Publications by authors named "Go Fuseya"

Knowledge of carbon isotope fractionation is needed in order to discuss the formation and dissociation of naturally occurring CO hydrates. We investigated carbon isotope fractionation during CO hydrate formation and measured the three-phase equilibria of CO-HO and CO-HO systems. From a crystal structure viewpoint, the difference in the Raman spectra of hydrate-bound CO and CO was revealed, although their unit cell size was similar.

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C-H symmetric stretching vibrational frequencies of CH, CH and CH molecules encapsulated in 5, 56 and 56 cages of structures I (sI) and II (sII) clathrate hydrates measured by Raman spectroscopy in the temperature range of 93-183 K was analysed. The slopes of the symmetric stretch vibrational frequencies under changing temperatures (Δ/Δ) for CH, CH and CH molecules encapsulated in sII 56 cages were smaller than those for molecules in sI 56 cages, although sI 56 cages are smaller than sII 56 cages. We compared the results of Δ/Δ in this study with the geometrical properties of each host water cage, and these comparisons suggest that the geometry of host water cages affects Δ/Δ.

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Large molecules such as 2-methylbutane (CH) or 2,2-dimethylbutane (CH) form structure H (sH) hydrates with methane (CH) as a help gas. In this study, the Raman spectra of the C-H symmetric stretch region of CH enclathrated within various sH hydrates and structure I CH hydrates were analyzed in the temperature range 137.7-205.

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Large molecules such as 2-methylbutane (CH) or 2,2-dimethylbutane (CH) form structure H (sH) hydrates with methane (CH) as a help gas. In this study, the Raman spectra of the C-H symmetric stretch region of CH enclathrated within various sH hydrates and structure I CH hydrates were analyzed in the temperature range 83-183 K. Thermal expansions of these sH hydrate samples were also measured using powder X-ray diffraction.

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