Quick
Search: 
 
advanced search
 GSW Home    GeoRef Home    My GSW Alerts    Contact GSW    About GSW    Journals List    Help 
American Mineralogist Don't get GSW? Talk to your librarian.
JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS

American Mineralogist; August-September; v. 94; no. 8-9; p. 1262-1270; DOI: 10.2138/am.2009.3163
© 2009 Mineralogical Society of America
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 Alert me to new issues of the journal
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by Ballirano, P.
Right arrow Articles by Dogan, A. U.
GeoRef
Right arrow GeoRef Citation

Crystal structure and iron topochemistry of erionite-K from Rome, Oregon, U.S.A.

Paolo Ballirano1,2, Giovanni B. Andreozzi1,3, Meral Dogan4 and A. Umran Dogan5,6,*

1 Dipartimento di Scienze della Terra, Sapienza Università di Roma, P.le A. Moro, 5, I-00185 Rome, Italy
2 CNR-IGAG, Istituto di Geologia Ambientale e Geoingegneria, Sede di Roma, Via Bolognola 7, I-00138 Rome, Italy
3 CNR-IGG, Istituto di Geoscienze e Georisorse, Sede di Roma, P.le A. Moro, 5, I-00185 Rome, Italy
4 Department of Geological Engineering, Hacettepe University, Ankara, Turkey
5 Department of Geological Engineering, Ankara University, Ankara, Turkey
6 Department of Chemical and Biochemical Engineering, The University of Iowa, Iowa City, Iowa 52242, U.S.A.

Correspondence: * E-mail: umran-dogan{at}uiowa.edu

A complete crystal-chemical characterization of erionite-K from Rome, Oregon, was obtained by combining field emission scanning electron microscopy, laboratory parallel-beam transmission powder diffraction, and 57Fe Mössbauer spectroscopy. Rietveld refinement results evidenced that the most striking difference in comparison with the structure of erionite-Ca is significant K at a K2 site(1/2, 0, 0), which is empty in erionite-Ca. In addition, site Ca1 shows low occupancy and Ca3 is vacant. The oxidation and coordination state of Fe, whose occurrence was revealed by chemical analysis, have been clarified by exploiting room- and low-temperature 57Fe Mössbauer spectroscopy. The majority of Fe (95%) was attributed to Fe3+-bearing, superparamagnetic, oxide-like nanoparticles with dimensions between 1 and 9 nm, and the remaining 5% was attributed to hematite particles with size ≥10 nm, both located on the crystal surface.

Key Words: Oregon erionite • erionite-K • crystal structure • iron topochemistry • field emission • scanning electron microscopy • laboratory parallel-beam transmission powder diffraction • Rietveld refinement • 57Fe Mössbauer spectroscopy







JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2009 by Mineralogical Society of America