笼状水合物
水合物
多孔介质
吸附
多孔性
介孔材料
气体分离
冷凝
化学工程
化学
水煤气
碳纤维
材料科学
合成气
热力学
氢
物理化学
有机化学
催化作用
膜
复合材料
工程类
物理
生物化学
复合数
作者
Jia Liu,Yajuan Wei,Wei Meng,Pei‐Zhou Li,Yanli Zhao,Ruqiang Zou
出处
期刊:Research
[AAAS00]
日期:2019-01-01
卷期号:2019
被引量:24
标识
DOI:10.34133/2019/3206024
摘要
The reason that the stoichiometry of gas to water in artificial gas hydrates formed on porous materials is much higher than that in nature is still ambiguous. Fortunately, based on our experimental thermodynamic and kinetic study on the gas hydrate formation behavior with classic ordered mesoporous carbon CMK-3 and irregular porous activated carbon combined with density functional theory calculations, we discover a microscopic pathway of the gas hydrate formation on porous materials. Two interesting processes including (I) the replacement of water adsorbed on the carbon surface by gas and (II) further replacement of water in the pore by gas accompanied with the gas condensation in the pore and growth of gas hydrate crystals out of the pore were deduced. As a result, a great enhancement of the selectivity and regeneration for gas separation was achieved by controlling the gas hydrate formation behavior accurately.
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