scholarly journals Growing Interface with Phase Separation and Spontaneous Convection during Hydrodynamically Stable Displacement

Materials ◽  
2021 ◽  
Vol 14 (20) ◽  
pp. 6089
Author(s):  
Takahiko Ban ◽  
Ryohei Tanaka ◽  
Ryuta X. Suzuki ◽  
Yuichiro Nagatsu

The displacement of one fluid by another is an important process, not only in industrial and environmental fields, such as chromatography, enhanced oil recovery, and CO2 sequestration, but also material processing, such as Lost Foam Casting. Even during hydrodynamically stable fluid displacement where a more viscous fluid displaces a less viscous fluid in porous media or in Hele-Shaw cells, the growing interface fluctuates slightly. This fluctuation is attributed to thermodynamic conditions, which can be categorized as the following systems: fully miscible, partially miscible, and immiscible. The dynamics of these three systems differ significantly. Here, we analyze interfacial fluctuations under the three systems using Family–Vicsek scaling and calculate the scaling indexes. We discovered that the roughness exponent, , and growth exponent, , of the partially miscible case are larger than those of the immiscible and fully miscible cases due to the effects of the Korteweg convection as induced during phase separation. Moreover, it is confirmed that fluctuations in all systems with steady values of and are represented as a single curve, which implies that accurate predictions for the growing interface with fluctuations in Hele-Shaw flows can be accomplished at any scale and time, regardless of the miscibility conditions.

Coatings ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 960
Author(s):  
Ryuta X. Suzuki ◽  
Risa Takeda ◽  
Yuichiro Nagatsu ◽  
Manoranjan Mishra ◽  
Takahiko Ban

The displacement of a less viscous fluid by a more viscous fluid in a radial Hele-Shaw cell makes a circular pattern because the interface is hydrodynamically stable in this condition. Very recently, it has been experimentally reported that the hydrodynamically stable displacement in a partially miscible system induces fingering patterns while stable circular patterns are made at fully miscible and immiscible systems. The fingering instability in the partially miscible system results from complex and entangled elements involving viscous dissipation, molecular diffusion, and phase separation. The analyzing mechanism requires a quantitative relationship between the hydrodynamic interfacial fingering patterns and underlying physicochemical properties. Here, we experimentally investigated the change in fluid patterns formed by the progression of phase separation in the partially miscible systems and categorized them into three patterns: finger-like pattern, annular-like pattern, and circular pattern. Moreover, we propose the mechanism of the pattern formation by an interfacial tension measurement and evaluate the patterns by modified capillary number and newly defined body force ratio, Bf. Our analysis revealed that the deformation index of the pattern can be expressed as a function of Bf on a single curve regardless of the miscibility.


2021 ◽  
Author(s):  
Rukaun Chai ◽  
Yuetian Liu ◽  
Qianjun Liu ◽  
Xuan He ◽  
Pingtian Fan

Abstract Unconventional reservoir plays an increasingly important role in the world energy system, but its recovery is always quite low. Therefore, the economic and effective enhanced oil recovery (EOR) technology is urgently required. Moreover, with the aggravation of greenhouse effect, carbon neutrality has become the human consensus. How to sequestrate CO2 more economically and effectively has aroused wide concerns. Carbon Capture, Utilization and Storage (CCUS)-EOR is a win-win technology, which can not only enhance oil recovery but also increase CO2 sequestration efficiency. However, current CCUS-EOR technologies usually face serious gas channeling which finally result in the poor performance on both EOR and CCUS. This study introduced CO2 electrochemical conversion into CCUS-EOR, which successively combines CO2 electrochemical reduction and crude oil electrocatalytic cracking both achieves EOR and CCUS. In this study, multiscale experiments were conducted to study the effect and mechanism of CO2 electrochemical reduction for CCUS-EOR. Firstly, the catalyst and catalytic electrode were synthetized and then were characterized by using scanning electron microscope (SEM) & energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). Then, electrolysis experiment & liquid-state nuclear magnetic resonance (1H NMR) experiments were implemented to study the mechanism of CO2 electrochemical reduction. And electrolysis experiment & gas chromatography (GC) & viscosity & density experiments were used to investigate the mechanism of crude oil electrocatalytic cracking. Finally, contact angle and coreflooding experiments were respectively conducted to study the effect of the proposed technology on wettability and CCUS-EOR. SEM & EDS & XPS results confirmed that the high pure SnO2 nanoparticles with the hierarchical, porous structure, and the large surface area were synthetized. Electrolysis & 1H NMR experiment showed that CO2 has converted into formate with the catalysis of SnO2 nanoparticles. Electrolysis & GC & Density & Viscosity experiments indicated that the crude oil was electrocatalytically cracked into the light components (<C20) from the heavy components (C21∼C37). As voltage increases from 2.0V to 7.0V, the intensity of CO2 electrocchemical reduction and crude oil electrocatalytic cracking enhances to maximum at 3.5V (i.e., formate concentration reaches 6.45mmol/L and carbon peak decreases from C17 to C15) and then weakens. Contact angle results indicated that CO2 electrochemical reduction and crude oil electocatalytic cracking work jointly to promote wettability alteration. Thereof, CO2 electrochemical reduction effect is dominant. Coreflooding results indicated that CO2 electrochemical reduction technology has great potential on EOR and CCUS. With the SnO2 catalytic electrode at optimal voltage (3.5V), the additional recovery reaches 9.2% and CO2 sequestration efficiency is as high as 72.07%. This paper introduced CO2 electrochemical conversion into CCUS-EOR, which successfully combines CO2 electrochemical reduction and crude oil electrocatalytic cracking into one technology. It shows great potential on CCUS-EOR and more studies are required to reveal its in-depth mechanisms.


Processes ◽  
2018 ◽  
Vol 6 (10) ◽  
pp. 178 ◽  
Author(s):  
Richeng Liu ◽  
Yujing Jiang

The fluid flow in fractured porous media plays a significant role in the characteristic/assessment of deep underground reservoirs such as CO2 sequestration [1–3], enhanced oil recovery [4,5] and geothermal energy development [...]


2021 ◽  
Author(s):  
Rukuan Chai ◽  
Yuetian Liu ◽  
Yuting He ◽  
Qianjun Liu ◽  
Wenhuan Gu

Abstract Tight oil reservoir plays an increasingly important role in the world energy system, but its recovery is always so low. Hence, a more effective enhanced oil recovery (EOR) technology is urgently needed. Meanwhile, greenhouse effect is more and more serious, a more effective carbon capture and sequestration (CCS) method is also badly needed. Direct current voltage assisted carbonated water-flooding is a new technology that combines direct current voltage with carbonated water-flooding to enhance oil recovery and CO2 sequestration efficiency, simultaneously. Experimental studies were conducted from macroscopic-scale to microscopic-scale to study the performance and mechanism of direct current voltage assisted carbonated water-flooding. Firstly, core flood experiments were implemented to study the effect of direct current voltage assisted carbonated water on oil recovery and CO2 sequestration efficiency. Secondly, contact angle and interfacial tension/dilatational rheology were measured to analyze the effect of direct current voltage assisted carbonated water on crude oil-water-rock interaction. Thirdly, total organic carbon (TOC), gas chromatography (GC), and electrospray ionization-fourier transform ion cyclotron resonance-mass spectrometry (ESI FT ICR-MS) were used to investigate the organic composition change of produced effluents and crude oil in direct current voltage assisted carbonated water treatment. Through direct current voltage assisted carbonated water-flooding experiments, the following results can be obtained. Firstly, direct current voltage assisted carbonated waterflooding showed greater EOR capacity and CO2 sequestration efficiency than individual carbonated water and direct current voltage treatment. With the increase of direct current voltage, oil recovery increases to 38.67% at 1.6V/cm which much higher than 29.07% of carbonated water-flooding and then decreases, meanwhile, CO2 output decreases to only 35.5% at 1.6V/cm which much lower than 45.6% of carbonated water-flooding and then increases. Secondly, in direct current voltage assisted carbonated water-flooding, the wettability alteration is mainly caused by carbonated water and the effect of direct current can be neglected. While both carbonated water and direct current have evident influence on interfacial properties. Herein, with direct current voltage increasing, the interfacial tension firstly decreases and then increases, the interfacial viscoelasticity initially strengthens and then weakens. Thirdly, GC results indicated that crude oil cracking into lighter components occurs during direct current voltage assisted carbonated water-flooding, with the short-chain organic components increasing and the long-chain components decreasing. Meanwhile, TOC and ESI FT ICR-MS results illustrated that CO2 electroreduction do occur in direct current voltage assisted carbonated water-flooding with the dissolved organic molecules increases and the emergence of formic acid. Conclusively, the synergy of CO2 electrochemical reduction into formic acid in aqueous solution and the long-chain molecules electrostimulation pyrolysis into short ones in crude oil mutually resulted in the enhancement of crude oil-carbonated water interaction. This paper proposed a new EOR & CCS technology-direct current voltage assisted carbonated water-flooding. It showed great research and application potential on tight oil development and greenhouse gas control. More work needs to be done to further explore its mechanism. This paper constructs a multiscale & interdisciplinary research system to study the multidisciplinary (EOR&CCS) problem. Specifically, a series connected physical (Core displacement, Contact angle, and Interfacial tension/rheology measurements) and chemistry (TOC, GS, and ESI FT ICR-MS) experiments are combined to explore its regularity and several physics (Atomic physics) and chemistry (Electrochemistry/Inorganic Chemistry) theories are applied to explain its mechanisms.


2014 ◽  
Vol 63 ◽  
pp. 7685-7693 ◽  
Author(s):  
Zhenxue Dai ◽  
Hari Viswanathan ◽  
Julianna Fessenden-Rahn ◽  
Richard Middleton ◽  
Feng Pan ◽  
...  

2020 ◽  
Vol 60 (2) ◽  
pp. 662
Author(s):  
Saira ◽  
Furqan Le-Hussain

Oil recovery and CO2 storage related to CO2 enhance oil recovery are dependent on CO2 miscibility. In case of a depleted oil reservoir, reservoir pressure is not sufficient to achieve miscible or near-miscible condition. This extended abstract presents numerical studies to delineate the effect of alcohol-treated CO2 injection on enhancing miscibility, CO2 storage and oil recovery at immiscible and near-miscible conditions. A compositional reservoir simulator from Computer Modelling Group Ltd. was used to examine the effect of alcohol-treated CO2 on the recovery mechanism. A SPE-5 3D model was used to simulate oil recovery and CO2 storage at field scale for two sets of fluid pairs: (1) pure CO2 and decane and (2) alcohol-treated CO2 and decane. Alcohol-treated CO2 consisted of a mixture of 4 wt% of ethanol and 96 wt% of CO2. All simulations were run at constant temperature (70°C), whereas pressures were determined using a pressure-volume-temperature simulator for immiscible (1400 psi) and near-miscible (1780 psi) conditions. Simulation results reveal that alcohol-treated CO2 injection is found superior to pure CO2 injection in oil recovery (5–9%) and CO2 storage efficiency (4–6%). It shows that alcohol-treated CO2 improves CO2 sweep efficiency. However, improvement in sweep efficiency with alcohol-treated CO2 is more pronounced at higher pressures, whereas improvement in displacement efficiency is more pronounced at lower pressures. The proposed methodology has potential to enhance the feasibility of CO2 sequestration in depleted oil reservoirs and improve both displacement and sweep efficiency of CO2.


2010 ◽  
Vol 13 (05) ◽  
pp. 791-804 ◽  
Author(s):  
Ian Taggart

Summary The solubility of carbon dioxide (CO2) in underground saline formations is considered to offer significant long-term storage capability to effectively sequester large amounts of anthropogenic CO2. Unlike enhanced oil recovery (EOR), geosequestration relies on longer time scales and involves significantly greater volumes of CO2. Many geosequestration studies assume that the initial brine state is one containing no dissolved hydrocarbons and, therefore, apply simplistic two-component solubility models starting from a zero dissolved-gas state. Many brine formations near hydrocarbons, however, tend to be close to saturation by methane (CH4). The introduction of excess CO2 in such systems results in an extraction of the CH4 into the CO2-rich phase, which, in turn, has implications for monitoring of any sequestration project and offers the possibly additional CH4 mobilization and recovery.


2015 ◽  
Vol 26 (10) ◽  
pp. 1550115
Author(s):  
Palash Nath ◽  
Debnarayan Jana

In this present numerical work, we report a discrete erosion kind of model in (1 + 1)-dimension. Erosion and re-deposition phenomena with probabilities p and q(= 1 - p) are considered as two tunable parameters, which control the overall kinetic roughening behavior of the interface. Redeposition or diffusion dominated erosion like kinetic roughening model gives rise to nonuniversal growth exponent, which varies continuously with respect to erosion probability. However, universal character is restored for the roughness exponent with the value of 0.5 in (1 + 1)-dimension with respect to p. Due to nonuniversal nature of growth exponent, we observe a significant modification to the scaling behavior of surface width with respect to erosion probability. For low erosion probability (≲ 0.1) a power law like divergence has been observed of the correlation growth time. This can be argued as limiting behavior of a generalized functional behavior of crossover time with erosion probability.


2017 ◽  
Vol 114 ◽  
pp. 6957-6967 ◽  
Author(s):  
Zhenxue Dai ◽  
Hari Viswanathan ◽  
Ting Xiao ◽  
Richard Middleton ◽  
Feng Pan ◽  
...  

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