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1 School of Earth, Atmospheric and Environmental Sciences, University of Manchester, Manchester, M13 9PL, U.K.
2 Daresbury Laboratory, Daresbury, Cheshire WA4 4AD, U.K.
3 Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, California 94720, U.S.A.
Correspondence:
E-mail: alison.pawley{at}manchester.ac.uk
The effects of pressure on the OH stretching frequencies of natural talc and two samples of synthetic 10-Å phase have been measured using a diamond-anvil cell and a synchrotron infrared source. The 10-Å phase was synthesized at 6.06.5 GPa, 600 °C for 46 hours (sample 10Å-46) and 160 hours (10Å-160). Spectra were collected up to 9.0 GPa (talc), 9.9 GPa (10Å-46), and 9.6 GPa (10Å-160). The OH stretching vibration of Mg3OH groups in talc occurs at 3677 cm1 at ambient pressure, and increases linearly with pressure at 0.97(2) cm1 GPa1. The same vibration occurs in 10-Å phase, but shows negligible pressure shift up to 2 GPa, above which the frequency increases linearly to the maximum pressure studied, at a rate of 0.96(3) cm1 GPa1 (10Å-46) and 0.87(3) cm1 GPa1 (10Å-160). Two other prominent bands in the 10-Å phase spectrum are suggested to be due to stretching of interlayer H2O, hydrogen-bonded to the nearest tetrahedral sheet. These bands also show little change over the first 2 GPa of compression, as most of the compression of the structure is taken up by closing non-hydrogen bonded gaps between interlayer H2O and tetrahedral sheets. Between 2 and 4 GPa, changes in band intensities suggest a rearrangement of the interlayer H2O.
Key Words: Talc 10-Å phase high-pressure studies IR spectroscopy
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A.E. Gleason, S.A. Parry, A.R. Pawley, R. Jeanloz, and S.M. Clark Pressure-temperature studies of talc plus water using X-ray diffraction American Mineralogist, July 1, 2008; 93(7): 1043 - 1050. [Abstract] [Full Text] [PDF] |
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