Penfieldite

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Penfieldite
General
CategoryMinerals
FormulaPb2Cl3(OH)
IMA symbolPfd
Strunz classification03.DC.15
Dana classification10.04.01.01
Crystal systemHexagonal
Crystal classTrigonal Dipyramidal
H-M symbol: 6
Space groupP6
Unit cell5,360.83
Identification
Formula mass537.77
ColorColorless, white, yellowish, bluish
CleavageDistinct/good on {0001}
Mohs scale hardness3–4
LusterAdamantine, greasy
StreakWhite
DiaphaneityTransparent
Specific gravity6.00
DensityMeasured: 5.82 – 6.61
Calculated: 6.00
Optical propertiesUniaxial (+)
Refractive indexnω = 2.130(1)
nε = 2.210(1)
Birefringence0.080
SolubilitySoluble in water

Penfieldite is a rare lead hydroxychloride mineral[1] from the class of halides. It was named after Samuel Lewis Penfield. It has been a valid species before the founding of IMA, and was first published in 1892. It had been grandfathered, meaning the name penfieldite is still believed to refer to a valid species.[2][3] When it was first described by Genth in 1892 from Laurion, Greece, the mineral had the formula of Pb3Cl4O.[1]

Penfieldite grows tabular pyramidal crystals, meaning it is longer instead of being wide, and grows in the shape of a pyramid. It is a secondary mineral, meaning that rock minerals went under transformation due to changes in pressure and temperature, and penfieldite is the newly formed stable mineral after this transformation.[2] Singular crystals are usually striped, and can grow up to 3 cm. Pure penfieldite is colorless, however, due to lattice defects or foreign admixtures, it can be white, yellow or even blue. It mainly consists of lead (77.06%) and chlorine (19.78%), and has a negligible amount of oxygen (2.98%) and hydrogen (0.19%) in it. It does not show any radioactive properties whatsoever.[2] After it is dissolved in water, penfieldite leaves a lead oxychloride residue behind that is yellowish white in color.[3] When heated to 180 °C, a 9c periodicity can be observed, meaning the crystal repeats itself every nine layers in the c crystallographic direction. When further heated to 200 °C and above, the crystals are quickly destroyed.[1]

Classification

Occurrences and localities

References

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