A Review of the Effect of Porous Media on Gas Hydrate Formation

被引:47
作者
Dou, Mengyue [1 ]
Wang, Lanyun [1 ,3 ]
Wang, Yan [1 ,2 ,3 ]
Xu, Yongliang [1 ,2 ,3 ]
Li, Yao [1 ,2 ,3 ]
Chen, Yu [3 ]
Li, Lingshuang [3 ]
机构
[1] Henan Polytech Univ, Sch Safety Sci & Engn, Jiaozuo 454003, Peoples R China
[2] Collaborat Innovat Ctr coal Safety Prod & high eff, Jiaozuo 454003, Peoples R China
[3] Henan Polytech Univ, State Key Lab Cultivat Base Gas Geol & Gas Control, Jiaozuo 454003, Peoples R China
基金
中国国家自然科学基金;
关键词
METHANE HYDRATE; CARBON-DIOXIDE; PHASE-EQUILIBRIA; PORE-SIZE; ACTIVATED CARBON; CO2; CAPTURE; CH4; HYDRATE; SILICA-GELS; DISSOCIATION; KINETICS;
D O I
10.1021/acsomega.2c03048
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Most gas hydrates on the earth are in sediments and permafrost areas, and porous media are often used industrially as additives to improve gas hydrate formation. For further understanding its exploration and exploitation under natural conditions and its application in industry, it is necessary to study the effect of porous media on hydrate formation. The results show that the stacked porous media affects the phase equilibrium of hydrate formation depending on the competition water activity and large specific surface areas, while integrated porous media, such as metal foam, can transfer the hydration heat rapidly and moderate the hydrate phase equilibrium. A supersaturated metal-organic framework is able to significantly improve gas storage performance and can be used as a new material to promote hydrate formation. However, the critical particle size should be studied further for approaching the best promotion effect. In addition, together with the kinetic accelerators, porous media has a synergistic effect on gas hydrate formation. The carboxyl and hydroxyl groups on the surface of porous media can stabilize hydrate crystals through hydrogen bonding. However, the hydroxyl radicals on the silica surface inhibit the combination of CH(4 )and free water, making the phase equilibrium conditions more demanding.
引用
收藏
页码:33666 / 33679
页数:14
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