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水合物在气-液界面上生长的非平衡热力学。

Nonequilibrium Thermodynamics of Hydrate Growth on a Gas-Liquid Interface.

机构信息

Massachusetts Institute of Technology, 77 Massachusetts Avenue, Building 1, Cambridge, Massachusetts 02139, USA.

Technical University of Madrid, Calle del Profesor Aranguren 3, 28040 Madrid, Spain.

出版信息

Phys Rev Lett. 2018 Apr 6;120(14):144501. doi: 10.1103/PhysRevLett.120.144501.

Abstract

We develop a continuum-scale phase-field model to study gas-liquid-hydrate systems far from thermodynamic equilibrium. We design a Gibbs free energy functional for methane-water mixtures that recovers the isobaric temperature-composition phase diagram under thermodynamic equilibrium conditions. The proposed free energy is incorporated into a phase-field model to study the dynamics of hydrate formation on a gas-liquid interface. We elucidate the role of initial aqueous concentration in determining the direction of hydrate growth at the interface, in agreement with experimental observations. Our model also reveals two stages of hydrate growth at an interface-controlled by a crossover in how methane is supplied from the gas and liquid phases-which could explain the persistence of gas conduits in hydrate-bearing sediments and other nonequilibrium phenomena commonly observed in natural methane hydrate systems.

摘要

我们开发了一个连续统相场模型来研究远离热力学平衡的气-液-水合物系统。我们为甲烷-水混合物设计了一个 Gibbs 自由能泛函,该泛函在热力学平衡条件下恢复等压温度-组成相图。所提出的自由能被纳入一个相场模型中,以研究气-液界面上水合物形成的动力学。我们阐明了初始水浓度在确定界面上水合物生长方向方面的作用,这与实验观察结果一致。我们的模型还揭示了界面控制下的水合物生长的两个阶段,这是由甲烷从气相和液相供应方式的转变决定的-这可以解释在含有水合物的沉积物中气体通道的持久性以及在自然甲烷水合物系统中通常观察到的其他非平衡现象。

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