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Temperature-dependent Fe2+–Mn2+ order–disorder behaviour in amphiboles |
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| Authors: | J J Reece S A T Redfern M D Welch C M B Henderson C A McCammon |
| Institution: | Department of Earth Sciences, University of Cambridge, Downing Street, Cambridge, CB2 3EQ, UK, E-mail: satr@cam.ac.uk, GB Department of Earth Sciences, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK, GB Bayerisches Geoinstitut, Universit?t Bayreuth, 95440, Bayreuth, Germany, GB |
| Abstract: | The partitioning of Fe and Mn between the large M(4) site and the octahedral sites, M(1,2,3) in the amphibole structure has been investigated in two natural manganogrunerites of compositions Ca0.1Mn1.9 Mg1.25Fe2+ 3.56Fe3+ 0.38Si7.81O22(OH)2 and Ca0.24Mn1.57 Mg2.27 Fe2+ 2.76Fe3+ 0.32Si7.84O22(OH)2. The long-range cation distribution in the two samples has been elucidated by in situ neutron powder diffraction revealing that Mn is preferentially ordered onto M(4) ? M(2) >M(1) >M(3) in both samples. Partitioning of Mn from M(4) into the octahedral sites begins at 350 °C, with site exchange energies of ?16.6 kJ mol?1 and ?14.9 kJ mol?1, in samples containing 1.90 and 1.57 Mn apfu, respectively. Mössbauer and infrared spectroscopy have been used to study the samples at room temperature, and Mössbauer data agree well with the diffraction results, confirming that high-temperature cation distributions are retained during cooling. The fine structure in the hydroxyl-stretching region of the IR absorption spectra has been used to discuss qualitatively the site occupancies of the coordinating M(1)M(3)M(1) triplet, linked by O(3). On the basis of such modelling, we conclude that a degree of local clustering is present in both samples. |
| Keywords: | Cation partitioning Order– disorder Neutron diffraction FTIR and M?ssbauer spectroscopy |
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