Phase transition induced by solid solution: The BCa- BMg substitution in richteritic amphiboles

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Gianluca Iezzi
  • Giancarlo Della Ventura
  • Mario Tribaudino
  • Peter Nemeth
  • Irene Margiolaki
  • Andrea Cavallo
  • Fabrice Gaillard
  • Harald Behrens

Organisationseinheiten

Externe Organisationen

  • University of Chieti
  • Istituto Nazionale Di Geofisica E Vulcanologia, Rome
  • Universität Rom III
  • University of Parma
  • Hungarian Academy of Sciences
  • European Synchrotron Radiation Facility
  • Universite d'Orleans
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Details

OriginalspracheEnglisch
Seiten (von - bis)369-381
Seitenumfang13
FachzeitschriftAmerican mineralogist
Jahrgang95
Ausgabenummer2-3
PublikationsstatusVeröffentlicht - 1 Feb. 2010

Abstract

Eleven compositions along the join Na(NaMg)Mg5Si 8O22(OH)2Na(NaCa)Mg5Si 8O22(OH)2 ("magnesiorichterite"- richterite) have been synthesized at T = 800-850 °C and PH2O = 0.35-0.5 GPa. The run products have been characterized by electron probe microanalysis (EPMA), synchrotron and conventional X-ray powder diffraction (XRPD), Fourier transformed infrared (FTIR) spectroscopy, and selected area electron diffraction (SAED-TEM). Nominally, the chemical variation along the join can be expressed as BMgxBCa-1xwith 0 ≤ x ≤ 1. A combination of EPMA and FTIR data in the OH-stretching region show that a complete solid solution is obtained under the conditions used. Nev-ertheless, a slight deviation from the nominal compositions involving a limited loss of Na at A and B sites, balanced by an increase of Ca at the B site, is present. Several indications of a displacive and coelastic P21/m → C2/m transformation induced by the Ca-Mg chemical substitution are observed. The phase transition occurs at B-site composition (Xc) close to B(Na1Mg0.7Ca0.3). C2/m samples with a Ca content of 0.34, 0.45, and 0.54 apfu show a significant strain tail related to local compositional inhomogeneities. This residual strain disappears as the amount of BCa significantly increases with respect to that of BMg. The transformation behavior observed here mirrors that of pyroxenes along the join diopside (CaMgSi2O6)-enstatite (Mg2Si 2O6). The cell parameters of amphiboles with CMg5, TSi8, and W(OH)2 and variable A- and B-site populations follow almost linear and continuous trends, indicative of small amounts of spontaneous strain accompanying these monoclinic phase transitions and the absence of significant miscibility gaps among different amphibole groups when quenched from higher temperatures of crystallization.

ASJC Scopus Sachgebiete

Zitieren

Phase transition induced by solid solution: The BCa- BMg substitution in richteritic amphiboles. / Iezzi, Gianluca; Ventura, Giancarlo Della; Tribaudino, Mario et al.
in: American mineralogist, Jahrgang 95, Nr. 2-3, 01.02.2010, S. 369-381.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Iezzi, G, Ventura, GD, Tribaudino, M, Nemeth, P, Margiolaki, I, Cavallo, A, Gaillard, F & Behrens, H 2010, 'Phase transition induced by solid solution: The BCa- BMg substitution in richteritic amphiboles', American mineralogist, Jg. 95, Nr. 2-3, S. 369-381. https://doi.org/10.2138/am.2010.3308
Iezzi, G., Ventura, G. D., Tribaudino, M., Nemeth, P., Margiolaki, I., Cavallo, A., Gaillard, F., & Behrens, H. (2010). Phase transition induced by solid solution: The BCa- BMg substitution in richteritic amphiboles. American mineralogist, 95(2-3), 369-381. https://doi.org/10.2138/am.2010.3308
Iezzi G, Ventura GD, Tribaudino M, Nemeth P, Margiolaki I, Cavallo A et al. Phase transition induced by solid solution: The BCa- BMg substitution in richteritic amphiboles. American mineralogist. 2010 Feb 1;95(2-3):369-381. doi: 10.2138/am.2010.3308
Iezzi, Gianluca ; Ventura, Giancarlo Della ; Tribaudino, Mario et al. / Phase transition induced by solid solution : The BCa- BMg substitution in richteritic amphiboles. in: American mineralogist. 2010 ; Jahrgang 95, Nr. 2-3. S. 369-381.
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abstract = "Eleven compositions along the join Na(NaMg)Mg5Si 8O22(OH)2Na(NaCa)Mg5Si 8O22(OH)2 ({"}magnesiorichterite{"}- richterite) have been synthesized at T = 800-850 °C and PH2O = 0.35-0.5 GPa. The run products have been characterized by electron probe microanalysis (EPMA), synchrotron and conventional X-ray powder diffraction (XRPD), Fourier transformed infrared (FTIR) spectroscopy, and selected area electron diffraction (SAED-TEM). Nominally, the chemical variation along the join can be expressed as BMgxBCa-1xwith 0 ≤ x ≤ 1. A combination of EPMA and FTIR data in the OH-stretching region show that a complete solid solution is obtained under the conditions used. Nev-ertheless, a slight deviation from the nominal compositions involving a limited loss of Na at A and B sites, balanced by an increase of Ca at the B site, is present. Several indications of a displacive and coelastic P21/m → C2/m transformation induced by the Ca-Mg chemical substitution are observed. The phase transition occurs at B-site composition (Xc) close to B(Na1Mg0.7Ca0.3). C2/m samples with a Ca content of 0.34, 0.45, and 0.54 apfu show a significant strain tail related to local compositional inhomogeneities. This residual strain disappears as the amount of BCa significantly increases with respect to that of BMg. The transformation behavior observed here mirrors that of pyroxenes along the join diopside (CaMgSi2O6)-enstatite (Mg2Si 2O6). The cell parameters of amphiboles with CMg5, TSi8, and W(OH)2 and variable A- and B-site populations follow almost linear and continuous trends, indicative of small amounts of spontaneous strain accompanying these monoclinic phase transitions and the absence of significant miscibility gaps among different amphibole groups when quenched from higher temperatures of crystallization.",
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TY - JOUR

T1 - Phase transition induced by solid solution

T2 - The BCa- BMg substitution in richteritic amphiboles

AU - Iezzi, Gianluca

AU - Ventura, Giancarlo Della

AU - Tribaudino, Mario

AU - Nemeth, Peter

AU - Margiolaki, Irene

AU - Cavallo, Andrea

AU - Gaillard, Fabrice

AU - Behrens, Harald

PY - 2010/2/1

Y1 - 2010/2/1

N2 - Eleven compositions along the join Na(NaMg)Mg5Si 8O22(OH)2Na(NaCa)Mg5Si 8O22(OH)2 ("magnesiorichterite"- richterite) have been synthesized at T = 800-850 °C and PH2O = 0.35-0.5 GPa. The run products have been characterized by electron probe microanalysis (EPMA), synchrotron and conventional X-ray powder diffraction (XRPD), Fourier transformed infrared (FTIR) spectroscopy, and selected area electron diffraction (SAED-TEM). Nominally, the chemical variation along the join can be expressed as BMgxBCa-1xwith 0 ≤ x ≤ 1. A combination of EPMA and FTIR data in the OH-stretching region show that a complete solid solution is obtained under the conditions used. Nev-ertheless, a slight deviation from the nominal compositions involving a limited loss of Na at A and B sites, balanced by an increase of Ca at the B site, is present. Several indications of a displacive and coelastic P21/m → C2/m transformation induced by the Ca-Mg chemical substitution are observed. The phase transition occurs at B-site composition (Xc) close to B(Na1Mg0.7Ca0.3). C2/m samples with a Ca content of 0.34, 0.45, and 0.54 apfu show a significant strain tail related to local compositional inhomogeneities. This residual strain disappears as the amount of BCa significantly increases with respect to that of BMg. The transformation behavior observed here mirrors that of pyroxenes along the join diopside (CaMgSi2O6)-enstatite (Mg2Si 2O6). The cell parameters of amphiboles with CMg5, TSi8, and W(OH)2 and variable A- and B-site populations follow almost linear and continuous trends, indicative of small amounts of spontaneous strain accompanying these monoclinic phase transitions and the absence of significant miscibility gaps among different amphibole groups when quenched from higher temperatures of crystallization.

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