Elastic behavior, phase transition, and pressure induced structural evolution of analcime

Elastic and structural behavior of a natural cubic analcime (space group: Ia(3) over bard) from Sardinia (Italy) was investigated at high pressure by in situ single-crystal X-ray diffraction. A first-order phase transition is observed in the pressure range between 0.91(5) and 1.08(5) GPa. Unit-cell constants and reflection conditions confirm that the space group of the HP-polymorph is P(1) over bar. No further phase-transition has been observed at least up to 7.14 GPa. Fitting the volume data of the cubic polymorph with a second-order BM-EoS we obtain: V-0 = 2571.2(4) angstrom(3), K-T0 = 56(3) GPa, and K = 4 (fixed). For the triclinic polymorph, a third-order EoS gives: V-0 = 2607(9) angstrom(3), K-T0 = 19(2) GPa, and K' = 6.8(7). Axial bulk moduli of the triclinic polymorph, calculated with a linearized BM-EoS, are: K-T0(a) = 29(2) GPa, with K'(a) = 4.9(6) and a(0) = 13.727(10) angstrom; K-T0(b) = 20(1) GPa, with K'(b) = 5.2(5), and b(0) = 13.751(15) angstrom; K-T0(c) = 11(1) GPa, with K'(c) = 12.6(6) and c(0) = 13.822(31) angstrom. The elastic behavior of the HP-polymorph appears to be strongly anisotropic, being K-T0(a):K-T0(b):K-T0(c) = 2.64:1.82:1.00. The relevant structural variations in response to the cubic --> triclinic phase transition are due to tetrahedral tilting. The tetrahedral framework distortion gives rise to a change of the eight- and six-ring channels ellipticity and of the extra-framework topological configuration: it appears in fact that for the high-pressure triclinic polymorph the coordination number of some of the Na atoms is seven (2H(2)O + five framework O atoms) instead of six (2H(2)O + four framework O atoms).