2014
Hloušekite, (Ni,Co)Cu-4(AsO4)(2)(AsO3OH)(2)(H2O)(9), a new member of the lindackerite supergroup from Jachymov, Czech Republic
PLÁŠIL, Jakub, Jiří SEJKORA, Radek ŠKODA, Milan NOVÁK, Anatoly V KASATKIN et. al.Základní údaje
Originální název
Hloušekite, (Ni,Co)Cu-4(AsO4)(2)(AsO3OH)(2)(H2O)(9), a new member of the lindackerite supergroup from Jachymov, Czech Republic
Autoři
PLÁŠIL, Jakub (203 Česká republika, garant), Jiří SEJKORA (203 Česká republika), Radek ŠKODA (203 Česká republika, domácí), Milan NOVÁK (203 Česká republika, domácí), Anatoly V KASATKIN (643 Rusko), Pavel ŠKACHA (203 Česká republika), František VESELOVSKY (203 Česká republika), Kristýna FEJFAROVÁ (203 Česká republika) a Petr ONDRUŠ (203 Česká republika)
Vydání
Mineralogical Magazine, London, Mineralogical Society, 2014, 0026-461X
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10500 1.5. Earth and related environmental sciences
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.026
Kód RIV
RIV/00216224:14310/14:00079323
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000348531400016
Klíčová slova anglicky
hloušekite; new mineral; arsenate; lindackerite supergroup; lindackerite group; ondrusite group; crystal structure
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 8. 4. 2015 15:25, Ing. Andrea Mikešková
Anotace
V originále
Hloušekite, (Ni,Co)Cu-4(AsO4)(2)(AsO3OH)(2)(H2O)(9), is a new supergene arsenate mineral from the Geister vein (Rovnost mine), Jachymov (St Joachimsthal), Western Bohemia, Czech Republic. It was found along with veselovskyite, pradetite, lavendulan, arsenolite, babanekite and gypsum on the surface of strongly altered ore fragments containing dominant tennantite and chalcopyrite. Hlous. ekite forms thin, lath-like crystals, locally elongated reaching up to 3 mm across. It is transparent, has a pale green colour with vitreous lustre, has a greyish-white streak and it is very brittle with an uneven fracture. It does not fluoresce under shortwave or longwave ultraviolet radiation. Cleavage on {010} is perfect; the Mohs hardness is 2-3. The calculated density is 3.295 g cm(-3). Hlous. ekite is optically biaxial with alpha' = 1.653(2) and gamma' = 1.73. The estimated optical orientation is gamma' vs. elongation (c) = 14(1)degrees. In larger grains it is weakly to moderately pleochroic (alpha = colourless, gamma = pale green to green). Hlousekite is triclinic, space group P (1) over bar, a = 6.4010(6), b = 8.0041(6), c = 10.3969(14) angstrom, alpha = 85.824(8), beta = 79.873(9), gamma = 84.655(7)degrees and V = 521.23(10) angstrom(3), with Z = 1, a:b:c = 0.800: 1: 1.299. The eight strongest lines in the powder X-ray diffraction (XRD) pattern [ d in angstrom (I)(hkl)] are 10.211(100)(001), 7.974(9)(010), 3.984(6)(020), 3.656(5)(1 (1) over bar2), 3.631(5)(0 (2) over bar1), 3.241(5)(022), 3.145(5)(200) and 3.006(5)(210). Chemical analysis by electron microprobe yielded MgO 0.20, FeO 0.10, NiO 5.79, CoO 1.80, CuO 29.53, ZnO 0.66, Al2O3 0.14, P2O5 0.11, As2O5 45.01, H2O 17.71 (calc.), for a total of 101.05 wt.%. The resulting empirical formula, calculated by stoichiometry (9H(2)O + 2OH), obtained from the crystal structure, is (Ni0.79Co0.25)(Sigma 1.04)(Cu3.78Zn0.08Mg0.05Al0.03Fe0.01)(Sigma 3.95) (AsO4)(1. 98)(PO4)(0.02)(AsO3OH)(2.00)(H2O)(9.00). The ideal endmember formula, NiCu4(AsO4)(2)(AsO3OH)(2)(H2O)(9.00), requires NiO 7.23, CuO 30.81, As2O5 44.51, H2O 17.45, total 100.00 wt.%. The crystal structure of hlous. ekite was solved by charge flipping from single-crystal XRD data and refined to R-1 = 0.0599 for 1441 reflections with [I-obs > 3 sigma(I)]. Hlousekite is a new member of the lindackerite group (also including lindackerite, pradetite and veselovskyite) of the lindackerite supergroup. The ondrusite group of the lindackerite supergroup includes ondrus. ite, chudobaite, geigerite and klajite. The establishment of these two groups reflects the difference between the crystal structures of their members, mainly in the coordination environment of the Me cations.