Quick
Search: 
 
advanced search
 GSW Home    GeoRef Home    My GSW Alerts    Contact GSW    About GSW    Journals List    Help 
Clays and Clay Minerals Email Content Delivery
JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS

Clays and Clay Minerals; April 2005; v. 53; no. 2; p. 179-189; DOI: 10.1346/CCMN.2005.0530208
© 2005 Clay Minerals Society
This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (7)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schingaro, E.
Right arrow Articles by Pedrazzi, G.
Right arrow Search for Related Content
GeoRef
Right arrow GeoRef Citation

CATION-SITE PARTITIONING IN Ti-RICH MICAS FROM BLACK HILL (AUSTRALIA): A MULTI-TECHNICAL APPROACH

Emanuela Schingaro1, Fernando Scordari1, Ernesto Mesto1, Maria Franca Brigatti2 and Giuseppe Pedrazzi3

1 Dipartimento Geomineralogico, Universita’ di Bari, via E. Orabona 4, I-70125 Bari, Italy
2 Dipartimento di Scienze della Terra, Universita’ di Modena e Reggio Emilia, P.zza S. Eufemia 19, I-41100 Modena, Italy
3 Dipartimento di Sanita’ Pubblica, Sezione di Fisica, Plesso Biotecnologico Integrato via Volturno 39, I-43100 Parma, Italy

* E-mail address of corresponding author: f.scordari{at}geomin.uniba.it

The crystal chemistry of Ti-rich trioctahedral micas of plutonic origin, cropping out at Black Hill (South Australia) has been investigated by combining electron microprobe analysis, single crystal X-ray diffraction, Mössbauer spectroscopy and X-ray photoelectron spectroscopy. Chemical analyses have shown the samples taken to be quite homogeneous and Ti-rich (TiO2 {approx} 7 wt.%).Mössbauer investigation yielded Fe2+/Fe3+ {approx} 30. X-ray photoelectron spectroscopy analysis seems to suggest the occurrence of three Ti species: octahedral Ti4+(60%), octahedral Ti3+(26%), and tetrahedral Ti4+(14%). The analyzed sample belongs to the 1M polytype and the relevant crystal data from structure analysis are: a = 5.347(1) Å, b = 9.261(2) Å, c = 10.195(2) Å, ß = 100.29° (1). Anisotropic structure refinement was performed in space group C2/m, and converged at R = 2.62, Rw = 2.80. Structural details (the c cell parameter, the off-center shift of the M2 cation towards O4, the bond-length distortions of the cis-M2 octahedron, the interlayer sheet thickness, the projection of K–O4 distance along c*, the difference <K–O>outer–<K–O>inner) support the occurrence of the Ti-oxy substitution (VIR2+ + 2(OH) {rightleftharpoons} VITi4+ + 2O2– + H2) in the sample. Analysis of structural distortions as a function of the Ti content revealed that the positions of the oxygens O3 and O4 are displaced in opposite senses along [100]. This produces an enlargement of the M1 site with respect to the M2 site and a shortening of the interlayer distance. This trend seems to be in common with other Ti-rich 1M micas of plutonic origin.

Key Words: Crystal Chemistry • Mössbauer Investigation • Structure Refinement • Ti Substitutions • Trioctahedral Micas 1M • XPS Investigation




This article has been cited by other articles:


Home page
American MineralogistHome page
M. F. Brigatti, D. Malferrari, M. Poppi, A. Mottana, G. Cibin, A. Marcelli, and G. Cinque
Interlayer potassium and its neighboring atoms in micas: Crystal-chemical modeling and XANES spectroscopy
American Mineralogist, May 1, 2008; 93(5-6): 821 - 830.
[Abstract] [Full Text] [PDF]


Home page
American MineralogistHome page
G. Ventruti, M. Zema, F. Scordari, and G. Pedrazzi
Thermal behavior of a Ti-rich phlogopite from Mt. Vulture (Potenza, Italy): An in situ X-ray single-crystal diffraction study
American Mineralogist, April 1, 2008; 93(4): 632 - 643.
[Abstract] [Full Text] [PDF]


Home page
American MineralogistHome page
R. Sassi, G. Cruciani, C. Mazzoli, L. Nodari, and J. Craven
Multiple titanium substitutions in biotites from high-grade metapelitic xenoliths (Euganean Hills, Italy): Complete crystal chemistry and appraisal of petrologic control
American Mineralogist, February 1, 2008; 93(2-3): 339 - 350.
[Abstract] [Full Text] [PDF]


Home page
American MineralogistHome page
S. Matarrese, E. Schingaro, F. Scordari, F. Stoppa, G. Rosatelli, G. Pedrazzi, and L. Ottolini
Crystal chemistry of phlogopite from Vulture-S. Michele Subsynthem volcanic rocks (Mt. Vulture, Italy) and volcanological implications
American Mineralogist, February 1, 2008; 93(2-3): 426 - 437.
[Abstract] [Full Text] [PDF]


Home page
Mineral MagHome page
E. Schingaro, F. Scordari, S. Matarrese, E. Mesto, F. Stoppa, G. Rosatelli, and G. Pedrazzi
Phlogopite from the Ventaruolo subsynthem volcanics (Mt Vulture, Italy): a multi-method study
Mineralogical Magazine, October 1, 2007; 71(5): 519 - 537.
[Abstract] [Full Text] [PDF]


Home page
Eur J MineralHome page
F. SCORDARI, G. VENTRUTI, A. SABATO, F. BELLATRECCIA, G. DELLA VENTURA, and G. PEDRAZZI
Ti-rich phlogopite from Mt. Vulture (Potenza, Italy) investigated by a multianalytical approach: substitutional mechanisms and orientation of the OH dipoles
European Journal of Mineralogy, June 1, 2006; 18(3): 379 - 391.
[Abstract] [Full Text] [PDF]


Home page
American MineralogistHome page
E. Mesto, E. Schingaro, F. Scordari, and L. Ottolini
An electron microprobe analysis, secondary ion mass spectrometry, and single-crystal X-ray diffraction study of phlogopites from Mt. Vulture, Potenza, Italy: Consideration of cation partitioning
American Mineralogist, January 1, 2006; 91(1): 182 - 190.
[Abstract] [Full Text] [PDF]




JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2009 by Clay Minerals Society