Preferential dissolution of SiO2 from enstatite to H2 fluid under high pressure and temperature.
Preferential dissolution of SiO2 from enstatite to H2 fluid under high pressure and temperature.
复制标题
在高压和高温下,SiO2 从顽辉石中优先溶解到 H2 流体中。
DOI:
10.1007/s00269-015-0792-3
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发表时间:
2015
影响因子:
1.4
通讯作者:
Nakano S. and Yagi T.
中科院分区:
文献类型:
--
作者:
Shinozaki A.;Kagi H.;Hirai H.;Ohfuji H.;Okada T.;Nakano S. and Yagi T.
Stability and phase relations of coexisting enstatite and H2fluid were investigated in the pressure and temperature regions of 3.1–13.9 GPa and 1500–2000 K using laser-heated diamond-anvil cells. XRD measurements showed decomposition of enstatite upon heating to form forsterite, periclase, and coesite/stishovite. In the recovered samples, SiO2grains were found at the margin of the heating hot spot, suggesting that the SiO2component dissolved in the H2fluid during heating, then precipitated when its solubility decreased with decreasing temperature. Raman and infrared spectra of the coexisting fluid phase revealed that SiH4and H2O molecules formed through the reaction between dissolved SiO2and H2. In contrast, forsterite and periclase crystals were found within the hot spot, which were assumed to have replaced the initial orthoenstatite crystals without dissolution. Preferential dissolution of SiO2components of enstatite in H2fluid, as well as that observed in the forsterite H2system and the quartz H2system, implies that H2-rich fluid enhances Mg/Si fractionation between the fluid and solid phases of mantle minerals.