Insight into increased stability of methane hydrates at high pressure from phase equilibrium data and molecular structure
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Insight into increased stability of methane hydrates at high pressure from phase equilibrium data and molecular structure

机译:从相平衡数据和分子结构高压下高压下甲烷水合物的稳定性增加

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Abstract The methane hydrate dissociation conditions are measured at high pressures (up to 200?MPa) to fundamentally understand the hydrate properties. The results show an increased enthalpy of dissociation, from about 53 to 58?kJ/mol, as the hydrate equilibrium pressures transition from low (80?MPa) to higher pressures (up to 200?MPa), indicating greater stability for the hydrates. Molecular simulations are used to understand and explain the increased stability with increasing pressure, by calculating the enthalpy and molecular structure of the phases. Graphical abstract Display Omitted ]]>
机译:<![CDATA [ 抽象 甲烷水合物解离条件以高压(最多200μmba)测量,从而从根本上了解水合物性质。结果表明,随着水合物平衡压力从低(<80℃)转变为更高的压力(最多200≤MPa),从约53至58Ω·kJ / mol的焓增加了焓增加,表明更大的稳定性水合物。通过计算阶段的焓和分子结构,使用分子模拟来了解和解释随着压力的增加而增加的稳定性。 图形抽象 显示省略 ]]>

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