scholarly journals Experimental and Computational Modeling of Microemulsion Phase Behavior

2021 ◽  
Author(s):  
Vai Yee Hon ◽  
Ismail B.M. Saaid

The phase behavior of microemulsions formed in a surfactant-brine-oil system for a chemical Enhanced Oil Recovery (EOR) application is complex and depends on a range of parameters. Phase behavior indicates a surfactant solubilization. Phase behavior tests are simple but time-consuming especially when it involves a wide range of surfactant choices at various concentrations. An efficient and insightful microemulsion formulation via computational simulation can complement phase behavior laboratory test. Computational simulation can predict various surfactant properties, including microemulsion phase behavior. Microemulsion phase behavior can be predicted predominantly using Quantitative Structure-Property Relationship (QSPR) model. QSPR models are empirical and limited to simple pure oil system. Its application domain is limited due to the model cannot be extrapolated beyond reference condition. Meanwhile, there are theoretical models based on physical chemistry of microemulsion that can predict microemulsion phase behavior. These models use microemulsion surface tension and torque concepts as well as with solution of bending rigidity of microemulsion interface with relation to surface solubilization and interface energy.

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.


1982 ◽  
Vol 22 (06) ◽  
pp. 962-970 ◽  
Author(s):  
J. Novosad

Novosad, J., SPE, Petroleum Recovery Inst. Abstract Experimental procedures designed to differentiate between surfactant retained in porous media because of adsorption and surfactant retained because Of unfavorable phase behavior are developed and tested with three types of surfactants. Several series of experiments with systematic changes in one variable such as surfactant/cosurfactant ratio, slug size, or temperature are performed, and overall surfactant retention then is interpreted in terms of adsorption and losses caused by unfavorable phase behavior. Introduction Adsorption of surfactants considered for enhanced oil recovery (EOR) applications has been studied extensively in the last few years since it has been shown that it is possible to develop surfactant systems that displace oil from porous media almost completely when used in large quantities. Effective oil recovery by surfactants is not a question of principle but rather a question of economics. Since surfactants are more expensive than crude oil, development of a practical EOR technology depends on how much surfactant can be sacrificed economically while recovering additional crude oil from a reservoir.It was recognized earlier that adsorption may be only one of a number of factors that contribute to total surfactant retention. Other mechanisms may include surfactant entrapment in an immobile oil phase surfactant precipitation by divalent ions, surfactant precipitation caused by a separation of the cosurfactant from the surfactant, and surfactant precipitation resulting from chromatographic separation of different surfactant specks. The principal objective of this work is to evaluate the experimental techniques that can be used for measuring surfactant adsorption and to study experimentally two mechanisms responsible for surfactant retention. Specifically, we try to differentiate between the adsorption of surfactants at the solid/liquid interface and the retention of the surfactants because of trapping in the immobile hydrocarbon phase that remains within the core following a surfactant flood. Measurement of Adsorption at the Solid/Liquid Interface Previous adsorption measurements of surfactants considered for EOR produced adsorption isotherms of unusual shapes and unexpected features. Primarily, an adsorption maximum was observed when total surfactant retention was plotted against the concentration of injected surfactant. Numerous explanations have been offered for these peaks, such as a formation of mixed micelles, the effects of structure-forming and structurebreaking cations, and the precipitation and consequent redissolution of divalent ions. It is difficult to assess which of these effects is responsible for the peaks in a particular situation and their relative importance. However, in view of the number of physicochemical processes taking place simultaneously and the large number of components present in most systems, it seems that we should not expect smooth monotonically increasing isotherms patterned after adsorption isothemes obtained with one pure component and a solvent. Also, it should be realized that most experimental procedures do not yield an amount of surfactant adsorbed but rather a measure of the surface excess.An adsorption isotherm, expressed in terms of the surface excess as a function of an equilibrium surfactant concentration, by definition must contain a maximum if the data are measured over a sufficiently wide range of concentrations. SPEJ P. 962^


Author(s):  
Saba Mahmoudvand ◽  
Behnam Shahsavani ◽  
Rafat Parsaei ◽  
Mohammad Reza Malayeri

The depletion of oil reservoirs and increased global oil demand have given impetus to employ various secondary and tertiary oil recovery methods. Gas injection is widely used in both secondary and tertiary modes, though the major problem associated with this process is the precipitation and deposition of asphaltene, particularly at near-wellbore conditions. In-depth knowledge of asphaltene phase behavior is therefore essential for the prediction of asphaltene precipitation. Previous studies reported the impact of gas injection on asphaltene phase behavior, but the knowledge of precipitation of asphaltene as a function of different mole fractions of injected gas is also imperative. In this study, the thermodynamic model of PC-SAFT EoS is used to discern the phase equilibrium of asphaltene by analyzing the asphaltene drop-out curve during gas injection. Asphaltene drop-out curves of two different live oil samples are analyzed by injecting CO2, CH4, and N2 gases at different mole percentages and temperatures. The results revealed that PC-SAFT EoS can serve as a reliable tool for estimating bubble pressure and asphaltene onset pressure for a wide range of temperatures, pressures, and compositions. The simulation results for the injection of CO2, CH4, and N2 also showed that CO2 gas gives minimum asphaltene precipitation. It reduces the size of the drop-out curve or moves it toward higher pressures. CH4 and N2 expand the drop-out curve by raising the upper onset point. CH4 increases the maximum point of the drop-out curve for two types of oil studied (A and B) at two different temperatures. N2 raises the maximum point of oil type “A” by approximately 57% at 395 K, while it has no effect on the maximum point of oil type “B”. In addition, reducing the temperature resulted in either decrease or increase of asphaltene solubility, demonstrating that the impact of temperature on asphaltene precipitation is closely related to the composition of the crude.


2007 ◽  
Vol 10 (05) ◽  
pp. 482-488 ◽  
Author(s):  
Kristian Jessen ◽  
Erling Halfdan Stenby

Summary Accurate performance prediction of miscible enhanced-oil-recovery (EOR) projects or CO2 sequestration in depleted oil and gas reservoirs relies in part on the ability of an equation-of-state (EOS) model to adequately represent the properties of a wide range of mixtures of the resident fluid and the injected fluid(s). The mixtures that form when gas displaces oil in a porous medium will, in many cases, differ significantly from compositions created in swelling tests and other standard pressure/volume/temperature (PVT) experiments. Multicontact experiments (e.g., slimtube displacements) are often used to condition an EOS model before application in performance evaluation of miscible displacements. However, no clear understanding exists of the impact on the resultant accuracy of the selected characterization procedure when the fluid description is subsequently included in reservoir simulation. In this paper, we present a detailed analysis of the quality of two different characterization procedures over a broad range of reservoir fluids (13 samples) for which experimental swelling-test and slimtube-displacement data are available. We explore the impact of including swelling-test and slimtube experiments in the data reduction and demonstrate that for some gas/oil systems, swelling tests do not contribute to a more accurate prediction of multicontact miscibility. Finally, we report on the impact that use of EOS models based on different characterization procedures can have on recovery predictions from dynamic 1D displacement calculations. Introduction During the past few decades, a significant effort has been invested in the studies and development of improved-oil-recovery processes. From a technical point of view, gas injection can be a very efficient method for improving the oil production, particularly in the case when miscibility develops during the displacement process. The lowest pressure at which a gas should be injected into the reservoir to obtain the multicontact miscible displacement—the minimum miscibility pressure (MMP)—has consequently attained a very important status in EOR studies. Various methods for measuring and calculating the MMP have been proposed in the literature. Many of these are based on simplifications such as the ternary representation of the compositional space. This method fails to honor the existence of a combined mechanism controlling the development of miscibility in real reservoir fluids. Zick (1986) and Stalkup (1987) described the existence of the condensing/vaporizing mechanism. They showed that the development of miscibility (MMP) in multicomponent gas-displacement processes could, independent of the mechanism controlling the development of miscibility, be predicted accurately by 1D compositional simulations. A semianalytical method for predicting the MMP was later presented by Wang and Orr (1997), who played an important role in the development and application of the analytical theory of gas-injection processes. Jessen et al. (1998) subsequently developed an efficient algorithm for performing these calculations, reducing the MMP calculation time to a few seconds even for fluid descriptions of 10 components or more. Later, Jessen et al. (2001) used this approach to generate approximate solutions to the dispersion-free, 1D-displacement problem for multicomponent gas-injection processes. Analytical and numerical methods for predicting the performance of a gas-injection process depend on an EOS to predict the phase behavior of the mixtures that form in the course of a displacement process. The role of the phase behavior in relation to numerical diffusion in compositional reservoir simulation has been pointed out previously by Stalkup (1990) and by Stalkup et al. (1990). Recently, Jessen et al. (2004) proposed a method to quantify the interplay of the phase behavior and numerical diffusion in a finite-difference simulation of a gas-injection process. By analyzing the phase behavior of the injection-gas/reservoir-fluid system, a measure of the impact, referred to as the dispersive distance, can be calculated. The dispersive distance is useful when designing and interpreting large-scale compositional reservoir simulations.


SPE Journal ◽  
2014 ◽  
Vol 20 (02) ◽  
pp. 255-266 ◽  
Author(s):  
R.. Fortenberry ◽  
D.H.. H. Kim ◽  
N.. Nizamidin ◽  
S.. Adkins ◽  
G.W.. W. Pinnawala Arachchilage ◽  
...  

Summary We have found that the addition of low concentrations of certain inexpensive light cosolvents to alkaline/polymer (AP) solutions dramatically improves the performance of AP corefloods in two important ways. First, the addition of cosolvent promotes the formation of low-viscosity microemulsions rather than viscous macroemulsions. Second, these light cosolvents greatly improve the phase behavior in a way that can be tailored to a particular oil, temperature, and salinity. This new chemical enhanced-oil-recovery (EOR) technology uses polymer for mobility control and has been termed alkali/cosolvent/polymer (ACP) flooding. ACP corefloods perform as well as alkaline/surfactant/polymer (ASP) corefloods while being simpler and more robust. We report 12 successful ACP corefloods using four different crude oils ranging from 12 to 24°API. The ACP process shows special promise for heavy oils, which tend to have large fractions of soap-forming acidic components, but is applicable across a wide range of oil gravity.


SPE Journal ◽  
2013 ◽  
Vol 18 (06) ◽  
pp. 1140-1149 ◽  
Author(s):  
Alireza Iranshahr ◽  
Denis V. Voskov ◽  
Hamdi A. Tchelepi

Summary Enhanced Oil Recovery (EOR) processes usually involve complex phase behavior between the injected fluid (e.g., steam, hydrocarbon, CO2, sour gas) and the in-situ rock-fluid system. Several fundamental questions remain regarding Equation-of-State (EOS) computations for mixtures that can form three, or more, phases at equilibrium. In addition, numerical and computational issues related to the proper coupling of the thermodynamic phase behavior with multi-component transport must be resolved to accurately and efficiently model the behavior of large-scale EOR processes. Previous work has shown that the adaptive tabulation of tie-simplexes in the course of a compositional simulation is a reliable alternative to the conventional EOS-based compositional simulation. In this paper, we present the numerical results of reservoir flow simulation with adaptive tie-simplex parameterization of the compositional space. We study the behavior of thermal-compositional reservoir displacement processes across a wide range of fluid mixtures, pressures, and temperatures. We show that our approach rigorously accounts for tie-simplex degeneration across phase boundaries. We also focus on the complex behavior of the tie-triangles and tie-lines associated with three-phase, steam injection problems in heterogeneous formations. Our studies indicate that the tie-simplex based simulation is a potential approach for fast EOS modeling of complex EOR processes.


Author(s):  
Theodoros Tsoulos ◽  
Supriya Atta ◽  
Maureen Lagos ◽  
Michael Beetz ◽  
Philip Batson ◽  
...  

<div>Gold nanostars display exceptional field enhancement properties and tunable resonant modes that can be leveraged to create effective imaging tags or phototherapeutic agents, or to design novel hot-electron based photocatalysts. From a fundamental standpoint, they represent important tunable platforms to study the dependence of hot carrier energy and dynamics on plasmon band intensity and position. Toward the realization of these platforms, holistic approaches taking into account both theory and experiments to study the fundamental behavior of these</div><div>particles are needed. Arguably, the intrinsic difficulties underlying this goal stem from the inability to rationally design and effectively synthesize nanoparticles that are sufficiently monodispersed to be employed for corroborations of the theoretical results without the need of single particle experiments. Herein, we report on our concerted computational and experimental effort to design, synthesize, and explain the origin and morphology-dependence of the plasmon modes of a novel gold nanostar system, with an approach that builds upon the well-known plasmon hybridization model. We have synthesized monodispersed samples of gold nanostars with finely tunable morphology employing seed-mediated colloidal protocols, and experimentally observed narrow and spectrally resolved harmonics of the primary surface plasmon resonance mode both at the single particle level (via electron energy loss spectroscopy) and in ensemble (by UV-Vis and ATR-FTIR spectroscopies). Computational results on complex anisotropic gold nanostructures are validated experimentally on samples prepared colloidally, underscoring their importance as ideal testbeds for the study of structure-property relationships in colloidal nanostructures of high structural complexity.</div>


2018 ◽  
Vol 55 (3) ◽  
pp. 252-257 ◽  
Author(s):  
Derong Xu ◽  
Wanli Kang ◽  
Liming Zhang ◽  
Jiatong Jiang ◽  
Zhe Li ◽  
...  

2021 ◽  
Vol 35 (4) ◽  
pp. 3011-3031
Author(s):  
Ali Esfandiarian ◽  
Ali Maghsoudian ◽  
Mahsa Shirazi ◽  
Yousef Tamsilian ◽  
Shahin Kord ◽  
...  

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Marcos L. Corazza ◽  
Julia Trancoso

Abstract The search for sustainable ideas has gained prominence in recent decades at all levels of society since it has become imperative an economic, social, and environmental development in an integrated manner. In this context, biorefineries are currently present as the technology that best covers all these parameters, as they add the benefits of waste reuse, energy cogeneration, and fossil fuel substitution. Thus, the study of the various applicable biological matrices and exploring the technical capabilities of these processes become highly attractive. Thermodynamic modeling acts in this scenario as a fundamental tool for phase behavior predictions in process modeling, design, and optimization. Thus, this work aimed to systematize, using the PRISMA statement for systematic reviews, the information published between 2010 and 2020 on phase equilibria modeling in systems related to biorefineries to organize what is already known about the subject. As a result, 236 papers were categorized in terms of the year, country, type of phase equilibria, and thermodynamic model used. Also, the phase behavior predictions of different thermodynamic models under the same process conditions were qualitatively compared, establishing PC-SAFT as the model that best represents the great diversity of interest systems for biorefineries in a wide range of conditions.


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