A high-pressure Raman spectroscopic study of hafnon, HfSiO4
β Scribed by Manoun, B.; Downs, R. T.; Saxena, S. K.
- Book ID
- 121208561
- Publisher
- Mineralogical Society of America
- Year
- 2006
- Tongue
- English
- Weight
- 310 KB
- Volume
- 91
- Category
- Article
- ISSN
- 0003-004X
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β¦ Synopsis
Raman spectra of synthetic HfSiO 4 were determined to pressures of 38.2 GPa. Changes in the spectra indicate that HfSiO 4 undergoes a room-temperature phase transition from the hafnon structure (I4 1 /amd space group) to the scheelite structure (I4 1 /a space group) at a pressure of ~19.6 GPa. Upon release of pressure to ambient conditions, the spectra indicate that the sample retains the scheelite structure. Zircon has been classiΓ ed previously as the least compressible tetrahedrally coordinated silicate known. However, pressure derivatives of the peak positions in hafnon are smaller than those in zircon, and suggest that hafnon is more incompressible than zircon. Furthermore, the pressure derivatives also suggest that the high-pressure, scheelite-structured HfSiO 4 phase is more incompressible than the scheelite-structured ZrSiO 4 (reidite). Thus, the post-hafnon phase appears to be even more incompressible than hafnon, which would make it the least compressible tetrahedrally coordinated silicate known to date.
π SIMILAR VOLUMES
An in situ Raman spectroscopic study was conducted to investigate the pressure-induced phase transformation in the synthetic ZnCr 2 O 4 spinel up to pressures of 70 GPa at room temperature. Results indicate that ZnCr 2 O 4 spinel starts to transform to the CaFe 2 O 4 (or CaTi 2 O 4 ) structure at 17