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

Mineralogical Magazine; December 2000; v. 64; no. 6; p. 983-993
© 2000 Mineralogical Society of Great Britain and Ireland
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
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pavese, A.
Right arrow Articles by Ivaldi, G.
Right arrow Search for Related Content
GeoRef
Right arrow GeoRef Citation

In situ high temperature single crystal X-ray diffraction study of a natural omphacite

A. Pavese1,2,*, R. Bocchio3 and G. Ivaldi4

1 Dipartimento Scienze della Terra-Università degli Studi di Milano, Via Botticelli 23, 20133 Milano, Italy
2 National Research Council, Centro di Studio per la geodinamica alpina e quaternaria, Via Botticelli 23, 20133 Milano, Italy
3 Dipartimento Scienze della Terra-Università degli Studi di Milano, Via Botticelli 23, 20133 Milano, Italy
4 Dipartimento Scienze Mineralogiche e Petrologiche-Università degli Studi di Torino, Via Valperga Caluso 35, 10125 Torino, Italy

* E-mail: pavese{at}p8000.terra.unimi.it

In situ high temperature single crystal X-ray diffraction (XRD) experiments have been performed on a chemically quasi-ideal omphacite sample [(Ca0.49Na0.51){sum}1(Mg0.46Al0.48Fe0.063+){sum}1(Si1.97Al0.03){sum}2O6], up to 1000°C. The lattice parameters were studied as a function of temperature, and their thermal expansion coefficients determined. The b and c cell edges show discontinuities as a function of temperature which are interpreted here in terms of intracrystalline cation diffusion processes. Structure refinements have been carried out using data collected at room temperature, at 800°C and at ambient conditions after cooling. The structural behaviour as a function of temperature of chemically quasi-ideal omphacites is compared with those of jadeite and diopside.

KEYWORDS: omphacites, high temperature, thermal expansion




This article has been cited by other articles:


Home page
Can MineralHome page
R. Bocchio, L. De Capitani, and L. Ottolini
NEW CHEMICAL DATA ON THE CLINOPYROXENE-GARNET PAIR IN THE ALPE ARAMI ECLOGITE, CENTRAL ALPS, SWITZERLAND
Can Mineral, August 1, 2004; 42(4): 1205 - 1219.
[Abstract] [Full Text] [PDF]


Home page
American MineralogistHome page
Y. Nishihara, Y. Nishihara, E. Takahashi, K. Matsukage, and T. Kikegawa
Thermal equation of state of omphacite
American Mineralogist, January 1, 2003; 88(1): 80 - 86.
[Abstract] [Full Text] [PDF]




JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2008 by Mineralogical Society of Great Britain and Ireland