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首页> 外文期刊>Fluid Phase Equilibria >Phase equilibrium for methane, ethane and carbon dioxide hydrates at pressures up to 100 MPa through high-pressure microcalorimetry: Experimental data, analysis and modeling
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Phase equilibrium for methane, ethane and carbon dioxide hydrates at pressures up to 100 MPa through high-pressure microcalorimetry: Experimental data, analysis and modeling

机译:通过高压微量微量测定法在高达100MPa的压力下甲烷,乙烷和二氧化碳水合物的相平衡:实验数据,分析和建模

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摘要

New experimental dissociation data for CH4, C2H6, and CO2 hydrates obtained by high-pressure microcalorimetry (HP-mu DSC) up to 100 MPa are presented. Deviations of onset, peak, and endset temperatures from predictions and their representativeness as equilibrium values are evaluated. For these systems, the onset temperatures provided good reproducibility and more accurate results than peak and endset temperatures, when compared to literature data. Predictions from CSMGem and Multiflash software packages are compared to the experimental results. Dynamic effects on gas hydrates formation are also evaluated by varying the water-sample size and the cooling-heating rate. Enthalpies of dissociation are determined by applying the Clapeyron equation, and new approaches are applied for the calculation of the hydrate volume and the hydration number estimation. The enthalpy of dissociation at conditions above the upper quadruple point is obtained for ethane and carbon dioxide hydrates for the first time. (C) 2020 Elsevier B.V. All rights reserved.
机译:提出了通过高压微量离核(HP-MU DSC)高达100MPa的CH 4,C2H6和CO 2水合物的新实验解离数据。评估了从预测的发病,峰值和止封温度的偏差及其代表性随着平衡值的评估。对于这些系统,与文献数据相比,起始温度提供良好的再现性和比峰值和终止的温度更准确的结果。将CSMGEM和Multiflash软件包的预测与实验结果进行了比较。还通过改变水样尺寸和冷却加热速率来评估对气体水合物形成的动态效果。通过施加苜蓿方程来确定解离的焓,并施加新方法用于计算水合物体积和水合数估计。首次获得乙烷和二氧化碳水合物以上的条件下解离的焓。 (c)2020 Elsevier B.V.保留所有权利。

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