Title
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Mössbauer effect study of anapaite, , and of its oxidation products
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Author
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Abstract
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Mossbauer spectra (MS) of anapaite (Ca-2 Fe2+ (PO4)(2) . 4H(2)O) and of a sample after being immersed in a 4% H2O2 solution at room temperature (RT) over 12 days (hereafter an4ox) were collected at temperatures in the range 4.2 to 420 K and 11 to 300 K respectively. All MS consist of symmetrical doublets. hence magnetic ordering was not observed. The Fe2+ centre shifts of temperature dependencies of the Fe2+ centre shifts of anapaite and an4ox were analysed with the Debye model for the lattice vibrations. The characteristic Mossbauer temperatures were found as 370 K +/- 25 K and 340 K +/- 25 It. and the intrinsic isomer shifts as 1.427 +/- 0.005 mm/s and 1.418 +/- 0.005 mm/s respectively. From the external-field (60 kOe) MS recorded at 4.2 and 189 K for the non-treated sample, the principal component V-zz of the electric field gradient (EFG) is determined to be positive and the asymmetry parameter eta approximate to 0.2 and 0.4 respectively. The temperature variations of the quadrupole splittings, Delta E-Q(T), cannot be interpreted on the basis of the thermal population of the D-5 electronic levels resulting from the tetragonal compression of the O-6 co-ordination. The low-temperature linear behaviour of Delta E-Q(T) is attributed to a strong orbit-lattice coupling. A field of 60 kOe applied to anapaite at 4.2 K produces magnetic hyperfine splitting with effective hyperfine fields of -136. -254 and -171 kOe along the principal axes Ox, Oy and Oz of the EFG tensor respectively. Additional oxidation treatments in solutions with various H2O2 concentrations up to 20% and subsequent Mossbauer experiments at room temperature, have revealed that the anapaite structure is not sensitive to oxidation since eventually only a small amount of Fe2+ (similar to 6.5%) is converted into Fe3+. |
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Language
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English
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Source (journal)
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Physics and chemistry of minerals. - Berlin
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Publication
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Berlin
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1999
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ISSN
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0342-1791
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DOI
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10.1007/S002690050213
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Volume/pages
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26
:6
(1999)
, p. 506-512
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ISI
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000081850100011
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Full text (Publisher's DOI)
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Full text (publisher's version - intranet only)
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