宋永臣

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:能源与动力学院

学科:能源与环境工程

办公地点:能动大楼810

联系方式:songyc@dlut.edu.cn

电子邮箱:songyc@dlut.edu.cn

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Direct measurement of pore gas pressure and water/gas phase transitions during methane hydrate dissociation

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论文类型:期刊论文

发表时间:2020-06-01

发表刊物:MARINE AND PETROLEUM GEOLOGY

收录刊物:EI、SCIE

卷号:116

ISSN号:0264-8172

关键字:Hydrate dissociation; Magnetic resonance imaging; MR/MRI-Compatible metallic core holder; Phase evolution; Capillary-trapped residual gas; Elevated pore pressure

摘要:Methane hydrate deposits worldwide are vast potential sources of natural gas. Although field tests, and many laboratory studies, of hydrate dissociation have been performed, long term gas recovery from hydrate deposits still requires a comprehensive knowledge of the pore gas pressure and related phenomena. Pore gas pressure can significantly affect the safety and efficiency of gas production from hydrate deposits. Capillary-trapped residual gas saturation, known to cause elevated pore gas pressure during methane hydrate dissociation, was measured by magnetic resonance. Elevated pore gas pressure was estimated to be 8500 psi. Different molecular species and fluid environments produced during the methane hydrate dissociation process were discriminated. The results show that the majority of gas is initially confined as capillary-trapped gas upon dissociation. The evolution of water and gas saturations was measured as a function of time. Water migration, bed failure, and crack growth, related to elevated pore gas pressure, were observed both spatially and temporally resolved. Hydrate dissociation proceeded from the sand pack exterior to the interior, in a shrinking core manner, due to heat transfer effects. It was observed that hydrate dissociation resulted in pronounced water migration toward the low-pressure surface.
   This study was undertaken with advanced magnetic resonance imaging (MRI) and magnetic resonance (MR) methods employing a MR/MRI-compatible metallic core holder. A hydrate-bearing sand pack, with 96% initial hydrate saturation, underwent dissociation by depressurization at 290 psi and 4 degrees C.