期刊
JOURNAL OF MINERALOGICAL AND PETROLOGICAL SCIENCES
卷 99, 期 3, 页码 118-129出版社
JAPAN ASSOC MINERALOGICAL SCIENCES
DOI: 10.2465/jmps.99.118
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High-pressure single crystal X-ray diffraction studies of a natural chondrodite, Mg4.76Fe0.22Ti0.02Si1.99O8' (OH1.26F0.74), and a synthetic OH-chondrodite, Mg4.98Si2.01H2.00O10, were performed using a diamond anvil cell (DAC) up to 7.3 and 5.9 GPa, respectively and at room temperature. FT-IR spectra of the natural chondrodite under high-pressure conditions up to 9.9 GPa was also observed using a DAC. The axial linear compressibilities of these samples are calculated as beta(a) = 1.69(4) x 10(-3), beta(b) = 2.98(4) x 10(-3) and beta(c) = 2.74(5) x 10(-3) (GPa(-1)) for the natural chondrodite and beta(a) = 2.11(18) x 10(-3), beta(b) = 2.83(18) x 10(-3) and beta(c) = 3.04(38) x 10(-3) (GPa(-1)) for the synthetic OH-chondrodite. The isothermal bulk moduli of these samples were calculated as K-Upsilon = 124.1(4) GPa for the natural chondrodite and K-T = 117(2) GPa for the OH-chondrodite, by using the Birch-Murnaghan equation of state assuming K' = 4. The bulk moduli of total void space in each sample, assuming K' = 4, were calculated to be K-square = 116(2) GPa for the natural chondrodite and K-square = 113(4) GPa for the OH-chondrodite. The plots of bulk modulus versus the summation of the filling-factor of polyhedral sites show a good correlation between the humite minerals. This relationship can be explained by the replacement of 4O(2-) + Si4+ double left right arrow 4(F, OH)(-) + square generated in the humite homologous series. In the FT-IR spectra of the natural chondrodite, four OH-stretching vibrational peaks were observed at 3688, 3566, 3558 and 3383 cm(-1) under ambient conditions. The pressure dependences of the frequency of these peaks up to 9.9 GPa are 2.8(3), 3.9(3), 4.0(3) and -2.1(2) (cm(-1)GPa(-1)), respectively. With increasing pressure up to 9.9 GPa, the 3383 cm-1 peak shifts to lower-frequency positions, whereas the other peaks shift to higher-frequency positions. The shortening of the O5 center dot center dot center dot O5 distance, which is not the shared edge between M3 octahedra, related to hydrogen bonding with increasing pressure causes the negative pressure-dependence of the 3383 cm(-1) peak. The positive pressure-dependence of the remaining IR-peaks due to the compression of the O5-H bond, and not related to hydrogen bonding with increasing pressure.
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