Freieslebenite

Freieslebenite is a sulfosalt mineral composed of antimony, lead, and silver. Sulfosalt minerals are complex sulfide minerals with the formula: AmBnSp. The formula of freieslebenite is AgPbSbS3.

Freieslebenite
Freieslebenite from Hiendelaencina, Spain. Exposed in the Mineralogical Museum, Bonn, Germany
General
CategorySulfosalt minerals
Formula
(repeating unit)
AgPbSbS3
IMA symbolFlb[1]
Strunz classification2.JB.15
Crystal systemMonoclinic
Crystal classPrismatic (2/m)
(same H-M symbol)
Space groupP21/n
Unit cella = 7.518(1)
b = 12.809(4)
c = 5.940(1) [Å]
β = 92.25(1)°; Z = 4
Identification
ColorPale steel-gray to silver-white or lead-gray
Crystal habitStriated, prismatic crystals, inclusions and exsolutions in galena and other silver minerals
TwinningTwin plane {010}
Cleavage{110} Indistinct
FractureBrittle-conchoidal
Mohs scale hardness2.5
LusterMetallic
StreakWhitish-gray
DiaphaneityOpaque
Specific gravity6.20-6.23
PleochroismVery weak
References[2][3][4]

Freieslebenite was discovered in approximately 1773 in the Himmelsfurst mines of Freiberg, Saxony, Germany. The mineral was initially called Schilf-Glaserz; however, in 1845 it was given the current name Freieslebenite after the Mining Commissioner of Saxony, Johann Carl Freiesleben (1774–1846).[5]

Structure

Freieslebenite is a superstructure of a PbS-type substructure. The crystal structure is monoclinic with a space group P21/a, with a = 7.518(1), b = 12.809(4), c = 5.940(1) Å, β = 92.25(1)° and Z = 4(Ito, 1973). Sb has a trigonal-pyramidal coordination of S atoms, this structure isolates the SbS3 pyramids from themselves. The Sb–S distances are 2.431, 2.453 and 2.480(4) Å. Six S atoms are coordinated with Pb in a distorted octahedral arrangement. The Pb–S distances range from 2.806 to 3.167(4) Å. Ag has three nearest S neighbors at the distances 2.522, 2.575 and 2.687(4) Å. The AgS3 group is almost planar. A fourth S atom is at a distance of 2.928(4) Å from Ag, the Ag–S being closely perpendicular to the AgS3 plane (Cascarano et al., 1987). The crystal structure of freieslebenite was determined by Wuensch and Nowacki in 1967. Wuensch and Nowacki determined the crystal structure of freieslebenite using three-dimensional counter data, systematic consideration of all possible arrangements permitted by the subcell-supercell relationship and the method of key shifts (Ito, 1973).

Physical properties

Cluster of twinned freieslebenite crystals on quartz matrix from Neue Hoffnung Gottes Mine, Bräunsdorf, Freiberg District, Erzgebirge, Saxony, Germany (Size: 5.6 x 4.4 x 1.9 cm)

Freieslebenite has a metallic luster and is opaque in transparency. The general colors for freieslebenite are gray, silver and white. It has a whitish-gray streak with a hardness of 2.5 on the Mohs scale. It has an imperfect cleavage and an irregular fracture. The density of freieslebenite is 6.20-6.23 g/cm3.

Geologic occurrence

The occurrence of freieslebenite is commonly found in hydrothermal locations. A major finding of freieslebenite was located in the Hiendelaencina mining district in Spain (Frias, 1991). Freieslebenite can also be located in North and South America and throughout Asia and Europe. Deposits of freieslebenite can generally be located in proximity with minerals argentite, siderite, freibergite, polybasite, and aramayoite.

See also

Notes

  1. Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi:10.1180/mgm.2021.43. S2CID 235729616.
  2. Mindat
  3. Handbook of Mineralogy
  4. Webmineral data
  5. (Palache et al., 1944)

References

  • Palache, C., H. Berman, and C. Frondel (1944) Dana's system of mineralogy, (7th edition), v. I, 416–418.
  • Tetsuzo Ito and Werner Nowacki and (1974). The crystal structure of freieslebenite, PbAgSbS3* Zeitschrift für Kristallographie: Vol. 139, No. 1-2, pp. 85–102
  • Frias, Martinez, J. (1991) The Hiendelaecina mining district (Guadalajara, Spain), Instituto Andaluz de Geologia Mediterranea, C.S.I.C
  • G. Cascarano, C. Giacovazzo, M. Luić, A. Pifferi und R. Spagna. (1987) 1-Phase seminvariants and Harker sections II. A new procedure. Zeitschrift für Kristallographie 179:1-4, 113-125
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