American Mineralogist; April 2008; v. 93; no. 4;
p. 548-557; DOI: 10.2138/am.2008.2680
© 2008 Mineralogical Society of America
Low-temperature calorimetric and magnetic data for natural end-members of the axinite group
Jan Filip1,2,*,
Edgar Dachs3,
Ji
í Tu
ek1,4,
Milan Novák2 and
Petr Bezdi
ka5
1 Centre for Nanomaterial Research, Palack
University in Olomouc, Svobody 26, 771 46 Olomouc, Czech Republic
2 Department of Geological Sciences, Masaryk University, Kotlá
ská 2, 611 37 Brno, Czech Republic
3 Department of Material Engineering and Physics, University of Salzburg, Hellbrunnerstrasse 34, 5020 Salzburg, Austria
4 Department of Experimental Physics, Palack
University in Olomouc, Svobody 26, 771 46 Olomouc, Czech Republic
5 Institute of Inorganic Chemistry, Academy of Science of the Czech Republic, 250 68
e
, Czech Republic

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FIGURE 1. Chemical compositions of axinite-group minerals. Symbols represent electron microprobe analyses on crystals selected for this study.
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FIGURE 2. Room-temperature 57Fe Mössbauer spectra of axinite-group minerals (except Fe-free magnesioaxinite). Note, both Fe2+ and Fe3+ are in a high-spin state.
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FIGURE 3. Temperature dependence of the heat capacity of axinite-group minerals. Low-temperature regions in the range 0–12 K are inserted. (a) Data for end-member ferroaxinite and magnesioaxinite. (b) Data for manganaxinite and tinzenite.
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FIGURE 4. Heat capacity of ferroaxinite, manganaxinite, and tinzenite in the low-temperature region 0–15 K and functions used to extrapolate CP to 0 K. For manganaxinite and tinzenite, this extrapolation is done in the temperature range 0–5 K on the basis of a Schottky anomaly (solid curves, representing CP lattice + CP Schottky); for ferroaxinite, a lambda-type CP anomaly between 0 and 2 K with a peak at around 1 K was assumed as indicated by the stippled curve.
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Copyright © 2008 by Mineralogical Society of America