A contribution to the crystal chemistry of the voltaite group: solid solutions, Moessbauer and infrared spectra, and anomalous anisotropy

Author(s)
Juraj Majzlan, Hannes Schlicht, Maria Wierzbicka-Wieczorek, Gerald Giester, Herbert Pöllmann, Beatrix Brömme, Stephen E J Doyle, Gernot Buth, Christian Bender Koch
Abstract

Voltaite is a mineral of fumaroles, solfatares, coal-fire gas vents, and acid-mine drainage systems. The nominal composition is K2Fe5 2+Fe3 3+Al(SO4)12·18H2O and the nominal symmetry is cubic, Fd3-c . The tetragonal (I41/acd) superstructure of voltaite is known as the mineral pertlikite. In this study, we investigated 22 synthetic voltaite samples in which Fe2+ was partially or completely replaced by Mg, Zn, Mn, or Cd, by single-crystal and powder X-ray diffraction (both in-house and synchrotron). Two samples contained NH4 + instead of K+. The structure of voltaite is based on a framework defined by kröhnkite-like heteropolyhedral chains which host both M3+ and M2+ in octahedral coordination. Unit cell dimensions of the end-members scale almost linearly with the size of M2+. In the Fe2+-Mg-Zn solid solutions, the Fe2+-Mg and Fe2+-Zn solutions are linear (ideal) in terms of their lattice-parameter variations. The Mg-Zn solid solution, however, is strongly non-ideal. A detailed analysis of the topology of the chains showed that this behavior originates in expansion and contraction of individual M2+-O bonds within the chains. In the Mg-Zn solid solution, some of the M2+-O bonds expand while none contract. In the other solid solutions, expansion of some M2+-O bonds is always compensated by contraction of the other ones. Parts of the nominally cubic crystals are optically anisotropic and their symmetry is found to be tetragonal by single crystal X-ray diffraction measurements. The coexistence of cubic and tetragonal sectors within a single crystal without any detectable difference in their chemical composition is difficult to explain in terms of growth of such composite crystals. Mössbauer and infrared spectra collected on our synthetic crystals conform with previously published data.

Organisation(s)
Department of Mineralogy and Crystallography
External organisation(s)
Friedrich-Schiller-Universität Jena, Martin-Luther-Universität Halle-Wittenberg, Karlsruher Institut für Technologie, University of Copenhagen
Journal
Mineralogy and Petrology
Volume
107
Pages
221-233
No. of pages
13
ISSN
0930-0708
DOI
https://doi.org/10.1007/s00710-012-0254-2
Publication date
2013
Peer reviewed
Yes
Austrian Fields of Science 2012
105113 Crystallography
Portal url
https://ucrisportal.univie.ac.at/en/publications/4a0440e8-7e11-482b-86ce-a456184a0d75