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; October 2009; v. 94; no. 10; p. 1351-1360; DOI: 10.2138/am.2009.3183
© 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 Nagashima, M.
Right arrow Articles by Akasaka, M.

A crystal-chemical investigation of clinozoisite synthesized along the join Ca2Al3Si3O12(OH)-Ca2Al2CrSi3O12(OH)

Mariko Nagashima1,2,*, Charles A. Geiger1 and Masahide Akasaka3

1 Institut für Geowissenschaften, Abteilung Mineralogie, Christian-Albrechts-Universität zu Kiel, D-24098 Kiel, Germany
2 Mineralogical Crystallography, Institute of Geological Sciences, University of Bern, Freiestrasse 3, CH-3012 Bern, Switzerland
3 Department of Geoscience, Faculty of Science and Engineering, Shimane University, Matsue 690-8504, Japan

Correspondence: * E-mail: mariko.nagashima{at}krist.unibe.ch

Cr3+-bearing clinozoisite along the join Ca2Al3Si3O12(OH)-Ca2Al2Cr3+Si3O12(OH) was synthesized using cold-seal pressure vessels at PH2O = 0.35 to 0.40 GPa and T = 500 °C and a piston-cylinder apparatus at PH2O = 0.8 to 1.5 GPa and T = 500 to 800 °C. Gel-starting materials of Ca2Al3–qCr3+qSi3O12.5 composition with q = 1.00, 0.75, 0.50, and 0.25 were employed to maximize the yields of clinozoisite. Mass fractions of clinozoisite in the experimental products with q = 0.50, 0.75, and 1 were about 70 to 90% along with lesser amounts of eskolaite, garnet, and quartz. Clinozoisite crystallized from the gel with q = 0.25 was associated only with zoisite. The crystal structures of clinozoisite in four runs, containing 0.28, 0.49, 0.50, and 0.62 Cr apfu were refined using X-ray powder diffraction data and the Rietveld method. The amount of Cr3+ at the octahedral M3 and M1 sites ranged from 0.37(1)–0.16(1) to 0.25(1)–0.12(1) apfu, respectively. Corresponding KD = (Cr3+/Al)M1/(Cr3+/Al)M3 values range between 0.57 and 0.73. The M2 site contained only Al. The KD values, and published results for intracrystal-line partitioning in epidote and piemontite, show that the preference of Cr3+ for M1 is stronger than that of Fe3+ and Mn3+ in spite of the fact that most Cr3+ is partitioned into M3. Unit-cell parameters of clinozoisite increase with increasing Cr3+. Variations in macroscopic unit-cell parameters can be related to variations in the local M3-Oi and M1-Oi distances.

Key Words: Clinozoisite • zoisite • chromium • synthesis • crystal chemistry • Rietveld refinement







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