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Hydrogen-carbonate ion in synthetic high-pressure apatite

Michael E. Fleet and Xi Liu
Hydrogen-carbonate ion in synthetic high-pressure apatite
American Mineralogist (October 2007) 92 (10): 1764-1767

Abstract

The hydrogen-carbonate ion [(HCO (sub 3) ) (super -) ] has been detected by Fourier transform infrared (FTIR) spectroscopy in the c-axis structural channel of Na-bearing type A-B carbonate apatite synthesized under conditions of high P (0.1-1 GPa), T (800-1350 degrees C), and p(CO (sub 2) ), and accounts for up to one-third of the total complement of channel carbonate. The hydrogen-carbonate ion is only loosely bound in the apatite channel, and breaks down on aging at room temperature. Volatile decomposition products are lost from the carbonate apatite structure, with CO (sub 2) more mobile than H (sub 2) O. The mobility of small volatile molecules points to a possible role for the apatite channel in mediating acid-base reactions in restricted surficial environments and biological systems.


ISSN: 0003-004X
EISSN: 1945-3027
Coden: AMMIAY
Serial Title: American Mineralogist
Serial Volume: 92
Serial Issue: 10
Title: Hydrogen-carbonate ion in synthetic high-pressure apatite
Affiliation: University of Western Ontario, Department of Earth Sciences, London, ON, Canada
Pages: 1764-1767
Published: 200710
Text Language: English
Publisher: Mineralogical Society of America, Washington, DC, United States
References: 20
Accession Number: 2007-117240
Categories: Mineralogy of non-silicates
Document Type: Serial
Bibliographic Level: Analytic
Illustration Description: illus.
Country of Publication: United States
Secondary Affiliation: GeoRef, Copyright 2017, American Geosciences Institute. Abstract, copyright, Mineralogical Society of America. Reference includes data from GeoScienceWorld, Alexandria, VA, United States
Update Code: 200748
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