- journal_title：American Mineralogist
- Contributor：Fabrizio Nestola ; Tiziana Boffa Ballaran ; Ross J. Angel ; Jing Zhao ; Haruo Ohashi
- Publisher：Mineralogical Society of America
- Date：2010-
- Format：text/html
- Language：en
- Identifier：10.2138/am.2010.3396
- journal_abbrev：American Mineralogist
- issn：0003-004X
- volume：95
- issue：5-6
- firstpage：832
- section：Articles
Two C2/c pyroxenes, CaMnSi2O6 and CaZnSi2O6, were investigated at high pressure by single-crystal X-ray diffraction. Their unit-cell parameters were determined at 9 different pressures up to 7.55 and 8.23 GPa, respectively. No evidence of phase transformations was found for either sample throughout the investigated pressure range. The pressure-volume data were fit using a third-order Birch-Murnaghan equation of state and it was possible to refine simultaneously the unit-cell volume V0, the bulk modulus KT0 and its first pressure derivative K′ providing the following coefficients: V0 = 462.01(3) Å3, KT0 = 97.3(4) GPa, K′ = 7.5(2) for CaMnSi2O6 and V0 = 444.79(2) Å3, KT0 = 109.6(5) GPa, K′ = 7.0(2) for CaZnSi2O6. The substitution of Zn for Mn at the M1 crystallographic site causes a strong decrease of the bulk modulus (by about 11%). Intensity data were collected at several pressures for both samples. The main compression mechanism is related to the tetrahedral chain kinking and the consequent shortening of the Ca-O3long bond distances, which show a markedly larger decrease for the CaMnSi2O6 sample. Comparing the results obtained in this work with previous data for Ca/Na-bearing C2/c pyroxenes containing trivalent and divalent 3d-transition elements at M1 site, we identified two distinct compressibility trends: for a similar unit-cell volume at room pressure the pyroxenes with Na on M2 and trivalent cations on M1 are more compressible than those having Ca on M2 and divalent cations at the M1 site. The analysis of the structure evolution for all samples indicates that this is strongly correlated with the evolution of kinking of the tetrahedral chains and the shortening of the M2-O3 bonds.