Solid solutions and phase transitions in (Ca,M2+)M2+Si2O6 pyroxenes (M2+ = Co, Fe, Mg)

Luciana Mantovani*, Mario Tribaudino, Giovanni Bertoni, Giancarlo Salviati, Geoffrey Bromiley

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

The effect of the substitution of Ca with Co, on the phase transition and on the extension of the the extension of the miscibility gap, was studied to model the general mechanism of phase transitions and solid solutions in (Ca,M2+)M2+Si2O6 pyroxenes. Eleven pyroxenes with composition Ca1-xCo1+xSi2O6, (0

The cell parameters of the Ca-Co pyroxenes undergo a sudden change at the composition of about 0.4 Ca apfu, due to the C2/cP2(1)/c phase transition. The change in volume with composition follows an ideal trend, in the C2/c phase, dictated by the ionic size of the substituting cation. Deviation from the C2/c behavior are instead observed in the P2(1)/c field and ascribed to volume strain. The same turnover was found in Ca-Mg, Ca-Fe, and Ca-Mn pyroxenes. The C2/cP2(1)/c transition occurs with decreasing the M2 average cation radius, down to a critical value between 0.85 and 0.88 angstrom, depending on the series. A stabilization of the C2/c phase related to crystal field in Ca-Fe and Ca-Co pyroxenes is suggested by the analysis of the volume strain in the P2(1)/c field. A key finding is that a miscibility gap may develop either by lattice strain related to cation substitution, within a series where all end-members have the same structure, or for the combined effect of lattice strain and a phase transition, as is the case for pyroxenes.

Original languageEnglish
Pages (from-to)704-711
Number of pages8
JournalAmerican Mineralogist
Issue number4
Publication statusPublished - Apr 2014

Keywords / Materials (for Non-textual outputs)

  • Ca-Co pyroxenes
  • high-pressure synthesis
  • phase transition
  • phase equilibria
  • JOIN
  • C2/C


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