Modification of a thermodynamic model and an equation of state for accurate calculation of asphaltene precipitation phase behavior

Fuel ◽  
2008 ◽  
Vol 87 (1) ◽  
pp. 85-91 ◽  
Author(s):  
M. Nikookar ◽  
G.R. Pazuki ◽  
M.R. Omidkhah ◽  
L. Sahranavard
1992 ◽  
Vol 57 (7) ◽  
pp. 1362-1372 ◽  
Author(s):  
Roumiana P. Stateva ◽  
Stefan G. Tsvetkov

The paper discusses modelling of the multiphase behavior of the methane-ethane-nitrogen mixture, which is of a considerable interest for the natural gas and oil industries. The thermodynamic model is a modified Redlich-Kwong-Soave equation of state. The computer algorithm is based on a new approach to solving the isothermal multiphase flash problem, when the number and identity of the phases present at equilibrium are unknown in advance. The results demonstrate that Redlich-Kwong-Soave equation of state and the algorithm applied predict with reasonable accuracy the complicated phase behavior and the region of L1L2V equilibrium, observed in the experiment, of the methane-ethane-nitrogen system.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ilyas Al-Kindi ◽  
Tayfun Babadagli

AbstractThe thermodynamics of fluids in confined (capillary) media is different from the bulk conditions due to the effects of the surface tension, wettability, and pore radius as described by the classical Kelvin equation. This study provides experimental data showing the deviation of propane vapour pressures in capillary media from the bulk conditions. Comparisons were also made with the vapour pressures calculated by the Peng–Robinson equation-of-state (PR-EOS). While the propane vapour pressures measured using synthetic capillary medium models (Hele–Shaw cells and microfluidic chips) were comparable with those measured at bulk conditions, the measured vapour pressures in the rock samples (sandstone, limestone, tight sandstone, and shale) were 15% (on average) less than those modelled by PR-EOS.


Energies ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1315
Author(s):  
Jingwei Huang ◽  
Hongsheng Wang

Confined phase behavior plays a critical role in predicting production from shale reservoirs. In this work, a pseudo-potential lattice Boltzmann method is applied to directly model the phase equilibrium of fluids in nanopores. First, vapor-liquid equilibrium is simulated by capturing the sudden jump on simulated adsorption isotherms in a capillary tube. In addition, effect of pore size distribution on phase equilibrium is evaluated by using a bundle of capillary tubes of various sizes. Simulated coexistence curves indicate that an effective pore size can be used to account for the effects of pore size distribution on confined phase behavior. With simulated coexistence curves from pore-scale simulation, a modified equation of state is built and applied to model the thermodynamic phase diagram of shale oil. Shifted critical properties and suppressed bubble points are observed when effects of confinement is considered. The compositional simulation shows that both predicted oil and gas production will be higher if the modified equation of state is implemented. Results are compared with those using methods of capillary pressure and critical shift.


Author(s):  
Syed Imran Ali ◽  
Javed Haneef ◽  
Syed Talha Tirmizi ◽  
Shaine Mohammadali Lalji ◽  
Anas Nabil Sallam Hezam

2016 ◽  
Author(s):  
Ali Abouie ◽  
Mohsen Rezaveisi ◽  
Saeedeh Mohebbinia ◽  
Kamy Sepehrnoori

SPE Journal ◽  
2018 ◽  
Vol 24 (02) ◽  
pp. 647-659 ◽  
Author(s):  
V. A. Torrealba ◽  
R. T. Johns ◽  
H.. Hoteit

Summary An accurate description of the microemulsion-phase behavior is critical for many industrial applications, including surfactant flooding in enhanced oil recovery (EOR). Recent phase-behavior models have assumed constant-shaped micelles, typically spherical, using net-average curvature (NAC), which is not consistent with scattering and microscopy experiments that suggest changes in shapes of the continuous and discontinuous domains. On the basis of the strong evidence of varying micellar shape, principal micellar curves were used recently to model interfacial tensions (IFTs). Huh's scaling equation (Huh 1979) also was coupled to this IFT model to generate phase-behavior estimates, but without accounting for the micellar shape. In this paper, we present a novel microemulsion-phase-behavior equation of state (EoS) that accounts for changing micellar curvatures under the assumption of a general-prolate spheroidal geometry, instead of through Huh's equation. This new EoS improves phase-behavior-modeling capabilities and eliminates the use of NAC in favor of a more-physical definition of characteristic length. Our new EoS can be used to fit and predict microemulsion-phase behavior irrespective of IFT-data availability. For the cases considered, the new EoS agrees well with experimental data for scans in both salinity and composition. The model also predicts phase-behavior data for a wide range of temperature and pressure, and it is validated against dynamic scattering experiments to show the physical significance of the approach.


SPE Journal ◽  
2011 ◽  
Vol 16 (04) ◽  
pp. 921-930 ◽  
Author(s):  
Antonin Chapoy ◽  
Rod Burgass ◽  
Bahman Tohidi ◽  
J. Michael Austell ◽  
Charles Eickhoff

Summary Carbon dioxide (CO2) produced by carbon-capture processes is generally not pure and can contain impurities such as N2, H2, CO, H2 S, and water. The presence of these impurities could lead to challenging flow-assurance issues. The presence of water may result in ice or gas-hydrate formation and cause blockage. Reducing the water content is commonly required to reduce the potential for corrosion, but, for an offshore pipeline system, it is also used as a means of preventing gas-hydrate problems; however, there is little information on the dehydration requirements. Furthermore, the gaseous CO2-rich stream is generally compressed to be transported as liquid or dense-phase in order to avoid two-phase flow and increase in the density of the system. The presence of impurities will also change the system's bubblepoint pressure, hence affecting the compression requirement. The aim of this study is to evaluate the risk of hydrate formation in a CO2-rich stream and to study the phase behavior of CO2 in the presence of common impurities. An experimental methodology was developed for measuring water content in a CO2-rich phase in equilibrium with hydrates. The water content in equilibrium with hydrates at simulated pipeline conditions (e.g., 4°C and up to 190 bar) as well as after simulated choke conditions (e.g., at -2°C and approximately 50 bar) was measured for pure CO2 and a mixture of 2 mol% H2 and 98 mol% CO2. Bubblepoint measurements were also taken for this binary mixture for temperatures ranging from -20 to 25°C. A thermodynamic approach was employed to model the phase equilibria. The experimental data available in the literature on gas solubility in water in binary systems were used in tuning the binary interaction parameters (BIPs). The thermodynamic model was used to predict the phase behavior and the hydrate-dissociation conditions of various CO2-rich streams in the presence of free water and various levels of dehydration (250 and 500 ppm). The results are in good agreement with the available experimental data. The developed experimental methodology and thermodynamic model could provide the necessary data in determining the required dehydration level for CO2-rich systems, as well as minimum pipeline pressure required to avoid two-phase flow, hydrates, and water condensation.


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