W. Krause et al., ORTHOWALPURGITE, (UO2)BI4O4(ASO4)(2).2H(2)O, A NEW MINERAL FROM THE BLACK-FOREST, GERMANY, European journal of mineralogy, 7(6), 1995, pp. 1313-1324
The new mineral orthowalpurgite was found associated with preisingerit
e, quartz and anatase on a specimen from the dump of the Schmiedestoll
en, Wittichen, Black Forest, Germany. It forms transparent, yellow, or
thorhombic crystals with 2/m symmetry up to 0.3 mm, tabular parallel t
o {010}, elongated parallel to [100]; crystallographic forms are {010}
,{010},{104}, and {100}; Mohs' hardness 41/2, density(calc.) = 6.51 g
cm(-3). The crystals are brittle, show a conchoidal fracture, and an i
ndistinct cleavage parallel to {001}. Orthowalpurgite is biaxial negat
ive, n(x) = 1.98(2), n(y) = 2.00(2) and n(z) = 2.05 (calculated), 2V(x
) = 70(3)degrees (lambda = 589 nm); orientation: X parallel to c, Y pa
rallel to a, and Z parallel to b. Neither pleochroism nor dispersion w
ere observed. Electron-microprobe analyses gave UO3 17.86 wt.%, Bi2O3
64.21 wt.%, As2O5 16.11 wt.%, H2O (calculated from the idealized formu
la) 2.43 wt.%, Sigma 100.61 wt.% this yielded the empirical formula (b
ased on 16 oxygen atoms) (UO2)(0.92)Bi4.06O3.89(ASO(4))(2.07). 1.99H(2
)0, ideally (UO2)Bi4O4(AsO4)(2.2)H2O The cell parameters are a = 5.492
(1) Angstrom, b = 13.324(2) Angstrom, c = 20.685(3) A, V = 1513.6 Angs
trom(3), space group Pbcm, Z = 4. A crystal structure investigation wa
s performed using single-crystal X-ray data. The refinement converged
at R = 0.080 and R(w) = 0.031 for 999 reflections with sin theta/lambd
a less than or equal to 0.6 Angstrom(-1) [F-o > 2 sigma(F-o)] and 68 v
ariable parameters. The coordination polyhedra around the Bi([4+2])and
Bi-[5+2] atoms are edge- and corner-connected to Bi8O8 layers. The la
yers are interconnected via (UO2)(AsO4)(2) chains to form a three-dime
nsional network. The name orthowalpurgite was chosen to express the st
ructural relationship to the triclinic polymorph walpurgite.