JpGU-AGU Joint Meeting 2020

講演情報

[J] 口頭発表

セッション記号 M (領域外・複数領域) » M-IS ジョイント

[M-IS32] ガスハイドレートと地球環境・資源科学

コンビーナ:戸丸 仁(千葉大学理学部地球科学科)、八久保 晶弘(北見工業大学)、後藤 秀作(産業技術総合研究所地圏資源環境研究部門)、谷 篤史(神戸大学 大学院人間発達環境学研究科 人間環境学専攻)

[MIS32-12] メタン+プロパン混合ガスハイドレートの分解挙動観察

*竹谷 敏1鎌田 諒也2八久保 晶弘2 (1.産業技術総合研究所、2.北見工業大学)

キーワード:クラスレートハイドレート、自己保存、天然ガスハイドレート、ホスト-ゲスト相互作用

The existence of enhanced preservation phenomena for structure I methane (CH4) hydrate in the temperature region below ice point (273 K) is one remaining puzzle. This phenomenon has been termed “self-preservation” of gas hydrate. So far, this phenomenon has been observed for CH4 hydrate upon dissociation by rapid pressure-release from high pressures at which CH4 hydrate is stable (Stern et al., 2001). It is also reported that reduction of dissociation rates of gas hydrates by temperature ramping depends on neither the thermodynamic stability nor the crystal structure, but the nature of the guest molecules (Takeya & Ripmeester, 2008). The reduction of dissociation rates of gas hydrates was observed for gas hydrates such as oxygen hydrate, argon hydrate and carbon dioxide hydrate as well as CH4 hydrate. However, the rate reduction was not observed for ethane (C2H6) hydrate, propane (C3H8) hydrate, and mixed gas hydrates of CH4 and C2H6 (Takeya & Ripmeester, 2010).

In this study, powder X-ray diffraction (PXRD) studies of structure II mixed gas hydrates of CH4 and C3H8 as guest with different compositions were performed. Kinetic stability of these mixed gas hydrate was examined by temperature ramping method by means of PXRD. It was revealed that none of them do not show of reduction of dissociation rates. These results may be useful for further understanding of natural gas hydrates.

References
Stern, L. A., Circone, S., Kirby, S. H., Durham, W. B., J. Phys. Chem. B., 2001, 105, 1756.
Takeya, S., Ripmeester, J.A., Angew. Chem. Int. Ed., 2008, 47, 1276.
Takeya, S., Ripmeester, J.A., ChemPhysChem, 2010, 11, 70.