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填充冰 Ih 甲烷水合物在低温高压下的相变化。

Phase changes of filled ice Ih methane hydrate under low temperature and high pressure.

机构信息

Geodynamics Research Center, Ehime University, Matsuyama, Ehime 790-8577, Japan.

出版信息

J Chem Phys. 2013 Sep 14;139(10):104701. doi: 10.1063/1.4820358.

DOI:10.1063/1.4820358
PMID:24050356
Abstract

Low-temperature and high-pressure experiments were performed with filled ice Ih structure of methane hydrate under 2.0-77.0 GPa and 30-300 K using diamond anvil cells and a helium-refrigeration cryostat. In situ X-ray diffractometry revealed distinct changes in the compressibility of the axial ratios of the host framework with pressure. Raman spectroscopy showed a split in the C-H vibration modes of the guest methane molecules, which was previously explained by the orientational ordering of the guest molecules. The pressure and temperature conditions at the split of the vibration modes agreed well with those of the compressibility change. The results indicate the following: (i) the orientational ordering of the guest methane molecules from an orientationally disordered state occurred at high pressures and low temperatures; and (ii) this guest ordering led to anisotropic contraction in the host framework. Such guest orientational ordering and subsequent anisotropic contraction of the host framework were similar to that reported previously for filled ice Ic hydrogen hydrate. Since phases with different guest-ordering manners were regarded as different phases, existing regions of the guest disordered-phase and the guest ordered-phase were roughly estimated by the X-ray study. In addition, above the pressure of the guest-ordered phase, another high-pressure phase developed in the low-temperature region. The deuterated-water host samples were also examined, and the influence of isotopic effects on guest ordering and phase transformation was observed.

摘要

采用金刚石压腔和氦制冷低温恒温器,在 2.0-77.0 GPa 和 30-300 K 的条件下,对甲烷水合物的填充冰 Ih 结构进行了低温高压实验。原位 X 射线衍射表明,随着压力的增加,主体框架的纵横比压缩率发生了明显变化。拉曼光谱显示了客体甲烷分子的 C-H 振动模式的分裂,这以前被解释为客体分子的取向有序。振动模式分裂的压力和温度条件与压缩率变化的条件非常吻合。结果表明:(i)客体甲烷分子从无序取向状态到有序取向状态的取向有序发生在高压和低温条件下;(ii)这种客体有序导致主体框架的各向异性收缩。这种客体取向有序和随后的主体框架各向异性收缩与先前报道的填充冰 Ic 氢水合物相似。由于具有不同客体有序方式的相被认为是不同的相,因此通过 X 射线研究大致估计了客体无序相和客体有序相的存在区域。此外,在客体有序相的压力以上,在低温区域又形成了另一个高压相。还对氘化水主体样品进行了检查,并观察了同位素效应对客体有序和相变的影响。

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