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Influence of gravitational potential on the thermodynamic stability of pure and mixed clathrate hydrates

机译:引力潜力对纯和混合克拉碱水合物热力学稳定性的影响

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摘要

Clathrate hydrates are an ice-like material consisting of gas molecules confined within cavities in a crystalline water lattice. Phase equilibria of clathrate hydrates systems was described using the statistical mechanical theory of van der Waals and Platteeuw. This theory makes use of the fractional occupancy of cavities within the clathrate hydrate lattice in the determination of chemical equilibria. Classical density functional theory with intermolecular interactions restricted to the first hydration shell was employed to determine the fractional occupancy. In addition to the external field describing the gas-water interactions, the effect of a gravitational field was introduced. The results of the calculations show that although the gravitational potential term may be orders of magnitude smaller than the thermal kinetic energy of the gas species or the hydrogen-bond energy holding the clathrate lattice together, it can nevertheless influence the phase equilibrium of the clathrate hydrate system to some degree. The effect of the magnitudes of both the gravitational potential and the local gravitational field are considered too.
机译:Clathrate水合物是一种冰状材料,其由狭窄在结晶水晶格中的空腔内的气体分子组成。使用van der waals和platteeuw的统计机械理论描述了Clathrate水合物系统的相平衡。该理论利用Clathrate水合物晶格内的腔体的分数占据在测定化学均衡中。使用限制第一水合壳的分子间相互作用的经典密度函数理论来确定分数占用。除了描述气水相互作用的外部领域之外,引入了引力场的效果。计算结果表明,尽管引力势术语可以是小于气体物种的热动能的数量级或将包合物晶格保持在一起的氢键能量,但它仍然可以影响包裹水合物的相平衡系统到某种程度。考虑了重力电位和局部重力场的幅度的影响。

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