TY - JOUR
T1 - Crystal structure and revised chemical formula for burckhardtite, Pb2(Fe3+Te6+)[AlSi3O8]O6
T2 - A double-sheet silicate with intercalated phyllotellurate layers
AU - Christy, Andrew G.
AU - Kampf, Anthony R.
AU - Mills, Stuart J.
AU - Housley, Robert M.
AU - Thorne, Brent
N1 - Publisher Copyright:
© 2014 Mineralogical Society.
PY - 2014/12/1
Y1 - 2014/12/1
N2 - The crystal structure of burckhardite from the type locality, Moctezuma, Sonora, Mexico, has been refined to R 1 = 0.0362 and wR 2 = 0.0370 for 215 reflections with I > 2σ(I). Burckhardtite is trigonal, space group P31m, with the unit-cell parameters a = 5.2566(5) Å, c = 13.0221(10) Å, V = 311.62(5) Å3 and Z = 1 for the ideal formula unit Pb2(Fe3+Te6+)[AlSi3O8]O6. There is no long-range order of (Fe3+, Te6+) or (Al3+, Si4+). New microprobe data were used to estimate site scattering factors, and Raman spectroscopic data showed no evidence of O-H stretching bands. Burckhardtite is not closely related to the micas, as supposed previously, but is a double-sheet silicate in which the aluminosilicate anion resembles that of minerals such as cymrite and kampfite. The [(Fe3+Te6+)O6]3- part of the structure is not bonded directly to the aluminosilicate layer, but forms a discrete anionic phyllotellurate layer that alternates with the [AlSi3O8]- double sheets. Similar phyllotellurate layers are known from several synthetic phases. In burckhardtite, Pb2+ cations intercalate between phyllosilicate and phyllotellurate layers, forming a Pb2[FeTeO6] module that is topologically similar to a slab of the structure of rosiaite, Pb[Sb2O6]. The crystal symmetry, structure, classification as a double-sheet silicate and chemical formula, including the determination of the 6+ valence of Te and absence of essential H2O, are all new findings for the mineral.
AB - The crystal structure of burckhardite from the type locality, Moctezuma, Sonora, Mexico, has been refined to R 1 = 0.0362 and wR 2 = 0.0370 for 215 reflections with I > 2σ(I). Burckhardtite is trigonal, space group P31m, with the unit-cell parameters a = 5.2566(5) Å, c = 13.0221(10) Å, V = 311.62(5) Å3 and Z = 1 for the ideal formula unit Pb2(Fe3+Te6+)[AlSi3O8]O6. There is no long-range order of (Fe3+, Te6+) or (Al3+, Si4+). New microprobe data were used to estimate site scattering factors, and Raman spectroscopic data showed no evidence of O-H stretching bands. Burckhardtite is not closely related to the micas, as supposed previously, but is a double-sheet silicate in which the aluminosilicate anion resembles that of minerals such as cymrite and kampfite. The [(Fe3+Te6+)O6]3- part of the structure is not bonded directly to the aluminosilicate layer, but forms a discrete anionic phyllotellurate layer that alternates with the [AlSi3O8]- double sheets. Similar phyllotellurate layers are known from several synthetic phases. In burckhardtite, Pb2+ cations intercalate between phyllosilicate and phyllotellurate layers, forming a Pb2[FeTeO6] module that is topologically similar to a slab of the structure of rosiaite, Pb[Sb2O6]. The crystal symmetry, structure, classification as a double-sheet silicate and chemical formula, including the determination of the 6+ valence of Te and absence of essential H2O, are all new findings for the mineral.
KW - Crystal structure
KW - burckhardtite
KW - double-sheet silicate
KW - moctezuma
KW - phyllosilicate
KW - phyllotellurate
UR - http://www.scopus.com/inward/record.url?scp=84946026619&partnerID=8YFLogxK
U2 - 10.1180/minmag.2014.078.7.18
DO - 10.1180/minmag.2014.078.7.18
M3 - Article
SN - 0026-461X
VL - 78
SP - 1763
EP - 1773
JO - Mineralogical Magazine
JF - Mineralogical Magazine
IS - 7
ER -