Hussak and Prior first described the mineral tripuhyite as an oxide of iron and antimony, and assigned it the composition Fe2Sb2O7. When a mineral with composition FeSbO4 was later discovered in Squaw Creek, New Mexico (US), it was considered erroneously as a new mineral and it was given the name squawcreekite. However, other studies had shown that the original tripuhyite was also FeSbO4. In 2002, the Commission on New Minerals and Mineral Names (CNMMN) of the International Mineralogical Association (IMA), approved the redefinition of tripuhyite as FeSbO4 and the discreditation of squawcreekite.
FeSbO4 exhibits the rutile structure, with a tetragonal unit cell. The cations are octahedrally coordinated to oxygen anions, with the octahedra sharing edges along the c-direction. Fe(III) and Sb(V) cations are distributed in a disordered way over the octahedral sites.
- Handbook of Mineralogy
- Webmineral data
- Hussak, E.; Prior, G. T. (1897). "On Tripuhyite, a New Antimonate of Iron, from Tripuhy, Brazil". Mineralogical Magazine. 11: 302–303. doi:10.1180/minmag.1897.011.53.04.
- Foord, E. E.; P. F. Hlava; J. J. Fitzpatrick; R. C. Erd; R. W. Hinton (1991). Neues Jahrbuch Fur Mineralogie-Monatshefte. 8: 363–384. Missing or empty
- Tavora, E. (1955). "X-ray diffraction powder data for some minerals from Brazilian localities". Anais da Academia Brasileira de Ciencias. 27: 7–27.
- Berlepsch, P.; T. Armbruster; J. Brugger; A. J. Criddle; S. Graeser (2003). "Tripuhyite, FeSbO4, revisited.". Mineralogical Magazine. 67: 31–46. doi:10.1180/0026461036710082.
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