High-pressure displacive phase transition of a natural Mg-rich pigeonite (Articolo in rivista)

Type
Label
  • High-pressure displacive phase transition of a natural Mg-rich pigeonite (Articolo in rivista) (literal)
Anno
  • 2011-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1007/s00269-010-0411-2 (literal)
Alternative label
  • Alvaro, M. [ 1 ] ; Nestola, F. [ 2,3 ] ; Camara, F. [ 4 ] ; Domeneghetti, M. C. [ 1 ] ; Tazzoli, V. [ 1 ] (2011)
    High-pressure displacive phase transition of a natural Mg-rich pigeonite
    in Physics and chemistry of minerals
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Alvaro, M. [ 1 ] ; Nestola, F. [ 2,3 ] ; Camara, F. [ 4 ] ; Domeneghetti, M. C. [ 1 ] ; Tazzoli, V. [ 1 ] (literal)
Pagina inizio
  • 379 (literal)
Pagina fine
  • 385 (literal)
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  • ID_PUMA : cnr.igg/2011-A0-082 (literal)
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  • 38 (literal)
Rivista
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  • 5 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • [ 1 ] Univ Pavia, Dipartimento Sci Terra, I-27100 Pavia, Italy [ 2 ] Univ Padua, Dipartimento Geosci, I-35137 Padua, Italy [ 3 ] Univ Padua, Ist Geosci & Georisorse, CNR, I-35137 Padua, Italy [ 4 ] Dipartimento Sci Mineral & Petrrol, I-10125 Turin, Italy (literal)
Titolo
  • High-pressure displacive phase transition of a natural Mg-rich pigeonite (literal)
Abstract
  • A high-pressure single-crystal X-ray diffraction study has been carried out on a P2(1)/c natural Mg-rich pigeonite sample with composition ca. Wo(6)En(76)Fs(18) using a diamond anvil-cell. The unit-cell parameters were determined at 14 different pressures to 7.14 GPa. The sudden disappearance of the b-type reflections (h + k = odd) and a strong discontinuity (about 2.8%) in the unit-cell volume indicated a first-order P2(1)/c-C2/c phase transition between 4.66 and 4.88 GPa. The P(V) data of the P2(1)/c phase were fitted to 4.66 GPa by a third-order Birch-Murnaghan equation of state (BM3 EoS), whereas the limited number of experimental data collected within the C2/c phase between 4.88 and 7.14 GPa were fitted using the same equation of state but with K' constrained to the value obtained for the P2(1)/c fitting. The equation of state coefficients are V (0) = 424.66(6) (3), K (T0) = 104(2) GPa and K' = 8(1) for the P2(1)/c phase, and V (0) = 423.6(1) (3), K (T0) = 112.4(8) GPa, and K' fixed to 8(1) for the C2/c phase. The axial moduli for a, b, and c for the P2(1)/c phase were obtained using also a BM3-EoS, while for the C2/c phase only a linear calculation could be performed, and therefore the same approach was applied for comparison also to the P2(1)/c phase. In general the C2/c phase exhibits axial compressibilities (beta (c) > beta (a) >> beta (b)) lower than those of the P2(1)/c phase (beta (b) > beta (c) a parts per thousand beta (a); similar to those found in previous studies in clinopyroxenes and orthopyroxenes). The lower compressibility of the C2/c phase compared with that of the P2(1)/c could be ascribed to the greater stiffness along the b direction. A previously published relationship between P (c) and M2 average cation radius (i.r.) has been updated using all the literature data on P2(1)/c clinopyroxene containing large cations at M2 site and our new data. The following weighted regression was obtained: P (c) (GPa) = 26(4) - 28(5) x < M2 > i.r (), R (2) = 0.97. This improved equation can be used to predict the critical pressure of natural P2(1)/c clinopyroxene samples just knowing the composition at M2 site. (literal)
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