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Phase behavior of C3H8-CO2-heavy oil systems in the presence of aqueous phase under reservoir conditions

机译:储层条件下在水相存在下C3H8-CO2-重油体系的相行为

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摘要

Phase behaviors including phase boundaries, volumes, and compositions of reservoir fluids during solvent(s)-assisted heavy oil recovery processes have been experimentally and theoretically determined in the presence of an aqueous phase. More specifically, a water-rich aqueous phase (A), an oil-rich liquid phase (L), and a solvents-rich vapor phase (V) can coexist under certain reservoir conditions. The phase boundary between AL and ALV on a pressure-temperature phase diagram, i.e., three-phase bubblepoint pressure, has been measured for C3H8-CO2-water-heavy oil systems at temperature ranging from 298.15 K to 383.15 K. The phase volumes of A + L and V at thermodynamic equilibrium state have been determined at temperatures of 321.55 K and 344.95 K, respectively. Moreover, the fluids in both L and V phases are sampled in an isobaric manner to perform the compositional analyses by using gas chromatography (GC) method. Meanwhile, two heavy oil samples are theoretically characterized as the multiple pseudocomponents. The Peng-Robinson equation of state (PR EOS) together with two recently developed alpha functions for water and non-water component(s) is applied as the primary thermodynamic model. A previously developed binary interaction parameter (BIP) correlation for CO2-water pair is combined with the van der Waals' mixing rule to improve the phase behavior prediction for water-contained system. A volume translation method proposed by Peneloux et al. (1982) is then incorporated to correct the calculated phase volume. Without tuning any parameters, the developed water-associated and water-free mathematical models are found to be able to accurately reproduce the measured phase boundaries in the presence and absence of the aqueous phase, respectively. The three-phase bubblepoint pressure is found to be reduced in the presence of water. More accurate prediction can be achieved by considering the effect of aqueous phase. Finally, the GC analyses and flash calculations demonstrate that CO2 is more easily to be vaporized than alkane solvent (i.e., C3H8) when phase splitting occurs for a C3H8-CO2-water-heavy oil system.
机译:已经在水相存在下通过实验和理论确定了溶剂辅助重油采收过程中的相行为,包括相边界,体积和储层流体的组成。更具体地,在某些储层条件下,富水水相(A),富油液相(L)和富溶剂气相(V)可以共存。在压力-温度相位图上,即在三相蒸汽点压力下,对于C3H8-CO2-水-重油系统,已测量了AL和ALV之间的相界,温度范围为298.15 K至383.15K。在热力学平衡状态下的A + L和V分别在321.55 K和344.95 K的温度下确定。此外,以等压方式对L相和V相中的流体进行采样,以通过使用气相色谱(GC)方法进行组成分析。同时,理论上将两个重油样品表征为多个假组分。 Peng-Robinson状态方程(PR EOS)以及两个最近开发的针对水和非水成分的alpha函数被用作主要的热力学模型。将先前开发的用于CO2-水对的二元相互作用参数(BIP)相关性与范德华斯混合规则结合起来,以改进含水系统的相行为预测。 Peneloux等人提出的体积翻译方法。 (1982)然后被合并以校正计算的相体积。在不调整任何参数的情况下,发现开发的水相关和无水数学模型能够分别在存在和不存在水相的情况下准确地重现所测量的相界。发现在水的存在下三相泡点压力降低。通过考虑水相的影响可以实现更准确的预测。最后,GC分析和闪蒸计算表明,当C3H8-CO2-水-重油系统发生分相时,CO2比烷烃溶剂(即C3H8)更容易蒸发。

著录项

  • 来源
    《Fuel》 |2017年第1期|358-370|共13页
  • 作者单位

    Univ Kansas, Chem & Petr Engn, Sch Engn, Lawrence, KS 66045 USA|Univ Regina, Fac Engn & Appl Sci, Petr Syst Engn, Regina, SK S4S 0A2, Canada;

    PetroChina, Res Inst Petr Explorat & Dev, Beijing, Peoples R China;

    Univ Regina, Fac Engn & Appl Sci, Petr Syst Engn, Regina, SK S4S 0A2, Canada;

    PetroChina, Res Inst Petr Explorat & Dev, Beijing, Peoples R China;

    PetroChina, Res Inst Petr Explorat & Dev, Beijing, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Phase behavior; C3H8-CO2-water-heavy oil systems; Solvents-assisted EOR; PVT experiment; Equation of state;

    机译:相行为;C3H8-CO2-水重油系统;溶剂辅助的EOR;PVT实验;状态方程;

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