成核
水合物
甲烷
笼状水合物
化学工程
高定向热解石墨
化学
石墨
热解炭
化学物理
材料科学
有机化学
热解
工程类
作者
Yong Guo,Wei Xiao,Wanfen Pu,Jun Hu,Jinzhou Zhao,Lijuan Zhang
出处
期刊:Langmuir
[American Chemical Society]
日期:2018-08-02
卷期号:34 (34): 10181-10186
被引量:57
标识
DOI:10.1021/acs.langmuir.8b01900
摘要
The surface hydrophobicity of solid particles plays a critical role in the nucleation of gas hydrate formation, and it was found that the hydrophobic surface will promote this nucleation process, but the underlying mechanism is still unveiled. Herein, we proposed for the first time our new theory that the formation of methane nanoscale gas bubbles on the hydrophobic surface provides the nuclei sites for further formation of methane hydrate. First, we studied the effect of hydrophobicity of particles on the nucleation of hydrate. It was found that the hydrophobic graphite and silica particles would promote the nucleation of hydrate, but the hydrophilic silica particles did not promote the methane hydrate nucleation. Then, we designed the atomic force microscopy experiment to explain this mechanism from a nanometer scale. The results showed that the methane nanobubbles were formed on the hydrophobic highly ordered pyrolytic graphite surface, but they were hard to form on the hydrophilic mica surface. These results indicated that the methane nanobubbles on the hydrophobic surface could provide the gas hydrate nucleation sites and may induce a rapid nucleation of methane hydrate.
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