Bubble Point Pressures of Hydrocarbon Mixtures in Multiscale Volumes from Density Functional Theory

被引:24
|
作者
Zhao, Yinuo [1 ]
Wang, Yingnan [1 ]
Zhong, Junjie [2 ]
Xu, Yi [2 ]
Sinton, David [2 ]
Jin, Zhehui [1 ]
机构
[1] Univ Alberta, Sch Min & Petr Engn, Dept Civil & Environm Engn, Edmonton, AB T6G 1H9, Canada
[2] Univ Toronto, Dept Mech & Ind Engn, 5 Kings Coll Rd, Toronto, ON M5S 3G8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
PORE-SIZE DISTRIBUTION; PHASE-BEHAVIOR; SHALE GAS; ADSORPTION; CONFINEMENT; CONDENSATION; HYSTERESIS; SOLVATION; NANOPORES;
D O I
10.1021/acs.langmuir.8b02789
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Accurate characterization of the bubble point pressure of hydrocarbon mixtures under nanoconfinement is crucial to the prediction of ultimate oil recovery and well productivity of shale/tight oil reservoirs. Unlike conventional reservoirs, shale has an extensive network of tiny pores in the range of a few nanometers. In nanopores, the properties of hydrocarbon fluids deviate from those in bulk because of significant surface adsorption. Many previous theoretical works use a conventional equation of state model coupled with capillary pressure to study the nanoconfinement effect. Without including the inhomogeneous molecular density distributions in nanoconfinement, these previous approaches predict only slightly reduced bubble points. In this work, we use density functional theory to study the effect of nanoconfinement on the hydrocarbon mixture bubble point pressure by explicitly considering fluid-surface interactions and inhomogeneous density distributions in nanopores. We find that as system pressure decreases, while lighter components are continuously released from the nanopores, heavier components accumulate within. The bubble point pressure of nanoconfined hydrocarbon mixtures is thus significantly suppressed from the bulk bubble point to below the bulk dew point, in line with our previous experiments. When bulk fluids are in a two-phase, the confined hydrocarbon fluids are in a single liquid-like phase. As pore size increases, bubble point pressure of confined fluids increases and hydrocarbon average density in nanopores approaches the liquid-phase density in bulk when bulk is in a two-phase region. For a finite volume bulk bath, we find that because of the competitive adsorption in nanopores, the bulk bubble point pressure increases in line with a previous experimental work. Our work demonstrates how mixture dynamics and nanopore-bulk partitioning influence phase behavior in nanoconfinement and enables the accurate estimation of hydrocarbon mixture bubble point pressure in shale nanopores.
引用
收藏
页码:14058 / 14068
页数:11
相关论文
共 50 条
  • [41] Multiscale time-dependent density functional theory: Demonstration for plasmons
    Jiang, Jiajian
    Mansour, Andrew Abi
    Ortoleva, Peter J.
    JOURNAL OF CHEMICAL PHYSICS, 2017, 147 (05):
  • [42] Bubble gating in biological ion channels: A density functional theory study
    Gussmann, Florian
    Roth, Roland
    PHYSICAL REVIEW E, 2017, 95 (06)
  • [43] Theory of melting at high pressures: Amending density functional theory with quantum Monte Carlo
    Shulenburger, L.
    Desjarlais, M. P.
    Mattsson, T. R.
    PHYSICAL REVIEW B, 2014, 90 (14)
  • [44] Heats of adsorption and pore pressures predicted by classical density functional theory
    Hlushak, Stepan
    LeVan, Douglas
    Cummings, Peter
    McCabe, Clare
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2014, 247
  • [45] Density functional theory approach to colloid-polymer mixtures
    Roth, Roland
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2010, 239
  • [46] Density functional theory for colloidal rod-sphere mixtures
    Schmidt, M
    PHYSICAL REVIEW E, 2001, 63 (05): : 502011 - 502014
  • [47] An investigation of dynamical density functional theory for solvation in simple mixtures
    Yoshimori, A
    Day, TJF
    Patey, GN
    JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (15): : 6378 - 6386
  • [48] Density functional theory of inhomogeneous mixtures of polymeric fluids.
    Wu, JZ
    Yu, YX
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2003, 225 : U630 - U630
  • [49] Investigation of dynamical density functional theory for solvation in simple mixtures
    Yoshimori, Akira
    Day, Tyler J.F.
    Patey, G.N.
    Journal of Chemical Physics, 1998, 108 (15):
  • [50] Density functional theory: Structure and interfacial properties of binary mixtures
    Wadewitz, T
    Winkelmann, J
    BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1996, 100 (11): : 1825 - 1832