Phase changes of CO2 hydrate under high pressure and low temperature

被引:44
|
作者
Hirai, Hisako [1 ]
Komatsu, Kazuki [2 ]
Honda, Mizuho [1 ]
Kawamura, Taro [3 ]
Yamamoto, Yoshitaka [3 ]
Yagi, Takehiko [4 ]
机构
[1] Ehime Univ, Geodynam Res Ctr, Matsuyama, Ehime 7908577, Japan
[2] Univ Tokyo, Geochem Res Ctr, Bunkyo Ku, Tokyo 1130033, Japan
[3] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058569, Japan
[4] Univ Tokyo, Inst Solid State Phys, Chiba 2778581, Japan
来源
JOURNAL OF CHEMICAL PHYSICS | 2010年 / 133卷 / 12期
关键词
CARBON-DIOXIDE CLATHRATE; METHANE HYDRATE; 40; GPA; HYDROGEN; SYSTEM; EQUILIBRIUM;
D O I
10.1063/1.3493452
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
High pressure and low temperature experiments with CO2 hydrate were performed using diamond anvil cells and a helium-refrigeration cryostat in the pressure and temperature range of 0.2-3.0 GPa and 280-80 K, respectively. In situ x-ray diffractometry revealed that the phase boundary between CO2 hydrate and water+CO2 extended below the 280 K reported previously, toward a higher pressure and low temperature region. The results also showed the existence of a new high pressure phase above approximately 0.6 GPa and below 1.0 GPa at which the hydrate decomposed to dry ice and ice VI. In addition, in the lower temperature region of structure I, a small and abrupt lattice expansion was observed at approximately 210 K with decreasing temperature under fixed pressures. The expansion was accompanied by a release of water content from the sI structure as ice Ih, which indicates an increased cage occupancy. A similar lattice expansion was also described in another clathrate, SiO2 clathrate, under high pressure. Such expansion with increasing cage occupancy might be a common manner to stabilize the clathrate structures under high pressure and low temperature. (C) 2010 American Institute of Physics. [doi: 10.1063/1.3493452]
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页数:4
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