成核
笼状水合物
水合物
化学物理
化学
背景(考古学)
材料科学
热力学
化学工程
有机化学
物理
地质学
工程类
古生物学
作者
Zhengcai Zhang,Peter G. Kusalik,Guang-Jun Guo,Yanlong Li,Lixin Huang,Nengyou Wu
标识
DOI:10.1021/acs.jpclett.4c03074
摘要
Nucleation of multicomponent systems is a pervasive phenomenon in nature and is pertinent to a diverse array of scientific and industrial challenges. The nucleation mechanisms of immiscible multicomponent systems remain unclear. Here, gas hydrate is employed as a model system to study the nucleation of multicomponent systems. The effect of gas/liquid and solid/liquid interfaces on hydrate nucleation is examined through molecular dynamics simulations. The results demonstrate that gas hydrates tend to nucleate in the solution phase in the proximity of the gas/liquid interface at lower temperatures, which is controlled by mass transfer. As the temperature increases, the location of hydrate nucleation gradually shifts from the gas/liquid interface to the solid/liquid interface. We anticipate that the nucleation free energy barrier dominates the hydrate nucleation process at these conditions, making the heterogeneous nucleation with a lower free energy barrier more probable. The findings provide molecular insights into the mechanism and pathway underlying interface-induced gas hydrate nucleation. These insights will inform the development of the theory of gas hydrate nucleation, particularly in the context of heterogeneous nucleation.
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