Muestra métricas de impacto externas asociadas a la publicación. Para mayor detalle:
| Indexado |
|
||
| DOI | 10.1180/MINMAG.2013.077.8.06 | ||
| Año | 2013 | ||
| Tipo |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
Paratacamite-(Mg) (IMA 2013-014), Cu3(Mg, Cu)Cl 2(OH)6, is the new Mg-Analogue of paratacamite. It was found near the village of Cuya in the Camarones Valley, Arica Province, Chile. The mineral is a supergene secondary phase occurring in association with anhydrite, atacamite, chalcopyrite, copiapite, dolomite, epsomite, haydeeite, hematite, magnesite and quartz. Paratacamite-(Mg) crystals are rhombs and thick to thin prisms up to 0.3 mm in size exhibiting the forms {201} and {001}. Twinning by reflection on {101} is common. The mineral is transparent with a vitreous lustre, with medium to deep-green colour and light-green streak. Mohs hardness is 3-3½, the tenacity is brittle and the fracture is conchoidal. Paratacamite-(Mg) has one perfect cleavage on {201}. The measured and calculated densities are 3.50(2) and 3.551 g cm-3, respectively. The mineral is optically uniaxial (-) with ε = 1.785(5) and ω > 1.8 and slight pleochroism: O (bluish green) > E (green). Electron-microprobe analyses provided the empirical formula Cu 3(Mg0.60Cu0.38Ni0.01Mn 0.01)Cl2(OH)6. The mineral is easily soluble in dilute HCl. Paratacamite-(Mg) is trigonal, R 3, with cell parameters a = 13.689(1), c = 14.025(1) Å, V = 2275.8(3) Å3 and Z = 12. There is a pronounced sub-cell corresponding to a' ≈ ½a, c' ≈ c in space group R3m. The eight strongest lines in the X-ray powder diffraction pattern are [d obs Å(I)(hkl)]: 5.469(87)(021), 4.686(26)(003), 2.904(34)(401), 2.762(100)(223,042), 2.265(81)(404), 1.819(26)(603), 1.710 (34)(440) and 1.380(19)(446). The structure was refined to R 1 = 0.039 for 480 F o > 4σF reflections. Refinement using interlayer Mg-Cu site scattering factors indicated that Mg is distributed statistically between both interlayer octahedra M1O6 and M2O6. A comparison of the distortions associated with M1O6 and M2O6 octahedra suggest that the sample is near the upper compositional limit for stability of the R3 phase. © 2013 Mineralogical Society.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | Kampf, A. R. | - |
Natural History Museum of Los Angeles County - Estados Unidos
|
| 2 | Sciberras, M. J. | - |
Western Sydney University - Australia
|
| 3 | Leverett, P. | - |
Western Sydney University - Australia
|
| 4 | Williams, P. A. | - |
Western Sydney University - Australia
|
| 5 | Malcherek, T. | - |
Universität Hamburg - Alemania
|
| 6 | Schlüter, J. | - |
Universität Hamburg - Alemania
|
| 7 | Welch, M. D. | - |
The Natural History Museum, London - Reino Unido
|
| 8 | Dini, Maurizio | Hombre | |
| 9 | Donoso, A. A.Molina | - |