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http://hdl.handle.net/2122/4834
Authors: | Iezzi, G.* Liu, Z.* Della Ventura, G.* |
Title: | Synthetic ANaB(NaxLi1 ¡ xMg1)CMg5Si8O22(OH)2 (with x = 0.6, 0.2 and 0) P21/m amphiboles at high pressure: a synchrotron infrared study | Journal: | Physics and Chemistry of Minerals | Series/Report no.: | /36 (2009) | Publisher: | Springer | Issue Date: | 2009 | DOI: | 10.1007/s00269-008-0282-y | Keywords: | High-pressure B-site dimension |
Subject Classification: | 04. Solid Earth::04.01. Earth Interior::04.01.04. Mineral physics and properties of rocks | Abstract: | high-pressure behavior of three synthetic amphiboles crystallized with space group P21/m at room conditions in the system Li2O–Na2O–MgO–SiO2–H2O has been studied by in situ synchrotron infrared absorption spectroscopy. The amphiboles have compositions ANa B(NaxLi1 ¡ xMg1) CMg5 Si8 O22(OH)2 with x = 0.6, 0.2 and 0.0, respectively. The high-P experiments up to 32 GPa were carried out on the U2A beamline at Brookhaven National Laboratory (NY, USA) using a diamond anvil cell under non-hydrostatic or quasi-hydrostatic conditions. The two most intense absorption bands in the OH-stretching infrared spectra can be assigned to two non-equivalent O–H dipoles in the P21/m structure, bonded to the same local environment M1M3Mg3–OH–ANa, and pointing toward two diVerently kinked tetrahedral rings. In all samples these bands progressively merge to give a unique symmetrical absorption with increasing pressure, suggesting a change in symmetry from P21/m to C2/m. The pressure at which the transition occurs appears to be linearly correlated to the aggregate B-site dimension. The infrared spectra collected for amphibole B(Na0.2Li0.8Mg1) in the frequency range 50 to 1,400 cm¡1 also show a series of changes with increasing pressure. The data reported here support the inference of Iezzi et al. (Am Miner 91:479–482, 2006a) regarding a new high-pressure C2/m amphibole polymorph characterized by two equivalent and kinked double-chains, stable at very high-pressure. |
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