MRI observation of CO2-C3H8 hydrate-induced water migration in glass sand

被引:17
|
作者
Zheng, Jia-nan [1 ]
Jiang, Lanlan [1 ]
Wang, Pengfei [1 ]
Zhou, Hang [1 ]
Yang, Mingjun [1 ]
机构
[1] Dalian Univ Technol, Minist Educ, Key Lab Ocean Energy Utilizat & Energy Conservat, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
Gas hydrate; Water migration; Carbon dioxide; Propane; CARBON-DIOXIDE; PHASE-EQUILIBRIUM; POROUS-MEDIA; GAS-MIXTURES; FLUE-GAS; CAPTURE; CO2; SEPARATION; HYDROGEN; PROPANE;
D O I
10.1016/j.ces.2019.07.038
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Hydrate-induced water migration is an unusual behaviour that occurs in certain hydrate formation processes, such as in the formation of propane-containing hydrate. This study is the first to investigate the continuous, staged processes of constant-volume formation, constant-pressure reformation and exhaust dissociation of CO2-C3H8 hydrates using the magnetic resonance imaging (MRI) technique. Real-time MRI images indicate that the formation of CO2-C3H8 hydrates draw water from its surroundings, causing the local water saturation to increase. As the concentrated water can further form hydrates and extend to the gas phase, the water appears as though it climbs upward through the glass sand and hydrate zone towards the gas phase. Experiments under different formation pressures indicate that the locations of hydrate-induced water migration are uncertain and depend on hydrate nucleation. The evolution processes of hydrate-induced water migration under different initial pressures have good similarity. In addition, water migration will still occur during the reformation stage. The initial pressure has great effects on both the formation and dissociation of hydrate. In addition, faster dissociation may make the water move upward due to strong gas release. The findings in this study are significant to future research on propane-containing hydrate, especially for hydrate-based seawater desalination applications. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1096 / 1106
页数:11
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