Kurnosov Alexander V, Ogienko Andrey G, Goryainov Sergei V, Larionov Eduard G, Manakov Andrey Y, Lihacheva Anna Y, Aladko Eugeny Y, Zhurko Fridrikh V, Voronin Vladimir I, Berger Ivan F, Ancharov Aleksei I
Nikolaev Institute of Inorganic Chemistry, SB RAS, Akad. Lavrentieva Avenue 3, Novosibirsk 630090, Russian Federation.
J Phys Chem B. 2006 Nov 2;110(43):21788-92. doi: 10.1021/jp0636726.
Dissociation temperatures of gas hydrate formed in the ethane-water system were studied at pressures up to 1500 MPa. In situ neutron diffraction analysis and X-ray diffraction analysis in a diamond anvil cell showed that the gas hydrate formed in the ethane-water system at 340, 700, and 1840 MPa and room temperature belongs to the cubic structure I (CS-I). Raman spectra of C-C vibrations of ethane molecules in the hydrate phase, as well as the spectra of solid and liquid ethane under high-pressure conditions were studied at pressures up to 6900 MPa. Within 170-3600 MPa Raman shift of the C-C vibration mode of ethane in the hydrate phase did not show any discontinuities, which could be evidence of possible phase transformations. The upper pressure boundary of high-pressure hydrate existence was discovered at the pressure of 3600 MPa. This boundary corresponds to decomposition of the hydrate to solid ethane and ice VII. The type of phase diagram of ethane-water system was proposed in the pressure range of hydrate formation (0-3600 MPa).
在高达1500兆帕的压力下,研究了乙烷 - 水体系中形成的气体水合物的分解温度。在金刚石对顶砧池中进行的原位中子衍射分析和X射线衍射分析表明,在340、700和1840兆帕以及室温下,乙烷 - 水体系中形成的气体水合物属于立方结构I(CS - I)。在高达6900兆帕的压力下,研究了水合物相中乙烷分子C - C振动的拉曼光谱以及高压条件下固态和液态乙烷的光谱。在170 - 3600兆帕范围内,水合物相中乙烷的C - C振动模式的拉曼位移没有显示出任何不连续性,这可能是可能发生相变的证据。在3600兆帕的压力下发现了高压水合物存在的压力上限。该边界对应于水合物分解为固态乙烷和冰VII。提出了乙烷 - 水体系在水合物形成压力范围(0 - 3600兆帕)内的相图类型。