Chemical Reactions In The Fe2sio4-D-2 System With A Variable Deuterium Content At 7.5 Gpa

AMERICAN MINERALOGIST(2021)

引用 1|浏览5
暂无评分
摘要
Hydrogen-induced decomposition of fayalite (Fe2SiO4) at high pressure is of considerable interest for a better understanding of the chemical processes occurring in the cores and mantles of icy satellites. At pressures up to 10 GPa and temperatures 250-300 degrees C (typical of the cores and mantles of Jupiter's and Saturn's satellites), a variable amount of hydrogen can react with fayalite contained in their rocks. Volatile compounds that can form via these reactions are usually identified by mass spectroscopy. In our experiments, we used compressed deuterium gas instead of hydrogen to ensure that the volatiles analyzed by mass spectroscopy could only result from the decomposition of fayalite. To study the effect of the amount of deuterium present in the system, the fayalite (Fa) samples were deuterated at P = 7.5 GPa and T = 280 degrees C with the preset molar ratios D-2/Fa = 1, 1.5, 2.2, and 5 in the reaction cell. The deuterated samples were further quenched to the liquid N-2 temperature and, after releasing the pressure, removed from the reaction cell and studied by quadrupole mass-spectroscopy, X-ray diffraction, and Raman spectroscopy. Our results showed that the high-pressure deuteration invariably led to the chemical decomposition of fayalite. The solid products of the reaction varied from a mixture of ferrosilite (FeSiO3) and iron at D-2/Fa = 1 to a mixture of silica and iron at D-2/Fa = 2.2. The decomposition occurred via breaking the Fe-O bonds and was always accompanied by the formation of water. Applying the observed reactions to the natural conditions of, e.g., the center of Titan or Ganymede, one may infer that fayalite can be dissolved in the hydrogen fluid or replaced by iron, ferrosilite, or silica depending on the molar ratio H-2/Fa.
更多
查看译文
关键词
Fayalite, hydrogen, ferrosilite, high pressure, decomposition reaction, silica, iron
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要