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首页> 外文期刊>The Journal of Chemical Thermodynamics >Gas hydrates phase equilibria for structure I and II hydrates with chloride salts at high salt concentrations and up to 200 MPa
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Gas hydrates phase equilibria for structure I and II hydrates with chloride salts at high salt concentrations and up to 200 MPa

机译:天然气水合物适用于结构I和II的相平衡,用高盐浓度与氯化物盐加水合物,高达200MPa

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Gas hydrates phase equilibria for structure I and II hydrates with chloride salts (NaCl, CaCl2, KCl and MgCl2) were measured at high salt concentrations and up to 200 MPa. The measured equilibrium data represent three-phase (Solution - Hydrate - Vapor) or four-phase (Solution - Hydrate - Salt precipitated - Vapor) equilibrium depending on the salt concentration. The hydrate phase boundary with salts was shifted to lower temperatures and higher pressures when the experimental system was below the salt saturation concentration, while the boundaries were unchanged at salt concentrations above saturation, corresponding to quadruple points. The experimental data were compared with hydrate equilibrium predictions calculated by commonly used predictive tools to assess the reliability of these tools for the brines and conditions considered. The comparison demonstrates that predictive tools exhibit large deviation to the measured data, especially at high pressures and high salinity conditions. (C) 2017 Elsevier Ltd.
机译:在高盐浓度下测量含有氯化物盐(NaCl,CaCl 2,KCl和MgCl 2)的结构I和II水合物的气体水合物相平衡,高达200MPa。测量的平衡数据代表三相(溶液 - 水合物 - 蒸气)或四相(溶液 - 水合物 - 盐沉淀 - 蒸气),取决于盐浓度。当实验系统低于盐饱和浓度时,含有盐的水合物相边界与较低的温度和更高的压力,而在饱和的盐浓度下,边界不变,对应于四重点。将实验数据与由常用的预测工具计算的水合物平衡预测进行了比较,以评估这些工具的可靠性以及所考虑的盐水和条件。比较表明预测工具表现出对测量数据的大偏差,特别是在高压和高盐度条件下。 (c)2017年elestvier有限公司

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