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Rakovanite

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Rakovanite
Well formed rakovanite crystals from the type locality: Sunday Mine, Slick Rock Mining District, San Miguel County, Colorado.
General
CategoryPascoite family
Formula
(repeating unit)
Na3{H3[V10O28]}•15H2O
Strunz classification8.CJ.45
Dana classification40.4.7.4
Crystal systemMonoclinic
Crystal classPrismatic (2/m)
(same H-M symbol)
Space groupP21/n
Unit cella = 12.0248(17),
b = 17.121(3),
c = 18.140(3) Å,
β 106.242(8)°; Z = 4
Identification
ColorOrange
Crystal habitBlocky to prismatic on [100]
FractureConchodial
TenacityBrittle
Mohs scale hardness1
LusterSubadamantine
StreakOrange-yellow
DiaphaneityTransparent
Specific gravity2.407 (calculated)
Optical propertiesBiaxial (+)
Refractive indexα589nm = 1.776(5)
β589nm = 1.803(5)
γ589nm = 1.910(6)
Birefringenceδ = 0.134
PleochroismX light yellow, Y orangish yellow, Z yellowish orange, Z > Y> X
2V angle2Vz540nm =58(1); 2Vz589nm = 56(1); 2Vz650nm =53(1)°
Dispersionr < v, strong parallel
Other characteristicsSurface relief: very high
Orientation: X + b; Z Λ c= 8° in obtuse β
It does not fluorescence in long- or short-wave ultraviolent radiation.
References[1][2]

Rakovanite, Na3{H3[V10O28]}•15H20, is a member of the pascoite family. It is a transparent, brittle mineral occurring in the monoclinic crystal system. It is orange in color and has an orange-yellow colored streak. Rakovanite is soft with a Mohs hardness of 1 and a calculated density of 2.407g cm−3. It does not fluoresce in long- or short-wave ultraviolet radiation. Rakovanite crystals are up to one mm in maximum dimension and vary in habit from blocky to prismatic on [001], commonly exhibiting steps and striations parallel to [001]. Its name honors John Rakovan, professor, Department of Geology and Environmental Earth Science, Miami University, Oxford, Ohio, US.[2]

Occurrence

Rakovanite was found on specimens from the Sunday mine and the West Sunday mine, Slick Rock district, San Miguel County, Colorado, US.[2]

It occurs as crystalline crusts on sandstone fractures in the mine walls of the Sunday and West Sunday mines. The best crystals were found perched on an amorphous dehydrated vanadium phase along with crystals tightly adhered to a corvusite-montroseite matrix.[2]

It forms from the oxidation of montroseite-corvusite assemblages. It is associated calcite, corvusite, hewettite, hughesite, montroseite, munirite, paramontroseite, pascoite, rossite, sherwoodite, and other unidentified vanadium phases as well as at least two other potentially new decavanadate species. It forms aqueous solutions of relatively low pH when water reacts with pyrite in the deposit under ambient temperatures and generally oxidizing near-surface environments.[2]

Atomic arrangement

Rakovanite crystal unit consists of the decavanadate polyanion similar to that found in other decavanadate-bearing mineral. The decavanadate polyanion is formed of ten distorted, edge-sharing octahedra which differs in rakovanite unlike other minerals. It contains three hydrogen atoms, forming a {H3[V10O28]}3- anionic complex. Its individual polyanions are linked to an interstitial complex.[2]

Chemical composition

Oxide wt% Normalized wt% Ideal
Na2O 8.02 (0.40) 6.90 7.15
K2O 0.29 (0.05) 0.25 -
MgO 0.01 (0.01) 0.01 -
CaO 0.04 (0.02) 0.03 -
V2O5 81.2 (1.1) 69.90 69.97
Al2O3 0.04 (0.04) 0.03 -
H2O 22.87 22.87
Total 100.00

Empirical formula (based on V = 10 apfu): (Na2.90K0.07Ca0.01Al0.01)ε2.99{H2.98[V10O28]}•15H2O; the ideal formula is Na3{H3[V10O28]}•15H2O calculated as ideal value for Na3{H3[V10O28]}•15H2O. Composition normalized to 100% using ideal H2O value from crystal structure results.[2]

See also

References

  1. ^ "Rakovanite: Rakovanite mineral information and data". www.mindat.org. Retrieved 2015-12-01.
  2. ^ a b c d e f g Kampf, A. R.; Hughes, J. M.; Marty, J.; Gunter, M. E.; Nash, B. (2011). "Rakovanite, Na3V10O28•15H2O, A New Member of the Pascoite Family with a Protonated Decavanadate Polyanion". The Canadian Mineralogist. 49 (2): 595–604. doi:10.3749/canmin.49.2.595.