平衡和非平衡条件下烷烃溶剂/CO2/水/重油体系相行为和物理性质的定量研究

Daoyong Yang, Yunlong Li, Desheng Huang
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引用次数: 2

摘要

蒸汽-溶剂混合注入是一种很有前途的提高稠油/沥青采收率的技术,其主要机理包括溶剂(如C3H8、C4H10、CO2、N2和二甲醚)在稠油/沥青中的传热和溶解,以降低稠油/沥青的粘度和膨胀,这与溶剂/水/稠油体系的相行为密切相关。为了实现与现有油藏模拟器的无缝集成,对传统的三次状态方程(即SRK EOS和PR EOS)进行了修改和改进,以准确量化上述系统在平衡和非平衡条件下的相行为和物理性质。首先,建立了一个庞大的数据库,通过最小化水、非碳氢化合物和公共领域可获得的碳氢化合物的测量蒸汽压力与计算蒸汽压力之间的偏差来开发相应的alpha函数。用纯物质的汽化焓进一步验证了得到的α函数,并对还原温度进行了优化,重新定义了偏心因子。最后,提出了一种压力隐式策略,将稠油作为一个或多个伪组分来优化二元相互作用参数(BIPs)。此外,每种溶剂对上述系统的贡献已经在一致和统一的框架内进行了比较和分析。除了新的α函数外,还发现两个状态方程(eos)的还原温度的最佳值为0.59,而实际应用的推荐值为0.60。这种改进的EOSs已被进一步用于再现上述混合物在平衡和非平衡条件下实验测量的多相边界(或伪泡点压力)、密度、粘度、(相互)溶解度和优先传质。在CO2流中加入C3H8和/或C4H10或它们的混合物,可以增强稠油的膨胀效应。由于水的存在,等焓闪蒸可以更准确地定量溶剂-热混合过程的多相边界和物理性质。研究发现,在没有或存在多孔介质的情况下,二元或三元气体混合物的每种组分在高压和高温下优先扩散到稠油中,而在非平衡条件下,每种组分与含气饱和的稠油的溶解方式不同。
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Quantification of Phase Behaviour and Physical Properties of Alkane Solvents/CO2/ Water/Heavy Oil Systems under Equilibrium and Nonequilibrium Conditions
The hybrid steam-solvent injection has been considered as a promising technique for enhancing heavy oil/bitumen recovery, while its main mechanisms including the heat transferred and dissolution of solvents (e.g., C3H8, C4H10, CO2, N2, and DME) into heavy oil/bitumen to reduce its viscosity and swell it are closely related to the phase behaviour of the solvents/water/heavy oil systems. To allow the seamless integration with the existing reservoir simulators, the traditional cubic equations of state (i.e., SRK EOS and PR EOS) have been modified and improved to accurately quantify the phase behaviour and physical properties of the aforementioned systems under equilibrium and nonequilibrium conditions. Firstly, a huge database has been built to develop the corresponding alpha functions by minimizing the deviation between the measured and calculated vapour pressures for water as well as nonhydrocarbon and hydrocarbon compounds available from the public domain. Such obtained alpha functions are further validated with enthalpy of vaporization for pure substances, and then the reduced temperature has been optimized and the eccentric factor has been redefined. Finally, a pressure-implicit strategy has been developed to optimize the binary interaction parameters (BIPs) by treating heavy oil as one pseudocomponent (PC) or multiple PCs. Also, the contributions of each solvent to the aforementioned systems have been compared and analyzed within a consistent and unified framework. In addition to new alpha functions for hydrocarbons and water, respectively, the reduced temperature is found to have its optimum value of 0.59 for the two equations of state (EOSs), while 0.60 is recommended for practical use. Such improved EOSs have been further employed to reproduce the experimentally measured multiphase boundaries (or pseudo-bubble-point pressures), density, viscosity, (mutual) solubility, and preferential mass transfer for the aforementioned mixtures under equilibrium and nonequilibrium conditions. The swelling effect for the heavy oil can be enhanced due to the addition of C3H8 and/or C4H10 or their mixtures into the CO2 stream. Due to the existence of water, isenthalpic flash leads to more accurate quantification of multiphase boundaries and physical properties for the hybrid solvent-thermal processes. Each component of a binary or ternary gas mixture is found to diffuse preferentially into heavy oil at high pressures and elevated temperatures in the absence and presence of porous media, while each of them is found to exsolve differently from gas-saturated heavy oil under nonequilibrium conditions.
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