Phase Behavior Modeling of Alkyl Amine + Hydrocarbon and Alkyl Amine + Alcohol Systems Using a Group Contribution Associating Equation of State

2009 ◽  
Vol 48 (16) ◽  
pp. 7705-7712 ◽  
Author(s):  
Francisco A. Sánchez ◽  
Amir H. Mohammadi ◽  
Alfonsina Andreatta ◽  
Selva Pereda ◽  
Esteban Brignole ◽  
...  
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.


2020 ◽  
Vol 65 (12) ◽  
pp. 5862-5890
Author(s):  
Andrew J. Haslam ◽  
Alfonso González-Pérez ◽  
Silvia Di Lecce ◽  
Siti H. Khalit ◽  
Felipe A. Perdomo ◽  
...  

2014 ◽  
Vol 59 (10) ◽  
pp. 3272-3288 ◽  
Author(s):  
Simon Dufal ◽  
Vasileios Papaioannou ◽  
Majid Sadeqzadeh ◽  
Thomas Pogiatzis ◽  
Alexandros Chremos ◽  
...  

AIChE Journal ◽  
2009 ◽  
Vol 55 (5) ◽  
pp. 1265-1273 ◽  
Author(s):  
Eliane Kühne ◽  
Angel Martin ◽  
Geert-Jan Witkamp ◽  
Cor J. Peters

SPE Journal ◽  
2018 ◽  
Vol 23 (05) ◽  
pp. 1899-1908 ◽  
Author(s):  
V. A. Torrealba ◽  
R. T. Johns

Summary Surfactant-mediated enhanced-oil-recovery (EOR) techniques, such as surfactant/polymer (SP) flooding, have received increased attention because of their ability to reduce capillary forces at the pore-scale to ultralow values and mobilize trapped oil. Recently, there have been increased efforts in microemulsion-phase-behavior modeling capabilities by relying on the hydrophilic/lipophilic-difference (HLD) measure for surfactant-affinity quantification. One common assumption of most microemulsion-phase-behavior models is the assumption of pure excess phases, which states that the surfactant component is only present in the microemulsion phase. This assumption can lead to significant errors for some surfactant systems, especially when applied to chemical simulations in which discontinuities may arise. The main novelty of this paper is to allow for surfactant partitioning into both the water and oil excess phases by use of a simple approach, and then relate relevant surfactant-partitioning coefficients (i.e., K-values) to HLD. Surfactant screening that is based on surfactant-structure parameters is also considered based on estimated K-values. Key dimensionless groups are identified as a function of activity coefficients, which allow for a simplified description of the surfactant-partition coefficients. These surfactant-partition coefficients are combined with the chemical-potentials (CP) equation-of-state (EoS) model to describe and predict the phase behavior when the excess phases are not pure. Further, the developed surfactant-partitioning model can be used in other microemulsion-phase-behavior models to allow for impure excess phases.


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