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

American Mineralogist; December 1999; v. 84; no. 11-12; p. 1861-1869
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yanagisawa, K.
Right arrow Articles by Oishi, S.
Right arrow Search for Related Content
GeoRef
Right arrow GeoRef Citation

Topotaxial replacement of chlorapatite by hydroxyapatite during hydrothermal ion exchange

K. Yanagisawa, J. C. Rendon-Angeles, N. Ishizawa, and S. Oishi

Kochi University, Research Laboratory of Hydrothermal Chemistry, Kochi, Japan

Exchange of Cl (super -) by OH (super -) in synthesized chlorapatite single crystals was investigated under hydrothermal conditions. Hydrothermal treatments were performed at various temperatures from 200 to 500 degrees C, for intervals between 3 and 96 h in KOH or NaOH solutions. Ion exchange of Cl (super -) in the chlorapatite crystals was completed at low temperature (500 degrees C) for a short time (12 h) in 6.25 M KOH solution, and resulted in the formation of hydroxyapatite. The rate of ion exchange was accelerated by increasing the reaction temperature and/or concentration of the alkaline solutions. That the converted crystals were single crystals of hydroxyapatite was confirmed by X-ray precession photographs. The hydroxyapatite single crystals that formed from the chlorapatite single crystals by the topotaxial ion exchange under alkaline hydrothermal conditions had a characteristic texture, exhibiting channels on the surfaces and tunnels inside, both along the c axis of the crystals. A dissolution and precipitation process is proposed for the ion-exchange reaction conducted under hydrothermal conditions.

This record provided courtesy of AGI/GeoRef.




This article has been cited by other articles:


Home page
American MineralogistHome page
L. Fernandez-Diaz, C. M. Pina, J. M. Astilleros, and N. Sanchez-Pastor
The carbonatation of gypsum: Pathways and pseudomorph formation
American Mineralogist, August 1, 2009; 94(8-9): 1223 - 1234.
[Abstract] [Full Text] [PDF]


Home page
American MineralogistHome page
D. E. Harlov, R. Wirth, and C. J. Hetherington
The relative stability of monazite and huttonite at 300 900 {degrees}C and 200 1000 MPa: Metasomatism and the propagation of metastable mineral phases
American Mineralogist, October 1, 2007; 92(10): 1652 - 1664.
[Abstract] [Full Text] [PDF]


Home page
American MineralogistHome page
D. E. Harlov, D. E. Harlov, and H.-J. Forster
Fluid-induced nucleation of (Y+REE)-phosphate minerals within apatite: Nature and experiment. Part II. Fluorapatite
American Mineralogist, August 1, 2003; 88(8-9): 1209 - 1229.
[Abstract] [Full Text] [PDF]


Home page
Mineral MagHome page
A. Putnis
Mineral replacement reactions: from macroscopic observations to microscopic mechanisms
Mineralogical Magazine, October 1, 2002; 66(5): 689 - 708.
[Abstract] [Full Text] [PDF]




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